diff --git a/data/38/00/B2/3800B2819E78453D93DAA5440B9AF549.xml b/data/38/00/B2/3800B2819E78453D93DAA5440B9AF549.xml new file mode 100644 index 00000000000..267ced05b0a --- /dev/null +++ b/data/38/00/B2/3800B2819E78453D93DAA5440B9AF549.xml @@ -0,0 +1,201 @@ + + + +The genus Mercuria Boeters, 1971 in Morocco: first molecular phylogeny of the genus and description of two new species (Caenogastropoda, Truncatelloidea, Hydrobiidae) + + + +Author + +Boulaassafer, Khadija + + + +Author + +Ghamizi, Mohamed + + + +Author + +Delicado, Diana + +text + + +ZooKeys + + +2018 + +782 + + +95 +128 + + + + +http://dx.doi.org/10.3897/zookeys.782.26797 + +journal article +http://dx.doi.org/10.3897/zookeys.782.26797 +1313-2970-782-95 +2B276BC250E94244A32A524E2B266DB3 + + + + + +Mercuria targouasensis +Gloeer +, Boeters & Walther, 2015 + + + + + +Mercuria confusa +Backhuys & Boeters, 1974: 113 + + + +Material. + +Examined material. MOROCCO. MHNM 18 ZTMH10, UGSB 17912, Oum Rbii Springs, N of Khenifera, 01/06/2015 ( +33°3.2059'N +, +5°24.8797'W +); MHNM 18 ZTMH11, UGSB 17955, a small ditch in Mirleft, 02/02/2015 ( +29°35.0167'N +, +10°1.845'W +). + + + +Revised diagnosis. + +Shell ovate-conic, whorls 3-5; periostracum whitish; body whorl occupying more than three-quarters of total shell length; aperture ovate; umbilicus narrow, partially covered by the inner lip; operculum brownish to slightly orange; central radular tooth formula 3 +-C-3/1- +1; bursa copulatrix elongate, with a short duct; one seminal receptacle pyriform, with a short duct; penis gradually tapering, grey; penial appendix shorter than penis, grey, base wide, medially positioned on inner edge of penis; nervous system extremely elongated (mean RPG ratio = 0.70), gently black pigmented. + + + +Description. + +Shell ovate-conic, whorls 3-5, height 2.63-3.43 mm (Figure 7 +A-C +; Suppl. material 1: Table 1). Periostracum whitish. Protoconch with two whorls, diameter ca. 600 +µm +; nucleus ca. 140 +µm +wide (Figure 7H); protoconch microsculpture granulated (Figure 7I). Teleoconch whorls convex, separated by deep sutures. Body whorl large, occupying three-quarters of total shell length. Aperture ovate, complete, in contact with the body whorl; inner lip thicker than outer lip; peristome margin straight (Figure 7D, E). Umbilicus narrow, partially covered by the inner lip. + + + +Figure 7. Shells and opercula, +M. targouasensis +. A, B, E Shell, Oum Rbii Springs C, D Shell, a small ditch in Mirleft F, G Opercula (inner, outer sides), Oum Rbii Springs H, I Protoconch and detailed microsculpture of protoconch, Oum Rbii Springs. + + + +Operculum as for genus, light orange to brown, whorls 2; muscle attachment area near nucleus (Figure 7F, G). Radula length intermediate, ca. 800 +µm +long (20% total shell length), seven times longer than wide, with approx. 50 rows of teeth (Fig. 8A; Suppl. material 1: Table 2). Central tooth formula 3 +-C-3/1- +1; central cusp tapered, long. Lateral teeth formula (4)3 +-C- +3(4); central cusp wide, V-shaped (Figure 8B, +D-F +). Inner and outer marginal teeth having 11-15 and 14-18 cusps, respectively (Figure 8C, F). + + + +Figure 8. Radulae, +M. targouasensis +. +A-D +Oum Rbii Springs E, F A small ditch in Mirleft. A Radular ribbon B, E Central tooth C, D, F Inner marginal, outer marginal, and lateral teeth. + + + +Animal black pigmented except for pale area surrounding eye lobes and neck (Figure 9G, H). Ctenidium well-developed, with 19-25 gill filaments, occupying almost entire length of the pallial cavity. Osphradium elongate, positioned approximate middle of ctenidium (Figure 9A). Stomach nearly as long as wide; style sac slightly shorter than stomach, surrounded by an unpigmented intestine (Figure 9B; Suppl. material 1: Table 3). Glandular oviduct three times longer than wide. Capsule gland longer and thicker than +albumen +gland. Bursa copulatrix pyriform to elongate, with a short duct. Renal oviduct unpigmented, coiled, making three loops. Seminal receptacle pyriform, with a short duct, joining renal oviduct above the insertion point with bursal duct (Figure 9D, E; Suppl. material 1: Table 4). Prostate gland bean-shaped, ca. 2.5 times longer than wide (Figure 9F; Suppl. material 1: Table 5); seminal duct entering the posterior region; pallial vas deferens emerging close to its anterior edge. Penis gradually tapering, attached to the area close to the right eye. Penial appendix slightly pigmented, shorter than penis, base wide, middle positioned on inner edge of penis. Terminal gland large, occupying the whole distal end of the appendix (Figure 9 +G-J +; Suppl. material 1: Table 5). Nervous system gently pigmented, extremely elongated (mean RPG ratio = 0.70; Suppl. material 1: Table 6); cerebral ganglia equal in size and shape (Figure 9C). + + + +Figure 9. Anatomical structures, +M. targouasensis +. +A-F +, H A small ditch in Mirleft G, +I-J +Oum Rbii Springs. A Ctenidium B Stomach C Partial nervous system D Pallial oviduct E Bursa copulatrix and seminal receptacle F Prostate gland G, H Head with penis I, J Head and penis drawings. RO renal oviduct SR seminal receptacle. + + + + +Distribution. +This species was found in coastal streams in southwestern Morocco and in a spring-fed habitat in the Middle Atlas. + + +Remarks. + +The morphological and anatomical descriptions presented here are based on specimens collected at two sites: one in the Mirleft region, 70 km from the +type +locality, (i.e., ford Oued Assaka), and another, in a more remote place in the Middle Atlas Mountains. The population collected in the surroundings of Mirleft may correspond to the species +Mercuria +'mirlheftensis' +(nomen nudum) from the same area suggested by + +Garcia +et al. (2010) + +. However, the name +M. +'mirlheftensis' +is not valid. Specimens collected in the Mirleft area resemble specimens from the type locality of +M. targouasensis +regarding the shape of the penis and prostate, and also of the female genitalia, especially bursa copulatrix shape. Based on the geographic proximity of these two localities and the similarity in shell and anatomical characters of their specimens, we assigned the population from Mirleft to +M. targouasensis +. Specimens from Oum +Rbii +(Middle Atlas) were also tentatively assigned to this species based on shell and morphological similarities and a short genetic distance (1.3%) between this and the Mirleft population. However, this assignment needs confirmation in future systematic studies on +Mercuria +, which should include these and other Mediterranean species. + + +Mercuria targouasensis +and +M. midarensis +sp. n. are sister species and differ molecularly by 2.1%-3.4% (mean sequence divergence 2.8%). The two species are close in shell dimensions but differ in other shell features such as the relative size of the body +whorl +(larger in +M. targouasensis +) or the umbilicus (wider in +M. midarensis +sp. n.). They also differ anatomically; +Mercuria midarensis +sp. n. has typically a strap-like penis, 2.5 times longer than head length, a small penial appendix with narrow insertion into the penis, and an elongate bursa copulatrix, whereas in +M. targouasensis +, the penis is more often gradually tapering, equal or 1.5 times longer than head length, the penial appendix is larger with a wider insertion, and the bursa copulatrix is pyriform to elongate. These two species also differ in the number of cusps on radular teeth (Suppl. material 1: Table 2). + + + +Ecology. + +In the new localities of +M. targouasensis +, this species was found attached to stones in a saltwater spring in the Middle Atlas (ca. 1,200 m a.s.l. altitude, and 37.9 PSU, practical salinity unit) and in the sediment of a ditch in the region of Mirleft cohabiting with +Melanopsis praemorsa +. + + + + \ No newline at end of file diff --git a/data/38/01/A2/3801A27538C7A680C2CAD744BB4BD968.xml b/data/38/01/A2/3801A27538C7A680C2CAD744BB4BD968.xml new file mode 100644 index 00000000000..470421bf34b --- /dev/null +++ b/data/38/01/A2/3801A27538C7A680C2CAD744BB4BD968.xml @@ -0,0 +1,226 @@ + + + +Neoprotoparmelia gen. nov. and Maronina (Lecanorales, Protoparmelioideae): species description and generic delimitation using DNA barcodes and phenotypical characters + + + +Author + +Singh, Garima + + + +Author + +ptroot, Andre + + + +Author + +ico, Victor J. + + + +Author + +tte, Juergen + + + +Author + +Pradeep K. Divakar, + + + +Author + +Crespo, Ana + + + +Author + +Caceres, Marcela Eugenia da Silva + + + +Author + +H. Thorsten Lumbsch, + + + +Author + +Schmitt, Imke + +text + + +MycoKeys + + +2018 + +44 + + +19 +50 + + + + +http://dx.doi.org/10.3897/mycokeys.44.29904 + +journal article +http://dx.doi.org/10.3897/mycokeys.44.29904 +1314-4049--19 + + + + +Neoprotoparmelia pauli V. J. Rico, Lumbsch & Garima Singh +sp. nov. +Figure 11 + + + +Type. + +KENYA. Eastern Prov., Mwingi Co., Nuu Hill, +01°02'S +, +38°20'E +, ca. 1000 m alt., inselberg with dry woodland dominated by Terminalia, +Combretum +and +Acacia +, on sandstone, 12 March 2014, P.M. Kirika & H.T. Lumbsch 3821 (holotype: EA, isotype: F). + + + +Figure 11. +Neoprotoparmelia pauli +, holotype Kirika & Lumbsch 3821 (EA) a Habit b Centre of apothecia section, showing cupular proper exciple (arrow). Scale bars: 1 mm (a), 20 +µm +(b). + + + + +Diagnosis. + +Similar to +Neoprotoparmelia capensis +but differs from it by having a reduced, olive tinged thallus and smaller apothecia. Moreover, the major secondary metabolite produced by +Neoprotoparmelia pauli +is +α-collatolic +acid, absent in +N. capensis +. + + + +Etymology. +The new species is named after our colleague, the Kenyan lichenologist, Paul M. Kirika, who was one of the collectors of the type material. + + +Description. + +Thallus saxicolous, crustose, up to 3 cm wide, rimose to areolate, thin (up to 0.8 mm thick); surface dark brown, olive-brown to light olive-brown, sometimes with whitish mottled-fissured areas (by a locally strong mucilaginous epicortex), dull to slightly shiny; blackish hypothalline line blackish or absent. Areoles irregular, polygonal to rounded, up to 0.75(-1.2) mm in diam., flat to slightly convex, surface mainly smooth, marginal areoles sometimes lobe-like. Apothecia frequent, 1 per areolae, zeorine to lecanorine, mainly immersed and nearly urceolate or adnate, rounded, up to 0.4 mm in diam.; disc brown to brown-black, dull, concave to flat; thalline exciple persistent, concolorous with thallus to whitish (by a strong mucilaginous epicortex); proper exciple cupulate, up to 35 +µm +thick, coherent, hyphae mainly periclinal with strong mucilaginous walls. Hymenium hyaline, coherent, 35-60 +µm +tall; epihymenium light brown to brown, up to 15 +µm +tall, with few irregular granules; hypothecium and subhymenium hyaline, 15-35 +µm +thick. Paraphyses coherent in water, branched and anastomosed, apices somewhat thickened and mainly surrounded by a brown mucilaginous hood (up to 7.5 +µm +wide). Asci clavate, 50 +x +16 +µm +, 8-spored, amyloid tholus (excluding the axial mass) and surrounding mucilage, +Lecanora +-type (cf. also +Maronina +-type, +Kantvilas et al. 2010 +). Ascospores hyaline, simple, 10-12.5 +x +4-5 +µm +(n = 8), fusiform to elongate (l:b = 2-2.75), with rounded apices or sometimes slightly apiculate in one end, some with apical hyaline setae. Pycnidia immersed, globose to oblong, wall hyaline, ostiole tissue with brown pigmented walls. Conidia simple, hyaline, (9 +-)10- +17 +x +1-1.5 +µm +(n = 20), bacilliform, straight. + + + +Chemistry. + +Spot tests: medulla +K- +or ++/- +unclean yellowish, +C- +, +KC- +, +I- +, +P- +, UV+ greenish-white. TLC: atranorin (minor or traces), +α-collatolic +acid (major or minor), +α-alectoronic +acid (minor), unidentified substance (major or traces, closed to norstictic acid, Rf class 4), ++/- +β-alectoronic +(traces) and traces of related substances. + + + +Distribution and ecology. + +Only known from the type locality in Kenya, covered with upland dry forest ecosystems ( +Wass 1995 +), growing on exposed sandstones. + + + +Reference sequences. +(specimen: Kirika & Lumbsch 3821, holotype: EA). KP822469 (mtSSU), KP822279 (ITS), KP796348 (nuLSU), KP822148 (RPB1), KP823526 (TSR1). + + +Remarks. + +Consists of specimens recovered within ' +P. +sp. +KE' +in ' +Protoparmelia +tropical +clade' +in +Singh et al. (2015) +, supported as an evolutionary independent lineage based on the coalescent-based species delimitation analysis. The thalli of the type material were poorly developed, immature apothecia and only a few mature spores were found. This hindered us in providing detailed morphological features (especially ascomatal) and thus future collections may slightly change the morphological description. Its olive-brown thalli, 8-spored asci, +α-collatolic +acid presence, distribution and/or molecular data supports it as an evolutionary independent lineage from the other two saxicolous +Neoprotoparmelia +species. + + + + \ No newline at end of file diff --git a/data/38/01/E3/3801E359ABF75384974B315EF91DAE7F.xml b/data/38/01/E3/3801E359ABF75384974B315EF91DAE7F.xml new file mode 100644 index 00000000000..b89abf778df --- /dev/null +++ b/data/38/01/E3/3801E359ABF75384974B315EF91DAE7F.xml @@ -0,0 +1,107 @@ + + + +Revision and phylogeny of the genus Loxoneptera Hampson, 1896 (Lepidoptera, Crambidae, Pyraustinae), based on morphology and molecular data + + + +Author + +Xiang, Lanbin +School of Life Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510275, China + + + +Author + +Chen, Kai +School of Life Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510275, China + + + +Author + +Zhang, Dandan +School of Life Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510275, China & School of Ecology, Sun Yat-sen University, Guangzhou, Guangdong 510275, China +zhdd61@163.com + +text + + +ZooKeys + + +2021 + +2021-05-05 + + +1036 + + +75 +98 + + + + +http://dx.doi.org/10.3897/zookeys.1036.63814 + +journal article +http://dx.doi.org/10.3897/zookeys.1036.63814 +1313-2970-1036-75 +B6A437B0E1B54E67B52653084C5185FE +C84501F710F75030AD2C010EE307414D + + + + +Loxoneptera brevipalpis (Snellen, 1890) +comb. nov. +Figs 12 +, 24 + + + + +Calamochrous brevipalpis +Snellen, 1890: 599. + + + +Material examined. + + +Type material +. + +Holotype +, + +, Sikkim, O. +Moeller +, +Pyralidae +Brit. Mus. Slide No. 9748 (NHMUK). + + + +Diagnosis. + +Wingspan 33.0 mm. This species is distinguished by dull luteous forewing suffused with ochreous scales and bearing indistinct orbicular and reniform stigmata, lustrous hindwing suffused with grey scales along the costa. In the male genitalia, this species is similar to + +L. dichroma + +in the shape of the dorsal projection of the transtilla, ventral sella and valva, as well as by the process of dorso-distal sella extended ventrad and beyond the ventral margin of valva. + +Loxoneptera brevipalpis + +can be distinguished by the thick and heavily sclerotised process of dorso-distal sella, and the heavily sclerotised, spiny, thumb-shaped cornutus. + + + +Distribution. +India (Sikkim). + + + \ No newline at end of file diff --git a/data/38/02/0C/38020C0E86AE865E48AE93C0B6549E15.xml b/data/38/02/0C/38020C0E86AE865E48AE93C0B6549E15.xml new file mode 100644 index 00000000000..fa9b0b3d694 --- /dev/null +++ b/data/38/02/0C/38020C0E86AE865E48AE93C0B6549E15.xml @@ -0,0 +1,90 @@ + + + +Birds from the Azores: An updated list with some comments on species distribution + + + +Author + +Barcelos, Luis MD + + + +Author + +Rodrigues, Pedro R + + + +Author + +Bried, Joel + + + +Author + +Mendonca, Enesima P + + + +Author + +Gabriel, Rosalina + + + +Author + +Borges, Paulo Alexandre Vieira + +text + + +Biodiversity Data Journal + + +2015 + +3 + + +6604 +6604 + + + + +http://dx.doi.org/10.3897/BDJ.3.e6604 + +journal article +http://dx.doi.org/10.3897/BDJ.3.e6604 +1314-2828-3-6604 + + + + +Milvus milvus (Linnaeus, 1758) + + + +Ecological interactions + +Native status +Palearctic + + + +Distribution +COR; SMG + + +Notes + +Occasional Migrant. +Rodrigues et al. (2010) + + + + \ No newline at end of file diff --git a/data/38/02/59/3802590CFE11643529C1FBA3FF54E894.xml b/data/38/02/59/3802590CFE11643529C1FBA3FF54E894.xml new file mode 100644 index 00000000000..be846996717 --- /dev/null +++ b/data/38/02/59/3802590CFE11643529C1FBA3FF54E894.xml @@ -0,0 +1,164 @@ + + + +Four new species of Isoneuromyia from China (Diptera: Keroplatidae) + + + +Author + +Xu, Huachao + + + +Author + +Cao, Jian + + + +Author + +Wu, Hong + + + +Author + +Evenhuis, Neal L. + + + +Author + +Zhou, Zuji + +text + + +Zootaxa + + +2007 + +1423 + + +51 +57 + + + +journal article +10.5281/zenodo.175701 +e41d47ba-2b34-4952-a9a5-08731dd08567 +1175-5326 +175701 + + + + + + + +Isoneuromyia wolongensis +Xu, Cao et Evenhuis + +, +n. sp. + + + + +( +Figs. 4, 8 +, +13 +) + + + + +Diagnosis. +Closest to + +I. singula + +, +n. sp. +but can be distinguished from it by the gonostyli having two dark teeth (only one in + +singula + +). + + + + +Description. +MALE. Lengths: Body: +8.5 mm +; wing: +5.6mm +. + + +Head +. Vertex and occiput black, with fairly dense small black recumbent hairs. Ocelli in horizontal line. Frons light brown, bare. Antennae: scape and pedicel cup-shaped, brownish black. Flagellum: segments slightly compressed, brownish black. Face light brown, with small black hairs apicolaterally. Palpi brown. Proboscis yellowish brown. + + +Thorax +. Mesonotum ( +Fig. 4 +) black, pruinose with brown bristles. Scutellum black. Patch of thick black setae above wing root and on posterior margin of scutellum. Prescutellar area tapering to scutellum. Pronotal lobes black with dense black setae. Pleura, laterotergite and mediotergite brownish black, bare. Halter yellow. + + +Legs +. Fore coxa brownish, mid and hind coxae with brown spot at base; fore coxa, and apex of mid and hind coxa, with recumbent black hairs. Fore and mid femora brownish black at base, remainder of them yellow; hind femur brown, all with recumbent black hairs. Fore tibia without comb, mid with only posterior comb, hind tibiae with anterior and posterior comb. Tibial spurs black. Fore and mid basitarsus subequal in length to lengths of respective tibiae, hind basitarsus 0.9x length of hind tibia. Claws minute. + + +Wing +( +Fig. 8 +). Hyaline, with brown infuscation subapically from costa to middle of cell r5, fading posteriorly; vein R4 straight, ending in C slightly beyond end of R1; veins M2, CuA1 and A1 not reaching wing margin. + + +Abdomen +. Tergites I–II black; tergites III–VI brownish black with white spots basolaterally; tergites V– VII brownish black, tergite VIII brown, all tergites with dense recumbent black hairs. Sternites patterned as on tergites. + + +Hypopygium +( +Fig. 13 +). Not dissected. Gonocoxites brownish, black pilose on about apical half. Gonostyli brown, black pilose, apex with two dark teeth, two minute dark sclerotized tooth in between large darkly sclerotized teeth. + +FEMALE. Unknown. + + +Types +. + +Holotype +ɗ (ZJFC +060200 +) and +paratype +ɗ from: +China +: Sichuan province: Wolong National Natural Reserve, +21 July 2006 +, Jian Cao. + + + + +Etymology. +The species epithet derives from the place name +Wolong +, referring to the +type +locality of the species. + + + + \ No newline at end of file diff --git a/data/38/02/59/3802590CFE12643529C1FE5BFF44EBBA.xml b/data/38/02/59/3802590CFE12643529C1FE5BFF44EBBA.xml new file mode 100644 index 00000000000..dd5ac0156f0 --- /dev/null +++ b/data/38/02/59/3802590CFE12643529C1FE5BFF44EBBA.xml @@ -0,0 +1,81 @@ + + + +Four new species of Isoneuromyia from China (Diptera: Keroplatidae) + + + +Author + +Xu, Huachao + + + +Author + +Cao, Jian + + + +Author + +Wu, Hong + + + +Author + +Evenhuis, Neal L. + + + +Author + +Zhou, Zuji + +text + + +Zootaxa + + +2007 + +1423 + + +51 +57 + + + +journal article +10.5281/zenodo.175701 +e41d47ba-2b34-4952-a9a5-08731dd08567 +1175-5326 +175701 + + + + + + + +Isoneuromyia semirufa +Meigen, 1818 + + + + + + + +Material examined: +China +: Zhejiang province: Wuyanling National Natural Reserve, 1ɗ, +4 May 2006 +, Yiping Wang. + + + + \ No newline at end of file diff --git a/data/38/02/59/3802590CFE15643229C1FF33FA3DEA19.xml b/data/38/02/59/3802590CFE15643229C1FF33FA3DEA19.xml new file mode 100644 index 00000000000..d798342fb98 --- /dev/null +++ b/data/38/02/59/3802590CFE15643229C1FF33FA3DEA19.xml @@ -0,0 +1,181 @@ + + + +Four new species of Isoneuromyia from China (Diptera: Keroplatidae) + + + +Author + +Xu, Huachao + + + +Author + +Cao, Jian + + + +Author + +Wu, Hong + + + +Author + +Evenhuis, Neal L. + + + +Author + +Zhou, Zuji + +text + + +Zootaxa + + +2007 + +1423 + + +51 +57 + + + +journal article +10.5281/zenodo.175701 +e41d47ba-2b34-4952-a9a5-08731dd08567 +1175-5326 +175701 + + + + + + +Key to the species of + +Isoneuromyia +Brunetti + +known from +China + + + + + + + +1. Occiput predominantly orange to yellow with darker occipital triangle ..................................................... 2 + + +-. Occiput predominantly brownish black to black ......................................................................................... 3 + + + + + +2. Mesonotum with three distinct dark stripes; antennal flagellomeres brownish black +.... + +formosana +(Okada) + + + + + +-. Mesonotum with three stripes, median stripe orange and two admedian stripes black ( +Fig. 1 +); antennal flagellomeres yellowish orange + +............................................................... +sinica + +Xu, Cao et Evenhuis, + +n. sp. + + + + + + + +3. Veins M2 and CuA1 reaching wing margin ( +Fig. 6 +); only tergites IV–V orange .......................................... + +............................................................................................................ +completa + +Xu, Cao et Evenhuis, + +n. sp. + + + + +-. Veins M2 and CuA1 not reaching wing margin; tergites IV–V not as above.............................................. 4 + + + + +4. Abdomen predominantly black with some paler markings ......................................................................... 5 + + + +-. Abdomen with more uniform coloration, either black or brownish yellow; gonostyli with two large teeth +......................................................................................................................................... + +semirufa +(Meigen) + + + + + + + +5. Gonostyli reduced, apex with only one dark tooth ( +Fig. 11 +); paramere strong, in lateral view ( +Fig. 12 +) shaped like a broom, with very dense black short hairs apically + +.......... +singula + +Xu, Cao et Evenhuis, + +n. sp. + + + + + +-. Gonostyli normal in size, with two dark teeth apically ( +Fig. 13 +), two minute dark sclerotized teeth in between large darkly sclerotized ones + +.......................................... +wolongensis + +Xu, Cao et Evenhuis, + +n. sp. + + + + + + + \ No newline at end of file diff --git a/data/38/02/59/3802590CFE16643029C1F947FDEEEDDC.xml b/data/38/02/59/3802590CFE16643029C1F947FDEEEDDC.xml new file mode 100644 index 00000000000..e4a62e15184 --- /dev/null +++ b/data/38/02/59/3802590CFE16643029C1F947FDEEEDDC.xml @@ -0,0 +1,168 @@ + + + +Four new species of Isoneuromyia from China (Diptera: Keroplatidae) + + + +Author + +Xu, Huachao + + + +Author + +Cao, Jian + + + +Author + +Wu, Hong + + + +Author + +Evenhuis, Neal L. + + + +Author + +Zhou, Zuji + +text + + +Zootaxa + + +2007 + +1423 + + +51 +57 + + + +journal article +10.5281/zenodo.175701 +e41d47ba-2b34-4952-a9a5-08731dd08567 +1175-5326 +175701 + + + + + + + +Isoneuromyia completa +Xu, Cao et Evenhuis + +, +n. sp. + + + + +( +Figs. 2, 6 +, +10 +) + + + + +Diagnosis. +Closest to + +I. semirufa + +but can be distinguished from it by having only tergites IV–V orange (these tergites not contrasted in colour in + +semirufa + +), the hind coxa and femur being black (dusky brown in + +semirufa + +) and the gonocoxites bilobed from the middle (bilobed from one-third basally in + +semirufa + +). Apex of gonostyli with two dark black teeth and without minute tooth are also good characters to distinguish it from other Chinese species of the genus. + + + + +Description. +MALE. Lengths: Body: +8.2mm +; wing: +5.7 mm +. + + +Head +. Vertex and occiput black, with fairly dense small black recumbent hairs. Ocelli in horizontal line. Frons light brown, bare. Antennae: scape and pedicel cup-shaped, brownish black. Flagellum: segments slightly compressed, brownish black. Face brown, with small black hairs apicolaterally. Palpi and Proboscis brown. + + +Thorax +. Mesonotum ( +Fig. 2 +) brown or brownish black, with conspicuous bare strips between the double or treble rows of acrostichal and dorsocentral brown bristles. Scutellum brownish black. Patch of thick black setae above wing root and on posterior margin of scutellum. Prescutellar area tapering to scutellum. Pronotal lobes dark brown with dense black setae. Pleura, laterotergite and mediotergite brownish black, bare. Halter yellow, knob yellow with brown dorsally. + + +Legs +. Fore and mid coxae brownish, hind coxa black; fore coxa, and apex of mid and hind coxae, with recumbent black hairs. Fore and mid femora yellow, hind femur black, all with recumbent black hairs. Fore tibia without comb, mid with only posterior comb, hind tibiae with anterior and posterior comb. Tibial spurs black. Fore and mid basitarsus subequal in length to lengths of respective tibiae, hind basitarsus 0.7x length of hind tibia. Claws minute. + + +Wing +( +Fig. 6 +). Hyaline, with brown infuscation subapically from costa to middle of cell m2, fading posteriorly; apex of cell cup and cell a1 with light brown cloud apically; vein R4 slightly sinuous, ending in C slightly beyond end of R1; veins M2, CuA1 and A1 reaching wing margin. + + +Abdomen +. Tergites I–III brownish black, tergites IV–V orange, tergites VI–VIII brownish black, all tergites with dense recumbent black hairs. Sternites patterned as on tergites. + + +Hypopygium +( +Fig. 10 +). Not dissected. Gonocoxites brownish black, black pilose on about apical half. Gonostyli brownish black, densely black pilose, apex with two dark black teeth. + +FEMALE. Unknown. + + +Types +. + +Holotype +ɗ (ZJFC +060219 +) and +paratype +ɗ from: Sichuan province: Wanglang National Natural Reserve, +2500 m +, +25 July 2006 +, Jian Cao. + + + + +Etymology. +The species epithet derives from the Latin +completus += complete, referring to veins M2, CuA1 and A1 reaching wing margin. + + + + \ No newline at end of file diff --git a/data/38/02/59/3802590CFE17643629C1FAE3FE24EA9C.xml b/data/38/02/59/3802590CFE17643629C1FAE3FE24EA9C.xml new file mode 100644 index 00000000000..11ceec9e862 --- /dev/null +++ b/data/38/02/59/3802590CFE17643629C1FAE3FE24EA9C.xml @@ -0,0 +1,222 @@ + + + +Four new species of Isoneuromyia from China (Diptera: Keroplatidae) + + + +Author + +Xu, Huachao + + + +Author + +Cao, Jian + + + +Author + +Wu, Hong + + + +Author + +Evenhuis, Neal L. + + + +Author + +Zhou, Zuji + +text + + +Zootaxa + + +2007 + +1423 + + +51 +57 + + + +journal article +10.5281/zenodo.175701 +e41d47ba-2b34-4952-a9a5-08731dd08567 +1175-5326 +175701 + + + + + + + +Isoneuromyia singula +Xu, Cao et Evenhuis + +, +n. sp. + + + + +( +Figs. 3, 7 +, +11, 12 +) + + + + +Diagnosis. +Similar to + +I. yorki +Evenhuis + +in both having the vertex and occiput black and the tibial spurs black. It can be easily distinguished from + +I. yorki + +by gonostyli reduced, with only one dark tooth and paramere strong, in lateral view shaped like a broom, with very dense black short hairs apically (paramere relatively weak and gonostyli subtriangular in shape, apex with two black teeth apically in + +yorki + +). + + + + +Description. +MALE. Lengths: Body: +7.2 mm +; wing: +5.6mm +. + + +Head +. Vertex and occiput black, with fairly dense small black recumbent hairs. Ocelli in horizontal line. Frons light brown, bare. Antennae: scape and pedicel cup-shaped, brownish black. Flagellum: segments slightly compressed, brownish black. Face brown, with small black hairs apicolaterally. Palpi brown. Proboscis yellowish brown. + + +Thorax +. Mesonotum ( +Fig. 3 +) brownish black, with brown bristles. Scutellum black. Patch of thick black setae above wing root and on posterior margin of scutellum. Prescutellar area tapering to scutellum. Pronotal lobes black with dense black setae. Pleura, laterotergite and mediotergite brownish black, bare. Halter light brown, knob ivory white dorsally. + + + +FIGURES 9–13. + +Isoneuromyia + +male genitalia. 9. + +I. sinica + +, + +n. sp. + +ventral view (cerci and proctiger omitted). 10. + +I. completa + +, + +n. sp. + +ventral view (cerci and proctiger omitted). 11. + +I. singula + +, + +n. sp. + +ventral view (cerci and proctiger omitted). 12. + +I. singula + +, + +n. sp. + +lateral view (gonostyli omitted) 13. + +I. wolongensis + +, + +n. sp. + +ventral view (cerci and proctiger omitted). Scale bar = 0.1 mm. + + + +Legs +. Coxae yellow with brown basally, fore coxa, and apex of mid and hind coxae, with recumbent black hairs. Fore and mid femora brownish black at base, remainder of them ivory white; hind femur black, all with recumbent black hairs. Fore tibia without comb, mid with only posterior comb, hind tibiae with anterior and posterior comb. Tibial spurs black. Fore basitarsus 1.3x length of fore tibia, mid basitarsus subequal in length to length of mid tibiae, hind basitarsus 0.8x length of hind tibia. Claws minute. + + +Wing +( +Fig. 7 +). Hyaline, with brown infuscation subapically from costa to middle of cell m2, fading posteriorly; vein R4 straight, ending in C slightly beyond end of R1; vein M2, CuA1 not reaching wing margin, A1 quite reaching wing margin. + + +Abdomen +. tergites I–II black; tergite III brownish black with white spots at basal sides; tergites IV sometimes with smaller white spots basolaterally; tergites V–VIII brownish black, all of the tergites with dense recumbent black hairs. Sternites patterned as on tergites. + + +Hypopygium +( +Figs. 11, 12 +). Not dissected. Gonocoxites brownish, with black pilose on about apical half. Gonostyli reduced, brown, with black pilose, apex with only one dark tooth. Paramere strong, in lateral view shaped like a broom, with very dense black short hairs apically. + + +FEMALE. +As +in male, but terminal segments of abdomen (III–V) expanded; cerci brown, small, only slightly exserted. + + + +Types +. + +Holotype +ɗ (ZJFC +060222 +) and +paratype +from: +China +: Sichuan province: Wanglang National Natural Reserve, +2500 m +, +26 July 2006 +, Jian Cao, Yiping Wang +et al +. + + + + +Etymology. +The species epithet derives from the Latin +singulus += single, referring to the gonostylar apex with only one tooth. + + + + \ No newline at end of file diff --git a/data/38/02/AB/3802ABB942B55495F64AA9B77FF0627D.xml b/data/38/02/AB/3802ABB942B55495F64AA9B77FF0627D.xml new file mode 100644 index 00000000000..66b3e176555 --- /dev/null +++ b/data/38/02/AB/3802ABB942B55495F64AA9B77FF0627D.xml @@ -0,0 +1,164 @@ + + + +New records of ant species from Yunnan, China + + + +Author + +Liu, Cong + + + +Author + +Guenard, Benoit + + + +Author + +Garcia, Francisco Hita + + + +Author + +Yamane, Seiki + + + +Author + +Blanchard, Benjamin + + + +Author + +Yang, Da-Rong + + + +Author + +Economo, Evan + +text + + +ZooKeys + + +2015 + +477 + + +17 +78 + + + + +http://dx.doi.org/10.3897/zookeys.477.8775 + +journal article +http://dx.doi.org/10.3897/zookeys.477.8775 +1313-2970-477-17 +DFE4A6FC77284576A1F4BD1D38173811 +DFE4A6FC77284576A1F4BD1D38173811 + + + +Taxon classification Animalia Hymenoptera Formicidae + + + +Aenictus paradentatus Jaitrong, Yamane & Tasen, 2012 +Figure 4 + + + +Material examined. + + +CHINA +, +Yunnan +, +Xishuangbanna +: +XTBG +( +21.911°N +, +101.281°E +), Limestone forest, + +06.vi.2013 + +, +46 workers +, + +655m + +, +Hand collection +, + +B. +Guenard + +, +B. Blanchard +and +C. Liu + +. + + + + +Distribution +. + + +Yunnan (new record), Vietnam, Laos, and Thailand (Figure 4 +C +). This collection represents the northern-most record of +Aenictus paradentatus +. + + + +Figure 4. +Aenictus paradentatus +worker, CASENT0716195. A Head in front view B Mesosoma in profile view C Global distribution map. + + + + +Taxonomic note. + +Aenictus paradentatus +is very similar to +Aenictus dentatus +Forel, 1911, and can be easily identified with the key of +Jaitrong et al. (2012) +. + + + +Natural history. + +Aenictus paradentatus +has been collected from foraging columns on the ground in limestone forest, but was also reported to be found in other forest habitats, ranging from primary forest to disturbed forest ( +Jaitrong et al. 2012 +). + + + + \ No newline at end of file diff --git a/data/38/02/D6/3802D6EFCAEA6C8307329BC7A396475D.xml b/data/38/02/D6/3802D6EFCAEA6C8307329BC7A396475D.xml new file mode 100644 index 00000000000..35d256e928a --- /dev/null +++ b/data/38/02/D6/3802D6EFCAEA6C8307329BC7A396475D.xml @@ -0,0 +1,235 @@ + + + +Studies of Malagasy Eugenia - IV: Seventeen new endemic species, a new combination, and three lectotypifications; with comments on distribution, ecological and evolutionary patterns + + + +Author + +Snow, Neil +T. M. Sperry Herbarium, Department of Biology, Pittsburg State University, 1701 S. Broadway, Pittsburg, KS 66762 USA +nsnow@pittstate.edu + + + +Author + +Callmander, Martin +Missouri Botanical Garden, P. O. Box 299, St. Louis, MO 63166 - 0299, USA & Conservatoire et Jardin botaniques de la Ville de Geneve, case postale 60, 1292 Chambesy, Switzerland + + + +Author + +Phillipson, Peter B. +Missouri Botanical Garden, P. O. Box 299, St. Louis, MO 63166 - 0299, USA & Institut de systematique, evolution, et biodiversite (ISYEB), Unite mixte de recherche 7205, Centre national de la recherche scientifique / Museum national d'Histoire Naturelle / Ecole pratique des hautes etudes, Universite Pierre et Marie Curie, Sorbonne Universites, CP 39, 57 rue Cuvier, F- 75231 Paris cedex 05, France + +text + + +PhytoKeys + + +2015 + +2015-04-28 + + +49 + + +59 +121 + + + + +http://dx.doi.org/10.3897/phytokeys.49.9003 + +journal article +http://dx.doi.org/10.3897/phytokeys.49.9003 +1314-2003-49-59 +FF802B61FFBB3565FF8C33265003FF97 +576302 + + + + +Eugenia barriei N. Snow +sp. nov. +holotype: (Figure 3): http://www.tropicos.org/Image/100314913 + + + + + +Haec +species a congeneris madagascariensibus pedicellis gracilibus delicatis, foliis tenuiter coriaceis, floribus minutis atque hypanthio dense villoso distinguitur. + + + + +Type. + +Madagascar. Prov. Mahajanga: Fiv. Port +Berge +, Marosely, Bongolava, +15°38'58"S +, +47°35'03"E +, 217 m, 17 Nov. 2004, R. Razakamalala 1735 + R. Ramananjanahary & A. Rabezafy (holotype: MO-4849778!). + + + +Description. + +Shrubs to 3 m tall; bark of main bole unknown. Vegetative and reproductive parts (where indicated) bearing a moderately dense, shortish indumentum, the individual trichomes dibrachiate or not, appressed to somewhat reflexed (appearing villous), frequently irregularly contorted, whitish or reddish. Branchlets laterally compressed but becoming rounded, smooth, moderately short villous (hairs mostly reflexed and not dibrachiate) becoming glabrous, oil glands common and prominent (after indumentum falls away). Leaves opposite, mostly occurring in 2-4 pairs along seasonal growth of branchlet, thinly coriaceous, venation brochidodromous (invisible to obscure), discolorous, somewhat glossy above but matte below. Axillary colleters +absent +. Petioles 1.7-2.5 mm long, broadly sulcate above, moderately hairy towards base adaxially in sulcus. Leaf blades 0.9-2.0 (-2.7) +x +0.6-0.9 cm, narrowly elliptic or elliptic to narrowly obovate, base cuneate, surface flat to slightly and irregularly (but broadly) sinuous on drying, margin flat or drying slightly revolute, apex obtuse; abaxial surface glabrescent, oil glands common (use magnification) and drying brownish and slightly sunken, midvein flush and becoming imperceptible towards apex; abaxial surface sparsely glabrescent, oil glands relatively sparse to moderate and somewhat less prominent than adaxially, secondary veins few and barely perceptible, the secondaries connected at their ends by a slightly arching pseudo-intramarginal vein 0.3-0.8 mm from leaf margin (i.e., lacking an intramarginal vein distinct from pseudo-intramarginal vein). Inflorescence a monad; the base of the flowering branchlets each with (2-)4-6 flowers arising alternately, each flower subtended by a short, hairy and somewhat ovate to broadly triangular caducous bract. Pedicels (5-)10-15(-20) mm long, 0.3-0.5 mm wide, round in transverse section, stiff, ascending, sparsely hairy (especially near base) to nearly glabrous, moderately glandular throughout, anthopodium present or absent. Bracteoles 2, linear, 1.0-1.2 +x +0.3-0.5 mm, sparsely hairy. Hypanthium cupulate 2.0-2.5 mm long, 1.4-1.8 mm wide at base of calyx lobes, densely short-hairy, oil glands absent or sparse (and obscured by hairs); ovary apex glabrous. Calyx lobes 4, 1.5-1.9 mm, broadly ovate to rounded, glabrous on both faces apart from sparse apical hairs (white or reddish), strongly reflexed in athesis. Petals 4 (material scant), ca. 2.5 mm +x +2 mm, obovate to widely obovate, glabrous on both faces apart from sparse apical hairs (contorted irregularly), oil glands absent. Staminal region (i.e., lacking a well-defined staminal ring) 1.6-1.8 mm diameter in anthesis, sparsely hairy (trichomes simple); stamens 35-45; filaments 1.5-2.5 mm; anther sacs 0.5-0.7 mm long, globose, basifixed, eglandular. Style 2.5-2.8 mm, glabrous or sparsely hairy basally; stigma narrow and only slightly capitate. Fruit unknown. + + + +Figure 3. +Holotype specimen of + +Eugenia barriei + +(MO). + + + + +Etymology. + +The specific epithet honors Dr. Fred Barrie (b. 1948) of the Missouri Botanical Garden in recognition of his contributions to our knowledge of + +Eugenia + +and other genera of Mesoamerican +Myrtaceae +(e.g., +Barrie 2004 +, +2005 +). + + + +Phenology. +Flowering confirmed only for the middle of November; fruiting likely late November through December. + + +Distribution. + +Known only from near Port +Berge +in Mahajanga Province (Figure +4 +). + + + +Figure 4. +Distribution of new + +Eugenia + +species in Madagascar with selected Protected Areas (hatched): + +Eugenia barriei + +(star), + +Eugenia delicatissima + +(squares), + +Eugenia malcomberi + +(triangle), + +Eugenia ranomafana + +(circles), and + +Eugenia ravelonarivoi + +(crosses). + + + + +Conservation status. + +With only one collection known from Central-western Madagascar collected in an unprotected and threathened dry forest, + +Eugenia barriei + +is assigned a preliminary risk of extinction of "Critically Endangered" [CR A3c] following the IUCN Red List Categories and Criteria ( +IUCN 2012 +). In the absence of effective protection and the high human pressure on these forests, it is unlikely that the forest will persist beyond 3 generations of + +Eugenia barriei + +(ca. 30 years). + + + +Comments. + +The type specimen of + +Eugenia barriei + +initially was determined as + +Eugenia tropophylla + +H. Perrier. The latter species and the varieties described by + +Perrier de la +Bathie +(1953a + +, +b +) do not represent a single taxon, which even a cursory glance at the numerous syntypes (at P) will reveal. + + +Among +taxa from southeastern Africa, + +Eugenia barriei + +resembles some specimens of +Eugenia capensis subsp. gracilipes +. In particular, the slender pedicels of a specimen from Malawi (Chapman 6570 [MO]) have a similar but less dense indumentum on the branchlets, pedicels and hypanthium. Other differences of the Chapman specimen include longer and more densely and prominently punctate leaves, and inflorescences that mostly arise from ramiflorous brachyblasts. + + + +Eugenia barriei + +also has gross morphological similarity to the widespread and relatively common west African species + +Eugenia leonensis + +Engler & Brehmer (e.g., D.K. Harder 3372 et al. [MO] from Ghana), but it differs from that species by the generally glabrous aspect of the latter. Likewise, + +Eugenia barriei + +somewhat resembles + +Eugenia mufindiensis + +Verdc. by virtue of the indumentum of the branchlets, but the latter differs by its much more densely punctate leaves (above and below), the glabrous hypanthium, and a narrower and more deeply sulcate petiole (e.g., M.A. Mwangoka 5945 + H. Mgalla [MO]). + + + + \ No newline at end of file diff --git a/data/38/03/60/38036061F63AEFD7F618DF95317E0D6C.xml b/data/38/03/60/38036061F63AEFD7F618DF95317E0D6C.xml new file mode 100644 index 00000000000..f216b46715d --- /dev/null +++ b/data/38/03/60/38036061F63AEFD7F618DF95317E0D6C.xml @@ -0,0 +1,104 @@ + + + +Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea + + + +Author + +Dale-Skey, Natalie + + + +Author + +Askew, Richard R. + + + +Author + +Noyes, John S. + + + +Author + +Livermore, Laurence + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8013 +8013 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8013 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8013 +1314-2828--8013 + + + + +Encarsia inaron (Walker, 1839) + + + + +Aphelinus inaron +Walker, 1839 + + +idaeus +(Walker, 1839, +Aphelinus +) + + +borealis +Hulden, 1986 + + +brassicae +Shafee & Bela, 1984 + + +indifferentis +Mercet, 1929 + + +partenopea +Masi, 1909 + + +aleyrodis +(Mercet, 1930, +Trichaporus +) + + + +Distribution +England + + + \ No newline at end of file diff --git a/data/38/03/63/3803633FE03B5577ADB2739999D2ED9B.xml b/data/38/03/63/3803633FE03B5577ADB2739999D2ED9B.xml new file mode 100644 index 00000000000..0dddf294f91 --- /dev/null +++ b/data/38/03/63/3803633FE03B5577ADB2739999D2ED9B.xml @@ -0,0 +1,105 @@ + + + +A revision of the genus Psammogorgia Verrill, 1868 (Cnidaria, Anthozoa, Octocorallia) in the tropical eastern Pacific Ocean + + + +Author + +Breedy, Odalisca +Centro de Investigacion en Estructuras Microscopicas, Centro de Investigacion en Ciencias del Mar y Limnologia, Escuela de Biologia, Universidad de Costa Rica. P. O. Box 11501 - 2060, Universidad de Costa Rica, San Jose, Costa Rica & Smithsonian Tropical Research Institute, P. O. Box 0843 - 03092, Panama, Republic of Panama +odaliscab@gmail.com + + + +Author + +Guzman, Hector M. +Smithsonian Tropical Research Institute, P. O. Box 0843 - 03092, Panama, Republic of Panama + +text + + +ZooKeys + + +2020 + +961 + + +1 +30 + + + + +http://dx.doi.org/10.3897/zookeys.961.54846 + +journal article +http://dx.doi.org/10.3897/zookeys.961.54846 +1313-2970-961-1 +C5E8BED7F08549A999C60C3AA8492D09 +634A9CDA65075FEE8D7C196F5E37F6FC + + + + +Psammogorgia hookeri Breedy & Guzman, 2014 +Figure 14 + + + + +Psammogorgia hookeri +Breedy & Guzman, 2014: 2-5. + + + +Type locality. + +Isla +Gallan +, Paracas National Reserve, +Peru +. + + + +Diagnosis. + +Colonies coral red, small, bushy, multiplanar and irregularly dichotomous. Coenenchyme granular. Coenenchymal sclerites: wide, irregular spindles with acute or bifurcated ends, and combinations of both; warty and irregular radiates, crosses and conspicuous star-like radiates. Colours of coenenchymal sclerites reddish, coral red, and lighter. Calyces prominent, swollen and closely placed. Thorny, irregular spindles, and wart-clubs around the calyx rim up to 0.16 mm long. Anthocodial spindles, thin and spiny, in collaret and points arrangements, yellowish, and pale pink in colour. We refer to +Breedy and Guzman (2014) +for a full description of the species. + + + +Distribution. + +This species has only been reported for +Peru +, Isla +Gallan +, Paracas National Reserve at 25 m depth, and from +Bahia +Independencia at unknown depth (Fig. +14 +). + + + +Figure 14. + +Psammogorgia hookeri + +Breedy & Guzman, 2014. +In situ +colonies at Isla San +Gallan +, Paracas National Reserve, 25 m deep. Photograph: Yuri Hooker (UPCH). + + + + + \ No newline at end of file diff --git a/data/38/03/66/38036608245B3BDD769353D8ADA6D198.xml b/data/38/03/66/38036608245B3BDD769353D8ADA6D198.xml new file mode 100644 index 00000000000..e52c7b7880f --- /dev/null +++ b/data/38/03/66/38036608245B3BDD769353D8ADA6D198.xml @@ -0,0 +1,80 @@ + + + +Hornmilben (Oribatida) [pages 69 to 101] + + + +Author + +Weigmann, G. + + + +Author + +Miko, L. + +text + + +2006 +Goecke & Evers + +Keltern + + + +Hornmilben (Oribatida) [Dahl, Tierwelt Deutschlands, Teil 76] + + + +69 +101 + + + + +http://www.goeckeevers.de/verlag/dahl.html + +book chapter +Weigmann2006pp69to101 + + + + +Haplochthoniidae +van der Hammen, 1959 + + + + +Diagnose: +Weiss +, kaum sklerotisiert; Borsten +duenn +bis lanzettlich und glatt; NG mit 16 ng, in vier Platten unterteilt: Na, Nm1, Nm2, Py; Na mit c1-c3 und d3; Nm1 mit d1 und d2; Nm2 mit e1 und e2; Py mit f1, f2, h1-h3, p1-p3; in +Laengsreihe +bei c1 bis h1 je ein "Porenpaar"; ohne PA und AG; Epi-Formel 3-2-2-4 ( +Haplochthonius +) oder 3-2-2-3 ( +Amnemochthonius +); B 1-krallig. + + + + +In Mitteleuropa nur eine Gattung und Art: [ +Haplochthonius simplex +(Willmann, 1930)] + + +(in +Suedeuropa +und Afrika auch +H. sanctaeluciae +Bernini, 1973). + + + + \ No newline at end of file diff --git a/data/38/03/87/380387B5EF28DC4FFEA2FB97FEB8FD6E.xml b/data/38/03/87/380387B5EF28DC4FFEA2FB97FEB8FD6E.xml new file mode 100644 index 00000000000..e633a052fbf --- /dev/null +++ b/data/38/03/87/380387B5EF28DC4FFEA2FB97FEB8FD6E.xml @@ -0,0 +1,240 @@ + + + +Description of ® ve new species of Exogoninae Rioja, 1925 (Polychaeta: Syllidae) associated with the stony coral Mussismilia hispida (Verrill, 1868) in SaÄo Paulo State, Brazil + + + +Author + +Nogueira, J. M. De M. + +text + + +Journal of Natural History + + +2001 + +35 + + +1773 +1794 + + + +journal article +1464-5262 + + + + + + +Grubeosyllis longiarticulata + +n. sp. + + +(®gure 5) + + + +Material examined + + + +Holotype +and +paratype +1 from +Ilha dos Alcatrazes +and +paratypes +2± 5 from + +Laje +de Santos + + +. +Holotype +(MHN-BPO 68-0): complete specimen, +1.9 mm +long, +0.13 mm +wide, with 27 chaetigers. +Paratype +1 (MHN-BPO 68-1): complete specimen, +1 mm +in length, +0.14 mm +wide, with 15 chaetigers; +paratype +2 (MHN-BPO 68-2): incomplete specimen, +0.18 mm +wide, with 24 chaetigers; +paratype +3 (MHN-BPO 68-3): complete specimen, +1.25 mm +long, +0.15 mm +wide, with 22 chaetigers; +paratype +4 (MHN-BPO 68-4): complete specimen, +2 mm +long, +0.13 mm +wide, with 28 chaetigers; +paratype +5 (MHN-BPO 68-5): complete specimen, +2.47 mm +long, +0.17 mm +wide, with 28 chaetigers. + + +Description + + +Body small, slender, without colour markings. Prostomium rectangular to square, somewhat wider than long, partially covered posteriorly by peristomium; four lensed eyes in open trapezoidal arrangement and two anterior eyespots. Antennae with bulbous base and slender tips; lateral antennae originating on lateral margin of prostomium, between anterior eyes and eyespots, shorter than prostomium and palps together; median antenna inserted between posterior pair of eyes and longer than prostomium and palps together. Palps proportionally short and broad, shorter than prostomium, dorsally connected by a membrane, leaving a distal notch (®gure 5A). Peristomium long, similar in length to following segments, with two pairs of tentacular cirri similar in shape and size to the antennae; dorsal pair longer than ventral pair. Dorsal cirri of chaetiger 1 longer than the following; remaining anterior cirri with bulbous bases and slender tips, becoming more slender and longer progressively, from midbody to the posterior segments; dorsal cirri from chaetigers 2 and 3 short (®gure 5A). Ventral cirri digitiform and shorter than parapodial lobes. Parapodia each with six to eight heterogomph compound chaetae with long, bidentate blades, provided with long, thin spines basally, diminishing progressively in size and number towards tips, becoming smooth distally (®gure 5C, G), distal tooth slender, proximal tooth long, slender, slightly shorter than distal tooth; strong gradation dorsoventrally in size of blades; superior falcigers about + +33±34 +m + +m, midlength blades, + +24±25 +m + +m, and most inferior ones, + +16±18 +m + +m. Antero-posterior gradation not strongly marked, but blades of posterior compound chaetae somewhat shorter and wider than anterior (®gure 5C, G). Solitary dorsal simple chaetae from chaetiger 6 on +holotype +and even more anteriorly in other specimens (from chaetiger 2 on +paratype +1), very thin, unidentate and minutely serrated (®gure 5F); solitary ventral simple chaetae on last chaetiger of +holotype +, somewhat thicker than dorsal, shorter, strongly bidentate, with smooth cutting edges, or provided with very short, straight spines (®gure 5H). Parapodia each with a solitary aciculum provided with a subdistal enlargement and an acuminate tip (®gure 5E), frequently protruding out from parapodia; anterior parapodia each provided with another aciculum, small and nearly straight (®gure 5D). Pygidium small, rectangular to trapezoidal, with one pair of long and slender anal cirri, and one to three papillae (®gure 5B). Pharynx long and narrow, extending through three or four segments, provided with a rhomboidal subterminal tooth. Proventriculum wide, occupying three or four segments, with about 24 rows of muscle cells (®gure 5A). + + + +FIG. 5. + +Grubeosyllis longiarticulata + +, +n. sp. +: (A) anterior part, dorsal view (holotype); (B) posterior part, dorsal view; (C) compound chaetae, anterior parapodium; (D) acicula, anterior parapodium; (E) aciculum, posterior parapodium; (F) dorsal simple chaeta; (G) compound chaetae, posterior parapodium; (H) ventral simple chaeta. Scale bar: (A, B): 0.34 mm; (C±G) 20 +m +m. + + + +Etymology + + +As with the previous species, the name + +longiarticulata + +reēcts the size of the blades of compound chaetae. + + +Discussion + + +Several species of + +Grubeosyllis + +possess bidentate falcigers with marked dorsoventral gradation in size of the blades, but most of them have blades much shorter than those of + +G. longiarticulata + +n. sp. + +Grubeosyllis heterocirra +( +Rioja, 1941 +) + +, for example, has a general body aspect very similar to this new species, but the spines of the blades of the uppermost falcigers are longer, extending for a proportionally longer extension, and, especially, the blades are much shorter (about + +19 +m + +m) (see +Westheide, 1974b +). Other species, such as + +G. clavata +(ClapareÁde, 1863) + +, + +G. limbata +(ClapareÁde, 1868) + +, + +G. rugulosa +Verrill, 1900 + +and + +G. vieitezi + +(San MartõÂn, 1984a) are easily distinguished from + +G. longiarticulata + +n. sp. +by shape and length of the blades of the compound chaetae and by the length of dorsal cirri on chaetiger 1, compared with the following cirri (see San MartõÂn, 1984a, 1991). On the other hand, + +G. euritmica + +( +SardaÂ, 1984 +) also has long chaetal blades, but it is diOEerent from + +G. longiarticulata + +n. sp. +in having: (1) dorsal cirri of chaetiger 1 only slightly longer than those of the following segments; (2) parapodia each with about 12 compound chaetae; (3) strong anteroposterior gradation in size of the blades; (4) large and rounded gap between both teeth of the blades; (5) short spines all along cutting edges of the blades; (6) solitary dorsal simple chaetae bidentate; and (7) proventriculum with about 15±20 rows of muscle cells. + +Grubeosyllis longisetosa + +(Hartmann-SchroÈder, 1979) has long chaetal blades, similar to those of + +G. longiarticulata + +n. sp. +, but diOEers from it in having: (1) much longer dorsal cirri; (2) shorter spines on cutting edges of the blades of the compound chaetae, with proportionally shorter proximal tooth; and (3) pharynx shorter, with pharyngeal tooth located away from the margin, nearly in the middle of the pharynx (see Hartmann-SchroÈder, 1979). + +Grubeosyllis neapolitana +( +Goodrich, 1930 +) + +is diOEerent in having: (1) blades with proximal tooth very small, resembling a spine; (2) acicula distally rounded; (3) solitary ventral simple chaetae unidentate; (4) pharynx with papillae on margin; and (5) pharyngeal tooth located away from margin of the pharynx (see + +JimeÂnez +et al +., 1994 + +). Finally, + +G. nitidula +Verrill, 1900 + +, diOEers because: (1) median antenna originates between anterior pair of eyes; (2) blades of the compound chaetae of anterior chaetigers are only slightly bidentate, with both teeth very close; (3) blades of compound chaetae of posterior chaetigers with short spines; (4) solitary dorsal simple chaetae bidentate; (5) pharynx and proventriculum shorter; and (6) proventriculum with only 16 rows of muscle cells. + + + + \ No newline at end of file diff --git a/data/38/03/87/380387B5EF30DC50FE51FFD3FC2FFA90.xml b/data/38/03/87/380387B5EF30DC50FE51FFD3FC2FFA90.xml new file mode 100644 index 00000000000..f4752240f69 --- /dev/null +++ b/data/38/03/87/380387B5EF30DC50FE51FFD3FC2FFA90.xml @@ -0,0 +1,329 @@ + + + +Description of ® ve new species of Exogoninae Rioja, 1925 (Polychaeta: Syllidae) associated with the stony coral Mussismilia hispida (Verrill, 1868) in SaÄo Paulo State, Brazil + + + +Author + +Nogueira, J. M. De M. + +text + + +Journal of Natural History + + +2001 + +35 + + +1773 +1794 + + + +journal article +1464-5262 + + + + + + +Sphaerosyllis brasiliensis + +n. sp. + + +(®gure 2) + + + +Material examined + + + +Holotype +from +Ilha dos Alcatrazes +, +three paratypes +from + +Laje +de Santos + + +. +Holotype +(MHN-BPO 69-0): complete specimen, +1.1 mm +long, +0.16 mm +wide, with 15 chaetigers. +Paratype +1 (MHN-BPO 69-1): complete specimen, +1.7 mm +long, +0.17 mm +wide, with 20 chaetigers; +paratype +2 (MHN-BPO 69-2): complete specimen, +1.4 mm +long, +0.19 mm +wide, with 15 chaetigers; +paratype +3 (MHN-BPO 69-3): incomplete specimen, with 11 chaetigers, +0.23 mm +wide. + + + +FIG. 2. + +Sphaerosyllis brasiliensis + +, +n. sp. +: (A) anterior part, dorsal view (holotype); (B) posterior part, dorsal view (holotype); (C) compound chaetae, anterior parapodium; (D) acicula, anterior parapodium; (E) dorsal simple chaeta; (F) compound chaetae, posterior parapodium; (G) ventral simple chaeta; (H) aciculum, posterior parapodium. Scale bar: (A, B) 0.55 mm; (C±H) 20 +m +m. + + + +Description + + +Body small, short, without colour markings; dorsal and ventral surfaces of body covered by numerous papillae, often hidden by agglutinated debris. Prostomium ovate, partially covered posteriorly by peristomium; four lensed eyes in trapezoidal arrangement. Antennae small with spherical bases and slender, ®liform tips; lateral antennae inserted in front of anterior eyes, median antenna originating between posterior pair of eyes. Palps short, wider than long, fused along their length, leaving a terminal notch, similar in length to prostomium (®gure 2A). Peristomium similar in length to following segments; tentacular cirri small, similar to antennae. Dorsal cirri small, similar to antennae and tentacular cirri, absent on chaetiger 2, becoming somewhat longer on posterior segments (®gure 2A, B). Parapodia conical, provided with several papillae and bearing ®ve to six compound heterogomph chaetae; blades unidentate; in anterior parapodia, blades of compound chaetae with long, very slender spines on the bases of cutting edges (®gure 2C); in posterior parapodia, blades of compound chaetae smooth (®gure 2F); with strong dorsoventral gradation in size, not so marked anteroposteriorly. In anterior parapodia, blades of uppermost chaetae about + +22.5 +m + +m long, intermediate, + +16 +m + +m, and lower, + +12 +m + +m (®gure 2C); in midbody parapodia, upper, + +22 +m + +m long, intermediate, + +14 +m + +m, and lower, + +11 +m + +m; in each posterior parapodia, upper chaetae + +20 +m + +m long, median, + +12.5 +m + +m, and lower, + +9.5 +m + +m (®gure 2F). Solitary dorsal simple chaetae, from chaetiger 1 on +holotype +, thin, provided with very small spines (®gure 2E); solitary ventral chaetae, on posteriormost parapodia, unidentate, with curved tip, thick and smooth (®gure 2G). Anterior parapodia each with two acicula, one thick, strongly bent at right angle near tip and the other very thin and di cult to see, slightly curved, and with an acuminate tip directed upwards (®gure 2D); each parapodium from midbody with only a solitary strongly bent aciculum (®gure 2H). Pygidium short, semicircular, provided with several papillae and a pair of anal cirri, longer and more elongate than dorsal cirri (®gure 1B). Pharynx extending through about four segments, with a long, triangular tooth located anteriorly; a pair of large pharyngeal glands located at level of chaetiger 1, present in all examined specimens, although sometimes di cult to see. Proventriculum small, short, through about 1.5±2.5 chaetigers, with about 20 rows of muscle cells (®gure 2A). + + +Etymology +This species was named + +brasiliensis + +because the +type +locality is in +Brazil +. + + +Discussion + + +Several species of the genus + +Sphaerosyllis + +have a combination of the following characters: densely papillated body, two pairs of eyes, dorsal cirri and antennae small and clavate, and an absence of both: dorsal cirri on second chaetiger and of parapodial glands; however, none of them has such a strong dorsoventral gradation in the size of the blades of the compound chaetae all over the body, as is seen in + +S. brasiliensis + +n. sp. +The species most similar to + +S. brasiliensis + +n. sp. +are: + +S. californiensis +Hartman, 1966 + +, + +S. austriaca +Banse, 1959 + +, + +S. dubiosa + +Hartmann-SchroÈder, 1962, + +S. pirifera +ClapareÁde, 1868 + +, + +S. asiatica +Buzhinskaja, 1980 + +and + +S. piriferopsis +Perkins, 1980 + +. In this discussion we do not consider diOEerences such as degree of fusion between prostomium and tentacular segment, and slight diOEerences in pharynx length and number of muscle cell rows of the proventriculum, because we agree with +Riser (1991) +that these characters depend mostly on how the animals were preserved. + +Sphaerosyllis californiensis + +diOEers from + +S. brasiliensis + +n. sp. +in having: (1) dorsal cirri on chaetiger 2; (2) somewhat longer palps; (3) papillae on the margin of pharynx; (4) proventriculum with only 13±14 rows of muscle cells, against +20 in + +S. brasiliensis + +n. sp. +; (5) compound chaetae with shorter and proportionally broader blades, especially those of the posteriormost part of the body, with almost no dorsoventral gradation in size, and much more curved; (6) blades of anterior compound chaetae with longer spines along most of the length; and (7) anal cirri similar to dorsal cirri (see +Kudenov and Harris, 1995 +). + +Sphaerosyllis austriaca + +is distinguished from + +S. brasiliensis + +n. sp. +because it has: (1) all three antennae originating on the anterior border of the prostomium; (2) posterior dorsal cirri digitate, with slight diOEerence in thickness between base and tip, and dark pigmented bases; (3) proventriculum with 15 rows of muscle cells; (4) blades of compound chaetae longer (35± + +10 +m + +m, on anterior segments, against 22.5± + +12 +m + +m in + +S. brasiliensis + +n. sp. +), with a subterminal spine; and (5) posterior compound chaetae without dorsoventral gradation (see San MartõÂn, 1984a). + +Sphaerosyllis dubiosa + +diOEers from + +S. brasiliensis + +n. sp. +because it has: (1) longer antennae; (2) four yellow transversal rows per segment; and (3) diOEerent morphology of blades of compound chaetae (see Hartmann-SchroÈder, 1962). + +Sphaerosylli s +pirifera + +is diOEerent because it has: (1) body longer and more robust; (2) antennae, tentacular and dorsal cirri more elongate; (3) posterior dorsal cirri with slight diOEerence of thickness between base and tip; (4) proventriculum extending through more chaetigers (2.5±3 chaetigers, against +1.5±2.5 in + +S. brasiliensis + +n. sp. +), but with fewer rows of muscle cells (only 14 rows); (5) blades of anterior compound chaetae longer (35± + +10 +m + +m), with marked subterminal spine; (6) blades of posterior compound chaetae without dorsoventral gradation in length, shorter, stouter and more curved (see San MartõÂn, 1984a). + +Sphaerosyllis asiatica + +has compound chaetae with proportionally shorter blades, provided with longer and coarser spines on the cutting margin (see +Buzhinskaja, 1980 +). + +Sphaerosylli s +piriferopsis + +is probabl y the most similar species, but it is distinguished by: (1) a pharynx without`yellowish glands’ on chaetiger 1, but with glands surrounding it over its entire length; (2) proventriculum with 13±14 rows of muscle cells; (3) solitary aciculum on every parapodium; (4) blades of anterior compound chaetae slightly shorter ( + +17 +m + +m); (5) blades of posterior compound chaetae about + +9.5 +m + +m long, without dorsoventra l gradation, stouter and more strongly hooked than those of + +S. brasiliensis + +n. sp. +, in which length varies from 20 to + +10 +m + +m (see +Perkins, 1980 +). + +Sphaerosyllis hystrix +ClapareÁde, 1863 + +and + +S. taylori +Perkins, 1980 + +are species similar to + +S. brasiliensis + +n. sp. +, but easily distinguished from it because both have conspicuous parapodial glands containing rods (see San MartõÂn, 1984a). + + + + \ No newline at end of file diff --git a/data/38/03/87/380387B5EF36DC4AFEA2FCEBFD8BFBEC.xml b/data/38/03/87/380387B5EF36DC4AFEA2FCEBFD8BFBEC.xml new file mode 100644 index 00000000000..b88d5d64e6a --- /dev/null +++ b/data/38/03/87/380387B5EF36DC4AFEA2FCEBFD8BFBEC.xml @@ -0,0 +1,205 @@ + + + +Description of ® ve new species of Exogoninae Rioja, 1925 (Polychaeta: Syllidae) associated with the stony coral Mussismilia hispida (Verrill, 1868) in SaÄo Paulo State, Brazil + + + +Author + +Nogueira, J. M. De M. + +text + + +Journal of Natural History + + +2001 + +35 + + +1773 +1794 + + + +journal article +1464-5262 + + + + + + +Grubeosyllis breviarticulata + +n. sp. + + +(®gure 4) + + + +Material examined + + + +Holotype +and +three paratypes +from +Ilha dos Alcatrazes + +. +Holotype +(MHN-BPO 67-0): complete specimen in good condition, about +1.63 mm +long, +0.24 mm +wide, with 24 chaetigers. +Paratype +1 (MHN-BPO 67-1): complete specimen, +1.01 mm +long, +0.18 mm +wide, with 19 chaetigers; +paratype +2 (MHN-BPO 67-2): complete specimen, +0.93 mm +long, 0,12 mm wide, with 15 chaetigers; +paratype +3 (MHN-BPO 67-3): complete specimen, +1.9 mm +long, +0.2 mm +wide, with 26 chaetigers. + + +Description + + +Body small, slender, without colour markings. Prostomium oval to rectangular, wider than long, not covered by peristomium (®gure 4A). Four small, lensed eyes in trapezoidal arrangement; anterior pair larger than the posterior pair; two anterior ocular eyespots. Antennae long, with broad bases and acuminate tips; lateral antennae originating between anterior eyes and eyespots, slightly shorter than prostomium and palps together; median antenna originating between posterior pair of eyes, similar in length to prostomium and palps together. Palps long, more than twice the length of the prostomium, broad at their bases, triangular, separated in the distal half and fused in the basal half by a dorsal membrane. Peristomium dorsally reduced, bearing two pairs of tentacular cirri, similar in shape to antennae; dorsal pair somewhat longer than ventral pair, and similar in length to lateral antennae. Dorsal cirri long and slender; dorsal cirri of chaetiger 1 much longer than those of following chaetigers (®gure 4A). Ventral cirri digitiform. Parapodia each with about four compound chaetae, heterogomph, with very short blades, strongly bidentate and without marked gradation in length neither dorsoventrally nor anterior-posteriorly; on parapodia in anterior part of the body, blades of dorsalmost falcigers about + +11 +m + +m long, median ones + +9.5 +m + +m, and ventralmost + +8 +m + +m; from midbody, this diOEerence in size is even less, all blades around + +10 +m + +m; all along the body, cutting edges of blades bearing short spines (®gure 4B, E). Single dorsal simple chaeta, long, thin, bidentate, provided with small spines on concave side, present from chaetiger 13, in +holotype +, and from chaetiger +6 in +the +paratype +1 (®gure 4D). Solitary ventral simple chaeta seen only on posteriormost three chaetigers of +paratype +1, thinner, smaller and more curved than dorsal simple chaeta, slightly bidentate. Anterior parapodia each with two acicula, one very slender with a subdistal expansion and pointed tip, and the other much slender, straight, with a slightly curved tip (®gure 4C); only the curved aciculum persists in the posterior parapodia (®gure 4F), thicker than those of the anterior parapodia. Pygidium small with two long and slender anal cirri, and a short, digitate papilla (®gure 4G). Pharynx extending through about four segments, with a long, rhomboidal tooth on anterior margin. Proventriculum wide, through four segments, with about 23 rows of muscle cells (®gure 4A). + + + +FIG. 4. + +Grubeosyllis breviarticulata + +, +n. sp. +: (A) anterior part, dorsal view (holotype); (B) compound chaetae, anterior parapodium; (C) acicula, anterior parapodium; (D) dorsal simple chaeta; (E) compound chaetae, posterior parapodium; (F) aciculum, posterior parapodium; (G) posterior part, lateral view (holotype). Scale bar: (A, G) 0.28 mm; (B±F) 20 +m +m. + + + +Etymology + + +The name + +breviarticulata + +refers to the small size of the blades of the compound chaetae. + + +Discussion + + +The most characteristic features of + +Grubeosyllis breviarticulata + +n. sp. +are long dorsal cirri and short-bladed falcigers. Only few species of this genus share similar characteristics. + +Grubeosyllis balani + +(Hartmann-SchroÈder, 1960) diOEers because: (1) the median antenna is inserted more anteriorly on the prostomium, between the anterior pair of eyes; (2) the dorsal cirri of chaetiger 1 are about the same size as the following cirri and all of them are shorter and have broader bases; and (3) the blades of the compound chaetae have a larger gap between distal and proximal teeth and are even shorter than those of + +G. breviarticulata + +n. sp. +, about + +4±5.5 +m + +m long on anterior parapodia, and + +3±4 +m + +m on posterior ones (see + +AloÂs +et al +., 1983 + +). + +Grubeosyllis brevipharyngea +( +Banse, 1972 +) + +is easily distinguished from + +G. breviarticulata + +n. sp. +because in this species: (1) the palps are totally fused; (2) the peristomium is not dorsally reduced; (3) the dorsal cirri of chaetiger 1 are similar in length to the following cirri; (4) the acicula are distally blunt; (5) each parapodium has seven to nine compound chaetae; (6) there is a strong gradation in size of the chaetae and only the ventralmost are similar to those of + +G. breviarticulata + +n. sp. +; (7) the dorsal simple chaeta is present from the anterior chaetigers; and (8) the pharynx is shorter, extending only through three chaetigers, against four in + +G. breviarticulata + +n. sp. +Finally, + +Grubeosyllis yraidae + +San MartõÂn, 1984a is separated from + +G. breviarticulata + +n. sp. +because the former species has: (1) the palps almost completely fused; (2) the peristomium not reduced; (3) the acicula with very short tip; (4) the blades of superior falcigers with long spines; (5) the blades of inferior falcigers with the proximal tooth very reduced, resembling a spine; (6) the pharynx shorter, only extending through two or three segments; and (7) the pharyngeal tooth placed away from the anterior margin of the pharynx. + + + + \ No newline at end of file diff --git a/data/38/04/4D/38044D1E32E0D3EF74B13C109670A8E4.xml b/data/38/04/4D/38044D1E32E0D3EF74B13C109670A8E4.xml new file mode 100644 index 00000000000..5bc9aa1e404 --- /dev/null +++ b/data/38/04/4D/38044D1E32E0D3EF74B13C109670A8E4.xml @@ -0,0 +1,62 @@ + + + +Species plantarum: exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas + + + +Author + +Linnaeus, Carolus + +text + +1753 +Laurentius Salvius + +Stockholm + + + +https://doi.org/10.5962/bhl.title.669 + +book +10.5281/zenodo.3931989 +3931989 + + + + +Ornithogalum latifolium +, +spec. nov. + + + +6. Ornithogalum racemo longissimo, foliis lanceolato-ensiformibus. + +Ornithogalum latifolium & maximum. +Bauh. pin. 70. + + +Ornithogalum vel Lilium alexandrinum, floribus albis innummerabilibus. +Swert. floril. 58. + + + + +Habitat in +Arabia +, +AEgypto +. + + + + +Folia +pedalia plus quam duos pollices lata. ♃ + + + + \ No newline at end of file diff --git a/data/38/04/76/3804767721292768D714ECCEBEED43FD.xml b/data/38/04/76/3804767721292768D714ECCEBEED43FD.xml new file mode 100644 index 00000000000..0e029d54a1f --- /dev/null +++ b/data/38/04/76/3804767721292768D714ECCEBEED43FD.xml @@ -0,0 +1,300 @@ + + + +Info Flora Schweiz - Rosaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/rosaceae.html + +url + + + + + +Rubus baruthicus +H. E. Weber + + + + + +Art ISFS: 351960 Checklist: 1039170 +Rosaceae +Rubus +Rubus +corylifolius aggr. +Rubus baruthicus H. E. Weber + + +Zusammenfassung +KEINE ANGABE + + + +Status Nationale +Prioritaet + +: -- + + +Internationale Verantwortung +: -- + + + +Oekologie + + + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + +KEINE ANGABE + + +
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+
+
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F--Lichtzahl L--Salzzeichen--
Reaktionszahl R--Temperaturzahl T--
+Naehrstoffzahl +N +-- +Kontinentalitaetszahl +K +--
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Rubus baruthicus +H. E. Weber + + + + + +Volksname + + + +Deutscher Name: -- Nom +francais +: -- Nome italiano: -- + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Rubus baruthicus H. E. Weber + + +Checklist 2017 + +351960
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Kommentare aus der +Checklist 2017 +Nomenklatur + + +, Taxonomie und Vorhandensein im Bearbeitungsgebiet +gemaess +Atlas Florae Europaea (Kurtto et al. 2007). Checklist + + + + +Status Indigenat +: Indigen + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein Status Rote Liste national + + + + + + +
KEINE ANGABE
+
+ + +Status nationale +Prioritaet +/Verantwortung + + + + + + + + + + + + + + + + + + + + + + + + + +
+ +Nationale +Prioritaet + +--
+Massnahmenbedarf +--
+ +Internationale Verantwortung + +--
+ +Ueberwachung +Bestaende + +--
+ +Schutzstatus + + + + + + +
Kein internationaler, nationaler oder kantonaler Schutz
+
+
+
+
\ No newline at end of file diff --git a/data/38/04/90/380490CE3EB75A2FB941E5FF649DED2F.xml b/data/38/04/90/380490CE3EB75A2FB941E5FF649DED2F.xml new file mode 100644 index 00000000000..acfe6acfaa0 --- /dev/null +++ b/data/38/04/90/380490CE3EB75A2FB941E5FF649DED2F.xml @@ -0,0 +1,188 @@ + + + +Checklist of the suborder Terebrantia (Thysanoptera): generic diversity and species composition in Xishuangbanna, Yunnan Province, China + + + +Author + +Elie, Ntirenganya +https://orcid.org/0000-0002-4603-5693 +Plant Protection College, Yunnan Agricultural University, Kunming, 650201, China & Rwandan Association of Ecologists (ARECO Rwanda), Kigali, Rwanda +elientirenganya@gmail.com + + + +Author + +Yajin, Li +Agronomy and Biotechnology College, Yunnan Agricultural University, Kunming, 650201, China + + + +Author + +Yanlan, Xie +Biotechnology and Engineering College, West Yunnan University, Lincang, 677000, China + + + +Author + +Yanli, Zhou +The Germplasm Bank of Wild Species, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, 650201, China + + + +Author + +Hongrui, Zhang +https://orcid.org/0000-0002-0089-1099 +Plant Protection College, Yunnan Agricultural University, Kunming, 650201, China +hongruizh@126.com + +text + + +Biodiversity Data Journal + + +2021 + +2021-11-24 + + +9 + + +72670 +72670 + + + + +http://dx.doi.org/10.3897/BDJ.9.e72670 + +journal article +http://dx.doi.org/10.3897/BDJ.9.e72670 +1314-2828-9-e72670 +705F74B63C8850A08D6DBA243535218D + + + + +Helionothrips shennongjiaensis Feng, Yang & Zhang, 2007 + + + +Materials + + +Type status: + +Other material +. + +Occurrence +: + +recordedBy: + +X.Y. +L + +; individualID: +2017-x-24 +; individualCount: +13 +; sex: +5 males +, +8 females +; lifeStage: +adults +; occurrenceID: YAU5082020 +Tt +18; + +Taxon +: + +scientificNameAuthorship: +Helionothrips +shennongjiaensis +Feng +, +Yang +& +Zhang +; + +Location +: + +country: +China +; stateProvince: +Yunnan +; municipality: +Xishuangbanna +; locality: + +Mengla +( +Tropical Rain Forest +) + +; decimalLatitude: +21.922967 +; decimalLongitude: +101.184971 +; + +Identification +: + +identifiedBy: + +Xie Yanlan + +; dateIdentified: 2018; identificationReferences: ( +ThripsWiki +2020); + +Event +: + +samplingProtocol: +sweeping and shaking +; eventDate: +24/10/2017 +; + +Record Level +: + +collectionID: thrips; institutionCode: YAU5082020; collectionCode: terebrantia; basisOfRecord: preserved specimen + + + + + +Ecological interactions + + +Feeds on +leaves, collected from wide host plants. + + +Distribution + +Described from Hubai China and distributed from Yunnan, Guangdong and Hainan Provinces ( +Feng et al. 2007 +). + + + + \ No newline at end of file diff --git a/data/38/04/B8/3804B86C9DE4578AD0C900067162E6AF.xml b/data/38/04/B8/3804B86C9DE4578AD0C900067162E6AF.xml new file mode 100644 index 00000000000..442ce18be85 --- /dev/null +++ b/data/38/04/B8/3804B86C9DE4578AD0C900067162E6AF.xml @@ -0,0 +1,74 @@ + + + +Checklist of terrestrial Parasitengona mites in Fennoscandia with new species- and distribution records (Acariformes: Prostigmata) + + + +Author + +Stalstedt, Jeanette + + + +Author + +Laydanowicz, Joanna + + + +Author + +Lehtinen, Pekka T + + + +Author + +Bergsten, Johannes + + + +Author + +Makol, Joanna + +text + + +Biodiversity Data Journal + + +2019 + +7 + + +36094 +36094 + + + + +http://dx.doi.org/10.3897/BDJ.7.e36094 + +journal article +http://dx.doi.org/10.3897/BDJ.7.e36094 +1314-2828-7-e36094 + + + + +Abrolophus nymindegabicus Haitlinger, 2008 [L] + + + +Distribution + +Sweden ( +Haitlinger 2008 +). + + + + \ No newline at end of file diff --git a/data/38/04/D3/3804D3DCE41E5ED99A01DA07311E99FE.xml b/data/38/04/D3/3804D3DCE41E5ED99A01DA07311E99FE.xml new file mode 100644 index 00000000000..5303f8b5ea2 --- /dev/null +++ b/data/38/04/D3/3804D3DCE41E5ED99A01DA07311E99FE.xml @@ -0,0 +1,138 @@ + + + +Italian Dermestidae: notes on some species and an updated checklist (Coleoptera) + + + +Author + +Nardi, Gianluca +MiPAAF, Corpo Forestale dello Stato, Centro Nazionale per lo Studio e la Conservazione della Biodiversita Forestale " Bosco Fontana " di Verona, Sede di Bosco Fontana, Strada Mantova 29, I- 46045 Marmirolo (MN), Italy + + + +Author + +Hava, Jiri +Department of Forest Protection and Entomology, Faculty of Forestry and Wood Sciences, Czech University of Life Sciences, Kamycka 1176, CZ- 165 21, Prague 6 - Suchdol, Czech Republic + +text + + +ZooKeys + + +2013 + +2013-12-06 + + +360 + + +45 +81 + + + + +http://dx.doi.org/10.3897/zookeys.360.6023 + +journal article +http://dx.doi.org/10.3897/zookeys.360.6023 +1313-2970-360-45 +441BB156FF9B58304C3BFFBDFFA1FFBD +578089 + + + + +Anthrenus (Nathrenus) signatus Erichson, 1846 + + + + +Anthrenus (Nathrenus) signatus +Erichson, 1846: + +Hava +and Nardi 2011 + +: 428. + + + +Material examined. +Basilicata: Potenza prov., Pignola, Ris. [= Riserva = Reserve] WWF, L. [= Lago = Lake] Pignola, 700 m, 21.VI.1992, FA, 1 ♂ (JHAC). + + +Chorotype. + +European (cf. + +Hava +and Nardi 2011 + +). + + + + +Italian +distribution. + + +South Tyrol, Venetia, Venezia Giulia, Latium?, Apulia, Basilicata and Sicily (cf. + +Hava +and Nardi 2011 + +). + + + +Remarks. + +This species was recorded in Basilicata region from the Pollino National Park ( +Angelini 1986 +) only; the above specimen comes from a nature reserve, from which a sole congeneric species, + +Anthrenus (Nathrenus) verbasci + +, was known so far ( +Angelini 1996a +, +1998 +, both as + +Anthrenus verbasci + +). + + + +Anthrenus signatus + +ab. +bielawskii +Mroczkowski, 1958 from Bulgaria ( +Mroczkowski 1958 +: 6, +1968 +: 145) was recently ignored ( + +Hava +2007 + +, +2008 +, +2011a +), since according to the +ICZN (1999 +, art. 45.5 and 45.6.2), it is an infrasubspecific and unavailable name. + + + + \ No newline at end of file diff --git a/data/38/04/E5/3804E5D332E363D6671BEC44AE004B3E.xml b/data/38/04/E5/3804E5D332E363D6671BEC44AE004B3E.xml new file mode 100644 index 00000000000..72c2617d48d --- /dev/null +++ b/data/38/04/E5/3804E5D332E363D6671BEC44AE004B3E.xml @@ -0,0 +1,75 @@ + + + +An annotated checklist of the scale insects of Iran (Hemiptera, Sternorrhyncha, Coccoidea) with new records and distribution data + + + +Author + +Moghaddam, Masumeh + +text + + +ZooKeys + + +2013 + +334 + + +1 +92 + + + + +http://dx.doi.org/10.3897/zookeys.334.5818 + +journal article +http://dx.doi.org/10.3897/zookeys.334.5818 +1313-2970-334-1 + + + + +● +Phenacoccus betae Moghaddam + + + + +Phenacoccus betae +Moghaddam, 2010a: 65-67. + + + +Iran localities. +Kermanshah, Markazi. + + +Host plants. + +Amaranthaceae +: +Amaranthus blitoides +, +Beta vulgaris +. + + + +References. + +Ben-Dov et al. (2013) +and +Moghaddam (2010a +, +2013 +). + + + + \ No newline at end of file diff --git a/data/38/04/F9/3804F9C17BA310DBC4EEA109F9261C1A.xml b/data/38/04/F9/3804F9C17BA310DBC4EEA109F9261C1A.xml new file mode 100644 index 00000000000..d36591eea3e --- /dev/null +++ b/data/38/04/F9/3804F9C17BA310DBC4EEA109F9261C1A.xml @@ -0,0 +1,90 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part U) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +906 +910 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Utricularia bifida +Linnaeus + +, + +Species Plantarum +1 + +: 18. 1753 + + +. + + + +"Habitat in China. Osbeck." RCN: 150. + + + + +Lectotype +(Taylor in +Kew Bull., Addit. Ser. +14: 308. 1989): +Osbeck s.n. +, Herb. Linn. No. 34.7 ( +LINN +) + +. + + + + +Current name: + + +Utricularia bifida + +L. + +( +Lentibulariaceae +). + + + + \ No newline at end of file diff --git a/data/38/05/1A/38051A775B6BA4DA337F83BA86A078DA.xml b/data/38/05/1A/38051A775B6BA4DA337F83BA86A078DA.xml new file mode 100644 index 00000000000..d88127ab760 --- /dev/null +++ b/data/38/05/1A/38051A775B6BA4DA337F83BA86A078DA.xml @@ -0,0 +1,60 @@ + + + +Brazilian Trichoptera Checklist II + + + +Author + +Paprocki, Henrique + + + +Author + +Franca, Diogo + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1557 +1557 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1557 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1557 +1314-2828--1557 + + + + +Oxyethira peruviana Harris & Davenport, 1999 + + + +Distribution +Amazonas + + +Notes + +Harris and Davenport 1999 +, +Santos et al. 2009 + + + + \ No newline at end of file diff --git a/data/38/05/21/380521101DA779FCF00D2CFCE8AF1C31.xml b/data/38/05/21/380521101DA779FCF00D2CFCE8AF1C31.xml new file mode 100644 index 00000000000..59c70edabe5 --- /dev/null +++ b/data/38/05/21/380521101DA779FCF00D2CFCE8AF1C31.xml @@ -0,0 +1,86 @@ + + + +A survey of basal insects (Microcoryphia and Zygentoma) from subterranean environments of Iran, with description of three new species + + + +Author + +Molero, Rafael + + + +Author + +Tahami, Mohadeseh Sadat + + + +Author + +Gaju, Miquel + + + +Author + +Sadeghi, Saber + +text + + +ZooKeys + + +2018 + +806 + + +17 +46 + + + + +http://dx.doi.org/10.3897/zookeys.806.27320 + +journal article +http://dx.doi.org/10.3897/zookeys.806.27320 +1313-2970-806-17 +A312BA3989FF4D43B6E206F880B956E6 +A312BA3989FF4D43B6E206F880B956E6 + + + + +Ctenolepisma (Sceletolepisma) targionii (Grassi & Rovelli, 1889) + + + +Studied material. +One male, mounted in a slide, two females and one juvenile in alcohol. Endogean zone in Dej Shapour cave, Kazerun, Fars Province, Iran. 21.X.2015. Deposited in UCO, Ref. Z2516. + + +Distribution and habitat. + +This species is widespread in the southern Palaearctic, but it is new for Iran. It is the first time that it has been recorded in the subterranean environment. +Ctenolepisma targionii +is found as a domestic form in the Western Palaearctic, but it lives in natural habitats in southwestern Asia, suggesting that it is native from the latter area. + + + +Discussion. + +Together with the above-described +Ctenolepisma subterraneum +, the number of species of this genus in Iran increases to nine; +C. targionii +represents the third species known for Iran of the subgenus +Sceletolepisma +. + + + + \ No newline at end of file diff --git a/data/38/05/7C/38057C80C887AC37950FD0C3866D07CC.xml b/data/38/05/7C/38057C80C887AC37950FD0C3866D07CC.xml new file mode 100644 index 00000000000..5f9f8d6e254 --- /dev/null +++ b/data/38/05/7C/38057C80C887AC37950FD0C3866D07CC.xml @@ -0,0 +1,126 @@ + + + +Flora der Schweiz und angrenzender Gebiete. Band 3. Plumbaginaceae bis Compositae (2 nd edition): Unterfamilie _ tubuliflorae + + + +Author + +Hess, Hans Ernst + + + +Author + +Landolt, Elias + + + +Author + +Hirzel, Rosmarie + +text + +1976 +Birkhaeuser Verlag + + +https://doi.org/10.5281/zenodo.292249 + +book +292249 +10.5281/zenodo.292249 +3-7643-0556-8 + + + +<subSubSection id="C288E0B8E198F18F32D08E92F14ADAB1" pageId="null" pageNumber="562" type="nomenclature"> +<paragraph id="A563D7226EE7AC94D700C242C42EBC3A" pageId="null" pageNumber="562"> +<taxonomicName id="ECD24E04DFEBB6BF67466D0201669CD1" authority="(DC.) F. Schultz" authorityName="F. Schultz" baseAuthorityName="DC." class="Magnoliopsida" family="Asteraceae" genus="Achillea" kingdom="Plantae" order="Asterales" pageId="null" pageNumber="562" phylum="Tracheophyta" rank="species" species="oxyloba"> +Achillea +<normalizedToken id="9A7AD965FC5897C5DD1609EAB000A039" originalValue="oxýloba" pageId="null" pageNumber="562">oxyloba</normalizedToken> +(DC.) F. Schultz +</taxonomicName> +</paragraph> +</subSubSection> +<subSubSection id="6BDAD00A246ECFA63CD8D65883875A27" pageId="null" pageNumber="562" type="reference_group"> +<paragraph id="24255649FD4CB876ABEF4AD7393DA3D5" pageId="null" pageNumber="562"> +( +<taxonomicName id="7EF224C6B7079AA0D52A7AFCF800A4AB" authority="L." authorityName="L." class="Magnoliopsida" family="Asteraceae" genus="Anthemis" kingdom="Plantae" order="Asterales" pageId="null" pageNumber="562" phylum="Tracheophyta" rank="species" species="alpina"> +<emphasis id="C2A868BE569EAEFED71CB1F18269CE95" italics="true" pageId="null" pageNumber="562">Anthemis alpina</emphasis> +<authorityName id="1CD46DB6F2E206871F2BD7BEA40E4EE1" pageId="null" pageNumber="562">L.</authorityName> +</taxonomicName> +) +</paragraph> +</subSubSection> +<subSubSection id="4DD81ACAC0EDD3786362E985C3F2FCA8" pageId="null" pageNumber="562" type="vernacular_names"> +<paragraph id="AC93AFDB21CD5C39644F153EEF881E23" pageId="null" pageNumber="562">Spitzblatt-Schafgarbe</paragraph> +</subSubSection> + + + +Ausdauernd, mit weit verzweigtem Rhizom und sterilen Blattrosetten; 8-25 cm hoch. Stengel aufrecht oder am Grunde bogig aufsteigend, einfach, unten kahl, oben zerstreut bis dicht behaart (Haare 0,5-1 mm lang). +Blaetter +im +Umriss +3-5mal so lang wie breit, bis zum Mittelnerv fiederteilig, jederseits mit 6-15 0,2-0,8 mm breiten, ungeteilten oder tief 3-5teiligen Zipfeln, zerstreut behaart. + +Koepfe +im Durchmesser 2 + +- +2,8 cm, einzeln +( +sehr selten zu 2 +) +am Stengel. +Huelle +6-8 mm lang. +Huellblaetter +wenig behaart, schwarz berandet. +Spreublaetter +kahl. +Zungenfoermige +Blueten +13-18, +weiss +; ausgebreiteter Teil meist +laenger +als die +Huelle +. +Fruechte +etwa 2 mm lang. - +Bluete +: Sommer. + + +Zytologische Angaben. 2n += +18: +Material aus den Dolomiten (Favarger 1965). + + +Standort. +Alpin, seltener subalpin. Steinige, kalkreiche +Boeden +. Felsen, Felsschutt, steinige Weiden. + + + +Verbreitung. +Suedostalpen-Pflanze +: + +Suedliche +Kalkalpen zwischen Ortlergebiet und +Kaernten +. - Im Gebiet: Ortler gebiet (vom Valle del Braulio +ostwaerts +). + + + + \ No newline at end of file diff --git a/data/38/06/63/380663D78499C64DAD75872F2CD59052.xml b/data/38/06/63/380663D78499C64DAD75872F2CD59052.xml new file mode 100644 index 00000000000..6dbf1876b19 --- /dev/null +++ b/data/38/06/63/380663D78499C64DAD75872F2CD59052.xml @@ -0,0 +1,125 @@ + + + +On the Lathrobium fauna of the Emei Shan, Sichuan, China (Coleoptera, Staphylinidae, Paederinae) + + + +Author + +Assing, Volker + + + +Author + +Peng, Zhong + + + +Author + +Zhao, Mei-Jun + +text + + +ZooKeys + + +2013 + +277 + + +47 +67 + + + + +http://dx.doi.org/10.3897/zookeys.277.4671 + +journal article +http://dx.doi.org/10.3897/zookeys.277.4671 +1313-2970-277-47 + + + + + +Lathrobium +conexum Assing & Peng + +sp. n. +Figs 2C511 + + + +Type material. + +Holotype ♂: 'CHINA: Sichuan Prov., Emeishan City, Mt. Emeishan, +29°33'N +, +103°23'E +, 27.vii.2012, alt. 1,100 m, Dai, Peng & Yin leg. / Holotypus ♂ +Lathrobium conexum +sp. n., det. Assing & Peng 2012' (SNUC). Paratypes: 2♂♂, 2♀♀: same data as holotype (SNUC). + + + +Etymology. + +The specific epithet (Latin, adjective: connected) refers to the merged ventral process and dorsal plate of the aedeagus and emphasizes the hypothesized close relationship of +Lathrobium conexum +to +Lathrobium iunctum +and +Lathrobium coniunctum +. + + + + +Description +. + + +Body length 8.8-10.0 mm; length of forebody: 4.1-4.5 mm. Habitus as in Fig. 2C. Head noticeably transverse, 1.05-1.10 times as broad as long. Other external characters as in +Lathrobium iunctum +. + +Male. Sternite VII (Fig. 5D) distinctly transverse and with relatively small, subelliptic, and shallow posterior impression in asymmetric position, this impression with defined and extensive cluster of numerous distinctly modified, short and stout black setae; posterior margin weakly convex. Sternite VIII (Fig. 5E) weakly transverse, with small and shallow impression in asymmetric position posteriorly, this impression with few short black setae; posterior excision shallow and in distinctly asymmetric position. Sternite IX as in Fig. 5F. Aedeagus (Figs 5G, H) approximately 1.4 mm long (from base to apex of dorsal plate) and distinctly asymmetric; ventral process and dorsal plate fused; basal portion of aedeagus small; internal sac with weakly sclerotized basal sclerite. +Female. Sternite VIII (Fig. 5B) oblong, its posterior margin strongly convex. Tergite IX with short and undivided median portion and with moderately long postero-lateral proce sses; tergite X approximately 2.3 times as long as tergite IX in the middle (Fig. 5C). + + +Comparative notes. + +As can be inferred from the similarly derived morphology of the aedeagus (ventral process and dorsal plate fused and distinctly asymmetric; small basal portion; internal sac with weakly sclerotized basal sclerite), the similar modifications of the male sternite VII (posterior impression in asymmetric position and with cluster of distinctly modified setae), the similar female secondary sexual characters, and the practically identical external characters, +Lathrobium conexum +is closely allied to +Lathrobium iunctum +and +Lathrobium coniunctum +. The similar modifications of the male sternite VIII would suggest that it may be most closely related to the latter. + + + +Distribution and natural history. + +This species is currently known only from the type locality. The specimens were collected by sifting leaf litter and humus from the floor of hardwood forest with +Kalopanax +at an altitude of 1,100 m (Fig. 11). + + + +Figure 5. +Lathrobium conexum +. A female tergite VIII B female sternite VIII C female tergites +IX-XD +male sternite VII E male sternite VIII F male sternite IX G aedeagus in lateral view H aedeagus in ventral view. Scale bars: 0.5 mm. + + + + + \ No newline at end of file diff --git a/data/38/06/77/3806778E61B36F810FCE704CCF0FDF94.xml b/data/38/06/77/3806778E61B36F810FCE704CCF0FDF94.xml new file mode 100644 index 00000000000..77bdef0e2fc --- /dev/null +++ b/data/38/06/77/3806778E61B36F810FCE704CCF0FDF94.xml @@ -0,0 +1,85 @@ + + + +Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea + + + +Author + +Dale-Skey, Natalie + + + +Author + +Askew, Richard R. + + + +Author + +Noyes, John S. + + + +Author + +Livermore, Laurence + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8013 +8013 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8013 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8013 +1314-2828--8013 + + + + +Paracentrobia Howard, 1897 + + + + +ABBELLA +Girault, 1911 + + +BRACHISTELLA +Girault, 1911 + + +JASSIDOPHTHORA +Perkins, 1912 + + +ABBELLISCA +Ghesquiere +, 1946 + + + + \ No newline at end of file diff --git a/data/38/06/87/380687CDFFDAFF82FF11FF52FD1AFE19.xml b/data/38/06/87/380687CDFFDAFF82FF11FF52FD1AFE19.xml new file mode 100644 index 00000000000..2278092e963 --- /dev/null +++ b/data/38/06/87/380687CDFFDAFF82FF11FF52FD1AFE19.xml @@ -0,0 +1,129 @@ + + + +A catalogue of the families Chrysolampidae, Eupelmidae, Eurytomidae, Leucospidae, Ormyridae, Perilampidae, Torymidae and Trichogrammatidae (Hymenoptera, Chalcidoidea) of Eritrea + + + +Author + +Madl, Michael + +text + + +Linzer biologische Beiträge + + +2023 + +55 + + +1 + + +287 +295 + + + +journal article +10.5281/zenodo.10787945 +0253-116X +10787945 + + + + + + + +Perilampus nimrodus +( +ARGAMAN + +, +1990) + + + + +Lufarfar nimrodus +sp.n. +: + +ARGAMAN +1990: 232 + +(key). + + + + +Lufarfar nimrodus +sp.n. +: + +ARGAMAN +1991: 4 + +(description + +, Assab), 13 (world catalogue: East Africa = +Eritrea +). + + + + + + +Perilampus nimrodus +( + +ARGAMAN +, 1990 + +) + +: + + +DARLING +1996: 125 + + +(taxonomy). + + + + +Perilampus nimrodus +( + +ARGAMAN +, 1990 + +) + +: +KIMSEY +& +BROTHERS +2016: 165 (catalogue species described by Q. Argaman). + +D i s t r i b u t i o n:Assab. + + + + +Perilampus nimrodus + +is known only from +Eritrea +. + + + + \ No newline at end of file diff --git a/data/38/06/87/380687CDFFDBFF83FF11FB6BFD71FA20.xml b/data/38/06/87/380687CDFFDBFF83FF11FB6BFD71FA20.xml new file mode 100644 index 00000000000..cb9adc74046 --- /dev/null +++ b/data/38/06/87/380687CDFFDBFF83FF11FB6BFD71FA20.xml @@ -0,0 +1,129 @@ + + + +A catalogue of the families Chrysolampidae, Eupelmidae, Eurytomidae, Leucospidae, Ormyridae, Perilampidae, Torymidae and Trichogrammatidae (Hymenoptera, Chalcidoidea) of Eritrea + + + +Author + +Madl, Michael + +text + + +Linzer biologische Beiträge + + +2023 + +55 + + +1 + + +287 +295 + + + +journal article +10.5281/zenodo.10787945 +0253-116X +10787945 + + + + + + + +Perilampus horocos +( +ARGAMAN + +, +1990) + + + + +Afroperilampus horocos +sp.n. +: + +ARGAMAN +1990: 206 + +(fig. 49), 210 (key), 212 (fig. 85), 246 + + + + +(description + +♁, Keren ( +paratype + +)). +Afroperilampus + +horocos + +ARGAMAN +, 1990 + + +: + +ARGAMAN +1991: 9 + +(world catalogue: East Africa). + +Perilampus horocos +( + +ARGAMAN +, 1990 + +) + +: + +DARLING +1996: 110-111 + +(taxonomy). + +Perilampus horocos +( + +ARGAMAN +, 1990 + +) + +: +KIMSEY +& +BROTHERS +2016: 164 (catalogue species described by Q. Argaman: only +Tanzania +: +Arusha +). + +D i s t r i b u t i o n:Keren. + + +Perilampus horocos + +is also recorded from +Tanzania +. + + + + \ No newline at end of file diff --git a/data/38/06/87/380687CDFFDBFF83FF11FF53FBAEFD9D.xml b/data/38/06/87/380687CDFFDBFF83FF11FF53FBAEFD9D.xml new file mode 100644 index 00000000000..067d75801c4 --- /dev/null +++ b/data/38/06/87/380687CDFFDBFF83FF11FF53FBAEFD9D.xml @@ -0,0 +1,153 @@ + + + +A catalogue of the families Chrysolampidae, Eupelmidae, Eurytomidae, Leucospidae, Ormyridae, Perilampidae, Torymidae and Trichogrammatidae (Hymenoptera, Chalcidoidea) of Eritrea + + + +Author + +Madl, Michael + +text + + +Linzer biologische Beiträge + + +2023 + +55 + + +1 + + +287 +295 + + + +journal article +10.5281/zenodo.10787945 +0253-116X +10787945 + + + + + + + +Leucospis tricolor +KIRBY + +, +1883 + + + + + + + + +Leucospis tricolor +KIRBY +, 1883 + +: + + +BOUČEK +1974: 106 + + +(key), 109 (fig. 150), 111 (figs 151-153), 126 (taxonomy, biology, Ghinda), 231 (host-parasitoid catalogue). + + + + +Leucospis tricolor +KIRBY +, 1883 + +: +MADL +& +SCHWARZ +2012: 1227 (catalogue Afrotropical region), 1235 (fig. 3). + + + +D i s t r i b u t i o n:Ghinda. + + +Leucospis tricolor + +is also recorded from the +Central African Republic +, +Democratic Republic of the Congo +, +Ethiopia +, +Kenya +, +Mozambique +, +Nigeria +, +Senegal +, +Sierra Leone +, +Somalia +, +South Africa +, +Sudan +, +Tanzania +(mainland, +Zanzibar +), +Uganda +, +Zambia +and +Zimbabwe +. Four species of +Megachilidae +are known as hosts ( + +Pachyanthidium bicolor + +(LEPELETIER DE SAINT- FARGEAU, 1841), + +Pachyanthidium cordatum +(SMITH, 1854) + +, + +Pseudoanthidium truncatum +(SMITH, 1854) + +and + +Serapista denticulata +(SMITH, 1854)) + +, of which only + +Pseudoanthidium truncatum + +is recorded from +Eritrea +( +MADL 2019: 1386 +). + + + + \ No newline at end of file diff --git a/data/38/06/87/380687CDFFDCFF84FF11FB5CFE39F9FD.xml b/data/38/06/87/380687CDFFDCFF84FF11FB5CFE39F9FD.xml new file mode 100644 index 00000000000..8628172e76b --- /dev/null +++ b/data/38/06/87/380687CDFFDCFF84FF11FB5CFE39F9FD.xml @@ -0,0 +1,144 @@ + + + +A catalogue of the families Chrysolampidae, Eupelmidae, Eurytomidae, Leucospidae, Ormyridae, Perilampidae, Torymidae and Trichogrammatidae (Hymenoptera, Chalcidoidea) of Eritrea + + + +Author + +Madl, Michael + +text + + +Linzer biologische Beiträge + + +2023 + +55 + + +1 + + +287 +295 + + + +journal article +10.5281/zenodo.10787945 +0253-116X +10787945 + + + + + + + +Leucospis africana +CAMERON + +, +1907 + + + + + + + + +Leucospis africana +CAMERON +, 1907 + +: + + +BOUČEK +1974: 102 + + +(key), 105 (figs 123-126), 106 (taxonomy, description ♁, biology, Adi Caie), 231 (host-parasitoid catalogue). + + + + +Leucospis africana +CAMERON +, 1907 + +: +MADL +& +SCHWARZ +2012: 1222 (catalogue Afrotropical region). + + + +D i s t r i b u t i o n:AdiCaie. + + +Leucospis africana + +is recorded from the Afrotropical ( +Burundi +, +Central African Republic +, +Democratic Republic of the Congo +, +Eritrea +, +Ethiopia +, +Ghana +, +Kenya +, +Lesotho +, +Malawi +, +Mozambique +, +Namibia +, +Nigeria +, +South Africa +, +Tanzania +, +Uganda +, +Zambia +, +Zimbabwe +) and Palaearctic ( +Saudi Arabia +) regions. None of the hosts ( +Megachilidae +: + +Megachile spinarum +COCKERELL, 1937 + +and + +Serapista denticulata +(SMITH, 1854)) + +is known from +Eritrea +( +MADL 2019 +). + + + + \ No newline at end of file diff --git a/data/38/06/87/380687CDFFDDFF85FF11FB22FD71FA6C.xml b/data/38/06/87/380687CDFFDDFF85FF11FB22FD71FA6C.xml new file mode 100644 index 00000000000..7bcfbd0bb9c --- /dev/null +++ b/data/38/06/87/380687CDFFDDFF85FF11FB22FD71FA6C.xml @@ -0,0 +1,112 @@ + + + +A catalogue of the families Chrysolampidae, Eupelmidae, Eurytomidae, Leucospidae, Ormyridae, Perilampidae, Torymidae and Trichogrammatidae (Hymenoptera, Chalcidoidea) of Eritrea + + + +Author + +Madl, Michael + +text + + +Linzer biologische Beiträge + + +2023 + +55 + + +1 + + +287 +295 + + + +journal article +10.5281/zenodo.10787945 +0253-116X +10787945 + + + + + + + +Eurytoma spermophaga +SILVESTRI + +, +1915 + + + + + + + + +Eurytoma spermophaga + +sp.n. +: + + +SILVESTRI +1915b: 337 + + +(description + +♁, biology, Nefasit), 338 (figs 1.1-6). + + + + + +Eurytoma spermophaga +SILVESTRI +, 1915 + +: + + +MASI +1940: 280 + + +(catalogue Afrotropical region), 281 (biology). + + + + +Eurytoma spermophaga +SILVESTRI +, 1915 + +: +GATES +& +DELVARE +2008: 13 (taxonomy, Nefasit, catalogue Afrotropical region), 23 (tab. 1: parasitoid-host catalogue Afrotropical region). + + + +D i s t r i b u t i o n:Nefasit. + + +Eurytoma spermophaga + +is known only from +Eritrea +. + + + + \ No newline at end of file diff --git a/data/38/06/87/380687CDFFDDFF85FF11FCCFFB93FBB8.xml b/data/38/06/87/380687CDFFDDFF85FF11FCCFFB93FBB8.xml new file mode 100644 index 00000000000..4b5dbd52794 --- /dev/null +++ b/data/38/06/87/380687CDFFDDFF85FF11FCCFFB93FBB8.xml @@ -0,0 +1,165 @@ + + + +A catalogue of the families Chrysolampidae, Eupelmidae, Eurytomidae, Leucospidae, Ormyridae, Perilampidae, Torymidae and Trichogrammatidae (Hymenoptera, Chalcidoidea) of Eritrea + + + +Author + +Madl, Michael + +text + + +Linzer biologische Beiträge + + +2023 + +55 + + +1 + + +287 +295 + + + +journal article +10.5281/zenodo.10787945 +0253-116X +10787945 + + + + + + + +Eurytoma oleae +SILVESTRI + +, +1915 + + + + + + + + +Eurytoma oleae + +sp.n. +: + + +SILVESTRI +1915a: 275 + + +(description + +♁, fig. 30, biology, Nefasit), 276 (figs 31.1-10), 277 (fig. 32). + + + + + +Eurytoma oleae +SILVESTRI +, 1915 + +: + + +MASI +1940: 280 + + +(catalogue Afrotropical region), 281 (biology). + + + + + +Eurytoma oleae +SILVESTRI +, 1915 + +: + + +THOMPSON +1944: 103 + + +(world host-parasitoid catalogue). + + + + + +Eurytoma oleae +SILVESTRI +, 1915 + +: + + +THOMPSON +1955: 328 + + +(world parasitoid-host catalogue). + + + + + +Eurytoma oleae +SILVESTRI +, 1915 + +: + + +DOMENICHI +2002: 305 + + +(taxonomy, +Eritrea +without exact locality). + + + + +Eurytoma oleae +SILVESTRI +, 1915 + +: +GATES +& +DELVARE +2008: 12 (taxonomy, biology, Nefasit, catalogue Afrotropical region), 23 (tab. 1: parasitoid-host catalogue Afrotropical region). + + + +D i s t r i b u t i o n:Nefasit. + + +Eurytoma oleae + +, a phytophagous species on olives, is also recorded from +South Africa +. + + + + \ No newline at end of file diff --git a/data/38/06/87/380687CDFFDDFF85FF11FDBBFD1EFCDF.xml b/data/38/06/87/380687CDFFDDFF85FF11FDBBFD1EFCDF.xml new file mode 100644 index 00000000000..88d1771ecac --- /dev/null +++ b/data/38/06/87/380687CDFFDDFF85FF11FDBBFD1EFCDF.xml @@ -0,0 +1,107 @@ + + + +A catalogue of the families Chrysolampidae, Eupelmidae, Eurytomidae, Leucospidae, Ormyridae, Perilampidae, Torymidae and Trichogrammatidae (Hymenoptera, Chalcidoidea) of Eritrea + + + +Author + +Madl, Michael + +text + + +Linzer biologische Beiträge + + +2023 + +55 + + +1 + + +287 +295 + + + +journal article +10.5281/zenodo.10787945 +0253-116X +10787945 + + + + + + + +Eurytoma elongatula +SILVESTRI + +, +1915 + + + + + + + +Eurytoma elongatula + +sp.n. +: + +SILVESTRI +1915b: 339 + +(description + +♁, figs 2.1-5, biology, Nefasit). + +Eurytoma elongata +SILVESTRI +, 1915 + +: + +MASI +1940: 280 + +(catalogue Afrotropical region), 281 (biology). + +Eurytoma elongatula +SILVESTRI +, 1915 + +: +GATES +& +DELVARE +2008: 11 (taxonomy, Nefasit, catalogue + + +Afrotropical region as + +Eurytoma elongata + +), 22 (tab. 1: parasitoid-host catalogue Afrotropical region). + + + +D i s t r i b u t i o n:Nefasit. + + +Eurytoma elongatula + +is known only from +Eritrea +. + + + + \ No newline at end of file diff --git a/data/38/06/87/380687CDFFDEFF85FF11FAF9FD00FECB.xml b/data/38/06/87/380687CDFFDEFF85FF11FAF9FD00FECB.xml new file mode 100644 index 00000000000..36991728280 --- /dev/null +++ b/data/38/06/87/380687CDFFDEFF85FF11FAF9FD00FECB.xml @@ -0,0 +1,107 @@ + + + +A catalogue of the families Chrysolampidae, Eupelmidae, Eurytomidae, Leucospidae, Ormyridae, Perilampidae, Torymidae and Trichogrammatidae (Hymenoptera, Chalcidoidea) of Eritrea + + + +Author + +Madl, Michael + +text + + +Linzer biologische Beiträge + + +2023 + +55 + + +1 + + +287 +295 + + + +journal article +10.5281/zenodo.10787945 +0253-116X +10787945 + + + + + + + +Eupelmus spermophilus +SILVESTRI + +, +1915 + + + + + + + + +Eupelmus spermophilus + +sp.n. +: + + +SILVESTRI +1915a: 277 + + +(biology), 286 (keys ♁, + +), 287 (description + +♁, figs 42, 43.1-5, biology, Nefasit), 288 (fig. 44). + + + + +Eupelmus spermophilus +SILVESTRI +, 1915 + +: + +POWELL +et al. 2019: 186 + +(taxonomy), 187 (taxonomy), 189 (taxonomy, biology, +South Africa +), 190 (figs 4A, B), 194 (fig. 8: taxonomy), 195 (taxonomy, biology, +Eritrea +( + +SILVESTRI +1915a + +)). + + +D i s t r i b u t i o n:Nefasit. + +Eupelmus spermophilus + +, which is an olive seeed feeder (CALECA et al. 2019: 125; +POWELL et al. 2020: 441 +), is also known from +South Africa +. + + + + \ No newline at end of file diff --git a/data/38/06/CC/3806CC6D5A9F64AF761F9718449B3054.xml b/data/38/06/CC/3806CC6D5A9F64AF761F9718449B3054.xml new file mode 100644 index 00000000000..a136292d0e1 --- /dev/null +++ b/data/38/06/CC/3806CC6D5A9F64AF761F9718449B3054.xml @@ -0,0 +1,159 @@ + + + +Flora Helvetica - Brassicaceae + + + +Author + +Konrad Lauber + + + +Author + +Gerhart Wagner + + + +Author + +Andreas Gygax + +text + + +2018 +Haupt Verlag + +Bern + + + +Flora Helvetica + + + +480 +566 + + + +book chapter +978-3-258-08047-5 + + + + + +Lepidium densiflorum +Schrad. + + + + + +Artbeschreibung: Obere +Blaetter +lineal-lanzettlich, +gezaehnt +. + +Kronblaetter +meist fehlend, Fruchtstand sehr dicht + +, Fruchtstiele aufrecht abstehend, +Schoetchen +breit-oval, 2-2,5(-3) mm breit, mit enger Ausrandung, +fluegelartiger +Rand an den Samen +hoechstens +0,1 mm +breit. + + + + +Verbreitung global: +Urspruenglich +nordamerikanisch + + + + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl FtrockenLichtzahl LhellSalzzeichen--
Reaktionszahl Rschwach sauer bis neutral (pH 4.5-7.5)Temperaturzahl Twarm-kollin
+Naehrstoffzahl +N + +naehrstoffreich + +Kontinentalitaetszahl +K + +subozeanisch bis subkontinental (mittlere Luftfeuchtigkeit, +maessige +Temperaturschwankungen und +maessig +tiefe Wintertemperaturen) +
+
+
+ + +Volksname Deutscher Name: + +Dichtbluetige +Kresse + +Nom +francais +: + +Passerage +a +fleurs denses + +Nome italiano: +Lepidio densifloro + + +
+
\ No newline at end of file diff --git a/data/38/07/87/380787BD78028834FF3B1D3DFEC0E68A.xml b/data/38/07/87/380787BD78028834FF3B1D3DFEC0E68A.xml new file mode 100644 index 00000000000..d1c19ce4dd8 --- /dev/null +++ b/data/38/07/87/380787BD78028834FF3B1D3DFEC0E68A.xml @@ -0,0 +1,409 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Oreomela dubeshkoae +Medvedev, 1977 + + + + +(Fig. 2) + + + +References. +Medvedev and Voronova 1977a: + + +337, 349; Medvedev 1982: 257; +Kippenberg 2010: 430 +. + + + + +Material Examined. +Altan-Obo, +25-28.vii.1976 +, + + +leg. L. Medvedev and N. Voronova ( +LMC +); Baruun- + + + +Khargaityn-Gol, + +18–21.v.2015 + +, leg. +R. Yakovlev +( +EGC +) + +. + + + + +Distribution. +Mongolia +( +Hovd +). + + +Notes. + +Oreomela dubeshkoae + +is the sole repre- + + +sentative of + +Oreomela +s. str. + +in the Mongolian + + + +Altai. Medvedev (1977) described this species +Fig. 2. + +Oreomela dubeshkoae + +, female, western based upon a single young female. I have found +Mongolia +, +Hovd aimak +, +Bajtag-Bogdo Mts. +, +Baruunone +additional female. +Khargaityn-Gol +, + +18–21 May 2015 + +, leg. +R. Yakovlev +( +EGC +) + +. + + + + +Cystocnemis +Motschulsky, 1860 + + +(EGC); + +Arshantyn-Nuruu +, + +19.vii.2009 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +holotype +( +ISEA +), + + +Cystocnemis arnoldii +Lopatin, 1974 + + +paratypes +( +YuMC +, +EGC +)) + +. + + +Distribution. +Mongolia +( +Hovd +). + + + + +References. +Lopatin 1974: 176, 1975: 217; + + +Notes. +This species is known only from the Medvedev and Voronova 1977a: 336, 1978: 14; + + +Arshantyn-Nuruu mountain range on the southwest- Medvedev 1982: 257; +Kippenberg 2010: 429 +; + + +ern slopes of the Mongolian +Altai +. It may occur Mikhailov 2013: 310. + +also on other ranges of similar elevation in the adja- + + + +Material Examined. +Munkh-Khairkhan, 30. + + +cent part of the Chinese +Altai +. All beetles were colvii.1968, leg. Arnoldi ( +ZIN +); Ikh-Dhargalantyn- + + +lected under stones on mountain crests in the zone Gol, 5.vii.80, leg. L. Medvedev ( +ZIN +). + + +of highland steppes. It is endemic in +Mongolia +. + + + + +Distribution. +Mongolia +(Bayan-Ulegei, +Hovd +). + + +E +Kazakhstan +. + + + + +Cystocnemis +( +Entomomela +) +Jacobson, 1925 + + +Cystocnemis +( +Cystocnemis +) +levmedvedevi + + + + +Mikhailov and Gus +’ + +kova, 2013 + +Cystocnemis +( +Entomomela +) +oirata +(Jacobson, 1926) + + + + +Reference. +Mikhailov and Guskova 2013a: 540. +References. +Jacobson 1925: 242 +; Medvedev +Material Examined. +Arshantyn-Nuruu, 11–12. and Voronova 1979: 117; Medvedev 1982: 257; +vii.2007 +, leg. E.V. Guskova and R.V. Yakovlev +Kippenberg 2010: 429 +; Mikhailov 2013: 309. + + + + +Material Examined. + +Khara-Nuur +, + +22.vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Dzhelty-Ula +, + +22.vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Altai +( +BU +), + +23.vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Altai +( +BU +), + +23.vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Usvajn-Davaa +, + +24.vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Elt-Gol +, + +1–8.vii.2005 + +, leg. +R. Yakovlev +and +D. Ryzhkov +( +EGC +) + +. + + + + +Distribution. +Mongolia +(Bayan-Ulegei). +Russia +( +Altai +(South-Chuya mountain range, Ukok plateau)), E +Kazakhstan +. + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD78028835FF281FB5FE89E595.xml b/data/38/07/87/380787BD78028835FF281FB5FE89E595.xml new file mode 100644 index 00000000000..18f0a21b75a --- /dev/null +++ b/data/38/07/87/380787BD78028835FF281FB5FE89E595.xml @@ -0,0 +1,108 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Entomoscelis adonidis +(Pallas, 1771) + + + + + + + +References. +Cherepanov 1956: 60 +; Medvedev + +and Dubeshko 1974: 191; Medvedev and Voronova +1977a: 336, 1979: 117; Medvedev 1982: 256; + +Kippenberg 2010: 428 +. + + + + +Material Examined. +Elt-Gol, +1–8.vii.2005 +, + + +leg. R. Yakovlev and D. Ryzhkov ( +EGC +). + + + + +Distribution. +Mongolia +(Bayan-Ulegei (new + + +aimak record), +Hovd +, Ubsunur, +Arkhangai +). Europe, + + +Kazakhstan +, +Russia +(European part, Siberia), + + +Japan +, +China +, N Africa. + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD78038834FF531DD3FD7EE3E6.xml b/data/38/07/87/380787BD78038834FF531DD3FD7EE3E6.xml new file mode 100644 index 00000000000..238b1a46ac7 --- /dev/null +++ b/data/38/07/87/380787BD78038834FF531DD3FD7EE3E6.xml @@ -0,0 +1,83 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Gonioctena +( +Gonioctena +) +linnaeana +Schrank, 1781 + + + + + + + +References. +Medvedev and Voronova 1976: 228; Medvedev 1982: 252; +Kippenberg 2010: 433 +. + + + + +Distribution. +Mongolia +(Bayan-Ulegei, Central). Europe except for Mediterranean, Caucasus, +Kazakhstan +except for southern parts, +Russia +(European part, W and S Siberia, +Altai +, +Tuva +). + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD78098839FD261B5DFF46E7E3.xml b/data/38/07/87/380787BD78098839FD261B5DFF46E7E3.xml new file mode 100644 index 00000000000..26efb25e29f --- /dev/null +++ b/data/38/07/87/380787BD78098839FD261B5DFF46E7E3.xml @@ -0,0 +1,121 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Crosita kowalewskyi matronula +Weise, 1894 + + + + + + + +References. +Weise 1894: 155; +Jacobson, 1899: 200 +; +Lopatin 1966: 233 +, +1968: 211 +, +1975: 207 +; +Medvedev 1976: 909 +, 1982: 248; Medvedev and Voronova 1976: 226, 1977b: 219, 1979: 110; +Kippenberg 2010: 421 +. + + + + +Material Examined. + +Tolbo, + +24.vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +); Dzhun- Zhargalant-Hajirkhan, + +28.vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +. + + + + +Distribution. +Mongolia +( +Gobi-Altai +, +Bayankhongor +, Uverhangay, Central). + + +Notes. +This is an endemic species in +Mongolia +. + +124 + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD7809883EFCE31F86FB52E41E.xml b/data/38/07/87/380787BD7809883EFCE31F86FB52E41E.xml new file mode 100644 index 00000000000..009527d9935 --- /dev/null +++ b/data/38/07/87/380787BD7809883EFCE31F86FB52E41E.xml @@ -0,0 +1,187 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Crosita elegans +Lopatin, 1968 + + + + + + + +References. +Lopatin 1968: 216 +, +1975: 207 +; +Medvedev 1976: 909 +, 1982: 247; Medvedev and Voronova 1977a: 331, 1979: 109; Medvedev and Zaitzev 1977a: 52; +Kippenberg 2010: 420 +. + + + + +Material Examined. + +Turgen-Gol +, 1–2.viii.75, leg. +L. Medvedev +( +LMC +) + +; + +Dzhun-Zhargalant- +Hajirkhan +, + +28.vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Must +, 30.vii.76, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Bidzh-Altai +, + +6-7.viii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Burgyn- +Davaa +, + +7.viii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Mogoijn-Gol +, + +8.vii.2010 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +; + +Hara-Adzragyn-Nuru, + +13– 14.vii.2010 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +. + + + + +Distribution. +Mongolia +(Bayan-Ulegei, +Hovd +, +Gobi-Altai +, Ubsunur). + + +Notes. +This is an endemic species in +Mongolia +. + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD7809883EFD381D9AFC60E242.xml b/data/38/07/87/380787BD7809883EFD381D9AFC60E242.xml new file mode 100644 index 00000000000..f862508ede4 --- /dev/null +++ b/data/38/07/87/380787BD7809883EFD381D9AFC60E242.xml @@ -0,0 +1,162 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Crosita kowalewskyi kowalewskyi +(Gebler, 1836) + + + + + + + +References. +Jacobson 1898: 200 +; +Lopatin 1968: 211 +, +1975: 207 +; +Medvedev 1976: 909 +, +1979: 164 +, 1982: 247; Medvedev and Voronova 1976: 226, 1977a: 331, 1978: 13, 1979: 109; Medvedev and Zaitzev 1977a: 52, 1978: 100; +Kippenberg 2010: 420 +. + + + + +Material Examined. + +Dutijn-Dava +, + +14.vii.1970 + +, leg. +Kozlov +( +ABC +) + +; + +Khalyun +, + +17.viii.1973 + +, ( +ABC +) + +; + +Dutijn- +Dava +, 12.vii.75, leg. +L. Medvedev +( +LMC +) + +; + +Hara- +Adzragyn-Nuru +, + +13–14.vii.2010 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +; + +Zhargalan +, + +19–21. vii.2010 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +. + + + + +Distribution. +Mongolia +(Bayan-Ulegei, +Hovd +, +Gobi-Altai +, +Bayankhongor +, South Gobi). +Russia +(S +Altai +), NW +China +. + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD7809883EFEF01C4BFEE3E368.xml b/data/38/07/87/380787BD7809883EFEF01C4BFEE3E368.xml new file mode 100644 index 00000000000..ffcaad2f2f4 --- /dev/null +++ b/data/38/07/87/380787BD7809883EFEF01C4BFEE3E368.xml @@ -0,0 +1,182 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Crosita altaica +(Gebler, 1823) + + + + + + + +References. +Lopatin 1968: 212 +, +1975: 206 +; +Medvedev 1976: 906 +, 1982: 246; Medvedev and Zaitzev 1977a: 52, 1978: 100; +Kippenberg 2010: 420 +. + + + + +Material Examined. + +Uench +, + +2.vii.1966 + +( + +615) leg. +Dr. Z. Kaszab +( +DEI +) + +; + +55 km +NE +Altai +, + +30. vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Arshantyn-Nuruu +, + +6-7.v.2002 + +, leg. +R. Yakovlev +( +EGC +) + +; + +Middle Bulgan-gol +, + +15.v.2002 + +, leg. +R. Yakovlev +and +D. Ryzhkov +( +EGC +) + +; + +Alag-Nuur +, + +12.vii.2009 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +; + +Arshantyn- +Nuruu +, + +15-17.v.2012 + +, leg. +R. Yakovlev +( +EGC +) + +. + + + + +Distribution. +Mongolia +(Bayan-Ulegei, +Hovd +, +Bayankhongor +). +Russia +( +Altai +), central and eastern +Kazakhstan +, Tarbagatay, central Tian-Shan, western +China +. + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD7809883EFF3B184CFB56E62D.xml b/data/38/07/87/380787BD7809883EFF3B184CFB56E62D.xml new file mode 100644 index 00000000000..ac81796144c --- /dev/null +++ b/data/38/07/87/380787BD7809883EFF3B184CFB56E62D.xml @@ -0,0 +1,109 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Crosita clementzae atasica +Medvedev, 1976 + + + + + + + +References. +Medvedev 1976: 908 +, 1982: 247; Medvedev and Voronova 1977a: 331; +Kippenberg 2010: 420 +. + + + + +Material Examined. + +Dzegijn-Ama + +7.viii.1968 + +, leg. +Emelyanov +( +ABC +); Atas-Ula, + +17.ix.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +. + + + + +Distribution. +Mongolia +( +Gobi-Altai +). + + +Notes. +An endemic species of +Mongolia +, described by +Medvedev (1976) +from the Atas-Ula Mountains. + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD7809883EFF441A4CFD7AE16B.xml b/data/38/07/87/380787BD7809883EFF441A4CFD7AE16B.xml new file mode 100644 index 00000000000..97ec897ccf4 --- /dev/null +++ b/data/38/07/87/380787BD7809883EFF441A4CFD7AE16B.xml @@ -0,0 +1,189 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Crosita clementzae clementzae +Jacobson, 1899 + + + + + + + +References. +Jacobson 1899: 9 +; +Lopatin 1975: 207 +; +Medvedev 1976: 908 +, 1982: 246; Medvedev and Voronova 1977a: 331, 1978: 14, 1979: 109; Medvedev and Zaitzev 1977a: 52; +Kippenberg 2010: 420 +. + + + + +Material Examined. + +Tachtoi-Ula +, + +1-8.vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Tsargin +, + +19-21.vii.1975 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Uenchin-Gol +, + +6.vii.2007 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +; + +Barangijn-Shara-Nuruu, + +11.vii.2007 + +leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +; + +Tsengel +, + +21.vii.2007 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +; + +Baruun-Khargaityn-Gol, + +18-21.v.2015 + +, leg. +R.V. Yakovlev +( +EGC +) + +; + +Gushoot- +Shineetijn-Gol +, + +23-26.v.2015 + +, leg. +R. Yakovlev +( +EGC +) + +. + + + + +Distribution. +Mongolia +(Bayan-Ulegei (new aimak record), +Hovd +, +Gobi-Altai +). +China +( +Xinjiang +). + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD780D8835FD3B184CFEE2E62D.xml b/data/38/07/87/380787BD780D8835FD3B184CFEE2E62D.xml new file mode 100644 index 00000000000..08ed2cdc0e7 --- /dev/null +++ b/data/38/07/87/380787BD780D8835FD3B184CFEE2E62D.xml @@ -0,0 +1,92 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Chrysomela +( +Chrysomela +) +tremula +Fabricius, 1787 + + + + + + + +References. +Jacobson 1909: 24 +; Medvedev and Dubeshko 1974: 191; +Lopatin 1975: 216 +; Medvedev and Voronova 1977a: 336, 1979: 114; + +128 Medvedev and Zaitzev 1978: 105; Medvedev + +1982: 254; +Kippenberg 2010: 391 +. + + + + +Distribution. +Mongolia +( +Hovd +, Ubsunur, + + +Arkhangai, Bulgan, Selenge +, Central, +Hentiy +, Eastern). + +Widespread in the Palearctic Region except for +Middle Asia. + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD780D883AFD341A04FCBDE153.xml b/data/38/07/87/380787BD780D883AFD341A04FCBDE153.xml new file mode 100644 index 00000000000..47f42b80f03 --- /dev/null +++ b/data/38/07/87/380787BD780D883AFD341A04FCBDE153.xml @@ -0,0 +1,153 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Chrysomela +( +Chrysomela +) +saliceti +(Weise, 1884) + + + + + + + +References. +Cherepanov 1956: 59 +; Medvedev and Dubeshko 1974: 191; +Lopatin 1975: 216 +; Medvedev and Voronova 1976: 336, 1979: 114; Medvedev and Zaitzev 1978: 105; Medvedev 1982: 254; +Kippenberg 2010: 391 +. + + + + +Material Examined. + +Tachtoi-Ula +, + +1–8.viii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Dod-Naryin-gol, + +26.vi.2005 + +, leg. +R. Yakovlev +and +D. Ryzhkov +( +EGC +) + +; + +Darkhijn-Shurag-Gol, + +26.v.2011 + +, leg. +R. Yakovlev +( +EGC +) + +; + +Darkhijn-Shurag-Gol, + +13.vi.2011 + +, leg. +R. Yakovlev +( +EGC +) + +. + + + + +Distribution. +Mongolia +( +Hovd +, Ubsunur, +Arkhangai +, Uverhangay, +Selenge +, Central, Eastern). Widespread in the Palearctic Region except for Middle Asia. + + +Notes. + +This species was previously recorded in +Hovd aimak +only for the ridge +Baytag-Bogdo. I +have found it in the other more northern localities of this aimak + +. + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD780D883AFD3A1C75FC9EE4A8.xml b/data/38/07/87/380787BD780D883AFD3A1C75FC9EE4A8.xml new file mode 100644 index 00000000000..4793f77e5f6 --- /dev/null +++ b/data/38/07/87/380787BD780D883AFD3A1C75FC9EE4A8.xml @@ -0,0 +1,119 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Chrysomela +( +Chrysomela +) +populi +Linnaeus, 1758 + + + + + + + +References. +Jacobson 1909: 24 +; +Cherepanov 1956: 59 +; +Lopatin 1966: 234 +, +1975: 216 +; Medvedev and Dubeshko 1974: 191; Medvedev and Voronova 1977a: 336; Medvedev 1982: 254; +Kippenberg 2010: 391 +. + + + + +Material Examined. + +Baruun-Khargaityn-Gol, + +18–21.v.2015 + +, leg. +R. Yakovlev +( +EGC +); Gushoot- Shineetijn-Gol, + +23–26.v.2015 + +, leg. +R. Yakovlev +( +EGC +) + +. + + + + +Distribution. +Mongolia +(Bayan-Ulegei, +Hovd +, Ubsunur, +Zavhan +, +Arkhangai +, Uverhangay, +Bulgan +, +Selenge +, Central, +Hentiy +). Widespread in the Palearctic Region. + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD780D883AFEFE1C00FEA0E375.xml b/data/38/07/87/380787BD780D883AFEFE1C00FEA0E375.xml new file mode 100644 index 00000000000..69a64f45351 --- /dev/null +++ b/data/38/07/87/380787BD780D883AFEFE1C00FEA0E375.xml @@ -0,0 +1,133 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Phaedon +( +Phaedon +) +armoraciae +(Linnaeus, 1758) + + + + + + + +References. +Lopatin 1966: 234 +, +1975: 214 +; Medvedev and Voronova 1977a: 334, 1979: 115; Medvedev and Zaitzev 1978: 112; Medvedev 1982: 248; +Kippenberg 2010: 396 +. + + + + +Material Examined. + +Dod-Naryin-gol, + +14.vii.2007 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +); Tsengel, + +25–27.vii.2010 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +. + + + + +Distribution. +Mongolia +(Bayan-Ulegei (new aimak record), +Hovd +, +Gobi-Altai +, Ubsunur, +Zavhan +, Khubsugul, +Arkhangai +, +Bulgan +, Central, +Hentiy +, Suhe Bator, Bayankhong, Uverhangay, South Gobi). N, Central, and E Europe, mountains of S +Kazakhstan +and Central Asia, +Russia +(European part, Siberia east to Yakutia). + + +Notes. +Adults and larvae feed on + +Hippuris + +L. ( +Plantaginaceae +). + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD780D883AFF1D1867FB58E690.xml b/data/38/07/87/380787BD780D883AFF1D1867FB58E690.xml new file mode 100644 index 00000000000..8c63a0d5e47 --- /dev/null +++ b/data/38/07/87/380787BD780D883AFF1D1867FB58E690.xml @@ -0,0 +1,137 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Sternoplatys clementzi +Jacobson, 1901 + + + + + + + +References. +Csiki 1901: 118 +; +Jacobson 1901: 131 +; + + +Lopatin 1964: 371 +, +1966: 234 +, 1967: 162, 1968: 213, 1970: 253, 1971: 227, 1975: 214; Mohr 1966: 368; Medvedev and Voronova 1977a: 335, 1979: 115; Medvedev and Zaitzev 1977b: 364, 1978: 109; Medvedev 1982: 249; +Kippenberg 2010: 394 +. + + + + +Material Examined. + +Tsengel, + +21.vii.2007 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +; + +Tsengel, + +26–30.vii.2009 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +; + +Tsengel, + +25–27.vii.2010 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +. + + + + +Distribution. +Mongolia +(Bayan-Ulegei, +Hovd +, Central, +Hentiy +, Eastern). +Russia +( +Altai +, +Tuva +, Yakutia). + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD780D883AFF441A26FE54E17E.xml b/data/38/07/87/380787BD780D883AFF441A26FE54E17E.xml new file mode 100644 index 00000000000..d61e3112cfc --- /dev/null +++ b/data/38/07/87/380787BD780D883AFF441A26FE54E17E.xml @@ -0,0 +1,158 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Phaedon +( +Phaedon +) +concinnus +Stephens, 1834 + + + + + + + +References. +Mohr 1966: 368; +Lopatin 1968: 213 +, +1975: 214 +; Medvedev and Dubeshko 1974: 190; +Kaszab 1977: 65 +; Medvedev Voronova 1977a: 334, 1979: 115; Medvedev and Zaitzev 1978: 112; Medvedev 1982: 248; +Kippenberg 2010: 397 +. + + + + +Material Examined. + +Arshantyn-Nuruu +, + +12.vii.2007 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +; + +Mogoijn-Gol +, + +11.vii.2009 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +; + +Hundijn-Gol +, + +3.vii.2010 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +; + +Mogoijn-Gol +, + +30–31.v.2011 + +, leg. +R. Yakovlev +( +EGC +) + +. + + + + +Distribution. +Mongolia +(Bayan-Ulegei, +Hovd +, +Gobi-Altai +(new aimak record), Ubsunur, +Zavhan +, Khubsugul, +Arkhangai +, +Bulgan +, Central, +Hentiy +, Bayankhong, Uverhangay, South Gobi). NNW and E Europe, Baltic States, +Russia +(N European part, N Siberia, Far East). + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD780F8838FCF51CA3FCCCE49C.xml b/data/38/07/87/380787BD780F8838FCF51CA3FCCCE49C.xml new file mode 100644 index 00000000000..4570fd8274b --- /dev/null +++ b/data/38/07/87/380787BD780F8838FCF51CA3FCCCE49C.xml @@ -0,0 +1,115 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Chrysolina +( +Pleurosticha +) +shapkini +Mikhailov and Gus + + +’ +kova, 2013 + + + +Reference. +Mikhailov and Guskova 2013a: 126. + + + + +Material Examined. + +Mankhan +, + +05.vii.2009 + +, leg. +E. Guskova +( +holotype +( +ISEA +), +paratypes +( +YuMC +and +EGC +). + + + + + +Distribution. +Mongolia +( +Hovd +). + + +Notes. +The +type +series was collected in the mountain breakstone steppe at +2,200 m +in the valley of the creek, under stones, at the base of bushes + +Salvia +sp. (Lamiaceae) + +. The species is endemic in +Mongolia +. + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD780F8838FD061A50FB51E215.xml b/data/38/07/87/380787BD780F8838FD061A50FB51E215.xml new file mode 100644 index 00000000000..90e1845baeb --- /dev/null +++ b/data/38/07/87/380787BD780F8838FD061A50FB51E215.xml @@ -0,0 +1,109 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Chrysolina +( +Pezocrosita +) +convexicollis +( +Jacobson, 1901 +) + + + + + + + +References. +Cherepanov 1956: 56 +; +Lopatin 1971: 225 +, +1975: 209 +; Medvedev and Voronova 1977a: 333, 1979: 112; Medvedev and Zaitzev 1977b: 363, 1978: 93; Medvedev 1982: 243; +Kippenberg 2010: 412 +. + + + + +Material Examined. + +Sagsaj, + +22.vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +. + + + + +Distribution. +Mongolia +(Bayan-Ulegei, +Hovd +, +Gobi-Altai +, Ubsunur, Khubsugul). +Russia +( +Tuva +). + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD780F8838FF181BADFEA1E1B0.xml b/data/38/07/87/380787BD780F8838FF181BADFEA1E1B0.xml new file mode 100644 index 00000000000..e80b77dde07 --- /dev/null +++ b/data/38/07/87/380787BD780F8838FF181BADFEA1E1B0.xml @@ -0,0 +1,109 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Chrysolina +( +Chalcoidea +) +brunnicornis +(Weise, 1887) + + + + + + + +References. +Weise 1887: 175; Medvedev and Voronova 1979: 112; Medvedev 1982: 244; +Kippenberg 2010: 402 +. + + + + +Material Examined. + +Tsengel +, + +26-30.vii.2009 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +); Tsengel, + +14.vii.2015 + +, leg. +R. Yakovlev +( +EGC +) + +. + + + + +Distribution. +Mongolia +(Bayan-Ulegei). +Russia +(SE +Altai +, +Tuva +). + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD780F8838FF471A4AFE0DE235.xml b/data/38/07/87/380787BD780F8838FF471A4AFE0DE235.xml new file mode 100644 index 00000000000..8e6991f99a4 --- /dev/null +++ b/data/38/07/87/380787BD780F8838FF471A4AFE0DE235.xml @@ -0,0 +1,94 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Chrysolina +( +Allohypericia +) +perforata simillima +Mohr, 1966 + + + + + + + +Material Examined. + +Tal-Nuur, + +10.vii.2015 + +, leg. +R.V. Yakovlev +( +EGC +) + +. + + + + +Distribution. +Mongolia +(Bayan-Ulegei (new aimak record), +Selenge +). + + +Notes. +This species is recorded here from the Mongolian +Altai +for the first time; it is previously reported only from +Selenge aimak +. + + + + \ No newline at end of file diff --git a/data/38/07/87/380787BD780F8838FF471FABFD7EE369.xml b/data/38/07/87/380787BD780F8838FF471FABFD7EE369.xml new file mode 100644 index 00000000000..c2932263cd8 --- /dev/null +++ b/data/38/07/87/380787BD780F8838FF471FABFD7EE369.xml @@ -0,0 +1,210 @@ + + + +The Chrysomelinae (Coleoptera: Chrysomelidae) of the Mongolian Altai + + + +Author + +Guskova, Elena V. + +text + + +The Coleopterists Bulletin + + +2017 + +2017-03-31 + + +71 + + +1 + + +120 +130 + + + + +http://dx.doi.org/10.1649/0010-065x-71.1.120 + +journal article +10.1649/0010-065X-71.1.120 +1938-4394 +4836543 + + + + + + + +Chrysolina +( +Allohypericia +) +perforata perforata +(Gebler, 1830) + + + + + + + +References. +Cherepanov 1956: 57 +; +Lopatin 1971: 224 +, +1975: 212 +; Medvedev and Korotyaev 1976: 244; Medvedev and Voronova 1977a: 333, 1979: 112; Medvedev and Zaitzev 1977b: 363, 1978: 92; Medvedev 1980: 317, 1982: 240; +Kippenberg 2010: 402 +. + + + + +Material Examined. + +Khara-Nuur +, + +22.vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Dzhelty-Ula +, + +22.vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Sagsaj +, + +23.vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Usvajn-Davaa +, + +24.vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Tolbo +, + +24.vii.1976 + +, leg. +L. Medvedev +and +N. Voronova +( +LMC +) + +; + +Tsengel +, + +26–30.vii.2009 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +; + +Zhargalan +, + +19–21.vii.2010 + +, leg. +E.V. Guskova +and +R.V. Yakovlev +( +EGC +) + +. + + + + +Distribution. +Mongolia +(Bayan-Ulegei, +Hovd +, +Gobi-Altai +(new aimak record), N +Zavhan +, N Khubsugul, E Ubsunur). +Russia +( +Altai +, +Khakassia +, +Tuva +, +Krasnoyarsk krai +, +Irkutsk region +, +Buryatia +). + + + + \ No newline at end of file diff --git a/data/38/07/CB/3807CB223E807EBEB081EF957F74F9A5.xml b/data/38/07/CB/3807CB223E807EBEB081EF957F74F9A5.xml new file mode 100644 index 00000000000..13621c60e83 --- /dev/null +++ b/data/38/07/CB/3807CB223E807EBEB081EF957F74F9A5.xml @@ -0,0 +1,72 @@ + + + +Guide to the Vascular Flora of the Savannas and Flatwoods of Shaken Creek Preserve and Vicinity (Pender & Onslow Counties, North Carolina, U. S. A.) + + + +Author + +Thornhill, Robert + + + +Author + +Krings, Alexander + + + +Author + +Lindbo, David + + + +Author + +Stucky, Jon + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1099 +1099 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1099 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1099 +1314-2828-2-1099 + + + + +Carex elliottii Schwein. & Torr. + + + +Distribution +Depressions in wet pine savannas (SPS-T), borrow pits, ditches. + + +Notes + +Infrequent. +May-Jun +. Thornhill 532, 1271 (NCSC). Specimens seen in the vicinity: Sandy Run [Hancock]: Taggart SARU 275 (WNC!). [= RAB, FNA, Weakley] + + + + \ No newline at end of file diff --git a/data/38/08/50/380850074BF1F19DD6DE302E3968A237.xml b/data/38/08/50/380850074BF1F19DD6DE302E3968A237.xml new file mode 100644 index 00000000000..553bbfacd6f --- /dev/null +++ b/data/38/08/50/380850074BF1F19DD6DE302E3968A237.xml @@ -0,0 +1,121 @@ + + + +Hornmilben (Oribatida) [pages 261 to 322] + + + +Author + +Weigmann, G. + + + +Author + +Miko, L. + +text + + +2006 +Goecke & Evers + +Keltern + + + +Hornmilben (Oribatida) [Dahl, Tierwelt Deutschlands, Teil 76] + + + +261 +322 + + + + +http://www.goeckeevers.de/verlag/dahl.html + +book chapter +Weigmann2006pp261to322 + + + + +Dissorhina +Hull, 1916 + + +Typ: +Eremaeus ornatus +Oudemans, 1900. - Syn. +Cosmoppia +Balogh, 1983. + + + + +1. Sensillus lang mit +schlank-keulenfoermigem +Kopf, ohne Rami oder Borsteln (gelegentlich +hoechstens +distal kurze Dornen). (+) Prodorsum mit Prodorsalgruben; Costulae und +Interbothridialwuelste +vorhanden, mit variabler Form. Rostrum-Mittelzahn +rautenfoermig +; +Koerperlaenge +250-350 µm. [141d-h] ..................................................................... +Dissorhina ornata +(Oudemans, 1900) + + +- Sensillus +dick-spindelfoermig +, einseitig mit Reihe von Rami besetzt. (+) Costulae kurz, undeutlich bis fehlend .........................................................................2 + + + +Abb +. 141: a) +Dissorhina tricarinatoides +: dorsal; b) Rostrumspitze mit Rostralborsten; c) Sensillus. - d) +D. ornata +: dorsal; e-f) +Varietaeten +der Prodorsum-Ausbildung; g) Rostrumspitze mit Rostralborsten; h) Sensillus. - i) +D. signata +: dorsal; k) Rostrumspitze mit Rostralborsten; l) Sensillus. - m) +Neotrichoppia confinis +: dorsal; n) Prodorsum-Teil, lateral; o) Borste am reduzierten Trochanter II; p-q) +Variabilitaet +des Sensillus. + + + +2. (1) Prodorsum ohne Costulae. Rostrum-Mittelzahn +laenglich +rautenfoermig +, deutlich vorstehend; +Koerperlaenge +195-235 µm. [141a-c] .............................................................. +Dissorhina tricarinatoides +(Dubinina, 1966) + + +- Costulae schwach entwickelt, als kurze gerade +Wuelste +hinter den Lamellarborsten; Rostrum-Mittelzahn dreieckig, nicht +ueber +die +Seitenzaehne +vorstehend; +Koerperlaenge +205-230 µm. [141i-l]........................................................ +Dissorhina signata +(Schwalbe, 1989) + + + + \ No newline at end of file diff --git a/data/38/08/62/3808620CFFE2A167FE2CF24AFE280320.xml b/data/38/08/62/3808620CFFE2A167FE2CF24AFE280320.xml new file mode 100644 index 00000000000..a6af64cbc93 --- /dev/null +++ b/data/38/08/62/3808620CFFE2A167FE2CF24AFE280320.xml @@ -0,0 +1,365 @@ + + + +Eustigmaeus mites from Turkey (Acari: Stigmaeidae) + + + +Author + +Sali + + + +Author + +Doğan, H + +text + + +Journal of Natural History + + +2005 + +2005-03-31 + + +39 + + +11 + + +835 +861 + + + + +http://dx.doi.org/10.1080/00222930400001558 + +journal article +10.1080/00222930400001558 +1464-5262 +4668774 + + + + + + +Eustigmaeus absens + +n. sp. + + + + + +( +Figures 8 +, +9 +) + + +Type materials + + + +Holotype +female and +94 paratype females +from moss and lichen on grassy soil, +Beğendik Village +, +Olur +, +Erzurum +, + +29 August 2001 + +. + + + +Female + + +Holotype +: length of body (excluding gnathosoma) 417, width 320. + + + +Figure 8. + +Eustigmaeus absens + +n. sp. +(female): (A) dorsal view; (B) dorsal ornamentation; (C) dorsal setae. + + + +Dorsum + + +Dorsal shields polygonally dimpled, dimples bearing fine punctations. Surface between dimples with a few fine punctations. Margins of dorsal shields and anterior edge of hysterosomal shield less sclerotized. Fossettes on dorsal shields as illustrated. Prodorsal shield with four pairs of setae and one pair of eyes. Hysterosomal shield with five pairs of setae, +e +2 +absent. Suranal shield with two pairs of setae. Dorsal body setae notched, with axial core. Postocular setae +sci +small. Setae +h +1 +and +h +2 +dissimilar to other dorsal body setae, densely notched, +h +1 +with core but +h +2 +without core. Dimensions of setae as follows: +υi +70, +υe +7, +sci +77, +sce +52, +c +1 +87, +c +2 +23, +d +1 +90, +d +2 +56, +e +1 +91, +f +1 +83, +h +1 +50, +h +2 +23. Distance between setae: +υi–υi +28, +υe–υe +127, +υi–υe +67, +sci–sci +207, +υe–sci +50, +sce–sce +297, +sci–sce +73, +c +1 +–c +1 +100, +d +1 +–d +1 +190, +c +1 +–d +2 +117, +c +1 +–d +1 +110, +c +1 +–f +1 +237, +d +2 +– +d +2 +300, +d +1 +– +d +2 +70, +e +1 +–e +1 +157, +d +1 +–e +1 +87, +d +1 +–f +1 +133, +f +1 +– f +1 +107, +e +1 +–f +1 +41, +h +1 +–h +1 +43, +h +2 +–h +2 +95, +h +1 +–h +2 +36. + + + +Figure 9. + +Eustigmaeus absens + +n. sp. +(female): (A) ventral view; (B) lateral view. + + + +Venter + + +Setae +c +2 +similar to +sci +, humeral shields with dimples. Humeral regions with major and minor callosities covered by dimples, incorporated in the margins of the dorsal shields. Coxisternal shields completely divided with polygonal dimples and bearing +1a +, +3a +and +4a +. Surface on coxae densely punctated and with faint reticulations. Aggenital shield with faint reticulations, two pairs of subequal setae. Pseudanal covers with fine punctations, three pairs of setae, subequal in length. Suranal shield ‘‘V’’-shaped with dimples. + + +Legs + + +Leg I 320, leg II 247, leg III 250, leg IV 300. Number of setae (solenidia in parentheses) on leg segments (I–IV) as follows: tarsi 14( +v +)-10( +v +)-8( +v +)-8( +v +), tibiae 7( +w +, +w +p)-6( +w +p)-6( +w +p)- 6( +w +p), genua 4( +k +)-4( +k +)-1-1, femora 6-5-3-2, trochanters 1-1-1-1, coxae 2-2-2-2. All tarsi with solenidion +v +. Lengths of solenidia on tarsi: +v +1 +23, +v +2 +17, +v +3 +6, +v +4 +4. Lengths of solenidia on tibiae: +w +8, +w +p +1 +16, +w +p +2 +13, +w +p +35 +w +p +4 +7. + + +Male + +Unknown. + +Etymology + + +The name of this new species, + +absens + +, refers to the absence of setae +e +2 +. + + +Remarks + + +This species is unique in that the hysterosomal shield bears five pairs of setae and trochanter III bears one seta. It may belong to a new genus, as numbers and positions of dorsal body setae are considered as generic significance. However, it seems prudent to await the descriptions of more species lacking setae +e +2 +, thus strengthening the generic significance of their character. + + + + \ No newline at end of file diff --git a/data/38/08/62/3808620CFFE3A17AFE9AF693FB5703BC.xml b/data/38/08/62/3808620CFFE3A17AFE9AF693FB5703BC.xml new file mode 100644 index 00000000000..7d6ccb61eeb --- /dev/null +++ b/data/38/08/62/3808620CFFE3A17AFE9AF693FB5703BC.xml @@ -0,0 +1,356 @@ + + + +Eustigmaeus mites from Turkey (Acari: Stigmaeidae) + + + +Author + +Sali + + + +Author + +Doğan, H + +text + + +Journal of Natural History + + +2005 + +2005-03-31 + + +39 + + +11 + + +835 +861 + + + + +http://dx.doi.org/10.1080/00222930400001558 + +journal article +10.1080/00222930400001558 +1464-5262 +4668774 + + + + + + +Eustigmaeus turcicus +Doğan and Ayyıldız, 2003 + + + + + + +( +Figure 7 +) + + + + + +Eustigmaeus turcicus +Doğan and Ayyıldız 2003, p 2115 + +. + + + + +Examined materials + + +Allotype +male and seven females from litter under + +Pinus + +sp., +Yozgat +, +7 September 2001 +; three females from soil and litter under + +Quercus + +sp., Karaçubuk village, Adaklı, +Bingöl +, +30 September 2001 +. + + + +Figure 7. + +Eustigmaeus turcicus +Doğan and Ayyıldız + +(male): (A) dorsal view; (B) ventral view. + + + +Male + + +Allotype +: length of body (excluding gnathosoma) 257, width 150. + + +Dorsum + + +Dorsal ornamentation as in female, fossettes on dorsal shields as illustrated. Propodosomal shield with four pairs of setae and one pair of eyes. Hysterosomal shield undivided, with six pairs of setae, suranal shield with two pairs of setae. Dorsal body setae long, unsheathed, with axial core, bilaterally spinulate. Setae +h +1 +and +h +2 +much shorter than others, with small spinules but without axial core. Dimensions of setae as follows: +υi +60, +υe +67, +sci +5 +sce +50, +c +1 +47, +c +2 +37, +d +1 +60, +d +2 +50, +e +15 + +e +2 +37 + +, +f +1 +53, +h +1 +26, +h +2 +20. Distance between setae: +υi–υi +23, +υe–υe +63, +υi–υe +30, +sci–sci +107, +υe–sci +26, +sce–sce +137, +sci–sce +33, +c +1 +–c +1 +43, +d +1 +–d +1 +53, +c +1 +–d +1 +37, +c +1 +–d +2 +50, +d +2 +– +d +2 +140, +d +1 +– +d +2 +47, +e +1 +–e +1 +63, +e +2 +–e +2 +117, +e +1 + +– +e + +2 +30, +d +1 + +– +e + +1 +48, +d +1 + +– +e + +2 +40, +d +2 + +– +e + +2 +50, +f +1 +–f +1 +37, +e +1 +–f +1 +28, +e +2 +–f +1 +60, +h +1 +–h +1 +17, +h +2 +–h +2 +37, +h +1 +–h +2 +8. + + +Venter + + +Setae +c +2 +on triangular humeral shields. Humeral regions without callosities. Coxisternal shields completely fused, +1a +, +3a +and +4a +present. Venter of ophistosoma with one pair of aggenital setae on aggenital shield. Pseudanal covers with three pairs of setae ( +ps +1, 2, 3 +). + + +Legs + + +Leg I 223, leg II 183, leg III 187, leg IV 203. Number of setae (solenidia in parentheses) on leg segments (I–IV) as follows: tarsi 15( +v +, +v„ +)-11( +v +, +v„ +)-9( +v +, +v„ +)-8( +v„ +); tibiae 7( +w +, +w +p)-6( +w +p)- 6( +w +p)-6( +w +p); genua 4( +k +)-4( +k +)-1-1; femora 6-4-3-2; trochanters 1-1-2-1; coxae 2-2-2-2. + + +Distribution + + +Turkey +(Doğan and Ayyıldız 2003). + + +Remarks + + +Adult male of + +E. turcicus + +was not known before. The male can be distinguished from female by the following features: dorsal body setae unsheathed, anogenital covers on posterior margin of idiosoma, with only one pair of aggenital setae, all tarsi with solenidion +v„ +and body smaller. + + + + \ No newline at end of file diff --git a/data/38/08/62/3808620CFFE7A17BFE8AF4A8FD4C0611.xml b/data/38/08/62/3808620CFFE7A17BFE8AF4A8FD4C0611.xml new file mode 100644 index 00000000000..edc02a77a50 --- /dev/null +++ b/data/38/08/62/3808620CFFE7A17BFE8AF4A8FD4C0611.xml @@ -0,0 +1,610 @@ + + + +Eustigmaeus mites from Turkey (Acari: Stigmaeidae) + + + +Author + +Sali + + + +Author + +Doğan, H + +text + + +Journal of Natural History + + +2005 + +2005-03-31 + + +39 + + +11 + + +835 +861 + + + + +http://dx.doi.org/10.1080/00222930400001558 + +journal article +10.1080/00222930400001558 +1464-5262 +4668774 + + + + + + +Eustigmaeus schusteri +( +Summers and Price, 1961 +) + + + + + + +( +Figures 5 +, +6 +) + + + + + +Ledermuelleria schusteri +Summers and Price 1961 +, p 379 + +. + + + +Ledermuelleria schusteri +: +Gerson 1972 +, p 330 + +. + + + +Eustigmaeus schusteri +: +Tseng 1982 +, p 37 + +. + + + + +Examined materials + + + +Sixty-seven +females and one deutonymph from moss and lichen on grassy soil, +Beğendik Village +, +Olur +, +Erzurum +, + +29 August 2001 + + +. + + +Female + +Length of body (excluding gnathosoma) 307–333, width 200–217. + +Dorsum + + +Dorsal shields covered with dimples and bearing fine punctations. Dorsal dimples nearly round, of uniform diameter except smaller around eyes and bases of setae. Surface between dimples with fine punctations. The margins of the dorsal shields and anterior surface of hysterosomal shield weakly sclerotized, faintly punctated, without dimples. Fossettes on dorsal shields as illustrated, indistinct in many specimens. Propodosomal shield with four pairs of setae and one pair of eyes. Hysterosomal shield with six pairs of setae. Suranal shield tucked under body with two pairs of setae. Dorsal body setae notched, with thin hyaline sheaths and pointed tips. Postocular setae +sci +very short. Setae +h +1 +and +h +2 +differ from other dorsal body setae, with spinules, but without sheaths. Dimensions of setae as follows: +υi +47, +υe +72, +sci +13, +sce +47, +c +1 +53, +c +2 +38, +d +1 +70, +d +2 +53, +e +1 +97, +e +2 +80, +f +1 +64, +h +1 +47, +h +2 +40. Distance between setae: +υi–υi +30, +υe–υe +83, +υi–υe +43, +sci–sci +147, +υe–sci +36, +sce–sce +183, +scisce +36, +c +1 +–c +1 +80, +d +1 +–d +1 +83, +c +1 +–d +2 +60, +c +1 +–d +1 +53, +d +2 +– +d +2 +190, +d +1 +– +d +2 +67, +e +1 +–e +1 +103, +e +2 +–e +2 +157, +e +1 + +– +e + +2 +40, +d +1 +–e +1 +83, +d +1 +–e +2 +64, +d +2 +–e +2 +70, +f +1 +–f +1 +73, +e +1 +–f +1 +30, +e +2 +–f +1 +73, +h +1 +–h +1 +30, +h +2 +–h +2 +77, +h +1 +–h +2 +24. + + + +Figure 5. + +Eustigmaeus schusteri +(Summers and Price) + +(female): (A) dorsal view; (B) ventral view; (C) dorsal ornamentation; (D) lateral view; (E) dorsal setae. + + + +Venter + + +Setae + +c +2 + +similar to other dorsal setae, placed on dimpled humeral shields. A pair of callosities associated with humeral shields. The callosities covered with dimples, some arranged like strung beads on central area, some arranged like pomegranate seeds. Coxisternal shields completely divided, with polygonal dimples and bearing +1a +, +3a +and +4a +. Surface on coxae densely punctated. Aggenital shield with polygonal dimples, two pairs of setae. Pseudanal shield covered with fine punctations, three pairs of subequal setae. Suranal shield ‘‘V’’-shaped. Humeral and suranal shields with similar patterns. + + + +Figure 6. + +Eustigmaeus schusteri +(Summers and Price) + +(deutonymph): (A) dorsal view; (B) lateral view. + + + +Legs + + +Leg I 253, leg II 203, leg III 220, leg IV 240. Number of setae (solenidia in parentheses) on leg segments (I–IV) as follows: tarsi 14( +v +)-10( +v +)-8( +v +)-8( +v +), tibiae 7( +w +, +w +p)-6( +w +p)-6( +w +p)- 6( +w +p), genua 4( +k +)-4( +k +)-1-1, femora 6-5-3-2, trochanters 1-1-2-1, coxae 2-2-2-2. All tarsi with solenidion +v +. Lengths of solenidia on tarsi: +v +1 +27, +v +2 +20, +v +3 +10, +v +4 +7. Lengths of solenidia on tibiae: +w +11, +w +p +1 +20, +w +p +2 +17, +w +p +3 +13, +w +p +4 +12. + + +Male + +Not observed. + +Deutonymph + +Length of body (excluding gnathosoma) 250, width 170. + +Dorsum + + +Dorsal shields covered with dimples and bearing fine punctations. Dorsal dimples as in female, but less sclerotized. Fossettes on dorsal shields indiscernible. Dorsal body setae as in female. Hysterosomal shield incompletely divided. Setae +h +1 +and +h +2 +dissimilar to other dorsal body setae, with spinules, without sheath. Dimensions of setae as follows: +υi +33, +υe +57, +sci +10, +sce +40, +c +1 +43, +c +2 +33, +d +1 +50, +d +2 +50, +e +1 +80, +e +2 +77, +f +1 +47, +h +1 +37, +h +2 +33. Distance between setae: +υi–υi +30, +υe–υe +70, +υi–υe +40, +sci–sci +113, +υe–sci +23, +sce–sce +150, +sci–sce +33, +c +1 +– c +1 +60, +d +1 +–d +1 +50, +c +1 +–d +2 +53, +c +1 +–d +1 +40, +d +2 +– +d +2 +157, +d +1 +– +d +2 +57, +e +1 +–e +1 +73, +e +2 +–e +2 +120, +e +1 + +– +e + +2 +33, +f +1 +–f +1 +50, +e +1 +–f +1 +23, +e +2 +–f +1 +57, +h +1 +–h +1 +20, +h +2 +–h +2 +56, +h +1 +–h +2 +23. + + +Venter + + +Ventral setae and features as in female, but dimples on humeral and coxisternal shields shallower, dimples on suranal and aggenital shields indiscernible. Ventral setae +4a +present, aggenital shield with two pairs of setae. + + +Legs + + +Leg I 210, leg II 170, leg III 157, leg IV 177. Number of setae (solenidia in parentheses) on leg segments (I–IV) as follows: tarsi 14( +v +)-10( +v +)-8( +v +)-8( +v +), tibiae 7( +w +, +w +p)-6( +w +p)-6( +w +p)- 6( +w +p), genua 4( +k +)-3( +k +)-0-0, femora 6-5-3-2, trochanters 1-1-2-0, coxae 2-2-2-2. Lengths of solenidia on tarsi: +v +1 +20, +v +2 +13, +v +35 +v +455 +. + + +Distribution + + +Canada +, +Taiwan +and +USA +( +Summers and Price 1961 +; +Gerson 1972 +; +Tseng 1982 +). +Remarks + + +This species was described and illustrated by +Summers and Price (1961) +, and was also recorded by +Gerson (1972) +from +Canada +and +Tseng (1982) +from +Taiwan +. General features and details of leg chaetotaxy of Turkish specimens are the same as in the +type +species given by +Summers and Price (1961) +. The deutonymph of this species, which is a new record for the Turkish fauna, is described for the first time. + + + + \ No newline at end of file diff --git a/data/38/08/62/3808620CFFE9A17FFE48F38AFDCB0424.xml b/data/38/08/62/3808620CFFE9A17FFE48F38AFDCB0424.xml new file mode 100644 index 00000000000..dd873705840 --- /dev/null +++ b/data/38/08/62/3808620CFFE9A17FFE48F38AFDCB0424.xml @@ -0,0 +1,433 @@ + + + +Eustigmaeus mites from Turkey (Acari: Stigmaeidae) + + + +Author + +Sali + + + +Author + +Doğan, H + +text + + +Journal of Natural History + + +2005 + +2005-03-31 + + +39 + + +11 + + +835 +861 + + + + +http://dx.doi.org/10.1080/00222930400001558 + +journal article +10.1080/00222930400001558 +1464-5262 +4668774 + + + + + + +Eustigmaeus kentingensis +Tseng, 1982 + + + + + + +( +Figure 4 +) + +Eustigmaeus kentingensis +Tseng 1982 +, p 25 + +. + + +Examined materials + + + +Three +females from soil and litter under + +Populus + +sp., +Kaledibi +, +Olur +, +Erzurum +, + +9 October 1999 + + +; + +one female from moss and lichen on stone, +Aziziye Redoubt +, +Erzurum +, + +28 April 2001 + + +; + +two females from soil from vineyard, +Elazıg +˘, + +8 September 2001 + +; +14 females + + +from soil and litter under + +Pinus + +sp., +Kırıkkale +, + +15 May 2002 + + +; + +six females from litter under + +Pinus + +sp., +Erbaa +, +Tokat +, + +15 May 2002 + + +; + +one female from grassy soil, Narman, +Erzurum +, + +23 May 2002 + + +; + +six females from grassy soil under an apple tree, +Oltu +, +Erzurum +, + +23 May 2002 + + +. + + +Female + +Length of body (excluding gnathosoma) 277, width 183. + + +Figure 4. + +Eustigmaeus kentingensis +Tseng + +(female): (A) dorsal view; (B) ventral view. + + + +Dorsum + + +Dorsal shields with oval and polygonal dimples, each dimple generally contains 16–25 vacuoles, a few with eight vacuoles. Fossettes on dorsal shields as illustrated. Propodosomal shield pointed anteriorly, with four pairs of setae and one pair of eyes. Hysterosomal shield with six pairs of setae, suranal shield with two pairs of setae. Dorsal body setae short, recurved and bushy. Dimensions of setae as follows: +υi +5 +υe +5 +sci +23, +sce +5 +c +1 +20, +c +2 +27, +d +15 +d +2 +23, +e +15 + +e +2 +27 + +, +f +1 +40, +h +15 +h +2 +30. Distance between setae: +υi–υi +33, +υe–υe +70, +υi–υe +33, +sci–sci +133, +υe–sci +37, +sce–sce +167, +sci–sce +37, +c +1 +–c +1 +70, +d +1 +–d +1 +60, +c +1 +–d +2 +63, +c +1 +–d +1 +50, +d +2 +– +d +2 +177, +d +1 +– +d +2 +60, +e +1 +–e +1 +67, +e +2 +–e +2 +143, +e +1 + +– +e + +2 +50, +d +1 + +– +e + +2 +53, +d +2 + +– +e + +2 +57, +f +1 +–f +1 +70, +e +1 +–f +1 +30, +e +2 +–f +1 +73, +h +1 +–h +1 +37, +h +2 +–h +2 +73, +h +1 +–h +2 +17. + + +Venter + + +Humeral setae + +c +2 + +similar to other dorsals. Humeral regions without callosities. Humeral and suranal shields with similar patterns. Coxisternal shields completely fused, reticulate with punctations, except central region of posterior coxisternal shield which has only punctations. Coxisternal shields bearing +1a +, +3a +and +4a +. Aggenital shield without dimples, with three pairs of setae, +ag +2 +and +ag +3 +subequal in length, but +ag +1 +slightly shorter than others. Pseudanal covers with three pairs of setae, subequal in length, +ps +1 +with spinules. + + +Legs + + +Leg I 177, leg II 160, leg III 153, leg IV 167. Number of setae (solenidia in parentheses) on leg segments (I–IV) as follows: tarsi 14( +v +)-10( +v +)-8( +v +)-7, tibiae 7( +w +, +w +p)-6( +w +p)-6( +w +p)- 6( +w +p), genua 4( +k +)-4( +k +)-1-1, femora 6-4-3-2, trochanters 1-1-2-1, coxae 2-2-2-2. +v +1 +. +v +2 +. +v +3 +, +v +4 +absent, femur II with four setae. + + +Male + +Not observed. + +Distribution + + +Taiwan +( +Tseng 1982 +). + + +Remarks + + +Oval, rectangular and triangular dorsal dimples, bushy dorsal body setae, and femur II with four setae are diagnostic characters of + +E. kentingensis + +. This species closely resembles + +E. anauniensis +( +Canestrini, 1889 +) + +, but can be distinguished from the latter by the shape of dimples on dorsum, + +E. anauniensis + +with polygonal dimples. In the Turkish specimens, the coxisternal shields are also reticulate with punctations, as in the +type +species, except for central region of posterior coxisternal shield where there are only punctations. This species is a new record for the Turkish fauna. + + + + \ No newline at end of file diff --git a/data/38/08/62/3808620CFFEBA171FEF1F605FEAE037F.xml b/data/38/08/62/3808620CFFEBA171FEF1F605FEAE037F.xml new file mode 100644 index 00000000000..2a8d2b09c47 --- /dev/null +++ b/data/38/08/62/3808620CFFEBA171FEF1F605FEAE037F.xml @@ -0,0 +1,373 @@ + + + +Eustigmaeus mites from Turkey (Acari: Stigmaeidae) + + + +Author + +Sali + + + +Author + +Doğan, H + +text + + +Journal of Natural History + + +2005 + +2005-03-31 + + +39 + + +11 + + +835 +861 + + + + +http://dx.doi.org/10.1080/00222930400001558 + +journal article +10.1080/00222930400001558 +1464-5262 +4668774 + + + + + + +Eustigmaeus jiangxiensis +Hu, Chen and Huang, 1996 + + + + + + +( +Figures 2 +, +3 +) + + + + + +Eustigmaeus jiangxiensis +Hu, Chen and Huang 1996 +, p 319 + +. + + + + +Examined materials + + + +Six +females from moss and lichen on bark, +Uzunoluk Forest +, +Oltu +, +Erzurum +, + +15 June 2001 + +; +50 females + + +from forest litter, +Uzunoluk +, +Oltu +, +Erzurum +, + +25 September 2001 + + +. + + +Female + +Length of body (excluding gnathosoma) 463, width 310. + + +Figure 2. + +Eustigmaeus jiangxiensis +Hu, Chen and Huang + +(female): (A) dorsal view; (B) ventral view; (C, D) dorsal setae. + + + + +Figure 3. + +Eustigmaeus jiangxiensis +Hu, Chen and Huang + +(female): (A) leg I; (B) leg IV. + + + +Dorsum + + +Reticulations covering dorsal shields consist of polygonal dimples. No visible fossettes on dorsal shields. Propodosomal shield with four pairs of setae and one pair of eyes. Hysterosomal shield with six pairs of setae, suranal shield with two pairs of setae. Dorsal body setae fusiform, apically pointed, slightly spinulated, with axial core and thin hyaline sheath. Setae +h +1 +and +h +2 +dissimilar to other dorsal body setae, with more spinules, without axial core and sheath. Dimensions of setae as follows: +υi +33, +υe +47, +sci +20, +sce +5 +c +1 +33, +c +2 +24, +d +1 +33, +d +2 +30, +e +15 + +e +2 +33 + +, +f +1 +53, +h +1 +40, +h +2 +37. Distance between setae: +υi–υi +33, +υe–υe +133, +υiυe +73, +sci–sci +220, +υe–sci +57, +sce–sce +270, +sci–sce +53, +c +1 +–c +1 +97, +d +1 +–d +1 +163, +c +1 +–d +2 +123, +c +1 +–d +1 +110, +d +2– +d +2 300, +d +1– +d +2 83, +e +1 +–e +1 130, +e +2 +–e +2 238, +e +1 +–e +2 67, +d +1 +–e +15 +d +2 +–e +2 110, +d +1 +–e +2 77, +f +1 +–f +1 80, +e +1 +– f +1 43, +e +2 +–f +1 117, +h +1 +–h +1 37, +h +2 +–h +2 97, +h +1 +–h +2 30. + + +Venter + + +Setae +c +2 +similar to other dorsals, placed on humeral shields ornamented with dimples. Humeral regions without callosities. Coxisternal shields completely divided, with polygonal dimples and bearing setae +1a +and +3a +, but +4a +absent. Surface on coxae with polygonal dimples. Aggenital shield with polygonal dimples, two pairs of setae, +ag +1 +slightly shorter than +ag +2 +. Pseudanal covers with three pairs of setae, +ps +3 +and +ps +2 +subequal in length, but +ps +1 +longer than others, rod-like and with minute spinules. + + +Legs + + +Leg I 310, leg II 263, leg III 267, leg IV 290. Number of setae (solenidia in parentheses) on leg segments (I–IV) as follows: tarsi 14( +v +)-10( +v +)-8( +v +)-7, tibiae 7( +w +, +w +p)-6( +w +p)-6( +w +p)- 6( +w +p), genua 4( +k +)-4( +k +)-1-1, femora 6-5-3-2, trochanters 1-1-2-1, coxae 2-2-2-2. +v +1 +. +v +2 +. +v +3 +, +v +4 +absent. + + +Distribution + + +China +( +Hu et al. 1996 +). + + +Remarks + + +This species is similar to +E. breυisetosa +( +Wood, 1966 +), from which it can be distinguished by the postocular setae +sci +which are not very diminutive. General features and details of leg chaetotaxy of Turkish specimens are as in the +type +species, given by +Hu et al. (1996) +, but the first pair of pseudanal setae ( +ps +1 +) with minute spinules. This species is a new record for the Turkish fauna. + + + + \ No newline at end of file diff --git a/data/38/08/62/3808620CFFEDA175FEE7F784FC2805EB.xml b/data/38/08/62/3808620CFFEDA175FEE7F784FC2805EB.xml new file mode 100644 index 00000000000..eb0a37f3b09 --- /dev/null +++ b/data/38/08/62/3808620CFFEDA175FEE7F784FC2805EB.xml @@ -0,0 +1,129 @@ + + + +Eustigmaeus mites from Turkey (Acari: Stigmaeidae) + + + +Author + +Sali + + + +Author + +Doğan, H + +text + + +Journal of Natural History + + +2005 + +2005-03-31 + + +39 + + +11 + + +835 +861 + + + + +http://dx.doi.org/10.1080/00222930400001558 + +journal article +10.1080/00222930400001558 +1464-5262 +4668774 + + + + + + +Eustigmaeus erciyesiensis +Doğan, Ayyıldız and Fan, 2003 + + + + + + + +Eustigmaeus erciyesiensis +Doğan, Ayyıldız and Fan 2003 +, p 132 + +. + + + + +Examined materials + + + +Three +hundred and fourteen females, five males and seven larvae from moss, +Ahmediye +, +Erzincan +, + +28 April 2001 + + +; + +two females from moss on bark, +Trabzon +, + +25 September 2002 + + +. + + +Distribution + + +Turkey +(Doğan et al. 2003). + + +Remarks + + + +This +species, collected from moss, at +Erciyes Mountain +, +Kayseri +, is common to the +Turkish +fauna. +General +features of specimens collected from +Trabzon +are as in the +type +species, but the major callosity is larger than that of the +type +specimens and indented + +. + + + + \ No newline at end of file diff --git a/data/38/08/62/3808620CFFEEA176FE2AF284FC7F0175.xml b/data/38/08/62/3808620CFFEEA176FE2AF284FC7F0175.xml new file mode 100644 index 00000000000..70d27668ef6 --- /dev/null +++ b/data/38/08/62/3808620CFFEEA176FE2AF284FC7F0175.xml @@ -0,0 +1,72 @@ + + + +Eustigmaeus mites from Turkey (Acari: Stigmaeidae) + + + +Author + +Sali + + + +Author + +Doğan, H + +text + + +Journal of Natural History + + +2005 + +2005-03-31 + + +39 + + +11 + + +835 +861 + + + + +http://dx.doi.org/10.1080/00222930400001558 + +journal article +10.1080/00222930400001558 +1464-5262 +4668774 + + + + + + +Eustigmaeus +Berlese, 1910 + + + + + + +Type +species: + +Stigmaeus kermesinus +Koch, 1841 + +. + +Body globular, dorsum with three unpaired shields, generally ornamented, humeral shields ventrolateral, paragenital shields with one to three pairs of setae, anogenital covers with three pairs of setae, palp with a tridentate, terminal eupathidium. + + + \ No newline at end of file diff --git a/data/38/08/62/3808620CFFF7A16DFE1AF474FB6204D4.xml b/data/38/08/62/3808620CFFF7A16DFE1AF474FB6204D4.xml new file mode 100644 index 00000000000..85101086cc8 --- /dev/null +++ b/data/38/08/62/3808620CFFF7A16DFE1AF474FB6204D4.xml @@ -0,0 +1,367 @@ + + + +Eustigmaeus mites from Turkey (Acari: Stigmaeidae) + + + +Author + +Sali + + + +Author + +Doğan, H + +text + + +Journal of Natural History + + +2005 + +2005-03-31 + + +39 + + +11 + + +835 +861 + + + + +http://dx.doi.org/10.1080/00222930400001558 + +journal article +10.1080/00222930400001558 +1464-5262 +4668774 + + + + + + +Eustigmaeus oacuus + +n. sp. + + + + + +( +Figure 15 +) + + +Type materials + + + +Holotype +female from moss under + +Quercus + +sp., +Erciyes Mountain +, +Kayseri +, + +16 May 2002 + +; one +paratype +female from dung hill, +Erzincan +, + +30 March 2001 + +. + + + +Female + + +Holotype +: length of body (excluding gnathosoma) 297, width 173. + + +Dorsum + + +Dorsal shields with shallow dimples, each dimple with about 10–16 circular or oval vacuoles, some of them bean-shaped, majority peripherally disposed, very few scattered centrally or irregularly dispersed. Fossettes on dorsal shields as illustrated. Propodosomal shield with four pairs of setae and one pair of eyes. Hysterosomal shield with six pairs of setae, suranal shield with two pairs of setae. Dorsal body setae short, fan-shaped with numerous spinules, except for setae +f +1 +which are longer and club-shaped. Dimensions of setae as follows: +υi +20, +υe +18, +sci +5 +sce +5 +c +1 +17, +c +2 +20, +d +15 +d +25 +e +15 + +e +2 +17 + +, +f +1 +30, +h +15 +h +2 +20. Distance between setae: +υi–υi +30, +υe–υe +70, +υi–υe +37, +sci–sci +120, +υe–sci +27, +sce–sce +147, +sci–sce +33, +c +1 +–c +1 +60, +d +1 +–d +1 +64, +c +1 +–d +1 +57, +c +1 +–d +2 +53, +d +2 +– +d +2 +157, +d +1 +– +d +2 +52, +e +1 + +– +e + +1 +53, +e +2 +–e +2 +123, +e +1 +–e +25 +d +1 + +– +e + +2 +40, +d +1 + +– +e + +1 +54, +d +2 +–e +2 +64, +f +1 +–f +1 +53, +e +1 +–f +1 +37, +e +2 +–f +1 +70, +h +1 +–h +1 +30, +h +2 +–h +2 +67, +h +1 +–h +2 +17. + + + +Figure 15. + +Eustigmaeus +υacuus + +n. sp. (female): (A) dorsal view; (B) ventral view; (C) leg I; (D) leg II; (E) leg III; (F) leg IV. + + + +Venter + + +Humeral shields triangular, setae +c +2 +, similar to other dorsals. Humeral regions without callosities. Humeral and suranal shields with similar patterns as dorsum. Coxisternal shields completely fused, with vacuoles, except for a central circular region on posterior coxisternal shield which is faintly punctate. Coxisternal shields bearing +1a +, +3a +and +4a +. Aggenital shield with three pairs of setae, +ag +2 +and +ag +3 +subequal in length, +ag +1 +slightly shorter than others. Pseudanal covers with three pairs of setae, subequal in length, +ps +1 +with spinules. Coxae, anal covers, coxisternal and aggenital shields with similar patterns. + + +Legs + + +Leg I 197, leg II 163, leg III 157, leg IV 190. Number of setae (solenidia in parentheses) on leg segments (I–IV) as follows: tarsi 14( +v +)-10( +v +)-8( +v +)-7, tibiae 7( +w +, +w +p)-6( +w +p)-6( +w +p)- 6( +w +p), genua 4( +k +)-4( +k +)-1-1, femora 6-4-3-2, trochanters 1-1-2-1, coxae 2-2-2-2. Lengths of solenidia on tarsi: +v +1 +18, +v +2 +10, +v +3 +4, femur II with four setae. + + +Male + +Unknown. + +Etymology + + +The name of this new species, +υacuus +, refers to the ornamentation of the dorsal and ventral shields. + + +Remarks + + +This species is similar to + +E. erzurumensis + +n. sp. +, + +E. anauniensis +( +Canestrini, 1889 +) + +and + +E. kentingensis +Tseng, 1982 + +, in the number of setae on femur II. However, it can be distinguished from these species by the shape of the dorsal dimples and the ventral shields. + + + + \ No newline at end of file diff --git a/data/38/08/62/3808620CFFFBA16FFE36F5AFFF490470.xml b/data/38/08/62/3808620CFFFBA16FFE36F5AFFF490470.xml new file mode 100644 index 00000000000..0c18145d4d0 --- /dev/null +++ b/data/38/08/62/3808620CFFFBA16FFE36F5AFFF490470.xml @@ -0,0 +1,608 @@ + + + +Eustigmaeus mites from Turkey (Acari: Stigmaeidae) + + + +Author + +Sali + + + +Author + +Doğan, H + +text + + +Journal of Natural History + + +2005 + +2005-03-31 + + +39 + + +11 + + +835 +861 + + + + +http://dx.doi.org/10.1080/00222930400001558 + +journal article +10.1080/00222930400001558 +1464-5262 +4668774 + + + + + + +Eustigmaeus fani + +n. sp. + + + + + +( +Figures 12–14 +) + + +Type materials + + + +Eleven +females from moss on soil, +Yukarı Parmaksız +, +Hınıs +, +Erzurum +, + +19 May 2000 + + +; + +six females and two males from soil and litter under + +Pinus +sylυestris + +, + +Deve Mountain +, I + +˙˙spir, +Erzurum +, + +4 August 2001 + + +. + + +Female + + +Holotype +: length of body (excluding gnathosoma) 423, width 277. + + +Dorsum + + +Dorsal shields slightly sclerotized, bearing fine punctations and round dimples, uniform in size. Dorsal dimples faint or shallow, only those on marginal area of dorsal shields discernible. No visible fossettes on dorsal shields. Propodosomal shield with four pairs of setae and one pair of eyes. Hysterosomal shield with six pairs of setae, suranal shield with two pairs of setae. Dorsal body setae slightly spinulated, with acute tips, hyaline sheath and very slender axial core, difficult to identify in some specimens. Setae +h +1 +and +h +2 +similar to other dorsals, but with more obvious spinules. Dimensions of setae as follows: +υi +50, +υe +55, +sci +5 +sce +47, +c +1 +50, +c +2 +25, +d +1 +47, +d +2 +43, +e +15 +f +1 +60, + +e +2 +50 + +, +h +1 +43, +h +2 +33. Distance between setae: +υi–υi +30, +υe–υe +110, +υi–υe +57, +sci–sci +187, +υe–sci +50, +sce–sce +240, +sci–sce +57, +c +1 +–c +1 +107, +d +1 +–d +1 +163, +c +1 +–d +2 +90, +c +1 +–d +1 +103, +d +2 +– +d +2 +267, +d +1 +– +d +2 +77, +e +1 +–e +1 +167, +e +2 +–e +2 +240, +e +1 +–e +2 +74, +d +1 +–e +15 +d +2 +–e +2 +90, +d +1 + +– +e + +2 +43, +f +1 +–f +1 +117, +e +1 +–f +1 +37, +e +2 +–f +1 +113, +h +1 +–h +1 +33, +h +2 +–h +2 +97, +h +1 +–h +2 +33. + + +Venter + + +Humeral shields smooth or with faint round dimples, bearing setae +c +2 +. Humeral setae approximately half as long as preocular setae +υe +. Humeral regions with major and minor callosities. The callosities finely punctate, not conjunct with margins of dorsal shields. Surface of coxae densely punctate, without apparent reticulum. Coxisternal shields completely divided, with polygonal dimples and with +1a +, +3a +and +4a +. Aggenital shield with polygonal dimples and three pairs of subequal setae. Pseudanal covers with three pairs of subequal setae. Suranal shields smooth or weakly dimpled. + + + +Figure 12. + +Eustigmaeus fani + +n. sp. +(female): (A) dorsal view; (B) ventral view; (C) lateral view. + + + +Legs + + +Leg I 267, leg II 217, leg III 217, leg IV 253. Number of setae (solenidia in parentheses) on leg segments (I–IV) as follows: tarsi 14( +v +)-10( +v +)-8( +v +)-8( +v +), tibiae 7( +w +, +w +p)-6( +w +p)-6( +w +p)-6( +w +p), + + + +Figure 13. + +Eustigmaeus fani + +n. sp. +(female): (A) leg I; (B) leg II; (C) leg III; (D) leg IV. + + + + +Figure 14. + +Eustigmaeus fani + +n. sp. +(male): (A) dorsal view; (B) ventral view. + + + +genua 4( +k +)-4( +k +)-1-1, femora 6-5-3-2, trochanters 1-1-2-1, coxae 2-2-2-2. Lengths of solenidia on tarsi: +v +1 +23, +v +2 +17, +v +3 +7, +v +4 +4. + + +Male + +Length of body (excluding gnathosoma) 297, width 167. + +Dorsum + + +Dorsal ornamentation as in female but dorsal dimples indiscernible. Dorsal body setae different from those of female, subspatulate distally. Dimensions of setae as follows: +υi +5 +sce +33, +υe +37, +sci +27, +c +1 +30, +c +2 +20, +d +15 +d +2 +33, + +e +1 +27 + +, + +e +2 +30 + +, +f +1 +37, +h +1 +14, +h +2 +33. Distance between setae: +υi–υi +23, +υe–υe +75, +υi–υe +40, +sci–sci +127, +υe–sci +30, +sce–sce +157, +sci–sce +37, +c +1 +–c +1 +77, +d +1 +– d +1 +90, +c +1 +–d +1 +60, +c +1 +–d +2 +47, +d +2 +– +d +2 +160, +d +1 +– +d +2 +50, +e +1 +–e +1 +67, +e +2 +–e +2 +110, +e +1 + +– +e + +2 +33, +d +1 + +– +e + +1 +53, +d +2 +–e +2 +70, +d +1 + +– +e + +2 +27, +f +1 +–f +1 +60, +e +1 +–f +1 +13, +h +1 +–h +1 +27, +h +2 +–h +2 +50, +h +1 +–h +2 +13. + + +Venter + + +As in female but ophistosoma with two pairs of aggenital setae. Pseudanal covers with three pairs setae, +ps +1, 2 +peg-like. + + +Legs + + +Leg I 250, leg II 207, leg III 187, leg IV 217. Number of setae (solenidia in parentheses) on leg segments (I–IV) as follows: tarsi 15( +v +, +v„ +)-11( +v +, +v„ +)-9( +v +, +v„ +)-9( +v +, +v„ +), tibiae 7( +w +, +w +p)- 6( +w +p)-6( +w +p)-6( +w +p), genua 4( +k +)-4( +k +)-1-1, femora 6-5-3-2, trochanters 1-1-2-1, coxae 2-2-2-2. All tarsi with solenidia +v +and +v„ +. + + +Etymology + + +This species is named in honour of Dr Qing-Hai Fan, +Fujian +Agricultural and Forestry University, +China +. + + +Remarks + + +This new species closely resembles +E. ottaυii + +Berlese, +1910 + +in that dimples on the dorsal shields are very shallow and indiscernible mid-dorsally. However, it differs from the latter species in length of the dorsal body setae, in the humeral setae +c +2 +being approximately half as long as preocular setae +υe +, and fossettes on dorsal shields indistinct. Dorsal body setae of + +Eustigmaeus fani + +have many minute spinules, but those of +E. ottaυii +have five to eight spinules. This species also resembles + +E. manapouriensis +( +Wood, 1966 +) + +, but can be easily distinguished from it by having major and minor callosities and three pairs of aggenital setae. + + + + \ No newline at end of file diff --git a/data/38/08/62/3808620CFFFDA163FE76F351FC0B051E.xml b/data/38/08/62/3808620CFFFDA163FE76F351FC0B051E.xml new file mode 100644 index 00000000000..848d31df1a6 --- /dev/null +++ b/data/38/08/62/3808620CFFFDA163FE76F351FC0B051E.xml @@ -0,0 +1,388 @@ + + + +Eustigmaeus mites from Turkey (Acari: Stigmaeidae) + + + +Author + +Sali + + + +Author + +Doğan, H + +text + + +Journal of Natural History + + +2005 + +2005-03-31 + + +39 + + +11 + + +835 +861 + + + + +http://dx.doi.org/10.1080/00222930400001558 + +journal article +10.1080/00222930400001558 +1464-5262 +4668774 + + + + + + +Eustigmaeus erzurumensis + +n. sp. + + + + + +( +Figure 11 +) + + +Type materials + + + +Holotype +female and four +paratype +females from soil and moss under + +Ostyra carpinifolia +, Köprüköy Village, I + +˙spir, +Erzurum +, + +4 August 2001 + +; +13 paratype females +from moss, +Uzunoluk Forest +, +Oltu +, +Erzurum +, + +15 June 2001 + +; two +paratype +females from moss and lichen on decayed stump, +Uzunoluk Forest +, +Oltu +, +Erzurum +, + +15 June 2001 + +. + + + +Female + + +Holotype +: length of body (excluding gnathosoma) 367, width 253. + + +Dorsum + + +Dorsal shields with almost circular dimples, each dimple consists of 9–12 irregularly scattered vacuoles, a few with four or 15 vacuoles. Surface between dimples with fine punctations. Fossettes on dorsal shields as illustrated. Propodosomal shield with four pairs of setae and one pair of eyes. Hysterosomal shield with six pairs of setae, suranal shield with two pairs of setae. Dorsal body setae short, subspatulate–spinulate. Dimensions of setae as follows: +υi +33, +υe +5 +sci +30, +sce +36, +c +1 +27, +c +2 +35, +d +1 +27, +d +2 +30, + +e +1 +30 + +, + +e +2 +33 + +, +f +1 +50, +h +15 +h +2 +40. Distance between setae: +υi–υi +43, +υe–υe +113, +υi–υe +43, +sci–sci +180, +υe–sci +43, +sce–sce +223, +sci–sce +50, +c +1 +–c +1 +97, +d +1 +–d +1 +90, +c +1 +–d +2 +77, +c +1 +–d +1 +60, +d +2 +– +d +2 +247, +d +1 +– +d +25 +e +1 +–e +1 +77, +e +2 +–e +2 +197, +e +1 +–e +25 +d +1 +–e +2 +67, +d +1 +–e +15 +d +2 +–e +2 +73, +f +1 +–f +1 +107, +e +1 +–f +1 +43, +e +2 +–f +1 +80, +h +1 +–h +1 +47, +h +2 +–h +2 +90, +h +1 +–h +2 +20. + + + +Figure 11. + +Eustigmaeus erzurumensis + +n. sp. +(female): (A) dorsal view; (B) ventral view. + + + +Venter + + +Humeral shields with dimples bearing vacuoles; setae +c +2 +dissimilar to other dorsals, slender, acute, with short spinules. Humeral regions without callosities. Coxisternal shields completely fused, reticulate with punctations, posterior coxisternal shield with large circle medially, with punctations and striations. Coxisternal shields bearing +1a +, +3a +and +4a +. Surface on coxae punctate and faintly reticulate. Aggenital shield with dimples and vacuoles; with three pairs of setae, +ag +1 +and +ag +3 +subequal in length, +ag +2 +slightly shorter than others. Pseudanal covers bearing three pairs of setae, subequal in length, +ps +1 +thicker than others, with spinules. Humeral, aggenital and suranal shields with similar patterns. + + +Legs + + +Leg I 210, leg II 183, leg III 157, leg IV 200. Number of setae (solenidia in parentheses) on leg segments (I–IV) as follows: tarsi 14( +v +)-10( +v +)-8( +v +)-7, tibiae 7( +w +, +w +p)-6( +w +p)-6( +w +p)-6( +w +p), + + +genua 4( +k +)-4( +k +)-1-1, femora 6-4-3-2, trochanters 1-1-2-1, coxae 2-2-2-2. Lengths of solenidia on tarsi: +v +1 +20, +v +2 +13, +v +3 +7, +v +4 +absent. Femur II with four setae. + + +Male + +Unknown. + +Etymology + + + +The species name + +erzurumensis + +refers to the +type +locality, +Erzurum + +. + + +Remarks + + +This species resembles + +E. anauniensis +( +Canestrini, 1889 +) + +and + +E. kentingensis +Tseng, 1982 + +, but differs from them in the dorsal ornamentation and the shape of setae +c +2 +. + + + + \ No newline at end of file diff --git a/data/38/08/62/3808620CFFFFA165FE75F3A9FD35035B.xml b/data/38/08/62/3808620CFFFFA165FE75F3A9FD35035B.xml new file mode 100644 index 00000000000..cd9c03470f4 --- /dev/null +++ b/data/38/08/62/3808620CFFFFA165FE75F3A9FD35035B.xml @@ -0,0 +1,357 @@ + + + +Eustigmaeus mites from Turkey (Acari: Stigmaeidae) + + + +Author + +Sali + + + +Author + +Doğan, H + +text + + +Journal of Natural History + + +2005 + +2005-03-31 + + +39 + + +11 + + +835 +861 + + + + +http://dx.doi.org/10.1080/00222930400001558 + +journal article +10.1080/00222930400001558 +1464-5262 +4668774 + + + + + + +Eustigmaeus erzincanensis + +n. sp. + + + + + +( +Figure 10 +) + + +Type materials + + + +Holotype +female and three +paratype +females from moss, +Ahmediye +, +Erzincan +, + +28 April 2001 + +. + + + +Female + + +Holotype +: length of body (excluding gnathosoma) 447, width 310. + + +Dorsum + + +Dorsal shields covered with circular dimples bearing vacuoles, some vacuoles more distinct than others, faint punctations between dimples. Fossettes on dorsal shown as +Figure 10A +. Propodosomal shield with four pairs of setae and one pair of eyes. Hysterosomal shield with six pairs of setae, suranal shield with two pairs of setae. Dorsal body setae smooth, swordshaped, with axial core and thin hyaline sheath, setae +f +1 +with a few fine and short spinules, setae +h +1 +similar to other dorsal setae but without core and with spinules, setae +h +2 +unsheathed, very short and spinulate. Dimensions of setae as follows: +υi +72, +υe +100, +sci +23, +sce +87, +c +1 +83, +c +2 +39, +d +1 +97, +d +2 +83, +e +1 +113, +e +2 +100, +f +1 +93, +h +1 +57, +h +2 +43. Setae +sci +shorter than +c +2 +. Distance between setae: +υi–υi +32, +υe–υe +133, +υi–υe +54, +sci–sci +230, +υe–sci +63, +sce–sce +263, +sci–sce +40, +c +1 +–c +1 +110, +d +1 +–d +1 +87, +c +1 +–d +2 +117, +c +1 +–d +1 +93, +d +2 +– +d +2 +273, +d +1 +– +d +2 +100, +e +1 +–e +1 +153, +e +2 +–e +2 +250, +e +1 +–e +2 +67, +d +1 +–e +1 +130, +d +1 +–e +2 +107, +d +2 +–e +2 +90, +f +1 +– +f +1 +112, +e +1 +– +f +1 +40, +e +2 +– +f +1 +113, +h +1 +–h +1 +43, +h +2 +–h +2 +104, +h +1 +–h +2 +33. + + + +Figure 10. + +Eustigmaeus erzincanensis + +n. sp. +(female): (A) dorsal view; (B) ventral view; (C) dorsal ornamentation; (D) lateral view. + + + +Venter + + +Setae +c +2 +placed on triangular dimpled humeral shields. Humeral regions with major callosities, covered with pores, not conjunct to margins of dorsal shields, minor callosities absent. Surface on coxae faintly reticulate and densely punctate. Coxisternal shields completely divided with polygonal dimples and bearing +1a +, +3a +and +4a +. Aggenital shield with polygonal dimples, two pairs of subequal setae. Pseudanal covers with three pairs of subequal setae. Humeral and suranal shields with similar patterns as that of dorsum. + + +Legs + + +Leg I 333, leg II 263, leg III 260, leg IV 327. Number of setae (solenidia in parentheses) on leg segments (I–IV) as follows: tarsi 14( +v +)-10( +v +)-8( +v +)-8( +v +), tibiae 7( +w +, +w +p)-6( +w +p)-6( +w +p)- 6( +w +p), genua 4( +k +)-4( +k +)-1-1, femora 6-5-3-2, trochanters 1-1-2-1, coxae 2-2-2-2. Lengths of solenidia on tarsi: +v +1 +28, +v +2 +18, +v +35 +v +4 +6. + + +Etymology + + + +The new species name + +erzincanensis + +refers to the +type +locality, +Erzincan + +. + + +Remarks + + +The new species is similar to + +E. erciyesiensis +Doğan, Ayyıldız and Fan, 2003 + +. However, it can be distinguished from the latter by having setae +4a +on the metasternal shield and postocular setae +sci +shorter than humeral setae +c +2 +. + + + + \ No newline at end of file diff --git a/data/38/08/8D/38088D004F7D55FD8F637E6FF5900E8B.xml b/data/38/08/8D/38088D004F7D55FD8F637E6FF5900E8B.xml new file mode 100644 index 00000000000..22b00149169 --- /dev/null +++ b/data/38/08/8D/38088D004F7D55FD8F637E6FF5900E8B.xml @@ -0,0 +1,199 @@ + + + +A taxonomic monograph of the liphistiid spider genus Heptathela, endemic to Japanese islands + + + +Author + +Xu, Xin + + + +Author + +Ono, Hirotsugu + + + +Author + +Kuntner, Matjaz + + + +Author + +Liu, Fengxiang + + + +Author + +Li, Daiqin + +text + + +ZooKeys + + +2019 + +888 + + +1 +50 + + + + +http://dx.doi.org/10.3897/zookeys.888.34494 + +journal article +http://dx.doi.org/10.3897/zookeys.888.34494 +1313-2970-888-1 +B995C05697EC41A49012B58F9D3AFDC1 +F8810409F4DA5A43BF94417F5D40DECE + + + + +Heptathela crypta +sp. nov. +Figs 22 +, +23 + + + +Type material. + +Holotype +: JAPAN · ♂; Okinawa-ken, Nago-shi, Haneiji-Dam, Taira; +26.59N +, +128.03E +; alt. 100 m; 18 December 2012; D. Li, F.X. Liu and X. Xu leg.; XUX-2012-328. + + +Paratypes +: JAPAN · 1 ♂, 3 ♀♀; same data as for holotype; XUX-2012-324, 326, 327, 333A · 2 ♂♂, 4 ♀♀; Okinawa Prefecture, Nago-shi, County Road 18 south, Nago/Yofuke; +26.57N +, +128.01E +; alt. 150 m; 24 December 2012; D. Li, F.X. Liu and X. Xu leg.; XUX-2012-457 to 462 · 3 ♀♀; Okinawa Prefecture, Nago-shi, Mt. Nago-dake; +26.58N +, +128.01E +; alt. 220 m; 06 May 2014; D. Li and B. Wu leg.; XUX-2014-027 to 027B. + + + +Diagnosis. + +Males and females of + +H. crypta + +sp. nov. cannot be distinguished morphologically from + +H. unten + +sp. nov. ( + +Figs 22 +A-K + +, + +23 +A-L + +), but can be diagnosed from + +H. unten + +sp. nov. by the following unique nucleotide substitutions in the standard DNA barcode alignment: C (26), A (32), C (50), T (60), T (110), G (153), T (194), C (197), T (269), C (281), T (284), C (338), A (341), T (357), C (416), T (428), C (458), A (482), T (488), G (551), T (581), T (635), G (638), G (641), C (644), C (656), as well as from all other Okinawa group + +Heptathela + +species by the following unique nucleotide substitutions in the standard DNA barcode alignment: C (26), T (110), G (551), C (656). + + + +Description. + +Male +(Holotype). Carapace and opisthosoma description see + +H. unten + +sp. nov.; cheliceral groove with nine denticles of variable size; seven spinnerets. Measurements: BL 7.88, CL 4.01, CW 3.51, OL 4.23, OW 3.18; ALE> PLE> PME> AME; leg I 10.15 (3.60 + 1.50 + 2.38 + 1.00 + 1.67), leg II 13.08 (3.48 + 1.58 + 2.49 + 3.53 + 2.00), leg III 14.27 (3.38 + 1.55 + 2.65 + 4.30 + 2.39), leg IV 18.19 (4.45 + 1.63 + 3.50 + 5.50 + 3.11). + + + +Palp +. + +Prolateral side of paracymbium unpigmented and unsclerotised, numerous setae and spines at the tip of paracymbium ( + +Fig. 22 +I-K + +). Contrategulum margin incurved nearly in the middle, and the contrategulum divided into proximally serrated and distally smooth ( +Fig. 22E, F, I, J +). Tegulum with wide dorsal extension of terminal apophysis ( +Fig. 22G, H, J +), blunt terminal and small marginal apophysis ( +Fig. 22H, I +). Conductor sclerotised and ovate, prolateral conductor with one or two shallow folds, and with a serrated margin ( +Fig. 22F, G, K +). Embolus sclerotised, with a wide opening, the distal margin slightly sclerotised, and with a saddle-shaped margin in the retrolateral view ( +Fig. 22F, G, K +). + + +Females +( +N += 10). Carapace and opisthosoma description see + +H. unten + +sp. nov.; chelicerae with promargin of cheliceral groove with 13-14 pronounced denticles of variable size; seven spinnerets. Measurements: BL 8.35-16.50, CL 4.07-5.10, CW 3.30-4.80, OL 4.70-6.80, OW 3.00-5.20; ALE> PLE> PME> AME; palp 7.70 (2.87 + 1.13 + 1.68 + 2.02), leg I 9.57 (3.07 + 1.70 + 1.70 + 1.98 + 1.12), leg II 9.64 (2.95 + 1.68 + 1.61 + 2.08 + 1.32), leg III 9.60 (2.68 + 1.69 + 1.50 + 2.30 + 1.43), leg IV 14.21 (4.00 + 1.92 + 2.55 + 3.83 + 1.91). + + + +Female genitalia +. + +A pair of depressions on the ventro-lateral part of genital atrium indistinct ( + +Fig. 23F, +J-L + +). Paired receptacular clusters along the anterior margin of bursa copulatrix, divided into two parts, the inners similar or smaller than the laterals, paired receptacular clusters tuberculate, without genital stalks ( + +Fig. 23C, +G-L + +). + + + +Etymology. +The species epithet, a noun in apposition, refers to the cryptic nature of this species discovery. + + +Distribution. + +The species is endemic to the Japanese island Okinawajima ( +Fig. 1C +). + + + + \ No newline at end of file diff --git a/data/38/08/EF/3808EF9C1068F0AAFA41226B857AAA25.xml b/data/38/08/EF/3808EF9C1068F0AAFA41226B857AAA25.xml new file mode 100644 index 00000000000..caf087da6fa --- /dev/null +++ b/data/38/08/EF/3808EF9C1068F0AAFA41226B857AAA25.xml @@ -0,0 +1,47 @@ + + + +Formicides de l'Antille St. Vincent. Récoltées par Mons. H. H. Smith. + + + +Author + +Forel, A. + +text + + +Transactions of the Entomological Society of London + + +1893 + +1893 + + +333 +418 + + + + +http://research.amnh.org/entomology/social_insects/ants/publications/3948/3948.pdf + +journal article +3948 +5E6A481F-664E-428C-A636-08D4BD5A1EF0 + + + + +Genre +Cremastogaster +, Lund. + + + +Observed at the southern end of the island; thickets along the seashore, or near it. In this region the ants were very numerous on the ground, tree-trunks, and foliage. The females, generally two to four or five together, and attended by many workers, were found in crevices under the outer bark of Manchioneal and Landbox trees; each little nest was two or three inches long, and perhaps an inch broad, but many were on the same tree, and perhaps formed part of the same great colony. The females are very sluggish, and when the nest is uncovered generally cling to the bark of the tree by their jaws; the workers are active and pugnacious. There were many larvae in the nests, but I could find no males. Apparently the passages of the formicarium are short, and confined to the outer bark of the tree. + + + \ No newline at end of file diff --git a/data/38/09/80/380980836CE0D8B5A97846A9CBFB819A.xml b/data/38/09/80/380980836CE0D8B5A97846A9CBFB819A.xml new file mode 100644 index 00000000000..535c1f5a91a --- /dev/null +++ b/data/38/09/80/380980836CE0D8B5A97846A9CBFB819A.xml @@ -0,0 +1,67 @@ + + + +Additional contributions to taxonomy, nomenclature and biogeography of the Turkish Crataegus (Rosaceae) taxa + + + +Author + +Doenmez, Ali A. + + + +Author + +Oezderin, Sevgin + +text + + +PhytoKeys + + +2019 + +122 + + +1 +13 + + + + +http://dx.doi.org/10.3897/phytokeys.122.33002 + +journal article +http://dx.doi.org/10.3897/phytokeys.122.33002 +1314-2003-122-1 +FFB3FFE0FE64FFD1FFAC67782443356D +3227680 + + + + + +Crataegus azarolus L. var. dentata (Browicz) +Doenmez + +comb. nov. + + + +Basionym. + +Crataegus aronia L. var. dentata +Browicz, Notes Roy. Bot. Gard. Edinburgh 31: 324. 1972. TYPE [Turkey] +Mugla +: Marmaris, +Bayir +, 15 iv 1965, +P.H.Davis +41136 (holotype: E!; isotype: K!). + + + + \ No newline at end of file diff --git a/data/38/09/A3/3809A3436E04FFFDFDCEFCE8FD12FD9E.xml b/data/38/09/A3/3809A3436E04FFFDFDCEFCE8FD12FD9E.xml new file mode 100644 index 00000000000..873c5216c60 --- /dev/null +++ b/data/38/09/A3/3809A3436E04FFFDFDCEFCE8FD12FD9E.xml @@ -0,0 +1,254 @@ + + + +Cladistic analysis and description of a new species of the Brazilian genus Atlantodesmus Hoffman, 2000 (Diplopoda: Polydesmida: Chelodesmidae) + + + +Author + +Bouzan, Rodrigo Salvador + + + +Author + +Iniesta, Luiz Felipe Moretti + + + +Author + +Brescovit, Antonio Domingos + +text + + +European Journal of Taxonomy + + +2019 + +2019-07-19 + + +538 + + +1 +17 + + + +journal article +26147 +10.5852/ejt.2019.538 +970b91ef-477c-47a6-bdb0-a1b6c09de383 +3346493 +92D114FF-94FC-49A0-A83A-08B4E5BF1B3E + + + + + + +Atlantodesmus sierwaldae + +sp. nov. + + + + +urn:lsid:zoobank.org:act: +499BF939-82E7-4191-AD2D-5E3B4240FF1E + + + + + +Figs 2–4C + + + + + +Diagnosis + + + +Males differ from all other species of the genus by the following features: paranota and posterior border of the metaterga whitish ( +Fig. 2A +); tip of acropodite hood-shaped, covering the solenomere only in mesal view ( +Fig. 2C, E +); prefemoral process of the gonopod without serrated margin ( +Fig. 2 +E−F). + + + + + +Etymology + + +The specific epithet is a patronym in honor of Dr. Petra Sierwald, for her friendship and outstanding contributions to our knowledge concerning millipedes. + + + + +Material examined + + + + +Holotype + + + + +BRAZIL +• + +adult; +Minas Gerais +, +Paracatu +; +17°14′41.6″ S +, +46°50′38.0″ W +; +K. Lenko +leg.; +IBSP 180 +. + + + + + + +Description + + + + +Male ( +holotype +) + + + +MEASUREMENTS. Total length: +47.6 mm +. Width (body ring 5): +7.2 mm +. Collum length +1.3 mm +, width +5.5 mm +. Antennomeres in mm (1–7): 0.8; 1.5; 1.6; 1.4; 1.3; 1.3; 0.4. Podomeres in mm (1–6): 0.9; 0.9; 2.0; 1.1; 1.1; 1.5. Tarsal claw: 0.3. Gonopod aperture: +1.1 mm +length, +1.9 mm +width. Telson +1.2 mm +. + + +COLORATION (in 70% ethanol). Head light brown with whitish labral region ( +Fig. 2A +). Antennae whitishyellow. Body brown; paranota and posterior margin of metaterga whitish. + + +BODY RINGS. Integument slightly rough; alignment of paranota curved slightly dorsad; anterior corners rounded, posterior edges acutely produced; ozopores and peritremata situated on the posterior edge of paranota ( +Fig. 4C +). Sterna without modifications. + + +LEGS. Whitish yellow and without modifications, with thin and slightly elongated setae. Gonopod aperture transversely oval; posterior edge excavated and with folds. Telson light brown with whitish apex ( +Fig. 2B +); hypocroct triangular, with two setae. + + +GONOPODS ( +Fig. 2 +C−F). Gonopod: length +2.22 mm +, width +1.79 mm +. Coxae: length +0.61 mm +, width +0.93 mm +. Telopodite: length +1.99 mm +, width +0.61 mm +. Coxae equivalent to about half the length of telopodite and prominently rounded in ectal view ( +Figs 2F +, +3C +); with two or three long setae on distal dorsal side and with two or four short setae above cannula; without a spiniform process. Cannula hookshaped ( +Cn +; +Figs 2C +, +3A +). Prefemoral region ⅓ the size of telopodite; dorsal side with folds. Prefemoral process a long and broad, smooth blade, with the terminal portion expanded, acuminate at apex ( +PfP +; +Figs 2 +C–F, 3). Conspicuous cingulum present below bases of solenomere and acropodite ( +C +; +Figs 2 +E–F, 3). Solenomere long and falciform, tapering to acuminate tip; carrying the seminal groove to apical point ( +S +; +Figs 2 +E–F, 3B–C). Acropodite long, obscuring solenomere in most of its length in ectal view; overreaching the solenomere; hood-shaped. Prefemoral process covering the solenomere in most of its length in mesal view. Acropodite process weakly sclerotized and covering the apical part of the solenomere, in ectal view and also is irregular. + + + +Fig. 2. + +Atlantodesmus sierwaldae + +sp. nov. +, holotype, ♂ (IBSP 180). +A +. Anterior region in dorsal view. +B +. Posterior region in dorsal view. +C–F +. Left gonopod. +C +. Mesal view. +D +. Ventral view. +E +. Ectal view. +F +. Detail of the distal portion in ectal view. Scale bars: A–B = 2 mm; C–D = 250 µm. E–F = 500 µm. + + + +Female + +Unknown. + + + + +Distribution + + + +The species is known only from the +type +locality. + + + + \ No newline at end of file diff --git a/data/38/09/A3/3809A3436E06FFF3FDBFF8FDFA9BFCD7.xml b/data/38/09/A3/3809A3436E06FFF3FDBFF8FDFA9BFCD7.xml new file mode 100644 index 00000000000..20a1c7e5063 --- /dev/null +++ b/data/38/09/A3/3809A3436E06FFF3FDBFF8FDFA9BFCD7.xml @@ -0,0 +1,303 @@ + + + +Cladistic analysis and description of a new species of the Brazilian genus Atlantodesmus Hoffman, 2000 (Diplopoda: Polydesmida: Chelodesmidae) + + + +Author + +Bouzan, Rodrigo Salvador + + + +Author + +Iniesta, Luiz Felipe Moretti + + + +Author + +Brescovit, Antonio Domingos + +text + + +European Journal of Taxonomy + + +2019 + +2019-07-19 + + +538 + + +1 +17 + + + +journal article +26147 +10.5852/ejt.2019.538 +970b91ef-477c-47a6-bdb0-a1b6c09de383 +3346493 +92D114FF-94FC-49A0-A83A-08B4E5BF1B3E + + + + + +Genus + +Atlantodesmus +Hoffman, 2000 + + + + + + + +Atlantodesmus +Hoffman, 2000: 102 + +. +Type +species: + +Leptodesmus eimeri +Attems, 1898 + +, by original designation. + + + + +Iemanja +Hoffman, 2000: 106 + +. +Type +species: + +I. teresa +Hoffman, 2000 + +, by original designation. Synonymized by + + +Bouzan +et al +. 2017: 271 + + +. + + + + + + +Diagnosis + + + +Modified from + +Bouzan +et al. +(2017) + +: males of + +Atlantodesmus + +differ from other chelodesmid genera by the combination of the following characters: absence of ventral projections on the sternites (except + +A. itapurensis + +and + +A. teresa +, + +which have a pair of projections on the fourth sternite; +Fig. 5C +); presence of folds on the dorsal edge of the prefemoral region of the gonopod ( +Fig. 6B +), except + +A. pickeli + +; presence of a cingulum ( +Fig. 2 +E−F); acropodite branching, forming a long, thin, falciform solenomere, and a large acropodite process with a broadened apical region overreaching the tip of the solenomere ( +Fig. 2 +C−F). + + + + + +Distribution + + + +Occurring in the Atlantic rain forest (states of +Paraná +, +Santa Catarina +, +São Paulo +, +Minas Gerais +, +Espírito Santo +and +Bahia +) and in the Cerrado (states of +São Paulo +, +Mato Grosso do Sul +and +Minas Gerais +) areas of +Brazil +. See map in + +Bouzan +et al. +(2017) + +. + + + + + +Composition + + + +Six species: + +Atlantodesmus eimeri +( +Attems, 1898 +) + +, + +A. itapurensis +(Schubart, 1943) + +, + +A. pickeli +(Schubart, 1946) + +, + +A. pintoi +(Schubart, 1946) + +, + +A. teresa +(Hoffman, 2000) + +and + +A. sierwaldae + +sp. nov. + + + + +Fig. 1. +Strict consensus of the two most parsimonious trees obtained with implied weighting of the characters (k = 3) (length = 58 steps; total fit = 23.150; CI = 0.64; RI = 0.64). Black circles correspond to unique transformations and white circles to homoplastic transformations. Values below branches refer to the GC values (Symmetric Resampling) and relative Bremer support. Only unambiguous changes are shown in this topology. + + + + + + +Key to the males of + +Atlantodesmus + + + + + + + +1. Body coloration concolorous to paranota edge ................................................................................ 2 – Coloration at paranota edge lighter ................................................................................................... 3 + + + + + +2. Tubercles present on dorsal surface of metazonites ................................... + +A. eimeri +( +Attems, 1898 +) + +– Tubercles absent on dorsal surface of metazonites ................................... + +A. teresa +(Hoffman, 2000) + + + + + + + +3. Median stripe on metazonite present ........................................................ + +A. pintoi +(Schubart, 1946) + +– Median stripe on metazonite absent ................................................................................................. 4 + + + + + + +4. Prefemoral process serrated distally ................................................................................................. 5 – Prefemoral process unserrated distally ............................................................ + +A. sierwaldae + +sp. nov. + + + + + + +5. Prefemoral process densely serrated distally ........................................... + +A. pickeli +(Schubart, 1946) + +– Prefemoral process slightly serrated distally .................................... + +A. itapurensis +(Schubart, 1943) + + + + + + + + \ No newline at end of file diff --git a/data/38/09/A3/3809A3436E0CFFFBFD3BFA8DFDE2FA7F.xml b/data/38/09/A3/3809A3436E0CFFFBFD3BFA8DFDE2FA7F.xml new file mode 100644 index 00000000000..1d1fcb88bc5 --- /dev/null +++ b/data/38/09/A3/3809A3436E0CFFFBFD3BFA8DFDE2FA7F.xml @@ -0,0 +1,90 @@ + + + +Cladistic analysis and description of a new species of the Brazilian genus Atlantodesmus Hoffman, 2000 (Diplopoda: Polydesmida: Chelodesmidae) + + + +Author + +Bouzan, Rodrigo Salvador + + + +Author + +Iniesta, Luiz Felipe Moretti + + + +Author + +Brescovit, Antonio Domingos + +text + + +European Journal of Taxonomy + + +2019 + +2019-07-19 + + +538 + + +1 +17 + + + +journal article +26147 +10.5852/ejt.2019.538 +970b91ef-477c-47a6-bdb0-a1b6c09de383 +3346493 +92D114FF-94FC-49A0-A83A-08B4E5BF1B3E + + + + + + +Leiodesmus + +sp. + + + + + + +BRAZIL +• +1 ♂ +; +Mato Grosso do Sul +, +Miranda +, +Fazenda Cayman +; +20°14′27″ S +, +56°22′42″ W +; + +Oct. 1992 + +; +A. Eterovic +coll.; +IBSP1080 + +. + + + + \ No newline at end of file diff --git a/data/38/09/A3/3809A3436E0CFFFBFD92FD00FD95FCF0.xml b/data/38/09/A3/3809A3436E0CFFFBFD92FD00FD95FCF0.xml new file mode 100644 index 00000000000..8d6d57a4e7c --- /dev/null +++ b/data/38/09/A3/3809A3436E0CFFFBFD92FD00FD95FCF0.xml @@ -0,0 +1,92 @@ + + + +Cladistic analysis and description of a new species of the Brazilian genus Atlantodesmus Hoffman, 2000 (Diplopoda: Polydesmida: Chelodesmidae) + + + +Author + +Bouzan, Rodrigo Salvador + + + +Author + +Iniesta, Luiz Felipe Moretti + + + +Author + +Brescovit, Antonio Domingos + +text + + +European Journal of Taxonomy + + +2019 + +2019-07-19 + + +538 + + +1 +17 + + + +journal article +26147 +10.5852/ejt.2019.538 +970b91ef-477c-47a6-bdb0-a1b6c09de383 +3346493 +92D114FF-94FC-49A0-A83A-08B4E5BF1B3E + + + + + + +Macrocoxodesmus marcusi +Schubart, 1947 + + + + + + + +BRAZIL +• +1 ♂ +; +Minas Gerais +, +Manhuaçu +, +Rio Matipó +, +Fazenda Floresta +; +20°15′30″ S +, +42°02′01″ W +; + +Dec. 1919 + +; +R. Fonseca +coll.; +MZUSP + +. + + + + \ No newline at end of file diff --git a/data/38/09/A3/3809A3436E0CFFFBFD96F969FBA9F898.xml b/data/38/09/A3/3809A3436E0CFFFBFD96F969FBA9F898.xml new file mode 100644 index 00000000000..b90a045da5a --- /dev/null +++ b/data/38/09/A3/3809A3436E0CFFFBFD96F969FBA9F898.xml @@ -0,0 +1,92 @@ + + + +Cladistic analysis and description of a new species of the Brazilian genus Atlantodesmus Hoffman, 2000 (Diplopoda: Polydesmida: Chelodesmidae) + + + +Author + +Bouzan, Rodrigo Salvador + + + +Author + +Iniesta, Luiz Felipe Moretti + + + +Author + +Brescovit, Antonio Domingos + +text + + +European Journal of Taxonomy + + +2019 + +2019-07-19 + + +538 + + +1 +17 + + + +journal article +26147 +10.5852/ejt.2019.538 +970b91ef-477c-47a6-bdb0-a1b6c09de383 +3346493 +92D114FF-94FC-49A0-A83A-08B4E5BF1B3E + + + + + + +Atlantodesmus itapurensis +(Schubart, 1943) + + + + + + + +BRAZIL +• +1 ♂ +; +São Paulo +, +Assis +, +Estação Ecológica de Assis +; 50°41′88″ W, 22°66′04″ S; + +25–30 Nov. 2002 + +; +Equipe Biota +coll.; +IBSP 2976 + +• + +1 ♀ +; same collection data; +IBSP 2981 + +. + + + + \ No newline at end of file diff --git a/data/38/09/A3/3809A3436E0CFFFBFDBFFA52FB33F97E.xml b/data/38/09/A3/3809A3436E0CFFFBFDBFFA52FB33F97E.xml new file mode 100644 index 00000000000..41652c8b450 --- /dev/null +++ b/data/38/09/A3/3809A3436E0CFFFBFDBFFA52FB33F97E.xml @@ -0,0 +1,112 @@ + + + +Cladistic analysis and description of a new species of the Brazilian genus Atlantodesmus Hoffman, 2000 (Diplopoda: Polydesmida: Chelodesmidae) + + + +Author + +Bouzan, Rodrigo Salvador + + + +Author + +Iniesta, Luiz Felipe Moretti + + + +Author + +Brescovit, Antonio Domingos + +text + + +European Journal of Taxonomy + + +2019 + +2019-07-19 + + +538 + + +1 +17 + + + +journal article +26147 +10.5852/ejt.2019.538 +970b91ef-477c-47a6-bdb0-a1b6c09de383 +3346493 +92D114FF-94FC-49A0-A83A-08B4E5BF1B3E + + + + + + +Atlantodesmus eimeri +(Attems, 1898) + + + + + + + +BRAZIL +• +3 ♂♂ +, +1 ♀ +; +Santa Catarina +, +Blumenau +, +Nova Rússia +; +49°07′17″ W +, +26°91′65″ S +; + +20 Feb. 2013 + +; +R.P. Indicatti +and +B. Gambaré +coll.; +IBSP 4367 +• + + +1 ♀ +; +Paulo Lopes, Parque Estadual da Serra do Tabuleiro +; +48°80′35″ W +, +27°92′22″ S +; + +10–20 Jan. 2003 + +; +Equipe Biota +coll.; +IBSP 2317 +. + + + + + \ No newline at end of file diff --git a/data/38/09/A3/3809A3436E0CFFFBFE5CFE49FD9FFD56.xml b/data/38/09/A3/3809A3436E0CFFFBFE5CFE49FD9FFD56.xml new file mode 100644 index 00000000000..41abf7e520a --- /dev/null +++ b/data/38/09/A3/3809A3436E0CFFFBFE5CFE49FD9FFD56.xml @@ -0,0 +1,104 @@ + + + +Cladistic analysis and description of a new species of the Brazilian genus Atlantodesmus Hoffman, 2000 (Diplopoda: Polydesmida: Chelodesmidae) + + + +Author + +Bouzan, Rodrigo Salvador + + + +Author + +Iniesta, Luiz Felipe Moretti + + + +Author + +Brescovit, Antonio Domingos + +text + + +European Journal of Taxonomy + + +2019 + +2019-07-19 + + +538 + + +1 +17 + + + +journal article +26147 +10.5852/ejt.2019.538 +970b91ef-477c-47a6-bdb0-a1b6c09de383 +3346493 +92D114FF-94FC-49A0-A83A-08B4E5BF1B3E + + + + + +Brasilodesmus paulistus + + +paulistus +(Brölemann, 1902) + + + + + + +BRAZIL +• +1 ♂ +; +São Paulo +, +Peruíbe +, +Estação Ecológica Juréia/Itatins +; +24°16′38″ S +, +47°00′44″ W +; + +5 Mar. 1994 + +; +A. Eterovic +coll.; +IBSP 1130 + +• + +1 ♀ +; same collection data as for preceding; + +Dec. 1998 + +; +A.D. Brescovit +et al. +coll.; +IBSP 981 +. + + + + + \ No newline at end of file diff --git a/data/38/09/A3/3809A3436E0CFFFBFE68FC2BFC8DFBF8.xml b/data/38/09/A3/3809A3436E0CFFFBFE68FC2BFC8DFBF8.xml new file mode 100644 index 00000000000..e81984f86bc --- /dev/null +++ b/data/38/09/A3/3809A3436E0CFFFBFE68FC2BFC8DFBF8.xml @@ -0,0 +1,107 @@ + + + +Cladistic analysis and description of a new species of the Brazilian genus Atlantodesmus Hoffman, 2000 (Diplopoda: Polydesmida: Chelodesmidae) + + + +Author + +Bouzan, Rodrigo Salvador + + + +Author + +Iniesta, Luiz Felipe Moretti + + + +Author + +Brescovit, Antonio Domingos + +text + + +European Journal of Taxonomy + + +2019 + +2019-07-19 + + +538 + + +1 +17 + + + +journal article +26147 +10.5852/ejt.2019.538 +970b91ef-477c-47a6-bdb0-a1b6c09de383 +3346493 +92D114FF-94FC-49A0-A83A-08B4E5BF1B3E + + + + + +Arthrosolaenomeris pantanalensis +Schubart, 1943 + + + + + + +BRAZIL +• +1 ♂ +; +Mato Grosso +, +São Luiz de Cáceres +(now Cáceres); +16°04′15″ S +, +57°40′44″ W +; + +Feb. 1940 + +; +Passarelli +coll.; +MZUSP 1085 + +• + +1 ♀ +; +Porto Estrela, E.E. Serra das Araras +; +15°19′28″ S +, +57°13′39″ W +; + +12 Nov. 2017 + +; +T.F. Conceição +coll.; + +CZUFMT +MYR + +847. + + + + + \ No newline at end of file diff --git a/data/38/09/A3/3809A3436E0CFFFBFE71FBD3FDFAFB25.xml b/data/38/09/A3/3809A3436E0CFFFBFE71FBD3FDFAFB25.xml new file mode 100644 index 00000000000..50a0000087b --- /dev/null +++ b/data/38/09/A3/3809A3436E0CFFFBFE71FBD3FDFAFB25.xml @@ -0,0 +1,91 @@ + + + +Cladistic analysis and description of a new species of the Brazilian genus Atlantodesmus Hoffman, 2000 (Diplopoda: Polydesmida: Chelodesmidae) + + + +Author + +Bouzan, Rodrigo Salvador + + + +Author + +Iniesta, Luiz Felipe Moretti + + + +Author + +Brescovit, Antonio Domingos + +text + + +European Journal of Taxonomy + + +2019 + +2019-07-19 + + +538 + + +1 +17 + + + +journal article +26147 +10.5852/ejt.2019.538 +970b91ef-477c-47a6-bdb0-a1b6c09de383 +3346493 +92D114FF-94FC-49A0-A83A-08B4E5BF1B3E + + + + + +Plectrogonodesmus gounellei +(Brölemann, 1903) + + + + + + +BRAZIL +• +1 ♂ +, +1 ♀ +; +Bahia +, +Guanambi +, +Aeroporto +; +14°13′25″ S +, +42°46′52″ W +; + +14 Dec. 2007 + +; +C.A.R. Souza +et al. +coll.; +IBSP 3281 + +. + + + + \ No newline at end of file diff --git a/data/38/09/A3/3809A3436E0DFFFAFDABFEA4FC61FE54.xml b/data/38/09/A3/3809A3436E0DFFFAFDABFEA4FC61FE54.xml new file mode 100644 index 00000000000..5cc65573546 --- /dev/null +++ b/data/38/09/A3/3809A3436E0DFFFAFDABFEA4FC61FE54.xml @@ -0,0 +1,92 @@ + + + +Cladistic analysis and description of a new species of the Brazilian genus Atlantodesmus Hoffman, 2000 (Diplopoda: Polydesmida: Chelodesmidae) + + + +Author + +Bouzan, Rodrigo Salvador + + + +Author + +Iniesta, Luiz Felipe Moretti + + + +Author + +Brescovit, Antonio Domingos + +text + + +European Journal of Taxonomy + + +2019 + +2019-07-19 + + +538 + + +1 +17 + + + +journal article +26147 +10.5852/ejt.2019.538 +970b91ef-477c-47a6-bdb0-a1b6c09de383 +3346493 +92D114FF-94FC-49A0-A83A-08B4E5BF1B3E + + + + + + +Atlantodesmus pickeli +(Schubart, 1946) + + + + + + + +BRAZIL +• +1 ♂ +; +São Paulo +, +São Paulo +, +Jardim São Bento +; +46°38′0″ W +, +23°33′0″ S +; 1939; +Dom B.J. Pickel +coll.; +IBSP 29 + +• + +1 ♀ +; same collection data; +IBSP 4433 + +. + + + + \ No newline at end of file diff --git a/data/38/09/A3/3809A3436E0DFFFAFDB6FE1EFDD3FDEE.xml b/data/38/09/A3/3809A3436E0DFFFAFDB6FE1EFDD3FDEE.xml new file mode 100644 index 00000000000..dc06e4969de --- /dev/null +++ b/data/38/09/A3/3809A3436E0DFFFAFDB6FE1EFDD3FDEE.xml @@ -0,0 +1,90 @@ + + + +Cladistic analysis and description of a new species of the Brazilian genus Atlantodesmus Hoffman, 2000 (Diplopoda: Polydesmida: Chelodesmidae) + + + +Author + +Bouzan, Rodrigo Salvador + + + +Author + +Iniesta, Luiz Felipe Moretti + + + +Author + +Brescovit, Antonio Domingos + +text + + +European Journal of Taxonomy + + +2019 + +2019-07-19 + + +538 + + +1 +17 + + + +journal article +26147 +10.5852/ejt.2019.538 +970b91ef-477c-47a6-bdb0-a1b6c09de383 +3346493 +92D114FF-94FC-49A0-A83A-08B4E5BF1B3E + + + + + + +Atlantodesmus pintoi +(Schubart, 1946) + + + + + + + +BRAZIL +• +1 ♂ +, +1 ♀ +; +Bahia +, +Una +, +Reserva Biológica de Una +; 39°02′98″ W, +15°19′54″ S +; + +Nov. 2001 + +; +A.D. Brescovit +coll.; +IBSP 1001 + +. + + + + \ No newline at end of file diff --git a/data/38/09/A3/3809A3436E0DFFFAFDB7FDF8FB08FD24.xml b/data/38/09/A3/3809A3436E0DFFFAFDB7FDF8FB08FD24.xml new file mode 100644 index 00000000000..ac201b2c2d3 --- /dev/null +++ b/data/38/09/A3/3809A3436E0DFFFAFDB7FDF8FB08FD24.xml @@ -0,0 +1,107 @@ + + + +Cladistic analysis and description of a new species of the Brazilian genus Atlantodesmus Hoffman, 2000 (Diplopoda: Polydesmida: Chelodesmidae) + + + +Author + +Bouzan, Rodrigo Salvador + + + +Author + +Iniesta, Luiz Felipe Moretti + + + +Author + +Brescovit, Antonio Domingos + +text + + +European Journal of Taxonomy + + +2019 + +2019-07-19 + + +538 + + +1 +17 + + + +journal article +26147 +10.5852/ejt.2019.538 +970b91ef-477c-47a6-bdb0-a1b6c09de383 +3346493 +92D114FF-94FC-49A0-A83A-08B4E5BF1B3E + + + + + + +Atlantodesmus teresa +(Hoffman, 2000) + + + + + + + +BRAZIL +• +1 ♀ +; +Espírito Santo +, +Linhares +, +Reserva Natural Vale do Rio Doce +; +40°06′37″ W +, 19°13′74″ S; + +09–15 Jan. 2012 + +; +J.P.P. Pena-Barbosa +et al. +coll.; +IBSP 4106 +• + + +1 ♂ +; +São Mateus Reserva Florestal do Vale do Rio Doce +; +39°85′67″ W +, +18°71′91″ S +; + +05–12 Jan. 1998 + +; +A.D. Brescovit +coll.; +IBSP 565 +. + + + + + \ No newline at end of file diff --git a/data/38/09/A3/3809A3436E0DFFFAFDCEFC8FFAD6FCA2.xml b/data/38/09/A3/3809A3436E0DFFFAFDCEFC8FFAD6FCA2.xml new file mode 100644 index 00000000000..782689bcd6d --- /dev/null +++ b/data/38/09/A3/3809A3436E0DFFFAFDCEFC8FFAD6FCA2.xml @@ -0,0 +1,84 @@ + + + +Cladistic analysis and description of a new species of the Brazilian genus Atlantodesmus Hoffman, 2000 (Diplopoda: Polydesmida: Chelodesmidae) + + + +Author + +Bouzan, Rodrigo Salvador + + + +Author + +Iniesta, Luiz Felipe Moretti + + + +Author + +Brescovit, Antonio Domingos + +text + + +European Journal of Taxonomy + + +2019 + +2019-07-19 + + +538 + + +1 +17 + + + +journal article +26147 +10.5852/ejt.2019.538 +970b91ef-477c-47a6-bdb0-a1b6c09de383 +3346493 +92D114FF-94FC-49A0-A83A-08B4E5BF1B3E + + + + + + +Atlantodesmus sierwaldae + +sp. nov. + + + + + + +BRAZIL +• +1 ♂ +; +Minas Gerais +, +Paracatu +; +17°14′41.6″ S +, +46°50′38.0″ W +; +K. Lenko +coll.; +IBSP 180 + +. + + + + \ No newline at end of file diff --git a/data/38/09/A6/3809A6018B2AE10DC9D6376E576CEE45.xml b/data/38/09/A6/3809A6018B2AE10DC9D6376E576CEE45.xml new file mode 100644 index 00000000000..7616f850de6 --- /dev/null +++ b/data/38/09/A6/3809A6018B2AE10DC9D6376E576CEE45.xml @@ -0,0 +1,51 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Phalaena glaucinalis +[ +spec. nov. +] + + + + +P. +Pyralis +recurvicornis, alis glabris glaucis: strigis duabus flavis arcuatis remotissimis. + + + + +Habitat in +Europa. + + + + \ No newline at end of file diff --git a/data/38/09/D6/3809D617BDC05189A41621845D25E680.xml b/data/38/09/D6/3809D617BDC05189A41621845D25E680.xml new file mode 100644 index 00000000000..fc3c7071aff --- /dev/null +++ b/data/38/09/D6/3809D617BDC05189A41621845D25E680.xml @@ -0,0 +1,218 @@ + + + +The first record of Tricholathys Chamberlin & Ivie, 1935 (Araneae, Dictynidae) from China, with a new combination and descriptions of seven new species + + + +Author + +Wang, Lu-Yu +https://orcid.org/0000-0002-5250-3473 +Key Laboratory of Eco-environments in Three Gorges Reservoir Region (Ministry of Education), School of Life Sciences, Southwest University, Chongqing 400715, China + + + +Author + +Peng, Xian-Jin +https://orcid.org/0000-0002-2614-3910 +College of Life Sciences, Hunan Normal University, Changsha 410081, Hunan, China + + + +Author + +Zhang, Zhi-Sheng +https://orcid.org/0000-0002-9304-1789 +Key Laboratory of Eco-environments in Three Gorges Reservoir Region (Ministry of Education), School of Life Sciences, Southwest University, Chongqing 400715, China +zhangzs327@qq.com + +text + + +ZooKeys + + +2023 + +2023-11-29 + + +1185 + + +255 +267 + + + + +http://dx.doi.org/10.3897/zookeys.1185.107005 + +journal article +http://dx.doi.org/10.3897/zookeys.1185.107005 +1313-2970-1185-255 +568A472D950D4338A7DF56C6EE473761 +DEA7C60064865535B07A16D0F5AC891D + + + + + +Tricholathys xizangensis sp. nov. (西藏毛隐蛛) + + + + +Figs 14 +, 15 +, 16 + + + +Type materials. + + +Holotype +male + +: China, Tibet, Coqen County, Meiduo Village, +30°39′19.43′′N +, +85°7′54.62′′E +, elev. 4751 m, 29 July 2020, L.Y. Wang et al, leg. (SWUC-T-DI-13-01). +Paratypes +(1 male and 5 females): 4 females (SWUC-T-DI-13-02~05), with same data as holotype; 1 male and 1 female, +Ge'gyai +County, +32°31′17.51′′N +, +82°28′47.63′′E +, elev. 4321 m, 29 July 2020, L.Y. Wang et al. leg. (SWUC-T-DI-13-06~07). + + + +Etymology. +The specific name is derived from the type locality the location of the type locality in Tibet; Xizang is a Chinese name for Tibet. + + +Diagnosis. + +This species can be distinguished from all other congeners in having the posterior arm of conductor short and with a hook-shaped end, the anterior arm of the conductor terminating at about the 9 +o'clock +position, the embolus originated at about 7:30 +o'clock +(Figs +14A, B +, +15C-E +), the copulatory ducts long, with 3 turns, and with an indistinct membranous part (Figs +14C, D +, +15F, G +). + + + +Figure 14. + +Tricholathys xizangensis + +sp. nov. +A, B +holotype male +C, D +paratype female +A +left male palp, ventral view +B +same, retrolateral view +C +Epigyne, ventral view +D +same, dorsal view. Abbreviations: AA = anterior arm of conductor; CD = copulatory duct; CO = copulatory opening; DP = digitiform process; Em = embolus; FD = fertilization duct; PA posterior arm of conductor; RTA = retrolaterial tibial apophysis; Sp spermatheca. + + + + +Figure 15. + +Tricholathys xizangensis + +sp. nov. +A, C-E +holotype male +B, F, G +paratype female +A +male habitus, dorsal view +B +Female habitus, dorsal view +C +left male palp, prolateral view +D +same, ventral view +E +same, retrolateral view +F +epigyne, ventral view +G +same, dorsal view. + + + + +Description. + +Male (holotype). +Habitus as (Fig. +15A +) total length 4.95. Total length of males 4.95-5.50. Prosoma 2.52 long, 1.90 wide; opisthosoma 2.70 long, 1.74 wide. Eye sizes and interdistances: AME 0.08, ALE 0.11, PME 0.08, PLE 0.11; AME-AME 0.08, AME-ALE 0.06, PME-PME 0.15, PME-PLE 0.12, ALE-PLE 0.04. MOA 0.25 long, anterior width 0.25, posterior width 0.31. Clypeus height 0.13. Chelicerae with 4 promarginal and 2 retromarginal teeth. Leg measurements: I 5.59 (1.63, 2.05, 1.11, 0.80); II 4.93 (1.43, 1.68, 1.07, 0.75); III 4.44 (1.34, 1.41, 0.95, 0.74); IV 5.86 (1.66, 1.96, 1.37, 0.87). + + +Palp +(Figs +14A, B +, +15C-E +). Tibia with retrolateral apophysis with broad, rounded tip. Tip of Cymbium with 3 spines. Anterior arm terminating at about 9:00 +o'clock +; posterior arm terminating in digitiform, uncinate tip. Embolus originating at about 7:30 +o'clock +position. + + +Female (paratype). +Habitus as in Fig. +15B +. Total length 4.35 (4.35-5.91 in other paratype females). Prosoma 2.26 long, 1.67 wide; opisthosoma 2.48 long, 1.53 wide. Eye sizes and interdistances: AME 0.09, ALE 0.11, PME 0.08, PLE, 0.09; AME-AME 0.09, AME-ALE 0.04, PME-PME 0.14, PME-PLE 0.12, ALE-PLE 0.06. MOA 0.27 long, anterior width 0.27, posterior width 0.31. Clypeus height 0.17. Leg measurements: I 4.88 (1.43, 1.65, 1.08, 0.72); II 4.58 (1.37, 1.52, 1.00, 0.69); III 4.08 (1.16, 1.27, 1.00, 0.65); IV 5.49 (1.49, 1.92, 1.26, 0.82). + + +Epigyne +(Figs +14C, D +, +15F, G +). Copulatory openings almost semicircular. Spermathecae small. Weakly sclerotized part indistinct; strongly sclerotized part spiral, with 3 turns. + + +Distribution. +China (Tibet) (Fig. +16 +). + + + +Figure 16. +Distribution of + +Tricholathys + +in China. + + + + + + \ No newline at end of file diff --git a/data/38/0A/7F/380A7F88706F5A2E817B21F8CBAC1F78.xml b/data/38/0A/7F/380A7F88706F5A2E817B21F8CBAC1F78.xml new file mode 100644 index 00000000000..5c6d040591b --- /dev/null +++ b/data/38/0A/7F/380A7F88706F5A2E817B21F8CBAC1F78.xml @@ -0,0 +1,523 @@ + + + +Taxonomic revision of charon -, floridanum - and muscaeforme - groups of Gryon Haliday, 1833 (Hymenoptera, Scelionidae) from Japan, with descriptions of two new species and host information + + + +Author + +Komeda, Yoto +Entomological Laboratory, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, Motooka 744, Fukuoka, 819 - 0395, Japan +kome123k123@gmail.com + + + +Author + +Mita, Toshiharu +https://orcid.org/0000-0001-8322-6045 +Entomological Laboratory, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, Motooka 744, Fukuoka, 819 - 0395, Japan + + + +Author + +Hirose, Yoshimi +Entomological Laboratory, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, Motooka 744, Fukuoka, 819 - 0395, Japan + + + +Author + +Yamagishi, Kenzo +Entomological Laboratory, Faculty of Agriculture, Kyushu University, Motooka 744, Fukuoka, 819 - 0395, Japan + +text + + +Journal of Hymenoptera Research + + +2020 + +2020-12-29 + + +80 + + +99 +135 + + + + +http://dx.doi.org/10.3897/jhr.80.56178 + +journal article +http://dx.doi.org/10.3897/jhr.80.56178 +1314-2607-80-99 +F9DF28B5BF7545F5860B3FB234679C6D +BCA40A8EFADF5E8A9E51A75C7C3C0D1C +4420570 + + + + +Gryon fulvicoxa Komeda & Mita +sp. nov. + + + + +Figs 1A +, 2A +, 3A +, 4A +, 5A, G +, 6A + + + +Diagnosis. +Frontal depression transversely costate by strong irregular carinae. Horizontal portion of occipital carina straight, short, reaching longitudinal extension line of outer margin of lateral ocelli. Legs entirely yellow. + + +Description. + +Female. +Length = 1.1-1.3 mm. + + +Color +(Figs +1A +, +2A +). +Body +mainly dark brown-black. A2-6, forecoxa brown. A1, mandibles, and legs (including mid and hind coxae) yellow. + + + +Figure 1. +Japanese + +Gryon + +spp., dorsal view +A + +G. fulvicoxa + +sp. nov., holotype +B + +G. japonicum + +C + +G. yamagishii + +D + +G. philippinense + +E + +G. shisa + +sp. nov., holotype +F + +G. pennsylvanicum + +. Scale bars: 1 mm. + + + + +Figure 2. +Japanese + +Gryon + +spp., lateral views +A + +G. fulvicoxa + +sp. nov., holotype +B + +G. japonicum + +C + +G. yamagishii + +D + +G. philippinense + +E + +G. shisa + +sp. nov., paratype +F + +G. pennsylvanicum + +. Scale bars: 1 mm. + + + + +Head +. + +FCI = 1.20-1.33; LCI = 1.48-1.64; DCI = 1.86-2.05; HW/IOS = 1.76-1.83; head about 1.3 times as wide as mesosoma. (HW/TSL = 1.25-1.34). Frons (Fig. +3A +) reticulate with setae; central carina present ventrally; frontal depression weakly developed, transversely costate by strong irregular carinae. Vertex reticulate with setae; interocellar space reticulate; hyperoccipital carina absent; POL 3.1 times as long as OOL (POL/OOL = 2.84-3.32); OOL half times as long as LOL (OOL/LOL = 0.48-0.63). Clypeus rectangular, with rounded corners. Gena coriaceous with setae; medial genal carina absent. Occiput (Fig. +4A +) transversely costate with setae; occipital carina complete; angular point of occipital carina developed; horizontal portion of occipital carina straight, short, reaching longitudinal extension line of outer margin of lateral ocelli; postoccipital carina discontinuity present; postgena weakly costate along postoccipital carina; postgenal sulcus curved toward hypostoma; postgenal bridge smooth, weakly longitudinally costate beside median sulcus. Antennae (Fig. +5A +) clavate; A1 about 3.2 times longer than radicle, as long as clava; clava with five segments; claval sensilla formula A8-12/2-2-2-2-1; claval length about 3.7 times longer than width. Mandible thin, tridentate, anterior tooth longer than other teeth. + + + +Mesosoma +. + +Cervical pronotal area granulate with dense setae; epomial carina strongly present, not reaching dorsal edge; pronotal suprahumeral sulcus foveolate, unclear mesad; lateral pronotal area smooth with transverse sparse carinae. Propleuron smooth with imbricate sculpture. Mesoscutum about 1.4 times as wide as long (TSL/ML = 1.35-1.49), with dense setae, reticulate anteriorly, longitudinally costate posteriorly; parascutal carina absent; notaulus absent. Mesoscutellum about 2.3 times as wide as long (SW/SL = 2.10-2.43) with dense setae, longitudinally costate mesad, granulate laterad. Mesopleuron smooth with transverse dense carinae above mesopleural canina, smooth with sparse setae below mesopleural canina; prespecular and mesepisternal sulci foveolate; prespecular sulcus with setae; mesopleural carina strongly present; postacetabular sulcus foveolate. Metascutellum weakly produced, longitudinally striate. Dorsal metapleural area smooth with setae dorsad; ventral metapleural area weakly rugulose with setae; anterior part of metapleural sulcus and upper paracoxal sulcus with setae. Propodeum foveolate with setae. Fore wing (Fig. +7A +), stigmal vein about 1.6 times longer than marginal vein; postmarginal vein about 3.5 times longer than marginal vein. + + + +Metasoma +. + +T1 longitudinally striate, setose laterally. S1 longitudinally striate. T2 longitudinally striate anteriorly, reticulate posteriorly, setose laterally. S2 with setae, granulate mesad, striate laterad. T3 reticulate, with setae laterad and posteriorly. S3-6 punctate with setae. T4 punctate-striate with setae. T5-6 punctate with setae. + + +Male. +Almost same as female, but antennae (Fig. +5G +) filiform; A1 yellow, A2-11 brown. + + + +Host. +Unknown. + + +Material examined. + + +Holotype + +: +Hokkaido +, +Sapporo city, Toyohira ward +, +Hitsujigaoka +. +43.008°N +, +141.415°E +; alt. + +100 m + +, + +8-15.VI.2010 + +, Kazuhiko Konishi leg. (MT) +1♀ +[ +ELKU +]. + +Paratypes +. +Same +locality as holotype + +, +1-8.VI.2010 +, Kazuhiko Konishi leg. (MT) +1♀ +[ELKU]; +8-15.VI.2010 +, Kazuhiko Konishi leg. (MT) +1♀ +[ELKU]; +22-29.VI.2010 +, Kazuhiko Konishi leg. (MT) +1♀ +[ELKU]; +6-13.VII.2010 +, Kazuhiko Konishi leg. (MT) +1♀ +[ELKU]; + +27.VII.-3.VIII.2010 +, +Kazuhiko Konishi +leg. (MT) +1♂ +[ELKU]; +1♂ +1♀ +[EUMJ]; +Tokyo +pref., +Minami-Tama dist. +, +Asakawa town +, +Mt. Takao-san + +, + +19.V.1935 +, +H. Ise +leg. +1♀ +[NIAES]; +Nagano +pref., +Ueda +city, + +Sugadaira-Kogen + +, +Tsukuba University + +, + +26. VII-1.VIII.2015 +. +So Shimizu +leg. (MT) +1♀ +[ELKU]; +Gifu +pref., +Kani +city, +Katabira + +, +10-16.IV.2004 +, Kenzo Yamagishi leg. (MT) +1♀ +[ELMU]; +26.VI.-2.VII.2004 +. Kenzo Yamagishi leg., +1♀ +[ELMU]; + +24-30.VII.2004 +. +Kenzo Yamagishi +leg., +2♀ +[ELMU]; +Tottori +pref., +Saihaku dist. +, +Daisen town +, +Mt. Daisen + +, + +25.VIII.1970 +. +1♂ +1♀ +[ELKU]; +Fukuoka +pref., +Fukuoka +city, +Sawara +ward, +Mt. Sefuri-san + +, + +1.VIII.1992 +, +Yoshimitsu Higashiura +leg. +1♀ +[ELKU]; +Tagawa dist. +, +Soeda town +, +Mt. Hiko-san + +. +12.IX.1968 +, (MT) +1♀ +[ELKU]; +11.VII.1969 +. Kenkichi Kanmiya leg. +3♂ +3♀ +[ELKU]; + +12-19.V.2008 +, +Toshiharu Mita +and +Sinsuke Sato +leg. (MT) +1♀ +[ELKU]; +Kumamoto +pref., +Yatsushiro dist. +, +Izumi +vill., +Shiratori +rindo + +, +9.VIII.1992 +. +1♂ +[ELKU]. + + + +Distribution. +Japan (Hokkaido; Honshu: Tokyo, Nagano, Gifu, and Tottori; Kyushu: Fukuoka and Kumamoto) + + +Etymology. +The species name refers to the yellow coxae. + + +Remarks. + +Among Japanese species, + +G. fulvicoxa + +sp. nov. is very similar to + +G. japonicum + +(Ashmead, 1904) in the sculpture of the head but differs from it in the shape of the horizontal portion of the occipital carina ( + +G. fulvicoxa + +(Fig. +4A +): straight, short; + +G. japonicum + +(Fig. +4B +): curved, relatively long), sculpture of mesopleuron (carinae of + +G. fulvicoxa + +(Fig. +2A +) stronger than + +G. japonicum + +(Fig. +2B +)) and the color of the coxae ( + +G. fulvicoxa + +(Fig. +2A +): yellow; + +G. japonicum + +(Fig. +2B +): brown). The sculpture of the frons in + +G. fulvicoxa + +(Fig. +4A +) is finer than that of + +G. japonicum + +(Fig. +4B +). Russian Far Eastern species, + +G. amissum + +Kozlov & Kononova, 1990, is also similar to + +G. fulvicoxa + +in the shape of the horizontal portion of the occipital carina. However, in + +G. amissum + +, the sculpture of frons is regularly arranged like + +G. yamagishii + +, the sculpture of mesopleuron is transversely costate with granulate sculptute between lower costae, mesopleural carina is weak, and the color of coxa is dark brown to black. +Talamas and Pham (2017) +provided images of type specimens of Vietnamese +Scelionidae +deposited in Institute of Ecology and Biological Resources, Hanoi, Vietnam, and we also examined these type specimens. According to these images and our examination, + +G. alames + +Kozlov & +Le +, 1996, + +G. avanus + +Kozlov & +Le +, 1996, and + +G. cromion + +Kozlov & +Le +, 1997 have a horizontal portion of the occipital carina similar to + +G. fulvicoxa + +. The color of coxa of these species are dark brown to black, however, that of + +G. fulvicoxa + +is yellow. + + + + \ No newline at end of file diff --git a/data/38/0A/87/380A87DC7A12FF8EDAA2FE5AB226FEEE.xml b/data/38/0A/87/380A87DC7A12FF8EDAA2FE5AB226FEEE.xml new file mode 100644 index 00000000000..dedfd924088 --- /dev/null +++ b/data/38/0A/87/380A87DC7A12FF8EDAA2FE5AB226FEEE.xml @@ -0,0 +1,520 @@ + + + +The family Opilioacaridae (Acari: Parasitiformes) in Argentina, with description of two new species + + + +Author + +Vázquez, Maria Magdalena +Universidad de Quintana Roo, Division de Ciencias e Ingenierias, Chetumal, Quintana Roo, Mexico. + + + +Author + +Bernardi, Leopoldo Ferreira de Oliveira +Bolsista do Programa Nacional de Pós-Doutorado (PNPD / CAPES), Departamento de Entomologia, Universidade Federal de Lavras (UFLA), Lavras, Minas Gerais, Brasil. + + + +Author + +Klompen, Hans +Acarology Laboratory, Ohio State University, 1315 Kinnear Road, Columbus, Ohio 43212 - 1192, U. S. A. + +text + + +Acarologia + + +2020 + +2020-06-16 + + +60 + + +3 + + +505 +519 + + + + +http://dx.doi.org/10.5281/zenodo.4361407 + +journal article +8351 +10.24349/acarologia/20204380 +f4d7fb98-abf1-418d-9ba7-ba5b66aecfc6 +2107-7207 +4503408 +522A7ACE-B100-4B92-8A80-72E17A6F59B7 + + + + + + + +Neocarus misiones + +n. sp. + + + + +Zoobank: +144FCF66-D9A1-4C22-AE7E-F45E462FD7B1 + + + + +Figures 1–4 +, +5 +A–B, 6–7, 8A + + + + +Diagnosis +— Palp genu with ~8 +p +- +type +setae, palp tarsus with 6 foliate setae with 4 rounded lobes each, and 15 +ch +- +type +sensilla. Sexual dimorphism in setation of prodorsal shield absent. Sternal setae +st2 +and +st3 +with attenuate tips. Pregenital region in male with 8–9 setae, mostly thick, ribbed and blunt, but a few lightly ribbed and tapering. Pregenital region in female without setae, genital region with 12–13 thick, lightly ribbed and barbed, tapering setae. Genital region in male with 7–9 barbed, lightly ribbed, tapering setae. Ovipositor without terminal sensilla but with three very distinct rounded terminal lobes and a bilobed membranous cover. + + + + +Description +— Description based on +4 females +and +4 males +. Immatures not available. + + +Gnathosoma + + +Chelicera +( +Figure 1A +). Basal segment in adults with 1 seta ( +cht +), fixed digit with 3, one of those ( + +ch1 + + +) large, thick. Seta +cht +on basal segment of male chelicera shorter than seta + +ch1 + + +on fixed digit. Setae + +ch2 + + +, + +ch2 + + +and +cht +in females and males simple, with an attenuated tip, lightly serrate. Number of the ventral denticles on movable digit in both female and male one ( +Figure 1A +, arrow). Axial scale-like processes on movable digit in both female and male absent. + + + +Figure 3 + +Neocarus misiones + + +n. sp. + +, prodorsal region: A – female (MACN-AR 4031/6) (grey arrow indicates lyrifissure); B – male (MACN-AR 4031/7). Scale bar 100 µm. Inset: detail anterior prodorsal setae. + + + +Subcapitulum +( +Figure 1B +). All four pairs of paralabial setae present: +pl1 +relatively large, conical, With + +s organ ( +pl2 +) membranous and discoid with a biramous core; rutellum +pl +( +3 +) with one row of 5 teeth, inserted dorso-lateral; +pl4 +small, inserted dorsal. With 4 circumbuccal ( +cb +) and 8–11 median and subcapitular +vm +(, +lvm +, +ldm +, +vp +, +lvp +) setae. Seta +vm1 +on the male subcapitulum present. Setae +vm1 +plus one more lateral setal pair with blunt tips in both sexes, all other subcapitular setae with attenuate tips. Females generally with more subcapitular setae (10–11) than males (8–9). Lateral lips in all instars with distinct canals ( +ogl1 +and +ogl2 +). + + +Palp +( +Figure 2 +). Trochanter with 4 large, ribbed, tapering setae (= +r +- +type +); femur with 9–13 papilliform (= +p +- +type +) and 15 +r +- +type +setae; genu with 8 +p +- +type +and 29 +r +- +type +setae; tibia with 30 long, lightly serrate and pointed setae, 27 +r +- +type +setae, and 2 long, thin, smooth sensilla. Tibia ventrally with one small indistinct gland; similar glands not observed for other palpal segments. Tibia and tarsus partially fused. Tarsus with 6 foliate +d +(- +type +), 8 +v +, 15 +ch +, and 9 +sm +sensilla, plus 3 solenidia (= +s +- +type +sensilla). Foliate sensilla each with 4 lobes with rounded, not filiform, tips. Modified +sm3 +- +type +sensilla on male palp tarsus absent. Lyrifissures iα and iπ (not drawn) present. Pretarsus in shape of a pair of well-developed, smooth, sessile claws. + + +Idiosoma + +Color. Dark blue and violet stripes on both body and legs. Body often with brownish background reflecting ingested food. + +Dorsum +. Prodorsal shield in adults with 142(M)–164(F) setae (N=1 for both) and two pairs of lateral eyes. One pair of prodorsal lyrifissures present ( +Fig 3A +, grey arrow). Setae somewhat rounded and “puffed-up” ( +Figure 3 +, detail). Sexual dimorphism in setal shape or setal arrangement minimal (setae in female appear slightly larger). Dorsal idiosoma between the shield and the preanal segment without setae, but with numerous lyrifissures arranged in transverse rows. Setation of preanal segment limited to 1 dorsal, and 2 ventro-lateral setae. Anal valves with 10–16 setae each, with females showing higher numbers. + + + +Figure 4 + +Neocarus misiones + + +n. sp. + +, sternitogenital area: A – female (MACN-AR 4031/5); B – male (MACN-AR 4031/8). Scale bar 100 µm. + + + + +Figure 5 + +Neocarus + +spp., details pregenital and genital setae. + +Neocarus misiones + + +n. sp +. + +A – genital setae female (MACN-AR 4031/6), B – genital and C – pregenital setae male (MACN-AR 28898/2); + +N. entrerios + + +n. sp. + +D – genital setae female (MACN-AR 28895/6), E – genital and F – pregenital setae male (MACN-AR/3). Scale bar 25 µm. + + + +Sternitogenital region +( +Figure 4 +). Sternal verrucae in adults each with 3–4 large, serrate and pointed, and 1 composite +St +( +1 +) seta. Setae +St1 +subequal in size to +St5 +. Setae +St2 +and +St3 +in females and males barbed, tapering to a fine tip. Remaining sternal region with 4–6 pairs of stout, ribbed, setae with rounded tips. Pregenital capsules each with 1 long, tapering seta ( +St5 +) and 4–6 stout, ribbed, blunt-tipped setae. Pregenital and genital areas in female with, respectively, 0 and 12–13 sturdy, lightly ribbed and barbed, tapering setae ( +Figure 5A +). Male with 8–9 setae in pregenital region, mostly thick, ribbed and blunt, but a few lightly ribbed and tapering. Genital region 7–9 barbed, lightly ribbed, tapering setae ( +Figure 5 +B–C). Ovipositor ( +Figure 6 +) without terminal setiform sensilla, but with three very distinct roundish terminal lobes. Without well sclerotized internal structures. Terminal area in one female (the only one where this area was fully visible) covered by a bilobed membrane/tectum ( +Figure 6A +, arrow). Male genital valves rectangular to curved, not triangular. Male glands well developed, both pairs of similar size ( +Figure 7 +). + + +Legs + + +Length of legs I–IV in females, respectively, 3937–4200, 2185–2302, 2106–2367, and 3240–3390 (N=3), for males slightly shorter, respectively 3114–4162, 2025–2315, 2184, and 3065 (N=1–3). Ratio of legs I to idiosoma in female approximately 1.8–1.9, legs IV to idiosoma about 1.5–1.7. Eupathidium ζ1 on tarsus I inserted in dorsal sensory field; simple, without enlarged tip ( +Figure 8A +). Smooth setae on tibia, genu and femur I absent in the male. Solenidion ω +a +on legs II positioned on acrotarsus; ω +a +on tarsi III–IV absent. Solenidion ω +d +on basitarsi II–IV inserted in apical portion, partially in a cup inside the segment. Tip of setae +ld +of ambulacra II–IV in male smooth and attenuate. Ventral portion of acrotarsi II–IV with 3 pairs of setae; lateral portion with 2 pairs distinctly lateral, plus 1 pair of ventro-lateral and one pair of dorso-lateral setae. Setae +lv +of acrotarsi II–IV with one, rarely two, small barbs. Papilliform setae on dorsal portion of the basitarsi II–III present; thin, smooth setae present in male, absent in female. Coronidia present on basitarsi II–IV in all adults, absent on tibiae and genua II–IV. The condition of the specimens (poor clearing) prevented making accurate counts of the smooth setae and coronidia. + + + +Figure 6 + +Neocarus misiones + + +n. sp. + +, female (MACN-AR 41730, holotype), ovipositor: A – composite drawing of several specimens (arrow indicates bilobed tectum), B – stacked image (MACN-AR 4031/1). Scale bar 100 µm. + + + +Collection information +— Type depository. +Holotype +female, MACN-AR 41730 (5 slides), MACN. +Paratypes +in OSAL (MACN-AR 4031/7) and MACN (all other). + + + +Locality +data. +Holotype +female, +MACN-AR 41730 +: +Argentina +, +Misiones +, +Iguazu +, +Puerto Libertad +, + +173m + +, +25.9189°S +54.5818°W +, + +Oct 1954 + +, coll. +Schiapelli +and +De Carlo +, + + +no data on habitat. +Same +collection data: one female, +MACN-AR 28898 +/3 (4 slides), + + +one male +MACN-AR 28898 +/2 (3 slides). +Same +locality, + +Oct 1953 + +, coll. +De Carlo +, +Schiapelli +, +Viana +and +Galiano +, ex area with palm trees: two females, MACN-AR 4031/5 (2 slides), MACN-AR 4031/6 (1 slide), two males, MACN-AR 4031/7, MACN-AR 4031/8 (1 slide each). + + + + + +Etymology +— The specific name is derived from the primary collection locality, +Misiones province +, +Argentina +. + + +Comparative notes +— This comparison is limited to described + +Neocarus + +species from South America, with exception of + +N. ojasti +Lehtinen, 1980 + +. The description of + +N. ojastii + +does not provide sufficient detail for an adequate comparison. Comparisons with + +N. platensis + +are based on the original description by +Silvestri (1905) +, the re-description by Van der +Hammen (1969) +based on Brazilian material, and comments and notes by Marcel Santos de Araújo based on examination of the +type +series. + + + +Neocarus misiones + +differs from + +N. coronatus + +Araújo +et al. +, 2018 + + +by the absence of distinct sexual differentiation in the setation of the prodorsal shield, and the presence of 6, rather than 4, +d +setae on the palp tarsus; from + +N. potiguar + +Bernardi +et al. +, 2012 + + +, + +N. proteus + +Bernardi +et al. +, 2013 + + +, and + +N. platensis + +by the absence, vs. presence, of pregenital setae in the female ( +Hammen, 1969 +; Araújo, pers. comm.). It differs from + +N. caipora +Bernardi +et al. +, 2014 + +and + +N. spelaion +Bernardi and Borges-Filho, 2018 + +by the different shape of the genital setae in the female (sturdy and ribbed vs. thin and smooth), and the presence of 4, rather than 3 lobes on the +d +setae on the palp tarsus ( + +N. caipora + +only). + + + + \ No newline at end of file diff --git a/data/38/0A/87/380A87DC7A15FF82DAA2FDDEB4CEFEAB.xml b/data/38/0A/87/380A87DC7A15FF82DAA2FDDEB4CEFEAB.xml new file mode 100644 index 00000000000..5987f711c55 --- /dev/null +++ b/data/38/0A/87/380A87DC7A15FF82DAA2FDDEB4CEFEAB.xml @@ -0,0 +1,144 @@ + + + +The family Opilioacaridae (Acari: Parasitiformes) in Argentina, with description of two new species + + + +Author + +Vázquez, Maria Magdalena +Universidad de Quintana Roo, Division de Ciencias e Ingenierias, Chetumal, Quintana Roo, Mexico. + + + +Author + +Bernardi, Leopoldo Ferreira de Oliveira +Bolsista do Programa Nacional de Pós-Doutorado (PNPD / CAPES), Departamento de Entomologia, Universidade Federal de Lavras (UFLA), Lavras, Minas Gerais, Brasil. + + + +Author + +Klompen, Hans +Acarology Laboratory, Ohio State University, 1315 Kinnear Road, Columbus, Ohio 43212 - 1192, U. S. A. + +text + + +Acarologia + + +2020 + +2020-06-16 + + +60 + + +3 + + +505 +519 + + + + +http://dx.doi.org/10.5281/zenodo.4361407 + +journal article +8351 +10.24349/acarologia/20204380 +f4d7fb98-abf1-418d-9ba7-ba5b66aecfc6 +2107-7207 +4503408 +522A7ACE-B100-4B92-8A80-72E17A6F59B7 + + + + + + +Genus + +Neocarus +Chamberlin and Mulaik, 1942 + + + + + + + +All specimens examined in this study are assigned to the genus + +Neocarus +Chamberlin and Mulaik, 1942 + +. Generic assignment is based on the following characteristics. In the adults 3 setae on the penultimate body segment (0 or> +3 in +all Old World taxa and + +Amazonacarus +Vázquez +et al. +, 2014 + +; shared with + +Caribeacarus +Vázquez and Klompen, 2009 + +and + +Brasilacarus + +Vázquez +et al. +, 2015 + + +), 4–6 foliate setae on the palp tarsus (> +7 in + +Caribeacarus + +and + +Brasilacarus + +), eupathidium zeta–1 (ζ1, the sensillum with a “crown-like” tip) in the main sensillar group of tarsus I (usually distal in + +Caribeacarus + +), and shiny fleshy setae with a whip-like tip absent from the palps (present in + +Brasilacarus + +). + + + +Figure 2 + +Neocarus misiones + + +n. sp. + +, female (MACN-AR 28898/3), palp, axial (left) and antiaxial (right) view: A – femur; B – genu; C, tibia; D, tarsus. Scale bars A–C: 100 µm, D: 50 µm. + + + +Within + +Neocarus + +the Argentinean specimens share a few characteristics suggesting that they may be related: palp tarsus in adults carries 6 large, foliate sensilla with 4 prominent lobes (usually 3 lobes) and both pairs of genital glands in the males are distinct, large, and similar in size (generally indistinct in cleared specimens, or anterior pair much smaller than posterior). + + + + \ No newline at end of file diff --git a/data/38/0A/87/380A87DC7A1EFF8DDAA2FE56B1C4FB7F.xml b/data/38/0A/87/380A87DC7A1EFF8DDAA2FE56B1C4FB7F.xml new file mode 100644 index 00000000000..3b423b480ab --- /dev/null +++ b/data/38/0A/87/380A87DC7A1EFF8DDAA2FE56B1C4FB7F.xml @@ -0,0 +1,337 @@ + + + +The family Opilioacaridae (Acari: Parasitiformes) in Argentina, with description of two new species + + + +Author + +Vázquez, Maria Magdalena +Universidad de Quintana Roo, Division de Ciencias e Ingenierias, Chetumal, Quintana Roo, Mexico. + + + +Author + +Bernardi, Leopoldo Ferreira de Oliveira +Bolsista do Programa Nacional de Pós-Doutorado (PNPD / CAPES), Departamento de Entomologia, Universidade Federal de Lavras (UFLA), Lavras, Minas Gerais, Brasil. + + + +Author + +Klompen, Hans +Acarology Laboratory, Ohio State University, 1315 Kinnear Road, Columbus, Ohio 43212 - 1192, U. S. A. + +text + + +Acarologia + + +2020 + +2020-06-16 + + +60 + + +3 + + +505 +519 + + + + +http://dx.doi.org/10.5281/zenodo.4361407 + +journal article +8351 +10.24349/acarologia/20204380 +f4d7fb98-abf1-418d-9ba7-ba5b66aecfc6 +2107-7207 +4503408 +522A7ACE-B100-4B92-8A80-72E17A6F59B7 + + + + + + + +Neocarus entrerios + +n. sp. + + + + +Zoobank: +19D08729-13CF-4DC3-8EDF-9BFED58D6B9E + + + + +Figures 5 +D–F, 8B, 9–13 + + + + +Diagnosis +— Palp genu without +p +- +type +setae, tarsus with 6 pairs of foliate setae with four rounded lobes each and 20 +ch +- +type +sensilla. Sexual dimorphism in setation of prodorsal shield distinct. Sternal setae +St2 +and +St3 +with attenuate tips. Pregenital area in males area with 6–10 stout, ribbed setae with relatively blunt tips, in genital area with 8–10 thinner, ribbed and tapering, setae. Females lacking pregenital setae, in genital area with 6–12 ribbed and tapering setae. Ovipositor lacking terminal sensilla, but with a very distinct pair of internal papillate hooks. + + + + +Figure 7 + +Neocarus misiones + + +n. sp. + +, male (MACN-AR 28895/2), glands. Scale bar 200 µm. + + + + +Figure 8 + +Neocarus + +spp., tip tarsus I: A – + +N. misiones + + +n. sp. + +, female (MACN-AR 4031/5); B – + +N. entrerios + + +n. sp. + +, female (MACN-AR 28895/5). Scale bar 50 µm. + + + + +Description +— Based on +4 females +and +3 males +. Immatures unknown. + + +Gnathosoma + + +Chelicera +( +Figure 9A +). Basal segment in adults with 1 seta, fixed digit with 3, one of which ( +ch1” +) distinctly larger. Seta +cht +on basal segment of male chelicera shorter than seta +ch1’’ +on fixed digit. Setae +ch2’ +, +ch2’’ +and +cht +in males simple, with an attenuated tip. One large, somewhat blunt, ventral denticle on movable digit in all adults. Axial scale-like processes on movable digit in both adults absent. + + +Subcapitulum +( +Figure 9B +). All four pairs of paralabial setae present: +pl1 +relatively large, conical, With + +s organ ( +pl2 +) membranous and discoid with a biramous core; rutellum +pl +( +3 +) with one row of 5 teeth, inserted dorso-lateral; +pl4 +small, inserted dorsal. With 4 circumbuccal ( +cb +) and 6–7 median and subcapitular +vm +(, +lvm +, +ldm +, +vp +, +lvp +) setae. Seta +vm1 +on the male subcapitulum present. Lateral lips with distinct canals ( +ogl1 +and +ogl2 +). + + +Palp +( +Figure 10 +). Trochanter with 3–4 ribbed, tapering setae (= +r +- +type +); femur with 4–9 ( +6–9 in +F; +3–6 in +M) papilliform (= +p +- +type +) and 13 +r +- +type +setae; genu with 0 +p +- +type +and 43 +r +- +type +setae; tibia with 21 long, lightly serrate and pointed setae, 38 +r +- +type +setae, and 2 long, thin, and smooth sensilla. Tibia and genu ventrally with a small indistinct gland. Tibia and tarsus partially fused. Tarsus with 6 foliate ( +d +- +type +), 10 +v +, 20 +ch +, and 10–12 +sm +sensilla, plus + + + +Figure 9 + +Neocarus entrerios + + +n. sp. + +A – partial chelicera, male (MACN-AR 28895/3); B – subcapitulum, female (MACN-AR 41735, holotype). + +Scale bar 100 µm. + + +3 solenidia (= +s +- +type +sensilla). Foliate setae each with 4 lobes and rounded, not filiform, tips. Modified +sm3 +- +type +sensilla on male palp tarsus absent. Lyrifissures iα and iπ distinct. Pretarsus in shape of a pair of well-developed sessile claws. + + +Idiosoma + +Color: Violet-blue with the usual banding pattern. Color observed for alcohol preserved specimens only. + +Dorsum +. Prodorsal shield with two pairs of lateral eyes. One pair of prodorsal lyrifissures present. Setation in females and males consisting of, respectively, 186–204 and 218–242 setae. Sexual dimorphism in anterior portion of prodorsal shield (between anterior margin and lyrifissures) distinct, with a dense grouping of 56–62 setae in males ( +Figure 11A +) vs. +22– 24 in +females ( +Figure 11B +). Setal density in anterior area of females similar to that on the remaining shield. All setae somewhat rounded in appearance and “puffed-up” ( +Figure 11 +, detail). Dorsal idiosoma between the prodorsal shield and the preanal segment without setae, but with numerous lyrifissures arranged in transverse rows. Setation preanal segment limited to 1 dorsal, and 2 ventro-lateral setae. Anal valves with 12–16 stout, ribbed setae ( +14–16 in +females; +12–16 in +males). + + +Sternitogenital region +( +Figure 12 +). Sternal verrucae in adults each with 2–3 large pointed, and 1 composite ( +St1 +) setae. Setae +St1 +subequal in size to +St5 +. Setae +St2 +and + +St +3 + +in females and males barbed, tapering to a fine tip. Remaining sternal region with 4–6 pairs of stout, ribbed setae with blunt tips. Pregenital capsules each with 1 long, tapering seta ( +St5 +) and 6–8 (female) or 5–6 (male) stout, ribbed setae. Pregenital and genital areas in female with, respectively, 0 and 6–12 smooth, tapering setae with rounded tip ( +Figure 5D +), male with, respectively, 6–10 stout, ribbed, and relatively blunt-tipped setae and 8–10 ribbed and tapering setae ( +Figure 5 +E–F). Ovipositor without terminal setiform sensilla, but ventrally with a pair of papillate, retrorse spines connected to a papillate ridge ( +Figure 13A +, arrow). More dorsally two sets of sclerotized ridges, with the middle one connecting to form a W-shaped structure ( +Figure 13B +, arrow). Male genital valves rectangular or curved, not triangular. + + + +Figure 10 + +Neocarus entrerios + + +n. sp. + +, palp tarsus, female (MACN-AR 41735, holotype): A – axial (left); B – antiaxial (right) view. Scale bar + + + +100 µm +. + + + + \ No newline at end of file diff --git a/data/38/0A/C0/380AC0E9F35837B7866A5AACE77D318E.xml b/data/38/0A/C0/380AC0E9F35837B7866A5AACE77D318E.xml new file mode 100644 index 00000000000..87f43f61dd4 --- /dev/null +++ b/data/38/0A/C0/380AC0E9F35837B7866A5AACE77D318E.xml @@ -0,0 +1,156 @@ + + + +Taxonomy of the thelyphonid genus Typopeltis Pocock, 1894, including homology proposals for the male gonopod structures (Arachnida, Thelyphonida, Typopeltinae) + + + +Author + +Seraphim, Gabriel + + + +Author + +Giupponi, Alessandro Ponce de Leao + + + +Author + +Miranda, Gustavo Silva de + +text + + +ZooKeys + + +2019 + +848 + + +21 +39 + + + + +http://dx.doi.org/10.3897/zookeys.848.32263 + +journal article +http://dx.doi.org/10.3897/zookeys.848.32263 +1313-2970-848-21 +BC8282C2C971453FB5212A1BA06D77DA +BC8282C2C971453FB5212A1BA06D77DA + + + + +Typopeltis laurentianus +sp. n. + + + +Type material. + +Holotype male: VIETNAM: +Ha +Tĩnh +, 18.355240, 105.886949, 1998 (MNRJ 08243). Paratypes: VIETNAM: +Ha +Tĩnh +, 18.355240, 105.886949, 1998 (2 males, MNRJ 08243); +Ha +Tĩnh +, 18.355240, 105.886949, 1997 (1 male, 1 female, MNRJ 08242); Quang Binh: Phong Nha-Kẻ +Bang +National Park, 17.590802, 106.283344, 2001 (1 male, MNHN AR-UR-2 [ex MNRJ 08244]; 1 female, CAS, CASENT 9081667 [ex MNRJ 08245]); +Vĩnh +Phuc +, 17.590802, 106.283344, x.1980, leg. R. Boistel (2 females, MNRJ 08246). + + + +Etymology. + +Species name +laurentianus +(laurentiana, laurentianum) is a Latin adjective after our friend, the distinguished Franco-Brazilian arachnologist Wilson +Lourenco +. The Latin form of Portuguese +Lourenco +is Laurentius (genitive +Laurentiī +), a noun of the second declension, cognate of English Lawrence or French Laurent. The ICZN allows authors of new species to choose the Latin version of contemporary names derived from Latin, which may be more euphonic than the modern counterparts. + + + + +Diagnosis +. + + +Males (about 35 mm in total length without flagellum) larger than females (see measurements); males with patellar apophysis very long, with narrow base and apex, broader in the middle, with a small antero-posterior curve. Patellar apophysis without spines in the trunk or the terminal portion, with a smooth integument texture that differs from all the other species of +Typopeltis +. The male gonopod is simple, delimited by a sclerotized curved cuticle (posterior apex of Fi), with inverted trapezoid shape with rounded edges. The female gonopod has a bulbous RS with a wide base and a well marked CCh. + + + +Description. +(Holotype male) Colouration (in alcohol). Reddish-brown. Carapace darker on anterior region than posterior region. Abdomen slightly yellowish. Pedipalps dark red, lighter in females lighter. Median eyes dark, almost black, lateral eyes yellow. +Carapace (Figs 1A, 2A). With thick granules of irregular shapes homogeneously covering whole surface, granules interspaced. Lateral keel with one seta on each anterior end, next to median eyes; posterior end of keels above lateral triad of eyes, keel extends from posterior to anterior region of carapace; keels divided by median ocular ridge. Carapace has depression extending from posterior region of median ocular tubercle to region above subtriangular fovea. Median eye tubercle elevated, with well-marked ridge between eyes. Chelicerae with several setae in ventral region and on cheliceral claw. Cheliceral claw curved inwards, with thick base and narrow apex, and with short keel, smaller than half length of tooth (Fig. 3A). + + +Figure 1. +Typopeltis laurentianus +sp. n., holotype (male). A Carapace B sternum C pedipalps (dorsal) D pedipalps (ventral) E opisthosoma (dorsal) F opisthosoma (ventral) G ommatoid H gonopod. + + + + +Figure 2. +Typopeltis laurentianus +sp. n., paratype (female). A Carapace B sternum C pedipalps (dorsal) D pedipalps (ventral) E opisthosoma (dorsal) F opisthosoma (ventral) G ommatoid H gonopod. CCh = circulus chitinosus; ACh = arcus chitinosus. + + + + +Figure 3. SEM images of +Typopeltis laurentianus +sp. n., paratype (male). A Chelicerae (right) B gonopod. Details in dashed rectangles are shown in images C (lower rectangle) and D (upper rectangle). C Fulcrum (Fu) detail D Mensa (Me) detail. + + +Sternum (Figs 1B, 2B). Typical of order, tri-segmented; inconspicuous mesosternum. + +Opisthosoma (Figs 1E, G; 2E, G). Pleura divided by crest of granules from tergites +I-VIII +; tergites without suture. Sides with fine granules (Figs 1E, 2E). Subcircular ommatoids present (Figs 1G, 2G). Flagellum with 38 articles (female paratype) and 36 in holotype (broken). + + +Pedipalps (Figs 1C, D; 2C, D). Coxa without accessory tooth, with few setae. Trochanter punctated with granules covering dorsal surface. Four spines in dorso-mesal region (I <II <III <IV), spines I-III as broad as or broader than long, conical, with broad base and acute apex; spine IV geminate with spine III, with long setae, conical; apex rhomboid and bigger than double size of spine III. Two small spines close to articular condyle (trochanter-femur), spines smaller than mesal spine I (Fig. 1C). Ventral region with thick ridge all along joint with femur, ending mesally with two small conical spines, broader than long (Fig. 1D). Femur unarmed and covered with shallow pores concentrated on outer margin (Fig. 1D). Ventro-mesal region with reduced rhombus spine (almost a granule), conical, broader than long, surrounded by long setae (Fig. 1C). In females, ventro-mesal spine well developed, twice longer than wide, with very sharp, curved tip and broad base. Two small conical spines dorsally (I <II); in males these spines reduced to two small granules, clearly homologous to spines present in females. Patella covered by pores, especially on ectal face, with few setae; several setae mesally. Patellar apophysis almost as long as patella, with large non-terminal (median) expansion on external margin of apophysis (like large hump); unprecedented smooth texture and slight curvature in ventral direction on terminal portion. Apophysis with spatulated shape with slight concavity ventrally. Ventral face without spines. Females with two coni +cal +spines of subequal size in dorso-mesal view (Fig. 2C); spines as broad as long, with broad base and sharp tip, most anterior at base of apophysis. Ventral apophysis with reduced ventro-mesal spine in distal position (Fig. 2D). Patellar apophysis well developed, but slightly smaller than length of patella, conical, tapering towards apex; with single spine on mesal surface, positioned just before apex; row of spines with three or four small subequal basal spines on ectal face, followed by median series of four spines increasing in size; second series of spines larger than double first row of spines; distal series composed of three spines, with middle ones larger than two others. Two rows of setae at edges of ventral region, absent in males. Tibia covered by pores, large concentration of setae (in mesal view), more than in femur and patella. Tibial apophysis conically-shaped, broad base, acute apex, with series of dorsal spines. In ventro-mesal view with two small spines, most apical rhombic and double the size of previous one; penultimate spine with conical shape, with wide base. Tarsus covered by long setae, with greater predominance on mesal surface. With longitudinal series of ventral rhomboid spines and another dorsal series. + + +Leg I. Eight tarsomers (variation: seven to nine), first very short (like small ring), second, third and last larger than others (I <II> +III-VII +<VIII); size and number of tarsomers can vary if leg is regenerated. Apical portion of tibia with two dorsolateral tricobothria, absent in femur and patella. Femur covered with thick granules, patella and tibia with smooth appearance. All articles covered with setae dorsally and ventrally. + + +Legs +II-IV +. Trochanter and femur with granules. Coxa, tibia and tarsus smooth, last two with concentration of setae. With dorso-apical tricobothrium on tibia; ventro-apical region with thin, acuminate spur. Basitarsus with two spurs, one mesal and other ectal; ventral region with two longitudinal rows with four or five spiniform setae. Distitarsus divided into three tarsomers (I> II <III), length of tarsomere I equal or greater than II + III. Tarsomere I with two longitudinal rows with eight spiniform setae. Tarsomeres II and III similar to previous, but with three and four setae, respectively. + +Sternite (Figs 1F, 2F). Genital plate about 1.5 times wider than long, with irregularly distributed setae and accumulated pores on sides. Other ventrites mostly smooth. +Male Gonopod (Figs 1H; 3B, C, 3D). LoL1 broader than long, reniform, with thin longitudinal sclerotized wrinkles, slightly curved and sinuous in terminal portion (Fig. 1H); Fi with sclerotized borders and inverted trapezoid shape with rounded edges. LoD with strongly sclerotized acute projection positioned above all other gonopod structures. LoL2 globose, soft, partially covered by LoL1; LaM as two parallel plates originating in Me and supported by Fu (Fig. 3C). Me subtriangular and covered by denticles (Fig. 3D). Female Gonopod (Fig. 2H) with seminal receptacle (RS) of bulbous shape, with base slightly narrower than more dilated distal portion; longer than wide; concave chitinous arc with two sclerotized chitinous rings at base of RS. Two well-sclerotized structures on sides of chitinous arch, very long and thin, slightly curved inwards, with base wider than apex. + + +Measurements. +(holotype male before brackets, variation inside brackets). +Prosoma: 13.6 mm (length) [12.0-13.6 mm], 8.0 mm (width) [7.1-8.0 mm]; Opisthosoma: 19.4 mm (length) [17.5-19.4mm], 10.7 mm (width) [8.3-10.7mm]; Pedipalp: Trochanter: 4.2 mm [3.7-4.2 mm]; Femur: 4.0 mm [4.0-4.4mm]; Patella: 5.4 mm [4.8-5.4 mm]; Patellar apophysis: 4.4 mm [4.0-4.4 mm]; Tibia: 4.1 mm [3.0-4.1 mm]; Tibial apophysis: 1.7 mm [1.6-1.8 mm]; Tarsus: 3.1 mm [2.6-3.1 mm]. + + + \ No newline at end of file diff --git a/data/38/0B/41/380B418206B45B2FBB2F833BEFD47B61.xml b/data/38/0B/41/380B418206B45B2FBB2F833BEFD47B61.xml new file mode 100644 index 00000000000..eff97b3f2a5 --- /dev/null +++ b/data/38/0B/41/380B418206B45B2FBB2F833BEFD47B61.xml @@ -0,0 +1,252 @@ + + + +On eleven species of jumping spiders from Xishuangbanna, China (Araneae, Salticidae) + + + +Author + +Wang, Cheng +Guizhou Provincial Key Laboratory for Biodiversity Conservation and Utilization in the Fanjing Mountain Region, Tongren University, Tongren, Guizhou 554300, China + + + +Author + +Li, Shuqiang +https://orcid.org/0000-0002-3290-5416 +Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China +lisq@ioz.ac.cn + +text + + +ZooKeys + + +2022 + +2022-08-08 + + +1116 + + +85 +119 + + + + +http://dx.doi.org/10.3897/zookeys.1116.82858 + +journal article +http://dx.doi.org/10.3897/zookeys.1116.82858 +1313-2970-1116-85 +28FBF60795F24E60AE387439D84DE527 +A6538A8A74C35AD0AA817B1EBFDE153F + + + + +Rhene triapophyses Peng, 1995 + + + + +Figs 14 +, 15 + + + + +Rhene triapophyses +Peng, 1995: 35, figs 1-5 (male holotype, not examined); +Peng 2020 +: 395, fig. 288a-e. + + + +Material examined. + + +1♂ +3♀ +(IZCAS-Ar42943-42946), +China +: +Yunnan +, +Xishuangbanna +, +Mengla County +, +Menglun Town +, +Xishuangbanna Tropical Botanical Garden +, +Yulinjiegou +( +21°55.05'N +, +101°16.24'E +, ca + +570 m + +alt.), +19.xii.2018 +, +X. Mi +et al. leg + +.; + +1♂ +1♀ +(IZCAS-Ar42947-42948), 1 site in +Mafengzhai +( +21°53.45'N +, +101°17.40'E +, ca + +543 m + +alt.), +29.ix.2019 +, +Y. Tong +et al. leg + +. + + + +Diagnosis. + + +Rhene triapophyses + +Peng, 1995 closely resembles that of + +R. setipes + +Zabka +, 1985 from China, Vietnam and Japan in the general shape of the habitus and copulatory organs, but it differs in the following: 1) embolic division includes two terminal apophyses (Fig. +14B +) versus only one terminal apophysis in + +R. setipes + +( + +Zabka +1985 + +: fig. 563); 2) anteromedially, retrolateral tibial apophysis extending antero-retrolaterally (Fig. +14C +) versus extending antero-prolaterally in + +R. setipes + +( + +Zabka +1985 + +: fig. 564); 3) female almost indistinguishable from + +R. setipes + +except in the form of the copulatory ducts and atria (Fig. +15A-C +vs +Tanikawa 1993 +: figs 10, 11). + + + +Figure 14. + +Rhene triapophyses + +, male palp +A +prolateral +B +ventral +C +retrolateral. Scale bars: 0.1. + + + + +Description. + +Male +(Figs +14 +, +15D, E, G-I +). Total length 4.07. Carapace 1.93 long, 1.90 wide. Abdomen 2.30 long, 1.83 wide. Clypeus 0.08 high. Eye sizes and inter-distances: AME 0.42, ALE 0.22, PLE 0.20, AERW 1.43, PERW 1.87, EFL 1.24. Legs: I 4.66 (1.63, 1.85, 0.68, 0.50), II 3.19 (1.08, 1.13, 0.58, 0.40), III 2.98 (1.00, 0.98, 0.60, 0.40), IV 3.88 (1.33, 1.40, 0.75, 0.40). Carapace red-brown to dark brown, almost hexagonal, with large, irregular dark brown patch at center of eye field, covered with dense setae. Fovea indistinct. Chelicerae red-brown, with two promarginal teeth and one retromarginal tooth, the paturon covered by papillae, with distinct incision on anterior surface. Endites typical, bearing dark setae entally. Labium darker than endites. Sternum almost oval, bearing pale, thin setae. Legs I strongest, with enlarged femora, two pairs of ventral spines on tibia and three ventral spines on metatarsi, other legs yellow to dark brown, with slightly enlarged femora. Abdomen suboval, dorsum red-brown, yellow posteriorly, with an irregular, longitudinal dark patch anteromedially followed by a broad, transverse, dark brown band, covered with short, pale white, thin setae and wholly covered by large scutum; venter brown, with a pair of longitudinal, dark stripes medially. + + + +Figure 15. + +Rhene triapophyses + +A, B +epigyne, ventral +C +vulva, dorsal +D +male habitus, dorsal +E +ditto, ventral +F +female habitus, dorsal +G +male carapace, frontal +H +male chelicera, posterior +I +male leg I, prolateral. Scale bars: 0.1 ( +A-C, H +); 0.5 ( +D-F, I +); 0.2 ( +G +). + + + +Palp (Fig. +14A-D +): tibia almost as long as wide, with tapered retrolateral apophysis distally curved inward to a pointed tip; cymbium about 1.5 times longer than wide; bulb slightly swollen posteromedially, with tapered sperm duct, sinuous retrolaterally; embolus originating from middle of anterior margin of bulb, bar-shaped, blunt apically, division with two spiny apophyses. + + +Female +(Fig. +15A-C, F +). Total length 4.32. Carapace 2.04 long, 1.96 wide. Abdomen 2.50 long, 1.86 wide. Clypeus 0.08 high. Eye sizes and inter-distances: AME 0.40, ALE 0.22, PLE 0.20, AERW 1.43, PERW 1.96, EFL 1.29. Legs: I 4.00 (1.45, 1.55, 0.55, 0.45), II 3.13 (1.08, 1.15, 0.50, 0.40), III 3.08 (1.03, 1.05, 0.60, 0.40), IV 4.09 (1.33, 1.53, 0.83, 0.40). Habitus similar to that of male except paler and without dorsal scutum on abdomen. + + +Epigyne (Fig. +15A-C +): wider than long, with broad posterior hood distant from epigastric furrow; atria paired, oval, separated from each other by slightly more than width of epigynal hood; copulatory ducts long, transversely extending before curving 90° then descending posteriorly, continuing into an S-shaped coil; spermathecae indistinct; fertilization ducts lamellar, extending anterolaterally. + + + +Distribution. +China (Yunnan). + + +Comments. +The male of the new material is almost identical with the holotype in palpal and cheliceral structure except detail difference in the length of the apophyses of embolic division. Moreover, material studied in this paper were collected from the same locality as holotype in Menglun County, Xishuangbanna, China. + + + \ No newline at end of file diff --git a/data/38/0B/B1/380BB1E3B7F5AECF37F45C4C824B1EDD.xml b/data/38/0B/B1/380BB1E3B7F5AECF37F45C4C824B1EDD.xml new file mode 100644 index 00000000000..d7aa2b463cf --- /dev/null +++ b/data/38/0B/B1/380BB1E3B7F5AECF37F45C4C824B1EDD.xml @@ -0,0 +1,110 @@ + + + +The ground beetles (Coleoptera: Carabidae) of the Strandzha Mountain and adjacent coastal territories (Bulgaria and Turkey) + + + +Author + +Kostova, Rumyana + + + +Author + +Gueorguiev, Borislav + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8135 +8135 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8135 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8135 +1314-2828--8135 + + + + +Bembidion (Phyla) tethys Netolitzky, 1926 + + + +Materials + + +Type status: +Other material +. Occurrence: recordedBy: +R. Kostova +; individualCount: +1 +; Location: countryCode: BG; locality: +Kosti Vill., "St. Ilia" Place +; verbatimElevation: +35 +; verbatimCoordinates: +N42°03'23.2" +, +E27°45'51.6" +; geodeticDatum: WGS84; Event: eventDate: +09.06-02.07.2009 +; habitat: meadow with single trees + + +Type status: +Other material +. Occurrence: recordedBy: +R. Kostova +; individualCount: +1 +; Location: countryCode: BG; locality: +Sinemorets Vill., PA"Silistar", "Butamyata" Place +; verbatimElevation: +10 +; verbatimCoordinates: +N42°03'11.2" +, +E27°59'19.7" +; geodeticDatum: WGS84; Event: eventDate: +15.04-08.05.2009 +; habitat: meadow, single shrubs + + +Type status: +Other material +. Occurrence: recordedBy: +R. Kostova +; individualCount: +1 +; Location: countryCode: BG; locality: +Sinemorets Vill., PA"Silistar", "Butamyata" Place +; verbatimElevation: +10 +; verbatimCoordinates: +N42°03'11.2" +, +E27°59'19.7" +; geodeticDatum: WGS84; Event: eventDate: +03.07-02.08.2009 +; habitat: meadow, single shrubs + + + + + \ No newline at end of file diff --git a/data/38/0B/DA/380BDA1FBCBF858908FC014A62654628.xml b/data/38/0B/DA/380BDA1FBCBF858908FC014A62654628.xml new file mode 100644 index 00000000000..d6f8929614d --- /dev/null +++ b/data/38/0B/DA/380BDA1FBCBF858908FC014A62654628.xml @@ -0,0 +1,165 @@ + + + +Isotomidae of Japan and the Asiatic part of Russia. I. Folsomia ' inoculata' group + + + +Author + +Potapov, Mikhail + + + +Author + +Hasegawa, Motohiro + + + +Author + +Kuznetsova, Natalia + + + +Author + +Babenko, Anatoly + + + +Author + +Kuprin, Alexander + +text + + +ZooKeys + + +2018 + +750 + + +1 +40 + + + + +http://dx.doi.org/10.3897/zookeys.750.22764 + +journal article +http://dx.doi.org/10.3897/zookeys.750.22764 +1313-2970-750-1 +B10B5506EF9F477480F4BC5A776FA266 +B10B5506EF9F477480F4BC5A776FA266 + + + + + +Folsomia +trisensilla Potapov + +sp. n. +Figs 50, 53, 58-64, 90 + + + +Type material. + +Holotype, female, Far East of Russia, Khabarovsky Krai, Vaninsky District, 10 km N Vysokogorny, valley of Mulinka River, closed +Picea +and +Abies +forest on NE slope, litter, ~ 750 m alt., 29.ix.2011, coll. M. Potapov. Ten paratypes from the same location and six paratypes from the nearly same location, in litter of coniferous forests at different altitudes (600 and 900 m alt.), 29.ix.2011, coll. M. Potapov. Deposited in MSPU. + + + +Other material. + +Far East of Russia, Khabarovsky Krai. Different sites of type locality, litter and rotten wood, 29.ix.2011, coll. M. Potapov; Kamchatka. Nearby Anavgai and Esso settlements, different larch forests, litter and rotten wood, ~ 500 m alt., 4.vii.2012, coll. M. Potapov; Primorsky Krai. Terneysky District, Sikhote-Alimski Reserve, Kabany station, forest litter, 08.viii.2017, coll. N. Kuznetsova, A. +Geras'kina +, A. Kuprin; East Siberia: Chitinskaya Region, near foothills of Daursky Range, valley of Ilya River, ~ three km station Ara-Ilya, +50.9253°N +, +113.1783°E +, 887 m alt., mixed forest with +Betula +and +Larix +, 11.vii.2014, coll. A. Gulgenova. + + + +Diagnosis. +Blind. Dorsal macrosetae (Md) present on both Th.II and Th.III. Sensillary formula incomplete (33/22224; 10/000). Medial s-setae on body tergites long, set in p-row. Ventral setae on Th.III present. Anterior side of manubrium with 3+3 paired setae, no unpaired axial setae present. Dens with 12-16 anterior setae, its posterior side with four setae in basal part. Mucro bidentate. + + +Description. + +Body size from 1.0 to 1.3 mm, rather tubular (Fig. 50). Without pigmentation. Cuticle +"smooth" +. PAO slender, slightly constricted, 1.5-1.7 as long as width of Ant.I and 1.7-2.0 as long as inner unguis length (Fig. 62). Labium complete, guard setae e7 present, three proximal and four basomedian setae. Ventral side of head with 4+4 postlabial setae. Ant.I with 15-16 common setae, two ventral s-setae (s) and three basal micro s-setae (bms): two dorsal (short and long) and one ventral. Ant.II with three bms and one latero-distal s, Ant.III with one bms and with five distal s (including one lateral), without additional s-setae. Several s-setae on Ant.IV tubular. Organite middle-sized, roundish. + + +Common +setae long. Sensillary formula as 33/22224 (s), three s-setae lost (as described for the ' +laconica +' subgroup (Figs 58, 59). Corner s-setae on Th.II absent (Fig. 60). Micro s-setae as 10/000 (ms). Tergal s-setae thin and long, lateral s-setae on abdomen shorter. Medial s-setae on Th. +II-Abd +.III situated in posterior position, on Abd. +I-III +between Md and Mdl. Abd.V with four s-setae arranged as three long and slender (accp1, accp2, accp3) and one latero-ventral, short ( +'3+1' +pattern) (Figs 53, 61), accp3 s-setae as long as accp2 (0.9-1.1). Macrosetae smooth and long, 2,2/3,3,3 in number, medial ones on Abd.V slightly shorter than dens (1.0-1.3) and 3.5-4.6 times longer than mucro. Metathorax with 3+3 ventral setae. + + +Empodial appendage as long as 0.5-0.6 of unguis. All tibiotarsi with additional setae: 24-26 on legs +I-II +and 30-35 on leg III. Upper and lower subcoxae of legs +I-III +with 0,1/3,7 +-8/6-7,7- +8 setae, respectively. Coxae of leg I with three (rarely two on one side) front setae. Tibiotarsal tenent setae pointed, some setae of distal whorl of tibiotarsi thickened. Ventral tube with 4+4 latero-distal and 7-8 posterior setae (four in distal transversal row and 3-4 in more proximal position), anteriorly without setae. Tenaculum with 4+4 teeth and a seta. Anterior furcal subcoxae with 8-10, posterior one with four setae. Anterior side of manubrium with 3+3 setae (rarely 2+3) (Fig. 63). Posterior side of manubrium with 5(4)+5(4) latero-basal, two apical setae (ap), 2+2 setae in distal transversal row (M1, ml1), two pairs of lateral setae, and 4 +-6+4- +6 in central part (Fig. 63). Dens with 12-16 anterior setae. Posterior side of dens crenulated and with five setae (4 basal and one shorter one at the base of mucro), two setae at the middle present or absent (Figs 63, 64, see also the Discussion part). Mucro bidentate. Ratio of manubrium: dens: mucro = 4.1-5.0: 3.9-5.2: 1. + + + +Figures 58-64. +F. trisensilla +sp. n. 58-59 Position of macrosetae, setae of p-row, and s-setae on anterior (58) and posterior (59) half of corpus 60Th.II 61 End of abdomen 62PAO and Ant.I 63 Furca, lateral view (type population) 64 Dens, lateral view (Kamchatka). + + + + +Remarks. +Two setae at the middle of posterior side of dens are always absent in the type populations (Fig. 63, Khabarovsky Krai). Specimens from Kamchatka possess these setae (always rudimentary and one sometimes asymmetrically lost) (Fig. 67). We accept a wide diagnosis of the new species considering both variants. +An odd population was found near Uril (Amurskaya Region) differing from the typical ones by having 4+4 (vs 3+3) anterior setae on manubrium (left out of diagnosis of the new species so far). + +For difference between +F. trisensilla +sp. n. and +F. laconica +sp. n. see Remarks to the latter. + + + +Distribution and ecology. +Known from forest litter in three localities in Eastern Asia (Fig. 90). + + +Derivatio nominis. + +The new species name reflects the presence of three (vs four, as common for the genus) s-setae on dorsal side of Abd.V that is characteristic of the ' +laconica +' subgroup. + + + + \ No newline at end of file diff --git a/data/38/0B/DC/380BDCEE0AC94DC37B710171C7A9D53E.xml b/data/38/0B/DC/380BDCEE0AC94DC37B710171C7A9D53E.xml new file mode 100644 index 00000000000..17db157bfbf --- /dev/null +++ b/data/38/0B/DC/380BDCEE0AC94DC37B710171C7A9D53E.xml @@ -0,0 +1,291 @@ + + + +Inventory of the Heteroptera (Insecta: Hemiptera) in Komaba Campus of the University of Tokyo, a highly urbanized area in Japan + + + +Author + +Ishikawa, Tadashi + + + +Author + +Saito, Masayuki U. + + + +Author + +Kishimoto-Yamada, Keiko + + + +Author + +Kato, Toshihide + + + +Author + +Kurashima, Osamu + + + +Author + +Ito, Motomi + +text + + +Biodiversity Data Journal + + +2015 + +3 + + +4981 +4981 + + + + +http://dx.doi.org/10.3897/BDJ.3.e4981 + +journal article +http://dx.doi.org/10.3897/BDJ.3.e4981 +1314-2828-3-4981 + + + + +Cysteochila consueta Drake, 1948 + + + +Materials + + +Type status: +Other material +. Occurrence: recordedBy: +T. Ishikawa +; individualCount: +2 +; sex: +1 male +, +1 female +; lifeStage: +adult +; otherCatalogNumbers: 2014-00943 | 2014-00944; Taxon: namePublishedIn: 1948; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hemiptera; family: Tingidae; genus: Cysteochila; specificEpithet: consueta; scientificNameAuthorship: Drake; Location: country: +Japan +; stateProvince: Tokyo; municipality: Meguro-ku; locality: +The University of Tokyo Campus, Komaba. +; minimumElevationInMeters: 31; maximumElevationInMeters: 39; decimalLatitude: +35.66006 +; decimalLongitude: +139.68521 +; geodeticDatum: WGS84; Identification: identifiedBy: T. Ishikawa; dateIdentified: 2013; Event: samplingProtocol: +net sweeping +; eventDate: +2013-05-12 +; Record Level: institutionCode: +KMUT +; collectionCode: +IC + + + + +Type status: +Other material +. Occurrence: recordedBy: +T. Ishikawa +; individualCount: +25 +; sex: +14 males +, +11 females +; lifeStage: +adult +; otherCatalogNumbers: 2014-00945 | 2014-00946 | 2014-00947 | 2014-00948 | 2014-00949 | 2014-00950 | 2014-00951 | 2014-00952 | 2014-00953 | 2014-00954 | 2014-00955 | 2014-00956 | 2014-00957 | 2014-00958 | 2014-00959 | 2014-00960 | 2014-00961 | 2014-00962 | 2014-00963 | 2014-00964 | 2014-00965 | 2014-00966 | 2014-00967 | 2014-00968 | 2014-00969; Taxon: namePublishedIn: 1948; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hemiptera; family: Tingidae; genus: Cysteochila; specificEpithet: consueta; scientificNameAuthorship: Drake; Location: country: +Japan +; stateProvince: Tokyo; municipality: Meguro-ku; locality: +The University of Tokyo Campus, Komaba. +; minimumElevationInMeters: 31; maximumElevationInMeters: 39; decimalLatitude: +35.66006 +; decimalLongitude: +139.68521 +; geodeticDatum: WGS84; Identification: identifiedBy: T. Ishikawa; dateIdentified: 2013; Event: samplingProtocol: +net sweeping +; eventDate: +2013-05-18 +; Record Level: institutionCode: +KMUT +; collectionCode: +IC + + + + +Type status: +Other material +. Occurrence: recordedBy: +T. Ishikawa +; individualCount: +2 +; sex: +2 females +; lifeStage: +adult +; otherCatalogNumbers: 2014-00970 | 2014-00971; Taxon: namePublishedIn: 1948; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hemiptera; family: Tingidae; genus: Cysteochila; specificEpithet: consueta; scientificNameAuthorship: Drake; Location: country: +Japan +; stateProvince: Tokyo; municipality: Meguro-ku; locality: +The University of Tokyo Campus, Komaba. +; minimumElevationInMeters: 31; maximumElevationInMeters: 39; decimalLatitude: +35.66006 +; decimalLongitude: +139.68521 +; geodeticDatum: WGS84; Identification: identifiedBy: T. Ishikawa; dateIdentified: 2013; Event: samplingProtocol: +net sweeping +; eventDate: +2013-08-15 +; Record Level: institutionCode: +KMUT +; collectionCode: +IC + + + + +Type status: +Other material +. Occurrence: recordedBy: +T. Ishikawa +; individualCount: +1 +; sex: +1 female +; lifeStage: +adult +; otherCatalogNumbers: 2014-00972; Taxon: namePublishedIn: 1948; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hemiptera; family: Tingidae; genus: Cysteochila; specificEpithet: consueta; scientificNameAuthorship: Drake; Location: country: +Japan +; stateProvince: Tokyo; municipality: Meguro-ku; locality: +The University of Tokyo Campus, Komaba. +; minimumElevationInMeters: 31; maximumElevationInMeters: 39; decimalLatitude: +35.66006 +; decimalLongitude: +139.68521 +; geodeticDatum: WGS84; Identification: identifiedBy: T. Ishikawa; dateIdentified: 2013; Event: samplingProtocol: +net sweeping +; eventDate: +2013-08-18 +; Record Level: institutionCode: +KMUT +; collectionCode: +IC + + + + +Type status: +Other material +. Occurrence: recordedBy: +T. Ishikawa +; individualCount: +2 +; sex: +2 females +; lifeStage: +adult +; otherCatalogNumbers: 2014-00973 | 2014-00974; Taxon: namePublishedIn: 1948; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hemiptera; family: Tingidae; genus: Cysteochila; specificEpithet: consueta; scientificNameAuthorship: Drake; Location: country: +Japan +; stateProvince: Tokyo; municipality: Meguro-ku; locality: +The University of Tokyo Campus, Komaba. +; minimumElevationInMeters: 31; maximumElevationInMeters: 39; decimalLatitude: +35.66006 +; decimalLongitude: +139.68521 +; geodeticDatum: WGS84; Identification: identifiedBy: T. Ishikawa; dateIdentified: 2013; Event: samplingProtocol: +net sweeping +; eventDate: +2013-09-06 +; Record Level: institutionCode: +KMUT +; collectionCode: +IC + + + + +Type status: +Other material +. Occurrence: recordedBy: +T. Ishikawa +; individualCount: +2 +; sex: +2 females +; lifeStage: +adult +; otherCatalogNumbers: 2014-00975 | 2014-00976; Taxon: namePublishedIn: 1948; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hemiptera; family: Tingidae; genus: Cysteochila; specificEpithet: consueta; scientificNameAuthorship: Drake; Location: country: +Japan +; stateProvince: Tokyo; municipality: Meguro-ku; locality: +The University of Tokyo Campus, Komaba. +; minimumElevationInMeters: 31; maximumElevationInMeters: 39; decimalLatitude: +35.66006 +; decimalLongitude: +139.68521 +; geodeticDatum: WGS84; Identification: identifiedBy: T. Ishikawa; dateIdentified: 2013; Event: samplingProtocol: +net sweeping +; eventDate: +2013-10-21 +; Record Level: institutionCode: +KMUT +; collectionCode: +IC + + + + +Type status: +Other material +. Occurrence: recordedBy: +T. Ishikawa +; individualCount: +2 +; sex: +1 male +, +1 female +; lifeStage: +adult +; otherCatalogNumbers: 2014-00977 | 2014-00978; Taxon: namePublishedIn: 1948; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hemiptera; family: Tingidae; genus: Cysteochila; specificEpithet: consueta; scientificNameAuthorship: Drake; Location: country: +Japan +; stateProvince: Tokyo; municipality: Meguro-ku; locality: +The University of Tokyo Campus, Komaba. +; minimumElevationInMeters: 31; maximumElevationInMeters: 39; decimalLatitude: +35.66006 +; decimalLongitude: +139.68521 +; geodeticDatum: WGS84; Identification: identifiedBy: T. Ishikawa; dateIdentified: 2013; Event: samplingProtocol: +net sweeping +; eventDate: +2013-10-30 +; Record Level: institutionCode: +KMUT +; collectionCode: +IC + + + + + \ No newline at end of file diff --git a/data/38/0C/5E/380C5E166B054B5D14ED506D84F78636.xml b/data/38/0C/5E/380C5E166B054B5D14ED506D84F78636.xml new file mode 100644 index 00000000000..fe7c47fe18b --- /dev/null +++ b/data/38/0C/5E/380C5E166B054B5D14ED506D84F78636.xml @@ -0,0 +1,104 @@ + + + +New Staphylinidae (Coleoptera) records with new collection data from New Brunswick, Canada: Scaphidiinae, Piestinae, Osorinae, and Oxytelinae + + + +Author + +Webster, Reginald P. + + + +Author + +Sweeney, Jon D. + + + +Author + +DeMerchant, Ian + +text + + +ZooKeys + + +2012 + +186 + + +239 +262 + + + + +http://dx.doi.org/10.3897/zookeys.186.2506 + +journal article +http://dx.doi.org/10.3897/zookeys.186.2506 +1313-2970-186-239 + + + + + +Baeocera inexspectata +Loebl +and Stephan, 1993** + +Map 3 + + + +Material examined. + +New Brunswick, Charlotte Co., S of Little Pocologan River, +45.1546°N +, +66.6254°W +, 7.V.2007, R. P. Webster, mature eastern white cedar swamp/forest, in moss and leaf litter (1 ♂, RWC). Sunbury Co., Acadia Research Forest, +46.0188°N +, +66.3765°W +, 18.VI.2007, R. P. Webster, mature red spruce and red maple forest, sifting leaf litter and moss (2 ♂, RWC). + + + +Map 3. Collection localities in New Brunswick, Canada of +Baeocera inexspectata +. + + + + +Collection and habitat data. + +Baeocera inexspectata +adults were sifted from moss and leaf litter in a mature eastern white cedar ( +Thuja occidentalis +L.) swamp/forest and in a mature red spruce ( +Picea rubens +Sarg.) and red maple ( +Acer rubrum +L.) forest. Adults were captured during May and June. Nothing was previously known about the habitat associations of this species. + + + +Distribution in Canada and Alaska. + +SK, NB ( + +Loebl +and Stephan 1993 + +). Additional sampling in appropriate habitats will probably show this species occurs in intervening areas between New Brunswick and Saskatchewan. + + + + \ No newline at end of file diff --git a/data/38/0C/B7/380CB73B633250B1AC2FEFEC2CAE5E22.xml b/data/38/0C/B7/380CB73B633250B1AC2FEFEC2CAE5E22.xml new file mode 100644 index 00000000000..64154b4d65e --- /dev/null +++ b/data/38/0C/B7/380CB73B633250B1AC2FEFEC2CAE5E22.xml @@ -0,0 +1,318 @@ + + + +The tiger beetles (Coleoptera, Carabidae, Cicindelinae) of Israel and adjacent lands + + + +Author + +Matalin, Andrey V. +Education-Scientific Centre Ecology & Biodiversity, Moscow State Pedagogical University, Moscow 129164, Russia & Department of Biology, Russian National Research Medical University named after N. I. Pirogov, Moscow 117997, Russia +andrei-matalin@yandex.ru + + + +Author + +Chikatunov, Vladimir I. +Department of Zoology, Tel-Aviv University, Tel Aviv 69978, Israel + +text + + +ZooKeys + + +2016 + +2016-04-08 + + +578 + + +115 +160 + + + + +http://dx.doi.org/10.3897/zookeys.578.7383 + +journal article +http://dx.doi.org/10.3897/zookeys.578.7383 +1313-2970-578-115 +A1A7FC2B0E1D4BC88AE430CC9478DF7B +DA5CFFFFFFCE6A62FF8E5903FF8BF778 +579354 + + + + +Calomera aulica aulica (Dejean, 1831) + + + +General distribution. + +Europe +Greece; +Asia +Lebanon, Israel, Jordan, Syria, Egypt (Sinai), Saudi Arabia, Arab Emirates, Oman, Yemen, Bahrain, Iran, Iraq, Pakistan; +Africa +: Cape Verde Islands, Senegal, Guinea Bissau, Mauritania, Morocco, Tunisia, Algeria, Libya, Sudan, Chad, Egypt, Somalia, Eritrea, Djibouti. + + + +References. + +Israel +- +Bodenheimer 1937 +: 108 (as + +Cicindela + +); +Valdenberg 1983 +: 43, 46 (as + +Cicindela + +), +1985 +: 37 (as + +Cicindela + +); +Cassola 1985 +: 56 (as + +Lophyridia + +); +Nussbaum 1987 +: 9-10 (as + +Cicindela + +); +Wiesner 1992 +: 151 (as + +Lophyridia + +); +Puchkov and Matalin 2003 +: 99; +Rittner 2003 +(as + +Lophyridia + +); +Ptashkovsky 2009 +: 8-9 (as + +Lophyra + +); +Egypt (Sinai) +- +Horn 1931 +: 162 (as + +Cicindela + +); +Alfieri 1976 +: 1 (as + +Cicindela + +); Cassola 1984: 56 (as + +Lophyridia + +); +Nussbaum 1987 +: 9-10 (as + +Cicindela + +); +Wiesner 1992 +: 151 (as + +Lophyridia + +); +Werner 2000 +: 98 (as + +Lophyridia + +); +El-Moursy et al. 2001 +: 66 (as + +Cicindela + +); +Abdel-Dayem et al. 2003 +: 205 (as + +Lophyridia + +); +Puchkov and Matalin 2003 +: 103; +Abdel-Dayem 2004 +: 74 (as + +Lophyridia + +). + + + +Distribution + +(Figs +1 +, +2 +). +Israel (including State of Palestine), Jordan Valley +: +Zor Deir Shaman +, 15.III.2005, I. Zonstein - 1♀; +Gesher +, 17.VIII.1939, H. Bytinski-Salz 1♂ (both TAU); +Kinneret zone +(after +Nussbaum 1987 +); +Dead Sea Area +: + +Ne'ot +HaKikkar + +, 7.V.1980, leg. A. Valdenberg 5♂♂ 7♀♀; 16.VII.1999, 13.VIII.1999, +11 +.IX.1999, and 12.XII. 1999, light trap BL, leg. I. Yarom & V. Kravchenko 2♂♂ 7♀♀; +Sedom +, 15.VIII.1957, leg. J. Wahrman 1♂ 2♀♀ (all TAU); ' +En Gedi +, 19-29.V.1989, leg. G. +Mueler +1♀; +Qalya +, 28.VIII.1986, 28.6.1987, leg. Y. Nussbaum 2♂♂ (both cJW); ' +Enot Qane +(after +Nussbaum 1987 +); +Arava Valley +: + +Be'er +Ora + +, 3.IV.1997, leg. V. Chikatunov 3♂♂ 1♀; ' +En 'Iddan +, 15.VII.1999, leg. I. Yarom & V. Kravchenko 1♂ 1♀ (all TAU). + + + +Figure 1. +Distribution of + +Calomera aulica aulica + +in Israel, Palestine and border areas of Jordan (open circles records before year 1949, half-solid circles records between years 1950-1999, solid circles records after year 2000; map source Eric Gaba Wikimedia Commons user: Sting and Wikimedia Commons user: NordNordWest, URL https://upload.wikimedia.org/wikipedia/commons/7/7c/Israel_relief_location_map.jpg) + + + + +Figure 2. +Distribution of + +Calomera aulica aulica + +(red circles) and + +Calomera littoralis aulicoides + +(blue rhombs) in Sinai Peninsula, Egypt (open symbols records before year 1949, half-solid symbols between years 1950-1999, solid symbols records after year 2000; URL map source https://upload.wikimedia.org/wikipedia/commons/5/59/Sinai_relief_location_map.svg). + + + + +Jordan, +Ma'Daba + +: +Callirhoe +, 7.VI.1942, leg. H. Bytinski-Salz 2♀ (TAU). + + +Egypt (Sinai), Northern Sinai +: +Sabkhat al Bardawil +, 25.VIII.1967, leg. I. Margalit 3♀♀; 24.VIII.1979, leg. A. Valdenberg 1♂ 2♀♀ (TAU); +Ismailia +(after +Alfieri 1976 +); +Zaranik Protectorate +(after +El-Moursy et al. 2001 +; +Abdel-Dayem et al. 2003 +; +Abdel-Dayem 2004 +); +Sinai Mountains +: +20 km NE of Dahab +, saline land, 4.VIII.2008, leg. A. Sokolov 4♂♂5♀♀ (MPU); +Southwestern Sinai +: +Suez +- 1♂ (ZMUM); +Nabeq +, 17.VIII.1971, leg. J. Kugler 1♂ 2♀♀; 8.V.1980, leg. A. Valdenberg 4♂♂ 6♀♀; +Ras al Tantur +, 5.VII.1957, leg. Ch. Lewinsohn 2♂♂ 1♀, 17.VIII.1971, leg. M. Kaplan -1♀ (all TAU); +15 km W Ofira +, Golf v. Elat, +Strasse +von Tiran, 3.IV.1981, leg. G. Gerdes 1♂ (cJW); +Wadi Gharandal +, 20.V.1969, leg. Tsabar 1♂ (TAU); +Abu Zenima +, +Wadi Tayebeh +(both after +Alfieri 1976 +); +El Tor +(after +Alfieri 1976 +; +Abdel-Dayem et al. 2003 +; +Abdel-Dayem 2004 +); +Ras Muhammad +(after +Nussbaum 1987 +). + + + + \ No newline at end of file diff --git a/data/38/0C/FF/380CFF4A965415D4BEBC16736AD7C43D.xml b/data/38/0C/FF/380CFF4A965415D4BEBC16736AD7C43D.xml new file mode 100644 index 00000000000..2ebbd85ac9c --- /dev/null +++ b/data/38/0C/FF/380CFF4A965415D4BEBC16736AD7C43D.xml @@ -0,0 +1,83 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828--9042 + + + + +Tranosemella praerogator (Linnaeus, 1758) + + + + +Ichneumon praerogator +Linnaeus, 1758 + + +chrysogaster +(Gmelin, 1790, +Ichneumon +) preocc. + + +mandibulator +(Thunberg, 1824, +Ichneumon +) + + +interrupta +(Holmgren, 1858, +Limneria +) + + +laticrus +(Thomson, 1887, +Angitia +) + + + +Distribution +England, Scotland, Wales, Ireland, Isle of Man + + +Notes + +some distribution data from +Shaw (1981) + + + + \ No newline at end of file diff --git a/data/38/0D/16/380D1646B29162C08A473408C403E143.xml b/data/38/0D/16/380D1646B29162C08A473408C403E143.xml new file mode 100644 index 00000000000..0145ca29530 --- /dev/null +++ b/data/38/0D/16/380D1646B29162C08A473408C403E143.xml @@ -0,0 +1,84 @@ + + + +Polychaetes of Greece: an updated and annotated checklist + + + +Author + +Faulwetter, Sarah + + + +Author + +Simboura, Nomiki + + + +Author + +Katsiaras, Nikolaos + + + +Author + +Chatzigeorgiou, Giorgos + + + +Author + +Arvanitidis, Christos + +text + + +Biodiversity Data Journal + + +2017 + +5 + + +20997 +20997 + + + + +http://dx.doi.org/10.3897/BDJ.5.e20997 + +journal article +http://dx.doi.org/10.3897/BDJ.5.e20997 +1314-2828--20997 + + + + +Harmothoe extenuata (Grube, 1840) + + + + +Harmothoe extenuata +(Grube, 1840) | +Lagisca extenuata +(Grube, 1840) + + + +Notes + +Easily confused with other species of +Harmothoe +, literature records from the Mediterranean and North-East Atlantic should be treated with care ( +Barnich and Fiege 2000a +). + + + + \ No newline at end of file diff --git a/data/38/0D/87/380D87C768711C415E8FFAB4FBDEF9B8.xml b/data/38/0D/87/380D87C768711C415E8FFAB4FBDEF9B8.xml new file mode 100644 index 00000000000..2d452226429 --- /dev/null +++ b/data/38/0D/87/380D87C768711C415E8FFAB4FBDEF9B8.xml @@ -0,0 +1,123 @@ + + + +Records and descriptions of some Aphelinidae (Hymenoptera: Chalcidoidea) from India + + + +Author + +Hayat, Mohammad + +text + + +Zootaxa + + +2012 + +3521 + + +39 +50 + + + +journal article +10.5281/zenodo.212460 +31cf3018-bcd9-4bd8-bfe2-b440e27a1f0f +1175-5326 +212460 + + + + + + + +Coccophagus longifasciatus +Howard + + + + + + + + + +Coccophagus longifasciatus + +Howard, 1907 +: 80 + + +, female. +Ceylon +[= +Sri Lanka +], Manaar (USNM), +syntypes +examined by + +Hayat (1998: 155) + +. + +Compere, 1931 +: 74 + +, notes and figures based upon specimens from +China +. + +Hayat & Khan, 2010 +: 12 + +, female, figures. +India +record. + + + + + +Material examined. +INDIA +: KARNATAKA: Mandya, Srirangapatna, +1 female +, +4.i.2012 +, Coll. FR Khan ( +ZDAMU +). +PUDUCHERRY +: +Mahe +, +1 female +(on slide under 4 coverslips), +8.i.2012 +, Coll. FR Khan ( +ZDAMU +). + + + + +Comments. +This species was recorded from +India +by +Hayat & Khan (2010) +based on a female from Odisha. It is recorded here from Karnataka State and +Mahe +(Union Territory of +Puducherry +). + + + + \ No newline at end of file diff --git a/data/38/0D/87/380D87C768711C415E8FFC3BFB91FB5B.xml b/data/38/0D/87/380D87C768711C415E8FFC3BFB91FB5B.xml new file mode 100644 index 00000000000..2968284ef43 --- /dev/null +++ b/data/38/0D/87/380D87C768711C415E8FFC3BFB91FB5B.xml @@ -0,0 +1,103 @@ + + + +Records and descriptions of some Aphelinidae (Hymenoptera: Chalcidoidea) from India + + + +Author + +Hayat, Mohammad + +text + + +Zootaxa + + +2012 + +3521 + + +39 +50 + + + +journal article +10.5281/zenodo.212460 +31cf3018-bcd9-4bd8-bfe2-b440e27a1f0f +1175-5326 +212460 + + + + + + + +Coccophagus fumadus +Hayat + + + + + + + +Coccophagus fumadus +Hayat + +, in + +Hayat & Khan, 2010 +: 11 + +, female. +India +, Orissa [= Odisha], Puri, Matia Pada (NPC). + + + + + +Material examined. +INDIA +: +PUDUCHERRY +[formerly, +Pondicherry +]: +Mahe +, +2 females +(one on slide under 4 coverslips), +8.i.2012 +, Coll. FR Khan ( +ZDAMU +). KERALA: Thatidikkara, +1 female +, +8.i.2012 +, Coll. FR Khan; Ernakulam, Cherai, +1 female +, +11.i.2012 +, Coll. FR Khan ( +ZDAMU +). + + + + +Comments. +This species was recently described from a single female collected in the Orissa (now Odisha) State. It is here recorded from Kerala State and +Mahe +(Union Territory of +Puducherry +). + + + + \ No newline at end of file diff --git a/data/38/0D/87/380D87C768711C4F5E8FF917FDABFC01.xml b/data/38/0D/87/380D87C768711C4F5E8FF917FDABFC01.xml new file mode 100644 index 00000000000..ab27003f6c0 --- /dev/null +++ b/data/38/0D/87/380D87C768711C4F5E8FF917FDABFC01.xml @@ -0,0 +1,224 @@ + + + +Records and descriptions of some Aphelinidae (Hymenoptera: Chalcidoidea) from India + + + +Author + +Hayat, Mohammad + +text + + +Zootaxa + + +2012 + +3521 + + +39 +50 + + + +journal article +10.5281/zenodo.212460 +31cf3018-bcd9-4bd8-bfe2-b440e27a1f0f +1175-5326 +212460 + + + + + + + +Coccophagus zebratus +Howard + + + + + +( +Figs 12–15 +) + + + + + + + + + + + + + + + + + +
+ +Coccophagus +zebratus +Howard, 1907: 81 + +, +female. Ceylon [= Sri Lanka], Punduloya [= Pundaluoya],(USNM), syntypes
examined by Hayat (1992). Compere,1931: 16, 64–66, female, redescription, figures, key. Hayat,1992: 112, figures,
+placed in + +zebratus + +species group. +
+
+ + +Redescription. +Female. +Length, +0.84 mm +(excluding exserted part of ovipositor, +0.07 mm +). Head white; frontovertex pale brownish yellow; malar sulcus black; occiput brown. Mandible in apical half reddish brown. Antenna ( +Fig. 14 +) with radical and scape white, scape with dark brown streaks along distal half of ventral margin on inner surface and in distal two-thirds to three-fourths on outer surface; pedicel dark brown with white dorsal surface; F1, F2 and clava dark brown; F3 pale yellow to white. Mesosoma ( +Fig. 12 +) white, except as follows: pronotum with a dark brown transverse streak anterior to collar and a black spot at each posterolateral corner; mid lobe of the mesoscutum with a brown patch in anterior half, and two pale brown oblique streaks on sides beginning from posterior margin; each side lobe with a pale brown streak; axilla mostly dark brown; scutellum with two dark brown rectangular patches in posterior two-thirds; propodeum dark brown. Fore wing hyaline with very light infuscation on disc ( +Fig. 15 +). +Hind +wing hyaline. Legs, including coxae, white; mid and hind tibiae in about basal third pale brown; mid and hind basitarsi, and last segments of all tarsi brown. Metasoma ( +Fig. 12 +) white, with transverse, dark brown bands on each of TI–TV; TVI dark brown with white lateral areas; TVII dark brown with lateral areas and apex white; ovipositor sheaths dark brown. + + + +FIGURES 12–15. + +Coccophagus zebratus +Howard + +, female: 12, mesosoma and metasoma; 13, head, frontal; 14, antenna; 15, fore wing. + + + +Head ( +Fig. 13 +). Head flattened, in frontal view, 1.4× as broad as high; frontovertex width, at level of anterior ocellus, 0.52× head width; frontovertex with moderately long black setae; malar space and clypeus with hyaline setae; eyes setose, setae hyaline, and each seta shorter than a facet. Antenna as in +Fig. 14 +; F1 slightly shorter than pedicel and F2; clava subequal in length to funicle. +Relative measurements +—frontal width of head, 32.5; frontal height of head, 23; frontovertex width, 17; eye height, 17; malar space, 8; antennal scape length, 9. + + +Mesosoma ( +Fig. 12 +). Setae as follows: pronotal collar with 6 or 7 + 6 or 7 setae, in addition to several setae anteriorly on disc, and a long seta at each posterolateral corner; mid lobe of mesoscutum with 42 setae; each side lobe with 3 setae; each axilla with 3 setae; scutellum with 6 setae; propodeum with 2 setae on each side distal to spiracle. Fore wing ( +Fig. 15 +) 3.26× as long as broad; venation about 0.7× wing length; costal cell slightly shorter than marginal vein (20:21.5); postmarginal vein about one-third length of stigmal vein. +Hind +wing 6.6× as long as broad; marginal fringe 0.58× wing width. +Relative measurements +—mesosoma length, 34; mesoscutum length, 13; scutellum length, 8.5; propodeum median length, 5; fore wing length (width), 62 (19); hind wing length (width), 56.5 (8.5); marginal fringe length, 5. + + +Metasoma. Metasoma, measured on card, 1.35× as long as mesosoma, but after clearing and mounting on slide ( +Fig. 12 +), measures 1.85× as long as mesosoma; exserted part of ovipositor sheaths 0.15× gaster length; setae on tergites as follows: TI–TIII each with 2+2; TIV with 4+4; TV with 6+1+1+6; TVI with 2+1+1+2, the seta adjacent to each cercal plate longest; TVII with several setae of which +4 in +posterior line nearly twice as long as other setae; ovipositor with second valvifer 2.63× as long as third valvula. +Relative measurements +—ovipositor length, 40; third valvula length, 11; mid tibia length, 17.5; mid basitarsus length, 5.25; mid tibial spur length, 5. + + +Male. +Unknown. + + + + +Material examined. +INDIA +: KERALA: +Calicut +, +IISR +Campus, +1 female +(on slide under 4 coverslips), +7.i.2012 +, Coll. FR Khan ( +ZDAMU +). + + +Host. +Unknown for Indian specimen. + +Aclerda distorta +Green + +( +Hemiptera +: +Aclerdidae +) in +Sri Lanka +( +Howard, 1907 +). + + + + +Distribution. +Sri Lanka +; +India +: Kerala (present record). + + + + +Comments. + +Coccophagus zebratus + +and + +C. planus +( +Sugonjaev 1969 +) + +were placed in a separate species group, the + +zebratus + +-group, by +Hayat (1992) +. These two species are very similar in body colour and other structural characters, but + +C. zebratus + +differs from + +C. planus + +in having F3 pale yellow to white, whereas in + +C. planus + +F3 is blackish similar to F1, F2 and the clava. + + +
+
\ No newline at end of file diff --git a/data/38/0D/87/380D87C768731C415E8FFCD9FA6FFD02.xml b/data/38/0D/87/380D87C768731C415E8FFCD9FA6FFD02.xml new file mode 100644 index 00000000000..464ae3ccd84 --- /dev/null +++ b/data/38/0D/87/380D87C768731C415E8FFCD9FA6FFD02.xml @@ -0,0 +1,266 @@ + + + +Records and descriptions of some Aphelinidae (Hymenoptera: Chalcidoidea) from India + + + +Author + +Hayat, Mohammad + +text + + +Zootaxa + + +2012 + +3521 + + +39 +50 + + + +journal article +10.5281/zenodo.212460 +31cf3018-bcd9-4bd8-bfe2-b440e27a1f0f +1175-5326 +212460 + + + + + + + +Proaphelinoides assamensis +Hayat + +, +sp. nov. + + + + +( +Figs 6–11 +) + + + + + + +Proaphelinoides australis +Girault + +: + +Hayat & Zeya, 1993 +: 65 + +, female, +India +, Assam. + +Hayat, 1998 +: 76 + +, female, description, figures 143–147. Misidentification. + + + + + +Female +( +holotype +). Length of mesosoma plus metasoma, +1.15 mm +. Head pale yellow, a large patch on occiput brown. Mandible reddish brown in apical half. Antennal radicle and scape pale yellow; pedicel and flagellum brownish yellow. Mesosoma pale yellow to white; posterior margin of scutellum and sides of propodeum brown. Fore wing hyaline with two infuscated patches, one lightly infuscate patch below proximal half of marginal vein and another distinct patch below distal end of marginal vein, extending onto disc as in +Fig. 9 +. +Hind +wing mostly hyaline, but with distal half lightly infuscated ( +Fig. 10 +). Legs pale yellow with some brownish suffusions especially on hind coxa and hind femur. Metasoma ( +Fig. 11 +) dark brown; petiole and TVIII white; TI and TII white dorsally and pale brown laterally. + + +Head ( +Fig. 6 +). It is not possible to measure head dimensions accurately as it is distorted due to pressure from the coverslip, and the vertex on right side is partially damaged, but width of frontovertex at level of anterior ocellus appears about 0.46× head width; antennal toruli situated slightly below a line drawn between lower margin of eyes, and separated from mouth margin by a distance equal to 1.42× length of a torulus; intertorular space and malar space with fine, short, hyaline setae; a line of 5 long setae along each eye margin; vertex with long, dark brown [now appear pale brown] setae; occiput with several dark brown setae, of which 2 setae are very long and 4 setae are each about half the length of the longer seta (setae on occiput are shown in broken lines in +Fig. 6 +); eyes setose, setae hyaline and each about as long as a facet. Antenna ( +Fig. 7 +) with scape 4.48× as long as broad; pedicel 1.65× as long as broad, and as long as F2 and F3 combined; F1 slightly longer than F2; F3 quadrate (length measured along ventral margin); clava slightly longer than pedicel and F1–F3 combined (12.5:11.25). + + +Mesosoma ( +Fig. 8 +; also +Hayat, 1998 +: fig. 147). Pronotum slightly less than half length of mesoscutum, the latter subequal in length to scutellum; scutellum 1.67× as broad as long; metanotum very narrow, one-seventh propodeum length; propodeum 0.5× scutellum length; setae on tergites as follows: pronotal collar with 3+3 setae, and a long seta at each posterolateral corner; mid lobe of the mesoscutum with 6+6 setae, of which 1 seta at each anterolateral corner and 2 posterior setae are longer; each side lobe with 2 setae; each axilla with 1 long seta; scutellum with 2+2 long setae; propodeum with 3 setae on each side, 1 relatively thick seta near anterior margin of spiracle and 2 setae distal to spiracle. Fore wing ( +Fig. 9 +; also +Hayat, 1998 +: fig. 145) 2.57× as long as broad; venation extending 0.68× wing length; costal cell 0.61× length of marginal vein, and with 1 seta distally on dorsal surface; submarginal vein with 2 setae, distal seta nearly 2× as long as proximal seta; parastigma with 1 long seta; marginal vein with 11 setae; linea calva proximally bordered by 2 lines of setae which become 3 lines in posterior third; linea calva closed posteriorly by 1 line of setae; a bunch of 17–20 dark setae below proximal half of marginal vein, and 2 setae in basal cell near proximal end of parastigma. +Hind +wing ( +Fig. 10 +) 4.36× as long as broad; longest setae of marginal fringe (at basal third of posterior margin) 0.42× wing width. +Relative measurement +—mesosoma length, 42; mesoscutum length, 13.5; scutellum length (width), 14 (23.5); metanotum length, 1; propodeum length, 7; fore wing length (width), 90 (35); costal cell length, 21; marginal vein length, 34; hind wing length (width), 83 (19); marginal fringe length, 8. + + + +FIGURES 6–11. + +Proaphelinoides assamensis +Hayat + +, + +sp. nov. +, + +female: 6, head, frontal; 7, antenna; 8, mesosoma; 9, fore wing; 10, hind wing; 11, metasoma. + + + +Metasoma ( +Fig. 11 +) 1.76× as long as mesosoma; ovipositor originates from level of posterior half of TI of gaster; ovipositor 2.46× as long as mid tibia; second valvifer 2.83× as long as third valvula; TI–TVIII with setae as follows: TI–TIII, 1+1 each; TIV, 3+2; TV, 1+6+1; TVI, +8 in +line near anterior margin; TVII, no setae; TVIII with numerous setae, illustrated by +Hayat (1998: fig. 146) +. +Relative measurements +— metasoma length, 74; ovipositor length, 69; third valvula length, 18; mid tibia length, 28; mid basitarsus length, 12; mid tibial spur length, 9.5. + + +Male. +Unknown. + + + + +Material examined. +Holotype +( +ZDAMU +, Registration No. HYM. +CH +.652), female (on slide under 4 coverslips), labelled in black ink in Hayat’s handwriting: “ +INDIA +: Assam, Silchar, +9.xi.1989 +Coll. M.C. Basha +Proaphelinoides +”, “ + +Proaphelinoides australis Grlt. Det. +M. Hayat 1992 + +”, and a printed label, “ +HOLOTYPE +[in red], female + +Proaphelinoides assamensis +Hayat + +, +sp. nov. +”. + + +Host. +Unknown. + + + + +Distribution. +India +: Assam. + + + + +Etymology. +The species name is derived from the name of the Indian State (Assam) from where the +holotype +was collected. + + + + +Comments. +The +holotype +of the new species described here as + +Proaphelinoides assamensis + +was misidentified as + +P. australis +Girault (1922a) + +by +Hayat & Zeya (1993) +, and later redescribed and illustrated by +Hayat (1998: figs 143–147) +. It differs from + +P. australis + +in the following characters: antenna with F3 quadrate (if measured along ventral margin) to 1.25× as long as broad (if measured along dorsal margin); linea calva of fore wing proximally bordered by 2 lines of setae which become 3 lines in posterior third; TVIII of gaster about as long as broad (width measured between cercal plates); ovipositor 2.46× as long as mid tibia; and second valvifer 2.83× as long as third valvula. In + +P +. +australis + +: F3 1.2× (measured along ventral length) to 1.4× (measured along dorsal length) as long as broad; linea calva of fore wing proximally bordered by a single line of setae; TVIII of gaster 1.88× as long as broad; ovipositor 2.61× as long as mid tibia; and second valvifer 2.95× as long as third valvula. Measurements based on figures drawn from +holotype +( +Hayat, 1985 +). + + +The recent key to the world species of + +Proaphelinoides + +given by +Menakadevi & Manickavasagam (2012) +may be modified as follows to accommodate +P. a s s a m e n s i s +: + +2. Fore wing with linea calva proximally bordered by at least 1 line of setae........................................ 2a - Fore wing with linea calva proximally without a setal line..................................................... 4 2a. Linea calva proximally bordered by 2 lines of setae which become 3 lines in posterior third (F3 quadrate to slightly longer than + +broad if measured along dorsal length; fore wing with tuft of 17–20 black setae below proximal half of marginal vein) ( +India +) + + +............................................................................. + +P. assamensis +Hayat + +, + +sp. nov. + +- Linea calva proximally bordered by a single line of setae...................................................... 3 + + + + \ No newline at end of file diff --git a/data/38/0D/87/380D87C768761C435E8FFED0FADAFCF9.xml b/data/38/0D/87/380D87C768761C435E8FFED0FADAFCF9.xml new file mode 100644 index 00000000000..8d3f82a68c3 --- /dev/null +++ b/data/38/0D/87/380D87C768761C435E8FFED0FADAFCF9.xml @@ -0,0 +1,305 @@ + + + +Records and descriptions of some Aphelinidae (Hymenoptera: Chalcidoidea) from India + + + +Author + +Hayat, Mohammad + +text + + +Zootaxa + + +2012 + +3521 + + +39 +50 + + + +journal article +10.5281/zenodo.212460 +31cf3018-bcd9-4bd8-bfe2-b440e27a1f0f +1175-5326 +212460 + + + + + + + +Centrodora flemingiae +Hayat + +, +sp. nov. + + + + +( +Figs 1–5 +) + + + + +Female. +Length +1.02–1.15 mm +( +holotype +, +1.15 mm +). Head with vertex brownish yellow; frons brown; facial region pale brown; malar space brown; occiput white. Mandible reddish brown. Antenna with scape pale brown; pedicel and flagellum dark brown. Pronotum pale brownish yellow, collar pale brown; mid lobe of mesoscutum yellowish brown; side lobes yellow; axillae largely dark brown; scutellum yellow to brownish yellow, with posterior margin sometimes brown; a pale mid-longitudinal line on mid lobe and scutellum present; tegula dark brown; metanotum white with dorsellum brownish yellow; propodeum white with a dark brown patch mesal to each spiracle; prepectus, mesopleuron and metapleuron white, mesopleuron in about anterior third with some pale brown suffusions. Fore wing hyaline, with an infuscated streak below proximal end of marginal vein ( +Fig. 5 +). +Hind +wing hyaline. Legs white except as follows: fore coxa with pale brown suffusions in distal half; fore femur brownish along ventral margin; fore tibia largely brown; fore tarsus brown; mid femur except basal fifth or so pale brown; mid tibia pale brown; mid basitarsus pale brown in about basal two-thirds; hind coxa brown to dark brown with apex white; hind femur dark brown. Gaster ( +Fig. 1 +) with TI, TV–TVII dark brown, TIV with a pale brown cross band; TII and TIII pale yellow; TVIII white. + + +Head ( +Fig. 2 +). Head, in frontal view, 1.09× as broad as high; frontovertex width, at level of anterior ocellus, 0.43× head width; ocellar triangle with apical angle a right angle (90o); posterior ocelli separated from eye margin by a distance about equal to diameter of an ocellus; vertex with raised reticulate sculpture; frons and face with rugose-reticulate sculpture, shallower than on vertex; malar space behind sulcus with elongate reticulate sculpture; setae on frontovertex dark brown to black and bristle-like; 4 long setae in a transverse line on occiput, 2 long setae on occipital margin; other setal arrangement as in +Fig. 2 +; setae on face and malar space short and translucent; eyes with very short, translucent setae. Mandible ( +Fig. 2 +) with 3 teeth, dorsal tooth may appear as a short truncation. Antenna ( +Fig. 3 +) with scape cylindrical, 5.8× as long as broad; pedicel 3.2× as long as broad, about as long as F1 and F2 combined; F1 shortest, with apex oblique (ventral margin longer than dorsal margin), 1.85× as long as broad; F2 2.92× as long as broad, and 1.57× as long as F1; F3 very slightly longer than F2 and 2.68× as long as broad; clava about as long as combined length of F3, F2, and half of F1; F1 and F2 without longitudinal sensilla, F3 with 1 or 2 sensilla, and clava with 6 or 7 sensilla. + + +Mesosoma ( +Figs 1 +, +4 +). Median length of mid lobe of mesoscutum 1.33× as long as median length of scutellum; scutellum slightly broader than long (16:15); dorsellum 0.3× length of scutellum; propodeum 0.46× scutellum length; mesoscutum and scutellum with polygonal reticulate sculpture, appearing raised reticulate in brownish areas; dorsellum with polygonal reticulate sculpture; propodeum medially with elongate reticulate to lineolatereticulate sculpture; setae on pro- and mesothoracic dorsum dark brown to black; pronotal collar with 2 lines of setae on each half of pronotum and a long seta at each posterolateral corner; mid lobe of mesoscutum with 35–40 setae, of which 1 seta on each anterolateral corner and the 2 setae along posterior margin long; each side lobe with 3 setae, rarely 2 setae on one side lobe; tegula with 2 setae; axilla with 1 seta and scutellum with 4 (2+2) long setae; propodeum with 2 short, translucent setae adjacent to outer margin of each spiracle. Fore wing 3.2–3.3× as long as broad; marginal fringe about 0.15× wing width; venation reaching to half length of wing; costal cell usually at least slightly longer than marginal vein, but in one specimen ( +Fig. 5 +) as long as marginal vein; costal cell with 2–4 dark setae distally on dorsal surface, and apparently no setae on ventral surface; 3 setae on submarginal vein, 2 setae on parastigma, and 8 setae on marginal vein; postmarginal vein about half length of stigmal vein; linea calva present, narrow, closed by about 3 lines of setae both anteriorly and posteriorly; speculum present; area below parastigma and submarginal vein setose. +Hind +wing about 5.5× as long as broad; marginal fringe about one-third wing width; disc setose except bare below submarginal vein. Legs long; mid basitarsus half or nearly half length of mid tibia and as long as tarsal segments 2–5 combined. +Relative measurements +( +holotype +)—mesoscutum length, 20; scutellum length (width), 15 (16); dorsellum length, 4.5; propodeum length, 7; fore wing length (width), 96 (29); marginal fringe length, 4.5; hind wing length (width), 80 (14.5); marginal fringe length, 5. + + + +FIGURE 1. + +Centrodora flemingiae +Hayat + +, + +sp. nov. +, + +female, body dorsal. + + + +Metasoma ( +Fig. 1 +). If gaster undistorted, slightly longer than mesosoma (55:53); ovipositor originating from near base of gaster, and very shortly exserted; ovipositor 1.27× as long as mid tibia; third valvula 0.25× second valvifer; setae on tergites as follows: TI–TIV with 2+2 each; TV with a line of 10–12 setae; TVI with two lines of 8 and 8 setae, setae of the posterior line longer; TVII without setae; and TVIII with 7 setae. +Relative measurements +( +holotype +)—ovipositor length, 56; third valvula length, 11.25; mid tibia length, 44; mid basitarsus length, 22.5; mid tibial spur length, 20.5. + + +Male. +Unknown. + + + + +Material examined. +Holotype +( +NPC +, Registration No. 13/6/119/11), female (on slide under two coverslips) labelled “ +INDIA +: JHARKHAND: Ranchi, +22.xii.2011 +, ex eggs on + +Flemingia + +sp. [collector unknown]. +Paratypes +: +3 females +(on 3 slides), with data same as for +holotype +. (One female in +NPC +, Registration No. 13/6/119/12; +2 females +in +ZDAMU +, Registration No. HYM. +CH +.651). + + +Specimens with same data as +holotype +, but not designated as +types +: +3 females +(on 2 slides); one female with both antennae beyond F1 and left side legs missing; one female with metasoma missing; and one female with right wings and all legs missing). + + +Host. +Undetermined eggs on + +Flemingia + +sp. (Leguminosae). + + + + +Distribution. +India +: Jharkhand. + + + + +Etymology. +The species name is derived from the name of the plant on which the host eggs were collected. + + + + +Comments. +It should be noted that in at least the Indian species of + +Centrodora +Förster + +, + +Proaphelinoides +Girault + +and + +Coccophagoides +Girault + +, a narrow sclerite connected or approximated laterally of the outer plates of the ovipositor is present. This sclerite actually represents TVII of the gaster, and the apparent last tergite is the eighth tergite (TVIII). + + + +FIGURES 2–5. + +Centrodora flemingiae +Hayat + +, + +sp. nov. +, + +female: 2, head, frontal; 3, antenna; 4, mesosoma; 5, fore wing, basal half. + + + +The new species of + +Centrodora +Förster + +described here is unique in having 35–40 setae on the mid lobe of the mesoscutum. In nearly all other described species of this genus the number of setae on the mid lobe of the mesoscutum varies from 4 to 12 or rarely 14, but one species, + +C. mireyae +( +De Santis 1981 +) + +, has 14–19 setae, and two other species, + +C. damoni + +( +Girault 1922b +; +holotype +examined by +Hayat & Fatima 1990 +) and + +C. homopterae +( +Risbec 1951 +) + +each have 22 setae ( +Ferrière 1965 +; +Hayat 1983 +, +1998 +, 2010—to cite just 4 references). + + +The new species appears similar to + +C. homopterae + +(from +Senegal +; based on the original description and figures given by +Risbec 1951 +), but differs in several characters including relative dimensions of the antennal segments. In + +C. flemingiae + +: antenna with scape 1.8× as long as pedicel; pedicel 2.46× as long as F1; F2 1.57× as long as F1 and 0.95× F3; clava about as long as funicle; mid lobe of the mesoscutum with 35–40 setae; fore wing at least 3.2× as long as broad, and with an infuscated streak below proximal end of marginal vein; and body colour partly pale yellow to dark brown, with TI, TV–TVII dark brown, TIV with a pale brown cross band, TII and TIII pale yellow, and TVIII white. In + +C. homopterae + +: antenna with scape 3× as long as pedicel; pedicel 2.75× as long as F1; F2 2× as long as F1, and subequal in length to F3; clava slightly longer than funicle (12:10); mid lobe of mesoscutum with 22 setae; fore wing 3× as long as broad, and hyaline; and body entirely pale yellow, the face a little darker. + + +In +1981 I +saw in the BMNH an undescribed species of + +Centrodora + +with numerous setae on the mid lobe of the mesoscutum, but otherwise is quite different from the new species. The specimens were from +Trinidad +( +St. Vincent +) and +Brazil +. + + +All the described Indian species of + +Centrodora + +( +Hayat 1998 +, 2010) are quite different from the new species not only in having only 4–12 setae on the mid lobe of the mesoscutum, but also in the relative dimensions of the flagellar segments, especially in having F2 at most two-thirds the length of F3 and usually much shorter. + + + + \ No newline at end of file diff --git a/data/38/0D/87/380D87C7687D1C4D5E8FFE99FCD8FCC1.xml b/data/38/0D/87/380D87C7687D1C4D5E8FFE99FCD8FCC1.xml new file mode 100644 index 00000000000..731c8cd3208 --- /dev/null +++ b/data/38/0D/87/380D87C7687D1C4D5E8FFE99FCD8FCC1.xml @@ -0,0 +1,135 @@ + + + +Records and descriptions of some Aphelinidae (Hymenoptera: Chalcidoidea) from India + + + +Author + +Hayat, Mohammad + +text + + +Zootaxa + + +2012 + +3521 + + +39 +50 + + + +journal article +10.5281/zenodo.212460 +31cf3018-bcd9-4bd8-bfe2-b440e27a1f0f +1175-5326 +212460 + + + + + + + +Eriaphytis chackoi +Subba Rao + + + + + +( +Figs 22–24 +) + + + + + + +Eriaphytis chackoi + +Subba Rao, 1980 +: 44 + + +–45, female. +India +, Karnataka, Pulney Hill (BMNH). + +Hayat, 1998 +: 117 + +, female, redescription, figures. + + + + + +Material examined. +INDIA +: KARNATAKA: Bengaluru [formerly, Bangalore], Hebbal, +68 females +(on 4 cards; +4 females +on two slides), +20.iv.2009 +, ex + +Ceroplastes + +sp., Coll. K. Veenakumari (Collection No. A.573) ( +31 females +in +ZDAMU +; +37 females +returned to Dr. Veenakumari in +NBAII +). + + + + +Comments. +This species has not been reported since its original description based on +7 females +( +holotype +and 6 +paratypes +) reared from + +Vinsonia stellifera +Westwood + +( +Hemiptera +: +Coccidae +). The above listed specimens, reared from a species of + +Ceroplastes +Gray + +( +Hemiptera +: +Coccidae +), were received from Dr. K. Veenakumari of the NBAII, Bengaluru. Because this beautiful species was described in detail with illustrations by +Subba Rao (1980) +and later redescribed and illustrated by +Hayat (1998) +, I do not redescribe the species but for the first time provide photographs of the head, body and fore wing ( +Figs 22–24 +). + + + + \ No newline at end of file diff --git a/data/38/0D/87/380D87C7687F1C4D5E8FFB81FB1DFF39.xml b/data/38/0D/87/380D87C7687F1C4D5E8FFB81FB1DFF39.xml new file mode 100644 index 00000000000..1df9b723064 --- /dev/null +++ b/data/38/0D/87/380D87C7687F1C4D5E8FFB81FB1DFF39.xml @@ -0,0 +1,212 @@ + + + +Records and descriptions of some Aphelinidae (Hymenoptera: Chalcidoidea) from India + + + +Author + +Hayat, Mohammad + +text + + +Zootaxa + + +2012 + +3521 + + +39 +50 + + + +journal article +10.5281/zenodo.212460 +31cf3018-bcd9-4bd8-bfe2-b440e27a1f0f +1175-5326 +212460 + + + + + + + +Paraphytis transversa +(Huang) + + + + + +( +Figs 16–21 +) + + + + + + +Aphytis transversus + +Huang, 1994 +: 47 + + +, 53–55, female. +China +, Fujian, Fuzhou, Jinshan. + +Paraphytis transversa +(Huang) + +: + +Kim & Heraty, 2012 +: 547 + +. + + + + + +Redescription. +Female. +Length, +0.9 mm +(exserted part of ovipositor, +0.05 mm +) Head ( +Fig. 16 +) white; malar sulcus dark brown; mouth margin and behind malar space brown; occiput with a dark brown bar on each side of foramen magnum. Mandible dark brown in apical half. Antenna ( +Fig. 18 +) white; scape with two oblique brown stripes beginning from near apex of ventral margin, one a complete stripe on inner surface reaching to middle of dorsal margin, and the other an incomplete stripe on outer surface reaching to half scape width; ventral half of pedicel brown; F1 and F2 dark brown; clava in about basal third brown, and light brown in about apical third. Mesosoma ( +Fig. 19 +) white; each pronotal plate with a brown stripe and a dark brown dot at posterolateral corner; each side lobe with posterior narrow part pale brown; each axilla on inner third brown; scutellum with a brown subtriangular area in middle; dorsellum pale brown; propodeum in lateral third brown and with a dark brown cross band in posterior half. Fore wing infuscation as in +Fig. 21 +; the hyaline bands distal to venation with transparent setae; otherwise setae all dark brown. +Hind +wing hyaline, but lightly infuscate behind marginal vein. Legs, including fore and mid coxae, white except as follows: fore leg—trochanter brown, tibia with two brown rings, one sub-basal and the other apical, and fifth tarsal segment pale brown; mid leg—femur with a dark brown streak in basal half along upper surface, tibia with distal two-fifths brown, and fifth tarsal segment pale brown; hind leg—coxa brown, femur in basal third along upper margin and about apical third brownish, tibia largely brown, and fifth tarsal segment pale brown. Petiole and TI–TVI dark brown; TVII white; ovipositor sheaths (= third valvulae) dark brown. + + +Head ( +Figs 16, 17 +). Dorsal length 0.46× mesosoma length; setae largely bristle-like and dark brown: frontovertex with 2 short setae slightly behind posterior ocelli, and 3 pairs of setae in front of anterior ocellus; 4 pairs of setae above face, one pair along each eye margin and two pairs medially; occiput with 5 long bristles and two pairs of short setae. Eyes densely setose, setae dark brown, each seta about as long as a facet. Mandible with two pointed teeth and a dorsal rounded tooth. Antenna as in +Fig. 18 +. + + + +FIGURES 16–21. + +Paraphytis transversa +(Huang) + +, female: 16, head, dorsofrontal; 17, head, camera lucida drawing, showing dorsal setae on right half and occipital setae on left half; 18, antenna; 19, mesosoma and metasoma; 20, part of propodeum showing sculpture, crenulae and scale-like seta anterior to spiracle; 21, fore wing. + + + +Mesosoma ( +Fig. 19 +). Setae as follows: each pronotal plate with 4 or 5 setae along collar, and a long seta at posterolateral corner; mid lobe of mesoscutum with 8 setae, the anterior pair of setae shorter; each side lobe with 1 short and 1 long setae; each axilla with 1 seta; scutellum with 4 setae; propodeum with 3 fine setae outside each spiracle and 1 scale-like seta anterior to each spiracle. Sculpture of propodeum and propodeal crenulae illustrated in +Fig. 20 +. Fore wing ( +Fig. 21 +) 2.6× as long as broad; marginal fringe 0.14× wing width. +Hind +wing 5.3× as long as broad; marginal fringe 0.6× wing width. + + +Metasoma ( +Fig. 19 +). Metasoma 1.14× as long as mesosoma; setae on each half of tergites 1–6 as follows: 4+1; 5+1; 5–6+1; 6–7+1; 4+1+1; 1+6–7; TVII with about 24 setae, one seta at each lateral margin longer than other setae. +Relative measurements +(slide)—ovipositor length, 45; third valvula length, 10; mid tibia length, 21.5; mid basitarsus length, 9.5; mid tibial spur length, 8.75. + + +Male. +Unknown. + + + + +Material examined. +INDIA +: KERALA: Malappuram, Kutilamgadi, +1 female +(on slide under 4 coverslips), +9.i.2012 +, Coll. FR Khan ( +ZDAMU +). + + +Hosts. +Unknown. + + + + +Distribution. +China +; +India +: Kerala (present record). + + + + +Comments. +This species, along with others, was recently transferred to the reinstated genus + +Paraphytis +Compere + +by +Kim & Heraty (2012) +. Their decision to remove + +Paraphytis + +from synonymy under + +Aphytis +Howard + +was based on a cladistic analysis of morphological characters. In spite of this, I am not sure whether their action is justified because, except for the undivided mesopleuron, there is no other character to consider + +Paraphytis + +different from + +Aphytis + +. + + +An English translation of the original description of + +Paraphytis transversa + +(in Chinese) was provided by Dr. J. Huang. The Indian specimen agrees fairly well with the description and figures given in +Huang (1994) +, which were based on a single specimen, the +holotype +. There are, however, some slight differences in the Indian specimen as noted below followed in parentheses for the +holotype +of + +P. transversa + +: ovipositor 2.09× as long as mid tibia (2.26×), third valvula 0.46× mid tibia length (0.52×), and mid lobe of mesoscutum with 8 setae (6). + + + + \ No newline at end of file diff --git a/data/38/0E/27/380E272D53D81D657E0F13D0B91D23D4.xml b/data/38/0E/27/380E272D53D81D657E0F13D0B91D23D4.xml new file mode 100644 index 00000000000..79ee15b1922 --- /dev/null +++ b/data/38/0E/27/380E272D53D81D657E0F13D0B91D23D4.xml @@ -0,0 +1,190 @@ + + + +Order Chiroptera - Family Vespertilionidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +451 +529 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Myotis volans +H. Allen 1866 + + + + + + + +Myotis volans +H. Allen 1866 + +, + +Proc. Acad. Nat. Sci. +Philadelphia +, 18: 282 + + +. + + + + +Type Locality: + +Mexico +, +Baja California +, Cabo San Lucas. + + + + + +Vernacular Names: +Long-legged Myotis +. + + + + +Subspecies: +: + + +Subspecies + +Myotis volans +subsp. +volans +H. Allen 1866 + + + +Subspecies + +Myotis volans +subsp. +amotus +Miller 1914 + + + +Subspecies + +Myotis volans +subsp. +interior +Miller 1914 + + + +Subspecies + +Myotis volans +subsp. +longicrus +True 1886 + + + + + +Distribution: +Jalisco +to +Veracruz +( +Mexico +); +Alaska +Panhandle ( +USA +) to +Baja California +( +Mexico +), east to N +Nuevo León +( +Mexico +), +South Dakota +( +USA +), and C +Alberta +( +Canada +). + + + + +Conservation: +IUCN +2003 and +IUCN +/ +SSC +Action Plan (2001) – Lower Risk (lc). + + + + +Discussion: +Revised by +Miller and Allen (1928) +. See +Warner and Czaplewski (1984) +. Apparently closely related to + +lucifugus + +and + +thysanodes + +; see +Ruedi and Mayer (2001) +. + + + + \ No newline at end of file diff --git a/data/38/0E/87/380E87A6F161FF9F3181FE12FA645923.xml b/data/38/0E/87/380E87A6F161FF9F3181FE12FA645923.xml new file mode 100644 index 00000000000..a7b5a341b77 --- /dev/null +++ b/data/38/0E/87/380E87A6F161FF9F3181FE12FA645923.xml @@ -0,0 +1,379 @@ + + + +Review of the Kimminsula-complex (Ephemeroptera, Leptophlebiidae) + + + +Author + +Kluge, Nikita J. +0000-0001-9741-7790 +n.kluge@spbu.ru. + +text + + +Zootaxa + + +2022 + +2022-11-22 + + +5212 + + +1 + + +1 +140 + + + + +http://dx.doi.org/10.11646/zootaxa.5212.1.1 + +journal article +202082 +10.11646/zootaxa.5212.1.1 +8d28a58f-680c-4495-b569-1b97c435a9d3 +1175-5326 +7345276 +485EA061-41EA-4E0C-894D-593B84DB41D8 + + + + + +Key to larvae of the + +Kimminsula + +-complex + + + + + + + + +1(10) Each of two lamellae of each tergalius with numerous slender processes ( +Figs 43–48 +, +85–90 +, +130–136 +, +148–150 +, +641–663 +)..................................................................................................... 2 + + + + + + +2(3) Only posterior margin of each lamella with processes ( +Figs 641–663 +)............... + + +Hubbardula heterolepida + +gen. sp. n. + + + + + + + +3(2) Both margins of each lamella with processes ( +Figs 43–48 +, +85–90 +, +130–137 +, +148–150 +)............................... 4 + + + + + + +4(7) Labrum as wide as clypeus ( +Figs 7 +, +72 +). Patella-tibial suture absent on foreleg, present on middle and hind legs, crosses inner side of tibia ( +Figs 30–34 +). 6 pairs of tergalii (tergalii VII lost) ( +Figs 43–48 +, +85–90 +). ( + + +Ghatula + +gen. n. + +).................. 5 + + + + + + +5(6) Abdominal terga VIII and IX each with pair of dark brown maculae ( +Figs 68–69 +). On forefemur, inner-anterior flange larger than inner-posterior flange ( +Fig. 78 +)............................................... + + +Ghatula quadrimaculata + +sp. n. + + + + + + + +6(5) Abdominal terga without contrasting maculae ( +Fig. 15 +). On forefemur, inner-anterior flange smaller than inner-posterior flange ( +Fig. 27 +)......................................................................... + + +Ghatula rufa + +gen. sp. n. + + + + + + + +7(4) Labrum normally much wider than clypeus ( +Fig. 96 +) (not much wider in selected individuals). Patella-tibial suture equally developed on all legs, not crossing inner side of tibia ( +Figs 124–128 +). 7 pairs of tergalii ( +Figs 130–136 +) ( + +Petersula + +) (larva of + +P. nathani + +unknown)..................................................................................... 8 + + + + + + +8(9) Posterolateral spines of uromere VIII longer than spines of uromere IX ( +Fig. 94 +)........... + + +Petersula heptagenoides + +sp. n. + + + + + + + +9(8) Posterolateral spines of uromere VIII shorter than spines of uromere IX ( +Fig. 196 +)................ + +Petersula courtallensis + + + + + + + +10(1) Each of two lamellae of each tergalius with one slender process at apex, without additional slender processes ( +Figs 262–268 +, +348–361 +, +399–405 +, +507–527 +, +587–600 +)................................................................... 11 + + + + + + +11(12) Each of two lamellae of each tergalius without projections by sides of apical process ( +Figs 262–268 +)... + +Ceylonula femoralis + + + + + + + +12(11) Each of two lamellae of each tergalius wit two projections by sides of apical process, so that apical process is inserted in incision between them ( +Figs 348–361 +, +399–405 +, +507–527 +, +587–600 +) ( + +Kimminsula + +) form intermediate between + +K. taprobanes + +and + +K. fasciata + +is not included in this key).................................................................... 13 + + + + + + +13(14) Labrum relatively wide and short ( +Figs 552–553 +). Stout setae on femora small and blunt ( +Figs 569–673 +). Inner side of foretibia without stout pointed setae (with only a few such setae at apex) ( +Figs 574–575 +)............... + + +Kimminsula latifolia + +sp. n. + + + + + + + +14(13) Labrum narrower and shorter ( +Figs 322 +, +389 +, +444 +, +478 +). Stout setae on femora longer ( +Fig. 336–338 +, +395 +, +494–495 +). Inner side of foretibia with stout pointed setae ( +Figs 339 +, +499 +)......................................................... 15 + + + + + + +15(16) Outer margins of femora not bordered with brown ( +Figs 392–394 +). Each abdominal tergum II–VIII with unpaired median blank bordered with dark area in front but not behind ( +Fig. 390 +) (this blank can be bordered from behind with dark area of hypodermal coloration)........................................................................ + +Kimminsula taprobanes + + + + + + + +16(15) At least outer margin of fore- and middle femora bordered with dark brown (both cuticular and hypodermal colorations) ( +Figs 336–338 +, +367 +, +496–498 +). If contrasting pigmented areas and blanks expressed on cuticle of abdominal terga, tergum has paired or unpaired median blank bordered from behind ( +Figs 329–331 +, +480 +)........................................... 17 + + + + + + +17(18) Tibia with hypodermal coloration not darker than hypodermal coloration of femur ( +Fig. 367 +). Cuticle of clypeus usually with pair of contrasting blanks ( +Fig. 322 +)...................................................... + +Kimminsula fasciata + + + + + + + +18(17) Tibiae with hypoderm entirely colored with brown or black, darker than hypodermal coloration of femur ( +Figs 573–538 +). Cuticle of clypeus without contrasting blanks ( +Fig. 478 +)....................................... + + +Kimminsula podi + +sp. n. + + + + + + + + \ No newline at end of file diff --git a/data/38/0E/87/380E87A6F164FF9F3181FBC6FA645E9E.xml b/data/38/0E/87/380E87A6F164FF9F3181FBC6FA645E9E.xml new file mode 100644 index 00000000000..846284dfdff --- /dev/null +++ b/data/38/0E/87/380E87A6F164FF9F3181FBC6FA645E9E.xml @@ -0,0 +1,1027 @@ + + + +Review of the Kimminsula-complex (Ephemeroptera, Leptophlebiidae) + + + +Author + +Kluge, Nikita J. +0000-0001-9741-7790 +n.kluge@spbu.ru. + +text + + +Zootaxa + + +2022 + +2022-11-22 + + +5212 + + +1 + + +1 +140 + + + + +http://dx.doi.org/10.11646/zootaxa.5212.1.1 + +journal article +202082 +10.11646/zootaxa.5212.1.1 +8d28a58f-680c-4495-b569-1b97c435a9d3 +1175-5326 +7345276 +485EA061-41EA-4E0C-894D-593B84DB41D8 + + + + + + +Key to imagines of Asian +Leptophlebiidae +with both claws of each leg pointed + + + + + + + + + +1(2) Hind wings absent............................................................................ + +Nathanella + + + + + + + +2(1) Hind wings present ( + + +Kimminsula + +-complex + +)................................................................ 3 + + + + + + +3(4) Paracercus vestigial, about as long as 10th abdominal segment ( +Fig. 271 +)......................... + +Ceylonula femoralis + + + + + + +4(3) Paracercus as long as cerci. + + + + + +5(8) Vein MP of hind wing not furcated ( +Fig. 52 +). Tibiae of middle and hind legs with groove crossing inner margin and corresponding to patella-tibial suture ( +Figs 54–55 +) ( + + +Ghatula + +gen. n. + +)..................................................... 6 + + + + + + +6(7) Abdominal terga VIII and IX each with pair of dark brown maculae (as in +Fig. 69 +) (presumably, based on larval hypodermal coloration)................................................................... + + +Ghatula quadrimaculata + +sp. n. + + + + + + + +7(6) Abdominal terga VIII and IX without such maculae ( +Figs 57–58 +)................................ + + +Ghatula rufa + +sp. n. + + + + + + + +8(5) Vein MP of hind wing furcated: either with intercalary forming triad ( +Fig. 153 +, +157 +), or without intercalary ( +Fig. 217 +), or with both branches fused distally ( +Fig. 158 +). All tibiae (including those of middle and hind legs) without groove crossing inner margin ( +Figs 159–164 +, +213–214 +, +461–462 +, +680–681 +)............................................................ 9 + + + + + + +9(12) Hind wing with anterior-proximal margin bordered with brown ( +Figs 157–158 +, +671 +)............................... 10 + + + + + + +10(11) Hind wing with posterior-distal margin bordered with brown ( +Figs 157–159 +). + +: eyes meet on meson ( +Fig. 168 +); penis with pair of apical spines directed ventrally ( +Figs 172–173, 179 +, +183 +)............................ + + +Petersula heptagenoides + +sp. n. + + + + + + + +11(10) Hind wing with posterior-distal margin not colored ( +Fig. 671 +). + +: eyes widely separated ( +Fig. 674 +); penis without spines directed ventrally ( +Figs 688, 690 +, +697 +)......................................... + + +Hubbardula heterolepida + +gen. sp. n. + + + + + + + +12(9) Hind wing with brown coloration at base only ( +Figs 217 +, +365 +, +412 +, +454 +, +540 +)..................................... 13 + + + + + + +13(16) + +: dorsal eyes meet on meson (as in +Fig. 168 +); ventral spines on apices of penis grooved (as in +Figs 172–173, 179 +; Sivaramakrishnan 1984: fig. 6, 9) ( + +Petersula + +)...................................................................... 14 + + + + + + +14(15) + +imago: abdominal terga III–V without paired lines (Sivaramakrishnan 1984: figs 10, 12); terga I–IX light, tergum X dark................................................................................... + +Petersula courtallensis + + + + + + + +15(14) + +imago: abdominal terga III–V with submedian pair of longitudinal lines (Sivaramakrishnan 1984: fig. 11); terga I–VII light, terga VIII–X dark....................................................................... + +Petersula nathani + + + + + + + +16(13) + +: dorsal eyes widely separated ( +Figs 369 +, +531 +); ventral spines on apices of penis cone-shaped, without groves ( +Figs 374–375 +, +377 +, 380,417, 418, 421, 469–470, 534, 545) ( + +Kimminsula + +)................................................... 17 + + + + + + +17(18) Each abdominal tergum V–VIII or V–IX with unpaired triangular dark spot adjacent to anterior margin of tergum (as in +Fig. 580 +) (presumably, based on larval hypodermal coloration)................................ + + +Kimminsula latifolia + +sp. n. + + + + + + +TABLE 1. +Generic characters. Columns: I: numbers in «Common characters of the +Kimmiunsula +-complex»; II: numbers in generic diagnoses; III: characters. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
IIIIII + +Ghatula + + +gen.n. + + + +Petersula + + + +Ceylonula + + +gen.n. + + + +Kimminsula + + + +Hubbardula + + +gen.n. + +
+Larval characters: +
3Labrum +non-widened +widenedwidenedwidenedwidened
Figs 7Fig. 96Fig. 221Fig. 478Fig. 616
3 +1 +Labrum: median incision +cleft-like + +cleft-like +5 denticles5 denticles5 denticles
Figs 17, 73Fig. 103Figs 232–233Fig. 487Fig. 619
3 +2 +Labrum: paired depressorsabsent +present +absentabsentabsent
Figs 101, 106–107
4 +3 +Mandible: middle tuftpresent +absent +presentpresentpresent
Figs 75–76Figs 145–146Fig. 229Figs 563Figs 620
4 +4 +Mandible: proximal branch of prosthecapresent +absent +presentpresentpresent
Fig. 75–76Figs 108–110Fig. 230–231Figs 562–563Figs 620–621
5 +5 +Maxilla: lateral portion of subapical ventral setal rowshortshort +long + +long + +long +
Fig. 20Fig. 113Fig. 237Figs. 332–333Fig. 623
6 +6 +2nd segment of maxillary palp: setae on inner marginrow +tuft +rowrowrow
Fig. 19Fig. 111Fig. 236Fig. 493Fig. 623
11 +7 +a +Patella-tibial suture on foreleg:absent +incomplete +absentabsentabsent
Fig. 30Fig. 124Fig. 251Fig. 339Fig. 632
11 +7 +b +Patella-tibial suture on middle leg:present +incomplete +presentpresentpresent
Fig. 32Fig. 127Fig. 257Figs 341–343Figs 634–636
11 +7 +c +Patella-tibial suture on hind leg:present +incomplete +present +incomplete +present
Figs 33–34Fig. 128Fig. 258Figs 344–345Figs 637–638
11 +8 +Outer-anterior row of hairs on all tibiaeabsent +present +absent +present + +present +
Figs 30–35Fig. 124Fig. 251–260Fig. 501, 576Fig. 635
15 +9 +Tergalii +bipectinate + +bipectinate +simple +incised + +pectinate +
Figs 43–48,Figs 130–136Figs 261–268Figs 348–361,Figs 641–663
85–90399–404, 507–527,
587–600
15 +10 +Tergalius VII +absent +presentpresentpresentpresent
Spines on larval protopenis?present +absent + +absent +absent
Figs 175–177Fig. 503Figs 425–426Fig. 696
+
+ +......continued on the next page + +TABLE 1. (Continued) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
IIIIII + +Ghatula + + +gen.n. + + + +Petersula + + + +Ceylonula + + +gen.n. + + + +Kimminsula + + + +Hubbardula + + +gen.n. + +
+Imaginal characters: +
16 +11 +Hind wing: fork MP +absent +presentpresentpresentpresent
Fig. 52Figs 157–158Fig. 316Fig. 412Fig. 671
+7 +d +Patella-tibial suture on middle and hind legs:present +absent +present +absent + +absent +
Figs 54–55Fig. 163–164Figs 274–276,Figs 461–462Figs 680–681
278–288
+12 +Paracercuslonglong +vestigial +longlong
Fig. 57Fig. 165Fig. 270–271Fig. 458Fig. 675
18 +13 +Medioventral spines on penes:? +grooved +laterally + +grooved +medially + +con-shaped + +absent +
Figs 172–173Figs 300–301Fig. 380Fig. 697
19 +14 +a +Styliger?short +long medially +short +long laterally +
Fig. 184Fig. 296Fig. 376Fig. 698
19 +14 +b +Gonostylus: 3rd segment?short +elongate +short +fused +
Fig. 183Fig. 295Fig. 376Fig. 698
19 +14 +c +Gonostylus: 4th segment?short +elongate +shortshort
Fig. 183Fig. 295Fig. 376Fig. 698
+15 +Setae-bearing convexity behind female gonoporeabsentabsent +present + +present + +present +
Figs 169Figs 308–310Fig. 428Figs 702–706
+
+ + + +18(17) Abdominal terga either without smaller dark spots ( +Figs 369–370, 373 +, +463 +, +532 +), or with large spot adjacent to posterior margin of tergum ( +Figs 414, 416 +)........................................................................... 19 + + + + + + +19(20) + +: penis with unpaired projection between pair of lobes ( +Figs 534 +, +545 +); tibiae black-brow, contrastingly darker than femora ( +Figs 535–536 +); abdominal coloration as in +Fig. 532 +........................................ + + +Kimminsula podi + +sp. n. + + + + + + + +20(19) + +: penis lobes contiguous basally, without projection between them ( +Figs 374–375 +, +377, 380 +); tibiae brown or ocher, not darker than femora ( +Figs 370 +, +414 +); abdominal coloration different ( +Figs 369–370, 373 +, +414, 416 +, +463 +)...................... 21 + + + + + + +21(22) Abdominal terga mostly brown, with antero-lateral areas lighter ocher ( +Figs 413–416 +)............ + +Kimminsula taprobanes + + + + + + + +22(21) Abdominal terga mostly light ocher, with brown markings ( +Figs 369–370, 373 +, +463 +).............................................................. + +Kimminsula fasciata + +(and the form intermediate between + +K. taprobanes + +and + +K. fasciata + +) + + + +
+
+
+
\ No newline at end of file diff --git a/data/38/0E/87/380E87A6F168FF9A3181FE23FDD45CE4.xml b/data/38/0E/87/380E87A6F168FF9A3181FE23FDD45CE4.xml new file mode 100644 index 00000000000..205883b798f --- /dev/null +++ b/data/38/0E/87/380E87A6F168FF9A3181FE23FDD45CE4.xml @@ -0,0 +1,1280 @@ + + + +Review of the Kimminsula-complex (Ephemeroptera, Leptophlebiidae) + + + +Author + +Kluge, Nikita J. +0000-0001-9741-7790 +n.kluge@spbu.ru. + +text + + +Zootaxa + + +2022 + +2022-11-22 + + +5212 + + +1 + + +1 +140 + + + + +http://dx.doi.org/10.11646/zootaxa.5212.1.1 + +journal article +202082 +10.11646/zootaxa.5212.1.1 +8d28a58f-680c-4495-b569-1b97c435a9d3 +1175-5326 +7345276 +485EA061-41EA-4E0C-894D-593B84DB41D8 + + + + + + + +Kimminsula + +-complex + + + + + + +( +Figs 3 +, +7–710 +) + + + + +The + +Kimminsula + +-complex belongs to subsequently subordinated taxa: +Leptophlebiidae +>Atalophleboadentata +Kluge 2009 +> Atalophlebopectinata +Kluge 2009 +> Atalophleboculata +Kluge 2009 +> Atalophlebomaxillata +Kluge 2009 +> Atalophlebolinguata +Kluge 2009 +. General system of the taxon Atalophlebolinguata remains poorly elaborated. + + + + +The + +Kimminsula + +-complex is distributed only in the Indian Peninsula and the Island of +Sri Lanka +and includes + +Kimminsula +Peters & Edmunds 1970 + +(with 3–5 species), + +Petersula +Sivaramakrishnan 1984 + +(with 2–3 species), + +Ghatula + + +gen. n. + +(with 2 species), + +Ceylonula + + +gen. n. + +(with 1 species) and + +Hubbardula + + +gen. n. + +(with 1 species). Larvae of all these species are similar in general appearance [see (1) below]; characters separating larvae of the + +Kimminsula + +-complex from other taxa with a similar larval appearance are the presence of fronto-clypeal incisions [see (2) below] and a characteristic shape and setation of femora [see (10) below]. Imagines of the + +Kimminsula + +-complex differ from other Oriental Leptoplebiidae by well developed hind wings of plesiomorphic shape and venation [see (16) below] and by the claw structure [see (17) below]. + + + + + +Common characters of the + +Kimminsula + +-complex + + + +(1) General appearance. +Larva has flattened body, widened head and enlarged legs with broad femora and claws bent perpendicular to the leg flatness ( +Figs 202 +, +440–443 +). Superficially, they resemble larvae of +Heptageniidae +, but in contrast to them have no frontal shield; instead, the wide dorsal head surface contains surfaces of closely pressed together clypeus, labrum and mandibles ( +Fig. 235 +) (the same in other Atalophlebomaxillata). Initially such larval structure is an adaptation for inhabiting stone surfaces in rapidly running water ( +Fig. 219 +), but larvae of + +Ceylonula femoralis + +inhabit soft substrates in stagnant water ( +Fig. 220 +). + + +(2) Fronto-clypeal incisions. +Lateral margins of the clypeus are separated from lateral margins of the frons by a pair of sharp incisions leading into the anterior tentorial pits; within these incisions, the margins of the frons overlap the margins of the clypeus dorsally ( +Figs 3 +, +14 +, +68 +, +105 +, +235 +, +335 +, +389 +, +444 +, +485 +, +552–553 +, +616 +). This differs from many other Atalophlebolinguata, where the frons and the clypeus have an integral dorsal surface, being separated only by a pair of smooth concavities of the lateral margins ( +Figs 5–6 +) (see below, discussion of systematic position of the + +Kimminsula + +-complex). + + +(3) Labrum. +As in most other Atalophlebopectinata, the dorsal surface of the labrum bears the +posterior transverse setal row +and the +anterior transverse setal row +; in the + +Kimminsula + +-complex both rows stretch nearly across the labrum width; each row is dense, either regular, i.e. with one seta per section ( +Figs 16 +, +73 +, +232 +: anter.r, 488, 619), or has the form of a strip with a few setae per section ( +Figs 102 +, +232 +: poster.r, 617). In all species of + +Kimminsula + +-complex, the anterior margin of labrum is hooded, i.e. the initial anterior margin is bent ventrally, so that in dorsal view the posterior transverse setal row appears to be located on the visible anterior margin or close to it, while the anterior transverse setal row is often hidden ventrally ( +Fig. 101 +). Setae of the true ventral side of labrum are situated irregularly (i.e. not forming rows), and form a distinctly outlined transverse +ventro-anterior strip +close to the anterior margin ( +Figs 101, 103 +). In all species except + +Ghatula rufa + +gen. sp. n. +, labrum is wider than clypeus. Shape of the median incision is variable: either shallow with more or less developed denticles on the initial anterior margin (in the Ceylonese taxa + +Ceylonula + + +gen. n. + +, + +Kimminsula + +and + +Hubbardula + + +gen. n. + +, +Figs 233 +, +487 +, +619 +), or cleft-like and lacking denticles (in the Indian taxa + +Ghatula + + +gen. n. + +and + +Petersula + +, +Figs 17 +, +103 +). + +Petersula + +differs from other taxa by peculiar labral depressors [see below, + +Petersula + +(2)] + + + +FIGURES 1–6. +Junction of frons and clypeus in larvae of +Leptophlebiidae +(left margin, dorsal view). 1, + +Leptophlebia vesperina +(Linnaeus 1758) + +; 2. + +Terpides echinovaris +Kluge 2015 + +; 3, + +Ceylonula femoralis +( +Hagen 1858 +) + +; 4, + +Thraulus bellus +Eaton 1881 + +; 5, + +Choroterpes picteti +( +Eaton 1871 +) + +; 6, + +Meridialaris chiloeensis +(Demoulin 1955) + +. Abbreviations: +cly +, clypeus; +c.md +, anterior mandibular condyle; +fr +, frons; +lbr +, labrum. + + + +(4) Mandibles. +As in majority of Atalophlebolinguata, mandibles are articulated at ventral side of the head capsule some distance from its lateral margins ( +Fig. 235 +); mandibles are flattened, with outer margins convex and projected laterally. The outer margin of mandible bears the +distal tuft +of setae, which occupies an area adjacent to the base of the incisor, and the +middle tuft +of setae which is more compact and located more laterally ( +Figs 22–23 +, +75–76 +, +229 +, +563 +, +620 +). Among members of the + +Kimminsula + +-complex, the middle tuft is absent only in + +Petersula + +( +Figs 145–146 +). The same in some other leptophlebiid taxa ( +Kluge 2020 +). + + +(5) Maxillae. +Maxilla is wide. The +subapical ventral row of comb-like setae +(peculiar for +Leptophlebiidae +) has more or less expressed curvature, which divides it into two portions: a +lateral +portion consisting of setae with smaller sockets, and a +median +portions consisting of setae with larger sockets (length of all setae is equal). In the Ceylonese taxa, i.e. + +Ceylonula + + +gen. n. + +, + +Kimminsula + +and + +Hubbardula + + +gen. n. + +, the lateral portion is very long and the median portion is short, consisting of 5–10 setae ( +Figs 332–334 +). In the Indian taxa, i.e. + +Ghatula + + +gen. n. + +and + +Petersula + +, the whole subapical ventral setal row is shorter, and its both portions are subequal in length ( +Figs 112–113 +) (the same in many other leptophlebiid taxa). + + +(6) Maxillary palps. +Maxillary palp bears long setae on outer sides of the 2nd and 3rd segments, dense setae on ventral side and on apex of the 3rd segment. The inner side of the 3rd segment bears a regular row of setae, whose size and number vary individually and do not provide taxonomic characters within the +Kimminsulacomplex +. The inner side of the 2nd segment bears longer setae which are either concentrated at its apex (in both species of + +Petersula + +, +Fig. 111 +) or form a more or less long longitudinal row (in other species, +Figs 19 +, +236 +, +334 +, +493 +, +566 +, +623 +). + + +(7) Labium. +Shape and setation of labium is uniform in all representatives ( +Figs 26 +, +77 +, +116–118 +, +241 +, +492 +, +567 +, +624–625 +). Submentum is bare without prominent setae: either without visible setae at all ( +Figs 116 +, +567 +, +625 +), or with very small occasional setae. The glossae are not large, not projected from paraglossae neither ventrally, nor dorsally; long setae of their ventral side are situated densely and irregularly ( +Fig. 625 +); long setae on the dorsal side of glossa form irregular row or strip of a horseshoe shape ( +Fig. 242 +, +624 +) [as in +Thaulodes +(Kuge 2020: fig. 20)]. + + +(8) Labial palps. +The last (3rd) segment of labial palp is shorter and narrower than others and apically blunt. A small, regular row of stout claw-like setae crosses apex of this segment. In + +Petersula + +, these claw-like setae are relatively long ( +Fig. 117 +); in other taxa they are very short, with length about twice exceeding width at base ( +Figs 25 +, +240 +, +492 +, +567 +, +626 +). The same condition occurs in most other Atalophleboculata (see discussion about systematic position below). + + +(9) Larval thorax. +The pronotum is nearly rectangular, with rounded antero-lateral angles and a free anterior margin (i.e. transverse margin between antero-lateral angles and the neck membrane); a transverse ridge runs parallel to the free anterior margin; humeral setae are located between the free anterior margin and the ridge, being absent in other places ( +Figs 9 +, +91 +, +95 +, +228 +, +324 +, +391 +, +481 +, +556 +, +610 +) (the same in many other Atalophlebolinguata). + + +(10) Larval femora. +Femora are widened, so the groove on inner side (into which the tibia can be partly inserted) is bordered with prominent flanges (called here the +inner-anterior flange +and the +inner-posterior flange +); at least on the middle femur, the inner-anterior flange is expanded in its distal part, so the femur appears widest in distal part ( +Fig. 28 +); the forefemur has similar shape in all species except + +Ghatula rufa + +gen +sp. n. +, in which the inner-anterior flange of forefemur is reduced, being narrower than the inner-posterior flange ( +Fig. 27 +); the hind femur retains the usual elongate-ellipsoid shape, being widest in the middle ( +Fig. 29 +). + + +The forefemur is not widened proximally (in contrast to many other +Leptophlebiidae +), but the cuticle of its anterior surface bears the +proximal blank +peculiar for mayfly larvae whose forefemur is proximally wider ( +Kluge 2020 +: p. 15). The proximal blank of foreleg differs from blanks occurring on the middle and hind legs ( +Fig 27 +, +119 +, +243 +, +336 +, +392 +, +449 +, +496 +, +571 +, +626 +). + + +The anterior surface of each femur bears more or less numerous, irregularly situated, +stout setae +, which can be either blunt ( +Fig. 494 +), or pointed ( +Fig. 495 +), or variable. On the inner side of the femur the stout setae form a more or less regular row running by margin of the inner-anterior flange. On middle and hind femora (but never on forefemur) the stout setae form a regular, arched, +transverse row +situated near the femur base ( +Figs 28–29 +, +79–80 +, +120–121 +, +245 +, +337–338 +, +497–498 +, +572–573 +, +627 +). On outer side of each femur the stout setae are enlarged and form two more or less regular rows (which can be called the +outer-anterior row +and the +outer-posterior row +), between which the +outer strip of thin hairs +is located; hairs of this strip are situated densely and irregularly ( +Fig. 629 +). Hairs of the outer strip are generally longer and/or denser on the fore- and the middle femora, than on the hind femur ( +Figs 27–29 +, +78–80 +, +119–121 +, +336–338 +, +392–394 +, +449–451 +, +496– 498 +, +571–573 +, +612–614 +); in + +Ceylonula + + +gen. n. + +they are completely absent on the hind femur ( +Fig. 245 +). The posterior side of the hind femur bears +curved setae +—these are small, pointed, usually pectinate setae, curved toward the inner margin of the femur and forming an irregular strip along inner margin of the femur ( +Figs 36 +, +123 +, +247 +). + + +The curved setae are probably initial for +Leptophlebiidae +; other features of femur setation, especially the transverse proximal rows on middle and hind femora, distinguish the + +Kimminsula + +-complex from many other +Leptophlebiidae +(see below, discussion about systematic position of the + +Kimminsula + +-complex). + + +(11) Larval tibiae. +Patella-tibial suture, which initially for mayflies is absent on the forelegs and present on the middle and the hind legs ( +Kluge 2004 +), retains this condition in +Ghatula + +gen. n. + +, + +Ceylonula + + +gen. n. + +and + +Hubbardula + +gen.n. +; it is differently modified in + +Petersula + +and in + +Kimminsula + +[see below, + +Petersula + +(7) and + +Kimminsula + +(7)]. + + +As in most other +Leptophlebiidae +, tibiae of three leg pairs are differentiated: the pointed pectinate setae of inner side are preferably developed on the foreleg, and the stout setae of outer side are preferably developed on the hind leg. + + +The foretibia bears stout pointed setae, which are often bipectinate; these setae occupy a longer or shorter part of the inner side of the foretibia, being always present at least near the apex of the tibia ( +Figs 124–126 +, +253–254 +, +339–340 +, +574–575 +, +632–633 +); on the middle tibia such setae are present only in + +Ceylonula + + +gen. n. + +( +Figs 255–256 +); on the hind tibia such setae are absent in all representatives of the + +Kimminsula + +-complex. + + +The hind tibia differs from other tibiae by the presence of stout setae located on all sides, forming two longitudinal rows on outer side of the tibia—the outer-posterior and the outer-anterior ones ( +Figs 258 +, +504–505 +, +639 +) and forming a transverse row on posterior side at the tibia apex ( +Figs 35 +, +259 +). + + +As in many other +Leptophlebiidae +, the outer side of each tibia bears a longitudinal row of hairs (long and slender setae). In + +Ghatula + + +gen. n. + +and + +Ceylonula + + +gen. n. + +this row of hairs is single, but + +Petersula + +, + +Kimminsula + +and + +Hubbardula + + +gen. n. + +have a second row located more anteriorly. Each of these rows is either regular, i.e. with one seta per section ( +Figs 124–125 +, +342 +, +501 +), or has a form of strip with a few setae per section ( +Figs 576 +, +639 +). On the hind tibia, which has two rows of stout setae on the outer side, the initial outer row of hairs is located between them, and the additional anterior row of hairs is located anteriad of the outer-anterior row of stout setae ( +Fig. 639 +). + + +(12) Larval tarsus. +The tarsus of each leg pair bears hairs on the outer side similar to hairs on the tibia; these hairs are longer and denser on the hind leg. Stout setae on inner sides of tarsi are differentiated as follows: on the fore- and middle legs they are small and few, can be absent; on the hind leg stout setae always form a longitudinal row at least on the distal part of the tarsus; in proximal part of the row setae are sparse and small, but they become denser, larger and hooked toward apex of the tarsus ( +Fig. 35 +). Sometimes inner side of the foretarsus bears several stout, pointed, pectinate setae of the same structure as the setae on inner side of the tibia of the same leg; such setae occur in + +Ceylonula femoralis + +( +Figs 251, 253 +) and some others. + + +(13) Larval claw. +Claw is bent perpendicular to the leg flatness and distinctly divided into the small +articulatory portion +and the large +rigid portion +( +Figs 129 +, +506 +) ( +Kluge 2020 +). + + +(14) Larval abdomen. +The surface of terga and sterna is always smooth, without prominent relief or significant setae. Posterior margin of each abdominal tergum bears a row of sharply pointed denticles greatly varying in size; medium size of denticles is either subequal on all terga I–X ( +Figs 38–41 +), or significantly differs on different terga. Posterior margin of the 10th tergum always has shallow median concavity ( +Figs 41 +, +398 +, +586 +, +631 +). Posterior margins of all sterna I–IX are always smooth, without denticles ( +Fig. 94 +). + + +Caudalii are about 2–3 times longer than the body; all 3 caudalii (the cerci and the paracercus) are equally developed both in + +Ceylonula femoralis + +(whose paracercus is vestigial in the winged stages, +Figs 269–271 +) and in other species (where the paracercus is equal to the cerci in all stages); posterior margin of each segment of cercus and paracercus bears whorls of pointed denticles and setae in all species ( +Figs 41–42 +). + + +(15) Tergalii. +Tergalii always retain 2 lamellae (initial for +Leptophlebiidae +); tergalii of all pairs have similar structure, with both lamellae similar. Tergalii make rhythmic undulate movements with the wave going from front to back; either all pairs of tergalii participate equally in respiration ( +Figs 440–442 +) or tergalii I do not participate in respiratory movement ( +Fig. 202 +). In other respects, structure of tergalii significantly differs in different taxa [see below, + +Ghatula + +(9), + +Petersula + +(9), + +Ceylonula + +(9), + +Kimminsula + +(9) and + +Hubbardula + +(9)]. All 7 pairs of tergalii are retained in + +Petersula + +, + +Ceylonula + + +gen. n. + +, + +Kimminsula + +and + +Hubbardula + + +gen. n. + +, while + +Ghatula + + +gen. n. + +has no tergalii of 7th pair, thus retains only 6 pairs of tergalii. + + +(16) Forewings. +Furcation of MA is symmetrical or slightly asymmetrical. Furcation of MP is more proximal than furcation of RS and is sharply asymmetrical: vein MP +2 +is attached at base to veins MP +1 +and CuA either by equally oblique crossveins ( +Fig. 411 +), or the crossvein connecting MP +2 +with MP +1 +is more oblique and may be interpreted as asymmetric arising of MP +2 +from MP +1 +( +Figs 51 +, +68 +, +151 +, +156 +, +279 +, +453 +, +539 +, +670 +); this difference may be individual ( +Figs 216, 218 +). Cubital field has +2 intercalaries +between Cu +1 +and Cu +2 +; in + +Kimminsula latifolia + + +sp. n. + +a third, additional intercalary is present between them ( +Fig. 581 +). Crossveins are numerous; some crossveins reach posterior margin of the wing between ends of the longitudinal and the intercalary veins. Crossveins in the area of pterostigma are numerous, complete and non-anastomosed; in + +Ceylonula femoralis + +the costal field is wider than the subcostal field, and the pterostigmatic crossveins are nearly perpendicular to Sc ( +Fig. 279 +); in other taxa the costal field is not wider than the subcostal field, and the pterostigmatic crossveins vary from sharply oblique ( +Fig. 414 +) to perpendicular to Sc ( +Figs 670 +). + + +(17) Hind wings. +Forewing has well expressed tornus, and the hind wing is relatively large, about as long as the basi-tornal margin of the forewing. Costal projection of the hind wing is blunt and slightly projected; Sc is continued far distad of the costal projection ( +Figs 52 +, +153 +, +157–158 +, +217 +, +278 +, +365 +, +412 +, +454 +, +540 +, +671 +). The vein MA is non-bifurcate as in all other Furcatergaliae (see +Kluge 2004 +); other veins are either fully developed ( +Figs 157–158 +), or MP is non-bifurcate (in + +Ghatula + + +gen. n. + +, +Fig. 52 +). + + +(18) Claws of winged stages. +On each leg of imago and subimago, both claws are pointed and hooked ( +Figs 289 +, +676 +) (see below, discussion about systematic position of the + +Kimminsula + +-complex). + + +(19) Penis. +The pair of penis lobes are movably connected at base, so that are able to move apart and be brought together under action of the sterno-penial muscles. In + +Petersula + +the penial lobes are separated nearly to the base ( +Figs 179 +, +183 +), while in + +Ceylonula + + +gen. n. + +, + +Kimminsula + +and + +Hubbardula + + +gen. n. + +, the median sides of penis lobes are connected one with another at significant distance ( +Figs 297 +, +301 +, +375 +, +377 +, +418 +, +421 +, +469–470 +, +534 +, +545 +, +690 +, +697 +); in the last case their mobility is ensured by the fact that the cuticle of these median areas is delicate, soft and elastic. + + +In + +Petersula + +, + +Kimminsula + +and + +Ceylonula + + +gen. n. + +, apex of each paired penis lobe bears a pointed process directed medio-ventrally; such processes are not present in in + +Hubbardula + + +gen. n. + +( +Figs 690 +, +697 +); genitalia of + +Ghatula + + +gen. n. + +are unknown. In taxa with the medio-ventral processes, these processes arise from the penis apices and look similarly, but their structure is significantly different: in + +Kimminsula + +they are conic, i.e. round in cross section ( +Figs 374–375 +, +377, 380 +, +417–418 +, +421 +, +469–470 +, +545 +), in + +Ceylonula + + +gen. n. + +they are grooved with concavities facing medio-dorsally ( +Figs 300–301 +), and in + +Petersula + +they are grooved with concavities faced latero-ventrally ( +Figs 172–173, 179 +). + + +In + +Petersula + +, the pointed projections are already present on larval protopenis, where they have the same position as in imago ( +Figs 175–177 +, +209 +). In + +Ceylonula + + +gen. n. + +and + +Kimminsula + +, larval protopenis has no any precursors of these projections ( +Figs 304–305 +, +379 +, +425–426 +, +549 +, +602 +). + + +In all cases (in + +Petersula + +, + +Kimminsula + +, and + +Ceylonula + + +gen. n. + +) the medio-ventral pointed processes arise from the ventral sides of penis lobes, significantly distad to the gonopores, while the gonopores are opened on the dorsal sides of the penis lobes. The medio-ventral pointed processes have no connection with the gonoducts: in + +Petersula + +and + +Ceylonula + + +gen. n. + +their grooves do not touch the gonopores ( +Figs 172 +, +300 +), and in + +Kimminsula + +they have no any grooves or canals at all. The pair of gonoducts passing inside the penis lobes, have no musculated sperm pumps, in contrast to + +Thraulodes + +( +Kluge 2020 +: figs 101, 111) and some others. + + +(20) Styliger and gonostyli. +The posterior-dorsal margin of styliger is distinct, and its postero-ventral margin is not expressed, so the gonostyli are attached on ellipsoid membranous cavities faced ventro-caudally and well visible from ventral view ( +Figs 181 +, +184 +). In other respects styligers and gonostyli are significantly diverse: in + +Petersula + +and + +Kimminsula + +the styliger is short and simple, and the gonostyli retain division into 4 segments ( +Figs 184 +, +376 +, +420 +, +472 +); in + +Ceylonula femoralis + +the styliger is projected medially, and the gonostyli lack boundary between the initial 1st and 2nd segments ( +Fig. 296 +); in + +Hubbardula heterolepida + + +sp. n. + +the styliger is elongated and modified, the membranous cavities of gonostyli attachments are connected medially, and the gonostyli lack boundary between the initial 2nd and 3rd segments ( +Figs 689, 691 +, +698 +). + + + + + +Composition of the + +Kimminsula + +-complex + + + + + +This complex includes two south Indian genera, + +Petersula +Sivaramakrishnan 1984 + +and + +Ghatula + + +gen. n. + +, and three Ceylonese genera, + +Ceylonula + + +gen. n. + +, + +Kimminsula +Peters & Edmunds 1970 + +and + +Hubbardula + + +gen. n. + +Key characters of these genera are given in +Table 1 +. + + + + \ No newline at end of file diff --git a/data/38/0E/87/380E87EFD62A3A1BFF18FE38DD6CCFF9.xml b/data/38/0E/87/380E87EFD62A3A1BFF18FE38DD6CCFF9.xml new file mode 100644 index 00000000000..e0ea7b5f240 --- /dev/null +++ b/data/38/0E/87/380E87EFD62A3A1BFF18FE38DD6CCFF9.xml @@ -0,0 +1,274 @@ + + + +New deep water skates of the genus Notoraja Ishiyama, 1958 (Rajoidei, Arhynchobatidae) from the southwest Pacific + + + +Author + +Séret, Bernard +IRD / Muséum national d’Histoire naturelle, Département Systématique et Évolution, case postale 51, 57, rue Cuvier, F- 75231 Paris cedex 05 (France) seret @ mnhn. fr +seret@mnhn.fr + + + +Author + +Last, Peter R. +Wealth from Oceans Flagship, CSIRO Marine & Atmospheric Research, GPO Box 1538, Hobart, Tasmania 7001 (Australia) peter. last @ csiro. au +last@csiro.au + +text + + +Zoosystema + + +2012 + +2012-06-30 + + +34 + + +2 + + +319 +341 + + + + +http://dx.doi.org/10.5252/z2012n2a9 + +journal article +10.5252/z2012n2a9 +1638-9387 +5165439 + + + + + + +Notoraja longiventralis + +n. sp. + + + + + +( +Figs 16-18 +; +Tables 2 +, +3 +) + + + +Notoraja +sp. 1 + +– Séret +in + +Fricke +et al. +(2011) + +: listed p. 5. + + + + + +HOLOTYPE +. — +MNHN 1999-0449 +, male juvenile +434 mm +TL, +Fiji +, cruise MUSORSTOM 10, +R +/ +V + +Alis + +, +Fiji +, stn CP1361, +18°0’S +, +178°53’E +, 660/ + +666 m +depth + +, + +5.VIII.1998 + +, beam trawl. + + + +PARATYPES +. — +2 specimens +. +MNHN +2008-1389 (field number DHS 402, tissue sample ICTI-001495), male juvenile +229 mm +TL, +MNHN +2008-1388 (field number DHS 401, tissue sample ICTI-001496), newborn male +168 mm +TL, +SANTO +expedition, +R +/ +V +Alis +, +Vanuatu +, NE Tubula Island, stn AT60, +15°33’S +, +167°22’E +, 880/ +953 m +depth, +3.X.2006 +, beam trawl. + + + + +DISTRIBUTION. — On the insular slopes off the +Fiji Islands +, and off Tubula Island ( +Vanuatu +), between 660 and +953 m +depth ( +Fig. 18 +). + + + +ETYMOLOGY. — From the Latin “longi”, long, and “ventralis”, in reference to the very long anterior lobe of the pelvic fin. + + + +DIAGNOSIS. — A species of + +Notoraja + +(probably of medium size) with the following combination of characters: single rudimentary preorbital thorn; dorsal and ventral surfaces of disc entirely velvety, covered with fine denticles; tail long and slender, entirely velvety, without enlarged thorns; lateral tail folds not expanded distally, always narrower than tail width; nasal lobes not greatly expanded, width of nasal curtain 7.6-8.0% TL; mouth relatively broad, its width more than 66% of maximum width of nasal curtain; anterior pelvic-fin lobe longer that posterior lobe; dorsal and ventral surfaces dark, almost uniformly purplish grey; faint whitish spots over pores along the anterior margins of disc; total pectoral-fin radials 64-65, monospondylous centra 26-27, total diplospondylous centra 109-118, total number of centra 135-145. + + + +DESCRIPTION +Disc heart-shaped, 1.13 (1.13) times as broad as long; maximum angle in front of spiracles 92° + +(108°); anterior margin very weakly undulate: slightly concave on either side of tip of snout, convex from anterior extension of propterygium to anterior margin of orbit, concave to level of spiracle; outer corner broadly rounded; posterolateral margin moderately convex. Axis of greatest width 58% (61%) of disc length. Preorbital snout length 3.29 (2.62) times orbit length, 3.65 (3.01) times interorbital width; preoral snout length 1.81 (1.94) times internarial distance. Orbit diameter 1.11 (1.15) times interorbital distance, and 1.53 (2.42) times length of spiracles. Nasal lobes not greatly expanded and rounded, posterior margin shortly and flabby, weakly fringed. Mouth wide, width more than 66% of maximum width of nasal curtain. Upper and lower jaws weakly arched.Teeth plate-like, with short cusps arranged in quincunx in juvenile male +holotype +. Distance between first gill slits 1.60 (1.67) times larger than between nostrils; distance between fifth gill slits 1.07 (1.03) times larger than between nostrils. + + +Pelvic fins deeply incised with lobes connected by radials and membranes; anterior lobe much longer than posterior lobe, finger-like, tapering with pointed tip; posterior lobe with convex lateral margins, posterior margin crenate due to extension of posterior radials. Tail narrow at base, depressed oval over length; strongly convex dorsally, weakly convex ventrally; tapering gradually posteriorly, becoming very slender toward tip; tail width at axils of pelvic fins 2.49 (2.20) times width at midlength of tail, and 3.00 (4.10) times width at dorsal-fin origin respectively; length from rear of cloaca 1.54 (1.58) times distance from tip of snout to rear of cloaca; width 1.48 (1.61) times height at axil of pelvic fin, and width at first dorsal-fin origin 1.29 times height (1.17); lateral skin folds near anterior third of tail, extending to proximal half of epichordal caudal-fin lobe and slightly broadening distally, its width always much less than tail width. Dorsal fins of similar shape and size; flag-like, moderately tall with an evenly convex anterior margin, slightly convex posterior margin and a pointed tip; interdorsal space short, 29% (13%) length of first dorsal-fin base. Epichordal caudal-fin lobe relatively well developed, separated by short interspace from and distinctly shorter than second dorsal-fin base; hypochordal caudal lobe developed, its height about half of that of epichordal lobe, originating near end of lateral fold, confluent with epichordal lobe. Male +holotype +entirely covered with fine dermal denticles on both dorsal and ventral surfaces; denticles densely spaced, bristle-like, with an erect, pointed crown. Single rudimentary preorbital thorn (even in juveniles).Tail uniformly velvety; median thorns rudimentary (barely detectable in juvenile male +holotype +and greatly reduced in smaller juvenile +paratypes +). Malar and alar thorns not developed in +holotype +. + + + +FIG. 16. — + +Notoraja longiventralis + +n. sp. +, holotype (MNHN 1999-0449, male juvenile 434 mm TL): +A +, dorsal surface; +B +, ventral surface. Scale bar: 10 cm. + + + +Tooth rows in upper jaw 38 of +holotype +; +35in +lower jaw.Pectoral propterygial radials +28-29 in +holotype +( +29 in +paratype +); mesopterygial radials 11-12 (12); metapterygial radials 25 (24); total radials 64-65(64). Monospondylous centra 27 (26); diplospondylous predorsal centra 79 (72); predorsal centra 106 (98); caudal centra 39 (37); total diplospondylous centra 118 (109); total centra 145 (135). + + + +FIG. 17. — Dorsal head of + +Notoraja longiventralis + +n. sp. +, holotype (MNHN 1999-0449, male juvenile 434 mm TL). Scale bar: 1 cm. + + + + +FIG. 18.— Oronasal region of + +Notoraja longiventralis + +n.sp. +, holotype (MNHN 1999-0449, male juvenile 434 mm TL). Scale bar: 1 cm. + + + +Colour (in preservative) + +Dorsal and ventral surfaces dark purplish grey, faint whitish spots scattered on ventral surface, mainly at level of pores along the anterior margins of disc. + +Size + + +Reaches at least +434 mm +TL from +holotype +juvenile male; newborn at +168 mm +TL. + + + +REMARKS + + +Notoraja longiventralis + +n. sp. +is set apart from the other velcro skates described above by its much darker dorsal and ventral colouration, its unusually long and pointed anterior pelvic-fin lobes which extend beyond the tip of the posterior lobe, and generally longer interdorsal distance and shorter dorsal head length. + + + + \ No newline at end of file diff --git a/data/38/0E/87/380E87EFD6313A02FF31FA06DE51CFBA.xml b/data/38/0E/87/380E87EFD6313A02FF31FA06DE51CFBA.xml new file mode 100644 index 00000000000..622d6cfba21 --- /dev/null +++ b/data/38/0E/87/380E87EFD6313A02FF31FA06DE51CFBA.xml @@ -0,0 +1,891 @@ + + + +New deep water skates of the genus Notoraja Ishiyama, 1958 (Rajoidei, Arhynchobatidae) from the southwest Pacific + + + +Author + +Séret, Bernard +IRD / Muséum national d’Histoire naturelle, Département Systématique et Évolution, case postale 51, 57, rue Cuvier, F- 75231 Paris cedex 05 (France) seret @ mnhn. fr +seret@mnhn.fr + + + +Author + +Last, Peter R. +Wealth from Oceans Flagship, CSIRO Marine & Atmospheric Research, GPO Box 1538, Hobart, Tasmania 7001 (Australia) peter. last @ csiro. au +last@csiro.au + +text + + +Zoosystema + + +2012 + +2012-06-30 + + +34 + + +2 + + +319 +341 + + + + +http://dx.doi.org/10.5252/z2012n2a9 + +journal article +10.5252/z2012n2a9 +1638-9387 +5165439 + + + + + + +Notoraja inusitata + +n. sp. + + + + + +( +Figs 9-12 +; +Tables 2 +, +3 +) + + + +Notoraja +sp. 2 + +– Séret +in + +Fricke +et al. +(2011) + +: listed p. 5. + + + + + +HOLOTYPE +. — +MNHN 2008-1638 +(field number DHS 733, tissue sample ICTI-001845), male juvenile +444 mm +TL, +SANTO +expedition, +R +/ +V + +Alis + +, +Vanuatu +, +Espiritu + + + +Santo Island, Big Bay, stn 107, +14°58.6’S +, +166°52.5’E +, 807/ +844 m +depth, beam trawl, +16.X.2006 +. + + + + +DISTRIBUTION. — Known only from Big Bay, Espiritu Santo ( +Vanuatu +), from +807 to 844 m +depth ( +Fig. 18 +). + + + + +ETYMOLOGY. — In the absence of an adult male, the generic placement of this ray initially proved to be problematic; its head and disc morphology resemble some species of + +Sinobatis +Hulley, 1973 + +, + +Bathyraja +Ishiyama, 1958 + +and +Insentiraja +. Hence, we have used the Latin “inusitatus” (unusual, strange) to allude to the strange appearance of this ray. + + + + +FIG. 10.— Dorsal head of + +Notoraja inusitata + +n.sp. +,holotype (MNHN 2008-1638, male juvenile 444 mm TL). Scale bar: 1 cm. + + + + +FIG. 11. — Oronasal region of + +Notoraja inusitata + +n. sp. +, holotype (MNHN 2008-1638, male juvenile 444 mm TL). Scale bar: 1 cm. + + + + +DIAGNOSIS. — A species of + +Notoraja + +(probably of medium size as male +440 mm +TL is juvenile) with the following combination of characters: disc broadly heart-shaped, snout tip projecting as a short blunted triangle, single preorbital thorn; dorsal surface of disc entirely velvety, covered with very fine denticles; ventral surface of disc naked; tail long and tapering from base to first dorsal fin, slightly expanded at level of dorsal fins; tail entirely pricked except for the ventral base, an irregular mediodorsal row of small denticles on tail; lateral tail folds expanded at level of dorsal and caudal fins, but width less than tail width; low epichordal caudal-fin lobe; nasal lobes not greatly expanded, width of nasal curtain 7.7% TL; mouth relatively narrow, its width less than 66% of maximum width of nasal curtain and 5.1% TL; anterior and posterior pelvic-fin lobes subequal in length; dorsal surface pale greyish brown, ventral surface whitish. Total pectoral-fin radials 74, monospondylous centra 27, total diplospondylous centra 116, total centra 143. + + + +DESCRIPTION +Disc broadly heart-shaped, 1.10 times as broad as long; maximum angle in front of spiracles 93°; snout tip projecting as a short blunt triangle, rostral cartilage clearly visible dorsally and ventrally, not concealed by thick skin; anterior margin of disc very weakly undulated, slightly and regularly convex from base of snout tip to level of spiracles; outer corner and posterior margins broadly rounded. Axis of greatest width 57% of disc length. Preorbital snout length 3.72 times orbit length, 3.73 times interorbital width; preoral snout length 2.14 times internarial distance. Orbit diameter subequal to interorbital distance, and 1.76 times length of spiracles. Nasal lobes not greatly expanded and rounded, posterior margin weakly and coarsely fringed.Mouth relatively small, its width only about 66% of maximal width of nasal curtain. Upper and lower jaws weakly arched on either side of symphysis. Teeth plate-like, with short cusps and arranged in quincunx. Distance between first gill slits 1.57 times larger than between nostrils; distance between fifth gill slits subequal to internarial distance. +Pelvic fins deeply incised with lobes connected by radials and membranes, anterior lobe long, subequal in length to posterior lobe; posterior lobe with convex lateral margins, posterior margin crenate due to extension of posterior radials. Tail long and tapering from base to first dorsal fin, slightly expanded at level of dorsal fins, then tapering to tail tip; tail only weakly depressed at its base, almost oval in cross-section; more depressed from midlength, only weakly convex ventrally; width at axils of pelvic fins 1.83 times width at midlength of tail, and 2.74 times width at dorsal-fin origin respectively; length from rear of cloaca 1.37 times distance from tip of snout to rear of cloaca; lateral skin folds originating anteriorly to tips of posterior pelvic-fin lobes, extending to distal half to distal fourth of epichordal caudal-fin lobe and broadening distally from about level of first dorsal fin to epichordal lobe of caudal fin; however, fold width less than tail width. Dorsal fins of similar shape and size; rather short and moderately tall with evenly convex anterior margin, straight or slightly convex posterior margin and a pointed tip; separated by an interspace, 52% length of first dorsal-fin base. Epichordal caudal-fin lobe low, separated by short interspace from and distinctly longer than second dorsal-fin base; hypochordal caudal lobe very small, low, originating near end of lateral fold, confluent with epichordal lobe. + + +TABLE 2. — Morphometrics for the holotypes and paratypes of + +Notoraja inusitata + +n. sp. +(MNHN 2008-1638), + +Notoraja fijiensis + +n. sp. +(MNHN 1999-0450 to 453), and + +Notoraja longiventralis + +n. sp. +(MNHN 1999-0449, MNHN 2008-1389). + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+ +N. inusitata +N. longiventralis + +
+ + +Notoraja fijiensis + +n. sp. + + +n. sp. + +n. sp. +
MNHN MNHN MNHN MNHN MNHN MNHN MNHN 1999-0450 1999-0452 1999-0453 1999-0451 2008-1638 1999-0449 2008-1389
femalemale juvenilefemalemale juvenilemale juvenilemale juvenilemale juvenile
holotype paratypeparatypeparatype holotypeholotypeparatype
Total length (mm)386307217212444 434229
Disc width54.149.849.347.652.750.051.5
Disc length (direct)45.944.342.442.947.744.245.4
Snout to maximum width25.926.722.625.527.325.827.5
Snout length (preorbital direct)12.113.213.212.014.511.912.1
Snout to spiracle15.516.215.815.917.315.015.0
Head (dorsal length)18.419.318.318.818.917.617.7
Orbit diameter4.74.14.74.83.93.64.6
Orbit and spiracle length5.14.94.64.94.94.84.9
Spiracle length (main pore)2.32.11.51.82.22.41.9
Distance between orbits3.43.43.73.63.93.34.0
Distance between spiracles6.66.26.16.55.76.06.3
Distance-snout to cloaca38.937.935.037.641.438.538.8
Cloaca to D147.746.947.046.845.945.945.1
Cloaca to D251.051.850.747.249.549.849.9
Cloaca to caudal origin54.455.454.855.752.954.154.6
Distance-cloaca to caudal-fin tip58.560.660.858.556.859.261.1
Ventral snout length (pre upper jaw)13.314.613.215.413.213.2
Prenasal length10.211.410.912.110.410.5
Ventral head length (to fifth gill)24.524.322.923.625.923.623.2
Mouth width6.06.25.75.16.55.0
Distance between nostrils7.16.96.77.27.36.8
Nasal curtain length4.64.23.64.34.34.0
Nasal curtain (total width)8.38.07.37.77.68.0
Nasal curtain (min width)4.75.14.64.64.74.5
Nasal curtain (lobe width)2.11.91.71.81.72.3
Width of first gill opening0.81.00.91.01.10.7
Width of fifth gill opening0.50.60.70.70.90.5
Distance between first gill openings13.311.710.911.311.611.4
Distance between fifth gill openings8.86.37.47.07.87.0
Clasper (post cloacal length)0.06.60.07.36.78.512.0
Length of anterior pelvic lobe13.714.013.715.113.514.815.0
Length of posterior pelvic lobe15.613.212.113.614.012.913.0
Pelvic base width9.47.27.67.77.57.37.9
Tail at axil pelvic fins (width)3.93.02.83.33.43.33.3
Tail at axil pelvic fins (height)2.62.21.82.02.42.22.3
Tail at midlength (width)1.61.51.41.31.81.31.7
Tail at midlength (height)1.31.21.01.11.61.01.3
Tail at D1 origin (width)1.61.11.11.11.21.10.8
+
+ +TABLE 2. — Continuation. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+ +N. inusitata +N. longiventralis + +
+ + +Notoraja fijiensis + +n. sp. + + +n. sp. + +n. sp. +
MNHN MNHN MNHN MNHN MNHN MNHN MNHN 1999-0450 1999-0452 1999-0453 1999-0451 2008-1638 1999-0449 2008-1389
femalemale juvenilefemalemale juvenilemale juvenilemale juvenilemale juvenile
holotype paratype paratype paratypeholotypeholotype paratype
Tail at D1 origin (height)0.80.80.80.70.70.80.6
D1 base length3.23.83.33.83.53.02.6
D1 height1.71.21.21.41.51.31.3
D1 origin to caudal-fin tip10.713.213.614.810.513.014.9
D2 origin to caudal-fin tip7.39.010.810.77.39.29.4
Caudal-fin length4.14.85.66.33.74.94.9
Interdorsal0.30.70.80.80.71.02.0
+
+ +Dorsal surface of disc densely and finely prickled, denticles bristle-like; denticles erect with very slightly curved crowns, on radiate base embedded in skin. A single small, but conspicuous preorbital thorn. Tail prickled dorsally; an irregular mediodorsal row of about 45 small thorns extending from level of pelvic axil to first dorsal-fin origin; thorns with oval, radiate root and a compressed, hooked crown.Ventral surface of disc and pelvic fins totally naked. Ventral surface of tail fined prickled, its base naked. No malar or alar thorns in this juvenile male +holotype +. + + +Tooth rows in upper jaw 41; lower jaw 38. Pectoral propterygial radials 32; mesopterygial radials 16; metapterygial radials 26; total radials 74. Monospondylous centra 27; diplospondylous predorsal centra 81; predorsal centra 108; caudal centra 35; total diplospondylous centra 116; total centra 143. +Colour (in preservative) + +Dorsal surface pale greyish brown; eyes, dorsal-fin and caudal-fin margins, and lateral tail folds darker. Ventral surface whitish, with small pale brownish blotches scattered mainly on outer disc margins and on anterior pelvic lobes; cloaca whitish surrounded by faded brownish markings. + +Size + + +Known only from the juvenile male +holotype +of +440 mm +TL. + +
+ +REMARKS + +Although described from a single juvenile male, this species has distinctive morphological and meristic features that set it clearly apart from its congeners and all other skates of the region. Its general appearance resembles some species of + +Bathyraja + +and Indo-Australian legskates (family +Anacanthobatidae von Bonde & Swart, 1924 +) in having a thin, flabby disc, and long, projecting snout with a narrow, twisted rostral cartilage that is visible both dorsally and ventrally. However, its tail shape is more typical of skates than legskates (thicker, with well-developed dorsal fins, lateral tail folds and denticles). Like other species of + +Notoraja + +, it has a rostral cartilage continuous with chondrocranium, stout proximally but very slender and uncalcified distally ( +Fig. 12 +), broadly oval nasal capsules with basal fenestrae (vs narrow capsules without basal fenestrae in + +Bathyraja + +) and a narrow internasal plate in the chondrocranium (broad in + +Bathyraja + +, see +McEachran & Miyake 1990 +), the precerebral fontanelle is narrow and extends anterior to leading edge of the nasal capsules (vs broad precerebral fontanelle not extending anterior to nasal capsules in + +Bathyraja + +, see McEachan & Dunn 1998), and lower abdominal vertebral counts (27 vs 28-48, rarely fewer than +30 in + +Bathyraja + +; +Stehmann 2005 +). Based on meristic data for 21 species of + +Bathyraja +( +Stehmann, 2005 +) + +, only + +B. richardsoni +(Garrick, 1961) + +has an equally high tooth row count in the upper jaw ( +41 in + +N. inusitata + +n. sp. +and +44 in + +B. richardsoni + +vs +18-36 in +the other 20 species). + +Notoraja inusitata + +n. sp. +can be distinguished from other + +Notoraja +species + +of the region by the features discussed above, its small but distinctly triangular snout tip, naked ventral disc, configuration of the medio-dorsal thorns on the tail, broader lateral tail folds originating at the level of the posterior lobe of the pelvic fin, and more pectoral-fin radials (74 vs 62-66) than its congeners. + + +The genus +Insentiraja +was initially defined as a subgenus of + +Pavoraja +Whitley, 1939 + +by +Yearsley & Last (1992) +for their new species + +P.laxipella + +. It is defined by the absence of thorns on tail and mid-dorsal region of trunk, and presently includes + +I. laxipella + +and + +I. subtilispinosa +( +Stehmann, 1989 +) + +. Our new species bears some resemblance to +Insentiraja +skates (e.g., soft body with loose skin, ventral skin almost transparent) but differs in having a distinct mid-dorsal row of thorns on its tail. Our specimen is a juvenile male and this row might atrophy with growth, but other characters distinguish it from +Insentiraja +skates: e.g., less dense covering of dermal denticles on the dorsal surface of the disc and ventral surface of the tail, greater numbers of precaudal vertebrae (116 vs 95-95) and pectoral radials (74 vs 64-66); see +Yearsley & Last 1992 +and +Ishihara & Stehmann 1990 +. + + +
+
\ No newline at end of file diff --git a/data/38/0E/87/380E87EFD6353A1DFF3BF9C7DCD1CBCF.xml b/data/38/0E/87/380E87EFD6353A1DFF3BF9C7DCD1CBCF.xml new file mode 100644 index 00000000000..91922259d5c --- /dev/null +++ b/data/38/0E/87/380E87EFD6353A1DFF3BF9C7DCD1CBCF.xml @@ -0,0 +1,306 @@ + + + +New deep water skates of the genus Notoraja Ishiyama, 1958 (Rajoidei, Arhynchobatidae) from the southwest Pacific + + + +Author + +Séret, Bernard +IRD / Muséum national d’Histoire naturelle, Département Systématique et Évolution, case postale 51, 57, rue Cuvier, F- 75231 Paris cedex 05 (France) seret @ mnhn. fr +seret@mnhn.fr + + + +Author + +Last, Peter R. +Wealth from Oceans Flagship, CSIRO Marine & Atmospheric Research, GPO Box 1538, Hobart, Tasmania 7001 (Australia) peter. last @ csiro. au +last@csiro.au + +text + + +Zoosystema + + +2012 + +2012-06-30 + + +34 + + +2 + + +319 +341 + + + + +http://dx.doi.org/10.5252/z2012n2a9 + +journal article +10.5252/z2012n2a9 +1638-9387 +5165439 + + + + + + +Notoraja fijiensis + +n. sp. + + + + + +( +Figs 13-15 +; +Tables 2 +, +3 +) + + + + + +HOLOTYPE +. — +MNHN 1999-0450 +, female +386 mm +TL, cruise MUSORSTOM 10, +R +/ +V + +Alis + +, +Fiji +, stn CP1312, + + + +17°24.52’S +, +178°34.00’E +, 660/ +666 m +depth, beam trawl, +5.VIII.1998 +. + + +PARATYPES +. — +3 specimens +. +MNHN +1999-0452, immature male +307 mm +TL, cruise MUSORSTOM 10, +R +/ +V +Alis +, +Fiji +, stn CP1337, +17°3.44’S +, +178°47.21’E +, 635/ +670 m +depth, beam trawl, +9.VIII.1998 +. — +MNHN +1999-0453, female juvenile +217 mm +TL, cruise MUSORSTOM 10, +R +/ +V +Alis +, +Fiji +, stn CP1337, +17°3.44’S +, +178°47.21’E +, 635/ +670 m +depth, beam trawl, +9.VIII.1998 +. — +MNHN +1999-0451, immature male +212 mm +TL, cruise MU- SORSTOM 10, +R +/ +V +Alis +, +Fiji +, stn CP1330, +17°9.50’S +, +178°56.32’E +, 567/ +699 m +depth, beam trawl, +8.VIII.1998 +. + + + + +DISTRIBUTION. — Known from the slope of the +Fiji Islands +, between 567 and +699 m +depth ( +Fig. 18 +). + + + + +ETYMOLOGY. — Based on the +Fiji Islands +where the +type +specimens were collected. + + + + +DIAGNOSIS. — A species of + +Notoraja + +(probably of medium size) with the following combination of characters: a small but conspicuous preorbital thorn; dorsal surface of disc entirely velvety, covered with fine denticles; ventral surface velvety with widely spaced and very fine denticles; tail long and slender, entirely velvety, without enlarged thorns; lateral tail folds not expanded distally, narrower than tail for their whole length; nasal lobes not greatly expanded, width of nasal curtain 7.3-8.3% TL; mouth relatively small, its width more than 66% of maximum width of nasal curtain and 5.7-6.2% TL; anterior pelvic-fin lobe shorter that posterior lobe; dorsal surfaces plain pale yellowish brown, ventral surface creamy white; total pectoral-fin radials 64-66, monospondylous centra 25, total diplospondylous centra 119-127, total number of centra 144-152. + + + +DESCRIPTION + +Disc heart-shaped, 1.18 times as broad as long in +holotype +( +1.11-1.16 in +paratypes +); maximum angle in front of spiracles 98° (91-98°); anterior margin weakly undulate, slightly concave on either side of tip of snout, convex from anterior extension of propterygium to anterior margin of orbit, concave to level of spiracle; outer corner broadly rounded; posterolateral margin moderately convex. Axis of greatest width 56% (53-60%) of disc length. Preorbital snout length 2.56 (2.48-3.26) times orbit length, 3.55 (3.35-3.90) times interorbital width; preoral snout length 1.86 (1.97-2.13) times internarial distance. Orbit diameter 1.39 (1.20-1.35) times interorbital distance, 2.02 (1.96-3.11) times length of spiracles. Nasal lobes not greatly expanded and rounded; posterior margin shortly and flabby fringed. Mouth small, its width more than 66% of maximum width of nasal curtain. Upper and lower jaws weakly arched.Teeth plate-like, with short cusps; arranged in quincunx in female +holotype +and juveniles +paratypes +. Distance between first gill slits 1.86 (1.63-1.70) times longer than distance between nostrils; distance between fifth gill slits 1.23 (0.91- 1.10) times longer than distance between nostrils. Pelvic fins deeply incised with lobes connected by radials and membranes; anterior lobe moderately long, slightly shorter than posterior lobe in +holotype +(longer than posterior lobe in +paratypes +), finger-like, tapering to blunt point distally; posterior lobe with convex lateral margins. Tail narrow at base, oval, depressed slightly, tapering gradually posteriorly; very convex dorsally, weakly convex ventrally; tail width at axil of pelvic fin 2.43 (2.00) times width at midlength of tail, and 2.51 (2.53-2.77) times width at dorsal-fin origin respectively; length from rear of cloaca 1.28 (1.37-1.43) times distance from tip of snout to rear of cloaca; width 1.52 (1.36- 1.51) times height at axil of pelvic fin; width at first dorsal-fin origin 2.03 times height (1.39-1.44); lateral skin folds originating near anterior third of tail, extending to distal third of epichordal caudalfin lobe and broadening distally; fold width always less than tail width. Dorsal fins of similar shape and size; moderately tall, flag-like with evenly convex anterior margin, slightly convex posterior margin and a pointed tip; separated by very short interspace, 10.4% (4.0-5.0%) length of first dorsal-fin base. Epichordal caudal-fin lobe well developed, separated by short interspace from the second dorsal fin, slightly longer than second dorsal-fin base; hypochordal caudal lobe very low, originating near end of lateral fold, confluent with epichordal lobe. + + + +FIG. 12.— Radiograph of the head of + +Notoraja inusitata + +n. sp. +,holotype (MNHN 2008-1638, male juvenile 444 mm TL).Scale bar:1 cm. + + + + +FIG. 13. — + +Notoraja fijiensis + +n. sp. +, holotype (MNHN 1999-0450, female 386 mm TL): +A +, dorsal surface; +B +, ventral surface. Scale bar: 10 cm. + + + + +FIG. 14.— Dorsal head of + +Notoraja fijiensis + +n. sp. +,holotype (MNHN 1999-0450, female 386 mm TL). Scale bar: 1 cm. + + + + +FIG. 15. — Oronasal region of + +Notoraja fijiensis + +n. sp. +, holotype (MNHN 1999-0450, female 386 mm TL). Scale bar: 1 cm. + + + +Dorsal surface entirely covered with fine, bristlelike dermal denticles, with conical bases; denticles partly embedded in skin; crown exposed, erect, slightly curved. Ventral surface less well covered with tiny, very widely spaced denticles (smallest +paratypes +almost naked), their shape similar to those of dorsal surface; belly and pelvic fins mostly devoid of denticles.A conspicuous preorbital thorn. Dorsal and ventral surfaces of tail velvety; dorsal mid line without obvious thorn, instead with an irregular row of slightly enlarged denticles. Malar and alar thorns not developed in female and juvenile male types. + + +Tooth rows in upper jaw +32 in +holotype +( +37-38 in +paratypes +); lower jaw 35 (38-40). Pectoral propterygial radials 29-30 (29); mesopterygial radials 11-12 (11-12); metapterygial radials 23 (23-25); total radials 64 (64-66). Monospondylous centra 25 (25); diplospondylous predorsal centra 80 (77-81); predorsal centra 105 (102-106); caudal centra 41 (38-44); total diplospondylous centra 121 (119- 127); total centra 146 (144-152). + + +Colour (in preservative) + +Dorsal surface plain pale yellowish brown, outer disc margin paler; eyes greyish; midline of tail dusky; dorsal and caudal fins dusky with darker edges; ventral surface of disc and tail creamy white. + +Size + + +Reaches at least +395 mm +TL based on the female +holotype +; a male of +310 mm +TL was still immature. + + + + +REMARKS + +Notoraja fijiensis + +n. sp. +is distinguishable from + +N. alisae + +n. sp. +by its much paler colouration, being pale yellowish brown dorsally (rather than pale greyish brown) and whitish ventrally (rather than dusky yellow), shorter denticles on the dorsal disc, relatively broader predorsal tail, and having larger much darker dorsal fins. Also, it has a more obvious heart-shaped disc with a weakly undulate anterior margin, and its preorbital thorns are more conspicuous. + + + + \ No newline at end of file diff --git a/data/38/0E/87/380E87EFD6393A07FCF9FB63D8ACCCDB.xml b/data/38/0E/87/380E87EFD6393A07FCF9FB63D8ACCCDB.xml new file mode 100644 index 00000000000..a02f2a16db6 --- /dev/null +++ b/data/38/0E/87/380E87EFD6393A07FCF9FB63D8ACCCDB.xml @@ -0,0 +1,920 @@ + + + +New deep water skates of the genus Notoraja Ishiyama, 1958 (Rajoidei, Arhynchobatidae) from the southwest Pacific + + + +Author + +Séret, Bernard +IRD / Muséum national d’Histoire naturelle, Département Systématique et Évolution, case postale 51, 57, rue Cuvier, F- 75231 Paris cedex 05 (France) seret @ mnhn. fr +seret@mnhn.fr + + + +Author + +Last, Peter R. +Wealth from Oceans Flagship, CSIRO Marine & Atmospheric Research, GPO Box 1538, Hobart, Tasmania 7001 (Australia) peter. last @ csiro. au +last@csiro.au + +text + + +Zoosystema + + +2012 + +2012-06-30 + + +34 + + +2 + + +319 +341 + + + + +http://dx.doi.org/10.5252/z2012n2a9 + +journal article +10.5252/z2012n2a9 +1638-9387 +5165439 + + + + + + +Notoraja alisae + +n. sp. + + + + + +( +Figs 1-8 +; +Tables 1 +, +3 +) + + + +Rajidae +NG + +sp. + +– Last +in + +Williams +et al. +2006 + +: listed in appendix 1, p. 36; + +4 colour photos in Appendix 8, p. 6, of female +479 mm +TL ( +NMNZ +P 39619) + +. + + + + + +HOLOTYPE +. — +MNHN 1997-3598 +, adult male +515 mm +TL, cruise HALIPRO 1, +R +/ +V + +Alis + +, stn +CH +876, +northern Norfolk Ridge +, +23°10.41’S +, +166°49.16’E +, + +870 m +depth + +, + +31.III.1994 + +, bottom trawl. + + + +PARATYPES +. — +2 specimens +. +MNHN +1977-3599, male +340 mm +TL, cruise HALIPRO 1, +R +/ +V +Alis +, stn +CH +876, +23°10.41’S +, +166°49.16’E +, +870 m +depth, +31.III.1994 +, bottom trawl.— +MNHN +1997-3600, female +492 mm +TL, cruise HALIPRO 2, +R +/ +V + +Tangaroa + +, stn BT02, northern Norfolk Ridge, +23°16’S +, +167°49’E +, 1025/ +1049 m +depth, +5.XI.1996 +, bottom trawl. + + + + +FIG. 1. — + +Notoraja alisae + +n.sp. +,holotype (MNHN 1997-3598,male adult 515 mm TL): +A +, dorsal surface; +B +, ventral surface.Scale bar:10 cm. + + + + +ADDITIONAL MATERIAL. — 4 dark specimens. MNHN 1997-3601, adult male +533 mm +TL, cruise HALIPRO 2, R/V + +Tangaroa + +, stn BT43, Norfolk Ridge, Seamount “Désespoir”, +25°41’S +, +167°12’E +, 1030/ +1320 m +depth, bottom trawl, +15.XI.1996 +. — MNHN 1997-3597, female +545 mm +TL, MUSORTOM 8, R/V +Alis +, +Vanuatu +, stn CP1008, +18°53.29’S +, +168°52.65’E +, 919/ +1000 m +depth, beam trawl, +25.IX.1994 +. — NMNZ P 39619, female 479 mmTL, NORZANZ cruise, R/V + +Tangaroa + +, stn 155, + + +southern Norfolk Ridge, +34°34.81’S +, +168°57.79’E +, 813/ +1000 m +depth, bottom trawl, +4.VI.2003 +. — MNHN 2003-1780, adult male +460 mm +TL, NORFANZ cruise, R/V + +Tangaroa + +, stn 159, southern Norfolk Ridge, +35°8.13’S +, +169°28.37’E +, 868/ +972 m +depth, bottom trawl, +4.VI.2003 +. + + + + +DISTRIBUTION. — Only known from the northern sector of the Norfolk Ridge (New Caledonian EEZ) from +870 to 1049 m +depth. The dark form exhibits a wider latitudinal distribution, from the southern Norfolk Ridge ( +35°8’S +) in New Zealand’s EEZ to Espiritu Santo in +Vanuatu +( +c. +18°53’S +) ( +Fig. 18 +). + + + + +TABLE 1. — Morphometrics for the pale and dark specimens of + +Notoraja alisae + +n. sp. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+ + +Notoraja alisae + +n. sp. +pale + + + + +Notoraja alisae + +n. sp. +dark + +
MNHN 1997-3598MNHN MNHN 1997-3600 1997-3599MNHN 1997-3601MNHN 1997-3597MNNZ P 39619
male adult holotypefemale paratypemale juvenile male adult paratypefemalefemale
Total length (mm)515492340533545479
Disc width51.755.550.953.755.254.5
Disc length (direct)45.045.743.847.847.746.3
Snout to maximum width25.227.426.028.129.924.4
Snout length (preorbital direct)12.012.311.512.712.412.1
Snout to spiracle15.615.614.516.315.115.3
Head (dorsal length)19.018.817.119.318.518.6
Orbit diameter4.54.04.54.34.24.4
Orbit and spiracle length5.45.45.15.35.15.5
Spiracle length (main pore)1.92.52.12.42.52.6
Distance between orbits3.33.63.73.83.63.5
Distance between spiracles6.46.76.26.56.56.5
Distance-snout to cloaca39.239.437.741.141.740.0
Cloaca to D147.046.148.543.943.744.8
Cloaca to D250.951.052.147.747.949.0
Cloaca to caudal origin58.653.357.951.252.753.3
Distance-cloaca to caudal-fin tip59.657.160.356.856.958.0
Ventral snout length (pre upper jaw)11.713.011.112.312.213.1
Prenasal length10.410.79.810.510.610.9
Ventral head length (to fifth gill)24.324.123.225.523.624.7
Mouth width7.06.56.16.46.76.3
Distance between nostrils7.27.57.07.37.58.0
Nasal curtain length4.14.64.04.94.24.3
Nasal curtain (total width)8.69.28.19.88.88.9
Nasal curtain (min width)4.85.05.05.64.75.3
Nasal curtain (lobe width)2.52.42.12.72.42.3
Width of first gill opening0.91.20.81.41.21.2
Width of fifth gill opening0.71.00.60.91.01.0
Distance between first gill openings10.913.012.411.912.911.9
Length of posterior pelvic lobe15.414.013.616.815.215.0
Pelvic base width8.410.18.08.29.39.8
Tail at axil pelvic fins (width)3.03.73.83.33.53.2
Tail at axil pelvic fins (height)2.02.32.22.12.22.1
Tail at midlength (width)1.21.41.61.41.61.4
Tail at midlength (height)1.21.21.11.11.11.3
Tail at D1 origin (width)1.11.11.01.51.21.1
Tail at D1 origin (height)0.70.80.70.80.70.9
D1 base length2.73.13.43.23.13.7
D1 height1.31.51.01.41.41.4
D1 origin to caudal-fin tip12.010.611.613.013.413.0
D2 origin to caudal-fin tip8.47.27.69.59.48.8
Caudal-fin length4.23.83.45.34.14.4
Interdorsal0.70.91.40.50.90.8
+
+ + +FIG. 2. — Dorsal head of + +Notoraja alisae + +n. sp. +, holotype (MNHN 1997-3598, male adult 515 mm TL). Scale bar: 1 cm. + + + + +FIG. 3.— Oronasal region of + +Notoraja alisae + +n.sp. +,holotype (MNHN 1997-3598, male adult 515 mm TL). Scale bar: 1 cm. + + + + +ETYMOLOGY. — From the name of the French research vessel +Alis +of the Institut de Recherche pour le Développement (IRD) in Nouméa, with which numerous exploratory cruises have been performed in New Caledonian EEZ in the last decades; the name of the ship +Alis +came from the name of a local wind. + + + + +DIAGNOSIS. — A medium-size species of + +Notoraja + +with the following combination of characters:disc wider than long, width 50.9-55.5% TL, length 43.8-45.7% TL; dorsal head length 17.1-19.0% TL; interspiracular distance 6.2-6.7% TL, internasal distance 7.0-8.5% TL, preorbital length 2.7-3.1 times orbit length and 3.4-3.6 interorbital; tail width at pelvic-fin axil 1.5-1.6 times its height; single rudimentary preorbital thorn; dorsal and ventral surfaces of disc entirely velvety, covered with fine denticles; tail long and slender, entirely velvety and without enlarged thorns; lateral tail folds variably expanded posteriorly, their width sometimes greater than tail width at level of second dorsal fin; nasal lobes expanded, width of nasal curtain 8.1-9.8% TL; anterior pelvic-fin lobe shorter that posterior lobe; dorsal and ventral surfaces pale greyish brown; total pectoral-fin radials 63; monospondylous centra 24-25, total diplospondylous centra 112-117, total centra 136-142. + + + +DESCRIPTION + +Disc heart-shaped (more so in adult male than female and young), 1.15 times as broad as long in male +holotype +( +1.16-1.21 in +paratypes +); maximum angle in front of spiracles 83° (98-99°); anterior margin slightly concave on either side of tip of snout, slightly convex from anterior extension of propterygium to anterior margin of orbit, concave to level of spiracle; outer corner broadly rounded; posterolateral margin moderately convex in males; anterolateral margins of disc very slightly undulate in female and juvenile. Axis of greatest width 56% (59-60%) of disc length. Preorbital snout length 2.66 (2.58-3.09) times orbit length, 3.64 (3.11-3.38) times interorbital width; preoral snout length 1.63 (1.58-1.74) times internarial distance. Orbit diameter 1.37 (1.09-1.20) times interorbital distance, and 2.32 (1.59-2.08) times length of spiracles. Nasal lobes moderately expanded and rounded, posterior margin shortly and flabby fringed. Mouth relatively wide, its width more than 66% of maximum width of nasal curtain. Upper jaw of male slightly indented at symphysis (not indented in female and moderately arched); upper and lower jaws slightly arched on either side of symphysis. Teeth with acutely pointed cusps and arranged in parallel rows in mature male +holotype +(plate-like with short cusps and arranged in quincunx in female and juvenile male +paratypes +). Distance between first gill slits 1.51 (1.73-1.77) times larger than distance between nostrils; distance between fifth gill slits 1.00 (1.21-1.29) times larger than distance between nostrils. + + +Pelvic fins deeply incised with lobes connected by radials and membranes, anterior lobe moderately long, reaching to about posterior third of posterior lobe (further in +paratypes +), finger-like with blunt tip; posterior lobe with convex lateral margins, its posterior margin crenate due to extension of posterior radials. Tail narrow at base, variably depressed over length; strongly convex dorsally, slightly convex ventrally; tapering gradually posteriorly; tail width at axils of pelvic fins 2.44 (2.34-2.60) times width at its midlength, 2.65 (3.38-3.71) times its width at dorsal-fin origin respectively; length from rear of cloaca 1.52 (1.45-1.60) times distance from tip of snout to rear of cloaca; width at first dorsal origin 1.53 (1.62-1.71) times height at axils of pelvic fin; width at first dorsal-fin origin 1.73 (1.43- 1.54) times its height; lateral skin folds originating near midlength of tail, extending to distal half of epichordal caudal-fin lobe; folds slightly broadening distally (more so in +paratypes +), but always narrower than tail width. Dorsal fins of similar shape and size; rather short and moderately tall with evenly convex anterior margins, straight or slightly convex posterior margins and a pointed rear tips; separated by a short interspace, 41% (23-36%) length of first dorsal-fin base. Epichordal caudal-fin lobe developed, separated by narrow interspace from and distinctly longer than second dorsal-fin base; hypochordal caudal lobe very low, originating near end of lateral fold, confluent with epichordal lobe. Both dorsal and ventral surfaces entirely covered with fine, densely spaced, dermal denticles; denticles bristle-like, erect, with almost straight pointed crowns. Single greatly reduced preorbital thorn (even very small in juvenile). Tail totally velvety, lacking enlarged thorns; median thorns very small, confined mainly to anterior tail, barely taller than largest denticles adjacent. Alar thorns in three or four irregular rows; posteromedially oriented, with elongated bases, oblique slightly curved crowns, exposed on integument. Malar thorn patch small, on outer anterior margin and merging with those of alar patch; noticeably larger than adjacent denticles, with oval conical base and fine curved cusp. + + + +FIG. 4. — Lateral and dorsal views of tip of tail of: +A +, + +Notoraja alisae + +n. sp. +(holotype MNHN 1997-3598); +B +, + +N. inusitata + +n. sp. +(MNHN 2008-1638); +C +, + +N.fijiensis + +n. sp. +(holotype MNHN 1999-0450); +D +, + +N. longiventralis + +n. sp. +(holotype MNHN 1999-0449).Scale bar:1 cm. + + + + +FIG. 5. — Dorsal dermal denticles of: +A +, + +Notoraja alisae + +n. sp. +(holotype MNHN 1997-3598); +B +, + +N. longiventralis + +n. sp. +(holotype MNHN 1999-0449); +C +, + +N. fijiensis + +n. sp. +(holotype MNHN 1999-0450); +D +, + +N. inusitata + +n. sp. +(MNHN 2008-1638). Scale bars: 1 cm. + + + + +FIG. 6. — + +Notoraja alisae + +n. sp. +, dark form (MNHN 1997-3601, male adult 533 mm TL): +A +, dorsal surface; +B +, ventral surface. Scale bar: 10 cm. + + + + +FIG. 7. — Dorsal head of + +Notoraja alisae + +n. sp. +, dark form (MNHN 1997-3601, male adult 533 mm TL). Scale bar: 1 cm. + + + + +FIG. 8.— Oronasal region of + +Notoraja alisae + +n.sp. +,dark form (MNHN 1997-3601, male adult 533 mm TL). Scale bar: 1 cm. + + + +Claspers long and very slender, glans depressed, but little expanded; with inner dorsal components slit, cleft and pseudorhipidion, and inner ventral components pela, projection and spike. Claspers partially covered with lines of very fine dermal denticles. Tooth rows in upper jaw +38 in +male +holotype +( +34-43 in +paratypes +); lower jaw 40 (33-38). Pectoral propterygial radials 28 (28); mesopterygial radials 11-12 (11-12); metapterygial radials 22-23 (21-24); total radials 62 (61-63). Monospondylous centra 24 (24-25); diplospondylous predorsal centra 77 (78-82); predorsal centra 101 (102-107); caudal centra 35 (35-37); total diplospondylous centra 112 (115-117); total centra 136 (139-142). + + +Colour (in preservative) + +Dorsal surface plain pale greyish brown. Ventral surface lighter, yellowish with faint whitish spots at level of pores of the lateral line system. + +Size + + +Males reach at least +515 mm +TL (adult male +holotype +), and females to at least +545 mm +TL (based on dark female from +Vanuatu +, MNHN 1997-3597). + + + + +REMARKS This velcro skate is well represented by specimens. A group of unusually dark individuals are tentatively assigned to + +Notoraja alisae + +n. sp. +, but were excluded from the +type +series (cf. additional material; +Figs 6-8 +; +Tables 1 +, +3 +)pending further investigation.They closely resemble the typical pale form of this species, except for their darker colouration and slight morphometric differences.These dark specimens are: darker dorsally (plain dark greyish with darker eyes, posterior pelvicfin lobes and lateral tail folds); the ventral surface is dark grey, particularly on the central part of disc; their pale ventral pores are more pronounced, forming lines of light spots along branches of the lateral line system; their disc is slightly longer (46.6-47.8% TL vs 43.8-45.7% TL); precloacal length slightly longer (40.0-41.7% TL vs 37.7-39.4% TL); tail somewhat shorter (distance from the cloaca to the first dorsal-fin origin 43.7-44.8%TL vs 46.1-48.5% TL, to the second dorsal-fin origin 47.7-49.0%TL vs 50.9-52.1%TL, to the caudal-fin origin 51.2-53.3% TL vs 53.3-58.6% TL, and to tail tip 56.8-58.0% TL vs 57.1-60.3%TL). Although the tail is shorter, its predorsal length is longer (distance first dorsal-fin origin to tip of tail 4.1-5.3% TL vs 3.4-4.2% TL). No meristic differences nor differences in the external components of the clasper were found. + + +Squamation is similar in both pale and dark specimens, however a dark mature male (MNHN 1997- 3601) has coarser dermal denticles arranged in small, irregular patches and lines (similar, but less pronounced, lines are present on the posterior pectoral fins of the +holotype +), and the preorbital thorns are not apparent in a dark female (MNHN 1997-3597). Pending collection and examination of more specimens of the dark form, we consider these slight differences to be intraspecific variations of + +N. alisae + +n. sp. + + +
+
\ No newline at end of file diff --git a/data/38/0F/33/380F335206E719ABCE5435054854F98E.xml b/data/38/0F/33/380F335206E719ABCE5435054854F98E.xml new file mode 100644 index 00000000000..b26a711393b --- /dev/null +++ b/data/38/0F/33/380F335206E719ABCE5435054854F98E.xml @@ -0,0 +1,70 @@ + + + +Checklist of bees (Hymenoptera: Apoidea) from small diversified vegetable farms in south-western Montana + + + +Author + +Delphia, Casey M. + + + +Author + +Griswold, Terry + + + +Author + +Reese, Elizabeth G. + + + +Author + +O'Neill, Kevin M. + + + +Author + +Burkle, Laura A. + +text + + +Biodiversity Data Journal + + +2019 + +7 + + +30062 +30062 + + + + +http://dx.doi.org/10.3897/BDJ.7.e30062 + +journal article +http://dx.doi.org/10.3897/BDJ.7.e30062 +1314-2828--30062 + + + + +Nomada ruficornis group sp. F10 + + + +Notes +Unidentate; Table 1: Sites 2, 4. + + + \ No newline at end of file diff --git a/data/38/0F/5E/380F5E5705725084831702C702A2202D.xml b/data/38/0F/5E/380F5E5705725084831702C702A2202D.xml new file mode 100644 index 00000000000..0c10d3d76a2 --- /dev/null +++ b/data/38/0F/5E/380F5E5705725084831702C702A2202D.xml @@ -0,0 +1,374 @@ + + + +Review of the European Eumenes Latreille (Hymenoptera, Vespidae) using morphology and DNA barcodes, with an illustrated key to species + + + +Author + +van Achterberg, Cornelis +https://orcid.org/0000-0002-6495-4853 +Naturalis Biodiversity Center, P. O. 9517, 2300 RA Leiden, Netherlands +kees@vanachterberg.org + + + +Author + +Smit, John T. +https://orcid.org/0000-0002-1568-5183 +Naturalis Biodiversity Center, P. O. 9517, 2300 RA Leiden, Netherlands & European Invertebrate Survey - Netherlands, P. O. 9517, 2300 RA Leiden, Netherlands + + + +Author + +Ljubomirov, Toshko +Institute of Biodiversity and Ecosystem Research, Bulgarian Academy of Sciences, Tzar Osvoboditel Boulevard 1, 1000 Sofia, Bulgaria + +text + + +ZooKeys + + +2023 + +2023-01-31 + + +1143 + + +93 +163 + + + + +http://dx.doi.org/10.3897/zookeys.1143.94951 + +journal article +http://dx.doi.org/10.3897/zookeys.1143.94951 +1313-2970-1143-93 +9156C6A84BF5472FA7010C2F089CE134 +5E978E6177BE5B39B380B105500D7DA5 + + + + +Eumenes mediterraneus Kriechbaumer, 1879 sensu lato + + + + +Figs 94-102 +, 103-111 + + + + +Eumenis +(sic!) +Eumenes mediterraneus +Kriechbaumer, 1879: 85. + + +Eumenes (Eumenes) mediterraneus mediterraneus +; +van der Vecht and Fischer 1972 +: 129 (literature before 1972); +Castro 1992 +: 25, +1997 +: 4; +Dal Pos et al. 2022 +: 15. + + +Eumenes (Eumenes) mediterraneus +; +Frommer 2012 +: 176-182; +Fateryga 2017 +: 182, +2018 +: 206-207. + + +Eumenes mediterraneus +; +Tobias and Kurzenko 1978 +: 160; +Giordani Soika and Borsato 1995 +: 7; +Arens 2012 +: 488; +Neumeyer 2014 +: 367; +2019 +: 271; +Baldock et al. 2020 +: 43; +Cassar et al. 2022 +: 207. + + +Eumenes mediterraneus mediterraneus +; +Borsato and Turrisi 2004 +: 144; +Borsato 2006 +: 142-143; +Castro and Sanza 2009 +: 266; +Gusenleitner 2013 +: 28. + + +Eumenes affinissima race quettaensis +Cameron, 1907: 132-133; +Fateryga 2017 +: 182 (as synonym of +E. mediterraneus +). + + +Eumenes (Eumenes) mediterraneus quettaensis +; +van der Vecht and Fischer 1972 +: 129 (literature before 1972); +Dal Pos et al. 2022 +: 15. + + +Eumenes (Eumenes) mediterraneus quettaensis +; +Gusenleitner 2013 +: 28. + + +Labus superbus +Meade-Waldo, 1910: 36; +Fateryga 2017 +: 182 (as synonym of +E. mediterraneus +). + + +Eumenes (Eumenes) mediterraneus superbus +; +van der Vecht and Fischer 1972 +: 130 (literature before 1972). + + +Eumenes mediterraneus bengasinus +Bluethgen +, 1938: 487; +Gusenleitner 2013 +: 27; +Fateryga 2017 +: 182 (as synonym of +E. mediterraneus +). + + +Eumenes (Eumenes) mediterraneus bengasinus +; +van der Vecht and Fischer 1972 +: 129; +Dal Pos et al. 2022 +: 15. + + +Eumenes mediterraneus cypricus +Bluethgen +, 1938: 488; +Gusenleitner 2013 +: 27; +Fateryga 2017 +: 182 (as synonym of +E. mediterraneus +). + + +Eumenes (Eumenes) mediterraneus cypricus +; +van der Vecht and Fischer 1972 +: 129; +Dal Pos et al. 2022 +: 15. + + +Eumenes (Eumenes) houskai +Giordani Soika, 1952a: 17; +van der Vecht and Fischer 1972 +: 128; +Fateryga 2017 +: 182 (as synonym of +E. mediterraneus +). + + +Eumenes (Eumenes) mediterraneus anatolicus +Giordani Soika, 1952b: 376; +van der Vecht and Fischer 1972 +: 129; +Fateryga 2017 +: 182 (as synonym of +E. mediterraneus +). + + +Eumenes mediterraneus manchurianus +Giordani Soika, 1971: 70; +Gusenleitner 1999 +: 572; +Fateryga 2017 +: 182 (as synonym of +E. mediterraneus +). + + +Eumenes (Eumenes) mediterraneus manchurianus +; +Dal Pos et al. 2022 +: 15. + + +Eumenes mediterraneus var. opacus +Gusenleitner, 1972: 92; +Fateryga 2017 +: 182 (as synonym of +E. mediterraneus +). + + +Eumenes mediterraneus filitosa +Gereys, 2011: 224-225, 2016: 132; +Frommer 2012 +: 179. + + + +Notes. + +This species is in need of a critical revision; the few molecular data indicate that several cryptic species may be included under + +E. mediterraneus + +(Fig. +3 +). The lectotype male of + +E. mediterraneus + +originates from Croatia (Dalmatia) and was examined digitally by photographs kindly supplied by Stephan and Olga Schmidt (ZSM). It has the apical hook of the antenna less curved than pictured in Fig. +111 +and its basal half densely setose. The sampled specimens from Crete and Corsica are different (Fig. +3 +) and a large-scale revision with sufficient fresh material from all over Europe is needed to sort out the relationships within the + +E. mediterraneus + +complex. For the populations of Corsica and Sardinia the name of + +E. m. filitosa + +Gereys is available; supposed to differ in most cases by the entirely black fifth tergite or largely so because of one or more small yellow patch(es) (in + +E. mediterraneus + +usually with complete yellow apical band, but absent in figured typical + +E. mediterraneus + +(Fig. +94 +)). Possibly the strongly convex second metasomal tergite and deeper subposterior depression may be of importance for its separation. For the population of Cyprus ssp. +Eumenes mediterraneus cypricus +Bluethgen +is available and differs by having the punctures of vertex, mesoscutum and second metasomal tergite at least twice larger than in typical + +E. mediterraneus + +( +Gusenleitner 1972 +). + + + +Figures 94-102. + +Eumenes mediterraneus + +Kriechbaumer, Bulgaria, female +94 +metasoma lateral +95 +first metasomal tergite dorsal +96 +first tergite ventral +97 +mesosoma dorsal +98 +antenna anterior +99 +hind tarsus and tarsal claws +100 +head anterior +101 +head and propleuron lateral +102 +propodeum dorsal. + + + + +Figures 103-111. + +Eumenes mediterraneus + +Kriechbaumer, Bulgaria, male +103 +metasoma lateral +104 +first metasomal tergite dorsal +105 +first tergite ventral +106 +head and mesosoma dorsal +107 +propodeum dorsal +108 +head anterior +109 +head and mesosoma lateral +110 +antenna anterior +111 +apical hook of antenna lateral. + + + + +Distribution. + +Mediterranean, Balkan Peninsula, rarely in Central Europe (e.g., Switzerland only in Ticino and Valais and late in season (July-October; +Neumeyer 2019 +) and very rarely collected in Germany ( +Frommer 2012 +; +Reder 2022 +). In Greece starting in April and present in lowland and submontane habitats ( +Arens 2012 +). Reported from Asia up to Turkey, Iran, Afghanistan, Saudi-Arabia, China, Korea, and India, but this probably will change after a full revision (including molecular research) considering the uncertainty about the number of taxa under + +E. mediterraneus + +in Europe. + + + + \ No newline at end of file diff --git a/data/38/0F/7D/380F7DB517CF9769EB3FA0D6C3E643E3.xml b/data/38/0F/7D/380F7DB517CF9769EB3FA0D6C3E643E3.xml new file mode 100644 index 00000000000..bacf56e8281 --- /dev/null +++ b/data/38/0F/7D/380F7DB517CF9769EB3FA0D6C3E643E3.xml @@ -0,0 +1,58 @@ + + + +Checklist of British and Irish Hymenoptera - aculeates (Apoidea, Chrysidoidea and Vespoidea) + + + +Author + +Else, George R. + + + +Author + +Bolton, Barry + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8050 +8050 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8050 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8050 +1314-2828-4-8050 + + + + +Epyris niger Westwood, 1832 + + + +Distribution +England + + + \ No newline at end of file diff --git a/data/38/0F/A0/380FA045FF82FF82FF1AF31CF94F9516.xml b/data/38/0F/A0/380FA045FF82FF82FF1AF31CF94F9516.xml new file mode 100644 index 00000000000..316a22df05e --- /dev/null +++ b/data/38/0F/A0/380FA045FF82FF82FF1AF31CF94F9516.xml @@ -0,0 +1,274 @@ + + + +A taxonomic revision of the Indian species of the ‘ Aterinervis’ group of Culicoides Latreille Subgenus Hoffmania Fox (Diptera: Ceratopogonidae) + + + +Author + +Sarkar, Ankita +0009-0005-2433-2661 +ankitasarkar 785 @ gmail. com; https: // orcid. org / 0009 - 0005 - 2433 - 2661 +ankitasarkar785@gmail.com + + + +Author + +Banerjee, Paramita +0009-0009-5269-3148 +banerjeeparamita 19 @ gmail. com; https: // orcid. org / 0009 - 0009 - 5269 - 3148 +banerjeeparamita19@gmail.com + + + +Author + +Sinha, Shuvra Kanti +0000-0002-2408-7441 +Department of Zoology, Sreegopal Banerjee College, Bagati, Mogra, Hooghly, 712148, West Bengal, India. suvrosinha @ gmail. com; https: // orcid. org / 0000 - 0002 - 2408 - 7441 +suvrosinha@gmail.com + + + +Author + +Mazumdar, Abhijit +0000-0002-2606-9888 +abhijitbu 02 @ gmail. com; https: // orcid. org / 0000 - 0002 - 2606 - 9888 +abhijitbu02@gmail.com + +text + + +Zootaxa + + +2023 + +2023-03-30 + + +5258 + + +4 + + +405 +428 + + + + +http://dx.doi.org/10.11646/zootaxa.5258.4.3 + +journal article +10.11646/zootaxa.5258.4.3 +1175-5326 +7784423 +69D47660-62BF-4E0F-A8D1-B9B27A0051FA + + + + + + + +Culicoides aterinervis +Tokunaga + + + + + + + +( +Fig. 2a–g +) + + + + + + + +Culicoides aterinervis +Tokunaga 1937: 312–315 + + +; + +Arnaud 1956: 95–96 + +; + +Kitaoka 1980: 20 + +; + + +Yu +et al. +2005: 995–996 + + +Diagnosis +(Modified after +Tokunaga 1937 +; +Arnaud 1956 +; +Kitaoka 1980 +and + +Yu +et al. +2005 + +). Pale spot over r-m crossvein continuing as long pale streak parallel to vein M +1 +; narrow, long pale streak along full length of cell m +2 +; broad dark spots between pale area of anal angle and distal pale spots in anal cell. + + + + + +FIGURE 2. + +Culicoides aterinervis + +. a) head; b) third palpal segment; c) hind tibial spines; d) wing; e) spermatheca; f) male genitalia and g) paramere + + + + +Female. + + +Head +( +Figs. 2a and 2b +). Eyes bare, contiguous for 2 facets. Antenna with SCo on flagellomeres 1, 9–13; third palpal segment long, slender, swollen medially, gradually tapering towards apex without sensory pit, numerous scattered capitate sensilla; mandible with 14 teeth. + + +Thorax. +Brown scutum. Postscutellum, scutellum dark brown. + + +Legs +( +Fig. 2c +). Brown; fore femora with apical bands, mid femora with basal, apical pale bands, fore and mid tibiae with basal pale bands, hind femora with basal pale bands, hind tibiae distinctly pale on both ends; hind tibial comb with 5–6 spines, second one longest. + + +Wing +( +Fig. 2d +). Base of wing including anal corner pale; pale spot over r-m cross vein narrow, extending over proximal half of cell r +1 +, crossing vein M; 1 +st +and 2 +nd +radial cells unequal; poststigmatic pale spot broadly covering 2 +nd +radial cell, tapering posteriorly to end before vein M +1 +; pale spot in cell r +3 +not reaching wing margin; proximal pale spots of cells m +1 +and m +2 +confluent; distal pale spot in cell m +1 +elongate, not reaching wing margin; distal pale spot in cell m +2 +broadly meeting wing margin; narrow, long pale streak along the full length of cell m +2 +; distal pale spot in cell cua +1 +extending to wing margin, separated from vein CuA +1 +, pale spot present anterior to base of Cu fork; anal cell with elongate distal pale spot. Macrotrichia few on distal wing blade. + + +Abdomen +( +Fig. 2e +). Brownish; two spherical spermathecae, brown, with short necks; third spermatheca tubular, rudimentary, small sclerotized ring present. + + +Male. + + +Genitalia +( + +Figs. 2f and +2g + +). Caudomedian excavation shallow, U shaped. Tergum IX without apicolateral processes, posterior margin of tergum IX ending before the apex of the gonocoxite; gonocoxite with well developed dorsal root; gonostylus elongate, medially curved with blunt tip. Aedeagus V shaped with small, bent basal arms, stem broad in basal half, tapering to rounded apex. Parameres separated with stout basal arms, stem broad basally, short, slender distally with minute fringing setae. + + +Immatures. +Unknown + + +Larval habitat. +Unknown + + + + +Distribution. +Japan +, +China + + + + +Remarks. + +C. aterinervis + +possessing characters of subgenus + +Hoffmania +( +Wirth & Hubert 1989 +) + +viz., eyes bare, contiguous; SCo on flagellomeres 1, 9–13; second hind tibial spine long; wing with 1 +st +and 2 +nd +radial cell unequal; 2 +nd +radial cell long, broad, at least distal half included in poststigmatic pale spot, proximal pale spots in cell m +1 +and m +2 +confluent; spermathecae two, ovoid with neck, third one rudimentary, a sclerotized ring present; male genitalia rounded without apicolateral processes; gonostylus usually with rounded, blunt tip; gonocoxite with dorsal root; aedeagus usually with basal arch low and the anterior margin often with sclerotized rim, distal process slender, usually with internal sclerotized peg at base; parameres separated with short basal arm, short, slender distally with minute fringing setae. So, it can be stated that this species belong to + +Hoffmania + +rather than + +Culicoides + +and transferred this species to subgenus + +Hoffmania + +. + + + + \ No newline at end of file diff --git a/data/38/0F/A0/380FA045FF82FF84FF1AF07CFE78974F.xml b/data/38/0F/A0/380FA045FF82FF84FF1AF07CFE78974F.xml new file mode 100644 index 00000000000..219303e2082 --- /dev/null +++ b/data/38/0F/A0/380FA045FF82FF84FF1AF07CFE78974F.xml @@ -0,0 +1,163 @@ + + + +A taxonomic revision of the Indian species of the ‘ Aterinervis’ group of Culicoides Latreille Subgenus Hoffmania Fox (Diptera: Ceratopogonidae) + + + +Author + +Sarkar, Ankita +0009-0005-2433-2661 +ankitasarkar 785 @ gmail. com; https: // orcid. org / 0009 - 0005 - 2433 - 2661 +ankitasarkar785@gmail.com + + + +Author + +Banerjee, Paramita +0009-0009-5269-3148 +banerjeeparamita 19 @ gmail. com; https: // orcid. org / 0009 - 0009 - 5269 - 3148 +banerjeeparamita19@gmail.com + + + +Author + +Sinha, Shuvra Kanti +0000-0002-2408-7441 +Department of Zoology, Sreegopal Banerjee College, Bagati, Mogra, Hooghly, 712148, West Bengal, India. suvrosinha @ gmail. com; https: // orcid. org / 0000 - 0002 - 2408 - 7441 +suvrosinha@gmail.com + + + +Author + +Mazumdar, Abhijit +0000-0002-2606-9888 +abhijitbu 02 @ gmail. com; https: // orcid. org / 0000 - 0002 - 2606 - 9888 +abhijitbu02@gmail.com + +text + + +Zootaxa + + +2023 + +2023-03-30 + + +5258 + + +4 + + +405 +428 + + + + +http://dx.doi.org/10.11646/zootaxa.5258.4.3 + +journal article +10.11646/zootaxa.5258.4.3 +1175-5326 +7784423 +69D47660-62BF-4E0F-A8D1-B9B27A0051FA + + + + + + +Subgenus + +Hoffmania + + + + + + + + +Diagnosis (modified after +Wirth & Hubert, 1989 +). + +Eyes bare, usually contiguous. Female antenna with sensilla coeloconica on flagellomeres 1, 9–13. Second hind tibial spine long, 1 +st +and 2 +nd +radial cell unequal; 2 +nd +radial cell long, broad, at least distal half included in poststigmatic pale spot; proximal pale spots in cell m +1 +and m +2 +confluent; base of Cu fork often pale bordered. Two ovoid spermatheca, tubular rudimentary one with short necks; sclerotized ring present. Male genitalia with small or without apicolateral processes. Gonocoxite with dorsal root; ventral root absent. Gonostylus curved usually with rounded or hooked tip. Aedeagus usually with basal arm and anterior margin often with sclerotized rim, narrow stem and slender distally. Parameres with short basal arm often joined medially and distally with minute fringing setae. + + +Aterinervis group +Majumdar1972:40 +;Majumdar & Das Gupta, +in +Majumdar, Das Gupta & Gangopadhyay1997:29 + + +Included species: + +Culicoides aterinervis + +; + +C. isoregalis + +; + +C. neoregalis + +; + +C. pararegalis + +; + +C. pseudoregalis + +; + +C. quasiregalis + +; + +C. regalis + +; + +C. subregalis + + + +Diagnosis. +The following features distinguish species in the Aterinervis Group from all other species of +C. +subg. + +Hoffmania + +: + + +Medium to large size. Basal half of proximal flagellomeres whitish, distal half brownish, distal segments brown. Third palpal segment without sensory pit, scattered sensilla on palpal segments. Fore femora with apical bands, mid femora with basal, apical pale bands, fore and mid tibiae with basal pale bands, hind femora with basal pale bands, hind tibiae pale on both ends. Spur tip frayed. Wing with pale spot over r-m crossvein meeting anterior wing margin and including proximal half of 1 +st +radial cell, distally extending to cell m. Macrotrichia scant. Halter pale. Cerci whitish, discoidal. Parameres separate, terminating in a filamentous spinose tip with 3–4 fringing setae. + + + + \ No newline at end of file diff --git a/data/38/0F/A0/380FA045FF84FF80FF1AF1A7FA8493A6.xml b/data/38/0F/A0/380FA045FF84FF80FF1AF1A7FA8493A6.xml new file mode 100644 index 00000000000..cbe60619ebd --- /dev/null +++ b/data/38/0F/A0/380FA045FF84FF80FF1AF1A7FA8493A6.xml @@ -0,0 +1,253 @@ + + + +A taxonomic revision of the Indian species of the ‘ Aterinervis’ group of Culicoides Latreille Subgenus Hoffmania Fox (Diptera: Ceratopogonidae) + + + +Author + +Sarkar, Ankita +0009-0005-2433-2661 +ankitasarkar 785 @ gmail. com; https: // orcid. org / 0009 - 0005 - 2433 - 2661 +ankitasarkar785@gmail.com + + + +Author + +Banerjee, Paramita +0009-0009-5269-3148 +banerjeeparamita 19 @ gmail. com; https: // orcid. org / 0009 - 0009 - 5269 - 3148 +banerjeeparamita19@gmail.com + + + +Author + +Sinha, Shuvra Kanti +0000-0002-2408-7441 +Department of Zoology, Sreegopal Banerjee College, Bagati, Mogra, Hooghly, 712148, West Bengal, India. suvrosinha @ gmail. com; https: // orcid. org / 0000 - 0002 - 2408 - 7441 +suvrosinha@gmail.com + + + +Author + +Mazumdar, Abhijit +0000-0002-2606-9888 +abhijitbu 02 @ gmail. com; https: // orcid. org / 0000 - 0002 - 2606 - 9888 +abhijitbu02@gmail.com + +text + + +Zootaxa + + +2023 + +2023-03-30 + + +5258 + + +4 + + +405 +428 + + + + +http://dx.doi.org/10.11646/zootaxa.5258.4.3 + +journal article +10.11646/zootaxa.5258.4.3 +1175-5326 +7784423 +69D47660-62BF-4E0F-A8D1-B9B27A0051FA + + + + + + + +Culicoides isoregalis +Majumdar & Das Gupta + + + + + + + +( +Fig 3a–i +) + + + + + + +Culicoides isoregalis +Majumdar & Das Gupta + +, +in + +Majumdar, Das Gupta & Gangopadhyay 1997: 28 + +; + +Majumdar 1972: 143–147 + +; + +Nandi 2014: 88–90 + + + + + + +Material examined. +Holotype +( +1 ♀ +), Darjeeling Govt. College, August, 1968, Coll. P.K. Chaudhuri; +Allotype +(1 ♁), Darjeeling Govt. College, May, 1968, Coll. P.K. Chaudhuri. + + + + +Diagnosis. +The only species in the Aterinervis group with the following suite of characters: Poststigmatic pale spot not extending posteriorly to touch but not cross vein M +1 +; distal pale spot in cell m +1 +narrow, elongate; triangular pale spot in cell cua +1 +; anal cell with elongate distal pale spot; posterior margin of tergum IX ending just before the apex of the gonocoxite. + + +Female. + + +Head +( +Figs. 3a, 3b and 3c +). Antenna with SCo on flagellomeres 1, 9–13. Third palpal segment slender, medially swollen bearing capitate sensilla without sensory pit; second segment slender, first, fourth, fifth segments short, stout. + + + +FIGURE 3. + +Culicoides isoregalis +. + +a) head; b) mandibular teeth; c) maxillary palp; d) hind tibial spines; e) mid tarsis; f) wing; g) spermathecae with ring; h) male genitalia and i) paramere + + + +Thorax. +Scutum pale brown; lateral margin dark brown with two dark lateral, pale median streaks; postscutellum dark brown. + + +Legs +( +Figs. 3d and 3e +). Brownish; fore femora with pale apical and mid femora with basal and apical pale bands, fore and mid tibiae with basal pale bands, hind femora with pale basal bands, hind tibia with pale basal and apical bands; hind tibial comb with 6 spines, second longest; spur tip frayed; claws equal. + + +Wing +( +Fig. 3f +). Pale spot over r-m crossvein crossing vein M; distal portion of 2 +nd +radial cell included in pale triangular poststigmatic pale spot that does not extend to vein M +1 +; apical pale spot in cell r +3 +not reaching wing margin; cell m +1 +with two pale spots, distal one elongate, not reaching wing margin; distal pale spot in cell m +2 +broadly reaching wing margin; triangular pale spot in cell cua +1 +expanded at wing margin; dark spot parallel with vein CuA +2 +; dark marking in anal angle; distal pale spot broadly tapering to posterior wing margin. Macrotrichia numerous on distal part of the wing. + + +Abdomen +( + +Fig. +3g + +). Dark streaks on terga; spermatheca two, subequal, ovoid, well developed, brown with sclerotized, oblique necks; rudimentary spermatheca present; small ring present. + + +Male. +Similar to female with usual sexual differences. + + +Genitalia +( +Figs. 3h and 3i +). Caudomedian excavation shallow, U shaped. Tergum IX without apicolateral processes, posterior margin of tergum IX ending before the apex of the gonocoxite; gonocoxite with well developed dorsal root; gonostylus elongate, medially curved with blunt tip. Aedeagus V shaped with small, bent basal arms, stem broad at basal half, narrow end. Parameres with stout basal arms, stem broad basally. + + +Immatures. +Unknown + + +Larval habitat. +Unknown + + + + +Distribution. +India +(Darjeeling, +West Bengal +) + + + + +Remarks +. + +C. isoregalis + +is similar to + +C. subregalis + +in possessing dark area at anal angle, pale spot over r-m crossvein narrow. It differs as it possesses an elongate distal pale spot in cell m +1 +, triangular pale spot in cell cua +1 +and a pale brown scutum. These two species share many similarities and have overlapping morphometric data so may in fact be a single, variable species but this requires further validation to confirm. + +C. regalis + +is also similar to + +C. isoregalis + +but differs in antennal ratio, palpal ratio and in the number of mandibular teeth ( +Table 1 +), presence of pale spot over r-m crossvein broad, pale area of wing base extending to posterior wing margin of anal cell and distal pale spot of anal cell bilobed. + + + + \ No newline at end of file diff --git a/data/38/0F/A0/380FA045FF86FF8EFF1AF077FE3991C2.xml b/data/38/0F/A0/380FA045FF86FF8EFF1AF077FE3991C2.xml new file mode 100644 index 00000000000..b0026ac9fa3 --- /dev/null +++ b/data/38/0F/A0/380FA045FF86FF8EFF1AF077FE3991C2.xml @@ -0,0 +1,275 @@ + + + +A taxonomic revision of the Indian species of the ‘ Aterinervis’ group of Culicoides Latreille Subgenus Hoffmania Fox (Diptera: Ceratopogonidae) + + + +Author + +Sarkar, Ankita +0009-0005-2433-2661 +ankitasarkar 785 @ gmail. com; https: // orcid. org / 0009 - 0005 - 2433 - 2661 +ankitasarkar785@gmail.com + + + +Author + +Banerjee, Paramita +0009-0009-5269-3148 +banerjeeparamita 19 @ gmail. com; https: // orcid. org / 0009 - 0009 - 5269 - 3148 +banerjeeparamita19@gmail.com + + + +Author + +Sinha, Shuvra Kanti +0000-0002-2408-7441 +Department of Zoology, Sreegopal Banerjee College, Bagati, Mogra, Hooghly, 712148, West Bengal, India. suvrosinha @ gmail. com; https: // orcid. org / 0000 - 0002 - 2408 - 7441 +suvrosinha@gmail.com + + + +Author + +Mazumdar, Abhijit +0000-0002-2606-9888 +abhijitbu 02 @ gmail. com; https: // orcid. org / 0000 - 0002 - 2606 - 9888 +abhijitbu02@gmail.com + +text + + +Zootaxa + + +2023 + +2023-03-30 + + +5258 + + +4 + + +405 +428 + + + + +http://dx.doi.org/10.11646/zootaxa.5258.4.3 + +journal article +10.11646/zootaxa.5258.4.3 +1175-5326 +7784423 +69D47660-62BF-4E0F-A8D1-B9B27A0051FA + + + + + + + +Culicoides neoregalis +Majumdar & Das Gupta + + + + + + + +( +Fig 4a–i +) + + + + + + +Culicoides neoregalis +Majumdar & Das Gupta + +, +in + +Majumdar, Das Gupta & Gangopadhyay 1997: 29 + +; + +Majumdar 1972: 161–165 + +; + +Nandi 2014: 90–92 + + + + + + +Materials examined. +Holotype +( +1 ♀ +), Darjeeling Govt. College. +02.vi.1968 +, Coll. Dr. P.K. Chaudhuri; +Allotype +(1 ♁), Darjeeling Govt. College, +04.ix.1968 +, Coll. P.K. Chaudhuri. + + + + +Diagnosis. +Pale spot over r-m cross vein broad, extending posteriorly to cell m +2 +; broad dark band apical to r-m crossvein, straddling vein M continuous to cell m +1 +; distal pale spot in cell r +3 +broad reaches apex of cell, confluent with distal pale spot of cell m +1 +and m +2 +; poststigmatic pale spot crossing vein M +1 +, confluent with proximal pale spots of cells m +1 +and m +2 +and distal pale spot in cell cua +1; +anal cell with one broadly constricted distal pale spot. + + +Female. + + +Head +( +Figs. 4a and 4b +). Antenna with SCo on flagellomeres 1, 9–13; third palpal segment slender, medially swollen, gradually tapering towards apex with minute capitate sensilla; second palp segment longer than first, fourth and fifth segments, fifth palpal segment with 4 apical sensilla chaetica. + + +Thorax. +Brown; long dark markings on scutum; humeral region pale; postscutellum dark. + + +Legs +( +Figs. 4c and 4d +). Brownish; fore femora with apical bands, mid femora with basal, apical pale bands, fore and mid tibiae with basal pale bands, hind femora with basal pale bands; hind tibia with pale basal and apical bands; hind tibial comb with 6 spines, second one longest; spur tip frayed; claws equal. + + +Wing +( +Fig. 4e +). Brownish with many interconnected pale areas, pale area of wing base extending to posterior margin of anal cell; pale spot over r-m crossvein broad, continuous posteriorly to cell m +2 +; dark spot at the junction of radial cells crossing vein M +1 +; poststigmatic pale spot posteriorly converging with pale area of cell m +1 +; pale spot in cell r +3 +broadly reaching wing margin; pale spot in cell cua +1 +extending to wing margin, touching vein CuA +1 +; one medially constricted distal pale spot in anal cell, anteriorly extending to the stem of Cu fork, posteriorly expanded at posterior wing margin. + + +Abdomen +( +Fig. 4f +). Brownish with dark streaks; lateral margin of sternite VIII straight; spermatheca two, pyriform, equal to subequal, well developed, with a short, oblique scletotized neck, a small sclerotized ring; fingerlike rudimentary spermatheca present. + + +Male. +Similar to female with usual sexual differences. + + +Genitalia +( + +Figs. +4g +, 4h and 4i + +). Sternum IX sclerotized with medially shallow caudomedian excavation; tergum IX with weakly developed apicolateral processes, median cleft present at caudal margin; posterior margin of tergum IX ending beyond the apex of gonocoxite. Gonocoxite stout with well developed dorsal root, more or less narrow distally. Gonostylus broad basally, abruptly curved medially, narrowing to blunt tip.Aedeagus V shaped, represented by two sclerites with stout basal arms, distal process elongated. Parameres with broad basal arms joined at mid portion, narrowing distally with minute fringing setae. + + + +FIGURE 4. + +Culicoides neoregalis +. + +a) maxillary palp; b) mandibular teeth; c) hind tibial spines; d) fore tarsis; e) wing; f) spermathecae with ring; g) male genitalia; h) paramere and i) aedeagus + + + +Immatures. +Unknown + + +Larval habitat. +Unknown + + + + +Distribution. +India +(Darjeeling, +West Bengal +) + + + + +Remarks. + +C. neoregalis + +resembles + +C. regalis + +in retaining pale area of wing base extending to posterior wing margin of anal cell, a constricted distal pale spot in anal cell but + +C. neoregalis + +varies in antennal ratio, palpal ratio, mandibular teeth ( +Table 1 +), larger, coalescing pale areas over wing, distal pale spot in cell r +3 +broadly meeting wing margin, poststigmatic pale spot covering almost 2 +nd +radial cell and crossing vein M +1 +. + +C. pararegalis + +varies from + +C. neoregalis + +by having a reduced distal pale spot in cell r +3 +and two separate, round distal pale spots in anal cell. + + + + \ No newline at end of file diff --git a/data/38/0F/A0/380FA045FF88FF8EFF1AF593FFF79694.xml b/data/38/0F/A0/380FA045FF88FF8EFF1AF593FFF79694.xml new file mode 100644 index 00000000000..f8aeb42ffa2 --- /dev/null +++ b/data/38/0F/A0/380FA045FF88FF8EFF1AF593FFF79694.xml @@ -0,0 +1,262 @@ + + + +A taxonomic revision of the Indian species of the ‘ Aterinervis’ group of Culicoides Latreille Subgenus Hoffmania Fox (Diptera: Ceratopogonidae) + + + +Author + +Sarkar, Ankita +0009-0005-2433-2661 +ankitasarkar 785 @ gmail. com; https: // orcid. org / 0009 - 0005 - 2433 - 2661 +ankitasarkar785@gmail.com + + + +Author + +Banerjee, Paramita +0009-0009-5269-3148 +banerjeeparamita 19 @ gmail. com; https: // orcid. org / 0009 - 0009 - 5269 - 3148 +banerjeeparamita19@gmail.com + + + +Author + +Sinha, Shuvra Kanti +0000-0002-2408-7441 +Department of Zoology, Sreegopal Banerjee College, Bagati, Mogra, Hooghly, 712148, West Bengal, India. suvrosinha @ gmail. com; https: // orcid. org / 0000 - 0002 - 2408 - 7441 +suvrosinha@gmail.com + + + +Author + +Mazumdar, Abhijit +0000-0002-2606-9888 +abhijitbu 02 @ gmail. com; https: // orcid. org / 0000 - 0002 - 2606 - 9888 +abhijitbu02@gmail.com + +text + + +Zootaxa + + +2023 + +2023-03-30 + + +5258 + + +4 + + +405 +428 + + + + +http://dx.doi.org/10.11646/zootaxa.5258.4.3 + +journal article +10.11646/zootaxa.5258.4.3 +1175-5326 +7784423 +69D47660-62BF-4E0F-A8D1-B9B27A0051FA + + + + + + + +Culicoides pararegalis +Majumdar & Das Gupta + + + + + + + +( +Fig 5a–i +) + + + + + + +Culicoides pararegalis +Majumdar & Das Gupta + +, +in + +Majumdar, Das Gupta & Gangopadhyay 1997: 28 + +; + +Majumdar 1972: 165– 168 + +; + +Nandi 2014: 92–93 + + + + + + +Material examined. + +Holotype +( +1 ♀ +), Darjeeling Govt. College, + +25.vi.1968 + +, +Coll. Dr. S.K. Das Gupta +; +1 ♀ +, PHE camp, +Neora Valley National Park +, + +14.iii.2021 + +, +Coll. S.K. Sinha. + + + + + +Diagnosis. +Pale spot over r-m cross vein broad, extending to cell m +2 +; distal pale spot on cells r +3 +and m +1 +reduced, distant from wing margin; anal cell with two separated distal pale spots. + + +Female. + + +Head +( +Figs. 5a and 5b +). Eyes contiguous, for 3 facets. Antenna with SCo on flagellomeres 1, 9–13; third palpal segment long, slender, numerous capitate sensilla, second segment long, with minute capitate sensilla, first, fourth and fifth segments short, fifth segment with 4 apical sensilla chaetica. + + +Thorax +( +Fig. 5c +). Brown with random dark markings; postscutellum brown. + + +Legs +( +Figs 5d and 5e +). Brownish; fore femora with pale apical bands, mid femora with narrow pale area at base, apex pale, hind femora basally pale, fore and mid tibia with broad pale band in basal half, hind tibia with pale basal and apical bands; hind tibial comb with 6 unequal spines, second one longest; spur tip frayed; claws equal. + + +Wing +( +Fig. 5f +). Pale area at wing base extending to posterior wing margin of anal cell; pale spot over r-m crossvein crossing vein M, continuous to cell m +2 +; a large poststigmatic pale spot including almost entire 2 +nd +radial cell expanded at wing margin, ending posteriorly before vein M +1 +; pale spot in cell r +3 +reduced, not reaching wing margin, closer to vein M +1 +than to wing margin; pale streak parallel to vein M +1 +; cell m +1 +with a distal small, oval pale spot separated from wing margin; cell m +2 +with additional two spots, one overlying over Cu fork, distal one larger, narrowly separated from wing margin; cell cua +1 +with a pale spot extending to posterior wing margin, proximal portion of dark spot over vein CuA +2 +expanded, posteriorly tapered; anal cell with two rounded distal spots. + + +Abdomen ( +Figs. 5h and 5i +). Brownish with dark streaks; spermatheca two, well developed, ovoid, subequal, well sclerotized with short, oblique prominent necks; rudimentary one small, tubular; ring indistinct. + + +Male. +Unknown + + +Immatures. +Unknown + + +Larval habitat. +Unknown + + + + +Distribution. +India +(Darjeeling, Neora Valley National Park, +West Bengal +) + + + + +Remarks. + +C. pararegalis + +similar to + +C. regalis + +as pale area of wing base extending to posterior wing margin of anal cell and with a broad pale spot over r-m crossvein. Additionally, the morphometric data ( +Table 1 +) of these species overlaps suggesting that + +C. pararegalis + +may just be a variant of the more widespread + +C. regalis +. + +The major difference between these species is the reduced distal pale spot in cell r +3 +and two separate distal pale spots in anal cell of + +C. pararegalis + +, warrant further investigation to confirm the status of + +C. pararegalis + +. + + + + \ No newline at end of file diff --git a/data/38/0F/A0/380FA045FF8AFF8BFF1AF4FAFA9B945A.xml b/data/38/0F/A0/380FA045FF8AFF8BFF1AF4FAFA9B945A.xml new file mode 100644 index 00000000000..f99fef4d45c --- /dev/null +++ b/data/38/0F/A0/380FA045FF8AFF8BFF1AF4FAFA9B945A.xml @@ -0,0 +1,263 @@ + + + +A taxonomic revision of the Indian species of the ‘ Aterinervis’ group of Culicoides Latreille Subgenus Hoffmania Fox (Diptera: Ceratopogonidae) + + + +Author + +Sarkar, Ankita +0009-0005-2433-2661 +ankitasarkar 785 @ gmail. com; https: // orcid. org / 0009 - 0005 - 2433 - 2661 +ankitasarkar785@gmail.com + + + +Author + +Banerjee, Paramita +0009-0009-5269-3148 +banerjeeparamita 19 @ gmail. com; https: // orcid. org / 0009 - 0009 - 5269 - 3148 +banerjeeparamita19@gmail.com + + + +Author + +Sinha, Shuvra Kanti +0000-0002-2408-7441 +Department of Zoology, Sreegopal Banerjee College, Bagati, Mogra, Hooghly, 712148, West Bengal, India. suvrosinha @ gmail. com; https: // orcid. org / 0000 - 0002 - 2408 - 7441 +suvrosinha@gmail.com + + + +Author + +Mazumdar, Abhijit +0000-0002-2606-9888 +abhijitbu 02 @ gmail. com; https: // orcid. org / 0000 - 0002 - 2606 - 9888 +abhijitbu02@gmail.com + +text + + +Zootaxa + + +2023 + +2023-03-30 + + +5258 + + +4 + + +405 +428 + + + + +http://dx.doi.org/10.11646/zootaxa.5258.4.3 + +journal article +10.11646/zootaxa.5258.4.3 +1175-5326 +7784423 +69D47660-62BF-4E0F-A8D1-B9B27A0051FA + + + + + + + +Culicoides pseudoregalis +Majumdar & Das Gupta + + + + + + + +( +Fig 6a–h +) + + + + + + +Culicoides pseudoregalis +Majumdar & Das Gupta + +, +in + +Majumdar, Das Gupta & Gangopadhyay 1997: 30 + +; + +Majumdar 1972: 176–180 + +; + +Nandi 2014: 99–100 + + + + + + +Materials examined. + +Holotype +( +1 ♀ +), Darjeeling Govt. College, + +24.viii.1968 + +, +Coll. Dr. S.K. Das Gupta. +1 ♀ +, +Bhotaykhadka +, +Neora Valley National Park +, + +19.x.2019 + +, +Coll. S. K. Sinha. + + + + + +Diagnosis. +Poststigmatic pale spot ended before vein M +1 +; anal cell with two constricted proximal and distal hourglass shaped pale spots. + + +Female. + + +Head +( +Figs. 6a and 6b +). Antenna with SCo on flagellomeres 1, 9–13; first flagellomere whitish at basal half, distal half brown, flagellomeres 2–13 brown. Third palpal segment long, slender with minute capitate sensilla, without sensory pit; first segment short, second segment stout, fourth, fifth segments short, 4 apical sensilla in fifth segment. + + + +FIGURE 6. + +Culicoides pseudoregalis +. + +a) head; b) maxillary palp; c) thorax; d) mid tarsis; e) hind tibial spines; f) wing; g) halter and h) spermathecae with ring + + + +Thorax +( +Fig. 6c +). Brown; scutum with distinct median pale streak; scutellum dark; postscutellum dark brown. + + +Legs +( +Figs. 6d and 6e +). Brownish; fore and mid femora with pale apical bands, mid and hind femora with pale bases, fore and mid tibiae with broad basal bands, hind tibia with apical, basal pale band; hind tibial comb with 5 spines, second one longest; spur tip frayed; claws equal. + + +Wing +( +Fig. 6f +). Grayish; dark area at anal angle; pale spot over r-m crossvein narrow, reaching vein M; poststigmatic pale spot not reaching vein M +1 +; dark band apical to r-m crossvein broadly touching costal margin, continuous posteriorly to cell m +2 +; distal pale spot in cell r +3 +not reaching wing margin; cell m +1 +with an oval, distal pale spot distant from wing margin, dark streaks overlying vein M +1 +, distally with pale streaks; total three pale spots present in cell m +2 +, proximal pale spot present overlying Cu fork, next one confluent with pale spot in cell m +1 +and third distal one touching wing margin; cell cua +1 +with a large triangular pale spot touching wing margin, narrowly separated from vein CuA +2 +, anal cell with two narrowly constricted proximal and distal pale spots. Macrotrichia restricted to apical, posterior wing blade. + + +Abdomen +( +Fig. 6h +). Brownish with dark streaks; two well developed, unequal, oval spermathecae well sclerotized with prominent, straight necks; rudimentary spermatheca more or less bladder-like; sclerotized ring present. + + +Male. +Unknown. + + +Immatures. +Unknown + + +Larval habitat. +Unknown + + + + +Distribution. +India +(Darjeeling, Neora Valley National Park, +West Bengal +) + + + + +Remarks. + +C. pseudoregalis + +is similar in appearance to + +C. quasiregalis + +in having pale area at wing base extending to anal angle and a dark marking in the anal corner but differs slightly in antennal and palpal ratios and two constricted pale spots. These characters may represent intraspecific variability but this requires studying more specimens. This species differs from + +C. neoregalis + +and + +C. regalis + +in possessing a narrow pale spot over r-m crossvein, two narrowly constricted pale spots in anal cell, dark marking in anal corner. It is distinguished from + +C. pararegalis + +by possessing a higher antennal ratio, smaller palpal ratio ( +Table 1 +), hind tibial comb with 5 spines and a large distal pale spot in cell r +3 +. + + + + \ No newline at end of file diff --git a/data/38/0F/A0/380FA045FF8DFF8AFF1AF0EBF92F97F9.xml b/data/38/0F/A0/380FA045FF8DFF8AFF1AF0EBF92F97F9.xml new file mode 100644 index 00000000000..a9d7f8d86b9 --- /dev/null +++ b/data/38/0F/A0/380FA045FF8DFF8AFF1AF0EBF92F97F9.xml @@ -0,0 +1,236 @@ + + + +A taxonomic revision of the Indian species of the ‘ Aterinervis’ group of Culicoides Latreille Subgenus Hoffmania Fox (Diptera: Ceratopogonidae) + + + +Author + +Sarkar, Ankita +0009-0005-2433-2661 +ankitasarkar 785 @ gmail. com; https: // orcid. org / 0009 - 0005 - 2433 - 2661 +ankitasarkar785@gmail.com + + + +Author + +Banerjee, Paramita +0009-0009-5269-3148 +banerjeeparamita 19 @ gmail. com; https: // orcid. org / 0009 - 0009 - 5269 - 3148 +banerjeeparamita19@gmail.com + + + +Author + +Sinha, Shuvra Kanti +0000-0002-2408-7441 +Department of Zoology, Sreegopal Banerjee College, Bagati, Mogra, Hooghly, 712148, West Bengal, India. suvrosinha @ gmail. com; https: // orcid. org / 0000 - 0002 - 2408 - 7441 +suvrosinha@gmail.com + + + +Author + +Mazumdar, Abhijit +0000-0002-2606-9888 +abhijitbu 02 @ gmail. com; https: // orcid. org / 0000 - 0002 - 2606 - 9888 +abhijitbu02@gmail.com + +text + + +Zootaxa + + +2023 + +2023-03-30 + + +5258 + + +4 + + +405 +428 + + + + +http://dx.doi.org/10.11646/zootaxa.5258.4.3 + +journal article +10.11646/zootaxa.5258.4.3 +1175-5326 +7784423 +69D47660-62BF-4E0F-A8D1-B9B27A0051FA + + + + + + + +Culicoides quasiregalis +Majumdar & Das Gupta + + + + + + + +( +Fig 7a–g +) + + + + + + +Culicoides quasiregalis +Majumdar & Das Gupta + +, +in + +Majumdar, Das Gupta & Gangopadhyay 1997: 30 + +; + +Majumdar 1972: 180– 183 + +; + +Nandi 2014:101–102 + + + + + + +Materials examined. +Holotype +( +1 ♀ +), Darjeeling Govt. College, August, 1968, Coll. Dr. S.K. Das Gupta. + + + + +Diagnosis. +Poststigmatic pale spot ended before vein M +1 +; anal cell with two separated proximal pale spots and narrowly constricted distal pale spot. + + +Female. + + +Head +( +Figs 7a and 7b +). Eyes contiguous for 2 facets. Antenna with SCo on flagellomeres 1, 9–13. Third palpal segment long, slender with numerous capitate sensilla, without sensory pit; first, fourth, fifth segments short, stout; second segment long. + + +Thorax +( +Fig. 7c +). Brown; scutum with dark linear streaks; scutellum with 8 bristles; postscutellum brownish. + + +Legs +( +Figs.7d and 7e +). Brownish; fore femora with pale apical bands, mid femora with pale basal and apical bands, hind femora with basal band, fore and mid tibiae with broad pale basal bands, hind tibiae with pale broad basal and apical bands; hind tibial comb with 5 unequal spines, second from spur longest; spur tip frayed; claws equal. + + +Wings +( +Fig. 7f +). A clear dark marking on anal corner; pale spot on r-m crossvein extending distally to vein M; poststigmatic pale spot covering most of 2 +nd +radial cell, not reaching vein M +1 +; a large pale spot in cell r +3 +; cells m +1 +and m +2 +each with two spots; a pale streak bordering vein M +1 +; cell cua +1 +with a triangular pale spot, extending from vein CuA +1 +to wing margin; anal cell with a narrowly constricted distal pale spot. + + +Abdomen +( + +Fig. +7g + +). Brown with dark streaks; two well developed, brown, unequal, ovoid, spermathecae well sclerotized with short necks; rudimentary spermatheca small. + + +Male. +Unknown + + +Immatures. +Unknown + + + +FIGURE 7. + +Culicoides quasiregalis +. + +a) head; b) maxillary palp; c) thorax; d) fore tarsis; e) hind tibial spines; f) wing and g) spermathecae with ring + + + +Larval habitat. +Unknown + + + + +Distribution. +India +(Darjeeling, Kurseong, +West Bengal +) + + + + +Remarks. + +C. quasiregalis + +most closely resembles + +C. pseudoregalis + +as both have grayish wing, hind tibial comb with 5 spines but the two species differ in antennal and palpal ratios ( +Table 1 +) and the presence of a discrete constricted distal pale spot in the anal cell.This character may be variable, assumed to be a variant of + +C. pseudoregalis + +but this requires further investigations. + + + + \ No newline at end of file diff --git a/data/38/0F/A0/380FA045FF8FFF89FF1AF4FAF8C497E4.xml b/data/38/0F/A0/380FA045FF8FFF89FF1AF4FAF8C497E4.xml new file mode 100644 index 00000000000..da31356b69e --- /dev/null +++ b/data/38/0F/A0/380FA045FF8FFF89FF1AF4FAF8C497E4.xml @@ -0,0 +1,303 @@ + + + +A taxonomic revision of the Indian species of the ‘ Aterinervis’ group of Culicoides Latreille Subgenus Hoffmania Fox (Diptera: Ceratopogonidae) + + + +Author + +Sarkar, Ankita +0009-0005-2433-2661 +ankitasarkar 785 @ gmail. com; https: // orcid. org / 0009 - 0005 - 2433 - 2661 +ankitasarkar785@gmail.com + + + +Author + +Banerjee, Paramita +0009-0009-5269-3148 +banerjeeparamita 19 @ gmail. com; https: // orcid. org / 0009 - 0009 - 5269 - 3148 +banerjeeparamita19@gmail.com + + + +Author + +Sinha, Shuvra Kanti +0000-0002-2408-7441 +Department of Zoology, Sreegopal Banerjee College, Bagati, Mogra, Hooghly, 712148, West Bengal, India. suvrosinha @ gmail. com; https: // orcid. org / 0000 - 0002 - 2408 - 7441 +suvrosinha@gmail.com + + + +Author + +Mazumdar, Abhijit +0000-0002-2606-9888 +abhijitbu 02 @ gmail. com; https: // orcid. org / 0000 - 0002 - 2606 - 9888 +abhijitbu02@gmail.com + +text + + +Zootaxa + + +2023 + +2023-03-30 + + +5258 + + +4 + + +405 +428 + + + + +http://dx.doi.org/10.11646/zootaxa.5258.4.3 + +journal article +10.11646/zootaxa.5258.4.3 +1175-5326 +7784423 +69D47660-62BF-4E0F-A8D1-B9B27A0051FA + + + + + + + +Culicoides regalis +Majumdar & Das Gupta + + + + + + + +( +Fig 8a–i +) + + + + + + +Culicoides regalis +Majumdar & Das Gupta + +, +in + +Majumdar, Das Gupta & Gangopadhyay 1997: 31 + +; + +Majumdar 1972: 188–192 + +; + +Nandi 2014: 102–104 + + + + + + +Materials examined. +Holotype +( +1 ♀ +), Darjeeling Govt. College, +27.v.1968 +, Coll. Dr. S.K. Das Gupta; + +Allotype +(1 ♁), +Darjeeling Govt. College +, + +21.vi.1968 + +, +Coll. Dr. S.K. Das Gupta +; +13 ♀ +, PHE camp, +Neora Valley National Park +, + +14.iii.2021 + +, +Coll. S.K. Sinha +; 2 ♁ +Bhotaykhadka +, +Neora Valley National Park +, + +19.x.2019 + +, +Coll. S.K. Sinha. + + + + + +Diagnosis. +Antenna with SCo on flagellomeres 1, (9,10), 11–13; mandible with basal 4 broad, outwardly directed teeth; pale spot over r-m cross vein broad, extending to cell m +2 +; broad dark band apical to r-m crossvein continuous to cell m; poststigmatic pale spot separated from vein M +1 +, distal pale spot confluent with vein M +1; +anal cell with constricted distal pale spot. + + +Female. + + +Head +( +Figs 8a and 8b +). Eyes contiguous for 3 facets. Antenna with SCo on flagellomeres 1, (9, 10), 11–13. Third palpal segment long, slender tapering beyond the mid point with numerous capitate sensilla and without sensory pit; fifth segment with 4 apical sensilla. Mandible with basal 4 broad, outwardly directed teeth. + + +Thorax. +Scutum brownish with distinct dark brown anterior and posterior margin; 3 longitudinally dark linear streaks; postscutellum dark. + + +Legs +( +Figs. 8c and 8d +). Brownish; fore and mid femora with pale basal, apical bands, hind femora with pale basal band, fore and mid tibiae with basal pale band, hind tibia with distinct basal and apical bands; hind tibial comb with 6–7 spines, second one long; spur tip frayed; claws equal. + + +Wing +( +Fig. 8e +). Pale area covering wing base, base of veins and proximal half of anal cell extending to posterior wing margin; pale spot over r-m crossvein reaching vein M, continuous to cell m, above Cu fork; poststigmatic pale spot covering almost entire 2 +nd +radial cell and extending broadly to wing margin, sometimes reaching vein M +1 +posteriorly, confluent with proximal pale spots of cells m +1 +and m +2 +; cell r +3 +distal pale spot distant from wing margin, near to vein M +1 +; vein M +1 +bordered by pale streak; cell m +1 +with a distal small oval spot not reaching wing margin; cell m +2 +with two spots, one anterior to Cu fork, the distal one large meeting with wing margin; cell cua +1 +with a pale spot extending to posterior wing margin, touching vein CuA +1 +; proximal portion of dark spot over vein CuA +2 +broad, narrowing posteriorly; anal cell with broad, medially constricted distal pale spot, some with two separated spots. + + +Abdomen +( + +Fig. +8g + +). Brownish with dark streaks; two well developed, ovoid, subequal spermatheca well sclerotized with short oblique necks; tubular rudimentary spermatheca small; small sclerotized ring present. + + +Male. +Similar to female with usual sexual differences. + + +Genitalia +( +Figs. 8h and 8i +). Sternum IX broad with depressed caudal margin. Tergum IX without apicolateral process; posterior margin of tergum IX terminating before apex of gonocoxite. Gonocoxite broad basally, narrowing apically with distinct dorsal root. Gonostylus dilated at base, curved medially, terminating with a blunt tip. Aedeagus weakly sclerotized with short, bent basal arms, stem ending with tubular round tip. Parameres broad basally with basal arms, stem dilated, gradually tapering. + + +Immatures. +Unknown + + +Larval habitat. +Unknown + + + + +Distribution. +India +(Darjeeling, Tindharia, Kurseong, Neora Valley National Park, +West Bengal +) + + + + +Remarks. +This widespread species resembles + +C. isoregalis + +but differs in having a broad pale spot at base of wing extending to posterior wing margin in anal cell and presence of a constricted bilobed distal pale spot in anal cell. This species shows similarity with + +C. neoregalis + +but varies in antennal ratio, palpal ratio ( +Table 1 +), presence of many pale areas in wings, pale spot over cell 2 +nd +radial cell straddling over vein M +1 +, aedeagus terminating in more bulbous tip in + +C. neoregalis + +. + +C. regalis + +looks alike + +C. pararegalis + +have overlapping morphometric data but differs from this in having a larger pale spot in cell r +3 +and a single, constricted distal pale spot in anal cell. These characters may be variable therefore + +C. pararegalis + +so may in fact be a single, variable species but this requires further validation to confirm. +Majumdar (1972) +mentioned variability of SCo on segments +5-8 in + +C. regalis + +and also absent on flagellomeres 9 and +10 in +specimens collected from NVNP. + + + + \ No newline at end of file diff --git a/data/38/0F/A0/380FA045FF91FF96FF1AF4FAFAB395F2.xml b/data/38/0F/A0/380FA045FF91FF96FF1AF4FAFAB395F2.xml new file mode 100644 index 00000000000..03207897a87 --- /dev/null +++ b/data/38/0F/A0/380FA045FF91FF96FF1AF4FAFAB395F2.xml @@ -0,0 +1,264 @@ + + + +A taxonomic revision of the Indian species of the ‘ Aterinervis’ group of Culicoides Latreille Subgenus Hoffmania Fox (Diptera: Ceratopogonidae) + + + +Author + +Sarkar, Ankita +0009-0005-2433-2661 +ankitasarkar 785 @ gmail. com; https: // orcid. org / 0009 - 0005 - 2433 - 2661 +ankitasarkar785@gmail.com + + + +Author + +Banerjee, Paramita +0009-0009-5269-3148 +banerjeeparamita 19 @ gmail. com; https: // orcid. org / 0009 - 0009 - 5269 - 3148 +banerjeeparamita19@gmail.com + + + +Author + +Sinha, Shuvra Kanti +0000-0002-2408-7441 +Department of Zoology, Sreegopal Banerjee College, Bagati, Mogra, Hooghly, 712148, West Bengal, India. suvrosinha @ gmail. com; https: // orcid. org / 0000 - 0002 - 2408 - 7441 +suvrosinha@gmail.com + + + +Author + +Mazumdar, Abhijit +0000-0002-2606-9888 +abhijitbu 02 @ gmail. com; https: // orcid. org / 0000 - 0002 - 2606 - 9888 +abhijitbu02@gmail.com + +text + + +Zootaxa + + +2023 + +2023-03-30 + + +5258 + + +4 + + +405 +428 + + + + +http://dx.doi.org/10.11646/zootaxa.5258.4.3 + +journal article +10.11646/zootaxa.5258.4.3 +1175-5326 +7784423 +69D47660-62BF-4E0F-A8D1-B9B27A0051FA + + + + + + + +Culicoides subregalis +Majumdar & Das Gupta + + + + + + + +( +Fig 9a–i +) + + + + + + +Culicoides subregalis +Majumdar & Das Gupta + +, +in + +Majumdar, Das Gupta & Gangopadhyay 1997: 31 + +; + +Majumdar 1972: 228–232 + +; + +Nandi 2014: 104–106 + + + + + + +FIGURE 9. + +Culicoides subregalis +. + +a) head; b) maxillary palp; c) fore tarsis; d) hind tibial spines; e) halter; f) wing; g) spermathecae with ring; h) male genitalia and i) paramere + + + + +Materials examined. +Holotype +( +1 ♀ +), Darjeeling Govt. College, +23.vi.1968 +, Coll. Dr. S.K. Das Gupta; + +Allotype +(1 ♁), +Darjeeling Govt. College +, + +09.vi.1968 + +, +Coll. Dr. S.K. Das Gupta +; +12 ♀ +, 2 ♁, +Bhotaykhadka +, +Neora Valley National Park +, + +19.x.2019 + +, +Coll. S.K. Sinha. + + + + + +Diagnosis. +Broad dark band apical to r-m crossvein; indistinct pale spot anterior to Cu fork; anal cell with elongate distal pale spot; posterior margin of tergum IX terminating much before apex of gonocoxite. + + +Female. + + +Head +( +Figs. 9a and 9b +). Antenna with SCo on flagellomeres 1, 9–13. Third palpal segment long, slender, tapering past middle bearing capitate sensilla, without sensory pit; fifth segment with 4 apical sensilla. Mandible with basal 4–5 teeth broad. + + +Thorax. +Scutum brown, anterior, posterior portion dark brown; humeral region pale; postscutellum dark brown. + + +Legs +( +Figs 9c and 9d +). Brownish; femora indistinctly pale at bases, fore and mid femora with pale apical bands, tibiae pale at bases; hind tibial comb with 5– 6 spines, second one longest; spur tip frayed; claws equal. + + +Wing +( +Fig. 9f +). Dark area at anal angle; pale spot over r-m crossvein narrow, crossing vein M; poststigmatic pale spot covering half of 2 +nd +radial cell, meeting costa but not reaching vein M +1 +, distal pale spot distinctly distant from apical wing margin; cell m +1 +with an elongate distal pale spot distant from wing margin; cell m +2 +with an indistinct pale spot anterior to Cu fork and distal pale spot broadly meeting wing margin; cell cua +1 +with broad large pale spot extending posteriorly to wing margin; anal cell with a long distal pale spot, perpendicular to and continuous to posterior wing margin. + + +Abdomen +( + +Fig. +9g + +). Brownish with dark tergal streaks; spermatheca two, well developed, pear shaped, subequal, moderately sclerotized with distinct oblique necks; third rudimentary one finger like; small ring present. + + +Male. +Similar to female with usual sexual differences. + + +Genitalia +( +Figs 9h and 9i +). Sternum IX broad with shallow caudomedian excavation. Tergum IX quadrate with round apical margin, a narrow medial cleft, without apicolateral process; posterior margin of tergum IX terminating much before apex of gonocoxite. Gonocoxite broad basally, apex narrow with distinct dorsal root. Gonostylus dilated at base, slightly curved medially, ending in blunt tip. Aedeagus weakly sclerotized with short, bent basal arms. Parameres with sclerotized basal arms with broad base, stem dilated basally, gradually tapering. + + +Immatures. +Unknown + + +Larval habitat. +Unknown + + + + +Distribution. +India +(Darjeeling, Neora Valley National Park, +West Bengal +) + + + + +Remarks. +This species differs from + +C. regalis + +in antennal ratio, width of the pale spot over r-m crossvein, extent of pale area at wing base to anal angle and the long distal pale spot in the anal cell. + +C. subregalis + +is closest to + +C. isoregalis + +and + +C. isoregalis + +seems to be a variant of this species as morphometric data of these two species overlap and but differs in scutal colour, elongated pale spot in cell m +1 +and shape of pale spot in cell cua +1 +that may be resulted due to intraspecific variation but status of these species need to be further strengthened by studying more specimens or by molecular approaches. + + + + \ No newline at end of file diff --git a/data/38/0F/A0/380FA045FF95FF92FF1AF4FAFEFA94AA.xml b/data/38/0F/A0/380FA045FF95FF92FF1AF4FAFEFA94AA.xml new file mode 100644 index 00000000000..9786e6f24e8 --- /dev/null +++ b/data/38/0F/A0/380FA045FF95FF92FF1AF4FAFEFA94AA.xml @@ -0,0 +1,183 @@ + + + +A taxonomic revision of the Indian species of the ‘ Aterinervis’ group of Culicoides Latreille Subgenus Hoffmania Fox (Diptera: Ceratopogonidae) + + + +Author + +Sarkar, Ankita +0009-0005-2433-2661 +ankitasarkar 785 @ gmail. com; https: // orcid. org / 0009 - 0005 - 2433 - 2661 +ankitasarkar785@gmail.com + + + +Author + +Banerjee, Paramita +0009-0009-5269-3148 +banerjeeparamita 19 @ gmail. com; https: // orcid. org / 0009 - 0009 - 5269 - 3148 +banerjeeparamita19@gmail.com + + + +Author + +Sinha, Shuvra Kanti +0000-0002-2408-7441 +Department of Zoology, Sreegopal Banerjee College, Bagati, Mogra, Hooghly, 712148, West Bengal, India. suvrosinha @ gmail. com; https: // orcid. org / 0000 - 0002 - 2408 - 7441 +suvrosinha@gmail.com + + + +Author + +Mazumdar, Abhijit +0000-0002-2606-9888 +abhijitbu 02 @ gmail. com; https: // orcid. org / 0000 - 0002 - 2606 - 9888 +abhijitbu02@gmail.com + +text + + +Zootaxa + + +2023 + +2023-03-30 + + +5258 + + +4 + + +405 +428 + + + + +http://dx.doi.org/10.11646/zootaxa.5258.4.3 + +journal article +10.11646/zootaxa.5258.4.3 +1175-5326 +7784423 +69D47660-62BF-4E0F-A8D1-B9B27A0051FA + + + + + + +Key to the Indian species of +Aterinervis +group + + + + + + + +1. Anal angle of wing entirely pale......................................................................... 2 + + +-. Anal angle of wing with dark marking..................................................................... 4 + + + + + +2. Distal pale spot in cell r 3 reaches wing margin........................................................ + +neoregalis + + + + + +- Distal pale spot in cell r +3 +not reaches wing margin........................................................... 3 + + + + + + +3. Distal pale spot in cell r +3 +large; anal cell with a constricted distal pale spot.................................... + +regalis + + + + + +- Distal pale spot in cell r reduced; anal cell with two separated distal pale spots............................ + +pararegalis + + + + +3 + + + +4. Anal cell with proximal pale spot narrowly constricted medially...................................... + +pseudoregalis + + + + +- Anal cell with proximal pale spot not constricted medially..................................................... 5 + + + + +5. Distal pale spot in cell m 1 reaching wing margin............................................................. 6 + + +- Distal pale spot in cell m + +1 not reaching wing margin................................................. + +quasiregalis + + + + + + + +6. Distal pale spot in cell m +1 +narrow, elongate; posterior margin of tergum IX terminating just before apex of gonocoxite.................................................................................................. + +isoregalis + + + + + +- Distal pale spot in cell m +1 +broad, short; posterior margin of tergum IX terminating much before apex of gonocoxite..................................................................................................... + +subregalis + + + + + + + \ No newline at end of file diff --git a/data/38/0F/C4/380FC484089D5190A4E1372D219B5F75.xml b/data/38/0F/C4/380FC484089D5190A4E1372D219B5F75.xml new file mode 100644 index 00000000000..1742cea85e9 --- /dev/null +++ b/data/38/0F/C4/380FC484089D5190A4E1372D219B5F75.xml @@ -0,0 +1,288 @@ + + + +Review of Afrotropical sceliotracheline parasitoid wasps (Hymenoptera, Platygastridae) + + + +Author + +van Noort, Simon +https://orcid.org/0000-0001-6930-9741 +Research and Exhibitions Department, South African Museum, Iziko Museums of South Africa, PO Box 61, Cape Town, 8000, South Africa & Department of Biological Sciences, University of Cape Town, Private Bag Rondebosch, 7701, Cape Town, South Africa +svannoort@iziko.org.za + + + +Author + +Lahey, Zachary +https://orcid.org/0000-0002-9402-9570 +Department of Evolution, Ecology, and Organismal Biology, The Ohio State University, 1315 Kinnear Road, Columbus, Ohio 43212, USA + + + +Author + +Talamas, Elijah J. +https://orcid.org/0000-0002-1048-6345 +Division of Plant Industry, Florida Department of Agriculture and Consumer Services, Gainesville, FL, USA + + + +Author + +Austin, Andrew D. +Department of Ecology and Evolutionary Biology, School of Biological Sciences, The University of Adelaide, Adelaide 5005, Australia + + + +Author + +Masner, Lubomir +Agriculture and Agri-Food Canada, K. W. Neatby Building, Ottawa, Ontario K 1 A 0 C 6, Canada + + + +Author + +Polaszek, Andrew +https://orcid.org/0000-0002-7171-3353 +Department of Life Sciences, Natural History Museum, Cromwell Road, London SW 7 5 BD, UK + + + +Author + +Johnson, Norman F. +Department of Evolution, Ecology, and Organismal Biology, The Ohio State University, 1315 Kinnear Road, Columbus, Ohio 43212, USA + +text + + +Journal of Hymenoptera Research + + +2021 + +2021-12-23 + + +87 + + +115 +222 + + + + +http://dx.doi.org/10.3897/jhr.87.73770 + +journal article +http://dx.doi.org/10.3897/jhr.87.73770 +1314-2607-87-115 +7137A82A62E34958A48CB05BEA80FE60 +DF6504D9294F5C7F8148AAA6C0D3E01B +5811667 + + + + +Parabaeus nasutus van Noort +sp. nov. + + + + +Figs 25 +, 26 + + + +Material examined. + + + +Holotype + +: +South Africa +• + +; +Northern Cape +, +Swaarweerberg +, +Vredehoek Farm +; + +1613 m + +; +32°26.387'S +, +20°34.501'E +; +29 July-30 September 2010 +; +S. van Noort +; +Yellow pan trap +; +Roggeveld Shale Renosterveld +; SWA09-SUC1-Y05; SAM-HYM-P040757 (SAMC). + + + + +Figure 25. + +Parabaeus nasutus + +van Noort sp. nov. female +holotype +(SAMC) (SAM-HYM-P040757) +A +habitus, lateral view +B +habitus, dorsal view +C +head, mesosoma, lateral view +D +head, mesosoma, dorsal view +E +head, anterior view (inset: data labels) +F +habitus, ventral view. + + + + + +Paratypes + +: +South Africa +• +3♂♂ +, data as for holotype, except for +31 March-29 July 2010 +; SWA09-SUC1-Y04; SAM-HYM-P040756a-c (SAMC) + +. + + + +Figure 26. + +Parabaeus nasutus + +van Noort sp. nov. female +holotype +(SAMC) (SAM-HYM-P040757) +A +head, antenna, ventrolateral view +B +cheek, clypeus, mandibles ventrolateral view +C +toruli, clypeus, mandibles, ventral view +D +mesoscutum, propodeum, dorsal view +E +mesosoma, anterior metasoma, dorso-lateral view +F +scutellum, propodeum, metasoma, dorsal view. + + + + +Excluded from type material. + +South Africa • 1♀; Western Cape, Gamkaberg Nature Reserve; +33°39.941'S +, +21°53.505'E +; 315 m; 19 Feb-30 Mar 2010; S. van Noort; Yellow pan trap; Gamka Thicket; GB09-SUC1-Y28; SAM-HYM-P093813 (SAMC). + + + +Description. + +Female +body length: 0.84 mm. +Colour +of head, metasoma, antennae and fore and mid legs brown; mesosoma and hind legs yellow-brown. + + +Head +as wide as long. Much wider than mesosoma, fractionally narrower than width of metasoma; in dorsal view moderately transverse; clypeus produced into flattened volcano-shaped, nasute-like process with central fovea ringed by a carina; malar sulcus present; frons convexly rounded; occiput vertical, mostly hidden by mesosoma; occipital carina not visible dorsally, not reaching to posterior margins of eyes or lateral ocelli; lateral ocelli connected by hyperoccipital carina forming a sharp dorsal delimitation between occiput and vertex; ocelli forming an obtuse triangle, POL>LOL; in anterior view frons 0.6 +x +width of head; subocular carina absent; gena wide; head covered with coriaceous sculpturing; antennal segments short and robust, clava 2.5 +x +as long as wide. + + + +Mesosoma +. + +Robust, 0.8 +x +width of metasoma, as long as wide; in dorsal view pronotum only visible as narrow strip around anterior margin, pronotal collar with posteriorly orientated, raised, medial bifurcated projection; mesoscutum convexly rounded, posterior margin strongly elevated, with scutellum forming dorsal plateau defined by darker, toothed ellipsoidal carina; posterior face abruptly declivitous; in lateral view pronotal spiracle seen as a small toothed bump at posterodorsal corner of pronotum; tegula absent; mesopleural carina absent; mesopleural carina present; dorsal mesosoma imbricate with associated posteriorly facing setae; pronotum imbricate in dorsal half, smooth with longitudinal striations in ventral half of lateral face; mesopleuron smooth dorsally with longitudinal striations in ventral half; pronotum and mesopleuron fused; metapleuron and dorsolateral propodeum densely covered with fine setae. + + + +Metasoma +. + +In dorsal view oval in shape; anterior margin broad; T1 very narrow, densely setose laterally, base of metasoma without obvious foveate pits (although there are possibly two pits indicated by depressions that are obscured by setae); tergite 1 with bifurcate projecting medial plate; T2 composing virtually all dorsal metasoma; T3-T6 very narrow, strip-like, only seen in posterior view; anterior T2 faintly longitudinally coriaceous, smooth in posterior half, whole surface sparsely setose. + + +Male. +As in females, except for clava, which is more elongate. + + + +Diagnosis. + + +Parabaeus nasutus + +has the following unique morphological apomorphies: elevation of posterior section of mesoscutum and scutellum into a medial projection, which dorsally has a transversely ellipsoidal plateau formed by the scutellum with a 90 degree drop-off posteriorly; base of metasoma without obvious foveolate pits (although there are possibly two pits indicated by depressions that are obscured by setae); T1 with bifurcate projecting medial plate; pronotal collar with posteriorly projecting medial bifurcating raised plate; clypeus produced into dorso-ventrally compressed, volcano-shaped, nasute-like process with a central apical fovea ringed by a carina; occipital carina not visible dorsally. Although + +P. nasutus + +has a number of derived diagnostic characters, from a ground-plan perspective the species is morphologically similar to + +P. peckorum + +sharing the same squamate sculpturing with scattered posteriorly projecting setae on the dorsal mesosoma, and dense setose patches on the metapleuron, dorsolateral propodeum and T1. Colour is, however, different from + +P. peckorum + +, which has a dark brown to black body with lighter brown antennae and legs, and dense white pubescence at the mesosomal-metasomal boundary. + + + +Etymology. +Named for the exceptional clypeal modification into a nasute-like process. Latin adjective. + + +Distribution. +South Africa. + + +Comments. +We suspect that the central fovea ringed by a carina that is terminally situated on the clypeal nasute-like process is olfactory in nature, potentially containing chemo-sensillae that may be involved in host location, although males also possess this adaptation, so possibly it is involved in mate recognition. It is likely that the species lives in the leaf-litter habitat and probably attacks insect or arachnid eggs. + +The single female from Gamkaberg Nature Reserve is uniformly orange-yellow, has a smoother mesopleuron, and weaker clypeal and posterior mesosomal protrusions. Overall, the surface sculpturing is also weaker. The specimen is smaller than the type series specimens and these differences may simply be related to the reduced size. There is, however, the possibility that this specimen represents a second closely related, undescribed species, but until further specimens are acquired to assess the degree of intraspecific variation this specimen is considered to belong to + +P. nasutus + +, but it is excluded from the type material. + + + + \ No newline at end of file diff --git a/data/38/11/45/38114577D6859AC16F248B70998E069A.xml b/data/38/11/45/38114577D6859AC16F248B70998E069A.xml new file mode 100644 index 00000000000..2f8582a0928 --- /dev/null +++ b/data/38/11/45/38114577D6859AC16F248B70998E069A.xml @@ -0,0 +1,126 @@ + + + +A contribution to the study of the Lower Volga center of scarab beetle diversity in Russia: checklist of the tribe Aphodiini (Coleoptera, Scarabaeidae) of Dosang environs + + + +Author + +Frolov, Andrey + + + +Author + +Akhmetova, Lilia + +text + + +Biodiversity Data Journal + + +2013 + +1 + + +979 +979 + + + + +http://dx.doi.org/10.3897/BDJ.1.e979 + +journal article +http://dx.doi.org/10.3897/BDJ.1.e979 +1314-2828-1-979 + + + + +quadriguttatus +Eudolus +Aphodius +Scarabaeidae +Coleoptera +Insecta +Arthropoda +Animalia + + + + +Aphodius quadriguttatus (Herbst, 1783) + + + +Materials + + +Type status: +Other material +Occurrence: recordedBy: +A. V. Frolov, L. A. Akhmetova +; individualCount: +6 +; Location: country: +Russia +; stateProvince: Astrakhan'; locality: +Dosang environs, fixed sands +; decimalLatitude: +46.92 +; decimalLongitude: +47.92 +; Event: samplingProtocol: +cow dung washing +; eventDate: +2007-04-17 +; Record Level: collectionID: urn:lsid:biocol.org:col:34969; institutionCode: +ZIN +; collectionCode: +Coleoptera + + + + +Type status: +Other material +Occurrence: recordedBy: +A. V. Frolov, L. A. Akhmetova +; individualCount: +12 +; Location: country: +Russia +; stateProvince: Astrakhan'; locality: +Dosang environs, fixed sands +; decimalLatitude: +46.92 +; decimalLongitude: +47.92 +; Event: samplingProtocol: +cow dung washing +; eventDate: +2012-05-15 +; Record Level: collectionID: urn:lsid:biocol.org:col:34969; institutionCode: +ZIN +; collectionCode: +Coleoptera + + + + +Ecological interactions + +Feeds on +Cattle and wild herbivore dung. + + + +Distribution +Western Palearctic region from North Africa in the south-west to Altai Mountains the north-east. + + + \ No newline at end of file diff --git a/data/38/11/B1/3811B19C711E6C9D2FB6D2ADCD78499C.xml b/data/38/11/B1/3811B19C711E6C9D2FB6D2ADCD78499C.xml new file mode 100644 index 00000000000..0f6e8eb9c07 --- /dev/null +++ b/data/38/11/B1/3811B19C711E6C9D2FB6D2ADCD78499C.xml @@ -0,0 +1,124 @@ + + + +The Callerya Group redefined and Tribe Wisterieae (Fabaceae) emended based on morphology and data from nuclear and chloroplast DNA sequences + + + +Author + +Compton, James A. + + + +Author + +Schrire, Brian D. + + + +Author + +Koenyves 3, Kalman + + + +Author + +Forest, Felix + + + +Author + +Malakasi, Panagiota + + + +Author + +Sawai Mattapha, + + + +Author + +Sirichamorn, Yotsawate + +text + + +PhytoKeys + + +2019 + +125 + + +1 +112 + + + + +http://dx.doi.org/10.3897/phytokeys.125.34877 + +journal article +http://dx.doi.org/10.3897/phytokeys.125.34877 +1314-2003-125-1 +FFF8910AFFD4A824FFC3AF26FFD1FFD5 +3268023 + + + + +Whitfordiodendron nieuwenhuisii (J.J.Sm.) Dunn, Bull. Misc. Inform. Kew 1912(8): 364 (1912b) + + + + +≡ +Millettia nieuwenhuisii +J.J.Sm., Bull. +Dept +. Agric. Indes +Neerl +. 3: 17 (1906). Type: Indonesia, Kalimantan, [Borneo], Bloe-oe [Bluu river], [cult.] Buitenzorg, Java, 1897-1898, [Anton Willem] Nieuwenhuis 1294 (BO, holo.) + + +≡ +Adinobotrys nieuwenhuisii +(J.J.Sm.) Dunn, Bull. Misc. Inform. Kew 1911(4): 196 (1911) ≡ +Callerya nieuwenhuisii +(J.J.Sm.) Schot, Blumea 39(1-2): 26 (1994) + + += +Adinobotrys myrianthus +Dunn, Bull. Misc. Inform. Kew 1911(4): 196 (1911). Type: "Sarawak, 1865 +-1868" +, [Odoardo] Beccari 875, K000881001 (K, lecto.! designated here); S08-15160 (S, isolecto.); P03659572 (P, isolecto.!); M-0233444 (M, isolecto.!) ≡ +Whitfordiodendron myrianthum +(Dunn) Dunn, Bull. Misc. Inform. Kew 1912(8): 364 (1912). + + += +Millettia cuspidata +Ridl., Bull. Misc. Inform. Kew 1929(8): 254 (1929). Type: "Sarawak, Matang woods, flowers pinkish", January 1915, [Henry Nicholas] Ridleys.n.., K000880995 (K, holo.!). + + + +Illustration. +http://www.asianplant.net/Fabaceae/Callerya_nieuwenhuisii.htm + + +Distribution. +Brunei; Indonesia (Borneo: Kalimantan); Malaysia (Borneo: Sarawak, Sabah). + + +Habitat. +Climbing near rivers or on steep slopes in evergreen forest from sea level to 1300 m. + + + \ No newline at end of file diff --git a/data/38/11/C3/3811C3F77FC3589DBDB7CC109DA7BE5C.xml b/data/38/11/C3/3811C3F77FC3589DBDB7CC109DA7BE5C.xml new file mode 100644 index 00000000000..c0ad5e062ce --- /dev/null +++ b/data/38/11/C3/3811C3F77FC3589DBDB7CC109DA7BE5C.xml @@ -0,0 +1,115 @@ + + + +Catalogue of Geadephaga (Coleoptera, Adephaga) of America, north of Mexico + + + +Author + +Bousquet, Yves +Agriculture and Agri-Food Canada, Central Experimental Farm, Ottawa, Ontario, Canada +bousquety1@yahoo.com + +text + + +ZooKeys + + +2012 + +2012-11-28 + + +245 + + +1 +1722 + + + + +http://dx.doi.org/10.3897/zookeys.245.3416 + +journal article +http://dx.doi.org/10.3897/zookeys.245.3416 +1313-2970-245-1 +FFFF52503A0AFF882450FFB66D45FF8E +578462 + + + + +Subgenus +Anomoglossus Chaudoir, 1857 + + + + +Anomoglossus +Chaudoir, 1857: 4. Type species: + +Chlaenius emarginatus + +Say, 1823 designated by Bell (1960: 105). Etymology (original). From the Greek +anomos +(a +bnormal +) and +glossa +(tongue), alluding to the unusual shape of the ligula (" +ligula omnino abnormis +"), corresponding to the glossa and paraglossae or the glossal sclerite, of the adult [masculine]. + + + +Diversity. +Three species in eastern North America. + + +Taxonomic Note. + +The generic name + +Agreuter + +Lepeletier and Audinet-Serville (in Latreille et al. 1828: 633) was proposed for two species, + +Chlaenius chlorodius + +Dejean, 1826 and + +Chlaenius elegantulus + +Dejean, 1826 (= + +Chlaenius pusillus + +Say, 1823). Bousquet (2002b: 6) designated + +Chlaenius elegantulus + +as type species and so the name is listed as a synonym of + +Anomoglossus + +Chaudoir (e.g., Lorenz 2005: 333). However, Duponchel (1840a: 196) had selected + +Chlaenius chlorodius + +as the type species and so + +Agreuter + +is a senior synonym of + +Amblygenius + +LaFerte-Senectere +, 1851. + + + + \ No newline at end of file diff --git a/data/38/11/D4/3811D4A8A5304C66F177F3FDCCE36CA7.xml b/data/38/11/D4/3811D4A8A5304C66F177F3FDCCE36CA7.xml new file mode 100644 index 00000000000..313544d5f58 --- /dev/null +++ b/data/38/11/D4/3811D4A8A5304C66F177F3FDCCE36CA7.xml @@ -0,0 +1,79 @@ + + + +Cyanobacteria of Greece: an annotated checklist + + + +Author + +Gkelis, Spyros + + + +Author + +Ourailidis, Iordanis + + + +Author + +Panou, Manthos + + + +Author + +Pappas, Nikos + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +10084 +10084 + + + + +http://dx.doi.org/10.3897/BDJ.4.e10084 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e10084 +1314-2828-4-10084 + + + + + +Komvophoron pallidum (Skuja) Anagnostidis & +Komarek +, 1988 + + + + + +Pseudanabaena pallida + + + +Notes + + +Anagnostidis and +Economou-Amilli +1980 + + + + + \ No newline at end of file diff --git a/data/38/11/E6/3811E6C9D2EE4C3D74A511DF9213EC55.xml b/data/38/11/E6/3811E6C9D2EE4C3D74A511DF9213EC55.xml new file mode 100644 index 00000000000..c6ebd4fd7e1 --- /dev/null +++ b/data/38/11/E6/3811E6C9D2EE4C3D74A511DF9213EC55.xml @@ -0,0 +1,112 @@ + + + +Faunistic diversity of spiders (Araneae) in Galichitsa mountain (FYR Macedonia) + + + +Author + +Deltshev, Christo + + + +Author + +Komnenov, Marjan + + + +Author + +Blagoev, Gergin + + + +Author + +Georgiev, Teodor + + + +Author + +Lazarov, Stoyan + + + +Author + +Stojkoska, Emilija + + + +Author + +Naumova, Maria + +text + + +Biodiversity Data Journal + + +2013 + +1 + + +977 +977 + + + + +http://dx.doi.org/10.3897/BDJ.1.e977 + +journal article +http://dx.doi.org/10.3897/BDJ.1.e977 +1314-2828--977 + + + + +viaria +Microneta +Araneae +Arachnida +Arthropoda +Animalia + + + + +Microneta viaria (Blackwall, 1841) + + + +Materials +Type status: Other material + +Occurrence: recordedBy: +C. Deltshev & G. Blagoev +; sex: +1 male +; Location: country: +FYR of Macedonia +; locality: +Galichitsa Mt., Resen +; verbatimElevation: +1000 m +; Event: eventDate: + +30-08-2002 + + + + +Distribution +Holarctic. + + + \ No newline at end of file diff --git a/data/38/12/B0/3812B039BC75FFF2CEBFFB93FE57709D.xml b/data/38/12/B0/3812B039BC75FFF2CEBFFB93FE57709D.xml new file mode 100644 index 00000000000..904d27b55c9 --- /dev/null +++ b/data/38/12/B0/3812B039BC75FFF2CEBFFB93FE57709D.xml @@ -0,0 +1,201 @@ + + + +Neohormodochis septispora gen. et sp. nov. (Stictidaceae) from Yunnan Province, China + + + +Author + +Wei, De-Ping +Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai, 50200, Thailand & CAS Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, P. R. China + + + +Author + +Gentekaki, Eleni +Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand & School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand + + + +Author + +Wanasinghe, Dhanushka N. +CAS Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, P. R. China & Centre for Mountain Futures, Kunming Institute of Botany, Chinese Academy of Sciences, Honghe County 654400, Yunnan, P. R. China Innovative Institute of Plant Health, Zhongkai University of Agriculture and Engineering, Haizhu District, Guangzhou 510225, P. R. China + + + +Author + +Hyde, Kevin D. +CAS Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, P. R. China & Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand + + + +Author + +To-Anun, Chaiwat +0000-0001-8098-3390 +Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai, 50200, Thailand & chaiwat. toanun @ gmail. com; https: // orcid. org / 0000 - 0001 - 8098 - 3390 +chaiwat.toanun@gmail.com + + + +Author + +Cheewangkoon, Ratchadawan +0000-0001-8576-3696 +Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai, 50200, Thailand & ratchadawan. c @ cmu. ac. th; https: // orcid. org / 0000 - 0001 - 8576 - 3696 +ratchadawan.c@cmu.ac.th + +text + + +Phytotaxa + + +2022 + +2022-11-23 + + +573 + + +2 + + +247 +261 + + + + +http://dx.doi.org/10.11646/phytotaxa.573.2.5 + +journal article +194616 +10.11646/phytotaxa.573.2.5 +80c0dfdc-2eb9-4d4d-b10d-b7cb911acc21 +1179-3163 +7349970 + + + + + + +Neohormodochis +D.P.Wei & K.D.Hyde + +, + +gen. nov. + + + + + +Index Fungorum number: IF559771 +Faces of Fungi number: FoF12297 + + + +Etymology: The epithet refers to the close phylogenetic relationship with + +Hormodochis + +. + + + + +Type +species: + +Neohormodochis septispora +D. P. Wei and K. D. Hyde + +, + +sp. nov. + + + + + +Saprobic on dead twigs. +Sexual morph +: Undetermined. +Asexual morph +: +Conidiomata +perithecial, immersed, conical to subglobose, gregarious, white-pruinose. +Conidiomatal wall +consisting of hyaline, intricate hyphae, encompassed with crystalline substances. +Conidiophores +reduced to conidiogenous cells. +Conidiogenous cells +holoblastic, hyaline, cylindrical, developing from hyphae of conidiomatal wall. +Conidia +hyaline, ellipsoidal, twocelled, occasionaly asepate, slightly curved, forming branched chains. + + + + +Notes: + +Neohormodochis + +was introduced to accommodate the new species + +N. septispora + +which was found on dead twigs in +Yunnan Province +, +China +. The new species nested with + +Hormodochis + +as a sister clade. + +Hormodochis + +is known from three asexual morphic species viz. + +H. aggregata +, +H. eucalypti + +and + +H. melanochlora + +. All three species have non-pruinose conidiomata, non-crystalline conidiomatal wall of thin-walled, brown +textura angularis +, holothallic conidiogenous cells with upper cells becoming fertile, septate and disarticulating into arthroconidia. The arthroconidia are olivaceous brown, aseptate, subcylindrical to somewhat doliiform, with truncate ends ( + +Crous +et al. +2020a + +). However, + +Neohormodochis septispora + +produces white-pruinose conidiomata, crystalline conidiomatal wall and hyaline, holobalstic conidiogenous cells with upper cells becoming fertile and budding new conidia rather than arthroconidia. The conidia of + +N. septispora + +are hyaline, ellipsoidal, dominantly septate, slightly curved, round at both ends. Phylogenetic placement and differences on morphology of conidiomata, conidiomatal wall, and conidia as well as conidiogenesis separate our collections from + +Hormodochis +. + + + + + \ No newline at end of file diff --git a/data/38/12/B0/3812B039BC77FFFFCEBFFF79F9CB74CF.xml b/data/38/12/B0/3812B039BC77FFFFCEBFFF79F9CB74CF.xml new file mode 100644 index 00000000000..931bafbb4b3 --- /dev/null +++ b/data/38/12/B0/3812B039BC77FFFFCEBFFF79F9CB74CF.xml @@ -0,0 +1,347 @@ + + + +Neohormodochis septispora gen. et sp. nov. (Stictidaceae) from Yunnan Province, China + + + +Author + +Wei, De-Ping +Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai, 50200, Thailand & CAS Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, P. R. China + + + +Author + +Gentekaki, Eleni +Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand & School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand + + + +Author + +Wanasinghe, Dhanushka N. +CAS Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, P. R. China & Centre for Mountain Futures, Kunming Institute of Botany, Chinese Academy of Sciences, Honghe County 654400, Yunnan, P. R. China Innovative Institute of Plant Health, Zhongkai University of Agriculture and Engineering, Haizhu District, Guangzhou 510225, P. R. China + + + +Author + +Hyde, Kevin D. +CAS Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, P. R. China & Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand + + + +Author + +To-Anun, Chaiwat +0000-0001-8098-3390 +Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai, 50200, Thailand & chaiwat. toanun @ gmail. com; https: // orcid. org / 0000 - 0001 - 8098 - 3390 +chaiwat.toanun@gmail.com + + + +Author + +Cheewangkoon, Ratchadawan +0000-0001-8576-3696 +Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai, 50200, Thailand & ratchadawan. c @ cmu. ac. th; https: // orcid. org / 0000 - 0001 - 8576 - 3696 +ratchadawan.c@cmu.ac.th + +text + + +Phytotaxa + + +2022 + +2022-11-23 + + +573 + + +2 + + +247 +261 + + + + +http://dx.doi.org/10.11646/phytotaxa.573.2.5 + +journal article +194616 +10.11646/phytotaxa.573.2.5 +80c0dfdc-2eb9-4d4d-b10d-b7cb911acc21 +1179-3163 +7349970 + + + + + + +Neohormodochis septispora +D. P. Wei & K. D. Hyde + +, + +sp. nov. + +( +Figure 2 +) + + + + +Index Fungorum number: IF 559772 +Faces of Fungi number: FoF12298 + + + +FIGURE 2. + +Neohormodochis septispora + +(HKAS 124171, holotype). +a +Substrate. +b, c +Conidiomata. +d, e +Vertical section through conidiomata. +f +Crystals. +g +Conidiomatal wall. +h, i +Conidiogenous cells bearing conidia. +j, k +Conidial chains. +l, m +Developing conidia. +n, o +Conidia. +p +Germinal conidium. +q, r +Upper and lower view of cultures. Scar bar: d, e = 150 um, f, g, j, p = 30 um, h, i, k, n, o = 10 um, l, m = 5 um. + + + + +Etymology: The epithet “ + +septispora + +” refers to the septate conidia. + + + + + +Holotype +: +China +, +Yunnan Province +, +Kunming +, +Panlong district +, +Kunming Institute of Botany +, on an unidentified dead twig, + +31 March 2021 + +, Cuijinyi Li, +KLCJY54 +( +HKAS 124171 +, + +holotype + +), ( +KUNCC 22-10806 +, ex-type culture). + + + + + +Saprobic on an unidentified dead twigs. +Sexual morph +: Undetermined. +Asexual morph +: +Conidiomata +165–360 × 140–340 (x̄ = 282 × 252, n = 10) μm, perithecial, immersed, conical to subglobose, white-pruinose, gregarious, with olivaceous green content. +Conidiomatal wall +11–30 (x̄ = 19, n = 30) μm, consisting of hyaline, intricate hyphae, being encompassed by a layer of irregularly-shaped crystals. +Conidiophores +reduced to conidiogenous cells. +Conidiogenous cell +3.5–10 × 0.8–2.4 (x̄ = 7 × 1.6, n = 25) μm, arising from stromatic cells, hyaline, cylindrical, thin-walled, the first conidium becoming conidiogenous by apical wall-building to +form connected +chain. +Conidia +7.6–12 × 2–3.8 (x̄ = 9.5 × 3.3, n = 40) μm, hyaline, ellipsoidal, two-celled, occasionally asepate, slightly curved, arranged in branched chain. + + + + +Culture characteristics: isolates were obtained from germinating conidia. Colony slow-growing, reaching +2 cm +after 8 weeks on PDA, white, circular, mycelia dense, velvety, reverse creamy-yellow. + + + + +Additional materials examined: + +China +, +Yunnan Province +, +Kunming +, +Panlong district +, +Heilongtan Park +, + +31 March 2021 + +, +Cuijinyi Li + +, + +HLCJY57 +( +HKAS 124172 +), ( +KUNCC22-10807 +, living culture) + +; + +HLCJY58 +( +HKAS 124174 +), ( +KUNCC22-10808 +, living culture) + +; + +HLCJY59 +( +HKAS 124173 +), ( +KUNCC22-10809 +, living culture); +ibid +. +Songhuaba +reservoir, + +11 December 2021 + +, +De-Ping Wei + +, + +SHB1225 +( +HKAS 124170 +), ( +KUNCC22-10810 +, living culture) + +. + + + + +Notes: Phylogenetically, + +Neohormodochis septispora + +has a sister affiliation to a clade comprising + +Hormodochis aggregata + +, + +H. melanochlora + +and + +H. eucalypti + +( +Figure 1 +). Morphologically, + +N. septispora + +is similar with + +H. aggregata + +by catenulate conidia but differs by the hyaline, ellipsodial and septate conidia while it is olivaceous brown, subcylindrical to doliiform, and aseptate in the latter ( + +Crous +et al. +2020a + +). + +Hormodochis melanochlora + +is distinct by erumpent, globose, brown conidiomata that are immersed, conical to globose, white-pruinose from + +N. septispora +( + +Crous +et al. +2020a + +) + +. + +Hormodochis eucalypti + +(syn. + +Phacidiella eucalypt + +) has dark brown to black conidiomata and subcylindrical to barrel-shaped conidia that are dramatically different from + +N. septispora + +( + +Crous +et al. +2007 + +, +2020b +). + + + + \ No newline at end of file diff --git a/data/38/12/BB/3812BB8F4F05A42279BD22229EBD8673.xml b/data/38/12/BB/3812BB8F4F05A42279BD22229EBD8673.xml new file mode 100644 index 00000000000..4b9ea2792d1 --- /dev/null +++ b/data/38/12/BB/3812BB8F4F05A42279BD22229EBD8673.xml @@ -0,0 +1,281 @@ + + + +Annelids of the eastern Australian abyss collected by the 2017 RV ' Investigator' voyage + + + +Author + +Gunton, Laetitia M. +Australian Museum Research Institute, Sydney, Australia +laetitia.gunton@austmus.gov.au + + + +Author + +Kupriyanova, Elena K. +Australian Museum Research Institute, Sydney, Australia & Macquarie University, Sydney, Australia + + + +Author + +Alvestad, Tom +Department of Natural History, University Museum of Bergen, University of Bergen, Bergen, Norway + + + +Author + +Avery, Lynda +Museums Victoria, Melbourne, Australia + + + +Author + +Blake, James A. +https://orcid.org/0000-0001-8217-9769 +Aquatic Research & Consulting, Duxbury, Massachusetts, USA + + + +Author + +Biriukova, Olga +Museum and Art Gallery of the Northern Territory, Darwin, Australia + + + +Author + +Boeggemann, Markus +University of Vechta, Vechta, Germany + + + +Author + +Borisova, Polina +P. P. Shirshov Institute of Oceanology, Russian Academy of Sciences, Moscow, Russia + + + +Author + +Budaeva, Nataliya +Department of Natural History, University Museum of Bergen, University of Bergen, Bergen, Norway & P. P. Shirshov Institute of Oceanology, Russian Academy of Sciences, Moscow, Russia + + + +Author + +Burghardt, Ingo +Australian Museum Research Institute, Sydney, Australia + + + +Author + +Capa, Maria +https://orcid.org/0000-0002-5063-7961 +Department of Biology, University of the Balearic Islands, Palma, Spain + + + +Author + +Georgieva, Magdalena N. +Natural History Museum, London, UK + + + +Author + +Glasby, Christopher J. +https://orcid.org/0000-0002-9464-1938 +Museum and Art Gallery of the Northern Territory, Darwin, Australia + + + +Author + +Hsueh, Pan-Wen +Department of Life Sciences, National Chung Hsing University, Taichung City, China + + + +Author + +Hutchings, Pat +Australian Museum Research Institute, Sydney, Australia & Macquarie University, Sydney, Australia + + + +Author + +Jimi, Naoto +https://orcid.org/0000-0001-8586-3320 +National Institute of Polar Research, Tachikawa, Tokyo, Japan + + + +Author + +Kongsrud, Jon A. +Department of Natural History, University Museum of Bergen, University of Bergen, Bergen, Norway + + + +Author + +Langeneck, Joachim +https://orcid.org/0000-0003-3665-8683 +Department of Biology, University of Pisa, Pisa, Italy + + + +Author + +Meissner, Karin +Forschungsinstitut Senckenberg, DZMB, Hamburg, Germany + + + +Author + +Murray, Anna +https://orcid.org/0000-0002-1765-1286 +Australian Museum Research Institute, Sydney, Australia + + + +Author + +Nikolic, Mark +Museums Victoria, Melbourne, Australia + + + +Author + +Paxton, Hannelore +https://orcid.org/0000-0001-7086-5219 +Australian Museum Research Institute, Sydney, Australia & Macquarie University, Sydney, Australia + + + +Author + +Ramos, Dino +https://orcid.org/0000-0002-4069-5383 +Natural History Museum, London, UK + + + +Author + +Schulze, Anja +Texas A & M University at Galveston, Galveston, TX, USA + + + +Author + +Sobczyk, Robert +Department of Zoology of Invertebrates and Hydrobiology, University of Lodz, Lodz, Poland + + + +Author + +Watson, Charlotte +Museum and Art Gallery of the Northern Territory, Darwin, Australia + + + +Author + +Wiklund, Helena +Natural History Museum, London, UK & Gothenburg Global Biodiversity Centre and University of Gothenburg, Gothenburg, Sweden + + + +Author + +Wilson, Robin S. +https://orcid.org/0000-0002-9441-2131 +Museums Victoria, Melbourne, Australia + + + +Author + +Zhadan, Anna +Biological Faculty, Lomonosov Moscow State University, Moscow, Russia + + + +Author + +Zhang, Jinghuai +South China Sea Environmental Monitoring Centre, State Oceanic Administration, Guangzhou, China + +text + + +ZooKeys + + +2021 + +2021-02-24 + + +1020 + + +1 +198 + + + + +http://dx.doi.org/10.3897/zookeys.1020.57921 + +journal article +http://dx.doi.org/10.3897/zookeys.1020.57921 +1313-2970-1020-1 +CC23B8CE8C8E473CBD8C44E74252A33D +F6561609F0F15EE8907C94528CA44E4F + + + + +Ophelina sp. + + + +Diagnosis. + +Following synonymy of + +Ammotrypanella + +and + +Ophelina + +( +Blake and Maciolek 2019a +). Bluntly conical prostomium with oval palpode having an enlarged base. 32 chaetigers. Chaetiger 24-32 ventrally located and compressed. Chaetigers 1-6 shorter than midbody chaetigers, having more abundant chaetae. Branchial scars present from chaetigers 24-30. Anal funnel damaged, slightly longer than the last two posterior chaetigers, directed dorsally. + + + +Records. +15 specimens. Suppl. material 1: ops. 9, 16, 27, 31, 33, 55, 79, 96 (AM). 46 specimens. Suppl. material 1: ops. 9, 16, 31, 33, 45, 54, 76, 79, 98, 110, 134 (NHMUK). + + + \ No newline at end of file diff --git a/data/38/13/92/381392C1A9607F4D9E2659B265D302F3.xml b/data/38/13/92/381392C1A9607F4D9E2659B265D302F3.xml new file mode 100644 index 00000000000..00b945e18be --- /dev/null +++ b/data/38/13/92/381392C1A9607F4D9E2659B265D302F3.xml @@ -0,0 +1,104 @@ + + + +Catalogue of Geadephaga (Coleoptera, Adephaga) of America, north of Mexico + + + +Author + +Bousquet, Yves +Agriculture and Agri-Food Canada, Central Experimental Farm, Ottawa, Ontario, Canada +bousquety1@yahoo.com + +text + + +ZooKeys + + +2012 + +2012-11-28 + + +245 + + +1 +1722 + + + + +http://dx.doi.org/10.3897/zookeys.245.3416 + +journal article +http://dx.doi.org/10.3897/zookeys.245.3416 +1313-2970-245-1 +FFFF52503A0AFF882450FFB66D45FF8E +578462 + + + + +Stenolophus incultus Casey, 1914 + + + + +Stenolophus incultus +Casey, 1914: 275. Type locality: "Truckee [Nevada County], California" (original citation). Lectotype (♀), designated by Lindroth (1975: 143), in USNM [# 48040]. + + +Stenolophus abstinens +Casey, 1914: 273. Type locality: +"Arizona" +(original citation). Two syntypes in USNM [# 48037]. +New synonymy +(Gerald R. Noonan pers. comm. 2008). + + +Stenolophus remissus +Casey, 1914: 274. Type locality: "southern California" (original citation). One syntype in USNM [# 48038]. +New synonymy +(Gerald R. Noonan pers. comm. 2008). + + +Stenolophus consors +Casey, 1914: 276. Type locality: "Gualala River, Mendocino Co[unty], California" (original citation). Lectotype (♂), designated by Lindroth (1975: 143), in USNM [# 48041]. Synonymy established by Lindroth (1968: 911). + + +Stenolophus debiliceps +Casey, 1914: 276. Type locality: "Lake Tahoe [Placer County], California" (original citation). Holotype [by monotypy] (♀) in USNM [# 48042]. Synonymy established by Lindroth (1968: 911). + + + +Distribution. + +This species is found from Vancouver Island (Lindroth 1968: 911) to northern Idaho (Hatch 1953: 183), south to +"Arizona" +(Casey 1914: 273, as + +Stenolophus abstinens + +) and southern California (Casey 1914: 274, as + +Stenolophus remissus + +). The record from +"Montana" +(Bousquet and Larochelle 1993: 220) needs confirmation. + + + +Records. + +CAN +: BC (VCI) +USA +: AZ, CA, ID, OR, UT, WA [MT] + + + + \ No newline at end of file diff --git a/data/38/14/54/381454132EE0F9F14B32AE16F2023DD2.xml b/data/38/14/54/381454132EE0F9F14B32AE16F2023DD2.xml new file mode 100644 index 00000000000..b4ef6b80e7f --- /dev/null +++ b/data/38/14/54/381454132EE0F9F14B32AE16F2023DD2.xml @@ -0,0 +1,75 @@ + + + +A biodiversity hotspot for Microgastrinae (Hymenoptera, Braconidae) in North America: annotated species checklist for Ottawa, Canada + + + +Author + +Fernandez-Triana, Jose + + + +Author + +Boudreault, Caroline + + + +Author + +Buffam, Joel + + + +Author + +Mclean, Ronald + +text + + +ZooKeys + + +2016 + +633 + + +1 +93 + + + + +http://dx.doi.org/10.3897/zookeys.63.10480 + +journal article +http://dx.doi.org/10.3897/zookeys.63.10480 +1313-2970-633-1 +DEFC153072414BA6B778CA63DB45B422 + + + + +Taxon +classification Animalia Hymenoptera Braconidae + + + + +Microplitis kewleyi Muesebeck, 1922 + + + +Distribution. +NEA. + + +Material examined. +Ontario, Ottawa, city garden, 45.3561 -75.7069, 10-13.x.2008, H. Goulet, Voucher Code: WMIC0210; 10.viii-1.ix.2007, H. Goulet, Voucher Code: WMIC0204, WMIC0205, WMIC0206, WMIC0215, WMIC0217, WMIC0220; 20-29.ix.2008, H. Goulet, Voucher Code: WMIC0211; 30.vii-10.viii.2007, H. Goulet, Voucher Code: WMIC0196; Voucher Code: WMIC0208; 45.3561 -75.707, 10.viii.2007, H. Goulet, Voucher Code: CAM0169; 19.ix.2007, H. Goulet, Voucher Code: CAM0195. + + + \ No newline at end of file diff --git a/data/38/14/82/381482DD5546F9BAD5DE5F658F341C59.xml b/data/38/14/82/381482DD5546F9BAD5DE5F658F341C59.xml new file mode 100644 index 00000000000..9ad82bea76c --- /dev/null +++ b/data/38/14/82/381482DD5546F9BAD5DE5F658F341C59.xml @@ -0,0 +1,98 @@ + + + +Order Rodentia - Family Caviidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 2 + + + +1552 +1556 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316535 + + + + + +Galea musteloides +subsp. +musteloides +Meyen 1832 + + + + + + + +Galea musteloides +subsp. +musteloides +Meyen 1832 + +, +Nova. Acta Acad. Caes. Leop.-Carol., 16: 597 + +. + + + + +Type Locality: + +Peru +, Paso de +Tacna +, on road to Lake Titicaca. + + + + + +Synonyms: + +Galea musteloides +subsp. +boliviensis +(Waterhoues 1848) + +; + +Galea musteloides +subsp. +comes +Thomas 1919 + +. + + + + \ No newline at end of file diff --git a/data/38/14/A7/3814A7C60344010DC8EDDB5827B1148B.xml b/data/38/14/A7/3814A7C60344010DC8EDDB5827B1148B.xml new file mode 100644 index 00000000000..8b20d385bdb --- /dev/null +++ b/data/38/14/A7/3814A7C60344010DC8EDDB5827B1148B.xml @@ -0,0 +1,54 @@ + + + +Species plantarum: exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas + + + +Author + +Linnaeus, Carolus + +text + +1753 +Laurentius Salvius + +Stockholm + + + +https://doi.org/10.5962/bhl.title.669 + +book +10.5281/zenodo.3931989 +3931989 + + + + +Ipomoea glaucifolia +, +spec. nov. + + + +11. Ipomoea foliis sagittatis postice truncatis, pedunculis bifloris. + +Convolvulus foliis cordato-lanceolatis. +Hort. cliff.67. + + +Convolvulus stellatus arvensis, folio glauco. +Dill. elth. 103. t.87. f.101. + + + + +Habitat in +Mexicae +arvis. + + + + \ No newline at end of file diff --git a/data/38/14/FE/3814FE63F30067C04C3637081914FAC0.xml b/data/38/14/FE/3814FE63F30067C04C3637081914FAC0.xml new file mode 100644 index 00000000000..7e083ecbf3d --- /dev/null +++ b/data/38/14/FE/3814FE63F30067C04C3637081914FAC0.xml @@ -0,0 +1,70 @@ + + + +Catalogue of Geadephaga (Coleoptera, Adephaga) of America, north of Mexico + + + +Author + +Bousquet, Yves +Agriculture and Agri-Food Canada, Central Experimental Farm, Ottawa, Ontario, Canada +bousquety1@yahoo.com + +text + + +ZooKeys + + +2012 + +2012-11-28 + + +245 + + +1 +1722 + + + + +http://dx.doi.org/10.3897/zookeys.245.3416 + +journal article +http://dx.doi.org/10.3897/zookeys.245.3416 +1313-2970-245-1 +FFFF52503A0AFF882450FFB66D45FF8E +578462 + + + + +Loxandrus sculptilis Bates, 1884 + + + + +Loxandrus sculptilis +Bates, 1884: 278. Type locality: +"Tole +[ +Chiriqui +], Panama" (original citation for the lectotype). Lectotype (♂), designated by Allen (1972: 38), in BMNH. + + + +Distribution. +This species ranges from southern Texas (Allen and Ball 1980: 501) and central Sinaloa south to Panama [see Allen 1972: Fig. 153]. + + +Records. + +USA +: TX - Mexico, Panama + + + + \ No newline at end of file diff --git a/data/38/15/12/3815123A657F356122680D2C15BFBA1B.xml b/data/38/15/12/3815123A657F356122680D2C15BFBA1B.xml new file mode 100644 index 00000000000..57049cc89b8 --- /dev/null +++ b/data/38/15/12/3815123A657F356122680D2C15BFBA1B.xml @@ -0,0 +1,62 @@ + + + +Genera of the Asian Catfish Families Sisoridae and Erethistidae (Teleostei: Siluriformes). + + + +Author + +Alfred W. Thomson + + + +Author + +Lawrence M. Page + +text + + +Zootaxa + + +2006 + +1345 + + +1 +96 + + + + +http://www.zoobank.org/urn:lsid:zoobank.org:pub:25EFA792-7DA4-4E0D-A69A-12591B8422DE + +journal article +z01345p001 +25EFA792-7DA4-4E0D-A69A-12591B8422DE + + + + +Glyptothorax conirostre +: + + + + + +Ganges drainage +: + +SU +61433 + +(3; 75.7-91.4). + + + + + \ No newline at end of file diff --git a/data/38/15/79/38157904798C57F6AFC239429BB4F61D.xml b/data/38/15/79/38157904798C57F6AFC239429BB4F61D.xml new file mode 100644 index 00000000000..7bbc42cba8c --- /dev/null +++ b/data/38/15/79/38157904798C57F6AFC239429BB4F61D.xml @@ -0,0 +1,75 @@ + + + +A checklist of vascular plants of the W National Park in Burkina Faso, including the adjacent hunting zones of Tapoa-Djerma and Kondio + + + +Author + +Nacoulma, Blandine M. I. +Universite Joseph Ki-Zerbo, Ouagadougou, Burkina Faso + + + +Author + +Schmidt, Marco +Senckenberg Biodiversity and Climate Research Centre, Frankfurt am Main, Germany & Palmengarten, Frankfurt am Main, Germany +https://orcid.org/0000-0001-6087-6117 +mschmidt@senckenberg.de + + + +Author + +Hahn, Karen +Goethe University, Frankfurt am Main, Germany + + + +Author + +Thiombiano, Adjima +Universite Joseph Ki-Zerbo, Ouagadougou, Burkina Faso + +text + + +Biodiversity Data Journal + + +2020 + +8 + + +54205 +54205 + + + + +http://dx.doi.org/10.3897/BDJ.8.e54205 + +journal article +http://dx.doi.org/10.3897/BDJ.8.e54205 +1314-2828-8-e54205 +AC04300B71A5532C90F2702393102067 + + + + +Euphorbia hirta L. + + + +Distribution +Pantropical + + +Notes +Life Form: therophyte + + + \ No newline at end of file diff --git a/data/38/16/94/381694C5B0D8066E81ED9A1A46A9A780.xml b/data/38/16/94/381694C5B0D8066E81ED9A1A46A9A780.xml new file mode 100644 index 00000000000..0d3c99c5a65 --- /dev/null +++ b/data/38/16/94/381694C5B0D8066E81ED9A1A46A9A780.xml @@ -0,0 +1,48 @@ + + + +Glanures myrmecologiques en 1922. + + + +Author + +Forel, A. + +text + + +Revue Suisse de Zoologie + + +1922 + +30 + + +87 +102 + + + + +http://antbase.org/ants/publications/4075/4075.pdf + +journal article +4075 + + + + +Neoponera apicalis Latr. v. verenae +n. v. + + + +Longueur: 10 mm. Plus longue que le type de l'espece. Les scapes depassent l'occiput de pres d'un quart de leur longueur (de plus d'un cinquieme chez le type). Articles du funicule aussi un peu plus longs. Les cotes de la tete sont notablement plus convexes, ce qui rend la tete plus large au milieu. La face declive de l'epinotum est plus nettement separee de la face basale, sans etre clairement bordee. La base du petiole est plus longue, egale a sa hauteur (plus courte chez le type). Du reste identique. + + +Panama (Christophersen). + + + \ No newline at end of file diff --git a/data/38/16/B2/3816B2B00988539FA408D8FE85619093.xml b/data/38/16/B2/3816B2B00988539FA408D8FE85619093.xml new file mode 100644 index 00000000000..7f3bc092f2d --- /dev/null +++ b/data/38/16/B2/3816B2B00988539FA408D8FE85619093.xml @@ -0,0 +1,198 @@ + + + +Checklist of the suborder Terebrantia (Thysanoptera): generic diversity and species composition in Xishuangbanna, Yunnan Province, China + + + +Author + +Elie, Ntirenganya +https://orcid.org/0000-0002-4603-5693 +Plant Protection College, Yunnan Agricultural University, Kunming, 650201, China & Rwandan Association of Ecologists (ARECO Rwanda), Kigali, Rwanda +elientirenganya@gmail.com + + + +Author + +Yajin, Li +Agronomy and Biotechnology College, Yunnan Agricultural University, Kunming, 650201, China + + + +Author + +Yanlan, Xie +Biotechnology and Engineering College, West Yunnan University, Lincang, 677000, China + + + +Author + +Yanli, Zhou +The Germplasm Bank of Wild Species, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, 650201, China + + + +Author + +Hongrui, Zhang +https://orcid.org/0000-0002-0089-1099 +Plant Protection College, Yunnan Agricultural University, Kunming, 650201, China +hongruizh@126.com + +text + + +Biodiversity Data Journal + + +2021 + +2021-11-24 + + +9 + + +72670 +72670 + + + + +http://dx.doi.org/10.3897/BDJ.9.e72670 + +journal article +http://dx.doi.org/10.3897/BDJ.9.e72670 +1314-2828-9-e72670 +705F74B63C8850A08D6DBA243535218D + + + + +Ayyaria chaetophora Karny, 1926 + + + + +Bussothrips claratibia +Moulton, 1935: 475 + + +Parafrankliniella fasciatus +Kurosawa, 1937: 271 + + +Parafrankliniella subfasciatus +Kurosawa, 1968: 24. + + + +Materials + + +Type status: + +Other material +. + +Occurrence +: + +recordedBy: + +L.Y. +J, S.S.Q, & E.N + +; individualID: +2019-II-16 +| +2017-III-11 +; individualCount: +2 +; sex: +females +; lifeStage: +adults +; occurrenceID: YAU5082020 +Tt +46; + +Taxon +: + +scientificNameAuthorship: +Ayyaria +chaetophora +Karny +; + +Location +: + +country: +China +; stateProvince: +Yunnan +; municipality: +Xishuangbanna +; locality: + +Mengla +(Tropical Botanical Garden) + +; decimalLatitude: +21.959819 +; decimalLongitude: +100.460016 +; + +Identification +: + +identifiedBy: + +Li Yajin + +; dateIdentified: 2018; identificationReferences: (ThripsWiki 2020); + +Event +: + +samplingProtocol: +sweeping and shaking +; eventDate: +11/03/2017 +, +16/02/2019 +; + +Record Level +: + +collectionID: thrips; institutionCode: YAU5082020; collectionCode: terebrantia; basisOfRecord: preserved specimen + + + + + +Ecological interactions + + +Feeds on + +leaves, collected from + +Litchi chinensis + +and mango. + + + +Distribution +Described from India. Recorded from Japan and China (Xishuangbanna). + + + \ No newline at end of file diff --git a/data/38/17/0E/38170EA566E20EDC6B182A77B28953E1.xml b/data/38/17/0E/38170EA566E20EDC6B182A77B28953E1.xml new file mode 100644 index 00000000000..70351f512ec --- /dev/null +++ b/data/38/17/0E/38170EA566E20EDC6B182A77B28953E1.xml @@ -0,0 +1,80 @@ + + + +Checklist of British and Irish Hymenoptera - aculeates (Apoidea, Chrysidoidea and Vespoidea) + + + +Author + +Else, George R. + + + +Author + +Bolton, Barry + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8050 +8050 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8050 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8050 +1314-2828-4-8050 + + + + +Episyron gallicum (Tournier, 1889) + + + + +Pompilus gallicus +Tournier, 1889 + + +intermedius +Haupt, 1930 + + +tertius +Bluethgen +, 1944 + + + +Distribution +England + + +Notes + +added by +Baldock (2006) + + + + \ No newline at end of file diff --git a/data/38/17/7D/38177D874B4D5F81996CDFA479D8959A.xml b/data/38/17/7D/38177D874B4D5F81996CDFA479D8959A.xml new file mode 100644 index 00000000000..0e49b174561 --- /dev/null +++ b/data/38/17/7D/38177D874B4D5F81996CDFA479D8959A.xml @@ -0,0 +1,193 @@ + + + +Three new species of caddisflies (Trichoptera, Hydroptilidae, Polycentropodidae, Leptoceridae) from Khon Phapheng Waterfall, the Mekong River, Laos + + + +Author + +Thamsenanupap, Penkhae +Faculty of Environment and Resource Studies, Mahasarakham University, Mahasarakham Province, Thailand + + + +Author + +Malicky, Hans +Sonnengasse 13, A- 3293 Lunz am See, Austria + + + +Author + +Vongsombath, Chanda +Faculty of Environmental Sciences, National University of Laos, Dong Dok Campus, Vientiane, PDR, Laos + + + +Author + +Laudee, Pongsak +https://orcid.org/0000-0003-3819-7980 +Faculty of Innovative Agriculture and Fishery Establishment Project, Prince of Songkla University, Surat Thani Campus, Muang District, Surat Thani Province, Thailand +pongsak.l@psu.ac.th + +text + + +ZooKeys + + +2021 + +2021-08-12 + + +1055 + + +149 +159 + + + + +http://dx.doi.org/10.3897/zookeys.1055.66536 + +journal article +http://dx.doi.org/10.3897/zookeys.1055.66536 +1313-2970-1055-149 +0A16D86E946F4E2698B5FAB2AC33645F +CFDE91ABE2175C05A56157CEB93A6E75 + + + + +Pseudoneureclipsis khonphaphengensis Malicky & Thamsenanupap +sp. nov. + + + + +Figure 2 + + + +Type material. + + +Holotype +. Male. Laos: Pakse Province + +: Champasak, Khonphapheng waterfall, Mekong river, +13°57'30"N +, +105°59'14"E +, elev. 64 m, 8.iv.2019, Pongsak Laudee. (PSUNHM). +Paratypes +: same data as the holotype; +Laos: Vientiane province +: Nam Lik river, +18°31'29"N +, +102°31'19"E +, elev. 180 m, 8.iv.2019, Pongsak Laudee. 9 males: 2 males (PSUNHM), 3 males (CHM), 2 males (NMPC), 2 males (CUAC). + + + +Diagnosis. + +The male genitalia of + +P. khonphaphengensis + +sp. nov. are similar to those of + +P. kaineus + +Malicky & Bunlue in +Malicky et al. 2004 +from Thailand. However, + +P. khonphaphengensis + +sp. nov. is strikingly different from + +P. kaineus + +and the other species of the genus by the usually broad, almost circular inferior appendages with 1.5 +x +longer than its width in lateral view, while the inferior appendages of + +P. kaineus + +are oval and 3.2 +x +longer than its width in lateral view. In addition, the phallus of + +P. khonphaphengensis + +sp. nov. bearing the hooked phallic sclerite which are lacking in + +P. kaineus + +. + + + +Description. +Adult, male, length of each male forewing 4.0-4.5 mm (n = 9); general body color in alcohol yellow brown. + +Male genitalia as in Figure +2A-E +. Segment IX narrow in lateral view, with anterior margin produced forward in ca. 100° angle. (Fig. +2B +). Segment X bilobed, blunt apically in dorsal view; finger like with setae in lateral view. Preanal appendages, long, slender with setae, rounded apically in dorsal view and lateral view (Fig. +2A, B +). Intermediate appendages hooked and turned dorsally then bend outward immediately in dorsal view (Fig. +2A +); in lateral view hooked, slightly curved upward, pointed apically (Fig. +2B +). Inferior appendages strikingly broad and rounded, total length <2 +x +of its subapical width in lateral view (Fig. +2B +); slender oviform, total length <2 +x +of its width in ventral view (Fig. +2C +). Basodorsal processes of inferior appendages curved with strong setae dorsomedially, pointed apically in lateral view (Fig. +2B +); in ventral view, horn like, originated basodorsally, curved inward, each with tapering apex (Fig. +2C +). Phallus, long, cylindrical, bulbous basally, straight laterally with hooked phallic sclerite intermediately, with numerous subapical spines in lateral view and dorsal view (Fig. +2D, E +). + + + +Etymology. +The species is named for the type locality, Khon Phapheng waterfall. + + +Figure 2. + +Pseudoneureclipsis khonphaphengensis + +, sp. nov. Male genitalia +A +segment X, preanal appendages and intermediate appendages, dorsal +B +segments IX and X and inferior appendages, left lateral +C +inferior appendages, ventral +D +phallus, left lateral; the arrow shows hooked phallic sclerite, ventral +E +phallus, dorsal. Abbreviations: Seg IX = segment IX, Seg X = segment X, Pre = preanal appendages, Int = Intermediate appendage, Inf = inferior appendage (paired), Bas = basodorsal process of inferior appendage. + + + + + \ No newline at end of file diff --git a/data/38/17/7D/38177D90E3FB30CCB8BD1628D7681FCC.xml b/data/38/17/7D/38177D90E3FB30CCB8BD1628D7681FCC.xml new file mode 100644 index 00000000000..c69d6ce4907 --- /dev/null +++ b/data/38/17/7D/38177D90E3FB30CCB8BD1628D7681FCC.xml @@ -0,0 +1,100 @@ + + + +Checklist of British and Irish Hymenoptera - Sawflies, ' Symphyta' + + + +Author + +Liston, Andrew D. + + + +Author + +Knight, Guy T. + + + +Author + +Sheppard, David A. + + + +Author + +Broad, Gavin R. + + + +Author + +Livermore, Laurence + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1168 +1168 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1168 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1168 +1314-2828-2-1168 + + + + +Arge rustica (Linnaeus, 1758) + + + + +Tenthredo rustica +Linnaeus, 1758 + + +Tenthredo atrata +(Forster, 1771, +Tenthredo +) + + +Cryptus segmentaria +(Panzer, 1803, +Cryptus +) + + +Hylotoma klugii +(Leach, 1817, +Hylotoma +) + + +Hylotoma leachii +(Stephens, 1835, +Hylotoma +) + + + +Distribution +England + + + \ No newline at end of file diff --git a/data/38/18/42/3818428E81AF3B2BB80FB8EB0F0DAEA4.xml b/data/38/18/42/3818428E81AF3B2BB80FB8EB0F0DAEA4.xml new file mode 100644 index 00000000000..98f8e2d6836 --- /dev/null +++ b/data/38/18/42/3818428E81AF3B2BB80FB8EB0F0DAEA4.xml @@ -0,0 +1,596 @@ + + + +Info Flora Schweiz - Poaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/poaceae.html + +url + + + + + +Holcus mollis +L. + + + + + +Weiches Honiggras + + + + +Art ISFS: 206900 Checklist: 1023640 +Poaceae +Holcus +Holcus mollis L. + + +Zusammenfassung + + + + +Artbeschreibung + +(nach +Lauber & al. 2018 +) + +: Unterscheidet sich von + +H. lanatus + +durch folgende Merkmale: + +Pflanze kahl oder zerstreut behaart, nur die Knoten +baertig + +, +Blaetter +deutlich rau, +Blatthaeutchen +nur am Rand fein bewimpert. +Blattscheiden nicht aufgeblasen +, +Huellspelzen +gelblich, nur auf dem Kiel rau, Deckspelze der oberen +Bluete + +mit geknieter, die +Huellspelze +etwa um 1/3 +ueberragender +Granne + +. + + + + +Bluetezeit + +(nach +Lauber & al. 2018 +) + +: 6-7 + + +Standort und Verbreitung in der Schweiz + +(nach +Lauber & al. 2018 +) + +: Naturwiesen, +Aecker +, lichte +Waelder +/ kollin-montan(-subalpin) / CH (fehlt im Engadin) + + + + +Verbreitung global + +(nach +Lauber & al. 2018 +) + +: +Europaeisch + + + + +Oekologische +Zeigerwerte + +(nach +Landolt & al. 2010 +) + +3w22-33 + 2.h.2n=14,28,35,42(49) + + + +Status + + + +Status IUCN +: Nicht +gefaehrdet + + + +Anatomie + +Zusammenfassung +der Blattanatomie Obere Epidermiszellen gleich gross wie untere. Epidermis mit Papillen. Verbindungs-Steg zwischen oberer und unterer Epidermis homogen verholzt. +Leitbuendel +im Verbindungs-Steg in der Mitte eingebettet. +Leitbuendelhuelle +verholzt. + + +Zusammenfassung der Stammanatomie + + +Umriss rund oder oval. +Leitbuendel +in einer Reihe. Epidermiszellen verholzt. Chlorenchyma in peripheren runden, ovalen oder rechteckigen Gruppen. + + +Beschreibung (Englisch) + + +Culm-diameter +2-5 mm +, wall thin, radius of culm in relation to wall thickness approximately 1:0.25 or <0.25. Outline circular with a smooth surface. Culm-center hollow and surrounded by many large thin-walled, not lignified cells. Epidermis-cells thick-walled all around. Large vascular bundles arranged in 2-3 peripheral rows. Chlorenchyma in round, oval, square or rectangular groups. Sclerenchyma in a large, peripheral continuous belt (> 3 cells). Cells thick-walled. Girders square, rectangular or conic. Small sclerenchymatic sheath with 1-2 cells around vascular bundles. Largest vessels in vascular bundles in lateral position. Largest vessel in the bundle 20-50 +μm +. + + + +Oekologie + + + +Lebensform +Mehrjaehriger +Hemikryptophyt + + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + + + + + + + + + + + + + + +
+5.1.2 - Mesophiler Krautsaum ( +Trifolion medii +) +
+5.2.2 - Kalkarme Schlagflur ( +Epilobion angustifolii +) +
+6.3.6 - Saurer Eichenmischwald ( +Quercion robori-petraeae +) +
6.3.7 - Kastanienwald
+
+ + +fett + +Dominante Art, welche das Aussehen des Lebensraumes +mitpraegt + +Charakterart +Weniger strikt an den Lebensraum gebundene Art + + +
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +maessig +feucht; Feuchtigkeit +maessig +wechselnd ( ++/- +1-2 Stufen) +Lichtzahl LhalbschattigSalzzeichen--
Reaktionszahl Rsauer (pH 3.5-6.5)Temperaturzahl Tunter-montan und ober-kollin
+Naehrstoffzahl +N + +naehrstoffarm + +Kontinentalitaetszahl +K +subozeanisch (hohe Luftfeuchtigkeit, geringe Temperaturschwankungen, eher milde Winter)
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Holcus mollis +L. + + + + + + +Volksname Deutscher Name: +Weiches Honiggras +Nom +francais +: +Houque molle +Nome italiano: +Bambagione aristato + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Holcus mollis L. + + +Checklist 2017 + +206900
= +Holcus mollis L. + + +Flora Helvetica 2001 + +2728
= +Holcus mollis L. + + +Flora Helvetica 2012 + +2908
= +Holcus mollis L. + + +Flora Helvetica 2018 + +2908
= +Holcus mollis L. + + +Index synonymique 1996 + +206900
= +Holcus mollis L. + + +Landolt 1977 + +239
= +Holcus mollis L. + + +Landolt 1991 + +220
= +Holcus mollis L. + + +SISF/ISFS 2 + +206900
= +Holcus mollis L. + + +Welten & Sutter 1982 + +2302
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Status Indigenat +: Indigen + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein + + +Status Rote Liste national 2016 + + +Status IUCN +: Nicht +gefaehrdet + + + +Zusaetzliche +Informationen + +Kriterien IUCN: -- + + +Status Rote Liste regional 2019 + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Biogeografische RegionenStatusKriterien IUCN
Jura (JU) +nicht +gefaehrdet +(Least Concern) +
Mittelland (MP) +nicht +gefaehrdet +(Least Concern) +
Alpennordflanke (NA) +nicht +gefaehrdet +(Least Concern) +
+Alpensuedflanke +(SA) + +nicht +gefaehrdet +(Least Concern) +
+Oestliche +Zentralalpen (EA) + +potenziell +gefaehrdet +(Near Threatened) +B2b(iii)
Westliche Zentralalpen (WA) +potenziell +gefaehrdet +(Near Threatened) +B2b(iii)
+
+ + +Status nationale +Prioritaet +/Verantwortung + + + + + + + +
+Keine nationale +Prioritaet +oder internationale Verantwortung +
+
+ +Schutzstatus + + + + + + +
Kein internationaler, nationaler oder kantonaler Schutz
+
+
+
+
\ No newline at end of file diff --git a/data/38/18/7E/38187E734E0259DEA53BA639DFFF7369.xml b/data/38/18/7E/38187E734E0259DEA53BA639DFFF7369.xml new file mode 100644 index 00000000000..b56c2fd3c83 --- /dev/null +++ b/data/38/18/7E/38187E734E0259DEA53BA639DFFF7369.xml @@ -0,0 +1,98 @@ + + + +Annotated type catalogue of the Orthalicoidea (Mollusca, Gastropoda) in the Museum fuer Naturkunde, Berlin + + + +Author + +Breure, Abraham S. H. +Naturalis Biodiversity Center, P. O. Box 9517, 2300 RA Leiden, the Netherlands +bbreure@xs4all.nl + +text + + +ZooKeys + + +2013 + +2013-03-25 + + +279 + + +1 +101 + + + + +http://dx.doi.org/10.3897/zookeys.279.4701 + +journal article +http://dx.doi.org/10.3897/zookeys.279.4701 +1313-2970-279-1 +ED3DFF9E63233556F47FFFBEB35AFFBA +578213 + + + + + +Bulimus +(Eudioptus) psidii Martens, 1877 + + + + + +Bulimus (Eudioptus) psidii +Martens 1877 +: 351, pl. 12 fig. 6 + + +Simpulopsis (Eudioptus) psidii +; + +Koehler +2007 + +: 156. + + + +Remarks. + +Contrary to +Koehler's +remark, +Breure (1979) +did not list this taxon under + +Simpulopsis (Eudioptus) + +since he did not consider + +Bulimus (Eudioptus) psidii + +belonging to the +Bulimulidae +(then +Bulimulinae +) (Breure, unpublished data). Upon examination of the type specimens in the ZMB it became clear that +Martens' +taxon may be classified with + +Platysuccinea + +( +Sagdidae +). This has to be confirmed by further anatomical and phylogenetic studies. + + + + \ No newline at end of file diff --git a/data/38/18/AE/3818AEDF7E01DF992D33E445B528F3DC.xml b/data/38/18/AE/3818AEDF7E01DF992D33E445B528F3DC.xml new file mode 100644 index 00000000000..037af321eac --- /dev/null +++ b/data/38/18/AE/3818AEDF7E01DF992D33E445B528F3DC.xml @@ -0,0 +1,93 @@ + + + +Checklist of British and Irish Hymenoptera - Sawflies, ' Symphyta' + + + +Author + +Liston, Andrew D. + + + +Author + +Knight, Guy T. + + + +Author + +Sheppard, David A. + + + +Author + +Broad, Gavin R. + + + +Author + +Livermore, Laurence + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1168 +1168 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1168 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1168 +1314-2828--1168 +3C3EC7B09BA145848E3E89CBBD28B432 +3C3EC7B09BA145848E3E89CBBD28B432 + + + + + +Ametastegia tenera ( +Fallen +, 1808) + + + + + +Tenthredo tenera +Fallen +, 1808 + + +Tenthredo patellata +(Klug, 1818, +Tenthredo +) + + +Ametastegia tener +: misspelling + + + +Distribution +England, Scotland, Wales, Ireland + + + \ No newline at end of file diff --git a/data/38/18/B1/3818B1D50AA65B6784B0A60BB9FCF6E8.xml b/data/38/18/B1/3818B1D50AA65B6784B0A60BB9FCF6E8.xml new file mode 100644 index 00000000000..eb7d666ecb7 --- /dev/null +++ b/data/38/18/B1/3818B1D50AA65B6784B0A60BB9FCF6E8.xml @@ -0,0 +1,218 @@ + + + +Nomenclatural revision and typification of extra-Amazonian Tachigali (Leguminosae - Caesalpinioideae) + + + +Author + +Deccache, Lara Serpa Jaegge +https://orcid.org/0000-0001-5701-0224 +Escola Nacional de Botanica Tropical, Rio de Janeiro, Brazil & Instituto de Pesquisas Jardim Botanico do Rio de Janeiro, Rio de Janeiro, Brazil +larasjdeccache@gmail.com + + + +Author + +de Lima, Haroldo Cavalcante +https://orcid.org/0000-0003-2154-670X +Escola Nacional de Botanica Tropical, Rio de Janeiro, Brazil & Instituto de Pesquisas Jardim Botanico do Rio de Janeiro, Rio de Janeiro, Brazil & Instituto Nacional da Mata Atlantica, Santa Teresa, Brazil + + + +Author + +de Fraga, Claudio Nicoletti +https://orcid.org/0000-0003-1254-4550 +Escola Nacional de Botanica Tropical, Rio de Janeiro, Brazil & Instituto de Pesquisas Jardim Botanico do Rio de Janeiro, Rio de Janeiro, Brazil + +text + + +Plant Ecology and Evolution + + +2024 + +2024-04-26 + + +157 + + +2 + + +137 +148 + + + + +http://dx.doi.org/10.5091/plecevo.111072 + +journal article +http://dx.doi.org/10.5091/plecevo.111072 +2032-3921-2-137 +5C82B3D8E47C5547A8D27B36593759C5 + + + + +5. +Tachigali duckei (Dwyer) Oliveira-Filho (Oliveira-Filho 2006: 140) + + + + +Sclerolobium duckei +Dwyer ( +Dwyer 1957 +: 109) + + + + +Type +. + + + +BRAZIL +- + +Rio de Janeiro + +• +Itatiaia +, +Parque Nacional +, +Lote Hansen +, borda da mata com o +rocado +; +1 Oct. 1940 +; fl., fr.; + + +W. +Duarte de Barros + +48 + +; +lectotype +( +designated here +): RB n°45677 [3 sheets, RB00585813!, RB00585812!, RB00539707!]; +isolectotype +: SP [SP000943!] + +. + + + +Notes. + +Dwyer (1957) +indicated that the type material of + +S. duckei + +is deposited in herbarium R (T.: +Duarte de Barries 48 +(R)!). However, he refered to the Systematic Botany Section of the Botanical Garden of Rio de Janeiro as R, thus to the herbarium RB. The correction for the location of the type material is clarified in the present paper (see ICN Art. 9.2; +Turland et al. 2018 +). + + +The specimen deposited in RB under the number 45677 is composed of three sheets. The first of which has the original herbarium labels and a determination label written by Dwyer, together with a barcode (RB00539707; Fig. +3A +), and it is composed of two branches: one with leaves and the other with a leaf, inflorescence, and flowers. The second sheet (RB00585812; Fig. +3B +) has a duplicate distribution stamp (Fig. +3C +) indicating that the SP herbarium received one sample (Fig. +3D +), and it is composed of a branch with leaves and a fruit. The third sheet (RB00585813; Fig. +3E +) has a branch with two leaves and an envelope of fragments with leaflets, inflorescence side branches, flowers, and a fruit. The curator of the RB herbarium distributed part of the RB type collection to other herbaria in 2008 (Rafaela Campostrini Forzza pers. comm.), so the SP specimen was previously studied by Dwyer, making it impossible to consider the set deposited in RB to be seen as a holotype assembled in more than one preparation, as it is now only part of the whole. Therefore, the gathering located at RB under the number 45677 is chosen as the lectotype, as it is the complete material and what the author first designated. + + + +Figure 3. +Type specimens of + +Sclerolobium duckei + +, + +Sclerolobium friburgense + +, + +Cassia paratyensis + +, + +Sclerolobium pilgerianum + +, and + +Sclerolobium striatum + +. +A +, +B +, +E +. Lectotype designated for + +S. duckei + +. +C +. Stamp from the specimen of + +S. duckei + +with the designation of duplicates. +D +. Remaining syntype of + +S. duckei + +. +F +. Lectotype designated for + +S. friburgense + +. +G +. Lectotype designated for + +C. paratyensis + +. +H +. Lectotype designated for + +S. pilgerianum + +. +I +. Lectotype of + +S. striatum + +. + + + + + \ No newline at end of file diff --git a/data/38/19/45/38194517F9A3DDA9A876E96C5E95EC4D.xml b/data/38/19/45/38194517F9A3DDA9A876E96C5E95EC4D.xml new file mode 100644 index 00000000000..70229e99ce9 --- /dev/null +++ b/data/38/19/45/38194517F9A3DDA9A876E96C5E95EC4D.xml @@ -0,0 +1,71 @@ + + + +Cyanobacteria of Greece: an annotated checklist + + + +Author + +Gkelis, Spyros + + + +Author + +Ourailidis, Iordanis + + + +Author + +Panou, Manthos + + + +Author + +Pappas, Nikos + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +10084 +10084 + + + + +http://dx.doi.org/10.3897/BDJ.4.e10084 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e10084 +1314-2828--10084 + + + + +Chamaesiphon geitleri A. Braun in Rabenhorst, 1865 + + + + +Chamaesiphon geitleri + + + +Notes + +Anagnostidis 1968 + + + + \ No newline at end of file diff --git a/data/38/19/78/381978A37995DFF42DB2827C8FEA7DDA.xml b/data/38/19/78/381978A37995DFF42DB2827C8FEA7DDA.xml new file mode 100644 index 00000000000..64679391615 --- /dev/null +++ b/data/38/19/78/381978A37995DFF42DB2827C8FEA7DDA.xml @@ -0,0 +1,80 @@ + + + +Catalogue of Geadephaga (Coleoptera, Adephaga) of America, north of Mexico + + + +Author + +Bousquet, Yves +Agriculture and Agri-Food Canada, Central Experimental Farm, Ottawa, Ontario, Canada +bousquety1@yahoo.com + +text + + +ZooKeys + + +2012 + +2012-11-28 + + +245 + + +1 +1722 + + + + +http://dx.doi.org/10.3897/zookeys.245.3416 + +journal article +http://dx.doi.org/10.3897/zookeys.245.3416 +1313-2970-245-1 +FFFF52503A0AFF882450FFB66D45FF8E +578462 + + + + +Pterostichus obsidianus Casey, 1913 + + + + +Pterostichus obsidianus +Casey, 1913: 102. Type locality: "Monterey [Monterey County], California" (original citation). Lectotype (♂), designated by Bousquet (1999: 175), in USNM [# 46982]. + + + +Distribution. +This species is known only from the lectotype collected in coastal California. + + +Records. + +USA +: CA + + + +Note. + +The lectotype of + +Pterostichus obsidianus + +Casey is structurally similar to and possibly conspecific with members of + +Pterostichus scutellaris + +LeConte. + + + + \ No newline at end of file diff --git a/data/38/19/9B/38199BD9971122FB0389A9592E932BBE.xml b/data/38/19/9B/38199BD9971122FB0389A9592E932BBE.xml new file mode 100644 index 00000000000..edf86803d29 --- /dev/null +++ b/data/38/19/9B/38199BD9971122FB0389A9592E932BBE.xml @@ -0,0 +1,112 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part T) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +878 +905 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Triticum junceum +Linnaeus + +, + +Centuria I Plantarum + +: 6. 1755 + + +. + + + +"Habitat in Helvetia, Oriente." RCN: 725. + + + + + +Lectotype + +(Jarvie in +Nordic J. Bot. +12: 167. 1992; Jarvie in Cafferty & al. in +Taxon +49: 258. 2000): +Hasselquist +, Herb. Linn. No. 104.5 ( +LINN +; + +iso- + +104.6 +LINN +) + +. + + + + +Current name: + + +Elytrigia juncea + +(L.) Nevski + +( +Poaceae +). + + + + +Note: +Loeve +(in +Feddes Repert. +95: 476. 1984) stated +"... +quoad pl. lectotyp. Ab HASSELQUIST lectam", without indicating any sheet or location. Jarvie (in +Nordic J. Bot. +12: 167. 1992) indicated material at LINN as type, but did not distinguish between sheets 104.5 and 104.6 (which might well be part of a single gathering). Jarvie subsequently restricted his earlier choice to one of them, in accordance with Art. 9.15. + + + + \ No newline at end of file diff --git a/data/38/19/F4/3819F48CB222B55E8176FAE2000D9477.xml b/data/38/19/F4/3819F48CB222B55E8176FAE2000D9477.xml new file mode 100644 index 00000000000..d21c3ddf981 --- /dev/null +++ b/data/38/19/F4/3819F48CB222B55E8176FAE2000D9477.xml @@ -0,0 +1,142 @@ + + + +Order Scandentia + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +104 +109 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Tupaia montana +Thomas 1892 + + + + + + + +Tupaia montana +Thomas 1892 + +, +Ann. Mag. Nat. Hist., ser. 6, 9: 252 + +. + + + + +Type Locality: + +Borneo, +Sarawak +, Mt. Dulit, +5,000 ft. +( + +1,524 m + +). + + + + + +Vernacular Names: +Mountain Treeshrew +. + + + + +Subspecies: +: + + +Subspecies + +Tupaia montana +subsp. +montana +Thomas 1892 + + + +Subspecies + +Tupaia montana +subsp. +baluensis +Lyon 1913 + + + + + +Distribution: +Mountains of +Sarawak +and W +Sabah +( +Malaysia +); probably N +Kalimantan +( +Indonesia +). + + + + +Conservation: +CITES +– Appendix II; +IUCN +– Lower Risk (lc). + + + + +Discussion: +A Bornean montane endemic with two well-marked subspecies. + + + + \ No newline at end of file diff --git a/data/38/19/FF/3819FFAE8817B40A3D4A2CE109426534.xml b/data/38/19/FF/3819FFAE8817B40A3D4A2CE109426534.xml new file mode 100644 index 00000000000..55d517f57ca --- /dev/null +++ b/data/38/19/FF/3819FFAE8817B40A3D4A2CE109426534.xml @@ -0,0 +1,43 @@ + + + +Note sur les fourmis du Musée Zoologique de l'Académie Impériale des Sciences à St. Pétersbourg. + + + +Author + +Forel, A. + +text + + +Yezhegodnik Zoologicheskogo Muzeya Imperatorskoi Akademii Nauk + + +1904 + +8 + + +368 +388 + + + +journal article +3994 +10.5281/zenodo.25586 + + + + +Leptogenys truncatirostris Forel +. + + + +10 [[ worker ]]. Madagascar: Ranomafana et Fort Dauphin, 1899 (Sikora!). + + + \ No newline at end of file diff --git a/data/38/1A/18/381A181442FD8782C423CF47F941B093.xml b/data/38/1A/18/381A181442FD8782C423CF47F941B093.xml new file mode 100644 index 00000000000..75b7c3c09a8 --- /dev/null +++ b/data/38/1A/18/381A181442FD8782C423CF47F941B093.xml @@ -0,0 +1,78 @@ + + + +Checklist of British and Irish Hymenoptera - Sawflies, ' Symphyta' + + + +Author + +Liston, Andrew D. + + + +Author + +Knight, Guy T. + + + +Author + +Sheppard, David A. + + + +Author + +Broad, Gavin R. + + + +Author + +Livermore, Laurence + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1168 +1168 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1168 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1168 +1314-2828--1168 +3C3EC7B09BA145848E3E89CBBD28B432 +3C3EC7B09BA145848E3E89CBBD28B432 + + + + +Nematus Panzer, 1801 + + + + +HYPOLAEPUS +W. F. Kirby, 1882 + + +HOLCOCNEME +Konow, 1890 + + + + \ No newline at end of file diff --git a/data/38/1A/87/381A877B66B75A9EA500720B87FB2D3B.xml b/data/38/1A/87/381A877B66B75A9EA500720B87FB2D3B.xml new file mode 100644 index 00000000000..c71c30981c1 --- /dev/null +++ b/data/38/1A/87/381A877B66B75A9EA500720B87FB2D3B.xml @@ -0,0 +1,68 @@ + + + +Catalogue of Geadephaga (Coleoptera, Adephaga) of America, north of Mexico + + + +Author + +Bousquet, Yves +Agriculture and Agri-Food Canada, Central Experimental Farm, Ottawa, Ontario, Canada +bousquety1@yahoo.com + +text + + +ZooKeys + + +2012 + +2012-11-28 + + +245 + + +1 +1722 + + + + +http://dx.doi.org/10.3897/zookeys.245.3416 + +journal article +http://dx.doi.org/10.3897/zookeys.245.3416 +1313-2970-245-1 +FFFF52503A0AFF882450FFB66D45FF8E +578462 + + + + +Subgenus +Dicaelus Bonelli, 1813 + + + + +Dicaelus +Bonelli, 1813: 446. Type species: + +Dicaelus violaceus + +Bonelli, 1813 (= + +Dicaelus purpuratus + +Bonelli, 1813) designated by Hope (1838: 82). + + + +Diversity. +Six North American species, one of them extending into northern Mexico, arrayed in three species groups. + + + \ No newline at end of file diff --git a/data/38/1A/D9/381AD9DCCE41E608A31ECD5EC95065F7.xml b/data/38/1A/D9/381AD9DCCE41E608A31ECD5EC95065F7.xml new file mode 100644 index 00000000000..e788ff1cb07 --- /dev/null +++ b/data/38/1A/D9/381AD9DCCE41E608A31ECD5EC95065F7.xml @@ -0,0 +1,50 @@ + + + +H. Sauter's Formosa-Ausbeute: Formicidae (Hym.). + + + +Author + +Forel, A. + +text + + +Entomologische Mitteilungen + + +1912 + +1 + + +45 +81 + + + + +http://antbase.org/ants/publications/4035/4035.pdf + +journal article +4035 + + + + +Discothyrea globus Forel v. Sauteri +n. Var. + + + + +[[worker]] L. 1,6 bis 1,8 mm, Etwas groesser als der Arttypus aus Java. Augen mit 6-10 Fazetten. Erstes Geisselglied nicht doppelt so dick als lang. Thoraxruecken etwas konvexer, doppelt so lang als breit, gar nicht gerandet. Epinotum mit recht kleinen, aber deutlichen dreieckigen Zaehnchen, Stielchen ebenso verwachsen, aber oben hoechstens dreimal breiter als lang, unten nur mit einem kuerzeren Vorsprung. Kopf so breit als lang, mit sehr konvexen Seiten (kaum konvex bei +antarctica +). Sonst wie der Arttypus. Vielleicht eigene Rasse oder Subspecies. + +[[queen]] L. 2,1 mm. Kopf hinten breiter als vorn. Fluegel fehlen, Epinotumzaehne breiter als beim [[worker]]. Sonst wie der [[worker]]. Pilam. + + + \ No newline at end of file diff --git a/data/38/1A/F6/381AF6204A4E44979A4B4DFE6708FEDD.xml b/data/38/1A/F6/381AF6204A4E44979A4B4DFE6708FEDD.xml new file mode 100644 index 00000000000..3ca01db5e68 --- /dev/null +++ b/data/38/1A/F6/381AF6204A4E44979A4B4DFE6708FEDD.xml @@ -0,0 +1,48 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828--9042 + + + + +Limerodops Heinrich, 1949 + + + + +OXYSOMA +Kriechbaumer, 1875 preocc. + + + + \ No newline at end of file diff --git a/data/38/1B/15/381B15F519CBA6E379A76A301CF5EE8E.xml b/data/38/1B/15/381B15F519CBA6E379A76A301CF5EE8E.xml new file mode 100644 index 00000000000..692b1866319 --- /dev/null +++ b/data/38/1B/15/381B15F519CBA6E379A76A301CF5EE8E.xml @@ -0,0 +1,59 @@ + + + +Species plantarum: exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas + + + +Author + +Linnaeus, Carolus + +text + +1753 +Laurentius Salvius + +Stockholm + + + +https://doi.org/10.5962/bhl.title.669 + +book +10.5281/zenodo.3931989 +3931989 + + + + +Iris tuberosa +, +spec. nov. + + + + +15. Iris corollis imberbibus, foliis tetragonis. +Vir. cliff.6. Hort cliff. 20. Mat. med. 26. Roy. lugdb.18. + + +Iris tuberosa, folio anguloso. +Bauh. pin. 40. + + +Hermodactylus folio quadrangulo. +Tournef. cor. 50. + + + + +Habitat in +Arabia +& +Oriente +. ♃ + + + + \ No newline at end of file diff --git a/data/38/1C/29/381C299722705D678A8310E3320BC8D9.xml b/data/38/1C/29/381C299722705D678A8310E3320BC8D9.xml new file mode 100644 index 00000000000..4f554cb78cd --- /dev/null +++ b/data/38/1C/29/381C299722705D678A8310E3320BC8D9.xml @@ -0,0 +1,93 @@ + + + +Updated checklist of polychaete species (Annelida) recorded from Malaysia, with remarks on the research history + + + +Author + +Razmi Shah, Raz Shauqeena Batrisyea +Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, 21030, Kuala Nerus, Kuala Terengganu, Malaysia + + + +Author + +Ibrahim, Yusof Shuaib +Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, 21030, Kuala Nerus, Kuala Terengganu, Malaysia +yusofshuaib@umt.edu.my + + + +Author + +Villalobos-Guerrero, Tulio F. +https://orcid.org/0000-0001-9691-8200 +Department of Marine Ecology, Centro de Investigacion Cientifica y de Educacion Superior de Ensenada, 22860, Ensenada, Baja California, Mexico + + + +Author + +Sato, Masanori +Department of Earth and Environmental Sciences, Graduate School of Engineering and Science, Kagoshima University, 1 - 21 - 35 Korimoto, 890 - 0065, Kagoshima, Japan + +text + + +Biodiversity Data Journal + + +2023 + +2023-10-19 + + +11 + + +110021 +110021 + + + + +http://dx.doi.org/10.3897/BDJ.11.e110021 + +journal article +http://dx.doi.org/10.3897/BDJ.11.e110021 +1314-2828-11-e110021 +0C949EDF297654B5BB85F8E8BCC0A5D8 + + + + +Prionospio sp. + + + +Distribution + +Distribution in Malaysia. Teluk Aling, Penang ( +Ong 1995 +, +Idris and Arshad 2013 +). + + + +Notes + +It showed similar features to + +P. malmgreni + +Claparede +, 1869; however, the author, +Ong (1995) +needed clarification and samples were undetermined. + + + + \ No newline at end of file diff --git a/data/38/1D/14/381D14FA8BEA48F78477394839173B4E.xml b/data/38/1D/14/381D14FA8BEA48F78477394839173B4E.xml new file mode 100644 index 00000000000..f22a9c03b0c --- /dev/null +++ b/data/38/1D/14/381D14FA8BEA48F78477394839173B4E.xml @@ -0,0 +1,219 @@ + + + +A new genus and three new species of noctuid moths from western United States of America and Mexico (Lepidoptera, Noctuidae, Noctuinae, Eriopygini) + + + +Author + +Crabo, Lars G. + +text + + +ZooKeys + + +2018 + +788 + + +183 +199 + + + + +http://dx.doi.org/10.3897/zookeys.788.26068 + +journal article +http://dx.doi.org/10.3897/zookeys.788.26068 +1313-2970-788-183 +21EE3AE1CBAC41A5A08C8420E132F63C +21EE3AE1CBAC41A5A08C8420E132F63C + + + + +Rhabdorthodes pattersoni +sp. n. +Figs 1-4, 7, 10, 13, 16 + + + +Type locality. +USA: Colorado: Clear Creek County: Doolittle Ranch, Mt. Evans, 2987 m. + + +Type material. + +Holotype, male. USA: Colorado: [Clear Creek County]: Doolittle Ranch, Mt. Evans, 9,800' [2987 m], 10 VIII 1961, E. W. Rockburne. / Specimen ID CNCLEP 00140423. CNC. Paratypes. 49 m, 5 f. USA: Arizona: Apache County: Alpine, 3-5 mi [4.8-8.0 km] SE, 16 VI 1967 (1 m); Greer, White Mts., 8500' [2591 m], 6 VIII 1962, E. & I. Munroe, black light (1 m); same collection label / Genitalia slide # 11,732 male (1 m); [Greenlee County], Hannagan Meadow, 13 VI 1967, R. F. Sternitzky / Genitalia CNC slide # 17406 female (1 f); same collection label / [CNC] Slide No. 11,734 (1 m); Colorado: Archuleta County: [north of Pagosa Springs], 8[000]' [2438 m.], 15 VI 2004, Vargo leg. / Specimen ID CNCLEP 00120092 (1 m); same collection label / Specimen ID CNCLEP 00120092 (1 f); [Boulder County]: Boulder, Silver Saddle Motel, 5500' [1676 m], 5 VI 1961, M. R. MacKay (1 m); [Clear Creek County]: Doolittle Ranch, Mt. Evans, 9800' [2987 m], 16 VII 1961, E. W. Rockburne / Genitalia CNC slide # 15894 male (1 m); same collection label, 30 VII 1961 (1 m); same collection label / [CNC] Slide No. 10,766 female (1 f); same locality & collector, 31 VII 1961 (4 m); same collection label / [CNC] Slide No. 10,764 male (1 m); same locality & collector, 1 VIII 1961 (8 m); same locality and collector, 2 VIII 1961 (6 m); same collection label / Genitalia CNC slide # 15893 male (1 m); same locality & collector, 3 VIII 1961 (1 m); same locality & collector, 5 VIII 1961 (1 m); same locality & collector, 6 VIII 1961 (1 m); same locality & collector, 6 VIII 1961 (1 m); same locality & collector, 8 VIII 1961 (1 m); Teller County: Florissant, 3.5 mi [5.6 km] SW, 38.904° -105.323°, 8-9 VII 2016, 2660 m, L. G. Crabo & G. Morrell leg. (4 m); Idaho: Bear Lake County: Georgetown Cyn., 42.524° -111.263°, 2100 m, 4 VII 2016, L. G. Crabo & G. Morrel leg. / Specimen ID CNCLEP00140350 / Barcode +of +Life Project, Leg removed, DNA extracted (1 m); New Mexico: Colfax County: Cimarron Canyon, Sangre de Cristo Mts., 7900' [2408 m], 6 VII 1982, black light, E. & I. Munroe (1 m); same collection label / [CNC] slide No. 11733 male (1 m); same locality & collector, 8 VII 1962 (1 m); same locality & collector, 11 VII 1962 (1 m); Lincoln County: Capitan Mts., Capital Ridge, radio towers, summit, 10,000' [3048 m], 3 VII 1982, RWH [Ronald H. Hodges] (2 m); same locality & collector, 10 VII 1982 / Genitalia slide # 17407 female (1 f); Otero County, High Rolls, Karr Cyn., 32.898° -105.813°, 2400 m, 9 VI 2016, L. G. Crabo leg. (1 f); Sandoval County: San Jose Ca[illegible]., 4 mi [6.4 km] E. Regina, Jemez Mts., NW slope, 8500' [2591 m], 26 June, 1983, UV, RWH [Richard W. Holland] (1 m); Utah: [Iron County]: Cedar City, 11 mi [17.7 km] SE, 8300' [2530 m], 29 VIII 1965, D. F. Hardwick (1 m); Sanpete County: Ephraim, 8 mi [12.9 km] E, 39.317°-[39.]337° -111.448°-[111.]470°, 10000' [3048 m], 21 VII 2006, L. G. Crabo leg. / Specimen ID CNCLEP00140348/Barcode of Life Project, Leg removed, DNA extracted (1 m); same collection label / Specimen ID CNCLEP00140349 / Barcode of Life Project, Leg removed, DNA extracted (1m); Wyoming: Albany County: T13N R77W, Section 4, 1.5 mi (2.6 km) NW of Woods Landing, Fox Creek, el. 7,600 ft (2316 m), 21 VI 1997, black light trap, J. S. Nordin leg. (1 m): CNC, LGC, TM. + + + +Figures 1-6. +Rhabdorthodes +adults 1 +R. pattersoni +, holotype male, USA, Colorado, Clear Creek County, Doolittle Ranch, Mt. Evans 2 +R. pattersoni +, paratype male, USA, Colorado, Teller County, Florissant, 5.6 km SW 3 +R. pattersoni +, paratype male, USA, Utah, Sanpete County, Ephraim, 12.9 km E 4 +R. pattersoni +, paratype female, USA, Colorado, Archuleta County, Pagosa Springs 5 +R. durango +, holotype male, Mexico, Durango, El Salto 6 +R. petersoni +, holotype male, Mexico, Nuevo +Leon +, Cerro Potosi. + + + + +Diagnosis. + +Rhabdorthodes pattersoni +is the most drab and poorly patterned of the three +Rhabdorthodes +species, appearing dull dark brown with faint markings. The forewing subterminal line of +R. pattersoni +is faint pale gray, whereas those of the Mexican species are more prominent, luteous preceded by dark wedge-shaped spots. +Rhabdorthodes pattersoni +is the only species in the genus that is known to occur in the United States. + + +Structurally, males of +R. pattersoni +are distinguished from the Mexican species by the smaller ventral process of the distal clasper (Figure 7), relatively short and triangular. In both other species this process is longer and curves toward the apex of the valve. + +The shape of sternite A7 is shallowly concave with a quadrate lateral margin (Fig. 13). Those of the two Mexican species are more complex, with distinct lateral flanges, deeper pits, and more strongly concave edges (Figs 14, 15). + +The Barcode Index Number (BIN) of +R. pattersoni +from Colorado and Utah (n = 5) is BOLD:ADH0770. + + +This moth resembles several nondescript brown species of +Eriopygini +- such as species of +Homorthodes +McDunnough and +Protorthodes +- but is probably most similar superficially to " +Orthosia +" noverca (Grote), a common widespread western North American moth that lacks a satisfactory generic placement. Most " +O. +" noverca have thicker and more prominent black forewing pattern elements than those of +R. pattersoni +. +Rhabdorthodes +can be identified without dissection by observing the ends of the valves for the chunky claspers in males and the sculpted seventh sternite in females. In addition, males of +Rhabdorthodes +have biserrate antennae, simple in look-alikes other than +Protorthodes +. + + + +Figures 7-9. +Rhabdorthodes +male genitalia, valves and phalluses with everted vesicas 7 +R. pattersoni +8 +R. durango +9 +R. petersoni +. + + + + +Description. + +Adults.Head. Male antenna total width 3 +x +shaft; dorsal scales dark gray-brown, scattered off-white on proximal ⅓. Labial palpus scales gray-brown, scat +tered +off-white on second and third segments, increasing toward tip. Frons scales gray brown; dorsal head scales white tipped gray-brown. + + +Thorax. Dorsal scales long, white tipped gray-brown; appearing uniform dull gray-brown to dark brown. Wings: Forewing length 13.0-13.5 mm (males); 13.5 mm (females); scales gray-brown, scattered white tipped gray-brown, appearing uniform gray-brown to dark brown; costa spots luteous gray; basal, antemedial, and postmedial lines double, black and dark gray-brown, filling ground and slightly lighter gray; basal line uneven, indistinct; antemedial line slightly irregular, pointed basad on veins; medial line slightly darker than ground, angled distad from mid costa to reniform stigma, thence basad to posterior margin; postmedial line indistinct, evident mostly as black inner part and pale gray filling, scalloped; subterminal line irregular off-white patches between veins, preceding shade faint, brown; terminal line thin, dark gray; fringe striped dark gray, base thin, pale; orbicular stigma round, often incomplete, black, lined with few pale-gray scales, center ground color; claviform stigma small, black, filled with ground color, or reduced to a spot; reniform stigma moderate size, weakly figure-8 shaped, open at posterior end, black, with adjacent luteous and pale-gray lining strongest at medial and lateral sides, center ground color. Hindwing: Dorsum gray, +basal +1/2 +paler; veins and faint discal spot dark; terminal line thin, black; fringe gray with copper luster, base thin, pale. + + +Abdomen. Male genitalia: (Figure 7) Uncus length 0.9 +x +juxta. Juxta height 2 +x +width, rod length 1.2 +x +height. Valve length 5 +x +width, part distal to clasper curved slightly dorsad; cucullus weak, paddle shaped; sacculus length 0.5 +x +and width 0.75 +x +valve; distal clasper 1 +x +valve width, left slightly larger than right, thick, mesial surface with molar like ridges, dorsal distal margin expanded to broad rounded projection, ventral distal margin triangular with slight curve distad; ampulla directed 45° basad, scythe shaped with 120-180° curve distad; digitus small, thin. Phallus and vesica as in genus description. Female genitalia (Figs 10, 13): Sternite A7 lateral concavity shallow with quadrate raised lateral margin; posterior margin weakly concave. Papilla analis, segment A8, and bursa copulatrix as in genus description. + + + +Figures 10-12. +Rhabdorthodes +female genitalia 10 +R. pattersoni +11 +R. durango +12 +R. petersoni +. + + + + +Etymology. +I am pleased to name this moth after Robert (Bob) Patterson of Bowie, Maryland in recognition of his contribution to the study and enjoyment of North American moths through his work on the Moth Photographers Group website (http://mothphotographersgroup.msstate.edu). + + +Distribution and ecology. + +Rhabdorthodes pattersoni +occurs in the mountains of the American West (Figure 16). It has been collected from southeastern Idaho and south-central Wyoming in the north to southwestern Utah, eastern Arizona and south-central New Mexico in the south. Most records are from Colorado and New Mexico. It flies in mid- to high-elevation forest at elevations from 1600 to 3050 meters. Collection dates range from early June to early August. The early stages are unknown. + + + +Remarks. + +This species is moderately common in collections. Specimens are often mixed in with other brown species in the tribe +Eriopygini +, often " +Orthodes +" noverca and " +Orthodes +" obscura (Smith). + + + +Figures 13-15. +Rhabdorthodes +females. Distal abdomen (scales removed), left ventrolateral aspect showing sculpted sternite A7. 13 +R. pattersoni +14 +R. durango +15 +R. petersoni +. + + + + + \ No newline at end of file diff --git a/data/38/1D/64/381D64D39FD62BB3CE5EACA8D733069F.xml b/data/38/1D/64/381D64D39FD62BB3CE5EACA8D733069F.xml new file mode 100644 index 00000000000..527e5ebe963 --- /dev/null +++ b/data/38/1D/64/381D64D39FD62BB3CE5EACA8D733069F.xml @@ -0,0 +1,187 @@ + + + +Subgenera of Charidotella Weise with description of a new subgenus and species from Brazil (Coleoptera, Chrysomelidae, Cassidinae, Cassidini) + + + +Author + +Sekerka, Lukas + + + +Author + +Borowiec, Lech + +text + + +ZooKeys + + +2015 + +506 + + +61 +74 + + + + +http://dx.doi.org/10.3897/zookeys.506.8770 + +journal article +http://dx.doi.org/10.3897/zookeys.506.8770 +1313-2970-506-61 +BD777FC26CB843B7AE342FBFEC620025 + + + +Taxon classification Animalia Coleoptera Chrysomelidae + + + +Xenocassis Spaeth, 1936 +Figs 12-13 + + + + +Xenocassis +Spaeth, 1936: 260; +Hincks 1952 +: 342 (as subgenus of +Charidotella +). + + + +Type species. + +Coptocycla amoena +Boheman, 1855 by original designation. + + + +Number of species. +15 (present paper). + + +Key to species. +Not yet proposed. + + +Range. +Mexico to Peru with most species in the Central America. + + +Distinguishing characters. + +Xenocassis +species can be easily separated from other subgenera by the small eyes covering only 2/3 of lateral sides of the head thus gena is well visible while all other subgenera have large eyes. In addition +Xenocassis +has nearly regularly circular body outline, weakly convex elytra with coarser punctation on lateral slope, and dorsum with ring pattern on the upper side. In extreme cases the ring can form a large discal spot or can be completely vanished thus whole dorsum is uniformly yellow. + + + +Remarks. + +So far +Xenocassis +was separated from other genera on the basis of the tarsal claws and general body shape. +Windsor et al. (1992) +were the first who noticed that all species have also small eyes in comparison to other +Chardotella +species. As a result they raised +Xenocassis +to genus in the provided key but unfortunately made no additional comments and their change was not accepted later (e.g. +Borowiec 1999 +). We agree with them that the small size of the eye is diagnostic for +Xenocassis +and found that five species currently classified in the nominotypical subgenus should be transferred to +Xenocassis +based on this character. In addition we found that +Xenocassis +species are very variable regarding the size and presence of tarsal appendages. The genus was based by +Spaeth (1936) +on the outer claws of the metatarsi simple in both sexes, however, examination of extensive material revealed that even the type species, +Charidotella amoena +, could have the outer claws of the metatarsi with a large basal tooth. Similar situation was found in two other species we had extensive material to study - +Charidotella (Xenocassis) ambita +(Champion, 1894) and +Charidotella (Xenocassis) puella +(Boheman, 1855). In both the basal teeth showed variable size even within one population. While the size of the eye is constant. Some species of other subgenera have slightly smaller eyes than others thus they have gena visible but always very narrow while species of +Xenocassis +have gena covering approximately basal third of lateral side of the head. + + +We +consider +Xenocassis +as subgenus of +Charidotella +as the size of the eye is found variable also in some other new world +Cassidini +genera, e.g. +Charidotis +Boheman, 1855 and +Plagiometriona +Spaeth, 1899. + + +Last catalogue, +Borowiec (1999) +listed 10 species in the subgenus +Xenocassis +. We have recently examined types of all species and found that one was wrongly assigned to +Xenocassis +. +Coptocycla cingulata +Boheman, 1862 (type seen in the Natural History Museum, London) was unknown to most authors and have been tentatively placed in +Charidotella +based on the original description ( +Boheman 1862 +) and notes published by +Champion (1894) +in the +Cassidinae +volume of the Biologia Centrali Americana ( +Borowiec 1989 +). It posses all characters of the genus +Plagiometriona +and is here transferred to it as +Plagiometriona cingulata +(Boheman, 1862), comb. n. + + +During examination of species placed in the nominotypical subgenus we found four which had small eyes and are here transferred to +Xenocassis +: +Charidotella (Xenocassis) discoidalis +(Boheman, 1855), comb. n., +Charidotella (Xenocassis) incerta +(Boheman, 1855), comb. n., +Charidotella (Xenocassis) purpurea +(Linnaeus, 1758), comb. n., and +Charidotella (Xenocassis) myops +(Boheman, 1855), comb. n. Types of all, with exception of +Charidotella purpurea +, were examined and are preserved in the Naturhistoriska Riksmuseet, Stockholm, Sweden. In addition +Boheman (1855) +described two more species in the same groups as abovementioned ones and we have strong feeling that they belong to +Xenocassis +too: +Charidotella (Xenocassis) amoenula +(Boheman, 1855), comb. n. and +Charidotella (Xenocassis) cyclographa +(Boheman, 1855), comb. n. Unfortunately, we were not able to locate their type specimens thus the transfer is tentative, based on primary descriptions according to which the species should have the circular body shape, the annulus on upper side of the elytra, and coarser punctation on the lateral slope of elytral disc like other +Xenocassis +species. + + + + \ No newline at end of file diff --git a/data/38/1D/87/381D87A2FFC4FFCA7345FEEAFE50DE1A.xml b/data/38/1D/87/381D87A2FFC4FFCA7345FEEAFE50DE1A.xml new file mode 100644 index 00000000000..5421fc253a8 --- /dev/null +++ b/data/38/1D/87/381D87A2FFC4FFCA7345FEEAFE50DE1A.xml @@ -0,0 +1,88 @@ + + + +PachybrachisChevrolat (Coleoptera: Chrysomelidae: Cryptocephalinae) Endemic to Florida, Including Descriptions of Four New Species + + + +Author + +Barney, Robert J. + +text + + +The Coleopterists Bulletin + + +2016 + +2016-03-31 + + +70 + + +1 + + +31 +52 + + + + +http://dx.doi.org/10.1649/072.070.0104 + +journal article +10.1649/072.070.0104 +5341110 + + + + + + +Pachybrachis illectus + + + + +Specimens Examined. + +Holotype ++ +paratype +: + +USA +: +FLORIDA +: + +Volusia Co. +, +Enterprise +, 20.v, +Hubbard +& +Schwarz Collection +[ +1♂ +1♀ +, +1♂ +holotype +, +USNM +]. + + + + + +APPENDIX 4 + + + + \ No newline at end of file diff --git a/data/38/1D/87/381D87A2FFC7FFC97133FDF3FC51DF73.xml b/data/38/1D/87/381D87A2FFC7FFC97133FDF3FC51DF73.xml new file mode 100644 index 00000000000..6908354f4ff --- /dev/null +++ b/data/38/1D/87/381D87A2FFC7FFC97133FDF3FC51DF73.xml @@ -0,0 +1,102 @@ + + + +PachybrachisChevrolat (Coleoptera: Chrysomelidae: Cryptocephalinae) Endemic to Florida, Including Descriptions of Four New Species + + + +Author + +Barney, Robert J. + +text + + +The Coleopterists Bulletin + + +2016 + +2016-03-31 + + +70 + + +1 + + +31 +52 + + + + +http://dx.doi.org/10.1649/072.070.0104 + +journal article +10.1649/072.070.0104 +5341110 + + + + + + +Pachybrachis rileyi + + + + +Specimens Examined. + +Holotype ++ +20 paratypes +: + +USA +: +FLORIDA +: + +Monroe Co. +, +Upper Key Largo +, + +18.iii.1972 + +[ +1♀ +, +USNM +]; same data, except + +30.iv.1988 + +, mercury vapor & blacklight, +E. Riley +& +F. Whitford +[ +14♂♂ +5♀♀ +, +EGRC +; +1♂ +holotype +, +TAMU +]. + + + + + +APPENDIX 8 + + + + \ No newline at end of file diff --git a/data/38/1D/95/381D95F1C97BEAEC1090F47FD1DEC3A8.xml b/data/38/1D/95/381D95F1C97BEAEC1090F47FD1DEC3A8.xml new file mode 100644 index 00000000000..e03e8d3f23c --- /dev/null +++ b/data/38/1D/95/381D95F1C97BEAEC1090F47FD1DEC3A8.xml @@ -0,0 +1,71 @@ + + + +Checklist of British and Irish Hymenoptera - aculeates (Apoidea, Chrysidoidea and Vespoidea) + + + +Author + +Else, George R. + + + +Author + +Bolton, Barry + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8050 +8050 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8050 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8050 +1314-2828-4-8050 + + + + +Ponera testacea Emery, 1895 + + + + +crassisquama +Emery, 1916 + + + +Distribution +England + + +Notes + +added by +Attewell et al. (2010) + + + + \ No newline at end of file diff --git a/data/38/1D/A1/381DA1C9CCD0F627C374CFA903FA7F00.xml b/data/38/1D/A1/381DA1C9CCD0F627C374CFA903FA7F00.xml new file mode 100644 index 00000000000..57eafd64049 --- /dev/null +++ b/data/38/1D/A1/381DA1C9CCD0F627C374CFA903FA7F00.xml @@ -0,0 +1,74 @@ + + + +A snail in the long tail: a new Plekocheilus species collected by the ' Comision Cientifica del Pacifico' (Mollusca, Gastropoda, Amphibulimidae) + + + +Author + +Breure, Abraham S. H. + + + +Author + +Araujo, Rafael + +text + + +ZooKeys + + +2015 + +516 + + +85 +93 + + + + +http://dx.doi.org/10.3897/zookeys.516.10228 + +journal article +http://dx.doi.org/10.3897/zookeys.516.10228 +1313-2970-516-85 +D7838218FC5C49518F3752C854A24AA0 + + + +Taxon classification Animalia Stylommatophora Amphibulimidae + + + +Genus +Plekocheilus Guilding, 1828 + + + + +Plekocheilus +Guilding 1828 +: 532. + + + +Type species. + +Caprella undulata +Guilding, 1824, by monotypy. + + + + +Distribution +. + +West Indies, Panama, Colombia, Ecuador, Peru, Bolivia, Brazil, French Guyane, Suriname, Guyana, Venezuela. + + + \ No newline at end of file diff --git a/data/38/1D/CD/381DCDAF6BB5D2EC31D29F4FF5360C8F.xml b/data/38/1D/CD/381DCDAF6BB5D2EC31D29F4FF5360C8F.xml new file mode 100644 index 00000000000..67c4c5348c4 --- /dev/null +++ b/data/38/1D/CD/381DCDAF6BB5D2EC31D29F4FF5360C8F.xml @@ -0,0 +1,454 @@ + + + +Revision of Muhlenbergia (Poaceae, Chloridoideae, Cynodonteae, Muhlenbergiinae) in Peru: classification, phylogeny, and a new species, M. romaschenkoi + + + +Author + +Peterson, Paul M. + + + +Author + +Vega, Isidoro Sanchez + + + +Author + +Romaschenko, Konstantin + + + +Author + +Giraldo-Canas, Diego + + + +Author + +Rodriguez, Nancy F. Refulio + +text + + +PhytoKeys + + +2018 + +114 + + +123 +206 + + + + +http://dx.doi.org/10.3897/phytokeys.114.28799 + +journal article +http://dx.doi.org/10.3897/phytokeys.114.28799 +1314-2003-114-123 +CB70FFE82A46DE6DFFEBFFF8F43A6230 +2533527 + + + + +13 +. + +Muhlenbergia microsperma (DC.) Kunth, +Revis +. Gramin. 1:64. 1829. + +Fig. 7E-H + + + + +Trichochloa microsperma +DC., Cat. Pl. Horti Monsp. 151. 1813. +Muhlenbergia microsperma +(DC.) Trin., Gram. Unifl. Sesquifl. 193. 1824, +nom. inval +. Type: Mexico, cultivated at the botanical gardern at Montpellier from seeds collected in Mexico and distributed by the Botanical Garden of Madrid, + +M. +Sesse +& J.M. +Mocino +s.n. + +(holotype: MPU; isotypes: G-00099434 [image!], P!, US fragm. ex P!). + + +Agrostis microsperma +Lag., Gen. Sp. Pl. 2. 1816. Type: Mexico, plants grown at H.R. Matritensis (= Herbario del Real +Jardin +Botanico +de Madrid, see +Sutherland 1997 +) from seeds collected by M. +Sesse +& J.M. +Mocino +in Nueva Espania, Oct, 1806, + +M. +Sesse +& J.M. +Mocino +s.n. + +(lectotype, here designated: SEL-H10620 [image!]). + + +Podosemum debile +Kunth, Nov. Gen. Sp. (quarto ed.) 1: 128. 1816. +Trichochloa debilis +(Kunth) Roem. & Schult., Syst. Veg. 2:385. 1817. +Muhlenbergia debilis +(Kunth) Trin., Gram. Unifl. Sesquifl. 193, t. 5, f. 18. 1824. Type: Ecuador, Prov. Pichincha, Quito, +F.W.H.A. Humboldt & A.J.A. Bonpland s.n. +(holotype: P-Bonpl!; isotypes: B-W, P!, US-91924 fragm. ex P-Bonpl!). + + +Podosemum setosum +Kunth, Nov. Gen. Sp. (quarto ed.) 1:129. 1816. +Trichochloa setosa +(Kunth) Roem. & Schult., Syst. Veg. 2:386. 1817. +Agrostis setosa +(Kunth) Spreng., Syst. Veg. 1:262. 1825. +Muhlenbergia setosa +(Kunth) Trin., Gram. Unifl. Sesquifl. 193, t. 5, f. 22. 1824. +Muhlenbergia setosa +(Kunth) Kunth, +Revis +. Gramin. 1:63. 1829, +isonym +. Type: Mexico, between Gueguetoque and Tula, Aug, +F.W.H.A. Humboldt & A.J.A. Bonpland 4174 +(holotype: P-Bonpl!; isotypes: B-W, US-91917 fragm. ex P-Bonpl!). + + +Muhlenbergia purpurea +Nutt., J. Acad. Nat. Sci. Philadelphia, ser. 2, 1:186. 1848. Type: U.S.A., California, Santa Barbara Co., Santa Barbara and Santa Catalina Island, +Gambel s.n. +(holotype: K!). + + +Muhlenbergia ramosissima +Vasey, Bull. Torrey Bot. Club 13(12):231. 1886. Type: Mexico, Chihuahua, SW Chihuahua, +Aug-Nov +1885, +E. Palmer 158 +(lectotype: NY-00381467! designated by Hitchcock, N. Amer. Fl. 27:441. 1935, but without indicating the specific specimen; Peterson and Annable, Syst. Bot. Monogr. 31:61. 1991, indicated the specific specimen; isolectotypes: LE!, GH-00024043 [image!], MO-2974152!, NY-00381468 [image!], P-00644106!, PH-00018772 [image!], US-995580!, W-19160027660 [image!]). + + + +Description. + +Caespitose +annuals +, sometimes appearing as short-lived perennials. +Culms +10-80 cm tall, often geniculate at the base, slender, often striate, much branched near the base, scaberulous below the nodes; +internodes +1.8-8.6 mm long, mostly scaberulous or smooth. +Leaf sheaths +2.2-6.6 mm long, commonly shorter than the internodes, glabrous, smooth or scaberulous; +ligules +1-2 mm long, membranous to hyaline, decurrent, margins often extended, apex truncate to obtuse; +blades +3 +-8.5(- +10) cm long, 1-2.5 mm wide, flat or loosely involute, scabrous below, strigulose above, often deciduous with age. +Panicles +6.5-13.5 cm long, 1-6.5 cm wide, open and not densely flowered, often purplish; +primary branches +1.6-4 cm long, ascending or diverging up to 80° from the rachises, spikelet-bearing to the base; +pedicels +2-6 mm long, appressed to divaricate, antrorsely scabrous. + +Cleistogamous panicles + +with 1-3 spikelets present in the axils of the lower sheaths. +Spikelets +2.5-5.5 mm long; +glumes +0.4-1.3 mm long, exceeded by the florets, 1-nerved, obtuse, often minutely erose; +lower glumes +0.4-1 mm long; +upper glumes +0.6-1.3 mm long; +lemmas +2.5 +-3.8(- +5.3) mm long, narrowly lanceolate, mostly smooth, scaberulous distally, lower 1/2 of the margins and midveins, the hairs 0.2-0.5 mm long, the callus hairy, apices acuminate, often bidentate, awned, awns 10-30 mm long, straight to flexuous; +paleas +2.2-4.8 mm long, narrowly lanceolate, acuminate; +anthers +0.3-1.2 mm long, purplish. +Caryopses +1.7-2.5 mm long, fusiform, reddish-brown. 2 +n += 20, 40, 60. + + + +Distribution. + + +Muhlenbergia microsperma + +occurs in Hawaii, south-western U.S.A., Mexico, Guatemala, Colombia, Venezuela, Ecuador (including the Galapagos Islands), Peru and Bolivia ( +Peterson and Annable 1991 +). + + + +Ecology. + +Rocky slopes, rock outcrops, sandy drainages, cliffs and disturbed roadsides usually in desert scrub vegetation with + +Acacia +, +Aristida +adcensionis + +L., + +Baccharis + +, + +Bothriochloa + +, +Bombacaceae +, +Cactaceae +, + +Dodonaea viscosa + +, + +Eragrostis nigricans + +, + +E. lugens + +Nees, + +Fucraea + +, + +Heliotropium + +, + +Heteropogon contortus + +(L.) P. Beauv. ex Roem. & Schult., + +Lantana + +, + +Muhlenbergia rigida + +, + +Pitcairnia + +, + +Prosopis + +, + +Puya + +, + +Salvia + +, + +Schinus molle + +and + +Schizachyrium + +; 1150-3500 m. + + + +Comments. + + +Muhlenbergia microsperma + +can sometimes be confused with + +M. romaschenkoi + +and differs from it by having cleistogamous panicles in the axils of the lower sheaths and shorter, obtuse glumes, 0.4-1.3 mm long (glumes acute to acuminate, 2-2.8 mm long in + +M. romaschenkoi + +). + + +In a molecular DNA sequence study, + +M. microsperma + +forms a strongly supported clade with two other annuals, + +M. appressa + +C.O. Godding and + +M. brandegei + +C.G. Reeder, all members of +M. subg. Muhlenbergia +(Fig. +1B +; +Peterson et al. 2010b +). These three species produce cleistogamous spikelets in the axils of the lower culm branches, enclosed by a sheath ( +Peterson and Annable 1991 +). +Cleistogamous +spikelets appear to have evolved twice within + +Muhlenbergia + +, once in +M. subg. Muhlenbergia +within the + +M. appressa +- +M. brandegei +- +M. microsperma + +clade and once in +M. sect. Pseudosporobolus +in + +M. cuspidata + +(Torr. ex Hook.) Rydb. ( +Morden and Hatch 1984 +; +Peterson et al. 2010b +). + + + +Specimens examined. + +Peru. +Ancash +: at the Rio Yanamayo crossing, 57 km N of San Luis on road towards Pomabamba, 2540 m, 24 Mar 1997, P.M. Peterson & N. Refulio Rodriguez 13896 (US, USM); 68 km from Casma towards Huaraz, 1700 m, 4 Apr 1988, S.A. Renvoize & S. +Laegaard +5047 (CPUN, K); Pallasca, divide between Rio Conchucos and Rio Plata, low end of road up to Pampas from Rio Conchucos, above Mollapata crossing of Rio Tablachaca, +8°12'9.1"S +, +77°56'20.6"W +, 2233 m, 21 Mar 2008, P.M. Peterson & R.J. Soreng 21833 (MO, US, USM). +Apurimac +: Aymaraes, 16 km NW of Chalhuanca, +14°10'16.4"S +, +73°19'26.1"W +, 2670 m, 14 Mar 2002, P.M. Peterson & N. Refulio Rodriguez 16511 (US, USM); Chincheros, +canyon +of Rio Pampas, between Ayacucho and Abancay on hwy 7, 7 km S of bridge over Rio Pampas, +13°28'42.1"S +, +73°49'32"W +, 2049 m, 17 Mar 2007, P.M. Peterson, R.J. Soreng, K. Romaschenko & D. Susanibar Cruz 20535 (MO, US, USM). +Ayacucho +: alrededores de Huanta, 2400 m, 30 Apr 1964, O. Tovar 4829 (US, USM). +Cajamarca +: Cajabamba, WSW of Cajabamba, 14 air km E of Araqueda, +7°39'9.1"S +, +78°9'58.9"W +, 2242 m, 23 Mar 2008, P.M. Peterson & R.J. Soreng 21855 (US, USM); Cajamarca, Cerro Huacaris, valle de Cajamarca, 1 Jun 1971, I. +Sanchez +Vega 726, W. Ruiz Vigo & J. Tejada (CPUN); Cajamarca, abajo de San Juan, siguiendo la carretera +Cajamarca-Pacasmayo +, 1900 m, 18 May 1986, I. +Sanchez +Vega 4072 (CPUN); Cajamarca, entre San Juan y Magdalena, 1800 m, 15 May 1971, I. +Sanchez +Vega 657 & W. Ruiz Vigo (CPUN); entre Chancay y Valle de Condebamba, 2600 m, 6 May 1972, I. +Sanchez +Vega 944, W. Ruiz Vigo & M. Malpica R. (CPUN); Dist. +Ichocan +, en el Arboretum +Ichocan +II de CICAFOR, entre la localidad de Chacay y Valle Condebamba, 2450 m, 29 Mar 1981, I. +Sanchez +Vega 2409, V. Torrel & E. Medina (CPUN); Celendin, +Maranon +River Valley, Chachapoyas-Cajamarca road, 1900 m, 28 May 1984, D.N. Smith & J. Cabanillas 7254 (MO, US); Chota, Dist. Cochabamba, a 1km sobre la carretera +Cochabamba-Cutervo +, 1720 m, 15 Jun 1980, I. +Sanchez +Vega 2288 (CPUN). +Cusco +: Anta, Sisal, Limatambo, 2300 m, 15 Mar 1963, C. Vargas C. 14327 (US, USM); Anta, Sisal-Cunyaee, 2100 m, 14 May 1965, C. Vargas C. 16316 (US, USM). +Huancavelica +: Salcabamba-Colcabamba, camino a Pampas, 2000 m, 22 Apr 1962, O. Tovar 3834 (US, USM); Tayacaja, alrededores de Mayoc, 2400 m, 9 Apr 1966, O. Tovar 5589 (US, USM). + +Huanuco + +: +Huanuco +, W side of canyon of Rio Huallaga, S of Ambo, 7 km on hwy 3 towards Cerro de Pasco, +10°11'49"S +, +76°9'54"W +, 2345 m, 6 Mar 2007, P.M. Peterson, R.J. Soreng & K. Romaschenko 20326 (US, USM); +Huanuco +, 2125 M, 25 Apr 1923, J.F. Macbride 3514 (F, US); 5 Apr 1923, J.F. Macbride 3217 (F, US). +La Libertad +: Bolivar, 4.6 air km NW of Longotea, SE of San Vicente on road from Balsas to Longotea, +7°0'38"S +, +77°54'15.2"W +, 2058 m, 31 Mar 2008, P.M. Peterson, R.J. Soreng & J. Montoya Quino 21970 (MO, US, USM); Otuzco, Quirrpe-Membrillar, 1150 m, 7 Dec 1952, A. +Lopez +Miranda 927 (US); Santiago de Chuco, 22 km E of Huamachuco on road towards Sarin above Rio Chusgon, 2500 m, 29 Mar 1997, P.M. Peterson & N. Refulio Rodriguez 13973 (US, USM). +Lima +: Canta, 2 km SE of San Jose Canta, +11°30'2"S +, +76°40'23.4"W +, 2232 m, 27 Mar 2004, P.M. Peterson & N. Refulio Rodriguez 17985 (MO, US, USM); Huarochiri, Matucana, 2430 m, 12 Apr 1922, J.F. Macbride & Featherstone 392 (F, US); Huarochiri, km 70 carretera Lima-Oroya, 1800 m, 15 May 1963, R. Ferreyra 14892 (US, USM); km 68, cerca Surco, entre Chosica y Matucana, 1400 m, 27 Mar 1955, R. Ferreyra 10498 (US, USM); km 72 de la carretera Lima-Oroya, cerca de Surro, 1800 m, 14 May 1948, R. Ferreyra 3485 (MOL, US, USM); Prov. Lima, above Paya, E. Asplund 10825 (NY). +Piura +: Huancabamba, 10 km N of Sondor and 3 km S of Huancabamba, 1860 m, 1 Apr 2000, P.M. Peterson & N. Refulio Rodriguez 15167 (CPUN, MO, US, USM). +Tacna +: Zarata, Sitiqui, 3500 m, 7 Apr 1959, C. Vargas C. 12588 (US, USM). + + + + \ No newline at end of file diff --git a/data/38/1E/6B/381E6B372BB557C3AA0733202EF937D2.xml b/data/38/1E/6B/381E6B372BB557C3AA0733202EF937D2.xml new file mode 100644 index 00000000000..92fd3819d77 --- /dev/null +++ b/data/38/1E/6B/381E6B372BB557C3AA0733202EF937D2.xml @@ -0,0 +1,161 @@ + + + +The concluding chapter: recircumscription of Goodenia (Goodeniaceae) to include four allied genera with an updated infrageneric classification + + + +Author + +Shepherd, Kelly A. +Western Australian Herbarium, Department of Biodiversity, Conservation & Attractions, Kensington, WA 6151, Australia +https://orcid.org/0000-0003-1627-7891 +kelly.shepherd@dbca.wa.gov.au + + + +Author + +Lepschi, Brendan J. +Australian National Herbarium, Centre for Australian National Biodiversity Research, GPO Box 1700, Canberra, ACT, 2601, Australia + + + +Author + +Johnson, Eden A. +Department of Biology, University of Mississippi, Oxford, MS 38677, USA + + + +Author + +Gardner, Andrew G. +Department of Biological Sciences, California State University, Stanislaus, Turlock, CA 95382, USA + + + +Author + +Sessa, Emily B. +Department of Biology, University of Florida, Gainesville, FL 32607, USA + + + +Author + +Jabaily, Rachel S. +Department of Organismal Biology & Ecology, Colorado College, Colorado Springs, CO 80903, USA + +text + + +PhytoKeys + + +2020 + +152 + + +27 +104 + + + + +http://dx.doi.org/10.3897/phytokeys.152.49604 + +journal article +http://dx.doi.org/10.3897/phytokeys.152.49604 +1314-2003-152-27 +9E670F26B4635D2FA9E36777E3C2DD70 + + + + +Goodenia subg. Monochila sect. Scaevolina (Carolin) K.A.Sheph., comb. et +stat. nov. + + + + +≡ +Goodenia subsect. Scaevolina +Carolin in A.S.George (ed.), Fl. Austral. 35: 331. 1992 - Type: +G. scaevolina +F.Muell. + + + +Description. + +Subshrubs +or +herbs +. +Leaves +basal or cauline, basal leaves sometimes absent in mature plants. +Flowers +in thyrses or racemes comprising at least 1/2 to 2/3 of the plant, with leafy bracts; bracteoles present. +Sepals +equal. +Corolla +bilabiate or becoming fan-like, blue usually with a yellow or whitish throat, usually with hairs on margins and in the throat, enations prominent; scarcely auriculate; pouch usually prominent. +Ovary +2-locular with 20-60 ovules in two rows in each locule. +Fruit +a capsule, valves entire or bifid. +Seeds +> 1.5 mm wide, wing +c. +0.1 mm wide and mucilaginous or obsolete. + + + +Number of taxa and distribution. +A section of eight species from northern and central Australia extending southwards into the Eremaean bioregion of Western Australia. + + +Included species. + + +G. azurea + +F.Muell., +Goodenia azurea F.Muell. subsp. azurea +, +G. azurea subsp. hesperia +L.W.Sage & Albr., + +G. eremophila + +E.Pritz., + +G. hartiana + +L.W.Sage, + +G. ramelii + +F.Muell., + +G. scaevolina + +F.Muell., + +G. splendida + +A.E.Holland & T.P.Boyle, + +G. stobbsiana + +F.Muell., + +G. suffrutescens + +Carolin. + + + + \ No newline at end of file diff --git a/data/38/1E/71/381E7195919DFA56CCB04B7BF1BF8FC9.xml b/data/38/1E/71/381E7195919DFA56CCB04B7BF1BF8FC9.xml new file mode 100644 index 00000000000..b34850f2955 --- /dev/null +++ b/data/38/1E/71/381E7195919DFA56CCB04B7BF1BF8FC9.xml @@ -0,0 +1,51 @@ + + + +A synoptic review of the ants of California (Hymenoptera: Formicidae). + + + +Author + +Ward, P. S. + +text + + +Zootaxa + + +2005 + +936 + + +1 +68 + + + + +http://antbase.org/ants/publications/21008/21008.pdf + +journal article +21008 + + + + + + +Neivamyrmex minor (Cresson +1872) + + + + + +Species is known from males only. + + + + + \ No newline at end of file diff --git a/data/38/1E/7C/381E7C1B94E2B016F7CDA11FBCA7E589.xml b/data/38/1E/7C/381E7C1B94E2B016F7CDA11FBCA7E589.xml new file mode 100644 index 00000000000..de2281a3da5 --- /dev/null +++ b/data/38/1E/7C/381E7C1B94E2B016F7CDA11FBCA7E589.xml @@ -0,0 +1,65 @@ + + + +Brazilian Trichoptera Checklist II + + + +Author + +Paprocki, Henrique + + + +Author + +Franca, Diogo + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1557 +1557 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1557 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1557 +1314-2828--1557 + + + + + +Nectopsyche gemma ( +Mueller +), 1880 + + + + +Distribution +Santa Catarina + + +Notes + + +Mueller +1880 + + + + + \ No newline at end of file diff --git a/data/38/1E/E8/381EE8B6829C86F102165FCF6464ABAE.xml b/data/38/1E/E8/381EE8B6829C86F102165FCF6464ABAE.xml new file mode 100644 index 00000000000..54c4c303f41 --- /dev/null +++ b/data/38/1E/E8/381EE8B6829C86F102165FCF6464ABAE.xml @@ -0,0 +1,117 @@ + + + +Family-group names in Coleoptera (Insecta) + + + +Author + +Bouchard, Patrice + + + +Author + +Bousquet, Yves + + + +Author + +Davies, Anthony E. + + + +Author + +Alonso-Zarazaga, Miguel A. + + + +Author + +Lawrence, John F. + + + +Author + +Lyal, Chris H. C. + + + +Author + +Newton, Alfred F. + + + +Author + +Reid, Chris A. M. + + + +Author + +Schmitt, Michael + + + +Author + +Ślipinski, S. Adam + + + +Author + +Smith, Andrew B. T. + +text + + +ZooKeys + + +2011 + +88 + + +1 +972 + + + + +http://dx.doi.org/10.3897/zookeys.88.807 + +journal article +http://dx.doi.org/10.3897/zookeys.88.807 +1313-2970-88-1 + + + + +Subtribe +Aleocharina Fleming, 1821 + + + + +Aleocharidae +Fleming, 1821: 49 [stem: Aleochar-]. Type genus: +Aleochara +Gravenhorst, 1802. + + +Piochardiae +Fenyes, 1918: 20 [stem: Piochardi-]. Type genus: +Piochardia +Heyden, 1870. + + + + \ No newline at end of file diff --git a/data/38/1F/23/381F236E1ED1A2AD37158240A90E756D.xml b/data/38/1F/23/381F236E1ED1A2AD37158240A90E756D.xml new file mode 100644 index 00000000000..0e43053b7d1 --- /dev/null +++ b/data/38/1F/23/381F236E1ED1A2AD37158240A90E756D.xml @@ -0,0 +1,280 @@ + + + +Trigonalidae (Hymenoptera) from cacao agroforestry systems in northeastern Brazil, with two new species of Trigonalys Westwood + + + +Author + +Santos, Bernardo F. +Universidade Federal do Espirito Santo, Depto de Ciencias Biologicas, Av. Fernando Ferrari, s / n - Goiabeiras, Vitoria, ES, 29075 - 010, Brazil + + + +Author + +Aguiar, Alexandre P. + + + +Author + +Tedesco, Anazelia M. + +text + + +Journal of Hymenoptera Research + + +2012 + +2012-03-23 + + +25 + + +19 +34 + + + + +http://dx.doi.org/10.3897/jhr.25.1810 + +journal article +http://dx.doi.org/10.3897/jhr.25.1810 +1314-2607-25-19 +55222C6B934840E1A49504653889F633 +FFE04F584B2C3221FFFFFF90FF9F0679 +574774 + + + + +Trigonalys erythrocephala Santos & Aguiar +sp. n. +Figs 3-12 + + + +Holotype + +♀, Brazil, Bahia, +Urucuca +, Fazenda Bom Jardim, Pt 5, 25.XI.2002, Malaise trap, J. Cardoso & J. Maia (UFES). Mounted on a triangle point; in good condition. + + + +Paratype +♀, same data as holotype, except Pt 7, 23.XI.2002 (CEPLAC). + + +Diagnosis. +Frons, most of vertex, and temple, reddish brown; metasomal armature of sternum III conspicuous, Y-shaped; supra-antennal elevation stout, conspicuous; hind coxa dorsally somewhat concave longitudinally, forming two longitudinal edges on each side, throughout its length, dorso-mesal portion strigate; legs entirely dark brown; fore wing nearly uniformly infuscate, except slightly darker along anterior margin. + + +Description. +Holotype: body length 8.5 mm; fore wing length 7.4 mm. + +Head +( +Figs 1, 2 +- +4 +). Mandible covered with long and moderately dense setae; ventral tooth of right mandible distinctly longest and narrowest, median teeth length subequal, [dorsal tooth not visible; mandibles closed, left mandible not observed]. +Clypeus +2.28 +x +as wide as maximum length, laterally distinctly pilose, centrally glabrous, faintly punctate. Inner margin of eyes subparallel; interocular distance at narrowest level 1.17 +x +maximum eye height. Antenna with 25 flagellomeres, about 1.4 +x +the lateral length of mesosoma; intertoruli distance slightly longer than distance from torulus to inner margin of eye. Supra-antennal elevation conspicuous, laterally a sharp carina ( +Fig. 5 +), between antennae with rounded border. Frons pilose, densely punctate; punctation at median portion dorsally sparse, feeble; frons medially with a subtle longitudinal depression; area around and between ocelli slightly concave ( +Fig. 5 +). Vertex shiny, densely pilose, moderately punctate. Gena maximum width in lateral view 0.83 +x +maximum eye height, finely punctate, densely pilose, particularly at ventral 0.4. Occipital carina conspicuous, widest dorsally, narrowest ventrally. + + +Mesosoma +( +Figs 3, 7-8 +). Densely pilose. Pronotum: anterior, neck-shaped portion moderately long, laterally transversally wrinkled ( +Fig. 3 +), centrally distinctly concave, anterior margin wide, polished; pronotum lateral area dorsally densely punctate, ventrally sparsely punctate, its posterior margin with distinct longitudinal wrinkles; central portion of lateral area intensely concave, anteriorly with stout oblique carina ( +Fig. 10 +). Mesoscutum and scutellum deeply punctate ( +Fig. 7 +), almost punctate-reticulate; notaulus deeply impressed, with distinct transverse wrinkles inside; median lobe of mesoscutum progressively raised from lateral lobes, until quite detached at anterior end; median lobe and scutellum with shallow but distinct mid-longitudinal sulcus; scutellum anteriorly with distinct longitudinal crenulation, centrally distinctly projected, subpyramidal; posterior margin shiny and impunctate. Hypoepimeron distinctly projected, subpyramidal, punctate, except small posterior area shiny and impunctate; scrobal sulcus distinct, somewhat crenulate; mesopleuron otherwise mostly punctate to areolate-punctate. Mesopleural suture dorsally deeply carinate. Metanotum (a narrow yellow stripe; +Fig. 7 +) anteriorly moderately punctate, posteriorly impunctate; metapostnotum (the subsequent black stripe) rugose. Metapleuron finely punctate. Transverse sulcus at base of propodeum as long as metapostnotum, shallow, finely crenulate ( +Fig. 8 +). Propodeum densely pilose, laterally setae distinctly longer than centrally; antero-lateral corners longitudinally rugose, otherwise mostly punctate-areolate or areolate-rugose, centrally and posteriorly in concentric patterns, anteriorly with shiny and almost impunctate area; propodeal spiracle covered by prominent, tubercle-like flap. Propodeal foramen somewhat M-shaped ( +Fig. 8 +). Hind coxa with two sharp lateral angles extending throughout its length ( +Fig. 11 +), dorso-mesal portion strigate. + + +Wings +. Fore wing vein M arising almost opposite to crossvein 1cu-a; crossvein 2m-cu distinctly sinuous, with bulla on anterior 0.75; crossveins 2r-m and 3r-m almost straight. Second submarginal cell distinctly petiolate; third submarginal cell subtrapezoidal, slightly wider than high. + + +Metasoma +. Densely covered with short setae. Tergum I slightly concave, short and broad, trapezoidal in dorsal view; 0.45 +x +as long as maximum width, apical widt +h +1.48 +x +basal width; mid-basally with a few distinct, somewhat concentric rugulosities; posterior margin nearly straight across, with large but shallow punctures. Terga II-V and sterna I-V densely punctate, densely covered with short setae. Metasomal armature developed on sternum III as single, Y-shaped, very sclerotinized projection, with pointed corners ( +Fig. 9 +). Ovipositor sheath shaped as a curved beak, laterally with longitudinal carina ( +Fig. 9 +). + + +Color +. Head mostly reddish brown, body mostly black, with yellowish marks. Head: antenna basally ferruginous, otherwise brown or nearly so; palpi dark brown; ventral margin of mandible, teeth apex, clypeal borders, small marks dorsad to toruli, subtriangular mark on vertex and most of gena and occiput, black; mandible except apex, clypeus, area around ventral 0.7 of eye and small marks on gena and around subtriangular black area, pale yellow; subapical portion of mandible between yellow and black areas, frons, most of vertex, and area around dorsal 0.3 of eye, reddish brown; vertex with dark, triangular mark behind ocelli, extending and narrowing posteriorly until it reaches occipital carina; a yellow stripe along each side of dark triangle. Mesosoma: black, except pale yellow to yellow on pronotal collar, dorsal margin of pronotum, margins of median mesoscutal lobe, alongside notaulus, lateral longitudinal marks on scutellum, axilla, metanotum, small central spot on mesopleuron, on apex of pyramidal projection, and J-shaped mark on each side of propodeum. Prominence of propodeal spiracle ferruginous. Legs apically to coxae dark brown. Wings slightly infuscate, fore wing darker towards anterior margin. Metasoma: black; all terga and sterna with posterior pale yellow stripes, on terga II-V also extending laterally; tergum VI brownish; sternum V almost entirely pale yellow. + + +Male. +Unknown. + + + +Variation. + +Holotype with terga II-IV showing anomalous development ( +Fig. 12 +). Paratype body length 9.3 mm; fore wing length 7.7 mm; yellow marks on gena and near subtriangular black mark at vertex, very subtle; propodeum anteriorly more distinctly sculptured, without shiny and almost impunctate area; propodeal foramen U-shaped; second submarginal cell less distinctly petiolate. + + + +Comments. + +In terms of general morphology, this species is closest to + +Trigonalys melanoleuca + +, from which it can be readily differentiated by its color pattern, with frons, most of vertex, and part of gena, reddish brown (vs. black with whitish marks, without reddish brown areas in + +Trigonalys melanoleuca + +); yellow marks at pronotal collar, dorsal margin of pronotum, mesoscutum, scutellum, and metanotum (vs. marks absent); yellow mark at mesopleuron very small and placed dorsad to longitudinal sulcus (vs. large, placed ventrad to sulcus); legs entirely dark brown (vs. with extensive white marks); and yellow marks on propodeum and metasoma less extensive than in + +Trigonalys melanoleuca + +. Additionally, + +Trigonalys melanoleuca + +has the fore wing more distinctly infuscated, metasomal armature absent, posterior margin of tergum I rounded (vs. nearly straight), propodeum uniformly punctate (vs. laterally areolate, anteriorly coriarious and posteriorly striate) and propodeal foramen always shaped as an inverted U (vs. U- or M-shaped). + + +The color pattern of + +Trigonalys erythrocephala + +is more similar to that of + +Trigonalys gotica + +, which is also mostly blackish with yellow marks on the pronotal collar, dorsal margin of +pronotum +, mesoscutum, scutellum, and metanotum. However, the two species differ markedly in general structure. + +Trigonalys gotica + +has a subtle supra-antennal elevation (vs. stout, conspicuous in + +Trigonalys erythrocephala + +); vertex deeply punctate-areolate (vs. moderately punctate); pronotal collar very slightly raised (vs. moderately raised), pronotum with a less evident oblique carina; hind coxa laterally with slight, blunt angles and without strigate area; propodeal foramen V-shaped (vs. U- or M-shaped), and female armature absent (vs. well developed). + + + +Trigonalys erythrocephala + +can be differentiated from + +Trigonalys sanctaecatharinae + +mainlyby the distinct, Y-shaped female armature (vs. delicate, not distinctly Y-shaped) and by the quite different color pattern ( +Figs 3 +, +20 +). + + +It can also be distinguished from the other New World species of + +Trigonalys + +as follows. Both + +Trigonalys flavescens + +Bischoff and + +Trigonalys maculifrons + +Sharp have an elongate body, resembling species of + +Orthogonalys + +Schulz. Both are also mostly yellow or orange with black marks, including the head yellow with black marks on frons (vs. reddish, without black marks at frons); scutellum yellow with posterior black mark (vs black with sublateral, narrow yellowish lines) and legs mostly yellow (vs. black and dark brown); basal third of tergum I dark brown and remainder yellow (vs. tergum I basal 0.7-0.8 black, apically yellowish). + +Trigonalys championi + +Cameron, has the antenna entirely black (vs ferruginous to brown); frons, vertex and gena black (vs. mostly reddish); fore wing entirely violaceous (vs. slightly infuscate, darker at anterior margin); propodeum and petiole mostly whitish (vs. propodeum black with sublateral narrow yellowish marks, petiole mostly black with apical 0.2-0.3 yellowish); and other metasomal segments entirely black (vs. with extensive yellowish marks). + + +Etymology +. From the Greek +erythros +, red, and +cephalon +, head, in reference to the somewhat characteristic color of the head capsule. + + + +Figures 3-12. + +Trigonalys erythrocephala + +Santos et Aguiar, +sp +. +n. +Holotype female. +3 +Lateral habitus (Morphobank accession number M90448) +4 +Head, antero-ventral (M90449) +5 +Head, antero-dorsal, to show ocelli (M90450) +6 +Head, dorsal (M90451) +7 +Mesothorax, dorsal (M90452) +8 +Propodeum and base of petiole, dorsal (M90453) +9 +Apical segments of metasoma, latero-ventral, left, showing metasomal armature and ovipositor; arrow indicates position of longitudinal carina (M90454) +10 +Pronotum, left (M90455) +11 +Left hind coxa, to show lateral longitudinal carinae (arrows) and dorso-mesal strigation (M90456) +12 +Apical tergites, to show abnormal development of tergites (M90457). + + + + + \ No newline at end of file diff --git a/data/38/1F/25/381F25B1D3CB5134A34D478BF2B657FB.xml b/data/38/1F/25/381F25B1D3CB5134A34D478BF2B657FB.xml new file mode 100644 index 00000000000..8553d6ce2ad --- /dev/null +++ b/data/38/1F/25/381F25B1D3CB5134A34D478BF2B657FB.xml @@ -0,0 +1,60 @@ + + + +Species plantarum: exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas + + + +Author + +Linnaeus, Carolus + +text + +1753 +Laurentius Salvius + +Stockholm + + + +https://doi.org/10.5962/bhl.title.669 + +book +10.5281/zenodo.3931989 +3931989 + + + + +Heracleum panaces +, +spec. nov. + + + + +3. Heracleum foliis pinnatis; foliolis quinis: intermediis sessilibus, floribus radiatis. +Hort. ups. 65. +* + + +Heracleum foliolis palmatis serratis. +Hort. cliff. 103. Roy. lugdb. 113. + + +Panax sphondylii folio s. Heracleum. +Bauh. pin. 157. + + + + +Habitat in +Apenninis +, +Sibiria +. ♂ + + + + \ No newline at end of file diff --git a/data/38/1F/5A/381F5A7118CB54ED80A903EEF9D0F6B6.xml b/data/38/1F/5A/381F5A7118CB54ED80A903EEF9D0F6B6.xml new file mode 100644 index 00000000000..7b16eb93807 --- /dev/null +++ b/data/38/1F/5A/381F5A7118CB54ED80A903EEF9D0F6B6.xml @@ -0,0 +1,122 @@ + + + +Distribution of wild bee (Hymenoptera: Anthophila) and hoverfly (Diptera: Syrphidae) communities within farms undergoing ecological transition + + + +Author + +Noel, Gregoire +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium +gregoire.noel@uliege.be + + + +Author + +Bonnet, Julie +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + + + +Author + +Everaerts, Sylvain +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + + + +Author + +Danel, Anouk +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + + + +Author + +Calderan, Alix +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + + + +Author + +de Liedekerke, Alexis +Ferme de Froidefontaine, Havelange, Belgium + + + +Author + +de Montpellier d'Annevoie, Clotilde +Department of Geography, Institute Transitions, University of Namur, Namur, Belgium & Ferme d'Emeville, Havelange, Belgium + + + +Author + +Francis, Frederic +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + + + +Author + +Serteyn, Laurent +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + +text + + +Biodiversity Data Journal + + +2021 + +2021-01-14 + + +9 + + +60665 +60665 + + + + +http://dx.doi.org/10.3897/BDJ.9.e60665 + +journal article +http://dx.doi.org/10.3897/BDJ.9.e60665 +1314-2828-9-e60665 +A14A82B6E4E456E6AA051CADA0ECE3E6 + + + + +Andrena (Melandrena) nigroaenea (Kirby 1802) + + + +Ecological interactions + + +Feeds on +Polylectic + + +Conservation status +Least Concern + + +Notes + +Table +2 + + + + \ No newline at end of file diff --git a/data/38/1F/D3/381FD35136EE8F7C7BB159F516FB67FE.xml b/data/38/1F/D3/381FD35136EE8F7C7BB159F516FB67FE.xml new file mode 100644 index 00000000000..9cdd08736d1 --- /dev/null +++ b/data/38/1F/D3/381FD35136EE8F7C7BB159F516FB67FE.xml @@ -0,0 +1,115 @@ + + + +Order Carnivora + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +532 +628 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Catopuma temminckii +subsp. +temminckii +Vigors and Horsfield 1827 + + + + + + + +Catopuma temminckii +subsp. +temminckii +Vigors and Horsfield 1827 + +, +Zool. J., 3: 451 + +. + + + + +Type Locality: + +" +Sumatra +" [ +Indonesia +]. + + + + + +Synonyms: + +Catopuma temminckii +subsp. +aurata +(Blyth 1863) + +; + +Catopuma temminckii +subsp. +bainsei +(Sowerby 1924) + +; + +Catopuma temminckii +subsp. +moormensis +( +Hodgson 1831 +) + +; + +Catopuma temminckii +subsp. +nigrescens +(Gray 1863) + +. + + + + \ No newline at end of file diff --git a/data/38/20/6A/38206A2E0EF72EE6A8D6247A03F3C6E2.xml b/data/38/20/6A/38206A2E0EF72EE6A8D6247A03F3C6E2.xml new file mode 100644 index 00000000000..fc2b6a4dca8 --- /dev/null +++ b/data/38/20/6A/38206A2E0EF72EE6A8D6247A03F3C6E2.xml @@ -0,0 +1,186 @@ + + + +Three new species of Fufius Simon, 1888 (Araneae, Cyrtaucheniidae) from Brazil with the redescription of Fufius funebris Vellard, 1924 and description of the female of Fufius lucasae Guadanucci & Indicatti, 2004 + + + +Author + +Ortega, Diego Ribeiro Migueis + + + +Author + +Nagahama, Roberto Hiroaki + + + +Author + +Motta, Paulo Cesar + + + +Author + +Bertani, Rogerio + +text + + +ZooKeys + + +2013 + +352 + + +93 +116 + + + + +http://dx.doi.org/10.3897/zookeys.352.6189 + +journal article +http://dx.doi.org/10.3897/zookeys.352.6189 +1313-2970-352-93 +42613A9C05FE444FA07021BF169F034B + + + + + +Fufius +minusculus + +sp. n. +Figs 27-36, 45 + + + +Diagnosis. +Male and female differ from those of all other species by carapace at least 1.5 times longer than wide and small sternal sigillae (Figs 32-36). + + +Etymology. +The specific name refers to the tiny size of the species. + + +Types. + +Holotype male from Brazil, Tocantins, Mateiros, +Jalapao +[ +10°32'S +, +46°24'W +], 01 November 2004, S. Balbino, with pitfall trap (DZUB 3416). Paratype: female from Brazil, Tocantins, Palmas, km 1.5 on the railway TO-010 (Palmas-Lajeado) [ +10°09'S +, +48°18'W +], 3 November 2001, I. Knysak & R. Martins (IBSP 9695). + + + +Additional material examined. + +BRAZIL: Tocantins: Palmas [ +10°10'S +, +48°19'W +], 2 immatures, 30 September 2001, I. Knysak & R. Martins (IBSP 9689). + + + +Male description + +(DZUB 3416). Total length: 5.11. Carapace 2.42 long, 1.60 wide, chelicerae 1.09 long, 0.60 wide. Palp: femur 1.24/ patella 0.66/ tibia 0.86/ tarsus 0.46/ total 3.22. Legs (femur, patella, tibia, metatarsus, tarsus, total): I: 1.88, 1.07, 1.39, 1.41, 0.95, 6.70. II: 1.61, 0.93, 1.31, 1.30, 0.97, 6.12. III: 1.14, 0.78, 0.70, 0.98, 0.35, 3.95. Leg IV missing. Mid-widths (lateral): femora +I-III += 0.40, 0.38, 0.51, palp = 0.31; patellae +I-III += 0.38, 0.32, 0.38, palp = 0.34; tibiae +I-III += 0.49, 0.23, 0.30, palp = 0.44; metatarsi +I-III += 0.27, 0.19, 0.18; tarsi +I-III += 0.21, 0.13, 0.18, palp = 0.26. Abdomen 2.41 long, 1.29 wide. Spinnerets: PMS, 0.25 long, 0.15 wide, 0.13 apart; PLS, 0.34 basal, 0.22 middle, 0.28 distal; mid-widths (lateral), 0.26, 0.20, 0.15, respectively. Carapace (Fig. 35): length to width 1.51. Fovea slightly recurved, 0.37 wide. Eyes: tubercle 0.19 high, length 0.32, width 0.50. Clypeus 0.02. Anterior and posterior eye row recurved. Eyes sizes and inter-distances: AME 0.14, ALE 0.14, PME 0.05, PLE 0.11, +AME-AME +0.05, +AME-ALE +0.04, +PME-PME +0.23, +PME-PLE +0.02, +ALE-PLE +0.03, +AME-PME +0.05, +ALE-ALE +0.34, +PLE-PLE +0.31. Eye group width 0.54, length 0.26. Maxillae (Fig. 36) 0.59 long, 0.80 wide. Cuspules: 12 spread over ventral inner heel. Labium: 0.31 long, 0.52 wide, with 2 cuspules. Labio-sternal groove shallow, flat, sigillae not evident. Sternum: 1.44 long, 1.13 wide. Sigillae: first, second pairs small, rounded, less than one diameter from margin. Third small, oval, one diameter from margin. Chelicerae: basal segment with 6 teeth. Legs: leg formula: I II III (legs IV missing). Scopula: tarsi +I-II +scopulate. Metatarsi III ascopulate (leg IV missing). Spines: palp: femur p-0-0-1, patella 0, tibia 0; leg I: femur d1-0-0, patella 0, tibia v1-1-0, metatarsus v0-0-ap1, p0-0-ap1; leg II: femur d 1-0-0, patella 0, tibia v 1-1-1ap, metatarsus v1-1-1ap; leg III: femur v1-0-0, patella p4, tibia d1-0-1, r0-0-1ap, v0-1-2ap, p0-0-1ap, metatarsus d1-3-2(1ap), r0-0-1ap, v1-2-2ap, p0-1-1. Leg IV missing. ITC smooth, STC with two rows of 5-8 teeth on both margins on all legs. Palp (Figs 27-28): embolus 0.46 in length. Embolus basal, middle, distal width of 0.22, 0.02, 0.01, respectively. Tegulum 0.24 long. Tibial spur (29-31) formed by single branch 0.28 long, 0.22 wide, on retrolateral margin, with apical spine. Color pattern: carapace, chelicerae reddish brown, darker on cephalic area, carapace margin, chelicerae; sternum, labium, maxillae, coxae of legs and palp light brown; abdomen +dark +with light brown punctuations on dorsum, larger white spot on central anterior area. Ventrally dark with central area whitish. Spinnerets light brown with dark brown setae. Legs yellowish with black areas on distal femora, most of patellae, tibiae, metatarsi. + + + +Figures 27-31. +Fufius minusculus +sp. n., holotype male 27-28 left palpal bulb 27 prolateral view 28 retrolateral view 29-31 right leg I tibial spur 29 ventral view 30 prolateral view 31 retrolateral view. Scale bar = 1mm. + + + + +Figures 32-36. +Fufius minusculus +sp. n. 32-34 paratype female 32 carapace 33 sternum, labium and maxillae 34 spermathecae, dorsal view 35-36 holotype male 35 carapace 36 sternum, labium, and maxillae. Scale bar = 1mm. + + + + +Female description + +(IBSP 9695). Total length: 5.19. Carapace 3.16 long, 2.18 wide, chelicerae 0.93 long, 0.75 wide. Palp: femur 1.58, patella 0.98, tibia 0.68, tarsus 0.93, total 4.17. Legs (femur, patella, tibia, metatarsus, tarsus, total): I: 1.79, 1.15, 1.20, 1.06, 0.77, 5.97. II: 1.32, 0.88, 0.85, 0.98, 0.98, 5.01. III: 1.35, 0.92, 0.64, 0.89, 0.88, 4.68. IV: 1.69, 1.09, 1.56, 1.41, 0.76, 6.51. Mid-widths (lateral): femora +I-IV += 0.48, 0.51, 0.56, 0.51, palp = 0.40; patellae +I-IV += 0.46, 0.46, 0.45, 0.43, palp = 0.38; tibiae +I-IV += 0.44, 0.33, 0.37, 0.38, palp = 0.38; metatarsi +I-IV += 0.27, 0.21, 0.23, 0.24; tarsi +I-IV += 0.26, 0.22, 0.17, 0.22, palp = 0.29. Abdomen 3.36 long, 2.40 wide. Spinnerets: PMS, 0.40 long, 0.23 wide, 0.35 apart; PLS, 0.65 basal, 0.51 middle, 0.49 distal; mid-widths (lateral), 0.34, 0.28, 0.26, respectively. Carapace (Fig. 32): length to width 1.45. Fovea slightly recurved, 0.45 wide. Eyes: tubercle 0.15 high, length 0.46, width 0.62. Clypeus 0.07. Anterior and posterior eye row recurved. Eyes sizes and inter-distances: AME 0.17, ALE 0.18, PME 0.08, PLE 0.11, AME 0.05, +AME-ALE +0.04, +PME-PME +0.27, +PME-PLE +0.03, +ALE-PLE +0.03, +AME-PME +0.07, +ALE-ALE +0.45, +PLE-PLE +0.40. Eye group width 0.63, length 0.29. Maxillae (Fig. 33) 0.72 long, 0.93 wide. Cuspules: ca. 30 spread over ventral inner heel. Labium: 0.45 long, 0.55 wide, with 2 cuspules. Labio-sternal groove shallow, flat, sigillae not evident. Sternum: 1.60 long, 1.23 wide. Sigillae: first, second pairs small, rounded, less than one diameter from margin. Third small, oval, one diameter from margin. Chelicerae: basal segment with 7 teeth. Legs: leg formula: IV I II III. Scopula: tarsi +I-II +scopulate. Metatarsi I 1/3 scopulate. Spines: palp: femur 0, patellae r1-1-0, tibia v2-2-3ap, r1-1-1ap, p0-0-1, tarsus v2-0-0; leg I: femur p0-0-1ap, patellae p0-0-1ap, tibia v1-1-1ap, metatarsus v1-1-2ap; leg II: femur 0, patellae r1-1-0, tibia v1-1-2, metatarsus v0-3-3(2ap), p0-1-0, r0-0-1; leg III: femur 0, patellae p4, r1, tibia d1-0-0, r0-1-0, v0-2-2ap, p1-1-0, metatarsus d1-3-2ap, r0-0-1, v0-4-2ap, p0-1-0; leg IV: femur 0, patella 0, tibia v0-1-2, r0-1-1, metatarsus d0-0-1ap, r0-1-0, v0-2-1ap, p1-1-1ap. Preening-comb: absent on retrolateral tip of metatarsus IV. Palp with single claw having 8 small teeth on internal margin. ITC smooth, STC with two rows of 5-9 teeth on both margins on all legs. Spermathecae (Fig. 34): two spermathecae having narrow and inward curved stalk, giving origin to two sinuous branches ending in single bulb each. Color pattern: as in male. + + + +Distribution. +Brazil, state of Tocantins (Palmas and Mateiros) (Fig. 45). + + + \ No newline at end of file diff --git a/data/38/20/B1/3820B1F1D8AF2A4B4D56963C7333E354.xml b/data/38/20/B1/3820B1F1D8AF2A4B4D56963C7333E354.xml new file mode 100644 index 00000000000..f67da33688b --- /dev/null +++ b/data/38/20/B1/3820B1F1D8AF2A4B4D56963C7333E354.xml @@ -0,0 +1,148 @@ + + + +Ninety-eight new species of Trigonopterus weevils from Sundaland and the Lesser Sunda Islands + + + +Author + +Riedel, Alexander + + + +Author + +Taenzler, Rene + + + +Author + +Balke, Michael + + + +Author + +Rahmadi, Cahyo + + + +Author + +Suhardjono, Yayuk R. + +text + + +ZooKeys + + +2014 + +467 + + +1 +162 + + + + +http://dx.doi.org/10.3897/zookeys.467.8206 + +journal article +http://dx.doi.org/10.3897/zookeys.467.8206 +1313-2970-467-1 +319040F01D0F495092BFA2FF705517AF +319040F01D0F495092BFA2FF705517AF + + + +Taxon classification Animalia Coleoptera Curculionidae + + + +89. +Trigonopterus suturalis Riedel +sp. n. + + + +Diagnostic description. + +Holotype, male (Fig. 89a). Length 2.53 mm. Color of head, legs, and sutural interval of elytra ferruginous, remainder black. Body in dorsal aspect with marked constriction between pronotum and elytron; with distinct constriction in profile. Rostrum with median ridge and pair of submedian ridges, intervening furrows punctate; epistome with indistinct, transverse, subangulate ridge. Pronotum anterolaterally angularly projecting; with distinct subapical constriction; disk punctate, interspaces microreticulate; punctures each with one slender suberect scale; with median ridge. Elytra with striae deeply impressed, each with row of slender, suberect scales; intervals carinate, almost nude, microreticulate; sutural interval basally swollen; interval 7 swollen subapically, laterally weakly projecting. Femora edentate. Metafemur subapically with stridulatory patch and transverse ridge. Abdominal ventrite 5 flat, densely punctate, sparsely setose. Penis (Fig. 89b) with body flattened, in profile +markedly +curved; in dorsal aspect sides subparallel; apex with median, triangular extension; transfer apparatus flagelliform, slightly longer than body; apodemes 2.4 +x +as long as body; ductus ejaculatorius without bulbus. Intraspecific variation. Length 2.10-2.58 mm. Color of body with sutural interval ferruginous or completely black. Body shape slightly more elongate or compact. Female rostrum dorsally with pairs of lateral and submedian furrows; epistome simple. + + + +Material examined. + +Holotype (MZB): ARC2652 (EMBL # LM655910), West Java Prov., Bogor, Cidahu, Mt. Salak (near Javana Spa), sample 3, +S06°43.425' +, +E106°43.227' +, 1756 m, 13-IV-2012. Paratypes (ARC, MZB, SMNK, ZSM): W-Java Prov.: 6 exx, ARC0104, ARC0184 (EMBL # LM655409), Mt. Halimun N.P., Pasir Banteng, Mt. Botol, 1550 m, 17-XI-2004; 3 exx, Mt. Halimun N.P., Citalahab, Mt. Kendeng, 1550 m, 19-XI-2004; 3 exx, ARC2648 (EMBL # LM655906), ARC2649 (EMBL # LM655907), Bogor, Cidahu, Mt. Salak (near Javana Spa), sample 1, +S06°43.733' +, +E106°42.711' +, 1429 m, 13-IV-2012; 5 exx, same data as holotype; 1 ex, ARC2653 (EMBL # LM655911), Sukabumi, Mt. Gede, Cisaat, Situ Gunung, sample 1, +S06°49.377' +, +E106°55.729' +, 1281 m, 15-IV-2012; 1 ex, ARC2663 (EMBL # LM655921), Sukabumi, Mt. Gede, Cisaat, Situ Gunung, sample 5, +S06°47.912' +, +E106°56.457' +, 1940 m, 16-IV-2012; 1 ex, Sukabumi, Mt. Gede, Cisaat, Situ Gunung, sample 4, +S06°48.250' +, +E106°56.271' +, 1720 m, 16-IV-2012; 4 exx, ARC2666 (EMBL # LM655924), Sukabumi, Mt. Gede, Cisaat, Situ Gunung, sample 7, +S06°48.377' +, +E106°56.183' +, 1637 m, 16-IV-2012, under +Lithocarpus +sp.; 1 exx, ARC0159, Garut, Kawah Kamojang, sample 2, +S07°09.578' +, +E107°47.802' +, 1400 m, 26-IX-2005; 2 exx, ARC0182 (EMBL # LM655407), Garut, Kawah Kamojang, sample 3, +S07°09.497' +, +E107°47.828' +, 1430 m, 26-IX-2005; 4 exx, ARC0256 (EMBL # LM655448), ARC0257 (EMBL # LM655449), ARC0258 (EMBL # LM655450), Telaga Warna, between Puncak and Cipanas, sample 1, +S06°42.253' +, +E106°59.755' +, 1585 m, 06-VIII-2006; 11 exx Telaga Warna, between Puncak and Cipanas, sample 2, +S06°42.097' +, +E106°59.833' +, 1477 m, 06-VIII-2006. + + + +Distribution. +W-Java Prov., (Mt. Gede, Mt. Halimun N.P., Kawah Kamojang, Mt. Salak). Elevation: 1400-1940 m. + + +Etymology. +This epithet is based on the Latin adjective suturalis and refers to the basally swollen elytral suture. + + +Notes. + +Trigonopterus suturalis +Riedel, sp. n. was coded as " +Trigonopterus +sp. 304". + + + + \ No newline at end of file diff --git a/data/38/20/B4/3820B4A02DBF960622F5A70A97545651.xml b/data/38/20/B4/3820B4A02DBF960622F5A70A97545651.xml new file mode 100644 index 00000000000..357b0108eab --- /dev/null +++ b/data/38/20/B4/3820B4A02DBF960622F5A70A97545651.xml @@ -0,0 +1,85 @@ + + + +Polychaetes of Greece: an updated and annotated checklist + + + +Author + +Faulwetter, Sarah + + + +Author + +Simboura, Nomiki + + + +Author + +Katsiaras, Nikolaos + + + +Author + +Chatzigeorgiou, Giorgos + + + +Author + +Arvanitidis, Christos + +text + + +Biodiversity Data Journal + + +2017 + +5 + + +20997 +20997 + + + + +http://dx.doi.org/10.3897/BDJ.5.e20997 + +journal article +http://dx.doi.org/10.3897/BDJ.5.e20997 +1314-2828-5-20997 + + + + + +Dipolydora flava ( +Claparede +, 1870) + + + + + +Dipolydora flava +( +Claparede +, 1870) | +Polydora flava +Claparede +, 1870 + + + +Notes +Type locality: Mediterranean (Gulf of Naples). + + + \ No newline at end of file diff --git a/data/38/20/E9/3820E97699EE5209FE0AC2FFA3935D2B.xml b/data/38/20/E9/3820E97699EE5209FE0AC2FFA3935D2B.xml new file mode 100644 index 00000000000..d12635ba464 --- /dev/null +++ b/data/38/20/E9/3820E97699EE5209FE0AC2FFA3935D2B.xml @@ -0,0 +1,202 @@ + + + +Commensal Leucothoidae (Crustacea, Amphipoda) of the Ryukyu Archipelago, Japan. Part III: coral rubble-dwellers + + + +Author + +White, Kristine N. + + + +Author + +Reimer, James Davis + +text + + +ZooKeys + + +2012 + +173 + + +11 +50 + + + + +http://dx.doi.org/10.3897/zookeys.173.2498 + +journal article +http://dx.doi.org/10.3897/zookeys.173.2498 +1313-2970-173-11 + + + + +Paranamixis Schellenberg, 1938 +Figures 13, 14 + + + + +Paranamixis misakiensis +Thomas, 1997: 89-91, fig. 26. + + + +Material examined. + +Anamorph male, 3.5 mm RUMF-ZC-1875, Haruta, Yakushima Island, Kagoshima, reef wall ( +30°18'12"N +, +130°39'28"E +), among coral rubble, 10 m, K.N. White and N.S. White, col., 27 May 2011 (KNWYaku4C). + + + + +Diagnosis +(Anamorph male). + + +Head anterior margin oblique, anterodistal margin oblique with notch; ventral cephalic keel anterior margin oblique with projection and excavation. Antenna 2 longer than antenna 1. Maxilliped inner plates fused +with +apical notch. Gnathopod 1 coxa anterodistal margin subtriangular, bi-cuspidate. Gnathopod 2 coxa broader than long, greatly enlarged, distal margin with anterior and posterior cusps; basis anterior margin with distal serrate ridge; carpus distally +tapered +, anterior margin dentate; dactylus proximal margin dentate with 2 plumose setae. Telson apex rounded. + + + +Description (Anamorph male). + +Head. Anterior margin oblique, anterodistal margin oblique with notch, distal margin rounded; ventral cephalic keel anterior margin oblique with projection and excavation, anteroventral margin quadrate, produced, ventral margin oblique; eyes present with more than 10 ommatidia, round. Antenna 1 0.3 +x +body length, flagellum 7-articulate, peduncle article 1 width less than 2 +x +article 2, accessory flagellum 1-articulate. Antenna 2 0.4 +x +body length, longer than antenna 1, flagellum 3-articulate. Mouthparts reduced. Maxilliped inner plates fused with apical notch; outer plate inner margin smooth, reaching 0.1 +x +palp article 1, bare; palp 4-articulate, article 4 elongate, distally acute. + + +Pereon. Coxae 1-4 relative widths 1.0: 2.9: 1.7: 2.0. Gnathopod 1 absent, coxa smooth, with tiny marginal setae, anterodistal margin produced, subtriangular, bi-cuspidate, distal margin oblique, posterior margin straight, facial setae absent. Gnathopod 2 coxa broader than long, greatly enlarged, smooth, bare, anterior margin rounded, anterodistally rounded, distal margin rounded with anterior and posterior cusps, posterior margin rounded, facial setae absent; basis distally expanded, anterior margin with distal serrate ridge and 7 short setae, posterior margin with 1 posterodistal seta; ischium bare; carpus 0.8 +x +propodus length, curved, distally tapered, anterior margin dentate; propodus with 1 mediofacial setal row above midline, reaching 0.5 +x +propodus length, with 1 row of submarginal setae, posterior margin serrate, palm convex with 3 major and many small tubercles; dactylus curved, proximal margin dentate with 2 plumose setae, anterior margin distally obtuse, reaching 0.3 +x +propodus length. Pereopod 3 coxa length 1.4 +x +width, anterodistal corner overriding distal face of coxa 2, not extending below it, smooth, bare, anterior margin straight, distal margin straight with mid-distal cusp, posterior margin straight, facial setae absent. Pereopod 4 coxa smooth, bare, anterior margin straight, distal margin rounded with anterior and mid-distal cusps, posterior margin excavate, facial setae absent. Pereopods 5-7 coxae facial setae absent; bases width length ratios 1: 1.3, 1: 1.3, 1: 1.4, posterior margins smooth, setose. + + +Pleon. Epimera 1-3 bare; epimeron 3 posteroventral corner quadrate. Uropods 1-3 relative lengths 1.0: 0.8: 0.9. Uropod 1 peduncle 0.9 +x +inner ramus length, outer ramus 0.5 +x +inner ramus length; inner ramus with 4 robust setae, outer ramus with 2 robust setae. Uropod 2 peduncle 0.8 +x +inner ramus length, outer ramus 0.6 +x +inner ramus length; inner and outer rami each with 3 robust setae. Uropod 3 peduncle 1.3 +x +inner ramus length, outer ramus 0.7 +x +inner ramus length; inner ramus bare, outer ramus with one robust seta. Telson 1.1 +x +longer than wide, apex rounded. + + + +Figure 13. +Paranamixis misakiensis +Thomas, 1997, male anamorph, 3.5 mm, RUMF-ZC-1875. + + + + +Figure 14. +Paranamixis misakiensis +Thomas, 1997, male anamorph, 3.5 mm, RUMF-ZC-1875. + + + + +Leucomorph (juvenile and sexually dimorphic characters). +Unknown. + + +Ecology. +Host unknown, presumably in sponges in coral rubble. + + +Relationships. + +Paranamixis misakiensis +appears most closely related to +Paranamixis thomasi +in the cuspate, oblique anterodistal head margin, excavate anterior ventral cephalic keel margin, apically cleft maxilliped inner plates, and enlarged gnathopod 2 coxa. +Paranamixis misakiensis +differs from +Paranamixis thomasi +in the following: ventral cephalic keel +anterior +margin with mid-distal projection; gnathopod 2 basis anterior margin with a much larger serrate ridge, propodus with one mediofacial setal row, dactylus proximal margin and dentate. +Paranamixis denticulus +Kim and Kim, 1991 and +Paranamixis aberro +Hirayama 1983 +also share the oblique, cuspate anterior head margin, but differ in many other aspects. + + + +Remarks. + +Anamorph males of +Paranamixis misakiensis +is white in color with pink stripes along pereonite edges (Figure 15G). This species was collected from Yakushima Island, extending its known range approximately 1000 kilometers. The specimen from Yakushima closely agrees with +Thomas' +1997 description, differing slightly in the ventral cephalic keel, which is excavate with a mid-distal projection, versus excavate in +Thomas' +1997 material. + + + +Figure 15. Color plate of new leucothoid amphipod species. A +Anamixis sentan +sp. n. anamorph male B +Anamixis sentan +sp. n. leucomorph female C +Leucothoe enko +sp. n. D +Leucothoe akaisen +sp. n. E +Leucothoe kebukai +sp. n. F +Leucothoe chiisainame +sp. n. G +Paranamixis misakiensis +Thomas, 1997 H +Leucothoe akuma +sp. n. + + + +Figure 16. Sponge-filled coral rubble. + + + +Distribution. +East China Sea: Yakushima Island (Kagoshima), Japan. Pacific Ocean: Misaki, Miura Peninsula (Kanagawa), Japan. + + + \ No newline at end of file diff --git a/data/38/21/6F/38216FCFEFCAEC9C58074AA6E32C779C.xml b/data/38/21/6F/38216FCFEFCAEC9C58074AA6E32C779C.xml new file mode 100644 index 00000000000..f17343a57d3 --- /dev/null +++ b/data/38/21/6F/38216FCFEFCAEC9C58074AA6E32C779C.xml @@ -0,0 +1,114 @@ + + + +Order Primates + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +111 +184 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Prolemur +Gray 1870 + + + + + + + +Prolemur +Gray 1870 + +, +Proc. Zool. Soc. Lond., 1870: 828 + +. + + + + +Type Species: + +Hapalemur (Prolemur) simus +Gray 1871 + + + + + +Synonyms: + +Prohapalemur +Lamberton 1936 + +. + + + + +Species and subspecies: +1 species: + + +Species + +Prolemur simus +Gray 1871 + + + + + +Discussion: +A synonym of + +Hapalemur + +according to +McKenna and Bell (1997) +; regarded as a full genus by + +Groves (2001 +c +) + +. + + + + \ No newline at end of file diff --git a/data/38/21/CE/3821CE13E3BE578637A525D60336339C.xml b/data/38/21/CE/3821CE13E3BE578637A525D60336339C.xml new file mode 100644 index 00000000000..6aed9f1fde6 --- /dev/null +++ b/data/38/21/CE/3821CE13E3BE578637A525D60336339C.xml @@ -0,0 +1,51 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Chrysomela staphylaea +[ +spec. nov. +] + + + + +C. ovata obscure testacea tota. +Fn. svec. +422. + + + + +Habitat in +Europa. + + + + \ No newline at end of file diff --git a/data/38/22/33/3822334F033D0117F1E431E54B4ECB85.xml b/data/38/22/33/3822334F033D0117F1E431E54B4ECB85.xml new file mode 100644 index 00000000000..6cb8b699a9d --- /dev/null +++ b/data/38/22/33/3822334F033D0117F1E431E54B4ECB85.xml @@ -0,0 +1,106 @@ + + + +Order Soricomorpha + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +220 +311 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Sylvisorex konganensis +Ray and Hutterer 1995 + + + + + + + +Sylvisorex konganensis +Ray and Hutterer 1995 + +, +Ecotropica, 1: 93 + +. + + + + +Type Locality: + +SW +Central African Republic +, Dzanga-Sangha Forest Reserve, unlogged mixed species forest near Kongana Camp [ +02°47'N +, +16°25'E +). + + + + + +Vernacular Names: +Kongana Shrew +. + + + + +Distribution: +High forest in +Central African Republic +and +Republic of Congo +(unpubl.). + + + + +Conservation: +A comparison of 16s rRNA sequences showed a closer relationship to + +S. ollula +(Querouil et al., 2001) + +. + + + + \ No newline at end of file diff --git a/data/38/22/87/382287BE1A4A6C0BFF7A5244FC366B8B.xml b/data/38/22/87/382287BE1A4A6C0BFF7A5244FC366B8B.xml new file mode 100644 index 00000000000..b75803263bb --- /dev/null +++ b/data/38/22/87/382287BE1A4A6C0BFF7A5244FC366B8B.xml @@ -0,0 +1,288 @@ + + + +A new subfamily of Dolichopodidae (Diptera) for Tenuopus Curran, 1924 with description of new species from Tropical Africa + + + +Author + +Grichanov, I. Ya. + +text + + +Far Eastern Entomologist + + +2018 + +2018-08-06 + + +365 + + +1 +25 + + + + +http://dx.doi.org/10.25221/fee.365.1 + +journal article +10.25221/fee.365.1 +2713-2196 +7164252 +02387D27-9229-448B-9727-2C240AB4F04E + + + + + + + +Tenuopus unicolor +(Becker, 1914) + + + + + + + +Figs 6 +, +14 +, +22 + + + + + +Psilopus unicolor +Becker, 1914: 126 + +. +Type +locality: +Kenya +. + + + +Sciapus unicolor +: Becker, 1923: 48 + +. + + + +Tenuopus unicolor +: Dyte & Smith, 1980: 449 + +. + + + + + +TYPE MATERIAL +. +Neotype +, here designated: + +, + +Kenya + +: +Kiambu +Co., +0.932°S +, + + + + +36.616°E +, + +2600 m + +, + +18.XII 2013 + +, +N. Vikhrev +[ +ZMUM +] + +. + + + + +DESCRIPTION. Male. +Head +: frons black, densely brownish pollinose; one pair of well developed postvertical setae; upper postocular setae black, increasing in length upward; lateral and lower postoculars white; ventral postcranium covered with irregular white hairs; face silvery-white, 5 times as high as wide in middle, nearly as wide as postpedicel; clypeus slightly bulging; antennae as long as height of head, + +with yellow scape and pedicel and blackish-brown postpedicel; pedicel projected distally on inner side, with a crown of short black setae, one of dorsal setae as long as pedicel; postpedicel rounded-oval, slightly longer than high at base (1.5/1.2); + +arista-like stylus dorsal, with short hairs; length ratio of scape to pedicel to postpedicel to stylus (1 +st +and 2 +nd +segments), 4/5/6/2/30; palpus and proboscis short, + +yellow, covered with white hairs, proboscis also with a pair of black lateral setae. + +Thorax +: pleura yellow; mesonotum orange, dark medially on posterior part; + + +scutellum dorsally mostly metallic blue-green; 6 dorsocentral setae with posterior pair shifted laterally; acrostichals uniseriate, strong, nearly reaching 5 +th +dorsocentrals; + +scutellum with 2 strong bristles and 2 short lateral hairs; proepisternum with 2 +yellow setae. + +Legs +yellow, slightly darkened distally; tarsi brown from tip of basitarsus; fore and mid coxae with black hairs anteriorly and 5-7 black apical bristles of various length; hind coxa with one long black outer bristle above middle; fore femur with numerous dark fine erect ventral hairs, at most half as long as diameter of femur, + +and 3 long black posteroventral cilia; fore tibia simple, with elongate ventral and posterior setulae, 1 anterodorsal and 1 posterodorsal at base, 1-2 dorsals in middle, + +1-2 apical setae; basitarsus with elongate setulae ventrally, slightly thickened at apex; 2 +nd +to 5 +th +segments with full posteroventral row of strong erect setulae; 2 +nd +to + + +4 +th +segments with 1-2 short dorsoapical setae; claws simple; mid femur with strong anterior preapical seta, with erect black ventral hairs, at most half as long as diameter of femur; mid tibia with 3 anterior, 3 posterodorsal, 3-5 ventral, 4-5 apical setae; + +mid basitarsus with several short ventral setae; hind femur without long hairs, with 1 +strong anterior preapical seta; hind tibia with 3-4 anterior, 2 anterodorsal, 2 +posterodorsal, 3-4 apical setae. Femur, tibia and tarsomere (from first to fifth) +length ratio: fore leg: 17/20/13/10/5/8/3, mid leg: 18/24/15/6/5/3/2, hind leg: +16/26/7/8/4/3/2. + +Wing +greyish, veins brown; subcosta very thin; ratio of part of costa between + + +R +2+3 +and R +4+5 +to that between R +4+5 +and M +1 +, 5/1; M +1 +with gentle arc to apex, reaching costa right before wing apex; M +2 +present as fold on membrane; crossvein +dm-m + + +straight; ratio of crossvein +dm-m +to apical part of M +1+2 +(fork-handle) to apical part of M +4 +, 5/15/15; anal vein foldlike, not reaching wing margin; anal angle obtuse; + +lower calypter yellow, with black apex and pale setae; halter yellow with orange knob, halter stem thin and long, with dorsal and ventral groups of short hairs distally. + +Abdomen +mostly yellow-orange, black setose; 1 +st +segment yellow, with small brown posterior spot dorsally; 2 +nd +– 5 +th +yellow, with black edgings anteriorly and posteriorly; the edgings wider dorsally; 6 +th +, 8 +th +segments and epandrium entirely black; epandrial lobes brown; hypandrium small, simple; phallus thin and simple; 1 + +reduced epandrial lobe bearing 2 long apical setae at base of hypandrium; 1 long epandrial lobe distally bearing small ventral subapical spine; 1 longer distoventral lobe bearing 1 long and 1 short subapical setae and small declinate apical lobule with fringe of 8 setulae at apex; 1 very long and broad sword-shaped striated distoventral lobe, as long as epandrium, bearing small apical spine; surstylus black, long and curved, half as long as epandrium, bearing 1 minute seta on angular apex, 3 short setae at middle and trangular dorsal tooth at middle; cercus yellow, twice longer than epandrium, elongate-rectangular, with toothed distal margin, covered with long, mostly black hairs, denser at apex. +MEASUREMENTS (in mm). Body length 6.0; antenna length 1.5; wing length +6.2; wing width 1.9, hypopygium 1.4. + + + + +DISTRIBUTION. +Type +locality: +Kenya + +. + +DR Congo +, +Kenya + +. + + + + +DIAGNOSIS. + +T. unicolor + +belongs to a group of species with uniseriate acrostichals, being the closest to + +T. shcherbakovi + +, differing from the latter in male and female postpedicel oval, longer than high; male cercus band-like, almost evenly wide (see key above). + + +NOTES. The species was described by a single female taken by the expedition of Ch. Alluaud and R. Jeannel from environs of Mt. +Kenya +at +2400 m +a.s.l. as follows from the original paper of Becker (1914) and from the date of collection (22 + + +January 1912). It was later recorded by females only ( +Grichanov, 1996 +, 2000). The +holotype +must be deposited in the collection of Muséum National d’Histoire + + +Naturelle (Paris, +France +), but it was not found there, as well as in other European museums keeping Becker’s types, being most probably lost. Therefore, I designate here the +neotype +of + +Psilopus unicolor + +collected not far from the type locality. The specimen corresponds to the original description by Becker (1914, 1923) and to the diagnosis of + +Tenuopus unicolor + +female provided by +Grichanov (1996) +. + + + + \ No newline at end of file diff --git a/data/38/22/87/382287BE1A4C6C09FF7A543FFBB96CCA.xml b/data/38/22/87/382287BE1A4C6C09FF7A543FFBB96CCA.xml new file mode 100644 index 00000000000..d929264ebca --- /dev/null +++ b/data/38/22/87/382287BE1A4C6C09FF7A543FFBB96CCA.xml @@ -0,0 +1,258 @@ + + + +A new subfamily of Dolichopodidae (Diptera) for Tenuopus Curran, 1924 with description of new species from Tropical Africa + + + +Author + +Grichanov, I. Ya. + +text + + +Far Eastern Entomologist + + +2018 + +2018-08-06 + + +365 + + +1 +25 + + + + +http://dx.doi.org/10.25221/fee.365.1 + +journal article +10.25221/fee.365.1 +2713-2196 +7164252 + + + + + + + +Tenuopus soderlundi +Grichanov + +, +sp. n. + + + + + + +Figs 26–28 + + + + + +TYPE MATERIAL +. +Holotype +– + +, + +South Africa + +: +Cape Province +, +10 km +S of + + + +Citrusdal, Koomlandskloof, +32°40'S +, +19°01'E +, Malaise-trap, at stream in low indigenous forest, +5–8.X 1994 +, M. Söderlund [ +ZMLU +]. +Paratype +: +1♂ +, +Republic of + + + +South Africa +: +Cape Province +, + +10 km +S of Citrusdal + +, +Koomlandskloof +, +32°40'S + +, + + +19°01'E +, Malaise-trap, fynbos on mountain, +5–7.X 1994 +, Michael Söderlund + + +[ +ZMLU +]. + + + + +DESCRIPTION. Male (somewhat discolorated). +Head +: frons black, shining; one pair of short postvertical setae; upper postocular setae black, slightly increasing in length upward; lateral and lower postoculars white; ventral postcranium covered with irregular white hairs; face silvery-white, 6 times as high as wide in middle, + +nearly as wide as postpedicel; clypeus bulging; antennae as long as height of head, + +with yellow scape and pedicel and orange postpedicel; pedicel projected distally on inner side, with a crown of short black setae, 1-2 dorsal setae longer; postpedicel rounded, as long as high (1/1); arista-like stylus dorsal, with short hairs; length ratio of scape to pedicel to postpedicel to stylus (1 +st +and 2 +nd +segments), 5/6/8/6/39; palpus and proboscis short, yellow, covered with white hairs, proboscis also with a pair of black lateral setae. + + +Thorax +: pleura yellow; mesonotum orange, with median black stripe half as wide as surface between dorsocentral bristles, wider posteriorly; scutellum black dorsally; 6 dorsocentral setae with posterior pair shifted laterally; acrostichals absent; scutellum with 2 strong bristles and 2 short lateral hairs; proepisternum with + +2 long yellow setae. + +Legs +including coxae yellow; tarsi brown from tip of basitarsus; fore and mid coxae with black hairs anteriorly and 4-7 black apical bristles of various length; + +hind coxa with one long black outer bristle above middle; fore leg without remarkable + + +Figs 23–28. + +Tenuopus +spp. + +23–25 – + +T. cognatus +Parent + +; 26–28 – + +T. soderlundi + +sp. n. +; 23, + + +26 – head; 27 – wing; 24, 28 – hypopygium after maceration, right lateral view; 25 – epandrial lobes and surstylus, right lateral view. +hairs and setae; fore tibia simple, with 1 short anterodorsal at base, 1-2 short apical setae; claws simple; mid femur with strong anterior preapical seta; mid tibia with 2- +3 anterior, 3 posterodorsal, 3-5 ventral, 4-5 apical setae; mid basitarsus with several short ventral setae; hind femur without long hairs, with 1 strong anterior preapical seta; hind tibia with 4-5 anterior, 2 anterodorsal, 2 posterodorsal, 3-4 apical setae. +Femur, tibia and tarsomere (from first to fifth) length ratio: fore leg: 13/13/11/5/ +3/2/2, mid leg: 16/21/14/6/4/2/2, hind leg: 19/27/8/9/5/3/2. + +Wing +hyaline, veins yellow; subcosta very thin; ratio of part of costa between + + +R +2+3 +and R +4+5 +to that between R +4+5 +and M +1 +, 4/1; M +1 +with gentle arc to apex, reaching costa far before wing apex; M +2 +present as fold on membrane; crossvein +dm-m + + +straight; ratio of crossvein +dm-m +to apical part of M +1+2 +(fork-handle) to apical part of M +4 +, 2.5/6/11; anal vein foldlike, not reaching wing margin; anal angle obtuse; + +lower calypter yellow, with brown apex and pale setae; halter yellow, halter stem thin and long, with dorsal and ventral groups of short hairs distally. + +Abdomen mostly yellow, black setose; 1 +st +segment yellow, with white hairs ventrally; 5 +th +segment mostly brown, 6 +th +segment black; epandrium yellow-brown; + +surstylus and epandrial lobes brown; hypandrium relatively long, simple; phallus thin and simple; basoventral epandrial lobe reduced to 3 long apical setae at base of hypandrium; 1 long epandrial lobe distally with short setae at apex; 2-3 short setae between basoventral and distoventral lobes; surstylus short, about 1/3 as long as epandrium, strongly sclerotised, paw-shaped, with 4 apical processes; cercus yellow, half as long as epandrium, rounded, with short apical projection, covered with short hairs and several setae. +MEASUREMENTS (in mm). Body length 5-5.2; antenna length 1.1; wing length 4.2; wing width 1.4. +Female. Unknown. + + +ETYMOLOGY. The species is named after the Swedish entomologist, Dr. M. + + +Söderlund ( +ZMLU +), the collector of the +type +specimens + +. + + + + +DISTRIBUTION. +South Africa +. + + + + +DIAGNOSIS. + +T. soderlundi + +sp. n. +is the smallest fly in the genus and belongs to a group of species with uniseriate acrostichals or without acrostichals, being the closest to + +T. cognatus + +, differing from the latter in wing vein M +4 +more than 4 times longer than +dm-m +; abdomen with 2 +nd +–4 +th +segments entirely yellow (see key above). + + + + \ No newline at end of file diff --git a/data/38/22/87/382287BE1A4E6C0DFF7A56FDFEC36A6C.xml b/data/38/22/87/382287BE1A4E6C0DFF7A56FDFEC36A6C.xml new file mode 100644 index 00000000000..8d80e2bfb9e --- /dev/null +++ b/data/38/22/87/382287BE1A4E6C0DFF7A56FDFEC36A6C.xml @@ -0,0 +1,110 @@ + + + +A new subfamily of Dolichopodidae (Diptera) for Tenuopus Curran, 1924 with description of new species from Tropical Africa + + + +Author + +Grichanov, I. Ya. + +text + + +Far Eastern Entomologist + + +2018 + +2018-08-06 + + +365 + + +1 +25 + + + + +http://dx.doi.org/10.25221/fee.365.1 + +journal article +10.25221/fee.365.1 +2713-2196 +7164252 +02387D27-9229-448B-9727-2C240AB4F04E + + + + + + + +Tenuopus maculatus +Parent, 1931 + + + + + + + + +MATERIAL +EXAMINED. +1♀ +, + +Tanzania + +Morogoro +env., +Uluguru Mts + +., + + + +6.84593°S +, +37.692°E +, + +853 m + +, + +17.IX 2012 + +, +D. Gavryushin +[ +ZMUM +] + +. + + + + + +DISTRIBUTION. +Type +locality: +Malawi + +: + +Mt. Mlange. +Kenya, Malawi +, +Tanzania + +. + + + + \ No newline at end of file diff --git a/data/38/22/87/382287BE1A4E6C0FFF7A5526FD2B6B03.xml b/data/38/22/87/382287BE1A4E6C0FFF7A5526FD2B6B03.xml new file mode 100644 index 00000000000..6c6b564cdce --- /dev/null +++ b/data/38/22/87/382287BE1A4E6C0FFF7A5526FD2B6B03.xml @@ -0,0 +1,293 @@ + + + +A new subfamily of Dolichopodidae (Diptera) for Tenuopus Curran, 1924 with description of new species from Tropical Africa + + + +Author + +Grichanov, I. Ya. + +text + + +Far Eastern Entomologist + + +2018 + +2018-08-06 + + +365 + + +1 +25 + + + + +http://dx.doi.org/10.25221/fee.365.1 + +journal article +10.25221/fee.365.1 +2713-2196 +7164252 +02387D27-9229-448B-9727-2C240AB4F04E + + + + + + + +Tenuopus shcherbakovi +Grichanov, 1996 + + + + + + + +Figs 7, 13 +, +21 + + + + + +MATERIAL +EXAMINED. +1♂ +(dried from ethanol and mounted on pin), + +Kenya + + +: + + + +Kakamega +Forest +, +0°22'S +, +34°50'E +, + +1500 m + +, + +3.VI 2000 + +, white pantrap, +M. Kraemer + + + +& G. Velten [ +NMSA +]; + +1♀ +, + +Tanzania + +: +East Uzambara +, +Amani +, + +1000 m + +, + +1.II 1977 + + +, + + +H. Enghoff, O. Lomholdt, O. Martin [ +ZMUC +]. + + + + +DESCRIPTION. Male (somewhat discolorated). +Head +: frons black, pollinose; + +one pair of well developed postvertical setae; upper postocular setae black, slightly increasing in length upward; lateral and lower postoculars white; ventral postcranium covered with irregular white hairs; face silvery-white, 7 times as high as wide in middle, nearly as wide as postpedicel; clypeus bulging; antennae as long as height of head, with yellow scape and pedicel and orange postpedicel; pedicel projected distally on inner side, with a crown of short black setae, one of dorsal setae as long as pedicel; postpedicel subtriangular, as long as high (1/1); arista-like stylus dorsal, + +with short hairs; length ratio of scape to pedicel to postpedicel to stylus (1 +st +and 2 +nd + +segments), 4/5/5/2/34; palpus and proboscis short, yellow, covered with white hairs, +proboscis also with a pair of black lateral setae. + +Thorax +: pleura yellow; mesonotum orange, dark medially on posterior part; + + +scutellum dorsally mostly metallic blue-green; 6 dorsocentral setae with posterior pair shifted laterally; acrostichals uniseriate, strong, nearly reaching 5 +th +dorsocentrals; + +scutellum with 2 strong bristles and 2 short lateral hairs; proepisternum with 1 long and 1 short brown setae. + +Legs +yellow, slightly darkened distally; tarsi brown from tip of basitarsus; fore and mid coxae with black hairs anteriorly and 5-7 black apical bristles of various length; hind coxa with one long black outer bristle above middle; fore femur with numerous dark fine erect ventral hairs, at most half as long as diameter of femur, + +and 3 long black posteroventral cilia; fore tibia simple, with elongate ventral and posterior setulae, 1 anterodorsal and 1 posterodorsal at base, 1-2 dorsals in middle, +1-2 apical setae; basitarsus with elongate setulae ventrally, slightly thickened at apex; + +apical half of 2 +nd +, 3 +rd +to 5 +th +segments with posteroventral row of strong erect setulae; + + +2 +nd +to 4 +th +segments with 1-2 short dorsoapical setae; claws simple; mid femur with strong anterior preapical seta, with semi-erect black ventral hairs in distal half, at most half as long as diameter of femur; mid tibia with 3 anterior, 3 posterodorsal, 3-5 + +ventral, 4-5 apical setae; mid basitarsus with several short ventral setae; hind femur without long hairs, with 1 strong anterior preapical seta; hind tibia with 3-4 anterior, +2 anterodorsal, 2 posterodorsal, 3-4 apical setae. Femur, tibia and tarsomere (from first to fifth) length ratio: fore leg: 11/12/8/6/2/3/3, mid leg: 10/15/9/4/3/2/1, hind leg: 12/20/5/6/3/2/1. + +Wing +greyish, veins brown; subcosta very thin; ratio of part of costa between + + +R +2+3 +and R +4+5 +to that between R +4+5 +and M +1 +, 5/1; M +1 +with gentle arc to apex, reaching costa right before wing apex; M +2 +present as fold on membrane; crossvein +dm-m + + +straight; ratio of crossvein +dm-m +to apical part of M +1+2 +(fork-handle) to apical part of M +4 +, 3/8/8; anal vein foldlike, not reaching wing margin; anal angle obtuse; lower calypter yellow, with brown apex and pale setae; halter yellow with white knob, + +halter stem thin and long, with dorsal and ventral groups of short hairs distally. + + +Figs 19–22. + +Tenuopus +spp. + +, epandrial lobes and surstylus, right lateral view: 19 – +T. kylei + + + +sp. n.; 20 – + +T. lomholdti + +sp. n. +; 21 – + +T. shcherbakovi +Grichanov + +; 22 – + +T. unicolor +(Becker) + +. + + +Abdomen +mostly yellow, black setose; 1 +st +segment yellow; 2 +nd +–5 +th +yellow, with narrow black edgings posteriorly; 6 +th +, 8 +th +segments and epandrium almost entirely black; epandrial lobes brown; hypandrium small, simple; phallus thin and simple; 1 + +short epandrial lobe bearing 2 long apical setae at base of hypandrium; 1 long epandrial lobe distally with 2 arms, with proximal arm bearing minute apical seta and distal arm bearing long apical seta; 1 thin distoventral lobe, as long as bifurcated lobe, bearing 2 short and 1 long setae at apex; 1 very long sword-shaped distoventral lobe, as long as epandrium, bearing 3 short setae, i.e. 1 apical, 1 subapical and 1 +seta at middle of inner side; surstylus black, long and narrow, nearly half as long as epandrium, bearing 3 minute setae in distal half and strong dorsal tooth at middle; +cercus yellow, twice longer than epandrium, elongate-ovate, broadened in basal half, covered with rather short, mostly black hairs, shorter and denser at apex. +MEASUREMENTS (in mm; in ethanol). Body length 7.0; antenna length 1.2; +wing length 5.4; wing width 1.5. + + + + +DISTRIBUTION. +Type +locality: +Uganda +: Namanve. +Kenya +, +Uganda +. +This +species is recorded here from +Tanzania +for the first time + +. + + + + +DIAGNOSIS. The species was originally described by a female ( +Grichanov, + + +1996). Later, its males and females were recorded by +Grichanov +et al. (2011a). One of those males is here described for the first time. + +T. shcherbakovi + +belongs to a group of species with uniseriate acrostichals, being the closest to + +T. unicolor + +, + +differing from the latter in male and female postpedicel subtriangular, as long as high; cercus broadest at base (see key above). + + + \ No newline at end of file diff --git a/data/38/22/87/382287BE1A506C0DFF7A53D4FDD56943.xml b/data/38/22/87/382287BE1A506C0DFF7A53D4FDD56943.xml new file mode 100644 index 00000000000..6b0ad620155 --- /dev/null +++ b/data/38/22/87/382287BE1A506C0DFF7A53D4FDD56943.xml @@ -0,0 +1,251 @@ + + + +A new subfamily of Dolichopodidae (Diptera) for Tenuopus Curran, 1924 with description of new species from Tropical Africa + + + +Author + +Grichanov, I. Ya. + +text + + +Far Eastern Entomologist + + +2018 + +2018-08-06 + + +365 + + +1 +25 + + + + +http://dx.doi.org/10.25221/fee.365.1 + +journal article +10.25221/fee.365.1 +2713-2196 +7164252 + + + + + + + +Tenuopus lomholdti +Grichanov + +, +sp. n. + + + + + + +Figs 5 +, +12 +, +20 + + + + + +TYPE MATERIAL +. +Holotype +– + +, + +Tanzania + +: +East Uzambara +, +Amani +, + +1000 m + +, + + + + + +26.I 1977 + +, +H. Enghoff +, +O. Lomholdt +& +O. Martin +leg. [ +ZMUC +]. +Paratype + +: + +1♂ +(in ethanol), +Tanzania +: +Morogoro +Reg., + +Udzungwa Mt. +N. P. + +, +Mito Mitatu +, +7°50'15.1''S + +, + + + +36°50'49.9''E +, + +1198 m + +, +Malaise trap +, + +17.V 2013 + +, +T +. +Pape +& +N. Scharff +leg. [ +ZMUC +] + +. + + + + +DESCRIPTION. Male. +Head +: frons black, whitish pollinose; one pair of short postvertical setae, as long as uppermost postocular seta; upper postocular setae black, increasing in length upward; lateral and lower postoculars white; ventral postcranium covered with irregular white hairs; face silvery-white, 7 times as high as wide in middle, nearly as wide as postpedicel; clypeus slightly bulging; antennae as long as height of head, with yellow scape and pedicel and yellow-orange postpedicel; pedicel projected distally on inner side, with a crown of short black setae, + + +one of dorsal setae as long as pedicel; postpedicel rounded, slightly longer than high at base (1.5/1.3); arista-like stylus dorsal, with short hairs; length ratio of scape to pedicel to postpedicel to stylus (1 +st +and 2 +nd +segments), 15/17/20/12/92; palpus and proboscis short, yellow, covered with white hairs, proboscis also with a pair of black lateral setae. + + +Thorax +: pleura dirty yellow; mesonotum brownish orange, with narrow black stripe along acrostichals, wider posteriorly and black on scutellum dorsally; 6 + + +dorsocentral setae with posterior pair shifted laterally; acrostichals irregularly biseriate, short, nearly reaching 5 +th +dorsocentrals; scutellum with 2 strong bristles and + +2 short lateral hairs; proepisternum with 2 yellow setae. + +Legs +yellow; last segments of tarsi brown; fore and mid coxae with black hairs anteriorly and 5-7 black apical bristles of various length; hind coxa with one long black outer bristle above middle; fore femur with dark fine erect ventral hairs, at most half as long as diameter of femur, and 1-2 black posteroventral cilia; fore tibia simple, with 1 anterodorsal and 1 posterodorsal at base, 1-2 dorsals in middle, 1-2 + +apical setae; tarsomeres simple, with rather short ventral semi-erect setulae on all segments, with 1-2 elongate dorsal setae on distal apex of segments 1-4; claws simple; mid femur with very small anterior preapical seta, glabrous ventrally; mid tibia with 3 anterior, 3 posterodorsal, 3 ventral, 3-4 apical seta; basitarsus with few short ventral setae; hind femur without long hairs, with 1 strong anterior preapical seta; hind tibia with 3 anterior, 2 dorsal, 3 posterodorsal, 2-3 apical setae; basitarsus with few short posterior setae. Femur, tibia and tarsomere (from first to fifth) length ratio: fore leg: 44/45/35/19/19/21/12, mid leg: 31/50/35/15/11/6/4, hind leg: +28/51/17/15/10/6/3. + +Wing +greyish, veins brown; subcosta very thin; ratio of part of costa between + + +R +2+3 +and R +4+5 +to that between R +4+5 +and M +1 +, 16/2; M +1 +with gentle arc to apex, + + +reaching costa right before wing apex; M +2 +present as fold on membrane; crossvein + + +dm-m +straight; ratio of crossvein +dm-m +to apical part of M +1+2 +(fork-handle) to apical part of M +4 +, 9/31/23; anal vein foldlike, not reaching wing margin; anal angle obtuse; + +lower calypter yellow, with black apex and pale setae; halter yellow with orange knob, halter stem thin and long, with dorsal and ventral groups of short hairs distally. + +Abdomen +mostly yellow-orange, black setose; 2 +nd +–6 +th +yellow, with narrow brown or black posterior edging; 8 +th +segment and epandrium entirely yellow; 8 +th +segment with dark hairs; cerci and surstyli yellow; cercus covered with dark-yellow hairs and setae; surstylus dark at apex; hypandrium small, simple; phallus thin and simple; epandrial lobe prominent, finger-like, pointed at apex, with 4 ventral setae; + +5 epandrial setae of different length between hypandrium and base of epandrial lobe, including 1 thick pedunculate seta; surstylus about as large as cercus, +irregularly leaf-like, with small dorsal process at apex, with 2 inner setae at middle; +cercus about half as long as epandrium, subtriangular, pointed at apex, covered with short hairs dorsally, double row of long setae distally. +MEASUREMENTS (in mm). Body length 5.8; antenna length 1.3; wing length +4.9; wing width 1.4. +Female. Unknown. + + +ETYMOLOGY. The species is named after the Danish entomologist, Dr. O. + +Lomholdt (ZMUC), one of the collectors of the +type +specimens. + + + + +DIAGNOSIS. + +T. lomholdti + +sp. n. +belongs to a group of species with biseriate acrostichals, being the closest to + +T. taitensis + +due to enlarged surstylus, differing from the latter in male cercus subtriangular, without process, surstylus about as large as cercus (see key above). + + + + \ No newline at end of file diff --git a/data/38/22/87/382287BE1A526C13FF7A534AFCAD6C57.xml b/data/38/22/87/382287BE1A526C13FF7A534AFCAD6C57.xml new file mode 100644 index 00000000000..73943272be9 --- /dev/null +++ b/data/38/22/87/382287BE1A526C13FF7A534AFCAD6C57.xml @@ -0,0 +1,238 @@ + + + +A new subfamily of Dolichopodidae (Diptera) for Tenuopus Curran, 1924 with description of new species from Tropical Africa + + + +Author + +Grichanov, I. Ya. + +text + + +Far Eastern Entomologist + + +2018 + +2018-08-06 + + +365 + + +1 +25 + + + + +http://dx.doi.org/10.25221/fee.365.1 + +journal article +10.25221/fee.365.1 +2713-2196 +7164252 + + + + + + + +Tenuopus kylei +Grichanov + +, +sp. n. + + + + + + +Figs 4 +, +11 +, +19 + + + + + +TYPE MATERIAL +. +Holotype +– + +, + +South Africa + +: +Kwazulu +, +Madlangula +, +Kosi + + + + +Bay, + +21.I – 6.II 1985 + +, +R + +. + +Kyle [ +NMSA +]. +Paratype +: +1♂ + +, same label [ +NMSA +]. + + + + +DESCRIPTION. Male. +Head +: frons black, whitish pollinose; one pair of short postvertical setae, as long as uppermost postocular seta; upper postocular setae black, increasing in length upward; lateral and lower postoculars white; ventral postcranium covered with irregular white hairs; face silvery-white, 7 times as high as wide in middle, nearly as wide as postpedicel; clypeus slightly bulging; antennae as long as height of head, with yellow scape and pedicel and yellow-orange postpedicel; pedicel projected distally on inner side, with a crown of short black setae, + +one of dorsal setae as long as pedicel; postpedicel rounded, as long as high at base + +(1/1); arista-like stylus dorsal, with short hairs; length ratio of scape to pedicel to postpedicel to stylus (1 +st +and 2 +nd +segments), 5/7/9/3/40; palpus and proboscis short, + +yellow, covered with white hairs, proboscis also with a pair of black lateral setae. + +Thorax +: pleura yellow; mesonotum mostly orange-yellow, with median greenish blue stripe half as wide as surface between dorsocentral bristles, wider posteriorly and black on scutellum dorsally; 6 dorsocentral setae with posterior pair shifted laterally; acrostichals biseriate, strong, nearly reaching 5 +th +dorsocentrals; scutellum with 2 strong bristles and 2 short lateral hairs; proepisternum with 2 yellow setae. + + +Legs +yellow; last segments of hind tarsus brown; fore and mid coxae with black hairs anteriorly and 5-7 black apical bristles of various length; hind coxa with one long black outer bristle above middle; fore femur with light and dark fine erect ventral hairs, at most half as long as diameter of femur, and 1-2 black posteroventral cilia; fore tibia simple, with 1 anterodorsal and 1 posterodorsal at base, 1 dorsal in middle, 1-2 apical setae; basitarsus with 1 dorsal; other tarsomeres simple; claws simple; mid femur with very small anterior preapical seta, practically glabrous ventrally, with few dark ventral hairs; mid tibia with 3 anterior, 3 posterodorsal, 3 + +ventral, 3-4 apical seta; hind femur without long hairs, with 1 strong anterior preapical seta; hind tibia with 3 anterior, 2 dorsal, 3 posterodorsal, 2-3 apical setae. Femur, +tibia and tarsomere (from first to fifth) length ratio: fore leg: 9/12/15/8/4/2/1, mid leg: 10/15/12/5/4/2/1, hind leg: 12/20/6/6/4/2/1. + + +Figs 15–18. + +Tenuopus +spp. + +, epandrial lobes and surstylus, right (15, 18) and left (16) lateral + + + +view, and cercus, dorsal view (17): 15 – + +T. bururiensis + +sp. n. +; 16–17 – + +T. gorongosaensis + +sp. + + +n.; 18 – + +T. kirkspriggsi + +sp. n. + + +Wing +greyish, almost hyaline, veins brown; subcosta very thin; ratio of part of costa between R +2+3 +and R +4+5 +to that between R +4+5 +and M +1 +, 7/1; M +1 +with gentle arc to apex, reaching costa right before wing apex; M +2 +present as fold on membrane; crossvein +dm-m +straight; ratio of crossvein +dm-m +to apical part of M +1+2 +(fork-handle) to apical part of M +4 +, 5/16/13; anal vein foldlike, not reaching wing margin; anal angle obtuse; lower calypter yellow, with black apex and pale setae; halter yellow with orange knob, halter stem thin and long, with dorsal and ventral groups of short hairs distally. + + +Abdomen +mostly yellow-orange, black setose; 2 +nd +–6 +th +yellow, with narrow brown or black anterior and posterior edging; 8 +th +segment and epandrium entirely yellow; + + +8 +th +segment with yellow hairs; cerci and surstyli yellow; surstylus and epandrial lobe black at apex; cercus covered with dark-yellow hairs and setae; hypandrium small, simple; phallus thin and simple; epandrial lobe prominent, finger-like, + +narrow at apex, with 2 ventral setae; 3 pedunculate epandrial setae of different length and 2 epandrial processes between hypandrium and base of epandrial lobe, +including 1 process with rather long apical seta and 1 slightly longer process with microscopic apical seta; surstylus about as long as cercus, with apical incision, with thin dorsal and thick ventral lobes; dorsal lobe of surstylus with 1 small apical seta; +ventral lobe of surstylus with 2 small apical setae; cercus nearly as long as epandrium, subtriangular, covered with hairs dorsally and setae distally. +MEASUREMENTS (in mm). Body length 6.0; antenna length 1.4; wing length +5.1; wing width 1.6. +Female. Unknown. + + +ETYMOLOGY. The species is named after the South African zoologist, Dr. R. + +Kyle (Ezemvelo KwaZulu Natal Wildlife), the collector of the +type +specimens. + + + + +DISTRIBUTION. +South Africa +. + + + + +DIAGNOSIS. + +T. kylei + +sp. n. +belongs to a group of species with biseriate acrostichals, being the closest to + +T. kononenkoi + +, differing from the latter in male fore basitarsus longer, about 1.3 times as long as fore tibia; and male surstylus bifurcated only at apex, with broad lobes (see key above). + + + + \ No newline at end of file diff --git a/data/38/22/87/382287BE1A556C11FF7A56A7FBBB6BCF.xml b/data/38/22/87/382287BE1A556C11FF7A56A7FBBB6BCF.xml new file mode 100644 index 00000000000..70f888728cb --- /dev/null +++ b/data/38/22/87/382287BE1A556C11FF7A56A7FBBB6BCF.xml @@ -0,0 +1,211 @@ + + + +A new subfamily of Dolichopodidae (Diptera) for Tenuopus Curran, 1924 with description of new species from Tropical Africa + + + +Author + +Grichanov, I. Ya. + +text + + +Far Eastern Entomologist + + +2018 + +2018-08-06 + + +365 + + +1 +25 + + + + +http://dx.doi.org/10.25221/fee.365.1 + +journal article +10.25221/fee.365.1 +2713-2196 +7164252 + + + + + + + +Tenuopus kirkspriggsi +Grichanov + +, +sp. n. + + + + + + +Figs 3 +, +10 +, +18 + + + + + +TYPE MATERIAL +. +Holotype +– + +, + +Burundi + +: +Kayanza Prov. +, +Parc National de la Kibira +, Rwegura Sector, +2°55.320'S +, +29°30.067'E +, + +2237 m + +, + +21–26.XI 2010 + +, A.H. + + + +Kirk-Spriggs / malaise trap, indigenous Afromontane forest [ +BMSA +]. + + + + +DESCRIPTION. Male. +Head +: frons metallic blue-black, weakly pollinose; one pair of short postvertical setae, as long as uppermost postocular seta; upper postocular setae black, increasing in length upward; lateral and lower postoculars white; ventral postcranium covered with irregular white hairs; face silvery-white, 6 times as high as wide in middle, nearly as wide as postpedicel; clypeus slightly bulging; antennae as long as height of head, with yellow scape and pedicel and yellow-brown postpedicel; pedicel projected distally on inner side, with a crown of short black setae, + + +one of dorsal setae as long as pedicel; postpedicel rounded-oval, slightly longer than high at base (1.6/1.3); arista-like stylus dorsal, with short hairs; length ratio of scape to pedicel to postpedicel to stylus (1 +st +and 2 +nd +segments), 4/5/8/3/34; palpus and proboscis short, yellow, covered with white hairs, proboscis also with a pair of black lateral setae. + + +Thorax +: pleura yellow; mesonotum orange, with almost all the surface between dorsocentrals blue-green; scutellum dorsally mostly metallic blue-green; 6 dorsocentral setae with posterior pair shifted laterally; acrostichals biseriate, strong, nearly reaching 5 +th +dorsocentrals; scutellum with 2 strong bristles and 2 short lateral hairs; + +proepisternum with 2 yellow setae. + +Legs +yellow, slightly darkened distally; tarsi brown from tip of basitarsus; fore and mid coxae with black hairs anteriorly and 5-7 black apical bristles of various length; hind coxa with one long black outer bristle above middle; fore femur with numerous dark and light fine erect ventral hairs, at most half as long as diameter of femur, and 3 long black posteroventral cilia; fore tibia simple, with elongate ventral hairs and posterior setulae, 1 anterodorsal and 1 posterodorsal at base, 1-2 apical setae; tarsomeres covered with dense hairs ventrally, elongate setulae dorsally; claws simple; mid femur with strong anterior preapical seta, with erect black ventral hairs, + +at most half as long as diameter of femur; mid tibia with 3 anterior, 3 posterodorsal, +3-5 ventral, 4-5 apical setae; mid basitarsus with several short ventral setae; hind femur without long hairs, with 1 strong anterior preapical seta; hind tibia with 3-4 +anterior, 2 anterodorsal, 2 posterodorsal, 3-4 apical setae. Femur, tibia and tarsomere +(from first to fifth) length ratio: fore leg: 38/46/38/25/19/11/5, mid leg: 43/72/36/ +16/14/7/4, hind leg: 46/71/18/21/11/7/4. + +Wing +greyish, almost hyaline, veins brown; subcosta very thin; ratio of part of costa between R +2+3 +and R +4+5 +to that between R +4+5 +and M +1 +, 14/3; M +1 +with gentle arc to apex, reaching costa right before wing apex; M +2 +present as fold on membrane; + + +crossvein +dm-m +straight; ratio of crossvein +dm-m +to apical part of M +1+2 +(fork-handle) to apical part of M +4 +, 7/23/19; anal vein foldlike, not reaching wing margin; anal angle obtuse; lower calypter yellow, with black apex and pale setae; halter yellow, + +halter stem thin and long, with dorsal and ventral groups of short hairs distally. + +Abdomen +mostly yellow-orange, black setose; 1 +st +segment yellow, with triangular black posterior spot dorsally; 2 +nd +–6 +th +yellow, with broad black edging posteriorly and with small brown dorsal spot anteriorly; 8 +th +segment and epandrium entirely black; cercus and epandrial lobes orange-brown; surstylus black; cercus covered with dark-yellow hairs and setae; hypandrium small, simple; phallus thin and simple; + +ventral epandrial lobes reduced to short lobules or pedunculate setae; distoventral epandrial lobe prominent, narrow, with 3 minute setae in distal half; surstylus about half as long as cercus, simple, strongly sclerotised, curved; cercus about half as long as epandrium, subtriangular, covered with yellow-brown hairs and setae. +MEASUREMENTS (in mm). Body length 6.3; antenna length 1.3; wing length +6.3; wing width 1.9. +Female. Unknown. + + +ETYMOLOGY. The species is named after the South African entomologist, Dr. + + +A.H. Kirk-Spriggs +( +BMSA +), the collector of the +type +specimen + +. + + + + +DISTRIBUTION. +Burundi +. + + + + +DIAGNOSIS. + +T. kirkspriggsi + +sp. n. +belongs to a group of species with biseriate acrostichals, being the closest to + +T. gorongosaensis + +sp. n. +, differing from the latter in male cercus as long as epandrium, swollen at base, narrow at apex (see key above). + + + + \ No newline at end of file diff --git a/data/38/22/87/382287BE1A556C16FF7A5657FE8869EB.xml b/data/38/22/87/382287BE1A556C16FF7A5657FE8869EB.xml new file mode 100644 index 00000000000..5135960535c --- /dev/null +++ b/data/38/22/87/382287BE1A556C16FF7A5657FE8869EB.xml @@ -0,0 +1,123 @@ + + + +A new subfamily of Dolichopodidae (Diptera) for Tenuopus Curran, 1924 with description of new species from Tropical Africa + + + +Author + +Grichanov, I. Ya. + +text + + +Far Eastern Entomologist + + +2018 + +2018-08-06 + + +365 + + +1 +25 + + + + +http://dx.doi.org/10.25221/fee.365.1 + +journal article +10.25221/fee.365.1 +2713-2196 +7164252 +02387D27-9229-448B-9727-2C240AB4F04E + + + + + + + +Tenuopus guttatus +Parent, 1939 + + + + + + + + +MATERIAL +EXAMINED. +1♂ +(in ethanol), [ + +DR Congo + +:] +Zaire +, +Mt. Ilimu + +, + + + +Kivu Prov. +, +1°50’S +, +28°25’E +, + +900–1000 m + +, [ + +X 1993 + +], fogging + +Carapa grandiflora + + +, + + +Th. Wagner [ +NMSA +]. + + + + + +DISTRIBUTION. +Type +locality: +Ghana + +: + +“Obuasi +Ashanti +”. +DR Congo +, +Ghana + +, + + +Ivory Coast +. + + + + \ No newline at end of file diff --git a/data/38/22/87/382287BE1A566C15FF7A55C2FE946BA9.xml b/data/38/22/87/382287BE1A566C15FF7A55C2FE946BA9.xml new file mode 100644 index 00000000000..5b4f8adce97 --- /dev/null +++ b/data/38/22/87/382287BE1A566C15FF7A55C2FE946BA9.xml @@ -0,0 +1,145 @@ + + + +A new subfamily of Dolichopodidae (Diptera) for Tenuopus Curran, 1924 with description of new species from Tropical Africa + + + +Author + +Grichanov, I. Ya. + +text + + +Far Eastern Entomologist + + +2018 + +2018-08-06 + + +365 + + +1 +25 + + + + +http://dx.doi.org/10.25221/fee.365.1 + +journal article +10.25221/fee.365.1 +2713-2196 +7164252 +02387D27-9229-448B-9727-2C240AB4F04E + + + + + + + +Tenuopus erroneus +Parent, 1934 + + + + + + + + +MATERIAL +EXAMINED. +1♀ +(in ethanol), + +South Africa + +: KZN, +Ramsgate + +, + + + +Butterfly sanctuary, +30°53.3'S +/ +30°20.4'E +, + +27.IV–27.VII 2005 + +, +MT +nr. stream, M + +. + + +Mostovski [ +NMSA +]; + +1♀ +(in ethanol), +South Africa +: KZN, Cathedral Peak Nat. Res + +., + + + +Rainbow Gorge, + +1480 m + +, +28°57.60'S +, +29°13.61'E +, + +14.XII 2005 + +– + +29.I 2006 + +, +MT + +, M. + + +Mostovski [ +NMSA +]. + + + + + +DISTRIBUTION. +Type +locality: +South Africa +: +Cape Province +, +Mossel Bay + +. + + +South Africa +. + + + + \ No newline at end of file diff --git a/data/38/22/87/382287BE1A566C15FF7A5658FD2B6A47.xml b/data/38/22/87/382287BE1A566C15FF7A5658FD2B6A47.xml new file mode 100644 index 00000000000..467b162a89b --- /dev/null +++ b/data/38/22/87/382287BE1A566C15FF7A5658FD2B6A47.xml @@ -0,0 +1,134 @@ + + + +A new subfamily of Dolichopodidae (Diptera) for Tenuopus Curran, 1924 with description of new species from Tropical Africa + + + +Author + +Grichanov, I. Ya. + +text + + +Far Eastern Entomologist + + +2018 + +2018-08-06 + + +365 + + +1 +25 + + + + +http://dx.doi.org/10.25221/fee.365.1 + +journal article +10.25221/fee.365.1 +2713-2196 +7164252 +02387D27-9229-448B-9727-2C240AB4F04E + + + + + + + +Tenuopus cognatus +Parent, 1934 + + + + + + + +Figs 23–25 + + + + + +MATERIAL +EXAMINED. +1♂ +, + +RSA + +: KZN, +Royal Natal Nature Park +, +Mahai + + + +Campsite are at: +28°41.386'S +, +28°56.288'E +, +17–18.II 2010 +, A.H. Kirk-Spriggs / + + +Malaise trap (1), straddling Mahai River [ +BMSA +]; + +1♀ +, + +RSA +, + +[ +Eastern Cape +,] + + + +Tsitsikamma N.P., Plaatbos Nat. reserve at: +39°56.137'S +, +23°54.895'E +, 20–22.I + + +2009, A.H. Kirk-Spriggs & S. Otto / malaise trap, indigenous forest [ +BMSA +]. + + + + + +DISTRIBUTION. +Type +locality: +South Africa + +: Natal, Kloof. +South Africa +. + +NOTES. The species was originally illustrated with a line drawing of wing only. +I publish here pictures of the male head and hypopygium for the first time. + + +Tenuopus cognatus + +is remarkable in having long male cerci clinging close to each other and forming a flat tongue (dorsal view). + + + + \ No newline at end of file diff --git a/data/38/22/87/382287BE1A566C17FF7A54E4FC806E5B.xml b/data/38/22/87/382287BE1A566C17FF7A54E4FC806E5B.xml new file mode 100644 index 00000000000..704d909884c --- /dev/null +++ b/data/38/22/87/382287BE1A566C17FF7A54E4FC806E5B.xml @@ -0,0 +1,286 @@ + + + +A new subfamily of Dolichopodidae (Diptera) for Tenuopus Curran, 1924 with description of new species from Tropical Africa + + + +Author + +Grichanov, I. Ya. + +text + + +Far Eastern Entomologist + + +2018 + +2018-08-06 + + +365 + + +1 +25 + + + + +http://dx.doi.org/10.25221/fee.365.1 + +journal article +10.25221/fee.365.1 +2713-2196 +7164252 + + + + + + + +Tenuopus gorongosaensis +Grichanov + +, +sp. n. + + + + + + +Figs 2 +, +9 +, +16, 17 + + + + + +TYPE MATERIAL +. +Holotype +– + +, [ + +Mozambique + +:] +Gorongosa mountain +, + + + +Manica-Sofala Dist., Port. East Africa, +840 m +, gallery forest, +IX 1957 +, Stuckenberg + + +[ + +NMSA +]. +Paratypes + +: + +1♂ +, +1♀ +, same label [ +NMSA +] + +. + + + + +DESCRIPTION. Male. +Head +: frons black, grey pollinose; one pair of short postvertical setae, as long as uppermost postocular seta; upper postocular setae black, + +increasing in length upward; lateral and lower postoculars white; ventral postcranium covered with irregular white hairs; face silvery-white, 7 times as high as wide in middle, nearly as wide as postpedicel; clypeus slightly bulging; antennae as long as height of head, with yellow scape and pedicel and yellow-brown postpedicel; +pedicel projected distally on inner side, with a crown of short black setae, one of dorsal setae as long as pedicel; postpedicel rounded, as long as high at base (1/1); + +arista-like stylus dorsal, with short hairs; length ratio of scape to pedicel to postpedicel to stylus (1 +st +and 2 +nd +segments), 5/5/6/2/32; palpus and proboscis short, yellow, + +covered with white hairs, proboscis also with a pair of black lateral setae. + +Thorax +: pleura dirty yellow; mesonotum brownish orange, with narrow black stripe along acrostichals, wider posteriorly and black on scutellum dorsally; 6 + + +dorsocentral setae with posterior pair shifted laterally; acrostichals irregularly biseriate, short, nearly reaching 5 +th +dorsocentrals; scutellum with 2 strong bristles and 2 short lateral hairs; proepisternum with 2 yellow setae. + + +Legs +yellow; last segments of tarsi brown; fore and mid coxae with black hairs anteriorly and 5-7 black apical bristles of various length; hind coxa with one long black outer bristle above middle; fore femur with only few light fine erect ventral hairs on basal half, and 3 short black posteroventral cilia; fore tibia simple, with 1 + + +anterodorsal and 1 posterodorsal at base, 1-2 apical setae; 3 +rd +to 5 +th +segments with posteroventral row of short semi-erect setulae; claws simple; mid femur with strong anterior preapical seta, practically glabrous ventrally, with microscopic white ventral hairs; mid tibia with 4 anterior, 4 posterodorsal, 3-5 ventral, 4-5 apical setae; + +mid basitarsus with several short ventral setae; hind femur without long hairs, with 1 +strong anterior preapical seta; hind tibia with 5 anterior, 5 posterodorsal, 3-4 apical setae. Femur, tibia and tarsomere (from first to fifth) length ratio: fore leg: +10/11/9/4/3/2/1, mid leg: 13/18/13/5/4/2/1, hind leg: 14/23/9/6/4/2/1. + +Wing +greyish, almost hyaline, veins brown; subcosta very thin; ratio of part of costa between R +2+3 +and R +4+5 +to that between R +4+5 +and M +1 +, 6/1; M +1 +with gentle arc to apex, reaching costa right before wing apex; M +2 +present as fold on membrane; crossvein +dm-m +straight; ratio of crossvein +dm-m +to apical part of M +1+2 +(fork-handle) to apical part of M +4 +, 4/11/13; anal vein foldlike, not reaching wing margin; anal angle obtuse; lower calypter yellow, with black apex and pale setae; halter yellow with orange knob, halter stem thin and long, with dorsal and ventral groups of short hairs distally. + + +Abdomen +mostly yellow-orange, black setose; 1 +st +segment yellow, with narrow black posterior edging; 2 +nd +–5 +th +yellow, with narrow black posterior edging and broad black triangular spot anteriorly; 6 +th +mostly black, yellow distally; 8 +th +segment and epandrium entirely yellow; 8 +th +segment with yellow hairs; cercus and dorsal surstylus yellow, ventral surstylus brown; cercus covered with dark-yellow hairs and setae; hypandrium small, simple; phallus thin and simple; 2 epandrial lobes distally on each side; thick epandrial lobe with 3 apical setae; thin epandrial lobe with 2 apical setae; short epandrial seta close to epandrial lobes; 1 short and 1 long epandrial setae at base of hypandrium; surstylus about as long as cercus, divided in + +2 lobes from base, with both lobes curved towards longitudinal axis of hypopygium; ventral lobe of surstylus with 1 short apical spine; cercus half as long as epandrium, spatulate, slightly expanded distally, covered with long hairs dorsally and distally. +MEASUREMENTS (in mm). Body length 6.3; antenna length 1.3; wing length +5; wing width 1.5. +Female. Similar to male except lacking male secondary sexual characters. Face wider; legs simple; femur, tibia and tarsomere (from first to fifth) length ratio: fore leg: 9/10/9/5/3/2/1, mid leg: 10/16/11/5/3/1.5/1, hind leg: 13/22/8/6/4/2/1. +MEASUREMENTS (in mm). Body length 6.9; wing length 6.1; wing width 2. + + + +ETYMOLOGY. The species is named after the +type +locality. + + + + +DISTRIBUTION. +Mozambique +. + + + + +DIAGNOSIS. + +T. gorongosaensis + +sp. n. +belongs to a group of species with biseriate acrostichals, being the closest to + +T. kirkspriggsi + +sp. n. +, differing from the latter in male cercus half as long as epandrium, subtriangular (see key above). + + +Female is close to + +T. taitensis + +, differing from the latter in hind tibia and basal half of hind basitarsus yellow (see key above). + + + +Figs 7–14. + +Tenuopus +spp. 7 + +– + +T. shcherbakovi +Grichanov + +, head in ethanol with everted + + +mouthparts (abbreviations: clyp – clypeus; lbl – labellum; lbr – labrum; plp – palpus; premnt – + +prementum); 8–14 – hypopygium after maceration, right lateral view: 8 – + +T. bururiensis + +sp. n. +; + + +9 – + +T. gorongosaensis + +sp. n. +; 10 – + +T. kirkspriggsi + +sp. n. +; 11 – + +T. kylei + +sp. n. +; 12 – + +T. lomholdti + + + +sp. n.; 13 – + +T. shcherbakovi +Grichanov + +; 14 – + +T. unicolor +(Becker) + +. + + + + \ No newline at end of file diff --git a/data/38/22/87/382287BE1A5B6C1AFF7A536DFCEE6E76.xml b/data/38/22/87/382287BE1A5B6C1AFF7A536DFCEE6E76.xml new file mode 100644 index 00000000000..e8697ee1bea --- /dev/null +++ b/data/38/22/87/382287BE1A5B6C1AFF7A536DFCEE6E76.xml @@ -0,0 +1,252 @@ + + + +A new subfamily of Dolichopodidae (Diptera) for Tenuopus Curran, 1924 with description of new species from Tropical Africa + + + +Author + +Grichanov, I. Ya. + +text + + +Far Eastern Entomologist + + +2018 + +2018-08-06 + + +365 + + +1 +25 + + + + +http://dx.doi.org/10.25221/fee.365.1 + +journal article +10.25221/fee.365.1 +2713-2196 +7164252 + + + + + + + +Tenuopus bururiensis +Grichanov + +, +sp. n. + + + + + + +Figs 1 +, +8 +, +15 + + + + + +TYPE MATERIAL +. +Holotype +– + +, + +Burundi + +: +Bururi Prov. +, +Res. Nat. Forestière de Kigwena +, +4°05.949'S +, +29°30.455'E +, + +810 m + +, + +17–20.XI 2010 + +, +A.H. Kirk-Spriggs +/ + + + +malaise trap, circumguinean forest [ +BMSA +]. + + + + +DESCRIPTION. Male. +Head +: frons black, whitish pollinose; one pair of short postvertical setae, as long as uppermost postocular seta; upper postocular setae black, increasing in length upward; lateral and lower postoculars white; ventral postcranium covered with irregular white hairs; face silvery-white, 8 times as high as wide in middle, nearly as wide as postpedicel; clypeus slightly bulging; antennae as long as height of head, with yellow scape and pedicel and yellow-orange postpedicel; + + +pedicel projected distally on inner side, with a crown of short black setae, one of dorsal setae as long as pedicel; postpedicel rounded, slightly longer than high at base (2.1/1.7); arista-like stylus dorsal, with short hairs; length ratio of scape to pedicel to postpedicel to stylus (1 +st +and 2 +nd +segments), 5/5/7/2/26; palpus and proboscis short, yellow, covered with white hairs, proboscis also with a pair of black lateral setae. + + + +Figs 1–6. + +Tenuopus +spp. + +, head: 1 – + +T. bururiensis + +sp. n. +; 2 – + +T. gorongosaensis + +sp. n. +; 3 – + + + +T. kirkspriggsi + +sp. n. +; 4 – + +T. kylei + +sp. n. +; 5 – + +T. lomholdti + +sp. n. +; 6 – + +T. unicolor +(Becker) + +. + + + +Thorax +: pleura yellow; mesonotum mostly orange-yellow, with median greenish blue stripe half as wide as surface between dorsocentral bristles, wider posteriorly; + + +scutellum greenish blue dorsally; 6 dorsocentral setae with posterior pair shifted laterally; acrostichals biseriate, strong, nearly reaching 5 +th +dorsocentrals; scutellum with 2 strong bristles and 2 short lateral hairs; proepisternum with 2 yellow setae. + + +Legs +yellow; last segments of hind tarsus brown; fore and mid coxae with black hairs anteriorly and 5-7 black apical bristles of various length; hind coxa with one long black outer bristle above middle; fore femur with light fine erect ventral hairs, + +at most as long as diameter of femur, longer at apex, and 1 long black posteroventral cilia; fore tibia simple, with 1 anterodorsal and 1 posterodorsal at base, 2 dorsals in middle, 1-2 apical setae; basitarsus with 2 dorsals; other tarsomeres simple; claws simple; mid femur with small anterior preapical seta, with white ventral hairs, at most as long as diameter of femur; mid tibia with 3 anterior, 3 posterodorsal, 3 ventral, 3- +4 apical seta; hind femur without long hairs, with 1 strong anterior preapical seta; +hind tibia with 3 anterior, 2 dorsal, 6 posterodorsal, 2-3 apical setae. Femur, tibia and tarsomere (from first to fifth) length ratio: fore leg: 14/16/18/10/7/3/2, mid leg: +17/25/17/8/6/3/1, hind leg: 14/25/9/8/5/2/1. + +Wing +greyish, almost hyaline, veins brown; subcosta very thin; ratio of part of costa between R +2+3 +and R +4+5 +to that between R +4+5 +and M +1 +, 11/1; M +1 +with gentle arc to apex, reaching costa right before wing apex; M +2 +present as fold on membrane; + + +crossvein +dm-m +straight; ratio of crossvein +dm-m +to apical part of M +1+2 +(fork-handle) + + +to apical part of M +4 +, 4/12/10; anal vein foldlike, not reaching wing margin; anal angle obtuse; lower calypter yellow, with black apex and pale setae; halter yellow with orange knob, halter stem thin and long, with dorsal and ventral groups of short hairs distally. + + +Abdomen +mostly yellow-orange, black setose; 2 +nd +–5 +th +yellow, with narrow black posterior edging; 6 +th +, 8 +th +segment and epandrium entirely yellow; 8 +th +segment with yellow hairs; cerci and surstyli yellow; surstylus and epandrial lobe black at apex; + +cercus covered with dark-yellow hairs and setae; hypandrium small, simple; phallus thin and simple; epandrial lobe prominent, somewhat expanded distally, with 3 apical setae; 2 pedunculate epandrial setae of different length and 3 fused epandrial processes between hypandrium and base of epandrial lobe, including 1 process with rather long apical seta, 1 process with microscopic apical seta and 1 shorter process with moserately long seta; surstylus about as long as cercus, with apical incision, with thin pointed dorsal and thick ventral lobes; dorsal lobe of surstylus with 1 microscopic apical seta; ventral lobe of surstylus with 1 small inner seta; cercus as long as epandrium, subtriangular, with pointed apex, covered with hairs dorsally and few setae distally. +MEASUREMENTS (in mm). Body length 7.5; antenna length 1.7; wing length +6.6; wing width 1.9. +Female. Unknown. + + + +ETYMOLOGY. The species is named after the +type +locality. + + + + +DISTRIBUTION. +Burundi +. + + + + +DIAGNOSIS. + +T. bururiensis + +sp. n. +belongs to a group of species with biseriate acrostichals, being the closest to + +T. fursovi + +, differing from the latter in male fore tarsus simple, male surstylus broad (see key above). + + + + \ No newline at end of file diff --git a/data/38/22/87/382287BE1A5D6C1EFE6E5562FC776AE7.xml b/data/38/22/87/382287BE1A5D6C1EFE6E5562FC776AE7.xml new file mode 100644 index 00000000000..d05372aa2db --- /dev/null +++ b/data/38/22/87/382287BE1A5D6C1EFE6E5562FC776AE7.xml @@ -0,0 +1,82 @@ + + + +A new subfamily of Dolichopodidae (Diptera) for Tenuopus Curran, 1924 with description of new species from Tropical Africa + + + +Author + +Grichanov, I. Ya. + +text + + +Far Eastern Entomologist + + +2018 + +2018-08-06 + + +365 + + +1 +25 + + + + +http://dx.doi.org/10.25221/fee.365.1 + +journal article +10.25221/fee.365.1 +2713-2196 +7164252 +02387D27-9229-448B-9727-2C240AB4F04E + + + + + + +Genus + +Tenuopus +Curran, 1924 + + + + + + + + +Tenuopus +Curran, 1924: 228 + +. + + + + +Type +species: + +Saucropus univittatus +Loew, 1858 + +[ +sensu +Curran, misidentification] = + +Tenuopus erroneus +Parent, 1934 + +, by original designation. + + + + \ No newline at end of file diff --git a/data/38/22/91/382291F6D6465530ABF1E56E57BB7036.xml b/data/38/22/91/382291F6D6465530ABF1E56E57BB7036.xml new file mode 100644 index 00000000000..69411f03292 --- /dev/null +++ b/data/38/22/91/382291F6D6465530ABF1E56E57BB7036.xml @@ -0,0 +1,223 @@ + + + +The snakeflies of the Mediterranean islands: review and biogeographical analysis (Neuropterida, Raphidioptera) + + + +Author + +Aspoeck, Horst +https://orcid.org/0000-0001-9407-3566 +Institute of Specific Prophylaxis and Tropical Medicine, Medical Parasitology, Medical University of Vienna, Kinderspitalgasse 15, 1090 Vienna, Austria + + + +Author + +Aspoeck, Ulrike +Natural History Museum Vienna, Department of Entomology, Burgring 7, 1010 Vienna, Austria & Department of Evolutionary Biology, University of Vienna, Djerassiplatz 1, 1030 Vienna, Austria +ulrike.aspoeck@nhm-wien.ac.at + +text + + +Deutsche Entomologische Zeitschrift + + +2023 + +2023-05-03 + + +70 + + +1 + + +175 +218 + + + + +http://dx.doi.org/10.3897/dez.70.101559 + +journal article +http://dx.doi.org/10.3897/dez.70.101559 +1860-1324-1-175 +9E52FBF7700E4FC3A62E0334CE3DE926 +88E9CFE5B5315143B11AAA90BD90ECBF + + + + + +Phaeostigma +Navas +, 1909, s.l. + + + + + +Phaeostigma +Navas +, 1909 (described as a section of +Raphidia +L.) [type species by subsequent designation: +Raphidia notata +Fabricius, 1781]: + +U. +Aspoeck +and H. +Aspoeck +1989 + +(syst); U. +Aspoeck +and H. + +Aspoeck +1990 + +(syst); H. + +Aspoeck +et al. 1991 + +(mon); +Oswald and Penny 1991 +(cat, nom); +Wachmann and Saure 1997 +(charact); H. + +Aspoeck +et al. 2001 + +(anncat); H. + +Aspoeck +2002 + +(biol, paras); U. + +Aspoeck +2002 + +(compmorph); + +H. +Aspoeck +and U. +Aspoeck +2007 + +(ill: map); +Monserrat and Papenberg 2010 +(bibliogr, biogeogr, biol, chorol, descr, distr, synlist, tax); +Haring et al. 2011 +(fig:distrmap; phyl, phyltree); U. + +Aspoeck +et al. 2012 + +(fig: phyltree; list); + +H. +Aspoeck +and U. +Aspoeck +2013 + +(cat, etymol, phyl), +2014 +(cat); +Monserrat and Papenberg 2015 +(mon). + + + +Taxonomy and systematics. + +H. + +Aspoeck +et al. (1991) + +, +Haring et al. (2011) +. With 41 species and +Subilla three +additional subspecies, + +Phaeostigma + +is (after + +Mongoloraphidia + +) the second largest genus of the family (and of the order). It comprises nine subgenera, seven of these with altogether 12 species are also represented on Mediterranean islands. + +Phaeostigma + +is morphologically clearly differentiated. Based on molecular phylogeny it is the sister group of the rest of the + +Phaeostigma + +clade, i.e. ( + +Subilla + ++ + +Ulrike + +) + [( + +Tjederiraphidia + ++ + +Dichostigma + +) + + +Raphidia + +] ( +Haring et al. 2011 +). The phylogeny of the subgenera of + +Phaeostigma + +has not yet been studied; so far only considerations based upon morphological criteria are available (H. + +Aspoeck +et al. 1991 + +). + + + +Biology. + +Larvae of many species corticolous, of many other species soil-dwelling. Development usually two or +Subilla three +years. Last hibernation stage: full-grown larva. Adults: IV-VII(VIII). + + + +Distribution. + +The distribution of + +Phaeostigma + +s.l. comprises Europe (except the northernmost parts of the continent, the largest part of the Iberian Peninsula, Sicily, Sardinia, Corsica and several islands in the Aegean Sea) as far as to the Ural, Anatolia, the Caucasus region, Lebanon, Syria, northern Iraq, northern Iran. Several Mediterranean islands harbor at leastone species: Levkas, Kefalonia, Thasos, Skopelos, Euboea, Crete, Karpathos, Ikaria, Samos, Lesbos, Chios, Rhodes, Cyprus. + + + + \ No newline at end of file diff --git a/data/38/22/9C/38229C463C39BB3EBF1A0E68123D76EE.xml b/data/38/22/9C/38229C463C39BB3EBF1A0E68123D76EE.xml new file mode 100644 index 00000000000..bc70286ba41 --- /dev/null +++ b/data/38/22/9C/38229C463C39BB3EBF1A0E68123D76EE.xml @@ -0,0 +1,131 @@ + + + +Taxonomic comments on the treatment of the Zygaenidae (Lepidoptera) in volume 3 of Moths of Europe, Zygaenids, Pyralids 1 and Brachodids (2012) + + + +Author + +Efetov, Konstantin A. +Crimean State Medical University, Department of Biological Chemistry and Laboratory of Biotechnology, 295006, Simferopol, Crimea; efetov. konst @ gmail. com + + + +Author + +Hofmann, Axel +Am Hochgestade 5, D- 76351 Linkenheim-Hochstetten, Germany; hofmann @ abl-freiburg. de + + + +Author + +Tarmann, Gerhard M. +Crimean State Medical University, Department of Biological Chemistry and Laboratory of Biotechnology, 295006, Simferopol, Crimea; efetov. konst @ gmail. com + + + +Author + +Tremewan, Walter Gerald +Department of Life Sciences, Division of Insects, Natural History Museum, Cromwell Road, London SW 7 5 BD, U. K.; Correspondence address: Pentreath, 6 Carlyon Road, Playing Place, Truro, Cornwall TR 3 6 EU, U. K.; wgt. pentreath @ btinternet. com +wgt.pentreath@btinternet.com + +text + + +Nota Lepidopterologica + + +2014 + +2014-09-08 + + +37 + + +2 + + +123 +133 + + + + +http://dx.doi.org/10.3897/nl.37.7940 + +journal article +http://dx.doi.org/10.3897/nl.37.7940 +2367-5365-2-123 +384F4C620E0E4B66B7203177920ABA23 +36194B53FA0A536EB10436F822658257 +575701 + + + + + +Adscita +(Adscita) geryon geryon ( +Huebner +, [1813]) + + + + + +Sphinx geryon +Huebner +, [1813], Sammlung +europaeischer +Schmetterlinge 2: pl. 28, figs 130, 131. Type-locality. Europe [Germany]. + + +Adscita geryon razza aeris +Verity, 1946, Redia 31: 154. Type-locality. France: [Alpes-Maritimes], +Saint-Barnabe +. +Syn. rev. + + +Adscita geryon parisiensis +Leraut, 2012, Moths of Europe 3: 62, pl. 6, figs 17, 18. Type-locality. France: Paris region. +Syn. n. + + + +Distribution and taxonomic notes. + + +Adscita geryon geryon + +is distributed from the Iberian Peninsula and Britain to European Russia, the Crimea and Turkey. +Leraut (2012 +: 61) reinstated the nominal taxon + +Adscita geryon aeris + +(Verity, 1946) as valid and on the following page newly described a subspecies from the Paris region. It is acknowledged that + +Adscita geryon + +is an extremely variable species, both in phenotype and genitalic morphology, but we see no justification for recalling a subspecies from synonymy, where it was placed by +Efetov and Tarmann (1999 +: 28, +2012 +: 31), or in describing a new subspecies from France. Accordingly, both taxa are here formally placed as synonyms ( +syn. rev. +; +syn. n. +) of the nominotypical subspecies + +Adscita geryon geryon + +. + + + + \ No newline at end of file diff --git a/data/38/22/F4/3822F42927B8608737EA9148419EFB44.xml b/data/38/22/F4/3822F42927B8608737EA9148419EFB44.xml new file mode 100644 index 00000000000..3d7b9f35c63 --- /dev/null +++ b/data/38/22/F4/3822F42927B8608737EA9148419EFB44.xml @@ -0,0 +1,197 @@ + + + +Flora Helvetica - Oleaceae + + + +Author + +Konrad Lauber + + + +Author + +Gerhart Wagner + + + +Author + +Andreas Gygax + +text + + +2018 +Haupt Verlag + +Bern + + + +Flora Helvetica + + + +922 +926 + + + +book chapter +978-3-258-08047-5 + + + + + +Fraxinus ornus +L. + + + + + +Artbeschreibung: Bis +10 m +hoher Baum + +mit grauen Knospen. +Blaetter +gefiedert + +, mit 2-4 Fiederpaaren. +Teilblaetter +eifoermig +bis lanzettlich, fein +gezaehnt +, unterseits auf dem Mittelnerv behaart, alle gestielt, das +endstaendige +am +laengsten +. + +Blueten +in straussartigen Rispen, stark duftend, mit den +Blaettern +erscheinend + +. + +Kronblaetter +2 oder 4, weiss + +, lineal-lanzettlich, +7-15 mm +lang. Kelch 4teilig. +Fruechte +aehnlich +wie bei + +F. excelsior + +, aber kleiner. + + + + +Bluetezeit +: 4-6 + + +Standort und Verbreitung in der Schweiz: +Waelder +, buschige +Haenge +/ kollin(-montan) / TI, sonst angepflanzt und z.T. verwildert + + + + +Verbreitung global: +Suedeuropaeisch-westasiatisch + + + + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +maessig +trocken +Lichtzahl LhalbschattigSalzzeichen--
Reaktionszahl Rneutral bis basisch (pH 5.5-8.5)Temperaturzahl Twarm-kollin
+Naehrstoffzahl +N + +naehrstoffarm + +Kontinentalitaetszahl +K + +subozeanisch bis subkontinental (mittlere Luftfeuchtigkeit, +maessige +Temperaturschwankungen und +maessig +tiefe Wintertemperaturen) +
+
+
+ + +Volksname Deutscher Name: +Manna-Esche +, +Blumen-Esche +Nom +francais +: + +Frene +a +fleurs + +, +Orne +Nome italiano: +Frassino da manna + + +
+
\ No newline at end of file diff --git a/data/38/23/29/3823297E2252FFA47271FB59FC53FD91.xml b/data/38/23/29/3823297E2252FFA47271FB59FC53FD91.xml new file mode 100644 index 00000000000..9e1d42b536b --- /dev/null +++ b/data/38/23/29/3823297E2252FFA47271FB59FC53FD91.xml @@ -0,0 +1,298 @@ + + + +Phylogenetic studies of the subgenus Petrophilus Chaudoir (Coleoptera: Carabidae: Pterostichus), with description of a new species sympatric with P. thunbergi Morawitz + + + +Author + +Sasakawa, Kôji + + + +Author + +Kubota, Kôhei + +text + + +Zootaxa + + +2006 + +1357 + + +31 +43 + + + +journal article +10.5281/zenodo.174608 +d684512b-4567-4ad3-a2fd-bcd23bc6b953 +1175-5326 +174608 + + + + + + +Subgenus + +Petrophilus +Chaudoir, 1838 + + + + + + + + + +Petrophilus + +Chaudoir, 1838 +: 9 + + +, +type +species: + +Feronia findeli +Dejean + +, by original designation. + +Jedliċka 1962 +: 260 + +. + +Hůrka 1996 +: 278 + +. + +Bousquet 2003 +: 505 + +. + + + + + +Euryperis +Motschulsky, 1850 + +: ix, +type +species: + +Euryperis uralensis +Motschulsky + +, by original designation. + +Jedliċka 1962 +: 255 + +. Synonymy established by + +Kryzhanovskij +et al. +(1995) + +. + + + + + +Morphnosoma + +Lutshnik, 1915 +: 424 + + +, +type +species: + +Carabus vulgaris +Linné + +(= + +Carabus melanarius +Illiger + +), by original designation. + + +Kryzhanovskij +et al. +1995 + +: 105 + +. + +Hůrka 1996 +: 276 + +. + +Bousquet 1999 +: 133 + +. + +Arnett & Thomas 2001 +: 88 + +. + +Bousquet 2003 +: 499 + +. + +Sasakawa & Kubota 2005 +: 390 + +. +Syn. nov. + + + + + +Euferonia + +Casey, 1918 +: 365 + + +, +type +species: + +Feronia stygica +Say + +, by original designation. + +Bousquet 1999 +: 135 + +. + +Arnett & Thomas 2001 +: 88 + +. + +Bousquet 2003 +: 494 + +. Synonymy established, under the subgenus + +Morphnosoma + +, by + +Kryzhanovskij +et al. +(1995) + +. + + + + + +Feroperis + +Lafer, 1979 +: 5 + + +, +type +species: + +Feronia jungens +Tschitschérine + +, by original designation. + + +Kryzhanovskij +et al. +1995 + +: 106 + +. + +Bousquet 2003 +: 495 + +. Synonymy established by + +Kryzhanovskij +et al. +(1995) + +. + + + +Moritapterus +Berlov, 2000 +: 4, +type +species: + +Pterostichus thunbergi +Morawitz + +, by original designation. Synonymy established, under the subgenus + +Morphnosoma + +, by +Sasakawa & Kubota (2005) +. + + + + +Description. +Body medium to large (minimum 10.0 mm: + +P. findeli + +[see +Hùrka 1996 +]; maximum 20.0 mm: + +P. melanarius + +[see +Bousquet 1999 +]). Head normal-sized. Pronotum wide and convex; laterobasal impressions single. Elytra oblong and convex; shoulders distinct. Male sternum 7 without sexual characteristics. Aedeagus stout, bent at approximately 90 degrees at the basal third. Endophallus large and strongly bent ventrally; gonopore weakly sclerotized, without a gonoporal piece; 3 lobes present in all species, one on the left ventrolateral surface near the gonopore, one on the left lateral surface near the gonopore, and one on the right ventrolateral surface near the gonopore; the surface of the lobe on the right ventrolateral surface near the gonopore sclerotized; the ventral surface with transverse pigmentation, except for +P. l a c h r y m o s u s +. + + + + \ No newline at end of file diff --git a/data/38/23/29/3823297E2253FFA77271FD54FC86FDA9.xml b/data/38/23/29/3823297E2253FFA77271FD54FC86FDA9.xml new file mode 100644 index 00000000000..c37f316d70a --- /dev/null +++ b/data/38/23/29/3823297E2253FFA77271FD54FC86FDA9.xml @@ -0,0 +1,180 @@ + + + +Phylogenetic studies of the subgenus Petrophilus Chaudoir (Coleoptera: Carabidae: Pterostichus), with description of a new species sympatric with P. thunbergi Morawitz + + + +Author + +Sasakawa, Kôji + + + +Author + +Kubota, Kôhei + +text + + +Zootaxa + + +2006 + +1357 + + +31 +43 + + + +journal article +10.5281/zenodo.174608 +d684512b-4567-4ad3-a2fd-bcd23bc6b953 +1175-5326 +174608 + + + + + + + +Pterostichus +( +Petrophilus +) +tuberifer +Sasakawa + +, +sp. nov. + + + + +Figs 12–13 +, +17–21 + + + + + + +Pterostichus thunbergi + +(part): + +Tanaka, 1985 +: 110 + +. + + + + + +Pterostichus thunbergi + +(part): + +Kimoto & Yasuda, 1995 +: 280 + +. + + + + + +Diagnosis. +Externally similar to small individuals of + +P. thunbergi + +, but easily distinguished from them by less punctate laterobasal impressions of the pronotum and the presence of a lobe on the middle dorsal surface of the endophallus. + + + + +Description. +Length of body: ɗ, +11.4–13.9 mm +(mean ± SD: 12.3 ± +0.51 mm +) n=20; Ψ, +11.9–14.2 mm +(mean ± SD: 12.6 ± +0.79 mm +) n=12. Dorsal surface of the body black and shiny without metallic luster ( +Figs 17–18 +). Legs reddish to dark brown. + +Head of normal size; mandible with surface grooved; submentum with 2 pairs of setae. Pronotum cordate; surface smooth except for laterobasal impressions; laterobasal impressions weakly wrinkled and sometimes slightly punctuate; hind angle obtuse, without a denticulate tooth. Elytra oblong; shoulders distinct but not denticulate; scutellar stria present but not connected to stria 1; 1 dorsal pore at the anterior end of stria 1; 3 dorsal pores on interval 3; apices of elytra simple, not denticulate. Ventral side almost smooth. + +Aedeagus without a conspicuous tubercle, bent at about 90 degrees at the basal third ( +Fig. 19 +); apical part narrowly rounded on dorsal view ( +Fig. 20 +); membranous part near the ostium not lobate, but slightly sclerotized around the left dorsolateral surface near the ostium. Right paramere slender, bent at about 90 degrees at almost the basal half ( +Fig. 21 +); left paramere wide, square. Endophallus ( +Figs 12–13 +) large, strongly bent ventrally, but not in touch with the ventral surface of the aedeagus; middle dorsal surface lobate; 3 lobes on the left side near the gonopore, one on the ventrolateral surface, one on the lateral surface, and one on the dorsolateral surface; right ventrolateral surface near gonopore with a small and weakly sclerotized lobe; transverse pigmentation on the ventral surface; gonopore weakly sclerotized, without a gonoporal piece. + +Vagina without conspicuous pigmentation; spermatheca elongate, with the basal part distinctly pigmented; apical part of the spermatheca strongly bent at the part connected with the spermathecal gland; stylomere long and stout, with 1 seta on the medial side; lateral side of the stylomere with 2 setae; stylomere apex with 2 nematiform setae. + + + + +Holotype +. + +ɗ, Mt. Hirayama, Shirataki-mura, Hokkaido, +Japan +, +6–14. vii. 2003 +, H. Matsumoto leg., ( +FZUT +0013) [ +FZUT +]. + + + +Paratypes +. + +16ɗɗ9ΨΨ, same data as +holotype +; 3ɗɗ3ΨΨ, Akisato-ikku, Okoppe-chô, Hokkaido, +1–2. viii. 2004 +, K. Sasakawa leg. [ +FZUT +and +NHML +]. + + + + +Etymology. +The specific name derives from the Latin noun +tuber +, +-eris +, n (a swelling, protuberance) and the Latin adjectival suffix +-fer +, +-fera +, +-ferum +(bearing). It refers to the lobe on the middle dorsal surface of the endophallus. + + + + \ No newline at end of file diff --git a/data/38/23/3F/38233FDE8A4F08D723D864A553A8E32A.xml b/data/38/23/3F/38233FDE8A4F08D723D864A553A8E32A.xml new file mode 100644 index 00000000000..06bf3d7280c --- /dev/null +++ b/data/38/23/3F/38233FDE8A4F08D723D864A553A8E32A.xml @@ -0,0 +1,111 @@ + + + +Family-group names in Coleoptera (Insecta) + + + +Author + +Bouchard, Patrice + + + +Author + +Bousquet, Yves + + + +Author + +Davies, Anthony E. + + + +Author + +Alonso-Zarazaga, Miguel A. + + + +Author + +Lawrence, John F. + + + +Author + +Lyal, Chris H. C. + + + +Author + +Newton, Alfred F. + + + +Author + +Reid, Chris A. M. + + + +Author + +Schmitt, Michael + + + +Author + +Ślipinski, S. Adam + + + +Author + +Smith, Andrew B. T. + +text + + +ZooKeys + + +2011 + +88 + + +1 +972 + + + + +http://dx.doi.org/10.3897/zookeys.88.807 + +journal article +http://dx.doi.org/10.3897/zookeys.88.807 +1313-2970-88-1 + + + + +Subfamily +Pterotinae LeConte, 1861 + + + + +Pterotini +J. L. LeConte, 1861: 185 [stem: Pterot-]. Type genus: +Pterotus +J. L. LeConte, 1859. + + + + \ No newline at end of file diff --git a/data/38/23/87/382387A63370261CFE0CFEB7BF822975.xml b/data/38/23/87/382387A63370261CFE0CFEB7BF822975.xml new file mode 100644 index 00000000000..505b6e80efb --- /dev/null +++ b/data/38/23/87/382387A63370261CFE0CFEB7BF822975.xml @@ -0,0 +1,134 @@ + + + +New Cenozoic dragonflies from the Most Basin and Středohoří Complex volcanic area (Czech Republic, Germany) + + + +Author + +Prokop, Jakub +Faculty of Science, Department of Zoology, Charles University in Prague, Praha 2, Czech Republic; + + + +Author + +Pecharová, Martina +Faculty of Science, Department of Zoology, Charles University in Prague, Praha 2, Czech Republic; + + + +Author + +Nel, André +Muséum national d’histoire naturelle, Institut de systématique, évolution, biodiversité, ISYEB, UMR 7205 CNRS UPMC EPHE, CP 50, Sorbonne Universités, Paris, France + +text + + +Journal of Natural History + + +2016 + +2016-05-31 + + +50 + + +2311 +2326 + + + + +http://dx.doi.org/10.1080/00222933.2016.1193648 + +journal article +21211 +10.1080/00222933.2016.1193648 +0accf87d-7caf-45ef-9d8f-fa2e868a88a9 +1464-5262 +3993016 +7A3BB1C3-5A70-4058-86A5-731B58C0ADC3 + + + + + + +Aeshnidae + +genus incertae sedis + + + + +Genus and species undetermined + + + + + +( +Figure 4 +(a, b)) + + + + + +Material + + + +Specimen No. ZD 282 (midpart of hind wing preserved in light brown claystone), deposited in the collections of the Bílina Mine Enterprises, Bílina, +Czech Republic +. + + + + + + +Age +and outcrop + + + + +Early Miocene (Burdigalian), Most Basin, Most Formation, Holešice Member, Delta Sandy Horizon, Bílina mine near Bílina ( +Figure 1 +), +Czech Republic +(see +Kvaček et al. 2004 +). + + + + + +Description + + + +Mid part of a hind wing, fragment +c +. +22 mm +long and +13.9 mm +wide; eight preserved postnodal veins, not well aligned with subpostnodal crossveins; four visible antenodal crossveins not aligned with corresponding crossveins between ScP and RA; four preserved crossveins between RA and RP basal of subnodus; well defined and curved Mspl with four rows of cells between it and MA; two rows of cells between MA and RP3/ +4 in +distal part of this area; one visible Bq crossvein; oblique crossvein + +O + +just distal of base of RP2; Rspl well defined and slightly curved; several secondary posterior branches of IR2 between it and Rspl. + + + + \ No newline at end of file diff --git a/data/38/23/87/382387A63372261DFDE3FCFABEEC2832.xml b/data/38/23/87/382387A63372261DFDE3FCFABEEC2832.xml new file mode 100644 index 00000000000..db3d790a4bf --- /dev/null +++ b/data/38/23/87/382387A63372261DFDE3FCFABEEC2832.xml @@ -0,0 +1,183 @@ + + + +New Cenozoic dragonflies from the Most Basin and Středohoří Complex volcanic area (Czech Republic, Germany) + + + +Author + +Prokop, Jakub +Faculty of Science, Department of Zoology, Charles University in Prague, Praha 2, Czech Republic; + + + +Author + +Pecharová, Martina +Faculty of Science, Department of Zoology, Charles University in Prague, Praha 2, Czech Republic; + + + +Author + +Nel, André +Muséum national d’histoire naturelle, Institut de systématique, évolution, biodiversité, ISYEB, UMR 7205 CNRS UPMC EPHE, CP 50, Sorbonne Universités, Paris, France + +text + + +Journal of Natural History + + +2016 + +2016-05-31 + + +50 + + +2311 +2326 + + + + +http://dx.doi.org/10.1080/00222933.2016.1193648 + +journal article +21211 +10.1080/00222933.2016.1193648 +0accf87d-7caf-45ef-9d8f-fa2e868a88a9 +1464-5262 +3993016 +7A3BB1C3-5A70-4058-86A5-731B58C0ADC3 + + + + + +cf. + +Aeshna + +sp. + + + +( +Figure 3 +(a, b)) + + + + + +Material + + + + +SMMG +Ku +398 (a nearly complete fore wing lacking base and parts along posterior margin, preserved in brown diatomite), collection of +Senckenberg Naturhistorische Sammlungen Dresden +, +Saxony +, +Germany + +. + + + + +Figure 3. +cf. + +Aeshna + +sp. ( +Aeshnidae +), (A) photograph of specimen SMMG Ku 398 (Senckenberg Naturhistorische Sammlungen Dresden coll., Germany), imprint only; (B) line drawing of fore wing. Scale bars represent 5 mm. + + + + + + +Age +and outcrop + + + + +Early Oligocene (Rupelian + +Chattian), +Ústí +Formation, Středohoří Complex, Kundratice near Litoměřice ( +Figure 1 +), +Czech Republic +(see +Kvaček and Walther 1998 +). + + + + + +Description + + + +A nearly complete fore wing, with only basal anterior area and parts along posterior wing margin missing; wing surface apparently hyaline; wing +c +. +52 mm +long (assumed from fragment) and +17.5 mm +wide; distance from estimated base to nodus +c +. +25.3 mm +; distance from nodus to wing apex, +c +. +26.6 mm +; nodus nearly midway between base and apex; distance from nodus to pterostigma +17.4 mm +; distance from pterostigma to apex about +5.6 mm +; pterostigma rather long, 4.0 mm long and +0.9 mm +wide, covering approximately five cells; pterostigmal brace obliquely aligned with proximal side of pterostigma; 20 postnodal cross-veins, not well aligned with 16 visible subpostnodal cross-veins; 12 visible antenodal crossveins of first row between C and ScP not aligned with one visible corresponding antenodal cross-veins of second row between ScP and RA; hypertriangle crossed by three or more cross-veins; median space free, partly preserved; submedian space crossed by two cross-veins, subdiscoidal triangle twocelled; discoidal triangle elongate and divided into five small cells, its costal side being +6.6 mm +long, distal side +5.9 mm +long and proximal side +2.8 mm +long; width of postdiscoidal area just behind discoidal triangle +3.4 mm +, width along posterior wing margin +7.2 mm +; three rows of cells in postdiscoidal area just distal of discoidal triangle; convex supplementary sector (trigonal planate) in postdiscoidal area, aligned with concave Mspl; Mspl well defined, undulated; two or three rows of cells between Mspl and MP and also between Mspl and MA; bulge in distal part of MA ( + +aeshnid bulla + +) apparently weaker than in + +Aeshna zlatkokvaceki + +sp. nov. +, but it is too poorly preserved to be accurately described; five preserved Bq cross-veins; oblique vein + +O + +one cell distal of base of RP2; Rspl well defined and nearly straight; area between Rspl and IR2 with three rows of cells in its widest part; IR2 smoothly curved distally and asymmetrically forked 5.0 mm proximad of pterostigma, with three rows of cells between its branches; RP2 strongly curved posteriorly opposite proximal side of pterostigma; one row of cells between RP2 and anterior branch of IR2; IR1 nearly straight beginning just below proximal posterior edge of pterostigma; one row of cells between MP and CuAa in basal parts, but with about five or six along posterior wing margin; CuAa with circa six posterior branches directed towards posterior wing margin, but not preserved; cubitoanal area poorly preserved, but distinctly broad with about seven rows of cells below CuAa. + + + + \ No newline at end of file diff --git a/data/38/23/87/382387A633752619FE03FCD4BA1C2E3D.xml b/data/38/23/87/382387A633752619FE03FCD4BA1C2E3D.xml new file mode 100644 index 00000000000..8a80e77ac44 --- /dev/null +++ b/data/38/23/87/382387A633752619FE03FCD4BA1C2E3D.xml @@ -0,0 +1,82 @@ + + + +New Cenozoic dragonflies from the Most Basin and Středohoří Complex volcanic area (Czech Republic, Germany) + + + +Author + +Prokop, Jakub +Faculty of Science, Department of Zoology, Charles University in Prague, Praha 2, Czech Republic; + + + +Author + +Pecharová, Martina +Faculty of Science, Department of Zoology, Charles University in Prague, Praha 2, Czech Republic; + + + +Author + +Nel, André +Muséum national d’histoire naturelle, Institut de systématique, évolution, biodiversité, ISYEB, UMR 7205 CNRS UPMC EPHE, CP 50, Sorbonne Universités, Paris, France + +text + + +Journal of Natural History + + +2016 + +2016-05-31 + + +50 + + +2311 +2326 + + + + +http://dx.doi.org/10.1080/00222933.2016.1193648 + +journal article +21211 +10.1080/00222933.2016.1193648 +0accf87d-7caf-45ef-9d8f-fa2e868a88a9 +1464-5262 +3993016 +7A3BB1C3-5A70-4058-86A5-731B58C0ADC3 + + + + + +Genus + +Aeshna +Fabricius, 1775 + + + + + + +Type +species: + +Aeshna vulgatissima +(Linnaeus, 1758) + +designated by +Kirby, 1890 + + + + \ No newline at end of file diff --git a/data/38/23/87/382387A63375261FFE04FC65BCEC2D9F.xml b/data/38/23/87/382387A63375261FFE04FC65BCEC2D9F.xml new file mode 100644 index 00000000000..63fa2e5ecff --- /dev/null +++ b/data/38/23/87/382387A63375261FFE04FC65BCEC2D9F.xml @@ -0,0 +1,198 @@ + + + +New Cenozoic dragonflies from the Most Basin and Středohoří Complex volcanic area (Czech Republic, Germany) + + + +Author + +Prokop, Jakub +Faculty of Science, Department of Zoology, Charles University in Prague, Praha 2, Czech Republic; + + + +Author + +Pecharová, Martina +Faculty of Science, Department of Zoology, Charles University in Prague, Praha 2, Czech Republic; + + + +Author + +Nel, André +Muséum national d’histoire naturelle, Institut de systématique, évolution, biodiversité, ISYEB, UMR 7205 CNRS UPMC EPHE, CP 50, Sorbonne Universités, Paris, France + +text + + +Journal of Natural History + + +2016 + +2016-05-31 + + +50 + + +2311 +2326 + + + + +http://dx.doi.org/10.1080/00222933.2016.1193648 + +journal article +21211 +10.1080/00222933.2016.1193648 +0accf87d-7caf-45ef-9d8f-fa2e868a88a9 +1464-5262 +3993016 +7A3BB1C3-5A70-4058-86A5-731B58C0ADC3 + + + + + + +Aeshna zlatkokvaceki + +sp. nov. + + + + + +( +Figure 2 +(a, b)) + + + + +Figure 2. + +Aeshna zlatkokvaceki + +sp. nov. +( +Aeshnidae +) (A) Photograph of holotype specimen SMMG CsT 1091 (Senckenberg Naturhistorische Sammlungen Dresden coll., Germany), imprint only; (B) line drawing of fore wing. Scale bars represent 5 mm. + + + + + +Etymology + + + +The epithet honours Prof. Zlatko Kvaček (Charles University, +Praha +), a world-famous palaeobotanist who systematically evaluated plant macrofossils from this locality. + + + + + + +Holotype + + + + + +SMMG +CsT 1091 (a nearly complete fore wing preserved in salmon-pink baked clay + +porcelanite), collection of +Senckenberg Naturhistorische Sammlungen Dresden +, +Saxony +, +Germany +. + + + + + + + +Age +and outcrop + + + + +Early Miocene (Burdigalian), Most Basin, Most Formation, Libkovice Member, Želénky near Duchcov ( +Figure 1 +), +Czech Republic +(see +Kvaček and Hurník 2000 +). + + + + + +Description + + + +A nearly complete fore wing, with only median area and extreme apex missing; whole wing surface apparently hyaline; wing +c +. +55 mm +long (assumed from fragment) and +11.6 mm +wide; distance from estimate base to nodus +c +. +26.6 mm +; distance from nodus to wing apex, +c +. +28.2 mm +; nodus nearly midway between base and apex; distance from nodus to pterostigma +16.3 mm +; distance from pterostigma to apex about +7.5 mm +; pterostigma rather long, +4.4 mm +long and +0.9 mm +wide, covering approximately three cells and a half; pterostigmal brace slightly obliquely aligned with proximal side of pterostigma; 11 postnodal cross-veins, not well aligned with 13 visible subpostnodal cross-veins; 19 visible antenodal crossveins of first row between C and ScP not aligned with the 17 visible corresponding antenodal cross-veins of second row between ScP and RA; 13 secondary antenodal cross-veins between Ax2 and nodus; four antenodal crossveins between Ax2 and Ax1; Ax1 +4.6 mm +and Ax2 +10.9 mm +from wing base; hypertriangle crossed by four cross-veins; median space not preserved; submedian space crossed by five cross-veins, subdiscoidal triangle three-celled; discoidal triangle elongate and divided into six smaller cells, its costal side being +8.1 mm +long, distal side +6.9 mm +long and proximal side +3.7 mm +long; width of postdiscoidal area just behind discoidal triangle +3.4 mm +, width along posterior wing margin +7.2 mm +; three rows of cells in postdiscoidal area just distal of discoidal triangle; a short convex supplementary sector (trigonal planate) in postdiscoidal area, aligned with concave Mspl; Mspl well defined, nearly straight in its basal half but slightly curved in distal part; three rows of cells between Mspl and MP and three rows between Mspl and MA; two rows of cells and a short zigzagged supplementary vein in distal part of area between MA and RP3/4; bulge in distal part of MA ( + +aeshnid bulla + +) weak but present; four preserved Bq cross-veins; oblique vein + +O + +one cell distal of base of RP2; Rspl well defined and nearly straight; area between Rspl and IR2 wide, with four rows of cells in its widest part; space between IR2 and Rspl basally divided by oblique intercalary veinlets; IR2 smoothly curved distally and asymmetrically forked just basal of pterostigma, with three rows of cells between its branches; RP2 strongly curved posteriorly opposite proximal side of pterostigma; one row of cells between RP2 and anterior branch of IR2; IR1 present but zigzagged and short, about +8.7 mm +long, beginning just below distal side of pterostigma; one row of cells between MP and CuAa in basal parts but five rows along posterior wing margin; CuAa with circa five posterior branches directed towards posterior wing margin; cubitoanal area broad with six rows of cells below CuAa. + + + + \ No newline at end of file diff --git a/data/38/23/87/382387A6337D2610FE43FE48BFBC2918.xml b/data/38/23/87/382387A6337D2610FE43FE48BFBC2918.xml new file mode 100644 index 00000000000..0bb3892ec2f --- /dev/null +++ b/data/38/23/87/382387A6337D2610FE43FE48BFBC2918.xml @@ -0,0 +1,177 @@ + + + +New Cenozoic dragonflies from the Most Basin and Středohoří Complex volcanic area (Czech Republic, Germany) + + + +Author + +Prokop, Jakub +Faculty of Science, Department of Zoology, Charles University in Prague, Praha 2, Czech Republic; + + + +Author + +Pecharová, Martina +Faculty of Science, Department of Zoology, Charles University in Prague, Praha 2, Czech Republic; + + + +Author + +Nel, André +Muséum national d’histoire naturelle, Institut de systématique, évolution, biodiversité, ISYEB, UMR 7205 CNRS UPMC EPHE, CP 50, Sorbonne Universités, Paris, France + +text + + +Journal of Natural History + + +2016 + +2016-05-31 + + +50 + + +2311 +2326 + + + + +http://dx.doi.org/10.1080/00222933.2016.1193648 + +journal article +21211 +10.1080/00222933.2016.1193648 +0accf87d-7caf-45ef-9d8f-fa2e868a88a9 +1464-5262 +3993016 +7A3BB1C3-5A70-4058-86A5-731B58C0ADC3 + + + + + +? + +Onychothemis rihai +Prokop et al., 2003 + + + + + + +( +Figure 6 +(a, b)) + + + + + +Material + + + +Specimen no. TN1 stored in private collection of Mgr. Tomáš Novotný, Nástup Tušimice quarry, +Czech Republic +. + + + + + + +Age +and outcrop + + + + +Early Miocene (Burdigalian), Libouš mine ( +Figure 1 +), Spořice district, Most Basin, Most Formation, Libkovice Member, about + +15 + +20 m + +above the Crandallite Horizon C1 +sensu +Matys-Grygar & Mach (2013). + + + + + +Description + + + +Fore wing. Wing hyaline, +51.6 mm +long; distance between base and nodus +26.6 mm +; between nodus and apex +25.3 mm +, nodus nearly midway between base and apex; distance between nodus and pterostigma +16.3 mm +, between pterostigma and apex +4.3 mm +; pterostigma +5.9 mm +long, +0.9 mm +wide, with costal and posterior sides maximally widened in middle; no oblique pterostigmal brace; pterostigma covering three and a half cells; 11 postnodal cross-veins, not well aligned with eight corresponding postsubnodal cross-veins; + +libellulid gap + +long; second oblique cross-vein between RP1 and RP2 only weakly oblique; 15 preserved antenodal cross-veins of first row, apparently all well aligned with those of second row, last antenodal cross-vein incomplete; distance between first antenodal crossvein and wing base +6.9 mm +; distance between arculus and wing base +5.6 mm +; arculus opposite an antenodal cross-vein (probably second one, but incompletely preserved); number of cross-veins between RA and RP, between arculus and nodus, unknown; one preserved Bq cross-vein between IR2 and RP2; distance between arculus and nodus +20.6 mm +; base of RP 3/4 and that of IR2 +16.9 mm +distal of arculus; sectors of arculus (bases of RP and MA) clearly fused basally; median and submedian spaces free of crossveins, subdiscoidal cell +3.6 mm +long, +2.2 mm +wide and divided into five cells; discoidal triangle narrow transverse, divided into two cells, length of its costal side +1.3 mm +; proximal side +4.3 mm +long, distal side 5.0 mm long; 2 + +3 rows of cells in anal area; 3 + +5 rows of cells in cubito-anal area, width of cubito-anal area +2.5 mm +; CuA not well defined and reaching posterior wing margin about 3.0 mm basal of nodus; MP nearly straight and reaching posterior wing margin +3.2 mm +distal of nodus; four rows of cells in postdiscoidal area just distal of discoidal triangle; postdiscoidal area narrower ( +2.8 mm +wide) in its middle part than near discoidal triangle ( +3.9 mm +wide); Mspl straight, with one row of cells between it and MA; RP 3/4 and MA basally nearly straight but distally curved and nearly perpendicular to posterior wing margin; RP2 aligned with subnodus; oblique cross-vein + +O + +1.1 mm +distal of subnodus; IR2 and RP2 with two strong undulations; IR2 and RP2 distally curved and nearly perpendicular to wing margin; area between IR2 and RP3/4 rather wide, with a nearly straight vein Rspl; two rows of cells between Rspl and IR2; area between RP1 and RP2 rather wide, but incompletely preserved, no visible + +reversed libellulid oblique vein + +between RP2 and RP3/4. + + + + \ No newline at end of file diff --git a/data/38/23/87/382387A6337D2611FE1CFED2BCEE2C23.xml b/data/38/23/87/382387A6337D2611FE1CFED2BCEE2C23.xml new file mode 100644 index 00000000000..658c6e4aeda --- /dev/null +++ b/data/38/23/87/382387A6337D2611FE1CFED2BCEE2C23.xml @@ -0,0 +1,80 @@ + + + +New Cenozoic dragonflies from the Most Basin and Středohoří Complex volcanic area (Czech Republic, Germany) + + + +Author + +Prokop, Jakub +Faculty of Science, Department of Zoology, Charles University in Prague, Praha 2, Czech Republic; + + + +Author + +Pecharová, Martina +Faculty of Science, Department of Zoology, Charles University in Prague, Praha 2, Czech Republic; + + + +Author + +Nel, André +Muséum national d’histoire naturelle, Institut de systématique, évolution, biodiversité, ISYEB, UMR 7205 CNRS UPMC EPHE, CP 50, Sorbonne Universités, Paris, France + +text + + +Journal of Natural History + + +2016 + +2016-05-31 + + +50 + + +2311 +2326 + + + + +http://dx.doi.org/10.1080/00222933.2016.1193648 + +journal article +21211 +10.1080/00222933.2016.1193648 +0accf87d-7caf-45ef-9d8f-fa2e868a88a9 +1464-5262 +3993016 +7A3BB1C3-5A70-4058-86A5-731B58C0ADC3 + + + + + +Genus + +Onychothemis +Brauer, 1868 + + + + + + +Type +species: + +Onychothemis abnormis +Brauer, 1868 + + + + + \ No newline at end of file diff --git a/data/38/23/87/382387A6337F2612FE75FE2CBF342FDA.xml b/data/38/23/87/382387A6337F2612FE75FE2CBF342FDA.xml new file mode 100644 index 00000000000..7e74e69bd2d --- /dev/null +++ b/data/38/23/87/382387A6337F2612FE75FE2CBF342FDA.xml @@ -0,0 +1,165 @@ + + + +New Cenozoic dragonflies from the Most Basin and Středohoří Complex volcanic area (Czech Republic, Germany) + + + +Author + +Prokop, Jakub +Faculty of Science, Department of Zoology, Charles University in Prague, Praha 2, Czech Republic; + + + +Author + +Pecharová, Martina +Faculty of Science, Department of Zoology, Charles University in Prague, Praha 2, Czech Republic; + + + +Author + +Nel, André +Muséum national d’histoire naturelle, Institut de systématique, évolution, biodiversité, ISYEB, UMR 7205 CNRS UPMC EPHE, CP 50, Sorbonne Universités, Paris, France + +text + + +Journal of Natural History + + +2016 + +2016-05-31 + + +50 + + +2311 +2326 + + + + +http://dx.doi.org/10.1080/00222933.2016.1193648 + +journal article +21211 +10.1080/00222933.2016.1193648 +0accf87d-7caf-45ef-9d8f-fa2e868a88a9 +1464-5262 +3993016 +7A3BB1C3-5A70-4058-86A5-731B58C0ADC3 + + + + + + +? + +Ictinogomphus + + +species undetermined + + + + + +( +Figure 5 +(a, b)) + + + + +? + +Ictinogomphus +Cowley, 1934 + +: +Prokop and Fikáček 2007 +, p. 210, fig. 1 + + + + + +Material + + + + +SMMG +SaT 532, collection of +Senckenberg Naturhistorische Sammlungen Dresden +, +Saxony +, +Germany + +. + + + + +Figure 5. +? + +Ictinogomphus + +species indet. ( +Lindeniidae +), (A) Photograph of specimen under film layer of ethyl alcohol SMMG SaT 532 (Senckenberg Naturhistorische Sammlungen Dresden coll., Germany); (B) line drawing of fore wing. Scale bar represent 5 mm. + + + + + + +Age +and outcrop + + + + +Early Oligocene (Rupelian), Seifhennersdorf ( +Saxony +, +Germany +) ( +Figure 1 +), inter-bedded brownish diatomite within the magmatic complex, equivalent of the Loučeň Formation (see +Walther and Kvaček 2007 +). + + + + + +Description + + + +Distal two-third of a hyaline fore wing, about +29.2 mm +long, +9.4 mm +wide; distance between nodus and pterostigma +11.5 mm +, between pterostigma and wing apex +3.2 mm +; pterostigma +5.7 mm +long, +1.14 mm +wide, covering six cells; pterostigmal brace oblique; three rows of cells in postdiscoidal area between triangle and posterior branch of MA; MA and IR2 both with a very distinct diverging posterior branch; 12 postnodal cross-veins, not aligned with postsubnodal cross-veins; two rows of cells between MA and RP3/4 near posterior wing margin; four rows of cells between MP and CuA along posterior wing margin; five rows of cells between CuA and posterior wing margin. + + + + \ No newline at end of file diff --git a/data/38/23/88/3823883CFF90FFB3FF293BAD24E8FD43.xml b/data/38/23/88/3823883CFF90FFB3FF293BAD24E8FD43.xml new file mode 100644 index 00000000000..2d22e2d54cb --- /dev/null +++ b/data/38/23/88/3823883CFF90FFB3FF293BAD24E8FD43.xml @@ -0,0 +1,1243 @@ + + + +A new species of Ergasilus von Nordmann, 1832 (Copepoda: Cyclopoida) from the gills of a dasyatid ray, Himantura oxyrhyncha (Sauvage, 1878) from West Kalimantan, Indonesia + + + +Author + +Boxshall, Geoffrey A. + +text + + +Zootaxa + + +2016 + +4174 + + +1 + + +93 +103 + + + +journal article +38059 +10.11646/zootaxa.4174.1.6 +6acdd2a8-d032-4fbd-9c90-aabbbbad9048 +1175-5326 +160023 +1F0F6D0F-9D03-43D3-A0E9-7054A6F1001D + + + + + + + +Ergasilus kimi + +sp. nov. + + + + +( +Figs. 1–3 +) + + + + + + +Type +material. + +Holotype +ovigerous + +from gills of + +Himantura oxyrhyncha + +(KA 229) caught in the +Java +Sea off the coast of +West Kalimantan +, +Indonesia +, near +Sungai Kakap +( +00°03’42.38”S +, +109°10’37.68”E +) on + +18 July 2007 + +; registration number +MZB +Cru Cop 113 + +. + +Paratype + +from gills of + +H. oxyrhyncha + +(KA 186) caught in the +Java +Sea off the coast of +West Kalimantan +, +Indonesia +, near +Jungkat +( +00°03’46.00”N +, +109°12’10.40”E +) on + +13 July 2007 + +; registration number +MZB +Cru Cop 114 + +. + +Paratype + +from gills of + +H. oxyrhyncha + +(KA 236) caught in the +Java +Sea off the coast of +West Kalimantan +, +Indonesia +, near +Sungai Kakap +( +00°03’42.38”S +, +109°10’37.68”E +) on + +18 July 2007 + +; registration number + +USNM +1266274 + + +. + +Paratype + +from gills of + +H. oxyrhyncha + +(KA 186) caught in the +Java +Sea off the coast of +West Kalimantan +, +Indonesia +, near +Jungkat +( +00°03’46.00”N +, +109°12’10.40”E +) on + +13 July 2007 + +, partly dissected; registration number + +NHMUK +2014.661 + +. + + + + + +Etymology. +The species is named in honour of Professor Il-Hoi Kim in recognition of his contributions to our knowledge of the +Ergasilidae +of the +Northern +Indo-Pacific. + + + + +Description of adult female. +Body cyclopiform ( +Fig. 1 +A), comprising prosome consisting of cephalosome and first pedigerous somite, separated dorsally by functional articulation but fused ventrally, and three free pedigerous somites (bearing legs 2 to 4), and urosome consisting of fifth pedigerous somite, genital double-somite and three free abdominal somites. Cephalosome elongate, covered by dorsal shield; with oral region located ventrally near posterior border and separated from antennary bases by distinct gap. Rostrum ( +Fig. 1 +C) weakly developed, ornamented with median pore and two pairs of sensillae. First pedigerous somite elongate, narrower than cephalosome. Second pedigerous somite narrower than first, bearing paired, weakly defined integumental windows laterally on tergite (arrowed in +Fig. 1 +A). Third pedigerous somite narrower than second, and fourth narrower than third; tergite of fourth pedigerous somite completely concealing fifth pedigerous somite in dorsal view ( +Fig. 1 +A). Fifth pedigerous somite very small, concealed in both dorsal and ventral views. Genital double somite, 1.2 times wider than long, with rounded lateral margins, bearing paired, slit-like genital apertures dorsally, ornamented with transverse rows of spinules on ventral surface ( +Fig. 1 +B). First and second free abdominal somites broad and short, both ornamented with posterior spinule row along ventral margin. Anal somite deeply incised in midline; about 2.5 times broader than long: ornamented with paired spinule rows on ventral surface ( +Fig. 1 +B). Caudal rami about 1.4 times longer than wide: armed with four setae, all naked ( +Fig. 1 +B). Mean body length from anterior margin of cephalothorax to posterior margin of caudal rami 619 µm (range 614–625 µm, based on three specimens). Egg sacs multiseriate, length 575 and 606 µm in +holotype +. + + +Antennule 6-segmented ( +Fig. 2 +A), setal formula: 3, 12, 5, 4 + ae, 2 + ae, 7 + ae. Antenna 4-segmented ( +Fig. 2 +B) comprising robust coxobasis armed with short naked seta distally, 3-segmented endopod and curved terminal claw. Second segment (first endopodal segment) unarmed but with small swelling near middle of medial margin carrying tiny sensilla. Third segment (second endopodal segment) shorter and narrower than preceding segment, curved distally and bearing small tooth-like process on medial margin about one third of length from base. Fourth segment (third endopodal segment) reduced, bearing minute seta externally. Claw curved, without fossa on concave margin; length of claw about equal to length of second endopodal segment. + + +Labrum weakly defined, with slightly concave posterior margin ( +Fig. 2 +C). Mandible ( +Fig. 2 +D) with three blades; proximal blade carried on posterior margin, ornamented with 12 blunt teeth increasing in size distally; subapical blade ornamented with row of about 12 large pointed spinules on posterior margin and isolated spinules on anterior margin; apical blade slender, tapering, with fine spinules. Maxillule ( +Fig. 2 +E) lobate, armed with two unequal distal setae and produced into small process medially. Maxilla ( +Fig. 2 +F) comprising large tapering syncoxa and basis; syncoxa ornamented with patch of spinules and single pore; basis spatulate and ornamented with dense array of acute spinules. Maxilliped absent, as in all female ergasilids. + + +Legs 1–4 ( +Figs. 3 +A–D) biramous, each with 3-segmented endopod and 3-segmented exopod, except for 2- segmented exopod of leg 4. Intercoxal sclerites slender, interpodal plates well developed between legs 1 and 2, legs 2 and 3 and legs 3 and 4; each ornamented with row of large spinules posteriorly ( +Fig. 1 +D). Spine and seta formula as follows: + + +Coxa Basis Exopod Endopod Legs 1–4 with outer margins of all endopodal and exopodal segments ornamented with row of spinules; inner margin of first exopodal segment with row of long spinules. Legs 1 to 4 each with row of spinules on basis, near inner posterior margin ( +Figs. 3 +A–D); leg 1 with additional row of minute spinules adjacent to origin of endopod ( +Fig. 3 +A). + + + + + + + + + + + + + + + + + + + + + + + +
Leg 1 0-01-0I-0; 0-1; II,5 0-1; 0-1; II,4
Leg 2 0-01-0I-0; 0-1; 6 0-1; 0-2; I,4
Leg 3 0-01-0I-0; 0-1; 6 0-1; 0-2; I,4
Leg 4 0-01-0I-0; 5 0-1; 0-2; I,3
+
+ +Fifth leg ( +Fig. 1 +E) located dorso-laterally and visible in dorsal view; indistinctly 2-segmented; first segment with single (protopodal) seta located and directed dorsally, second (exopodal) segment about 1.4 times longer than wide, ornamented with minute spinules distally, and armed with two long setae; apical seta reaching beyond posterior margin of caudal ramus. + + +Taxonomic remarks. +The new species has 153 congeners and recent studies have shown the genus + +Ergasilus + +to be very heterogeneous and in need of revision ( +El-Rashidy 1996 +; + +Song +et al. +2008 + +). The current classification is based almost entirely on characteristics of the adult females, so species such as + +E. divergens +( +Kokubo, 1914 +) + +, which is known only from the male ( + +Ohtsuka +et al. +2004 + +), cannot be compared with the new species. The combination of a 3-segmented endopod for leg 1 and the presence of two setae on the free exopodal segment of leg 5, is relatively unusual within the genus, and the new species thus belongs in an assemblage of 28 nominal species of + +Ergasilus + +which share these two character states: + +E. batai +Karamchandani, 1952 + +; + +E. borneoensis +Yamaguti, 1954 + +; + +E. cochlearius +Kuang & Liu, 1991 + +; + +E. flaccidus +Fryer, 1965 + +; + +E. genuinus +( +Kokubo, 1914 +) + +; + +E. glyptothoracis +Kuang & Qian, 1983 + +; + +E. hemibagri +Zhang & Ma, 1994 + +; + +E. iraquensis +Amado, in Amado, da Rocha, Piasecki + +, Al- Daraji & Mhaisen, 2001; + +E. jiangxiensis +Liu, 1998 + +; + +E. lamellifer +Fryer, 1961 + +; + +E. leiocassi +Xu, 1987 + +; + +E. longicaudatus +Kuang & Li, 1984 + +; + +E. manicatus +Wilson, 1911 + +; + +E. mendisi +Fernando & Hanek, 1973 + +; + +E. mirabilis +Oldewage & van +As, 1987 + +; + +E. orientalis +Yamaguti, 1939 + +; + +E. pararostralis +Amado, in Amado, da Rocha, Piasecki, Al-Daraji & Mhaisen, 2001 + +; + +E. peregrinus +Heller, 1865 + +; + +E. philippinensis +Velasquez, 1951 + +; + +E. rostralis +Ho, Jayarajan & Radhakrishnan, 1992 + +; + +E. rotundicorpus +Jones & Hine, 1983 + +; + +E. shehyangensis +Wang, 1961 + +; + +E. sieboldi +von +Nordmann, 1832 + +; + +E. sittangenesis +El-Rashidy & Boxshall, 2002 + +; + +E. synanceiensis +Amado, in Amado, da Rocha, Piasecki, Al-Daraji & Mhaisen, 2001 + +; + +E. uniseriatus +Ho, Jayarajan & Radhakrishnan, 1992 + +; + +E. xenomelanirisi +Carvalho, 1955 + +and + +E. xinjiangensis +Kuang & Qian, 1985 + +. + + +This list excludes + +E. cunningtoni +Capart, 1944 + +because of uncertainty about the setation of leg 5. In the original description leg 5 was illustrated as carrying two terminal setae, but +Capart (1944: 15) +stated that this limb also had a lateral seta which was not figured - “une soie latérale (non figurée)”. Subsequently, after examining new material from the +type +locality, +Fryer (1964 +, +1965 +) raised doubts about the existence of this third seta on the free exopodal segment. Irrespective of the form of leg 5, this species differs from the new species in the possession of an outer margin spine on the second exopodal segment of leg 1, and in the form of the second endopodal segment of the antenna, which in + +E. cunningtoni + +has a marked indentation proximally on its convex outer margin, and in the very short antennary claw. + + +This assemblage of 28 species ( +Table 1 +) can be subdivided by reference to the segmentation pattern of the female antennules. Descriptions of antennule segmentation are generally reliable in the +Ergasilidae +, although details of antennulary setation are not, particularly in the older literature, because setae are easily broken or overlooked, and the aesthetascs can be difficult to see. The new species possesses a 6-segmented antennule, in common with 24 of the species listed, but the remaining four species, + +E. flaccidus +, +E. pararostralis +, +E. rostralis + +and + +E. uniseriatus + +, all exhibit a 5-segmented antennule and can be eliminated from further comparisons. + + + +TABLE 1. +Comparisons of character states exhibited by species of + +Ergasilus + +with a 3-segmented endopod of leg 1, plus 2 setae on the free exopodal segment of leg 5. Abbreviations: A1 = number of antennule segments; P2 = number of inner setae on second endopodal segment of leg 2; CR (L:W) = length to width ratio of caudal rami. + + +Species Body length A1 Antenna P2 CR (L:W) Data source +(mm) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+ +E. batai + +09–1.256slender27:1Karamchandani (1952)
+ +E. borneoensis + +0.9–1.16slender21.3:1Yamaguti (1954)
+ +E. cochlearius + +0.54–0.656slender21.5:1Kuang & Liu (1991)
+ +E. flaccidus + +0.6–0.95slender11:1Fryer (1965)
+ +E. genuinus + +0.72–0.846slender21.3:1 +Ohtsuka +et al. +(2004) +
+ +E. glyptothoracis + +0.85–1.016inflated21.2:1Kuang & Qian (1983)
+ +E. hemibagri + +0.66–0.936slender11.3:1Zhang & Ma (1994)
+ +E. iraquensis + +1.086slender11:1 +Amado +et al. +(2001) +
+ +E. jiangxiensis + +0.556slender26:1Liu (1998)
+ +E. kimi + + +sp. nov. + +0.61–0.636slender21.4:1present account
+ +E. lamellifer + +0.856lamella21.6:1Fryer (1961)
+ +E. leiocassi + +0.78–0.966slender11.1:1Xu (1987)
+ +E. longicaudatus + +0.95–0.996slender26:1Kuang & Li (1984)
+ +E. manicatus + +0.756inflated?1:1Wilson (1911)
+ +E. mendisi + +0.8–0.96slender23.5:1Fernando & Hanek (1973)
+ +E. mirabilis + +0.936slender12:1Oldewage & van As (1987)
+ +E. orientalis + +0.76inflated21.2:1Yamaguti (1939)
+ +E. pararostralis + +0.715slender11:1 +Amado +et al. +(2001) +
+ +E. peregrinus + +0.796slender21.2:1Kim & Choi (2003)
+ +E. philippinensis + +0.866slender22.7:1Velasquez (1951)
+ +E. rostralis + +0.80–0.865slender21.5:1 +Ho +et al. +(1992) +
+ +E. rotundicorpus + +0.606inflated21:1Jones & Hine (1983)
+ +E. shehyangensis + +0.91–1.156slender21.5:1Wang (1961)
+ +E. sieboldi + +1.0–2.06slender22.1:1Kabata (1979)
+ +E. sittangenesis + +0.786slender11.7:1El-Rashidy & Boxshall (2002)
+ +E. synanceiensis + +0.896slender21.3:1 +Amado +et al. +(2001) +
+ +E. uniseriatus + +0.56–0.605slender21.2:1 +Ho +et al. +(1992) +
+ +E. xenomelanirisi + +0.6–0.76slender1?1:1Carvalho (1955)
+ +E. xinjiangensis + +0.89–0.986slender23:1Kuang & Qian (1985)
+
+ +A second group of species can be separated from within the remaining 24 species by the gross morphology of the antenna, which forms the attachment apparatus securing the adult female to the gill filaments of its fish host. In + +E. glyptothoracis +, +E. manicatus +, +E. orientalis + +and + +E. rotundicorpus + +the antenna is a relatively short and compact limb, and the joint between the coxobasis and the first endopodal segment is inflated to form a distinctive lateral swelling ( +Table 1 +). In the new species and in the remaining 20 species, the antenna is a relatively slender limb and the joint between the two proximal segments is not inflated. One other species, + +E. lamellifer + +, also has a distinctive antenna. When first describing this species +Fryer (1961) +highlighted the presence of a ridge-like lamella along the margin of the first endopodal segment; indeed, this feature was sufficiently remarkable to be alluded to in the name of the species. No other species listed in +Table 1 +has a lamella along the margin of this segment. + + +The proportions of the caudal rami, as indicated by the length to width ratio (L:W), has proven a useful character for species discrimination in many different copepod families, and there are marked differences between some of the species listed in +Table 1 +. The most elongate ramus is found in + +E. batai + +in which the L:W ratio is 7:1 ( +Karamchandani 1952 +), whilst in several species the ramus is about as long as wide ( +Table 1 +). It is convenient to divide the species into two categories, those with an elongate caudal ramus ( +i.e. +, L:W ratio of 3:1 or greater) and those with a relatively short caudal ramus ( +i.e. +, a L:W ratio of less than 3:1). The elongate category includes + +E. batai + +, + +E. jiangxiensis + +, + +E. longicaudatus + +, + +E. mendisi + +and + +E. xinjiangensis + +. Elimination of species listed in +Table 1 +on the basis of gross differences in antennulary segmentation, in the form of the antenna and in the proportions of the caudal rami, leaves 14 species for comparison with the new species in greater detail. + + +Descriptions of swimming leg setation in the family +Ergasilidae +are sometimes unreliable. In + +E +. +jiangxiensis + +, for example, leg 2 and leg 4 are both described as bearing two inner setae on the second endopodal segment, while leg 3 is shown with only one seta on the equivalent segment ( +Liu 1998 +). Such a pattern is almost certainly incorrect since reductions in leg setation along the leg series in copepods typically follow an antero-posterior sequence. The original description of the legs of + +E. xenomelanirisi + +by +Carvalho (1955) +is similarly problematic, with many setae missing and spines drawn as present where spines never occur in other members of this family. Given such confusion, it is necessary to exercise caution when interpreting some of the older published descriptions of leg setation in small species. However, the recent detailed description of + +E. sittangenesis + +by +El-Rashidy & Boxshall (2002) +revealed an unusual feature of leg setation: the second endopodal segment of leg 2 has only one inner seta while this segment on each of legs 3 and 4 carries two setae. Four other species, all described relatively recently, share this unusual setation pattern, + +E. hemibagri + +, + +E. iraquensis + +, + +E. leiocassi + +and + +E. mirabilis + +. The new species differs in the possession of two setae on this segment in leg 2. All five of these species also have markedly larger body size than the new species which, with a mean body length of +0.62 mm +, is one of the smallest of those listed ( +Table 1 +). + + +The inadequate description of + +E. xenomelanirisi + +from +Brazil +( +Carvalho 1955 +) also shows a single seta on the second endopodal segment of leg 2, but none on the same segment of leg 3; further evidence that it cannot be considered accurate. For this species comparisons can be restricted to the largest and easiest limb to observe, the antenna, which provides several key differences from the new species. In + +E. xenomelanirisi + +the antennary claw is small, only about half the length of the second endopodal segment, whereas in the new species claw and segment are similar in length. The first endopodal segment is about twice as long as wide in + +E. xenomelanirisi + +, whereas in the new species it is about 4.2 times longer than wide. + + +Yamaguti (1954) +described + +E. borneoensis + +from the gills of “an unknown fish, probably of the Coridae” caught at Bandjermasin, Borneo, close to the +type +locality of the new species. The Coridae is not a valid family but the genus + +Coris +Lacepède, 1801 + +is currently included within the actinopterygian family +Labridae +. The new species can be distinguished by its smaller body size (see +Table 1 +), relatively long antennary claw ( +cf. +about 60% length of second endopodal segment in + +E. borneoensis + +), and the presence of five setal elements on the distal exopodal segment of leg 4 ( +cf. +6 in + +E. borneoensis + +). The unusual form of the mandible in + +E. borneoensis + +, with four blades, would be unique in the genus and requires confirmation. + + +Both sexes of + +E. genuinus + +were redescribed in detail by + +Ohtsuka +et al. +(2004) + +and it shares the identical leg setation pattern with the new species, but significant differences are found in the antennae. + +Ergasilus genuinus + +has a rather robust antenna with the first endopodal segment about 2.2 times longer than wide and bearing two spiniform sensillae in the distal half, whereas in the new species this segment is about 4.2 times longer than wide and carries a knob-like sensilla close to the middle of the medial margin ( +Fig. 2 +B). The interpodal plates are more heavily ornamented in + +E. genuinus + +, with spinules scattered over the entire surface of each plate, not just a single spinule row along its posterior border ( +Fig. 1 +D). + + +Kim & Choi (2003) +redescribed + +E. peregrinus + +, a widespread species reported from +China +, +Korea +and +Russia +(far eastern zone of Siberia). Again, the setation pattern is identical to that of the new species and the main differences can be found in the antennae. + +Ergasilus peregrinus + +has a robust antenna with the first endopodal segment about twice longer than wide, bearing a single sensilla in the distal third, and the second endopodal segment lacks sensillae. In contrast, the first endopodal segment is slender in the new species (about 4.2 times longer than wide) and carries a knob-like sensilla close to the middle of the medial margin, while the second segment has a prominent marginal sensilla proximally ( +Fig. 2 +B). + + + +FIGURE 1. + +Ergasilus kimi + + +sp. nov. + +(paratype adult female). A, habitus, dorsal; B, genital double-somite, free abdominal somites and caudal rami, ventral; C, rostrum, ventral; D, intercoxal sclerites of legs 1 to 3 and associated interpodal plates, ventral; E. left fifth leg, lateral. Scale bars: A = 200 µm, B–E = 50 µm. + + + + +FIGURE 2. + +Ergasilus kimi + + +sp. nov. + +(paratype adult female). A, antennule, ventral; B, antenna, lateral, with insets showing detail of sensillae on first and second endopodal segments; C, labrum, ventral; D, mandible, ventral in situ; E, maxillule, ventral in situ; F, maxilla, ventral in situ. Scale bars: A, C, F = 50 µm, B = 100 µm, D–E = 25 µm. + + + +The +type +species, + +E. sieboldi + +, is one of the largest in the genus, with a body length of between 1 and +2 mm +( +Kabata 1979 +), two to three times larger than the new species. The detailed redescription of this species by +Kabata (1979) +shows differences in leg setation: leg 1 carries an outer spine on the second exopodal segment (absent in the new species), and legs 2 and 3 each carry an outer spine on the third exopodal segment (absent in the new species). + +Ergasilus cochlearius + +(see +Kuang & Liu 1991 +) shares the same leg setation pattern as + +E. sieboldi + +, and thus also differs from the new species. In addition the antennary claw is distinctly shorter than the second endopodal segment in both + +E. sieboldi + +and + +E. cochlearius + +, but about the same length in the new species. + + + +FIGURE 3. + +Ergasilus kimi + + +sp. nov. + +(paratype adult female). A, leg 1, anterior; B, leg 2, anterior; C, leg 3, anterior; D, leg 4, anterior. Scale bar = 50 µm. + + + + +Ergasilus synaceiensis + +has the same leg setation pattern as the new species (see + +Amado +et al +. 2001 + +) but differs in having a much more swollen prosome than the new species, and its genital double-somite is just longer than wide whereas in the new species it is wider than long. In addition, the antennary claw is only half the length of the second endopodal segment in + +E. synaceiensis + +and bears two sensillae (one at mid-length, the other distally), while in the new species the claw and segment are similar in length and only a single, proximally-located sensilla is present. + + +The antenna of + +E. philippinensis + +is long and slender but the claw is only about half the length of the second endopodal segment ( +Velasquez 1951 +) whereas in the new species the claw and segment are about equal in length. The caudal rami are also more elongate in + +E. philippinensis + +than in the new species ( +Table 1 +). + + +Finally, the new species can be distinguished from + +E. shehyangensis + +(see +Wang 1961 +) by differences in the antenna and there are also apparent differences in leg setation. The antenna of + +E. shehyangensis + +has sensillae located in the distal third of the first endopodal segment and in the middle of the second, whereas in the new species the former is located mid-segment and the latter is located in the proximal third. Also the claw is only half the length of the second endopodal segment in + +E. shehyangensis + +, but about the same length in the new species. Outer spines are shown as present on the terminal exopod segment of legs 2 and 4 of + +E. shehyangensis + +by +Wang (1961) +. No such spines are present in the new species but the lack of this spine on Wang’s figure of leg 3 raises some concern over the accuracy of the description. + +
+
+
\ No newline at end of file diff --git a/data/38/23/8E/38238E0934D852AC8BAA8561EE1AF47F.xml b/data/38/23/8E/38238E0934D852AC8BAA8561EE1AF47F.xml new file mode 100644 index 00000000000..06fc2e552bc --- /dev/null +++ b/data/38/23/8E/38238E0934D852AC8BAA8561EE1AF47F.xml @@ -0,0 +1,138 @@ + + + +Exploration into the hidden world of Mozambique's sky island forests: new discoveries of reptiles and amphibians + + + +Author + +Conradie, Werner +Port Elizabeth Museum (Bayworld), P. O. Box 13147, Humewood 6013, South Africa & South African Institute for Aquatic Biodiversity, P / Bag 1015, Grahamstown, 6140, South Africa +werner@bayworld.co.za + + + +Author + +Bittencourt-Silva, Gabriela B. +University of Basel, Biogeography Research Group, Department of Environmental Sciences, Basel 4056, Switzerland + + + +Author + +Engelbrecht, Hanlie M. +South African National Biodiversity Institute, Private Bag X 7, Claremont, 7735, South Africa & Department of Botany and Zoology, Stellenbosch University, Matieland 7602, Stellenbosch, South Africa + + + +Author + +Loader, Simon P. +University of Roehampton, Department of Life Sciences, London, SW 15 4 JD, United Kingdom + + + +Author + +Menegon, Michele +MUSE, Museo delle Scienze, Viale del Lavoro e delle Scienza, 3 Trento 38122, Italy + + + +Author + +Nanvonamuquitxo, Cristovao +Faculty of Natural Sciences, Lurio University, Pemba, 958, Mozambique + + + +Author + +Scott, Michael +Khangela Safaris, www. khangelasafaris. com, Bulawayo, Zimbabwe + + + +Author + +Tolley, Krystal A. +South African National Biodiversity Institute, Private Bag X 7, Claremont, 7735, South Africa & Department of Botany and Zoology, Stellenbosch University, Matieland 7602, Stellenbosch, South Africa + +text + + +Zoosystematics and Evolution + + +2016 + +2016-09-26 + + +92 + + +2 + + +163 +180 + + + + +http://dx.doi.org/10.3897/zse.92.9948 + +journal article +http://dx.doi.org/10.3897/zse.92.9948 +1860-0743-2-163 +9DA068DAB881409199FE252D31DDC7D1 +FFCC824A3E5F060CFFF2FF83B964FFD2 +155320 + + + + + +Philothamnus hoplogaster ( +Guenther +, 1863) + + + + +Material + + +Mt. Mabu +(PEM +R21154 +, female, +390 mm +SVL +165 mm +TL), Mt. +M'paluwe +(PEM +R21219 +, male, +406 mm +SVL + 188 TL) + +. + + + +Comments + +Specimen collected from Mt. Mabu has 10 black spots anterior on the dorsum, while the Mt. +M'paluwe +specimen has uniform lime-green colouration. The Mt. Mabu specimen was collected from an overhanging tree along a well vegetated low-elevation stream at night, while the Mt. +M'paluwe +was collected around a water tank at the Oasis Water Camp. + + + + \ No newline at end of file diff --git a/data/38/24/FC/3824FC1C08FF31C38B87B2228B72DB8C.xml b/data/38/24/FC/3824FC1C08FF31C38B87B2228B72DB8C.xml new file mode 100644 index 00000000000..6f99d13759e --- /dev/null +++ b/data/38/24/FC/3824FC1C08FF31C38B87B2228B72DB8C.xml @@ -0,0 +1,94 @@ + + + +Polychaetes of Greece: an updated and annotated checklist + + + +Author + +Faulwetter, Sarah + + + +Author + +Simboura, Nomiki + + + +Author + +Katsiaras, Nikolaos + + + +Author + +Chatzigeorgiou, Giorgos + + + +Author + +Arvanitidis, Christos + +text + + +Biodiversity Data Journal + + +2017 + +5 + + +20997 +20997 + + + + +http://dx.doi.org/10.3897/BDJ.5.e20997 + +journal article +http://dx.doi.org/10.3897/BDJ.5.e20997 +1314-2828-5-20997 + + + + +Virchowia clavata Langerhans, 1879 + + + + +Umbellisyllis clavata +(Langerhans, 1879) | +Virchowia clavata +Langerhans, 1879 + + + +Notes + +Reported from Greece by +Simboura (1996) +and +Faulwetter et al. (2011a) +. In the Mediterranean also known from Spain ( + +San +Martin +2003 + +), Italy ( +Castelli et al. 2008 +) and France ( +Nygren and Pleijel 2010 +), otherwise known only from Madeira. + + + + \ No newline at end of file diff --git a/data/38/25/08/382508163B99B221679A5A926B0CE4DA.xml b/data/38/25/08/382508163B99B221679A5A926B0CE4DA.xml new file mode 100644 index 00000000000..1fecc10885b --- /dev/null +++ b/data/38/25/08/382508163B99B221679A5A926B0CE4DA.xml @@ -0,0 +1,455 @@ + + + +Annotated catalog and bibliography of the cyclocephaline scarab beetles (Coleoptera, Scarabaeidae, Dynastinae, Cyclocephalini) + + + +Author + +Moore, Matthew R. +Department of Entomology and Nematology, University of Florida, Building 1881 Natural Area Drive, Steinmetz Hall, Gainesville, FL 32611, USA +cyclocephala@gmail.com + + + +Author + +Cave, Ronald D. +Department of Entomology and Nematology, University of Florida, Indian River Research and Education Center, 2199 South Rock Road, Fort Pierce, FL 34945, USA + + + +Author + +Branham, Marc A. +Department of Entomology and Nematology, University of Florida, Building 1881 Natural Area Drive, Steinmetz Hall, Gainesville, FL 32611, USA + +text + + +ZooKeys + + +2018 + +2018-03-22 + + +745 + + +101 +378 + + + + +http://dx.doi.org/10.3897/zookeys.745.23685 + +journal article +http://dx.doi.org/10.3897/zookeys.745.23685 +1313-2970-745-101 +8785DC6BC2A244FD94B6243EB07C717F +047DFFCAFFA5F32EA97C873F4708943F +1222435 + + + + +Cyclocephala longula LeConte, 1863 + + + + +Cyclocephala longula +LeConte, 1863: 79 [original combination]. + + +Ochrosidia (Ochrosidia) longula +(LeConte) [new combination and new subgeneric classification by +Casey 1915 +: 142]. + + +Cyclocephala longula +LeConte [revised combination and removal of subgeneric classification by +Arrow 1937b +: 8, 12]. + + +syn. +Ochrosidia (Ochrosidia) abrupta +Casey, 1915: 152 [original combination]. + + +Cyclocephala abrupta +(Casey) [new combination and removal of subgeneric classification by +Arrow 1937b +: 8]. + + +Cyclocephala (Spilosota) abrupta +(Casey) [new subgeneric classification by +Saylor 1937 +: 69]. + + +Cyclocephala longula +LeConte [synonymy by +Saylor 1945 +: 384]. + + +syn. +Ochrosidia (Ochrosidia) ambiens +Casey, 1915: 155 [original combination]. + + +Cyclocephala ambiens +(Casey) [new combination and removal of subgeneric classification by +Arrow 1937b +: 8]. + + +Cyclocephala longula +LeConte [synonymy by +Saylor 1945 +: 384]. + + +syn. +Ochrosidia (Ochrosidia) rustica +Casey, 1915: 157 [original combination]. + + +Cyclocephala californica +Arrow, 1937b: 9 [original combination, new replacement name for +Cyclocephala rustica +(Casey)]. + + +Cyclocephala (Spilosota) abrupta +(Casey) [synonymy by +Saylor 1937 +: 69]. + + +Cyclocephala longula +LeConte [synonymy by +Saylor 1945 +: 384]. + + +syn. +Ochrosidia (Ochrosidia) marcida +Casey, 1915: 155 [original combination]. + + +Cyclocephala marcida +(Casey) [new combination and removal of subgeneric classification by +Arrow 1937b +, 8, 12]. + + +Cyclocephala longula +LeConte [synonymy by +Saylor 1945 +: 384]. + + +syn. +Ochrosidia (Ochrosidia) modulata +Casey, 1915: 154 [original combination]. + + +Cyclocephala modulata +(Casey) [new combination and removal of subgeneric classification by +Arrow 1937b +: 8, 13]. + + +Cyclocephala longula +LeConte [synonymy by +Saylor 1945 +: 384]. + + +syn. +Ochrosidia (Ochrosidia) obesula +Casey, 1915: 156 [original combination]. + + +Cyclocephala obesula +(Casey) [new combination by +Arrow 1937b +: 8, 13]. + + +Cyclocephala (Spilosota) abrupta +(Casey) [synonymy by +Saylor 1937 +: 69]. + + +Cyclocephala longula +LeConte [synonymy by +Saylor 1945 +: 384]. + + +syn. +Ochrosidia (Ochrosidia) oblongula +Casey, 1915: 156 [original combination]. + + +Cyclocephala oblongula +(Casey) [new combination and removal of subgeneric classification by +Arrow 1937b +: 8, 13]. + + +Cyclocephala (Spilosota) abrupta +(Case) [synonymy by +Saylor 1937 +: 69]. + + +syn. +Ochrosidia (Ochrosidia) phasma +Casey, 1915: 153 [original combination]. + + +Cyclocephala phasma +(Casey) [new combination and removal of subgeneric classification by +Arrow 1937b +: 8, 14]. + + +Cyclocephala (Spilosota) abrupta +(Casey) [synonymy by +Saylor 1937 +: 69]. + + +syn. +Ochrosidia (Ochrosidia) prona +Casey, 1915: 157 [original combination]. + + +Cyclocephala prona +(Casey) [new combination and removal of subgeneric classification by +Arrow 1937b +: 8, 14]. + + +Cyclocephala longula +LeConte [synonymy by +Saylor 1945 +: 384]. + + +syn. +Ochrosidia (Ochrosidia) reflexa +Casey, 1915: 153 [original combination]. + + +Cyclocephala reflexa +(Casey) [new combination and removal of subgeneric classification by +Arrow 1937b +: 8, 15]. + + +Cyclocephala (Spilosota) abrupta +(Casey) [synonymy by +Saylor 1937 +: 69]. + + +syn. +Ochrosidia (Ochrosidia) rugulifrons +Casey, 1915: 154 [original combination]. + + +Cyclocephala rugulifrons +(Casey) [new combination and removal of subgeneric classification by +Arrow 1937b +: 8, 15]. + + +Cyclocephala longula +LeConte [synonymy by +Saylor 1945 +: 384]. + + + +Types. + +Type of + +C. longula + +at MCZ ( + +Endrodi +1966 + +). Types of the Casey synonyms are at USNM ( + +Endrodi +1966 + +). + + + +Distribution. +CANADA: British Columbia. MEXICO: Baja California, Baja California Sur, Chihuahua, Sonora. UNITED STATES: Arizona, California, Colorado, Idaho, Illinois, Kansas, Montana, Nebraska, Nevada, New Mexico, Oklahoma, Oregon, South Dakota, Texas, Utah, Washington, Wyoming. + + +References. + +LeConte 1863 +, +Gerstaecker 1865 +, +Crotch 1873 +, +Henshaw 1885 +, +Horn 1894 +, +Wickham 1896 +, +Fall 1901 +, +Casey 1915 +, +Leng 1920 +, +Dawson 1922 +, +Arrow 1937b +, +Moore 1937 +, +Blackwelder 1939 +, +1944 +, +Riegel 1942b +, +Saylor 1937 +, +1945 +, +1948 +, +Blackwelder and Blackwelder 1948 +, +Allred and Beck 1965 +, +Ritcher 1966 +, + +Howden and +Endrodi +1966 + +, +Arnett 1968 +, +Pike et al. 1976 +, + +Endrodi +1966 + +, +1969b +, +1985a +, +Hatch 1971 +, +Kirk and Balsbaugh 1975 +, +Bechtel et al. 1983 +, +Hardy 1991 +, +McNamara 1991 +, +Ratcliffe 1991 +, +Poole and Gentili 1996 +, + +Ratcliffe and +Moron +1997 + +, +Bauernfeind et al. 1999 +, +Bauernfeind 2001 +, +Riley and Wolfe 2003 +, +Ratcliffe and Paulsen 2008 +, +Smith 2003 +, +2009 +, +Krajcik 2005 +, +2012 +, +Haviland and Hernandez 2012 +, +Bousquet et al. 2013 +, +Breeschoten et al. 2013 +, +Ratcliffe et al. 2013 +, +Ratcliffe and Cave 2017 +. + + + +Remarks. + + +Cyclocephala longula + +was reported from Wisconsin and Florida (USA) ( + +Endrodi +1966 + +, +1985a +). These records are likely based on misidentifications ( +Ratcliffe and Paulsen 2008 +). Additionally, + +C. longula + +was reported from Nicaragua (Boaco and Managua) ( +Maes 1987 +, +1994 +). The validity of these records is uncertain as faunistic studies focused on Nicaragua did not report additional specimens of + +C. longula + +( +Ratcliffe and Cave 2006 +). + + + + \ No newline at end of file diff --git a/data/38/25/0F/38250F35C9796329FF32FC318E16FE52.xml b/data/38/25/0F/38250F35C9796329FF32FC318E16FE52.xml new file mode 100644 index 00000000000..8fddd3c85e2 --- /dev/null +++ b/data/38/25/0F/38250F35C9796329FF32FC318E16FE52.xml @@ -0,0 +1,316 @@ + + + +Tripogon sugathakumariae (Poaceae: Chloridoideae: Tripogoninae): a new species from southern Western Ghats, Kerala, India + + + +Author + +Jabeena, Manjakulam Khadhersha +0000-0003-1687-8785 +Post Graduate and Research Department of Botany, Govt. Victoria College (University of Calicut), Palakkad, Kerala, PIN 678001, India. & jabeena 1993 @ gmail. com; https: // orcid. org / 0000 - 0003 - 1687 - 8785 +jabeena1993@gmail.com + + + +Author + +Prabhukumar, Konickal Mambetta +PDSH Division, CSIR-National Botanical Research Institute, Rana Pratap Marg, Lucknow, PIN 226001, Uttar Pradesh. & prabhumkrishna @ gmail. com; https: // orcid. org / 0000 - 0003 - 3341 - 27175 +prabhumkrishna@gmail.com + + + +Author + +Remya, Sivakumaran +0000-0002-2402-6382 +Post Graduate and Research Department of Botany, Govt. Victoria College (University of Calicut), Palakkad, Kerala, PIN 678001, India. & remyasivakumaran @ gmail. com; https: // orcid. org / 0000 - 0002 - 2402 - 6382 +remyasivakumaran@gmail.com + + + +Author + +Athira, Subramanian +0000-0003-4740-6596 +Post Graduate and Research Department of Botany, Govt. Victoria College (University of Calicut), Palakkad, Kerala, PIN 678001, India. & athirasub 96 @ gmail. com; https: // orcid. org / 0000 - 0003 - 4740 - 6596 +athirasub96@gmail.com + + + +Author + +Hareesh, Vadakkoot Sankaran +0000-0001-5474-277X +Malabar Botanical Garden & Institute of Plant Sciences, Olavanna, Kozhikkode. & hareeshhariz @ gmail. com; https: // orcid. org / 0000 - 0001 - 5474 - 277 X +hareeshhariz@gmail.com + + + +Author + +Maya, Chandrasekharan Nair +0000-0002-1667-817X +Post Graduate and Research Department of Botany, Govt. Victoria College (University of Calicut), Palakkad, Kerala, PIN 678001, India. & drmayadhoni @ gmail. com; https: // orcid. org / 0000 - 0002 - 1667 - 817 X +drmayadhoni@gmail.com + + + +Author + +Sunil, Chandrasseril Narayanan +0000-0003-3124-617X +Department of Botany, S. N. M. College, Maliankara, Kerala, PIN 683516, India. & drcnsunilsnamc @ gmail. com; https: // orcid. org / 0000 - 0003 - 3124 - 617 X +drcnsunilsnamc@gmail.com + +text + + +Phytotaxa + + +2022 + +2022-02-22 + + +536 + + +1 + + +101 +105 + + + +journal article +20518 +10.11646/phytotaxa.536.1.7 +c6b17dd2-422d-4762-bf52-2140c6effeb5 +1179-3163 +6252849 + + + + + +Tripogon sugathakumariae +Jabeena, Sunil & Maya + + +sp. nov. + +( +Figs.1 +& +2 +). + + + + +Type: +— + +INDIA +: +Kerala +: +Palakkad district +, +Nelliyampathy +hills, +Mattumala +, +10°30’10”N +, +76°42’17”E +, + +1170 m + +, + +19 November 2020 + +, + +Jabeena M.K. +& +Maya C. Nair + +4380 ( +holotype +: MH; isotypes: CALI, LWG, CAL) + +. + + + + +Diagnosis: +—The new species is similar to + +T.bromoides + +in the presence of glabrous nodes, hairy leaf blades, glabrous peduncle, single awned upper glume, and 3-awned lemma, but differs in having distinct eciliate membraneous ligule fringed with long hairs at the ends of leaf sheath (vs. indistinct ligule with a tuft of +1–2 mm +long hairs at apex), leaf blade 4.0– +17 cm +long (vs. +15–50 cm +long), spikelets 1.0– +1.5 mm +broad, straw-coloured (vs. +2–2.8 mm +broad, olive-green or yellowish with a purple tinge), unidentate awned upper glume (vs. bidentate upper glume with or without awn), lemma 3-lobed and 3-awned without a definite lobe between the median and lateral awns (vs. 4-lobed and 3-awned, with a distinct lobe between the median and lateral awns) and median awn equal or slightly longer than lemma (vs. shorter than lemma). + + + + +Description: +—Caespitose perennials. Basal sheaths persistent with remnants of culm bases of previous years, not splitting into fibrous threads. Culms +10–20 cm +tall, terete, erect; nodes glabrous, slightly geniculate. Leaf blades 4.0– 17× +0.1–0.3 cm +, linear-lanceolate, flat, margins entire, acuminate at apex, sparsely villous on both sides, more hairy towards base; hairs bulbous based, 1.5–2.0 mm long; leaf sheaths 1.0– +4.5 cm +long; ligules membraneous, eciliate, fringed with long hairs at the ends of leaf sheath. Inflorescence solitary, terminal, spiciform raceme, 6.0– +12 cm +long, with 18–52 spikelets alternately arranged along both sides of raceme; peduncle stout, +2–5 cm +long, glabrous; rachis 2.5–4.0 mm long, glabrous. Spikelets 4–7-flowered, secund, imbricate, 4–8×1.0– +1.5 mm +, lanceolate, dorsi-ventrally flattened, straw-coloured; callus bearded, hairs +0.3–0.5 mm +long; rachilla 0.8–1.0 mm long, smooth. Lower glume 1.8–2.5× +0.8–1mm +, oblong-lanceolate, asymmetrical, broadened on one side, 1-veined, acuminate to mucronulate at apex, mucro ca. +0.2 mm +long, scabridulose. Upper glume 4.3–5.5×0.8–1.0 mm (including awn), elliptic-lanceolate, symmetrical, 1-veined, 1-awned; awn ca. +1mm +long, contiguous with the apex. Lemma 2.3–2.8× +1.1–1.3 mm +, ovatelanceolate, sub-coriaceous, 3-veined, 3-lobed at apex, without lobes between the median and lateral awns, the mid-lobe acute at apex or rarely with a minute notch in the lowermost lemma, 3-awned; awns scabridulose; central awn +2.3–3.2 mm +long, a little longer or about equaling with its lemma; lateral awns +1–1.5 mm +long, about half the length of median awn. Palea 1.5–2.3×0.7–1.0 mm, elliptic-oblanceolate, notched at apex, hyaline, 2-veined, 2-keeled; keels scabrid along the margins from above the middle, minutely winged. Lodicules 2, +0.3–0.4 mm +long, wedge shaped, glabrous. Stamens 3; anthers +0.8–1 mm +long, oblong, yellow; filaments +0.75 mm +long, slender, glabrous. Ovary +0.4–0.5 mm +long, obovate, glabrous; styles 2, +0.5–0.7 mm +long, slender, hyaline; stigma +1–1.5 mm +long, feathery. Caryopsis not seen. + + + + +Phenology: +—August-December. + + + + +FIGURE 1. + +Tripogon sugathakumariae +A. Habitat. B. & C. Habit. D. Portion + +of raceme. E. Single spikelet. F. A portion of spikelet showing callus hairs. G. Rachilla. H. Upper glume. I. Lower glume. J. Palea. K. Lemma. L. Stamen. M. Pistil. (Photos: Jabeena M. K. and Remya S.) + + + + +FIGURE 2. + +Tripogon sugathakumariae +A. Habit. B. Portion + +of raceme. C. Spikelet. D. A portion of spikelet showing callus hairs. E. Rachilla. F. Upper glume. G. Lower glume. H. Lemma. I. Palea. J. Stamen. K. Stamens and Pistil L. Pistil.(Illustrated by Jabeena M. K. from Jabeena M. K. & Maya C. Nair 4380) + + + + +Etymology: +—The specific epithet is named after the renowned writer in Malayalam poetry, who stood with her strong words for mother Nature and conservation of natural resources, Padmasree Smt. Sugathakumari. She was at the forefront of environmental and feminist movements in +Kerala +and played a prominent role in the save Silent Valley movement. + + + + +Distribution and ecology: +—So far, the new species is collected only from the +type +locality of Mattumala, in Nelliyampathy hills of +Kerala +at an elevation of +1100–1200 m +a.s.l. + +Tripogon sugathakumariae + +was found growing in open montane grasslands along with + +T. bromoides +Roemer & Schultes + +and + +Alysicarpus bupleurifolius +( +Linnaeus 1753: 745 +) De +Candolle (1825: 352) + +. + + + + +Additional specimens examined: +— + +INDIA +: +Kerala +: +Palakkad district +, +Nelliyampathy +hills, +Mattumala +, +10°30’10”N +, +76°42’17”E +, + +1170 m + +, + +19 November 2020 + +, + +C.N. Sunil + +4869 (SNMH) + +. + + + + \ No newline at end of file diff --git a/data/38/25/15/382515045573FE837CCA48C1331CFEAC.xml b/data/38/25/15/382515045573FE837CCA48C1331CFEAC.xml new file mode 100644 index 00000000000..36177a95d0c --- /dev/null +++ b/data/38/25/15/382515045573FE837CCA48C1331CFEAC.xml @@ -0,0 +1,256 @@ + + + +Order Chiroptera - Family Vespertilionidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +451 +529 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + +Vespertilionini Gray 1821 + + + + + + +Vespertilionini +Gray 1821 + +, +London Med. Repos., 15: 299 + +. + + + + +Genera: +14 genera with 81 species: + + +Genus + +Chalinolobus +Peters 1866 + +(7 species with 2 subspecies) + + +Genus + +Eudiscopus +Conisbee 1953 + +(1 species) + + +Genus + +Falsistrellus +Troughton 1943 + +(5 species) + + +Genus + +Glauconycteris +Dobson 1875 + +(12 species with 2 subspecies) + + +Genus + +Histiotus +Gervais 1856 + +(7 species with 3 subspecies) + + +Genus + +Hypsugo +Kolenati 1856 + +(18 species with 4 subspecies) + + +Genus + +Ia +Thomas 1902 + +(1 species) + + +Genus + +Laephotis +Thomas 1901 + +(4 species) + + +Genus + +Mimetillus +Thomas 1904 + +(1 species with 2 subspecies) + + +Genus + +Neoromicia +Roberts 1926 + +(11 species with 23 subspecies) + + +Genus + +Philetor +Thomas 1902 + +(1 species) + + +Genus + +Tylonycteris +Peters 1872 + +(2 species with 7 subspecies) + + +Genus + +Vespadelus +Troughton 1943 + +(9 species) + + +Genus + +Vespertilio +Linnaeus 1758 + +(2 species with 7 subspecies) + + + + +Discussion: +Does not include + +Arielulus + +, + +Eptesicus + +, + +Hesperoptenus + +, + +Glischropus + +, + +Nyctalus + +, + +Pipistrellus + +, and + +Scotozous + +; see +Volleth (1992) +, +Volleth and Heller (1994) +, and +Volleth et al. (2001) +. Includes + +Hypsugo + +, + +Falsistrellus + +, + +Tylonycteris + +, and + +Vespadelus + +; see +Volleth and Tidemann (1991) +and +Volleth and Heller (1994) +. Includes + +Neoromicia + +; see +Volleth et al. (2001) +. May include + +Nyctophilus +(Volleth and Tideman, 1991) + +, here placed in a separate tribe +Nyctophilini +along with + +Pharotis + +. + + + + \ No newline at end of file diff --git a/data/38/25/50/382550E6C36552F398D67FB4B24F4F81.xml b/data/38/25/50/382550E6C36552F398D67FB4B24F4F81.xml new file mode 100644 index 00000000000..454a7132b87 --- /dev/null +++ b/data/38/25/50/382550E6C36552F398D67FB4B24F4F81.xml @@ -0,0 +1,107 @@ + + + +Molecular phylogenetics of cool-season grasses in the subtribes Agrostidinae, Anthoxanthinae, Aveninae, Brizinae, Calothecinae, Koeleriinae and Phalaridinae (Poaceae, Pooideae, Poeae, Poeae chloroplast group 1) + + + +Author + +Saarela, Jeffery M. +Botany Section, Research and Collections, Canadian Museum of Nature, Ottawa, Ontario, Canada +jsaarela@mus-nature.ca + + + +Author + +Bull, Roger D. +Botany Section, Research and Collections, Canadian Museum of Nature, Ottawa, Ontario, Canada + + + +Author + +Paradis, Michel J. +Botany Section, Research and Collections, Canadian Museum of Nature, Ottawa, Ontario, Canada + + + +Author + +Ebata, Sharon N. +Botany Section, Research and Collections, Canadian Museum of Nature, Ottawa, Ontario, Canada + + + +Author + +Paul M. Peterson, +Department of Botany, National Museum of Natural History, Smithsonian Institution, Washington, DC, United States of America + + + +Author + +Soreng, Robert J. +Department of Botany, National Museum of Natural History, Smithsonian Institution, Washington, DC, United States of America + + + +Author + +Paszko, Beata +Department of Vascular Plant Systematics and Phytogeography, W. Szafer Institute of Botany, Polish Academy of Sciences, Krakow, Poland + +text + + +PhytoKeys + + +2017 + +2017-10-09 + + +87 + + +1 +139 + + + + +http://dx.doi.org/10.3897/phytokeys.87.12774 + +journal article +http://dx.doi.org/10.3897/phytokeys.87.12774 +1314-2003-87-1 +6960C940FFA73F60FFA87436FF86811D +1137949 + + + + + +Deschampsia +eminens var. inclusa ( +Rugolo +) Saarela + +comb. nov. + + + +Basionym. + +Deyeuxia eminens var. inclusa +Rugolo +, Darwiniana 44(1): 195, f. 24. 2006. Type: Argentina. San Juan: Dpto. Iglesia, Qda. del Agua Negra, 3750 m., 21 Feb 1979, +Cabrera 30062 +(holotype: SI). + + + + \ No newline at end of file diff --git a/data/38/25/7A/38257AF9E47B5B0C848E2F809CA91057.xml b/data/38/25/7A/38257AF9E47B5B0C848E2F809CA91057.xml new file mode 100644 index 00000000000..43cf4b14cc7 --- /dev/null +++ b/data/38/25/7A/38257AF9E47B5B0C848E2F809CA91057.xml @@ -0,0 +1,122 @@ + + + +An updated checklist of the marine fish fauna of Redang Islands, Malaysia + + + +Author + +Du, Jianguo + + + +Author + +Loh, Kar-Hoe + + + +Author + +Hu, Wenjia + + + +Author + +Zheng, Xinqing + + + +Author + +Affendi, Yang Amri + + + +Author + +Ooi, Jillian Lean Sim + + + +Author + +Ma, Zhiyuan + + + +Author + +Rizman-Idid, Mohammed + + + +Author + +Chan, Albert Apollo + +text + + +Biodiversity Data Journal + + +2019 + +7 + + +47537 +47537 + + + + +http://dx.doi.org/10.3897/BDJ.7.e47537 + +journal article +http://dx.doi.org/10.3897/BDJ.7.e47537 +1314-2828-7-e47537 +F940F7FD0A3541E98BDD33F83C2369D5 +AE1BE74780565E8D9B3522053F3B0983 + + + + +Lutjanus vitta (Quoy & Gaimard, 1824) + + + +Materials + + +Type status: +Other material +. +Occurrence: +occurrenceID: BDJ_12482_171; +Location: +country: +Malaysia +; locality: +Redang islands +; +Identification: +identifiedBy: +Loh KH and Du Jianguo + + + + +Notes + +Harborne et al. 2000 +; +Yusuf et al. 2001 +; This study. + + + + \ No newline at end of file diff --git a/data/38/25/ED/3825ED256DB8841ED44CAA19A7F26DE7.xml b/data/38/25/ED/3825ED256DB8841ED44CAA19A7F26DE7.xml new file mode 100644 index 00000000000..f28180041d4 --- /dev/null +++ b/data/38/25/ED/3825ED256DB8841ED44CAA19A7F26DE7.xml @@ -0,0 +1,77 @@ + + + +Additions to the knowledge of the land snails of Sabah (Malaysia, Borneo), including 48 new species + + + +Author + +Vermeulen, Jaap J. + + + +Author + +Liew, Thor-Seng + + + +Author + +Schilthuizen, Menno + +text + + +ZooKeys + + +2015 + +531 + + +1 +139 + + + + +http://dx.doi.org/10.3897/zookeys.531.6097 + +journal article +http://dx.doi.org/10.3897/zookeys.531.6097 +1313-2970-531-1 +C845838EC9124BD8AB4E07980F91959E +C845838EC9124BD8AB4E07980F91959E + + + + +Taxon +classification Animalia Stylommatophora Subulinidae + + + + +Family +SUBULINIDAE Fischer & Crosse + + + +Short description. + +Snails. Shell small to very large, dextral (rarely sinistral), narrowly conical to cylindrical and more or less tapering towards the apex. Sculpture absent, or inconspicuous, radial riblets with usually subordinate spiral striation; rarely spiral keels present. Aperture without teeth or lamellae, peristome thin, not reflected. Umbilicus closed or open, narrow (Family description adapted from on +Abbott 1989 +; +Herbert and Kilburn 2004 +). + + + +Habitat and distribution. +Scavengers of soil and litter. Globally distributed in the tropics and subtropics. + + + \ No newline at end of file diff --git a/data/38/25/F4/3825F43285F95D3193D225B808785798.xml b/data/38/25/F4/3825F43285F95D3193D225B808785798.xml new file mode 100644 index 00000000000..3946549539e --- /dev/null +++ b/data/38/25/F4/3825F43285F95D3193D225B808785798.xml @@ -0,0 +1,86 @@ + + + +New subgenera and species of Agraeciini (Orthoptera, Tettigoniidae, Conocephalinae) from South Asia found in historical insect collections + + + +Author + +Ingrisch, Sigfrid +https://orcid.org/0000-0002-8624-0472 +Zoologisches Forschungsmuseum Alexander Koenig, Adenauerallee 160, D- 53113 Bonn, Germany. +s.ingrisch@leibniz-zfmk.de + +text + + +Evolutionary Systematics + + +2020 + +2020-12-15 + + +4 + + +2 + + +119 +132 + + + + +http://dx.doi.org/10.3897/evolsyst.4.60525 + +journal article +http://dx.doi.org/10.3897/evolsyst.4.60525 +2535-0730-2-119 +8BD62DBF438C46508C4037C837FD573F +6301B37BBB7D51A185FB132ED24E4E81 + + + + +Liara Redtenbacher, 1891 + + + + +Liara +Redtenbacher, 1891: 444; type species +Liara rufescens +Redtenbacher, 1891: 444. + + + +Note. + +The genus contained so far three subgenera: + +Liara + +, + +Acanthocoryphus + +Karny, 1907, and + +Unalianus + +Kocak +& Kemal, 2009 (replacement name for + +Oxystethus + +Redtenbacher, 1891 because of homonymy) ( +Cigliano et al. 2020 +). In this publication a fourth subgenus and two new species are described. + + + + \ No newline at end of file diff --git a/data/38/26/1B/38261B44764FD071B4C008F26333616D.xml b/data/38/26/1B/38261B44764FD071B4C008F26333616D.xml new file mode 100644 index 00000000000..2aa7aa222a0 --- /dev/null +++ b/data/38/26/1B/38261B44764FD071B4C008F26333616D.xml @@ -0,0 +1,131 @@ + + + +A systematic revision of Baconia Lewis (Coleoptera, Histeridae, Exosternini) + + + +Author + +Caterino, Michael S. + + + +Author + +Tishechkin, Alexey K. + +text + + +ZooKeys + + +2013 + +343 + + +1 +297 + + + + +http://dx.doi.org/10.3897/zookeys.343.5744 + +journal article +http://dx.doi.org/10.3897/zookeys.343.5744 +1313-2970-343-1 + + + + +Baconia maculata +sp. n. +Figs 15 +D-F +, H, +K-L +16AMap 5 + + + +Type locality. + +ECUADOR: Orellana:Res. Ethnica Waorani [ +0.67°N +, +76.43°W +]. + + + +Type material. + +Holotype male: "ECUADOR: Depto. Orellana:Res. Ethnica Waorani, 1km S Onkone Gare Camp, Trans. Ent., +0°39'10"S +, +76°26'W +, 220m, 25 June 1996, T.L. Erwin et al. collectors" / "Insecticidal fogging of mostly bare green leaves, some with covering of lichenous or bryophytic plants in terra firme forest. Project MAXUS Lot 1536 Trans. 2 Sta. 6" / "Caterino/Tishechkin Exosternini Voucher EXO-00448" (USNM). Paratype (1): FRENCH GUIANA: +Belvedere +de +Sauel +, point de vue. +3°1'22"N +, +53°12'34"W +, FIT, 17.i.2011. SEAG leg. (CHND). + + + +Diagnostic description. + +Length: 1.7-1.8mm, width: 1.2-1.3mm; body elongate oval, subdepressed, glabrous; head and pronotum metallic greenish-blue, elytra metallic blue with distinct rufescent maculations extending across middle of disc from approximately sutural stria laterad to margin; frons together with epistoma strongly convex, weakly depressed at middle, uniformly coarsely punctate, interocular margins very weakly convergent dorsad, frontal stria present along inner margin of eyes, interrupted above antennal bases and at middle; antennal scape short, apex obliquely truncate, club elongate, subquadrate; epistoma convex along apical margin, weakly emarginate; labrum about 4 +xwider +than long, apex broadly, shallowly emarginate; mandibles +short +, each with small, acute basal tooth; palpomeres stout, flattened; pronotal sides subparallel in basal half, weakly arcuate to apex, marginal stria complete around lateral and anterior margins, submarginal stria present close to lateral marginal, ending about one-fifth from anterior corner; pronotal disk with fine ground punctation and slightly coarser secondary punctures more or less uniformly dispersed throughout; elytra with two complete epipleural striae, outer subhumeral stria absent, inner subhumeral stria present in basal two-thirds, but interrupted in middle, dorsal striae 1-5 complete to base, progressively more abbreviated apically mediad, with 5th stria obsolete in apical fourth, sutural stria present in apical two-thirds, obsolete at base; elytral disk with secondary punctures in apical fourth; prosternal keel narrow, weakly convex, base trun +cate +, carinal striae complete, bent mediad at apices, but ending freely; prosternal lobe about two-thirds keel length, broadly rounded, marginal stria slightly fragmented at sides; anterior edge of mesoventrite weakly sinuate, marginal stria complete; mesometaventral stria arched forward, crenulate, detached at sides, inner lateral metaventral stria originating close to mesocoxa, extending posterolaterad toward middle of metacoxa, outer lateral metaventral stria short, oblique, metaventral and 1st abdominal disks impunctate at middle; abdominal ventrite 1 with complete inner lateral stria and posterior fragments of outer stria; protibia with five marginal denticles, the basal two weak, outer margin serrulate between; mesotibia with 2-3 marginal spines; outer metatibial margin smooth; propygidium without transverse basal stria, with moderately large, ocellate punctures uniformly separated by about their diameters; propygidial gland openings evident about one-third from anterior and one-fourth from lateral margins; pygidium with fine, sparse ground punctation denser in apical half, with sparse secondary punctures principally in basal half. Male genitalia (Figs 15 +D-F +, H, +K-L +): T8 distinctly shorter than broad, sides subparallel, basal emargination broad, apical emargination narrow, shallow, with ventrolateral apodemes separated by about two-thirds maximum T8 width, extending about two-thirds distad beneath; S8 divided, short, inner margins approximate at base, strongly divergent to apex, bearing conspicuous fringe of setae along apical one-third, outer margins subparallel, to weakly divergent, apical guides well developed in apical half, apices broadly rounded; T9 with basal apodemes thin, about one-half total length, T9 apices narrow, bluntly subacute, weakly opposed, glabrous, ventrolateral apodemes moderately strongly projecting beneath; S9 very weakly widened in basal two-thirds, desclerotized along midline, head broad, with apicolateral points short, subparallel; tegmen with sides broadly rounded in basal half, weakly narrowed to apex, dorsal surface near base narrowly, transversely impressed, dorsobasal edge weakly arcuate, tegmen weakly sinuate in lateral aspect; median lobe broad, about two-thirds tegmen length, bearing conspicuous fine denticles on dorsal surface; basal piece nearly one-half tegmen length. + + + +Figure 16. +Baconia godmani +group. A Dorsal habitus of +Baconia maculata +B Dorsal habitus of +Baconia deliberata +C Ventral habitus of +Baconia deliberata +D Pygidia of +Baconia deliberata +E Dorsal habitus of +Baconia excelsa +F Dorsal habitus of lectotype of +Baconia violacea +. + + + + +Remarks. + +While this +species' +male genitalia associates it clearly with the +Baconia godmani +group, in external characters it is highly distinctive, with its narrow elongate body form and red-maculate elytra (Fig. 16A). + + + +Etymology. +This species is named for its distinctive elytral maculations. + + + \ No newline at end of file diff --git a/data/38/26/EE/3826EE2DFA05FFF597EB7E08FD465155.xml b/data/38/26/EE/3826EE2DFA05FFF597EB7E08FD465155.xml new file mode 100644 index 00000000000..236e5f35e8f --- /dev/null +++ b/data/38/26/EE/3826EE2DFA05FFF597EB7E08FD465155.xml @@ -0,0 +1,390 @@ + + + +Plinia delicata (Myrtaceae), a new species from southeastern Brazil + + + +Author + +Antunes, Kelly + + + +Author + +Salimena, Fátima Regina Gonçalves + + + +Author + +Sobral, Marcos + +text + + +Phytotaxa + + +2013 + +2013-09-13 + + +131 + + +1 + + +45 +48 + + + + +http://dx.doi.org/10.11646/phytotaxa.131.1.8 + +journal article +10.11646/phytotaxa.131.1.8 +1179-3163 +5085991 + + + + + + +Plinia delicata +Antunes, Salimena & Sobral + +, + +sp. nov. + +, +Fig. 1 A–G + + + + + + +Type +:— +BRAZIL +. +Minas Gerais +: +Rio Preto +, +Serra Negra +, trilha para o + +Burro +de Ouro + +, +21° 58’11” S +, +43° 53’21” W +, + +1400 m + +, + +10 Apr. 2007 + +, + +K. Antunes +248, +N.L. Abreu +, +P.L. Viana +, F.S. +Souza +, + +N.F. +O. Mota + +, +T + + +. + + +E. Almeida +, +A.M. Teles +& +B. Nordenstam + +( +holotype +CESJ, istotypes +HUFSJ +, RB, +R +) + +. + + +This species is related to + +Plinia pseudodichasiantha +, + +from which it is distinguished through its smaller inflorescences and leaves. + + + +FIGURE1. +A–G: + +Plinia delicata + +(from the holotype) 1: A. General view of branch; B. Leaves; C. Longitudinal section of flower; D. Bracteole; E. Cross section of ovary; F. Flower bud; G. Fruit. (Illustrator: +L. Menini Neto +). + + + +Shrubs to trees + +1.5– +4 m + +. Twigs glabrous, sericeous when young, with brown or grey trichomes. Leaves with petioles 1–3 × +0.8–1 mm +, sericeous, with simple trichomes to +0.3 mm +; blades discolored, brown when dry, lighter abaxially, elliptic to lanceolate or ovate, 9–35 × +5–12 mm +, 1.6–3.3 times longer than wide, glabrous or with scattered asymmetrical dibrachiate trichomes to +0.5 mm +on the abaxial surface of adult leaves, the young ones sericeous on both faces; base cuneate; apex acute; midvein adaxially sulcate and abaxially prominent; lateral veins 8 to 15 at each side, adaxially plain and inconspicuous, abaxially inconspicuous or slightly prominent; marginal vein +0.5–0.6 mm +form the +revolute margin. Inflorescences axillary, racemiform, 7–25 × +0.5 mm +, with up to five flowers; flowers sessile or with pedicels to 2 × +0.3 mm +; bracts lanceolate or linear, 1.5–5 × +0.5–0.8 mm +, glabrous or ciliate, deciduous; bracteoles lanceolate, 1–4 × +0.3–0.5 mm +, lanate or fimbriate, deciduous at anthesis, sometimes with colleters as the petioles; flower buds pyriform, 3–5 × +2–3 mm +, lanate-sericeous; calyx lobes four, 1-2 × +1-2 mm +, triangular, densely pilose on both sides, strongly reflexed at anthesis; petals elliptic or rounded, glabrous, to 2 × +2 mm +; stamens about 100, 2– +2.5 mm +, the anthers globose, +0.2–0.3 mm +in diameter, with one apical gland; staminal ring to +3 mm +in diameter, glabrous or with scattered white trichomes to +0.2 mm +; calyx tube +0.5 mm +deep; style to +3.5 mm +, the stigma punctiform; ovary with two locules and two ovules per locule. Fruits globose, +4–7 mm +in diameter, with sparse sericeous trichomes, crowned by the reflexed calyx lobes; seeds one or two per fruit, very immature in the material examined, globose or slightly reniform, the testa brown, somewhat adhered to the endocarp but easily detachable from it; embryo with two distinct cotyledons and apparently no hypocotyl. + + + + +Distribution, habitat and phenology: +—this species was collected in rainforests at the locality of Serra Negra, in the municipality of Rio Preto, which is in the southern part of the state of +Minas Gerais +, and in the natural reserve of Rio das Pedras, in the municipality of Mangaratiba, which is in the state of +Rio de Janeiro +. It was collected in rocky outcrops from +1,050 to 1,400 m +elev.; flowers were collected from January to May, and fruits were collected in April. + + +Affinities: +—this species is related to + +Plinia pseudodichasiantha +(Kiaersk.) G.M.Barroso ex Sobral + +(for description see +Kiaerskou 1893 +, under + +Eugenia pseudodichasiantha + +), a species from the Atlantic rainforests from +Rio de Janeiro +and +Espírito Santo +, from which it can be distinguished through the following characters: + + + + + + + +1. Blades 50–85 × +20–25 mm +. with 20 or more lateral veins; bracteoles to +1 mm +; plants from the interior of rainforests. ............................................................................................................................................ + +Plinia pseudodichasiantha + + + + + +-. Blades 9–35 × +5–12 mm +, with up to 15 lateral veins; bracteoles to +4 mm +; plants from rocky outcrops ....................... ................................................................................................................................................................ + +Plinia delicata + + + + + + + + +Etymology:— +the epithet is derived from the Latin word for "delicate", alluding to the small leaves of the species. + + + + +Paratypes +: + +— +BRAZIL +. +Minas Gerais +: +Rio Preto +, +Serra Negra +, trilha para o +Burro de Ouro +, + +21 Apr. 2005 + +, + +K. Antunes +et al. 162 + +( +CESJ +) + +; + +idem, + +22 Apr. 2005 + +, + +K. Antunes +et al. + +172 ( +CESJ +) + +; + +idem, 26 +Febr. +2006, + +P.L. Viana +& +N.F. Mota +1924 + +( +BHCB +, +CESJ +) + +; + +idem, + +20 May 2006 + +, + +P.L.Viana +et al. 2037 + +( +BHCB +, +CESJ +) + +; + +idem, + +10 Apr. 2007 + +, + +K. Antunes +et al. 243 + +( +CESJ +) + +. + +Rio de Janeiro +: +Mangaratiba +, +Reserva Ecológica Rio +das +Pedras +, + +18 Jan. 2001 + +, + +J.M.A. Braga +et al. 6620 + +( +RUSU +, RB) + +. + + + + \ No newline at end of file diff --git a/data/38/27/05/382705FE8AE156A7999C1D632CDF793E.xml b/data/38/27/05/382705FE8AE156A7999C1D632CDF793E.xml new file mode 100644 index 00000000000..bb4260b6974 --- /dev/null +++ b/data/38/27/05/382705FE8AE156A7999C1D632CDF793E.xml @@ -0,0 +1,117 @@ + + + +The terrestrial microsnail genus Aulacospira Moellendorff, 1890 (Eupulmonata, Stylommatophora, Hypselostomatidae) in Thailand with key to Thai species + + + +Author + +Dumrongrojwattana, Pongrat +Department of Biology, Faculty of Science, Burapha University, Bangsaen, Chonburi 20131 Thailand +https://orcid.org/0000-0002-2544-6979 +oldsnails@hotmail.com + + + +Author + +Tanmuangpak, Kitti +Program of Biology, Department of Science, Faculty of Science and Technology, Loei Rajabhat University, Loei 42000 Thailand + +text + + +ZooKeys + + +2020 + +980 + + +23 +42 + + + + +http://dx.doi.org/10.3897/zookeys.980.54100 + +journal article +http://dx.doi.org/10.3897/zookeys.980.54100 +1313-2970-980-23 +78EED563089C4804A91087DAF1B3D2EB +FD77063CAE3F5DDFA5D3A7714A674E83 + + + + +Aulacospira smaesarnensis Panha & Burch, 2001 +Figures 2F +, 3D + + + + +Aulacospira smaesarnensis +Panha and Burch 2001 +: 65, fig. 2. + + + +Type locality. + +Thailand, Smaesarn Village, a fishery village located in an isolated liestone hill of Chonburi Province; +12°34'06"N +, 100°56'578"E. + + + +Types examined. + +ZRCBUU 0370 (10 shells); Thailand, Smaesarn Village, a fishery village located in an isolated liestone hill of Chonburi Province; +12°34'06"N +, 100°56'578"E; 12.v.2013; leg. Dumrongrojwattana, P. ZRCBUU 0425 (10 shells); Thailand, Smaesarn Village, a fishery village located in an isolated limestone hill of Chonburi Province; +12°34'06"N +, 100°56'578"E; 20.iii.2015; leg. Dumrongrojwattana, P. + + + +Measurements. +H = 2.47-2.83 mm, W = 1.45-1.70 mm. + + +Diagnosis. + +Shell minute, helicoid, moderately elevated spire; brownish. Protoconch smooth; teleoconch rough; body whorl large, rounded peripherally; tuba projecting downward; peristome thickened and expanded; aperture with poorly developed barriers, parietal lamella palatal plica and columellar lamella (Fig. +2F +). + + + +Radula. + +As in + +A. depressa + +(Fig. +3D +). + + + +Reproductive anatomy. +Unknown. + + +Distribution. + +This species appears limited to the type locality (Fig. +1 +). + + + + \ No newline at end of file diff --git a/data/38/27/3F/38273F69FFFB9714FF6C1F8EF139F9BF.xml b/data/38/27/3F/38273F69FFFB9714FF6C1F8EF139F9BF.xml new file mode 100644 index 00000000000..52ac7715088 --- /dev/null +++ b/data/38/27/3F/38273F69FFFB9714FF6C1F8EF139F9BF.xml @@ -0,0 +1,255 @@ + + + +A new species of Lycoderes Sakakibara (Hemiptera, Membracidae, Stegaspidinae) from Brazil + + + +Author + +Creão-Duarte, Antonio José + + + +Author + +Cabral, Valberta Alves + + + +Author + +Lourenço, Aline + +text + + +Zootaxa + + +2017 + +4281 + + +1 + + + +journal volume +28731 +10.11646/zootaxa.4281.1.5 +1f3f2b2b-5f1f-4d99-8e51-614be7703abd +1175-5326 +815778 +1ED07DCA-9BBD-488D-9FAB-479E934E9C9B + + + + + + + +Lycoderes albinoi +Creão-Duarte & Cabral + +sp. nov. + + + + +( +Figs. 1–4 +) + + + + +Diagnosis +. Body dark brown, almost black, except for forewings, with large central hyaline area, and abdomen, yellow; anterior pronotal process vertical, elevated, with suprahumeral horns arising at apex, divergent in frontal view, spatulate, longer than wide, tricarinate; posterior process sickle-shaped, extending from base of anterior process, arched and well separated from scutellum anteriorly, distal half tectiform, tapering to acute apex, extended slightly beyond apex of clavus. + +Measurements (in millimeters): Male/female. Total length (head to apex of forewings) 5.85/6.06; pronotum length (projection of suprahumeral horns to apex of posterior process) 5.37/5.49; length of forewings 5.36/5,48; width between humeral angles 1.71/1.91; width of head across eyes 1.67/1.77; head height 0.88/0.94; distance between eyes 1.12/1.23; distance between ocelli 0.46/0.50. + + + +FIGURES 1–4. + +Lycoderes albinoi + + +sp. nov +. + +1–2 male holotype in lateral and frontal view (MZSP). 3–4 female paratype in lateral and frontal view (DSEC). 5–6 +Lycoderides capixaba +Sakakibara, 2013, female in frontal and lateral view (DSEC); 7, +Lycoderides capixaba +Sakakibara, 2013, male in lateral view (DSEC). Scale bar = 1.0 mm. + + + + +Description +. + +Holotype +male + +. +Coloration +. Head, pronotum, ventral surface of thorax and legs dark brown, except for central area of forewings, hyaline, and eyes, ocelli and abdomen, yellow; head, legs and thorax with whitish and waxy pubescence; hind tibiae light brown, and tarsi yellow. +Head +( +Fig. 2 +). Approximately 1.5x wider than long, eyes hemispherical, ocelli small, above centro-ocular line; postclypeus trilobed in frontal view. +Thorax +. Pronotum ( +Fig. 1 +) densely punctate, punctations coarser on posterior process; short, decumbent setae throughout; median carina weaker in metopidium, percurrent and sharper along posterior process; suprahumeral horns Vshaped in anterior view, spatulate, longer than wide, tri-faceted, delimited by carinae on anterior and posterior margins and on ventral surface from apex to base of posterior process; in lateral view, metopidium slightly curved anteriorly, short, not exceeding suprahumeral horns in length; posterior process sickle-shaped, extending from base of anterior process, sharply curved and well separated from scutellum anteriorly, distal half tectiform, tapering towards acute apex, reaching beyond apex of clavus; forewings ( +Fig. 1 +) obliquely truncate at apex; one discoidal cell, five apical cells: fourth cell triangular, not petiolate, and fifth cell pentagonal; two crossveins: +r-m +fused to branch M1+2 and +m-cu +to branches M3+4. Legs with tibiae spatulate, metathoracic tibiae with cucullate setae in distal half of row II. + +Female (Figs. 3,4): similar to male, slightly larger and lighter in color; proximal half of posterior process less sharply curved. + + +Material +examined. + +Holotype +male + +, “ +Brasil +, BA[HIA], +Uma +| +Fazenda +UNACAU | + +7-24.X.1986 + +/D. S. Amo- | rim & +C. Vasconcelos +”; “ +Mata Atlântica Primária +| +Armadilha Luminosa +” ( +DSEC +/ +UFPB +). +Paratype +female with same label data as +holotype + +. + + + + + +Notes on +type +specimens + +. Specimens in good state of preservation. The +holotype +lacks the right suprahumeral horn. The left suprahumeral horn is missing in the female +paratype +, as well as the tarsi of both metathoracic legs. There is slight variation in the position of the crossvein +r-m +in the +type +series, however, in both the +holotype +and the +paratype +it is located at the base of M1+2 after the M fork. The crossvein +r-m +is a little farther from the fork in the holotype’s left forewing, and right after the point of bifurcation of M in the right forewing of the female, which is anomalous in this regard. In all cases, the fourth apical cell in the forewings is distinctly triangular. + + + + +Remarks. +In comparison to other congeneric species, + +Lycoderes albinoi + + +sp. nov. + +most closely resembles + +Lycoderes ancora +(Germar) + +and + +Lycoderes furcifer +Sakakibara. In + +females of + +Lycoderes ancora + +, the suprahumeral horns diverge next to the base of the posterior process, whereas in females of + +Lycoderes +. +albinoi + + +sp. nov. + +, the anterior process is more elongate, so that the suprahumeral horns diverge farther from the base of the posterior process. In males of + +Lycoderes ancora + +, the base of the posterior process is wider, reaching the base of the suprahumeral horns, a condition that is not observed in males of + +Lycoderes albinoi + + +sp. nov. + +due to the much narrower base of the posterior process. The base of the posterior process is also close to the base of the suprahumeral horns in males and females of + +Lycoderes furcifer + +, however, the tip of the posterior process does not reach the apex of the clavus, as it does in + +Lycoderes albinoi + + +sp. nov. + +In males of + +Lycoderes furcifer + +, the suprahumeral horns are tapered acutely towards the distal tips, and slightly curved ventrally. Contrastingly, the suprahumeral horns are gradually broadened toward the distal half in males of + +Lycoderes albinoi + + +sp. nov. + +, forming a dorsal angle in frontal view, then tapering from the distal third to an acute tip. + + + + +Etymology +. This species is dedicated to Dr. Albino Morimasa Sakakibara, for his lifelong work training new systematists focused on auchenorrhynchan +Hemiptera +, and for his outstanding contributions to treehopper taxonomy. + + + + \ No newline at end of file diff --git a/data/38/27/63/382763CE6AB8E2C64E80B61AE06B28A9.xml b/data/38/27/63/382763CE6AB8E2C64E80B61AE06B28A9.xml new file mode 100644 index 00000000000..b593d97ef61 --- /dev/null +++ b/data/38/27/63/382763CE6AB8E2C64E80B61AE06B28A9.xml @@ -0,0 +1,100 @@ + + + +Flora der Schweiz und angrenzender Gebiete. Band 3. Plumbaginaceae bis Compositae (2 nd edition): Rubiaceae + + + +Author + +Hess, Hans Ernst + + + +Author + +Landolt, Elias + + + +Author + +Hirzel, Rosmarie + +text + +1976 +Birkhaeuser Verlag + + +https://doi.org/10.5281/zenodo.292249 + +book +292249 +10.5281/zenodo.292249 +3-7643-0556-8 + + + +<subSubSection id="95F7AF5F70F2F225447BEBEFC2DF271C" pageId="null" pageNumber="281" type="nomenclature"> +<paragraph id="E0B7A2E4A169373C8E48686B79744536" pageId="null" pageNumber="281"> +<taxonomicName id="8EB24A5FB1E58A96AB6BC87A594EFC67" authority="L." class="Insecta" family="Muscidae" genus="Crucianella" kingdom="Animalia" order="Diptera" pageId="null" pageNumber="281" phylum="Arthropoda" rank="genus"> +<pageBreakToken id="E8A51C8AECC1C722EBB105440FA1C172" pageId="null" pageNumber="281" start="start"> +<normalizedToken id="E5D26ECA5159A95CB17F5A60B4C29DB1" originalValue="Crucianélla" pageId="null" pageNumber="281">Crucianella</normalizedToken> +</pageBreakToken> +<authorityName id="1F5FC55F238672FEA0FCE45F6EA3E752" pageId="null" pageNumber="281">L.</authorityName> +</taxonomicName> +</paragraph> +</subSubSection> +<subSubSection id="B4B25513EA0A3FB9C7B455EE1D18F54C" pageId="null" pageNumber="281" type="vernacular_names"> +<paragraph id="FBA42816C9F2FA6D1C4A6D48A37703A6" pageId="null" pageNumber="281">Kreuzblatt</paragraph> +</subSubSection> + + + +Unterscheidet sich von der Gattung + +Galium + +(S. 286) durch folgende Merkmale: + +Blueten +ungestielt + +, meist einzeln in der Achsel von +Tragblaettern +und mit +Vorblaettern +, + +zu 2- oder 4zeiligen, +beblaetterten +Aehren + +angeordnet. Krone mit mindestens 2 mm langer +Kronroehre +und 4-5 flach ausgebreiteten, + +an der Spitze +einwaertsgebogenen +Zipfeln; + +freier Teil der Krone bedeutend +kuerzer +als der verwachsene Teil. + + +Die Gattung + +Crucianella + +umfasst + +etwa 30 vorwiegend mediterrane und +suedwestasiatische +Arten. + + + + + \ No newline at end of file diff --git a/data/38/27/64/38276431338C5AB78D07B9994708ACBC.xml b/data/38/27/64/38276431338C5AB78D07B9994708ACBC.xml new file mode 100644 index 00000000000..2397999d67d --- /dev/null +++ b/data/38/27/64/38276431338C5AB78D07B9994708ACBC.xml @@ -0,0 +1,138 @@ + + + +Re-circumscription of the mimosoid genus Entada including new combinations for all species of the phylogenetically nested Elephantorrhiza (Leguminosae, Caesalpinioideae, mimosoid clade) + + + +Author + +O'Donnell, Shawn A. +https://orcid.org/0000-0003-0731-7425 +Department of Geography and Environmental Sciences, Northumbria University, Newcastle upon Tyne, NE 1 8 ST, UK +shawn.odonnell@cantab.net + + + +Author + +Ringelberg, Jens J. +https://orcid.org/0000-0003-0567-5210 +Department of Systematic and Evolutionary Botany, University of Zurich, 8008 Zurich, Switzerland + + + +Author + +Lewis, Gwilym P. +https://orcid.org/0000-0003-2599-4577 +Accelerated Taxonomy Department, Royal Botanic Gardens, Kew, Richmond, TW 9 3 AE, UK + +text + + +PhytoKeys + + +2022 + +2022-08-22 + + +205 + + +99 +145 + + + + +http://dx.doi.org/10.3897/phytokeys.205.76790 + +journal article +http://dx.doi.org/10.3897/phytokeys.205.76790 +1314-2003-205-99 +4024A478048757B197E5CF8734331A9E + + + + + +Entada obliqua (Burtt Davy) S.A. +O'Donnell +& G.P. Lewis + +comb. nov. + + + + += Elephantorrhiza obliqua Burtt Davy var. glabra +E. Phillips, Bothalia 1: 189. 1923. + + + + +Type +. + + + +SOUTH AFRICA +. Transvaal, between +Carolina +and Oshoek, ~ +1.6 km +from + +Robinson's +Farm, +J. Burtt Davy 2976 + +( +holotype +: BM [BM000081856]; isotypes: FHO, K [K000232281]) + +. + + + +Basionym. + + +Elephantorrhiza obliqua + +Burtt Davy, Bull. Misc. Inform. Kew 1921: 191. 1921. + + + +Description. + +Geoxylic suffrutex with erect, annual, usually unbranched stems up to 30 cm from underground axes, stems pubescent to glabrous. +Leaves +: primary and secondary axes glabrous to sparsely pubescent; petiole 2-6 cm long; rachis (0-)1.5-9 cm long; pinnae (1-)2-6 pairs per leaf, 2-11 cm long, with 4-13(-21) pairs of leaflets; leaflets 5.5-15 +x +2-6.5 mm, distinctly asymmetric, ovate to oblong-ovate, apex acute or mucronate, base oblique, mid-rib running from distal corner of leaflet base to apex centre, lamina glabrous. +Inflorescence +: an axillary spiciform raceme, 3.5-6 cm long, solitary, rachis glabrous to sparsely pubescent. +Flowers +: yellowish-white, pedicels 1.5 mm long, with minute red glands at base; calyx campanulate, 2 mm long, shallowly toothed, glabrous; petals 4.5 mm long; stamen filaments 7.5 mm long. +Fruit +: a laterally compressed, straight craspedium, 11 +x +4 cm, lacking transverse septa between seeds, thus leaving the valves to separate from the replum intact upon ripening, the epicarp exfoliating from the endocarp. +Seeds +: mature seeds not seen. + + + +Distribution. +South Africa, restricted to the Transvaal. + + +Habitat and ecology. +In grassland. + + + \ No newline at end of file diff --git a/data/38/27/B3/3827B376631954A7252C732A6D8E43A6.xml b/data/38/27/B3/3827B376631954A7252C732A6D8E43A6.xml new file mode 100644 index 00000000000..216c89289b0 --- /dev/null +++ b/data/38/27/B3/3827B376631954A7252C732A6D8E43A6.xml @@ -0,0 +1,169 @@ + + + +Two new species of Geejayessia (Hypocreales) from Asia as evidenced by morphology and multi-gene analyses + + + +Author + +Zeng, Zhao-Qing + + + +Author + +Zhuang, Wen-Ying + +text + + +MycoKeys + + +2018 + +42 + + +7 +19 + + + + +http://dx.doi.org/10.3897/mycokeys.42.27664 + +journal article +http://dx.doi.org/10.3897/mycokeys.42.27664 +1314-4049--7 + + + + +Geejayessia clavata Z.Q. Zeng & W.Y. Zhuang +sp. nov. +Figures 2, 3 + + + +Holotype. + +CHINA, Henan Province, Longyuwan, +33°40'45"N +, +111°46'26"E +, alt. 1500 m, on bark of +Buxus +sp., 17 September 2013, H.D. Zheng, Z.Q. Zeng & Z.X. Zhu 8728 (holotype: HMAS 275654), dried ex-type culture HMAS 248725. + + + +Etymology. +The specific epithet refers to the clavate microconidia. + + +Description. + +Mycelium not visible around ascomata or on host. Ascomata perithecial, crowded in group of 5 to 40, on basal stroma, oval, subglobose to globose, smooth, bright red when fresh, red brownish to dark red when dry, with a darker red ostiolar region, turning purple red in KOH and orange yellow in LA, 128-175 +x +206-255 +μm +(n = 17). Perithecial wall consisting of a single layer, 15-25 +μm +thick, cells forming textura prismatica, 2-12 +x +2-6 +μm +, walls 1-1.2 +μm +thick. Asci cylindrical, with a rounded apex, (4-7-)8-spored, 55-75 +x +5-9 +μm +. Ascospores ellipsoidal to broadly ellipsoidal, equally 2-celled, slightly constricted at septum, smooth or finely verruculose, hyaline or pale brown, obliquely uniseriate in ascus often with ends overlapping, 7.5-12 +x +4.5-5.5 +μm +. + + + +Culture characteristics. + +Colony on PDA 48 mm diam. after 7 d at 25 °C, surface cottony, aerial mycelium white, producing vinaceous pigment in medium. Colony on SNA 30 mm diam. after 7 d at 25 °C, surface slightly floccose, with sparse whitish aerial mycelium. Colony on CMD 56 mm diam. after 7 d at 25 °C, surface floccose, with sparse whitish aerial mycelium, producing vinaceous pigment in medium. Conidiophores with short simple branches. Conidiogenous cells monophialidic, cylindrical, tapering toward the tip, 12-63 +x +1.5-3.5 +μm +. Conidia clavate, not in chains, hyaline, aseptate, 4-7 +x +0.8-2 +μm +(n = 60). Macroconidia and chlamydospores not observed. + + +Notes. Attempts were made to obtain macroconidia of the fungus in culture, but failed. Although the falcate macroconidia are lacking, the major phenotypic features of the fungus, such as occurrence on bark of +Buxus +sp., perithecia broadly ampulliform with a short neck, asci cylindrical with a rounded apex, ellipsoidal ascospores uniseptate and conidiophores monophialidic, fit well with the generic concept of +Geejayessia +. The molecular data confirm the taxonomic placement and indicate its close relationship with +G. atrofusca +(Figure 1, BIPP/MPBP = 100%/89%). +Geejayessia atrofusca +differs significantly in dark brown to black ascomata that do not change colour in KOH or LA, wider asci [(7.5-)9.8-13.3(-15) +μm +wide] and longer ascospores [(10-)11.2-14.2(-17.0) +μm +long]. Its microconidia are oblong to slightly curved and falcate but not clavate and are longer and wider ( +Samuels and Rogerson 1984 +). + + + +Figure 2. +Geejayessia clavata +sexual state (holotype, HMAS 275654): +a-c +Ascomata on natural substrate +d-f +colour of perithecium in water (d), 3% KOH (e) and 100% lactic acid (f) g median section through perithecium +h-k +Asci with ascospores +l-o +Ascospores. Scale bars: 1 mm ( +a-c +); 100 +μm +( +d-f +); 50 +μm +(g); 10 +μm +( +h-k +), 5 +μm +( +l-o +). + + + + +Figure 3. +Geejayessia clavata +asexual state (HMAS 248725): +a-c +colony on PDA (a) SNA (b) and CMD (c) +d-j +conidiophores, phialides and/or microconidia on SNA. Scale bar: 10 +μm +( +d-j +). + + + + + \ No newline at end of file diff --git a/data/38/28/80/38288001D9C59685E4D1892F220E025B.xml b/data/38/28/80/38288001D9C59685E4D1892F220E025B.xml new file mode 100644 index 00000000000..5b7762d1ca7 --- /dev/null +++ b/data/38/28/80/38288001D9C59685E4D1892F220E025B.xml @@ -0,0 +1,63 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828-4-9042 + + + + + +Charitopes +Foerster +, 1869 + + + + + +ADIASTOLA +Foerster +, 1869 + + + +Notes + +Some distribution data from +Townes (1983) +and +Horstmann (1998a) +. + + + + \ No newline at end of file diff --git a/data/38/28/88/38288844EDF48AA557EDA975CA7621F8.xml b/data/38/28/88/38288844EDF48AA557EDA975CA7621F8.xml new file mode 100644 index 00000000000..acc5991d30a --- /dev/null +++ b/data/38/28/88/38288844EDF48AA557EDA975CA7621F8.xml @@ -0,0 +1,109 @@ + + + +Taxonomic revision of the rock-dwelling door snail genus Montenegrina Boettger, 1877 (Mollusca, Gastropoda, Clausiliidae) + + + +Author + +Feher, Zoltan + + + +Author + +Szekeres, Miklos + +text + + +ZooKeys + + +2016 + +599 + + +1 +137 + + + + +http://dx.doi.org/10.3897/zookeys.599.8168 + +journal article +http://dx.doi.org/10.3897/zookeys.599.8168 +1313-2970-599-1 +8BEE967F7C6946928210A440AD8E2018 +8BEE967F7C6946928210A440AD8E2018 + + + +Taxon classification Animalia Stylommatophora Clausiliidae + + + +Montenegrina prokletiana prokletiana +ssp. n. +Fig. 24F + + + +Diagnosis. +Very small, slender subspecies with strongly inflexed neck, weak basalis, but long subclaustralis. + + +Description. + +The light brown shell is very small and slender, its +81/2 +to +101/2 +whorls are separated by a deep suture. The lower three whorls are almost of the same width. Except the finely costate neck the entire shell surface is smooth. The strong inflection of the neck extends to the ventral side. The basal crest is weak, the peripheral one is strong. The light brown peristome is inflexed at the parietal side. The swollen and deflexed peristome margin is absent at the upper columellar side. The strong, projected lamella superior barely overlaps with the spiralis. The lamella inferior is weakly emerged, it turns horizontal before ending. In front view the medium-bent subcolumellaris is visible. Neither the inferior, nor the subcolumellaris reach the peristome margin. The dorsolateral lunella is not connected to the residual basalis. The subclaustralis is long and well developed, the sulcalis is present. The anterior plica superior is missing. The clausilium plate is not or only barely visible through the aperture. + + + +Dimensions +(in mm). Holotype Hs: 10.8, Ws: 2.7, Ha: 2.6, Wa: 2.1; paratypes (HNHM 99491, n = 12): Hs: 9.1-11.0 (mean 9.9, S.D. 0.66), Ws: 2.4-2.8 (mean 2.6, S.D. 0.12), Ha: 2.3-2.7, Wa: 1.9-2.2. + + +Differential diagnosis. + +The new subspecies differs from +Montenegrina prokletiana kovacsorum +ssp. n. by its smaller size, non-marginal lamellae inferior and subcolumellaris, as well as its well developed subclaustralis. + + + +Type locality. + +Albania, +Tropoje +District, Dragobi (14 km N of Bajram Curri), gorge of the +Perroi +i +Thate +, 540 m, +42.4364°N +, +19.9846°E +. + + + +Type material. +Type locality, leg. TD, ZE, ZF, DM, 6.x.2005, holotype (HNHM 99490), paratypes (HNHM 99491/3a+24, NHMW 111223/5a, MMM-B01326/25, ER/24, SZ/4); same locality, leg. ZB, Somogyi, 12.viii.2012, paratypes (HNHM 99492/13a+3aj). + + +Etymology. +The new taxon is named after the Prokletije Mts, the area where this species is distributed. + + +Distribution. +Northern Albania, Valbona Valley in the southern part of the Prokletije Mts. Known only from the type locality (Fig. 26). + + + \ No newline at end of file diff --git a/data/38/28/97/3828975026A3E2215C91520E6049AB67.xml b/data/38/28/97/3828975026A3E2215C91520E6049AB67.xml new file mode 100644 index 00000000000..79422ff812b --- /dev/null +++ b/data/38/28/97/3828975026A3E2215C91520E6049AB67.xml @@ -0,0 +1,87 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part G) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +529 +556 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Geranium peltatum +Linnaeus + +, + +Species Plantarum +2 + +: 678. 1753 + + +. + + + +"Habitat in Africa." RCN: 4944. + + + + +Lectotype +(Ghafoor in Jafri & El-Gadi, +Fl. Libya +63: 39. 1978): Herb. Linn. No. 858.12 ( +LINN +) + +. + + + + +Current name: + +Pelargonium peltatum +(L.) + +L'Her +. ( +Geraniaceae +). + + + + \ No newline at end of file diff --git a/data/38/28/C2/3828C27FCCE2FA72971AEE95B493CE95.xml b/data/38/28/C2/3828C27FCCE2FA72971AEE95B493CE95.xml new file mode 100644 index 00000000000..0b524fce7b4 --- /dev/null +++ b/data/38/28/C2/3828C27FCCE2FA72971AEE95B493CE95.xml @@ -0,0 +1,143 @@ + + + +Flora der Schweiz und angrenzender Gebiete. Band 3. Plumbaginaceae bis Compositae (2 nd edition): Labiatae + + + +Author + +Hess, Hans Ernst + + + +Author + +Landolt, Elias + + + +Author + +Hirzel, Rosmarie + +text + +1976 +Birkhaeuser Verlag + + +https://doi.org/10.5281/zenodo.292249 + +book +292249 +10.5281/zenodo.292249 +3-7643-0556-8 + + + +<subSubSection id="B2031852C2DB01ADB10416415AEAA70C" pageId="null" pageNumber="110" type="nomenclature"> +<paragraph id="939AE384A908BF57428F5FD25D712067" pageId="null" pageNumber="110"> +<taxonomicName id="22B70458A34F3B5919D13CC75EBC666A" authority="L." class="Magnoliopsida" family="Lamiaceae" genus="Marrubium" kingdom="Plantae" order="Lamiales" pageId="null" pageNumber="110" phylum="Tracheophyta" rank="species" species="vulgare"> +<pageBreakToken id="917DB6AE140147DD8E8077F0308B1993" pageId="null" pageNumber="110">Marrubium</pageBreakToken> +<normalizedToken id="3233EC4A830725AB8F16032C52B2FB9B" originalValue="vulgáre" pageId="null" pageNumber="110">vulgare</normalizedToken> +<authorityName id="5A512441040ED745E295D0DE73FFF06E" pageId="null" pageNumber="110">L.</authorityName> +</taxonomicName> +</paragraph> +</subSubSection> +<subSubSection id="B3EC7CB9DE9B95394739A7AA0ED93E1D" pageId="null" pageNumber="110" type="vernacular_names"> +<paragraph id="1676D66ED3FA292EEBAD602E032F7648" pageId="null" pageNumber="110"> +<normalizedToken id="72F6740224477144278372C7E89273DA" originalValue="Gewöhnlicher" pageId="null" pageNumber="110">Gewoehnlicher</normalizedToken> +Andorn +</paragraph> +</subSubSection> + + + +Ausdauernd, mit Pfahlwurzel; nur schwach riechend; 30-60 cm hoch. Stengel aufrecht oder aufsteigend, +dicht filzig behaart +(Haare einfach, mehrzellig und oft +sternfoermig +verzweigt). +Blaetter +gestielt, breit oval, 2-4 cm lang und fast so breit, stumpf und +unregelmaessig +gezaehnt +, besonders unterseits + +dicht und +weissfilzig +behaart. + +Blueten +kurz gestielt, in dichten (fast kugeligen), +vielbluetigen +, +quirlaehnlichen +Bluetenstaenden +in den Achseln der +Blaetter +. Kelch 4-6 mm lang, dicht mit Sternhaaren bedeckt, mit +10 stacheligen +( +zur Fruchtzeit hakigen +) + +Zaehnen +. + +Krone 6-7 mm lang, + +weiss +. + +Teilfruechte +etwa 2 mm lang, mit dem Kelch abfallend. + + +Zytologische Angaben. 2n += +34: +Material aus +Grossbritannien +(Rutland 1941), aus Nordamerika (Epling in Heiser und Whitaker 1948), von den Kanaren (Larsen 1960), aus Peru (Diers 1961), aus der +Aegaeis +(Bothmer 1970,) aus Bulgarien (Markova und Ivanova in +Loeve +1971b). +2n += +36: +Material aus Norddeutschland (Wulff 1939c). + + +Standort. +Kollin und montan. Trockene, stickstoffreiche +Boeden +in warmen Lagen. +Wegraender +, +Viehlaegerstellen +, +Schuttplaetze +. +Onopordetum acanthii +Br.-Bl. 1922. + + +Verbreitung. Mediterrane Pflanze: +Ganzes Mittelmeergebiet ( +ostwaerts +bis Zentralasien); +frueher +als Heilpflanze kultiviert und im +uebrigen +Europa und in Amerika weit verbreitet. - Im Gebiet vor allem +Elsass +, Savoyen, +Dep +. Ain, Wallis, Aostatal, Ossola, Veltlin, Bergamasker Alpen, Vintschgau, Oberinntal, Domleschg; sonst selten. + + + + \ No newline at end of file diff --git a/data/38/28/CA/3828CA1F9BBFC015B277BD26E712A0F0.xml b/data/38/28/CA/3828CA1F9BBFC015B277BD26E712A0F0.xml new file mode 100644 index 00000000000..2b64c021a27 --- /dev/null +++ b/data/38/28/CA/3828CA1F9BBFC015B277BD26E712A0F0.xml @@ -0,0 +1,99 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part C) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +370 +473 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Celtis orientalis +Linnaeus + +, + +Species Plantarum +2 + +: 1044. 1753 + + +. + + + +"Habitat in Indiis." RCN: 7646. + + + +Lectotype +(Soepadmo & Edi Hamli in Soepadmo, +Tree Fl. Sabah Sarawak +2: 399. 1996): Herb. Hermann 2: 2; 4: 71, No. 369 (BM). + + + + +Current name: + + +Trema orientalis + +(L.) Blume + +( +Ulmaceae +). + + + + +Note: +Polhill (in +Kew Bull. +19: 143. 1964), and some later authors, have indicated material in Herb. Hermann 2: 2; 4: 71 (BM) as syntypes but as the use of this term implies no intention to indicate a single nomenclatural type (unlike the use of +holotype +, +lectotype +or +neotype +), this is not regarded as a correctable error. Soepadmo & Edi Hamli, however, indicated the same material simply as +"type" +. Although there is material in two volumes, it appears to have been part of a single gathering, so their statement is accepted as the first typification (Art. 9.15). + + + + \ No newline at end of file diff --git a/data/38/28/E8/3828E873A56E5E719F3188E14080E682.xml b/data/38/28/E8/3828E873A56E5E719F3188E14080E682.xml new file mode 100644 index 00000000000..48f918ee51e --- /dev/null +++ b/data/38/28/E8/3828E873A56E5E719F3188E14080E682.xml @@ -0,0 +1,151 @@ + + + +Psychodidae (Diptera) of Azerbaijan and Georgia - faunistics with biodiversity notes + + + +Author + +Jezek, Jan +Department of Entomology, National Museum, Cirkusova 1740, CZ - 193 00 Praha 9 - Horni Pocernice, Czech Republic + + + +Author + +Manko, Peter +https://orcid.org/0000-0003-1862-9117 +Department of Ecology, Faculty of Humanities and Natural Sciences, University of Presov, 17. novembra 1, SK - 081 16 Presov, Slovakia +peter.manko@unipo.sk + + + +Author + +Obona, Jozef +https://orcid.org/0000-0002-1185-658X +Department of Ecology, Faculty of Humanities and Natural Sciences, University of Presov, 17. novembra 1, SK - 081 16 Presov, Slovakia + +text + + +ZooKeys + + +2021 + +2021-06-15 + + +1049 + + +15 +42 + + + + +http://dx.doi.org/10.3897/zookeys.1049.66063 + +journal article +http://dx.doi.org/10.3897/zookeys.1049.66063 +1313-2970-1049-15 +E0AEB4DB6C32407697542AA74386C517 +F43B77514DD55AC69BA1E334AE61ABF2 + + + + +Psychodocha gemina (Eaton, 1904) + + + +Material examined. + + + +Azerbaijan + +: A 05, +1.10.2019 +, +1♀ +, slide Inv. No. 25579, leg. PM; A 23 + +, +6.5.2019 +, +1♀ +, slide Inv. No. 25685, leg. JO. + + +Georgia + +: G 09, +2.5.2019 +, +1♀ +, slide Inv. No. 25733, leg. JO; G 19 + +, +30.4.2019 +, +1♀ +, slide Inv. No. 25651, leg. JO; G 24, +29.4.2019 +, +1♂ +, +1♀ +, slide Inv. No. 25735 and 25748, leg. JO. + + + +Distribution. + +A common European species, it occurs commonly from lowlands to mountains. The larvae are saprobiotic and often develop in nests of water birds. Recorded from Austria, Belgium, Bosnia and Herzegovina, Croatia, Czech Republic, Great Britain, Denmark, France, Finland, Germany, Greece, Hungary, Ireland, Norway, Romania, Serbia, Slovakia, Slovenia, Spain, Switzerland, the Netherlands, Ukraine, and Georgia: Abkhazia ( + +Jezek +and Goutner 1995 + +; +Krek 1999 +; + +Jezek +2002 + +; +Kvifte et al. 2011 +, +2013 +; + +Jezek +and +Omelkova +2012 + +; +Salmela et al. 2014 +; + +Jezek +et al. 2017 + +; + +Obona +et al. 2019a + +). + + + +Note. +First record for Azerbaijan. + + + \ No newline at end of file diff --git a/data/38/29/A2/3829A2EDA1FBFE150FCA8699F75A055D.xml b/data/38/29/A2/3829A2EDA1FBFE150FCA8699F75A055D.xml new file mode 100644 index 00000000000..7c7a9982540 --- /dev/null +++ b/data/38/29/A2/3829A2EDA1FBFE150FCA8699F75A055D.xml @@ -0,0 +1,179 @@ + + + +An illustrated key to the cuckoo wasps (Hymenoptera, Chrysididae) of the Nordic and Baltic countries, with description of a new species + + + +Author + +Paukkunen, Juho + + + +Author + +Berg, Alexander + + + +Author + +Soon, Villu + + + +Author + +Odegaard, Frode + + + +Author + +Rosa, Paolo + +text + + +ZooKeys + + +2015 + +548 + + +1 +116 + + + + +http://dx.doi.org/10.3897/zookeys.548.6164 + +journal article +http://dx.doi.org/10.3897/zookeys.548.6164 +1313-2970-548-1 +D5D7B51E5AC6460D9B3C7584E46F9B3F +D5D7B51E5AC6460D9B3C7584E46F9B3F + + + + +Taxon +classification Animalia Hymenoptera Chrysididae + + + + + +Elampus constrictus ( +Foerster +, 1853) + +Figs 42, 45 + + + + +Notozus constrictus +Foerster +, 1853: 336. + + +Elampus productus +of authors, not Dahlbom, 1854. + + +Ellampus spina +of authors, not (Lepeletier, 1806). + + +Notozus panzeri +of authors, not (Fabricius, 1804). + + +Elampus constrictus +: +Morgan 1984 +: 7. + + + +Diagnosis. + +Length 4-7 mm. The species differs from +Elampus panzeri +and +Elampus foveatus +by the structure of the apical truncation of T3, which has pointed margins ventrally and resem +bles +a sickle or a boomerang in shape (Fig. 45). Sometimes the apical truncation is very narrow, similar to that of +Philoctetes truncatus +. The lateral margins of T3 are shallowly concave anterior to the apical truncation. As opposed to +Elampus panzeri +and +Elampus foveatus +, the scrobal carina reaches the angle of the omaulus (Fig. 42). Both sexes are usually bicoloured with a blue or greenish head and mesosoma, and a reddish metasoma. Entirely greenish or blue specimens are found occasionally. + + + +Distribution. + +Denmark, Estonia, Finland, Norway, Sweden. Relatively rare. - Trans-Palearctic: widely distributed in the Palearctic Region, from Europe to China ( +Rosa et al. 2014 +). + + + +Biology. + +Habitat: sparsely vegetated sandy areas, heaths. Adults occasionally visit flowers of +Apiaceae +and +Rosaceae +( +Linsenmaier 1997 +, +Rosa 2004 +). Flight period: May to July. Host: +Mimesa bicolor +(Jurine), +Mimesa equestris +(Fabricius) and +Mimesa lutaria +(Fabricius) ( +Crabronidae +) ( +Benno 1950 +, +Lomholdt 1975 +). + + + +Figures 38-46. Metascutellum, propodeum and T1, lateral view (arrow indicating metascutellar projection): 38 +Elampus foveatus +♀. T3, lateral view: 39 +Elampus panzeri +♀ 40 +Elampus foveatus +♀. Head, lateral view (arrow indicating genal setae): 41 +Elampus panzeri +♀. Mesopleuron, lateral view (arrow indicating junction of omaulus and scrobal carina): 42 +Elampus constrictus +♀ 43 +Elampus foveatus +♀. T3, postero-dorsal view: 44 +Elampus panzeri +45 +Elampus constrictus +♀ 46 +Elampus foveatus +♀. Scale 0.5 mm. + + + + + \ No newline at end of file diff --git a/data/38/2A/2F/382A2FE23DDE037FD450F22396381123.xml b/data/38/2A/2F/382A2FE23DDE037FD450F22396381123.xml new file mode 100644 index 00000000000..368faa89422 --- /dev/null +++ b/data/38/2A/2F/382A2FE23DDE037FD450F22396381123.xml @@ -0,0 +1,135 @@ + + + +Order Carnivora + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +532 +628 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Viverra megaspila +Blyth 1862 + + + + + + + +Viverra megaspila +Blyth 1862 + +, +J. Asiat. Soc. Bengal, 31: 331 + +. + + + + +Type Locality: + +"vicinity of Prome" [ +Burma +, Prome (= Pye) +18°49'N +, +95°13'E +]. + + + + + +Vernacular Names: +Large-spotted Civet +. + + + + +Distribution: +Burma +, +Cambodia +, +Laos +, +Malaysia +(West), +Thailand +, +Vietnam +. + + + + +Conservation: +IUCN +– Lower Risk (lc). + + + + +Discussion: +Does not include + +V. civettina + +; reviewed by +Lindsay (1928) +, + +Pocock (1941 +a +) + +, and + +Wozencraft (1989 +b +) + +. +Corbet and Hill (1992) +raised doubts as to their separation. + + + + \ No newline at end of file diff --git a/data/38/2A/49/382A493A1323B3744508717844E06EAE.xml b/data/38/2A/49/382A493A1323B3744508717844E06EAE.xml new file mode 100644 index 00000000000..f8cfbc57616 --- /dev/null +++ b/data/38/2A/49/382A493A1323B3744508717844E06EAE.xml @@ -0,0 +1,60 @@ + + + +The ground beetles (Coleoptera: Carabidae) of the Strandzha Mountain and adjacent coastal territories (Bulgaria and Turkey) + + + +Author + +Kostova, Rumyana + + + +Author + +Gueorguiev, Borislav + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8135 +8135 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8135 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8135 +1314-2828--8135 + + + + +Harpalus (Harpalus) punctatostriatus Dejean, 1829 + + + +Materials + + +Type status: +Other material +. Location: countryCode: BG; locality: +Ropotamo +; Record Level: bibliographicCitation: Hieke & Wrase (1988: 128) + + + + + \ No newline at end of file diff --git a/data/38/2A/87/382A8791AB404C6C6FAF15977D21FD8C.xml b/data/38/2A/87/382A8791AB404C6C6FAF15977D21FD8C.xml new file mode 100644 index 00000000000..e045d2cedb8 --- /dev/null +++ b/data/38/2A/87/382A8791AB404C6C6FAF15977D21FD8C.xml @@ -0,0 +1,347 @@ + + + +First record of Dissomphalus Ashmead (Hymenoptera: Bethylidae) from Russia with description of a new species + + + +Author + +Fadeev, Kirill I. + +text + + +Zootaxa + + +2022 + +2022-02-14 + + +5099 + + +3 + + +382 +390 + + + +journal article +20657 +10.11646/zootaxa.5099.3.6 +be91abb3-6da9-4daa-a4c7-0738597f1cf4 +1175-5326 +6079202 +65B88289-AF35-4C4F-B134-6E7CC35AC2BA + + + + + + + +Dissomphalus oksanae + +sp. nov. + + + + + + +( +Figs 1–3 +) + + +Description +. +Holotype +. Male. +Measurements. +Body length ca. 3.0 mm; forewing length +2.2 mm +, maximum forewing width +0.86 mm +, hind wing length +1.7 mm +, hind wing width +0.42 mm +; HL +0.5 mm +; HW +0.5 mm +; WF +0.33 mm +; OOL +0.2 mm +; EL +0.2 mm +; AOL +0.066 mm +; WOT +0.15 mm +; DAO +0.033 mm +; POL +0.066 mm +; LM +0.916 mm +; LP +0.2 mm +; WP +0.45 mm +; LMPD +0.33 mm +; WMPD +0.33 mm +. Width of hypopygium +0.33 mm +. + + +Colour. +Head and mesosoma dark brown. Tegula, pronotal collar, mandible, and antenna brown. Palpi beige. Metasoma from brown ventral part of petiole, to brown-orange. Legs from brown at base to pale yellow-brown. Wings hyaline, veins pale. Genitalia yellow, distal part of harpe light brown. + + +Head. +( +Fig. 1 B–G +) Head as long as wide. Mandible with three apical teeth; ventral tooth acute and largest ( +Fig. 1 G +). Median clypeal lobe weakly protruded anterad and ventrad and wedge-shaped with sides incurved and slightly undulating; apex rounded. Median clypeal carina low, incurved in lateral view. Lateral clypeal lobe moderately developed, rounded. Eye with short erect setae. Ocelli equal-sized and arranged in almost equilateral triangle, frontal angle of ocellar triangle acute. Occipital carina completed, thin, cellular at base, in height to 0.3 DAO. Head surface with reticulate pattern and slender sparse punctures spaced at least one seta’s length apart. First five antennomeres in ratio of 13:5:5:5: +5 in +length. Flagellomeres with sparse oval-pitted sensillae and erect setae. WF 0.66 × HW, WF 1.65 × EL, OOL 1.33 × WOT, POL = AOL, DAO 0.22 × WOT. + + + +Mesosoma +. + +( +Fig. 2 A–C +) Pronotum and mesonotum matte, with fine punctures and reticulate pattern dorsally and laterally. Dorsal pronotal area trapezoidal, with incurved posterior border. Transverse pronotal carina weakly expressed. LP 0.44 × WP. Anteromesoscutum elliptical, convex. Notauli distinct, narrow, not almost reaching posterior margin of mesoscutum, converging posteriorly. Parapsidal signum narrowly presented posteriorly. Posterior margin of mesoscutum with slender sulcus. Mesoscutellar disc triangular, with pair mesoscuto-scutellar pits anteriorly, forming together trapezoid depression extending posteriorly with posterior margin slightly incurved. Gap between these pits weakly expressed. Metanotal trough with longitudinal ridges. Mesopleuron reticulate, mesopleural pit and mesepimeral sulcus present. Metapectal-propodeal disc as long as wide, its posterior part rounded, posterior margin outcurved; metapostnotal median carina not reaching posterior margin of disc, present on 0.85 of anterior disc length, low and slightly sinuous, with short transverse wrinkles; lateral carina of metapectal-propodeal complex low; pair of transverse posterior carinae developed in anterior third of disc; basal triangular area of disc weakly reticulate-wrinkled; posterior third and lateral area of disc polish and shiny. + + +Wings. +( +Fig. 2 D +) Forewing with costal (C) and subcostal (Sc+R) veins closely placed and parallel, but rolledup anterior wing edge in photo. Pterostigma slender. Poststigmal abscissa of R1 vein thin, equal to half of 2r-rs&Rs vein. R1 vein as long as pterostigma. 2r-rs&Rs vein long and smooth. + + +Metasoma. +( +Fig. 1 H +, +2 E +) Рetiolate, smooth and shining. Metasomal tergum II with pair smooth oval depressions in its mediolateral part; depressions relatively large, distant each other about their maximum diameter, with one–three setae anterolaterally; small low tubercles in its median part without tuft of setae. Hypopygium ( +Fig. 3 G +) subtrapezoid, minimum width 0.56 × its maximum width, with anterior and posterior margins weakly incurved; anterior margin with long median spiculum as long as hypopygium and two pairs of anteromedial apodeme along sides; posterior margin with low median callus and two small lateral depressions. Median part of hypopygial plate in sparse long setae, their length up to half length of hypopygium. + + +Genitalia. +( +Fig. 3 A–F, H +) Very broad, mittens-like. Genital ring thin. Aedeagal dorsal valva at basal quarter with flat plate, emblem-shaped; median quarters with median ridge on dorsal surface turning into median rounded tooth; apical quarter with pair of apical lobes, membranous and leaf-like and rounded with row of fine setae on outer margin ( +Fig. 3 C +). Aedeagal ventral valve bifurcated; its parts wedge-shaped, elongated and narrowed distally, apex sharpened, as long as dorsal valve. Apical end of harpe sclerotized, hook-shaped, curved mesad, apex rounded with 5–6 apical setae. Volsella G-like shape ( +Fig. 3 F, H +), with seta on inner margin; basivolsella without tooth. Cuspis arched. Digitus with basal projection in form of curved back tooth. Apodeme reaching genital ring. + + + + +FIGURE 1. + +Dissomphalus oksanae + +sp. nov. +( + +♂; A–E, H—holotype; F, G—paratype). A. Habitus, lateral view. B. Clypeus, frontal view. C. Head, lateral view. D. Head, dorsal view. E. Antenna. F. Head, ventral view. G. Mandibles. H. Metasomal tergum I–II, dorsal view. Scale bars: 0.5 mm for A, E; 0.25 mm for B–C, F, H; 0.1 mm for G. + + + +Female. +Unknown. + + + + +Type material. + + +Holotype + +: + +, + +RUSSIA +, + + +Krasnodar +Territory + +, +Krasnodar +, VNIIBZR [= +All-Russian Research Institute of Biological Plant Protection +, +Entomological Reservation +], +45°02’56.1”N +38°52’32.4”E +, + +13.VII.2013 + +, +Malaise trap +, +O. Kosheleva +leg. ( +ZISP +) + +. + + +Paratypes + +: +8 ♂ +, with same labels as in +holotype +( +6 ♂ +in +ZISP +, +2 ♂ +in +ZMMU +). + + + + + +Biology. +Unknown. + + + + + +FIGURE 2. + +Dissomphalus oksanae + +sp. nov. + +(♂; A, B, D, E—holotype; C– paratype). A. +Mesosoma +, dorsal view. B. Mesosoma, lateral view. C. +Mesosoma +, ventral view. D. Forewing. E. Metasoma, dorsal view. Scale bars: 0.25 mm for A–C, E; 0.5 mm for D. + + + + + +FIGURE 3. + +Dissomphalus oksanae + +sp. nov. + +(♂; A, B, D, E, G—holotype; C, F, H—paratype). A. Genitalia, ventral view, from slide. B. Genitalia, dorsal view, from slide. C. Apical lobe of aedeagus, lateral view. D. Genitalia, ventral view. E. Genitalia, dorsal view. F. Volsella, dorsal view. G. Hypopygium, outer view. H. Volsella, ventral view. Scale bars: 0.25 mm for A, B, G; 0.1 mm for H. + + + + +Variation: +Forewing +length 2.0– +2.2 mm +, maximum forewing width +0.78–0.86 mm +; HL +0.50–0.53 mm +; HW +0.48–0.50 mm +; WF +0.30–0.33 mm +: LM +0.91–0.96 mm +; WP +0.42–0.45 mm +; LMPD +0.30–0.35 mm +; WMPD +0.27– 0.33 mm +. + + + +Distribution + +: +Russia +, +Krasnodar +Territory. + + +Etymology +. This species is named in honor to +Oksana +V. +Kosheleva +( +St Petersburg +, +Russia +), a +Russian +chalcidologist and expert for the family +Eulophidae +, who collected the +type +series of this species. + + + + +Remarks. +A new species is similar in external morphology to male of + +D. kyushuensis + +by having an elongated and single-toothed median lobe of clypeus, but differs of them by the following characters: 1) presence the sharp angle and a rounded apex of median lobe of clypeus ( +vs +median lobe dully angulate medially), 2) head, pronotum, and mesonotum finely punctured ( +vs +impunctate), 3) ocelli in an equilateral triangle ( +vs +in obtuse ocellar triangle), 4) mesoscuto-scutellar pits forming together trapezoid depression extending posteriorly with posterior margin slightly incurved, medial partition weakly expressed ( +vs +elongated rectangular depression non-separable into two pits), 5) metapectal-propodeal disc with the same width and length and its slightly outcurved sides, as well as rounded posterior side and posterior margin outcurved ( +vs +0.77 × as long as wide and parallel sides and posterior margin straight), 6) metapostnotal median carina metapectal-propodeal disc not reaching posterior margin of disc, present on 0.85 of disc length ( +vs +reaching posterior margin of disc), 7) metasomal tergum II with pair large and smooth depressions, with a pit on median part ( +vs +oval depressions laterally, depressions with a pit on its anterior portion). + +I do have not the morphological basis for comparing a male of a new species with the females of three known European species due to their great sexual dimorphism. + + + \ No newline at end of file diff --git a/data/38/2A/87/382A8791AB434C6B6FAF101F7F85F8C4.xml b/data/38/2A/87/382A8791AB434C6B6FAF101F7F85F8C4.xml new file mode 100644 index 00000000000..042c87eb61a --- /dev/null +++ b/data/38/2A/87/382A8791AB434C6B6FAF101F7F85F8C4.xml @@ -0,0 +1,175 @@ + + + +First record of Dissomphalus Ashmead (Hymenoptera: Bethylidae) from Russia with description of a new species + + + +Author + +Fadeev, Kirill I. + +text + + +Zootaxa + + +2022 + +2022-02-14 + + +5099 + + +3 + + +382 +390 + + + +journal article +20657 +10.11646/zootaxa.5099.3.6 +be91abb3-6da9-4daa-a4c7-0738597f1cf4 +1175-5326 +6079202 +65B88289-AF35-4C4F-B134-6E7CC35AC2BA + + + + + + +Genus + +Dissomphalus +Ashmead, 1893 + + + + + + + +Type-species +: + +Dissomphalus xanthopus +Ashmead, 1893 + +. + + + + +Synonyms. + +Ecitopria +Wasmann, 1899: 55 + +. +Type +species: + +Ecitopria crassicornis +Wasmann, 1899 + +. Synonymized by +Evans 1955 +. + + + + + +Psilobethylus +Kieffer, 1906: 461–462 + + +. +Type +species: + +Psilobethylus luteus + +Kieffer, +1906 + + +in Kieffer & Marshall 1904–1906. Synonymized by +Terayama 1995 +. + + + +For the complete list see + +Azevedo +et al. +(2018b) + + + + + +Diagnosis. +Body robust. Clypeus with median lobe usually unidentate or tridentate. Metasomal tergum II longer than I. Metasomal tergum II with pair of process, tubercles or pits, in most cases. Metasomal tergum III without modification. Hypopygium usually with three stalks, median stalk longer than lateral. Genitalia short and wide. Harpe curved inward. Aedeagus complex with dorsal valve and paired ventral valve. Volsella G-like shape. For the complete diagnosis of the genus see + +Azevedo +et al. +(2018b) + +. + + + + +Biology. +Nothing is known about the lifestyle and biology of the vast majority of species. In accordance with +Evans (1955 +, +1978 +), females of various species were taken in soil, logs, leaf litter, ant nests, packrat nests, males were taken in traps or by sweeping, and North American species + +D. apertus +Kieffer, 1914 + +was associated with + +Bruchus brachialis +Fahraeus + +( +Coleoptera +: +Bruchidae +), and + +D. xanthopus +Ashmead, 1893 + +was associated with +Micromalthidae (Coleoptera) +and +Cecidomyiidae (Diptera) +. + + + + +Distribution. +Worldwide (Australasian, Nearctic, Neotropical, Afrotropical, Oriental and Palaearctic regions) ( + +Azevedo +et al. +2018b + +). + + + + \ No newline at end of file diff --git a/data/38/2A/87/382A87CBFF87FFB1FF41B820FC04FD8D.xml b/data/38/2A/87/382A87CBFF87FFB1FF41B820FC04FD8D.xml new file mode 100644 index 00000000000..1b234dcaa24 --- /dev/null +++ b/data/38/2A/87/382A87CBFF87FFB1FF41B820FC04FD8D.xml @@ -0,0 +1,250 @@ + + + +A new species of the genus Mongolotettix Rehn, 1928 from Shandong, China (Acrididae, Acridoidea, Orthoptera) + + + +Author + +Shen, Wei-Xing +0000-0002-4664-320X +Taishan Forest Pest Control and Quarantine Station, Taian, Shandong 271000, China & swxemail @ 163. com; https: // orcid. org / 0000 - 0002 - 4664 - 320 X + + + +Author + +Jia, Chun-Yan +0000-0001-6883-3787 +Taishan Forest Pest Control and Quarantine Station, Taian, Shandong 271000, China & jcy 1231 @ 163. com; https: // orcid. org / 0000 - 0001 - 6883 - 3787 + + + +Author + +Yin, Zhan +College of Life Sciences, Hebei University, Baoding, Hebei, 071002, China + +text + + +Zootaxa + + +2022 + +2022-04-07 + + +5125 + + +1 + + +97 +100 + + + +journal article +54974 +10.11646/zootaxa.5125.1.7 +f58641d7-985e-4d84-8ec7-c3f5a35df63b +1175-5326 +6420512 + + + + + + + +Mongolotettix shandongensis + +sp. nov. + + + + + + +( +Figs. 1–12 +) + + + +Holotype + +, + + +paratype + +, +Shandong +, +Wendeng +, +Kunyushan +, 37º20´N, 121º80´E + +2009-8-13 + +, collected by +Yin Zhan +, +Mo +Tie-Lu & +Xu +Yong-Yu. + + + +Male +Body small in size. Head shorter than pronotum. Face oblique in profile. Frontal ridge slightly widened downward. Antennae ensiform, 20 segmented, extending distinctly over hind margin of pronotum. Eyes oval, vertical diameter 1.7 times horizontal diameter and 1.4 times length of subocular furrow. Pronotum median keel visible, distinctly cut by hind transverse sulcus, lateral keels almost parallel, prozona 1.3 times of metazona in length. Tegmina reaching the 2/3 of hind femur, apically concave in the middle, maximum width of cubital area 1.8 times minimum width of medial area, Cub vein reaching to the apex of tegmen. Interspace of mesosternum distinctly narrowed in the middle, length 4.2 times minimum width. Lateral lobes of metasternum separated. Upper keel of hind femur smooth, length of hind femur 5.3 times its maximum width, end of lower knee lobes angular, inner side with 108 stridulatory pegs. Hind tibia with 13 spines on inner and outer sides, external apical spine absent. Second metatarsomere shorter than the first. Tympanum large and round. Cercus long conical, almost reaching tip of epiproct. Furculae large, circular at apex. Subgenital plate long conical, length 1.9 times maximum width. Width of epiphallus larger than high. + +Female: Body more robust than male. Vertical diameter of eyes 1.6 times horizontal diameter and 1.2 times the length of subocular furrow. Prozona 1.5 times metazoan in length. Tegmina short, extending over the middle of 2nd abdominal tergite, length 2.8 times its maximum width. Interspace of mesosternum slightly narrowed in the middle, length 2.3 times minimum width. Length of hind femur 5.1 times its maximum width. Cercus short-conical, not reaching end of epiproct. Subgenital plate long, length 1.8 times width, hind margin angulated in the middle. Upper ovipositor valve longer, length 3.5 times maximum width, with small teeth on outer margin. +Coloration: Body brown. Antennae yellowish brown. Pronotum yellowish-brown. Tegmina of male with a white stripe on the fore margin at base. Tegmina of female with a black longitudinal stripe in the middle. Abdomen yellowishbrown, with a broad dark longitudinal stripe on both sides. Subgenital plate brown. + +Measurement (in mm): +Length of body: + +19.7, + +29.3 Length of tegmina: + +10.0, + +4.1 Length of hind femur: + +11.5, + +15.8. + + + + +Diagnosis. +The new species is similar to + +M. hubeiensis + +Zheng +et al +, 2017 + + +. The major differences are listed in +Table 1 +. + + + + + +FIGURES 1–12. + +Mongolotettix shandongensis + +sp. nov. + +1. body in lateral view ♂; 2. epiphallus, ♂; +3 +. head and pronotum in dorsal view ♂; 4. +h +ead Frontal view; 5. stridulatory pegs, ♂; 6. end of abdomen ♂; 7. mesosternum ♂; 8. tegmen ♂; 9. body in lateral view ♀; 10. end of abdomen in lateral view ♀; 11. mesosternum ♀; 12. end of abdomen ventral view ♀. 13–16 + + +Mongolotettix hubeiensis +Zheng + +, et +al +, 2017 + +13. tegmen ♂; 14. Epiphallus; 15. Tegmen; 16. end of abdomen in lateral view ♀ (figs. 13–15 after Zheng, +et al +, 2017). + + + + +TABLE 1. +Comparison of + +Mongolotettix shandongensis + + +sp. nov. + +and + +M. hubeiensis + +Zheng +et al +, 2017 + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Characters + +M. shandongensis + + +sp. nov. + + + +M. hubeiensis + +Zheng +et al +, 2017 + + +
Tegmina of maleWith white stripe on the fore margin at base, Cub vein reaching to the apex of tegmenWithout white stripe on the fore margin at base, Cub vein not reaching to the apex of tegmen
EpiphallusBoth posterior projections not narrow at apexBoth posterior projections narrow at apex
Tegmina of femaleLonger, extending over the middle of 2nd abdominal tergumShorter, extending over the hind margin of first abdominal tergum slightly
Upper ovipositor valveSlender, length 3.5 times its maximum widthShorter, length 2.8 times its maximum width
+
+ + +Etymology +The specific epithet is named for the +type +locality +Shandong +. + + +
+
\ No newline at end of file diff --git a/data/38/2A/87/382A87F70D11FFE888CB1A932B8228B2.xml b/data/38/2A/87/382A87F70D11FFE888CB1A932B8228B2.xml new file mode 100644 index 00000000000..23851cffc63 --- /dev/null +++ b/data/38/2A/87/382A87F70D11FFE888CB1A932B8228B2.xml @@ -0,0 +1,459 @@ + + + +Taxonomic revision of the Odontophrynus cultripes species group, with description of a new related species (Anura, Cycloramphidae) + + + +Author + +Caramaschi, Ulisses + + + +Author + +Napoli, Marcelo Felgueiras + +text + + +Zootaxa + + +2012 + +3155 + + +1 +20 + + + +journal article +45697 +10.5281/zenodo.212451 +ff28ec88-03cf-48a0-9798-d83735ab3d29 +1175-5326 +212451 + + + + + + + +Odontophrynus carvalhoi +Savage and Cei, 1965 + + + + + +Figures 4–6 + + + + + +Odontophrynus americanus + +—Miranda– +Ribeiro, 1937 +. + +Odontophrynus carvalhoi +Savage & Cei, 1965 + +. + + + + + +Holotype +. + +MNRJ +0 313 (fig. 4), adult female, collected by Antenor Leitão de Carvalho, in 1936. + + + +Type +locality. + +Municipality of Poção ( +08o11’S +, +36o42’W +, ca. +1035 m +a.s.l.), State of Pernambuco, Northeastern +Brazil +. + + + + +Diagnosis. +A species belonging to the + +Odontophrynus cultripes + +group and associated with the “caatinga” and “dry forest” environments (decidual and semi-decidual forests) of northeastern +Brazil +, is characterized by the following combination of traits: (1) size large (SVL 51.6–69.4 mm in males, 53.3–76.5 mm in females); (2) snout vertical in profile; (3) parotoid glands large, elongated to elliptical; (4) glands on forearms and tibiae absent; (5) dorsum with scattered, shallow glands; (6) elongated gland on the ventrolateral surface of forearm poorly developed; (7) elongated gland along the external border of the tarsus/metatarsus poorly developed; (8) foot webbing formula +I 1 +½–2+ +II 1 +½–3+ +III 2 +⅔– +3 IV +vestigial V. + + +Comparisons with other species. + +Odontophrynus carvalhoi + +is distinguished from + + +O +. cultripes + + +by the elongated to elliptical parotoid glands (ovoid in + + +O +. cultripes + + +), presence of shallow glands scattered on dorsum (absent or few in + + +O +. cultripes + + +), absence of a differentiated, large gland on the forearm (present in + + +O +. cultripes + + +), elongated gland on the ventrolateral surface of the forearm poorly developed (absent in + + +O +. cultripes + + +), absence of a conspicuous globose gland on the tibiae (present in + + +O +. cultripes + + +), and elongated gland along the external border of the tarsus/metatarsus poorly developed (conspicuous in + + +O +. cultripes + + +). From + + +O +. monachus + + + +sp. nov. + +, + + +O +. carvalhoi + + +is separated by the snout vertical in profile (obtuse in + + +O +. monachus + + + +sp. nov. + +), parotoid glands elongated to elliptical (globose, pearl +- +shaped in + + +O +. monachus + + + +sp. nov. + +), presence of shallow glands scattered on dorsum (absent in + + +O +. monachus + + + +sp. nov. + +), and foot webbing less developed (webbing formula in + + +O +. cultripes + + +, +I 1 +½–2+ +II 1 +½–3+ +III 2 +⅔– +3 IV +vestigial V; in + + +O +. monachus + + + +sp. nov. + +, +I 1–2 II 1–2 III 1–3 ++ +IV 3–1 +V). + + + + +FIGURE 4. + +Odontophrynus carvalhoi + +, holotype, MNRJ 0 313, adult female, SVL 63.3 mm, from the Municipality of Poção, State of Pernambuco, Brazil. + + + + +Description. +Body stout (fig. 5); head wider than long, HL about 74% of HW, HL about 32% of SVL, HW about 43% of SVL. Snout short, semi-circular viewed from above (fig. 5 A), vertical in profile (fig. 5 C); canthus rostralis distinct, rounded; loreal region oblique, slightly concave. Nostrils closer to tip of snout than to eyes; internarial distance slightly smaller than eye to nostril distance and much smaller than eye diameter. Eyes prominent, lateral, slightly directed ahead; eye to nostril distance much smaller than eye diameter, upper eyelid width, and interorbital distance. Upper eyelid width smaller than interorbital distance. Tympanum concealed. Upper eyelid, head, dorsal skin, and dorsal surface of thighs rugose, with small tubercles uniformly distributed; shallow glands scattered on dorsum, without forming defined pattern. Postorbital glands evident, small, approximately rounded; temporal glands present, about the same size as postorbitals, sometimes masqueraded by color pattern; parotoid glands large, elongated to elliptical; forearm and tibial glands absent. Flanks and ventral skin barely rugose; lateral skin adhered to the middle of the arm; belly disk fold indistinct; a granular seat patch under thighs. Vocal sac developed, subgular. Vocal slits present, amply opened along the sides of tongue; vomerine teeth in two small transverse series, almost contacting medially, laying between the relatively large choanae; tongue large, approximately circular, largely notched behind. Hand (fig. 5 E) with fingers slender, not webbed nor ridged, tips rounded, not expanded; fingers lengths IV <II <I <III, first finger slightly longer than second; subarticular tubercles large, rounded, the proximals more developed than distals; numerous rounded supernumerary tubercles present; outer metacarpal tubercle large, longitudinally divided, the outer part about two to three times the inner part; inner metacarpal tubercle elliptical, about half of outer; nuptial pads on thumbs and prepollex absent; a weak, elongated gland on the ventrolateral surface of the forearm; skin on forearm, hands, and fingers smooth. Legs short, tibia length smaller than thigh length; sum of tibia and thigh lengths approximately 75% of SVL. Foot large (fig. 5 D), foot length larger than tibia and thigh lengths, about 60% of SVL. Toes slender, not fringed; toes lengths I <II <V <III <IV; toe tips rounded; webbing formula +I 1 +½–2+ +II 1 +½–3+ +III 2 +⅔– +3 IV +vestigial V; subarticular tubercles large, rounded; sole of foot with distinct, approximately aligned, supernumerary tubercles; outer metatarsal tubercle very small, rounded; inner metatarsal tubercle very large, shovel-like, with the free external border keratinized; inner tarsal fold distinct, approximately the length of the tarsus; a weak, elongated gland along the external border of the tarsus/metatarsus; skin on feet and toes smooth. + + + +FIGURE 5. + +Odontophrynus carvalhoi + +, MNRJ 50203, adult male, SVL 57.4 mm, from the Municipality of Maracás, State of Bahia, Brazil. Dorsal (A) and ventral (B) views; head profile (C); ventral views of foot (D) and hand (E). + + + + +FIGURE 6. +Living specimen of + +Odontophrynus carvalhoi + +, UFBA 7350, adult male, SVL 61.8 mm, from the Parque Estadual das Sete Passagens, Serra de Jacobina mountain (a regional designation of the Serra do Espinhaço mountain range), Municipality of Miguel Calmon, State of Bahia, Northeastern Brazil (Photos by Rafael O. Abreu: 19 February 2007). + + + + +Measurements of +holotype +(mm). + +SVL 63.3; HL 22.9; HW 29.6; +IND +5.4; +END +5.3; ED 7.5; UEW 6.0; IOD 6.7; HAL 17.5; THL 26.6; TL 23.3; FL 38.8. + + +Color in life. +The following description was based on two adult males and one adult female from Maracás, State of Bahia, +Brazil +(fig. 6, specimens not identified, but currently housed in UFBA collection). Dorsal ground color grayish green. Dorsum with a blackish to grayish green Y-shaped mark, from each upper eyelid to near the sacral region, bordered and defined on outside by grayish white bands of similar width and extension, clearly to poorly evident, which may be continuous with a grayish thin to wide mid-dorsal stripe over the sacrum. Parotoid, temporal, and postorbital glands dark brown, each one delimited by a black edge; other minor glands and enlarged warts cream to dark brown with or without black edgings. Flank marked by a broad grayish white dorsolateral stripe from the parotoid gland to near the groin. Head highlighted by the anterior border of the dorsal Y-shaped mark, which outlines a V-shaped inter-ocular grayish white bar with black edges. Snout marked by the presence of two blackish brown stripes from upper lip to nostrils, continuing until reaching the anterior corner of eyes, delimiting a cross-shaped mask filled with dorsal background color. An additional three to four blackish brown perpendicular stripes present on the upper lip, a pale one placed in the midpoint between nostril and anterior corner of eye and the remaining three from anterior to posterior corners of eye, over a cream to somewhat orange background color. Arms and legs with irregular light to dark brown crossbars, which become less distinct proximally. Upper arms and forearms sometimes with thin orange longitudinal glandular stripes. Belly grayish white. Sole of foot and tarsus dark gray, with light gray tubercles. Superior and inferior surfaces of iris white; anterior and posterior surfaces blackish brown; a thin vertical black stripe divides the eye, the lower half larger than the upper half. + + +A male from the Parque Estadual das Sete Passagens, Municipality of Miguel Calmon, State of Bahia, +Brazil +(UFBA 7350) varied in color pattern, as follows: the grayish green background color observed in the Maracás specimens only was noted on surfaces of arms, legs, and flanks; light dorsal markings cream (instead of grayish white); and background color of dorsum brown (instead of grayish green). A longitudinal brown stripe on outer surfaces of forearm and tibia was present. Additional color data obtained from specimen UFBA 7350: chest and throat greenish brown; ventral surfaces of arms, hands, thighs, tibia, tarsus, and foot dark purple, with tubercles and skin glands white. + + +Color in preservative. +Follows the color in life, but with faded dorsal background color, which becomes light brown (grayish brown in live specimens). The ventral surfaces of arms, legs, feet, and hands become light brown; tubercles and ventral surfaces of fingers and toes become cream. + + +Variation. +Other examined specimens are congruent respecting the morphological characters and color. Sexual dimorphism is indicated by the presence of vocal sac in males and size slightly larger in females. Descriptive statistics of measurement data of males and females are in +Table 2 +. + + + +TABLE 2. +Descriptive statistics of the measurements (mm) of adult males and females of + +Odontophrynus carvalhoi + +. n, number of specimens; SD, standard deviation. Other abbreviations are defined in the text. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Characters SVL HL HW INDMales (n = 20) Range Mean 51.6–69.4 61.8 17.0–20.6 19.0 22.9–28.1 25.7 4.2–6.0 5.1SD 4.41 9.92 1.51 0.52Females (n = 6) Range Mean 53.3–76.5 67.9 19.9–23.2 22.1 25.4–32.8 29.2 4.9–6.1 5.5SD 9.01 1.17 2.62 0.42
END ED UEW IOD4.3–6.1 5.4 6.4–8.2 7.0 5.1–6.8 6.2 5.4–6.7 6.00.39 0.41 0.50 0.324.8–6.7 5.7 7.0–8.1 7.5 5.9–7.3 6.5 6.2–7.1 6.60.78 0.36 0.53 0.31
HAL THL15.2–20.0 18.2 20.7–28.4 25.11.45 1.7316.4–21.9 19.6 22.0–30.3 27.52.21 3.03
TL FL18.1–23.8 21.8 31.2–39.2 36.01.48 2.5619.8–26.3 23.7 33.2–45.4 40.12.42 4.31
+
+ +Advertisement call. +The following description was based on the advertisement call of a male from the Municipality of Maracás and a male from Serra do Ramalho, both in the State of Bahia, +Brazil +. The call (fig. 7 A–D) is composed by one multi-pulsed note. Pulses with highest peak intensities always localized around the middle of a note (fig. 7 B, C). Three main energetic bandwidths (sidebands) are distinguishable in the audiospectrogram (fig. 7 A, D), and possibly are due to the pulsatile nature of the call. Note with frequency modulation, rising to higher frequencies up to the first half of note, and then decreasing till the end of note. Detailed descriptive statistics is given in +Table 1 +. For comparisons with other species of the + + +O +. cultripes + + +group, see the + + +O +. monachus + + + +sp. nov. + +advertisement call description below. + + +Tadpole. +The tadpole was described and figured by +Caramaschi (1979) +. + + +Karyotype. +The karyotype was described and figured by +Beçak and Beçak (1970 +, +1974 +). + + +Geographic distribution and ecological remarks. + +Odontophrynus carvalhoi + +inhabits environments ca. +500 m +above sea level (fig. 3), mainly found in altitudes above +600 m +(70%). The species is geographically distributed between the Serra do Espinhaço mountain range (on west) and the Atlantic Ocean coastline (on east), from the Jequitinhonha river valley (on the south), in the State of Minas Gerais, up to State of Paraiba (on the north). The species occurs in the Caatinga biome (40% of geographic samples), in the Atlantic Forest biome (40%), and in the Cerrado biome (20%; see +Rizzini 1979 +for definitions of “Caatinga” and “Cerrado”). The Caatinga biome is characterized by a semi-arid to arid tropical or subtropical climate, covered by a super-xerophyte caatinga. This ecological scenario leads to a fallacious conclusion that + + +O +. carvalhoi + + +is a caatinga plant cover inhabitant. The species is often associated with deciduous or semideciduous forests (see +Silva & Casteleti 2005 +for distribution and characterization of the Tropical Atlantic Forest sub-regions: interior forests, São Francisco, Chapada +Diamantina, Brejos Nordestinos +, and west of the Espinhaço Mountain Range, within the São Francisco basin, along the margins of the São Francisco river). Only two samples were obtained within areas of sub-xerophyte caatinga, and another from an area of cerrado, but always adjacent to deciduous or semideciduous forest areas. Geographic samples of + + +O +. carvalhoi + + +are in three +types +of Köppen’s climate classification: Cwa (humid and sub-humid mesothermic climate; southern Bahia and northeastern Minas Gerais), megathermic humid and sub-humid climates (Aw, São Francisco river valley and Pernambuco State), and Am (Chapada Diamantina and adjacent areas). + +Odontophrynus carvalhoi + +can be considered a dry forest border inhabitant of northeastern +Brazil +. + +
+ + +Remarks. +The +holotype +of + +Odontophrynus carvalhoi + +is well preserved, only slightly fade. External characters, measurements, and body proportions have not changed from those given in the original description. + + +
+
\ No newline at end of file diff --git a/data/38/2A/87/382A87F70D15FFE688CB1AF22F812DFB.xml b/data/38/2A/87/382A87F70D15FFE688CB1AF22F812DFB.xml new file mode 100644 index 00000000000..2f1fa4aa154 --- /dev/null +++ b/data/38/2A/87/382A87F70D15FFE688CB1AF22F812DFB.xml @@ -0,0 +1,661 @@ + + + +Taxonomic revision of the Odontophrynus cultripes species group, with description of a new related species (Anura, Cycloramphidae) + + + +Author + +Caramaschi, Ulisses + + + +Author + +Napoli, Marcelo Felgueiras + +text + + +Zootaxa + + +2012 + +3155 + + +1 +20 + + + +journal article +45697 +10.5281/zenodo.212451 +ff28ec88-03cf-48a0-9798-d83735ab3d29 +1175-5326 +212451 + + + + + + + +Odontophrynus cultripes +Reinhardt and Lütken, 1862 + + + + + +Figure 1 + + + + + +Odontophrynus cultripes +Reinhardt and Lütken, 1862 + + +Pyxicephalus cultripes + +— +Cope, 1863 + + + +Ceratophrys cultripes + +— +Boulenger, 1882 + + + +Syntypes +. + +Zoologisk Museum, University of Copenhagen, +Denmark +(ZMUC) and [on exchange from ZMUC] Naturhistorische Museum, Wien, +Austria +(NHMW 16522), according to +Häupl and Tiedemann (1978) +and +Frost (2011) +. + + + + + +Type +locality. + +“Reinhardt har taget de 2 foreliggende Exemplarer ved Tamburil, en Landeiendom ikke langt fra Lagoa Santa, og ved Taboleiro Grande, en lille Flaekke beliggende en 12 Mill N. V. for nysnaevnte By” ( +Reinhardt & Lütken 1862 +) [“Reinhardt has taken the 2 available specimens at Tamburil, a ranch not far from Lagoa Santa, and at Taboleiro Grande, a small township lying about +12 miles +north west of the same city.”; translated by A. Schmidt-Nielsen]. Both localities referred by +Reinhardt and Lütken (1862) +, Tamburil and Taboleiro Grande (currently Derrubadas, according to +Bokermann 1966 +), are located in the Municipality of Lagoa Santa ( +19o38’S +, +43o54’W +, ca. +740 m +a.s.l.), State of Minas Gerais, +Brazil +. + + + + +Diagnosis. +A species belonging to the + +Odontophrynus cultripes + +group and associated with the Cerrado environments of Central and Southeastern +Brazil +, is characterized by the following combination of traits: (1) size large (SVL +50–60 mm +in males, +45–70 mm +in females); (2) snout vertical in profile; (3) parotoid glands large, ovoid; (4) glands on forearms and tibiae present; (5) dorsum without or with few scattered glands; (6) elongated gland on the ventrolateral surface of forearm present; (7) elongated gland along the external border of the tarsus/metatarsus present; (8) foot webbing formula +I 1 +½–2+ +II 1 +½–3+ +III 2 +⅔– +3 IV +vestigial V. + + +Comparisons with other species. + +Odontophrynus cultripes + +is distinguished from + + +O +. carvalhoi + + +and + + +O +. monachus + + + +sp. nov. + +by the ovoid parotoid glands (elongated to elliptical in + + +O +. carvalhoi + + +; globose, pearl-shaped in + + +O +. monachus + + + +sp. nov. + +), presence of a differentiated, large gland on the forearm (absent in + + +O +. carvalhoi + + +and + + +O +. monachus + + + +sp. nov. + +), presence of a conspicuous, globose gland on the tibiae (poorly developed in + + +O +. carvalhoi + + +and + + +O +. monachus + + + +sp. nov. + +), and presence of an elongated gland along the external border of the tarsus/metatarsus (poorly developed in + + +O +. carvalhoi + + +and + + +O +. monachus + + + +sp. nov. + +) Additionally, + + +O +. cultripes + + +is separated from + + +O +. carvalhoi + + +by the total absence or presence of few scattered glands on dorsum (presence of shallow glands scattered on dorsum of + + +O +. carvalhoi + + +), and from + + +O +. monachus + + + +sp. nov. + +by the vertical snout in profile (obtuse in + + +O +. monachus + + + +sp. nov. + +), and foot webbing less developed (foot webbing formula in + + +O +. cultripes + + +, +I 1 +½–2+ +II 1 +½–3+ +III 2 +½– +3 IV +vestigial V; in + + +O +. monachus + + + +sp. nov. + +, +I 1–2 II 1–2 III 1–3 ++ +IV 3–1 +V). + + + + +FIGURE 1. +Living specimen of + +Odontophrynus cultripes + +, MZUFV 6669, SVL 62,6 mm, adult male, from the Serra do Brigadeiro, Municipality of Araponga, State of Minas Gerais, Brazil (Photo by Renato N. Feio: December 2005). + + + + +Description. +The species was well characterized by +Cochran (1955) +, +Savage and Cei (1965) +, and +Cei (1980) +, which makes unnecessary a redescription. + + +Color in life. +The following description was based on color photographs of an adult male from Araponga, State of Minas Gerais, +Brazil +(MZUFV 6669), and another from Viçosa, State of Minas Gerais, +Brazil +(not collected). Dorsal ground color grayish green. A weak thin dorsal black to blackish brown Y-shaped mark is discernible from each upper eyelid to near the posterior edges of parotoid glands, bordered and defined on outside by broad reddish cream bands of similar width and extension. A reddish cream mid +- +dorsal pin stripe is visible over the sacrum. Parotoid, temporal, and postorbital glands reddish brown, each one delimited by a black edge; other minor glands and enlarged warts orange to greenish brown with or without black edgings. Flank marked by a broad reddish cream dorsolateral stripe from the parotoid gland to near the groin. Head highlighted by the anterior border of the dorsal Y-shaped mark, which outlines a V-shaped interocular reddish cream bar with dark brown edges. Snout marked by the presence of two blackish brown stripes from upper lip to nostrils, and posteriorly until reaching the anterior corner of eyes, delimiting a cross-shaped mask filled with dorsal background color. Three to four other blackish brown perpendicular stripes were present on the upper lip, a pale one placed in the midpoint between nostril and anterior corner of eye, and the remaining three from anterior to posterior corners of eye, on a cream to somewhat orange background. Arms and legs with irregular light to dark brown crossbars, which become less distinct proximally. Tibial gland reddish brown. Forearms with a well developed orange longitudinal glandular stripe. Belly grayish white; throat greenish brown. Sole of foot and tarsus dark gray, with light gray tubercles. Superior and inferior surfaces of iris white, marbled with thin black reticulations; anterior and posterior surfaces black; a thin vertical black stripe divides the eye, the lower half larger than the upper half, which may be absent. + + +Color in preservative. +Dorsum of head, body, and limbs brownish or olive-brown; a cream interorbital bar; sides of head light brown with two dark brown blotches, one below and the other in front of the eye; two distinct cream stripes on the body sides, running obliquely downward from the tympanic area nearly to groin; a short middorsal whitish-cream line on the sacrum; arms and legs with irregular light and dark brown crossbars, becoming less distinct proximally; glands and enlarged warts brown with some black edging. Undersurfaces uniformly cream; throat of males grey to dark brown. + + +Advertisement call. +The following description is based on the advertisement calls of two males from the Municipality of +São Tomé +das Letras, State of Minas Gerais, +Brazil +. The call (fig. 2 A–D) is composed by one multi-pulsed note. Four main energetic bandwidths (sidebands) are distinguishable in the audiospectrogram (fig. 2 A, D), due to the pulsatile nature of the call. Pulses with the highest energy peaks arise in the first half of note (fig. 2 C, D). Detailed descriptive statistics are given in +Table 1 +. For comparisons with other species of the + + +O +. cultripes + + +group, see the + + +O +. monachus + + + +sp. nov. + +advertisement call description below. + + +FIGURE 2. +(A) audiospectrogram, (B) oscillogram, (C) oscillogram of the first note, and (D) power spectrum of the advertisement call of + +Odontophrynus cultripes + +from the Municipality of +São Tomé +das Letras, State of Minas Gerais, +Brazil +. Air temperature 14o C. + + +Tadpole. +The tadpole was described and figured by +Savage and Cei (1965) +and +Cei (1980) +. + + +Karyotype. +The karyotype was described and figured by + +Beçak +et al. +(1967 + +, +1971 +), +Beçak and Beçak (1974) +, +Ruiz and Beçak (1976) +, and + +Ruiz +et al. +(1981) + +. + + +Geographic distribution and ecological remarks. +The geographical distribution of + + +O +. cultripes + + +is mapped in fig. 3. + +Odontophrynus cultripes + +mainly inhabits environments of altitudes higher than +800 m +a.s.l. ( +800–999 m +: 61.4% of the total number of localities, n = 67;> +1000 m +: 19.3%; +600–799 m +: 15.8%; +500–599 m +: 3.5%). The southern limit of the species distribution is defined by the southern sector of the Serra da Mantiqueira mountain range; the eastern limit is defined by the Serra do Espinhaço mountain range, except by three samples located in the northern sector of the Serra da Mantiqueira mountain range. From its southernmost to northernmost distribution limits (Central Brazilian Plateau), + + +O +. cultripes + + +is distributed through a series of plateaus and mountain chains in the states of Minas Gerais and Goiás (Serra da Canastra, Planalto Central Brasileiro, Planalto Centro Sul de Minas, and Patamares and Serras do Rio São Francisco; see + +Alvarenga +et al +. 1997 + +for definition of Brazilian relief units). Most known populations of + + +O +. cultripes + + +are under a Cwa +type +of Köppen’s climate classification (humid and sub-humid mesothermic climate) and less frequently under a Cwb or Cfa +types +. The north-westernmost known population samples of the species are located in the Cerrado biome (see +Rizzini 1979 +for definition of “Cerrado”), whereas southernmost samples are in the Tropical Atlantic Forest biome, inhabiting seasonal semi-deciduous forests (known as interior forests; see +Silva & Casteleti 2005 +for distribution and characterization of the Tropical Atlantic Forest sub-regions). We do not have ecological data from all geographic samples, but + + +O +. cultripes + + +may be associated with semideciduous or deciduous forest borders within the Cerrado biome, as occurs to + + +O +. carvalhoi + + +within the Caatinga biome (see below). + + + +TABLE 1. +Acoustic properties of the advertisement call of + +Odontophrynus carvalhoi + +(Maracás and Serra do Ramalho, State of + + + +Bahia, +Brazil +), + + +O +. cultripes + + +( +São Tomé +das Letras, State of Minas Gerais, +Brazil +), and + + +O +. monachus + + +( +holotype +, Parque Nacional + + +da Serra da Canastra, State of Minas Gerais, +Brazil +). Values are: mean ± standard deviation (range; sample size). +n +, number of + +specimens analyzed. Temporal parameters of the call in seconds. Frequencies in kilohertz (kHz). Values in bold indicate main +differences among species. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+ +O. carvalhoi + + + +O. cultripes + +( +n += 2) + + +O. monachus + +( +n += 1) +
+Maracás ( +n += 1) + +Serra do Ramalho ( +n += 2) +
Call duration0.31 ± 0.01 (0.24–0.35; 96)0.39 ± 0.09 0,34 ± 0.04 (0.26–0.50; 22) (0.27–0.40; 30)0.62 ± 0.18 (0.28–0.98; 54)
Interval between calls1.35 ± 0.38 (0.75–2.51; 96)2.36 ± 1.05 2.68 ± 0.88 (1.27–4.51; 22) (1.62–4.90; 24)1.49 ± 0.60 (0.72–3.91; 36)
Number of notes11 11–3 (mode 2)
Note duration (overall)0.31 ± 0.01 (0.24–0.35; 96)0.39 ± 0.09 0,34 ± 0.04 (0.26–0.50; 22) (0.27–0.40; 30)0.31 ± 0.03 (0.23–0.39; 54)
Note 1 duration0.31 ± 0.01 (0.24–0.35; 96)0.39 ± 0.09 0,34 ± 0.04 (0.26–0.50; 22) (0.27–0.40; 30)0.33 ± 0.02 (0.28–0.39; 54)
Note 2 duration— —0.28 ± 0.01 (0.23–0.34; 54)
Note 3 duration— —0.27 ± 0.01 (0.28; 2)
Inter–note duration1.35 ± 0.38 (0.75–2.51; 96)2.36 ± 1.05 2.68 ± 0.88 (1.27–4.51; 22) (1.62–4.90; 24)0.08 ± 0.02 (0.06–0.18; 54)
Note rate (notes/s)3.19 ± 0.20 (2.79–4.06; 96)2.72 ± 0.70 3.18 ± 0.18 (1.98–3.84; 22) (3.04–3.72; 30)2.88 ± 0.18 (2.50–3.52; 54)
Number of pulses29.41 ± 1.86 (23–34; 96)42.90 ± 10.06 23.21 ± 2.19 (30–54; 22) (19–28; 29)25.33 ± 2.70 (20–32; 54)
Note pulse rate (pulses/s)93.56 ± 1.79 (89.7–96.3; 96)110.17 ± 2.39 69.26 ± 2.41 (104.9–115.3; 22) (62.2–71.7; 29)80.91 ± 4.20 (73.3–92.7; 54)
Frequency amplitude0.42–0.710.40–0.78 0.42–0.780.42–0.81
Call dominant frequency0.50 ± 0.19 (0.48–0.59; 96)0.58 ± 0.03 0.66 ± 0.00 (0.47–0.60; 22) (0.66, 30)0.63 ± 0.05 (0.54–0.72; 54)
+
+ + +Remarks. +The specimens referred by +Cochran (1955) +as + +Odontophrynus cultripes + +to “Rio de Janeiro: Alto Itatiaia, AMNH 17060” and “São Paulo: Butantan, USNM +121326 +and IB 3.”, not examined by us, are probably + +Odontophrynus americanus + +, or the localities are in error; the specimens referred to “Rio Grande do Sul: Passo Fundo, IB 87–8 and USNM +121327 +”, not examined by us, are probably + +Odontophrynus maisuma + +, or the locality is in error. + + +
+
\ No newline at end of file diff --git a/data/38/2A/87/382A87F70D1BFFF388CB19E22E3B2891.xml b/data/38/2A/87/382A87F70D1BFFF388CB19E22E3B2891.xml new file mode 100644 index 00000000000..818ce77bcd4 --- /dev/null +++ b/data/38/2A/87/382A87F70D1BFFF388CB19E22E3B2891.xml @@ -0,0 +1,795 @@ + + + +Taxonomic revision of the Odontophrynus cultripes species group, with description of a new related species (Anura, Cycloramphidae) + + + +Author + +Caramaschi, Ulisses + + + +Author + +Napoli, Marcelo Felgueiras + +text + + +Zootaxa + + +2012 + +3155 + + +1 +20 + + + +journal article +45697 +10.5281/zenodo.212451 +ff28ec88-03cf-48a0-9798-d83735ab3d29 +1175-5326 +212451 + + + + + + + +Odontophrynus monachus + +sp. nov. + + + + +Figures 8–9 + + + +Odontophrynus +cf. +carvalhoi + +— +Haddad, Andrade and Cardoso, 1988 +. + + + + + +Holotype +: + +ZUEC +4440 (fig. 8), adult male, collected at Parque Nacional da Serra da Canastra ( +20o10'S +, +46o30'W +, ca. +1350 m +a.s.l.), headwaters of the São Francisco River, Municipality of São Roque de Minas, State of Minas Gerais, Southeastern +Brazil +, on +13 October 1981 +, by A.J. Cardoso, G.V. Andrade and C.F.B. Haddad. + + + +Paratypes +. + +MZUSP +132973–132974, males, +MZUSP +132972, female, collected at the +type +locality in +December 2004 +, by C. Nogueira. + + + + +Diagnosis. +A species belonging to the + +Odontophrynus cultripes + +group by having a single, greatly developed, smooth, parotoid gland, no enlarged glands on back and sides, except by well-developed postorbital and temporal glands, and presence of a glandular fold on the posterior surface of forearm; it is characterized by the following combination of traits: (1) size small (SVL 40.6–54.1 mm in males, 55.5 mm in female); (2) snout obtuse in profile; (3) parotoid glands globose, pearl-shaped; (4) glands on forearms and tibiae absent; (5) dorsum granulose, without scattered glands; (6) elongated gland on the ventrolateral surface of forearm poorly developed; (7) elongated gland along the external border of the tarsus/metatarsus poorly developed; (8) webbing formula, +I 1–2 II 1–2 III 1–3 ++ +IV 3–1 +V. + + +Comparisons with other species. + +Odontophrynus monachus + + +sp. nov. + +is distinguished from + + +O +. carvalhoi + + +and + + +O +. cultripes + + +by the larger head (HL 33% of SVL, HW 44.3% of SVL in + + +O +. monachus + + + +sp. nov. + +; HL 31% of SVL, HW 42% of SVL in + + +O +. carvalhoi + + +; HL 30% of SVL, HW 40.5% of SVL in + + +O +. cultripes + + +), snout profile obtuse (vertical in + + +O +. carvalhoi + + +and + + +O +. cultripes + + +), and foot webbing more extensive (webbing formula, +I 1–2 II 1–2 III 1– 3 ++ +IV 3–1 +V in + + +O +. monachus + + + +sp. nov. + +; +I 1 +½–2+ +II 1 +½–3+ +III 2 +⅔– +3 IV +vestigial V in + + +O +. carvalhoi + + +; +I 1 +½–2+ +II 1 +½–3+ +III 2 +⅔– +3 IV +vestigial V in + + +O +. cultripes + + +). Additionally, + + +O +. monachus + + + +sp. nov. + +is separated from + + +O +. carvalhoi + + +by the globose, pearl–shaped parotoid glands (elongated to elliptical in + + +O +. carvalhoi + + +), and by the absence of scattered glands on dorsum (present in + + +O +. carvalhoi + + +); from + + +O +. cultripes + + +, the new species is distinguished by the absence of developed glands on forearms and tibiae, and by the poorly developed elongated glands on the ventrolateral surface of forearm and along the external border of the tarsus/metatarsus (conspicuous in + + +O +. cultripes + + +). + + + + + +Description of +holotype +. + +Body stout (fig. 8); head wider than long, HL 74.4% of HW, HL 33% of SVL, HW 44.3% of SVL. Snout short, semi-circular viewed from above (fig. 9 A), obtuse in profile (fig. 9 B); canthus rostralis distinct, canthal crest present; loreal region oblique, slightly concave. Nostrils approximately at the same distance from tip of snout as from eyes; internarial distance slightly larger than eye to nostril distance and much smaller than eye diameter. Eyes large, prominent, lateral, slightly directed ahead; eye to nostril distance much smaller than eye diameter and upper eyelid width, and slightly larger than interorbital distance. Upper eyelid width larger than interorbital distance. Tympanum concealed. Upper eyelid, head, dorsal skin, and dorsal surface of thighs rugose, with small tubercles uniformly distributed. Postorbital gland large, approximately pearl-shaped; temporal gland large, slightly smaller than postorbital; parotoid gland large, globose, pearl-shaped; forearm and tibial glands absent. Flanks and ventral skin barely rugose; lateral skin adhered to the middle of the arm; belly disk fold indistinct; a granular seat patch under thighs. Vocal sac developed, subgular. Vocal slits present, amply opened along the sides of tongue; vomerine teeth in two small transverse series, almost contacting medially, laying between the relatively large choanae; tongue large, approximately circular, notched behind. Hand (fig. 9 C) with fingers slender, not webbed nor ridged, tips rounded, not expanded; fingers lengths IV <II <I <III, first finger longer than second; subarticular tubercles large, rounded, the proximals more developed than distals; several rounded supernumerary tubercles present; outer metacarpal tubercle large, longitudinally divided, the outer part about three times the inner part; inner metacarpal tubercle large, rounded, slightly smaller than outer; nuptial pads on thumbs and prepollex absent; a weak, elongated gland on the ventrolateral surface of the forearm; skin on forearm, hands, and fingers smooth. Legs short, tibia length smaller than thigh length; sum of tibia and thigh lengths 73.2% of SVL. Foot large (fig. 9 D), foot length larger than tibia and thigh lengths, 59.6% of SVL. Toes slender, fringed; toes lengths I <II <V <III <IV; toe tips rounded; webbing formula, +I 1–2 II 1–2 III 1–3 ++ +IV 3–1 +V; subarticular tubercles large, rounded; sole of foot with distinct, approximately aligned, small supernumerary tubercles; outer metatarsal tubercle absent; inner metatarsal tubercle very large, shovel-like, with the free external border keratinized; inner tarsal fold distinct, approximately the length of the tarsus; a weak, elongated gland along the external border of the tarsus/metatarsus; skin on feet and toes smooth. + + + +Measurements of +holotype +. + +See +Table 3 +. + + + +TABLE 3. +Measurements (mm) of adult males and female from the type-series of + +Odontophrynus monachus + + +sp. nov. + +Abbreviations are defined in the text. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
ZUEC 4440 HolotypeMZUSP 132974 MZUSP 132973 Paratype ParatypeMZUSP 132972 Paratype
CharactersMalesFemale
SVL40.648.8 54.155.5
HL13.415.5 17.616.3
HW18.020.1 24.124.0
IND3.54.8 4.85.2
END3.45.2 5.34.9
ED5.85.9 6.46.1
UEW5.05.0 6.15.3
IOD3.34.9 4.96.4
HAL11.013.9 15.814.4
THL15.519.9 22.920.3
TL14.217.8 20.620.0
FL24.231.7 34.534.4
+
+ +Color in preservative. +Dorsum of head, body, and limbs brown or olive-brown; a cream interorbital bar; sides of head light brown with two dark brown blotches, one below and the other in front of the eye; two distinct cream stripes on the body sides, running obliquely downward from the tympanic area nearly to groin; a short mid-dorsal whitish-cream line on the sacrum; arms and legs with irregular light and dark brown crossbars, becoming less distinct proximally; glands and enlarged warts brown with some black edging. Undersurfaces uniformly clear-cream; throat of males grey to dark brown. + + +Variation. +Examined specimens not vary from the above descriptions. Sexual dimorphism is indicated by the presence of vocal sac in males and slightly larger size in females. Measurements of +paratypes +are in +Table 3 +. + + +Advertisement call. +The following description is based on 54 advertisement calls of the +holotype +from the Parque Nacional da Serra da Canastra, Municipality of São Roque de Minas, State of Minas Gerais, +Brazil +. The call (fig. 10 A–D) is composed by 1 (14 calls, 25.9%), 2 (38 calls, 70.4%), or 3 (2 calls, 3.7%) multi-pulsed notes. Three main energetic bandwidths (sidebands) are distinguishable in the audiospectrogram (fig. 10 A, D), due to the pulsatile nature of the call. Pulses with the highest energy peaks occur at the end of the note (fig. 10 B, C). Modest frequency modulation occurs at the end of notes, rising to higher frequencies. Detailed descriptive statistics are given in +Table 1 +. + + +The advertisement calls of + + +O +. carvalhoi + + +and + + +O +. cultripes + + +are readily diagnosed from those of + + +O +. monachus + + +by having a single note (1–3 notes in the latter, but each call often contains 1–2 notes). Inter-note duration in the call of + + +O +. monachus + + +is very short (0.06– +0.18 s +), much longer in + + +O +. carvalhoi + + +(0.75– +4.51 s +) and + + +O +. cultripes + + +(0.28– +0.61 s +). The note pulse rate in + + +O +. cultripes + + +(62.2–71.7 pulses/s) is less than that of + + +O +. carvalhoi + + +and + + +O +. monachus + + +(combined note pulse rate 73.3–115.3 pulses/s). In addition, the waveform structure of a note of + + +O +. monachus + + +clearly differs from + + +O +. carvalhoi + + +and + + +O +. cultripes + + +by presenting pulses with the highest energy peaks at the end of the note, while in the other two species the highest energy peaks are around the middle of the note. + + +Tadpole. +Unknown. + + +Karyotype. +Unknown. + +
+ + +Etymology. +The specific epithet, “ + +monachus + +”, is a Latin masculine substantive used in apposition, meaning “monk”, in allusion to the followers of Saint Francis of Assis, the Franciscan monks. Saint Francis was born on + +26 September +1181 + +in Assis, +Italy +, and died on 0 +3 October 1226 +, also in Assis. He was canonized in 1228 and currently Saint Francis of Assis is known as patron of the animals and of the environment. The name is given for the +type +locality, in the headwaters of the São Francisco River. + + + +FIGURE 8. + +Odontophrynus monachus + + +sp. nov. + +, holotype, ZUEC 4440, adult male, SVL 40.6 mm, from the Parque Nacional da Serra da Canastra, Municipality of São Roque de Minas, State of Minas Gerais, Brazil. Dorsal (A) and ventral (B) views. + + + + +FIGURE 9. + +Odontophrynus monachus + + +sp. nov. + +, holotype, ZUEC 4440, adult male, SVL 40.6 mm, from the Parque Nacional da Serra da Canastra, Municipality of São Roque de Minas, State of Minas Gerais, Brazil. Dorsal (A) and lateral (B) views of head; ventral views of hand (C) and foot (D). + + + +Geographic distribution and ecological remarks. +Known only from the +type +locality (fig. 3), in the Parque Nacional da Serra da Canastra, southwestern State of Minas Gerais, southeastern +Brazil +. + + +According to IBAMA (1997), the Parque Nacional da Serra da Canastra was established on 0 +3 April 1972 +, comprising areas of the municipalities of São Roque de Minas, Sacramento, and Delfinópolis, in southwestern State of Minas Gerais, +Brazil +. The regional climate is classified as tropical, humid heat, with four or five dry months (normally May to September). The annual average temperature ranges between 18–20o C, with absolute maximum of 34–36o C and absolute minimum of -4–0o C. The annual rainfall is between + +1500 and +1750 + +mm a year. In the predominantly rolling relief of the National Park are the main headwaters of two important rivers, the São Francisco and the Araguari Rivers. + + +FIGURE 10. +(A) audiospectrogram, (B) oscillogram, (C) oscillogram of the first note of the second call, and (D) power spectrum of the advertisement call of + +Odontophrynus monachus + + +sp. nov. + +, +holotype +, ZUEC 4440, from the Parque Nacional da Serra da Canastra, Municipality of São Roque de Minas, State of Minas Gerais, +Brazil +. Air temperature 18o C; water temperature 19o C. Interval between calls is abbreviated in the figure. + + + +Haddad +et al. +(1988) + +stated that the specimen ZUEC 4440, here the +holotype +of + + +O +. monachus + + + +sp. nov. +, + +was collected in the area around the two main riverheads of the São Francisco River, above the landmark of these riverheads, at approximately +1350 m +a.s.l. The area had many swamps covered by grasses on dark, clayish soil, with small, slow rivulets and pools formed in its beds. Specimens of + + +O +. monachus + + + +sp. nov. + +were observed near shallow temporary pools or on the border of pools formed in the rain drainage beds. In these sites, males start calling at dusk. In the same area a putative also new species was collected and treated as “ + +Odontophrynus + +sp. ( + +aff. +moratoi +Jim & Caramaschi, 1980 + +)”. Other anuran species obtained in the same area were + +Bufo rufus +Garman + +[currently + +Rhinella rubescens +(A. Lutz) + +], + +Hyla albopunctata +Spix + +(= + +Hypsiboas albopunctatus + +), + +H. canastrensis +Cardoso & Haddad + +(= + +Scinax canastrensis + +), + +H. cipoensis +B. Lutz + +(= + +Hypsiboas cipoensis + +), + +H. ibitiguara +Cardoso + +(= + +Bokermannohyla ibitiguara + +), + +H. machadoi +Bokermann & Sazima + +(= + +Scinax machadoi + +), + +H. maracaya +Cardoso & Sazima + +(= + +Scinax maracaya + +), + +H. minuta +Peters + +(= + +Dendropsophus minutus + +), and + +H. squalirostris +A. Lutz + +(= + +Scinax squalirostris + +), + +Crossodactylus +cf. +trachystomus +(Reinhardt & Lütken) + +, + +Leptodactylus cunicularius +Sazima & Bokermann + +, + +L. furnarius +Sazima & Bokermann + +, + +L. jolyi +Sazima & Bokermann + +(currently + +L. sertanejo +Giaretta + +& Costa), + +L. labyrinthicus +(Spix) + +, + +Physalaemus cuvieri +Fitzinger + +, and + +Pseudopaludicola saltica +(Cope) + +. + + + + +Remarks. +The distinctiveness of + +Odontophrynus monachus + + +sp. nov. + +was first observed by + +Haddad +et al. +(1988) + +, by indicating that the collected specimen (the +holotype +) showed characters that ally it to + + +O +. carvalhoi + + +, but pronounced differences were also noted, mainly relating to total length and dorsal glands distribution. However, they refrained to from further taxonomic action pending the acquisition of additional data on different populations of + + +O +. carvalhoi + + +. + + +
+
\ No newline at end of file diff --git a/data/38/2A/9D/382A9D7BDFDD5EE6B5238D068DC4F31D.xml b/data/38/2A/9D/382A9D7BDFDD5EE6B5238D068DC4F31D.xml new file mode 100644 index 00000000000..b7fb580a97f --- /dev/null +++ b/data/38/2A/9D/382A9D7BDFDD5EE6B5238D068DC4F31D.xml @@ -0,0 +1,159 @@ + + + +Two new species and a new species record of Aglaia (Meliaceae) from Indonesia + + + +Author + +Pannell, Caroline M. +University of Oxford, Department of Plant Sciences and Daubeny Herbarium (FHO), South Parks Road, Oxford OX 1 3 RB, United Kingdom & Royal Botanic Gardens, Kew (K), Richmond, Surrey TW 9 3 AE, United Kingdom & Queen's University Belfast, Marine Laboratory, 12 - 13 The Strand, Portaferry, County Down, BT 22 1 PF, United Kingdom & Leipzig University, Institute of Biology, Department of Molecular Evolution and Plant Systematics & Herbarium (LZ), Johannisallee 21 - 23, D- 04103 Leipzig, Germany + + + +Author + +Schnitzler, Jan +Leipzig University, Institute of Biology, Department of Molecular Evolution and Plant Systematics & Herbarium (LZ), Johannisallee 21 - 23, D- 04103 Leipzig, Germany + + + +Author + +Muellner-Riehl, Alexandra N. +Leipzig University, Institute of Biology, Department of Molecular Evolution and Plant Systematics & Herbarium (LZ), Johannisallee 21 - 23, D- 04103 Leipzig, Germany & German Centre for Integrative Biodiversity Research (iDiv) Halle-Jena-Leipzig, D- 04103 Leipzig, Germany +https://orcid.org/0000-0002-2710-469X +muellner-riehl@uni-leipzig.de + +text + + +PhytoKeys + + +2020 + +155 + + +33 +51 + + + + +http://dx.doi.org/10.3897/phytokeys.155.53833 + +journal article +http://dx.doi.org/10.3897/phytokeys.155.53833 +1314-2003-155-33 +484AACC0E49956DC8FC9EEE295B4799E + + + + +1. +Aglaia monocaula Pannell +sp. nov. +Fig. 1 + + + +Diagnosis. + + +Aglaia monocaula + +resembles + +Aglaia flavida + +, from which it differs through being a smaller, unbranched tree with reticulation subprominent and no indumentum on the lamina of the lower surface of the leaflets. It is unique in the genus in having a dark blackish-brown, slightly swollen, region at the base of the petiolules. + + + +Figure 1. + +Aglaia monocaula + +Pannell +A +habit +B +detail of lower surface of the leaflet +C +apical shoot subtending infructescence in a leaf axil +D +part of the infructescence with fruits cut transversely to show the three seeds and longitudinally to show the junction between the two peltate cotyledons typical of the genus + +Aglaia + +(Drawn by Rosemary Wise, edited by Alexandra Muellner-Riehl). + + + + +Holotype. + +Indonesia. +West Papua +: Kecamatan Ayfat, neighborhood of Ayawasi, fr. 12 Feb. 1995, +K. Yumte +126 (L) + + +Tree, 3-10 m high, +unbranched +, with a terminal tuft of spirally inserted leaves; bole 4 cm in diameter; latex white. Twigs greyish-brown with large orange-brown pustules, densely covered with orange-brown and dark brown compact stellate hairs at the apex, glabrescent on older wood. + +Leaves 47-70 cm long, 28-32 cm wide; petiole 11-30 cm long; the petiole, rachis and petiolules with few to numerous hairs like those on the twigs, glabrescent. Leaflets 15, the laterals opposite or subopposite, coriaceous, lamina 7-16 cm long 2-5.5 cm wide, elliptical, slightly up-curved at the margins, cuneate at the slightly asymmetrical base, tapering to an acuminate apex, the acumen obtuse and 10-12 mm long; lateral veins 5-14, ascending and curved upwards near the margin, not anastomosing, lateral veins and reticulation subprominent; midrib prominent below with sparse stellate scales, absent from lower leaflet surface, upper and lower leaflet surfaces minutely rugulose; petiolules 10-15 mm on lateral leaflets, slender, 20-40 mm long on terminal leaflet, all with a dark blackish-brown, slightly swollen, region at the base of the petiolules. +Inflorescences not seen. +Infructescence 11 cm long, 7 cm wide; peduncle 6 cm long, the peduncle and fruit stalks with few to numerous hairs like those on the twigs, glabrescent. Fruits 2.8 cm long, 1.8 cm wide, ovoid, pericarp bright scarlet or pinkish-red, inner pericarp white, dehiscent with three locules each containing 1 seed; seed white where attached to the central axis of the fruit by a large hilum, aril orange. + + +Distribution. +Known only from the area around Ayawasi village in West Papua. + + +Ecology. +Primary open forest on limestone ridge to 600 m, with an abundant growth of moss. Fruits eaten by kuskus. + + +Use. +Wood used for house beams. + + +Vernacular. +sapa sai (K.Yumte) + + +Etymology. + +The specific epithet of + +Aglaia monocaula + +refers to the unbranched habit of this small tree. + + + +Conservation. +This species is known from only two fruiting specimens collected near Ayawasi village and is therefore assessed to be Data Deficient (provisional). Further collecting and monitoring is necessary to allow more conclusive estimations about the rareness and vulnerability of the species. However, the collections seen were made 24 and 25 years ago, so the likelihood of obtaining further material from this species is not great. + + +Additional specimen. + +Indonesia. +West Papua +: top ridge of limestone hills south of Ayawasi village, fr., 1 May 1996, +Polak +1221 (FHO) + + + +Notes. +This new species is represented by two fruiting specimens of monocaul trees that have leaves with a long petiolule on the terminal leaflet. + + + \ No newline at end of file diff --git a/data/38/2A/A5/382AA562F47C806E4BB4FC1C232ECFD1.xml b/data/38/2A/A5/382AA562F47C806E4BB4FC1C232ECFD1.xml new file mode 100644 index 00000000000..b850dfaa058 --- /dev/null +++ b/data/38/2A/A5/382AA562F47C806E4BB4FC1C232ECFD1.xml @@ -0,0 +1,45 @@ + + + +A catalogue of the ants of Paraguay (Hymenoptera: Formicidae). + + + +Author + +Wild, A. L. + +text + + +Zootaxa + + +2007 + +1622 + + +1 +55 + + + + +http://www.antbase.org/ants/publications/21367/21367.pdf + +journal article +21367 + + + + +longinodis MacKay +2004. + + + +Alto Paraguay (INBP, MCZC, WPMC). Literature records: Alto Paraguay (MacKay 2004). + + + \ No newline at end of file diff --git a/data/38/2B/00/382B00939581C768BD24B4B0A614AB79.xml b/data/38/2B/00/382B00939581C768BD24B4B0A614AB79.xml new file mode 100644 index 00000000000..8b1c8b40d49 --- /dev/null +++ b/data/38/2B/00/382B00939581C768BD24B4B0A614AB79.xml @@ -0,0 +1,62 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Anomia crispa +[ +spec. nov. +] + + + +A. testa dilatato-triangulari plicata sulcis rugosis: media latiore. + +Mus. Tessin. p... t. +5. +f. +7. + + + + +Habitat .. fossilis. + + + + +Testa fere lunata, sed natis superior prominens. Sulci +5 +s. +6 +rugis arcuatis transversis. Latera testae +submucronata. + + + + \ No newline at end of file diff --git a/data/38/2B/15/382B15FD10A1E33E1A3F6746F4CEB84D.xml b/data/38/2B/15/382B15FD10A1E33E1A3F6746F4CEB84D.xml new file mode 100644 index 00000000000..fe8558707bd --- /dev/null +++ b/data/38/2B/15/382B15FD10A1E33E1A3F6746F4CEB84D.xml @@ -0,0 +1,43 @@ + + + +Abessinische und andere afrikanische Ameisen, gesammelt von Herrn Ingenieur Alfred Ilg, von Herrn Dr. Liengme, von Herrn Pfarrer Missionar P. Berthoud, Herrn Dr. Arth. Müller, etc. + + + +Author + +Forel, A. + +text + + +Mitteilungen der Schweizerischen Entomologischen Gesellschaft + + +1894 + +9 + + +64 +100 + + + +journal article +3950 +10.5281/zenodo.14259 + + + + +Pheidole crassinoda Emery +i. litt. + + + +Delagoa (Dr. Liengme). + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C974C9C37FF06FBF7FC660786.xml b/data/38/2B/5C/382B5C2C974C9C37FF06FBF7FC660786.xml new file mode 100644 index 00000000000..f4696fa52a6 --- /dev/null +++ b/data/38/2B/5C/382B5C2C974C9C37FF06FBF7FC660786.xml @@ -0,0 +1,319 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Lissodesmus grampianensis + +n. sp. + + + + + + +Fig. 33 +; map +Fig.12 + + + + +Holotype + +: +Male. Stoney Creek +, +Grampians National Park +, +Vic +, +37º08'56"S +142º28'30"E +, + +650 m + +, + +12 November 2005 + +, +R +. +Mesibov +, +T +. +Moule +& +R +. +van Riet. In +MV +, K-10647. + + + + + +Paratypes + +: +In +MV +: 1 stadium + + +7 male +, +Dairy Creek +, +Grampians National Park +, +Vic +, +37º11'01"S +142º30'30"E +, + +490 m + +, + +4 October 2005 + +, +R +. +Mesibov +& +T +. +Moule +, K-10642 + +; + +1 male +, +1 female +, location as for holotype but + +4 October 2005 + +, +R +. +Mesibov +& +T +. +Moule +, K-10643, 10644 + +; + +2 females +, ' +Wonderland' +, +Grampians National Park +, +Vic +, +37º08'44"S +142º30'09"E +, + +390 m + +, + +6 October 2005 + +, +R +. +Mesibov +& +T +. +Moule +, K-10645, 10646 + +; +1 male +, 2 stadium +7 males +, +4 females +, details as for +holotype +, K-10648–10654. + + + +In +AM +: +1 male + +, + +Mt William +, +Grampians National Park +, +Vic +, +37º15'36"S +142º34'06"E +, + +630 m + +, + +13 November 2005 + +, +R + +. + +Mesibov +, +T + +. + +Moule +& +R + +. + +van +Riet +; +KS +103043 + +. + + +Other material examined +: None available. + + +Diagnosis +: + +Lissodesmus sensu +Mesibov (2006) + +with the femoral process of the gonopod telopodite very long and thin, the tip curving medially and lying just under the slightly flexed tip of the prefemoral process. + + +Description +: Male/female approximate measurements: length 19/ +20 mm +, midbody vertical diameter 1.5/ +1.5 mm +, midbody width across paranota 2.0/2.0 mm. In alcohol, well-coloured specimens pale with sparse reddish mottling dorsally, denser mottling on paranota, on posterior edge of metatergites and along anterior edge of collum, with quadrangular red mark anteriorly and medially on vertex. + +Male with antennal sockets moderately impressed ventrolaterally, separated by about 1.5 X a socket diameter. Antenna short, barely reaching ring 3 when manipulated to extend backwards; relative length of antennomeres 2>(3,6)>(4,5), antennomere 6 widest. Collum slightly wider than head, narrower than tergite 2; sparsely setose anteriorly; anterior edge nearly straight in the middle, slightly convex laterally; posterior edge nearly straight, corners rounded. Rings 2–18 nearly equal in overall width. Waist well-defined, with faint longitudinal striations. Prozonites and metazonites smooth, transverse furrow only faintly indicated; limbus composed of long, narrow, flat tabs with irregularly toothed ends. Paranota smooth, swollen, wide (ratio of ring 12 overall width to prozonite width = 1.5); anterior shoulder broadly curved; lateral margin slightly thickened, slightly convex, slightly upturned, with 5–6 small notches each usually with one very short seta on anterior corner of notch; margin nearly straight in lateral view; posterior corner produced into broad tooth beginning ca. ring 9, teeth increasing in length from ring 9 to 19; posterior corner seta prominent. Ozopore small, opening dorsally and laterally close to paranotal margin and just anterior to base of posterior corner; pore formula 5, 7, 9, 10, 12, 13, 15–19. Spiracle nearly round, very slightly raised above pleural surface; anterior spiracle on diplosegments larger, posterior spiracle about midway between leg bases. Sternites very sparsely setose, slightly longer than wide; transverse impression deeper than longitudinal. Legs short, prefemur greatly swollen dorsally, femur somewhat swollen dorsally, both more so on anterior legs; most legs with postfemur and tibia expanded ventrodistally; relative podomere lengths tarsus>(prefemur, femur)>(postfemur, tibia) on anterior legs, femur>prefemur posteriorly; tarsus straight. On anterior legs, sphaerotrichomes on prefemur, femur, postfemur, tibia and tarsus, hemispherical with sharp-pointed, tapered setal shaft inclined distally and slightly outwards; brush setae on prefemur and femur, tapering with sharp-pointed tips. Pre-anal ring moderately setose; hypoproct trapezoidal; epiproct bluntly rounded, extending well past anal valves; 4 spinnerets in square array, all 4 within a shallow, low-walled cavity just below epiproct tip. + +Gonopore small, opening on rounded, mediodistal enlargement of leg 2 coxa. Gonopods extending to leg 4 bases when retracted; bases of legs 5, 6 and 7 well-separated, 4 less so. Aperture ovoid, wider than long, about two-thirds the width of the ring 7 prozonite, rim raised laterally. Gonocoxae small, bean-shaped, lightly joined posteromedially, with a few long setae on posterolateral surface. Telopodite ( +Fig. 33 +) long, straight, slender, setose on posterolateral surface to level of solenomere base. Using nomenclature as in +Mesibov (2006 +a): telopodite base nearly cylindrical; tibiotarsus arising at just under half the telopodite length on medial side, a little flattened anteroposteriorly, directed posteriorly at ca. 45º to long axis of telopodite and slightly medially, lateral edge serrate; solenomere arising just anterior and distal to tibiotarsus, a little flattened mediolaterally, bent posteriorly and medially parallel to tibiotarsus, with small backward-pointing process near tip on anterior edge; prefemoral process tapering at ca. two-thirds the telopodite length, curving medially, then laterally, bending slightly posteriorly, flattening and expanding near tip, the tip slightly flexed and twisted medially so lateral edge faces caudad, lateral edge produced into a comb of ca. 15 teeth; a small, notched uncus on posterior surface of prefemoral process at ca. one-third the length of process; femoral process arising on lateral side of telopodite just distal to solenomere base, process long, thin, subcylindrical, tapering very gradually, curving medially and posteriorly so tip lies just basal to tip of prefemoral process, two prominent, blunt teeth on anterior surface near tip, tip blunt. Cannula prominent; prostatic groove curving laterally, then medially on anterior surface of telopodite before joining base of solenomere, opening at solenomere tip. + +Female closely resembling male but very slightly larger, legs not swollen. Genital aperture with posterior margin slightly raised, centre further raised, rounded; cyphopods not examined. + +Distribution +: So far known only from wet sclerophyll forest at four sites from +390–650 m +on the eastern edge of Grampians National Park between Halls Gap and Mt William, a total area of ca. +50 km +2 +( +Fig. 12 +). In and under rotting logs. + + +Etymology +: For the Grampians, an isolated set of picturesque mountain ranges in western +Victoria +, home to this species. + + +Remarks +: + +L. grampianensis + +is substantially different in gonopod form from its nearest congener, + +L. catrionae + +, which occurs ca. +60 km +to the east on Mt Cole, and both species differ significantly from the co-occurring + +L. blackwoodensis + +and + +L. macedonensis + +, ca. +80 km +further east. The two former species appear to be 'mountain island' endemics, restricted to cloud-stripping forest on higher ground in a landscape which is otherwise largely flat and non-forested. Geographically restricted, forest-dwelling + +Lissodesmus +species + +may be found in future on other isolated mountains in western +Victoria +. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97519C29FF06FE45FC8E03E6.xml b/data/38/2B/5C/382B5C2C97519C29FF06FE45FC8E03E6.xml new file mode 100644 index 00000000000..e2d1387e7f3 --- /dev/null +++ b/data/38/2B/5C/382B5C2C97519C29FF06FE45FC8E03E6.xml @@ -0,0 +1,452 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis yabbra + +n. sp. + + + + + + +Fig. 30 +; map +Fig. 32B + + + + +Holotype + +: Male. +1 male +, +Yabbra State Forest +, NSW, + +2 April 1992 + +, collector unknown. +In +AM +, +KS36844 +. + + + + + +Paratypes + +: In +AM +: +2 males + +, + +Yabbra State Forest +, NSW, + +27 February 1992 + +, +M. Gray +& +D. Charley +, +KS36833 + +. + + + +In +QM +: +2 males +, ' +The Head' +, via +Killarney +, +Qld +, 1974–75, +G. & S. Monteith +, rainforest, +pitfall +22B, +S83693 + +. + + + +FIGURE 30. + +Orthorhachis yabbra + +n. sp. +, male paratype, AM KS36833. (A) medial, (B) lateral and slightly posterior views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + + +Other material examined +: In AM: +1 male +, 1 stadium + +7 female +, +Acacia Plateau and Wilsons Peak +area, +Kooreelah State Forest +, NSW, +28º16'S +152º27'E +, + +11 December 1988 + +, +A.P. Smith +, +H.B. Hines +, +D. Pugh +& P. +Webber +, +pitfall trap +AP7, subtropical rainforest, sheltered slope, +Focal Peak Survey +, +UNE +, +KS39398 + +; + +1 male +, +Goanna Creek +Road, +1.8 km +from junction with +Sandy Creek +Road, +Richmond Range State Forest +, NSW, +28º36'S +152º42'E +, + +4 February–9 April 1993 + +, +M. Gray +& +G. Cassis +, +pitfall +04 +AG +, +KS94870 + +; + +1 male +, same details but +Bennetts Road +, ca. + +10 km +W of Urbenville + +, +Beaury State Forest +, NSW, +28º25'S +152º27'E +, +pitfall +01 +BG +, +KS94879 + +; + +1 male +, same details but +Goanna Creek +Road, +Richmond Range State Forest +, NSW, +28º37'S +152º42'E +, +KS +103054 + +. + + +In + +QM +: +1 male +, +Plateau S +of ' +The Head' +, via +Killarney +, +Qld +, 1974–75, +G. & S. Monteith +, rainforest, +pitfall +21B, +S83692 + +; + +1 male +, same details but +Cunninghams Gap +, +Qld +, +pitfall +31A, +S83694 + +; + +1 male +, +Teviot Falls +via +Boonah +, +Qld +, 1975–76, +G. & S. Monteith +, rainforest, +pitfall +58, +S83695 + +; + +1 male +, +Mt Clunie +via +Woodenbong +, NSW, 1975–76, +G. & S. Monteith +, rainforest, +pitfall +49A, +S83696 + +; + +1 male +, +2 females +, +Lions Road +, Richmond Gap via Grevillea, NSW, 1978–79, +G. Monteith +, rainforest, +pitfall +92, +S83697 + +; + +1 male +, +1 female +, +Atrichornis Track +, +Gibraltar +Range National Park +, NSW, 1980–81, +G. Monteith +, rainforest, +pitfall +105, +S83698 + +. + + +Diagnosis +: Gonopod telopodite bent posterodistally above pronounced constriction at one-third telopodite height; anterior surface with line of evenly spaced teeth; medial process well separated from solenomere base, forked, with lateral branch flexed basally. + + +Description +: As for the genus. Male/female approximate measurements: length 16/ +17 mm +, midbody prozonite diameter 1.4/ +1.5 mm +, midbody width across paranota 2.5/ +2.7 mm +. In alcohol, well-coloured specimens near-uniform medium brown. Antennal sockets separated by 2X a socket diameter. Antennae slender, relative lengths of antennomeres 2>(3,6)>(4,5). Collum D-shaped, as wide as head and narrower than tergite 2. Metatergite sculpture very indistinct, apparently Pattern A. Paranota with anterior margin slightly convex; lateral margin very slightly convex. Legs slender, leg 6 tarsus 1.6X as long as femur. Brush setae with forked tips. + + + +FIGURE 31. +Distribution of + +Orthorhachis catherinae + + +n. sp. + +(open triangles), + +O. cavatica +Jeekel, 2006 + +(star), + +O. christinae + + +n. sp. + +(filled squares) + +O. durabilis + + +n. sp. + +(open circles), + +O. oresbia + + +n. sp. + +(cross), + +O. paradoxalis +Jeekel, 2006 + +(filled triangles), + +O. vinnula + + +n. sp. + +(filled circle) and + +O. tallagandensis + + +n. sp. + +(open square). Mercator projection; scale bar = 200 km. Inset shows location of main map. + + + +Gonopod aperture ovoid, as wide as long, one-third the width of the ring 7 prozonite, rim raised posterolaterally. Telopodite ( +Fig. 30 +) short, base swollen and with long setae on posterolateral surface; telopodite abruptly constricted at about one-quarter telopodite height, more or less cylindrical, curving posteriorly from anterior portion of base, with row of ca. 6 well-spaced, small, rounded teeth along anterior surface from about one-half telopodite height to just above branching point; branching beginning at between two-thirds and three-quarters telopodite height. Solenomere thin, cylindrical, tapering gradually, directed first posterodistally, then curving distally, tip truncate. Medial process not closely applied to solenomere base, very short, divided; medial portion directed posterodistally and with broadly rounded tip, lateral portion finger-like, curving posterobasally with rounded tip. Prostatic groove running laterodistally for short distance on anterior surface of telopodite, then distally, then laterodistally on lateral side of anterior row of teeth to solenomere, and terminating at solenomere tip. + +Female slightly larger than male, legs not swollen. Genital aperture with posterior margin barely raised. Cyphopods not examined. + +Distribution +: Known from ca. +5000 km +2 +across the border between southeastern Queensland and northeastern New South Wales, from Cunninghams Gap south ca. +170 km +to the +Gibraltar +Range ( +Fig. 32B +). Overlaps in range with + +O. monteithi + +and + +O. serrata + +, possibly with + +O. kerewong + +; possibly parapatric with + +O. pallida + +near Cunninghams Gap. + + +Etymology +: Noun in apposition, for the +type +locality, Yabbra State Forest. + + +Remarks +: + +O. yabbra + +varies a little in size across its range. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97559C2CFF06FF7DFC8102F2.xml b/data/38/2B/5C/382B5C2C97559C2CFF06FF7DFC8102F2.xml new file mode 100644 index 00000000000..6f71125835d --- /dev/null +++ b/data/38/2B/5C/382B5C2C97559C2CFF06FF7DFC8102F2.xml @@ -0,0 +1,143 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis tallagandensis + +n. sp. + + + + + + +Fig. 27 +; map +Fig. 31 + + + + +Holotype + +: Male. Approx. + +750 m + +NE of apex of +Mt Bollard +, +Tallaganda State Forest +, NSW, +35º39'14"S +149º28'44"E +, + +1110 m + +(GE), + +15 March 1999 + +, +J. Tarnawski +& +S. Lassau +, +CBCR3-033 +L, leaf litter. +In +AM +, +KS93483 +. + + + +Other material examined +: None available. + + +Diagnosis +: Gonopod telopodite with well and deeply separated branches; medial process terminating in two lobes separated by a wide notch. Posterior sternites with median tab-like structure along posterior edge. + + +Description +: As for the genus. Male approximate measurements: length +14 mm +, midbody prozonite diameter +1.3 mm +, midbody width across paranota +1.8 mm +. In alcohol, body colour near-uniform medium brown. Antennal sockets separated by 2X a socket diameter. Antennae slender, relative lengths of antennomeres 3>(2,6)>(4,5). Collum D-shaped, narrower than head and tergite 2. Metatergite sculpture indistinct, Pattern A. Paranota with anterior margin slightly convex, lateral margin more or less parallel to long axis of body. Legs slender, leg 6 tarsus 1.9X as long as femur. Brush setae with forked tips. Sternites of posterior rings (10–16?) with a small, median, rounded, two-lobed tab on posterior edge, less evident on anterior rings in the tab-bearing set. + + + +FIGURE 27. + +Orthorhachis tallagandensis + + +n. sp. + +, male holotype, AM KS93483. (A) medial, (B) anterior views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + + +Gonopod aperture ovoid, slightly wider than long, one-third the width of the ring 7 prozonite, rim raised posterolaterally. Telopodite ( +Fig. 27 +) short, more or less cylindrical, constricting above broad base and tapering gradually in anterior or posterior view; long setae on posterolateral surface to between one-third and onehalf telopodite height; branching beginning just above one-half telopodite height. Solenomere cylindrical, directed posterodistally, slightly tapering, bending laterally at about three-quarters solenomere height, then curving distally. Medial process well-separated from solenomere, slightly flattened mediolaterally, curving slightly posteriorly, widening near apex and terminating at about three-quarters solenomere height in two lobes separated by a wide notch: anterior lobe distally directed and bluntly rounded, posterior lobe directed posteriorly and slightly distally, with a small, triangular projection on distal surface. + +Female not yet known. + +Distribution +: Known only from at leaf litter at one site in moist montane eucalypt forest in +New South Wales +( +Fig. 31 +). + + +Etymology +: For the +type +locality, Tallaganda State Forest. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97569C2DFF06FD05FE200222.xml b/data/38/2B/5C/382B5C2C97569C2DFF06FD05FE200222.xml new file mode 100644 index 00000000000..bcc1f5e38a1 --- /dev/null +++ b/data/38/2B/5C/382B5C2C97569C2DFF06FD05FE200222.xml @@ -0,0 +1,155 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis vinnula + +n. sp. + + + + + + +Fig. 28 +; map +Fig. 31 + + + + +Holotype + +: +Male. Bennison Plains +, +Vic +, +37º23'13"S +146º43'44"E +, + +1310 m + +(GE), + +21 April 2008 + +, +R +. Mesibov and +T +. Moule, under fallen bark in eucalypt woodland. In +MV +, K-10690. + + + + +Paratypes + +: In + +MV +: +7 males +, details as for +holotype +, K-10691–10697 + +; +7 females +, details as for +holotype +, K- 10698–10704. + + +Other material examined +: None available. + + +Diagnosis +: Gonopod telopodite with solenomere strongly bent posteriorly, tip not reaching as far distally as medial branch. + + +Description +: As for the genus. Male/female approximate measurements: length 19/ +19 mm +, midbody prozonite diameter 1.8/2.0 mm, midbody width across paranota 2.6/ +2.8 mm +. Live animals near-uniform brownish-grey in body colour with reddish legs; the red pigmentation fades quickly in alcohol. Antennal sockets separated by 2X a socket diameter. Antennae slender, relative lengths of antennomeres 3>(2,5)>4>6. Collum D-shaped, as wide as head and narrower than tergite 2. Metatergite sculpture indistinct, Pattern A. Paranota with anterior margin sloping posterolaterally to more or less distinct corner, lateral margin very slightly convex. Legs slender, leg 6 tarsus 1.9X as long as femur. Brush setae with forked tips. + + +Gonopod aperture one-third the width of the ring 7 prozonite, flattened-ovate, wider than long, anterior edge longest and nearly straight, rim raised posterolaterally. Telopodite ( +Fig. 28 +) short, base slightly produced anteriorly and medially, telopodite above base wider mediolaterally than anteroposteriorly, abruptly narrowing medially at just under one-half telopodite height; branching beginning at more than three-quarters telopodite height; long setae on posterolateral surface to about one-third telopodite height. Solenomere directed posteriorly, then abruptly bending distally and slightly laterally and narrowing, then tapering to a point while curving slightly medially. Medial process very closely applied to solenomere base, much wider than solenomere, mediolaterally flattened, directed posterodistally and terminating in two projections separated by a wide, shallow notch: distal projection narrowly triangular, apex pointed, terminating distal to solenomere tip; posterior projection with bluntly rounded tip, extending just posterior to distally directed portion of solenomere and curving slightly laterally. + +Female slightly larger than male, legs not swollen. Genital aperture with posterior margin slightly raised, directed anteroventrally and with a median triangular projection. Cyphopods not examined. + +Distribution +: Known only from the Bennison Plains in the eastern Victorian highlands, north of Licola ( +Fig. 31 +). + + +Etymology +: Latin +vinnulus +, delightful, adjective, for the abundance of specimens at the +type +locality and the ease with which they were collected (see Remarks). + + +Remarks +: Eucalypt woodland on the Bennison Plains was burned in a wildfire in the austral summer of 2006–2007, and recovering trees subsequently shed long strips and sheets of bark. My wife and I found mature males, females and copulating pairs of + +O. vinnula + +under many of these bark pieces, which were lying flat on the ground. We saw no juveniles either on the underside of the bark pieces or on the ground covered by the bark, and it therefore seems likely that the adults were sheltering for the day after wandering at night to disperse or find mates. When disturbed, the animals ran quickly over the bark surface. + +O. vinnula + +was very abundant at the collecting site and at another we visited, several hundred metres distant. We would have collected many more specimens if I had not mistaken this species in the field for the superficially very similar + +Gephyrodesmus arcuatus + +. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97579C2BFF06F975FB900132.xml b/data/38/2B/5C/382B5C2C97579C2BFF06F975FB900132.xml new file mode 100644 index 00000000000..c03c6081ed3 --- /dev/null +++ b/data/38/2B/5C/382B5C2C97579C2BFF06F975FB900132.xml @@ -0,0 +1,197 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis weiri + +n. sp. + + + + + + +Figs. 7C +, +29 +; map +Fig. 32A + + + + +Holotype + +: +Male. Cobark Forest +Park, +Barrington Tops State Forest +, NSW, +31º54'S +151º35'E +, + +15 November 1981 + +, +T +. +Weir +& +A. Calder +, +ANIC +berlesate 754, leaf litter, + +Nothofagus + +rainforest. +In +ANIC +, 64-000191. + + + + + +Paratypes + +: In +ANIC +: +1 male +, +1 female +, details as for +holotype +, 64-000192 + +. + + +Other material examined +: None available. + + +Diagnosis +: Metatergites with Pattern B sculpture. Brush setae with mid-length branch. Gonopod telopodite with apex bent posterodistally, the medial process widely expanded distally and truncate, the poste- rior corner partly enclosing the base of the solenomere. + + +Description +: As for the genus. Male/female approximate measurements: length 10/ +11 mm +, midbody prozonite diameter 0.9/ +1.1 mm +, midbody width across paranota 1.5/ +1.8 mm +. In alcohol, body colour near-uniform light brown. Antennal sockets separated by 2X a socket diameter. Antennae slender, relative lengths of antennomeres 6>3>2>(4,5). Collum D-shaped, narrower than head and tergite 2. Metatergite sculpture very distinct, Pattern B; prozonite with coarse cellular texture, extending to waist across prozonite/metazonite suture ( +Fig. 7C +). Paranota with anterior margin sloping posterolaterally to distinct corner, lateral margin more or less parallel to long axis of body ( +Fig. 7C +). Legs slender, leg 6 tarsus 1.4X as long as femur. Brush setae with mid-length branch as in + +Fig. +1F + +. + + +Gonopod aperture ovoid, slightly wider than long, one-third the width of the ring 7 prozonite, rim raised posterolaterally. Telopodite ( +Fig. 29 +) short, base produced anteriorly, telopodite above base somewhat swollen laterally to about one-third telopodite height and abruptly bending posteriorly at branching point; branching beginning at about two-thirds telopodite height; long setae on posterolateral surface to about one-third telopodite height. Solenomere directed posterodistally, then abruptly bending distally at an 'elbow' and narrowing, then tapering to a point while curving medially. Medial process closely applied to solenomere base, wider than solenomere, directed posterodistally and widening to broad, flat top aligned at about 45º to the telopodite long axis, terminating below the solenomere tip, the posterobasal corner of the top of the medial process curving laterally. + +Female slightly larger than male, legs not swollen. Genital aperture with posterior margin slightly raised in wide, flat-edged flange. Cyphopods not examined. + +Distribution +: Known only from the +type +locality in the Barrington Tops in northern +New South Wales +( +Fig. 32A +); may co-occur with the much larger + +O. inflata + +. + + + +FIGURE 29. + +Orthorhachis weiri + + +n. sp. + +, male paratype, ANIC 64-000192. (A) lateral, (B) posterior, (C) medial views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + + +Etymology +: For CSIRO entomologist Tom Weir, collector of this species and many other new Australian arthropods. + + +Remarks +: The gonopod telopodite of + +O. weiri + +resembles that of + +O. durabilis + +( +Fig. 17 +), and both species have Pattern B metatergite sculpturing ( +Fig. 7 +). The species differ in sculpturing details and in brush setae, which have forked tips in + +O. durabilis + +and a mid-length branch in + +O. weiri + +( +Fig. 1F +). + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97589C23FF06FAADFABD0446.xml b/data/38/2B/5C/382B5C2C97589C23FF06FAADFABD0446.xml new file mode 100644 index 00000000000..84885a8997f --- /dev/null +++ b/data/38/2B/5C/382B5C2C97589C23FF06FAADFABD0446.xml @@ -0,0 +1,342 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis pallida +Jeekel, 1985 + + + + + + + +Figs.1E +, +2C +, +5C +, +6D +, +24 +; map +Fig. 32B + + + + + + + +Orthorhachis pallida +Jeekel, 1985:52 + + +, +Figs. 1–3 +; 2006:73. + + +Shelley +et al +., 2000:118 + + +. + + + + + + +Holotype + +: Male. Bunya Mountains National Park, Koonawarra near Mt Kiangarow, +27 km +WSW of Tarong, Qld, +23 October 1980 +, C.A.W. Jeekel & A.M. Jeekel-Rijvers, along nature track in dry type rainforest, under logs. Possibly in Zoological Museum, Amsterdam; not examined. + + + +Paratypes + +: None. + + +Other material +: In +QM +: + +2 males +, +1 female +, +Ravensbourne National Park +, +Qld +, +Cedar Block Track +, + +26 November 1973 + +, K. +R +. +McDonald +, +S83683 + +; +3 males +, +1 female +, 1 stadium + +7 female +, +Bunya Mountains +, +Qld +, 1974–1975, +G. & S. Monteith +, rainforest +pitfall +19, +S83686 + +; + +1 male +, same details, +S83687 + +; +6 males +, +1 female +, 1 stadium + +7 male +, same details but +Mt Cabinet +via Conondale, +Qld +, +pitfall +29B, +S83684 + +; + +1 male +, same details but +Booloumba Creek +via Conondale, +Qld +, +pitfall +12, +S83685 + +; + +1 male +, +Archookora +via +Nanango +, +Qld +, + +580 m + +, 1975–76, +G. & S. Monteith +, rainforest, +pitfall +62, +S83688 + +; + +1 male +, +Lower Neurum Creek +, +Mt Mee State Forest +, +Qld +, 1977–78, +G. Monteith +, rainforest, +pitfall +90, +S83689 + +; + +3 males +, +4 females +, +Burtons Well +campground, +Bunya Mountains +, +Qld +, + +11 January 1988 + +, +P.M. Johns +, woodpile, +S83690 + +; + +1 male +, +Bare Rock +, + +2 km +N of Mt Cordeaux + +, +Qld +, + +31 December 1993 + +– + +20 February 1994 + +, +G. Monteith +, +pitfalls +, +S83691 + +. + + +Diagnosis +: Gonopod telopodite in lateral or medial view with constriction at about one-third telopodite height, and with apex abruptly bending posteriorly at branching point. + + +Description +: As for the genus; see +Jeekel (1985) +for a detailed description of the + +O. pallida + +holotype +. Male and female approximate measurements: length +18–24 mm +, midbody prozonite diameter +1.6–2.1 mm +, midbody width across paranota +2.4–3.2 mm +. Body slightly discoloured in material examined, light brown. Antennal sockets separated by 2X a socket diameter. Antennae slender, relative lengths of antennomeres 2>(3,6)>(4,5). Collum D-shaped, as wide as head and narrower than tergite 2. Metatergite sculpture indistinct, Pattern A ( +Fig. 6D +). Paranota with anterior margin slightly convex, lateral margin more or less parallel to long axis of body. Legs slender, leg 6 tarsus 1.5X as long as femur ( +Fig. 5C +). Brush setae with forked tips ( +Fig. 1E +). Spinnerets not enclosed by low walls on epiproct ( +Fig. 2C +). + + +Gonopod aperture ovoid, slightly wider than long, about one-third the width of the ring 7 prozonite. Gonopod ( +Fig. 24 +) as described by +Jeekel (1985) +, but all males examined, including those from the +type +locality, also have a small, finger-like projection arising at about two-thirds telopodite height on the lateral side, curving basally and slightly posteriorly. + + +Female not significantly larger than male, legs not swollen. Genital aperture with posterior margin slightly raised in middle in wide inverted +V +, bent slightly anteriorly. Cyphopods not examined. + + +Distribution +: So far known from ca. +8000 km + +2 +in + +far southeastern +Queensland +, from the Bunya Mountains east to the Conondale Range, and south almost to Cunninghams Gap, ca. +25 km +north of the +New South Wales +Border ( +Fig. 32B +). Possibly parapatric with + +O. yabbra + +near Cunninghams Gap. + + +Remarks +: Overall size varies considerably in + +O. pallida + +as circumscribed here. The smallest specimens are from the Bunya Mountains ( +type +locality, and furthest inland) and the largest are from sites closer to the coast. The gonopod telopodite in larger males has a more distinct basally directed lobe on the medial process, and there is less swelling on the lateral side of the telopodite and a sharper concavity on the medial side. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C975A9C21FF06FF7DFCBF036A.xml b/data/38/2B/5C/382B5C2C975A9C21FF06FF7DFCBF036A.xml new file mode 100644 index 00000000000..cc7832782b4 --- /dev/null +++ b/data/38/2B/5C/382B5C2C975A9C21FF06FF7DFCBF036A.xml @@ -0,0 +1,221 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis paradoxalis +Jeekel, 2006 + + + + + + + +Figs. 4A, 4B +, +25 +; map +Fig. 31 + + + + + +Orthorhachis paradoxalis +Jeekel, 2006:74 + +, +Figs. 1–3 +. + + + + + +Holotype + +: Male. Paradox Cave J48, Jenolan, NSW, +2 January 1973 +, E. Hamilton-Smith, field code BS2183. Not examined. + + + +Paratypes + +: None. + + +Other material +: In +AM +: +1 male +, 2 stadium + +7 females +, +Grill Cave +, +Bungonia +, NSW, + +20 April 1971 + +, +G. Wellings +, +KS94904 + +; + +5 males +, +3 females +, +Budthingeroo Creek +, +Boyd Plateau +via +Jenolan Caves +, NSW, near pluviometer, + +3500 ft + +, + +9 September 1972 + +, +G.S. Hunt +, under logs, +KS94893 + +; + +3 males +, +1 female +, +Jenolan Caves area +, NSW, southern limestone area, + +6 July 1989 + +, +G.S. Hunt +, +KS21677 + +; + +1 male +, +5 females +, same details but + +14 August 1989 + +, +KS22527 + +. + + +Diagnosis +: Gonopod telopodite with tight medial loop in solenomere. Posterior sternites with median tablike structure along posterior edge. + + + +FIGURE 25. + +Orthorhachis paradoxalis +Jeekel, 2006 + +, male, AM KS94893. (A) anterior, (B) lateral, (C) posterior views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + + +Description +: As for the genus; see Jeekel (2006) for a detailed description of the + +O. paradoxalis + +holotype +. Male/female approximate measurements: length 18/ +19 mm +, midbody prozonite diameter 1.4/ +1.5 mm +, mid- body width across paranota 2.1/ +2.2 mm +. Body slightly discoloured, light brown. Antennal sockets separated by 2X a socket diameter. Antennae slender, relative lengths of antennomeres (2,3)>6>(4,5). Collum D-shaped, as wide as head and and tergite 2. Metatergite sculpture indistinct, Pattern A. Paranota with anterior margin slightly convex, lateral margin very slightly convex. Legs slender, leg 6 tarsus 1.5X as long as femur. Brush setae with forked tips. Sternites of posterior rings (10–18?) with a small, median, rounded, two-lobed tab on posterior edge ( +Figs. 4A, 4B +), less evident on anterior rings in the tab-bearing set. + + +Gonopod aperture ovoid, slightly wider than long, one-third the width of the ring 7 prozonite, rim raised posterolaterally. Gonopod telopodite ( +Fig. 25 +) as described by Jeekel (2006). + +Female slightly larger than male, legs slender and not swollen, no sternite tabs. Genital aperture with posterior margin raised in wide, almost flat-topped flange, bent slightly anteriorly at corners. Cyphopods not examined. + +Distribution +: Known from a cluster of three closely adjacent sites in southeastern +New South Wales +near Jenolan, and a cave site ca. +110 km +to the south ( +Fig. 31 +). The fact that the Budthingeroo Creek collection was not in a cave indicates that + +O. paradoxalis + +, like a number of other Australian dalodesmids, is only an accidental cave inhabitant. + + +Remarks +: See comment on +types +for + +O. cavatica + +, above. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C975B9C2EFF06FC8DFBCE0792.xml b/data/38/2B/5C/382B5C2C975B9C2EFF06FC8DFBCE0792.xml new file mode 100644 index 00000000000..e01ddac3f85 --- /dev/null +++ b/data/38/2B/5C/382B5C2C975B9C2EFF06FC8DFBCE0792.xml @@ -0,0 +1,353 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis serrata + +n. sp. + + + + + + +Fig. 26 +; map +Fig. 32A + + + + +Holotype + +: +Male. Creek +Road, +Beaury State Forest +, NSW, +28º24'S +152º27'E +, + +4 February–9 April 1993 + +, +M. Gray +& +G. Cassis +, +pitfall trap +. +In +AM +, +KS +103053. + + + + + +Paratypes + +: In +AM +: +2 males +, +1 female + +, + +details as for +holotype +, +KS93759 +; +1 male +, +1 female + +, + +same details but +Tucker Box Road +, +Beaury State Forest +, NSW, +28º28'S +152º24'E +, +KS93751 + +. + + + +Other material examined +: +In +AM +: +1 male + +, + +Tweed Range +, NSW, +28º28'S +153º08'E +, + +1000–1200 m + +, + +17 February 1989 + +, +A.P. Smith +, +H.B. Hines +, D. +Pugh +& P. +Webber +, +Mt Warning Caldera Survey +, cool temperate rainforest, +pitfall trap +T2.14 +, +KS50114 +; +1 male + +, + +details as for +holotype +but +Stockyard Fire Trail +, +Chaelundi State Forest +, NSW, +29º57'S +152º31'E +, +KS93753 +; +1 male + +, + +same details but +Mt Tindal Road +, +Ramornie State Forest +, NSW, +29º42'S +152º35'E +, 20 +CM +, +KS94871 +; +1 male + +, + +same details but +Opposum Creek +upstream of +Foamy Creek +Road, +Marengo State Forest +, NSW, +30º06'S +152º25'E +, +KS94880 +; +1 male + +, + +same details but ca. + +600 m + +down small track off +Dorrigo-Bellingen +highway, < + +1 km +W of Summervilles Road + +, NSW, +30º25'S +152º45'E +, 31 +CG +, +KS94883 +; +1 male + +, + +same details but + +100 m + +SW of junction of +Hallgraths Trail +and +Sherwood Road +, +Conglomerate State Forest +, NSW, +30º06'S +153º03'E +, 22AR, +KS94887 +; +1 male + +, + +same details but headwaters of +Valorem Creek +, track off +Mt Tindal Road +, +Ramornie State Forest +, NSW, +29º42'S +152º35'E +, 20 +CG +, +KS94890 + +. + + +Diagnosis +: Gonopod telopodite with toothed crest on anterior surface from one-half telopodite height to branching point, and with medial process broadly rounded distally, not extending posterolaterally. + + +Description +: As for the genus. Male/female approximate measurements: midbody prozonite diameter 1.2/ +1.5 mm +, midbody width across paranota 2.0/ +2.4 mm +. In alcohol, well-coloured specimens near-uniform chestnut brown. Antennal sockets separated by 2X a socket diameter. Antennae slender, relative lengths of antennomeres 3>(2,6)>(4,5). Collum D-shaped with posterior margin slightly emarginate on either side, as wide as head and narrower than tergite 2. Metatergite sculpture indistinct, Pattern A. Paranota with anterior margin slightly convex, hardly roughened; lateral margin very slightly convex. Legs slender, leg 6 tarsus 1.4X as long as femur. Brush setae with forked tips. + + +Gonopod aperture ovoid, slightly wider than long, one-third the width of the ring 7 prozonite, rim raised posterolaterally. Telopodite ( +Fig. 26 +) short, more or less cylindrical, constricting above broad base and tapering gradually, distally curving slightly posteriorly; long setae on posterolateral surface to between one-third and one-half telopodite height; branching beginning above three-quarters telopodite height. Solenomere cylindrical, directed posterodistally, slightly tapering. Medial process closely applied to solenomere base, broadly rounded, flattened mediolaterally, terminating at about one-half solenomere height, with a small, bluntly rounded tooth on posterior edge. Telopodite with a similar tooth on posterior surface of telopodite at or just below branching point. On anterior surface of telopodite, a row of ca. 10 teeth with anterobasally curving tips, diminishing in size from telopodite branching point to ca. one-half telopodite height. Prostatic groove running laterodistally for short distance on anterior surface of telopodite, then distally to solenomere, running just lateral to row of teeth on anterior surface of telopodite, and terminating at solenomere tip. + +Female larger than male, legs slender and not swollen. Genital aperture with posterior margin slightly raised in very slightly convex flange, bent slightly anteriorly at corners. Cyphopods not examined. + +Distribution +: Known from ca. +20000 km + +2 +in + +far northeastern +New South Wales +, from just south of the +Queensland +border to just south of Dorrigo ( +Fig. 32A +). Overlaps in range with + +O. yabbra + +; possibly parapatric with + +O. jubata + +, + +O. kerewong + +and + +O. weiri + +. + + +Etymology +: Latin +serratus +, saw-toothed, adjective, for the line of teeth on the anterior surface of the gonopod telopodite. + + +Remarks +: Male and female lengths could not be estimated, as all specimens examined are from pitfall traps and much 'loosened' by partial maceration. + + + +FIGURE 26. + +Orthorhachis serrata + + +n. sp. + +, male paratype, AM KS93759. (A) lateral, (B) anterior, (C) medial views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + + +The Tweed Range male is assigned to this species only tentatively. It is considerably larger than other + +O. serrata + +and the posterior corners of the paranota are more extended. The gonopod telopodite in this specimen agrees in details with that of the +types +but is more strongly curved posteriorly. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C975C9C27FF06FE6DFDD70132.xml b/data/38/2B/5C/382B5C2C975C9C27FF06FE6DFDD70132.xml new file mode 100644 index 00000000000..366d9dbf12b --- /dev/null +++ b/data/38/2B/5C/382B5C2C975C9C27FF06FE6DFDD70132.xml @@ -0,0 +1,256 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis kerewong + +n. sp. + + + + + + +Figs. 1F +, +4C +, +5E +, +7B +, +21 +; map +Fig. 32A + + + + +Holotype + +: +Male. Kerewong State Forest +, NSW, +31º36'S +152º34'E +, + +20 November 1978 + +, +D. Milledge. In +AM +, +KS94911 +. + + + + + +Paratypes + +: In +AM +: +2 males +, +1 female + +, + +details as for +holotype +but + +November 1978 + +, +KS94910 +; +1 male + +, + +Middle Brother State Forest +, NSW, + +15 December 1978 + +, +D. Milledge +, field no. 1556, +pitfall trap +, +KS16112 + +. + + + +In +QM +: +1 male +, +Bruxner Park +, + +5 km +N of Coffs Harbour + +, NSW, +30º15'00"S +153º06'10"E +, + +150 m + +, 1980–81, +G. Monteith +, rainforest +pitfall +104/B1, +S83676 + +; + +2 males +, 1 stadium +7 male +, 1 stadium +6 male +, +Poverty Point +, +SE of Tenterfield +, NSW, + +1160 m + +, 1978–79, +G. Monteith +, rainforest +pitfall +94, +S83677 + +. + + +Other material examined +: + +In +QM +: +1 male +, +Point Lookout +(upper), +New +England +National Park +, NSW, + +11 March –11 November 1980 + +, +G. Monteith +, +pitfall +, +S83678 + +. + + +Diagnosis +: Metatergites with Pattern B sculpture. Brush setae with mid-length branch. Gonopod telopodite with two processes arising from approximately the same point on the anteromedial surface, the processes 'crossing' with the larger directed laterodistally, the smaller laterobasally. + + +Description +: As for the genus. Male/female approximate measurements: length 18/ +18 mm +, midbody prozonite diameter 1.7/ +1.7 mm +, midbody width across paranota 2.7/ +2.6 mm +. In alcohol, well-coloured specimens dark brown with pale paranotal margins. Antennal sockets separated by 2X a socket diameter. Antennae slen- der, relative lengths of antennomeres 6>(2,3)>(4,5). Collum broadly fusiform with projecting corners, as wide as head and narrower than tergite 2. Metatergite sculpture distinct, Pattern B ( +Fig. 7B +). Paranota with anterior margin sloping posterolaterally to distinct corner, lateral margin more or less parallel to long axis of body ( +Fig. 7B +). Legs slender, leg 6 tarsus 2X as long as femur ( +Fig. 5E +). Brush setae with mid-length branch ( +Fig. 1F +). Spinnerets partly enclosed by low walls on epiproct ( +Fig. 4C +). + + +Gonopod aperture ovoid, slightly wider than long, about one-third the width of the ring 7 prozonite, rim raised posterolaterally. Telopodite ( +Fig. 21 +) short, slender, roughly cylindrical and upright; long setae on posterolateral surface to about one-third telopodite height; branching beginning at three-quarters telopodite height; posterolateral surface of telopodite broadly excavated to base. Solenomere a tapering cylinder, directed posterodistally and slightly medially, then curving distally, the tip bending posteromedially. Medial process small, close to solenomere at base and reaching distally to about one-third solenomere height, bending medially and curving posteriorly, terminating in a broadly rounded tip. Two additional processes arising close together on anteromedial surface of telopodite at just over one-half telopodite height: medial process a tapering cylinder directed laterodistally across anterior surface of telopodite and terminating at same level as medial branch of telopodite; lateral process about one-third the length of the adjacent medial process, more or less triangular, directed laterobasally. Prostatic groove running laterodistally for short distance, then abruptly distally, passing lateral to paired processes to solenomere, terminating at solenomere tip. + +Female not significantly larger than male, legs slender and not swollen. Genital aperture with posterior margin raised in wide, more or less flat-topped flange, bent slightly anteriorly at corners. Cyphopods not examined. + +Distribution +: Disjunct localities in northeastern +New South Wales +over a linear range of ca. +300 km +( +Fig. 32A +). + + +Etymology +: Noun in apposition, for the +type +locality, Kerewong State Forest. The place name 'Kerewong' probably refers to an Australian Aboriginal word, but the spelling 'kerewong' is not recorded in any +New South Wales +Aboriginal word lists (C. Jarvis pers. comm., A. Lissarrague, pers. comm.). Similar Aboriginal words adopted into English are 'currawong', for one of several cracticine artamid birds, and 'currawang', for the wattle tree + +Acacia doratoxylon + +. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C975D9C25FF06F99FFB85014A.xml b/data/38/2B/5C/382B5C2C975D9C25FF06F99FFB85014A.xml new file mode 100644 index 00000000000..aab20786622 --- /dev/null +++ b/data/38/2B/5C/382B5C2C975D9C25FF06F99FFB85014A.xml @@ -0,0 +1,213 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis monteithi + +n. sp. + + + + + + +Fig. 22 +; map +Fig. 32B + + + + +Holotype + +: Male. +Mt Superbus +, +Qld +, summit, + +1300 m + +, + +8–9 February 1990 + +, +G. Monteith +, +G. Thompson +and +H. Janetzki. In +QM +, +S83679 +. + + + + + +Paratypes + +: +In +QM + +: +1 male +, 1 stadium + +7 female +, +Mt Asplenium +, +Qld +, + +18–20 December 1992 + +, +G. Monteith +, +S83680 + +; +1 male +, 1 stadium + +7 female +, +Mt Asplenium +, +Qld +, + +29–30 January 1993 + +, +G. Monteith +, +S83681 + +; + +1 male +, +Mt Superbus +, +Qld +, summit, + +1350 m + +, + +24 October 1998 + +, +G. Monteith +, +QM +berlesate 973, rainforest, stick brushings, +S83682 + +. + + +Other material examined +: None available. + + +Diagnosis +: Gonopod telopodite with flat, wing-like process on the anteromedial surface, the process rounded posterodistally and toothed on the anterior edge. + + +Description +: As for the genus. Male approximate measurements: length +19 mm +, midbody prozonite diameter +1.6 mm +, midbody width across paranota +2.9 mm +. Body discoloured, near-uniform light brown. Antennal sockets separated by 2X a socket diameter. Antennae slender, relative lengths of antennomeres 3>(2,6)>(4,5). Collum D-shaped, as wide as head and narrower than tergite 2. Metatergite sculpture fairly distinct, Pattern A. Paranota with anterior margin convex, lateral margin very slightly convex. Legs slender, leg 6 tarsus 1.5X as long as femur. Brush setae with forked tips. + + +Gonopod aperture ovoid, slightly wider than long, about one-third the width of the ring 7 prozonite, rim raised posterolaterally. Telopodite ( +Fig. 22 +) short, a slightly tapering cylinder above a broad base, distally curving slightly posteriorly; long setae on posterolateral surface to between one-third and one-half telopodite height; branching beginning at three-quarters telopodite height. Solenomere a tapering cylinder, somewhat flattened anteroposteriorly, directed posterodistally and curving slightly laterally. Medial process closely pressed to solenomere at base and angled to lie posteromedial to solenomere; process broad, somewhat flattened mediolaterally, with a wide, slightly convex distal edge reaching to one-half solenomere height; with a small, tooth-like projection on posterior edge and a short, truncate projection on distal edge opposite (and supporting?) solenomere. Telopodite also with a short, bluntly rounded projection on posterior surface of telopodite just below branching point, and a large wing-like process on anteromedial surface of telopodite from about half telopodite height to just below branching point, the latter strongly flattened mediolaterally, rounded on posterior and distal edges and irregularly toothed on anterior edge. Prostatic groove running laterodistally for short distance on anterior surface of telopodite, then distally to base of wing-like process, then laterodistally and slightly posteriorly along solenomere to tip. + +Adult female not yet recognised. + + +FIGURE 22. + +Orthorhachis monteithi + + +n. sp. + +, male paratype, QM +S83681 +. (A) lateral, (B) anterior, (C) medial views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + + +Distribution +: So far known only from two mountains ca. +10 km +apart in Main Range National Park in far southeastern +Queensland +( +Fig. 32B +). Overlaps in range with + +O. yabbra + +. + + +Etymology +: For Geoff Monteith, the former Curator of Insects at the +Queensland +Museum, whose diligent collecting has greatly increased our knowledge of the +Queensland +arthropod fauna. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C975F9C22FF06FE68FF0D048A.xml b/data/38/2B/5C/382B5C2C975F9C22FF06FE68FF0D048A.xml new file mode 100644 index 00000000000..adf1bc5f779 --- /dev/null +++ b/data/38/2B/5C/382B5C2C975F9C22FF06FE68FF0D048A.xml @@ -0,0 +1,178 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis oresbia + +n. sp. + + + + + + +Fig. 23 +; map +Fig. 31 + + + + +Holotype + +: Male. The Big Culvert, + +2.5 km +ENE of Mt Observation + +, +Vic +, +37º33'36"S +145º52'15"E +, + +26 October – 28 December 1995 + +, +G. Milledge +, +pitfall traps +, + +Nothofagus cunninghamii + +forest. +In +MV +, K-10689. + + + + +FIGURE 23. + +Orthorhachis oresbia + + +n. sp. + +, male paratype, WAM T76319. (A) medial, (B) anterior views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + + + + +Paratype + +: In +WAM +: +1 male + +, + +Cumberland Falls +, +Vic +, +37º34'S +145º53'E +, + +27 May 1991 + +, +M.S. Harvey +& +M.E. Blosfelds +, +T +76139 + +. + + +Other material examined +: None available. + + +Diagnosis +: Gonopod telopodite curving anteriorly above pronounced mid-length constriction; medial process small, forked, the two tips enclosing the solenomere base. + + +Description +: As for the genus. Male approximate measurements: length +17 mm +, midbody prozonite diameter +1.5 mm +, midbody width across paranota +2.3 mm +. Body slightly discoloured, light brown ( +paratype +). Antennal sockets separated by 2X a socket diameter. Antennae slender, relative lengths of antennomeres (2,3)>6>(4,5). Collum D-shaped, as wide as head and narrower than tergite 2. Metatergite sculpture very distinct, Pattern A. Paranota with anterior margin distinctly roughened, almost serrate, sloping to join lateral margin in gentle curve, lateral margin more or less straight and slightly flared outwards posteriorly, marginal notches very distinct. Legs slender, leg 6 tarsus 1.5X as long as femur. Brush setae with forked tips. + + +Gonopod aperture ovoid, slightly wider than long, about one-third the width of the ring 7 prozonite, rim raised posterolaterally. Telopodite ( +Fig. 23 +) short, base strongly produced basally on medial side; long setae on posterolateral surface to one-third telopodite height; branching beginning above three-quarters telopodite height. Above broad base, telopodite more or less cylindrical to one-half telopodite height, then abruptly tapering and nearly C-shaped in lateral view (concave posteriorly). Solenomere cylindrical, very short, directed posterodistally, curving slightly medially, the tip mediolaterally flattened. Medial process closely applied to solenomere base, forked at base, with bluntly rounded posterior branch paralleling and adjoining solenomere and terminating at about one-half solenomere height, and with short, bluntly pointed anterior branch directed laterally, curving slightly basally and lying anterior to solenomere base. Prostatic groove running laterodistally for short distance on anterior surface of telopodite, then distally to abrupt taper in telopodite, then laterodistally and slightly anteriorly to solenomere, and terminating at solenomere tip. + +Female not yet recognised. + +Distribution +: Known only from two sites in eastern +Victoria +less than +5 km +apart ( +Fig. 31 +). Possibly sympatric with + +O. durabilis + +. + + +Etymology +: Greek +oresbios +, mountain-living, adjective, referring to the mountains where this species occurs. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97609C1BFF06FF7DFB0A0192.xml b/data/38/2B/5C/382B5C2C97609C1BFF06FF7DFB0A0192.xml new file mode 100644 index 00000000000..acfdefd93d9 --- /dev/null +++ b/data/38/2B/5C/382B5C2C97609C1BFF06FF7DFB0A0192.xml @@ -0,0 +1,149 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis gloriosa + +n. sp. + + + + + + +Fig. 18 +; map +Fig. 32B + + + + +Holotype + +: Male. +Mt Glorious +, Qld, Hiller property, 1977–78, +G. Monteith +, rainforest +pitfall +91. In +QM +, +S83671 +. + + + + + +Paratypes + +: In +QM +: +2 males + +, + +details as for +holotype +, +QM +S83672 + +. + + +Other material examined +: None available. + + +Diagnosis +: Gonopod telopodite with dentate flange extending basally from base of solenomere on posterolateral surface. + + +Description +: As for the genus. Male approximate measurements: length +14 mm +, midbody prozonite diameter +1.1 mm +, midbody width across paranota +1.8 mm +. Body discoloured, near-uniform light brown. Antennal sockets separated by 2X a socket diameter. Antennae slender, relative lengths of antennomeres (2,3,6)>(4,5). Collum D-shaped, posterior margin slightly emarginate on either side, as wide as head and narrower than tergite 2. Metatergite sculpture distinct, Pattern A. Paranota with anterior margin sloping posterolaterally to distinct corner, lateral margin parallel to long axis of body. Legs slender, leg 6 tarsus 1.6X as long as femur. Brush setae with forked tips. + + + +FIGURE 18. + +Orthorhachis gloriosa + +n. sp. +, male paratype, QM +S83672 +. (A) lateral, (B) anterior, (C) medial, (D) posterior views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + + +Gonopod aperture ovoid, wider than long, slightly wider anteriorly, one-third the width of the ring 7 prozonite, rim raised posterolaterally. Telopodite ( +Fig. 18 +) short, base broad and swollen posterolaterally to about half telopodite height; long setae on posterolateral surface to between one-third and one-half telopodite height; branching beginning at three-quarters telopodite height. Solenomere rod-like, slightly tapered, directed distally and slightly posteriorly with bluntly rounded tip; posterolateral surface extended basally as posterolaterally directed flange, nearly as long as solenomere, with ca. 7 widely spaced marginal teeth. Medial process standing very close to solenomere, expanding distally and flattening mediolaterally, terminating at about half solenomere height with broad, slightly convex edge facing distally and slightly posteriorly, the posterior corner projecting posteriorly about as far as solenomere in lateral view. + +Female not yet recognised. + +Distribution +: Known only from the +type +locality, ca. +30 km +northwest of Brisbane in southeastern +Queensland +( +Fig. 32B +). + + +Etymology +: Latin +gloriosus +, splendid, adjective, referring to Mt Glorious, the +type +locality. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97619C18FF06FDA5FF310514.xml b/data/38/2B/5C/382B5C2C97619C18FF06FDA5FF310514.xml new file mode 100644 index 00000000000..8e0ca009258 --- /dev/null +++ b/data/38/2B/5C/382B5C2C97619C18FF06FDA5FF310514.xml @@ -0,0 +1,215 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis inflata + +n. sp. + + + + + + +Fig. 19 +; map +Fig. 32A + + + + +Holotype + +: +Male. Wilson River Reserve +via +Bellangty +, NSW, +31º12'S +152º28'E +, + +November 1966 + +, +D.K. McAlpine. In +AM +, +KS94159 +. + + + + + +Paratypes + +: +In +AM +: +1 male + +, + +details as for +holotype +, +KS94152 +; +1 male + +, + +details as for +holotype +, +KS94160 +; +1 male +, +1 female + +, + +Fifes Knob Road +, ca. +3 km +from +Fifes Fire Trail +, +Carrai State Forest +, NSW, +30º54'S +152º22'E +, + +4 February – 9 April 1993 + +, +M. Gray +and +G. Cassis +, 38 +CM +, +KS94877 + +. + + + +In +MV +: +1 male +, +Barrington Tops +, NSW, + +January 1926 + +, +C. Barrett +, K-10688 + +. + + +Other material examined +: None available. + + +Diagnosis +: Gonopod telopodite with large anterior swelling, with solenomere extending anteriorly above a distinct 'elbow', and with medial process lying posterior to solenomere, terminating in three large lobes and with a dentate lateral margin. + + +Description +: As for the genus. Male/female approximate measurements (see below, Remarks): length 19/ +18 mm +, midbody prozonite diameter 1.4–1.6/ +1.7 mm +, midbody width across paranota 2.1–2.5/ +2.4 mm +. Body discoloured, near-uniform light brown. Antennal sockets separated by 2X a socket diameter. Antennae slen- der, relative lengths of antennomeres 3>(2,6)>(4,5). Collum D-shaped, posterior margin slightly emarginate on either side, as wide as head and narrower than tergite 2. Metatergite sculpture fairly distinct, Pattern A. Paranota with anterior margin convex, lateral margin more or less parallel to long axis of body. Legs slender, leg 6 tarsus 1.5X as long as femur. Brush setae with forked tips. + + +Gonopod aperture ovoid, slightly wider than long, one-half the width of the ring 7 prozonite, rim raised posterolaterally. Telopodite ( +Fig. 19 +) short, broad at base; long setae on posterolateral surface to one-third telopodite height; branching beginning at between one-half and two-thirds telopodite height. Telopodite basally with a large, rounded anterior swelling from about one-quarter to about one-half telopodite height, and with a small, thin flange with a few marginal teeth on medial surface at the same level as swelling. Solenomere arising anteriorly and slightly laterally, curving slightly laterally, then turning abruptly anteromedially at a distinct 'elbow', then tapering and curving tightly posteriorly at the tip in a plane at right angles to telopodite axis. Medial process arising posteriorly and slightly medially, broad than solenomere at base, anteroposteriorly flattened with lateral margin toothed, expanding distally and terminating just below level of solenomere 'elbow', the distal margin divided into three lobes: a broad lateral projection with a laterobasally directed, bluntly rounded tip; a small, truncate central projection; and a small, bluntly pointed medial projection, with a deep cleft between central and medial projections. Prostatic groove running laterodistally for short distance on anterior surface of telopodite, then distally, then abruptly laterodistally above anterior swelling of telopodite, and following curves of solenomere to tip. + +Female with legs not swollen. Posterior margin of genital aperture slightly raised in low, convex arc. Cyphopods not examined. + + +FIGURE 19. + +Orthorhachis inflata + + +n. sp. + +, male paratype, AM KS94160. (A) lateral, (B) anterior, (C) medial, (D) posterior views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + + +Distribution +: Known from three sites in northeastern +New South Wales +over a linear range of ca. +150 km +( +Fig. 32A +). May co-occur with the much smaller + +O. weiri + +in the Barrington Tops. + + +Etymology +: Latin +inflatus +, swollen, adjective, for the large swelling on the anterior surface of the gonopod telopodite. + + +Remarks +: Body sizes given in the description are for partly macerated specimens and are highly approximate. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97629C26FF06FA38FDFB014A.xml b/data/38/2B/5C/382B5C2C97629C26FF06FA38FDFB014A.xml new file mode 100644 index 00000000000..fb1c5eccfde --- /dev/null +++ b/data/38/2B/5C/382B5C2C97629C26FF06FA38FDFB014A.xml @@ -0,0 +1,183 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis jubata + +n. sp. + + + + + + +Fig. 20 +; map +Fig. 32B + + + + +Holotype + +: +Male. Palm Grove +, +Tamborine +, +Qld, G. +& S. Monteith [possibly 1972], +pitfall +37 +A. In +QM +, +S83673 +(in two pieces, anterior end in genitalia vial). + + + + + +Paratypes + +: In +QM +: +1 male +, +Mt Tamborine +, +Qld +, 1979, +J. Grimshaw +, rainforest, +pit traps +, +S83674 + +; + +1 male +, +1 female +, +Numinbah Arch +, +Qld +, +28º14'S +153º14'E +, + +1 January–29 February 1992 + +, +D.J. Cook +, rainforest, +pitfall +, +S83675 + +. + + +Other material examined +: None available. + + +Diagnosis +: Gonopod telopodite with short, posterolaterally directed medial process, and with a toothed crest anterior to the medial process continuing as a line of evenly spaced teeth on the anterior surface of the telopodite. + + +Description +: As for the genus. Male and female approximate measurements: length +16 mm +, midbody prozonite diameter +1.5 mm +, midbody width across paranota +2.2 mm +. Body discoloured, near-uniform light brown. Antennal sockets separated by 2X a socket diameter. Antennae slender, relative lengths of antennomeres 2>6>3>(4,5). Collum D-shaped, as wide as head and narrower than tergite 2. Metatergite sculpture indistinct, Pattern A. Paranota with anterior margin convex and not noticeably roughened, lateral margin very slightly convex. Legs slender, leg 6 tarsus 1.6X as long as femur. Brush setae with forked tips. + + +Gonopod aperture longer than wide, wider anteriorly, about one-third the width of the ring 7 prozonite, rim raised posterolaterally. Telopodite ( +Fig. 20 +) short, broad at base below abrupt constriction, slightly tapering distal to constriction and bending slightly posteriorly; long setae on posterolateral surface to between onethird and one-half telopodite height; branching beginning at three-quarters telopodite height. From about onequarter telopodite height, telopodite with a line of evenly spaced, rounded teeth on anteromedial surface, continued as an irregular toothed crest on anterodistal portion of base of medial process. Solenomere a tapering cylinder, directed distally and slightly posterolaterally and curving slightly distally. Medial process well-separated from solenomere, small, triangular, directed posterolaterally and lying posterior to solenomere base. Prostatic groove running laterodistally for short distance on anterior surface of telopodite, then distally lateral to line of teeth, then tightly looping posterodistally at base of medial process, then following curve of solenomere to tip. + + + +FIGURE 20. + +Orthorhachis jubata + + +n. sp. + +, male paratype, QM +S83675 +. (A) anterior, (B) medial, (C) posterior views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + +Female not significantly larger than male, legs very slender and not swollen. Genital aperture with posterior margin raised in wide, almost flat-topped flange, bent slightly anteriorly, with small median tooth. Cyphopods not examined. + +Distribution +: Known from three sites in far southeastern +Queensland +over a linear range of ca. +35 km +( +Fig. 32B +). Possibly parapatric with + +O. serrata + +and + +O. yabbra + +. + + +Etymology +: Latin +jubatus +, crested, adjective. In side view the gonopod telopodite resembles a lizard with a toothed crest on head and back. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97649C1FFF06FF7DFB4C057D.xml b/data/38/2B/5C/382B5C2C97649C1FFF06FF7DFB4C057D.xml new file mode 100644 index 00000000000..b405f8e1c81 --- /dev/null +++ b/data/38/2B/5C/382B5C2C97649C1FFF06FF7DFB4C057D.xml @@ -0,0 +1,371 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis christinae + +n. sp. + + + + + + +Fig. 16 +; map +Fig. 31 + + + + +Holotype + +: Male. +Mt Wilson +, NSW, +33º30'S +150º23'E +, + +26 January 1979 + +, +C. Horseman. In +AM +, +KS94913 +. + + + + + +Paratypes + +: +In +AM +: +2 males +, +1 female + +, + +details as for +holotype +, +KS94912 +; +1 male + +, + +details as for +holotype +, +KS +103049 (ex +KS94913 +) + +; +1 male +, + +same details but +Cathedral of Ferns +area, + +29 November 1978 + +, field no. 1215, +KS +103047; +3 males +, +1 female + +, + +same details but +Waterfall Picnic Area +Trail, + +29 November 1979 + +, field no. 1624, +KS +103050 + +. + + +Other material examined +: In AM: + +1 male +, +1 female +, +Mt Keira Fauna Reserve Scout Camp +, NSW, +34º24'S +150º51'E +, + +6 December 1978 + +, +C. Horseman +, field no. 1217, +KS +103048 + +; +2 males +, 1 stadium + +7 male +, same details but + +25 April 1979 + +, field no. 1564, +KS18491 + +; + +1 male +, +Binnowee Drive +, +Blue Mountains National Park +, NSW, +33º40'15"S +150º27'55"E +, + +580 m + +(GE), + +15 August 1996 + +, +Australian Museum Business Services +, +pitfall traps +, site K42 CU2, +KS53430 + +; + +1 male +, +1 female +, +Coates Park +, +Hazelbrook +, NSW, +33º43'45"S +150º26'45"E +, + +640 m + +(GE), + +22 August 1996 + +, +Australian Museum Business Services +, +pitfall traps +, site M9 AU3, +KS66150 + +; + +1 male +, +1 female +, +Ridge Street +, +Woodford +, NSW, +33º43'50"S +150º28'40"E +, + +600 m + +(GE), + +30 September 1996 + +, +Australian Museum Business Services +, +pitfall traps +, site M1 BU2, +KS53429 + +; + +1 male +, +2 females +, +Railway Parade +, +Hazelbrook +, NSW, +33º43'55"S +150º27'00"E +, + +620 m + +(GE), + +3 October 1996 + +, +Australian Museum Business Services +, +pitfall traps +, site M4 AU4, +KS66149 + +. + + + +In +ANIC +: +1 male +, +Mt Keira Scout Camp +, NSW, +34º24'S +150º50'E +, + +320 m + +, + +5 March 1981 + +, +J. Lawrence +& +A. Calder +, +ANIC +berlesate 709, leaf litter under palms, 64-000186 + +. + + +Diagnosis +: Gonopod telopodite with solenomere and medial process close together at bases, the medial process terminating in three lobes, the most distal being the central one. + + +Description +: As for the genus. Male/female approximate measurements, Mt Wilson, Mt Keira: length 16/ 17, 25/ +26 mm +; midbody prozonite diameter 1.5/1.7, 2.0/ +2.2 mm +; midbody width across paranota 2.1/2.2, 3.0/ +3.2 mm +. Well-coloured specimens in alcohol chestnut brown with lighter paranotal corners. Antennal sockets separated by just over 2X a socket diameter. Antennae slender, relative lengths of antennomeres (2,3)>6>(4,5) in smaller specimens, 3>(2,5)>6> +4 in +Mt Keira specimens. Collum D-shaped with sharp corners, about as wide as head and narrower than tergite 2. Metatergite sculpture variably distinct, Pattern A. Paranota with anterior margin convex, curving smoothly to join lateral margin without distinct corner; lateral margin parallel to long axis of body. Legs slender, leg 6 tarsus 1.7–1.8X as long as femur. Brush setae with forked tips. + + +Gonopod aperture ovoid but wider anteriorly, slightly wider than long, about one-third the width of the ring 7 prozonite, rim raised posterolaterally. Telopodite ( +Fig. 16 +) short, base broad and wider than long; telopodite flattening mediolaterally distad; long setae on posterolateral surface to one-quarter telopodite height; branching beginning at between one-half and two-thirds telopodite height. Solenomere a gradually tapering cylinder with a truncated tip, curving posteriorly, then abruptly turning distally and very slightly laterally at an 'elbow'. Medial process closely pressed to solenomere at base, flattened mediolaterally, curving posteriorly and terminating just above level of solenomere 'elbow' in two tooth-like lobes, with a small toothlike projection on anterodistal edge of process at level of solenomere 'elbow'. + +Female slightly larger than male, legs not swollen and unusually slender. Genital aperture with posterior margin raised in low, slightly convex curve. Cyphopods not examined. + +Distribution +: Known from two disjunct areas in +New South Wales +: the Blue Mountains west of Sydney, and Mt Keira, northwest of Wollongong ( +Fig. 31 +). The gap is ca. +80 km +. + + +Etymology +: For the late Christine Horseman (d. 2006), collector of the +holotype +, a technical officer at the Australian Museum from the late 1960s to the early 1990s. + + + +FIGURE 16. + +Orthorhachis christinae + + +n. sp. + +, male paratype, AM KS94912. (A) lateral, (B) posterior, (C) medial views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + + +Remarks +: Specimens of + +O. christinae + +from the +type +locality and the Blue Mountains are smaller than those from Mt Keira. The latter also have more distinct raised areas on the metatergites and proportionally longer antennae. Nevertheless, the two populations have gonopods of the same distinctive form. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97659C1DFF06FA91FE6A07A2.xml b/data/38/2B/5C/382B5C2C97659C1DFF06FA91FE6A07A2.xml new file mode 100644 index 00000000000..12ba9cde87d --- /dev/null +++ b/data/38/2B/5C/382B5C2C97659C1DFF06FA91FE6A07A2.xml @@ -0,0 +1,821 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis durabilis + +n. sp. + + + + + + +Figs. 5D +, +7A +, +17 +; map +Fig. 31 + + + + +Holotype + +: +1 male +, +Rutherford Creek +, +Brown Mountain +near +Nimmitabel +, NSW, ca. + +820 m + +, + +26 May 1970 + +, +R +. +W. Taylor +& +R +. +Bartell +, rainforest, +ANIC +berlesates 285-6. +In +ANIC +, 64-000189. + + + + + +Paratypes + +: In +ANIC + +: + +1 male +, +Rutherford Creek +, +Brown Mountain +, NSW, + +9 January 1968 + +, +M. Upton +, rainforest, leafmould, +ANIC + +berlesate 55, 64-000187; + +3 males +, +1 female +, +Monga +, NSW, +35º35'S +149º55'E +, + +27 February 1968 + +, +M. Upton +& +L. Mound +, rainforest, +ANIC + +berlesate 72, 64-000188; + +1 male +, details as for +holotype +but +ANIC + +berlesate 287, 64-000190. + + +In MV: + +2 males +, +Cobbanah Creek +, +Vic +, +37º38'12"S +147º14'09"E +, + +320 m + +, + +25 November 2004 + +, +R + +. + +Mesibov +& +T + +. + +Moule +, K-10662, 10663 + +; +4 females +, same details, K-10664–10667; +2 males +, +3 females +, 1 stadium + +7 female +, +Uralla Nature Reserve +, +Trafalgar +, +Vic +, +38º13'55"S +146º08'40"E +, + +200 m + +, + +2 August 2005 + +, +R + +. + +Mesibov +, K-10673–10678 + +; + +1 male +, +1 female +in copula, +Buldah Gap Road +, S of +Buldah +, +Vic +, +37º18'25"S +149º09'57"E +, + +560 m + +(GE), + +10 November 2006 + +, +R + +. + +Mesibov +& +T + +. + +Moule +, K-10682, 10683 + +; +1 male +, +1 female +, same details, K- 10684, 10685. + + +Other material examined +: + +In +AM +: +1 male + +, + +Emerald district +, +Vic +, + +August 1904 + +, collector 'E.N.J.', +KS +103051; +1 male +, +1 female + +, + +ca. + +15 km +SE of Countegany + +, near + + +Two +River + +Plain + +, +Wadbilliga Trail National Park +, NSW, +36º17'50"S +149º32'32"E +, + +970 m + +, + +17 May 2006 + +, +C.A. Car +, +KS +103052 + +. + + +In MV: + +5 males +, +1 female +, near +Trafalgar +, +Vic +, + +August 1890 + +, +W. Kershaw +, K-10655 + +; + +2 males +, +Thorpdale +, +Vic +, + +1 April 1899 + +, collector unknown, K-10656 + +; +1 male +, +2 females +, 1 stadium + +7 male +, +National Park +, +Vic +, + +11 June 1932 + +, collector unknown, K-10657 + +; +2 males +, +1 female +, 1 stadium + +7 male +, +Wombargo Creek +, +Rockbank +, +Black Mountain +, +Vic +, + +30 April 1947 + +, +C. Barrett +, K-10658 + +; + +1 male +, +1 female +, +3.8 miles +E of turnoff on +Benambra-Suggan Buggan Road +, +Vic +, grid 1553(3) map ref 618434, no date or collector, snow gum stand, under logs, K-10659 + +; + +3 males +, +1 female +, +2.3 miles +from +Suggan-Buggan Road +, +Vic +, grid 1553(3) map ref 618438, no date or collector, snow gum stand, grass ground cover, under logs, K-10660 + +; +1 male +, +1 female +, grid 1553(3) map ref 616440, Vic, no date or collector, snow gum stand, K-10661; + +1 male +, +Slippery Hill +near +Dargo +, +Vic +, +37º23'05"S +147º12'54"E +, + +920 m + +, same date and collectors, K-10668 + +; +1 male +, 1 stadium + +7 male +, +Mt Buller +, +Vic +, near sewage plant, +37º08'56"S +146º27'27"E +, + +1560 m + +, + +1 January 2005 + +, +K. Bonham +, K-10669 + +; + +1 male +, +2 females +, ' +Loch Springs' +property, +Trafalagar +, +Vic +, +38º13'38"S +146º08'55"E +, + +150 m + +, same date and collector, K- 10671 + +; + +1 male +, +1 female +, +Uralla Nature Reserve +, +Trafalgar +, +Vic +, +38º13'36"S +146º08'53"E +, + +140 m + +, + +19 April 2005 + +, +R + +. + +Mesibov +, K-10670 + +; +1 male +, 1 stadium + +7 male +, +Darlimurla +, +Vic +, +38º21'58"S +146º11'05"E +, + +200 m + +, + +1 August 2005 + +, +N. Porch +& +R + +. + +Mesibov +, K-10672 + +; + +1 female +, +Sunny Creek +at +Yarragon South +, +Vic +, +38º14'54"S +146º05'31"E +, + +350 m + +, + +3 August 2005 + +, +R + +. + +Mesibov +& +J. Poppins +, K-10679 + +; + +1 male +, +Trafalgar East +, +Vic +, +38º12'54"S +146º12'32"E +, + +190 m + +, + +4 August 2005 + +, +R + +. + +Mesibov +, K-10680; 1 stadium + + +7 male +, +Yarragon South +, +Vic +, +38º15'06"S +146º06'23"E +, + +340 m + +, + +21 April 2006 + +, +R + +. + +Mesibov +, K-10681 + +; + +1 male +, +1 female +, +Nadgee State Forest +, +S of Eden +, NSW, +37º17'42"S +149º49'21"E +, + +100 m + +(GE), + +12 November 2006 + +, +C. & G. Car +, +R + +. + +Mesibov +& +T + +. + +Moule +, K-10686 + +; + +1 male +, +1 female +, +Board Road +, Mt Disappointment State Forest, +Vic +, +37º25'37"S +145º08'50"E +, + +770 m + +(GE), + +20 September 2007 + +, +R + +. + +Mesibov +, K-10687 + +. + + +In WAM: + +1 male +, 1 stadium +6 female +, 'The Beeches', Vic, +37º28'S +145º49'E +, + +25 March 1991 + +, +M.S. Harvey +& +M.E. Blosfelds +, +T +73068 + +. + + +Diagnosis +: Paranota very wide (midbody paranota width twice as great as ring width), metatergites with Pattern B sculpture. Gonopod telopodite with solenomere and medial process well separated, the latter expanded distally and terminating in a wide truncation, with the anterior corner produced as a small distal tooth. + + +Description +: As for the genus. Male/female approximate measurements: length 18/ +20 mm +, midbody prozonite diameter 1.5/ +1.8 mm +, midbody width across paranota 3.0/ +3.2 mm +. Colouring variable in alcohol, ranging from near-uniform grey-brown to medium brown with paler mottling. Antennal sockets separated by 1.5X a socket diameter. Antennae short, stouter than in other + +Orthorhachis + +, relative lengths of antennomeres (2,6)>3>(4,5). Collum D-shaped with posterior margin slightly emarginate on either side, slightly wider than head and narrower than tergite 2. Metatergite sculpture very distinct, Pattern B ( +Fig. 7A +). Paranota very wide,anterior margin sloping posterolaterally to distinct corner, lateral margin more or less parallel to long axis of body; ozopore between one-half and two-thirds the length of the lateral margin ( +Fig. 7A +). Legs short, leg 6 tarsus 1.2X as long as femur ( +Fig. 5D +). Brush setae with forked tips. + + +Gonopod aperture ovoid, wider than long, about one-third the width of the ring 7 prozonite, rim raised posterolaterally. Telopodite ( +Fig. 17 +) short, broad at base, tapering distally; long setae on posterolateral surface to one-third telopodite height; branching beginning at two-thirds telopodite height. Solenomere a slightly tapering rod with a bluntly pointed tip, directed distally and slightly posteriorly, slightly S-shaped in lateral view (right gonopod). Medial process well-separated from solenomere, broader than solenomere at base, expanding distally and mediolaterally flattened, ending at half solenomere height in a wide truncation with a posterior corner which extends further posteriorly than solenomere in lateral view, and with a small distal tooth at anterior end of truncation. + + + +FIGURE 17. + +Orthorhachis durabilis + + +n. sp. + +, male paratype, MV K-10662. (A) medial, (B) anterior, (C) lateral views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + +Female slightly larger than male, legs not swollen. Genital aperture with posterior margin raised in slightly convex curve, bent slightly anteriorly. Cyphopods not examined. + +Distribution +: From near sea level to at least +1560 m +over ca. +60000 km + +2 +in + +eastern +Victoria +and far southeastern +New South Wales +( +Fig. 31 +). I have collected + +O. durabilis + +under loose bark on logs, in leaf litter and under pieces of rotting wood on the ground. + + +Etymology +: Latin + +durabilis + +, lasting, adjective, for the persistence of this species in farmed landscapes in the West Gippsland district of +Victoria +. + + +Remarks +: Ignoring gonopod structure, this species would not readily be recognised as an + +Orthorhachis + +: the tarsi are short and the paranota are remarkably wide and narrow. The gonopods, however, conform to the + +Orthorhachis + +pattern and are similar to those of + +O. tallagandensis + +and + +O. weiri + +, which have long tarsi and more typically shaped and sized paranota. + + + +O. durabilis + +varies little over its remarkably large range: specimens from Monga and Mt Disappointment State Forest, ca. +450 km +apart, are virtually identical. On the gonopod telopodite, there is minor variation in the depth of the branching and in the degree of overall taper. + + +This species is unusual among southeastern Australian dalodesmids for its apparent tolerance of habitat disturbance. In +Victoria +, I have found it in degraded bush remnants, on roadsides and on the margins of pasture adjoining forest. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97699C11FF06F918FE4C07AF.xml b/data/38/2B/5C/382B5C2C97699C11FF06F918FE4C07AF.xml new file mode 100644 index 00000000000..3dd01215c63 --- /dev/null +++ b/data/38/2B/5C/382B5C2C97699C11FF06F918FE4C07AF.xml @@ -0,0 +1,204 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis celtica + +n. sp. + + + + + + +Fig. 15 +; map +Fig. 32A + + + + +Holotype + +: +Male. Oakes State Forest +, +Horseshoe Road +, + +2 km +NNE of Killekrankie Mountain + +, NSW, +30º31'22"S +152º32'59"E +, + +760 m + +(GE), + +11–24 November 1999 + +, +M. Gray +, +G. Milledge +& +H. Smith +, +pit traps +, +Hotspots NE +NSW site 16. +In +AM +, +KS61556 +; anterior rings in genitalia vial. + + + + +FIGURE 14. + +Orthorhachis cavatica +Jeekel, 2006 + +, male holotype; redrawn and simplified from Jeekel (2006). (A) medial, (B) posterior views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. + + + + + +Paratype + +: In +AM +: +1 male + +, + +Belbucca Road +, +Irishman State Forest +, NSW, +30º32'58"S +152º40'14"E +, + +520 m + +(GE), + +11–24 November 1999 + +, +G. Milledge +& +H. Smith +, +pit traps +, +KS +103046 + +. + + +Other material examined +: None available. + + +Diagnosis +: Gonopod telopodite with solenomere strongly tapering from wide base, and with third telopodite process on anterior surface, the process partly enclosed within fold of medial branch of telopodite and with small lateral teeth. + + +Description +: As for the genus. Male approximate measurements: length +14 mm +, midbody prozonite diameter +1.3 mm +, midbody width across paranota +1.8 mm +. Body discoloured, near-uniform light brown. Antennal sockets separated by 2.5X a socket diameter. Antennae slender, relative lengths of antennomeres 3>(2,6)>(4,5). Collum D-shaped with rounded corners, narrower than head and tergite 2. Metatergite sculpture very indistinct, possibly Pattern A. Paranota with anterior margin convex, lateral margin more or less parallel to long axis of body. Legs slender, leg 6 tarsus 1.7X as long as femur. Brush setae with forked tips. + + +Gonopod aperture ovoid, slightly wider than long, about one-third the width of the ring 7 prozonite, rim raised posterolaterally. Telopodite ( +Fig. 15 +) short, broad at base, swollen laterally and posteriorly at one-third to one-half telopodite height; sparse long setae on posterolateral surface to one-third telopodite height; branching beginning at two-thirds telopodite height. Solenomere broad at base, directed slightly posteriorly, rapidly tapering at half solenomere height and curving laterally, with a small tooth-like projection on distomedial surface just below tip. Medial process well-separated from solenomere, slightly C-shaped (concave posteriorly), expanded just above base and somewhat flattened mediolaterally, folded to partly enclose third telopodite process laterally; distally truncate and terminating just proximal to solenomere tip, with a small, short posterior projection at about three-quarters length of medial process. Third telopodite process rod-like, bluntly pointed, with lateral edge produced near base; arising just medial and basal to medial process origin with cuticular ridge extending basally on anteromedial surface of telopodite; process directed parallel to solenomere and terminating at about half solenomere height; with minute teeth on anterolateral surface to onethird process height; partly enclosed medially by fold of medial process. Prostatic groove running laterodistally for short distance on anterior surface of telopodite, then turning distally before running laterodistally lateral to third telopodite process to solenomere base, then following curves of solenomere to tip. + +Female not yet recognised. + + +FIGURE 15. + +Orthorhachis celtica + +n. sp. +, male paratype, AM KS103046. (A) medial, (B) posterior and slightly lateral, (C) lateral, (D) anterior views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + + +Distribution +: Known only from two sites ca. +12 km +apart, south of Dorrigo in northeastern +New South Wales +, between localities for + +O. kerewong + +and + +O. serrata + +( +Fig. 32A +) + + +Etymology +: Latin +celticus +, of the Celts, adjective, for the two known localities, Irishman State Forest and Killekrankie Mountain. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97699C13FF06FD75FC6806F4.xml b/data/38/2B/5C/382B5C2C97699C13FF06FD75FC6806F4.xml new file mode 100644 index 00000000000..5b0c2c1b2fb --- /dev/null +++ b/data/38/2B/5C/382B5C2C97699C13FF06FD75FC6806F4.xml @@ -0,0 +1,140 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis cavatica +Jeekel, 2006 + + + + + + + +Fig. 14 +; map +Fig. 31 + + + + + +Orthorhachis cavatica +Jeekel, 2006:74 + +, +Figs. 4–6 +. + + + + + +Holotype + +: Male. Tricketts Cave, Yarrangobilly, NSW, +13 April 1971 +, E. Hamilton-Smith, field code BS2103. Not examined. + + + +Paratypes + +: +1 male +, +3 females +, details as for +holotype +. Not examined. + + +Other material examined +: None available. + + +Diagnosis +: Gonopod telopodite with solenomere well-separated from medial process, the latter terminating in three lobes, the anterior lobe most distal and distally crenulate. + + +Description +: The following brief notes are based on the description given by Jeekel (2006), with direct quotes as indicated. Male/female approximate measurements: width across paranota 2.4/ +2.8 mm +. Body 'brownish-pinkish white'. Antennal sockets separated by 1.5X a socket diameter. Antennae long, 'length of 6th to 8th antennomeres combined almost as long as the 3rd'. Collum 'a little narrower than the head and the 3rd somite, subreniform in dorsal outline.' 'Surface of metatergites in middle part of the body along the posterior margin with 5+5 longitudinal ribs, each bearing a faint wart. Before this zone, behind the transverse furrow, the surface is uneven and has 4+4 indistinct warts.' Paranota with lateral margin 'widely convex'. Legs slender, leg on ring 7 with tarsus 1.7X as long as femur (Jeekel 2006, +Fig. 4 +). Gonopod telopodite as shown ( +Fig. 14 +); this figure was redrawn from Jeekel (2006, +Figs. 5 +, +6 +). Female genital aperture with posterior margin 'raised, widely and weakly concave, but without median projection between the coxae.' + + +Distribution +: Known only from the +type +locality in Kosciuszko National Park, southeastern +New South Wales +, close to one of the + +O. catherinae + +localities ( +Fig. 31 +). + + +Remarks +: The +types +of + +O. cavatica + +and + +O. paradoxalis + +are among specimens on loan from +SAM +(Jeekel, 2006) and were not available for study. However, it seems clear from Jeekel's description (quoted above) that the metatergite sculpturing in this species conforms to Pattern A. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C976C9C16FF06FD75FE590704.xml b/data/38/2B/5C/382B5C2C976C9C16FF06FD75FE590704.xml new file mode 100644 index 00000000000..d5a217d1fd8 --- /dev/null +++ b/data/38/2B/5C/382B5C2C976C9C16FF06FD75FE590704.xml @@ -0,0 +1,170 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Gephyrodesmus regilacus + +n. sp. + + + + + + +Fig. 11 +; map +Fig. 12 + + + + +Holotype + +: Male. Board Road, +Mt Disappointment State Forest +, +Vic +, +37º25'37"S +145º08'50"E +, + +730 m + +, + +20 September 2007 + +, +R +. Mesibov. In +MV +, K-10639. + + + + +Paratypes + +: In + +MV +: +1 male +, +1 female +, +Belgrave West +, +Vic +, + +November 1930 + +, +J. Clark +, K-10636, 10637 + +; + +1 male +, +Kinglake National Park +, +Vic +, + +28 October 1983 + +, 'M.F.N.C.', +pitfall trap +, K-10638 + +; +1 male +, +1 female +, details as for +holotype +, K-10640, 10641. + + +Other material examined +: None available. + + +Diagnosis +: Medial branch of gonopod telopodite divided into two subequal, bluntly rounded tips; anterior edge of ring 7 aperture well separated from anterior edge of prozonite; metatergite sculpture hard to see. + + +Description +: As for the genus. Male/female approximate measurements: length 19/ +20 mm +, midbody prozonite diameter 1.8/ +1.9 mm +, midbody width across paranota 2.5/ +2.7 mm +. In alcohol, well-coloured (Board Road) specimens mainly light greyish-brown with complex pattern of small, pale patches; antennae and distal podomeres darker. Antennal sockets separated by ca. 2X a socket diameter. Collum wider than head, narrower than tergite 2, D-shaped with the posterior margin slightly indented on either side. Raised areas on metatergites, except for posterior lateral area (extending onto posterior paranotal corner) very low, poorly defined. Gonopod aperture about one-third width of prozonite, ovoid, slightly wider than long, anterior edge well separated from anterior edge of prozonite, lateral edge raised posteriorly. + + +Gonopod telopodite ( +Fig. 11 +) base wider than long; long setae on posterolateral surface to level of branching at about one-third telopodite height. Solenomere a slightly tapering cylinder at base, directed distally and slightly posteriorly; abruptly tapering at about three-quarters the telopodite height and curving slightly anteromedially, the tip narrow and shallowly notched. Medial branch stouter than solenomere, curving slightly posteriorly near apex, branching at level of solenomere bend into more or less equal lateral and medial tips, both tapering and bluntly rounded, terminating no further posteriorly than the solenomere bend. + +Female slightly larger than male, legs not swollen. Genital aperture with posterior margin raised as long, low, straight-edged flange, just over one-third the metazonite diameter. Cyphopods not examined. + +Distribution +: Known from eucalypt forest at three localities in central +Victoria +( +Fig. 12 +). At the +type +locality, found on the underside of small pieces of rotting wood on the ground. + + +Etymology +: Latin +regis +, king, + +lacus +, lake, noun in apposition, for Kinglake National Park, one of the localities for this species. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C976E9C15FF06FAA1FE8D0662.xml b/data/38/2B/5C/382B5C2C976E9C15FF06FAA1FE8D0662.xml new file mode 100644 index 00000000000..d8b2e142ef1 --- /dev/null +++ b/data/38/2B/5C/382B5C2C976E9C15FF06FAA1FE8D0662.xml @@ -0,0 +1,208 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis +Jeekel, 1985 + + + + + + + + + + +Orthorhachis +Jeekel, 1985:51 + + +. + +Shelley et al., 2000:118 + +. + + + + + + +Type +species + +: + +O. pallida +Jeekel, 1985 + +, by original designation. + + +Diagnosis +: H+20 +Dalodesmidae +with tarsus 1.2–2.0 times as long as prefemur, forked tips or a mid-length branch on brush setae, and gonopod telopodite divided into two small branches: a lateral solenomere and a medial process not reaching as far distally as the solenomere tip (except in + +O. vinnula + +n. sp. +). Distinguished from + +Tasmanodesmus + +by the presence in the latter of a third telopodite process lateral to the solenomere and by the presence in + +Orthorhachis + +of low, discrete, raised areas on the metatergites. Distinguished from + +Gephyrodesmus + +by the branching into solenomere and medial process beginning at more than half the telopodite height in + +Orthorhachis + +, and at one-third or less the telopodite height in + +Gephyrodesmus + +. + + +Description +: Head with frons and vertex moderately setose, vertex less so; vertigial sulcus usually distinct, reaching to about two-thirds the distance from top of vertex to top of antennal sockets. Tergite widths usually increasing from rings 2 to 5 or 6, about equal from 5 or 6 to17; tergite 3 usually shorter than 2 or 4. Waist usually without longitudinal striations; limbus composed of long, narrow, flat tabs with irregularly toothed ends. Metatergites and paranota with low, discrete, raised areas in Patterns A or B (see metatergite sculpture section, above). Paranota with anterior margin slightly upturned and partly roughened; lateral margin dipping anteriorly in lateral view, usually with a few small notches on midbody rings, each with a minute seta on anterior corner of notch; posterior paranotal corners weakly produced as broad, bluntly rounded projections, flat in lateral view, the projections increasing slightly in length from anterior to posterior; posterior margin minutely and irregularly serrate. Spiracles small, openings round or slightly elliptical, only slightly raised above pleural surface; on diplosegments with anterior spiracle just anterior of coxal midline above a small projecting shelf of cuticle, posterior spiracle about midway between leg-bases. Pore formula 5, 7, 9, 10, 12, 13, 15–19; ozopore opening dorsolaterally close to paranotal margin and just lateral to raised areas, usually near posterior corner at three-quarters to seven-eighths the length of paranotum. Sternites sparsely setose, slightly wider than long or as wide as long, transverse impression deeper than longitudinal ( +Fig. 4A +). Legs ( +Figs. 5C, 5D, 5E +) slender; prefemur swollen dorsally, femur slightly so, swelling greatest on anterior legs; tarsus long, thin, slightly curved; relative podomere lengths tarsus>femur>prefemur>(postfemur, tibia). Numerous sphaerotrichomes on tarsus and tibia of anterior legs, hemispherical with sharp-pointed, tapered setal shaft inclined distally and slightly outwards. Preanal ring sparsely setose; hypoproct paraboloid or trapezoidal with rounded corners; epiproct bluntly rounded, extending past anal valves. Male with small gonopore opening ventrally on swelling of leg 2 coxa, not on prominent raised cone. Gonocoxae setose distally on anterolateral and posteromedial surfaces, somewhat concave medially, weakly joined anteromedially. Cannula prominent, inserting anteromedially on telopodite. Telopodites short, when retracted extending to leg 6 coxae; leg 7 coxae well separated, leg 6 coxae much less so. Prostatic groove running laterodistally on anterior surface of telopodite base before curving distally, then laterodistally and following solenomere to tip. + + +Distribution +: Forest and woodland in higher-rainfall areas of southeastern +Australia +, from central +Victoria +to southeastern +Queensland +( +Figs. 31 +, +32 +) + + +Remarks +: The gender of the genus is feminine. In +Jeekel (1985) +the +type +species name + +pallida + +is spelled correctly in the main text but incorrectly +pallidus +in the caption to figures (p. 53). + + + +Orthorhachis + +as here circumscribed is a heterogeneous taxon with several species, e.g. + +O. durabilis + +n. sp. +and + +O. weiri + +n. sp. +, looking very unlike the +type +species in non-gonopodal features. I am reluctant to erect new genera for such species at this time, given the overall uniformity in gonopod structure in the 18 species included below. Relationships within + +Orthorhachis + +may become clearer in future when genetic studies of the group are carried out. + + +The median tab on posterior sternites ( +Figs. 4A, 4B +) is an interesting synapomorphy of + +O. catherinae + +n. sp. +, + +O. paradoxalis +Jeekel, 2006 + +and + +O. tallagandensis + +n. sp. +The three species all occur in the same part of +New South Wales +and further collecting may show that they are parapatric. Whether a fourth species from the area, + +O. cavatica +Jeekel, 2006 + +, also has this character is not yet known. Jeekel (2006) does not mention sternite cones or tabs in his descriptions of either + +O. cavatica + +or + +O. paradoxalis + +, and I was unable to examine the + +O. cavatica + +types +. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C976F9C13FF06F9B5FB130222.xml b/data/38/2B/5C/382B5C2C976F9C13FF06F9B5FB130222.xml new file mode 100644 index 00000000000..960ca3d2333 --- /dev/null +++ b/data/38/2B/5C/382B5C2C976F9C13FF06F9B5FB130222.xml @@ -0,0 +1,193 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Orthorhachis catherinae + +n. sp. + + + + + + +Figs. 6C +, +13 +; map +Fig. 31 + + + + +Holotype + +: +Male. Kosciuszko National Park +, NSW, +1 km +NW of junction of +Long Plain Road +and + + +Snowy +Mountain + +Highway + +, +35º42'49"S +148º31'26"E +, + +1320 m + +, edge of forest/alpine vegetation boundary, in fine leaf litter, + +14 November 2006 + +, +C.A. Car. In +AM +, +KS +103044. + + + + + +Paratypes + +: In +AM +: +1 male + +, + +Mt Kosciuszko +, NSW, + +9 February 1979 + +, +D.K. McAlpine +& +B.J. Day +, +KS36825 +; +1 male + +, + +details as for +holotype +, +KS +103045 + +. + + +Other material examined +: None available. + + +Diagnosis +: Gonopod telopodite with solenomere divided into mediolaterally expanded basal section and narrow distal section, and with medial process bearing a short posterior projection with expanded tip. Posterior sternites with median tab-like structure along posterior edge. + + +Description +: As for the genus. Male approximate measurements: length +21 mm +, midbody prozonite diameter +1.7 mm +, midbody width across paranota +2.4 mm +. +Holotype +near-uniform medium brown. Antennal sockets separated by just under 2X a socket diameter. Antennae slender, relative lengths of antennomeres (2,3)>5>(4,6). Collum D-shaped with slightly produced posterior corners; wider than head but narrower than tergite 2. Metatergite sculpture distinct, Pattern A ( +Fig. 6C +). Paranota with anterior and lateral margins forming a single smooth, convex curve ( +Fig. 6C +). Legs slender, leg 6 tarsus 1.7X as long as femur. Brush setae with forked tips. Sternites of posterior rings (10–18?) with a small, median, rounded, two-lobed tab on posterior edge, less evident on anterior rings in the tab-bearing set. + + + +FIGURE 13. + +Orthorhachis catherinae + + +n. sp. + +, male paratype, AM KS103045. (A) lateral, (B) anterior, (C) medial, (D) posterior views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + + +Gonopod aperture ovoid, slightly wider than long, about one-third the width of the ring 7 prozonite, rim raised posterolaterally. Telopodite ( +Fig. 13 +) short, proximal portion cylindrical, slightly flared at base; long setae on posterolateral surface to just over one-third telopodite height; branching beginning at between onehalf and two-thirds telopodite height. Basal section of solenomere bending slightly posteriorly at base, swelling medially and laterally to about half telopodite width. Distal section of solenomere arising from posterolat- eral corner of swollen tip of basal section, narrow, cylindrical and tapering, bending first posteriorly and laterally and curving anteriorly, then posteriorly near the tip, the posterior surface roughened on the anterior curve. Medial process cylindrical at base, as wide as solenomere and well-separated from it, C-shaped (concave posteriorly); expanded at tip with broad, shallow, terminal depression; terminating at about two-thirds height of distal section of solenomere; with narrow rod-like projection arising at about two-thirds medial process height, directed posteriorly and slightly laterally, slightly expanded at tip, terminating posteriorly no further than anterior curve of distal solenomere section. + +Female not yet recognised. + +Distribution +: Known only from two high-elevation sites in Kosciuszko National Park, southeastern +New South Wales +( +Fig. 31 +). One site is close to the only known + +O. cavatica + +locality. + + +Etymology +: For Catherine Car, student of +Paradoxosomatidae +and collector of the +holotype +. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97709C08FF06F98BFD7A06AC.xml b/data/38/2B/5C/382B5C2C97709C08FF06F98BFD7A06AC.xml new file mode 100644 index 00000000000..7eb5a18ae5f --- /dev/null +++ b/data/38/2B/5C/382B5C2C97709C08FF06F98BFD7A06AC.xml @@ -0,0 +1,655 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Gephyrodesmus cineraceus +Jeekel, 1983 + + + + + + + +Figs. 1D +, +3C +, +5B +, +9 +; map +Fig. 12 + + + + + + + +Gephyrodesmus cineraceus +Jeekel, 1983:146 + + +, +Figs. 1–3 +; 1985 50. + + +Shelley +et al +., 2000:102 + + +. + +Mesibov 2004b:42 + +. + + + + + + + +Holotype + +: +Male. Drummer State Forest +, + +15 km +E of Cann River + +, +Vic +, + +13 November 1980 + +, +C.A.W. Jeekel +and +A.M. Jeekel-Rijvers +, eucalypt forest along +Princes Highway +, under logs, +Australia +Expedition station +84. +Possibly in Zoological Museum +, +Amsterdam +; not examined. + + + + +Paratypes + +: None. + + +Other material +: In +AM +: + +1 male +, +Brown Mountain +, +Nimmitabel +, NSW, +36º35'S +149º23'E +, + +4000 ft + +, + +30 August 1966 + +, +P.M. Johns +, dense wet sclerophyll, +KS94164 + +; + +1 male +, +Nowra Weta Cave +, NSW, +34º50'S +150º30'E +, + +20 February 1977 + +, +G. Campbell +, +KS10842 + +; + +3 males +, +Tidbinbilla Nature Reserve +, ACT, +35º28'S +148º52'E +, + +9 March 1978 + +, +P. Ormay +, +pitfall trap +, FN2417, +KS +103038 + +; + +3 males +, +1 female +, +Forest Drive +, +Kioloa State Forest +, + +18 km +N of Batemans Bay + +, NSW, +35º37'S +150º16'E +, + +19 October 1978 + +, +C. Horseman +, litter, FN1205, +KS +103039 + +; + +1 male +, +1 female +, +Kioloa State Forest +rest area, NSW, + +22 November 1979 + +, +C. Horseman +, +KS36821 + +; + +6 males +, +1 female +, +Forest Drive +, +Kioloa State Forest +, NSW, + +22 December 1979 + +, +C. Horseman +, +KS36822 + +; + +4 males +, +1 female +, +Jamberco Mountain +via +Kiama +, NSW, +34º40'S +150º43'E +, + +8 November 1987 + +, +G.S. Hunt +& volunteer staff, rainforest, hand sorting, leaf litter, +KS17932 + +; + +1 male +, +Nerrigundah Mountain +Road, approx. +2.25 km +E of junction with +Cadgee Mountain +Road, +Dampier State Forest +, NSW, +36º08'13"S +149º57'18"E +, + +90 m + +(GE), + +10 March 1999 + +, +J. Tarnawski +& +S. Lassau +, +pit trap +, +CBCR003-009 +, +KS93257 + +; + +1 male +, +Bodalla State Forest +, Tuross +River Road +, NSW, +36º11'16"S +149º56'16"E +, + +180 m + +(GE), + +10 March 1999 + +, +L. Wilkie +& +R + +. + +Harris +, +KS +103040 + +; + +1 male +, +Ross Rixon Road +, +2.5 km +SE from junction with +Little Sugarloaf Road +, +Dampier State Forest +, NSW, +36º02'56"S +149º57'21"E +, + +90 m + +(GE), + +11 March 1999 + +, +L. Wilkie +& +R + +. + +Harris +, +pit trap +, +CBCR003-078 +, +KS93235 + +; + +1 male +, + +300 m + +S of junction of +North Head +and Carls +Mountain Roads +, +Murramarang National Park +, NSW, +35º41.15'S +150º15.72'E +, + +17 March 1999 + +, +L. Wilkie +& +R + +. + +Harris +, litter, +CBCR003-117 +, +KS66899 + +; +1 male +, 1 stadium + +7 male +, same date and collectors but +North Head Road +, approx. + +300 m + +N of junction with +Carls Mountain +Road, +Murramarang National Park +, NSW, +35º40.85'S +150º15.88'E +, litter, +CBCR003-119 +, +KS66907 + +; + +1 male +, same date and collectors but +1.6 km +along Richmond +Beach Road +from junction with +North Head Road +, +Murramarang National Park +, NSW, +35º40.85'S +150º17.03'E +, litter, +CBCR003-115 +, +KS66918 + +. + + +In +ANIC +: + +1 male +, +Brown Mountain +, +Rutherford Creek +, NSW, +36º36'S +149º23'E +, + +9 December 1967 + +, +R + +. + +W. Taylor +& C. +Brooks +, +ANIC + +berlesate 41, leafmould, 64-000183; + +2 males +, +1 female +, +Kangaroo Valley +, NSW, +34º44'S +150º32'E +, + +3 December 1983 + +, +R + +. + +J. +Moran +, +ANIC + +berlesate 892, leaf litter, 64-000184; + +3 males +, +2 females +, +Tallaganda State Forest +, + +10 km +S of Captains Flat + +, NSW, +35º41'S +149º26'E +, + +3 December 2005 + +, +C. Car +& +R + +. + +Mesibov +, 64-000185 + +. + + +In +MV +: + +1 male +, +1 female +, +Marriotts Creek +, +Vic +, no date, no collector, ' +Ref +: - 178.411', + +900 m + +(GE), open dry forest, K-10634 + +; + +1 male +, +Dyer Creek +, near +Murrungowar +, +Vic +, +37º38'26"S +148º43'24"E +, + +140 m + +, + +8 November 2006 + +, +R + +. + +Mesibov +& +T + +. + +Moule +, K-10635 + +. + + +Diagnosis +: Medial branch of gonopod telopodite nearly uniform in width in medial or lateral view, with most distal point marked by small, rounded projection; anterior edge of ring 7 aperture adjoining anterior edge of prozonite; metatergite sculpture well-defined. + + +Description +: +Jeekel (1983) +gives a very detailed description of the + +G. cineraceus + +holotype +, and the following notes and accompanying illustrations are given here only for the sake of consistency. + + +Male/female approximate measurements: length 18/ +19 mm +, midbody prozonite diameter 1.4/ +1.5 mm +, midbody width across paranota 2.4/ +2.5 mm +. In alcohol, well-coloured specimens light greyish-brown. Antennal sockets separated by ca. 2X a socket diameter. Collum about as wide as head, D-shaped, slightly narrower than tergite 2. Raised areas on metatergites low but distinct. Gonopod aperture about one-half width of prozonite, ovoid, longer than wide, anterior edge adjoining anterior edge of prozonite, lateral edge raised posteriorly. + + +Gonopod telopodite ( +Fig. 9 +) with very low base, somewhat expanded laterally and medially near junction with gonocoxa; long setae on posterolateral surface to level of branching at between one-quarter and one-third telopodite height. Solenomere massive at base, somewhat swollen posteriorly and medially, abruptly tapering at about half telopodite height, the distal portion bending posterolaterally before abruptly turning distally at 'elbow' and curving slightly medially, near the tip narrowing and bending slightly anteriorly. Medial branch Cshaped from base (concave posteriorly) and much narrower than solenomere at base, slightly flattened mediolaterally, with a small, basally directed projection on lateral surface just distal to solenomere 'elbow'; at top of 'C', at about half the height of distal portion of solenomere, bending posterobasally and slightly laterally, with a small, rounded projection on anterior (distal) surface at bend; terminating at level of solenomere 'elbow' in mediolaterally flattened, slightly expanded portion, truncated basally. + +Female slightly larger than male, legs not swollen. Genital aperture with posterior margin not significantly raised. Cyphopods not examined. + + +FIGURE 9. + +Gephyrodesmus cineraceus +Jeekel, 1983 + +, male, MV K-10635. (A) anterior, (B) anterolateral, (C) lateral views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + + +Distribution +: In forest from near sea level to at least +1200 m +over ca. +25000 km + +2 +in + +New South Wales +and +Victoria +( +Fig. 12 +). Found under logs at the +type +locality, in rotting wood at the Tallaganda State Forest site and in leaf litter at the Dyer Creek site. + + +Remarks +: This species varies a little in size over its large geographic range, but is otherwise very consistent in body characters and gonopod details. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97729C16FF06F8C3FB530222.xml b/data/38/2B/5C/382B5C2C97729C16FF06F8C3FB530222.xml new file mode 100644 index 00000000000..c1cbc1186bc --- /dev/null +++ b/data/38/2B/5C/382B5C2C97729C16FF06F8C3FB530222.xml @@ -0,0 +1,167 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Gephyrodesmus coolahensis + +n. sp. + + + + + + +Fig. 10 +; map +Fig. 12 + + + + +Holotype + +: +Male. Coolah Tops National Park +, NSW, +31º43'59"S +150º02'04"E +, + +1100 m + +(GE), + +7–25 November 2001 + +, +M. Gray +, +G. Milledge +& +H. Smith +, +pitfall +. +In +AM +, +KS +103041, dissected, stored in three genitalia vials. + + + + + +Paratypes + +: In +AM +: +2 females + +, + +details as for +holotype +, +KS +103042 + +. + + +Other material examined +: None available. + + +Diagnosis +: Medial branch of gonopod telopodite with distal portion well-defined by abrupt constriction, and with tip expanded; short, spike-like process between solenomere and medial branch; anterior edge of ring 7 aperture well separated from anterior edge of prozonite; metatergite sculpture hard to see. + + +Description +: As for the genus. Male/female approximate measurements: length 11/ +11 mm +, midbody prozonite diameter 1.1/ +1.1 mm +, midbody width across paranota 1.6/ +1.5 mm +. In alcohol, +holotype +mainly chestnut brown with complex pattern of small, pale patches. Antennal sockets separated by ca. 2.5X a socket diameter. Collum narrower than head and tergite 2, D-shaped with posterior margin slightly convex. Raised areas on metatergites, except for posterior lateral area (extending onto posterior paranotal corner) very low, poorly defined. Gonopod aperture about one-third prozonite width, ovoid, wider than long, anterior edge well separated from anterior edge of prozonite, lateral edge raised posteriorly. + + + +FIGURE 10. + +Gephyrodesmus coolahensis + + +n. sp. + +, male holotype, AM KS103041. (A) anterior, (B) lateral, (C) posterior, (D) medial views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + + +Gonopod telopodite ( +Fig. 10 +) with base expanding distally above a shallow posterior constriction, long setae on posterolateral surface to level of branching at about one-third telopodite height. Solenomere massive at base, bending slightly laterally, abruptly tapering at about two-thirds telopodite height above a small, distally directed, flange-like projection on posterior surface; solenomere then curving posteromedially before abruptly turning distally at 'elbow', tapering and curving slightly anteriorly, the tip small and blunt. Medial branch C-shaped from base (concave posteriorly), somewhat flattened mediolaterally, abruptly narrowing just posterior to solenomere and proximal to solenomere tip, then curving basally and terminating in a mediolaterally flattened plate at the level of the solenomere 'elbow', the plate with one anterior and two basal marginal teeth, a fourth marginal tooth on posterior surface of narrowed portion of the medial branch at the abrupt narrowing, all four teeth small and rounded. Between solenomere and medial branches a small spike-like process with a blunt tip, directed distally, bending slightly anteromedially and terminating just proximal to the solenomere 'elbow'. + +Female not noticeably larger than male, legs not swollen. Genital aperture with posterior margin raised as long, low, straight-edged flange, just over one-third the metazonite diameter, the anterior edge slightly scalloped on either side of the midline. Cyphopods not examined. + +Distribution +: Known only from the +type +locality, southwest of Tamworth in northeastern +New South Wales +( +Fig. 12 +). The Coolah Tops carry tall, open eucalypt forest (NSW +National Parks and Wildlife Service 2002 +). + + +Etymology +: For the Coolah Tops portion of the +Liverpool +Range in +New South Wales +. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97769C0DFF06FE98FBA60282.xml b/data/38/2B/5C/382B5C2C97769C0DFF06FE98FBA60282.xml new file mode 100644 index 00000000000..1bc4768bc9e --- /dev/null +++ b/data/38/2B/5C/382B5C2C97769C0DFF06FE98FBA60282.xml @@ -0,0 +1,183 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Gephyrodesmus +Jeekel, 1983 + + + + + + + + + + +Gephyrodesmus +Jeekel, 1983:145 + + +; + +1985:50 + +. + +Shelley et al., 2000:102 + +. + + + + + + +Type +species + +: + +G. cineraceus +Jeekel, 1983 + +by original designation. + + +Diagnosis +: H+20 +Dalodesmidae +with tarsus up to 1.5–1.7X as long as femur, forked tips on brush setae, dorsal spinnerets not enclosed and gonopod telopodite divided into two large branches: a lateral solenomere bent or curving posteriorly and turning abruptly distally at a distinct 'elbow', and a medial process curving posteriorly and not reaching as far distally as the solenomere tip. Distinguished from + +Tasmanodesmus + +by the presence in the latter of a third telopodite process lateral to the solenomere and by the presence in + +Gephyrodesmus + +of discrete raised areas on the metatergites. Distinguished from + +Orthorhachis + +by the branching into solenomere and medial process beginning at more than half the telopodite height in + +Orthorhachis + +, and at onethird or less the telopodite height in + +Gephyrodesmus + +. + + +Description +: Head with frons and vertex moderately setose, vertex less so. Antenna slender, relative antennomere lengths (2,3)>6>(4,5), antennomere 6 widest. Tergite widths increasing gradually from rings 2– 5, about equal from 5–17; tergites 3, 4 shorter than 2 and 5; posterior paranotal corners produced beginning tergite 2. Waist without prominent longitudinal striations; limbus composed of long, narrow, flat tabs with irregularly toothed ends. Metatergites and paranota with low, discrete, raised areas in Pattern A (see metatergite sculpture section, above), most bearing a small seta in posterior half. Paranota with slightly convex anterior edge and variably well-defined anterior 'shoulder' with slightly upturned, partly roughened margin; lateral margin more or less straight and parallel to body, dipping anteriorly in lateral view, with 3–5 small notches, each with a minute seta on anterior corner of notch; posterior paranotal corners produced as broad, bluntly rounded projections, flat in lateral view, the projections increasing gradually in length from anterior to posterior; posterior margin minutely and irregularly serrate. Spiracles small, openings slightly elliptical, only slightly raised above pleural surface; on diplosegments with anterior spiracle just anterior of coxal midline above a small projecting shelf of cuticle, posterior spiracle about midway between leg-bases. Pore formula 5, 7, 9, 10, 12, 13, 15–19; ozopore opening dorsolaterally close to paranotal margin and just lateral to raised areas, near posterior corner at three-quarters the length of paranotum. Sternites variably setose, slightly longer than wide or as long as wide, transverse impression deeper than longitudinal. Legs ( +Fig. 5B +) slender; prefemur swollen dorsally, femur slightly so, swelling greatest on anterior legs; tarsus long, thin, slightly curved, up to 1.5–1.7X as long as femur; relative podomere lengths tarsus>>femur>prefemur>>(postfemur, tibia). Numerous sphaerotrichomes on tarsus and tibia of anterior legs, hemispherical with sharp-pointed, tapered setal shaft inclined distally and slightly outwards; at least some brush setae on basal podomeres with obviously forked tips ( +Fig. 1D +). Preanal ring sparsely setose; hypoproct paraboloid; epiproct bluntly rounded, extending well past anal valves; dorsal spinnerets set on dorsal rim of low-walled cavity containing ventral spinnerets ( +Fig. 3C +). Male with small gonopore opening ventrally on swelling of leg 2 coxa, not on prominent raised cone. Gonocoxae setose distally on anterolateral and posteromedial surfaces, somewhat concave medially, weakly joined anteromedially. Cannula prominent, inserting anteromedially on telopodite. Telopodites short, when retracted extending to leg 6 coxae; leg 7 coxae well separated, leg 6 coxae slightly separated. Prostatic groove running laterodistally on anterior surface of telopodite base before curving distally and following solenomere to tip. + + +Distribution +: Forest in higher-rainfall areas of southeastern +Australia +, from central +Victoria +to eastern central +New South Wales +( +Fig. 12 +). + + +There is a ca. +300 km +gap between known localities for the two +New South Wales +species of + +Gephyrodesmus + +. However, southeastern +New South Wales +has not yet been well surveyed for dalodesmids, and the gap may be a sampling artifact. Northeastern +New South Wales +and far southeastern +Queensland +, on the other hand, have been reasonably well collected without yielding specimens of a + +Gephyrodesmus +species + +, and Coolah Tops (ca. +31º40'S +), the +type +locality for one of the new species described below, may be at or close to the northern range limit for the genus. In central +Victoria +, it is not yet known whether + +Gephyrodesmus + +occurs west of the Kilmore Gap, which separates the main, eastern mass of the Great Dividing Range from the smaller, scattered outliers of the Range to the west. + + +Remarks +: The four known + +Gephyrodesmus +species + +are very similar in size and general appearance, and differ chiefly in gonopod details and in the relative prominence of raised areas on the metatergites. In his genus description, +Jeekel (1983 +, p. 146) refers to 'Pleural keels weakly developed in a few anterior somites', but I could not confirm this observation in + +G. cineraceus + +or in the other three + +Gephyrodesmus +species + +; the pleural areas of the first rings are smoothly convex in anterior or posterior view. + + + + \ No newline at end of file diff --git a/data/38/2B/5C/382B5C2C97779C0AFF06FC88FECB0664.xml b/data/38/2B/5C/382B5C2C97779C0AFF06FC88FECB0664.xml new file mode 100644 index 00000000000..38aa17dcd73 --- /dev/null +++ b/data/38/2B/5C/382B5C2C97779C0AFF06FC88FECB0664.xml @@ -0,0 +1,256 @@ + + + +The millipede genera Gephyrodesmus Jeekel, 1983 and Orthorhachis Jeekel, 1985 in southeastern Australia, a new Lissodesmus Chamberlin, 1920 from Victoria, and observations on male leg setae, spinnerets and metatergite sculpture (Diplopoda: Polydesmida: Dalodesmidae) + + + +Author + +Mesibov, Robert + +text + + +Zootaxa + + +2008 + +2008-06-11 + + +1790 + + +1 +52 + + + +journal article +1175­5334 + + + + + + + +Gephyrodesmus arcuatus + +n. sp. + + + + + + +Figs. 6B +, +8 +; map +Fig. 12 + + + + +Holotype + +: +Male. Dyer Creek +, near +Murrungowar +, +Vic +, +37º38'26"S +148º43'24"E +, + +140 m + +, + +8 November 2006 + +, +R +. Mesibov & +T +. Moule. In +MV +, K-10633. + + + + + +Paratypes + +: +In +AM +: +2 males + +, + +Bondi State Forest +S of Bombala +, NSW, woodlot 1, +37º08'S +149º09'E +, + +27 September 1980 + +, +G. Gowing +et al +., litter, +KS11324 +; +2 males + +, + +Errinundra Road +, +2.5 km +from intersection with +Bonang Road +at entrance to +Errinundra National Park +, +Vic +, + +13 June 1999 + +, +A. Skates +, in log, +KS89499 + +. + + +In MV: + +1 male +, +Lind National Park +, +Vic +, 2 1/ +2 miles +from turnoff, ' +Grid +2331(1) +Map Ref +207364', no date or collector, 'rather dry open stringybark bloodwood forest bracken undergrowth', K-10630 + +; + +1 male +, +Slippery Hill +, N of +Dargo +, +Vic +, +37º23'05"S +147º12'54"E +, + +920 m + +, + +25 November 2004 + +, +R + +. + +Mesibov +& +T + +. + +Moule +, K- 10631 + +; +1 male +, details as for +holotype +, K-10632. + + +Other material examined +: None available. + + +Diagnosis +: Medial branch of gonopod telopodite large and arcuate, in lateral or medial view with squareedged tab on anterior surface near base and with tip bent anterobasally at ca. 90º; anterior edge of ring 7 aperture meeting anterior edge of prozonite; metatergite sculpture well-defined. + + +Description +: As for the genus. Male approximate measurements: length +18–19 mm +, midbody prozonite diameter 1.8–2.0 mm, midbody width across paranota 2.8–3.0 mm. In alcohol, well-coloured specimens fairly uniform light greyish-brown. Antennal sockets separated by ca. 2X a socket diameter. Collum as wide as head, narrower than tergite 2, D-shaped with posterior corners slightly produced. Raised areas on metatergites distinct ( +Fig. 6B +). Gonopod aperture about one-third width of prozonite, ovate rather than ovoid, longer than wide, anterior portion of aperture extended to meet anterior edge of prozonite, lateral edge raised posteriorly. + + +Gonopod telopodite ( +Fig. 8 +) with base wide, long setae on posterolateral surface to level of branching at about one-third telopodite height. Solenomere in two sections: basal half massive, mediolaterally flattened and with a slight posterior swelling; distal half much narrower, rounded, slightly tapering, arising at about two-thirds the telopodite length and directed first posteriorly, then abruptly distally, curving slightly posterolaterally. Medial branch large, somewhat flattened mediolaterally, C-shaped from base (concave posteriorly) with a prominent square-edged tab near base on anterolateral surface, then bending at nearly 90º posterobasally above basal section of solenomere and curving laterally to 'enclose' distal section of solenomere, finally bending anteromedially and slightly basally and terminating in a broad, rounded tip, with a pair of small, low, rounded bumps on the anterior surface of the terminal section. + +Female not yet recognised. + + +FIGURE 8. + +Gephyrodesmus arcuatus + + +n. sp. + +, male paratype, MV K-10632. (A) anterior, (B) lateral views of right gonopod telopodite. Setation not shown; dashed lines mark course of prostatic groove. Scale bar = 0.25 mm. + + + +Distribution +: Known from eucalypt forest at five localities from the lowlands to at least +920 m +in eastern +Victoria +and far southeastern +New South Wales +( +Fig. 12 +). Co-occurs with + +G. cineraceus + +near Murrungowar in East Gippsland. Found in moist leaf litter at the Dyer Creek and Slippery Creek sites. +Etymology +: Latin + +arcuatus + +, curved like a bow, adjective, for the shape of the medial telopodite branch. +Remarks +: The Slippery Creek male is pale and only +13 mm +long but conforms to the gonopod description given above. + + + + \ No newline at end of file diff --git a/data/38/2B/A2/382BA21F93547736FC3DC6B84EF98728.xml b/data/38/2B/A2/382BA21F93547736FC3DC6B84EF98728.xml new file mode 100644 index 00000000000..a8d46826176 --- /dev/null +++ b/data/38/2B/A2/382BA21F93547736FC3DC6B84EF98728.xml @@ -0,0 +1,86 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part H) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +557 +585 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Hesperis tristis +Linnaeus + +, + +Species Plantarum +2 + +: 663. 1753 + + +. + + + +"Habitat in Hungaria." RCN: 4828. + + + + +Lectotype +(Ball in Cafferty & Jarvis in +Taxon +51: 533. 2002): Herb. Linn. No. 841.1 ( +LINN +) + +. + + + + +Current name: + +Hesperis tristis +L. + +( +Brassicaceae +). + + + + \ No newline at end of file diff --git a/data/38/2C/05/382C05448222857A499AFBA127DE7595.xml b/data/38/2C/05/382C05448222857A499AFBA127DE7595.xml new file mode 100644 index 00000000000..a0756ac4cc4 --- /dev/null +++ b/data/38/2C/05/382C05448222857A499AFBA127DE7595.xml @@ -0,0 +1,154 @@ + + + +A new species of Tegenaria Latreille, 1804 (Araneae, Agelenidae) from Turkey + + + +Author + +Kaya, Rahsen S. + + + +Author + +Kunt, Kadir B. + + + +Author + +Marusik, Yuri M. + + + +Author + +Ugurtas, Ismail H. + +text + + +ZooKeys + + +2010 + +51 + + +1 +16 + + + + +http://dx.doi.org/10.3897/zookeys.51.467 + +journal article +http://dx.doi.org/10.3897/zookeys.51.467 +1313-2970-51-1 + + + + +23. +Tegenaria xenophontis Brignoli, 1978 +Fig. 20 + + + + +Tegenaria xenophontis +Brignoli 1978b +: 522, Figs 103, 105 (known from female only). + + + +General distribution: +Turkey. + + +Distribution in Turkey: + +Trabzon Province: +Macka +District ( +Suemela +Monastery) and Zigana Pass ( +Brignoli 1978b +). + + + +Figure +17 The distribution of +Tegenaria agrestis +(? = no exact locality in Anatolia; see +Caporiacco, 1935 +), +Tegenaria domestica +(1) and +Tegenaria parietina +(2) in Turkey. + + + + +Figure 18 The distribution of +Tegenaria atrica +(1) in Turkey. + + + + +Figure 19 The distribution of +Tegenaria bithyniae +(1), +Tegenaria longimana +(2) and +Tegenaria rhodiensis +(3) in Turkey. + + + + +Figure 20 The distribution of +Tegenaria agnolettii +(1), +Tegenaria averni +(2), +Tegenaria comnena +(3), +Tegenaria cottarellii +(4), +Tegenaria elysii +(5), +Tegenaria faniapollinis +(6), +Tegenaria forestieroi +(7), +Tegenaria hamid +(8), +Tegenaria karaman +(9), +Tegenaria mamikonian +(10), +Tegenaria melbae +(11), +Tegenaria percuriosa +(12), +Tegenaria tekke +(13), +Tegenaria vignai +(14), +Tegenaria xenophontis +(15) and +Tegenaria bayrami sp +. n. (star) in Turkey. + + + + + \ No newline at end of file diff --git a/data/38/2C/4F/382C4F214C4D5D4F801E642E5B814422.xml b/data/38/2C/4F/382C4F214C4D5D4F801E642E5B814422.xml new file mode 100644 index 00000000000..35640c4822e --- /dev/null +++ b/data/38/2C/4F/382C4F214C4D5D4F801E642E5B814422.xml @@ -0,0 +1,319 @@ + + + +The genus Diplocheila Brulle, 1834 in Cambodia, with descriptions of two new species (Coleoptera, Carabidae, Licinini) + + + +Author + +Allegro, Gianni +https://orcid.org/0000-0002-5079-6671 +Strada Patro 11, I- 14036 Moncalvo (AT), Italy +gianni.allegro54@gmail.com + + + +Author + +Giachino, Pier Mauro +https://orcid.org/0000-0002-1167-5447 +Via della Trinita 13, I- 10010 San Martino Canavese (TO), Italy + +text + + +ZooKeys + + +2021 + +2021-06-16 + + +1044 + + +427 +448 + + + + +http://dx.doi.org/10.3897/zookeys.1044.60072 + +journal article +http://dx.doi.org/10.3897/zookeys.1044.60072 +1313-2970-1044-427 +9AA72654B6CC4081B557CD0BAE3939A3 +8320077CEFA5571D971EFEA66B0C6268 + + + + +Diplocheila (Diplocheila) laevigata (Bates, 1892) +Figures 2 +, 6 +, 8 +, 12 +, 14 +, 18 +, 20 +, 26 +, 27 + + + + +Rembus politus +MacLeay 1825 +: 16 + + +Rembus politus +MacLeay, 1825: +Redtenbacher 1867 +: 10 + + +Rhembus laevigatus +Bates 1892 +: 326 + + +Eccoptogenius moestus +Bates 1889 +: 267 + + +Eccoptogenius moestus +Bates, 1889: +Andrewes 1921 +: 176 + + +Diplochila laevigata +(Bates, 1892): +Andrewes 1921 +: 177 + + +Diplochila laevigata +(Bates, 1892): +Andrewes 1922 +: 282 + + +Diplocheila laevigata +(Bates, 1892): +Andrewes 1930 +: 149 + + +Diplocheila laevigata +(Bates, 1892): +Habu 1956 +: 55 + + +Diplocheila laevigata +(Bates, 1892): +Ball 1959 +: 35 + + +Diplocheila laevigata +(Bates, 1892): +Lorenz 2005a +: 342 + + +Diplocheila laevigata +(Bates, 1892): +Lorenz 2005b +: 571 + + +Diplocheila laevigata +(Bates, 1892): +Lafer and Kataev 2008 +: 682 + + +Diplocheila laevigata +(Bates, 1892): +Huber and Marggi 2017 +: 626 + + + +Type locality. +Kawkareet in Tenasserim (Myanmar). + + +Material examined. + +Myanmar +: HT + + +, +Kawkareet in Tenasserim +, +Gen. Febbr. +1887, +Fea +legit (MCSNG) (figs 2, 6, 12, 26) + +. + +Cambodia +: +3 ♂♂ +2 ♀♀ +Kampong Chhnang +, banks of +Tonle Sap Lake +, +17.V.2019 +, +W. Rossi +and +V. Kong +leg. (CAl, CGi) + +; + +1 ♂ +Kampong Chhnang +, +Rolea +B'ier +District +, +Toekchenh Village +, +18.V.2019 +, +W. Rossi +and +V. Kong +leg. (CAl) + +; + +1 ♂ +, +Khsam +, +Kampong Chhnang +, +12°16'47"N +, +104°39'28.6"E +, +29.XI-3.XII.2019 +, +light trap +, +W. Rossi +and +V. Kong +leg. (CAl) + +. + + + +Figure 2. + +Diplocheila laevigata + +(Bates, 1892): habitus of +holotype +. + + + + +Diagnosis. + + +Diplocheila laevigata + +may be distinguished by the combination of the following characters. ABL = 14-16 mm; head with 1 supraorbital setiferous pore on each side; labrum with 6 setae (4 medial + 2 lateral), symmetrical and moderately emarginate (LR = 0.63-0.65) (Figs +12 +, +14 +); anterior margin of clypeus hardly concave (Fig. +12 +); pronotum transverse (PW/PL = 1.29-1.31), with sides delicately sinuate backwards (Fig. +6 +); elytral striae distinctly punctate; apical lamella of the median lobe of aedeagus in dorsal view shortly triangular, with blunt apex (Figs +20 +, +26 +). + + + +Remarks. + + +Diplocheila laevigata + +is recorded from southern China, Myanmar, Vietnam, Laos, and Cambodia ( +Andrewes 1922 +; +Ball 1959 +; +Lafer and Kataev 2008 +). Unfortunately, the male HT in the Fea Collection at MCSNG is an immature specimen (Fig. +2 +) with a scarcely chitinized aedeagus (Fig. +26 +); however, its examination, made possible thanks to the courtesy of the Honorary Curator Roberto Poggi, revealed that it was conspecific with the specimens from Cambodia (Figs +8 +, +14 +, +27 +). An aedeagus of + +D. laevigata + +, substantially corresponding to the HT, is also illustrated by +Lafer and Kataev (2008) +. + + +Two specimens from Thailand deposited in CGi (2 ♂♂, Chiang Mai, 6.V.1988, R. Sciaky det.; Figs +9 +, +15 +) show a similar aedeagal morphology but pronotum and labrum are differently shaped compared to the HT and to the specimens from Cambodia; they could belong to a new species, but it is not described here, awaiting more abundant material. A further specimen from Thailand deposited at BMNH (1 ♀, Bangkok, Larnaudie leg., H.E. Andrewes Coll.) probably belongs to a different, new species. + + +A male specimen from Indonesia deposited at BMNH (1 ♂, Indes Neerl., Boucard leg., H.E. Andrewes Coll.) differs from the + +D. laevigata + +HT not only in external morphology, but also in the shape of the aedeagus (although this is damaged, the apical lamella appears to be clearly different); its external morphology does not match + +D. laevigotoides + +HT either, in spite of the opinion of +Lafer and Kataev (2008) +that the records of + +D. laevigata + +from Indonesia, together with those from Japan and the Philippines, are probably instead + +D. laevigotoides + +. Therefore, this specimen also likely belongs to a new species, awaiting description when more abundant material becomes available. + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF2FFE9FF63FA13FE65F9CB.xml b/data/38/2D/12/382D1232FFF2FFE9FF63FA13FE65F9CB.xml new file mode 100644 index 00000000000..e0c865c86ec --- /dev/null +++ b/data/38/2D/12/382D1232FFF2FFE9FF63FA13FE65F9CB.xml @@ -0,0 +1,88 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 + + + + + + + +Clistoabdoominalis sinaiensis +(De Meyer, 1995) + + + + + + + +DISTRIBUTION. +Iran +: +Fars +, Lar, Darab (Majnon Jahromi +et al +., 2017). – Sinai Peninsula + +(Kehlmaier, 2005b). + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF2FFE9FF63FB53FCB8FB07.xml b/data/38/2D/12/382D1232FFF2FFE9FF63FB53FCB8FB07.xml new file mode 100644 index 00000000000..8531d44d4ff --- /dev/null +++ b/data/38/2D/12/382D1232FFF2FFE9FF63FB53FCB8FB07.xml @@ -0,0 +1,94 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Clistoabdominalis nitidifrons +(Becker, 1900) + + + + + + + +DISTRIBUTION. +Iran +: +Kermanshah +, Sar pol zahab (Motamedinia +et al +., 2017c). – + + +Palaearctic and +Oriental +regions (Kehlmaier, 2005b; Földvári, 2013). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF2FFE9FF63FBA4FB90FB76.xml b/data/38/2D/12/382D1232FFF2FFE9FF63FBA4FB90FB76.xml new file mode 100644 index 00000000000..5f41eaa2bbf --- /dev/null +++ b/data/38/2D/12/382D1232FFF2FFE9FF63FBA4FB90FB76.xml @@ -0,0 +1,85 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 + + + + + + + +Clistoabdominalis hyrcania +Kazerani et Kehlmaier, 2018 + + + + + + + +DISTRIBUTION. Endemic to +Iran +: +Golestan +, Shast-Kola (Kazerani & Kehlmaier, 2018). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF2FFE9FF63FC4FFB9BFC01.xml b/data/38/2D/12/382D1232FFF2FFE9FF63FC4FFB9BFC01.xml new file mode 100644 index 00000000000..c9ebc06acb7 --- /dev/null +++ b/data/38/2D/12/382D1232FFF2FFE9FF63FC4FFB9BFC01.xml @@ -0,0 +1,89 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Claraeola khorshidae +Motamedinia et Kehlmaier, 2017 + + + + + + + +DISTRIBUTION. Endemic to +Iran +: +South Khorasan +, Birjand (Motamedinia +et al +., 2017a). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF2FFE9FF63FCCBFEEFFC62.xml b/data/38/2D/12/382D1232FFF2FFE9FF63FCCBFEEFFC62.xml new file mode 100644 index 00000000000..eca72c99a8d --- /dev/null +++ b/data/38/2D/12/382D1232FFF2FFE9FF63FCCBFEEFFC62.xml @@ -0,0 +1,88 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Claraeola parnianae +Motamedinia et Kehlmaier, 2017 + + + + + + + +DISTRIBUTION. Endemic to +Iran +: Sistan and Baluchestan, Zabol (Motamedinia +et al +., + +2017a). + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF2FFE9FF63FD36FC4CFCE8.xml b/data/38/2D/12/382D1232FFF2FFE9FF63FD36FC4CFCE8.xml new file mode 100644 index 00000000000..dfc179601dd --- /dev/null +++ b/data/38/2D/12/382D1232FFF2FFE9FF63FD36FC4CFCE8.xml @@ -0,0 +1,95 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Claraeola conjuncta +(Collin, 1949) + + + + + + + +DISTRIBUTION. +Iran +: Sistan and Baluchestan, Zabol. +South Khorasan +, Birjand (Motamedinia +et al +., 2017c). – +Algeria +, +Egypt +and +Israel +(Kehlmaier, 2005b). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF2FFE9FF63FE22FD3AFD9C.xml b/data/38/2D/12/382D1232FFF2FFE9FF63FE22FD3AFD9C.xml new file mode 100644 index 00000000000..c88d10a8cd2 --- /dev/null +++ b/data/38/2D/12/382D1232FFF2FFE9FF63FE22FD3AFD9C.xml @@ -0,0 +1,109 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Cephalops ultimus +(Becker, 1900) + + + + + + + + +DISTRIBUTION. +Iran +: +Alborz + +, + +Kordan ( +Kehlmaier +& +Majnon Jahromi +, 2015), +Fars + +, + + +Jahrom (Majnon Jahromi +et al +., 2017). – West Palaearctic. + + + +Tribe +Eudorylini + + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF2FFE9FF63FE8DFC28FE40.xml b/data/38/2D/12/382D1232FFF2FFE9FF63FE8DFC28FE40.xml new file mode 100644 index 00000000000..d942733dafa --- /dev/null +++ b/data/38/2D/12/382D1232FFF2FFE9FF63FE8DFC28FE40.xml @@ -0,0 +1,93 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Cephalops +( +Semicephalops +) +penultimus +Ackland, 1993 + + + + + + + +DISTRIBUTION. +Iran +: +Kurdistan +, Saghez (Kazerani +et al +., 2017). – Europe. + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF3FFE8FF63FB1DFD3EFA50.xml b/data/38/2D/12/382D1232FFF3FFE8FF63FB1DFD3EFA50.xml new file mode 100644 index 00000000000..18321bc8c8f --- /dev/null +++ b/data/38/2D/12/382D1232FFF3FFE8FF63FB1DFD3EFA50.xml @@ -0,0 +1,102 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 + + + + + + + +Nephrocercus scutellatus +(Macquart, 1834) + + + + + + + +DISTRIBUTION. +Iran +: +East Azerbaijan +, Arasbaran (Kazerani +et al +., 2017). – West + +Palaearctic (Kehlmaier & Floren, 2010). + + +Subfamily +Pipunculinae + + + + + + +Tribe +Pipunculini + + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF3FFE8FF63FBFEFCE7FB64.xml b/data/38/2D/12/382D1232FFF3FFE8FF63FBFEFCE7FB64.xml new file mode 100644 index 00000000000..552de7fbc01 --- /dev/null +++ b/data/38/2D/12/382D1232FFF3FFE8FF63FBFEFCE7FB64.xml @@ -0,0 +1,101 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Verrallia aucta +(Fallén, 1817) + + + + + + + +DISTRIBUTION. +Iran +: +East Azerbaijan +, Arasbaran (Kazerani +et al +., 2017). – +Israel +, + + +Kazakhstan +(De Meyer, 1996). + + + +Subfamily +Nephrocerinae + + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF3FFE8FF63FC93FEF2FC46.xml b/data/38/2D/12/382D1232FFF3FFE8FF63FC93FEF2FC46.xml new file mode 100644 index 00000000000..4d6375660c5 --- /dev/null +++ b/data/38/2D/12/382D1232FFF3FFE8FF63FC93FEF2FC46.xml @@ -0,0 +1,88 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Chalarus indistinctus +Jervis, 1992 + + + + + + + +DISTRIBUTION. +Iran +: +Alborz +, Kordan (Kehlmaier & Majnon Jahromi, 2015). – + +Europe. + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF3FFE8FF63FD02FC79FCB0.xml b/data/38/2D/12/382D1232FFF3FFE8FF63FD02FC79FCB0.xml new file mode 100644 index 00000000000..0ec59afaafb --- /dev/null +++ b/data/38/2D/12/382D1232FFF3FFE8FF63FD02FC79FCB0.xml @@ -0,0 +1,94 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Chalarus brevicaudis +Jervis, 1992 + + + + + + + +DISTRIBUTION. +Iran +: +Alborz +, Kordan (Kehlmaier & Majnon Jahromi, 2015); +East + + +Azerbaijan +, Kandovan (Kazerani +et al +., 2017). – Europe (Kehlmaier, 2011). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF3FFE9FF63FA09FCC6FEE9.xml b/data/38/2D/12/382D1232FFF3FFE9FF63FA09FCC6FEE9.xml new file mode 100644 index 00000000000..59d6936e118 --- /dev/null +++ b/data/38/2D/12/382D1232FFF3FFE9FF63FA09FCC6FEE9.xml @@ -0,0 +1,97 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Pipunculus lenis +Kuznetzov, 1991 + + + + + + + +DISTRIBUTION. +Iran +: +Lorestan +, Khorramabad (Kazerani +et al +., 2017). – +Russia +(European part). + + + +Tribe +Cephalopsini + + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF4FFEFFF63FA6DFBE1F9CD.xml b/data/38/2D/12/382D1232FFF4FFEFFF63FA6DFBE1F9CD.xml new file mode 100644 index 00000000000..e6f7a50f3f9 --- /dev/null +++ b/data/38/2D/12/382D1232FFF4FFEFFF63FA6DFBE1F9CD.xml @@ -0,0 +1,139 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella coquilletti +(Kertész, 1907) + + + + + + + + +MATERIAL EXAMINED. +Iran +: +Fars +, +Jahrom +, +28°30′N +53°35′E +, + +1044 m + +, +window trap + +, + + +10–28.IX 2016 +, +2♂ +, leg. B. Majnon Jahromi. + + + + + +DISTRIBUTION. +Iran +: +Ilam +, +Dalab forest +park (Gharali +et al +., 2008), +Alborz +, Kordan + + + +(Kehlmaier & Majnon Jahromi, 2015), +Ardabil +, Meshgin Shahr (Kazerani +et al +., 2017), +Fars +, + + +Kherameh (Majnon Jahromi +et al +., 2017). – Nearctic, Palaearctic and +Oriental +regions. + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF4FFEFFF63FB04FBE5FA82.xml b/data/38/2D/12/382D1232FFF4FFEFFF63FB04FBE5FA82.xml new file mode 100644 index 00000000000..61c56f9cc0f --- /dev/null +++ b/data/38/2D/12/382D1232FFF4FFEFFF63FB04FBE5FA82.xml @@ -0,0 +1,107 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella +cf +brachybasis +De Meyer, 1993 + + + + + + + +DISTRIBUTION. +Iran +: +Alborz +, Kordan, Arangeh (Kehlmaier & Majnon Jahromi, + +2015). + +NOTES. True + +T. brachybasis + +have been recorded from +South Africa +( +Botswana +, + + +Namibia +, and +South Africa +) and Canary Islands (Kehlmaier & Majnon Jahromi, 2015). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF4FFEFFF63FB68FBF2FB3B.xml b/data/38/2D/12/382D1232FFF4FFEFFF63FB68FBF2FB3B.xml new file mode 100644 index 00000000000..deedfcea3d1 --- /dev/null +++ b/data/38/2D/12/382D1232FFF4FFEFFF63FB68FBF2FB3B.xml @@ -0,0 +1,91 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella argyrata +De Meyer, 1995 + + + + + + + +DISTRIBUTION. +Iran +: +East Azerbaijan +, Arasbaran (Kazerani +et al +., 2017). – +Israel +. + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF4FFEFFF63FBBFFBF9FB8F.xml b/data/38/2D/12/382D1232FFF4FFEFFF63FBBFFBF9FB8F.xml new file mode 100644 index 00000000000..e00f84a9993 --- /dev/null +++ b/data/38/2D/12/382D1232FFF4FFEFFF63FBBFFBF9FB8F.xml @@ -0,0 +1,89 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella angulata +Kehlmaier et Majnon Jahromi, 2017 + + + + + + + +DISTRIBUTION. Endemic to +Iran +: +Fars +, Jahrom, Lar (Majnon Jahromi +et al +., 2017). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF4FFEFFF63FC56FEBDFC04.xml b/data/38/2D/12/382D1232FFF4FFEFFF63FC56FEBDFC04.xml new file mode 100644 index 00000000000..92f3293b254 --- /dev/null +++ b/data/38/2D/12/382D1232FFF4FFEFFF63FC56FEBDFC04.xml @@ -0,0 +1,97 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Dorylomorpha +( +Dorylomya +) +tanasijtshuki +Albrecht, 1990 + + + + + + + +DISTRIBUTION. +Iran +: +East Azerbaijan +, Sufian (Kazerani +et al +., 2017). – +Kyrgyzstan +and +Uzbekistan +. + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF4FFEFFF63FD79FCD6FCBE.xml b/data/38/2D/12/382D1232FFF4FFEFFF63FD79FCD6FCBE.xml new file mode 100644 index 00000000000..ab02e1c966b --- /dev/null +++ b/data/38/2D/12/382D1232FFF4FFEFFF63FD79FCD6FCBE.xml @@ -0,0 +1,113 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Eudorylas zermattensis +(Becker, 1897) + + + + + + + +DISTRIBUTION. +Iran +: +Alborz +, Kordan, Arangeh (Kehlmaier & Majnon Jahromi, + + +2015), +Kurdistan +, Saghez and +East Azerbaijan +, Arasbaran (Kazerani +et al +., 2017), +Fars +, + + +Kazeroon (Majnon Jahromi +et al +., 2017), +Kermanshah +, Gheshlagh (Motamedinia +et al., + +2017d). – West Palaearctic. + + +Tribe +Tomosvaryellini + + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF4FFEFFF63FDE8FD4FFD9F.xml b/data/38/2D/12/382D1232FFF4FFEFFF63FDE8FD4FFD9F.xml new file mode 100644 index 00000000000..53290a93e86 --- /dev/null +++ b/data/38/2D/12/382D1232FFF4FFEFFF63FDE8FD4FFD9F.xml @@ -0,0 +1,102 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Eudorylas pannonicus +(Becker, 1897) + + + + + + + + +DISTRIBUTION. +Iran +: +Ilam + +, + +Dalab forest +park (Gharali +et al +., 2008), +West Azerbaijan + +, + + +Urmia (Kazerani +et al +., 2017). – Palaearctic. + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF4FFEFFF63FE83FEEFFE0F.xml b/data/38/2D/12/382D1232FFF4FFEFFF63FE83FEEFFE0F.xml new file mode 100644 index 00000000000..5be99d92318 --- /dev/null +++ b/data/38/2D/12/382D1232FFF4FFEFFF63FE83FEEFFE0F.xml @@ -0,0 +1,107 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Eudorylas longifrons +Coe, 1966 + + + + + + + +DISTRIBUTION. +Iran +: +Alborz +, Kordan (Kehlmaier & Majnon Jahromi, 2015), +East + + +Azerbaijan +, Arasbaran (Kazerani +et al +., 2017), Fars, Jahrom (Majnon Jahromi +et al +., 2017), + + + +North Khorasan +, Bojnord (Motamedinia +et al., +2017c). – +West Palaearctic +(Kehlmaier, + + +2005a). + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF4FFEFFF63FEF2FDD7FEA0.xml b/data/38/2D/12/382D1232FFF4FFEFFF63FEF2FDD7FEA0.xml new file mode 100644 index 00000000000..cf50e7fa391 --- /dev/null +++ b/data/38/2D/12/382D1232FFF4FFEFFF63FEF2FDD7FEA0.xml @@ -0,0 +1,90 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Eudorylas jenkinsoni +Coe, 1966 + + + + + + + +DISTRIBUTION. +Iran +: +Kermanshah +, Sar pol zahab (Motamedinia +et al., +2017c). – East + +Palaearctic (Kehlmaier, 2005a). + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF5FFEEFF63FA30FD61F9DA.xml b/data/38/2D/12/382D1232FFF5FFEEFF63FA30FD61F9DA.xml new file mode 100644 index 00000000000..4e37478769c --- /dev/null +++ b/data/38/2D/12/382D1232FFF5FFEEFF63FA30FD61F9DA.xml @@ -0,0 +1,118 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Eudorylas fluviatilis +(Becker, 1900) + + + + + + + +DISTRIBUTION. + +Iran +: +Fars +, +Jahrom +(Majnon Jahromi +et al +., 2017) + +, + +Kermanshah +, +Sar +pol zahab + +; + +North Khorasan +, +Bojnord + +; + +South Khorasan +, +Birjand +( +Motamedinia +et al., +2017c) + +. + +– Near East, North Africa (Kehlmaier, 2005a). + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF5FFEEFF63FAA2FEADFA50.xml b/data/38/2D/12/382D1232FFF5FFEEFF63FAA2FEADFA50.xml new file mode 100644 index 00000000000..5d48e3d5e4c --- /dev/null +++ b/data/38/2D/12/382D1232FFF5FFEEFF63FAA2FEADFA50.xml @@ -0,0 +1,89 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Eudorylas fascipes +(Zetterstedt, 1844) + + + + + + + +DISTRIBUTION. +Iran +: +West Azerbaijan +, Khoy (Kazerani +et al +., 2017). – Europe (Kehlmaier, 2005a). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF5FFEEFF63FB1DFC4CFAC1.xml b/data/38/2D/12/382D1232FFF5FFEEFF63FB1DFC4CFAC1.xml new file mode 100644 index 00000000000..2fa5aa9b46d --- /dev/null +++ b/data/38/2D/12/382D1232FFF5FFEEFF63FB1DFC4CFAC1.xml @@ -0,0 +1,98 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Eudorylas chvalai +Kozánek, 1988 + + + + + + + + +DISTRIBUTION. +Iran +: +Fars + +, Kazeroon (Majnon Jahromi +et al +., 2017), +South Khorasan +, + + +Birjand (Motamedinia +et al., +2017c). – Palaearctic (Kehlmaier, 2005a). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF5FFEEFF63FBD2FDD7FB33.xml b/data/38/2D/12/382D1232FFF5FFEEFF63FBD2FDD7FB33.xml new file mode 100644 index 00000000000..2b7bea6406d --- /dev/null +++ b/data/38/2D/12/382D1232FFF5FFEEFF63FBD2FDD7FB33.xml @@ -0,0 +1,114 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Eudorylas blascoi +De Meyer, 1997 + + + + + + + +DISTRIBUTION. +Iran +: +Alborz +, Kordan, Arangeh (Kehlmaier & Majnon Jahromi, + + +2015), +East Azerbaijan +, Sufian (Kazerani +et al +., 2017), +Fars +, Jahrom, Darab (Majnon + + +Jahromi +et al +., 2017), +Kermanshah +, Sar pol zahab; +Khorasan +Razavi, Mashhad, Torqabeh; + + +North Khorasan +, Bojnord; +South Khorasan +, Birjand; (Motamedinia +et al., +2017c). – + +Palaearctic (Kehlmaier, 2005a). + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF5FFEEFF63FC4CFD46FBF2.xml b/data/38/2D/12/382D1232FFF5FFEEFF63FC4CFD46FBF2.xml new file mode 100644 index 00000000000..ef2910976ed --- /dev/null +++ b/data/38/2D/12/382D1232FFF5FFEEFF63FC4CFD46FBF2.xml @@ -0,0 +1,97 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Eudorylas auctus +Kehlmaier, 2005 + + + + + + + +DISTRIBUTION. +Iran +: +Kurdistan +, Saghez (Kazerani +et al +., 2017). – +Kyrgyzstan +, + + +Tajikistan +, +Uzbekistan +(Kehlmaier, 2005a). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF5FFEEFF63FCDAFB86FC94.xml b/data/38/2D/12/382D1232FFF5FFEEFF63FCDAFB86FC94.xml new file mode 100644 index 00000000000..9cea1b630ca --- /dev/null +++ b/data/38/2D/12/382D1232FFF5FFEEFF63FCDAFB86FC94.xml @@ -0,0 +1,89 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Dasydorylas zardouei +Motamedinia & Kehlmaier, 2017 + + + + + + + +DISTRIBUTION. Endemic to +Iran +: +Kermanshah +, Dodan (Motamedinia +et al., +2017b). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF5FFEEFF63FD35FDD7FCF9.xml b/data/38/2D/12/382D1232FFF5FFEEFF63FD35FDD7FCF9.xml new file mode 100644 index 00000000000..d72c81d7161 --- /dev/null +++ b/data/38/2D/12/382D1232FFF5FFEEFF63FD35FDD7FCF9.xml @@ -0,0 +1,88 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Dasydorylas horridus +(Becker, 1897) + + + + + + + +DISTRIBUTION. +Iran +: +Alborz +, Kordan (Kehlmaier & Majnon Jahromi, 2015). – West + +Palaearctic (Kehlmaier, 2005a). + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF5FFEEFF63FDA7FE2EFD6B.xml b/data/38/2D/12/382D1232FFF5FFEEFF63FDA7FE2EFD6B.xml new file mode 100644 index 00000000000..5ca30baa4d1 --- /dev/null +++ b/data/38/2D/12/382D1232FFF5FFEEFF63FDA7FE2EFD6B.xml @@ -0,0 +1,91 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Dasydorylas discoidalis +(Becker, 1897) + + + + + + + +DISTRIBUTION. +Iran +: Sistan and Baluchestan, Zabol (Motamedinia +et al., +2017c). – + + +Russia +(Kehlmaier, 2005a). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF5FFEEFF63FEF2FE12FE7F.xml b/data/38/2D/12/382D1232FFF5FFEEFF63FEF2FE12FE7F.xml new file mode 100644 index 00000000000..5a8d6fb144c --- /dev/null +++ b/data/38/2D/12/382D1232FFF5FFEEFF63FEF2FE12FE7F.xml @@ -0,0 +1,113 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 + + + + + + + +Clistoabdoominalis trochanteratus +(Becker, 1900) + + + + + + + + +DISTRIBUTION. +Iran +: +Alborz + +, + +Kordan ( +Kehlmaier +& +Majnon Jahromi +, 2015), +Fars + +, + + +Jahrom (Majnon Jahromi +et al +., 2017), +Kermanshah +, Sar pol zahab; Sistan and Baluchestan, + + +Zabol; South Khorasan, Birjand (Motamedinia +et al +., 2017c). – +Egypt +(Skevington +et al +., + +2007; Kehlmaier, 2005). + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF5FFEEFF6AFE11FEECFDC5.xml b/data/38/2D/12/382D1232FFF5FFEEFF6AFE11FEECFDC5.xml new file mode 100644 index 00000000000..3a60a7d5663 --- /dev/null +++ b/data/38/2D/12/382D1232FFF5FFEEFF6AFE11FEECFDC5.xml @@ -0,0 +1,87 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Dasydorylas derafshani +Motamedinia et Kehlmaier, 2017 + + + + + + + +DISTRIBUTION. Endemic to +Iran +: Sistan and Baluchestan, Zabol (Motamedinia +et al., + +2017b). + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF6FFEDFF63FA14FEE0F9BD.xml b/data/38/2D/12/382D1232FFF6FFEDFF63FA14FEE0F9BD.xml new file mode 100644 index 00000000000..622119afcb8 --- /dev/null +++ b/data/38/2D/12/382D1232FFF6FFEDFF63FA14FEE0F9BD.xml @@ -0,0 +1,108 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella sylvatica +(Meigen, 1824) + + + + + + + + +DISTRIBUTION. +Iran +: +Lorestan +, Khorramabad (Kazerani +et al +., 2017), +Fars +, Neyriz + + + +(Majnon Jahromi +et al +., 2017). – + +Nearctic, Palaearctic, +Oriental +( +Foldvary +& +De Meyer +, + + +1999). + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF6FFEDFF63FAD5FC63FA4B.xml b/data/38/2D/12/382D1232FFF6FFEDFF63FAD5FC63FA4B.xml new file mode 100644 index 00000000000..3b1c9d04c67 --- /dev/null +++ b/data/38/2D/12/382D1232FFF6FFEDFF63FAD5FC63FA4B.xml @@ -0,0 +1,129 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella subvirescens +(Loew, 1872) + + + + + + + + +MATERIAL EXAMINED. +Iran +: +Fars +, +Jahrom +, +28°30′N +53°35′E +, + +1044 m + +, +window trap + +, + + +10–28 IX.2016 +, +1♂ +, leg. B. Majnon Jahromi. + + + + +DISTRIBUTION. +Iran +: +Alborz +, Arangeh, Kordan (Kehlmaier & Majnon Jahromi, 2015) + + +– +Egypt +, +Israel +, +Yemen +(De Meyer, 1993, 1995). + + +NOTE. This species is recorded from +Fars province +for the first time. + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF6FFEDFF63FB38FBFDFB09.xml b/data/38/2D/12/382D1232FFF6FFEDFF63FB38FBFDFB09.xml new file mode 100644 index 00000000000..cc8f98b4503 --- /dev/null +++ b/data/38/2D/12/382D1232FFF6FFEDFF63FB38FBFDFB09.xml @@ -0,0 +1,87 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 + + + + + + + +Tomosvaryella subsylvatica +Kehlmaier et Kazerani, 2017 + + + + + + + +DISTRIBUTION. Endemic to +Iran +: +East Azerbaijan +, Qurigol, (Kazerani +et al +., 2017). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF6FFEDFF63FBABFD64FB5F.xml b/data/38/2D/12/382D1232FFF6FFEDFF63FBABFD64FB5F.xml new file mode 100644 index 00000000000..ad5cad317de --- /dev/null +++ b/data/38/2D/12/382D1232FFF6FFEDFF63FBABFD64FB5F.xml @@ -0,0 +1,88 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella propinqua +(Becker, 1913) + + + + + + + +DISTRIBUTION. Endemic to +Iran +: Sistan and Baluchestan (Becker, 1913), +Alborz +, + +Kordan (Kehlmaier & Majnon Jahromi, 2015). + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF6FFEDFF63FBF9FBE8FBC8.xml b/data/38/2D/12/382D1232FFF6FFEDFF63FBF9FBE8FBC8.xml new file mode 100644 index 00000000000..823b873b54d --- /dev/null +++ b/data/38/2D/12/382D1232FFF6FFEDFF63FBF9FBE8FBC8.xml @@ -0,0 +1,89 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella pistacia +Majnon Jahromi et Kehlmaier, 2017 + + + + + + + +DISTRIBUTION. Endemic to +Iran +: +Fars +, Kherameh (Majnon Jahromi +et al +., 2017). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF6FFEDFF63FCBFFC6DFC1E.xml b/data/38/2D/12/382D1232FFF6FFEDFF63FCBFFC6DFC1E.xml new file mode 100644 index 00000000000..8aa355eabf0 --- /dev/null +++ b/data/38/2D/12/382D1232FFF6FFEDFF63FCBFFC6DFC1E.xml @@ -0,0 +1,124 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella parakuthyi +De Meyer, 1995 + + + + + + + + +MATERIAL EXAMINED. +Iran +: +Fars +, +Jahrom +, +28°30′N +53°35′E +, + +1044 m + +, +window trap + +, + + +10–28 IX.2016 +, +3♂ +, leg. B. Majnon Jahromi. + + + + +DISTRIBUTION. +Iran +: +Alborz +, Arangeh (Kehlmaier & Majnon Jahromi, 2015), +East + + +Azerbaijan +, Shabestar (Kazerani +et al +., 2017), Fars, Jahrom, Lar, Marvdasht (Majnon Jahromi +et al +., 2017). – Canary Is, Near East, North Africa (De Meyer, 1995). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF6FFEDFF63FD29FDF8FCDD.xml b/data/38/2D/12/382D1232FFF6FFEDFF63FD29FDF8FCDD.xml new file mode 100644 index 00000000000..8e7ab4f65b5 --- /dev/null +++ b/data/38/2D/12/382D1232FFF6FFEDFF63FD29FDF8FCDD.xml @@ -0,0 +1,95 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella nodosa +De Meyer, 1993 + + + + + + + +DISTRIBUTION. +Iran +: +Fars +, Jahrom, Lar, Marvdasht (Majnon Jahromi +et al +., 2017). – + + +Egypt +and +Israel +(De Meyer, 1995). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF6FFEDFF63FDC3FD1FFD4E.xml b/data/38/2D/12/382D1232FFF6FFEDFF63FDC3FD1FFD4E.xml new file mode 100644 index 00000000000..07b25021363 --- /dev/null +++ b/data/38/2D/12/382D1232FFF6FFEDFF63FDC3FD1FFD4E.xml @@ -0,0 +1,123 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella minuscula +(Collin, 1956) + + + + + + + + +MATERIAL EXAMINED. +Iran +: +Fars +, +Jahrom +, +28°30′31″N +53°34′21″E +, + +1044 m + +, +window trap +, + +8–18.X 2016 + +, +1♂ +, leg. +B. Majnon Jahromi. + + + + + +DISTRIBUTION. +Iran +: +Fars +(new record). – +Egypt +(Foldvary & De Meyer, 1999). + + +NOTE. This species is new for the fauna of +Iran +. + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF6FFEDFF63FE64FBCDFDE0.xml b/data/38/2D/12/382D1232FFF6FFEDFF63FE64FBCDFDE0.xml new file mode 100644 index 00000000000..ad85a9d3358 --- /dev/null +++ b/data/38/2D/12/382D1232FFF6FFEDFF63FE64FBCDFDE0.xml @@ -0,0 +1,131 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella minima +(Becker, 1897) + + + + + + + + +MATERIAL EXAMINED. +Iran +: +Fars +, +Jahrom +, +28°30′N +53°35′E +, + +1044 m + +, +window trap + +, + + +10–28 IX.2016 +, +1♂ +, leg. B. Majnon Jahromi. + + + + + +DISTRIBUTION. +Iran +: +Alborz + +, + +Kordan ( +Kehlmaier +& +Majnon Jahromi +, 2015), +Fars + +, + + +Jahrom, Lar (Majnon Jahromi +et al +., 2017). – Europe (Foldvary & De Meyer, 1999). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF6FFEDFF63FEF2FE4CFE9B.xml b/data/38/2D/12/382D1232FFF6FFEDFF63FEF2FE4CFE9B.xml new file mode 100644 index 00000000000..e59e1239704 --- /dev/null +++ b/data/38/2D/12/382D1232FFF6FFEDFF63FEF2FE4CFE9B.xml @@ -0,0 +1,102 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella kuthyi +Aczél, 1994 + + + + + + + + +DISTRIBUTION. +Iran +: +Ilam +, +Dalab forest +park (Gharali +et al +., 2008), +Fars +, Jahrom, Lar + +, + + +Kherameh, Sepidan (Majnon Jahromi +et al +., 2017). – West and Central Europe (Foldvary & + +De Meyer, 1999). + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF7FFECFF63FA53FC84F9D9.xml b/data/38/2D/12/382D1232FFF7FFECFF63FA53FC84F9D9.xml new file mode 100644 index 00000000000..ba012df193e --- /dev/null +++ b/data/38/2D/12/382D1232FFF7FFECFF63FA53FC84F9D9.xml @@ -0,0 +1,121 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella israelensis +De Meyer, 1995 + + + + + + + + +MATERIAL EXAMINED. +Iran +: +Fars +, +Jahrom +, +28°30′31″N +53°34′21″E +, + +1044 m + +, +window trap +, + +20–25.X 2016 + +, +1♂ +, leg. +B. Majnon Jahromi. + + + + + +DISTRIBUTION. +Iran +: +Fars +(new record). – Europe (Foldvary & De Meyer, 1999). + + +NOTE. This species is recorded from +Iran +for the first time. + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF7FFECFF63FAC0FB88FA70.xml b/data/38/2D/12/382D1232FFF7FFECFF63FAC0FB88FA70.xml new file mode 100644 index 00000000000..08e1503cd19 --- /dev/null +++ b/data/38/2D/12/382D1232FFF7FFECFF63FAC0FB88FA70.xml @@ -0,0 +1,98 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella immutata +(Becker, 1913) + + + + + + + + +DISTRIBUTION. Endemic to +Iran +: Sistan and Baluchestan, between +Kūh-i-Mughak mountain +, +Kerman +(Becker, 1913), +Alborz +, Kordan ( +Kehlmaier +& +Majnon Jahromi +, 2015) + +. + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF7FFECFF63FB30FE91FAE7.xml b/data/38/2D/12/382D1232FFF7FFECFF63FB30FE91FAE7.xml new file mode 100644 index 00000000000..b16baa1f253 --- /dev/null +++ b/data/38/2D/12/382D1232FFF7FFECFF63FB30FE91FAE7.xml @@ -0,0 +1,87 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 + + + + + + + +Tomosvaryella hamata +Majnon Jahromi et Kehlmaier, 2017 + + + + + + + +DISTRIBUTION. Endemic to +Iran +: +Fars +, Jahrom, Lar, Marvdasht (Majnon Jahromi +et al +., 2017b). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF7FFECFF63FBF5FDFCFB56.xml b/data/38/2D/12/382D1232FFF7FFECFF63FBF5FDFCFB56.xml new file mode 100644 index 00000000000..9d28e4f2e0c --- /dev/null +++ b/data/38/2D/12/382D1232FFF7FFECFF63FBF5FDFCFB56.xml @@ -0,0 +1,123 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella glabrum +(Adams, 1905) + + + + + + + + +MATERIAL EXAMINED. +Iran +: +Fars +, +Jahrom +, +28°30′N +53°35′E +, + +1044 m + +, +window trap + +, + + +10–28.IX 2016 +, +1♂ +, leg. B. Majnon Jahromi. + + + + +DISTRIBUTION. +Iran +: +Alborz +, Arangeh, Kordan (Kehlmaier & Majnon Jahromi, + + +2015), +Fars +, Jahrom, Lar, Marvdasht (Majnon Jahromi +et al +., 2017). – Afrotropical region, + +North Africa, Canary Is., Near East. + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF7FFECFF63FC7AFDC2FC29.xml b/data/38/2D/12/382D1232FFF7FFECFF63FC7AFDC2FC29.xml new file mode 100644 index 00000000000..d73feb78f84 --- /dev/null +++ b/data/38/2D/12/382D1232FFF7FFECFF63FC7AFDC2FC29.xml @@ -0,0 +1,90 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella geniculata +(Meigen, 1824) + + + + + + + +DISTRIBUTION. +Iran +: +Fars +, Jahrom, Neyriz (Majnon Jahromi +et al +., 2017). – West + +Palaearctic (De Meyer 1995). + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF7FFECFF63FCEBFE1FFC98.xml b/data/38/2D/12/382D1232FFF7FFECFF63FCEBFE1FFC98.xml new file mode 100644 index 00000000000..a587682a8c1 --- /dev/null +++ b/data/38/2D/12/382D1232FFF7FFECFF63FCEBFE1FFC98.xml @@ -0,0 +1,89 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella gazliensis +Kuznetzov, 1994 + + + + + + + +DISTRIBUTION. +Iran +: +Alborz +, Kordan (Kehlmaier & Majnon Jahromi, 2015). – +Uzbekistan +(Kuznetzov, 1994). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF7FFECFF63FD64FD5FFD0F.xml b/data/38/2D/12/382D1232FFF7FFECFF63FD64FD5FFD0F.xml new file mode 100644 index 00000000000..0dc92dd72f5 --- /dev/null +++ b/data/38/2D/12/382D1232FFF7FFECFF63FD64FD5FFD0F.xml @@ -0,0 +1,102 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella freidbergi +De Meyer, 1995 + + + + + + + +DISTRIBUTION. +Iran +: +Alborz +, Arangeh, Kordan (Kehlmaier & Majnon Jahromi, 2015), + + +East Azerbaijan +, Qurigol, (Kazerani +et al +., 2017), +Fars +, Jahrom (Majnon Jahromi +et al +., + + +2017). – +Israel +(Foldvary & De Meyer, 1999). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF7FFECFF63FDD4FE10FD9B.xml b/data/38/2D/12/382D1232FFF7FFECFF63FDD4FE10FD9B.xml new file mode 100644 index 00000000000..fc67f9f8277 --- /dev/null +++ b/data/38/2D/12/382D1232FFF7FFECFF63FDD4FE10FD9B.xml @@ -0,0 +1,95 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella docta +De Meyer, 1995 + + + + + + + +DISTRIBUTION. +Iran +: +Fars +, Jahrom, Lar (Majnon Jahromi +et al +., 2017). – +Egypt +and + + +Israel +(De Meyer, 1995). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF7FFECFF63FE8DFC57FE09.xml b/data/38/2D/12/382D1232FFF7FFECFF63FE8DFC57FE09.xml new file mode 100644 index 00000000000..b99a964000a --- /dev/null +++ b/data/38/2D/12/382D1232FFF7FFECFF63FE8DFC57FE09.xml @@ -0,0 +1,133 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella demeyeri +Kuznetzov, 1993 + + + + + + + + +MATERIAL EXAMINED. +Iran +: +Fars +, +Jahrom +, +28°30′N +53°35′E +, + +1044 m + +, +window trap + +, + + +10–28.IX 2016 +, +1♂ +, leg. B. Majnon Jahromi. + + + + + +DISTRIBUTION. +Iran +: +Alborz + +, + +Kordan ( +Kehlmaier +& +Majnon Jahromi +, 2015), +Fars + +, + + +Jahrom, Lar (Majnon Jahromi +et al +., 2017). – +Egypt +(Kuznetzov, 1993). + + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF7FFECFF63FEF2FEE0FEA0.xml b/data/38/2D/12/382D1232FFF7FFECFF63FEF2FEE0FEA0.xml new file mode 100644 index 00000000000..79b8bd612d5 --- /dev/null +++ b/data/38/2D/12/382D1232FFF7FFECFF63FEF2FEE0FEA0.xml @@ -0,0 +1,92 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella dentiterebra +(Collin, 1949) + + + + + + + +DISTRIBUTION. +Iran +: +Fars +, Jahrom (Majnon Jahromi +et al +., 2017b). – +Egypt +(Collin, + +1949). + + + \ No newline at end of file diff --git a/data/38/2D/12/382D1232FFF9FFE2FF63FEF3FEACFEA5.xml b/data/38/2D/12/382D1232FFF9FFE2FF63FEF3FEACFEA5.xml new file mode 100644 index 00000000000..b7c337a06f8 --- /dev/null +++ b/data/38/2D/12/382D1232FFF9FFE2FF63FEF3FEACFEA5.xml @@ -0,0 +1,91 @@ + + + +An annotated list of the big-headed flies (Diptera: Pipunculidae) of Iran with notes on the material collected by window traps in Fars province + + + +Author + +Majnon Jahromi, B. + + + +Author + +Gheibi, M. + + + +Author + +Fallahzadeh, M. + + + +Author + +Kehlmaier, Ch. + + + +Author + +Hesami, Sh. + +text + + +Far Eastern Entomologist + + +2018 + +2018-09-10 + + +367 + + +10 +20 + + + + +http://dx.doi.org/10.25221/fee.367.2 + +journal article +10.25221/fee.367.2 +2713-2196 +7164529 +922F5EEF-C0B5-43CE-B8C2-20635CE48432 + + + + + + + +Tomosvaryella urdaensis +Kuznetzov, 1994 + + + + + + + +DISTRIBUTION. +Iran +: +Fars +, Neyriz (Majnon Jahromi +et al +., 2017). – +Kazakhstan +(Kuznetzov, 1994). + + + + \ No newline at end of file diff --git a/data/38/2D/9B/382D9B453EED5A40B744050976F31F35.xml b/data/38/2D/9B/382D9B453EED5A40B744050976F31F35.xml new file mode 100644 index 00000000000..dc6edd3883e --- /dev/null +++ b/data/38/2D/9B/382D9B453EED5A40B744050976F31F35.xml @@ -0,0 +1,98 @@ + + + +Order Rodentia - Family Sciuridae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 2 + + + +754 +818 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316535 + + + + + +Biswamoyopterus +Saha 1981 + + + + + + + +Biswamoyopterus +Saha 1981 + +, + +Bull. Zool. Surv. +India +, 4: 331 + + +. + + + + +Type Species: + +Biswamoyopterus biswasi +Saha 1981 + + + + + +Species and subspecies: +1 species: + + +Species + +Biswamoyopterus biswasi +Saha 1981 + + + + + +Discussion: +Subtribe +Pteromyina +. + + + + \ No newline at end of file diff --git a/data/38/2E/22/382E22A6DB965A4A9B03221DE1EDECB9.xml b/data/38/2E/22/382E22A6DB965A4A9B03221DE1EDECB9.xml new file mode 100644 index 00000000000..b04b8067d76 --- /dev/null +++ b/data/38/2E/22/382E22A6DB965A4A9B03221DE1EDECB9.xml @@ -0,0 +1,305 @@ + + + +Redescription of a rarely encountered species Travisa chinensis Grube, 1869 (Annelida, Travisiidae), including a description of a new species of Travisa from Amoy, China + + + +Author + +Yang, Deyuan +Institute of Marine Biology, National Taiwan Ocean University, Keelung 20224, Taiwan & College of the Environment and Ecology, Xiamen University, Xiamen 361102, Fujian, China + + + +Author + +Wu, Xuwen +Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China +wxwelegent@sina.com + + + +Author + +Wang, Zhi +College of the Environment and Ecology, Xiamen University, Xiamen 361102, Fujian, China + + + +Author + +Zhao, Xiaoyu +https://orcid.org/0000-0001-5157-7668 +College of the Environment and Ecology, Xiamen University, Xiamen 361102, Fujian, China + + + +Author + +Hwang, Jiangshiou +https://orcid.org/0000-0003-4881-1163 +Institute of Marine Biology, National Taiwan Ocean University, Keelung 20224, Taiwan +jshwang@mail.ntou.edu.tw + + + +Author + +Cai, Lizhe +College of the Environment and Ecology, Xiamen University, Xiamen 361102, Fujian, China +cailizhe@xmu.edu.cn + +text + + +ZooKeys + + +2022 + +2022-11-04 + + +1128 + + +1 +17 + + + + +http://dx.doi.org/10.3897/zookeys.1128.90020 + +journal article +http://dx.doi.org/10.3897/zookeys.1128.90020 +1313-2970-1128-1 +6FDCCA3C97AC4E83B0728BEDB9E0B2A5 +23262984D68A5D4399328C59479019BE + + + + +Travisia chinensis Grube, 1869 + + + + +Fig. 3A-C + + + + +Travisia chinensis +Grube, 1869: 66; China Sea, North-western Pacific. + + +Travisia chinensis +Augener, 1922: 38-40. + + + +Diagnosis. +Body with 30 segments and 29 chaetigers. Branchiae cirriform from chaetiger 2, more than 25 pairs. Neuropodial lappet from chaetiger 16, notopodial lappet from chaetiger 19. Annulation pattern of segments: 1-15 triannulate, 16-26 biannulate, 26-30 uniannulate. + + +Material examined. + + + +Holotype + +. + +ZMB 0629, Chinese waters ("Chinesische +Gewaesser" +), Coll. GRUBE. + + + +Description. + +Body fusiform. Whitish in alcohol. About 30 mm in length (Fig. +3A +). Prostomium twisted, anteriorly pointed (Fig. +3B +). The mouth between chaetiger 1 and chaetiger 2 (Fig. +3B +). Branchiae cirriform, except one trifid present chaetiger 10 on the right side, more than 25 pairs, start on chaetigers 2 and to at least chaetigers 26 (Fig. +3A +). Most branchiae shorter than body width. + + + +Figure 3. + +Travisia chinensis + +Grube, 1866 (holotype, ZMB 0629) +A +complete specimen in lateral view +B +anterior part in lateral view +C +posterior part in lateral view. Abbreviations: pr, prostomium; nuO, nuchal organ; mo, mouth; br, branchiae; chaet, chaetiger; IntP, interramal papilla; Pl, parapodia lateral lappet; np, nephridial pores; Py, pygidium. + + + +Chaetigers 1-15 without parapodial lappets. Chaetiger 16 with a small neuropodial lappet, below the bundle of neurochaetae on the right side of the body (Fig. +3C +). Notopodial lappet above the bundle of notochaetae starting on chaetiger 19. Notopodial and neuropodial lappets well developed from chaetiger 19, but missing on segments 29 and 30 (Fig. +3C +). Nephridial pores from chaetigers 3-14, the first four and last four small, the remainder larger (Fig. +3A +). + + +Neuropodial and notopodial chaetal rami well separated. Chaetae arising directly from body wall, with 29 chaetigers. All chaetae hair-like, smooth and without a fringe. Interramal pores from the first chaetigers segment to almost all segments except the last one segment. Segments 2-15 with three annulations, segments 16-26 with two annulations, last five segments with one annulation (Fig. +3A +). Pygidium as long as last three segments, with about 10 indentations. + + + +Remark. + +The original description of + +Travisia chinensis + +was not detailed. Thus, it was seldom compared with the other + +Travisia + +species. According to the original description, + +T. chinensis + +has one trifid branchia, while most other + +Travisia + +species have cirriform branchiae, except for + +T. arborifera + +Fauvel, 1932 from Indian Ocean and + +T. filamentosa + +Leon-Gonzalez +, 1998 from California which were reported with strongly branched branchiae. Some researchers accepted that the trifid branchia might make + +T. chinensis + +a distinctive species ( + +Kuekenthal +1887 + +; +Fauvel 1932 +), while according to our observation, the trifid branchia is also present in a specimen of +Travisia cf. pupa +from the Yellow Sea (unpublished data), which is supposed to have only cirriform branchiae. Therefore, the presence of one bifid or trifid branchia might actually be an intraspecific variation and should not be regarded as a valid characteristic in distinguishing + +Travisia + +species. + + + +Travisia chinensis + +(30 segments, 29 chaetigers) resembles the following six species in have a similar number of segments and chaetigers (29-31): + +Travisia amadoi + +Elias +et al., 2003, + +Travisia olens + +Ehlers, 1897, + +Travisia araciae + +Rizzo & Salazar-Vallejo, 2020, + +Travisia hobsonae + +Santos, 1977, + +Travisia brevis + +Moore, 1923, and + +Travisia forbesii intermedia + +Annenkova, 1937. + + + +Travisia chinensis + +differs in the start of parapodial lappets (chaetiger 19) from + +T. amadoi + +(chaetiger 12), + +T. araciae + +(chaetiger 13), and + +T. hobsonae + +(chaetiger 1). + +Travisia chinensis + +differs from + +T. brevis + +in the following morphological characters: the number of branchiae (>25 pairs in + +T. chinensis + +vs 22 pairs in + +T. brevis + +); the shape of the prostomium (conical vs short blunt cone), and segments without parapodial lappets (last four segments vs last two segments). + + + +Travisia forbesii intermedia + +and + +T. olens + +are not easily distinguished from + +T. chinensis + +more by lack of information. According to the original description, the former two lack exact data on the position of parapodial lappets, and a re-examination of the types of the two species is needed. + + + +Type locality. + +According to +Salazar-Vallejo et al. (2014) +, the type locality was probably the coastal waters of Qingdao. +Dauvin and Bellan (1994) +also stated that the holotype was from the North-western Pacific. Until now, we have not found any other specimens of + +T. chinensis + +in the seas of China, based on the materials of MBM. + + + + \ No newline at end of file diff --git a/data/38/2E/36/382E36EA2728D4FBAF231BFEEA91A22E.xml b/data/38/2E/36/382E36EA2728D4FBAF231BFEEA91A22E.xml new file mode 100644 index 00000000000..81117014b9e --- /dev/null +++ b/data/38/2E/36/382E36EA2728D4FBAF231BFEEA91A22E.xml @@ -0,0 +1,78 @@ + + + +Checklist of aquatic and marshy Monocotyledons from the Araguaia River basin, Brazilian Cerrado + + + +Author + +Oliveira, Adriana + + + +Author + +Bove, Claudia + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +7085 +7085 + + + + +http://dx.doi.org/10.3897/BDJ.4.e7085 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e7085 +1314-2828-4-7085 + + + + +Habenaria macilenta (Lindl. ex Benth.) Rchb.f. + + + +Materials + + +Type status: +Other material +. Occurrence: recordNumber: s.n.; recordedBy: +R. S. Oliveira +; Location: country: +Brazil +; countryCode: BRA; stateProvince: +Goias +; locality: + +Sao +Miguel do Araguaia- Luis Alves Tocantins road, ca. 33 Km from +Sao +Miguel do Araguaia + +; verbatimLatitude: +13°17'15.45"S +; verbatimLongitude: +50°27'54.15"W +; verbatimCoordinateSystem: degree minutes; Event: year: 1997; month: 2; day: 15; Record Level: institutionID: Universidade de +Brasilia +Herbarium; institutionCode: +(UB 19881) + + + + + \ No newline at end of file diff --git a/data/38/2E/50/382E501E628E152A69EC5BFFD22F0415.xml b/data/38/2E/50/382E501E628E152A69EC5BFFD22F0415.xml new file mode 100644 index 00000000000..928ec7824ac --- /dev/null +++ b/data/38/2E/50/382E501E628E152A69EC5BFFD22F0415.xml @@ -0,0 +1,122 @@ + + + +Annotated checklist of the recent and extinct pythons (Serpentes, Pythonidae), with notes on nomenclature, taxonomy, and distribution + + + +Author + +Schleip, Wulf D. + + + +Author + +O'Shea, Mark + +text + + +ZooKeys + + +2010 + +66 + + +29 +80 + + + + +http://dx.doi.org/10.3897/zookeys.66.683 + +journal article +http://dx.doi.org/10.3897/zookeys.66.683 +1313-2970-66-29 + + + + +Python molurus pimbura (Deraniyagala, 1945) +[subspecies inquirenda, APP7] + + + +Synonyms: + +Python molurus molurus +(Linnaeus) (part) + + +Python molurus molurus +- +Constable 1949 + + +Python molurus pimbura +- +Deraniyagala 1955 + + +Python molurus molurus +- +Stimson 1969 + + + +Distribution: + +First reported from Nunavil (Thenmarachi), Jaffna Peninsula, Sri Lanka by +Abyerami and Sivashanthini (2008) +. + + + +Remarks: + +Hoser (2004) +resurrected this taxon from the synonymy of +Python molurus molurus +without providing reasons for this action. +Deraniyagala (1945) +separated the subspecies from +Python molurus molurus +based on lower subcaudal scale counts and the irregular shape of the lateral markings. Dorsal midbody scale rows and ventral scale counts overlap those of the nominate subspecies. +Constable (1949: 124) +did not follow this placement and synonymized this taxon with the nominate subspecies, which was followed by +Stimson (1969) +. A second paper by +Deraniyagala (1955: 6) +provided a more detailed description of the subspecies. Therein, he stated that this taxon is also separated from the nominate form "in generally possessing three preoculars instead of two" or four as stated by +Wall (1921: 47) +for some Indian populations of the nominate form. There appears to be a range in preocular scale counts across India, from three in the northeast, to four in the north-center, and two in northwest ( +O'Shea +pers. obs.) but this data, from only a few specimens, requires further verification. Contrary to his findings in 1945, +Deraniyagala (1955) +reports this taxon to have "more subcaudals" than the nominate form, obviously a typographic error according to the scale count data provided therein. It seems likely that subsequent workers overlooked this latter work, since neither +Stimson (1969) +nor +McDiarmid et al. (1999) +or +Henderson and Powell (2007) +cited it. Several subsequent workers accepted the placement to the synonymy of the nominate form, but no further studies have been conducted on the molurus-complex. However, besides the lower subcaudal scale counts and the higher number of preoculars, the pink surface of the head may also constitite a morphological difference. ( +Boulenger (1890 +, +1893 +) and MA +Smith (1943) +recorded two preoculars for +Python molurus +, while +Wall (1921) +records three preoculars for specimens from Ceylon. Since Sri Lanka is a known biodiversity hot spot with a high level of endemism, this allopatric population may represent a cryptic species. Because of the evidence provided by +Deraniyagala (1955) +, these authors tentatively list this taxon as a valid subspecies and call for further research regarding its true status (APP7). + + + + \ No newline at end of file diff --git a/data/38/2E/81/382E810C9EBD3CEB49CC30CD783D93A5.xml b/data/38/2E/81/382E810C9EBD3CEB49CC30CD783D93A5.xml new file mode 100644 index 00000000000..1b71ccf9783 --- /dev/null +++ b/data/38/2E/81/382E810C9EBD3CEB49CC30CD783D93A5.xml @@ -0,0 +1,253 @@ + + + +Annotated catalog and bibliography of the cyclocephaline scarab beetles (Coleoptera, Scarabaeidae, Dynastinae, Cyclocephalini) + + + +Author + +Moore, Matthew R. +Department of Entomology and Nematology, University of Florida, Building 1881 Natural Area Drive, Steinmetz Hall, Gainesville, FL 32611, USA +cyclocephala@gmail.com + + + +Author + +Cave, Ronald D. +Department of Entomology and Nematology, University of Florida, Indian River Research and Education Center, 2199 South Rock Road, Fort Pierce, FL 34945, USA + + + +Author + +Branham, Marc A. +Department of Entomology and Nematology, University of Florida, Building 1881 Natural Area Drive, Steinmetz Hall, Gainesville, FL 32611, USA + +text + + +ZooKeys + + +2018 + +2018-03-22 + + +745 + + +101 +378 + + + + +http://dx.doi.org/10.3897/zookeys.745.23685 + +journal article +http://dx.doi.org/10.3897/zookeys.745.23685 +1313-2970-745-101 +8785DC6BC2A244FD94B6243EB07C717F +047DFFCAFFA5F32EA97C873F4708943F +1222435 + + + + +Ancognatha scarabaeoides Erichson, 1847 + + + + +Ancognatha scarabaeoides +Erichson, 1847a: 97 [original combination]. + + +Cyclocephala scarabaeoides +(Erichson) [new combination by +Lacordaire 1856 +: 398, 399]. + + +Ancognatha scarabaeoides +Erichson [revised combination by +Bates 1888 +: 297]. + + +syn. +Chalepides unduavicus +Prokofiev, 2012: 3-5 [original combination]. + + +Ancognatha scarabaeoides +Erichson [synonymy by +Prokofiev 2013 +: 131]. + + + +Types. + +Lectotype ♂ of + +A. scarabaeoides + +at ZMHB ( + +Endrodi +1966 + +). Holotype ♂ of + +C. unduavicus + +at IEE ( +Prokofiev 2012 +). + + + +Distribution. + +BOLIVIA: Cochabamba, La Paz. COLOMBIA: Antioquia, +Atlantico +, Bogota, D. C., +Boyaca +, Caldas, Cauca, Cundinamarca, Huila, Meta, +Narino +, +Quindio +, Risaralda, Santander, Tolima, Valle del Cauca. PANAMA: +Chiriqui +. PERU: Ancash, Apurimac, Cajamarca, Cusco, Huancavelica, +Huanuco +, +Junin +, La Libertad, Puno, San +Martin +. VENEZUELA. + + + +References. + +Dejean 1833 +, +1836b +, +Sturm 1843 +, +Erichson 1847a +, +1848b +, +Burmeister 1847 +, +Lacordaire 1856 +, +Marschall 1857 +, +Harold 1869b +, +Bates 1888 +, +Arrow 1937b +, +Blackwelder 1944 +, +Apolinar Maria 1946 +, +Pike et al. 1976 +, + +Endrodi +1966 + +, +1967b +, +1985a +, +Ruiz and Posada 1986 +, +Posada Ochoa 1989 +, +Ruiz and Pamalpa 1990 +, +Montoya et al. 1994 +, + +Diaz +et al. 1997 + +, +Ratcliffe 2002a +, +2003 +, Restrepo et al. 2003, + +Marino +et al. 2004 + +, +Lucero Malfa et al. 2006 +, +Neita-Moreno and Gaigl 2008 +, + +Vallejo and +Moron +2008 + +, + +Gasca-Alvarez +and +Amat-Garcia +2010 + +, +Krajcik 2005 +, +2012 +, +Breeschoten et al. 2013 +, +Prokofiev 2012 +, +2013 +, +2014 +, +Ratcliffe et al. 2015 +, + +Lopez-Garcia +et al. 2015 + +, +Figueroa and Ratcliffe 2016 +, +Villalobos-Moreno et al. 2016 +, +2017 +. + + + +Remarks. + +Prokofiev (2014) +treated +A. scarabaeoides ab. unduavica +as an infrasubspecific entity (color variant) after treating the name as a synonym ( +Prokofiev 2013 +). + + + + \ No newline at end of file diff --git a/data/38/2E/9B/382E9BD635B01CB85E5EC89C9CE2B634.xml b/data/38/2E/9B/382E9BD635B01CB85E5EC89C9CE2B634.xml new file mode 100644 index 00000000000..12d0e04d688 --- /dev/null +++ b/data/38/2E/9B/382E9BD635B01CB85E5EC89C9CE2B634.xml @@ -0,0 +1,84 @@ + + + +Order Scandentia + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +104 +109 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Dendrogale melanura +subsp. +melanura +Thomas 1892 + + + + + + + +Dendrogale melanura +subsp. +melanura +Thomas 1892 + +, +Ann. Mag. Nat. Hist., ser. 6, 9: 251 + +. + + + + +Type Locality: + +Borneo, +Sarawak +, Mt. Dulit, +5,000 ft. +( + +1,524 m + +). + + + + + \ No newline at end of file diff --git a/data/38/2E/D7/382ED72668D2590991C4A9AF7B702954.xml b/data/38/2E/D7/382ED72668D2590991C4A9AF7B702954.xml new file mode 100644 index 00000000000..415263315c4 --- /dev/null +++ b/data/38/2E/D7/382ED72668D2590991C4A9AF7B702954.xml @@ -0,0 +1,167 @@ + + + +Biting midges of Egypt (Diptera: Ceratopogonidae) + + + +Author + +El-Hawagry, Magdi S. +Entomology Department, Faculty of Science, Cairo University, Giza, Egypt +https://orcid.org/0000-0001-9162-5265 +elhawagry@gmail.com + + + +Author + +El-Azab, Salah El-Din A. +Insect Taxonomy Department, Plant Protection Research Institute, Dokki, Giza, Egypt + + + +Author + +Abdel-Dayem, Mahmoud S. +College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia +https://orcid.org/0000-0002-6276-1740 + + + +Author + +Al Dhafer, Hathal M. +College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia +https://orcid.org/0000-0002-4911-2332 + +text + + +Biodiversity Data Journal + + +2020 + +8 + + +52357 +52357 + + + + +http://dx.doi.org/10.3897/BDJ.8.e52357 + +journal article +http://dx.doi.org/10.3897/BDJ.8.e52357 +1314-2828-8-e52357 +CEB65C20D7855AD294A989CBC7F67ED6 + + + + +Bezzia Kieffer, 1899 + + + + +Bezzia + +Bezzia + +Kieffer, 1899 [ +Kieffer 1899 +: 69]. Type species: + +Ceratopogon ornatus + +Meigen, by original designation. + + +Pseudobezzia +Malloch, 1915 [ + +Malloch 1915a + +: 351]. Type species: + +Ceratopogon expolitus + +Coquillett, by original designation. + + +Allobezzia +Kieffer, 1917 [ + +Kieffer 1917 + +: 296]. Type species: + +Ceratopogon expolitus + +Coquillett, by original designation. + + +Lasiobezzia +Kieffer, 1925 [ +Kieffer 1925b +: 54]. Type species: + +Bezzia pilipennis + +Lundstroem +, by original designation. + + +Homobezzia +Macfie, 1932 [ +Macfie 1932 +: 496]. Type species: + +Homobezzia nyasae + +Macfie, by monotypy. + + +Sivabezzia +Remm, 1974 [ +Remm 1974 +: 440]. Type species: + +Bezzia campanai + +Clastrier, by original designation. + + +Pygobezzia +Remm, 1974 [ + +Remm 1974 + +: 441]. Type species: + +Bezzia strobli + +Kieffer (= + +Ceratopogon albicornis + +Meigen), by original designation. + + +Aspinabezzia +Dow and Turner, 1976 [ + +Dow and Turner 1976 + +: 122]. Type species: + +Ceratopogon glaber + +Coquillett, by original designation. + + + + \ No newline at end of file diff --git a/data/38/2F/E4/382FE4C71CFF95BB7F5E24C0DE8347C9.xml b/data/38/2F/E4/382FE4C71CFF95BB7F5E24C0DE8347C9.xml new file mode 100644 index 00000000000..76444b66212 --- /dev/null +++ b/data/38/2F/E4/382FE4C71CFF95BB7F5E24C0DE8347C9.xml @@ -0,0 +1,159 @@ + + + +A taxonomic revision of Liogenys occurring in Brazil with an interactive key and remarks on New World Diplotaxini (Coleoptera, Melolonthidae) + + + +Author + +Cherman, Mariana Alejandra + + + +Author + +Mise, Kleber Makoto + + + +Author + +Moron †, Miguel Angel + + + +Author + +Vaz-de-Mello, Fernando Z. + + + +Author + +Almeida, Lucia Massutti de + +text + + +ZooKeys + + +2017 + +699 + + +1 +120 + + + + +http://dx.doi.org/10.3897/zookeys.699.12031 + +journal article +http://dx.doi.org/10.3897/zookeys.699.12031 +1313-2970-699-1 +0F92401F3F7C4896AD9D72BC84348C7D +0F92401F3F7C4896AD9D72BC84348C7D + + + + +Liogenys laminiceps Moser, 1919 +Figs 65, 91 + + + + + +Liogenys +laminiceps + +Moser, 1919: 16 (orig. desc.); +Blackwelder 1944 +: 227 (check.); +Frey 1969 +: 38 (key); +Evans 2003 +: 210 (check.); +Evans and Smith 2005 +: 174 (check.); +Evans and Smith 2009 +: 178 (check.). + + + +Type material. + +Liogenys laminiceps +male holotype (ZMHB): [white printed] "Brasilia/ [handwritten] Sao Paulo", [white handwritten] " +Liogenys +/ +laminiceps +/Mos/Typen", [light red printed] +"Typus" +, [white printed] " +Liogenys +/ +laminiceps +/Mos.", [red printed] "HOLOTYPUS/ +Liogenys +/ +laminiceps +Moser, 1919/labelled by MNHUB 2013". Genitalia mounted. + + + +Diagnosis. +Body and elytra reddish brown; elongate, widest at posterior third; pronotum darker; clypeal emargination shallow, rounded and wide; outer sides of anterior teeth parallel; clypeal lateral margin convex, with a rounded projection, obtuse angle between outer side of anterior teeth and clypeal lateral projection; antenna 9-articulated; pronotal disc punctures very sparse; pronotal posterior corners sub-angled, obtuse; mesotibia quadrate in cross section; metafemur with thick and erect bristles on posterior margin; pygidium convex; in males, parameres widened from the midline towards the apex, maximum width subapically; apex rounded; inner margins convergent (Fig. 65F). + + +Figure 65. +Liogenys laminiceps +Moser. A Dorsal view B Lateral view C Frontal view D Clypeus and pronotum E Pygidium F Parameres, dorsal view G Parameres, lateral view. + + + + +Redescription. + +Length: 9.8 mm; width: 5.5 mm. Reddish brown. Head: distance between eyes nearly twice the width of one eye; frons shorter than clypeus; clypeus bristled anteriorly; clypeal emargination rounded, shallow and wide; outer sides of anterior teeth parallel; outer margin of anterior teeth shorter than the eye; clypeal lateral margin convex, with a rounded projection; distance between this projection and anterior tooth shorter than basal width of anterior tooth, distance between clypeal lateral projection and anterior margin of eye shorter than one eye; obtuse angle between outer side of anterior teeth and clypeal lateral projection; canthus not exceeding the outer margin of the eye; distal maxillary palpomere, maximum width slightly wider than the apex; fovea deep and elongate, extending to or past the transverse midline of the palpomere; labium transversely carinated, as wide as it is long; antenna 9-articulated, lamellae lighter in color than flagellum and equal in length. Thorax: anterior margin of pronotum straight, flanged throughout; maximum length of pronotum exceeding the length of tarsomeres I, II and III together; disc glabrous, punctures very sparse and coarse; pronotal posterior corners sub-angled, obtuse; proepisternum with long bristles; mesepisternum scaly; sides of metasternum scaly and bristled, few long bristles on the anterior margin; distance between meso- and metacoxae up +to +twice longer than the metacoxa; scutellum rounded, coarsely punctured. Elytra: shiny, glabrous, uniform reddish brown; elytra more than three times longer than the pronotum; elytral suture and elytron unicolored, distinctly elevated; all four elytral ridges barely noticeable. Legs: procoxa scaly on infra-carinal and outer surface, punctures visible at 12 +x +magnification; three protibial teeth, middle and apical equal in size, the three teeth equally spaced; protibial inner apical spur present; mesofemural disc setose, with a row of long bristles on anterior and posterior margins; mesotibia quadrate in cross section, disc finely sculptured; two mesotibial transverse carinae, the apical one incomplete; basal apophysis of metacoxa produced beyond the outer margin of trochanter; metafemur with thick and erect bristles on posterior margin; inner margin of metatibia carinated towards apex; inner surface setose; disc finely sculptured; metatibial transverse carina present posteriorly and posterior discontinuous longitudinal carina; metatibial apical spurs of different lengths, the longest equal in length to the diameter of the tibial apex; basal metatarsomere wider than tarsomere II and equal in length; protarsomere II short and wide; pro- and mesotarsomeres I to IV enlarged, protarsomeres slightly wider than the mesotarsomeres and more than twice as wide as metatarsi; claw bifid, symmetrical, superior tooth longer and as wide as the inferior; distance between teeth as long as the inferior tooth. Abdomen: band of scales visible at the lowest magnification beneath the outer margin of elytra; ventrites bristled on disc and sides; propygidium visible, bristled and scaly; pygidium convex, sub-trapezoidal, wide, pygidial width not exceeding distance between spiracles of pro +pygidium +, pygidial disc bristled throughout; pygidial apex rounded. Parameres: basal region with parameral split at 2/3; parameres widened from the midline towards the apex, maximum width subapically (Fig. 65F); apex rounded; inner margins convergent. In lateral view parameres concave (Fig. 65G). + + + +Type-locality. + +BRAZIL. +Sao +Paulo. + + + +Geographical distribution. +BRAZIL (SP). + + +Remarks. + +Liogenys laminiceps +is one of the few species with antenna 9-articulated, together with +L. sinuaticeps +(Fig. 72) and +L. flavida +, a southern Argentinian species. The last two species are easily differentiated from +L. laminiceps +because they are yellowish and with sides of body being almost parallel. The female of +L. laminiceps +remains unknown. + + + + \ No newline at end of file diff --git a/data/38/2F/EF/382FEF0BD9FA228C4F4A4759D550FB19.xml b/data/38/2F/EF/382FEF0BD9FA228C4F4A4759D550FB19.xml new file mode 100644 index 00000000000..1f99edee0a1 --- /dev/null +++ b/data/38/2F/EF/382FEF0BD9FA228C4F4A4759D550FB19.xml @@ -0,0 +1,76 @@ + + + +A new species of Microglanis Eigenmann, 1912 (Siluriformes, Pseudopimelodidae) from rio São Francisco basin, Brazil. + + + +Author + +Horácio Mori + + + +Author + +Oscar Akio Shibatta + +text + + +Zootaxa + + +2006 + +1302 + + +31 +42 + + + + +http://www.zoobank.org/urn:lsid:zoobank.org:pub:D25EBB8D-1F2D-41DB-989F-34EDC6FC0572 + +journal article +z01302p031 + + + + +Microglanis variegatus +. + + + + + +Ecuador +. +Vinces +: + +CAS +17971 + +, +Holotype +, (45.0) + +; + + +CAS +63688 + +, +Paratype +(2, 28.5-36.7) + +. + + + + \ No newline at end of file diff --git a/data/38/2F/EF/382FEF7031FB5622954B9D3F19C1B808.xml b/data/38/2F/EF/382FEF7031FB5622954B9D3F19C1B808.xml new file mode 100644 index 00000000000..baa57436d09 --- /dev/null +++ b/data/38/2F/EF/382FEF7031FB5622954B9D3F19C1B808.xml @@ -0,0 +1,68 @@ + + + +Middle Cenomanian coral fauna from the Rosssteinalmen (Northern Calcareous Alps, Bavaria, Southern Germany) - a revised and extended version + + + +Author + +Loeser, Hannes +Estacion Regional del Noroeste, Instituto de Geologia, Universidad Nacional Autonoma de Mexico, Blvd. Luis Donaldo Colosio S / N y Madrid, 83250 Hermosillo, Sonora, Mexico + + + +Author + +Werner, Winfried +SNSB - Bayerische Staatssammlung fuer Palaeontologie und Geologie and GeobioCenterLMU, Richard-Wagner-Strasse 10, D- 80333 Muenchen, Germany +werner@snsb.de + + + +Author + +Darga, Robert +Naturkunde- und Mammut-Museum Siegsdorf, Auenstrasse 2, D- 83313 Siegsdorf, Germany + +text + + +Zitteliana + + +2023 + +2023-12-20 + + +97 + + +89 +147 + + + + +http://dx.doi.org/10.3897/zitteliana.97.113796 + +journal article +http://dx.doi.org/10.3897/zitteliana.97.113796 +2747-8106-97-89 +D456441932134D3896BBE7CFE157E0F8 +0B2F9DF86A615518B1D44DBB56689406 + + + + +Family +Microsolenidae Koby, 1889 + + + +Description. +Solitary (not in the Cretaceous) and colonial (cerioid, hydnophoroid, meandroid, phaceloid, plocoid, thamnasterioid) colonies. Septa completely and regularly perforated. Interseptal space larger than or equal to septal thickness. + + + \ No newline at end of file diff --git a/data/38/30/3B/38303BFBB6BC1813AC30E693AAC562A9.xml b/data/38/30/3B/38303BFBB6BC1813AC30E693AAC562A9.xml new file mode 100644 index 00000000000..ce21a4796fd --- /dev/null +++ b/data/38/30/3B/38303BFBB6BC1813AC30E693AAC562A9.xml @@ -0,0 +1,257 @@ + + + +The genus Lycianthes (Solanaceae, Capsiceae) in Mexico and Guatemala + + + +Author + +Dean, Ellen +UC Davis Center for Plant Diversity, Plant Sciences M. S. 7, One Shields Ave., Davis, CA 95616, USA +https://orcid.org/0000-0002-5986-0027 +eadean@ucdavis.edu + + + +Author + +Poore, Jennifer +UC Davis Center for Plant Diversity, Plant Sciences M. S. 7, One Shields Ave., Davis, CA 95616, USA + + + +Author + +Anguiano-Constante, Marco Antonio +Laboratorio Nacional de Identificacion y Caracterizacion Vegetal (LaniVeg), Consejo Nacional de Ciencia y Tecnologia (CONACyT), Centro Universitario de Ciencias Biologicas y Agropecuarias, Universidad de Guadalajara, Camino Ramon Padilla Sanchez 2100, 45110 Nextipac, Zapopan, Jalisco, Mexico +https://orcid.org/0000-0003-4071-8108 + + + +Author + +Nee, Michael H. +26776 US Hwy 14, Richland Center, WI 53581, USA + + + +Author + +Kang, Hannah +UC Davis Center for Plant Diversity, Plant Sciences M. S. 7, One Shields Ave., Davis, CA 95616, USA + + + +Author + +Starbuck, Thomas +UC Davis Center for Plant Diversity, Plant Sciences M. S. 7, One Shields Ave., Davis, CA 95616, USA + + + +Author + +Rodrigues, Annamarie +UC Davis Center for Plant Diversity, Plant Sciences M. S. 7, One Shields Ave., Davis, CA 95616, USA + + + +Author + +Conner, Matthew +UC Davis Center for Plant Diversity, Plant Sciences M. S. 7, One Shields Ave., Davis, CA 95616, USA + +text + + +PhytoKeys + + +2020 + +168 + + +1 +333 + + + + +http://dx.doi.org/10.3897/phytokeys.168.51904 + +journal article +http://dx.doi.org/10.3897/phytokeys.168.51904 +1314-2003-168-1 +5F39D34A0DEF5952A2C4E9090C14B498 + + + + +7 +Lycianthes breedlovei E.Dean, Phytotaxa 409: 265. 2019 +Fig. 18 + + + +Type. + +Mexico. Chiapas: Mpio. La Independencia, third ridge along logging road from Las Margaritas to Campo Alegre, [ +16.4756 +, +-91.8234 +], 2300 m, 6 May 1973, +D. Breedlove 34793 +(holotype: CAS [480622]; isotypes: LL [00226970], MO [acc. # 2602916]). + + + +Figure 18. +Image of isotype of + +L. breedlovei + +, +Breedlove 34793 +(MO). Specimen used with permission from the Missouri Botanical Garden (http://www.tropicos.org). + + + + +Description. + +Vine to scandent shrub, 2-3.5 (5) m tall (perhaps taller, if a vine). Indument of orange to pale yellow (yellow-grey), uniseriate, multicellular, stalked, multangulate-stellate, eglandular, spreading trichomes 0.25-1.5 (2) mm long, ca. 0.75 in diameter, the rays 3-5 per whorl, straight, often rebranched, sometimes several times. Stems pale green (drying tan) when young, moderately to densely pubescent, not compressed when dried in a plant press, becoming brown and woody with age; upper sympodial branching points a mixture of monochasial and dichasial, the branching divaricate, the branches diverging at wide angles. Leaves simple, the leaves of the upper sympodia usually unpaired, if paired, then unequal in size, the larger ones with blades 3.5-10 +x +1.5-4.5 cm, the smaller ones (usually not developing) with blades 1-3.5 +x +0.5-2 cm, the leaf pairs similar in shape, the blades ovate, elliptic, or obovate, chartaceous, sparsely to densely pubescent (denser on the abaxial side, especially along the veins), the base cuneate to rounded, sometimes oblique, the margin entire, usually irregularly undulate, the apex acute to acuminate, the petiole 0.3-1 cm long, the larger leaf blades with 4-6 primary veins on each side of the midvein. Flowers solitary or in groups of 2-5, axillary, oriented horizontally; peduncles absent; pedicels 9-16 mm long and erect in flower, 10-25 mm long and erect in fruit, densely pubescent; calyx 2.5-3.5 mm long, 3.5-4.5 mm in diameter, campanulate, pale green (sometimes nearly translucent) with dark ribs, sparsely to densely pubescent, the margin truncate, with 10 spreading linear appendages 1-3 mm long emerging ca. 0.5 mm below the calyx rim; fruiting calyx enlarged, widely bowl-shaped to rotate, 2-3 mm long, 6-8 mm in diameter, the appendages to 5 mm long; corolla 0.9-1.5 cm long, rotate in orientation, shallowly stellate in outline, divided ca. 1/2 of the way to the base, with abundant interpetalar tissue, white to lilac, adaxially with darker purple stripes on the lobes, sparsely pubescent with few scattered trichomes, abaxially usually densely puberulent on the lobes (best seen in bud); stamens slightly unequal, straight, the four short filaments 0.5-1 mm long, the one long filament 1-2 mm long, glabrous, the anthers 3-4 mm long, elliptic, free of one another, yellow, sometimes pubescent on the inner face along the connective, poricidal at the tips, the pores ovate, dehiscing distally, not opening into longitudinal slits; pistil with glabrous ovary, the style 6-8 mm long, linear, straight to curved, glabrous, the stigma oblong, decurrent down two sides. Fruit a berry, 4-10 mm long, 5-11 mm in diameter, depressed globose, orange when mature, glabrous, lacking sclerotic granules. Seeds 5-30 per fruit, 3-3.5 +x +2-2.5 mm, flattened, thickened on the edges, reniform to depressed ovate in outline, usually with small notch on one side, orange, the surface reticulum with tight serpentine pattern and shallow luminae, the margin thickened and rougher in texture than the center. + + + +Chromosome number. +Unknown. + + +Distribution and habitat. + +Mexico (Chiapas), in cloud forest, often in oak forest, sometimes associated with + +Pinus + +, + +Abies + +, + +Magnolia + +, or + +Podocarpus + +, sometimes near disturbed areas, such as milpas, 2000-3000 m in elevation (Fig. +19 +). + + + +Figure 19. +Map of geographic distribution of + +L. breedlovei + +based on herbarium specimen data. + + + + +Common names and uses. + +Mexico. Chiapas: chichol mut (Tzeltal) ( + +C. +Santiz +R. 854 + +); penko antivo (Tzotzil) ( + +C. +Santiz +R. 904 + +); tunatzak (Tzeltal) ( + +A. +Medez +Ton 5054 + +). + + + +Phenology. +Flowering specimens have been collected from April through July; specimens with mature fruits have been collected from August to November. The timing of the diurnal movements of the corolla of this species is not known, but many specimens have been collected with open flowers indicating that the flowers are open for an extended period during the day. + + +Preliminary conservation status. + + +Lycianthes breedlovei + +is restricted to cloud forest habitat in the state of Chiapas, represented by 18 collections, only one of which is from a protected area. This species was previously given a preliminary assessment by +Dean et al. (2019a) +of Endangered. + + + +Discussion. + + +Lycianthes breedlovei + +is a shrub to vine with zigzag branching due to widely divaricate branching angles, yellow to orange branched pubescence, white flowers with violet markings, and unequal stamens. It is closely related to + +L. hortulana + +Standley & L.O.Williams, described from Honduras. The two species are geographically isolated from one another, with no populations of either species known to occur in Guatemala. They have diverged from one another in pedicel length ( + +L. hortulana + +flowers have pedicels 3-9 mm long vs 9-16 mm long), flower size ( + +L. hortulana + +has corollas that are 0.6-1 cm long vs 0.9-1.5 cm), corolla pubescence ( + +L. hortulana + +has very sparse pubescence on the abaxial side of the corolla lobes vs dense), and stamen length ( + +L. hortulana + +has equal stamens vs usually unequal) ( +Dean et al. 2019a +). + + + +Representative specimen examined. + +Mexico. Chiapas +: Mpio. Tenejapa, along the road to the town of Matzam, ca. 1.5 km from the eastern outskirts of the town of Las Ollas where the road forks, about 2.6 km from the intersection with the San +Cristobal +de las Casas-Tenejapa road, just west and upslope of the settlement of Paraje Cruz Tzibaltic, on ridge where there is an intersection with an undeveloped road, +16.7832 +, +-92.5275 +, 2484 m, 13 Sep 2017, +E. Dean 9531 +(DAV226596). + + + + \ No newline at end of file diff --git a/data/38/30/61/38306156309E5BA4929614E9F6B99C49.xml b/data/38/30/61/38306156309E5BA4929614E9F6B99C49.xml new file mode 100644 index 00000000000..8462d0eae78 --- /dev/null +++ b/data/38/30/61/38306156309E5BA4929614E9F6B99C49.xml @@ -0,0 +1,65 @@ + + + +Documenting museum records of West African Coccinellidae (Coleoptera) in Benin and Senegal + + + +Author + +Hounkpati, Kwevitoukoui + + + +Author + +McHugh, Joseph V. + + + +Author + +Niang, Abdoul Aziz + + + +Author + +Goergen, Georg + +text + + +Biodiversity Data Journal + + +2020 + +8 + + +47340 +47340 + + + + +http://dx.doi.org/10.3897/BDJ.8.e47340 + +journal article +http://dx.doi.org/10.3897/BDJ.8.e47340 +1314-2828-8-e47340 +239E5BBB61345409ADA8FDA43A52FDDF + + + + +Cheilomenes sulphurea (Olivier, 1791) + + + +Distribution +Angola, Cameroon + + + \ No newline at end of file diff --git a/data/38/30/87/383087B3FF80FFA1B0D2F9CA351317EE.xml b/data/38/30/87/383087B3FF80FFA1B0D2F9CA351317EE.xml new file mode 100644 index 00000000000..0960c91999c --- /dev/null +++ b/data/38/30/87/383087B3FF80FFA1B0D2F9CA351317EE.xml @@ -0,0 +1,134 @@ + + + +On Pontoniinae (Crustacea, Decapoda, Palaemonidae) collected from ascidians + + + +Author + +Fransen, Charles H. J. M. +Nationaal Natuurhistorisch Museum - Naturalis, Postbus 9517, NL- 2300 RA Leiden (The Netherlands) fransen @ naturalis. nnm. nl. + +text + + +Zoosystema + + +2006 + +28 + + +3 + + +713 +746 + + + +journal article +10.5281/zenodo.5392396 +1638-9387 +5392396 + + + + + +Periclimenaeus orbitocarinatus + +n. sp. +( +Figs 13-15 +) + + + + + +TYPE +MATERIAL + +. — + +Loyalty Islands +. + +MUSORSTOM 6, stn DW 431, +20°22.25’S +, +166°10.00’E +, +21 m +, in + +Lissoclinum verrilli +(Van Name, 1902) + +, +18.II.1989 +, coll. B. Richer de + + +Forges, 1 ovigerous + +holotype +pocl. +2.3 mm +(minor P2 missing, telson broken) (MNHN-Na 15253). + + + +Madagascar +. + +MUA 76, in + +Didemnum +sp. + +, coll. P. Laboute, 1 ovigerous + +paratype +pocl. +2.1 mm +( +RMNH +D 51002). + + + +Indonesia +. + +Manado, +15 m +, in + +Didemnum +sp. + +, +2 juvenile +paratype +specimens pocl. +1.1 mm +( +R += 2/0) and +1.4 mm +( +R += 2/0) (damaged, most pereiopods detached) (MNHN- Na 15254). + +ETYMOLOGY. — From the Latin “orbita” referring to the orbit of the eye, combined with the Latin “carina” meaning “ridge”. + +DESCRIPTION OF FEMALE +HOLOTYPE + + + + \ No newline at end of file diff --git a/data/38/30/87/383087B3FF90FFB1B0DCFEE630061195.xml b/data/38/30/87/383087B3FF90FFB1B0DCFEE630061195.xml new file mode 100644 index 00000000000..48c0832c330 --- /dev/null +++ b/data/38/30/87/383087B3FF90FFB1B0DCFEE630061195.xml @@ -0,0 +1,134 @@ + + + +On Pontoniinae (Crustacea, Decapoda, Palaemonidae) collected from ascidians + + + +Author + +Fransen, Charles H. J. M. +Nationaal Natuurhistorisch Museum - Naturalis, Postbus 9517, NL- 2300 RA Leiden (The Netherlands) fransen @ naturalis. nnm. nl. + +text + + +Zoosystema + + +2006 + +28 + + +3 + + +713 +746 + + + +journal article +10.5281/zenodo.5392396 +1638-9387 +5392396 + + + + + + +Rostronia stylirostris +( +Holthuis, 1952 +) + + + + + + + + + +Pontonia stylirostris +Holthuis, 1952: 169 + + +, figs 82-84 ( +type +locality: between Pulau Misool and New +Guinea +, +1°42.5’S +, +130°47.5’W +, +32 m +). + + + + + +Rostronia stylirostris + +– + +Fransen 2002: 260-270 + +, figs 171- 177. + + + + + +MATERIAL EXAMINED +. — + +Moçambique +. + +Ibo Island, in lagoon, in + +Ascidia sydneiensis +Stimpson, 1855 + +, +11.XI.1995 +, 1 ovigerous + +pocl. +3.1 mm +(MNHN-Na 15220). + + + +REMARKS +Rostrum with two distal dorsal teeth. Fingers of minor chelae with 10 small teeth in proximal third of cutting edge. + +The species has been recorded from the Red Sea, +Oman +and, Tanganyika, +Australia +, Misool, +Indonesia +, and New +Guinea +. This is the first record of the species for +Moçambique +. + + +Except for the reference to a “black ascidian” for the specimen from the Red Sea ( +Fransen 2002: 270 +) no hosts are known. + +Ascidia sydneiensis + +constitutes a new host record. + + + + \ No newline at end of file diff --git a/data/38/30/87/383087B3FF90FFB1B0DFFBAE30B8140F.xml b/data/38/30/87/383087B3FF90FFB1B0DFFBAE30B8140F.xml new file mode 100644 index 00000000000..26efdf1482d --- /dev/null +++ b/data/38/30/87/383087B3FF90FFB1B0DFFBAE30B8140F.xml @@ -0,0 +1,110 @@ + + + +On Pontoniinae (Crustacea, Decapoda, Palaemonidae) collected from ascidians + + + +Author + +Fransen, Charles H. J. M. +Nationaal Natuurhistorisch Museum - Naturalis, Postbus 9517, NL- 2300 RA Leiden (The Netherlands) fransen @ naturalis. nnm. nl. + +text + + +Zoosystema + + +2006 + +28 + + +3 + + +713 +746 + + + +journal article +10.5281/zenodo.5392396 +1638-9387 +5392396 + + + + + + +Dactylonia anachoreta +( +Kemp, 1922 +) + + + + + + + + + +Pontonia anachoreta +Kemp, 1922: 264 + + +, figs 93-95 ( +type +locality: off Madras coast, +37 m +, in ascidian). + + + + + +Dactylonia anachoreta + +– + +Fransen 2002: 271-282 + +, figs 178-184. + + + + + +MATERIAL EXAMINED +. — + +Yemen +. + +Socotra, in + +Polycarpa arnoldi +(Michaelsen, 1914), 1995 + +, coll. Monniot, 1 ovigerous + +pocl. +3.4 mm +(MNHN-Na 15221). + + + +REMARKS +The specimen misses the major second chela. It can be easily identified by the long setae on the gaping fingers of the minor second pereiopod. + + +Dactylonia anachoreta + +is known from various localities in the Indian Ocean. + + + + \ No newline at end of file diff --git a/data/38/30/87/383087B3FF90FFB1B2F2FF2535C717E9.xml b/data/38/30/87/383087B3FF90FFB1B2F2FF2535C717E9.xml new file mode 100644 index 00000000000..10e6a40a7d3 --- /dev/null +++ b/data/38/30/87/383087B3FF90FFB1B2F2FF2535C717E9.xml @@ -0,0 +1,239 @@ + + + +On Pontoniinae (Crustacea, Decapoda, Palaemonidae) collected from ascidians + + + +Author + +Fransen, Charles H. J. M. +Nationaal Natuurhistorisch Museum - Naturalis, Postbus 9517, NL- 2300 RA Leiden (The Netherlands) fransen @ naturalis. nnm. nl. + +text + + +Zoosystema + + +2006 + +28 + + +3 + + +713 +746 + + + +journal article +10.5281/zenodo.5392396 +1638-9387 +5392396 + + + + + + +Dactylonia ascidicola +( +Borradaile, 1898 +) + + + + + + + + + +Pontonia ascidicola +Borradaile, 1898: 389 + + +( +type +locality: Blanche Bay, +New Britain +, in ascidian). + + + + + +Dactylonia ascidicola + +– + +Fransen 2002: 282-295 + +, figs 185-193, pls 11, 12. + + + + + + +MATERIAL EXAMINED +. — + +Papua New Guinea +. + +9°44.01’S +, +150°44.41’E +, in + +Phallusia julinea +Sluiter, 1919 + +, 30 m, + +13.I.2002 + +, coll. +CRRF +, 1 ovigerous + +pocl. +3.1 mm + +; +1 ♂ +pocl. +2.6 mm +(MNHN-Na 15222). + + +Cyclone Reef, +9°07.94’S +, +149°29.32’E +, crevice at +120 m +, “trouvée à moitié sortie de l’oscule d’une ascidie du genre + +Rhopalaea + +”, diving, +1 juvenile +pocl. +2.2 mm +(MNHN-Na 15224). + + + +Philippines +. + +Bohol +Sea, +Camiguin +Island, W side of White Island, off-shore sand cay, +9°15.38’N +, +124°39.12’E +, +18 m +, in + +Ascidia ornata +Monniot & Monniot, 2001 + +(see +Monniot & Monniot 2001: 306 +), +19.IV.1997 +, coll. +CRRF +, 1 ovigerous + +pocl. +4.3 mm +; +1 ♂ +pocl. +3.8 mm +(MNHN-Na 15223). + + +Tahiti. + +Ascidia divisa +Tokioka, 1953 + +, date unknown, +1 ♂ +pocl. +1.7 mm +; 1 ovigerous + +pocl. 2.0 mm; +1 ♂ +pocl. +1.7 mm +; +1 juvenile +pocl. +1.4 mm +(MNHN-Na 8226). + +REMARKS + +The small specimen (MNHN-Na 15224) from +Papua New Guinea +has an aberrant telson with the left distal dorsal spine position occupied by two instead of one spine. + + +The species has been recorded from + +Ascidia empheres +Sluiter, 1895 + +, + +Ascidia sydneiensis + +and + +Rhopalaea crassa +(Herdman, 1880) + +. + +Phallusia julinea + +, + +Ascidia divisa + +, and + +Ascidia ornata + +constitute new host records. + + +The species has been recorded from the Indo- West Pacific from the Red Sea and +Madagascar +to +Indonesia +, the +Philippines +, New +Guinea +, and as far east as +Guam +and the +Bismarck Archipelago +. This is the first record of the species from Tahiti. + + + + \ No newline at end of file diff --git a/data/38/30/87/383087B3FF90FFB6B31EFA0A30C41655.xml b/data/38/30/87/383087B3FF90FFB6B31EFA0A30C41655.xml new file mode 100644 index 00000000000..61bfea404f3 --- /dev/null +++ b/data/38/30/87/383087B3FF90FFB6B31EFA0A30C41655.xml @@ -0,0 +1,254 @@ + + + +On Pontoniinae (Crustacea, Decapoda, Palaemonidae) collected from ascidians + + + +Author + +Fransen, Charles H. J. M. +Nationaal Natuurhistorisch Museum - Naturalis, Postbus 9517, NL- 2300 RA Leiden (The Netherlands) fransen @ naturalis. nnm. nl. + +text + + +Zoosystema + + +2006 + +28 + + +3 + + +713 +746 + + + +journal article +10.5281/zenodo.5392396 +1638-9387 +5392396 + + + + + + +Dactylonia holthuisi +Fransen, 2002 + + + + + + + + + +Dactylonia holthuisi +Fransen, 2002: 295-306 + + +, figs 194- 201, pl. 13A ( +type +locality: +Ambon +, +Indonesia +, +03°45’S +, +128°09’E +, +25 m +). + + + + + +MATERIAL EXAMINED +. — + +Papua New Guinea +. + +Normanby Island, +10°06.33’S +, +150°57.68’E +, +18 m +, in ascidian + +Plurella colini +Monniot & Monniot, 2004 + +(see +Monniot + + +& + +Monniot 2004: 1), + +19.I.2002 + +, coll. +CRRF +, +3 ♂♂ +pocl. 1.3, 2.0, +2.1 mm + +; 3 ovigerous +♀♀ +pocl. 1.6, 1.6, +1.8 mm +(MNHN-Na 15225). + + + +02°39.49’S +, +150°25.56’E +, + +15 m + +, in ascidian + +Plurella monogyna +Monniot & Monniot, 2000 + +, + +2.VII.2003 + +, coll. +CRRF +, 1 non-ovigerous + +pocl. +1.7 mm + +; 1 ovigerous + +pocl. +1.8 mm +(MNHN-Na 15228). + + + +02°39.49’S +, +150°25.56’E +, + +15 m + +, in ascidian + +Plurella + +, + +2.VII.2003 + +, coll. +CRRF +, +2 ♂♂ +pocl. 1.1 and +1.5 mm + +; 1 ovigerous + +pocl. +1.6 mm +(MNHN-Na 15226). + + + +Ndrova Island +, +02°12.86’S +, +147°13,68’E +, + +30 m + +, in ascidian + +Plurella monogyna + +, + +24.VI.2003 + +, coll. +CRRF +, +1 ♂ +pocl. +1.8 mm + +; 1 ovigerous + +pocl. +1.8 mm +(MNHN-Na 15227). + + + +REMARKS + +This species is similar to + +Dactylonia monnioti +( +Bruce, 1990 +) + +from which it differs in not having a subdistal ventral tooth on the rostrum. None of the present specimens has a small ventral subdistal tooth on the rostrum as in the +holotype +specimen of + +D. monnioti +( +Bruce, 1990 +) + +. + + +The species has only been recorded from +Bali +and +Ambon +, +Indonesia +. These are the first records of the species from +Papua New Guinea +. + + +The species has been recorded from the genus + +Plurella + +, but without the identification of the host to species level. This is the first record of the species from + +Plurella monogyna + +. + + + + \ No newline at end of file diff --git a/data/38/30/87/383087B3FF91FFB0B303FCC335DB144E.xml b/data/38/30/87/383087B3FF91FFB0B303FCC335DB144E.xml new file mode 100644 index 00000000000..b97f04e3df8 --- /dev/null +++ b/data/38/30/87/383087B3FF91FFB0B303FCC335DB144E.xml @@ -0,0 +1,146 @@ + + + +On Pontoniinae (Crustacea, Decapoda, Palaemonidae) collected from ascidians + + + +Author + +Fransen, Charles H. J. M. +Nationaal Natuurhistorisch Museum - Naturalis, Postbus 9517, NL- 2300 RA Leiden (The Netherlands) fransen @ naturalis. nnm. nl. + +text + + +Zoosystema + + +2006 + +28 + + +3 + + +713 +746 + + + +journal article +10.5281/zenodo.5392396 +1638-9387 +5392396 + + + + + + +Ascidonia quasipusilla +( +Chace, 1972 +) + + + + + + + + + +Pontonia quasipusilla +Chace, 1972: 41-43 + + +, fig. 10. + + + + + +Ascidonia quasipusilla + +– + +Fransen 2002: 248-258 + +, figs 163-170, pls 9, 10. + + + + + +MATERIAL EXAMINED +. — + +Guadeloupe +. + +Caribbean Sea, Marina, Rivière Sens, in + +Pyura momus +(Savigny, 1816) + +(probably erroneous identification, see Remarks), date unknown, +1 ♂ +pocl. +2.2 mm +(MNHN-Na 8231). — Rivière Sens, in + +Microcosmus exasperatus +Heller, 1878 + +, date unknown, 1 ovigerous + +pocl. +4.1 mm +(MNHN-Na 8227). + + + +REMARKS + +The species has been recorded from +Martinique +and +Antigua Island +in the Caribbean and from the Mauritanian coast in the East Atlantic. This is the first record of the species for +Guadeloupe +. + + +The host + +Pyura momus + +is a synonym of + +Herdmania momus +Savigny, 1816 + +. This species is restricted to the Indo-West Pacific. According to P. Kott (pers. comm. A. J. Bruce) the ascidian species from +Guadeloupe +, which is figured by +Monniot (1983) +, is different from + +H. momus + +s.s. +The species is clearly a species of + +Herdmania + +and not of + +Pyura + +. + + + + \ No newline at end of file diff --git a/data/38/30/87/383087B3FF92FFB0B308F9CA3017142F.xml b/data/38/30/87/383087B3FF92FFB0B308F9CA3017142F.xml new file mode 100644 index 00000000000..b02c0e341bc --- /dev/null +++ b/data/38/30/87/383087B3FF92FFB0B308F9CA3017142F.xml @@ -0,0 +1,226 @@ + + + +On Pontoniinae (Crustacea, Decapoda, Palaemonidae) collected from ascidians + + + +Author + +Fransen, Charles H. J. M. +Nationaal Natuurhistorisch Museum - Naturalis, Postbus 9517, NL- 2300 RA Leiden (The Netherlands) fransen @ naturalis. nnm. nl. + +text + + +Zoosystema + + +2006 + +28 + + +3 + + +713 +746 + + + +journal article +10.5281/zenodo.5392396 +1638-9387 +5392396 + + + + + + +Ascidonia flavomaculata +( +Heller, 1864 +) + + + + + + + + + +Pontonia flavomaculata +Heller, 1864: 51 + + +( +type +locality: Adriatic Sea). + + + + + +Ascidonia flavomaculata + +– + +Fransen 2002: 215-227 + +, figs + + +137-147, pls 7, 8. + + + + +MATERIAL EXAMINED +. — + +Lebanon +. + +Rmaïlé +, + +40 m + +, in + +Ascidia mentula +Müller, 1776 + +, + +2.IX.1993 + +, collected by +Bitar +, +1 ♂ +pocl. +2.8 mm + +; 1 non-ovigerous + +pocl. +3.8 mm +(MNHN-Na 15216). + + + +REMARKS + +The species has been recorded from NE Atlantic from +Morocco +to the Gulf of +Guinea +and from the western Mediterranean as far east as the Aegean Sea. This is the first record of the species from the eastern Mediterranean. + + + +FIG. 1. — + +Ascidonia miserabilis +( +Holthuis,1951 +) + +, ♂, pocl. 1.7 mm, Guadeloupe (MNHN-Na 8228),chela of minor second pereiopod. Scale bar: 0.6 mm. + + + +The species is known to associate with various species in the +Cionidae +and +Ascidiidae +. + + + + + +Ascidonia miserabilis +( +Holthuis, 1951 +) + +( +Fig. 1 +) + + + + + +Pontonia miserabilis +Holthuis, 1951: 148 + + +, pl. 47, figs d-i ( +type +locality: off +Vieques +, +Puerto Rico +). + + + + + +Ascidonia miserabilis + +– + +Fransen 2002: 227-236 + +, figs 148-154. + + + + + + +MATERIAL EXAMINED +. — + +Guadeloupe +. + +Anse de Baille +, +Argent +face sud, date unknown, in + +Ascidia interrupta +Heller, 1878 + +, +1 ♂ +pocl. +1.7 mm + +; 1 ovigerous + +pocl. +1.7 mm +(MNHN-Na 8228). + + + +REMARKS + +Both specimens with all pereiopods detached. The largest minor chela, probably belonging to the male specimen as the chelae are relatively larger in males than in females compared to the postorbital carapace length, is different from those described by +Fransen (2002) +in which the fingers of the minor chela possess “several indistinct small teeth in proximal part of concave cutting edges”. The dactylus as well as the fixed finger of the largest minor chela have one distinct proximal tooth ( +Fig. 1 +). The smaller minor chela, probably of the female, has the dactylus with one distinct proximal tooth and the fixed finger with one distinct proximal tooth followed by few indistinct teeth proximally. + + + + \ No newline at end of file diff --git a/data/38/30/87/383087B3FF96FFB7B10CFF25300B1709.xml b/data/38/30/87/383087B3FF96FFB7B10CFF25300B1709.xml new file mode 100644 index 00000000000..060fb0ef542 --- /dev/null +++ b/data/38/30/87/383087B3FF96FFB7B10CFF25300B1709.xml @@ -0,0 +1,152 @@ + + + +On Pontoniinae (Crustacea, Decapoda, Palaemonidae) collected from ascidians + + + +Author + +Fransen, Charles H. J. M. +Nationaal Natuurhistorisch Museum - Naturalis, Postbus 9517, NL- 2300 RA Leiden (The Netherlands) fransen @ naturalis. nnm. nl. + +text + + +Zoosystema + + +2006 + +28 + + +3 + + +713 +746 + + + +journal article +10.5281/zenodo.5392396 +1638-9387 +5392396 + + + + + + +Odontonia maldivensis + +n. sp. + + + + + +( +Figs 2-5 +) + + + + + +TYPE MATERIAL +. — + +Maldives +. + +S +Malé +Atoll +, ocean side +North +reef, +04°07.54’N +, +73°30.55’E +, + +10 m + +, in + +Polycarpa cryptocarpa +(Sluiter, 1885) + +( +MHNH +S1 +POL +. +B 390 +, see +Monniot & Monniot 2001: 324 +), + +24.IX.1997 + +, coll. +CRRF +, 1 ovigerous + +holotype +pocl. +2.5 mm + +; +1 ♂ +allotype +pocl. +2.2 mm +(MNHN-Na 15236). + + +In + +Polycarpa +sp. + +, +III.2001 +, coll. C. Monniot, +1 ♂ +paratype +pocl. +1.6 mm +; + +1 ovigerous + +paratype +pocl. +2.9 mm +( +RMNH +D 51001) + +. + + + +ETYMOLOGY. — The species is named “maldivensis”, after the locality where it was first recorded. + + + +DISTRIBUTION. — Indo-West Pacific: +Maldives +. + + + +DESCRIPTION +Body subcylindrical, somewhat depressed. Carapace smooth. Rostrum well developed, without dorsal teeth, overreaching antennular peduncle, reaching level of distal margin of scaphocerite, with broad, indistinct, shallow dorsal elevation over entire length and acute lateral carinae, with slightly straight to lightly convex ventral carina in distal part; distal end acute in lateral view, without subdistal ventral tooth, with few distal setae, blunt in dorsal view, broadened at base. Inferior orbital angle produced, directed inward. Antennal spine blunt, protruding rounded process, not separated by notch from inferior orbital angle. Anterolateral margin slightly produced, anterolateral angle not produced. +Abdomen smooth; sixth segment about 1.1 times longer than fifth, 1.6 times broader than long, posteroventral angle acute, posterolateral angle feebly produced, blunt; pleura of first five segments broadly rounded. + + + \ No newline at end of file diff --git a/data/38/30/87/383087B3FF98FFB9B329FBCD320514EF.xml b/data/38/30/87/383087B3FF98FFB9B329FBCD320514EF.xml new file mode 100644 index 00000000000..317db34415d --- /dev/null +++ b/data/38/30/87/383087B3FF98FFB9B329FBCD320514EF.xml @@ -0,0 +1,131 @@ + + + +On Pontoniinae (Crustacea, Decapoda, Palaemonidae) collected from ascidians + + + +Author + +Fransen, Charles H. J. M. +Nationaal Natuurhistorisch Museum - Naturalis, Postbus 9517, NL- 2300 RA Leiden (The Netherlands) fransen @ naturalis. nnm. nl. + +text + + +Zoosystema + + +2006 + +28 + + +3 + + +713 +746 + + + +journal article +10.5281/zenodo.5392396 +1638-9387 +5392396 + + + + + + +Odontonia sibogae +( +Bruce, 1972 +) + + + + + + + + + +Pontonia sibogae +Bruce, 1972: 182 + + +, fig. 1 ( +type +locality: Curtis Channel, Port Curtis, +Queensland +, +Australia +). + + + + + +Odontonia sibogae + +– + +Fransen 2002: 371-382 + +, figs 241- 246, pl. 19. + + + + + +MATERIAL EXAMINED +. — + +Papua New Guinea +. + +Brooker Channel, +11°03.09’S +, +152°28.62’E +, +3 m +, in + +Polycarpa aurata +(Quoy & Gaimard, 1834) + +, + +1. +VI +.1998 + +, coll. +CRRF +, +1 ♂ +pocl. +4.3 mm +(MNHN-Na 15240). + + + +REMARKS +All except one ambulatory pereiopods missing, remaining pereiopod detached, with dactylus broken. + +The species has been recorded from various places in the Indo-West Pacific, from along the East African coast to +Indonesia +, +Australia +and +New Caledonia +. This is the first record of the species from +Papua New Guinea +. + + + + \ No newline at end of file diff --git a/data/38/30/87/383087B3FF9FFFBFB30EF9EB30131157.xml b/data/38/30/87/383087B3FF9FFFBFB30EF9EB30131157.xml new file mode 100644 index 00000000000..e4793f7545e --- /dev/null +++ b/data/38/30/87/383087B3FF9FFFBFB30EF9EB30131157.xml @@ -0,0 +1,176 @@ + + + +On Pontoniinae (Crustacea, Decapoda, Palaemonidae) collected from ascidians + + + +Author + +Fransen, Charles H. J. M. +Nationaal Natuurhistorisch Museum - Naturalis, Postbus 9517, NL- 2300 RA Leiden (The Netherlands) fransen @ naturalis. nnm. nl. + +text + + +Zoosystema + + +2006 + +28 + + +3 + + +713 +746 + + + +journal article +10.5281/zenodo.5392396 +1638-9387 +5392396 + + + + + + +Pseudopontonia minuta +( +Baker, 1907 +) + + + + + + + + + +Pontonia minuta +Baker, 1907: 189 + + +, pl. 24, figs 9-12 ( +type +locality: +South Australia +). — +Borradaile 1917: + + + +392. — +Hale 1927: 57 +, fig. 51. — +Holthuis 1952 +: + + + +Fransen C. H. J. M. + +15. — +Bruce 1972: 65-75 +, figs 1-5; 1976a: 92; 1983a: 211. — +Chace & Bruce 1993: 62 +. + + + + + + +Pseudopontonia minuta + +– + +Bruce 1992: 1273 + +; + +1994: 133 + +, fig. 62. — + +Li 2000: 280-281 + +. — + +Davie 2002: 337-338 + +. — + +Bruce 2002b: 112-114 + +, fig. 2. + + + + + + +MATERIAL EXAMINED +. — + +Moçambique +. + +Ibo Island +, falaise +de Matemo +, + +20 m + +, in + +Polycarpa nigricans +(Heller, 1878) + +, + +18.XI.1995 + +, 1 non-ovigerous + +pocl. +4.4 mm + +; +1 ♂ +pocl. +3.4 mm +(MNHN-Na 15242). + + + +REMARKS + +The species was hitherto only known from +South Australia +, +New South Wales +and +Queensland +. This is the first record of the species from the Indian Ocean. The identity of the host was established by +Bruce (2002b) +, being the Ascidian + +Polycarpa flava +Kott, 1985 + +. + +Polycarpa nigricans + +constitutes a new host record. + + + + \ No newline at end of file diff --git a/data/38/30/D2/3830D2C8791EB0CA53004E9F46908928.xml b/data/38/30/D2/3830D2C8791EB0CA53004E9F46908928.xml new file mode 100644 index 00000000000..c5c3654b92a --- /dev/null +++ b/data/38/30/D2/3830D2C8791EB0CA53004E9F46908928.xml @@ -0,0 +1,136 @@ + + + +Family-group names in Coleoptera (Insecta) + + + +Author + +Bouchard, Patrice + + + +Author + +Bousquet, Yves + + + +Author + +Davies, Anthony E. + + + +Author + +Alonso-Zarazaga, Miguel A. + + + +Author + +Lawrence, John F. + + + +Author + +Lyal, Chris H. C. + + + +Author + +Newton, Alfred F. + + + +Author + +Reid, Chris A. M. + + + +Author + +Schmitt, Michael + + + +Author + +Ślipinski, S. Adam + + + +Author + +Smith, Andrew B. T. + +text + + +ZooKeys + + +2011 + +88 + + +1 +972 + + + + +http://dx.doi.org/10.3897/zookeys.88.807 + +journal article +http://dx.doi.org/10.3897/zookeys.88.807 +1313-2970-88-1 + + + + +Tribe +Mesoptiliini Lacordaire, 1863 + + + + + +Mesoptilides + +Lacordaire, 1863: 563 [stem: Mesoptili-]. Type genus: +Mesoptilius +Labram and Imhoff, 1845. Comment: original vernacular name available (Art. 11.7.2): first used in latinized form by Pascoe (1870b: 436, as +Mesoptilinae +[incorrect stem formation]), generally accepted as in Alonso-Zarazaga and Lyal (1999: 193, as +Mesoptiliini +); incorrect original stem formation, not in prevailing usage. + + +Cnemidophorini +Hustache, 1937: 199, in key [stem: Cnemidophor-]. Type genus: +Cnemidophorus +Schoenherr +, 1835 [preoccupied genus name, not +Cnemidophorus +Wagler, 1830 [Reptilia]; syn. of +Cnemidontus +Schenkling, 1935]. Comment: permanently invalid (Art. 39): based on preoccupied type genus. + + +Cnemidontini +Kuschel, 1955: 271 [stem: Cnemidont-]. Type genus: +Cnemidontus +Schenkling, 1935. Comment: replacement name for +Cnemidophorini +Hustache, 1937 because of the homonymy of the type genus. + + + + \ No newline at end of file diff --git a/data/38/30/F2/3830F25DD604C80E2483FCD4C583FBF4.xml b/data/38/30/F2/3830F25DD604C80E2483FCD4C583FBF4.xml new file mode 100644 index 00000000000..796c64e71ff --- /dev/null +++ b/data/38/30/F2/3830F25DD604C80E2483FCD4C583FBF4.xml @@ -0,0 +1,141 @@ + + + +Taxonomic studies in the genus Haplanthodes (Acanthaceae) + + + +Author + +Deshmukh, Pradip Vikram + + + +Author + +Surveswaran, Siddharthan +0000-0002-6824-981X +Department of Life Sciences, CHRIST (Deemed to be University), Bengaluru, India. & siddharthan. s @ christuniversity. in; https: // orcid. org / 0000 - 0002 - 6824 - 981 X +siddharthan.s@christuniversity.in + + + +Author + +Gore, Ramchandra Dnyanoba +0000-0001-7662-6446 +Walchand College of Arts and Science, Solapur, Maharashtra, India. & ramdgore @ gmail. com; https: // orcid. org / 0000 - 0001 - 7662 - 6446 +ramdgore@gmail.com + + + +Author + +Lekhak, Manoj Madhwanand +0000-0001-5753-2225 +Angiosperm Taxonomy Laboratory, Dept. of Botany, Shivaji University, Kolhapur, Maharashtra, India. & mml _ botany @ unishivaji. ac. in; https: // orcid. org / 0000 - 0001 - 5753 - 2225 +mml_botany@unishivaji.ac.in + +text + + +Phytotaxa + + +2021 + +2021-08-26 + + +516 + + +3 + + +201 +222 + + + + +http://dx.doi.org/10.11646/phytotaxa.516.3.1 + +journal article +10.11646/phytotaxa.516.3.1 +1179-3163 +5372865 + + + + + + +Key to species of + +Haplanthodes + + + + + + + + + +1. Cladodes stout, spiny..................................................................................................................................................... + +H +. +verticillata + + + + +- Cladodes slender, not spiny ................................................................................................................................................................2 + + + + + +2. Feathery hairs present only on the lower half of the cladode; calyx 1/2 the length of corolla; cladodes up to +1.8 cm +long ............... ........................................................................................................................................................................................... + +H +. +plumosa + + + + + +- Feathery hairs absent on the cladode; calyx 1/4 the length of corolla; cladodes up to +3 cm +long .....................................................3 + + + + + + +3. Ovary glabrous; bracts equal to length of calyx; cladodes 2–4 times longer than the length of corolla; seeds with micro-papillae .. ....................................................................................................................................................................................... + +H +. +tentaculata + + + + + +- Ovary hairy; bracts shorter than the length of calyx; cladodes equal or shorter than the length of corolla; seeds without micropapillae .................................................................................................................................................................. + +H. neilgherryensis + + + + + + + \ No newline at end of file diff --git a/data/38/30/F8/3830F8B2D4325631B60275E0E57D3A42.xml b/data/38/30/F8/3830F8B2D4325631B60275E0E57D3A42.xml new file mode 100644 index 00000000000..831d54930d5 --- /dev/null +++ b/data/38/30/F8/3830F8B2D4325631B60275E0E57D3A42.xml @@ -0,0 +1,124 @@ + + + +Review of recent taxonomic changes to the emerald moths (Lepidoptera: Geometridae: Geometrinae) + + + +Author + +Plotkin, David +Department of Entomology and Nematology, University of Florida, Gainesville, United States of America & Florida Museum of Natural History, Gainesville, United States of America +https://orcid.org/0000-0002-2339-655X +dplotkin@ufl.edu + + + +Author + +Kawahara, Akito Y. +Florida Museum of Natural History, Gainesville, United States of America +https://orcid.org/0000-0002-3724-4610 + +text + + +Biodiversity Data Journal + + +2020 + +8 + + +52190 +52190 + + + + +http://dx.doi.org/10.3897/BDJ.8.e52190 + +journal article +http://dx.doi.org/10.3897/BDJ.8.e52190 +1314-2828-8-e52190 +4EE598BC99D8506FB10BD389A32B5A60 + + + + +Aoshakuna Matsumura, 1925 ("stat. rev.") + + + + +Nipponogelasma +Inoue, 1946 ("syn. nov.") + + +Aoshakuna lucia +(Thierry-Mieg, 1916) ("comb. nov.") + + +Aoshakuna sachalinensis +Matsumura, 1925 ("syn. nov.") + + +Aoshakuna lucia ussurica +Beljaev, 2007 ("ssp. nov.") + + + +Notes + +One new subspecies was described ( +Beljaev 2007 +). + + + +Aoshakuna + +was previously a junior synonym of + +Chlorissa + +Stephens, but was re-instated by +Beljaev (2007) +. In the same revision, +Beljaev (2007) +subsequently designated + +Nipponogelasma + +a junior synonym of + +Aoshakuna. + +As a result of this synonymy, + +Nipponogelasma lucia + +was transferred to + +Aoshakuna + +, creating the new combination + +A. lucia + +. +Beljaev (2007) +then synonymised this species with + +A. sachalinensis + +, the type species of + +Aoshakuna + +. + + + + \ No newline at end of file diff --git a/data/38/31/08/383108942FF743B6EBAEFDF9A2329569.xml b/data/38/31/08/383108942FF743B6EBAEFDF9A2329569.xml new file mode 100644 index 00000000000..796b8c6d8de --- /dev/null +++ b/data/38/31/08/383108942FF743B6EBAEFDF9A2329569.xml @@ -0,0 +1,634 @@ + + + +Order Rodentia - Family Muridae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 2 + + + +1189 +1531 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316535 + + + + + +Aethomys +Thomas 1915 + + + + + + + +Aethomys +Thomas 1915 + +, +Ann. Mag. Nat. Hist., ser. 8, 16: 477 + +. + + + + +Type Species: + +Epimys hindei +Thomas 1902 + + + + + +Species and subspecies: +9 species: + + +Species + +Aethomys bocagei +(Thomas 1904) + + + +Species + +Aethomys chrysophilus +(de Winton 1896) + + + +Species + +Aethomys hindei +(Thomas 1902) + + + +Species + +Aethomys ineptus +( +Thomas and Wroughton 1908 +) + + + +Species + +Aethomys kaiseri +( +Noack 1887 +) + + + +Species + +Aethomys nyikae +(Thomas 1897) + + + +Species + +Aethomys silindensis +Roberts 1938 + + + +Species + +Aethomys stannarius +(Thomas 1913) + + + +Species + +Aethomys thomasi +(de Winton 1897) + + + + + +Discussion: + + +Aethomys + +Division. An isolated member of an apparently monophyletic Subsaharan murine radiation as estimated by albumin immunology ( + +Watts and Baverstock, 1995 +a + +), but included in an + +Arvicanthis + +Division by +Misonne (1969) +, who focused on molar occlusal patterns. Analyses of mtDNA sequences (cytochrome +b +and 12S and 16S gene fragments) placed + +Aethomys + +as the basal member of an African murine clade containing + +Grammomys + +, + +Hybomys + +, + +Dasymys +, +Leminiscomys + +, + +Rhabdomys + +, + +Desmomys + +, + +Pelomys + +, + +Mylomys + +, and + +Arvicanthis +( +Ducroz et al., 2001 +) + +. The affinity with + +Arvicanthis + +, + +Hybomys + +, and + +Grammomys + +is supported by DNA/DNA hybridization (Chevret, 1994). + +Aethomys + +was originally proposed as subgenus of + +Epimys + +(= + +Rattus + +), then elevated to generic rank (see G. M. +Allen, 1939:267 +). The genus was first reviewed by +Ellerman (1941) +, then + +Davis (1975 +b +) + +, and most recently Chimimba (1998) and +Chimimba et al. (1999 +; also see below), but some species-complexes still require careful systematic revision, particularly taxa extralimital to the Southern African Subregion, to understand species-diversity and their geographic distributions, intraspecific variation, and interspecific phylogenetic relationships. The large-bodied, short-tailed members of the + +A. kaiseri + +complex ( + +A. hindei + +, + +A. kaiseri + +, + +A. thomasi + +, and + +A. stannarius + +), for example, may comprise a monophyletic unit, is considered such by +Crawford-Cabral (1998 +, 1999; as a superspecies) based upon morphology, but integrity of the grouping requires testing by analyses of molecular and other kinds of data. + + + +Micaelamys + +, diagnosed as a subgenus of + +Rattus + +by +Ellerman (1941) +primarily by dental traits, has been traditionally and is currently used as a subgenus for + +A. granti + +and + +A. namaquensis + +, with few exceptions ( +Senut et al., 1992 +). The two species are set apart from all other + +Aethomys + +by length of tail relative to body length and pelage coloration ( + +Davis, 1975 +b + +), cranial morphology (Chimimba, 1997; +Chimimba et al., 1999 +), dental traits ( +Ellerman, 1941 +; +Misonne, 1969 +), chromosomal characteristics ( +Matthey, 1954 +, +1958 +, +1964 +; +Visser and Robinson, 1986 +), spermatozoal structure and bacular features ( +Visser and Robinson, 1987 +). Results from analysis of microcomplement fixation of albumin indicated + +A. namaquensis + +(subgenus + +Micaelamys + +) to be farther from + +A. chrysophilus + +(subgenus + +Aethomys + +) in immunological distance units than would be expected for congeneric species ( + +Watts and Baverstock, 1995 +a + +). These results were reinforced by phylogenetic analyses of mtDNA cytochrome +b +, 12S and 16S ribosomal RNA sequences, which separated + +A. namaquensis + +and + +A. chrysophilus + +into separate clades, each associated with species in other genera of the African murines sampled ( +Ducroz et al., 2001 +). A more recent phylogenetic analyses of cytochrome +b +sequences by + +Castiglia et al. (2003 +b +) + +placed + +A. chrysophilus + +and + +A. kaiseri + +in a monophyletic clade near + +Grammomys dolichurus + +in all trees but excluded + +A. namaquensis + +, associating it with either + +Lemniscomys + +or basal to members of an arvicanthine clade. We treat + +Micaelamys + +(containing + +M. granti + +and + +M. namaquensis + +) as a distinct genus: chromosomal, morphological, and molecular data clearly define it as a separate monophyletic cluster that may or may not be closely related to species of + +Aethomys + +(at least those used in the studies cited above). We also include + +Micaelamys + +with + +Aethomys + +in the same Division, but that allocation is provisional. In phylogenetic analyses of mtDNA cytochrome +b +sequences, for example, + +Aethomys + +(represented by + +A. chrysophilus + +and + +A. kaiseri + +) is closest to + +Grammomys + +, while + +Micaelamys + +( + +M. namaquensis + +) joins either + +Lemniscomys + +or is basal to an arvicanthine clade depending on the analyses ( + +Castiglia et al., 2003 +b + +; +Ducroz et al., 2001 +). Analyses of combined mtDNA cytochrome +b +, 12S and 16S ribosomal RNA sequences identified + +A. chrysophilus + +and + +G. dolichurus + +as a single clade, and placed + +M. namaquensis + +basal to that clade, a + +Dasymys +/ +Hybomys + +clade, and an arvicanthine clade ( +Ducroz et al., 2001 +). Unequivocal phylogenetic affinity of + +Aethomys + +and + +Micaelamys + +within the evolutionary radiation of African murines has yet to be uncovered, and until such resolution we isolate them in their own Division. Phylogenetic analyses employing a broader sampling of not only the speciose + +Aethomys + +but of endemic African murine genera using molecular, chromosomal, and morphological data sets may resolve the phylogenetic relationships of + +Aethomys + +and + +Micaelamys + +. Based on their results from cytochrome +b +sequences, + +Castiglia et al. (2003 +b +) + +estimated time of divergence between + +Aethomys + +(sampling + +A. chrysophilus + +and + +A. kaiseri + +) and + +Grammomys dolichurus + +as about 8 million years ago. + + +Chromosomal information available for various species (which includes those in + +Aethomys + +and + +Micaelamys +: + +Baker et al., 1988 +c + + +; + +Castiglia et al., 2003 +b + +; +Matthey, 1954 +, +1958 +, +1964 +; Viegas-Péquignot et al., 1986; +Visser and Robinson, 1986 +). +Chimimba and Dippenaar (1994) +morphometrically assessed sexual dimorphism and age variation in + +A. chrysophilus + +and + +M. namaquensis + +(the latter as + +Aethomys + +) and subsequently used statistical procedures to select the most discriminating set of morphometric characters to use in systematically revising several species of + +Aethomys +( +Chimimba and Dippenaar, 1995 +) + +. Study of the correlation between diet and molar cusp patterns in + +A. chrysophilus + +and + +M. namaquensis + +by + +Denys (1994 +a + +, the latter as + +Aethomys + +) allowed her to determine possible diets of extinct Pliocene species. Spermatozoal morphology of several species described by + +Breed (1995 +a +) + +, and used in survey of relationship among body mass, testes mass, and sperm size within murine rodents ( +Breed and Taylor, 2000 +). Morphometric and morphological definitions of southern African species, along with a taxonomic synthesis for this group of + +Aethomys + +(which included those we place in + +Micaelamys + +), provided by Chimimba (1998) and +Chimimba et al. (1999) +. Assessments of intraspecific variation and its significance in several southern African species produced by +Chimimba (2000 +, + +2001 +a + +, +b +) and +Chimimba et al. (1999) +. Evolutionary history of + +Aethomys + +(not +Micaelamy +) as documented by fossils extends back to the Pliocene and Pleistocene of East Africa ( + +Denys, 1987 +b + +, + +1994 +a + +; Jaeger, 1976; +Jaeger and Wesselman, 1976 +; +Wesselman, 1984 +), early Pliocene-late Pleistocene of +South Africa +( +Avery, 1995 +, 1998, 2000; + +Denys, 1990 +c + +), and Pleistocene of +Namibia +( +Senut et al., 1992 +); see review by Denys (1999) + +. + + + + \ No newline at end of file diff --git a/data/38/31/09/3831096783761703FF24FE24B817F446.xml b/data/38/31/09/3831096783761703FF24FE24B817F446.xml new file mode 100644 index 00000000000..f40b7271e44 --- /dev/null +++ b/data/38/31/09/3831096783761703FF24FE24B817F446.xml @@ -0,0 +1,297 @@ + + + +Salacia juradoi (Celastraceae), a new species from coastal Ecuador + + + +Author + +Cornejo, Xavier +0000-0002-4081-4047 +Herbario GUAY, Departamento de Botánica, Facultad de Ciencias Naturales, Universidad de Guayaquil, Av. Raúl Gómez Lince s. n. y Av. Juan Tanca Marengo (campus Mapasingue), P. O. Box 09 - 01 - 10634, Guayaquil, Ecuador & xcornejoguay @ gmail. com; https: // orcid. org / 0000 - 0002 - 4081 - 4047 +xcornejoguay@gmail.com + + + +Author + +Lombardi, Julio A. +Departamento de Biodiversidade, Instituto de Biociências, Universidade Estadual Paulista - UNESP, Av. 24 A, 1515, Bela Vista, 13506 - 900, Rio Claro, SP, Brazil. + +text + + +Phytotaxa + + +2021 + +2021-11-03 + + +524 + + +2 + + +125 +130 + + + +journal article +3627 +10.11646/phytotaxa.524.2.8 +0dffb7c8-328d-426a-bbc2-9fb28c92b396 +1179-3163 +5642118 + + + + + + + +Salacia juradoi +Cornejo & Lombardi + +, + +sp. nov +. + +( +Fig. 1 +). + + + + + + + +Salacia juradoi + +is a new species from coastal +Ecuador +that resembles + +S. impressifolia +(Miers.) A. C. Sm. + +, but differs by the opposite to decussate arrangement of leaves, larger leaf blades, narrowly oblong to oblong, sometimes narrowly-lanceolate, +14–30 cm +(versus elliptic, rarely ovate, obovate or lanceolate, [3.4–] +10–14.2 cm +), margin with scattered dark-brown marginal glands (vs. eglandular), flower buds oblate, light-green, white-pulverulent (versus globose, ferrugineous), margin of sepals often ciliate or ciliolate (vs. glabrate), petals patent, erose (vs. deflexed, entire), outer margin of disk entire (vs. fimbriate), and fruit with pericarp smooth (vs. verrucose). + + + + +Type: +— + +ECUADOR +. +Guayas +: +Guayaquil +, top of cerro 507, +2º09’ S +79º59’ W +, + +450 m + +, + +5 Dec 2020 + +(fl), + +X. Cornejo +& +J + + +. + +Josse 9359 +( +Holotype +: +GUAY +!) + +. + + + + +Shrubby tree to small tree 2–4(–5) m tall, to +20 cm +DBH, bark rugose, with age becoming longitudinally and irregularly fisurate. +Branches +frequently horizontally arranged, often more or less curved down, subcylindric, the terminal branchlets gray to grayish-green or the youngest full green, somewhat complanate, sometimes flexuose, minutely lenticellate, glabrous. +Stipules +deltoid to broadly deltoid, minutely ciliolate, soon deciduous, interpetiolar stipular scars present. +Leaves +opposite and decussate, sometimes subopposite, the blade coriaceous (in vivo), stiffly chartaceous (dry), usually narrowly-oblong, sometimes oblong-lanceolate or narrowly-lanceolate, 14–30 × +2.5–6 cm +, the length (3.5–)4 to 6(–6.5) times the width, the base broadly cuneate to subcordate, the margin entire, thickened, with scattered dark-brown marginal glands, the apex acute to narrowly obtuse, the adaxial side of blade deep- or olive-green, smooth, somewhat glossy, the midrib moderately prominent to impressed, yellowish to greenish for most of the length (in vivo), the blade green, smooth to subbullate, somewhat glossy (dry), the abaxial side paler green, opaque (in vivo and dry), the midrib prominent, with 7–11 secondary nerves on each side, adaxially impressed to slightly sulcate, abaxially more or less prominent (dry), glabrous, the tertiaries inconspicuous; petioles +7–16 mm +long, articulate to branch, subcylindric, thick, more or less flattened adaxially, inconspicuously rimulose, yellowish to brownish or yellowishgreen (in vivo), shallowly channelled adaxially and yellowish to gray (dry), grabrous. +Inflorescences +fasciculate, 1–4 flowers, axillary and ramiflorous; bracts inconspicuous, more or less deltoid, erose-ciliolate, reddish-brown; pedicels +10–18 mm +long, light-green, white-pulverulent. +Flower buds +oblate, light-green, white-pulverulent. +Flowers +12–15 mm +diam at anthesis, rotate; sepals deltoid to hemiorbicular, 1–2.5 × +2–3 mm +, margin often ciliate or ciliolate, lightgreen, white-pulverulent; petals suborbicular or hemiorbicular to orbicular-obovate, 4–7 × +4–7 mm +, patent at anthesis, margin erose, revolute, light-green to yellowish or light-orange, glabrous; disc patelliform, 3–5 × +1–1.5 mm +, lightgreen, the outer margin thin, light-green, cream, red to maroon or black, glabrous; stamens +1.7–2.5 mm +long, filaments linear-triangular, +1–2 mm +long, flattened, usually light-green, sometimes light-brown, anthers cordate, 0.5–1.0 mm long, 2-locular, yellow to orange; ovary +1–2 mm +diam., 3-lobed, light-green, style +0.8–1.5 mm +long, light-green, stigma not differentiated, light-green or dark-brown. +Fruit +berry, globose, 5–6 × +4.5–5.5 cm +(in vivo), green-pruinose turning to orange at maturity, epicarp coriaceous, +2–3 mm +thick (in vivo), smooth, minutely lenticellate, pedicel stout, richly lenticellate; pulp slimy, translucent, scarce; +seeds +oblong-elliptic, 1.8–2.5 × +1–1.5 cm +, surrounded by a fleshy pulp derived sarcotesta, embryo cream. + + + + +Etymology: +—The epithet honors Eduardo Jurado-Peralta ( +9 September 1969 +– +18 January 2021 +), an Ecuadorian businessman, cultural manager, and a music promoter in the city of Guayaquil, a nature lover and long-time friend of the first author, who recently passed away by Covid. + + + + +Vernacular names: +—Pomarosa de montaña ( +Clark et al. 1540 +, MO, QCNE); pomarosa de monte ( +Neill & Nuñez 10458 +, MO, QCNE). + + + + +Habitat and distribution: +— + +Salacia juradoi + +occurs on limestone rocky soils located at the narrower and altitudinally lower southeastern tip of the cordillera Chongón-Colonche, that is an extra-Andean coastal arc surrounded by highly disturbed lowland dry forests; that mountain range end up on the western side of the city of Guayaquil in coastal +Ecuador +( +Bonifaz & Cornejo 2004 +). Over +300 masl +the habitats of Chongón-Colonche turn somewhat moister refreshed by winds and cooled by microdroplets of seasonal mist ( +Fig. 2 +: A; op. cit.). The new species is restricted to secondary and mostly conserved fragments of forests often with a closed canopy between +300 to 450 masl +( +Fig. 2 +: B); for 28 years has not been observed to colonize in full sun at open cut areas nearby (Cornejo, pers. obs. in the field). The relative age of those limestone rocky soils named as San Eduardo formation where + +S. juradoi + +occurs is Middle Eocene, Lutecian to Bartonian (47.8 to 37.8 MY), those soils contain macrofossils, calcareous algae, planktonic and benthic foraminifera ( +Moreira, 2019 +). The fossil evidence suggests that those soils were shallowly sumersed as a reef within an open marine environment, and that emerged as a consequence of a colission of coastal +Ecuador +against the western Andean margin most likely during or posteriorly to the latest Oligocene-Miocene (ca. 28.1 to 20.4 MY) ( + +Jaillard +et al. +1995 + +). The new uplifted lands from Proto-Chongon-Colonche cordillera were islands that allowed the colonization most likely initially by mangrove trees that contributed at some extend on salt removal from new soils and simultaneously generating a top of organic ground, as they still do today just +3 to 5 km +south from the +type +locality, forming new soils and subsequently allowing the settlement of terra firme species and ecosystems ( +Wolf 1892 +). It is here hypothesized that spatial isolation and environmental changes drove the process of plant speciation in Proto-Chongon-Colonche islands allowing the formation of the only known population of + +S. juradoi + +, and other local and regional endemics. The berries of + +S. juradoi + +are among the largest indehicent fleshy fruits of native species in the +type +locality, as trees as + +Capparidastrum petiolare +(Kunth) Hutch. (Capparaceae) + +, and + +Gustavia angustifolia +Benth. (Lecythidaceae) + +, and vines of +Curcurbita ecuadorensis +H.C. Cutler & Whitaker ( +Cucurbitaceae +) ( +Belletini 2018 +, Cornejo obs. pers.), all of those relatively large-fruited species are dispersed by extant vertebrates and share a similar pattern of distribution that is endemic to the Pacific deciduous dry forests located in western +Ecuador +to northwestern +Peru +. + + + + +Phenology: +—Flowering from October through December, fruiting from late December through March. + + + + +Conservation status: +—The populations of + +Salacia juradoi + +occur within fragments of forests that encompasses an area of less than +75 km +2 +, that is ecologically isolated and restricted to the seasonally moister slopes and upper parts of Cerro Blanco which forms an interconnected continuum with Cerro Azul and the nearby Cerro 507, all covered by a Pacific dry deciduous seasonal native vegetation ( +Fig. 2 +). Those hills are private forests protected by the Cemento Nacional and ESPOL University that are under steady pressure by mining for cement and the expansion of urban frontier of the city of Guayaquil. Therefore, the preliminary status of EN B2 ab(iii) ( +IUCN 2017 +) is assigned to this new species. + + + + \ No newline at end of file diff --git a/data/38/31/87/383187DF7D2C4000FE3FFD0E8467FACD.xml b/data/38/31/87/383187DF7D2C4000FE3FFD0E8467FACD.xml new file mode 100644 index 00000000000..47b7a4828e3 --- /dev/null +++ b/data/38/31/87/383187DF7D2C4000FE3FFD0E8467FACD.xml @@ -0,0 +1,74 @@ + + + +The first record of Bathynellacea from Thailand: a new genus and species of Parabathynellidae (Crustacea: Syncarida) + + + +Author + +Camacho, A. I. + + + +Author + +Watiroyram, S. + + + +Author + +Brancelj, A. + +text + + +Journal of Natural History + + +2011 + +2011-12-31 + + +45 + + +45 - 46 + + +2841 +2854 + + + + +http://dx.doi.org/10.1080/00222933.2011.620715 + +journal article +10.1080/00222933.2011.620715 +1464-5262 +5204831 + + + + + + + +Siambathynella + +gen. nov. + + + + + + +Generic diagnosis + +Antennule (A.I) seven-segmented, without aesthetascs on fifth segment and with subterminal aesthetascs on last segment, sexually dimorphic, with male antennal organ on second segment of antennule. Antenna (A.II) six-segmented, first, second and fifth segments without setae. Mandible (Md) with expanded distal claw on pars molaris. Maxilla (Mx.II) with four segments. Exopod of thoracopods II–VII each two-segmented, that of Th I one-segmented; basipod of thoracopods I–VII with one smooth seta; epipod of Th I absent. Male thoracopod (Th) VIII: almost square, with small endopod integrated into basipod and with two smooth long setae; exopod, large, rectangular, twice as long as wide, overhanging basipod with three strong teeth or spinules; inner lobe incorporated into basal region, rectangular, a little shorter than dentate lobe; reduced outer lobe, fused to basipod; basipod very large, rectangular, slightly recurved and with a row of small denticles on distal part, proximal side with two lobes, one of which recurved inwards and almost completely covering the exopod, without seta. Th VIII female: triangular, with two long setae. Pleopods absent. Ventrolateral seta of pleotelson long, barbed and placed adjacent to insertion of furca. Sympod of uropod with few spines (usually eight), the distal one twice as long as rest; endopod with a spinous projection on the distal outer corner and with one strong spine ornamented with rows of setules. + + + \ No newline at end of file diff --git a/data/38/31/8B/38318B88B4C652948C60BB091C78F7BE.xml b/data/38/31/8B/38318B88B4C652948C60BB091C78F7BE.xml new file mode 100644 index 00000000000..31e80872141 --- /dev/null +++ b/data/38/31/8B/38318B88B4C652948C60BB091C78F7BE.xml @@ -0,0 +1,456 @@ + + + +The New World whirligig beetles of the genus Dineutus Macleay, 1825 (Coleoptera, Gyrinidae, Gyrininae, Dineutini) + + + +Author + +Gustafson, Grey T. +Department of Biology and Museum of Southwestern Biology, University of New Mexico, Albuquerque, NM 87131, USA +gtgustafson@gmail.com + + + +Author + +Miller, Kelly B. +Department of Biology and Museum of Southwestern Biology, University of New Mexico, Albuquerque, NM 87131, USA + +text + + +ZooKeys + + +2015 + +2015-01-23 + + +476 + + +1 +135 + + + + +http://dx.doi.org/10.3897/zookeys.476.8630 + +journal article +http://dx.doi.org/10.3897/zookeys.476.8630 +1313-2970-476-1 +086D71AF8A294F028559C2E0456B5C5B +FC4DC947FF97FF86190BFFD8B82CAB56 +578702 + + + + + +Dineutus solitarius +Aube +, 1838 + +Figures 42 +, 43 +, 46 +, 51 +, 54 + + + + +Dineutes solitarius + +Aube +1838 + +: 780, +Dineutus (Cyclinus) solitarius +: +Hatch 1925b +: 137, + +Dineutus solitarius + +: +Leech 1940 +: 74, +Dineutus (Cyclinus) solitarius +: +Leech 1948 +: 422, + +Dineutus solitarius + +: + +Arce-Perez +and Roughley 1999 + +: 84. + + + +Type locality. +Mexico, Veracruz + + +Specimens examined. +87 + + +Type material examined. + +Lectotype, here designated (1 ♂ male pinned) "MUSEUM PARIS/ VERA-CRUZ/ 1833 [beige label, typed black ink]// green disc [underneath is handwritten Veracruz/ 1883// in black ink]// + +solitarius + +[beige label, handwritten in black ink, handwriting appears to be +Aube's +]// TYPE [white label, typed red ink]// LECTOTYPE [red label, typed black ink]//" deposited in the MNHN. + + + +Material examined. + +COSTA RICA: +Guanacaste: +Santa Rosa N.P., +10°50.35'N +, +85°37.07'W +, 300 m, 6.vi.2008, leg. E. Nearns, I. Swift (2 ex. MSBA); 0.25km S Santa Rosa N.P., roadside pool, 15.vi.2003, leg. W.D. Shepard, EMEC 204684-204687; EMEC 204675 (5 ex. EMEC); La Pacifica nr Canas, 8.vi.1983, leg. J.E. Wappes, (1 ex. FSCA). +EL SALVADOR: +La Libertad: +Hacienda Capolinas, 5 km NW Quezaltepeque, 455 m, 21.xii.1964, leg. M.E. Irwin (1 ex. UCRC). +GUATEMALA: +Jalapa: +4-7 km E. Jalapa, 12.vi.1991, leg. J.E. Wappes (1 ex. FSCA). +HONDURAS: +Comayagua: +Malootal Minas de Oro, v.1932, leg. J.B. Edwards (3 ex. KSEM); + +Francisco +Morazan +: + +4.5 km S.E. El Zamorano, 25.iv.1993, leg. I. Stange & R. Miller (1 ex. FSCA); +La Paz: +La Paz, 21.vii.1978, leg. V. Diaz, EMEC 204672 (1 ex. EMEC). +MEXICO: +Chiapas: +2.7mi W Colonia, Lazaro Cardenas, 6.viii.1965, leg. J.D. McCarty, EMEC 654699; EMEC 204761; EMEC 204769; EMEC 204777; EMEC 204801; EMEC 204807-204809 (8 ex. EMEC); 20 mi W of Cintalapa, 31.xii.1955, leg. J.C. Schaffner (2 ex. FSCA); +Guerrero: +Rincon, "kil.-256 S. MexCity", 31.x.1936, leg. H.D. Thomas (1 ex. KSEM); +Jalisco: +UNAM Biol. Sta. Chamela, 61 m, 9.viii.1982, leg. C.W. & L. +O'Brien +& G. Wibmer, at light (1 ex. FSCA); Est. Biol. Chamela, at lites, 13-22.vii.1992, leg. J. Chemsak, EMEC 204753; EMEC 204881; EMEC 204897; EMEC 204925 (4 ex. EMEC); 20 mi N Puerto Vallerta, +"200" +, 29.viii.1971, leg. J. Cicero (1 ex. FSCA); +Nayarit: +7 mi. N Tetitlan, 14.vi.1962, leg. D.H. Janzen, EMEC 204772-204773; EMEC 204786; EMEC 204800; EMEC 204805-204806; EMEC 204857-204858; EMEC 204917-204920 (11 ex. EMEC); El Pichon, 25.vi.1963 (1 ex. FSCA); Jesus Maria, 26.vi.1955, leg. B. Malkin, EMEC 204804 (1 ex. EMEC); Sierra Zapotan, 1300 m, iii.1943, leg. E. Paredes (3 ex. UCRC); 24 mi SE Tepic, 1045 m, 22.vi.1968, leg. A.R. Hardy, L. Espinosa, J.P. Abrayaya (2 ex. UCRC); 20.3 mi W Compostela, 60 m, 19.vi.1967, leg. A.R. Hardy (1 ex. UCRC); + +Nuevo +Leon +: + +10km N Linares, mercury vapor lamp, 430 m, 23.iii.1991, leg. R. Brooks, R. Leschen, Coll. No. 58 (1 ex. KSEM); +Oaxaca: +5 mi N La Ventosa, 4.vii.1970, leg. R.E. Beer & party (3 ex. KSEM); 80km N of Arriga,10.vi.1971, leg. S.R. & L.M. Steinhauser (2 ex. FSCA); +Quintana Roo: +10.9km S Playa del Carmen,1.vii.1990, leg. M.C. Thomas, (1 ex. FSCA); Isla de Cozumel, SW side 2mi W Cedral, 8.x.1993, leg. C.B. Barr & W.D. Shepard, EMEC 654700 (1 ex. EMEC); + +San Luis +Potosi +: + +El Salto Falls, 15.vi.1956, leg. R.E. Beer & party (5 ex. KSEM); El Salto, 19.vi.1953, Univ. Kans. Mex. Expedition (2 ex. KSEM); same as previous except: 488 m, 24.viii.1954 (1 ex. KSEM); same as previous except: 381 m, 4.ix.1962, leg. Ordway & Marston, at light (1 ex. KSEM); +Sinaloa: +Culiaoan, 6 mi S, Black & White lights, 6.viii.1964, leg. J.A. Chemsak & J. Powell, EMEC 204803 (1 ex. EMEC); 5 mi N Mazatlan, at light, 11.x.1975, leg. J. Powell, J. Chemsak, T. Friedlander, EMEC 204778 (1 ex. EMEC); 15 mi SE Mazatlan, 27.vii.1973, leg. J. Chemsak, E.G. Linsleys & A.E. Michelbacher, EMEC 204779 (1 ex. EMEC); +Veracruz: +15mi NW of Acayucan, 18.vi.1958, leg. J.C. Schaffner, (1 ex. FSCA); Palma Sola, "255 Pastizal", 23.viii.1973, leg. G. Halffter & P. Reyes, Blacklight trap (1 ex. FSCA); 6mi SE Rinconada, 21.vi.1962, leg. D.H. Janzen, EMEC 204921 (1 ex. EMEC). +NICARAGUA: +Rivas: +E of Lago de +Apanas +, +13°12.77'N +, +86°58.06'W +, 966 m, 12.vi.2005, leg. W.D. Shepard, EMEC 204676-204683 (8 ex. EMEC); +Jinotega: +roadside pool, Lago de +Apanas +area, N Jinotega, +13°12.8'N +, +85°58.1'W +, 966 m, 12.vi.2005, leg. C.B. Barr, EMEC 204673-204674 (2 ex. EMEC). +U.S.A.: +California: +Riverside Co., Mecca, 15.viii.1924, EMEC 654698 (1 ex. EMEC); +Texas: +"Pinto" +, 7.vii.1938, leg. D. W. Craik (1 ex. KSEM). + + + +Diagnosis. + +Male (Fig. +42C-D +): Size: 9.2-10.4 mm. Body form broadly oval; elytral apices regularly broadly rounded, with serrations and irregularities absent apically, elytra reticulation normally coarse and well impressed laterally, medially being replaced by fine microreticulation, elytral disc medially often with fine and weakly impressed punctures, striae very faintly present, most evident medially on elytral disc; profemora with small sub-apicoventral tooth atop profemoral carina; protibiae weakly subsinuate to club-shaped; mesotarsal claws (Fig. +43C +) with ventral margin straight, with weak medial expansion; venter darkly colored, usually black to very dark reddish brown, mesothoracic and metathoracic legs usually lighter in coloration, as well as apex of abdomen; Aedeagus (Fig. +43A, B, D +) median lobe in dorsal view just shorter than parameres, mildly parallel sided, weakly angled towards apex, acuminate in apical 1/5, apical median lobe angled towards acumination, lateral margins of acumination angled toward apex, apex very shortly rounded producing a strong point, in lateral view median lobe evenly shallowly curved dorsally, ventrally median lobe with diamond shaped sperm-groove, parameres in dorsal view weakly expanded laterally at apical 1/3, narrowly rounded apically. + + +Female (Fig. +42A-B +): Size: 9.1-10.2 mm. Body form regularly oval; elytral apices regularly broadly rounded, with serrations and irregularities absent apically, apicolateral sinuation absent, elytra reticulation course and well impressed laterally, medially being replaced by fine microreticulation, elytral disc medially often with fine and weakly impressed punctures, striae very faintly present, most evident medially on elytral disc; profemora without sub-apicoventral tooth; protibiae club-shaped; venter darkly colored, usually black to very dark brown, mesothoracic and metathoracic legs usually lighter in coloration, as well as apex of abdomen. + + + +Figure 42. + +Dineutus solitarius + +. +A +♀ dorsal habitus +B +♀ ventral habitus +C +♂ dorsal habitus +D +♂ ventral habitus. All scale bars ≈ 2 mm. + + + + +Figure 43. + +Dineutus solitarius + +. +A +aedeagus dorsal view +B +aedeagus ventral view +C +♂ mesotarsal claws +D +aedeagus lateral view. Scale bar for +C +≈ 0.10 mm all others ≈ 1 mm. + + + + +Differential diagnosis. + + + +Dineutus +solitarius + + +is unique among all other North American + +Dineutus + +in being smaller in size (9.1-10.4 mm), with a broadly oval body form (Fig. +42C +), having the elytral apices broadly rounded without serrations and/or irregularities, males with the profemoral sub-apical ventral tooth small and atop a carina, and by the form of the aedeagus (Fig. +43A +). The species most similar to + +Dineutus solitarius + +are + +Dineutus carolinus + +and + +Dineutus emarginatus + +. Both sexes of + +Dineutus solitarius + +can be distinguished from + +Dineutus carolinus + +in having the elytral apices broadly rounded without apical serrations and/or irregularities, as opposed to having the elytral apices narrowly rounded with serrations and/or irregularities present. The body form of + +Dineutus solitarius + +is much more regularly oval as opposed to being more elongate overall in + +Dineutus carolinus + +. + +Dineutus solitarius + +lacks a defined lateral marginal depression as seen in + +Dineutus carolinus + +as a result of being more dorsoventrally convex. + + +Of the two species similar to + +Dineutus solitarius + +, + +Dineutus emarginatus + +is more similar, in that both of these species have the elytral apices fairly broadly rounded and without apical serrations and/or irregularities present. Furthermore, the aedeagi of these two species are somewhat similar both being acuminate. In general both sexes of + +Dineutus solitarius + +can be distinguished from + +Dineutus emarginatus + +in being much more regularly rounded in body form than + +Dineutus emarginatus + +, whose body form is more elongate oval. The pronotal shape of the two species differs fairly noticeably, in + +Dineutus solitarius + +the pronotum has the lateral borders much more obtusely angled posteriorly to anteriorly, and the posterior margin of the pronotum flatly meets the posterolateral corners of the pronotum, while in + +Dineutus emarginatus + +the pronotum has the lateral borders more straightly angled posteriorly to anteriorly with the posterior margin being more sinuate. + + +Males of + +Dineutus solitarius + +can further be removed from + +Dineutus emarginatus + +in having a small profemoral sub-apicoventral tooth atop a carina, while in + +Dineutus emarginatus + +the tooth is much more large and triangular. The aedeagi of these two species are similar in that both have an acuminate median lobe, however the general shape of the median lobe of the two aedeagi can be separated without difficulty. The median lob of + +Dineutus solitarius + +(Fig. +43A +) is much more parallel sided, being weakly narrowed towards the acumination and the acumination itself having its margins angled towards the apex, which is very narrowly rounded giving it a very pointed feel. In + +Dineutus emarginatus + +the median lobe (Fig. +20A +) is weakly constricted medially giving the lateral margins a slight sinuation, the apical margins of the median lobe are rounded towards the acumination, with the acumination having its lateral margins fairly straight, and the apex relatively more broadly rounded, giving it a more rounded pointed shape, as opposed to narrowly pointed as in + +Dineutus solitarius + +. + + +The females of + +Dineutus solitarius + +differ primarily in the general differences between the two species. + + + +Distribution + + +(Fig. +54B +). + +From extreme southern United States, Texas ("Pinto Texas" 1938 [KSEM]) and California ( +Leech 1940 +; +Leech 1948 +), throughout Mexico ( +Ochs 1949 +) and Central America to western Costa Rica. The first author visited the only known California locality, the city of Mecca, in Riverside County, in southwestern California, in the summer of 2012, in an attempt to recollect this species. The area had changed quite a bit with much of the duck ponds in the area having dried up and an increased agricultural presence was evident. + + + +Habitat. +This species appears to be lotic. Several locality labels list "pools in stream". In La Selva Negra, Nicaragua, specimens were collected from a pool within a stream by the second author. + + + +Discussion +. + + +It should be noted that + +Dineutus solitarius + +is primarily a Mexican and Central American species, only just barely reaching the United States. Historical records indicate it was at one point found in California ( +Leech 1940 +) and Texas. + + +There is some noticeable variation in the elytral sculpturing among populations of + +Dineutus solitarius + +. Specimens from Sierra de Zapotan, Nayarit, Mexico (UCRC) have the punctures of the elytra much more shallowly and weakly impressed, making them much larger and +"dimply" +in appearance (Fig. +46B +). This is most noticeable medially on the elytra discs near the sutural region, where the strong lateral reticulation is replaced by the fine mesh microreticulation. Interestingly a similar situation is seen in specimens from the same area of + +Dineutus sublineatus + +(Fig. +46A +). These specimens with the dimply punctation make it apparent that the fine weakly impressed punctation seen normally medially on the elytral discs is also present laterally, but is obscured by the strong reticulation of that area, and is visible medially and suturally due to the fine microreticulation of that area. Specimens from Costa Rica (MSBA) also show variation in elytral sculpturing, having the reticulation of the elytra composed of much finer meshes. The lateral meshes are still stronger but not nearly as coarse as in other populations. Specimens of + +Dineutus solitarius + +from Oaxaca, Mexico, near Arriba, (FSCA) show variation in body form. The outline of the body is much more broadly oval in these specimens. There is also a much greater dorsoventral convexity in the scutellar region, especially evident in lateral view. It should be noted that although there are these variations among populations, the aedeagi of males from each of these populations are not noticeably different or variable in any significant manner. + + + +Type designation. + +Similar to the situation with + +Dineutes metallicus + +Aube +, the only specimen with a date and +Aube's +handwriting for the determination label was selected as the lectotype (Fig. +51C +). The other specimens in the MNHN collection lacked dates and/or +Aube's +handwriting, therefore we did not designate paralectotypes. + + + + \ No newline at end of file diff --git a/data/38/31/DA/3831DA62D6F21DEAE26A703B5EB5F842.xml b/data/38/31/DA/3831DA62D6F21DEAE26A703B5EB5F842.xml new file mode 100644 index 00000000000..159db99436d --- /dev/null +++ b/data/38/31/DA/3831DA62D6F21DEAE26A703B5EB5F842.xml @@ -0,0 +1,307 @@ + + + +Mexistenasellusfloridensis sp. n., the first stenasellid isopod discovered from the Floridan aquifer (Crustacea, Isopoda, Asellota) + + + +Author + +Lewis, Julian J. + + + +Author + +Sawicki, Thomas R. + +text + + +Subterranean Biology + + +2016 + +17 + + +121 +132 + + + + +http://dx.doi.org/10.3897/subtbiol.17.7703 + +journal article +http://dx.doi.org/10.3897/subtbiol.17.7703 +1314-2615-17-121 +B3F7DFEBB1194A72848A5924BD337CEE + + + +Taxon classification Animalia Isopoda Stenasellidae + + + +Mexistenasellus floridensis +sp. n. +Figures 1, 2, 3, 4, 5 + + + +Material examined. + +USA: FLORIDA: Jackson County, Hole in Wall Cave, approximately 7 km east of Marianna ( +N30.78334 +W85.15671 +), male holotype, 3 male and 2 female paratypes, collected 19 October 2013, Thomas R. Sawicki and Michael Stine; same locality, 3 male and 1 female paratypes, 2-3 January 2009, Thomas R. Sawicki. The specimens are deposited in the collection of the US National Museum of Natural History, Smithsonian Institution, Washington, D.C. + + + +Description. + +Eyeless, unpigmented, longest male approximately 9.0 mm, female 9.4 mm. Body slender, linear, about 4.3 +x +as long as wide. Head about 1.4 +x +as wide as long, rostrum and lateral incisions absent. Coxae not visible in dorsal view. Body becoming more dorsally spinose on pereonites 6-7 and pleon. Pleotelson about 1.65 +x +as long as wide, caudomedial lobe moderately produced, broadly rounded. + + +Antenna 1 of 20 articles, distal 6 articles each with one esthete, then alternate articles with one esthete (8 esthetes total). Antenna 2 broken or detached in most specimens, flagellum 57-58 merous, esthetes absent. Mandibles with 4-cuspate incisors +and +lacinia; spine row with 5 spines on left, 4 spines on right, both with simple stout spines adjacent to incisors that resemble the cusps of the incisors and spines distad from incisors with complex plumosity; left molar with row of 15 plumose setae, right molar with row of 12 plumose setae. Mandibular palp 3-merous, with plumose setae on distal articles. Maxilla 1, inner lobe with 4 apical stout plumose spines; outer lobe with 12 dentate apical spines. Maxilliped without retinaculae. + + +Pereopods with sexual dimorphism not apparent. Pereopod 1, dactyl with elongate spine resembling accessory claw, 0.8 +x +length of claw; propodus about 2.1 +x +as long as +wide +, palmar margin with 4-6 robust plumose spines; carpus with 3-4 spines continuing from propodus. Pereopods 2-7 increasing in length, pereopod 7 longest; dactyls with prominent elongate claw-like spine parallel to claw. + + +Male pleopod 1, protopod with retinaculae absent; exopod oval with 5 elongate disto-lateral setae. Female pleopod 2 triangular, about 2.1 +x +as long as wide, with 3 setae +inside +mesial margin, 1 distal seta and 1 lateral seta at mid-point. Male pleopod 2, protopod elongate, about 1.7 +x +as long as wide; exopod, proximal article sub-equal in length to distal article, setae absent, distal article broadly rounded apically, with 5 lateral setae; endopod, setation absent, distal article about 2 +x +length of proximal article, bent at approximately 60 degree angle to proximal article, tip bi-lobed, separated by endopodial groove terminating in sub-conical stylet (cannula). Pleopod 3, exopod with transverse suture, distal area slightly longer than proximal, with submarginal spines in row along mesial margin, spines and setae along distal and lateral margins; endopod about 0.6 +x +length of exopod, bifurcated distally. Pleopod 4, exopod with oblique suture, about 2.5 +x +as long as wide, area distal to suture about 0.67 +x +length of proximal area, with about 32 marginal setae; endopod about 0.6 +x +length of exopod, bifurcated distally. Pleopod 5, exopod with oblique suture, setae absent, about 2.5 +x +as long as wide, area distal to suture about 0.3 +x +length of proximal area; endopod sub-equal in length to exopod, bifurcated distally. + + +Uropods about 2.4mm in length, equal to pleotelson; rami slender, linear, endopod 5 +x +length of protopod, 1.25 +x +length of exopod. + + + +Etymology. +Named for the state of Florida, in recognition of the first stenasellid discovered in the United States east of the Mississippi. Suggested vernacular name is the Florida cave isopod. + + +Relationships. + +Magniez (1981) +believed that the North American stenasellidae would prove to be multi-generic, although the paucity of collections has so far supported the partitioning of the New World taxa into only two genera ( +Magniez 1999 +; +2008 +). Within the genus +Mexistenasellus +, +Mexistenasellus floridensis +seems to most closely resemble +Mexistenasellus coahuila +and +Mexistenasellus colei +. The male pleopod 2 endopodite of all three species is an elongate, sub-rectangular structure terminating in a short stylet that is presumably the sperm transfer cannula, surrounded by the rounded terminal lobes of the endopodial groove. The exopod of each is divided by a suture into two sub-equal parts, with sparse setation along the distal margin. The first maxilla of all three species also share an inner lobe with 4 setae and outer lobe with 12 apical spines. + + +Nearctic +Mexistenasellus +species can be tentatively identified by their ranges (Fig. 1). From a morphological standpoint, +Mexistenasellus floridensis +is separated from the most similar species ( +Mexistenasellus colei +, +Mexistenasellus coahuila +) by the structures of the male second pleopod, namely the more slender, elongate endopodite and the presence of five setae along the margin of the exopod, as compared to one seta in the other species. Other unique morphological aspects of +Mexistenasellus floridensis +include the absence of retinaculae on the maxilliped and the distally bifurcate endopods of pleopods 3-5. + + +When +Cole and Minckley (1972) +described the first stenasellid discovered in the Nearctic Region they noted the morphological resemblance between +Mexistenasellus coahuila +in northeastern Mexico and +Parastenasellus +from northern Africa. +Magniez (1981) +concurred with Cole and +Minckleys' +observation, and further compared the morphology of +Mexistenasellus coahuila +with the African stenasellid genera +Parastenasellus +, +Magniezia +and +Metastenasellus +. The male second pleopods of all of these genera are similar, excluding +Metastenasellus +, which possesses a spiraled-appearing endopodite that is quite dissimilar. + + +The hypothesis of Magniez entails colonization of groundwater by the stenasellid ancestors prior to the separation of Africa and South America during the early +Cretaceous +(140-150 million years before present). This idea requires the presence of stenasellids in South America that remain to be discovered, and subsequent dispersal to North America during the Cenozoic. Magniez acknowledged the flaw in the hypothesis presented by the fact that the North and South American continents were separated during the majority of the Cenozoic. This problem is avoided by pushing back the invasion of freshwater habitats by stenasellids even further, to a time prior to the rifting of Pangea during the Jurassic (about 175 million years b.p.). + + +The +molecular genetic analysis of stenasellids by +Morvan et al. (2013) +supports the hypothesis that stenaselllids were present on Pangaea. Their data indicates that +Mexistenasellus +and +Magniezia +are sister groups and form a group separate from +Stenasellus +, with divergence possibly dating to the late Paleozoic. If one assumes that the African precursors were present prior to the breakup of Pangea, the theoretical presence of stenasellids in South America is no longer necessary. On the other hand, the molecular data do not support the argument of +Bowman (1982) +that supposed the invasion of groundwater in Mexico by the marine ancestors of +Mexistenasellus +as the shallow marine embayment regressed during the early Cenozoic. + + + +Ecology. + +The Hole in Wall Cave is a water-filled cave system that is a popular dive site located in +Merritt's +Mill Pond, east of Mariana, Florida. The cave was mapped by +Exley (1978) +with the current surveyed length of approximately 8.5 km and maximum depth of 42.3 m. The isopods were collected as they swam, mid-water, at an average depth of approximately 24 m. + + +This observation of the isopods swimming is curious since the pereopods of +Mexistenasellus floridensis +do not exhibit the dense rows of setae present on the legs of +Remasellus parvus +that appear to be natatory adaptations. Regardless of how ill-prepared the isopods were for swimming that was precisely what they appeared to be doing each time specimens were collected. The asellid +Caecidotea putea +Lewis (2009) +was also present in the water column with +Mexistenasellus floridensis +. This isopod seems no more morphologically adapted for swimming than the stenasellid. + + +On 17 July 2015 and 31 July 2015, dives were conducted in Hole in the Wall Cave to conduct careful behavioral observations of the isopods as well as to collect physicochemical data from the cave and surface pond. During these dives isopods were observed crawling on the floor, walls, and ceiling of the cave, as well as swimming in the water column. The swimming behavior observed in these animals may be in response to physical disturbance. This hypothesis is based on the fact that isopod swimming behavior was observed more frequently by the second diver than the lead diver as the team swam through the cave. Both +Mexistenasellus floridensis +and +Caecidotea putea +exhibited a fluid, graceful swimming motion. This fact at least suggests that although fin kicks and bubbles exhaled from SCUBA equipment may have induced their movement, it is not an unfamiliar, artificial behavior. It is easier to visually spot the isopods as they swim in the water column, where their unpigmented bodies are set against the dark cave background, than against the white limestone walls and ceilings or the silt-covered bottom. Due to this fact divers were focused on collecting animals that were swimming in the water column, and therefore likely missed many isopods that may have been crawling on surfaces within the cave. In total, these facts may explain why animals, seemingly poorly adapted for swimming, were collected solely from the mid-water column. + + +This swimming behavior may be an adaptive flight response to escape predation from the crayfish +Cambarus cryptodytes +, the Georgia cave salamander +Eurycea wallacei +or the trogloxene yellow bullhead catfish +Ameiurus natalis +. Other members of the community, a subset of the Florida subterranean fauna discussed by +Franz et al. (1994) +, +were +the stygophilic amphipod +Crangonyx floridanus +and other (probably undescribed) stygobitic amphipods. + + +During the 31 July 2015 dive, physicochemical data was taken using a Hydrolab HL4 sonde. Readings of depth, temperature, pH, conductivity, and dissolved oxygen (DO) were recorded every 20 seconds continuously during the dive. Dive bottom time (time spent swimming through cave passages and not entering and exiting the cave) was 51 minutes, and 155 separate readings were taken with depth varying between 19.57 and 31.53 meters. Readings were also taken in the open water of +Merritt's +Mill Pond. For each parameter measured, the shallowest regions of the cave most closely approximated the pond water; however, temperature, pH, and DO progressively decreased with depth and specific conductivity increased with depth (Table 1). The lowest temperature, pH and DO, and highest conductivity were measured below 31 meters. The cold, low DO, high conductivity water entered the main cave passage from deep side tunnels at approximately 600 meters from the cave entrance. One of us (TRS) has explored these cave passages for the past six years and has noted seasonal variation in cave water temperature at depths between 19 and 30 meters. In total, these data suggest that the cold water entering the primary passage comes from deep water sources, less influenced by seasonal variation. While no isopods were observed in this colder water, stygobitic amphipods were collected. + + + +Table 1. Physicochemical data correlated with depth. The 2 m reading was outside of the cave in the open water of +Merritt's +Mill Pond. The deepest sections of the cave correlated with the lowest temperature, pH, and DO, and highest specific conductivity. + + + + + + + + + + + + + + + +
Depth mTemperature °CpHDissolved Oxygen +Conductivity +µS +/cm +
mg/l% Saturation
+
+ +Concerning reproduction, a 7.4 mm female +Mexistenasellus floridensis +was ovigerous with a brood pouch containing eggs approximately 0.5 mm in diameter. Another post-ovigerous female released 32 juveniles about 1.4 mm in length. + + + +Figure 2. +Mexistenasellus floridensis +sp. n., male: a habitus b head, antenna 1, antenna 2 peduncle c uropod. + + + + +Figure 3. +Mexistenasellus floridensis +sp. n., mouthparts: a maxilla 1 b mandible, right, incisors c mandible, left, incisors and lacinia d mandibular palp e maxilliped. + + + + +Figure 4. +Mexistenasellus floridensis +sp. n., pereopods: a pereopod 1 distal articles, female b spine, pereopod 1, palmar margin of proprodus c pereopod 7, male d same, dactyl. + + + + +Figure 5. +Mexistenasellus floridensis +sp. n. pleopods, male except 4e: a pleopod 1 b pleopod 2 c same, tip of endopodite, anterior d same, posterior e pleopod 2 f pleopod 3 g pleopod 4 h pleopod 5. + + +
+
+
\ No newline at end of file diff --git a/data/38/32/0C/38320CDE73D26F5F62338D92DDFA5ABE.xml b/data/38/32/0C/38320CDE73D26F5F62338D92DDFA5ABE.xml new file mode 100644 index 00000000000..803d6c64bd6 --- /dev/null +++ b/data/38/32/0C/38320CDE73D26F5F62338D92DDFA5ABE.xml @@ -0,0 +1,98 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part C) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +370 +473 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Crotalaria sessiliflora +Linnaeus + +, + +Species Plantarum +, ed. 2, 2 + +: 1004. 1763 + + +. + + + +"Habitat in China." RCN: 5254. + + + + +Neotype +(Niyomdham in +Thai Forest Bull., Bot. +11: 153. 1978): Herb. Linn. No. 895.9 ( +LINN +) + +. + + + + +Current name: + + +Crotalaria sessiliflora + +L. + +( +Fabaceae +: +Faboideae +). + + + + +Note: +Niyomdham wrongly indicated 895.9 (LINN) as the +holotype +(it is not original material for the name). However, in the absence of any original material, this is accepted as a neotypification under Art. 9.8. + + + + \ No newline at end of file diff --git a/data/38/32/0F/38320FF1113F94A6B649E638A8AD1F87.xml b/data/38/32/0F/38320FF1113F94A6B649E638A8AD1F87.xml new file mode 100644 index 00000000000..db855638995 --- /dev/null +++ b/data/38/32/0F/38320FF1113F94A6B649E638A8AD1F87.xml @@ -0,0 +1,46 @@ + + + +Die Milbenfauna der Nordseeinsel Wangerooge + + + +Author + +Willmann, C. + +text + + +Veröffentlichungen des Instituts für Meeresforschung Bremerhaven + + +1952 + +1 + + +139 +186 + + + + +http://unknown + +journal article +ORI11037 + + + + +21. +Rhombognathus spinipes Viets +. + + + +a. Adultus dorsal, b. Bein I, c. Adultus ventral. + + + \ No newline at end of file diff --git a/data/38/32/47/3832476E5A0F523CA9FDEFBF5381A5D8.xml b/data/38/32/47/3832476E5A0F523CA9FDEFBF5381A5D8.xml new file mode 100644 index 00000000000..b34c6089e48 --- /dev/null +++ b/data/38/32/47/3832476E5A0F523CA9FDEFBF5381A5D8.xml @@ -0,0 +1,78 @@ + + + +Integrative taxonomic revision of the genera Nesticella and Howaia in Japan with the description of five new species (Araneae, Nesticidae, Nesticellini) + + + +Author + +Ballarin, Francesco +https://orcid.org/0000-0003-1417-2519 +Systematic Zoology Laboratory, Department of Biological Sciences, Tokyo Metropolitan University, 1 - 1 Minami-Osawa, Hachioji-shi, 192 - 0397, Tokyo, Japan & Department of Zoology, Museo di Storia Naturale of Verona, Lungadige Porta Vittoria, 9, I- 37129 Verona, Italy +ballarin.francesco@gmail.com + + + +Author + +Eguchi, Katsuyuki +https://orcid.org/0000-0002-1054-1295 +Systematic Zoology Laboratory, Department of Biological Sciences, Tokyo Metropolitan University, 1 - 1 Minami-Osawa, Hachioji-shi, 192 - 0397, Tokyo, Japan & Department of International Health and Medical Anthropology, Institute of Tropical Medicine, Nagasaki University, 1 - 12 - 4 Sakamoto, Nagasaki-shi, 852 - 8523, Nagasaki, Japan + +text + + +ZooKeys + + +2023 + +2023-08-11 + + +1174 + + +219 +272 + + + + +http://dx.doi.org/10.3897/zookeys.1174.101251 + +journal article +http://dx.doi.org/10.3897/zookeys.1174.101251 +1313-2970-1174-219 +608FAD80206A428E9743F8ED4F3139BB +D0C94D1974975A4B9CD9EE6F18A21120 + + + + +Gen. +Howaia Lehtinen & Saaristo, 1980 + + + + +Nesticella mogera += +N. mogera +group sensu +Lin et al. 2016 +. + + + +Type species. + + +Nesticus mogera + +Yaginuma, 1972 from Japan. + + + + \ No newline at end of file diff --git a/data/38/32/50/383250A947566F61A27BF80E172F0FC6.xml b/data/38/32/50/383250A947566F61A27BF80E172F0FC6.xml new file mode 100644 index 00000000000..9e53e7c6ec7 --- /dev/null +++ b/data/38/32/50/383250A947566F61A27BF80E172F0FC6.xml @@ -0,0 +1,74 @@ + + + +Guide to the Vascular Flora of the Savannas and Flatwoods of Shaken Creek Preserve and Vicinity (Pender & Onslow Counties, North Carolina, U. S. A.) + + + +Author + +Thornhill, Robert + + + +Author + +Krings, Alexander + + + +Author + +Lindbo, David + + + +Author + +Stucky, Jon + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1099 +1099 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1099 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1099 +1314-2828-2-1099 + + + + +Campsis radicans (L.) Seem. ex Bureau + + + +Distribution +Margins of wet pine flatwoods (WPF-T) and adjacent swamps. + + +Notes + +Infrequent. +Jun-Jul +; +Sep-Oct +. Thornhill 1482 (NCSC). Specimens seen in the vicinity: Sandy Run [Hancock]: Taggart SARU 198 (WNC!). [= RAB, Weakley] + + + + \ No newline at end of file diff --git a/data/38/32/87/383287CC0350FFA58E91FC5B536BFA33.xml b/data/38/32/87/383287CC0350FFA58E91FC5B536BFA33.xml new file mode 100644 index 00000000000..5f8fc84dab9 --- /dev/null +++ b/data/38/32/87/383287CC0350FFA58E91FC5B536BFA33.xml @@ -0,0 +1,125 @@ + + + +Two new species of Eupalopsellidae (Acari: Prostigmata: Raphignathoidea) and key to the world species of Exothorhis Summers + + + +Author + +Khan, Eid Muhammad + + + +Author + +Kamran, Muhammad + + + +Author + +Rehman, Muneeb Ur + + + +Author + +Mirza, Jawwad Hassan + + + +Author + +Alatawi, Fahad Jaber + +text + + +Journal of Natural History + + +2024 + +2024-05-16 + + +58 + + +13 - 16 + + +511 +526 + + + +journal article +10.1080/00222933.2024.2331825 +1464-5262 +11239904 + + + + + + + +Exothorhis justicia +Roy, Gupta and Saha + +species inquirenda + + + + + + + + + +Exothorhis justicia +Roy, Gupta and Saha, 2006: 307 + + + + + + + +Remarks + + + +Exothorhis justicia + +was described from only +one female +and differentiated from the male of + +E. nadiaensis + +(female unknown) by differences in distances and shape of dorsal body setae and leg tarsal claws. This species was illustrated having one more dorsal body seta ( + +c +3 + +) which is not characteristic for the genus + +Exothorhis + +(13 pairs of opisthosomal dorsal setae present in all + +Exothorhis +species + +). Therefore, the identity of this species is considered a uncertain and doubtful. Hence, + +E. justicia + +is suggested as species inquirenda. + + + + \ No newline at end of file diff --git a/data/38/32/87/383287CC0350FFA58E91FD27536FFC7C.xml b/data/38/32/87/383287CC0350FFA58E91FD27536FFC7C.xml new file mode 100644 index 00000000000..3b776887741 --- /dev/null +++ b/data/38/32/87/383287CC0350FFA58E91FD27536FFC7C.xml @@ -0,0 +1,109 @@ + + + +Two new species of Eupalopsellidae (Acari: Prostigmata: Raphignathoidea) and key to the world species of Exothorhis Summers + + + +Author + +Khan, Eid Muhammad + + + +Author + +Kamran, Muhammad + + + +Author + +Rehman, Muneeb Ur + + + +Author + +Mirza, Jawwad Hassan + + + +Author + +Alatawi, Fahad Jaber + +text + + +Journal of Natural History + + +2024 + +2024-05-16 + + +58 + + +13 - 16 + + +511 +526 + + + +journal article +10.1080/00222933.2024.2331825 +1464-5262 +11239904 + + + + + + + +Exothorhis nadiaensis +Chatterjee and Gupta + +species inquirenda + + + + + + + + +Exothorhis nadiaensis +Chatterjee and Gupta + +, in + +Gupta 2002: 93 + + + + + + +Remarks + + + +Exothorhis nadiaensis + +was described from only +one male +specimen and differentiated from the female of + +Raphignathus costatus + +by relative length of dorsal body setae, chaetotaxy of legs and striations pattern on stylophore. The diagnosis of this species has been ambiguous and indistinct. Therefore, the identity of this species is uncertain and doubtful, and it is considered a species inquirenda. + + + + \ No newline at end of file diff --git a/data/38/32/87/383287CC0350FFA58E91FF5C536AFDDB.xml b/data/38/32/87/383287CC0350FFA58E91FF5C536AFDDB.xml new file mode 100644 index 00000000000..ce85ae39cf9 --- /dev/null +++ b/data/38/32/87/383287CC0350FFA58E91FF5C536AFDDB.xml @@ -0,0 +1,132 @@ + + + +Two new species of Eupalopsellidae (Acari: Prostigmata: Raphignathoidea) and key to the world species of Exothorhis Summers + + + +Author + +Khan, Eid Muhammad + + + +Author + +Kamran, Muhammad + + + +Author + +Rehman, Muneeb Ur + + + +Author + +Mirza, Jawwad Hassan + + + +Author + +Alatawi, Fahad Jaber + +text + + +Journal of Natural History + + +2024 + +2024-05-16 + + +58 + + +13 - 16 + + +511 +526 + + + +journal article +10.1080/00222933.2024.2331825 +1464-5262 +11239904 + + + + + + + +Exothorhis eorhis +Rimando and Corpuz-Raros + +species inquirenda + + + + + + + +Exothorhis eorhis +Rimando and Corpuz-Raros, 1996: 114 + + + + + +Remarks + + + +Exothorhis eorhis + +was described only from +two male +specimens, each were collected from different localities and hosts. This species was differentiated from the deutonymph of + +E. phoenixi + +and male of + +E. bixae +Rimando and Corpuz-Raros + +by having smooth anogential setae ( + +g +1 + +and + +g +2 + +) and not set on tubercles. The males of 12 species are unknown and the remaining described males have smooth anogential setae ( + +g +1 + +and + +g +2 + +). Therefore, + +E. eorhis + +is suggested as species inquirenda. + + + + \ No newline at end of file diff --git a/data/38/32/87/383287CC0350FFA68E91FA4955C5FBCC.xml b/data/38/32/87/383287CC0350FFA68E91FA4955C5FBCC.xml new file mode 100644 index 00000000000..b9219cb2ad8 --- /dev/null +++ b/data/38/32/87/383287CC0350FFA68E91FA4955C5FBCC.xml @@ -0,0 +1,270 @@ + + + +Two new species of Eupalopsellidae (Acari: Prostigmata: Raphignathoidea) and key to the world species of Exothorhis Summers + + + +Author + +Khan, Eid Muhammad + + + +Author + +Kamran, Muhammad + + + +Author + +Rehman, Muneeb Ur + + + +Author + +Mirza, Jawwad Hassan + + + +Author + +Alatawi, Fahad Jaber + +text + + +Journal of Natural History + + +2024 + +2024-05-16 + + +58 + + +13 - 16 + + +511 +526 + + + +journal article +10.1080/00222933.2024.2331825 +1464-5262 +11239904 + + + + + + +Key to species of + +Exothorhis +Summers + + + + + + + + +1. Palp tarsus with solenidion .............................................................................................................. 2 + + + +- Palp tarsus without solenidion ............................................ + +E. sudanicus +Zaher and Yousaf + + + + + + +2. Palp tibial claw present ..................................................................................................................... 3 + + + + +- Palp tibial claw absent .................................................................................. + +E. armata +Summers + +3. Dorsum of idiosoma covered by two/three shields .............................................................. 4 + + + +- Dorsum of idiosoma covered by more than three shields ................................................. 7 + + + +4. Dorsal body setae mostly spatulate ............................................................................................. 5 + + +- Dorsal body setae mostly tapering .............................................................................................. 6 + + + + + +5. Genu and femur I–IV 1–1–1–1 and 5(1) – 4(1) – 4(1) – 4(1), respectively ........................... .......................................................................................... + +E. damortis +Rimando and Corpuz-Raros + + + + + +- Genu and femur I–IV (2(1)–1(1)–1(1)–1(1)) and (5(2)–5(2)–5(1)–5(1)), respectively ......... .................................................................................................................................. + +E. okinawana +Ehara + + + + + + + +6. Idiosoma covered by two shields ........................................................ + +E. echinocactii +Gerson + + + + + +- Idiosoma covered by three shields ........................ + +E. camelliae +Meyer and Ueckermann + + + + + + +7. Dorsal setae mostly spatulate ......................................................................................................... 8 + + +- Dorsal setae mostly tapering ........................................................................................................ 11 + + + + +8. Postocular body present ................................................................................................................... 9 + + + +- Postocular body absent ........................ ........................ + +E. lenis +Rimando and Corpuz-Raros + + + + + + +9. Tarsus III with solenidion ................................................................................................................ 10 + + + +- Tarsus III without solenidion ................................. + +E. mirus +(Chaudhri, Akbar and Rasool) + + + + + + + +10. Dorsal shield smooth, coxa III without setae ..................... ...................... + +E. kenyae +Bolland + + + + + +- Dorsal shield punctate, coxa III with one seta + +E. saudiensis + + +sp +. +n +. + +Alatawi and Kamran + + + + + +11. Tibia I with small spine like solenidion distally ..................................................................... 12 + + + +- Tibia I without small spine like solenidion distally. + +E. phoenix + +i Meyer and Ueckermann + + + + + +12. Tibia I with 5(1) setae ....................................................................................................................... 13 + + + +- Tibia I with 4(1) setae .................................................................... + +E. jinganensis +Hu and Chen + + + + + + + +13. Tarsi I–II with 9(1)–8(1) setae .................................................................... + +E. caudate +Summers + + + + + +- Tarsi I–II with 8(1)–7(1) setae ................ ................. + +E. matulis +Rimando and Corpuz-Raros + + + + + + + \ No newline at end of file diff --git a/data/38/32/87/383287CC0351FFA58E91FA365516FF79.xml b/data/38/32/87/383287CC0351FFA58E91FA365516FF79.xml new file mode 100644 index 00000000000..1dd9d899f41 --- /dev/null +++ b/data/38/32/87/383287CC0351FFA58E91FA365516FF79.xml @@ -0,0 +1,115 @@ + + + +Two new species of Eupalopsellidae (Acari: Prostigmata: Raphignathoidea) and key to the world species of Exothorhis Summers + + + +Author + +Khan, Eid Muhammad + + + +Author + +Kamran, Muhammad + + + +Author + +Rehman, Muneeb Ur + + + +Author + +Mirza, Jawwad Hassan + + + +Author + +Alatawi, Fahad Jaber + +text + + +Journal of Natural History + + +2024 + +2024-05-16 + + +58 + + +13 - 16 + + +511 +526 + + + +journal article +10.1080/00222933.2024.2331825 +1464-5262 +11239904 + + + + + + + +Exothorhis bixae +Rimando and Corpuz-Raros + +species inquirenda + + + + + + + +Exothorhis bixae +Rimando and Corpuz-Raros, 1996: 112 + + + + + +Remarks + + + +Exothorhis bixae + +was originally described based on +two male +specimens and was distinguished by having leg I longer than other legs and anogential setae ( + +g +1 + +and + +g +2 + +) set on tubercles. Based on 17 published species descriptions and illustrations and observations of more than +100 specimens +(personal observation), the length of leg I males is always longer than other legs and anogential setae in male are set on tubercles. These characters cannot be used to distinguish species. Therefore, + +E. bixae + +is considered a species inquirenda. + + + + \ No newline at end of file diff --git a/data/38/32/87/383287CC035AFFA48FDAFAA55343FA8C.xml b/data/38/32/87/383287CC035AFFA48FDAFAA55343FA8C.xml new file mode 100644 index 00000000000..79e3d225f7d --- /dev/null +++ b/data/38/32/87/383287CC035AFFA48FDAFAA55343FA8C.xml @@ -0,0 +1,761 @@ + + + +Two new species of Eupalopsellidae (Acari: Prostigmata: Raphignathoidea) and key to the world species of Exothorhis Summers + + + +Author + +Khan, Eid Muhammad + + + +Author + +Kamran, Muhammad + + + +Author + +Rehman, Muneeb Ur + + + +Author + +Mirza, Jawwad Hassan + + + +Author + +Alatawi, Fahad Jaber + +text + + +Journal of Natural History + + +2024 + +2024-05-16 + + +58 + + +13 - 16 + + +511 +526 + + + +journal article +10.1080/00222933.2024.2331825 +1464-5262 +11239904 + + + + + + +Exothorhis saudiensis + + +sp. n. + + + + + + +( +Figures 9–16 +) + + + + +Diagnosis (based on female) + + +Dorsum of idiosoma coarsely punctate, without visible striae except for anterior to setae +vi +and +sce +; all dorsal body setae densely denticulate, tips truly spatulate, present on prominent tubercles; relatively long, reaching to the bases of setae next in line; coxal area with fine punctations and coxae III with one seta. + + + + + +Description +(n = 10). + +Measurement of +holotype +followed by +nine paratypes +as ranges (in parentheses). + + + +Figure 9. + +Exothorhis saudiensis + + +sp. n. + +Female, dorsum. + + + + +Dorsum +. ( +Figure 9 +) + +Length of body (excluding gnathosoma) ( + +v +1 +–h +2 + +) 365 (354–374), width 235 (228–248). Dorsum of idiosoma covered by five indistinct shields and coarsely punctate, without visible striae except for anterior to setae +vi +and +sce +; all dorsal body setae strongly denticulate, truly spatulate, on prominent tubercles; relative long, reaching to the base of setae next in line; a pair of eyes present anterolaterally near the base of setae +sci +; postocular bodies located between setae +sci +and +sce +; Length of setae: +vi +58 (55–61), +ve +70 (67–73), +sci +67 (64–72), +sce +70 (67–74), + +c +1 + +73 (70–78), + +c +2 + +68 (65–73), + +d +1 + +64 (60–69), + +d +2 + +68 (63–73), + +e +1 + +68 (65–73), + +e +2 + +84 (79–88), + +f +1 + +78 (75–83), + +h +1 + +45 (41–49), + +h +2 + +32 (30–35). Distance between setae: +vi–vi +15 (30–34), +ve–ve +85 (81–89), +vi–ve +43 (40–48), +ve–sci +47 (43–50), +sci– sce +68 (63–72), +sci–sci +15 (13–17), +sce–sce +146 (140–160), + +c +1 +–c +1 + +15 (11–17), + +c +1 +–c +2 + +70 (68– 73), + +c +2 +–c +2 + +144 (137–150), + +c +1 +–d +1 + +62 (60–67), + +d +1 +–d +1 + +25 (22–28), + +d +2 +–d +2 + +137 (131–150), + +d +1 +–d +2 + +75 (72–78), + +d +1 +– + +e +1 + + +58 (55–60), + +d +2 +–e +2 + +73 (69–78), + +e +1 +– + +e +1 + + +18 (16–20), + +e +1 +– + +e +2 + + +45 (41–48), + +e +2 +–e +2 + +105 (99–107), + +e +1 +–f +1 + +63 (60–68), + +f +1 +–f +1 + +67 (63–70), + +f +1 +–h +1 + +63 (59–68), + +f +1 +–h +2 + +48 (43–52), + +h +1 +–h +1 + +37 (35–40), + +h +1 +–h +2 + +22 (18–25), + +h +2 +–h +2 + +72 (70–74). + + + +Figure 10. + +Exothorhis saudiensis + + +sp. n. + +Female, venter. + + + + +Figures 11, 12. + +Exothorhis saudiensis + + +sp. n. + +Female, +11 – +Sub-capitulum; +12 – +Palp. + + + + +Figures 13–16. + +Exothorhis saudiensis + + +sp. n. + +Female, +13 – +Leg I; +14 + +Leg II; +15 + +Leg III; +16 – +Leg IV. + + + + +Venter +. ( +Figure 10 +) + +First two pairs of anteromedial ventral setae (l +a +and 3 +a +) are very long and whip like; the posterior pair (4 +a +) is almost half the length of the former two setae; venter entirely striated; the anogenital area bears seven pairs of setae; three pairs of aggenital and four pairs of anogenital setae; all setae are relatively long except the fourth pair of anogenital setae, relatively short. Length of setae: l +a +78 (73–80), 1 +b +35 (30–40), 1 +c +32 (29–35), 2 +b +42 (39–45), 3 +a +65 (61–70), 3 +b +34 (31–36), 4 +a +34 (30–40), 4 +b +29 (26–32). Three pairs of aggenital setae ( + +ag +1 +–ag +3 + +), + +ag +1 + +37 (35–39), + +ag +2 + +32 (30–35), + +ag +3 + +30 (28–34). Anogenital area with coarse areolae sculpturing and three setae ( + +ps +1–3 + +) and one pair of genital setae (g + +1 + +), setae + +g +1 + +44 (41–48), + +ps +3 + +25 (23–28), + +ps +2 + +22 (20–25), + +ps +1 + +20 (18–23). Distances between genital setae: + +ag +1 +–ag +1 + +39 (36–43), + +ag +2 +–ag +2 + +35 (33–38), + +ag +3 +–ag +3 + +45 (42– 48), + +g +1 +–g +1 + +24 (22–26), + +ps +3 +–ps +3 + +25 (22–28), + +ps +2 +–ps +2 + +30 (27–32), + +ps +1 +–ps +1 + +18 (16–20). Distances between ventral setae: 1 +a +–1 +a +30 (28–32), 3 +a +–3 +a +42 (40–45), 4 +a +–4 +a +66 (62–69), 1 +b +–1 +c +15 (12–17), 1 +a +–3 +a +89 (85–95), 3 +a +–4 +a +48 (45–52), 4 +a–ag +42 (38–45), + +ag +1 +–g +1 + +38 (35–41), + +g +1 +–ps +3 + +19 (16–22), + +ps +3 +–ps +2 + +15 (12–17), + +ps +2 +–ps +1 + +10 (9–12). + + + +Gnathosoma +. ( +Figures 11–12 +) + +Chelicerae slender, nearly one and a half times as long as movable digits (103:62); Palp tapered, palpgenu about thrice as long as palptibia (31:10), palptibial claw small but distinct, dorsal seta +l +’ +T +(3) about one-ninth length of +l +(16); terminal palptarsal slender, counts of setae and solenidion from palptrochanter to palptarsi: 0, 3, 1, 3, 3 + 1 +ω ++ 2 subterminal eupathidia + 1 terminal eupathidium; subcapitular setae +m +52 (47–58), +n +48 (45–51), +m–m +(18–21), +n–n +15 (13–17) and +m–n +20 (19–23). + +or +1 + +17 (15–20), + +or +2 + +22 (20–25), + +or +1 +– or +2 + +5 (4–7), + +or +1 +– or +1 + +4 (3–5) and + +or +2 +– or +2 + +10 (8–12). + + + +Legs +. ( +Figures 13–16 +) + +Length of leg I 274 (256–279); leg II 250 (240–263); leg III 213 (204–224); leg IV 200 (192–214). Tarsal claws uncinated. Setal formulae of leg segments as follows: coxae 2–1–1–1; trochanters 1–1–1–1; femora 4–4–3–1; genua 1 + 1 +Κ +–1–1–1; tibiae 4 + 1 +φ +ρ–4 + 1 +φ +ρ–4 + 1 +φ +ρ–4 + 1 +φ +ρ; tarsi 10 + 1 +ω +–9 + 1 +ω +–6 + 1 +ω +–6. Tarsus I and II with solenidion, Iω 17 (15–19), IIω 16 (14–17), slender and tapering rather than rod like. + + + + +Etymology. +The specific epithet is derived from the name of the country, +Saudi Arabia +, where the +type +specimens were collected. + + + + +Type materials. +Holotype +female, +three paratype females +, + +Ziziphus mucronata +Willd + +( +Rhamnaceae +), Taif, +Saudi Arabia +, +21.083562°N +, +40.316697°E +, +11 October 2016 +, coll. Muneeb Ur Rehman and M. Kamran; +four paratype females +, + +Punica granatum + +( +Lythraceae +), Taif, +Saudi Arabia +, +21.500145°N +, +40.466723°E +, +10 September 2017 +, coll. Eid M. Khan and Muneeb Ur Rehman; +two paratype females +, + +Tamarix aphylla + +(L.) Karst. ( +Tamaricaceae +), Taif, +Saudi Arabia +, +21.233458°N +, +40.466766°E +, +10 September 2017 +, coll. Eid M. Khan and Muneeb Ur Rehman. + + + + +Remarks. + +Exothorhis saudiensis + + +sp. n. + +is morphologically close to + +E. kenyae +Bolland + +in having dorsal body setae mostly spatulate, and idiosoma covered by five thin shields. However, the new species differs from later species by punctate dorsal shield (vs smooth dorsal shield), coxa III with one seta (vs without setae) and coxal area with punctations (vs coxal area smooth in + +E. kenyae + +). + + + + \ No newline at end of file diff --git a/data/38/32/87/383287CC035BFFAF8FDBF9C75289FB57.xml b/data/38/32/87/383287CC035BFFAF8FDBF9C75289FB57.xml new file mode 100644 index 00000000000..df4ee7083e6 --- /dev/null +++ b/data/38/32/87/383287CC035BFFAF8FDBF9C75289FB57.xml @@ -0,0 +1,95 @@ + + + +Two new species of Eupalopsellidae (Acari: Prostigmata: Raphignathoidea) and key to the world species of Exothorhis Summers + + + +Author + +Khan, Eid Muhammad + + + +Author + +Kamran, Muhammad + + + +Author + +Rehman, Muneeb Ur + + + +Author + +Mirza, Jawwad Hassan + + + +Author + +Alatawi, Fahad Jaber + +text + + +Journal of Natural History + + +2024 + +2024-05-16 + + +58 + + +13 - 16 + + +511 +526 + + + +journal article +10.1080/00222933.2024.2331825 +1464-5262 +11239904 + + + + + +Genus + +Exothorhis +Summers + + + + + + + +Type +species. + + +Exothorhis caudata +Summers, 1960: 131 + +. +Diagnosis. +Based on +Meyer and Ueckermann (1989) +and +Gerson (1994) +. + + + + \ No newline at end of file diff --git a/data/38/32/87/383287CC035CFFA98F8FFA50527FF906.xml b/data/38/32/87/383287CC035CFFA98F8FFA50527FF906.xml new file mode 100644 index 00000000000..84d50f4dd58 --- /dev/null +++ b/data/38/32/87/383287CC035CFFA98F8FFA50527FF906.xml @@ -0,0 +1,103 @@ + + + +Two new species of Eupalopsellidae (Acari: Prostigmata: Raphignathoidea) and key to the world species of Exothorhis Summers + + + +Author + +Khan, Eid Muhammad + + + +Author + +Kamran, Muhammad + + + +Author + +Rehman, Muneeb Ur + + + +Author + +Mirza, Jawwad Hassan + + + +Author + +Alatawi, Fahad Jaber + +text + + +Journal of Natural History + + +2024 + +2024-05-16 + + +58 + + +13 - 16 + + +511 +526 + + + +journal article +10.1080/00222933.2024.2331825 +1464-5262 +11239904 + + + + + +Genus + +Eupalopsellus +Sellnick, 1949 + + + + + + + +Type +species. + + +Eupalopsellus olandicus +Sellnick, 1949: 132 + +. + + + + +Diagnosis. +Based on +Fan (2004) +and + +Khanjani +et al +. (2011) + +. + + + + \ No newline at end of file diff --git a/data/38/32/87/383287CC035FFFAE8FDCFF2355C2F9F0.xml b/data/38/32/87/383287CC035FFFAE8FDCFF2355C2F9F0.xml new file mode 100644 index 00000000000..7633ce7d3f3 --- /dev/null +++ b/data/38/32/87/383287CC035FFFAE8FDCFF2355C2F9F0.xml @@ -0,0 +1,845 @@ + + + +Two new species of Eupalopsellidae (Acari: Prostigmata: Raphignathoidea) and key to the world species of Exothorhis Summers + + + +Author + +Khan, Eid Muhammad + + + +Author + +Kamran, Muhammad + + + +Author + +Rehman, Muneeb Ur + + + +Author + +Mirza, Jawwad Hassan + + + +Author + +Alatawi, Fahad Jaber + +text + + +Journal of Natural History + + +2024 + +2024-05-16 + + +58 + + +13 - 16 + + +511 +526 + + + +journal article +10.1080/00222933.2024.2331825 +1464-5262 +11239904 + + + + + + +Eupalopsellus taifensis + + +sp. n. + + + + + + +( +Figures 1–8 +) + + + + +Diagnosis (based on female) + + +Dorsal shields punctate; all dorsal body setae on small tubercles; seta + +c +2 + +on platelets, postocular bodies ( +pob +) nearly twice as large as eyes; humeral platelets obvious; setae + +e +1 + +and + +f +1 + +shorter than distances to setae next in line, trochanter IV with a seta, femur III with three setae and tarsus IV with a solenidion +ω +. + + + + + +Description +(n = 16). + +Measurement of +holotype +followed by +15 paratypes +as ranges (in parentheses). + + + +Dorsum +. ( +Figure 1 +) + +Length of body (excluding gnathosoma) ( + +v +1 +–h +2 + +) 315 (304–324), width 219 (208–228). Body oval; dorsum is covered by four distinct shields, the propodosomal, metapodosomal, opisthosomal and suranal shields; dorsal integument striated except the shields; all the dorsal shields finely punctate; setae situated on small tubercles; propodosomal shield truncate posteriorly bearing four pairs of setae ( +vi +, +ve, sci +and +sce +), a pair of eyes 9 (8–10), and a pair of post-ocular bodies ( +pob +) 20 (18–21) in diameter, anterior margin of dorsal propodosomal shield with inverted V-shaped striae, the space between propodosomal and opisthosomal shield (CD) with transverse striae; the striae lateral to CD and EF shields striated longitudinally; CD, EF and H shields with three, three and two pairs of setae, respectively; humeral setae situated on small shields; all the dorsal body setae slender, pointed and pectinate; + +f +1 + +longest dorsal body setae. Length of setae: +vi +15 (13–16), +ve +20 (18–22), +sc1 +21 (20–22), +sce +23 (21–24), + +c +1 + +15 (13–17), + +c +2 + +30 (28–33), + +d +1 + +23 (20–25), + +d +2 + +21 (20–24), + + +e +1 + +25 + +(23–28), + + +e +2 + +23 + +(21–25), + +f +1 + +39 (37–43), + +h +1 + +35 (33–39), + +h +2 + +33 (30–38). Distance between setae: +vi–vi +31 (30–34), +ve–ve +58 (54–60), +vi–ve +23 (20–25), +ve– sci +32 (30–36), +sci–sce +40 (36–44), +sci–sci +10 (9–12), +sce–sce +95 (92–99), + +c +1 +–c +1 + +74 (71–77), + +c +1 +– c +2 + +50 (47–53), + +c +2 +–c +2 + +144 (137–150), + +c +1 +–d +1 + +55 (53–58), + +d +1 +–d +1 + +33 (31–38), + +d +2 +–d +2 + +117 (111–122), + +d +1 +– + +e +1 + + +58 (55–60), + +d +2 +– + +e +2 + + +42 (39–45), + +e +1 +–e +1 + +72 (68–75), + +e +1 +– + +e +2 + + +25 (23–28), + +e +2 +–e +2 + +102 (97–109), + +e +1 +–f +1 + +29 (27–30), + +f +1 +–f +1 + +67 (63–70), + +f +1 +–h +1 + +53 (49–56), + +f +1 +–h +2 + +43 (39–47), + +h +1 +–h +1 + +37 (35–40), + +h +1 +–h +2 + +20 (18–23), + +h +2 +–h +2 + +72 (70–74). + + + +Venter +. ( +Figure 2 +) + +The anterior (1 +a +) and median (3 +a +) pairs of setae are very long and whip-like; the posterior pair (4 +a +) is almost half the length of the former two setae (4 +a +); venter entirely striated; the anogenital area bears seven pairs of setae; three pairs of aggenital setae ( + +ag +1–3 + +) and four pairs of anogenital setae (g + +1 + +, + +ps +1–3 + +), all setae are relatively long except the fourth pair of anogenital setae ( + +ps +1 + +), which is relatively short. A tooth-like structure is located on each side of anogenital shield in a latero-posterior position. Length of setae: l +a +92 (88–198), 1 +b +27 (21–30), 1 +c +22 (19–25), 2 +b +32 (29–35), 3 +a +75 (71–80), 3 +b +24 (21–26), 3 +c +25 (22–28), 4 +a +51 (48–54), 4 +b +19 (16–22), 4 +c +21 (20–24). Three pairs of aggenital setae ( + +ag +1 +– +3 + +), + +ag +1 + +37 (35–39), + +ag +2 + +32 (30–35), + +ag +3 + +30 (28–34). Anal shield with coarse areolae sculpturing and three pairs of pseudoanal setae ( + +ps +1–3 + +) and one pair of genital setae ( + +g +1 + +), setae + +g +1 + +40 (36–43), + +ps +3 + +28 (26–30), + +ps +2 + +22 (20–25), + +ps +1 + +20 (20–23). Distance between setae: 1 +a +–1 +a +37 (35–40), 3 +a +–3 +a +73 (70–77), 4 +a +–4 +a +52 (50–55), 1 +b +–1 +c +11 (10–13), 1 +a +–3 +a +110 (103–119), 3 +a +–4 +a +83 (80–90), 4 + +a–ag +1 + +68 (63–72), + +ag +1 +–g +1 + +45 (42–49), + +g +1 +–ps +3 + +17 (15–20), + +ps +3 +–ps +2 + +12 (10–15), + +ps +2 +–ps +1 + +7 (6–8), + +ag +1 +–ag +1 + +31 (29–34), + +g +1 +–g +1 + +20 (19–229), + +ps +3 +–ps +3 + +28 (25–30), + +ps +2 +–ps +2 + +30 (27–32), + +ps +1 +–ps +1 + +18 (16–20). + + + +Figure 1. + +Eupalopsellus taifensis + + +sp. n. + +Female, dorsum. + + + + +Figure 2. + +Eupalopsellus taifensis + + +sp. n. + +Female, venter. + + + + +Figures 3, 4. + +Eupalopsellus taifensis + + +sp. n. + +Female, +3 – +Sub-capitulum; +4 – +Palp. + + + + +Gnathosoma +. ( +Figures 3–4 +) + +Chelicerae slender, nearly one and a half times as long as movable digits (114: 68); Palp tapered, palpgenu about thrice as long as palptibia (35:12), palptibial claw minute, dorsal seta +l +’ +T +(2) about one-ninth length of +l +(19); terminal palptarsal eupathidium 7; counts of setae and solenidion from palptrochanter to palptarsi: 0, 3, 1, 3, 3 + 1 ω + 2 subterminal eupathidia + 1 terminal eupathidium; subcapitular setae +m +40 (37–43), +n +38 (35–41), +m–m +(18–21), +n–n +15 (13–17) and +m–n +20 (19–23). + + + +Legs +. ( + +Figures 5 + +8 + +) + +Length of leg I 164 (156–169); leg II 137 (132–143); leg III 133 (127–139); leg IV 140 (136–144). Tarsal claws uncinate. Setal formulae of leg segments as follows: coxae 2–1–2–2; trochanters 1–1–1–1; femora 4–4–3–1; genua 1 + +Κ +–1–1–1; tibiae 5 + 1 +φ +ρ–4 + 1 +φ +ρ–4 + 1 +φ +ρ–4 + 1 +φ +ρ; tarsi 10 + 1 +ω +–9 + 1 +ω +–6 + 1 +ω +–6 + 1 +ω +. Tarsi I and II with solenidia, I +ω +9 (7–10), II +ω +5 (4–7), slender and tapering rather than rod like. + + + + +Etymology. +The specific epithet is derived from the name of the city ‘Taif’ where the +type +specimens were collected. + + + + +Type materials. +Holotype +female, +three paratype females +, + +Juniperus procera +Hochst. ex Endl. + +( +Cupressaceae +), Taif, +Saudi Arabia +, +21.100134°N +, +40.333479°E +, +12 September 2017 +, coll. Eid M. Khan and Muneeb Ur Rehman; +two paratype females +, + +Juniperus procera +Hochst. ex Endl. + +( +Cupressaceae +), Taif, +Saudi Arabia +, +21.416795°N +, +40.416738°E +, +14 September 2017 +, coll. Eid M. Khan and Muneeb Ur Rehman; +six paratype females +, + +Prunus korshinskyi +Hand. + +- Mazz ( +Rosaceae +), Taif, +Saudi Arabia +, +21.333578°N +, +40.316798°E +, +12 October 2016 +, coll. Eid M. Khan and Muneeb Ur Rehman; +two paratype females +, + +Acacia +sp. + +, (Leguminosae), Taif, +Saudi Arabia +, +21.100133°N +, +40.316832°E +, +11 September 2017 +, coll. Eid M. Khan and Muneeb Ur Rehman; +two paratype females +, + +Crataegus sinaica +Boiss + +( +Rosaceae +), Taif, +Saudi Arabia +, +21.350082°N +, +40.316819°E +, +11 September 2017 +, coll. Eid M. Khan and Muneeb Ur Rehman. + + + + +Remarks. + +Eupalopsellus taifensis + + +sp. n. + +is morphologically close to + +E. orebiosis +Meyer and Ueckermann, 1984 + +and + +E. sellnicki +, + +Meyer and Ueckermann, +1984 + + +in: leg tarsus IV each with a solenidion ( +ω +), dorsal body shields punctate and femur III with three setae. However, the new species differs from + +E. orebiosis + +due to trochanter IV with one seta (vs without seta), setae + +c +2 + +on platelets (vs setae + +c +2 + +on integument), coxal area with punctations (vs coxal area smooth), and setae + +e +1 + +and + +f +1 + +shorter than distance to setae next in line (vs setae + +e +1 + +and + +f +1 + +crossing setae next in line). Moreover, the new species differs from + +E. sellnicki + +in the combination of characters: postocular bodies twice as large as eyes (vs postocular bodies 4–5 times larger than eyes); coxal area with punctations (vs coxal area smooth), setae + +e +1 + +and + +f +1 + +shorter than distance to setae in line (vs setae + +e +1 + +and + +f +1 + +crossing setae next inline). + + + + \ No newline at end of file diff --git a/data/38/32/A4/3832A42C784656678C50E9CD54FFF148.xml b/data/38/32/A4/3832A42C784656678C50E9CD54FFF148.xml new file mode 100644 index 00000000000..acde188e4a5 --- /dev/null +++ b/data/38/32/A4/3832A42C784656678C50E9CD54FFF148.xml @@ -0,0 +1,112 @@ + + + +A revision of European species of the genus Tetrastichus Haliday (Hymenoptera: Eulophidae) using integrative taxonomy + + + +Author + +Hansson, Christer +The Natural History Museum, London, United Kingdom & Biological Museum (Entomology), Lund University, Lund, Sweden +christerdennis@gmail.com + + + +Author + +Schmidt, Stefan +https://orcid.org/0000-0001-5751-8706 +SNSB-Zoologische Staatssammlung Muenchen, Munich, Germany +schmidt.s@snsb.de + +text + + +Biodiversity Data Journal + + +2020 + +2020-12-16 + + +8 + + +59177 +59177 + + + + +http://dx.doi.org/10.3897/BDJ.8.e59177 + +journal article +http://dx.doi.org/10.3897/BDJ.8.e59177 +1314-2828-8-e59177 +AD70B3AB67634D2885F290988225C5C8 +2BC7CCC36D765F1C87ACBE8025DFD848 + + + + +Tetrastichus perkinsorum Graham, 1991 + + + + +Tetrastichus perkinsorum +Graham 1991 +:234. Holotype ♀ in NHM, examined (Fig. +85 +). + + + +Description + +See +Graham (1991) +. + + + +Diagnosis + +Mouth opening 1.4 +x +malar space; antenna with scape 1.2 +x +as long as an eye, funiculars 1.5-1.6 +x +as long as wide. + + + +Distribution + +Sweden ( +Graham 1991 +). + + + +Ecology + + +Host +Unknown. + + +Material examined + +Holotype ♀ of + +T. perkinsorum + +(NHM, type no. 5.3624). + + + + \ No newline at end of file diff --git a/data/38/33/B0/3833B055B0AA439FE9154B36F9CCD456.xml b/data/38/33/B0/3833B055B0AA439FE9154B36F9CCD456.xml new file mode 100644 index 00000000000..daa035fbe8b --- /dev/null +++ b/data/38/33/B0/3833B055B0AA439FE9154B36F9CCD456.xml @@ -0,0 +1,150 @@ + + + +Nesting behavior and ecological preferences of five Diphaglossinae species (Hymenoptera, Apoidea, Colletidae) from Argentina and Chile + + + +Author + +Sarzetti, Laura C. +CONICET, Division Icnologia, Museo Argentino de Ciencias Naturales " Bernardino Rivadavia ", Av. Angel Gallardo 470, 1405. Buenos Aires, Argentina +lsarzetti@macn.gov.ar + + + +Author + +Genise, Jorge F. +CONICET, Division Icnologia, Museo Argentino de Ciencias Naturales " Bernardino Rivadavia ", Av. Angel Gallardo 470, 1405. Buenos Aires, Argentina + + + +Author + +Sanchez, M. Victoria +CONICET, Division Icnologia, Museo Argentino de Ciencias Naturales " Bernardino Rivadavia ", Av. Angel Gallardo 470, 1405. Buenos Aires, Argentina + + + +Author + +Farina, Juan L. +Museo Municipal de Ciencias Naturales " Lorenzo Scaglia ", Area Entomologia, Av. Libertad 3099, Plaza Espana, 7600 Mar del Plata, Buenos Aires, Argentina + + + +Author + +Molina, M. Alejandra +CONICET, Instituto Superior de Entomologia, Facultad de Ciencias Naturales, Miguel Lillo 205, 4000 S. M. de Tucuman, Argentina + +text + + +Journal of Hymenoptera Research + + +2013 + +2013-08-01 + + +33 + + +63 +82 + + + + +http://dx.doi.org/10.3897/jhr.33.5061 + +journal article +http://dx.doi.org/10.3897/jhr.33.5061 +1314-2607-33-63 +7D155703F503537C5C5AFFCDF60FFFE6 +574823 + + + + + +Diphaglossa gayi Spinola, 1851 + + + +Localities and nesting sites. + +The observations were carried out during November 8th, 2009 and February 10th, 2011 beside the +Rio +Negro Bridge ( +42°57.433'S +, +72°39.233'W +) and during November 9th, 2009 and February, 15th, 2011 at Lonconao +( +43°13.007'S +, +71°55.143'W +), both localities from the Palena province (Region de Los Lagos, Chile). The nesting sites occur in the glades of hygrophilous evergreen forests with a MAT around 11° C and MAP around 2500-3000 mm. Two nests were excavated. The first nest was located in a steep slope in a farm beside the +Rio +Negro Bridge ( +Fig. 38 +), where +as +the second was excavated in a low vertical section of the soil in another farm at Lonconao ( +Fig. 39 +). At both localities, the soil, composed of silty to very fine sandy material and devoid of rocks, contained grass rhizomes, some roots, and earthworm burrows. The soil cover consisted of a combination of dense grasses and dicots ( +Fig. 38 +), and the subsurface contained a thin ash layer produced by the Chaiten eruption of May 2008. + + + +Figures 38-43. + +Diphaglossa gayi + +Spinola, 1851. +38 +General view of the nesting site beside the +Rio +Negro Bridge, Chile +39 +general view of nesting site at Lonconao, Chile +40 +tumulus of soil pellets and open entrance +41 +main tunnel +42 +nest architecture +43 +cell, neck with lining, and egg laying on provisions. + + + + + +Daily +activity. + +On November 8th, 2009 the first nest was found around 06:00 pm and the female was observed entering the nest with pollen around 07:00 pm. On November 9th, 2009 the second nest was found also around 06:00 pm and the female was inside the main tunnel. + + +Description of nests. + +The Rio Negro nest showed an open circular entrance, 0.5 cm in diameter, which was surrounded by an eccentric tumulus, roughly 4.6 cm wide and 5.2 cm long. The tumulus was composed of soil pellets, probably of the recently deposited subsurface ash layer, which were paler than the soil surface ( +Fig. 40 +). The Lonconao nest was located in a vertical cut, thus the entrance, 0.7 in diameter, lacked a tumulus. Both nests share the same general structure. The main tunnel, circular in cross section, 32-38 cm long, was nearly straight and slightly inclined downwards, ending in a vertical segment 8 cm long ( +Figs 41 and 42 +). Its maximum diameter was 0.7-1.0 cm. Each nest contained four closed cells arranged in two pairs, one pair near the middle portion of the main tunnel, and the other near the end. It is possible that both cells were connected to the main tunnel by a common lateral, filled with soil when the nest was excavated ( +Fig. 42 +). The cellswere vertical, rounded at the bottom, and the neck was strongly curved ( +Figs 42 and 43 +). The vertical portion of the cells was 2 cm long and 1 cm in maximum diameter (n: 8). The neck was 0.7 cm in diameter. The inner surface of cells and the neck was lined with a whitish semitransparent, cellophane-like material. The cells in both nests contained one egg laying on top of the semiliquid provisions. The cell closure was not observed. + + + + + \ No newline at end of file diff --git a/data/38/34/62/383462F506C15E4FA16B4B78EE50C5C8.xml b/data/38/34/62/383462F506C15E4FA16B4B78EE50C5C8.xml new file mode 100644 index 00000000000..b0efada22d4 --- /dev/null +++ b/data/38/34/62/383462F506C15E4FA16B4B78EE50C5C8.xml @@ -0,0 +1,168 @@ + + + +Taxonomic study of Baeosega and its allies, with description of a new species of Nipponosega (Hymenoptera, Chrysididae, Amiseginae) + + + +Author + +Mita, Toshiharu +https://orcid.org/0000-0001-8322-6045 +Entomological Laboratory, Faculty of Agriculture, Kyushu University, Motooka 744, Nishi-ku, Fukuoka 819 - 0395, Japan +t3mita@agr.kyushu-u.ac.jp + +text + + +ZooKeys + + +2021 + +2021-05-31 + + +1041 + + +1 +25 + + + + +http://dx.doi.org/10.3897/zookeys.1041.66267 + +journal article +http://dx.doi.org/10.3897/zookeys.1041.66267 +1313-2970-1041-1 +D7AA23EA975C4195927EE76C377FCF48 +9086C8941CCE58D5AFED14226CEA4232 + + + + +Nipponosega lineata +sp. nov. +Figures 1D +, 7 + + + +Specimen examined. + + +Holotype +. + +Thailand ♀ (THNHM-I-23985), "[NW Thailand] / Tak prov., / Umphang WS, / nr Pha Lueat stn.", "28. i 2015 / Sk. Yamane leg. / 390 m alt.; leaf /& surface soil", "Sk Yamane Collection" (THNHM). + + + +Diagnosis. + + +Nipponosega lineata + +sp. nov. is readily distinguished from other + +Nipponosega + +species by the longitudinally costate pronotum (Fig. +7D +). Other characters useful to distinguish from other species are as follows: body length 2.8 mm; head black, punctate with interspaces smooth, posterior margin of vertex longitudinally costate (Fig. +7D +); maximum interocular distance 2.9 +x +longer than width of frons; lateral ocelli almost touching the inner margin of eye; malar sulcus indicated as a faint track (Fig. +7C +); outer orbit of eye with a row of punctures; occipital carina present (Fig. +7B, D +), reaching lower gena; antenna blackish with scape and F1 testaceous; mesosoma reddish but dorsum largely black; mesoscutum and mesoscutellum punctate; legs brownish; metasoma dark brown, smooth. Male is unknown. + + + +Figure 7. + +Nipponosega lineata + +sp. nov., holotype ♀ +A +head in frontal view +B +ditto, dorsal view +C +ditto, lateral view +D +vertex and mesosoma. Scale bars: 0.5 mm. + + + + +Description. + + +Holotype +female. + +Body length 2.81 mm. Head (Fig. +7A-C +) punctate except scapal basin and posterior margin of vertex, as long as wide in dorsal view, 0.82 +x +as wide as deep in frontal view; punctures 0.5-1.0 +x +MOD, 0.5-2.0, 2.0-3.0, and, 0.5-1.0 punctures diameter apart on frons, ocellar region and vertex, respectively; interspaces among punctures smooth; scapal basin moderately excavated, transversely costate by fine grooves, upper part with short median unsculptured line; malar sulcus indicated as faint track; frons narrow, shortest distance between eyes 0.23 +x +head width; maximum interocular distance 2.9 +x +as long as narrowest width of frons; MS 0.23 +x +as long as eye height; outer orbit of eye with a row of deep punctures; ocellar triangle acute, lateral ocelli almost touching inner margin of eye; OL 1.3, OPL 2.2, POL 1.0, OOL 0.2, MOD 0.3; posterior margin of vertex longitudinally costate; occipital carina present, reaching gena. Clypeus thickened. Mandible without inner tooth, cylindrical. Antenna stout, F4-F9 wider than long; length (width) of F1 to F4 following ratio: 5.8 (1.5): 1.8 (1.7): 1.8 (1.8): 1.5 (2.0). + + +Pronotum (Fig. +7D +) longitudinally costate by fine grooves except anterior narrow region smooth with several punctures; medial longitudinal line reaching 3/4 of pronotum; length of pronotum measured mesad 0.89 +x +as long as wide, 1.6 +x +mesoscutum plus mesoscutellum. Mesoscutum roughly punctate-reticulate: punctures as long as or slightly smaller than MOD; notauli complete, diverging anteriorly. Mesoscutellum punctate as mesoscutum, 0.59 +x +longer than mesoscutum. Mesopleuron punctate with smooth interspaces: punctures as long as MOD. Metanotum triangular, as long as mesoscutellum mesad, punctate. Propodeum (Fig. +7D +) with postero-lateral corner rounded; dorsal surface long, smooth, transversely rugose; posterior surface transversely rugose; lateral surface obliquely rugose; metapleural region smooth but behind meso-metapleural suture costate. Middle and hind coxae transversely costate. + + +Metasoma smooth, covered with sparse setae; setae 2.5 +x +MOD. + + + +Color +. + +Head black. Antenna basally testaceous with distal apex of scape and pedicel dark brown, F2-F10 black. Mandible brown. Mesosoma reddish but following parts blackish: dorsal surface of pronotum, anterior 2/3 of propleuron, mesoscutum, mesoscutellum, ventral surface of mesepisternum, median enclosure of metanotum, postero-dorsal surface of propodeum. Tegula and wings brown. Coxae whitish with postero-dorsal dark spot; trochanters testaceous; fore femur brown with basal and distal parts testaceous; middle and hind femora brown with basal parts testaceous; tibiae brown with basal parts of fore and hind tibiae testaceous; tarsi testaceous with fore and hind tarsi basally brownish. Metasoma dark brown with anterior surface of T1 and S1 paler. + + + +Distribution. +Thailand (Tak Province). + + +Etymology. + +The specific name derives from the Latin word + +Nipponosega lineata + +, referring to the presence of striae on the pronotum. + + + +Remarks. +The holotype was collected from the leaf litter. + + + \ No newline at end of file diff --git a/data/38/34/DB/3834DB60F6FB52A094705D2570931767.xml b/data/38/34/DB/3834DB60F6FB52A094705D2570931767.xml new file mode 100644 index 00000000000..67f93ec6ef4 --- /dev/null +++ b/data/38/34/DB/3834DB60F6FB52A094705D2570931767.xml @@ -0,0 +1,243 @@ + + + +Tetracha Hope 1838 of the Turks and Caicos Islands (Coleoptera, Carabidae, Cicindelinae) + + + +Author + +Ward 1, Robert D. +Research Associate, Section of Invertebrate Zoology, Carnegie Museum of Natural History; Home address: 41708 North Signal Hill Court, Anthem, AZ 85086 USA + + + +Author + +Davidson, Robert L. +Section of Invertebrate Zoology, Carnegie Museum of Natural History, 4400 Forbes Avenue, Pittsburgh PA 15213 USA +davidsonr@carnegiemnh.org + + + +Author + +Brzoska, David +Research Associate: Carnegie Museum of Natural History; Florida State Collection of Arthropods; University of Kansas Biodiversity Institute, Division of Entomology; Home address: 2740 Island Pond Lane, Naples FL 34119 USA + +text + + +ZooKeys + + +2011 + +2011-11-16 + + +147 + + +85 +97 + + + + +http://dx.doi.org/10.3897/zookeys.147.2104 + +journal article +http://dx.doi.org/10.3897/zookeys.147.2104 +1313-2970-147-85 +F41E17F6A7274DD7855FF3F8FA0C152C +FFD4913B1D2DFFF6BF05E76DF728FFE4 +577428 + + + + + +Tetracha (Tetracha) sobrina caicosensis +subsp. n. +Figs 9 +-11 + + + +Type material. + +(45 specimens) +Holotype ♂: "TURKS & CAICOS/ ISLANDS, South Caicos-/ Victoria Salina, 1m/ +21°29.6'N +, +71°31.5 W +/ D. Brzoska 5-7-I-2010" (CMNH). Allotype ♀: same data as holotype (SEMC). Paratypes (43) as follows: 30 same data as holotype (12 ♂♂, 7 ♀♀ DBC; 2 ♂♂, 2 ♀♀ CMNH; 1 ♂, 1 ♀ AMNH; 1 ♂, 1 ♀ FSCA; 1 ♂, 1 ♀ RNC; 1 ♂ SEMC); 13 labelled: "TURKS & CAICOS/ ISLANDS, Grand Turk-N./ end Saunders Pond, 1m/ +21°29.1'N +, +71°08.9'W +/ D. Brzoska 11-13-I-2010" (11♂♂, 1♀ DBC; 1 ♂ CMNH). + + + +Type locality. +South Caicos Island in the Turks & Caicos Islands group. + + +Distribution. +Known only from two islands in the Turks & Caicos Islands group: South Caicos Island and Grand Turk Island. + + +Etymology. + +A geographic name formed from +"Caicos," +the islands on which this subspecies has been found, and the Latin suffix "- +ensis +," meaning of or from that place. + + + +Diagnosis. + +This new subspecies is similar to the other six subspecific taxa of + +Tetracha sobrina + +, closest to + +Tetracha sobrina infuscata + +(Mannerheim), but differs in the reduced size of its apical lunules (narrow, more or less parallel-sided), green (not blue) elytral margins; small, round, basal trans-sutural coppery-red spot; and broad, black medial band. + + + +Description. + +( +Figs 9-10 +). Length males (n=15) 13.3-15.8 mm; females (n=13) 14.1-16.4 mm. Most similar to + +Tetracha (Tetracha) sobrina infuscata + +(Mannerheim). All appendages pale except antennomeres 2-4 which have small distal brown spots opposite eyes and distal tips of femora which are infuscated. Clypeus and frons metallic green; vertex coppery, duller (South Caicos) to redder (Grand Turk), but never the bright red of + +Tetracha sobrina infuscata + +. Pronotum red with green highlights, especially the posterior transverse +line +, but again not the bright red of + +Tetracha sobrina infuscata + +. Elytra (excluding green punctures) with base with a small trans-sutural, rounded red spot; lateral margins, between the elytral base and the anterior tip of the apical lunule, clearly metallic green; the remainder of the elytra black, no violet areas toward the elytral apices; apical lunule narrow, parallel-sided, inner margin less distinct with scattered disjunct pale cells. Elytral sculpturing consists of punctation over basal half, pits deep blue-green; pits separated by smooth, shiny metallic surface, with very little trace of imbrications or granules; punctures are weakly aligned transversely; posteriorly, pits decrease in size and density while becoming increasingly imbricated, and merge into shingle-like transverse rows, especially between the apical lunules; pits and imbrications greatly reduced to absent on lunules. + + + +Discussion. + +The characters separating this subspecies are somewhat superficial ones of color and texture, but as this is largely all that separates the six described subspecies of this wide-ranging species (see +Naviaux 2007 +), and as these characters seem to be relatively constant over large populations, it seems appropriate enough to describe these isolated island populations from the Turks and Caicos Islands as a new subspecies. The new subspecies is easily separated from five of the six currently recognized subspecies ( +Naviaux 2007 +) by the very black color of the elytra, starting in +front +of the apical lunules and reaching more or less to the base along the suture, and by the relatively narrow and parallel-sided apical lunules. The other five subspecies all have bright metallic colors along the elytral suture, and broader, rounded apical lunules, in most individuals more comma-shaped or globular (these are three mainland subspecies ( + +Tetracha sobrina punctata + +(Laporte), + +Tetracha sobrina freyi + +(Mandl) and + +Tetracha sobrina guyanensis + +Naviaux), one subspecies both mainland and Lesser Antilles ( + +Tetracha sobrina sobrina + +(Dejean)), and one subspecies in the Lesser Antilles ( + +Tetracha sobrina antiguana + +Leng and Mutchler)). The most similar subspecies is + +Tetracha sobrina infuscata + +(Mannerheim) from Cuba, Hispaniola, Puerto Rico and the Virgin Islands. Our new subspecies differs from this mainly in the extent of the blackened center of the elytra, and in the shape of the apical lunules. + +Tetracha sobrina caicosensis + +has the elytra black from the apical lunules to at least the anterior third, and in many individuals more or less all the way to the base, and the green marginal band is very narrow. The apical lunules are narrow and usually parallel to the elytral margin; in some individuals somewhat broader, but still always narrower than in + +Tetracha sobrina infuscata + +, with the incision between the two lunules wider and the medial border much more jagged or irregular. + +Tetracha sobrina infuscata + +has the elytra blackened just in front of the apical lunules, but only in the apical third or so, becoming gradually more metallic green in the anterior two-thirds, and the green marginal band is broader. The apical lunules are very wide, with a relatively narrow incision between the two lunules, and with the medial border very sharply defined and regular. + + + + +Habitat +and collecting notes. + + +At Victoria Salina on South Caicos Island, taken on the edges of dirt roads, mostly at a large open dry sandy area away from the wet salt flats. + +Cicindela boops + +and + +Cicindela trifasciata + +were taken nearby, but in moist saline areas +. +The + +Cicindela + +were taken mostly during the day, with a few at night; the + +Tetracha + +were all taken at night. At Saunders Pond on Grand Turk Island ( +Fig. 11 +), taken at the edge of the pond and at damp saline areas, some with green algal mats. This is a much wetter habitat than Victoria Salina. A single + +Cicindela trifasciata + +was also taken. + + + +Figures 9-10. +Dorsal habitus of + +Tetracha sobrina caicosensis + +; male, length 14.5 mm +9 +female, length 16.0 mm +10 +. + + + + +Figure 11. +Habitat of + +Tetracha sobrina caicosensis + +, Grand Turk + + + + + + \ No newline at end of file diff --git a/data/38/34/FB/3834FB12DCAB5BC99FEDAA5C195E0D09.xml b/data/38/34/FB/3834FB12DCAB5BC99FEDAA5C195E0D09.xml new file mode 100644 index 00000000000..9fae44602ea --- /dev/null +++ b/data/38/34/FB/3834FB12DCAB5BC99FEDAA5C195E0D09.xml @@ -0,0 +1,97 @@ + + + +Phylogenetic relationships of ' Polyalthia ' in Fiji + + + +Author + +Xue, Bine +College of Horticulture and Landscape Architecture, Zhongkai University of Agriculture and Engineering, Guangzhou 510225, Guangdong, China +https://orcid.org/0000-0002-4515-4316 +xuebine@zhku.edu.cn + + + +Author + +Chen, Yanwen +Division of Ecology & Biodiversity, School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China +https://orcid.org/0000-0003-3147-0278 + + + +Author + +Saunders, Richard M. K. +Division of Ecology & Biodiversity, School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China +https://orcid.org/0000-0002-8104-7761 + +text + + +PhytoKeys + + +2020 + +165 + + +99 +113 + + + + +http://dx.doi.org/10.3897/phytokeys.165.57094 + +journal article +http://dx.doi.org/10.3897/phytokeys.165.57094 +1314-2003-165-99 +B613CF89F07A5AF39CA00749906BE07E + + + + +Huberantha vitiensis (Seem.) Chaowasku, Kew Bulletin 70(2)-23: 3. 2015. + + + +Basionym. + + +Polyalthia vitiensis + +Seem., Flora Vitiensis 1: 4, pl. 3. 1865. + + + +Homotypic synonym. + + +Hubera vitiensis + +(Seem.) Chaowasku, Phytotaxa 69: 51. 2012. + + + +Heterotypic synonym. + + +Polyalthia pedicellata + +A.C.Sm., Bulletin of the Bernice P. Bishop Museum 141: 61, fig. 29. 1936. + + + +Type. + +Fiji, Ovalau, near Port Kinnaird, Jul. 1860, +B. Seemann 4 +(holotype: K[K000691678]). + + + + \ No newline at end of file diff --git a/data/38/35/63/38356397535C0C599F1E49755952CAE5.xml b/data/38/35/63/38356397535C0C599F1E49755952CAE5.xml new file mode 100644 index 00000000000..3a4286e8334 --- /dev/null +++ b/data/38/35/63/38356397535C0C599F1E49755952CAE5.xml @@ -0,0 +1,416 @@ + + + +Info Flora Schweiz - Poaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/poaceae.html + +url + + + + + +Bromus madritensis +L. + + + + + +Madrider Trespe + + + + +Art ISFS: 66400 Checklist: 1007420 +Poaceae +Bromus +Bromus madritensis L. + + + +Bestimmungsschluessel + + + +Zusammenfassung + + + + +Artbeschreibung + +(nach +Lauber & al. 2018 +) + +: 10-30(-50) cm hoch, kahl oder zerstreut behaart. +Blaetter +4-8 mm +breit. +Blatthaeutchen +bis +3 mm +lang, fein zerschlitzt. + +Rispe +5-15 cm +lang, dicht, aufrecht, +Aeste +schief aufrecht, meist +5-20 mm +lang + +. Diese ohne die Grannen +2-3 cm +lang. Deckspelze +12-20 mm +lang, + +ihre Granne etwa ebenso lang oder etwas +laenger + +. Untere +Huellspelze +1-, obere 3nervig. + + + + +Bluetezeit + +(nach +Lauber & al. 2018 +) + +: 4-6 + + +Standort und Verbreitung in der Schweiz + +(nach +Lauber & al. 2018 +) + +: +Wegraender +, Bahnareale, +Trockenplaetze +/ kollin / CH vereinzelt adventiv + + + + +Verbreitung global + +(nach +Lauber & al. 2018 +) + +: Mediterran + + + + +Oekologische +Zeigerwerte + +(nach +Landolt & al. 2010 +) + +133+554.t.2n=28 + + + +Anatomie + +Zusammenfassung der Stammanatomie + + +Umriss rund oder oval. +Leitbuendel +in einer Reihe. Kleine Interzellularen, oft dreieckig. Epidermiszellen verholzt. Chlorenchyma in tangential +verlaengerten +Gruppen. + + +Beschreibung (Englisch) + + +Culm-diameter +0.5-1 mm +, wall large, radius of culm in relation to wall thickness 1:0.5. Outline circular wavy. Culm-center hollow and surrounded by a few thin-walled, not lignified cells. Epidermis-cells thick-walled all around. Large vascular bundles arranged in one peripheral row. Chlorenchyma in tangentially enlarged groups. Sclerenchyma in a large, peripheral continuous belt (> 3 cells). Cells medium thick-walled. Small sclerenchymatic sheath with 1-2 cells around vascular bundles. Largest vessels in vascular bundles in lateral position. Largest vessel in the bundle 20-50 +μm +. Cavities (intercellulars) between parenchyma- cells present, small, often triangular. Distinct cavities (intercellulars) in the protoxylem area of vascular bundles. + + + +Oekologie + + +Lebensform Therophyt + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + + + + + +
KEINE ANGABE
+
+
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl Fsehr trockenLichtzahl Lsehr hellSalzzeichen1
Reaktionszahl Rschwach sauer bis neutral (pH 4.5-7.5)Temperaturzahl T +sehr warm-kollin (nur an +waermsten +Stellen, Hauptverbreitung in +Suedeuropa +) +
+Naehrstoffzahl +N + +maessig +naehrstoffarm +bis +maessig +naehrstoffreich + +Kontinentalitaetszahl +K +subkontinental (niedrige relative Luftfeuchtigkeit, grosse Temperaturschwankungen, eher kalte Winter)
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Bromus madritensis +L. + + + + + + +Volksname Deutscher Name: +Madrider Trespe +Nom +francais +: +Brome de Madrid +Nome italiano: +Forasacco dei muri + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Bromus madritensis L. + + +Checklist 2017 + +66400
= +Bromus madritensis L. + + +Flora Helvetica 2001 + +2604
= +Bromus madritensis L. + + +Flora Helvetica 2012 + +2780
= +Bromus madritensis L. + + +Flora Helvetica 2018 + +2780
= +Bromus madritensis L. + + +Index synonymique 1996 + +66400
= +Bromus madritensis L. + + +Landolt 1977 + +369
= +Bromus madritensis L. + + +SISF/ISFS 2 + +66400
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Status Indigenat +: Neophyt: nach der Entdeckung von Amerika in der Region aufgetreten (nach 1500) + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein + + +
+
\ No newline at end of file diff --git a/data/38/35/6F/38356FB103AAF717ED62A56DF387EC9E.xml b/data/38/35/6F/38356FB103AAF717ED62A56DF387EC9E.xml new file mode 100644 index 00000000000..dd3b3be646a --- /dev/null +++ b/data/38/35/6F/38356FB103AAF717ED62A56DF387EC9E.xml @@ -0,0 +1,90 @@ + + + +Birds from the Azores: An updated list with some comments on species distribution + + + +Author + +Barcelos, Luis MD + + + +Author + +Rodrigues, Pedro R + + + +Author + +Bried, Joel + + + +Author + +Mendonca, Enesima P + + + +Author + +Gabriel, Rosalina + + + +Author + +Borges, Paulo Alexandre Vieira + +text + + +Biodiversity Data Journal + + +2015 + +3 + + +6604 +6604 + + + + +http://dx.doi.org/10.3897/BDJ.3.e6604 + +journal article +http://dx.doi.org/10.3897/BDJ.3.e6604 +1314-2828-3-6604 + + + + +Megaceryle alcyon (Linnaeus, 1758) + + + +Ecological interactions + +Native status +Nearctic + + + +Distribution +FLO; FAI; PIC; GRA; SJG; TER*; SMR* + + +Notes + +Occasional Migrant; Occasional Wintering. +Rodrigues et al. (2010) + + + + \ No newline at end of file diff --git a/data/38/35/7C/38357C3DFFABFFDCDB92FA1AFD78856C.xml b/data/38/35/7C/38357C3DFFABFFDCDB92FA1AFD78856C.xml new file mode 100644 index 00000000000..6ccd9a34c7c --- /dev/null +++ b/data/38/35/7C/38357C3DFFABFFDCDB92FA1AFD78856C.xml @@ -0,0 +1,397 @@ + + + +Two new species of Kiekie Polotow & Brescovit, 2018 (Araneae: Ctenidae) from the highlands of Panama + + + +Author + +Omelko, Mikhail M. + +text + + +Zootaxa + + +2023 + +2023-08-01 + + +5323 + + +2 + + +275 +284 + + + + +http://dx.doi.org/10.11646/zootaxa.5323.2.7 + +journal article +10.11646/zootaxa.5323.2.7 +1175-5326 +8204262 +D688CC7D-B01B-457D-B1B7-980BE49E5E12 + + + + + + + +Kiekie dietrichi + +sp. n. + + + + + + +( +Figs 6–10 +, +15–18 +, +23–26 +, +31–35 +, +38–39, 40–43 +) + + + + +Material examined +. + +Holotype +♁ and +paratypes +4♀ +( +ZMMU +), +PANAMA +, +Chiriquí Prov. +, +Totumas Mt. +, +8°53’3.24”N +82°40’41.05”E +, + +1900 m + +, 6– + +9.02.2022 + +( +M.M. Omelko +). + + + + + +Etymology +. The specific name is a patronym in honor of Jeffrey Dietrich (Volcan, +Panama +), the owner of the Mount Totumas Cloud Forest resort, near where the new species was collected. + + + + +Diagnosis +. Males of + +K. dietrichi + + +sp. n. + +are very similar to those of + +K. almae + + +sp. n. + +(see the diagnosis of the latter species). Both sexes of the new species are also similar to + +K. montanensis + +. Males of the new species can be easily distinguished by the large, curved RTA with a sharp tip (vs. tiny, straight, tip bifurcated; cf. +Fig. 17 +and fig. 9B in +Polotow & Brescovit 2018 +), and the females are distinguished by kidney-shaped receptacles ( +Re +) (vs. pear-shaped; cf. +Fig. 34 +and fig. 9D in +Polotow & Brescovit 2018 +). In addition, by the shape of epigyne’s median plate the female of the new species is similar to that of + +K. curvipes +( +Keyserling, 1881 +) + +, but can be easily distinguished by the small lateral tooth of epigyne ( +LT +), pointing towards each other (vs. large, pointing downwards; cf. +Figs 31–32 +and fig. 6B in +Polotow & Brescovit 2018 +). + + + + +FIGURES 27–35. +Epigyne of + +Kiekie almae + + +sp. n. + +(27–30) and + +K. dietrichi + + +sp. n. + +(31–35). 27, 31–32—intact, ventral; 28, 33—macerated, ventral; 29, 34—ditto, dorsal; 30, 35—ditto, posterior. Scale bars=0.5 mm. Abbreviations: +CD +- copulatory duct, +CO +—copulatory opening, +FD +—fertilization duct, +LT— +lateral tooth, +MP +—median plate, +Pr +—median plate projection, +Re +—receptacle. + + + + +Description. +Male ( +Figs 6–7 +, +38 +). Total length 13.01. Carapace 6.86 long, 5.33 wide. Opisthosoma 5.97 long, 4.27 wide. Coloration in ethanol. Carapace light brown, with narrow yellowish median band, diamond-shaped and 2 tiny dark spots in ocular area. Lateral bands poorly visible, wavy. Fovea thin, black. Chelicerae dark brown. Sternum brown without pattern, with dark edges. Labium brown. Endites yellowish. Dorsal part of opisthosoma light brown with poorly visible cardiac mark and number of irregular gray spots. Lateral sides yellowish with a number of gray spots, ventral part yellowish with a number of tiny gray spots. Spinnerets yellowish. Eye sizes and interdistances: AME 0.34, ALE 0.24, PME 0.40, PLE 0.31; AME–AME 0.23, AME–ALE 0.29, PME–PME 0.18, PME–PLE 0.36, AME–PME 0.11, ALE–PLE 0.12, clypeus height at AME 0.27, at ALE 0.58. + + +Leg measurements: I 25.19 (6.84, 2.78, 7.18, 6.12, 2.27), II 23.21 (6.52, 2.65, 6.38, 5.49, 2.17), III 20.69 (5.79, 2.64, 5.07, 5.12, 2.07), IV 28.53 (7.71, 2.60, 7.09, 8.51, 2.62). Femora of all legs light brown dorsally, yellowish ventrally. Other segments brown without annulation. Metatarsi IV not modified but with long lateral setae. Same setae on metatarsi III ( +Fig. 10 +). For legs spination see +Table 3 +. + + + +TABLE 3. +Palp and leg spination of male of + +Kiekie dietrichi + +sp. n. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
FePaTiMt
Leg I3d 4p 4r1p 1r2d 3p 2r 2-2-2-2-2v1p 2-2-2v
Leg II3d 4p 4r1p 1r2d 3(4)p 2r 2-2-2-2-2v0(3)p 1(2)r 2-2-2v
Leg III3d 4p 4r1p 1r3d 2p 2r 2-2-2v*1d 4p 4r 2-2-2v*
Leg IV3d 4p 2(3)r1p 1r3d 2p 2r 2-2-2v*1d 4p 4r 2-1-2-2v*
+
+ +*- segments covered with long setae especially thick on Mt IV + + +Live male with dark brown carapace (median band light brown with 2 black lateral spots anteriorly) and brown opisthosoma with a series of small black spots (see +Fig. 38 +). + + +Palp as shown in +Figs 15–18 +, +23–26 +. Tibia ca. 2.6 longer than wide, with 3 very long spines, longest ca. 0.7 of tibia length. RTA long, hook like in retrolateral view with its base near the distal edge of the tibia. Cymbium length/ width ratio ca. 2. Tip of cymbium about 0.28 of cymbial length, shorter than bulb. Subtegulum ( +St +) large, oval, almost completely hidden by embolus ( +E +) in ventral view. Sperm duct ( +SD +) clearly visible mainly in retrolateral and apical view. Median apophysis ( +MA +) comma-shaped in ventral view, cup-spahed in prolateral view, far not reaching conductor ( +C +). +MA +diagonally positioned relative to longitudinal axis of the cymbium. Conductor ( +C +) open fan-shaped, ca. 1.2 times wider than long with folded anterior edge, covering the embolus tip. +E +with wide base ( +Eb +), starting at 7 o’clock position, thin, its tip slightly curved. + + +Female ( +Figs 8–9 +, +39 +). Total length 15.74. Carapace 7.09 long, 5.30 wide. Opisthosoma 7.72 long, 5.21 wide. Carapace brown (somewhat darker than in males) with narrow yellowish median band, diamond-shaped and 2 small gray spots in ocular area. Lateral bands poorly visible, thin, divided into several spots. Fovea thin, black. Chelicerae dark brown, almost black. Sternum dark brown without pattern. Labium dark brown, almost black. Endites brown with yellowish outer edge. Dorsal part of opisthosoma dark brown with poorly visible yellowish cardiac mark and series of gray spots. Lateral part uniformly brown. Ventral part of opisthosoma dark brown with tiny gray spots and yellowish spots forming V-mark. Spinnerets brown. Eye sizes and interdistaces: AME 0.26, ALE 0.25, PME 0.43, PLE 0.36; AME–AME 0.27, AME–ALE 0.39, PME–PME 0.19, PME–PLE 0.45, AME–PME 0.18, ALE–PLE 0.20, clypeus height at AME 0.24, at ALE 0.74. + + +Leg measurements: I 18.26 (5.12, 2.43, 5.00, 3.99, 1.72), II 16.93 (4.85, 2.43, 4.47, 3.58, 1.60), III 14.69 (4.30, 1.82, 3.61, 3.39, 1.57), IV 20.35 (5.51, 1.97, 5.14, 5.80, 1.93). All legs segments brown without annulation. For legs spination see +Table 4 +. Mt and Ta I–II, Ta III–IV with dense scopula. + + + +TABLE 4. +Palp and leg spination of female of + +Kiekie dietrichi + +sp. n. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
FePaTiMt
Leg I3d 3p 3rspineless2-2-2-2-2v2-2-2v
Leg II3d 4p 2rspineless2-2-2-2-2v2-2-2v
Leg III3d 4p 4r1p 1r3d 2p 2r 2-2-2v1d 3p 3r 2-2-2v
Leg IV3d 3p 1r1p 1r2(3)d 2p 2r 2-2-2v4p 4r 2-1-2-2v
+
+ +Epigyne as shown in +Figs 31–35 +. Epigynal plate 1.3 times wider than long. Median plate ( +MP +) with 2 more or less pronounced rounded projections ( +Pr +) medially (cf. figs 31–32). Lateral teeth ( +LT +) comparatively small, well developed, triangular in ventral view, with pointed tips in posterior view. Receptacles ( +Re +) large, slightly curved. Copulatory ducts ( +CD +) short, slightly bent. Fertilization ducts ( +FD +) short, barely visible. The shape of the epigyne in + +Kiekie dietrichi + + +sp. n. + +varies widely (cf. +Figs 31–32 +). + +
+ + +Biology +. All specimens were found on the litter of primary cloud forest ( +Fig. 40–41 +). + + + + +Distribution +. +Type +locality only ( +Figs 40–43 +). + + +
+
\ No newline at end of file diff --git a/data/38/35/7C/38357C3DFFAFFFDADB92FC6AFAD18682.xml b/data/38/35/7C/38357C3DFFAFFFDADB92FC6AFAD18682.xml new file mode 100644 index 00000000000..44fb3042317 --- /dev/null +++ b/data/38/35/7C/38357C3DFFAFFFDADB92FC6AFAD18682.xml @@ -0,0 +1,99 @@ + + + +Two new species of Kiekie Polotow & Brescovit, 2018 (Araneae: Ctenidae) from the highlands of Panama + + + +Author + +Omelko, Mikhail M. + +text + + +Zootaxa + + +2023 + +2023-08-01 + + +5323 + + +2 + + +275 +284 + + + + +http://dx.doi.org/10.11646/zootaxa.5323.2.7 + +journal article +10.11646/zootaxa.5323.2.7 +1175-5326 +D688CC7D-B01B-457D-B1B7-980BE49E5E12 + + + + + + +Genus + +Kiekie +Polotow & Brescovit, 2018 + + + + + + + + +Type +species. + +Ctenus sinuatipes +F.O. +Pickard-Cambridge, 1897 + +, from +Central America +( +Panama +) + +. + + + + +Remarks. +Currently, seven species of + +Kiekie + +are known from +Panama +, including two new species described here. Almost all of them are known from both males and females, except for + +K. barrocolorado +Polotow & Brescovit, 2018 + +, which has been described based on males only. For the diagnosis and description of the genus see +Polotow & Brescovit (2018) +. The genus has a Central American distribution, except for + +K. antioquia + +, which is found in South America. + + + + \ No newline at end of file diff --git a/data/38/35/7C/38357C3DFFAFFFDEDB92FA8DFD788320.xml b/data/38/35/7C/38357C3DFFAFFFDEDB92FA8DFD788320.xml new file mode 100644 index 00000000000..1fb22cbb3f1 --- /dev/null +++ b/data/38/35/7C/38357C3DFFAFFFDEDB92FA8DFD788320.xml @@ -0,0 +1,431 @@ + + + +Two new species of Kiekie Polotow & Brescovit, 2018 (Araneae: Ctenidae) from the highlands of Panama + + + +Author + +Omelko, Mikhail M. + +text + + +Zootaxa + + +2023 + +2023-08-01 + + +5323 + + +2 + + +275 +284 + + + + +http://dx.doi.org/10.11646/zootaxa.5323.2.7 + +journal article +10.11646/zootaxa.5323.2.7 +1175-5326 +8204262 +D688CC7D-B01B-457D-B1B7-980BE49E5E12 + + + + + + + +Kiekie almae + +sp. n. + + + + + + +( +Figs 1–5 +, +11–14 +, +19–22 +, +27–30 +, +36–37, 40–43 +) + + + + +Material examined +. + +HOLOTYPE +♁ and +3♀ +paratypes +( +ZMMU +), +PANAMA +, +Chiriquí Prov. +, +Totumas Mt. +, +8°53’3.24”N +82°40’41.05”E +, + +1900 m + +, 1– + +6.02.2022 + +( +M.M. Omelko +). + + + + + +Etymology +. The specific name is a matronym in honor of Alma Dietrich, wife of Jeffrey Dietrich, the owner of the Mount Totumas Cloud Forest resort, near where the new species was collected. + + + + +Diagnosis +. Males of + +Kiekie almae + + +sp. n. + +are similar to those of + +K. dietrichi + + +sp. n. + +in having elongated, comma-shaped median apophysis, but can be easily distinguished by the strongly modified (curved) metatarsi IV (vs. unmodified; cf. +Figs 5, 10 +) and the median apophysis ( +MA +) located along the longitudinal axis of the cymbium (vs. diagonal position; cf. +Figs 20, 24 +). By general conformation of male palp and shape of epigyne’s median plate in females, the new species is also similar to + +K. panamensis +Polotow & Brescovit, 2018 + +. Males of + +K. almae + + +sp. n. + +can be easily distinguished by the RTA’s base shifted proximally from the distal edge of the palpal tibia (vs. located adjacent to the distal edge; cf. +Fig. 13 +and fig. 13B in +Polotow & Brescovit 2018 +). Females of + +K. almae + + +sp. n. + +can be distinguished from those of + +K. panamensis + +by the median plate ( +MP +), which is of equal width at the anterior and posterior edges (vs. the anterior edge significantly narrower than the posterior; cf. +Fig. 27 +and fig. 13C in +Polotow & Brescovit 2018 +). The female of the new species is also similar to that of + +K. antioquia + +but differs from it by the rounded projections ( +Pr +) of the median plate (vs. pointed) and a slightly curved posterior edge of the septum (vs. strongly curved; cf. +Fig. 27 +and fig. 14A in +Polotow & Brescovit 2018 +). + + + + +FIGURES 1–10. +General appearance (1–4, 6–9) and legs (5, 10) of + +Kiekie almae + + +sp. n. + +(1–5) and + +K. dietrichi + + +sp. n. + +(6–10). 1, 6—male, dorsal; 2, 7—ditto, ventral; 3, 8—female, dorsal; 4, 9—ditto, ventral; 5—metatarsus IV; 10—metatarsi III–IV. Scale bars: 1–4, 6–9=5 mm; 10=2mm. + + + + +Description. +Male +holotype +( +Figs 1–2, 5 +, +36 +). Total length 15.10. Carapace 7.73 long, 6.12 wide. Opisthosoma 7.35 long, 4.87 wide. Coloration in ethanol: carapace light brown, with narrow yellow median band, diamond-shaped near the ocular area. Lateral bands yellowish. Fovea thin, dark brown. Chelicerae brown, almost black. Sternum light brown without pattern. Labium light brown. Maxillae yellowish. Dorsal part of the opisthosoma with a complex pattern, consisting of a yellow cardiac mark, a pair of oblique stripes next to it, as well as a series of ca. 4 transverse stripes. Lateral sides of the opisthosoma yellow with a number of small gray spots. Ventral part yellow with some tiny grayish spots. Spinnerets uniformly yellow. Eye sizes and interdistances: AME 0.28, ALE 0.26, PME 0.42, PLE 0.41; AME–AME 0.22, AME–ALE 0.32, PME–PME 0.11, PME–PLE 0.23, AME–PME 0.12, ALE–PLE 0.18, clypeus height at AME 0.34, at ALE 0.65. + + +Leg measurements: I 34.29 (9.23, 3.35, 9.89, 8.47, 3.35), II 31.75 (8.37, 3.33, 8.95, 7.75, 3.35), III 28.33 (7.66, 2.84, 7.60, 7.48, 2.75), IV 35.94 (9.13, 3.15, 9.81, 10.18, 3.67). Femora of all legs dorsally light brown, ventrally yellow. Other segments light brown with barely visible annulation, except for metatarsi IV dark brown with light distal part, modified, strongly curved and with large spines ( +Fig. 5 +). For legs spination see +Table 1 +. + + + +TABLE 1. +Palp and leg spination of male of + +Kiekie almae + +sp. n. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
FePaTiMt
Leg I3d 3p 4r1p 1r2d 4p 3(2)r 2-2-2-2v2p 2r 2-2-2v
Leg II3d 4p 4r1p 1r2d 3(4)p 2r 2-2-2-2-2v2p 2r 2-2-2v
Leg III3d 4p 4r1p 1r2d 2p 2r 2-2-2v1d 4p 4r 2-2-2v
Leg IV3d 4p 3r1p 1r3d 2p 2r 2-2-2v2d 4p 6r 1-2v
+
+ +Living male with dark brown carapace (median band light brown) and black opisthosoma with a light brown pattern ( +Fig. 36 +). + + +Palp as shown in +Figs 11–14 +, +19–22 +. Tibia ca. 3.2 longer than wide, with 3 very long spines, longest ca. 0.67 of tibia length. RTA long, hook like with its base shifted proximally from the distal edge of the tibia. Cymbium length/width ratio ca. 1.9. Tip of cymbium about 0.3 of cymbial length, shorter than bulb. Subtegulum ( +St +) large, oval, mainly hidden by embolus ( +E +). Sperm duct ( +SD +) clearly visible mainly in retrolateral and apical view. Median apophysis ( +MA +) comma-shaped in ventral view, cup-spahed in prolateral view, not reaching conductor ( +C +). +MA +located along the longitudinal axis of the cymbium. Conductor ( +C +) open fan-shaped, ca. 1.2 times wider than long, covering the embolus tip. +E +with wide base ( +EB +), starting at 7 o’clock position, thin, with slightly curved tip. + + +Female ( +Figs 3–4 +, +37 +). Total length 20.19. Carapace 9.34 long, 7.07 wide. Opisthosoma 10.49 long, 7.12 wide. Coloration in ethanol. Carapace brown (somewhat darker than in males) with narrow yellowish median band, widened and barely visible in ocular area. Lateral bands thin, poorly visible. Fovea thin, black. Chelicerae dark brown, almost black, number of teeth like in male. Sternum light brown without pattern, with dark edges. Labium dark brown, almost black. Endites dark brown with yellow outer edges. Dorsal part of the opisthosoma with a complex pattern, consisting of a poorly visible yellow cardiac mark, a pair of small oblique stripes next to it, as well as a series of ca. 4 paired spots. Lateral sides brown with poorly visible spots, ventral brown with a few small grayish spots. Spinnerets light brown. Eye sizes and interdistances: AME 0.42, ALE 0.32, PME 0.46, PLE 0.42; AME–AME 0.27, AME–ALE 0.41, PME–PME 0.16, PME–PLE 0.52, AME–PME 0.23, ALE–PLE 0.26, clypeus height at AME 0.57, at ALE 0.95. + + +Leg measurements: I 34.16 (9.35, 4.05, 9.79, 7.85, 3.12), II 31.78 (8.74, 3.79, 8.87, 7.36, 3.02), III 28.53 (7.93, 3.33, 7.19, 7.36, 2.72), IV 36.64 (9.42, 3.46, 9.45, 10.66, 3.65). Femora of all legs brown dorsally, yellow ventrally. Other segments brown with barely visible annulation. For legs spination see +Table 2 +. + + + +TABLE 2. +Palp and leg spination of female of + +Kiekie almae + +sp. n. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
FePaTiMt
Leg I3(4) d 3p 3(4)r1r1p 1r 2-2-2-2-2v2-2-2v
Leg II3d 4p 4r1p 1r2p 1r 2-2-2-2-2v2-2-2v
Leg III3d 4p 4r1p 1r2(3)d 2p 2r 2-2-2v4p 4r 2-2-2v
Leg IV3d 3(5) p31p 1r3d 2p 2r 2-2-2v4p 6r 1-1-2-2v
+
+ + +FIGURES 11–18. +Male palp of + +Kiekie almae + + +sp. n. + +(11–14) and + +K. dietrichi + + +sp. n. + +(15–18). 11, 15—prolateral; 12, 16—ventral; 13, 17—retrolateral; 14, 18—dorsal. Scale bars=0.5 mm. Abbreviations: +RTA +—retrolateral tibial apophysis. + + + +Living female with dark brown carapace (median band brown) and black, slightly shiny opisthosoma with light brown pattern (see +Fig. 37 +). + + +Epigyne as shown in +Figs 27–30 +. Epigynal plate 1.2 times wider than long. Median plate ( +MP +) with rounded anterior edges and 2 large, rounded projections ( +Pr +) medially. Lateral teeth ( +LT +) large, well developed, slightly curved in ventral view, with pointed tips in posterior view. Receptacles ( +Re +) large, kidney-shaped. Copulatory ducts ( +CD +) slightly curved. Fertilization ducts ( +FD +) short. + +
+ + +Biology +. All specimens were found in the litter of primary cloud forest ( +Figs 40–41 +). +Notes. +The species exhibits a noticeable sexual size dimorphism, with the female being 25% larger than the male + + +(by total length). Among other species in the genus, such dimorphism is reliably known only for + +K. montanensis + +and + + + +K. panamenensis + +. +Distribution +. +Type +locality only ( +Figs 42–43 +). + + +
+
\ No newline at end of file diff --git a/data/38/35/A4/3835A4F3472DD96D638D740BCA6445C0.xml b/data/38/35/A4/3835A4F3472DD96D638D740BCA6445C0.xml new file mode 100644 index 00000000000..334f54342d8 --- /dev/null +++ b/data/38/35/A4/3835A4F3472DD96D638D740BCA6445C0.xml @@ -0,0 +1,551 @@ + + + +Advances in Legume Systematics 14. Classification of Caesalpinioideae. Part 2: Higher-level classification + + + +Author + +Bruneau, Anne +https://orcid.org/0000-0001-5547-0796 +Institut de recherche en biologie vegetale and Departement de Sciences biologiques, Universite de Montreal, 4101 Sherbrooke E., Montreal (QC) H 1 X 2 B 2, Canada +anne.bruneau@umontreal.ca + + + +Author + +de Queiroz, Luciano Paganucci +https://orcid.org/0000-0001-7436-0939 +Universidade Estadual de Feira de Santana, Departamento de Ciencias Biologicas, Av. Transnordestina s / n, Campus, Novo Horizonte. 44036 - 900, Feira de Santana, BA, Brazil + + + +Author + +Ringelberg, Jens J. +https://orcid.org/0000-0003-0567-5210 +Department of Systematic and Evolutionary Botany, University of Zurich, Zollikerstrasse 107, 8008 Zurich, Switzerland & School of Geosciences, University of Edinburgh, Old College, South Bridge, Edinburgh EH 8 9 YL, UK + + + +Author + +Borges, Leonardo M. +https://orcid.org/0000-0001-9269-7316 +Universidade Federal de Sao Carlos, Departamento de Botanica, Rodovia Washington Luis, Km 235, 13565 - 905, Sao Carlos, SP, Brazil + + + +Author + +Bortoluzzi, Roseli Lopes da Costa +https://orcid.org/0000-0002-7445-7244 +Programa de Pos-graduacao em Producao Vegetal, Universidade do Estado de Santa Catarina, Centro de Ciencias Agroveterinarias, Avenida Luiz de Camoes 2090, 88520 - 000, Lages, Santa Catarina, Brazil + + + +Author + +Brown, Gillian K. +https://orcid.org/0000-0002-7940-5435 +Queensland Herbarium and Biodiversity Science, Department of Environment and Science, Toowong, Queensland, 4066, Australia + + + +Author + +Cardoso, Domingos B. O. S. +https://orcid.org/0000-0001-7072-2656 +Instituto de Pesquisas Jardim Botanico do Rio de Janeiro, Pacheco Leao 915, 22460 - 030, Rio de Janeiro, RJ, Brazil & Programa de Pos-Graduacao em Biodiversidade e Evolucao (PPGBioEvo), Instituto de Biologia, Universidade Federal de Bahia (UFBA), Rua Barao de Jeremoabo, s. n., Ondina, 40170 - 115, Salvador, BA, Brazil + + + +Author + +Clark, Ruth P. +https://orcid.org/0000-0001-9974-2933 +Accelerated Taxonomy Department, Royal Botanic Gardens, Kew, Richmond, TW 9 3 AE, UK + + + +Author + +Conceicao, Adilva de Souza +https://orcid.org/0000-0002-8800-422X +Programa de Pos-graduacao em Diversidade Vegetal, Universidade do Estado da Bahia, Herbario HUNEB, Campus VIII, Rua do Gangorra 503, 48608 - 240, Paulo Afonso, Bahia, Brazil + + + +Author + +Cota, Matheus Martins Teixeira +https://orcid.org/0000-0003-0654-7501 +Universidade Estadual de Feira de Santana, Departamento de Ciencias Biologicas, Av. Transnordestina s / n, Campus, Novo Horizonte. 44036 - 900, Feira de Santana, BA, Brazil + + + +Author + +Demeulenaere, Else +https://orcid.org/0000-0002-1815-3051 +Center for Island Sustainability and Sea Grant, University of Guam, UOG Station, Mangilao, 96923, Guam + + + +Author + +de Stefano, Rodrigo Duno +https://orcid.org/0000-0003-1707-4121 +Centro de Investigacion Cientifica de Yucatan, A. C. (CICY), Calle 43 No. 130 x 32 y 34, Chuburna de Hidalgo; CP 97205, Merida, Yucatan, Mexico + + + +Author + +Ebinger, John E. +Eastern Illinois University, Charleston, IL 61920, USA + + + +Author + +Ferm, Julia +https://orcid.org/0000-0002-8762-3942 +Department of Ecology, Environment and Plant Sciences, 10691, Stockholm University, Stockholm, Sweden + + + +Author + +Fonseca-Cortes, Andres +https://orcid.org/0000-0001-7207-9940 +Universidade Estadual de Feira de Santana, Departamento de Ciencias Biologicas, Av. Transnordestina s / n, Campus, Novo Horizonte. 44036 - 900, Feira de Santana, BA, Brazil + + + +Author + +Gagnon, Edeline +https://orcid.org/0000-0003-3212-9688 +Department of Integrative Biology, University of Guelph, 50 Stone Road, Guelph (ON) N 1 G 2 W 1, Canada & Chair of Phytopathology, Technical University Munich, 85354 Freising, Germany & Royal Botanic Garden Edinburgh, 20 A Inverleith Row, Edinburgh, EH 3 5 LR, UK + + + +Author + +Grether, Rosaura +https://orcid.org/0000-0003-2673-665X +Departamento de Biologia, Universidad Autonoma Metropolitana-Iztapalapa, Apdo. Postal 55 - 535, 09340 Ciudad de Mexico, Mexico + + + +Author + +Guerra, Ethiene +https://orcid.org/0000-0002-9495-1717 +Universidade Federal do Rio Grande do Sul, Programa de Pos-Graduacao em Botanica, Av. Bento Goncalves 9500, Bloco IV - Predio 43433, Porto Alegre, RS, 91501 - 970, Brazil + + + +Author + +Haston, Elspeth +https://orcid.org/0000-0001-9144-2848 +Royal Botanic Garden Edinburgh, 20 A Inverleith Row, Edinburgh, EH 3 5 LR, UK + + + +Author + +Herendeen, Patrick S. +https://orcid.org/0000-0003-2657-8671 +Chicago Botanic Garden, 1000 Lake Cook Road, Glencoe, IL 60022, USA + + + +Author + +Hernandez, Hector M. +https://orcid.org/0000-0002-1741-5515 +Departamento de Botanica, Instituto de Biologia, Universidad Nacional Autonoma de Mexico, Cd. Universitaria, 04510 Ciudad de Mexico, Mexico + + + +Author + +Hopkins, Helen C. F. +https://orcid.org/0000-0003-4984-8224 +Accelerated Taxonomy Department, Royal Botanic Gardens, Kew, Richmond, TW 9 3 AE, UK + + + +Author + +Huamantupa-Chuquimaco, Isau +https://orcid.org/0000-0002-4153-5875 +Herbario Alwyn Gentry (HAG), Universidad Nacional Amazonica de Madre de Dios (UNAMAD), AV. Jorge Chavez N ° 1160, Madre de Dios, Peru + + + +Author + +Hughes, Colin E. +https://orcid.org/0000-0002-9701-0699 +Department of Systematic and Evolutionary Botany, University of Zurich, Zollikerstrasse 107, 8008 Zurich, Switzerland + + + +Author + +Ickert-Bond, Stefanie M. +https://orcid.org/0000-0001-8198-8898 +Department of Biology & Wildlife & Herbarium (ALA) at the University of Alaska Museum of the North, University of Alaska Fairbanks, P. O. Box 756960, Fairbanks AK 99775 - 6960, USA + + + +Author + +Iganci, Joao +https://orcid.org/0000-0002-5740-3666 +Universidade Federal do Rio Grande do Sul, Programa de Pos-Graduacao em Botanica, Av. Bento Goncalves 9500, Bloco IV - Predio 43433, Porto Alegre, RS, 91501 - 970, Brazil & Programa de Pos-Graduacao em Fisiologia Vegetal, Universidade Federal de Pelotas, Instituto de Biologia, Campus Universitario Capao do Leao, Passeio Andre Dreyfus, Departamento de Botanica, Predio 21, Pelotas, Rio Grande do Sul, 96010 - 900, Brazil + + + +Author + +Koenen, Erik J. M. +https://orcid.org/0000-0002-4825-4339 +Evolutionary Biology & Ecology, Universite Libre de Bruxelles, Faculte des Sciences, Campus du Solbosch - CP 160 / 12, Avenue F. D. Roosevelt, 50, 1050 Bruxelles, Belgium + + + +Author + +Lewis, Gwilym P. +https://orcid.org/0000-0003-2599-4577 +Accelerated Taxonomy Department, Royal Botanic Gardens, Kew, Richmond, TW 9 3 AE, UK + + + +Author + +de Lima, Haroldo Cavalcante +https://orcid.org/0000-0003-2154-670X +Instituto de Pesquisas Jardim Botanico do Rio de Janeiro, Pacheco Leao 915, 22460 - 030, Rio de Janeiro, RJ, Brazil & Instituto Nacional da Mata Atlantica / INMA-MCTI, Av. Jose Ruschi, 4, Centro, 29650 - 000, Santa Teresa, Espirito Santo, Brazil + + + +Author + +de Lima, Alexandre Gibau +https://orcid.org/0000-0002-9168-2507 +Instituto de Pesquisas Jardim Botanico do Rio de Janeiro, Pacheco Leao 915, 22460 - 030, Rio de Janeiro, RJ, Brazil & Department of Biological and Environmental Sciences, University of Gothenburg, Gothenburg, Sweden + + + +Author + +Luckow, Melissa +https://orcid.org/0009-0007-2543-0516 +School of Integrative Plant Science, Plant Biology Section, Cornell University, 215 Garden Avenue, Roberts Hall 260, Ithaca, NY 14853, USA + + + +Author + +Marazzi, Brigitte +https://orcid.org/0000-0003-3252-5816 +Natural History Museum of Canton Ticino, Viale C. Cattaneo 4, 6900 Lugano, Switzerland + + + +Author + +Maslin, Bruce R. +https://orcid.org/0000-0002-3039-0973 +Western Australian Herbarium, Department of Biodiversity, Conservation and Attractions, Locked Bag 104, Bentley Delivery Centre, Western Australia, 6983, Australia & Singapore Herbarium, 1 Cluny Road, Singapore, Singapore + + + +Author + +Morales, Matias +https://orcid.org/0000-0001-5540-9725 +Instituto de Recursos Biologicos, CIRN-CNIA, INTA. N. Repetto & Los Reseros s. n., Hurlingham, Buenos Aires, Argentina & Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET), Godoy Cruz 2290 (C 1425 FQB), Ciudad Autonoma de Buenos Aires, Argentina + + + +Author + +Morim, Marli Pires +https://orcid.org/0000-0003-0872-8429 +Instituto de Pesquisas Jardim Botanico do Rio de Janeiro, Pacheco Leao 915, 22460 - 030, Rio de Janeiro, RJ, Brazil + + + +Author + +Murphy, Daniel J. +https://orcid.org/0000-0002-8358-363X +Royal Botanic Gardens Victoria, Melbourne, Victoria, 3004, Australia + + + +Author + +O'Donnell, Shawn A. +https://orcid.org/0000-0003-0731-7425 +Geography and Environmental Sciences, Northumbria University, Ellison Place, Newcastle upon Tyne, NE 1 8 ST, UK + + + +Author + +Oliveira, Filipe Gomes +https://orcid.org/0000-0003-0244-3262 +Universidade Estadual de Feira de Santana, Departamento de Ciencias Biologicas, Av. Transnordestina s / n, Campus, Novo Horizonte. 44036 - 900, Feira de Santana, BA, Brazil + + + +Author + +Oliveira, Ana Carla da Silva +https://orcid.org/0000-0001-7042-5360 +Universidade Estadual de Feira de Santana, Departamento de Ciencias Biologicas, Av. Transnordestina s / n, Campus, Novo Horizonte. 44036 - 900, Feira de Santana, BA, Brazil + + + +Author + +Rando, Juliana Gastaldello +https://orcid.org/0000-0002-3714-8231 +Programa de Pos-graduacao em Ciencias Ambientais, Universidade Federal do Oeste da Bahia, Rua Professor Jose Seabra Lemos 316, 47800 - 021, Barreiras, Bahia, Brazil + + + +Author + +Ribeiro, Petala Gomes +https://orcid.org/0000-0002-0070-9971 +Universidade Estadual de Feira de Santana, Departamento de Ciencias Biologicas, Av. Transnordestina s / n, Campus, Novo Horizonte. 44036 - 900, Feira de Santana, BA, Brazil + + + +Author + +Ribeiro, Carolina Lima +https://orcid.org/0000-0001-9508-2894 +Universidade Estadual de Feira de Santana, Departamento de Ciencias Biologicas, Av. Transnordestina s / n, Campus, Novo Horizonte. 44036 - 900, Feira de Santana, BA, Brazil + + + +Author + +Santos, Felipe da Silva +https://orcid.org/0000-0002-1068-0578 +Universidade Estadual de Feira de Santana, Departamento de Ciencias Biologicas, Av. Transnordestina s / n, Campus, Novo Horizonte. 44036 - 900, Feira de Santana, BA, Brazil + + + +Author + +Seigler, David S. +https://orcid.org/0009-0003-5177-5893 +Department of Plant Biology, University of Illinois, Urbana, IL 61801, USA + + + +Author + +da Silva, Guilherme Sousa +https://orcid.org/0000-0002-4250-0017 +Instituto de Biologia, Universidade Estadual de Campinas, Campinas, 13083 - 876, Sao Paulo / SP, Brazil + + + +Author + +Simon, Marcelo F. +https://orcid.org/0000-0002-5732-1716 +Empresa Brasileira de Pesquisa Agropecuaria (Embrapa) Recursos Geneticos e Biotecnologia, Parque Estacao Biologica, Caixa Postal 02372, 70770 - 917, Brasilia / DF, Brazil + + + +Author + +Soares, Marcos Vinicius Batista +https://orcid.org/0000-0003-2660-1771 +Universidade Federal do Rio Grande do Sul, Programa de Pos-Graduacao em Botanica, Av. Bento Goncalves 9500, Bloco IV - Predio 43433, Porto Alegre, RS, 91501 - 970, Brazil + + + +Author + +Terra, Vanessa +https://orcid.org/0000-0001-5669-1304 +Instituto de Biologia, Universidade Federal de Santa Maria, 97105 - 900, Santa Maria / RS, Brazil + +text + + +PhytoKeys + + +2024 + +2024-04-03 + + +240 + + +1 +552 + + + + +http://dx.doi.org/10.3897/phytokeys.240.101716 + +journal article +http://dx.doi.org/10.3897/phytokeys.240.101716 +1314-2003-240-1 +B699D9DE2B435B1093DE3C38C703D430 + + + + +Mezcala C.E. Hughes & J.L. Contr., PhytoKeys 205: 197. 2022. + + + + +Figs 146 +, 151 + + + + +Type +. + + + +Mezcala balsensis + +(J.L. Contr.) C.E. Hughes & J.L. Contr. [≡ + +Desmanthus balsensis + +J.L. Contr.] + + + +Description. + +Unarmed multi-stemmed treelet or large shrub to 3.5 m, brachyblasts present, sheathed in persistent stipules. +Stipules +setiform with striate membranous wings. +Leaves +bipinnate, a stipitate nectary between basal pinnae pair; pinnae 2-4 (5) pairs, opposite; leaflets 8-14 pairs per pinna, oblong, opposite. +Inflorescences +capitate, 1-2 per leaf axil, composed of 30-50 functionally sterile, functionally staminate and hermaphrodite flowers, proportions of each flower type variable; bracteoles subtending each flower peltate or deltate setiform. +Flowers +with sepals and petals valvate in bud; each inflorescence with 0-5 sterile flowers proximally, staminodia filamentous, white; similar to the hermaphrodite flowers but smaller and lacking anthers and ovary; functionally staminate flowers 12-30 per inflorescence, lacking an ovary, borne above the sterile flowers; hermaphrodite flowers apical, 5-25 per inflorescence, the calyx obconic, petals 5, free, white or pale green, stamens 10, cream-white, anthers with a minute orbicular gland on a filiform stalk; pollen in tetrahedral tetrads with striate exine ornamentation; ovary sessile, glabrous, stigma narrow funnelform. +Fruits +held erect above shoots, linear-oblong, straight or weakly arcuate, terete or sub-terete, 3-10 cm long, 5-13-seeded, seeds longitudinally inserted, valves initially fleshy becoming woody or sub-woody when ripe, elastically but tardily dehiscent from the apex along both sutures (Fig. +146F, G +). +Seeds +square to rhomboidal, pleurogram deeply U-shaped, often asymmetric with unequal arms. + + + +Chromosome number. +Unknown. + + +Included species and geographic distribution. + +Monospecific ( + +M. balsensis + +), narrowly restricted, endemic in the Balsas Depression of Mexico (Fig. +151 +). + + + +Figure 151. +Distribution of + +Mezcala + +based on quality-controlled digitised herbarium records. See Suppl. material 1 for the source of occurrence data. + + + + +Ecology. + +Seasonally dry tropical forest and semi-arid thorn scrub on shallow calcareous rocky soils. Seed dispersal passive. Strongly deciduous. Nodulation status unknown. Bee-pollinated ( + +Xylocopa + +and other generalist bee species). + + + +Etymology. + +Named for the +Mezcala +culture which blossomed from 700 to 200 BC in the central Balsas Depression in Guerrero Mexico where the genus is endemic. + + + +Human uses. +Unknown. + + +Notes. + + +Mezcala + +was established as a monospecific genus to account for the non-monophyly of + +Desmanthus + +( +Hughes et al. 2022c +) by segregating the single species + +D. balsensis + +which differs from the remaining species of + +Desmanthus + +in possessing anther glands, pollen in tetrads as opposed to tricolporate monads, and erect woody, as opposed to chartaceous, fruits. + + + +Taxonomic references. + + +Contreras-Jimenez +(1986) + +including an illustration; +Hughes et al. (2022b) +; +Luckow (1993) +. + + + + \ No newline at end of file diff --git a/data/38/36/01/3836019041B99899C638005D4DA0DBC7.xml b/data/38/36/01/3836019041B99899C638005D4DA0DBC7.xml new file mode 100644 index 00000000000..2c07068fbd2 --- /dev/null +++ b/data/38/36/01/3836019041B99899C638005D4DA0DBC7.xml @@ -0,0 +1,107 @@ + + + +Synopsis of Poeciloderrhis Stal, 1874, with the description of three new species, and a redescription of the male and female of Poeciloderrhisferruginea (Brunner von Wattenwyl, 1865) from southeast Brazil (Blattodea, Blaberidae, Epilamprinae) + + + +Author + +Cardoso de Oliveira da Silva, Leonardo + + + +Author + +Lopes, Sonia Maria + +text + + +ZooKeys + + +2015 + +545 + + +53 +65 + + + + +http://dx.doi.org/10.3897/zookeys.545.6172 + +journal article +http://dx.doi.org/10.3897/zookeys.545.6172 +1313-2970-545-53 +CF78241402A3443698CE562C339AAA49 + + + +Taxon classification Animalia Blattodea Blaberidae + + + +Poeciloderrhis ferruginea (Brunner von Wattenwyl, 1865) +Figures 1-10, 11-16 + + + +General coloration. +Shiny dark brown (Figs 1 and 11). Head with vertex, interocular space between ocellar fenestra and antennae brown. Two brown spots below ocellar fenestra. Maxillary palps with brown apical segment, with golden cilia. Eyes black (Fig. 2). Pronotum semi-transparent with dark brown punctuation (Fig. 3). Tegmen semi-transparent, light brown, bearing dark brown spots. Legs light brown with spines, arolia and claws brown. Abdomen light brown with brown punctation. + + +Figures 1-10. +Poeciloderrhis ferruginea +(Brunner Von Wattenwyl, 1865) male 1 habitus 2 head, ventral view 3 pronotum, dorsal view 4 tergal modification in 1th tergite and 2th5 supra-anal plate, dorsal view 6 subgenital plate, ventral view 7 left phallomere, dorsal view 8-9 median sclerite, dorsal view 10 right phallomere. + + + + +Dimensions (male) (mm). +Total length: 32; total length of pronotum: 6.57; width of pronotum: 7.5; length of tegmen: 27.1; width of tegmen: 6.1. + + +Head. +Triangular with rounded angles, vertex hidden in dorsal view; interocular space measuring about 1 mm; antennae long, slender and tomentose, reaching beyond apex of cerci. Eyes antero-lateral in position; maxillary palps with first and second segments reduced, the second measuring 0.41 mm, third segment 25% longer than fourth and 25% shorter than fifth segment, which is a little more dilated and very tomentose. + + +Thorax. +Pronotum wide, pentagonal, convex, with curved margins, base with small median projection. Legs developed, half of femur I with anteroventral surface bearing four strong spines, followed by series of small spines towards apex, where two strong apical spines are present; posteroventral surface with three strong spines, one apical; femora II and III showing strong spaced spines on their ventral surfaces. Pulvilli present on fourth tarsal segment, claws symmetrical and specialized, with two rows of small spines on ventral surface. Tegmen reaching beyond apex of abdomen. Marginal field wide, slightly concave, convex, curved, discoidal field convex and short at apex, anal field convex and well-marked. + + +Abdomen. +Tergal modification pyramid-shaped, tall, with cilia, located on first tergite and depression followed by curved stalk on second tergite (Fig. 4). Supra-anal plate round with cerci reaching beyond the plate (Fig. 5). Subgenital plate asymmetric, with two slender styles, one long, and one short; larger style with sharper lateral tomentosity (Fig. 6). Left phallomere with median structure shaped as sclerotized cleft (Fig. 7). Median apical sclerite spiniform with intense sclerotization, with membranous sclerotized structure bearing lateral shaft and slender pre-apical structure (Figs 8, 9). Right phallomere with straight apex and a small spine next to apex; lateral portion of phallomere with spines (Fig. 10). + + +Dimensions (female) (mm). +Total length: 33.5; total length of pronotum: 7.7; width of pronotum: 9.45; length of tegmen: 29.3; width of tegmen: 7.8. Female larger than male; brown color of vertex extending to frons (Fig. 12); pronotum brown; in the abdomen, anal plate enlarged with indistinct slit medially, cerci poorly developed reaching apex of plate (Fig. 14); subgenital plate triangular (Fig. 15); female genitalia in three pairs of valves, of which the first is the most developed and widens toward apex, the second is the smallest and most sclerotized, and the third is more slender apically and slightly smaller in length than the first. Valvifers tapered and very small (Fig. 16). + + +Figures 11-16. +Poeciloderrhis ferruginea +(Brunner Von Wattenwyl, 1865) female. 11 habitus 12 head, ventral view 13 pronotum, dorsal view 14 supra-anal plate, dorsal view 15 subgenital plate, ventral view; 16 valves, dorsal view. + + + + +Material examined. + +1 ♂ Brazil, Minas Gerais, Catas Altas, RPPN Serra da +Caraca +, collected at 1490 m; 3 to 7/XII/ 2013. J. P. Botero, A. Carelli & G. C. Queiroz cols; 1 ♀ Brazil, data the same as for male. + + + +Diagnosis. + +The male of +Poeciloderrhis ferruginea +differs from the male in the size of the body, brown color of the vertex extending to the frons; enlarged supra-anal plate with indistinct median indentation, cerci poorly developed reaching apex of the plate; subgenital plate triangular; female genitalia with 3 pairs of valves; valvifers slender and small. + + + + \ No newline at end of file diff --git a/data/38/36/03/3836035ADCD4BB538A188476F48DCF5D.xml b/data/38/36/03/3836035ADCD4BB538A188476F48DCF5D.xml new file mode 100644 index 00000000000..4201af37424 --- /dev/null +++ b/data/38/36/03/3836035ADCD4BB538A188476F48DCF5D.xml @@ -0,0 +1,195 @@ + + + +Order Chiroptera - Family Vespertilionidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +451 +529 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Vespadelus +Troughton 1943 + + + + + + + +Vespadelus +Troughton 1943 + +, + +Furred animals of +Australia +, 1st ed., Sydney: Angus and Robertson: 349 + + +. + + + + +Type Species: + +Scotophilus pumilus +Gray 1841 + + + + + +Synonyms: + +Registrellus +Troughton 1943 + +. + + + + +Species and subspecies: +9 species: + + +Species + +Vespadelus baverstocki +Kitchener, Jones, and Caputi 1987 + + + +Species + +Vespadelus caurinus +(Thomas 1914) + + + +Species + +Vespadelus darlingtoni +(G. M. +Allen 1933 +) + + + +Species + +Vespadelus douglasorum +Kitchener 1976 + + + +Species + +Vespadelus finlaysoni +Kitchener, Jones, and Caputi 1987 + + + +Species + +Vespadelus pumilus +(Gray 1841) + + + +Species + +Vespadelus regulus +(Thomas 1906) + + + +Species + +Vespadelus troughtoni +Kitchener, Jones, and Caputi 1987 + + + +Species + +Vespadelus vulturnus +(Thomas 1914) + + + + + +Discussion: + +Vespadelus + +was first published as a +nomen nudum +(no accompanying diagnosis) by +Iredale and Troughton (1934) +; the name was made available by Troughton (1943), who provided a diagnosis. Often included in + +Pipistrellus + +(e.g., +Hill and Harrison, 1987 +) or + +Eptesicus + +(e.g., +Adams et al., 1987 +; Kitchener et al., 1987; +Koopman, 1993 +, +1994 +; McKean et al., 1978), but see +Volleth and Tidemann (1991) +and +Volleth and Heller (1994) +. Revised by Kitchener et al. (1987); see also +Adams et al. (1987) +and +Queale (1997) +. Species groups follow Kitchener et al. (1987). + + + + \ No newline at end of file diff --git a/data/38/36/FA/3836FAB92DEECF4AFDE2AED2AD5D70ED.xml b/data/38/36/FA/3836FAB92DEECF4AFDE2AED2AD5D70ED.xml new file mode 100644 index 00000000000..85188be30bb --- /dev/null +++ b/data/38/36/FA/3836FAB92DEECF4AFDE2AED2AD5D70ED.xml @@ -0,0 +1,80 @@ + + + +Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea + + + +Author + +Dale-Skey, Natalie + + + +Author + +Askew, Richard R. + + + +Author + +Noyes, John S. + + + +Author + +Livermore, Laurence + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8013 +8013 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8013 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8013 +1314-2828-4-8013 + + + + +Seladerma genale (Thomson, 1876) + + + + +Lamprotatus genalis +Thomson, 1876 + + + +Notes + +Identification uncertain ( +Graham (1969a) +, based on a male specimen + + + + \ No newline at end of file diff --git a/data/38/37/28/3837287A9DA65545A88BE975D9FF9122.xml b/data/38/37/28/3837287A9DA65545A88BE975D9FF9122.xml new file mode 100644 index 00000000000..9b3473ac93d --- /dev/null +++ b/data/38/37/28/3837287A9DA65545A88BE975D9FF9122.xml @@ -0,0 +1,91 @@ + + + +Distribution patterns of Chinese Cixiidae (Hemiptera, Fulgoroidea), highlight their high endemic diversity + + + +Author + +Luo, Yang +Key Laboratory of Plant Protection Resources and Pest Management, Ministry of Education, Entomological Museum, College of Plant Protection, Northwest A & F University, Yangling, Shaanxi 712100, China, Yangling, China + + + +Author + +Bourgoin, Thierry +https://orcid.org/0000-0001-9277-2478 +Institut de Systematique, Evolution, Biodiversite, ISYEB-UMR 7205, MNHN-CNRS-Sorbonne Universite-EPHE-Univ. Antilles, Museum national d'Histoire naturelle, CP 50, 57 rue Cuvier, F- 75005, Paris, France +thierry.bourgoin@mnhn.fr + + + +Author + +Zhang, Jia-Lin +Key Laboratory of Plant Protection Resources and Pest Management, Ministry of Education, Entomological Museum, College of Plant Protection, Northwest A & F University, Yangling, Shaanxi 712100, China, Yangling, China + + + +Author + +Feng, Ji-Nian +Key Laboratory of Plant Protection Resources and Pest Management, Ministry of Education, Entomological Museum, College of Plant Protection, Northwest A & F University, Yangling, Shaanxi 712100, China, Yangling, China +jinianf@nwsuaf.edu.cn + +text + + +Biodiversity Data Journal + + +2022 + +2022-01-24 + + +10 + + +75303 +75303 + + + + +http://dx.doi.org/10.3897/BDJ.10.e75303 + +journal article +http://dx.doi.org/10.3897/BDJ.10.e75303 +1314-2828-10-e75303 +07802C19F192544C9F561556F25CA5C4 + + + + +Oecleopsis articara Van Stalle, 1991 + + + + +Oecleopsis articara +Van Stalle, 1991: 22.| Guo et al., 2009: 48. + + + +Distribution + +China: Hainan, Henan, Sichuan ( +Guo et al. 2009 +), Guizhou; Malaysia: Borneo, Pahang ( +Van Stalle 1991 +). + + + +Notes +New record: China: Guizhou (Duyun). This species is recorded here from China only based on female specimens. + + + \ No newline at end of file diff --git a/data/38/37/84/383784915C095E3DB4EBDFEBAE9B3954.xml b/data/38/37/84/383784915C095E3DB4EBDFEBAE9B3954.xml new file mode 100644 index 00000000000..ef5f634b286 --- /dev/null +++ b/data/38/37/84/383784915C095E3DB4EBDFEBAE9B3954.xml @@ -0,0 +1,237 @@ + + + +Taxonomic revision of the Pheidole sikorae species group (Hymenoptera, Formicidae) from Madagascar + + + +Author + +Salata, Sebastian +Department of Entomology, California Academy of Sciences, San Francisco, CA 94118, USA +https://orcid.org/0000-0003-0811-2309 +sdsalata@gmail.com + + + +Author + +Fisher, Brian L. +Department of Entomology, California Academy of Sciences, San Francisco, CA 94118, USA +https://orcid.org/0000-0002-4653-3270 + +text + + +ZooKeys + + +2020 + +949 + + +1 +185 + + + + +http://dx.doi.org/10.3897/zookeys.949.51269 + +journal article +http://dx.doi.org/10.3897/zookeys.949.51269 +1313-2970-949-1 +93BFA448BB7343CDBC4EA86090DA63D5 +303D64593B3B550DBB7CE01AA547409D + + + + +Pheidole sparsa +sp. nov. +Figs 55A-F +, 64M +, 67E + + + +Type material. + +Holotype. +Madagascar. • 1 major worker; Mahajanga; Region Sofia, Bemanevika; +-14.337 +, +48.58874 +; alt. 1606 m; 14 Jan 2015; B. L. Fisher et al. leg.; montane rainforest, ex rotten log; BLF35640; CASENT0705586 (CASC). +Paratype. +• 1w.; same data as for holotype; CASENT0923289 (CASC). + + + +Figure 55. + +Pheidole sparsa + +sp. nov., full-face view ( +A +), profile ( +C +), and dorsal view ( +E +) of paratype minor worker (CASENT0923289) and full-face view ( +B +), profile ( +D +), and dorsal view ( +F +) of holotype major worker (CASENT0705586). + + + + +Other material. + +Madagascar. - +Mahajanga +: •1w., 1s.; Region Sofia, Bemanevika; +-14.337 +, +48.58874 +; alt. 1606 m; 14 Jan 2015; B. L. Fisher et al. leg.; montane rainforest, ex rotten log; BLF35624 (CASC). • 1w., 1s.; Region Sofia, Bemanevika; +-14.337 +, +48.58874 +; alt. 1606 m; 14 Jan 2015; B. L. Fisher et al. leg.; montane rainforest, ex rotten log; BLF35664 (CASC). • 1w., 1s.; Region Sofia, Bemanevika; +-14.337 +, +48.58874 +; alt. 1606 m; 15 Jan 2015; B. L. Fisher et al. leg.; montane rainforest, ex rotten log; BLF35713 (CASC). + + + +Diagnosis. + +Moderately large species. +Major workers. +Head in full-face view sub-oval, not widening posteriorly, with anterior and posterior sides relatively straight, in lateral view sub-oval; ventral and dorsal faces convex; sides of the head with dense, moderately long, suberect to erect pilosity; medial part of frons with moderately sparse, thick, longitudinal, and interrupted rugae, rugae in posteromedial slightly directed outward, interspaces shiny with sparse and indistinct rugofoveolae; anterolateral sides with longitudinal, thick, and relatively sparse rugae; posterolateral sides with irregular, thick, and relatively sparse rugae; interspaces shiny with sparse and indistinct rugofoveolae; occipital lobes and area posterolateral from eyes without smooth notches; scape, when laid back, exceeding the midlength of head by two-fifths of its length; inner hypostomal teeth distinct, large, closely spaced, triangular, with rounded apex directed upward; outer hypostomal teeth lobe-like, approximately the same height and width as inner hypostomal teeth, apex directed outward; inner and outer hypostomal teeth closely spaced and not connected by concavity; promesonotum predominantly smooth, with indistinct rugofoveolae on lateral sides; katepisternum rugofoveolate with smooth notch; propodeum rugofoveolate; gaster smooth; body dark orange. +Minor workers. +Head foveolate; medial part of frons with smooth notch and indistinct, short rugulae; area posterolateral from eyes predominantly smooth; scape, when laid back, surpassing the posterior head margin by one-fifth of its length; promesonotum moderately low and moderately long, arched; promesonotal groove absent; propodeal spines small and triangular; pronotum with very indistinct and sparse foveolae; mesonotum, anepisternum, katepisternum, and propodeum smooth; body dark yellow. + + + +Description. + +Major workers. +Measurements ( +N += 4): HL: 0.94-1.13 (1.06); HW: 0.94-1.1 (1.04); SL: 0.61-0.72 (0.67); EL: 0.12-0.14 (0.13); WL: 0.93-1.0 (0.98); PSL: 0.16-0.2 (0.18); MTL: 0.6-0.65 (0.62); PNW: 0.41-0.5 (0.45); PTW: 0.14-0.18 (0.16); PPW: 0.27-0.32 (0.3); CI: 99.0-103.0 (101.7); SI: 62.7-65.5 (64.7); PSLI: 15.9-17.5 (16.7); PPI: 45.2-61.7 (53.9); PNI: 42.6-45.4 (43.6); MTI: 55.9-64.7 (59.4). + + +Head. +In full-face view sub-oval, not widening posteriorly, with anterior and posterior sides relatively straight (Fig. +55B +). In lateral view sub-oval; ventral and dorsal faces convex; inner hypostomal teeth visible. Sides of the head with dense, moderately long, erect pilosity; whole head with dense, long, decumbent to erect pilosity. Medial part of frons with moderately sparse, thick, longitudinal, and interrupted rugae, posteromedial rugae slightly directed outward, interspaces shiny with sparse and indistinct rugofoveolae; anterolateral sides with longitudinal, thick, and relatively sparse rugae; posterolateral sides with irregular, thick, and relatively sparse rugae; interspaces shiny with sparse and indistinct rugofoveolae. Occipital lobes with sparse, thick, and irregular rugae; interspaces smooth. Gena with relatively sparse, thick, and longitudinal rugae and smooth interspaces. Area posterolateral from eyes with thin and dense rugofoveolae and smooth interspaces. Centre of clypeus smooth and shiny, lateral sides with indistinct rugulae; median notch present, moderately wide, and shallow; median longitudinal carina absent; lateral longitudinal carinae absent. Scape, when laid back, exceeding the midlength of head by two-fifths of its length; pilosity subdecumbent to erect (Fig. +55B, D +). Inner hypostomal teeth distinct, large, closely spaced, triangular, with rounded apex directed upward; outer hypostomal teeth lobe-like, approximately the same height and width as inner hypostomal teeth, apex directed outward; inner and outer hypostomal teeth closely spaced and not connected by concavity (Fig. +64M +). +Mesosoma. +In lateral view, promesonotum short, angular, and moderately low, posterior mesonotum moderately steep, mesonotal process indistinct, tubercle-like; promesonotal groove absent; metanotal groove indistinct; propodeal spines moderately long, moderately narrow, with acute apex; humeral area laterally weakly produced (Fig. +55D +). Surface shiny; promesonotum predominantly smooth, with indistinct rugofoveolae on lateral sides; katepisternum rugofoveolae with smooth notch; propodeum rugofoveolate. Pilosity relatively dense, long, and erect (Fig. +55D, F +). +Petiole. +Shiny with fine and sparse rugofoveolae; node smooth, low, triangular, with rounded and thin apex, in rear view node dorsoventrally slightly convex; pilosity moderately sparse and erect (Fig. +55D, F +). +Postpetiole. +Shiny and smooth; in dorsal view oval, lateral margins medially with two dentate projections; pilosity long, moderately sparse, and erect (Fig. +55D, F +). +Gaster. +Shiny and smooth; pilosity moderately dense, long, and erect (Fig. +55D, F +). +Colour. +Dark orange; mandibles and gaster slightly darker; legs yellowish (Fig. +55D, F +). + + +Minor workers. +Measurements ( +N += 4): HL: 0.59-0.6 (0.59); HW: 0.49-0.52 (0.51); SL: 0.58-0.66 (0.62); EL: 0.09-0.11 (0.1); WL: 0.7-0.73 (0.72); PSL: 0.08-0.1 (0.09); MTL: 0.47-0.52 (0.49); PNW: 0.34-0.35 (0.34); PTW: 0.08-0.1 (0.09); PPW: 0.14-0.15 (0.14); CI: 116.0-119.6 (117.1); SI: 115.0-133.4 (123.3); PSLI: 14.0-16.2 (15.4); PPI: 53.1-69.9 (63.1); PNI: 65.3-69.6 (67.6); MTI: 92.9-102.4 (97.9). + + +Head. +Cephalic margin indistinctly convex or straight (Fig. +55A +). Pilosity relatively sparse, long, decumbent to suberect. Sculpture foveolate; medial part of frons with smooth notch and indistinct, short rugulae; area posterolateral from eyes predominantly smooth. Clypeus with median longitudinal carina absent; two lateral longitudinal carinae absent. Scape, when laid back, surpassing the posterior head margin by one-fifth of its length; pilosity dense, subdecumbent to erect (Fig. +55A, C +). +Mesosoma. +In lateral view, promesonotum moderately low and moderately long, arched; promesonotal groove absent; metanotal groove distinct; propodeal spines small and triangular (Fig. +55C +). Pronotum with very indistinct and sparse foveolae; mesonotum, anepisternum, katepisternum, and propodeum smooth. Pilosity very sparse, moderately long, and erect (Fig. +55C, E +). +Postpetiole. +Short, low, and relatively flat; with few short, erect setae (Fig. +55C, E +). +Gaster. +With sparse, erect pilosity (Fig. +55C, E +). +Colour. +Dark yellow, vertex and gaster slightly darker (Fig. +55C, E +). + + + +Etymology. +Latin for sparse in reference to sparse rugae on the frons. + + +Biology. +The species was collected at 1606 m in elevation, in montane rainforest. Nests were located in rotten logs. + + +Comments. + + +Pheidole sparsa + +sp. nov., described from Bemanevika in Mahajanga, is most similar to + +P. dasos + +sp. nov., known from Makirovana forest in Antsiranana, and + +P. hazo + +sp. nov., recorded so far only from the vicinity of Andranoma in Antananarivo. Majors of + +P. sparsa + +sp. nov. can be distinguished from both taxa mentioned above by medial part of frons with moderately sparse rugae, interspaces with sparse and indistinct rugofoveolae, and predominantly smooth promesonotum with indistinct rugofoveolae on lateral sides; minors of + +P. sparsa + +sp. nov. can be distinguished from + +P. hazo + +sp. nov. by dark yellow body colouration and propodeum with indistinct and sparse foveolae, and from + +P. dasos + +sp. nov. by dark yellow body colouration, shorter scape surpassing the posterior head margin by one-fifth of its length, and pronotum with very indistinct and sparse foveolae. + + + + \ No newline at end of file diff --git a/data/38/38/11/383811825A0752C0AAE9F1613B6F3461.xml b/data/38/38/11/383811825A0752C0AAE9F1613B6F3461.xml new file mode 100644 index 00000000000..f1fe1242d84 --- /dev/null +++ b/data/38/38/11/383811825A0752C0AAE9F1613B6F3461.xml @@ -0,0 +1,122 @@ + + + +A generic classification of Xenidae (Strepsiptera) based on the morphology of the female cephalothorax and male cephalotheca with a preliminary checklist of species + + + +Author + +Benda, Daniel +https://orcid.org/0000-0002-5729-0411 +Department of Zoology, Faculty of Science, Charles University, Prague, Czech Republic & Department of Entomology, National Museum, Prague, Czech Republic +benda.daniel@email.cz + + + +Author + +Pohl, Hans +https://orcid.org/0000-0002-7090-6612 +Institut fuer Zoologie und Evolutionsforschung, Friedrich-Schiller-Universitaet, Jena, Germany + + + +Author + +Nakase, Yuta +Department of Biology, Faculty of Science, Shinshu University, Matsumoto, Japan + + + +Author + +Beutel, Rolf +Institut fuer Zoologie und Evolutionsforschung, Friedrich-Schiller-Universitaet, Jena, Germany + + + +Author + +Straka, Jakub +https://orcid.org/0000-0002-8987-1245 +Department of Zoology, Faculty of Science, Charles University, Prague, Czech Republic + +text + + +ZooKeys + + +2022 + +2022-04-07 + + +1093 + + +1 +134 + + + + +http://dx.doi.org/10.3897/zookeys.1093.72339 + +journal article +http://dx.doi.org/10.3897/zookeys.1093.72339 +1313-2970-1093-1 +23B7070849A94681AC20494D06F98CCE +D3A8D50FF61A5B61B8776D63EB0D3F4C + + + + +Sphecixenos abbotti (Pierce, 1909) +comb. nov. + + + + +Homilops abbotti +Pierce, 1909: 147. + + +Pseudoxenos abbotti +(Pierce, 1909) (new combination by +Bohart 1937 +). + + +Paraxenos abbotti +(Pierce, 1909) (new combination by +Kinzelbach 1971b +). + + + +Host. + + +Sphex + +sp. (as + +Proterosphex + +sp.) ( +Pierce 1909 +). + + + +Distribution. + +Thailand: Trang ( +Pierce 1909 +). + + + + \ No newline at end of file diff --git a/data/38/38/1D/38381DC69A3C84A72A0D6B37A56F484A.xml b/data/38/38/1D/38381DC69A3C84A72A0D6B37A56F484A.xml new file mode 100644 index 00000000000..1df128b6662 --- /dev/null +++ b/data/38/38/1D/38381DC69A3C84A72A0D6B37A56F484A.xml @@ -0,0 +1,172 @@ + + + +Flora Helvetica - Rosaceae + + + +Author + +Konrad Lauber + + + +Author + +Gerhart Wagner + + + +Author + +Andreas Gygax + +text + + +2018 +Haupt Verlag + +Bern + + + +Flora Helvetica + + + +234 +314 + + + +book chapter +978-3-258-08047-5 + + + + + +Rosa uriensis +(Christ) Puget + + + + + +Artbeschreibung: Stacheln leicht +gekruemmt +bis fast gerade, +Teilblaetter +doppelt +gezaehnt +, ziemlich klein, etwas voneinander entfernt, meist behaart. Blattstiele stets behaart, mit +Stieldruesen +und Stacheln. + +Bluetenstiele +kahl, kurz, wie die +Kelchblaetter +mit +Stieldruesen +. Griffel wollig behaart. +Kelchblaetter +nach dem +Bluehen +abstehend oder aufgerichtet + +, bis zur Fruchtreife bleibend. + + + + +Bluetezeit +: 6-7 + + +Standort und Verbreitung in der Schweiz: Lichtes +Gebuesch +, trockene +Haenge +/ montan-subalpin / A + + + + +Verbreitung global: +Europaeisch + + + + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +maessig +trocken +Lichtzahl LhellSalzzeichen--
Reaktionszahl Rschwach sauer bis neutral (pH 4.5-7.5)Temperaturzahl Tunter-subalpin und ober-montan
+Naehrstoffzahl +N + +maessig +naehrstoffarm +bis +maessig +naehrstoffreich + +Kontinentalitaetszahl +K +subkontinental (niedrige relative Luftfeuchtigkeit, grosse Temperaturschwankungen, eher kalte Winter)
+
+
+ + +Volksname Deutscher Name: +Uri-Rose +Nom +francais +: +Rosier d'Uri +Nome italiano: + +Rosa d'Uri + + + +
+
\ No newline at end of file diff --git a/data/38/38/77/383877D7E6EA69D8908A3CD26B0174B9.xml b/data/38/38/77/383877D7E6EA69D8908A3CD26B0174B9.xml new file mode 100644 index 00000000000..7d9dc58071f --- /dev/null +++ b/data/38/38/77/383877D7E6EA69D8908A3CD26B0174B9.xml @@ -0,0 +1,65 @@ + + + +A key to Camponotus Mayr of Australia. + + + +Author + +McArthur, A. J. + +text + + +Memoirs of the American Entomological Institute + + + +Editor + +Snelling, R. R. + + + +Editor + +Fisher, B. L. + + + +Editor + +Ward, P. S. + + +2007 + +Advances in ant systematics (Hymenoptera: Formicidae): Homage to E. O. Wilson - 50 years of contributions. + + +80 + + +290 +351 + + + + +http://hdl.handle.net/10199/15375 + +journal article +21285 + + + + +Camponotus inflatus Lubbock + + + +Worker. HW 1.3 - 2.4; HL 1.5 - 2.3; PW 1.25 - 1.6. Black; matte; plentiful erect setae on all surfaces; anterior clypeal margin median section mostly straight. Major worker. Head sides convex; vertex concave. Minor worker. Head sides straight tapering forward; vertex mostly straight; propodeum dorsum slightly convex. + + + \ No newline at end of file diff --git a/data/38/38/C3/3838C3C29F722223E5A294AEBB824D9E.xml b/data/38/38/C3/3838C3C29F722223E5A294AEBB824D9E.xml new file mode 100644 index 00000000000..3078cbbad31 --- /dev/null +++ b/data/38/38/C3/3838C3C29F722223E5A294AEBB824D9E.xml @@ -0,0 +1,100 @@ + + + +The ants collected by the American Museum Congo Expedition. + + + +Author + +Wheeler, W. M. + +text + + +Bulletin of the American Museum of Natural History + + +1922 + +45 + + +39 +269 + + + + +http://plazi.org:8080/dspace/handle/10199/17097 + +journal article +20597 + + + + +Psalidomyrmex obesus +, +new species + + + +Text Figure 19 +Worker.- Length nearly 12 mm. + +Very similar to +procerus +but differing in the following characters: the body is distinctly more robust, the head being rectangular, and without the mandibles as broad as long, the thorax with more rounded surfaces and a swollen appearance. The mandibles are like those of +procerus +but slightly broader at the angle between the basal and apical borders and the tips are less curved. The antennal scapes reach the posterior corners of the head; funicular joints 3 to 8 as long as broad, 9 and 10 slightly longer than broad. On the thorax the mesoepinotal suture is more distinct than in +procerus +and there is a narrow median longitudinal furrow on the posterior half of the pronotum as well as on the base of the epinotum. The petiole in profile is much shorter and higher and, seen from above, much broader in proportion to its length than in +procerus +, being very distinctly broader than long, flat and truncated posteriorly, more rounded in front, with the anteroventral tooth long and rather acute. + + + +Fig, 19. +Psalidomyrmex obesus +, +new species +. Worker. a, head from above; b, thorax and abdomen in profile. + + + +The sculpture differs from that of +procerus +as follows: the longitudinal rugae covering the mandibles are distinctly coarser, the surface of the head and thorax is more opaque, the foveola; being somewhat smaller, shallower and less shining, though about as numerous and the striolae of the interfoveolar surface less sharp. The petiole and postpetiole are smoother and more shining than the head and thorax unci the interfoveolar sculpture is so feeble as to appear more or less coriaceous or alutaceous. The first gastric segment is longitudinally, not arcuately striolate. The femora are transversely, the scapes and tibiae longitudinally striolate as in +procerus +. + +Erect hairs somewhat more numerous on the dorsal surface of the head and pronotum and on the antennal scapes. + +Nearly coal black, darker than +procerus +, legs, excluding the coxa;, mandibles, clypeus, frontal carinae, antennae, and terminal gastric segments castaneous as in +procerus +. + + + + + +Described from two specimens from Medje from the stomach of a toad (Bufo superciliaris) collected by Lang and Chapin. This form is certainly distinct and is, in my opinion, more than a subspecies of +procerus +. + + + + + + +Map 15. Distribution of the genus +Leptogenys +. This genus also occurs in Georgia. + + + + + \ No newline at end of file diff --git a/data/38/38/D0/3838D085228265497AF924DEE5893426.xml b/data/38/38/D0/3838D085228265497AF924DEE5893426.xml new file mode 100644 index 00000000000..8f8a079f7ac --- /dev/null +++ b/data/38/38/D0/3838D085228265497AF924DEE5893426.xml @@ -0,0 +1,83 @@ + + + +Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea + + + +Author + +Dale-Skey, Natalie + + + +Author + +Askew, Richard R. + + + +Author + +Noyes, John S. + + + +Author + +Livermore, Laurence + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8013 +8013 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8013 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8013 +1314-2828--8013 + + + + +Anagrus bakkendorfi Soyka, 1946 + + + + +latipennis +Soyka, 1956 + + + +Distribution +England + + +Notes + +Added by +Triapitsyn and Berezovskiy (2004) + + + + \ No newline at end of file diff --git a/data/38/39/B6/3839B65DC3660D16327E759DA4FB90B2.xml b/data/38/39/B6/3839B65DC3660D16327E759DA4FB90B2.xml new file mode 100644 index 00000000000..e50ac3b63a7 --- /dev/null +++ b/data/38/39/B6/3839B65DC3660D16327E759DA4FB90B2.xml @@ -0,0 +1,75 @@ + + + +Cyanobacteria of Greece: an annotated checklist + + + +Author + +Gkelis, Spyros + + + +Author + +Ourailidis, Iordanis + + + +Author + +Panou, Manthos + + + +Author + +Pappas, Nikos + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +10084 +10084 + + + + +http://dx.doi.org/10.3897/BDJ.4.e10084 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e10084 +1314-2828-4-10084 + + + + + +Dolichospermum spiroides (Klebhan) Wacklin, L. Hoffmann & +Komarek +, 2009 + + + + + +Anabaena spiroides + + + +Notes + +Anagnostidis 1968 + + + + \ No newline at end of file diff --git a/data/38/3A/00/383A002E602AF23ADB6D516863801473.xml b/data/38/3A/00/383A002E602AF23ADB6D516863801473.xml new file mode 100644 index 00000000000..a117735480d --- /dev/null +++ b/data/38/3A/00/383A002E602AF23ADB6D516863801473.xml @@ -0,0 +1,110 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part A) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +252 +342 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Aloe + +hyacinthoides Linnaeus var. +zeylanica +Linnaeus, + +Species Plantarum +1 + +: 321. 1753 + + + + +. + + + + +"Habitat +α +in Zeylona." RCN: 2504. + + + + +Basionym of: + +Aletris hyacinthoides +(L.) L. var. +zeylanica +(L.) L. (1753) + +. + + + + +Lectotype +(Wijnands in +Taxon +22: 109. 1973): [icon] + +" +Aloe Zeylanica +pumila foliis variegatis" + +in Commelin, Hort. Med. Amstelod. Pl. Rar. 2: 41, t. 21. 1701. + + + + +Current name: + + +Sansevieria zeylanica + +(L.) Willd. + +( +Agavaceae +/ +Liliaceae +). + + + + \ No newline at end of file diff --git a/data/38/3A/45/383A45DB7D47CDA9F65C572967BAFB62.xml b/data/38/3A/45/383A45DB7D47CDA9F65C572967BAFB62.xml new file mode 100644 index 00000000000..080676c940c --- /dev/null +++ b/data/38/3A/45/383A45DB7D47CDA9F65C572967BAFB62.xml @@ -0,0 +1,84 @@ + + + +Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea + + + +Author + +Dale-Skey, Natalie + + + +Author + +Askew, Richard R. + + + +Author + +Noyes, John S. + + + +Author + +Livermore, Laurence + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8013 +8013 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8013 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8013 +1314-2828--8013 + + + + + +Astichus +Foerster +, 1856 + + + + + +CLOSTEROCEROIDES +Girault, 1913 + + +CLOSTEROMPHALE +Girault & Dodd, 1915 + + +CLOSTEROMYIIA +Girault, 1920 + + + + \ No newline at end of file diff --git a/data/38/3A/4D/383A4D0D745A5EFDB2412886E29EA86A.xml b/data/38/3A/4D/383A4D0D745A5EFDB2412886E29EA86A.xml new file mode 100644 index 00000000000..931f644dbd1 --- /dev/null +++ b/data/38/3A/4D/383A4D0D745A5EFDB2412886E29EA86A.xml @@ -0,0 +1,58 @@ + + + +Checklist of British and Irish Hymenoptera - Braconidae + + + +Author + +Broad, Gavin R. + + + +Author + +Shaw, Mark R. + + + +Author + +Godfray, H. Charles J. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8151 +8151 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8151 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8151 +1314-2828--8151 + + + + +Phaenocarpa (Phaenocarpa) notabilis Stelfox, 1944 + + + +Distribution +Scotland, Ireland + + + \ No newline at end of file diff --git a/data/38/3A/87/383A87EC3807FFEC4ADBFF3EE474BFE3.xml b/data/38/3A/87/383A87EC3807FFEC4ADBFF3EE474BFE3.xml new file mode 100644 index 00000000000..ed00e3ad16a --- /dev/null +++ b/data/38/3A/87/383A87EC3807FFEC4ADBFF3EE474BFE3.xml @@ -0,0 +1,144 @@ + + + +Five new species of Qadria Mahmood (Hemiptera: Cicadellidae: Typhlocybinae) from China + + + +Author + +Song, Yue-Hua + + + +Author + +Li, Zi-Zhong + +text + + +Zootaxa + + +2014 + +3760 + + +3 + + +439 +448 + + + +journal article +46522 +10.11646/zootaxa.3760.3.10 +14495be1-03fc-4415-87b2-c09af665ae46 +1175-5326 +226910 +DEA100C9-3FA6-4F4A-8C2A-26A806A43452 + + + + + + +5. + +Qadria cucullata + +sp. nov. + + + + + + +( +Figs. 34–42 +; m–o) + + +Description. +Body length male 3.1–3.2 mm. Body (Fig. m) brownish yellow. Head ( +Figs. 34 +, m) significantly narrower than pronotum, anterior margin angulately produced. Crown ( +Fig. 34 +, m) with round red preapical spot medially, and other little dark spots around it. Eyes (Figs. m–o) black. Face (Fig. o) long and narrow, anteclypeus and 4/5 of frontoclypeus brownish yellow, rest of frontoclypeus whitish yellow, with two ivory yellow preapical streaks. Pronotum ( +Figs. 34 +, m) with anterior margin milky yellow, median part and posterior margin darker, yellowish brown. Mesonotum ( +Figs. 34 +, m), almost as long as length of pronotum. Fore wing ( +Figs. 35 +, m, n) yellowish white, with two longitudinal red stripes, outer (4th) apical cell very small. + + +Abdominal apodemes ( +Fig. 36 +) extremely small, not extended beyond hind margin of 3rd sternite. + + + +FIGURES 34–42. + +Qadria cucullata + +Song & Li +sp. nov. +34. Head and thorax, dorsal view; 35. Fore wing; 36. Abdominal apodemes; 37. Male pygofer lobe, lateral view; 38. Subgenital plate; 39. Style; 40. Aedeagus, lateral view; 41. Aedeagus, ventral view; 42. Connective. + + + +Male genitalia. +Pygofer lobe ( +Fig. 37 +) broad, with rounded caudal margin, several long macrosetae grouped at basal lower angle, short rigid microsetae situated near caudal margin on inner surface, sparse long fine setae and well developed microtrichia on lateral surface. Pygofer dorsal appendage ( +Fig. 37 +) with line of weakness at base but not movably articulated with pygofer lobe, narrowing towards apex, slightly curved ventrad. Anal tube ( +Fig. 37 +) with basal processes, tapering towards apex. Subgenital plate ( +Fig. 38 +) distinctly widened subbasally, several short peglike setae forming continuous row along upper margin, 3 basal macrosetae on outer surface, apex pocketlike. Style ( +Fig. 39 +) with two pointed apex short, toothlike. Aedeagus ( +Figs. 40, 41 +) with pair of processes arising from base of shaft ventrally, much shorter than shaft. Preatrium long, with large single basal process, extended ventrad. Dorsal apodeme short. Gonopore ( +Figs. 40, 41 +) subapical, ventral. Connective ( +Fig. 42 +) U-shaped. + + +Specimens examined. +Holotype +♂: +China +, Guizhou Prov., Bijie, Bailidujuan, +15 October 2007 +, coll. Qiongzhang Song. +Paratypes +: 2♂♂, same data as +holotype +. + + + + +Diagnosis. +This species can be distinguished from all the other species by its aedeagus having a single process on the preatrium and a pair of basal processes which are shorter than the shaft, and by the small spoon-shaped abdominal apodemes. + + + + +Etymology. +The specific epithet is derived from the Latin word “ +cucullatus +” referring to the small spoonshaped abdominal apodemes characteristic for this species. + + + + \ No newline at end of file diff --git a/data/38/3A/87/383A87EC3809FFE24ADBFB4EE3C3BC11.xml b/data/38/3A/87/383A87EC3809FFE24ADBFB4EE3C3BC11.xml new file mode 100644 index 00000000000..8d38e58677a --- /dev/null +++ b/data/38/3A/87/383A87EC3809FFE24ADBFB4EE3C3BC11.xml @@ -0,0 +1,121 @@ + + + +Five new species of Qadria Mahmood (Hemiptera: Cicadellidae: Typhlocybinae) from China + + + +Author + +Song, Yue-Hua + + + +Author + +Li, Zi-Zhong + +text + + +Zootaxa + + +2014 + +3760 + + +3 + + +439 +448 + + + +journal article +46522 +10.11646/zootaxa.3760.3.10 +14495be1-03fc-4415-87b2-c09af665ae46 +1175-5326 +226910 +DEA100C9-3FA6-4F4A-8C2A-26A806A43452 + + + + + + +4. + +Qadria guiyanga + +sp. nov. + + + + + + +( +Figs. 25–33 +; j–l) + + +Description. +Body length male 2.8 mm. Dorsum (Figs. J–l) milk yellow. Head ( +Figs. 25 +, j) slightly narrower than pronotum, anterior margin angulately produced medially. Crown and pronotum with symmetrical orange red spots. Eyes (Figs. J–l) blackish grey. Face (Fig. l) long and narrow, brownish yellow, several orange red stripes scattered at lower part of clypeus and above antennae. Mesonotum ( +Figs. 25 +, j) with red apex, basal triangles brownish, with red streaks around its margin. Fore wing ( +Figs. 26 +, j, k) brownish white, with darkened apex, with several orange red patches and some other small light brown spots. + + +Abdominal apodemes ( +Fig. 27 +) extending to anterior margin of 4th sternite. + + +Male Genitalia. +Pygofer lobe ( +Fig. 28 +) broad, with several long macrosetae at basal lower angle and sparse long fine setae, short rigid macrosetae near caudal margin on inner surface. Pygofer dorsal appendage ( +Fig. 28 +) immovably fused with pygofer lobe, but with line of weakness at base, bifurcate near apex, slightly expanded basally. Anal tube ( +Fig. 28 +) with process concave apically. Subgenital plate ( +Fig. 29 +) long, wide basally, tapering towards apex, acutely narrowed subapically, (maybe, not fully developed in studied specimen), numerous short rigid setae uniseriate along upper margin, 3 long macrosetae situated on outer surface. Style ( +Fig. 30 +) with apex truncate. Aedeagus ( +Figs. 31, 32 +) complex, with three pairs of appendages and one unpaired process; one pair arising near apex dorsally and has serrated anterior margin, processes are flattened and look like bird wings in ventral view; single short toothlike process extended on the same level with previous appendages on ventral side of aedeagal shaft; two ventral pairs of appendages: short pair at base of shaft and long pair (much longer than shaft) on preatrium. Preatrium quite short, dorsal apodeme short, slightly expanded in lateral view. Gonopore ( +Figs. 31, 32 +) apical, ventral. Connective ( +Fig. 33 +) U-shaped. + + +Specimens examined. +Holotype +♂: +China +, Guizhou Prov., Guiyang, Longdongbao, at light, +23 June 2008 +, coll. Can Li. + + + + +Diagnosis. +This species can be distinguished from all the other species by the unique aedeagus with three pairs of appendages and a single toothlike process on the ventral side of the aedeagal shaft. +Etymology. +The specific epithet is named for the +type +locality, Guiyang, Guizhou Prov. + + + + \ No newline at end of file diff --git a/data/38/3A/87/383A87EC3809FFE34ADBFF3EE3C3B9B0.xml b/data/38/3A/87/383A87EC3809FFE34ADBFF3EE3C3B9B0.xml new file mode 100644 index 00000000000..ed76e4594d4 --- /dev/null +++ b/data/38/3A/87/383A87EC3809FFE34ADBFF3EE3C3B9B0.xml @@ -0,0 +1,142 @@ + + + +Five new species of Qadria Mahmood (Hemiptera: Cicadellidae: Typhlocybinae) from China + + + +Author + +Song, Yue-Hua + + + +Author + +Li, Zi-Zhong + +text + + +Zootaxa + + +2014 + +3760 + + +3 + + +439 +448 + + + +journal article +46522 +10.11646/zootaxa.3760.3.10 +14495be1-03fc-4415-87b2-c09af665ae46 +1175-5326 +226910 +DEA100C9-3FA6-4F4A-8C2A-26A806A43452 + + + + + + +3. + +Qadria dongfanga + +sp. nov. + + + + + + +( +Figs. 16–24 +; g–i) + + +Description. +Body length male 2.2–2.3 mm. Dorsum (Fig. g) yellow or milk yellow. Head ( +Figs. 16 +, g) slightly narrower than pronotum, anterior margin angulately produced medially, coronal suture short, extending to 1/3 of vertex. Crown ( +Figs. 16 +, g) with large leaflike orange yellow spot. Eyes ( +Figs. 16 +, g, h) blackish grey. Face (Fig. i) light brown, with darkened areas below antennal pits, frontoclypeus milky yellow medially. Pronotum ( +Figs. 16 +, g) broad, with large irregular orange yellow patches medially and two brown spots situated near lateral edges, anterior margin whitish yellow, hind margin and median area brownish. Mesonotum ( +Figs. 16 +, g) with single triangular orange yellow spot apically, basal triangles orange yellow. Fore wing ( +Figs. 17 +, g) yellowish white, with several orange yellow stripes. + + +Abdominal apodemes ( +Fig. 18 +) slightly broadened, reaching anterior margin of 5th sternite. + + +Male genitalia. +Pygofer lobe ( +Fig. 19 +) broad, with several long macrosetae at basal lower angle, numerous distinct microtrichia scattered at dorsoapical area, and with several short setae near caudal margin on inner surface. Pygofer dorsal appendage ( +Fig. 19 +) immovably fused to pygofer with a line of weakness at base, not extended beyond pygofer apex, straight in lateral view. Anal tube process ( +Fig. 19 +) long, with weak twist near apex. Subgenital plate ( +Fig. 20 +) broadened subbasally, with distinct marginal rigid setae forming continuous row, three long basal macrosetae arising near medial constriction section. Style ( +Fig. 21 +) with apex expanded, second point slightly short, toothlike. Aedeagus ( +Figs. 22, 23 +) with pair of apical processes, processes forked near base with long branches, single fingerlike process arising at tip of the aedeagus and extended dorsad. Aedeagal shaft ( +Fig. 22 +) bent dorsad in lateral view, dorsal apodeme slightly longer than preatrium. Gonopore ( +Figs. 22, 23 +) terminal, ventral. Connective ( +Fig. 24 +) V-shaped. + + +Specimens examined. +Holotype +♂: +China +, Hainan Prov., Datian Nature Reserve, +9 July 2007 +, coll. Bin Zhang. +Paratypes +: 1♀, same data as +holotype +. + + + + +Diagnosis. +The new species is similar to + +Qadria erythromaculata +Ramakrishnan & Menon, (1973) + +, sharing similar terminal processes of the aedeagus and lacking long basal processes. It can be distinguished from the latter by the bifurcation of the distal aedeagal processes, the angulate pygofer lobe and the stem of connective extremely short. + + + + +Etymology. +The specific epithet is named for the +type +locality, Dongfang, Hainan Prov. + + + + \ No newline at end of file diff --git a/data/38/3A/87/383A87EC380CFFE04ADBF9D1E33EBC4A.xml b/data/38/3A/87/383A87EC380CFFE04ADBF9D1E33EBC4A.xml new file mode 100644 index 00000000000..b58c9579413 --- /dev/null +++ b/data/38/3A/87/383A87EC380CFFE04ADBF9D1E33EBC4A.xml @@ -0,0 +1,148 @@ + + + +Five new species of Qadria Mahmood (Hemiptera: Cicadellidae: Typhlocybinae) from China + + + +Author + +Song, Yue-Hua + + + +Author + +Li, Zi-Zhong + +text + + +Zootaxa + + +2014 + +3760 + + +3 + + +439 +448 + + + +journal article +46522 +10.11646/zootaxa.3760.3.10 +14495be1-03fc-4415-87b2-c09af665ae46 +1175-5326 +226910 +DEA100C9-3FA6-4F4A-8C2A-26A806A43452 + + + + + + +2. + +Qadria daliensis + +sp. nov. + + + + + + +( +Figs. 9–15 +; d–f) + + +Description. +Body length male 3.3 mm; female 3.4–3.6 mm. Head ( +Fig. 9 +, d) slightly narrower than pronotum, anterior margin angulately produced medially. Crown ( +Fig. 9 +, d) sordid brown, with two milky preapical spots. Coronal suture (Fig. 1) distinct, extended nearly to half of vertex. Eyes ( +Fig. 9 +, d) blackish grey. Face (Fig. f) with anteclypeus and frontoclypeus brownish yellow, gena with blackish brown spat under antennal pit, other areas of gena yellowish white. Pronotum ( +Fig. 9 +, d) broad, concolorous with vertex, with darker, black brown middle part and posterior margin. Mesonotum ( +Fig. 9 +, d), sordid brown. Basal triangles concolorous with rest of mesonotum. Fore wing ( +Fig. 10 +, d) brownish white, its apex darker, with several large orange red or orange yellow markings. + + + +FIGURES 9–15. + +Qadria daliensis + +Song & Li +sp. nov. +9. Head and thorax, dorsal view; 10. Fore wing; 11. Male pygofer lobe, lateral view; 12. Subgenital plate; 13. Style; 14. Aedeagus and connective, lateral view; 15. Aedeagus and connective, ventral view. + + + +Male genitalia. +Pygofer lobe ( +Fig. 11 +) broad, with several long macrosetae at basal lower angle and sparse long fine setae, short macrosetae scattered around caudal magin on inner surface. Pygofer dorsal appendage ( +Fig. 11 +) immovably fused to margin of pygofer lobe, with a basal line of weakness, expanded basally, with twisted dorsal edge subapically near apex, apex pointed. Anal tube ( +Fig. 11 +) with basal processes bifurcate apically, ventral posterior branch little longer than dorsal anterior branch. Subgenital plate ( +Fig. 12 +) distinctly broadened, with several stout setae in distinct group subbasally, pocketlike at apex, 4 basal macrosetae on lateral surface, other numerous marginal peglike short microsetae forming continuous row. Style ( +Fig. 13 +) with apex expanded, second point short. Aedeagus ( +Figs. 14, 15 +) with two pairs of processes arising from base and apex of shaft respectively: apical pair short, extended ventrad; basal pair very long, much longer than shaft, with small rounded impressions distally. Preatrium short, but longer than dorsal apodeme. Gonopore ( +Figs. 14, 15 +) apical. Connective ( +Fig. 15 +) about U-shaped. + + +Specimens examined. +Holotype +♂: +China +, Yunnan Prov., Dali, Erhai, +4 August 2006 +, coll. Zaihua Yang. +Paratypes +: 3♀♀, +China +, Yunnan Prov., Lanping, +8 August 2006 +, coll. Qiongzhang Song. + + + + +Diagnosis. +The male genital apparatus of the new species is similar to that of + +Qadria cajanae +Ahmed (1971) + +, but can be distinguished from the latter by the reduced dorsal apodeme, broad aedeagal shaft in lateral view; pronotum without V- or Y-shaped dark patch medially. + + + + +Etymology. +The specific epithet is named for the +type +locality, Dali, Yunnan Prov. + + + + \ No newline at end of file diff --git a/data/38/3A/87/383A87EC380EFFE44ADBFE7AE2C3B83A.xml b/data/38/3A/87/383A87EC380EFFE44ADBFE7AE2C3B83A.xml new file mode 100644 index 00000000000..4785d4edb18 --- /dev/null +++ b/data/38/3A/87/383A87EC380EFFE44ADBFE7AE2C3B83A.xml @@ -0,0 +1,276 @@ + + + +Five new species of Qadria Mahmood (Hemiptera: Cicadellidae: Typhlocybinae) from China + + + +Author + +Song, Yue-Hua + + + +Author + +Li, Zi-Zhong + +text + + +Zootaxa + + +2014 + +3760 + + +3 + + +439 +448 + + + +journal article +46522 +10.11646/zootaxa.3760.3.10 +14495be1-03fc-4415-87b2-c09af665ae46 +1175-5326 +226910 +DEA100C9-3FA6-4F4A-8C2A-26A806A43452 + + + + + + +Key to males of the genus + +Qadria + + + + + + + + +1 Aedeagus with pair of long ventral processes at base of shaft.................................................. ··2 + + +- Aedeagus without pair of long ventral processes at base of shaft (sometimes with single one)........................ 12 + + + + +2 Aedeagal shaft without additional shorter processes.......................................................... 3 + + +- Aedeagal shaft with additional shorter processes............................................................ ·6 + + + + + +3 Aedeagal shaft broad terminally in posterior view................................... + +Q. rubronotata +( +Distant, 1918 +) + + + + +- Aedeagal shaft narrow terminally in posterior view.......................................................... 4 + + + + + +4 Dorsal apodeme of aedeagus well developed............................................. + +Q. setosa +( +Ahmed, 1970 +) + + + + +- Dorsal apodeme of aedeagus not distinct.................................................................. ·5 + + + + + +5 Pygofer with posterior margin truncated, aedeagal shaft long and slender in lateral view... + +Q. tandojamensis +( +Ahmed, 1969 +) + + + + + +- Pygofer with posterior margin angulated, aedeagal shaft short and wide in lateral view...... + +Q. pakistanica +( +Ahmed, 1969 +) + + + + + + +6 Aedeagal shaft with pair of apical processes................................................................ 7 + + +- Aedeagal shaft without pair of apical processes............................................................. 11 + + + + +7 Apical processes of aedeagal shaft extending ventrad......................................................... 8 + + +- Apical processes of aedeagal shaft extending laterad or dorsad................................................. 10 + + + + + +8 Pronotum without Y-shaped dark patch medially ( +Fig. 9 +)............................. + +Q. daliensis + +Song & Li +sp. nov. + + + +- Pronotum with Y-shaped dark patch medially.............................................................. ·9 + + + + + +9 Terminal part of long basal processes of aedeagus transversely striated...................... + +Q. cajanae +( +Ahmed, 1971 +) + + + + + +- Terminal part of long basal processes of aedeagus distinctly twisted.......... + +Q. palniensis +( +Ramakrishnan & Menon, 1973 +) + + + + + + + +10 Dorsal wall of gonopore with short sclerotized protrusion............................ · + +Q. plamista +Dworakowska, 1981 + + + + + +- Dorsal wall of gonopore without sclerotized protrusion (Fig. 7)....................... + +Q. bannaensis + +Song & Li +sp. nov. + + + + + + +11 Aedeagal shaft with pair of short basal processes ventrally ( +Figs. 31, 32 +)................· + +Q. guiyanga + +Song & Li +sp. nov. + + + + +- Aedeagal shaft with pair of short subpical processes ventrally........................... + +Q. bella +Dworakowska, 1981 + + + + + + + +12 Aedeagus with single large preatrial appendage ( +Figs. 40, 41 +)..........................· + +Q. cucullata + +Song & Li +sp. nov. + + + +- Aedeagus without preatrial appendage.................................................................... 13 + + + + + +13 Apical processes of aedeagus bifurcate ( +Figs. 22, 23 +)............................... + +Q. dongfanga + +Song & Li +sp. nov. + + + + +- Apical processes of aedeagus not bifurcate......................... + +Q. erythromaculata +( +Ramakrishnan & Menon, 1973 +) + + + + + + + \ No newline at end of file diff --git a/data/38/3A/87/383A87EC380EFFE74ADBFAC3E34EBA55.xml b/data/38/3A/87/383A87EC380EFFE74ADBFAC3E34EBA55.xml new file mode 100644 index 00000000000..54cdcdcd6d5 --- /dev/null +++ b/data/38/3A/87/383A87EC380EFFE74ADBFAC3E34EBA55.xml @@ -0,0 +1,140 @@ + + + +Five new species of Qadria Mahmood (Hemiptera: Cicadellidae: Typhlocybinae) from China + + + +Author + +Song, Yue-Hua + + + +Author + +Li, Zi-Zhong + +text + + +Zootaxa + + +2014 + +3760 + + +3 + + +439 +448 + + + +journal article +46522 +10.11646/zootaxa.3760.3.10 +14495be1-03fc-4415-87b2-c09af665ae46 +1175-5326 +226910 +DEA100C9-3FA6-4F4A-8C2A-26A806A43452 + + + + + + +1. + +Qadria bannaensis + +sp. nov. + + + + + +(Figs. 1–8; a–c) + +Description. +Body length male 2.0–2.1 mm; female 2.1–2.2 mm. Head (Fig. 1, a) slightly narrower than pronotum, its anterior margin angulately produced medially. Crown (Fig. 1, a) light yellow, with irregular blackish brown spots, with color lightening towards apex, becoming reddish at transition to face. Eyes (Fig. 1, a) blackish grey. Face (Fig. c) with whole anteclypeus and 2/3 of frontoclypeus orange-yellow, upper 1/3 of frontoclypeus sordid brown, with ivory-white patches near apex. Pronotum (Fig. 1, a) broad, light yellow, slightly wider than long, with large brown or blackish brown patches medially. Mesonotum (Fig. 1, a), concolorous with crown, with basal triangles and apex blackish brown, transverse impression short and distinct, slightly curved. Fore wing (Fig. 2, a) brownish white, with darker apex and several large orange red, orange yellow, or reddish brown markings. + +Abdominal apodemes (Fig. 3) extending to hind margin of 4th sternite. + +Male genitalia. +Pygofer lobe (Fig. 4) broad, with several long macrosetae at basal lower angle and sparse long fine setae, few short rigid microsetae scattered near caudal magin on internal surface. Pygofer dorsal appendage (Fig. 4) with distinct line of weakness at base, but not movably articulated with pygofer lobe, bifurcate apically, dorsal branch extremely long, bent ventrad, more than 2 times longer than ventral branch. Anal tube process (Fig. 4) with truncate apex. Subgenital plate (Fig. 5) with lateral margin distinctly widened subbasally, several short peglike setae in distinct group subbasally, apex of plate pocketlike, and 3 basal macrosetae on outer surface. Style (Fig. 6) with apex expanded, second point long and tapering apically. Aedeagus (Figs. 7, 8) with two pairs of processes arising from base and apex of shaft respectively: apical pair short and straight, extended laterad; basal pair very long, much longer than shaft. Aedeagal shaft short, preatrium and dorsal apodeme slightly expanded. Gonopore (Fig. 8) at apex. Connective (Fig. 8) nearly Y-shaped. + + +Specimens examined. +Holotype +♂: +China +, Yunnan Prov., Xishuangbanna, Virgin forest Park, +21 July 2008 +, coll. Yuehua Song. +Paratypes +: +1♂ +, 3♀♀, same data as +holotype +. + + + + +Diagnosis. +The new species resembles + +Qadria palniensis +Ramakrishnan & Menon (1973) + +, but can be distinguished from the latter by the terminal aedeagal processes extending laterad and long ventral basal processes not twisted apically, and the stem of the connective short. + + + + +Etymology. +The specific epithet is named for the +type +locality, Xishuangbanna, Yunnan Prov. + + +FIGURES a–o. +a–c, + +Qadria bannaensis + +Song & Li +sp. nov. +; d–f, + +Q. daliensis + +Song & Li +sp. nov. +; g–i, + +Q. dongfanga + +Song & Li +sp. nov. +; j–l, + +Q. guiyanga + +Song & Li +sp. nov. +; m–o, + +Q. cucullata + +Song & Li +sp. nov. +. + + + + \ No newline at end of file diff --git a/data/38/3A/87/383A87EC380FFFE44ADBFA0EE43CBCA6.xml b/data/38/3A/87/383A87EC380FFFE44ADBFA0EE43CBCA6.xml new file mode 100644 index 00000000000..a09ed263dcc --- /dev/null +++ b/data/38/3A/87/383A87EC380FFFE44ADBFA0EE43CBCA6.xml @@ -0,0 +1,124 @@ + + + +Five new species of Qadria Mahmood (Hemiptera: Cicadellidae: Typhlocybinae) from China + + + +Author + +Song, Yue-Hua + + + +Author + +Li, Zi-Zhong + +text + + +Zootaxa + + +2014 + +3760 + + +3 + + +439 +448 + + + +journal article +46522 +10.11646/zootaxa.3760.3.10 +14495be1-03fc-4415-87b2-c09af665ae46 +1175-5326 +226910 +DEA100C9-3FA6-4F4A-8C2A-26A806A43452 + + + + + + + +Qadria +Mahmood + + + + + + + + + +Qadria + +Mahmood, 1967 +: 18 + + + + + + + +Type +species: + +Empoasca rubronotata +Distant, 1918 + + +Spatulostylus +Ramakrishnan & Menon, 1973 +: 16 + +Type +species: + +Spatulostylus variegatus +Ramakrishnan & Menon, 1973 + + + + + +Description. +Dorsum yellow or white, with red, orange or brown color pattern. Head as wide or slightly narrower than pronotum. Crown fore margin strongly produced and angulate medially. Vertex unicolorous, sometimes with pale preapical spots or dark submedial lines, often with lateral branch. Pronotum pale or dark medially or with Y- or V-shaped medial vitta. Fore wing usually with orange or reddish spots, or broken oblique vittae. + +Male basal abdominal apodemes small to long, rounded apically. Anal tube with paired basolateral processes extended ventrad into genital capsule. + +Pygofer lobe rounded or angulate. Pygofer dorsal appendage with line of weakness at base, but not moveable. Macrosetae at basal lower angle of pygofer in distinct group, microtrichia well developed. Subgenital plate widened subbasally, with several basal macrosetae (except in + +Q. tandojamensis +Ahmed + +, plate reduced, without macrosetae). Style with two pointed apex, preapical lobe prominent. Aedeagus usually with pair of long ventral processes at the base; some species with apical or subapical processes. Preatrium short, dorsal apodeme short or slightly expanded. Connective nearly Y-shaped, median anterior lobe absent, two arms long, stem short or reduced. + + + + +Diagnosis +. The most important features separating + +Qadria + +from related genera are as follows: pygofer dorsal appendage immovably fused to dorsal margin, basolateral setae in distinct group; aedeagus ventral processes placed basally, well separated from shaft, longer than shaft (some individual species without ventral processes, but with apical processes); connective median anterior lobe absent. Style with two pointed apex. + + + + +Distribution: +Oriental and Southeastern Palearctic regions. + + + + \ No newline at end of file diff --git a/data/38/3A/87/383A87F0FFB9FFB9FF2E7840FCBC3284.xml b/data/38/3A/87/383A87F0FFB9FFB9FF2E7840FCBC3284.xml new file mode 100644 index 00000000000..b259cff29f9 --- /dev/null +++ b/data/38/3A/87/383A87F0FFB9FFB9FF2E7840FCBC3284.xml @@ -0,0 +1,132 @@ + + + +New Records of Corylophidae (Coleoptera) from the Maritime Provinces of Canada + + + +Author + +Majka, Christopher G. + + + +Author + +Cline, Andrew R. + +text + + +The Coleopterists Bulletin + + +2006 + +2006-06-30 + + +60 + + +2 + + +105 +111 + + + + +http://dx.doi.org/10.1649/864.1 + +journal article +10.1649/864.1 +1938-4394 + + + + + + + +Clypastrea lunata +(LeConte) + + + + + + + +NOVA SCOTIA +: +Guysborough County +: + +Trafalgar +, + +19 July 1992 + +, +2 specimens +, +S. & J. Peck +, +JCC + +; + + +Queens County +: + +Medway River +, + +13 July 1993 + +, +3 specimens +, +J. & T. Cook +, +JCC + +. + + + + +Newly recorded in Nova Scotia and in +Canada +as a whole; in the +U.S.A. +recorded from +Maine +(Dearborn and Donahue 1993), +New Hampshire +, +Massachusetts +( +Chandler 2001 +), +Connecticut +, +New York +, +Indiana +, +Florida +, and +Missouri +(Downie and Arnett 1996). +Sikes (1998) +also reports the species from +Rhode Island +. In Nova Scotia all specimens were collected in flight in the evening with a car net. + + + + \ No newline at end of file diff --git a/data/38/3A/87/383A87F0FFB9FFB9FF2E7B45FF6E318C.xml b/data/38/3A/87/383A87F0FFB9FFB9FF2E7B45FF6E318C.xml new file mode 100644 index 00000000000..b6c536f0cbc --- /dev/null +++ b/data/38/3A/87/383A87F0FFB9FFB9FF2E7B45FF6E318C.xml @@ -0,0 +1,156 @@ + + + +New Records of Corylophidae (Coleoptera) from the Maritime Provinces of Canada + + + +Author + +Majka, Christopher G. + + + +Author + +Cline, Andrew R. + +text + + +The Coleopterists Bulletin + + +2006 + +2006-06-30 + + +60 + + +2 + + +105 +111 + + + + +http://dx.doi.org/10.1649/864.1 + +journal article +10.1649/864.1 +1938-4394 + + + + + + + +Clypastrea lugubris +(LeConte) + + + + + + + +NOVA SCOTIA +: +Colchester County +: + +Masstown +, + +7 June 1990 + +, +T.D. Smith +, +NSNR + +; + +Debert +, + +19 June 1993 + +, +J. Ogden +, +NSNR + +; + + +Halifax County +: + +Antrim +, + +2 May 2005 + +, +J. Ogden +, +2 specimens +, +NSNR + +; + +Upper Musqudoboit +, + +31 August 1999 + +, +J. Ogden +, +NSNR + +; + + +Pictou County +: + +Sheepherders Junction +, + +15 June 2004 + +, +J. Ogden +& +N. Wood +, +NSNR + +. + + + + + +Recorded in +Canada +from the +Yukon +east to +Ontario +Campbell (1991) +; in the U.S.A. from New York and Michigan (Downie and Arnett 1996). Newly recorded in Nova Scotia + +. + + + + \ No newline at end of file diff --git a/data/38/3A/87/383A87F0FFB9FFBEFF2E7949FEC031A6.xml b/data/38/3A/87/383A87F0FFB9FFBEFF2E7949FEC031A6.xml new file mode 100644 index 00000000000..dd037cd3e31 --- /dev/null +++ b/data/38/3A/87/383A87F0FFB9FFBEFF2E7949FEC031A6.xml @@ -0,0 +1,427 @@ + + + +New Records of Corylophidae (Coleoptera) from the Maritime Provinces of Canada + + + +Author + +Majka, Christopher G. + + + +Author + +Cline, Andrew R. + +text + + +The Coleopterists Bulletin + + +2006 + +2006-06-30 + + +60 + + +2 + + +105 +111 + + + + +http://dx.doi.org/10.1649/864.1 + +journal article +10.1649/864.1 +1938-4394 + + + + + + + +Sericoderus lateralis +(Gyllenhal) + + + + + + + +NOVA SCOTIA +: +Cape Breton County +: + +Sydney +, + +5 October 2003 + +, +C.W. D’Orsay +, mixed forest, +CBU + +; + + +Kings County +: + +Kentville +, + +10 August 2005 + +, +D.H. Webster +, compost, +DHWC + +; +Pictou + + + + +County: + +Lyons Brook, + +26 August 2002 + +, +E. Georgeson +, +NSNR + +. + + +In +Canada +recorded from +British Columbia +and +Québec +( +Campbell 1991 +); in the +U.S.A. +scattered records from +Maine +( +Chandler 2001 +) and +Massachusetts +south to +Florida +and west to +Washington +(Downie and Arnett 1996). This is an adventive Palearctic species, which in Europe is broadly distributed across the continent ( + +Freude +et al. +1971 + +). Bowestead and Leschen (2002) report that members of + +Sericoderus + +feed on Hypomycetes and Zygomycetes and can be found in bird and caterpillar nests. In Nova Scotia found feeding on moldy corncobs in a compost heap. In Europe it occurs, often in very large numbers, on moldy plant remains in warm places, especially garden compost and grass cuttings ( +Bowestead 1999 +). + + +This species was first reported in North America in +Oregon +in 1949 (as + +Arthrolips decolor +(LeConte)) + +in the nest of a woodrat (Walters and Roth 1950). Meagre past collecting for this family makes it difficult to establish if this species has recently spread to the province or if it has existed undetected for some time. Newly recorded in +Nova Scotia +. + + + +Orthoperinae + +Orthoperus suturalis +LeConte + + + + + + +NEW BRUNSWICK +: +Albert County +: + +Mary’s Pt. +, + +12 August 2004 + +, sea shore, +C.G. Majka +, +CGMC + +. + + +NOVA SCOTIA +: +Cape Breton County +: + +Sydney Tar +ponds, + +16–22 July 1996 + +, +P.A. Rankin +, +CBU + +; + + +Guysborough County +: + +George Lake +, + +15–30 June 1997 + +, +D.J. Bishop +, +NSMC + +; + +Malay Lake +, + +2–15 June 1997 + +, +D.J. Bishop +, +NSMC + +; + + +Halifax County +: + +Moser lake +, + +1–16 July 1997 + +, +D.J. Bishop +, +NSMC + +; + + +Hants County +: + +Little Armstrong Lake +, + +14 May–2 June 1997 + +, +D.J. Bishop +, +NSMC + +; + +Armstrong Lake +, + +2–15 June 1997 + +, +D.J. Bishop +, +NSMC + +; + + +Kings County: + +Coldbrook +, + +30 June 2002 + +, +C.G. Majka +, +3 specimens +, +CGMC + +; + +Kentville +, + +15 November 2002 + +, +D.H. Webster +, +DHWC + +; + + +Queens County +: + +Kejimkujik National Park +, + +15 August 2001 + +, +B. Wright +, +2 specimens +, +NSMC + +; + +Alma Lake +, + +22 May 2003 + +, +P. Dollin +, +NSMC + +; + + +Yarmouth County +: + +Quinlan +: +Coldstream Rd. +, + +19 July 1993 + +, +J. & T. Cook +, +JCC + +. + + + + +PRINCE EDWARD ISLAND +: +Queens County +: + +Pinette +, + +24 June 2003 + +, +C.G. Majka +, +4 specimens +, +CGMC + +; + +Millvale +: +Trout River +, + +25 June 2003 + +, +C.G. Majka +, +4 specimens +, +CGMC + +; + +Harrington +, + +25 July 2005 + +, +M.E.M Smith +, +ACPE + +. + + + +In +Canada +recorded from +Ontario +( +Campbell 1991 +); in the United States from New York, Michigan, and Florida (Downie and Arnett 1996). Newly recorded in Nova Scotia and +Prince Edward Island +. Collected from sphagnum bogs, red spruce ( + +Picea rubens +Sarg. + +) forests of all ages, +and deciduous forests by sweep and car netting and with flight-intercept traps + +. + + + + \ No newline at end of file diff --git a/data/38/3A/87/383A87F0FFBBFFB9FF2E7F00FD19308B.xml b/data/38/3A/87/383A87F0FFBBFFB9FF2E7F00FD19308B.xml new file mode 100644 index 00000000000..07f07945e34 --- /dev/null +++ b/data/38/3A/87/383A87F0FFBBFFB9FF2E7F00FD19308B.xml @@ -0,0 +1,335 @@ + + + +New Records of Corylophidae (Coleoptera) from the Maritime Provinces of Canada + + + +Author + +Majka, Christopher G. + + + +Author + +Cline, Andrew R. + +text + + +The Coleopterists Bulletin + + +2006 + +2006-06-30 + + +60 + + +2 + + +105 +111 + + + + +http://dx.doi.org/10.1649/864.1 + +journal article +10.1649/864.1 +1938-4394 + + + + + + + +Clypastrea fuscum +Harold + + + + + + + +NOVA SCOTIA +: +Queens County +: + +Kejimkujik National Park +, + +15 August 2001 +& +5 September 2001 + +, +2 specimens +, +B. Wright +, +NSMC + +. + + + + +Recorded +New York +and +Michigan +by Downie and Arnett (1996) who also list +Québec +as part this species’ range. + +Laplante +et al. +(1991) + +, however, which is a much more detailed compendium of the province’s fauna, does not include it nor does +Campbell (1991) +. Hence this specimen from +Nova Scotia +should be considered the first record of + + + +Table 1. +Maritime Provinces +Corylophidae +. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
NS
NewNorth ShoreCape BretonEast ShoreSouth ShoreBay of Fundy
CountyCUCOPIATINVICBRIGUHXSILUQUSHYADIANKIHANBPEI
+ +Corylophinae + +Parmulini +
+ +Clypastrea fasciata +(Say) + +1
1 + +Clypastrea fuscum +Harold + +1
1 + +Clypastrea lugubris +(LeConte) + +111
1 + +Clypastrea lunata +(LeConte) + +11
1 +Sericoderini + +Sericoderus lateralis +(Gyllenhal) + + +111
1 + +Orthoperinae + + +Orthoperus suturalis +LeConte + +1111111
1 + +Orthoperus scutellaris +LeConte + +111
1 + +Rypobiinae + +Rypobiini + +Rypobius marinus +LeConte + +1
1 +Gleosomatini + +Gloeosoma fusicornis +(Casey) + +1
1 + +Gloeosoma hesperus +(Casey) + +1
9Total022000202210401101131
+
+ + + +Adventive Palearctic species. + + + +this species in +Canada +. In +Nova Scotia +brushed from the bark of trees in a deciduous ( + +Acer +spp. + +, + +Quercus rubra + +L., and + +Betula +spp. + +) forest. + +
+
+
\ No newline at end of file diff --git a/data/38/3A/87/383A87F0FFBBFFBBFF2E79A1FC863557.xml b/data/38/3A/87/383A87F0FFBBFFBBFF2E79A1FC863557.xml new file mode 100644 index 00000000000..1a32f3b915a --- /dev/null +++ b/data/38/3A/87/383A87F0FFBBFFBBFF2E79A1FC863557.xml @@ -0,0 +1,133 @@ + + + +New Records of Corylophidae (Coleoptera) from the Maritime Provinces of Canada + + + +Author + +Majka, Christopher G. + + + +Author + +Cline, Andrew R. + +text + + +The Coleopterists Bulletin + + +2006 + +2006-06-30 + + +60 + + +2 + + +105 +111 + + + + +http://dx.doi.org/10.1649/864.1 + +journal article +10.1649/864.1 +1938-4394 + + + + + + + +Clypastrea fasciata +(Say) + + + + + + + +NEW BRUNSWICK +: +Kent County +: + +Kouchibouquac National Park +, + +21 September 1977 + +, +J.M. Campbell +, +CNC + +. + + + + +Recorded in +Canada +from +Ontario +, +Québec +, and +New Brunswick +Campbell (1991) +; in the +U.S.A. +in +Maine +(Dearborn and Donahue 1993), +New Hampshire +( +Chandler 2001 +), and from +Massachusetts +and +Michigan +south to +Florida +(Downie and Arnett 1996). The above record appears to be the source for the report of this species in +New Brunswick +in +Campbell (1991) +. In +Indiana +taken from beneath the bark of locust ( + +Robinia +sp. + +) and by sifting debris from a beech ( + +Fagus grandifolia +Ehrh. + +) stump ( +Blatchley 1910 +). In Europe +Bowestead (1999) +records various species of + +Clypastrea + +as associated with fungal and moldy situations under the bark of dead trees and in rotten wood. + + + + \ No newline at end of file diff --git a/data/38/3A/87/383A87F0FFBEFFBEFF157856FE563512.xml b/data/38/3A/87/383A87F0FFBEFFBEFF157856FE563512.xml new file mode 100644 index 00000000000..624d069a1dc --- /dev/null +++ b/data/38/3A/87/383A87F0FFBEFFBEFF157856FE563512.xml @@ -0,0 +1,242 @@ + + + +New Records of Corylophidae (Coleoptera) from the Maritime Provinces of Canada + + + +Author + +Majka, Christopher G. + + + +Author + +Cline, Andrew R. + +text + + +The Coleopterists Bulletin + + +2006 + +2006-06-30 + + +60 + + +2 + + +105 +111 + + + + +http://dx.doi.org/10.1649/864.1 + +journal article +10.1649/864.1 +1938-4394 + + + + + + + +Orthoperus scutellaris +LeConte + + + + + + + +NOVA SCOTIA +: +Digby County +: + +Brier Island +; +Pond Cove +, + +22 June 2003 +, +24 June 2003 +, +26 July 2003 +, +28 July 2003 +, +10 August 2004 +, +15 September 2004 + +, +J. Ogden +& +K. Goodwin +, +22 specimens +, +JOC + +; + + +Halifax County +: + +West Dover +, + +7 September 2003 + +, +C.G. Majka +, +CGMC + +; + +Sable Island +, 12–28 July, 2004, +Z. Lucas +, +NSMC + +. + + + + +Recorded in +Canada +from the +Northwest Territories +east to +Saskatchewan +( +Campbell 1991 +); in the +United States +from +New Hampshire +( +Chandler 2001 +), +Massachusetts +, +New York +, +Indiana +, and +California +(Downie and Arnett 1996). Newly recorded in Nova Scotia. A particularly noteworthy record is that from Sable Island on the continental shelf of Nova Scotia, +160 km +from the nearest point of mainland. The specimen was collected on an oily porpoise skull. + +Klimaszewski +et al. +(2006) + +discuss mechanisms of invertebrate colonization to this remote site including dispersal along island bridges from glacial refugia on George’s Bank, a mechanism that might be applicable to this species. In Europe some species of + +Orthoperus + +( +e.g., + +O. brunnipes +(Gyllenhal) + +and + +O. pilosiusculus +Jacquelin du Val + +) are regularly found in saline, coastal situations ( +Bowestead 1999 +) and all records of + +O. scutellaris + +in NS are from such habitats. + + + +Rypobiinae + + + + + +Rypobius marinus +LeConte + + + + + + +NEW BRUNSWICK +: +Albert County +: + +Mary’s Pt. +, + +12 August 2004 +& +21 August 2005 + +, sandy beach, +C.G. Majka +, +2 specimens +, +CGMC + +. + + +Recorded from the Atlantic seaboard of the +United States +from +New Hampshire +(Chandler 2000), and +Rhode Island +south to +Florida +: found on ocean beaches (Downie and Arnett 1996). Newly recorded from +Canada +. The specimen was collected under beach drift material at the top of the littoral zone below sand dunes on an ocean beach. The locale and the suite of sympatric beach-drift +Coleoptera +are discussed in detail in Majka and Ogden (2006) and Klimaszewski and Majka (submitted). +Pupedis (1997) +found it very abundant in a salt marsh in Connecticut. In Europe all species of + +Rypobius + +are associated with mould at the base of plants. One species, + +R. praetermissus +Bowestead + +, is tolerant of salinity and occurs mainly in salt marshes and at the edge of inland waters ( +Bowestead 1999 +). + + + + \ No newline at end of file diff --git a/data/38/3A/87/383A87F0FFBEFFBFFF157FDDFCFD308B.xml b/data/38/3A/87/383A87F0FFBEFFBFFF157FDDFCFD308B.xml new file mode 100644 index 00000000000..bc4ce976f6f --- /dev/null +++ b/data/38/3A/87/383A87F0FFBEFFBFFF157FDDFCFD308B.xml @@ -0,0 +1,107 @@ + + + +New Records of Corylophidae (Coleoptera) from the Maritime Provinces of Canada + + + +Author + +Majka, Christopher G. + + + +Author + +Cline, Andrew R. + +text + + +The Coleopterists Bulletin + + +2006 + +2006-06-30 + + +60 + + +2 + + +105 +111 + + + + +http://dx.doi.org/10.1649/864.1 + +journal article +10.1649/864.1 +1938-4394 + + + + + + + +Gloeosoma fusicornis +(Casey) + + + + + + + +NOVA SCOTIA +: +Colchester County +: + +Masstown +, + +7 September 2002 + +, marshy swamp, +8 specimens +, +C.G. Majka +, +CGMC + +. + + + + +In +Canada +recorded from +Ontario +and +Québec +( +Campbell 1991 +). +Sikes (2003) +reported it from Rhode Island. Specimens in +Nova Scotia +were collected by sweep-netting. + + +Newly recorded in +Nova Scotia +. Characteristically, records of species in this genus come from leaf litter or mould at the base of plants ( +Bowestead 1999 +). + + + + \ No newline at end of file diff --git a/data/38/3A/87/383A87F0FFBFFFBFFF2E7B5BFD55327F.xml b/data/38/3A/87/383A87F0FFBFFFBFFF2E7B5BFD55327F.xml new file mode 100644 index 00000000000..308fd2d31a9 --- /dev/null +++ b/data/38/3A/87/383A87F0FFBFFFBFFF2E7B5BFD55327F.xml @@ -0,0 +1,156 @@ + + + +New Records of Corylophidae (Coleoptera) from the Maritime Provinces of Canada + + + +Author + +Majka, Christopher G. + + + +Author + +Cline, Andrew R. + +text + + +The Coleopterists Bulletin + + +2006 + +2006-06-30 + + +60 + + +2 + + +105 +111 + + + + +http://dx.doi.org/10.1649/864.1 + +journal article +10.1649/864.1 +1938-4394 + + + + + + + +Gloeosoma hesperus +(Casey) + + + + + + + +NOVA SCOTIA +: +Queens County +: + +Kejimkujik National Park +, + +24 August–19 October 1994 + +, +3 specimens +, +B. Wright +, +NSMC + +; + +Kejimkujik National Park +, + +26 July 1995 + +, +B. Wright +, +NSMC + +; + +Kejimkujik National Park +, + +15 August 2001 + +, +B. Wright +, +NSMC + + +Kejimkujik National Park +, + +5 September 2001 + +, +2 specimens +, +B. Wright +, +NSMC + +. + + + + +In the +United States +reported from +Indiana +, +Iowa +, and +Nebraska +(Downie and Arnett 1996). Newly recorded in +Canada +. In NS brushed from the bark of trees in a deciduous forest ( + +Acer +spp. + +, + +Quercus rubra + +L., and + +Betula +spp. + +). In Indiana sifted from the debris of a beech ( + +Fagus grandifolia +Ehrh. + +) stump ( +Blatchley 1910 +). + + + + \ No newline at end of file diff --git a/data/38/3B/53/383B534898205DB78D066D14ED7ECE75.xml b/data/38/3B/53/383B534898205DB78D066D14ED7ECE75.xml new file mode 100644 index 00000000000..03db66b6b1d --- /dev/null +++ b/data/38/3B/53/383B534898205DB78D066D14ED7ECE75.xml @@ -0,0 +1,710 @@ + + + +Can you find me? A new sponge-like nudibranch from the genus Jorunna Bergh, 1876 (Mollusca, Gastropoda, Discodorididae) + + + +Author + +Tibirica, Yara +https://orcid.org/0000-0003-3955-8186 +Departamento de Biologia, Facultad de Ciencias del Mar y Ambientales, Campus de Excelencia Internacional del Mar (CEI · MAR), Universidad de Cadiz, Av. Republica Saharaui, s / n, 11510 Puerto Real (Cadiz), Spain +yara.tibirica@gm.uca.es + + + +Author + +Stroemvoll, Jenny +Instituto Universitario de Investigacio ́ n Marina (INMAR), Campus de Excelencia Internacional del Mar (CEI · MAR), Universidad de Ca ́ diz, Av. Repu ́ blica Saharaui, s / n, 11510 Puerto Real (Ca ́ diz), Spain + + + +Author + +Cervera, Juan Lucas +https://orcid.org/0000-0002-8337-2867 +Departamento de Biologia, Facultad de Ciencias del Mar y Ambientales, Campus de Excelencia Internacional del Mar (CEI · MAR), Universidad de Cadiz, Av. Republica Saharaui, s / n, 11510 Puerto Real (Cadiz), Spain + +text + + +Zoosystematics and Evolution + + +2023 + +2023-01-13 + + +99 + + +1 + + +63 +75 + + + + +http://dx.doi.org/10.3897/zse.99.95222 + +journal article +http://dx.doi.org/10.3897/zse.99.95222 +1860-0743-1-63 +7D011FEE8B7D48D5968A129CB317B9B2 +F13322B4EA435C6CAB5B8FCE42760563 + + + + + +Jorunna liviae +Tibirica +, +Stroemvoll +& Cervera + +sp. nov. + + + + +Jorunna +sp.: +Stroemvoll +, J. & Jones, G. (2019): pg.49. + + + +Material examined. + + + +Holotype + +: MNCN15.05/200187 (dissected and sequenced), +12.04.2022 +, +Doodles +, +Ponta do Ouro +, +Mozambique +, depth + +15 m + +, length +20 mm +. + + + + + +Paratypes + +: MNCN15.05/200188 (dissected and sequenced), +12.04.2022 +, +Doodles +, +Ponta do Ouro +, +Mozambique +, depth + +17 m + +, length +11 mm +. MNCN15.05/94693 (sequenced and tomography), +12.04.2022 +, +Doodles +, +Ponta do Ouro +, +Mozambique +, depth + +15 m + +, length +20 mm +., size +5 mm +. MNCN15.05/200189 (dissected and sequenced), +14.04.2022 +, +Doodles +, +Ponta do Ouro +, +Mozambique +, depth + +18 m + +, length +13 mm +. MHNM.MOL.2022.0002, (2 specs.), +23.06.2022 +, +Steps Reef +, +Ponta do Ouro +, +Mozambique +, depth + +16 m + +, length +30 mm +(both) + +. + + + +Type locality. + +Ponta do Ouro, Mozambique ( +26°51'26"S +, +32°53'4"E +). + + + +Habitat. +Specimens were collected on submerged subtropical compressed sandstone reefs in Ponta do Ouro, Mozambique. + + +Diagnosis. +Body elongate-ovulated. Dorsum pale gray to pink, covered on highly dense caryphyllidia; rhinophores short, with up to nine lamellae, ending in a knob apex; six to nine bipinnate branchial leaves encircling the anal pore. Radula with five to seven very thin pectinated outermost teeth bearing long bundled fibrous denticles. Labial cuticle smooth. Copulatory spine with bifid apex. + + +Etymology. + +This species is dedicated to Livia +Renee +Cornelius, daughter of the second author of this paper. + + + +Description. + +External morphology +(Figs +1 +, +2 +). Length varied from 11 to 30mm. Body elongate-ovulated, with gritty texture (Fig. +1A +). Mantle covered on highly dense caryophyllid, evenly distributed on the dorsum (Fig. +2A +). Caryophyllidia elongated, formed by five to eight spicules, projecting over tip, forming a crown of approximately 140 +µm +on the dorsum, taller on the margin of gill sheath (≈ 280 +µm +). Rhinophoral and branchial sheaths low, margin covered by caryophyllidia (Fig. +1D +). Rhinophores short, retractable, with six to eight diagonal lamellae with a knob protruding apex (Fig. +1E +). Gill with six to nine retractile, bipinnate branchial leaves, held vertically and forming a closed circle around the anal pore (Fig. +1F +). Foot narrower than mantle, bilabiate anteriorly, upper lip bifurcate at center (Fig. +1B +). Side of the foot covered by spicules (≈ 60 +µm +), spicules absent on foot sole (Figs +1B, C +, +2B, C +). Feet do not project beyond mantle in natural crawling position. Oral tentacles small and conical. Dorsum color pale pink to gray. Some specimens covered by pinkish-brown minute dots forming spots distributed on the notum. Gill and rhinophores translucent pinkish-white. Oral tentacle white. Upper lip translucent white with brownish dots. Foot pinkish-white. + + + +Figure 1. + +Jorunna liviae + +sp. nov. (MNCN15.05/200187) external morphology. +A. +Dorsal view; +B. +Ventral view; +C. +SEM photography of dorsal caryophyllids; +D. +Rhinophores sheath details; +E. +Rhinophore; +F. +Gill branches. + + + + +Figure 2. +Microcomputed tomography (µCT) of + +J. liviae + +sp. nov. (MNCN15.05/94693). +A. +Exterior view: dorsal (top) and anterior (bottom); +B. +Internal arrangement of the spicules: dorsal (top) and ventral (bottom); +C. +General internal arrangement of spicules: green = top right; blue = middle right; red = bottom right. + + + + +Internal morphology +. + +(Figs +3 +, +4 +) The visceral mass is enveloped by a translucent-white tissue covered by brownish dots. Eye spots are visible by transparency. + + + +Figure 3. +SEM photographs of + +Jorunna liviae + +sp. nov. +A. +labial cuticle (MNCN15.05/200188); +B. +entire view of the radula; +C. +Half-row of posterior part of the radula; +D. +Outermost teeth; +E. +Detail of the outermost teeth; +F. +Copulatory spine. + + + + +Figure 4. + +Jorunna liviae + +sp. nov. internal anatomy. +A. +Oral mass; +mo +- mouth; rm - retractor muscles; +ob +- oral bulb; +oe +- oesophagus; +ot +- oral tube; +rs +- radular sac; +sg +- salivary gland; +B. +Central system (blood gland removed); +cg +- cerebral ganglia; cp - pedal commissure; +ey +- eye; +gp +- pedal ganglia; +pl +- pleural ganglia; +rg +- rhinophoral ganglia; +C. +Reproductive system; +ag +- accessory gland; +amp +- ampulla; +bc +- bursa copulatrix; +cs +- copulatory spine; +dd +- deferent duct; +pr +- prostate; +sr +- seminal receptacle; +ud +- uterine duct; +vag +- vagina. + + + + +Digestive system. + +Smooth labial cuticle (Fig. +3A +). Oral tube long, about twice the size of oral bulb, with a pair of retractor muscles (Fig. +4A +). Buccal bulb ovate, short, radular sac small and ovate, protruding ventrally, with a pair of strong retractor muscles (Fig. +4A +). + + +Radular formula difficult to determinate as outermost teeth are very thin and overlapping each other (Fig. +3B +). Approximate radular formula is: 24 +x +5-7.22.0.22.5-7 for the 13 mm specimen MNCN15.05/200189 and 38 +x +6-7.26.0.26.6-7 for the 20 mm specimen MNCN15.05/200187. Rachidian tooth absent. Innermost and lateral teeth are single cusped, hamate, lacking denticles (Fig. +3C +). Lateral teeth gradually increase in size from the inner teeth (≈ 25 +µm +) toward the external margin (outermost teeth ≈ 100 +µm +). Five to seven outermost teeth highly differentiated, very thin, pectinate, bearing 5 to 9 long bundled fibrous denticles (Fig. +3D, E +). + +Oesophagus passing through nerve ring, where it folds. Pair of salivary glands, relatively short, uniform, near the base of oesophagus (4A). Oesophagus connects to oval stomach. Intestine about half of oesophagus diameter. Caecum locate ventrally to stomach. Digestive gland cone-shaped, occupying approximately 30% of visceral mass. Anus opening at the center of gill circle. + + +Central nervous system. + +Central nervous system partially covered by blood gland. This is divided into two parts, anterior part about half the size of posterior part. Cerebral ganglia about half the size of pleural ganglia. Cerebral ganglia and pleural ganglia fused. Pedal ganglia ventrally located connected by a simple pedal commissure. Buccal ganglia short, ventrally located. Rhinophoral ganglia bulb-shaped, about 30% the size of cerebral ganglia. Eyes connected to cerebral gland by short rhinophoral nerve (Fig. +4B +). + + + +Reproductive system. + +Hermaphroditic duct leading to an ampulla long and convoluted, located between female gland and accessory gland. Ampulla branching into short oviduct and prostate. Flattened and ovulated prostate narrowing into a thin deferent duct, expanding into ejaculatory portion. Penis unarmed. Accessory gland size and shape varied according to the specimen, from pear-shaped and similar size to the female gland MNCN15.05/200187 to elongated and half of the size MNCN15.05/200189; in all specimens it narrows into a very thin, highly convoluted tube. Copulatory spine in accessory gland of approximately 1.25 mm (Fig. +3F +). Vagina with similar length and width than deferent duct, leading to an oval bursa copulatrix. Thin duct near the vagina leads to oval seminal receptacle, about 2/3 of the size of the bursa copulatrix, which connects to a large female gland by a short uterine duct (Fig. +4C +). + + + +Natural history. + +This species has only been seen associated with the sponge + +A. brevispiculifera + +, on which the species is very cryptic (Fig. +5A, B +). They are usually found at the base of the sponge branches but they have also been seen on other parts. When removed from the host sponge, the + +Jorunna liviae + +sp. nov. stretches the body curling the mantle toward the middle of the foot, similar to what +Miller (1996) +observed for + +J. ramicola + +. Perhaps this behavior aims to protect the sole of the foot which lacks caryophylliid. The white egg mass is also found on the same sponge and forms a close spiral ribbon of approximately five coils (Fig. +5F +). A likely undescribed species of nudibranch egg-eater + +Favorinus + +sp. has been seen feeding on the + +J. liviae + +sp. nov. egg mass (Fig. +5C, D +). Curiously, most of the time the egg ribbons are found on the tip of the sponge. Perhaps this strategy provides some protection against encrusting organisms due the higher water flux in this part of the sponge. Mating has been observed through July between specimens of different sizes and tonalities (Fig. +5E +). + +Jorunna liviae + +sp. nov. seems to prefer sandy reefs with predominantly hydroids, soft coral and sponges. In Southern Mozambique, the flatter sand reefs have a higher density of sponges than the reefs with predominantly hard coral. + + + +Figure 5. + +Jorunna liviae + +sp. nov. +in situ +. +A. +Hosting sponge + +Amphimedon brevispiculifera + +(Dendy, 1905); +B. + +Jorunna liviae + +sp. nov. resting on sponge; +C. + +Jorunna liviae + +sp. nov. near its egg mass, and + +Favorinus + +sp. feeding on it; +D. +Close-up of + +Favorinus + +sp.; +E. + +Jorunna liviae + +sp. nov. mating; +F. +Details of + +Jorunna liviae + +sp. nov. egg mass. + + + + +Molecular study and phylogeny. + +We successfully amplified the gene COI and H3 of four + +Jorunna liviae + +sp. nov. specimens. The phylogenetic trees constructed by BI and ML analyses of single gene datasets (Suppl. material 1) were not conflictive but differed in the ability to resolve phylogenetic relationships. The single gene H3 analysis retrieved the lowest resolution and the concatenate dataset the highest. Nevertheless, all + +Jorunna + +species were recovered with more than 50% support in all analysis. In general, the BI analysis better solved the relationship between species, while the ML analysis appears to reflect populational structure. Therefore, the results discussed below are based on the concatenated analysis (Fig. +6 +), except when stated otherwise. + + + +Figure 6. +Bayesian inference tree based on the concatenate sequence dataset (COI+H3) collapsed (PP<0.5). Numbers at the top of nodes indicate Bayesian Posterior probability (PP) and on the bottom bootstrap support from the maximum likelihood analysis (BS). Colored bars on the right represent the results of the species delimitation analyses on the + +Jorunna + +spp., from left to right: ASAP on COI dataset, PTP on COI dataset, bPTP on COI+H3 dataset. + + + +The family +Discodorididae +formed a large polytomy. The genus + +Jorunna + +was divided in two paraphyletic clades, one containing all specimens of + +J. funebris + +(PP = 1; BS = 94) and another clade with the remaining + +Jorunna + +species (PP = 0.99; BS = 74). + + +The COI inter-specific variation (uncorrected +p +-distance) within the genus varied from 9.08% between + +J. tomentosa + +lineage B (LB) and + +J. artsdatabankia + +to up 16.92% between + +J. funebris + +and + +J. tomentosa + +lineage A (LA) (Table +1 +). The COI intra-specific variation of + +Jorunna liviae + +sp. nov. ranged from 0.16% to 1.08%. The closest species to + +Jorunna liviae + +sp. nov. was + +J. tomentosa + +lineage B with a minimum +p +-distance of 13.06%. ASAP retrieved 10 partitions, in both analysis (COI and concatenate) the partitions with higher score (asap-score 1.50-3) + +Jorunna liviae + +sp. nov. was retrieved as a distinct taxonomic unit. Curiously, + +J. funebris + +were retrieved as a species complex in all possible partitions. + + + +Table 1. +COI inter- and intraspecific uncorrected +p +-distances. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
- + +Jorunna artsdatabankia + + + +Jorunna tomentosa + +LA + + +Jorunna tomentosa + +LB + + +Jorunna liviae + +sp. nov. + + +Jorunna onubensis + +Intra-specific
+ +Jorunna artsdatabankia + +-----0-0.15%
+ +Jorunna tomentosa + +LA +10.30----0.15-0.68%
+ +Jorunna tomentosa + +LB +9.083.65---0.15-0.92%
+ + +Jorunna liviae + +sp. nov. + +14.2914.7413.06--0.16-1.08%
+ +Jorunna onubensis + +12.6110.7410.4512.31-N/A
+ +Jorunna funebris + +16.9217.7817.7816.9216.920.46-14.18%
+
+
+
+
\ No newline at end of file diff --git a/data/38/3B/8A/383B8AD6B93D9ACBBCCB1601BE9E2167.xml b/data/38/3B/8A/383B8AD6B93D9ACBBCCB1601BE9E2167.xml new file mode 100644 index 00000000000..9d472253a54 --- /dev/null +++ b/data/38/3B/8A/383B8AD6B93D9ACBBCCB1601BE9E2167.xml @@ -0,0 +1,76 @@ + + + +Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea + + + +Author + +Dale-Skey, Natalie + + + +Author + +Askew, Richard R. + + + +Author + +Noyes, John S. + + + +Author + +Livermore, Laurence + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8013 +8013 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8013 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8013 +1314-2828--8013 + + + + +Metaphycus melanostomatus (Timberlake, 1916) + + + + +Aphycus melanostomatus +Timberlake, 1916 + + + +Distribution +England, Scotland, Wales, Ireland + + + \ No newline at end of file diff --git a/data/38/3B/99/383B99666F8F14C56E43CE848DFABC36.xml b/data/38/3B/99/383B99666F8F14C56E43CE848DFABC36.xml new file mode 100644 index 00000000000..23bfea5d8ce --- /dev/null +++ b/data/38/3B/99/383B99666F8F14C56E43CE848DFABC36.xml @@ -0,0 +1,131 @@ + + + +The beetle fauna (Insecta, Coleoptera) of the Rawdhat Khorim National Park, Central Saudi Arabia + + + +Author + +Abdel-Dayem, Mahmoud S. +https://orcid.org/0000-0002-6276-1740 +King Saud University Museum of Arthropods (KSMA), Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, P. O. Box 2460 Riyadh 11451, Saudi Arabia +mseleem@ksu.edu.sa + + + +Author + +Fad, Hassan H. +Entomology Department, Faculty of Science, Ain Shams University, Cairo, Egypt + + + +Author + +El-Torkey, Ashraf M. +Plant Protection Research Institute, Agriculture Research Center, Giza, Egypt + + + +Author + +Elgharbawy, Ali A. +King Saud University Museum of Arthropods (KSMA), Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, P. O. Box 2460 Riyadh 11451, Saudi Arabia & Zoology Department, Faculty of Science, Al Azhar University, Nasr City, Cairo, Egypt + + + +Author + +Aldryhim, Yousif N. +King Saud University Museum of Arthropods (KSMA), Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, P. O. Box 2460 Riyadh 11451, Saudi Arabia + + + +Author + +Kondratieff, Boris C. +Department of Bioagricultural Sciences and Pest Management, Colorado State University, Campus Delivery 1177, Fort Collins, Colorado, U. S. A. 80523 + + + +Author + +Ansi, Amin N. Al +King Saud University Museum of Arthropods (KSMA), Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, P. O. Box 2460 Riyadh 11451, Saudi Arabia + + + +Author + +Aldhafer, Hathal M. +King Saud University Museum of Arthropods (KSMA), Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, P. O. Box 2460 Riyadh 11451, Saudi Arabia + +text + + +ZooKeys + + +2017 + +2017-02-07 + + +653 + + +1 +78 + + + + +http://dx.doi.org/10.3897/zookeys.653.10252 + +journal article +http://dx.doi.org/10.3897/zookeys.653.10252 +1313-2970-653-1 +8ECC0674017A48588BE8DDD05C0D7CF6 +FFE87C63852C5772725FBE55FF95902D +269679 + + + + +Typhaea stercorea (Linnaeus, 1758) + + + +World distribution. + +Africa +: GM, MR, ZA. +Asia +: AE, AF, AZ, BT, CN, CY, EG (Sinai), IL, IQ, IR, JO, JP, KG, KR, KZ, MN, NP, PK, RU, SA, SY, TJ, TM, TR, UZ, YE. +Europe +: AD, AL, AM, AT, BA, BE, BG, BY, CH, CZ, DE, DK, EE, ES, FI, FO, FR, GB, GE, GR, HR, HU, IE, IS, IT, LI, LT, LU, LV, MD, MK, MT, NL, NO, PL, PT, RO, RS, RU, SE, SI, SK, UA. +North Africa +: DZ, EG, ES (Canary Islands), LY, MA, PT (Madeira Archipelago), TN. +South America +: CL. + + + +General distribution. +COS. + + +Local distribution. + +BA ( +El-Hawagry et al. 2013 +). + + + +Collecting month and method. +Very rare species. The adults were collected by LT during V. + + + \ No newline at end of file diff --git a/data/38/3B/D7/383BD70A8E038EA7AF018D77CD52F8EE.xml b/data/38/3B/D7/383BD70A8E038EA7AF018D77CD52F8EE.xml new file mode 100644 index 00000000000..f936624b69a --- /dev/null +++ b/data/38/3B/D7/383BD70A8E038EA7AF018D77CD52F8EE.xml @@ -0,0 +1,76 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828--9042 + + + + +Adelognathus brevicornis Holmgren, 1857 + + + + +limbatus +Thomson, 1888 + + +montivagator +Aubert, 1976 + + + +Distribution +England, Scotland, Ireland + + +Notes + +The +chrysopygus +(Grav.) referred to by +Fitton et al. (1982) +actually refers to +punctulatus +Thoms.; +chrysopygus +is the correct name for the species referred to as granulatus Perkins by +Fitton et al. (1982) +( +Kasparyan 1986 +). Some distribution data from +Bennett et al. (2002) +. + + + + \ No newline at end of file diff --git a/data/38/3B/E2/383BE237A67EFFEB6CA2C6E1537629F2.xml b/data/38/3B/E2/383BE237A67EFFEB6CA2C6E1537629F2.xml new file mode 100644 index 00000000000..ddebe5db4df --- /dev/null +++ b/data/38/3B/E2/383BE237A67EFFEB6CA2C6E1537629F2.xml @@ -0,0 +1,479 @@ + + + +A new Hyalella species (Crustacea: Amphipoda: Hyalellidae) from South American Highlands (Argentina) with comments on its cuticular ultrastructure + + + +Author + +Verónica, Isa Miranda Águeda +0000-0002-3300-7490 +Instituto de Invertebrados, Fund. M. Lillo, Miguel Lillo 251, T 4000 JFE-San Miguel de Tucumán, Argentina. & CONICET fellowship. aguedaveronica 9 @ gmail. com; https: // orcid. org / 0000 - 0002 - 3300 - 7490 +aguedaveronica9@gmail.com + + + +Author + +Alejandra, Peralta Marcela +Instituto de Invertebrados, Fund. M. Lillo, Miguel Lillo 251, T 4000 JFE-San Miguel de Tucumán, Argentina. + +text + + +Zootaxa + + +2022 + +2022-03-03 + + +5105 + + +2 + + +202 +218 + + + +journal article +20380 +10.11646/zootaxa.5105.2.2 +353cfdc2-dda2-46fc-b613-18d519536ec0 +1175-5326 +6332543 +8DADBF00-2FEA-4B0F-8C24-06A5897DCD68 + + + + + + + +Hyalella fatimae + +n. sp. + + + + + + +( +Figs. 1–7 +) + + + + + + +Type +locality. +Argentina + +, +Salta Province +, +Los Andes Department +: +24°13’6.41’’S +66°28’24.09’’W +( +Fig. 1 +), + +4458 m +a.s.l. + +, peatbog near to Chorrillos + +. + + +Type specimens: + +Holotype +male, body length +8.10 mm +( +FML-CRUST 01273 +) + +. + +Paratypes +: +one female +(ovigerous), body length +6.92 mm +( +FML-CRUST 01274 +) + +; + +two males +, body length 5.8 and +7.57 mm +( +FML-CRUST 01275 +). +All +collected at type locality ( +Fig. 1 +), + +18-XII-2013 + +; +Col. J. Rodríguez. + + + +Additional material: + + +Argentina +; + +3 males +, +7 females +Argentina +; +Salta Province +, peatbogs vega + +Abra +de Chorrillos + +, left branch (VC1C); +24°11’38’’S +66°32’15’’W +( +Fig. 1 +). + +4358 m +a.s.l. + +, + +17-XII-2013 + +; +Col. J. Rodríguez +( +FML- +CRUST 01277 +). + + +One +female, +Argentina +, +Salta Province +, +Los Andes Department +: +24°13’6.41’’S +66°28’24.09’’W +, + +4458 m +a.s.l. + +, peatbog near to +Chorrillos +, + +18-XII-2013 + +; +Col. J. Rodríguez +( +FML-CRUST 01276 +, SEM preparations) + +. + + + + +Diagnosis. +Antenna 1 shorter, barely longer than head. Inner plate of maxilla 1 reaching base of palp, with two short and robust pappose setae. Inner plate of maxilla 2 with one robust papposerrate seta. Propodus of male gnathopod 1 hatchet-shaped, with nine serrate setae on inner face, palm angle with three cuspidate setae with accessory seta (one longer external, two shorter, internal). Epimeral plate I rounded, II and III posterodistally slightly acuminate. + + + + +Etymology. +The species epithet “ fatimae “ honors the limnologist Fátima Romero (Fundación Miguel Lillo- +Tucumán +, +Argentina +) for her contributions to the study of freshwater macroinvertebrates in +Argentina +. + + +Habitat. +Freshwater, epigean. + + + + +FIGURE 1 +. Map showing distribution of + +Hyalella kochi + +, + +H. fossamancinii +, +H. puna + +and + +H. fatimae + + +n. sp +. + +in northwestern Argentina within a biogeographic scheme. + + + + + +Description of +Holotype +male. + +Size, +8.10 mm +. Head smaller than first two thoracic segments combined. Eyes pigmented, large, subrounded. Body surface smooth. Epimeral plate I rounded, different from plates II and III, which are posterodistally slightly acuminate ( +Fig. 4A +). Pereiopodal coxae I to III subequal in shape, slightly overlapping. Acumination in coxae absent. Coxa III narrower than IV. Coxa IV deeper than wide, excavated posteriorly. Posterior lobe of coxa V deeper than anterior lobe. Anterior lobe of coxa VI small ( +Figs 7A–D +). + + +Antenna 1 ( +Fig. 4B +) much shorter than antenna 2 but longer than peduncle of latter; peduncle shorter than head, first segment ⅓ longer than second one, third segment slightly shorter than second; all segments of peduncle with group of simple setae; in addition, second segment with medial plumose seta. Flagellum of eight articles, all with groups of simple setae, additionally 1–2 aesthetascs per article arranged distally between articles 5–7, distal article with group of four long setae and one small simple seta. + + +Antenna 2 ( +Fig. 4C +) less than half of body length, with peduncle slightly longer than head, article 4 shorter than article 5; articles 3–5 with groups of simple setae, and 1–2 plumose setae, article 5 with other simple medial setae. Flagellum with 10 articles, distally with group of simple setae, and some articles with plumose setae. + + +Labrum ( +Fig. 4D +) ventral margin truncate, covered by short distal setules. + + +Mandibles basic amphipodan +type +(sensu +Watling 1993 +); each with well-developed large, cylindrical, triturative molar. Left mandible ( +Fig. 4F +) incisor 6-denticulate (three short, three long); lacinia 3-denticulate; setal row with five pappose setae. Right mandible ( +Fig. 4E +) incisor 6-denticulate (three very short, three long); lacinia complex, setal row with two pappose setae. + + +Lower lip ( +Fig. 5A +) outer lobes rounded with distal and internal setules, mandibular projection of outer lobes round. Inner lobes wanting + + + +FIGURE 2. + +Hyalella fatimae + + +n. sp +. + +, male paratype, habitus (photograph). + + + +Maxilla 1 ( +Fig. 5B +) palp unsegmented, longer than wide, reaching more than half the distance between base of palp and base of setae on outer plate, setulose and with strong papposerrate seta distally; nine serrate long distal setae on outer plate; inner plate slender, shorter than outer one, bearing two apical papposerrate setae; both plates with setules and denticles on outer face. + + +Maxilla 2 ( +Fig. 5C +) plates subequal in length. Inner plate with one strong, long papposerrate seta proximally on inner margin. Both plates sparsely setulose, with apex wearing serrulate, simple, pappose and serrate setae as figured. + + +Maxilliped ( +Fig. 5D +) inner plate apically rounded, longer than wide, with three strong cuspidate setae, apex and margins with setules, pappose and simple setae; outer plate with apical pappose setae continuous with a row of simple setae that cover most of medial margin; outer distal face of both plates with 1–2 short setae; palp longer than outer plate, 4-segmented, second segment longer than wide; inner margins of segments 2 and 3 with several long simple setae; outer distal face of segments 1 and 2 with 1–3 setae; inner distal margin of segment 3 with seven serrate setae; segment 4 unguiform, shorter than segment 3, with thin apical seta shorter than distal nail. + + +Coxal gills on gnathopod 2 ( +Fig. 6B +) to pereiopod 6 ( +Figs. 7A–C +), sac-like. Sternal gills tubular on pereionites II–VII. + + +Gnathopod 1 ( +Fig. 6A +) subchelate. Coxal plate margin with small simple setae. Basis, ischium and merus with serrate setae on posterior margin. Carpus longer than wide, with strong, wide concave posterior lobe, border pectinate and with several serrate setae. Propodus length less than two times maximum width, hatchet-shaped, anterodistal border with group of thin simple setae, inner face with nine serrate setae; denticles of +type +T1 on postero-distal border; palm slope slightly transverse, margin slightly convex covered with simple setae; palm angle with three cuspidate setae with accessory seta (one longer, external). Dactylus claw-like, inner margin with denticles and three endal setae, outer margin with one thin plumose seta dorsally. Palmar Index (sensu +Ruffo 1973 +) = 0.44. + + + +FIGURE 3. + +Hyalella fatimae + + +n. sp +. + +, male paratype, habitus (drawing) + + + +Gnathopod 2 ( +Fig. 6B +) subchelate. Basis approximately 2x longer than wide; posterior margin with five long serrate setae. Basis, ischium and merus each with group of setae on postero-distal border. Posterior lobe of carpus elongated, border pectinate with some serrate setae. Propodus ovate, with scales on postero-distal margin; palm margin slightly longer than posterior margin, with slope slightly oblique, straight and regular with several strong short and medium-length setae; antero-distal border with cluster of thin simple setae; palm angle with two cuspidate setae with an accessory seta. Dactylus claw-like with several endal setae and comb-scales, congruent with palm, with one thin plumose seta dorsally. Palmar Index (sensu +Ruffo 1973 +) = 0.47. + + +Pereiopods 3–4 ( +Figs. 7A, B +) similar in size and shape. Coxal plate of pereiopod 3 longer than wide; coxa of pereiopod 4 excavated posteriorly, deeper than wide; both coxal plates with margins bordered with thin simple setae; posterior margin of basis, ischium, merus, carpus and propodus with simple or cuspidate setae; anterior margin of merus, carpus and propodus with cluster of distal setae; dactylus less than half length of propodus, with one plumose seta. + + +Pereiopods 5–7 ( +Figs. 7C–E +) pereiopod 5 distinctly shorter than 6 and 7, which are subequal in length. Coxal plate of pereiopod 5: wider than long, posterior lobe deeper than anterior; coxa of pereiopod 6: as long as wide, anterior lobe much reduced; coxa of pereiopod 7: wider than long; all coxal plates with thin simple setae on margin. Posterior margin of basis of pereiopods 5–7 expanded (more so in 5 and 7 than in 6) and finely serrate. Anterior margins of basis, merus, carpus and propodus with marginal clusters of 2–6 cuspidate setae; dactylus 5 less than half length of propodus, dactylus 6–7 not reaching half length of propodus, all with a plumose seta. + + +Pleopods ( +Fig. 8A +) all similar, peduncle shorter than rami, biramous; rami multi-annulated and bearing long plumose setae. + + +Uropod 1 ( +Fig. 8B +) peduncle 1.4 times longer than rami, with three proximal cuspidate setae aligned in a longitudinal row and two other distal cuspidate setae; rami subequal in length; outer ramus with two dorsal and four distal cuspidate setae; inner ramus with two dorsal and five distal cuspidate setae (one of them slender); modified curved seta on inner side of inner ramus wanting. + + + +FIGURE 4. + +Hyalella fatimae + + +n. sp +. + +, male holotype. +A +epimeral plates +B +antenna 1, arrow indicates detail of the two distal articles +C +antenna 2 +D +labrum +E +right mandible, arrow indicates detail of incisor +F +left mandible. Scale bars: 0. 1 mm. + + + + +FIGURE 5. + +Hyalella fatimae + + +n. sp +. + +, male holotype. +A +lower lip +B +maxilla 1 +C +maxilla 2 +D +left maxilliped. + + + +Uropod 2 ( +Fig. 8C +) shorter than uropod 1; peduncle subequal to rami, with four cuspidate setae; rami subequal with two proximo-dorsal cuspidate setae; inner ramus of left uropod 2 with four cuspidate setae at the distal end, one of them longer than rest; apex of inner ramus of right uropod 2 with five cuspidate setae; apex of outer ramus with four cuspidate setae (one of them shorter than rest). + + +Uropod 3 ( +Fig. 8D +) much shorter than peduncle of uropod 2; peduncle slightly longer than wide, wider than ramus, with two strong cuspidate distal setae and two other thin simple marginal setae; outer ramus unsegmented, shorter than peduncle, basal width near 1.6 times tip of ramus, apex with three simple setae, and one cuspidate shorter seta. + + +Telson ( +Figs. 8E, F +) wider than long, entire, bearing two widely apart simple setae, symmetrically distributed on distal margin, and with two or three short plumose setae at each side laterally to the simple ones. + + +Females. Measurements: +Body length ranging from +3.28 to 7.5 mm +; mean body size: +4.59 mm +(8 individuals). Habitus similar to male except for the following characters: Antenna 1 flagellum with 5–7 articles. Antenna 2 flagellum with 6–10 articles. Gnathopods 1 and 2 similar to each other in size and shape. Gnathopod 1, inner face of propodus with eight serrate setae ( +Fig. 6C +). Gnathopod 2, inner face of propodus with five serrate setae ( +Fig. 6D +); gnathopod 2 differs from that of the male in shape and smaller propodus. Oostegites subtriangular, with curled setae on the margins ( +Fig. 6D +). + + +Variability in males: +Measurements: body length ranging from +5.8 to 9.5 mm +; mean body size: +7.8 mm +(6 individuals). Some variations were observed in the setae of gnathopod 1 propodus, setae of uropods 2–3, and number of flagellum articles of antennae. Gnathopod 1: some males with seven serrate setae on inner face of propodus (instead of nine). Uropods: in +one adult +male, peduncle of right uropod 3 with four connate setae (left peduncle with three); another adult male, uropod 3 peduncle with three connate setae, two long and one short, ramus with one simple seta (instead of three). In +one adult +male, uropod 2 peduncle with four marginal cuspidate setae (two in +holotype +). Number of articles in antennal flagellum increases with size of the individual, in largest male ( +9.5 mm +) A1 with 10–11 articles, A2 with 13–14 articles; in smallest male ( +5.8 mm +) A1 had only 8 articles and A2 only 10 articles. + + + + \ No newline at end of file diff --git a/data/38/3C/62/383C626781425FB4B169758569BF4226.xml b/data/38/3C/62/383C626781425FB4B169758569BF4226.xml new file mode 100644 index 00000000000..43a8d1c4509 --- /dev/null +++ b/data/38/3C/62/383C626781425FB4B169758569BF4226.xml @@ -0,0 +1,162 @@ + + + +A review of Gryllidae (Grylloidea) with the description of one new species and four new distribution records from the Sindh Province, Pakistan + + + +Author + +Sultana, Riffat +Department of Zoology, University of Sindh, Jamshoro, Sindh, Pakistan +riffat.sultana@usindh.edu.pk + + + +Author + +Sanam, Surriya +Department of Zoology, University of Sindh, Jamshoro, Sindh, Pakistan + + + +Author + +Kumar, Santosh +https://orcid.org/0000-0002-4748-4087 +Department of Zoology, Cholistan University of Veterinary and Animal Sciences, Bahawalpur, Punjab, Pakistan + + + +Author + +R, Sheik Mohammad Shamsudeen +Department of Zoology, Sir Syed college, Kannur University, Kerala, India + + + +Author + +Soomro, Fakhra +Department of Zoology, Shah Abdul Latif University, Khairpur, Sindh, Pakistan + +text + + +ZooKeys + + +2021 + +2021-12-15 + + +1078 + + +1 +33 + + + + +http://dx.doi.org/10.3897/zookeys.1078.69850 + +journal article +http://dx.doi.org/10.3897/zookeys.1078.69850 +1313-2970-1078-1 +573D406716A24E20859D354DFAF83B4D +7750940F8C815500968DBCC909A8E406 + + + + +Callogryllus ovilongus Saeed & Yousuf, 2000 + + + + +Figures 1 +, 2 +, 3 +, 4 +, 5 +, 6 +, 7 +, 8 +, 9 +, 10 +, 11 + + + +Material examined. + + +Pakistan +, + +Sindh Prov. + +• +4♀ +; +Riffat +, +Surriya +; +16 Sep. 2020 +; Nagarparkar +24.3572°N +, +70.7555°E + +. + + + +Description. + +Medium size. Colouration yellow (Fig. +1Q +). Head short, narrow, very neat. Eyes rounded, moderately projecting; ocelli small (Fig. +3F +). Pronotum 1.5 +x +as wide as long, slightly concave at anterior margin, straight at posterior margin; one side rather strongly convex (Fig. +5G +). Elytra yellow, reduced (Fig. +10D +). No wings. Legs light yellow, hind femora thick at base and slightly narrow at posterior, armed with six internal spines. Hind tibiae small, narrow, and straight. Abdomen dark yellowish above, pubescent and pale yellow beneath. Ovipositor rather long, very slender with extremely narrow, acute apical valves (Fig. +1Q +). + + +Female +: LH 3.85 (mm), LP 3.5 (mm), LT 5.2 (mm), LF 4.1 (mm), LO 15 (mm), TBL 16 (mm). + + + +Ecology. +During the present study, females of this species are reported from Nagarparkar, Desert Thar, from xerophytic plants which were surrounded by sagebrush and saltbush trees. + + +Global distribution. + +China, India, Bangladesh, Nepal, Pakistan ( +Cigliano et al. 2020 +). + + + +Remarks. + +This species was erected by +Saeed (2000) +from Peshawar, KPK based on a single female specimen; subsequently +Malik et al. (2013) +reported its male from the Hyderabad -Sindh. We have a single female from the rocky area of Nagarparkar and confirm its presence in the desert area. + + + + \ No newline at end of file diff --git a/data/38/3D/13/383D13A64823382BAB67404BBA514EEF.xml b/data/38/3D/13/383D13A64823382BAB67404BBA514EEF.xml new file mode 100644 index 00000000000..ce5f4d464fd --- /dev/null +++ b/data/38/3D/13/383D13A64823382BAB67404BBA514EEF.xml @@ -0,0 +1,114 @@ + + + +Catalogue of Geadephaga (Coleoptera, Adephaga) of America, north of Mexico + + + +Author + +Bousquet, Yves +Agriculture and Agri-Food Canada, Central Experimental Farm, Ottawa, Ontario, Canada +bousquety1@yahoo.com + +text + + +ZooKeys + + +2012 + +2012-11-28 + + +245 + + +1 +1722 + + + + +http://dx.doi.org/10.3897/zookeys.245.3416 + +journal article +http://dx.doi.org/10.3897/zookeys.245.3416 +1313-2970-245-1 +FFFF52503A0AFF882450FFB66D45FF8E +578462 + + + + +Bembidion nubiculosum Chaudoir, 1868 + + + + +Ochthedromus laticollis +LeConte, 1852a: 187 [secondary homonym of + +Bembidion laticolle + +(Duftschmid, 1812)]. Type locality: "Colorado [River, California]" (original citation). Lectotype (♂), designated by Erwin (1984a: 177), in MCZ [# 5523]. + + +Bembidium nubiculosum +Chaudoir, 1868b [July]: 244. Replacement name for + +Bembidium laticolle + +(LeConte, 1852). + + +Bembicidium platyderum +Gemminger and Harold, 1868a [August]: 418 [primary homonym of + +Bembidium platyderum + +Chaudoir, 1868]. Replacement name for + +Bembicidium laticolle + +(LeConte, 1852). + + +Ochthedromus pardalis +Zimmermann [in LeConte], 1869b: 247. Replacement name for + +Ochthedromus laticollis + +LeConte, 1852. + + +Bembidion nubiculosum daphnis +Casey, 1918: 120. Type locality: "El Paso [El Paso County], Texas" (original citation). Lectotype (♂), designated by Erwin (1984a: 177), in USNM [# 37036]. Synonymy established by Erwin (1984a: 177). + + +Bembidion amnicum +Casey, 1918: 121. Type locality: "Brownsville [Cameron County], Texas" (original citation). Lectotype (♂), designated by Erwin (1984a: 178), in USNM [# 37037]. Synonymy established by Erwin (1984a: 178). + + + +Distribution. + +This species is found from the Baja California Peninsula (Horn 1894: 308) and southeastern California (Casey 1918: 120; Andrews et al. 1979: 28) to southeastern Texas (Snow 1906a: 141; Casey, 1918: 121, as + +Bembidion amnicum + +) and northern Mexico (Erwin 1984a: 178). The record from +"Utah" +(Hayward 1897: 96) needs confirmation. + + + +Records. + +USA +: AZ, CA, NM, TX [UT] - Mexico + + + + \ No newline at end of file diff --git a/data/38/3D/6D/383D6DAB831C3846E1F432A1AA221249.xml b/data/38/3D/6D/383D6DAB831C3846E1F432A1AA221249.xml new file mode 100644 index 00000000000..1d4c7e86794 --- /dev/null +++ b/data/38/3D/6D/383D6DAB831C3846E1F432A1AA221249.xml @@ -0,0 +1,50 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Venus phryne +[ +spec. nov. +] + + + + +V. testa subcordata laevi antice posticeque transverse striata, ano obcordato venis violaceis. +M. L. U. + + + + +Habitat in +O. australiore. + + + + \ No newline at end of file diff --git a/data/38/3D/87/383D87C9FFADFFB0D4A3F9F1FB87FE22.xml b/data/38/3D/87/383D87C9FFADFFB0D4A3F9F1FB87FE22.xml new file mode 100644 index 00000000000..23e7da3ac50 --- /dev/null +++ b/data/38/3D/87/383D87C9FFADFFB0D4A3F9F1FB87FE22.xml @@ -0,0 +1,301 @@ + + + +A new species of the genus Sovia Evans, 1949 from South Central Yunnan, China (Lepidoptera, Hesperiidae) + + + +Author + +Huang, Si-Yao + + + +Author + +Wang, Xin-Yue + + + +Author + +Fan, Xiao-Ling + +text + + +Zootaxa + + +2020 + +2020-02-10 + + +4731 + + +4 + + +565 +573 + + + +journal article +24091 +10.11646/zootaxa.4731.4.9 +04de1a71-1492-4258-af1b-3220d16bfc6f +1175-5326 +3662016 +F6AEAFDF-755C-4805-8EB8-A3DCF53BA003 + + + + + + + +Sovia liuzihaoi +Huang & Fan + +sp. nov. + + + + + + +( +Figs. 2–5 +, +10–11 +, +15 +) + + + + +Type material. + + +Holotype +: + + +, altitude ca. + +2100 m + +, + +3. VIII. 2018 + +, +Mt. Ailao +, +Xinping Yi +and +Dai Autonomous County +, Yuxi City, +Yunnan Province +, P. +R +. +China +, leg. +Si-yao Huang +, HSY001 ( +SCAU +) + +. + + +Paratype +: + +1 ♂ +, same data as holotype, HSY002 ( +SCAU +) + +; + +1 ♂ +, same data as holotype ( +SCAU +) + +. + + + + +Diagnosis. + +S. liuzihaoi + + +sp. nov. + +can be distinguished from congeners by forewing upperside with only two subapical spots, male stigma linear, extremely narrow, male genitalia uncus expanded subapically in dorsal view and outer lower angle of valva protruding and forming a perpendicular angle. + + + + + +Description. Male ( +Figs. 2–5 +). + +Forewing length +15–16 mm +( +16 mm +in +holotype +). Compound eyes black. Antennae longer than half of the length of forewing. Head covered by yellowish-green hair dorsally. Labial palpi with second segment porrect and covered with yellowish green hair and scales thoroughly; third segment porrect and covered by yellowish green scales ventrally, ending with a blunt tip. Thorax black dorsally and covered by yellowish green hair ventrally. Abdomen black dorsally and covered by pale scales ventrally. Forewing upper side ground color blackish brown, costa scattered with yellowish green scales from base and ending before middle point. Upper side all patterns pale yellowish white; discal cell with cell spot rectangular and narrow; subapical area with two spots in cells R +4 +and R +5 +; cell M +3 +with a small rounded spot; cell Cu +1 +with a large rectangular spot at base. Stigma linear, pale whitish, not continuous in the middle and presenting at base of cell Cu +2. +Cilia clearly chequered with yellowish white and dark brown. Forewing under side yellowish at costa, blackish brown from base to discal zone and reaching outer margin, pale grey at dorsumal area, patterns similar to upper side. Hindwing upper side ground color same as in forewing, becoming paler at costal area and without any markings, cilia same as forewing. Hindwing under side ground color greenish yellow, paler near dorsumal area. + + + +FIGURES 2–9. +Male adults of + +Sovia + +spp. 2–3, + +S. liuzihaoi + + +sp. nov. + +, holotype, Mt. Ailao, Xinping County, HSY001; 4–5, +ditto +, paratype, Mt. Ailao, Xinping County, HSY002; 6–7, + +S. separata magna +(Evans) + +, Baihualing, Baoshan City, HSY003; 8–9, + +S. lii +Xue + +, paratype, Qinghe, Kang County, HSY005. Scale=1 cm. + + + + +Male genitalia ( +Figs. 10–11 +). + +Uncus long, broad and generally arrow-shaped, with the distal half gradually broadening subapically in dorsal view and abruptly narrowing towards apex and ending with a triangular tip. Tegumen nearly rounded in dorsal view, about half of the length of uncus. Lateral process of tegumen digital in lateral view. Gnathos slightly sclerotized at lateral wall, bifid in ventral view; each branch with basal one third strongly slcerotized and distal two thirds covered by numerous spinules. Saccus short, nearly triangular. Valva broad, with its outer lower angle of valva protruding and forming a perpendicular angle; dorsobasal process strongly sclerotized, trapezoid, with a small projection at the base; dorsodistal process strongly sclerotized, small and parallelogramshaped; ventrobasal process strongly sclerotized, rather broad and nearly trapezoid; ventrodistal process strongly sclerotized and nearly rectangular, with its inner ventral angle extending inward; its dorsal margin covered by numerous dentation of various shape and its outer margin covered by smaller dentation; the inner projection of ventrodistal process broad and robust, surrounded by large dentation. Juxta shallowly V-shaped. Aedeagus moderately long; its suprazonal sheath about two thirds of the length of subzonal sheath; the suprazonal sheath with its distal end expanding in dorsal view and its dorsal wall deeply concave. + + + +FIGURES 10–13. +Male genitalia of + +Sovia + +spp. 10–11, + +S. liuzihaoi + + +sp. nov. + +10, holotype, HSY001; 11, paratype, HSY002. 12, + +S. separata magna +(Evans) + +, HSY003; 13, + +S. lii +Xue + +, HSY005. a=genitalia capsule in lateral view with valvae removed; b=inner view of left valva; c=inner view of right valva; d=uncus and tegumen in dorsal view; e= uncus, gnathos and tegumen in ventral view; f=aedeagus in dorsal view; g=aedeagus in lateral view; h=juxta. Scale=1 mm. + + + + +FIGURES 14–15. +Habitat and alive male adult of + +Sovia liuzihaoi + + +sp. nov. + +14, collecting site in Mt. Ailao; 15, alive male adult resting on a cement block with wings unfolded. + + + +Female. +Unknown. + + + + +Distribution. +Currently this species is only known from its +type +locality, Mt. Ailao in South Central +Yunnan Province +, Southwestern +China +( +Fig. 16 +). + + + + +Etymology. +The specific name + +liuzihaoi + +is dedicated to Dr. Zi-hao Liu (University of Science and Technology of +China +, Hefei City, +Anhui Province +, P. R. +China +), an old friend of the first author and also a +Lepidoptera +enthusiast who keeping providing him with valuable material of butterflies and moths from other parts of +China +during the past ten years. + + + + +Biology. +This species is found near a stream surrounded by good vegetation at an altitude around +2100 m +( +Fig. 14 +). Males are very sensitive and flying swiftly when disturbed with typical territorial behavior, and usually resting on leaves of trees or brushes and cement blocks with wings unfolded ( +Fig. 15 +). + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFD07458FF27FE55FBF44DBB.xml b/data/38/3D/C5/383DC579FFD07458FF27FE55FBF44DBB.xml new file mode 100644 index 00000000000..639ee067443 --- /dev/null +++ b/data/38/3D/C5/383DC579FFD07458FF27FE55FBF44DBB.xml @@ -0,0 +1,203 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes tubesauassu + +, +new species + + + +(figs. 4, 18, 30) + + + +Holotype +: soldier, part of lot MZUSP-10160, +13 +.xii.1990, E.M. Cancello & M.T. Ponte coll. + + +Type-locality: +Brazil +: Bahia State, Andaraí. ( +17º49' 48" S +, +52º 30' W +) + + +Paratypes +: +BRAZIL +. +Bahia +: Vitória da Conquista: +30.vi.1970 +, R.L. Araujo coll. (4810); Andaraí: 12, +13 +.xii.1990, E.M. Cancello & M.T. Ponte coll. (10160*, 10161). +Minas Gerais +: Curvelo: +15.xi.1972 +, R.L. Araujo coll. (5582); Francisco Sá: +17.vii.1975 +. (5938, 5980). +Paraíba +: João Pessoa, +Mata +do Buraquinho: +1– 20.vi.2000 +, A. Vasconcellos coll. (11481). +Rio de Janeiro +: Rio de Janeiro, Jardim Zoológico: +6.i.1966 +, R.L. Araujo coll. (376). + + + + +Etymology: + +tubesauassu + +from Tupi “Tuba” (=father) “Esá” (=eye) and “-ûaçu” (suffix for large) in reference to imago eyes’ large size. In the latinized form, “ç” is converted to “ss”. + +Imago. Eyes large, distant from the inferior margin of head by less than the larger diameter of the ocellus. Ocelli in dorsal view reniform and large, oval and remote from the eye by distance less that its minimum diameter in lateral view. Fontanelle broad and small. Head capsule covered by short hairs, scattered bristles. Labrum with bristles in two rows. Pronotum covered with denser short hairs and bristles. Mesonotum and metanotum with short hairs, concentrated on the center and posterior margins. Head sepia brown to brown, pronotum and tergites brown to pale brown, sternites pale yellow, legs pale brown and wing scales brown. + +Comparisons. +The imago of + + +O +. tubesauassu + + + +sp. nov. + +differs from those of other species by the combination of large eyes and small fontanelle. The most similar species are + + +O +. aduncus + + +and + + +O +. wheeleri + + +, from which it differs by the small fontanelle. + +Soldier. Head sides parallel in dorsal view, flanges whit a distinct slight constriction. In profile dorsal lump salient, behind the flanges. Mandibles of the first pattern (see Material and Methods), tooth-like projection at half. Head capsule with short hairs, denser on ventral surface, and scattered bristles, microscopic hairs on entire head. Posmentum with bristles. Pronotum with short hairs and bristles, more abundant on margins. Mesonotum and metanotum with bristles on posterior margins. Abdominal tergites densely covered with bristles. Sternites covered with short hairs and erect bristles on posterior margins. + +Comparisons. + + +O +. tubesauassu + + + +sp. nov. + +soldier has a head capsule larger than + + +O + +. +mirim + + +sp. nov. + +, + + +O + +. +pilosus + + +sp. nov. + +, and smaller than + + +O +. humilis + + +. The most similar species is + + +O + +. +aduncus + +whose flanges do not have a slight constriction at the base. + + +Geographical Distribution (fig. 30). + + +O +. tubesauassu + + + +sp. nov. + +is recorded from rain forest and seasonal semi-deciduous forest (both inside the domain of the Atlantic Forest), from Cerrado vegetation (Curvelo, state of Minas Gerais) and Caatinga vegetation (Francisco Sá, state of Minas Gerais). + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFD0745BFF27F91DFF7049F1.xml b/data/38/3D/C5/383DC579FFD0745BFF27F91DFF7049F1.xml new file mode 100644 index 00000000000..3ad5447e97e --- /dev/null +++ b/data/38/3D/C5/383DC579FFD0745BFF27F91DFF7049F1.xml @@ -0,0 +1,135 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes uncimandibularis + +, +new species + + + +(figs. 11, 32) + + + +Holotype +: soldier, part of lot MZUSP-8352, +20 +.iii.1977, A. Bandeira coll. + + +Type-locality: +Brazil +: Amazonas State, Manaus/Boa Vista Road (BR- 174, km 31). + + +Paratypes +: +BRAZIL +. +Amazonas +: Manaus/Boa Vista (Km 31): +20.iii.1977 +, A. Bandeira coll. (8352); BR- 174, Km 54: +5.viii.2000 +, I. Ackerman coll. (INPA-0003) +6.v.2002 +. (INPA-02014, INPA-02017); +7.vii.2002 +. (INPA-02028); +5.vi.2002 +. (INPA-02079); Manaus: +1.iii.1997 +, E. Barros coll. (UnB-2007). + + + + +Etymology: + +uncimandibularis + +is a combination of the words “ +unci +” (= hook) and “ +mandibula +” (= mandible), from Latin, in reference to the curved tip of left mandible, like a hook. + +Imago. Unknown. +Soldier. Head with sides slightly convergent in front in dorsal view. In profile dorsal lump slightly salient, behind the flanges. Mandibles of the second pattern, left mandible with the tip strongly curved, like a distinct terminal hook, and tip of the right mandible forming a 90º angle with proximal portion of mandible, tooth-like projection at proximal half. Head capsule with sparse bristles and short hairs, denser on ventral surface, scattered microscopic hairs on entire head capsule and denser in distal region. Posmentum with bristles. Pronotum with short hairs on surface and bristles on margins. Mesonotum and metanotum with bristles on posterior margins. Abdominal tergites and sternites densely covered with bristles, erect bristles on posterior margins. + +Comparisons. + + +O +. uncimandibularis + + + +sp. nov. + +soldier differs from all other species by the pronounced terminally curved tip of left mandible, like a hook. + + + + +Geographical distribution. +All records of + + +O +. uncimandibularis + + + +sp. nov. + +are in Amazonian forest ( +Fig. 32 +). + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFD17458FF27FA09FA9A4A72.xml b/data/38/3D/C5/383DC579FFD17458FF27FA09FA9A4A72.xml new file mode 100644 index 00000000000..740b941deda --- /dev/null +++ b/data/38/3D/C5/383DC579FFD17458FF27FA09FA9A4A72.xml @@ -0,0 +1,135 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes pilosus + +, +new species + + + +(figs. 6, 31) + + + +Holotype +: soldier, identified as such, part of lot MZUSP-0323, +20.ii.1947 +, Helmut Sick coll. + + +Type-locality: +Brazil +: Mato Grosso State, Xavantina. ( +14º 39’ S +, +52º 21’ W +) + + +Paratypes +: +BRAZIL +. +Mato Grosso +: Chapada dos Guimarães: +10.ii.1976 +, R.L. Araujo coll. (6782, 6813, 6832); Coxipó: 14, 18, +17.ii.1976 +(6662, 6687, 6704, 6855); Cuiabá 14 Km ao NO: +15.ii.1976 +(6530); Poconé, research base +IBDF +: +16.ii.1994 +, M.A. Drumond coll. (11465); Xavantina: +20.ii.1947 +, Helmut Sick coll. (323). + + + + +Etymology: + +pilosus + +(=hairy), from Latin, in reference to the denser short hairs that cover entire head. + +Imago. Unknown. +Soldier. Head sides parallel in dorsal view. In profile dorsal lump slightly salient, behind the flanges. Mandibles of the first pattern (see Material and Methods), tooth-like projection at half. Head capsule with denser short hairs on all surfaces and scattered bristles. Posmentum with short hairs and bristles. Pronotum with short hairs and bristles on margins, mesonotum and metanotum with bristles on posterior margins, abdominal tergites densely covered with bristles and short hairs, sternites covered with short hairs and erect bristles on posterior margins. + +Comparisons. + + +O +. pilosus + + + +sp. nov. + +differs from all other species with the same mandible patterns by the head capsule covered with denser short hairs. + + + + +Geographical distribution. +All registers of + + +O +. pilosus + + + +sp. nov. + +are in open formations ( +Fig. 31 +). + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFD17459FF27FDD1FE354E59.xml b/data/38/3D/C5/383DC579FFD17459FF27FDD1FE354E59.xml new file mode 100644 index 00000000000..95fc13354be --- /dev/null +++ b/data/38/3D/C5/383DC579FFD17459FF27FDD1FE354E59.xml @@ -0,0 +1,189 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes orthognathus +(Silvestri) + + + + +(figs. 12, 30) + + + + + +Capritermes orthognathus + +Silvestri, 1903 +:65 + + +(soldier, 114); + +Capritermes paradoxus + +Silvestri, 1901 +:5 + + +(misidentification); + +Termes (Eutermes) orthognathus + +; + +Desneux 1904 +:44 + +; + + + + + +Orthognathotermes orthognathus + +; + +Holmgren, 1912 +:119 + +. + + + + + +Syntypes +: DEZA, not examined, and MZUSP soldiers and workers. +PARAGUAY +. Tacurú-Pucu: +3.vii.1900 +, Fillippo Silvestri coll. (2011). Examined. + +Imago. Unknown. +Soldier. Head sides parallel in dorsal view. In profile dorsal lump slightly salient behind the flanges. Mandibles of the second pattern, tooth-like projection at proximal half. Head capsule with sparse bristles and short hairs, denser on ventral surface, scattered microscopic hairs on entire capsule and denser in distal region. Posmentum with bristles and short hairs. Pronotum with short hairs and bristles, more abundant on margins. Mesonotum and metanotum with bristles and short hairs on posterior margins. Abdominal tergites and sternites densely covered with bristles. Sternites with erect bristles on posterior margins. + +Comparisons. + + +O +. orthognathus + + +soldier has robust mandibles, a head capsule larger than + + +O +. brevipilosus + +, + +O +. longilamina + + + +sp. nov. + +, + + +O +. macrocephalus + +, + +O +. okeyma + + + +sp. nov. + +, and parallel head capsule sides (slightly convergent in front in + + +O +. insignis + + +and + + +O +. uncimandibularis + + + +sp. nov. + +). The most similar species is + + +O + +. +heberi + +, whose soldiers have narrower mandibles. + + +Geographical distribution. +The unique register for + + +O +. orthognathus + + +is the type-locality, in Cerrado formation ( +Fig. 29 +). + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFD3745BFF27FCE1FE484CAD.xml b/data/38/3D/C5/383DC579FFD3745BFF27FCE1FE484CAD.xml new file mode 100644 index 00000000000..d16ad3d86f5 --- /dev/null +++ b/data/38/3D/C5/383DC579FFD3745BFF27FCE1FE484CAD.xml @@ -0,0 +1,149 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes wheeleri +Snyder + + + + +(figs. 3, 17, 30) + + + + + +Orthognathotermes wheeleri + +Snyder, 1923 +:129 + + +(soldier, 1); + + + + + +Orthognathotermes wheeleri + +; + +Nickle & Collins, 1992 +:230 + +, 231 (soldier, 68,69). + + + + + +Holotype +: +NMNH +(soldier), not examined. + +Imago. Eyes large, distant from the inferior margin of head by less than the larger diameter of the ocellus. Ocelli in dorsal view semicircular, oval and remote from the eye by a distance less that its minimum diameter in lateral view. Fontanelle broad and medium-sized. Head capsule with few short hairs, fewer on ventral surface, scattered bristles only on dorsal surface. Labrum with bristles not organized in rows. Pronotum denser covered with bristles and short hairs. Mesonotum and metanotum covered by short hairs, concentrated in the center and margins. Head sepia brown, pronotum pale brown and tergites brown to pale brown, sternites yellow, legs and wing scales pale brown. + +Comparisons. +The imago of + + +O +. wheeleri + + +differs from those of other species by the large eyes and medium fontanelle. The most similar species is + + +O +. aduncus + + +, from which it differs by the ocelli touching the eye in lateral view. + +Soldier. Head with parallel sides in dorsal view. In profile dorsal lump salient, behind the flanges. Mandibles of the first pattern, tooth-like projection at proximal half. Ocellar spots visible. Head capsule with short hairs and sparse bristles, denser on ventral surface, scattered microscopic hairs sparce on entire head. Posmentum with bristles and short hairs. Pronotum with short hairs and bristles on surface, denser on margins. Mesonotum and metanotum with bristles on posterior margins. Abdominal tergites densely covered with short hairs and bristles. Sternites covered with short hairs, bristles on posterior margins. + +Comparisons. + + +O +. wheeleri + + +soldier differs from all other + +Orthognathotermes + +species by the visible ocellar spots. + + + + +Geographical distribution. +Known only from two localities in +Panama +, the northernmost distribution of the genus. + + + + +Comments. +We prefer to use the term "ocellar spot" instead of "eye spot", as used by +Snyder (1923) +, since this structure (similar to ocellus) is placed where the ocellus is usually placed in alate's head. + + + + +Material examined. +PANAMA +. La jagua hunting Club, 6 Milles S.E. of Pacorá: +26.v.1935 +, A.E. Emerson coll. (3690*, 4389*). + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFD4745CFF27FE01FCCE4CFC.xml b/data/38/3D/C5/383DC579FFD4745CFF27FE01FCCE4CFC.xml new file mode 100644 index 00000000000..b23a26f9b2e --- /dev/null +++ b/data/38/3D/C5/383DC579FFD4745CFF27FE01FCCE4CFC.xml @@ -0,0 +1,267 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes longilamina + +, +new species + + + +(figs. 14, 23, 32) + + + +Holotype +: soldier identified as such, part of lot MZUSP-9819, +28 +.i.1993, E.M. Cancello & B.A. +O +. da Silva coll. + + +Type-locality: +Brazil +: Espírito Santo State, Linhares. ( +18º 42’ 54’’ S +39º 51’ 12’’ W +) + + +Paratypes +: +BRAZIL +. +Bahia +: Milagres - Jequié: +22.vii.1974 +, R.L. Araujo coll. (5550); Maracás: +26.xi.1990 +, E.M. Cancello & M.T. Ponte coll. (10159). +Espírito Santo +: Linhares: +28.i.1993 +, E.M. Cancello & B.A. +O +. da Silva coll. (9819*, 9820, 9821). +Minas Gerais +: Belo Horizonte: +1.xii.1956 +, R.L. Araujo coll. (2012); +4.i.1954 +. (4067); +1.xii.1956 +, (4529*); +28.xi.1956 +.; (4707); +9.vii.1975 +. (6088); +12.vii.1975 +. (6230); BR 135, Km 14 (near Belo Horizonte): +17.viii.1971 +. (4936); BR 135, (ca 16 Km S de Belo Horizonte): +13.ii.1972 +. (5011); Campos Altos: +11.xi.1972 +. (5744); Capitão Enéias: +15.vii.1975 +. (6251); Lagoa Santa: +12.i.1954 +. (4104, 4106); +20.xi.1972 +. (5667); Montes Claros: +23.vii.1975 +(6165); Poços de Caldas: +13.ix.1967 +(434); Teófilo Otoni: +28.vi.1970 +(4793); Jatiboca, Faz. Decima: +1.xi.1995 +, no collector data. (UFV-1040); Jatiboca, Pombal: 1996, no collector data (UFV-841); Jatiboca, São Bento: 1996, no collector data (UFV-1703); Lagoa Santa, +PAMA +: +20.x.1993 +, Denize coll. (UFV-3524); Sete Lagoas: +13.v.1982 +, D.L. Domingos & T.M.C.M. Cavernaghi coll. (UFV-5451, UFV-5454); +22.ix.1982 +. (UFV-5452); +9.xi.1984 +(UFV-5458); Parque do Rio Doce: +11.x.1994 +, Júlio coll. (UFV-4962); +28.iii.1985 +(UFV-6265). +Paraíba +: João Pessoa, +Mata +do Buraquinho: +1–20.vi.2000 +, A. Vasconcellos coll. (11478, 11479). +Pernambuco +: Recife, Horto dois irmãos: +1– 20.vi.2000 +, M.P. Silva coll. (11480). +Piauí +: Francisco Santos: +7.xii.1976 +, R.L. Araujo coll. (7126). +Rio de Janeiro +: Campos: +5.ix.1963 +, M.M. Chaves coll. (2007); +Tocantins +: Jalapão: +13.ii.2002 +, D. Mesquita coll. (UnB-3497). + + + + +Etymology: + +longilamina + +is the combination of the words “ +longi +” (=long) and “ +lamina +” (=blade), from Latin, in reference to the distal long cutting edge on inner margin of mandible, in comparison to rod-like basal part. + +Imago. Unknown. +Soldier. Head with sides irregular and slightly convergent in front in dorsal view. In profile dorsal lump slightly salient, behind the flanges. Mandibles of the second pattern, tooth-like projection at proximal half. Head capsule with scattered bristles and short hairs, denser on ventral surface, microscopic hairs in distal region. Posmentum with bristles. Pronotum with short hairs and bristles, more abundant on margins, mesonotum and metanotum with bristles on posterior margins, abdominal tergites and sternites densely covered with bristles, sternites with erect bristles on posterior margins. + +Comparisons. + + +O +. longilamina + + + +sp. nov. + +soldier has mandibles of the second pattern, a head capsule smaller than + + +O +. gibberorum + + +, + + +O +. heberi + + +, + + +O +. insignis + + +, + + +O + +. +okeyma + + +sp. nov. + +, + + +O +. orthognathus + + +, + + +O +. uncimandibularis + + + +sp. nov. + +and differs form all other species by the distal long slender cutting edge on inner margin of mandible. The most similar species are + + +O + +. +macrocephalus + +, from which it differs by the curved lateral margins of head capsule, and + + +O +. brevipilosus + + +, from which it differs by the denser short hairs on ventral surface of head capsule. + + + + +Geographical distribution. +Records of + + +O +. longilamina + + +are in open formations, like pastures, Cerrados and Caatinga, and in closed forest formations (Atlantic Forest). + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFD5745CFF27FD1FFA8F4A4D.xml b/data/38/3D/C5/383DC579FFD5745CFF27FD1FFA8F4A4D.xml new file mode 100644 index 00000000000..e1aab98df22 --- /dev/null +++ b/data/38/3D/C5/383DC579FFD5745CFF27FD1FFA8F4A4D.xml @@ -0,0 +1,273 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes insignis +Araujo + + + + +(figs. 7, 20, 25–26, 28, 29, 36, 37) + + + + + +Orthognathotermes insignis + +Araujo, 1977 +:75 + + +(Imago and soldier, 1–16). + + + + + +Holotype +: +MZUSP +(soldier: MZUSP-3271, +Brazil +, São Paulo, São Paulo (Morumbi), +13.xi.1950 +, R.L. Araujo coll.), examined. + + +Paratypes +: soldier, workers and imagos. +BRAZIL +. +São Paulo +: Atibaia: +19.iii.1946 +, R.L. Araujo coll. (2934); Jarinú: +2.iii.1945 +, V. Autuori coll. (2839); Louveira: +ix.1926 +, Oliveira Filho coll. (156); Osasco: +5.vi.1951 +, R.L. Araujo coll. (3357); Santo Amaro: +17.iv.1951 +, (3333, 3335); São Paulo: +30.viii.1944 +, (2381); +14.iii.1945 +. (2845); +8.x.1948 +. (3122, 3123*, 3125*); +31.x.1950 +. (3256, 3268*, 3270*-3274*); +20.iii.1951 +. (3319-3325); +9.v.1951 +. (3344); +22.v.1951 +. (3350); São Paulo (Ibirapuera): +xi.1944 +. (2703); +25.ix.1945 +. (2906); +10.v.1946 +. (2954); São Paulo (Ipiranga): no data, F. Silvestri coll. (2008). All examined. + +Imago. Eyes small, distant from the inferior margin of head equal to the larger diameter of the ocellus. Ocelli in dorsal view reniform and narrowed, sub-triangular and remote from the eye by distance less that its minimum diameter in lateral view. Fontanelle broad and large. Head capsule covered by short hairs, less on ventral surface, scattered bristles. Labrum with bristles not organized in rows. Pronotum densely covered with bristles and short hairs. Mesonotum and metanotum covered by short hairs, concentrated in the center and margins. Head sepia brown, pronotum brown to sepia brow and tergites brown to pale brown, sternites yellow, legs and wing scales pale brown. + +Comparisons. +The imago of + + +O +. insignis + + +differs from those of the other species by the combination of subtriangular ocelli in lateral view and large fontanelle. The most similar species are + + +O +. heberi + + +and + + +O +. longilamina + + + +sp. nov. + +, from which they differ by the ocelli more distant from the eyes. + +Soldier. Head with sides slightly convergent in front; in dorsal view. In profile dorsal lump slightly salient, behind the flanges. Mandibles of the second pattern (see Material and Methods), tooth-like projection at half. Head capsule with short hairs and sparse bristles, scattered microscopic hairs on back. Posmentum with bristles and short hairs. Pronotum with short hairs on the surface and bristles on margins, mesonotum and metanotum with bristles on posterior margins, abdominal tergites densely covered with short hairs and bristles, sternites covered with short hairs, bristles on posterior margins. + +Comparisons. + + +O +. insignis + + +soldier has a head capsule larger that + + +O +. brevipilosus + +, + +O +. longilamina + + + +sp. nov. + +, + + +O +. macrocephalus + +, + +O +. okeyma + + + +sp. nov. + +and slightly convergent to front head capsule sides (parallel on + + +O +. heberi + + +, + + +O + +. +gibberorum + +and + + +O +. orthognathus + + +). The most similar species are + + +O +. uncimandibularis + + + +sp. nov. + +, whose soldiers differ by its strongly hooked tip on the left mandible and + + +O +. heberi + +, + +whose soldiers have the head sides parallel. + + + + +Geographical distribution. +All registers of + + +O +. insignis + + +are in open formations ( +Fig. 29 +). + + + + +Material examined. +BRAZIL +. +Bahia +: Vitória da Conquista: +30.vi.1970 +, R.L. Araujo coll. (4800). +Minas gerais +: Parque da Canastra: +26.viii.1990 +, M.A. Drumond coll, (9523*, 11473); Poços de Caldas: +24.xii.1966 +, R.L. Araujo coll. (414); +25.xii.1966 +. (415-417); 3, 6, 10, 14-16, +18 +.ix.1967. (435, 437-440, 441*, 442-450, 452, 453, 516, 451); Sete Lagoas, +24.vi.1982 +, D.J. Domingos coll. (UFV-5447). +São Paulo +: Botucatu: +26.iv.2001 +, E.M. Cancello & C. Bordereau coll. (11474); Jarinú: +25.ii.1945 +, R.L. Araujo coll. (4322). + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFD67459FF27FC0CFA834AFE.xml b/data/38/3D/C5/383DC579FFD67459FF27FC0CFA834AFE.xml new file mode 100644 index 00000000000..53788936f97 --- /dev/null +++ b/data/38/3D/C5/383DC579FFD67459FF27FC0CFA834AFE.xml @@ -0,0 +1,229 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes okeyma + +, +new species + + + +(figs. 13, 22, 30) + + + +Holotype +: soldier, part of lot MZUSP-8430, +28 +.iii–6.iv.1984, Exp. MZ-IQUSP coll. + + +Type-locality: +Brazil +: Goiás State, Parque Nacional das Emas ( +17º 49' 48" S +, +52º 30' W +). + + +Paratypes +: +BRAZIL +. +Goiás +: Parque Nacional das Emas: +28.iii–6.iv.1984 +, Exp. MZ-IQUSP coll. (8430, 8431); +12.vi.1980 +, K.H. Redford coll. (9771, 10821*); +15–19.xii.1987 +, Exp. MZ-IQUSP coll. (11476); +ix.1981 +, K.H. Redford coll. (11477); +15-17 +, 21, +23.i.2004 +, D.A. Costa coll. (12126, 12127, 12128*, 12129*, 12130, 12131, 12132, 12139, 12140, 12149, 12150, 12151, 12152, 12153); 14,18-20, 22, 25, +26 +.iv.2004, D.A. Costa coll. (12125, 12133, 12134, 12135*, 12136, 12137, 12138, 12141*, 12142, 12143, 12144, 12145, 12146, 12147, 12148, 12154, 12155); Santo Antônio de Goiás (Embrapa): +5.v.2000 +, K. Espírito-Santo Filho coll. (12156); +13.iv.1980 +, K.H. Redford coll. (MPEG-1272). +Mato Grosso do Su +l: Campo Grande: +20.ii.1976 +, R.L. Araujo coll. (6569). + + + + +Etymology: +“ + +okeyma + +” (homeless) from Tupi, in reference to fact that all samples of this species have been collected in other termites species nests. + +Imago. Eyes small, distant from the inferior margin of head by a distance equal to the larger diameter of the ocellus. Ocelli in dorsal view reniform and narrowed, oval and remote from the eye by distance equal to its minimum diameter in lateral view. Fontanelle narrow and small. Head capsule covered with short hairs, scattered bristles. Labrum with bristles not organized in rows. Pronotum covered with short hairs and bristles on margins. Mesonotum and metanotum covered by short hairs, concentrated in the center and posterior margins. Head, pronotum and tergites brown to sepia brown, sternites and legs pale brown and wing scales sepia brown. + +Comparisons. +The imago of + + +O +. okeyma + + + +sp. nov. + +differs from those of the other species by the combination of small eyes and small fontanelle. The most similar species is + + +O +. mirim + + + +sp. nov. + +, from which it differs by the labrum bristles (not organized in rows). + +Soldier. Head sides parallel in dorsal view. In profile dorsal lump slightly salient, behind the flanges. Mandibles of the second pattern, tooth-like projection at proximal half. Head capsule with scattered short hairs and bristles, denser on ventral surface, scattered microscopic hairs on entire head capsule and denser in distal region. Posmentum with shot hairs and bristles. Pronotum with short hairs and bristles, more abundant on margins, mesonotum and metanotum with bristles and short hairs on posterior margins, abdominal tergites and sternites densely covered with bristles, sternites covered with erects bristles on posterior margins. + +Comparisons. + + +O +. okeyma + + + +sp. nov. + +soldier has robust mandibles, a head capsule smaller than + + +O +. heberi + + +, + + +O +. insignis + + +, + + +O +. orthognathus + + +, + + +O +. gibberorum + + +, + + +O +. uncimandibularis + + +and parallel head capsule sides (slightly convergent in front in + + +O +. brevipilosus + + +and + + +O +. longilamina + + + +sp. nov. + +). The most similar species is + + +O +. orthognathus + + +, whose soldier is larger. + + + + +Geographical distribution. +All registers of + + +O +. okeyma + + + +sp. nov. + +are in open formations ( +Fig. 29 +). + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFD7745EFF27FC6EFAA34854.xml b/data/38/3D/C5/383DC579FFD7745EFF27FC6EFAA34854.xml new file mode 100644 index 00000000000..ba3760cfe09 --- /dev/null +++ b/data/38/3D/C5/383DC579FFD7745EFF27FC6EFAA34854.xml @@ -0,0 +1,258 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes mirim + +, +new species + + + +(figs. 5, 19, 31) + + + +Holotype +: soldier, part of lot MZUSP-4056, +4 +.i.1954, R.L. Araujo coll. + + +Type-locality: +Brazil +: Minas Gerais State, Belo Horizonte. ( +20º 54' 36" S +, 47º W) + + +Paratypes +: +BRAZIL +: +Distrito Federal +: +Brasília +: 1970, K. Kitayama coll. (6996); Fazenda Agua Limpa: +19.ii.1986 +, R. Constantino coll. (MPEG-2622); +4.x.1999 +, (UnB-1890*); +19.vii.1981 +, I. Egler coll. (UnB- 1105); +1.viii.1982 +, (UnB-1109); +1.xi.1985 +(UnB-1106); 1993, K. Kitayama coll. (UnB-1107, UnB-1112); +10.v.1993 +, Suzana coll. (UnB-1120, UnB-1126); +7.v.1993 +, (UnB-1113); +16.xii.1993 +(UnB-1114); +28.v.1993 +, Carlos coll. (UnB-1119); +30.ix.1993 +, (UnB-1123); +21.xii.1992 +, Marcelo Lima coll. (UnB-1122); Planaltina - +CPAC +: +16.iv.1998 +, V.S. Dias coll. (UnB-941, UnB-943, UnB-947); Reserva Ecológica do +IBGE +: +18.ix.1998 +, R. Constantino coll. (UnB-1301). +Goiás +: Alexania: +25.x.1973 +, A.C. Santos coll. (7368); Cristalina: +11.iv.1991 +, D. Brandão coll. (UFG-399); Fazenda São Cipriano: +26.x.2001 +, R. Constantino coll. (UnB-3028); Parque Nacional das Emas: +28.iii-6.iv.1984 +, Exp. MZ-IQUSP coll. (8427); 17, +24 +.i.2004, D.A. Costa coll. (12120, 12124); 19, 20, +25.iv.2004 +(12121, 12122, 12123); Pirenópolis: +26.vii.2004 +, G.F. Lima Filho coll. (12119). +Minas Gerais +: Belo Horizonte: +23.viii.1962 +, R.L. Araujo coll. (59); +4.i.1954 +(4056, 4058), +29.xi.1956 +(4498*); +16.viii.1971 +(4935); Bom Sucesso: +12.xi.1972 +, (5770); Campos Altos:, +12.xi.1972 +(5877); Campanha: +28.vii.1954 +, (4228); Curvelo: +15.ii.1972 +, (5084); Lagoa Santa: +3.i.1957 +, (4702); Lagoa Dourada: +29.vii.1975 +(6256); Fazenda Susano: +28.x.2001 +, R. Constantino coll. (UnB-3116, UnB-3150); Fazenda Rossato: +27.x.2001 +(3076); Francisco Sá: +16.vii.1975 +, R.L. Araujo coll. (5979); Paraopeba: +14.x.1993 +, Terezinha coll. (UFV-4828); São Sebastião do Paraiso: +23.ii.1945 +, R.L. Araujo coll. (4122); Uberlândia: +8.xi.1972 +, (5711). +São Paulo +: Araçatuba: +8.xii.1953 +, R.L. Araujo coll. (3991); Campinas: +17.i.1970 +(4751); Novo Horizonte: +24.xi.1944 +, R. Araujo & Silva coll. (11357); Pirassununga: +28.ix.1947 +, R.L. Araujo coll. (3876); Santo Amaro: +10.x.1950 +(3230); São José dos Campos: +26.v.1953 +(4321); São Paulo (Ipiranga): +6.xii.1907 +, Herman Luederwaldt coll. (10822, 10823). + + + + +Etymology: + +mirim + +(small) from Tupi, a Brazilian Indian language, in reference to soldier size, smaller than most other + +Orthognathotermes + +species. + +Imago. Eyes small, distant from the inferior margin of head, equal to the larger diameter of the ocellus. Ocelli in dorsal view reniform and narrow, oval and remote from the eye by distance equal to its minimum diameter in lateral view. Fontanelle narrow and small size. Head capsule covered by short hairs, scattered bristles. Labrum with bristles on two rows. Pronotum with short hairs and scattered bristles, mainly on the margins. Mesonotum and metanotum covered by short hairs, concentrated distally and on posterior margins. Head and pronotum sepia brown, tergites brown to pale brown, sternites pale brown to yellow, legs brown to pale brown, wing scales sepia brown. + +Comparisons. +The imago of + + +O +. mirim + + + +sp. nov. + +differs from those of the other species by the combination of small fontanelle and eyes. The most similar species is + + +O +. okeyma + + + +sp. nov. + +, from which it differs by the labrum with bristles in two rows. + +Soldier. Head sides parallel in dorsal view. In profile dorsal lump slightly salient, situated between the flanges. Mandibles of the first pattern, tooth-like projection at proximal half. Head capsule with sparse bristles, short hairs variable, from sparse on entire head capsule to denser only distally, scattered microscopic hairs on all surfaces. Posmentum with bristles and short hairs. Pronotum with bristles and short hairs on the surface, denser at margins. Mesonotum and metanotum with bristles and short hairs on posterior margins. Abdominal tergites densely covered with short hairs and bristles. Sternites covered with short hairs and erect bristles on posterior margins. + +Comparisons. + + +O +. mirim + + + +sp. nov. + +soldier has a head capsule smaller than all other species of the same mandible pattern and differs from all by the labrum without lobes. The most similar species is + + +O + +. +pilosus + + +sp. nov. + +whose soldier displays a head capsule covered with denser short hairs. + + + + +Geographical distribution. +All records of + + +O +. mirim + + + +sp. nov. + +are in open formations ( +Fig. 31 +). + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFD7745FFF27FF5FFC02486D.xml b/data/38/3D/C5/383DC579FFD7745FFF27FF5FFC02486D.xml new file mode 100644 index 00000000000..b8f446eaae5 --- /dev/null +++ b/data/38/3D/C5/383DC579FFD7745FFF27FF5FFC02486D.xml @@ -0,0 +1,118 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes macrocephalus +(Holmgren) + + + + +(figs. 15, 32) + + + + + +Mirotermes macrocephalus + +Holmgren, 1906 +:42 + + +(soldier, worker, T-U) + + + + + +Orthognathotermes macrocephalus + +Holmgren, 1912 +:119 + + +(mandibles, soldier, 84, 85) + + + +Syntypes +: NRM (soldiers and workers: NRM-no number, Mojos, Caupolican Province, +Bolivia +, +1904–1905 +, Nils Holmgren coll.), examined. + + + +Imago. Unknown. +Soldier. Head with sides slightly convergent in front in dorsal view. In profile dorsal lump slightly salient, behind the flanges. Mandibles of the second pattern (see Material and Methods), tooth-like projection at proximal half. Head capsule with sparse bristles and short hairs, denser on ventral surface, scattered microscopic hairs on entire head capsule. Posmentum with bristles. Pronotum with short hairs and bristles on margins, mesonotum and metanotum with short hairs on posterior margins, abdominal tergites covered with short hairs and bristles, sternites with short hairs and bristles on posterior margins. + +Comparisons. + + +O +. macrocephalus + + +soldier has a head capsule smaller than all other species with the same mandible pattern. The most similar species is + + +O + +. +longilamina + + +sp. nov. + +, whose soldiers have narrower mandibles and a weak constriction on the distal portion of head. + + +Geographical distribution. +Known only from the type-locality. + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFD87453FF27FB6EFDC14BE5.xml b/data/38/3D/C5/383DC579FFD87453FF27FB6EFDC14BE5.xml new file mode 100644 index 00000000000..8754bcaa82c --- /dev/null +++ b/data/38/3D/C5/383DC579FFD87453FF27FB6EFDC14BE5.xml @@ -0,0 +1,152 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes brevipilosus +Snyder + + + + +(figs. 9, 29) + + + + + +Orthognathotermes brevipilosus + +Snyder, 1926 +:70 + + +. + + + + + +Holotype +: +NMNH +(soldier: TYPE-00209, Rosário, +Bolivia +, +xi.1921 +, W.M. +Mann +coll.), examined. See comments below. + +Imago. Unknown. +Soldier. Head with sides slightly convergent in front in dorsal view. In profile dorsal lump slightly salient, behind the flanges. Mandibles of the second pattern, tooth-like projection at proximal half. Head capsule with sparse bristles on surface, denser short hairs on ventral surface and microscopic hairs on surface. Posmentum with denser bristles and short hairs on surface, pronotum with bristles on anterior and posterior margins, mesonotum and metanotum with bristles in posterior margin, abdominal tergites and sternites densely covered with bristles. + +Comparisons. + + +O +. brevipilosus + + +soldier has mandibles of the second pattern, a head capsule shorter than + + +O +. gibberorum + +, + +O +. heberi + + +, + + +O +. insignis + + +, + + +O + +. +orthognathus + +and + + +O +. uncimandibularis + + + +sp. nov. + +, and differs from all other species by the much denser short hairs only on the ventral surface of head, without bristles. + + + + +Geographical distribution. +Known only from the +type +locality. + + + + +Material examined. Comments. +The +holotype +does not correspond exactly to Snyder’s (1926) description, as he mentioned “numerous (denser) short hairs” on the head capsule, and we verified that this is true only on the ventral surface of the head capsule. Snyder mentioned “possible eye spots”, but we could not find any structure like this. The remaining description and the measurements fit the examined material. There was inside the flask a red label inscribed “ +Type +nº” without any number, although in Snyder’s description it was mentioned Cat. N o 27674, +U.S. +N.M. + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFD97450FF27F9F6FC914F72.xml b/data/38/3D/C5/383DC579FFD97450FF27F9F6FC914F72.xml new file mode 100644 index 00000000000..8308a2b4f91 --- /dev/null +++ b/data/38/3D/C5/383DC579FFD97450FF27F9F6FC914F72.xml @@ -0,0 +1,260 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes aduncus +Emerson + + + + +(figs. 2, 16, 30, 34, 35) + + + + + +Orthognathotermes aduncus +Emerson + +in + +Snyder, 1949 +:176 + +. + + + + + + + +Orthognathotermes macrocephalus + +; + +Emerson, 1925 +:451 + +–453 (Imago and soldier, 93, misidentification). + +Orthognathotermes aduncus + +; + +Mathews, 1977 +: 125 + +(Imago and soldier, 73, 74, redescription). + + + + + +Holotype +: +AMNH +(soldier), not examined. + + +Paratypes +: +AMNH +, not examined, and +MZUSP +soldiers, workers and imagos. +GUYANA +, Kartabo, +21.IV.1919 +, A. E. Emerson coll.(3689), examined. See comments below. + +Imago. Eyes large, distant from the inferior margin of head by less than the larger diameter of the ocellus. Ocelli in dorsal view semicircular, oval and touching the eyes in lateral view. Fontanelle broad and mediumsized. Head capsule covered by short hairs, bristles on dorsal face. Labrum with bristles on two rows. Pronotum with bristles and short hairs, mainly on the margins. Mesonotum and metanotum covered by dense bristles, concentrated in the center and posterior margins. Head brown, pronotum and tergites pale brown, sternites yellow, legs and wing scales pale brown. + +Comparisons. +The imago of + + +O +. aduncus + + +differs from those of the other known species by the combination of large ocelli, fontanelle and eyes. The most similar imago is + + +O +. wheeleri + + +, from which it differs by the labrum with dispersed bristles and more salient ocelli, not touching the eyes. + +Soldier. Head sides parallel in dorsal view. In profile dorsal lump salient, behind the flanges. Mandibles of the first pattern, tooth-like projection at proximal half. Head capsule with sparse bristles and short hairs denser in ventral surface, scattered microscopic hairs on all surfaces. Posmentum with bristles and short hairs. Pronotum with bristles and short hairs on the surface, mesonotum and metanotum with short hairs on posterior margins, abdominal tergites and sternites densely covered with short hairs and bristles on posterior margins. + +Comparisons. + + +O +. aduncus + + +soldier has mandibles of the first pattern, parallel head capsule sides and is larger than + + +O +. mirim + + + +sp. nov. + +and + + +O +. pilosus + + + +sp. nov. + +The most similar species are + + +O + +. +humilis + +, with larger soldier, + + +O + +. +tubesauassu + + +sp. nov. + +that has smaller flange narrower at base and + + +O + +. +wheeleri + +with visible ocellar spots. + + + + +Geographical distribution. +All registers for + + +O +. aduncus + + +are in Amazonian forest ( +Fig. 30 +). + + + + +Comments. +Emerson in +Snyder (1949) +mentioned that the " +Type +" is deposited at the AMNH, referring to material described by +Emerson (1925) +as + + +O +. macrocephalus + +, Kumar Krishna + +confirms to us that the “ +Type +” is a unique soldier under the label “ +holotype +soldier det & coll. Kartabo, +British Guiana +21.1 +V. 1919 +# 39A.” + + +Emerson (1925) +does not mention workers, although part of his material is deposited in MZUSP (3689) with workers. + + + + +Material examined. +BRAZIL +. +Amazonas +: Manaus/Itacoatiara (Km 232): +21.v.1977 +, A. Bandeira coll. (8351). +Pará +: Tucuruí (Rio Tocantins): +12.iv.1984 +, A.G. Bandeira coll. (MPEG-2072). +Roraima +: +Ilha +de Maracá: +21.xi.1978 +, A.G. Bandeira coll. (MPEG-3945). + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFD97451FF27FF5FFA294ED6.xml b/data/38/3D/C5/383DC579FFD97451FF27FF5FFA294ED6.xml new file mode 100644 index 00000000000..9360ca68bbd --- /dev/null +++ b/data/38/3D/C5/383DC579FFD97451FF27FF5FFA294ED6.xml @@ -0,0 +1,313 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes + +soldier key + + + + + + + + +1. In dorsal view, inner distal margin of the right mandible smoothly curving inward, in a continuous (fig. 1, 6), in lateral view (fig. 33, 34) shows a slightly down curvature; dorsal lump salient, in profile (fig. 1-6)................. 2 + + +- In dorsal view, inner distal margin of right mandible not continuous, but twisted inward and downward (figs. 7–15), in lateral view (fig. 35, 36) internal margin, almost straight, the tip abruptly downward curving; dorsal lump slightly salient, in profile (fig. 7–15) ......................................................................................................... 7 + + + + + +2. Ocelar spots present as a slight elevation in the dorsal surface of the head (fig. 3, arrow) ............... + + +O +. wheeleri + + + + + +- Ocellar spots absent (figs. 1, 2, 4–6)....................................................................................................................3 + + + + + +3. Labrum single lobed, head capsule with only scattered bristles (fig. 5) ................................. + + +O +. mirim + + + +sp. nov. + + + + +- Labrum with middle lobe distinct........................................................................................................................4 + + + + + +4. Head capsule covered with a continuous mat of short hairs (fig. 6) ........................................ + + +O +. pilosus + + +sp. nov + + + +- Head with scattered bristles and/or short hairs.................................................................................................... 5 + + + + + +5. Flanges with a light constriction on the base (fig. 4) + +...................................................... + +O +. tubesauassu + + + +sp. nov. + + + + +- Flanges without a constricted base (figs. 1, 2); known only from Amazonian forest (fig. 30, stars and filled squares)..............................................................................................................................................................................6 + + + + + +6. Head capsule length always larger than 2.90 mm (fig. 1) ................................................................... + + +O +. humilis + + + + + + +- Head capsule length always shorter than 2.80 mm (fig. 2) + +............................................................... + +O +. aduncus + + + + + + + + +7. Head capsule full covered with a mat of short hairs, without bristles (fig. 10) + +............................ + +O +. gibberorum + + + + + +- Head capsule without a mat of short hairs on entire surface (figs. 7–9, 11–15)..................................................8 + + + + + +8. Tip of the left mandible strongly hooked, curved backward; tip of the right mandible twisted forming a 90º angle with proximal portion of mandible (fig. 11) + +................................................. + +O +. uncimandibularis + + + +sp. nov. + + + + +- Tip of the left mandible lightly curved, not backward as above; tip of the right mandible twisted, always form- ing a larger than angle 90º (fig. 7–9, 12–15).......................................................................................................9 + + + + +9. Head with parallel and straight sides (figs. 12, 13, 15)......................................................................................10 + + +- Head with parallel sides, irregular sides (fig. 14) or slightly convergent in front, always somewhat convex (figs. 7–9)..........................................................................................................................................................12 + + + + + +10. Width of head about 70 % of head length or more + +................................................................... + +O +. macrocephalus + + + + + +- Width of head lesser than 70 % of head length.................................................................................................. 11 + + + + + +11. Length of head capsule shorter than 3.2 mm; ventral surface of head capsule densely covered of short hairs and some bristles (fig. 13)............................................................................................................. + + +O +. okeyma + + + +sp. nov. + + + + + +- Length of head capsule larger than 3.2 mm; ventral surface of head capsule with scattered bristles and without short hairs (fig. 12) + +..................................................................................................................... + +O +. orthognathus + + + + + + + +12. Mandible length shorter than head capsule (near 80% of its length); head capsule length longer than 3.28 mm (figs. 7, 8) .......................................................................................................................................................... 13 + + +- Mandible length almost equal to the head capsule; head capsule length shorter than 3.00 mm (figs. 9, 14) .. 14 + + + + + +13. Head with parallel and convex sides (fig. 8) ......................................................................................... + + +O +. heberi + + + + + + +- Head with sides slightly converging in front (fig. 7) .......................................................................... + + +O +. insignis + + + + + + + + +14. Head with irregular sides (fig. 14) .................................................................................. + + +O +. longilamina + + + +sp. nov. + + + + + +- Head with regular and convex sides (fig. 9) + +.................................................................................. + +O +. brevipilosus + + + + + + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFDA745DFF27F98DFDD649BF.xml b/data/38/3D/C5/383DC579FFDA745DFF27F98DFDD649BF.xml new file mode 100644 index 00000000000..fac1beffdcc --- /dev/null +++ b/data/38/3D/C5/383DC579FFDA745DFF27F98DFDD649BF.xml @@ -0,0 +1,155 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes humilis +Constantino + + + + +(figs. 1, 27, 30) + + + + + +Orthognathotermes humilis + +Constantino, 1991 +:200 + + +; (Imago and worker, 28–30). + + + + + +Holotype +: +MPEG +(soldier), not examined. + + +Paratypes +: soldiers and workers. +BRAZIL +. +Amazonas +:, Maraã (Rio Japurá): +11.x.1988 +, Reginaldo Constantino coll. (9249); Maraã (Rio Japurá): +11.x.1988 +Reginaldo Constantino coll. (MPEG-2825). All examined. + +Imago. Unknown. +Soldier. Head with sides slightly convergent in front in dorsal view. In profile dorsal lump salient behind the flanges. Mandibles of the first pattern, tooth-like projection at proximal half. Head capsule with sparse short hairs and bristles, short hairs denser on ventral surface, scattered microscopic hairs on surface, denser in distal portion. Posmentum with short hairs. Pronotum with short hairs on the surface and bristles on posterior and anterior margins, mesonotum and metanotum with short hairs and bristles in posterior margins, abdominal tergites denser covered with short hairs and few bristles on margins; sternites with short hairs on surface and bristles on posterior margins. + +Comparisons. + + +O +. humilis + + +soldier has a head capsule larger than all other species of the same mandible pattern. The most similar species are + + +O + +. +wheeleri + +, in which soldier has ocellar spots and different mandibles (shorter from marginal tooth-like projection to the tip), + + +O +. aduncus + + +is smaller and + + +O + +. +tubesauassu + + +sp. nov. + +with smaller flanges slightly constricted at bases. + + + + +Geographical distribution. +All records of + + +O +. humilis + + +are in Amazonian forest ( +Fig. 30 +), except Humaitá, a savanna formation inside the forest. + + + + +Material examined. +BRAZIL +. +Amazonas +: Humaitá: +17.i.1990 +, R. Constantino coll. (9422); Manaus: +4– 5.xii.1990 +, F.B Apolinário coll. (9472). + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFDB7452FF27FA62FB374ECB.xml b/data/38/3D/C5/383DC579FFDB7452FF27FA62FB374ECB.xml new file mode 100644 index 00000000000..c39535351e4 --- /dev/null +++ b/data/38/3D/C5/383DC579FFDB7452FF27FA62FB374ECB.xml @@ -0,0 +1,295 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes heberi +Raw & Egler + + + + +(figs. 8, 21, 29) + + + + + +Orthognathotermes heberi + +Raw & Egler, 1985 +:333 + + +(soldier, table 1). + + + + + +Holotype +: lost. See comments below. + + +Neotype +, here designated: soldier: MZUSP-9078, +Brazil +, Goiás, Parque Nacional das Emas, +24.IX.1982 +, A. Raw coll., kept separately in the same vial with the +paratypes +, part of the same lot as the +holotype +. + + +Paratypes +: soldiers and workers. +BRAZIL +. +Goiás +: Parque Nacional das Emas: +24.IX.1982 +, A. Raw coll. (9078). Examined. + +Imago. Eyes small, distant from the inferior margin of head by less than the larger diameter of the ocellus. Ocelli reniform in dorsal view, oval, remote from the eye by distance equal to its minimum diameter in lateral view. Fontanelle broad and medium-sized. Head capsule with few short hairs and bristles. Labrum with bristles not organized in rows. Pronotum densely covered with bristles. Mesonotum and metanotum with few bristles, concentrated in the center and posterior margins. Head sepia brown to pale brown, pronotum and tergites pale brown, sternites yellow, legs and wing scales pale brown. + +Comparisons. +The imago of + + +O +. heberi + + +differs from those of the other species by the combination of small ocelli and eyes and a large fontanelle. The most similar species is + + +O +. insignis + + +, from which it differs by the labrum with dispersed bristles and oval ocelli, distant from the eyes, and + + +O +. longilamina + + + +sp. nov. + +from which it differs by the ocelli less salient. + +Soldier. Head sides parallel in dorsal view. In profile dorsal lump slightly salient behind the flanges. Mandibles of the second pattern, tooth-like projection at proximal half. Head capsule with sparse bristles and short hairs denser in ventral surface, scattered microscopic hairs on surface denser on posterior margin. Posmentum with bristles. Pronotum with short hairs on the surface and bristles on margins, mesonotum and metanotum with bristles and short hairs on posterior margins, abdominal tergites covered with short hairs and bristles, sternites with bristles, longer on posterior margins. + +Comparisons. + + +O +. heberi + + +soldier is larger than + + +O +. brevipilosus + +, + +O +. longilamina + + + +sp. nov. + +, + + +O +. macrocephalus + +, + +O +. okeyma + + + +sp. nov. + +and has parallel head capsule sides (slightly convergent in front in + + +O +. insignis + + +and + + +O +. uncimandibularis + + + +sp. nov. + +, both most similar species). + + + + +Geographical distribution. +All records of + + +O +. heberi + + +are in open formations, like pastures and cerrados ( +Fig. 29 +), the record from Manaus, Amazonas State, is in a pasture that opens inside the forest. + + +Evidence that the +holotype +was lost: Anthony Raw personally confirmed that the vial containing the +holotype +was lost and was never deposited in the collection of the University of +Brasília + + + + +Comments. +In the original description the authors mention some institutions as depositories of +paratypes +, however only in MZUSP do we confirm the presence of the material. + + +The minor soldiers described by +Raw & Egler (1985) +are individuals infested by a undetermined species of Acanthocephala. The soldier caste is monomorphic, contrary to the original description. + + + + +Material examined. +BRAZIL +. +Amazonas +: Manaus: +21.v.1977 +, A.Bandeira coll. (8321). +Distrito Federal +: +Brasília +: +16.vii.1971 +, Kiniti Kitayama coll., (5415*); 1970 (6998); Fazenda Água Limpa: +29.vi.1980 +, A. E. Mill coll. (MPEG-1307); 1993, K. Kitayama coll. (UnB-1110, UnB-1111); +17, 19 and 21.xi. +1992, Marcelo Lima coll. (UnB-1115, UnB-1118, UnB-2112*, UnB-1127); 14,15, and +21.xi.1992 +, Carlos coll. (UnB-1116, UnB-1117, UnB-1121, UnB-1124, UnB-1125); Planaltina– +CPAC +: +16.iv.1998 +, V.S. Dias coll. (UnB-942, UnB- 944, UnB-945, UnB-946); Reserva Biológica Águas Emendadas: +10.x.1986 +, R. Constantino coll. (MPEG- 2635); +20.x.1986 +, (MPEG-2672*); Reserva Ecológica do +IBGE +: +18.ix.1998 +, R. Constantino coll. (UnB-1282, UnB-1293*). +Goiás +: Parque Nacional das Emas: +9.vii.1980 +, A. Mill & K. Redford coll. (MPEG-1203*); +28.iii-6.iv.1984 +, Exp. MZ-IQUSP coll. (8426); +15.i.1986 +. (9288); +2.v.1980 +, K.H. Redford coll. (10112*); +25.vii.1983 +, D. Brandão coll. (UFG-77, UFG-84, UFG-86); +17.i.2004 +, D.A. Costa coll. (12118); +26.x.2001 +, R. Constantino coll. (UnB-3016, UnB-3059*, UnB-3061). +Minas Gerais +: Fazenda Rossato: 27,28. +x.2001 +, R. Constantino coll. (UnB-3082, UnB-3131); Guanhães: +2.iii.1972 +, R.L. Araujo coll. (5059, 5102, 5124*); Paracatu: +14.ii.1972 +, K. Kitayama coll. (7366, 7367); São Gotardo: +vi.1986 +, Gilberto F. Corrêa coll. (8850); Uberaba/Uberlândia: +9.xi.1972 +, R.L. Araujo coll. (5700). +Mato Grosso do Sul +: +Costa Rica +: +ii.1986 +, +IQUSP +coll. (8782). +Mato Grosso +: Chapada do Guimarães: +11.xi.1982 +,? coll. (MPEG-2764). + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFDB7453FF27FEF9FA8B4E6A.xml b/data/38/3D/C5/383DC579FFDB7453FF27FEF9FA8B4E6A.xml new file mode 100644 index 00000000000..3c60b936804 --- /dev/null +++ b/data/38/3D/C5/383DC579FFDB7453FF27FEF9FA8B4E6A.xml @@ -0,0 +1,197 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + + +Orthognathotermes gibberorum +Mathews + + + + +(figs. 10, 32) + + + + + +Orthognathotermes gibberorum + +Mathews, 1977 +:126 + + +(soldier, 75). + + + + + +Holotype +: +MZUSP +(soldier: MZUSP-7411, +12 +º 49´S +51º 46´W +, Serra do Roncador, Mato Grosso, +Brazil +, A.G.A Mathews coll., kept separately in the same vial of +paratypes +), examined. See comments below. + + +Paratypes +: soldiers and workers. +BRAZIL +. +Mato Grosso +: +12º 49´S +51º 46´W +, Serra do Roncador: A.G.A Mathews coll. (7411). Examined. + +Imago. Unknown. +Soldier. Head sides parallel in dorsal view. In profile, dorsal lump slightly salient behind the flanges. Mandibles of the second pattern, with tooth-like projection at half. Head capsule covered with dense mat of short hairs on surface. Posmentum with bristles and sparse short hairs. Pronotum with bristles on anterior and posterior margins, scattered short hairs on the surface, mesonotum and metanotum with bristles in posterior margins, abdominal tergites and sternites densely covered with bristles, with some erect bristles on posterior margins. + +Comparisons. + + +O +. gibberorum + + +soldier differs from all other species (of the same mandibles pattern) by a denser layer of short hairs on entire head capsule. + + + + +Geographical distribution. +The +type +locality of + + +O +. gibberorum + + +is in the transition between Cerrado and the Amazonian forest, in the “Serra do Roncador” ( +Constantino & Cancello, 1992 +). Mathews collected the +holotype +in a nest of + +Cornitermes snyderi + +in an open formation (Campo/Cerrado margin). The new record of this species is in a Cerrado formation. + + + + +Comments. +The +types +labels do not have a collecting date. +Mathews (1977) +mentioned that all the material was collected by him during the Royal Geographic Expedition, between: +ix.1967 +and +x.1968 +. + + +The + + +O +. gibberorum + + +soldier is very close to + + +O +. heberi + + +. The prominence above the head forming two lumps may vary among individuals of the same colony; it may be present in other species ( + + +O +. heberi + + +, + + +O +. insignis + + +, + + +O +. uncimandibularis + + + +sp. nov. + +), and there is variation among individuals of the same sample. + + + + +Material examined. +BRAZIL +. +Amapá +: Aporema: +26.x.1989 +, R. Constantino coll. (MPEG-3227). + + + + \ No newline at end of file diff --git a/data/38/3D/C5/383DC579FFDC7456FF27F8DAFEAE4C56.xml b/data/38/3D/C5/383DC579FFDC7456FF27F8DAFEAE4C56.xml new file mode 100644 index 00000000000..0d08ac1fd89 --- /dev/null +++ b/data/38/3D/C5/383DC579FFDC7456FF27F8DAFEAE4C56.xml @@ -0,0 +1,255 @@ + + + +Revision of the Neotropical termite genus Orthognathotermes Holmgren (Isoptera: Termitidae: Termitinae) + + + +Author + +Rocha, Mauricio Martins Da + + + +Author + +Cancello, Eliana M. + +text + + +Zootaxa + + +2009 + +2280 + + +1 +26 + + + +journal article +10.5281/zenodo.191174 +474ca204-aff4-4716-85d5-cace137e3e78 +1175-5326 +191174 + + + + + + +Genus + +Orthognathotermes +Holmgren, 1910 + + + + + + + + + +Orthognathotermes + +Holmgren, 1910 +:286 + + +. + + + + + +Orthognathotermes + +; + +Mathews, 1977 +:124 + +(redescription). + + + + + +Type +species: + +Mirotermes macrocephalus +Holmgren, 1906 + +, by original designation. + + + + +Etymology: +From the Greek “ +orthos +” (rectilinear) + “ +gnathos +” (mandibles), and the Latin “ + +termes + +” (termite), in reference to soldier’s straight and elongated mandibles. + + +Imago. Head rounded in dorsal view, fontanelle at the level of posterior half of eyes, broad (fig. 16) or narrow (fig. 18), and large (fig. 20), medium (fig. 17), or small (fig. 18). Eyes large (fig. 18) or small (fig. 19), in profile, distant from the inferior margin of head by a distance equal or less than the larger diameter of the ocellus. Ocelli in dorsal view semicircular (fig. 16), reniform and narrowed (fig. 19), or reniform and large (fig. 18), in lateral view oval (fig. 16) or sub-triangular (fig. 20). Ocellus remote from the eye by distance equal to its minimum diameter (fig. 19), or less (fig. 17), or touching the eye (fig. 16). Postclypeus convex in lateral view, elevated above dorsal margin of head (fig. 16). Antennae with 17 articles: second half of first, third half of second, fourth one third larger than third, fifth one third larger than fourth, sixth through eighth enlarge successively, the others subequal (except in + + +O +. heberi + + +: fourth through eighth enlarge successively, the others subequal; in + + +O +. aduncus + + +and + + +O +. mirim + + +, third and fourth half of second, fifth one third larger than fourth, sixth through eighth enlarge successively, the others subequal). Mandibles similar to those of the workers. Pronotum semicircular (fig. 23) to sub trapezoidal (fig. 19), anterior margin slightly concave and posterior emarginated, posterior margin of mesonotum and metanotum emarginated. Tibial spurs formula 3:2:2. Wings approximately twice the length of body. Head covered with scattered bristles and a mat of short hairs, varying in density in each species; labrum with 12 bristles in two rows (fig. 16) or not organized in rows (fig. 17). Antennae covered with short hairs and bristles. Pronotum covered with bristles and short hairs varying in density according each species. Abdominal tergites and sternites densely covered with bristles and short hairs, and with a row of bristles on the posterior margin. Legs covered with bristles and short hairs, with spines in the internal margins of tibiae. Wing scales covered with bristles, and the surface of wings with short hairs. Head capsule with three pale spots - two in front of the ocelli and one above the fontanelle - wing veins brown, wing cells pale brown and translucent. + + +Soldier. Head capsule sub rectangular in dorsal view, with sides parallel (fig. 2) or slightly convergent in front (fig. 7); posterior margin with or without longitudinal furrow (fig. 8); distinct prominence or lump (fig. 2, see arrow) in profile, less (fig. 15) or more salient (fig. 2); a flange near each antennal socket (fig. 1, arrow). Frontal pore and frontal gland indistinct. Mandibles curving downward in profile (fig. 1), very long and narrow, with a tooth-like projection near middle (fig. 6) or at proximal half (fig. 1), tips hooked inward, strongly hooked in the left mandible of + + +O +. uncimandibularis + + + +sp. nov. + +(fig. 11), lightly hooked in the other species; two basal teeth on left mandible and one on the right, sharp cutting edge on inner margin extends from the tooth-like projection to near tip, blades elbowed outwards at the same point level; circular section at the proximal part. Labrum with middle lobe distinct (fig. 1), except in + + +O +. mirim + + +(without lobes, fig. 5 and + + +O +. brevipilosus + + +, weakly trilobated,fig. 9). Ocellar spots appear only in + + +O +. wheeleri + + +(fig. 3 arrow). Antennae with 15 articles: first longest, second half of first, third half of second, fourth and fifth equal to second, sixth one third longer than fifth, the others subequal and one third longer than sixth (except in + + +O +. okeyma + + +and + + +O +. orthognathus + + +: fourth and fifth one third longer than second, and sixth equal to second). Postmentum elongate, with concave lateral margins. Pronotum with anterior and posterior trapezoidal lobes, with emarginated margins, both lobes forming a close angle in profile. Tibial spurs formula 3:2:2. Pilosity of head variable in each species. Antennae covered with short hairs and bristles. Labrum: with variable number of bristles, forward oriented in median lobe, sparse and erect in the rest of the surface. Body covered with bristles and short hairs, variable according to species. Postmentum with two clusters of two to five bristles near the anterior margin, and short hairs and bristles scattered on the rest of the surface. Legs with scattered short hairs and bristles plus some spines on the internal margins of tibiae. Head orange in majority of individuals, but may vary from brown to yellow, mandibles ferruginous to black, body pale-yellow. + + +Worker. Morphologically uniform among species. Head rounded, +Y +suture invisible. Antennae with 15 articles, or if 14, the third subdivided. Anteclypeus, postclypeus and labrum similar in shape to those of imago. Pronotum with anterior lobe slightly larger than posterior, with an angle near 90º between them, anterior lobe slightly emarginate. Mandibles described below. Tibial spurs formula: 2:2:2. Fontanelle rounded and visible. Entire head covered with scattered bristles and very few short hairs. Pronotum with bristles and short hairs concentrated in anterior and posterior margins, mesonotum and metanotum with bristles and short hairs on posterior margins, abdominal tergites and sternites densely covered with short hairs and bristles, both with a row of erect bristles on posterior margins. Legs covered with scattered bristles and short hairs. + +Worker/Imago mandibles (fig. 25). Left mandible: apical tooth twice the size of M1+2, an acute angle between apical and M1+2, a sinuous blade between M1+2 and M3, M3 much smaller than M1+2 and equidistant from the anterior point of M1+2 and the molar prominence, molar tooth conspicuous, molar prominence without ridges and very concave. Right mandible: apical tooth with more than twice the size of M1, M2 much smaller than M1, molar plate without ridges and very concave. +Digestive tube (fig. 24). Foregut: crop developed, without any constriction between it and the gizzard, cuticular armature of the gizzard complete with 24 visible folds, six of first order, six of second and 12 of third (fig. 28 A). Midgut: mixed segment with a long mesenteric tongue dorsally placed in right lateral view of the tube in situ (fig. 24 B). Two pairs of Malpighian tubules, each tubule with a distinct insertion on the junction mesenteron-proctodeum, on the opposite side of the mesenteric tongue of the mixed segment (fig. 28 B). Hindgut: P1 long, in ventral view, forming an arch from the left side of body through the right, circling P3 (fig. 24 C), going to the right side until the P2 and its insertion in P3 (fig. 24 B). This insertion is not visible as it is covered by P4 (fig. 24 B). P3 large, without any visible ornamentation at 400x magnification, P3a voluminous, P3b funneled, P4 long. +Enteric valve (figs. 26, 27): armature composed of six cushions of three kinds: three fully-developed cushions (dark large arrow), two medium-sized, with fewer spines (light arrow), and one reduced, with much fewer and smaller spines (dark tiny arrow). The largest three cushions are intercalated with the others, bearing finger-like projections covered with a few spines on the internal face, extending into the lumen of P3. That largest plate with bulbous base is on the opposite side of the most reduced plate. + + + +Comments: +the differences in figures are due to positioning of the parts in the slides. + + + + +Biology. + +Orthognathotermes + +is endemic to the Neotropical region, occurring in different vegetation zones, including the Brazilian Cerrado and dense tropical forests. + + +Information on the biology of + +Orthognathotermes + +species is rare, sparse, and some comes from field notes of collectors, as for instance, on the nest of + + +O +. heberi + + +. This species may live in nests constructed by other species or build its own nests, that are low mounds, built with soft earth, and frequently extend several centimeters underground (Coles de +Negret & Redford, 1982 +). +Araujo (1977) +describe a similar nest for + + +O +. insignis + + +. + + +They probably feed on humus in subterranean galleries ( +Mathews, 1977 +, Coles de +Negret & Redford, 1982 +). The morphology of the workers mandibles (humivorous +type +) and the detection of sand particles in the gut are in agreement with this hypothesis. + + +Soldiers of + +Orthognathotermes + +have two +types +of defense mechanisms ( +Mill, 1982 +): mechanical, by snapping/slashing mandibles and chemical, by viscous substance produced by the salivary glands and released in opponents by rupturing of the body wall and oral cavity. +Mill (1984) +reported that soldiers are capable of autolysis, breaking the body wall between the coxae and releasing a substance that becomes viscous in contact with air. +Mathews (1977) +mentioned that gland products are expelled through the mouth. We found a few soldiers with signs of rupture on their bodies, but some specimens exhibited a hardened secretion covering all pre-oral cavities and mandibles. It is not known which gland is responsible for the secretion; +Mill (1984) +stated that it is a salivary gland product, while +Mathews (1977) +mentioned at first that the secretion is a salivary gland product (p. 65–66), and in the genus redescription, that it is a frontal gland product (p. 128). We were not able affirm which species was examined by Mill in both papers, as only part of his material is housed in MZUSP. + + + + \ No newline at end of file diff --git a/data/38/3E/1F/383E1F9D3801C7570CBF3A277F213FB7.xml b/data/38/3E/1F/383E1F9D3801C7570CBF3A277F213FB7.xml new file mode 100644 index 00000000000..4a684b73ef1 --- /dev/null +++ b/data/38/3E/1F/383E1F9D3801C7570CBF3A277F213FB7.xml @@ -0,0 +1,196 @@ + + + +Flora Helvetica - Asteraceae + + + +Author + +Konrad Lauber + + + +Author + +Gerhart Wagner + + + +Author + +Andreas Gygax + +text + + +2018 +Haupt Verlag + +Bern + + + +Flora Helvetica + + + +1074 +1250 + + + +book chapter +978-3-258-08047-5 + + + + + +Filago gallica +L. + + + + + +Artbeschreibung: +10-20 cm +hoch, gabelig verzweigt, + +graufilzig. +Blaetter +schmal-lineal + +, die +groesseren +nur +1-2 cm +lang und kaum +1 mm +breit, mit pfriemlicher Spitze. + +Bluetenkoepfchen +zu 2-6 +knaeuelig +gehaeuft +, von den obersten +Staengelblaettern +weit +ueberragt + +(nur bei dieser +F. +-Art). +Huellblaetter +meist 15-20, +/- stumpf, zur Fruchtzeit ausgebreitet, die mittleren mit +verhaerteter +, +kahnfoermiger +Aussackung. + + + + +Bluetezeit +: 7-9 + + +Standort und Verbreitung in der Schweiz: Sandige +Aecker +, Brachfelder / kollin / +Frueher +besonders MW und JN + + + + +Verbreitung global: +Westeuropaeisch-mediterran + + + + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl Fsehr trockenLichtzahl LhellSalzzeichen1
Reaktionszahl Rsauer (pH 3.5-6.5)Temperaturzahl T +sehr warm-kollin (nur an +waermsten +Stellen, Hauptverbreitung in +Suedeuropa +) +
+Naehrstoffzahl +N + +maessig +naehrstoffarm +bis +maessig +naehrstoffreich + +Kontinentalitaetszahl +K +subozeanisch (hohe Luftfeuchtigkeit, geringe Temperaturschwankungen, eher milde Winter)
+
+
+ + +Volksname Deutscher Name: + +Franzoesisches +Filzkraut + +, + +Franzoesisches +Fadenkraut + +Nom +francais +: + +Cotonniere +de France + +Nome italiano: +Bambagia francese + + +
+
\ No newline at end of file diff --git a/data/38/3E/EF/383EEFFFC9E25EA4A2CEC9F527CC0590.xml b/data/38/3E/EF/383EEFFFC9E25EA4A2CEC9F527CC0590.xml new file mode 100644 index 00000000000..a30106f8c8e --- /dev/null +++ b/data/38/3E/EF/383EEFFFC9E25EA4A2CEC9F527CC0590.xml @@ -0,0 +1,716 @@ + + + +Revision of the genera Eutrecha and Xenotrecha (Solifugae: Ammotrechidae), taxonomic notes on Ammotrechinae, and description of a remarkable new Eutrecha from Colombia + + + +Author + +Botero-Trujillo, Ricardo +https://orcid.org/0000-0002-6199-6572 +Division of Invertebrate Zoology, American Museum of Natural History, Central Park West at 79 th Street, New York, NY 10024 - 5192, USA & Division Aracnologia, Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " - CONICET, Avenida Angel Gallardo 470, CP: 1405 DJR, C. A. B. A., Buenos Aires, Argentina + + + +Author + +Martinez, Leonel +Division Aracnologia, Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " - CONICET, Avenida Angel Gallardo 470, CP: 1405 DJR, C. A. B. A., Buenos Aires, Argentina + + + +Author + +Iuri, Hernan Augusto +Division Aracnologia, Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " - CONICET, Avenida Angel Gallardo 470, CP: 1405 DJR, C. A. B. A., Buenos Aires, Argentina + + + +Author + +Ojanguren-Affilastro, Andres Alejandro +Division Aracnologia, Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " - CONICET, Avenida Angel Gallardo 470, CP: 1405 DJR, C. A. B. A., Buenos Aires, Argentina + + + +Author + +Carvalho, Leonardo Sousa +https://orcid.org/0000-0003-4700-5610 +Universidade Federal do Piaui, Campus Amilcar Ferreira Sobral, BR 343, km 3.5, Bairro Meladao, s / no. CEP 64800 - 000, Floriano, PI, Brazil +carvalho@ufpi.edu.br + +text + + +Arthropod Systematics & amp; Phylogeny + + +2023 + +2023-04-04 + + +81 + + +317 +344 + + + + +http://dx.doi.org/10.3897/asp.81.e95181 + +journal article +http://dx.doi.org/10.3897/asp.81.e95181 +1864-8312-81-317 +BE57FF40714740AC8BEA1706A95DA4ED +C3B28C3FAD9250BC906A4A865EAA18B4 + + + + +3.1.3. +Eutrecha belenensis +sp. nov. + + + + +Figs 1 +, 2C +, 4 +, 5 +, 6 + + + +Material examined. + + + +Holotype +. +COLOMBIA + +• +1 ♂ +; + +Norte de Santander + +, + +Playa de +Belen + +, + +Area + +protegida +Los Estoraques +, +Centro Administrativo +; +08°13′15.3″N +73°14′18.25″W +; + +1400 m + +.a.s.l.; +17 Dec. 2015 +; +E. Henao +leg.; ICN +Aso +008. + + + + +Etymology. + +Latinized gentilicium that identifies this species as an inhabitant of Playa de +Belen +. + + + +Diagnosis. + +The male of + +Eutrecha belenensis + +features a series of morphological characteristics, each unique to this species among known species of + +Eutrecha + +, which allow to readily separate it from its congeners and provides a robust delimitation of the species on morphological grounds. These are: +i) +Cheliceral fixed finger with FM and FD teeth reduced in size (e.g., smaller than MSM, which is of normal size for a secondary tooth), yet both teeth evident (Figs +2C +, +5B +, +6 +). +ii) +Ventral margin of fixed finger asetose area (i.e., where distal teeth are situated) predominantly linear in lateral aspect (Figs +2C +, +5B +). +iii) +Movable finger of male moderately robust (e.g., relative to height of MP tooth) (Figs +2C +, +5D +). +iv) +MM tooth moderately smaller than MP, larger than MSM (Figs +2C +, +5B, D +, +6B +). +v) +MM tooth adjacent to MSM (Figs +2C +, +5B, D +). +vi) +Fixed finger mucron length more than twice height at its base; movable finger mucron length at least three times height at its base (Figs +2C +, +5B, D +). +vii) +Stridulatory apparatus consisting of a single set of ridges, all subparallel to the manus ventral surface (Fig. +5C, D +). +viii) +Flagellum narrowing distally in prolateral aspect, apex entire (non-bifid) (Figs +5C, D +, +6 +). +ix) +Attachment point of the flagellum subcircular (Fig. +5D +). +x) +Pedipalp tibia and basitarsus with ventral rows of about seven to nine spiniform setae each (Fig. +4B, C +). +xi) +Basitarsi of walking legs II and III, each with three proventral and two retrolateral spiniform setae (in addition to others on retroventral and retrodorsal series). +xii) +Basitarsus of leg IV with two distal retroventral spiniform setae (in addition to others on proventral series). +xiii) +Opisthosoma of male, ctenidia arranged into a single large area on 1st post-genital sternite (spiracular sternite I) (Fig. +4D +). + + + +Figure 4. + +Eutrecha belenensis + +sp. nov. +, holotype ♂ (ICN Aso 008), habitus, dorsal aspect ( +A +), sinistral pedipalp basitarsus and telotarsus, prolateral ( +B +) and ventral ( +C +) aspects, anterior opisthosomal sternites, with spiracular sternites centered ( +D +). Scale bars = 2 mm (A, D), 1 mm (B, C). Arrows: spiniform setae (in B and C); ctenidia on 1st post-genital sternite (in D). + + + + +Figure 5. + +Eutrecha belenensis + +sp. nov. +, holotype ♂ (ICN Aso 008), dextral chelicera, retrolateral aspect ( +A +) and close-up of fingers ( +B +), prolateral aspect ( +C +) and close-up of fingers and stridulatory plate ( +D +). Scale bars = 1 mm. + + + + +Figure 6. + +Eutrecha belenensis + +sp. nov. +, holotype ♂ (ICN Aso 008), dextral chelicera, fixed finger, ventral aspect ( +A +), schematic representation of fixed and movable fingers dentition, proventral aspect ( +B +). Scale bars = 0.5 mm. Abbreviations: FD, fixed finger, distal tooth; FM, fixed finger, medial tooth; FMAD, fixed finger, median apical diastema; FP, fixed finger, proximal tooth; FSM, fixed finger, submedial tooth; FT, fixed finger, terminal tooth; MM, movable finger, medial tooth; MN, movable finger, medial notch; MP, movable finger, proximal tooth; MPL, movable finger, prolateral tooth; MSM, movable finger, submedial tooth; MT, movable finger, terminal tooth; PFM, profondal medial tooth; PFP, profondal proximal tooth; PFSM, profondal submedial tooth; PFSP, profondal subproximal tooth; RFA, retrofondal apical tooth; RFM, retrofondal medial tooth; RFP, retrofondal proximal tooth; RFSP, retrofondal subproximal tooth. + + + + +Description of male. + +Based on holotype (ICN Aso 008). - +Measurements. +Linear measurements in Table +1 +. - +Color. +In 80% ethanol-preserved specimen. Prosomal dorsal shields and opisthosomal tergites with overall brown coloration (Fig. +4A +). Propeltidium with abundant dark brown areas, several paler spots distributed unevenly, and a median longitudinal pale brown line; ocular tubercle blackish. Meso-, metapeltidium, and opisthosomal tergites predominantly light brown, with small dark spots. Chelicerae, base color pale brown (same as pale propeltidial areas) (Fig. +5A, B +), with three dark brown longitudinal stripes on prodorsal, dorsal, and retrolateral surfaces of manus, which are interconnected distally by a broad, transverse stripe and posteriorly by a narrow, weakly defined stripe; stridulatory plate immaculately yellow (Fig. +5C, D +), with a proventral proximal brown spot. Asetose area of fixed and movable fingers reddish, with all teeth darkened (Fig. +5B, D +); movable finger setose area with ventral, brown-spotted area. Coxosternal region, opisthosomal sternites (Fig. +4D +), pleural membranes, trochanters of legs and pedipalps (Fig. +4A +), basifemora and telofemora of legs II-IV, and femur of leg I immaculately yellowish white; malleoli white. Pedipalp femur, tibia, and basitarsus dark brown (Fig. +4A, B +), with faint paler areas; telotarsus yellowish (Fig. +4B, C +). Legs with patella, tibia, basitarsus, and telotarsus brownish (Fig. +4A +), with coloration pattern similar to that of pedipalps but paler. - +Prosoma. +Propeltidium wider than long (Table +1 +); central region covered with short, spicule-like stout setae which become longer towards the outer borders (Fig. +4A +); the longer of these setae fall off and break easily, unlike the shorter ones; all setae seem to be apically worn. Ocular tubercle slightly elevated, with abundant macrosetae. Anterolateral propeltidial lobes separated from the propeltidium principal shield by incomplete lateral groove. Eyespots elongated. Meso- and metapeltidium wider than long, with abundant long macrosetae (Fig. +4A +). Coxae densely covered with abundant thin setae. Sternum glabrous. - +Chelicera-dentition and processes. +Fixed finger with median teeth series comprising well-developed FP tooth, whereas other primary teeth (FM and FD), as well as the FSM tooth, are small (Figs +2C +, +5B +, +6 +); FSD tooth absent; FM and FD teeth, each importantly displaced distally in the finger relative to the contiguous, more proximal tooth (FSM and FM, respectively), such that a medial notch (MN) and a median apical diastema (FMAD) are present; retrofondal teeth series uninterrupted (i.e., without FRFD), with four teeth (RFSP, RFP, RFM, RFA) (Fig. +6 +); basal retrofondal margin heavily sclerotized (Fig. +6A +); profondal teeth series consisting of four teeth (PFSP, PFP, PFSM, PFM) (Fig. +6B +). Fixed finger asetose area sinuous, with ventral margin predominantly linear in lateral aspect; prodorsal carina sharp, not elevated in lateral aspect, without angular dorsal crest; proventral carina weakly pronounced on the mucron area; fixed finger retrolateral carina (FRLC) absent. Fixed finger mucron without subterminal (FST) teeth; apex (FT tooth) curved, hook shaped. Movable finger with median teeth series comprising well-developed MP and MM primary teeth, the former of which is larger, and one MSM secondary tooth that is smaller than MM (i.e., MP> MM> MSM) (Figs +2C +, +5B +); MP, MSM, and MM close together; MP and MM each adjacent to MSM; MSM upright and triangular. Movable finger prolateral carina (MPLC) evident, ending slightly basal to MP in a small prolateral (MPL) tooth (Fig. +6B +). Movable finger without subproximal (MSP) or subterminal (MST) teeth; movable finger retroventral longitudinal carina (MRVC) present on distal half, or third, of finger, forming a smooth elevated ridge (Figs +2C +, +5B +); retrolateral longitudinal carina (MRLC) consisting of abundant conspicuous granules scattered on the retrolateral surface of finger. Movable finger mucron moderately long, with gnathal edge carina ordinary (not convex). Closure of RFA tooth basal to MP, of MM tooth distal to FM, when fingers are closed. - +Chelicera-setose areas and stridulatory plate. +Retrolateral and dorsal surfaces with abundant retrolateral manus ( +rlm +) and retrolateral finger ( +rlf +) setae, of different sizes, which are predominantly straight and rigid (Figs +4A +, +5 +); some of these setae are arranged in bilaterally symmetrical pattern, as are some principal retrolateral finger ( +principal rlf +) setae that are more flexible than others; movable finger retrolateral proximal setal cluster ( +rlpc +) dorsally with a single, long and markedly plumose seta. Prolateral surface with array of setal types (Fig. +5D +), as follows: proventral distal ( +pvd +) setae consisting of row of plumose setae, starting at level of the interdigital condyle ( +pic +) and ending near level of RFA tooth; proventral subdistal ( +pvsd +) setae arranged in rather disorganized pattern, +pvsd +comb not markedly differentiated; carpet-like field of bristle-like promedial ( +pm +) setae broad. Stridulatory plate longer than high, occupying most of the prolateral surface of manus (Fig. +5C, D +); stridulatory apparatus consisting of a single set of ridges, 6 or 7 in number, dorsalmost vestigial, all approximately parallel to the manus ventral surface. Distal limit of the prolateral setose area of movable finger reaching midpoint between MSM and MM teeth; movable finger prodorsal ( +mpd +) setal series consisting of plumose setae arranged in a rather staggered row, adjacent to abundant non-plumose setae of the movable finger promedial ( +mpm +) and proventral ( +mpv +) setal series. - +Chelicera-flagellum. +Of the composite type, without shaft. A thin, translucent, membranous structure immovably attached prodorsally to the fixed finger (Figs +5D +, +6 +); flagellar base general aspect bowl-shaped, long, and narrowing distally in prolateral aspect, nearly reaching the apex of the finger on its distal end; apex entire (non-bifid), bearing small spicules; attachment point subcircular, placed at the level of PFSM tooth. - +Pedipalp. +All segments coated with abundant short setae (Fig. +4A-C +); those on ventral surface of tibia, basitarsus, and telotarsus stouter and more distinct than those on other surfaces. Femur with spicule-like macrosetae; tibia with proventral and retroventral rows of eight spiniform setae each, which are short and stout; basitarsus with proventral and retroventral rows of seven to nine spiniform setae each (Fig. +4B, C +), stronger and longer than those on tibia; telotarsus without spiniform setae. Femur, tibia, basitarsus, and telotarsus with few long thin setae; clubbed setae apparently absent. Retroventral surface of femur proximally with a suture-like cleavage plane. Telotarsus with retrodorsal pore area on distal third. - +Leg I. +All segments coated with abundant short setae similar to those on pedipalps (Fig. +4A +), without stout or spiniform setae; tibia and basitarsus with few long thin setae. Telotarsus with apical retrodorsal pore area similar to that of pedipalp; without claws or spiniform setae. - +Walking legs. +Covered with abundant short and a few long setae, like those on pedipalps and legs I (Fig. +4A +). Legs II and III: basitarsus with seven or eight spiniform setae: three proventral (distal, subdistal, and sub-basal), one or rarely two retroventral (distal), two retrolateral (subdistal and basal), and one retrodorsal (distal); telotarsus bi-segmented (consisting of large basal and small distal segments), with proventral row of four to six spiniform setae (along basal and distal segments) and a retroventral row of three or four (along basal segment only), in 2.2.2/1, 2.2.2/1.1, or 2.2.2.2/1.1 pattern; in addition, the basal segment of sinistral leg II telotarsus bears two extra spiniform setae adjacent to the retrolateral series (not aligned with the row but in more submedial position). Leg IV: basitarsus with row of three/four proventral and two distal retroventral spiniform setae; telotarsus 3-segmented (the two segmentation lines are complete), with proventral and retroventral rows of four spiniform setae each (along basal and median segments only), in 2.2.2/2/0 pattern. - +Opisthosoma. +Tergites with abundant setae similar to those on propeltidium (Fig. +4A +); setation of the sternites comparable to that of coxae. Ctenidia present on 1st post-genital sternite (spiracular sternite I) (Fig. +4D +); ctenidia in the form of abundant, short +"fleshy" +setae, densely arranged into what looks like a single large area on the sternite; other sternites without ctenidia. + + + +Table 1. +Measurements (mm) for + +Eutrecha belenensis + +sp. nov. +, + +Eutrecha florezi + +Villareal-Blanco, Armas and +Martinez +, 2017, and + +Xenotrecha huebneri + +(Kraepelin, 1899). Material deposited in the +Colecao +de +Historia +Natural, Universidade Federal do +Piaui +(CHNUFPI), Floriano, Brazil; the Instituto de +Investigacion +de Recursos +Biologicos +"Alexander von Humboldt" (IAvH), Villa de Leyva, Colombia; the Arachnological Collection of the Instituto de Ciencias Naturales (ICN), Universidad Nacional de Colombia, +Bogota +; the Museo Javeriano de Historia Natural "Lorenzo Uribe, S.J.," Pontificia Universidad Javeriana (MPUJ), +Bogota +. 1 Excludes chelicerae. 2 Excludes claws. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Species + + +E. belenensis + + + +E. florezi + + + +X. huebneri + +
Type/sexHolotype ♂
CollectionICN Aso 008IAvH I 472MPUJ ENT 61895CHNUFPI 1247CHNUFPI 1248
Total body length19.9411.3112.4210.379.31
PropeltidiumLength2.063.133.143.032.9
Width2.2632.482.732.9
CheliceraLength3.523.53.953.273.33
Width1.011.31.111.331.5
Height1.041.171.221.21.33
Pedipalp total length12.8814.0314.3614.0410.56
FemurLength4.094.664.94.663.5
Width0.810.8710.970.73
Height0.690.970.871.070.83
TibiaLength4.434.984.984.723.53
Width0.640.730.870.730.6
Height0.590.770.760.770.57
Basitarsus + telotarsusLength4.364.394.484.663.53
Leg I total length8.037.68.136.975.84
PatellaLength2.382.332.512.171.83
TibiaLength2.832.672.92.432.07
BasitarsusLength1.761.61.711.51.17
TelotarsusLength1.0611.010.870.77
Leg IV total length14.0714.2513.7913.2411.06
PatellaLength4.64.794.434.323.56
Width0.680.970.990.830.73
Height1.021.41.441.331.1
TibiaLength4.684.664.84.393.73
Width0.460.620.570.60.52
BasitarsusLength3.173.33.173.32.77
Telotarsus2Length1.621.51.391.231
+
+
+ +Female. +Unknown. + + +Distribution. + + +Eutrecha belenensis + +is known only from the type locality in the department of Norte de Santander, Colombia (Fig. +1 +). + + +
+
\ No newline at end of file diff --git a/data/38/3F/18/383F18699DBDC4AED04A7E99E1408400.xml b/data/38/3F/18/383F18699DBDC4AED04A7E99E1408400.xml new file mode 100644 index 00000000000..83e4141f0c5 --- /dev/null +++ b/data/38/3F/18/383F18699DBDC4AED04A7E99E1408400.xml @@ -0,0 +1,71 @@ + + + +Cyanobacteria of Greece: an annotated checklist + + + +Author + +Gkelis, Spyros + + + +Author + +Ourailidis, Iordanis + + + +Author + +Panou, Manthos + + + +Author + +Pappas, Nikos + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +10084 +10084 + + + + +http://dx.doi.org/10.3897/BDJ.4.e10084 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e10084 +1314-2828--10084 + + + + +Mastigocladus laminosus Cohn ex Kirchner, 1898 + + + + +Mastigocladus laminosus + + + +Notes + +Anagnostidis 1961 + + + + \ No newline at end of file diff --git a/data/38/3F/51/383F51F2B111534A946D20F387483195.xml b/data/38/3F/51/383F51F2B111534A946D20F387483195.xml new file mode 100644 index 00000000000..49902b3e872 --- /dev/null +++ b/data/38/3F/51/383F51F2B111534A946D20F387483195.xml @@ -0,0 +1,92 @@ + + + +Taxonomic updates in Amphitecna (Bignoniaceae): A new Mexican species and the re-establishment of the giant-leaved A. megalophylla + + + +Author + +Gomez-Dominguez, Hector +Herbario Eizi Matuda (HEM) Instituto de Ciencias Biologicas, Universidad de Ciencias y Artes de Chiapas, Tuxtla Gutierrez, Chiapas, Mexico + + + +Author + +Ortiz-Rodriguez, Andres Ernesto +Departamento de Botanica, Instituto de Biologia, Universidad Nacional Autonoma de Mexico, Mexico +ortizrodriguez.ae@gmail.com + + + +Author + +Velasco-Espino, Delfilia +Herbario Eizi Matuda (HEM) Instituto de Ciencias Biologicas, Universidad de Ciencias y Artes de Chiapas, Tuxtla Gutierrez, Chiapas, Mexico + + + +Author + +Hernandez-Burguete, Rene +Herbario Eizi Matuda (HEM) Instituto de Ciencias Biologicas, Universidad de Ciencias y Artes de Chiapas, Tuxtla Gutierrez, Chiapas, Mexico + +text + + +PhytoKeys + + +2021 + +2021-01-25 + + +171 + + +75 +90 + + + + +http://dx.doi.org/10.3897/phytokeys.171.55397 + +journal article +http://dx.doi.org/10.3897/phytokeys.171.55397 +1314-2003-171-75 +B145490BD62B597DA238655B709B325A + + + + + +Amphitecna megalophylla (Donn. Sm.) A.H. Gentry + + + + +Neotuerckheimia megalophylla +Donn. Sm., Bot. Gaz. (Crawfordsville) 47: 258, f.l. 1909. Basionym. + + + +Distribution. +Guatemala (endemic). + + +Specimens examined. + +Guatemala. Alta Verapaz, Coban: 1350 m, + +Tuerckheim +H. von II 2278 + +(isosyntype, M). + + + + + \ No newline at end of file diff --git a/data/38/3F/79/383F792640A954AE96621BDEE77E3CD3.xml b/data/38/3F/79/383F792640A954AE96621BDEE77E3CD3.xml new file mode 100644 index 00000000000..a9dd353bc12 --- /dev/null +++ b/data/38/3F/79/383F792640A954AE96621BDEE77E3CD3.xml @@ -0,0 +1,92 @@ + + + +Diversity pattern of insects from Macao based on an updated species checklist after 25 years + + + +Author + +Xian, Chunlan +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China + + + +Author + +Leong, Chi Man +Department of Life Sciences, Faculty of Science and Technology, Beijing normal university - Hong Kong Baptist University United International College, Zhuhai, China & Macao Entomological Society, Estrada Coronel Nicolau de Mesquita, Macao SAR, China + + + +Author + +Luo, Jiuyang +https://orcid.org/0000-0002-2748-9534 +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China + + + +Author + +Jia, Fenglong +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China + + + +Author + +Han, Hongxiang +Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, China +hanhx@ioz.ac.cn + + + +Author + +Xie, Qiang +https://orcid.org/0000-0001-6376-8808 +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China +xieq8@mail.sysu.edu.cn + +text + + +Biodiversity Data Journal + + +2024 + +2024-04-05 + + +12 + + +118110 +118110 + + + + +http://dx.doi.org/10.3897/BDJ.12.e118110 + +journal article +http://dx.doi.org/10.3897/BDJ.12.e118110 +1314-2828-12-e118110 +57B0CE31B4055266A115FC1275D70C79 + + + + +Olenecamptus taiwanus Dillon & Dillon, 1948 + + + +Notes + +Lin et al. (2021) + + + + \ No newline at end of file diff --git a/data/38/3F/87/383F87C94E352B5CFDC98DB0FDF8D9D0.xml b/data/38/3F/87/383F87C94E352B5CFDC98DB0FDF8D9D0.xml new file mode 100644 index 00000000000..2c59d7ad88d --- /dev/null +++ b/data/38/3F/87/383F87C94E352B5CFDC98DB0FDF8D9D0.xml @@ -0,0 +1,142 @@ + + + +A new species of Phintella from Angola (Araneae: Salticidae) + + + +Author + +Wanda Wesołowska + +text + + +Genus + + +2010 + +21 + + +111 +114 + + + +journal article + + + + + + + +Phintella lunda + +sp. n. + + + + + +Figs 1-9 type material + + + + +Holotype +: +male +, +Angola +, +prov. Lunda Sul +, +Nova Chavez +, +10°40´S +21°20´E +, + +15.IX.1949 + +, leg. +B. Malkin +[ +California Academy of Sciences +, +San Francisco +] + + +Paratypes +: together with holotype, +4 ♀♀ +; +Angola +, +prov. Lunda Sul +, +Saurimo +, +9°40´S +21°40´E +, + +20.IX.1949 + +, +1♂ +, leg. +B. Malkin +[ +CAS +]. + + + + +diagnosis +The male of the species is easily separable from congeners by the shape of bulb, which has straight posterior edge, whereas in other species the bulb has triangular posterior lobe. The female has longer and thinner seminal ducts than other members of the genus, also shape of receptacles has characteristic utricle shape (spherical in other species). + + +etymology +The specific name is noun in apposition, referring to the type locality. + + +description +Measurements [male/female]. Cephalothorax: length 1.9/1.7-1.9, width 1.3/1.1-1.3, height 0.5/0.4-0.5. Abdomen: length 2.2/2.0-2.7, width 1.1/1.0-1.3. Eye field: length 0.9/0.8-0.9, anterior and posterior width 1.1/1.1. + +Male. General appearance in Figs1, 2. Medium sized, elongated and thin spider. Shape of body similar to the members of the genus + +Pseudicius +Simon, 1885 + +. Carapace oval, elongated, flattened, dark brown with black rings surrounding eyes. Two darker patches in centre of ocular area. Colourless hairs on carapace, long brown bristles near eyes, fawn scales fringe eyes of first row. White hairs form thin transverse stripe on eye field at base of anterior eyes, the stripe extends along sides of ocular area to eyes of last row (Fig. 2). Sides of carapace bordered by white, but thin black line along margins. Light median streak on streak on thoracic part. Clypeus very low, dark. Labium and maxillae brown, external margins of maxillae extended in triangular lobe. Sternum brown. Chelicerae large, long, with sclerotized keel on dorsum, cheliceral dentition as in Fig. 3. Abdomen elongated, ovoid, grayish brown with light median streak, two narrower streaks on sides, anterior edge also light (Fig. 2). Short hairs on abdomen, denser and longer at anterior margin. Venter yellowish gray, darker laterally, with two central lines formed by dark dots. Spinnerets long, brownish. First leg longer and thicker than remaining (Fig. 4), brown, its tibia long with three short prolateral spines and two pairs of ventral spines on metatarsus. Legs II-IV dark yellow. Leg hairs scarce, thin. Pedipalps yellow, only base of femur, cymbium and bulb brownish. Tibial apophysis single, wide, with pointed top (Figs 6, 7). Bulb triangular, embolus short (Fig. 5). + + + +1. + +Phintella lunda + +sp. n. +: 1 – habitus of male, dorsal view + + + + +2-9. + +Phintella lunda + +sp. n. +: 2 – habitus of male, 3 – cheliceral dentition, 4 – first leg, 5 – palpal organ, ventral view, 6 - palpal organ, lateral view, 7 - palpal organ, dorsal view, 8 – epigyne, 9 – internal structure of epigyne + + +Female. Similar to male, but first leg shorter than in male and lighter colored, on its patella short retrolateral spine, spination of tibia and metatarsus as in male. Coloration glaring, pattern more contrasted than in male. Epigyne with two wide pockets at epigastric furrow, two copulatory openings placed anteriorly, close to each other (Fig. 8), in strongly sclerotized “cups”. Seminal ducts thin, with accessory glands falling into in front of receptacles (Fig. 9). + + + \ No newline at end of file diff --git a/data/38/40/2C/38402CA01728E8679A4DD755892E45DC.xml b/data/38/40/2C/38402CA01728E8679A4DD755892E45DC.xml new file mode 100644 index 00000000000..636fb44c81d --- /dev/null +++ b/data/38/40/2C/38402CA01728E8679A4DD755892E45DC.xml @@ -0,0 +1,61 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Certhia caerulea +[ +spec. nov. +] + + + +C. caerulea, remigibus rectricibusque nigris. + +Certhia caerulea. +Edw. av. +21. +t. +21. + + + + + +Habitat + +Surinami. + + + + +Rostrum huic longius quam in congeneribus. + + + + \ No newline at end of file diff --git a/data/38/40/66/384066F369792E2374DEB16DBC06E413.xml b/data/38/40/66/384066F369792E2374DEB16DBC06E413.xml new file mode 100644 index 00000000000..2f73f33b1a6 --- /dev/null +++ b/data/38/40/66/384066F369792E2374DEB16DBC06E413.xml @@ -0,0 +1,56 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828-4-9042 + + + + +Syndipnus lateralis (Gravenhorst, 1829) + + + + +Tryphon lateralis +Gravenhorst, 1829 + + +punctiscuta +Thomson, 1894 + + + +Distribution +England, Scotland + + + \ No newline at end of file diff --git a/data/38/40/AF/3840AF33B67DAFF2530F6DE9F91F6B12.xml b/data/38/40/AF/3840AF33B67DAFF2530F6DE9F91F6B12.xml new file mode 100644 index 00000000000..e567db02b17 --- /dev/null +++ b/data/38/40/AF/3840AF33B67DAFF2530F6DE9F91F6B12.xml @@ -0,0 +1,149 @@ + + + +Review of the spore-feeding Idolothripinae from China (Thysanoptera, Phlaeothripidae) + + + +Author + +Dang, Li-Hong + + + +Author + +Qiao, Ge-Xia + +text + + +ZooKeys + + +2013 + +345 + + +1 +28 + + + + +http://dx.doi.org/10.3897/zookeys.345.6167 + +journal article +http://dx.doi.org/10.3897/zookeys.345.6167 +1313-2970-345-1 + + + + +Megathrips Targioni-Tozzetti + + + +Remarks. + +There are seven species listed in this genus, of which two, + +Megathrips +lativentris + +and +Megathrips antennatus +, are recorded from northern China. The original description of +Megathrips antennatus +states that it differs in having the pelta divided into three parts in contrast to the European species +Megathrips lativentris +that has the two lobes narrowly joined to the median one (Figs 25, 26). However, we studied the types of +Megathrips antennatus +, and in one paratype the left lobe of the pelta is separated from median one but the right lobe is narrowly joined to the median one. Furthermore, a female and a male from England studied in ANIC show that the lateral lobes of pelta slightly joined to the median one, or close to separate (Fig. 47). As a result, +Megathrips antennatus +Guo, Feng & Duan (2005) is here considered to be a new synonym of +Megathrips lativentris +(Heeger). +Mound and Palmer (1983) +indicated that +Megathrips +could be distinguished from +Bactrothrips +only by the slightly larger head and more deeply retracted stylets. However, in China, +Megathrips +and +Bactrothrips +species are similar in having the stylets short and V-shaped, but the lateral lobes of the pelta are broadly fused to the median lobe in +Bactrothrips +species whereas these lateral lobes are separate or narrowly joined in +Megathrips +species ( +Dang and Qiao 2012a +). + + + +Diagnosis. + +Head usually longer than width across eyes, slightly prolonged in front of eyes; eyes normal; interocellar, postocellar, postocular and mid-dorsal setae usually well-developed; stylets far apart; antennae 8-segmented, segment III shorter than head +width +across eyes, segment III with 2 sensoria, IV with 4; pronotal major setae usually well developed, anteroangulars close to midlaterals, notopleural sutures incomplete; basantra present; mesopraesternum boat-shaped; metathoracic sternopleural sutures absent; wings usually fully developed with numerous duplicated cilia; fore tarsal tooth absent in both sexes; pelta always broad, lateral lobes narrowly joined to median major lobe, or separated; abdominal tergites +II-VII +each with 2 pairs of sigmoid wing-retaining setae in macroptera; tergite VI with a pair of long lateral tubercles in male, tubercles on VIII small; tube usually shorter than head, with numerous lateral setae; anal setae shorter than tube. + + + +Figures 40-46. +Idolothripinae +genera. 40 +Gastrothrips +, head, pronotum & foreleg 41 +Bolothrips +, ventral view of head 42 +Phaulothrips +, head 43 +Megathrips +, head, pronotum & foreleg 44 +Cryptothrips +, head & pronotum 45 +Allothrips +, maxillary palps with stout terminal sensoria 46 +Gastrothrips +, antennal segments +III-VIII +. + + + + +Figures 47-54. +Idolothripinae +genera. 47 +Megathrips lativentris +, pelta 48 +Ethriothrips +, pelta 49 +Gastrothrips +, pelta 50 +Mecynothrips +, abdominal tergite IV 51 +Megathrips +, male abdominal tergites +VI-X +52 +Ethirothrips +, abdominal tergites +IV-V +53 +Compsothrips +, ventral view of thorax 54 +Meiothrips +, male abdominal tergites +IX-X +. + + + + + \ No newline at end of file diff --git a/data/38/40/E7/3840E7BCCC2D83FA7BC72A94BE62D630.xml b/data/38/40/E7/3840E7BCCC2D83FA7BC72A94BE62D630.xml new file mode 100644 index 00000000000..ae60f4dff5d --- /dev/null +++ b/data/38/40/E7/3840E7BCCC2D83FA7BC72A94BE62D630.xml @@ -0,0 +1,124 @@ + + + +Recent noteworthy findings of fungus gnats from Finland and northwestern Russia (Diptera: Ditomyiidae, Keroplatidae, Bolitophilidae and Mycetophilidae) + + + +Author + +Jakovlev, Jevgeni + + + +Author + +Salmela, Jukka + + + +Author + +Polevoi, Alexei + + + +Author + +Penttinen, Jouni + + + +Author + +Vartija, Noora-Annukka + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1068 +1068 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1068 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1068 +1314-2828--1068 + + + + + +Docosia tibialis +Lastovka +& +Sevcik +, 2006* + + + + +Materials + + +Type status: +Other material +. Occurrence: recordedBy: +R.Tuomikoski +; individualCount: +1 +; sex: +male +; Location: country: +Finland +; stateProvince: Satakunta; municipality: +Kokemaeki +; decimalLatitude: +61.254 +; decimalLongitude: +22.317 +; geodeticDatum: WGS84; Identification: identifiedBy: +J.Jakovlev +; Event: samplingProtocol: +Sweep netting +; eventDate: +1953 +; Record Level: institutionCode: +MZHF + + + + +Distribution + +European. Described recently from Czech Republic and Italy ( + +Lastovka +and +Sevcik +2006 + +), and later recorded from Sweden ( +Kjaerandsen 2012 +) and northwest Russia ( +Polevoi 2010 +). New for Finland. + + + +Ecology +Immature stages are unknown. + + + \ No newline at end of file diff --git a/data/38/41/5B/38415B13FFBB352C151EFC563478F7BA.xml b/data/38/41/5B/38415B13FFBB352C151EFC563478F7BA.xml new file mode 100644 index 00000000000..530b1e92e96 --- /dev/null +++ b/data/38/41/5B/38415B13FFBB352C151EFC563478F7BA.xml @@ -0,0 +1,122 @@ + + + +SEM morphological study of the Late Triassic clam shrimp Shipingia hebaozhaiensis (Spinicaudata, Crustacea) from Yunnan, southwestern China + + + +Author + +LI, GANG + +text + + +Palaeoentomology + + +2022 + +2022-08-15 + + +5 + + +4 + + +298 +304 + + + + +http://dx.doi.org/10.11646/palaeoentomology.5.4.2 + +journal article +10.11646/palaeoentomology.5.4.2 +2624-2834 +CABBCB06-AECC-4431-B776-AC60AF2433F2 + + + + + + +Genus + +Shipingia +Shen + +in + +Zhang +et al +., 1976 + + + + + + + + + +Type +species. + + +Shipingia hebaozhaiensis +Shen + +in + +Zhang +et al +., 1976 + +, from the +Upper Triassic Ganhaizi Formation +of +Yunnan +, +China + +. + + +Emended diagnosis. +Carapace small or medium in size, rounded, oval or elliptical in outline. Dorsal margin long and straight, small umbo located at its anterior part. Growth bands wide in the upper part of the carapace, and narrow near the ventral margin. Growth bands near the umbo ornamented with irregularly arranged small and large sized reticulations. Growth bands in the middle part of the carapace ornamented with large sized reticulations in the upper part, and small sized reticulations in the lower part of each band. Growth bands near the venter ornamented with small sized reticulations. + + +Locality and horizon. +The middle Arnstadt Formation, the upper Stubensandstein Formation in +Germany +; the middle Groveton Member of the Bull Run Formation in Culpeper Basin, the Heidlersburg Member of the middle Gettysburg Shale Formation in Gettysburg Basin, the middle and upper Passaic Formation in the Newark Basin in the +United States +; the upper Blomidon Formation in the Fundy Basin in +Canada +; the Ganhaizi Formation in Shiping County of +Yunnan Province +, +China +. + + + + +Remarks. +In the original description of + +Shipingia +Shen + +in +Zheng +et al +., 1976 only large sized reticulations were mentioned on growth bands near the umbo. According to the new SEM micrography, small and large sized reticulations are irregularly arranged on growth bands near the umbo. + + + + \ No newline at end of file diff --git a/data/38/41/5B/38415B13FFBB352C16BCF9283496FC38.xml b/data/38/41/5B/38415B13FFBB352C16BCF9283496FC38.xml new file mode 100644 index 00000000000..7b32916064f --- /dev/null +++ b/data/38/41/5B/38415B13FFBB352C16BCF9283496FC38.xml @@ -0,0 +1,151 @@ + + + +SEM morphological study of the Late Triassic clam shrimp Shipingia hebaozhaiensis (Spinicaudata, Crustacea) from Yunnan, southwestern China + + + +Author + +LI, GANG + +text + + +Palaeoentomology + + +2022 + +2022-08-15 + + +5 + + +4 + + +298 +304 + + + + +http://dx.doi.org/10.11646/palaeoentomology.5.4.2 + +journal article +10.11646/palaeoentomology.5.4.2 +2624-2834 +CABBCB06-AECC-4431-B776-AC60AF2433F2 + + + + + + +Family + +Shipingiidae +Kozur & Weems, 2005 + + + + + + + +Emended diagnosis. +Carapace small or moderate in size, with a distinct posterodorsal corner. The slightly convex umbo is narrow and small, located in the anterior part of the long and straight dorsal margin. Number and width of growth bands are variable. Microsculpture distinct, consisting in part of small and large sized reticulations and irregular radial lirae, though sometimes the reticulation may be arranged in oblique stripes or parallel to the growth lines. + + + + +Remarks. + +Shipingia +Shen + +in + +Zhang +et al +., 1976 + +was originally assigned to the family + +Loxomegaglyptidae +Novozhilov, 1958 + +, which was elevated from the subfamily + +Loxomegaglyptinae +Novozhilov, 1958 + +by + +Zhang +et al +. (1976) + +, to include taxa bearing medium- to large-sized reticulations (mesh diameter between 20 and 200 µm). The +type +genus + +Loxomegaglypta +Novozhilov, 1958 + +was considered possessing large-sized, hexagonal reticulations (mesh diameter between 50 and 100 µm) according to the text-fig. 4 of +Novozhilov (1958) +. Recently, an SEM study on the +type +specimen of + +Loxomegaglypta wetlugiana +Novozhilov, 1958 + +has clearly revealed a sieve-like fine pit ornamentation on growth bands (mesh diameter between 15 and 25 µm), which is much smaller than originally considered ( +Li, 2020c +). Thus, the author follows the opinion of +Kozur & Weems (2005) +, to remove + +Shipingia + +and + +Anyuanestheria +Zhang & Chen + +in + +Zhang +et al +., 1976 + +from +Loxomegaglyptidae +, and allocate them to + +Shipingiidae +Kozur & Weems (2005) + +. +Kozur & Weems (2005) +also assigned + +Laxitextella +Kozur, 1982 + +and +Redondestheria +Kozur, Weems & Lucas +in +Kozur & Weems, 2005 +to the family +Shipingiidae +. + + + + \ No newline at end of file diff --git a/data/38/41/5B/38415B13FFBB352C16BCFBCF3267F9EF.xml b/data/38/41/5B/38415B13FFBB352C16BCFBCF3267F9EF.xml new file mode 100644 index 00000000000..0acb99faaf5 --- /dev/null +++ b/data/38/41/5B/38415B13FFBB352C16BCFBCF3267F9EF.xml @@ -0,0 +1,90 @@ + + + +SEM morphological study of the Late Triassic clam shrimp Shipingia hebaozhaiensis (Spinicaudata, Crustacea) from Yunnan, southwestern China + + + +Author + +LI, GANG + +text + + +Palaeoentomology + + +2022 + +2022-08-15 + + +5 + + +4 + + +298 +304 + + + + +http://dx.doi.org/10.11646/palaeoentomology.5.4.2 + +journal article +10.11646/palaeoentomology.5.4.2 +2624-2834 +7333418 +CABBCB06-AECC-4431-B776-AC60AF2433F2 + + + + + +Superfamily +Eosestherioidea Zhang & Chen +in + +Zhang + +et +al + +., 1976 + + + + + + +Diagnosis. +The carapace outline is rounded, elliptical, ovate, oblong or rhombic. The umbo is small, located in the anterior part of the dorsal margin. Growth bands sparse or numerous; those near the umbo are ornamented with polygonal reticulations, which can transform to radial lirae on growth bands near the ventral margin ( +Li, 2020c +). + + + + +Remarks. +Chen and Shen (1985) +named the superfamily +Eosestherioidea +and credited the authorship to Zhang & Chen ( +in + +Zhang +et al +., 1976 + +). But there was no diagnosis published at that time. The above mentioned diagnosis of the superfamily +Eosestherioidea +is a summary of the included forms ( +Li, 2020c +). + + + + \ No newline at end of file diff --git a/data/38/41/5B/38415B13FFBE352916BCFF2933F8FEBB.xml b/data/38/41/5B/38415B13FFBE352916BCFF2933F8FEBB.xml new file mode 100644 index 00000000000..7f89be3f8b1 --- /dev/null +++ b/data/38/41/5B/38415B13FFBE352916BCFF2933F8FEBB.xml @@ -0,0 +1,198 @@ + + + +SEM morphological study of the Late Triassic clam shrimp Shipingia hebaozhaiensis (Spinicaudata, Crustacea) from Yunnan, southwestern China + + + +Author + +LI, GANG + +text + + +Palaeoentomology + + +2022 + +2022-08-15 + + +5 + + +4 + + +298 +304 + + + + +http://dx.doi.org/10.11646/palaeoentomology.5.4.2 + +journal article +10.11646/palaeoentomology.5.4.2 +2624-2834 +7333418 +CABBCB06-AECC-4431-B776-AC60AF2433F2 + + + + + + + +Shipingia hebaozhaiensis +Shen + +in + +Zhang +et al +., 1976 + + + + + + + +( +Figs 2 +, +3 +) + + +1976 + +Shipingia hebaozhaiensis + +sp. nov. +Shen +in +Zhang +et al +., p. 145, pl. 32, figs 1–5. + + +1985 + +Shipingia hebaozhaiensis +Shen + +: Chen & Shen, p. 107, pl. 7, figs 7, 8; text-fig. 66. + + +2007 + +Shipingia hebaozhaiensis +Shen + +: Kozur & Weems, p. 146, pl. 6, figs 1–7. + + + + +Emended diagnosis. +Carapace medium in size, elliptical in outline. Growth bands wide in the dorsal part, and narrow near the ventral margin. Growth bands near the umbo ornamented with irregularly arranged small and large sized reticulations. Growth bands in the middle part of the carapace, large sized reticulations located in the upper part of each growth band, and small sized reticulations located in the lower part of each growth band. Growth bands near the venter ornamented with small sized reticulations. + + + + + +Dimensions of the figured specimen +s. + +In order: specimen No., number of growth bands, length (mm), height (mm), height/length ratio: NIGP29859, 18, 7.4, 4.5, 0.61; NIGP29860, 7.3, 12, 4.5, 0.62. + + +Locality and horizon. +Shiping County of Yunnan Province, Upper Triassic Ganhaizi Formation; +Germany +, the middle Norian Arnstadt and Stubensandstein 2 formations; The +United States +, the middle Norian Bull Run and Gettysburg Shale formations. + + +Description. +Carapace moderate in size, elliptical in outline. Dorsal margin long and straight, small umbo located in its anterior part. Anterior and posterior margins rounded, ventral margin widely arched downward. Growth bands wide in the dorsal part, and become narrow near the ventral margin, +12 to 18 in +number. Growth bands in the dorsal part ornamented with small and large sized, polygonal reticulations ( +Figs 2B, C +, +3B, C, F +), mesh wall thin, mesh diameter 20 to 100 µm. Each growth band in the middle part of the carapace is ornamented with largesized reticulations in its upper part, and transform to small-sized reticulations in its lower part ( +Figs 2H +, +3E +). Growth bands near the ventral margin are ornamented with small-sized reticulations, mesh diameter 10 to 30 µm ( +Figs 2E, G +, +3G, H +). + + + + +Remarks. +Three species of + +Shipingia + +were originally described from the Upper Triassic Ganhaizi Formation: + +Shipingia hebaozhaiensis +Shen + +in + +Zhang +et al +., 1976 + +, + +S. baxinensis +Shen + +in + +Zhang +et al +., 1976 + +, + +S. xinjieensis +Shen + +in + +Zhang +et al +., 1976 + +. They differ from each other by their carapace outline. + +Shipingia hebaozhaiensis + +is elliptical, + +S. baxinensis + +is oval, and the small + +S +. +xinjieensis + +is rounded in outline. Considering that the three species are associated together in the same horizon, they may be the same species, and the outline difference may indicate sexual dimorphism or the effects of preservational distortion. Further taxonomic SEM restudy on the latter two species is needed. + + + + \ No newline at end of file diff --git a/data/38/41/87/384187FDA875FF92FC07FA21FCCD12F6.xml b/data/38/41/87/384187FDA875FF92FC07FA21FCCD12F6.xml new file mode 100644 index 00000000000..62fc92e8099 --- /dev/null +++ b/data/38/41/87/384187FDA875FF92FC07FA21FCCD12F6.xml @@ -0,0 +1,338 @@ + + + +Nova espécie de Euschistus (Mitripus) da Argentina e sul do Brasil (Hemiptera, Pentatomidae, Pentatominae) + + + +Author + +Bunde, Paulo Roberto S. +Programa de Pós-Graduação em Biologia Animal, Departamento de Zoologia, Instituto de Biociências, Universidade Federal do Rio Grandedo Sul, Av. Bento Gonçalves, 9500, Bloco IV, Prédio 43435, 91501 - 970, Porto Alegre, RS, Brasil. +paulobunde@ig.com.br + + + +Author + +Grazia, Jocélia +Programa de Pós-Graduação em Biologia Animal, Departamento de Zoologia, Instituto de Biociências, Universidade Federal do Rio Grandedo Sul, Av. Bento Gonçalves, 9500, Bloco IV, Prédio 43435, 91501 - 970, Porto Alegre, RS, Brasil. +jocelia@ufrgs.br + + + +Author + +Mendonça Junior, Milton de S. +Programa de Pós-Graduação em Biologia Animal, Departamento de Zoologia, Instituto de Biociências, Universidade Federal do Rio Grandedo Sul, Av. Bento Gonçalves, 9500, Bloco IV, Prédio 43435, 91501 - 970, Porto Alegre, RS, Brasil. +milton.mendonca@ig.com.br + +text + + +Iheringia, Sér. Zool. + + +2006 + +2006-09-30 + + +96 + + +3 + + +289 +291 + + + +journal article +10.1590/s0073-47212006000300003 +9e2df40b-14b5-4333-a904-a1a74cd8c5a3 +3585808 + + + + + + + +Euschistus +( +Mitripus +) +irroratus + +sp. nov. + + + + + + +( +Figs. 1-10 +) + + +Etimologia. Latim, +irrorare += orvalhar; alusivo ao aspecto “orvalhado” da face dorsal. + + +Distribuição. +Brasil +(Rio Grandedo Sul), +Argentina +( +Misiones +). + + + + +Material-tipo. + +Holótipo +, +BRASIL +, + +Rio Grandedo Sul + +: +Canguçu +( +Rincão da Ronda +), + +16.X.2003 + +, +P. Bunde & J. Cabeleiracol +. ( +MCNZ +) + +. + +Parátipos. Mesma procedência do holótipo, +4 +,, + +16.X. 2003 + +, +P. Bunde & J. Cabeleiracol +. ( +DZRS +) + +;, + + +07.II.2003 + +, +P. Bunde & C. Schwertner +col. ( +DZRS +) + +; + +Pelotas +,, + +25.X.1976 + +, +E. Bassan +col. ( +MECB +) + +. + +ARGENTINA +, + +Misiones + +:, + +04.II.1942 + +, +H. L. Parker +( +SAP +Lab 647 LotNo 42-7933 – +NMNH +) + +;, + +s/ data (12049 – +MACN +) + +. + + + +Descrição. Macho. Medidas: comprimento da cabeça 0,75 (0,69-0,84); largurada cabeça 1,67 (1,53-1,69); distância interocular 1,17 (1,15-1,23); comprimento do pronoto 1,52 (1,38-1,69), largura do pronoto 3,43 (3,30- 3,46); largura do pronoto com espinho 4,70 (4,61-5,15); comprimento do escutelo 2,61 (2,53-2,69); largura do escutelo 2,76 (2,56-2,92); larguraabdominal 4,40 (4,23- 4,53); comprimentototal 6,29 (6,15- 6,53). + +Antenas castanho-amareladas. Face dorsal castanho-clara e densamente pontuada. Cabeça, metade anterior do pronoto, ângulos umerais e quarto basal da margem costal do cório negros a negro-ferrugíneos. Ângulos umerais do pronoto pouco desenvolvidos e truncados na extremidade ( +Figs. 1 +, +2 +). Cicatrizes do pronoto lisas, imaculadas. Base do escutelo com duas áreasarredondadas com pontuação negra. Conexivo com pontuação negra nos ângulos anteriores e posteriores de cada segmento. Restante da pontuação da face dorsal castanho-clara. Face ventral amarelada, com densa pontuação concolor. Pernas amareladas, com pontuação castanho-escura; terço distal das tíbias e tarsos amareloferrugíneos. + + +Genitália. Pigóforo com o bordo ventral escavado em “U” amplamente aberto, comterço mediano bi-sinuado ( +Figs. 3, 5 +). Taça genital com duas carenas laminares menos desenvolvidas que em + +E +. ( +M +.) +paranticus + +, +sendo que apenas as carenas dorsais são visíveis dorsalmente no pigóforo ( +Fig. 3 +). Parâmeros em forma de foice, com a região do pé mais alargada do que em + +E +. ( +M. +) +hansi + +e + +E +. ( +M +) +paranticus + +( +Fig. 4 +). +Phallus +: conjuntiva ampla, com dois pares de processos lobados, um ventral e outro dorsal, encobrindo totalmente os processos da +phallotheca +e o +ductus seminis distalis +( +Figs. 6-8 +) + +Fêmea. Medidas: comprimentoda cabeça 0,84 (0,76- 0,92); largura da cabeça 1,80 (1,76-1,84); distância interocular 1,22 (1,15-1,30); comprimento dopronoto 1,80 (1,69-1,92), largura do pronoto 3,76 (3,69-3,84); largura do pronoto com espinho 5,30 (5,23-5,38) comprimentodo escutelo 2,88 (2,76-3,00); largurado escutelo 3,07 (3,07- 3,07); larguraabdominal 4,53 (4,46-4,61) comprimentototal 6,84 (6,76- 6,92). + +Genitália. Gonocoxitos 8 com os bordos pósterolaterais côncavos sobre os laterotergitos 9, contínuos com o bordo posterior, diferindode + +E +. ( +M. +) +hansi + +e + +E +. ( +M +.) +paranticus + +, que apresentam bordo posterior truncado ( +Fig. 9 +). +Capsula seminalis +dilatada no terço basal e digitiforme nos 2/3 apicais, mais longa que a +pars intermedialis +( +Fig. 10 +). + + + + +Planta-hospedeira. Os exemplares procedentes de Canguçu, cinco machos e uma fêmea, foram coletados nos meses de fevereiro e outubro de 2003, na borda das matas de galeria, sobre + +Schinus polygamus +(Cav.) + +( +Anacardiaceae +). + + + + +Comentários. + +Euschistus +( +M. +) +irroratus + +sp. nov. +se assemelha a +E +. + +( +M +.) +hansi +Grazia, 1987 +e + +a +E +. + +( +M +.) +paranticus +Grazia, 1987 + +, das quais se distingue principalmente pela forma dos ângulos umerais do pronoto, pouco desenvolvidos e truncados na extremidade. Em + +E +. ( +M. +) +hansi + +os ângulos umerais são desenvolvidos e projetados ântero-lateralmente, enquanto que em + +E +. ( +M. +) +paranticus + +são pouco desenvolvidos e arredondados no ápice. Nas fêmeas, + +Euschistus +( +M. +) +irroratus + +se distingue pela forma dos gonocoxitos 8 e nos machos, pelo terço mediano da escavação do bordo ventral do pigóforo bi-sinuado e pela forma dos parâmeros e dos processos da taça genital. + + + + \ No newline at end of file diff --git a/data/38/42/20/38422043B016D4D1A707A1A313DB93F6.xml b/data/38/42/20/38422043B016D4D1A707A1A313DB93F6.xml new file mode 100644 index 00000000000..66fd7b5a6f8 --- /dev/null +++ b/data/38/42/20/38422043B016D4D1A707A1A313DB93F6.xml @@ -0,0 +1,71 @@ + + + +Pheidole in the New World. A dominant, hyperdiverse ant genus. + + + +Author + +Wilson, E. O. + +text + +2003 +Harvard University Press + +Cambridge, MA, USA + + + +http://atbi.biosci.ohio-state.edu/HymOnline/reference-full.html?id=20017 + +book +20017 + + + + +Pheidole ariel +new species + +Types Mus. Comp. Zool. Harvard. + + +Etymology Gr ariel, airy sprite, alluding to the slender, pale yellow bodies of both castes. + + + +Diagnosis Similar to +desertorum +and +vistana +(see also the less similar +hyatti +), distinguished from these members of the +fallax +group and other members of the +diligens +group as follows. + + + +Major: pale to medium yellow; slender; antennal scape just reaching occipital border; occipital border deep, subangulate at midline; pilosity of body dorsum moderately abundant, suberect to erect, and very long; propodeal spine reduced to a denticle; pronotum and all of gaster smooth and shiny. +Minor: occiput broad and lacking nuchal collar; propodeal spine reduced to a denticle; carinulae limited to circular lines around +antennal fossae; mesopleuron and side of propodeum foveolate and opaque; rest of body smooth and shiny. +Measurements (mm) Holotype major: HW 1.46, HL 1.62, SL 1.34, EL 0.26, PW 0.72. +Paratype minor: HW 0.66, HL 0.82, SL 1.16, EL 0.22, PW 0.44. +color Major: concolorous pale to medium yellow. +Minor: concolorous pale yellow. + + +Range Known only from the type locality. + + +Biology Unknown. + + +Figure Upper: holotype, major. Lower: paratype, minor. MEXICO: 38 km south of Monclova, Puente La Muralla, Coahuila, 1280 m (Robert J. Hamton). Scale bars = 1 mm. + + + \ No newline at end of file diff --git a/data/38/42/8B/38428B70D25B2F4D7070F3D772F106DB.xml b/data/38/42/8B/38428B70D25B2F4D7070F3D772F106DB.xml new file mode 100644 index 00000000000..79a1babb883 --- /dev/null +++ b/data/38/42/8B/38428B70D25B2F4D7070F3D772F106DB.xml @@ -0,0 +1,102 @@ + + + +Faunistic diversity of spiders (Araneae) in Galichitsa mountain (FYR Macedonia) + + + +Author + +Deltshev, Christo + + + +Author + +Komnenov, Marjan + + + +Author + +Blagoev, Gergin + + + +Author + +Georgiev, Teodor + + + +Author + +Lazarov, Stoyan + + + +Author + +Stojkoska, Emilija + + + +Author + +Naumova, Maria + +text + + +Biodiversity Data Journal + + +2013 + +1 + + +977 +977 + + + + +http://dx.doi.org/10.3897/BDJ.1.e977 + +journal article +http://dx.doi.org/10.3897/BDJ.1.e977 +1314-2828-1-977 + + + + +macellus +Tibellus +Araneae +Arachnida +Arthropoda +Animalia + + + + +Tibellus macellus Simon, 1875 + + + +Distribution +European. + + +Notes + +Previously recorded from unspecified locality between Ohrid and Resen ( +Drensky 1929 +, +Drensky 1936 +). + + + + \ No newline at end of file diff --git a/data/38/42/9F/38429F97FBD95A2281CA26BB69B16978.xml b/data/38/42/9F/38429F97FBD95A2281CA26BB69B16978.xml new file mode 100644 index 00000000000..9880b622916 --- /dev/null +++ b/data/38/42/9F/38429F97FBD95A2281CA26BB69B16978.xml @@ -0,0 +1,100 @@ + + + +Moths (Insecta: Lepidoptera) of Delhi, India: An illustrated checklist based on museum specimens and surveys + + + +Author + +Komal, J. +National Pusa Collection, Division of Entomology, ICAR-Indian Agricultural Research Institute, New Delhi, India + + + +Author + +Shashank, P. R. +https://orcid.org/0000-0002-8177-6091 +National Pusa Collection, Division of Entomology, ICAR-Indian Agricultural Research Institute, New Delhi, India +spathour@gmail.com + + + +Author + +Sondhi, Sanjay +Titli Trust, 49 Rajpur Road Enclave, Dhoran Khas, near IT Park, P. O. Gujrada, Dehradun, Uttarakhand, India + + + +Author + +Madan, Sohail +Conservation Education Centre - ABWLS, Delhi Asola Bhatti Wildlife Sanctuary, Near Karni Singh Shooting Range, New Delhi, India + + + +Author + +Sondhi, Yash +https://orcid.org/0000-0002-7704-3944 +Department of Biology, Florida International University, Miami, Florida, United States of America + + + +Author + +Meshram, Naresh M. +ICAR- Central Citrus Research Institute, Nagpur, India + + + +Author + +Anooj, S. S. +National Pusa Collection, Division of Entomology, ICAR-Indian Agricultural Research Institute, New Delhi, India + +text + + +Biodiversity Data Journal + + +2021 + +2021-10-06 + + +9 + + +73997 +73997 + + + + +http://dx.doi.org/10.3897/BDJ.9.e73997 + +journal article +http://dx.doi.org/10.3897/BDJ.9.e73997 +1314-2828-9-e73997 +27E7CF017F40580CAC90AD41F6C3694C + + + + +Craspediopsis sp. + + + +Notes + +Present study; Fig. +7 +b + + + + \ No newline at end of file diff --git a/data/38/42/A2/3842A246F6EC52808FC362BCE9BCD47B.xml b/data/38/42/A2/3842A246F6EC52808FC362BCE9BCD47B.xml new file mode 100644 index 00000000000..0721a5ff66f --- /dev/null +++ b/data/38/42/A2/3842A246F6EC52808FC362BCE9BCD47B.xml @@ -0,0 +1,123 @@ + + + +Taxonomic revision of Telemidae (Arachnida, Araneae) from East and Southeast Asia + + + +Author + +Zhao, Huifeng +Hebei Key Laboratory of Animal Diversity, College of Life Science, Langfang Normal University, Langfang 065000, China & College of Life Sciences, Capital Normal University, Beijing 100048, China + + + +Author + +Li, Shuqiang +Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China +https://orcid.org/0000-0002-3290-5416 +lisq@ioz.ac.cn + + + +Author + +Zhang, Aibing +College of Life Sciences, Capital Normal University, Beijing 100048, China +zhangab2008@mail.cnu.edu.cn + +text + + +ZooKeys + + +2020 + +933 + + +15 +93 + + + + +http://dx.doi.org/10.3897/zookeys.933.38653 + +journal article +http://dx.doi.org/10.3897/zookeys.933.38653 +1313-2970-933-15 +AE87B5CF9728466BAB056BFFFED802D4 +C7F79558BB375F3482BCEABFB2F5F177 + + + + +Pinelema dengi (Tong & Li, 2008) +comb. nov. +Figures 9 +, 32 + + + + +Telema dengi +Tong and Li 2008a +: 69, figs 1C, 4A-H, 6 (♂♀); +Tong 2013 +: 73, figs 31N, 88A-H (♂♀). + + + +Type material. + +Holotype: ♂ (IZCAS), China, Hainan Province, Sanya Prefecture, Lizhigou Town, Luobi Cave, +18.3318N +, +109.5491E +, elevation ca. 46 m, 10.IV.2005, X. Han, Y. Song, G. Deng and Y. Tong leg. Paratypes: 1♂ and 2♀ (IZCAS), same data as holotype. Examined. + + + +Other material examined. +1♂ (molecular voucher, IZCAS), same data as holotype. + + +Diagnosis. + + +Pinelema dengi + +comb. nov. resembles + +P. spirulata + +but can be distinguished by the following: the cylindrical embolus (Fig. +9 +, and cf. +Tong and Li 2008a +: fig. 4B, C) (vs. twisted); the distal part of the receptacle is seven times wider than the receptacle neck (cf. +Tong and Li 2008a +: fig. 4D, E) (vs. five times). + + + +Description. + +See +Tong and Li (2008a) +. + + + +Distribution. + +China (Hainan, site 13 in Fig. +32 +), known only from the type locality. + + + + \ No newline at end of file diff --git a/data/38/43/0D/38430DFB6F9EC26ACDF452285FE07172.xml b/data/38/43/0D/38430DFB6F9EC26ACDF452285FE07172.xml new file mode 100644 index 00000000000..14533fd9309 --- /dev/null +++ b/data/38/43/0D/38430DFB6F9EC26ACDF452285FE07172.xml @@ -0,0 +1,62 @@ + + + +Keys to the blow flies of Taiwan, with a checklist of recorded species and the description of a new species of Paradichosia Senior-White (Diptera, Calliphoridae) + + + +Author + +Yang, Shih-Tsai + + + +Author + +Kurahashi, Hiromu + + + +Author + +Shiao, Shiuh-Feng + +text + + +ZooKeys + + +2014 + +434 + + +57 +109 + + + + +http://dx.doi.org/10.3897/zookeys.434.7540 + +journal article +http://dx.doi.org/10.3897/zookeys.434.7540 +1313-2970-434-57 +FD21DB91B5384F7A8BE48E9777F17CE9 + + + +Taxon classification Animalia Diptera Calliphoridae + + + +Stomorhina veterana Villeneuve, 1927 + + + +Materials. +1♂, Yingfeng (Gokansan), 19.viii.1980, K. Hara (NSMT); 1♀, Alishan-Yushan, 2,600-2,700 m, 31.x.1985, M. Iwasa (NSMT); 1♀, Hohuan-shan, Tsuifeng, 2,400 m, 23-24.vii.1985, S. Shinonaga (NSMT); 1♀, Hohuan-shan, Kunyan, 2,700 m, 23.vii.1985, S. Shinonaga (NSMT); 7♀, Meifeng, 2,130 m, 10-17.vii.1993, A. Smetana (CMNH); 1♂, Fenchihu, 4.iv.1965, R. Kano (NSMT); 1♀, Ten-chin, 23.04'03"N 120.45'13"E, 1,550 m, 23.viii.1996, C. W. Young (CMNH); 1♀, Tattaka, 10.iv.1965, T. Saigusa (NSMT); 1♂, Mt. Yui-shan, 2,700-3,500 m, 6-7.vii.1985, S. Shinonaga (NSMT); 1♀, Mt. Yui-shan, 2,700-3,500m, 6-7.VII.1985, S. Shinonaga (NSMT); 1♀, Hohuan-shan, Yuankang, 2,700m, 23.VII.1985, S. Shinonaga (NSMT); 12♀, Hohuan-shan, Tsuifeng, 2,400m, 23-24.VII.1985, S. Shinonaga (NSMT); 1♂, Fenchihu, 12.IV.1965, R. Kano (NSMT); 1♂ 1♀, Tatachia-anpu, 31.x.1985, K. Kanmiya (NSMT); 1♂, Tatachiaanpu-Paiyunshanchuan, 6.vii.1985, H. Shima (NSMT); 1♀, Alishan-Yushan, 2,600-2,700 m, 31.x.1985, M. Iwasa (NSMT); 1♀, Alishan-Yushan, 2,600-2,700 m, 31.x.1985, M. Iwasa (NSMT). + + + \ No newline at end of file diff --git a/data/38/43/19/384319FD04A3940A2CDEA178D81DB39E.xml b/data/38/43/19/384319FD04A3940A2CDEA178D81DB39E.xml new file mode 100644 index 00000000000..3f311e5d7ba --- /dev/null +++ b/data/38/43/19/384319FD04A3940A2CDEA178D81DB39E.xml @@ -0,0 +1,192 @@ + + + +Flora der Schweiz und angrenzender Gebiete. Band 2. Nymphaceae bis Primulaceae (2 nd edition) (p. 956): Ranunculaceae + + + +Author + +Hess, Hans Ernst + + + +Author + +Landolt, Elias + + + +Author + +Hirzel, Rosmarie + +text + +1976 +Birkhaeuser Verlag + + +https://doi.org/10.5281/zenodo.292251 + +book +292251 +10.5281/zenodo.292251 +3-7643-0527-4 + + + +<subSubSection id="D6414A631F3F19587D63DF80B1DE8434" pageId="null" pageNumber="22" type="nomenclature"> +<paragraph id="220E4DD777AD565B368701C8379CD2D4" pageId="null" pageNumber="22"> +<pageBreakToken id="C29F59885747D955425112B4EFD1C6B5" pageId="null" pageNumber="22" start="start">Artengruppe</pageBreakToken> +des +<taxonomicName id="BFEC9B031F2E2703C7C349EC5F5079D3" authority="L." class="Magnoliopsida" family="Ranunculaceae" genus="Aconitum" kingdom="Plantae" order="Ranunculales" pageId="null" pageNumber="22" phylum="Tracheophyta" rank="species" species="variegatum"> +Aconitum variegatum +<authorityName id="2D015CE69057AE366A4388CAD3A36A2E" pageId="null" pageNumber="22">L.</authorityName> +</taxonomicName> +</paragraph> +</subSubSection> +<subSubSection id="E144FAD090AB3D99F9BD0912D32922A9" pageId="null" pageNumber="22" type="vernacular_names"> +<paragraph id="7443876D49890281799290873C39BB63" pageId="null" pageNumber="22">Rispiger Eisenhut</paragraph> +</subSubSection> + + + +0,4-1,8 m hoch. Wurzel knollig verdickt. Zur +Bluetezeit +Blaetter +in der untern +Haelfte +des Stengels abgestorben; Stengel in der ganzen +Laenge +dicht +beblaettert +, kahl. +Blaetter +bis zum Grunde 3- oder 5teilig, meist nur am Rande zerstreut behaart. Abschnitte meist nicht +ueberlappend +; Zipfel zugespitzt. +Bluetenstand +locker, + +wenn verzweigt, dann die +endstaendige +Traube nicht +groesser +als die +seitenstaendigen +. +Bluetenstiel +entweder mit + ++/- + +abstehenden Haaren, die z. T. +Druesen +tragen, oder +vollstaendig + + +kahl +. + +Blueten +blau, violett oder +weiss +getleckt. zwischen dem untern Rand des Helms und den seitlichen +Perigonblaettern +meist eine +Luecke +vorhanden. + + +Die Artengruppe des + +A. variegatum +umfasst +mehrere Arten, die vor allem in mittel- und +suedosteuropaeischen +Gebirgen verbreitet sind. + +Darstellung der Artengruppe von +Goetz +(1967). Alle Arten sind diploid (2n = 16). + + + + + + + + + + + + + + + + + + + + +
+1. +Bluetenstiele +mit ++/- +senkrecht abstehenden Haaren, die z. T. +Druesen +tragen ( +Bluetenstiele +oft klebrig) + + +A. paniculatum + +(Nr. 3a) +
+1*. +Bluetenstiele +kahl. +
+2. Pflanze 1-1,8 m hoch. Stengel hin und her gebogen; Blattabschnitte am Grunde meist nicht bis auf den Mittelnerv +verschmaelert +; +Bluetenstand +lang, mit zahlreichen, weit voneinander entfernten, abstehenden +Aesten +, die nur wenige +Blueten +tragen + + +A. variegatum + +(Nr. 3b) +
+2*. Pflanze meist weniger als 0,7 m hoch; Stengel gerade; Blattabschnitte am Grunde bis auf den Mittelnerv +verschmaelert +; +Bluetenstand +meist kurz und wenig verzweigt + + +A. rostratum + +(Nr. 3c) +
+
+ + + +<normalizedToken id="651356485972FD94A83A6134E8042B72" originalValue="Schlüssel" pageId="null" pageNumber="22">Schluessel</normalizedToken> +zur Artengruppe des +<taxonomicName id="E9F6214CA8384F5E345AD2F509963FC9" class="Magnoliopsida" family="Ranunculaceae" genus="Aconitum" kingdom="Plantae" order="Ranunculales" pageId="null" pageNumber="22" phylum="Tracheophyta" rank="species" species="variegatum">Aconitum variegatum</taxonomicName> + + + +
+
+
\ No newline at end of file diff --git a/data/38/43/5C/38435C59971C896D68148F6BA4EE3110.xml b/data/38/43/5C/38435C59971C896D68148F6BA4EE3110.xml new file mode 100644 index 00000000000..256c15e6c13 --- /dev/null +++ b/data/38/43/5C/38435C59971C896D68148F6BA4EE3110.xml @@ -0,0 +1,118 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part G) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +529 +556 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Gerardia flava +Linnaeus + +, + +Species Plantarum +2 + +: 610. 1753 + + +. + + + +"Habitat in Virginia, Canada." RCN: 4416. + + + + +Lectotype +(Pennell in +Bull. Torrey Bot. Club +40: 409. 1913): +Kalm +, Herb. Linn. No. 764.6 ( +LINN +) + +. + + + + +Current name: + +Aureolaria flava +(L.) Farw. + +( +Scrophulariaceae +). + + + + +Note: +Blake (in +Rhodora +20: 67. 1918) chose +Clayton 91 +(BM) as +lectotype +, a specimen of + +Aureolaria virginica +(L.) Pennell + +, into the synonymy of which this name would therefore fall. However, usage follows Pennell (in +Rhodora +20: 133. 1918), who argued that the Kalm specimen (764.6 LINN) fitted +Linnaeus' +diagnosis better and should therefore be the type. It is identifiable as + +A. flava +. + +Reveal (in +Taxon +41: 143. 1992) therefore proposed the conservation of the name with the Kalm sheet as conserved type. However, the Committee for Spermatophyta (in +Taxon +43: 274. 1994) did not recommend acceptance, arguing that it was unnecessary as Pennell (1913), despite his unclear wording, had typified the name first. + + + + \ No newline at end of file diff --git a/data/38/44/12/38441214430F61808D9CD4BC3C785495.xml b/data/38/44/12/38441214430F61808D9CD4BC3C785495.xml new file mode 100644 index 00000000000..6c9abc0f66c --- /dev/null +++ b/data/38/44/12/38441214430F61808D9CD4BC3C785495.xml @@ -0,0 +1,92 @@ + + + +Order Artiodactyla + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +637 +722 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Przewalskium +Flerov 1930 + + + + + + + +Przewalskium +Flerov 1930 + +, + +C. +R +. Acad. Sci. +URSS +: 115 + + +. + + + + +Type Species: + +Cervus albirostris +Przewalski 1883 + + + + + +Species and subspecies: +1 species: + + +Species + +Przewalskium albirostris +(Przewalski 1883) + + + + + \ No newline at end of file diff --git a/data/38/44/4C/38444CC4B3A852A38BA030CEF945FE9C.xml b/data/38/44/4C/38444CC4B3A852A38BA030CEF945FE9C.xml new file mode 100644 index 00000000000..efa4c60369b --- /dev/null +++ b/data/38/44/4C/38444CC4B3A852A38BA030CEF945FE9C.xml @@ -0,0 +1,97 @@ + + + +A new species of the hitherto monospecific genus Pleonoporus Attems, 1938 (Diplopoda, Spirostreptida, Odontopygidae) + + + +Author + +Enghoff, Henrik +https://orcid.org/0000-0002-2764-8750 +Natural History Museum of Denmark, Universitetsparken 15, 2100 Copenhagen, Denmark + + + +Author + +Akkari, Nesrine +https://orcid.org/0000-0001-5019-4833 +Naturhistorisches Museum Wien, Burgring 7, 1010 Vienna, Austria +nesrine.akkari@nhm-wien.ac.at + +text + + +ZooKeys + + +2022 + +2022-08-15 + + +1117 + + +189 +202 + + + + +http://dx.doi.org/10.3897/zookeys.1117.87765 + +journal article +http://dx.doi.org/10.3897/zookeys.1117.87765 +1313-2970-1117-189 +2D882D312E764F9DAB6B62B183FFD554 +AFD911101457561FA4BD7AEA16AED6DE + + + + +Genus +Pleonoporus Attems, 1938 + + + +Diagnosis. + +Differs from all other genera of +Archepyginae +by having ozopores on body ring 5, a condition paralleled in the subfamily +Peridontopyginae +(see +Enghoff 2022 +: 128). In other characters, especially the structure of the gonopod telomere, + +Pleonoporus + +resembles the genus + +Spinotarsus + +Attems, 1909. + + + +Type species. + + +Pleonoporus robustus + +Attems, 1938, by monotypy + + + +Other included species. + + +Pleonoporus tanzanicus + +sp. nov. + + + + \ No newline at end of file diff --git a/data/38/44/6D/38446D96E8785C33B44B278839E24F7B.xml b/data/38/44/6D/38446D96E8785C33B44B278839E24F7B.xml new file mode 100644 index 00000000000..623da2a8d7d --- /dev/null +++ b/data/38/44/6D/38446D96E8785C33B44B278839E24F7B.xml @@ -0,0 +1,911 @@ + + + +Annotated checklist of the operculated land snails from Thailand (Mollusca, Gastropoda, Caenogastropoda): the family Pupinidae, with descriptions of several new species and subspecies, and notes on classification of Pupina Vignard, 1829 and Pupinella Gray, 1850 from mainland Southeast Asia + + + +Author + +Jirapatrasilp, Parin +https://orcid.org/0000-0002-5591-6724 +Animal Systematics Research Unit, Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand + + + +Author + +Sutcharit, Chirasak +Animal Systematics Research Unit, Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand +jirasak4@yahoo.com + + + +Author + +Panha, Somsak +Animal Systematics Research Unit, Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand & Academy of Science, The Royal Society of Thailand, Bangkok 10300, Thailand +somsak.pan@chula.ac.th + +text + + +ZooKeys + + +2022 + +2022-08-25 + + +1119 + + +1 +115 + + + + +http://dx.doi.org/10.3897/zookeys.1119.85400 + +journal article +http://dx.doi.org/10.3897/zookeys.1119.85400 +1313-2970-1119-1 +A3BE91C6B79344E1A886A803BF104D8B +F158A7C5261D52B69288A62F3C777CAF + + + + +Pupina artata Benson, 1856 + + + + +Figs 8E-H +, 10B +, 18A +, 21A-M +, 22 +, 23 +, 24A +, 25A-C + + + + +Pupina artata +Benson, 1856: 230. Type locality: Moulmein [Mawlamyine, Mawlamyine Township, Mawlamyine District, Mon State, Myanmar]. +Theobald 1858 +[1857]: 247, 248. Pfeiffer 1860: 142, pl. 37, figs 10-12. Sowerby I 1866: +Pupinidae +, pl. 3 (pl. 265), +Pupina +, figs 1, 2. Hanley and Theobald 1870: 4, pl. 7, fig. 5. +Stoliczka 1871 +: 151, 152. +Nevill 1878 +: 299, 300, Ava [Mandalay Region, Myanmar]; Moulmein; Buket Pondong [Gunung Pondok, Perak State, Malaysia]. +Reeve 1878 +: +Pupinidae +, pl. 1, sp. 3. +Crosse 1879 +: 340. de Morgan 1885: 413, Boukit Pondong, +Perak +; Java [doubtful]; Moulmein; Lahat, Ipoh, +Goping +, Kinta [Perak State, Malaysia]. + +von +Moellendorff +1894 + +: 155, the Samui Islands, Gulf of Siam [Samui Island, Surat Thani Province, Thailand]. +Godwin-Austen 1897 +: 38, 39, pl. 69, fig. 6, 6a, b. +Fischer and Dautzenberg 1904 +: 431, Ile Samui, golfe de Siam [Samui Island, Surat Thani Province, Thailand]. +van Benthem Jutting 1960 +: 12, a hill near the hot springs, near Tandjong Rambutan, N.E. of Ipoh, Perak. +Solem 1966 +: 12, Chieng Dao, Doi Sutep [Chiang Dao District and Doi Suthep Mountain, Chiang Mai Province, Thailand]. +Davison 1995 +: 236, 237, limestone island C, Temengor dam, Perak, Malaysia. +Chan 1998b +: 2, Ipoh, Perak. +Maassen 2001 +: 39, 40. +BEDO 2017 +: 87. +Sutcharit et al. 2018 +: fig. 5-13d. + + +Pupina artata var. blanfordiana +Nevill, 1878: 300. Type locality: Thyet Myo [Thayetmyo, Magway Region, Myanmar]; Akoutong [Akauk Taung, Pyay District, Bago Region, Myanmar]; Kamah Hill, Tongoop, & c., Arakan [Toungup, Thandwe District, Rakhine State, Myanmar]; Prome [Pyay, Bago Region, Myanmar]. + + +Pupina peguensis +[non Benson]- +Godwin-Austen 1897 +: 40, pl. 69, fig. 3, 3a-d, Kama on the right bank of the Irrawaddy, Pegu [Kamma Township, Thayet District, Magway Region, Myanmar]. +BEDO 2017 +: 93. + + +Pupina (Tylotoechus) artata +- +Kobelt 1902 +: 306, 307. +Gude 1921 +: 193. +Laidlaw 1928 +: 33. + + +Pupina (Pupina) artata +- +Hemmen and Hemmen 2001 +: 39. + + +Pupina blanfordi +[non Theobald]- +BEDO 2017 +: 89. + + +Pupina limitanea +[non Godwin-Austen]- +BEDO 2017 +: 90. +Sutcharit et al. 2018 +: fig. 5-13g. + + +Pupina +sp.- +Sutcharit et al. 2018 +: fig. 5-11a. + + + +Type material examined. + +Syntype +UMZC I.102960.A (1 shell; Figs +21A +, +22A +) from the R. McAndrew collection, labelled "Bens. col., Moulmein". + + + +Other material examined. + + +NHMUK 1906.4.4.28 (6 shells; +Figs +21J +, +22B +) from +Moulmein +, +Myanmar +. CUMZ 12001 (7 shells; Figs +21H +, +22C +) from +Khao Tham Phra Temple +, +Mueang Chiang Rai District +, +Chiang Rai Province +, +9 Jan. 2008 + +. + +CUMZ 12002 (1 shell) from +Luang Cave +, +Mae Sai District +, +Chiang Rai Province +, +23 Oct. 2015 + +. + +CUMZ 12003 (21 shells; +Figs +10B +, +18A +, +21I +, +22D +) from +Ban Ping Khong +, +Chiang Dao District +, +Chiang Mai Province +, +8 Oct. 2008 + +. + +CUMZ 12193 (4 shells) from +Ban Ping Khong +, +Chiang Dao District +, +Chiang Mai Province +, +21 Nov. 2012 + +. + +CUMZ 12190 (3 shells) from +Chiang Dao Cave +, +Chiang Dao District +, +Chiang Mai Province +, +25 Oct. 2015 + +. + +CUMZ 12004 ( +4 specimens +in ethanol) from +Bua Tong Cave +, +Mae Tang District +, +Chiang Mai Province +, +8 Oct. 2017 + +. + +CUMZ 12168 (4 shells) from +Doi Ang Khang +, +Fang District +, +Chiang Mai Province +, +24 Oct. 2015 + +. + +CUMZ 12005 (43 shells) from +Pha Daeng Cave +, +Mueang Mae Hong Son District +, +Mae Hong Son Province +, +18 Jan. 2015 + +. + +CUMZ 12006 (17 shells and +1 specimen +in ethanol; +Fig. +8E +) from +Pha Daeng Cave +, +Mueang Mae Hong Son District +, +Mae Hong Son Province +, +3 Dec. 2020 + +. + +CUMZ 12007 (7 shells) from +Tham Nam Pha Pha Ngam +Temple, +Mae Phrik District +, +Lampang Province +, +7 Jan. 2008 + +. + +CUMZ 12008 (3 shells and +4 specimens +in ethanol; +Fig. +8F +) from +Tham Nam Pha Pha Ngam +Temple, +Mae Phrik District +, +Lampang Province +, +8 Oct. 2020 + +. + +CUMZ 12009 (12 shells; +Figs +21G +, +22E +) from Phu Sang Waterfall, +Phu Sang District +, +Phayao Province +, +24 Oct. 2008 + +. + +CUMZ 12010 (5 shells) from +Phu Sang Waterfall +, +Phu Sang District +, +Phayao Province +, +19 Nov. 2012 + +. + +CUMZ 12011 (12 shells and +7 specimens +in ethanol; +Figs +21B +, +22F +) from +Thep Sathaporn Temple +, +Banphot Phisai District +, +Nakhon Sawan Province +, +17 July 2008 + +. + +CUMZ 12012 (17 shells) from +Khao Chuak Charoentham Temple +, +Ban Rai District +, +Uthai Thani Province +, +8 July 2009 + +. + +CUMZ 12013 (3 shells) from +Khao Chuak Charoentham Temple +, +Ban Rai District +, +Uthai Thani Province +, +27 Aug. 2016 + +. + +CUMZ 12014 (1 shell) from +Khao Chuak Charoentham Temple +, +Ban Rai District +, +Uthai Thani Province +, +5 Dec. 2020 + +. + +CUMZ 12015 (14 shells; +Figs +21F +, +23A +) from Khao Wong Phrommachan Temple, +Ban Rai District +, +Uthai Thani Province +, +8 July 2009 + +. + +CUMZ 12016 (5 shells) from +Tham Prathat Mueang Thep Temple +, +Ban Rai District +, +Uthai Thani Province +, +5 Dec. 2020 + +. + +CUMZ 12017 (13 shells) from +Krasae Cave +, +Sai Yok District +, +Kanchanaburi Province +, +10 Dec. 2006 + +. + +CUMZ 12173 (14 shells) from +Tham Charoentham Temple +, +Mueang Kanchanaburi District +, +Kanchanaburi Province +, +19 Aug. 2020 + +. + +CUMZ 12192 (1 shell) from +Ban Tapoepu-Wakruko +, +Umphang District +, +Tak Province +, +30 June 2015 + +. + +CUMZ 12018 (68 shells and +10 specimens +in ethanol; +Figs +21M +, +23B +) from +Tham Khao Thalu Temple +, +Chom Bueang District +, +Ratchaburi Province +, +9 Dec. 2006 + +. + +CUMZ 12019 (21 shells) from +Tham Khao Thalu Temple +, +Chom Bueang District +, +Ratchaburi Province +, +9 Dec. 2009 + +. + +CUMZ 12020 (4 shells and +6 specimens +in ethanol; +Fig. +25A +) from +Buri Ratchawanaram Temple +, +Pak Tho District +, +Ratchaburi Province +, +8 May 2017 + +. + +CUMZ 12021 (20 shells and +1 specimen +in ethanol) from +Buri Ratchawanaram Temple +, +Pak Tho District +, +Ratchaburi Province +, +18 Aug. 2020 + +. + +CUMZ 12022 ( +5 specimens +in ethanol; +Fig. +25B +) from +Golden Dragon Cave +, +Pak Tho District +, +Ratchaburi Province +, +18 Aug. 2019 + +. + +CUMZ 12023 (17 shells; +Figs +21C +, +23C +) from Tham Khiriwong Temple, +Bang Saphan District +, +Prachub Kirikhan Province +, +21 Apr. 2007 + +. + +CUMZ 12024 (147 shells) from +Tham Khiriwong Temple +, +Bang Saphan District +, +Prachub Kirikhan Province +, +29 July 2019 + +. + +CUMZ 12169 (10 shells) from +Tham Thep Nimit Temple +, +Pak Chong District +, +Nakhon Ratchasima Province +, +24 Aug. 2020 + +. + +CUMZ 12025 (28 shells) from +Tham Khao Cha Ang On Temple +, +Bo Thong District +, +Chonburi Province +, +13 Mar. 2006 + +. + +CUMZ 12026 (28 shells and +23 specimens +in ethanol; +Figs +21E +, +23D +) from +Tham Khao Cha Ang On Temple +, +Bo Thong District +, +Chonburi Province +, +17 Aug. 2006 + +. + +CUMZ 12028 (34 shells) from +Bo Thong District +, +Chonburi Province +, +9 May 2008 + +. + +CUMZ 12027 ( +2 specimens +in ethanol) from +Phromawat Temple +, +Si Racha District +, +Chonburi Province +, +19 Sept. 2020 + +. + +CUMZ 12174 (1 shell) from +Tham Khao Loi Temple +, +Khao Chamao District +, +Rayong Province +, +23 Oct. 2010 + +. + +CUMZ 12029 (85 shells and +10 specimens +in ethanol; +Fig. +8G, H +) from +Khao Tham Raet Temple +, +Tha Takiap District +, +Chachoengsao Province +, +21 May 2012 + +. + +CUMZ 12030 (3 shells) from +Khao Tham Raet Temple +, +Tha Takiap District +, +Chachoengsao Province +, +1 Mar. 2018 + +. + +CUMZ 12031 (43 shells; +Figs +21L +, +23E +) from Tham Khao Chakan Temple, +Khao Chakan District +, +Sa Kaeo Province +, +7 Apr. 2000 + +. + +CUMZ 12032 ( +7 specimens +in ethanol) from +Tham Khao Chakan Temple +, +Khao Chakan District +, +Sa Kaeo Province +, +25 Feb. 2018 + +. + +CUMZ 12033 (2 shells) from +Tham Khao Maka Temple +, +Mueang Sa Kaeo District +, +Sa Kaeo Province +, +2 Nov. 2008 + +. + +CUMZ 12034 (2 shells) from +Khao Pha Pheung Temple +, +Klong Had District +, +Sra Keo Province +, +21 May 2018 + +. + +CUMZ 12035 ( +1 specimen +in ethanol) from +Na Mueang Waterfall +, +Ko Samui District +, +Surat Thani Province +, +4 Mar. 2007 + +. + +CUMZ 12036 (10 shells) from +Wua Ta Lap Island +, +Ko Samui District +, +Surat Thani Province +, +5 Mar. 2007 + +. + +CUMZ 12037 (1 shell and +2 specimens +in ethanol; +Figs +21K +, +23F +, +25C +) from +Wua Ta Lap Island +, +Ko Samui District +, +Surat Thani Province +, +6 June 2009 + +. + +CUMZ 12038 (4 shells; +Figs +21D +, +24A +) from Tham Suea Temple, +Mueang Krabi District +, +Krabi Province +, +6 Oct. 2006 + +. + +CUMZ 12039 (4 shells) from +Khao Noi Phothiyan Temple +, +Mueang Satul District +, +Satul Province +, +31 Aug. 2015 + +. + +CUMZ 12040 (1 shell) from +Khao Rup Chang +, +Mueang Songkhla District +, +Songkhla Province +, +23 Jan. 2007 + +. + + + +Diagnosis. +Shell ovate; last whorl ca. three quarters of shell height. Apertural lip slightly thickened, not expanded. Both parietal and columellar teeth fin-shaped and slightly thickened; parietal tooth covering posterior canal; columellar tooth next to slit-like anterior canal. + + +Differential diagnosis. + + +Pupina artata + +is most similar to + +P. pallens + +and + +P. limitanea + +in shell shape, but different from + +P. pallens + +in that the basal position of the apertural lip is not widened, and different from + +P. limitanea + +by a longer last whorl, and parietal and columellar teeth and apertural lip less thickened. + + + +Distribution. + +Peninsular Malaysia, Myanmar ( +Laidlaw 1928 +; +Solem 1966 +), and throughout Thailand except in the northeastern region. + + + +Remarks. + +The type specimen of + +P. artata blanfordiana + +could not be located, so the validity of this subspecies is still unknown. The specimen identified as + +P. peguensis + +and figured in +Godwin-Austen (1897 +: pl. 69, fig. 3, 3a-d) from Kama on the right bank of the Irrawaddy River, Pegu is different from the holotype of + +P. peguensis + +(see +Tripathy and Sajan 2019 +), but similar to the type specimen of + +P. artata + +. Thus, this specimen is herein identified as + +P. artata + +. + + +The specimen of + +P. artata + +figured in +Maassen (2002 +: text-fig. 3) from Sumatra should constitute a different species as it is different from the syntype figured here in having a smaller, sharper parietal tooth revealing the posterior canal and an ear-lobe-shaped columellar tooth covering the anterior canal. Thus, those specimens should belong to the + +P. arula + +species group instead (see below). + + +All specimens from Thailand with a slightly thickened, fin-shaped parietal tooth covering the posterior canal are herein identified as + +P. artata + +. However, these specimens exhibit a variable shell size (smaller with shell height 5.4 mm, shell width 3.5 mm, to larger with shell height 8.4 mm; shell width 5.9 mm; Fig. +21A-M +). The shell shape is also variable from ovate which is similar to the syntype (Fig. +21A +), to more globose (Fig. +21F +) or more elongate (Fig. +21L +). In addition, these specimens exhibit a variation in length, outer curvature and thickness of the parietal tooth, and body colour. There is also a case of different shell colour morphs (brown and grey) within the same population (Fig. +8G, H +). Therefore, DNA data is needed to reveal the extent of genetic differentiation or cryptic diversity within the + +P. artata + +morphotype. + + + + \ No newline at end of file diff --git a/data/38/44/7D/38447DFDB65DA661E898C1F58D0C5B64.xml b/data/38/44/7D/38447DFDB65DA661E898C1F58D0C5B64.xml new file mode 100644 index 00000000000..44bf64a9b19 --- /dev/null +++ b/data/38/44/7D/38447DFDB65DA661E898C1F58D0C5B64.xml @@ -0,0 +1,185 @@ + + + +The Blattodeas. s. (Insecta, Dictyoptera) of the Guiana Shield + + + +Author + +Evangelista, Dominic A. + + + +Author + +Chan, Kimberly + + + +Author + +Kaplan, Kayla L. + + + +Author + +Wilson, Megan M. + + + +Author + +Ware, Jessica L. + +text + + +ZooKeys + + +2015 + +475 + + +37 +87 + + + + +http://dx.doi.org/10.3897/zookeys.475.7877 + +journal article +http://dx.doi.org/10.3897/zookeys.475.7877 +1313-2970-475-37 +C4ACAF17E887406AAF7C6D0155E7F392 + + + +Taxon classification Animalia Blattodea Blaberidae + + + +Epilampra opaca Walker, 1868 + + + +Materials. +Adult ♂ Figure 3B. + +Voucher +number: DECBA1845. + +GenBank accession number: KF155125. +Collection locale. CEIBA Biological Station, Madewini, Guyana. + +GPS: +6°29'N +, +58°13'W +. + +Date: 18 - August - 2012. +Collectors. Dominic A. Evangelista and William R. Kuhn. +Adult ♀ +Voucher number: DECBA1847. +GenBank accession number: KF155124. +Collection locale. CEIBA Biological Station, Madewini, Guyana. + +GPS: +6°29"N +, +58°13"W +. + +Date: 5 - August - 2011. +Collectors. Dominic A. Evangelista, Ian Biazzo, Manpreet K. Kohli, Melissa Sanchez-Herrera, Nicole Sroczinski and Jessica L. Ware. + + +Collection/ecological information. +The adult male (DECBA1845) was collected at a light trap. Adult female (DECBA1847) was collected by hand in the leaf litter by a small pond. Most late instar individuals of this species were also collected at the edge of this pond and some were collected in pitfall traps baited with beer. Early instar individuals of this species were collected from within bromeliads. + + + +Genetic +information. + + +The two adult specimens reported here, as well as three juvenile individuals (Voucher and accession numbers: DEDSM0141 - KF155097, DECBA1706 - KF155089, DECBA0205 - KF155088) have identical COI barcodes and are sister to each other on the tree. However, other individuals (similar to +Epilampra opaca +) included in the analysis (Voucher and accession numbers: DECBA0214 - KF155018, DECBA0216 - KF155017, DECBA0606 - KF155013, DECBA1101 - KF155016, DECBA0605 - KF155012, DECBA0608 - KF155015) are more genetically diverse and are only supported as monophyletic by 63% bootstrap support. + + + +Morphological identification. + +There is a great deal of intraspecific variation in the morphology of this species. Early instar nymphs are difficult to associate to later instar nymphs, all of which are entirely unrecognizable from the adults (Figure 3 +A-C +). Furthermore, there is variation within instars, where some later instar nymphs will appear to have a medially divided subgenital plate and others do not. This trait was not found to correlate with genetic differences ( +Evangelista et al. 2014 +). + + +The external morphology of this species provides little assistance in its identification, as most descriptions of it emphasize coloration that is both subtle and variable. However, the allometry of our specimens (Table 2) agree with those of +Bruijning (1959) +. A definitive identification was made by comparison of genital morphology using +Roth (1970b) +, particularly in the shape of the prepuce. + + + +Known geographic distribution. +Venezuela (unverified), Guyana, Suriname, French Guiana and Brazil + +History and synonymy. +Walker (1868) +first described both +Epilampra opaca +Walker, 1868 and +Epilampra substrigata +Walker, 1868. +Hebard (1926) +noted that +Epilampra opaca +Walker, 1868 has a highly variable morphology and may be synonymous with a few other +Epilampra +(e.g. +Epilampra conferta +Walker, 1868 syn. +stigmosa +Giglio-Tos, 1898, +Epilampra maculicollis +(Serville, 1838)). This variability is evident in the work published by +Roth (1970b) +, which shows a great deal of variation in the genital morphology, in particular for L2d. Although it is not clear if anyone before +Roth (1970b) +examined the genitalia of these two species, both +Shelford (1910) +and +Princis (1963) +considered them to be synonyms. + +Roth's +(1970b) + +photos show that, although each species is intraspecifically variable, both are distinct and separable by the shape of L2d and the prepuce. Roth himself acknowledged this and considered the species as being separate. Although we have not examined any +Epilampra substrigata +Walker, 1868, we agree with +Roth's +interpretation of the morphology and follow from his precedence in considering these separate (see +Roth 1970b +for the opinions of Princis and Gurney on the status of these two species). + + + +Figure 3. +Epilampra opaca +. A Early juvenile instar (DEDSM0141) B Late juvenile instar (DECBA1706) C Adult (DECBA1845). Scale bars approximate 1 mm. + + + + + \ No newline at end of file diff --git a/data/38/44/AC/3844AC0A35B41D5EC8FB69CE1CB8F0E0.xml b/data/38/44/AC/3844AC0A35B41D5EC8FB69CE1CB8F0E0.xml new file mode 100644 index 00000000000..cdd15ee73ca --- /dev/null +++ b/data/38/44/AC/3844AC0A35B41D5EC8FB69CE1CB8F0E0.xml @@ -0,0 +1,258 @@ + + + +Aquatic Insects from the Caatinga: checklists and diversity assessments of Ubajara (Ceara State) and Sete Cidades (Piaui State) National Parks, Northeastern Brazil + + + +Author + +Takiya, Daniela Maeda + + + +Author + +Santos, Allan Paulo Moreira + + + +Author + +Pinto, Angelo Parise + + + +Author + +Henriques-Oliveira, Ana Lucia + + + +Author + +Carvalho, Alcimar do Lago + + + +Author + +Sampaio, Brunno Henrique Lanzellotti + + + +Author + +Clarkson, Bruno + + + +Author + +Moreira, Felipe Ferraz Figueiredo + + + +Author + +Avelino-Capistrano, Fernanda + + + +Author + +Goncalves, Ines Correa + + + +Author + +Cordeiro, Isabelle da Rocha Silva + + + +Author + +Camara, Josenir Teixeira + + + +Author + +Barbosa, Julianna Freires + + + +Author + +de Souza, W. Rafael Maciel + + + +Author + +Rafael, Jose Albertino + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8354 +8354 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8354 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8354 +1314-2828-4-8354 + + + + +Neotrichia sp. 1 + + + +Materials + + +Type status: +Other material +. Occurrence: recordedBy: +Takiya, D.M. +; individualCount: +1 +; sex: +male +; lifeStage: +adult +; Location: country: +Brazil +; stateProvince: +Piaui +; municipality: Piracuruca; locality: + +Parque Nacional de Sete Cidades, Cachoeira do +Riachao + +; maximumElevationInMeters: 171; verbatimCoordinates: +4°6'28"S +, +41°40'13"W +; Identification: identifiedBy: +Allan Paulo Moreira dos Santos +; Event: samplingProtocol: +Pennsylvania light trap +; verbatimEventDate: +19.iv.12 +; Record Level: institutionCode: +DZRJ +; basisOfRecord: PreservedSpecimen + + +Type status: +Other material +. Occurrence: recordedBy: +Takiya, D.M. +; individualCount: +16 +; sex: +male +; lifeStage: +adult +; Location: country: +Brazil +; stateProvince: +Piaui +; municipality: Piracuruca; locality: +Parque Nacional de Sete Cidades, Riacho da Piedade +; maximumElevationInMeters: 169; verbatimCoordinates: +4°6'34"S +, +41°43'39"W +; Identification: identifiedBy: +Allan Paulo Moreira dos Santos +; Event: samplingProtocol: +Pennsylvania light trap +; verbatimEventDate: +19.iv.12 +; Record Level: institutionCode: +DZRJ +; basisOfRecord: PreservedSpecimen + + +Type status: +Other material +. Occurrence: recordedBy: +Takiya, D.M. +; individualCount: +1 +; sex: +male +; lifeStage: +adult +; Location: country: +Brazil +; stateProvince: +Piaui +; municipality: Piracuruca; locality: +Parque Nacional de Sete Cidades, Alojamento +; maximumElevationInMeters: 193; verbatimCoordinates: +4°5'57"S +, +41°42'34"W +; Identification: identifiedBy: +Allan Paulo Moreira dos Santos +; Event: samplingProtocol: +White sheet light trap +; verbatimEventDate: +20.iv.12 +; Record Level: institutionCode: +DZRJ +; basisOfRecord: PreservedSpecimen + + +Type status: +Other material +. Occurrence: recordedBy: +Takiya, D.M. +; individualCount: +1 +; sex: +female +; lifeStage: +adult +; Location: country: +Brazil +; stateProvince: +Piaui +; municipality: Piracuruca; locality: +Parque Nacional de Sete Cidades, Alojamento +; maximumElevationInMeters: 193; verbatimCoordinates: +4°5'57"S +, +41°42'34"W +; Identification: identifiedBy: +Allan Paulo Moreira dos Santos +; Event: samplingProtocol: +White sheet light trap +; verbatimEventDate: +20.iv.12 +; Record Level: institutionCode: +DZRJ +; basisOfRecord: PreservedSpecimen + + + + + \ No newline at end of file diff --git a/data/38/44/D9/3844D9C1CB61D639C74C0D65A95411BF.xml b/data/38/44/D9/3844D9C1CB61D639C74C0D65A95411BF.xml new file mode 100644 index 00000000000..45f1d5feba6 --- /dev/null +++ b/data/38/44/D9/3844D9C1CB61D639C74C0D65A95411BF.xml @@ -0,0 +1,238 @@ + + + +A Monograph of Conostegia (Melastomataceae, Miconieae) + + + +Author + +Kriebel, Ricardo +Department of Botany, University of Wisconsin-Madison, 430 Lincoln Drive Madison, Wisconsin 53706, USA +kriebelr@gmail.com + +text + + +PhytoKeys + + +2016 + +2016-07-20 + + +67 + + +1 +326 + + + + +http://dx.doi.org/10.3897/phytokeys.67.6703 + +journal article +http://dx.doi.org/10.3897/phytokeys.67.6703 +1314-2003-67-1 +D846EB3F7746FFFE4A469751FFEF3B22 +133270 + + + + +Conostegia brenesii Standl. +Fig. 71 + + + + + +Conostegia +brenesii + +Standl., Field Mus. Publ. Bot. 18: 801. 1938. Type: Costa Rica. Alajuela: La Palma de San +Ramon +, 1275-1300 m, 7 August 1927, A. Brenes 5577 (holotype: F!, isotypes: CR!, NY!). Note: at least one sheet bearing this number (also at NY) is of +Conostegia montana +(Sw) Don ex DC. +Schnell (1996) +. + + + +Description. + +Shrubs to small trees 1.5-4 m tall with tetragonal young stems that soon become terete and which are densely covered with stipitate-stellate trichomes; the nodal line inconspicuous to absent. Leaves of a pair equal to somewhat unequal in length. Petioles 0.6-4.9 cm. Leaf blades 5-13.2 +x +2.5-6.5 cm, 5 nerved or more commonly slightly plinerved, with the innermost pair of veins arising up to 1.5 cm above the base in opposite to sub opposite fashion, elliptic to elliptic-ovate, the base acute or obtuse, the apex acute and acuminate, the margin denticulate or entire, densely hirsute with rigid hairs on both surfaces. Inflorescence a terminal panicle 4.8-9.6 cm long branched above the base but sometimes appearing branched at the base because of multiple inflorescences arising at opposing meristems at the terminal node, accessory branches absent, the rachis greenish-purple to purple, densely covered with stipitate stellate trichomes, the bracts absent or very early deciduous, bracteoles 1-4 mm, deciduous. Flowers 5-6 merous, calyptrate, flower buds 5.2-7.51 +x +2.4-4 mm, rounded at the base, acute apically, the calycine and hypanthium portions weekly differentiated, slightly constricted at the torus; hypanthium 3-3.5 +x +2.75-3.25 mm, covered with stipitate-stellate trichomes. Petals 5-6.5 +x +6-6.25 mm, pink, light violet +or +white, obovate, spreading, rounded and emarginate, glabrous. Stamens 11-15, 6.25-7.25 mm, slightly zygomorphic, forming a 45 degree angle, the filament 3.75-4.25 mm, not evidently geniculate, white, anthers 2.5-3 +x +0.5-1 mm, linear-oblong and somewhat recurved, laterally compressed, the base sagittate, yellow, the pore 0.1-0.2 mm, terminal. Ovary 6 (-7)-locular, inferior, glabrous and elevated into a collar around the base of the style. Style 5.5-6.5 mm, bending below the stigma, distance between the anther and the stigma -0.1 - -0.3 mm, horizontal distance absent; stigma subcapitate, 1.4-1.6 mm wide. Almost mature berry 5-6 +x +5-6, probably purple at maturity like its close relatives. Seeds 0.4-0.6 mm, pyramidal, smooth. + + + +Figure 71. + +Conostegia brenesii + +. +A +Branch with inflorescence +B +Leaf abaxial surface +C +Inflorescence +D +Flower at anthesis +E +Longitudinal section of flower bud +F +Pickled flower at anthesis +G +Pickled flower at anthesis with half of the petals and stamens removed +H +Petal +I +Stamen +J +Style +K +Longitudinal section of the hypanthium. Photos of specimen vouchered +R. Kriebel 5631 +. + + + + +Distribution + +(Fig. +72 +). Endemic to cloud forests on the Caribbean slope of the Central and Tilaran cordilleras in Costa Rica, 1100-1750 m in elevation. + + + +Figure 72. +Distribution of + +Conostegia brenesii + +. + + + + +Conostegia brenesii + +is a very distinctive and narrow endemic of middle elevation cloud forests in Costa Rica. It can be easily distinguished by its dense indument of stipitate stellate hairs on all plant parts. Because of its dense indument of stipitate stel +late +hairs it is similar to + +Conostegia caelestis + +which is allopatric occurring in northern Central America. In addition, + +Conostegia brenesii + +tends to be a shrubby species whereas + +Conostegia caelestis + +tends to be a larger tree. The flowering time differs with + +Conostegia caelestis + +flowering in the first half of the year and + +Conostegia brenesii + +flowering in the second half of the year consistently from July to September. The molecular phylogeny does not place these species as sister taxa, which suggests convergent evolution in the dense stipitate stellate indument (Fig. +1 +). + +Conostegia brenesii + +falls sister to the + +Conostegia montana + +- + +Conostegia setosa + +complex in the molecular phylogeny. + + + +Specimens examined. + + + +COSTA RICA +. +Alajuela + +: Zapote, San Carlos, +Caribe watershed +, Smith 1102 (NY); + +La Palma de San +Ramon + +, Brenes 5633 (CR, NY); +San Carlos, P. N +. Juan Castro Blanco, entrando por San Vicente faldas del Cerro Platanar, +Rodriguez +et al. 6050 (INB, NY); + +Vara Blanca de +Sarapiqui + +, north slope of the +Central Cordillera +, Skutch 3161 (NY); +Forests of La Palma +, Tonduz 12580 (NY) + +. + + +Puntarenas + +: +R. B. Monteverde +, Haber 352 (CR) + +. + + + +San +Jose + + +: + +Cuenca del +Sarapiqui + +, Braulio Carrillo, cerca de el +tunel +, Kriebel 4907, 5631 (INB) + +. + + + + \ No newline at end of file diff --git a/data/38/44/F4/3844F45E3A270328968D646C85F48E04.xml b/data/38/44/F4/3844F45E3A270328968D646C85F48E04.xml new file mode 100644 index 00000000000..6a5cc0c7d95 --- /dev/null +++ b/data/38/44/F4/3844F45E3A270328968D646C85F48E04.xml @@ -0,0 +1,121 @@ + + + +Order Cetacea + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +723 +743 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Balaenoptera physalus +subsp. +physalus +Linnaeus 1758 + + + + + + + +Balaenoptera physalus +subsp. +physalus +Linnaeus 1758 + +, +Syst. Nat., 10th ed., Vol. 1: 75 + +. + + + + +Type Locality: + +"Habitat in Oceano Europeao", restricted to +Norway +, near +Svalbard +, Spitsbergen Sea by + +Thomas (1911 +a +) + + +. + + + + +Synonyms: + +Balaenoptera physalus +subsp. +antiquorum +(Fischer 1829) + +; + +Balaenoptera physalus +subsp. +boops +( +Linnaeus 1758 +) + +; + +Balaenoptera physalus +subsp. +gibbar +Lacépède 1804 + +; + +Balaenoptera physalus +subsp. +velifera +Cope 1869 + +. + + + + \ No newline at end of file diff --git a/data/38/45/06/3845065A9D18381B4525AC8FA917D64D.xml b/data/38/45/06/3845065A9D18381B4525AC8FA917D64D.xml new file mode 100644 index 00000000000..b89b3a26741 --- /dev/null +++ b/data/38/45/06/3845065A9D18381B4525AC8FA917D64D.xml @@ -0,0 +1,72 @@ + + + +Checklist of British and Irish Hymenoptera - Sawflies, ' Symphyta' + + + +Author + +Liston, Andrew D. + + + +Author + +Knight, Guy T. + + + +Author + +Sheppard, David A. + + + +Author + +Broad, Gavin R. + + + +Author + +Livermore, Laurence + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1168 +1168 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1168 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1168 +1314-2828-2-1168 + + + + +Monophadnoides Ashmead, 1898 + + + + +PSEUDOMONOPHADNUS +Malaise, 1935 + + + + \ No newline at end of file diff --git a/data/38/45/49/3845496E12BF5D8AA042A1377A0FDAF5.xml b/data/38/45/49/3845496E12BF5D8AA042A1377A0FDAF5.xml new file mode 100644 index 00000000000..a1a4ccd04b9 --- /dev/null +++ b/data/38/45/49/3845496E12BF5D8AA042A1377A0FDAF5.xml @@ -0,0 +1,92 @@ + + + +Diversity pattern of insects from Macao based on an updated species checklist after 25 years + + + +Author + +Xian, Chunlan +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China + + + +Author + +Leong, Chi Man +Department of Life Sciences, Faculty of Science and Technology, Beijing normal university - Hong Kong Baptist University United International College, Zhuhai, China & Macao Entomological Society, Estrada Coronel Nicolau de Mesquita, Macao SAR, China + + + +Author + +Luo, Jiuyang +https://orcid.org/0000-0002-2748-9534 +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China + + + +Author + +Jia, Fenglong +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China + + + +Author + +Han, Hongxiang +Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, China +hanhx@ioz.ac.cn + + + +Author + +Xie, Qiang +https://orcid.org/0000-0001-6376-8808 +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China +xieq8@mail.sysu.edu.cn + +text + + +Biodiversity Data Journal + + +2024 + +2024-04-05 + + +12 + + +118110 +118110 + + + + +http://dx.doi.org/10.3897/BDJ.12.e118110 + +journal article +http://dx.doi.org/10.3897/BDJ.12.e118110 +1314-2828-12-e118110 +57B0CE31B4055266A115FC1275D70C79 + + + + +Callopistria albistrigoides Poole, 1989 + + + +Notes + +DSPA (2022) + + + + \ No newline at end of file diff --git a/data/38/45/9E/38459E07FFA0FFC8F2DEEFB294F604FF.xml b/data/38/45/9E/38459E07FFA0FFC8F2DEEFB294F604FF.xml new file mode 100644 index 00000000000..cee9a4735bf --- /dev/null +++ b/data/38/45/9E/38459E07FFA0FFC8F2DEEFB294F604FF.xml @@ -0,0 +1,177 @@ + + + +A new species of extinct genus Electromyiomma Popov & Herczek (Hemiptera Miridae: Isometopinae) from Eocene Baltic amber, with the key to Electromyiomma species + + + +Author + +Kim, Junggon +Gyebaek-ro, Jung-gu, Daejeon, Korea + + + +Author + +Jung, Sunghoon +0000-0001-6086-0326 +Laboratory of Systematic Entomology, Department of Applied Biology, College of Agriculture and life Sciences, Chungnam National University, Daejeon, Korea & Department of Smart Agriculture Systems, College of Agriculture and Life Sciences, Chungnam National University, Daejeon, Korea Corresponding author: jung @ cnu. ac. kr; https: // orcid. org / 0000 - 0001 - 6086 - 0326 +jung@cnu.ac.kr + +text + + +Zootaxa + + +2021 + +2021-02-12 + + +4927 + + +2 + + +289 +293 + + + +journal article +7984 +10.11646/zootaxa.4927.2.9 +6b4c64d6-8993-4dfb-a6b5-d33a6807a517 +1175-5326 +4537144 +749DF610-9AF4-4CF6-81AD-1F3AEDEF38CA + + + + + + + +Electromyiomma herczeki +Kim & Jung + +, +sp. nov. + + + + + + +( +Figs. 1 +, +2 +) + + + + +Type material: +[ + +CNU +] +Holotype +: Holotype male in a 41x46x +38 mm +piece of Baltic amber ( +Fig. 1 +), with the curatorial museum code (CNUHHMF004) + +. + + + + +Diagnosis: +Differs from other congeners by the following combination of characters: body concolorous, approximately +3 mm +; compound eye slightly prominent; antennae linear; second antennal segment cylindrical, as long as 2 times third segment; third antennal segment longer than the fourth segment; posterior margin of pronotum weakly concave, lateral margin of pronotum constricted; hemelytra with tiny punctures. + + + + +Description: +Male +: Body elongate-oval, length 3.00 mm. +Coloration. +Entirely brownish, concolorous. +Surface and Vestiture +. Body generally rugous, distinctly punctate, covered with densely short pubescence; head densely punctate; antennae with short erect setae; pronotum (except for calli region) rugous with deep punctures and dense short pubescence; calli region with sparse punctures and pubescence; mesoscutum and scutellum punctate, covered with short pubescence, scutellum rugous; hemelytra with weak and small punctures, covered with short erect setae; cuneus with small punctures. +Structure. +Head: hypognathous, elongate in lateral view, anterior margin rounded in dorsal view, as high as pronotum height in lateral view; vertex relatively wide, 0.64 times as wide as single compound eye; compound eye prominent, reaching anterior margin of pronotum; ocelli large, close to each other; fovea antennalis positioned below compound eyes; antennae shorter than the body, linear; first segment shorter than the fourth segment; second segment longest, longer than the combination of the third and fourth segment; third segment longer than the fourth; proportion of first to fourth antennal segments 0.19: 0.73: 0.35: 0.28; frontal-clypeal part rather elongate; labium reaching hind coxae. Thorax: pronotum trapezoid, midline length shorter than anterior width and posterior width respectively, posterior margin concave, a mid-transverse line straight, lateral margin constricted medially, posterior angles rounded; pronotal collar thin; calli region distinctly swollen, inverted triangle shaped, with mesial dimple-like structure; scutellum large, midline more than pronotal midline length, scutellum width more than anterior pronotal width; mesoscutum largely developed, midline as long as 1/3 total scutellum midline length; lateral margin of hemelytra straight; commissure more than scutellum length; cuneus broad, inner margin straight; membrane with two cells; legs relatively short, hindfemur not reaching the apex of abdomen. Abdomen: elongate, exceeding apex of cuneus. +Genitalia +: not examined. + + +Measurements +(in mm): body length: 3.00; head length 0.36; head width including compound eyes: 0.67; vertex width: 0.16; interocular width: 0.02; first antennal segment: 0.19; second antennal segment: 0.73; third antennal segment: 0.35; fourth antennal segment: 0.28; pronotal midline length: 0.40; basal pronotal maximal width (straight): 0.97; anterior scutellar width: 0.68; scutellar midline length: 0.51; commissure length: 0.55; outer embolial margin length (straight): 1.40; maximal width across hemelytron: 0.60. + + + + + +Type +locality and stratum. + +Baltic amber from Baltic Sea Coast, further detailed information unknown; mid-Eocene (ca. 44.1 ± 1.1 Ma) ( +Wappler 2005 +). + + + + +Etymology: +Named after A. Herczek, a taxonomist for +Miridae +, especially a specialist of fossil taxa and the author of the genus + +Electromyiomma + +; a noun in the genitive case. + + + + +Remarks: +This new taxon is most similar to the congener, + +E. schultzi + +, but it can be distinguished by body smaller; head brownish; vertex wider comparing to compound eye width; antennae linear, first and second segments as thick as third and fourth; and hemelytra with weak and tiny punctures. This fossil is also similar to the individual as the female +paratype +of + +E. weitschati + +with remarks (see details in +Popov & Herczek (1992)) +, but can be easily distinguished by antennae linear, first and second segment as thick as third and fourth; and third antennal segment longer than the fourth segment. + +E. herczeki + + +sp. nov. + +can be easily distinguished from the other congeners, + +E. weitschati + +and + +E. polonicum + +by antennae linear; second segment cylindrical; and third antennal segment clearly longer than the fourth segment. + + + + \ No newline at end of file diff --git a/data/38/45/9E/38459E07FFA1FFCFF2DEECBE90C200DC.xml b/data/38/45/9E/38459E07FFA1FFCFF2DEECBE90C200DC.xml new file mode 100644 index 00000000000..b8acb7780cc --- /dev/null +++ b/data/38/45/9E/38459E07FFA1FFCFF2DEECBE90C200DC.xml @@ -0,0 +1,130 @@ + + + +A new species of extinct genus Electromyiomma Popov & Herczek (Hemiptera Miridae: Isometopinae) from Eocene Baltic amber, with the key to Electromyiomma species + + + +Author + +Kim, Junggon +Gyebaek-ro, Jung-gu, Daejeon, Korea + + + +Author + +Jung, Sunghoon +0000-0001-6086-0326 +Laboratory of Systematic Entomology, Department of Applied Biology, College of Agriculture and life Sciences, Chungnam National University, Daejeon, Korea & Department of Smart Agriculture Systems, College of Agriculture and Life Sciences, Chungnam National University, Daejeon, Korea Corresponding author: jung @ cnu. ac. kr; https: // orcid. org / 0000 - 0001 - 6086 - 0326 +jung@cnu.ac.kr + +text + + +Zootaxa + + +2021 + +2021-02-12 + + +4927 + + +2 + + +289 +293 + + + +journal article +7984 +10.11646/zootaxa.4927.2.9 +6b4c64d6-8993-4dfb-a6b5-d33a6807a517 +1175-5326 +4537144 +749DF610-9AF4-4CF6-81AD-1F3AEDEF38CA + + + + + + +Key to the species of extinct genus + +Electromyiomma + + + + + + + + +1. Antennae linear, second antennal segment cylindrical............................................................. 2 + + +–. Antennae not linear, second antennal segment distinctly clavate......................................................4 + + + + +2. First and second antennal segments thicker than others, third antennal segment as long as, or shorter than the fourth segment.....3 + + + +–. First and second antennal segment as thick as others, third antennal segment distinctly longer than the fourth segment............................................................................................... + +E. herczeki + + +sp. nov. + + + + + + + +3. Third antennal segment as long as the fourth segment...................................................... + +E. schultzi + + + + + + +–. Third antennal segment shorter than the fourth segment.................................. .. + +E. weitschati + +(female +paratype +) + +4. Third antennal segment as long as the fourth segment, lateral margin of pronotum constricted...... + +E. weitschati + +(male, +holotype +) + + + + + +–. Third antennal segment distinctly shorter than the fourth segment, lateral margin of pronotum almost straight...... + +E. polonicum + + + + + + \ No newline at end of file diff --git a/data/38/45/9E/38459E07FFA3FFC9F2DEEDC696E30173.xml b/data/38/45/9E/38459E07FFA3FFC9F2DEEDC696E30173.xml new file mode 100644 index 00000000000..3c03d80864a --- /dev/null +++ b/data/38/45/9E/38459E07FFA3FFC9F2DEEDC696E30173.xml @@ -0,0 +1,105 @@ + + + +A new species of extinct genus Electromyiomma Popov & Herczek (Hemiptera Miridae: Isometopinae) from Eocene Baltic amber, with the key to Electromyiomma species + + + +Author + +Kim, Junggon +Gyebaek-ro, Jung-gu, Daejeon, Korea + + + +Author + +Jung, Sunghoon +0000-0001-6086-0326 +Laboratory of Systematic Entomology, Department of Applied Biology, College of Agriculture and life Sciences, Chungnam National University, Daejeon, Korea & Department of Smart Agriculture Systems, College of Agriculture and Life Sciences, Chungnam National University, Daejeon, Korea Corresponding author: jung @ cnu. ac. kr; https: // orcid. org / 0000 - 0001 - 6086 - 0326 +jung@cnu.ac.kr + +text + + +Zootaxa + + +2021 + +2021-02-12 + + +4927 + + +2 + + +289 +293 + + + +journal article +7984 +10.11646/zootaxa.4927.2.9 +6b4c64d6-8993-4dfb-a6b5-d33a6807a517 +1175-5326 +4537144 +749DF610-9AF4-4CF6-81AD-1F3AEDEF38CA + + + + + + +Genus + +Electromyiomma +Popov & Herczek, 1992 + + + + + + + + + + +Electromyiomma +Popov & Herczek 1992: 242 + + +. +Type +species: + +Electromyiomma weitschati +Popov & Herczek, 1992 + +. + + + + + +Diagnosis: +Differs from other extinct genera in the subfamily +Isometopinae +by body elongated oval, moderate, approximately +3–4 mm +; dorsum punctate, rugous, covered with densely short pubescence; compound eye prominent; second antennal segment longer than the combination of third and fourth segments; vertex wide; labium reaching hind coxae; posterior margin of pronotum concave; calli distinctly swollen; mesoscutum broadly exposed; hemelytral membrane with two cells. + + + + +Description: +See +Popov & Herczek (1992) +for original description. + + + + \ No newline at end of file diff --git a/data/38/45/A5/3845A558F42A591E845147539F10C891.xml b/data/38/45/A5/3845A558F42A591E845147539F10C891.xml new file mode 100644 index 00000000000..0682c642f62 --- /dev/null +++ b/data/38/45/A5/3845A558F42A591E845147539F10C891.xml @@ -0,0 +1,186 @@ + + + +Revision of Streblocera Westwood (Hymenoptera, Braconidae, Euphorinae) from China, with the description of seven new species + + + +Author + +Li, Jun +https://orcid.org/0000-0002-2803-4080 +State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, Fuzhou, Fujian 35002, China & Key lab of Biopesticide and Chemical Biology, Ministry of Education, Fujian Agriculture and Forestry University, Fuzhou, Fujian 35002, China & Institute of Biological control, Fujian Agriculture and Forestry University, Fuzhou, Fujian 35002, China + + + +Author + +Achterberg, Cornelis van +https://orcid.org/0000-0002-6495-4853 +State Key Laboratory of Rice Biology, Ministry of Agriculture Key Lab of Agricultural Biology of Crop Pathogens and Insects, and Institute of Insect Sciences, Zhejiang University, Hangzhou 310058, China + + + +Author + +Zheng, Min-Lin +State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, Fuzhou, Fujian 35002, China & Key lab of Biopesticide and Chemical Biology, Ministry of Education, Fujian Agriculture and Forestry University, Fuzhou, Fujian 35002, China & Institute of Biological control, Fujian Agriculture and Forestry University, Fuzhou, Fujian 35002, China + + + +Author + +Chen, Jia-Hua +State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, Fuzhou, Fujian 35002, China & Key lab of Biopesticide and Chemical Biology, Ministry of Education, Fujian Agriculture and Forestry University, Fuzhou, Fujian 35002, China & Institute of Biological control, Fujian Agriculture and Forestry University, Fuzhou, Fujian 35002, China +jhchen34@163.com + +text + + +ZooKeys + + +2021 + +2021-06-16 + + +1044 + + +729 +782 + + + + +http://dx.doi.org/10.3897/zookeys.1044.59979 + +journal article +http://dx.doi.org/10.3897/zookeys.1044.59979 +1313-2970-1044-729 +96B47980D6AB4DC8AE026913A392DE30 +5537C4F09F9959DB8C9010D88752BFFF + + + + +Streblocera (Cosmophoridia) flaviceps Marshall, 1898 +Figure 1A-C + + + + +Cosmophorus flaviceps +Marshall, 1898: 208; Shenefelt 1969: 127; Tobias 1986: 237. + + +Cosmophoridia flaviceps +; Hedqvist, 1955: 237. + + +Streblocera (Cosmophoridia) flaviceps +; Belokobylskij, 1987: 162; +Chen and van Achterberg 1997 +: 105; +Belokobylskij 2000 +: 295. + + + +Material. + + +1♀ +, C +China +, +Hubei Province +, +Shennongjia +, +Hongping +, +1.viii.1988 +, +Jiangquan Yang +, average altitude + +2000 m + + +; + +1♀ +, NE +China +, +Heilongjiang Province +, +Heihe +city, +Wudalianchi +, +14.viii.2012 +, +Yingying Zhao +, average altitude + +300 m + + +; + +1♀ +, NE +China +, +Inner Mongolia Province +, +Wulanzuozhi +, +15.viii.2011 +, +Yingying Zhao +, average altitude + +1500 m + + +; + +1♀ +, SE +China +, +Fujian Province +, +Mt Wuyi +, +Dazhulan +, +23.vii.1986 +, +Jiang +, average altitude + +1500 m + + +. + + + +Biology. + +Unknown, but attracted to light ( +Papp and Rezbanyai-Reser 1996 +). + + + +Distribution. +Oriental: China (Fujian and Zhejiang) and Palaearctic: Austria, China (Hubei, Heilongjiang, Inner Mongolia), Czech Republic, Germany, Japan, Korea, Russia and Switzerland. + + + \ No newline at end of file diff --git a/data/38/45/B1/3845B10A078B5C59BE7CF046DEC75E5B.xml b/data/38/45/B1/3845B10A078B5C59BE7CF046DEC75E5B.xml new file mode 100644 index 00000000000..5d922454534 --- /dev/null +++ b/data/38/45/B1/3845B10A078B5C59BE7CF046DEC75E5B.xml @@ -0,0 +1,735 @@ + + + +Taxonomy and distribution of Taraxacum sect. Erythrosperma (Asteraceae) in Poland + + + +Author + +Wolanin, Mateusz +https://orcid.org/0000-0002-2461-5750 +Institute of Biology, University of Rzeszow, Zelwerowicza 4, 35 - 601, Rzeszow, Poland +wolaninm@wp.pl + + + +Author + +Klichowska, Ewelina +https://orcid.org/0000-0001-9641-5750 +Institute of Botany, Faculty of Biology, Jagiellonian University, Gronostajowa 3, 30 - 387, Krakow, Poland + + + +Author + +Jedrzejczyk, Iwona +https://orcid.org/0000-0003-2105-5310 +Laboratory of Molecular Biology and Cytometry, Department of Agricultural Biotechnology, Bydgoszcz University of Science and Technology, Kaliskiego 7, 85 - 796, Bydgoszcz, Poland + + + +Author + +Rewers, Monika +https://orcid.org/0000-0003-4105-3654 +Laboratory of Molecular Biology and Cytometry, Department of Agricultural Biotechnology, Bydgoszcz University of Science and Technology, Kaliskiego 7, 85 - 796, Bydgoszcz, Poland + + + +Author + +Nobis, Marcin +https://orcid.org/0000-0002-1594-2418 +Institute of Botany, Faculty of Biology, Jagiellonian University, Gronostajowa 3, 30 - 387, Krakow, Poland + +text + + +PhytoKeys + + +2023 + +2023-04-05 + + +224 + + +1 +88 + + + + +http://dx.doi.org/10.3897/phytokeys.224.99463 + +journal article +http://dx.doi.org/10.3897/phytokeys.224.99463 +1314-2003-224-1 +026C9306DB885DC4BE018A8ED6921203 + + + + +13. +Taraxacum tenuilobum (Dahlst.) Dahlst., Acta Fl. Sueciae 1: 47, 50, 85. 1921. + + + + +Taraxacum erythrospermum subsp. tenuilobum +Dahlst., Bot. Not., 1905: 167. 1905.Basionym. + + + + +Type +. + + + +Sweden +, Dalsland, Mo, Ojersbyn, on rock, +24 May 1901 +, + +P.A. Larsson + +( +lectotype +in S, designated by + +G. +Haglund in Doll + +1973: 86; isolectotype in S) + +. + + + +Description. + +Plants small to middle-sized, (5-)10-15 cm tall. +Leaves +grey-green, almost glabrous or with few barely visible hairs, approximately (5-)7-12(-15) cm long and (1.5-)2.5-3.5(-4) cm wide, usually 4-5 times longer than wide, blades narrowly oblanceolate, usually broadest in upper 1/3, with 3-7 pairs of lateral lobes; lateral lobes opposite to remote; lateral lobes of the inner leaves strongly dissected, somewhat recurved and twisted, quite often slightly widening at the apex, often with parallel small and acute lobes at the distal margin base; lateral lobes of the outer leaves narrowly triangular, slightly recurved or patent, quite often incised or toothed at the distal margin base; interlobes long, often lobulate; terminal lobe of the inner leaves elongate with a protracted apex; terminal lobe of the outer leaves tripartite-subsagitate, quite often with the apical lobule slightly widening at the apex; petioles unwinged, purple. +Scapes +as long as or shorter than leaves, hairy, especially just under the capitulum. +Capitulum +convex, 2.5-3.5 cm in diameter, yellow, outer strips grey-violet; inner bracts greyish-green, often with small lumps; outer bracts usually 10-15, narrowly lanceolate, usually 6-8 mm long, 1.5-2 mm broad, bright greyish-green, suffused with violet, faintly bordered (up to 0.05 broad), arcuate, without corniculation or sometimes with small cornicules; stigmas dark greyish-green, pollen present. +Achenes +red-brown, in the upper part with slender spinules, 3.5-4.0 mm long (incl. the 0.8-1.1 mm long, cylindrical cone), rostrum 6-7 mm long, pappus white. + + + +Flowering period. +April-May. + + +Habitat. + +In the northern part of Poland, this species grows most often in dry and sandy habitats, such as sandy grasslands, roadsides of forest roads, edges of pine fo-rests, paths, cliffs, dunes, and lawns. In southern Poland, we noticed this species most often in rock grasslands (in eroding and trampled areas). Plant communities with the participation of + +T. tenuilobum + +were predominated by species typical to the +Festuco-Brometea +(especially in S Poland) and +Sedo-Scleranthetea +classes. In +Świetokrzyskie +Mts (Miedzianka place) we noted this species in rocky grassland growing together with + +Allium montanum + +, + +Arenaria serpyllifolia + +, + +Artemisia campestris + +, +Camelina microcarpa subsp. sylvestris +, + +Campanula sibirica + +, + +Centaurea stoebe + +, + +Cerastium semidecandrum + +, + +Dianthus carthusianorum + +, + +Euphorbia cyparissias + +, + +Galium mollugo + +, + +Holosteum umbellatum + +, + +Medicago falcata + +, + +Plantago media + +, + +Poa compressa + +, + +P. pratensis + +, + +Potentilla argentea + +, + +Ranunculus bulbosus + +, + +Salvia pratensis + +, + +Sanguisorba minor + +, + +Sedum acre + +, + +Silene nutans + +, + +Stachys recta + +, + +Thymus pulegioides + +, + +Verbascum nigrum + +, + +Vincetoxicum hirundinaria + +, + +Viola arvensis + +. On the coast of the Baltic Sea ( +Leba +place) we observed these species on the sandy edge of the pine forest, accompanied by + +Carex arenaria + +, + +Cerastium semidecandrum + +, + +Erophila verna + +, + +Potentilla argentea + +, + +Vicia lathyroides + +. + + + +Somatic chromosome number. + +24 ( + +Wolanin and +Musial +2017 + +), 25 ( + +Malecka +1969 + +). + + + +General distribution. + +Mainly NE part of Europe. Species reported from Switzerland, Germany, the Netherlands, Denmark, Poland, Sweden, Norway, Crimea, Moldova, Ukraine, Latvia, Estonia and European Russia ( +Van Soest 1969 +; +Tutin et al. 1976 +; +Tacik 1980 +; +Fedorov 1989 +; + +Lundevall and +Ollgaard +1999 + +; +Mosyakin and Fedoronchuk 1999 +; +Uhlemann 2003 +; + +Wendt and +Ollgaard +2015 + +). + + + +Distribution in Poland. + +Localities grouped in 4 separate areas in northern and southern Poland; quite frequent only in Podlachia and on the coast of the Baltic Sea (Fig. +36A +). + + + +Figure 36. +Distribution maps of +Taraxacum sect. Erythrosperma +in Poland +A + +T. tenuilobum + +B + +T. tortilobum + +; black square - localities recorded during field studies, black circle - other localities known from herbarium data. + + + + +Specimens examined. + +BA59 +- + +Ustka, path, +54°35'25"N +, +16°53'07"E +, +1 May 2017 +, + +M. Wolanin + +(003309 UR); +BA76 +- +Darlowko +, sands, +54°26'45"N +, +16°23'41"E +, +1 May 2017 +, + +M. Wolanin + +(003323 UR); +BA84 +- +Lazy +, path in pine forest, +54°18'16"N +, +16°11'16"E +, +1 May 2017 +, + +M. Wolanin + +(003346 UR); +CA38 +- + +1,5 km +E of Rozewie + +, cliff, +30 May 1961 +, +Monk +/ +Mark +(152/2 UGDA); +CA43 +- +Leba +, path in pine forest, +54°46'05"N +, +17°34'06"E +, +1 May 2017 +, + +M. Wolanin + +(003336 UR); +DA60 +- south of + +Babie +Doly + +, cliff, +12 May 1970 +, + +W. Chojnacki + +(153/01 UGDA); +DA70 +- Sopot, lawn near promenade, +54°27'26"N +, +18°33'43"E +, +8 May 2016 +, + +M. Wolanin + +(003296 UR); +DA80 +- +Wisloujscie +( +Gdansk +), lawn, +54°23'37"N +, +18°40'36"E +, +7 May 2016 +, + +M. Wolanin + +(003552 UR); +DA82 +- +Świbno +, sandy roadside in forest, +54°20'18"N +, +18°56'12"E +, +10 May 2016 +, + +M. Wolanin + +(003283 UR), +DB60 +- near Jaszczerek, sandy roadside, +53°37'02"N +, +18°35'16"E +, +1 May 2019 +, + +M. Wolanin + +(003575 UR), +DF06 +- Kroczyce, grassland and paths on calceolus rock (SW slope), +50°34'18"N +, +19°31'47"E +, +1 May 2013 +, + +M. Wolanin + +(003359 UR); Podlesice, rock close to cave, grassland on rock, +50°34'30"N +, +19°31'32"E +, +1 May 2021 +, + +M. Wolanin + +(003593 UR); +Mirow +, grassland on rock overgrown by shrubs, +50°36'53"N +, +19°28'51"E +, +1 May 2021 +, + +M. Wolanin + +(003595 UR); +EE72 +- Miedzianka hill, grassland on rock, +50°50'49"N +, +20°21'32"E +, +11 April 2016 +, + +M. Wolanin + +(003514 UR); +EE83 +- +Sosnowka +hill, grassland on rock, +50°48'24"N +, +20°26'15"E +, +11 April 2016 +, + +M. Wolanin + +(003500 UR); +FB59 +- +between Wrotki and Mogielnica +, dry pasture, +53°39'45"N +, +22°58'11"E +, +24 April 2016 +, + +M. Wolanin + +(003270 UR); +FB76 +- +Sosnia +, dunes on pasture, +8 May 2003 +, + + +Z. +Glowacki + + +(0388261 KRA); +FC11 +- Czartoria, hillock close to river, +8 May 2016 +, + +T. +Gruzewska + +(MPD); +FC13 +- +Piatnica +( + +Fort +Lomza + +), pastured sandy grassland, +53°11'48"N +, +22°07'00"E +, +24 April 2016 +, + +M. Wolanin + +(003539 UR); +FC27 +- Truskolasy-Lachy, stoned field road close to old excavation, +53°02'23"N +, +22°42'11"E +, +2 May 2018 +, + +M. Wolanin + +(003481); +FC34 +- +Zbrzeznica +, psammophilous grassland, +53°01'24"N +, +22°10'11"E +, +26 April 2016 +, + +M. Wolanin + +(003546 UR); +FC73 +- +Borowe nad Bugiem +, +Bug river +sandy terrace, +52°40'22"N +, +22°00'41"E +, +26 April 2016 +, + +M. Wolanin + +(003545 UR); +FD09 +- +Buzka +, sandy roadside, +52°21'26"N +, +22°53'55"E +, +25 April 2016 +, + +M. Wolanin + +(003484 UR); +GD10 +- Serpelice, lawn, +52°16'49"N +, +23°03'01"E +, +25 April 2016 +, + +M. Wolanin + +(003257 UR); +GF00 +- Tereszpol near +Bilgoraj +, lawn, +50°33'13"N +, +22°55'54"E +, +25 April 2016 +, + +M. Wolanin + +(003468 UR); +GF24 +- +Belzec +, grassland on closed railway track, +50°22'45"N +, +23°26'51"E +, +18 April 2019 +, + +M. Wolanin + +(003587 UR) + +. + + + +Notes. + +Plant with distinct, strongly incised and narrow side lobes, and tongue-shaped terminal lobe apex. Outer phyllaries are narrowly lanceolate, arcuate, faintly bordered. Juvenile plants can be confused with + +T. scanicum + +, which has significantly less dissected side lobes, and the outer bracts of which are wider (with distinct hyaline margin, 0.1-0.2 mm broad), recurved or patent (Figs +37 +, +38 +). + + + +Figure 37. +Variation in leaf shape in + +T. tenuilobum + +; locality - Kroczyce ( +M. Wolanin +2016 UR). Scale bar: 5 cm. + + + + +Figure 38. + +Taraxacum tenuilobum + +; locality - +Leba +, 2017, photo by M. Wolanin. + + + + + \ No newline at end of file diff --git a/data/38/46/87/384687CEFF8AFF9AFF6F58F106D7DF4D.xml b/data/38/46/87/384687CEFF8AFF9AFF6F58F106D7DF4D.xml new file mode 100644 index 00000000000..f4864f9106f --- /dev/null +++ b/data/38/46/87/384687CEFF8AFF9AFF6F58F106D7DF4D.xml @@ -0,0 +1,166 @@ + + + +A new species of subgenus Eulandrevus Gorochov, 1988 (Orthoptera: Gryllidae: Landrevinae) from China + + + +Author + +He, Zhuqing + + + +Author + +Ma, Libin + +text + + +Zootaxa + + +2015 + +4013 + + +4 + + +594 +599 + + + +journal article +10.11646/zootaxa.4013.4.9 +fdef6346-a780-4b6b-b051-64ac1d2b9b31 +1175-5326 +236809 +B9F30853-A4B2-4BCB-9FBA-AD49D2B82867 + + + + + + + +Duolandrevus +( +Eulandrevus +) +unguiculatus +Ma, Gorochov & Zhang + + + + + + + + + +Duolandrevus (Eulandrevus) unguiculatus + +Ma, Gorochov & Zhang, 2015 +:446 + + + + + + + + +Type +specimen information. + +Type +locality ( +holotype +): Wangtianshu Park, Bubang, MenglaTai, Yunnan Province, +China +. Deposited at Museum of Hebei University, Baoding, Hebei Province, +China +( +MHBU +). + + + +Materials examined. +China +: + +Holotype +: male, +China +, Yunnan Prov., Mengla, Wangtianshu (Bubang), coll. Ren Guodong, Hou Wenjun and Li Yalin, 6~ +7 August 2007 +( +MHBU +). + + + + +Distribution +( +Fig. 1 +). +China +(Yunnan). + + + + +Measurements. +BL 17.5, HW 4, PL 2.5, PW 4, FWL 6, HFL 10. + + + + +Diagnosis. +Body size small for most + +Landrevinae + +species, brown. Male tegmina with a small but distinct mirror in the stridulatory apparatus. Dorsal field of forewings somewhat square and armed with arc-like margin laterally. Both inner and outer fore tibiae tympanum present. Metanotal gland shiny and smooth for a quarter of apical portion and armed with long hairs for most of base portion. Ramiform branches of epiphallic median lobes armed with claw-like apex. + + + + +Remarks +. This species was reported recently, located in Yunnan Province, +China +. Its male genitalia are very similar to those of + +D. +( +E +.) +sonorus + +in the epiphallic median lobes, having long apical lobules. But, in + +D. +( +E +.) +unguiculatus + +, the latter lobules are much longer than in + +D. +( +E +.) +sonorus + +and in all the other species of this subgenus. + + + + \ No newline at end of file diff --git a/data/38/46/87/384687CEFF8CFF9DFF6F5C8B010FDEF6.xml b/data/38/46/87/384687CEFF8CFF9DFF6F5C8B010FDEF6.xml new file mode 100644 index 00000000000..6d551b43748 --- /dev/null +++ b/data/38/46/87/384687CEFF8CFF9DFF6F5C8B010FDEF6.xml @@ -0,0 +1,195 @@ + + + +A new species of subgenus Eulandrevus Gorochov, 1988 (Orthoptera: Gryllidae: Landrevinae) from China + + + +Author + +He, Zhuqing + + + +Author + +Ma, Libin + +text + + +Zootaxa + + +2015 + +4013 + + +4 + + +594 +599 + + + +journal article +10.11646/zootaxa.4013.4.9 +fdef6346-a780-4b6b-b051-64ac1d2b9b31 +1175-5326 +236809 +B9F30853-A4B2-4BCB-9FBA-AD49D2B82867 + + + + + + + +Duolandrevus +( +Eulandrevus +) +hainanensis + +sp. n. + + + + +( +Figs. 1 +, +2 +A, 3A, 3C, 3E) + + + + + +Type +material. +Holotype +. + +male. +China +: Hainan, Jianfengling, +Jul. 22, 2009 +, coll. He Zhuqing ( +SNNU +). + + + + +Measurements. +BL 21.04, HW 5.43, PL 2.77, PW 4.91, FWL 6.78, MTL 4.58, HFL 12.59, HTL 8.75, CL>6.35 (destroyed). + + + + +Etymology. +The specific epithet “ + +hainanensis + +” refers to the location of specimen. + + + + +Diagnosis. +Large body size. Elytra shorter than uncovered abdomen portions. Six oblique veins ( +Fig. 2 +A). Apical portions armed with reticulated veins. Both inner and outer tympanum present, oval shaped. Epiphallic lateral lobes somewhat squared apically, equipped with a denticle pointed backward (Fig. 3C). + + + + +FIGURE 2. +Body, dorsal view. +A. + +D. +( +E. +) +hainanensis + +; +B. + +D. +( +E. +) +hongkongae + +. + + + + +Description. +Body size large for this genus. Head large and transverse, conspicuously wider than pronotum. Occiput broad and somewhat flattened, slightly inclined to rostrum. Rostrum broad and flattened, almost equal to the width of antennal scape. Portions under antennal socket concave and flattened, and portions under eyes concave but wrinkled. Straight rostrum suture. Labrium rhombus-like, with angle lateral margins and concave apical margin. End section of maxillary palpi longer than the third, depressed and widened, with rounded apex. End section of labrial palpi longer than remainder basal sections, depressed and widened, with truncated tip. Median ocellus small and transverse oval-like; lateral ocelli large and rounded. + + +Pronotum short, disk almost smooth, bearing few hairs; anterior margin concave and arc-like, posterior margin straight. Pronotal disk somewhat rounded and curved to lateral lobes without lateral edges. Lateral lobes vertically short, equipped with a ridge along margin and concave at hind corner beyond the ridge. +Hind +wings absent. Tegmina shorter than abdomen and with 6 oblique veins; apical portions bearing reticulated veins. + + +Both inner and outer tympanum present on fore tibia, oval-like and inner slightly larger than the outer. Fore tibiae laterally depressed. +Hind +tibiae equipped with spines proximally and with spurs halfway on the proximal portion, numbered 4:5 (inner: outer); inner apical spurs longer than the outer; ventral inner apical spur shortest, median outer apical spur longest. Abdomen armed with few hairs, almost smooth. Supra-anal plate simple, trapezoid-like with straight apex. Cercus robust, pubescent. Subgenital plate simple, fusiform, with acute apex. Genitalia: Epiphallus slightly widened and constricted apically, equipped with pair of small median lobes; lateral lobes longitudinally wide and armed with somewhat squared apex, with a denticle pointed backward. Top lobe of ectoparamere large and apically truncated in lateral view, with a rather small notch beyond the small bottom lobe. + + +Coloration ( +Fig. 2 +A). Body brown-colored. Antenna, legs, cercus and bottom of abdomen light-colored. + + +FIGURE 3. +Genitalia. A, C, E. + +D. +( +E. +) +hainanensis + +; B, D, F. + +D. +( +E. +) +hongkongae + +. A~B, dorsal view; C~D, lateral view; E~F, ventral view. + + + + +Remarks. +So far, all + +Eulandrevus + +species could be basically divided into two +types +from the shape of their epiphallic tips—simple rod-like and bifurcated. The new species is distinct from its relatives. Its epiphallic tip is simple but short, thick and somewhat square-like when laterally viewed, and also armed with a tooth pointed toward the head. Additionally, the new one is slightly larger than the previous, with longer elytra that reach the 5th abdominal tergite (that of + +D +. ( +E +.) +hongkongae + +is just extended to the apex of the 4th tergite). + + + + \ No newline at end of file diff --git a/data/38/46/87/384687CEFF8DFF9AFF6F5B590644DC9E.xml b/data/38/46/87/384687CEFF8DFF9AFF6F5B590644DC9E.xml new file mode 100644 index 00000000000..53f61633274 --- /dev/null +++ b/data/38/46/87/384687CEFF8DFF9AFF6F5B590644DC9E.xml @@ -0,0 +1,186 @@ + + + +A new species of subgenus Eulandrevus Gorochov, 1988 (Orthoptera: Gryllidae: Landrevinae) from China + + + +Author + +He, Zhuqing + + + +Author + +Ma, Libin + +text + + +Zootaxa + + +2015 + +4013 + + +4 + + +594 +599 + + + +journal article +10.11646/zootaxa.4013.4.9 +fdef6346-a780-4b6b-b051-64ac1d2b9b31 +1175-5326 +236809 +B9F30853-A4B2-4BCB-9FBA-AD49D2B82867 + + + + + + + +Duolandrevus +( +Eulandrevus +) +hongkongae +Otte, 1988 + + + + + +( +Figs. 1 +, +2 +A, 3B, 3D, 3F) + + + + + +Type +specimen information. + +Type +locality ( +holotype +): Tai Po Kai Forestry Station, +Hong Kong +, +China +. Deposited at Bishop Museum, Honolulu, Hawaii, +U.S. +(not examined). + + + +Materials examined. +China +: + +3 males +and +1 female +, Guangdong, Fengkai, Heishiding, +Oct. 3, 2014 +, coll. Zhang Tao ( +SNNU +); +1 male +, Guangdong, Zhaoqing, Dinghushan, +Oct. 5, 2014 +, coll. Zhang Tao ( +SNNU +); +2 males +, Guangdong, Zhaoqing, Jiulonghu, +Oct. 31, 2014 +, coll. Zhang Tao ( +SNNU +). + + + + +Distribution +( +Fig. 1 +). +China +(Guangdong). + + + + +Measurements. +BL 20.08±0.09, HW 5.12±0.47, PL 3.02±0.21, PW 4.94±0.30, FWL 6.36±0.38, MTL4.55, HFL 12.63±0.40, HTL 7.91±0.62, CL 12.63±1.80 + + + + +Diagnosis. +Large body size. Tegmina shorter than uncovered portions of abdomen with 5 oblique veins ( +Fig. 2 +B); apical area armed with reticulated veins. Fore tibia with both inner and outer tympanum present, roundly shaped. Epiphallic lateral lobes possessing bifurcated tips (Fig. 3D). + + + + +Description. +Body size large for genus. Head large and transversely broad. Occiput somewhat convex, longitudinally short. Vertex inclined to rostrum. Rostrum wide and flattened, as wide as antennal scape. Labrum rhombus-like with rounded margin. End section of maxillary palpi broad and depressed, with expanded apex. End section of labrial palpi depressed and angular-like, and longer than the remainder sections. + +Pronotum more pubescent and narrower than head. Pronotal anterior margin concave and arc-like; posterior margin almost straight. Pronotal disc without obvious lateral edge and roundly inclined to lateral lobes. Lateral lobe bearing a ridge along the margin and dividing hind corner. + +Hind +wings absent. Tegmina shorter than uncovered portions of abdomen with 5 oblique veins; apical area armed with reticulated veins. + + +Tympanum of fore tibia rounded, the inner larger than the outer. +Hind +tibia armed with spines halfway on the basal portion and with subapical spurs at the apical portion, numbered as 4:4 (inner: outer). + +Abdomen pubescent, armed with thin, dense and binding hairs. Supra-anal plate simple and trapezoid-like. Subgenital plate fusiform with acute tip. Cercus narrowing apically, armed with long hairs, binding hairs and shield-like hairs. Genitalia: Epiphallus somewhat narrowed and constricted gradually toward apex. Epiphallic median lobes paired, small and apically acute; epiphallic lateral lobes bifurcate apically. Epiphallic proximal margin bisinuate. Ectoparamere bifurcate into top and bottom lobes and present a notch between lobes. Top lobe rounded but subacute, with a shallow and broad notch. + +Coloration ( +Fig. 2 +B). Body brownish, light-colored in antennal scape, legs and the dorsum of elytra. + + + + +Remarks +. + +D +. ( +E +.) +hongkongae + +was reported from +China +and + +D +. ( +E +.) +dendrophilus + +reported from +Vietnam +. They are very similar in shape at the apical ends of the epiphallic lateral lobes. Both of their tips are bifurcated and pointed upward; only the outside margins at the bottom of the tips are different from each other. + + + + \ No newline at end of file diff --git a/data/38/46/87/384687CEFF8FFF9FFF6F5A6F0779DF7E.xml b/data/38/46/87/384687CEFF8FFF9FFF6F5A6F0779DF7E.xml new file mode 100644 index 00000000000..f54e028e96d --- /dev/null +++ b/data/38/46/87/384687CEFF8FFF9FFF6F5A6F0779DF7E.xml @@ -0,0 +1,83 @@ + + + +A new species of subgenus Eulandrevus Gorochov, 1988 (Orthoptera: Gryllidae: Landrevinae) from China + + + +Author + +He, Zhuqing + + + +Author + +Ma, Libin + +text + + +Zootaxa + + +2015 + +4013 + + +4 + + +594 +599 + + + +journal article +10.11646/zootaxa.4013.4.9 +fdef6346-a780-4b6b-b051-64ac1d2b9b31 +1175-5326 +236809 +B9F30853-A4B2-4BCB-9FBA-AD49D2B82867 + + + + + + +Subgenus + +Eulandrevus +Gorochov, 1988 + + + + + + + + +Type +species. + + +Eulandrevus sonorus +Gorochov, 1988 + + + + + +Diagnosis. +Head depressed dorsoventrally. Elytra bearing developed stridulatory apparatus and protracted lateral area. Fore tibiae armed with both inner and outer tympana, sometimes one of them absent. +Hind +tibiae possessing dorsal spines in both +types +of long, articulated and short, unarticulated. Epiphallus equipped with distinct transverse fold or a pair of lateral folds in middle. Posterolateral lobes not plate-like, widened and lacking denticles ( +Ma et al., 2015 +). + + + + \ No newline at end of file diff --git a/data/38/46/DC/3846DCF2BCB7A8CB5F35DE025E8B92D5.xml b/data/38/46/DC/3846DCF2BCB7A8CB5F35DE025E8B92D5.xml new file mode 100644 index 00000000000..91615233830 --- /dev/null +++ b/data/38/46/DC/3846DCF2BCB7A8CB5F35DE025E8B92D5.xml @@ -0,0 +1,141 @@ + + + +Agra, arboreal beetles of Neotropical forests: pusilla group and piranha group systematics and notes on their ways of life (Coleoptera, Carabidae, Lebiini, Agrina) + + + +Author + +Erwin, Terry L. +Washington DC +erwint@si.edu + +text + + +ZooKeys + + +2010 + +66 + + +1 +28 + + + + +http://dx.doi.org/10.3897/zookeys.66.684 + +journal article +http://dx.doi.org/10.3897/zookeys.66.684 +1313-2970-66-1 +176306EB63424E75AD76C4A82040A002 +AD1FFFAF9122FFEAFF8EEF3BE966F439 +576888 + + + + +Agra pseudopusilla Erwin +sp. n. +Figs 5 +10 + + + +Holotype: + +Brazil: +(Comte G. de Mniszech)(MNHNP: ADP 060088, female). + + + +Derivation of specific epithet. + +The epithet " +pseudopusilla +" refers to the similarity between adults of this species and those of +Agra pusilla +, treated below. + + + +Proposed English vernacular name. + +Mniszech's +Elegant Canopy Beetle. + + + +Diagnosis. +With the attributes of the genus and species-group as described above and frons laterally multicarinate; occiput coarsely bi-punctate, with several smaller punctures; elytral interneurs with mostly uni-serial rows of cribriform punctures, doubled apico-laterally. + + +Description. + +( +Fig. 5 +). +Size +: Small, ABL = 6.57 - 8.63 mm, SBL = 5.67 - 7.15 mm, TW = 1.34 - 2.08 mm. +Color: +Head and pronotum black, elytra smoky black, legs bicolored, antennae and mouthparts piceous, scape with testaceous venter, piceous dorsum. +Luster: +Shiny forebody, matte elytra. +Head: +Labrum moderately elongate and truncate apically, anterior corners rounded. Frons medially raised and smooth, laterally depressed, multicarinate. Gena slightly tapered with broadly rounded corners to constricted neck in both male. Occiput coarsely bi-punctate, with several smaller punctures. +Prothorax: +Slightly broader medially, flared basally; surface with dense and coarse punctures, some setiferous; lateral elongate callous with single row of setigerous punctures along middle. +Pterothorax: +Elytron markedly convex, intervals slightly costate, interneurs of rows of somewhat laterally ovate punctures, doubled in some places, apex oblique, slightly lobed at middle, apical dentation asymmetric, lateral tooth short, acute, sutural apex not produced. Metasternum sparsely setiferous in males. +Legs: +Normal. +Abdomen +: Abdominal sterna III to VII of male moderately and bilaterally setiferous; sternum VII of males barely emarginate, corners rounded. +Male genitalia: +Phallus ( +Fig. 5 +) elongate and narrow with ostium not elongate, extended to about 1/2 the length of phallus, apex a small rounded +lobe +. Parameres small, left twice the size of the right, both moderately rounded. +Female ovipositor: +Female unknown + + + +Dispersal potential. +These beetles are macropterous and are probably capable of flight; they are swift and agile runners. + + +Way of life. + +Adults of other +Agra +species are found in the canopy of rainforest trees; known larvae of this genus ( +Arndt et al. 2001 +) are found under the bark of these trees, however they must also roam on the surface, as they have been collected by insecticidal fogging techniques in the very early morning before first light. Members of +Agra pseudopusilla +are labeled Brazil without further information. + + + +Other specimens examined. + +Brazil: +(Ehrenreiche)(BNCRio: ADP 070045, male paratype). + + + +Geographic distribution. + +( +Fig. 10 +). This species is currently known only from Brazil, without specific location. + + + + \ No newline at end of file diff --git a/data/38/48/82/3848822FFFB71E94606E211EFFA8FD78.xml b/data/38/48/82/3848822FFFB71E94606E211EFFA8FD78.xml new file mode 100644 index 00000000000..d9a86372c0a --- /dev/null +++ b/data/38/48/82/3848822FFFB71E94606E211EFFA8FD78.xml @@ -0,0 +1,296 @@ + + + +Info Flora Schweiz - Cyperaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/cyperaceae.html + +url + + + + + +Eleocharis obtusa +(Willd.) Schult. + + + + + + +Stumpfkoepfige +Sumpfbinse + + + + + +Art ISFS: 145550 Checklist: 1016280 +Cyperaceae +Eleocharis +Eleocharis obtusa (Willd.) Schult. + + + +Bestimmungsschluessel + + + +Zusammenfassung + + + + +Artbeschreibung + +(nach +Lauber & al. 2018 +) + +: Wie + +E. ovata + +, aber bis +60 cm +hoch, mit kurzen unterirdischen +Auslaeufern +. +Staengel +bis +2 mm +dick. +Aehre +8-16 mm +lang. Griffelbasis 0,5-0,8 mm breit, 2/3 bis fast so breit wie die Frucht. + + + +Standort und Verbreitung in der Schweiz TI, VD u.a. + + + +Verbreitung global + +(nach +Lauber & al. 2018 +) + +: Nordamerikanisch + + + + +Oekologische +Zeigerwerte + +(nach +Landolt & al. 2010 +) + +4 + w + 33-453.a-t + + + + + +Oekologie + + + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + +KEINE ANGABE + + +
+
+
+
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F--Lichtzahl L--Salzzeichen--
Reaktionszahl R--Temperaturzahl T--
+Naehrstoffzahl +N +-- +Kontinentalitaetszahl +K +--
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Eleocharis obtusa +(Willd.) Schult. + + + + + + +Volksname Deutscher Name: + +Stumpfkoepfige +Sumpfbinse + +Nom +francais +: + +Eleocharide +obtuse + +, +Scirpe obtus +Nome italiano: +Giunchina ottusa + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Eleocharis obtusa (Willd.) Schult. + + +Checklist 2017 + +145550
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Kommentare aus der +Checklist 2017 +Neues Taxon: +Gegenueber +SISF-2 neu aufgenommener Neophyt. Checklist + + + + +Status Indigenat +: Neophyt: nach der Entdeckung von Amerika in der Region aufgetreten (nach 1500) + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein + + +
+
\ No newline at end of file diff --git a/data/38/49/87/384987DACD00FF9EFF69FC3CFF69FBF7.xml b/data/38/49/87/384987DACD00FF9EFF69FC3CFF69FBF7.xml new file mode 100644 index 00000000000..00a09817b17 --- /dev/null +++ b/data/38/49/87/384987DACD00FF9EFF69FC3CFF69FBF7.xml @@ -0,0 +1,231 @@ + + + +Hymenoptera Tiphiidae from Arabian peninsula + + + +Author + +Boni, M. + +text + + +Linzer biologische Beiträge + + +2011 + +2011-07-25 + + +43 + + +1 + + +337 +361 + + + +journal article +10.5281/zenodo.5324544 +0253-116X +5324544 + + + + + + + +Anthobosca aspilosoma + +nov.sp. + + + + + + + +Holotype +: +Oman += / +Oman +Dhofar +2000 +Wadi Ashawq +(Al Mughsahyl) 11.IX + +190ft + +16°53’88N/ +53°46’31E +leg. +M.Generani +&PL. +Scaramozzino +/, +MSNP +. + + + +Paratype +: +Oman += / +Oman +Dhofar +2000 Wadi Ashawq 11.IX +190ft +16°53’88N/ +53°46’31E +leg. M.Generani &PL.Scaramozzino/, +MSNP +: +Oman += / /, +MSNP +. + + +: +Oman += / +Oman +Dhofar +2000 Wadi Ashawq (Al Mughsahyl) 11.IX +190ft +16°53’88N/ +53°46’31E +leg. M.Generani &PL.Scaramozzino/, +MSNP +. + + +Female. +Holotype +. +Figs 1-9 +. Measurements: body length = 6.5 mm; forewing length = +4 mm +. + + +Wings hyaline. Body colour brown to dark brown, pterostigma and veins included, with blackish +P, +coxae and some shadows on mesosoma. Semitransparent brown are clypeal lamella, mandible, apical disk + +N +1 + +apical border of metameri, 6 +th +tergum, legs. Semitransparent bright brown tegulae. Most of the body, legs included, covered by mR detectable at x40 (stronger on dorsal +P +). very sparse on head and mesosoma. Lateral +P +smooth and shining. + +es +3 + +shagreened without any +p +. 1 +st +and 2 +nd +terga with very sparse small +p +. The remainder of terga and the sterna are sparsely bipunctate. Apical third of 6 +th +tergum free from +p +and bristles. + +Gradulus delimiting platform (friction area) at the base of inner hind tibia complete and closed apically. + +Male. +Figs 10-17 +. Measurements: body length = 6.3 mm; forewing length = 4.1 mm. + + +Black with white spots. Pterostigma is brown. Wings hyaline. White: most of clypeus but a narrow semitransparent stripe along its ventral border, a stripe along inner border of the eye, a small spot on temples and at the base of mandibles, subapical stripe on + +N +1 + +disk, a mid narrow stripe on tegula which is brown basally and transparent apically, humeral plate, foretarsi and most of fore tibia, basal hind tibia and hintarsus. Sparse +p +on head, and mesosoma, +P +and metasoma mostly covered by +mR +with sparse small +p +. 7thtergum roughly +p +. Sharp clear narrow groove on the middle of 1 +st +tergum for half its length. + + +Tyloids well prominent on 4 +th +to 11 +th +flagellomeri. + + +D i s c u s s i o n. Their conspecificity is highly probable. Small species distinct by the absence of any light spot on the female, which has also a closed friction area on hind tibia. +A. suakinensis +(Magretti 1883) (= +A. arabica +TURNER 1910) gets bigger size, has light spotted body and open friction area on hind tibia; the latter is more stout with bent edges in lateral aspect, while in +A. aspilonota +the upper and ventral border are subrectlinear. Moreover +A. suakinensis +shows +p +and bristles on most of 6 +th +tergum and the +CM +is much less elongated. +A. minima +TURNER 1910 shows many light spots, different head, different distance of toruli from eachother and from eyes, + +N +1 + +less narrowed anterorly in dorsal aspect, different platform on hind tibia, +CM +and 6 +th +tergum. The male differs from +A. suakinensis +described as +A. arabica +by +GORBATOVSKY (1987) +in different shape of the head in dorsal aspect, different apical cells of forewing and genitalia. + + +It belong to the group of +A. aspericornis +(BUYSSON 1898) according to +BONI BARTALUCCI (2005) +. + +E c o l o g y. Unknown. +D e r i v a t i o n o m i n i s Fromthe Greek words άσπιλος = spotless and σώμα = body. + + + \ No newline at end of file diff --git a/data/38/49/87/384987DACD01FF9EFF69FB19FE1CFDB2.xml b/data/38/49/87/384987DACD01FF9EFF69FB19FE1CFDB2.xml new file mode 100644 index 00000000000..fbd8e065306 --- /dev/null +++ b/data/38/49/87/384987DACD01FF9EFF69FB19FE1CFDB2.xml @@ -0,0 +1,243 @@ + + + +Hymenoptera Tiphiidae from Arabian peninsula + + + +Author + +Boni, M. + +text + + +Linzer biologische Beiträge + + +2011 + +2011-07-25 + + +43 + + +1 + + +337 +361 + + + +journal article +10.5281/zenodo.5324544 +0253-116X +5324544 + + + + + + + +Poecilotiphia oasicola +BONI +BARTALUCCI 2001 + + + + + + + + + + +Poecilotiphia oasicola +: +Boni Bartalucci (2001: 40 + + +, 42). + + + + + + +Material. +. +Yemen += (64) / +Yemen +Lahj Mal. +trap +A. v. Harten +RMNH’01/: [(1) + +II.2000 + +– (1) + +VIII-2000 + +– (7) + +IX.2000 + +– (9) + +X.2000 + +– (10) + +XI.2000 + +– (12) + +I.2001 + +– (4) + +II.2001 + +– (8) + +III.2001 + +– (7) + +IV.2001 + +– (5) + +V.2001 + +], +RMNH +; (7) + +/ + +Yemen +Lahj + +17.V-15.VI 2001 + +Mal. Trap A. v. Harten +& +A. Sallum +RMNH’01/, +RMNH +; (1) + +/ + +Yemen +Lahj + +1.X-17.XII.2001 + +Mal. Trap A. v. Harten +& +A. Sallum +RMNH’02/, +RMNH +; (1) + +/ + +Yemen +(6007) +Suq +bani +Mansour + +28.VIII-14.IX.2001 + +Mal. +trap +A. v. Harten +RMNH +RMNH’02/; (2) + +/ + +Yemen +(6014) +Ar Rujum + +24.VII-17.IX 2001 + +A.v.. +Harten +RMNH’02 + +/; +RMNH +; (10) / + +Yemen +(6022) +Lahj +VII-IX.2001 +Mal. +trap +A. v. Harten +& +A. Sallum + +; RMNH’02/, +RMNH +; (4) / + +Yemen +(6247) +Lahj + +1.X-17.XII.2001 + +Mal. +trap A. v. +Harten +& A. +Sallum + +; RMNH’02/, +RMNH +; (15) / + +Yemen +(6814) +Lahj +III-V.2002 +Mal. +trap +A. v. Harten +& +A. Sallum + +; RMNH’02/, +RMNH +; (1) / + +Yemen +(7066) +Seyup +, +light trap + +12-14.VIII.2002 + +A. v. Harten +RMNH’02 + +/; +RMNH +. + + + + \ No newline at end of file diff --git a/data/38/49/87/384987DACD04FF9AFF69FC86FCB9FA4A.xml b/data/38/49/87/384987DACD04FF9AFF69FC86FCB9FA4A.xml new file mode 100644 index 00000000000..2a45d6ced94 --- /dev/null +++ b/data/38/49/87/384987DACD04FF9AFF69FC86FCB9FA4A.xml @@ -0,0 +1,191 @@ + + + +Hymenoptera Tiphiidae from Arabian peninsula + + + +Author + +Boni, M. + +text + + +Linzer biologische Beiträge + + +2011 + +2011-07-25 + + +43 + + +1 + + +337 +361 + + + +journal article +10.5281/zenodo.5324544 +0253-116X +5324544 + + + + + + + +Tiphia elachia + +nov.sp. + + + + + + + +Holotype +: +Oman += / +Oman +2000 +Dhofar +Rd. 31N of +Queiroon +17.17’58N 5405’21E + +2500ft + +29.VIII lrg. +F.Strumia +/ /, +MSNP +. + + + +Female. +Holotype +. +Figs 22-27 +. Measurements: body length = 4.0 mm; forewing length = 2.6 mm. + + +Black. Light brown: ventral flagellum, most of mandible, most of fore leg but coax, apical 2/3of 6 +th +tergum, most of mid and hind tarsi, the semitransparent tegulae, + +LaSt +2 + +, pterostigma and veins. + + +Brown: scape, mid clypeus, tip of mandible, some fore tibia, forecoxa, mid and hind legs but tarsi, posterior area of +P +, 1 +st +sternum and shadows on 4 +th +to 6 +th +sterna. + + +Forewing very slightly coloured. Whitish hair throughout. Lower frons and clypeus but lamella with densely packed small +p +. The remainder of frons and vertex with scattered +p +and +iS +many times greater than their diameter, on the mid vertex along cOc there is a +mR +small area. Progena well shagreened. All the remainder of the body but +P +and last 3 sterna shows the same pattern of +p +of the head. + + +Pam +less elongated than in most of members of the genus; aggregate of last three elements only 1.4 times longer than aggregate of three basal ones. + +N +1 + +disk with a weak irregular carina along its fore border. +em3 +weakly shagreened. Lateral and median ridges of areola well expressed and complete. Irregular carina between lateral and posterior areas. Well distinct carina along lateral edge of horizontal area between +spP +and rear border of + +N +3 + +. Horizontal area with few small +p +and +mR +. Posterior area concave without any ridge, completely covered by small +p +, with scattered few greater +p +. Lateral areas and + +es +3 + +indistinct, both completely covered by regular reticulate sculpture like a strong +mR, +made by approached little knobs; very few small wrinkles only at its anterior upper corner. Hind tibia longitudinally keeled on its inner surface with a very narrow sensorial area. Hind basitarsus with a well distinct shallow groove, as long as 2/3 length of the element. Apical 2/3 of pygidium quite smooth and shining, without both +p +and rugulae. + + +N o t e. It looks very like +T. stertia +ALLEN 1975 +( +Holotype +: /Shillong +Assam +, +India +3.IX. +28/ /L.B.parker collector/ / +Holotype + +Tiphia +s-tertia + +H.W. Allen/ (red) /Type N° +74030 +USNM +/!) in having latearal areas of propodeum and metepisternum indistinct and covered by regular reticulate sculpture, unique occurrences within Tiphiini to my knowledge, but is very distinct by the presence of complete carina along fore border of + +N +1 + +disk and especially the groove on hind basal tarsomerus, both absent in the latter. We could infer its conspecificity with + +T. arthroxantha + +from proximity of the provenance areas, but there is no evident proof about that, just as hitherto it is impossible to associate the unique specimen of +T. stertia +with any male (perhaps +T. birganjae +?). + +D e r i v a t i o n o m i n i s.FromtheGreekελάχεια = small. + + + \ No newline at end of file diff --git a/data/38/49/87/384987DACD05FF95FF69FDCBFB88FE4C.xml b/data/38/49/87/384987DACD05FF95FF69FDCBFB88FE4C.xml new file mode 100644 index 00000000000..039df5b5310 --- /dev/null +++ b/data/38/49/87/384987DACD05FF95FF69FDCBFB88FE4C.xml @@ -0,0 +1,654 @@ + + + +Hymenoptera Tiphiidae from Arabian peninsula + + + +Author + +Boni, M. + +text + + +Linzer biologische Beiträge + + +2011 + +2011-07-25 + + +43 + + +1 + + +337 +361 + + + +journal article +10.5281/zenodo.5324544 +0253-116X +5324544 + + + + + + + +Tiphia sabaea + +nov.sp. + + + + + + + +Holotype +Yemen += / +Yemen +(5960) +12 km +NW +Manakhah + +3.VII-21.VII.2001 + +Mal. +tr. +A. v. Harten +RMNH02 +/, +RMNH +. + + + + +Paratypes +: +Yemen += (5)/ +Yemen +(5960) + +12 km +NW Manakhah + + +3.VII-21.VII.2001 + +Mal. +tr. +A. v. Harten +RMNH02 +/, (4) +RMNH +, (1) +MZUF +; (1) + +/ + +Yemen +(6007) + +12 km +NW Manakhah + + +28.VIIi-14.XI.2001 + +Mal. +tr. +A. v. Harten +RMNH02 +/, +RMNH +; (1) + +/ + +Yemen +(6279) + +12 km +NW Manakhah + + +14.IX- 28.XII.2001 + +Mal. +tr. +A. v. Harten +RMNH02 +/, +RMNH +; (1) + +/ + +Yemen +(7547) + +12 km +NW Manakhah + + +1.I-7.V.2003 + +Mal. +tr. +A. v. Harten +RMNH03 +/, +RMNH +; (4) + +/ + +Yemen +(8100) + +12 km +NW Manakhah + + +15.IX-22.X.2003 + +Mal. +tr. +A. v. Harten +RMNH03 +/, +RMNH + +. + + +: + +Yemen += (44) / +Yemen +(5960) + +12 km +NW Manakhah + + +3.VII-21.VII.2001 + +Mal. +tr. +A. v. Harten +RMNH02 +/, (41) +RMNH +:, (5) +MZUF +; (11) + +/ + +Yemen +(7895) + +12 km +NW Manakhah + + +24.VI- 4.VIII.2003 + +Mal. +tr. +A. v. Harten +RMNH03 +/, (10) +RMNH +, (1) +MZUF +; (4) + +/ + +Yemen +(5841) + +12 km +NW Manakhah + + +9.IV-5.VI.2001 + +Mal. +tr. +A. v. Harten +RMNH02 +/, +RMNH +; (3) + +/ + +Yemen +(6007) + +12 km +NW Manakhah + + +28.VIIi-14.XI.2001 + +Mal. +tr. +A. v. Harten +RMNH02 +/, +RMNH +; (2) + +/ + +Yemen +(6279) + +12 km +NW Manakhah + + +14.IX– 28.XII.2001 + +Mal. +tr. +A. v. Harten +RMNH02 +/, +RMNH +; (7) + +/ + +Yemen +(7547) + +12 km +NW Manakhah + + +1.I-7.V.2003 + +Mal. +tr. +A. v. Harten +RMNH03 +/, +RMNH +; (2) + +/ + +Yemen +(7585) + +12 km +NW Manakhah + + +15.V-23.VI.2003 + +Mal. +tr. +A. v. Harten +RMNH03 +/, +RMNH +; (5) + +/ + +Yemen +(8100) + +12 km +NW Manakhah + + +15.IX-22.X.2003 + +Mal. +tr. +A. v. Harten +RMNH03 +/, (4) +RMNH +, (1) +MZUF +; (1) + +/ + +Yemen +(8117) + +12 km +NW Manakhah + + +15.IX-22.X.2003 + +Mal. +tr. +A. v. Harten +RMNH03 +/, +RMNH + +. + + +Male. +Holotype +. +Figs 28-35 +. Measurements: body length = 6.5 mm; forewing length = + +4.0 mm. Black. Brown: eye, upper scape,,upperside of flagellum from 2nd to the final element, +pterostigma, the semitransparent veins, hind trochanter and most of hind femur. Veins are sbrown. Light reddish brown: lamella of clypeus, basal mandible, apex of scape, pedicel, basal flagellomerus and ventral side of the remainder ones, fore and mid legs but coxae, apex of hind femur, hind tibia and hind tarsus, the semitransparent tegula. + +Clypeus with small +p +and +iS +as large as their diameter. Lower frons densely +p +, almost finely sculptured, the remainder with +p +progressively more scattered toward ocelli, where pitless areas larger than ocelli exist. Vertex, with +iS +larger than +p +; along +cOc +there is a stripe with well detectable +mR +. Genae lack any +mR +with +p +becoming progressively denser (with +iS +very smaller than their diameter) toward +PoG +. On the lower genae there are strong buttressing ridges perpendicular to +cOc +. Progena completely shagreened. Mandible without any denticle along inner edge. 3 +rd +element of +Pam +with apical forward projection. + + + +N +1 + +disk with a well produced carina along ist foreborder with sparse not well distinct buttressing ridges; lateral surface completely transversally shagreened with a deeper groove on ist ventral portion; +p +on the disk well spaced with smaller +p +on the + +iS. Sc +1 + +with densely packed +p +on its middle. + +Sc +21 + +irregularly +p +. Small +p +on postscutellar area of + +N +3 + +. + +es +1 + +with regularly spaced small +p +with +iS +shorter than their diameter. + +es +2 + +: well expressed omaulus and regularly spaced +p +on mid and ventral surface ( +iS +as large or shorter than their diameter) with weak (detectable only at x50) +mR +on ist ventral surface and + +LaSt +2 + +. + +em +3 + +finely shagreened. Fore coxa irregularly +p +, mid coxa with densely and regularly packed, hindcoxa with dense greater +p +. Lateral ribs of areola well prominent, the mid one only expressed on its basal half. Surface of horizontal area without +p +and irregularly shagreened and or sculptured. Posterior area without any vertical ridge. Lateral areas with more than 30 wrinkles, mostly incomplete. + + +1 +st +tergum almost +p +-ess but subapical stripe. 2 +nd +tergum with scattered +p. +3 +rd +to 7 +th +terga with more densely packed +p +and +mR +(detectable at x30) covering +iS. +1 +st +sternum irregularly +p +, while 2 +nd +to 6 +th +sterna are similar to terga. +mR +on last metameri. Tuberculum on 5th sternum with an orifice lying under its uplifted edge. + + +Female. Measurements: body length = 10.5 mm; forewing length = +6 mm +. + + +Black. Brown: Tip of coxae "fore trochanter and mid and hind femurs; anterior surface of fore femur; pterostigma and tegulae; the semitransparent apical border of + +N +1 + +disk, + +LaSt +2 + +, distal half of pygidium. Reddish light brown: mandibles, antennae, clypeal lamella. Forewing slightlydarkened. + + +Apart clypeus and lower frons (densely p like in all the members of the subfamily) the remainder of the head shows irregular +p +and +iS +mostly larger than their diameter with only a stripe of denser +p +along +cOc +. +p +on disk of + +N +1 + +, + +Sc +1 + +, + +Sc +2 +, + +es +1 +, most of + +es +2 + +and coxae like on the head. Lateral + +N +1 + +finely transversally shagreened with a distinct oblique groove. 1 +st +tergum almost pitless but a subapical densely +p +stripe; 2 +nd +tergum medially pitless, laterally like head; 1 +st +sternum with small scattered +p +; +p +on 2 +nd +to 5 +th +sterna like on head; 6 +th +sternum more densely +p +. +P +with irregular +mR +on surface besides areola; surface inside areola irregularly weakly wrinkled; lateral surface wrinkled: posterior surface concave, finely and densely sculptured throughout, with a trace of ridge on ist basal half. + + +Frons without any vertical median ridge. Progena shining and pitless. Genal bridge well expreesed with contiguous genal areas sunken compared to the remainder upper ones. 3rd element of +Pam +with apical forward extension. Weak and complete distinct keel along fore border of + +N +1 + +disk. Colpus on + +Sc +1 + +not connected to parapsidal lines. Hind tibia with narrow sensorium and distinct longitudinal keel on ist inner surface with +mR +under it. Hind basal tarsomerus without groove. + + +N o t e. Variability occurs only in size, from 5 to 6.5 mm. Female run to the item of + +Tiphia +cinchonae + + +ALLEN +1975 + +in his monography on + +Tiphia + +of the Indian subcontinent; the male shares with male of +T. cinchonae +the shape of 3 +rd +element of +Pam +. Nevertheless the female here described show the same extension on 3 +rd +Pam +like the male, while the female +paratype +of +T. cinchonae +(same label of the +paratype +male here recorded) does not possess it. Moreover this male has a deep orifice beneath tuberculum on 5 +th +sternum, absent in +T. cinchonae +. Other differences from Allen’s type are different shape of the basal elements of +Pam +, the shape of the head and clypeus in frontal aspect, of +N + + +1 + +in + +dorsal aspect and genitalia. The female differs also in lighter foreleg and presence of a ridge on the posterior area of propodeum. The here described males show brighter legs and antennae than +T. cinchonae +. + +E c o l o g y. Unknown. + +D e r i v a t i o n o m i n i s. From sabaeus = inhabitant of ancient kingdom of +Saba +. + + + + \ No newline at end of file diff --git a/data/38/49/87/384987DACD06FF99FF69FF43FCB0FC25.xml b/data/38/49/87/384987DACD06FF99FF69FF43FCB0FC25.xml new file mode 100644 index 00000000000..54e83f72049 --- /dev/null +++ b/data/38/49/87/384987DACD06FF99FF69FF43FCB0FC25.xml @@ -0,0 +1,154 @@ + + + +Hymenoptera Tiphiidae from Arabian peninsula + + + +Author + +Boni, M. + +text + + +Linzer biologische Beiträge + + +2011 + +2011-07-25 + + +43 + + +1 + + +337 +361 + + + +journal article +10.5281/zenodo.5324544 +0253-116X +5324544 + + + + + + + +Poecilotiphia nitens + +nov.sp. + + + + + + + +Holotype +: +Yemen += / +Yemen +(8222) +12 km +NW +Manakhah +mal. Trap. + +22.X-3.XII.2003 + +A. v. Harten +RMNH03 +/, +RMNH +. + + + +Female. +Holotype +. +Figs 18-21 +. Measurements: body length = +10 mm +; forewing length = +5 mm +. + + +General aspect shining. Head (but clypeus), forecoxa and mesosoma (but + +LaSt +2 + +) black. Tip of +Tsa +, clypeus, scape and flagellum, mandible, mid and hind legs, tegulae, pterostigma and veins are light brown. Fore leg, most of 1 +st +metamerus but narrow apical stripe on tergum, basal half of 2 +nd +tergum are brown. The remainder of metasoma is bright ferruginous. Yellowish hair on the scape, whitish elsewhere. +Pal +3– and +Pam +4– segmented. + +N +1 + +disk wider than high (ratio LA/A about 1.4). Dorsal +P +with a distinct long median longitudinal groove, somewhat irregular, shaped initially by three elongated +p +followed by a narrow stripe of very small p groove. + + +N o t e. Well distinct species by the enamelled aspect, shape of the head, large basal +Pal, +large pterostigma, long propodeal groove. All the + +Poecilotiphia + +males in so far recorded from Arabian peninsula, +P. lacteipennis +E.SAUNDERS 1901, +P. scorteccii +GUIGLIA 1968, +P. collarinata +BONI BARTALUCCI 1997, + +P. oasicola +BONI BARTALUCCI 2001 + +and +P. dhofarensis +BONI BARTALUCCI 2004 belong to the +P. albomaculata +group ( +BONI BARTALUCCI 2004a +), whose hitherto known females (about 15) show a longer than wide pronotal disk. Excluding +lacteipennis +, whose female is known, and +oasicola +(which otherwise is very common in +Yemen +) since on records from Saharian oasis its female appears to be different, it is impossible to couple it with no one of these taxa and at the same time to exclude the existence of further undescribed male belonging to the +nigripes +group whose the hitherto known +four females +show the pronotum larger than high in dorsal aspect like the present specimen. Future data could clear the situation. + +Male. Unknown. +E c o l o g y. Unknown. +D e r i v a t i o n n o m i n i s. From Latin nitens = shining. + + + \ No newline at end of file diff --git a/data/38/49/87/384987DACD09FF90FF69FCD8FD76F9DF.xml b/data/38/49/87/384987DACD09FF90FF69FCD8FD76F9DF.xml new file mode 100644 index 00000000000..80e9ebbd962 --- /dev/null +++ b/data/38/49/87/384987DACD09FF90FF69FCD8FD76F9DF.xml @@ -0,0 +1,457 @@ + + + +Hymenoptera Tiphiidae from Arabian peninsula + + + +Author + +Boni, M. + +text + + +Linzer biologische Beiträge + + +2011 + +2011-07-25 + + +43 + + +1 + + +337 +361 + + + +journal article +10.5281/zenodo.5324544 +0253-116X +5324544 + + + + + + + +Pseudotiphia +( +Pseudotiphia +) +inopinata + +nov.sp. + + + + + + + +Holotype +: +Yemen += / +Yemen +(5960) +12 km +NW +Manakhah + +3.VII-21.VII.2001 + +Mal. +tr. +A. v. Harten +RMNH02 +/, +RMNH +. + + + + +Paratype +: +Yemen += (2) / +Yemen +(7585) +12 km +NW +Manakhah + +15.V-23.VI.2003 + +Mal. +tr. +A. v. Harten +RMNH02 +/, (1) +RMNH +, (1) +MZUF +; (1) + +/ + +Yemen +(8100) +12 km +NW +Manakhah + +15.IX- 22.X.2003 + +Mal. +tr. +A. v. Harten +RMNH03 +/, +RMNH + +. + + + +Paratype +: +Yemen += (27) / +Yemen +(5960) +12 km +NW +Manakhah + +3.VII-21.VII.2001 + +Mal. +tr. +A. v. Harten +RMNH02 +/, +RMNH +: (25), +MZUF +: (2); (1) + +/ + +Yemen +Lahj Mal.tr. N.5588/89/90 +A. v. Harten +& A. SAllam, RMNH’01/, +RMNH +; (2) + +/ + +Yemen +(7895) +12 km +NW +Manakhah + +24.VI- 4.VIII.2003 + +Mal. +tr. +A. v. Harten +RMNH03 +/, +RMNH + +. + + +Female. +Holotype +. +Figs 53-56 +. Measurements: body length = 10.5 mm; forewing length = 6.5 mm. + + +Black. Brown are: upper side of flagellum, pterostigma and veins, most of legs but coxae. Reddish brown are lamella of clypeus, scape, pedicel and 1 +st +flagellomerus, shadows on legs, apical half of 6 +th +tergum. Ventral side of flagellum is light brown. Forewing shaded. + + +Clypeal surface covered by dense small +p +bearing very weak bristles. Largely spaced +p +, with +iS +larger than their diameter, on the remainder of head, with a stripe of small +p +on vertex along +cOc +. The same +p +on + +N +1 + +disk with no carina along its foreborder; lateral + +N +1 + +with transversal weak wrinkles progressively strengthening toward posteroventral corner; dark apical border. Fore + +Sc +1 + +without any gradulus. + +Sc +2 + +looks like in +T. villosa +, but presence of omaulus expressed only medially wearing out upperly and ventrally. + +es +1 + +bipunctate by small +p +among scattered larger ones. + +es +2 + +with +p +like head and with stripe of small +p +along the median suture; omaulus well expressed only on the upper side. + +em +3 + +largely smooth and shining. + +es +3 + +weakly shagreened with scattered small +p +. Sensorial areas of hind tibia surrounded by shining pitless belt; sensorial area of mid tibia strongly transversal; both of them are flushed with surrounding surface. No groove on hind basal tarsomerus. Lateral ridges of areola well produced and broadly sinuous, the mid one is irregular and weaker. Posterior surface concave and without any trace of ridge. Lateral P with about 30 transversal wrinkles. + + +1 +st +tergum with very scattered +p +and strong gradulus along the border between vertical and horizontal surfaces. Weak buttressing ridges along colpus of 2 +nd +tergum. 2 +nd +to 5 +th +terga with irregularly spaced +p +. Apical third of 6 +th +tergum (pygidium) with only very weak traces of longitudinal rugulae. 1 +st +sternal surface with regularly spaced snmall +p +throughout. +p +of 2 +nd +sternum like terga. 3 +rd +to 6 +th +sterna covered by well detectable at x25 +mR +, with scattered small +p +progressively becoming denser toward 6 +th +element. + + +Male. +Figs 51 +, +57-63 +.Measurements: body length = 6.5 mm; forewing length = 4.5 mm. + + +Black. Brown: tip of mandible, lateral clypeus, pterostigma, upper fore femur, most of mid and hind femur, tip of tegulae, upper hind tibia and most of hind tarsus, tip of 6 +th +sternum, apex of trochanters; the semitransparent veins and tip of + +LaSt +2 + +. Light brown: most of mandible, ventral surface of scape, upper flagellum, central clypeus and lamella, fore trochanter, outer fore tibia, fore and mid tarsi, ventral femurs. Ventral flagellum is lighter brown-yellow. + + +Clypeus and lower frons like in +T. villosa +; +p +progressively more scattered from lower frons to vertex, where there are pit less areas around ocelli and +iS +larger than their diameter; stripe of small +p +along +cOc +. Progena irregularly shagreened; no additional denticle on mandible. Near genal bridge areas the +cOc +shows a ventral lamellar projection. Palpi far longer than +FoO +. + + +Sparse +p +on mid + +N +1 + +disk, denser +p +on its fore surface with small +p +among them; lateral + +N +1 + +shagreened without any groove; laminated carina along ist fore border. Omaulus well produced. + +es +1 + +with few large +p +anteriorly, posterior and inner surface shagreened with few small +p +; Lateral + +es +2 + +bipunctate till signum. Ventral forecoxa bipunctate, mid coax covered by small +p +, hindcoxa densely +p +at its base then sparser apically. +P +: well produced lateral ridges of areola; mid ridge of areola less prominent and worn out at its middle; horizontal area irregularly shagreened; posterior surface concave without ridge; about 20 strong complete wrinkles, alternated to about 10 incomplete. + +em +3 + +mostly smooth with +p +along the border with + +es +2 + +; + +es +3 + +weakly and irregularly shagreened with strong buttressing ridges along its border with + +em +3 + +. Sensorial area of hind tibia as narrow as in other taxa of the genus, surrounded by shining belt; sensorial area of mid tibia not well distinct, detectable by smooth and shining surface; both of them flushed with surrounding surface. The +CM +on the fore wings of the males just a bit more extended apically than 2 +nd +CSM +. + + +Distal border of metameri black ( +Fig. 51 +) (not at all semitransparent like in other taxa of the genus) with a narrow distinct groove worn out on their middle portion and becoming progressively delimited to the lateral corner in the last ones. Strong gradulus dividing horizontal from vertical surfaces of 1 +st +tergum, with sparse +p +throughout and a stripe of small +p +on the middle of latter; well prominent buttressing ridges of colpus on 2 +nd +tergum. +p +progressively denser from 2 +nd +to 7 +th +terga. 1 +st +sternum with strong lateral grooves joining to the subapical transversal groove, which has strong buttressing ridges. 2 +nd +sternum with sparse +p +. 3 +rd +to 5 +th +sterna with few small +p +but an aical stripe of greater +p +and covered throughout by well detectable at x20 +mR. +Short and stout medially prominent tuberculum on 5 +th +sternum. Basal 6 +th +sternum with +mR +and densely +p +. + + +Note. Well known taxon from other taxa of the genus by the lack of groove on hind basitarsus in females, the ventral extension of +cOc +, apically more extended +CM +and particular distal border of metameri in males compared to +villosa +( +Fig.52 +, by a male from +Italy +: / + +Dint Genova +V 1940 +Franciscolo + +/). to whose group they belong. Therefore its position in the key of taxa of the genus ( +BONI BARTALUCCI 2010 +) could be at the items 4 and 16 for the females and males respectively. + +E c o l o g y. Unknown. +D e r i v a t i o n o m i n i s. Inopinata = unexpected. + + + \ No newline at end of file diff --git a/data/38/49/87/384987DACD0BFF94FF69FF43FECAFD5E.xml b/data/38/49/87/384987DACD0BFF94FF69FF43FECAFD5E.xml new file mode 100644 index 00000000000..245dd872999 --- /dev/null +++ b/data/38/49/87/384987DACD0BFF94FF69FF43FECAFD5E.xml @@ -0,0 +1,235 @@ + + + +Hymenoptera Tiphiidae from Arabian peninsula + + + +Author + +Boni, M. + +text + + +Linzer biologische Beiträge + + +2011 + +2011-07-25 + + +43 + + +1 + + +337 +361 + + + +journal article +10.5281/zenodo.5324544 +0253-116X +5324544 + + + + + + + +Tiphia +( +Tiphia +) +arthroxantha + +nov.sp. + + + + + + + +Holotype +Yemen += / +Yemen +(5960) +12 km +NW +Manakhah + +3.VII-21.VII.2001 + +Mal. +tr. +A. v. Harten +RMNH02 +/, +RMNH +. + + + +Paratype +Yemen += (2) / +Yemen +(5960) +12 km +NW Manakhah +3.VII-21.VII.2001 +Mal.tr. A. v. Harten +RMNH +02/, +RMNH +. + + +Male. +Holotype +. +Figs 38-45 +. Measurements: body length = 5.3 mm; forewing length = +3,6 mm +. + + +Black. Reddishs-yellow: the whole antennae, mid clypeal disk, mandibles, semitransparent tegulae, semitransparent veins, all the legs but coxae, Tip of 7 +th +tergum and 6 +th +sternum. Tip of mandibles and pterostigma are brown. + + +Head with very sparse +p +on frons and vertex with large impunctate areas around ocelli and stripe with +mR +and small +p +along +cOc +. No subapical denticle on mandible. Tyloids well expressed and prominent on all the flagellomeri. + + +p +on most of mesosoma like on head. + +N +1 + +disk with a distinct laminated carina along the fore border and a semitransparent impunctate apical stripe; lateral + +N +1 + +shagreened uppermost with a median transversal strong groove and wrinkled downwards. + +N +3 + +with only few small +p +. + +es +1 + +with denser smaller +p +and +mR +. Omaulus well distinct till signum.; ventral + +es +2 + +with a stripe of small +p +along the median suture. + +em +3 + +finely wrinkled uppermost and smooth ventrally. + +es +3 + +shagreened. Horizontal +P +shagreened outside areola, roughly transversally wrinkled inside; posterior (vertical) area irregularly corrugated; lateral areas with irregularly spaced strong wrinkles; well prominent lateral ribs of areola (mid one weaker). Inner hind coxa rounded. + + +1 +st +to 6 +th +terga and 2 +nd +to 5 +th +sterna with sparse +p +; 7 +th +tergum and 6 +th +sternum deeply and more densely +p +; 1 +st +sternum with large deep +p +at the base of the disk, apically with a strong transversal groove and buttressing ridges along it. + + +N o t e. +Paratypes +do not show differences apart the smaller size of one of them (less than +5 mm +). In ALLEN’ s key (1975) it runs to the item of +T. birganjae +[ +Holotype +: / +Nepal +nr Birganj Lothar +450ft +Malaise trap n° 30 Can. +Nepal +Exp./ / +Holotype + +Tiphia +birganjae + +HW Allen/ / +Holotype +Tiphia +birganjae +CNC +N.15563/, +CNC +!] to which it looks very like. The latter shows different shape of the head in dorsal (more transversal) and frontal aspect (with a more depressed vertex), shape of clypeal disk (less prominent ventrally in frontal aspect and with a median notch), shape of + +N +1 + +disk in dorsal aspect (with stronger carina and buttressing ridges), a strong longitudinal carina on the inner surface of hind coxa, different and less prominent tubercle on 5 +th +sternum, different genitalia. + +Female. Unknown. +E c o l o g y. Unknown. +D e r i v a t i o n n o m i n i s From the Greek words: άρθρον = limb; ξανθός = reddish yellow. + + + \ No newline at end of file diff --git a/data/38/49/87/384987DACD0BFF97FF69FAC0FE41FC76.xml b/data/38/49/87/384987DACD0BFF97FF69FAC0FE41FC76.xml new file mode 100644 index 00000000000..7684fa0411c --- /dev/null +++ b/data/38/49/87/384987DACD0BFF97FF69FAC0FE41FC76.xml @@ -0,0 +1,193 @@ + + + +Hymenoptera Tiphiidae from Arabian peninsula + + + +Author + +Boni, M. + +text + + +Linzer biologische Beiträge + + +2011 + +2011-07-25 + + +43 + + +1 + + +337 +361 + + + +journal article +10.5281/zenodo.5324544 +0253-116X +5324544 + + + + + + + +Tiphia +( +Tiphia +) +eremopolites + +nov.sp. + + + + + + + +Holotype +: +Oman += / +Oman +2000 +Dhofar +Rd. 31N of +Queiroon +17.17’58N 5405’21E + +2500ft + +29.VIII lrg. +F.Strumia +/ /, +MSNP +. + + + +Female. +Holotype +. +Figs 46-50 +. Measurements: body length =.9.0 mm; forewing length = 5.5 mm. + +Black. Apex of scape, flagellum and mandibles are reddish brown. Brown: pterostigma, tibiae and tarsi, semitransparent apical tegulae and veins. Apical third of 6th tergun is light brown. Forewing darkened. + +Progena smooth with few +p +along +FoO +. Vertex with a shagreened stripe along +cOc +. Very scattered +p +on the remainder of head. Same pattern of +p +on + +N +1 + +disk, + +Sc +1 + +, + +Sc +2 + +, and + +es +2 + +. Distinct, very low irregular carina along fore border of + +N +1 + +disk. Lateral + +N +1 + +shagreened throughout with a shallow median transverse groove and few wrinkles on its down third. Gradulus on fore + +Sc +1 + +connnected to parapsidal lines. Omaulus well expressed till signum. Em3 shagreened throughout, more impressed uppermost. Tegulae very long almost reaching back border of + +Sc +2 + +. + +es +3 + +shagreened. Inner surface of hind tibia distinctly keeled with a narrow, flushed with surrounding area, sensorium. Short and shallow groove on hind basitarsus. Horizontal surface of +P +slightly sculptured and +p +with large smooth areas; areola with narrow moderately prominent lateral and broader lower median ridges; posterior area concave with small regularly packed +p +throughout; lateral areas with strong complete wrinkles. + + +Terga and 2 +nd +to 6 +th +sterna with sparse p progressively becoming denser toward apical element. 1 +st +tergum with a subapical stripe of p and a distinct unbroken small groove between it and the edge. Analogous groove present also on 2 +nd +to 5 +th +terga but often interrupted. Apical third of 6 +th +tergum smooth with obscure traces of broad costulae. 1 +st +sternal disk with lateral groove and sparse small +p +. Faible +mR +on 3 +rd +to 5 +th +sterna, stronger on 6 +th +one. + +Male. Unknown. + +N o t e.IntheALLEN’ s key (1975) it runs to +T. tegelonga +, which is well known because of different head and clypeal disk in frontal aspect, pronotal disk in dorsal aspect with absence of carina along its fore border, not connected gradulus to parapsidal lines on + +Sc +1 + +, smaller pterostigma and sub rounded sensorium on hind tibia. + +E c o l o g y. Unknown. +D e r i v a t i o n o m i n i s From the Greek ερημοπολίτης = inhabitant of desert, because of provenance area. + + + \ No newline at end of file diff --git a/data/38/49/87/384987DACD0FFF92FF69FC1FFD41FA54.xml b/data/38/49/87/384987DACD0FFF92FF69FC1FFD41FA54.xml new file mode 100644 index 00000000000..6bd44c2da43 --- /dev/null +++ b/data/38/49/87/384987DACD0FFF92FF69FC1FFD41FA54.xml @@ -0,0 +1,389 @@ + + + +Hymenoptera Tiphiidae from Arabian peninsula + + + +Author + +Boni, M. + +text + + +Linzer biologische Beiträge + + +2011 + +2011-07-25 + + +43 + + +1 + + +337 +361 + + + +journal article +10.5281/zenodo.5324544 +0253-116X +5324544 + + + + + + + +Pseudotiphia +( +Acanthotiphia +) +mira + +nov.sp. + + + + + + + +Holotype +: +Yemen += / +Yemen +(7585) +12 km +NW +Manakhah + +15.V-23.VI.2003 + +Mal. +tr. +A. v. Harten +RMNH03 +/, +RMNH +; + + + + +Paratype +: +Yemen += / +Yemen +(7547) +12 km +NW +Manakhah + +1.I-7.V.2003 + +Mal. +tr. +A. v. Harten +RMNH03 +/, +RMNH + +; + + +Paratype +: +Oman += / +Oman +Dhofar +2000 Rd 31 Queiroo Heiritti dint. +2500 ft +27.VIII +17°17’58N +/ +54°05’21E +M.Generani &/ + + +Male. +Holotype +. +Figs 68-74 +. Measurements: body length = 5.4 mm; forewing length = +3,7 mm +. + + +Black. Brown: antennae (with brighter ventral side), mandibles, tegulae, legs but coxae, apex of 6 +th +sternum. + + +Apart clypeus and lower frons (similar to the general pattern of + +Tiphia + +) the head shows sparse small +p +with large smooth areas except on vertex along +cOc +and on ventral genae along lateral extension of +cHy +, where denser +p +and fine shagreened sculpture exist. Progena smooth and shining. +PoG +ridged, its area sunken compared to the remainder of genae. Ventral +cOc +slightly prominent and laminated. Mandible with a subapical small tooth. + + +Mesosoma mostly with sparse +p +too. Distinct but very low carina along foreborder of + +N +1 + +, with very short almost undetectable buttressing ridges. Lateral + +N +1 + +smooth uppermost with rough +p +anteriorly, ventrally with few strong transversal wrinkles; + +N +1 + +disk with black opaque apical stripe. Omaulus well expressed till signum. + +es +2 + +with irregularly spaced +p +. Finely wrinkled + +em +3 + +uppermost, smooth ventrally. Horizontal surface of +P +outside areola shagreened anteriorly with few +p +, wrinkled on its posterolateral corner and with finely irregular surface inside areola; posterior surface concave, without any ridge and with concentric rough sculpture and +p +. Well prominent ridges on sides of areola with weaker and incomplete median one; lateral P with strong wrinkles (about 15) invading es +3 +becoming weaker. Sensorium on hind tibia very narrow and somehow hardly distinct from surrounding large oranged area and flushed with it. On apical mid tibia there is a large smooth subrounded area not easily recognizable as sensorial area. Basal hind tarsomerus without any groove and with sparse whitish bristles on its upper and outer surfaces. + + +Black border of metameri with very narrow membranaceous edge. Sparse +p +on 2 +nd +to 6 +th +terga, 2 +nd +to 5 +th +sterna except their base where there is a stripe of denser +p +; 1 +st +tergum with very sparse +p +, large sensorial area and a low irregular gradulus between vertical and horizontal surfaces; 7 +th +tergum and 6 +th +tergum more densely +p t +hroughout; 1 +st +sternum with lateral broad ridges flanked by shallow groove on the disk; rough irregular trace of gradulus on 2 +nd +sternum; 6 +th +sternum with a large median stripe prominent on the surrounding surface; long horn, far trespassing apical border of the element, on subapical side of 2 +nd +tergum; very shorter horns, not trespassing apical edges, on 3 +rd +to 5 +th +sterna. + + +Female. +Figs 75-79 +. Measurements: body length = 5.9 mm. + + +Black. Brown: clypeal lamella, scape, mandible tip, legs with lighter shadows, apex of 6 +th +sternum. Flagellum (a bit darker upperside), mandible, semitransparent + +LaSt +2 + +, tegula, veins, pterostigma and apical half of 6 +th +tergum are light brown. + + +Most of the head with quite deep sparse +p +and large impunctate areas on the frons and vertex. Section of +cOc +near +PoG +moderately dilated ventrally. Progena with weak +mR +. Quite prominent ventral projection of the clypeal lamella in frontal aspect. All the flagellomeri (but last) clearly thicker than long. +p +on + +N +1 + +disk, + +es +1 + +, and + +es +2 + +like on the head. Irregular, low, worn out medially carina along its fore border; its lateral area without any gradulus neither groove, with +mR +on its upper half and weakly wrinkled ventrally. + +Sc +1 + +without neither colpus neither gradulus along its fore border, just with a sub triangular +p +- less area delimited by large +p +which are present on its middle area and laerally along +sup +. + +Sc +2 + +with sparse large +p +, postscutellar area only with sparse very minute +p +. + +es +2 + +with ow,well expressed till signum omaulus. + +em +3 + +covered by strong +mR +. + +es +3 + +finely shagreened uppermost,smooth ventrally. Ventral coxae with very sparse +p +. Mid tibia with very small ovoid sensorium hardly detectable under incident light surrounded by shining area. Inner surface of hind tibia well keeled longitudinally. Basal hind tarsomerus with a strong long groove. Horizontal area of Propodeum finely sculptured and/or +mR +throughout. Areola subtrapezoidal, clearly tapering backward and with regular straight ribs; the mid one stops just a bit before posterior carina; area around +spP +delimited by regular rib subparallel to lateral carina and getting + +N +3 + +. Posterior area concave, without any median ridge and completely covered by sculpture formed by densely approached shallow p. lateral areas with weak wrinkles, sub longitudinal (with +mR +among them) on its fore half and sub vertical backward. +p +on 1 +st +sternal surface like on the head on the disk, regular and very small trhoughout the vertical portion; irregular by strong +p +subapical row; sensorial area on the sides very large and haired, delimited from disk by an acutely angled edge. 2 +nd +to 5 +th +terga and 2 +nd +to 5 +th +sterna with large semicircular, shallow and sparse +p +. Subapical stripe of smaller p well distinct only on 2 +nd +tergum. Smooth apical half of 6 +th +tergum. 1 +st +sternal disk flattened and mostly smooth with rare small p and long lateral furrow. 6 +th +sternum with regularly packed rounded +p +. + + +Note. +Holotype +lacks right mid tarsomerus. Male +paratype +is in poor condition lacking the entire head, pronotum, propleurae and fore legs. Female +paratype +lacks most of left flagellum. Both of them show character states identifying members of the genus + +Pseudotiphia + +(no colpus along for border of +Sc + + +1 + +in + +females, sensorium on mid tibia of both sexes, no differentiated long brisltle on the palette of gonosquama) from members of + +Tiphia + +. + + +Their conspecificity is proposed because both of them show a moderate ventral extension of +cOc +, very small and almost indistinct sensorium on mid tibiae and proximity of the provenance areas; the male shows peculiar additive character states whereas the female do not show differences from other females of the genus, apart the quite prominent ventral projection of the clypeal lamella in frontal aspect (in other female + +Pseudotiphia + +the clypeal lamella is poorly exceeding clypeal sides in frontal aspect). Therefore there is no certainty about and it needs further confirmation. + + + + \ No newline at end of file diff --git a/data/38/4A/2E/384A2E04013995C94CB2F9F2053C4DE1.xml b/data/38/4A/2E/384A2E04013995C94CB2F9F2053C4DE1.xml new file mode 100644 index 00000000000..d10362859d2 --- /dev/null +++ b/data/38/4A/2E/384A2E04013995C94CB2F9F2053C4DE1.xml @@ -0,0 +1,156 @@ + + + +Order Chiroptera - Family Phyllostomidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +395 +426 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Phyllonycteris +Gundlach 1860 + + + + + + + +Phyllonycteris +Gundlach 1860 + +, +Monatsb. K. Preuss. Akad. Wiss. Berlin, 1860: 817 + +. + + + + +Type Species: + +Phyllonycteris poeyi +Gundlach 1861 + + + + + +Synonyms: + +Rhithronycteris +Elliot 1904 + +. + + + + +Species and subspecies: +3 species with 2 subspecies in 2 subgenera: + + +Subgenus + +Phyllonycteris (Phyllonycteris) +Gundlach 1860 + + + +Subgenus + +Phyllonycteris (Reithronycteris) +Miller 1898 + + + +Species + +Phyllonycteris (Reithronycteris) aphylla +Miller 1898 + + + +Species + +Phyllonycteris (Phyllonycteris) major +Anthony 1917 + + + +Species + +Phyllonycteris (Phyllonycteris) poeyi +Gundlach 1860 + + + +Subspecies + +Phyllonycteris (Phyllonycteris) poeyi +subsp. +poeyi +Gundlach 1860 + + + +Subspecies + +Phyllonycteris (Phyllonycteris) poeyi +subsp. +obtusa +Miller 1929 + + + + + +Discussion: +Two subgenera are recognized, + +Phyllonycteris + +and + +Reithronycteris + +. + + + + \ No newline at end of file diff --git a/data/38/4A/AE/384AAE1CFF94CC295D8EFB16FCF832AD.xml b/data/38/4A/AE/384AAE1CFF94CC295D8EFB16FCF832AD.xml new file mode 100644 index 00000000000..db239675a3c --- /dev/null +++ b/data/38/4A/AE/384AAE1CFF94CC295D8EFB16FCF832AD.xml @@ -0,0 +1,267 @@ + + + +New leptestherid clam shrimps (Pancrustacea: Branchiopoda: Spinicaudata Leptestheriidae) from peninsular India + + + +Author + +Padhye, Sameer M. +Biologia Life Science LLP, Ahmednagar, India. + + + +Author + +Kulkarni, Mihir R. +Laboratory for Conservation of Endangered Species, CSIR-CCMB, Hyderabad, Telangana, India. + + + +Author + +Pagni, Marco +0000-0001-9292-9463 +Vital-IT group, SIB Swiss Institute of Bioinformatics, Quartier Sorge-BâtimentAmphipôle, CH- 1015 Lausanne Switzerland Marco. Pagni @ sib. swiss; https: // orcid. org / 0000 - 0001 - 9292 - 9463 +agni@sib.swiss + + + +Author + +Rabet, Nicolas +Sorbonne Universités, Muséum national d’Histoire naturelle, UCN, UA, CNRS, IRD, Biologie des organismes et écosystèmes aquatiques, BOREA, UMR 8067, CP 26 75231, 43 rue Cuvier, 75005, Paris Cedex 05, France. + +text + + +Zootaxa + + +2023 + +2023-04-13 + + +5264 + + +2 + + +205 +220 + + + + +http://dx.doi.org/10.11646/zootaxa.5264.2.3 + +journal article +53819 +10.11646/zootaxa.5264.2.3 +c8918fb6-3f25-4521-9f65-1e4effc251f0 +1175-5326 +7836432 +5991F65F-7425-4B75-A576-42A4E42F5B17 + + + + + + + +Leptestheria nobilis +( +Sars, 1900 +) + + + + + + + +( +Figs. 8 +, +9 +) + + + + + +Leptestheriella nobilis +( + +Padhye +et al. +2011 + +) + + + + + +Material studied. + +Four +females and +three males +from +University of Pune Pond +(UoP pond) (18˚33′17.62″ N & 73˚49′26.80″ E), +Pune +collected in + +June 2010 + +(collected by +SMP +) + +. + + + + +Redescription. Male. + + +Head. +Broadly rectangular; eyes moderately sized, ocular tubercle conspicuous, shape of ocellus varying but mostly triangular; rostrum dilated and spatulate; occipital condyle prolonged and projecting posteriorly; L/W ratio ~0.9–1.0 with a pointed apex; sharp stout spine present at the tip of rostrum, thrice as long as wide and arched ( +Fig.9A +) + + +First antenna. +Long & bulbous, twice the length of the base of second antenna; about 5–8 lobes, each lobe lined with several sensillae. + + +Second antenna. +Bi-ramous with varying number of antennomeres, each antennomere bearing spiniform projections (5–8) anteriorly; spines long, slender with an acute tip; plumose setae on opposite sides ( +Fig. 8B +) + + +Carapace. +Length. 6.7 ± +0.7 mm +; Height. 3.6 ± +0.40 mm +. Oblong, broadly rectangular, dorsal and anterior margin straight, umbone prominence varying between populations (prominent in ‘tableland’ specimens but not in UoP pond), number of growth lines highly varying, 10–20 easily visible, dark brown or pinkish in coloration when alive. + + +Trunk. +Consists of 23–25 segments, each with a pair of thoracopods and decreasing in size posteriorly. First two thoracopods modified into claspers ( +Fig. 8A +). + + +Thoracopods I & II +. Broad, anterior portion of movable finger (endopod) wide but tapering and strongly arching distally (hooklike), apex of which is lined with numerous scales in both the claspers; large palp (endite 5) two segmented, nearly equal in length in the first clasper, distal segment 1.2 times in length than proximal segment in the second clasper; small palp (endite 4 outgrowth) cylindrical, ~2.5 times as long as the width of its base; palm (endite 4) roughly rectangular and projecting obtusely, a medial triangular protrusion observed at base of palm in both claspers gripping area of palm lined with spines which increase in size posteriorly. Other thoracopods having similar structure with 5 endites, an endopodite with digitiform lobes on the exopodites, decreasing in size posteriorly, the last 5–8 very small ( +Fig. 8C +). Each of the 8–23 segments has a group of short, posteriorly directed setae with acute apices, the number first increases, and then gradually decreases, a maximum of 7–8 setae per segment is observed. + + +Telson. +Broadly rectangular in outline, dorsal margin arched; the postero-lateral edge ending with a big spine, nearly half the length of the cercopod, curved, without any serration; dorsal margin lined with 30–40 spines, unequal in size and bearing serrations; telson terminal setae originating before the telson spines ( +Fig. 9C +) + + + +FIGURE 8. + +Leptestheria nobilis + +. A. Habitus (male), B. Second antenna (male), C. Clasper I (male), D. Cercopod (male) (Scale bars 1mm for A, 0.5 mm for B, D, 0.25mm for C). + + + +Cercopods. +Long and stout, about 0.8–0.9 the length of telson, straight, gradually narrowing to an acute slightly upturned apex; tip reaching the postero-lateral projection of the telson; eighty percent of the dorsal margin lined with small similar sized serrated spinules about +30–45 in +number ( +Fig. 9C +). + + +Redescription. Female. +Similar to male morphology but with some variations. Rostrum triangular in shape, L/ W ratio of ~ 1.0 ( +Fig. 9B +). Ninth and 10th thoracopods modified with extended epipodites for carrying eggs. Telson dorsal margin more gently arched than male and lined with 30–40 spines on the dorsal margin ( +Fig.9B +), cercopod morphology as in male ( +Fig. 8D +) + + + +FIGURE 9. + +Leptestheria nobilis + +. A. Head (male), B. Telson (male), C. Head (female), D. Telson (female) (Scale bars 1mm for A–D). + + + +Carapace. +Length +6.2 mm +± +0.4 mm +; height +4 mm +± +0.3 mm +. + + +Egg. +Spherical and with no ornamentation ( +Figs.4C & D +in Padhye +et al +, 2016) + + + + +Remarks +. The morphology of + +Leptestheria nobilis + +is highly variable ( +Simhachalam & Timms, 2012 +), although some of the characters observed in these populations, such as the shape of the occipital condyle and the structure of the cercopod, coincide with previous and original descriptions ( +Daday, 1923 +; +Sars, 1900 +). + +Leptestheria dumonti +Subash Babu & Bijoy Nandan, 2010 + +and + +Leptestheria simhadrii +( +Simhachalam & Timms, 2012 +) + +are very similar to + +L. nobilis + +in terms of their morphology and thus their species validity needs to be checked using integrative approaches. The studied population could also represent a distinct cryptic species, though, this cannot be confirmed unless topotypic information is obtained. This species was found in assemblages (see +Padhye & Dahanukar, 2015 +for all combinations of assemblages) or occurred alone. + + + + \ No newline at end of file diff --git a/data/38/4A/AE/384AAE1CFF99CC255D8EF8BBFDA23472.xml b/data/38/4A/AE/384AAE1CFF99CC255D8EF8BBFDA23472.xml new file mode 100644 index 00000000000..0d703e0d351 --- /dev/null +++ b/data/38/4A/AE/384AAE1CFF99CC255D8EF8BBFDA23472.xml @@ -0,0 +1,311 @@ + + + +New leptestherid clam shrimps (Pancrustacea: Branchiopoda: Spinicaudata Leptestheriidae) from peninsular India + + + +Author + +Padhye, Sameer M. +Biologia Life Science LLP, Ahmednagar, India. + + + +Author + +Kulkarni, Mihir R. +Laboratory for Conservation of Endangered Species, CSIR-CCMB, Hyderabad, Telangana, India. + + + +Author + +Pagni, Marco +0000-0001-9292-9463 +Vital-IT group, SIB Swiss Institute of Bioinformatics, Quartier Sorge-BâtimentAmphipôle, CH- 1015 Lausanne Switzerland Marco. Pagni @ sib. swiss; https: // orcid. org / 0000 - 0001 - 9292 - 9463 +agni@sib.swiss + + + +Author + +Rabet, Nicolas +Sorbonne Universités, Muséum national d’Histoire naturelle, UCN, UA, CNRS, IRD, Biologie des organismes et écosystèmes aquatiques, BOREA, UMR 8067, CP 26 75231, 43 rue Cuvier, 75005, Paris Cedex 05, France. + +text + + +Zootaxa + + +2023 + +2023-04-13 + + +5264 + + +2 + + +205 +220 + + + + +http://dx.doi.org/10.11646/zootaxa.5264.2.3 + +journal article +53819 +10.11646/zootaxa.5264.2.3 +c8918fb6-3f25-4521-9f65-1e4effc251f0 +1175-5326 +7836432 +5991F65F-7425-4B75-A576-42A4E42F5B17 + + + + + + + +Leptestheria gomantaki + +sp. nov. + + + + + + +( +Figs. 5 +, +6B +, +7B +) + + + +Leptestheria +sp. + +M089 ( + +Schwentner +et al. +2020 + +) + + + + +Etymology. +The species is named after the Indian name for the Goa region, Gomantak. + + + + + + +Type +locality. + +A dried temporary pool in sand dunes in +Benaulim +, +India +: +Goa +( +15°15′36″N +, +73°55′13″E +; Date of collection of sediment + +Oct 2016 + +). The absence of typical aquatic vegetation suggests that water is only present for a short time + +. + + +Type material +. + + +Holotype +. + +One +female (without carapace) (in 4% formalin + glycerin) deposited at the +Western Regional Centre of Zoological Survey +of +India +( +ZSI +), Pune (Registration number: ZSI-WRC C.2074) + + + +Other material estudied. +One female. + + + + +Description. Male. +Males were not obtained in the rehydrated sediments. + + + +Description. Female ( +holotype +). + + + +Head. +Eyes large, noticeable ocular tubercle but ocular notch not very conspicuous, ocellus elongated with a crescent shape, projecting fornix, rostrum triangular, spine present at the tip of rostrum, spine ~5 times as long as wide and arched, occipital condyle projecting but not prolonged with a pointed apex directed perpendicularly to the dorsal margin, L/W ratio of ~0.6. ( +Fig. 5A +). + + + +FIGURE 5. + +Leptestheria gomantaki + + +sp. nov. + +A. Head (female), B. Dorsal armature (female), C. Telson showing cercopod (female) (Scale bars 1mm for A, 0.5 mm for B,C). + + + +First antenna. +Bulbous and prolonged, more than two times the length of base of second antenna, about 6–8 lobes present on dorsal margin, each lobe lined with several sensillae. + + +Second antenna. +Bi-ramous with 14 flagellomeres, each flagellomere bearing about 3–8 long posteriorly projecting spines with acute apices on posterior surface and plumose setae on the anterior face. + + +Carapace. +Length. +6.3 mm +; Width +3.3 mm +( +holotype +carapace damaged; not measured). Roughly rectangular, straight dorsal and ventral margins, umbone prominent located on the anterior 1/3 +rd +of the carapace, carapace with 15 + distinct carapace lines, brown in coloration. + + +Trunk. +Trunk consisting of 24 segments, each with a pair of thoracopods and decreasing in size posteriorly, the last 6 very small. + + +Thoracopods. +As per the genus without any fingerlike exopodite projections, thoracopods 9 and 10 with long epipodites for carrying eggs. + + +Segments 13–24 +, each bearing bunch of stout posteriorly directed setae with acute apices, number increasing anteriorly first and then slightly decreasing, maximum of 5–7 setae seen per segment ( +Figs. 5B +, +7B +). + + +Telson. +Broadly rectangular; dorsal margin gently arched, the lateral edge ending with a big spine, ~0.3 times the length of the cercopod; dorsal margin lined with about 30 irregularly sized spines but largest at the posterior end, largest spines ~2 times the length of smallest spines ( +Figs. 6B +, +7B +). + + + +FIGURE 6. + +Leptestheria chalukyae + + +sp. nov. + +A. Telson (female); + +Leptestheria gomantaki + + +sp. nov. + +B. Telson (female) (Scale bars 0.5 mm for A–B). + + + +Cercopods +. Long, about ~1.1 times the length of dorsal margin of telson, highly arched and tapering posteriorly; tip exceeding the posterior lateral projection of the telson; 2/3 +rd +of the anterior part of the dorsal margin gradually increasing posteriorly with largest spines densely packed, the last few (4–5) as long as the breadth of the thickest region of the telson spine ( +Figs. 5C +, +6B +). + + + + +Remarks. +The female specimen ( +holotype +) described here was used for obtaining sequences (few limbs), which were subsequently used to generate the phylogeny by + +Schwentner +et al. +2020 + +(coded M089; + +Fig. +2 + +in + +Schwentner +et al. +2020 + +). Males of this species could not be obtained in the sediment rehydration. This species was still recognized as a distinct species because the unique head/cercopod morphology of the female amongst all the other Indian species. The cercopod structure of + +L. gomantaki + +resembles the Chinese species + +Leptestheria kunmingensis +Shu, Rogers, Chen & Yang, 2015 + +female ( + +Shu +et al. +2015 + +). This species was seen to co-occur with + +Eulimnadia bondi +, +Padhye, Rabet, Kulkarni & Pagni, 2018 + +. + + + + \ No newline at end of file diff --git a/data/38/4A/AE/384AAE1CFF9FCC275D8EFC80FDC53597.xml b/data/38/4A/AE/384AAE1CFF9FCC275D8EFC80FDC53597.xml new file mode 100644 index 00000000000..561cf3d630f --- /dev/null +++ b/data/38/4A/AE/384AAE1CFF9FCC275D8EFC80FDC53597.xml @@ -0,0 +1,389 @@ + + + +New leptestherid clam shrimps (Pancrustacea: Branchiopoda: Spinicaudata Leptestheriidae) from peninsular India + + + +Author + +Padhye, Sameer M. +Biologia Life Science LLP, Ahmednagar, India. + + + +Author + +Kulkarni, Mihir R. +Laboratory for Conservation of Endangered Species, CSIR-CCMB, Hyderabad, Telangana, India. + + + +Author + +Pagni, Marco +0000-0001-9292-9463 +Vital-IT group, SIB Swiss Institute of Bioinformatics, Quartier Sorge-BâtimentAmphipôle, CH- 1015 Lausanne Switzerland Marco. Pagni @ sib. swiss; https: // orcid. org / 0000 - 0001 - 9292 - 9463 +agni@sib.swiss + + + +Author + +Rabet, Nicolas +Sorbonne Universités, Muséum national d’Histoire naturelle, UCN, UA, CNRS, IRD, Biologie des organismes et écosystèmes aquatiques, BOREA, UMR 8067, CP 26 75231, 43 rue Cuvier, 75005, Paris Cedex 05, France. + +text + + +Zootaxa + + +2023 + +2023-04-13 + + +5264 + + +2 + + +205 +220 + + + + +http://dx.doi.org/10.11646/zootaxa.5264.2.3 + +journal article +53819 +10.11646/zootaxa.5264.2.3 +c8918fb6-3f25-4521-9f65-1e4effc251f0 +1175-5326 +7836432 +5991F65F-7425-4B75-A576-42A4E42F5B17 + + + + + + + +Leptestheria chalukyae + +sp. nov. + + + + + + +( +Figs.3 +, +4 +, +6A +, +7A +) + + + +Leptestheria +sp. + +M128 ( + +Schwentner +et al. +2020 + +) + + + + +Etymology. +The species is named after the great medieval Indian dynasty called Chalukyas (Badami Chalukyas) who ruled large parts of Southern/Central +India +and whose capital was Badami where these specimens were collected from. + + + + + + +Type +locality. + +A rock pool dug in red sandstone near +Badami +fort ( +India +: +Karnataka +) ( +15°55′17″N +, +75°41′3″E +; +Date +of collection of sediment, + +Oct 2016 + +) + +. + + +Type material +. + + +Holotype + +. +One +male (4% formalin + glycerin) deposited at the +Western Regional Centre of Zoological Survey +of +India +( +ZSI +), Pune (Registration number: ZSI-WRC C.2073). + + + +Other material studied. +Two females. + + + + + +Description. Male ( +holotype +). + + + +Head. +Broadly rectangular. Eyes large, noticeable ocular tubercle. Ocellus elongated and irregularly shaped, located at middle of rostrum. Prominent fornix. Rostrum broad and spatulate, occipital condyle rounded, barely projecting, spine present at the tip of rostrum ( +Fig.3B +), spine nearly three times as long as wide and gently arching. + + +First antenna. +Antenna long, bulbous, more than two times the length of base of second antenna; about 10–14 lobes present on dorsal margin, each lobe lined with several sensillae. + + +Second antenna. +Bi-ramous, endopod and exopod with 14 flagellomeres ( +Fig.3C +), length nearly twice the head length, each flagellomere bearing about 3–8 long posteriorly projecting spines with acute apices and plumose setae on opposite sides, flagellomere size decreasing posteriorly. + + +Carapace. +Length +7.6 mm +; Height +3.4 mm +. Oblong, dorsal and ventral margin straight, umbone prominent located on the anterior 1/3 +rd +of the carapace. Carapace with 10 + distinct carapace lines, light brown in coloration ( +Fig.3A +), ventral margin lined with fine setae. + + +Trunk. +Consisting of 26 segments ( +Fig.3C +), each with a pair of thoracopods and decreasing in size posteriorly, the last eight being the smallest. + + +Thoracopods I & II +. Modified as claspers. Both claspers large. Movable finger (endopod) broad anteriorly but narrowing and hook like distally in both claspers. Large palp (endite 5) two segmented in both claspers, both segments nearly equal in length in first clasper; distal segment about 1.3 times in length than proximal segment in the second clasper. Small palp (endite 4 outgrowth) cylindrically shaped, 2.5x as long as broad, directed posteriorly in both claspers, palm (endite 4) rectangular, as long as broad in the first clasper, marginally longer than broad in the second clasper, triangular protrusion observed medially at base of palm in both claspers, gripping area of the palm with small tubercles (smallest as long as broad) anteriorly and increasing gradually in size posteriorly ( +Fig. 4A +). Other thoracopods having similar structure with 5 endites as the other members of the genus, decreasing in size posteriorly, the last eigth very small. + + +Segments 16–26, each bearing bunch of stout posteriorly directed setae with acute apices dorsally ( +Fig. 3D +), number increasing anteriorly first and then gradually decreasing, maximum of 6–7 setae are seen per segment. + + +Telson. +Broadly rectangular in shape. Dorsal margin distinctly arched, the lateral edge ending with a big spine, ~0.4 times the length of the cercopod. Dorsal margin with ~30 irregularly sized spines, longest spines twice as long as broad and 2.5 times as long as the smallest spines. Telson filaments between 1 +stand +3 +rd +marginal spines ( +Fig.4B +). + + + +FIGURE 3. + +Leptestheria chalukyae + + +sp. nov. + +A. Carapace (male), B. Head (male), C. Habitus (male), D. Dorsal armature (male), E. Head (female), F. Cercopod tip (female) (Scale bars 1mm for A,B,C,E, 0.5mm for D, 0.1 mm for F). + + + +Cercopod. +Long, about 0.8 times the length of dorsal margin of telson, tapering posteriorly; margin gently curved until 2/3 +rd +of the length, tips dorsally and gradually upturned, tip at the same level as the postero-lateral projection of the telson; 2/3 +rd +of the anterior part of the dorsal margin lined with about 30 similar sized spinules, equally spaced ( +Fig. 4B +). + + +Female. +Similar to male morphology but with some variations. + + +Carapace size. +Length 6.7 & +6.3 mm +; Height 3.4 & +3.2 mm +. + + +Rostrum +triangular, rostral spine long, ~4 times as long as broad at the base; occipital condyle similar to male ( +Figs. 3E +, +7A +); + + +Telson +. Dorsal edge less convex than male lined with about 20 irregularly sized spines ( +Fig.6A +). + + + +FIGURE 4. + +Leptestheria chalukyae + + +sp. nov. + +A. Clasper I (male), B. Telson (male) (Scale bars 0.25 mm for A, 0.5 mm for B). + + + +Cercopods +highly arched, spines on the dorsal margin gradually increasing posteriorly with last 6–7 spines being about 0.7–0.8 times that of the breadth of the thickest region of the telson spine ( +Fig. 3F +). + + + + +Remarks +. The female described here was used (few limbs) for obtaining sequence which were subsequently used to generate the phylogeny by + +Schwentner +et al. +2020 + +(coded M128; + +Fig +2 + +in + +Schwentner +et al. +2020 + +). This species differs from the rest of Indian species based on the occipital condyle shape/length and the very big cercopod marginal spines in males. The rounded occipital condyle of + +L. chalukyae + + +sp. nov +. + +resembles with + +Eoleptestheria +species + +( + +E. ticinensis +(Balsamo-Crivelli, 1859)) + +. It is also relatively similar to the Indian species + +L. sarsi + +described from Telangana (a southern state in +India +). The cercopod spine size and arrangement in the male differs in these species with + +L. sarsi + +having 6–8 very big spines (length of the biggest spine is nearly 0.7–0.8 times the thickest region of the cercopod) near the tip of the cercopod ( +Fig.3D +in +Padhye & Rabet, 2017 +) which is absent in + +L. chalukyae + + +sp. nov. + +. The female condyle is relatively elongated in + +L. sarsi + +female ( +Fig. 3B +in +Padhye & Rabet, 2017 +). Remarkably, both + +L. chalukyae + +and + +L. sarsi + +were reported from rock pools suggesting potential local diversification of these temporary-water specialist organisms in peninsular +India +. + +Eulimnadia chaperi +(Simon, 1886) + +was seen coexisting with + +L. chalukyae + + +sp. nov +. + + + + + \ No newline at end of file diff --git a/data/38/4A/CC/384ACC7AD3DD9A3FB7A2247C50EF7CDD.xml b/data/38/4A/CC/384ACC7AD3DD9A3FB7A2247C50EF7CDD.xml new file mode 100644 index 00000000000..57166ca4bfe --- /dev/null +++ b/data/38/4A/CC/384ACC7AD3DD9A3FB7A2247C50EF7CDD.xml @@ -0,0 +1,86 @@ + + + +A Revision of the Stylasteridae (Cnidaria, Hydrozoa, Filifera) from Alaska and Adjacent Waters + + + +Author + +Cairns, Stephen D. + + + +Author + +Lindner, Alberto + +text + + +ZooKeys + + +2011 + +158 + + +1 +88 + + + + +http://dx.doi.org/10.3897/zookeys.158.1910 + +journal article +http://dx.doi.org/10.3897/zookeys.158.1910 +1313-2970-158-1 + + + + +Genus +Stylaster Gray, 1831 + + + +Diagnosis. +Colonies branching in a flabellum or a bush shape (in only one case lamellate). Coenosteum usually reticulate-granular but may be linear-imbricate; coenosteum of many colors and hardness. Gastro- and dactylopores arranged in conventional cyclosystem arrangement, with only one gastrostyle per cyclosystem; pores of the peripheral type; supernumerary dactylopores often present. Cyclosystems arranged on branch edges and/or on corallum faces, or uniformly on all branch surfaces, but not unifacially. Gastropore tube single-chambered, but may be constricted by a ring palisade. Dactylostyles present. Ampullae usually superficial. + + +Discussion. + +The genus and its various grouping are discussed by +Cairns (1983b) +and a key to all stylasterid genera, including the groups of +Stylaster +, is provided by +Cairns (1992) +. Currently there are 80 recognized Recent species and 7 fossil species ( +Appeltans et al. 2011 +: WoRMS data base: www.marinespecies.org). It is by far the most species-rich and diverse genus of the stylasterids. + + + +Type species. + +Madrepora roseus +Pallas, 1766, by subsequent designation ( +Milne Edwards and Haime 1850 +: xxii), a member of Group B. + + + +Distribution. + +Oligocene to Recent: cosmopolitan from depths of 0-2010 m ( +Cairns 1992 +; +Appeltans et al. 2011 +). + + + + \ No newline at end of file diff --git a/data/38/4A/E9/384AE95AFFD9FFED6BC75902FBCEFCE1.xml b/data/38/4A/E9/384AE95AFFD9FFED6BC75902FBCEFCE1.xml new file mode 100644 index 00000000000..aa5d32e55c8 --- /dev/null +++ b/data/38/4A/E9/384AE95AFFD9FFED6BC75902FBCEFCE1.xml @@ -0,0 +1,385 @@ + + + +Traumatomutilla André miscellanea: Revision of the bellica, bifurca, diabolica, and vitelligera species groups, and a new group for the new species T. pilkingtoni Bartholomay and Williams (Hymenoptera: Mutillidae: Sphaeropthalminae: Dasymutillini) + + + +Author + +Bartholomay, Pedro R. + + + +Author + +Williams, Kevin A. + + + +Author + +Luz, David R. + + + +Author + +Cambra, Roberto A. + + + +Author + +Oliveira, Márcio Luiz de + +text + + +Insecta Mundi + + +2019 + +2019-06-28 + + +709 + + +709 + + +1 +37 + + + +journal article +23949 +10.5281/zenodo.3674793 +98c3ec1f-1711-4f1d-acb6-1702ad46ddfb +1942-1354 +3674793 +63A67DA8-A6A5-47E4-97F0-FFFE3D66A58A + + + + + + + +Traumatomutilla pilkingtoni +Bartholomay and Williams + +, +sp. nov. + + + + + + +( +Fig. 66–69 +) + + + + +Diagnosis. Female. +In addition to the structural characters referenced in the species groups diagnosis, + +T. pilkingtoni + +can be defined by its orange-red head, T2 with a pair of longitudinally sub-ovate orangered integumental spots, and fringes of T2–4 mostly clothed with black setae. + + + + +Description. Female. +Body length +5–8 mm +. +Head +. Posterior margin nearly straight. Head width nearly equal to pronotal width. Eye length in frontal view 1.3 × distance from its ventral margin to mandibular condyle. Front vertex and gena densely foveolate, more sparsely so on transition area between front and vertex. Mandible unidentate. Dorsal scrobal carina well defined, narrowly separated from antennal tubercles; lateral scrobal carina virtually absent. Antennal tubercle shallowly and irregularly rugose. F1 1.85 × pedicel length; F2 virtually as long as pedicel. Genal carina present, broadly separated from gular carina and hypostomal carina. Occipital carina slightly swollen dorsolaterally. +Mesosoma +. Mesosoma 1.1 × as long as wide. Pronotum slightly wider than mesothorax. Mesosomal dorsum densely areolatepunctate, slightly denser posterad. Humeral carina present, disconnected from low rounded epaulet, slightly produced apically, antero-lateral corners of pronotum slightly angulate in dorsal view. Pronotal spiracle virtually flat against lateral margin of pronotum. Sculpture of lateral face of pronotum and mesosomal pleurae obscured by dense setae, except dorsal fourth of metapleuron asetose and impunctate. Lateral face of propodeum virtually impunctate, smooth, shinning with scattered small shallow punctures. Ratios of width of humeral angles, pronotal spiracles, widest point of mesonotum, narrowest point of mesonotum and propodeum posterior to propodeal spiracles, 75:78:76:66:57. Lateral margin of mesosoma not emarginated anterior to propodeal spiracle, smoothly diverging anterad. Propodeal spiracle slightly projected from lateral margin of mesosoma; post-spiracular area absent. Scutellar scale present, welldeveloped, arcuate in posterior view, as wide as and separated from conspicuous anterolateral carinae; anterolateral carinae connected to each other. Scabrous intervals absent on scutellar area. Posterior face of propodeum longer than dorsal face. +Metasoma +. T1 sub-nodose 0.4 × as wide as T2. T2 slightly longer than wide, with maximum width posterior to midlength. Disc of T2 densely foveolate to densely punctate mediad; sculpture sparser and larger posterolaterally and over integumental spots. T3–6, except pygidium, dense foveolate-punctate to dense punctate. S1 with conspicuous blunt longitudinal carina, slightly higher anteriorly. S2 sparse foveolate, sculpture smaller anterad; subapical transverse slope present, less conspicuous medially; antero-medial crest-fold absent. S3–6 dense coarse foveolate. Pygidium sub-ovate, defined by lateral carinae throughout its extension, except basal margin; surface irregularly rugose; rugae longitudinally interrupted, wavy; interstice apparently impunctate, smooth. + + +Coloration and variations. +Head, mesosoma, T1 and appendages orange-brown, darker on legs and antennal flagellomeres partially. Metasoma except T1 brownish-black with a pair of large longitudinally sub-ovate orange integumental spots on T2, nearly confluent medially. Body setae predominantly silverywhite to silvery-golden, except for black to reddish-black setae on the following: medial spot on vertex, mesosomal dorsum medially, T2 medially (except over integumental spots), T3–4 nearly entirely, and small areas on T5 posterolaterally. No conspicuous color or setae variations were observed for any of the females examined. + + + + +Figures 66–69. + +Traumatomutilla pilkingtoni +Bartholomay and Williams + +, +sp. nov. +, ♀, holotype. +66) +Dorsal habitus, line 2mm. +67) +Lateral habitus, line 2mm. +68) +Head, frontal view. +69) +T6 (pygidium), posterior view. + + + + +Distribution. +Argentina +( +Tucuman +, Cordoba and +Santiago del Estero +provinces). + + + + +Material examined. + +( +35♀ +) + + +Type material. +Holotype +, + +, + + + +ARGENTINA + +, + +Cordova + +, Balnearia, +ii.1971 +, Fritz ( +AMNH +). + + +Paratypes +, + +ARGENTINA + +, Gran +Chaco +, +1♀ +( +MNHN +) + +; + + +Tucumán + +, + +11km +N Cadillal + +, +1♀ +, + +03.iii.1990 + +, +J.G. Rozen +& +A. Roig +( +AMNH +); + + +1♀ +, +25.iii.1990 +, J.G. Rozen & A. Roig + +; + + +Santiago del Estero + +, +1♀ +, +Muséum Paris, E. +R +. +Wagner +1935 ( +MNHN +) + +; + +Añatuya. +6♀ +, + +iii.1979 + +, +Fritz +( +AMNH +) + +; + +Barrancas +, +Bañados de Rio Dulce +, + +60km +O D’Icaño + +, +3♀ +, 1909, E. +R +. +Wagner +( +MNHN +) + +; + +Outskirts of Icaño +, +Mistol Paso +, +1♀ +, janvier juin [i–vi?] 1912, E. +R +. +Wagner +( +MNHN +) + +; + +1♀ +, 1918, E. +R +. +Wagner +( +MNHN +) + +; + +Banks +of the +Salado River +, +1♀ +, + +xii.1910 + +, E. +R +. +Wagner +( +MNHN +) + +; + +Chaco +, +Rio Salado +, +1♀ +, avril [iv?] ( +MNHN +) + +; + + +Cordoba + +, +Balnearia +, +16♀ +, + +ii.1971 + +, +Fritz +( +AMNH +) + +; + +1♀ +, + +ii.1971 + +, +Fritz +( +CSCA +) + +. + + + + +Etymology: +This remarkable species, is named in honor of the British philosopher, comedian, radio personality, presenter, author, and actor Karl Pilkington due to its rounded orange head. + + + + +Remarks. +The reddish/orange head integument, silvery white setae patterns of the mesosoma, and integumental markings of the metasoma of + +T. pilkingtoni + +are remarkably similar to other species from the same area, such as + +Cephalomutilla haematodes +( +Gerstaecker, 1874 +) + +. + + + + \ No newline at end of file diff --git a/data/38/4A/E9/384AE95AFFDAFFEB6BC75CF0FC8DFD48.xml b/data/38/4A/E9/384AE95AFFDAFFEB6BC75CF0FC8DFD48.xml new file mode 100644 index 00000000000..c4e1534efb9 --- /dev/null +++ b/data/38/4A/E9/384AE95AFFDAFFEB6BC75CF0FC8DFD48.xml @@ -0,0 +1,147 @@ + + + +Traumatomutilla André miscellanea: Revision of the bellica, bifurca, diabolica, and vitelligera species groups, and a new group for the new species T. pilkingtoni Bartholomay and Williams (Hymenoptera: Mutillidae: Sphaeropthalminae: Dasymutillini) + + + +Author + +Bartholomay, Pedro R. + + + +Author + +Williams, Kevin A. + + + +Author + +Luz, David R. + + + +Author + +Cambra, Roberto A. + + + +Author + +Oliveira, Márcio Luiz de + +text + + +Insecta Mundi + + +2019 + +2019-06-28 + + +709 + + +709 + + +1 +37 + + + +journal article +23949 +10.5281/zenodo.3674793 +98c3ec1f-1711-4f1d-acb6-1702ad46ddfb +1942-1354 +3674793 +63A67DA8-A6A5-47E4-97F0-FFFE3D66A58A + + + + + + +pilkingtoni species group + + + + + + +Diagnosis. +Females of this species group can be defined by a unique combination of characters: head unarmed posterolaterally; mesonotum simply divergent anterad, not constricted anterior to propodeal spiracle; scutellar scale and anterolateral carinae distinct; apex of middle and hind femora rounded; T2 with two integumental spots; gena feebly carinate; pygidium ovate. + + + + +Included taxon. + +Traumatomutilla pilkingtoni +Bartholomay and Williams + +, + +sp. nov. + + + + + +Distribution. + +Traumatomutilla pilkingtoni + +has been recorded solely from southwestern Dry Chacos areas of +Argentina +. + + + + +Remarks. +Species groups of +Traumatomutilla +with small-bodied species tend to have the head posteriorly armed with tubercles, while larger +Traumatomutilla +lack these tubercles and have mesosomal armature. Interestingly, the small bodied + +T. pilkingtoni + +resembles small bodied members of the trochanterata and inermis groups but lacks head tubercles and various other traits. It does not, however, possess the diagnostic traits of any larger bodied groups either. In its lack of diagnostic features, it is somewhat similar to + +T. diabolica + +, which lives in similar habitats in +Argentina +, but these two species differ in other important +Traumatomutilla +features: head shape, T1 shape, pygidium shape and sculpture, number of spots, tergal fringes, etc. As in + +T. diabolica + +, eventual discovery of the male will be necessary to understand its relations to other species groups. + + +In the key to species groups ( +Williams et al. 2017 +), + +T. pilkingtoni + +keys out to the trochanterata group in couplet 16. It can be recognized by its broad pygidium ( +Fig. 69 +), while the trochanterata group has a slender pygidium (e.g. figure +16 in +Williams et al. 2017 +). + + + + \ No newline at end of file diff --git a/data/38/4A/E9/384AE95AFFE1FFD76BC75FD2FB70FB2D.xml b/data/38/4A/E9/384AE95AFFE1FFD76BC75FD2FB70FB2D.xml new file mode 100644 index 00000000000..60c3a1ab9a5 --- /dev/null +++ b/data/38/4A/E9/384AE95AFFE1FFD76BC75FD2FB70FB2D.xml @@ -0,0 +1,464 @@ + + + +Traumatomutilla André miscellanea: Revision of the bellica, bifurca, diabolica, and vitelligera species groups, and a new group for the new species T. pilkingtoni Bartholomay and Williams (Hymenoptera: Mutillidae: Sphaeropthalminae: Dasymutillini) + + + +Author + +Bartholomay, Pedro R. + + + +Author + +Williams, Kevin A. + + + +Author + +Luz, David R. + + + +Author + +Cambra, Roberto A. + + + +Author + +Oliveira, Márcio Luiz de + +text + + +Insecta Mundi + + +2019 + +2019-06-28 + + +709 + + +709 + + +1 +37 + + + +journal article +23949 +10.5281/zenodo.3674793 +98c3ec1f-1711-4f1d-acb6-1702ad46ddfb +1942-1354 +3674793 +63A67DA8-A6A5-47E4-97F0-FFFE3D66A58A + + + + + + + +Traumatomutilla virginalis +( +Gerstaecker, 1874 +) + + + + + + + +( +Fig. 56–60 +) + + + + + + +Mutilla virginalis + +Gerstaecker 1874: 67 + + +. +Holotype +(by monotypy) female, +Brazil +, (ZMB), examined. + + + + + +Ephuta +( +Traumatomutilla +) +virginalis + +André 1902: 56 + + +(new combination). + + + + + +Traumatomutilla virginalis + +André 1904: 40 + + +(new combination). + + + + + +Diagnosis. Female. +In addition to the structural characters referenced in the species groups diagnosis, + +T. virginalis + +can be defined by its mostly black head and dorsum of mesosoma, except for medial silverywhite to silvery-golden setae spot medially on vertex and longitudinal silvery-white to silvery-golden setae stripe medially on mesosomal dorsum. + + + + +Description. Female. +Body length +8-12 mm +. +Head +. Posterior margin virtually straight. Occipital carina equally wide throughout. Head width 0.9 × pronotal width. Eye almost circular, its length in frontal view 1.65 × the distance from its ventral margin to mandibular condyle. Front, vertex, and gena densely and coarsely foveolate-punctate. Genal carina well-defined, short. Mandibles slender, evenly arcuate inwards apicad, with small subapical tooth, unarmed ventrally and dorsally. Dorsal scrobal carina well defined, broadly separated from antennal tubercles and virtually absent lateral scrobal carina. Antennal tubercle irregularly and vestigially rugose. Flagellomere 1 2.9 × pedicel length; flagellomere 2 2.0 × pedicel length. +Mesosoma +. Mesosomal length 0.8 × width. Pronotum virtually as wide as mesothorax. Anterior face of propodeum distinct from dorsal face, short, vestigially longitudinally striate ventrally and coarsely foveolate-punctate dorsally. Mesosomal dorsum densely, sharply and finely areolate-punctate throughout; intervals aligned appearing to form sinuous longitudinal carinae. Humeral carina present, well developed, slightly produced apically, disconnected from slightly pronounced epaulet; antero-lateral corners of pronotum angulate in dorsal view. Pronotal spiracle virtually flat against lateral margin of pronotum. Sculpture of lateral face of pronotum, mesosomal pleurae and lateral face of propodeum predominantly micropunctate, except for dorsal third and anterior margin of lateral face of pronotum sharply foveolate-punctate, mesopleural ridge densely foveolate-punctate; anterior and posterior margins of lateral face of propodeum sparsely foveolate-punctate. Post-spiracular area defined, virtually impunctate. Ratios of width of humeral angles, pronotal spiracles, widest point of mesonotum, narrowest point of mesonotum and propodeum posterior to propodeal spiracles, 80:86:84:68:63. Lateral margin of mesosoma not constricted, simply diverging anterad and converging slightly posterior to pronotal spiracles. Scutellar, anterolateral carinae and scabrous intervals of scutellar area absent. Propodeal spiracle virtually flat against lateral margin of mesosoma. Posterior face of propodeum as long as dorsal face. +Legs. +Meso and metafemora strongly truncate apicolaterally; truncation deeply sulcate; apex of metafemora strongly and sub-acutely projected posteriorly. +Metasoma +. Ratios of width of T1, width of T2 and length of T2, 34:75:68. T2 maximum width posterior to midlength. Disc of T2 densely and finely foveate-punctate; sculpture overall larger and sparser laterad and on integumental spots. T3–6, except pygidial plate, densely and finely foveate-punctate. S1 anteriorly with vestigial longitudinal blunt crest. S2 sparsely foveolate-punctate; antero-medial crest-fold and subapical slope absent; sculpture smaller and sparser posteromediad. S3–6 dense coarse foveolate-punctate. Pygidium broad, sub-ovate, defined by lateral carinae except at basal third; surface with well-defined, slightly sinuous, longitudinal, uninterrupted, subparallel costae; interstice granulose. + + + +Figures 51–55. + +Traumatomutilla bellica +( +Cresson, 1902 +) + +, ♀, holotype. +51) +Dorsal habitus, line 3mm. +52) +Lateral habitus, line 3mm. +53) +Head, frontal view. +54) +T6 (pygidium), posterior view. +55) +Holotype labels. + + + + +Figures 56–57 +. + +Traumatomutilla virginalis +( +Gerstaecker, 1874 +) + +, ♀, holotype, line 2mm. +56) +Dorsal habitus. +57) +Lateral habitus. + + + + +Figures 58–60. + +Traumatomutilla virginalis +( +Gerstaecker, 1874 +) + +, ♀, holotype. +58) +Head, frontal view. +59) +T6 (pygidium), posterior view. +60) +Holotype labels. + + + +Coloration and variations. +Body and appendages predominantly brownish-black to black, except mandibles and antennal flagellomeres partially orange-brown. Body setae predominantly brownish-black to black, with silvery-white to silvery-golden on the vertex, frons, gena, malar space, ventral surface of head; medial longitudinal stripe on propodeal dorsum; mesosomal pleurae; lateral felt line, lateral areas, lateral margins, and integumental spots of T2; T3–4 medially and laterally; T5 medially; and S1–4. Some specimens may have the medial longitudinal silvery-white setal stripe on the mesosomal dorsum restricted to the propodeum whilst others may have remnants of silvery-white setae reaching the anterior margin of pronotum. + + + + +Distribution. +Brazil +and +Paraguay +. + + + + +Material examined. + +( +18♀ +) + + +Type material. +Holotype +of + +Traumatomutilla virginalis + +, + +, BRAZIL, v. Olfers ( +ZMB +); + + + +Other material. +BRAZIL +: +Goiás +: + +2♀ +, 1912, +E. Gounelle +, ( +MNCN +, 163464, 163465) + +; + +2♀ +( +CUIC +) + +; + + +Minas Gerais +: + +1♀ +, +Reinhardt +( +ZMUC +) + +; + +10km +ao +S de São Gonçalo do Rio Preto +, +1♀ +, + +14.i.2005 + +, +Melo G.A. +R +. & +Costa +( +DZUP +) + +; + + +Mato Grosso do Sul +: + +Três Lagoas +, +1♀ +( +MZSUP +) + +; + +Três Lagoas +, marg. esq. +Rio Sucuriu +, +Faz Canaâ +, +1♀ +, + +10.xii.1967 + +, +Lane F. +( +MZSUP +) + +; + + +São Paulo +: + +Luis Antônio +, +Reserva de Jataí +, +1♀ +, + +16.x.1999 + +, +Melo G.A. +R +. ( +DZUP +) + +; + + +PARAGUAY +: +Concepción +: + +Cororo +, +1♀ +, + +25.ii.– 1.iii.1997 + +, +B. Garcete +( +MIUP +) + +; + +1♀ +, + +13–17.xi.1995 + +, C. +Aguilar +( +MIUP +) + +; + + +Amambay +, + +Parque Nacional Cerro Corá +, +1♀ +, + +17–18.v.2004 + +, +B. Garcete +( +MIUP +) + +; + + +San Pedro + +: +Rio Ypane +, +Cororo +, +5♀ +, + +ii.1979 + +, +M.A. Fritz +( +AMNH +) + +; + +1♀ +, + +xi.1983 + +, M.A. +Fritz +( +AMNH +) + +. + + + + +Remarks. +This species has only been recorded for the Chaco areas of +Paraguay +and Cerrado areas of +Brazil +. Additionally, its single longitudinal setal stripe on the mesosomal dorsum is uncommon in South American +Dasymutillini +, and is found only in some species of + +Suareztilla +Casal. + + + + + \ No newline at end of file diff --git a/data/38/4A/E9/384AE95AFFE2FFD06BC75AC9FDE8FCE0.xml b/data/38/4A/E9/384AE95AFFE2FFD06BC75AC9FDE8FCE0.xml new file mode 100644 index 00000000000..6b92124a989 --- /dev/null +++ b/data/38/4A/E9/384AE95AFFE2FFD06BC75AC9FDE8FCE0.xml @@ -0,0 +1,133 @@ + + + +Traumatomutilla André miscellanea: Revision of the bellica, bifurca, diabolica, and vitelligera species groups, and a new group for the new species T. pilkingtoni Bartholomay and Williams (Hymenoptera: Mutillidae: Sphaeropthalminae: Dasymutillini) + + + +Author + +Bartholomay, Pedro R. + + + +Author + +Williams, Kevin A. + + + +Author + +Luz, David R. + + + +Author + +Cambra, Roberto A. + + + +Author + +Oliveira, Márcio Luiz de + +text + + +Insecta Mundi + + +2019 + +2019-06-28 + + +709 + + +709 + + +1 +37 + + + +journal article +23949 +10.5281/zenodo.3674793 +98c3ec1f-1711-4f1d-acb6-1702ad46ddfb +1942-1354 +3674793 +63A67DA8-A6A5-47E4-97F0-FFFE3D66A58A + + + + + + +bellica species group + + + + + + +Diagnosis. +Females of this species group can be defined by a unique combination of characters: vertex unarmed, apex of middle and hind femora truncate, scutellar scale lacking, and T2 with only two integumental spots. Additionally, the genal carina is weak, the mesosoma is not elongate, and the pygidium is broadly ovate. + + + + +Included taxon. + +Traumatomutilla virginalis +( +Gerstaecker, 1874 +) + +and + +T. bellica +( +Cresson,1902 +) + +. + + + + +Distribution. +Species of the bellica group have been found so far in Chaco areas of +Paraguay +and Cerrado areas of +Brazil +. + + + + +Remarks. +The two species of this group can be differentiated most readily by coloration and distribution; + +T. bellica + +has the head and mesosomal dorsum setae entirely black ( +Fig. 51 +) and is known only from the Brazilian Cerrado, while + +T. virginalis + +has whitish setae on the propodeum and vertex dorsum ( +Fig. 56 +) and its distribution extends into the Paraguayan +Chaco +. + +Apart from the characters mentioned in the species group diagnosis, both species from the bellica group have two apparently exclusive characters: the metafemur is strongly and subacutely projected posterodistally, in contrast to having a truncate metafemur and the intervals of the dorsal mesosomal sculpture form longitudinal sinuous carinae. Some species of the inermis group appear to approximate the first character whilst some species of the trochanterata group appear to approximate the latter. In both of these groups, however, the posterior margin of the head is armed with tubercles, which are lacking in the bellica group. + + + \ No newline at end of file diff --git a/data/38/4A/E9/384AE95AFFE2FFD36BC759BAFBC3FA19.xml b/data/38/4A/E9/384AE95AFFE2FFD36BC759BAFBC3FA19.xml new file mode 100644 index 00000000000..a947777bb10 --- /dev/null +++ b/data/38/4A/E9/384AE95AFFE2FFD36BC759BAFBC3FA19.xml @@ -0,0 +1,345 @@ + + + +Traumatomutilla André miscellanea: Revision of the bellica, bifurca, diabolica, and vitelligera species groups, and a new group for the new species T. pilkingtoni Bartholomay and Williams (Hymenoptera: Mutillidae: Sphaeropthalminae: Dasymutillini) + + + +Author + +Bartholomay, Pedro R. + + + +Author + +Williams, Kevin A. + + + +Author + +Luz, David R. + + + +Author + +Cambra, Roberto A. + + + +Author + +Oliveira, Márcio Luiz de + +text + + +Insecta Mundi + + +2019 + +2019-06-28 + + +709 + + +709 + + +1 +37 + + + +journal article +23949 +10.5281/zenodo.3674793 +98c3ec1f-1711-4f1d-acb6-1702ad46ddfb +1942-1354 +3674793 +63A67DA8-A6A5-47E4-97F0-FFFE3D66A58A + + + + + + + +Traumatomutilla bellica +( +Cresson, 1902 +) + + + + + + + +( +Fig. 51–55 +) + + + + + + +Mutilla bellica + +Cresson 1902: 40 + + +. +Holotype +(designated by +Cresson +(1916: 80)) female, +Brazil +, [ +Mato Grosso do Sul +], Chapada [ +dos Guimarães +] (CMNH), examined. + + + + + +Ephuta +( +Traumatomutilla +) +bellica + +André 1902: 54 + + +(new combination). + + + + + +Traumatomutilla bellica + +André 1904: 40 + + +(new combination). + + + + + +Diagnosis. Female. +In addition to the structural characters referenced in the species groups diagnosis, + +T. bellica + +can be defined by its entirely black head and dorsum of mesosoma, and its longitudinal yellow integumental spots on T2. + + + + +Description. Female. +Body length +8-10 mm +. +Head +. Posterior margin nearly straight. Occipital carina uniformly wide throughout; tubercles of vertex absent. Head width 0.8 × pronotal width. Eye almost circular, its length in frontal virtually 1.4 × the distance from its ventral margin to mandibular condyle. Front, vertex, and gena densely and coarsely foveolate-punctate, more finely so on gena and malar space; intervals slightly scabrous on front. Genal carina present, well defined, short, broadly separated from gular carina. Mandibles with small subapical tooth, unarmed ventrally and dorsally. Dorsal scrobal carina present, narrowly separated from antennal tubercles and broadly separated from lateral scrobal carina; lateral scrobal carina reduced to longitudinal impunctate smooth area. Antennal tubercles sculpture indistinct, apparently irregularly smooth. Flagellomere 1 2.5 × pedicel length; flagellomere 2 1.75 × pedicel length. +Mesosoma +. Mesosoma 0.8 × as long as wide. Pronotum slightly wider than mesothorax. Anterior face of propodeum distinct from dorsal face, short, vestigially longitudinally striate ventrally and coarsely foveolate-punctate dorsally. Mesosomal dorsum densely, sharply and finely areolate-punctate throughout; intervals aligned appearing to form sinuous longitudinal carinae. Humeral carina present, well developed, slightly produced apically, disconnected from slightly pronounced epaulet; antero-lateral corners of pronotum angulate in dorsal view. Pronotal spiracle virtually flat against lateral margin of pronotum. Sculpture of lateral face of pronotum predominantly micropunctate, except dorsal third sharply areolate-punctate and anterior margin sparsely foveolate-punctate. Mesopleuron sculpture predominantly micropunctate, except along mesopleural ridge sparsely foveolate-punctate. Metapleuron predominantly micropunctate, except ventral fourth coarsely foveolate-punctate and dorsal third unsculptured, smooth. Lateral face of propodeum micropunctate, for few scattered punctures along posterior and anterior margin. Post-spiracular area defined, with few sparse punctures. Ratios of width of humeral angles, pronotal spiracles, widest point of mesonotum, narrowest point of mesonotum and propodeum posterior to propodeal spiracles, 79:79:77:65:57. Lateral margin of mesosoma not constricted, simply diverging anterad and converging slightly posterior to pronotal spiracles. Scutellar, anterolateral carinae and scabrous intervals of scutellar area absent. Propodeal spiracle virtually flat against lateral margin of mesosoma. Posterior face of propodeum as long as dorsal face. +Legs. +Meso and metafemora strongly truncate apicolaterally; truncation deeply sulcate; apex of metafemora strongly and sub-acutely projected posteriorly. +Metasoma +. Ratios of width of T1, width of T2 and length of T2, 41:91:91. T2 maximum width posterior to midlength. Disc of T2 dense and coarse foveolate-punctate to coarse punctate; foveolations sparser and larger laterad and over integumental spots. T3–6, except pygidium, densely and coarsely foveolate-punctate. S1 anteriorly with vestigial longitudinal blunt crest. S2 sparsely foveolate-punctate; antero-medial crest-fold and subapical slope absent; sculpture smaller and sparser posteromediad. S3–6 dense coarse foveolate-punctate. Pygidium broad, sub-ovate, defined by lateral carinae except at basal third; surface with well-defined, slightly sinuous, longitudinal, uninterrupted, subparallel costae; interstice granulose. + + +Coloration and variations. +No significant color or setae variations were observed. Body and appendages color predominantly reddish-brown to black, except for mandibles and antennal flagellomers partially orange-brown, and T2 with a pair of longitudinally elliptical yellow spots. Body setae predominantly brownish-black to black, except for silvery-white to silvery-golden setae varying in density on the following: lateral face of prontum; mesosomal pleurae; lateral face of propodeum; lateral felt lines, lateral margins and lateral spots on fringe of T2; lateral and medial spots on fringe of T3–4; medial spot on fringe of T5; T6 except pygidium; and S1–4. + + + + +Distribution. +Brazil +. + + + + +Material examined. +( +14♀ +) +Type material. + +Holotype +of + +Traumatomutilla bellica + +, + +, +BRAZIL +, [ + +Mato Grosso + +], +Chapada +[dos +Guimarães +], [ +H.H. Smith +] ( +CMNH +). + +Other material. + + +BRAZIL + +, +Mato Grosso +, +Chapada dos Guimarães +, +4♀ +, + +15.xi.2013 + +, +Melo, G.A.R. +, +Luz, D.R. +, +Williams, K.A. +( +DZUP +); + + +2♀ +, + +16.xi.2013 + +, +Melo, G.A.R. +, +Luz, D.R. +, +Williams, K.A. +( +DZUP +) + +; + +2♀ +, + +13.xi.2013 + +, +Melo, G.A.R. +, +Luz, D.R. +, +Williams, K.A. +( +DZUP +) + +; + +1♀ +, + +12.xi.2013 + +, +Melo, G.A.R. +, +Luz, D.R. +, +Williams, K.A. +( +DZUP +) + +; + +Mato Grosso +, +Chapada +[dos +Guimarães +], [ +H.H. Smith +]: +1♀ +, v, ( +CMNH +); + + +2# +, x, ( +CMNH +) + +; + +1♀ +, v, ( +MNHN +) + +. + + + + +Remarks. +Five of the examined specimens were collected by H. H. Smith in Chapada dos Guimarães and formed the +type +series in +Cresson’s (1902) +paper. Over 100 years after these specimens were collected, nine additional females were collected by KAW and DRL in the same area. This strange species has apparently never been documented from any other locality. The color pattern for + +T. bellica + +approximates several other species from Chapada dos Guimarães, such as + +T. rectilineata +André + +, + +T. andrei +(Cresson) + +, and + +T. ipanema +(Cresson) + +, appearing to be in an intermediate stage between circular spots on T2 (as + +T. virginalis + +) and longitudinal spots as in the previously mentioned species. + + + + \ No newline at end of file diff --git a/data/38/4A/E9/384AE95AFFE5FFD76BC75EE6FD4CF900.xml b/data/38/4A/E9/384AE95AFFE5FFD76BC75EE6FD4CF900.xml new file mode 100644 index 00000000000..21a2ee90a81 --- /dev/null +++ b/data/38/4A/E9/384AE95AFFE5FFD76BC75EE6FD4CF900.xml @@ -0,0 +1,115 @@ + + + +Traumatomutilla André miscellanea: Revision of the bellica, bifurca, diabolica, and vitelligera species groups, and a new group for the new species T. pilkingtoni Bartholomay and Williams (Hymenoptera: Mutillidae: Sphaeropthalminae: Dasymutillini) + + + +Author + +Bartholomay, Pedro R. + + + +Author + +Williams, Kevin A. + + + +Author + +Luz, David R. + + + +Author + +Cambra, Roberto A. + + + +Author + +Oliveira, Márcio Luiz de + +text + + +Insecta Mundi + + +2019 + +2019-06-28 + + +709 + + +709 + + +1 +37 + + + +journal article +23949 +10.5281/zenodo.3674793 +98c3ec1f-1711-4f1d-acb6-1702ad46ddfb +1942-1354 +3674793 +63A67DA8-A6A5-47E4-97F0-FFFE3D66A58A + + + + + + +diabolica species group + + + + + + +Diagnosis. +The females of this species group can be separated from the other groups lacking posterolateral head tubercles by their simplified mesosoma: the scutellar scale is narrow; anterior transverse carinae and the, longitudinal mesonotal carina are absent the lateral mesonotal margins are rounded; the genal carina is present; and the femoral apices rounded. + + + + +Included taxon. + +Traumatomutilla diabolica +( +Gerstaecker, 1874 +) + +. + + + + +Distribution. +Bolivia +and +Argentina +. + + + + +Remarks. +Williams et al. (2017) +stated that the overall morphology of + +T. diabolica + +made it impossible to place this species in one of the more diverse large-bodied species groups such as the indica, juvenilis, and quadrinotata species groups. Discovery of males of this and other groups are necessary to understanding relationships within the genus. + + + + \ No newline at end of file diff --git a/data/38/4A/E9/384AE95AFFE5FFE86BC75CDAFD12F93B.xml b/data/38/4A/E9/384AE95AFFE5FFE86BC75CDAFD12F93B.xml new file mode 100644 index 00000000000..d8f3f0f0d35 --- /dev/null +++ b/data/38/4A/E9/384AE95AFFE5FFE86BC75CDAFD12F93B.xml @@ -0,0 +1,446 @@ + + + +Traumatomutilla André miscellanea: Revision of the bellica, bifurca, diabolica, and vitelligera species groups, and a new group for the new species T. pilkingtoni Bartholomay and Williams (Hymenoptera: Mutillidae: Sphaeropthalminae: Dasymutillini) + + + +Author + +Bartholomay, Pedro R. + + + +Author + +Williams, Kevin A. + + + +Author + +Luz, David R. + + + +Author + +Cambra, Roberto A. + + + +Author + +Oliveira, Márcio Luiz de + +text + + +Insecta Mundi + + +2019 + +2019-06-28 + + +709 + + +709 + + +1 +37 + + + +journal article +23949 +10.5281/zenodo.3674793 +98c3ec1f-1711-4f1d-acb6-1702ad46ddfb +1942-1354 +3674793 +63A67DA8-A6A5-47E4-97F0-FFFE3D66A58A + + + + + + + +Traumatomutilla diabolica +( +Gerstaecker, 1874 +) + + + + + + + +( +Fig. 61–65 +) + + + + + + +Mutilla diabolica + +Gerstaecker 1874: 76 + + +. +Holotype +(by monotypy) female, +Argentina +, +Rosario +(MLUH), examined. + + + + + +Ephuta +( +Traumatomutilla +) +diabolica + +André 1902: 55 + + +(new combination). + + + + + +Ephuta +( +Traumatomutilla +) +chilena + +André 1906: 48 + + +. +Lectotype +(designated here) female, +Chile +[ +Argentina +], +Neuquen +(MLUH), examined. Synonymized by + +Mickel 1964: 169 + +. + + + + + +Diagnosis. Female. +Head unarmed, sculpture distinctly and coarsely foveolate-punctate; mesosoma without scutelar scale, longitudinal medial carina or mesonotal lateral projections; T2 with four large, reddish integumental spots. + + + + +Description. Female. +Body length +13-15 mm +. +Head +. Posterior margin slightly convex. Head width 0.9 × pronotal width. Eye length in frontal view slightly longer than distance from its ventral margin to mandibular condyle. Front, vertex and gena densely and coarsely areolate-punctate to foveolate-punctate. Mandible with small subapical tooth. Dorsal scrobal carina present, well-defined, not reaching antennal tubercles and vestigial lateral scrobal carina. Antennal tubercle finely and irregularly rugose. Flagellomere 1 2.5 × pedicel length; flagellomere 2 1.8 × pedicel length. Genal carina present, broadly separated from gular carina. Occipital carina slightly swollen apicolaterally; tubercles of vertex absent. +Mesosoma +. Mesosoma 0.8 × as long as wide. Mesosoma densely and finely areolate-punctate, areolations larger and sparser laterad. Anterior face of propodeum defined, striated longitudinally except coarsely punctate at dorsal margin. Humeral carina present, not pronounced apically, disconnected from well-defined and slightly produced epaulet, anterolateral corners of pronotum rounded in dorsal view. Pronotal spiracle virtually flat against lateral margin of pronotum. Sculpture of lateral face of pronotum and mesosomal pleurae obscured by dense setae, except dorsal fourth of metapleuron asetose and impunctate. Lateral face of propodeum virtually unsculptured, smooth, with few scattered punctures. Ratios of width of humeral angles, pronotal spiracles, widest point of mesonotum, narrowest point of mesonotum and propodeum posterior to propodeal spiracles, 83:96:97:72:65. Lateral margin of mesosoma emarginated anterior to propodeal spiracle, slightly projected anterad. Propodeal spiracle conspicuously projected from lateral margin of mesosoma; post-spiracular well-defined, apparently unsculptured. Scutellar scale well-defined, slightly wider and more conspicuous than anterolateral carinae; anterolateral carinae, reduced, narrowly connected to each other, disconnected from scutellar scale. Scabrous intervals absent. Posterior face of propodeum longer than dorsal face. +Metasoma +. Ratios of width of T1, width of T2 and length of T2, 25:59:67. T2 with maximum width posterior to midlength. T2 disc densely and coarsely foveolate-punctate; sculpture sparse and larger laterad. S1 with coarse uneven longitudinal carina, equally high throughout. S2 sparse coarse foveolate-punctate; subapical transverse slope present, interrupted medially; antero-medial longitudinal crest-fold vestigial. S3–6 dense coarse foveolate-punctate. Pygidium sub-ovate, defined by lateral carinae, except at basal third; surface confusedly, irregularly and finely costate; costae subparallel, mostly interrupted; interstice granulose. + + +Color variations. +Body and appendages black, except mandibles and antennal flagellomeres partially reddish-brown; T2 with four large orange to red integumental spots. Body setae predominantly black, except for silvery-white setae varying in density on the following: most of ventral surface of head; malar space; ventral half of gena; lateral face of pronotum; mesosomal pleurae; lateral face of propodeum; propodeal dorsum laterally; T1 laterally; integumental spots, lateral areas, lateral margin and lateral felt line of T2; fringe of T2–3 medially and laterally; T4–6, except pygidium, medially; S1–4. Certain specimens may have vestigial lateral silvery-white setae stripes on the propodeal dorsum, whilst others have such lines well defined. + + + + +Distribution. +Argentina +. + + + + +Material examined. +( +10♀ +) +Type material. + +Holotype +of + +Traumatomutilla chilena + +, + +, + +[ +ARGENTINA +] + +, + +Neuquén + +, +[18]95 +( +MNHN +) + +; +Other material. + + +ARGENTINA + +, + +Salta + +, +Sumalao +, +2♀ +, + +iii.1991 + +, +M.A. Fritz +( +AMNH +) + +; + + +Tucuman + +, near +Las Cejas +, +1♀ +, + +20.iv.1968 + +, +C.C. Porter +( +USNM +) + +; + + +8km +N + +Cadillal +, +1♀ +, + +25.iii.1990 + +, +J.G. Rozen +& +A. Roig +( +AMNH +) + +; + + +Mendoza + +, +Estancia Pedregal +, +1♀ +, + +29.iii.1903 + +( +ZMUC +) + +; + +Dep. De Calamuchita +, +El Sauce +, +1♀ +, + +iv.1938 + +, +Manuel J. Viana +( +AMNH +) + +; + + +Buenos Aires + +, +Saladillo +, +1♀ +, + +26.ii.1911 + +( +UMSP +, compared with type + +Traumatomutilla chilena +(André) + +det. +Mickel +1931; compared with type + +Mutilla diabolica +(Gerstaecker) + +det. +Mickel +1931); + + +Srra. Ventana +, m. 200, +Pcla. B.As. +, +1♀ +, + +14.iii.1972 + +, +Bordón +( +AMNH +) + +; + + +Neuquén + +, +Choele Choel +, +1♀ +, + +i.1990 + +, +U. Fritz +( +AMNH +) + +. + + + + +Remarks. +Mickel (1964) +synonymized + +Ephuta +( +Traumatomutilla +) +chilena + +with + +T. diabolica + +without, however, providing any information on the designation of +holotypes +or +lectotypes +for either species. The type of + +Ephuta +( +Traumatomutilla +) +chilena + +has a 1931 label by Mickel identifying it as + +T. diabolica + +and a “cotype” label likely from André himself. The only specimen of + +T. diabolica + +from MLUH has no type labels whatsoever, simply a handwritten label identifying it as + +Mutilla diabolica + +, the locality label, Rozario [sic], and a control label from MLUH. Since this specimen matches the type of + +Traumatomutilla diabolica + +, and the type locality of the original description, a +holotype +labeled has been added to it. + +Traumatomutilla diabolica + +has been recorded from dry +Chaco +areas of +Argentina +and +Bolivia +, as well as Argentinian Montes. One specimen is recorded from a humid Pampas area in +Buenos Aires province +. Perhaps the only remarkable feature of this species is that it lacks the distinguishing characters of the typical large bodied +Traumatomutilla +of southern South America. Its color pattern is typical of the grasslands and xeric areas of +Argentina +. Additionally, to our knowledge this is the southernmost distribution for a species of +Traumatomutilla +. + + + + \ No newline at end of file diff --git a/data/38/4A/E9/384AE95AFFEEFFD16BC75C86FAA6F8B7.xml b/data/38/4A/E9/384AE95AFFEEFFD16BC75C86FAA6F8B7.xml new file mode 100644 index 00000000000..b5952c356c2 --- /dev/null +++ b/data/38/4A/E9/384AE95AFFEEFFD16BC75C86FAA6F8B7.xml @@ -0,0 +1,306 @@ + + + +Traumatomutilla André miscellanea: Revision of the bellica, bifurca, diabolica, and vitelligera species groups, and a new group for the new species T. pilkingtoni Bartholomay and Williams (Hymenoptera: Mutillidae: Sphaeropthalminae: Dasymutillini) + + + +Author + +Bartholomay, Pedro R. + + + +Author + +Williams, Kevin A. + + + +Author + +Luz, David R. + + + +Author + +Cambra, Roberto A. + + + +Author + +Oliveira, Márcio Luiz de + +text + + +Insecta Mundi + + +2019 + +2019-06-28 + + +709 + + +709 + + +1 +37 + + + +journal article +23949 +10.5281/zenodo.3674793 +98c3ec1f-1711-4f1d-acb6-1702ad46ddfb +1942-1354 +3674793 +63A67DA8-A6A5-47E4-97F0-FFFE3D66A58A + + + + + + + +Traumatomutilla oxira +Casal, 1969 + + + + + + + +( +Fig. 46–50 +) + + + + + +Tramatomutilla + +oxira + +Casal 1969: 294 + + +. +Holotype +female, +Brazil +, +Paraíba +, +Soledade +, +Juazeirinho +(AMNH), examined. + + + + + +Diagnosis. Female. +This species is separated from other members of the bifurca species group by having a genal carina, lacking a scutellar scale and, by the overall setal pattern with the head having black setae medially on the frons and vertex, mesosoma with silvery-white lateral stripes throughout and metasoma with a pair of closely spaced submedial spots of silvery-white setae. Additionally, the fringes of T2–5 have silvery-white setae only laterally and T2 is virtually devoid of dense and short setae laterally. + + + + +Figures 38–45. + +Traumatomutilla bifurca + +, ♂. +38, 42) +Genitalia, dorsal view. +39, 43) +Genitalia, ventral view. +40, 44) +Genitalia, internal view (penial valve removed). +41, 45) +Penial valve, external view. + + + + +Figures 46–50. + +Traumatomutilla oxira +Casal, 1969 + +, ♀, holotype. +46) +Dorsal habitus, line 2mm. +47) +Lateral habitus, line 2mm. +48) +Head, frontal view. +49) +T6 (pygidium), posterior view. +50) +Holotype labels. + + + + +Description Female. +Body length 08 mm. +Head +. Posterior margin virtually straight. Head width 0.9 × pronotal width. Eye length in frontal view 0.9 × distance from its ventral margin to mandibular condyle. Head sculpture completely concealed by dense setae, except ventral surface, irregularly coarsely and shallowly punctate. Mandible with small subapical tooth. Dorsal scrobal carina present, well-defined, reaching antennal tubercles and vestigial lateral scrobal carina; lateral scrobal carina reduced to longitudinal, interrupted, impunctate area. Antennal tubercle coarsely and irregularly rugose. Flagellomere 1 1.8 × pedicel length; flagellomere 2 1.3 × pedicel length. Genal carina present, broadly separated from gular carina and hypostomal carina. Occipital carina equally wide throughout, tubercles of vertex absent. +Mesosoma +. Mesosoma 0.8 × as long as wide. Mesosoma densely and coarsely areolate-punctate, areolations denser and smaller mediad. Anterior face of propodeum well-defined, vestigially striated longitudinally; micropunctate at dorsal third. Humeral carina present, narrowly connected to poorly defined low epaulet, anterolateral corners of pronotum rounded in dorsal view. Pronotal spiracle slightly projected from lateral margin of pronotum. Sculpture of lateral face of pronotum and mesosomal pleurae obscured by dense setae, except dorsal fourth of metapleuron asetose and impunctate. Lateral face of propodeum coarsely and confusedly sculptured. Ratios of width of humeral angles, pronotal spiracles, widest point of mesonotum, narrowest point of mesonotum and propodeum posterior to propodeal spiracles, 53:62:59:51:44. Lateral margin of mesosoma not emarginated anterior to propodeal spiracle, smoothly and slightly diverging anterad, converging slightly posterior to pronotal spiracles. Propodeal spiracle virtually flat against lateral margin of mesosoma; post-spiracular absent. Scutellar scale and anterolateral carinae absent. Scabrous intervals absent. Posterior face of propodeum longer than dorsal face. +Metasoma +. Ratios of width of T1, width of T2 and length of T2, 36:78:72. T2 virtually as wide as long, with maximum width posterior to midlength. Dorsal sculpture of metasoma mostly concealed by dense setae except laterally of T2 sparsely foveolate-punctate. S1 with coarse blunt longitudinal carina, equally high throughout. S2 dense coarse foveolate-punctate; subapical transverse slope absent; antero-medial longitudinal crest-fold absent. S3–6 dense coarse foveolate-punctate. Pygidium sub-ovate, defined by lateral carinae, except at basal fifth; surface with longitudinal interrupted subparallel costae; interstice rugose. + + +Coloration and variations +. Body and appendages reddish-brown to black. Body setae predominantly silvery-white, except for reddish-black to black setae on the following: medially on vertex and front, medially on mesosomal dorsum, medially on dorsal face of T1, most of T2 disc, and medially on T3–5. No significant color or setae variations have been observed in the specimens examined. + + +Male. +Unknown. + + + + +Material examined. +( +10♀ +) +Type material. + +Holotype +of + +Traumatomutilla oxira + +, + +, + +BRAZIL +, +Paraíba +, + +Soledade +, +Juazeirinho +, + +VI.1956 + +, +A.G.A. Silva +( +AMNH +) + +. + +Paratypes +of + +Traumatomutilla oxira + +, +2♀ +, same label data as holotype ( +AMNH +) + +. +Other material. + +5♀ +same label data as type series ( +DZUP +) + +; + + +Pernambuco +, + +Petrolina +, +09°19’44.2’’S +40°33’30.1’’W +, +1♀ +, + +24–26.iii.2018 + +, +Martins H.O.J. +( +CSCA +) + +; + +1♀ +, + +14–16.v.2018 + +, +Martins H.O.J. +( +CSCA +) + +. + + + + +Distribution. +Brazil +. + + + + +Host. +Unknown. + + + + +Remarks. +Williams et al. (2017) +noted that + +T. oxira + +was structurally different from + +T. bifurca + +. The genal carina, though reduced, is distinct in this species and there is no trace of any scutellar scale or anterolateral carinae in the scutellar area except for a slight change in the sculpture intervals, which are wider in relation to the remainder of the mesosomal dorsum. Additionally, + +T. oxira + +is apparently a more slender species in comparison with + +T. bifurca + +. This species is known only from a single locality in northeastern +Brazil +, no putative males for this species have yet been found. For that reason, we refrain from transferring this species into another species group or erecting a new group for the species. + + + + \ No newline at end of file diff --git a/data/38/4A/E9/384AE95AFFF5FFDC6BC758AFFEADF9CC.xml b/data/38/4A/E9/384AE95AFFF5FFDC6BC758AFFEADF9CC.xml new file mode 100644 index 00000000000..2e3e73f521d --- /dev/null +++ b/data/38/4A/E9/384AE95AFFF5FFDC6BC758AFFEADF9CC.xml @@ -0,0 +1,2015 @@ + + + +Traumatomutilla André miscellanea: Revision of the bellica, bifurca, diabolica, and vitelligera species groups, and a new group for the new species T. pilkingtoni Bartholomay and Williams (Hymenoptera: Mutillidae: Sphaeropthalminae: Dasymutillini) + + + +Author + +Bartholomay, Pedro R. + + + +Author + +Williams, Kevin A. + + + +Author + +Luz, David R. + + + +Author + +Cambra, Roberto A. + + + +Author + +Oliveira, Márcio Luiz de + +text + + +Insecta Mundi + + +2019 + +2019-06-28 + + +709 + + +709 + + +1 +37 + + + +journal article +23949 +10.5281/zenodo.3674793 +98c3ec1f-1711-4f1d-acb6-1702ad46ddfb +1942-1354 +3674793 +63A67DA8-A6A5-47E4-97F0-FFFE3D66A58A + + + + + + + +Traumatomutilla bifurca +( +Klug, 1821 +) + + + + + + + +( +Fig. 26–45 +) + + + + + + +Mutilla bifurca + +Klug 1821: 313 + + +. +Lectotype +female (designated here), +Brazil +, +Pará +, +Cametá +(ZMB) + + + + + +Ephuta +( +Ephuta +) +bifurca + +André 1902: 58 + + +(new combination) + + + + + +Mutilla bifurca + +Bradley 1916: 192 + + +( +incertae sedis +) + + + + + +Traumatomutilla ira + + +Casal 1969: +297 + + + +Holotype female, +Brazil +, +Paraíba +, Soledade, Juazeirinho (AMNH), examined, +syn. nov. + + + + + +Traumatomutilla bifurca + +Nonveiller 1990: 75 + + +(new combination) + + + + + +Diagnosis. Female. +This species is separated from other members of the bifurca species group by lacking genal carina and overall setae pattern with the head completely clothed in silvery-white, dorsum of pronotum and mesonotum completely black and two sublateral oblique longitudinal patches of appressed silvery-white setae on T2. +Male. +Males can be diagnosed by their conspicuously striated and raised medial plate of pygidium, one pair of tooth-like projections below mid-ocellus, genital cuspis which is conspicuously slender and broadened, dorsoventrally flattened and subacute apically. Additionally, the cuspis is virtually devoid of setae with the exception of a single oblique row of short setae subapically on ventral surface. + + + + +Description. Female. +Body length 8.0–12.0 mm. +Head +. Posterior margin flat, occipital carina conspicuously swollen apicolaterally. Head width 0.75 × pronotal width. Eye almost circular; its length in frontal view 0.9 × the distance between its lower margin and mandibular condyle. Sculpture of frons and vertex concealed by dense setae; gena sparsely, coarsely and shallowly foveate-punctate; genal carina absent. Mandible unidentate apically, unarmed ventrally and dorsally. Antennal scrobe with dorsal horizontal carina conspicuously projected into a small lamella narrowly before antennal tubercle; lateral scrobal carina absent. Antennal tubercle irregularly and coarsely rugose. Flagellomere 1 2.2 × pedicel length; flagellomere 2 1.5 × pedicel length. +Mesosoma +. Mesosomal length 0.85 × width; pronotum as wide as mesothorax. Anterior face of propodeum well-defined, densely and finely punctate in dorsal half with longitudinal striae on ventral half. Mesosomal dorsal sculpture mostly concealed by dense setae, coarsely and densely areolate-punctate where observable. Humeral carina well developed, slightly projected apically, terminating just before low and rounded epaulet; anterolateral corners of pronotum angulate in dorsal view. Pronotal spiracles virtually flat against lateral margin of pronotum. Lateral face of pronotum sparsely and superficially punctate. Sculpture of mesopleuron and lateral face of propodeum concealed by dense setae, except at smooth impunctate dorsal fourth of metapleuron. Post spiracular area apparently undefined, concealed by dense setae. Ratios of width of humeral angles, pronotal spiracles, widest point of mesonotum, narrowest point of mesonotum and propodeum posterior to propodeal spiracles, 53:62:60:48:45. Lateral margin of mesothorax slightly constricted anterior to propodeal spiracle. Scutellar scale well-defined, very narrower than anterolateral carinae; anterolateral carinae unequal, disconnected from each other and scutellar scale; scabrous intervals on scutellar area apparently indistinct, concealed by dense setae if present. Posterior face of propodeum longer than dorsal face. +Metasoma +. Ratios of width of T1, width of T2 and length of T2, 45:97:104. T2 with maximum width posterior to midlength. Sculpture of T1–6, except pygidium, mostly concealed by dense setae, except laterally on T2 sparsely and coarsely foveate-punctate. S1 with longitudinal sharp carina, higher posteriorly; S2–5 densely and coarsely foveate-punctate, more finely and densely so in S3–5; anteromedial crest-fold vestigially present on S2; subapical slope on S2 vestigial, observable only laterally. Pygidium ovate, defined by carinae along its entire length, with well defined longitudinal wavy costae; interstice apparently smooth; apical margin with minute transverse striae. + + +Male. +(Hitherto undescribed) Body length 8.0–12.0 mm. +Head. +posterolateral angles rounded, vertex conspicuously swollen posteromedially; head width 0.9 × pronotal width. Eyes almost rounded, slightly longitudinally ovate; ocelli small; OOD 4.8 × DLO, IOD 1.5 × DLO. Occipital carina distinct, strongly convex. Front, vertex and gena sculpture concealed by setae; front with a pair of tooth-like projections below median ocellus. Gena ecarinate. Antennal scrobe broadly concave, with prominent transverse dorsal carina extending from internal margin of eye to antennal tubercle, 2/3 of antennal tubercle height in lateral view. Clypeus weakly convex, densely setose, setae concealing sculpture, apical margin straight. Scape bicarinate. Flagellomere 1 1.8 × pedicel length; flagellomere 2 1.3 × pedicel length. Mandible obliquely tridentate apically, inner tooth larger than middle tooth; lacking dorsal or ventral projections; maxilla and labium elongate; maxillary palp 6-segmented, third and fourth segments slightly flattened and apically expanded, other segments almost cylindrical. Labial palp 4-segmented, second and third segments slightly flattened and apically expanded, other segments almost cylindrical. +Mesosoma. +Epaulets evident, slightly prominent, rounded, distad from humeral carina by more than its own length. Anterior face of pronotum densely micropunctate laterally and with a distinct, impunctate, shining and slightly concave area medially; lateral face of pronotum finely and densely punctate; dorsal face of pronotum densely setose, sculpture concealed. Meso and metapleuron sculpture concealed by setae; mesopleuron with acute tubercle on dorsal half; Tegula convex, glabrous except with long appressed setae anterolaterally. Mesonotum and scutellum densely punctured; notaulus absent, parapsis indistinguishable; scutellum slightly convex; axilla produced posterolaterally as truncate tooth, contiguously punctate but smooth posteriorly. Metanotum sculpture concealed by dense appressed setae. Propodeum strongly convex, entirely densely reticulate, except lateral face near metapleuron smooth. +Metasoma +. T1 sub-petiolate, 0.5 × as wide as T2, sculpture concealed by dense silvery-white setae. S1 with weakly pronounced ridge-like carina. T2 0.75 × as long as wide, observable sculpture with dense coarse punctures, sculpture concealed by dense silvery-white setae elsewhere. S2 sparsely and coarsely punctate, more sparsely so medially; with posteromedial, longitudinal, acutely sub-ovate pit filled with dense silvery-white setae. T3–5 with sculpture concealed by dense silvery-white setae. T6 densely and coarsely punctate. S3–4 sculpture concealed by dense silvery-white setae. S5–7 densely and coarsely punctate, except apical third of S7 impunctate and asetose; apical margin of S7 with weakly acute medial projection. Pygidium with raised striated medial plate surrounded by lateral carinae. +Wings. +Forewing with elongate sclerotized pterostigma, stigma length 2x its height; marginal cell broadly truncate apically; three submarginal cells, 3r-m ending before M. Legs. Mid and hind tibiae each without strong spines dorsally, distinct apical secretory pore on inner surface near base of inner spur; spurs straight on margins, not serrate. +Genitalia +. Parapenial lobe weakly digit-like apically. Paramere free length 1.15 × the free length of cuspis and 3.5 × the free length of digitus; virtually straight in dorsal view and weakly and gradually upcurved in lateral view, virtually asetose. Cuspis free length 3 × the free length of digitus. slightly sinuose throughout and slightly expanded apically in dorsal view, virtually straight throughout and sharp apically in lateral view; with a single subapical row of short setae ventrally. Digitus with numerous short setae basally on dorsal surface. Penis valve with strongly concave on internal surface, closely bidentate apically, apical distance between teeth 0.05 × length of valve; with few short setae on apical margin and subapically on external surface. + + +Coloration and variations. Female. +Body and appendages black except mandibles partially reddishbrown. Tibial spurs pale-yellow. Head setae predominantly silvery-white with dorsal half of gena and posterior margin of vertex having black setae. Mesosomal setae predominantly silvery-white except dorsum of pronotum, mesonotum, and dorsum of propodeum medially, with black setae. Legs setae predominantly silvery-white except tarsi setae partially black to reddish-black. Metasomal setae predominantly white, except T1 medially, T2 medially and sublaterally, T3 medially, and T4–5 sublaterally with black setae varying in density. No significant color variations were found in the females examined. +Male. +Body and appendages black. Tibial spurs yellowish-white. Wings hyaline brown, apical third infuscated brown on forewing; veins brown, hindwing completely hyaline. Head setae silvery-white. Mesosomal setae predominantly silvery-white, except mesonotum, tegulae, and scutellum with black setae. Legs setae silvery-white; tibial spurs white. Metasomal setae predominantly silvery-white, except posterior half of T2, T5 medially, T6–7, and S7 with brownish-black to black setae varying in density. No significant color variations were observed for any of the males examined. + + + + +Material examined. + +1733 + +, +71♂ +. + + +Type material. +Lectotype +of + +Traumatomutilla bifurca + +, + +, + + + +BRAZIL +, +Bahia + +, Sieber & Gomes ( +ZMB +). +Holotype +of + +Traumatomutilla ira + +, + +, + + + +BRAZIL +, +Paraíba + +, Soledade, Juazeirinho, +vi.1956 +, A.G.A. Silva ( +AMNH +). + + + +Other material. +BRAZIL +: +Pará +: + +Algodoal, Praia da Princesa, +1♀ +, +22.viii.1981 +, Edmar L. Oliveira ( +MPEG +); +Cachimbo +, +1♀ +, + +19.viii.1978 + +, +M.J.G. Hopkins +& +H.C. Hopkins +( +MPEG +) + +; + +Conceição do Araguaia +, +1♀ +, + +vii.1959 + +, M. +Alvarenga +( +MPEG +) + +; + +Mangabeira +, +Mocajuba +, +3♀ +, + +vii.1953 + +, +O. Rego +( +AMNH +) + +; + + +Maranhão +: + +Barreirinha +, +Parque Nacional Lençóis Maranhenses +, 02°39’80’’S 42°49’88’’W, +1♀ +, + +07.v.2016 + +, +J.A. Rafael +& +F.L. Oliveira +( +INPA +) + +; + +Barra do Corda +, +1♀ +, + +07.ii.1955 + +, Expedição do +Departamento de Zoologia +( +MPEG +) + +; + +Imperatriz +, +1♀ +, + +13.vi.1978 + +, +M.F. Torres +( +MPEG +) + +; + +Mirador +, Parque Estadual do Mirador, + +Base +da Geraldina + +, +12♀ +, + +28.viii–03.ix.2008 + +, +F. Limeira-de-Oliveira +( +CZMA +) + +; + +Riachão +, +Fazenda Altos +, +9♀ +, + +18–22.viii.2009 + +, +F. Limeira-de-Oliveira +( +CZMA +) + +; + +Caxias +, +Reserva Ecológica do Inhamum +, +5♀ +, + +02–11.ix.2005 + +, +M.M.B.G.J. Júnior +( +CZMA +) + +; + +Mirador +, Parque Estadual do Mirador, + +Base +da Geraldina + +, +5♀ +, + +22–26.viii.2006 + +, +F. Limeira-de-Oliveira +( +CZMA +) + +; + +Mirador +, Parque Estadual do Mirador, + +Base +da Geraldina + +, +5♀ +, + +26.viii.2006 + +, +F. Limeira-de-Oliveira +( +CZMA +) + +; + +Mirador +, +Parque Estadual do Mirador +, +Base dos Cágados +, +06°46’37’’S +45°06’34’’W +, +3♀ +, + +26.xi–03.xii.2011 + +, +F. Limeira-de-Oliveira +( +CZMA +) + +; + +Caxias +, +Reserva Ecológica do Inhamum +, +2♀ +, + +17.ix.2005 + +, +F. Limeira-de-Oliveira +( +CZMA +) + +; + +Caxias +, +Ecológica do Inhamum +, +2♀ +, + +30.viii.2005 + +, +F. Limeira-de-Oliveira +( +CZMA +) + +; + +Mirador +, +Parque Estadual do Mirador +, +Base dos Cágados +, +06°46’37’’S +45°06’34’’W +, +1♀ +, + +06.viii.2011 + +, +F. Limeira-de-Oliveira +( +CZMA +) + +; + +Mirador +, +Parque Estadual do Mirador +, +Base dos Cágados +, +06°46’37’’S +45°06’34’’W +, +1♀ +, + +27.ix–02.x.2011 + +, +F. Limeira-de-Oliveira +( +CZMA +) + +; + +Mirador +, +Parque Estadual do Mirador +, +Base dos Cágados +, +06°46’37’’S +45°06’34’’W +, +1♀ +, + +01–05.vi.2011 + +, +F. Limeira-de-Oliveira +( +CZMA +) + +; + +Mirador +, Parque Estadual do Mirador, + +Base +da Geraldina + +, +1♀ +, + +22viii–03.ix.2008 + +, +F. Limeira-de-Oliveira +( +CZMA +) + +; + +Caxias +, +Reserva Ecológica do Inhamum +, +1♀ +, + +25.viii.2005 + +, +F. Limeira-de-Oliveira +( +CZMA +) + +; + +Mirador +, +Parque Estadual do Mirador +, +Base da Geraldina +, +1♀ +, + +21–25.vi.2008 + +, F. +Limeira-de-Oliveira +, +J.A. Rafael +e +P.A.M. Moraes +( +CZMA +) + +; + +Mirador +, +Parque Estadual do Mirador +, +Base da Geraldina +, +06°37’25’’S +45°52’08’’W +, +4♂ +, + +30.vii–06. viii.2011 + +, +F. Limeira-de-Oliveira +& +D.W.A. Marques +( +CZMA +) + +; + +Mirador +, Parque Estadual do Mirador, + +Base +da Geraldina + +, +1♂ +, + +21–26.viii.2006 + +, +F. Limeira-de-Oliveira +( +CZMA +) + +; + +Mirador +, +Parque Estadual do Mirador +, +Povoado Pindaíba +( +Mel +), +06°39’44’’S +45°01’37’’W +, +1♂ +, + +01–05.vi.2007 + +, +F. Limeira-de-Oliveira +, +M.M. Abreu +& +J.S. Pinto-Júnio +( +CZMA +) + +; + +Mirador +, +Parque Estadual do Mirador +, +Posto Avançado do Mel +, +06°43’48’’S +45°00’22’’W +, +1♀ +, + +18–25.iii.2012 + +, +F. Limeira-de-Oliveira +& +D.W.A. Marques +( +CZMA +) + +; + +Mirador +, +Parque Estadual do Mirador +, +Base +dos +Cágados +, +06°46’37’’S +45°06’34’’W +, +1♂ +, + +26.xi–03.xii.2011 + +, +F. Limeira-de-Oliveira +& +D.W.A. Marques +( +CZMA +) + +; + +São Luis +, +Vila +Maranhao +, +1♀ +, + +29.ix.1992 + +, +R +. Cambra ( +MIUP +) + +; + +São Luis +, +Vinhais +, +1♀ +, + +23.ix.1992 + +, +D. Quintero +( +MIUP +) + +; + + +Piauí +: + +Parque Nacional de Sete Cidades +, +2♀ +, + +08.ii.2013 + +, M.L. +Oliveira +( +INPA +) + +; + +1♀ +, + +10.ii.2013 + +, P.C. +Grossi +( +INPA +) + +; + +BR135 +, +35 +km south of +Bom Jesus +, +2♀ +, + +01.ii.2001 + +, J.P. +Pitts +( +EMUS +) + +; + +Parque Nacional de Sete Cidades +, +2♂ +, + +07–13.ii.2013 + +, A. +Somavilla +( +INPA +) + +; + +Teresina +, +2♀ +m, + +19.vii.1993 + +, +A. Casimiro +( +MIUP +) + +; + + +Ceará +, + +M. +Calmon +[Miguel Calmon], +1♂ +, + +18.4.1909 + +, +Ducke +( +MNHN +) + +; + + +Rio Grande do Norte +: + +Natal +, +Lagoa Nova +, +1♀ +, + +24.iv.2011 + +, S.M.N. +T +. +Melo +( +UFRN +) + +; + +Natal +, +Campus +CB +UFRN, +1♀ +, + +03.iii.2008 + +, I. +V +. +Almeida +( +UFRN +) + +; + +Natal +, Campus +CB +UFRN, +1♀ +, + +25.xi.2008 + +, M.A. +Silveira +( +UFRN +) + +; + +Natal +, +Parque +das +Dunas +, +1♀ +, + +22.v.2008 + +, +M.G.C. Bezerra +( +UFRN +) + +; + +Nísia Floresta +, +Praia de Barreta +, +1♀ +, + +04.ii.2011 + +, +R +. +M.B. Silva +( +UFRN +) + +; + +Nísia Floresta +, +Estrada +de acesso à +FLONA +, +1♀ +, + +15.x.2005 + +, I. +Moreno +( +UFRN +) + +; + +Baixa Verde +, +1♀ +, +Mann +( +USNM +) + +; + + +Goiás +, + +Parque Nacional Chapada +dos +Veadeiros +, +9♂ +, 2005 ( +UFES +) + +; + +nr. +Araguaina +, +1♀ + +10–12.ix.1963 + +( +BMNH +) + +; + + +Paraíba +, + +Juazeirinho +, +Soledade +, +4♀ +, + +ix.1956 + +, C. +R +. +Gonçalves +( +DGMC +) + +; + +Juazeirinho +, +Soledade +, +4♀ +, + +ix.1956 + +, +A.G.A. Silva +( +FSCA +) + +; + +Juazeirinho +, +Soledade +, +2♀ +, + +vi.1956 + +, C. +R +. +Gonçalves +( +EMUS +) + +; + +Souza +, +1♀ +, + +29.xi.1938 + +, +A. Silva +( +FSCA +) + +; + +1240 + +, + +vi.1956 + +, A.G.A. +Silva +( +DZUP +) +Santa Luzia +, +1♀ +, + +vi.1956 + +, +A.G.A. Silva +( +FSCA +) + +; + +Santa Luzia +, +1♀ +, + +vii.1956 + +, +A.G.A. Silva +( +EMUS +) + +; + + +Tocantins +: + +Itaguatins +, +Ilha São Domingos +, +1♀ +, + +20.vii.1989 + +, +F.F. Ramos +( +MPEG +) + +; + +Jalapão +, +1♀ +, + +30.x.2005 + +, +C.A. Nogueira +( +CEUFT +) + +; + +Lagoa +da Confusão, +Campo +dos +Ipês +, +1♀ +, + +24.ix.2005 + +, +C.A. Nogueira +( +CEUFT +) + +; + +Dianopolis +, +1♀ +, + +16.i.1962 + +, +J. Bechyne +( +MIUP +) + +; + + +Mato Grosso +: + +Utiariti +, +Rio Papagaios +, +1♀ +, + +27.x.1966 + +, +Lenko +& +Pereira +( +MZUSP +) + +; + +1♀ +, + +29.x.1966 + +, +Lenko +& +Pereira +( +MZUSP +) + +; + +1♀ +, + +x.1966 + +, +Lenko +& +Pereira +( +MZUSP +) + +; + +1♀ +, + +22–31.x.1966 + +, +Lenko +& +Pereira +( +MZUSP +) + +; + +1♀ +, + +01–12.xi.1966 + +, +Lenko +& +Pereira +( +MZUSP +) + +; + +Chapada +, +2♀ +, x. ( +CMNH +), +1♀ +, iv. ( +CMNH +), +1♀ +, v. ( +CMNH +) + +; + +1♀ +, vi. ( +CMNH +) + +; + +Alto Xingú +, P. +Leonardo +[Posto Indígena Leonardo Villas-Bôas, +12°11’50”S +53°22’46”W +], +7♀ +, 1963, +R +. +Arlé +( +MPEG +) + +; + +Cuiabá +, +Coxipó +, +2♀ +, + +10.x.1988 + +, +Ulisses +M. +Bezerra +( +UFMT +) + +; + +Cuiabá +, +Salgadeira +, +1♀ +, + +28.v.1990 + +, +Luzia +( +UFMT +) + +; + +Cuiabá +, +2♀ +, + +05.x.1988 + +, +Laura +M. +Rodrigues +( +UFMT +) + +; + +Chapada +dos +Guimarães +, +Água Fria +, +1♀ +, + +10.v.1984 + +, +Sebastião Marcolino +( +UFMT +) + +; + +Nova Mutum +, +1♀ +, + +21.viii.1991 + +, +Humberto Fonseca +( +UFMT +) + +; + +Paranatinga +, +Fazenda Agrochapada +, +Córrego Santiago +, +3♀ +, + +18.viii.1990 + +, +Wellington Péche +( +UFMT +) + +; + +Santa Teresinha +, near +Barra do Tapirapé +, +2♀ +, + +14.i.1963 + +, B. +Malkin +( +CASC +) + +; + +Santa Teresinha +, near +Barra do Tapirapé +, +2♀ +, + +26.viii.1957 + +, B. +Malkin +( +CASC +) + +; + +Capitão Vasconcelos +, +Rio Tuatuari +, +Xingú Basin +, +1♀ +, + +31.vii.1957 + +, +B. Malkin +( +CASC +) + +; + +Barra do Tapirapé +, +1♀ +, + +11.xii.1962 + +, B. +Malkin +( +CASC +) + +; + +Barra do Corda +, +2♀ +, + +11.vii.1955 + +, +Exp. Dep. Zool. +( +CASC +) + +; + + +Mato Grosso do Sul +, + +Chapada +[dos Guimarães], +1♀ +, + +i.1960 + +, +Canuto Amann. +( +MZUSP +) + +; + + +Bahia +: + +[Chapada Diamantina], +Vila do Ventura +, +Morro do Chapéu +, +1♀ +, + +26.i.2011 + +, +T +. +Mahlmann +( +INPA +) + +; + +Camaçari +, +Barra do Jacuípe +, +3♀ +, + +21.ii.2010 + +, +A. Köhler +( +CESC +) + +; + +4 km +northwest of +Lençóis +, +1♂ +, + +22.x.1999 + +, +Freddy +( +UEFS +) + +; + +Lençóis +, +1♂ +, + +29.iv.1999 + +, +Freddy +( +UEFS +) + +; + +Guarajuba +, +Camacari +, +4♀ +, + +4.i.1992 + +, J. +Delabie +( +MIUP +), +2♀ +, + +24.vi.1993 + +( +MIUP +) + +; + +Sambaiba +, +1♀ +, + +20.x.1994 + +, +Nascimento +( +MIUP +) + +; + + +Minas Gerais +: + +Rosário Oeste +, +1♀ +, + +xi.1970 + +, +Dirings +( +MZUSP +) + +; + +1♀ +, + +xi.1971 + +, +Dirings +( +MZUSP +) + +; + +2♀ +, +Dirings +( +MZUSP +). +An +additional +50♂ +and +352♀ +from various localities in +Brazil +and different collections were also examined + +. + + + + +Distribution. +Brazil +. + + + + +Host. +Unknown. + + + + +Remarks. +The +lectotype +of + +Mutilla bifurca + +is herein officially designated because, although the specimen was labelled as a +lectotype +by Mickel ( +Fig. 31 +), the taxonomic act was never published. The taxonomic history of + +T. bifurca + +is uncertain regarding at what moment it was moved to +Traumatomutilla +. +André (1902) +moved the species from + +Mutilla +Linnaeus + +to + +Ephuta +Say + +s.l. +which contained most species that would eventually be included in + +Dasymutilla +Ashmead. +Bradley (1916) + +revised + +Ephuta + +s.s. +and provided a list of species north of +Mexico +whilst +Mickel (1928) +published the first comprehensive treatment of + +Dasymutilla + +. Unfortunately, neither author provided information on the status of the remaining species that once comprised + +Ephuta + +s.l. +Casal (1969) +was actually the first author to mention the combination + +Traumatomutilla bifurca + +without, however, providing any remarks about the species or stating that it was a new combination. Several specimens in different collections have identification labels from Mickel as + +Traumatomutilla bifurca + +(pers. com.) which is why we hypothesize that Casal assumed the species had already been moved into +Traumatomutilla +by Mickel even without any official publishing of the taxonomic act. +Casal (1969) +originally separated + +T. ira + +from + +T. bifurca + +by subtle, subjective and not easily observable characteristics, namely the sculpture of T2 above the lateral felt line and relative size of the setal patterns of T2, the limits of which are subjected to the interpretation of the observer. Neither difference was evident or even observable in any of the specimens analyzed, including reference material identified by Casal himself after 1969. Sparser setae laterally on T2 is common in several species of every species group of +Traumatomutilla +(e.g. + +T. latevittata +( +Cresson, 1902 +) + +, + +T. angustata +André, 1906 + +). Regarding the setal patterns of T2, we observed that specimens from more southern regions ( +Mato Grosso do Sul +and +Tocantins +cerrado areas) have the oblique stripes much shorter and wider, ending before the midline of T +2 in +some cases. This contrasts with specimens from north and northeastern cerrado or Caatinga areas which have long and slender setal stripes on T2. The +lectotype +falls between these two forms, with the setal stripes on T2 evidently longer than southern specimens and wider than northeastern specimens. Most specimens identified by Casal as + +T. ira + +are from Caatinga regions in northeastern +Brazil +, whilst specimens from Cerrado were usually identified as + +T. bifurca + +. We observed no structural or color characters to support separation between Caatinga and Cerrado specimens into distinct species. We have seen more than +120 specimens +from Cerrado, Caatinga and Amazon areas that cannot be differentiated based on the characteristics proposed by +Casal (1969) +. Consequently, we propose + +T. ira +Casal, 1969 + +as a junior synonym of + +T. bifurca + +. The males herein associated with + +T. bifurca + +were repeatedly and consistently collected in large numbers and in multiple areas where females of + +T. bifurca + +were commonly collected. Although + +T. bifurca + +overlaps in distribution with + +T. oxira + +in +Paraíba state +, these males can’t be considered as candidates for association with + +T. oxira + +because this species is apparently restricted to the locality of Juazeirinho and males and females of + +T. bifurca + +have been collected together in multiple other localities. + + + +Figures 26–27. + +Traumatomutilla bifurca +( +Klug, 1821 +) + +, ♀, lectotype, line 2mm. +26) +Dorsal habitus. +27) +Lateral habitus. + + + + +Figures 28–31. + +Traumatomutilla bifurca + +, ♀, lectotype. +28) +Head, frontal view. +29) +T6 (pygidium), posterior view. +30) +T2, lateral view. +31) +Lectotype labels. + + + + +Figures 32–33. + +Traumatomutilla bifurca + +, ♂, line 2mm. +32) +Dorsal habitus. +33) +Lateral habitus. + + + + +Figures 34–37. + +Traumatomutilla bifurca + +, ♂. +34) +Head, frontal view. +35) +Head, dorsolateral view (frontal tubercles in detail). +36) +T6 (pygidium), posterior view. +37) +T6 (pygidium), posterolateral view. + + + +In addition to the peculiar color characteristics of the bifurca species group, the ecarinate gena on the females, frontal tubercles and raised pygidium on the males set this group apart from most +Traumatomutilla +. Although male characteristics of + +T. bifurca + +are apparently unique and exclusive within the +Dasymutillini +, a large number of + +Dasymutilla + +females also have ecarinate gena and many species of + +Dasymutilla + +do not have integumental markings on T2, something that only occurs in the bifurca group within +Traumatomutilla +. This, however, does not indicate that + +T. bifurca + +could be transferred to + +Dasymutilla + +in the near future. This conclusion is supported by the fact that the phylogeny of +Williams (2012) +found evidence that +Traumatomutilla +and + +Dasymutilla + +are reciprocally monophyletic and that species of the latter are predominantly North or Central American ( +Williams and Pitts 2013 +; +Cambra et al. 2018 +). + + + + \ No newline at end of file diff --git a/data/38/4A/E9/384AE95AFFF7FFC76BC75D0FFDCEFD14.xml b/data/38/4A/E9/384AE95AFFF7FFC76BC75D0FFDCEFD14.xml new file mode 100644 index 00000000000..554d7550e88 --- /dev/null +++ b/data/38/4A/E9/384AE95AFFF7FFC76BC75D0FFDCEFD14.xml @@ -0,0 +1,136 @@ + + + +Traumatomutilla André miscellanea: Revision of the bellica, bifurca, diabolica, and vitelligera species groups, and a new group for the new species T. pilkingtoni Bartholomay and Williams (Hymenoptera: Mutillidae: Sphaeropthalminae: Dasymutillini) + + + +Author + +Bartholomay, Pedro R. + + + +Author + +Williams, Kevin A. + + + +Author + +Luz, David R. + + + +Author + +Cambra, Roberto A. + + + +Author + +Oliveira, Márcio Luiz de + +text + + +Insecta Mundi + + +2019 + +2019-06-28 + + +709 + + +709 + + +1 +37 + + + +journal article +23949 +10.5281/zenodo.3674793 +98c3ec1f-1711-4f1d-acb6-1702ad46ddfb +1942-1354 +3674793 +63A67DA8-A6A5-47E4-97F0-FFFE3D66A58A + + + + + + +bifurca species group + + + + + + +Diagnosis. +Females can be diagnosed by lacking integumental markings on T2, the presence of contrasting patterns of black and white setae, head unarmed posterolaterally, genal carina absent or weakly defined, mesosoma compact, scutellar scale and anterior transverse carina present, mid and hind femora rounded apically, and pygidium broadly ovate. Males can be diagnosed by having the pygidium with a raised medial plate surrounded by lateral carinae and the head having a pair of blunt tooth-like projections on the front. + + + + +Figures 18–25. + +Traumatomutilla fascinata + +, ♂, holotype. +18, 22) +Genitalia, ♂, dorsal view. +19, 23) +Genitalia, ♂, ventral view. +20, 24) +Genitalia, ♂, internal view (penial valve removed). +21, 25) +Penial valve, ♂, external view. + + + + +Included taxa. + +T. bifurca +( +Klug, 1821 +) + +and + +T. oxira +Casal, 1969 + +. + + + + +Distribution. +Brazil +. + + + + +Remarks. +Species of the bifurca species group are marked by a contrasting pattern of black and white setae, making them some of the most easily recognizable within the genus. Additionally, they are among the few species of +Traumatomutilla +that show almost no variation in color or setae patterns. Although the two included species are separated by multiple structural features, as noted in their diagnoses below, they are most readily and easily differentiated by color pattern, particularly in the mesosomal stripes and T2 markings ( +Fig. 26 +, +46 +). + + + + \ No newline at end of file diff --git a/data/38/4A/E9/384AE95AFFFFFFC56BC75EF1FA63F974.xml b/data/38/4A/E9/384AE95AFFFFFFC56BC75EF1FA63F974.xml new file mode 100644 index 00000000000..40cfca20d16 --- /dev/null +++ b/data/38/4A/E9/384AE95AFFFFFFC56BC75EF1FA63F974.xml @@ -0,0 +1,1386 @@ + + + +Traumatomutilla André miscellanea: Revision of the bellica, bifurca, diabolica, and vitelligera species groups, and a new group for the new species T. pilkingtoni Bartholomay and Williams (Hymenoptera: Mutillidae: Sphaeropthalminae: Dasymutillini) + + + +Author + +Bartholomay, Pedro R. + + + +Author + +Williams, Kevin A. + + + +Author + +Luz, David R. + + + +Author + +Cambra, Roberto A. + + + +Author + +Oliveira, Márcio Luiz de + +text + + +Insecta Mundi + + +2019 + +2019-06-28 + + +709 + + +709 + + +1 +37 + + + +journal article +23949 +10.5281/zenodo.3674793 +98c3ec1f-1711-4f1d-acb6-1702ad46ddfb +1942-1354 +3674793 +63A67DA8-A6A5-47E4-97F0-FFFE3D66A58A + + + + + + + +Traumatomutilla vitelligera +( +Gerstaecker, 1874 +) + + + + + + + +( +Fig. 1–25 +) + + + + + + +Mutilla vitelligera + + +Gerstaecker 1874: 71 + + + +. +Holotype +(by monotypy) female, +Peru +(ZMB), examined. + + + + + +Mutilla diligens + +Smith 1879: 214 + + +. +Holotype +female, +Venezuela +(BMNH). Synonymized by + +Mickel 1964: 171 + +. + + + + + +Mutilla fascinata + + +Smith 1879: 217 + + + +. +Holotype +(by monotypy) male, +Peru +(BMNH), examined, +syn. nov. + + + + + +Ephuta +( +Traumatomutilla +) +vitelligera + +André 1902: 57 + + +, taxonomic position. + + + + + +Mutilla fascinata + +André 1902: 73 + + +, + +incertae sedis + +. + + + + + +Ephuta +( +Traumatomutilla +) +comata + + +André 1906: 67 + + + +. +Lectotype +(designated here) male, +Ecuador +, +Guayaquil +(MNHN), examined, +syn. nov. + + + + + +Sphaeropthalma salaverensis + +Rohwer 1913: 449 + + +( +holotype +female, coast of +Peru +, Desert of Salaverry, +15 vi 1911 +(USNM 15115), examined. Synonymized by + +Mickel 1964: 171 + +. + + + + + +Traumatomutilla fascinata +: + +Mickel 1964: 169 + + +, +new combination + + + + + +Traumatomutilla vitelligera +: + +Mickel 1964: 171 + + +, +new combination +. + + + + + +Diagnosis. Female. +In addition to structural characters referenced in the species groups diagnosis, + +T. vitelligera + +can be diagnosed by the following: head mostly clothed with silvery-white setae, mesosomal setae almost entirely black. Sculptured area on mesopleural ridge broad, densely and coarsely areolatepunctate. +Male. +Males of + +T. vitelligera + +can be diagnosed by their unique color pattern: having entirely black integument with head mostly and T3–5 completely clothed with dense silvery-white setae as well as blunt tubercles on dorsal half of mesopleuron, truncate axillar projections, and elongate hypopygium. + + + + +Description. Female. +Body length +15–18 mm +. +Head +. Posterior margin straight, occipital carina slightly swollen apicolaterally. Head width 0.75 × pronotal width. Eye almost circular; its length in frontal view 0.9 × distance between its lower margin and mandibular condyle. Frons and gena densely and coarsely areolate-punctate; vertex sculpture concealed by dense setae. Genal carina present, short, uneven, poorly defined. Mandible with small subapical tooth, unarmed dorsally and ventrally. Antennal scrobe dorsal carina present, well-defined, narrowly separated from antennal tubercles and reduced lateral scrobal. Antennal tubercle vestigially rugose. Flagellomere 1 2.7 × pedicel length; flagellomere 2 1.6 × pedicel length. +Mesosoma +. Mesosomal length 0.85 × width; pronotum as wide as mesothorax. Mesosomal dorsum densely and finely areolate-punctate. Anterior face of pronotum well-defined, vestigially longitudinally striate basally and sparse coarse punctate apically. Humeral carina well developed, terminating well before epaulet; projected apically; anterolateral corners of pronotum angulate in dorsal view. Pronotal spiracle virtually flat against lateral margin of pronotum. Lateral face of pronotum finely, shallowly foveate-punctate with interspersed micropunctures and inconspicuous impunctate swelling anteroventral to pronotal spiracle. Mesopleuron micropunctate throughout, except along mesopleural ridge dense coarse areolate punctate. Metapleuron sculpture mostly concealed by dense setae, except basal fourth coarsely and densely reticulate and apical fourth impunctate. Lateral face of propodeum sparsely, coarsely and shallowly foveate-punctate, more densely, coarsely and deeply so posterad. Ratios of width of humeral angles, pronotal spiracles, widest point of mesonotum, narrowest point of mesonotum and propodeum posterior to propodeal spiracles, 50:58:57:45:40. Lateral margin of mesothorax slightly constricted anterior to propodeal spiracle. Scutellar scale well-defined; anterolateral carinae connected to each other forming a single transverse carina narrowly reaching propodeal spiracles laterally and wider than scutellar scale; anterolateral carinae and narrowly connected to scutellar scale sublaterally; scabrous intervals absent. Propodeal spiracles moderately projected from lateral margin of mesosoma. Propodeum convex in lateral view, posterior face longer than dorsal face; post-spiracular area undefined. +Legs +. Mid and hind femora truncate apico-externally, truncation slightly sulcate. +Metasoma +. Ratios of width of T1, width of T2 and length of T2, 33:69:68. T2 with maximum width posterior to mid length. Disc of T2 densely and coarsely foveolate-punctate throughout, more densely, coarsely and confusedly so mediad; sculpture shallower and sparser on integumental spots. T3–5 densely foveolate-punctate with interspersed fine punctures. S1 with pronounced longitudinal carina equally high throughout. S2 coarsely and densely foveolate-punctate, more sparsely and finely so postero-mediad; S3–5 densely foveolate-punctate; anteromedial crest-fold present on S2; subapical slope on S2 reduced, nearly absent medially. Pygidium broad, sub-ovate, defined by lateral carinae, except at basal third; with fine dense irregular rugosities; interstice coarsely granulose. + + +Male. +Body length 11.0–16.0 mm. +Head +. Lateral margins not parallel behind eyes, posterolateral angles rounded. Head width 0.7 × pronotal width. Eye almost circular. Ocelli small; OOD 3.8 × DLO, IOD virtually equal to DLO. Vertex and gena densely, finely and partially confusedly foveate-punctate; frons sculpture concealed by dense setae. Gena ecarinate. Dorsal carina of antennal scrobe prominent, transverse, starting at eye margin and ending before antennal tubercle. Clypeus weakly convex medially, concave laterally immediately below antennal insertion; finely and densely punctate; with a pair of small tooth-like projections medially on apical margin. Scape bicarinate, inner carina less prominent. Flagellomere 1 1.7 × pedicel length; flagellomere 2 2 × pedicel length. Mandible obliquely tridentate apically, inner tooth slightly larger than middle tooth; lacking dorsal or ventral projections. +Mesosoma +. Epaulets inconspicuous, poorly defined, reduced to a narrow micropunctate area starting at anterior face of pronotum and ending on small rounded area on anterior margin of dorsal face of pronotum, disconnected from humeral carina. Sculpture of anterior face of pronotum finely and densely punctate, less densely so medially and micropunctate anterior to epaulets; lateral and dorsal faces coarsely and confusedly areolate-punctate to foveolate-punctate. Tegula convex, mostly glabrous and impunctate, except densely punctate anterior third. Mesoscutum densely, coarsely and confusedly areolate-punctate to foveolate-punctate, notaulus and parapsis absent. Scutellum convex, densely, coarsely and confusedly areolate-punctate. Axilla produced posterolaterally as truncate projection, coarsely, densely and confusedly foveolate-punctate, except impunctate posterior margin. Metanotum narrower medially, with lateral oblique micropunctate areas immediately posterior to hindwing insertion; sculpture densely and coarsely reticulate medially. Propodeum convex, densely and coarsely areolate; sculpture less defined along anterior margin of lateral face; dorsal face of propodeum slightly depressed sublaterally and with longitudinal irregular carina medially; posterolateral corners of dorsal face slightly pronounced, slightly angulate; dorsal and posterior face subequal in length. Mesopleuron densely and coarsely areolatepunctate to foveolate-punctate, with conspicuous blunt medial projection on dorsal half. Metapleuron virtually smooth, with sparse inconspicuous micropunctures, except ventral fourth, immediately above hind coxa, dense and coarse areolate-punctate. +Wings +. Forewing with moderate elongate sclerotized pterostigma; marginal cell elongated, truncate apically; three submarginal cells, apical veins of third cell weak. +Metasoma +. T1 0.4 × as wide as T2. T2 length 0.9 × its width. T1–2 densely, finely and confusedly foveolate-punctate, more sparsely so anterad on T1; sculpture of T3–6 concealed by dense setae, T7 with pygidial area irregularly rugose and weakly defined by carinae apicolaterally. S1densely, coarsely and confusedly areolate-punctate to foveolate-punctate; with longitudinal uneven and medially pronounced carina. S2 sparsely and irregularly foveolate-punctate with interspersed micropunctures along lateral margins, weakly swollen longitudinally at base, with small posteromedian pit densely filled with setae. S3–6 densely and coarsely foveolate-punctate to punctate, less densely so on S7. S7 trapezoidal, longer than broad, with a pair of closely spaced tooth-like projections on apical margin. +Genitalia +. Parapenial lobe inconspicuously pronounced apically. Ratios of free length of paramere, cuspis and digitus, 73:62:20. Paramere conspicuously sinuous throughout in dorsal view, slightly upcurved apically in lateral view; ventrally with dense medial tuft of long setae in addition to scattered, inconspicuous, short and thin setae throughout. Cuspis slightly sinuous in dorsal view and virtually straight in lateral view; slightly expanded apically in dorsal and lateral views; with small apical tuft of setae. Digitus short, weakly curved inward in dorsal view and upcurved in lateral view; with short setae dorsally, setae more numerous at base. Penis valve strongly concave on internal surface, with two sharp apical teeth on ventral margin apical distance between teeth 0.1 × length of valve; few strong short setae along apical margin and subapically on external surface. + + +Coloration and variations. Female. +Integumental coloration is predominantly black with mandibles and antennal flagellomeres partially reddish-brown; T2 with four yellow to orange integumental spots. Head setae predominantly black with the vertex clothed with silvery-white setae. Mesosomal setae predominantly black, except most of mesopleuron, most of metapleuron, lateral face of propodeum, ventral half of posterior face of propodeum with silvery-white setae varying in density. Legs setae silvery-white, tibial spurs yellowish-white. Metasomal setae predominantly black except for part of T1, lateral felt line and lateral setae of T2, fringe of T2–4, most of T5–6 and most of S1–6 with silverywhite setae varying in density. Some females differ by having more extensive silvery-white setae on the head or on the size of the integumental spots of T2 which can be conspicuously larger and much more closely spaced. The extent of white setae areas on the metasoma may also vary, especially on S2–4 on which it may be greatly reduced to the point of lacking on the fringes of S +2–3 in +some cases. +Male. +Body integument color entirely black, Forewing always dark fuscous with basal third and small medial spots brownish-hyaline, veins brown; hindwing overall lighter than forewing with basal third hyaline. Head setae predominantly silvery-white, with gena, malar space and posterior margin of vertex having black setae. Mesosomal setae predominantly black with silvery-white setae varying in density medially on metanotum, posterior and lateral face of propodeum, and basal third of mesosomal pleurae. Legs setae predominantly black except few silvery-white setae on femora and dense silvery-white setae on internal surface of hind tibia. Metasomal setae predominantly black except with most of T1, T2 basolaterally, felt lines, fringe of T3–5 and S3–5, posteromedian pit of S2 and disc of S2 partially, with silvery-white setae varying in density. + + + + +Material examined. +57♀ +, +19♂ +Type material. + +Holotype +of + +Traumatomutilla vitelligera + +, + +, +PERU +, ( +ZMB +) + +. + +Holotype +of + +Traumatomutilla fascinata + +, + +, +PERU +, ( +BMNH +) + +. + +Holotype +of + +Traumatomutilla salaverensis +, + + +, +Peru + +. + +Lectotype +of + +Traumatomutilla comata + +, + +, +ECUADOR +, +Guayaquil +, +1901 +, +Buchwald +( +MNHN +) + +. + +Paralectotype +of + +Traumatomutilla comata + +, + +, same label data as lectotype ( +MNHN +) + +. +Other material. + + +CHILE +: +Tacna +, + +Tacna +, +1♀ +, +D.S. Bullock +( +USNM +). + + + +ECUADOR +: +Esmeraldas + +, +San Mateo +, +1♀ +, 143202, ( +MNCN +) + +; + +South America +, +1♀ +, +ii–vii.1911 +, +S.N. Roads +( +ANSP +) + +; + +1♀ +, ( +ZMUC +) + +; + + +Manabi + +, +Portoviejo +, +1♂ +, + +22.xii.1971 + +, +M. Cooper +( +BMNH +) + +; + +Jama +, + +100 m +. + +, +2♀ +, + +13.vi.2001 + +, +D. Curoe +( +MIUP +) + +; + + +[ +Guayas +] + +, +Guayaquil +, +1♂ +, +Buchwald +( +MNHN +) + +; + + +El Oro + +, + +2 miles +north of + +Santa Rosa +, +1♂ +, + +24.i.1955 + +( +AMNH +) + +; + +Guayas +, +Daule +, +1♀ +, + +x.1981 + +, +G. Onore +( +MIUP +). + +PERU +: + +3♀ +, ( +EMUS +) + +; + +1♂ +, +1919 +, +J. De Gaulle +( +USNM +) + +; + +2♂ +, ( +EMUS +) + +; + +Toznamela +[sic!], +1♀ +( +USNM +) + +; + + +Piura +: + +Amotopa Mts. +[ +Cerros de Amotape +], +1♀ +, + +28.ix.1941 + +, +H.E.F. +( +AMNH +) + +; + +Sullana +, +2♀ +, + +02.ix.1944 + +, +P.A. Berry +( +USNM +) + +; + +2♀ +, + +15.viii.1943 + +, +P.A. Berry +( +USNM +) + +; + + +Lambayeque +: + +Lambayeque +, +1♀ +, + +03.iii.1981 + +, +M.E. Irwin +( +INHS +) + +; + +Pampa northwest of +Oyotun +[ +Pampa de Chumbenique +], +1♀ +, + +15.i.1985 + +, +J.M. Carpenter +( +USNM +) + +; + +Chiklaya +[ +Chiclayo +], +2♂ +, + +06.ii.1931 + +, +H.A. Jaynes +( +USNM +) + +; + + +10 km +south of + +Olmos +, +1♂ +, + +27.iii.2005 + +, +M.E. Irwin +( +EMUS +) + +; + + +10km +S Olmos + +, km52 +Olmos +road marker, +malaise in deciduous dry forest +, +06°01.55’S +79°40.82’W +, + +265m + +, +1♀ +, + +27–31.iii.2005 + +, +M.E. Irwin +& +F.D. Parker +( +EMUS +) + +; + + +Amazonas + +, [ +Utcubamba +], + +8 km +west of + +Bagua Grande +, +1♂ +, + +08.iii.2005 + +, +M.E. Irwin +( +EMUS +) + +; + + +8km +W Bagua Grande + +, +05°43’.02’S +78°31.68’W +, km216 on +Bagua +rd, +malaise across damp wash +, + +530m + +, +1♀ +, + +08–31.iii.2005 + +, +M.E. Irwin +& +F.D. Parker +( +EMUS +) + +; + + +Cajamarca +: + +[ +San Miguel +], +Nanchoc Quebrada +, +1♀ +, + +1–17.i.1985 + +, +J.M. Carpenter +( +USNM +) + +; + + +6 km +north of + +Chamaya +, +1# +, + +14.xi.2007 + +, +Irwin +& +Parker +( +EMUS +) + +; + + +6km +N Chamaya + +, + +2km + +W +Mochenta +on rd to +Valillo +, + +850m + +, +05°47.95’S +78°47’84’W +, +1♂ +, + +14–17.xi.2007 + +, +M.E. Irwin +& +F.D. Parker +( +EMUS +) + +; + + +San Martin +: + + +23 km +south of + +Picota +, +1♂ +, + +09.xi.2007 + +, +M.E. Irwin +( +EMUS +) + +; + +[ +La Libertad +], +Trujillo +, +1♀ +, + +17.xi.1936 + +, +H.A. Jaynes +( +DGMC +) + +; + +[ +Ancash +], +Casma +, +San Rafael +, +2♀ +, + +01.iv.1912 + +, +C.J. Townsend +( +USNM +) + +; + + +Pasco +, + +Pozizo +[ +Pozuzo +], +1♀ +, +P. Vaquero +( +CMNH +) + +; + + +Lima +: + +Cartavio +, +9♀ +, + +17.iii.1935 + +, +E.G. Smyth +( +EMUS +) + +; + +1♀ +, + +21.iii.1935 + +, +E.G. Smyth +( +EMUS +) + +; + +1♀ +, + +15.iii.1937 + +, +E.G. Smyth +( +EMUS +) + +; + +1♀ +, + +15.i.1937 + +, +E.G. Smyth +( +EMUS +) + +; + +1♀ +, + +08.iii.1937 + +, +E.G. Smyth +( +EMUS +) + +; + +3♂ +, + +03.iii.1935 + +, +E.G. Smyth +( +EMUS +) + +; + +4♀ +, + +03.iii.1935 + +, +E.G. Smyth +( +EMUS +) + +; + +1♀ +, + +03.iv.1935 + +, +E.G. Smyth +( +EMUS +) + +; + +3♀ +, + +13.iii.1935 + +, +E.G. Smyth +( +EMUS +) + +; + +1♀ +, + +03.iii.1937 + +, +E.G. Smyth +( +EMUS +) + +; + +Lima +, +1♀ +, + +01.i.1939 + +, +Weyrauch +( +CMNH +) + +; + +1♀ +, + +02.ii.1939 + +, +C.J. Drake +( +USNM +) + +; + +Verrugas +, +1♀ +, + +07.iv.1928 + +, +R.C. Shannon +( +USNM +) + +; + +Chosica +[railstation east of +Lima +], +1♂ +, +P. Vaquero +( +UMSP +) + +; + +North Central coast +, +1♀ +, + +01.iv.1951 + +( +AMNH +) + +;; + +San Miguel +, +1♀ +, + +08.iii.1955 + +, +W. Markl +( +MNCN +) + +; + + +Ica +: + +Huacachina +, +2♀ +, +E. Escomal +( +AMNH +) + +. + + + + +Figures 1–2. + +Traumatomutilla vitelligera +( +Gerstaecker, 1874 +) + +, holotype, line 2mm. +1) +Dorsal habitus. +2) +Lateral habitus. + + + + +Figures 3–6. + +Traumatomutilla vitelligera +( +Gerstaecker, 1874 +) + +, ♀. +3) +Head, frontal view, holotype. +4) +Head, frontal view, Lambayeque, Peru. +5) +T6 (pygidium), posterior view, holotype. +6) +Holotype labels. + + + + +Figures 7–8. + +Traumatomutilla comata +André, 1906 + +, ♂, lectotype, line 2mm. +7) +Dorsal habitus. +8) +Lateral habitus. + + + + +Figures 9–13. + +Traumatomutilla comata + +, lectotype; +9) +Head, frontal view. +10) +T6 (pygidium), posterior view. +11) +Mesosoma, dorsal view. +12) +Metasoma, dorsal view. +13) +Lectotype labels. + + + + +Figures 14–15. + +Traumatomutilla fascinata +( +Smith, 1879 +) + +, ♂, holotype, line 5mm. +14) +Dorsal habitus. +15) +Lateral habitus. + + + + +Figures 16–17. + +Traumatomutilla fascinata + +, ♂, holotype. +16) +Head, frontal view. +17) +Holotype labels, + +T. fascinata + +. + + + + +Distribution. +Ecuador +, +Peru +, +Chile +. + + + + +Host. +Unknown. + + + + +Remarks. +The distinctive setae pattern in + +T. vitelligera + +can be approximated by other species that have their bright mesosomal setae patches lost or obscured due to specimen wear or condition. According to +Nonveiller (1990) +, this species has been recorded from +Peru +, +Venezuela +, +Ecuador +, +Brazil +, +Paraguay +and +Chile +. However, we have only seen valid records of + +T. vitelligera + +from +Ecuador +, +Peru +and +Chile +and hypothesize the historical records from other countries are based on misidentified or mislabeled specimens. Examination of the types of + +T. fascinata + +and + +T. comata + +, as well as dissection of the genitalia of both species, indicate that they are virtually identical, except that the silvery-white setae areas on + +T. comata + +are less extensive and conspicuous than on + +T. fascinata + +. Additionally, both the +lectotype +and +paralectotype +of + +T. comata + +have an incomplete vein arising from the +rs +vein at the first submarginal cell ending halfway towards the base of the pterostigma. Given that the remaining characteristics of these specimens are virtually identical to specimens of + +T. fascinata + +, this abnormal vein is possibly some sort of malformation or teratoma, or a case of intraspecific variation. Additionally, variations in the venation of the right and left forewing of a mutillid may occur in the same specimen ( +Quintero and Cambra 2005 +). With the exception of a few species from the inermis and indica species groups in northwestern +Colombia +, + +T. vitelligera + +, + +T. fascinata + +and + +T. comata + +are the only species of +Traumatomutilla +to occur west of the Andes. Therefore, we associate + +T. vitelligera + +with + +T. fascinata + + +syn. nov. + +and + +T. comata + + +syn. nov. + +based on their overlapping geographical distribution and congruence of taxonomically important characters. + + + + \ No newline at end of file diff --git a/data/38/4A/E9/384AE95AFFFFFFCD6BC75BC0FE9DFB39.xml b/data/38/4A/E9/384AE95AFFFFFFCD6BC75BC0FE9DFB39.xml new file mode 100644 index 00000000000..d0573ddeeec --- /dev/null +++ b/data/38/4A/E9/384AE95AFFFFFFCD6BC75BC0FE9DFB39.xml @@ -0,0 +1,148 @@ + + + +Traumatomutilla André miscellanea: Revision of the bellica, bifurca, diabolica, and vitelligera species groups, and a new group for the new species T. pilkingtoni Bartholomay and Williams (Hymenoptera: Mutillidae: Sphaeropthalminae: Dasymutillini) + + + +Author + +Bartholomay, Pedro R. + + + +Author + +Williams, Kevin A. + + + +Author + +Luz, David R. + + + +Author + +Cambra, Roberto A. + + + +Author + +Oliveira, Márcio Luiz de + +text + + +Insecta Mundi + + +2019 + +2019-06-28 + + +709 + + +709 + + +1 +37 + + + +journal article +23949 +10.5281/zenodo.3674793 +98c3ec1f-1711-4f1d-acb6-1702ad46ddfb +1942-1354 +3674793 +63A67DA8-A6A5-47E4-97F0-FFFE3D66A58A + + + + + + +vitelligera species group + + + + + + +Diagnosis. +Females of this species group are identified by a unique combination of characters: head unarmed posterolaterally; mesonotum rounded laterally, lacking longitudinal medial carina; scutellar scale distinct, connected to anterior transverse carina; apex of middle and hind femora truncate; T2 having four integumental spots; gena carinate; pygidium broadly ovate. Males can be diagnosed by having the parameres conspicuously sinuous, with an isolated medial tuft of long setae ventrally; cuspis virtually straight and overall asetose, except for a small tuft of short setae apically. External characters include white meso- and metatibial spurs, truncate axilla, mesopleuron with blunt tubercle; hypopygium trapezoidal and T3–5 entirely clothed with white setae. + + + + +Included taxon. + +Traumatomutilla vitelligera +( +Gerstaecker, 1874 +) + +. + + + + +Distribution. + +Traumatomutilla vitelligera + +has been recorded from six South American countries, but we have seen specimens only from semiarid regions of +Ecuador +, +Peru +and +Chile +. + + + + +Remarks. +The vitelligera group is one of the three species groups of +Traumatomutilla +with only one species, + +T. vitelligera +( +Gerstaecker, 1874 +) + +. As in + +T. diabolica +( +Gerstaecker, 1874 +) + +, the mesosomal sculpture of + +T. vitelligera + +differs from other large-bodied +Traumatomutilla +by lacking the distinctive structures of the more diverse, large-bodied species groups [medial longitudinal mesonotal carina (indica), bilobate anterior transverse carina separated from scutellar scale (juvenilis), and lateral mesonotal tubercles (quadrinotata)]. The +lectotype +of + +T. vitelligera + +, however, has a conspicuous scutellar scale connected laterally with its anterolateral carinae, as in many species of the indica group. Additionally, aside from a few species found in northwestern +Colombia +, this is the only species in +Traumatomutilla +known west of the Andes. + + + + \ No newline at end of file diff --git a/data/38/4B/21/384B21D12C9E54318610AD080A03030E.xml b/data/38/4B/21/384B21D12C9E54318610AD080A03030E.xml new file mode 100644 index 00000000000..33068fc66e6 --- /dev/null +++ b/data/38/4B/21/384B21D12C9E54318610AD080A03030E.xml @@ -0,0 +1,962 @@ + + + +Integrative taxonomy of coastal Cafius bistriatus (Erichson) species complex (Coleoptera, Staphylinidae) + + + +Author + +Yoo, In-Seong +https://orcid.org/0000-0002-6720-6025 +Division of Restoration Research, Research Center for Endangered Species, National Institute of Ecology, Yeongyang 36531, Republic of Korea + + + +Author + +Frank, J. H. +Entomology and Nematology Department, University of Florida, Gainesville, FL 32611, USA + + + +Author + +Jung, Jong-Kuen +Department of Biology, Chungnam National University, Daejeon 34134, Republic of Korea + + + +Author + +Ahn, Kee-Jeong +https://orcid.org/0000-0003-4880-0931 +Department of Biology, Chungnam National University, Daejeon 34134, Republic of Korea +kjahn@cnu.ac.kr + +text + + +ZooKeys + + +2022 + +2022-05-12 + + +1100 + + +57 +70 + + + + +http://dx.doi.org/10.3897/zookeys.1100.79435 + +journal article +http://dx.doi.org/10.3897/zookeys.1100.79435 +1313-2970-1100-57 +BCFD1B1880B04CD7A65E2B94DE1B18B5 +5A49A6299089592AB5D77DEF8320BA7D + + + + + +Cafius bistriatus (Erichson) + + + + +Figs 1A +, 2A, D +, 3A, D +, 4 +, 5 + + + + +Philonthus bistriatus +Erichson, 1840: 502. [Type locality: Americae septentrionalis Insula Longa (Long-Island); 1 syntype in MFNB]. + + +Philonthus bilineatus +Erichson, 1840: 503. [Type locality: Americae meridionalis Insula Antiguae, St. Johannis (St. +John's +, the capital of Antigua); 1 syntype in MFNB]. + + +Cafius bistriatus fulgens +Frank, 1986: 153 [in +Frank et al. 1986 +] ( +Cafius +; subspecies of +Cafius bistriatus bistriatus +). [Type locality: Mexico: Baja California Sur: Mulege]. new synonym. See +Herman (2001) +for the detailed synonymy. + + + + +Type +specimens examined. + + + +1 syntype +, "6155 || + +Cafius bilineatus + +| Typus | Er. f. 503. || +Antigua +| Moritz 5.5 || + +Philonthus + +| + +Philonthus bilineatus + +|| = + +Cafius bistriatus + +Er." (MFNB); +1 syntype +, "6152 || + +Cafius bistriatus + +| Typus | Er. f. 502 || Long. 75(2. | Zimmerman | 5.5. || = + +Cafius bilineatus + +Er. | sec. Fauvel || + +Cafius bistriatus + +| Er." (MFNB). + + + + +Other specimens examined. + + + +Canada + +: 6 exx., +Nova Scotia +, + +Cape Breton H. N. P. +Presqu'ile + +, + +3 m + +, +PG562728 +, +13.IX.1984 +\ +J. M. Campbell +& +A. Davies +, sifting beach wrack + +; + +1 ex. +, +Nova Scotia +, +Cape Breton H. N. P. Ingonish N. +Bay, +PG984711 +\ +29.VI.1983 +, +L. LeSage +, LL54 TP18, seashore wrack; 2 exx., +Nova Scotia +, + +Cape Breton H. N. P. +Pleasant Bay + +\ +27.V.1984 +, +L. Masner +, seabeach kelp; 2 exx., +Nova Scotia +, + +Cape Breton H. N. P. +Pleasant Bay + +, seashore kelp\ +29.VII.1983 +, +D.E., J.E. Bright +pans; 4 exx., +N. S. Cape Breton Highl. +N. P. + +25 km +SE Cap Rouge + +, 14.VI.84, +A. Smetana + +; +1 ex. +, C. I.\Schwarz; + +1 ex. +, +New Brunswick +, +Passamaquoddy Bay +, +Pottery Bch. +, +29.VII.1976 +, +M.J. Dadswell + +; + +1 ex. +, +New Brunswick +, +Passamaquoddy Bay +, +Pottery Bch. +, +29.VII.1976 +, +M.J. Dadswell + +; + +1 ex. +, QUE: +St. Adelaide +0.5 mi. + +W. Sandy +Beach Stn. + +, +21.VIII.1953 +, +E.L.Bousfield +; 3 exx., QUE., +4 mi. +S. +Riviėre-a-Claude +, +VII-18-1972 +, 200', +J.M. Campbell +; 5 exx., +N. S. Point Aconi +, +VIII-13-1972 +, +J.M. & BA Campbell +; 5 exx., + +N. S. Big Bras +d'Or + +, +VII-25-1972 +, +J.M. Campbell + +; + +1 ex. +, +Kouchibouguac +N. P., +N. B. +, +1.VI.1977 +, S.J. +Miller +, Code-5195U\ + +Cafius bistriatus + +Er. +Det. J.M. Campbell +1978 + +; +1 ex. +, Kouchibouguac N. P., N. B., +13.IX.1977 +, J.M. Campbell, Code-5953Y. + + +Jamaica + +: 2 exx., JA., +Clarendon +P., + +Jackson's +Bay + +, +12.XII.1972 +, +J. Peck +\Sifting algae on beach; 8 exx., JA., +St. Ann Runaway Bay +, +22.VIII.1974 +, +S. Peck +, beach drift; 10 exx., JA. +St. Catherine +, +7mi. +SE. +Sp. town +, Hellshire Beach, +27.VII.1974 +, +S. Peck +, beach drift + +; + +1 ex. +, JA., +Trelawny Parish +, +Duncans +, VIII.21.1966, +Howden +& +Becker + +. + + +Mexico + +: 6 exx., +Mulege +SEAWEED +Baja Cal. Sur +, +Mex., J +. +Klink Coll., X. +3.66\ERIC; +Scheerpeltz +; 48 exx., +Sonora +, NR. PT. +Cirio +, 29.50-112.40, +28 VIII 1974 +V. Roth Coll +; 163 exx., +Sonora +, +EI Desemboque +, 29.30-112.34, +23 V 1974 +, +Brown +& +Speich +ex flying on beach + +; + +2♂ +2♀ +, +Sonora +, EI +Desembogue +May 23 1974 +Brown +& +Speich + +; + +1 ex. +, +Veracruz Prov. + +8km +S +Veracruz + +, +Hwy +150, +10 July 1990 +J. Ashe +, K-J. +Ahn, R +. +Leschen +ex: under seaweed on beach + +; + +1 ex. +, +Bahia Magdelena +, +1 June 1968 +W. G. Evans +ex; under turtle carapace\SM0038043 KUNHM-ENT + +. + + +USA + +: +1 ex. +, 698., A30 +S. Thomas +, + +Cafius bistriatus + +Er. +S. +Thomas +, coll. + +L.W. +Schaufuss + + +; + +1 ex. +, +Marion +, +Mass. Bowditch. +, + +Cafius bistriatus + +Er. +, +Coll. Schubert + +; + +7♂ +6♀ +( +2♂ +1♀ +dissected, +5♂ +5♀ +in 100% EtOH, AC220), +Puerto Rico +, +Municipio Fajardo +, +Seven Seas Beach +, +18°22.227'N +, +65°38.359'W +, +6 VI 2009 +, +Park +09-021, +JS Park +, +ex +under seaweeds + +; + +4♂ +10♀ +( +1♂ +dissected, +2♂ +9♀ +in 100% EtOH, AC250), +Florida +, +Pinellas Co. +, +Anclote Gulf Park +, +25 X 2008 +, +KJ Ahn +, +JH Ahn +, under seagrasses + +; + +1♂ +5♀ +( +1♂ +dissected, +5♀ +in 100% EtOH), +Florida +, +Brevard Co. +, +Port Canaveral Jetty Park +, +14 II 2009 +, +KJ Ahn +, under stones with empty barnacles; 2 exx., +Florida +Tampa +, +Clearwater Beach +, +10 VI 1995 +, +K.-J. Ahn. +, ex under seaweed; 14 exx. ( +2♂ +dissected, +8 in +100% EtOH), +Florida +, +Cedar Key +, +28 XII 2015 +, +KJ Ahn + +; + +1 ex. +, FLA., +Flamingo +, +Everglades Nat. Pk. +, +4.I.1971 +, +L. Masner + +; + +1 ex. +, CONN, + + +Fairfield Co. +Norwalk + + +, 9 +Aug +78 +Calf Pasture Beach +\ +R.E.Orth +family\ +Wrack-debris +on sandy beach; 2 exx., CONN, + +Fairfield Co. +Westport + +, 11 +Aug +78 + + +Sherwood Is. +St. Pk + + +\ +R.E.Orth +family\ +Wrack-debris +on sandy beach\M3 + +; + +1 ex. +, CONN, + + +Fairfield Co. +Fairfield + + +, 10 +Aug +78 +Jennings Beach +\ +R.E.Orth +family\ +Wrack-debris +on sandy beach; 34 exx. ( +1♂ +dissected, +33 in +100% EtOH), +North Carolina +, +Dare Co. +, +Oregon +Inlet +, +6 IV 2009 +, +KJ Ahn +, +JH Ahn +, under seaweeds; 2 exx., +Cape Cod +, +Massachusetts +, VII.3.1975, +E. J. Kiteley +, under clumps seaweed +Beach + +; +1 ex. +, South Shore S. I., N. Y.\C. L. Pollard, Apr. 11-111, No.; + +1 ex. +, +Portland +Maine +, +July 23 1966 +, +E. J. Kiteley +, dry full carcass + +; +1 ex. +, C. I.\145\Schwarz; +1 ex. +, Md.; + +1 ex. +, +Pt. Isabel +, +Texas +, VI-26-30\JOMartin +Collector +; 2 exx., +Lynn +, +Mass. Essex Co. +V -12; 2 exx., +Lynn +, +Mass. Essex Co + +.; + +1 ex. +, +N.Y. Rockaway +L.I., +15.V.1941 +W. Spector +\ +C.N. +H.M. 1960 +Boris Malkin +Coleoptera +Colln. +; 2 exx., + +Barnegat Bay +NJ + +JW Green +VIII.4.28 \ +C.N. +H.M. 1960 +Boris Malkin +Coleoptera +Colln + +.; + +1 ex. +, +Rocwy Bcb. +L. L + +.; + +1 ex. +, +Peekskill +4/8.80 NY\ +Sherman + +; + +1♀ +\ +Marion Mass. Bowditch. +\ +Cafius bistriatus +Er. +\ex coll. +Scheerpeltz + +\ +Cafius bistriatus +Er.; + +1 ex. +, +TEXAS +: +Wilacy Co. +Port Mansfield +30 September 1990 +J. S. Ashe +ex., beach wrack + +. + + + +Figure 2. +Aedeagi +A, D + +Cafius bistriatus + +B, E + +C. rufifrons + +C, F + +C. sulcicollis + +A-C +lateral aspect +D-F +dorsal aspect. Scale bar: +0.1 mm +. + + + + +Redescription. + +Body medium sized, length 5.5-7.7 mm, forebody length (from clypeus to end of elytron) 3.1-3.7 mm. Body brown to dark brown; head black; metaventrite dark brown to black; anterior part of epipleura usually brighter than elytra. + +Male. +Head + +(Figs +3A +, +4A +). Dull, subquadrate with rounded hind angles, as long as wide (Length/Width = 1.00). Microsculpture reticulate on median, intermediate, and dorso-lateral region; partly coalescent on ventral region; granulate on submentum and gular region. Short longitudinal linelike depression absent on interocular region. Punctures on dorsal surface large and pit-like, median longitudinal impunctate region moderate in size and longitudinal. Seta absent on median region; more or less evenly distributed on intermediate, lateral, and ventral region. Frontoclypeal setiferous puncture, preocular setiferous puncture, lateral ocular setiferous puncture, four occipital setiferous punctures, genal setiferous puncture, and infraorbital setiferous puncture present; interocular setiferous punctures absent; postocular setiferous puncture closer to posterior margin of head than posterior margin of eye. Mentum with two pairs of long setae. Gular sutures completely converged. Dorsal basal carina and nuchal carina present on neck. Antenna (Fig. +4B +) filiform, not short, exceeding posterior margin of head; antennomeres 1-3 very elongate, 4-8 elongate, 9-10 slightly elongate; approximate length ratio of each antennomere 60: 30: 29: 23: 25: 25: 26: 24: 23: 22: 26. Compound eye large, longer than half length of temple (Eye length/Temple length = 0.81-0.86); interfacetal setae very short. +Mouthparts +. Labrum with each lobe moderately transverse, U-shaped; transparent apical membranous part less broad than sclerotized part. Mandibles asymmetrical; blade present, not making small tooth on blade; left and right one both with two internal teeth; 6-7 gland serial pores present. Maxillary palpomere 4 more or less fusiform, narrower than penultimate one. Labial palpomere 3 more or less fusiform; ligula slightly emarginate, seta absent. +Thorax +. Pronotum (Fig. +3D +) glossy on median region, dull on lateral region; rectangular, longer than wide (Length/Width = 1.18-1.19); lateral margin slightly sinuate. Microsculpture indistinctly reticulate on median region; transverse on intermediate region; granulate on lateral region. Disc with homogeneous punctures similar to those of head in size; seta absent on median and intermediate region; densely distributed on lateral region; median impunctate region not clearly defined and not elevated, but depressed series of dorsal setiferous punctures present on midline forming 2 longitudinal rows, each with about 20 punctures, not separated distinctly from ground punctures; largest setiferous lateral puncture separated from lateral carina by at least 3 times width of the puncture. Prosternum (Fig. +4C +) with 2 long macrosetae on central region; sternacostal carina making angle posteriorly. Hypomeron with distinct microsculpture but seta absent. Elytra (Fig. +4F +) long (Length/Width = 2.25-2.42), longer than pronotum at midline (Elytron length/Pronotum length = 1.42-1.50), wider than pronotum in maximum width (Elytra width/Pronotum width = 1.41-1.53); one subhumeral seta present but lateral seta absent; punctation simple and dense. Mesoventrite (Fig. +4G +) with transverse carina connected to lateral margins of mesoventral process; mesoventral process more or less pointed; mesocoxal cavities narrowly separated, posterior margin completely developed. Front tibia (Fig. +4D +) with several spines; front tarsomeres 1-4 (Fig. +4E +) strongly dilated laterally, tarsomere 5 broadened apically, pale setae slightly spatulate; hind tarsomere 1 longer than 5. +Abdomen +. Microsculpture reticulate on tergites (Fig. +4H +); punctures more or less coalescent; pubescence on each tergite more or less longitudinally directed. Posterior margin of segments III-VI straight. Posterior transverse basal carina complete on tergites III-VI, absent on tergite VII. Pubescence of segment VIII much sparser than segment VII. Tergite VIII (Fig. +5A +) with 2 long macrosetae present on each side of midline, apical margin arcuate. Laterotergal sclerite (Fig. +5D +) long and slender, with 5 long macrosetae and 2 long macrosetae on tip. Posterior margin of tergite X emarginate apically, apical portion pigmented. Apical setae of tergite X present. Basal carina on sternite III rounded. Sternite VIII (Fig. +5B +) with 3 long macrosetae on each side of midline, apical margin deeply emarginate. Basal part of sternite IX (Fig. +5C +) well developed, asymmetrical; posterior margin of sternite IX emarginate. +Aedeagus +(Fig. +5H, I +) Apical process of median lobe abruptly narrowed on ventral aspect, not constricted in apical third. Paramere longer than half length of median lobe; apical region rounded on ventral aspect; about 7 acorn-shaped pegs present on apico-medial region, forming more or less 2 rows; 4 apical and 2 pairs of lateral setae present on margin, apical setae separated from lateral setae, all setae similar in length. +Female. +Apical margin of abdominal sternite VIII (Fig. +5E +) entire, rounded; gonocoxite II narrowly tubular (Fig. +5F +); gonostyle with 1 long macroseta on tip, separated from gonocoxite II and sclerotized. Tergite X as in Fig. +5G +. + + + +Figure 3. +SEM photographs +A, D + +Cafius bistriatus + +B, E + +C. rufifrons + +C, F + +C. sulcicollis + +A-C +head, dorsal aspect +D-F +pronotum, dorsal aspect. + + + + +Distribution. +Canada, USA (Pacific and Atlantic coasts), Mexico, West Indies, Venezuela. + + +Figure 4. + +Cafius bistriatus + +A +head, ventral aspect +B +antenna +C +prosternum, ventral aspect +D +front tibia, lateral aspect +E +front tarsus, dorsal aspect +F +elytron, dorsal aspect +G +meso- and metaventrites, ventral aspect +H +abdomen, dorsal aspect. + + + + +Remarks. + +Members of the + +Cafius bistriatus + +species complex ( + +C. bistriatus + +, + +C. rufifrons + +, and + +C. sulcicollis + +) are very similar in external form and internal structure and so they could be treated as cryptic species. A comparison table of morphological characters among + +C. bistriatus + +, + +C. rufifrons + +, and + +C. sulcicollis + +is presented in Table +3 +. + + + +Figure 5. + +Cafius bistriatus + +A +male tergite VIII, dorsal aspect +B +male sternite VIII, ventral aspect +C +male sternite IX, ventral aspect +D +male lateroteral sclerite and tergite X, dorsal aspect +E +female sternite VIII, ventral aspect +F +gonocoxite, ventral aspect +G +female tergite X, dorsal aspect +H +aedeagus, dorsal aspect +I +aedeagus, lateral aspect. Scale bar: 0.1 mm. + + + + + + \ No newline at end of file diff --git a/data/38/4B/4B/384B4BC087D306A520D7E99E393FA97A.xml b/data/38/4B/4B/384B4BC087D306A520D7E99E393FA97A.xml new file mode 100644 index 00000000000..96b46810fba --- /dev/null +++ b/data/38/4B/4B/384B4BC087D306A520D7E99E393FA97A.xml @@ -0,0 +1,792 @@ + + + +Info Flora Schweiz - Poaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/poaceae.html + +url + + + + + +Alopecurus geniculatus +L. + + + + + +Geknieter Fuchsschwanz + + + + +Art ISFS: 25700 Checklist: 1002900 +Poaceae +Alopecurus +Alopecurus geniculatus L. + + + +Bestimmungsschluessel + + + +Zusammenfassung + + + + +Artbeschreibung + +(nach +Lauber & al. 2018 +) + +: +Staengel +10-40 cm +, +bueschelig +, +niederliegend und an den Knoten wurzelnd +, oft im Wasser flutend, knickig aufsteigend. +Blatthaeutchen +bis +5 mm +lang. Oberste Blattscheide etwas aufgeblasen. + +Bluetenstand +dicht +aehrig-zylindrisch +, +2-5 cm +lang und ca. +5 mm +dick + +. +Aehrchen +einbluetig +, ca. +3 mm +lang. +Huellspelzen +nur am Grund verwachsen, stumpf, ganzer Kiel behaart. Deckspelze so lang wie die +Huellspelzen +. Granne gekniet, dem Grund der Spelze entspringend und diese um ca. +2 mm +ueberragend +. + + + + +Bluetezeit + +(nach +Lauber & al. 2018 +) + +: 5-9 + + +Standort und Verbreitung in der Schweiz + +(nach +Lauber & al. 2018 +) + +: Periodisch +ueberschwemmte +Boeden +, nasse, +geduengte +Wiesen / kollin-subalpin / CH + + + + +Verbreitung global + +(nach +Lauber & al. 2018 +) + +: Eurosibirisch + + + + +Oekologische +Zeigerwerte + +(nach +Landolt & al. 2010 +) + +4 + w + 33+43 + 3.k.2n=28 + + + +Status + + + +Status IUCN +: Verletzlich + + + + +Nationale +Prioritaet +: 4 - +Maessige +nationale +Prioritaet + + +Internationale Verantwortung +: 1 - Gering Erhalten/ +Foerdern +Gefaehrdungen +Zunahme Konkurrenz an +naehrstoffreicheren +Standorten +Abbautaetigkeit +und Sukzession in Kiesgruben Verschwinden oder +Beeintraechtung +der +Lebensraeume +( +Rueckgang +von periodisch +ueberfluteten +Mulden (astatische +Gewaesser +) und Wiesen, +vernaesste +Mulden, Pionierstellen, +Soelle +) Verlust des Lebensraums ( +Rueckgang +von periodisch +ueberfluteten +Mulden (astatische +Gewaesser +) und Wiesen) Isolierte Restpopulationen Anatomie + + +Zusammenfassung +der Blattanatomie Obere Epidermiszellen gleich gross wie untere. Epidermis mit Papillen. +Leitbuendel +freistehend. +Leitbuendelhuelle +verholzt. + + +Zusammenfassung der Stammanatomie + + +Umriss rund oder oval. +Leitbuendel +in einer Reihe. Kleine Interzellularen, oft dreieckig. Epidermiszellen verholzt. Kontinuierlicher +Chlorenchyma-Guertel +aus unverholzten Zellen. + + +Beschreibung (Englisch) + + +Culm-diameter +1-2 mm +, wall large, radius of culm in relation to wall thickness 1:0.5. Outline circular with a smooth surface. Culm-center hollow and surrounded by many large thin-walled, not lignified cells. Epidermis-cells thick-walled all around. Large vascular bundles arranged in 2-3 peripheral rows. Chlorenchyma in tangentially enlarged groups. Sclerenchyma in a small, peripheral continuous belt (<4 cells). Cells thick-walled. Small sclerenchymatic sheath with 1-2 cells around vascular bundles. Largest vessels in vascular bundles in lateral position. Largest vessel in the bundle 20-50 +μm +. Cavities (intercellulars) between parenchyma-cells present, small, often triangular. + + + +Oekologie + + +Lebensform Monokarper Hemikryptophyt + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + + + + + +
+7.1.1 - Feuchte Trittflur ( +Agropyro-Rumicion +) +
+
+ + +fett + +Dominante Art, welche das Aussehen des Lebensraumes +mitpraegt + +Charakterart +Weniger strikt an den Lebensraum gebundene Art + + +
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +nass; Feuchtigkeit stark wechselnd (mehr als ++/- +2 Stufen) +Lichtzahl LhellSalzzeichen1
Reaktionszahl Rschwach sauer bis neutral (pH 4.5-7.5)Temperaturzahl Tunter-montan und ober-kollin
+Naehrstoffzahl +N + +maessig +naehrstoffarm +bis +maessig +naehrstoffreich + +Kontinentalitaetszahl +K + +subozeanisch bis subkontinental (mittlere Luftfeuchtigkeit, +maessige +Temperaturschwankungen und +maessig +tiefe Wintertemperaturen) +
+
+
+ + +Abhaengigkeit +vom Wasser + + + + + + + + + + + + + + + + + +
+Fluesse +1 - Zusatz- oder Nebenlebensraum
Ruhiges Wasser1 - Zusatz- oder Nebenlebensraum
Grundwasser0 - unbedeutend, keine Bindung.
+
+ +Nomenklatur + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Alopecurus geniculatus +L. + + +
+ + +Volksname Deutscher Name: +Geknieter Fuchsschwanz +Nom +francais +: + +Vulpin +genouille + +Nome italiano: +Coda di topo ginocchiata + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Alopecurus geniculatus L. + + +Checklist 2017 + +25700
= +Alopecurus geniculatus L. + + +Flora Helvetica 2001 + +2787
= +Alopecurus geniculatus L. + + +Flora Helvetica 2012 + +2967
= +Alopecurus geniculatus L. + + +Flora Helvetica 2018 + +2967
= +Alopecurus geniculatus L. + + +Index synonymique 1996 + +25700
= +Alopecurus geniculatus L. + + +Landolt 1977 + +215
= +Alopecurus geniculatus L. + + +Landolt 1991 + +200
= +Alopecurus geniculatus L. + + +SISF/ISFS 2 + +25700
= +Alopecurus geniculatus L. + + +Welten & Sutter 1982 + +2325
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Status Indigenat +: Indigen + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein + + +Status Rote Liste national 2016 + + +Status IUCN +: Verletzlich + + + +Zusaetzliche +Informationen + +Kriterien IUCN: A3c; B2ab(iii) + + +Status Rote Liste regional 2019 + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Biogeografische RegionenStatusKriterien IUCN
Jura (JU)verletzlich (Vulnerable)A3c; B2ab(iii)
Mittelland (MP)verletzlich (Vulnerable)A3c; B2ab(iii)
Alpennordflanke (NA)verletzlich (Vulnerable)A3c; B2ab(iii)
+Alpensuedflanke +(SA) +verletzlich (Vulnerable)B2ab(iii)
+Oestliche +Zentralalpen (EA) +verletzlich (Vulnerable)B2ab(iii)
Westliche Zentralalpen (WA)verletzlich (Vulnerable)B2ab(iii)
+
+ + +Status nationale +Prioritaet +/Verantwortung + + + + + + + + + + + + + + + + + + + + + + +
+ +Nationale +Prioritaet + + +4 - +Maessige +nationale +Prioritaet +
+Massnahmenbedarf + +1 - +Moeglicher +(unsicherer) Massnahmebedarf +
+ +Internationale Verantwortung + +1 - Gering
+ +Ueberwachung +Bestaende + + +0 - +Ueberwachung +ist nicht +noetig +
+
+ +Schutzstatus + + + + + + + + + + + + + + + + + + + +
+International (Berner Konvention) +Nein
+GE + +Vollstaendig +geschuetzt +(25.07.2007)
+NW + +Vollstaendig +geschuetzt +(29.11.2005)
+
+ + + + + + + + + + + + + +
+Schweiz +--
+VD + +Vollstaendig +geschuetzt +(02.03.2005)
+
+Status in sektoriellen Umweltpolitiken + + + + + + + +
+Umweltziele Landwirtschaft: +Z - Zielartweitere Informationen
+
+
+ + +Erhalten/ +Foerdern +Gefaehrdungen +und Massnahmen Zunahme Konkurrenz an +naehrstoffreicheren +Standorten Extensive Beweidung oder Mahd +foerdern +Abbautaetigkeit +und Sukzession in Kiesgruben Informieren der Betreiber, Markieren mit Bitte um Information (z.B. an die Stiftung Landschaft und Kies im Kanton Bern), falls Massnahmen am Fundort geplant Vor einem Abbau Pflanzen an andere geeignete Standorte in derselben Grube umsiedeln Verschwinden oder +Beeintraechtung +der +Lebensraeume +( +Rueckgang +von periodisch +ueberfluteten +Mulden (astatische +Gewaesser +) und Wiesen, +vernaesste +Mulden, Pionierstellen, +Soelle +) Neuschaffung von feuchten und +regelmaessig +gestoerten +Stellen +Foerderung +von lang andauernden +Ueberflutungen +, in den Trockenphasen +maehen +oder extensiv beweiden, zur Reduktion von Konkurrenten (Schilf etc.) +Foerdern +von Pionierstellen durch Bodenabtrag Verlust des Lebensraums ( +Rueckgang +von periodisch +ueberfluteten +Mulden (astatische +Gewaesser +) und Wiesen) +Foerderung +von lang andauernden +Ueberflutungen +, in den Trockenphasen +maehen +oder extensiv beweiden, zur Reduktion von Konkurrenten (Schilf etc.) +Foerdern +von Pionierstellen durch Bodenabtrag Isolierte Restpopulationen Die Populationen sollten in ein +regelmaessiges +Monitoringprogramm aufgenommen werden (zum Beispiel mit Pflanzenpatenschaften) Ex-situ Kulturen und Ansiedlungen oder Wiederansiedlungen in Gebieten mit erloschenen Vorkommen Lagern der Samen in einer nationalen Samenbank Ex situ Material Close + + +
+
\ No newline at end of file diff --git a/data/38/4B/86/384B86B81597909593EB533F76EA952C.xml b/data/38/4B/86/384B86B81597909593EB533F76EA952C.xml new file mode 100644 index 00000000000..a84e4915e99 --- /dev/null +++ b/data/38/4B/86/384B86B81597909593EB533F76EA952C.xml @@ -0,0 +1,97 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part T) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +878 +905 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Tillandsia polystachia +(Linnaeus) Linnaeus + +, + +Species Plantarum +, ed. 2, 1 + +: 410. 1762 + + +. + + + +"Habitat in America calidiore." RCN: 22771 + + + +Basionym: + +Renealmia polystachia +L. (1753) + +. + + + + + +Neotype + +(Smith & Downs, +Fl. Neotropica +14: 924. 1977): +Plumier, s.n. +(P). + + + + +Current name: + + +Tillandsia polystachia + +(L.) L. + +( +Bromeliaceae +). + + + + \ No newline at end of file diff --git a/data/38/4B/87/384B87EBFFA7FFDFFEF9FB09F7AC454D.xml b/data/38/4B/87/384B87EBFFA7FFDFFEF9FB09F7AC454D.xml new file mode 100644 index 00000000000..4087d0750ba --- /dev/null +++ b/data/38/4B/87/384B87EBFFA7FFDFFEF9FB09F7AC454D.xml @@ -0,0 +1,161 @@ + + + +New species of the genus Hyleoglomeris from Korea (Diplopoda: Glomerida: Glomeridae) + + + +Author + +Mikhaljova, Elena V. + + + +Author + +Lim, Kil-Young + +text + + +Zootaxa + + +2006 + +1224 + + +45 +58 + + + +journal article +10.5281/zenodo.172637 +f8158bf1-bb55-4ec9-aa5f-08a093c9032c +1175­5326 +172637 + + + + + + + +Hyleoglomeris alutacea +Mikhaljova & Lim + +, +sp. n. + + + + +Figs 30–37 +. + + + + +Material examined + + + +Holotype + +: +1 male +(ChNU), from Gyorye, Jeju­do, +South Korea +, collected +3 June1992 +by K.­Y. Lim. + +Paratypes + +: +4 males +, +3 females +(ChNU), +1 male +, +1 female +( +ZMUM +), same locality as for +holotype +, collected +3 June 1992 +by K.­Y. Lim. + + + + +Diagnosis + +Differs from congeners mainly by the shagreen striate portion of the thoracic shield and the thoracic coloration pattern of an anterior white­yellowish narrow transverse band and pair of marbled brown oblong lateral spots, combined with the subovoid syncoxital lobe of the telopods, the very high telopod syncoxital horn with subapical setigerous processes and the small coxal lobe of male leg pair 17. + + + +Etymology + +The specific epithet refers to the shagreen striate portion of the thoracic shield. + + + +Description + + +Male. Length +4.5–5.5 mm +, width 2.5–3.0 mm. Background coloration of head brown with several small light spots between and above antennal sockets; clypeus, labrum and Tömösváry’s organs yellow. Ocelli black. Antennae brown; antennomeres 1 and 2 light brown. Dorsum brown. Collum with a large oval marbled brown central spot ( +Fig. 30 +). Thoracic shield with a white­yellowish narrow transverse band; pair of marbled brown oblong spots placed laterally ( +Fig. 31 +). Each following tergite with pair of marbled brown lateral spots and a translucid caudal margin ( +Fig. 32 +). Hidden anterior portion of tergite brown. Pigidium brown with a lucid caudal margin but without any pattern. Venter yellowish. Legs yellowish with light brown distal and dorsal portions. Telopods yellowish. + + +Ocelli convex, 6+1 on each side of head. Antennomere 6 about 2.0 time longer than wide. Dorsum smooth. Collum semicircular, with two transverse striae. Thoracic shield with 9­10 delicate striae, of which only three entirely crossing dorsum; lateral striate portion shagreen. Length of the striae varied. As usual, anterior border of thoracic shield with one stria concealed under caudal margin of collum. Hyposchism relatively narrow, reaching but not protruding beyond caudal tergal margin. Anterolateral corners of hyposchism rounded and somewhat protruding anteriad ( +Fig. 31 +). A broad hollow occupying 4–5 striae placed between schism and hyposchism laterally. Pigidium very indistinctly sinuate medially at caudal margin. + + +Leg pair 17 ( +Fig. 33 +) with small and irregularly rounded outer coxal lobes, telopodite 4­segmented with three or four claws apically. Leg pair 18 ( +Fig. 34 +) with a lancet­shaped syncoxital notch; telopodite 4­segmented. + + + +FIGURES 30–37. + +Hyleoglomeris alutacea + + +sp. n. + +, paratype male: 30, colour pattern on collum; 31, colour pattern on thoracic shield; 32, colour pattern on a midbody tergite; 33, leg 17; 34, leg 18; 35, telopods, frontal view; 36, apex of telopod syncoxital horn; 37, distal part of telopod, caudal view. Scales in mm. + + + +Telopods with a small thick subovoid microsetose central syncoxital lobe having a low smooth prominence frontally and shagreen shallow cavity caudally ( +Fig. 35 +). Syncoxital lateral horns very high, slender, directed caudad, covered with setae proximally. Distal portion of the syncoxite horn with subapical curved setigerous processes caudally ( +Fig. 36 +). Prefemur micropapillate laterally and somewhat mesally, with a long inner setose finger crowned with a long flagelloid. Femur with a shorter anteromesal setose finger also crowned by a flagelloid and posteriorly with a large inner outgrowth apically bearing a membranous sack curved forward. Caudomedial outgrowth of femur narrow at base ( +Fig. 37 +). Tibia with a long anteromedial seta, posteriorly with a medial outgrowth strongly curved anteriad. Caudomedial outgrowth of tibia with a micropapillate tubercle at base. Tarsus with strongly curved caudad distal part and a subapical seta. + + +Female. Length 6.0–7.0 mm, width 3.0– +3.5 mm +. Pigidium regularly margined. Ocelli 6+1 on each side of head. Thoracic shield with 9–10 delicate striae, of which only three entirely crossing dorsum; lateral striate portion shagreen. Length of the striae varied. A broad hollow occupying 4–5 striae placed between schism and hyposchism laterally. + + + + \ No newline at end of file diff --git a/data/38/4B/87/384B87EBFFA9FFDDFEF9FD4EF1D84203.xml b/data/38/4B/87/384B87EBFFA9FFDDFEF9FD4EF1D84203.xml new file mode 100644 index 00000000000..75ba23aec06 --- /dev/null +++ b/data/38/4B/87/384B87EBFFA9FFDDFEF9FD4EF1D84203.xml @@ -0,0 +1,193 @@ + + + +New species of the genus Hyleoglomeris from Korea (Diplopoda: Glomerida: Glomeridae) + + + +Author + +Mikhaljova, Elena V. + + + +Author + +Lim, Kil-Young + +text + + +Zootaxa + + +2006 + +1224 + + +45 +58 + + + +journal article +10.5281/zenodo.172637 +f8158bf1-bb55-4ec9-aa5f-08a093c9032c +1175­5326 +172637 + + + + + + + +Hyleoglomeris confragosa +Mikhaljova & Lim + +, +sp. n. + + + + +Figs 22–29 +. + + + + +Material examined + + + +Holotype + +: +1 male +(ChNU) from Jeongok, Yeonchon­gun, Gyeongi­do, +South Korea +, collected +17 May 1991 +by K.­Y. Lim. +Parartype +: +1 female +(ChNU), same locality as for +holotype +, collected +17 May 1991 +by K.­Y. Lim. + + + + +Diagnosis + +Differs from congeners mainly by the thoracic coloration pattern of the anterior whiteyellowish transverse band and pair of marbled brown oblong lateral spots, combined with the oval, vertically stretched syncoxital lobe of the telopods, the very high telopod syncoxital horns without apical modifications, the strongly curved anteriad caudotibial outgrowths of the telopods, the irregularly rounded edge of the small coxal lobe of the male leg pair 17. + + + + + + + + + + + + + + + + + + + + + + + + +
+Etymology +
The specificepithet referstothe irregularlyroundededgeofthecoxallobeofmaleleg
pair 17.
+
+ + +Description + + +Male. Length +5.5 mm +, width +2.9 mm +. Background coloration of head brown with several small light spots between and above antennal sockets; clypeus, labrum and Tömösváry’s organs yellow. Ocelli black. Antennae dark­brown; antennal sockets yellow. Dorsum brown. Collum with a large oval marbled brown central spot ( +Fig. 22 +). Thoracic shield with a white­yellowish transverse band occupying its anterior striate portion; pair of marbled brown oblong spots placed laterally ( +Fig. 23 +). Each following tergite with pair of marbled brown oblong lateral spots and a translucid caudal margin ( +Fig. 24 +). Hidden anterior portion of tergite marbled brown. Pigidium brown with lucid caudal margin and without any pattern. Venter, legs and telopods yellowish. + + +Ocelli convex, 6+1 on each side of head. Antennomere 6 about 2.0 time longer than wide. Dorsum smooth. Collum semicircular, with two transverse striae. Thoracic shield with 9 delicate striae of which only three entirely crossing dorsum, with a relatively narrow hyposchism reaching but not protruding beyond caudal tergal margin. Anterolateral corners of hyposchism lobe­shaped and protruding anteriad ( +Fig. 23 +). Length of stria varied. A broad hollow occupying 4 striae placed between schism and hyposchism laterally. As usual, anterior border of thoracic shield with one stria concealed under caudal margin of collum. Pigidium delicately sinuate medially at caudal margin. + + + +FIGURES 22–29. + +Hyleoglomeris confragosa + + +sp. n. + +, holotype male: 22, colour pattern on collum; 23, colour pattern on thoracic shield; 24, colour pattern on a midbody tergite; 25, leg 17; 26, leg 18; 27, telopods, frontal view; 28, apex of telopod syncoxital horn; 29, distal part of telopod, caudal view. Scales in mm. + + + +Leg pair 17 ( +Fig. 25 +) with small and irregularly rounded outer coxal lobes, telopodite 4­segmented with three claws apically. Leg pair 18 ( +Fig. 26 +) with a lancet­shaped syncoxital notch; telopodite 4­segmented. + + +Telopods ( +Fig. 27 +) with a relatively small, thick, oval, vertically stretched, microsetose central syncoxital lobe. Surface of syncoxital lobe with a low smooth prominence frontally and shagreen shallow cavity caudally. Syncoxital lateral horns very high, slender, covered with setae proximally. Distal portion of syncoxital horn without visible modifications, excluding tiny wrinkles ( +Fig. 28 +). Prefemur micropapillate laterally and somewhat mesally, with a long inner setose finger crowned with a long flagelloid. Femur with a shorter antero­mesal setose finger also crowned with a flagelloid and posteriorly with a large inner outgrowth apically bearing a membranous sack curved forward. Caudomedial outgrowth of femur wide at base ( +Fig. 29 +). Tibia with a long anteromedial seta, posteriorly with medial outgrowth strongly curved anteriad. Caudomedial outgrowth of tibia bearing a micropapillate tubercle. Tarsus with a strongly curved caudad distal part and a subapical seta. + +Female. Length 7.0 mm, width 3.0 mm. Pigidium regularly margined. Ocelli 6+1 on each side of head. Thoracic shield with 10 delicate striae on left side and 11 such striae on right side, of which only three entirely crossing dorsum. Length of the striae varied. A broad hollow occupying 4 striae placed between schism and hyposchism. + + + +Remarks + + +A restudy of the above material proves that +Mikhaljova & Lim (2000) +misidentified + +Hyleoglomeris confragosa + + +sp. n. + +specimens (male and female) from Gyeongi­do, +South Korea +as belonging to + +H. koreana +. + + + +
+
\ No newline at end of file diff --git a/data/38/4B/87/384B87EBFFABFFD3FEF9FE74F2D64445.xml b/data/38/4B/87/384B87EBFFABFFD3FEF9FE74F2D64445.xml new file mode 100644 index 00000000000..dbf5e0d898e --- /dev/null +++ b/data/38/4B/87/384B87EBFFABFFD3FEF9FE74F2D64445.xml @@ -0,0 +1,174 @@ + + + +New species of the genus Hyleoglomeris from Korea (Diplopoda: Glomerida: Glomeridae) + + + +Author + +Mikhaljova, Elena V. + + + +Author + +Lim, Kil-Young + +text + + +Zootaxa + + +2006 + +1224 + + +45 +58 + + + +journal article +10.5281/zenodo.172637 +f8158bf1-bb55-4ec9-aa5f-08a093c9032c +1175­5326 +172637 + + + + + + + +Hyleoglomeris obscura +Lim + +, +sp. n. + + + + +Figs 15–21 +. + + + + +Material examined + + + +Holotype + +: +1 male +(ChNU) from Jeongok, Yeonchon­gun, Gyeongi­do, +South Korea +, collected +17 May 1991 +by K.­Y. Lim. + + + + +Diagnosis + +Differs from congeners mainly by the coloration pattern of dorsum with pair of indistinct, weakly marbled black­brown oval lateral spots on each tergite as well as with a yellowish, wide transverse band interrupted centrally on the thoracic shield, combined with the syncoxital lobe of the telopods being relatively large and rounded apically, the telopod syncoxital horns devoid of apical modifications, the caudotibial outgrowths of the telopods strongly curved anteriad, the shape of the syncoxital notch (as vertical section of a crater) of male leg pair 18. + + + + + + + + + + + + + + + + + + + + + +
+Etymology +
The specific epithet referstotheblack­browncolorationofthedorsumwithindistinct,
weakly marbled, lateral spots.
+
+ + +Description + + +Male. Length 9.0 mm, width +4.5 mm +. Background coloration of head black­brown; clypeus, labrum and Tömösvary’s organs light brown. Ocelli black. Antennae brown with black­brown distal parts. Dorsum black­brown. Collum with a large vague, oval marbled brown central spot ( +Fig. 15 +). Thoracic shield with a yellowish wide transverse band occupying its anterior portion and somewhat widening laterad; the band interrupted centrally as a narrow stripe; pair of indistinct weakly marbled black­brown oval spots placed laterally ( +Fig. 16 +). Each following tergite with pair of relatively indistinct weakly marbled black­brown oval lateral spots and a translucid caudal margin ( +Fig. 17 +). Hidden anterior portion of tergite weakly marbled brown or black­brown. Pigidium black­brown, without any pattern. Venter yellowish, with brownish sternites. Distal parts of legs brownish, growing increasingly dark distad. Leg coxae brown apically. Coxal lobes of leg pair 17 brownish. Telopods brownish laterally. + +Ocelli convex, 9+1 on each side of head. Antennomere 6 about 2.1–2.2 times longer than wide. Dorsum smooth. Collum semicircular, with two transverse striae. Thoracic shield with a relatively narrow hyposchism reaching but not protruding beyond hind tergal margin, with 7 delicate striae of which only three entirely crossing dorsum. Length of the striae varied. As usual, anterior border of thoracic shield with one stria concealed under caudal margin of collum. Pigidium delicately sinuate medially at caudal margin. + +Leg pair 17 ( +Fig. 18 +) with high and regularly rounded outer coxal lobes, telopodite 4­ segmented with three claws apically. Leg pair 18 ( +Fig. 19 +) with syncoxital notch as vertical section of a crater, telopodite 4­segmented. + + + +FIGURES 15–21. + +Hyleoglomeris obscura + + +sp. n. + +, holotype male: 15, colour pattern on collum; 16, colour pattern on thoracic shield; 17, colour pattern on a midbody tergite; 18, leg 17; 19, leg 18; 20, telopods, frontal view; 21, distal part of telopod, caudal view. Scales in mm. + + + +Telopods ( +Fig. 20 +) with a relatively large subovoid, horizontally stretched, central syncoxital lobe covered with microscopic hairs, curved anteriad. Surface of syncoxital lobe smooth frontally and shagreen caudally. Syncoxital lateral horns high, slender, directed strongly caudoventrad, covered with setae laterally but not mesally. Distal portion of syncoxital horns without modifications. Prefemur micropapillate laterally and mesally, with a long inner setose finger crowned with a long flagelloid. Femur with a shorter anteromesal setose finger also crowned with a flagelloid and posteriorly with a large inner outgrowth apically bearing a membranous sack curved forward. Caudomedial outgrowth of femur wide at base ( +Fig. 21 +). Tibia with a long anteromedial seta, posteriorly with medial outgrowth strongly curved anteriad. Caudomedial outgrowth of tibia with a weakly micropapillate tubercle at base. Tarsus with a strongly curved caudad distal part and a subapical seta. + +Female unknown. + + + +Remarks + + +A restudy of the above material proves that +Mikhaljova & Lim (2000) +misidentified the male of + +Hyleoglomeris obscura + + +sp. n. + +from Gyeongi­do, +South Korea +as belonging to + +H. koreana + +. + + +
+
\ No newline at end of file diff --git a/data/38/4B/87/384B87EBFFACFFD1FEF9F9B3F2C3478D.xml b/data/38/4B/87/384B87EBFFACFFD1FEF9F9B3F2C3478D.xml new file mode 100644 index 00000000000..fc70ee7b80c --- /dev/null +++ b/data/38/4B/87/384B87EBFFACFFD1FEF9F9B3F2C3478D.xml @@ -0,0 +1,199 @@ + + + +New species of the genus Hyleoglomeris from Korea (Diplopoda: Glomerida: Glomeridae) + + + +Author + +Mikhaljova, Elena V. + + + +Author + +Lim, Kil-Young + +text + + +Zootaxa + + +2006 + +1224 + + +45 +58 + + + +journal article +10.5281/zenodo.172637 +f8158bf1-bb55-4ec9-aa5f-08a093c9032c +1175­5326 +172637 + + + + + + + +Hyleoglomeris buana +Lim + +, +sp. n. + + + + +Figs 7–14 +. + + + + +Material examined + + + +Holotype + +: +1 male +(ChNU) from Buan­gun, Jeollabuk­do, +South Korea +, collected +18 May 1991 +by K.­Y. Lim. + +Paratypes + +: +1 male +, +1female +(ChNU), +1 male +( +ZMUM +), same locality as for +holotype +, collected +18 May 1991 +by K.­Y. Lim. + + + + +Diagnosis + +Differs from congeners mainly by the syncoxital lobe of the telopods being relatively large, subovoid and stretched horizontally, by the high telopod syncoxital lateral horn supplied with a subapical setoid, as well as by the coloration pattern of a white, wide, unbroken, widened laterad belt on the thoracic shield and of pair of marbled brown oblong lateral spots on each following tergite. + + + +Etymology + + +The specific epithet refers to the +type +locality. + + + + +Description + + +Male. Length ca.8.0 mm, width +3.5–3.7 mm +. Background coloration of head blackbrown with several small yellowish­white spots above level of antennal sockets; clypeus and labrum yellowish­white. Antennae brown; antennomeres 1 and 2 light brown. Tömösváry’s organs white. Ocelli black. Dorsum black­brown. Collum with a marbled brown central pattern ( +Fig. 7 +). Thoracic shield with a white, wide, unbroken transverse belt occupying its anterior portion and widening laterad ( +Fig. 8 +). Each following tergite with pair of marbled brown oblong lateral spots and a translucid caudal margin. Hidden anterior portion of the tergite marbled brown. Pigidium black­brown with a white caudal margin and five indistinct, small, subtriangular central spots near somite 11. Some specimens with very weak traces of an axial stripe on posterior 3–4 somites. Venter white. Distal parts of legs brownish. Telopods white. + + +Ocelli convex, gradually reducing in size toward Tömösváry’s organ. +Holotype +with 9+1 ocelli and +paratypes +with 8+1 or 9+1 ocelli on each side of head. Antennomere 6 about 2.1–2.2 times longer than wide. Dorsum smooth. Collum with two transverse striae. Thoracic shield with a relatively narrow hyposchism reaching but not protruding beyond hind tergal margin, with 9 delicate striae of which only four entirely crossing dorsum ( +Fig. 9 +). Length of the striae varied. As usual, anterior border of thoracic shield with one stria concealed under caudal margin of collum. Pigidium delicately sinuate medially at caudal margin. + + +Leg pair 17 ( +Fig. 10 +) with high, regularly rounded outer coxal lobes, telopodite 4­ segmented. Leg pair 18 ( +Fig. 11 +) with a lancet­shaped syncoxital notch, telopodite 4­ segmented, basal segment with rare papillae laterally. + + +Telopods ( +Fig. 12 +) massive; central lobe of syncoxite relatively large, subovoid, stretched horizontally, covered with microscopic hairs, very weakly curved anteriad. Surface of syncoxital lobe smooth frontally and shagreen caudally. Syncoxital lateral horns high, slender, setose, directed somewhat caudoventrad, each with a setoid subapically ( +Fig. 13 +). Prefemur micropapillate laterally and mesally. Prefemur with a long inner setose finger crowned with a long flagelloid. Femur with a shorter anteromesal setose finger also crowned by a flagelloid, posteriorly with a large inner outgrowth apically bearing a membranous sack curved forward. A small papillate field at base of femoral anteromesal finger. Caudomedial outgrowth of femur relatively narrow at base ( +Fig. 14 +). Tibia with a long anteromedial seta, posteriorly with a curved, dentiform, medial outgrowth. Caudomedial outgrowth of tibia with a weakly micropapillate tubercle at base. Tarsus with a somewhat curved caudad distal part and a strong subapical seta. + +Female. Length 8.0 mm, width 4.0 mm. Ocelli 9+1 on right side of head, 8+1 on left side of head. Antennae reduced, deformed. Pigidium regularly margined. + + + +FIGURES 7–14. + +Hyleoglomeris buana + + +sp. n. + +, paratype male: 7, colour pattern on collum; 8, colour pattern on dorsum; 9, left lateral side of thoracic shield; 10, leg 17; 11, leg 18; 12, telopods, frontal view; 13, apex of telopod syncoxital horn; 14, distal part of telopod, caudal view. Scales in mm. + + + + +Remarks + + +A restudy of the above material from +South Korea +, which was misidentified as + +Hyleoglomeris emarginata +Golovatch, 1981 + +by +Mikhaljova & Lim (2000) +proves that it actually belongs to + +H. buana + +sp. n. +Thus, at present only six species of + +Hyleoglomeris + +(including new species) definitely occur in +Korea +. + + +This new species seems to be particularly closely related to + +H. koreana +Golovatch, 1978 + +described from the environs of Kannyn, +South Korea +, but differs by the shape of the caudomedial outgrowth of the telopod femur, by the structure of syncoxital lobe and lateral horns of the telopods, as well as by arrangement of thoracic striae and body coloration. + + + + \ No newline at end of file diff --git a/data/38/4B/87/384B87EBFFAFFFD6FEF9FE24F66647FD.xml b/data/38/4B/87/384B87EBFFAFFFD6FEF9FE24F66647FD.xml new file mode 100644 index 00000000000..eb72673b591 --- /dev/null +++ b/data/38/4B/87/384B87EBFFAFFFD6FEF9FE24F66647FD.xml @@ -0,0 +1,144 @@ + + + +New species of the genus Hyleoglomeris from Korea (Diplopoda: Glomerida: Glomeridae) + + + +Author + +Mikhaljova, Elena V. + + + +Author + +Lim, Kil-Young + +text + + +Zootaxa + + +2006 + +1224 + + +45 +58 + + + +journal article +10.5281/zenodo.172637 +f8158bf1-bb55-4ec9-aa5f-08a093c9032c +1175­5326 +172637 + + + + + + + +Hyleoglomeris unicolorata +Lim + +, +sp. n. + + + + +Figs 1–6 +. + + + + +Material examined + + + +Holotype + +: +1 male +(ChNU), from Goyang, Gyeonggi­do, +South Korea +, collected +17 May 1991 +by K.­Y. Lim. + +Paratypes + +: +1 male +, +2 females +(ChNU), same locality as for +holotype +, collected +17 May 1991 +by K.­Y. Lim. + + + + +Diagnosis. +Differs from congeners mainly by the monochrome coloration without any pattern, combined with the ovoid syncoxital lobe of the telopods and syncoxital lateral horn crowned with wrinkles and a subapical setoid. + + + + +Etymology + +The specific epithet refers to the monochrome coloration of the body. + + + +Description + + +Male. Length 7.5–8.0 mm, width 4.0– +4.5 mm +. Body coloration in alcohol light tan, without any pattern of spots and stripes. Clypeus light tan. Antennae light tan with distal antennomeres brownish tan. Ocelli tan. Tömösváry’s organ light tan. Venter somewhat lighter than dorsum. Legs light tan. + + +Ocelli convex. +Holotype +with 8+1 ocelli on each side of head. +Paratype +with 7+1 ocelli on right side and 8+1 ocelli on left side of head. Antennomere 6 about 2.1–2.2 times longer than wide. Dorsum smooth. Collum with two transverse striae. Thoracic shield with a narrow hyposchism reaching but not protruding beyond hind tergal contour, with 8 delicate striae, of which only four entirely crossing dorsum ( +Fig. 1 +). Some of the striae with branch. Length of striae varied. As usual, anterior border of the thoracic shield with one stria concealed under caudal margin of collum. Pigidium delicately sinuate medially at caudal margin. + + +Leg pair 17 ( +Fig. 2 +) with high, regularly rounded, outer coxal lobes, telopodite 4–jointed. Leg pair 18 ( +Fig. 3 +) with a lancet­shaped syncoxital notch, telopodite 4­jointed, basal segment with sparsely papillate laterally. + + +Telopods ( +Fig. 4 +) massive; central lobe of syncoxite rather large, ovoid, microsetose, with a low and smooth prominence frontally and a shagreen shallow cavity caudally. Syncoxital lateral horns high, slender, setose, directed caudad, each crowned with wrinkles and a subapical setoid ( +Fig. 5 +). Both prefemur and femur micropapillate laterally and mesally. Prefemur with a long, inner, setose finger crowned with a long flagelloid. Femur with a similar but shorter, antero­mesal, setose finger also crowned by a flagelloid and posteriorly with a large inner outgrowth apically bearing a membranous sack curved forward. Caudomedial outgrowth of femur relatively narrow at base ( +Fig. 6 +). Tibia with a long anteromedial seta, with a curved dentiform medial outgrowth posteriorly. + +Caudomedial outgrowth of tibia with a weakly micropapillate tubercle at base. Tarsus with a somewhat curved caudad distal part and a strong subapical seta. + +Female. Length 9.5–10.0 mm, width 5.0– +5.5 mm +. Ocelli 7+1 to 8+1. Antennomere 6 about 2.2–2.3 times longer than wide. Pigidium very slightly sinuate medially at caudal margin. One +paratype +with hyposchism somewhat protruding beyond hind tergal contour. + + + + \ No newline at end of file diff --git a/data/38/4B/97/384B975C15EA7471C15415D9B5BA6BB7.xml b/data/38/4B/97/384B975C15EA7471C15415D9B5BA6BB7.xml new file mode 100644 index 00000000000..e450fc4a8c4 --- /dev/null +++ b/data/38/4B/97/384B975C15EA7471C15415D9B5BA6BB7.xml @@ -0,0 +1,76 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Murex rana +[ +spec. nov. +] + + + +M. testa suturis subvaricosis oppositis compressis scabra, cingulis muricatis, apertura edentula ovata. + +Bonan. recr. +3. +t. +182. + + +Petiv. gaz. t. +100. +f. +12. + + +Rumph. mus. t. +24. +f. G. + + +Gvalt. test. t. +49. +f. L. + + +Argenv. conch. t. +12. +f. P. R. + + +Kratzenst. Regenf. +26. +t. +6. +f. +64. + + + + \ No newline at end of file diff --git a/data/38/4B/C1/384BC198011055FEB90B9156BB004067.xml b/data/38/4B/C1/384BC198011055FEB90B9156BB004067.xml new file mode 100644 index 00000000000..0e885e46d44 --- /dev/null +++ b/data/38/4B/C1/384BC198011055FEB90B9156BB004067.xml @@ -0,0 +1,474 @@ + + + +Two new species of the spider genus Loxosceles (Araneae, Sicariidae) from the Ecuadorian Andes + + + +Author + +Duperre, Nadine +https://orcid.org/0000-0003-2195-878X +Museum of Nature Hamburg - Zoology, Leibniz-Institute for the Analysis of Biodiversity Change (LIB), Centre for Taxonomy and Morphology, Martin-Luther-King-Platz 3, 20146 Hamburg, Germany & American Museum of Natural History, New York, NY, USA +n.duperre@leibniz-lib.de + + + +Author + +Harms, Danilo +https://orcid.org/0000-0002-7189-5345 +Museum of Nature Hamburg - Zoology, Leibniz-Institute for the Analysis of Biodiversity Change (LIB), Centre for Taxonomy and Morphology, Martin-Luther-King-Platz 3, 20146 Hamburg, Germany + + + +Author + +Crespo-Perez, Veronica +https://orcid.org/0000-0002-8811-1965 +Laboratorio de Entomologia, Museo de Zoologia QCAZ, Escuela de Ciencias Biologicas, Pontificia Universidad Catolica del Ecuador, Avenida 10 de Octubre 1076, 170143, Quito, Ecuador + + + +Author + +Tapia, Elicio +Museum of Nature Hamburg - Zoology, Leibniz-Institute for the Analysis of Biodiversity Change (LIB), Centre for Taxonomy and Morphology, Martin-Luther-King-Platz 3, 20146 Hamburg, Germany + +text + + +Evolutionary Systematics + + +2024 + +2024-01-10 + + +8 + + +1 + + +1 +14 + + + + +http://dx.doi.org/10.3897/evolsyst.8.107213 + +journal article +http://dx.doi.org/10.3897/evolsyst.8.107213 +2535-0730-1-1 +651A309753FE49F98B755C5D8AF189F1 +4BE9B0A53B4F5F0F8E641BB304D1D704 + + + + + +Loxosceles guayllabamba +Duperre +& Tapia + +sp. nov. + + + + +Figs 1 +, 2 +, 3 +, 9A, B, G +, Map 1 + + + +Type material. + +Male holotype from Ecuador, Pichincha Province, Quito, Lirios de Carcelen ( +-00.083424 +, +-78.456323 +) 2586 m, 17 Nov. 2019, hand collected in holes and under rocks in dry area, E. Tapia, De Rossi Tapia, ECFN 3678 (QCAZ). +Paratypes +: same data as holotype: 1♀, ECFN 2777 (QCAZ); 1♂, ECFN 3677 (QCAZ); 1♀ ECFN 7773 (QCAZ) 2♀, ECFN 7768 7769 (QCAZ); 2♀1♂ ECFN 7764 (AMNH); 3♀ ECFN 7766 7772 (ZMH-A0014267, A0014268, A0014270); 2♂3juv., hand collected in house, E. Tapia, De Rossi Tapia,(ZMH-A0014271); 1♂, hand collected in garage, E. Tapia, De Rossi Tapia, ECFN 3676 (ZMH-A0015445); 1♂ ECFN 7762 (ZMH-A0014269); 1♀1♂ (USNM); 1♀1♂ (MCZ). + + + +Other material examined. + + +Ecuador +: + +Pichincha + +: +Bosque Protector Jerusalem +( +00.000075 +, +-78.355095 +) +7♂ +10♀ +, collected under rocks, dead trees, old tree bark and old +Agave +leaves, +23.XII.2022 +, +E. E. Tapia +(QCAZ, ZMH-A0019764, 19765, USNM); +Quito +, + +Lirios +de Carcelen + +( +-00.083424 +, +-78.456323 +) + +2586 m + +, +17 Nov. 2019 +, +2juv. +, hand collected in holes and under rocks in dry area, +E. Tapia +, +De Rossi Tapia +(ZMH-A0015443, A0015444); +3♂ +2♀ +5juv. +, ECFN +7761 7763 7765 7767 7771 7774 7937 7938 +(DTC). + +Imbabura + +: Pimapiro [ +00°24'20.25"N +, +77°56'20"W +] + +2038 m + +, +5 Jan 2003 +, +1♂ +1♀ +, +R. Cardenas +(QCAZ) + +. + + + +Diagnosis. + +Males most resemble + +L. rufipes + +(Lucas, 1834) and + +L. lutea + +Keyserling, 1877 but are distinguished as such: from + +L. rufipes + +by their shorter, non-sinuous embolus (Fig. +2A, B, D +) while in the latter the embolus is long and sinuous (see +Gertsch and Ennik 1983 +: fig. 335); from + +L. lutea + +by their palpal tibia not thickened in basal third and femur longer (6.5 +x +longer than wide) (Fig. +2A, B +), while palpal tibia thicker in basal third (Fig. +8A, B +; +Gertsch 1967 +: plate 19, fig. 1) and 4.2 +x +longer than wide ( +Gertsch 1967 +: 166). Females most resemble + +L. alicea + +Gertsch, 1967, + +L. lutea + +, and + +L. binfordae + +sp. nov. but are distinguished by their short spermathecae (as long as wide) with wide bases and small pointed outer lobes (Fig. +3A-D, G, H +); while + +L. alicea + +Gertsch, 1967 has spermathecae without outer lobes ( +Gertsch 1967 +: plate 10, fig. 11); + +L. lutea + +has elongated (1.3 +x +longer than wide) and constricted spermathecae (Fig. +7G, H +) and + +L. binfordae + +sp. nov. has shorter (0.6 +x +longer than wide) spermathecae with wide outer lobes (Fig. +6A-D, G, H +). + + + +Description. + +Male +(holotype): Total length: 6.06; carapace length: 2.7; carapace width: 2.28; abdomen length: 3.36. + + + +Cephalothorax +. + +Carapace light yellow-brown, piriform, with darker red-brown pars cephalica dorsally (Fig. +1A +); clypeus 0.22, light brown. Sternum light yellow, longer than wide; labium light yellow, trapezoidal, fused to sternum; endites yellow, white apically; longer than wide (Fig. +1B +). + + + +Figure 1. + +Loxosceles guayllabamba + +sp. nov. Holotype male. +A. +Habitus, dorsal view; +B. +Habitus, ventral view. Paratype female; +C. +Habitus, dorsal view; +D. +Habitus, ventral view. Scale bars: 1.0 mm. + + + + +Figure 2. + +Loxosceles guayllabamba + +sp. nov. Holotype male. +A. +Palp, prolateral view (arrow points to stridulatory pick); +B. +Palp, retrolateral view; +C. +Male palpal tibia, dorsal view; +D. +Male bulb, apical view. Scale bars: 0.5 mm. + + + + +Figure 3. + +Loxosceles guayllabamba + +sp. nov. Female internal genitalia. +A. +Dorsal view, paratype (ECFN 2777); +B. +Dorsal view, paratype (ECFN 7769); +C. +Dorsal view, paratype (ECFN 7776); +D. +Dorsal view, paratype (ECFN 7770); +E. +SEM, dorsal view uterus (ECFN 7768); +F. +SEM, dorsal view bursa copulatrix (ECFN 7768); +G. +SEM, dorsal view spermathecae (ECFN 7768); +H. +SEM, dorsal view left spermathecae (ECFN 7768). + + + + +Chelicerae +. + +Orange-brown; fused basally, with chelated chelicerae laminae; stridulatory organ well developed with ~34 files; fangs orange-brown, paler distally. + + + +Eyes +. + +Six eyes in three diads; PME: 0.12, ALE: 0.14, PLE: 016, PLE-PLE: 0.77 (Fig. +1A +). + + + +Abdomen +. + +Dorsally grayish, elongated oval (Fig. +1A +); ventrally light gray (Fig. +1B +); colulus triangular. + + + +Legs +. + +Light yellow (Fig. +1A, B +). Legs measurements: I 15.18 (4.10/0.73/4.49/4.59/1.27); II 18.32 (4.54/0.76/5.21/-5.27/1.54); III 13.37 (3.78/0.61/3.66/4.02/1.30); IV 15.45 (4.15/0.75/4.28/4.81/1.46). Leg formula: 2413. + + + +Palp +. + +Femora light yellow, long and thin (1.91 length/0.29 width = 6.5 +x +) with stridulatory pick basally (Fig. +2A +); patellae light yellow; tibiae light yellow, (1.07 length /0.56 width = 1.9 +x +) long and thick, almost straight dorsally, thicker mid-ventrally; tarsus dark reddish orange (Fig. +2A, C +). Palp bulb oval, with evenly, tightly curved embolus (Fig. +2B, D +); tip of embolus not twisted (Fig. +9A, B +, arrow). + + +Female +(paratype): Total length: 8.03; carapace length: 3.27; carapace width: 2.7; abdomen length: 4.76. + + + +Cephalothorax +. + +Carapace red-brown, piriform; darker brown along radiation lines and fovea (Fig. +1C +); clypeus 0.26, dark brown. Sternum orange, longer than wide; labium reddish-brown, trapezoidal, fused to sternum; endites reddish-brown, white apically; longer than wide (Fig. +1D +). + + + +Chelicerae +. + +Dark reddish-brown; fused basally, with chelated chelicerae laminae; stridulatory organ well developed with ~29 files; fangs reddish-brown, paler distally. + + + +Eyes +. + +Six eyes in three diads; PME: 0.14, ALE: 0.16, PLE: 016, PLE-PLE: 0.98 (Fig. +1C +). + +Abdomen +. + +Dorsally grayish, elongated oval (Fig. +1C +); ventrally light gray; colulus triangular (Fig. +1D +). + + + +Legs +. + +Orange-brown (Fig. +1C, D +). Legs measurements: I 13.73 (3.68/0.79/4.08/3.88/1.30); II 15.33 (4.42/0.88/4.59/4.03/1.41); III missing; IV 15.11 (4.41/0.87/3.93/4.52/1.38). Leg formula: 241-. + + + +Palp +. + +Femur light orange with basal stridulatory pick; patellae light orange; tibia and tarsus dark reddish brown. + + + +Genitalia +. + +Spermathecae elongated, apically rounded; as long as wide (1 +x +); with small pointed outer lobe (Fig. +3A +, arrow); bases of spermathecae wide (Fig. +3A-D, G, H +). + + + +Etymology. +The specific name is a noun in apposition taken from the region where the species was collected, Guayllabamba parish. + + +Distribution. + +Ecuador, +Imbabura +and Pichincha provinces. + + + +Natural history. + +Specimens were collected between 2038-2586 m in the inter-Andean valley. Most specimens were collected under rocks, debris, in between leaves of dead Agave plants, and a few specimens were collected in a house or in adjacent garage (Fig. +10 +). + + + + \ No newline at end of file diff --git a/data/38/4C/EA/384CEA6A75B19AA359AEACD3188F07DC.xml b/data/38/4C/EA/384CEA6A75B19AA359AEACD3188F07DC.xml new file mode 100644 index 00000000000..7587ef858c8 --- /dev/null +++ b/data/38/4C/EA/384CEA6A75B19AA359AEACD3188F07DC.xml @@ -0,0 +1,56 @@ + + + +Marine Bryozoa of Greece: an annotated checklist + + + +Author + +Gerovasileiou, Vasilis + + + +Author + +Rosso, Antonietta + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +10672 +10672 + + + + +http://dx.doi.org/10.3897/BDJ.4.e10672 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e10672 +1314-2828--10672 + + + + +Alcyonidium cellarioides (Calvet, 1900) + + + +Notes + +Castritsi-Catharios and Kiortis 1984 +, +Castritsi-Catharios and Kiortis 1985 + + + + \ No newline at end of file diff --git a/data/38/4D/23/384D2345883D34773A0D3D2488E02872.xml b/data/38/4D/23/384D2345883D34773A0D3D2488E02872.xml new file mode 100644 index 00000000000..a43ad7c3b74 --- /dev/null +++ b/data/38/4D/23/384D2345883D34773A0D3D2488E02872.xml @@ -0,0 +1,119 @@ + + + +New species of Bidessonotus Regimbart, 1895 with a review of the South American species (Coleoptera, Adephaga, Dytiscidae, Hydroporinae, Bidessini) + + + +Author + +Miller, Kelly B. + +text + + +ZooKeys + + +2016 + +622 + + +95 +127 + + + + +http://dx.doi.org/10.3897/zookeys.622.9155 + +journal article +http://dx.doi.org/10.3897/zookeys.622.9155 +1313-2970-622-95 +E69EDCC45841428493B9AE8D866A8EB4 + + + +Taxon classification Animalia Coleoptera Dytiscidae + + + +Bidessonotus truncatus J. Balfour-Browne, 1947 +Figs 28, 32 + + + + + +Bidessonotus +truncatus + +J. Balfour-Browne, 1947: 440; +Young 1969 +: 2; +1990 +: 376; + +Bistroem +1988 + +: 18; +Nilsson 2016 +: 99. + + + +Diagnosis. + +Specimens of this species are darkly colored with the elytra nearly evenly dark brown. The prosternal process is relatively broad, flat, apically pointed, and weakly or not sulcate. The apical blade of the male median lobe is slender with the distal margin medially with an elongate spinous +"horn" +or process (Fig. 28a,d). The right lateral lobe has the apical segment relatively slender, medially more broadly expanded and as long as the basal segment (Fig. 28b). The left lateral lobe has the apical segment shorter, broadly obliquely concave apically and bilobed (Fig. 28c). + + + +Discussion. +Little has been reported about this species, but specimens were collected from both lentic and slow lotic habitats. + + +Distribution. + +Known from Bolivia, Brazil, Guayana, Paraguay, Peru, Suriname and Trinidad (Fig. 32, +Young 1990 +). Examined specimens include the following: Guyana: Mayuruni Potaro, Takutu Mountains, +6.216°N +, +59.049°W +, 19 Dec 1983, Spangler, Faitoute, Ed W. (4, USNM). Venezuela: Amazonas, Communidad Porvenir, just S of, +5.341°N +, +67.755°W +, 15 Jan 2009, Short & Garcia (33, SEMC); Amazonas, Road between Puerto Ayacucho and Samariapo, +5.341°N +, +67.755°W +, 06 Jan 2006, Short, Andrew E (4, SEMC); Bolivar, Gran Sabana, between Kavanayen and Rt 10, +5.741°N +, +61.515°W +, 01 Aug 2008, Short, Andrew E (6, SEMC); Bolivar, Gran Sabana, N Santa Elena, Rio Guara at Rt 10, +4.622°N +, +61.094°W +, 17 Jul 2010, Short, Arias, Tellez (2, SEMC); Bolivar, Gran Sabana, N Santa Elena, River at Rt 10 crossing, +4.672°N +, +61.068°W +, 15 Jul 2010, Short, Camacho, Tellez (4, MIZA); Guarico, Hato Masaguaral, +8.566°N +, +67.583°W +, 06 Mar 1986, Spangler & Beaujon (8, USNM); Monagas, Morichal Largo & Temblador, small pond between, +9.096°N +, +62.726°W +, 02 Feb 2010, Short, Garcia, Joly (6, SEMC). + + + + \ No newline at end of file diff --git a/data/38/4D/87/384D87CD4131FFD0FF16631998EB3AD5.xml b/data/38/4D/87/384D87CD4131FFD0FF16631998EB3AD5.xml new file mode 100644 index 00000000000..cf154edbcd0 --- /dev/null +++ b/data/38/4D/87/384D87CD4131FFD0FF16631998EB3AD5.xml @@ -0,0 +1,477 @@ + + + +Review of the spoon tarsus subgroup of Hawaiian Drosophila (Drosophilidae: Diptera), with a description of one new species + + + +Author + +Lapoint, Richard T. + + + +Author + +Magnacca, Karl N. + + + +Author + +O’Grady, Patrick M. + +text + + +Zootaxa + + +2009 + +2003 + + +53 +68 + + + +journal article +10.5281/zenodo.185613 +8ccb9b77-9c91-40de-ac9c-27e6389d7eff +1175-5326 +185613 + + + + + + + +Drosophila waddingtoni +Hardy + + + + + +Figure 3 +e + + + + + + +Drosophila disticha + +Hardy, 1965 +: 249 + + +–252 + +Drosophila waddingtoni + +Basden, 1976 +: 185 + + + + + + + +Diagnosis. +Dense setae are present on the posterior surface of the tibia equal to, or longer than, the tibial spur (see +Fig. 2 +b for example). The legs are yellow, except for brown front coxae and femora. The second tarsal segment is the widest of the group, being 1/3 wider than long. The wings are without any noticeable pigmentation (see +Fig. 3 +e). The thorax is dark brown to black, and the abdomen is mostly dark brown with the last tergum yellow, and the preceding tergites marked with yellow laterally. + + + +Types +: MAUI: + +Holotype +ɗ (BPBM 6344) Waikamoi, +1220 m +, +vii.1956 +, DEH. Locality recorded as “Wai +a +kamoi” on +type +label ( +Evenhuis 1982 +). + + + + +Synonym. + +disticha +Hardy 1965 +: 249 + +preoccupied + + + + +Material Examined. HAWAI‘I: +11ɗ have been studied from the +BPBM +from the following localities: 3 ɗ, Keanakolu, +x.1952 +, +DEH +, +CPH +; 3 ɗ, Kīlauea, +xi.1919 +, WMG; 5 ɗ, from Kawaihae Uka, Kohalas, +x.2006 +, KNM, RTL, GMB. 30 ɗ have been deposited in the +UHIM +from the following localities: 7 ɗ, Kīlauea, +viii.1958 +, JWB; 5 ɗ, Upper Ōla‘a Forest, +vii.1953 +, +DEH +; 3 ɗ, Upper Ōla‘a Forest, +viii.1952 +, +DEH +; 4 ɗ, Upper Ōla‘a Forest, +vii.1956 +, +DEH +; 4 ɗ, Kūlani 5200', +vii.1952 +, WCM; 2 ɗ, Keanakolu, +x.1952 +, +DEH +, +CPH +; 5 ɗ, Kīpuka Kī, +vii.1966 +, KYK. The following material is present at +AMNH +: ɗ, Volcanoes National Park, Kīpuka Puaulu, +O127.4 +, +29.vii.2001 +, +PMO +; 65 ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O132.3 +, +AMCC +105705, +2.viIi.2001 +, +PMO +, +CDS +; 40 ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, O140.C, +AMCC +105687, +12.iv.2002 +, +PMO +, +CDS +. The following material is in the Essig Museum of Entomology at +UC +Berkeley: 2 ɗ, Puu Makaala Trailhead, +O257.1 +, O201319, +11.vii.2004 +, +PMO +, MG; ɗ, Volcanoes National Park, Upper Ōla‘a Forest, end of Wright Road, O272.F, O +200624 +; +20.vii.2004 +, +PMO +, MG, +GS +, AC. + + +LANA‘I: +Over 60 ɗ have been deposited in the +UHIM +the following localities: ɗ, Lāna‘ihale, +vi.1953 +, +DEH +; 12 ɗ, Lāna‘ihale 3300', +iii.1965 +, KYK; 46 ɗ, Lāna‘ihale 3000', +vii.1956 +, dEH; 4 ɗ, Lāna‘ihale 3300', +viii.1964 +, HLC. + + + + +MAUI +: Over 180 ɗ have been deposited in the UHIM from the following localities: 2 ɗ, Pu‘u Kukui, +vi.1953 +, DEH; 2 ɗ, Pu‘u Kukui, +iv.1954 +, DEH; ɗ, Haelaau, +xii.1928 +, OHS; ɗ, Kula Pipeline, +vi.1927 +, OHS; 16 ɗ, Kula Pipeline, +vii.1956 +, DEH; ɗ, Waikamoi, +i.1926 +, OHS; 59 ɗ, Waikamoi, +vii.1956 +, RN; 13 ɗ, Waikamoi, +viii.1958 +, DEH; 88 ɗ, Waikamoi, +vii.1964 +, HLC; 2 ɗ, Waikamoi, +vii.1956 +, DEH; ɗ, Waikamoi, +iii.1966 +, WBH. The following material is present at AMNH: 9 ɗ, Upper Waikamoi Forest Reserve, +5500 ft +., +O41.4 +, +6.vii.1998 +, PMO, SLM; 10 ɗ, 2 Ψ, Waikamoi Forest Reserve, Heed Trail, O50.A, +8.iii.1999 +, PMO, EMC, MPK; 3 ɗ, Waikamoi Forest Reserve, Heed Trail, O55.B, +16–18.iii.1999 +, PMO, JBS; ɗ, Makawao Forest Reserve, Pig Hunter’s Trail, +O56.1 +, +18.vii.1999 +, PMO, JBS; 20 ɗ, Waikamoi Forest Reserve, Heed Trail, O71.A, +2.vi.1999 +, PMO; 3 ɗ, Hanaula, +O72.9 +; +15–16.vi.1999 +, PMO, KYK, KTK, YK; 6 ɗ, 2 Ψ, Waikamoi Forest Reserve, Heed Trail, O73.C, +22.vii.1999 +, PMO, EMC, MPK; 2 ɗ, Waikamoi Forest Reserve, Heed Trail, O74.I, +4.ii.2000 +, PMO; 10 ɗ, Makawao Forest Reserve, Pig Hunter’s Trail, +O153.8 +, AMCC105805, +23.iv.2002 +, PMO, DO; 4 ɗ, Waikamoi Forest Reserve, Heed Trail, O154.H, +23.iv.2002 +, PMO, DO. The following material is in the Essig Museum of Entomology at +UC +Berkeley: ɗ, Waikamoi Forest Reserve, Flume stream, +O300.8 +, O201347, +4.viii.2005 +, PMO, GMB, +CH +, JEG; 4 ɗ, Waikamoi Forest Reserve, Heed Trail, O301.A, O201362, +4.viii.2005 +, PMO, GMB, +CH +, JEG; 10 ɗ, Waikamoi Forest Reserve, Heed Trail, +O303.5 +, O201407, +4.viii.2005 +, PMO, GMB, +CH +, JEG; 6 ɗ, Waikamoi Forest Reserve, Carson Trail, +O305.5 +, +6.viii.2005 +, PMO, GMB; 12 ɗ, Waikamoi Forest Reserve, Heed Trail, +O398.1 +, O +200786 +, +31.vii.2007 +; PMO, KNM, RTL, GMB, KRG. + + +MOLOKA‘I: +23 ɗ have been deposited in the BPBM from the following localities: 3 ɗ, Kamakou Preserve, forest near Hanalilolilo Lookout, O376.C, O201865, +19.ii.2007 +, PMO, KNM, RTL, GMB; 13 ɗ Kamakou Preserve, Puu Kolekole, +O377.6 +, O201874, +19.ii.2007 +, PMO, KNM, RTL, GMB, ɗ Kamakou Preserve, makai of Puu Kolekole Cabin, +O378.4 +, 201890,19. +ii.2007 +, PMO, RTL, GMB; ɗ Kamakou Preserve, Tunnel on trail to Puu Kolekole, +O379.1 +, O201894, +19.ii.2007 +, PMO, KNM, RTL, GMB; 11ɗ, Pepe‘opae, +vii.1959 +, DEH; 4 ɗ, Maunawainui Valley, +vii.1952 +, DEH. Over 50 ɗ have been deposited in the UHIM from the following localities: 16 ɗ, Pu‘u Kolekole, +vii.1952 +, DEH, MT; 16 ɗ, Pu‘u Kolekole, +vii.1953 +, DEH, MT; 4 ɗ, Pu‘u Kolekole, +iii.1963 +, DEH; 1ɗ, Pepe‘opae, +vii.1959 +, DEH; 4 ɗ, Maunawainui Valley, +vii.1952 +, DEH. The following material is present at AMNH: 46 ɗ, Kamakou Preserve, Puu Kolekole, +O35.1 +, +1.vii.1998 +, PMO, SLM; 83 ɗ, Kamakou Preserve, Puu Kolekole, +O58.5 +, +19–21.iii.1999 +, PMO, JBS; 37 ɗ, Kamakou Preserve, Puu Kolekole, O101.C, +26–27.vii.1999 +, PMO, EMC, MPK; 26 ɗ, 55 Ψ, Kamakou Preserve, Puu Kolekole, +O146.2 +, AMCC105707, +15–16.iv.2002 +, PMO, CDS, DO; 1ɗ, 13 Ψ, Kamakou Preserve, Pepeopae Boardwalk Trail, +O150.2 +, AMCC105755, +16.iv.2002 +, PMO, CDS, DO; 2 ɗ, 7f, Kamakou Preserve, forest near Hanalilolilo Lookout, O151.C, AMCC105765, +17.iv.2002 +, PMO, CDS, DO. The following material is in the Essig Museum of Entomology at +UC +Berkeley: 35 ɗ, Kamakou Preserve, Puu Kolekole, +3854 ft +., +O283.1 +, O201705, +28–29.vii.2004 +, PMO, CDS. + + + + +Distribution. +This species is endemic to Maui Nui and the Big Island of Hawai‘i. + + +Behavior. +Speith (1966: 273); +Grossfield (1968) +; +Kambysellis and Heed (1971) +. + + + + +Chromosomes. +The metaphase complement of this species is 5 rods and 1 dot ( +Clayton 1969 +; +Yoon & Richardson 1978 +). + + +Ecology. +Nutritional requirements ( +Robertson et al 1968 +); This species has been reared from leaves of + +Cheirodendron trigynum +(Araliaceae) + +from Hawai‘i, Maui, Moloka‘i and Lana‘i; leaves of + +Tetraplasandra + +sp ( +Araliaceae +) from Hawai‘i; leaves and stems of + +Clermontia + +sp ( +Campanulaceae +) from Hawai‘i and Lana‘i; leaves of + +Myrsine lessertiana +(Myrsinaceae) + +from Moloka‘i; leaves of + +Pittosporum + +sp ( +Pittosporaceae +) from Moloka‘i ( +Heed 1968 +; +Magnacca et al 2008 +; +Mangan 1978 +). + + +Illustrations. +Morphological structures of this species are depicted in multiple publications including: egg ( +Kambysellis and Heed 1971: 34, fig. 2.3; 36, figs. 4.1, 4.2 +); foreleg ( +Hardy 1965: 250, fig. 82a +); ovary ( +Kambysellis and Heed 1971: 35, fig. 3.1 +); phallus ( +Kaneshiro 1976: 267, fig. 5e +); terminalia, female, lateral ( +Hardy 1965: 250, fig. 82b +); terminalia, male, lateral ( +Hardy 1965: 250, fig. 82c +); +Takada 1966 +: 318, fig. 1.8). + + +Molecular Biology. +DNA sequences ( +Kambysellis & Craddock 1997 +; +O’Grady & DeSalle 2008 +; +O’Grady & Zilversmit 2004 +). + + + + +Discussion. + +Drosophila waddingtoni + +has the widest range of any spoon tarsus group species and is found throughout Hawai‘i and Maui Nui. Several individuals from Maui have been collected that grade in coloration of the tibia from yellow (normal) to dark brown. + + + + \ No newline at end of file diff --git a/data/38/4D/87/384D87CD4131FFD2FF1665C2991C3C91.xml b/data/38/4D/87/384D87CD4131FFD2FF1665C2991C3C91.xml new file mode 100644 index 00000000000..ce7bf38bce7 --- /dev/null +++ b/data/38/4D/87/384D87CD4131FFD2FF1665C2991C3C91.xml @@ -0,0 +1,252 @@ + + + +Review of the spoon tarsus subgroup of Hawaiian Drosophila (Drosophilidae: Diptera), with a description of one new species + + + +Author + +Lapoint, Richard T. + + + +Author + +Magnacca, Karl N. + + + +Author + +O’Grady, Patrick M. + +text + + +Zootaxa + + +2009 + +2003 + + +53 +68 + + + +journal article +10.5281/zenodo.185613 +8ccb9b77-9c91-40de-ac9c-27e6389d7eff +1175-5326 +185613 + + + + + + + +Drosophila sordidapex +Grimshaw + + + + + +Figure 3 +b + + + + + + +Drosophila sordidapex + +Grimshaw, 1901 +: 63 + + + + + + + +Diagnosis. +The palpi and mouthparts are light brown. The thorax is yellow to light brown and the legs are completely yellow. The wing posseses a distinct marking that completely darkens the apical half of cell R2+3, the posterior apical margin of cell R1 and anterior apical margin of cell R4+5. Unlike other species, this spot is much darker and is not diffuse, with defined margins (see +Fig. 3 +b), although in some specimens (including the +holotype +), it may be distinctly following the veins with a small clear area in the middle of cell R2+3. The abdomen is dark brown to black dorsally with yellow sides except for the completely yellow last tergite. + + + +Types +. HAWAI‘I: + +Holotype +ɗ (BMNH) Ōla‘a Forest, +vii. 1895 +. [probably collected by R. C. L. Perkins]. + + + + +Material Examined. HAWAI‘I: +11 ɗ have been deposited in the +BPBM +from the following localities: ɗ, Stainback Highway, Tom's Trail, 3200', +x.2006 +, KNM, RTL, GMB; 4 ɗ, Kahuku, Pu‘u Akihi Gulch, +i.2006 +, KNM; ɗ, +HAVO +escape road, 3900’, +vi.2006 +, KNM; ɗ, Hionamoa Stream, Ka‘ū Forest, +x.2006 +, KNM, RTL, GMB; ɗ, Ōla‘a Forest, +x.2006 +, KNM, RTL, GMB; ɗ, Kukuiopa‘e, South Kona Forest Reserve, +x.2006 +, KNM, RTL, GMB; 2 ɗ, Laupāhoehoe, 3700', +x.2006 +, KNM, RTL, GMB. Over 50 ɗ have been deposited in the +UHIM +from the following localities: 23 ɗ, Keanakolu, +x.1952 +, +DEH +; 13 ɗ, Upper Ōla‘a Forest, +viii.1952 +, +DEH +; 5 ɗ, Upper Ōla‘a Forest, +viii.1953 +, +DEH +; 5 ɗ, Upper Ōla‘a Forest, +vii.1963 +, WBH; 3 ɗ, Upper Ōla‘a Forest, +vii.1964 +, LHT; 7 ɗ, Upper Ōla‘a Forest, +vii.1956 +DEH +; 4 ɗ, Pu‘u Hualalai, +vi.1966 +, WBH; 3 ɗ, Kaiholeua, Kohala Mountains, +viii.1952 +, +DEH +; ɗ, Forest above Pa‘auilo, +vii.1953 +, +DEH +; ɗ, Keauhou Ranch, Kīlauea, +vii.1953 +, +DEH +; ɗ, Honaunau Forest, +vii.1966 +KYK. The following material is present at +AMNH +: ɗ, Neuneu Road, Kaloko Mauka, North Kona, +O38.6 +, +3.vii.1998 +, +PMO +, SLM; 5 ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O117.4 +, +23.ii.2001 +, +PMO +; 2 ɗ, Volcanoes National Park, Ōla‘a Forest, transect 16, +O120.2 +, +25.ii.2001 +, +PMO +, DF; ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O132.8 +, +AMCC +105696, +2.viIi.2001 +, +PMO +, +CDS +; 5 ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O140.8 +, +AMCC +105684, +12.iv.2002 +, +PMO +, +CDS +. The following material is in the Essig Museum of Entomology at +UC +Berkeley: ɗ, Volcanoes National Park, Ōla‘a Forest, near pole 48, O247.H; O201459; +6–7.vii.2004 +, +PMO +, MG, +CDS +. + + + + +Distribution. +This species is endemic to the Big Island of Hawai‘i. + + +Behavior: +Speith (1966: 274). + + + + +Ecology. +This species has been reared from leaves of + +Cheirodendron trigynum +(Araliaceae) + +; leaves of + +Ilex anomala +(Aquifoliaceae) + +( +Heed 1968 +). + + +Illustrations. +Morphological structures of this species are depicted in multiple publications including: foreleg ( +Hardy 1965: 470, fig. 190a +); phallus ( +Kaneshiro 1976: 267, fig. 5b +); terminalia, male, lateral ( +Hardy 1965: 470, fig. 190c +); wing ( +Hardy 1965: 470, fig. 190b +). + + + + \ No newline at end of file diff --git a/data/38/4D/87/384D87CD4134FFD4FF16631F9AC63D49.xml b/data/38/4D/87/384D87CD4134FFD4FF16631F9AC63D49.xml new file mode 100644 index 00000000000..af8f145076e --- /dev/null +++ b/data/38/4D/87/384D87CD4134FFD4FF16631F9AC63D49.xml @@ -0,0 +1,252 @@ + + + +Review of the spoon tarsus subgroup of Hawaiian Drosophila (Drosophilidae: Diptera), with a description of one new species + + + +Author + +Lapoint, Richard T. + + + +Author + +Magnacca, Karl N. + + + +Author + +O’Grady, Patrick M. + +text + + +Zootaxa + + +2009 + +2003 + + +53 +68 + + + +journal article +10.5281/zenodo.185613 +8ccb9b77-9c91-40de-ac9c-27e6389d7eff +1175-5326 +185613 + + + + + + + +Drosophila neutralis +Hardy + + + + + + + + + +Drosophila neutralis + +Hardy, 1965 +: 383 + + +–385 + + + + + +Diagnosis. +The labella, palpi and frons are all brown. Dense setae on the posterior portion of the tibia of the fore legs of the males are prone, not erect, and never longer than the tibial spur (see +Fig. 2 +c for example). Legs are completely yellow, except for the last tarsal segments which are brown. The apical portion of the wings are hyaline (see +Fig. 3 +e for example). Abdomen is mostly dark brown, except for the last two tergites and the sides of first tergite which are yellow. + + + +Types +. HAWAI‘I: + +Holotype +ɗ (BPBM 6409) Kīlauea, +viii.1958 +, JWB ( +Evenhuis 1982 +). + + + + +Material Examined. HAWAI‘I: +32 ɗ have been studied in the +BPBM +from the following localities: 3 ɗ, +29 mi +. Ōla‘a, +viii.1925 +, WMG; ɗ, Stainback Highway, 3600’, +x.2006 +, KNM, RTL, GMB; 2 ɗ, Stainback Highway, Tom's Trail, 3200’, +x.2006 +, KNM, RTL, GMB; 5 ɗ, Hionamoa Stream, Ka‘ū Forest, +x.2006 +, KNM, RTL, GMB; 3 ɗ, Ōla‘a Forest, +x.2006 +, KNM, RTL, GMB; 2 ɗ, Ōla‘a Forest, Tr 18, +ii.2007 +, KNM; 4 ɗ, Ōla‘a Forest, Tr +18 vi.2006 +, KNM; 4 ɗ, +HAVO +escape road, 3900’, +vi.2006 +, KNM; ɗ, +HAVO +Kīpuka Puaulu, 4000’, +vi.2006 +, KNM; ɗ, Pu‘u Huluhulu, +x.2006 +, KNM, RTL, GMB; ɗ, Kukuiopa‘e, South Kona, +x.2006 +, KNM, RTL, GMB; 5 ɗ, Laupāhoehoe, 3700', +x.2006 +, KNM, RTL, GMB. Over 50 ɗ have been deposited in the +UHIM +from the following localities: 20 ɗ, Upper Ōla‘a Forest, +viii.1952 +, +DEH +; 6 ɗ, Upper Ōla‘a Forest, +vii.1953 +, +DEH +; 8 ɗ, Upper Ōla‘a Forest, +vii.1956 +, +DEH +; ɗ, Nāpau Crater, Kīlauea, +vii.1952 +, +DEH +; ɗ, Pauahi 4300', Kīlauea, +vii.1952 +, +DEH +; 10 ɗ, Kīlauea, +viii.1958 +, JWB; 6 ɗ, Fern Forest, Upper Ōla‘a Forest, +iii.1966 +, KYK; 2 ɗ, Kīlauea, +viii.1966 +, KYK. The following material is present at +AMNH +: ɗ, Forest behind Volcano Solid Waste Transfer Station, +O40.2 +, +5.vii.1998 +, +PMO +, SLM; 2 ɗ, Forest behind Volcano Solid Waste Transfer Station, +O51.4 +, +12–14.iii.1999 +, +PMO +, JBS; ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O128.5 +, +29.vii.2001 +, +PMO +, +CDS +. The following material is in the Essig Museum of Entomology at +UC +Berkeley: ɗ, Tree Planting Road, +O256.8 +; O201316; +11.vii.2004 +, +PMO +, MG; ɗ, Kohala Mountains, Top of Waipio Falls, +O269.6 +, O +200623 +, +16.vii.2004 +, +PMO +, +CDS +, +GS +, +SH +, MG. + + + + +Distribution. +This species is endemic to the Big Island of Hawai‘i. + + +Ecology. +This species has been reared from the bark of + +Tetraplasandra oahuensis +(Araliaceae) + +; the leaves and bark of + +Cheirodendron trigynum +(Araliaceae) + +( +Heed 1968 +; +Magnacca et al 2008 +; +Mangan 1978 +). + + + + +Illustrations. +Morphological structures of this species are depicted in multiple publications including: foreleg ( +Hardy 1965: 384, fig. 148b +); phallus ( +Kaneshiro 1976: 267, fig. 5h +); terminalia, male, lateral ( +Hardy 1965: 384, fig. 148c +). + + +Chromosomes. +The metaphase complement of this species is 5 rods and 1 dot ( +Yoon & Richardson 1978 +). + + + + \ No newline at end of file diff --git a/data/38/4D/87/384D87CD4134FFD7FF1667DB989D3C92.xml b/data/38/4D/87/384D87CD4134FFD7FF1667DB989D3C92.xml new file mode 100644 index 00000000000..e0f1acc7451 --- /dev/null +++ b/data/38/4D/87/384D87CD4134FFD7FF1667DB989D3C92.xml @@ -0,0 +1,188 @@ + + + +Review of the spoon tarsus subgroup of Hawaiian Drosophila (Drosophilidae: Diptera), with a description of one new species + + + +Author + +Lapoint, Richard T. + + + +Author + +Magnacca, Karl N. + + + +Author + +O’Grady, Patrick M. + +text + + +Zootaxa + + +2009 + +2003 + + +53 +68 + + + +journal article +10.5281/zenodo.185613 +8ccb9b77-9c91-40de-ac9c-27e6389d7eff +1175-5326 +185613 + + + + + + + +Drosophila mimiconformis +Hardy + + + + + + + + + +Drosophila mimiconfromis + +Hardy, 1965 +: 367 + + +–369 + + + + + +Diagnosis. +The labella, palpi and frons are all yellow. The fore-tibia of the males lacks numerous vertical setae present on other species (see +Fig. 2 +c). The wings are completely hyaline (see +Fig. 3 +e). The thorax ranges in color from light to dark brown. The legs are entirely yellow. The abdomen is completely black. + + + +Types +. MOLOKA‘I: + +Holotype +ɗ (BPBM 6401) Maunawainui Valley, +vii.1952 +, DEH ( +Evenhuis 1982 +). + + + + +Material Examined. MOLOKA‘I: +2 ɗ has been studied from +BPBM +: ɗ, Maunawainui Valley, +vii.1952 +, +DEH +; ɗ, East Kawela Gulch, +ii.2007 +, KNM. 26 ɗ have been deposited in the +UHIM +from the following localities: ɗ, Hanalilolilo, +viii.1953 +, MT; 15 ɗ, Maunawainui Valley, +vii.1952 +, +DEH +; 2 ɗ, Pu‘u Ali‘i, +vii.1953 +, +DEH +, MT; 4 ɗ, Pu‘u Kolekole, +v.1965 +, +DEH +; 3 ɗ, Pu‘u Kolekole, +vi.1964 +, +DEH +; 2 ɗ, South of Hanalilolilo, +vii.1964 +, +DEH +. + + + + +Distribution. +This species is endemic to Maui Nui (Moloka‘i, Maui, Lana‘i). + + +Ecology. +This species has been reared from leaves of + +Cheirodendron trigynum +(Araliaceae) + +on Maui and Moloka‘i; leaves of + +Tetraplasandra + +sp ( +Araliaceae +) on Moloka‘i; leaves of + +Ilex anomala + +on Maui ( +Aquifoliaceae +) ( +Heed 1968 +). + + + + +Illustrations. +Morphological structures of this species are depicted in multiple publications including: foreleg ( +Hardy 1965: 368, fig. 140a +); phallus ( +Kaneshiro 1976: 267, fig. 5a +); terminalia, male, lateral ( +Hardy 1965: 368, fig. 140b +). + + + + +Discussion. + +D. mimiconformis + +is the only species endemic to the island of Moloka‘i. It is very similar to + +D. conformis + +of the island of Hawai‘i, but can be easily distinguished by location of collection and a lack of pigmentation in the apical portion of the wing. + + + + \ No newline at end of file diff --git a/data/38/4D/87/384D87CD4135FFD6FF1665C29BFA3AE4.xml b/data/38/4D/87/384D87CD4135FFD6FF1665C29BFA3AE4.xml new file mode 100644 index 00000000000..15c1c1506ed --- /dev/null +++ b/data/38/4D/87/384D87CD4135FFD6FF1665C29BFA3AE4.xml @@ -0,0 +1,174 @@ + + + +Review of the spoon tarsus subgroup of Hawaiian Drosophila (Drosophilidae: Diptera), with a description of one new species + + + +Author + +Lapoint, Richard T. + + + +Author + +Magnacca, Karl N. + + + +Author + +O’Grady, Patrick M. + +text + + +Zootaxa + + +2009 + +2003 + + +53 +68 + + + +journal article +10.5281/zenodo.185613 +8ccb9b77-9c91-40de-ac9c-27e6389d7eff +1175-5326 +185613 + + + + + + + +Drosophila incognita +Hardy + + + + + +Figure 2 +d + + + + + + +Drosophila incognita + +Hardy, 1965 +: 319 + + +–320 + + + + + +Diagnosis. +The anterioapical portion of the forebasistarus of males have 6 to 8 long setae (see +Fig. 2 +d). The thorax is dark brown. The apical wing spot is similar to that of + +D. conformis + +but darker (see +Fig. 3 +c for example). The lateral portion of most of the abdomen and the entire final tergite is yellow. + + + +Types +. HAWAI‘I: + +Holotype +ɗ (BPBM 6377) Upper Ōla‘a Forest, +viii.1952 +, DEH ( +Evenhuis 1982 +). + + + + +Material Examined. HAWAI‘I: +ɗ has been studied from the +BPBM +: Ōla‘a Trail 18, +vi.2006 +, KNM. 6 ɗ have been studied from the +UHIM +: 2 ɗ, Upper Ōla‘a Forest, +vii.1956 +, +DEH +; ɗ, Kīlauea, +viii.1958 +, JWB; 2 ɗ, Upper Ōla‘a Forest, +viii.1952 +, +DEH +; ɗ, Kaiholena, Kohala Mountains, +viii.1952 +, +DEH +. The following material is present at +AMNH +: ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O132.7 +, +AMCC +105701, +2.viIi.2001 +, +PMO +, +CDS +. The following material is in the Essig Museum of Entomology at +UC +Berkeley: ɗ, Tree Planting Road, +O256.8 +; O201315; +11.vii.2004 +, +PMO +, MG. + + +Illustrations. +Morphological structures of this species are depicted in multiple publications including: forleg ( +Hardy 1965: 320, fig. 118a +); phallus ( +Kaneshiro 1976: 267, fig. 5c +); terminalia, male, lateral ( +Hardy 1965: 320, fig. 118c +); wing ( +Hardy 1965: 320, fig. 118c +) + + + + +Discussion. +This species is morphologically very close to + +D. conformis + +and the defining features are the long setae on the basitarsus. + + + + \ No newline at end of file diff --git a/data/38/4D/87/384D87CD4135FFD7FF16668A9B3A3B56.xml b/data/38/4D/87/384D87CD4135FFD7FF16668A9B3A3B56.xml new file mode 100644 index 00000000000..1fe36f31893 --- /dev/null +++ b/data/38/4D/87/384D87CD4135FFD7FF16668A9B3A3B56.xml @@ -0,0 +1,171 @@ + + + +Review of the spoon tarsus subgroup of Hawaiian Drosophila (Drosophilidae: Diptera), with a description of one new species + + + +Author + +Lapoint, Richard T. + + + +Author + +Magnacca, Karl N. + + + +Author + +O’Grady, Patrick M. + +text + + +Zootaxa + + +2009 + +2003 + + +53 +68 + + + +journal article +10.5281/zenodo.185613 +8ccb9b77-9c91-40de-ac9c-27e6389d7eff +1175-5326 +185613 + + + + + + + +Drosophila kikalaeleele, +Lapoint, Magnacca & O’Grady + +new species + + + + + + +Diagnosis +: This species is very similar to + +D. sordidapex + +in overall morphology, notably the discrete marking at the apical portion of the wing, and is inferred to be the sister species. + +Drosophila kikalaeleele + +is differentiated by the last two tergites being completely yellow on an otherwise completely brown to black abdomen, and by having the anal plate black. + + + + +Male Description. +Body length: +2.5 to 3 mm +. Wing length: +3 mm +. +Head +. Lower portion of frons yellow. Ocellar triangle black. Vertex ranges from brown to black. Face ranges from light to dark brown. Gena yellow. Ocellar and vertical setae ~ as long as antennal arista. Anterior reclinate slightly shorter than proclinate. Clypeus, labella and palpi yellow. Several weak black setae on apical portion of palpi. Labellum fringed with weak yellow setae. Mouthparts not ornate. First and second antennal segments yellow. Third antennal segment completely dark brown to black. 6 dorsal rays, 2 ventral rays and apical fork on arista. + + +Thorax +. Thorax dorsally light brown with four rufous stripes running anterior to posterior. Scutellum entirely yellow. The anepisternum dark brown, otherwise lateral portion of thorax yellow tinged with light brown. Posterior dorsocentral setae 1/3 longer than anterior dorsocentral setae. Apical scutellar setae ~2/3 as long as the basal scutellar setae. Haltere completely yellow. + + +Legs. +Basitarsi lack setae apically; second tarsal segment concave and 1/3 longer than third tarsal segment. Fore and mid legs entirely yellow except for slight darkening of fifth tarsal segment and middle tibia. Mid leg yellow except for brown tibia. Short setae ½ as long as preapical bristle on tibia. + + +Wings +. Discretely edged wing spot darkens apical half of cell R2+3, lower apical margin of cell R1 and upper apical margin of cell R4+5. Remainder of wing hyaline. Costal fringe extends halfway between apical margin of cell R2+3 (see +Fig. 3 +b). + + +Abdomen +. Dorsal tergites dark brown to black with yellow on posterior margins of each tergite, except for yellow to light brown fifth and sixth tergites. Sternites yellow. Anal plate dark black. Genitalia identical to + +D. sordidapex + +. + + + + + +Type +Material. + +Holotype +ɗ ( +BPBM +16909), South Kona Forest Reserve, +x.2006 +, RTL, KNM, GMB. + + +Material Examined. HAWAI‘I: +2 ɗ have been deposited into the +BPBM +: ɗ, Ōla‘a Trail 18, +vi.2006 +, KNM; ɗ South Kona Forest Reserve, +x.2006 +, RTL, KNM, GMB. 30 ɗ have been deposited in the +UHIM +from the following localities: 19 ɗ, Hualālai, +vii.1970 +, WBH, MD, TL; 3 ɗ, Hualālai, 3400’, +xii.1969 +, KYK; ɗ, Kīpuka No 9, Saddle Rd, +vi.1969 +, WBH; 4 ɗ, Kīpuka No 14, 5100’, Saddle Road, +vii.1969 +, WBH; ɗ, Pu‘u Huluhulu, +vii.1969 +, RHR; ɗ, Greenwell Ranch, Pauahi, +vi.1974 +; ɗ, Upper Ōla‘a Forest Reserve, +x.1988 +, KYK. + + + + +Distribution and Ecology. +Reared from +Ilex +leaves by W. B. Heed. Collected at Hualālai, Pu‘u Huluhulu, the Saddle Road Kīpukas and the Ōla‘a Forest. + + + + +Etymology +: A combination of the Hawaiian words ‘ele‘ele = black and kikala = buttock, posterior. + + +Relationships. +Based on overall morphology, especially wing patterning, this species is close to + +D. sordidapex + +. + + + + \ No newline at end of file diff --git a/data/38/4D/87/384D87CD4137FFD5FF1661D09F763F81.xml b/data/38/4D/87/384D87CD4137FFD5FF1661D09F763F81.xml new file mode 100644 index 00000000000..55c0b76f9a0 --- /dev/null +++ b/data/38/4D/87/384D87CD4137FFD5FF1661D09F763F81.xml @@ -0,0 +1,486 @@ + + + +Review of the spoon tarsus subgroup of Hawaiian Drosophila (Drosophilidae: Diptera), with a description of one new species + + + +Author + +Lapoint, Richard T. + + + +Author + +Magnacca, Karl N. + + + +Author + +O’Grady, Patrick M. + +text + + +Zootaxa + + +2009 + +2003 + + +53 +68 + + + +journal article +10.5281/zenodo.185613 +8ccb9b77-9c91-40de-ac9c-27e6389d7eff +1175-5326 +185613 + + + + + + + +Drosophila percnosoma +Hardy + + + + + +Figure 2 +e + + + + + + +Drosophila percnosoma + +Hardy, 1965 +: 410 + + +–412 + + + + + +Drosophila septuosa + +Hardy, 1965 +:410 + + +–412, +syn. nov +. + + + + + +Diagnosis. +A large (~ +4 mm +) species. The mouthparts and palpi are dark brown to black, along with the other features of the head. Tibia densely setose on posterior surface without setae longer than the tibial spur (see +Fig. 2 +e). Femora are dark brown while the rest of the leg is yellow. The thorax is a dark brown to black. The wings are subhyaline with a faint infuscation of brown at the apical portion of the wing (see +Fig. 3 +e). The abdomen is dark brown to black. + + + +Types +. HAWAI‘I: + +Holotype +ɗ (BPBM 6419) Upper Ōla‘a Forest, +viii.1958 +, DEH. Allotype Ψ (BPBM 6419a) same collection as +holotype +( +Evenhuis 1982 +). + + + + + + +D. septuosa + +Type +: + +Holotype +ɗ (BPBM 6443) Kīlauea, +viii.1958 +, JWB ( +Evenhuis 1982 +). + + + + +Material Examined. HAWAI‘I: +27 ɗ have been studied from the +BPBM +from the following localities: ɗ, Glenwood, +iii.1919 +, OHS; 1 ɗ +29 mi +Ōla‘a, +viii.1925 +, WMG; 3 ɗ, Stainback Highway, Tom's Trail, 3200', +x.2006 +, KNM, RTL, GMB; 5 ɗ, Hionamoa Stream, Ka‘ū Forest, +x.2006 +, KNM, RTL, GMB; ɗ, Kīpuka 9, Kaūmana Trail, +x.2006 +, KNM, RTL, GMB; 4 ɗ, Ōla‘a Forest, +x.2006 +, KNM, RTL, GMB; 4 ɗ, from Pu‘u Huluhulu, +x.2006 +, KNM, RTL, GMB; 5 ɗ, Laupāhoehoe, 3700', +x.2006 +, KNM, RTL, GMB; 3 ɗ, Ōla‘a Forest, Tr +18 ii.2006 +, KNM. Over 70 ɗ have been deposited in the +UHIM +from the following localities: 4 ɗ, Upper Ōla‘a Forest, +viii.1952 +, WCM; 15 ɗ, Kīlauea, +viii.1958 +, JWB; 24 ɗ, Upper Ōla‘a Forest, +viii.1952 +, +DEH +, WCM; 3 ɗ, Kahuku Ranch, +vii.1953 +, +DEH +; ɗ, Upper Ōla‘a Forest, +vii.1953 +, +DEH +, WCM; 2 ɗ, Upper Ōla‘a Forest, +viii.1956 +, +DEH +; ɗ, Keauhou Ranch, Kīlauea, +viii.1953 +, +DEH +; ɗ, Pauahi 4300', Kīlauea, +vii.1952 +, +DEH +; 7 ɗ, Lower Ōla‘a Forest, +vii.1964 +, LHT; 2 ɗ, Upper Ōla‘a Forest, +vii.1964 +, LHT; 4 ɗ, Upper Ōla‘a Forest, +ix.1964 +, HTS; 4 ɗ, Upper Ōla‘a Forest, +vi.1966 +, WBH; 2 ɗ, Upper Ōla‘a Forest, +vii.1963 +, WBH; 3 ɗ, Nāpau Crater, Kīlauea, +vii.1956 +, +DEH +; ɗ, Upper Ōla‘a Forest, +vii.1956 +, +DEH +. The following material is present at +AMNH +: 8 ɗ, Forest behind Volcano Solid Waste Transfer Station, +O40.3 +, +5.vii.1998 +, +PMO +, SLM; 10 ɗ, Stainback Highway, +7–8.ii.1999 +, +O49.1 +, +PMO +, SLM; 6 ɗ, Forest behind Volcano Solid Waste Transfer Station, +O51.1 +, +12–14.iii.1999 +, +PMO +, JBS; 5 ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O93.5 +, +7.ix.2000 +, +PMO +; 2 ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O112.3 +, +20.x.2000 +, +PMO +; 3 ɗ, Volcanoes National Park, Kīpuka Puaulu, +O127.3 +, +29.vii.2001 +, +PMO +; 2 ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O128.3 +, +29.vii.2001 +, +PMO +, +CDS +; 44 ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O132.4 +, +AMCC +105700, +2.viIi.2001 +, +PMO +, +CDS +; 49 ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O140.8 +, +AMCC +105685, +12.iv.2002 +, +PMO +, +CDS +. The following material is in the Essig Museum of Entomology at +UC +Berkeley: 12 ɗ, Volcanoes National Park, Ōla‘a Forest, near pole 48, +O247.2 +; O201444; +6–7.vii.2004 +, +PMO +, MG, +CDS +; 4 ɗ, Tree Planting Road, +O256.8 +; O201317; +11.vii.2004 +, +PMO +, MG; 3 ɗ, Puu Makaala Trailhead, +O257.1 +, O201500, +11.vii.2004 +, +PMO +, MG; 2 ɗ, Volcanoes National Park, Upper Ōla‘a Forest, end of Wright Road, O272.F, O +200640 +; +20.vii.2004 +, +PMO +, MG, +GS +, AC; 24 ɗ, Volcanoes National Park, Ōla‘a Forest, near pole 44, +O307.6 +, O +201114 +; +8.viii.2005 +; +PMO +, GMB, +CH +, JEG. + + +Maui +: 10 ɗ have been studied from +UHIM +from Waikamoi Forest, +v.1966 +, WBH. + + + + +Distribution. +This species is endemic to the Big Island of Hawai‘i. + + +Behavior. +Bell and Kipp (1994) +. + + + + +Chromosomes. +The metaphase complement of this species is 5 rods and 1 dot ( +Clayton 1968 +). + + +Ecology. +This species has been reared from leaves of + +Cheirodendron trigynum + +and + +Tetraplasandra oahuensis +(Araliaceae) + +; leaves of + +Clermontia + +sp ( +Campanulaceae +) ( +Heed 1968 +; +Magnacca et al 2008 +; +Mangan 1978 +). + + +Illustrations. +Morphological structures of this species are depicted in multiple publications including: foreleg ( +Hardy 1965 +: 411, figs. 163a, b); terminalia, male, lateral ( +Hardy 1965: 411, fig. 163c +) + + +as +septuosa + +: + +foreleg ( +Hardy 1965: 462, fig. 187d +); phallus ( + +Kaneshiro 1976: 267, fig. +5g + +); terminalia, male, lateral ( +Hardy 1965: 462, fig. 187c +). + + +Chromosomes. +The metaphase complement of this species is 5 rods and 1 dot ( +Yoon & Richardson 1978 +). + + +Molecular Biology. +DNA sequences ( +O’Grady & DeSalle 2008 +). + + + + +Discussion. +Based on our morphological analysis, + +Drosophila septuosa +( +Hardy 1965 +) + +is synonymous with + +Drosophila percnosoma +( +Hardy 1965 +) + +. The descriptions of both species by Hardy are very similar, with only minor differences between species, all well within normal variation for the group. We have examined both +holotypes +in the BPBM as well as the above series and compared both to the description found that all the characters used by Hardy to describe each species describe both +holotypes +and their respective series. On closer inspection the minor character differences Hardy utilizes in his descriptions are not present in one of the two +holotypes +. + +Drosophila percnosoma + +is chosen because of its page priority in the original description and greater usage in the literature: 7 for + +D. percnosoma + +( +Bell & Kipp 1994 +; +Clayton 1968 +; +Hardy 1965 +; +Heed 1968 +; +Magnacca et al 2008 +; +Mangan 1978 +; +O’Grady & DeSalle 2008 +) and 5 for + +D. septuosa + +( +Hardy 1965 +; +Heed 1968 +; +Kaneshiro 1976 +; +Magnacca et al 2008 +; +Yoon & Richardson 1978 +). We have identified 10 individuals from UHIM that were reared from + +Pittosporum + +leaves by W. B. Heed in 1966 from Waikamoi Forest on Maui, but this is the only instance of + +D. percnosoma + +being found off of the island of Hawai‘i. + + + + \ No newline at end of file diff --git a/data/38/4D/87/384D87CD4138FFD8FF16632499873D1A.xml b/data/38/4D/87/384D87CD4138FFD8FF16632499873D1A.xml new file mode 100644 index 00000000000..7a81d5d1b6c --- /dev/null +++ b/data/38/4D/87/384D87CD4138FFD8FF16632499873D1A.xml @@ -0,0 +1,278 @@ + + + +Review of the spoon tarsus subgroup of Hawaiian Drosophila (Drosophilidae: Diptera), with a description of one new species + + + +Author + +Lapoint, Richard T. + + + +Author + +Magnacca, Karl N. + + + +Author + +O’Grady, Patrick M. + +text + + +Zootaxa + + +2009 + +2003 + + +53 +68 + + + +journal article +10.5281/zenodo.185613 +8ccb9b77-9c91-40de-ac9c-27e6389d7eff +1175-5326 +185613 + + + + + + + +Drosophila dasycnemia +Hardy + + + + + +Figures 2 +b and 3d + + + + + + +Drosophila dasycnemia + +Hardy, 1965 +: 236 + + +–238 + + + + + +Diagnosis. +Elongate setae present on the posterior surface of fore tibia. The legs are yellow except for brown coxae and terminal portions of the last tarsi (see +Fig. 2 +b). Wings are lightly infuscated with a brown marking apically, which extends from cell R1 to halfway through cell R4+5 (see +Fig. 3 +d). The thorax is brown, and the abdomen is almost entirely dark brown, with the last tergite being yellow. + + + +Types +. HAWAI‘I: + +Holotype +ɗ (BPBM 6337) Upper Ōla‘a Forest, +viii.1952 +, DEH ( +Evenhuis 1982 +). + + + + +Material Examined. HAWAI‘I: +61ɗ have been deposited in the +BPBM +: ɗ, Kaiwiki, +ix.1918 +, OHS; 2 ɗ, Stainback Highway, 3600’, +x.2006 +, KNM, RTL, GMB; 2 ɗ, Stainback Highway, Tom's Trail, 3200', +x.2006 +, KNM, RTL, GMB; 2 ɗ, Kīpuka 9, Kaūmana Trail, +x.2006 +, KNM, RTL, GMB; 5 ɗ, Ōla‘a Forest, +x.2006 +, KNM, RTL, GMB; 5 ɗ, Ōla‘a Tr 18, +vi.2006 +, KNM; 10 ɗ, Ōla‘a Tr 18, +ii.2006 +, KNM; 3 ɗ, Kawaihae Uka, Kohalas, +x.2006 +, KNM, RTL, GMB; ɗ, Kukuiopa‘e, South Kona Forest Reserve, +x.2006 +, KNM, RTL, GMB; 5 ɗ, Laupāhoehoe, 3700', +x.2006 +, KNM, RTL, GMB. 30 ɗ from the +UHIM +have been examined from the following localities: 5 ɗ, Upper Ōla‘a, +vii.1956 +, +DEH +, WCM; 3 ɗ, Upper Ōla‘a, +viii.1958 +, +DEH +, WCM; 12 ɗ, Upper Ōla‘a, +viii.1952 +, +DEH +, WCM; 7 ɗ, Kīlauea, +viii.1958 +, JWB; 2 ɗ, Volcano, +v.1915 +, AB; ɗ, Mud Lane, +vi.1964 +, +DEH +, LHT. The following material is present at +AMNH +: 5 ɗ, Forest behind Volcano Solid Waste Transfer Station, +O40.4 +, +5.vii.1998 +, +PMO +, SLM; 14 ɗ, Stainback Highway, +7–8.ii.1999 +, +O49.3 +, +PMO +, SLM; 2 ɗ, Forest behind Volcano Solid Waste Transfer Station, +O51.5 +, +12–14.iii.1999 +, +PMO +, JBS; 5 ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O93.6 +, +7.ix.2000 +, +PMO +; 16 ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O132.6 +, +2.viIi.2001 +, +PMO +, +CDS +. The following material is in the Essig Museum of Entomology at +UC +Berkeley: 8 ɗ, Volcanoes National Park, Ōla‘a Forest, near pole 48, +O247.2 +; O201321; +6–7.vii.2004 +, +PMO +, MG, +CDS +; 5 ɗ, Tree Planting Road, +O256.8 +; O201497; +11.vii.2004 +, +PMO +, MG; 4 ɗ, Puu Makaala Trailhead, +O257.1 +, O201318, +11.vii.2004 +, +PMO +, MG; ɗ, Kohala Mountains, Top of Waipio Falls, +O269.6 +, O201595, +16.vii.2004 +, +PMO +, +CDS +, +GS +, +SH +, MG; 2 ɗ, Volcanoes National Park, Upper Ōla‘a Forest, end of Wright Road, O272.F, O +200625 +; +20.vii.2004 +, +PMO +, MG, +GS +, AC. + + + + +Distribution. +This species is endemic to the island of Hawai‘i. + + +Behavior. +Speith (1966:272). + + + + +Ecology. +This species has been reared from leaves of + +Cheirodendron trigynum +(Araliaceae) + +( +Heed 1968 +; +Mangan 1978 +). + + +Illustrations. +Morphological structures of this species are depicted in multiple publications including: foreleg ( +Hardy 1965: 237, fig. 74a +); phallus ( +Kaneshiro 1976: 267, fig. 5 Ψ +); terminalia, male, lateral ( +Hardy 1965: 237, fig. 74c +); wing ( +Hardy 1965 +: 237, fig. 74b; +Edwards et al 2007 +: fig7). + + +Molecular Biology. +DNA sequences ( + +Baker +& DeSalle 1997 + +). + + + + \ No newline at end of file diff --git a/data/38/4D/87/384D87CD4138FFDBFF1661449EBA3F75.xml b/data/38/4D/87/384D87CD4138FFDBFF1661449EBA3F75.xml new file mode 100644 index 00000000000..5ae64cb6683 --- /dev/null +++ b/data/38/4D/87/384D87CD4138FFDBFF1661449EBA3F75.xml @@ -0,0 +1,132 @@ + + + +Review of the spoon tarsus subgroup of Hawaiian Drosophila (Drosophilidae: Diptera), with a description of one new species + + + +Author + +Lapoint, Richard T. + + + +Author + +Magnacca, Karl N. + + + +Author + +O’Grady, Patrick M. + +text + + +Zootaxa + + +2009 + +2003 + + +53 +68 + + + +journal article +10.5281/zenodo.185613 +8ccb9b77-9c91-40de-ac9c-27e6389d7eff +1175-5326 +185613 + + + + + + + +Drosophila contorta +Hardy + + + + + + + + + +Drosophila contorta + +Hardy, 1965 +: 226 + + +–227 + + + + + +Diagnosis. +Elongate setae present on the posterior surface of fore tibia. The front basitarsus of the males is curved and the face is distinctly concave. The spoon is as long as the third tarsal segments, nearly as wide and distinctly concave. The coloration of the species is very light. The wings are subhyaline (see +Fig. 3 +e for example). + + + +Types +. MAUI: + +Holotype +ɗ (BPBM 6333) Waikamoi, +1220 m +, +vii.1956 +, DEH. Locality recorded as “Wai +a +kamoi” on +type +label ( +Evenhuis 1982 +). + + + + + +Material Examined. +MAUI +: + +The following material is present at +AMNH +: ɗ, Makawao Forest Reserve, Pig Hunter’s Trail, O153.K, +AMCC +105817, +23.iv.2002 +, +PMO +, DO. + + + + +Distribution. +This species is endemic to Maui. + + +Illustrations. +Foreleg ( +Hardy 1965: 227, fig. 69b +); head ( +Hardy 1965 +: 227, fig. 69a. + + + + \ No newline at end of file diff --git a/data/38/4D/87/384D87CD413BFFD8FF1661879B6C3EA2.xml b/data/38/4D/87/384D87CD413BFFD8FF1661879B6C3EA2.xml new file mode 100644 index 00000000000..f0557754ab9 --- /dev/null +++ b/data/38/4D/87/384D87CD413BFFD8FF1661879B6C3EA2.xml @@ -0,0 +1,152 @@ + + + +Review of the spoon tarsus subgroup of Hawaiian Drosophila (Drosophilidae: Diptera), with a description of one new species + + + +Author + +Lapoint, Richard T. + + + +Author + +Magnacca, Karl N. + + + +Author + +O’Grady, Patrick M. + +text + + +Zootaxa + + +2009 + +2003 + + +53 +68 + + + +journal article +10.5281/zenodo.185613 +8ccb9b77-9c91-40de-ac9c-27e6389d7eff +1175-5326 +185613 + + + + + + + +Drosophila fastigata +Hardy + + + + + + + + + +Drosophila fastigata + +Hardy, 1965 +: 271 + + +–273 + + + + + +Diagnosis. +Legs entirely yellow. Apex of the basitarsus extends dorsally into a hatchet shaped lobe with two setae. The second tarsal segment is as long as wide and not concave. Wings hyaline, lacking distinct markings (see +Fig. 3 +e for example). Thorax brown tinged with yellow, darker dorsally. Scutellum ranges from dark brown to black. Abdominal tergites are brown, except for last tergite which is yellow. + + + +Types +. O‘ AHU: + +Holotype +ɗ (BPBM 6529) Pūpūkea, +vii.1958 +, DEH ( +Evenhuis 1982 +). + + + + +Material Examined. O‘AHU: +9 ɗ have been studied from the +BPBM +: ɗ, Poamoho Trail, 1700’, +v.1953 +, +DEH +; ɗ, Mt. Ka‘ala, +iv.1929 +, EHB; 2 ɗ, Manoa Cliff Trail Trail, +ii.2007 +, KNM; 5 ɗ, Mt. Ka‘ala, 3950’, +v.2007 +, KNM. + + + + +Distribution. +This species is endemic to the island of O‘ahu. + + +Ecology. +This species has been reared from leaves of + +Cheirodendron platyphyllum +(Araliaceae) + +( +Heed 1968 +). + + + + +Illustrations. +Foreleg ( +Hardy 1965: 272, fig. 93a +); terminalia, male, lateral ( +Hardy 1965 +: 272, figs. 93b, c). + + + + +Discussion. + +D. fastigata + +is the only spoon tarsus species endemic to O‘ahu. Due to its morphological similarity to + +D. atroscutellata + +, this species is included in this group, but is also considered basal due to the reduced spoon. + + + + \ No newline at end of file diff --git a/data/38/4D/87/384D87CD413EFFDBFF16638D99E03AD5.xml b/data/38/4D/87/384D87CD413EFFDBFF16638D99E03AD5.xml new file mode 100644 index 00000000000..ec3d94e7449 --- /dev/null +++ b/data/38/4D/87/384D87CD413EFFDBFF16638D99E03AD5.xml @@ -0,0 +1,280 @@ + + + +Review of the spoon tarsus subgroup of Hawaiian Drosophila (Drosophilidae: Diptera), with a description of one new species + + + +Author + +Lapoint, Richard T. + + + +Author + +Magnacca, Karl N. + + + +Author + +O’Grady, Patrick M. + +text + + +Zootaxa + + +2009 + +2003 + + +53 +68 + + + +journal article +10.5281/zenodo.185613 +8ccb9b77-9c91-40de-ac9c-27e6389d7eff +1175-5326 +185613 + + + + + + + +Drosophila conformis +Hardy + + + + + +Figures 2 +c and 3c + + + + + + +Drosophila conformis + +Hardy, 1965 +: 319 + + +–320 + + + + + +Diagnosis. +Tibia lacking profuse setae equal to, or longer than, the tibial spur. Legs are completely yellow, except for last tarsal segment being brown (see +Fig. 2 +c). The thorax ranges from light to dark brown. The wings have a diffuse brown marking apically, which extends from cell R1 to halfway through cell R4+5 (see +Fig. 3 +c). The abdomen is completely black. + + + +Types +. HAWAI‘I: + +Holotype +ɗ (BPBM 6330) Upper Ōla‘a Forest, +vii.1953 +, DEH. Allotype Ψ (BPBM 6330a) same collection as +holotype +( +Evenhuis 1982 +). + + + + +FIGURE 2. +Fore-legs of selected males a) + +D. atroscutellata + +, b) + +D. dasycnemia + +, c) + +D. conformis + +, d) + +D. incognita + +, and e) + +D. percnosoma + +. + + + + +Material Examined. HAWAI‘I: +16ɗ have been studied from the +BPBM +: 4 ɗ, Kīlauea, +viii.1958 +, JWB; ɗ, Kīlauea Field Station, +3900 ft +., +vi.2006 +, KNM; ɗ, Manukā +vii.2006 +, KNM; ɗ, Stainback Highway, Tom's Trail, 3200', +x.2006 +, KNM, RTL, GMB; 2 ɗ, Pu‘u Huluhulu, +x.2006 +, KNM, RTL, GMB; 2 ɗ, Laupāhoehoe, 3800', +x.2006 +, KNM, RTL, GMB; 5 ɗ, Ōla‘a, Tr 18, +ii.2006 +, KNM. 22 ɗ deposited in the +UHIM +have been examined from the following localities: 3 ɗ, Kīlauea, +viii.1958 +, JWB; 9 ɗ, Upper Ōla‘a, +viii.1952 +, +DEH +; ɗ, Nāpau Crater, Kīlauea, +vii.1953 +, +DEH +; ɗ, Nāpau Crater, Kīlauea, +vii.1953 +, +DEH +; 6 ɗ, Keanakolu, +vi.1966 +, WBH; 2 ɗ, Hōnaunau Forest Reserve, +ii.1966 +, WBH. The following material is present at +AMNH +: ɗ, Stainback Highway, +7–8.ii.1999 +, +O49.2 +, +PMO +, SLM; 2 ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O112.2 +, +20.x.2000 +, +PMO +; ɗ, Volcanoes National Park, Kīpuka Puaulu, +O127.5 +, +29.vii.2001 +, +PMO +; 2 ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O128.4 +, +29.vii.2001 +, +PMO +, +CDS +; 18 ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O132.5 +, +AMCC +105703, +2.viiI.2001 +, +PMO +, +CDS +; 48 ɗ, Volcanoes National Park, Ōla‘a Forest, near +Pole +44, +O140.7 +, +AMCC +105686, +12.iv.2002 +, +PMO +, +CDS +. The following material is in the Essig Museum of Entomology at +UC +Berkeley: 3 ɗ, Volcanoes National Park, Ōla‘a Forest, near pole 48, +O247.2 +; O201320; +6–7.vii.2004 +, +PMO +, MG, +CDS +. + + + + +Distribution. +This species is endemic to the Big Island of Hawai‘i. + + +Behavior. +Shelly (1987 +; +1990 +). + + + + +Ecology. +This species has been reared from leaves of + +Ilex anomala +(Aquifoliaceae) + +( +Heed 1968 +). + + +Illustrations. +Morphological structures of this species are depicted in multiple publications including: foreleg ( +Hardy 1965 +: 220, figs. 66a, b); phallus ( +Kaneshiro 1976: 267, fig. 5d +); terminalia, male, lateral ( +Hardy 1965: 220, fig. 66c +). + + +Molecular Biology. +DNA sequences ( +O’Grady & DeSalle 2008 +). + + + + \ No newline at end of file diff --git a/data/38/4D/87/384D87CD413EFFDDFF16675F9E513F1C.xml b/data/38/4D/87/384D87CD413EFFDDFF16675F9E513F1C.xml new file mode 100644 index 00000000000..67759d1b9b1 --- /dev/null +++ b/data/38/4D/87/384D87CD413EFFDDFF16675F9E513F1C.xml @@ -0,0 +1,202 @@ + + + +Review of the spoon tarsus subgroup of Hawaiian Drosophila (Drosophilidae: Diptera), with a description of one new species + + + +Author + +Lapoint, Richard T. + + + +Author + +Magnacca, Karl N. + + + +Author + +O’Grady, Patrick M. + +text + + +Zootaxa + + +2009 + +2003 + + +53 +68 + + + +journal article +10.5281/zenodo.185613 +8ccb9b77-9c91-40de-ac9c-27e6389d7eff +1175-5326 +185613 + + + + + + + +Drosophila atroscutellata +Hardy + + + + + +Figures 2 +a and 3a + + + + + + +Drosophila atroscutellata + +Hardy, 1966 +: 200 + + + + + + + +Diagnosis. +The spoon structure of + +Drosophila atroscutellata + +males is highly reduced relative to the other taxa in this subgroup. The forebasitarsi is slightly extended apically and densely setose with 7 bristles that start at the apex and extend 2/3 of the length of the segment. The second tarsal segment on the forelegs of the male is barely wider than the third tarsal segment, about as long and lacking concavity. Legs mostly yellow, with a dark brown margin at the apical end of the middle tibia (see +Fig. 2 +a). Thorax light yellow except for the dark brown scutellum. The wings are hyaline except for a dark apical spot extending from the anterior portion of vein R2+3 to halfway through cell M1 (see +Fig. 3 +a). + + + +Types +. KAUA‘I: + +Holotype +ɗ (BPBM 11258), Halemanu Valley, +1220m +, +28.viii.1964 +, HTS. Allotype Ψ (BPBM 11258a), same collection as +holotype +. +Type +locality reported as “Malemanu Valley” by +Evenhuis (1982) +. + + + + +Material Examined. KAUA‘I: +8 ɗ have been studied from the +BPBM +: ɗ, Kōke‘e, +3600 ft +, +vii.1963 +, HLC, FEC & MRW; 2 ɗ, Kōke‘e, +3600 ft +., +vi.1964 +, HLC, FEC & MRW; 2 ɗ, Halemanu Valley, +4000 ft +, +vi.1964 +, FEC, MRW, +DEH +& HTS; 3 ɗ, Nu‘alolo Trail, +3800 ft +., +v.2007 +, KNM. Over 40 ɗ and 25 Ψ in the +UHIM +were also examined from the following localities: 4 ɗ and 4 Ψ, from Kōke‘e, 3600', +iii.1964 +, MRW; ɗ, Kōke‘e, 3600', +iv.1964 +, +DEH +; 15 ɗ, Kōke‘e, 3600', +vi. 1964 +, +DEH +, HTS, HLC; ɗ and 2 Ψ, Kōke‘e, 3600', +vi.1966 +, +DEH +; 4 ɗ, Halemanu Valley, 4000', +iii.1964 +, MRW; 16 ɗ and 14 Ψ, Halemanu Valley, 4000', +vi.1964 +, +DEH +, HTS, HLC; 3 ɗ and 5 Ψ, Halemanu Valley, 4000', +viii.1964 +, +DEH +, HTS. + + + + +Distribution. +This species is endemic to wet forest habitat on Kaua‘i. + + +Chromosomes. +The metaphase complement of this species is 5 rods and 1 dot ( +Clayton 1968 +; +Yoon & Richardson 1978 +). + + + + +Illustrations. +Foreleg ( +Hardy 1966 +: 201, figs. 3c, d); mouthparts ( +Hardy 1966: 201, fig. 3a +); wing ( +Hardy 1966: 201, fig. 3b +); middle tibia ( +Hardy 1966: 201, fig. 3e +); male genitalia, ventral and lateral ( +Hardy 1966 +: 201, figs. 3f, g); female genitalia, lateral ( +Hardy 1966: 201, fig. 3h +). + + + + +Discussion. + +Drosophila atroscutellata + +is the only spoon tarsus species recorded from Kaua‘i. It is considered the most basal member of the group because of its highly reduced spoon. + + + + \ No newline at end of file diff --git a/data/38/4D/8B/384D8BA9BD0F5160AD5D92C039B6407E.xml b/data/38/4D/8B/384D8BA9BD0F5160AD5D92C039B6407E.xml new file mode 100644 index 00000000000..ea063d57d35 --- /dev/null +++ b/data/38/4D/8B/384D8BA9BD0F5160AD5D92C039B6407E.xml @@ -0,0 +1,903 @@ + + + +Bembidion (Ocydromus) terryerwini sp. nov. from Iran (Coleoptera, Carabidae, Bembidiina) + + + +Author + +Neri, Paolo +Via Guido Rossa 21 " San Lorenzo ", 47121, Forli (FC), Italy + + + +Author + +Toledano, Luca +Museo Civico di Storia Naturale di Verona, Lungadige Porta Vittoria 9, 37129, Verona, Italy +lucatole2@libero.it + +text + + +ZooKeys + + +2021 + +2021-06-16 + + +1044 + + +221 +228 + + + + +http://dx.doi.org/10.3897/zookeys.1044.63607 + +journal article +http://dx.doi.org/10.3897/zookeys.1044.63607 +1313-2970-1044-221 +9322962E47664CC6AB93E461B423FED8 +0128E2D5593D551A945F074EA4774CF5 + + + + +Bembidion (Ocydromus) terryerwini +sp. nov. +Figures 2 +, 3 +, 6 +, 7 + + + +Material examined. + + + +Holotype + +, +1 ♂ +, " +N 29°21'14.7" +E 57°20'31.7" +/ +Iran +, Prov. +Kerman +, + +Rayen + +, +Goroah +, / +Babtahoune +, + +Bachufer +- +Schotterbank + +/ +06.06.2014 + +2700 m + +/ leg. +Schnitter +" (CTVR). +We +added the following label (red, printed) to the specimen: " +Bembidion (Ocydromus) terryerwini +Neri & Toledano, 2021 - +Holotypus +" + +. + + +Paratypes + +: +24 ♂♂ +12 ♀♀ +, same collecting data as the holotype (CTVR, JM, PN, PS) + +; + +4 ♂♂ +3 ♀♀ +, " +N 29°23'35.4" +E 57°25'44.4 +Iran +, / +Prov. +Kerman +, +Rayen +, +Anbaroutak +, / +Bachufer +/ +Schotterbank +/ +06.06.2014 + +2350m + +/ leg.: +Schnitter +" (PN, PS) + +; + +22 ♂♂ +24 ♀♀ +, " +N 30°31'18.4" +E 57°09'44.6" +/ Iran, Prov. +Kerman, Kerman +N / Darb-e-Asiab, waterfall near / +Kuhpayeh +, + +Schlucht + +- +Schotterbank +/ +07.06.2014 + +2600 m + +/ leg. +Schnitter +" (CTVR, PN, PS) + +; + +7 ♂♂ +5 ♀♀ +, " +N 29°32'49.6" +E 57°17'56.5" +/ +Iran +, +Prov +, +Kerman +, +Rayen +/ waterfall near +Kuh-e Hazar +/ + +Bachufer +- +Schotterbank + +/ +05.06.2014 + +2920 m + +/ leg. +Schnitter +" (CTVR, PS) + +; + +1 ♂ +1 ♀ +, " +Iran +, +Prov. +Kerman +, +Kuh-e +/ +Lalehzar +, + +3400-3600 m + +/ +04.06.2014 +, 29°27'52" N / 56°45'65" E / leg. +A. Weigel +" (CTVR) + +; + +1 ♂ +, " +Iran +( +Kerman prov. +) / +Kūh-e + +Lalehzar + +vill. ca + +3000-3600 m + +/ +N 29°28'41" +E 56°48'21" +/ (river valley, river bank, / in gravel) / +4.VI.2014 +Wrase & Laser" (CTVR) + +; + +2 ♂♂ +3 ♀♀ +, " +Kerman prov. +15 Km E / +Korin +, +Kub-e-Lalehzar Mts. +/ ( + +3000 m + +) / +18-5-2008 +Iran / +A. Anichtchenko +leg." (CTVR, MT) + +; + +5 ♂♂ +8 ♀♀ +, " +Iran +( +Kerman Prov. +) / waterfall at +Darb-e-Asiab +vill. / N +Kerman + +2600m + +/ +N 30°31'18.4" +/ +E 57°09'44.6" +/ (canyon, in gravel/under stones) / +7.VI.2014 +D. Wrase +" (CTVR, DW, PN) + +; + +2 ♂♂ +2 ♀♀ +, " +Iran +( +Kerman Prov. +) / waterfall at +Darb-e-Asiab +vill. / N +Kerman + +2600m + +/ +N 30°31'18.4" +/ +E 57°09'44.6" +/ (canyon, in gravel/under stones) / +2.VI.2014 +B. Laser +" (DW) + +; + +2 ♂♂ +2 ♀♀ +, " +IRAN +( +Kerman Prov. +) / waterfall at +Darb-e-Asiab +vill. / nr. +Kuhpayeh +vill. N +Kerman +/ ca + +2500 m + +/ +N 30°31'18.4" +/ +E 57°09'44.6" +/ (canyon, in gravel/under stones) / +2.06.2014 +D. Wrase +" (DW) + +; + +3 ♂♂ +3 ♀♀ +, " +Iran +( +Kerman Prov. +) / +Kuh-e Lalehzar +/ N Lalehzar vill. ca. + +3000-3600 m + +/ +N 29°28'41" +/ +E 56°48'21" +/ (river valley, river bank, / in gravel / +4.VI.2014 +Wrase & Laser" (CTVR, DW) + +; + +1 ♂ +, " +Iran +( +Kerman Prov. +) / +Kuh-e Hezar + +2920 m + +/ high plain above +Abshar-e +/ +Rayen +water fall (SW Rayen) / +N 29°32'49.6" +/ +E57°17'56.5" +/ (brook bank, in gravel / sifted, from detritus) / +5.VI.2014 +Wrase" (DW) + +; + +20 ♂♂ +31 ♀♀ +, " +Iran +( +Kerman Prov. +/ +Rayen distr. +) +Goruh Village +/ +Babtahoune + +2700 m + +/ +N 29°21'14.7" +/ +E57°20'31.7" +/ (river bank, in gravel / partly with vegetation) / +6.VI.2014 +Wrase & Laser" (CTVR, DW, PN) + +; + +1 ♀ +, " +Iran +( +Kerman prov. +) / +Anbaroutak +vill. nr. + +Rayen + +/ + +2350 m + +/ +N 29°23'54.4" +E 57°25'44.4" +/ (brook bank, in gravel-under / stones, partly overgrown) / +6.VI.2014 +Wrase & Laser" (DW) + +; + +1 ♂ +, "IR +Kerman +/ +Rusk +/ +19-4-2008 +/ +Muilwijk +leg." (CTVR) + +; + +22 ♂♂ +29 ♀♀ +, " +Iran +, +Maimand +, prov. +Kerman +, +160 km +W +Kerman +, +8.5.2010 +Orszulik +lgt." (CTVR, KO, KR, PN); +1 ♂ +2 ♀♀ +, " +Iran +, prov +Kerman +, +Sarbizhan +, +140 km +S +Kerman +, +4.5.2010 +, +Orszulik +lgt." (KO, KR); +1 ♀ +, "IR +Kerman +Darmazar Kuh-e Bahr Aseman +22.iii.2007 +leg. +J. Muilwijk +" (JM); +1 ♂ +2 ♀♀ +, "IR +Kerman +Darmazar Kuh-e Bahr Aseman +21.iv.2008 +leg. +J. Muilwijk +" (JM); +3 ♂♂ +1 ♀ +, "IR +Kerman +Rabor env. +22.iii.2007 +leg. +J. Muilwijk +" (JM); +1 ♀ +, "IR +Kerman + +30 km +North Baft + +20.iii.2007 +leg. +J. Muilwijk +" (JM); +1 ♀ +, "IR +Kerman +Kuh-e Hezar +21.iv.2008 +leg. +J. Muilwijk +" (JM) + +; + +8 ♂♂ +10 ♀♀ +, " +Iran +7.5.1999 +/ Sir +Kūh +, +Yazd +env. / lgt. Orszulik" (CTVR, KO, KR, PN) + +; + +3 ♂♂ +3 ♀♀ +, "Iran C +7.5.1999 +/ +Yazd +env. / +Mt. Sir +Kūh +/ +L. Klima +leg." (CTVR, JM, KR) + +; + +1 ♂ +, " +Iran +, +Yazd +, +Shir +Kūh +/ 5 Km S Taft / +23.5.2008 + +1600-1700 m + +/ leg. + +Muehle +" + +(CTVR) + +; + +4 ♂♂ +5 ♀♀ +, "IR +Yazd +/ M Sir Kou / +14-4-2008 +/ +Muilwijk +leg. 2008" (DW, JM). +We +added to the specimens the following label (red, printed): " +Bembidion (Ocydromus) terryerwini +Neri & Toledano, 2021 - +Paratypus +" + +. + + + +Type locality. + +Iran, Prov. Kerman, +Rayen +, Goroah, Babtahoune 2700 m, 29°21'14.7"N, 57°20'31.7"E. + + + +Comparative material. + +We were able to compare the species herein described with abundant material from several collections (CTVR, PN, DW, PS, JM), except for +ispartanum nairicum +Iablokoff-Khnzorian, 1976 and +sokolowskyi +Fassati, 1957 that were compared based on the literature, by original descriptions or other publications. Of +sokolowskyi +, Werner Marggi kindly provided a photo of the +holotype +taken in the Coll. Fassati. We also examined the following type material: +1 ♂ +, +paratype +of +B. semilotum +Netolitzky, 1911 "Sultanabad / Th. Strauss [printed] // +semilotum +[handwritten] / det. Netolitzky [printed] // CO / TYPUS [red, printed]" (CTVR), +2 ♀♀ +. +paratypes +of +B. hiekei +Mueller-Motzfeld +, 1986 "Turkm., Kopet Dag / Salzquelle 2 Km v. / Tschuli b.Firjusa / 18.9.76, leg. F. Hieke [printed] // +PARATYPUS +[red, handwritten] // +Bembidion +[printed] / +hiekei +n.sp. [handwritten] // det. +Mueller +1985 [printed]" (PN). + + + +Diagnosis. + +A +Bembidion +of the subgenus +Bembidion Ocydromus +and member of the + +Bembidion decorum + +group; very similar to + +B. hiekei + +Mueller-Motzfeld +, 1986, but recognizable from the latter by a less transverse pronotum with narrow lateral gutter and punctured anterior transverse impression and adjacent area. + + + +Figures 1-7. +1 +habitus of +Bembidion (Ocydromus) hiekei +Mueller-Motzfeld +, paratype, (PN), 5.90 mm +2 +habitus of +B. (O.) terryerwini +sp. nov., holotype (CTVR), 5.20 mm +3 +spermatheca of +B. (O.) terryerwini +sp. nov., paratype (PN) +4 +habitus of +B. (O.) sokolowskyi +Fassati, holotype, (MHNG), 5 mm +5 +pronotum of +Bembidion (Ocydromus) hiekei +Mueller-Motzfeld +, paratype, (PN) +6 +pronotum of +B. (O.) terryerwini +Neri & Toledano, sp. nov., holotype (CTVR) +7 +median lobe of the aedeagus of +B. (O.) terryerwini +sp. nov., holotype (CTVR), 1.02 mm. + + + + +Description of holotype + + +(Fig. +2 +). + +Total body length 5.20 mm. +Coloration +: head and pronotum black, with green metallic reflections, elytra brown, scutellar area blackish brown and sutural interval brown at the internal side. Antennae yellow-orange, only slightly darkened from the apical half of antennomere 4. Palps yellow-orange. Legs yellow-orange with femora with faint brown reflections. + + +Head +: maximum width, including eyes, 1.07 mm; interocular distance 0.62 mm; smooth, punctured in the median portion of the frons at the posterior half of the eye; microsculpture present in the posterior portion of the neck. Eyes markedly protruding, temples very short, almost absent. Wide frontal furrows, with a few punctures. Antennae long 2.68 mm. + + +Pronotum +(Fig. +6 +): length along the mid line 1.03 mm; width of the anterior margin 0.87 mm, maximum width 1.26 mm, width of base 0.93 mm; pronotal width/pronotal length ratio 1.22; slightly transverse; posterior margin slightly convex at middle, oblique towards the hind angles; anterior margin rectilinear with angles evidently bent ventrally; sides entirely rebordered, narrowing evidently and markedly sinuate towards base with which they form a large right angle, despite of the oblique sides of the base; lateral gutter narrow, of homogeneous width; basal foveae subquadrate, with scattered punctures and long laterobasal carina; median line sharp; anterior transverse impression and neighboring area with numerous (about 20) very sharp punctures; basal transverse impression rugose-punctate. Microsculpture in short, polygonal transverse sculpticells, barely visible on disc. + + +Elytra +: length 3.20 mm, maximum overall width, slightly beyond the middle, 2.00 mm; overall shape slightly ovoid with evident shoulders; completely microsculptured with sharp transverse polygonal sculpticells; intervals flat; striae and punctation evident but superficial, visible also near the apex but disappearing at apex. Macropterous species. + + + +Male genitalia. +Medium-small sized (1.02 mm), with ventral margin only slightly concave and apical fourth bent ventrally; endophallus almost completely included in the median lobe; extremely elongated apex. + + +Intraspecific variability. + +The paratypes generally match with the holotype in color and morphology. The brown color of the elytra may be more or less intense, from reddish to dark brown; the palps may be slightly darkened at apex. The pronotum may be slightly more transverse. The microsculpture of the pronotal disc may be more or less visible; the fine punctation at the anterior transverse pronotal impression, always present and sharp, may show a variable number of punctures. The ♂♂ are long from 4.70 to 5.70 mm and the ♀♀ from 4.80 to 5.70 mm. The length of aedeagus (Fig. +7 +) ranges from 1.00 to 1.13 mm, the reservoir of the spermatheca (Fig. +3 +) is 0.23 mm long. + + + +Derivatio nominis. + +This beautiful species is named in memory of the late Terry Erwin (1940-2020), excellent, very kind, collaborative, and friendly man, and excellent globally acknowledged entomologist, who contributed to the taxonomic research of the tribe +Bembidiini +through numerous publications (e.g., +Erwin 1971 +, +1972 +, +1973 +, +1974a +, +b +, +1975 +, +1976 +, +1977 +, +1978 +, +1982 +, +1984 +; +Erwin and Kavanaugh 1980 +, +1981 +, +1999 +: +Erwin et al. 2010 +: +Kavanaugh and Erwin 1992 +). + + + +Distribution. +The new species is known from the Kerman and Yazd Provinces, in central Iran. + + +Comparative notes. + +The species of + +Bembidion decorum + +group currently reported from Iran and neighboring regions are eleven. The + +Bembidion decorum + +group includes species with pronotum microsculptured at least at sides and elytra unicolorous greenish, bluish metallic, or brown. Eleven species of this group are currently known from Iran and neighboring regions: +Bembidion (Ocydromus) decorum bodemeyeri +K. Daniel & J. Daniel, 1902 (Bulgaria, Greece, Macedonia, Turkey); +B. (O.) decorum subconvexum +K. Daniel & J. Daniel, 1902 (Azerbaijan, Armenia, Georgia, Russia: South European Territory, Iran, Turkey); +B. (O.) siculum smyrnense +Apfelbeck, 1904 (Albania, Bosnia Herzegovina, Bulgaria, Croatia, Greece, Macedonia, Romania, Turkey, Ukraine, Yugoslavia A: Cyprus, Israel, Lebanon, Syria, Turkey); +B. (O.) siculum durudense +Marggi & Huber, 1999 (Azerbaijan, Armenia, Georgia, Russia: South European Territory, Iran, Turkey); +B. (O.) ispartanum ispartanum +Netolitzky, 1930 (Armenia, Iran, Israel, Turkey); +B. (O.) ispartanum nairicum +Iablokoff-Khnzorian, 1976 (Armenia, Georgia); +B. (O.) zolotarewi +Reitter, 1910 (Armenia, Georgia, Russia: South European Territory, Iran); +B. (O.) semilotum +Netolitzky, 1911 (Armenia, Iran, Turkey); +B. (O.) hiekei +Mueller-Motzfeld +, 1986 (Iran, Turkmenistan); +B. (O.) sokolowskyi +Fassati, 1957 (Afghanistan); +B. (O.) hasurada pagmanicum +Fassati, 1959 (Afghanistan). Their aedeagi, except for + +Bembidion sokolowskyi + +, are well documented by + +Mueller-Motzfeld +(1986) + +. + +Bembidion terryerwini + +is distinguishable from the above-mentioned species, excluding + +Bembidion hiekei + +, by the brown elytral color; from + +Bembidion hiekei + +(Figs +1 +and +5 +) by the less transverse pronotum with narrow lateral gutter and the anterior transverse impression and neighboring area with several punctures; from + +Bembidion hasurada +Bembidion pagmanicum + +by the elytral striae less deeply impressed; from + +Bembidion semilotum + +, + +Bembidion ispartanum +Bembidion ispartanum + +, and + +Bembidion siculum +Bembidion durudense + +by the yellow-orange femora with faint brown reflections and by the antennae slightly darkened from the fourth antennomere; from + +Bembidion ispartanum +Bembidion nairicum + +by the antennae with the first three antennomeres light; from + +Bembidion siculum +Bembidion smyrnense + +and + +Bembidion siculum +Bembidion durudense + +by the structure of the endophallus and the not darkened femora; from + +Bembidion zolotarewi + +by the elytral margins not evidently rounded; from + +Bembidion decorum +Bembidion bodemeyeri + +and + +Bembidion decorum +Bembidion subconvexum + +by the elytra less deeply punctate-sulcate and by the structure of the endophallus; from + +Bembidion sokolowskyi + +(Fig. +4 +) by the less transverse pronotum with base slightly oblique towards the angles and by the femora not darkened. + + + + \ No newline at end of file diff --git a/data/38/4D/FE/384DFEB3FFBCE2FA97C9D3EB373898F3.xml b/data/38/4D/FE/384DFEB3FFBCE2FA97C9D3EB373898F3.xml new file mode 100644 index 00000000000..f153b575005 --- /dev/null +++ b/data/38/4D/FE/384DFEB3FFBCE2FA97C9D3EB373898F3.xml @@ -0,0 +1,90 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part C) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +370 +473 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Cerastium maximum +Linnaeus + +, + +Species Plantarum +1 + +: 439. 1753 + + +. + + + +"Habitat in Sibiria. D. Gmelin." RCN: 3406. + + + + +Lectotype +(Lazkov in Cafferty & Jarvis in +Taxon +53: 1051. 2004): +Gmelin s.n. +, Herb. Linn. No. 603.22 ( +LINN +) + +, see right. + + + + +Current name: + + +Cerastium maximum + +L. + +( +Caryophyllaceae +). + + + + \ No newline at end of file diff --git a/data/38/4F/20/384F2097387D1C46201D363D9B5FDECC.xml b/data/38/4F/20/384F2097387D1C46201D363D9B5FDECC.xml new file mode 100644 index 00000000000..b6c0f8e592c --- /dev/null +++ b/data/38/4F/20/384F2097387D1C46201D363D9B5FDECC.xml @@ -0,0 +1,154 @@ + + + +Flora der Schweiz und angrenzender Gebiete. Band 3. Plumbaginaceae bis Compositae (2 nd edition): Unterfamilie _ tubuliflorae + + + +Author + +Hess, Hans Ernst + + + +Author + +Landolt, Elias + + + +Author + +Hirzel, Rosmarie + +text + +1976 +Birkhaeuser Verlag + + +https://doi.org/10.5281/zenodo.292249 + +book +292249 +10.5281/zenodo.292249 +3-7643-0556-8 + + + +<subSubSection id="C31DDF10E0C3CBF7F1945FC91724A929" pageId="null" pageNumber="417" type="nomenclature"> +<paragraph id="04970161AD4C5338FD9519C13422BB30" pageId="null" pageNumber="417"> +<taxonomicName id="717EBCF73684236E464A38959EB7CD31" class="Magnoliopsida" family="Asteraceae" genus="Cirsium" kingdom="Plantae" order="Asterales" pageId="null" pageNumber="417" phylum="Tracheophyta" rank="species" species="pannonicum"> +<pageBreakToken id="FAF2F97D1C0D3ABD36C285BA65666C59" pageId="null" pageNumber="417" start="start">Cirsium</pageBreakToken> +<normalizedToken id="69F411B7F32AB65B274D0F6390B83862" originalValue="pannónicum" pageId="null" pageNumber="417">pannonicum</normalizedToken> +</taxonomicName> +( +<authorityName id="9FE3986E57683600566A597DBD96B7CE" pageId="null" pageNumber="417">L.</authorityName> +fil.) Link +</paragraph> +</subSubSection> +<subSubSection id="F20C651F2FD2D551C0CA303C8A61BC9F" pageId="null" pageNumber="417" type="vernacular_names"> +<paragraph id="5A07B1BDF36B285942A0D9D9532627DC" pageId="null" pageNumber="417">Ungarische Kratzdistel</paragraph> +</subSubSection> + + + +Ausdauernd, mit +duennem +Rhizom; 30-100 cm hoch. Stengel aufrecht, meist einfach, seltener im obern Teil mit wenigen +Aesten +, unten zerstreut, oben dicht filzig behaart, im untern Teil mit mehrzelligen Haaren, ohne Stacheln, aber + +durch die wenig herablaufenden +Blaetter +oft +gefluegelt +. + +Blaetter +oft steif, +gruen +, unterseits oft zerstreut graufilzig behaart, beiderseits mit mehrzelligen Haaren, + +ungeteilt, kurz und fein stachelig +gezaehnt +und stachelig bewimpert + +( + +Wimpern +kuerzer +als 2 mm + +), die obern +herzfoermig +den Stengel umfassend, die untern gelegentlich am Stengel herablaufend. +Koepfe +einzeln. +Huelle +der +bluehenden +Koepfe +1-1,5 cm lang, braunrot. +Huellblaetter +mit ovaler +Harzdruese +; die +aeussern +mit kurzem, anliegendem, kaum stechendem Stachel. Kronen 1,5-2 cm lang, purpurn. +Fruechte +3-4 mm lang, gelbbraun, ohne Flecken. +Pappus +1-1,5 cm lang. - +Bluete +: Sommer. + + +Zytologische Angaben. 2n += +34: +Material aus Ungarn (Baksay 1956). + + +Standort. +Montan. +Maessig +trockene, kalkreiche +Boeden +in +waermeren +Lagen. Wiesen, +Gebuesche +. + + + +Verbreitung +. +Osteuropaeische +Pflanze: + +Nordwaerts +bis +Mittelrussland +und +Suedpolen +; +westwaerts +bis zur Oder, nach +Maehren +und dem +Alpensuedfuss +entlang bis zum Comersee; +suedwaerts +bis +Rumaenien +, Thrazien, Abruzzen. - Im Gebiet: Comerseegebiet (Corni di Canzo, Grigna), Veltlin (Valdone, Ron) und +suedliche +Bergamasker Alpen; die alten Angaben vom Monte Generoso (s. Comolli 1824) sind zu +bestaetigen +. + + + + \ No newline at end of file diff --git a/data/38/4F/5C/384F5C44B87A54B7A3590588EACBAB70.xml b/data/38/4F/5C/384F5C44B87A54B7A3590588EACBAB70.xml new file mode 100644 index 00000000000..94fb3709a11 --- /dev/null +++ b/data/38/4F/5C/384F5C44B87A54B7A3590588EACBAB70.xml @@ -0,0 +1,150 @@ + + + +Insect collecting bias in Arizona with a preliminary checklist of the beetles from the Sand Tank Mountains + + + +Author + +Johnston, M. Andrew +https://orcid.org/0000-0002-0166-6985 +Biodiversity Knowledge Integration Center, Arizona State University, Tempe, AZ, United States of America +ajohnston@asu.edu + + + +Author + +Waite, Evan S. +https://orcid.org/0000-0001-6877-3964 +Biodiversity Knowledge Integration Center, Arizona State University, Tempe, AZ, United States of America + + + +Author + +Wright, Ethan R +https://orcid.org/0000-0002-9226-5967 +Biodiversity Knowledge Integration Center, Arizona State University, Tempe, AZ, United States of America + + + +Author + +Reily, Brian H. +Biodiversity Knowledge Integration Center, Arizona State University, Tempe, AZ, United States of America + + + +Author + +De Leon, Gilma Juanita +https://orcid.org/0000-0003-0727-4031 +Biodiversity Knowledge Integration Center, Arizona State University, Tempe, AZ, United States of America + + + +Author + +Esquivel, Angela Iran +https://orcid.org/0000-0002-1228-662X +Biodiversity Knowledge Integration Center, Arizona State University, Tempe, AZ, United States of America + + + +Author + +Kerwin, Jacob +https://orcid.org/0000-0002-2072-1935 +Biodiversity Knowledge Integration Center, Arizona State University, Tempe, AZ, United States of America + + + +Author + +Salazar, Maria +https://orcid.org/0000-0002-2709-4639 +Biodiversity Knowledge Integration Center, Arizona State University, Tempe, AZ, United States of America + + + +Author + +Sarmiento, Emiliano +https://orcid.org/0000-0002-3523-3088 +Biodiversity Knowledge Integration Center, Arizona State University, Tempe, AZ, United States of America + + + +Author + +Thiatmaja, Tommy +https://orcid.org/0000-0003-0758-8110 +Biodiversity Knowledge Integration Center, Arizona State University, Tempe, AZ, United States of America + + + +Author + +Lee, Sangmi +https://orcid.org/0000-0002-9636-8242 +Biodiversity Knowledge Integration Center, Arizona State University, Tempe, AZ, United States of America + + + +Author + +Yule, Kelsey +Biodiversity Knowledge Integration Center, Arizona State University, Tempe, AZ, United States of America + + + +Author + +Franz, Nico +https://orcid.org/0000-0001-7089-7018 +Biodiversity Knowledge Integration Center, Arizona State University, Tempe, AZ, United States of America + +text + + +Biodiversity Data Journal + + +2023 + +2023-06-28 + + +11 + + +101960 +101960 + + + + +http://dx.doi.org/10.3897/BDJ.11.e101960 + +journal article +http://dx.doi.org/10.3897/BDJ.11.e101960 +1314-2828-11-e101960 +B479CEE677FA57978AE0EE6220BA7572 + + + + +Argoporis bicolor (LeConte, 1851) + + + +Notes + +Identification reference: +Berry (1980) + + + + \ No newline at end of file diff --git a/data/38/4F/B1/384FB10AE50455CA8C2187E122B0F057.xml b/data/38/4F/B1/384FB10AE50455CA8C2187E122B0F057.xml new file mode 100644 index 00000000000..8e164eb9c32 --- /dev/null +++ b/data/38/4F/B1/384FB10AE50455CA8C2187E122B0F057.xml @@ -0,0 +1,311 @@ + + + +The Trichoptera of Panama. XXV. Eight new country records of caddisflies (Insecta, Trichoptera) + + + +Author + +Armitage, Brian J. +https://orcid.org/0000-0003-3182-1533 +Aquatic Invertebrate Research Group (AIRG), Museo de Peces de Agua Dulce e Invertebrados (MUPAD), Universidad Autonoma de Chiriqui (UNACHI), David, Panama & Sistema Nacional de Investigacion de Panama (SNI), Panama City, Panama +tobikera89@gmail.com + + + +Author + +Aguirre, Yusseff P. +https://orcid.org/0000-0001-5222-7563 +Aquatic Invertebrate Research Group (AIRG), Museo de Peces de Agua Dulce e Invertebrados (MUPAD), Universidad Autonoma de Chiriqui (UNACHI), David, Panama + + + +Author + +Rios Gonzalez, Tomas A. +https://orcid.org/0000-0003-0590-6488 +Aquatic Invertebrate Research Group (AIRG), Museo de Peces de Agua Dulce e Invertebrados (MUPAD), Universidad Autonoma de Chiriqui (UNACHI), David, Panama + + + +Author + +Rodriguez, Viterbo +https://orcid.org/0000-0003-1592-4479 +Aquatic Invertebrate Research Group (AIRG), Museo de Peces de Agua Dulce e Invertebrados (MUPAD), Universidad Autonoma de Chiriqui (UNACHI), David, Panama & CCIMBIO-COIBA, Universidad de Panama - Veraguas, Santiago, Panama + + + +Author + +Blahnik, Roger J. +https://orcid.org/0000-0002-0648-454X +Aquatic Invertebrate Research Group (AIRG), Museo de Peces de Agua Dulce e Invertebrados (MUPAD), Universidad Autonoma de Chiriqui (UNACHI), David, Panama & Department of Entomology, University of Minnesota, St. Paul, MN 55108, USA + + + +Author + +Harris, Steven C. +https://orcid.org/0000-0002-6432-7462 +Aquatic Invertebrate Research Group (AIRG), Museo de Peces de Agua Dulce e Invertebrados (MUPAD), Universidad Autonoma de Chiriqui (UNACHI), David, Panama & Department of Biology, Pennsylvania Western University, Clarion, Clarion, PA 16214, USA + +text + + +Neotropical Biology and Conservation + + +2024 + +2024-04-08 + + +19 + + +1 + + +17 +24 + + + + +http://dx.doi.org/10.3897/neotropical.19.e117513 + +journal article +http://dx.doi.org/10.3897/neotropical.19.e117513 +2236-3777-1-17 +E9256564BB92485A9B6A3FBCEDD962F4 +265759C4BB115D019522288F6111D4C1 + + + + +Mayatrichia ayama Mosely, 1937 + + + +Material examined. + + +Panama +, + +Chiriqui +Province + +• + +; in alcohol; +Cuenca +108, + +Boqueron +District + +, + +Rio +Chirigagua + +, +Puente +antes de llegar al +Hotel Los Delfines +; +8.48139°N +, +82.54788°W +; + +128 m +a.s.l. + +; +UV light trap +; +12 Feb. 2021 +; + +T. +Rios + +, +Y. Aguirre +leg.; MUPADI + +; • + +7 ♂ +; in alcohol; ibid., +13 Mar. 2021 +; MUPADI + +; • + +16 ♂ +; in alcohol; ibid., +12 Apr. 2021 +; MUPADI + +; • + + +; in alcohol; ibid., +18 Apr. 2021 +; MUPADI + +; • + + +; in alcohol; ibid., +Cuenca +104, +Bugaba District +, + +Rio +Gueigala + +, + +La +Concepcion + +; +8.51845°N +, +82.64280°W +; + +209 m +a.s.l. + +; +UV light trap +; +12 Feb. 2021 +; leg. + +T. +Rios + +, +Y. Aguirre +leg.; MUPADI + +; • + +12 ♂ +; in alcohol; ibid., +12 Mar. 2021 +; MUPADI + +; • + +17 ♂ +; in alcohol; ibid., +12 Apr. 2021 +; MUPADI + +; • + +10 ♂ +; in alcohol; ibid., +Cuenca +108, +David District +, + +Rio +Platanal + +, +San Pablo Viejo +, puente +via +Interamericana +antes de llegar a la entrada de +Bagala +; +8.46416°N +, +82.52030°W +; + +84 m +a.s.l. + +; +UV light trap +; +6 Oct. 2021 +; leg. + +T. +Rios + +, +Y. Aguirre +leg.; MUPADI + +; • + +6 ♂ +; in alcohol; ibid., +David +, +Via +a +Mantilla +cerca del cementera de +San Pablo Viejo +, +Quebrada del Tejar +; +8.463110°N +, +82.469554°W +; +UV light trap +; +4 Mar. 2022 +; leg. + +T. +Rios + +; MUPADI + +. + + + +Distribution. +Canada, Costa Rica, Honduras, Mexico, Nicaragua, Panama, U.S.A. New country record. + + +Remark. +In Panama, this species was most commonly collected in large, lowland rivers. + + +Subfamily +Stactobiinae +Botosaneanu, 1956 + + + + +Tribe +Stactobiini +Botosaneanu, 1956 + + + + + \ No newline at end of file diff --git a/data/38/4F/CD/384FCDAC968057658185404F3307518B.xml b/data/38/4F/CD/384FCDAC968057658185404F3307518B.xml new file mode 100644 index 00000000000..31daffe500e --- /dev/null +++ b/data/38/4F/CD/384FCDAC968057658185404F3307518B.xml @@ -0,0 +1,88 @@ + + + +Floristic inventory and distribution characteristics of algific talus slopes in a specific area of forest biodiversity in South Korea + + + +Author + +Lee, Jong-Won +https://orcid.org/0000-0002-8687-8396 +Korea National Arboretum, Yanggu, Republic of Korea + + + +Author + +Yun, Ho-Geun +Korea National Arboretum, DMZ Forest Biological Conservation, Yanggu-gun, Republic of Korea + + + +Author + +Hwang, Tae Young +Korea National Arboretum, DMZ Forest Biological Conservation, Yanggu-gun, Republic of Korea + + + +Author + +Kim, Kyungmin +Daoneco, Sejong-si, Republic of Korea + + + +Author + +Jung, Se-Hoon +Daoneco, Sejong-si, Republic of Korea + + + +Author + +An, Jong Bin +Korea National Arboretum, DMZ Forest Biological Conservation, Yanggu-gun, Republic of Korea +ajb8825@korea.kr + +text + + +Biodiversity Data Journal + + +2023 + +2023-12-18 + + +11 + + +113952 +113952 + + + + +http://dx.doi.org/10.3897/BDJ.11.e113952 + +journal article +http://dx.doi.org/10.3897/BDJ.11.e113952 +1314-2828-11-e113952 +5B963235F71B550FA1E3BC1F0E590B10 + + + + +Angelica cartilaginomarginata (Makino ex Y.Yabe) Nakai, 1909 + + + +Distribution +Northeast China to Central & South Japan + + + \ No newline at end of file diff --git a/data/38/50/0F/38500F2CB745FFC1FF31FF6AA4C541E3.xml b/data/38/50/0F/38500F2CB745FFC1FF31FF6AA4C541E3.xml new file mode 100644 index 00000000000..38a1458fd1e --- /dev/null +++ b/data/38/50/0F/38500F2CB745FFC1FF31FF6AA4C541E3.xml @@ -0,0 +1,228 @@ + + + +Taxonomic review of Tapiena (Orthoptera: Phaneropteridae: Phaneropterinae), with key to species and new species from Thailand + + + +Author + +Tan, Ming Kai + + + +Author + +Liu, Chunxiang + + + +Author + +Artchawakom, Taksin + +text + + +Zootaxa + + +2015 + +3920 + + +1 + + + +journal volume +10.11646/zootaxa.3920.1.2 +0ae5e027-d588-4b5a-9835-f0b7f9be4c14 +1175-5326 +236803 +6A4779B4-DAE6-4168-9CD4-0F46B871FF66 + + + + + + + +Tapiena denticulata +Tan, Liu, Artchawakom + +new species + + + + +( +Fig. 6 +) + + + + +Material examined. +Holotype +(male): + +Thailand + +, Nakhon Ratchasima, +Sakaerat +Environmental Research Station, open area with light trap, +N14.50765 +, +E101.92772 +, 446.7 ± +9.7 m +, dry evergreen forest, attracted to light trap, coll. M. K. Tan, H. Yeo & S. T. Toh, +27 June 2014 +, 2220 hours ( +SERS +.14.117) ( +ZRC +). + + +Paratypes +: +2 males +. Same locality as +holotype +: open area with light trap, +N14.50788 +, +E101.92765 +, elev. 413.9 ± +5.6 m +, dry evergreen forest, attracted to light trap, coll. M. K. Tan, H. Yeo & S. T. Toh, +23 June 2014 +( +SERS +.14.13); open area with light trap, +N14.50765 +, +E101.92772 +, 446.7 ± +9.7 m +, dry evergreen forest, attracted to light trap, coll. M. K. Tan, H. Yeo & S. T. Toh, +27 June 2014 +, 2220 hours ( +SERS +.14.124) (all +ZRC +). + + + + +Diagnosis. +This species is typical of the genus but differ from all other species by apex of male cercus bladelike, acute and sclerotized, with dorsal margin denticulate. This species is very similar to + +Tapiena cerciata +Hebard, 1922 + +and + +Tapiena stylata +Bey-Bienko, 1935 + +by highly modified male cercus, forming a blade-like structure but differs by male subgenital plate deeply excised between apical lobes and modifications in male cercus. + + + + +Description. +Habitus as shown in +Fig. 6 +A, typical of genus. Generally similar to + +T. sakaerat + + +sp. n. + +but is slightly larger (mean BWL = +48.4 mm +, n = 3) and differ by: head with length circa 0.4 times of pronotum length (n = 3); pronotum circa 1.3 times longer than wide (n = 3), with anterior margin of dorsal plate slightly concave (instead of straight in + +T. sakaerat + + +sp. n. + +) and lateral lobe circa as tall as long (n = 3) ( +Fig. 6 +B); mesosternum triangular but stouter and with more rounded apex. Also differ slightly from + +T. sakaerat + + +sp. n. + +in tegmen venation: radius sector (Rs) originates before middle, with fork only slightly longer than stem. + + +Male. Stridulatory file of left tegmen generally similar to + +T. sakaerat + + +sp. n. + +in shape but differ in measurements and counts: substraight, feebly crescent-shaped, circa +3.1 mm +(n = 1, +paratype +) in length; file with about 24 (n = 1) stout and more widely spaced teeth at the posterior end, with circa 116 (n = 1) densely and evenly spaced elongated teeth (more closely packed at the sides than in the middle) ( +Figs. 6 +C, 6D). Tenth abdominal tergite forms a setose plate apically; plate wider than long, with lateral margins converging inwards and apical margin truncated and slightly emarginated in the middle ( +Figs. 6 +E, 6F). Epiproct concealed beneath tenth abdominal tergite, slightly exposed at the apex; apex tongue-shaped. Cercus elongated and setose; curved dorso-ventrally (when viewed laterally) and inwards (when viewed dorsally) after middle ( +Figs. 6 +E, 6F); apex blade-like, acute and sclerotized, with dorsal margin denticulate ( +Figs. 6 +E–6G). Subgenital plate slender, longer than broad; apical half forms an elongated and narrow shaft; apical margin very narrowly and deeply excised in the middle, laterally produced into two cylindrical lobes ( +Fig. 6 +G); styli long and slender, slightly curved inwards apically, with apex subacute ( +Figs. 6 +F, 6G). + +Female. Unknown. + +Colouration. Generally green when alive, very similar to + +T. sakaerat + + +sp. n. + +( +Fig. 6 +A). + + +Measurements. See +Table 1 +. + + + + +Etymology. +This species name refers to the denticulated margin at the apex of male cercus; derived from the Latin word +denticulata +(= denticulate, +feminine +). + + +Life history. +This species inhabits dry evergreen forest and is attracted to light at night. + + + + \ No newline at end of file diff --git a/data/38/50/0F/38500F2CB749FFCEFF31FA8FA4944540.xml b/data/38/50/0F/38500F2CB749FFCEFF31FA8FA4944540.xml new file mode 100644 index 00000000000..e44a6e05437 --- /dev/null +++ b/data/38/50/0F/38500F2CB749FFCEFF31FA8FA4944540.xml @@ -0,0 +1,252 @@ + + + +Taxonomic review of Tapiena (Orthoptera: Phaneropteridae: Phaneropterinae), with key to species and new species from Thailand + + + +Author + +Tan, Ming Kai + + + +Author + +Liu, Chunxiang + + + +Author + +Artchawakom, Taksin + +text + + +Zootaxa + + +2015 + +3920 + + +1 + + + +journal volume +10.11646/zootaxa.3920.1.2 +0ae5e027-d588-4b5a-9835-f0b7f9be4c14 +1175-5326 +236803 +6A4779B4-DAE6-4168-9CD4-0F46B871FF66 + + + + + + + +Tapiena sakaerat +Tan, Liu, Artchawakom + +new species + + + + +( +Fig. 5 +) + + + + +Material examined. +Holotype +(male): + +Thailand + +, Nakhon Ratchasima, +Sakaerat +Environmental Research Station, along main road near headquarter, +N14.50786 +, +E101.92905 +, elev. 389.9 ± +4.9 m +, dry evergreen forest, attracted to UV light trap, coll. M. K. Tan, H. Yeo & S. T. Toh, +27 June 2014 +, 2143 hours ( +SERS +.14.104) ( +ZRC +). + + + + +Diagnosis. +This species is typical of the genus but differ from all other species by male tenth abdominal tergite strongly produced into two long apical processes; base of tenth abdominal tergite and the two apical processes webbed; with dorsal process of tenth abdominal tergite curved ventrally (in lateral view) and tapering into an acute apex (in lateral and lateral views); and ventral process of tenth abdominal tergite produced ventrad at the base of dorsal process, bent slightly in the middle (in lateral view), slightly tapering posteriorly, apex forked into two acute lobes (in dorsal view). It also differs from all known species by male cercus with two large inner teeth at apex, both beak-shaped and about the same size. This species is very similar to + +Tapiena ensigera +Karny, 1923 + +by apical process of male tenth abdominal tergite tapering into an acute apex (in dorsal view) and male cercus with two apical spines but differs by male tenth abdominal tergite laterally compressed with dorsal and ventral apical processes webbed. + + + + +FIGURE 3. +Male subgenital plates in ventral views of + +Tapiena stridulous + +(A), + +Tapiena hainanensis + +(B), + +Tapiena longzhouensis + +(C), + +Tapiena javanica + +(D), + +Tapiena bilobata + +(E), + +Tapiena stylata + +(F), + +Tapiena cerciata + +(G), and + +Tapiena simplicis + +(H). Line drawings redrawn from figures from Hebard (1922), Karny (1923), Bey-Bienko (1935), Liu & Kang (2010). + + + + +Description. +Habitus as shown in +Fig. 5 +A, typical of genus. Head with length circa 0.5 times of pronotum length (n = 1, dried specimen, +holotype +). Fastigium short, feebly furrowed in the middle, about as wide as antennal scapus; with apex roundly truncated. Eye prominent; median ocellus round and large. Frons slightly punctuated. Pronotum circa 1.2 times longer than wide (n = 1, dried specimen, +holotype +), densely punctuated. Dorsal plate with anterior margin straight; lateral margins straight and parallel; posterior margin broadly rounded; hind lobe after middle, separated by shallow suture. Lateral keel present. Lateral lobe circa 1.1 times taller than long (n = 1, dried specimen, +holotype +), ventral margin short and pointing ventrad posteriorly, and posterior margin broadly rounded; anterior margin straight, posterior margin feebly convex ( +Fig. 5 +B). Prosternum unarmed. Mesosternum triangular with rounded to subacute apex; metasternum rectangular with posterior angle 90 ° and rounded. Tegmen and hind wing fully developed. Tegmen with anterior and posterior margins feebly convex, apex rounded. Tegminal venation: Radius sector (Rs) originates before middle, with fork distinctively longer than stem; veins and veinlets form small polygonal cells ( +Fig. 5 +A). +Hind +wing with apex distinctively projecting beyond tegmen; exposed apex with ventral margin slightly curved and dorsal margin straight. Legs generally with very short and fine setae. Anterior coxa with distinct but short spine. Anterior tibia with external tympanum open, oval; internal tympanum slit covered by large conchate swelling. + + + +FIGURE 4. +Male cercus in dorsal views (all except G, H) of + +Tapiena bilobata + +(A), + +Tapiena longzhouensis + +(B), + +Tapiena spinicaudata + +(C), + +Tapiena parapentagona + +(D), + +Tapiena quadridens + +(E), + +Tapiena bivittata + +(F), + +Tapiena stylata + +(in lateral view, G), + +Tapiena cerciata + +(in lateral view, H), and + +Tapiena simplicis + +(I). Line drawings redrawn from figures from Karny (1923, 1926b), Bey-Bienko (1935), Liu & Kang (2010). + + + +Male. Stridulatory file of left tegmen substraight, feebly crescent-shaped, circa +2.8 mm +(n = 1, +holotype +) in length; file with about 21 (n = 1) stout and more widely spaced teeth at the posterior end, with circa 140 (n = 1) densely and evenly spaced elongated teeth (more closely packed at the sides than in the middle) ( +Figs. 5 +C, 5D). Tenth abdominal tergite, in dorsal view, basally concave at the sides, in the middle swollen and strongly produced into two long processes ( +Fig. 5 +E). Base of tenth abdominal tergite and the two apical processes webbed ( +Figs. 5 +E, 5F). Dorsal apical process of tenth abdominal tergite curved ventrally (in lateral view) and tapering into an acute apex (in lateral and dorsal views) ( +Figs. 5 +E, 5F). Ventral process of tenth abdominal tergite produced ventrad at the base of dorsal process, bent slightly in the middle (in lateral view) ( +Fig. 5 +F); slightly tapering posteriorly, apex forked into two acute lobes (in dorsal view) ( +Fig. 5 +E). Epiproct concealed beneath tenth abdominal tergite. Cercus cylindrical and setose, slightly curved inwards at the apex; apex with two large inner teeth, both beak-shaped and about the same size ( +Figs. 5 +E, 5F). Subgenital plate with apical margin triangularly and deeply excised in the middle, laterally extended into two long and narrow lobes; styli long and slender, longer than apical lobe and half of length of subgenital plate, tapering into a narrowly obtuse apex ( +Fig. 5 +F). + +Female. Unknown. + +Colouration. Generally green when alive ( +Fig. 5 +A). Head, including frontal rostrum and frons, generally green; gena yellow green; mouth parts, including maxillary palps and mandibles, pale green. Pronotum generally green. Head behind eyes and pronotum with lateral keel with yellow longitudinal band. Tegmen green. +Hind +wings hyalinous, with exposed part green. Fore and middle legs generally pale green: forefemur slightly brown around tympanal area; midfemur darker green at knee. Thoracic segments pale green; abdominal segments yellow or yellow green; abdominal apex mostly pale green to slightly pale yellow green, subgenital plate and cercus pale green. + + +Measurements ( +holotype +, in mm). BL = 26.7; BWL = 43.2; PL = 5.0; PW = 4.2; TL = 34.5; HWT = 3.9; HFL = 17.8; HTL = 18.4. + + + + +Etymology. +This species is named after the +type +locality, +Sakaerat +Environmental Research Station; noun in apposition. + + +Life history. +This species inhabits dry evergreen forest and is attracted to UV light at night. + + + + \ No newline at end of file diff --git a/data/38/50/0F/38500F2CB74CFFC8FF31FC70A49540AF.xml b/data/38/50/0F/38500F2CB74CFFC8FF31FC70A49540AF.xml new file mode 100644 index 00000000000..d51f616fe03 --- /dev/null +++ b/data/38/50/0F/38500F2CB74CFFC8FF31FC70A49540AF.xml @@ -0,0 +1,82 @@ + + + +Taxonomic review of Tapiena (Orthoptera: Phaneropteridae: Phaneropterinae), with key to species and new species from Thailand + + + +Author + +Tan, Ming Kai + + + +Author + +Liu, Chunxiang + + + +Author + +Artchawakom, Taksin + +text + + +Zootaxa + + +2015 + +3920 + + +1 + + + +journal volume +10.11646/zootaxa.3920.1.2 +0ae5e027-d588-4b5a-9835-f0b7f9be4c14 +1175-5326 +236803 +6A4779B4-DAE6-4168-9CD4-0F46B871FF66 + + + + + + +Genus + +Tapiena +Bolívar, 1906 + + + + + + + +Type +species: + +Tapiena acutangula +Brunner + +von Wattenwyl, 1878 + + + + +Diagnosis. +Fastigium frontis with apex as wide as antennal scapus. Head and pronotum densely punctuated. Tegmen without distinct Costal vein. Fore coxa armed with a spine. Fore tibia with external tympanum open, oval; internal tympanum slit covered by large conchate swelling. +Hind +femur with genicular lobe rounded, without any spine. Male subgenital plate with styli long, as long as half the length of subgenital plate. Ovipositor with lateral surface not granuliferous, with dorsal and ventral margins finely serrulated ( +Liu & Kang, 2010 +). + + + + \ No newline at end of file diff --git a/data/38/50/0F/38500F2CB74CFFCBFF31FAF1A5C241F2.xml b/data/38/50/0F/38500F2CB74CFFCBFF31FAF1A5C241F2.xml new file mode 100644 index 00000000000..8e5945e91db --- /dev/null +++ b/data/38/50/0F/38500F2CB74CFFCBFF31FAF1A5C241F2.xml @@ -0,0 +1,485 @@ + + + +Taxonomic review of Tapiena (Orthoptera: Phaneropteridae: Phaneropterinae), with key to species and new species from Thailand + + + +Author + +Tan, Ming Kai + + + +Author + +Liu, Chunxiang + + + +Author + +Artchawakom, Taksin + +text + + +Zootaxa + + +2015 + +3920 + + +1 + + + +journal volume +10.11646/zootaxa.3920.1.2 +0ae5e027-d588-4b5a-9835-f0b7f9be4c14 +1175-5326 +236803 +6A4779B4-DAE6-4168-9CD4-0F46B871FF66 + + + + + + +Key to species of + +Tapiena + +(for males only) + + + + + +Tapiena emarginata +Karny, 1923 + +, + +Tapiena latifolia +Ingrisch & Shishodia, 2000 + +, + +Tapiena pentagona +Karny, 1923 + +and + +Tapiena triangulata +Karny, 1926 + +are only known for females and thus not included in this key. This key is modified from key for +China +species by +Liu & Kang (2010) +. + + + + + + +1. Distribution: Africa................................................................... + +T. minor +Bolívar, 1906 + + + + +- Distribution: Asia..................................................................................... 2 + + + + + +2. Distribution: +India +............... + +T. acutangula + +(Brunner von Wattenwyl, 1878) or + +T. latifolia +Ingrisch & Shishodia, 2000 + + + + + +- Distribution: +China +and Southeast Asia.................................................................... 3 + + + + + + +3. Tenth abdominal tergite with apical process highly modified into a large laterally compressed plate (Figs. 1A– +1I +, 5F)...... 4 + + + +- Tenth abdominal tergite simple, with little or no modification, often forming a simple plate (not laterally compressed) (Figs. 1J–1L, 6E, 6F)....................................................................................... 13 + + + + + +4. Apical process of tenth abdominal tergite bilobate apically (in dorsal view) ( +Figs. 2 +A–2E)............................ 5 + + + + +- Apical process of tenth abdominal tergite not furrowed or bifurcate apically, often tapering into an acute, obtuse or truncated apex (in dorsal view) ( +Figs. 2 +F–2H, 5E).................................................................... 9 + + + + + + +5. Subgenital plate with stylus distinctively longer than apical lobe ( +Figs. 3 +A, 3B).................................... 6 + + + + +- Subgenital plate with stylus about same length as, or only slightly longer than apical lobe ( +Figs. 3 +C–3E)................ 7 + + + + + + +6. Stridulatory file on left tegmen with about 240 fine teeth. Apical process of tenth abdominal tergite with short lobes at apex diverging outwards from one another; excision between lobes broadly rounded (in dorsal view) ( +Fig. 2 +A)............................................................................................. + +T. stridulous +Liu & Kang, 2010 + + + + + +- Stridulatory file on left tegmen with about 150 rather distinct fine teeth and about apical 25 indistinct teeth. Apical process of tenth abdominal tergite with short lobes at apex not diverging outwards from one another; excision between lobes truncated (in dorsal view) ( +Fig. 2 +B).......................................................... + +T. hainanensis +Liu & Xia, 1996 + + + + + + + +7. Apical process of tenth abdominal tergite distinctively forked or bilobate apically (in dorsal view) ( +Figs. 2 +C, 2D); in lateral view, with ventral process pointing ventrad (Figs. 1C, 1D). Cercus more slender and gently curved inwards ( +Fig. 4 +A)..... 8 + + + + +- Apical process of tenth abdominal tergite feebly bilobate apically (in dorsal view) ( +Fig. 2 +E); in lateral view, with ventral process pointing ventrad-posteriorly (Fig. 1E). Cercus more robust with interior margin more concave ( +Fig. 4 +B)............................................................................................. + +T. longzhouensis +Liu, 2004 + + + + + + + +8. Apical process of tenth abdominal tergite tapering to an acute apex, with ventral process short and forked apically (in lateral view) (Fig. 1C); forked into two triangular lobes; excision between lobes subacute (in dorsal view) ( +Fig. 2 +C)................................................................................................ + +T. javanica +Karny, 1926 + + + + + +- Apical process of tenth abdominal tergite blunt, with ventral process long and acute apically (in lateral view) (Fig. 1D); forked into two truncated lobes; excision between lobes rounded (in dorsal view) ( +Fig. 2 +D).......... + +T. bilobata +Liu & Kang, 2010 + + + + + + + +9. Apical process of tenth abdominal tergite with dorsal surface spiniferous in the apical third, with numerous spines along ventral margin (Figs. 1F, 1G). Cercus with two processes at the apex, with a large distal spine and small subapical spine on exterior margin ( +Figs. 4 +C, 4D)................................................................................. 10 + + + +- Apical process of tenth abdominal tergite with dorsal surface not spiniferous; with few or no spines along ventral margin. Cercus not as above...................................................................................... 11 + + + + + +10. Apical process of tenth abdominal tergite with 4–5 spines on ventral margin, apex more blunt (in lateral view) (Fig. 1F)................................................................................ + +T. spinicaudata +Liu & Xia, 1996 + + + + + +- Apical process of tenth abdominal tergite with 2–3 spines on ventral margin, apex more acute (in lateral view) (Fig. 1G)............................................................................ + +T. parapentagona +Liu & Kang, 2010 + + + + + + + +11. Apical process of tenth abdominal tergite forming a triangular ventral process (in lateral view) (Figs. 1H, +1I +, 2G, 2H)...... 12 + + + + +- Apical process of tenth abdominal tergite produced into two long processes, not forming a triangular ventral process (in lateral view) ( +Fig. 5 +F)........................................................................... + +T. sakaerat + + +sp. n. + + + + + + + +12. Apical process of tenth abdominal tergite with apex acute (in lateral view and dorsally) (Figs. 1H, 2G).................................................................................... + +T. cucullata + +(Brunner von Wattenwyl, 1891) + + + + +- Apical process of tenth abdominal tergite with apex truncated (in lateral view and dorsally) (Fig. +1I +, 2H)............................................................................................... + +T. yunnana +Xia & Liu, 1990 + + + + + + + +13. Tenth abdominal tergite with teeth or long process apically (in dorsal view) ( + +Figs. +2 + +I, 2J)............................ 14 + + + +- Tenth abdominal tergite without tooth or long process apically (in dorsal view)................................... 15 + + + + + +14. Tenth abdominal tergite with a long process that tapers into an acute apex (Figs. 1J, +2I +). Cercus simple with two small apical spines (Figs. 1J, +2I +).................................................................. + +T. ensigera +Karny, 1923 + + + + + +- Tenth abdominal tergite with four teeth apically, two lateral and two medial teeth (in dorsal view) ( +Fig. 2 +J). Cercus with interior margin inflated from middle with apex forming a wide compressed tooth ( +Fig. 4 +E)...... + +T. quadridens +Liu & Xia, 1996 + + + + + + + +15. Cercus simple, bent inwards apically into an acute apex ( +Fig. 4 +F).......................... + +T. bivittata +Xia & Liu, 1992 + + + + + +- Cercus modified (Figs. 1K, 1L, 4G– +4I +, 6E–6G)............................................................. 16 + + + + + +16. Tenth abdominal tergite excised in the middle, to form two lobes............................................... 17 + + +- Tenth abdominal tergite not excised in the middle........................................................... 18 + + + + + +17. Cercus with apex forming a broad, ovate node (Fig. 1K)...................................... + +T. bullata +Karny, 1923 + + + + + +- Cercus distinctively bilobate apically with obtuse inner tooth (Fig. 1L)........................... + +T. incisa +Karny, 1923 + + + + + + + +18. Cercus elongated; with apex acute and sclerotized, with dorsal margin denticulate ( +Figs. 6 +F, 6G). Subgenital plate deeply excised between apical lobes ( +Fig. 6 +G)...................................................... + +T. denticulata + + +sp. n. + + + + + +- Cercus not as above. Subgenital plate not deeply excised between apical lobes ( +Figs. 3 +F–3H)........................ 19 + + + + + + +19. Cercus more with more than apical half lamellate, narrowing into an apex that recurved dorsally ( +Figs. 4 +G, 4H).......... 20 + + + + +- Cercus apical part enlarged apically, with an upcurved hook ( + +Fig. +4 + +I)....................... + +T. simplicis +Liu & Xia, 1996 + + + + + + + +20. Cercus with a lamellate appendage pointing dorsally in the middle ( +Fig. 4 +G). Subgenital plate with posterior margin triangularly excised between the lobes ( +Fig. 3 +F)............................................. + +T. stylata +Bey-Bienko, 1935 + + + + + +- Cercus without a lamellate appendage pointing dorsally in the middle ( +Fig. 4 +H). Subgenital plate with posterior margin roundly excised between the lobes ( +Fig. 3 +G)............................................. + +T. cerciata +Hebard, 1922 + + + + + + + \ No newline at end of file diff --git a/data/38/50/95/3850957D26CC515C8B9F8E04D7F6B511.xml b/data/38/50/95/3850957D26CC515C8B9F8E04D7F6B511.xml new file mode 100644 index 00000000000..5a816f6ac04 --- /dev/null +++ b/data/38/50/95/3850957D26CC515C8B9F8E04D7F6B511.xml @@ -0,0 +1,132 @@ + + + +Psychodidae (Diptera) of Azerbaijan and Georgia - faunistics with biodiversity notes + + + +Author + +Jezek, Jan +Department of Entomology, National Museum, Cirkusova 1740, CZ - 193 00 Praha 9 - Horni Pocernice, Czech Republic + + + +Author + +Manko, Peter +https://orcid.org/0000-0003-1862-9117 +Department of Ecology, Faculty of Humanities and Natural Sciences, University of Presov, 17. novembra 1, SK - 081 16 Presov, Slovakia +peter.manko@unipo.sk + + + +Author + +Obona, Jozef +https://orcid.org/0000-0002-1185-658X +Department of Ecology, Faculty of Humanities and Natural Sciences, University of Presov, 17. novembra 1, SK - 081 16 Presov, Slovakia + +text + + +ZooKeys + + +2021 + +2021-06-15 + + +1049 + + +15 +42 + + + + +http://dx.doi.org/10.3897/zookeys.1049.66063 + +journal article +http://dx.doi.org/10.3897/zookeys.1049.66063 +1313-2970-1049-15 +E0AEB4DB6C32407697542AA74386C517 +F43B77514DD55AC69BA1E334AE61ABF2 + + + + +Logima sigma (Kincaid, 1899) + + + +Material examined. + + + +Azerbaijan + +: A 22, +5.5.2019 +, +1♀ +, slide +Inv. No. +25626, leg. JO (Fig. +2 +) + +. + + + +Distribution. + +Uncommon Holarctic species. Recorded from Austria, Belgium, Czech Republic, France, Great Britain, Norway, Poland, Slovakia, Spain (incl. Madeira); Antipodes Is., Auckland L. (lake or lakes), Australia, Campbell L., Chile, Enderby L., Ewing L., French L., Macquarie L., New Zealand, Ocean L., Rose L., Saint Helena, and USA ( + +Andersen and +Haland +1995 + +; + +Jezek +2003 + +; +Kvifte et al. 2011 +; +Kvifte and Andersen 2012 +; + +Elgueta and +Jezek +2014 + +; +Haselboeck 2016 +; + +Jezek +et al. 2018 + +b; + +Obona +and +Kozanek +2018 + +; +Wagner 2018 +). + + + +Note. +First record for Azerbaijan and Transcaucasia. + + + \ No newline at end of file diff --git a/data/38/50/9B/38509B66A338AE609B03A30D9E0F23FE.xml b/data/38/50/9B/38509B66A338AE609B03A30D9E0F23FE.xml new file mode 100644 index 00000000000..6d730542624 --- /dev/null +++ b/data/38/50/9B/38509B66A338AE609B03A30D9E0F23FE.xml @@ -0,0 +1,200 @@ + + + +Revision of the genus Reinmara Schaus, 1928 (Lepidoptera, Mimallonoidea, Mimallonidae) with the descriptions of four new species from South America + + + +Author + +Laurent, Ryan A. St + + + +Author + +Herbin, Daniel + + + +Author + +Mielke, Carlos G. C. + +text + + +ZooKeys + + +2017 + +677 + + +97 +129 + + + + +http://dx.doi.org/10.3897/zookeys.677.12435 + +journal article +http://dx.doi.org/10.3897/zookeys.677.12435 +1314-2003-677-97 +47DDCEE5B65C495D83DE0D2016A0F5D2 + + + + +Reinmara andensis +sp. n. +Figs 9-11, 25, 36 + + + +Type material. + +Holotype, ♂. BOLIVIA: BOLIVIE, N. Yungas, 1000-1800 m, Oct,nov,Dec,2008, Leg. local collector for R. Marx, Coll. D. Herbin/ genitalia prep. D. Herbin ref H. 1134/ HOLOTYPE male +Reinmara andensis +St Laurent, Herbin, & C. Mielke, 2017 [handwritten red label]/ (MNHN). Type locality: Bolivia, northern Yungas [no specific locality provided on data label]. + + + +Paratypes. + +(9 ♂ total) BOLIVIA: 1 ♂, same data as for holotype (CDH). La Paz: 1 ♂, Nor [North] Yungas, Road Caranavi-Coroico, ca. 100 km NE La Paz, ca. +16.2°S +, +67.6°W +, 1000-1800 m: +V-VI +.2009, R. Brechlin & F. Meister leg. (MWM). 1 ♂, +Rio +Songo [recte +Rio +Zongo], 750 m: ex-Coll. Fassl, NHRS-TOBI 1951 (NHRS). PERU: Puno: 1 ♂, Santo Domingo, Carabaya, 6000 ft: I.1902, wet season, Ockenden [leg.], Rothschild Bequest, BM 1939-1, NHMUK01354562 (NHMUK). 1 ♂, Locality as for previous but: VI.1902, dry season, NHMUK 010318284 (NHMUK). 2 ♂, La Oroya [Oroya], +Rio +Inambari, 3100 ft: III.1905, +XI-XII +.1905, wet season, G. Ockenden [leg.], Rothschild Bequest, BM 1939-1, NHMUK010354561, St Laurent diss.: 11-1-16:9 (NHMUK). 2 ♂, Locality and collector as for previous but: 3000 ft, V.1905, Ex-Coll. +Oberthuer +, Brit. Mus. 1927-3, NHMUK010354560 (NHMUK). + + + +Specimens of uncertain identity hereby excluded from the type series + +. ECUADOR: Napo: 1 ♂, 1 ♀, Wildsumaco Biol. Stat., E slope Andes Mtns, +0°40'17.2"S +, +77°35'55.1"W +, ~1400 m: 1-14.VIII.2016, Kawahara + Barber Labs et al. leg., DNA voucher numbers LEP-40632, 42829 (MGCL, molecular collection, barcoded). PERU: San +Martin +: 1 ♂, Mina de Sal, 1400 m: V.2007, Rainer Marx leg., Genitalia prep. No. 29.219 MWM (MWM). +Huanuco +: 1 ♂, Leoncio Prado, La Divisoria, 1600 m: 20.VI.1982, Charles F. Zeiger [leg.] (MGCL). + + + +Diagnosis. + +Reinmara andensis +is similar to +R. enthona +but larger, with broader wings and broader submarginal areas, which are more uniformly light brown. Medially the light gray scaling is reduced in comparison with +R. enthona +. The genitalia are very similar to those of +R. enthona +, but are overall somewhat larger, the gnathos extensions are shorter and phallus more tubular with a more protruding ventral distal lip in comparison with +R. enthona +. The lower right diaphragm sac is larger and more ovoid in shape in +R. andensis +, in +R. enthona +it is smaller and more spherical. + + + +Description. + +Male.Head: As for genus, but light brown in color. Thorax: Coloration as for head. Legs: Coloration as for thorax, vestiture thick, long. Forewing dorsum: Forewing length: 18.5-20.0 mm, avg.: 19.2 mm, wingspan: 37-40 mm, n=5. Triangular, margin slightly concave below apex; tornus notched, apex hardly falcate. Ground color light orange-brown, very sparsely scattered with tiny, dark brown, petiolate scales. Ante- and medial areas appearing lighter brown than more uniformly orange-brown submarginal area due to suffusion of lighter gray scales medially, especially near costa and on inner side of postmedial line, in some specimens medial area may be very dark brown with less suffusion of grayish pink. Antemedial line almost nonexistent. Discal mark pale gray, ovoid, variously darkened at center. Fringe coloration lighter than wing margin with nearly white trailing edge. Forewing ventrum: Similar to dorsum but more homogenously brown overall due to reduction in paler gray shading. Antemedial line absent, postmedial line reduced to traces. Hindwing dorsum: Notch on anterior margin weak, patterning as for forewing dorsum, but antemedial line absent, discal mark and postmedial line weakly defined. Hindwing ventrum: Following same pattern as forewing ventrum but traces of postmedial line outwardly bent mesally. Abdomen: Coloration as for thorax. Genitalia: (Fig. 25) n=4. Typical of genus, very similar to that of +R. enthona +but overall larger structures, with shorter but more robust gnathos extensions and a more tubular phallus with more prominent ventral distal lip. Female. Unknown [putative female from Wildsumaco, Napo, Ecuador does not differ from female +R. enthona +]. + + + +Distribution + +(Fig. 36). +Reinmara andensis +is an Andean species present in southeastern Peru in the Puno region, as well as northwestern Bolivia. Other records from north central Peru in San +Martin +and +Huanuco +as well as eastern Ecuador may represent this or additional cryptic Andean taxa. + + + +Etymology. +This new species is named for its Andean distribution. + + +Remarks. + +Additional material from MWM and MGCL from other localities in Peru besides those from the Puno region need verification due to the unreliability of the collector and/or unclear collecting data. We anticipate that this new species is more broadly distributed, but considering the close similarity to +R. enthona +and unavailability of recently collected Peruvian material, we restrict the type series of this species to include only those from northwestern Bolivia and adjacent southeast Peru. Although +R. andensis +is endemic to the eastern slopes of the Andes, it appears to be sympatric with +R. enthona +at the lower elevations in the inhabited range of +R. andensis +. + + +Due to the barcoding results (Fig. 7) and biogeography placing an Ecuadorian specimen (Lep-40632) closer to +R. andensis +, we have included specimens from this location under additional examined material for +R. andensis +, though they are excluded from the type series pending additional information. Furthermore, these barcoding results are not clear in that +R. wolfei +(Bc-Her4822) is nested within the clade including +R. andensis +and the Ecuadorian +R. cf andensis +, with low bootstrap support. Morphology certainly suggests that +R. enthona +and +R. andensis +are more similar than the rather +unique +, +R. wolfei +. Additional molecular and morphological data will be required to fully elucidate the relationships within +Reinmara +. We do not consider single genes, particularly COI, to offer significant phylogenetic signal, especially considering recent work refuting species delimitation based on genetic evidence alone ( +Sukumaran and Knowles 2017 +), thus we include the tree in Fig. 7 merely as additional evidence differentiating the Amazonian +R. enthona +from the externally similar Andean +R. andensis +. + + +In the NHMUK, the Peruvian specimens were collected both during the "dry season" and "wet season" with those specimens from the dry season being smaller overall than those from the wet season. No significant genitalia differences were noted between these sets of specimens however. +Reinmara andensis +is generally larger than +R. enthona +but dry season +R. andensis +are much closer in size to those of +R. enthona +. + + + + \ No newline at end of file diff --git a/data/38/50/C2/3850C2BBA3A04A218DC997392FA02ADF.xml b/data/38/50/C2/3850C2BBA3A04A218DC997392FA02ADF.xml new file mode 100644 index 00000000000..b06072c9cce --- /dev/null +++ b/data/38/50/C2/3850C2BBA3A04A218DC997392FA02ADF.xml @@ -0,0 +1,196 @@ + + + +A systematic revision of Operclipygus Marseul (Coleoptera, Histeridae, Exosternini) + + + +Author + +Caterino, Michael S. + + + +Author + +Tishechkin, Alexey K. + +text + + +ZooKeys + + +2013 + +271 + + +1 +401 + + + + +http://dx.doi.org/10.3897/zookeys.271.4062 + +journal article +http://dx.doi.org/10.3897/zookeys.271.4062 +1313-2970-271-1 + + + + +Operclipygus marginellus (LeConte, 1860) +comb. n. +Figs 80A81 +A-D +, GMap 29 + + + + +Phelister marginellus +J.E. +LeConte 1860 +: 311; +Tribalister marginellus +: +Horn 1873 +: 299. + + + +Type locality. +Not specified beyond Maryland State, USA. + + +Type material. + +Lectotype, herein designated: +"Maryland" +/ " +Phelister marginata +[sic]" / " +Tribalister marginellus +Horn (Lec.)" / "MCZ Type 35024" / "Aug.-Dec.2004 MCZ Image Database" / "LECTOTYPE +Phelister marginellus +LeC. M.S. Caterino & A.K. Tishechkin des. 2010" (MCZC). This species was described from an unspecified number of specimens, and the lectotype designation fixes primary type status on the only known original specimen. + + + +Other material. + +USA: Florida: 1: Levy Co., 4.0 mi. SW Archer, +29°30'10"N +, +82°24'23"W +, 19-26.iv.2000, P. Skelley, barrier pitfall trap (FSCA), 1: 13-25.vii.2000, 1: 18-21.v.1988, P. Skelley, window trap in rosemary, turkey oak sandhill (FSCA); 1: Alachua Co., 5.v.1993, R. Lundgren, flight barrier trap in hardwood hammock (CHPWK), 1: 18.vii.1994 (AKTC), 2: 18.vi.1995 (CHPWK); 1: Polk Co., Lake Marion Creek Estates, FIT, 26.x-9.xi.1999, R. Morris, FIT (AKTC). Texas: 1: Angelina Co., Angelina NF, ~3mi. NE Rockland, +31°3'19"N +, +94°22'06"W +, 19.ix-2.x.1996, Clarke, +Menard +, Riley, pitfall, unmanaged longleaf pine (TAMU). Wisconsin: 1: Sauk Co., Spring Green Preserve SNA, +43°11'58"N +, +90°03'32"W +, 12.vii.2003, J.P. Gruber, in nest +Aphaenogaster +sp., under rock on bluff prarie (CHJG), 1: 17.vi.2000, attached to +leg +of live +Aphaenogaster treatae +Forel, under board in sandy oak barren (CHJG), 1: 19-30.v.2001, J.P. Gruber, FIT, 1: 30.v-16.vi.2001, J.P. Gruber, FIT (CHJG). + + + +Diagnostic description. + +Length: 1.68-1.75 mm, width: 1.50-1.55 mm; body rufescent, broadly rounded, strongly convex, with very fine granulate microsculpture on most surfaces; frons broad, weakly depressed at middle, sides of frontal stria rounded, curving evenly, transverse across front; supraorbital stria complete, connected to sides of frontal stria; epistoma weakly depressed, slightly elevated at sides, weakly emarginate apically; labrum about 2.5 +x +as wide as long, flat, weakly emarginate apically; left mandible with broad, blunt basal tooth, right with slightly smaller, subacute tooth; pronotum lacking prescutellar impression, with only very faint, shallow lateral punctures; marginal pronotal stria continuous along all edges; lateral submarginal pronotal stria complete, close to margin, subcarinate, continuous with anterior submarginal stria, pronotal disk depressed along their inner edges; median pronotal gland openings faintly annulate, located about two-thirds pronotal distance behind anterior margin; elytron with two complete, crenulate epipleural striae, outer subhumeral stria carinate, forming lateral elytral margin continuous with lateral pronotal margin, inner subhumeral stria absent, dorsal striae 1-5 complete, rather broadly depressed, with outer edge of stria strongly carinate, sutural stria obsolete in basal third, similarly deeply impressed, all striae converging toward midline apically; elytral disk with numerous coarse punctures near apical margin; prosternal keel truncate at base, with carinal striae complete, divergent and free basally and apically; prosternal lobe very short, with marginal stria weak to obsolete; mesoventrite broadly and shallowly emarginate along anterior margin, with marginal stria very close to margin, weak at middle; mesometaventral stria broadly arched forward to anterior mesoventral margin, meeting inner corner of mesocoxa at side, continued by lateral metaventral stria which extends laterally, parallel to postmesocoxal stria, strongly abbreviated; metaventrite moderately convex; 1st abdominal ventrite with two lateral striae, depressed along complete inner lateral stria, outer stria obsolete basally; propygidium uniformly and densely covered with coarse punctures; pygidium with fewer and sparser punctures, mainly at sides, impunctate toward apex; marginal pygidial sulcus well impressed along most of margin, obsolete toward base. Male genitalia (Figs 81 +A-D +, G): accessory sclerites present; T8 short, with sides subparallel in basal two-thirds, abruptly narrowed to apex, apical emargination narrow, basal emargination nearly reaching basal membrane attachment line, ventrolateral apodemes evenly developed to base and apex, nearly meeting along midline; S8 elongate, subparallel, with apical guides well developed throughout most of length, ventral edges divergent to apex; T9 with sides subparallel in basal third, convergent to apex, apices narrow, opposing; T10 with halves fully separate; S9 broadened in basal half, weakly rounded at base, lacking apical emargination, apical flange entire; tegmen narrow, with sides rounded, widest just basad midpoint, ventromedial projection weak, +'U' +-shaped, barely projecting beneath about one-fourth from base; median lobe about one-third tegmen length, proximal apodemes not obviously differentiated; basal piece almost one-half tegmen length. + + + + +Remarks +. + + +The two Nearctic species of the +Operclipygus marginellus +group are easily distinguished. +Operclipygus marginellus +has distinctly carinate elytral striae (Fig. 80A), whereas those of +Operclipygus striatellus +are merely deeply impressed (Fig. 80B). + + + +Figure 80. Various +Operclipygus marginellus +group species. A Dorsal habitus of +Operclipygus marginellus +B Dorsal habitus of +Operclipygus striatellus +C Pronotum of +Operclipygus striatellus +D Dorsal habitus of +Operclipygus formicatus +E Ventral habitus of +Operclipygus formicatus +F Pygidia of +Operclipygus formicatus +G Dorsal habitus of +Operclipygus hintoni +H Ventral habitus of +Operclipygus hintoni +. + + + + +Figure 81. Male genitalia of +Operclipygus marginellus +group species. A T8 of +Operclipygus marginellus +B S8 of +Operclipygus marginellus +C T9 & T10 of +Operclipygus marginellus +D S9 of +Operclipygus marginellus +E S9 of +Operclipygus striatellus +F S8 of +Operclipygus striatellus +G Aedeagus, dorsal and lateral views, of +Operclipygus marginellus +H Aedeagus, dorsal and lateral views, of +Operclipygus hintoni +I T8 of +Operclipygus striatellus +J T8 of +Operclipygus hintoni +K S8 of +Operclipygus hintoni +L S9 of +Operclipygus hintoni +. + + + + +Map 29. Records of the +Operclipygus marginellus +group. + + + + + \ No newline at end of file diff --git a/data/38/51/0D/38510DF88AE66728C2924F9DDA01F10A.xml b/data/38/51/0D/38510DF88AE66728C2924F9DDA01F10A.xml new file mode 100644 index 00000000000..baf33538be7 --- /dev/null +++ b/data/38/51/0D/38510DF88AE66728C2924F9DDA01F10A.xml @@ -0,0 +1,348 @@ + + + +A monograph of the genus Polylepis (Rosaceae) + + + +Author + +Boza Espinoza, Tatiana Erika +https://orcid.org/0000-0002-9925-1795 +Institute for Nature, Earth and Energy (INTE), Pontificia Universidad Catolica del Peru (PUCP), Av. Universitaria 1801, Lima 15088, Peru +tatianaerika@gmail.com + + + +Author + +Kessler, Michael +https://orcid.org/0000-0003-4612-9937 +Department of Systematic and Evolutionary Botany, University of Zurich, Zollikerstrasse 107, CH- 8008 Zurich, Switzerland + +text + + +PhytoKeys + + +2022 + +2022-08-01 + + +203 + + +1 +274 + + + + +http://dx.doi.org/10.3897/phytokeys.203.83529 + +journal article +http://dx.doi.org/10.3897/phytokeys.203.83529 +1314-2003-203-1 +001CD6EE01E8575F81AC9EFDD0599077 + + + + +43. +Polylepis nana (M.Kessler) T.Boza & M.Kessler, comb. et +stat. nov. + + + + +Figs 110 +, 111 + + + + +Polylepis tomentella subsp. nana +M. +Kessler (1995b +: 166). Type. Based on +Polylepis nana +(M.Kessler) T.Boza & M.Kessler. + + + + +Type +. + + + +Bolivia +. Dept. +Cochabamba +, Prov. Arani, +2 km +W turn-off to +Vacas +from +Arani-Mizque +road, l +7°33'S +, +65°42'W +, + +3200 m + +, +18 Aug1991 +, +Kessler 3409 +( +holotype +: LPB!; isotypes: AUU!, GOET!) + +. + + + +Figure 110. + +Polylepis nana + +(M.Kessler) T.Boza & M.Kessler +A +branching pattern +B +branching pattern. Photographs by M. Kessler. + + + + +Description. + +Shrub +to 2 m tall. +Leaves +slightly congested at the branch tips, imparipinnate with one pair of leaflets, trullate in outline, 1.7-2.4 +x +1.2-1.9 cm; rachises densely villous, points of leaflet attachment with a tuft of long hairs; stipular sheaths apically truncate or slightly spurred, densely villous on the outer surfaces; leaflets obovate in outline, second pair from the terminal leaflet the largest, one of this pair 1.0-1.2 +x +0.3-0.5 cm; margin serrate with 5-8 teeth, apically acute, basally unequally attenuate; upper leaflet surfaces often with dark sheen, glabrous to sparsely villous; lower leaflet surfaces with a dense layer of very short, white or yellowish pannose hairs. +Inflorescences +pendant, 0.9-1.2 cm long, bearing 2-4 flowers; floral bracts 2.4-3.1 mm long, narrowly triangular, densely villous on the outer surface; rachises villous. +Flowers +5.4-6.8 mm diam.; sepals 3, ovate, green, sparsely villous outside; stamens 12-15, anthers orbicular, with a dense tuft of straight white hairs on the upper half; styles fimbriate, 3.0-3.3 mm long. +Fruits +turbinate, with 3-4 irregular flattened ridges with a series of spines, densely villous; 5.0-7.7 +x +3.0-3.3 mm including spines. +Tetraploid +. + + + +Figure 111. + +Polylepis nana + +(M.Kessler) T.Boza & M.Kessler +A +flowering branch +B +stipular sheaths +C +fruit +D +lower leaf surface +E +upper leaf surface ( +A +Kessler 3512 +B +Kessler 3495 +C +Kessler 3513 +D +Kessler 3642 +E +Kessler 3520 +). Scale bars: 8 cm ( +A +); 6 mm ( +C +); 1 cm ( +D, E +). Photographs by T. E. Boza E. + + + + +Distribution, habitat and ecology. + + +Polylepis nana + +is restricted to Cochabamba (Bolivia) where it has been collected at just one locality in Arani Province (Fig. +116 +). It grows at 3200-3450 m elevation. + + + +Conservation status. + +The EOO for + +Polylepis nana + +is estimated as 8 km2, the AOO is assessed at 8 km2 and it is known from only one location. No conservation action has been taken to date. + +Polylepis nana + +was categorized as CR (B1+2c, C2b) in the World List of Threatened Trees ( +Oldfield et al. 1998 +). However, it was classified as EN (B1ab(i,ii,iii)) in the Red List of Threatened Flora of Bolivia ( + +Arrazola +et al. 2012 + +). The only known locality consists of extensive, but heavily degraded stands in the Arani-Vacas area where they are strongly threatened by overgrazing, logging and burning of grasslands. We assess + +P. nana + +as Critically Endangered (A1+A2a, B1a, C1+ C2a, D2a). + + + +Notes. + + +Polylepis nana + +can be distinguished from the most similar species + +P. tomentella + +by its shrubby growth form, smaller leaflets (1.0-1.2 +x +0.3-0.5 cm vs. 1.3-2.0 +x +0.5-0.7 cm) with acute apex (vs. round to slightly emarginated), shorter inflorescences (0.9-1.2 cm vs. 2.8-5.3 cm) with fewer flowers (2-4 vs. 4-5), fewer stamens per flower (12-15 vs. 19-25) and longer styles (3.0-3.3 mm vs. 2.4-2.5 mm). + + + +Specimens examined. + + + +Bolivia +. +Cochabamba + +: +Arani +, + +between Arani and +Canadas + +on the road to +Vacas +, +17°34'S +, +065°40'W +, + +3100 m + +, +20 April 1987 +, +Brandbyge 708 +(AAU!); +Kewinal +, + +3300 m + +, +24 March 1991 +, +Hensen 1949 +(LPB); +2012 +(LPB); +2 km +after turnoff to +Vacas on Mizque-Arani +road, +17°33'S +, +065°42'W +, + +3100 m + +, +18 August 1991 +, +Kessler 2998 +(GOET!, LPB); +2 km +W turnoff to Vacas from Arani-Mizque road, +17°33'S +, +065°42'W +, + +3200 m + +, +18 August 1991 +, +Kessler 3403 +; +3404 +(GOET!, LPB); +3405 +(GOET!); +3406 +; +3407 +(GOET!, LPB); +3408 +(GOET!, LPB, USM!); +3409 +(AAU!, GOET!); +3495 +; +3501 +; +3514 +; +3518 +; +3519 +; +3521 +; +3641 +(GOET!); +3642 +(GOET!); camino a Vacas, + +3170 m + +, +11 January 1990 +, +Saravia 17 +(LPB) + +. + + + + \ No newline at end of file diff --git a/data/38/51/1A/38511AD4D5A84A749725308AF02B1784.xml b/data/38/51/1A/38511AD4D5A84A749725308AF02B1784.xml new file mode 100644 index 00000000000..6457f20ce2e --- /dev/null +++ b/data/38/51/1A/38511AD4D5A84A749725308AF02B1784.xml @@ -0,0 +1,87 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part C) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +370 +473 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Carex paniculata +Linnaeus + +, + +Centuria I Plantarum + +: 32. 1755 + + +. + + + +"Habitat in Europae australioribus uliginosis." RCN: 7071. + + + +Lectotype +(Egorova, +Sedges Russia +: 483. 1999): [icon] " + +Cyperus Alp. +longus inodorus panicula ferruginea minus sparsa + +" in Scheuchzer, Agrostographia Helv. Prodr.: 27, t. 8. 1708 (see p. 156). + + + + +Current name: + + +Carex paniculata + +L. + +( +Cyperaceae +). + + + + \ No newline at end of file diff --git a/data/38/51/37/3851376FFFC0B658F1F59019FE4796E8.xml b/data/38/51/37/3851376FFFC0B658F1F59019FE4796E8.xml new file mode 100644 index 00000000000..6abfc81a6b1 --- /dev/null +++ b/data/38/51/37/3851376FFFC0B658F1F59019FE4796E8.xml @@ -0,0 +1,75 @@ + + + +On the species composition of marine bivalves of the Sikhote-Alin Reserve (northern Primorye, Japan / East Sea) + + + +Author + +Kolpakov, E. V. + + + +Author + +Volvenko, I. Е. + +text + + +The Bulletin of the Russian Far East Malacological Society + + +2015 + +2015-12-24 + + +19 + + +31 +36 + + + +journal article +298416 +10.5281/zenodo.11087760 +32554a67-4e99-4f95-8abb-353b79a69dd1 +1560-8425 +11087760 + + + + + + +Panomya norvegica +(Spengler, 1973) + + + + + + +Рис. 2E, F + + +Fig. 2E, F + + +А р е а л. Широко распространенный бореально-арктический вид. ВстречаетсЯ в северной Атлантике, Северном Ледовитом океане и северной Пацифике [Скарлато, 1981; +Coan et al., 2000 +]. ДлЯ вод ПриморьЯ обычный вид, хотЯ и редок в сборах. +В +частности у берегов северного ПриморьЯ регистрировалсЯ всего в трех местах – у м. Титова, в Зал. Ольги и в б. Джигит [Колпаков, 2009; наШи данные; +Lutaenko, 1999 +]. + +М а т е р и а л. 04.1997 г., Японское море, северное Приморье, б. УдобнаЯ, Штормовые выбросы, сборЩик А. КостырЯ, 1 ЭкЗ. (рак.), № 16477/Bv-2239; 07.1997 г., Японское море, северное Приморье, б. УдобнаЯ, глубина 6–9 м, сборЩик А. КостырЯ, 1 ЭкЗ. (рак.), № 16471/Bv-2233 (рис. 2E, F). +Таким обраЗом, исследование коллекционных сборов ЗоомуЗеЯ УНМ ДВФУ поЗволило нам не только уточнить видовой состав морских двустворчатых моллюсков СихотЭ-Алинского биосферного Заповедника, но и дополнить имеюЩиесЯ в литературе сведениЯ о малакофауне северного ПриморьЯ. + + + \ No newline at end of file diff --git a/data/38/51/37/3851376FFFC6B658F1BF946AFEF79383.xml b/data/38/51/37/3851376FFFC6B658F1BF946AFEF79383.xml new file mode 100644 index 00000000000..c6baecd33d4 --- /dev/null +++ b/data/38/51/37/3851376FFFC6B658F1BF946AFEF79383.xml @@ -0,0 +1,166 @@ + + + +On the species composition of marine bivalves of the Sikhote-Alin Reserve (northern Primorye, Japan / East Sea) + + + +Author + +Kolpakov, E. V. + + + +Author + +Volvenko, I. Е. + +text + + +The Bulletin of the Russian Far East Malacological Society + + +2015 + +2015-12-24 + + +19 + + +31 +36 + + + +journal article +298416 +10.5281/zenodo.11087760 +32554a67-4e99-4f95-8abb-353b79a69dd1 +1560-8425 +11087760 + + + + + + +Zirfaea pilsbryi +Lowe, 1931 + + + + + + +А р е а л. Тихоокеанский Широко распространенный бореальный вид. НаселЯет Чукотское, Берингово, Охотское и Японское морЯ, воды тихоокеанского побережьЯ Канады, США и Мексики, а также тихоокеанскую сторону восточной Камчатки, Курильских и Командорских островов [Кафанов, 1991; Данилин, 2014; +Coan, Valentich-Scott, 2012 +; +Lutaenko, 2013 +]. +В +водах ПриморьЯ ранее укаЗывалсЯ только длЯ Зал. Петра Великого (южное Приморье) [Скарлато, 1981; +Lutaenko, Noseworthy, 2012 +]. + + + + +Рис. 2. A +, +B +. + +Modiolus +( +Modiolus +) +kurilensis +Bernard, 1983 + +: леваЯ створка снаружи (A), иЗнутри (B). Длина раковины 26.4 мм, высота – 47.3 мм; +C +, +D +. + +Gari +( +Gobraeus +) +kazusensis +(Yokoyama, 1922) + +: леваЯ створка снаружи (C), иЗнутри (D). Длина раковины 71.0 мм, высота – 39.9 мм. +E +, +F +. + +Panomya norvegica +(Spengler, 1973) + +: леваЯ створка снаружи (E), праваЯ створка иЗнутри (F). Длина раковины 70.8 мм, высота – 44.5 мм, толЩина – 36.7 мм. + + +Fig. 2. A +, +B +. + +Modiolus +( +Modiolus +) +kurilensis +Bernard, 1983 + +: left valve (A) outside, (B) inside. Shell length 26.4 mm, height – 47.3 mm. +C +, +D +. + +Gari +( +Gobraeus +) +kazusensis +(Yokoyama, 1922) + +: left valve (C) outside, (D) inside. Shell length 71.0 mm, height – 39.9 mm. +E +, +F +. + +Panomya norvegica +(Spengler, 1973) + +: left valve (E) outside, right valve (F) inside. Shell length 70.8 mm, height – 44.5 mm, thickness – 36.7 mm. + + + +М а т е р и а л. 07.1997 г., Японское море, северное Приморье, б. УдобнаЯ, глубина 6–9 м, сборЩик А. КостырЯ, 1 ЭкЗ. (ств.), № 16473/Bv-2235. + + + +З а м е ч а н и е. Створка передана длЯ иЗучениЯ д-ру G. Kennedy ( +USA +) и обратно в муЗей не воЗвраЩена [устное сообЩение К.А. Лутаенко]. На сохранивШейсЯ Этикетке надпись: +Pholadidae +, + +Zirfaea pilsbryi +Lowe, 1931 + +, Японское море (северное Приморье), б. БлагодатнаЯ +2 +, глубина 6–9 м, 07.1997 г., 1 ЭкЗ. (ств.), № XII 16473/Bv-2235, сборЩик А. КостырЯ, определение А. +В +. ЧерныШева. + + + + \ No newline at end of file diff --git a/data/38/51/37/3851376FFFC6B65EF128904BFC0991AA.xml b/data/38/51/37/3851376FFFC6B65EF128904BFC0991AA.xml new file mode 100644 index 00000000000..c1cccc8805f --- /dev/null +++ b/data/38/51/37/3851376FFFC6B65EF128904BFC0991AA.xml @@ -0,0 +1,86 @@ + + + +On the species composition of marine bivalves of the Sikhote-Alin Reserve (northern Primorye, Japan / East Sea) + + + +Author + +Kolpakov, E. V. + + + +Author + +Volvenko, I. Е. + +text + + +The Bulletin of the Russian Far East Malacological Society + + +2015 + +2015-12-24 + + +19 + + +31 +36 + + + +journal article +298416 +10.5281/zenodo.11087760 +32554a67-4e99-4f95-8abb-353b79a69dd1 +1560-8425 +11087760 + + + + + + +Modiolus +( +Modiolus +) +kurilensis +Bernard, 1983 + + + + + + +Рис. 2A, B + + +Fig. 2A, B + + +А р е а л. Тихоокеанский приаЗиатский субтропическо-бореальный вид. Обитает в Желтом и Японском морЯх, южной части Охотского морЯ, у тихоокеанского побережьЯ Японских и Курильских островов [Скарлато, 1981; +Bernard et al., 1993 +; +Lutaenko, 2013 +]. У берегов ПриморьЯ распространен ограниченно на север до б. РусскаЯ (45 +° +12′ с.Ш., наШи данные). Севернее у материкового побережьЯ Японского морЯ + +M. kurilensis + +встречаетсЯ еЩе только в Зал. Чихачева (Татарский пролив) [Мокиевский, 1960; Ромейко, 1993; Дуленина, 2013], т.е. имеет диЗЪюнктивный ареал. + + +М а т е р и а л. 04.1997 г., Японское море, северное Приморье, б. УдобнаЯ, Штормовые выбросы, сборЩик А. КостырЯ, 1 ЭкЗ. (ств.), № 16475/Bv-2237 (рис. 2А, +В +). + + + + \ No newline at end of file diff --git a/data/38/51/37/3851376FFFC6B65EF12F962BF96697F5.xml b/data/38/51/37/3851376FFFC6B65EF12F962BF96697F5.xml new file mode 100644 index 00000000000..cd648100698 --- /dev/null +++ b/data/38/51/37/3851376FFFC6B65EF12F962BF96697F5.xml @@ -0,0 +1,84 @@ + + + +On the species composition of marine bivalves of the Sikhote-Alin Reserve (northern Primorye, Japan / East Sea) + + + +Author + +Kolpakov, E. V. + + + +Author + +Volvenko, I. Е. + +text + + +The Bulletin of the Russian Far East Malacological Society + + +2015 + +2015-12-24 + + +19 + + +31 +36 + + + +journal article +298416 +10.5281/zenodo.11087760 +32554a67-4e99-4f95-8abb-353b79a69dd1 +1560-8425 +11087760 + + + + + + +Gari +( +Gobraeus +) +kazusensis +(Yokoyama, 1922) + + + + + + +Рис. 2C, D + + +Fig. 2C, D + + +А р е а л. Тихоокеанский приаЗиатский субтропическо-ниЗкобореальный вид. Распространен в Желтом, Бохайском и Японском морЯх [ +Qi et al., 1989 +; +Bernard et al., 1993 +; +Wang, 2004 +; +Lutaenko, 2013 +]. +В +водах ПриморьЯ был иЗвестен лиШь иЗ Зал. Петра Великого (южное Приморье) [ +Lutaenko, 2009 +]. + +М а т е р и а л. 07.1997 г., Японское море, северное Приморье, б. УдобнаЯ, глубина 6–9 м, сборЩик А. КостырЯ, 1 ЭкЗ. (ств.), № 16472/Bv-2234 (рис. 2C, D). + + + \ No newline at end of file diff --git a/data/38/51/48/385148939535A2598B111E8AA5ED39A4.xml b/data/38/51/48/385148939535A2598B111E8AA5ED39A4.xml new file mode 100644 index 00000000000..0dbe56b57a7 --- /dev/null +++ b/data/38/51/48/385148939535A2598B111E8AA5ED39A4.xml @@ -0,0 +1,58 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Ostrea striatula +[ +spec. nov. +] + + + + +O. testa radiis 16 obliteratis transverse membranaceo striatis, margine integerrimo. +M. L. U. + + + + +Habitat in +O. Indico. + + + + +Valvula convexior paulo magis gibba, quam planior +; +color +intus flavescens radiorum interstitiis albis. + + + + \ No newline at end of file diff --git a/data/38/51/8E/38518E462A0760EEAD632E5E2662C80F.xml b/data/38/51/8E/38518E462A0760EEAD632E5E2662C80F.xml new file mode 100644 index 00000000000..5d35e2e5ad3 --- /dev/null +++ b/data/38/51/8E/38518E462A0760EEAD632E5E2662C80F.xml @@ -0,0 +1,120 @@ + + + +Updated catalogue and taxonomic notes on the Old-World scorpion genus Buthus Leach, 1815 (Scorpiones, Buthidae) + + + +Author + +Sousa, Pedro + + + +Author + +Arnedo, Miquel A. + + + +Author + +Harris, D. James + +text + + +ZooKeys + + +2017 + +686 + + +15 +84 + + + + +http://dx.doi.org/10.3897/zookeys.686.12206 + +journal article +http://dx.doi.org/10.3897/zookeys.686.12206 +1313-2970-686-15 +976E23A1CFC74CB381705B59452825A6 + + + + +32. + +Buthus lienhardi +Lourenco +, 2003 + + + + + +Buthus lienhardi +: + +Lourenco +2003 + +: 899-902, fig. 62-69; +Stockmann and Ythier 2010 +: 362-363; +Touloun and Boumezzough 2011a +: 186; +Touloun 2012 +: 37, fig.5C; + +Aboumaad +et al. 2014 + +: 6. + + +Buthus occitanus tunetatus Lepineyi +: Vachon 1949: 353-359, fig. 393-400; +Vachon 1952a +: 281-286, fig. 393-400; + + +Buthus occitanus tunetatus lepineyi +: +Malhomme 1954 +: 29-30; Le Corroller 1967: 63; +Perez +1974: 22; +Touloun et al. 1999 +: 1; +Touloun et al. 2001 +: 2; +Touloun 2012 +: 37. + + +Buthus occitanus tunetatus +(MIS): +Touloun 2012 +: 104, 108. + + + +Type material. +1 M holotype (MHNG), Oukaimeden (approx. 31.201°, -7.861°), Marrakech, Morocco. Paratypes: 1 F, 2 juv. (MHNG), same locality. + + +Distribution. +the species is known from a wide range across the High-Atlas Mountains. + + +Remarks. +Vachon (1949) infrasubspecific name is not available as explained previously. + + + \ No newline at end of file diff --git a/data/38/51/D5/3851D53CA5CFC2891CD8AAC52F730A3F.xml b/data/38/51/D5/3851D53CA5CFC2891CD8AAC52F730A3F.xml new file mode 100644 index 00000000000..40c12cf6320 --- /dev/null +++ b/data/38/51/D5/3851D53CA5CFC2891CD8AAC52F730A3F.xml @@ -0,0 +1,104 @@ + + + +Annotated type catalogue of the Bulimulidae (Mollusca, Gastropoda, Orthalicoidea) in the Natural History Museum, London + + + +Author + +Breure, Abraham S. H. +Naturalis Biodiversity Center, P. O. Box 9517, Leiden, the Netherlands +bbreure@xs4all.nl + + + +Author + +Ablett, Jonathan D. +Natural History Museum, Division of Higher Invertebrates, London, SW 7 5 BD, UK + +text + + +ZooKeys + + +2014 + +2014-03-21 + + +392 + + +1 +367 + + + + +http://dx.doi.org/10.3897/zookeys.392.6328 + +journal article +http://dx.doi.org/10.3897/zookeys.392.6328 +1313-2970-392-1 +FFCF5A59FFB1FF93FFF10B43FFAFFFF5 +578044 + + + + +Bulimus andicola Pfeiffer, 1847 +Figs 23A +, L4iv + + + + +Bulimus andicola +Pfeiffer 1847 +: 115; +Reeve 1848 [1848-1850] +: pl. 55 fig. 364; +Breure 1979 +: 117 (lectotype designation). + + +Bulimulus (Lissoacme) andicola +; +Pilsbry 1896 [1895-1896] +: 166, pl. 50 fig. 46. + + + +Type locality. +"Columbian Andes". + + +Label. + +"Andes of Columbia", taxon label in +Pfeiffer's +handwriting. M.C. label style IV, V. + + + +Dimensions. +"Long. 24, diam. 11 mill."; figured specimen herein H 24.1, D 10.7, W 7.1. + + +Type material. +NHMUK 1975315, lectotype; NHMUK 1975316, two paralectotypes (Cuming coll.). + + +Current systematic position. + + +Drymaeus (Mesembrinus) andicola + +(Pfeiffer, 1847). + + + + \ No newline at end of file diff --git a/data/38/52/02/385202E0C7B45AE284D54FD13B4F4CDF.xml b/data/38/52/02/385202E0C7B45AE284D54FD13B4F4CDF.xml new file mode 100644 index 00000000000..b239bc1cfaf --- /dev/null +++ b/data/38/52/02/385202E0C7B45AE284D54FD13B4F4CDF.xml @@ -0,0 +1,135 @@ + + + +Taxonomic review of the Cataglyphis livida complex (Hymenoptera, Formicidae), with a description of a new species from Iran + + + +Author + +Salata, Sebastian +https://orcid.org/0000-0003-0811-2309 +Department of Biodiversity and Evolutionary Taxonomy, University of Wroclaw, Przybyszewskiego 65, 51 - 148, Wroclaw, Poland & California Academy of Sciences, 55 Music Concourse Dr, San Francisco, 94118, CA, USA +sdsalata@gmail.com + + + +Author + +Kiyani, Haniyeh +Department of Plant Protection, Faculty of Agriculture, Shiraz University, Shiraz, Iran + + + +Author + +Minaei, Kambiz +Department of Plant Protection, Faculty of Agriculture, Shiraz University, Shiraz, Iran + + + +Author + +Borowiec, Lech +https://orcid.org/0000-0001-5668-6855 +Department of Biodiversity and Evolutionary Taxonomy, University of Wroclaw, Przybyszewskiego 65, 51 - 148, Wroclaw, Poland + +text + + +ZooKeys + + +2021 + +2021-01-13 + + +1010 + + +117 +131 + + + + +http://dx.doi.org/10.3897/zookeys.1010.58348 + +journal article +http://dx.doi.org/10.3897/zookeys.1010.58348 +1313-2970-1010-117 +FA1B6869B8C74BC1B7DCE3016C5F6CB9 +E04C6694C9155258BB639EFE8FBF3FD9 + + + + +Cataglyphis lutea Pisarski, 1967 +stat. rev. + + + + +Cataglyphis livida subsp. lutea +Pisarski, 1967: 418 [first available use of +Myrmecocystus albicans viaticoides +Cataglyphis lutea +Emery, 1906: 53]. + + +Myrmecocystus albicans viaticoides +Junior synonym of +Cataglyphis livida +: Radchenko, 1997: 428. + + +Myrmecocystus albicans viaticoides +Syntype worker, Shiraz, Iran (MSNG) [Syntype worker images examined, AntWeb, CASENT0905718, photographs by Will Ericson, available on AntWeb.org]. + + + +Diagnosis. +Whole body yellow, only gaster sometimes with indistinctly infuscated apex; body never with a layer of silvery hair. + + +Distribution. +Species known from Arabian Peninsula east to Afghanistan. + + +Note. + + +Cataglyphis lutea + +was described from Shiraz, Fars Province in Iran as an unavailable quadrinominal name ( +Emery 1906 +), later validated by +Pisarski (1967) +as a subspecies of + +C. livida + +, and finally considered as its junior synonym ( +Radchenko 1997 +). A study on type specimen revealed that + +C. lutea + +distinctly differs from + +C. livida + +in lack of a layer of silvery hair on mesosoma, and its distribution does not overlap with confirmed records of + +C. livida + +. Thus, we decided to raise it to the species status. AntCat resources indicated that, except type locality, + +C. lutea + +is also known from Aran va Bidgol, Maranjab, Iran (CDA000106) and Saudi Arabia (CASENT0906455). + + + + \ No newline at end of file diff --git a/data/38/52/24/3852248B0E32842184F82CF476CEB490.xml b/data/38/52/24/3852248B0E32842184F82CF476CEB490.xml new file mode 100644 index 00000000000..c910dcc78a2 --- /dev/null +++ b/data/38/52/24/3852248B0E32842184F82CF476CEB490.xml @@ -0,0 +1,128 @@ + + + +Generic placement of the Neotropical species of " Phragmatobia " (Erebidae, Arctiinae), with a remarkable matrivorous species from the Peruvian Andes + + + +Author + +Schmidt, B. Christian + + + +Author + +Freina, Josef J. De + +text + + +ZooKeys + + +2011 + +149 + + +69 +88 + + + + +http://dx.doi.org/10.3897/zookeys.149.2382 + +journal article +http://dx.doi.org/10.3897/zookeys.149.2382 +1313-2970-149-69 + + + + +Patagobia thursbyi (Rothschild) +comb. n. + + + + +Turuptiana thursbyi +Rothschild 1910 +: 176, comb. n. Five male syntypes (BMNH). Type locality: [ +Argentina +], Patagonia, Chubut, Valley de Lago Blanco. + + +Phragmatobia thursbyi pluto +Toulgoet +, 1987: 241, syn. n. + + + +Type material. +Male holotype (ZMUC). Type locality: Argentina, Rio Negro, San Carlos de Bariloche, Colonia Suiza, 810 m. + + +Diagnosis. + +The taxon pluto +Toulgoet +has been treated as a subspecies distinct from nominate thursbyi based on the nearly unicolourous forewing, resulting from the confluence of the transverse bands. Genitalic structure of both taxa is identical ( + +Toulgoet +1987 + +). Examination of series of specimens from a single locality (Fig. 4b-d) shows that there is considerable variation in the extent of forewing banding, and also in the hindwing ground colour. We therefore treat pluto as a synonym of nominate +Patagobia thursbyi +. + + + +Remarks. + +No detailed habitat information is available for +Patagobia thursbyi +, but locality information shows that it occurs from about 800 m elevation at the southern range edge (46°S) to 2700 m farther north (33°S), corresponding to temperate montane woodlands and grasslands of Patagonia. This region is well known for its high level of endemic species, and circumantarctic tree genera such as +Araucaria +Juss. and + +Nothofagus + +Blume ( +World Wildlife Fund 2001 +). Examined specimens and literature records (Fig. 18) are as follows Chile - Malleco Prov.: Cordillera las Raices, Lonquimay, 1050 m (CNC, ZSM); La Fusta, 1200 m (CNC, ZSM); Cordillera Lonquimay, Icalama 1000 m (AMNH, ZSM); Termas de Rio Blanco ( +Ruiz 1989 +, ZSM); Cautin region ( +Ruiz 1989 +); Nuble Prov.: Chillan, ( +Ruiz 1989 +); Santiago: Cantillana [highlands], [Laguna de] Aculeo ( + +Toulgoet +1987 + +). Argentina - Chubut Prov.: Valle del Lago Blanco (BMNH, ZSM); Neuquen Prov.: Pampa Tromen, Huayilon ( +Ruiz 1989 +, ZSM); San Martin de los Andes (ZSM); +Alumine +, 1200 m ( + +Toulgoet +1987 + +); Rio Negro Prov.: San Carlos de Bariloche, Colonia Suisa, 810 m ( + +Toulgoet +1987 + +, ZSM); Paso Flores (ZSM); Mendoza region, 2750 m ( + +Toulgoet +1987 + +). + + + + \ No newline at end of file diff --git a/data/38/52/49/3852490E21820EB6FA59901C0CEED113.xml b/data/38/52/49/3852490E21820EB6FA59901C0CEED113.xml new file mode 100644 index 00000000000..305caf2a491 --- /dev/null +++ b/data/38/52/49/3852490E21820EB6FA59901C0CEED113.xml @@ -0,0 +1,90 @@ + + + +Revision of the myrmicine ants of the Adelomyrmex genus-group (Hymenoptera: Formicidae). + + + +Author + +Fernández, F. + +text + + +Zootaxa + + +2003 + +361 + + +1 +52 + + + + +http://www.mapress.com/zootaxa/2003/zt00361.pdf + +journal article +20236 +10.5281/zenodo.32035 + + + + + +Adelomyrmex cristiani +Fernandez + +NEW SPECIES +(Figs. 36, 75) + + + +Worker measurements. Holotype. HL 0.50 HW 0.44 SL 0.23 EL 0.04 WL 0.39 GL 0.60 TL 1.87 CI 88 SI 52. + + +Worker diagnosis: Mandibles with 5 teeth decreasing in size from the apical teeth. Clypeal median seta short. Dorsum of clypeal plate with two curved ridges prolongued into frontal carinae. Lateral clypeal teeth very small. The last antennal flagellomere much broader than long, their length more or less as flagellomeres 2 to 10. Eyes small, with approximately 6 ommatidia. Hypostomal tooth very small, but visible. Mesosomal dorsum evenly arched, metanotal groove broad and shallow. Propodeum with sharp angulation instead of spines. Propodeal lobes slightly angulated. Petiole high in profile, more high than postpetiole, with anterior face evenly meeting the rounded dorsal face, then to inclined posterior face. Head and promesonotum longitudinally rugulose, rugulae on mesonotum more coarse; short dorsal propodeal face irregularly rugulated; propodeal declivity transversely rugulated between propodeal spines. Gaster smooth and shining with numerous dark punctures. Few long hairs on clypeus, frontal carinae and occipital borders; several suberect hairs on mesosomal dorsum, several long and flexuous hairs on petiole, postpetiole and gaster. Body light brown, legs and antennae paler. +Queen and worker: Unknown. + + + + +Holotype +worker: +COLOMBIA +: + +Cordillera Occidental, transecto +Tatama +, 1650m + +, +1983 +, +Th. van der Hammen et al. +, +TAT 205 +. Deposited in +ICN +. + + + + +Comments. This is one of the smaller species of the genus. It can be recognized by short clypeal setae, small and poorly-faceted eyes, evenly curved mesosoma, broad propodeal angulation, petiole higher than postpetiole, and first gastric tergite with several dark punctures. + + + +This species is named in honor of Dr. +Cristian +T. Samper K., general director of Instituto Humboldt from its creation in 1995 through 2001, for his friendship and strong support of insect surveys and collection in the Institute. Many of the goals in entomological research here have been set with the assistance and unfailing support of +Cristian +. + + + + \ No newline at end of file diff --git a/data/38/52/D5/3852D52EFFC03B28FF6EF932B3F2A6F1.xml b/data/38/52/D5/3852D52EFFC03B28FF6EF932B3F2A6F1.xml new file mode 100644 index 00000000000..db0a484b34e --- /dev/null +++ b/data/38/52/D5/3852D52EFFC03B28FF6EF932B3F2A6F1.xml @@ -0,0 +1,265 @@ + + + +New species and taxonomic notes of scaly crickets (Orthoptera: Mogoplistidae Mogoplistinae) from Borneo + + + +Author + +Tan, Ming Kai +Institut de Systématique, Evolution et Biodiversité (ISYEB), Muséum national d’Histoire naturelle, CNRS, SU, EPHE, UA, 57 rue Cuvier, CP 50, 75231 Paris Cedex 05, France. + + + +Author + +Japir, Razy +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Razy. Japir @ sabah. gov. my + + + +Author + +Chung, Arthur Y. C. +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Arthur. Chung @ sabah. gov. my; https: // orcid / org / 0000 - 0002 - 9529 - 4114 +hung@sabah.gov.my + + + +Author + +Wahab, Rodzay Bin Haji Abdul +Institute for Biodiversity and Environmental Research, Universiti Brunei Darussalam, Jalan Universiti, BE 1410, Brunei Darussalam. rodzay. wahab @ ubd. edu. bn; https: // orcid / org / 0000 - 0002 - 2151 - 7709 +rodzay.wahab@ubd.edu.bn + +text + + +Zootaxa + + +2021 + +2021-10-07 + + +5048 + + +3 + + +407 +421 + + + +journal article +4053 +10.11646/zootaxa.5048.3.6 +6456e942-b39b-4899-b2a9-f4deecde44d9 +1175-5326 +5556495 +AB9AF652-CA1B-4BB5-927F-BC3A12BA73D9 + + + + + + + +Ectatoderus nigrofasciatus +Tan & Wahab + +, +new species + + + + + + +( +Figs. 5–7 +) + + + + +Material examined. + + +Holotype + +, male ( +BRU +.19.70), +BRUNEI DARUSSALAM +, +Belait District +, +Jalan Labi +near +Andulau Forest Reserve +, +N4.63354 +, +E114.51047 +, 76.6±5.0 m.a.s.l., on rattan foliage, + +7 July 2019 + +, 2042h, coll. +M. K. Tan +( +UBDM +). + + + + + +Diagnosis. +The new species is characterised by the scapus being dorsally black but ventrally and laterally brown, and the antennae being wholly black; the head has a distinct black band behind eyes; and the male phallic complex has the medial valve elongated, not curved to a spiral, sinuous both dorso-ventrally and laterally and with the ventro-external sclerite of the lateral valve being elongated, in basal third broader, and tapering into a narrow lamella with subacute apex. + + +The new species is closest in distribution to + +E. angusticollis +Chopard, 1969 + +from +Singapore +. In both species the pronotum is more strongly widening apicad, and fore and middle tibiae are provided with black dorsal stripes. The new species differs by the scapus and antennae being black instead of testaceous, by the head being provided with a distinct black band behind eyes and by the male phallic complex having the medial valve not curved to a spiral. + + +The new species is most similar to + +E. argentatus +Ingrisch, 2006 + +from +Thailand +having the pronotum strongly widening apicad and the frons dark; it differs by the darked scapus and basal antennal segments instead of being yellow brown, by the male phallic complex which is more elongated and having the medial valve sinuous rather than curving upward (basally) and by the shape of the apical sclerotization of the medial valve. + + + +FIGURE 4. + +Cycloptiloides bimaculata +Tan, Japir & Chung + +, + +sp. nov. + +male holotype: head (A) and inner tympanum (B) in lateral view; male abdominal apex in dorsal (C in ethanol, D from live photograph), lateral (E) and ventral (F) views. Scale bars: 1 mm (all except B), 0.5 mm (B). + + + + +FIGURE 5. + +Ectatoderus nigrofasciatus +Tan & Wahab + +, + +sp. nov. + +male holotype on a palm/ rattan leaf in Belait. + + + +This new species also differs from + +E. samui +Ingrisch, 2006 + +from +Thailand +by the pronotum being more strongly widening apicad and by the male phallic complex having the medial valve not curved to a spiral; from + +E. marginatus +Bey-Bienko, 1966 + +from Lesser Sunda Islands it differs by the pronotum being more strongly widening apicad. + + + + +Etymology. +The species name refers to the black band posterior of eyes and the black scapus (dorsally only) and antennae; nigro = black in Latin, fascia = band in Latin. + + + + +Description. +Habitus of male as shown in +Fig. 5 +. Dorsum of head flattened ( +Figs. 6A, 6B +). Frontal rostrum 1.3 times wider than scapus ( +Fig. 6A +). Maxillary palps with apical (= fifth) and subapical (= fourth) segments of subequal length, third segment longer than apical and subapical segments; apical segment triangular and widened apically ( +Fig. 6B +). Pronotum about 1.7 times longer than wide with anterior dorsal margin narrow and straight; lateral margin widening posteriorly; strongly produced posteriorly and covering near-entirely tegmen; posterior margin convex. Fore tibia with internal tympanum small and oval; without external tympanum. Hind femur 1.1 times longer than hind tibia; hind tibia 4.4 times longer than hind metatarsus. + + +Male. Supra-anal plate with last abdominal tergite and epiproct distinctly separated by a transverse suture; last abdominal tergite transverse, with hind margin emarginate; supra-anal plate less transverse than last abdominal tergite, flattened, with fewer setae, apex rounded ( +Fig. 6E +). Genitalia as in +Fig. 7 +. Epiphallus elongated and membranous. Medial valve elongated, not curved to a spiral, sinuous both dorso-ventrally and laterally. Lateral valves weakly sclerotised, forming stout and truncated lobes at apex. Ventro-external sclerite of lateral valve elongate, basal third broader, tapering into a narrow lamella with subacute apex. + +Female. Unknown. + +Colouration. Head dorsum light brown, with white stripe running along lateral margin from posterior end, along inner margin of eyes to frontal rostrum ( +Figs. 6B, 6D +). Scapus dorsally black, otherwise brown ( +Figs. 6A, 6D +); basal antennal segments black, thereafter brown with some segments black ( +Figs. 6A, 6D +). Frons and mouthparts dark coloured ( +Fig. 6C +). Maxillary and labial palps yellow brown ( +Figs. 6B, 6C +). Lateral parts of head, including genae, light brown; with a black horizontal band behind eyes. Pronotal dorsal disc brown, apical margin with white scales. Pronotal lateral lobes also with white scales and with brown margins ( +Fig. 6D +). Tegmen mostly infumated white, but infumated grey at apical area of lateral field ( +Fig. 6D +). Femur generally pale brown to brown. Fore and middle tibiae dorsally black, otherwise brown. Tarsi with basal segment brown, with middle and apical segments black. Hind femur generally brown with knee dark. Hind tibia brown, dorsally pale yellow. Abdomen with tergites black covered with greyish brown scales; sternites black with whitish scales especially on those nearer to thorax. Abdominal apex black; last abdominal tergite back with brown setae along posterior margin ( +Fig. 6E +). Cercus brown. + + + +FIGURE 6. + +Ectatoderus nigrofasciatus +Tan & Wahab + +, + +sp. nov. + +male: head and pronotum in dorsal (A) and lateral (D) views, head in lateral (B) and anterior (C) views; abdominal apex in dorsal view (E). Scale bars: 1 mm. + + + +Measurements (in mm). +Holotype +BL = 7.6; FRW = 0.28; SW = 0.22; EW = 0.26; PL = 3.9; PW = 2.2; TL = 2.3; HFL = 4.3; HFW = 1.3; HTL = 4.0; HML = 0.9. + + + + +Distribution. +Borneo ( +Brunei Darussalam +) + + + + \ No newline at end of file diff --git a/data/38/52/D5/3852D52EFFC43B20FF6EFA22B539A172.xml b/data/38/52/D5/3852D52EFFC43B20FF6EFA22B539A172.xml new file mode 100644 index 00000000000..8dcfe7e9df0 --- /dev/null +++ b/data/38/52/D5/3852D52EFFC43B20FF6EFA22B539A172.xml @@ -0,0 +1,107 @@ + + + +New species and taxonomic notes of scaly crickets (Orthoptera: Mogoplistidae Mogoplistinae) from Borneo + + + +Author + +Tan, Ming Kai +Institut de Systématique, Evolution et Biodiversité (ISYEB), Muséum national d’Histoire naturelle, CNRS, SU, EPHE, UA, 57 rue Cuvier, CP 50, 75231 Paris Cedex 05, France. + + + +Author + +Japir, Razy +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Razy. Japir @ sabah. gov. my + + + +Author + +Chung, Arthur Y. C. +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Arthur. Chung @ sabah. gov. my; https: // orcid / org / 0000 - 0002 - 9529 - 4114 +hung@sabah.gov.my + + + +Author + +Wahab, Rodzay Bin Haji Abdul +Institute for Biodiversity and Environmental Research, Universiti Brunei Darussalam, Jalan Universiti, BE 1410, Brunei Darussalam. rodzay. wahab @ ubd. edu. bn; https: // orcid / org / 0000 - 0002 - 2151 - 7709 +rodzay.wahab@ubd.edu.bn + +text + + +Zootaxa + + +2021 + +2021-10-07 + + +5048 + + +3 + + +407 +421 + + + +journal article +4053 +10.11646/zootaxa.5048.3.6 +6456e942-b39b-4899-b2a9-f4deecde44d9 +1175-5326 +5556495 +AB9AF652-CA1B-4BB5-927F-BC3A12BA73D9 + + + + + + +Genus + +Apterornebius +Ingrisch, 2006 + + + + + + + +Remarks. +Since its description, the genus consists of two species, + +A. chong +Ingrisch, 2006 + +from +Thailand +and +Singapore +( +Ingrisch, 2006 +; +Tan, 2012 +, +2017 +) and + +A. kinabalu +Ingrisch, 2006 + +from Borneo. + + + + \ No newline at end of file diff --git a/data/38/52/D5/3852D52EFFC43B23FF6EF94AB212A63E.xml b/data/38/52/D5/3852D52EFFC43B23FF6EF94AB212A63E.xml new file mode 100644 index 00000000000..c0f2fddd897 --- /dev/null +++ b/data/38/52/D5/3852D52EFFC43B23FF6EF94AB212A63E.xml @@ -0,0 +1,155 @@ + + + +New species and taxonomic notes of scaly crickets (Orthoptera: Mogoplistidae Mogoplistinae) from Borneo + + + +Author + +Tan, Ming Kai +Institut de Systématique, Evolution et Biodiversité (ISYEB), Muséum national d’Histoire naturelle, CNRS, SU, EPHE, UA, 57 rue Cuvier, CP 50, 75231 Paris Cedex 05, France. + + + +Author + +Japir, Razy +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Razy. Japir @ sabah. gov. my + + + +Author + +Chung, Arthur Y. C. +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Arthur. Chung @ sabah. gov. my; https: // orcid / org / 0000 - 0002 - 9529 - 4114 +hung@sabah.gov.my + + + +Author + +Wahab, Rodzay Bin Haji Abdul +Institute for Biodiversity and Environmental Research, Universiti Brunei Darussalam, Jalan Universiti, BE 1410, Brunei Darussalam. rodzay. wahab @ ubd. edu. bn; https: // orcid / org / 0000 - 0002 - 2151 - 7709 +rodzay.wahab@ubd.edu.bn + +text + + +Zootaxa + + +2021 + +2021-10-07 + + +5048 + + +3 + + +407 +421 + + + +journal article +4053 +10.11646/zootaxa.5048.3.6 +6456e942-b39b-4899-b2a9-f4deecde44d9 +1175-5326 +5556495 +AB9AF652-CA1B-4BB5-927F-BC3A12BA73D9 + + + + + + + +Apterornebius kinabalu +Ingrisch, 2006 + + + + + + + +( +Fig. 1 +) + + + + + + + +Apterornebius kinabalu +Ingrisch, 2006: 165 + + + + + + + +Material examined. +1 male +(SDK.19.103) and + +1 female +(SDK.19.104), EAST +MALAYSIA +, +Sandakan +, +Kabili Sepilok Forest Reserve +, +N5.87084 +, +E117.93764 +, 98.7± + +6.1 m + +.a.s.l., mating on foliage, + +3 October 2019 + +, 2058h, coll. +M. K. Tan +& +J. L. Yukang +( +FRC +) + +. + + + + +Distribution. +Borneo ( +Sabah +: Sorinsim on +Kinabalu, Sepilok +in Sandakan) + + + + +Remarks. +The specimens reported agree with the original description by +Ingrisch (2006) +in general habitus, maxillary palps, male abdominal apex, male phallic complex and female ovipositor ( +Fig. 1 +). The locality Sepilok is a new record for this species that was described and previously known only from Kinabalu. While Kinabalu is a mountainous terrain, Sandakan has a lower and flatter terrain. + + + + \ No newline at end of file diff --git a/data/38/52/D5/3852D52EFFC63B22FF6EF987B25DA0EE.xml b/data/38/52/D5/3852D52EFFC63B22FF6EF987B25DA0EE.xml new file mode 100644 index 00000000000..5ef5c5da014 --- /dev/null +++ b/data/38/52/D5/3852D52EFFC63B22FF6EF987B25DA0EE.xml @@ -0,0 +1,145 @@ + + + +New species and taxonomic notes of scaly crickets (Orthoptera: Mogoplistidae Mogoplistinae) from Borneo + + + +Author + +Tan, Ming Kai +Institut de Systématique, Evolution et Biodiversité (ISYEB), Muséum national d’Histoire naturelle, CNRS, SU, EPHE, UA, 57 rue Cuvier, CP 50, 75231 Paris Cedex 05, France. + + + +Author + +Japir, Razy +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Razy. Japir @ sabah. gov. my + + + +Author + +Chung, Arthur Y. C. +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Arthur. Chung @ sabah. gov. my; https: // orcid / org / 0000 - 0002 - 9529 - 4114 +hung@sabah.gov.my + + + +Author + +Wahab, Rodzay Bin Haji Abdul +Institute for Biodiversity and Environmental Research, Universiti Brunei Darussalam, Jalan Universiti, BE 1410, Brunei Darussalam. rodzay. wahab @ ubd. edu. bn; https: // orcid / org / 0000 - 0002 - 2151 - 7709 +rodzay.wahab@ubd.edu.bn + +text + + +Zootaxa + + +2021 + +2021-10-07 + + +5048 + + +3 + + +407 +421 + + + +journal article +4053 +10.11646/zootaxa.5048.3.6 +6456e942-b39b-4899-b2a9-f4deecde44d9 +1175-5326 +5556495 +AB9AF652-CA1B-4BB5-927F-BC3A12BA73D9 + + + + + + +Genus + +Ectatoderus +Guérin-Méneville, 1847 + + + + + + +List of Southeast Asian species: + + + + + + +Ectatoderus angusticollis +Chopard, 1969 + +from +Singapore + + + +Ectatoderus apterus +(Chopard, 1925) + +from Java + + + +Ectatoderus argentatus +Ingrisch, 2006 + +from +Thailand + + + +Ectatoderus marginatus +Bey-Bienko, 1966 + +from Lesser Sunda Islands + + + +Ectatoderus pallidegeniculatus +Brunner von Wattenwyl, 1893 + +from +Myanmar +[probably + +Micrornebius + +] + +Ectatoderus samui +Ingrisch, 2006 + +from +Thailand + + + +Ectatoderus sordidus +(Walker, 1869) + +from New +Guinea + + + + \ No newline at end of file diff --git a/data/38/52/D5/3852D52EFFC63B22FF6EFF7FB250A13D.xml b/data/38/52/D5/3852D52EFFC63B22FF6EFF7FB250A13D.xml new file mode 100644 index 00000000000..4578290b35a --- /dev/null +++ b/data/38/52/D5/3852D52EFFC63B22FF6EFF7FB250A13D.xml @@ -0,0 +1,301 @@ + + + +New species and taxonomic notes of scaly crickets (Orthoptera: Mogoplistidae Mogoplistinae) from Borneo + + + +Author + +Tan, Ming Kai +Institut de Systématique, Evolution et Biodiversité (ISYEB), Muséum national d’Histoire naturelle, CNRS, SU, EPHE, UA, 57 rue Cuvier, CP 50, 75231 Paris Cedex 05, France. + + + +Author + +Japir, Razy +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Razy. Japir @ sabah. gov. my + + + +Author + +Chung, Arthur Y. C. +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Arthur. Chung @ sabah. gov. my; https: // orcid / org / 0000 - 0002 - 9529 - 4114 +hung@sabah.gov.my + + + +Author + +Wahab, Rodzay Bin Haji Abdul +Institute for Biodiversity and Environmental Research, Universiti Brunei Darussalam, Jalan Universiti, BE 1410, Brunei Darussalam. rodzay. wahab @ ubd. edu. bn; https: // orcid / org / 0000 - 0002 - 2151 - 7709 +rodzay.wahab@ubd.edu.bn + +text + + +Zootaxa + + +2021 + +2021-10-07 + + +5048 + + +3 + + +407 +421 + + + +journal article +4053 +10.11646/zootaxa.5048.3.6 +6456e942-b39b-4899-b2a9-f4deecde44d9 +1175-5326 +5556495 +AB9AF652-CA1B-4BB5-927F-BC3A12BA73D9 + + + + + + + +Cycloptiloides bimaculata +Tan, Japir & Chung + +, +new species + + + + + + +( +Figs. 2–4 +) + + + + + + +Micrornebius incertus +( +Ingrisch, 1998 +) + +— + +Ingrisch, 1998: 232 + +[one of the females (not a +type +) erroneous described under + +Derectaotus incertus + +] + + + + + +Cycloptiloides +sp. 1 + +— + +Ingrisch, 2006: 185 + + + + + + +Material examined. + + +Holotype + +, male (SDK.19.20), EAST +MALAYSIA +, +Sabah +, +Sandakan +, +Sepilok +, +Rainforest Discovery Centre +, +N5.87580 +, +E117.94299 +, 39.1± + +5.4 m + +.a.s.l., leaf litter, + +9 January 2019 + +, 1911h, coll. +M. K. Tan +, R. +Japir, M +. +Binti, J. L +. Yukang ( +FRC +). + + + + +Paratypes + +, +2 females +: + +1 female +(SDK.19.19), same locality, +N5.87356 +, +E117.94172 +, 49.1± + +5.2 m + +.a.s.l., leaf litter, + +9 January 2019 + +, 1105h, coll. +M. K. Tan +, R. +Japir, M +. +Binti, J. L +. Yukang + +; + +1 female +(SDK.19.35), same locality, +N5.87553 +, +E117.94116 +, 33.4± + +4.9 m + +.a.s.l., + +9 January 2019 + +, 2040h, coll. +M. K. Tan +, R. +Japir, M +. +Binti, J. L +. Yukang (all +FRC +) + +. + + + + +Remarks. +Ingrisch (2006) +described the female of this species as + +Cycloptiloides +sp. 1 + +without providing a species name. Here, we provide a formal name, assign a male +holotype +and describe the male. + + + + +Diagnosis. +The male differs from congeners by the supra-anal plate trapezoidal in shape with apical margin broadly rounded, with dark scales and yellow brown setae laterally and shiny pale in the middle (forming two spots). The female differs from congeners by shorter maxillary palps and ovipositor and more transverse supra-anal plate ( +Ingrisch, 2006 +). + + + + +Etymology. +The species name refers to the two spots in the middle of the supra-anal plate; bi = two in Latin, maculata = spotted in Latin. + + + + +Description. +Habitus of male as shown in +Figs. 2 +, +3 +. Dorsum of head flattened ( +Fig. 3A +). Frontal rostrum 1.2 times wider than scapus. Maxillary palps with apical (= fifth) a little longer than subapical (= fourth) and third segments, subapical and third segments subequal lengths; apical segment little widened ( +Fig. 4A +). Pronotum about 1.5 times longer than wide with anterior dorsal margin distinctly concave; lateral margin subparallel in anterior half and faintly widening posteriorly; covering tegmen entirely; posterior margin convex. Fore tibia with internal tympanum large and elongate oval ( +Fig. 4B +); without external tympanum. Hind femur 1.4 times longer than hind tibia; hind tibia 2.1 times longer than hind metatarsus. + + +Male. Supra-anal plate trapezoidal with apical margin broadly rounded, with setae at lateral parts ( +Figs. 4C, 4D +). Subgenital plate trapezoidal, posterior margin slightly convex ( +Fig. 4F +). Epiphallus and phallic complex hyaline ( +Fig. 4E +). + + +Female. Already sufficiently described in +Ingrisch (2006) +. Our female specimens from Sandakan agree with the description. + + +Colouration. General colouration similar to female described in +Ingrisch (2006) +. Male supra-anal plate with dark scales laterally, middle shining pale coloured (forming two spots) ( +Figs. 4C, 4D +). Cercus (both male and females) with brown scales. + + +Measurements (in mm). +Holotype +BL = 3.9; FRW = 0.27; SW = 0.14; EW = 0.14; PL = 1.9; PW = 1.3; HFL = 2.5; HFW = 0.9; HTL = 1.8; HML = 0.8. + + + + +Distribution. +Borneo ( +Sabah +: +Kinabalu, Sandakan +) + + + + \ No newline at end of file diff --git a/data/38/52/D5/3852D52EFFCC3B28FF6EFC04B452A3FD.xml b/data/38/52/D5/3852D52EFFCC3B28FF6EFC04B452A3FD.xml new file mode 100644 index 00000000000..56e00fa4db4 --- /dev/null +++ b/data/38/52/D5/3852D52EFFCC3B28FF6EFC04B452A3FD.xml @@ -0,0 +1,124 @@ + + + +New species and taxonomic notes of scaly crickets (Orthoptera: Mogoplistidae Mogoplistinae) from Borneo + + + +Author + +Tan, Ming Kai +Institut de Systématique, Evolution et Biodiversité (ISYEB), Muséum national d’Histoire naturelle, CNRS, SU, EPHE, UA, 57 rue Cuvier, CP 50, 75231 Paris Cedex 05, France. + + + +Author + +Japir, Razy +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Razy. Japir @ sabah. gov. my + + + +Author + +Chung, Arthur Y. C. +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Arthur. Chung @ sabah. gov. my; https: // orcid / org / 0000 - 0002 - 9529 - 4114 +hung@sabah.gov.my + + + +Author + +Wahab, Rodzay Bin Haji Abdul +Institute for Biodiversity and Environmental Research, Universiti Brunei Darussalam, Jalan Universiti, BE 1410, Brunei Darussalam. rodzay. wahab @ ubd. edu. bn; https: // orcid / org / 0000 - 0002 - 2151 - 7709 +rodzay.wahab@ubd.edu.bn + +text + + +Zootaxa + + +2021 + +2021-10-07 + + +5048 + + +3 + + +407 +421 + + + +journal article +4053 +10.11646/zootaxa.5048.3.6 +6456e942-b39b-4899-b2a9-f4deecde44d9 +1175-5326 +5556495 +AB9AF652-CA1B-4BB5-927F-BC3A12BA73D9 + + + + + + +Species group + +flori +Ingrisch, 1998 + + + + + + + +Remarks. +This species group currently consists of + +Ornebius fastus +Yang & Yen, 2001 + +from +Taiwan +, + +Ornebius flori +Ingrisch, 1998 + +and + +Ornebius marginatus +Ingrisch, 1998 + +from Sabah, + +Ornebius pullus +Ingrisch, 2006 + +from +Brunei +, and + +Ornebius xinyao +Tan, 2015 + +from +Singapore +. The species are characterised by the male phallic complex having the lateral valves membranous, dorso-ventrally compressed and acute apically; internal sclerites of medial valve almost forming a tube and with apex of ejaculatory duct truncated and little notched ( + +He +et al. +, 2021 + +). + + + + \ No newline at end of file diff --git a/data/38/52/D5/3852D52EFFCC3B28FF6EFDCAB594A470.xml b/data/38/52/D5/3852D52EFFCC3B28FF6EFDCAB594A470.xml new file mode 100644 index 00000000000..f71d388d8d1 --- /dev/null +++ b/data/38/52/D5/3852D52EFFCC3B28FF6EFDCAB594A470.xml @@ -0,0 +1,161 @@ + + + +New species and taxonomic notes of scaly crickets (Orthoptera: Mogoplistidae Mogoplistinae) from Borneo + + + +Author + +Tan, Ming Kai +Institut de Systématique, Evolution et Biodiversité (ISYEB), Muséum national d’Histoire naturelle, CNRS, SU, EPHE, UA, 57 rue Cuvier, CP 50, 75231 Paris Cedex 05, France. + + + +Author + +Japir, Razy +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Razy. Japir @ sabah. gov. my + + + +Author + +Chung, Arthur Y. C. +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Arthur. Chung @ sabah. gov. my; https: // orcid / org / 0000 - 0002 - 9529 - 4114 +hung@sabah.gov.my + + + +Author + +Wahab, Rodzay Bin Haji Abdul +Institute for Biodiversity and Environmental Research, Universiti Brunei Darussalam, Jalan Universiti, BE 1410, Brunei Darussalam. rodzay. wahab @ ubd. edu. bn; https: // orcid / org / 0000 - 0002 - 2151 - 7709 +rodzay.wahab@ubd.edu.bn + +text + + +Zootaxa + + +2021 + +2021-10-07 + + +5048 + + +3 + + +407 +421 + + + +journal article +4053 +10.11646/zootaxa.5048.3.6 +6456e942-b39b-4899-b2a9-f4deecde44d9 +1175-5326 +5556495 +AB9AF652-CA1B-4BB5-927F-BC3A12BA73D9 + + + + + + + +Ectatoderus angusticollis +Chopard, 1969 + + + + + + + + + + +Ectatoderus angusticollis +Chopard, 1969: 193 + + + + + + + +Ectatoderus angusticollis +— + + +Tan, 2012: 58 + +; Tan +et al. +, 2015: 48; + +Tan, 2017: 57 + + + + + + +Material examined (image). + + +Holotype + +, male, +SINGAPORE +, coll. +C. F. Baker +(MNHN-EO-ENSIF4487). + + + +Material examined. + +2 males +(F4.F.12, H12.F.05), +SINGAPORE +, +Mandai +, secondary forest +between Mandai Road and Upper Seletar Reservoir +, + +16–26 November 2015 + +, night, coll. +M. K. Tan +( +ZRC +) + +; + +2 males +( +ZRC +.ORT.467), +SINGAPORE +, +Lower Pierce Reservoir Park +, secondary forest, + +10 August 2012 + +, coll. +M. K. Tan. + + + + + \ No newline at end of file diff --git a/data/38/52/D5/3852D52EFFCC3B2DFF6EFAC7B1ABA181.xml b/data/38/52/D5/3852D52EFFCC3B2DFF6EFAC7B1ABA181.xml new file mode 100644 index 00000000000..f0decb9c648 --- /dev/null +++ b/data/38/52/D5/3852D52EFFCC3B2DFF6EFAC7B1ABA181.xml @@ -0,0 +1,348 @@ + + + +New species and taxonomic notes of scaly crickets (Orthoptera: Mogoplistidae Mogoplistinae) from Borneo + + + +Author + +Tan, Ming Kai +Institut de Systématique, Evolution et Biodiversité (ISYEB), Muséum national d’Histoire naturelle, CNRS, SU, EPHE, UA, 57 rue Cuvier, CP 50, 75231 Paris Cedex 05, France. + + + +Author + +Japir, Razy +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Razy. Japir @ sabah. gov. my + + + +Author + +Chung, Arthur Y. C. +Forest Research Centre (Sepilok), Sabah Forestry Department, P. O. Box 1407, 90715 Sandakan, Sabah. & Arthur. Chung @ sabah. gov. my; https: // orcid / org / 0000 - 0002 - 9529 - 4114 +hung@sabah.gov.my + + + +Author + +Wahab, Rodzay Bin Haji Abdul +Institute for Biodiversity and Environmental Research, Universiti Brunei Darussalam, Jalan Universiti, BE 1410, Brunei Darussalam. rodzay. wahab @ ubd. edu. bn; https: // orcid / org / 0000 - 0002 - 2151 - 7709 +rodzay.wahab@ubd.edu.bn + +text + + +Zootaxa + + +2021 + +2021-10-07 + + +5048 + + +3 + + +407 +421 + + + +journal article +4053 +10.11646/zootaxa.5048.3.6 +6456e942-b39b-4899-b2a9-f4deecde44d9 +1175-5326 +5556495 +AB9AF652-CA1B-4BB5-927F-BC3A12BA73D9 + + + + + + + +Ornebius pullus +Ingrisch, 2006 + + + + + + + +( +Figs. 8–10 +) + + + + + + + +Ornebius pullus +Ingrisch, 2006: 157 + + + + + + + +Ornebius pullus +— + + + +He +et al. +, 2021: 88 + + + + + + + +Ornebius +cf. +pullus + +— + +Tan, 2012: 34 + +; + +Tan & Ingrisch, 2013: 25 + +; + +Tan, 2017: 55 + +; Tan, 2019: 335 + + + + + +Material examined. + +1 male +( +BRU +.19.13), +BRUNEI DARUSSALAM +, +Belait District +, +Jalan Labi +near +Andulau Forest Reserve +, +N4.62238 +, +E114.51047 +, 101.3± + +6.4 m + +.a.s.l., on foliage, + +24 February 2019 + +, 2052h, coll. +M. K. Tan +& +H. Yeo +( +ZRC +) + +; + +1 male +( +BRU +.19.74), +BRUNEI DARUSSALAM +, +Belait District +, +Jalan Labi +near +Andulau Forest Reserve +, +N4.63352 +, +E114.51061 +, 89.0±7.1, on foliage, + +8 July 2019 + +, 2119h, coll. +M. K. Tan +( +UBDM +) + +. + + +Other material examined. + +1 male +(D18.F.03), +SINGAPORE +, +Mandai +, secondary forest +between Mandai Road and Upper Seletar Reservoir +, + +13 November 2015 + +, night, coll. +M. K. Tan +( +ZRC +) + +. + + + + +Remarks. +The male specimens from +Belait District +agree with the original description of + +O. pullus + +(see +Ingrisch, 2006 +) from +Brunei-Muara District +of +Brunei Darussalam +by habitus, size ( +Figs. 8 +, +9 +), shapes and colours of the epiproct and the paraproct process, as well as by the shape of phallic complex. However, the colour of the tegmen can be variable. While in +one male +(BRU.19.13) the colouration of the tegmen agrees with that of the +holotype +from +Brunei-Muara +, in the other male (BRU.19.74) the colour of the tegmen is somewhat intermediate between those of + +O. pullus + +and + +O. flori + +from Kinabalu in Sabah. + + + +FIGURE 7. + +Ectatoderus nigrofasciatus +Tan & Wahab + +, + +sp. nov. + +male phallic complex in dorsal (A), ventral (B), lateral (C) and latero-ventral (D) views; and apex of medial valve in ventral view (E). Scale bars: 1 mm (A—D), 0.5 mm (E). + + + + +FIGURE 8. + +Ornebius pullus +Ingrisch, 2006 + +males in their natural habitats in Belait: BRU.19.13 (A) BRU.19.74 (B). + + + + +FIGURE 9. + +Ornebius pullus +Ingrisch, 2006 + +male habitus in dorsal view: Belait (A, B) and Singapore (C). Scale bar: 1 mm. + + + +Tan & Ingrisch (2013) +previously noted that this species may have also occurred in +Singapore +, although there are some variations from the Bruneian specimens. Specifically, the apices of the membranous lateral valves of the male phallic complex can vary in their length and prominence and the tegmen colouration of the +Singapore +specimens is darker than those from +Brunei +( +Fig. 10 +). + + +We postulate that + +O. pullus + +from +Brunei +and +Singapore +may either represent a species complex or a polymorphic species. Molecular phylogeny may be useful to resolve this problem. + + + + +Distribution. +Within +Brunei Darussalam +, this species can be found in the western areas (i.e., +Belait +and +Brunei-Muara +Districts, it is probably also found in +Tutong District +between +Belait +and +Brunei-Muara +), but not in the eastern part of +Brunei +(i.e., +Temburong District +) (see +Tan & Wahab, 2018 +). One potential explanation is that + +O. pullus + +is found in the flatter terrains in +Belait +and Brunei-Maura Districts rather than the hilly terrains of +Temburong District +. + + + + \ No newline at end of file diff --git a/data/38/54/04/385404C5AC1F5D54B9682C64B2BF5092.xml b/data/38/54/04/385404C5AC1F5D54B9682C64B2BF5092.xml new file mode 100644 index 00000000000..cadeb954a0c --- /dev/null +++ b/data/38/54/04/385404C5AC1F5D54B9682C64B2BF5092.xml @@ -0,0 +1,104 @@ + + + +An annotated checklist of grasshoppers (Orthoptera, Acridoidea) from Mongolia + + + +Author + +Gankhuyag, Enkhtsetseg +Department of Biology, Teachers College, and Institute for Phylogenomics and Evolution, Kyungpook National University, Daegu 41566, South Korea + + + +Author + +Dorjsuren, Altanchimeg +Institute of Biology, Mongolian Academy of Sciences, Ulaanbaatar 133330, Mongolia & College of Life Sciences, Inner Mongolia University, Hohhot, 010031, China + + + +Author + +Choi, Eun Hwa +Department of Biology, Teachers College, and Institute for Phylogenomics and Evolution, Kyungpook National University, Daegu 41566, South Korea + + + +Author + +Hwang, Ui Wook +https://orcid.org/0000-0002-9735-8716 +Institute for Korean Herb-Bio Convergence Promotion, Kyungpook National University, Daegu 41566, South Korea & Institute of Phylogenomics and Evolution, and Department of Biology, Teachers College Kyungpook National University, Daegu 41566, Republic of Korea & School of Industrial Technology Advances, Kyungpook National University, Daegu 41566, South Korea & Phylomics Inc., Daegu 41910, South Korea +uwhwang@knu.ac.kr + +text + + +Biodiversity Data Journal + + +2023 + +2023-03-13 + + +11 + + +96705 +96705 + + + + +http://dx.doi.org/10.3897/BDJ.11.e96705 + +journal article +http://dx.doi.org/10.3897/BDJ.11.e96705 +1314-2828-11-e96705 +4617927B23675D59913B38550B7D9972 + + + + +Stenobothrus carbonarius (Eversmann, 1848) + + + +Native status + +Distribution in the natural zone +: Forest steppe. + + + +Distribution + +in Mongolia +: Sel. +Sergeev (1995) +:246, +Childebaev and Storozhenko (2001) +:31, +Batnaran (2008) +:47, +Batnaran et al. (2016) +:36, +Popova et al. (2020) +:600, +Batkhuyag and Batnaran (2021) +:69. + + +Global distribution +: Mongolia ( +Childebaev and Storozhenko 2001 +), Tuva, SE European Russia, S Siberia (up to Buryatia), Kazakhstan ( +Sergeev et al. 2019 +). + + + + \ No newline at end of file diff --git a/data/38/54/7D/38547DF84D4C59929EB22DB9DDB19E9D.xml b/data/38/54/7D/38547DF84D4C59929EB22DB9DDB19E9D.xml new file mode 100644 index 00000000000..8221bda36e9 --- /dev/null +++ b/data/38/54/7D/38547DF84D4C59929EB22DB9DDB19E9D.xml @@ -0,0 +1,310 @@ + + + +Chayamaritia vietnamensis (Gesneriaceae), a new species from Son La Province, northern Vietnam + + + +Author + +Xin, Zi-Bing +https://orcid.org/0000-0002-0062-6930 +Guangxi Key Laboratory of Plant Conservation and Restoration Ecology in Karst Terrain, Guangxi Institute of Botany, Guangxi Zhuang Autonomous Region and Chinese Academy of Sciences, CN- 541006, Guilin, China & Gesneriad Conservation Center of China (GCCC), National Gesneriaceae Germplasm Bank of GXIB, Guilin Botanical Garden, Guangxi Zhuang Autonomous Region and Chinese Academy of Sciences, CN- 541006 Guilin, China & Gesneriad Committee, China Wild Plant Conservation Association, CN- 541006, Guilin, China + + + +Author + +Fu, Long-Fei +https://orcid.org/0000-0001-8708-4718 +Guangxi Key Laboratory of Plant Conservation and Restoration Ecology in Karst Terrain, Guangxi Institute of Botany, Guangxi Zhuang Autonomous Region and Chinese Academy of Sciences, CN- 541006, Guilin, China & Gesneriad Conservation Center of China (GCCC), National Gesneriaceae Germplasm Bank of GXIB, Guilin Botanical Garden, Guangxi Zhuang Autonomous Region and Chinese Academy of Sciences, CN- 541006 Guilin, China & Gesneriad Committee, China Wild Plant Conservation Association, CN- 541006, Guilin, China + + + +Author + +Maciejewski, Stephen +Gesneriad Conservation Center of China (GCCC), National Gesneriaceae Germplasm Bank of GXIB, Guilin Botanical Garden, Guangxi Zhuang Autonomous Region and Chinese Academy of Sciences, CN- 541006 Guilin, China & The Gesneriad Society, 2030 Fitzwater Street, Philadelphia, PA, 19146 - 1333, USA + + + +Author + +Huang, Zhang-Jie +https://orcid.org/0000-0002-2288-6952 +Guangxi Key Laboratory of Plant Conservation and Restoration Ecology in Karst Terrain, Guangxi Institute of Botany, Guangxi Zhuang Autonomous Region and Chinese Academy of Sciences, CN- 541006, Guilin, China & Gesneriad Conservation Center of China (GCCC), National Gesneriaceae Germplasm Bank of GXIB, Guilin Botanical Garden, Guangxi Zhuang Autonomous Region and Chinese Academy of Sciences, CN- 541006 Guilin, China + + + +Author + +Do, Truong Van +https://orcid.org/0000-0002-0585-5513 +Vietnam National Museum of Nature, Vietnam Academy of Science & Technology, 18 Hoang Quoc Viet, Hanoi, Vietnam & Graduate University of Science and Technology, Vietnam Academy of Science & Technology, 18 Hoang Quoc Viet, Hanoi, Vietnam +dovantruong_bttn@yahoo.com + + + +Author + +Wen, Fang +https://orcid.org/0000-0002-3889-8835 +Guangxi Key Laboratory of Plant Conservation and Restoration Ecology in Karst Terrain, Guangxi Institute of Botany, Guangxi Zhuang Autonomous Region and Chinese Academy of Sciences, CN- 541006, Guilin, China & Gesneriad Conservation Center of China (GCCC), National Gesneriaceae Germplasm Bank of GXIB, Guilin Botanical Garden, Guangxi Zhuang Autonomous Region and Chinese Academy of Sciences, CN- 541006 Guilin, China & Gesneriad Committee, China Wild Plant Conservation Association, CN- 541006, Guilin, China +wenfang760608@139.com + +text + + +PhytoKeys + + +2021 + +2021-05-12 + + +177 + + +43 +53 + + + + +http://dx.doi.org/10.3897/phytokeys.177.63401 + +journal article +http://dx.doi.org/10.3897/phytokeys.177.63401 +1314-2003-177-43 +8CE2464D2EDF5F4092BFB1306F02BC01 + + + + +Chayamaritia vietnamensis F.Wen, T.V.Do, Z.B.Xin & S.Maciej +sp. nov. +Figs 2 +, 3C + + + +Diagnosis. + +The new species can be easily distinguished from the known + +Chayamaritia + +species by its peltate leaf blades. Besides, it differs from + +C. banksiae + +by its leaf blades apex rounded and margin entire (vs. apex shortly acuminate and margin minutely dentate); bracts 3, apex rounded and margin entire (vs. 2, apex acuminate and margin dentate); calyx lobes inside glabrous and margin entire (vs. inside with white appressed hairs in upper half, margin coarsely dentate); corolla lobes margin entire (vs. margin being minutely dentate); lateral staminodes 2.5-4 mm long (vs. 5.5-11 mm long). It also differs from + +C. smitinandii + +by its leaf blades apex rounded and margin entire (vs. apex acuminate and margin minutely dentate); bracts 3, ovate narrow and apex rounded (vs. 2, narrowly elliptic to lanceolate, somewhat falcate, apex acuminate); calyx lobes inside glabrous and margin entire (vs. inside densely pubescent, margin slightly toothed or appearing as large sessile glands on margin). + + + + +Type +. + + + +Vietnam +. +Son La Province +: +Moc Chau District +, +Xuan Nha Nature Reserve +, +20°43'N +, +104°40'E +, elev. ca. + +850 m + +, +31 October 2019 +, + +F. Wen + +, + +T.V. Do + +, + +Z.B. Xin + +& + +S. Maciejewski + +, +VMN-CN1214 +( +Holotype +: VNMN!; Isotypes: IBK!, VNMN!) + +. + + + +Description. + +Herbs perennial, rhizomatous prostrate thickened stem. +Leaves +basal, alternately arranged, numerous; +petioles +cylindrical, 10-25 cm long, 6-8 mm in diameter, densely covered with short white appressed hairs; +leaf blade +ovate to elliptic, peltate, 12-20 +x +10-15 cm, 1.2-1.3 times as long as wide, both surfaces densely covered with short white appressed hairs, base rounded, apex rounded, margin entire; lateral veins 6-9 on each side of the mid-rib, impressed on the adaxial surface, prominent on the abaxial surface. +Inflorescences +cymose, all axes and bracts pale green with red appressed hairs; cymes 4-6, axillary, 1-3-branched, 2-12-flowered; +peduncle +15-25 cm long, 4-6 mm in diameter, scattered villous; +bracts +3, narrow ovate, 1.3-1.6 cm long, 5-6 mm wide, adaxially sparsely villous, abaxially densely villous, margin entire, apex rounded; +pedicel +2.5-3.5 cm long, 1.5-2 mm in diameter, spreading puberulent. +Calyx +5-parted nearly to the base, strongly imbricate; +lobes +ovate, ca. 1.3 cm long, ca. 6 mm wide, appressed villous outside, glabrous inside, margin entire, apex acuminate. +Corolla +5.5-6.5 cm long, dark purple throughout outside, white to pale purple with two parallel yellow lines ventrally inside, lobes purple outside and inside, paler at base; +tube +3.5-4 cm long, 1-1.2 cm in diameter at the mouth, 6-8 mm in diameter at the base; +limb +distinctly 2-lipped, +adaxial lip +2-parted to over middle, lobes ca. 1 +x +1 cm, orbicular; +abaxial lip +3-parted to near the middle, lobes 1.3-1.5 +x +ca. 1 cm, oblong. +Stamens +2, adnate to ca. 2.2 cm above the base of the corolla tube; +filaments +1-1.2 cm long, white, sparsely pubescent, strongly geniculate at ca. 5 mm above the filament base, +anthers +ca. 2 mm long, sparsely pubescent. +Staminodes +3, lateral ones 2.5-4 mm long, white, glabrous, adnate to 1.8 cm above the base of the corolla tube, the middle one ca. 0.5-1 mm long, adnate to 1.2 cm above the base of the corolla tube. +Disc +orbicular, ca. 3 mm in height, 5-crenate at the margin, glabrous. +Pistil +4-4.5 cm long, +ovary +2.5-2.8 cm long, 2-2.5 mm in diameter, mixed pubescent and glandular-pubescent; +style +1-1.2 mm long, ca. 0.6 mm in diameter, mixed pubescent and glandular-pubescent; +stigma +only of lower lobe, bifid with blunt lobes, lobe ca. 3 mm long, ca. 0.5 mm in diameter. +Capsules +straight, 5.5-6.5 cm long, ca. 3.5-4 mm in diameter. + + + +Figure 2. + +Chayamaritia vietnamensis + +F.Wen, T.V.Do, Z.B.Xin & S.Maciej +A, B +habitat +C +habit +D +adaxial (top) and abaxial (bottom) surface of leaf blade +E +cymes +F +peduncle +G +adaxial (top) and abaxial (bottom) surface of bracts +H +pistil, calyx and lateral view of corolla +I +opened corolla with stamens and staminodes +J +stamens with cohering anthers +K +pistil +L +adaxial (top) and abaxial (bottom) surface of calyx lobes. Photos by Fang Wen, arranged by Zi-Bing Xin. + + + + +Phenology. +Flowering occurs from October to December and fruiting from November to January. + + +Etymology. + +The specific epithet " + +Chayamaritia vietnamensis + +" is derived from Vietnam, which holds the first discovered and only known location for the species. + + + +Figure 3. +Three species of + +Chayamaritia + +A + +C. banksiae + +D.J.Middleton +B + +C. smitinandii + +(B.L.Burtt) D.J.Middleton +C + +C. vietnamensis + +F.Wen, T.V.Do, Z.B.Xin & S.Maciej. Photos by Fang Wen, arranged by Zi-Bing Xin. + + + + +Distribution and habitat. + + +Chayamaritia vietnamensis + +is hitherto only known from the type locality, Xuan Nha Nature Reserve, Moc Chau District, Son La Province, northern Vietnam. It grows on rock surfaces surrounded by limestone areas in a subtropical evergreen seasonal rain forest. + + + +Conservation status. + + +Chayamaritia vietnamensis + +is known from two small-sized populations in the Xuan Nha Nature +Reserve's +buffer zone. The EOO and AOO of the new species are about 6.15 km2 and 2.2 km2, respectively. Furthermore, the natural habitat is mostly disturbed by local farmers who impose intense pressure on the remaining primary forest patches, by converting the natural habitat of the species into cornfields. Thus, following the IUCN Red List Categories and Criteria ( +IUCN 2019 +), it is provisionally assessed as endangered (EN B1ab(iii), B2ab(iii)) + + + + \ No newline at end of file diff --git a/data/38/54/84/385484D4F8D5037DAC2607F330520B81.xml b/data/38/54/84/385484D4F8D5037DAC2607F330520B81.xml new file mode 100644 index 00000000000..a98fb297225 --- /dev/null +++ b/data/38/54/84/385484D4F8D5037DAC2607F330520B81.xml @@ -0,0 +1,105 @@ + + + +The " Martian " flora: new collections of vascular plants, lichens, fungi, algae, and cyanobacteria from the Mars Desert Research Station, Utah + + + +Author + +Sokoloff, Paul C. + + + +Author + +Freebury, Colin E. + + + +Author + +Hamilton, Paul B. + + + +Author + +Saarela, Jeffery M. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8176 +8176 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8176 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8176 +1314-2828--8176 + + + + +Placidium lachneum (Ach.) Breuss + + + +Materials + + +Type status: +Other material +. Occurrence: recordNumber: 305c; recordedBy: +Sokoloff, Paul C. +; Taxon: scientificName: Placidiumlachneum (Ach.) Breuss; kingdom: Fungi; phylum: Ascomycota; class: Eurotiomycetes; order: Verrucariales; family: Verrucariaceae; genus: Placidium; specificEpithet: lachneum; taxonRank: Species; scientificNameAuthorship: (Ach.) Breuss; Location: continent: North America; country: +United States of America +; countryCode: USA; stateProvince: Utah; county: Wayne County; municipality: Hanksville; locality: +Mars Desert Research Station +; verbatimLocality: Alluvial plain and dry creekbed directly opposite turnoff to Mars Desert Research Station on Cow Dung Road; verbatimElevation: +1357 m +; verbatimLatitude: +38°24'19.2"N +; verbatimLongitude: +110°47'20"W +; geodeticDatum: WGS84; coordinateUncertaintyInMeters: 50; Identification: identifiedBy: +Freebury, Colin E. +; dateIdentified: 2015; Event: verbatimEventDate: +November 24, 2014 +; habitat: Sandstone rubble on sandy plain; Record Level: institutionID: CMN; collectionID: CANL 127972; collectionCode: +CANL +; basisOfRecord: Preserved Specimen + + + + +Notes + +This soil crust lichen is common in the Great Basin desert shrub lands and on the Colorado Plateau ( +St. Clair et al. 1991 +). The lower cortex is comprised of a distinct layer of globular cells, 20-70 +μm +high, with the lowermost cells brown to black. +Breuss (2002) +describes the lower cortex with angular cells in distinct vertical columns. +McCune and Rosentreter (2007) +provide a photo that shows +/- globular cells in a non-aligned pattern. Brodo et al. (2016) describe the cells of the lower cortex as spherical and sometimes in vertical columns, which corresponds well with our specimen (Fig. 20b). Other key characteristics of +Placidium lachneum +include the presence of marginal pycnidia and hyphal wefts that help to attach the lichen to the soil, as shown in Fig. 22c. + +Supplemental File: CANL 127972 (Suppl. material 21). + + + \ No newline at end of file diff --git a/data/38/55/07/385507CD90538F2D2C9E5329D28E7538.xml b/data/38/55/07/385507CD90538F2D2C9E5329D28E7538.xml new file mode 100644 index 00000000000..643a0397bba --- /dev/null +++ b/data/38/55/07/385507CD90538F2D2C9E5329D28E7538.xml @@ -0,0 +1,508 @@ + + + +Order Rodentia - Family Muridae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 2 + + + +1189 +1531 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316535 + + + + + +Niviventer fulvescens +(Gray 1847) + + + + + + + +[Niviventer] fulvescens +(Gray 1847) + +, + +Cat. Hodgson Coll. Brit. +Mus +.: 18 + + +. + + + + +Type Locality: + +Nepal +. + + + + + +Vernacular Names: +Indomalayan Niviventer +. + + + + +Synonyms: + +Niviventer baturus +(Sody 1932) + +; + +Niviventer besuki +( +Sody 1931 +) + +; + +Niviventer blythi +( +Kloss 1917 +) + +; + +Niviventer bukit +(Bonhote 1903) + +; + +Niviventer caudatior +(Hodgson 1849) + +; + +Niviventer cinnamomeus +( +Blyth 1859 +) + +; + +Niviventer condorensis +(Kloss 1926) + +; + +Niviventer flavipilis +( +Shih 1930 +) + +; + +Niviventer gracilis +(Miller 1913) + +; + +Niviventer huang +(Bonhote 1905) + +; + +Niviventer jacobsoni +( +Bartels 1937 +) + +; + +Niviventer jerdoni +(Blyth 1863) + +; + +Niviventer lepidus +(Miller 1913) + +; + +Niviventer lepturoides +(Sody 1934) + +; + +Niviventer lieftincki +( +Chasen 1939 +) + +; + +Niviventer ling +(Bonhote 1905) + +; + +Niviventer marinus +(Kloss 1916) + +; + +Niviventer mekongis +( +Robinson and Kloss 1922 +) + +; + +Niviventer minor +( +Shih 1930 +) + +; + +Niviventer octomammis +(Gray 1863) + +; + +Niviventer orbus +(Robinson and Kloss 1914) + +; + +Niviventer temmincki +( +Kloss 1921 +) + +; + +Niviventer treubii +(Robinson and Kiloss 1919) + +; + +Niviventer vulpicolor +(G. M. +Allen 1926 +) + +; + +Niviventer wongi +(Shih 1931) + +. + + + + +Distribution: +From S Himalayas ( +Nepal +and N +India +; see +Agrawal, 2000 +, for Indian distribution; +Corbet and Hill, 1992 +extend range to N +Pakistan +, but we have not seen any specimens from that region) through +Bangladesh +, S +China +( +Wang, 2003 +; including +Hainan +Isl and +Hong Kong +), and Indochina (including Con Son Isl and several other islands off coast of +Vietnam +; +Kuznetsov, 2000 +; Musser and Lunde, ms) to the Sunda Shelf on Peninsular +Thailand +(and offshore Koh Chang), Malay Peninsula (and offshore Koh Samui), Sumatra, Java, and Bali; absent from Borneo and other islands on the Sunda Shelf. Because samples of + +N. fulvescens + +have been confused with those of + +N. confucianus + +, + +N. niviventer + +, and + +N. tenaster + +in museum collections and the literature, the range outlined here derives primarily from Musser’s identification of specimens in +AMNH +, +ANSP +, +BMNH +, +FMNH +, +HUNHM +, +MCZ +, +MNHN +, +MZB +, +RMBR +, +RMNH +, +USNM +, and +ZFMK +. + + + + +Conservation: +IUCN +– Lower Risk (lc). + + + + +Discussion: + +Some authors have referred to populations on Bali, Java, Sumatra, Malay Peninsula, and peninsular +Thailand +as either + +N. rapit +( +Chasen, 1940 +) + +or + +N. bukit + +( +Corbet and Hill, 1992 +; J. +T +. Marshall, Jr., 1977 +a +; + +Musser, 1981 +b + +), and those occurring north of the Isthmus of Kra as + +N. fulvescens + +, pending taxonomic revision of the group. Abe’s (1983) study, which focused on Thai samples, and recent morphometric analyses combining Indochinese and Sundaic samples (Musser and Lunde, ms) support the hypothesis that specimens of + +bukit + +represent + +N. fulvescens +( +Abe, 1983 +) + +, an arrangement reflecting the earlier view of +Ellerman (1941) +and particularly +Osgood (1932:305) +: "The relationship of + +fulvescens + +to southern forms is obvious in several instances, especially in that of + +R +. f. +bukit + +which can at most be no more than a subspecies." This hypothesis will require additional testing with other data sets, including DNA sequences. The morphometric study by Musser and Lunde (ms) also demonstrates that + +N. fulvescens + +is part of a tight cluster containing the Thai endemic + +N. hinpoon + +, and the Sumatran + +N. fraternus + +, another phylogenetic pattern that will have to be tested by analyses of other kinds of morphological traits and gene sequences. Analysis of mtDNA cytochrome +b +sequences indicateed + +N. fulvescens + +to be phyletically closer to a monophyletic clade containing + +N. tenaster + +, + +N. coninga + +, + +N. confucianus + +, and + +N. culturatus + +than is + +N. langbianis + +(J. L. Patton, in litt., 2000; no other + +Niviventer + +were sampled). Neithammer and Martens (1975) regarded + +fulvescens + +to be only a color morph of + +N. niviventer + +in +Nepal +, but the two species are readily distinguished by pelage coloration and external, cranial, and dental dimensions ( +Abe, 1977 +; Musser and Lunde, ms). + + +If Indochinese and Sundaic populations all represent + +N. fulvescens + +, then that species is the only member of the genus with a geographic distribution encompassing the Indochinese mainland and some islands on the Sunda Shelf; other murines with roughly equivalent ranges are + +Berylmys bowersii + +, + +Chiropodomys gliroides + +, + +Leopoldamys sabanus + +, and + +Maxomys surifer + +( +Musser and Newcomb, 1983 +; but see accounts of + +L. sabanus + +and + +M. surifer + +). Spermatozoal morphology of Malay Peninsula sample described by +Breed and Yong (1986 +, as + +bukit + +) in comparative context. Chromosomal data for samples from +Vietnam +, +Thailand +, Malaya, Java, and +Hong Kong +summarized by +Baskevich and Kuznetsov (2000) +. Biology, habitat, morphological variation, and taxonomy described by +Abe (1971 +, +1977 +) for samples from C +Nepal +. Ecological relationships with + +N. confucianus + +and other murines in S +Yunnan +reported by +Wu et al. (1996) +. Vietnamese records and other information provided by +Dang et al. (1994) +, +Kuznetsov (2000) +and + +Lunde et al. (2003 +b +) + +. Fossils identified as + +N. fulvescens + +were recovered from late Pleistocene cave sediments in the Sichuan-Guizhou region of S +China +( +Zheng, 1993 +) + +. + + + + \ No newline at end of file diff --git a/data/38/55/52/3855520C25BAD4B7FA66DAF34A358944.xml b/data/38/55/52/3855520C25BAD4B7FA66DAF34A358944.xml new file mode 100644 index 00000000000..4543deb66ae --- /dev/null +++ b/data/38/55/52/3855520C25BAD4B7FA66DAF34A358944.xml @@ -0,0 +1,88 @@ + + + +Catalogue of Geadephaga (Coleoptera, Adephaga) of America, north of Mexico + + + +Author + +Bousquet, Yves +Agriculture and Agri-Food Canada, Central Experimental Farm, Ottawa, Ontario, Canada +bousquety1@yahoo.com + +text + + +ZooKeys + + +2012 + +2012-11-28 + + +245 + + +1 +1722 + + + + +http://dx.doi.org/10.3897/zookeys.245.3416 + +journal article +http://dx.doi.org/10.3897/zookeys.245.3416 +1313-2970-245-1 +FFFF52503A0AFF882450FFB66D45FF8E +578462 + + + + +Amara pterostichina Hayward, 1908 + + + + +Curtonotus putzeysi +Bates, 1878a: 600 [secondary homonym of + +Amara putzeysii + +Fairmaire, 1867 and + +Amara putzeysii + +Horn, 1875]. Type locality: "near the capital, Mexico" (original citation). Lectotype (♂), designated by Hieke (1993: 150), in BMNH. Etymology. The specific name was given in honor of the Belgian Jules Antoine Adolphe Henri Putzeys [1809-1882] who, despite his judicial and administrative duties, published extensively on botany and entomology, particularly Odonata and +Carabidae +. + + +Amara pterostichina +Hayward, 1908: 20. Type locality: "Coolidge [McKinley County], N[ew] M[exico]" (lectotype label). Lectotype (♂), designated by Hieke (1993: 149), in MCZ [# 25664]. Synonymy established by Hieke (1993: 149). + + +Amara batesiana +Csiki, 1929: 466. Replacement name for + +Amara putzeysi + +Bates, 1878. + + + +Distribution. +This species ranges from southern Arizona (Cochise County, CNC) to western Texas (Dajoz 2007: 23; Brewster and Jeff Davis Counties, CNC, MCZ), south to the Federal District and central Veracruz in Mexico (Bates 1882a: 76). + + +Records. + +USA +: AZ, NM, TX - Mexico + + + + \ No newline at end of file diff --git a/data/38/55/56/3855568A5281518E9B536CFE6824787D.xml b/data/38/55/56/3855568A5281518E9B536CFE6824787D.xml new file mode 100644 index 00000000000..91bcd78787b --- /dev/null +++ b/data/38/55/56/3855568A5281518E9B536CFE6824787D.xml @@ -0,0 +1,74 @@ + + + +New combinations in Neotropical Thelypteridaceae + + + +Author + +Salino, Alexandre +Departamento de Botanica, Universidade Federal de Minas Gerais, Av. Antonio Carlos, 6627 - Belo Horizonte, Minas Gerais, Brazil. Caixa Postal 486, CEP 30123 - 970 +salinobh@gmail.com + + + +Author + +Almeida, Thais E. +Programa de Ciencias Naturais, Instituto de Ciencias da Educacao - Universidade Federal do Oeste do Para, Avenida Marechal Rondon, s / n, Campus Rondon - Santarem, Para, Brazil 68040 - 070 + + + +Author + +Smith, Alan R. +University Herbarium, University of California, 1001 Valley Life Sciences Bldg. # 2465, Berkeley, CA 94720 - 2465, USA + +text + + +PhytoKeys + + +2015 + +2015-12-02 + + +57 + + +11 +50 + + + + +http://dx.doi.org/10.3897/phytokeys.57.5641 + +journal article +http://dx.doi.org/10.3897/phytokeys.57.5641 +1314-2003-57-11 +98412B4A8904FFAAFFD64239FFE1FF8E +576315 + + + + +Amauropelta inaequans (C.Chr.) Salino & T.E.Almeida +comb. nov. + + + + +Dryopteris euchlora (Sodiro) C.Chr. var. inaequans C.Chr. +, Kongel. Danske Vidensk. Selsk. Skr., Naturvidensk. Math. Afd., ser. 7, 10: 150. 1913. + + +Thelypteris inaequans (C.Chr.) Lellinger +, Amer. Fern J. 67(2): 60. 1977. + + + + \ No newline at end of file diff --git a/data/38/55/87/385587AAF7241171FF4CC059FBFBA704.xml b/data/38/55/87/385587AAF7241171FF4CC059FBFBA704.xml new file mode 100644 index 00000000000..645894a615e --- /dev/null +++ b/data/38/55/87/385587AAF7241171FF4CC059FBFBA704.xml @@ -0,0 +1,129 @@ + + + +Redescription of Rhyacophila clemens Tsuda 1940 (Trichoptera, Rhyacophilidae), with descriptions of five new, allied species from Japan + + + +Author + +Kawase, Naoki + +text + + +Zootaxa + + +2024 + +2024-05-03 + + +5447 + + +1 + + +55 +76 + + + + +http://dx.doi.org/10.11646/zootaxa.5447.1.3 + +journal article +295741 +10.11646/zootaxa.5447.1.3 +583af73b-a902-4006-999f-4aad27eba888 +1175-5326 +11119209 +3A9842EC-F3D2-4839-9731-AA79A27B25CB + + + + + + + +Rhyacophila clemens + +Species Group +Ross 1956 + + + + + + +In this study, I have recognized six Japanese species and one Korean species belonging to the + +R. clemens + +Species Group. As mentioned above in the introduction, the males of this species group are similar to those of the + +R. viquaea + +Species Group in having two pairs of anal sclerites, but the males of the seven species of the + +R. clemens + +Species Group in this study were distinguishable from those of the + +R. viquaea + +Species Group by the shape of the apical band: The apical band is large and oval in lateral view and independent of the root of the anal sclerites in the + +R. clemens + +Species Group ( +Figs 1H +, +3B +, +4D +, +5B +, +6B +, +7B +), but the ends of the apical band are joined with the root of the ventral pair of the anal sclerites in the + +R. viquaea + +Species Group ( +Ross 1956 +). +Schmid (1970) +treated the ventral pair of the anal sclerites in the + +R. viquaea + +Species Group as the apical band of the tergal strap, whereas +Lee & Ruiter (2011) +agreed with Ross’s interpretation. Furthermore, the male of each species in the + +R. clemens + +Species Group bears the apical hinged process on segment X posteroventrally and the ventral plate of the aedeagus, but those of the + +R. viquaea + +Species Group lack such a process and plate ( +Ross 1956 +, +Schmid 1970 +, +Lee & Ruiter 2011 +). Consequently, the male diagnostic characters for the + +R. clemens + +Species Group are as follows: Segment IX is long dorsally; the preanal appendages are absent; segment X bears an apical hinged process posteroventrally; two pairs of anal sclerites have a common internal root; a pair of large apical bands surrounds the anus and the root of the anal sclerites; the aedeagus bears a large sclerotized ventral plate; and parameres are absent. + + + + \ No newline at end of file diff --git a/data/38/55/87/385587AAF7261174FF4CC63EFD0CA06C.xml b/data/38/55/87/385587AAF7261174FF4CC63EFD0CA06C.xml new file mode 100644 index 00000000000..3262ec24b7c --- /dev/null +++ b/data/38/55/87/385587AAF7261174FF4CC63EFD0CA06C.xml @@ -0,0 +1,399 @@ + + + +Redescription of Rhyacophila clemens Tsuda 1940 (Trichoptera, Rhyacophilidae), with descriptions of five new, allied species from Japan + + + +Author + +Kawase, Naoki + +text + + +Zootaxa + + +2024 + +2024-05-03 + + +5447 + + +1 + + +55 +76 + + + + +http://dx.doi.org/10.11646/zootaxa.5447.1.3 + +journal article +10.11646/zootaxa.5447.1.3 +1175-5326 +11119209 +3A9842EC-F3D2-4839-9731-AA79A27B25CB + + + + + + + +Rhyacophila furcicauda + +sp. nov. + + + + + + +( +Figs 7A–7J +, +9D +) + + + + +Rhyacophila +sp. 2 + +( + +clemens + +gr.): + +Kawase & Morita 2010 +, 36. + + + + +Diagnosis. +The male genitalia of + +R. furcicauda + +sp. nov. +are unique among known species in the + +R. clemens + +Species Group in that the apical segment of each inferior appendage is bifurcate ( +Fig. 7A +) (those of the other species are not bifurcate). The female genitalia of + +R. furcicauda + +sp. nov. +are similar to those of + +R. parvicauda + +sp. nov. +in having thick setae densely on the lateral surface of segment VIII but can be distinguished from the latter by the characters given in the diagnosis for + +R. parvicauda +. + + + + + +FIGURE 7. + +Rhyacophila furcicauda + +sp. nov. + +7A–7F, male genitalia: 7A, left lateral; 7B, segment X and phallic apparatus, left lateral; 7C, same, posterodorsal; 7D, dorsal (left inferior appendage omitted); 7E, apical segment of right inferior appendage, mesal; 7F, segment X and phallic apparatus, ventral. 7G–7J, female genitalia: 7G, segment VIII, left lateral; 7H, same, ventral; 7I, vaginal apparatus, left lateral; 7J, same, ventral. Abbreviation: vr = ventral ridge. Arrows see text. + + + +Adult +. Length of each forewing: male +6.1–7.2 mm +(mean = 6.7, SD = 0.39, n = 8), female +6.7 mm +(n = 1). General morphology and coloration similar to those of + +R. clemens + +, but wing venation similar to + +R. inazui + +( +Fig. 4B +), root of fork I on each forewing clearly longer than that of fork II. + + +Male genitalia +( +Figs 7A–7F +). Segment IX dorsal half longer than ventral half in lateral view ( +Fig. 7A +), widely trapezoidal in dorsal view ( +Fig. 7D +); apicodorsal lobe extruded posterad, trapezoidal in dorsal view ( +Fig. 7D +), angular in lateral view ( +Fig. 7A +). Preanal appendages absent. Segment X reverse L-shaped in lateral view, composed of vertical part and horizontal part: vertical part tall in lateral view ( +Fig. 7B +); horizontal part oval in dorsal view ( +Fig. 7D +), apically bent upwards in lateral view ( +Figs 7A, 7B +); apical hinged process with pair of long finger-like lobes, parallel, directed posterodorsad ( +Figs 7A–7D, 7F +), with pair of round anteroventral corners and small protrusion between them ( +Fig. 7F +). Anal sclerites composed of two pairs of lobes, each long and rectangular, but apex of each ventral pair obliquely truncate in lateral view; these two pairs of lobes with common internal root ( +Fig. 7B +). Apical band well developed, semi-oval in lateral view, broadly surrounding anus and root of anal sclerites ( +Figs 7B, 7F +). Tergal band connecting base of apical band to dorsum of phallobase ( +Fig. 7B +). Basal segment of each inferior appendage setose, short, thick, nearly rectangular, posterior half gradually thicker in lateral view ( +Fig. 7A +). Apical segment of each inferior appendage bifurcate in lateral view ( +Figs 7A, 7E +), covered with hair-like setae sparsely laterally, with dense short spine-like setae on posteromesal margin of ventral fork ( +Figs 7A, 7D, 7E +). In phallic apparatus, phallobase short; aedeagus forming narrow tube with sclerotized ventral plate ( +Figs 7B, 7C +); ventral plate horizontal and long and tongue-shaped, posterior margin with small triangular protrusion apicomesally in ventral view ( +Fig. 7F +). Parameres absent. + + +Female genitalia +( +Figs 7G–7J +). Segment VIII annular, dorsal margin almost straight in lateral view ( +Fig. 7G +); pair of ventral ridges widely separated anteriorly, running subparallel posteriorly ( +Fig. 7H +); with many darkly pigmented and thick setae laterally, with fine pale short setae between ventral ridges ( +Figs 7G, 7H +); pair of apodemal rods reaching to posterior end of segment VI. Segment IX membranous, with pair of apodemal rods dorsolaterally, extending into abdominal segment VI. Vaginal apparatus simple; posterior process sclerotized, dorsal margin slightly convex in lateral view ( +Fig. 7I +), apparatus oval in ventral view ( +Fig. 7J +); processus spermathecae membranous ( +Figs 7I, 7J +). + + +Immature stage. +Unknown. + + + + + + +Holotype +. + +Male +(in alcohol), +Yuzurio-cho +, Higashi-ômi-shi, +Shiga Pref. +, +Honshu +, +Japan +, +35°4’40” N +136°23’44”E +, alt. + +370 m + +, + +31.v–26.vi.2009 + +, +N. Kawase +( +LBM1410012653 +). + + + + + +Paratypes +. +Honshu +: +Mie + +: +2 males +, +Okumano +, +Iga-shi +, + +9.vi–22.vi.2012 + +, +H. Morita +( +LBM1410012654– 1410012655 +) + +. + + +Wakayama + +: +2 males +, +Kôya-ryujin Skyline +, +Ryujin-mura +, + +28–29.v.2004 + +, (SPMN-IS-59800–59801); +2 males +, +1 female +, same data, +T +. +Hattori +( +LBM1410012656–1410012658 +) + +. + + +Other specimens examined. Honshu: + + +Mie + +: +1 male +, +Okumano +, +Iga-shi +, + +26.v–9.vi.2012 + +, +H. Morita +(NKa) + +; + +1 male +, +Hobo-cho +, +Kumano-shi +, +33°57’N +136°12’E +, + +31.v.2006 + +, +N. Kawase +(NKa) + +. + + +Nara + +: +1 pupa +(male), +Kannohgawa +, +Totsukawa-mura +, + +11.vi.2005 + +, +S. Kobayashi +( +SPMN +) + +; + +1 male +, +Kitozumi +, +Tenkawa-mura +, + +22.vii.2021 + +, +H. Iketake +( +HI +) + +. + + + + +Etymology +. The species name + +“furcicauda + +” (= fork tail) is a noun in apposition referring to the bifurcate apical segment of each inferior appendage in male genitalia. + + + + +Distribution and biology. + +Rhyacophila furcicauda + +sp. nov. +was collected from only Suzuka Mountains and Kii Mountains in Kinki district, central +Japan +( +Fig. 9D +). Adults of this species were collected near streamside by sweeping or using a Malaise trap in late May to July. + + +Japanese name. +Nimata-nagare-tobikera. + + + + \ No newline at end of file diff --git a/data/38/55/87/385587AAF7271177FF4CC19BFCECA06F.xml b/data/38/55/87/385587AAF7271177FF4CC19BFCECA06F.xml new file mode 100644 index 00000000000..5d3b4aad4aa --- /dev/null +++ b/data/38/55/87/385587AAF7271177FF4CC19BFCECA06F.xml @@ -0,0 +1,170 @@ + + + +Redescription of Rhyacophila clemens Tsuda 1940 (Trichoptera, Rhyacophilidae), with descriptions of five new, allied species from Japan + + + +Author + +Kawase, Naoki + +text + + +Zootaxa + + +2024 + +2024-05-03 + + +5447 + + +1 + + +55 +76 + + + + +http://dx.doi.org/10.11646/zootaxa.5447.1.3 + +journal article +10.11646/zootaxa.5447.1.3 +1175-5326 +11119209 +3A9842EC-F3D2-4839-9731-AA79A27B25CB + + + + + + + +Rhyacophila kumgangsanica +Kumanski 1990 + + + + + + + +( +Figs 8A–8D +) + + + + + +Rhyacophila kumgangsanica +Kumanski 1990 + +, 41–42, male ( +Type +locality: Mt. Kumgang-san in +North Korea +); +Park & Kong 2020 +, 300, list. + + +Specimens examined. + +2 males +, +Myeonji Mt. valley +, +Gapyeong-gun +, +Gyeonggi-do +, +Korea +, +37°56’11”N +127°28’51”E +, alt. + +250 m + +, + +3.vi.2014 + +, +T +. Nozaki (NKa) + +. + + + + + +FIGURE 8. + +Rhyacophila kumgangsanica +Kumanski 1990 + + +. 8A–8D, male genitalia: 8A, left lateral; 8C, dorsal (left inferior appendage omitted); 8B, segment X and phallic apparatus, left lateral; 8D, same, ventral. + + + + +Distribution. + +Rhyacophila kumgangsanica + +is distributed on the Korean Peninsula ( +Park & Kong 2020 +). + + + + +Remarks +. The male genitalia of this species were precisely described by +Kumanski (1990) +based on specimens collected from +North Korea +. +Hattori (2005) +suggested that this species probably belongs to the + +R. clemens + +Species Group. The male genitalia of this species are very similar to those of the Japanese species described or redescribed above in having the following characters: The horizontal part of segment X bears the apical hinged process ventrally ( +Figs 8A, 8B, 8D +); two pairs of anal sclerites have a common internal root ( +Fig. 8B +); a pair of large apical bands surrounds the anus and the root of the anal sclerites ( +Figs 8B, 8D +); and the narrow aedeagus bears a large, long ventral plate ( +Fig. 8B +). Thus + +R. kumgangsanica + +definitely belongs to the + +R. clemens + +Species Group. + + +This species is easily distinguished from Japanese species of this species group by the shapes of the apical segment of each inferior appendage and the apical hinged process of segment X: (1) the apical segment of each inferior appendage is rectangular in lateral view ( +Fig. 8A +); (2) the apical hinged process of segment X bears a pair of long lanceolate lobes in dorsal and ventral views ( +Figs 8B, 8C +). + + + + \ No newline at end of file diff --git a/data/38/55/87/385587AAF730116CFF4CC19BFBCEA3D8.xml b/data/38/55/87/385587AAF730116CFF4CC19BFBCEA3D8.xml new file mode 100644 index 00000000000..e00bd614c6c --- /dev/null +++ b/data/38/55/87/385587AAF730116CFF4CC19BFBCEA3D8.xml @@ -0,0 +1,1447 @@ + + + +Redescription of Rhyacophila clemens Tsuda 1940 (Trichoptera, Rhyacophilidae), with descriptions of five new, allied species from Japan + + + +Author + +Kawase, Naoki + +text + + +Zootaxa + + +2024 + +2024-05-03 + + +5447 + + +1 + + +55 +76 + + + + +http://dx.doi.org/10.11646/zootaxa.5447.1.3 + +journal article +10.11646/zootaxa.5447.1.3 +1175-5326 +11119209 +3A9842EC-F3D2-4839-9731-AA79A27B25CB + + + + + + + +Rhyacophila vesperalis + +sp. nov. + + + + + + +( +Figs 3A–3K +, +9B +) + + + + + +Rhyacophila clemens + +: +Kobayashi 1959 +, 343, list; +Gyotoku & Nozaki 1992 +, 14, list. Misidentifications. + + + + +Rhyacophila clemens + +(variation) + +: +Hattori 2005 +, 423 (4d’ & 4e’ in Fig. 10), male & female; +Hattori 2018 +, 483 (4d’ & 4e’ in Fig. 11), male & female. + + + + + +Rhyacophila +sp. + +F + + +: +Nojima 2017 +, 111, list. + + + + + + + +Rhyacophila +sp. + + +14 + +: + +Yamamoto +et al +. 2021 + +, 70, list. + + + + + +FIGURE 3. + +Rhyacophila vesperalis + +sp. nov. + +3A–3E, male genitalia: 3A, left lateral; 3B, segment X and phallic apparatus, left lateral; 3C, dorsal (left inferior appendage omitted); 3D, ventral (left inferior appendage and apical segment of right inferior appendage omitted); 3E1, apical hinged process of segment X, enlarged, ventral; 3E2, ventral plate of aedeagus, enlarged, ventral. 3F–3K, female genitalia: 3F, left lateral; 3G, segment VIII, left lateral; 3H, same dorsal; 3I, same ventral; 3J, vaginal apparatus, left lateral; 3K, same, ventral. Arrows see text. + + + + +Diagnosis +. The male and female of this species are readily distinguishable from those of other Japanese species of this species group by the following genital characters: In the male, the apical hinged process of segment X bears a pair of long anteroventral longitudinal ridges (arrows in +Figs 3D, 3E +1 +); and in the female, segment VIII bears a pair of lateral flanges posterolaterally like short wings (arrows in +Figs 3G, 3H +). Additionally, the male of this species is somewhat similar to + +R. kumgangsanica +Kumanski 1990 + +, a Korean species ( +Fig. 8 +), but can be easily distinguished from the latter by the following character: The shape of each apical segment of the inferior appendage is subtriangular in + +R. vesperalis + +( +Fig. 3A +) but subrectangular in + +R. kumgangsanica + +( +Fig. 8A +) in lateral view. + + +Adult +. Length of each forewing: male +5.6–7.2 mm +(mean = 6.5, SD = 0.48, n = 29), female +6.8–8.6 mm +(mean = 7.8, SD = 0.53, n = 14). General morphology and coloration similar to those of + +R. clemens + +, wing venation of this species also similar to that of + +R. clemens + +( +Fig. 1D +). + + +Male genitalia +( +Figs 3A–3E +). Segment IX almost rectangular in dorsal view with tiny apicodorsal lobe ( +Fig. 3C +), dorsal half longer than ventral half in lateral view ( +Fig. 3A +). Preanal appendages absent. Segment X reverse L-shaped in lateral view composed of vertical part and horizontal part: vertical part tall in lateral view ( +Fig. 3B +); horizontal part sub-oval in lateral view ( +Fig. 3A +), sub-rectangular in dorsal view with posterior margin bilobed ( +Fig. 3C +); apical hinged process arising from horizontal part apicoventrally, with pair of long finger-like lobes posteriorly, with pair of anteroventral longitudinal ridges (arrows indicated in +Figs 3D, 3E +1 +). Anal sclerites composed of two pairs of lobes, with common internal root ( +Fig. 3B +), each long rectangular in lateral view, but apex of each ventral pair rather pointed ventrally ( +Fig. 3B +). Apical band well developed, semi-oval in lateral view, broadly surrounding anus and base of anal sclerites ( +Figs 3B, 3D +). Tergal band connected anteroventral part of apical band to dorsum of phallobase. Basal segment of each inferior appendage setose, elongate, posterior half gradually thicker in lateral view ( +Fig. 3A +). Apical segment of each inferior appendage subtriangular in lateral view ( +Fig. 3A +), densely covered with fine hair-like setae mesally ( +Fig. 3C +). In phallic apparatus, phallobase short, cup-like ( +Fig. 3B +); aedeagus forming narrow tube with sclerotized ventral plate ( +Figs 3B, 3D +); ventral plate tongue like with posterior margin roundly concave and tiny protrusion mesally in ventral view ( +Figs 3D, 3E +2 +). Parameres absent. + + +Female genitalia +( +Figs 3F–3K +). Segment VIII annular, bearing slightly angular dorsal bulge in lateral view; pair of posterolateral flanges like short wing (arrows in +Figs 3G, 3H +); with pair of ventral ridges closest in anterior 1/4–1/ +3 in +ventral view ( +Fig. 3I +); pair of apodemal rods reaching to middle of segment VI ( +Fig. 3F +). Segment IX membranous, with pair of apodemal rods dorsolaterally extending to abdominal segment VI or more deeply ( +Fig. 3F +). Vaginal apparatus simple; posterior process sclerotized, approximately three times as long as wide, dorsal margin round in lateral view ( +Fig. 3J +), long oval with pair of thin longitudinal wrinkles in ventral view; processus spermathecae membranous ( +Fig. 3K +). + + +Immature stage +. Unknown. + + + + + + +Holotype +. + +Male (in alcohol), Odamiyama-hontani, Nakagawa, Uchiko-cho, +33°32’14”N +132°52’29”E +, alt. + +990 m + +, + +10–20.iv.2021 + +, +E. Yamamoto +, +Ehime +, Shikoku, +JAPAN +( +LBM1410012590 +). + + + + + +Paratypes +. +Shikoku +: +Ehime + + +: + +1 male +, +1 female +, same locality as the holotype, + +19.v.2000 + +, +E. Yamamoto +( +LBM1410012591–1410012592 +) + +; + +1 male +, same locality as the holotype, + +10.v.2001 + +, +E.Yamamoto +(SPMN-IS-59744) + +; + +4 males +, +2 females +, same locality as the holotype, + +21.v.2001 + +, +E. Yamamoto +(SPMN-IS-59745–59750) + +; + +3 males +, +1 female +, same locality as the holotype, + +31.v.2001 + +, +E. Yamamoto +(SPMN-IS-59737–59740) + +; + +2 males +, +1 female +, same locality as the holotype, + +10.vi.2001 + +, +E. Yamamoto +(SPMN-IS-59741–59743) + +; + +2 males +, +3 females +, +Namakusadani +, +Odamiyama +, +Nakagawa +, +Uchiko-cho +, + +11–20.vi.2020 + +, +E. Yamamoto +( +LBM1410012596–1410012600 +) + +; + +1 male +, +2 females +, same locality as the holotype, + +11–20.vi.2021 + +, +E. Yamamoto +( +LBM1410012593–1410012595 +) + +; + +7 males +, +5 females +, +Odamiyama-hônomata +, +Nakagawa +, +Uchiko-cho +, +33°32’40”N +132°51’11”E +, alt. + +925 m + +, + +21–30.vi.2018 + +, +E. Yamamoto +( +OMNH +) + +; + + +Tokushima + +: +1 female +, +Kônose-kyo +, +Kitokitagawa +, +Naka-cho +, + +6.v.2009 + +, +T +. +Torii +(SPMN-IS-59751) + +. + + +Other specimens examined. Honshu: + + +Tottori + +: +1 male +, +Wakamatsu-gawa +, +Yukawa +, +Nichinan-cho +, + +15.ix.2002 + +, +T +. +Hattori +( +SPMN +) + +. + + +Shimane + +: +1 male +, +Takezaki-oidani +, +Okuizumo-cho +, + +19.v.1992 + +, +N. Nishimura +(NKa) + +. + + +Okayama + +: +10 males +, +Shingô-yuno +, +Niimi-shi +, + +1.vi.2013 + +, +K. Nojima +(NKa) + +. + + +Hiroshima + +: +1 male +, +Hosomi-dani +, +Yoshiwa +, +Hatsukaichi-shi +, + +7.vi.2004 + +, +I. Mori +( +SPMN +) + +; + +2 males +, same locality, + +7.vi–19.vii.2004 + +, +I. Mori +( +SPMN +) + +. + + +Yamaguchi + +: +1 male +, +Jiyoshi +, +Toyota-cho +, +Shimonoseki-shi +, + +22.v.1996 + +, +T +. +Hattori +( +SPMN +) + +. + + +Shikoku + +: + + + +Kagawa + +: +2 males +, +1 female +, +Koujigawa +, +Shionoe-cho +, +Takamatsu-shi +, + +23.v.2000 + +, +E. Yamamoto +( +SPMN +) + +. + + +Ehime + +: +1 female +, +Teppô-ishikawa Camp-village +, +Omogo-mura +, + +22–23.v.1999 + +, +A. Ohkawa +& +T +. +Ito +(in glycerin) ( +SPMN +) + +; + +1 female +, same data ( +SPMN +) + +; + +1 male +, +Jiyoshi-tôge +, +Yanadani +, +Kumakôgen-cho +, + +23.ix.2002 + +, +T +. +Hattori +(in glycerin) ( +SPMN +) + +; + +2 males +, +5 females +, Odamiyama-Tarô-dani, +Uchiko-cho +, + +20.v.2000 + +, +E. Yamamoto +( +SPMN +) + +; + +1 male +, +2 females +, +Odamiyama-Namakusadani +, +Uchiko-cho +, + +26.vii.1998 + +, +E. Yamamoto +( +SPMN +) + +; + +1 male +, same locality, + +29.v.1999 + +, +E. Yamamoto +(in glycerin) ( +SPMN +) + +; + +4 males +, +1 female +, same locality, + +21.vi.1999 + +, +E. Yamamoto +(NKa) + +; + +6 males +, +4 females +, same locality, + +5.vi.2000 + +, +E. Yamamoto +( +SPMN +) + +; + +5 males +, +4 females +, same locality, + +16.vi.2000 + +, +E. Yamamoto +( +SPMN +) + +; + +1 female +, same locality, + +29.vi.2000 + +, +E. Yamamoto +( +SPMN +) + +; + +2 males +, same locality, + +8.vii.2000 + +, +E. Yamamoto +( +SPMN +) + +; + +3 males +, +1 female +, same locality, + +16.vii.2000 + +, +E. Yamamoto +( +SPMN +) + +; + +2 males +, +1 female +, +Oda-koyayama +, +Oda-cho +, + +29.v.2000 + +, +E. Yamamoto +& +M. Doi +( +SPMN +) + +; + +2 males +, +1 female +, same locality, + +22.vi.2000 + +, +E. Yamamoto +& +M. Doi +( +SPMN +) + +; + +3 males +, +4 females +, same locality, + +29.vi.2000 + +, +E. Yamamoto +& +M. Doi +( +SPMN +) + +; + +3 females +, same locality, + +7.vii.2000 + +, +E. Yamamoto +& +M. Doi +( +SPMN +) + +; + +3 males +, +1 female +, same locality, + +15.vii.2000 + +, +E. Yamamoto +& +M. Doi +( +SPMN +) + +; + +2 males +, +1 female +, same locality, + +21.vii.2000 + +, +E. Yamamoto +& +M. Doi +( +SPMN +) + +; + +3 males +, +1 female +, +Oda-cho +, + +20.ix.2000 + +, +E. Yamamoto +( +SPMN +) + +. + + +Kochi + +: +1 pupa +(male), +Befu-kyo +, +Monobe-son +, +Kami-shi +, + +25.iv.2004 + +, +T +. +Hattori +( +SPMN +) + +; + +1 male +, +Nishikawa-keikoku +, +Umaji-mura +, + +24.iv.2004 + +, +K. Nio +( +SPMN +) + +; + +1 male +, +Uramasa-dani +, +Aki-shi +, + +25.iv.2004 + +, +K. Nio +( +SPMN +) + +; + +1 male +, +Shiraidani-keikoku +, +Hongawa +, +Ino-cho +, + +23.v.2002 + +, +K. Nio +( +SPMN +) + +; + +1 male +, same locality, + +1.vii.2005 + +, +M. Takai +( +SPMN +) + +; + +1 female +, +Teragawa +, +Hongawa +, +Ino-cho +, + +26.v.1999 + +, +A. Ohkawa +& +T +. +Ito +( +SPMN +) + +; + +1 female +, +Nagatani-keikoku +, +Sakawa-cho +, + +7.iv.2004 + +, +K. Nio +( +SPMN +) + +; + +1 male +(pinned), +Yahazu +, Higashi-tsuno-mura, + +10.x.1988 + +, +T +. +Nozaki +(NKa) + +; + +1 female +, +Irazuyama +, +Higashitsuno-mura +, + +8.v.2004 + +, +M. Takai +( +SPMN +) + +; + +1 male +, +Tsunoyama-kaitaku +, +Higashitsuno-mura +, + +8.v.2004 + +, +M. Takai +( +SPMN +) + +; + +2 males +, +Tengu-shinrinkôen +, +Higashitsuno-mura +, + +23.v.2004 + +, +M. Takai +( +SPMN +) + +. + + +Kyushu + +: + + + +Fukuoka + +: +1 male +, +Yoshii-machi +, +Ukiha-gun +, + +5.iv.1956 + +, +N. Gyotoku +( +KPM-NKMK12420 +) + +; + +1 male +, +Mishike +, +Imogawa +, +Ukiha-machi +, +Ukiha-shi +, + +13.v.1986 + +, +T +. +Nozaki + +; + +1 male +, +Dôbaru +, +Kokuraminami-ku +, +Kitakyushu-shi +, + +22.v.1996 + +, +T +. +Hattori +(in glycerin) ( +SPMN +) + +; + +1 male +, same locality, + +17.iv.2004 + +, +T +. +Hattori +( +SPMN +) + +; + +1 female +, same data (in glycerin) ( +SPMN +) + +; + +2 males +, +1 female +, +Uchigaso-keikoku +, +Hata +, +Nôgata-shi +, + +5.v.1997 + +, +T +. +Hattori +( +SPMN +) + +. + + +Kumamoto + +: +11 males +, +1 female +, +Kakizakoiwaoku +, +Izumi-mura +, + +24.v.1996 + +, +T +. +Hattori +( +SPMN +) + +; + +6 males +, same data (in glycerin) ( +SPMN +) + +; + +6 females +, same data (in glycerin) ( +SPMN +) + +. + + +Oita + +: +1 male +, +Shinyabakei +, +Yabakei-machi +, + +7.v.1997 + +, +T +. +Hattori +( +SPMN +) + +; + +1 female +, +Shimizubakuen +, +Mori +, +Kusu-machi +, + +18.iv.2004 + +, +T +. +Hattori +( +SPMN +) + +; + +2 males +, +Nakatsue-mura +, + +10.v.1997 + +, +H. Nishimoto +( +SPMN +) + +. + + +Miyazaki + +: +4 males +, +1 female +, +Torinosu-dani +, +Saigôyamasanga +, +Misato-cho +, + +27.v.2018 + +, +D. Nakano +(NKu) + +. + + +Kagoshima + +: +3 males +(pinned), +Natsunokawauchi +, +Kamou-machi +, +Aira-shi +, + +23.iii.1989 + +, +T +. +Nozaki +(NKa) + +; + +3 males +, +1 female +, +Kogihara +, +Ôkuchi-shi +, + +20–21.iv.2004 + +, +T +. +Hattori +( +SPMN +) + +. + + + + +Etymology. +The Latin species epithet + +“vesperalis + +” (= western) is an adjective referring to the broad distribution of this species in western +Japan +. + + + + +Distribution and biology. + +Rhyacphila vesperalis + +sp. nov. +is distributed in western Honshu, Shikoku and Kyushu ( +Fig. 9B +). Adults were collected near mountainous streams in April to September. + + +Japanese name. +Nishi-kuremensu-nagare-tobikera. + + + + +Remarks. +Although +Hattori (2005) +provided precise illustrations of the apical hinged process of the male segment X and the shape of the female segment VIII of specimens from western +Japan +and considered these to represent geographical variations of + +R. clemens + +( +Hattori 2005: 4 +d’ & 4e’ in Fig. 10), the examination of a large number of specimens in the present study revealed that the male and female genitalia illustrated by Hattori actually correspond to those of + +R. vesperalis + +sp. nov. +described above. The distributions of + +R. clemens + +and + +R. vesperalis + +sp. nov. +are allopatric except in +Okayama Prefecture +of western Honshu ( +Figs 9A, 9B +), but the differences between these two species in male and female genitalia are stable even in +Okayama Prefecture +. + + + + \ No newline at end of file diff --git a/data/38/55/87/385587AAF7371163FF4CC5DEFD5EA06C.xml b/data/38/55/87/385587AAF7371163FF4CC5DEFD5EA06C.xml new file mode 100644 index 00000000000..c78d330354d --- /dev/null +++ b/data/38/55/87/385587AAF7371163FF4CC5DEFD5EA06C.xml @@ -0,0 +1,3253 @@ + + + +Redescription of Rhyacophila clemens Tsuda 1940 (Trichoptera, Rhyacophilidae), with descriptions of five new, allied species from Japan + + + +Author + +Kawase, Naoki + +text + + +Zootaxa + + +2024 + +2024-05-03 + + +5447 + + +1 + + +55 +76 + + + + +http://dx.doi.org/10.11646/zootaxa.5447.1.3 + +journal article +10.11646/zootaxa.5447.1.3 +1175-5326 +11119209 +3A9842EC-F3D2-4839-9731-AA79A27B25CB + + + + + + + +Rhyacophila clemens +Tsuda 1940 + + + + + + + +( +Figs 1A–1J +, +2A–2K +, +9A +) + + + + + +Rhyacophila clemens +Tsuda 1940 + +, 124–125, male ( +Kyoto +, +Nagano +); +Tsuda 1948 +, 11–12, larva; +Ross 1956 +, 87, 118, male; +Schmid 1970 +, 95, 133, list; +Tani 1977 +, 198, male; +Tanida 1985 +, 186, larva; +Hattori 2005 +, 417, 423, 432, male, female, larva; +Inazu & Nishida 2011 +, 171, male, larva; +Nozaki 2016 +, 313, 314, male; +Hattori 2018 +, 477, 483, 492, male, female, larva. + + + + +Diagnosis. +The male of this species is distinguished from those of other Japanese species of the + +R. clemens + +Species Group by the combination of the following genitalic characters: The apical hinged process of segment X is Hshaped in ventral view ( +Figs 2B, 2C +1 +, +2C2 +), and the ventral plate of the aedeagus bears two or more small spines or protrusions posteromesally in ventral view ( +Figs 2B, 2D +1 +, +2D2 +). Regarding the female, + +R. clemens + +is similar to + +R. vesperalis + +sp. nov. +in having a round bulge on the dorsal margin of segment VIII in lateral view ( +Figs 2F, 2H1–2H +3 +), but + +R. vesperalis + +can be distinguished from the present species by bearing a pair of dorsolateral protrusions ( +Fig. 3G +). + + +Adult +( +Figs 1A–1D +). Length of each forewing: male +5.2–7.2 mm +(mean = 6.4, SD = 0.55, n = 62), female 6.0– +7.8 mm +(mean = 7.3, SD = 0.39, n = 19). Head dark brown, setal warts light brown with brown setae; antennae brown; palpi grayish brown. Thorax dark brown dorsally; pleurites light brown. Legs yellowish brown; spurs and spines grayish brown; tibiae and tarsi covered with brown pubescence. Abdomen with brown tergites, sternites yellowish brown. In fore- and hind wings, base color grayish brown; forewings bearing yellowish white speckles sparsely from base to apical margins, with larger spots on apical end of each cell ( +Fig. 1A +), and pale white markings on cross veins +r-m +, +m-cu +, and apical end of Cu2 vein; venation complete ( +Fig. 1D +), roots of fork I and fork II in each forewing approximately same length; discoidal and median cells open, thyridial cell (TC) closed; cross veins +r-m +and +m-cu +present. In abdomen, scent glands of sternite V open on antero-angle mounds well encircled by sutures; small mid ventral process on sternite VII in male, on sternite VI in female ( +Figs 2F, 2G +). + + +Male genitalia +( +Figs 1G–1J +, +2A–2E +). Segment IX (IX) wide trapezoidal in dorsal view, with round apicodorsal lobe (adl) ( +Fig. 2A +); dorsal half longer than ventral half in lateral view ( +Fig. 1G +). Preanal appendages absent. Segment X (X) reverse L-shaped in lateral view composed of vertical part (vp) and horizontal part (hp) ( +Fig. 1H +): vertical part tall in lateral view ( +Fig. 1H +); horizontal part widened, sub-rectangular in dorsal view, with posterior margin weakly bilobed ( +Fig. 2A +); apical hinged process (ahp) arising from horizontal part apicoventrally ( +Fig. 1G–1I +, +2A, 2B +), movable at base, H-shaped in ventral view, with pair of finger-like lobes directed posterodorsad, with pair of short mound-like extrusions directed anteroventrad ( +Figs. 2B, 2C +1 +, +2C2 +). Anal sclerites (as) composed of two pairs of lobes, each long rectangular in lateral view with common internal root ( +Fig. 1H +). Apical band (ab) well developed, semi-oval in lateral view, broadly surrounding anus and base of anal sclerites ( +Figs 1H, 1I +). Tergal band (tb) almost transparent but with some fine transverse folds, probably elastic ( +Figs 1H +, +2E +), connecting anteroventral part of apical band to dorsum of phallobase ( +Figs 1H, 1J +). Basal segment of each inferior appendage (bsia) elongate, gradually thickened posteriorly in lateral view ( +Fig. 1G +). Apical segment of each inferior appendage (asia) subtriangular in lateral view ( +Fig. 1G +), densely covered with fine hair-like setae mesally ( +Fig. 2A +). In phallic apparatus, phallobase (phb) short, cup-like ( +Figs 1H, 1J +); aedeagus (aed) forming narrow tube ( +Figs 1H, 1J +) with sclerotized ventral plate (vpl); ventral plate horizontal, tongue-shaped ( +Figs 1H–1J +) with longitudinal ridge dorsomesally, posterior margin with two or more small spines or protrusions posteromesally in ventral view ( +Figs 2B, 2D +1 +, +2D2 +). Parameres absent. + + + + +FIGURE 1. + +Rhyacophila clemens +Tsuda 1940 + +. + +1A–1J: 1A, male habitus, left dorsolateral (photographed by K. Inazu); 1B, male head and pro-, meso- and metanota, dorsal; 1C, male head, left lateral; 1D, male right wings, dorsal; 1E, lectotype (in glass tube) and labels preserved in INHS; 1F, male right wings, paralectotype (balsam mounted slide) preserved in OMNH; 1G–1J, male genitalia: 1G, left lateral; 1H, segment X and phallic apparatus, left lateral; 1I, same, posterodorsal; 1J, phallic apparatus, left dorsolateral. Abbreviations: I, II, III, IV, V = apical forks I, II, III, IV, V; IX, X = abdominal segments IX, X; A1, A2, A3 = anal veins 1–3; ab = apical band; aed = aedeagus; adl = apicodorsal lobe of segment IX; ahp = apical hinged process of segment X; as = anal sclerite; asia = apical segment of inferior appendage (paired); bsia = basal segment of inferior appendage (paired); C = costa; Cu1, Cu1a, Cu1b = cubital veins 1, 1a, 1b; hp = horizontal part of segment X; M1, M2, M3, M4 = median veins 1–4; +m-cu += crossvein between median and cubital veins; phb = phallobase; R1, R2, R3, R4, R5 = radial veins 1–5; +r-m += crossvein between radial and median veins; Sc = subcosta; tb = tergal band; TC = thyridial cell; vp = vertical part of segment X; vpl = ventral plate of aedeagus. + + + + + +FIGURE 2. + +Rhyacophila clemens +Tsuda 1940 + +. + +2A–2E, male genitalia: 2A, dorsal (left inferior appendage omitted); 2B, ventral (left inferior appendage and part of right inferior appendage omitted); 2C–2D, variations of apical hinged process of segment X, ventral (2C1, 2C2); variations of ventral plate of aedeagus, ventral (2D1, 2D2) (2C1, 2D1 collected from Hokkaido; 2C2, 2D2 from Ibaraki); 2E, apical band and tergal band, ventral; 2F–2K, female genitalia: 2F, left lateral; 2G, ventral; 2H1–2H3, variations of segment VIII, left lateral (2H1 collected from Hokkaido; 2H2, same Kanagawa; 2H3, same Nagano); 2I, segment VIII, ventral; 2J, vaginal apparatus, left lateral; 2K, same, ventral. Abbreviations: VI, VII, VIII, IX, X, XI = abdominal segments VI, VII, VIII, IX, X, XI; ab = apical band; adl = apicodorsal lobe of segment IX; as = anal sclerite; ahp = apical hinged process of segment X; asia = apical segment of inferior appendage (paired); bsia = basal segment of inferior appendage (paired); hp = horizontal part of segment X; phb = phallobase; pp = posterior process; ps = processus spermathecae; tb = tergal band; vp = vertical part of segment X; vpl = ventral plate of aedeagus; vr = ventral ridge (paired). Arrows see text. + + + +Female genitalia +( +Figs 2F–2K +). Segment VIII (VIII) annular, bearing dorsal bulge in lateral view (arrows indicated in +Figs 2F, 2H1–2H +3 +); with pair of ventral ridges (vr), forming longitudinal bridge, narrow anteriorly, slightly broader posteriorly in ventral view ( +Fig. 2I +); pair of apodemal rods reaching posterior end of segment VI ( +Fig. 2F +). Segment IX membranous, with pair of apodemal rods dorsolaterally extending into abdominal segment VI ( +Fig. 2F +). Vaginal apparatus simple; posterior process (pp) sclerotized, log shaped, long rectangular in lateral view ( +Fig. 2J +), long oval with pair of thin longitudinal wrinkles in ventral view ( +Fig. 2K +); processus spermathecae (ps) membranous ( +Figs 2J, 2K +). + + +Immature stage. +Larval stage has been described by +Tsuda (1948) +, +Tanida (1985) +, +Hattori (2005) +, and +Inazu & Nishida (2011) +. + + + + +Lectotype +. + +Male +(in alcohol, +Fig. 1E +, deposited in +INHS +) (present designation), labelled “Kumogahata, +Kyoto +/ + +7. vi.1936 + +, +Tsuda +leg.”, “ + +Rhyacophila +sp. + +No. 106/ +2♂ +2♀ +in copula”, “ + +Rhyacophila +/ + + +clemens +Ts. + +”, “ +INHS +Trichoptera +61337”, and “[ +Lectotype +] Male/ + +Rhyacophila clemens +Tsuda, 1940 + +/designated by +N. Kawase +, 2024”. + + + + + +Paralectotypes +. + +2 females +(in alcohol, deposited in +INHS +) + +, + +labelled “ +Kumogahata +, +Kyoto +/ + +7.vi.1936 + +, +Tsuda +leg.”, “ + +Rhyacophila +sp. + +No. +106/ +2♂ +2♀ +in copula”, “ + +Rhyacophila + +/ + +clemens +Ts. + +”, “ +INHS +Trichoptera +61337”, and “[ +Paralectotypes +] +2♀ +/ + +Rhyacophila clemens +Tsuda, 1940 + +/designated by +N. Kawase +, 2024” + +; + +3 males +(in alcohol, deposited in +INHS +) + +, + +labelled, “ +Chigonozawa +/ +Nagano +, +Japan +/ + +June 12, 1936 + +, Tsuda”, “ + +Rh. clemens + + +”, “ +INHS +Trichoptera +61336”, and “[ +Paralectotypes +] +3♂ +/ + +Rhyacophila clemens +Tsuda, 1940 + +/designated by +N. Kawase +, 2024” + +; + +1 male +(pinned, deposited in +CNC +) + +, + +labelled “ +Otakigawa-hontani +/ +Kiso +, +Nagano +, +Japan +/8-4-39 +Coll. Tsuda +”, “ + +Rhyacophila + + + + +clemens +Tsuda + +”, “ +CNC235664 +” and “ + +Rhyacophila clemens +Tsuda + +/ +Paralectotype + +/ +Designated N. Kawase +, 2024” + +; + +1 male +(same, in +CNC +) + +, + +labelled “ +Otakigawa-hontani +/ +Kiso +, +Nagano +, +Japan +/8-4-39/ +Tsuda +, +Coln. +”, “ +CNC1409475 +” and “ + +Rhyacophila clemens +Tsuda + +/ +Paralectotype + +/Designated by N. +Kawase +, 2024”; male right wings (preparation, +Fig. 1F +, deposited in +OMNH +), labeled “ + +Rhyacophila clemens + +n. sp. +”, “ + +Rhyacophila +No. + +106 ♂ +” + +. + + +Other specimens examined. + + +Hokkaido + +: +1 male +, +Jôzankei +, +Sapporo-shi +, + +30.vi.1974 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1male +, +1 female +, +Furubira-cho +, + +14.vi.1976 + +, +T + +. + +Hattori +( +SPMN +) + +; + +8 males +, +2 females +, +Kannon-zawa +, +Misumai +, +Sapporo-shi +, + +3.vii.1992 + +, +N. Kuhara +(NKu) + +; + +1 male +, +Shisamunai +, +Chitose-shi +, + +5.viii.2005 + +, +N. Kuhara +(NKu) + +; + +1 male +, same locality, + +3.viii.2012 + +, +N. Kuhara +(NKu) + +; + +3 males +, +1 female +, +Bifue +, +Chitose-shi +, + +30.vi.2006 + +, +T + +. + +Ito +& +T + +. + +Hattori +( +SPMN +) + +; + +2 males +, +2 females +, +Tarumae-gawa +, +Tomakomai-shi +, + +9.vi.1996 + +, +N. Kuhara +(NKu) + +; + +6 males +, +Shirai-sawa +, +Okusawasuigenchi +, +Otaru-shi +, + +29.vii.1996 + +, +Y. Sasaki +& +F. Takahashi +(NKa) + +; + +13 males +, +Chihase-gawa +, +Garô +, +Shimamakimura +, + +27.vii.2003 + +, +N. Kuhara +(NKu) + +; + +5 males +, +Ojironai-gawa +, +Himekawa +, +Mori-machi +, + +3–13.vii.1995 + +, +M. Nakajima +(NKa) + +; + +1 male +, +1 female +, +Shimazaki-gawa +, +Kasumi-dai +, +Mori-machi +, + +24.vi.2003 + +, +N. Kuhara +(NKa) + +; + +5 males +, +5 females +, +Iwafuchi-gawa +, +Kumaishi-cho +, + +27.vi–1.viii.1995 + +, +Y. Ito +& +T + +. + +Ito +(NKa) + +; + +10 males +, +4 females +, +Tatenosawa +, +Iwabe +, +Fukushima-cho +, + +21.vi.1995 + +, +N. Kuhara +(NKu) + +; + +3 males +, +2 females +, +Oyobe-gawa +, +Kamikawa +, +Matsumaecho +, + +3.vii.2005 + +, +N. Kuhara +(NKu) + +; + +3 males +, +Futami-cho +, +Hakodate-shi +, + +1.vi.2004 + +, +N. Kuhara +(NKu) + +; + +2 males +, +Ikusagawa +, +Nanae-cho +, + +23.vi.2003 + +, +N. Kuhara +(NKu) + +; + +2 males +, +Sakurano +, +Yakumo-cho +, + +1.vi.2004 + +, +N. Kuhara +(NKu) + +; + +1 male +, +1 female +, +Okusawa +, +Imakane-cho +, + +1.vii.2007 + +, +N. Kuhara +(NKu) + +; + +1 female +, +Saisago-gawa +, +Hayakawa +, +Kaminokuni-cho +, + +2.vii.2005 + +, +N. Kuhara +(NKa). + +Honshu + + +: + + +Aomori + +: +1 male +, +Okuse +, +Towada-shi +, + +14.vi.2004 + +, +N. Kuhara +(NKu) + +. + + +Iwate + +: +5 males +, +1 female +, +Ôkawame-cho +, +Kuji-shi +, + +12.vi.2004 + +, +N. Kuhara +(NKa) + +; + +1 male +, +Kadonameiri +, +Iwaizumi-cho +, + +12.vii.1997 + +, +N. Kuhara +(NKu) + +; + +2 males +, +Kadoma +, +Miyako-shi +, + +13.vii.1997 + +, +N. Kuhara +(NKu) + +; + +7 males +, +1 female +, +Kuzakai +, +Miyako-shi +, + +13.vii.1997 + +, +N. Kuhara +(NKu) + +; + +8 males +, +1 female +, +Naka-zawa +, +Kamikaai +, +Kitakami-shi +, + +2.vii.1995 + +, +T + +. + +Hattori +( +SPMN +) + +; + +5 males +, +Motouchi-gawa +, +Kitakami-shi +, + +20.vi.1997 + +, +T + +. + +Hattori +( +SPMN +) + +; + +2 males +, +1 female +, +Shitamae +, Nishi-waga-machi, + +13.vii.1997 + +, +N. Kuhara +(NKu) + +. + + +Miyagi + +: +1 male +, +Yokokawa +, +Shichikashuku-machi +, + +6.vii.1998 + +, +T + +. + +Hattori +( +SPMN +) + +. + + +Akita + +: +6 males +, +1 female +, +Asahi-gawa +, +Nibetsu +, +Akita-shi +, + +20.vi.1997 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1 male +(pinned), +Kotakizawa +, +Nakasen +, +Daisen-shi +, + +13.vi.2008 + +, +M. Tanaka +(MTa) + +; + +5 males +, +5 females +, +Akamizu-sawa +, +Sannai +, +Yokote-shi +, + +14.vii.1997 + +, +N. Kuhara +(NKa) + +. + + +Yamagata + +: +1 male +, +Oshôshizu +, +Yuza-machi +, + +9.vi.1998 + +, +H. Nishimoto +( +SPMN +) + +; + +4 males +, +Kinomezawa +, +Chôkai-san +, +Yuza-machi +, + +9.vi.1998 + +, +H. Nishimoto +( +SPMN +) + +; + +1 male +, +1 female +, +Kanjindai +, +Nagai-shi +, + +3.vii.1998 + +, +T + +. + +Hattori +( +SPMN +) + +; + +6 males +, +Hirokawara-gawa +, +Iide-machi +, + +3.vii.1998 + +, +T + +. + +Hattori +( +SPMN +) + +. + + +Fukushima + +: +10 males +, +Kurokawa +, +Shirakawa-shi, M +. +Kobayashi +( +KPM-NKMK 64270 +) + +. + + +Ibaraki + +: +4 males +, +Yonedaira +, +Nakadogawa +, +Takahagi-shi +, + +29.iv.1998 + +, +N. Kawase +(NKa) + +; + +2 males +, +Shôbusawa +, +Yasato +, +Ishioka-shi +, + +11–18.v.1997 + +, +N. Kawase +(NKa) + +; + +1 male +, +Obata +, +Yasato +, +Ishioka-shi +, + +13–20.v.1997 + +, +N. Kawase +(NKa) + +. + + +Tochigi + +: +1 male +, +Itamuro +, +Kuroiso +, +Nasushiobara-shi +, + +7.vi.1998 + +, +H. Nishimoto +( +SPMN +) + +; + +1 male +, +1 female +, +Nagai +, +Yaita-shi +, + +6.vi.1998 + +, +H. Nishimoto +( +SPMN +) + +; + +5 males +, +3 females +, +Shôjinzawa-yûsui +, +Yaita-shi +, + +7.vi.1998 + +, +H. Nishimoto +( +SPMN +) + +; + +1 male +, +Chûgûshi +, +Nikkô-shi +, + +6.vi.1998 + +, +H. Nishimoto +( +SPMN +) + +. + + +Tokyo + +: +1 male +, +1 female +(couple), +Kotosawa +, +Mitake +, +Oume-shi +, + +24.v.1989 + +, +T + +. + +Nozaki +(NKa) + +; + +35 males +, +9 females +, +Kitaaki-gawa +, +Koiwa +, +Hinohara-mura +, + +14.vi.1989 + +, +T + +. + +Nozaki +(NKa) + +. + + +Kanagawa + +: +21 males +, +5 females +, +Nishizawa +, +Nakagawa +, +Yamakita-machi +, + +8.vi.2020 + +, +T + +. + +Nozaki +(NKa) + +; + +1 male +, same locality, + +28.iv.2023 + +, +T + +. + +Nozaki +(NKa) + +. + + +Niigata + +: +5 males +, +2 females +, +Sasagawa +, +Sado-shi +, + +12.v.1985 + +, +K. Baba +( +KPM-NKMK 84910 +) + +; + +3 males +, +Imagawa +, +Murakami-shi +, + +24.vi.1956 + +, +K. Baba +( +KPM-NKMK 17780 +) + +; + +1 male +, +Budo +, +Murakami-shi +, + +27.vi.1964 + +, +K. Baba +( +KPM-NKMK 18800 +) + +; + +1 male +, same data, +K. Baba +( +KPM-NKMK 18850 +) + +; + +1 male +, +Sanpokumachi +, +Murakami-shi +, + +25.ix.1968 + +, +M. Kobayashi +( +KPM-NKMK 22270 +) + +; + +1 male +, +Kurokawa-mura +, +Tainai-shi +, + +11.vii.1964 + +, +K. Baba +( +KPM-NKMK 19510 +) + +; + +2 males +, +1 female +, same locality, + +15.vii.1964 + +, +K. Baba +( +KPM-NKMK 19560 +) + +; + +1 male +, +2 females +, +Ginzan-daira +, +Yunotani-mura +, + +2.vii.1999 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1 female +, +Matsunoyamamatsukuchi +, +Tôkamachi-shi +, + +24.vi–2.vii.2021 + +, +D. Kato +(NKa) + +; + +1 male +, +Wasabi-zawa +, +Ôdokoro +, +Itoigawa-shi +, + +14.viii.1998 + +, +T + +. + +Hattori +( +SPMN +) + +; + +3 males +, +Irikon-zawa +, +Itoigawa-shi +, + +16.viii.1996 + +, +T + +. + +Hattori +( +SPMN +) + +. + + +Toyama + +: +1 male +, +Sakai-gawa +, +Yamazaki +, +Asahi-machi +, + +23.ix.2004 + +, +N. Kuhara +(NKu) + +. + + +Fukui + +: +3 males +, +Ichijyôdani +, +Fukui-shi +, + +30.iv.1998 + +, +H. Nishimoto +( +SPMN +) + +; + +6 males +, +2 females +, +Okuasô +, +Tsuruga-shi +, + +19.vi.1994 + +, +T + +. + +Hattori +( +SPMN +) + +. + + +Nagano + +: +6 males +, +Chigono-sawa +, +Kisofukushima-machi +, + +13.vi.1998 + +, +T + +. + +Hattori +( +SPMN +) + +; + +5 males +, same data (in glycerin) ( +SPMN +) + +; + +2 females +, same data (in glycerin) ( +SPMN +) + +. + + +Gifu + +: +1 female +, +Iwaimachi +, +Takayama-shi +, + +9.vi.2003 + +, +H. Nishimoto +( +SPMN +) + +; + +7 males +, +1 female +, +Namai +, +Taki-machi +, +Takayama-shi +, + +7.vi.2003 + +, +H. Nishimoto +( +SPMN +) + +; + +18 males +, +3 females +, same locality, + +24.vi.2004 + +, +H. Nishimoto +( +SPMN +) + +; + +14 males +, +2 females +, same locality, + +18.vi.2005 + +, +H. Nishimoto +( +SPMN +) + +; + +2 females +, +Tsukechi-kyo +, +Shimoure +, +Tsukechi-cho +, + +13.v.2002 + +, +H. Nishimoto +( +SPMN +) + +; + +4 males +, +1 female +, +Enbara +, +Miyama-cho +, +Yamagata-shi +, + +5.v.1996 + +, +T + +. + +Hattori +( +SPMN +) + +; + +12 males +, +Nishimaenotani +, +Tsurumi +, +Ibigawa-cho +, + +28–29.v.2002 + +N. Kawase +(NKa) + +; + +3 males +, +Ozu +, +Kuze +, +Ibigawa-cho +, + +25.v.2002 + +, +N. Kawase +(NKa) + +; + +2 males +, +2 females +, +Kuze +, +Ibigawa-cho +, + +27.v.2004 + +, +H. Nishimoto +( +SPMN +) + +; + +2 males +, +1 female +, +Sakauchigawa +, +Sakauchi-kawakami +, +Ibigawa-cho +, + +7.vi.1998 + +, +T + +. + +Hattori +( +SPMN +) + +; + +4 males +, +4 females +, +Hassô-gawa +, +Sakauchi-kawakami +, +Ibigawa-cho +, + +7.vi.1998 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1 male +, +Sakauchi-sakamoto +, +Ibigawa-cho +, + +1.vi.2022 + +, +N. Kawase +(NKa) + +. + + +Shizuoka + +: +1 male +, +Funabara-gawa +, +Izu-shi +, + +18.v.1996 + +, +T + +. + +Hattori +(in glycerin) ( +SPMN +) + +; + +1 male +, +1 female +, same locality, + +16.vi.1996 + +, +T + +. + +Hattori +( +SPMN +) + +; + +4 males +, +1 female +, +Kamifunabara +, +Izu-shi +, + +1.iv.2009 + +, +T + +. + +Hattori +& +T + +. + +Ito +( +SPMN +) + +; + +1 male +, +Kazehaya-toge +, +Izu-shi +, + +3.vi.2009 + +, +T + +. + +Hattori +& +T + +. + +Ito +( +SPMN +) + +; + +1 female +, +Ôsouri +, +Nishiizucho +, + +3.vi.2009 + +, +T + +. + +Hattori +& +T + +. + +Ito +( +SPMN +) + +; + +6 males +, +5 females +, +Momosawa-gawa +, +Nagaizumi-cho +, +Numazu-shi +, + +8.iv.1995 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1 female +, +Nagao-gawa +, +Hirayama +, +Shizuoka-shi +, + +27.iv.2006 + +, +T + +. + +Hattori +( +SPMN +) + +: + +9 males +, +1 female +, same locality, + +8.vi.2006 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1 male +, +Hikage-sawa +, +Umegashima +, +Shizuoka-shi +, + +21.vi.2002 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1 male +, +Minami-sawa +, +Umegashima +, +Shizuoka-shi +, + +28.vi.1997 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1 male +, +1 female +, +Kurobe-sawa +, +Hirano +, +Shizuoka-shi +, + +1.vi.1997 + +, +T + +. + +Hattori +( +SPMN +) + +; + +3 males +, +2 females +, same locality, + +10.vii.1999 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1 female +, +Yokosawa +, +Shizuoka-shi +, + +5.vi.1999 + +, +T + +. + +Hattori +( +SPMN +) + +; + +2 males +, +6 females +, same locality, + +9.vi.2001 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1 male +, +1 female +, same locality, + +3.v.2002 + +, +T + +. + +Hattori +( +SPMN +) + +; + +2 males +, same locality, + +21.v.2003 + +, +T + +. + +Hattori +( +SPMN +) + +; + +3 males +, same locality, + +21.vi.2003 + +, +T + +. + +Hattori +( +SPMN +) + +; + +5 males +, +Shiraisizawa +, +Takumi +, +Shizuoka-shi +, + +28.v.2001 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1 male +, +1 female +, +Yuyama +, +Shizuoka-shi +, + +29.iv.1997 + +, +T + +. + +Hattori +( +SPMN +) + +; + +8 males +, +2 females +, +Warashina-gawa +, +Yunoshima +, +Shizuoka-shi +, + +11.v.2001 + +, +T + +. + +Hattori +( +SPMN +) + +. + + +Mie + +: +3 males +, +Inabe-gawa +, +Fujiwara-cho +, +Inabe-shi +, + +21.iii.2001 + +, +F. Nishimoto +( +SPMN +) + +; + +17 males +, +4 females +, +Yamaguchi +, +Fujiwara-cho +, +Inabe-shi +, + +4.vi.2006 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1 male +, +Sakashita +, +Kameyama-shi +, + +9.vi.2006 + +, +N. Kawase +(NKa) + +; + +1 male +, +Kamitage +, +Misugi-cho +, + +14.vi.2009 + +, +H. Morita +(NKa) + +; + +13 males +, +Hachisugawa +, +Iitaka-cho +, + +27.v.2004 + +, +T + +. + +Hattori +( +SPMN +) + +. + + +Shiga + +: +4 males +, +Harikawa +, +Yogo-cho +, +Nagahama-shi +, + +1.vi.2009 + +, +N. Kawase +(NKa) + +; + +3 males +, +2 females +, +Samukaze-gawa +, +Imazu-cho +, +Takashima-shi +, + +19.v.1988 + +, +K. Tanida +( +OMNH +) + +; + +7 males +, +Kimigahata +, +Eigenji +, Higashi-ômi-shi, + +16.v.1993 + +, +K. Tanida +( +OMNH +) + +; + +1 male +, +Shirakura-dani +, +Ôkawara +, +Tsuchiyama-cho +, +Koka-shi +, + +17.v.2005 + +, +N. Kawase +(NKa) + +; + +1 male +, same locality, + +10.viii.2008 + +, +N. Kawase +( +LBM1410012584 +) + +; + +7 males +, +Ômiya-gawa +, +Sakamoto-honmachi +, +Ôtsu-shi +, + +31.v.1987 + +, +K. Tanida +( +OMNH +) + +; + +4 males +, +2 females +, +Hiyoshi-taisha +, +Sakamoto +, +Ôtsu-shi +, + +24.v.1981 + +, +K. Tanida +( +OMNH +) + +; + +1 male +, same locality, + +3.v.1987 + +, +K. Tanida +( +OMNH +) + +. + + +Kyoto + +: +1 male +, +Kurama +, +Kyoto-shi +, + +19.v.1974 + +, +T + +. + +Hattori +(in glycerin) ( +SPMN +) + +; + +1 female +, same data (in glycerin) ( +SPMN +) + +; + +14 males +, +1 female +, +Oku-miya +, +Kibune +, +Kyoto-shi +, + +30.v.1987 + +, +K. Tanida +( +OMNH +) + +; + +2 males +, +2 females +(2 couples), same data, +K. Tanida +( +OMNH +) + +. + + +Osaka + +: +3 males +, +1 female +, +Takihata +, Kawachi-nagano-shi, + +10.iv.1990 + +, +K. Tanida +( +OMNH +) + +; + +1 male +, +1 female +, same locality, + +15.v.1984 + +, +Nishida +( +SPMN +) + +; + +1 male +, +1 female +, same locality, + +15.v.1984 + +, +H. Nishimoto +( +SPMN +) + +; + +2 males +, +1 female +, same locality, + +17.v.1985 + +, +H. Nishimoto +( +SPMN +) + +; + +1 male +, Izumi-Katsuragi-san, +Kisihwada-shi +, + +22.v.1984 + +, +H. Nishimoto +( +SPMN +) + +. + + +Hyogo + +: +1 male +, +1 female +, +Amago-ike +, +Takenouchi +, +Wadayama-cho +, +Asago-shi +, + +7.v.2002 + +, +K. Inazu +( +SPMN +) + +; + +1 male +, +1 female +, same locality, + +1.vi.2004 + +, +K. Inazu +(NKa) + +; + +1 male +, +1 female +, same locality, + +4.vi.2004 + +, +K. Inazu +( +LBM1410012585–1410012586 + +; + +2 males +, +Kirigataki +, Shin-onsen-cho, no collecting date, +K. Inazu +( +SPMN +) + +; + +4 males +, +Ojiro +, +Mikata +, +Kami-cho +, + +21.vi– 11.vii.2015 + +, +S. Fujie +( +OMNH +) + +. + + +Nara + +: +1 male +, +Ômataguchi +, Higashi-yoshino-mura, + +29.v.1988 + +, +K. Tanida +( +OMNH +) + +; + +3 males +, +Takahara +, +Kawakami-mura +, + +27.v.2004 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1 male +, +Sanjyô-gawa +, +Tenkawa-mura +, + +15.v.2004 + +, +T + +. + +Hattori +( +SPMN +) + +. + + +Wakayama + +: +1 male +, +Uigoke +, +Kanaya +, +Aritagawa-cho +, + +26.iv.2004 + +, +T + +. + +Hattori +( +SPMN +) + +; + +2 males +, Takiwake-no-taki, +Takata +, +Shingû-shi +, + +20.v.1990 + +, +N. Kuhara +(NKu) + +. + + +Okayama + +: +2 males +, +2 females +, +Kamisaibaraendô +, +Kagamino-cho +, + +14.viii.2011 + +, +K. Nojima +(NKa) + +; + +2 males +, +Shiraka-keikoku +, +Tomi-nishidani +, +Kagamino-cho +, + +26.vi.2016 + +, +K. Nojima +(NKa) + +; + +2 males +, +Ôgaya +, Nishi-awakura-son, + +12.v.2016 + +, +K. Nojima +(NKa) + +; + +3 males +, same locality, + +20.vii.2016 + +, +K. Nojima +( +LBM1410012587–1410012589 +) + +; + +2 males +, +Hiruzen-kamifukuda +, +Maniwa-shi +, + +5.v.2016 + +, +K. Nojima +(NKa) + +. + + + + +Remarks +. +Tsuda (1940) +described this species based on +34 males +and +16 females +collected from several localities in Kyoto and Nagano Prefectures (central Honshu), but he did not designate the +holotype +. The collection of the late Matsunae Tsuda was believed to have been mostly lost except for microscopic preparations of wings of some species (Tanida personal communication 2023). For this species, only the right wings of a male that was definitely used by +Tsuda (1940) +are deposited in the Osaka Museum of Natural History (OMNH) ( +Fig. 1F +). Although the shape, coloration, and venation of the wings agree well with those of + +R. clemens + +described above, they are insufficient for confirming species identity. However, through the course of my study, I noticed that several specimens of + +R. clemens + +used by +Tsuda (1940) +are presently deposited in the Herbert H. Ross collection of the +Illinois +Natural History Survey in the +USA +(https://www.gbif.org/occurrence/search?dataset_key=68513375-3aa5- 4f6f-9975-d97d56c21d61&taxon_key=5053001) ( +Fig. 1E +). The collection data of these specimens ( +4 males +and +2 females +) agree with some of the specimens in the specimen list of +Tsuda (1940) +and Tsuda’s species number “ + +Rhyacophila +sp. + +No. 106” labeled in the vial of “INHS +Trichoptera +61337” ( +Fig. 1E +) corresponds to the number “ + +Rhyacophila +No. + +106” on the male wing preparation in OMNH ( +Fig. 1F +). These specimens must be some of the +syntypes +of this species. Furthermore, I found that two pinned male specimens of + +R. clemens + +deposited in the Canadian National Collection of Insects, Arachnids & Nematodes in +Canada +(https://www.cnc.agr.gc.ca/taxonomy/ Specimen.php?id=235664; https://www.cnc.agr.gc.ca/taxonomy/Specimen.php?id=2072494) were also used in the original description. + + +I examined +four male +and +two female +specimens (“ +INHS +Trichoptera +61336 & 61337”) and photographs of male genitalia (“ +CNC 235664 +”) kindly provided by +Tommy McElrath +( +INHS +) and +Owen Lonsdale +( +CNC +), respectively. +The +genital morphology of these agreed well with that of + +R. clemens + +described above. +In +order to promote nomenclatural stability and facilitate further identifications of this species, I choose a male in the +INHS +collection, preserved in ethyl alcohol in a glass vial, as the +lectotype +with the following five labels: “Kumogahata, +Kyoto +; + +7.VI.1936 + +. +Tsuda +leg.// + +Rhyacophila +sp + +No. 106; +2♂ +2♀ +in copula// + +Rhyacophila clemens +Ts. + +// +INHS +; +Trichoptera +; 61337//[ +Lectotype +] Male; + +Rhyacophila clemens +Tsuda, 1940 + +; designated by +N. Kawase +, 2024” with the first three labels in Tsuda’s handwriting and the last two labels printed ( +Fig. 1E +). + + +This species was also recorded from Iriomote-jima, Ryukyu Archipelago ( +Kuranishi 1997 +) and from +Taiwan +( +Kiss 2013 +; +Malicky 2014 +), but I could not examine the specimens used in these studies. Reexamination of these records is necessary since + +R. clemens + +was not found from Shikoku and Kyushu, southwestern +Japan +in the present study ( +Fig. 9A +). + + + + +Distribution and biology. + +Rhyacophila clemens + +is one of the common + +Rhyacophila +species + +of +Japan +and is broadly distributed from southwestern +Hokkaido +to western Honshu ( +Fig. 9A +). Adults are collected near mountain streams in late April to September. +Taira (2023) +indicated that this species has a univoltine life cycle. + + +Japanese name +. Kuremensu-nagare-tobikera. + + + + \ No newline at end of file diff --git a/data/38/55/87/385587AAF7381175FF4CC443FC9CA705.xml b/data/38/55/87/385587AAF7381175FF4CC443FC9CA705.xml new file mode 100644 index 00000000000..6a8f715d384 --- /dev/null +++ b/data/38/55/87/385587AAF7381175FF4CC443FC9CA705.xml @@ -0,0 +1,426 @@ + + + +Redescription of Rhyacophila clemens Tsuda 1940 (Trichoptera, Rhyacophilidae), with descriptions of five new, allied species from Japan + + + +Author + +Kawase, Naoki + +text + + +Zootaxa + + +2024 + +2024-05-03 + + +5447 + + +1 + + +55 +76 + + + + +http://dx.doi.org/10.11646/zootaxa.5447.1.3 + +journal article +10.11646/zootaxa.5447.1.3 +1175-5326 +11119209 +3A9842EC-F3D2-4839-9731-AA79A27B25CB + + + + + + + +Rhyacophila parvicauda + +sp. nov. + + + + + + +( +Figs 6A–6H +, +9D +) + + + + +Diagnosis +. The male of + +R. parvicauda + +sp. nov. +is similar to those of + +R. inazui + +sp. nov. +and + +R angulicauda + +sp. nov. +in having a U-shaped apical hinged process of segment X in ventral view, but can be distinguished from the latter two by the shape of the apicodorsal lobe of segment IX given in the diagnosis for + +R. inazui + +sp. nov. +Additionally, the male genitalia of this species are unique among this species group in having rows of dense spine-like setae along the mesodorsal margin of the apical segment of each inferior appendage ( +Figs 6A, 6C +). Moreover, the apical hinged process of this species is clearly shorter than the other two species, only 1/2 as long as the horizontal part of segment X ( +Fig. 6A +), but those of the other two species are about as long as the horizontal part ( +Figs 4C +, +5A +). Regarding the female, + +R. parvicauda + +sp. nov. +is similar to + +R. furcicauda + +sp. nov. +in having many brown thick setae on the lateral surface of segment VIII ( +Fig. 6E +), but can be distinguished from the latter by the shape of ventral ridges: In + +P. +parvicauda + +sp. nov. +, a ventral ridge of segment VIII is visible posteriorly from the side (arrow in +Fig. 6E +), but in + +P. +furcicauda + +sp. nov. +, the ventral ridge is invisible in lateral view ( +Fig. 7G +). + + +Adult +. Length of each forewing: male +6.4–7.3 mm +(mean = 6.7, SD = 0.32, n = 7), female +6.2–6.9 mm +(mean = 6.6, n = 2). General morphology and coloration similar to those of + +R. clemens + +, but wing venation similar to that of + +R. inazui + +sp. nov. +( +Fig. 4B +), root of fork I on each forewing clearly longer than that of fork II. + + +Male genitalia +( +Figs 6A–6D +). Segment IX dorsal half longer than ventral half in lateral view ( +Fig. 6A +), wide rectangular in dorsal view with small apicodorsal lobe ( +Fig. 6C +). Preanal appendages absent. Segment X reverse L-shaped in lateral view, composed of vertical part and horizontal part: vertical part tall in lateral view ( +Fig. 6B +); horizontal part thick, oval in dorsal view ( +Fig. 6C +); apical hinged process U-shaped in ventral view, with pair of short finger-like lobes parallel, 1/2 as long as horizontal part in lateral view, lobes apically rounded, directed posterodorsad ( +Figs 6A–6D +). Anal sclerites composed of two pairs of lobes, each long and rectangular in lateral view, with common internal root ( +Figs 6B, 6D +). Apical band well developed, semi-oval in lateral view, broadly surrounding anus and root of anal sclerites ( +Figs 6B, 6D +). Tergal band connecting ventral part of apical band to dorsum of phallobase ( +Fig. 6B +). Basal segment of each inferior appendage setose, elongate, basal 1/3 narrowest in lateral view ( +Fig. 6A +). Apical segment of each inferior appendage subtriangular in lateral view ( +Fig. 6A +); mesal surface densely covered by long fine setae, with rows of spine-like setae along dorsal margin ( +Fig. 6C +). In phallic apparatus, phallobase short ( +Fig. 6B +); aedeagus narrow tube with sclerotized ventral plate ( +Fig. 6B +); ventral plate horizontal, tongue-shaped with posterior margin truncate in ventral view ( +Fig. 6D +). Parameres absent. + + +Female genitalia +( +Figs 6E–6H +). Segment VIII annular, dorsal margin almost straight or slightly concave in lateral view ( +Fig. 6E +); pair of ventral ridges widely separated, posterior ends curved posterodosad, visible in lateral view ( +Figs 6E, 6F +); many brown thick setae on lateral surface ( +Figs 6E, 6F +); pair of apodemal rods reaching to posterior end of segment VI. Segment IX membranous, with pair of apodemal rods dorsolaterally, extending into abdominal segment VI. Vaginal apparatus simple; posterior process sclerotized, dorsal margin round in lateral view ( +Fig. 6G +), apparatus long-oval in ventral view ( +Fig. 6H +); processus spermathecae membranous. + + + + +FIGURE 6. + +Rhyacophila parvicauda + +sp. nov. + +6A–6D, male genitalia: 6A, left lateral; 6B, segment X and phallic apparatus, left lateral; 6C, dorsal (left inferior appendage omitted); 6D, ventral (left inferior appendage omitted). 6E–6H, female genitalia: 6E, segment VIII, left lateral; 6F, same, ventral; 6G, vaginal apparatus, left lateral; 6H, same, ventral. Abbreviation: vr = ventral ridge. Arrows see text. + + + +Immature stage +. Unknown. + + + + + + +Holotype +. + +Male +(in alcohol), +Mt. Koya-yama +primary forests, +Oda-cho +, +Ehime Prefecture +, +Shikoku +, +Japan +, +33°30’27”N +132°51’39”E +, alt. + +1100 m + +, + +29.vi.2000 + +, +E. Yamamoto +( +LBM1410012649 +). + + + + + +Paratypes +. +Shikoku +: +Ehime + + +: + +2 males +, +1 female +, same locality as the holotype, + +7.vii.2000 + +, +E. Yamamoto +& +M. Doi +( +LBM1410012650–1410012652 +) + +; + +1 male +, +1 female +, same locality as the holotype, + +15.vii.2000 + +, +E. Yamamoto +& +M. Doi +(SPMN-IS-59791–59795) + +; + +3 males +, same locality as the holotype, + +21.vii.2000 + +, +E. Yamamoto +& +M. Doi +(SPMN-IS-59788–59790) + +; + +4 males +, same locality as the holotype, + +29.vii.2000 + +, +E. Yamamoto +& +M. Doi +(SPMN-IS-59796–59799) + +; +1 male +, Oda-miyama. Oda-cho, +31.v.2001 +, E. Yamamoto (SPMN-IS-59786); + +1 male +, same locality, + +10.vi.2001 + +, +E. Yamamoto +(SPMN-IS-59787) + +. + + + + +Other specimens examined +. +Shikoku +: +Ehime + +: +1 male +, same locality as the holotype, + +19.viii.2000 + +, +E. Yamamoto +& +M. Doi +( +SPMN +) + +; + +1 female +, same locality as the holotype, + +20.ix.2000 + +, +E. Yamamoto +( +SPMN +) + +. + + +Kochi + +: +1 male +, +1 female +, Setogawakeikoku, Tosa-cho, Tosa-gun, + +27.v.2004 + +, +K. Nio +( +SPMN +) + +. + + + + +Etymology. +The species name + +“parvicauda + +” (= short tail) is a noun in apposition referring to the short, apical, hinged process of segment X. + + + + +Distribution and biology. + +Rhyacophila parvicauda + +sp. nov. +was collected only from a few small headwater streams in a mountain area of Shikoku ( +Fig. 9D +). This species tends to be distributed at rather higher altitude than + +R. inazui + +and + +R. vesperalis + +in the same river systems. Adults of this species were collected from late May to August. + + +Japanese name. +Hime-kuremensu-nagare-tobikera. + + + + \ No newline at end of file diff --git a/data/38/55/87/385587AAF73A116BFF4CC6A3FD04A4D4.xml b/data/38/55/87/385587AAF73A116BFF4CC6A3FD04A4D4.xml new file mode 100644 index 00000000000..1fec0e249fe --- /dev/null +++ b/data/38/55/87/385587AAF73A116BFF4CC6A3FD04A4D4.xml @@ -0,0 +1,993 @@ + + + +Redescription of Rhyacophila clemens Tsuda 1940 (Trichoptera, Rhyacophilidae), with descriptions of five new, allied species from Japan + + + +Author + +Kawase, Naoki + +text + + +Zootaxa + + +2024 + +2024-05-03 + + +5447 + + +1 + + +55 +76 + + + + +http://dx.doi.org/10.11646/zootaxa.5447.1.3 + +journal article +10.11646/zootaxa.5447.1.3 +1175-5326 +11119209 +3A9842EC-F3D2-4839-9731-AA79A27B25CB + + + + + + + +Rhyacophila angulicauda + +sp. nov. + + + + + + +( +Figs 5A–5I +, +9D +) + + + + +Diagnosis +. The male of + +R. angulicauda + +sp. nov. +is very similar to those of + +R. inazui + +sp. nov. +and + +R parvicauda + +sp. nov. +in having a U-shaped apical hinged process of segment X in ventral view, but can be easily distinguished from the latter two species by the shape of the apicodorsal lobe of segment IX given in the diagnosis for + +R. inazui + +sp. nov. +The female of + +R. angulicauda + +is similar to those of + +R. inazui + +sp. nov. +, + +R. parvicauda + +sp. nov. +, and + +P. +furcicauda + +sp. nov. +in having an almost straight dorsal margin of segment VIII in lateral view, but can be distinguished from the latter three by the characters of segment VIII as indicated in the diagnosis for + +R. inazui + +sp. nov. + + +Adult +. Length of each forewing: male 6.0– +7.6 mm +(mean = 6.8, SD = 0.46, n = 27), female +6.9–9.1 mm +(mean = 8.0, SD = 0.54, n = 13). General morphology and coloration similar to those of + +R. clemens + +. In venation, this species also similar to + +R. clemens + +( +Fig. 1D +), root of fork I and II of each forewing approximately same length each other. + + +Male genitalia +( +Figs 5A–5D +). Segment IX dorsal half longer than ventral half in lateral view ( +Fig. 5A +), trapezoidal in dorsal view; apicodorsal lobe trapezoidal in dorsal view, angular in lateral view, strongly overhanging segment X ( +Figs 5A, 5C +). Preanal appendages absent. Segment X reverse L-shaped in lateral view composed of vertical part and horizontal part: vertical part tall in lateral view ( +Fig. 5B +); horizontal part nearly oval and slightly bilobed posteriorly in dorsal view ( +Fig. 5C +); apical hinged process U-shaped in ventral view, with pair of thick finger-like lobes parallel to each other, each apex round, directed posterodorsad ( +Figs 5B–5D +); pair of anteroventral corners (of ahp) round, forming sub-oval mounds ( +Fig. 5D +). Anal sclerites composed of two pairs of lobes, each long rectangular in lateral view, with common internal root ( +Figs 5B, 5D +). Apical band well developed, subtriangular with round corners in lateral view, broadly surrounding anus and root of anal sclerites ( +Figs 5B, 5D +). Tergal band connecting base of apical band to dorsum of phallobase ( +Fig. 5B +). Basal segment of each inferior appendage setose, elongate, posterior half gradually thicker in lateral view ( +Fig. 5A +). Apical segment of each inferior appendage subtriangular in lateral view ( +Fig. 5A +), covered with fine setae mesally ( +Fig. 5C +). In phallic apparatus, phallobase short, cup like ( +Fig. 5B +); aedeagus forming narrow tube with sclerotized ventral plate ( +Figs 5B, 5D +); ventral plate horizontal and tongue-shaped with posterior margin truncated or shallowly concave in ventral view ( +Fig. 5D +). Parameres absent. + + +Female genitalia +( +Figs 5E–5I +). Segment VIII annular, dorsal margin almost straight in lateral view ( +Figs 5E, 5F +); with pair of ventral ridges forming longitudinal narrow bridge, narrowest in anterior 1/4–1/ +3 in +ventral view ( +Fig. 5G +); pair of apodemal rods extending into segment VI ( +Fig. 5E +). Segment IX membranous, with pair of apodemal rods dorsolaterally, extending into abdominal segment VI. Vaginal apparatus simple; posterior process sclerotized, jackknife-shaped, dorsal margin slightly convex in lateral view ( +Fig. 5H +), long oval in ventral view ( +Fig. 5I +); processus spermathecae membranous ( +Figs 5H, 5I +). + + +Immature stage +. Unknown. + + + + + + +Holotype +. + +Male +(in alcohol), +Abe-tôge +(alt. + +1400 m + +), +Umegashima +, +Shizuoka-shi +, +Shizuoka Pref. +, +Honshu +, +Japan +, 35°18’46”–55”N 138°21’4”–19”E, alt. 1400 m, + +21.vi.2007 + +, +T +. Hattori ( +LBM1410012630 +). + + + + + +Paratypes +. +Honshu +: +Kanagawa + + +: + +9 males +, +3 females +, +Nishizawa +, +Nakagawa +, +Yamakita-machi +, + +27.v.2020 + +, +T +. +Nozaki +( +LBM1410012637–1410012648 +) + +; + +3 males +, +1 female +, same locality, + +28.iv.2023 + +, +T +. +Nozaki +( +OMNH +). + +Shizuoka + + +: + +2 males +, same data as the holotype (SPMN-IS-59778–59779) + +; + +1 male +, +1 female +, same locality as the holotype, + +21.vii.1997 + +, +T +. +Hattori +(SPMN-IS-59755–59756) + +; + +2 males +, +4 females +, same locality as the holotype, + +6.vi.1999 + +, +T +. +Hattori +( +LBM1410012631–1410012636 +) + +; + +2 males +, +1 female +, same locality as the holotype, + +10.vii.1999 + +, +T +. +Hattori +(SPMN-IS-59780–59782) + +; + +2 males +, same locality as the holotype, + +14.vii.2001 + +, +T +. +Hattori +(SPMN-IS-59757–59758) + +; + +2 males +, +1 female +, +Nishi-hikagesawa +, +Umegashima +, +Shizuoka-shi +, + +28.v.2014 + +, +T +. hattori & +T +. +Nozaki +(SPMN-IS-59783–59785) + +; + +12 males +, +7 females +, +Minami-sawa +, +Umegashima +, +Shizuoka-shi +, + +2.vi.1996 + +, +T +. +Hattori +(SPMN-IS-59759–59777) + +. + + + + +FIGURE 5. + +Rhyacophila angulicauda + +sp. nov. + +5A–5D, male genitalia: 5A, left lateral; 5B, segment X and phallic apparatus, left lateral; 5C, dorsal (left inferior appendage omitted); 5D, ventral (left inferior appendage and apex of apical segment of right inferior appendage omitted). 5E–5I, female genitalia: 5E, left lateral; 5F, segment VIII, left lateral; 5G, same, ventral; 5H, vaginal apparatus, left lateral; 5I, same, ventral. Arrows see text. + + + +Other specimens examined. Honshu: + + +Tokyo + +: +4 males +, +Nippara-gawa +, +Okutama-machi +, + +5.vi.1991 + +, +T + +. + +Kagaya +& +T + +. + +Nozaki +(NKa) + +. + + +Kanagawa + +: +4 males +, +Sokozawa +, +Sagamihara-shi +, + +9.iv.1984 + +, +T + +. + +Nozaki +(NKa) + +; + +5 males +, +Shiomizu-gawa +, +Kiyokawa-mura +, + +5.vi.1994 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1 female +, +Shiraishizawa +, +Yamakita-machi +, + +26.iv.1984 + +, +T + +. + +Nozaki + +; + +1 female +, same locality, + +2–3.vi.1984 + +, +T + +. + +Nozaki +(NKa) + +; + +25 males +, +5 females +, +Nishizawa +, +Nakagawa +, +Yamakita-machi +, + +8.vi.2020 + +, +T + +. + +Nozaki +(NKa) + +. + + +Niigata + +: +7 males +, +1 female +, +Wasabi-zawa +, +Ôdokoro +, +Itoigawa-shi +, + +14.viii.1998 + +, +T + +. + +Hattori +( +SPMN +) + +. + + +Yamanashi + +: +1 male +, +1 female +, Doryu-no-taki, +Nishi-ide +, +Ôizumicho +, +Hokuto-shi +, + +30.v.1997 + +, +T + +. + +Hattori +( +SPMN +) + +; + +7 males +, +1 female +, +Goasawa +, +Komukawa +, +Asahi-machi +, +Nirasakishi +, + +18.viii.1996 + +, +T + +. + +Hattori +( +SPMN +) + +; + +9 males +, +Hondani +, +Ichinose +, +Enzan-shi +, + +6.vii.1991 + +, +T + +. + +Nozaki +(NKa) + +. + + +Nagano + +: +1 male +, +2 females +, +Oguro-gawa +, +Ina +, +Ina-shi +, + +17.vi.1996 + +, +T + +. + +Hattori +( +SPMN +) + +; + +2 females +, +Sonohara-gawa +, +Achi-mura +, + +20.vi.1994 + +, +T + +. + +Hattori +( +SPMN +) + +. + + +Gifu + +: +1 male +, +Kurumishima +, +Asahi-cho +, +Takayama-shi +, + +16.vii.2012 + +, +H. Iketake +( +HI +) + +. + + +Shizuoka + +: +9 males +, +2 females +, +Hikage-sawa +, +Umegashima +, +Shizuoka-shi +, + +21.vi.2002 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1 female +, +Nishi-hikagezawa +, +Umegashima +, +Shizuoka-shi +, + +16.vii.1995 + +, +T + +. + +Hattori +( +SPMN +) + +; + +6 males +, +1 female +, +Minami-sawa +, +Umegashima +, +Shizuoka-shi +, + +28.vi.1997 + +, +T + +. + +Hattori +( +SPMN +) + +; + +15 males +, +1 female +, same locality, + +4.v.1999 + +, +T + +. + +Hattori +( +SPMN +) + +; + +2 males +, same localiy, + +8.ix.2001 + +, +T + +. + +Hattori +( +SPMN +) + +; + +2 males +, +Ikawa-tôge +, +Umegashima +, +Shizuoka-shi +, + +29.iv.1998 + +, +T + +. + +Hattori +( +SPMN +) + +; + +3 males +, same locality, + +26.vi.2001 + +, +T + +. + +Hattori +( +SPMN +) + +; + +3 males +, +2 females +, +Nigorikawa +, +Umegashima +, +Shizuoka-shi +, + +9.vi.2002 + +, +T + +. + +Hattori +( +SPMN +) + +; + +3 males +, +Yokosawa +, +Shizuoka-shi +, + +4.vi.2001 + +, +T + +. + +Hattori +( +SPMN +) + +; + +1 female +, same data (in glycerin) ( +SPMN +) + +; + +1 female +, same locality, + +9.vi.2001 + +, +T + +. + +Hattori +(in glycerin) ( +SPMN +) + +; + +1 male +, same locality, + +21.v.2003 + +, +T + +. + +Hattori +(in glycerin) ( +SPMN +) + +; + + + + +Etymology. +The Latin species epithet + +“angulicauda + +” (= angle tail) is a noun in apposition referring to the shape of apicodorsal lobe of segment IX in male genitalia of this species. + + + + +Distribution and biology. + +Rhyacophila angulicauda + +sp. nov. +is distributed only in central Honshu, +Japan +( +Fig. 9D +). Adults were collected near mountainous streams from April to August. In some localities, adults of this species and + +R. clemens + +were collected at the same time, but this species tends to be distributed at higher altitudes than + +R. clemens + +in the same river system. + + +Japanese name. +Kakuo-nagare-tobikera. + + + + \ No newline at end of file diff --git a/data/38/55/87/385587AAF73F1169FF4CC15AFD1BA7B4.xml b/data/38/55/87/385587AAF73F1169FF4CC15AFD1BA7B4.xml new file mode 100644 index 00000000000..d285ba81927 --- /dev/null +++ b/data/38/55/87/385587AAF73F1169FF4CC15AFD1BA7B4.xml @@ -0,0 +1,964 @@ + + + +Redescription of Rhyacophila clemens Tsuda 1940 (Trichoptera, Rhyacophilidae), with descriptions of five new, allied species from Japan + + + +Author + +Kawase, Naoki + +text + + +Zootaxa + + +2024 + +2024-05-03 + + +5447 + + +1 + + +55 +76 + + + + +http://dx.doi.org/10.11646/zootaxa.5447.1.3 + +journal article +10.11646/zootaxa.5447.1.3 +1175-5326 +11119209 +3A9842EC-F3D2-4839-9731-AA79A27B25CB + + + + + + + +Rhyacophila inazui + +sp. nov. + + + + + + +( +Figs 4A–4N +, +9C +) + + + + + +Rhyacophila +sp. 2 + +( + +clemens + +gr.): +Inazu 2008 +, 65, 88, 99, wing markings, flight period; +Inazu & Nishida 2011 +, 176, male. + +Rhyacophila +sp. 1 + +( + +clemens + +gr.): +Kawase & Morita 2010 +, 36, list. + + + +Rhyacophila +sp. + +( + +Clemens + +gr.): +Kawase & Morita 2014 +, 4, list. + + + + + +Rhyacophila +sp. E + +: +Nojima 2017 +, 111, list. + + + +Rhyacophila +sp. + +13: + +Yamamoto +et al +. 2021 + +, 70, list. + + + + +Diagnosis. +Adults of this species are unique in the + +R. clemens + +Species Group in having distinct pale yellowish spots along the posterior margin of each forewing ( +Figs 4A, 4B +). The male genitalia of + +R. inazui + +sp. nov. +are very similar to those of + +R. angulicauda + +sp. nov. +and + +R. parvicauda + +sp. nov. +in having a U-shaped apical hinged process of segment X in ventral view, but can be distinguished from the latter two by the size of the apicodorsal lobe of segment IX: The apicodorsal lobe of segment IX is indistinct in the present species ( +Figs 4C, 4E +), but is large and trapezoidal in + +R. angulicauda + +sp. nov. +(arrows indicated in +Figs 5A, 5C +) and small trapezoidal in + +R. parvicauda + +sp. nov. +( +Figs 6A, 6C +). The female genitalia of + +R. inazui + +sp. nov. +are somewhat similar to those of + +R. angulicauda + +sp. nov. +, + +R. parvicauda + +sp. nov. +, and + +R. furcicauda + +sp. nov. +in having almost straight dorsal margins of segment VIII in lateral view, but can be distinguished from the latter three species by the combination of the following two characteristics: (1) the setae on the lateral surface of segment VIII are hair like ( +Figs 4K +, +5F +) in + +R. inazui + +and + +R. angulicauda + +, but thick, spine-like in + +R. parvicauda + +and + +R. furcicauda + +( +Figs 6E +, +7G +); and (2) a pair of ventral ridges extend posterolaterad and can be seen clearly in lateral view in + +R. inazui + +and + +R. parvicauda + +( +Figs 4K +, +6E +) but extend posteroventrad and are invisible in lateral view in + +R. angulicauda + +and + +R. furcicauda + +( +Figs 5F +, +7G +). + + + + +FIGURE 4. + +Rhyacophila inazui + +sp. nov. + +4A, male habitus, left dorsolateral (photographed by K. Inazu); 4B, female right forewing (in alcohol), dorsal; 4C–4H, male genitalia: 4C, left lateral; 4D, segment X and phallic apparatus, left lateral; 4E, dorsal (left inferior appendage omitted); 4F, ventral (left inferior appendage and apical segment of right inferior appendage omitted); 4G1, apical hinged process of segment X, enlarged, ventral; 4G2, ventral plate of aedeagus, enlarged, ventral; 4H, posterodorsal. 4I–4N, female genitalia: 4I, left lateral; 4J, ventral; 4K, segment VIII, left lateral; 4L, same, ventral; 4M, vaginal apparatus, left lateral; 4N, same, ventral. Abbreviation: vr = ventral ridge. Arrows see text. + + + +Adult +( +Figs 4A, 4B +). Length of each forewing: male +6.8–7.8 mm +(mean = 7.3, SD = 0.30, n = 17), female +7.8–9.3 mm +(mean = 8.2, SD = 0.47, n = 8). General morphology and coloration similar to those of + +R. clemens + +, but forewings bearing pale yellowish speckles more densely from base to apical margins ( +Fig. 4A +), distinct pale spots visible even in alcohol ( +Fig. 4B +). In venation, root of fork I on each forewing clearly longer than that of fork II ( +Fig. 4B +). + + +Male genitalia +( +Figs 4C–4H +). Segment IX rectangular in dorsal view with apicodorsal lobe very short ( +Fig. 4E +), dorsal half longer than ventral half in lateral view ( +Fig. 4C +). Preanal appendages absent. Segment X reverse L-shaped in lateral view composed of vertical part and horizontal part: vertical part tall in lateral view ( +Fig. 4D +); horizontal part nearly oval in dorsal view with shallow incisions anteriorly and posteriorly in dorsal view ( +Fig. 4E +); apical hinged process U-shaped in ventral view, with pair of slender finger-like lobes, directed posterodorsad ( +Figs 4C–4F, 4G +1 +), with pair of round anteroventral corners, bearing small median protrusion anteroventrally (arrows in +Figs 4F, 4G +1 +). Anal sclerites composed of two pairs of lobes, each long rectangular in lateral view ( +Fig. 4D +), but apex of dorsal lobe weakly incised mesally in lateral view, bearing common internal root ( +Fig. 4D +). Apical band well developed, semi-oval in lateral view, broadly surrounding anus and base of anal sclerites ( +Figs 4D, 4F, 4H +). Tergal band connecting base of apical band to dorsum of phallobase ( +Fig. 4D +). Basal segment of each inferior appendage setose, elongate, posterior half gradually thicker in lateral view ( +Fig. 4C +). Apical segment of each inferior appendage rounded triangular in lateral view ( +Fig. 4C +), covered with hair-like setae mesally ( +Fig. 4E +). In phallic apparatus, phallobase short ( +Fig. 4D +); aedeagus forming narrow tube with sclerotized ventral plate ( +Figs 4D, 4F, 4H +); ventral plate horizontal and tongue-shaped with posterior margin shallowly concave in ventral view ( +Fig. 4G +2 +). Parameres absent. + + +Female genitalia +( +Figs 4I–4N +). Segment VIII annular, dorsal margin almost straight in lateral view ( +Figs 4I, 4K +), slightly flattened ventrally; with pair of distinct ventral ridges extending posterolaterad in lateral view, gradually separating from anterior to posterior in lateral and ventral views ( +Figs 4I–4L +); pair of apodemal rods reaching posterior end of segment VI ( +Fig. 4I +). Segment IX membranous, with pair of apodemal rods dorsolaterally extending into abdominal segment VII ( +Fig. 4I +). Vaginal apparatus simple; posterior process sclerotized, smooth, rectangular, about three times as long as wide in lateral view ( +Fig. 4M +), oval in ventral view ( +Fig. 4N +); processus spermathecae membranous ( +Figs 4M, 4N +). + + +Immature stage +. Unknown. + + + + + + +Holotype +. + +Male +(in alcohol), +Amago-ike +, +Takenouchi +, +Wadayama-cho +, +Asago-shi +, +Hyogo Pref. +, +Honshu +, +Japan +, +35°24’21”N +134°55’13”E +, alt. + +250 m + +, + +16.iv.2004 + +, +K. Inazu +( +LBM1410012601 +). + + + + + +Paratypes +. +Honshu +: +Ishikawa + +: +1 male +, +Sannomiya +, +Tsurugi-machi +, +Hakusan-shi +, + +20.iv.1986 + +, +I. Togashi +( +OMNH +). + +Shizuoka + +: +2 males +, +Warashina-gawa +, +Ôma +, +Shizuoka-shi +, + +3.iv.1994 + +, +T + +. + +Hattori +(SPMN-IS-59752–59753); +1 male +, +Utaugenotaki +, +Kurata +, +Fujieda-shi +, + +24.iii.2004 + +, +T + +. + +Hattori +(SPMN-IS-59754). + +Shiga + +: +16 males +, +Sugino +, +Kinomoto-cho +, +Nagahama-shi +, + +12.iv.2012 + +, +T + +. + +Hattori +( +LBM1410012602–1410012617 +). + +Kyoto + +: +1 male +, +Kibune +, +Kyoto-shi +, + +11.iv.1990 + +, +K. Tanida +( +OMNH +). + +Osaka + +: +1 male +& +1 female +(couple), same locality, + +10.iv.1990 + +, +K. Tanida +( +OMNH +) + +; + +1 male +& +1 female +(couple), +Ishi-kawa +, +Takihata-horikoshi +, Kawachi-nagano-shi, + +20.iv.1987 + +, +K. Tanida +( +OMNH +). + +Hyogo + + +: + +1 male +, +2 females +, same data as the holotype ( +LBM1410012618–1410012620 +). + +Okayama + +: +5 males +, +4 females +, +Shiraka-keikoku +, +Tomi-nishidani +, +Kaganino-cho +, + +23.iv.2017 + +, +K. Nojima +( +LBM1410012621– 1410012629 +) + +; + + +Other specimens examined. Honshu: + + +Shizuoka + +: +1 male +, +Nakazawa +, +Shizuoka-shi +, + +21.iii.1995 + +, +T +. +Hattori +( +SPMN +) + +; + + +Gifu + +: +1 female +, +Sakauchi-sakamoto +, +Ibigawa-cho +, + +10–20.iv.2023 + +, +N. Kawase +(NKa) + +. + + +Mie + +: +10 males +, +5 females +, +Kanzan +, +Suizawa-cho +, +Yokkaichi-shi +, + +6–16.iv.2008 + +, +H. Morita +(NKa) + +; + +3 males +, +Miyazuma-kyo +, +Suizawa-cho +, +Yokkaichi-shi +, + +6.iv–16.iv.2009 + +, H. +Morita +( +SPMN +) + +. + + +Shiga + +: +16 males +, +2 females +, +Nakanokawachi +, +Yogo-cho +, +Nagahama-shi +, + +26.iv–17.v.2010 + +, +N. Kawase +(NKa) + +; + +1 male +, +Ôkawara +, +Tsuchiyama-cho +, +Kôka-shi +, + +21.iv.2005 + +, +N. Kawase +(NKa) + +. + + +Hyogo + +: +1 male +, +1 female +, +Itoi-gawa +, +Wadayama-cho +, +Asago-shi +, + +5.iv.2002 + +, K. +Inazu +(in glycerin) ( +SPMN +) + +; + +2 males +, +2 females +, same locality, + +6.iv.2004 + +, K. +Inazu +( +SPMN +) + +; + +5 males +, +Wakasu +, +Sayô-cho +, + +25.iv.1984 + +, H. +Nishimoto +( +SPMN +) + +. + + +Osaka + +: +2 males +, +Takihata +, Kawachi-nagano-shi, + +25.iv.1985 + +, H. +Nishimoto +( +SPMN +) + +. + + +Nara + +: +1 male +, +Gojyô-shi +, + +12.iv.1984 + +, H. +Nishimoto +( +SPMN +) + +. + + +Tottori + +: +3 males +, +Wakasa-cho +, + +24.iv.1984 + +, H. +Nishimoto +(in glycerin) ( +SPMN +) + +; + +3 males +, same data (in glycerin) ( +SPMN +) + +. + + +Okayama + +: +1 male +, +Ombara +, +Kamisaibara +, +Kagamino-cho +, + +13.iv.2019 + +, +K. Nojima +(NKa) + +; + +4 males +, +Ôgaya +, Nishi-awakura-son, + +7.v.2017 + +, +K. Nojima +(NKa). + +Shikoku + + +: + + +Ehime + +: +1 female +, +Izugataniyama +, +Nishidani +, +Kumakôgen-cho +, + +1–10.v.2018 + +, +E. Yamamoto +(NKa) + +; + +2 males +, +Namakusa-dani +, +Odamiyama +, +Uchiko-cho +, + +21.iv.2000 + +, E. +Yamamoto +, +T +. +Ito +& +A. Ohkawa +( +SPMN +) + +; + +10 males +, +1 female +, same locality, + +29.iv.2000 + +, E. +Yamamoto +( +SPMN +) + +; + +1 male +, +3 females +, same locality, + +21–30.iv.2020 + +, +E. Yamamoto +(NKa) + +. + + +Kochi + +: +1 male +, +Befu-kyo +, +Monobe-son +, + +12.iv.2004 + +, K. +Nio +( +SPMN +) + +. + + + + +Distribution and biology. + +Rhyacophila inazui + +sp. nov. +is distributed in central to western Honshu and Shikoku ( +Fig. 9C +). The adults were collected near mountain streams in spring, late March to early May. + + + + +Etymology. +This species is dedicated to Mr. Kazuyuki Inazu, who mentioned this species as a possibly undescribed species based on its early flight season and wing color pattern ( +Inazu, 2008 +). The species epithet is a noun in the genitive case. + + +Japanese name +. Inazu-nagare-tobikera. + + + + \ No newline at end of file diff --git a/data/38/55/B3/3855B31D2432FFDA1C1CA7C7F2F89200.xml b/data/38/55/B3/3855B31D2432FFDA1C1CA7C7F2F89200.xml new file mode 100644 index 00000000000..e97d88fd64f --- /dev/null +++ b/data/38/55/B3/3855B31D2432FFDA1C1CA7C7F2F89200.xml @@ -0,0 +1,157 @@ + + + +Order Soricomorpha + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +220 +311 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Sorex (Otisorex) bairdi +Merriam 1895 + + + + + + + +Sorex (Otisorex) bairdi +Merriam 1895 + +, +N. Amer. Fauna, 10: 77 + +. + + + + +Type Locality: + +USA +, +Oregon +, [Clatsop Co.], Astoria. + + + + + +Vernacular Names: +Baird's Shrew +. + + + + +Subspecies: +: + + +Subspecies + +Sorex (Otisorex) bairdi +subsp. +bairdi +Merriam 1895 + + + +Subspecies + +Sorex (Otisorex) bairdi +subsp. +permiliensis +Jackson 1918 + + + + + +Distribution: +NW +Oregon +( +USA +). + + + + +Conservation: +IUCN +– Lower Risk (lc). + + + + +Discussion: +Subgenus + +Otisorex + +; + +S. vagrans + +complex ( +Carraway, 1990 +; +Demboski and Cook, 2001 +). This taxon has been alternatively referred to +obscurus +, + +vagrans + +, and +monticulus +, but was given specific rank by +Carraway (1990) +. Includes +permiliensis +as a valid subspecies ( +Alexander, 1996 +; +Carraway, 1990 +). + + + + \ No newline at end of file diff --git a/data/38/56/3F/38563F608A537612F3265B57625B45A4.xml b/data/38/56/3F/38563F608A537612F3265B57625B45A4.xml new file mode 100644 index 00000000000..62bd7bc247a --- /dev/null +++ b/data/38/56/3F/38563F608A537612F3265B57625B45A4.xml @@ -0,0 +1,130 @@ + + + +Aquatic Insects from the Caatinga: checklists and diversity assessments of Ubajara (Ceara State) and Sete Cidades (Piaui State) National Parks, Northeastern Brazil + + + +Author + +Takiya, Daniela Maeda + + + +Author + +Santos, Allan Paulo Moreira + + + +Author + +Pinto, Angelo Parise + + + +Author + +Henriques-Oliveira, Ana Lucia + + + +Author + +Carvalho, Alcimar do Lago + + + +Author + +Sampaio, Brunno Henrique Lanzellotti + + + +Author + +Clarkson, Bruno + + + +Author + +Moreira, Felipe Ferraz Figueiredo + + + +Author + +Avelino-Capistrano, Fernanda + + + +Author + +Goncalves, Ines Correa + + + +Author + +Cordeiro, Isabelle da Rocha Silva + + + +Author + +Camara, Josenir Teixeira + + + +Author + +Barbosa, Julianna Freires + + + +Author + +de Souza, W. Rafael Maciel + + + +Author + +Rafael, Jose Albertino + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8354 +8354 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8354 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8354 +1314-2828--8354 + + + + +Metachela Coquillett, 1903 + + + +Notes +New genus record for CE. + + + \ No newline at end of file diff --git a/data/38/56/42/385642FC49D9EDCB2358504D2AD7F077.xml b/data/38/56/42/385642FC49D9EDCB2358504D2AD7F077.xml new file mode 100644 index 00000000000..7cfa8ae415c --- /dev/null +++ b/data/38/56/42/385642FC49D9EDCB2358504D2AD7F077.xml @@ -0,0 +1,618 @@ + + + +Flora of Cameroon - Annonaceae Vol 45 + + + +Author + +Couvreur, Thomas L. P. +https://orcid.org/0000-0002-8509-6587 +IRD, DIADE, Univ Montpellier, Montpellier, France & Universite de Yaounde I, Ecole Normale Superieure, Departement des Sciences Biologiques, Laboratoire de Botanique systematique et d'Ecologie, B. P. 047, Yaounde, Cameroon & Naturalis Biodiversity Center, Botany Section, Darwinweg 2, 2333 CR Leiden, Netherlands +thomas.couvreur@ird.fr + + + +Author + +Dagallier, Leo-Paul M. J. +https://orcid.org/0000-0002-3270-1544 +IRD, DIADE, Univ Montpellier, Montpellier, France + + + +Author + +Crozier, Francoise +IRD, DIADE, Univ Montpellier, Montpellier, France + + + +Author + +Ghogue, Jean-Paul +Universite de Yaounde I, Ecole Normale Superieure, Departement des Sciences Biologiques, Laboratoire de Botanique systematique et d'Ecologie, B. P. 047, Yaounde, Cameroon & Green Connexion, Environmental Group, siege face GP Melen, a cote de l'immeuble Palais des verres. Yaounde, Cameroun + + + +Author + +Hoekstra, Paul H. +Naturalis Biodiversity Center, Botany Section, Darwinweg 2, 2333 CR Leiden, Netherlands + + + +Author + +Kamdem, Narcisse G. +Universite de Yaounde I, Ecole Normale Superieure, Departement des Sciences Biologiques, Laboratoire de Botanique systematique et d'Ecologie, B. P. 047, Yaounde, Cameroon + + + +Author + +Johnson, David M. +https://orcid.org/0000-0003-2896-7419 +Department of Botany-Microbiology, Ohio Wesleyan University, Delaware, OH, 43015, USA + + + +Author + +Murray, Nancy A. +Department of Botany-Microbiology, Ohio Wesleyan University, Delaware, OH, 43015, USA + + + +Author + +Sonke, Bonaventure +https://orcid.org/0000-0002-4310-3603 +Universite de Yaounde I, Ecole Normale Superieure, Departement des Sciences Biologiques, Laboratoire de Botanique systematique et d'Ecologie, B. P. 047, Yaounde, Cameroon + +text + + +PhytoKeys + + +2022 + +2022-09-20 + + +207 + + +1 +532 + + + + +http://dx.doi.org/10.3897/phytokeys.207.61432 + +journal article +http://dx.doi.org/10.3897/phytokeys.207.61432 +1314-2003-207-1 +29CD4EF8FB525DBAA022DF25CDB649C9 + + + + + +Artabotrys rufus De Wild., Bull. Jard. Bot. +Etat +Bruxelles 4: 386, 1914 + + + + + +Figs 16 +, 17 +; Map 2H + + + + += Artabotrys boonei +De Wild., Repert. Spec. Nov. Regni Veg. 13: 383, 1914. Syn. nov. Type. Democratic Republic of the Congo. Orientale, Nala, Boone A. 80, 1911: lectotype, sheet here designated: BR[BR0000008820365]; isotype: BR[BR0000008820372]. + + += Artabotrys dahomensis +Engl. & Diels, Notizbl. +Koenigl +. Bot. Gart. Berlin 2: 299, 1899. Syn. nov. Type. Benin: Dahome, +Newton s.n. +, 1886: holotype: B[B 10 0153018]. + + += Artabotrys setulosus +Mildbr. & Diels, Bot. Jahrb. Syst. 53. 447, 1915. Type. Cameroon. East Region, Mulundou, +Mildbraed G.W.J. 4999 +, 26 Jan 1911: lectotype, here designated: HBG[HBG502545]. + + + + +Type +. + + + +Democratic Republic of the Congo +. Equateur; Likimi, + +Malchair L. +274 + +, +20 Avr 1910 +: +holotype +: BR[BR0000008820297] + + + + +Description. + +Liana, to 20 m tall, d.b.h. 3-5 cm. Indumentum of simple hairs; old leafless branches sparsely pubescent, +young foliate branches hirsute, with erect hairs. +Leaves: petiole 2-4 mm long, 1-2 mm in diameter, +hirsute +, slightly grooved, blade inserted on top of the petiole; +blade 8-14 cm long +, 3.5-5.5 cm wide, oblong to obovate, apex acuminate, acumen 0.5-1 cm long, base rounded to subcordate or obtuse, papyraceous, below pubescent when young and old with long appressed hairs, above glabrous when young and old, concolorous; midrib impressed, above glabrous when young and old, below pubescent when young and old; secondary veins 9 to 12 pairs, glabrous above; tertiary venation reticulate. Individuals bisexual; inflorescences ramiflorous on old leafless branches, leaf opposed. Flowers with 9 perianth parts in 3 whorls, 1 to 3 per inflorescence, hook-shaped peduncle 4-7 mm long; pedicel 3-5 mm long, ca. 1 mm in diameter, +pubescent to sparsely hirsute +; in fruit 3-15 mm long, ca. 2 mm in diameter, pubescent; bracts caduceus, not seen; sepals 3, valvate, free, 5-7 mm long, 2-4 mm wide, triangular, apex acute, base truncate, green, +hirsute outside, glabrous inside +, margins flat; petals free, sub equal, green turning yellow; outer petals 3, 10-20 mm long, 3-4 mm wide, very narrowly elliptic to linear, apex acute, base rounded to broad and concave, green turning bright yellow, + +margins flat, recurved inwards +in vivo + +, densely appressed-pubescent outside, appressed-pubescent to glabrous inside; inner petals 3, valvate, 12-20 mm long, 2-3 mm wide, very narrowly elliptic to linear, apex acuminate to acute, base broad and concave, green turning bright yellow, margins flat, recurved inwards +in vivo +, appressed-pubescent outside, appressed-pubescent inside; stamens 60 to 70, in ca. 5 rows, ca. 1 mm long, broad; connective discoid, glabrous, green; staminodes absent; carpels free, 8 to 10, ovary ca. 1 mm long, stigma capitate, glabrous. Monocarps sessile, 5 to 11, 12-15 mm long, 5-6 mm in diameter, ellipsoid to fusiform, +apex apiculate, glabrous, smooth +, not ribbed, red when ripe; seeds 1 to 2 per monocarp, 10-12 mm long, 5 mm in diameter, ellipsoid to oblong; aril absent. + + + +Figure 16. + +Artabotrys rufus + +A +leaf, upper side +B +base of leaf blade, upper side +C +base of leaf bade, lower side +D +branch, note erect hairs +E +flowering branch +F +flower, side view +G +detail of receptacle, 4 petals removed +H +flower, top view +A-H +Couvreur 854 +, Gabon. Photos Thomas L.P. Couvreur. + + + + +Distribution. +A mainly central African species, from Benin to Nigeria and Cameroon to the Republic of the Congo and in the Democratic Republic of the Congo; in Cameroon known from the Central and East regions. + + +Habitat. +A fairly common species, in secondary lowland or premontane rain forests. Altitude 400-900 m a.s.l. + + +Local and common names known in Cameroon. + +nginda ( +pygmee-bibaya +) ( +Letouzey 1964 +). + + + +IUCN conservation status. +Not evaluated. + + +Uses in Cameroon. +None recorded. + + +Notes. + + +Artabotrys rufus + +is distinguished by the hirsute pubescence of the young foliate branches, petioles, peduncles and flowering pedicels, its leaves that are elliptic, apiculate and less than 14 cm long, with long (1-2 mm) appressed hairs on the lower side of the leaf blade and a rounded to subcordate or obtuse base, a short peduncle (generally less than 7 mm long), petals with long dense brown hairs and smooth apiculate monocarps. The tertiary venation is also clearly visible forming clear loops towards the margins of the leaves. + + + +Artabotrys rufus + +resembles + +A. velutinus + +being pubescent, but the pubescence of + +A. velutinus + +is not hirsute, with shorter hairs and more tomentose on the young foliate branches and petioles. The petals are also very similar being curved inwards, giving them the appearance of a tube. It is possible that both names are synonymous. + +Artabotrys rufus + +is also very close morphologically to the west African species + +A. hispidus + +Sprague & Hutch. by its hirsute pubescence and the shape of the leaves and flowers. It is also very possible that these names are synonymous. Several specimens from Cameroon where identified as + +A. hispidus + +, but upon closer look we have identified them as belonging to + +A. rufus + +. Several authors ( +Boutique 1951b +; +Le Thomas 1969b +) have suggested that the name + +A. rufus + +might be synonym with the east African + +A. rupestris + +Diels, although Verdcourt +didn't +recognize this synonymy ( +Verdcourt 1971a +) suggesting differences in the leaves. + + +We here synonymize the names + +A. boonei + +and + +A. dahomensis + +with + +A. rufus. + +The former name was considered a synonym of + +A. velutinus + +( +Lebrun and Stork 1991 +), but the type clearly suggests it is a synonym of + +A. rufus + +(if the latter is really distinct from + +A. velutinus + +). + + + +Figure 17. + +Artabotrys thomsonii + +A +flowering branch +B +outer petal, inner view +C +inner petal, inner view +D +flowering receptacle, petals removed +E +stamens, front and side views +F +carpel, side and detail of ovules +G +fruiting peduncle. + +Artabotrys rufus + +H +flowering branch +I +flowering receptacle with one outer petal removed +J +outer petals, outer view and inner views +K +inner petals, inner and outer views +L +flowering receptacle, petals removed +M +stamen +N +carpel, side view and detail of ovule +O +fruiting peduncle +A-G +from +Le Testu 9249 +H-N +from +Hall 3193 +; 15 from +Hall 3528 +. Drawings by +Helene +Lamourdedieu, Publications Scientifiques du +Museum +national +d'Histoire +naturelle, Paris; modified from +Le Thomas (1969b +, pl. 23, p. 441 ( + +A. rufus + +)). + + + +More detailed studies across the range of these species ( + +A. hispidus + +, + +A. rufus + +, + +A. rupestris + +and + +A. velutinus + +) are needed to determine if there is one single widespread species from west to east Africa (possibly with different infraspecific taxa), or if there are several different species possibly grouped into a species complex ( +Hawthorne and Jongkind 2006 +). + + + +Specimens examined. + +Central Region +: + +Febe +Mount, +3.91°N +, +11.48°E +, + +30 March 1962 + +, + +Breteler F.J. + +2717 (A,BR,K,P,WAG,YA); Mont Mbam Minkon on trail +5 km +from +Nkol Nyada village +On top of small hill, +3.97°N +, +11.40°E +, + +21 March 2013 + +, + +Couvreur T.L.P. + +418 (MPU,WAG,YA); Nachtigal, +4.35°N +, +11.63°E +, + +01 July 1964 + +, + +de Wilde W.J.J.O + +2779 (P,WAG,YA); Nkolbison, +3.88°N +, +11.45°E +, + +02 November 1964 + +, + +de Wilde W.J.J.O + +3715 (BR,K,P,WAG); Left bank +Sanaga river +near Ferry Nachtigal ca + +20 km +N of Obala + +, +4.34°N +, +11.64°E +, + +29 April 1965 + +, + +Leeuwenberg A.J.M. + +6011 (B,BR,C,K, MO,P,WAG,YA). + +East Region + +: Dimako, +4.38°N +, +13.57°E +, + +02 August 1961 + +, + +Breteler F.J. + +1752 (P,YA); Bertoua +15 km +along road to Deng Deng, +4.66°N +, +13.63°E +, + +31 August 1961 + +, + +Breteler F.J. + +1825 (WAG); +Bamekok +(Batouri), +4.2°N +, +14.15°E +, + +16 April 1962 + +, + +Breteler F.J. + +2825 (P,WAG); +60 km +south of +Yokadouma +5 km +south of + +Masea +village + +, +3.10°N +, +14.84°E +, + +06 March 2019 + +, + +Couvreur T.L.P. + +1211 (MPU,WAG,YA); A +25 km +au + +NE de +Bange + +km 75 route Yokadouma-Moloundou, +3.02°N +, +15.12°E +, + +25 May 1963 + +, + +Letouzey R. + +5147 (P,YA); Mbatika-Malen +20 km +de Moloundou +route Yokadouma +2.03°N +, +15.22°E +, + +22 April 1971 + +, + +Mezili P. + +193 (P,YA); Moloundou near Lokomo Bumba and +Bange +, +2.08°N +, +15.25°E +, + +26 January 1911 + +, + +Mildbraed G.W.J. + +4350 (B,HBG); +Foret +inhabitee +entre Yokaduma et Assobam +, +3.52°N +, +15.05°E +, + +24 April 1911 + +, + +Mildbraed G.W.J. + +4999 (B,HBG) + +. + + + + \ No newline at end of file diff --git a/data/38/56/4D/38564DD8844458AB87770294FD414BC4.xml b/data/38/56/4D/38564DD8844458AB87770294FD414BC4.xml new file mode 100644 index 00000000000..a9e2f3d35b4 --- /dev/null +++ b/data/38/56/4D/38564DD8844458AB87770294FD414BC4.xml @@ -0,0 +1,126 @@ + + + +Lizards (Reptilia: Squamata) from the Caatinga, northeastern Brazil: Detailed and updated overview + + + +Author + +Uchoa, Lucas Rafael +Centro de Estudos Superiores de Caxias, Universidade Estadual do Maranhao, Programa de Pos-Graduacao em Biodiversidade, Ambiente e Saude, Praca Duque de Caxias, 65604 - 380, Caxias, MA, Brazil + + + +Author + +Delfim, Fagner Ribeiro +Departamento de Sistematica e Ecologia, Centro de Ciencias Exatas e da Natureza, Universidade Federal da Paraiba, 58059 - 800, Joao Pessoa, PB, Brazil + + + +Author + +Mesquita, Daniel Oliveira +Departamento de Sistematica e Ecologia, Centro de Ciencias Exatas e da Natureza, Universidade Federal da Paraiba, 58059 - 800, Joao Pessoa, PB, Brazil + + + +Author + +Colli, Guarino Rinaldi +Departamento de Zoologia, Universidade de Brasilia, 70910 - 900, Brasilia, DF, Brazil + + + +Author + +Garda, Adrian Antonio +Departamento de Botanica e Zoologia, Universidade Federal do Rio Grande do Norte, 59078 - 900, Natal, RN, Brazil + + + +Author + +Guedes, Thais B. +https://orcid.org/0000-0003-3318-7193 +Departamento de Biologia Animal, Instituto de Biologia, Universidade Estadual de Campinas, 13083 - 862, Campinas, SP, Brazil & University of Gothenburg, Gothenburg Global Biodiversity Center, Department of Biological and Environmental Sciences, Box 461, SE- 405 30, Goeteborg, Sweden +thaisbguedes@yahoo.com.br + +text + + +Vertebrate Zoology + + +2022 + +2022-08-12 + + +72 + + +599 +659 + + + + +http://dx.doi.org/10.3897/vz.72.e78828 + +journal article +http://dx.doi.org/10.3897/vz.72.e78828 +2625-8498-72-599 +A1E3C31522684C20AA3C6771D37D4A74 +162E581A572D558DA12337F50136919B + + + + +Eurolophosaurus sp. + + + + +Fig. 19 + + + +Distribution. + +Caatinga endemic species. It is recorded only in the state of Bahia. It shows restricted distribution in the Caatinga and with annual mean temperature 20 to 28°C along two ecoregions (Table +1 +; Appendix S3). Distributed in high elevation areas (634-1,391 m a.s.l.), with annual mean temperature 19 to 23°C, and average annual rainfall between 638 and 1,019 mm. + + + +Ecological notes. + +Terrestrial and diurnal. It is a species of + +Eurolophosaurus + +related to + +Eurolophosaurus nanuzae + +( +Rodrigues et al. 2006 +). Occurring in areas of white sandy soils covered by an open cerrado like vegetation, mixed with that of campos rupestres ( +Rodrigues et al. 2006 +). Diet based mainly on arthropods, no information about the preferred items on the diet of this species is known. Oviparous, no detailed data is known about the number of eggs laid by the species, but it could be similar to other + +Eurolophosaurus + +( +Galdino et al. 2003 +; +Rocha and Rodrigues 2005 +; +Xavier et al. 2021 +). + + + + \ No newline at end of file diff --git a/data/38/56/53/385653AEF459A78871EA3413711E4F11.xml b/data/38/56/53/385653AEF459A78871EA3413711E4F11.xml new file mode 100644 index 00000000000..77cbd1391bb --- /dev/null +++ b/data/38/56/53/385653AEF459A78871EA3413711E4F11.xml @@ -0,0 +1,73 @@ + + + +Checklist of British and Irish Hymenoptera - Braconidae + + + +Author + +Broad, Gavin R. + + + +Author + +Shaw, Mark R. + + + +Author + +Godfray, H. Charles J. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8151 +8151 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8151 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8151 +1314-2828-4-8151 + + + + +Cyanopterus Haliday, 1835 + + + +Notes + +species excluded from the British and Irish list by +Shaw and Quicke (1999) +: + + +[flavator (Fabricius, 1793, +Ichneumon +); syn. flavulator (Ratzeburg, 1844, +Bracon +); longipalpis (Thomson, 1892, +Bracon +); barcinonensis (Marshall, 1897, +Coeloides +)] + + + + \ No newline at end of file diff --git a/data/38/56/58/38565874209F70A580EE3EAF55F5EAFB.xml b/data/38/56/58/38565874209F70A580EE3EAF55F5EAFB.xml new file mode 100644 index 00000000000..01bc167a648 --- /dev/null +++ b/data/38/56/58/38565874209F70A580EE3EAF55F5EAFB.xml @@ -0,0 +1,74 @@ + + + +Polychaetes of Greece: an updated and annotated checklist + + + +Author + +Faulwetter, Sarah + + + +Author + +Simboura, Nomiki + + + +Author + +Katsiaras, Nikolaos + + + +Author + +Chatzigeorgiou, Giorgos + + + +Author + +Arvanitidis, Christos + +text + + +Biodiversity Data Journal + + +2017 + +5 + + +20997 +20997 + + + + +http://dx.doi.org/10.3897/BDJ.5.e20997 + +journal article +http://dx.doi.org/10.3897/BDJ.5.e20997 +1314-2828--20997 + + + + +Branchiomma bombyx (Dalyell, 1853) + + + + +Branchiomma bombyx +(Dalyell, 1853) | +Dasychone bombyx +(Dalyell, 1853) + + + + \ No newline at end of file diff --git a/data/38/56/ED/3856EDFA45B03A34248C99A0BDB1A32C.xml b/data/38/56/ED/3856EDFA45B03A34248C99A0BDB1A32C.xml new file mode 100644 index 00000000000..336220e11f1 --- /dev/null +++ b/data/38/56/ED/3856EDFA45B03A34248C99A0BDB1A32C.xml @@ -0,0 +1,89 @@ + + + +Order Primates + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +111 +184 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Colobus satanas +subsp. +satanas +Waterhouse 1837 + + + + + + + +Colobus satanas +subsp. +satanas +Waterhouse 1837 + +, +Proc. Zool. Soc. Lond., 1837: 87 + +. + + + + +Type Locality: + +Equatorial Guinea +, Bioko. + + + + + +Synonyms: + +Colobus satanas +subsp. +metternichi +Krumbiegel 1943 + +. + + + + \ No newline at end of file diff --git a/data/38/57/8D/38578D42627584656E396DDF429747D3.xml b/data/38/57/8D/38578D42627584656E396DDF429747D3.xml new file mode 100644 index 00000000000..04ef8641eba --- /dev/null +++ b/data/38/57/8D/38578D42627584656E396DDF429747D3.xml @@ -0,0 +1,153 @@ + + + +Targeting a portion of central European spider diversity for permanent preservation + + + +Author + +Candek, Klemen + + + +Author + +Gregoric, Matjaz + + + +Author + +Kostanjsek, Rok + + + +Author + +Frick, Holger + + + +Author + +Kropf, Christian + + + +Author + +Kuntner, Matjaz + + + +Author + +Miller, Jeremy A. + + + +Author + +Hoeksema, Bert W. + +text + + +Biodiversity Data Journal + + +2013 + +1 + + +980 +980 + + + + +http://dx.doi.org/10.3897/BDJ.1.e980 + +journal article +http://dx.doi.org/10.3897/BDJ.1.e980 +1314-2828-1 + + + + +phalangioides +Pholcus +Pholcidae +Animalia + + + + +Pholcus phalangioides (Fuesslin, 1775) + + + +Materials + + +Type status: +Other material +Occurrence: recordedBy: + +Kuntner, +Candek + +; sex: +1 female +, +1 male +; Location: locationID: SI50; country: +Slovenia +; locality: + +Sp. +Praprece + +; minimumElevationInMeters: 351; maximumElevationInMeters: 351; decimalLatitude: +46.1620 +; decimalLongitude: +14.6933 +; Event: eventDate: +2010-08-03/2012-05-28 +; habitat: house and surroundings + + + + +Type status: +Other material +Occurrence: recordedBy: + +Kostanjsek +, +RTSB +2011 + +; sex: +1 female +; Location: locationID: SI68; country: +Slovenia +; locality: + +Sv. Jurij ob +Scavnici + +; minimumElevationInMeters: 235; maximumElevationInMeters: 235; decimalLatitude: +46.5687 +; decimalLongitude: +16.0223 +; Event: eventDate: +2011-07-22 +; habitat: school + + + + + \ No newline at end of file diff --git a/data/38/57/BD/3857BD64FFA1FFD9FF6C4B4B4A8EFEE6.xml b/data/38/57/BD/3857BD64FFA1FFD9FF6C4B4B4A8EFEE6.xml new file mode 100644 index 00000000000..59b4f3e8df2 --- /dev/null +++ b/data/38/57/BD/3857BD64FFA1FFD9FF6C4B4B4A8EFEE6.xml @@ -0,0 +1,403 @@ + + + +Contribution to the taxonomy and nomenclature of Entiminae from the Palaearctic region and South Africa (Coleoptera: Curculionidae) + + + +Author + +Yunakov, N. N. + + + +Author + +Klass K. D. + +text + + +Beiträge Zur Entomologie = Contributions to Entomology + + +2012 + +2012-12-20 + + +62 + + +2 + + +427 +445 + + + + +https://www.contributions-to-entomology.org/article/view/1825 + +journal article +2560 +10.21248/contrib.entomol.62.2.427-445 +97bcdde4-9fc2-4696-9d82-7a0a5e2be65f +0005-805X +4779554 + + + + + + + + + +Wittmerella +PESARINI +, 1973: 81 + + + + + + + + + +[ +type +species: + +Wittmerella viridisetosa +Pesarini, 1973 + +; by original designation] + + + + + + + +Sciaphilomorphus +Alonso-Zarazaga & Lyal, 1999: 177 + + +, +syn. n. + + + +[ +type +species: + +Sciaphilus aurosus +Boheman, 1845 + +; by original designation] + + + + + +Wittmerella viridisetosa + +is the only species assigned to this genus, and males are unknown. The original description in +Pesarini (1973) +is overall sufficient, but there are some gaps to be filled. + + +Partial redescription: + + +Measurements. +Body length +3.65-4.80 mm +, width +1.55-1.75 mm +. +Female genitalia. +Sternite VIII with very transverse lamella and long, thin apodeme. Caput of apodeme vestigial. Ovipositor with coxite undivided, poorly setose, without styli ( +Fig. 56 +). Spermatheca robust, ramus and collum situated very close to one another, vestigial (can be recognized by junction of spermathecal gland duct and ductus spermaticus, respectively); corpus not swollen. ( +Figs 44-45 +). + + + + +Diagnosis: + + +The structure and shape of the antennae and rostrum in + +Wittmerella + +(including + +Sciaphilomorphus + +) are very similar to those of + +Polydrusus + +subgenus + +Leucodrusus +Stierlin, 1884 + +and + +Sauromates arnoldii +Korotyaev, 1992 + +, which suggests these groups to be related to each other ( +Figs 34, 37 +). + + +Taxonomic notes: + + + +Sciaphilomorphus + +includes two small species (body length +3-4 mm +) occurring in +Italy +, +Tunisia +and +Algeria +: + +S. aurosus +(Boh.) + +and + +S. sulcirostris +(Chevr.) + +. Both are wingless, and the pterothorax is strongly modified as a consequence of this (as convergently in many +Entiminae +). The aedeagus of + +Sciaphilomorphus sulcirostris + +and + +S. aurosus + +has dentate ligulae ( +Fig. 49 +). The internal sac has a densely spiculate field in its apical half, and the aggonoporium is almost unarmed. The tegmen is heavily sclerotized, the tegminal plate with the parameres is well developed ( +Fig. 50 +). The furcal arms of male sternite IX are heavily sclerotized ( +Fig. 51 +). Tergite VIII has a deep apical groove ( +Fig. 52 +). + + +The previous proposal of identity of + +Sciaphilomorphus + +with + +Stasiodis +Gozis, 1886 ( +Yunakov 2006 +) + +seems to be inappropriate, misled by the extreme similarity in general appearance due to body miniaturization. + +Stasiodis + +is distinct from + +Sciaphilomorphus + +by its tenuous antennal scape and slender funicular segments, ligulae of median lobe membranous, aggonoporium with well developed armature, parameres fused in proximal half, male tergite VIII without transverse groove ( +Figs 52-55 +), ramus and collum of spermatheca situated far apart, coxites of ovipositor with well developed styli, and sternite VIII with large lamella ( +Figs 46-47 +, +57 +). + + + +Sciaphilomorphus + +and + +Wittmerella viridisetosa + +( + +Figs +5-8 + +in +Pesarini 1973 +) are also very similar in general appearance, but also in most morphological details. They share a similar structure of the epistomal area: epistome fused with frons, glabrous, bearing well visible pores, with few pairs of chaetae. The morphology of the female postabdomen is also very similar: sternite VIII with large small, transverse lamella; ramus and collum of spermatheca situated very close to one another. + +Wittmerella + +differs from both + +Sciaphilomorphus +species + +by the vestigial condi-condition of the lateral edges of the rostrum posteriad of the antennal articulation ( +Fig. 35 +), by the elongate body shape, and by the pterothorax being less modified along the winglessness syndrome. We consider this insufficient to justify the separation of two genera, + +Wittmerella + +and + +Sciaphilomorphus + +. + + +On this basis we consider + +Sciaphilomorphus + +congeneric with + +Wittmerella + +, and the following new combinations are proposed here: + +Wittmerella aurosa +(Boheman, 1845) + +, +comb. n. +, + +W. sulcirostris +(Chevrolat, 1860) + +, +comb. n. + + + + + +Type +material: + + + + + +W. viridisetosa + +: + +Iran +: + +Holotype +, female ( +NMB +) (L: +4.8 mm +; W: +1.75 mm +) ‘Polour-Abali 17.5. / +2100 +/2600m’, ‘Iran 1970 / Wittmer, v. Bothmer’, ‘ + +Wittmerella viridisetosa + +m. Holotypus’; + + +Paratype +, female ( +NMB +) (L: +4.2 mm +, W: +1.7 mm +): labeled as +holotype + +. + + +Other material examined: + + + +W. viridisetosa + +: + + +Turkey + +: +3 females +( +MTMB 2 +, +ZIN 1 +): ‘ +Turkey +, Prov. +Siirt +, +Kusgunkiran Ģeçidi +, + +1.vi.1989 + +, leg. +A. Podlussány’ + +; + +1 female +( +ZIN +): ‘ +Turkey, TR +06-34, +Muş +, +Hwy +959, +Otluk Dağları +, + +41.7 km + +ENE of +Muş +, 38˚52'13.0" 41˚56'33.8" + +1740 13.vi. + +2006, +A. Konstantinov +leg. + +’. + + + + \ No newline at end of file diff --git a/data/38/57/BD/3857BD64FFA1FFDBFF6C4F934B9DFB38.xml b/data/38/57/BD/3857BD64FFA1FFDBFF6C4F934B9DFB38.xml new file mode 100644 index 00000000000..9a61b221ed1 --- /dev/null +++ b/data/38/57/BD/3857BD64FFA1FFDBFF6C4F934B9DFB38.xml @@ -0,0 +1,250 @@ + + + +Contribution to the taxonomy and nomenclature of Entiminae from the Palaearctic region and South Africa (Coleoptera: Curculionidae) + + + +Author + +Yunakov, N. N. + + + +Author + +Klass K. D. + +text + + +Beiträge Zur Entomologie = Contributions to Entomology + + +2012 + +2012-12-20 + + +62 + + +2 + + +427 +445 + + + + +https://www.contributions-to-entomology.org/article/view/1825 + +journal article +2560 +10.21248/contrib.entomol.62.2.427-445 +97bcdde4-9fc2-4696-9d82-7a0a5e2be65f +0005-805X +4779554 + + + + + + + +Chiloneus +SCHOENHERR, 1842: 234 + + + + + + + +[ +type +species: + +Chiloneus siculus +Boheman, 1842 + +, by original designation] + + + + + +Chilonorrhinus +Reitter, 1915: 187 + +, +syn. n. + + +[ +type +species: + +Chilonorrhinus sitonoides +Reitter, 1915 + +, here designated] + + + + +Taxonomic notes: + + + +Chiloneus + +includes 46 species distributed over the Mediterranean region. + +Chilonorrhinus + +includes 4 species from +Algeria +, +Italy +, +Greece +, and +Israel +. +Reitter (1915b) +established + +Chilonorrhinus + +only based on the shape of scales (piliform, vs broad in + +Chiloneus + +). Head shape, the proportions of the body, and the structure of the frontoepistome are very similar in + +Chilonorrhinus + +and + +Chiloneus + +. Our examinations suggest that the +type +species + +Chilonorrhinus sitonoides + +differs from + +Chiloneus +species + +only by having piliform hairs in its vestiture and a fine punctuation of the pronotum ( +Fig. 9 +). Difference of this kind are not significant enough to separate species at genus level. The female genitalia are very similar in + +Chilonorrhinus sitonoides + +and most + +Chiloneus +species. + +We consider this sufficient reason to transfer + +Chilonorrhinus sitonoides + +to + +Chiloneus + +. The other three + +Chilonorrhinus +species + +(which we did not examine) are also transferred to + +Chiloneus + +, as there is no evidence in favour of their separation from + +Chilonorrhinus sitonoides + +at genus level. The following new combinations are thus proposed: + +Chiloneus sitonoides +(Reitter, 1915) + +, +comb. n. +, + +Chiloneus aliquoi +(Pesarini, 1974) + +, +comb. n. +, + +Chiloneus corcyreus +(Penecke, 1935) + +, +comb. n. +, and + +Chiloneus sahlbergi +(Reitter, 1915) + +, +comb. n. + + + + + +Type +material: + + + + + +C. sitonoides + +( +Figs 9-13 +): +Holotype +, +female +( +MTMB +): ‘Algier, Reitter (Leder) [printed] / X.p.g. + +Sciaphilus + +’ [hand written] / + +Desbrochersella sitonoides + +m in lit. [hand written by E. Reitter] / + +Chilonorrhinus sitonoides + +m. Type, 1915 [hand written by E. Reitter] / coll. +Reitter +[printed] / Monotypus + +Chilonorrhinus sitonoides +Reitter, 1915 + +’ [hand written label with red frame]. + + + + + \ No newline at end of file diff --git a/data/38/57/BD/3857BD64FFABFFD1FF6C4CEA4980FD1A.xml b/data/38/57/BD/3857BD64FFABFFD1FF6C4CEA4980FD1A.xml new file mode 100644 index 00000000000..29eef0fab09 --- /dev/null +++ b/data/38/57/BD/3857BD64FFABFFD1FF6C4CEA4980FD1A.xml @@ -0,0 +1,75 @@ + + + +Contribution to the taxonomy and nomenclature of Entiminae from the Palaearctic region and South Africa (Coleoptera: Curculionidae) + + + +Author + +Yunakov, N. N. + + + +Author + +Klass K. D. + +text + + +Beiträge Zur Entomologie = Contributions to Entomology + + +2012 + +2012-12-20 + + +62 + + +2 + + +427 +445 + + + + +https://www.contributions-to-entomology.org/article/view/1825 + +journal article +2560 +10.21248/contrib.entomol.62.2.427-445 +97bcdde4-9fc2-4696-9d82-7a0a5e2be65f +0005-805X +4779554 + + + + + + + +Ellimenistes +BOHEMAN + +in SCHOENHERR C. J. 1843 + + + + + + + +Pimelorrhinus +Reitter, 1915: 116 + +, +syn. n. + + + + \ No newline at end of file diff --git a/data/38/57/BD/3857BD64FFABFFD1FF6C4D564995F9BF.xml b/data/38/57/BD/3857BD64FFABFFD1FF6C4D564995F9BF.xml new file mode 100644 index 00000000000..5af2aa1e2bc --- /dev/null +++ b/data/38/57/BD/3857BD64FFABFFD1FF6C4D564995F9BF.xml @@ -0,0 +1,206 @@ + + + +Contribution to the taxonomy and nomenclature of Entiminae from the Palaearctic region and South Africa (Coleoptera: Curculionidae) + + + +Author + +Yunakov, N. N. + + + +Author + +Klass K. D. + +text + + +Beiträge Zur Entomologie = Contributions to Entomology + + +2012 + +2012-12-20 + + +62 + + +2 + + +427 +445 + + + + +https://www.contributions-to-entomology.org/article/view/1825 + +journal article +2560 +10.21248/contrib.entomol.62.2.427-445 +97bcdde4-9fc2-4696-9d82-7a0a5e2be65f +0005-805X +4779554 + + + + + + + +Ellimenistes setulosus +FÅHRAEUS +, 1871 + + + + + + + + +Pimelorrhinus globatus +Reitter, 1915 + +, + +syn. n. + + + + + +Taxonomic notes: + + +The original description of + +Pimelorrhinus + +and of its sole species + +P. globatus + +was based on a single male ( +Fig. 1 +) with the label ‘Ins. Rhodus’ ( +Fig. 2 +). No further species were assigned later to + +Pimelorrhinus + +, so that the genus has remained monotypic. +Reitter (1915a) +attributed + +Pimelorrhinus + +to the tribe +Holcorrhinini +because it shares with those a transversal sulcus on the epifrons beyond the eyes. In fact, the +type +specimen must be transferred to the South African genus + +Ellimenistes +Boh. + +, of which 36 species have become described. Moreover, there are no differences in external morphology and male genitalia between the +type +specimen of + +Pimelorrhinus globatus +Rtt. + +and + +Ellimenistes setulosus +Fåhr. Thus + +, a new synonymy is proposed here for + +Ellimenistes setulosus +Fåhraeus, 1871 + +and + +Pimelorrhinus globatus +Reitter, 1915 + +. + + +‘Ins. Rhodus’ could be interpreted as the +Dodecanese +island in +Aegean +Sea bearing this name. However, there is no further record for either name from the Mediterranean region. Thus either the “ + +Pimelorrhinus globatus + +” specimen was introduced to this island accidentally, or the specimen is mislabeled. One possible source for mislabeling is the similarity of spelling of ‘Rhodus’ and ‘Rhodes’, a university in Grahamstown (established in 1904) in the Eastern Cape province, where + +Ellimenistes setulosus + +was described from ( +Fåhraeus 1871 +). + + + + + +Type +material: + + + + +Pimelorrhinus globatus + +: + +Holotype +, male ( +MTMB +): ‘Ins. Rhodus’ / ‘ +Pimelorrhinus globatus +m. 1915. Type’ / ‘Coll. Reitter’ / ‘Monotypus +Pimelorrhinus globatus Reitter 1915 +’ / ‘ +Ellimenistes setulosus Fåhr., Yunakov +det. 2009’. + + + +Other material examined: + + + +South Africa +: + + +1 ♂, 1 ♀ ( +MTMB +) “S. Africa/ Natal”; + + +1 ♂ ( +ZIN +) “South Africa (Natal)”; + + +2 ♂♂ 1 ♀ ( +KUMN +) “Port Natal [= Durban]/ Deyrolle [leg.]” + +. + + + + \ No newline at end of file diff --git a/data/38/57/BD/3857BD64FFACFFD6FED04D614C3DFC9F.xml b/data/38/57/BD/3857BD64FFACFFD6FED04D614C3DFC9F.xml new file mode 100644 index 00000000000..53bf1bfd4fb --- /dev/null +++ b/data/38/57/BD/3857BD64FFACFFD6FED04D614C3DFC9F.xml @@ -0,0 +1,78 @@ + + + +Contribution to the taxonomy and nomenclature of Entiminae from the Palaearctic region and South Africa (Coleoptera: Curculionidae) + + + +Author + +Yunakov, N. N. + + + +Author + +Klass K. D. + +text + + +Beiträge Zur Entomologie = Contributions to Entomology + + +2012 + +2012-12-20 + + +62 + + +2 + + +427 +445 + + + + +https://www.contributions-to-entomology.org/article/view/1825 + +journal article +2560 +10.21248/contrib.entomol.62.2.427-445 +97bcdde4-9fc2-4696-9d82-7a0a5e2be65f +0005-805X +4779554 + + + + + + + +Parameira +SEIDLITZ, 1868: 26 + + + + + + + +[ +type +species: + +Stomodes rudis +Boheman, 1843 + +, by subsequent designation in +Yunakov 2004: 1284 +] + + + + \ No newline at end of file diff --git a/data/38/57/BD/3857BD64FFACFFD6FED04DED49F1F9A3.xml b/data/38/57/BD/3857BD64FFACFFD6FED04DED49F1F9A3.xml new file mode 100644 index 00000000000..a21f51f6ecb --- /dev/null +++ b/data/38/57/BD/3857BD64FFACFFD6FED04DED49F1F9A3.xml @@ -0,0 +1,328 @@ + + + +Contribution to the taxonomy and nomenclature of Entiminae from the Palaearctic region and South Africa (Coleoptera: Curculionidae) + + + +Author + +Yunakov, N. N. + + + +Author + +Klass K. D. + +text + + +Beiträge Zur Entomologie = Contributions to Entomology + + +2012 + +2012-12-20 + + +62 + + +2 + + +427 +445 + + + + +https://www.contributions-to-entomology.org/article/view/1825 + +journal article +2560 +10.21248/contrib.entomol.62.2.427-445 +97bcdde4-9fc2-4696-9d82-7a0a5e2be65f +0005-805X +4779554 + + + + + + + +Parameira +( +Lepidostomodes +) +gebleri +FAUST, 1893 + + + + + + + + + + +Parameira volgense +Korotyaev, 1992: 816 + + +, + +syn. n. + + + + +Taxonomic notes: + + + + +This species occurs in southern Ural and from +Altai +to Transbaikalia, where it appears parthenogenetic. In addition, there is a bisexual form present along Volga River (around midlength), which +Korotyaev (1992) +described as + +P. volgense +Kor. + +(compared with + +P. setosa +Seidlitz, 1868 + +instead of + +P. gebleri + +). Due to the absence of morphological differences between +type +specimens of both species, we consider + +P. volgense + +conspecific to + +P. gebleri + +. + + + + + +Type +material: + + + + +P. volgense + +: + +Holotype +, male ( +ZIN +); +Russia +, +Ul’yanovsk Prov. +, +Radischevskiy Distr. +, +Ashtala Mt. +, + +9.viii.1991 + +, +A.Yu. Isaev +leg. + + +Paratypes +: 2 ♀♀ ( +ZIN +), labeled as +holotype + +. + + +Other material examined: + + + + +Kazakhstan +: + +1 ♀ ( +SZMN +), +Akmolinsk Prov. +, +Shortandy +, + +24.vii-3.viii.1979 + +, +V. Mordkovitch +leg. + +; + +2 ♀♀ ( +SZMN +), +Akmolinsk Prov. +, +Shortandy +, + +15.vi-5.viii.1978 + +, +V. Mordkovitch +leg. + + + + + +Mongolia +: + +2 ♀♀ ( +ZIN +), +Suhbaatar +, Dzotol-Khan-Ula, + +12.vii.1971 + +, +A. F. Yemelyanov +leg. + + + + + +Russia +: + +2 ♀♀ ( +SZMN +), +Krasnoyarsk +Terr. +, +Brazhnoye +, + +v.1982 + +; + + +2 ♀♀ ( +SZMN +), +Krasnoyarsk +Terr. +, +Vladimirovka +, 19- + +22.07.1984 + +, +V. Mordkovitch +leg. + + +2 ♀♀ ( +SZMN +), +Novosibirsk +, +Chistoozernyi Distr. +, +Lake Karachi +, + +21.vi-13.vii.1970 + +, +V. Mordkovitch +leg. + + +1 ♀ ( +SZMN +), +Novosibirsk Prov. +, +Toguchinskii Distr. +, +Gornyi +, +Mt. Lysaya +, + +15.vii.1998 + +, +R. Dudko +& +A. Legalov +leg. + + +1 ♀ ( +SZMN +), +Samara Prov. +, + +13.5 km +SSW of Kostino + +, meadow, + +20-28.viii.1993 + +, +I. Smeljansky +leg.; + + +1 ♀ ( +KUMN +), +Yakutia Republic +, +Yakutsk +env., + +25.v.1980 + +, +Rentz +leg. + + + + + \ No newline at end of file diff --git a/data/38/57/BD/3857BD64FFACFFD6FED04F164C5BFD0B.xml b/data/38/57/BD/3857BD64FFACFFD6FED04F164C5BFD0B.xml new file mode 100644 index 00000000000..8fc20283ca5 --- /dev/null +++ b/data/38/57/BD/3857BD64FFACFFD6FED04F164C5BFD0B.xml @@ -0,0 +1,145 @@ + + + +Contribution to the taxonomy and nomenclature of Entiminae from the Palaearctic region and South Africa (Coleoptera: Curculionidae) + + + +Author + +Yunakov, N. N. + + + +Author + +Klass K. D. + +text + + +Beiträge Zur Entomologie = Contributions to Entomology + + +2012 + +2012-12-20 + + +62 + + +2 + + +427 +445 + + + + +https://www.contributions-to-entomology.org/article/view/1825 + +journal article +2560 +10.21248/contrib.entomol.62.2.427-445 +97bcdde4-9fc2-4696-9d82-7a0a5e2be65f +0005-805X +4779554 + + + + + + + +Otiorhynchus +( +Eunihus +) +pisidicus +(MAGNANO) + +, +comb. n. + + + + + + +Magnano, 2003: 245 +( + +Parameira + +) + + + + +Taxonomic notes: + + +When describing this species, +Magnano (2003) +assigned it to the genus + +Parameira +Seidlitz, 1868 + +, which includes 7 species distributed mostly over southern Europe and + +P. gebleri +Faust, 1893 + +from southern Siberia. Reasons for this assignment were not given. Four +paratypes +of + +Parameira pisidica + +were examined and compared both with + +Parameira +species + +and + +Otiorhynchus +( +Eunihus +) + +species. First, there are no significant differences between + +P. pisidica + +and + +Otiorhynchus +( +Eunihus +) + +. Second, + +P. pisidica + +does not show any of the significant apomorphies of + +Parameira + +, such as the epistomal carina surrounding the epistome and the posterior squamulate fringe of the pronotum. Its elytra are pyriform as in + +Eunihus + +but not oblong-ovate as in + +Parameira + +. + + + + \ No newline at end of file diff --git a/data/38/57/BD/3857BD64FFADFFD4FF6C4A2F4BDCFE34.xml b/data/38/57/BD/3857BD64FFADFFD4FF6C4A2F4BDCFE34.xml new file mode 100644 index 00000000000..bb7be59831c --- /dev/null +++ b/data/38/57/BD/3857BD64FFADFFD4FF6C4A2F4BDCFE34.xml @@ -0,0 +1,269 @@ + + + +Contribution to the taxonomy and nomenclature of Entiminae from the Palaearctic region and South Africa (Coleoptera: Curculionidae) + + + +Author + +Yunakov, N. N. + + + +Author + +Klass K. D. + +text + + +Beiträge Zur Entomologie = Contributions to Entomology + + +2012 + +2012-12-20 + + +62 + + +2 + + +427 +445 + + + + +https://www.contributions-to-entomology.org/article/view/1825 + +journal article +2560 +10.21248/contrib.entomol.62.2.427-445 +97bcdde4-9fc2-4696-9d82-7a0a5e2be65f +0005-805X +4779554 + + + + + + +Subgenus + +Eudipnus +C. G. THOMSON, 1859 + + + + + + + +[ +type +species: + +Curculio micans +Fabricius, 1792 + +(= + +C. mollis +Ström, 1768 + +)] + + + + + +Eudipnoidius +Apfelbeck, 1898 + +, +syn. n. + + +[ +type +species: + +Polydrosus sciaphiliformis +Apfelbeck, 1898 + +by monotypy] + + + + +Taxonomic notes: + + +Apfelbeck (1898) +erected the subgenus + +Eudipnoidius + +for + +Polydrusus sciaphiliformis + +solely on the basis that + +Eudipnoidius + +has weaker humeral processes on the elytra than + +Polydrusus + +, and he suggests + +Eudipnoidius + +to be placed in between the genera + +Sciaphobus + +(with reduced humeral processes correlated with lack of hind wings) and + +Polydrusus + +(with strongly developed humeral processes correlated with complete hind wings). All significant characters traditionally used for discriminating subgenera within + +Polydrusus + +(structure and shape of rostrum parts, position and shape of hypostomal-labial sutures and posterior tentorial pit, and also features of leg shape) are identical with + +Polydrusus +( +Eudipnus +) + +. We thus synonymise + +Eudipnoidius + +with + +Eudipnus + +. This is based on examination of +one female +syntype +and one recently collected male of + +P. sciaphiliformis +Apfb. Both + +specimens are very similar to + +P. +( +Eudipnus +) +lateralis +Gyll. + +, + +P. +( +E. +) +cocciferae +Kiesw. + +and + +P. +( +E. +) +mollis +(Ström) + +in external morphology and genitalia structure of both sexes. +P. sciaphiliformis +differs from these species only in the shape of the scales of body vestiture and in the shape of the apex of the median lobe, while the internal sac armature and aggonoporium are almost identical. + + + + + +Type +material: + + + + + +Polydrosus sciaphiliformis + +: + +Bulgaria + +: +female +, +syntype +( +MTMB +), ‘Sofia, Vitosa pl + +.’. + + +Other material examined: + + + +Polydrosus sciaphiliformis + +: + + +Greece + +: 1 ♂ ( +MTMB +), ‘Greece, Trakia, Megalo Dereio, +25.v.2004 +, S. Ilniczky leg + +.’ / ‘ + +Polydrosus sciaphiliformis + +Apfelbeck, 1898 +Yunakov + + +det. 2009’. + + + + +Polydrosus lateralis + +: + +Greece + +: 2 ♂♂, 2 ♀♀ ( +ZIN +) ‘Thrakia’; + + +1 ♂, 1 ♀ ( +ZIN +) ‘Attica’. + + + + + \ No newline at end of file diff --git a/data/38/57/BD/3857BD64FFADFFD7FF6C4ED94BF5FC26.xml b/data/38/57/BD/3857BD64FFADFFD7FF6C4ED94BF5FC26.xml new file mode 100644 index 00000000000..cd1c427794f --- /dev/null +++ b/data/38/57/BD/3857BD64FFADFFD7FF6C4ED94BF5FC26.xml @@ -0,0 +1,169 @@ + + + +Contribution to the taxonomy and nomenclature of Entiminae from the Palaearctic region and South Africa (Coleoptera: Curculionidae) + + + +Author + +Yunakov, N. N. + + + +Author + +Klass K. D. + +text + + +Beiträge Zur Entomologie = Contributions to Entomology + + +2012 + +2012-12-20 + + +62 + + +2 + + +427 +445 + + + + +https://www.contributions-to-entomology.org/article/view/1825 + +journal article +2560 +10.21248/contrib.entomol.62.2.427-445 +97bcdde4-9fc2-4696-9d82-7a0a5e2be65f +0005-805X +4779554 + + + + + +3.3. Tribe + +Polydrusini +SCHOENHERR, 1823 + + + + + + +According to traditional systematics +Polydrusini +comprises the genera with following superficial morphological characters: + +1) antennal scrobes strictly lateral, with well developed edges; +2) pronotum without vibrissae at the sides of the anterior margin; +3) humeral prominences on elytra developed; + +4) setal comb of hind tibiae, simple or with inner bare ridnge, additional comb always absent ( +Fig. 26 +); + +5) setal comb of hind tibiae stricted by apical edge of tibia and not continuing on its dorsal edge; 6) claws connate. + +Old and recent data have revealed many exceptions in character 3 within genera being considered in +Polydrusini +: + +Liophloeus +Germar, 1817 + +, + +Metadrosus +Schilsky, 1910 + +, + +Homapterus +Fairmaire, 1857 + +, + +Synaptorhinus +Faust, 1889 + +(new placement), and + +Polydrusus + +subgenera + +Orodrusus +Korotyaev et Meleshko, 1997 + +, + +Scythodrusus +Korotyaev et Meleshko, 1997 + +, + +Leucodrusus + +, and + +Eudipnus + +when humeral processes are more or less reduced ( +Smreczyński 1958 +; +Borovec & Fremuth 2000 +; original data of authors). That was expectable as aptery is already described in +Phyllobiini +and +Cyphicerini +( +Korotyaev & Egorov 1977 +; +Morimoto et al. 2006 +). + + +Tribal relationships and phylogenetic pattern of +Polydrusini +genera are not studied yet. A hypoth-hypothesis on the relationship of +Polydrusini +with +Phyllobiini +was proposed ( +Zherikhin & Egorov 1991 +) because of similarity in general appearance, structure of thorax, limbs, and wing venation, but simultaneously significant differences were highlighted in structure of antennal socets, antennae, shape. Recently Japanese experts, supporting Zherikhins’s opinion, descovered other defferences of +Polydrusini +from +Phyllobiini +: absence of denticles on medial edge of deciduous mandibular process (without denicles) and presence of styli on coxites of ovipositor ( +Morimoto et al. 2006 +). The statement on the presence of styli in all +Polydrusini +is not confirmed by our recent unpublished study of + +Polydrusus + +subgenera + +Scythodrusus + +and + +Orodrusus + +. + + + + \ No newline at end of file diff --git a/data/38/57/BD/3857BD64FFAEFFD4FED04C474BDFFB30.xml b/data/38/57/BD/3857BD64FFAEFFD4FED04C474BDFFB30.xml new file mode 100644 index 00000000000..474ce7c46e8 --- /dev/null +++ b/data/38/57/BD/3857BD64FFAEFFD4FED04C474BDFFB30.xml @@ -0,0 +1,191 @@ + + + +Contribution to the taxonomy and nomenclature of Entiminae from the Palaearctic region and South Africa (Coleoptera: Curculionidae) + + + +Author + +Yunakov, N. N. + + + +Author + +Klass K. D. + +text + + +Beiträge Zur Entomologie = Contributions to Entomology + + +2012 + +2012-12-20 + + +62 + + +2 + + +427 +445 + + + + +https://www.contributions-to-entomology.org/article/view/1825 + +journal article +2560 +10.21248/contrib.entomol.62.2.427-445 +97bcdde4-9fc2-4696-9d82-7a0a5e2be65f +0005-805X +4779554 + + + + + + +Subgenus + +Eustolus +C. G. THOMSON, 1859 + + + + + + + +[type species: + +Curculio flavipes +DeGeer, 1775 + +] + + + + + + + +Tylodrusinus +Reitter, 1916: 56 + + +, +syn. n. + + + +[type species: + +Polydrusus julianus +Reitter, 1916 + +] + + + + +Taxonomic notes: + + +Reitter (1916) +erected the subgenus + +Tylodrusinus + +for the single species + +Polydrusus julianus + +from the +Xinjiang province +of +China +( +Figs 3, 4 +). In general appearence its +holotype +differs from species of the subgenus + +Eustolus + +basically by the vestigial rather than extensive condition of shining metallic scales on the body. E. Reitter stressed this difference in the original description but did not provide any other significant evidence for the discrimination of + +Tylodrusinus + +. The structure of the head, pronotum, elytra, legs and abdomen agrees with that in + +Eustolus + +. There are no other particular characters suggesting + +Tylodrusinus + +to be classified as a distinct subgenus. Therefore + +P. julianus +Rtt. + +is here transferred to the subgenus + +Eustolus +C. G. Thomson, 1859 + +. In a discussion of this topic Dr. B. A. Korotyaev has agreed upon this synonymy. + + +Lectotype +designation is required and here done because the original description was based on several specimens. + + + + +Type material: + + + +Polydrusus julianus + +: + +Lectotype +, +female +here designated +( +MTMB +): ‘Turkestan [printed]’ / ‘Kuldscha [printed]’ / ‘Kuldscha [hand written]’ / ‘julianus m. Fn. Grm V. [hand written]’ / ‘Coll. +Reitter +[printed] + +’ / ‘ + +Holotypus + +Polydrusus julianus + +Reitter +, 1916 + + +[standard museum label in red frame]’ / ‘Lectotype + +Polydrusus julianus +Reitter, Yunakov + +des., 2009 [red, printed]’. + + + + + \ No newline at end of file diff --git a/data/38/57/BD/3857BD64FFAEFFD5FED04BE649B9FE3C.xml b/data/38/57/BD/3857BD64FFAEFFD5FED04BE649B9FE3C.xml new file mode 100644 index 00000000000..061e2179fb2 --- /dev/null +++ b/data/38/57/BD/3857BD64FFAEFFD5FED04BE649B9FE3C.xml @@ -0,0 +1,140 @@ + + + +Contribution to the taxonomy and nomenclature of Entiminae from the Palaearctic region and South Africa (Coleoptera: Curculionidae) + + + +Author + +Yunakov, N. N. + + + +Author + +Klass K. D. + +text + + +Beiträge Zur Entomologie = Contributions to Entomology + + +2012 + +2012-12-20 + + +62 + + +2 + + +427 +445 + + + + +https://www.contributions-to-entomology.org/article/view/1825 + +journal article +2560 +10.21248/contrib.entomol.62.2.427-445 +97bcdde4-9fc2-4696-9d82-7a0a5e2be65f +0005-805X +4779554 + + + + + + + +Polydrusus impar +GOZIS, 1882 + + + + + +vranicensis +Reitter, 1905: 247 +, + +syn. n. + + + + + +Taxonomic notes: + + +According to ICZN (article 45.6.4), + +Polydrusus impar +var. +vranicensis + +has to be treated as subspecies. The +type +locality is in Bosnian highlands, where this form occurs in the subalpine zone. The specimens differ from the common appearance of + +P. impar + +only in the absence of scales with metallic shine in the body vestiture, as also mentioned by E. Reitter in the original descrip-description. A reduction of scales with metallic shine in the vestiture is very common among +Entiminae +groups in which the vestiture usually contains such scales. For example, complete reduction of such scales can be observed in some specimens of + +Polydrusus amoenus +Germar, 1824 + +, + +Phyllobius pomaceu + +s Gyllenhal, 1834, and + +Ph. glaucus +(Scopoli, 1763) + +. There are no other morphological reasons to discriminate + +P. impar vranicensis + +from typical specimens of + +P. impar + +, which occur in Vranice Planina, too. + + + + +Type material: + + + +Syntypes +, +2 females +( +MTMB +), ‘‘ +Bosnia Bosnia +, +Vranice Pl. +’ / ‘ ‘leg leg. +Leonhard’ +/ ‘ ‘ MetallitesMetallites +impar v. vranicensis +m. [Reitter’s hand writing] + +’. + + + + \ No newline at end of file diff --git a/data/38/57/BD/3857BD64FFAFFFD5FF6C4C3C4B50FD4B.xml b/data/38/57/BD/3857BD64FFAFFFD5FF6C4C3C4B50FD4B.xml new file mode 100644 index 00000000000..f7061c41a3c --- /dev/null +++ b/data/38/57/BD/3857BD64FFAFFFD5FF6C4C3C4B50FD4B.xml @@ -0,0 +1,78 @@ + + + +Contribution to the taxonomy and nomenclature of Entiminae from the Palaearctic region and South Africa (Coleoptera: Curculionidae) + + + +Author + +Yunakov, N. N. + + + +Author + +Klass K. D. + +text + + +Beiträge Zur Entomologie = Contributions to Entomology + + +2012 + +2012-12-20 + + +62 + + +2 + + +427 +445 + + + + +https://www.contributions-to-entomology.org/article/view/1825 + +journal article +2560 +10.21248/contrib.entomol.62.2.427-445 +97bcdde4-9fc2-4696-9d82-7a0a5e2be65f +0005-805X +4779554 + + + + + + +Subgenus + +Eurodrusus +KOROTYAEV +et MELESHKO, 1997 + + + + + + + +[ +type +species: + +Polydrusus confluens +Stephens, 1831 + +, by original designation] + + + + \ No newline at end of file diff --git a/data/38/57/BD/3857BD64FFAFFFD5FF6C4CAE488FFB06.xml b/data/38/57/BD/3857BD64FFAFFFD5FF6C4CAE488FFB06.xml new file mode 100644 index 00000000000..2d80baa5f00 --- /dev/null +++ b/data/38/57/BD/3857BD64FFAFFFD5FF6C4CAE488FFB06.xml @@ -0,0 +1,161 @@ + + + +Contribution to the taxonomy and nomenclature of Entiminae from the Palaearctic region and South Africa (Coleoptera: Curculionidae) + + + +Author + +Yunakov, N. N. + + + +Author + +Klass K. D. + +text + + +Beiträge Zur Entomologie = Contributions to Entomology + + +2012 + +2012-12-20 + + +62 + + +2 + + +427 +445 + + + + +https://www.contributions-to-entomology.org/article/view/1825 + +journal article +2560 +10.21248/contrib.entomol.62.2.427-445 +97bcdde4-9fc2-4696-9d82-7a0a5e2be65f +0005-805X +4779554 + + + + + + + +Polydrusus cervinus +(LINNAEUS, 1758) + + + + + +Taxonomic notes: + + + + + +Polydrusus cervinus + +is a highly variable species with a huge distribution range over the whole of Europe. Members of this species were described for many times. Here the type series of + +P. iris + +, already proposed to be a synonym of + +P. cervinus +( +Dalla Torre et al., 1936 +) + +, is critically examined. It consists of +three syntypes +obviously belonging to two different species, + +Polydrusus cervinus + +and + +Pachyrhinus mustela +(Herbst, 1797) + +. This situation requires a +lectotype +designation of + +Curculio iris + +for the sake of stability of nomenclature. + + + + +Type material: + + + +Lectotype +, +male +, +here designated +( +ZMUC +): ‘iris’, ‘Lectotypus + +Curculio iris +Fabricius Yunakov + +des. 2010’, ‘ + +Polydrusus cervinus + +(L.) +Yunakov +det.’ + +. + +Paralectotypes +: 1 ♀ ( +ZMUC +), ‘iris’, ‘Paralectotypes + +Curculio iris +Fabricius Yunakov + +des. 2010’, ‘ + +Polydrusus cervinus + +(L.) Yunakov det.’; + + +1 ♀ (ZMUC), ‘iris’, ‘Paralectotypes + +Curculio iris +Fabricius Yunakov + +des. 2010’, ‘ + +Pachyrhinus mustela +(Hbst.) +Yunakov + +det.’. + + + + + \ No newline at end of file diff --git a/data/38/57/BD/3857BD64FFAFFFDBFF6C4B7B4C35FE58.xml b/data/38/57/BD/3857BD64FFAFFFDBFF6C4B7B4C35FE58.xml new file mode 100644 index 00000000000..b50a6927369 --- /dev/null +++ b/data/38/57/BD/3857BD64FFAFFFDBFF6C4B7B4C35FE58.xml @@ -0,0 +1,316 @@ + + + +Contribution to the taxonomy and nomenclature of Entiminae from the Palaearctic region and South Africa (Coleoptera: Curculionidae) + + + +Author + +Yunakov, N. N. + + + +Author + +Klass K. D. + +text + + +Beiträge Zur Entomologie = Contributions to Entomology + + +2012 + +2012-12-20 + + +62 + + +2 + + +427 +445 + + + + +https://www.contributions-to-entomology.org/article/view/1825 + +journal article +2560 +10.21248/contrib.entomol.62.2.427-445 +97bcdde4-9fc2-4696-9d82-7a0a5e2be65f +0005-805X +4779554 + + + + + + + +Synaptorhinus +FAUST, 1889 + +(new placement) + + + + + + +[ +type +species: + +Synaptorhinus simplex +Faust, 1889 + +, by monotypy] + + + + +This poorly-known monotypic genus was erected for + +S. simplex +Faust, 1889 + +from +Turkey +. The original description in Faust (1889) is fairly incomplete, and we thus provide a redescription that includes the morphological details required for comparison with resembling +Entiminae +genera. + + +Redescription: + + +Measurements. +Body length +4 mm +, width +2.2 mm +. +V +estiture and coloration. +Head and body densely covered with round, gold-cupreous scales with slightly pronounced pearl shine. Frontoepistome covered with scattered scales ( +Figs 14, 15 +). Antennal scape sparsely covered with slender recumbent and suberect scales; funicle without recumbent scales. Intervals between elytral striae weakly convex, covered with spatulate suberect scales. Light scales form an indistinct pattern of small blurs on the elytra. + + +Head +( +Figs 16-18 +, +23 +) + + +Compound eyes small, strongly and irregularly convex, their maximum width situated posteriad of their midlength. Epifrons distinctly narrowed apically, flat. Epistome and frons fused into a frontoepistome; this is coarsely punctate. Epistome with a pair of setae. Frons with weakly developed setal row. Frontoepistome demarcated from epifrons by scattered scales; U-shaped sharp carina not developed. Anterior margin of clypeus bare, without comb of microscopic setae. +Ventral side of head +( +Fig. 24 +): Prementum broad, rounded, entirely covering buccal cavity, with one pair of setae. Labial palps entirely hidden. Postgenae strongly protruding. Hypostomolabial sutures completely separated and reduced to small pits. +Antennae +: Robust. Scape evenly but weakly S-shaped and widened apically, 1 +st +funicular segment 1.5x as long as 2 +nd +; rest of segments weakly rounded, slightly oblong to as long as wide; club ovate, compact, with fused segments, distinctly bordered from funicle. + + +Thorax: + + +Pronotum transverse (PL/PW=0.85), strongly rounded at the sides, widest in posterior half; at posterior margin 1.34x as wide as at anterior margin; its disk weakly and evenly convex longitudinally and transversely ( +Fig. 21 +). +Legs +: Femora obtuse, moderately swollen in middle part. Hind tibiae with simple corbels ( +Fig. 26 +). Fore tibiae widened externally ( +Fig. 19 +). Fore and middle tibiae slightly mucronate. Hind tibiae with mucro vestigial ( +Fig. 28 +). Tibial spurs absent. + + +Abdomen: + + +Anal ventrite sharply triangular, its apical edge narrowly rounded, sternite 8 with plate triangular and densely setose ( +Fig. 25 +). Tergite 6 sharply sinuate at the apex ( +Fig. 30 +). + + +Genital structures +( +Figs 29, 31-33 +) + +Ovipositor flattened; coxite divided in two sclerites; well developed stick-shaped styli. In spermatheca, ramus and collum very small. Spiculum ventrale with lamella rounded and heavily sclerotized, its anterior margin densely setose; apodeme thick with small caput developed. + + + +Diagnosis and implications on systematic position: + + + +Synaptorhinus + +was commonly attributed to (or associated with members of) + +Brachyderini ( +Dalla Torre et al. 1936 +) + +or + +Sciaphilini ( +Alonso-Zarazaga & Lyal 1999 +) + +but either placement may be inadequate as it lacks the typical autapomorphies most of +Sciaphilini +genera (epistome demarcated from frons by a sharp V-shaped ridge, frontoepistome convex or demarcated from epifrons by U- or V-shaped ridge; except of + +Euidosomus +Reitter, 1904 + +) and +Brachyderini +(anterior margin of clypeus with a comb of microscopic setae). + + + +Synaptorhinus + +also resembles the +Cneorhinini +genera + +Attactagenus +Tournier, 1876 + +, + +Philopedon +Schoenherr, 1826 + +, and particularly + +Sericopholus +Desbrochers, +1893 + +in general appearance and the triangular shape of the anal ventrite. However, + +Synaptorhinus + +lacks the significant autapomor-autapomorphies of +Cneorhinini +, which are the presence of an additional setal comb on the hind tibiae (the corbel) and a transversal sulcus separating the epifrons from the remaining head capsule. + + +On the other hand, + +Synaptorhinus + +has strongly protruding postgenae, which likely is an autapomorphy of the + +Polydrusus + +subgenus + +Eudipnus + +in +Polydrusini +. + +Synaptorhinus + +is particularly similar to + +P. +( +E. +) +lucianae +Francia +, +1985 + +in the shape of the head and eyes. On this basis we tentatively place + +Synaptorhinus +Fst. + +in the tribe +Polydrusini +, near + +Eudipnus + +. It differs from all + +Eudipnus + +species by the lack of a frontal fovea and complex of reductions due to the aptery sindrome: reduction of scutellum and humeral processes of elytra. + + + + + +Type +material: + + + + +Turkey + +: + +Lectotype +, +female +, +here designated +( +MTD +), with labels: gold board; ‘ +Asia minor +, Pipitz’; ‘Lectotypus + +Synaptorhinus simplex +Faust, +Yunakov + +des., 2009’. + + +Paralectotype +, +female +( +MTD +) with the same labels as in lectotype; ‘Paralectotypus + +Synaptorhinus simplex +Faust, +Yunakov + +des., 2009’. + + + + + \ No newline at end of file diff --git a/data/38/57/D7/3857D7600072AB67FF1DFDE9FBDA8F8E.xml b/data/38/57/D7/3857D7600072AB67FF1DFDE9FBDA8F8E.xml new file mode 100644 index 00000000000..6bb2c61f65f --- /dev/null +++ b/data/38/57/D7/3857D7600072AB67FF1DFDE9FBDA8F8E.xml @@ -0,0 +1,90 @@ + + + +Validation of certain family, generic and species names in Krapp-Schickel & Müller, 2011 and Lowry & Myers, 2013 + + + +Author + +Lowry, J. K. + +text + + +Zootaxa + + +2013 + +3731 + + +3 + + +399 +400 + + + +journal article +10.11646/zootaxa.3731.3.11 +620487c5-706f-4dd1-a052-ba001e79d48c +1175-5326 +218925 +2BB45C7C-B79D-4E5C-8A82-D080086FCD02 + + + + + + +Maeridae Krapp-Schickel, 2008 + + + + + + +Elasmopus +A. Costa, 1853 + + + + + + + + +Elasmopus polynesus + +sp. nov. +Krapp-Schickel & Müller + + + + + + +Type +material. + +Holotype +male +4.5 mm +, Bora Bora near Vaitape, fringe of coral reef, dead corals, covered with algae and sponges, +0.5–2 m +depth, +27 February–6 March 1988 +, coll. H.-G. Müller; MVRCr 462, 7217–7220 slides, remaining parts in alcohol. + + + + +Remarks. +See Krapp-Schickel & Müller (2011) for full description of the species. + + + + \ No newline at end of file diff --git a/data/38/57/D7/3857D7600072AB67FF1DFED4FDB08E05.xml b/data/38/57/D7/3857D7600072AB67FF1DFED4FDB08E05.xml new file mode 100644 index 00000000000..57dcbda1904 --- /dev/null +++ b/data/38/57/D7/3857D7600072AB67FF1DFED4FDB08E05.xml @@ -0,0 +1,75 @@ + + + +Validation of certain family, generic and species names in Krapp-Schickel & Müller, 2011 and Lowry & Myers, 2013 + + + +Author + +Lowry, J. K. + +text + + +Zootaxa + + +2013 + +3731 + + +3 + + +399 +400 + + + +journal article +10.11646/zootaxa.3731.3.11 +620487c5-706f-4dd1-a052-ba001e79d48c +1175-5326 +218925 +2BB45C7C-B79D-4E5C-8A82-D080086FCD02 + + + + + + + +Kairos segregans + +sp. nov. +Krapp-Schickel & Müller + + + + + + + +Type +material. + +Holotype +male, +3 mm +, Bora Bora, Society Islands, Matira Beach, from dead coral blocks in lagoon, +0.5– 2 m +depth, +March 1988 +. One slide: MVRCr 7225, remaining parts in alcohol. + + + + +Description. +With characters of the genus. + + + + \ No newline at end of file diff --git a/data/38/57/D7/3857D7600072AB67FF1DFF24FE378D18.xml b/data/38/57/D7/3857D7600072AB67FF1DFF24FE378D18.xml new file mode 100644 index 00000000000..8ff6dfff476 --- /dev/null +++ b/data/38/57/D7/3857D7600072AB67FF1DFF24FE378D18.xml @@ -0,0 +1,61 @@ + + + +Validation of certain family, generic and species names in Krapp-Schickel & Müller, 2011 and Lowry & Myers, 2013 + + + +Author + +Lowry, J. K. + +text + + +Zootaxa + + +2013 + +3731 + + +3 + + +399 +400 + + + +journal article +10.11646/zootaxa.3731.3.11 +620487c5-706f-4dd1-a052-ba001e79d48c +1175-5326 +218925 +2BB45C7C-B79D-4E5C-8A82-D080086FCD02 + + + + + + + +Kairos + +gen. nov. +Krapp-Schickel & Müller + + + + + + +Diagnosis. +With characters of the family. +Included species. +monotypic. + + + + \ No newline at end of file diff --git a/data/38/57/D7/3857D7600073AB66FF1DFBDCFDE68BAB.xml b/data/38/57/D7/3857D7600073AB66FF1DFBDCFDE68BAB.xml new file mode 100644 index 00000000000..d9e48715678 --- /dev/null +++ b/data/38/57/D7/3857D7600073AB66FF1DFBDCFDE68BAB.xml @@ -0,0 +1,105 @@ + + + +Validation of certain family, generic and species names in Krapp-Schickel & Müller, 2011 and Lowry & Myers, 2013 + + + +Author + +Lowry, J. K. + +text + + +Zootaxa + + +2013 + +3731 + + +3 + + +399 +400 + + + +journal article +10.11646/zootaxa.3731.3.11 +620487c5-706f-4dd1-a052-ba001e79d48c +1175-5326 +218925 +2BB45C7C-B79D-4E5C-8A82-D080086FCD02 + + + + + + +Kairosidae +fam. nov. + + + + + + + +Type +genus. + + +Kairos + + +gen. nov. + +Krapp-Schickel & Müller. + + +Diagnostic description. +Body laterally compressed. Eyes well developed, round. Antennae 1–2 calceoli absent. Antenna 1 longer than antenna 2; peduncular article 1 subequal to article 2; article 2 longer than article +3 +; article 3 shorter than article 1; peduncular articles 1–2 not geniculate. Antenna 2 peduncular article 1 not enlarged. Mandible molar triturative; palp symmetrical. Maxilla 1 basal endite apically setose; palps symmetrical. Maxilla 2 basal endite without oblique setal row. Labium inner lobes present. Coxal gills number and sequence [not known], not stalked; sternal gills absent; sternal blisters absent; oostegites fringing setae simple. Gnathopod 1 subchelate; smaller (or weaker) than gnathopod 2; propodus palm without robust setae along palmar margin. Gnathopod 2 subchelate; similar in males and females (not sexually dimorphic); carpus slightly produced along posterior margin of propodus. Pereopods 3–4 not sexually dimorphic. Pereopod 4 without posteroventral lobe. Pereopod 5 coxa with small anteroventral lobe. Pleonites 1– 3 without dorsal carinae. +Urosomites 1–2 coalesced, 3 free +; without slender or robust dorsal setae. Urosomite 1 without large distoventral robust seta. Urosomite 2 without dorsal setae. Uropod 1 without basofacial robust setae. Uropod 3 biramous, without plumose setae; endopod minute. + +Telson deeply cleft + +; dorsal or lateral robust setae absent; apical robust setae absent. + + + + +Remarks. +Kairosids are similar to the endemic Mediterranean carangoliopsids. However, carangoliopsids are subcylindrical amphipods with very small, discontiguous coxae, with gnathopod 2 dissimilar in form between males and females, with the carpus of gnathopod 1 shorter than the propodus, with well developed dactyli on the pereopods, with a relatively short merus on pereopod 3 and 4, with non-coalesced urosomites, with styliform rami on uropods 1 and with a basofacial robust seta on the peduncle of uropod 1. + + +Habitat. +Marine, epigean. + + + + +Included genera. + +Kairos + + +gen. nov. + +Krapp-Schickel & Müller. + + + + +Distribution. +Society Islands. + + + + \ No newline at end of file diff --git a/data/38/58/27/3858272ED7D954CE84AF1829E15B635D.xml b/data/38/58/27/3858272ED7D954CE84AF1829E15B635D.xml new file mode 100644 index 00000000000..84eb76d8ee0 --- /dev/null +++ b/data/38/58/27/3858272ED7D954CE84AF1829E15B635D.xml @@ -0,0 +1,253 @@ + + + +Investigation of the Amathillopsidae (Amphipoda, Crustacea), including the description of a new species, reveals a clinging lifestyle in the deep sea worldwide + + + +Author + +Loerz, Anne-Nina +Center of Naturkunde, Universitaet Hamburg, Martin-Luther King Platz 3, 20146 Hamburg, Germany +anne-nina.loerz@uni-hamburg.de + + + +Author + +Horton, Tammy +https://orcid.org/0000-0003-4250-1068 +National Oceanography Centre, Southampton, European Way, Southampton SO 14 3 ZH, UK + +text + + +ZooKeys + + +2021 + +2021-04-14 + + +1031 + + +19 +39 + + + + +http://dx.doi.org/10.3897/zookeys.1031.62391 + +journal article +http://dx.doi.org/10.3897/zookeys.1031.62391 +1313-2970-1031-19 +D39B776A5C3D44A89009D6ECE37B0AA2 +DCE2CA785D9B5A2F9A49ECA90EDD1324 + + + + +Amathillopsis Heller, 1875 + + + + +Amathillopsis +Heller, 1875: 35. - +Stebbing 1906 +: 384. - +Gurjanova 1955 +: 209 (key). - J.L. +Barnard 1969 +: 394. - J.L. +Barnard and Karaman 1991 +: 390. + + +Acanthopleustes +Holmes, 1908: 533 ( +Acanthopleustes annectens +Holmes, 1908 by original designation). + + + +Type species. + + +Amathillopsis spinigera + +Heller, 1875 (by original designation). + + + +Diagnosis + + +(after +Lowry 2006 +). +Head +. + +Deeper than long; lateral cephalic lobe subquadrate, truncated apically; anteroventral margin straight, anteroventral margin moderately recessed, anteroventral margin moderately excavate; rostrum short or moderate length; eyes present (round or ovoid) or absent. Body smooth, or dorsally carinate. Antenna 1 subequal in length or longer than antenna 2; peduncle with sparse slender setae; peduncular article 1 shorter than or subequal to article 2; article 2 longer than article 3; article 3 shorter than article 1; accessory flagellum short or minute, 1- or 2-articulate; calceoli present. Antenna 2 medium length; peduncle with sparse slender setae or none; flagellum shorter than or as long as peduncle. + + + +Pereon +. + +Coxae 1-4 longer than broad, overlapping, coxae 1-3 or coxae 1-4 ventrally acute. Coxae 1-3 similar in size or progressively larger. Gnathopod 1 subchelate; carpus shorter than or subequal to propodus; propodus with or without peg-like robust setae along palmar margin. Gnathopod 2 subchelate; coxa smaller than but not hidden by coxa 3 or subequal to but not hidden by coxa 3; carpus short, shorter than propodus. Pereopods: some or none prehensile. Pereopod 4 coxa ventrally acute, with or without small posteroventral lobe. Pereopod 5 coxa equilobate, with posteroventral lobe or with acute posterodistal lobe; basis slightly expanded or linear. Pereopod 6 subequal in length to, or longer than pereopod 7; basis slightly expanded or linear. Pereopod 7 shorter than or subequal in length to pereopod 5; basis slightly expanded or linear. + + + +Pleon +. + +Urosomite 1 carinate, urosomites 1-2 carinate or urosomites not carinate. Uropods 1-2 apices of rami without robust setae. Telson notched, emarginate or entire; dorsal or lateral robust setae absent; apical robust setae absent. + + + +Remarks. + + +Amathillopsis + +is the type genus of the family +Amathillopsidae +and the genus has a cosmopolitan distribution ( +Wakabara and Serejo 1999 +). It currently contains 12 species, five of which are known from the Pacific, + +A. annectens + +(Holmes, 1908), + +A. australis + +Stebbing, 1883, + +A. grevei + +J.L. Barnard, 1961, + +A. takahashiae + +Tomikawa & Mawatari, 2006 and + +A. pacifica + +Gurjanova, 1955 (and the sub species + +A. pacifica margo + +J.L. Barnard, 1967),; two from the Antarctic, + +A. roroi + +Coleman & Coleman, 2008 and + +A. charlottae + +Coleman, 1998; two from the Indian Ocean, + +A. septemdentata + +Ledoyer, 1978 and + +A. comorensis + +Ledoyer, 1986; and three from the North Atlantic and Arctic, + +A. affinis + +Miers, 1881, + +A. spinigera + +Heller, 1875 and + +A. atlantica + +Chevreux, 1908. + +Amathillopsis + +is a deep-sea specialist, with the shallowest records of the large species, + +A. spinigera + +, coming from colder Arctic waters at 248 m. All other species are found at depths of 500 to 3580 m. The new species, + +A. inkenae + +, described here, provides the deepest confirmed records of an + +Amathillopsis + +to date, at 4622 m and 4844 m. Table +1 +summarises the known species in the genus along with the type locality and depth. + + + +Species. + + +Amathillopsis affinis + +Miers, 1881, + +A. annectens + +(Holmes, 1908), + +A. atlantica + +Chevreux, 1908, + +A. australis + +Stebbing, 1883, + +A. charlottae + +Coleman, 1998, + +A. comorensis + +Ledoyer, 1986, + +A. grevei + +J.L. Barnard, 1961, + +A. pacifica + +Gurjanova, 1955, + +A. pacifica margo + +J.L. Barnard, 1967, + +A. roroi + +Coleman & Coleman, 2008, + +A. septemdentata + +Ledoyer, 1978, + +A. spinigera + +Heller, 1875, + +A. takahashiae + +Tomikawa & Mawatari, 2006. + + + + \ No newline at end of file diff --git a/data/38/58/47/385847AB7D475BC1AD70BE3B55E111A1.xml b/data/38/58/47/385847AB7D475BC1AD70BE3B55E111A1.xml new file mode 100644 index 00000000000..73587b37a9d --- /dev/null +++ b/data/38/58/47/385847AB7D475BC1AD70BE3B55E111A1.xml @@ -0,0 +1,88 @@ + + + +Floristic inventory and distribution characteristics of algific talus slopes in a specific area of forest biodiversity in South Korea + + + +Author + +Lee, Jong-Won +https://orcid.org/0000-0002-8687-8396 +Korea National Arboretum, Yanggu, Republic of Korea + + + +Author + +Yun, Ho-Geun +Korea National Arboretum, DMZ Forest Biological Conservation, Yanggu-gun, Republic of Korea + + + +Author + +Hwang, Tae Young +Korea National Arboretum, DMZ Forest Biological Conservation, Yanggu-gun, Republic of Korea + + + +Author + +Kim, Kyungmin +Daoneco, Sejong-si, Republic of Korea + + + +Author + +Jung, Se-Hoon +Daoneco, Sejong-si, Republic of Korea + + + +Author + +An, Jong Bin +Korea National Arboretum, DMZ Forest Biological Conservation, Yanggu-gun, Republic of Korea +ajb8825@korea.kr + +text + + +Biodiversity Data Journal + + +2023 + +2023-12-18 + + +11 + + +113952 +113952 + + + + +http://dx.doi.org/10.3897/BDJ.11.e113952 + +journal article +http://dx.doi.org/10.3897/BDJ.11.e113952 +1314-2828-11-e113952 +5B963235F71B550FA1E3BC1F0E590B10 + + + + +Coniogramme japonica (Thunb.) Diels, 1899 + + + +Distribution +Central & S. China to North Vietnam and Temperate East Asia + + + \ No newline at end of file diff --git a/data/38/59/0F/38590F957649A788C42F37339564B3C7.xml b/data/38/59/0F/38590F957649A788C42F37339564B3C7.xml new file mode 100644 index 00000000000..fa5618e8abc --- /dev/null +++ b/data/38/59/0F/38590F957649A788C42F37339564B3C7.xml @@ -0,0 +1,100 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828--9042 + + + + +Dirophanes maculicornis (Stephens, 1835) + + + + +Ichneumon maculicornis +Stephens, 1835 + + +scutellaris +(Wesmael, 1845, +Phaeogenes +) + + +bisignatus +(Holmgren, 1890, +Phaeogenes +) + + +dentatus +(Pic, 1923, +Phaeogenes +) + + +nigroscutellatus +(Habermehl, 1929, +Phaeogenes +) + + +murinanae +(Fahringer, 1936, +Microcryptus +) + + +gigas +(Fahringer, 1943, +Phaeogenes +) + + +dinianae +(Fahringer, 1948, +Phaeogenes +) + + +ruficoxis +(Constantineanu, 1959, +Phaeogenes +) preocc. + + + +Distribution +England, Scotland + + + \ No newline at end of file diff --git a/data/38/59/42/385942F0C5265C21A5F391A81ECEC515.xml b/data/38/59/42/385942F0C5265C21A5F391A81ECEC515.xml new file mode 100644 index 00000000000..fb47f878744 --- /dev/null +++ b/data/38/59/42/385942F0C5265C21A5F391A81ECEC515.xml @@ -0,0 +1,103 @@ + + + +Nomenclatural changes in Coleus and Plectranthus (Lamiaceae): a tale of more than two genera + + + +Author + +Paton, Alan J. + + + +Author + +Mwanyambo, Montfort + + + +Author + +Govaerts, Rafael H. A. + + + +Author + +Smitha, Kokkaraniyil + + + +Author + +Suddee, Somran + + + +Author + +Phillipson, Peter B. + + + +Author + +Wilson, Trevor C. + + + +Author + +Forster, Paul I. + + + +Author + +Culham, Alastair + +text + + +PhytoKeys + + +2019 + +129 + + +1 +158 + + + + +http://dx.doi.org/10.3897/phytokeys.129.34988 + +journal article +http://dx.doi.org/10.3897/phytokeys.129.34988 +1314-2003-129-1 +BF57C6B3C3065AEE9B4B3D47189C908F +3382366 + + + + +Coleus phulangkaensis (Suddee, Suphuntee & Saengrit) Suddee +comb. nov. + + + + +Plectranthus phulangkaensis +Suddee, Suphuntee & Saengrit, Thai Forest Bull., Bot. 42: 6. 2014 (Dec 2014) Type: Thailand. Nakhon Phanom, Ban Phaeng District, Phu Langka National Park, 9 Oct. 2013, Suddee, Puudjaa, Rueangruea, Kiewbang, Hemrat & Pansamrong 4588 (holotype: BKF; isotypes: BKF). + + + +Distribution. +Thailand. + + + \ No newline at end of file diff --git a/data/38/59/57/38595768E3BC69B47A8326BE66758C35.xml b/data/38/59/57/38595768E3BC69B47A8326BE66758C35.xml new file mode 100644 index 00000000000..8e238e08ac8 --- /dev/null +++ b/data/38/59/57/38595768E3BC69B47A8326BE66758C35.xml @@ -0,0 +1,73 @@ + + + +Contributions toward a reclassification of the Formicidae. Part VI. Ponerinae, tribe Ponerini, subtribe Odontomachiti. Section B. Genus Anochetus and bibliography. + + + +Author + +Brown, WL Jr., + +text + + +Studia Entomologica + + +1978 + +20 + + +549 +638 + + + + +http://antbase.org/ants/publications/6757/6757.pdf + +journal article +6757 + + + + +[38] +A. horridus + + + + +is a distinctive, gracile, testaceous species with very long, slender, sparsely toothed mandibles. The type, an ergatoid queen, was collected by Karol Lenko during our joint 1962 trip in Brasilian Amazonia, but only one of the other samples taken by our group on that excursion was mentioned by Kempf in the original description. Additional samples are from +Para +, near +Belem +: Pirelli Rubber Plantation, Iriboca (Brown). Reserva +Guama +(P. Dias). Instituto Agronomico do Norte (F. G. Werner). Amazonas, N and E of Manaus: Manaus-Itacoatiara Highway (Ruta 1), km 49 (Brown). Reserva Ducke (Brown). All localities were in lowland rain forest. + + + +Workers were found singly in leaf litter, in or under a small rotten log, and in a small nest or nest fragment in a rotten branch in the leaf litter, with larvae. + + + +Despite intensive collecting of the same kind we practiced at +Belem +and Manaus, Lenko and I failed to collect +A. horridus +during 3 weeks in the Benjamin Constant area of western Amazonas, and the species has yet to be collected in the Guyanas. + + +A. inca +, the largest of all known +Anochetus +species, remains represented in collections only by the type series, from the +Maranon +Valley in northern Peru. It seems possible that more isolated species may await discovery in other Andean valleys and foothills. + + + + \ No newline at end of file diff --git a/data/38/59/59/38595936E07DC270FC60FB84FA8FFAA6.xml b/data/38/59/59/38595936E07DC270FC60FB84FA8FFAA6.xml new file mode 100644 index 00000000000..1c6c6d3a79a --- /dev/null +++ b/data/38/59/59/38595936E07DC270FC60FB84FA8FFAA6.xml @@ -0,0 +1,79 @@ + + + +The Bivalve Cuneamya From The Late Ordovician Of Bohemia + + + +Author + +Polechová, Marika + +text + + +Fossil Imprint + + +2019 + +2019-08-29 + + +75 + + +1 + + +120 +127 + + + + +http://dx.doi.org/10.2478/if-2019-0010 + +journal article +4533 +10.2478/if-2019-0010 +06b1537b-2269-4da4-800e-3a90d8bd0cbb +2533-4069 +5384758 + + + + + + +Infraclass +Heteroconchia HERTWIG, 1895 + + + + + +Cohort Cardiomorphi FÉRUSSAC, 1822 + + + + + +Subcohort Cardioni FÉRUSSAC, 1822 (= Euheterodonta GIRIBET et DISTEL, 2003) + + + +Family +Grammysiidae MILLER, 1877 + + + + +Subfamily +Cuneamyinae MORRIS, DICKINS +et ASTAFIEVA- URBAJTIS, 1991 + + + + + \ No newline at end of file diff --git a/data/38/59/61/38596118EC1858EB9B715C3AA473C31E.xml b/data/38/59/61/38596118EC1858EB9B715C3AA473C31E.xml new file mode 100644 index 00000000000..b133687e95c --- /dev/null +++ b/data/38/59/61/38596118EC1858EB9B715C3AA473C31E.xml @@ -0,0 +1,196 @@ + + + +Five new species of the genus Hermonassa Walker, 1865 from Xizang Autonomous Region, China (Lepidoptera, Noctuidae, Noctuinae) + + + +Author + +Gao, Biao +Northeast Forestry University, School of Forestry, Harbin 150040, China + + + +Author + +Han, Hui-Lin +https://orcid.org/0000-0002-2045-6182 +Northeast Forestry University, School of Forestry, Harbin 150040, China + + + +Author + +Kononenko, Vladimir S. +https://orcid.org/0000-0001-6103-4800 +Northeast Asia Biodiversity Research Center, Northeast Forestry University, Harbin 15004, China +vsk528217@gmail.com + + + +Author + +Pan, Zhao-Hui +Northeast Forestry University, Ministry of Education, Key Laboratory of Sustainable Forest Ecosystem Management, Harbin 150040, China + +text + + +ZooKeys + + +2023 + +2023-09-08 + + +1179 + + +35 +61 + + + + +http://dx.doi.org/10.3897/zookeys.1179.107587 + +journal article +http://dx.doi.org/10.3897/zookeys.1179.107587 +1313-2970-1179-35 +D9BD50CBB127487981E99421E4F059BA +07CEAFC9849852A1AC00767783926142 + + + + + +Hermonassa oleographa Hampson, 1911 + + + + +Figs 50 +, 59 + + + + +Hermonassa oleographa +Hampson, 1911, Annals and Magazine of Natural History (8)8: 416; +Boursin 1967 +: 67; +Poole 1989 +: 503; +Plante 1994 +: 227; Yoshimoto 1994: 99, pl. 83, fig. 17; +Sugi 1995 +: 90, pl. 117, fig. 4, genit. fig. 697 ♂; +Krusek and Behounek 1996a +: pl. 51, fig. 7. + + +Hermonassa griseosignata +Chen, 1983, Acta entomologica Sinica 26(3):334, fig. 1; +Poole 1989 +: 503; +Chen et al. 1991 +: 94, pl. 4, fig. 24. + + + +Type material. + +Syntypes +: + +H. oleographa + +: [India] Sikkim, NHM [BMNH], London (not examined). +Holotype +: + +H. griseosignata + +♂ China, Xizang, Cona Magmang, 2900 m, 6 Aug. 1974, examined. + + + +Other material examined. + + +China +, +1 ♂ +, +Aut. Reg. +Xizang +, +Linzhi City +, +1-30 July 2009 +, +Z.H. Pan +leg. + +; + +1 ♂ +, +Reg. +Xizang +, +Linzhi City +, +24 Aug. 2011 +, +Z.H. Pan +leg. + +; + +5 ♂ +, +Aut. Reg. +Xizang +, +Linzhi City +, +Bomi County +, +Pailong Countryside +, +22-23 Sept. 2011 +, +H.L. Han +leg. + +, hhl-5283-1; + +6 ♂ +, +Aut. Reg. +Xizang +, +Linzhi City +, +Bomi County +, +Pailong Countryside +, +13 Sept. 2012 +, +Z.H. Pan +leg. + +, genit. prep. GB-69-1, GB-70-1 (coll. NEFU). + + + +Distribution and biology. +The species is distributed in north India (Sikkim), Nepal, Bhutan, and southwest China. In total 13 males were collected in the vicinity of Linzhi City, Prov. Xizang at altitudes of 2000-3000 m. + + + + \ No newline at end of file diff --git a/data/38/59/A7/3859A7314551FEC02CB047A752FF4BF7.xml b/data/38/59/A7/3859A7314551FEC02CB047A752FF4BF7.xml new file mode 100644 index 00000000000..78f5dd05b2b --- /dev/null +++ b/data/38/59/A7/3859A7314551FEC02CB047A752FF4BF7.xml @@ -0,0 +1,73 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828--9042 + + + + +Plectiscidea Viereck, 1914 + + + + +EPHALMATOR +Rossem, 1981 + + + +Notes + +species of +Plectiscidea +excluded from the British and Irish list: + + +[amicalis ( +Foerster +, 1871, +Plectiscus +); syn. sodalis ( +Foerster +, 1871, +Plectiscus +)] Listed as sodalis by +Fitton (1978) +, presumaby either on the basis of specimens recorded by Carr, which are not now accepted as necessarily British (see note under +Lissonota funebris +), or on the basis of specimens in BMNH identified as sodalis var. +moerens +, which is now regarded as a separate species. + + + + \ No newline at end of file diff --git a/data/38/59/B0/3859B014533EE4810FC0E846E71680BC.xml b/data/38/59/B0/3859B014533EE4810FC0E846E71680BC.xml new file mode 100644 index 00000000000..aa4e6026d02 --- /dev/null +++ b/data/38/59/B0/3859B014533EE4810FC0E846E71680BC.xml @@ -0,0 +1,60 @@ + + + +Six new deep-water sternaspid species (Annelida, Sternaspidae) from the Pacific Ocean + + + +Author + +Salazar-Vallejo, Sergio I. + + + +Author + +Buzhinskaja, Galina + +text + + +ZooKeys + + +2013 + +348 + + +1 +27 + + + + +http://dx.doi.org/10.3897/zookeys.348.5449 + +journal article +http://dx.doi.org/10.3897/zookeys.348.5449 +1313-2970-348-1 +11308C785C334B20B1C62BC4EDC52893 + + + + +Caulleryaspis Sendall & Salazar-Vallejo, 2013 + + + +Type species. + +Caulleryaspis gudmundssoni +Sendall & Salazar-Vallejo, by original designation. + + + +Diagnosis (emended). +Sternaspids with introvert hooks falcate, tapered. Pre-shield region with 7 segments. Ventro-caudal shield flexible, usually with abundant sediment particles firmly adhered, rarely sediment particles loosely adhered; without well-defined radial ribs and concentric lines. Branchial filaments arranged in discrete branchial plates. + + + \ No newline at end of file diff --git a/data/38/5A/74/385A7401545A5836A28193E6353183D2.xml b/data/38/5A/74/385A7401545A5836A28193E6353183D2.xml new file mode 100644 index 00000000000..49b3b00a1e1 --- /dev/null +++ b/data/38/5A/74/385A7401545A5836A28193E6353183D2.xml @@ -0,0 +1,97 @@ + + + +Tryphactothripini of India (Thysanoptera, Thripidae, Panchaetothripinae), with identification keys and a new record of Opimothrips + + + +Author + +Rachana, Remani R. + + + +Author + +Mound, Laurence A. + + + +Author + +Rayar, Shashikant G. + +text + + +ZooKeys + + +2019 + +884 + + +43 +52 + + + + +http://dx.doi.org/10.3897/zookeys.884.39500 + +journal article +http://dx.doi.org/10.3897/zookeys.884.39500 +1313-2970-884-43 +B0710519697244EE90C1314B3A03EEAA +36D2C73F74AF5C7FAB04D20B9E470A62 + + + + +Noathrips Bhatti, 1967 + + + + +Noathrips +Bhatti, 1967: 9. Type species +Noathrips prakashi +Bhatti, 1967 by monotypy. + + + +Notes. + +The genus was erected with the type species + +prakashi + +, collected on herbage and + +Lantana + +leaves from Jabalpur, Madhya Pradesh ( +Bhatti 1967 +). Later, this species was collected in Sri Lanka and China ( + +Kudo +1979 + +; +Xie et al. 2019 +). + + + +Diagnosis. + +Antennae 8-segmented, III and IV with forked sense cones. Head without conspicuous raised structure, postocular seta 4 strongly developed, ocellar hump small; maxillary palps bi-segmented. Pronotum with weakly raised sculpture. Mesoscutum not notched anteriorly; metascutum with prominent reticulate triangle. Tarsi 1-segmented. Fore wing with slender pointed setae; costal setae longer than fringe cilia; posteromarginal setae wavy. Abdominal tergite I with a postmarginal flange; II anterior margin constricted, with narrow plate like cuticular processes laterally; +III-VII +with transverse reticulations on anterior half, posterior half smooth; X asymmetrical, divided longitudinally. Males smaller; sternites +IV-VII +each with transversely elongated anteriorly concave pore plates. + + + + \ No newline at end of file diff --git a/data/38/5A/87/385A87FBFF929919FF6EF9B0FCEB88AA.xml b/data/38/5A/87/385A87FBFF929919FF6EF9B0FCEB88AA.xml new file mode 100644 index 00000000000..c3b5d2ab9e3 --- /dev/null +++ b/data/38/5A/87/385A87FBFF929919FF6EF9B0FCEB88AA.xml @@ -0,0 +1,1001 @@ + + + +Miyazakia, a new aphid genus from Japan (Hemiptera: Aphididae: Macrosiphini) + + + +Author + +Stekolshchikov, Andrey V. + +text + + +Zootaxa + + +2014 + +3861 + + +6 + + +575 +584 + + + +journal article +10.11646/zootaxa.3861.6.4 +c8ba0135-9d9b-4679-9643-95d86322f093 +1175-5326 +226915 +FA54C8B8-8288-462B-A553-73F1B773B06F + + + + + + + +Miyazakia + +gen. nov. + + + + + + +Type +species: + +Sappaphis ranunculi +Miyazaki, 1971 + += + +Miyazakia ranunculi +( +Miyazaki, 1971 +) + +, +comb. nov. + + + + +Description. +Body of apterous morphs elliptical or broadly elliptical, of alate morphs elliptical, elongate elliptical or elongate oval. Dorsum of apterous exules strongly sclerotized, with bands and spots fused to form a solid shield covering most of the dorsum; abdomen of other morphs with more or less clearly marked dorsal bands, sometimes fragmented on some tergites into rows of partially interconnected, partially free sclerites, and marginal maculae on all segments. Surface of head and dorsal side of body smooth, sometimes with sparse, rare, large pointed spinules, or slightly wrinkled with short rows of sparse spinules on abdominal tergites VI and VII, which on tergite VIII become more numerous and partially fused to form scales; only occasionally the surface is finely reticulate on marginal macula and around spiracles of apterous exules (contours of cells formed by thin, irregular line); surface of ventral side of abdomen with long rows of small pointed spinules sometimes forming strongly stretched cells. + + +Setae on body and appendages numerous, rigid, long, pointed or finely-pointed. Marginal and spinal tubercles present (except oviparous females). Frontal tubercles of apterous morphs are not developed, frons flat or very slightly convex. Frontal tubercles of alate morphs are well developed, the median tubercle not reaching the level of the more clearly expressed antennal tubercles. Antennae 6-segmented in all morphs except oviparous females whose antennae are 5-segmented; antennae of apterous specimens without secondary rhinaria, and alate specimens with secondary rhinaria. Secondary rhinaria round, rarely elliptical, numerous, very protruberant, with high cylindrical or slightly conical sclerotized base and membrane inflated as a dome. Ultimate rostral segment narrow, elongated, and wedge-shaped (shorter and broader in oviparous females). Legs normal. Chaetotaxy of first tarsal segments 3, 3, 2. Siphunculi are cylindrical, tapering towards the apex, with a distinct flange, sometimes slightly bottle-shaped, with long setae. Subgenital plate oval. Cauda rounded, escutcheon-like. +Hind +tibia of apterous viviparous exules and, rarely, other parthenogenetic morphs, with pheromone plates. + + + + +Etymology. +The new genus is named in honor of the well-known Japanese aphidologist Masahisa Miyazaki. Gender: feminine. + + + + +Diagnosis +. The new genus belongs to the subtribe +Anuraphidina +of tribe +Macrosiphini +(family +Aphididae +) and is related to + +Sappaphis +Matsumura, 1918 + +. Representatives of both genera have long, finely pointed setae on the body and appendages, a rounded escutcheon-like cauda, setae on the siphunculi, and a heteroecious life cycle. Apterous exules and some specimens of other parthenogenetic morphs of both genera have pheromone plates on the hind tibiae. Secondary rhinaria on the antennae of alate morphs resemble the teeth of a ripsaw (the distal edge of the sclerotized base of each rhinarium is lower than its proximal edge, so that the central axis and apex of the rhinarium is tilted toward the apex of the segment, as in the tooth of a ripsaw). + + +However, there are important differences between these genera. The dorsal setae of the body and those on appendages of + +Sappaphis + +are flagellate, whereas the corresponding setae of + +Miyazakia + +are stiff. The surface of most of the dorsum of + +Sappaphis + +is more-or-less reticulate, whereas the surface of most of the dorsal side of the body of + +Miyazakia + +is smooth with more-or-less rare spinules and only the marginal maculae of apterous exules occasionally have fine reticulation. Siphunculi of + +Sappaphis + +are without setae, except in apterous exules, where they are restricted to the flat sclerotized base or at least to the basal half; setae are present on the siphunculi of all known morphs of + +Miyazakia + +, and they are located throughout the entire length of siphunculi, or at least not confined to the basal half. The cauda of + +Sappaphis + +has numerous setae (for example 16-26 setae for apterous exules), whereas that of + +Miyazakia + +has relatively few (for example 4-7 setae for apterous exules). The primary rhinaria of +Sappaphis +are small, whereas those of + +Miyazakia + +are large with a domed projecting membrane. Apterous morphs of + +Sappaphis + +are weakly sclerotized, whereas apterous exules of + +Miyazakia + +are strongly sclerotized and have the dorsum almost covered by a solid shield, and oviparous females have more-or-less welldeveloped sclerotized bands on all tergites of thorax and abdomen. Siphunculi of apterous exules of + +Sappaphis + +are broadly conical, with an almost flat base, creating the impression that the siphunculi are located on large sclerites, whereas the siphunculi of apterous exules of + +Miyazakia + +are cylindrical or slightly bottle-shaped. The front of the head of the alate morphs of + +Sappaphis + +is slightly convex in dorsal view, whereas the frontal tubercles of the alate morphs of + +Miyazakia + +are well developed, with the median tubercle not reaching the level of the more clearly expressed antennal tubercles. The primary host of + +Sappaphis + +is pear ( + +Pyrus + +), from which aphids migrate to wormwood ( + +Artemisia + +), whereas the most probable primary host of + +Miyazakia + +is + +Photinia villosa + +, with migration to buttercup ( + +Ranunculus + +). + + +In the subtribe +Anuraphidina +, setae are also present on the siphunculi in the genera + +Sorbaphis +Shaposhnikov, 1950 + +and + +Muscaphis +Börner, 1933 + +, and in one species of + +Dysaphis +Börner, 1931 + +— + +D. sibirica +Shaposhnikov, 1986 + +. + +Miyazakia + +differs from + +Sorbaphis + +and + +Dysaphis + +by the almost complete absence of the reticulation of the cuticle, from the species of the genera + +Sorbaphis + +and + +Muscaphis + +by the presence of marginal and median tubercles and in the form of the siphunculi, and from + +Dysaphis + +by the different form of the antennal secondary rhinaria of alatae. + + + +Miyazakia ranunculi +( +Miyazaki, 1971 +) + +, +comb. nov. +( +Figs. 1–7 +, +8–18 +, +Tabl. 1–2 +) + + + + +Material examined. +Japan +: Hirao, Osaka Prefecture, + +Photinia villosa +(Thunb.) + +DC, +15.XII.1959 +(coll. M. Sorin) —2 gynoparae and +4 males +; Hirao, Osaka Prefecture, + +Rhamnus dahurica +Pall. + +, +20.XII.1959 +(coll. M. Sorin) —2 oviparous females; Taishi, Osaka Prefecture, + +Ranunculus japonicus +Thunb. + +, +3.VII.1960 +(coll. M. Sorin) —2 apterous viviparous females; the same locality, host-plant and date (coll. R. Takahashi) —3 apterous viviparous females; the same locality and host-plant, +5.VII.1960 +(coll. M. Sorin) —7 apterous viviparous females; Mt. Iwawaki, Osaka Prefecture, the same host-plant, +30.VII.1960 +(coll. M. Sorin) —3 apterous viviparous females; Hirao, Osaka Prefecture, the same host-plant, +1.XI.1960 +(coll. M. Sorin) —14 gynoparae; the same locality, + +Photinia villosa +(Thunb.) + +DC, +2.XI.1960 +(coll. M. Sorin) —4 oviparous females; the same locality and host-plant, +9.XI.1960 +(coll. M. Sorin) —3 gynoparae; the same locality, + +Ranunculus japonicus +Thunb. + +, +11.XI.1960 +(coll. M. Sorin) —1 gynopara and +7 males +; the same locality, + +Photinia villosa +(Thunb.) + +DC, +11.XI.1960 +(coll. M. Sorin)—1 gynopara and +4 males +; Tanegashima, Kagoshima Prefecture, +2.VI.1973 +(coll. E. Manabe) —4 emigrant or alatae exules. + + + +FIGURES 1–7. + +Miyazakia ranunculi +(Miyazaki, 1971) + +, apterous viviparous female: 1, habitus; 2, front of head; 3, antennae; 4, ultimate segment of rostrum; 5, hind tarsus; 6, siphunculus; 7, cauda. + + + + +Types +. + +Syntypes +of this species + +14 apterous and 4 alate viviparous females – is preserved in the aphid collections of the Laboratory of Systematic Entomology, Department of Ecology and Systematics, Graduate School of Agriculture, Hokkaido University (Kita-ku, Sapporo, +Japan +) [not examined]. + + + + +Description. Alatae viviparous female (emigrant or alate exule) +(4 specements). Body elongated oval or elliptical, 1.9–2.3 (2.1) times as long as its width. Color in life unknown. Cleared specimens with head, thorax, antennae, upper third of the femora, apices of tibia, tarsi, and siphunculi, subgenital and anal plates and cauda dark brown; two last segments of rostrum, femora (except upper thirds) and tibia (except apices) pale brown. Abdominal dorsum with sclerotized bands on all tergites and large marginal maculae on segments I–VII; bands on segments I–II small, thin; sclerotized band and marginal maculae on tergite VII always fused. Head smooth with large, sparse, pointed spinules; dorsal and ventral side of thorax and abdominal tergites I–VI smooth, weakly wrinkled and rarely with large pointed spinules on marginal maculae; tergite VII with short rows of sparse spinules sometimes situated in form of cells, which on tergite VIII become more numerous, partially fused and forming short scales. Two marginal tubercles always present on prothorax and abdominal segments I–V (one of four specimens with one marginal tubercle on segment III). Head without any trace of epicranial coronal suture; frontal tubercles clearly developed, median tubercle not reaching the level of antennal tubercles. Secondary rhinaria are rounded, rarely elliptical, numerous, strongly protruberant, with high cylindrical or slightly conical sclerotized base and with domed projecting membrane, with external diameter 1.3–4.0 times as long as high, spaced evenly along the segment; primary rhinaria with strongly swollen and protruding central membranous part surrounded by long cilia. Rostrum reaching abdominal segment III. Ultimate segment of rostrum narrow, elongate, wedge-shaped. Peritremes on abdominal sternites I and II fused. Siphunculi with 3–7 (4.8) setae, 42-61 (50) µm long. Cauda rounded, escutcheon-like. Two specimens out of four with one pheromone plate on one of the hind tibiae. + + +Apterous viviparous female (exule) +( +15 specimens ++ data of +Miyazaki (1971)) +. Body elliptical or broadly elliptical, 1.6–1.8 (1.6–1.7) times as long as its width. Body in life reddish dark brown dorsally, yellowish brown to dark brown ventrally. Cleared and mounted specimens have brown head, antennae, last two segments of rostrum, legs, bands and marginal maculae on all segments of thorax and abdomen, peritremes, siphunculi, subgenital and anal plate and cauda. Dorsal surface of the thorax and abdomen almost completely sclerotized, bands and marginal maculae on meso- and metathorax and abdominal tergites I–VI fused into a single shield, except for a transparent “window” on the border of tergites V and VI; sclerotized bands and marginal maculae on prothorax and on tergite VII always fused. Surface of frons with sparse, large, pointed spinules, on the rest of head, of dorsal side of thorax, and abdominal tergite IV smooth, slightly wrinkled and only occasionally on marginal maculae and borders of spiracles faintly reticulate (contours of reticulations formed by thin, serrated lines), of tergite VI with sparse large smoothed spinules, which on tergite VII become more numerous and form short rows, and on tergite VIII become pointed and partially fused. Surface of ventral side of abdomen with long rows of small pointed spinules sometimes forming strongly stretched cells. Two marginal tubercles always present on prothorax and abdominal segments I–V (one specimen without marginal tubercles on II); marginal tubercles on abdominal segments I–V protuberant, form hemispherical to conical, sometimes strongly protuberant, smallest tubercles grading to papilliform, diameter of tubercles 1.0–2.8 times as long as high. Two spinal tubercles always present on head, absent elsewhere. Setae on body and appendages pointed or finely pointed. Chaetotaxy of first tarsal segments 3, 3, 2. Head with slight traces of coronary suture, occasionally without. Frontal tubercles not developed, frons flat or very slightly convex. Antennae 6-segmented, without secondary rhinaria; primary rhinaria with ring of long ciliae. Rostrum long, reaching abdominal segments IV–V. Ultimate segment of rostrum elongated, wedge-shaped. Legs normal. Arms of mesosternal furca connected by wide, sclerotized base. Spiracles wide open, roundish reniform. Peritremes on abdominal sternites I and II continuous or fused, or separated by a distance less than diameter of peritreme. Siphunculi cylindrical, narrowing towards apex, with distinct flange, sometimes slightly bottle-shaped (with a wider basal half, gradual narrowing in the middle and an almost cylindrical slightly narrower upper half), with 3–10 (5.0–7.0) setae, 66–91 (75–83) µm long. Siphunculi covered with sparse short rows of pointed spines which are partially fused and form separate scales closer to the apex; sometimes with a row of polygonal cells at apex before flange. Subgenital plate oval. Cauda rounded, escutcheon-like, sometimes slightly wart-shaped due to slight constriction before base. +Hind +tibia with 1–8 (3.7–4.3) rounded pheromone plates at the apex. + + +Alatae viviparous female (gynopara) +( +21 specimens ++ data of +Miyazaki (1971)) +. Body elliptical or elongate egg-shaped, 2.0–2.2 (2.0–2.2) times as long as its width. Body in life blackish brown (M. Sorin, pers. comm.). Two marginal tubercles always present on prothorax and abdominal segments I–V. External diameter of secondary rhinaria 0.8–5.0 times as long as high. Rostrum reaching abdominal segment II. Siphunculi with 3–8 (4.0–7.0) setae, 47–61 (52–59) µm long. 10% of individuals with one circular pheromone plate on one of the hind tibia. + + + +TABLE 1. +Biometric data for emigrants (or alate exules), apterous viviparous female and gynoparae of + +Miyazakia ranunculi +(Miyazaki, 1971) + +. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
MorphsEmigrant or alate exulesApterous Gynopara viviparous female
Number of samples/specimens1/44/15 + data of 5/21 + data of Miyazaki (1971) Miyazaki (1971)
Length of body2032–2107 (2082)1394–2010 1962–2256 (1613–1973) (2009–2177)
Length of antennae1914–2170 (2082)807–1181 1859–2245 (932–1110) (1870–2157)
Length of antennae/length of body0.94–1.03 (1.00)0.50–0.65 0.87–1.08 (0.58) (0.92–1.07)
Hind femora length601–667 (635)415–584 559–704 (470–570) (620–693)
length/length of body0.30–0.32 (0.31)0.25–0.32 0.29–0.33 (0.29) (0.30)
+
+Length of posterior seta on hind trochanter/diameter of trochantro- 1.05–1.14 1.45–2.22 0.91–1.52 +femoral suture (1.08) (1.59–1.90) (0.93–1.35) + +Hind +tibia length +1259–1361 +769–1010 +1165–1426 +(1315) (822–1010) ( +1246–1396 +) on subgenital anterior 7–17 (11.8) 6–16 (9.1–13.3) 4–18 (4.0–13.5) plate posterior 18–25 (22.5) 14–27 (17.6–22.0) 17–28 + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
length/length of body0.62–0.65 (0.63)0.45–0.57 (0.51)0.58–0.68 (0.62)
Tubercles Siphunculus in the middle/ largest tubercle width of the marginal tubercle on abdominal segments I–V smallest tubercle1.46–2.30 (1.87) 2.63–4.30 (3.55)1.50–2.40 (1.82–2.01) 2.22–7.00 (3.44–5.48)1.45–2.75 (1.84–2.34) 3.00–5.50 (3.78–5.50)
number of spinal222
Setae the on 3rd antennal length lon- segment gest length/basal diameter of segment26–49 (33) 1.10–2.33 (1.39)85–115 (96) 4.33–7.00 (4.79–5.89)28–56 (38–46) 1.20–2.22 (1.42–1.86)
on abdo- III length minal tergite length/basal diameter of segment63–73 (67) 2.45–3.44 (2.84)75–122 (90–108) 4.57–6.50 (5.14–5.47)54–85 (66–77) 2.27–3.67 (2.67–3.14)
VIII length63–80 (73)94–129 (109)63–89 (71–84)
length/basal diameter of segment2.70–3.58 (3.05)5.00–8.00 (5.75–6.43)2.67–4.00 (3.06–3.51)
number on 3rd antennal segment12–20 (17.4)14–24 (17.4–21.0)12–26 (18.5–22.5)
accessory on ultimate rostral segment6–7 (6.5)4–6 (4.3–5.7)4–8 (4.0–6.5)
on abdominal tergite VIII6–8 (7.0)6–12 (7.4–10.7)6–11 (7.0–9.0)
+
+ +(17.0–27.0) on cauda 4–5 (4.8) 4–7 (5.2-5.7) 5–7 (5.0–6.3) +......continued on the next page +Morphs Emigrant or Apterous Gynopara + + + +TABLE 1. +(Continued) + + +alate exules viviparous female + + + + + + + + + + + + + + + + + +
Number of secondary rhinaria on 3rd antennal segment48–69 0 (61.4)61–87 (68.0–85.0)
4th18–33 0 (28.7)21–35 (28.7–34.0)
5th17–22 0 (19.4)12–20 (15.0–17.0)
+
+Length of processus terminalis/length of basal part of last antennal 3.94–4.15 2.18–3.06 3.41–5.40 +segment (4.06) (2.54) (4.25–5.05) +Length of 2nd segment of hind tarsus 103–108 93–106 96–108 +(104) (99) (101) +Ultimate Length 167–197 185–216 192–216 +rostral (181) (191–204) (198–207) + +segment length/ length of 2nd segment of hind tarsus 1.61–1.91 1.83–2.18 1.86–2.17 (1.78) (1.90–2.08) (1.90–2.07) +Male +( +15 specimens +). Alate. Body elongated elliptical, 2.2–2.6 (2.2–2.5) times as long as its width. Body in life dark brown (M. Sorin, pers. comm.). Dorsal surface of abdomen with sclerotized bands on all tergites and large marginal maculae on segments I–VII, band on segment II sometimes divided on separate sclerites. Surface of head, dorsal and ventral side of thorax and abdominal tergites I–VI smooth, slightly wrinkled and only sometimes with marginal maculae with sparse, large, pointed spines. Two marginal tubercles always present on prothorax and abdominal segments I–V (one specimen with one marginal tubercle on segment VI). Spinal tubercles present on the head in twelve of fifteen specimens (tubercles paired in nine specimens), absent elsewhere. Rostrum reaching abdominal segment III. Peritremes on abdominal sternites I and II fused and only in one specimen on the one side separated by a distance less than diameter of peritreme. Siphunculi cylindrical, narrowed to apex, with flanges, with 2–5 (3.8) setae, 30–54 (43) µm long. Siphunculi with scales formed from the partially fused pointed spinules. +Hind +tibia without pheromone plates. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
length of siphunculi0.86–0.97 (0.91)0.71–1.13 (0.76–0.95)0.99–1.24 (1.00–1.18)
Siphunculi Length183–218 (197)178–276 (212–252)164–205 (169–202)
length/width of siphunculi at half length3.63–4.63 (4.14)3.30–5.18 (4.22–4.58)3.45–4.53 (3.50–4.17)
Length of cauda6654–70 (58–65)59–76 (63–70)
Length of siphunculi/length of cauda2.89–2.96 (2.93)3.28–4.33 (3.32–4.17)2.37–3.12 (2.43–2.86)
+
+ +Oviparous female +( +6 specimens +). Body broadly elliptical or elliptical, 1.4–1.8 (1.6–1.7) times as long as its width. Body in life dark brown (M. Sorin, pers. comm.). Cleared and mounted specimens with head, antennae, last two segments of rostrum, legs, bands and marginal maculae on all segments of thorax and abdomen, peritremes, siphunculi, subgenital and anal plates, and cauda brown. Dorsal surface of thorax and abdomen with bands and marginal maculae on all segments, bands on some abdominal segments fragmented into rows of partially interconnected, partially free sclerites; sclerotized bands and marginal maculae on tergite VII fused. Surface of head, dorsal side of thorax and abdominal tergites I–V smooth, slightly wrinkled, on tergites VI–VIII with short and rare rows of pointed spinules which on tergite VIII are sometimes fused to form short scales. Marginal and spinal tubercles absent. Chaetotaxy of first tarsal segments 3, 3, 2 and only sometimes one or two fore and middle tarsi with 2 setae. Head with traces of coronary suture. Frontal tubercles are not expressed, frons slightly convex. Antennae 5-segmented, without secondary rhinaria. Rostrum reaching abdominal segment I–II. Ultimate segment of rostrum wedge-shaped. Legs shortened and slightly thickened. Arms of mesosternal furca separated. Peritremes on abdominal sternites I and II separated by a distance lesser than diameter of peritreme. Siphunculi cylindrical, narrowed to apex, with distinct flanges, with 2 long (59–61) setae on each siphunculi. Surface of siphunculi with sparse scales formed from the partially fused spinules. +Hind +tibia swollen in basal half, with 88–93 round pheromone plates located almost the entire length of the tibia, but more of them located in the basal half. + + +Egg +(on + +Photinia + +). Black, shiny, about +0.5 mm +in length (M. Sorin, pers. comm.). + +
+ + +Distribution. +Japan +: Osaka Prefecture, Kagoshima Prefecture (Tanegashima Island); +Korea +( +Blackman and Eastop, 2006 +). + + + + +FIGURES 8–18. + +Miyazakia ranunculi +(Miyazaki, 1971) + +, emigrant (or alatae exules), gynopara, male and oviparous female. 8, abdomen of emigrant (or alate exule); 9, antennae of emigrant (or alate exule); 10, siphunculi of emigrant (or alate exule); 11, siphunculus of gynopara; 12, siphunculus of male; 13, siphunculus of oviparous female; 14, cauda of emigrant (or alate exule); 15, cauda of gynopara; 16, cauda of male; 17, cauda of oviparous female; 18, hind tibia of oviparous female. + + + + +Biology. +Miyazaki described this species from + +Ranunculus japonicus +Thunb. Alate + +viviparous females and alate males from + +Photinia villosa +(Thunb.) + +DC were collected and labeled by Sorin as + +Sappaphis ranunculi + +. Comparison of these specimens with alate females and males collected in the same place and at the same time on + +Ranunculus + +shows that individuals from + +Photinia + +and + +Ranunculus + +do not differ morphologically and therefore the conclusions of Sorin that they belong to the same species were correct. + + + +TABLE 2. +Biometric data for males and oviparous females of + +Miyazakia ranunculi +(Miyazaki, 1971) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
MorphsMales +Oviparous females from + +Photinia + + +Oviparous females from + +Rhamnus + +
Number of samples/specimens3/151/41/2
Length of body1553–1827 (1645–1769)1213–1487 (1345)1218–1340 (1279)
Length of antennae1836–2387 (2062–2279)731–781 (767)711–794 (749)
Length of antennae/length of body1.22–1.31 (1.28)0.52–0.62 (0.57)0.58–0.59
Hind femora length503–601 (529–585)264–308 (290)264–294 (284)
length/length of body0.31–0.36 (0.33)0.20–0.23 (0.22)0.22
Length of posterior seta on hind trochanter/diameter of trochantro-femoral suture0.85–1.24 (1.00)0.96–1.47 (1.23)0.83–0.96 (0.89)
Hind tibia length1035–1221 (1072–1181)492–550 (529)492–518 (506)
length/length of body0.64–0.73 (0.67)0.36–0.42 (0.39)0.38–0.40 (0.39)
Tubercles siphunculus in the middle/ largest tubercle width of the marginal tubercle on abdominal smallest tubercle segments I–V1.25–1.89 (1.44–1.76) 2.58–5.67 (3.51–3.97)- -- -
number of spinal0–2 (0.5–2.0)00
Setae the on 3rd length lon- antennal length/basal diameter of gest segment segment21–38 (32) 0.82–1.56 (1.15–1.35)61–78 (69) 4.17–6.00 (5.00)51–56 (54) 3.14–3.67 (3.32)
on abdo- III length minal length/basal diameter of tergite segment52–63 (58) 2.08–2.75 (2.35)84–91 (87) 5.50–7.55 (6.27)66 3.71–4.33 (4.02)
VIII length54–68 (60)99–106 (104)81–94 (87)
length/basal diameter of segment1.92–3.38 (2.22–2.59)6.83–8.40 (7.48)4.57–6.17 (5.34)
number on 3rd antennal segment20–34 (26.4–27.1)9–12 (10.6)9–11 (10.3)
accessory on ultimate rostral segment5–11 (7.3–8.5)22
on abdominal tergite VIII5–11 (6.8–9.1)19–23 (21.3)18–19 (18.5)
on subgenital anterior plate posterior- -13–29 (18.0) 20–37 (31.3)10–12 (11.0) 30–36 (33.0)
on cauda5–8 (6.5)8–10 (9.0)10–11(10.5)
MorphsMales +Oviparous females from + +Photinia + + +Oviparous females from +Rhamnus +
+
+ +. +.....continued on the next page +Ultimate length 178–202 126–137 116–119 rostral (189) (130) (118) segment length/ length of 2nd segment of hind tarsus 1.80–2.18 1.44–1.54 1.35–1.47 + + + +TABLE 2. +(Continued) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Number of secondary rhinaria on 3rd antennal segment77–109 (92.4–94.9)00
4th23–44 (33.9–37.7)00
5th16–29 (22.7–25.9)00
Length of processus terminalis/length of basal part of last antennal segment4.56–6.32 (5.67–6.12)2.57–3.06 (2.83)2.44–2.61 (2.51)
Length of 2nd segment of hind tarsus89–103 (96)84–92 (88)84–86 (85)
+
+ +(1.95–2.00) (1.48) (1.42) Also among Sorin’s material is an oviparous female collected from + +Photinia + +, similar in a number of morphological characters to the apterous viviparous females from + +Ranunculus + +, allowing it to be identified as this species. Sorin also noted that this female laid eggs on + +Photinia + +(M. Sorin, pers. comm.). It can therefore be concluded with a high degree of confidence that + +Miyazakia ranunculi + +is a heteroecious species that migrates to + +Ranunculus + +from + +Photinia + +, and that alate parthenogenetic females collected in the autumn on + +Ranunculus + +are gynoparae. Plant species belonging to the subfamily +Maloideae +(or subtribe +Pyrinae +in modern classification; +Potter et al., 2007 +) are the most common primary hosts of aphids of subtribe +Anuraphidina +( +Shaposhnikov et al., 1998 +) so that the relationship of the new genus with + +Photinia + +conforms to this trend. However, among Sorin’s slides is one containing two oviparous adults and four larvae of oviparous females collected on + +Rhamnus dahurica +Pall. It + +is known that sometimes oviparous females can develop on an unsuitable host; these oviparae from + +Rhamnus + +are smaller than females from + +Photinia + +(see +Table 2 +) perhaps indicating they were on an unsuitable host. However, it may be a mistake in the determination of plants. On slide no. +11762 in +the collection of Muséum national d'Histoire naturelle, the host-plant was originally specified on the label as " + +Rhamnus dahurica + +", but this had later been crossed out and changed to " + +Pourthiaea villosa + +" (i.e. modern + +Photinia villosa + +). However until a detailed study of the biology of + +Miyazakia ranunculi + +is conducted, + +Rhamnus + +cannot be excluded from the list of possible primary hosts of this species. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
length of siphunculi1.24–1.62 (1.40–1.54)1.00–1.12 (1.07)0.96–1.12 (1.04)
Siphunculi length115–155 (120–138)115–129 (122)106–121 (113)
length/width of siphunculi at half length2.51–3.80 (3.01–3.42)2.25–3.00 (2.47)1.96–2.32 (2.14)
Length of cauda62–68 (65)48–52 (50)-
Length of siphunculi/length of cauda1.74–2.28 (1.94–2.11)2.23–2.68 (2.41)-
+
+ +There is another slide among Sorin’s material containing 4 alate viviparous females collected in yellow pan traps by Mr. E. Manabe on +2 June 1973 +, on the island of Tanegashima (Kagoshima Prefecture). These specimens are morphologically very similar to the gynoparae from + +Ranunculus + +and + +Photinia + +, and Sorin labelled them as + +Sappaphis ranunculi + +. The relatively early date of collection suggests that they may be emigrants, although it is impossible to exclude the possibility that they are alate exules, especially considering that the island of Tanegashima is located in the subtropical zone. + + +Dr. Sorin informed me that the aphids on + +Photinia + +are found on the underside of leaves and those on + +Ranunculus + +are found near the buds (M. Sorin, pers. comm.). + +
+
+
\ No newline at end of file diff --git a/data/38/5A/F8/385AF89C3B2458D8ADEF80A12A11A5EC.xml b/data/38/5A/F8/385AF89C3B2458D8ADEF80A12A11A5EC.xml new file mode 100644 index 00000000000..ab3e72bf1c1 --- /dev/null +++ b/data/38/5A/F8/385AF89C3B2458D8ADEF80A12A11A5EC.xml @@ -0,0 +1,102 @@ + + + +Taxonomic changes in Oenothera sections Gaura and Calylophus (Onagraceae) + + + +Author + +Wagner, Warren L. +Department of Botany, MRC- 166, National Museum of Natural History, Smithsonian Institution, P. O. Box 37012, Washington, DC 20013 - 7012, USA +wagnerw@si.edu + + + +Author + +Krakos, Kyra N. +Biology Department, Maryville University, 650 Maryville University Dr., St. Louis, MO 63141, USA + + + +Author + +Hoch, Peter C. +Missouri Botanical Garden, P. O. Box 299, St. Louis, MO 63166 - 0299, USA + +text + + +PhytoKeys + + +2013 + +2013-11-04 + + +28 + + +61 +72 + + + + +http://dx.doi.org/10.3897/phytokeys.28.6143 + +journal article +http://dx.doi.org/10.3897/phytokeys.28.6143 +1314-2003-28-61 +FFBCE22D163DFF8AFF8EFF954A44FF90 +576178 + + + + +7 +a. +Oenothera capillifolia Scheele subsp. capillifolia + + + + +Oenothera berlandieri +subsp. +pinifolia +(Engelmann) W. L. Wagner & Hoch, Syst. Bot Monogr. 83: 211. 2007. + + + +Basionym. + + +Oenothera serrulata + +var. +pinifolia +Engelmann in A. Gray, Bost. J. Nat. Hist. 6: 189. 1850. + +Meriolix serrulata + +var. +pinifolia +(Engelmann) Small, Bull. Torrey Bot. Club 23: 187. 1896. + +Oenothera serrulata pinifolia + +(Engelmann) Munz, N. Amer. Fl., ser. 2, 5: 141. 1965. + +Calylophus berlandieri pinifolius + +(Engelmann) Towner, Ann. Missouri Bot. Gard. 64: 107. 1977. + + + +Type. +United States. Texas: Comal County, New Braunfels, Apr-May 1846, F. Lindheimer 394 (Holotype: MO-122323!; Isotypes: DS, GH [2]!, K [3]! MO!, NY!, PH, RSA, US!, YU!). + + + \ No newline at end of file diff --git a/data/38/5B/13/385B134D5139328832D3DF2EDB0F5660.xml b/data/38/5B/13/385B134D5139328832D3DF2EDB0F5660.xml new file mode 100644 index 00000000000..27ed121bf9c --- /dev/null +++ b/data/38/5B/13/385B134D5139328832D3DF2EDB0F5660.xml @@ -0,0 +1,169 @@ + + + +Flora der Schweiz und angrenzender Gebiete. Band 2. Nymphaceae bis Primulaceae (2 nd edition) (p. 956): Leguminosae + + + +Author + +Hess, Hans Ernst + + + +Author + +Landolt, Elias + + + +Author + +Hirzel, Rosmarie + +text + +1976 +Birkhaeuser Verlag + + +https://doi.org/10.5281/zenodo.292251 + +book +292251 +10.5281/zenodo.292251 +3-7643-0527-4 + + + +<subSubSection id="3D99C73A981359DD5A5A7A461C2EC4BC" pageId="null" pageNumber="564" type="nomenclature"> +<paragraph id="D0A8F9CE68AAFF7FFF459342B6AC7416" pageId="null" pageNumber="564"> +<taxonomicName id="62A4B71CEA95D67FB80CB3BC451C5269" authority="Retz." class="Magnoliopsida" family="Fabaceae" genus="Astragalus" kingdom="Plantae" order="Fabales" pageId="null" pageNumber="564" phylum="Tracheophyta" rank="species" species="danicus"> +<pageBreakToken id="166719B54D7CA0F9BBAA74FCD050F2E8" pageId="null" pageNumber="564" start="start">Astragalus</pageBreakToken> +<normalizedToken id="58EF090A1A5AAC95886B91B62ABD190C" originalValue="dánicus" pageId="null" pageNumber="564">danicus</normalizedToken> +Retz. +</taxonomicName> +</paragraph> +</subSubSection> +<subSubSection id="BA7B59187301C9AEA9E14B186DC3AB2A" pageId="null" pageNumber="564" type="vernacular_names"> +<paragraph id="5D9EC2EB43EE89ABF00E346C5DD1EDAC" pageId="null" pageNumber="564"> +<normalizedToken id="FAB2451BE5ECCD8452DB84A150886D0D" originalValue="Dänischer" pageId="null" pageNumber="564">Daenischer</normalizedToken> +Tragant +</paragraph> +</subSubSection> + + + +Ausdauernd; 5-30 cm hoch. Stengel niederliegend oder aufsteigend, bis 30 cm lang, verzweigt, zerstreut anliegend behaart bis kahl ( +Haare einfach +). +Blaetter +mit 15-23 +Teilblaettern +; +Teilblaetter +0,5-1,2 cm lang, 2-4mal so lang wie breit, spitz oder ausgerandet, beidseits zerstreut behaart; + +Nebenblaetter +bis +ueber +die Mitte miteinander verwachsen + +, +1/2-11/2 +mal so lang wie die untersten +Teilblaetter +. +Blueten +zu 5-15, aufrecht. Stiel des +Bluetenstandes +11/2 +-2mal so lang wie das +naechststehende +Stengelblatt. + +Tragblaetter +hoechstens + +1/2 + +so lang wie die +Kelchroehre +. + +Kelch 0,6-0,8 cm lang, mit zahlreichen, abstehenden, +weissen +und schwarzen Haaren; +Kelchzaehne +⅖- +1/2 +so lang wie die +Kelchroehre +. +Krone 1,4-1,8 cm lang +, blauviolett, am Grunde +gelblichweiss +. Frucht im Kelch ++/- +ungestielt, aufrecht, +eifoermig +, 0,7-1,2 cm lang und 0,3-0,5 cm dick, an der untern Naht gefurcht, dicht und abstehend +weiss +(seltener auch schwarz) behaart. - +Bluete +: +Spaeter +Fruehling +und +frueher +Sommer. + + + +Zylologische +Angaben. 2n + += +16: +Material unbekannter Herkunft (Tschechow aus Tischler 1950), aus den +Suedwestalpen +(Caussols) (Guinochet und Logeois 1962). + + +Standort. +Kollin, montan und subalpin. Trockene, lockere, meist kalkhaltige, sandige +Boeden +in warmen Lagen. Trockenwiesen, lichte +Waelder +. + + +Verbreitung. Eurasiatische Pflanze: +Westwaerts +vereinzelt bis +Suedwestalpen +, Rhein, Irland; +nordwaerts +bis Schottland, +Suedschweden +, Estland; Kaukasus, Sibirien, Zentralasien; in Nordamerika nahe verwandte Sippen ( + +A. goniatus +Nutt. + +, + +A. striatus +Hooker + +). Verbreitungskarte von Meusel et al. (1965). - Im Gebiet: +Elsass +( +suedoestlich +und nordwestlich von Neuf-Brisach), Savoyen (obere Maurienne), +oestliche +Grajische Alpen (?). + + + + \ No newline at end of file diff --git a/data/38/5B/4F/385B4F3BF230E3440EE75C015EE73BD8.xml b/data/38/5B/4F/385B4F3BF230E3440EE75C015EE73BD8.xml new file mode 100644 index 00000000000..d3d2bcac219 --- /dev/null +++ b/data/38/5B/4F/385B4F3BF230E3440EE75C015EE73BD8.xml @@ -0,0 +1,101 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part L) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +610 +650 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Liquidambar styraciflua +Linnaeus + +, + +Species Plantarum +2 + +: 999. 1753 + + +. + + + +"Habitat in Virginia, Mexico." RCN: 7237. + + + + +Lectotype +(Wijnands, +Bot. Commelins +: 109. 1983): +Kalm +, Herb. Linn. No. 1134.1 ( +LINN +) + +. + + + + +Generitype +of + +Liquidambar +Linnaeus + +(vide Green, +Prop. Brit. Bot. +: 189. 1929). + + + + +Current name: + +Liquidambar styraciflua +L. + +( +Hamamelidaceae +). + + + + \ No newline at end of file diff --git a/data/38/5B/6C/385B6C9F4EAE5549B44BE4C69007E018.xml b/data/38/5B/6C/385B6C9F4EAE5549B44BE4C69007E018.xml new file mode 100644 index 00000000000..1cb1c0d5741 --- /dev/null +++ b/data/38/5B/6C/385B6C9F4EAE5549B44BE4C69007E018.xml @@ -0,0 +1,157 @@ + + + +A maximalist approach to the systematics of a biological control agent: Gryon aetherium Talamas, sp. nov. (Hymenoptera, Scelionidae) + + + +Author + +Talamas, Elijah J. +https://orcid.org/0000-0002-1048-6345 +Florida Department of Agriculture and Consumer Services, Gainesville, FL, USA +elijah.talamas@fdacs.gov + + + +Author + +Bremer, Jonathan S. +Florida Department of Agriculture and Consumer Services, Gainesville, FL, USA + + + +Author + +Moore, Matthew R. +Florida Department of Agriculture and Consumer Services, Gainesville, FL, USA + + + +Author + +Bon, Marie-Claude +https://orcid.org/0000-0001-5914-1682 +USDA-ARS-EBCL, Montpellier, France + + + +Author + +Lahey, Zachary +https://orcid.org/0000-0002-9402-9570 +Department of Evolution, Ecology, and Organismal Biology, The Ohio State University, Columbus, OH, USA + + + +Author + +Roberts, Cheryl G. +Florida Department of Agriculture and Consumer Services, Gainesville, FL, USA + + + +Author + +Combee, Lynn A. +Florida Department of Agriculture and Consumer Services, Gainesville, FL, USA + + + +Author + +McGathey, Natalie +Florida Department of Agriculture and Consumer Services, Gainesville, FL, USA + + + +Author + +van Noort, Simon +https://orcid.org/0000-0001-6930-9741 +Iziko South African Museum, Cape Town, South Africa + + + +Author + +Timokhov, Alexander V. +https://orcid.org/0000-0001-7040-6290 +Lomonosov Moscow State University, Moscow, Russia + + + +Author + +Hougardy, Evelyne +https://orcid.org/0000-0001-7537-470X +USDA-ARS-ISPH, Albany, CA, USA + + + +Author + +Hogg, Brian +USDA-ARS-ISPH, Albany, CA, USA + +text + + +Journal of Hymenoptera Research + + +2021 + +2021-12-23 + + +87 + + +323 +480 + + + + +http://dx.doi.org/10.3897/jhr.87.72842 + +journal article +http://dx.doi.org/10.3897/jhr.87.72842 +1314-2607-87-323 +E343379ED04447ABA1ED47B3F01F3E59 +D03A96052A8550F9918BB08ACA344FB9 +5811493 + + + + +Gryon minimum (Kieffer) + + + + +Hadronotus minimus +Kieffer, 1908: 35 (original description); Kieffer, 1926: 455, 467 (description, keyed). + + +Gryon minimus +(Kieffer): Alayo Dalmau, 1973: 99 (cataloged). + + +Gryon minimum +(Kieffer): Johnson, 1992: 388 (cataloged). + + + +Comments. + +The original description suggests that this species belongs in + +Gryon + +and so we leave it here for now, albeit without great confidence: "head wider than thorax, slightly arched back, twice as wide as long, smooth and shiny on the front which gives an unlimited frontal impression, finely chagrined on the rest." + + + + \ No newline at end of file diff --git a/data/38/5B/87/385B87CBFFE1D07BFF47FF2C31C46936.xml b/data/38/5B/87/385B87CBFFE1D07BFF47FF2C31C46936.xml new file mode 100644 index 00000000000..4ebd534518f --- /dev/null +++ b/data/38/5B/87/385B87CBFFE1D07BFF47FF2C31C46936.xml @@ -0,0 +1,2822 @@ + + + +Taxonomic review of the Andean crab spiders genus Coenypha Simon, 1895 (Thomisidae: Stephanopinae) + + + +Author + +Machado, Miguel + + + +Author + +Previato, Thales + + + +Author + +Grismado, Cristian J. + + + +Author + +Teixeira, Renato + +text + + +Zootaxa + + +2023 + +2023-06-21 + + +5306 + + +3 + + +301 +330 + + + + +http://dx.doi.org/10.11646/zootaxa.5306.3.1 + +journal article +53769 +10.11646/zootaxa.5306.3.1 +0c0b9965-f8a4-4ac8-b84c-f4589d3d79f0 +1175-5326 +8062920 +C1379C64-6C6B-4784-B9E4-6433319EAE3C + + + + + + + +Coenypha ditissima +( +Nicolet, 1849 +) + + + + + + + +Figs 6A–F +, +7A–F +, +14B + + + + + + + +Thomisus ditissimus +Nicolet, 1849: 394 + + +, pl. 3, fig. 9. +Holotype +female from Valdivia, +Chile +, deposited in MNHN (4176), examined. + +Ramírez 1989: 11 + +. + + + + + + +Thomisus spissus +Nicolet, 1849: 395 + + +. +Holotype +female from +Chile +, deposited in MNHN (4178), examined. + +Ramírez 1989: 11 + +. +New Synonymy. + + + + + + +Thomisus variabilis +Nicolet, 1849: 396 + + +. +Holotype +male (together +two immatures +) from +Chile +, deposited in MNHN (4180), examined. +Roewer 1955 +(declared +nomen dubium +, rejected here); + +Ramírez 1989: 11 + +. +New Synonymy. + + + + + +Stephanopis ditissima +(Nicolet) + +: + +Keyserling 1880: 175 + +, pl. 3, fig. 96; +Simon 1887 +: E8, pl. 2, fig. 1; Mello-Leit„o 1951: 332, fig. 7; + +Ramírez 2014: 223 + +, figs 151E–F, 172E; + + +Machado +et al. +2017: 454 + + +, fig. S12C; + +Machado and Teixeira 2021: 296 + +(transferred to + +Coenypha + +). + + + + + +Stephanopis spissa +(Nicolet) + +: + +Simon 1895: 1054 + +. + + + + +Stephanopis maulliniana +Mello-Leit + +„o, 1951: 334. +Holotype +female from +Maullín +, +Llanquihue +, +Chile +, deposited in MNRJ, examined. +New Synonymy. + + + + + +Misumenoides nicoleti +Roewer, 1951: 448 + + +. Replacement name for + +Thomisus cinereus +Nicolet, 1849 + +due to homonymy with + +Thomisus cinereus +C. L. +Koch, 1837 + +. Synonymized by + +Lehtinen & Marusik (2008: 186) + +with + +Misumenops temibilis +( +Holmberg, 1876 +) + +, here rejected. +New Synonymy. + + + + + +Note: +In the case of + +T. ditissimus + +, there was a single spider in the vial MNHN 4176, therefore we can consider this specimen the type by monotypy as stated in article 73.1.2 of the +ICZN (2022) +.Two species described by Nicolet in 1849 ( + +T. cinereus + +and + +T. variabilis + +) have been part of a confusing taxonomic history that involved several species of the distantly related genera + +Misumenoides +F. O. +Pickard-Cambridge, 1900 + +and + +Misumenops +F. O. +Pickard-Cambridge, 1900 + +, originated from taxonomic decisions made without the examination of the type specimens (see Mello-Leit„o 1939; +Roewer 1955 +and especially, the discussion of +Lehtinen & Marusik 2008 +). As a result of this, the Stephanopine + +Thomisus cinereus +Nicolet, 1849 + +appeared listed among the synonyms of + +Misumenops temibilis +( +Holmberg, 1876 +) + +, a species belonging in the tribe +Misumenini +. Although the type specimens of these species have been found (the vial MNHN 4182 is + +T. cinereus +Nicolet, 1849 + +, and MNHN 4180 is + +T. variabilis + +), as reported by +Ramírez (1989) +, those were unfortunately overlooked by +Lehtinen and Marusik (2008) +. Considering the abovementioned and according to article 75.8 of the +ICZN (2022) +, we do not recognize the +neotype +of + +T. cinereus + +(= + +T. nicoleti + +) proposed by +Lehtinen & Marusik (2008) +and therefore, their synonymy with + +Misumenoides temibilis + +. Moreover, we examined all Nicolet’s types listed above in synonymy of + +Coenypha ditissima + +and conclude that there are no significant differences between them, hence they should be considered synonyms. Finally, the priority of + +T. ditissimus + +over + +T. cinereus + +(= + +T. nicoleti + +), + +T. spissus + +, and + +T. variabilis + +(ICZN 2.4.2.1 and 2.4.2.2.) is given once +Nicolet (1849) +mention this species prior the other three in the literature. + + + + +Other material examined. + + +ARGENTINA +: + +Neuquén + +: + +1♁ and + + +1♀ +, +Lanín +, +40°6’19.00”S +, +71°40’11.00”W +, + +January 1985 + +, +M. Ramírez +( +MACN-Ar 18651 +) + +; + +1j, +Lago Lácar +, +40°10’37.79”S +, +71°29’38.80”W +, + +January 1954 + +, +N. Kormilev +( +MACN-Ar 4164 +) + +; + +1j, +Parque Nacional Nahuel Huapi +, +40°53’27.87”S +, +71°34’34.11”W +, + +30 January 1985 + +, +M. Ramírez +( +MACN-Ar 18663 +) + +; + +1♁, +Nahuel Huapi +, +40°55’36.13”S +, +71°29’34.65”W +, 1945, +D. Hiebermann +( +MACN-Ar 18669 +) + +; + +1♀ +, +Nahuel Huapi +( +Puerto Blest +), +41°1’59.98”S +, +71°49’0.05”W +, + +07–20 January 2000 + +, +L. Lopardo +& +A. Quaglino +( +MACN-Ar 18650 +) + +. + + +Río Negro +: + +2j, +Bariloche +, +41°8’44.93”S +, +71°17’56.85”W +, + +February 1954 + +, M.E. +Galliano +( +MACN-Ar 5404 +) + +. + + + +Chubut + +: + +1♀ +, +Lago Puelo +, +42°5’49.20”S +, +71°36’44.20”W +, + +10–11 December 2021 + +, M. +Pacheco +, L. +Piacentini +& E. +Soto +( +MACN-Ar 42752 +) + +; + +1♀ +, same locality, date and collectors of the previous vial ( +MACN-Ar 42751 +) + +; + +1j, +Parque Nacional Los Alerces +, +42°58’26.85”S +, +71°38’37.90”W +, + +February 1985 + +, +M. Ramírez +( +MACN-Ar 18657 +) + +. + + + +Tierra del Fuego + +: + +1♀ +, +Isla +de losEstados, +54°47’59.46”S +, +64°25’36.47”W +, + +April 1935 + +, J.B. +Daguerre-Cancelles +( +MACN-Ar 18652 +) + +; + +2♀ +and 7j, +Ushuaia +, +54°48’19.44”S +, +68°19’27.14”W +, + +16 February 1949 + +, +B. Aguirre +( +MACN-Ar 2796 +) + +; + +1♀ +, same locality of the previous vial, + +23 January 1960 + +, A. +Bachmann +( +MACN-Ar 18658 +) + +; + +1♀ +, +Parque Nacional +Tierra del Fuego +, margen E del +Lago Roca +, +15 km +W deUshuaia, +54°49’32.92”S +, +68°33’46.80”W +, + +04 December 2012 + +, M. +Ramírez +, C. +Grismado +, +A. Ojanguren +& +E.M. Soto +( +MACN 29783 +) + +; + +1j, same locality of the previous vial, + +February 1963 + +, +Maury +( +MACN-Ar 18666 +) + +. + + +CHILE +: + +Coquimbo + +: + +3j, +Choapa +, +31°48’14.70”S +, +71°0’8.03”W +, + +13 November 1987 + +, +Maurj +( +MACN-Ar 18668 +) + +. + + + +Valparaíso + +: + +1♀ +and 2j, +Zapallar +, +32°33’13.70”S +, +71°27’29.29”W +, 27 +November +, +Ross +& +Michelbacher +( +CAS 9071265 +) + +; + +2♁ and 2j, same locality, date and collectors of the previous vial ( +CAS 9071264 +) + +; + +2j, +Quintero +, +32°46’20.32”S +, +71°31’59.88”W +, + +12 December 1980 + +, +L. Peña +( +AMNH +) + +; + +1♀ +, +Caracoles +, +32°47’30.18”S +, +70° 3’38.57”W +, + +August 1943 + +, +Rosa +( +CAS 9072308 +) + +; + +1♀ +, +Quillota +( +Parque Nacional La Campana +), +32°57’40.40”S +, +71° 3’34.00”W +, + +18 February 2005 + +, M. +Ramírez +& F. +Labarque +( +MACN-Ar 10848 +) + +; + +6j, +El Melón +, +33° 3’55.11”S +, +71°35’25.08”W +, + +03 November 1981 + +, +L. Peña +( +AMNH +) + +; + +1j, +Tunquén +, +33°16’25.45”S +, +71°38’49.10”W +, + +14 October 1982 + +, +M. Pino +( +MHNS 630 +) + +. + + + +Santiago + +: + +6♀ +and 4j, +Quilicura +, +33°21’27.63”S +, +70°43’45.38”W +, + +May 1979 + +, L. +Peña +( +AMNH +) + +; + +1♀ +, +Las Condes +, +33°23’56.33”S +, +70°33’26.32”W +, + +January 1983 + +, no collector given ( +MHNS 739 +) + +; + +5♀ +and 3j, +Cordoba Coast +, +33°26’56.00”S +, +70°40’9.35”W +, + +15–20 February 1979 + +, +L. Peña +( +AMNH +) + +; + +1♀ +, +Malleco +, +33°30’37.01”S +, +70°40’16.68”W +, + +November 1979 + +, +L. Peña +( +AMNH +) + +; + +15j, +Cuesta La Dormida +, +33°31’16.74”S +, +70°47’42.40”W +, + +13–18 November 1982 + +, L. +Peña +( +AMNH +) + +; + +2♀ +,15j, +El Canelo +, +33°34’34.36”S +, +70°27’0.00”W +, 1980, +L. Peña +( +AMNH +) + +; + +1♀ +, +Guayacán +, +33°35’60.00”S +, +70°22’0.12”W +, + +January 1984 + +, +P. Goloboff +( +MACN-Ar 18704 +) + +; + +1♀ +, +Pirque +, +33°40’45.64”S +, +70°34’59.19”W +, + +05 October 1982 + +, +L. Peña +( +AMNH +) + +; + +1♀ +and 1j, +Rio Maipo Región +, +33°42’6.78”S +, +70°20’8.44”W +, + +November 1984 + +, G. +Arriagada +( +MHNS 892 +) + +; + +3♀ +, +Melipilla +( +La Viluma +), +33°46’54.04”S +, +71°4’44.55”W +, + +14 May 1980 + +, +L. Peña +( +AMNH +) + +. + + + +Maule + +: + +1♁, +Talca (Provincia de Linares) +, +35°50’47.07”S +, +71°35’58.61”W +, + +11–20 November 1964 + +, L. +Peña +( +MCZ +) + +. + + + +Bío-Bío + +: + +1♁, +Ñuble +( +Las Trancas +), +36°37’9.12”S +, +72° 4’55.24”W +, + +17 February 1983 + +, +L. Peña +( +AMNH +) + +; + +1♀ +, +Ñuble +( +Fundo Los Robles +), +36°42’16.20”S +, +71°36’9.60”W +, + +15 February 2005 + +, +M. Ramírez +& +F. Labarque +( +MACN-Ar 10847 +) + +; + +1♀ +, +Concepción +( +Chome +), +36°42’52.73”S +, +73° 8’21.39”W +, + +07 December 1995 + +, +T. Cekalovic +( +AMNH +) + +; + +1♀ +and 1j, 50 +Km +east of +San Carlos +, +36°43’21.27”S +, +71°45’44.09”W +, + +26 December 1950 + +, +Ross +& +Michelbacher +( +CAS 9072307 +) + +; + +1j, +Concepción +( +Bosque Ramuntcho +), +36°45’10.41”S +, +73°11’8.79”W +, + +14–16 October 1961 + +, +A.F. Archer +( +AMNH +) + +; + +1♀ +, +Concepción +( +Hualpén +), +36°47’12.03”S +, +73°6’35.83”W +, + +11 January 1989 + +, +M. Ramírez +( +MACN-Ar 18655 +) + +; + +2♁, +Concepción +( +Periquillo +), +36°49’12.49”S +, +73°2’39.80”W +, + +21 December 1996 + +, +T. Cekalovic +( +AMNH +) + +; + +1♀ +and 1♁, same locality and collector of the previous vial, + +16 March 1997 + +( +AMNH +) + +; + +1♀ +, same locality and collector of the previous vial, + +20 January 1996 + +( +AMNH +) + +; + +1♀ +, same locality and collector of the previous vial, + +22 March 1997 + +( +AMNH +) + +; + +4♁ and 2j, same locality and collector of the previous vial, + +29 December 1996 + +( +AMNH +) + + +2j, +Camino Chome Ramuntcho +, +36°49’8.18”S +, +73°3’1.15”W +, + +08 November 1996 + +, +T. Cekalovic +( +AMNH +) + +; + +1♀ +, +Ñuble +( +Las Comadres +), +36°53’14.22”S +, +71°34’12.75”W +, + +05–09 February 1983 + +, +L. Peña +( +AMNH +) + +; + +1j, +El Manzano +, +36°54’58.31”S +, +72°54’49.50”W +, + +23 December 1996 + +, +T. Cekalovic +( +AMNH +) + +; + +1♀ +, +El Abanico +, +37°20’27.52”S +, +71°31’57.53”W +, + +30 December 1950 + +, +Ross +& +Michelbacher +( +CAS 9072309 +) + +; + +1♁ and 1j, +Ancon +, +37°48’21.86”S +, +72°42’13.70”W +, + +28 November 1950 + +, +E. Zapudo +( +CAS 9071267 +) + +. + + + +Araucanía + +: + +1♀ +, +Parque Nacional Nahuelbuta +, +37°49’24.60”S +, +72°58’57.00”W +, + +07–25 December 2002 + +, M. +Thayer +& A. +Newton +( +FMNH 2857856 +) + +; + +2j, +Parquenco +, +38°9’48.82”S +, +72°31’13.74”W +, + +06 January 1951 + +, +Ross +& +Michelbacher +( +CAS 9071271 +) + +; + +11j, +Malalcahuello +, +38°28’19.37”S +, +71°36’21.67”W +, + +13–31 December 1982 + +, +A. Newton +& +M. Thayer +( +AMNH +) + +; 9♁, + +9♀ +and 6j, +Cautín +( +Chacamo +), +38°34’56.21”S +, +73°3’11.75”W +, + +17–23 February 1981 + +, +L. Peña +( +AMNH +) + +; + +1♁, +Cautín +( +Temuco +), +38°44’9.25”S +, +72°35’25.35”W +, + +January 1989 + +, +M. Ramírez +( +MACN-Ar 18656 +) + +; + +1♀ +, +Villarica +, +39°16’55.24”S +, +72°13’50.81”W +, + +03 March 1965 + +, +H. Levi +( +MCZ 133890 +) + +; 2♁, + +1♀ +and 1j, same locality, date and collector of the previous vial ( +MCZ 133891 +) + +; + +1♀ +, +Northeast of Villarica +, +39°16’55.25”S +, +72°13’50.81”W +, + +16-31 December 1964 + +, L. +Peña +( +MCZ +) + +. + + +Los Ríos + +: + +2♁ and + +3♀ +, +Valdivia +( +Sender Los Tapuales +as +Renoval Canelos +), +39°49’10.51”S +, +73°14’42.76”W +, + +09January2002 + +, +T.Cekalovic +( +FMNH71617 +) + +; + +4♁and3j, +Las Lajas +, +39°49’10.51”S +, +73°14’42.76”W +, + +09–13 January 1990 + +, +L. Peña +( +AMNH +) + +; + +1♀ +and 1j, +Valdivia +, +39°49’6.53”S +, +73°14’37.94”W +, + +13 January 1951 + +, +Ross +& +Michelbacher +( +CAS 9071266 +) + +; + +4♀ +and 11j, same locality of the previous vial, + +December 1982 + +, E. +Krahmer +( +MHNS 695 +) + +; 1♁, + +3♀ +and 3j, same locality and collector of the previous vial, 1984 ( +MHNS 841 +) + +; 1♁, + +11♀ +and 1j, same locality and collector of the previous vial, 1983 ( +MHNS 804 +) + +; 1♁ and + +1♀ +, +Corral +, +39°53’18.87”S +, +73°25’53.76”W +, + +16 January 1989 + +, +M. Ramírez +( +MACN-Ar 18654 +) + +. + + + +Los Lagos + +: + +1♀ +, +Osorno +( +Pucatrihue +), +40°32’6.87”S +, +73°42’31.82”W +, + +February 1967 + +, +L. Peña +( +MCZ 133410 +) + +; + +1♀ +, same locality and collector of the previous vial, + +25–31 January 1978 + +( +AMNH +) + +; 3♁, + +1♀ +and 9j, +Osorno +( +Puyehue +), +40°34’34.28”S +, +73°6’53.81”W +, + +24 January 1951 + +, +Ross +& +Michelbacher +( +CAS 9072306 +) + +; 3♁, + +3♀ +and 4j, same locality and collector of the previous vial, + +25 January 1951 + +( +CAS 9071270 +) + +; + +2♀ +and 2j, +Osorno +( +La Picada +), +40°34’48.75”S +, +73°10’34.90”W +, + +15-20 January 1980 + +, +L. Peña +( +AMNH +) + +; 1♁ and + +1♀ +, +Osorno +( +Petrohue +), +40°34’52.18”S +, +73°9’19.58”W +, + +13 January 1980 + +L. Peña +( +AMNH +) + +; 1♁, + +2♀ +and 2j, +Osorno +( +Salto Pilmaiquén +), +40°39’11.36”S +, +72°39’36.24”W +, + +26 January 1951 + +, +Ross +& +Michelbacher +( +CAS 9071268 +) + +; + +1j, +Osorno +( +Anticura +), +40°39’12.71”S +, +72°15’44.90”W +, + +November 1982 + +, no collector ( +MHNS 709 +) + +; + +6j, +Aguas Calientes +( +Parque Nacional Puyehue +), +40°43’16.56”S +, +72°19’3.87”W +, + +19-26 December 1982 + +, +A. Newton +& +M. Thayer +( +AMNH +) + +; + +4j, +Aguas Calientes +( +Parque Nacional Puyehue +), +40°43’43.88”S +, +72°18’43.16”W +, + +13–17 December 1998 + +, +M. Ramírez +, +L. Compagnucci +, C. +Grismado +& L. +Lopardo +( +MACN-Ar 18662 +) + +; + +1♀ +, +Aguas Calientes +( +Parque Nacional Puyehue +), +40°43’43.88”S +, +72°18’43.17”W +, + +02–05 January 1982 + +, +L. Peña +( +AMNH +) + +; + +1♀ +, +Llanquihue +( +Entre Lagos +), +40°58’36.61”S +, +72°52’55.06”W +, + +20 January 1969 + +, +L. Peña +( +MCZ 133667 +) + +; + +1♀ +, +Llanquihue +( +Ensenada +), +41°12’25.50”S +, +72°32’19.60”W +, + +18 March 1965 + +, +H. Levi +( +MCZ 133893 +) + +; + +1♁, +Llanquihue +( +Correntoso +), +41°15’38.27”S +, +73°0’28.23”W +, + +January 1969 + +L. Peña +( +MCZ +) + +; 1♁, + +1♀ +and 3j, +Puerto Varas +, +41°19’0.12”S +, +72°58’59.88”W +, + +16 January 1951 + +, +Ross +& +Michelbacher +( +CAS 9072305 +) + +; + +1♁, +Llanquihue +( +Chamisa +), +41°21’38.30”S +, +72°31’13.74”W +, + +13 December 1968 + +, +L. Peña +( +MCZ 133413 +) + +; 2♁, + +3♀ +and 6j, +Llanquihue +( +Los Muermos +), +41°23’57.87”S +, +73°27’53.96”W +, + +19 January 1951 + +, +E.I. Schlinger +& +E.S. Ross +( +CAS 9071269 +) + +; 5♁, + +13♀ +and 10j, same locality and date of the previous vial, +Ross +& +Michelbacher +( +CAS 9071272–9071273 +) + +; + +3♁ and 1j, +Llanquihue +( +Correntoso +), +41°25’13.82”S +, +72°40’11.31”W +, + +December 1968 + +, +L. Peña +( +MCZ 133407 +) + +; + +1♁ and 2j, same locality ad collector of the previous vial, + +20–25 January 1980 + +( +AMNH +) + +; + +1♁, +Llanquihue +( +Puerto Montt +), +41°28’8.10”S +, +72°56’28.09”W +, + +February 1983 + +, +G. Arriagada +( +MHNS 715 +) + +; + +1♁, +Llanquihue +( +X Región +), +41°34’59.99”S +, +72°40’60.00”W +, + +13–15 January 1990 + +, +L. Peña +( +AMNH +) + +; + +1♁, +Lepihué +, +41°35’17.85”S +, +73°33’52.64”W +, + +21 January 1951 + +, +Ross +& +Michelbacher +( +CAS 9071263 +) + +; 1♁ and + +1♀ +, +Isla Grande de Chiloé +( +Guabún +), +41°49’34.75”S +, +74° 1’57.21”W +, + +13–15 January 1980 + +, L. +Peña +( +AMNH +) + +; + +1♀ +, +Isla Grande do Chiloé +(Puente +Rio Pudeto +), +41°52’40.12”S +, +73°50’9.60”W +, + +17 February 1996 + +, T. +Cekalovic +( +AMNH +) + +; + +1♀ +, +Isla Grande de Chiloé +( +Duhatao +), +41°58’50.74”S +, +74° 2’25.97”W +, + +16–21 January 1981 + +, L. +Peña +( +AMNH +) + +; + +1♁, +Puntra +, +42°7’7.39”S +, +73°48’39.88”W +, + +21–23 December 1981 + +, +L. Peña +( +AMNH +) + +; + +1♁, +Isla Grande de Chiloé +( +Butalcura +), +42°13’59.88”S +, +73°44’60.00”W +, + +21 February 1997 + +, T. +Cekalovic +( +AMNH +) + +; 14♁, + +15♀ +and 10j, +Isla Grande de Chiloé +( +Dalcahue +), +42°22’29.25”S +, +73°39’6.35”W +, + +01 February 1981 + +, L. +Peña +( +AMNH +) + +; + +2♀ +, +Isla Grande de Chiloé +( +Dalcahue +), +42°22’39.47”S +, +73°39’6.78”W +, same collector of the previous vial, + +01–04 April 1941 + +( +MCZ 133412 +) + +; + +1♀ +, +Isla Grande de Chiloé +( +Cole Cole +), +42°25’22.39”S +, +74°4’58.62”W +, + +08–11 February 1991 + +, M. +Ramírez +( +MACN-Ar 18648 +) + +; + +2♀ +and 3j, +Isla Grande de Chiloé +( +Gicao +), +42°27’22.52”S +, +73°52’47.37”W +, + +February 1981 + +, L. +Peña +( +AMNH +) + +; + +1♀ +and 1j, +Isla Grande de Chiloé +( +Cerros de Cucao +), +42°28’60.00”S +, +74°3’46.00”W +, + +01 March 1981 + +, L. +Peña +( +AMNH +) + +; + +2♀ +, +Isla Quinchao +( +Hullar Alto +), +42°28’9.00”S +, +73°30’53.00”W +, + +15 January 2002 + +, +T. Cekalovic +( +FMNH 71620 +) + +; 4♁, + +3♀ +and 1j, same locality and collector of the previous vial, + +19 February 1997 + +( +AMNH +) + +; + +2♀ +, same locality and collector of the previous vial, + +16 February 1996 + +( +AMNH +) + +; + +2♁, +Isla Grande de Chiloé +( +Chepu +), +42°31’24.34”S +, +73°52’47.36”W +, + +30 January 1981 + +, L. +Peña +( +AMNH +) + +; + +1♀ +and 1j, +Isla Grande de Chiloé +( +Puente La Caldera +), +42°37’26.28”S +, +73°55’35.66”W +, + +18 February 1997 + +, T. +Cekalovic +( +AMNH +) + +; + +2♀ +, same locality and collector of the previous vial, + +15 February 1996 + +( +AMNH +) + +; 1♁ and + +1♀ +, +Isla Grande de Chiloé +, +42°37’26.29”S +, +73°55’35.66”W +, + +04 February 2001 + +, T. +Cekalovic +( +FMNH 71619 +) + +, + +1♀ +, + +10 January 2002 + +( +FMNH 71630 +) + +; + +11♀ +, + +19 February 1996 + +( +AMNH +) + +, 1♁ and + +2♀ +, + +14 February 1996 + +( +AMNH +) + +, 2♁ and + +4♀ +, + +17 February 1997 + +( +AMNH +) + +, + +1♀ +, + +19 February 1997 + +( +AMNH +) + +, 1♁ and + +1♀ +, + +22 February 1997 + +( +AMNH +) + +, + +2♀ +, + +15-19 March 1981 + +, L. +Peña +( +AMNH +) + +, + +1♀ +and 2j, + +22 February 1997 + +, T. +Cekalovic +( +AMNH +) + +; + +1♁, +Isla Grande de Chiloé +( +Piruquihue +), +42°37’26.29”S +, +73°55’35.65”W +, + +10 February 1993 + +, T. +Cekalovic +( +AMNH +) + +; + +1♀ +, +Isla Grande de Chiloé +( +Cucao +), +42°37’59.88”S +, +74°7’0.12”W +, + +01 February 1991 + +, M. +Ramírez +( +MACN-Ar 18649 +) + +; + +1♀ +and 1j, +Isla Lemuy +( +Puerto Haro +), +42°37’9.00”S +, +73°38’57.00”W +, + +20February1996 + +, +T.Cekalovic +( +AMNH +) + +; + +1♀ +, +Isla Grande de Chiloé +( +Puente Trainel +), +42°40’30.57”S +, +73°47’57.64”W +, + +18 February 1997 + +, T. +Cekalovic +( +AMNH +) + +; + +3♁ and 3j, +Isla Grande de Chiloé +( +Terao +), +42°42’40.07”S +, +73°39’16.15”W +, + +18–21 February 1990 + +, L. +Peña +( +AMNH +) + +; + +4♀ +, +Isla Grande de Chiloé +( +San Antonio de Chadmo +), +42°54’15.73”S +, +73°38’17.02”W +, + +08 February 2001 + +, T. +Cekalovic +( +FMNH 61793 +) + +; + +2j, +Palena +( +Chaitén +), +42°54’41.51”S +, +72°42’56.30”W +, + +04 December 1981 + +, +N. Platnick +& +R.T. Schuh +( +AMNH +) + +. + + + +Aysén + +: + +2♀ +, +46°23’54.41”S +, +72° 0’1.76”W +, + +17 February 1991 + +, M. +Ramírez +( +MACN-Ar 18647 +) + +; + +2♀ +and 10j, +Aisén del General Carlos Ibanez del Campo +, +46°24’43.55”S +, +72°14’33.98”W +, + +27 January 1990 + +, L. +Peña +( +AMNH +) + +; + +1♀ +, +Parque Nacional Los Glaciares +, +50°19’50.00”S +, +73°14’3.00”W +, + +17 January 1972 + +, +E. Hernandez +( +MACN-Ar 18665 +) + +; + +2♀ +, +Magallanes +( +Puerto Natales +, +Torres del Paine +), +51°43’40.76”S +, +72°30’5.84”W +, + +12 December 2009 + +, +L. Almeida +, +H. Wood +& C. +Griswold +( +IBSP 155000 +) + +. + + + + +Diagnosis. +Females of + +C. ditissima + +resemble those of + +C. foliacea + + +sp. nov. + +by the short prosoma covered by hyaline setae ( +Fig. 6B +) and opisthosoma posteriorly enlarged, bearing two pairs of blunt and short projections disposed dorsolaterally, almost like dorsal bumps on the opisthosoma ( +Fig. 6A +) (discrete and flattened in + +C. foliacea + + +sp. nov. + +, +Fig. 10A +). Moreover, + +C. ditissima + +can be distinguished from + +C. foliacea + + +sp. nov. + +by the presence of stout femoral apophysis on legs I and II (like in + +C. edwardsi + +), epigynal plate with anteriorly narrow MSept and long copulatory duct ( +Figs 6C, 6D +) coiling on itself before reaching the spermatecha ( +Figs 6C, D, E, F +) (instead of going straight except for a short anterior curve in + +C. foliacea + + +sp. nov. + +, +Figs 10C, D, E, F +). Males can be distinguished from its congeneric species by the presence of a guanine white-spot on the thoracic portion of prosoma ( +Fig. 7A +) and by the palp presenting a long ribbon-shaped embolus that rests coiled on the tegular ridge instead of encircling the tegulum ( +Fig. 7C +). + + + + +FIGURE 6. + +Coenypha ditissima +( +Nicolet, 1849 +) + +, female (AMNH). A–B habitus (A dorsal, B frontal); C, E epigyne ventral; D, F vulva dorsal. + + + + +FIGURE 7. + +Coenypha ditissima +( +Nicolet, 1849 +) + +, male (FMNH 71619). A–B habitus (A dorsal, B frontal); C–F left palp (C, E ventral, D, F retrolateral). + + + + + +Description. +Female +(from +Los Lagos +,AMNH): + +Anterior eye row recurved and posterior row slightly recurved; ALE have almost twice the diameter of the AME ( +Figs 6A, B +). Prosoma reddish-brown on the cephalic portion and yellowish-brown on the thoracic area, being entirely covered by needle-shaped and filiform setae ( +Figs 6A, B +). Legs I and II predominantly yellowish-brown, with darker patellae; legs III and IV predominantly reddish-brown with metatarsi, tarsi and the proximal portion of the femora lighter. Opisthosoma with an accentuated concavity on the anterior margin, yellowish-brown on the dorsum and median-posterior area; reddish-brown on the sides and projections ( +Fig. 6A +). Copulatory openings are long and narrowed ( +Figs 6C, E +), leading to long and membranous copulatory ducts; spermathecae black, walnut-shaped and sclerotized ( +Fig. 6D, F +). Measurements: eyes diameters and eyes interdistances: AME 0.09, ALE 0.15, PME 0.15, PLE 0.17, AME-AME 0.19, AME-ALE 0.09, PME-PME 0.17, PME-PLE 0.15. MOQ length 0.41, MOQ posterior width 0.51, MOQ anterior width 0.38; leg formula: 1243: leg I—femur 2.52/ patella 1.23/ tibia 1.69/ metatarsus 1.56/ tarsus 0.93/ total 7.93; II—2.28/ 1.06/ 1.47/ 1.29/ 0.80/ 6.90; III—1.28/ 0.81/ 0.79/ 0.63/ 0.52/ 4.03; IV—1.72/ 0.80/ 1.11/ 0.75/ 0.55/ 4.93. Prosoma length 2.50, width 2.62, opisthosoma length 3.56, total body length 6.06; clypeus height 0.35, sternum length 1.27, width 1.14, endites length 0.68, width 0.34, labium length 0.39, width 0.46. + + + +Male +(FMNH 71619): + +Eyes as in the female.Prosoma reddish-brown,lighter in the median portion and presenting a triangular guanine spot on the thoracic area ( +Fig. 7A +). Anterior legs (I and II) light-brown and posterior (III and IV) predominantly yellow, darker on patellae. Cymbium presents a retrolateral concavity/arching to accommodate the embolus ( +Figs 7D, F +). Tegulum discoid, rough-surfaced ( +Figs 7C, E +); RTA short and acute. Measurements: eye diameters and interdistances: AME 0.08, ALE 0.12, PME 0.13, PLE 0.11, AME-AME 0.14, AME-ALE 0.09, PME-PME 0.16, PME-PLE 0.15. MOQ length 0.32, MOQ posterior width 0.41, MOQ anterior width 0.30; leg formula: 1243: leg I—femur 2.36/ patella 0.94/ tibia 1.86/ metatarsus 1.64/ tarsus 1.01/ total 7.81; II—1.96/ 0.80/ 1.40/ 1.27/ 0.78/ 6.21; III—1.02/ 0.57/ 0.70/ 0.55/ 0.46/ 3.30; IV—1.28/ 0.56/ 0.90/ 0.74/ 0.49/ 3.97. Prosoma length 2.07, width 1.90, opisthosoma length 2.02, total body length 4.09; clypeus height 0.30, sternum length 0.89, width 0.95, endites length 0.51, width 0.27, labium length 0.30, width 0.37. + + + + +Distribution. +ARGENTINA +: +Neuquén +, +Río Negro +, +Chubut +and +Tierra del Fuego +; +CHILE +: +Coquimbo +, +Valparaíso +, +Santiago +, +Maule +, +Bío-Bío +, +Araucanía +, +Los Ríos +, +Los Lagos +and +Aysén +( +Fig. 14B +). + + + + \ No newline at end of file diff --git a/data/38/5B/87/385B87CBFFE2D063FF47FF2C316B6AF4.xml b/data/38/5B/87/385B87CBFFE2D063FF47FF2C316B6AF4.xml new file mode 100644 index 00000000000..f3dd9e6b5cf --- /dev/null +++ b/data/38/5B/87/385B87CBFFE2D063FF47FF2C316B6AF4.xml @@ -0,0 +1,519 @@ + + + +Taxonomic review of the Andean crab spiders genus Coenypha Simon, 1895 (Thomisidae: Stephanopinae) + + + +Author + +Machado, Miguel + + + +Author + +Previato, Thales + + + +Author + +Grismado, Cristian J. + + + +Author + +Teixeira, Renato + +text + + +Zootaxa + + +2023 + +2023-06-21 + + +5306 + + +3 + + +301 +330 + + + + +http://dx.doi.org/10.11646/zootaxa.5306.3.1 + +journal article +53769 +10.11646/zootaxa.5306.3.1 +0c0b9965-f8a4-4ac8-b84c-f4589d3d79f0 +1175-5326 +8062920 +C1379C64-6C6B-4784-B9E4-6433319EAE3C + + + + + + + +Coenypha antennata +( +Tullgren, 1902 +) + + + + + + + +Figs 4A–F +, +5A–F +, +14A + + + + + + + +Stephanopis antennata +Tullgren, 1902: 52 + + +, pl. 5, fig. 4. +Holotype +female from +Aysén +, +Chile +(deposited in the NHRS, examined). + +Machado and Teixeira 2021: 296 + +(transferred to + +Coenypha + +). + + + + + +Other material examined. + + +CHILE +: + +Bío-Bío + +: + +1j, +Concepción +( +Estero Nonguén +), +36°49’12.49”S +, +73°2’39.80”W +, + +05 October 1996 + +, T. +Cekalovic +( +MHNS +) + +; + +1♀ +, +Concepción +( +Periquillo +), +36°49’12.49”S +, +73°2’39.80”W +, + +16 March 1997 + +, +T. Cekalovic +( +MHNS +) + +. + + + +Los Ríos + +: + +3j, +Valdivia +( +Huachocopihue +), +39°50’2.23”S +, +73°14’17.32”W +, + +07 March 1965 + +, H. +Levi +( +MCZ +) + +. + + +Los Lagos + +: + +1♁ and + +1♀ +, +Osorno +( +Termas de Puyehue +), +40°43’16.58”S +, +72°19’3.85”W +, + +19–25 December 1982 + +, +A. Newton +& +M. Thayer +( +MHNS +) + +; + +2♀ +, +Osorno +( +Aguas Calientes +), +40°43’43.88”S +, +72°18’43.17”W +, + +13–17 December 1998 + +, +M. Ramírez +, +L.Compagnucci +, C. +Grismado +& L. +Lopardo +( +MACN-Ar +, +MACN-Ar 10423 +) + +; + +1♀ +, +Llanquihue +( +Puerto Montt +), +41°28’8.10”S +, +72°56’28.09”W +, + +February 1983 + +, +G. Arriagada +( +MHNS 715 +) + +; + +1♀ +, same locality and collector of the previous vial, + +24-29 January 1983 + +( +MHNS 725 +) + +; + +1♀ +, +Llanquihue +, +41°34’60.00”S +, +72°40’60.00”W +, + +23 November 1993 + +, +N. Platnick +& +M. Ramírez +( +MHNS +) + +; + +1♀ +, same locality of the previous vial, + +April 1989 + +, L. +Peña +( +MHNS +) + +; + +1♀ +and 1♁, +Chamisa +, +41°15’38.27”S +, +73°0’28.23”W +, + +13 December 1981 + +, +L Peña +( +MCZ +) + +; + +1♁, +Isla Grande de Chiloé +( +Huequetrumao +), +42°27’22.52”S +, +73°52’47.36”W +, + +27 December 1981 + +, L. +Peña +( +MHNS +) + +; + +1♀ +, +Isla Grande de Chiloé +( +Puente La Caldera +), +42°37’26.28”S +, +73°55’35.66”W +, + +18 February 1997 + +, T. +Cekalovic +( +MHNS +) + +; + +1♁, +Isla Grande de Chiloé +( +Lago Huillinco +), +42°41’45.02”S +, +73°55’52.42”W +, + +12-22 December 2002 + +, M. +Thayer +& A. +Newton +( +MHNS 2857855 +) + +; + +1♀ +and 1j, +Isla Quinchao +, +42°28’9.00”S +, +73°30’53.00”W +, + +19 February 1997 + +, +T. Cekalovic +( +MHNS +) + +; + +1 ♀ +, +La Junta +[ +43°58’20.78”S +, +72°24’12.63”W +, +Aysén +( +MHNS +). + + + + + +Diagnosis. +Females of + +C. antennata + +are similar to those of + +C. nodosa + +by the presence of a pair of stout and conical projections on the posterior portion of the opisthosoma ( +Figs 4A +, +12A +), caudal region well-developed and a strong spiniform macrosetae on the mesial prolateral surface of femora I. Nevertheless, they can be distinguished from this and other species of the genus by their narrow and longer cephalic portion and by the epigynum that looks like a “diving mask”, having a short and incomplete septum between the copulatory openings ( +Figs 4C, 4E +). Males of + +C. antennata + +are distinguished from those of + +C. nodosa + +by their stronger legs ( +Fig. 5A +), shorter embolus ( +Fig. 5C +) and RTAvbr close to the tip of the RTA, curving towards the axis of the latter ( +Figs 5E, 5F +). Both males and females present a diagnostic feature that apparently inspired the name of the species: a pair of strong macrosetae in the middle of the MOQ area that makes look that these spiders have antennas ( +Fig. 4B +). + + + + + +Description. +Female +(from Concepción, MHNS): + +Anterior eye row recurved and posterior row slightly recurved; ALE are twice the size of the AME ( +Figs 4A, B +). Prosoma and anterior legs (I and II) predominantly orange-brown with few darker spots (or stripes, in the case of the carapace); legs III and IV brown, except for the tarsi and the proximal region of the femora, that are lighter ( +Fig. 4A +). Opisthosoma yellowish with a median brown taint on the dorsum, splitting posteriorly along the abdominal projections ( +Fig. 4A +). Copulatory ducts wide, short and sclerotized; spermathecae irregularly globose, with a median narrowing and apical PG ( +Fig. 4D +). Measurements: eye diameters and interdistances: AME 0.08, ALE 0.17, PME 0.17, PLE 0.17, AME-AME 0.13, AME-ALE 0.11, PME-PME 0.15, PME-PLE 0.13. MOQ length 0.44, MOQ posterior width 0.49, MOQ anterior width 0.28; leg formula: 1243: leg I—femur 2.63/ patella 1.25/ tibia 1.99/ metatarsus 1.63/ tarsus 0.79/ total 8.29; II—2.12/ 1.13/ 1.63/ 1.44/ 0.66/ 6.98; III—1.38/ 0.76/ 1.08/ 0.83/ 0.59/ 4.64; IV—1.78/ 0.77/ 1.31/ 1.05/ 0.61/ 5.52. Prosoma length 2.76, width 2.39, opisthosoma length 3.55, total body length 6.31; clypeus height 0.29, sternum length 1.24, width 1.17, endites length 0.65, width 0.32, labium length 0.34, width 0.48. + + + +Male +(FMNH 2857855): + +Eyes as in the female. Prosoma dark-brown, anterior legs (I and II) brown and posterior ones (III and IV) brown with darker spots on tibiae and on the distal portion of femora ( +Figs 5A, B +). Opisthosoma greyish-brown on the median portion of the dorsum, from its anterior margin until the spinnerets, and yellow on the sides ( +Fig. 5A +). Palp with many tibial setae; embolus rests behind the tegulum and it is relatively short when compared to those of the males of other congeneric species ( +Figs 5C, E +). Measurements: eye diameters and interdistances: AME 0.09, ALE 0.19, PME 0.17, PLE 0.17, AME-AME 0.14, AME-ALE 0.13, PME-PME 0.19, PME-PLE 0.12. MOQ length 0.48, MOQ posterior width 0.56, MOQ anterior width 0.34; leg formula: 1243: leg I—femur 2.72/ patella 1.25/ tibia 2.19/ metatarsus 1.87/ tarsus 1.05/ total 9.08; II—2.32/ 1.09/ 1.78/ 1.55/ 0.82/ 7.56; III—1.52/ 0.74/ 1.14/ 0.94/ 0.65/ 4.99; IV—1.97/ 0.88/ 1.34/ 1.04/ 0.75/ 5.98. Prosoma length 2.71, width 2.51, opisthosoma length 2.82, total body length 5.53; clypeus height 0.35, sternum length 1.16, width 1.14, endites length 0.67, width 0.34, labium length 0.35, width 0.50. + + + + +Distribution. +CHILE +: +Bío-Bío +, +Los Rios +, +Los Lagos +and +Aysén +( +Fig. 14 +). + + + + \ No newline at end of file diff --git a/data/38/5B/87/385B87CBFFE8D069FF47FED434E86822.xml b/data/38/5B/87/385B87CBFFE8D069FF47FED434E86822.xml new file mode 100644 index 00000000000..deb5b080197 --- /dev/null +++ b/data/38/5B/87/385B87CBFFE8D069FF47FED434E86822.xml @@ -0,0 +1,229 @@ + + + +Taxonomic review of the Andean crab spiders genus Coenypha Simon, 1895 (Thomisidae: Stephanopinae) + + + +Author + +Machado, Miguel + + + +Author + +Previato, Thales + + + +Author + +Grismado, Cristian J. + + + +Author + +Teixeira, Renato + +text + + +Zootaxa + + +2023 + +2023-06-21 + + +5306 + + +3 + + +301 +330 + + + + +http://dx.doi.org/10.11646/zootaxa.5306.3.1 + +journal article +53769 +10.11646/zootaxa.5306.3.1 +0c0b9965-f8a4-4ac8-b84c-f4589d3d79f0 +1175-5326 +8062920 +C1379C64-6C6B-4784-B9E4-6433319EAE3C + + + + + + + +Coenypha +Simon, 1895 + + + + + + + + + + +Thomisus +Nicolet, 1849: 391 + + +, pl. 3, fig. 7; 392, pl. 3, figs 8, 11 (in part). + + + + + + +Stephanopis +Keyserling, 1880: 187 + + +, pl 4, fig 103 (in part). + + + + + + +Coenypha +Simon, 1895: 1051 + + +; 1053, fig. 1090. Mello-Leit„o 1926: 322, fig. 43; + +Machado & Teixeira 2021: 296 + +. + + + + + + +Type +species: + + +Coenypha edwardsi +( +Nicolet, 1849 +) + + + + + +Diagnosis. +See +Machado and Teixeira (2021: 296) +. + + + + +Description. +Medium-sized spiders with marked sexual size dimorphism (total length +3.75–4.44 in +males, +6.55–8.60 in +females) and cryptic coloration, varying from yellow to dark brown ( +Figs 1A–E +). Prosoma wider than long, presenting rough texture, many hyaline setae, and sparse clavated ones. Opisthosoma trapezoidal with anterior border varying from straight to deeply excavated ( +Figs 1 A–E +). Tibiae I bear four pairs of ventral macrosetae, while tibiae II present only three pairs equally distant; posterior legs (III and IV) very reduced, with dense tarsal scopula. Epigynum with membranous and coiled copulatory ducts ( +Fig. 2F +); spermathecae subdivided in small chambers ( +Figs 2D, 2F +); male palp with discoid tegulum, pointed RTA and RTAvbr short, truncated or acute; embolus long, flattened, ribbon-shaped and presenting hyaline pars pendula ( +Figs 3C–F +). + + +Composition. +Six species distributed along the southern Andes and Patagonia regions: + +Coenypha edwardsi +( +Nicolet, 1849 +) + +, + +Coenypha antennata +( +Tullgren, 1902 +) + +, + +Coenypha ditissima +( +Nicolet, 1849 +) + +, + +Coenypha trapezium + + +sp. nov. + +, + +Coenypha foliacea + + +sp. nov. + +and + +Coenypha nodosa +( +Nicolet, 1849 +) + +. + + +Note. +The new species + +Coenypha trapezium + + +sp. nov. + +and + +Coenypha foliacea + + +sp. nov. + +are described based on males and females. However, for these two species there are still no records of both sexes collected together or in the same/near locality. Therefore, they were tentatively matched based on color patterns, shape and number of abdominal projections and disposition of tibial macrosetae. + + +We believe that proposing here what can be seen as doubtful associations is yet preferable than create unnecessary new names. Moreover, we take the opportunity to include them in this broader approach on + +Coenypha + +, avoiding isolated taxonomic notes or smaller papers on new species that would likely have less appeal and impact as a research publication. + + + + \ No newline at end of file diff --git a/data/38/5B/87/385B87CBFFE8D06FFF47FAC831E26A4E.xml b/data/38/5B/87/385B87CBFFE8D06FFF47FAC831E26A4E.xml new file mode 100644 index 00000000000..af29a8e2b48 --- /dev/null +++ b/data/38/5B/87/385B87CBFFE8D06FFF47FAC831E26A4E.xml @@ -0,0 +1,1477 @@ + + + +Taxonomic review of the Andean crab spiders genus Coenypha Simon, 1895 (Thomisidae: Stephanopinae) + + + +Author + +Machado, Miguel + + + +Author + +Previato, Thales + + + +Author + +Grismado, Cristian J. + + + +Author + +Teixeira, Renato + +text + + +Zootaxa + + +2023 + +2023-06-21 + + +5306 + + +3 + + +301 +330 + + + + +http://dx.doi.org/10.11646/zootaxa.5306.3.1 + +journal article +53769 +10.11646/zootaxa.5306.3.1 +0c0b9965-f8a4-4ac8-b84c-f4589d3d79f0 +1175-5326 +8062920 +C1379C64-6C6B-4784-B9E4-6433319EAE3C + + + + + + + +Coenypha edwardsi +( +Nicolet, 1849 +) + + + + + + + +Figs 1A–E +, +2A–F +, +3A–F +, +14A + + + + + + + +Thomisus edwardsii + +Nicolet, 1849: 392 + + + +, pl. 3, figs 8, 11 ( +syntypes +, female and male from +Chile +, +Valdivia +, not found in MNHN, + +probably lost, not examined). + + + +Thomisus lucasi +Nicolet, 1849: 391 + +( +syntypes +, +2 females +from +Chile +, Valdivia [MNHN 3392], examined). +New Synonymy. + + + +Thomisus fuliginosus +Nicolet, 1849: 392 + +( +syntypes +, +1 male +and +8 juveniles +from +Chile +[MNHN 6967], examined). +New +Synonymy. + + + +Stephanopis edwardsi +Keyserling, 1880: 187 + +, pl. 4, fig. 103. + + + +Coenypha edwardsi +: +Simon, 1895: 1053 + +, fig. 1090. + + + +Coenypha lucasi +: +Simon, 1895: 1051 + +. + + + +Coenypha edwardsi +: +Simon, 1895: 1051 + +. + + + +Coenypha fasciata +Mello-Leit + +„o, 1926: 322, fig. 43 ( +holotype +female from +Chile +, Valdivia [MNHN 18242a], examined). +New +Synonymy. + + + + +Note: +Although +Nicolet (1849) +did not designate any +type +specimen, most species of + +Thomisus + +described by him from +Chile +were found at MNHN. However, this is not the case with + +C. edwardsi + +. Thus, we identify the species by the comparison of several specimens from Valdivia, +Chile +, with the original description and illustrations provided by +Nicolet (1849) +.The description shows a female with an abdomen in light colors, trapezoid-shaped, with an arched posterior margin; while the male shows a dark spot in the posterior part of the abdomen and with a sinuous posterior margin [in the original: “...ondulaciones del borde posterior...”]. Spiders with these features were examined and showed no relevant differences regarding their genital features in comparison to other specimens recognized as + +T. lucasi + +and + +T. fuliginosus + +(species also described by +Nicolet 1849 +and deposited at MNHN, examined here). We settle the priority of + +T. edwardsi + +over + +T. lucasi + +, and + +T. fuliginosus + +(ICZN 2.4.2.1 and 2.4.2.2.) because the first name was the most used in the literature. Additionally, the synonymy of + +C. fasciata + +is also proposed by the absence of significative differences with the Nicolet species. + + + + +Other material examined. + + +CHILE +: + +Valparaíso + +: + +1♀ +, +Petorca +, +La Ligua +, +32°27’9.72”S +, +71°13’31.45”W +, + +27 September 1980 + +( +AMNH +) + +; + +1j, +Viña del Mar +, +32°59’40.93”S +, +71°32’33.68”W +, + +04 December 1982 + +, M. +Pino +( +MHNS 862 +) + +; + +1♀ +, +Granizo +, +32°58’58.96”S +, +71°10’45.12”W +, + +October 1982 + +, +M. Pino +( +MHNS 632 +) + +; + +1♁, same locality and collector of the previous vial, + +18 December 1983 + +( +MHNS 919 +) + +; + +1♀ +, +Quintero +, +33°2’49.45”S +, +71°35’23.18”W +, + +12 December 1980 + +, +L. Peña +( +AMNH +) + +. + + + +Coquimbo + +: + +1♁, +Ovalle +, +30°36’15.66”S +, +71°11’49.19”W +, + +01 December 1950 + +, +Ross +& +Michelbacher +( +CAS 9072303 +) + +. + + + +Santiago + +: + +1j, +Cajón del Rio Maipo +, +33°47’53.86”S +, +70°51’52.50”W +, + +November 1984 + +, G. +Arriagada +( +MHNS 892 +) + +; + +1♀ +, +Pudahuel +( +Parque Laguna Carén +), +33°25’51.39”S +, +70°50’24.79”W +, same collector and date of the previous vial ( +MHNS 881 +) + +; + +1♀ +and 2j, +Quilicura +, +33°21’27.63”S +, +70°43’45.38”W +, + +May 1979 + +, +L. Peña +( +AMNH +) + +; + +1♁ and 2j, +Cerro Manquehue +, +33°21’3.00”S +, +70°34’56.01”W +, + +August 1979 + +, +L. Peña +( +AMNH +) + +; + +1♀ +, +Cordoba Coast +, +33°26’56.00”S +, +70°40’9.35”W +, + +15–20 February 1979 + +, +L. Peña +( +AMNH +) + +; + +6♁, +2♀ +and 7j, +Cuesta La Dormida +, +33°31’16.74”S +, +70°47’42.40”W +, + +13–18 November 1982 + +, L. +Peña +( +AMNH +) + +; + +1♀ +and 1j, +Pirque +, +33°41’14.91”S +, +70°35’18.17”W +, + +30 November 1982 + +( +AMNH +) + +. + + +Talca + +: + +1♁, + +Maule +, +35°25’23.68”S +, +71°38’54.53”W +, + +22 December 1950 + +, +Ross +& +Michelbacher +( +CAS 9046659 +) + +. + + + +Bio-Bío + +: + +1♀ +, +Ñuble +(40 +Km +from +Coihueco +), +36°37’45.12”S +, +71°49’57.81”W +, + +15 February 2005 + +, +M. Ramírez +& +F. Labarque +( +MACN-Ar 27638 +) + +; + +1♁, +Concepción +( +Palo Grande +), +36°48’46.51”S +, +73° 1’4.14”W +, + +29 December 1996 + +, +T.Cekalovic +( +AMNH +) + +; + +2j, +Concepción +( +Camino Chome Ramuntcho +), +36°49’8.18”S +, +73° 3’1.15”W +, + +08 November 1996 + +, +T. Cekalovic +( +AMNH +) + +; + +1♁, +Ñuble +( +Recinto +), +36°41’59.98”S +, +71°53’38.73”W +, + +01–03 October 1983 + +, +L. Peña +( +AMNH +) + +; + +1♁, +Concepción +( +Periquillo +), +36°55’53.72”S +, +73° 0’33.94”W +, + +16 March 1997 + +, +T. Cekalovic +( +AMNH +) + +; + +1♁, +Concepción +( +Estero Nonquen +), +36°49’14.35”S +, +73° 0’55.31”W +, + +11 November 1996 + +, +T. Cekalovic +( +AMNH +) + +; + +1♁, 1#f and 4j, +Concepción +( +Lomas Colorada +), +36°50’54.14”S +, +73°7’59.64”W +, + +24 November 1996 + +, +T. Cekalovic +( +AMNH +) + +. + + + +Araucanía + +: + +1j, +Malleco +, +38°9’48.82”S +, +72°31’13.74”W +, + +February 1965 + +, +Fritz +( +MACN-Ar 18678 +) + +; + +4♀ +, same locality of the previous vial, + +November 1979 + +, L. +Peña +( +AMNH +) + +; + +1♀ +, +Angol +, +37°48’21.87”S +, +72°42’13.70”W +, 1950, +S. Bullock +( +CAS 9046660 +) + +; + +1♀ +, same locality of the previous vial, + +29 January 1951 + +, +Ross +& +Michelbacher +( +CAS 9072302 +) + +; + +2j, +Cautín +( +Chacamo +), +38°34’56.21”S +, +73° 3’11.75”W +, + +17–23 February 1981 + +, +L. Peña +( +AMNH +) + +. + + + +Los Rios + +: + +2j, +Valdivia +, +39°49’2.59”S +, +73°14’33.12”W +, no collection date ( +MHNS 18242 +) + +; + +1♀ +, +Valdivia +, +39°49’2.65”S +, +73°14’33.07”W +, + +12 October 1976 + +, +E. Krahmer +( +MCZ 133392 +) + +; + +2♁, +2♀ +1j; 1983 ( +MHNS 802 +) + +; + +1#, +2♀ +and 1j; 1984 ( +MHNS 840 +) + +; + +1♁ and 6j; + +15 January 1951 + +, +Ross +& +Michelbacher +( +CAS 9072304 +) + +; + +1j, + +10 January 1989 + +, M. +Ramírez +( +MACN 18680 +) + +; + +1♁ and 1j, +Enco River Region +, +39°54’39.75”S +, +72° 8’53.29”W +, + +3 March 1955 + +, L. +Peña +( +MACN-Ar 9539 +) + +. + + + +Los Lagos + +: + +1♁ and 2j, +Lepihue +, +39°50’38.25”S +, +73°13’53.43”W +, + +21 January 1951 + +, +Ross +& +Michelbacher +( +CAS 9072300 +) + +; + +1♁ and 1j, +Osorno +( +Salto Pilmaiquén +), +40°38’50.88”S +, +72°39’26.90”W +, + +27 January 1951 + +, +Ross +& +Michelbacher +( +CAS 9072301 +) + +; + +3j, +Osorno +( +Puyehue +), +40°43’43.88”S +, +72°18’43.16”W +, + +13–17 December 1998 + +, +M. Ramírez +, +L. Compagnucci +, C. +Grismado +& L. +Lopardo +( +MACN-Ar 18676 +) + +; + +1j, +Llanquihue +, +41°2’44.04”S +, +72°55’22.32”W +, + +12 November 1994 + +, +R. Leschen +& +C. Carlton +( +AMNH +) + +; + +4♁, +Petrohue +, +41°8’27.52”S +, +72°24’28.23”W +, + +29 March 1968 + +, +L. Peña +( +MCZ 133669 +) + +; + +1j, + +26 February 1972 + +, +Bondon +( +MACN-Ar 18679 +) + +; + +1♀ +, + +29 March 1968 + +, L. +Peña +( +MCZ 133408 +) + +; + +1♁ and 4j, +Puerto Montt +, +41°28’8.10”S +, +72°56’28.09”W +, + +24–29 January 1983 + +, +G. Arriagada +( +MHNS 728 +) + +; + +3j, + +30 January to 15 February 1983 + +( +MHNS 717 +) + +; + +1♀ +, ( +MHNS 710 +) + +; + +1♁, +Isla Chiloé +( +Butalcura +), +42°13’59.88”S +, +73°44’60.00”W +, + +21 February 1997 + +, +T. Cekalovic +( +AMNH +) + +; + +1♀ +, +Isla Chiloé +( +Dalcahue +), +42°22’29.25”S +, +73°39’6.35”W +, + +01 February 1981 + +, +L. Peña +( +AMNH +) + +; + +2♁, +Chiloé Province +, +42°22’39.47”S +, +73°39’6.78”W +, + +01–04 April 1968 + +, L. +Peña +( +MCZ 133665 +) + +; + +1♁, same locality and collector of the previous vial, + +February 1967 + +( +MCZ 133409 +) + +; + +1j, +Cole Cole +, +42°25’22.39”S +, +74° 4’58.62”W +, + +08–11 February 1991 + +, +M. Ramírez +( +MACN-Ar 18681 +) + +; + +1j, +Chepu +, +42°31’24.34”S +, +73°52’47.36”W +, + +30 January 1981 + +, +L. Peña +( +AMNH +) + +; + +1j, +Isla Quinchao +, +42°32’4.24”S +, +73°25’16.10”W +, + +19 February 1997 + +, +T. Cekalovic +( +AMNH +) + +; + +1♀ +, +Isla Chiloé +, +42°37’25.31”S +, +73°55’35.34”W +, + +19 February 1996 + +, +T. Cekalovic +( +AMNH +) + +; + +1♁ and 3j, same locality of the previous vial, + +01 February 1981 + +, L. +Peña +( +AMNH +) + +; + +4j, same locality of the previous vial, + +22 February 1997 + +, T. +Cekalovic +( +AMNH +) + +; + +1♀ +, +Huequetrumao +, +42°37’26.29”S +, +73°55’35.66”W +, + +27 December 1981 + +, +L. Peña +( +AMNH +) + +; + +1♁, +Isla Lemuy +( +Puerto Haro +), +42°38’19.00”S +, +73°38’32.36”W +, + +20 February 1996 + +, +T. Cekalovic +( +AMNH +) + +; + +1♀ +, +Santo Antonio de Chadmo +, +42°55’5.71”S +, +73°39’41.42”W +, + +08 February 2001 + +, T. +Cekalovic +( +FMNH 61793 +) + +; + +1♀ +, +Puerto Carmen +, +43°7’49.25”S +, +73°45’21.85”W +, + +15–19 March 1981 + +, +L. Peña +( +AMNH +) + +; + +4j, +Gicao +, +43°9’0.20”S +, +73°41’57.38”W +, + +February 1981 + +, +L. Peña +( +AMNH +) + +. +Magallanes +y + + + +Antártica +Chilena + +: + +1♀ +, +Puntarenas +, no collection date ( +MHNS 3406 +) + +. + + +ARGENTINA +: + +Chubut +: + + +Parque Nacional Lago Puelo +: Puerto, S 42.097946 ° W 71.620299 ° ( +Google Earth +), elev. + +210m + +( +Google Earth +), + +15 November 2022 + +, leg. technical personnel of +P. N. Lago Puelo +( +MACN-Ar 43771 +) + +. + + + + +Diagnosis. +Females of + +C. edwardsi + +resemble those of + +C. trapezium + + +sp. nov. +, + +both are the species with the most extreme cases of dorsoventrally compressed habitus of the genus ( +Figs 2B +, +8B +). Moreover, these two species have robust femora of legs I and II with a pair of apical projections ( +Figs 2A +, +8A +). However, + +C. edwardsi + +can be distinguished from + +C. trapezium + + +sp. nov. + +by the epigynal plate with oblique slits (feature that is more similar to what can be observed in + +C. ditissima + +) leading to the copulatory openings, and a flattened MSept ( +Fig. 2C +). The copulatory ducts run in two twists before getting to the spermathecae, which present an apical PG ( +Fig. 2D +). Males can be easily recognized and distinguished from its congeneric species by the shape of their opisthosoma (with eight tiny posterior projections) ( +Fig. 3A +). Their well-developed TRin apical position and long embolus ( +Fig. 3C +), are similar to those of the males of + +C. trapezium + + +sp. nov. + +( +Fig. 9C +), however, the male palp of + +C. edwardsi + +is unique by its conical RTA bearing a short and acute RTAvbr on its basis ( +Fig. 3D +). + + + + + +Description. +Female +(MHNS 840): + +Anterior eye row recurved and posterior row straight; ALE almost twice as large as the AME ( +Figs 2A, B +). Prosoma granulated, with many setiferous tubercles and hyaline setae; light brown, cephalic area and center of the thoracic portion dark brown ( +Fig. 2B +). Clypeus bears a pair of central macrosetae on its margin. Sternum brown, scutiform and slightly wider than long. Femora I brown, robust and presenting few setiferous tubercles on its dorsal and prolateral surface; anterior patellae, tibiae, and metatarsi (I and II) predominantly brown, dark brown on their dorsal surface; posterior legs entirely brown. Opisthosoma light brown with a transversal darker line; anterior border slightly concave and posteriorly beveled ( +Fig. 2A +). Epigynal plate with copulatory openings preceded by obliquely convergent slits and divided by a wide and flattened MSept ( +Fig. 2C +); copulatory ducts wrinkled, membranous and coiled (two twists); spermathecae kidney-shaped bearing a PG ( +Fig. 2D +). Measurements: eyes diameters and inter distances: AME 0.09, ALE 0.15, PME 0.12, PLE 0.12, AME-AME 0.18, AME-ALE 0.12, PME-PME 0.24, PME-PLE 0.14. MOQ length 0.44, MOQ posterior width 0.26, MOQ anterior width 0.20; leg formula: 1243: leg I—femur 5.60/ patella 2.35/ tibia 3.90/ metatarsus 2.25/ tarsus 1.50/ total 15.60; II—3.20/ 1.50/ 2.20/ 1.25/ 1.10/ 9.25; III—1.25/ 0.95/ 0.90/ 0.60/ 0.55/ 4.25; IV—1.55/ 0.95/ 1.10/ 0.60/ 0.55/ 4.75; total length 8.60, prosoma length 3.60, width 3.90, opisthosoma length 5.00, clypeus height 0.30, sternum length 1.46, width 1.59, endites length 0.82, width 0.46, labium length 0.52, width 0.70. + + + +Male +(CAS 9046659): + +Anterior eye row recurved and posterior slightly recurved ( +Figs 3A, B +). Prosoma and other ocular characteristics as in female. Sternum brown, scutiform and slightly wider than long. Legs I, II and IV predominantly brown, with randomly darker spots; legs III entirely yellow with few brown stains. Opisthosoma as in female, but less widened. Palp with oval cymbium, tegulum with an apical tegular ridge and no apophyses ( +Figs 3C, E +); palpal tibia bears three prolateral macrosetae, a short and conical RTAvbr and an acute RTA ( +Fig. 3D +). Measurements: eye diameters and interdistances: AME 0.06, ALE 0.12, PME 0.10, PLE 0.09, AME-AME 0.12, AME-ALE 0.08, PME-PME 0.16, PME-PLE 0.12. MOQ length 0.34, MOQ posterior width 0.24, MOQ anterior width 0.16; leg formula: 1234: leg I—femur 3.05/ patella 1.15/ tibia 2.25/ metatarsus 1.30/ tarsus 0.80/ total 8.55; II—1.48/ 0.64/ 1.12/ 0.70/ 0.58/ 4.52; III—0.76/ 0.48/ 0.62/ 0.39/ 0.36/ 2.61; IV—0.88/ 0.46/ 0.58/ 0.28/ 0.36/ 2.56; total length 4.44, prosoma length 1.94, width 2.00, opisthosoma length 2.50, clypeus height 0.22, sternum length 0.80, width 0.94, endites length 0.46, width 0.24, labium length 0.26, width 0.38. + + + + +Distribution. +CHILE +: +Coquimbo +, +Valparaíso +, +Santiago +, +Talca, Bío-Bío +, +Araucanía +, +Los Ríos +, and +Los Lagos +, +ARGENTINA +: +Chubut +( +Fig. 14A +). + + + + +Variation. + +C. edwardsi + +present a wide range of body coloration, varying from the most common morphotype, which was described above ( +Figs 1A, D +, +2A +), to specimens fully dark-brown and covered by light-colored setae ( +Fig. 1C +). Yellow individuals were also found ( +Fig. 1B +) as well as those that are predominantly whitish with sets of brown spots and stripes on their femora, median cephalic area, and opisthosoma ( +Fig. 1E +). + + + + \ No newline at end of file diff --git a/data/38/5B/87/385B87CBFFF1D070FF47FB62314A68C2.xml b/data/38/5B/87/385B87CBFFF1D070FF47FB62314A68C2.xml new file mode 100644 index 00000000000..b97273ec165 --- /dev/null +++ b/data/38/5B/87/385B87CBFFF1D070FF47FB62314A68C2.xml @@ -0,0 +1,118 @@ + + + +Taxonomic review of the Andean crab spiders genus Coenypha Simon, 1895 (Thomisidae: Stephanopinae) + + + +Author + +Machado, Miguel + + + +Author + +Previato, Thales + + + +Author + +Grismado, Cristian J. + + + +Author + +Teixeira, Renato + +text + + +Zootaxa + + +2023 + +2023-06-21 + + +5306 + + +3 + + +301 +330 + + + + +http://dx.doi.org/10.11646/zootaxa.5306.3.1 + +journal article +53769 +10.11646/zootaxa.5306.3.1 +0c0b9965-f8a4-4ac8-b84c-f4589d3d79f0 +1175-5326 +8062920 +C1379C64-6C6B-4784-B9E4-6433319EAE3C + + + + + + + +Stephanopis exigua +( +Nicolet, 1849 +) + +nomen dubium + + + + + + + + + +Thomisus exiguus +Nicolet, 1849: 401 + + +. +Syntypes +from +Chile +, deposited in MNHN (4173), examined. + +Ramírez 1989: 11 + +. + +Stephanopis exigua +(Nicolet) + +: + +Simon 1895: 1054 + +. + + + +Note. +The +syntypes +series is composed of 20 poorly preserved juveniles. As their conditions and the immatures state do not allow a reliable identification, we proposed this species as +nomen dubium +. + + + + \ No newline at end of file diff --git a/data/38/5B/87/385B87CBFFF1D070FF47FF6431FE6CE8.xml b/data/38/5B/87/385B87CBFFF1D070FF47FF6431FE6CE8.xml new file mode 100644 index 00000000000..71f71b782dd --- /dev/null +++ b/data/38/5B/87/385B87CBFFF1D070FF47FF6431FE6CE8.xml @@ -0,0 +1,121 @@ + + + +Taxonomic review of the Andean crab spiders genus Coenypha Simon, 1895 (Thomisidae: Stephanopinae) + + + +Author + +Machado, Miguel + + + +Author + +Previato, Thales + + + +Author + +Grismado, Cristian J. + + + +Author + +Teixeira, Renato + +text + + +Zootaxa + + +2023 + +2023-06-21 + + +5306 + + +3 + + +301 +330 + + + + +http://dx.doi.org/10.11646/zootaxa.5306.3.1 + +journal article +53769 +10.11646/zootaxa.5306.3.1 +0c0b9965-f8a4-4ac8-b84c-f4589d3d79f0 +1175-5326 +8062920 +C1379C64-6C6B-4784-B9E4-6433319EAE3C + + + + + + + +Sidymella badia +( +Keyserling, 1880 +) + +comb. nov. + + + + + + +Figs 15A–B + + + + + + + +Stephanopis badia + +Keyserling, 1880: 181 + + + +, fig. 99 (Female +syntype +from +Bogotá +, +Colombia +, deposited in BMNH 3481, examined) + + + +Note. +The presence of spiniform macrosetae on the mesial surface of femora I and the remarkable bifid opisthosoma ( +Fig. 15A +) allow us to propose the transfer of + +S. badia + +to the genus + +Sidymella +Strand, 1942 + +. + + + + \ No newline at end of file diff --git a/data/38/5B/87/385B87CBFFF9D07DFF47FC6937D46DFA.xml b/data/38/5B/87/385B87CBFFF9D07DFF47FC6937D46DFA.xml new file mode 100644 index 00000000000..c229dc01bc3 --- /dev/null +++ b/data/38/5B/87/385B87CBFFF9D07DFF47FC6937D46DFA.xml @@ -0,0 +1,327 @@ + + + +Taxonomic review of the Andean crab spiders genus Coenypha Simon, 1895 (Thomisidae: Stephanopinae) + + + +Author + +Machado, Miguel + + + +Author + +Previato, Thales + + + +Author + +Grismado, Cristian J. + + + +Author + +Teixeira, Renato + +text + + +Zootaxa + + +2023 + +2023-06-21 + + +5306 + + +3 + + +301 +330 + + + + +http://dx.doi.org/10.11646/zootaxa.5306.3.1 + +journal article +53769 +10.11646/zootaxa.5306.3.1 +0c0b9965-f8a4-4ac8-b84c-f4589d3d79f0 +1175-5326 +8062920 +C1379C64-6C6B-4784-B9E4-6433319EAE3C + + + + + + + +Coenypha foliacea +Machado & Grismado + +sp. nov. + + + + + + +Figs 10 A–F +, +11 A–D +, +14C + + + + +Type material: + + +Holotype +: + +female, +Cautín +: +Temuco +: +Cerro Ñielol +[ +38°56’56.12”S +, +72°19’52.01”W +, +Araucanía +, +Chile +], + +January 1989 + +, +M. Ramírez +( +MHNS 8375 +). + + + + + +Paratypes +: + +1 male +, +Monumento Natural Contulmo +[ +38°0’51.55”S +, +73°10’48.24”W +, Purén, Malleco,Aracucanía, +Chile +], + +19 December 1998 + +, +Ramírez, M. J. +; +Compagnucci, L. A. +; +Grismado, C. J. +& +Lopardo, L. +( +MACN-Ar 18705 +) + +; + +1 female +, +Cerro Ñielol +[ +38°43’27.08”S +, +72°35’18.33”W +, Temuco, Cautín, +Araucanía +, +Chile +], + +21January1991 + +, +E. Maury +( +MACN-Ar 18706 +) + +. + + +Other material examined. +Two immatures collected with the +holotype +, presumably belong to the same species ( +MHNS +). + + + + +Etymology. +The specific name derives from the latin word + +foliacea + +, which means “leaf-shaped”, referring to the shape of the opisthosoma of this species that, combined with the cryptic coloration of the individuals, resembles a dry leaf, adjective. + + + + +Diagnosis. +The females of + +C. foliacea + + +sp. nov. + +resemble those of + +C. ditissima + +by their relative body size and shape of opisthosoma, however, they can be easily recognized by their enlarged femora I bearing a pair of sockets each, accommodating two hyaline and plumose macrosetae ( +Fig. 10A +). The prosoma of + +C. foliacea + + +sp. nov. + +also differs from + +C. ditissima + +by its more flattened profile, while the epigynum has a wider septum, copulatory openings with narrower entrances, shorter copulatory ducts and larger spermathecae ( +Figs 10C‒D +). Males of + +C. foliacea + + +sp. nov. + +are recognized by the presence of a single prolateral macroseta on cymbium ( +Fig. 11C +), which also presents a retrolateral concavity/arching to accommodate the terminal portion of the embolus ( +Fig. 11D +), similar to what is observed in + +C. ditissima + +. However, in + +C. foliacea + + +sp. nov. + +the embolus is shorter and less coiled. + + + + + +Description. +Female +( +Holotype +MHNS 8375): + +Anterior eye row recurved and posterior row slightly recurved; MOQ area covered by many whitish setae ( +Figs 10A, B +). Prosoma light brown on the sides and darker on the median thoracic area and cephalic region ( +Fig. 10A +). Anterior legs (I and II) predominantly light-brown and posterior ones (III and IV) dark-brown from the distal portion of femora until the tarsi; proximal portion of femora yellowish ( +Fig. 10A +). Opisthosoma brown, flattened, with rounded anterior margin and two pairs of posterior projections ( +Fig. 10A +). Epigynal plate with wide posterior folds converging in the middle to form an intromittent MSept ( +Figs 10C, E +); copulatory ducts hyaline and membranous, leading to a pair of spermathecae with porous distributed on its anterior surface, not grouped on a specific region forming a PG ( +Figs 10D, F +). Measurements: eye diameters and interdistances: AME 0.07, ALE 0.12, PME 0.13, PLE 0.14, AME-AME 0.09, AME-ALE 0.05, PME-PME 0.10, PME-PLE 0.08. MOQ length 0.30, MOQ posterior width 0.33, MOQ anterior width 0.20; leg formula: 1243: leg I—femur 2.81/ patella 0.93/ tibia 1.45/ metatarsus 1.18/ tarsus 0.67/ total 7.04; II—2.64/ 0.74/ 1.14/ 0.95/ 0.65/ 6.12; III—1.06/ 0.62/ 0.71/ 0.53/ 0.50/ 3.42; IV—1.41/ 0.63/ 0.98/ 0.78/ 0.57/ 4.37. Prosoma length 2.11, width 2.08, opisthosoma length 2.63, total body length 4.74; clypeus height 0.25, sternum length 0.92, width 0.98, endites length 0.50, width 0.27, labium length 0.23, width 0.42. + + + +FIGURE 10. + +Coenypha foliacea + + +sp. nov. +, + +female (MHNS 8375). A–B habitus (A dorsal, B frontal); C, E epigyne ventral; D, F vulva dorsal. + + + + +FIGURE 11. + +Coenypha foliacea + + +sp. nov. +, + +male (MACN-Ar 18705). A–B habitus (A dorsal, B frontal); C–D left palp (C ventral, D retrolateral). + + + + +Male +( +Paratype +MACN-Ar 18705): + +Eyes as in the female. Prosoma and opisthosoma entirely dark-brown, anterior legs (I and II) brown, with tibiae slightly curved; leg III entirely yellow and leg IV yellow only on the proximal half of the femora, being the other podomeres dark-brown ( +Fig. 11A +). Opisthosoma similar to that of females ( +Fig. 11A +). Palp has a cymbium with projected apical portion and oval tegulum ( +Fig. 11C +); RTA is thin and acute, while the RTAvbr is conical and almost as long as the RTA ( +Fig. 11D +). Measurements: eye diameters and interdistances: AME 0.10, ALE 0.18, PME 0.15, PLE 0.19, AME-AME 0.13, AME-ALE 0.11, PME-PME 0.18, PME-PLE 0.13. MOQ length 0.41, MOQ posterior width 0.51, MOQ anterior width 0.33; leg formula: 1243: leg I—femur 3.15/ patella 1.27/ tibia 2.36/ metatarsus 1.77/ tarsus 0.91/ total 9.46; II—2.63/ 1.09/ 2.00/ 1.40/ 0.84/ 7.96; III—1.69/ 0.99/ 1.10/ 0.90/ 0.78/ 5.46; IV—2.01/ 0.90/ 1.33/ 0.96/ 0.74/ 5.94. Prosoma length 3.35, width 3.15, opisthosoma length 3.37, total body length 6.72; clypeus height 0.29, sternum length 1.33, width 1.30, endites length 0.78, width 0.40, labium length 0.44, width 0.57. + + + + +Distribution. +CHILE +: +Araucanía +( +Fig. 14C +). + + + + \ No newline at end of file diff --git a/data/38/5B/87/385B87CBFFFAD078FF47FB3D31E96E82.xml b/data/38/5B/87/385B87CBFFFAD078FF47FB3D31E96E82.xml new file mode 100644 index 00000000000..357b51102fe --- /dev/null +++ b/data/38/5B/87/385B87CBFFFAD078FF47FB3D31E96E82.xml @@ -0,0 +1,326 @@ + + + +Taxonomic review of the Andean crab spiders genus Coenypha Simon, 1895 (Thomisidae: Stephanopinae) + + + +Author + +Machado, Miguel + + + +Author + +Previato, Thales + + + +Author + +Grismado, Cristian J. + + + +Author + +Teixeira, Renato + +text + + +Zootaxa + + +2023 + +2023-06-21 + + +5306 + + +3 + + +301 +330 + + + + +http://dx.doi.org/10.11646/zootaxa.5306.3.1 + +journal article +53769 +10.11646/zootaxa.5306.3.1 +0c0b9965-f8a4-4ac8-b84c-f4589d3d79f0 +1175-5326 +8062920 +C1379C64-6C6B-4784-B9E4-6433319EAE3C + + + + + + + +Coenypha trapezium +Machado & Grismado + +sp. nov. + + + + + + +Figs 8 A–F +, +9 A–F +, +14C + + + + +Type material: + + +Holotype +: + +female, +Pucará +, +Lago Lácar +, +Parque Nacional Lanín +, +Neuquén +, +Argentina +[ca. +40° 9’50 S +, +71°38’ W +]., + +15 December 1965 + +, +A. Giai +( +MACN-Ar 18675 +). + + + + + +Paratypes +: + +1 male +, +Parque Nacional La Campana +[ +32°57’15.69”S +, +71°4’38.13”W +, Quillota, +Valparaíso +, +Chile +], + +29 December 2002 + +, +A. Newton +& +A. Solodovnikov +( +FMNH 2857851 +) + +; + +1 male +, +Cuesta La Dormida +[ +33°31’16.74”S +, +70°47’42.40”W +, +Santiago +, +Chile +], + +18 November 1982 + +, +L. Peña +( +AMNH +) + +. + + + + +Etymology. +The specific name derives from latin noun + +trapezium + +, as a reference to the shape of the opisthosoma of this species. Noun in apposition. + + + + +Diagnosis. +Females of + +C. trapezium + + +sp. nov. + +resemble those of + +C. edwardsi + +by their body size (being the two biggest species in the genus), wide and flattened opisthosoma, and by the enlarged anterior femora bearing apical projections ( +Figs 2A +, +8A +). However, + +C. trapezium + + +sp. nov. + +differs from this species by the yellowish body coloration, prosoma as long as wide (instead of wider than long in + +C. edwardsi + +), and opisthosoma bearing only two pairs of posterior-lateral projections ( +Figs 8A, B +) (instead of eight in + +C. edwardsi + +, +Fig. 2A +). They can also be distinguished from + +C. edwardsi + +and other species of the genus by the triple twisted copulatory ducts ( +Fig. 8D +); the slits leading to the copulatory openings, unlike those of + +C. edwardsi + +, are not oblique but arranged horizontally and bearing a thin and excavated MSept ( +Fig. 8C +). Males can be recognized by their long ventral macrosetae on the anterior tibiae and metatarsi (I and II), well-developed caudal region ( +Fig. 9A +) and RTAvbr truncated with a terminal concavity, ( +Fig. 9D +), instead of a conical apophysis observed in + +C. edwarsi + +( +Fig. 3D +). + + + + + +Description. +Female +( +Holotype +, MACN-Ar 18675): + +Anterior eye row recurved and posterior row straight; ALE almost twice as large as the AME ( +Figs 8A, B +). Prosoma uniformly orange, with few clavate setae on conical sockets; sternum orange, scutiform and as wide as long. Legs are predominantly orange with few sparse dark punctuations. Opisthosoma yellow with small black spots symmetrically arranged; anterior border straight and posterior with a median concavity and two posterior lateral projections ( +Fig. 8A +). Copulatory ducts membranous, spermathecae subdivided in two chambers and with no visible pore region ( +Fig. 8D +). Measurements: eye diameters eyes inter distances: AME 0.08, ALE 0.14, PME 0.14, PLE 0.14, AME-AME 0.14, AME-ALE 0.10, PME-PME 0.22, PME-PLE 0.14. MOQ length 0.44, MOQ posterior width 0.32, MOQ anterior width 0.24; leg formula: 1243: leg I—femur 4.20/ patella 1.78/ tibia 2.75/ metatarsus 1.68/ tarsus 1.00/ total 11.41; II—3.40/ 1.45/ 2.20/ 1.22/ 0.80/ 4.75; III—1.42/ 0.90/ 1.02/ 0.56/ 0.54/ 4.44; IV—1.74/ 0.92/ 1.22/ 0.62/ 0.54/ 5.04; total length 7.54, prosoma length 3.09, width 3.10, opisthosoma length 4.45, clypeus height 0.38, sternum length 1.36, width 1.33, endites length 0.72, width 0.34, labium length 0.46, width 0.52. + + + +FIGURE 8. + +Coenypha trapezium + + +sp. nov. + +, female (MACN-Ar 18675).). A–B habitus (A dorsal, B frontal); C, E epigyne ventral; D, F vulva dorsal. + + + + +FIGURE 9. + +Coenypha trapezium + + +sp. nov. +, + +male (FMNH 2857851). A–B habitus (A dorsal, B frontal); C–F left palp (C, E ventral, D, F retrolateral). + + + + +Male +( +Paratype +, FMNH-ISN 2857851): + +Anterior eye row recurved and posterior straight ( +Figs 9A, B +). Prosoma brown with darker stains randomly distributed, sternum brown, scutiform and slightly wider than long. Legs with the same coloration pattern as the prosoma, except for the femora IV, which are yellow on their proximal half ( +Fig. 9A +). Opisthosoma yellow with many dark clavate setae, differing from those of the female by having an additional round lobe right after the posterior abdominal projections ( +Fig. 9A +). Palp bears a discoid tegulum ( +Fig. 9C +), a sinuous, grooved and pointed RTA and a truncated RTAvbr with bulged tip ( +Fig. 9D +). Measurements: eye diameters and interdistances: AME 0.08, ALE 0.18, PME 0.12, PLE 0.06, AME-AME 0.10, AME-ALE 0.06, PME-PME 0.18, PME-PLE 0.12. MOQ length 0.40, MOQ posterior width 0.24, MOQ anterior width 0.20; leg formula: 1234: leg I—femur 3.04/ patella 1.20/ tibia 2.44/ metatarsus 1.46/ tarsus 0.84/ total 8.98; II—2.00/ 0.81/ 1.44/ 1.00/ 0.44/ 5.69; III—0.88/ 0.56/ 0.62/ 0.42/ 0.40/ 2.88; IV—1.16/ 0.60/ 0.81/ 0.50/ 0.44/ 3,51; total length 4.58, prosoma length 2.15, width 2.00, opisthosoma length 2.43, clypeus height 0.22, sternum length 0.90, width 0.98, endites length 0.50, width 0.28, labium length 0.26, width 0.40. + + + + +Distribution. +ARGENTINA +: +Neuquén +; +CHILE +: +Valparaíso +and +Santiago +( +Fig. 14C +). + + + + \ No newline at end of file diff --git a/data/38/5B/87/385B87CBFFFCD07CFF47FEF1303C6A96.xml b/data/38/5B/87/385B87CBFFFCD07CFF47FEF1303C6A96.xml new file mode 100644 index 00000000000..77e31461c2e --- /dev/null +++ b/data/38/5B/87/385B87CBFFFCD07CFF47FEF1303C6A96.xml @@ -0,0 +1,964 @@ + + + +Taxonomic review of the Andean crab spiders genus Coenypha Simon, 1895 (Thomisidae: Stephanopinae) + + + +Author + +Machado, Miguel + + + +Author + +Previato, Thales + + + +Author + +Grismado, Cristian J. + + + +Author + +Teixeira, Renato + +text + + +Zootaxa + + +2023 + +2023-06-21 + + +5306 + + +3 + + +301 +330 + + + + +http://dx.doi.org/10.11646/zootaxa.5306.3.1 + +journal article +53769 +10.11646/zootaxa.5306.3.1 +0c0b9965-f8a4-4ac8-b84c-f4589d3d79f0 +1175-5326 +8062920 +C1379C64-6C6B-4784-B9E4-6433319EAE3C + + + + + + + +Coenypha nodosa +( +Nicolet, 1849 +) + + + + + + + +Figs 12 A–F +, +13 A–F +, +14B + + + + + + + +Thomisus nodosus +Nicolet, 1849: 397 + + +. +Lectotype +female, here designated, together with an immature +paralectotype +from +Chile +, deposited in MNHN (4194) and other +two immatures +from +Chile +, deposited in MNHN (4191), examined. + +Ramírez 1989: 11 + +. + + + + + + +Thomisus pubescens +Nicolet, 1849: 398 + + +. +Holotype +female from +Chile +, deposited in MNHN (4179), examined. +Roewer 1955 +(declared +nomen dubium +, rejected here); + +Ramírez, 1989: 11 + +. +New Synonymy. + + + + + + +Thomisus spectrum +Nicolet, 1849: 400 + + +. +Holotype +female (together +two immatures +) from +Chile +, deposited in MNHN (4177), examined. +Roewer 1955 +(declared +nomen dubium +, rejected here); + +Ramírez 1989: 11 + +. +New Synonymy. + + + + + + +Thomisus verrucosus +Nicolet, 1849: 398 + + +(female +lectotype +here designated, and +one female +paralectotype +from Valdivia, +Chile +, deposited in MNHN 4174, examined; +two males +found in the vial are misidentified + +Ozyptila +, + +see below). + +Ramírez 1989: 11 + +. +New Synonymy. + + + + + +Stephanopis nodosa +(Nicolet) + +: + +Simon 1895: 1054 + +; + +Machado and Teixeira 2021: 296 + +(transfer to + +Coenypha + +). + + + + + +Stephanopis verrucosa +(Nicolet) + +: + +Simon 1895: 1054 + +. + + + + +Stephanopis hystrix +Mello-Leit + +„o, 1951: 333, fig. 8. +Holotype +female from +Maullín +, +Llanquihue +, +Chile +, deposited in MNRJ, examined (lost in the fire). +New Synonymy. + + + + +Note. +In the case of + +T. nodosus + +, the material was found in two vials: MNHN 4191 with +two immatures +, and MNHN 4194 with a female and an immature. The female in the vial MNHN 4194 was treated as a +holotype +by +Machado & Teixeira (2021) +, which was a clear mistake once it was ignoring recommendation 73F ( +ICZN 2022 +). The individuals should be treated as +syntypes +followed by designation of +lectotype +, what we now do here. Nicolet described + +Thomisus nosodus + +based on a female and a male. The adult female examined in the type series fits with the description, but the other specimen is actually a juvenile. It is not clear if the juvenile was interpreted as a male by the author, so we chose to designate only the adult female as +lectotype +. The type series of + +T. verrucosus + +comprises four individuals of two different species. The females are conspecific with the +holotype +of + +C. nodosa +, + +but the males belong possibly to the genus + +Ozyptila +Simon, 1864 + +. Nicolet did not mention the sex of the specimen described, but the original text suggests that the author’s concept and diagnostic features of this species was based on a female: +“abdomen (…) terminado en punta” +(“pointed abdomen”), and also mentioned its similarity with + +T. nodosus + +. Here we settle the priority of + +T. nodosus + +over + +T. pubescens +, +T. spectrum +, + +and + +T. verrucosus + +(ICZN 24.2.1 and 24.2.2.). + + +Concerning the +two males +stored together with the +lectotype +female of + +T. verrucosus + +in MNHN 4174, their somatic and genital features correspond with those of the subfamily +Thomisinae +. The ocular arrangement with the MOQ area wider on its anterior portion, legs I and II short and robust, and tibiae I and II bearing two pairs of ventral macrosetae, match with the updated diagnosis of + +Ozyptila +Simon, 1864 + +, provided by +Almquist (2006) +. The palpal tibiae bearing two apophyses ( +VTA +and RTA) and a tegular apophysis, as well as the prosoma with a whitish dorsal median band and the opisthosoma narrowed anteriorly and wide on its posterior portion, are also similar to those of males of + +Ozyptila + +. We are unable to determine their specific identification or even if the material came from +Chile +since none native + +Ozyptila + +was recorded in South America until now. Once the name + +Thomisus verrucosus + +has been kept valid for the female, we chose to consider the male specimens wrongly assigned. + + +Other material examined. + + +ARGENTINA +: + +Chubut + +: + +2 ♀ +and 9j, +Lago Puelo +, +42° 5’50.9”S +, +71°36’14.09”W +, + +11–12 December 2021 + +, +M. Pacheco +, +L. Piacentini +& E. +Soto +( +MACN-Ar 42756–427558 +) + +; + +4♀ +and 29j, +42°5’49.2”S +, +71°36’44.2”W +, same collector and date of the previous vial ( +MACN-Ar 42753–42755 +) + +. + + +CHILE +: + +Bío-Bío + +: + +1j, +Ñuble +, +36°42’16.20”S +, +71°36’9.60”W +, + +15 February 2005 + +, +M. Ramírez +& +F. Labarque +( +MACN-Ar 10865 +) + +; + +2♀ +, +Concepción +( +Chome +), +36°42’52.73”S +, +73°8’21.39”W +, + +07 December 1995 + +, +T. Cekalovic +( +AMNH +) + +; 1♁ and + +1♀ +, +Concepción +( +Hualpén +), +36°47’12.03”S +, +73°6’35.83”W +, + +11 January 1989 + +, +M. Ramírez +( +MACN-Ar 18702–18703 +) + +; + +1♀ +, +Concepción +, +36°49’12.49”S +, +73°2’39.80”W +, + +14 January 1977 + +, +T. Cekalovic +( +MCZ 133404 +) + +; + +1♀ +and 1j, +Concepción +( +Estero Nonguén +), +36°49’41.25”S +, +73°0’19.52”W +, + +02 November 1996 + +, +T. Cekalovic +( +AMNH +) + +; 1♁ and + +1♀ +, +Concepción +, +36°50’37.1”S +, +73°02’17.6”W +, + +15 February 2005 + +, +M. Ramírez +& +F. Labarque +( +MACN-Ar 37308 +) + +; + +1♀ +, +Escuadrón +, +36°58’55.02”S +, +73°9’12.86”W +, + +15 November 1996 + +, +T. Cekalovic +( +AMNH +) + +. + + + +Araucanía + +: + +1♁, +Malleco +( +Monumento Natural Contulmo +), +38°00’46.8”S +, +73°11’15.4”W +, + +10–11 February 2005 + +, +M. Ramírez +& +F. Labarque +( +MACN-Ar 39685 +) + +; + +7j, +Malleco +( +Monumento Natural Contulmo +), +38°0’51.55”S +, +73°10’48.24”W +, + +19–21 December 1998 + +, +M. Ramírez +, +L. Compagnucci +, C. +Grismado +& L. +Lopardo +( +MACN-Ar 18709 +) + +. + + + +Los Ríos + +: + +4♀ +and 8j, +Valdivia +, +39°49’6.53”S +, +73°14’37.94”W +, 1984, +E. Krahmer +( +MHNS +) + +; 1♁ and + +1♀ +, same locality and collector of the previous vial, + +December 1982 + +( +MHNS 841 +) + +; + +1♀ +and 2j, same locality and collector of the previous vial, 1983 ( +MHNS 800 +) + +; + +1j, +Valdivia +( +Huachocopihue +), +39°50’2.23”S +, +73°14’17.32”W +, + +07 March 1965 + +, +H. Levi +( +MCZ 133400 +) + +. + + + +Los Lagos + +: + +1♀ +and 1j, +Osorno +( +Pucatrihue +), +40°32’6.87”S +, +73°42’31.82”W +, + +March 1968 + +, +L. Peña +( +MCZ 133406 +) + +; + +1♀ +and 4j, +Osorno +(20 +Km East of Puyehue +), +40°34’34.28”S +, +73°6’53.81”W +, + +25 January 1951 + +, +Ross +& +Michelbacher +( +CAS 9071270 +) + +; + +3j, +Osorno +( +Termas de Puyehue +), +40°40’0.00”S +, +71°13’60.00”W +, + +30 November 1994 + +, +R. Leschen +& +C. Carlton +( +AMNH +) + +; + +2j, +Osorno +( +Parque Nacional Puyehue +), +40°43’16.56”S +, +72°19’3.87”W +, + +19–26 December 1982 + +, +A. Newton +& +M. Thayer +( +AMNH +) + +; + +7j, +Osorno +( +Aguas Calientes +), +40°43’43.88”S +, +72°18’43.16”W +, + +13–17 December 1998 + +, +M. Ramírez +, +L. Compagnucci +, C. +Grismado +& L. +Lopardo +( +MACN-Ar 18662 +) + +; + +4j, +Llanquihue +( +Los Muermos +), +41°23’57.87”S +, +73°27’53.97”W +, + +19 January 1951 + +, +Ross +& +Michelbacher +( +CAS 9071273 +) + +; + +1j, +Isla Grande de Chiloé +( +Cole Cole +), +42°25’22.39”S +, +74°4’58.62”W +, + +08–11 February 1991 + +, +M. Ramírez +( +MACN-Ar 18648 +) + +; + +2♀ +and 2j, +Isla Grande de Chiloé +, +42°37’26.29”S +, +73°55’35.66”W +, + +22 February 1997 + +, T. +Cekalovic +( +AMNH +) + +; + +1j, +Palena +( +Chaitén +), +42°54’41.51”S +, +72°42’56.30”W +, + +04 December 1981 + +, +N. Platnick +and +R.T. Schuh +( +AMNH +) + +. + + + + +Diagnosis. + +C. nodosa + +resembles + +C. antennata + +in the shape of the opisthosoma, with a posterior pair of projections and protruding caudal region ( +Fig. 12A +), but + +C. nodosa + +differs from its closest related species in lacking the long pair of macrosetae between the ALE ( +Fig. 12B +); further, the prosoma is as wide as long, with cephalic portion shorter, while the epigynal plate presents a stout and complete MSept that separate the copulatory openings completely ( +Figs 12C, E +). If we can compare the shape of the epigynal plate of + +C. antennata + +with a diving mask ( +Figs 4C, E +), the epigynum of + +C. nodosa + +resembles a bear snout ( +Figs 12C, E +). Males can be distinguished by their long and thin legs with many needle-shaped setae ( +Fig. 13A +), flattened cymbium in retrolateral view ( +Fig. 13F +) and wide and hyaline pars pendula ( +Fig. 13E +). Unlike in + +C. antennata + +males, in which the embolus emerges from the tegulum in a basal position close to the tibia, in + +C. nodosa + +the embolus starts apically, and encircles the tegulum clockwise, its first ¼ can be observed in retrolateral view ( +Figs 13D, F +). + + + + + +Description. +Female +(MCZ 133404): + +Anterior eye row strongly recurved and posterior row slightly recurved; ALE have twice the diameter of the AME ( +Figs 12A, B +). Prosoma brown with a median longitudinal darker stain; all legs are predominantly brownish-yellow with dark-brown spots randomly distributed, except for the tibiae and metatarsi I and II, which are almost entirely dark-brown ( +Fig. 12A +). Opisthosoma brownish-yellow with darker spots on the median portion of the dorsum and on the sides of the caudal region ( +Fig. 12A +). Epigynal plate in ventral view resembles a “bear snout” ( +Figs 12C, E +); copulatory ducts are long, coiled and hyaline, leading to a pair of spermathecae with nodose exterior surface ( +Figs 12D, F +). Measurements: eye diameters and interdistances: AME 0.10, ALE 0.20, PME 0.20, PLE 0.22, AME-AME 0.18, AME-ALE 0.14, PME-PME 0.24, PME-PLE 0.16. MOQ length 0.58, MOQ posterior width 0.65, MOQ anterior width 0.40; leg formula: 1243: leg I—femur 3.78/ patella 1.76/ tibia 3.01/ metatarsus 2.17/ tarsus 1.14/ total 11.86; II—3.32/ 1.50/ 2.42/ 2.19/ 0.95/ 10.38; III—1.98/ 1.00/ 1.54/ 1.39/ 0.80/ 6.71; IV—2.57/ 1.10/ 1.88/ 1.66/ 0.83/ 8.04. Prosoma length 3.53, width 3.23, opisthosoma length 3.84, total body length 7.37; clypeus height 0.43, sternum length 1.55, width 1.43, endites length 0.88, width 0.44, labium length 0.53, width 0.63. + + + +Male +(MHNS 691): + +Eyes as in the female; prosoma entirely brown and legs predominantly dark-yellow, with few darker spots randomly distributed ( +Figs 13A, B +). Opisthosoma greyish-brown with a median darker taint on the median area of the dorsum ( +Fig. 13A +). Palpi have a short and obtuse RTA and a strongly sclerotized squared RTAvbr ( +Fig. 13D +); tegulum relatively small, oval-shaped and embolus with well-developed pars pendula ( +Fig. 13C +). Measurements: eye diameters interdistances: AME 0.10, ALE 0.21, PME 0.18, PLE 0.19, AME-AME 0.14, AME-ALE 0.11, PME-PME 0.19, PME-PLE 0.11. MOQ length 0.49, MOQ posterior width 0.45, MOQ anterior width 0.31; leg formula: 1243: leg I—femur 3.81/ patella 1.43/ tibia 3.53/ metatarsus 3.43/ tarsus 1.46/ total 13.66; II—3.38/ 1.25/ 2.90/ 2.71/ 1.35/ 11.59; III—1.76/ 0.80/ 1.49/ 1.28/ 0.81/ 6.14; IV—2.25/ 0.90/ 1.73/ 1.49/ 0.82/ 7.19. Prosoma length 2.61, width 2.41, opisthosoma length 2.73, total body length 5.34; clypeus height 0.27, sternum length 1.20, width 1.15, endites length 0.68, width 0.35, labium length 0.33, width 0.51. + + + + +Distribution. +ARGENTINA +: +Chubut +; +CHILE +: +Bío-Bío +, +Araucanía +, +Los Rios +and +Los Lagos +( +Fig. 14B +). + + + + \ No newline at end of file diff --git a/data/38/5B/B0/385BB02BFC1ED7C2DE04DC0661833EF1.xml b/data/38/5B/B0/385BB02BFC1ED7C2DE04DC0661833EF1.xml new file mode 100644 index 00000000000..5b29748bdec --- /dev/null +++ b/data/38/5B/B0/385BB02BFC1ED7C2DE04DC0661833EF1.xml @@ -0,0 +1,71 @@ + + + +Checklist of British and Irish Hymenoptera - Braconidae + + + +Author + +Broad, Gavin R. + + + +Author + +Shaw, Mark R. + + + +Author + +Godfray, H. Charles J. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8151 +8151 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8151 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8151 +1314-2828--8151 + + + + +Phaedrotoma curvata (Fischer, 1957) + + + + +Opius curvatus +Fischer, 1957 + + + +Distribution +Scotland + + +Notes + +added by +Godfray (1986) + + + + \ No newline at end of file diff --git a/data/38/5B/B8/385BB82D1DBB8FBE6E669D2C4C804455.xml b/data/38/5B/B8/385BB82D1DBB8FBE6E669D2C4C804455.xml new file mode 100644 index 00000000000..1794f399f98 --- /dev/null +++ b/data/38/5B/B8/385BB82D1DBB8FBE6E669D2C4C804455.xml @@ -0,0 +1,602 @@ + + + +Info Flora Schweiz - Poaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/poaceae.html + +url + + + + + +Melica ciliata +L. + + + + + +Wimper-Perlgras + + + + +Art ISFS: 256800 Checklist: 1028680 +Poaceae +Melica + +Melica ciliata L. +Enthaelt + +: +Melica ciliata L. subsp. ciliata + + + +Bestimmungsschluessel + + + +Zusammenfassung + + + + +Artbeschreibung + +(nach +Lauber & al. 2018 +) + +: +30-70 cm +hoch. +Blaetter +2-3 mm +breit, +/- +graugruen +, meist eingerollt, ohne Kiel. +Blatthaeutchen +1,5- +5 mm +lang, zerschlitzt. Blattscheiden kahl. + +Bluetenstand +eine dichte, zylindrische, +aehrige +Rispe + +, +6-15 cm +lang, aufrecht, zuletzt einseitswendig. +Aeste +kurz, unter den +Aehrchen +kurzhaarig. +Aehrchen +5-8 mm +lang, bleich, mit nur einer fertilen +Bluete +. Untere +Huellspelze +wenig +kuerzer +als die obere. + +Deckspelzen mit +2-3 mm +langen, gerade abstehenden Haaren + +. + + + + +Bluetezeit + +(nach +Lauber & al. 2018 +) + +: 5-7 + + +Standort und Verbreitung in der Schweiz + +(nach +Lauber & al. 2018 +) + +: Felsen, steinige +Haenge +in warmen Lagen, auf Kalk / kollin-montan(-subalpin) / J, A, M am Alpen- und Jurarand + + + + +Verbreitung global + +(nach +Lauber & al. 2018 +) + +: Mediterran + + + + +Oekologische +Zeigerwerte + +(nach +Landolt & al. 2010 +) + +1 + w42-44 + 4.h.2n=18 + + + +Status + + + +Status IUCN +: Nicht +gefaehrdet + + + +Anatomie + +Zusammenfassung +der Blattanatomie Obere Epidermiszellen gleich gross wie untere. Epidermiszellen aussen verholzt. Verbindungs-Steg zwischen oberer und unterer Epidermis aus verholzten und nicht verholzten Zellen. +Leitbuendel +im Verbindungs-Steg in der Mitte eingebettet. +Leitbuendelhuelle +ve + + +Zusammenfassung der Stammanatomie + + +Umriss rund mit Rippen. +Leitbuendel +in einer Reihe. Konische +Stuetzen +. Epidermiszellen verholzt. Chlorenchyma in peripheren runden, ovalen oder rechteckigen Gruppen. + + +Beschreibung (Englisch) + + +Culm-diameter +0.5-1 mm +, wall very large, radius of culm in relation to wall thickness approximately 1:0.75. Outline circular wavy. Culm-center hollow and surrounded by a few thin-walled, not lignified cells. Epidermis-cells thick-walled all around. Large vascular bundles arranged in one peripheral row. Chlorenchyma absent. Sclerenchyma in a large, peripheral continuous belt (> 3 cells). Cells thick-walled. Girders square, rectangular or conic. Small sclerenchymatic sheath with 1-2 cells around vascular bundles. Largest vessels in vascular bundles in lateral position. Largest vessel in the bundle small, <20μm. + + + +Oekologie + + + +Lebensform +Mehrjaehriger +Hemikryptophyt + + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + + + + + +
+4.1.1 - +Waermeliebende +Kalkfels-Pionierflur ( +Alysso-Sedion +) +
+
+ + +fett + +Dominante Art, welche das Aussehen des Lebensraumes +mitpraegt + +Charakterart +Weniger strikt an den Lebensraum gebundene Art + + +
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +trocken; Feuchtigkeit +maessig +wechselnd ( ++/- +1-2 Stufen) +Lichtzahl LhellSalzzeichen--
Reaktionszahl Rneutral bis basisch (pH 5.5-8.5)Temperaturzahl Twarm-kollin
+Naehrstoffzahl +N + +naehrstoffarm + +Kontinentalitaetszahl +K +subkontinental (niedrige relative Luftfeuchtigkeit, grosse Temperaturschwankungen, eher kalte Winter)
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Melica ciliata +L. + + + + + + +Volksname Deutscher Name: +Wimper-Perlgras +, +Gewimpertes Perlgras +Nom +francais +: + +Melique +ciliee + +Nome italiano: + +Melica barbata + + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Melica ciliata L. + + +Checklist 2017 + +256800
= +Melica ciliata L. + + +Flora Helvetica 2001 + +2677
= +Melica ciliata L. + + +Flora Helvetica 2012 + +2853
= +Melica ciliata L. + + +Flora Helvetica 2018 + +2853
= +Melica ciliata L. + + +Index synonymique 1996 + +256800
= +Melica ciliata L. + + +Landolt 1977 + +232
= +Melica ciliata L. + + +Landolt 1991 + +213
= +Melica ciliata L. + + +SISF/ISFS 2 + +256800
= +Melica ciliata L. + + +Welten & Sutter 1982 + +2242
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Status Indigenat +: Indigen + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein + + +Status Rote Liste national 2016 + + +Status IUCN +: Nicht +gefaehrdet + + + +Zusaetzliche +Informationen + +Kriterien IUCN: -- + + +Status Rote Liste regional 2019 + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Biogeografische RegionenStatusKriterien IUCN
Jura (JU) +nicht +gefaehrdet +(Least Concern) +
Mittelland (MP)verletzlich (Vulnerable)A3c
Alpennordflanke (NA) +nicht +gefaehrdet +(Least Concern) +
+Alpensuedflanke +(SA) + +nicht +gefaehrdet +(Least Concern) +
+Oestliche +Zentralalpen (EA) + +nicht +gefaehrdet +(Least Concern) +
Westliche Zentralalpen (WA) +nicht +gefaehrdet +(Least Concern) +
+
+ + +Status nationale +Prioritaet +/Verantwortung + + + + + + + +
+Keine nationale +Prioritaet +oder internationale Verantwortung +
+
+ +Schutzstatus + + + + + + +
Kein internationaler, nationaler oder kantonaler Schutz
+
+
+
+
\ No newline at end of file diff --git a/data/38/5C/61/385C611D235E5B0D9B1E4E54164EA1B9.xml b/data/38/5C/61/385C611D235E5B0D9B1E4E54164EA1B9.xml new file mode 100644 index 00000000000..af15e835ace --- /dev/null +++ b/data/38/5C/61/385C611D235E5B0D9B1E4E54164EA1B9.xml @@ -0,0 +1,477 @@ + + + +Two new species of cave-adapted pseudoscorpions (Pseudoscorpiones, Chthoniidae) from Yunnan, China + + + +Author + +Hou, Yanmeng +https://orcid.org/0000-0003-0059-3419 +The Key Laboratory of Zoological Systematics and Application, Institute of Life Science and Green Development, Hebei University, Baoding, Hebei 071002, China + + + +Author + +Gao, Zhizhong +https://orcid.org/0000-0002-6666-8746 +Department of Biology, Xinzhou Teachers University, Xinzhou 034000, Shanxi Province, China +gaozhizhong1987@126.com + + + +Author + +Zhang, Feng +https://orcid.org/0000-0002-3347-1031 +The Key Laboratory of Zoological Systematics and Application, Institute of Life Science and Green Development, Hebei University, Baoding, Hebei 071002, China +dudu06042001@163.com + +text + + +ZooKeys + + +2022 + +2022-04-20 + + +1097 + + +65 +83 + + + + +http://dx.doi.org/10.3897/zookeys.1097.82527 + +journal article +http://dx.doi.org/10.3897/zookeys.1097.82527 +1313-2970-1097-65 +6FC8EE30904F4E8D9EF9996F81F30693 +8FCFCC1D8266501EA79AAE732D44FF0B + + + + +Tyrannochthonius pandus +sp. nov. + + + + + +Chinese name. +弯指暴伪蝎 +Figs 2 + +, 3 +, 4 +, 5 + + + +Type material. + +(Figs +1A +, +6 +) +Holotype +: China • ♂; Yunnan Province, Luxi County, Luyuandong Village, the Ancient Alu Cave National Park of China, Biyu Cave; +24°34.01'N +, +103°45.16'E +; 1722 m a.s.l.; 13 Oct. 2021; Zegang Feng, Yanmeng Hou, Lu Zhang and Liu Fu leg.; dark zone; Ps.- +MHBU +-HBUARA#2021-438-01. +Paratype +: • 1♀; the same data as the holotype; Ps.- +MSWU +-HBUARA#2021-438-02. + + + +Figure 1. +Study area, general cave locations, and type locality for each species, Yunnan Province, China +A +Biyu Cave, + +Tyrannochthonius pandus + +sp. nov. +B +Laoxueyan Cave, + +Lagynochthonius laoxueyanensis + +sp. nov. + + + + +Diagnosis. +Moderately sized troglomorphic species with elongate appendages; carapace without eyes or eyespots; anterior margin of carapace gently serrate, epistome small, pointed, triangular, with 2 setae flanking base; posterior margin of carapace with 2 setae; tergites I-III with 2 setae; lacking chemosensory setae on dorsum of chelal hand; chelal fingers distinctly curved in dorsal view, with numerous large, gently curved, well-spaced teeth. + + +Etymology. + +The specific name is derived from the Latin word " +pandus +", meaning curved, refers to the curved chelal finger. + + + +Description. + +Adult male +(Figs +2 +, +3A +, +4A-D +, +5 +). +Color +: generally pale yellow, chelicerae, pedipalps and tergites slightly darker, soft parts pale (Figs +2 +, +3A +). +Cephalothorax +(Figs +4B +, +5A +): carapace 1.07 times longer than broad, gently narrowed posteriorly, surface smooth; anterior margin slightly serrate; without any traces of eyes; epistome very pointed and small, triangular, with 2 setae flanking base; with 18 setae arranged s4s: 4: 4: 2: 2, most setae heavy, long and gently curved, anterolateral setae much shorter than others; without furrows but with 4 lyrifissures (Fig. +5A +). Chaetotaxy of coxae: P 3, I 3, II 4, III 5, IV 5; manducatory process with two acuminate distal setae, anterior seta less than 1/2 length of medial seta; apex of coxa I with small, rounded anteromedial process; coxae II with 10 terminally indented coxal spines on each side, set as an oblique row, longer spines present in the middle of the row, becoming shorter distally and proximally and incised for about half their length (Fig. +5C +); intercoxal tubercle absent; without sub-oral seta. +Chelicera +(Figs +4C +, +5B +): large, about as long as carapace, 2.44 times longer than broad; 5 setae on hand, all setae acuminate, ventrobasal seta shorter than others; movable finger with one medial seta. Cheliceral palm with moderate hispid granulation dorsally. Both fingers well provided with teeth, fixed finger with 11 teeth, distal one largest; movable finger with 8 retrorse continuous small teeth; galea completely vestigial (Fig. +5B +). Rallum with 8 blades, the distal one longest and recumbent basally, with fine barbules and slightly set apart from the other blades, latter tightly grouped and with long pinnae, some of which are subdivided (Fig. +5D +). +Pedipalp +(Figs +4A +, +5E-H +): surface of palpal segments smooth; setae generally long and acuminate; femur 7.36, patella 2.55, chela 7.47, hand 2.80 times longer than deep; movable finger 1.71 times longer than hand and 0.64 times longer than chela, without large basal apodeme, only slightly sclerotized section present. Femur and dorsal hand without tactile setae but with 1 distal lyrifissure on patella (Fig. +5E +). Fixed chelal finger and hand with 8 trichobothria, movable chelal finger with 4 trichobothria, +ib +and +isb +situated close together, submedially on dorsum of chelal hand; +eb +, +esb +and +ist +forming a straight oblique row at base of fixed chelal finger; +it +slightly distal to +est +, situated subdistally; +et +slightly near to tip of fixed finger, very close to chelal teeth; +dx +situated distal to +et +; +sb +situated closer to +st +than to +b +; +b +and +t +situated subdistally, +b +situated at same level as +est +; +t +situated distal to +est +(Fig. +5F +). Microsetae (chemosensory setae) absent on hand and both chelal fingers. Sensilla absent. A tiny antiaxial lyrifissure present at base of fixed finger (slightly distal to +ist +). Both chelal fingers with a row of teeth, homodentate, spaced regularly along the margin, larger teeth present in the middle of the row, becoming smaller distally and proximally: fixed finger with 45 large, gently curved, well-spaced teeth, without intercalary teeth; movable finger with 44 small (slightly smaller than the teeth on fixed finger), retrorse, gently curved and well-spaced teeth (Fig. +5F +). Chelal fingers distinctly curved in dorsal view (Fig. +5H +). +Opisthosoma +: generally typical; pleural membrane finely granulate. Tergites and sternites undivided; setae uniseriate and acuminate. Tergal chaetotaxy I-XII: 2: 2: 2: 3: 4: 4: 4: 5: 5: 4: T2T: 0; tergites VIII and IX each with an unpaired median seta. Sternal chaetotaxy IV-XII: 10: 10: 9: 9: 9: 9: 8: 0: 2; sternites VI-IX with unpaired median seta. Anterior genital operculum with 10 setae, genital opening slit-like, with 15 marginal setae on each side (Fig. +4D +). +Legs +(Fig. +5I, J +): generally typical, long and slender. Femur of leg I 1.92 times longer than patella and with 1 lyrifissure at the base of femur; tarsus 2.50 times longer than tibia. Femoropatella of leg IV 3.67 times longer than deep; tibia 6.29 times longer than deep; with basal tactile setae on both tarsal segments: basitarsus 4.00 times longer than deep (TS = 0.35), telotarsus 14.50 times longer than deep and 2.90 times longer than basitarsus (TS = 0.33). Setae of leg I (trochanter to tibia) 3: 13: 12: 9, setae of leg IV (trochanter to basitarsus) 1: 3: 6: 9: 8. Arolium slightly shorter than the claws, not divided; claws simple. +Dimensions of male holotype +(length/width or, in the case of the legs, length/depth in mm; ratios in parentheses). Body length 1.41. Pedipalps: trochanter 0.18/0.13 (1.38), femur 0.81/0.11 (7.36), patella 0.28/0.11 (2.55), chela 1.12/0.15 (7.47), hand length 0.42/0.15 (2.80), movable finger length 0.72. Chelicera 0.44/0.18 (2.44), movable finger length 0.24. Carapace 0.45/0.42 (1.07). Leg I: trochanter 0.13/0.11 (1.18), femur 0.46/0.06 (7.67), patella 0.24/0.05 (4.80), tibia 0.20/0.04 (5.00), tarsus 0.50/0.04 (12.50). Leg IV: trochanter 0.20/0.11 (1.82), femoropatella 0.66/0.18 (3.67), tibia 0.44/0.07 (6.29), basitarsus 0.20/0.05 (4.00), telotarsus 0.58/0.04 (14.50). + + + +Figure 2. + +Tyrannochthonius pandus + +sp. nov., male habitus. Photographed when it crawled on stony natural habitat. + + + +Adult female +(Figs +3B +, +4E +). Mostly same as males. Anterior genital operculum with 10 setae plus 7 setae on posterior margin. Body length 1.67. Pedipalps: trochanter 0.24/0.13 (1.85), femur 0.88/0.13 (6.77), patella 0.28/0.11 (2.55), chela 1.20/0.17 (7.06), hand length 0.49/0.17 (2.88), movable finger length 0.76. Chelicera 0.45/0.21 (2.14), movable finger length 0.23. Carapace 0.46/0.46 (1.00). Leg I: trochanter 0.14/0.11 (1.27), femur 0.50/0.06 (8.33), patella 0.26/0.06 (4.33), tibia 0.21/0.05 (4.20), tarsus 0.53/0.04 (13.25). Leg IV: trochanter 0.21/0.12 (1.75), femoropatella 0.70/0.19 (3.68), tibia 0.46/0.07 (6.57), basitarsus 0.21/0.06 (3.50), telotarsus 0.62/0.04 (15.50). + + + +Figure 3. + +Tyrannochthonius pandus + +sp. nov. +A +holotype male, dorsal view +B +paratype female, dorsal view. Scale bars: 0.5 mm. + + + + +Figure 4. + +Tyrannochthonius pandus + +sp. nov., holotype male ( +A-D +), paratype female ( +E +) +A +chelal fingers (lateral view) +B +carapace (dorsal view) +C +left chelicera (dorsal view) +D +male genital area (ventral view) +E +female genital area (ventral view). Scale bars: 0.1 mm. + + + + +Remarks. + +Compared with the other six cave-dwelling species of the genus in China, + +Tyrannochthonius pandus + +sp. nov. is most similar to + +T. ganshuanensis + +in having only 2 setae on tergites I-III, the same chaetotaxy of carapace and triangular, a small epistome, but differs in the shape of teeth on chelal fingers (large, gently curved, well-spaced teeth, without intercalary teeth in + +T. pandus + +, but with pointed, well-spaced and intercalary teeth in + +T. ganshuanensis + +), the relative position of the trichobothria on the movable chelal finger ( +sb +situated closer to +st +than to +b +in + +T. pandus + +, but +sb +situated closer to +b +in + +T. ganshuanensis + +). + +Tyrannochthonius pandus + +sp. nov. can be easily separated from + +T. akaleus + +by a smaller body size (1.67 vs. 2.10 mm in female), the teeth pattern on chelal fingers (intercalary teeth absent in + +T. pandus + +, but present in + +T. akaleus + +); from + +T. harveyi + +by the different setae number on the anterior and posterior margins of the carapace ( + +T. pandus + +with 6 and 2 setae, respectively, but + +T. harveyi + +with 4 and 4 setae, respectively), the shape of the epistome (long and pointed in + +T. pandus + +, but rounded and inconspicuous in + +T. harveyi + +), the number of rallar blades (8 in + +T. pandus + +, but 6 in + +T. harveyi + +); and from + +T. zhai + +, + +T. chixingi + +and + +T. antridraconis + +by the number of setae on the anterior tergites (tergites I-III with 2 setae in + +T. pandus + +, but the other three with 4 setae). In addition, compared to the new species, + +T. zhai + +differs by the shorter body length (1.40 vs. 1.67 mm in female) and lacking an epistome; + +T. chixingi + +and + +T. antridraconis + +differs from the new species also by the presence of intercalary teeth on the fixed chelal finger ( +Mahnert 2009 +; +Gao et al. 2018 +; +Gao et al. 2020 +). + + + +Figure 5. + +Tyrannochthonius pandus + +sp. nov., holotype male +A +carapace (dorsal view) with a detail of anterior margin +B +left chelicera (dorsal view) with details of teeth +C +coxal spines on coxae II (ventral view) +D +rallum +E +left pedipalp (minus chela, dorsal view) +F +left chela (lateral view) with details of teeth and with trichobothrial pattern (abbreviations explained in Material and methods) +G +finger tips of chela (lateral view) +H +left chela (dorsal view) +I +leg I (lateral view) +J +leg IV (lateral view). Scale bars: 0.25 mm ( +A-B, E-F, H-J +); 0.10 mm ( +C-D, G +). + + + + +Distribution. + +This species is known only from the type locality, Biyu Cave (Figs +1A +, +6 +). Biyu Cave is one of the tourist caves in the Ancient Alu Cave National Park of China, with the entrance located in the Jilong hillside. This beautiful cave is a valley type karst cave, with an internal height of 2 to 5 m and a width of 1 to 30 m. The cave has a latticed distribution. The stalactites in this cave are jasper colored, so it is called Biyu Cave (a quote from the +cave's +interior slogan). The specimens of this new species were collected from under a stone and on a stone wall in an undeveloped area of the cave that is still in a natural condition. It is a small, dark, high humidity and low temperature space (temperature: 11 °C, humidity: 90%), which is suitable for the survival of the species. + + + +Figure 6. +Biyu Cave, type locality of + +Tyrannochthonius pandus + +sp. nov. +A +entrance +B +access to an undeveloped area +C +area where + +T. pandus + +specimens were collected. +D, E +beautiful cave landscapes inside the cave +F +exit. + + + + + \ No newline at end of file diff --git a/data/38/5C/87/385C87CC4C34FFACFF20FF720CE2FEC7.xml b/data/38/5C/87/385C87CC4C34FFACFF20FF720CE2FEC7.xml new file mode 100644 index 00000000000..bd8fbb4ee53 --- /dev/null +++ b/data/38/5C/87/385C87CC4C34FFACFF20FF720CE2FEC7.xml @@ -0,0 +1,269 @@ + + + +Myrmicella, a new genus of Harpactorinae (Hemiptera: Heteroptera: Reduviidae) from Madagascar + + + +Author + +Chłond, Dominik + + + +Author + +Baňař, Petr + +text + + +Zootaxa + + +2013 + +3718 + + +5 + + +483 +495 + + + +journal article +10.11646/zootaxa.3718.5.5 +7211df9b-e39f-4c42-9bed-07753284e855 +1175-5326 +218916 +679D97E8-0CAB-4950-8B10-A20960BE3632 + + + + + + + +Myrmicella verticospinosa + +sp. nov. + + + + +( +Figs 1–43 +) + + + + +Material examined. +Holotype +, male: ‘ZOM/ +Jan.2013/12 + +MADAGASCAR +/ ZOMBITSE N.P.; Andalabiby, + +771m +/ +S22°52’58.0‘‘ +E44°42’06.3‘‘ +; +26.i.2013 +/ +sifting litter; Winkler app. extr.; L.S. +/ +Rahanitriniaina & E.M. Rabotoson lgt. // +HOLOTYPE +/ + +Myrmicella verticospinosa + +/ gen. et sp. nov. / D. Chłond & P. Baňař det. 2013 + +(MMBC). +Paratypes +: +1 male +: ISL/ +Jan.2013/02 + +MADAGASCAR +/ ISALO N.P., Analalava forest + +; +719m +/ +S22°35’11.4‘‘ +E45°07’49.1‘‘ +; +17.i.2013 +/ +sifting litter; Winkler app. extr.; L.S. +/ +Rahanitriniaina & E.M. Rabotoson lgt. // +PARATYPE +/ + +Myrmicella verticospinosa + +/ gen. et sp. nov. / D. Chłond & P. Baňař det. 2013’ (MMBC); +1 female +: ‘ZOM/ +Jan.2013 +/YPT + +MADAGASCAR +/ ZOMBITSE N.P.; + +816m +, +26.i.2013 +/ +S22°53’11.4‘‘ +E44°41’31.8‘‘ +; +/ +YPT; L.S. Rahanitriniaina / & E.M. Rabotoson lgt. // +PARATYPE +/ + +Myrmicella verticospinosa + +/ gen. et sp. nov. / D. Chłond & P. Baňař det. 2013’, right fore, middle and hind legs mounted separately, specimen gold-plated for SEM study, genitalia not dissected (MMBC); +1 female +: ISL/ +Jan.2013/04 + +MADAGASCAR +/ ISALO N.P., Analalava forest + +; +725m +/ +S22°35’05.0‘‘ +E45°07’51.8‘‘ +; +17.i.2013 +/ +sifting litter; Winkler app. extr.; L.S. +/ +Rahanitriniaina & E.M. Rabotoson lgt. // +PARATYPE +/ + +Myrmicella verticospinosa + +/ gen. et sp. nov. / D. Chłond & P. Baňař det. 2013’ (MMBC). + + + + +Description. +Color. Body generally dark brown (females black to dark brown) with pale parts of connexiva, antenna, posterolateral parts of posterior lobe of pronotum, and wings (optically indicating narrowing of thorax ( +Figs 1–4 +)). Setae on all body faces pale. Head dark brown (with black postocular part and dark brown area between ocelli in females). First and second visible segments of labium dark brown, second visible segment with paler apical part, third visible segment pale. Labrum brown. Eyes black (dark brown with black central facets and paler marginal facets in females). Scapus, pedicellus, and basiflagellomere brown, distiflagellomere with brown basal half and yellowish apical half. Anterior lobe of pronotum dark brown, darker laterally. Posterior pronotal lobe black with pale lateral margins and medial part. Thorax dark brown with black markings. Hemelytra pale, scutellum brown. Coxae brown with black markings. Trochanters dark brown, pale basally and apically. Femora dark brown with distinctly darker basal part. Tibiae brown, tarsi light brown. Abdominal tergites brown with black posterior part (black with irregular dark brown markings medially and laterally, as well as abdominal tergite VII with distinctly paler lateral parts in females). Connexiva bicolorous—black with yellowish posterior part. Ventral side of abdomen black (with paler medial part of sternites III–V in females). Pygophore black. + +Structure. Head fusiform with flattened ventral side in lateral view. Postocular part of head 1.18 times as long as anteocular part and distinctly higher laterally. Eyes large, globular, slightly elongated vertically with flattened posterior margin in lateral view. Ocelli not pigmented. Setae on scapus scarce, short, and suberected. Pedicellus and basiflagellomere covered by dense, short, erected and suberected setae. Setation on distiflagellomere very dense, various sized, adherent, and erected. Pair of trichobothria on clypeus, gula, and basal part of first visible labial segment. First visible labial segment enlarged apically. Second labial segment slightly enlarged medially. Third visible segment short and wide. All labial segments with scarce, very short and erected setae and distinctly longer trichobothria. First visible labial almost reaching posterior margin of eyes. Pronotum covered mostly by scarce, short, erected setae. Distinctly developed collar covered medially by white, short, and flat setae. Spines on lateral parts of collar distinctly enlarged in basal part. Anterior pronotal lobe enlarged, distinctly gibbous with very distinct and deeply depressed line posteriorly. Posterior pronotal lobe with distinct sculpture (visible mostly posteriorly) and with distinctly visible punctuation interiorly (near transversal suture) and laterally. Transversal suture wide with distinct punctuation. Scutellum with vertical and very long, rounded apex. Vertical part of scutellum with wide basal part and slightly curved margins. Horizontal part of scutellum shiny with distinctly visible lateral sculptures (convex and curved lines). Reduced hemelytra distinctly curved and covered by pale, short, dense, and suberected setae. Femora covered by sparse, long, erected setae. Tibia with dense various sized, erected setae and very dense, short adherent setae. Abdomen ovoid in dorsal view with dull medial part of tergites. Lateral parts of tergites with distinct sculpturing. Middle part of posterior margin of each tergite curved (tergites 3– 5 curved distinctly towards dorsal abdominal glands). Sternites dull with small shiny spots and delicate sculpture laterally. Abdomen, pygophore, and parameres covered by sparse, various sized, erected setae. + +Male genitalia. Genital capsule as in +Figs 35–36 +, elongate, with regular rows of long, erected to semierected setae directed posteriorly. Apical part with two symmetrical, hook-like processes. Posterolateral margins of genital capsule covered with a row of straight setae, directed posteriorly. Paramere ( +Figs 37–38 +) long, narrow, regularly rounded apically, on dorsolateral surface densely covered with long, erected setae. Articulatory apparatus of phallus long and thin ( +Fig. 41 +). Phallus ventrally with weakly sclerotized membrane, overlapping non-inflated phallus in its whole length; dorsally with paired dorsal phallothecal sclerite ( +Figs 39–40 +), reaching proximal twothirds of phallus. Endosoma very complicated, showing strongly different details in inflated and uninflated phallus, with conspicuously three-dimensional, variously shaped, sclerotized, and denticulate structures. Some such structures show ventralmost ( +Fig. 42 +) and inner ( +Fig. 43 +) part of endosoma. Missing left dorsal sclerotized plate ( +Fig. 40 +) showing sclerotized structures from dorsal view. + + +Female genitalia. Valvifer 1 subtriangular with robust setae on outer surface and elongated, revolute apex ( +Fig. 30 +). Valvula 1 thin and elongated, sickle-curved with wider apical part ( +Fig 30 +). Valvula 2 and valvifer 2 thin and elongated (together x-shaped) ( +Fig. 29 +). Valvula 3 with two pairs of erected and robust setae ( +Fig. 28 +). + + +Measurements +(in mm), male +holotype +(female +paratypes +in parentheses). +Total body length +—5.55 (5.92– 5.95). +Head. +Total length (without neck)—1.25 (1.11–1.31); diatone-0.93 (0.83–0.84) dorsal synthlipsis (minimum interocular distance)—0.45 (0.39–0.44); length of anteocular part: 0.50 (0.43–0.44); length of postocular part— 0.50 (0.51–0.53); +Labium +. Total length—1.65 (1.42–1.51); segment I, length—0.80 (0.62–0.75); segment II, length—0.65 (0.53–0.60); segment III, length—0.20 (0.20–0.23). +Antenna +. Segment I, length—1.40 (1.56–1.60); segment II, length—1.05 (0.93–0.95); segment III, length—1.05 (0.95–1.04); segment IV, length—1.25 (1.13– 1.24). +Pronotum +. Total length (maximum)—1.26 (1.02–1.21); anterior lobe maximum length—0.81 (0.76–0.74); posterior lobe, maximum length—0.45 (0.45–0.44); anterior lobe, width (maximum)—0.90 (0.87–0.88); posterior lobe, width (maximum)—1.05 (0.98–1.03). +Scutellum +. Total length (maximum)—0.23 (0.33–0.33). +Forewing +. Maximum length—0.33 (0.30–0.43). +Maximum width of abdomen +: 1.52 (1.85–1.88). + + + + +FIGURE 44. +Distibution of + +Myrmicella verticospinosa + +gen +. et +sp. nov. +in Madagascar. + + + + +Etymology. +The name of this species is connected with the vertical scutellar spine. + + +Habitat and collecting method. +All specimens of + +Myrmicella verticospinosa + +were collected in semideciduous forests with a canopy height up to + +10 m +. + +Three specimens were sifted using a sieve and subsequent extraction in Winkler apparatus. A single female was collected (although micropterous) in the yellow pan trap in the forest. + + + + +Distribution. +South-west +Madagascar +, Zombitse-Vohibasia National Park and Isalo National Park ( +Fig. 44 +). + + + + \ No newline at end of file diff --git a/data/38/5C/A1/385CA13089AC54579C2CA8E6A0EEBDD5.xml b/data/38/5C/A1/385CA13089AC54579C2CA8E6A0EEBDD5.xml new file mode 100644 index 00000000000..6ab61a5cc2e --- /dev/null +++ b/data/38/5C/A1/385CA13089AC54579C2CA8E6A0EEBDD5.xml @@ -0,0 +1,138 @@ + + + +Genus-level revision of the Alycaeidae (Gastropoda, Cyclophoroidea), with an annotated species catalogue + + + +Author + +Pall-Gergely, Barna +Plant Protection Institute, Centre for Agricultural Research, Herman Otto ut 15, Budapest, H- 1022, Hungary +https://orcid.org/0000-0002-6167-7221 +pallgergely2@gmail.com + + + +Author + +Sajan, Sheikh +Zoological Survey of India, Prani Vigyan Bhawan, M Block, New Alipore, Kolkata 700053, West Bengal, India & Wildlife Institute of India, Chandrabani, Dehradun 248 002, Uttarakhand, India +https://orcid.org/0000-0002-2785-6824 + + + +Author + +Tripathy, Basudev +Zoological Survey of India, Prani Vigyan Bhawan, M Block, New Alipore, Kolkata 700053, West Bengal, India + + + +Author + +Meng, Kaibaryer +National Zoological Museum of China, Institute of Zoology, Chinese Academy of Sciences, Beijing, China + + + +Author + +Asami, Takahiro +Department of Biology, Shinshu University, Matsumoto 390 - 8621, Japan +https://orcid.org/0000-0001-5706-0272 + + + +Author + +Ablett, Jonathan D. +Mollusca Section, Invertebrates Division, Department of Life Sciences, The Natural History Museums, London SW 7 5 BD, United Kingdom + +text + + +ZooKeys + + +2020 + +981 + + +1 +220 + + + + +http://dx.doi.org/10.3897/zookeys.981.53583 + +journal article +http://dx.doi.org/10.3897/zookeys.981.53583 +1313-2970-981-1 +5194AAC86B8A473F8A41470A60182A0B +7C44C797C4125A71BAE032A55E6FA5DC + + + + + +Stomacosmethis altispirus ( +Moellendorff +, 1902) + + + + + +Alycaeus perakensis altispirus +Moellendorff +, 1902: 144-145. + + +Alycaeus (Alycaeus) perakensis altispirus +- +Zilch 1957 +: 147, pl. 6, fig. 32. + + +Alycaeus altispirus +- +Foon and Liew 2017 +: 21-23, figs 7A, B, 10, 31A. + + + +Type locality. + +"Kelantan, +Ostkueste +der Halbinsel Malacca" (from the title). + + + +Material examined. + +Malakka, Kelantan, coll. +Moellendorff +, SMF 109738 (lectotype, designated by +Zilch 1957 +). + + + +Remarks. +Protoconch very finely granulated, without spiral lines; R1 with irregular, low ribs and very weak spiral striation in-between, approximately same strength; R2 very short, with darker thick and fewer than ten lighter narrower stripes very slightly elevated from the surface. + +This taxon was described as a subspecies of + +A. perakensis + +. We agree with +Foon and Liew (2017) +that it should be handled as a species due to the characteristic flat whorls and expanded peristome. + + + + \ No newline at end of file diff --git a/data/38/5D/23/385D23F2B1E9274E877C4F6AA9DC7932.xml b/data/38/5D/23/385D23F2B1E9274E877C4F6AA9DC7932.xml new file mode 100644 index 00000000000..0d463b65913 --- /dev/null +++ b/data/38/5D/23/385D23F2B1E9274E877C4F6AA9DC7932.xml @@ -0,0 +1,125 @@ + + + +Revision of the Australian species of the weevil genus Trigonopterus Fauvel + + + +Author + +Riedel, Alexander + + + +Author + +Taenzler, Rene + +text + + +ZooKeys + + +2016 + +556 + + +97 +162 + + + + +http://dx.doi.org/10.3897/zookeys.556.6126 + +journal article +http://dx.doi.org/10.3897/zookeys.556.6126 +1313-2970-556-97 +FFA73BF51AA34BF085B81C44F838B040 +FFA73BF51AA34BF085B81C44F838B040 + + + + +Taxon +classification Animalia Coleoptera Curculionidae + + + + +10. +Trigonopterus cooktownensis Riedel +sp. n. + + + +Diagnostic description. +Holotype (Fig. 10a). Length 2.95 mm. Color black. Body subovate, almost without constriction between pronotum and elytron; in profile evenly convex. Rostrum with median costa and pair of submedian costae dorsally flattened; intervening furrows with rows of silvery scales; apical 1/3 rugose-punctate. Eyes with dorsal margin bordered by furrow. Forehead with sparse coarse punctures. Pronotum with disk punctate; sides with punctures slightly larger; interspaces not microreticulate; base slightly extended towards elytral suture. Elytra with striae marked by rows of minute punctures; along base and humeri with row of large punctures; apex with dense rows of small shallow punctures. Legs. Femora microreticulate, punctate. Metafemur dorsally with elongate patch of dense silvery scales; posterior surface with pair of longitudinal furrows containing rows of scales parallel to ventral and dorsal edge; dorsoposterior edge indistinct. Mesotibia apically with uncus and premucro largely fused, with shallow incision at apex. Metatibia apically with uncus and distinct premucro. Abdominal ventrite 2 swollen, with posterior edge projecting, medially forming common cavity with ventrite 1; ventrite 5 concave, dull, microreticulate, punctate. Penis (Fig. 9b) with sides of body subparallel, weakly converging; apex with median triangular extension confluent with outline of apex; transfer apparatus short, dentiform, apically bordered by pair of L-shaped sclerites; ductus ejaculatorius without bulbus. + + +Figure 10. +Trigonopterus cooktownensis +sp. n., holotype; a Habitus b Penis. + + + + + +Material +examined. + + +Holotype (QMBA): ARC3698 (EMBL # LN888183), Queensland, Cooktown, Mt. Cook N.P., +S15°28.648' +, +E145°15.793' +, to +S15°29.252' +, +E145°15.992' +, 63-245 m, 23-IV-2014. Paratypes (ANIC, SMNK): Queensland: 1 ex, Cooktown, Mt. Cook N.P., +S15°29' +, +E145°16' +, 11-12-X-1980; 1 ex, Cooktown, Mt. Cook N.P., +S15°28.648' +, +E145°15.793' +, to +S15°29.252' +, +E145°15.992' +, 63-324 m, 24-IV-2014. + + + +Distribution. +Queensland (Mt. Cook). + + +Biology. + +Beaten from foliage of +Acacia +-dominated forest. + + + +Etymology. +This epithet is an adjective based on the name of the type locality, Cooktown. + + +Notes. + +Trigonopterus cooktownensis +Riedel, sp. n. was coded as " +Trigonopterus +sp. 566". It occurs syntopically with +Trigonopterus albidosparsus +Lea. + + + + \ No newline at end of file diff --git a/data/38/5D/87/385D879491592C6D89D5A8F0FA63F87E.xml b/data/38/5D/87/385D879491592C6D89D5A8F0FA63F87E.xml new file mode 100644 index 00000000000..3405ec192d0 --- /dev/null +++ b/data/38/5D/87/385D879491592C6D89D5A8F0FA63F87E.xml @@ -0,0 +1,196 @@ + + + +Brachyopa minima (Diptera: Syrphidae), a new species from Greece with notes on the biodiversity and conservation of the genus Brachyopa Meigen in the Northern Aegean Islands + + + +Author + +Pérez-Bañón, Celeste + + + +Author + +Radenković, Snezana + + + +Author + +Vujić, Ante + + + +Author + +Ståhls, Gunilla + + + +Author + +Rojo, Santos + + + +Author + +Grković, Ana + + + +Author + +Petanidou, Theodora + +text + + +Zootaxa + + +2016 + +4072 + + +2 + + +217 +234 + + + +journal article +46869 +10.11646/zootaxa.4072.2.5 +e2074875-e2a7-4912-8291-67ac248be3a0 +1175-5326 +270665 +557C6E0E-5A87-4E52-8DCE-5D47CB13AE1E + + + + + + +Key to the members of the + +Brachyopa quadrimaculosa + +species group in the Eastern Mediterranean + + + + +(following +Doczkal & Dziock 2004 +) + + + + + + +1. Scutellum entirely covered in microtrichia................................. + +Brachyopa bimaculosa +Doczkal & Dziock + + + + +- Scutellum largely bare of microtrichia, at least on posterior 1/2–1/3.............................................. 2 + + + + + +2. Proepimeron with a few pile anteriorly. Scutum with rounded bare spots at the transverse suture ( +Figs 3 +C & D)........... 3 + + + +- Proepimeron bare. Scutum with microtrichose transverse suture................................................. 5 + + + + + +3. Lateral sides of scutum uniformly covered with light grey microtrichia....... + +Brachyopa vernalis + +van Steenis & van Steenis + + + + +- Lateral sides of scutum with stripes of dark grey microtrichia... (as in +Fig. 3 +C)..................................... 4 + + + + + + +4. Postalar callus with a very small bare spot ( +Fig. 3 +C); male terminalia illustrated in +Kaplan & Thompson (1981: 209, Figs 16– 18) +............................................... + +Brachyopa quadrimaculosa +Thompson + +in Kaplan & Thompson + + + + +- Postalar callus with large bare spot (see van Steenis & van Steenis 2004: +Fig. 4 +).................................................................................................. + +Brachyopa cruriscutum + +van Steenis & van Steenis + + + + + + +5. Sensory pit present; scutum with bare spots and stripes ( +Figs 3 +A & B); tergites with pale pile; male terminalia in +Figs 4–5 +.................................................................................. + +Brachyopa minima + + +sp. nov. + + + + + +- Sensory pit absent; scutum completely microtrichose except for the postalar callus; second tergite with black pile posteromedi- ally in female (can be absent in male); (male terminalia illustrated in Vujić (1991: 147, +Fig. 4 +B)....................................................................................................... + +Brachyopa insensilis +Collin + + + + + + + \ No newline at end of file diff --git a/data/38/5D/87/385D8794915A2C6E89D5AB38FD7CF81C.xml b/data/38/5D/87/385D8794915A2C6E89D5AB38FD7CF81C.xml new file mode 100644 index 00000000000..3326528f882 --- /dev/null +++ b/data/38/5D/87/385D8794915A2C6E89D5AB38FD7CF81C.xml @@ -0,0 +1,155 @@ + + + +Brachyopa minima (Diptera: Syrphidae), a new species from Greece with notes on the biodiversity and conservation of the genus Brachyopa Meigen in the Northern Aegean Islands + + + +Author + +Pérez-Bañón, Celeste + + + +Author + +Radenković, Snezana + + + +Author + +Vujić, Ante + + + +Author + +Ståhls, Gunilla + + + +Author + +Rojo, Santos + + + +Author + +Grković, Ana + + + +Author + +Petanidou, Theodora + +text + + +Zootaxa + + +2016 + +4072 + + +2 + + +217 +234 + + + +journal article +46869 +10.11646/zootaxa.4072.2.5 +e2074875-e2a7-4912-8291-67ac248be3a0 +1175-5326 +270665 +557C6E0E-5A87-4E52-8DCE-5D47CB13AE1E + + + + + + + +Brachyopa quadrimaculosa + +group sensu +Kassebeer (2002) + + + + +Based on adult characteristics, both species belong to the + +B. quadrimaculosa + +group sensu +Kassebeer (2002) +. The members of this species group share the following adult morphological characters: length of pile on arista shorter than maximum width of arista; ground colour of scutum entirely black (with exceptions of the postalar callus); postpedicellus without distinct sensory pit (if a pit is present its diameter is smaller than the maximum diameter of the arista). + + +Considering all available data, the following species belong to the + +Brachyopa quadrimaculosa + +group: + +B. atlantea + +, + +B. cinerea +Wahlberg + +, + +B. bimaculosa +Doczkal & Dziock + +, + +B. cruriscutum + +van Steenis & van Steenis, + +B. grunewaldensis +Kassebeer + +, + +B. insensilis + +, + +B. quadrimaculosa + +, + +B. primorica +, +B. silvae + +Doczkal & Dziock, + +B. stackelbergi + +, + +B. tabarkensis + +and + +B. vernalis + +. + + + + \ No newline at end of file diff --git a/data/38/5D/87/385D8794915A2C6E89D5AE85FD76FA32.xml b/data/38/5D/87/385D8794915A2C6E89D5AE85FD76FA32.xml new file mode 100644 index 00000000000..63500222314 --- /dev/null +++ b/data/38/5D/87/385D8794915A2C6E89D5AE85FD76FA32.xml @@ -0,0 +1,169 @@ + + + +Brachyopa minima (Diptera: Syrphidae), a new species from Greece with notes on the biodiversity and conservation of the genus Brachyopa Meigen in the Northern Aegean Islands + + + +Author + +Pérez-Bañón, Celeste + + + +Author + +Radenković, Snezana + + + +Author + +Vujić, Ante + + + +Author + +Ståhls, Gunilla + + + +Author + +Rojo, Santos + + + +Author + +Grković, Ana + + + +Author + +Petanidou, Theodora + +text + + +Zootaxa + + +2016 + +4072 + + +2 + + +217 +234 + + + +journal article +46869 +10.11646/zootaxa.4072.2.5 +e2074875-e2a7-4912-8291-67ac248be3a0 +1175-5326 +270665 +557C6E0E-5A87-4E52-8DCE-5D47CB13AE1E + + + + + + + +Brachyopa quadrimaculosa +Thompson + +in Kaplan & Thompson + + + + + + +Material studied. +Greece +, Lesvos, Agiassos, Sanatorio, 0 1.05.2008, +1 male +, leg. Vujić; +Greece +, Samos, Manolates (on + +Smyrnium + +sp.), +17.04.2011 +, +12 males +(G0302, G0303 ( +DNA +voucher specimen +FSUNS +–Y1447_J–001), G0305, G0307–G0309, G0311–G0313, G0315, G0316), +2 females +(G0304 = +DNA +voucher specimen +FSUNS +– Y1448_J–002, G0314), leg. Vujić and Radenković; Samos, Pyrgos, +15.04.2011 +, +1 male +(G0317), leg. Vujić and Radenković; (all in +FSUNS +). + + + + +Comments. +The species was originally described from +Israel +( +Kaplan & Thompson 1981 +) and first recorded for Europe by +Speight (2013) +, who cites it from Evros province in North Eastern +Greece +(M. De Courcy, pers. comm.). Later, van Steenis & van +Steenis (2014) +published a record of a taxon related to + +B. quadrimaculosa + +from Samos Island based on one female. They indicated that this taxon differs morphologically from + +B. vernalis + +van Steenis & van Steenis and + +B. quadrimaculosa + +. After studying a +paratype +of + +B. quadrimaculosa + +(male, +Israel +, Mongort, +4 March 1976 +, leg. A. Friedberg & M. Kaplan, coll. +TAU +), it can be confirmed that this specimen does not belong to an undescribed species but is conspecific with + +B. quadrimaculosa + +. The diagnostic characters of this species are presented in the key (see below). + + + + \ No newline at end of file diff --git a/data/38/5D/87/385D8794915C2C6E89D5ABADFE88FCD0.xml b/data/38/5D/87/385D8794915C2C6E89D5ABADFE88FCD0.xml new file mode 100644 index 00000000000..461cd4c7c15 --- /dev/null +++ b/data/38/5D/87/385D8794915C2C6E89D5ABADFE88FCD0.xml @@ -0,0 +1,251 @@ + + + +Brachyopa minima (Diptera: Syrphidae), a new species from Greece with notes on the biodiversity and conservation of the genus Brachyopa Meigen in the Northern Aegean Islands + + + +Author + +Pérez-Bañón, Celeste + + + +Author + +Radenković, Snezana + + + +Author + +Vujić, Ante + + + +Author + +Ståhls, Gunilla + + + +Author + +Rojo, Santos + + + +Author + +Grković, Ana + + + +Author + +Petanidou, Theodora + +text + + +Zootaxa + + +2016 + +4072 + + +2 + + +217 +234 + + + +journal article +46869 +10.11646/zootaxa.4072.2.5 +e2074875-e2a7-4912-8291-67ac248be3a0 +1175-5326 +270665 +557C6E0E-5A87-4E52-8DCE-5D47CB13AE1E + + + + + + + +Brachyopa minima +Vujić & Pérez-Bañón + +sp. nov. + + + + + + +Diagnosis. +Small species ( +6–7 mm +). Scutum ( +Figs 3 +A, B) covered with grey microtrichia except: pair of small bare spots posteromedian to the postpronotum; a pair of large bare spots anterior to transverse suture and median to notopleural sulcus; spots at the median ends of transverse sulcus covered by brown microtrichia; postalar callus with a bare spot; two stripes bare of microtrichia on posterior part of scutum located laterally. Male terminalia on +Figs 4–5 +; surstylus with well-developed ventral lobe ( +Figs 4 +A, 5 A); dorsal and ventral margins of surstylus straight ( +Figs 4 +A, 5 A); hypandrium wide with complex apical appendages ( +Figs 5 +C, D). + + + + + +Type +material. + +HOLOTYPE +: +Greece +, Lesvos, Karini, +13.04.2011 +, +1 male +(G0322), leg. Vujić (in +FSUNS +). +PARATYPES +: +Greece +, Lesvos, Karini, +13.04.2011 +, +4 males +(G018–G020, G023), +1 female +(G0324), +13.04.2013 +, +1 female +(G2805), leg. Vujić (in +FSUNS +); +30.04.2008 +, +1 male +(G3069), leg. Vujić (in +FSUNS +); +Greece +, Lesvos, Karini, +26.04.2007 +, +1 male +(G3068) +1 female +(G3067), leg. Pérez-Bañón and Vujić (in +FSUNS +). +Greece +, Lesvos, Karini, 3.05.2007, leg. Pérez-Bañón, +1 female +, +DNA +voucher specimen +MZH +_Y544 (in +MZH +). + + + + +Etymology. +The specific epithet + +minima + +means "smallest" and refers to the size of the species, which is smaller than most other members of the genus. + + + + +FIGURE 2. +SEMs of head features of male + +Brachyopa minima + + +sp. nov. +A: + +face; +B: +orbital strip; +C: +antenna; +D: +scutellum. + + + + +Description. MALE. +Body length +6–7 mm +, wing length +7 mm +. +Head +( +Figs 1 +A, C; 2 A–C). Length to height ratio of head 0.97. Face moderately protruding ( +Fig. 1 +C). Length to width ratio of clypeus 1.4. Length to width ratio of subcranial cavity 1.6; 1.7 times as wide as the shortest distance from the eye to the subcranial cavity. Orbital strip ( +Figs 2 +A, B) shallow, in narrower part as wide as the maximum width of arista. Pile on all parts of the head capsule pale, except black pile on upper part of occiput near eye margin. Frons and vertex ( +Fig. 1 +A) microtrichose, only narrow area above lunule and around ocelli bare. Length of eye contiguity about 0.4 times the length of frons, shorter than ocellar triangle. Distance between posterior ocellus and eye margin about equal to two ommatidium diameters. Hypostomal bridge grey-reddish, paler anteriorly, entirely microtrichose, except bare hypostomal sulcus. Face ( +Figs 2 +A, B) microtrichose except for a fascia from the tentorial sulcus to the mouth. Length to height ratio of postpedicellus 1–1.15, with small sensory pit ( +Fig. 2 +C). Arista ( +Fig. 2 +C) with very short pile (shorter than 1/3 the maximum width of arista), with orange base and darkened toward apex. +Thorax. +Black except for the postalar callus, which is partly reddish, and the metasternum and probasisternum which are more or less reddish. Scutum ( +Figs 3 +A, B) entirely densely covered in grey microtrichia except for a pair of bare maculae posteromedian to the postpronotum; a pair of bare maculae anterior to transverse suture and median to notopleural sulcus (maculae at the median ends of transverse sulcus covered by brown microtrichia); postalar callus with a bare spot; two stripes bare of microtrichia on posterior part of scutum located laterally. Notopleural sulcus impressed. Thoracic bristles not well differentiated from the pile. Postpronotum pale haired, with few black pile mixed in. + + +Scutum predominantly black haired except for its anterior margin and the notopleuron, which are pale haired, a few pale pile that are present at the supra-alar area, and the postalar callus that is pale haired. Scutellum rather trapezoidal, without a distinct depression, mainly orange, only slightly darkened anteriorly and anterolaterally, with two pairs of strong black marginal bristles; predominantly pale haired mixed with black pile medially; only anterior half covered with microtrichia ( +Fig. 2 +D). Mediotergite microtrichose below subscutellum, except at posterior margin. Proepimeron and anterior flat part of mesanepisternum bare. Posterior surface of mid coxa without pile. Legs orange, 5th tarsomere of all legs black, tarsomeres 1–4 of metatarsus darkened dorsally. Legs pale pilose except for the usual black bristles on hind femur ventrally, apex of mesotibia ventrally with strong black bristles, the ventral surface of mesotarsus with black bristles. Haltere yellow with light yellow capitulum. Wing without dark spots. +Abdomen. +Tergites and sternites orange, except first tergite and first sternite with dark grey area laterally, pile all pale. First tergite entirely microtrichose, second tergite extensively covered with microtrichia except for the posterior margin narrowly and large area at the posterolateral corners, which are bare. Sternites entirely densely microtrichose. Male terminalia on +Figs 4–5 +. +FEMALE. +Differs from the male in the following characters: length to width ratio of frons 1.46–1.54. Frons ( +Fig. 1 +B) entirely microtrichose except shiny anterior area above antennae, with small central microtrichose spot (this spot lacking in + +B. quadrimaculosa + +). A narrow pollinose stripe running from the dusted area of the frons downward along the eye margin, widening beside the lunule and merging with the wide pollinose cross band that covers the dorsal part of face (face less covered by microtrichia than in male, without bare spot below each antenna, contrary to + +B. quadrimaculosa + +) ( +Fig. 1 +B). Length to height ratio of postpedicellus 1.14–1.15, a little larger than in male, with a minute sensory pit. Tibiae and tarsi darker than in male. + + + + \ No newline at end of file diff --git a/data/38/5D/87/385D87B7FFA2F87A2D94FF25FAAEFC78.xml b/data/38/5D/87/385D87B7FFA2F87A2D94FF25FAAEFC78.xml new file mode 100644 index 00000000000..5fca2fba62f --- /dev/null +++ b/data/38/5D/87/385D87B7FFA2F87A2D94FF25FAAEFC78.xml @@ -0,0 +1,865 @@ + + + +Taxonomy of Petrosiidae Van Soest, 1980 (Haplosclerida, Porifera) from Brazil + + + +Author + +Rocha, Lívia +0000-0002-5284-1309 +liviahrocha @ yahoo. com. br; https: // orcid. org / 0000 - 0002 - 5284 - 1309 +liviahrocha@yahoo.com.br + + + +Author + +Moraes, Fernando +0000-0001-8251-6868 +fmoraes @ mn. ufrj. br; https: // orcid. org / 0000 - 0001 - 8251 - 6868 +fmoraes@mn.ufrj.br + + + +Author + +Salani, Sula +0000-0003-3850-1030 +Laboratório de Bentos, Instituto de Ciências Biológicas, Universidade de Brasília. Campus Universitário Darcy Ribeiro, Bloco E, s / n, Asa Norte, CEP 70910 - 900, Brasília / DF, Brazil. & sulasm @ gmail. com; https: // orcid. org / 0000 - 0003 - 3850 - 1030 +sulasm@gmail.com + + + +Author + +Hajdu, Eduardo +0000-0002-8760-9403 +eduardo. hajdu @ gmail. com; https: // orcid. org / 0000 - 0002 - 8760 - 9403 +eduardo.hajdu@gmail.com + +text + + +Zootaxa + + +2021 + +2021-07-20 + + +5004 + + +2 + + +251 +287 + + + +journal article +10.11646/zootaxa.5004.2.2 +1175-5326 +5677189 +B1B2F144-2B51-4079-ACB5-6D78B38B32E7 + + + + + + + +Petrosia +( +Petrosia +) +weinbergi +Van Soest, 1980 + + + + + + + +( +Fig. 1 +, +3 +; +Tab. 3 +, +5 +) + + + + + + + +Petrosia weinbergi +, +Van Soest 1981: 21 + + +; + +Alcolado & Gotera 1986: 2 + +; + + +Hajdu +et al +. 2011: 96 + + +; + +Alcolado & Busutil 2012: 71 + +. + + +Petrosia +( +Petrosia +) +weinbergi +, +Moraes 2011: 185 + + +; + + +Rützler +et al +. 2014: 90 + + +; + +Van Soest 2017: 37 + +. + + + +Additional synonymy in + +Muricy +et al +. 2011: 106 + +. + + + + + +Studied material ( +23 specimens +): + + +Brazil +, +Rio Grande do Norte State +, +Atoll das Rocas +: +MNRJ 2917 +, +Salãozinho Tide Pool +( +3.87559º S +, +33.80881º W +), + +3 m +depth + +, +Col. F. Moraes +, + +1999.7.4 + +; +MNRJ 2942 +, Deep Fenda crevice ( +3.85000º S +, +33.78333º W +), + +5 m +depth + +, +Col. F. Moraes +, + +1999.12.6 + +; +MNRJ 6387 +, +6388 +, +6389 +, +6390 +, +dos Mapas Tide Pool +( +3.86945º S +, +33.81797º W +), + +2 m +depth + +, +Col. E. Hajdu, M +. Ventura & +U. Pinheiro +, + +2002.8.28 + +; +MNRJ 6682 +, +6683 +, +6852 +, Deep Fenda crevice ( +3.85000º S +, +33.78333º W +), + +5 m +depth + +, +Col. E. Hajdu, M +. Ventura & +U. Pinheiro +, + +2002.8.25 + +. +Pernambuco State +: +MNRJ 7843 +, + +Buraco +da Raquel + +( +3.83446º S +, +32.39733º W +, +Fernando de Noronha Archipelago +), + +2 m +depth + +, +Col. F. Moraes +, + +2003.11.10 + +; +MNRJ 8615 +, Cordilheira ( +3.85000º S +, +32.41667º W +, +Fernando de Noronha Archipelago +), + +20 m +depth + +, +Col. F. Moraes +, + +2004.8.10 + +; UFRJPOR 3916 ( +Fernando de Noronha Archipelago +), +Col. G. Muricy +, + +1996.03.01 + +; UFRJPOR 4046, Biquara Reef ( +8.75000º S +, +35.10000º W +, Tamandaré), depth not recorded, +Col. G. Muricy +, + +1996.3.9 + +. +Bahia State +: +MNRJ 2602 +, West side of quebra-mar, +Capitania dos Portos +( +12.96361º S +, +38.51556º W +, +Port Authority +breakwater, Salvador), + +15–20 m +depth + +, +Col. E. Hajdu +, + +1999.8.7 + +; +MNRJ 2643 +, South side of quebra-mar, +Capitania dos Portos +( +12.96361º S +, +38.51556º W +, +Port Authority +breakwater, +Salvador +), + +15–20 m +depth + +, +Col. E. Hajdu +, + +1999.8.7 + +; +MNRJ 8311 +, +between Farol da Barra and Porto da Barra +, depth not recorded, +Col. E. Hajdu +, + +2004.06.03 + +; +MNRJ 10588 +, South side of quebra-mar, +Capitania dos Portos +( +12.96361º S +, +38.51556º W +, +Port Authority +breakwater, Salvador), + +5.8 m +depth + +, +Col. E. Hajdu +, + +2007.12.14 + +; +MNRJ 11120 +, Cantagalo beach, ‘Blackadder’ Shipwreck ( +12.93517º S +, +38.51181º W +, +Salvador +), + +7.9 m +depth + +, +Col. E. Hajdu +& +G. Harfush +, + +2009.5.31 + +; +MNRJ 21014 +, +Pedra de Leste +, +Parcel das Paredes +( +17.80000º S +, +38.91667º W +, Caravelas, Abrolhos Bank), + +6 m +depth + +, +Col. F. Moraes +, + +2016.5.5 + +; +MNRJ 18141 +, +Recife das Timbebas +(ca. +17.39635º S +, +39.02636º W +), + +10 m +depth + +, +Col. F. Moraes +, + +2014.2.23 + +; UFRJPOR 4723, +Parcel das Paredes +(ca. +17.76280º S +, +38.98045º W +), +Col. G. Muricy +, + +1997.10.31 + +. off Espírito Santo State, +Trindade Island +: +MNRJ 7396 +, +Ponta dos Farrilhões +( +20.51667º S +, +29.31667º W +), + +28 m +depth + +, +Col. G. Muricy +, + +2003.8.18 + +; +MNRJ 7402 + +, + +Ilha +Sul +, + +12 m +depth + +, +Col. G. Muricy +& +F. Moraes +, + +2003.8.18 + + +. + + +External morphology. +Thickly encrusting to massive, up to +20 cm +wide. Uneven surface. Oscules rounded ( +1–4 mm +diam.), dispersed at the surface level or slightly elevated (volcaniform), showing lighter color edges. Microhispid texture. Consistency hard and friable. Color +in vivo +varying from olive-green, with or without red-wine tinges, yellowish-brown, white or beige ( +Fig. 3A +). + + + + +Skeleton. +Ectosomal, detachable, with scarce spongin, showing a tangential anisotropic reticulation, where stout primary tracts formed by oxeas I and II surround irregular polygonal meshes (415–580 μm wide) of pauci- to multispicular tracts (95–195 μm thick). Thinner, secondary to tertiary tracts, also formed by oxeas I and II, delimit smaller irregular polygonal meshes (50–240 μm wide), formed by uni- to paucispicular tracts (15–100 μm thick). Oxeas III are found along the spicule tracts, single or in bundles, varying in density among specimens ( +Fig. 3B–C +). Some specimens ( +e.g. +MNRJ 6388) showed a nearly isotropic ectosomal reticulation of paucispicular tracts, with considerably reduced numbers of oxeas III attached to these tracts. Choanosomal, a loose lamellate-isotropic reticulation with rounded meshes (145–630 μm wide), formed by multispicular tracts (50–165 μm thick) in variably welldefined layers parallel to the surface. Rounded or elongated canals (100–1,100 μm wide) are commom between these parallel tracts ( +Fig. 3C +). Dispersed, slender oxeas I and II confer a disorganized aspect to the choanosome, these being rare in the ectosome. Single rare oxeas III are also found dispersed in the choanosome. + + +Spicules +( +Table 3 +). Oxeas in three size classes. Oxeas I ( +Fig. 3F, I +), larger, smooth, slightly curved, with mucronate, rounded, conic, hastate and acerate ends 194–229 (16.6)–334/ 5–9 (2.4)– +15 µm +. Oxeas II ( +Fig. 3G, J +), intermediate, resembling the former, but smaller 63–109 (27.4)–189/ 5–7 (2.1)– +15 µm +. Oxeas III ( +Fig. 3H, K +), smaller, smooth, straight to slightly curved, with conic, mucronate and hastate ends, 19–37 (8.6) 59/ 5–5 (0.7) +15 µm +. Specimens Oxea (length/ width) + + + +FIGURE 3. + +Petrosia +( +Petrosia +) +weinbergi +van Soest, 1980 + +. +In situ +image of specimen (A) MNRJ 11120, (B–C) tangential section and morphological variation of the ectosomal architecture, (D–E) perpendicular sections through the choanosome, (F) oxeas I, (G) oxeas II, (H) oxeas III, (I) details of the apices of oxeas I, (J) details of the apices of oxeas II, (K) details of the apices of oxeas III. B, D, F–K, MNRJ 10588; C, E, MNRJ 6388. Scale bars, (A) 1 cm, (B–E) 100 µm, (F–K) 10 µm. + + + + +TABLE 3. +Spicule measurements of + +Petrosia +( +Petrosia +) +weinbergi +Van Soest, 1980 + +. Values given as min.-–med. (SD)– max, in µm. + + +Atoll das Rocas + +MNRJ +2917 I +: 194–215 (19)–242/ 10–9 (0.6)–15 + +II: 63–107 (24.3)–189/ 5–7 (2.3)–10 +III: 24–34 (9.9)–58/ 5–6 (1.7) 10 + +MNRJ +2942 I +: 194–210 (14)–252/ 5–9.3 (1.7)–15 + +II: 63–123 (36.7)–189/ 5–8 (2.4)–10 +III: 24–37 (14.8)–53/ 5–5 (0)–5 +MNRJ 6387 I: 194–224 (13.2)–252/ 5–7 (2.4)–10 +II: 63–114 (31.4)–189/ 5–5 (0.7)–10 +III: 19–30 (8)–53/ 5–5 (0)–5 +MNRJ 6388 I: 194–226 (17.5)–257/ 5–8 (2.4)–10 +II: 73–106 (24.4)–174/ 5–7 (2.4)–10 +III: 24–36 (12.8)–58/ 5–5 (0)–5 +MNRJ 6389 I: 194–212 (11.3)–232/ 5–6 (1.9)–10 +II: 68–121 (37.4)–189/ 5–5 (1)–10 +III: 24–34 (5.7)–44/ 5–5 (1.1)–10 +MNRJ 6390 I: 194–216 (26.6)–261/ 5–7 (2.4)–10 +II: 63–108 (31.3)–179/ 5–5 (0)–5 +III: 19–30 (9.9)–58/ 5–5 (0)–5 +MNRJ 6682 I: 194–227 (14.9)–257/ 5–9 (2)–15 +II: 63–103 (25.6)–184/ 5–6 (2.5)–15 +III: 24–34 (9.5)–58/ 5–5 (1.1)–10 +MNRJ 6683 I: 194–221 (20.9)–252/ 5–7 (2.5)–10 +II: 63–103 (25.3)–160/ 5–5 (0)–5 +III: 24–33 (7.4)–48/ 5–5 (0)–5 +MNRJ 6852 I: 194–235 (14.6)–266/ 5–9 (2)–15 +II: 63–107 (32.6)–184/ 5–6 (1.9)–10 +III: 19–36 (9.8)–48/ 5–5 (0)–5 + + +Pernambuco +, + +Fernando +de Noronha + + + + + +MNRJ 7843 + +I: 194–233 (15.1)–266/ 5–8 (2.7)–15 + +II: 68–103 (18.9)–145/ 5–7 (2.4)–10 +III: 24–33 (12)–58/ 5–5 (0)–5 +MNRJ 8615 I: 194–236 (19.3)–266/ 5–9 (2.1)–15 +II: 63–103 (27.4)–189/ 5–6 (2.3)–10 +III: 29–41 (10.6)–58/ 5–5 (0)–5 +UFRJPOR 3916 I: 208–253 (15.6)–290/ 5–7 (2.4)–10 +II: 68–112 (23.3)–155/ 5–5 (0.8)–5 +III: 29–38 (6.4)–48/ 5–5 (0)–5 + +Pernambuco +, Tamandaré + +URRJPOR 4046 I: 194–207 (12.5)–232/ 5–7 (3.3)–15 +II: 63–98 (21.2)–145/ 5–7 (2.4)–10 +III: 24–31 (6.1)–48/ 5–5 (0)–5 + +Bahia + +UFRJPOR 4723 I: 194–27 (21.6)–334/ 10–14 (1.1)–15 +II: 68–113 (31.3)–179/ 10–12 (2.4)–15 +III: 29–42 (8.4)–59/ 5–7 (2.5)–10 + +......continued on the next page + + + + +TABLE 3. (Continued) + +Specimens +MNRJ 2602 + + + +Ecology. + +Petrosia +( +P. +) +weinbergi + +specimens here studied were recorded from several habitats, including coastal reefs, bays, and volcanic, as well as biogenic (atoll) oceanic islands, at +2–28 m +depth, which fits its previously known depth range ( +1.5–184 m +depth; +Zea 1987 +; + +Campos +et al +. 2005 + +). One specimen agglutinated debris (MNRJ 2602) and another was found over polychaete tubes and cirripeds (MNRJ 11120). + + + + +Distribution. +Tropical Atlantic. +Brazil +: +Maranhão State +( + +Campos +et al +. 2005 + +); +Rio Grande do Norte State +( + +Muricy +et al. +2008 + +); +Pernambuco State +( +Muricy & Moraes 1998 +); +Bahia State +( + +Hajdu +et al +. 2011 + +); off +Espírito Santo State +(Trindade Island) ( + +Moraes +et al. +2006 + +; +Moraes 2011 +). Caribbean ( +Van Soest 1980 +, +1981 +; +Pulitzer-Finali 1986 +; +Zea 1987 +; +Lehnert & Van Soest 1998 +; +Díaz 2005 +; +Alcolado & Busutil 2012 +; + +Rützler +et al +. 2000 + +, +2014 +). +Suriname +( +Van Soest 2017 +). + + + + +Remarks. +The specimens of + +Petrosia +( +P. +) +weinbergi + +studied here, including those reported upon by +Moraes (2011) +and + +Hajdu +et al +. (2011) + +, which were reanalysed, resemble the original description of the species, including massive morphology, occasional green color +in vivo +, rounded oscules ( +2–5 mm +wide) scattered on the surface, reticulated ectosome and choanosome, and a smaller category of oxeas concentrated in the ectosome ( +Van Soest 1980 +; see +Table 5 +below). Morphological and anatomical similarities were also observed in the studied specimens when compared to the redescriptions by +Zea (1987) +, + +Campos +et al +. (2005) + +, + +Rützler +et al +. (2014) + +and +Van Soest (2017 +; see +Table 5 +below). The tubular external morphology observed by +Pulitzer-Finali (1986) +in the material from La Parguera ( +Puerto Rico +) differentiates it from the specimens studied here, but the skeletal architecture, and the three size categories of oxeas are shared characters. Despite the obvious anatomical specialization of the smallest category of oxeas, we decided to double check the number of categories through aplication of the Sturges Algorithm ( +Sturges 1926 +). Our bar graphs (not shown) clearly point to the existence of three size categories of oxeas. This is in contrast to +Alcolado & Gotera (1986) +, who did not separate size classes of oxeas in their study, but mentioned instead that there was a wide size variation, and the resemblance of the smallest oxeas to microxeas. +Pulitzer-Finali (1986) +reported specimens with wide variation in a single category of oxeas ( +Puerto Rico +), and others with three, more clearly distinguishable categories ( +Puerto Rico +and +Dominican Republic +). +Zea (1987) +, on the other hand, mentioned only two size categories of oxeas, highlighting the presence of a wide variation in their sizes. + + +We noticed a marked variation in the density of the ectosomal skeleton in Brazilian specimens, which varied from obviously anisotropic, including rather stout, to paucispicular or even unispicular tracts; to nearly isotropic, with no stout multispicular tracts. These lighter arrangements also implied considerably reduced numbers of oxeas III attached to the tracts. It is tempting to associate this dichotomy to the distance from sources of continental silica, Atoll das Rocas and the Fernando de Noronha Archipelago being over +250 km +offshore. Nevertheless, both skeletal arrangements are found in coastal, as well as in oceanic sites. For example, MNRJ 2917, 2942, 6387, 6390 and 6682 exhibit an anisotropic ectosome and came from Atoll das Rocas, while MNRJ 6388 and 6389, from the same locality, exhibit an isotropic arrangement. The same occurred in Fernando de Noronha Archipelago, with UFRJPOR 3916 and MNRJ 7843 being anisotropic, and MNRJ 8615, isotropic. In Bahia State ( +Salvador +City), again, specimens MNRJ 2643, 10588 and 11120 exhibit an anisotropic ectosomal architecture, while MNRJ 2602 and 8311 have an isotropic reticulation instead. Remarkably, this variation in skeletal density does not appear to be matched by a similar variation in spicule thickness. Both Fernando de Noronha and Bahia ( +Salvador +) showed equally thick spicules (up to +15 µm +) to be present in aniso-, as well as isotropic ectosomal skeletal arrangements. In Atoll das Rocas, specimens with isotropic arrangements appeared not to possess spicules thicker than +10 µm +(MNRJ 6388, 6389), while those with anisotropic arrangements had them similarly only as thick as +10 µm +(MNRJ 6387, 6390), or as thick as +15 µm +(MNRJ 2917, 2942, 6682). + +Petrosia +( +P. +) +weinbergi + +might benefit from an integrative taxonomic approach, to figure if there is any genetic diversity hidden underneath this apparent morphologic plasticity. + + + + \ No newline at end of file diff --git a/data/38/5D/87/385D87B7FFA4F8602D94FA14FD2DF849.xml b/data/38/5D/87/385D87B7FFA4F8602D94FA14FD2DF849.xml new file mode 100644 index 00000000000..887f4e70250 --- /dev/null +++ b/data/38/5D/87/385D87B7FFA4F8602D94FA14FD2DF849.xml @@ -0,0 +1,185 @@ + + + +Taxonomy of Petrosiidae Van Soest, 1980 (Haplosclerida, Porifera) from Brazil + + + +Author + +Rocha, Lívia +0000-0002-5284-1309 +liviahrocha @ yahoo. com. br; https: // orcid. org / 0000 - 0002 - 5284 - 1309 +liviahrocha@yahoo.com.br + + + +Author + +Moraes, Fernando +0000-0001-8251-6868 +fmoraes @ mn. ufrj. br; https: // orcid. org / 0000 - 0001 - 8251 - 6868 +fmoraes@mn.ufrj.br + + + +Author + +Salani, Sula +0000-0003-3850-1030 +Laboratório de Bentos, Instituto de Ciências Biológicas, Universidade de Brasília. Campus Universitário Darcy Ribeiro, Bloco E, s / n, Asa Norte, CEP 70910 - 900, Brasília / DF, Brazil. & sulasm @ gmail. com; https: // orcid. org / 0000 - 0003 - 3850 - 1030 +sulasm@gmail.com + + + +Author + +Hajdu, Eduardo +0000-0002-8760-9403 +eduardo. hajdu @ gmail. com; https: // orcid. org / 0000 - 0002 - 8760 - 9403 +eduardo.hajdu@gmail.com + +text + + +Zootaxa + + +2021 + +2021-07-20 + + +5004 + + +2 + + +251 +287 + + + +journal article +10.11646/zootaxa.5004.2.2 +1175-5326 +5677189 +B1B2F144-2B51-4079-ACB5-6D78B38B32E7 + + + + + + + +Neopetrosia subtriangularis +( +Duchassaing, 1850 +) + + + + + +Brazilian records +(not examined): + +Brazil +, +Maranhão State +, MCNPOR 5340, +0.36667º S +, +44.86667º W +, + +72 m +depth + +, Coll. +R +. +V +. ‘Antares’, + +2001.7.18 + + +; + +MCNPOR 5003, +0.58667º S +, +43.34861º W +, + +94 m +depth + +, Coll. +R +. +V +. ‘Antares’, + +1999.6.14 + + +. + + + + +Diagnosis. +Thick ramose fragments. Smooth surface, with conspicuous oscules, +1.5–6 mm +diam. Ectosome uni- to multispicular network, with triangular to polygonal meshes (80–280 μm in diam., tracts 10–90 μm thick). Choanosome with rectangular and triangular meshes (80–250 μm diam.), channels 200–440 μm diam., primary multispicular ascending tracts (up to 15 spicules across, 40–60 μm diam.), uni to plurispicular interconnecting sec- ondary tracts (20–70 μm thick). Oxeas, slightly curved, acerate, blunt to conical ends, simple or stepped, 60–230 x 2.5–6.9 μm [adapted from + +Campos +et al. +2005 + +]. + + + + +Description. +Refer to + +Campos +et al +. (2005) + +. + + + + +Distribution. +Tropical Atlantic. +Brazil +: +Maranhão State +( + +Campos +et al. +2005 + +); Caribbean ( +Van Soest 1980 +; +Zea 1987 +; +Lehnert 1993 +); +Suriname +( +Van Soest 2017 +). + + + + \ No newline at end of file diff --git a/data/38/5D/87/385D87B7FFA5F8612D94FD7EFC7BFA33.xml b/data/38/5D/87/385D87B7FFA5F8612D94FD7EFC7BFA33.xml new file mode 100644 index 00000000000..85b05c32bff --- /dev/null +++ b/data/38/5D/87/385D87B7FFA5F8612D94FD7EFC7BFA33.xml @@ -0,0 +1,396 @@ + + + +Taxonomy of Petrosiidae Van Soest, 1980 (Haplosclerida, Porifera) from Brazil + + + +Author + +Rocha, Lívia +0000-0002-5284-1309 +liviahrocha @ yahoo. com. br; https: // orcid. org / 0000 - 0002 - 5284 - 1309 +liviahrocha@yahoo.com.br + + + +Author + +Moraes, Fernando +0000-0001-8251-6868 +fmoraes @ mn. ufrj. br; https: // orcid. org / 0000 - 0001 - 8251 - 6868 +fmoraes@mn.ufrj.br + + + +Author + +Salani, Sula +0000-0003-3850-1030 +Laboratório de Bentos, Instituto de Ciências Biológicas, Universidade de Brasília. Campus Universitário Darcy Ribeiro, Bloco E, s / n, Asa Norte, CEP 70910 - 900, Brasília / DF, Brazil. & sulasm @ gmail. com; https: // orcid. org / 0000 - 0003 - 3850 - 1030 +sulasm@gmail.com + + + +Author + +Hajdu, Eduardo +0000-0002-8760-9403 +eduardo. hajdu @ gmail. com; https: // orcid. org / 0000 - 0002 - 8760 - 9403 +eduardo.hajdu@gmail.com + +text + + +Zootaxa + + +2021 + +2021-07-20 + + +5004 + + +2 + + +251 +287 + + + +journal article +10.11646/zootaxa.5004.2.2 +1175-5326 +5677189 +B1B2F144-2B51-4079-ACB5-6D78B38B32E7 + + + + + + + +Neopetrosia +aff. +carbonaria +( +Lamarck, 1814 +) + + + + + + + + + +Neopetrosia carbonaria +( +Lamarck, 1814 +) + +: + + +Muricy +et al +. 2011: 106 + + +(in part, only Brazilian records). + + + + + + +Studied material ( +14 specimens +): + + +Brazil +, +Ceará State + +, + +MNRJ 17400 +, +Acaraizinho de Amontada +, intertidal, +Col + +. + +R +. +Farias +and +K. Santiago Santiago +, 2013.11; +Trairí City +: +Mundaú +beach ( +3.17418º S +, +39.35723º W +) + +: + +MNRJ 17866 +, +1 +m depth, +Col. M. S. Carvalho +, + +2014.3.29 + + +; + +MNRJ 17741 +, +1 +m depth, +Col. E. Hajdu +, + +2014.3.29 + + +; + +MNRJ 17766 +, +1 +m depth, +Col. E. Hajdu +, + +2014.3.31 + + +; + +MNRJ 17777 +, +1 +m depth, +Col. A. Bispo +, + +2014.3.29 + + +; + +MNRJ 17832 +, +1 +m depth, +Col. S. Salani +, + +2014.3.29 + + +; + +Flecheiras Beach +( +3.21858º S +, +39.26344º W +) + +: + +MNRJ 17782 +, +1 +m depth, +Col. A. Bispo +, + +2014.3.30 + + +; + +MNRJ 17783 +, +1 +m depth, +Col. A. Bispo +, + +2014.3.30 + + +; + +MNRJ 17840 +, +1 +m depth, +Col. S. Salani +, + +2014.3.30 + + +; + +MNRJ 17887 +, +1 +m depth, +Col. M. S.Carvalho +, + +2014.3.30 + + +. + +Rio Grande do Norte State +, +MNRJ 18033 +, +Parrachos de Maracajaú +, +Maxaranguape City +( +5.40114º S +, +35.29677º W +), depth not record, +Col. S. Salani +, + +2014.4.6 + + +. + +Alagoas State +, +Maceió City +: +Ponta Verde Beach +( +9.65000º S +, +35.68333º W +) + +: + +MNRJ 4713 +, + +0.5–1 m +depth + +, +Col. E. Hajdu +, + +2001.9.3 + + +; + +Recife Ponta do Meirim +( +9.70000º S +, +35.76667º W +) + +: + +MNRJ 17035 +, + +0.5–1 m +depth + +, +Col. A. Bispo +, + +2012.1.10 + + +. + +Bahia State +: +MNRJ 18690 +, +Abrolhos Bank +, +Pedra de Leste +, + +3 m +depth + +, +Col. F. Moraes +, + +2014.6.30 + + +. + + +Comparative material. + +Spongia carbonaria +Lamarck, 1814 + +, +Holotype +MNHN-LBIM-DT 545, Schizotype +MNRJ +21834. + +Adocia carbonaria +, +Hechtel (1976) + +, +YPM +IZ +008960, +Pernambuco State +(Recife), digitized images of dissociated spicules and thick anatomical sections. + + + + +Remarks. +We found toxas in many Brazilian specimens studied (MNRJ 4713, 9405, 17034, 17400), hitherto unreported for the species, and seemingly absent from the +holotype +reexamined here. These toxas can be quite rare, and occur in both black or brown sponges. We consider Brazilian + +N. carbonaria + +-like sponges as likely belonging to a new species under description by Santos +et al. +(in prep., pers, comm.). For this reason, we preferred to withdraw its full description from our study to avoid overlapping their results. + + + + \ No newline at end of file diff --git a/data/38/5D/87/385D87B7FFA5F8612D94FF25FD46FD5B.xml b/data/38/5D/87/385D87B7FFA5F8612D94FF25FD46FD5B.xml new file mode 100644 index 00000000000..08ee88a5ac4 --- /dev/null +++ b/data/38/5D/87/385D87B7FFA5F8612D94FF25FD46FD5B.xml @@ -0,0 +1,169 @@ + + + +Taxonomy of Petrosiidae Van Soest, 1980 (Haplosclerida, Porifera) from Brazil + + + +Author + +Rocha, Lívia +0000-0002-5284-1309 +liviahrocha @ yahoo. com. br; https: // orcid. org / 0000 - 0002 - 5284 - 1309 +liviahrocha@yahoo.com.br + + + +Author + +Moraes, Fernando +0000-0001-8251-6868 +fmoraes @ mn. ufrj. br; https: // orcid. org / 0000 - 0001 - 8251 - 6868 +fmoraes@mn.ufrj.br + + + +Author + +Salani, Sula +0000-0003-3850-1030 +Laboratório de Bentos, Instituto de Ciências Biológicas, Universidade de Brasília. Campus Universitário Darcy Ribeiro, Bloco E, s / n, Asa Norte, CEP 70910 - 900, Brasília / DF, Brazil. & sulasm @ gmail. com; https: // orcid. org / 0000 - 0003 - 3850 - 1030 +sulasm@gmail.com + + + +Author + +Hajdu, Eduardo +0000-0002-8760-9403 +eduardo. hajdu @ gmail. com; https: // orcid. org / 0000 - 0002 - 8760 - 9403 +eduardo.hajdu@gmail.com + +text + + +Zootaxa + + +2021 + +2021-07-20 + + +5004 + + +2 + + +251 +287 + + + +journal article +10.11646/zootaxa.5004.2.2 +1175-5326 +5677189 +B1B2F144-2B51-4079-ACB5-6D78B38B32E7 + + + + + + + +Neopetrosia sulcata +Santos, Sandes, Cabral & Pinheiro, 2016 + + + + + + + + + +Holotype + +(not examined). +Brazil +, +Rio Grande do Norte State +, UFPEPOR 17, +Potiguar Basin +( +4.62547º S +, +36.76686º W +), + +70–101 m +depth + +, leg. +Petrobras +, + +2003.5.4 + +. + + + + + +Diagnosis. +Irregularly cylindrical fragments. Surface punctiform or furrowed, rugose to the touch, with scattered circular oscules ( +1.5–10 mm +diam.), always flush with the surface. Consistency hard, slightly brittle. Ectosome formed by tangential multispicular tracts (50–250 μm diam.), with rounded meshes (150–300 μm diam.), and the apical brushes of oxeas from longitudinal choanosomal spicule tracts. Choanosomal skeleton isotropic, with a superimposed anisotropic orientation of multispicular tracts and single spicules strewn in confusion. Oxeas smooth, relatively robust, usually curved, with fairly high percentage of variations at the ends (mucronate, stepped, hastate, asymmetrical, or blunt), 119–193 x 2.8– 9.6 μm [adapted from + +Santos +et al. +2016 + +]. + + + + +Description. +Refer to + +Santos +et al +. (2016) + +. + + + + +Distribution. +Tropical Atlantic. +Brazil +: +Maranhão State +( + +Campos +et al. +2005 + +, as + +N. proxima + +); Potiguar Basin, +Rio Grande do Norte State +( + +Santos +et al. +2016 + +). + + + + \ No newline at end of file diff --git a/data/38/5D/87/385D87B7FFADF8602D94FF25FABBFA88.xml b/data/38/5D/87/385D87B7FFADF8602D94FF25FABBFA88.xml new file mode 100644 index 00000000000..a163cbf243b --- /dev/null +++ b/data/38/5D/87/385D87B7FFADF8602D94FF25FABBFA88.xml @@ -0,0 +1,1518 @@ + + + +Taxonomy of Petrosiidae Van Soest, 1980 (Haplosclerida, Porifera) from Brazil + + + +Author + +Rocha, Lívia +0000-0002-5284-1309 +liviahrocha @ yahoo. com. br; https: // orcid. org / 0000 - 0002 - 5284 - 1309 +liviahrocha@yahoo.com.br + + + +Author + +Moraes, Fernando +0000-0001-8251-6868 +fmoraes @ mn. ufrj. br; https: // orcid. org / 0000 - 0001 - 8251 - 6868 +fmoraes@mn.ufrj.br + + + +Author + +Salani, Sula +0000-0003-3850-1030 +Laboratório de Bentos, Instituto de Ciências Biológicas, Universidade de Brasília. Campus Universitário Darcy Ribeiro, Bloco E, s / n, Asa Norte, CEP 70910 - 900, Brasília / DF, Brazil. & sulasm @ gmail. com; https: // orcid. org / 0000 - 0003 - 3850 - 1030 +sulasm@gmail.com + + + +Author + +Hajdu, Eduardo +0000-0002-8760-9403 +eduardo. hajdu @ gmail. com; https: // orcid. org / 0000 - 0002 - 8760 - 9403 +eduardo.hajdu@gmail.com + +text + + +Zootaxa + + +2021 + +2021-07-20 + + +5004 + + +2 + + +251 +287 + + + +journal article +10.11646/zootaxa.5004.2.2 +1175-5326 +5677189 +B1B2F144-2B51-4079-ACB5-6D78B38B32E7 + + + + + + + +Neopetrosia proxima +( +Duchassaing & Michelotti, 1864 +) + + + + + + + +( +Fig. 1 +, +2 +; +Tab. 1–2 +) + + + + + + + +Neopetrosia proxima +, + +Campos +et al +. 2005: 13 + + + +; + + +Muricy +et al +. 2011: 106 + + +; + + +Santos +et al +. 2016: 336 + + +; + + +Pérez +et al +. 2017: 10 + + +; + +Van Soest 2017: 35 + +; + + +Vicente +et al. +2019: 8 + + +, Fig. 9. + + + +Additional synonymy in + +Muricy +et al +. 2011: 106 + +. + + + + + +Studied material ( +15 specimens + +): + +Brazil +, +Amapá State + +, + +MNRJ 18737 +, off the +Amazon River +mouth ( +3.590445° N +, +49.126713° W +), + +90 m +depth + +, +Col. F. Moraes + +& + +R +. +Moura +/ NHo ‘ +Cruzeiro do Sul’ +, + +2014.9.26 + + +; + +UFRJPOR 933, +Amazon River +mouth ( +NOAS +Station +1773A), depth not recorded, +Col. C.E.Z. +/ NOc. ‘ +Almirante Saldanha’ +. +Bahia State +, +Salvador City + +: + +MNRJ 2516 +, ‘ +Blackadder’ Shipwreck +, +Cantagalo +beach ( +12.93517º S +, +38.51181º W +), depth not recorded, +Col. E. Hajdu +et al +., + +1999.8.3 + + +; + +MNRJ 2558 +, +2561 +, quebra-mar +Norte +( +12.96667º S +, +38.50000º W +, northern breakwater), depth not recorded, +Col. E. Hajdu +, +et al +., + +1999.8.1 + + +; + +MNRJ 2601 +, +2606 +, quebra-mar, +Capitania dos Portos +( +Port Authority +breakwater), SW location ( +12.65000º S +, +38.75000º W +), depth not recorded, +Col. M. Leblanc +, + +1999.8.6 + + +; + +MNRJ 2639 +, +Capitania dos Portos +( +Port Authority +), outer location ( +12.65000º S +, +8.75000º W +), depth not recorded, +Col. E. Hajdu +et al +., + +1999.8.7 + + +; + +MNRJ 10526 +, quebra-mar +Norte +( +12.96667º S +, +38.50000º W +, northern breakwater), + +5.3 m +depth + +, +Col. E. Hajdu +, + +2007.7.11 + + +; + +UFRJPOR 4160, +Ribeira +beach ( +12.91933º S +, +38.50215º W +), depth not recorded, +Col. P. Young +, + +1994.2.3 + + +; + +MNRJ 6016 +, +Off Salvador +, +Station + + +R4 +(REVIZEE/ +Central +SCORE +, +Campaign +6, +13.07500º S +, +38.39194º W +), + +91 m +depth + +, +Col. N +/ +Rb. +‘ +Astro Garoupa’ +, + +2002.6.23 + + +; + +Madre de Deus City + +: + +MNRJ 8375 +, +8419 +, +8427 +, +2 +nd +Boião +( +BL 2 +beacon signalling) ca. +4 km +off SW +Maré Isl. +( +12.818295º S +, +38.569177º W +), depth not recorded, +Col. E. Hajdu +& +C. Santos +, + +2004.6.7 + + +. + +MNRJ 5998 + +, + +Rio de Janeiro State +, +Station Y +2 ( +RE- VIZEE +/ Central-SCORE, +Campaign +6, +22.38222º S +, +37.58750º W +, +Almirante Saldanha Seamount +), + +250–500 m +depth + +, +Col. N +/ +Rb. +‘ +Astro Garoupa’ +, + +2002.6.12 + + +. + + +Comparative material. + +Thalysias proxima +Duchassaing & Michelotti, 1864 + +—Spicule and skeleton slides from the Schizolectotype deposited in the Natural History Museum (London), +BMNH +12.11.1928 +45a ( +Fig. 2A +). + + + +TABLE 1. +Spicule measurements of + +Neopetrosia proxima +( +Duchassaing & Michelotti, 1864 +) + +. Values given in min.–med. (SD)–max. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
SpecimensOxea (length/ width)
Schizolectotype, BMNH 12.11.1928 45a91–129 (18.4)–161/ 2–4 (1)–5 µm
Amapá
MNRJ 18737149–181 (15.6)–216/ 2–4 (2.1)–10 µm
UFRJPOR 933131–159 (12.2)–184/ 5–7 (2.3)–10 µm
Bahia
MNRJ 2516136–163 (11.5)–184/ 5–9 (1.7)–10 µm
MNRJ 2558102–149 (19.4)–179/ 5–8 (2.3)–10 µm
MNRJ 2561111–152 (14.1)–179/ 5–8 (2.3)–10 µm
MNRJ 2601131–164 (13.2)–189/ 5–9 (1.8)–10 µm
MNRJ 2606107–156 (22.9)–194/ 5–9 (2)–10 µm
MNRJ 2639116–155 (15.6)–189/ 5–7 (2.5)–10 µm
MNRJ 6016114–140 (11.8)–162/ 2–3 (0.6)–4 µm
MNRJ 8375116–154 (15.8)–174/ 5–8 (2.2)–10 µm
MNRJ 8419140–165 (11.1)–184/ 5–10 (1.8)–15 µm
MNRJ 8427121–158 (13.3)–184/ 5–9 (1.7)–10 µm
MNRJ 10526116–141 (11.4)–160/ 5–8 (2.4)–10 µm
UFRJPOR 416097–142 (18.7)–169/ 5–8 (2.4)–10 µm
Rio de Janeiro
MNRJ 5998123–148 (12.2)–171/ 2–3 (0.8)–5 µm
+
+ + +TABLE 2. +Comparative morphological data for + +Neopetrosia +spp. + +from the Western Tropical Atlantic. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Species +H. += habitus; +S. += surface; +Cv. += color +in vivo +; +Cs. += consistency; +O. += oscules; +E. += ectosome; +Ch. += choanosome; +n.o. += not ob- served; +n.r. += not reported + +Spicules + +Locality/ Depth +
+ + +N. carbonaria +( +Lamarck, 1814 +) + + +( +sensu +Topsent, 1930/1931) + +H. +with long fistules; +S. +uniform, soft; +Cv. +black; +Cs. +fragile, friable; +O. +n. o.; +E. +superposed triang. and squar. meshes; +Ch. +spongin-less multispic. tracts parallel to surface. + +Oxeas: I, +210–215/ 8–14 µm; +II, +165/ 4 µm +Caribbean/ n.r.
+Oxeas: +121–160/ 2.1–9.6 µm. +
+H. +thick crust with irreg. shape; +S. +Scatt., pointy conules, or smooth ridges; +Cv. +ext. reddish-brown to dark purple, int. light-yellow; +Cs. +
+ + +N. cristata +Vicente, Ríos, Zea & Toonen, 2019 + + +(orig. descr) + +firm, crumbly; +O. +aligned on ridges or on top of conical elevs, ˂1 mm diam.; +E. +with confused or loose multispic. tracts, forming circ. to polyg. meshes, 150–250 µm diam.; +Ch. +with loose multisp. tracts, forming circ. meshes, 100–150 µm diam. + +Holotype: +Panamá, Bocas del Toro, 14 m +
+ + +N. cylindrica +(Lamarck, 1815) + + +( +sensu +Topsent, 1933) + +H. +ramose; +S. +n.r.; +Cv. +ext. grayish with brown tinges, int. white; +Cs. +hard, fragile; +O. +n.o.; +E. +n.r.; +Ch. +retic., with large meshes of spongin-less multispic. tracts. + +Oxeas: +120–165/ 4–6 µm +Caribbean/ n.r.
+H. +thin to thick crusts, or 1–2 mm thick, coalescing branches, up to 10–15 cm high; +S. +dens. retic., or with scatt. grooves that converge and cut through the rim of the oscules, of lumpy or incomplete appear.; grooves may surround sooth, variably large knobs; +Cv. + +Oxeas. +86–198/2.8–10.5 µm + +Holotype. +Panamá, Bocas del Toro/2 m. +Paratypes. +Colombia/1.5–24 m. +Additional material. +Bocas del Toro, Panamá/5 m. +
+ + +N. dendrocrevacea +Vicente, Ríos, Zea & Toonen, 2019 + + +(orig. descr) + +ext. golden-yellow, reddish-brown, or dark purple with ochre-yel- low tinges; +Cs. +slightly soft to firm, crumbly; +O. +1–2 mm in crusts, to 5 mm in branching specs.; with transp. chimneys, occas. shut; +E. +paratang. retic., with confused, loose, uni- to paucispic. tracts, forming polyg. meshes, 100–200 µm diam, and spics. piercing surf.; +Ch. +confused, anisotrop. retic. with loose prim. tracts, interconn. by single spics. or loose paucispic. tracts, meshes 80–300 µm diam. +
+
+ +......continued on the next page ......continued on the next page ......continued on the next page + + +TABLE 2. (Continued) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Species +H. += habitus; +S. += surface; +Cv. += color +in vivo +; +Cs. += consistency; +O. += oscules; +E. += ectosome; +Ch. += choanosome; +n.o. += not ob- served; +n.r. += not reported + +Spicules + +Locality/ Depth +
+ + +N. dominicana + +(Pulitzer-Fi- nali, 1986) + +(orig. descr.) + +H. +sub-cylind.; +S. +n.r.; +Cv. +n.r.; +Cs. +cork-like when dry; +O. +scarce and aligned (2 mm diam.); +E. +retic. of spic. tracts forming loose meshes +( +350 µm diam.); +Ch. +irreg. retic. +( +meshes 500–700 µm wide), obscured by abund. scatt. single spics. + +Strongyles: +140–260/ 5–14 µm +Boca Chica (Dominican Republic), Caribbean/ 20 m
+Oxeas: +165–235–264/ 11–14–18 µm +Bonaire (The Netherlands), Caribbean/ 217 m
+ + +N. dutchi +van Soest, Meesters & Becking, 2014 + + +(orig. descr.) + +H. +bush-like with lobes; +S. +smooth with subdermal canals; +Cv. +pale beige; +Cs. +n.r.; +O +. apical (0.8–1.5 cm diam.); +E. +unspec.; +Ch. +dense, with squared anisotrop. meshes (200–259 µm wide). +
+Oxeas: +160–187–200/5–9–10 µm +Bonaire (The Netherlands), Carib- bean/108 m
+H. +vase shaped, larger specs. with wide, flaring walls; +S. +rough, with shallow depressions, red zoanthids often pres. on outer surf.; +Cv. +
+ + +N. eurystomata +van Soest, Meesters & Becking, 2014 + + +(orig. descr.) + +ext. pink and white, int. dark-red or brownish; +Cs. +firm and crum- bly, slightly compress.; +O. +n.r.; +E. +vague tang. retic. of 1–3 aligned spics, over regul. distrib. subderm. spaces (200–400 µm diam.); +Ch. +isotrop., with superimp. anisotrop. orient., with little or no visible spongin +
+
+ +TABLE 2. (Continued) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Species +H. += habitus; +S. += surface; +Cv. += color +in vivo +; +Cs. += consistency; +O. += oscules; +E. += ectosome; +Ch. += choanosome; +n.o. += not ob- served; +n.r. += not reported + +Spicules + +Locality/ Depth +
+Oxeas: +200–235–270/ 10.5– 14.5–15 µm +Klein Curaçao (Curaçao), Caribbean/ 149 m
+ + +N. ovata +van Soest, Meesters & Becking, 2014 + + +(orig. descr.) + +H. +ovate; +S. +smooth; +Cv. +pinkish-beige; +Cs. +firm; +O. +single, apical, with chimney (1.5 cm diam.); +E. +n.r.; +Ch. +dense, with rounded meshes +
+H. +cylind., flat branching, or thick. encrust. mounds; +S. +velvety, even, smooth, rugged, knobby (conic. or blunt elevs. around oscs., mass. specs. often w/ keyhole or irreg. grooves); +Cv. +ext. + +Oxeas: +92–205/1.7–12 µm +
+ + +N. proxima +( +Duchassaing & Michelotti, 1864 +) + + +( +sensu +Vicente, Ríos, Zea & Toonen, 2019 +) + +yellow(ish), (purplish) dark-brown, pink, light-purple, violet, int. light-yellow; +Cs. +tough., compress., hard to tear; +O. +2–7 mm diam., scatt. or aligned on ridges, w/wo chimney; +E. +fascicul. retic. of isotrop. multispic. tracts (20–200 µm), and circ. to irreg. elong. meshes (120–400 µm diam.), w/ radiat. spic. brushes at surf., w/wo subect. spaces (250–500 µm) +Ch. +w/ variably abund. circ. meshes (200–700 µm diam.) +Bocas del Toro, Panamá/8–14 m; Co- lombia, 25–36 m
+H. +thick crust, massive, ramose/cylind., or globular; +S. +irreg.; +Cv. +ext. red wine, beige, white, int. beige or red-wine; +Cs. +hard, friable; +
+( +sensu +present study) + +O. +scatt. (1–3 mm diam.), flat or apical on volcaniform projs.; +E. +isotrop. tang. retic. of pauci- to multisp. tracts (40–115 µm thick), rounded meshes (145–340 µm diam.); +Ch. +dense isotrop. retic., with loose multispic. tracts (100–270 µm thick), w/wo rounded, overlapp. meshes (195–435 µm diam.), with canals (390–580 µm diam.) + +Oxeas: +91–153 (15.2)–218/ 2–7 (1.7) 10 µm +Amapá, Bahia and Rio de Janeiro states (Brazil)/ 5.3–91 (250–500) m
+
+ +......continued on the next page + + +TABLE 2. (Continued) + + + + + + + + + + + + + + + + + + + + + + + + + + +
Species +H. += habitus; +S. += surface; +Cv. += color +in vivo +; +Cs. += consistency; +O. += oscules; +E. += ectosome; +Ch. += choanosome; +n.o. += not ob- served; +n.r. += not reported + +Spicules + +Locality/ Depth +
+Oxeas: +100–183.6–212/ 0.8–9.4– 15.6 µm +
+ + +N. rosariensis +Zea & Rützler, 1983 + + +(orig. descr.) + +H. +massive with cylind. tubes; +S. +smooth with rugose, protruding regions; +Cv. +ext. dark-brown, int. yellowish; +Cs. +hard, not elastic, friable; +O. +apical (0.7–2.4 cm diam.); +E. +isodyct. retic. of polyg. or triang. meshes (30–260 µm wide); +Ch. +isodyct., cavernous +Nossa Senhora do Rosário Archipelago (Colombian Caribbean) / 30 m
+H. +group of tubes, chimneys, ramified, erect, anastom. mounds, up to 10–30 cm width/height; +S. +smooth, w/wo horizont. crests, porous (0.5–1 mm diam.), occas. retic.; +Cv. +ext. brownish-amber, yellow with occas. brownish-green blotches, crimson with light and dark tones, base and int. light-yellow; +Cs. +firm, rigid, tough to cut, brittle; + +Oxeas: +130–260/5–18 µm +C-shaped sigmas: +8–21–33 µm +Caribbean: Panama, Colombia, Marti- nique/ 3–270 m
+ + +N. sigmafera +Vicente, Ríos, Zea & Toonen, 2019 + + +(orig. descr) + +O. +often apical (1–5 mm or 10–20 mm diam), w/wo translucent chimney; +E. +partially tang., isodict., with uni- or paucispic. tracts, with spongin at nodal points where ascend. choan. tracts connect with perpend. spic., cyanobacteria pigments penetrate about 1 mm.; +Ch +. anisotrop. retic. with ascend. multispic. tracts (thinner the closer to surf.), obscured by free spics., and occas. lacunae (130–250 µm diam.), interconn. by single or loosely bundled spics., with channels (0.3–2 mm diam.) +
+
+ +TABLE 2. (Continued) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Species +H. += habitus; +S. += surface; +Cv. += color +in vivo +; +Cs. += consistency; +O. += oscules; +E. += ectosome; +Ch. += choanosome; +n.o. += not ob- served; +n.r. += not reported + +Spicules + +Locality/ Depth +
+H. +sprawling w/ upright, tubif. projs., stiff bushes, or flabell./lamell. masses; +S. +smooth, but slight. rough to touch; +Cv. +red, brown-red, brown, or greenish; +Cs. +hard, incompress.; +O. +flush with surf. or + +Oxea ( +with rare strongylote or stylote modifications) 121– 159.5–186/3.5–5.9–8.5 µm. +Caribbean: Curaçao, Barbados, Puerto Rico, Florida/ 0–100 m
+ + +N. subtriangularis + +Duchassa- ing, 1850 + +( +sensu +Van Soest, 1980 +) + +apical at volcanif. elevs. (2–5 mm diam.); +E. +tangent. uni./plurispic. retic., in between protrud. choan. fibre-brushes; meshes 150–200 µm diam.; +Ch. +choan. skel. w/ prim. ascend. tracts and second. intercon- nect. tracts apparent in periph. regions, but increasingly obsc. to- wards the interior by superimp. isotrop. retic. wo/ definite orient., w/ rounded irreg. meshes, spic. tracts paucispic. w/ little or no spong. (many loose interst. spics., occasion. lead. to confused archit.). +
+H. +branch. fragms.; +S. +smooth, punctate, w/ faint subderm. grooves; + +Oxeas: +132–202–240/6–8.1–9.5 µm +Suriname/ 25–68 m
+( +sensu +Van Soest, 2017 +) + +Cv. +n.r.; +Cs. +firm; +O +. small, scatt. (2 mm diam.); +E. +reg. distrib. rounded / squar. meshes, tracts 1–3 spics. thick; +Ch. +denser, tracts 30–40 µm diam., squarish meshes up to 150–200 µm diam. +
+Oxeas: +119.0–157.5–193.0/ 2.8–4.9–9.6 µm +
+ + +N. sulcata +Santos, Sandes, Cabral & Pinheiro, 2016 + + +(orig. descr.) + +H. +irreg. cylind.; +S. +rugose, sulcate, punctif.; +Cv. +n.r.; +Cs. +hard, very fragile; +O. +flush w/ surf. (1.5–4.0 mm diam.); +E. +retic. w/ rounded meshes +( +150–300 µm diam.), w/ multispic. tracts (50–250 µm diam.); +Ch. +anisotrop. over isotropic retic. +Maranhão and Rio Grande do Norte States (Brazil)/ 70–101 m (Brazil)/ 70–101 m
+
+ + +FIGURE 2 + +Neopetrosia proxima +( +Duchassaing & Michelotti, 1864 +) + +. (A) thick anatomical sections and dissociated spicules slides, (B) +in situ +image, (C–D) ectosome, (E–F) choanosome, (G, I) oxeas, (H, J) details of oxea extremities. A, C, E, G–H, Schizolectotype BMNH 1928.XI.12.45a; B, D, F, I–J, MNRJ 10526. Scale bars, (B) 1 cm, (C–D) 100 µm, (E–F) 150 µm, (G–H, J) 10 µm, (I) 50 µm. + + + +External morphology. +Thickly encrusting to massive, ramose/cylindrical, and globular ( +Fig.2B +), reaching over +20 cm +diam. in the field. Largest preserved specimen 7.4 x 3.3 x +2.7 cm +( +MNRJ +8427). Irregular surface with scattered oscules ( +1–3 mm +diam.) on it or apical on volcano-like projections. Two specimens ( +MNRJ +2606 and 8419) showed two terminal oscules each (0.6–1.0 mm diam.). Hard and friable consistency; microhispid texture to the touch. Color +in vivo +red wine (whole or with beige interior), beige, white (whole or with red-wine interior); becoming beige-orange or light brown in ethanol. + +
+ + +Skeleton. +Ectosome arranged in an isotropic tangential reticulation forming rounded meshes ( +145–340 µm +diam.) of pauci- to multispicular tracts ( +40–115 µm +thick) ( +Fig. 2C, D +). Choanosome densely reticulated, isotropic, with loose multispicular tracts ( +100–270 µm +thick) forming rounded overlapping meshes ( +195–435 µm +diam.), which are poorly defined in some regions. Canals present ( +390–580 µm +diam.) ( +Fig. 2E, F +). + + +Spicules. +Oxeas in one size class (91–155 (15)–216/ 2–7 (1.9)– +15 µm +), smooth, slightly curved to straight, usually with acerate edges that vary to hastate and rounded ( +Fig. 2G–J +) ( +Table 1 +). + + + + +Ecology. +The species was previously known from +0.5–153 m +depth ( +Zea 1987 +; +Van Soest & Stentoft 1988 +); which is here expanded down to +250–500 m +depth, based on a deep record for the Almirante Saldanha Seamount, growing over rhodolith beds. MNRJ 5998 and UFRJPOR 933 were associated to + +Parazoanthus +(Zoantharia) + +. Specimen MNRJ 10526 faced considerable silting. + + + + +Distribution. +Tropical Atlantic. +Brazil +: +Amapá State +(off the Amazon River mouth, + +Mothes +et al. +2006 + +; +Fig. 1 +); +Maranhão State +( + +Campos +et al. +2005 + +); +Rio Grande do Norte State +( + +Muricy +et al. +2008 + +); +Sergipe State +( + +Santos +et al +. 2016 + +); +Bahia +and +Rio de Janeiro +States (Almirante Saldanha Seamount) (present study, +Fig. 1 +). Caribbean ( +Duchassaing & Michelotti 1864 +; + +Van Soest +et al +. 1983 + +; +Zea 1987 +; +Van Soest & Stentoft 1988 +; +Lehnert & Van Soest 1996 +; + +Rützler +et al +. 2000 + +; +Díaz 2005 +; + +Pérez +et al +. 2017 + +; + +Vicente +et al. +2019 + +). +Suriname +( +Van Soest 2017 +). + + + + +Remarks. +The species’ habit observed on Brazilian specimens repeats what has been reported from Caribbean materials described by +Zea (1987) +and + +Vicente +et al +. (2019) + +, and is summarized in +Table 2 +. Specimens can be thickly encrusting, cushion-shaped, to erect, irregularly ramified with short cylindrical branches. The species has been reported with several distinct colors (e.g. +Zea 1987 +; +Van Soest & Stentoft 1988 +; +Lehnert & Van Soest 1996 +; + +Vicente +et al. +2019 + +), which is partially matched by specimens herein described. In general lines, Brazilian specimens appear to be more on the red-wine (maroon, burgundy) spectrum of color, rather than on the brownish side. But brownish tinges appear here and there. +Lehnert & Van Soest (1996) +suggested this color variation might be a response to light availability in different depths, which is supported by +Zea’s (1987) +observation that specimen INV-POR 0210, which was living in a small cave, was lilac, nearly white. Additional shared features between the schizolectotype and Brazilian specimens were the reticulated skeleton formed by rounded meshes, and the slightly curved oxeas with hastate edges and similar dimensions (91–161 vs +97–194 µm +, respectively; +Fig. 2C–F +). The comparison between + +N. proxima + +and the recently described + +N. sulcata + +Santos +et al +., 2016 + + +was detailed in the original description of the latter species, and we favor any further comparison between both to take molecular data into account. + + +
+
\ No newline at end of file diff --git a/data/38/5D/87/385D87B7FFB2F8742D94F94FFC58FE70.xml b/data/38/5D/87/385D87B7FFB2F8742D94F94FFC58FE70.xml new file mode 100644 index 00000000000..080606e7b00 --- /dev/null +++ b/data/38/5D/87/385D87B7FFB2F8742D94F94FFC58FE70.xml @@ -0,0 +1,510 @@ + + + +Taxonomy of Petrosiidae Van Soest, 1980 (Haplosclerida, Porifera) from Brazil + + + +Author + +Rocha, Lívia +0000-0002-5284-1309 +liviahrocha @ yahoo. com. br; https: // orcid. org / 0000 - 0002 - 5284 - 1309 +liviahrocha@yahoo.com.br + + + +Author + +Moraes, Fernando +0000-0001-8251-6868 +fmoraes @ mn. ufrj. br; https: // orcid. org / 0000 - 0001 - 8251 - 6868 +fmoraes@mn.ufrj.br + + + +Author + +Salani, Sula +0000-0003-3850-1030 +Laboratório de Bentos, Instituto de Ciências Biológicas, Universidade de Brasília. Campus Universitário Darcy Ribeiro, Bloco E, s / n, Asa Norte, CEP 70910 - 900, Brasília / DF, Brazil. & sulasm @ gmail. com; https: // orcid. org / 0000 - 0003 - 3850 - 1030 +sulasm@gmail.com + + + +Author + +Hajdu, Eduardo +0000-0002-8760-9403 +eduardo. hajdu @ gmail. com; https: // orcid. org / 0000 - 0002 - 8760 - 9403 +eduardo.hajdu@gmail.com + +text + + +Zootaxa + + +2021 + +2021-07-20 + + +5004 + + +2 + + +251 +287 + + + +journal article +10.11646/zootaxa.5004.2.2 +1175-5326 +5677189 +B1B2F144-2B51-4079-ACB5-6D78B38B32E7 + + + + + + + +Xestospongia dorigo + +sp. nov. + + + + + + +( +Fig. 1 +, +7 +; +Tab. 7 +) + + + + + + +Holotype +. + +Brazil +, +Alagoas State +, +MNRJ 15405 +, +Francês Beach +( +9.76725º S +, +35.83610º W +, Marechal Deodoro), + +2.9 m +depth + +, +Col. E. Hajdu +, + +2011.9.15 + + +. + + +Paratypes +( +two specimens +). + +Ceará State + +, + +MNRJ 20131 +, +Boi Choco Beach +( +03.68753º S +, +38.61034º W +, Dois Coqueiros, Caucaia), + +1 m +depth + +, +Col. A. Bispo +& +S. Salani +, + +2016.4.11 + + +. + +Alagoas State +(type locality), +MNRJ 21029 +, 2– + +4 m +depth + +, +Col. A. Bispo +, + +2016.12.19 + + +. + + + + +Diagnosis. +This is the only Tropical Western Atlantic + +Xestospongia + +with a cushion-shape, no projections, with relatively small oscula ( +2–3 mm +diam.), and white to beige colour +in vivo +. Megascleres are oxeas with acerate, hastate and mucronate ends, 300–450/ +5–15 µm +. + + +External morphology. +Cushion-shaped, up to +12 cm +in diameter ( +Fig. 7A–B +). Surface smooth to the naked eye, irregular, without any marked projections, but rough to the touch. Rare, circular oscules ( +2–3 mm +diam.). Consistency firm, slightly compressible, and fragile. Colour +in vivo +light yellowish-white ( +holotype +), light grayish-brown (MNRJ 20131), or light yellowish-beige (MNRJ 21029), becoming a light shade of gray or beige after fixation. + + +Skeleton. +Ectosomal, an isodyctial, isotropic reticulation ( +Fig. 7C +) with uni- to paucispicular tracts (up to +63 µm +thick), forming (sub)triangular meshes ( +65–195 µm +wide). Choanosomal, similar, but denser than the ectosomal, tracts +30–90 µm +thick, meshes +110–230 µm +wide ( +Fig. 7D +); aquiferous canals seen here and there ( +520–1,775 µm +wide). + + +Spicules. +Oxeas in a single size class, smooth, slightly curved, with hastate, acerate and mucronate edges: 294–369 (22)–445/ 5–10 (2)– +15 µm +( +Fig.7E–F +; +Tab.7 +). + + + + +TABLE 7. +Spicule measurements of + +Xestospongia dorigo + + +sp. nov. + +Values given in min.–med. (SD)–max. + + + + + + + + + + + + + + + + + + + + +
+Specimens + +Oxeas (length/ width) +
Holotype MNRJ 15405 Alagoas363–398 (21.8)–445/ 10–13 (2.2)–15 µm
Paratype MNRJ 20131 Ceará294–339 (22)–388/ 5–7 (1.7)–9 µm
Paratype MNRJ 21029 Alagoas305–369 (26.6)–431/ 10–11 (2)–15 µm
+
+ + +Ecology. +The species occurs in association with other sponge species, tunicates, ophiuroids and mollusks, between 1 and +4 m +depth. + + + + +Etymology. +The specific epithet is used as a noun in apposition, and honors Prof. Dr. Monica Dorigo Correia, prematurely deceased, a long-time collaborator and friend of the authors. + + + + +Type locality. +Marechal Deodoro (Francês Beach), +Alagoas State +, +Brazil +. +Additional distribution. +Provisional Brazilian endemic, also known from +Ceará State +(Caucaia). + + +Taxonomic remarks. +There are only 11 shallow and relatively shallow-water species of + +Xestospongia + +in the Tropical Western Atlantic (see + +Carvalho +et al. +2016 + +). These include + +X. deweerdtae +, + + +X. portoricensis +Van Soest, 1980 + +and + +X. rampa +de Laubenfels, 1934 + +(the latter deemed to be a junior synonym of + +X. muta + +by +Zea 1987 +), which possess strongyles instead of oxeas as their megascleres; as well as + +X. bocatorensis + +Diaz +et al. +, 2007 + + +, which possesses sigma microscleres. All four species are regarded quite distinct from + +X. dorigo + + +sp. nov. + +Considerably smaller spicules than seen in + +X. dorigo + + +sp. nov. + +differentiate + +X. menzeli +Little, 1963 + +from our new species as well. + + +The remaining five species are + +X. arenosa +van Soest & de Weerdt, 2001 + +, + +X caminata +Pulitzer-Finali, 1986 + +, + +X. muta +( +Schmidt, 1870 +) + +, + +X. purpurea +Rützler, Piantoni, Van Soest & Diaz, 2014 + +and + +X. wiedenmayeri +van Soest, 1980 + +. + +Xestospongia arenosa + +was originally reported as comprising “clusters of short irregular tubes and closed digitations, and smaller fistules rising from a massive base, which is usually entirely covered by sediment, rubble and shells” (cf. +Van Soest & de Weerdt 2001 +). Overall, this habit is notoriously distinct from the nearly flat, only thickly encrusting habit observed in + +X. dorigo + + +sp. nov +. + +, which, furthermore possesses only rare, rather small ( +2–3 mm +diam.) oscula, contrasting to the large oscula (up to +15 mm +diam.) reported for + +X. arenosa + +( +van Soest & de Weerdt 2001 +, + +Rützler +et al. +2014 + +, +Silva & Zea 2017 +). + +Xestospongia caminata + +usually has a smooth surface and large ( +5–9 mm +diam.) oscula, bearing megascleres of varied form, mostly oxeas, but ranging to styles and strongyles. Its megascleres were reported to be considerably smaller ( +200–280 µm +, +Pulitzer-Finali 1986 +) than those in + +X. dorigo + + +sp. nov. + +, but a subsequent record of the species by +van Soest & de Weerdt (2001) +found megascleres as large as +370 µm +, thus approaching the size of spicules seen in the new species. However, we consider the sponge habit sufficiently characteristic to preclude their possile cospecificity, strenghtened by the fact that + +X. caminata + +is reported to be dark coloured +in vivo +, while + +X. dorigo + + +sp. nov +. + +is light-coloured. + +Xestospongia muta + +, known as the great-barrel sponge, is markedly distinct from the new species, even when quite young, for its purplish-rose colour +in vivo +. Besides, the strongyles present in the majority of Brazilian specimens studied, which on one side are only occasionally modified into strongyloxeas, and on the other are much stouter (with the means of spicule widths being around +18 µm +), support differentiating the two species. + +Xestospongia purpurea + +, in addition to its distinctive spotted purple colour +in vivo +, has much stouter megascleres, thus appearing quite distinct from the new species too. Megasclere thickness is well known to be directly dependent on proximity from continental sources of silica in the wider Caribbean region (e.g. +Zea 1987 +), and accordingly, this is a character to be looked at cautiously. In the case of + +X. purpurea + +, both records are from continental sites ( +Belize +and Cartagena; respectively + +Rützler +et al. +2014 + +; +Silva & Zea 2017 +), optimal surrogates for the confirmation of the species’ ability to produce thicker spicules. As + +X. dorigo + + +sp. nov. + +also occurs in coastal and supposedly silica rich waters (Ceará and Alagoas States), we consider the distinctness of both species ability to build thick spicules to be of diagnostic importance. Lastly, + +X. wiedenmayeri + +approaches the new species considerably. Points of distinction are the presence of cylindrical projections and hollow fistules, the dark brownish-red colour in the fixative, and somewhat thicker oxeas of the latter species from +Curaçao +. Given the above comparisons, we are confident that + +X. dorigo + + +sp. nov. + +is a new species. + + +
+
\ No newline at end of file diff --git a/data/38/5D/87/385D87B7FFB9F8722D94F959FBBAFA86.xml b/data/38/5D/87/385D87B7FFB9F8722D94F959FBBAFA86.xml new file mode 100644 index 00000000000..0bf82af8b80 --- /dev/null +++ b/data/38/5D/87/385D87B7FFB9F8722D94F959FBBAFA86.xml @@ -0,0 +1,715 @@ + + + +Taxonomy of Petrosiidae Van Soest, 1980 (Haplosclerida, Porifera) from Brazil + + + +Author + +Rocha, Lívia +0000-0002-5284-1309 +liviahrocha @ yahoo. com. br; https: // orcid. org / 0000 - 0002 - 5284 - 1309 +liviahrocha@yahoo.com.br + + + +Author + +Moraes, Fernando +0000-0001-8251-6868 +fmoraes @ mn. ufrj. br; https: // orcid. org / 0000 - 0001 - 8251 - 6868 +fmoraes@mn.ufrj.br + + + +Author + +Salani, Sula +0000-0003-3850-1030 +Laboratório de Bentos, Instituto de Ciências Biológicas, Universidade de Brasília. Campus Universitário Darcy Ribeiro, Bloco E, s / n, Asa Norte, CEP 70910 - 900, Brasília / DF, Brazil. & sulasm @ gmail. com; https: // orcid. org / 0000 - 0003 - 3850 - 1030 +sulasm@gmail.com + + + +Author + +Hajdu, Eduardo +0000-0002-8760-9403 +eduardo. hajdu @ gmail. com; https: // orcid. org / 0000 - 0002 - 8760 - 9403 +eduardo.hajdu@gmail.com + +text + + +Zootaxa + + +2021 + +2021-07-20 + + +5004 + + +2 + + +251 +287 + + + +journal article +10.11646/zootaxa.5004.2.2 +1175-5326 +5677189 +B1B2F144-2B51-4079-ACB5-6D78B38B32E7 + + + + + + + +Xestospongia muta +( +Schmidt, 1870 +) + + + + + + + +( +Fig. 1 +, +5–6 +; +Tab. 6 +) + + + + + + +Xestospongia muta +, De Laubenfels 1936: 70 + +; + +Van Soest 1981: 21 + +; + +Vacelet 1990: 29 + +; + + +Rützler +et al +., 2009: 289 + + +; + + +Hajdu +et al +. 2011: 198 + + +; + +Moraes 2011: 187 + +; + +Alcolado & Busutil 2012: 71 + +; + +Moura +et al +. 2016 + +: Supplementary Table; + + +Pérez +et al +. 2017: 10 + + +; + +Van Soest 2017: 40 + +. + + + +Prianus +sp., +Hechtel 1976: 252 +. + + + + +Prianus grayi +Hechtel, 1983 + +— + +Hechtel 1983: 64 + +, fig. 4. + + + + + + +Xestospongia grayi +, +Mothes & Bastian 1993: 23 + + +; Santos +et al. +2002b: 396; + + +Moraes +et al. +2006: 169 + + +. + + + +Additional synonymy in + +Muricy +et al +. 2011: 106 + +. + + + + + +Studied material ( +24 specimens +). + + +Brazil +, off +Pará State +, +MNRJ 16585 +, +Station +AMZ-4 ( +1.31683º N +, +46.83370º W +, + + +Amazon +River + +Mouth + +), + +55.9 m +depth + +, Coll. +R +. +Moura +& +N. Oliveira +/ +R +/ +V +‘ +Atlantis’ +, + +2012.7.25 + +. +Maranhão State +: +MNRJ 8722 +, +Mar XV Stn +47 ( +1.33333º S +, +43.56667º W +), + +62 m +depth + +, +Coll. N +/Rb. ‘Victor Hensen’, + +1990.11.10 + +. +Pernambuco State +, +Fernando de Noronha Archipelago +: +MNRJ 7924 +, Cagarras Fundas ( +3.80790º S +, +32.39009º W +, +Rata Island +), + +20 m +depth + +, +Coll. G. Muricy +, + +2003.11.9 + +; +MNRJ 7770 +, Cagarras Fundas ( +3.80790º S +, +32.39009º W +, +Rata Island +), + +18 m +depth + +, +Col. F. Moraes +, + +2003.11.13 + +; +MNRJ 7771 +, Cagarras Funda ( +3.80790º S +, +32.39009º W +, +Rata Island +), + +22 m +depth + +, +Coll. E. Hajdu +, + +2003.11.13 + +; +MNRJ 7894 +, Cagarras Fundas ( +3.80790º S +, +32.39009º W +, +Rata Island +), + +15 m +depth + +, +Col. G. Muricy +, + +2003.11.8 + +; +MNRJ 7897 +, +Ponta das Caracas +( +3.87828º S +, +32.42498º W +, +Fernando de Noronha Island +), depth not recorded, +Coll. F. Moraes +, + +2003.11.21 + +; +MNRJ 7950 +, Cagarras Rasa ( +3.80790º S +, +32.39009º W +, +Rata Island +), + +20 m +depth + +, +Coll. G. Muricy +, + +2003.11.13 + +; UFRJPOR 3920, precise locality not recorded, + +40 m +depth + +, +Coll. G. Muricy +, + +1996.3.1 + +; UFRJPOR 4779, Lage Dois Irmãos ( +3.84710º S +, +32.45014º W +, +Fernando de Noronha Island +), + +15 m +depth + +, +Coll. G. Muricy +, + +1998.2.15 + +. +Bahia State +(all from REVIZEE/ Central-SCORE, +Coll. N +/Rb. ‘Astro Garoupa’): +MNRJ 3109 +, Station 15 +R +, Campaign 2 ( +18.02306º S +, +35.89111º W +, Hotspur Bank), + +60 m +depth + +, + +1997.11.13 + +; +MNRJ 3392 +, D0404, Campaign BA-1, Sample 1C ( +17.13438º S +, +36.80553º W +, Rodger Bank), + +39.2–65.2 m +depth + +, + +1999.6.6 + +; +MNRJ 3697 +A, Station 10 +R +, Campaign 2 ( +17.08889º S +, +36.75194º W +, Rodger Bank), + +50 m +depth + +, + +1997.11.14 + +; +MNRJ 4580 +, Station 14 +R +, Campaign 5 ( +17.80000º S +, +35.87500º W +, Hotspur Bank), + +60 m +depth + +, + +2001.7.7 + +; +MNRJ 4783 +, Station 10 +R +, Campaign 5 ( +17.10306º S +, +36.74111º W +, Rodger Bank), + +50 m +depth + +, + +2001.7.7 + +. +Bahia State +: +MNRJ 8319 +, Todos os +Santos Bay +, ‘Germânia’ Shipwreck ( +13.00861º S +, +38.54389º W +, Salvador), + +5 m +depth + +, +Coll. E. Hajdu +, + +2004.6.3 + +; +MNRJ 13104 +, Boião (beacon signalling buoy) off + +Farol +da Barra + +( +13.00866º S +, +38.54388º W +, +Salvador +), + +15.8 m +depth + +, +Coll. E. Hajdu +& +C. Castello-Branco +, + +2009.6.3 + +. Off Espírito Santo State (all from REVIZEE/ Central-SCORE, Vitória-Trindade Seamounts chain, +Coll. N +/Rb. ‘Astro Garoupa’): +MNRJ 4396 +, Station 23 +R +, Campaign 5 ( +20.48694º S +, +36.10306º W +, Jaseur Bank), + +55 m +depth + +, + +2001.7.12 + +; +MNRJ 4407 +, Station 28 +R +, Campaign 5 ( +19.80806º S +, +37.93889º W +, Besnard Bank), + +60 m +depth + +, + +2001.7.18 + +; +MNRJ 4900 +, Station 45 +R +, Campaign 5 ( +20.40119º S +, +39.91655º W +, off Vila Velha), + +108 m +depth + +, + +2001.7.12 + +; UFRJPOR 4394, +Station C +61, Campaign 1 ( +20.50611º S +, +37.31806º W +, Congress Bank), + +88 m +depth + +, + +1996.4.24 + +; +MNRJ 5891 +, Station 34 +R +, +Campaign +5 ( +20.40194º S +, +39.92306º W +, off +Vila Velha +), + +50 m +depth + +, + +2001.7.15 + +. +Off Rio de Janeiro State +(all from +Almirante Saldanha Seamount +, +Station Y +2, +Campaign +6, REVIZEE/ Central-SCORE, +22.38194º S +, +37.58806º W +, + +270 m +depth + +, +Coll. N +/ +Rb. +‘ +Astro Garoupa’ +, + +2002.6.12 + +): +MNRJ 6011 +, +6090 +, +7223 + +. + + +Comparative Material. + +Prianos grayi +Hechtel, 1983 + +, +Holotype +YPM +9008 ( +Brazil +, +Pernambuco State +, Fernando de Noronha Archipelago, +3.85000º S +, +32.43333º W +), Coll. J. Laborel, Schizolectotype +MNRJ +14959. + +Xestospongia grayi + +— +Mothes & Bastian (1993: 23) +, MCN 1327, +Brazil +, +Pernambuco State +, Fernando de Noronha Archipelago, Ponta da Sapata, +25 m +depth, Coll. C. Castro & D.O. Pires, +1986.06.11 +. + + + + \ No newline at end of file diff --git a/data/38/5D/87/385D87B7FFB9F87D2D94FB19FF02F947.xml b/data/38/5D/87/385D87B7FFB9F87D2D94FB19FF02F947.xml new file mode 100644 index 00000000000..83888dafd52 --- /dev/null +++ b/data/38/5D/87/385D87B7FFB9F87D2D94FB19FF02F947.xml @@ -0,0 +1,156 @@ + + + +Taxonomy of Petrosiidae Van Soest, 1980 (Haplosclerida, Porifera) from Brazil + + + +Author + +Rocha, Lívia +0000-0002-5284-1309 +liviahrocha @ yahoo. com. br; https: // orcid. org / 0000 - 0002 - 5284 - 1309 +liviahrocha@yahoo.com.br + + + +Author + +Moraes, Fernando +0000-0001-8251-6868 +fmoraes @ mn. ufrj. br; https: // orcid. org / 0000 - 0001 - 8251 - 6868 +fmoraes@mn.ufrj.br + + + +Author + +Salani, Sula +0000-0003-3850-1030 +Laboratório de Bentos, Instituto de Ciências Biológicas, Universidade de Brasília. Campus Universitário Darcy Ribeiro, Bloco E, s / n, Asa Norte, CEP 70910 - 900, Brasília / DF, Brazil. & sulasm @ gmail. com; https: // orcid. org / 0000 - 0003 - 3850 - 1030 +sulasm@gmail.com + + + +Author + +Hajdu, Eduardo +0000-0002-8760-9403 +eduardo. hajdu @ gmail. com; https: // orcid. org / 0000 - 0002 - 8760 - 9403 +eduardo.hajdu@gmail.com + +text + + +Zootaxa + + +2021 + +2021-07-20 + + +5004 + + +2 + + +251 +287 + + + +journal article +10.11646/zootaxa.5004.2.2 +1175-5326 +5677189 +B1B2F144-2B51-4079-ACB5-6D78B38B32E7 + + + + + + + +Xestospongia kapne +Carvalho, Lopes, Cosme & Hajdu, 2016 + + + + + + + +Studied material: + + +Holotype +, + +Brazil +, off +Rio de Janeiro State +: +MNRJ 13541 +, +Caratinga Oil Field +( +22.623° S +, +40.264° W +, +Campos Basin +), + +923 m +depth + +, Col. ROV from the +R +/ +V +‘Toisa Conqueror’, + +2006.3.12 + +. + + + + + +Diagnosis. +Massive, robust, barrel- or chimney-shaped (clusters of up to three chimneys), with an irregular contour, up to +50 cm +tall, and a large apical pseudo-oscule. Surface with lobular projections and shallow depressions or gaps, and rough texture. Ectosome with a loose reticulation made by the tangentially disposed spicules of the terminal tufts of ascending choanosomal spiculo-fibers, with meshes seen here and there (140–250 μm diam). Cho- anosome a reticulation, clearly visible only in some areas, overlaid by abundant oxeas in confusion. Meshes only seldom observed (200–400 μm diam). Unclear distinction between primary and secondary fibres. Oxeas, relatively robust, usually slightly curved, tapering gradually, 204–301 x 11–14 μm [adapted from + +Carvalho +et al +. 2016 + +]. + + + + +Description. +Refer to + +Carvalho +et al +. (2016) + +. + + + + +Distribution. +Provisional Brazilian endemic, so far known only from off the State of +Rio de Janeiro +(Campos Basin). + + + + \ No newline at end of file diff --git a/data/38/5D/87/385D87B7FFBEF87D2D94FC45FC75FDE0.xml b/data/38/5D/87/385D87B7FFBEF87D2D94FC45FC75FDE0.xml new file mode 100644 index 00000000000..637698924c1 --- /dev/null +++ b/data/38/5D/87/385D87B7FFBEF87D2D94FC45FC75FDE0.xml @@ -0,0 +1,1167 @@ + + + +Taxonomy of Petrosiidae Van Soest, 1980 (Haplosclerida, Porifera) from Brazil + + + +Author + +Rocha, Lívia +0000-0002-5284-1309 +liviahrocha @ yahoo. com. br; https: // orcid. org / 0000 - 0002 - 5284 - 1309 +liviahrocha@yahoo.com.br + + + +Author + +Moraes, Fernando +0000-0001-8251-6868 +fmoraes @ mn. ufrj. br; https: // orcid. org / 0000 - 0001 - 8251 - 6868 +fmoraes@mn.ufrj.br + + + +Author + +Salani, Sula +0000-0003-3850-1030 +Laboratório de Bentos, Instituto de Ciências Biológicas, Universidade de Brasília. Campus Universitário Darcy Ribeiro, Bloco E, s / n, Asa Norte, CEP 70910 - 900, Brasília / DF, Brazil. & sulasm @ gmail. com; https: // orcid. org / 0000 - 0003 - 3850 - 1030 +sulasm@gmail.com + + + +Author + +Hajdu, Eduardo +0000-0002-8760-9403 +eduardo. hajdu @ gmail. com; https: // orcid. org / 0000 - 0002 - 8760 - 9403 +eduardo.hajdu@gmail.com + +text + + +Zootaxa + + +2021 + +2021-07-20 + + +5004 + + +2 + + +251 +287 + + + +journal article +10.11646/zootaxa.5004.2.2 +1175-5326 +5677189 +B1B2F144-2B51-4079-ACB5-6D78B38B32E7 + + + + + + + +Petrosia +( +Petrosia +) +revizee + +sp. nov. + + + + + + +( +Fig. 1 +, +4 +; +Tab. 4–5 +) + + + + + + +Holotype +. + +Brazil +, +Bahia State +, +MNRJ 22190 +, +Station +14 +R +(Hotspur Seamount, REVIZEE/ Central +SCORE +, Campaign 5, +17.80000º S +– +35.87500º W +), + +60 m +depth + +, +Col. N +/ +Rb. Astro Garoupa +, + +2001.8.7 + + +. + +Paratypes +( +8 specimens +). + + +Brazil +, +Bahia State +: +MNRJ 2652 +, +Boião +(beacon signalling) off + +Farol +da Barra + +( +13.00000º S +, +38.51667º W +, Salvador), + +16 m +depth + +, +Col. E. Hajdu +et al +., + +1999.8.8 + +; +MNRJ 10575 +, +Boião +(beacon signalling) off + +Farol +da Barra + +( +13.00000º S +, +38.51667º W +, +Salvador +), depth not recorded, +Col. E. Hajdu +, + +2007.12.12 + +; +MNRJ 13119 +, +Boião +(beacon signaling) off + +Farol +da Barra + +( +13.00000º S +, +38.51667º W +, Salvador), + +15.8 m +depth + +, +Col. E. Hajdu +& +C. Castello-Branco +, + +2009.6.3 + +. REVIZEE/ Central-SCORE, +Col. N +/ +Rb. Astro Garoupa +: +MNRJ 3274 +A, +Station +15 +R +(Hotspur Seamount, Campaign 2, +18.02306º S +, +35.89111º W +), + +60 m +depth + +, + +1997.11.13 + +; +MNRJ 4461 +, Station 14 +R +(Hotspur Seamount, Campaign 5, +17.80000º S +, +35.87500º W +), + +60 m +depth + +, +Col. N +/ +Rb. Astro Garoupa +, + +2001.8.7 + +; +MNRJ 4675 +, Station 2 +R +(off +Ponta de Castelhanos +, Campaign 5, +13.64611º S +, +38.74194º W +, +Morro de São Paulo +, Cairu), + +55 m +depth + +, + +2001.7.2 + +; +MNRJ 4793 +, +4851 +, Station 7 +R +(Royal Charlotte Bank, Campaign 5, +16.11694º S +, +38.17000º W +), + +40 m +depth + +, + +2001.6.30 + +; Espírito Santo State, +MNRJ 4897 +, Station 20 +R +(off Barra Seca, Campaign 5, +19.27194º S +, +38.01889º W +, Abrolhos Bank), + +67 m +depth + +, + +2001.6.28 + + +. + +Additional Material ( +14 specimens +). + + +Pernambuco State +: UFRJPOR 4043, +Tamandaré +, +Biquara Reef +( +8.75000º S +, +35.08333º W +), depth not recorded, +Col. G. Muricy +, + +1996.3.9 + + +. + +Alagoas State +: +MNRJ 17022 +(= +UFAL +POR 0832 +), +Marechal Deodoro +, +Cabeço da Pequena +( +9.76667º S +, +35.83333º W +), + +18 m +depth + +, +Col. M.D. Correia +, + +2012.2.19 + + +. + +All +of the following—REVIZEE/ Central-SCORE, +Col. N +/ +Rb. Astro Garoupa + +: + +Bahia State +(REVIZEE): +MNRJ 3117 +B, 3225A, +Station +11 +R +( +Rodger Bank +, +Campaign +2, +17.06011º S +, +36.80806º W +), + +50 m +depth + +, + +1997.11.14 + + +. + +Off Espírito Santo State +(REVIZEE): +MNRJ 4672 +, +Station +42 +R +( +Columbia Seamount +, +Campaign +5, +20.73806º S +, +31.82806º W +), + +85 m +depth + +, + +2001.7.11 + + +; + +MNRJ 4882 +, +Station +17 +R +(off +Itaúnas +, +Campaign +5, +18.66306º S +, +37.87000º W +), + +65 m +depth + +, + +2001.6.29 + + +; + +MNRJ 4928 +, +Station +25 +R +(off +Linhares +, +Campaign +5, +19.52694º S +, +38.76806º W +), + +65 m +depth + +, + +2001.6.28 + + +; + +MNRJ 4948 +, +5020 +, +Station +17 +R +(off +Itaúnas +, +Campaign +5, +18.66306º S +, +37.87000º W +), + +65 m +depth + +, + +2001.6.29 + + +; + +MNRJ 6572 +, +6574 +, +Station +C44 (off +Guarapari +, +Campaign +6, +20.63306º S +, +40.02500º W +), + +54 m +depth + +, + +2002.6.14 + + +. + +Off Rio +de + + +Janeiro State +, +Almirante Saldanha Seamount +(REVIZEE): +MNRJ 5981 +, +5973 +C, +Station +Y2 ( +Campaign +6, +22.38222º S +, +37.58750º W +), + +270 m +depth + +, + +2002.7.12 + + +; + +MNRJ 6595 +, +Station +Y2 ( +Campaign +6, +22.38194º S +, +37.58806º W +), + +270 m +depth + +, + +2002.6.12 + + +. + + + + +FIGURE 4. + +Petrosia +( +Petrosia +) +revizee + + +sp. nov +. + +(A) preserved holotype, (B) +in situ +image of specimen, (C) tangential section and morphological variation of the ectosome, (D) perpendicular section of choanosome, (E) oxeas II echinating the multispicular tracts of oxeas I, (F) oxeas I, (G) oxeas II, (H) details of the extremities of oxeas I, (I) details of the extremities of oxeas II. A, Holotype MNRJ 22190; B, Paratype MNRJ 13119; C–I, Paratype MNRJ 4461. Scale bars, (A–B) 1 cm, (C) 100 µm, (D) 150 µm, (E–I) 10 µm. + + + + +Diagnosis. +This is the only Western Tropical Atlantic + +Petrosia + +( +P. +) with two, and only two well-differentiated categories of oxeas, being also devoid of any microsclere categories. + + +External Morphology. +Massive to ramose, with thick lobes. +Holotype +with 16.5 x 9.8 x +3.4 cm +( +Fig. 4A–B +). Smooth and irregular surface. Oscules rounded ( +1–4 mm +diam.), dispersed over the entire surface, slightly raised or leveled with it. Some specimens presented a single terminal oscule at each lobe ( +4–8 mm +diam.). Texture rough to the touch. Consistency firm, slightly compressible, elastic or hard and incompressible. Color +in vivo +and after collection, pink, red-wine, light-brown or white; sometimes showing red-wine or purple tinges near the oscules. In alcohol the color varies among orange-beige, brown (both with cream interior) and red-wine. + + +Skeleton. +Ectosomal, a reticulated architecture of dense multispicular tracts in tangential section ( +25–165 µm +thick), specially of oxeas I, forming rounded/polygonal meshes ( +130–255 µm +wide), with oxeas II less abundant, and usually occurring among tracts ( +Fig. 4C +). In transverse section, perpendicular choanosomal spicule tracts pierce the ectosome, translating in a hispid texture of the sponge ( +Fig. 4D +). The subectosomal region carries abundant justaposed lacunae ( +290–390 µm +wide). Choanosomal, an anastomosing isotropic reticulation of dense multispicular tracts ( +50–390 µm +thick), composed mainly by oxeas I, forming oval to rectangular meshes ( +575–620 µm +wide), with oxeas II usually echinating the tracts ( +Fig. 4D; E +). Some specimens show meshes parallel to the surface (e.g. MNRJ 4851, 4897, 17022). Loose oxeas, of both size classes, are found among spicule tracts, as is abundant spongin and foreign material (e.g. sand grains). + + +Spicules. +Oxeas in two size classes. Oxeas I ( +Fig. 4F, H +), smooth, slender, slightly curved with usually rounded ends, but sometimes telescopic or mucronate, 102–206 (25)–305/ 5–7 (1.4)– +19.4 µm +. Oxeas II ( +Fig. 4G, I +; +Table 4 +), resembling the former, but smaller and less abundant, 39–68 (10)–97/ 5–5 (0.4)– +15 µm +. + + + +TABLE 4. +Spicule measurements of + +Petrosia +( +Petrosia +) +revizee + + +sp. nov. + +Values given as min.-–med. (SD)–max, in µm. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
SpecimensOxea (length/ width)
Holotype MNRJ 22190 (Bahia)I: 102–165 (30)–218/ 5–7 (3)–10 II: 48–66 (14)–97/ 5–8 (3)–15
Bahia, Paratypes MNRJ 2652I: 145–188 (14.5)–208/ 5–9 (2.2)–15 II: 44–76 (10.1)–92/ 5–5 (0)–5
MNRJ 3274AI: 121–184 (22.3)–223/ 5–5 (0)–5 II: 48–56 (5.5)–73/ 5–5 (0)–5
MNRJ 4461I: 116–164 (24.4)–203/ 5–5 (0)–5 II: 39–54 (8.4)–73/ 5–5 (0)–5
MNRJ 4675I: 116–177 (18.5)–208/ 5–5 (0)–5 II: 53–73 (10.3)–92/ 5–5 (0)–5
MNRJ 4793I: 150–208 (21.7)–247/ 5–5 (0)–5 II: 53–68 (11.1)–92/ 5–5 (0)–5
MNRJ 4851I: 126–194 (31)–242/ 5–5 (0)–5 II: 48–68 (9.9)–80/ 5–5 (0)–5
MNRJ 4897I: 169–233 (23.7)–266/ 5–10 (2.6)–15 II: 48–70 (12.5)–92/ 5–5 (0)–5
MNRJ 10575I: 150–213 (19.8)–252/ 5–9 (1.5)–10 II: 53–78 (7.5)–92/ 5–5 (0)–5
MNRJ 13119I: 145–204 (15)–232/ 5–8 (2.3)–10 II: 48–72 (11.5)–92/ 5–5 (0)–5
UFRJPOR 4043I: 150–209 (23.8)–247/ 5–9 (1.9)–10 II: 39–75 (15.2)–91/ 5–5 (1)–5
MNRJ 17022I: 155–222 (22.8)–257/ 5–10 (2.2)–15 II: 44–80 (13.7)–97/ 5–5 (1)–10
MNRJ 3117BI: 116–174 (17.3)–203/ 5–5 (0)–5 II: 39–56 (7.7)–77/ 5–5 (0)–5
+
+ +......continued on the next page + +
+ + +TABLE 4. (Continued) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Specimens
MNRJ 3225A
Additional material
Espírito Santo
MNRJ 4672
MNRJ 4882
MNRJ 4928
MNRJ 4948
MNRJ 5020
MNRJ 6572
MNRJ 6574
off Rio de Janeiro
MNRJ 5981
MNRJ 5973C
MNRJ 6595
+ + + +Ecology. + +Petrosia +( +P. +) +revizee + + +sp. nov. + +occurs at +16–270 m +depth, over rhodolith beds, corals, mud and gravel bottoms. +Paratype +MNRJ 2652 showed associated cirripeds, ophiuroids and algae. + + + + +Etymology. +The specific epithet is used as a noun in apposition, and recognizes the importance of Program REVIZEE, promoted by the Brazilian government to assess the sustainable catch limits in the country’s Exclusive Economic Zone. Thousands of sponge samples were deposited in the MNRJ collection then, mostly dredged and trawled on the country’s continental shelf and slope. + + + + +Type locality. + +Hotspur Seamount +, off +Bahia State +. +Additional distribution. +Provisional Brazilian +endemic, so far known from the +States +of +Pernambuco +(depth not recorded), +Alagoas +( + +18 m + +) + +, + +Bahia +( + +15.8–67 m + +) + +, + +Espírito Santo +( + +50–85 m + +) + + +and off +Rio de Janeiro +( + +270 m + +) + +. + + +Taxonomic Remarks. +There are five species of + +Petrosia +( +Petrosia +) + +known in the Western Tropical Atlantic ( +Table 5 +). None of these has two, and only two well-differentiated categories of oxeas, being also devoid of any microsclere categories. + + +Given the current state of flux in haplosclerid classification, where departure from monospecificity often implies polyphyletism, we found it appropriate to compare this new species in particular, with + +Neopetrosia proxima + +, as both share some morphological traits which initially misguided our identification. Both genera are supposed to have distinct ectosomal architectures—“They differ especially in their ectosomal skeleton and the size categories of their spicules” ( +Desqueyroux-Faúndez & Valentine 2002 +)—but overall, the images illustrating the ectosomes of + +N. proxima + +( +Figs 2C–D +) and of + +P. +( +P. +) +revizee + + +sp. nov. + +( +Fig. 4C +) bear a remarkable resemblance. In order to match the diagnosis for + +Neopetrosia + +ectosomes, architectures should bear fine brushes of oxeas issued from subectosomal tracts, a remark that does not easily contrast to what is said about + +Petrosia + +, namely, that their ectosome should bear a triangular or polygonal reticulation of spicule tracts or single spicules, usually echinated at the nodes or along the tracts by a smaller category of spicules. In case of doubt, one usually resorts to an identification key, and Des- + + + +TABLE 5. +Comparative morphological data for + +Petrosia (Petrosia) + +spp. from the Western Tropical Atlantic. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Species +H. += habitus; +S. += surface; +Cv. += Color +in vivo +; +Cs. += consistency; +O. += oscules; +E. += ectosome; +Ch. += choanosome + +Spicules + +Locality/ Depth +
+Oxeas I: +102–208–305/ 5–7–15 µm +
+Oxeas II: +39–71–97/ 5–5–10 µm +
+ + +P. +( +P. +) +revizee + +sp. nov. + + +H. +mass./ ramose, lobate; +S. +smooth, irreg.; +Cv. +pink, red-wine, white; +Cs. +hard, incompress./ slightly compress., friable; +O. +circ. (1–4 mm diam.), scatt. on surf., leveled/ slight. raised; +E. +retic. w. rounded meshes; +Ch. +retic. w. ovate/ rectang. meshes +Bahia, Espírito Santo and Rio de Janeiro States/ 16–270 m
+ + +P. +( +P. +) +cretacea +( +Schmidt, 1870 +) + + +(orig. descr.) +incertae sedis +in WPD + +H. +several inches thick, about 23 cm wide, flat; +S. +irreg. undul., nodular; +Cv. +n.r.; +Cs. +softer than + +Cribrochalina vasculum + +(as + +C. infundibulum + +); +O. +n.r.; +E. +n.r.; +Ch. +in between chalinid and +P. (P.) +architec. + +Oxeas: +146 µm +Florida State, USA/ n.r.
+Strongyles +: 60–435/7–17 µm +Styles +: 270–440/3–14 µm +
+ + +P. ( +P. +) +incrustata +Alcolado & Gotera + +, + + +H. +thin. crust., lobate; +S. +n.r.; +Cv. +violet-brown ext., beige int.; +Cs. +
+1986 + +very smooth, fragile, fleshy; +O. +apical on lobes, 3 mm diam.; +E. +Cuba/ 30 m
(orig. descr.) +n.r.; +Ch. +loose, w/ thin spong. fibers part./ total. filled by spics. +
+
+ +......continued on the next page ......continued on the next page +queyroux-Faúndez & Valentine’s (2002) happens to contrast + +Neopetrosia + +and +P. +( + +Petrosia + +) in terms slightly different from those presented in both (sub)genera’s diagnoses. The ectosome of the former is classified as a tangential network with isodictyal meshes of single spicules, and free spicules at the nodal points, and that of the latter, as a tangential network with rounded regular meshes and free spicules. The main difference as far as the ectosome goes rests on the possession of isodictyal vs rounded meshes respectively. It seems, nevertheless, that the sorting of + +Neopetrosia + +is resting too much on the unispicular isodictyal reticulation of its +type +species, and not accounting for the variability exhibited in additional species assigned to this genus, as outlined by + +Santos +et al. +(2016) + +. Given this rationale, we have opted to focus on the new species’ possession of two clearly distinguishable categories of oxeas, and in the fact that the smaller of these appears to be preferably echinating the bundles, to justify its assignment to + +Petrosia + +instead of + +Neopetrosia + +. In spite of both species referred to above possessing similar ectosomal architectures, they can be easily distinguished on the basis of spicule morphology, categories and arrangement. Therefore, we feel confident that + +P. +( +P. +) +revizee + + +sp. nov +. + +is indeed a new species. + +
+
+
\ No newline at end of file diff --git a/data/38/5D/D7/385DD759B56B10AE7F7852798E92327D.xml b/data/38/5D/D7/385DD759B56B10AE7F7852798E92327D.xml new file mode 100644 index 00000000000..0302d4102b7 --- /dev/null +++ b/data/38/5D/D7/385DD759B56B10AE7F7852798E92327D.xml @@ -0,0 +1,89 @@ + + + +Checklist of British and Irish Hymenoptera - aculeates (Apoidea, Chrysidoidea and Vespoidea) + + + +Author + +Else, George R. + + + +Author + +Bolton, Barry + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8050 +8050 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8050 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8050 +1314-2828--8050 + + + + + +Myrmica karavajevi ( +Arnol'di +, 1930) + + + + + +Symbiomyrma karavajevi +Arnol'di +, 1930 + + +laurae +misident. + + +pechei +(Samsinak, 1957, +Sifolinia +) + + +faniensis +van Boven, 1970 + + +winterae +(Kutter, 1973, +Sifolinia +) + + + +Distribution +England, Wales + + + \ No newline at end of file diff --git a/data/38/5E/0F/385E0F22EA0DD71B814756BFD0325122.xml b/data/38/5E/0F/385E0F22EA0DD71B814756BFD0325122.xml new file mode 100644 index 00000000000..263cc111469 --- /dev/null +++ b/data/38/5E/0F/385E0F22EA0DD71B814756BFD0325122.xml @@ -0,0 +1,176 @@ + + + +Flora der Schweiz und angrenzender Gebiete. Band 1. Pteridophyta bis Caryophyllaceae (2 nd edition): Registerzuband 1 + + + +Author + +Hess, Hans Ernst + + + +Author + +Landolt, Elias + + + +Author + +Hirzel, Rosmarie + +text + +1972 +Birkhaeuser Verlag + + +https://doi.org/10.5281/zenodo.291815 + +book +291815 +10.5281/zenodo.291815 +3-7643-0843-5 + + + +<subSubSection id="E198C2AB50A1B7B25DFFF47010E8B326" pageId="null" pageNumber="450" type="nomenclature"> +<paragraph id="258AFB3730D73AE920F8AA093258A2EF" pageId="null" pageNumber="450"> +<taxonomicName id="8EBFA46B6E2FB6D5B3801377BF5FBEF6" ID-CoL="7DHLW" authority="L." class="Liliopsida" family="Cyperaceae" genus="Carex" kingdom="Plantae" order="Poales" pageId="null" pageNumber="450" phylum="Tracheophyta" rank="species" species="caespitosa"> +Carex +<normalizedToken id="CA1EEBD56DFF43D836F45AA79BC3ADE7" originalValue="caespitósa" pageId="null" pageNumber="450">caespitosa</normalizedToken> +L. +</taxonomicName> +</paragraph> +</subSubSection> +<subSubSection id="7DAFB12770B16AC5FAD409C0A8E57CF2" pageId="null" pageNumber="450" type="vernacular_names"> +<paragraph id="535C16B04D48AC3DD1C2FEFBE64F220D" pageId="null" pageNumber="450">Horstbildende Segge</paragraph> +</subSubSection> + + + +20-60 cm hoch; horstbildend. + +Grundstaendige +, blattlose Scheiden rotbraun, +glaenzend +, nicht gekielt, zahlreich + +(meist +ueber +5), + +viel kleiner als bei +C. elata + +(Nr. 46); +blaettertragende +Scheiden gelbbraun; alle Scheiden +ohne Gitternerven. +Blaetter +1,5-3 mm breit, flach, steif, +gruen +, den +Bluetenstand +nicht erreichend. Stengel aufrecht, scharf 3kantig, +duenner +als bei + +C. elata + +( +Seitenlaenge +<1 mm), rauh. +Bluetenstand +wie bei + +C. elata + +, die + +Aehren +aber nur 0,5-2 cm lang. Meist alle +Hochblaetter +den +Tragblaettern +aehnlich +, gelegentlich +Hochblaetter +der untersten +Aehre +blattaehnlich +, aber +kuerzer +als diese +Aehre +. + +Tragblaetter +wie bei + +C. elata +. + +Fruchtschlaeuche +2-2,5 mm lang, in der Mitte am breitesten (1-1,5 mm), Form und +Oberflaeche +wie bei + +C. elata +, jedoch ohne Nerven; + +Narben 2. + + +Zytologische Angaben. 2n = 80: +Material aus Schweden (Heilborn 1922Heilborn 1924), ohne Herkunftsangabe (Davies 1956a). + + +Standort. +Kollin. Nasse, torfige, meist kalkfreie +Boeden +. Kleinseggen- und +Grossseggengesellschaften +. + + +Verbreitung. Eurasiatische Pflanze: +Nord-, Mittel- und Osteuropa, Sibirien (bis Baikalseegebiet), Zentralasien. - Im Gebiet: +Dep +. Jura, +Dep +. Doubs (westlich Pontarlier), +Elsass +, Baden (wenige Fundstellen), Angaben aus Jura und Mittelland z.T. unsicher (eindeutige Belege im Herbar der ETH: Meienmoos bei Burgdorf), Aostatal (Valchiusella); Angaben aus dem Veltlin beziehen sich wahrscheinlich auf + +C. elata + +(Nr. 46). + + +Bemerkungen. +Die Verbreitung von + +C. caespitosa + +ist im Gebiet festzustellen. Die Art ist an den nervenlosen +Fruchtschlaeuchen +leicht von den nahe verwandten Arten zu unterscheiden; zudem sollen sich nach +Hoeller +(1964) bei + +C. caespitosa + +die +Blaetter +beim Trocknen stets nach unten einrollen (bei + +C. fusca + +stets nach oben), was besonders am untersten Hochblatt deutlich zu sehen sein soll. + + + + \ No newline at end of file diff --git a/data/38/5E/70/385E70072519591CA2BDB2A4BA7AEECA.xml b/data/38/5E/70/385E70072519591CA2BDB2A4BA7AEECA.xml new file mode 100644 index 00000000000..258a85d057d --- /dev/null +++ b/data/38/5E/70/385E70072519591CA2BDB2A4BA7AEECA.xml @@ -0,0 +1,129 @@ + + + +New records of eumenine wasps (Hymenoptera, Vespidae, Eumeninae) from Russia, with description of a new species of Stenodynerus de Saussure, 1863 + + + +Author + +Fateryga, Alexander V. +https://orcid.org/0000-0002-5346-3477 +T. I. Vyazemsky Karadag Scientific Station - Nature Reserve of RAS - Branch of A. O. Kovalevsky Institute of Biology of the Southern Seas of RAS, Kurortnoye 298188, Feodosiya, Russia + + + +Author + +Proshchalykin, Maxim Yu. +https://orcid.org/0000-0001-7870-8226 +Federal Scientific Center of the East Asia Terrestrial Biodiversity, Far East Branch of the Russian Academy of Sciences, Vladivostok 690022, Russia +proshchalikin@biosoil.ru + + + +Author + +Kochetkov, Denis N. +Khingan State Nature Reserve, Arkhara 676740, Russia + + + +Author + +Buyanjargal, Batchuluun +Institute of General and Experimental Biology, Mongolian Academy of Sciences, Ulaanbaatar 210351, Mongolia + +text + + +Journal of Hymenoptera Research + + +2020 + +2020-10-30 + + +79 + + +89 +109 + + + + +http://dx.doi.org/10.3897/jhr.79.57887 + +journal article +http://dx.doi.org/10.3897/jhr.79.57887 +1314-2607-79-89 +2C9F2068B7084AF492B41AA28B2070A3 +AF268A9D9FF15BD4830480B83E0854A0 +4255483 + + + + + +Stenodynerus orenburgensis ( +Andre +, 1884) + + + + + +Figures 23 +, 50-54 + + + +Material examined. + + +Russia +: + +Khakassia + +, +Altayskiy Distr. +, +Izykhskiye Kopi +, +53°30.43'N +, +91°13.11'E +, +13.VI.2012 +, ( +1 ♀ +), leg. MP, VL [CAFK]; +Shira Distr. +, Chernoye Ozero, +Chernoye Lake +, +54°39.04'N +, +89°23.23'E +, +16.VII.2012 +, ( +1 ♂ +), leg. MP, VL [CAFK] + +. + + + +Distribution. + +Russia: European part (Central, South, North Caucasus, Crimea), Urals, Western Siberia (Omsk Prov., Altai), Eastern Siberia (* +Khakassia +, Irkutsk Prov., Buryatia, Zabaikalskiy Terr.). - Europe, Caucasus, Turkey, Kyrgyzstan, Kazakhstan, Mongolia, China. + + + + \ No newline at end of file diff --git a/data/38/5E/B0/385EB0930BEC1F48D8D76A2F8F1800F2.xml b/data/38/5E/B0/385EB0930BEC1F48D8D76A2F8F1800F2.xml new file mode 100644 index 00000000000..77613d22680 --- /dev/null +++ b/data/38/5E/B0/385EB0930BEC1F48D8D76A2F8F1800F2.xml @@ -0,0 +1,56 @@ + + + +Marine Bryozoa of Greece: an annotated checklist + + + +Author + +Gerovasileiou, Vasilis + + + +Author + +Rosso, Antonietta + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +10672 +10672 + + + + +http://dx.doi.org/10.3897/BDJ.4.e10672 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e10672 +1314-2828-4-10672 + + + + +Victorella pavida Saville-Kent, 1870 + + + +Notes + +Castritsi-Catharios et al. 1986a +, +Castritsi-Catharios et al. 1986b + + + + \ No newline at end of file diff --git a/data/38/5F/2E/385F2EDD003DAC2C2F1A32C5DBDDC791.xml b/data/38/5F/2E/385F2EDD003DAC2C2F1A32C5DBDDC791.xml new file mode 100644 index 00000000000..fa987160656 --- /dev/null +++ b/data/38/5F/2E/385F2EDD003DAC2C2F1A32C5DBDDC791.xml @@ -0,0 +1,143 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828-4-9042 + + + + +Eutanyacra glaucatoria (Fabricius, 1793) + + + + +Ichneumon glaucatorius +Fabricius, 1793 + + +Eutanyacra glaucatoria +? +albiventris +(Gmelin, 1790, +Ichneumon +) + + +hungarica +(Tischbein, 1868, +Amblyteles +) + + +sicula +(Rudow, 1888, +Amblyteles +) + + +distyca +(Berthoumieu, 1894, +Amblyteles +) + + +hispanica +(Berthoumieu, 1896, +Amblyteles +) + + +spoliata +(Berthoumieu, 1896, +Amblyteles +) unavailable + + +medinai +(Berthoumieu, 1903, +Amblyteles +) + + +nigroscutellatus +(Ulbricht, 1909, +Amblyteles +) preocc., unavailable + + +praetexta +(Berthoumieu, 1910, +Amblyteles +) + + +bruyanti +(Pic, 1927, +Amblyteles +) + + +viturati +(Pic, 1927, +Amblyteles +) + + +krapinensis +(Schmiedeknecht, 1930, +Amblyteles +) + + +bimaculata +(Constantineanu, 1954, +Amblyteles +) preocc. + + + +Distribution +England, Ireland + + +Notes + +Eutanyacra ruficornis +(Berthoumieu, 1894, +Eurylabus +) was removed from synonymy by +Horstmann (2006c) +. + + + + \ No newline at end of file diff --git a/data/38/5F/88/385F88BA885F36049BC1D7856AAEDDB7.xml b/data/38/5F/88/385F88BA885F36049BC1D7856AAEDDB7.xml new file mode 100644 index 00000000000..6344f8e374b --- /dev/null +++ b/data/38/5F/88/385F88BA885F36049BC1D7856AAEDDB7.xml @@ -0,0 +1,71 @@ + + + +A survey of the family Carabodidae C. L. Koch, 1836 (Acari: Oribatida), II + + + +Author + +Mahunka, S. + +text + + +Acta Zoologica Hungarica + + +1987 + +33 + + +399 +434 + + + + +http://unknown + +journal article +ORI5672 + + + + + +Guineobodes + +gen. n. + + + + +Diagnosis: Family +Carabodidae +, subfamily: +Opisthocepheinae +. Lamellae fused medially, translamellar apophysis, convex dorsosejugal region and a very highly notogastral elevation present. Fourteen pairs of notogastral setae. Epimeral setal formula: 3 +-1-3- +3. Anogenital setal formula: 5- 1 +-2- +3. + + + + +Type-species: +Machadocepheus papuanus +Balogh, 1970. + + + + +Remarks: The new genus stands very near to +Opisthocepheus +Aoki, 1977, however, the latter has only four pairs of genital setae, one pair of the notogastral setae in humeral position, and its interlamellar setae short and arising on the surface of the translamellar apophysis. + + + + \ No newline at end of file diff --git a/data/38/5F/BE/385FBECB08663C4BEEE012E7CD2C509B.xml b/data/38/5F/BE/385FBECB08663C4BEEE012E7CD2C509B.xml new file mode 100644 index 00000000000..40d0ce9708d --- /dev/null +++ b/data/38/5F/BE/385FBECB08663C4BEEE012E7CD2C509B.xml @@ -0,0 +1,327 @@ + + + +Phylogeny of the genus Yumtaax Boucher (Coleoptera, Passalidae, Proculini): Taxonomic and evolutionary implications with descriptions of three new species + + + +Author + +Beza-Beza, Cristian Fernando + + + +Author + +Beck, James + + + +Author + +Reyes-Castillo, Pedro + + + +Author + +Jameson, Mary Liz + +text + + +ZooKeys + + +2017 + +667 + + +95 +129 + + + + +http://dx.doi.org/10.3897/zookeys.667.10716 + +journal article +http://dx.doi.org/10.3897/zookeys.667.10716 +1313-2970-667-95 +648D539FD99443188CD23F183172350C +648D539FD99443188CD23F183172350C + + + + +Yumtaax jimenezi Beza-Beza, Reyes-Castillo & Jameson +sp. n. + + + +Material examined. +27 type specimens. + +Holotype ♂. MEXICO: Veracruz, Calcahualco, Tecuanapa. Bosque +mesofilo +, alt. 2400 m V-2/3-1992 ( +Capistran +and Delgado) (IEXA). + + +Paratypes (26 total). MEXICO: Veracruz: 10 ♀, 15 unknown sex, Calcahualco, Tecuanapa, bosque +mesofilo +, alt. 2400 m, V-2/3-1992 ( +Capistran +and Delgado). 5 ♂, 8 ♀, 34 sex unknown, Calcahualco, Tecuanapa, bosque +mesofilo +, alt. 2400 m, V-1992 ( +Capistran +and Delgado). 14 ♀, Calcahualco, Tecuanapa, bosque +mesofilo +, alt. 2200 m, VI-1992 ( +Capistran +and Delgado). 1 ♂, Calcahualco, Dos Caminos, II-29-1992, alt. 1415 m, bosque de encino-pino, dentro de +Quercus +sp. (R. Novelo, F. +Capistran +and L. Delgado). 1 ♀, 2 sex unknown, Calcahualco, Nueva +Vaqueria +(1 km before), II-28-1992, alt. 2700 m, bosque de pino-encino, en tronco (R. Novelo, F. +Capistran +and L. Delgado). 2 ♀, Veracruz, Calcahualco, 1 km antes de Nueva +Vaqueria +, 2700 m, VI-1992, (L. Delgado and +Capistran +) (CFBB, IEXA). 1 ♂, Cosautlan, Los Laureles, alt. 2680 m, VIII-27-1999 (J. P. Lumaret). 4 sex unknown, Orizaba, +Salle +, Mex. Collection ( +Salle +) (BMNH). 1 sex unknown, Mexico (Truqui) (BMNH). + + + +Diagnosis. + +Yumtaax jimenezi +is a small (18.5-23.0 mm) macropterous species, and it is part of the +Y. laticornis +clade (=Fig. 4). This species is diagnosed by the following character combination: clypeus is inclined (shared with +Y. recticornis +, +Y. imbellis +, +Y. mazatecus +, +Y. nebulosus +, +Y. olmecae +; vertical in +Y. laticornis +, +Y. cameliae +, +Y. veracrucensis +) and with the anterior border straight (shared with other members of +Yumtaax +except for +Y. recticornis +and +Y. olmecae +that have the anterior border of clypeus concave); MFS of the +"falsus" +type (see +Reyes-Castillo 1970 +) (shared with all members of +Yumtaax +except +Y. cameliae +which has the MFS of the +"striatopunctatus" +type), with the central tooth that is not free (fused with frontal ridges) (shared with +Y. imbellis +, +Y. nebulosus +, +Y. olmecae +; largely free in +Y. recticornis +, +Y. veracrucensis +, +Y. laticornis +, +Y. cameliae +, +Y. mazatecus +), directed dorsally and anteriorly (shared with +Y. mazatecus +, directed dorsally +Y. recticornis +, +Y. imbellis +, +Y. nebulosus +, +Y. olmecae +; directed anteriorly in +Y. veracrucensis +, +Y. laticornis +; elevated in the posterior half bending abruptly forward in the anterior half in +Y. cameliae +), and not reaching the clypeus (shared with +Y. recticornis +, +Y. imbellis +, +Y. mazatecus +, +Y. nebulosus +, +Y. olmecae +; reaching the clypeus in +Y. laticornis +, +Y. cameliae +, +Y. veracrucensis +); and moderately reduced eyes (shared with +Y. veracrucensis +, +Y. cameliae +, +Y. nebulosus +, +Y. olmecae +; large in +Y. recticornis +, +Y. imbellis +; strongly reduced in +Y. laticornis +, +Y. mazatecus +). + + + + +Dimensions + + +(mm) (n = 12). Total length 18.5-23.0, ( +x += 20.5); elytral length 11.5-14.0, ( +x += 12.5); pronotal length 4.0-6.0, ( +x += 5.5); pronotal width 5.5-7.0, ( +x += 6.5); humeral width 5.5-7.0, ( +x += 6.5). + + + +Description of holotype + +(Fig. 9). Head (Fig. 9C). Labrum: anterior border concave, dorsal surface smooth and glabrous medially, and punctate and setose in the apicolaterally, apically, and basally; anterior edge excavated. Clypeus: inclined, rectangular, shiny, and smooth. Frontoclypeal suture: straight, and shiny. External tubercles rounded and directed dorsally. Frontal area: inclined, smooth, and shiny, frontal ridges present finishing in inner tubercles. Frontal fossae: punctate and setose. Mesofrontal +structure +(MFS): of the +"falsus" +type (see +Reyes-Castillo 1970 +); base subparallel and narrower than the +MFS' +lateral ridge; center horn short with apex rounded, not free (fused with frontal ridges) and directing dorsally (Fig. 9D), not reaching the posterior margin of clypeus (Fig. 9C, D), dorsally without micro-punctures; base of the center horn narrow not narrowing down along its length (central tooth tubercle like shape [Fig. 9C, D]); dorsal fossa present at the base of MFS. Occipital fossa: shallow posteriorly and deeper laterally not connected to frontal fossae. Posterior occipital sulcus sinuate. Supraorbital ridge: bituberculate, tubercles of similar size; posterior half of supraorbital ridge not bifurcated. Canthus: with apex rounded covering less than 1/3 of the eye, expanded distally. Eyes: reduced (distal edge of the eye more or less at the distal edge of the canthus), width = 0.5 mm (each eye). Head width = 3.5 mm. Ratio of sums of both eyes widths/total head width = 0.24; postocular area punctate and setose. Ligula: tridentate, with central tooth surpassing apex of lateral teeth, lateral teeth rounded; setose punctures present in discal area; posterior border convex. Mentum: lateral lobes rounded and wide, with setose punctures. Basomedial portion protruding ventrally; anterior border at middle convex; basal fossae absent. Hypostomal process: without lateral depression; separated from mentum by a distance shorter than the wide of the anterior width of hypostomal process. Infraocular ridge absent. Mandible: with 3 apical teeth; internal tooth of left mandible bidentate; dorsal tooth occupies less than half length of the mandible. Pronotum: anterior angles rounded. Anterior fossae of marginal sulcus impunctate. Lateral fossae with heavy punctures. Marginal groove lacking punctures. Prosternum: opaque. Prosternellum anterior half opaque and lateral edges and posterior half shiny. Scutellum: smooth and glabrous. Mesosternum: with anterolateral areas opaque. Metasternum: with setae in anterolaterally, without punctures in lateral margins of metasternum disc. Lateral fossae wide across the metathorax, with setose punctures. Elytra: anterior border straight. Meeting point of striae 1-10 (see +Reyes-Castillo 1970 +) with one line of punctures. Wings: well developed. Legs: femur I with longitudinal anteroventral groove weakly developed in the proximal half and strongly developed on the distal end of the femur, posteroventral half pubescent; setae long, sparse, reddish. Abdomen: last sternite with marginal groove complete (Fig. 9B). Aedeagus (Fig. 9E, F, G): in dorsal view phallus globose (wider than long). In ventral view distal edges of phallus surpassing the distal edge of the parameres. + + + +Variation. +Frontoclypeal suture can be from opaque to shiny; internal tubercles from strongly to weakly marked but always present; ratio of eyes and head with varies from 0.18-0.32; supraocular ridge from weak to absent; hypostomal process with weak lateral depression to lateral depression absent; prosternellum varies from anterior half opaque and lateral edges and posterior half shiny to anterior half and lateral edges opaque and posterior half and middle shiny to completely opaque; femur I longitudinal anterior-ventral groove from weak in the proximal half to absent; femur I longitudinal anterior-ventral groove from strongly developed in the distal half to absent. + + +Etymology. + +This species is named in honor of +Passalidae +worker Dr. Larry +Jimenez-Ferbans +who assisted in collecting trips supporting this study. + + + + +Distribution +. + + +This species is known from cloud forest (bosque +mesofilo +) at 2400 m elevation from the state of Veracruz, Mexico. + + +MEXICO: Veracruz: Calcahualco (Tecuanapa, Dos Caminos, Nueva +Vaqueria +[1 km before]). + + + +Remarks. + +Yumtaax jimenezi +is a cryptic, widespread species that has been confused with +Y. recticornis +. Previously, +Y. recticornis +s. l. was thought to be broadly distributed in Mexico from the Sierra Madre Oriental in the Mexican Transvolcanic Belt and Sierra Madre del Sur ( +Reyes-Castillo 1970 +, +Castillo and Reyes-Castillo 1984 +, +Boucher 2006 +). Phylogenetic analysis (Fig. 4 and Suppl. materials 2-4) and close examination of morphology provide evidence that +Y. recticornis +s. l. comprises two cryptic species [ +Y. recticornis +(= +Y. recticornis +OM) and +Y. jimenezi +( +Y. recticornis +VM)]. + + +These species are distinguished by eye size (small in +Y. jimenezi +and large in +Y. recticornis +), shape of the central tooth of the MFS (center horn short with apex rounded, not free [fused with frontal ridges] and directed dorsally [Fig. 9D] in +Y. jimenezi +; center horn short with apex rounded, largely free and directed anteriorly and dorsally [Fig. 5D] in +Y. recticornis +), and the shape of the surface of the frons and clypeus (concave in +Y. recticornis +versus flat in +Y. jimenezi +). Interestingly, the reduced eye size in +Y. jimenezi +results in the distal expansion of the canthus. Based on seven exemplars, phylogenetic analysis (Fig. 4) strongly supports +Y. jimenezi +as a unique lineage (1.0 PP/100 BS). + + + +Figure 9. +Yumtaax jimenezi +Beza-Beza, Reyes-Castillo & Jameson, sp. n., holotype: A dorsal habitus B ventral habitus C dorsal view of pronotum and head D lateral view of pronotum and head E lateral view of aedeagus F ventral view of aedeagus G dorsal view of aedeagus. + + + + + \ No newline at end of file diff --git a/data/38/60/33/38603375FF82E532159BFAEDFB12F86E.xml b/data/38/60/33/38603375FF82E532159BFAEDFB12F86E.xml new file mode 100644 index 00000000000..2787dd9f35d --- /dev/null +++ b/data/38/60/33/38603375FF82E532159BFAEDFB12F86E.xml @@ -0,0 +1,185 @@ + + + +A review of the genus Mirocastnia J. Y. Miller, 1980 (Lepidoptera: Castniidae) with records of recently collected specimens + + + +Author + +González, Jorge M. +0000-0001-7208-7166 +gonzalez.jorge.m@gmail.com + + + +Author + +Thöny, Hubert +Reserva Serra Bonita, P. O. Box 1, Cep 45.880 - 000 Camacan / Bahia, Brasil + + + +Author + +Worthy, Robert +10 The Hill, Church Hill, Caterham, Surrey CR 3 6 SD, U. K. + +text + + +Zootaxa + + +2024 + +2024-02-29 + + +5418 + + +3 + + +240 +254 + + + + +http://dx.doi.org/10.11646/zootaxa.5418.3.3 + +journal article +290084 +10.11646/zootaxa.5418.3.3 +9db943bf-b712-4874-9788-25c275bb2168 +1175-5326 +10726400 +E2B67801-0FEA-4D03-84C8-38884A925A3A + + + + + + + +subcoerulea +( +Rothschild, 1919 +) + + + + + + + +“ + +Castnia (Schaefferia) subcoerulea + +, + +sp. nov. + +” +Rothschild, 1919 +: +Novitates zoologicae +26 +(1): 18. ( +Figs. 2G, H +). + + + + +Type material: +Described from a single female which is the holotype by monotypy ( +Figs. 2G, H +). This holotype was in the collection of Lionel Walter Rothschild (1868–1937), it is now in +NHMUK +. + + +Type locality: +Rothschild (1919) +only gave the type locality as +Ecuador +, and this is all that is mentioned on the label data of the specimen. This cannot now be further restricted. + + +Taxonomic status: +A junior subjective synonym of + +M. pyrrhopygoides +( +Houlbert, 1917 +) + +. Originally described as a species in the genus + +Castnia +( +Schaefferia +) + +, it was synonymised with + +M. pyrrhopygoides + +by +Miller (1980) +. + + +Male genitalia +: Not relevant. + + + + +Distribution: +Not relevant. + + + + +Discussion: +Houlbert (1917) +described + +M. pyrrhopygoides + +from +three males +; Rothschild’s + +subcoerulea + +was the first description of the female, which is quite different from the male and was not at the time recognised as being the same species; this problem was exacerbated by the fact that the male and female were placed in different genera by their authors. +Miller (1980) +was the first to recognise their conspecificity. + + + + +Material examined: + +For this study we have examined the +holotype +. + +HT subcoerulea 1919 R[othschild], +Ecuad[or] +, 339., Joicey Bequest. Brit. Mus., +NHMUK010305386 +, vial +NHMUK010402734 + +. + + + + \ No newline at end of file diff --git a/data/38/60/33/38603375FF85E535159BFF41FD6CF892.xml b/data/38/60/33/38603375FF85E535159BFF41FD6CF892.xml new file mode 100644 index 00000000000..4c3943de49e --- /dev/null +++ b/data/38/60/33/38603375FF85E535159BFF41FD6CF892.xml @@ -0,0 +1,503 @@ + + + +A review of the genus Mirocastnia J. Y. Miller, 1980 (Lepidoptera: Castniidae) with records of recently collected specimens + + + +Author + +González, Jorge M. +0000-0001-7208-7166 +gonzalez.jorge.m@gmail.com + + + +Author + +Thöny, Hubert +Reserva Serra Bonita, P. O. Box 1, Cep 45.880 - 000 Camacan / Bahia, Brasil + + + +Author + +Worthy, Robert +10 The Hill, Church Hill, Caterham, Surrey CR 3 6 SD, U. K. + +text + + +Zootaxa + + +2024 + +2024-02-29 + + +5418 + + +3 + + +240 +254 + + + + +http://dx.doi.org/10.11646/zootaxa.5418.3.3 + +journal article +10.11646/zootaxa.5418.3.3 +1175-5326 +10726400 +E2B67801-0FEA-4D03-84C8-38884A925A3A + + + + + + + +smalli +J.Y. +Miller, 1980 + + + + + + + +“ + +Mirocastnia smalli + +, +new species +” J. Y. +Miller, 1980 +: +Bulletin of the Allyn Museum +60 +: 11–14, figs. ( +Fig. 1 +). + + + + +Type material: +Described from a male +holotype +( +Figs. 1A, B +), +six male +and +four female +paratypes +, all the types are in +MGCL +( +González, 2023 +). The type series was collected by Gordon B. Small Jr. ( +Miller, 1980 +). + + +Type locality: + +The +holotype +was collected at +Cerro Jefe +, a mountain in +Panama province +, +Panama +, just south of the +Chagres National Park + +. + + +Taxonomic status: +A subspecies of + +M. pyrrhopygoides +( +Houlbert, 1917 +) + + +stat. nov. + +This is the +type +species of the genus, also listed in this combination by +Miller (1995) +and +Lamas (1995) +. + + +Male genitalia: +(Fig, 7F, G) Genital capsule with a single uncus, socii are slightly developed. Gnathos bifurcate. Valva elongate along the costal margin. A pronounced recurved cleft is present by the sacculus. Saccus is reduced. Juxta is moderately sclerotised.The aedeagus is slightly curved, barely recurved, moderately sclerotised. It possesses a dorsal sclerotised plate. + + + + +Distribution: +This subspecies is found in +Panama +, currently known from +Chiriquí +, +Coclé +and +Panamá +provinces. A specimen was recently reported to us which was found in +Guanacaste province +in the north-west of +Costa Rica +( +Fig. 1E, F +), it was collected whilst flying on the top of Volcán Orosí. The specimen was apparently hilltopping and was caught by hand. This is the northernmost known specimen in the genus, the first record for +Costa Rica +and a major range extension for the species ( +Fig. 5 +). + + + + +Discussion: +The overall appearance of this subspecies is darker and smaller than + +M. p. +pyrrhopygoides + +. The male is especially dark along the tornus of the hindwing on both surfaces. The two pairs of pale postdiscal spots are also more contrasted in + +smalli + +than in + +pyrrhopygoides + +. In the female, the blue patch on the hindwing is even more reduced than it is in + +pyrrhopygoides + +on both surfaces. In both sexes, the forewing transverse semi-hyaline band seems to be slightly wider than in + +pyrrhopygoides + +. However, these features are variable in all subspecies so are merely an average. Much more material of + +Mirocastnia + +is known now than was available to Miller when she wrote her 1980 paper, which shows that the features she selected to separate her species do not always hold true in longer series. + +The subspecies was named after its discoverer, Gordon Burgess Small, Jr. (1934–1989). + + + +Material examined: + +8 males +and +5 females +were examined for this study: PANAMA: + +HT +Panamá +, +Cerro Jefe +, ca. + +900m +. + +, + +11.iii.1977 + +, +G.B. Small +/ 111078 6,7, Gordon Small Collection, MGCL/FLMNH Specimen no. 47927, UF +FLMNH +, +MGCL 1138161 + +; + +1♀ +PT Panama, +Panama +, +Cerro Jefe +, + +900m + +, + +11.iii.1977 + +G.B. Small +, genitalia vial no. M-3802 Jacqueline Y. Miller, Allyn Museum Acc. 1977-14, +UF +FLMNH +MGCL 1138203 + +; + +1♀ +PT +Panama +, +Pma +, +Cerro Campana +, 2500’, + +2vii70 + +Coll. G. B. Small +, 111078 8,9, Gordon B. Small Collection, Allyn Museum photo No. 091076-2/3, genitalia vial no. M-3640 Jacqueline Y. Miller, UF +FLMNH +MGCL 1138199 + +; + +1♀ +PT Panama, +Panama +, +Cerro Jefe +, + +900m + +, + +13.v.1977 + +G.B. Small +, genitalia vial no. M-3995 Jacqueline Y. Miller, Allyn Museum Acc. 1977-14, UF +FLMNH +MGCL 1138204 + +; + +1♀ +PT Panama, +Panama +, +Cerro Jefe +, + +900m + +, + +iii-22-1977 + +G.B. Small +, Gordon Small Collection, UF +FLMNH +MGCL 1138202 + +; + +1♁ +PT Panama, +Panama +, +Cerro Jefe +, ca. + +900m + + +iii-14-1977 + +, in cop. +G.B. Small +, Gordon Small Collection, UF +FLMNH +MGCL 1138208 + +; + +1♁ +PT +Panamá +, +Chiriquí +, +Cerro Colorado +, + +1450m + +. + +9.viii.1979 + +G.B. Small, A.C. Allyn Acc. 1972-49, UF +FLMNH +MGCL 1138198 +( +MGCL +); + + +1♁ +PT +Panamá +, +Cerro Jefe +, + +21.v.1977 + +, +G.B. Small +, genitalia vial no. M-3803 Jacqueline Y. Miller, Slide no. M-3951 append. Jacqueline Y. Miller, Allyn Museum Acc. 1977-15, UF +FLMNH +MGCL 1138205 + +; + +1♁ +PT +Panamá +, +Chiriquí +, +Cerro Colorado +, + +1450m + +. + +26.vi.1979 + +, +G.B. Small +, UF +FLMNH +MGCL 1138206 + +; + +1♁ +PT +Panamá +, +Chiriquí +, +Cerro Colorado +, + +1450m + +. + +10.viii.1979 + +, +G.B. Small +, UF +FLMNH +MGCL 1138207 + +; + +1♁ +PT +Panamá +, +Chiriquí +, +Cerro Colorado +, + +1450m + +. + +10.viii.1979 + +, +G.B. Small +, DNA voucher LEP-79424, UF +FLMNH +MGCL 1097963 +, UF +FLMNH +MGCL 1138209 +( +MGCL +) + + +; +1♁ +Coclé +, +Cerro Gaital +, + +850m +. + +, + +IV-2010 + +, +Daniel Curoe +leg (RW) + + +; +COSTA RICA +: +1♀ +Pico Volcán Orosí +, + +1440m + +, + +06/09/2002 + +, Lat. Long Decimal degrees +10.95045 +-85.54173 +, Costa Rica, coll. +P. Ríos & C. Moraga +, Voucher: D. H. Janzen & W. Hallwachs, DB: http://janzen.sas.upenn.edu + +Área de Conservación +Guanacaste + +, Costa Rica, +02-SRNP-12897 +( +MNCR +). + + + + + \ No newline at end of file diff --git a/data/38/60/33/38603375FF87E537159BFE60FC62F80D.xml b/data/38/60/33/38603375FF87E537159BFE60FC62F80D.xml new file mode 100644 index 00000000000..bc6202f674e --- /dev/null +++ b/data/38/60/33/38603375FF87E537159BFE60FC62F80D.xml @@ -0,0 +1,402 @@ + + + +A review of the genus Mirocastnia J. Y. Miller, 1980 (Lepidoptera: Castniidae) with records of recently collected specimens + + + +Author + +González, Jorge M. +0000-0001-7208-7166 +gonzalez.jorge.m@gmail.com + + + +Author + +Thöny, Hubert +Reserva Serra Bonita, P. O. Box 1, Cep 45.880 - 000 Camacan / Bahia, Brasil + + + +Author + +Worthy, Robert +10 The Hill, Church Hill, Caterham, Surrey CR 3 6 SD, U. K. + +text + + +Zootaxa + + +2024 + +2024-02-29 + + +5418 + + +3 + + +240 +254 + + + + +http://dx.doi.org/10.11646/zootaxa.5418.3.3 + +journal article +290084 +10.11646/zootaxa.5418.3.3 +9db943bf-b712-4874-9788-25c275bb2168 +1175-5326 +10726400 +E2B67801-0FEA-4D03-84C8-38884A925A3A + + + + + + + +pyrrhopygoides +( +Houlbert, 1917 +) + + + + + + + +“ + +Castnia Pyrrhopygoides + +♁, + +sp. nov. + +” +Houlbert, 1917 +: +Études de Lépidoptérologie comparée +13 +: 72. ( +Fig. 2 +). + + + + +Type material: +Described from +three male +syntypes collected by Marc Hüe de Mathan (1843–1917) in 1891. At the time of description, the specimens were in the collection of Charles Oberthür (1845–1924), they are now in NHMUK. +Miller (1980) +designated one of these syntypes as lectotype ( +Fig. 2E +), the other two become paralectotypes. + + + + + +Type locality: +Zaruma +, +Ecuador +. +Zaruma +is a town in +El Oro province +, the co-ordinates are +03°41′S +, +79°36′W +, elevation 1,200m + +. + + + + +Taxonomic status: +A valid species. Originally described in the genus + +Castnia +Fabricius, 1807 + +, as were nearly all +Castniinae +at the time, +Houlbert (1918) +then listed it in + +Athis +Hübner, [1819] + +. +Miller (1980) +transferred it to her new genus + +Mirocastnia + +, a combination subsequently followed by +Miller (1995) +and +Lamas (1995) +. + + + + +Male genitalia +: (Fig, 7D, E) The male genitalia are very similar to the other subspecies, and like them look miniaturised when compared with most +Castniidae +. Saccus is reduced. Valvae elongate along costa with a noticeable cleft along sacculus. Juxta is sclerotised. Aedeagus moderately curved, slightly recurved and sclerotised. + + + + +Distribution: +This subspecies is known from central +Colombia +to southern +Ecuador +and northern +Peru +. We know of records from +Risaralda +and +Valle del Cauca +departments in +Colombia +, and +Esmeraldas +, +Santo Domingo de los Tsáchilas +, +El Oro +, +Morona Santiago +and +Zamora Chinchipe +in +Ecuador +, and +Amazonas province +in +Peru +( +Fig. 5 +). + + + + +Discussion: +This appears to be a rare subspecies, known only from a handful of specimens. When +Miller (1980) +described the genus only the +types +were known to her, since then only a few more specimens have been found. In recent years a reasonable number of dealers’ specimens marketed as + +M. pyrrhopygoides + +have been available from +Huánuco +in +Peru +, but these are referable to + +ssp. +canis + +. + +One noticeable feature of many males of this subspecies is that there is an overscaling of dark scales on the forewing which makes the transverse semi-hyaline band seem less evident. + +The species was so named because of its resemblance to species in the +Hesperiidae +subfamily +Pyrrhopyginae +. + + + + +Material examined: +20 males +and +4 females +were examined for this study: +COLOMBIA +: +1♀ +Risaralda +, Santa Cecilia-Tapartó, +1000 m +, +XI-1982 +, J. Salazar leg. ( +JS +); 1♁, +1♀ +Cerro San Antonio, Valle [del +Cauca +], Colombia, Coll. L. Constantino ( +LC +); +ECUADOR +: ♁ LT Zaruma, Equateur, M de Mathan, 1891, No. 45, +LECTOTYPE +Castnia pyrrhopygoides +designated by Jacqueline Y. Miller. 1977, +NHMUK +010605304, vial +NHMUK +010402735; ♁ PLT +pyrrhopygoides Houlb +[ert]., Zaruma, Equateur, M de Mathan, 1891, 63.26, Joicey Bequest. Brit. Mus., +PARALECTOTYPE +Castnia pyrrhopygoides +designated by Jacqueline Y. Miller. 1977, +NHMUK +010605302; ♁ PLT Zaruma, Equateur, M de Mathan, 1891, +PARALECTOTYPE +Castnia pyrrhopygoides +designated by Jacqueline Y. Miller. 1977, +NHMUK +010605303; + +HT of + +subcoerulea + +, subcoerulea 1919 R[othschild], Ecuad[or], 339., Joicey Bequest. Brit. Mus., +NHMUK +010305386, vial +NHMUK +010402734; ♁ +Imbabura +, Lita, +X.2003 +, 600–1000, Vinciguerra coll. BMNH(E) 2023-38 +NHMUK +015547969 ( +NHMUK +); 1♁ ESM [ +Esmeraldas +], Lita, + +800m +. + +, II-08; 1♁ Macas, 09-2015, UF +FLMNH +MGCL +1138273 ( +MGCL +); +1♀ +Ecuador, Prov. +Santo Domingo de los Tsáchilas +, Otongachi, Unión del Toachi, +00°18´S +– +78°57´W +, +01.–30.VI.2017 +, leg. I. Tapia, Col. Thöny H. ( +HT +); 2♁♁ Río Chuchuví, Lita, +Esmeraldas +, + +650m +. + +, +7-IV-2004 +, leg. I Aldas; 1♁ Río Chuchuví, Lita via San Lorenzo, +Esmeraldas +, + +750m +. + +, +July2004 +( +HG +); 1♁ Chuchuví, + +800m +. + +Lita— +Esmeraldas +, +VI.2003 +; 1♁ Chuchuví, + +200m +. + +Lita— +Esmeraldas +, +VI.2003 +; 1♁ Chuchuví, +Esmeraldas +, + +800m +. + +, +VI.2003 +; 1♁ Ecuador occidente, Lita— +Esmeraldas +, +1000m +. +II.2004 +; 1♁ Lita, +1000m +. +IV.2004 +( +RW +); 4♁♁ Guaguayme Alto, Lita, +Zamora Chinchipe +, +1500m +., +September 2020 +, leg. I Aldas (Anon); +PERU +: 1♁ Falso Paquisha, PV (Puesto de Vigilancia) 22, alto Río Comaina, Cordillera del Cóndor, +Amazonas +, +800m +, +31.x.1987 +, +03º58’S +, +78º25’W +, leg. G. Lamas ( +MUSM +). + + + + \ No newline at end of file diff --git a/data/38/60/33/38603375FF88E537159BFA1FFD77FEBF.xml b/data/38/60/33/38603375FF88E537159BFA1FFD77FEBF.xml new file mode 100644 index 00000000000..ec4ebdb02d2 --- /dev/null +++ b/data/38/60/33/38603375FF88E537159BFA1FFD77FEBF.xml @@ -0,0 +1,623 @@ + + + +A review of the genus Mirocastnia J. Y. Miller, 1980 (Lepidoptera: Castniidae) with records of recently collected specimens + + + +Author + +González, Jorge M. +0000-0001-7208-7166 +gonzalez.jorge.m@gmail.com + + + +Author + +Thöny, Hubert +Reserva Serra Bonita, P. O. Box 1, Cep 45.880 - 000 Camacan / Bahia, Brasil + + + +Author + +Worthy, Robert +10 The Hill, Church Hill, Caterham, Surrey CR 3 6 SD, U. K. + +text + + +Zootaxa + + +2024 + +2024-02-29 + + +5418 + + +3 + + +240 +254 + + + + +http://dx.doi.org/10.11646/zootaxa.5418.3.3 + +journal article +290084 +10.11646/zootaxa.5418.3.3 +9db943bf-b712-4874-9788-25c275bb2168 +1175-5326 +10726400 +E2B67801-0FEA-4D03-84C8-38884A925A3A + + + + + +canis +( +Lathy, 1923 +) + + + + +“ + +Schaefferia canis +, sp. n. + +” +Lathy, 1923 +: +Annals and Magazine of natural History +(9) +12 +(68): 225–226. ( +Figs. 3 +, +4 +). + + + + + +Type material: +Described from a single female collected by Watkins ( +Figs. 3A, B +). This specimen is the holotype by monotypy, at the time of description it was in the collection of Madame Aimée de Horrack Fournier (1876–1952), it is now in NHMUK. The holotype was in all probability collected by Henry George (‘Harry’) Watkins (1886–1933) or, less probably, by his brother Casimir Watkins (1888–1955) (G. Lamas, pers. comm.). + + +Type locality: +The locality label reads: Rio Perené, Peru (Watkins). This is in the Chanchamayo region of Junín department, Peru. + + + + +Taxonomic status: +A subspecies of + +M. pyrrhopygoides +( +Houlbert, 1917 +) + + +stat. nov. + +Lathy (1923) +originally described it as a species in the genus + +Schaefferia +Houlbert, 1918 + +, following +Rothschild (1919) +. +Miller (1980) +transferred it to her new genus + +Mirocastnia + +, a combination subsequently followed by +Miller (1995) +and +Lamas (1995) +. + + + +FIGURE 4. +Size comparison of specimens of + +Mirocastnia pyrrhopygoides canis + +collected in Huánuco, Peru (RW). Scale: 10 mm. + + + +Male genitalia +: ( +Figs. 7A–C +) Despite the size of most specimens, the male genitalia look miniaturised when compared with castniids of most other genera. Saccus is reduced. Valvae elongate along costa with a prominent cleft along sacculus. Juxta is sclerotised. Aedeagus sclerotised, moderately curved, barely contorted. We did not examine the female genitalia, but it is worth noting that +Miller (1980) +separated + +M. canis + +from the other two taxa in the group by stating that “The pleural setal patch dorsad is more prominent and denser than in either + +smalli + +or + +pyrrhopygoides + +with the sclerotised pattern associated with the ostium bursae diagnostic” and also “Additional setae are found along lamella postvaginalis than in either + +pyrrhopygoides + +or + +smalli +. + +” + + + + +Distribution: +When +Miller (1980) +described the genus, only the type of + +canis + +was known to her, this was collected in Junín department, Peru but no subsequent specimens are known to have been collected in the region of the type locality. In recent years a reasonable number of dealers’ specimens have been available from Huánuco in Peru ( +Figs. 3G–J +, +4 +), but this seems to be the only area where it is collected in any numbers. Recently, some specimens have been available from San Martín department (Howard Grisham, pers. comm.), and RW obtained several specimens from Cuzco department, Peru ( +Figs. 3K–N +) and Amazonas department, Peru ( +Figs. 3C–F +); Cuzco and Amazonas seem to be major range extensions. There is one male from extreme northern Amazonas province, Peru, near the Ecuadorean border, in +MUSM +, but this is considered to represent + +ssp. +pyrrhopygoides + +due to the geographical proximity to populations of this subspecies. + + +The subspecies therefore seems to be restricted to Peru and is currently only known from Amazonas, San Martín, Huánuco, Junín, and Cuzco departments ( +Fig. 5 +). + + + + +Discussion: +When writing his original description +Lathy (1923) +only had the female +holotype +of + +subcoerulea +( +Rothschild, 1919 +) + +( +Figs. 2G, H +) with which to compare his specimen, more material is now available for comparison. The differences given by Lathy are that the abdomen of + +subcoerulea + +is entirely black whereas that of + +canis + +is white below with the anal segments orange. The abdomens on both specimens are now missing, presumably removed by Miller for genitalia dissection for her 1980 work, they have since been returned and dissection labels have been added. The likelihood is that the + +subcoerulea + +abdomen was only black due to heavy greasing, a very common occurrence in +Castniidae +. The other difference that Lathy gave is that + +subcoerulea + +lacks the marginal red patches on the dorsal hindwing. Indeed, the + +canis + +type does have faint rust-red submarginal patches between the veins on the hindwing ( +Fig. 3A +). This was considered to be the defining characteristic of the species, but recent material makes it seem unlikely to be anything more than an individual aberrant form. We have seen no specimens from Huánuco that have this feature but some females from Cuzco exhibit it, albeit much less pronounced. + + +Miller (1980) +further states that “The very prominent iridescent powder blue patch basad on hindwing below conveniently separates + +canis + +from + +pyrrhopygoides + +and + +smalli + +”. This does seem to be the defining feature of females as all specimens from Peru have this large powder-blue patch on the ventral hindwing ( +Figs. 3B, F, J, N +). Specimens of + +M. pyrrhopygoides + +and + +M. smalli + +seem to have a much-reduced patch or merely a sprinkling of blue scales ( +Figs. 1D, F +, +2D, H, L +), although this can sometimes be obscured by greasing of the very few specimens known. It also seems that the forewing transverse semi-hyaline band is narrower than in the other subspecies. + + +Even though the male of this subspecies has not been mentioned in the literature before, it is now quite wellknown. Males from Peru do show consistent small differences from + +M. p. +pyrrhopygoides + +from Ecuador and Colombia. In fact, they are more similar in appearance to + +smalli + +from Panama than they are to + +pyrrhopygoides + +sharing all the main characteristics (see + +smalli + +), except that they are usually considerably larger. + + +The recent dealers’ material from Peru has all been marketed as + +M. pyrrhopygoides + +. The female feature of the ventral basal blue patch pointed out by +Miller (1980) +, and the slight differences in the male phenotypes, show that all known Peruvian specimens, with the exception of the Amazonas specimen from the border with Ecuador, are in fact + +ssp. +canis + +. + + +A particular feature of this subspecies is the very wide size range in specimens of both sexes. In the series from Huánuco in coll. RW, forewing lengths range from 21mm to 29mm for males and 22mm to 35mm for females ( +Fig. 4 +), this could be a result of the altitude at which the specimens were collected. + + +The taxon was so named because +Lathy (1923) +thought that the pattern of the pale blue markings on the dorsal hindwing of the holotype resembles the pattern of a dog’s head, similar to the forewing of the pierid genus + +Zerene +Hübner, [1819] + +. + + + + + +Material examined: 19 males and 21 females were examined for this study: +PERU +: + +HT +Schaefferia canis Lathy + +Specimen typicum, +Río Perené +, Peru, Watkins, 60.25., Joicey Bequest. Brit. Mus., +NHMUK010605301 +, vial +NHMUK010402746 + + +; +1♁ +Huanuco +, 07/2012, +Vinciguerra +coll. +BMNH +( +E +) 2023-38 +NHMUK015548011 + +; + +1♀ +Huanuco +, 03/2011, +Vinciguerra +coll. +BMNH +( +E +) 2023-38 +NHMUK015548053 + +; + +1♀ +Tingo Maria +, 650m, +Huanuco +, +Peru +, +Las Palmas +, 27.08.04, +Vinciguerra +coll. +BMNH +( +E +) 2023-38 +NHMUK015548095 + +; + +1♀ +Carpish +, 1500–2000 masl, +Huanuco +, +September 2006 +, +Vinciguerra +coll. +BMNH +( +E +) 2023-38 +NHMUK015548137 +( +NHMUK +) + +; + +1♁ +Tingo María +, +Huánuco +, 700m., +August 2008 + +; + +1♁ +, +1♀ +idem, +August 2011 + +; + +1♁ +Carpish +Pass, +Huánuco +, 10-2010 + +; + +1♀ +Contamana +, +Río Ucayali +, +Loreto +, 10/2009 (this locality is doubtful as the altitude and habitat in this region is not suitable for the species) ( +DC +) + +; + +2♁♁ +, +3♀♀ +Nueva Cajamarca +, 125 km NW of +Tarapoto +, +San Martín +, 1100m., +March 2020 +, ( +5.95S +77.32W +) + +; + +2♁♁ +Mallqui +, 50 km S of +Tingo Maria +, +Huánuco +, 1150m., +October 2016 +, ( +9.36S +76.02W +) + +; + +1♁ +idem, +March 2018 +( +HG +) + +; + +3♁♁ +, +2♀♀ +Rodríguez de Mendoza +, +Amazonas +, 1800m., +December 2019 +, +06° 24´S +77° 26´W + +; + +1♀ +Tingo María +, +Huánuco +, 700m., +August 2007 + +; + +1♁ +, +2♀♀ +idem, +August 2008 + +; + +2♀♀ +Mallqui +, +Huánuco +, +September 2013 + +; + +1♁ +, +1♀ +Carpish +, +Huánuco +, +October 2010 + +; + +2♁♁ +idem +, +August 2011 + +; + +1♁ +, +3♀♀ +Patria +, +Valle Cosñipata +, +Cuzco +, +657m. +, +July 2019 +, +12°58´11” S +, +71°25´19”W + +; + +2♁♁ +Quincemil +, +Valle Marcapata +, +Cuzco +, +980m. +, +July 2019 +, +13°15’05”S +70°46’17”W +( +RW +) + +; + +1♀ +Peru +, +Huánuco +, Tingo María, 2300m [obviously, this elevation must refer to Carpish, not to “Tingo Maria” (G.Lamas, pers. comm.)], iii.[20]12, +M. Simon +, +MGCL +Accession No. 2012- 16, DNA Voucher LEP-79395, UF FLMNH +MGCL 1096935 +( +MGCL +) + +; + +1♀ +Huánuco +, 2000–2500m., +XI/2003 + +; + +1♀ +Carpish Pass +, +Huánuco +, 2400m., +IX/2011 +(Anon). + + + + + \ No newline at end of file diff --git a/data/38/60/4F/38604F699BB152E0B3048DE69A1F8755.xml b/data/38/60/4F/38604F699BB152E0B3048DE69A1F8755.xml new file mode 100644 index 00000000000..346d74dd27b --- /dev/null +++ b/data/38/60/4F/38604F699BB152E0B3048DE69A1F8755.xml @@ -0,0 +1,294 @@ + + + +Morphological and phylogenetic analyses reveal two new species and a new record of Phyllosticta (Botryosphaeriales, Phyllostictaceae) from Hainan, China + + + +Author + +Zhang, Zhaoxue +https://orcid.org/0000-0002-4824-9716 +College of Life Sciences, Shandong Normal University, Jinan, 250358, China & Shandong Provincial Key Laboratory for Biology of Vegetable Diseases and Insect Pests, College of Plant Protection, Shandong Agricultural University, Taian, 271018, China + + + +Author + +Liu, Xiaoyong +College of Life Sciences, Shandong Normal University, Jinan, 250358, China + + + +Author + +Zhang, Xiuguo +College of Life Sciences, Shandong Normal University, Jinan, 250358, China + + + +Author + +Meng, Zhe +College of Life Sciences, Shandong Normal University, Jinan, 250358, China +zmeng@sdnu.edu.cn + +text + + +MycoKeys + + +2022 + +2022-07-04 + + +91 + + +1 +23 + + + + +http://dx.doi.org/10.3897/mycokeys.91.84803 + +journal article +http://dx.doi.org/10.3897/mycokeys.91.84803 +1314-4049-91-1 +641F2C504C6A560DA710838E84A32F16 + + + + +Phyllosticta pterospermi Z.X. Zhang, X.Y. Liu, Z. Meng & X.G. Zhang +sp. nov. + + + + +Fig. 3 + + + + +Type +. + + + +China +, +Hainan Province +: + +Bawangling National Forest +Park + +, on diseased leaves of + +Pterospermum heterophyllum + +, +19 May 2021 +, +Z.X. Zhang +( +holotype +, HSAUP210104; ex-holotype living culture SAUCC210104) + +. + + + +Etymology. + +The specific epithet " +pterospermi +" refers to the genus name of the host plant + +Pterospermum heterophyllum + +. + + + +Description. + +Leaf endogenic and associated with leaf spots. Asexual morph: Conidiomata pycnidial, mostly aggregated in clusters, black, erumpent. On MEA, pycnidia exudes yellow conidial masses, within 15 days or longer. Pycnidial walls multilayered, textura angularis, brown, up to 30 +μm +thick; inner walls of hyaline. Conidiophores indistinct, often reduced to conidiogenous cells. Conidiogenous cells, cylindrical, hyaline, smooth, 7.5-11.0 +x +2.5-4.5 +μm +. Conidia 8.0-12.0 +x +4.5-8.5 +μm +, mean ++/- +SD = 9.8 ++/- +0.9 +x +7.3 ++/- +0.7 +μm +, hyaline, aseptate, thin and smooth-walled, coarsely guttulate or with a single large central guttule, obovoid, ellipsoidal to subglobose, enclosed in a thin mucoid sheath, 1.0-2.0 +μm +thick and bearing a hyaline, apical mucoid appendage, 4.0-6.8 +x +1.5-3.0 +μm +, flexible, unbranched, tapering towards an acutely rounded tip. + + + +Figure 3. + +Phyllosticta pterospermi + +(holotype SAUCC210104) +a +diseased leaf of + +Pterospermum heterophyllum + +b, c +colonies (left-above, right-reverse) after 15 days on PDA ( +b +) and MEA ( +c +) +d +conidiomata +e-h +conidiogenous cells with conidia +i-j +conidia. Scale bars: 10 +μm +( +e-j +). + + + + +Culture characteristics. +Colonies on PDA 80-90 mm in diameter after 14 days at 25 °C in darkness, with a growth rate of 5.7-6.5 mm/day, undulate at edge, grey white to greyish-green in obverse and reverse. Colonies on MEA 82-86 mm in diameter after 14 days at 25 °C in darkness, with a growth rate of 5.8-6.2 mm/day, undulate at edge, grey white to yellow in obverse and reverse, with moderate aerial mycelia on the surface, with black, gregarious conidiomata. + + +Additional specimen examined. + +China, Hainan Province: Bawangling National Forest Park, on diseased leaves of + +Pterospermum heterophyllum + +. 19 May 2021, Z.X. Zhang, paratype HSAUP210106, ex-paratype living culture SAUCC210106. + + + +Notes. + +Two isolates from leaf spots of + +Pterospermum heterophyllum + +phylogenetically clustered into a well-supported clade (1.00/100), which is closely related to + +P. ardisiicola + +(0.90/62) and + +P. mangiferae + +(0.99/91; Fig. +1 +). However, + +P. pterospermi + +differs from + +P. ardisiicola + +by 30 nucleotides (13/603 in ITS, 3/553 in LSU and 14/248 ACT) and from + +P. mangiferae + +by 29 nucleotides (7/567 in ITS, 2/763 in LSU, 3/215 in +tef1 +, 3/226 in ACT and 14/643 in GPDH). In morphology, they are distinguished by hosts and conidial size (8.0-12.0 +x +4.5-8.5 +μm +in + +P. pterospermi + +vs. 7.0-11.0 +x +5.0-7.5 +μm +in + +P. ardisiicola + +vs. 10.0-12.0 +x +6.0-7.0 +μm +in + +P. mangiferae + +). Furthermore, + +P. pterospermi + +differs from + +P. ardisiicola + +and + +P. mangiferae + +by wider conidiogenous cells (7.5-11.0 +x +2.5-4.5 +μm +vs. 5.0-12.5 +x +1.2-2.5 +μm +) and from + +P. mangiferae + +in having longer conidiogenous cells (7.5-11.0 +x +2.5-4.5 +μm +vs. 6.0-10.0 +x +3.0-4.0 +μm +) ( +Motohashi et al. 2008 +; +Glienke et al. 2011 +). Therefore, we establish this strain as + +P. pterospermi + +sp. nov. ( +Jeewon and Hyde 2016 +). + + + + \ No newline at end of file diff --git a/data/38/61/11/3861119E1C982E35B661CB0E0A0B397C.xml b/data/38/61/11/3861119E1C982E35B661CB0E0A0B397C.xml new file mode 100644 index 00000000000..68eca0d3a10 --- /dev/null +++ b/data/38/61/11/3861119E1C982E35B661CB0E0A0B397C.xml @@ -0,0 +1,170 @@ + + + +Flora der Schweiz und angrenzender Gebiete. Band 1. Pteridophyta bis Caryophyllaceae (2 nd edition): Registerzuband 1 + + + +Author + +Hess, Hans Ernst + + + +Author + +Landolt, Elias + + + +Author + +Hirzel, Rosmarie + +text + +1972 +Birkhaeuser Verlag + + +https://doi.org/10.5281/zenodo.291815 + +book +291815 +10.5281/zenodo.291815 +3-7643-0843-5 + + + +<subSubSection id="D82A778B73DD55B11D7CE1042F6642F6" pageId="null" pageNumber="762" type="nomenclature"> +<paragraph id="F28C2F9A1CF1CBE57B739D8B8A6C0FBE" pageId="null" pageNumber="762"> +<taxonomicName id="C96B84A5867A90FE81D814E86DB9B2FE" ID-CoL="688F5" ID-ENA="34272" authority="L." class="Magnoliopsida" family="Amaranthaceae" genus="Atriplex" kingdom="Plantae" order="Caryophyllales" pageId="null" pageNumber="762" phylum="Tracheophyta" rank="species" species="hortensis"> +<pageBreakToken id="C97BC2CC10791089F4BCCBEE6C104DC0" pageId="null" pageNumber="762" start="start">Atriplex</pageBreakToken> +<normalizedToken id="936877A7993DA3CCAE92819B5D482FAB" originalValue="horténsis" pageId="null" pageNumber="762">hortensis</normalizedToken> +L. +</taxonomicName> +</paragraph> +</subSubSection> +<subSubSection id="A111EF1A571F90AD0C91601FEEB484E6" pageId="null" pageNumber="762" type="vernacular_names"> +<paragraph id="F9A388F2A24CBF9872D08291BC54B8CE" pageId="null" pageNumber="762">Garten-Melde</paragraph> +</subSubSection> + + + +1 +jaehrig +, bis 2,5 m hoch, mit steil aufgerichteten +Seitfenaesten +. +Blaetter +meist +wechselstaendig +, im +Umriss +3eckig, +gross +, bis 10 cm lang, 1- +11/2 +mal so lang wie breit, am Grunde +herzfoermig +oder +spiessfoermig +, mit stumpfer Spitze, ganzrandig oder geschweift, +aeltere +Blaetter +beiderseits +gruen +, +juengere +graugruen +; Blattstiel bis 2 cm lang. +Gesamtbluetenstand +reichbluetig +, aus end- und +seitenstaendigen +, rispigen oder traubigen +Bluetenstaenden +bestehend. ♂ +Blueten +klein, unscheinbar. +2 verschiedene Typen von +♀ + +Blueten +: Solche mit 5 +Perigonblaettern +, wobei keine +Vorblaetter +vorhanden und die +Fruechte +senkrecht zur +Laengsrichtung +abgeflacht sind und solche mit 2 auffallend +groβen +, rundlichen oder breit ovalen, bis zum Grunde freien +Vorblaettern + +( +groesster +Durchmesser meist 10-15 mm), + +wobei keine +Perigonblaetter +vorhanden und die +Fruechte +in der +Laengsrichtung +abgeflacht sind; +Vorblaetter +nie mit +Anhaengseln +. - + +Bluete +: Sommer. + + +Zytologische Angaben. 2n += +18: +Material aus Ungarn und aus +Europa +(Baksay in +Loeve +und +Loeve +1961, +Loeve +und +Loeve +1961). + + +Standort. +Kollin, selten montan. Auf Ruderalstellen und +Schuttplaetzen +in trockenen Gegenden; gelegentlich verwilderte, heute ziemlich selten gewordene Gartenpflanze. + + + +Verbreitung. +A. hortensis + +ist wahrscheinlich durch Selektion aus der vorderasiatischen + +A. nitens + +(Nr. 2) entstanden. - Im Gebiet ziemlich verbreitet, aber selten. + + + +Bemerkungen. +A. hortensis + +ist eine alte +Gemuesepflanze +, die wahrscheinlich schon im Altertum nach Mitteleuropa kam (Verwendung wie Spinat). + + + + \ No newline at end of file diff --git a/data/38/61/7F/38617F14E4865AE581D4A40185CA76BE.xml b/data/38/61/7F/38617F14E4865AE581D4A40185CA76BE.xml new file mode 100644 index 00000000000..77294158982 --- /dev/null +++ b/data/38/61/7F/38617F14E4865AE581D4A40185CA76BE.xml @@ -0,0 +1,1776 @@ + + + +Description of a new troglobitic Sinocyclocheilus (Pisces, Cyprinidae) species from the upper Yangtze River Basin in Guizhou, South China + + + +Author + +Shao, Wei-Han +Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China + + + +Author + +Cheng, Guang-Yuan +Guiyang Bureau of Ecology and Environment, Guiyang, China + + + +Author + +Lu, Xiao-Long +Guiyang Qianren Ecological Conservation Center, Guiyang, China + + + +Author + +Zhou, Jia-Jun +0000-0003-1038-1540 +Zhejiang Forest Resource Monitoring Center, Hangzhou, China & Zhejiang Forestry Survey Planning and Design Company Limited, Hangzhou, China + + + +Author + +Zeng, Zhi-Xuan +0000-0001-9740-1342 +The Department of Endocrinology, Branch of National Clinical Research Center for Metabolic Diseases, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China + +text + + +Zoosystematics and Evolution + + +2024 + +2024-05-14 + + +100 + + +2 + + +515 +529 + + + +journal article +10.3897/zse.100.119520 +5B410772-DA79-437F-8ABB-A047B4FDC604 + + + + + +Sinocyclocheilus guiyang + +sp. nov. + + + + +Fig. 2 +, +Table 2 + + + + +Type materal. + + + + + +Holotype + +. + + +IHB +202012250001 + +, 124.0 mm +SL +; +China +: +Guizhou Province +: +Guiyang City +: +Qingzhen County +: a subterranean stream tributary of the +Wujiang System +in the +upper Yangtze River Basin +, + +26 ° 50 ' 26 " N +, +106 ° 16 ' 37 " E + +, + +1250 m + +elevation; +Jia-Jun Zhou +, + +Dec 2020 + +. + + + + + + +Paratypes + +. + + +IHB +201911140001 + +, +1 specimen +, +57.5 mm +SL +; +Zhi-Xuan Zeng +, + +Nov 2019 + +; other data same as holotype + +. + + +IHB +202012250002 + +, +1 specimen +, +86.4 mm +SL +; collected with holotype + +. + + +IHB +202207260001 + +, + +GXU +202207260002 + +– 04, +4 specimens +, +124.3–174.1 mm +SL +; +Jia-Jun Zhou +, + +Jul 2022 + +; other data same as holotype + +. + + + + +Diagnosis. + + + +Sinocyclocheilus guiyang + +is distinguishable from all other congeners by a combination of the following characters: tip of maxillary barbel not reaching to posterior edge of preoperculum, horn-like structure in forehead absent, eye absent or highly reduced, pectoral fin not significantly extending beyond base of pelvic fin. The major diagnostic characters for + +S. guiyang + +and related species are summarised in Table +3 +. + + + + +Description. + + +Morphometric measurements of +type +specimens have been transferred to percentage of standard length ( +SL +), as summarised in Table +2 +. Body laterally compressed; maximum body depth positioned at insertion of dorsal-fin. Dorsal profile convex from snout tip to dorsal-fin base end and slightly concave after dorsal-fin base. Ventral profile of pre-anal part slightly convex and slightly concave after anal-fin origin. + + + + + + +Morphometric characters of + +Sinocyclocheilus guiyang + +. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
CharacterHolotypeHolotype + Paratypes (n = 7)
RangeMeanSD
Standard length (mm)124.057.5 – 144.1--
+ +In Percentage of +SL +(%) + +
Body depth29.826.7–33.129.42.1
Predorsal length55.453.6–59.655.92.1
Dorsal-fin base length16.815.3–16.815.80.8
Dorsal-fin length18.817.6–24.520.22.2
Pre-anal length71.470.8–75.773.21.8
Anal-fin base length9.87.5–10.29.21.0
Anal-fin length16.616.0–18.317.10.9
Prepectoral length31.330.7–35.732.51.6
Pectoral-fin base length4.44.0–4.64.30.2
Pectoral-fin length21.320.8–22.221.50.5
Prepelvic length50.650.6–55.352.91.6
Pelvic-fin base length5.74.5–5.75.20.4
Pelvic-fin length16.515.4–19.817.31.4
+Caudal peduncle length ( +CPL +) +19.516.5–20.718.51.5
+Caudal peduncle depth ( +CPD +) +11.810.0–13.211.21.2
Head length31.530.2–34.132.21.4
Head depth19.016.8–21.019.141.3
Head width16.010.4–17.615.32.4
Snout length10.99.9–11.010.50.5
Eye diameter3.53.5–5.94.61.2
Interorbital width10.48.3–10.59.70.8
Prenostril length5.74.5–6.05.60.5
Width between posterior nostrils7.25.8–7.46.60.6
Upper jaw length10.210.1–10.310.20.1
Lower jaw length9.48.9–9.59.20.2
Mouth width8.36.8–8.37.50.6
Rostral barbel length5.24.9–7.16.20.9
Maxillary barbel length5.95.8–8.37.10.9
+CPD +to +CPL +ratio +0.600.55–0.670.610.04
+
+ + + + + +Major diagnostic characters for + +Sinocyclocheilus guiyang + +and its close congeners. n / a, not available. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Characters +S. guiyang + +S. multipunctatus + +S. punctatus + +S. sanxiaensis + +S. jinxiensis + +S. jiuxuensis + +S. mashanensis + +S. brevibarbatus + +S. yangzongensis +
EyeAbsent or highly reducedNormalNormalAbsentAbsentNormalNormalNormalNormal
Tip of maxillary barbelReaching to posterior edge of orbitReaching to posterior edge of preoperculumReaching to anterior edge of orbitNot reaching to anterior edge of orbitReaching to posterior edge of orbitReaching or extending to posterior edge of orbitExtending to anterior edge of orbitNot reaching to anterior edge of orbitExtending to anterior edge of orbit
Pectoral-fin extending to pelvic-fin insertionYesNoYesYesYesYesYesYesNo
Gill rakers10n / a7 – 8713–148–107–98–98 – 11
Lateral-line scales45 – 4753–6048–604138–4142–5147–5049–5171 – 81
Degenerated body scales above and below lateral lineYesYesYesYesNoYesYesYesYes
Black blotches on bodyAbsentPresentPresentAbsentAbsentAbsentAbsentAbsentPresent
+
+ +Head slightly compressed, conical in lateral view. Eyes absent (5) or highly reduced and partially covered with skin (2). Eye orbits located in dorsal anterior part of head, filled with soft tissue. Nostrils located at midway between snout tip and anterior margin of orbit; anterior nostril with rim forming an oblique tube, posteriorly thickening and elongating; posterior nostril open and elliptical. Snout blunt in dorsal view and slightly pointed in lateral view. Mouth subterminal and arched; with two pairs of barbels; rostral pair positioned anterior to anterior nostril, extending to the insertion of anterior margin of orbit, being 6.2 % (4.9 – 7.1 %) of +SL +; maxillary pair positioned at corners of mouth, extending to the posterior margin of orbit, being 7.1 % (5.8 – 8.3 %) of +SL +. Gill opening large; opercular membranes not connected at isthmus. Joints of dentary-angulars not close at isthmus. Ten outer rakers (1) on first gill arch. Pharyngeal teeth pattern 1, 3, 4 – 4, 3, 0 (1); tooth tip pointed and compressed. Vertebrae 36 (2) (Fig. +2 C +). + + + + + + + +Sinocyclocheilus guiyang +, +IHB + +202012250001, holotype, 124.0 mm +SL +; China: Guizhou Province: Guiyang City: Qingzhen County: Yangtze River Basin. +A. +Lateral view; +B. +Lateral, dorsal and ventral view of head; +C. +Micro-CT graph and reconstructed pharyngeal dentition; +D. +Live photo. Scale bar: 1 cm. + + + +Dorsal fin with 3 unbranched and 8 (5) or 9 (2) branched rays, with last one divided at base; dorsal-fin length being 20.2 % (17.6 – 24.5 %) +SL +; origin closer to snout tip than to caudal-fin base; distal margin slightly concave, last unbranched ray strong, with serration on posterior edge; last unbranched ray split to base. Pectoral fin with 1 unbranched and 14 (6) or 15 (1) branched rays; tip extending to pelvic-fin insertion; pectoral-fin length being 21.5 % (20.8 – 22.2 %) of +SL +. Pelvic fin with 1 unbranched and 7 branched rays; inserted slightly posterior to dorsal-fin origin; tip not reaching to anus. Anal fin with 3 unbranched and 5 branched rays, last one divided at base; distal margin slightly concave; origin closer to pelvic-fin insertion than to caudal-fin base. Caudal fin deeply forked, with 17 (6) or 18 (1) branched rays; upper and lower lobes pointed. + +Body covered with small scales, partially embedded subcutaneously; scales on lateral line slighter larger than other. Lateral line complete and horizontal, with 45 (4), 46 (2) or 47 (1) perforated scales. Scale rows above lateral line 20 (1), 21 (3), 22 (2) or 24 (1); below 13 (2) or 14 (5). Circumpeduncular scales 32 (1), 33 (1), 34 (2), 35 (2) or 36 (1). + +All original morphometric measurements and meristic counts are available in Suppl. material +1 +. + +
+ + +Colouration. + + +In freshly collected individuals (Figs +2 D +, +3 +), head and body generally pinkish, with or without pigments dorsally. A pair of dark stripes present on dorsal-posterior part of head, extending to dorsal mid-point of nape; a gold stripe extending along dorsal mid-line from nape to dorsal-fin origin. All fins transparent. + + + + + + +Intraspecific morphological variations of + +Sinocyclocheilus guiyang + +. +A. +Individual with no eyes; +B. +Individual with highly reduced eyes, partially covered with skin; +C. +Individual with dorsal pigment; +D. +Individual without pigment. Note that individuals of both colouration types share the presence of dark stripes on the dorsal-posterior part of the head and a gold stripe along the mid-line from the nape to the dorsal-fin origin. + + + +In preserved specimens (Fig. +2 A, B +), body and head slightly yellowish, with or without pigments dorsally. Abovementioned dark stripes and gold stripe faded. All fins transparent. + + + + +Distribution and habitat. + + +This species is presently only known from a subterranean stream flowing into the Wujiang River in the upper Yangtze River Basin in Qingzhen County, Guiyang City, +Guizhou Province +, +China +(Fig. +4 +). The species inhabits pools of subterranean stream with gravel substrate (Fig. +5 +). Video record of + +Sinocyclocheilus guiyang + +in situ is available in Suppl. material +2 +. + + + + + + +Sampling sites of + +Sinocyclocheilus guiyang + +and related species in this study. + + + + + + + +Habitat of + +Sinocyclocheilus guiyang + +. +A. +The pool of a subterranean stream where + +S. guiyang + +was collected; +B. + +S. guiyang + +in situ. + + + + + +Etymology. + + +The location of the subterranean stream where this new species was first collected: Guiyang City, the capital of +Guizhou Province +, is directly utilised as a specific epithet. The common name proposed for the new species is ‘ 贵阳金线鲃’ (Guiyang Golden-line Barbel). + + + + +Morphometric comparisons. + + +Principal component analysis for + +Sinocyclocheilus guiyang + +, + +S. punctatus + +, + +S. multipunctatus + +and + +S. sanxiaensis + +, based on 29 log-transformed characters, showed that 95.23 % of total variance was explained by the first three components, including 87.24 % by PC 1, 4.79 % by PC 2 and 3.20 % by PC 3, respectively. In the PC 1 vs. PC 3 scatter plot, + +S. guiyang + +and + +S. punctatus + +form a distinct cluster from the other two congeners on the PC 3 axis (Fig. +6 A +). The characters with major loading on PC 3 included maxillary barbel length, rostral barbel length, eye diameter, width between posterior nostrils and pectoral-fin base length (Table +4 +). Further +PCA +in + +S. guiyang + +and + +S. punctatus + +demonstrated that the first three components explained 97.26 % of total variance, in which PC 1, PC 2 and PC 3 explained 93.31 %, 2.29 % and 1.66 %, respectively. + +Sinocyclocheilus guiyang + +is separated from + +S. punctatus + +on the PC 2 axis in the PC 1 vs. PC 2 scatter plot (Fig. +6 B +). Eye diameter, maxillary barbel length, width between posterior nostrils, rostral barbel length and snout width are major loading characters on PC 2 (Table +4 +). Linear regression analysis also support + +S. multipunctatus + +as distinct from + +S. guiyang + +and + +S. punctatus + +by shorter maxillary (7.2 – 13.3 % +SL +vs. 5.8 – 8.3 % in + +S. guiyang + +, 4.9 – 9.4 % in + +S. punctatus + +) and rostral barbel lengths (6.0 – 10.7 % +SL +vs. 4.9 – 7.1 % in + +S. guiyang + +, 4.9 – 6.7 % in + +S. punctatus + +) (Fig. +6 C, D +), whereas + +S. guiyang + +further differed from + +S. punctatus + +by shorter prenostril length (4.5 – 6.0 % of +SL +vs. 5.8 – 7.6 %) and higher caudal peduncle depth to caudal peduncle length ratio (0.55 – 0.67 vs. 0.45 – 0.56) (Fig. +6 E, F +). + + + + + + +A. +Scatter plot of 1 +st +and 3 +rd +principal components for + +Sinocyclocheilus guiyang + +, + +S. punctatus + +, + +S. multipunctatus + +and + +S. sanxiaensis + +; +B. +Scatter plot of 1 +st +and 2 +nd +principal components for + +S. guiyang + +and + +S. punctatus + +; relationships between +C. +Rostral barbel length and head length, +D. +Maxillary barbel length and head length for + +S. guiyang + +, + +S. punctatus + +and + +S. multipunctatus + +; relationships between +E. +Prenostril length and head length, +F. +Caudal peduncle depth and caudal peduncle length for + +S. guiyang + +and + +S. punctatus + +. + + + + + + + +PCA +loadings of the first three principal components extracted from 29 morphometric data for + +Sinocyclocheilus guiyang + +and related species. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
- + +S. guiyang + +, + +S. punctatus + +, + +S. multipunctatus + +, + +S. sanxiaensis + +S. guiyang +, + +S. punctatus +
PC 1PC 2PC 3PC 1PC 2PC 3
Standard length0.991- 0.0620.0280.9950.026- 0.045
Body depth0.948- 0.034- 0.1650.966- 0.049- 0.204
Predorsal length0.991- 0.035- 0.0220.9960.0080.050
Dorsal-fin base length0.978- 0.0900.0300.989- 0.011- 0.027
Dorsal-fin length0.9280.0270.0190.895-0.1150.376
Pre-anal length0.986- 0.0580.0370.9950.020- 0.015
Anal-fin base length0.967- 0.107- 0.0410.9740.020- 0.104
Anal-fin length0.962- 0.032- 0.0750.9850.0730.101
Prepectoral length0.990- 0.029- 0.0710.992-0.0240.074
Pectoral-fin base length0.7120.6550.1930.9630.161- 0.080
Pectoral-fin length0.978- 0.011- 0.0430.970-0.0920.132
Prepelvic length0.991- 0.0400.0200.996- 0.005- 0.008
Pelvic-fin base length0.7320.6360.0970.954- 0.019- 0.228
Pelvic-fin length0.9760.002-0.1340.9870.0970.056
Caudal peduncle length0.954- 0.0740.0490.9580.092- 0.170
Caudal peduncle depth0.957- 0.019- 0.0650.956- 0.107- 0.230
Head length0.990- 0.035- 0.0720.9970.0080.034
Head depth0.991- 0.053- 0.0460.996-0.0140.000
Head width0.972- 0.0800.0480.970-0.1040.006
Snout length0.9660.183-0.0940.983-0.0560.029
Eye diameter0.7160.3890.4080.7580.6320.056
Interorbital width0.9820.010-0.0860.979- 0.147- 0.107
Prenostril length0.9610.052-0.0360.9540.1500.045
Width between posterior nostrils0.9560.009-0.1990.959- 0.183- 0.170
Upper jaw length0.962- 0.116- 0.1790.983-0.0400.108
Lower jaw length0.964- 0.118- 0.1560.986-0.0080.103
Mouth width0.9580.031-0.0520.9540.155- 0.003
Rostral barbel length0.731- 0.4400.4920.956-0.1610.081
Maxillary barbel length0.764- 0.3000.5240.938-0.1850.169
+
+
+ + +Molecular data analyses. + + +A total of 1134 bps were included in the aligned dataset of cyt +b +gene, with 661 conservative sites, 473 variable sites, 390 parsimony informative sites and 83 singleton sites. The mean frequency of four nucleotides in the sequences of + +Sinocyclocheilus guiyang + +is A = 29.7 %, G = 14.2 %, C = 26.2 % and +T += 29.9 %. The phylogenetic trees, reconstructed by + +ML + +and +BI +methods, are identical in topology (Fig. +7 +). The monophyletic linage of + +Sinocyclocheilus guiyang + +is robustly supported by 100 % posterior probabilities and 99 % bootstrap supports and is sister to + +S. punctatus + +. The lineage of the two species clustered with the lineage comprising sequences of + +S. multipunctatus + +, + +S. cyphotergous + +and + +S. sanxiaensis +. + +Additionally, the topology of phylogenetic reconstruction in the present study supports the monophyly of the + +S. cyphotergous + +– + +S. multipunctatus + +species group. Average genetic distances derived from cyt +b +sequences of + +Sinocyclocheilus +species + +distributed in +Guizhou Province +or the Yangtze River Basin are given in Table +5 +. The intraspecific distance of + +S. guiyang + +is 0.1 % and the mean distances between the new species and other congeners range from 2.3 % (vs. + +S. punctatus + +) to 13.8 % (vs. + +S. wumengshanensis + +). + + + + + + +Phylogenetic tree of + +Sinocyclocheilus +species + +inferred from cyt +b +using Bayesian Inference and Maximum Likelihood methods. Node values show posterior probabilities / bootstrap supports if greater than 50 %. Currently known distribution of species of the + +S. cyphotergous + +– + +S. multipunctatus + +group are shown on map. + + + + + + + +Average uncorrected pairwise genetic distance (p-distance, %) derived from cyt +b +in 15 species of + +Sinocyclocheilus + +distributed in Guizhou Province or the Yangtze River Basin. Bold numbers, intraspecific distances; regular numbers, interspecific distances; n / a, not available. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
-123456789101112131415
+1. + +S. guiyang + + +0.1 +--------------
+2. + +S. multipunctatus + +2.5 +0.4 +-------------
+3. + +S. punctatus + +2.32.6 +0.7 +------------
+4. + +S. cyphotergous + +2.81.13.1 +0.8 +-----------
+5. + +S. sanxiaensis + +3.21.02.91.6 +n / a +----------
+6. + +S. longibarbus + +10.911.011.211.211.6 +n / a +---------
+7. + +S. grahami + +11.711.611.811.912.211.5 +n / a +--------
+8. + +S. wumengshanensis + +12.311.812.112.112.311.74.2 +n / a +-------
+9. + +S. angustiporus + +11.411.111.511.311.610.47.77.1 +n / a +------
+10. + +S. macrolepis + +11.511.411.911.712.011.112.712.611.5 +n / a +-----
+11. + +S. bicornutus + +10.810.911.411.111.410.312.212.411.111.3 +n / a +----
+12. + +S. zhenfengensis + +10.910.811.210.911.310.012.012.411.311.22.9 +n / a +---
+13. + +S. angularis + +11.211.211.111.511.69.611.812.311.211.62.82.4 +n / a +--
+14. + +S. longicornus + +11.911.911.811.912.410.812.312.511.311.85.86.55.9 +n / a +-
+15. + +S. xingyiensis + +11.111.111.511.311.510.112.612.811.312.02.32.91.96.3 +n / a +
+
+
+
+
\ No newline at end of file diff --git a/data/38/61/87/386187E5FFEDFF83FF75F9D5D1504F95.xml b/data/38/61/87/386187E5FFEDFF83FF75F9D5D1504F95.xml new file mode 100644 index 00000000000..1c5059327d6 --- /dev/null +++ b/data/38/61/87/386187E5FFEDFF83FF75F9D5D1504F95.xml @@ -0,0 +1,117 @@ + + + +Revision of Australian jumping spider genus Servaea Simon 1887 (Aranaea: Salticidae) including use of DNA sequence data and predicted distributions + + + +Author + +Richardson, Barry J. + + + +Author + +Gunter, Nicole L. + +text + + +Zootaxa + + +2012 + +3350 + + +1 +33 + + + +journal article +10.5281/zenodo.212467 +a23093e0-d8a3-423a-8222-73ebe53836a8 +1175-5326 +212467 + + + + + + + +Servaea +Simon, 1887 + + + + + + + +Type +species: +Scaea + +vestita +L. Koch, 1879 + +by monotypy. + + + + + +Scaea +Koch, L. + +, +1879 + +: +1142 + +[junior homonym of +<emphasis id="82BCEAE1FFEDFF83FD69F86AD0D54C18" box="[651,711,354,375]" italics="true" pageId="11" pageNumber="12">Scaea</emphasis> +Phillipi, 1844 (Mollusca)]. +<emphasis id="82BCEAE1FFEDFF83FF75F889D2FB4CF9" box="[151,233,385,406]" italics="true" pageId="11" pageNumber="12">Servaea</emphasis> +<bibRefCitation id="D4594B02FFEDFF83FF0DF888D3614CFA" author="Simon" box="[239,371,384,406]" pageId="11" pageNumber="12" refString="Simon, E. (1887) [Observations sur divers Arachnides: synonymies et descriptions]. Annales de la Societe Entomologique de France, (6) 7 (Bull.), 158, 167, 175, 186, 193." type="journal article" year="1887">Simon, 1887</bibRefCitation> +: 186 [ +<emphasis id="82BCEAE1FFEDFF83FE50F889D0064CF9" box="[434,532,385,406]" italics="true" pageId="11" pageNumber="12">nom. nov.</emphasis> +for +<bibRefCitation id="D4594B02FFEDFF83FDDFF889D0804CF9" author="Scaea" box="[573,658,385,406]" pageId="11" pageNumber="12" refString="Scaea Koch, L., 1879: 1142 [junior homonym of Scaea Phillipi, 1844 (Mollusca)]. Servaea Simon, 1887: 186 [nom. nov. for Scaea L. Koch, 1879]" type="journal article" year="1879"> +<emphasis id="82BCEAE1FFEDFF83FDDFF889D0684CF9" box="[573,634,385,406]" italics="true" pageId="11" pageNumber="12">Scaea</emphasis> +L +</bibRefCitation> + +. +Koch +, +1879 +] + + + + + +Diagnosis. +Fissident, ocular quadrangle (equal or) narrower behind, frontal surface of chelicera round, male chelicera geniculate and bowed prolaterally with transverse ridges, epigynum clearly defined with paired fossae and clear median guide, female insemination duct hardly if at all evident, level with fossae, spermatheca large, rounded and within the margin of the fossa close to the posterior edge, embolus coiled in anticlockwise direction with single coil and pointed, tegular groove covers proximal part of embolus, tegulum clearly longer than wide, with posterior lobe. Fringing on male T1. The genus can be differentiated from + +Cytaea + +as the embolus is single-coiled rather than double coiled in the male and the insemination ducts are within rather than posterior to the fossae. + +Servaea + +can be differentiated from + +Euryattus + +as the tegulum has a posterior lobe and the insemination ducts are anterior to the spermatheca and pass towards the lateral edges of the fossae. + + + + \ No newline at end of file diff --git a/data/38/61/87/386187E5FFEDFF99FF75FA46D33A4A6B.xml b/data/38/61/87/386187E5FFEDFF99FF75FA46D33A4A6B.xml new file mode 100644 index 00000000000..0a81a2f1357 --- /dev/null +++ b/data/38/61/87/386187E5FFEDFF99FF75FA46D33A4A6B.xml @@ -0,0 +1,2330 @@ + + + +Revision of Australian jumping spider genus Servaea Simon 1887 (Aranaea: Salticidae) including use of DNA sequence data and predicted distributions + + + +Author + +Richardson, Barry J. + + + +Author + +Gunter, Nicole L. + +text + + +Zootaxa + + +2012 + +3350 + + +1 +33 + + + +journal article +10.5281/zenodo.212467 +a23093e0-d8a3-423a-8222-73ebe53836a8 +1175-5326 +212467 + + + + + + + +Servaea incana +( +Karsch, 1878 +) + + + + + +Figs 6–22 + + + + + + +Plexippus incanus + +Karsch 1878 +: 25 + + +. + + + + +Scaea +vestita + +Koch L. 1879: 1142 pl. 94, +Fig. 4 +, +5 +., Peckham & Peckham 1901: 302 pl. 25, f.2. + + + +Servaea vestita +: Simon 1888: 283 + +, Proszynski 1984: 131; 1987: 105; Davies & +Zabka 1989: 220 +; + +Zabka 1991 + +52, +Platnick 2012 +unpaginated. + + + + +Plexippus validus + +Urquhart 1893 +: 127 + + +, + +Hickman 1967 +: 84 + +, f. 147–9, preoccupied; + +Plexippus validus +Thorell 1877 + +. + + + + + +Servaea incana +: + +Zabka 1991 +: 52 + + +, +Platnick 2012 +unpaginated. + + + + + +Remarks. +The +holotype +of + +S. incana + +is large but in extremely poor condition. The morphology of the female genitalia is, however, clear. The +syntype +series of + +S. vestita + +consists of three female specimens from Sydney (ZMHB MG3491), all specimens of + +S. incana +, + +and a further specimen from Peak Downs (ZMH, MG 16537, BJR1183) of a second species, + +S. narraweena + +. Accordingly, we designate a female specimen from Sydney (ZMHB MG3491A) as the +lectotype +of + +Servaea vestita +(L. Koch, 1879) + +and the remaining two Sydney specimens as +paralectotypes +, so as to stabilise usage of the names. The +type +of + +P. validus +Urquhart 1893 + +could not be found and the description is insufficient to diagnose the species, however all known specimens of + +Servaea + +from Tasmania are of + +S. incana + +(as + +S. vestita + +) and so it is considered a junior synonym of + +S. incana + +. + + + + + +Type +material. +Holotype +: + + +Plexippus incanus + +, 1F, New South +Wales +, ( +ZMHB +MG1735 +BJR +960); + + + +Lectotype +: + + +Scaea +vestita + +, 1F, New South +Wales +, Daemel, ( +ZMHB +MG 3491A +BJR +1209). + + + +Paralectotypes +: + + +Scaea +vestita + +2F New South +Wales +, Daemel, ( +ZMHB +MG3491 +BJR +1209). + + +Other material examined. QUEENSLAND: +2F, Mt Beauty, Eucalyptus, +144.31°E +, +17.38°S +, +23 Dec +, 1990, (QM S 73118, +BJR +898); 1F, Benaraby Rest Area, +151.31°E +, +24.00°S +, +20 Jul +, 1992, A.F. Longbottom, ( +WAM +T66953, +BJR +497); 1F, Emu Park, +150.78°E +, +23.25°S +, +20 Nov +, 1990, M. +Zabka +, (QM S 73116, +BJR +910); 1F, Kroombit Tops, Lower Kroombit Creek, +45km +SSW Calliope, open forest, under log, +151.033°E +, +24.35°S +, +9 Dec +, 1983, V. Davies, J. Gallon, (QM +S 73088 +, +BJR +905); 2F, Maroochye River, +112 km +N of Brisbane, +152.97°E +, +26.57°S +, +1 Jul +, 1939, J.C. Wiburd, (AM +KS +37286, +BJR +792); 1F, Nanango, 152°E, +26.67°S +, +8 Nov +, 1990, (QM S 73133, +BJR +949); 3F, Caloola, 151°E, +26.73°S +, +10 Sep +, 1983, R.R. Jackson, (QM +S 55902 +, +BJR +906); 2F, +11.5km +W Wengenville, +151.58°E +, +26.83°S +, +8 Nov +, 1990, (QM +S 73112 +, +BJR +903); 1F, Bunya Mt, +151.57°E +, +26.85°S +, +9 Sep +, 1983, R.R. Jackson, (QM +S 73084 +, +BJR +953); 1M, 6F, Lake Broadwater, under bark, +151.10°E +, +27.35°S +, +16 Oct +, 1984, M. Bennie, (QM S 73101, +BJR +935); 2F, 7 imm., Lake Broadwater, +151.10°E +, +27.35°S +, +28 Jul +, 1982, M. Bennie, (QM +S 61147 +, +BJR +917); 2F, Lake Broadwater, Eucalyptus, under bark, +151.10°E +, +27.35°S +, +26 Jan +, 1985, J. Wylie, (QM S 73102, +BJR +934); 3F, Lake Broadwater, Eucalyptus, +151.10°E +, +27.35°S +, +26 Jan +, 1985, J. Thompson, (QM +S 73086 +, +BJR +938); 7F, 1 imm., Lake Broadwater, under bark, +151.10°E +, +27.35°S +, +17 Oct +, 1984, M. Bennie, (QM +S 73099 +, +BJR +942); 2M, 3F, 3 imm., Lake Broadwater, under bark, +151.10°E +, +27.35°S +, +17 Oct +, 1984, M. Bennie, (QM +S 73098 +, +BJR +907); 7F, 2 imm., Lake Broadwater, under bark, +151.10°E +, +27.35°S +, +26 Jan +, 1985, M. Bennie, V. Davies, (QM +S 73104 +, +BJR +897); 5F, Lake Broadwater, +151.10°E +, +27.35°S +, +18 May +, 1985, L. & F. Wood, (QM +S 73105 +, +BJR +901); 2F, Lake Broadwater, +151.10°E +, +27.35°S +, +17 Oct +, 1984, M. Bennie, (QM +S 73098 +, +BJR +907.2); 1M, 7F, Lake Broadwater, +151.10°E +, +27.35°S +, +21 Dec +, 1984, M. Bennie, (QM +S 73097 +, +BJR +908); 2M, 2F, Lake Broadwater, +151.10°E +, +27.35°S +, +26 Jan +, 1985, M. Bennie, V. Davies, (QM +S 73100 +, +BJR +912); 1M, 1F, Lake Broadwater, +151.10°E +, +27.35°S +, +13 May +, 1984, V. Wood, (QM +K 73103 +, +BJR +914); 1M, 1F, Girraween, +150.45°E +, +27.37°S +, +8 Sep +, 1983, R.R. Jackson, (QM +S 73087 +, +BJR +924); 1F, 1, imm., Camp Mountain, +152.87°E +, +27.40°S +, +21 Jul +, 1992, J.M. Waldock, ( +WAM +T66954, +BJR +492); 1M, Belmont, +153.02°E +, +27.47°S +, +30 Aug +, 1966, R.E. Mascord, (AM +KS +18975, +BJR +689); 1F, Brisbane, +153.02°E +, +27.47°S +, +1 Aug +, 1987, M. +Zabka +, (AM +KS +64897, +BJR +568); 1F, +6km +E Spicers Gap, +152.48°E +, +28.08°S +, +22 Nov +, 1990, (QM S 73126, +BJR +915). + +NEW + +SOUTH +WALES + +: + +1F, Girraween National Park, Eucalyptus, +151.93°E +, +28.87°S +, +26 Nov +, 1990, (QM S 73128, +BJR +954); 1M, 1F, Girraween National Park, +151.93°E +, +28.87°S +, +26 Nov +, 1990, (QM +S 73122 +, +BJR +951); 1F, +10km +S Tenterfield, Eucalyptus, +152.02°E +, +29.13°S +, +28 Nov +, 1990, (QM S 73120, +BJR +913.3); 1M, 3F, +10km +S Tenterfield, +152.02°E +, +29.13°S +, +28 Nov +, 1990, (QM S 73120, +BJR +913); 1F, 1 imm., +27km +S Glen Innes, +151.73°E +, +29.73°S +, +28 Nov +, 1990, (QM S 73114, +BJR +952); 1F, W of Bakers Ck, Bundarra Baralba Rd., under bark, +151.02°E +, +30.20°S +, +12 Sep +, 2001, H. Smith, hand, (AM +KS +75576, +BJR +772); 1F, +5km +E Armidale, +151.72°E +, +30.52°S +, +29 Nov +, 1990, (QM S 73132, +BJR +933); 1M, 1F, Walcha, +151.58°E +, +30.98°S +, +2 Oct +, 1971,M.R. Gray, (AM +KS +19219, +BJR +679); 1M, Namoi River, +57km +W Tamworth, +150.33°E +, +31.08°S +, +2 Dec +, 1990,B. Carrol, (QM S 73135, +BJR +922); 1M, 1F, Rocky Glen, +34km +E Coonabarabran, Eucalyptus, +149.57°E +, +31.12°S +, +2 Dec +, 1990, (QM +S 73134 +, +BJR +931); 2F, +5km +SE Weetaliba, NW Coolah, Eucalyptus, +149.62°E +, +31.68°S +, +4 Dec +, 1990, (QM S 73129, +BJR +950); 1M, Coolah Tops NP, Grass Tree Track., under bark, +150.00°E +, +31.73°S +, +11 Aug +, 2001, G. Milledge, hand, (AM +KS +75106, +BJR +779); 1M, Sawpit Ck, +149.83°E +, +32.08°S +, +20 Dec +, 1993, J. Noble, (AM +KS +56499, +BJR +740); 1F, +27km +N Gresford, Eucalyptus, +151.53°E +, +32.18°S +, +5 Dec +, 1990, (QM S 73117, +BJR +932); 1F, Dubbo, +148.62°E +, +32.25°S +, +31 Jul +, 1966, R.E. Mascord, (AM +KS +18348, +BJR +687); 1F, +40km +W Muswellbrook, +150.47°E +, +32.27°S +, +4 Dec +, 1990, (QM S 73113, +BJR +955); 1F, nr Deadmans Ck, +15km +NE of Gulgong, +149.65°E +, +32.28°S +, +1 Jan +, 2000, G. Milledge & H. Smith, (AM +KS +62180, +BJR +817); 1M, Mudgee, +149.58°E +, +32.60°S +, +1 Dec +, 1994, Trudgett, (AM +KS +42638, +BJR +770); 1M, Bimbadeen Lookout, SW Cessnock, under bark, +150.33°E +, +32.83°S +, +21 Apr +, 1990, D. Hirst, ( +SAM +NN +22377, +BJR +550); 1F, Yengo NP nr Finchly Trig, +150.85°E +, +32.98°S +, +1 Nov +, 1997, A. White, (AM +KS +51377, +BJR +699); 1 imm., Mullion State Forest, N of Orange, under bark, +149.13°E +, +33.18°S +, +16 Oct +, 1999, M. Gray & G. Milledge, hand, (AM +KS +59181, +BJR +728); 1M, Mullion State Forest, N of Orange, under bark, +149.13°E +, +33.18°S +, +16 Oct +, 1999, M. Gray & G. Milledge, hand, (AM +KS +59178, +BJR +720); 1F, Mullion State Forest, N of Orange, +149.13°E +, +33.18°S +, +16 Oct +, 1999, M. Gray & G. Milledge, (AM +KS +59177, +BJR +747); 1M, 4F, The Battery Picnic Area, SE of Merriwa., under bark, +150.45°E +, +33.20°S +, +11 Jun +, 2001, M. Gray, G. Milledge & H. Smith, hand, (AM +KS +75051, +BJR +782); 2M, 1F, Tarana, +149.92°E +, +33.53°S +, +24 Apr +, 1968, R.E. Mascord, (AM +KS +18277, +BJR +682); 1M, 1F, Tarana, +149.92°E +, +33.53°S +, +23 Apr +, 1966, R.E. Mascord, (AM +KS +18943, +BJR +681); 1F, Frazer Res Wahroonga, +151.13°E +, +33.72°S +, +11 Oct +, 1996, J. Noble, (AM +KS +56505, +BJR +750); 1F, Frazer Res Wahroonga, +151.13°E +, +33.72°S +, +11 Oct +, 1996, J. Noble, (AM +KS +56503, +BJR +791); 1F, Frazer Res Wahroonga, +151.13°E +, +33.72°S +, +25 Sep +, 1996, J Noble, (AM +KS +56504, +BJR +745); 1F, Waitara, +151.10°E +, +33.72°S +, +20 Sep +, 1996, J. Noble, (AM +KS +50231, +BJR +780); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +24 Oct +, 1996, J. Noble, (AM +KS +58508, +BJR +734); 1F, Conimbla NP, Wallaby Picnic Area, +148.43°E +, +33.78°S +, +14 Mar +, 2002, G. Milledge & H. Smith, (AM +KS +76349, +BJR +794); 1F, Lane Cove, +151.17°E +, +33.82°S +, +10 May +, 1966, R.E. Mascord, (AM +KS +31690, +BJR +754); 1F, Beecroft, +151.07°E +, +33.75°S +, +12 May +, 1993, J. Noble, (AM +KS +54052, +BJR +696); 1F, Beecroft, +151.07°E +, +33.75°S +, +12 Jul +, 1993, J. Noble, (AM +KS +54053, +BJR +704); 1M, 1F, Enfield, +151.10°E +, +33.88°S +, +1 Sep +, 1903, E.P. Ramsay, (AM +KS +22259, +BJR +692); 1F, Boyd Plateau Luther's Swamp, +150.13°E +, +33.98°S +, +6 Sep +, 1972, M.R. Gray, (AM +KS +17862, +BJR +688); 1F, Camden, +150.70°E +, +34.05°S +, +1 May +, 1968, M. Gray, (AM +KS +749, +BJR +570); 1F, Waterfall, +151.00°E +, +34.13°S +, +8 Dec +, 1967, (AM +KS +18284, +BJR +685); 1F, Helensburg, +151.00°E +, +34.18°S +, +25 Sep +, 1966, R.E. Mascord, (AM +KS +18988, +BJR +683); 1F, Mittagong, +150.45°E +, +34.45°S +, +1 Aug +, 1959, P. Rainbird, (AM +KS +48874, +BJR +746); 1F, Jamberoo, +150.78°E +, +34.65°S +, +30 Dec +, 1992, J. Noble, (AM +KS +58546, +BJR +751); 1F, +17km +NE Narrandera, +146.68°E +, +34.65°S +, +13 Apr +, 1983, J.T. Doyen, ( +ANIC +42 0 0 0 308, +BJR +438); 1M, 1F, Gerringong, +150.83°E +, +34.73°S +, +13 Mar +, 1997, G. Wishart, (AM +KS +50105, +BJR +753); 1F, Harley Hill +6km +E of Berry, +150.77°E +, +34.77°S +, +25 Nov +, 1997, G. Wishart, (AM +KS +51328, +BJR +703); 1M, 1F, 2 imm., Harley Hill, nr Gerringong, +150.77°E +, +34.77°S +, +21 Aug +, 1999,G Wishart, (AM +KS +65915, +BJR +799); 1F, Berry, +150.70°E +, +34.78°S +, +28 Aug +, 1966, R.E. Mascord, (AM +KS +18945, +BJR +674); 1M, 2F, Pickwick Farm, S of Gunning, +149.27°E +, +34.78°S +, +1 Dec +, 1999, M. +Zabka +& M. Gray, (AM +KS +65912, +BJR +787); 4M, 6F, Pickwick Farm, S of Gunning, woodland, under bark, +149.27°E +, +34.78°S +, +12 Dec +, 1999,M +Zabka +, (AM +KS +65910, +BJR +776); 1F, 1 imm., Murrumbateman, +149.03°E +, +34.97°S +, +6 Mar +, 1977, R. Moran, ( +ANIC +42 0 0 0 288, +BJR +425); 1M, 3F, Jervis Bay, +150.73°E +, +35.05°S +, +28 Oct +, 2002, M. +Zabka +& G. Wishart, (AM +KS +81350, +BJR +673); 2F, 1 imm., +10km +S of Wagga Wagga, nr Collorboralli Creek, under bark, +147.33°E +, +35.25°S +, +18 Apr +, 1993, C.A. Car, ( +WAM +T66949, +BJR +499); 2F, E bank Murray River nr Swan Hill, under bark, +143.57°E +, +35.33°S +, +30 Nov +, 2002, M.S. Harvey, M.E. Bosfelds, ( +WAM +T66948, +BJR +494); 1F, Albury, +146.90°E +, +36.05°S +, +28 Sep +, 1958, R.V. Southcott, ( +SAM +NN +22391, +BJR +557); 1M, Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Aug +, 1998, J Noble, (AM +KS +51659, +BJR +708); 1M, Frying Pan, Cooma, +149.13°E +, +36.23°S +, +11 Jan +, 1995, J Noble, (AM +KS +56542, +BJR +727); 1M, Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Aug +, 1994, J Noble, (AM +KS +56544, +BJR +735); 1F, Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Aug +, 1994, J. Noble, (AM +KS +56541, +BJR +716); 1M, Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Jul +, 1993, J. Noble, (AM +KS +56549, +BJR +729); 1M, Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Aug +, 1994, J. Noble, (AM +KS +56548, +BJR +736); 1F Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Aug +, 1994, J. Noble, (AM +KS +56545, +BJR +749); 1F, Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Mar +, 1992, J. Noble, (AM +KS +58569, +BJR +755); 1F, Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Mar +, 1992, J. Noble, (AM +KS +58568, +BJR +757); 1F, Frying Pan, Cooma, +149.13°E +, +36.23°S +, +18 Dec +, 1991, J. Noble, (AM +KS +56443, +BJR +758); 1F, Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Mar +, 1992, J. Noble, (AM +KS +58567, +BJR +759); 1F Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Aug +, 1994, J. Noble, (AM +KS +56543, +BJR +762); 1F, Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Mar +, 1992, J. Noble, (AM +KS +58565, +BJR +763); 1F, Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Jul +, 1993, J. Noble, (AM +KS +56495, +BJR +765); 1F, Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Mar +, 1992, J. Noble, (AM +KS +56452, +BJR +767); 1F, Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Mar +, 1992, J. Noble, (AM +KS +56451, +BJR +768); 1F Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Mar +, 1992, J. Noble, (AM +KS +58566, +BJR +769); 1F, Beecroft, +151.07°E +, +33.75°S +, +11 Jan +, 1995, J. Noble, (AM +KS +56546, +BJR +778); 1F, Frying Pan, Cooma, +149.13°E +, +36.23°S +, +12 Mar +, 1993, J. Noble, (AM +KS +56547, +BJR +785); 1F, Eurobodalla N.P., Mystery Bay. under bark, +150.12°E +, +36.30°S +, +26 Dec +, 2004, G. Milledge, (AM +KS +90904, +BJR +702); 1F, Bombala, +149.25°E +, +36.92°S +, 1929, Rev A.J. Barrett, (AM +KS +19218, +BJR +684). +AUSTRALIAN CAPITAL TERRITORY: +1 imm., Mulligans Flat Nature Reserve, +ACT +, Eucalyptus, under bark, +149.15°E +, +35.20°S +, +16 Feb +, 2011, B.J. Richardson, bark stripping, ( +ANIC +42 0 0 1500, +BJR +1190); 2F, Black Mountain, +149.10°E +, +35.27°S +, +20 Aug +, 1986, W. Rafferty, ( +ANIC +42 0 0 0 293, +BJR +430); Canberra, +149.13°E +, +35.30°S +, 1960, E. McCallan, ( +ANIC +42 0 0 0 291, +BJR +428); 1F, Northbourne Plantation, +149.13°E +, +35.30°S +, +15 Sep +, 1933, W.J. Rafferty, ( +ANIC +42 0 0 0 285, +BJR +422); 1F, +5km +NE Piccadilly Circus, +ACT +, +148.80°E +, +35.37°S +, +1 Mar +, 1982, D.C.F. Rentz, ( +ANIC +42 0 0 1125, +BJR +870); 1F, +10km +W Cotter River, +ACT +, +148.73°E +, +35.40°S +, +10 Dec +, 1987, M. Baehr, (QM S 73123, +BJR +945); 1M, Murrumbidgee River +3km +Cotter River, +149.05°E +, +35.43°S +, +20 Dec +, 1984, (QM S 73130, +BJR +927); 1F, +5km +S Cotter River, +148.85°E +, +35.45°S +, +11 Dec +, 1983, M. Baehr, (QM S 73125, +BJR +944); 2M, Canberra, +148.83°E +, +35.57°S +, 1929, G.F. Hill, ( +ANIC +42 0 0 0 318, +BJR +501). +VICTORIA: +1M, 1F, Campaspe River, N of Rochester, under bark, +144.68°E +, +36.27°S +, +23 May +, 1988, D. Hirst, ( +SAM +NN +22385 6, +BJR +551); 2F, +40km +E Tallangatta, Vict, Eucalyptus, +147.82°E +, +36.28°S +, +13 Nov +, 1990, (QM +S 73108 +, +BJR +941); 1F, 1 imm., Wangaratta, +146.32°E +, +36.35°S +, +29 May +, 1963,E.F. Riek, ( +ANIC +42 0 0 0 286, +BJR +423); 1F, +30km +W Cooma, Eucalyptus, +144.72°E +, +36.42°S +, +11 Dec +, 1990, (QM S 73131, +BJR +909); 1F, Dimboola, +142.72°E +, +36.45°S +, +25 May +, 1988, D. Hirst, ( +SAM +NN +22378, +BJR +535); 1F, +5km +W Gabsted, NW Myrtleford, Eucalyptus, +146.73°E +, +36.57°S +, +5 Dec +, 1990, (QM S 73127, +BJR +920); 1M, +12km +NNE Mansfield, +146.13°E +, +36.95°S +, +15 Dec +, 1990, (QM S 73124, +BJR +946); 1F, Spring Vale, +144.90°E +, +37.00°S +, +11 May +, 1965, R.V. Southcott, ( +SAM +NN +22389, +BJR +536); 1M, 1F, Deep Lead, +1km +SW, under bark, +142.72°E +, +37.00°S +, +21 Jun +, 1989, D. Hirst, ( +SAM +NN +22387 8, +BJR +541); 1F, +5km +SW Eilden, +145.92°E +, +37.23°S +, +16 Dec +, 1990, (QM +S 73109 +, +BJR +948); 1F, Anakie Junction, +1km +NW, Brisbane Ranges, under bark, +144.25°E +, +37.88°S +, +2 Jun +, 1989, D. Hirst, ( +SAM +NN +22390, +BJR +539); 1M, 1F, Churchill, peridomestic, +146.45°E +, +38.30°S +, +28 Dec +, 1992, R. de Sousa Daw, ( +SAM +NN +22381 2, +BJR +553); 1F, Churchill, peridomestic, +146.45°E +, +38.30°S +, +16 Nov +, 1993, R. de Sousa Daw, ( +SAM +NN +22380, +BJR +516);: 2F, 2imm., Churchill, +146.45°E +, +38.30°S +, +7 Aug +, 1999, R. de Sousa-Daw, ( +SAM +NN +22383-4, +BJR +552); 1M, 2F, Spring Creek, Torquay, +144.32°E +, +38.33°S +, +26 Dec +, 1982, ( +ANIC +42 0 0 0 289, +BJR +426); 1M, Billys Creek Section, Morwell Natl Park, +146.42°E +, +38.35°S +, +12 Apr +, 2003, K. Harris, ( +SAM +NN +22379, +BJR +517); 1F, +17km +E of Naringal, Eucalypts, under bark, +142.80°E +, +38.42°S +, +27 Aug +, 1978,Parnaby, (AM +KS +44483, +BJR +798); 1F, 6 imm., Separation Creek, +143.90°E +, +38.63°S +, +19 Sep +, 1989, M.S. Harvey, M.E. Blosfelds, ( +WAM +T66952, +BJR +498). +TASMANIA: +1M, Forth Falls, +146.22°E +, +41.38°S +, +28 Dec +, 1926, Hickman, (AM +KS +31084, +BJR +800); 1M, Punch Bowl, +147.17°E +, +41.45°S +, +24 Aug +, 1928, V.V.Hickman, (AM +KS +31063, +BJR +801); 1F, West Darlington, Maria Is. +148.07°E +, +42.58°S +, +14 Apr +, 1968, A.J. Dartnall, (TM J814, +BJR +1121); 1F, West Moonah, +147.28°E +, +42.85°S +, +27 Oct +, 1988, Grade 6, Springfield Gardens P.S., (TM J2765, +BJR +1126); 1M, Carlton, S.E., +147.68°E +, +42.87°S +, +20 Jul +, 1963, E. Aves, (TM J824, +BJR +1118); 2F, Hobart, +147.32°E +, +42.88°S +, +30 Dec +, 1899, (TM J871, +BJR +1119); 1M, Hobart, +147.32°E +, +42.88°S +, +24 Jan +, 1938, D.C. Pearse, (TM J832, +BJR +1120); 1F, Hill behind New Town, +147.23°E +, +42.88°S +, Nov, 1938 G. Brownell, (TM J845, +BJR +1124); 1F, Domain, Hobart, +147.32°E +, +42.88°S +, +15 Oct +, 1962, J..F. Greenhill, (TM J870, +BJR +1125); 1F, Roches Beach, +147.50°E +, +42.90°S +, Jul, 1977, E. Turner, (TM J1280, +BJR +1117); 1F, Sloping Main, S.E., +147.68°E +, +42.98°S +, +29 Apr +, 1965, E. Aves, (TM J507, +BJR +1123). + +SOUTH +AUSTRALIA +: + +2M, 2F, Lock 4, Murray River, under bark, +140.57°E +, +34.33°S +, +18 May +, 1964,G.F. Gross, ( +SAM +NN +22363 6, +BJR +554); 3F, +3.8km +NW Keyneton, under bark, +139.10°E +, +34.53°S +, +27 Dec +, 2002, M.S. Harvey, M.E. Bosfelds, ( +WAM +T66942, +BJR +482); 2M, Para Hills, +138.65°E +, +34.80°S +, +11 Sep +, 1975, G. Crook, ( +SAM +NN +22331- 7A, +BJR +514.1); 1F, Tea Tree Gully, +138.72°E +, +34.82°S +, +30 Dec +, 1899, C. Bain, ( +SAM +NN +22339, +BJR +504); 1F, 1 imm., Millbrook Reservoir, +138.82°E +, 34.82, +7 Mar +, 2002°S, D. Hirst, J. Cox, ( +SAM +NN +22376, +BJR +522); 1M, Tea Tree Gully, +138.72°E +, +34.82°S +, +1 Jun +, 1958, J. Walsh, ( +SAM +NN +22338, +BJR +545); 1F, Chain of Ponds, now Kangaroo Creek, under bark, +138.83°E +, +34.82°S +, +30 Jun +, 1985, JJJ Szent Ivany, ( +SAM +NN +22347, +BJR +523); 1M, Blair Athol, Adelaide, +138.58°E +, +34.85°S +, May, 1987, J.A. Kairl, ( +SAM +NN +22330, +BJR +511); 1F, Norwood, +138.63°E +, +34.92°S +, +14 Mar +, 1967, R. Briggs, ( +SAM +NN +22328, +BJR +510); 1F, Norwood, +138.63°E +, +34.92°S +, +18 Aug +, 1967, R. Briggs, ( +SAM +NN +22329, +BJR +513); 2F, Norton Summit, +138.72°E +, +34.92°S +, Apr, 1967, R. Briggs, ( +SAM +NN +22345-6, +BJR +540); 14F, Adelaide Parklands, nr Dulwich, +138.62°E +, +34.93°S +, +7 Oct +, 1975, G. Cook, P. Christie, ( +SAM +NN +22306-19, +BJR +505); 1F, 1 imm., Hazelwood Park, Adelaide, +138.65°E +, +34.93°S +, Jul, 1990, H. Mincham, ( +SAM +NN +2815, +BJR +538); 1M, Adelaide Parklands, nr Dulwich, +138.62°E +, +34.93°S +, +19 Oct +, 1975, G. Crook, ( +SAM +NN +22304, +BJR +548); 1M, Adelaide Parklands, nr Dulwich, on flowering plants, +138.62°E +, +34.93°S +, +14 Sep +, 1975, G. Crook, ( +SAM +NN +22305, +BJR +520); 1F, 1 imm., Waite Institute, Netherby, +138.62°E +, +34.97°S +, +23 Sep +, 1975, R. Cook, ( +SAM +NN +22323, +BJR +503); 2F, Waite Institute, Netherby, +138.62°E +, +34.97°S +, +24 Sep +, 1975, R. Cook, ( +SAM +NN +22321-2, +BJR +509); 1F, Waite Institute, Netherby, +138.62°E +, +34.97°S +, +10 Mar +, 1977, R. Cook, ( +SAM +NN +22327, +BJR +524); 2M, 1F, Waite Institute, Netherby, +138.62°E +, +34.97°S +, +5 Dec +, 1975, R. Cook, ( +SAM +NN +22324-5, +BJR +525); 1F, Waite Institute, Netherby, +138.62°E +, +34.97°S +, +8 Dec +, 1975, R. Cook, ( +SAM +NN +22326, +BJR +530); 1F, Waite Institute, Netherby, +138.62°E +, +34.97°S +, +9 Feb +, 1936, H. Womersley, ( +SAM +NN +22320, +BJR +531); 1M, 2 imm., Blackwood, +138.62°E +, +35.02°S +, +15 May +, 1935,H. Womersley, ( +SAM +NN +22353, +BJR +526); 1M, Mylor, +138.77°E +, +35.05°S +, +11 Feb +, 1979, (QM +S 73085 +, +BJR +900); 1M, Mylor, +138.77°E +, +35.05°S +, +11 Feb +, 1979, A. Austin, (QM +S 73092 +, +BJR +929); Mylor +5km +S of, +138.77°E +, +35.05°S +, +14 Dec +, 1980, A.D. Austin, (AM +KS +10546, +BJR +686); 1F, Belair National Park, +138.65°E +, +35.03°S +,, Jan, 1936, H. Womersley, ( +SAM +NN +22352, +BJR +519); 1F, Mylor, +138.77°E +, +35.05°S +, +18 Nov +, 1994, A. Austin, (QM +S 73090 +, +BJR +921); 1M, Mylor, +138.77°E +, +35.05°S +, +11 Feb +, 1979, (QM +S 73091 +, +BJR +939); 2M, 21F, 6 imm., Mylor +5km +S of, +138.77°E +, +35.05°S +, +14 Dec +, 1980, A.D. Austin, (AM +KS +10546, +BJR +686); 1F, Kanmantoo, on tree trunk, +139.00°E +, +35.07°S +, +4 Oct +, 1975, L. Davis, ( +SAM +NN +22362, +BJR +521); 1F, Clarendon, under bark, +138.63°E +, +35.12°S +, +26 Nov +, 1978, A.F. Lees, ( +SAM +NN +22348, +BJR +534); 1F, Wistow, Klenka Rd, +136.93°E +, +35.13°S +, +5 Nov +, 2003, M.S. Harvey, ( +WAM +T66946, +BJR +490); 1F, 1 imm., Wirra Wirra, +138.60°E +, +35.23°S +, +19 Sep +, 1999, Waterhouse Club, ( +SAM +NN +22350, +BJR +502); 1F, Langhome Creek, +139.03°E +, +35.30°S +, Dec, 1979, C Wilson, ( +SAM +NN +22360, +BJR +528); 1F, 1 imm., Currency Creek° +138.75°E +, +35.43°S +, +20 May +, 1986, D.C. Lee, ( +SAM +NN +22349, +BJR +533); 2M, 2F, 2 imm., Second Valley, under bark, +138.23°E +, +35.53°S +, +2 Aug +, 1992, J.M. Waldock, ( +WAM +T66944, +BJR +488); 1M, Waterfall Creek, Western River, Conservation Park, Kangaroo Is, +136.90°E +, +35.70°S +, +4 Nov +, 1987, D. Hirst, ( +SAM +NN +22370, +BJR +506); 1F, Cape Torrens Cons Park, +1km +S Kangaroo Is, +136.72°E +, +35.72°S +, +4 Nov +, 1990, E.G. Matthews, J.A. Forrest, ( +SAM +NN +22371, +BJR +532); 1F, Flinders Chase N.P. Kangaroo Is, +136.55°E +, +35.88°S +, +5 Oct +, 1994, C. Graham, ( +SAM +NN +22374, +BJR +556); 1F, Kangaroo Is., +137.33°E +, +35.92°S +, Oct, 1925, ( +SAM +NN +22369, +BJR +515); 1M, 1 imm., Rocky River camping area, Flinders Chase N.P., Kangaroo IS, under bark, +136.73°E +, +35.93°S +, +8 Nov +, 1987, D. Hirst, ( +SAM +NN +22373, +BJR +537); 1F, Rocky River camping area, Flinders Chase N.P., Kangaroo IS, under bark, +136.73°E +, +35.93°S +, +7 Nov +, 1987, D. Hirst, ( +SAM +NN +22372, +BJR +549); 1F, 1M, Naracoorte, +140.73°E +, +36.95°S +, +18 Nov +, 1978, E.G. Matthews, ( +SAM +NN +22354 5, +BJR +507); 1M, +1km +W Vic/SA border, Dukes Hwy, +140.93°E +, +36.38°S +, +7 Aug +, 1980, M.S. Harvey, ( +WAM +T66941, +BJR +489); 1F, Dingley Dell Natl Pleasure Resort, under bark, +140.68°E +, +38.03°S +, +22 Apr +, 1979, D.C. Lee, ( +SAM +NN +22357, +BJR +518). + +WESTERN +AUSTRALIA +: + +1F, Wheatley, Donnelly R Pool, +115.93°E +, +34.08°S +, +6 Jan +, 1990, J.M. Waldock, ( +WAM +T66939, +BJR +479); 1M, +1F. +7imm., Mount Barker, +117.67°E +, +34.63°S +, +1 May +, 1992, P. Man, ( +WAM +T66919, +BJR +465); 1F, Dog pool on Shannon River, +116.37°E +, +34.77°S +, +27 Apr +, 1992, M.S. Harvey, J.M. Waldock, ( +WAM +T66902, +BJR +468); 1F, +7km +N of South Coast Highway, +117.37°E +, +34.93°S +, +26 Apr +, 1992, M.S. Harvey, J.M. Waldock, ( +WAM +T66935, +BJR +476); 1F, +Denmark +, +117.35°E +, +34.95°S +, +15 Dec +, 1976, S.J. Curry, ( +WAM +T66900, +BJR +474); 1F, Walpole, +116.73°E +, +34.98°S +, +26 Apr +, 1978, S.J. Curry, ( +WAM +T66938, +BJR +477); 1F, +10km +SW of Walpole, +116.65°E +, +35.05°S +, +1 Dec. 1997 +, B. & M. Baehr, (QM +S 73110 +, +BJR +899). + + + + +FIGURES 6–13. + +Servaea incana + +. 6–9 dorsal view (6 ‘light’ female and 7 ‘dark’ female; 8 ‘light’ male and 9 ‘dark’ male); 10– 14 female genitalia (10 dorsal view of cleared holotype of + +S. incana + +, 11 ventral view of external characteristics of holotype of + +S. incana + +; 12 dorsal view of cleared lectotype of + +S. vestita + +, 13 ventral view of external characteristics of lectotype of + +S. vestita + +). Scale: total body 1 mm; remainder 0.2 mm. + + + + +FIGURES 14–22. + +Servaea incana + +(cont.) 14 known and predicted distribution; 15–20 male palp (15–17 ‘light’ male and 19–20 ‘dark’ male; 21 anterior view of geniculate male chelicera; 22 anterior view of rounded female chelicera. Scale: 0.2 mm + + + + +Diagnosis +. A large species (CL> +2.9mm +), with a very short fertilization duct. It can be separated from the smaller + +S. villosa + +by size, position of the origin of the embolus and the size and position of the accessory gland on the insemination duct, and the shape of abdominal markings. It can be separated from + +S. zabkai + +by the position of the smaller gland, which is placed terminally or subterminally on the anterior edge of the insemination duct. The insemination duct approaches the anterior edge of the epigynum, while it is nearer the centre of the epigynum in + +S. zabkai + +. The abdomen is cream to dark brown with highly variable ginger, through brown, to black markings. The distinctive dorsal central marking on the abdomen is shaped with shorter thicker arms than in + +S. villosa + +. COI sequence differs by <2% from GenBank accessions +JF949734 +-39, +JF949749 +and +JF949751 +and by>4% from all other species. + + + + +Description. Male: +Cephalothorax mid to dark orange with scattered pennate grey hairs over dorsal and lateral surfaces. Integument surrounding ALE, PME and PLE black with scattered grey hairs. Clypeus narrow, with long sparse fringe of grey hairs. Chelicerae geniculate, light to dark tan with median sparse fringe of long grey hairs. Blunt toothlike protuberance projecting forwards, three large fused promarginal teeth and one large straight fissident retromarginal tooth. Endites and labium dark brown grading to yellow. Sternum yellow to orange. Dorsal abdomen yellow to light brown with variable orange to dark brown or black pattern. Spinnerets yellow to brown. Ventral abdomen same colour as dorsal surface with faint darker median patch. Palps mid brown. L1 and L2 darker brown and more robust than L3 and L4, tibia and tarsus of L1 and L2 sparsely fringed. L3 and L4 femora with three transverse darker stripes. +Palp +: brown, tibia with single narrow apophysis. Tegulum relatively broad with anterior lateral lobe and a proximal lobe, origin of the embolus distal, forming a tapering single anticlockwise spiral around the bulb. Dimensions: CL 3.60±0.11 (20) 2.91–4.77, EFL 1.39±0.04 (20) 1.11–1.73, CW 2.88±0.10 (20) 2.30– 3.59, AEW 2.28±0.05 (20) 1.92–2.72, AMEW 1.27±0.03 (20) 1.05–1.55, PEW 2.21±0.05 (20) 1.86–2.60, AL 3.86±0.12 (12) 3.22–4.58, P1+T 1 3.49±013 (20) 2.48–4.40. + + +Female +. Cephalothorax yellow to dark orange, lower margin grading to dark brown, pars cephalica darker than pars thoracica. Integument surrounding ALE, PME and PLE black, sides with light grey hairs, scattered on the upper surface, thicker behind the PLE and on the rear surfaces. Clypeus narrow with light grey fringe of scattered hairs. Chelicerae geniculate, mid orange, with two promarginal teeth on a single base and a single, large, fissident, retromarginal tooth. Endites and labium orange grading to yellow. Sternum orange. Dorsal abdomen yellow with variable dark brown to black pattern. Spinnerets mid brown. Ventral abdomen same colour as dorsal surface with dark brown median patch. Palps mid brown. L1, L2, L3 and L4 similar sizes but grading in robustness. Legs mid brown, femur with three dark brown transverse dark bands, patella with a single transverse band, tibia with two transverse dark bands, metatarsus with two transverse bands and tarsus with a single transverse band. All bands vary in intensity between specimens. +Epigynum +: consisting of two large fossae and a lightly sclerotised margin. Rarely, a faint brown patch varying in shape is found in the middle of each fossa. Guides weakly formed and varying greatly in shape and depth. Copulatory openings indistinct. Accessory gland on the anterior edge of the insemination duct and placed either terminally or subterminally,. Insemination ducts pass laterally across the anterior part of the fossa to the mid line and then move posteriorly until entering the spermatheca on the mid line. Spermatheca large, rounded and within the margin of the fossa close to the posterior edge. Right and left insemination ducts in contact. Fertilization duct short, indistinguishable externally. +Dimensions: +CL 3.54±0.04 (55) 2.97–4.27, EFL 1.42±0.01 (54) 1.18–1.61, CW 2.81±0.03 (53) 2.29–3.34, AEW 2.28±0.02 (54) 1.98–2.54, AMEW 1.24±0.01 (54) 1.11–1.49, PEW 2.20±0.02 (54) 1.92–2.48, AL 4.58±0.13 (41) 3.41–6.19, P1+T1 2.50±0.05 (52) 1.98–2.97. + + + + +Distribution and biology. +Found in temperate regions throughout +Australia +( +Fig. 14 +). Does not extend as far inland in WA as predicted. Nocturnal, found under bark in eucalypt forest and woodlands. Likely IUCN Red List Category LC + + + + \ No newline at end of file diff --git a/data/38/61/87/386187E5FFF0FF91FF75FFECD6E24C0B.xml b/data/38/61/87/386187E5FFF0FF91FF75FFECD6E24C0B.xml new file mode 100644 index 00000000000..21dc407a58c --- /dev/null +++ b/data/38/61/87/386187E5FFF0FF91FF75FFECD6E24C0B.xml @@ -0,0 +1,310 @@ + + + +Revision of Australian jumping spider genus Servaea Simon 1887 (Aranaea: Salticidae) including use of DNA sequence data and predicted distributions + + + +Author + +Richardson, Barry J. + + + +Author + +Gunter, Nicole L. + +text + + +Zootaxa + + +2012 + +3350 + + +1 +33 + + + +journal article +10.5281/zenodo.212467 +a23093e0-d8a3-423a-8222-73ebe53836a8 +1175-5326 +212467 + + + + + + + +Servaea spinibarbis +Simon, 1909 + + + + + +Figs 39–45 + + + + + + +Servaea spinibarbis + +Simon, 1909 +: 204 + + +, +Platnick 2012 +unpaginated. + + + + + +Remarks. +All the +type +specimens examined are juveniles, though one specimen, given as male, is subadult rather than adult and palp characters are not present. The length of P1+T +1 in +this specimen is consistent with other more recent material from coastal Western +Australia +, and not consistent with + +S. melaina + + + + + +FIGURES 39–46. + +Servaea spinibarbis + +. 39–40 dorsal view (39 female, 40 male); 41–42 female genitalia (41 dorsal view of cleared specimen, 42 ventral view of external characteristics); 43–45 male palp (43 ventral view, 44 anterior lateral view, 45 posterior lateral view); 46 known and predicted distribution. Scale: total body 1 mm; remainder 0.2 mm. + + + + + +Type +material. +Syntypes +: + +3 imm. Station 115 North Fremantle +115.5°E +, +32.05°S +, ( +ZMH +, +BJR +1186); 4 imm. Station 109, Subiaco; Station 144, Buckland Hill near North Freemantle; Station 116, East Fremantle Recreation Ground; ( +ZMHB +19473, 19474, 19475,19473a). + + + +Other material examined. WESTERN +AUSTRALIA +: + +1F, Gum Tree Bay, +114.97°E +, +29.78°S +, +23 Jul +, 1995, R.P. McMillan, ( +WAM +T66905, +BJR +469); 1F, Gum Tree Bay, +114.97°E +, +29.78°S +, +10 Oct +, 1994, R.P. McMillan, ( +WAM +T66906, +BJR +470).1F, Darlington, +116.07°E +, +31.92°S +, Mar, 1975, G.H. Lowe, ( +WAM +T66957, +BJR +481); 1F, Darlington, +116.07°E +, +31.92°S +, Mar, 1975, G.H. Lowe, ( +WAM +T66957, +BJR +481); 1F, Darlington, +116.07°E +, +31.92°S +, Nov, 1968, G.H. Lowe, ( +WAM +T66956, +BJR +487); 1F,Darlington, +116.07°E +, +31.92°S +, Nov, 1968, G.H. Lowe, ( +WAM +T66956, +BJR +487); 1F, Bold Park, +115.77°E +, +31.95°S +, +2 Nov +, 1991, R.P. McMillan, ( +WAM +T66897, +BJR +466); 1F, Mosman Park, +115.77°E +, +32.02°S +, +20 Sep +, 1992, C.A. Car, ( +WAM +T66914, +BJR +446); 1F, Parmelia, +115.82°E +, +32.25°S +, +15 Oct +, 2001, A.E. de Jong, ( +WAM +T66931, +BJR +453); 1F, Parmelia, +115.82°E +, +32.25°S +, +5 Jan +, 1987, A.E. de Jong, ( +WAM +T66926, +BJR +454);. 1M, Leeuwin Swamp, Leeuwin-Naturaliste National Park, W.A., +115.08°E +, +33.87°S +, +19 August 2000 +, J. Waldock, G. Kendrick, P. Vinnnicombe, S. Sack-Smith, ( +BJR +444, +WAM +T66909). 1F, Boranup Hill, +115.03°E +, +34.15°S +, +17 Feb +, 1977, S.J. Curry, ( +WAM +, T66898, +BJR +450); 1M, Scott Rd, D’Entrecasteau National Park, W.A., +115.74°E +, +34.43°S +, +6–13 November 2003 +, Malaise Bulk Sample, Casuarina- Jarrah woodland, C. Lambkin, J. Recsei, ( +ANIC +42 0 0 0 281, +BJR +418). 1F, +Denmark +, +117.35°E +, +34.97°S +, +30 Nov +, 1987, B. and M. Baehr, (QM, +S 73111 +, +BJR +940). + + + + +Diagnosis +. It can be differentiated from + +S. incana + +, + +S. villosa + +and + +S. zabkai + +as fertilization duct is large and long and is visible externally as a deep red mass in the centre of the fossa and by the presence of a median gap between the right and left insemination ducts. It differs from + +S. narraweena + +in that the insemination duct crosses the middle of the epigynum and enters the spermatheca on the anterior edge. It can be differentiated from + +S. melaina + +as the chelicerae are light brown rather than black or dark brown, L1 is short (male P1+T1 less than 80% of CL) rather than long (male P1+T1 more than 90% of CL), the bulb is wider than the palp and the accessory gland is terminally or sub-terminally placed on the insemination duct. It is generally light brown/fawn in colour and males show female abdominal pattern rather than the male narrow stripe seen in other species. There is only a small anterior tooth projection on the brown chelicera. + + + + +Description. Male: +Cephalothorax orange with scattered pennate grey hairs over dorsal surface and lateral margins. Integument surrounding ALE, PME and PLE, black with covering of grey hairs. Clypeus narrow, with long sparse fringe of grey hairs. Chelicerae geniculate, tan. A blunt protuberance, projecting forwards off a tubercle on the anterior face of each chelicera, three large promarginal teeth on a single base and one large straight fissident retromarginal tooth. Endites tan grading to yellow with a rounded distal edge. Labium tan and sternum light brown. Abdomen with a central anterior cleft, light brown with dark brown mid line pattern, scattered spots and edges. Ventral abdomen same colour as dorsal surface of the abdomen. Spinnerets light brown. L1 and L2 more robust than L3 and L4. L1 and L2, femur, patella, tibia, metatarsus and tarsus mid brown with fringing on patella and tibia. Other legs pale yellow without fringing. All femora with three transverse darker stripes. +Palp +: brown, tibia with single slender apophysis. Tegulum relatively long and narrow without anterior lateral lobe but with a proximal lobe, bulb as wide or wider than the cymbium, origin of the embolus distal, forming a tapering single-turn anticlockwise spiral around the bulb. Dimensions: CL 2.41±0.06 (2), EFL 1.05±0.06 (2), CW 1.92 (1), AEW 1.76±0.03 (2), AMEW 0.96±0.03 (2), PEW 1.55±0.06 (2), AL 2.48 (1), P1+T1 1.89±0.09 (2). + + +Female. +Cephalothorax orange with scattered pennate grey hairs over lateral surfaces. Integument surrounding ALE, PME and PLE, black with partial covering of grey hairs. Clypeus narrow with long sparse fringe of grey hairs. Chelicerae geniculate, tan. Fang narrow in distal half. Chelicera with no protuberance projecting forwards off the anterior face, three promarginal teeth on a single base and one large straight fissident retromarginal tooth. Endites tan grading to yellow with a rounded distal edge. Labium tan grading to yellow and sternum light brown. Abdomen with a central anterior cleft, fawn with darker brown mid line pattern, scattered spots and edges. Many specimens with a large ginger ring of hairs on either side. Ventral abdomen same colour as dorsal surface of the abdomen. Spinnerets light brown. Palp yellow grading to mid brown. L1 and L2 slightly more robust than L3 and L4. L1 and L2, femur, patella, tibia, metatarsus and tarsus mid brown with sparse fringing on patella and tibia. Other legs pale yellow without fringing. All femora with three transverse darker stripes and transverse darker brown bands on the other segments. +Epigynum +: Indistinct fossae and a well sclerotised margin. A distinct brown patch varying in shape is found in the middle of each side. Guides and copulatory openings indistinct. Accessory gland either terminal or sub-terminal, on the dorsal surface of the insemination duct. Insemination duct passes laterally across the middle of the fossa to the mid line and then move posteriorly until entering the spermathecae on the anterior mid line. Spermatheca small, rounded and within the margin of the epigynum but at the posterior edge. Right and left spermatheca and insemination ducts touching. The fertilization duct is large and red in colour, arising from the dorsal anterior edge of the spermatheca, passing under the ventral edge of the insemination duct and then curving dorsally in an incomplete circle. Dimensions: CL 2.58±0.05 (11) (2.23–2.79), EFL 1.13±0.03 (11) (0.99– 1.30), CW 2.14±0.04 (11) (1.86–2.35), AEW 1.84±0.03 (11) (1.61–1.98), AMEW 1.05±0.02 (11) (0.93–1.11), PEW 1.94±0.03 (11) (1.73–2.04), AL 2.48, P1+T1 1.93±0.05 (11) (1.61–2.17). + + + + +Distribution and biology. +Found in sand areas of the coastal regions of temperate southwestern +Australia +( +Fig. 46 +). Found under bark in eucalypt forest and woodlands. Likely IUCN Red List Category LC. + + + + \ No newline at end of file diff --git a/data/38/61/87/386187E5FFF2FF9EFF75FD8FD3714BFF.xml b/data/38/61/87/386187E5FFF2FF9EFF75FD8FD3714BFF.xml new file mode 100644 index 00000000000..07135d1a79f --- /dev/null +++ b/data/38/61/87/386187E5FFF2FF9EFF75FD8FD3714BFF.xml @@ -0,0 +1,434 @@ + + + +Revision of Australian jumping spider genus Servaea Simon 1887 (Aranaea: Salticidae) including use of DNA sequence data and predicted distributions + + + +Author + +Richardson, Barry J. + + + +Author + +Gunter, Nicole L. + +text + + +Zootaxa + + +2012 + +3350 + + +1 +33 + + + +journal article +10.5281/zenodo.212467 +a23093e0-d8a3-423a-8222-73ebe53836a8 +1175-5326 +212467 + + + + + + + +Servaea narraweena + +n. sp. + + + + +Figs 31–37 + + + + +Etymology. +An arbitrary combination of letters. + + + + +Remarks +. On the basis of the structure of its genitalia and its size, the +syntype +of + +S. vestita + +from Peak Downs is an example of this species. + + + + + +Type +material. +Holotype +: + +1F, +Narraweena +, +NSW +, +149.22°E +, +35.5°S +, +20 Feb +, 1990, EP Small, (AM, +KS +30889A, +BJR +760) + + + +Paratypes +: + +1M, Pickwick Farm, S of Gunning, +149.27°E +, +34.78°S +, +1 Dec +, 1999, M +Zabka +& M Gray, (AM +KS +65912A +BJR +787.1); 2F, 4 imm, +Narraweena +, +NSW +, +149.22°E +, +35.5°S +, +20 Feb +, 1990, EP Small, (AM, +KS +30889, +BJR +760) 1F, 13 imm, +Narraweena +, +NSW +, +149.22°E +, +35.5°S +, +20 Feb +, 1990, EP Small, (AM, +KS +30890, +BJR +739) + + +Other material examined. QUEENSLAND: +1F, Peak Downs, +148.08°E +, +22.93°S +, ( +ZMH +, +BJR +1183: formerly a +syntype +of + +S. vestita + +); 1M, +10 km +NE Kaimkillenbun NE Dalby, Qld, +151.50°E +, +27.00°S +, +6 Nov +, 1990, (QM, S 73121, +BJR +930); 1F, Lake Broadwater, Qld, +151.10°E +, +27.35°S +, Aug, 1986, E. Zillman, (QM, +S 73095 +, +BJR +904); 2M, 7F, 8 imm, Lake Broadwater, Qld, +151.10°E +, +27.35°S +, +28 Jul +, 1982, M. Bennie, (QM, +S 61147 +, +BJR +917); 2F, Lake Broadwater, Qld, +151.10°E +, +27.35°S +, +28 Jul +, 1982, M. Bennie, (QM, +S 61147 +, +BJR +917.2). + +NEW + +SOUTH +WALES + +: + +1M, 2 imm, Agnes Banks, +150.68°E +, +33.62°S +, +19 Sep +, 1965, RE Mascord, (AM, +KS +18940, +BJR +690); 1M, Frazer Res Wahroonga, +151.13°E +, +33.72°S +, +8 Oct +, 1996, J Noble, (AM, +KS +56507, +BJR +773);. +AUSTRALIAN CAPITAL TERRITORY: +1F Ginninderra Experimental Orchard, +ACT +, +149.03°S +, +35.22°E +, +30 Jan +, 1965, ( +ANIC +, 42 0 0 0 290, +BJR +427); 1F, Westwood, Canberra, +ACT +, +149.13°E +, +35.30°S +, +5 Mar +, 1972, E. MacCallan, (QM, +S 73093 +, +BJR +928). +VICTORIA: +1F, Bundoora, La Trobe University, Acacia, +145.07°E +, +37.70°S +, +19 Sep +, 1981, (QM, +S 61146 +, +BJR +919); 1M, Clayton, Monash University, Vic, Peridomestic, +145.13°E +, +37.92°S +, +19 Oct +, 1980, M.S. Harvey, ( +WAM +, T66950, +BJR +493). + +SOUTH +AUSTRALIA +: + +2F, Maculta, nr Angaston, SA, On tree trunk, +139.05°E +, +34.5°S +, +9 Jul +, 1979, D.I. Lang, ( +SAM +, +NN +223678, +BJR +529); 1M, 5F, Para Hills, SA, on flowering plants, +138.65°E +, +34.80°S +, +11 Sep +, 1975, G. Crook, ( +SAM +, +NN +223317, +BJR +514); 1F, Uraidla, SA, +138.75°E +, +34.95°S +, +21 Dec +, 1994, J.M. Waldock, ( +WAM +, T66945, +BJR +495); 1F, Belair National Park, SA, +138.65°E +, +35.03°S +, +9 Feb +, 1936, H. Womersley, ( +SAM +, +NN +22351, +BJR +527); 1M, Aldinga Scrub Cons. Park, SA, +138.48°E +, +35.28°S +, +16 Jun +, 1987, E.G. Matthews, J.A. Forrest, ( +SAM +, +NN +22340, +BJR +543); 1F, Nappyalla, SE Longhorn Creek, SA, +139.12°E +, +35.33°S +, Dec, 1992, J. Eckert, ( +SAM +, +NN +22359, +BJR +546), 1F, 3 imm, Hindmarsh Is, Goolwa, SA, under bark, +138.87°E +, +35.52°S +, +7 Sep +, 1975, A.F. Lees, Hilton, ( +SAM +, +NN +22358, +BJR +547). + + + + +FIGURES 31–38. + +Servaea narraweena + +n. sp. +31–32 dorsal view (31 female, 32 male); 33–34 female genitalia (33 dorsal view of cleared specimen, 34 ventral view of external characteristics); 35–37 male palp (35 ventral view, 36 anterior lateral view, 37 posterior lateral view); 38 known and predicted distribution. Scale: total body 1 mm; remainder 0.2 mm. + + + + +Diagnosis. +It can be differentiated from + +S. incana + +, + +S. villosa + +and + +S. zabkai + +as fertilization duct is large and long and is visible externally as a deep red mass in the centre of the fossa and by the presence of a median gap between right and left insemination ducts. It can be differentiated from + +S. melaina + +and + +S. spinibarbis + +as the insemination duct approaches the anterior edge of the epigynum and enters the spermatheca towards the posterior edge. + + + + +Description. Male: +Cephalothorax dark orange with scattered pennate grey hairs over dorsal surface and lateral surfaces. Integument surrounding ALE, PME and PLE, black with scattered grey hairs. Clypeus narrow, with long sparse fringe of grey hairs. Chelicerae geniculate, tan. No toothlike protuberance projecting forwards, four large fused promarginal teeth and one large straight fissident retromarginal tooth. Endites light brown grading to yellow with a slight protuberance on the distal edge. Labium brown and sternum orange. Abdomen with a central anterior cleft, cream with two dark brown parallel mid line stripes and associated patterning, striped pattern on the margins. Ventral abdomen same colour as dorsal surface of the abdomen on the sides with a darker median area. Spinnerets same colour as abdomen. L1 and L2 darker brown and more robust than L3 and L4, tibia and metatarsus sparsely fringed. L3 and L4 femora with three transverse darker stripes. +Palp +: brown, tibia with single slender apophysis. Tegulum relatively broad with anterior lateral lobe and a proximal lobe, origin of the embolus distal, forming a tapering single anticlockwise spiral around the bulb. Dimensions CL 2.52±0.05 (7) 2.35–2.66, EFL 1.00±0.03 (7) 0.87–1.11, CW 1.95±0.04 (7) 1.80–2.04, AEW 1.77±0.02 (7) 1.67–1.86, AMEW 1.00±0.01 (7) 0.93–1.05, PEW 1.72±0.03 (7) 1.61–1.80, P1+T1 2.49±0.08 (7) 2.17–2.72. + + + +Female ( +Holotype +): + +Cephalothorax dark orange, its lower margin grading to dark brown. Integument surrounding ALE, PME and PLE, black, covered with light grey hairs, scattered on the upper surface, thicker behind the PLE and on the rear surfaces. Clypeus narrow with light grey fringe of scattered hairs. Chelicerae geniculate, tan, with three promarginal teeth on a single base and a single, large, fissident, retromarginal tooth. Endites and labium mid brown grading to yellow. Sternum yellow. Dorsal abdomen yellow with variable brown pattern. Spinnerets mid brown. Ventral abdomen same colour as dorsal surface with dark brown median patch. Palps yellow grading distally to mid brown. L1, L2 and L3 similar sizes and finely built. L4 similar but longer. Legs yellow grading distally to mid brown, femur with three dark brown transverse dark bands, patella with a single transverse band, tibia with two transverse dark bands and metatarsus with two transverse bands and tarsus with a single transverse band. +Epigynum +: consisting of two large fossae and a lightly sclerotised margin. Rarely, a faint brown patch varying in shape is found in the middle of each fossa. Guides and copulatory openings indistinct. Accessory gland either terminally or in the distal third, on the dorsal surface of the insemination duct. Insemination duct passes laterally across the middle of the fossa to the mid line and then moves posteriorly until entering the spermatheca on the posterior mid line. Spermatheca small, rounded and within the margin of the fossa but at the posterior edge. Right and left spermatheca and insemination ducts often in contact. The fertilization duct is large, dark reddishbrown, arising from the ventral anterior edge of the spermatheca and curving in an incomplete circle below the ventral surface of the insemination duct before moving dorsally, clearly distinguishable externally. +Dimensions: +CL 2.58±0.07 (9) 2.33–2.97, EFL 1.07±0.02 (9) 0.93–1.18, CW 2.08±0.0.05 (9) 1.86–2.35, AEW 1.82±0.0.03 (9) 1.67–1.98, AMEW 1.05±0.02 (9) 0.99–1.11, PEW 1.89±0.04 (9) 1.67–2.04, P1+T1 1.90±0.05 (9) 1.67–2.20. + + + + +Distribution and biology. +Found in temperate regions of eastern +Australia +from central Queensland to Adelaide; not in Tasmania ( +Fig. 38 +). Found on the coastal side of the Great Dividing Range of SE +Australia +, but not in the inland districts as predicted. Nocturnal, found under bark in eucalypt forest and woodlands. Likely IUCN Red List Category LC. + + + + \ No newline at end of file diff --git a/data/38/61/87/386187E5FFF7FF9CFF75FE5FD020495B.xml b/data/38/61/87/386187E5FFF7FF9CFF75FE5FD020495B.xml new file mode 100644 index 00000000000..ecd27aae81e --- /dev/null +++ b/data/38/61/87/386187E5FFF7FF9CFF75FE5FD020495B.xml @@ -0,0 +1,470 @@ + + + +Revision of Australian jumping spider genus Servaea Simon 1887 (Aranaea: Salticidae) including use of DNA sequence data and predicted distributions + + + +Author + +Richardson, Barry J. + + + +Author + +Gunter, Nicole L. + +text + + +Zootaxa + + +2012 + +3350 + + +1 +33 + + + +journal article +10.5281/zenodo.212467 +a23093e0-d8a3-423a-8222-73ebe53836a8 +1175-5326 +212467 + + + + + + + +Servaea melaina + +n.sp. + + + + +Figs 23–29 + + + + +Etymology. +From μελας =dark, referring to an easily discernable difference from + +S. spinibarbis + +. + + + +FIGURES 23–30. + +Servaea melaina + +n. sp. +23–24 dorsal view (23 female, 24 male); 25–26 female genitalia (25 dorsal view of cleared specimen, 26 ventral view of external characteristics); 27–29 male palp (27 ventral view, 28 anterior lateral view, 29 posterior lateral view); 30 known and predicted distribution. Scale: total body 1 mm; remainder 0.2 mm + + +Remarks. + + + + +Type +material. +Holotype +: + +1F, Mount Barker, +WA +, +117.67°E +, +34.63°S +, +1 May +, 1992, P.J. +Mann +, ( +WAM +T +100348 +, +BJR +465A). + + + +Paratype +: + +1M, Mount Barker, 19 Osborne Rd, +WA +, peridomestic, +117.67°E +, +34.63°S +, Dec, 1992, P.J. +Mann +, ( +WAM +, T66917, +BJR +440); 1M, Mount Barker, 19 Osborne Rd, +WA +, +117.67°E +, +34.63°S +, Dec, 1992, P.J. +Mann +, ( +WAM +, T66918, +BJR +443). + + + +Other material examined. WESTERN +AUSTRALIA +: + +1M, Pinnaroo Valley Memorial Park, +115.77°E +, +31.80°S +, +1 Aug +, 1993, D. Leary, ( +WAM +T66932, +BJR +460); 1F, Trigg, +115.75°E +, +31.87°S +, +6 Sep +, 1988, D. Knowles, ( +WAM +, T66937, +BJR +483); 1M, Trigg, +115.75°E +, +31.87°S +, +6 Sep +, 1988, D. Knowles, ( +WAM +, T66936, +BJR +484); 1F, Karrinyup Shopping Centre, +115.77°E +, +31.88°S +, +28 Aug +, 1992, J. Waldock, ( +WAM +, T66907, +BJR +451); 1M, East Guildford, 28 Swan St, +115.98°E +, +31.90°S +, +8 Sep +, 1999, P. Vinnicombe, G.W. Kendrick, ( +WAM +, T66903, +BJR +475); 1F, Mount Lawley, +115.87°E +, +31.92°S +, +30 Nov +, 1986, J. Waldock, D. Terry, ( +WAM +, T66920, +BJR +445); 1F, Maylands, peridomestic, +115.88°E +, +31.93°S +, +17 Feb +, 1990, J. Waldock, ( +WAM +, T66910, +BJR +439); 1M, Perth, outside Museum, +115.85°E +, +31.95°S +, +11 Oct +, 1999, M.S. Harvey, J.M. Waldock, ( +WAM +T66933, +BJR +485); 1F, Nedlands, Edward St, +115.80°E +, +31.98°S +, +27 Nov +, 1996, A. Baynes, ( +WAM +, T66922, +BJR +452); 1F, Nedlands, Edward St, +115.80°E +, +31.98°S +, +17 Dec +, 1990, A. Baynes, ( +WAM +, T66924, +BJR +456); 1F, Nedlands, Edward St, +115.80°E +, +31.98°S +, +26 Sep +, 1991, A. Baynes, ( +WAM +, T66923, +BJR +459); 1M, Yangebup, +115.82°E +, +32.12°S +, +22 Aug +, 1996, D. Mead-Hunter, ( +WAM +, T66940, +BJR +486); 1M, Parmelia, +115.82°E +, +32.25°S +, +11 Oct +, 1986, A.E. de Jong, ( +WAM +, T66925, +BJR +463); 1M, Parmelia, +115.82°E +, +32.25°S +, +11 Sept +, 1996, A.E. de Jong, ( +WAM +, T66929, +BJR +457); 1M, Parmelia, +115.82°E +, +32.25°S +, +11 Sep +, 1989, A.E. de Jong, ( +WAM +, T66927, +BJR +462); 1M, Parmelia, +115.82°E +, +32.25°S +, +26 May +, 1997, A.E. de Jong, ( +WAM +, T66930, +BJR +461); 1M, Parmelia, +115.82°E +, +32.25°S +, +6 Nov +, 1990, A.E. de Jong, ( +WAM +, T66928, +BJR +455); 1M, Furnissdale, SE Mandurah, +115.77°E +, +32.57°S +, +24 Aug +, 1991, F.H. Uther +Baker +, ( +WAM +, T66904, +BJR +467); 2F, Sandy Hook Is, Recherche Archipelago, Litter, 122°E, +34.03°S +, +16 Nov +, 1998, J..M. Waldock, ( +WAM +, T66934, +BJR +478); 1M, Mockerdillup Rd, +15km +SW Bridgetown, +116.10°E +, +34.10°S +, +11 Dec +, 1986, D. Terry, ( +WAM +, T66912, +BJR +447); 1M, Mockerdillup Rd, +15km +SW Bridgetown, +116.10°E +, +34.10°S +, +1 Nov +, 1986, J. Waldock, D.Terry, ( +WAM +, T66911, +BJR +449); 2F, +1km +N Boyup/Franklin Rds jn, W of Cranbrook, +117.55°E +, +34.30°S +, +18 Nov +, 1992, A.F. Longbottom, ( +WAM +, T66899, +BJR +464); 1M, 1 imm, Stirling Range N.P., Stirling Range Rd, Open woodland, +118.05°E +, +34.35°S +, +3 Nov +, 2003, R. Oberprieler, ( +ANIC +, 42 0 0 1480, +BJR +1173); 2F, 1 imm, Mount Barker/Porogurups Rd, +117.80°E +, +34.68°S +, +16 Feb +, 1993, A.F. Longbottom, ( +WAM +, T66916, +BJR +473); 1M, +6.5 miles +W of +Denmark +, +117.23°E +, +34.97°S +, +29 Dec +, 1962, J. Crawley, ( +WAM +, T66901, +BJR +472). + + + + +Diagnosis. +It can be differentiated from + +S. incana + +, + +S. villosa + +and + +S. zabkai + +as the fertilization duct is large and long and is visible externally as a deep red mass in the centre of the fossa and by the presence of a median gap between right and left insemination ducts. It differs from + +S. narraweena + +as the insemination duct crosses the middle of the epigynum and enters the spermatheca on the anterior edge and from + +S. spinibarbis + +as the chelicerae are black or dark brown rather than light brown, L1 is long (P1+T1 more than 90% of CL) rather than short (P1+T1 less than 80% of CL), the bulb is narrower than the palp and the accessory gland is towards the middle of the insemination duct rather than terminal or sub-terminal. + + + + +Description. Male: +Cephalothorax dark orange covered with pennate grey hairs over dorsal surface and lateral surfaces. Integument surrounding ALE, PME and PLE, black with thick covering of grey hairs. Clypeus narrow, with long sparse fringe of grey hairs. Chelicerae geniculate, black grading distally to dark tan. A toothlike protuberance, projecting forwards off a tubercle on the anterior face of each chelicera, three large promarginal teeth on a single pediment and one large straight fissident retromarginal tooth. Endites dark tan grading to yellow with a protuberance on the distal edge. Labium black and sternum mid brown. Abdomen without a central anterior cleft, mid brown with dark brown mid line stripe and patterning that stretches to the margins. Ventral abdomen same colour as dorsal surface of the abdomen on the sides with a darker median stripe and with scattered white patches of guanine. Spinnerets mid brown. L1 and L2 more robust than L3 and L4. All femoras, patellae, tibiae yellow, tarsi and metatarsi mid brown without fringing.. L3 and L4 femora with three transverse darker stripes, L1 and L2 plane. +Palp +: brown, tibia with single fine apophysis. Tegulum relatively broad with anterior lateral lobe and a proximal lobe, origin of the embolus distal, forming a tapering single anticlockwise spiral around the bulb. Dimensions: CL 2.65±0.05 (12) 2.35–2.91, EFL 1.05±0.03 (12) 0.87–1.24, CW 2.05±0.04 (12) 1.80–2.29, AEW 1.85±0.04 (12) 1.67–2.04 AMEW 1.04±0.02 (12) 0.93–1.11, PEW 1.81±0.04 (12) 1.61–2.04, P1+T +1 2. 74 +±0.10 (11) 2.17–3.22. + + + +Female ( +Holotype +): + +Cephalothorax dark orange covered with pennate grey hairs over dorsal surface and lateral surfaces. Integument surrounding ALE, PME and PLE, black with thick covering of grey hairs. Clypeus narrow, with long sparse fringe of grey hairs. Chelicerae geniculate, black grading distally to dark tan with four promarginal teeth on a single base and a single, large, fissident, retromarginal tooth but no protuberance on the front face. Endites and labium mid brown. Sternum yellow. Abdomen without a central anterior cleft, mid brown with dark brown mid line stripe of variable intensity and patterning that stretches to the margins. Ventral abdomen same colour as dorsal surface of the abdomen on the sides with a darker median stripe. Spinnerets mid brown. Ventral abdomen same colour as dorsal surface of the abdomen on the sides with a darker median stripe and with scattered white patches of guanine. Palps yellow. L1, L2 and L3 similar sizes with a slender build. L4 similar but longer. Legs yellow grading distally to mid brown, femur without three dark brown transverse bands, patella with a single transverse brown band, tibia with two transverse brown bands, metatarsus with two transverse bands and tarsus with a single transverse band. +Epigynum +: consisting of two large fossae and a sclerotised margin. A distinct brown patch varying in shape is found in the middle of each fossa. Guides and copulatory openings indistinct. Accessory gland either terminally or in the distal third, on the dorsal surface of the insemination duct. Insemination duct passes laterally across the middle of the fossa to the mid line and then moves posteriorly until entering the spermatheca on the anterior mid line. Spermatheca small, rounded and within the margin of the fossa but at the posterior edge. Right and left spermatheca and insemination ducts well separated. The fertilization duct is large, arising from the ventral anterior edge of the spermatheca and curving dorsally in an incomplete circle ( +Fig. 25 +). +Dimensions +: +Holotype +, CL 2.85, EFL 1.11, CW 2.23, AEW 1.86, AMEW 0.99, PEW 1.91, AL 3.10, L1 4.76 (1.42+0.80+0.99+0.0.99+0.56), L2 4.20 (1.30+0.74+0.93+0.0.80+0.43), L3 4.45 (1.61+0.80+0.87+0.74+0.43), L4 5.38 (1.73+0.80+1.05+1.30+0.50): General, CL 2.58±0.07 (9) 2.32–2.97, EFL 1.07±0.02 (9) 0.93–1.18, CW 2.08±0.05 (9) 1.86–2.35, AEW 1.82±0.03 (9) 1.67–1.98, AMEW 1.05±0.02 (9) 0.99–1.11, PEW 1.89±0.04 (9) 1.67–2.04, P1+T1 1.90±0.05 (9) 1.67–2.20. + + + + +Distribution and biology. +Found in south-western +Australia +( +Fig. 30 +) on non-sandy soils, surprisingly also found in the Swan River valley sympatric with + +S. spinibarbis + +. Found under bark in eucalypt forest and woodlands. Likely IUCN Red List Category LC. + + + + \ No newline at end of file diff --git a/data/38/61/87/386187E5FFF8FF96FF75FADAD6B749D3.xml b/data/38/61/87/386187E5FFF8FF96FF75FADAD6B749D3.xml new file mode 100644 index 00000000000..3b97434a15f --- /dev/null +++ b/data/38/61/87/386187E5FFF8FF96FF75FADAD6B749D3.xml @@ -0,0 +1,93 @@ + + + +Revision of Australian jumping spider genus Servaea Simon 1887 (Aranaea: Salticidae) including use of DNA sequence data and predicted distributions + + + +Author + +Richardson, Barry J. + + + +Author + +Gunter, Nicole L. + +text + + +Zootaxa + + +2012 + +3350 + + +1 +33 + + + +journal article +10.5281/zenodo.212467 +a23093e0-d8a3-423a-8222-73ebe53836a8 +1175-5326 +212467 + + + + + + + +Servaea obscura +Rainbow 1915 + + + + + + + + +Servaea obscura +Rainbow 1915 + +791, pl. 68 +Fig. 22 + + + + + +Type +material. +Syntypes + +: 1sub-adult F 1 imm +SAM +Flat Rock Hole, Musgrave Ranges; +26° 33’S +132° 26’E +, July, 1914, Capt. S.A. White Expedition 1915 ( +BJR +559, +NN +418). + + + + +Remarks: +Based on immature specimens in poor condition, does not belong in + +Servaea + +. + + + + \ No newline at end of file diff --git a/data/38/61/87/386187E5FFFBFF96FF75F8F7D08E4E58.xml b/data/38/61/87/386187E5FFFBFF96FF75F8F7D08E4E58.xml new file mode 100644 index 00000000000..d3caa73c767 --- /dev/null +++ b/data/38/61/87/386187E5FFFBFF96FF75F8F7D08E4E58.xml @@ -0,0 +1,165 @@ + + + +Revision of Australian jumping spider genus Servaea Simon 1887 (Aranaea: Salticidae) including use of DNA sequence data and predicted distributions + + + +Author + +Richardson, Barry J. + + + +Author + +Gunter, Nicole L. + +text + + +Zootaxa + + +2012 + +3350 + + +1 +33 + + + +journal article +10.5281/zenodo.212467 +a23093e0-d8a3-423a-8222-73ebe53836a8 +1175-5326 +212467 + + + + + + + +Servaea zabkai + +n. sp. + + + + +Figs 55–58 + + + + +Etymology. +Named for the collector of the +type +specimens and doyen of Australian salticid taxonomists, Prof. Marek +Zabka +. + + + + +FIGURES 55–58. + +Servaea zabkai + +n. sp. +55 dorsal view (female); 55–57 female genitalia (56 dorsal view of cleared specimen, 57 ventral view of external characteristics); 58 known distribution. Scale: total body 1 mm; remainder 0.2 mm. + + + + + +Type +material. +Holotype +: + +1F, Atherton area, +145.48°E +, +17.27°S +, +18 Oct +, 2002, M. +Zabka +, (AM +KS +81340, +BJR +815). + + + +Paratype +. + +1F, Atherton area, +145.48°E +, +17.27°S +, +18 Oct +, 2002, M. +Zabka +, (AM +KS +81339, +BJR +830). +Diagnosis. +This is a large species (CL> +2.9mm +) with a very short fertilization duct. It can be separated from the smaller + +S. villosa + +by size and abdominal markings, and from + +S. incana + +by the position of the much larger accessory gland on the dorsal surface of the insemination duct, in which it resembles + +S. narraweena + +. The spermatheca are anterior to and well separated from the posterior edge of the epigynum. +COI +sequence differs by <2% from GenBank accession +JF949750 +and by>4% from other + +Servaea + +species. + + + + + +Description. Female ( +Holotype +): + +Cephalothorax dark orange dorsally and dark brown on the sides, pars cephalica darker than pars thoracica. Integument surrounding ALE, PME and PLE black, dorsal surface covered with fine dark brown hairs, sides and rear covered with large, pennate grey hairs. Clypeus narrow with occasional long, light grey hairs. Chelicerae broad, rounded and geniculate, mid orange, with sparse grey hairs on the anterior mid line. Three small promarginal protuberances on a single base and a single, large, fissident, retromarginal tooth. Endites and labium mid orange grading to yellow. Sternum orange. Dorsal abdomen brown with variable dark brown pattern. Spinnerets mid brown. Ventral abdomen same colour as dorsal surface with dark brown median patch. Palps mid brown. L1, L2, L3 and L4 similar in size and relatively slender. Legs mid brown, femur with three dark brown transverse dark bands, patella with a single transverse band, tibia with two transverse dark bands and metatarsus with one transverse band and tarsus without a transverse band. +Epigynum: +Consists of two large fossae with lightly sclerotised margins. Guides weakly formed. Copulatory openings indistinct. Accessory gland in the centre of the dorsal surface and in the distal third of the insemination duct. Insemination duct passes laterally across the mid part of the fossa to the mid line and then move posteriorly until entering the spermatheca on the mid line. Spermatheca large, rounded and well forward of the posterior margin of the fossa. Right and left insemination ducts in contact. Fertilization duct short. +Dimensions: +CL 3.47, EFL 1.42, CW 2.85, AEW 2.23, AMEW 0.99, PEW 2.23, AL 3.72, P1+T1 2.47, L1 6.44 (1.98+1.30+1.36+1.18+0.62), L2 6.00 (1.92+1.11+1.30+1.11+0.56), L3 6.13 (1.92+0.99+1.24+1.36+0.62), L4 7.06 (2.17+1.05+1.55+1.67+0.62). + + + + +Distribution. +Known only from two specimens from the Atherton tableland of northern Queensland ( +Fig. 58 +). Likely IUCN Red List Category VU B1ab(iii) + + + + \ No newline at end of file diff --git a/data/38/61/87/386187E5FFFFFF95FF75F8BFD13D4CC3.xml b/data/38/61/87/386187E5FFFFFF95FF75F8BFD13D4CC3.xml new file mode 100644 index 00000000000..c257fbf946c --- /dev/null +++ b/data/38/61/87/386187E5FFFFFF95FF75F8BFD13D4CC3.xml @@ -0,0 +1,1337 @@ + + + +Revision of Australian jumping spider genus Servaea Simon 1887 (Aranaea: Salticidae) including use of DNA sequence data and predicted distributions + + + +Author + +Richardson, Barry J. + + + +Author + +Gunter, Nicole L. + +text + + +Zootaxa + + +2012 + +3350 + + +1 +33 + + + +journal article +10.5281/zenodo.212467 +a23093e0-d8a3-423a-8222-73ebe53836a8 +1175-5326 +212467 + + + + + + + +Servaea villosa +( +Keyserling, 1881 +) + + + + + +Figs 1 +, +47–53 + + + + + + +Hasarius villosus + +Keyserling, 1881 +: 1281 + + +, pl. 109 +Fig. 5 +(on plate; +6 in +text) + +Servaea villosa +: + +Zabka 1991 +: 52 + + +, +Platnick 2012 +unpaginated + + + + + +Remarks. +The species is highly variable in size, colouring, hairiness and patterning. Specimens of the variation in abdominal patterning are shown in +Fig. 1 + + + + +Material examined. QUEENSLAND +: 1F, Eurimbula SE of Gladstone, +151.83°E +, +24.18°S +, +1 Mar +, 1975, C. Horseman, (AM +KS +6928 +BJR +676); 1F, Eurimbula SE of Gladstone, +151.83°E +, +24.18°S +, +1 Mar +, 1975, C. Horseman, (AM +KS +261 +BJR +693); 1M, 7 imm., Kroombit Tops, Lower Dry Creek, +45km +SSW Calliope, +151.05°E +, +24.37°S +, +9 Dec +, 1983, V. Davies, J. Gallon, (QM +S 73089 +BJR +943); 1F, Bulburin Forestry Nursery NW of Bundaberg, +151.48°E +, +24.52°S +, +1 Mar +, 1975, M. Gray C. Horseman, (AM +KS +104 +BJR +575); 2M, 5F, Bunyobi, Hunsley Rd, Kidaman Creek, +152.78°E +, +26.63°S +, +1 Jul +, 2010, R. Whyte, (QM +BJR +1128); 2M, Bunyobi, Hunsley Rd, Kidaman Creek, +152.78°E +, +26.63°S +, +10 May +, 2010, R. Whyte, ( +ANIC +42 0 0 1496 +BJR +1130); 2M, Taylors residence, Lochinvar +WBR +, +152.95°E +, +27.45°S +, +15 Jun +, 2010, R. Whyte, ( +ANIC +42 0 0 1493 +BJR +1129); 1F, The +Island +, Walton Bridge Reserve, The Gap, +152.95°E +, +27.45°S +, +27 Aug +, 2009, R. Whyte, ( +ANIC +42 0 0 1494 +BJR +1131); 1F, 917 Waterworks Rd, The Gap, +152.95°E +, +27.45°S +, +27 Aug +, 2009, R. Whyte, ( +ANIC +42 0 0 1497 +BJR +1187); 3M, 3F, 1 imm, Paten Rd, The Gap, +152.95°E +, +27.45°S +, +29 Aug +, +Jan 2011 +, R. Whyte, ( +ANIC +42 0 0 1498 +BJR +1188); 2M, 4 imm. Brisbane, +153.02°E +, +27.47°S +, +23 Jan +, 1983, V. Davies, (QM S 73107 +BJR +956); 2F, 4 imm., Upper Brookfield,, +152.87°E +, +27.48°S +, +11 Dec +, 1980, V. Davies, R. Raven, (QM +S 73083 +BJR +916); 1M, 1 imm., Upper Brookfield, +152.87°E +, +27.48°S +, +15 Oct +, 1980, V. Davies, R. Raven, (QM +S 73078 +BJR +925); 1F, 6 imm., Upper Brookfield,, +152.87°E +, +27.48°S +, +17 Jul +, 1981, V. Davies, R. Raven, (QM S 73106 +BJR +958); 1M, 2F, Brookfield, +152.92°E +, +27.50°S +, +15 Feb +, 1981, Y. Lubin, (QM +S 73081 +BJR +937); 1F, Causeway Lagoon, Mining Company Road, +153.53°E +, °S, 27.52, +11 Oct +, 2009, R. Whyte, ( +ANIC +42 0 0 1495 +BJR +1132). + +NEW + +SOUTH +WALES + + +: 1F, Wild Cattle Creek Forest, +152.70°E +, +30.15°S +, +15 Nov +, 1982, J.T. Doyen, ( +ANIC +42 0 0 0 299 +BJR +436); 1M, Bellingen, The +Island +, +152.90°E +, +30.45°S +, +3 Aug +, 1981, M. Gray, (AM +KS +9429 +BJR +563); 1M, Irishman SF, Rickerbys Rd, +1km +from jnct Bellbucca Rd, +152.70°E +, +30.55°S +, +25 Nov +, 1999, M. Gray, G. Milledge & H. Smith, (AM +KS +65873 +BJR +808); 1F, 3 imm., Turners Dip, +152.70°E +, +31.02°S +, +22 Nov +, 1978, R. Raven, (QM +S 73082 +BJR +936); 1M, Port +Macquarie +, +152.92°E +, +31.42°S +, +10 Jan +, 2005, A. Walker, ( +ANIC +42 0 0 0 242 +BJR +1127); 1F, Port +Macquarie +, Sea Acres Nature Reserve, +152.93°E +, +31.47°S +, +28 Feb +, 1999, G. Williams, (AM +KS +56324 +BJR +737); 1M, Port +Macquarie +, Sea Acres Nature Reserve, +152.93°E +, +31.47°S +, +28 Feb +, 1999, G. Williams, (AM +KS +56329 +BJR +777); 1M, Camden Head, +152.83°E +, +31.65°S +, +1 Apr +, 2000, G. & T. Williams, (AM +KS +62199 +BJR +816); 1F, ‘Lorien’ Wildlife Refuge +3 km +N of Lansdowne, +152.57°E +, +31.77°S +, +26 Nov +, 1987, D.J. Bickel, (AM, +KS +29831 +BJR +717); 1M, Cobark Forest Park, Barrington Tops, +151.60°E +, +31.90°S +, +11 Feb +, 1984, I.D. Naumann, ( +ANIC +42 0 0 0 283 +BJR +420); 1F, Munmorah NP, +151.57°E +, +33.22°S +, +11 Dec +, 2002, M. Gray, (AM +KS +81976 +BJR +826); 1M, 2 imm., The Basin, Pittwater, +151.28°E +, +33.60°S +, +5 Jul +, 1966, R.E. Mascord, (AM +KS +18343 +BJR +564); 1F, Coasters Retreat, +151.30°E +, +33.60°S +, +29 Jan +, 1967, R.E. Mascord, (AM +KS +22262 +BJR +761); 1M, Mt Colah, +151.12°E +, +33.67°S +, +28 Aug +, 1988, M.R. Gray, (AM +KS +19445 +BJR +766); 1M, Dural, +151.03°E +, +33.68°S +, +28 Nov +, 1993, J. Noble, (AM +KS +56529 +BJR +713); 1F, Hornsby, Waitara Creek, +151.08°E +, +33.70°S +, +30 Sep +, 2000, G. Milledge, (AM +KS +68253 +BJR +788); 1M, Hornsby, Waitara Creek, +151.08°E +, +33.70°S +, +14 Apr +, 2001, G. Milledge, (AM +KS +71254 +BJR +790); 1F, Hornsby, Waitara Creek., +151.08°E +, +33.70°S +, +16 Oct +, 2000, G. Milledge, (AM +KS +68560 +BJR +797); 2M, Waitara Ck, Hornsby, +151.08°E +, +33.70°S +, +22 Sep +, 2002, G. Milledge, (AM +KS +79675 +BJR +831); 1M, Frazer Reserve, Wahroonga, +151.13°E +, +33.72°S +, +20 Aug +, 1997, J. Noble, (AM +KS +51395 +BJR +705); 1M, Frazer Reserve, Wahroonga, +151.13°E +, +33.72°S +, +8 Oct +, 1996, J. Noble, (AM +KS +56502 +BJR +738); 1F, Beecroft, +151.05°E +, +33.73°S +, +30 May +, 2004, J. Noble, (AM +KS +90876 +BJR +714); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +26 Oct +, 1997, J. Noble, (AM +KS +51449 +BJR +694); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +4 Aug +, 1997, J. Noble, (AM +KS +52001 +BJR +697); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +9 Dec +, 1992, J. Noble, (AM +KS +56448 +BJR +698); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +9 Jan +, 1997, J. Noble, (AM +KS +51658 +BJR +700); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +4 Jan +, 1997, J. Noble, (AM +KS +51662 +BJR +701); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +30 Apr +, 1997, J. Noble, (AM +KS +52004 +BJR +709); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +17 Sep +, 1993, J. Noble, (AM +KS +56484 +BJR +710); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +9 Aug +, 1993, J. Noble, (AM +KS +58538 +BJR +711); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +30 Apr +, 1997, J. Noble, (AM +KS +52003 +BJR +712); 1M, Beecroft, +151.07°E +, +33.75°S +, +5 Oct +, 1992, J. Noble, (AM +KS +58571 +BJR +715); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +30 May +, 1999, J. Noble, (AM +KS +58971 +BJR +718); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +9 Oct +, 1992, J. Noble, (AM +KS +56441 +BJR +719); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +30 Apr +, 1999, J. Noble, (AM +KS +56388 +BJR +721); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +9 Aug +, 1993, J. Noble, (AM +KS +56487 +BJR +722); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +4 Aug +, 1997, J. Noble, (AM +KS +52002 +BJR +723); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +15 Aug +, 1993, J. Noble, (AM +KS +58536, ( +BJR +724); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +10 Oct +, 1996, J. Noble, (AM +KS +58506 +BJR +725); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +9 Aug +, 1993, J. Noble, (AM +KS +56436 +BJR +726); 1M Beecroft Reserve, +151.07°E +, +33.75°S +, +22 Aug +, 1995, J. Noble, (AM +KS +56511 +BJR +731); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +14 Jul +, 1999, J. Noble, (AM +KS +58970 +BJR +732); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +10 Oct +, 1996, J. Noble, (AM +KS +58507 +BJR +733); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +9 Aug +, 1993, J. Noble, (AM +KS +56478 +BJR +741); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +9 May +, 1993, J. Noble, (AM +KS +56485 +BJR +742); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +15 Aug +, 1993, J. Noble, (AM +KS +58542 +BJR +743); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +9 Aug +, 1993, J. Noble, (AM +KS +56481 +BJR +744); 1F, Beecroft Reserve, 151.07, °E, +33.75°S +, +10 Oct +, 1996, J. Noble, (AM +KS +58505 +BJR +748); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +8 Mar +, 1992, J. Noble, (AM +KS +34409 +BJR +764); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +22 Dec +, 1992, J. Noble, (AM +KS +56440 +BJR +771); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +30 Sep +, 1995, J. Noble, (AM +KS +56517 +BJR +774); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +5 Oct +, 1999, J. Noble, (AM +KS +56411 +BJR +775); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +17 Nov +, 1992, J. Noble, (AM +KS +56442, +BJR +781); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +25 Jul +, 2001, J. Noble, (AM +KS +76828 +BJR +784); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +25 Jul +, 2001, J. Noble, (AM +KS +76823 +BJR +789); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +25 Jul +, 2001, J. Noble, (AM +KS +76829 +BJR +793); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +25 Jul +, 2001, J. Noble, (AM +KS +76830 +BJR +795); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +20 Aug +, 1999, J. Noble, (AM +KS +58969 +BJR +796); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +11 Dec +, 2001, J. Noble, (AM +KS +76808 +BJR +802); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +11 Dec +, 2001, J. Noble, (AM +KS +76808 +BJR +802); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +9 Oct +, 1999, J. Noble, (AM +KS +62821 +BJR +803); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +10 Jan +, 2001, J. Noble, (AM +KS +76766 +BJR +804); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +6 Mar +, 2001, J. Noble, (AM +KS +72867 +BJR +805); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +20 Nov +, 2001, J. Noble, (AM +KS +76783 +BJR +806); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +4 Dec +, 2001, J. Noble, (AM +KS +72879 +BJR +807); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +15 Sep +, 2002, J. Noble, (AM +KS +79713 +BJR +810); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +4 Jan +, 2002, J. Noble, (AM +KS +76893 +BJR +811); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +1 Oct +, 2002, J. Noble, (AM +KS +76847 +BJR +814); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +5 Oct +, 2002, J. Noble, (AM +KS +79737 +BJR +819); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +4 Dec +, 2001, J. Noble, (AM +KS +72899 +BJR +820); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +25 Apr +, 2001, J. Noble, (AM +KS +72874 +BJR +821); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +7 Apr +, 2002, J. Noble, (AM +KS +79749 +BJR +822); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +1 Jun +, 2000, J. Noble, (AM +KS +65827 +BJR +823); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +8 Mar +, 2003, J. Noble, (AM +KS +87225 +BJR +824); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +21 Aug +, 2002, J. Noble, (AM +KS +84296 +BJR +825); 1 imm. Beecroft Reserve, +151.07°E +, +33.75°S +, +21 Aug +, 2002, J. Noble, (AM +KS +84303 +BJR +827); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +7 Apr +, 2002, J. Noble, (AM +KS +79750 +BJR +828); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +19 May +, 2002, J. Noble, (AM +KS +79744 +BJR +829); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +5 May +, 2002, J. Noble, (AM +KS +79726 +BJR +832); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +25 Jul +, 2001, J. Noble, (AM +KS +76822 +BJR +833); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +2 Apr +, 2000, J. Noble, (AM +KS +66015 +BJR +836); 1M, Beecroft Reserve, +151.07°E +, +33.75°S +, +5 May +, 2002, J. Noble, (AM +KS +79725 +BJR +838); 1F, Beecroft Reserve, +151.07°E +, °S, 33.75, +10 Mar +, 1999, J. Noble, (AM +KS +66213 +BJR +841); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +4 Jan +, 2002, J. Noble, (AM +KS +76890 +BJR +842); 1F, Beecroft Reserve, +151.07°E +, +33.75°S +, +15 Dec +, 2002, J. Noble, (AM +KS +84265 +BJR +843); 1F, Lindfield, +151.17°E +, +33.78°S +, +16 Oct +, 1966, D. Doolan, (AM +KS +18981 +BJR +569); 1F, Wallumatta Nature Reserve, North Ryde., +151.12°E +, +33.80°S +, +26 Nov +, 2002, (G. Milledge, (AM +KS +81953 +BJR +834); 1M, Lilyfield, +151.15°E +, +33.87°S +, +18 Nov +, 1956, A. Musgrave, (AM +KS +49873 +BJR +783); 1F, Sydney Royal National Park, +151.07°E +, +34.13°S +, +12 Feb +, 1981, Horseman & Harland, (AM +KS +8650 +BJR +574); 1F, Stony Range, +150.83°E +, +34.55°S +, +26 Sep +, 1997, D. Mead-Hunter, ( +WAM +T66947 +BJR +496); 1M, +Macquarie +Pass, +Macquarie +Pass NP, +150.65°E +, +34.57°S +, +9 Dec +, 1999, G. Milledge, (AM +KS +58745 +BJR +706); 1F, Jamberoo Mountain, +150.72°E +, +34.67°S +, +4 Nov +, 1994, J. Noble, (AM +KS +51656 +BJR +695); 1M, Jamberoo Mountain, +150.72°E +, +34.67°S +, +9 Nov +, 1997, J. Noble, (AM +KS +51451 +BJR +707); 1F, Jamberoo Mountain, +150.72°E +, +34.67°S +, +1 Feb +, 2000, J. Noble, (AM +KS +65678 +BJR +809); 1F, Jamberoo Mountain, +150.72°E +, +34.67°S +, +20 Apr +, 1995, J. Noble, (AM +KS +79779 +BJR +812); 1M, Barren Grounds Nature Reserve, +150.72°E +, +34.68°S +, +27 Oct +, 2002, M. Gray, (AM +KS +81939 +BJR +835); 1M, 1F,, Foxground, near Gerringong, +150.77°E +, +34.72°S +, +29 Oct +, 2002, M. +Zabka +, M. Gray, (AM +KS +81354 +BJR +818); 1M, Gerringong, +150.83°E +, +34.73°S +, +13 Mar +, 1997, G. Wishart, (AM +KS +50105A +BJR +753.1); 1M, Seven Mile Beach NP., +150.77°E +, +34.82°S +, +28 Oct +, 2002, M. Gray, (AM +KS +81905 +BJR +839); 1F, +2km +west of Narooma, +150.12°E +, +36.22°S +, +7 Nov +, 2007, B.J. Richardson, ( +ANIC +42 0 0 1193 +BJR +966). +AUSTRALIAN CAPITAL TERRITORY +: 1F, Canberra, +149.13°E +, +35.30°S +, 1960, E. McCallan, ( +ANIC +42 0 0 0 291 +BJR +428.1). + + + + +FIGURES 47–54. + +Servaea villosa + +. 47–48 dorsal view (47 female, 48 male); 49–50 female genitalia (49 dorsal view of cleared specimen, 50 ventral view of external characteristics); 51–53 male palp (51 ventral view, 52 anterior lateral view, 53 posterior lateral view); 54 known and predicted distribution. Scale: total body 1 mm; remainder 0.2 mm. + + + + +Diagnosis. +This is a small species (CL, < +3mm +), in which the fertilization ducts are short and the insemination ducts reach the anterior edge of the fossa. It is distinct from all other species in the genus as the origin of the embolus is near the proximal rather than distal edge of the bulb. A median black mark is found on the posterior edge of the abdomen unlike all other species. When visible there is a distinctively shaped pattern in the middle of the dorsal abdomen. + + + + +Description. Male: +Cephalothorax dark orange covered with pennate ginger-brown hairs over dorsal surface with pennate grey hairs on the posterior and lateral surfaces. Integument surrounding ALE, PME and PLE black with thick covering of grey hairs. Clypeus narrow with long sparse fringe of grey hairs. Chelicerae long and strongly geniculate, dark tan with sparse covering of long white hairs on the proximal and median areas. A toothlike protuberance, projecting forwards off a large mound on the anterior face of each chelicera, a cluster of three large promarginal teeth and a separate small tooth on a single base and one large straight fissident retromarginal tooth. Endites and labium tan grading to yellow, sternum tan. Abdomen without a central anterior cleft, yellow with dark brown mid line stripe and brown patterning that reach the margins. Pattern highly variable, constant features are the black mid line marking at the posterior end of the abdomen and the shape of the chevron (when present). Ventral abdomen same colour as dorsal surface of the abdomen on the sides with a black central section. Spinnerets yellow. L1 longer and a little more robust than L2, L3 and L4. Femora of L1 and L2 brown with dark brown anterior lateral and ventral patches covering over half the segment. L3 and L4 femora with three transverse dark stripes.L3 and L4 femora, and all patellae, tibias, tarsi and metatarsi yellow, without fringing. Patella plain, tibia with two transverse brown bands, metatarsus with a single transverse band and tarsus with two transverse bands. +Palp +( +Figs 51–53 +): brown, tibia with single slender apophysis. Tegulum relatively broad with anterior lateral lobe and a proximal lobe, origin of the embolus proximal, forming a tapering single anticlockwise spiral around the bulb. Dimensions: CL 2.7±0.10 (16) (1.98–3.22), EFL 1.16±0.04 (16) (0.93–1.36), CW 2.11±0.08 (16) (1.49– 2.54), AEW 1.90±0.06 (16) (1.42–2.17), AMEW 1.12±0.03 (16) (0.87–1.30), PEW 1.79±0.06. + + +Female: +Cephalothorax dark orange covered with pennate grey hairs, thicker on the posterior and lateral surfaces. Integument surrounding ALE, PME and PLE black with covering of grey hairs. Clypeus narrow with long sparse fringe of grey hairs. Chelicerae geniculate, dark tan with a sparse long white hairs on the front face, four promarginal teeth on a single base and a single, large, fissident, retromarginal tooth but no protuberance on the front face. Endites and labium mid brown grading to yellow. Sternum mid brown. Abdomen with a slight central anterior cleft, yellow with dark brown to black markings. Pattern highly variable, constant features are the black mid line marking at the posterior end of the abdomen and the shape of the chevron. Ventral abdomen same colours as dorsal surface of the abdomen on the sides with a black central section. Spinnerets yellow. Palps orange with darker transverse bands. L4>L3> L1>L2, all relatively slender. Legs yellow grading distally to mid brown, femur without three dark brown transverse bands, patella with a single transverse brown band, tibia with two transverse brown bands and metatarsus with two transverse bands and tarsus with a single transverse band. +Epigynum +: consisting of two large fossae and a darker sclerotised margin. A distinct brown patch varying in shape and position is sometimes found in the middle of each fossa. Guides and copulatory openings indistinct. Guide consistent in shape but varying in position with different parts emphasised in different specimens. Anterior edge of the insemination duct beyond or near the anterior edge of the epigynum. Posterior edge of the insemination duct in line with or anterior to the matching edge of the guide. Accessory gland in the distal third of the insemination duct. Insemination duct passes laterally across the anterior part of the fossa to the mid line and then move posteriorly until entering the spermatheca on the posterior mid line. Spermatheca pear-shaped and within the margin of the fossa towards the posterior edge. Right and left spermatheca touching, insemination ducts well separated. The fertilization duct is short, arising from a branch of varying length off the anterior edge of the spermatheca and curving dorsally in a tight circle. +Dimensions: +CL 2.77±0.04 (26) 2.35–3.10, EFL 1.22±0.02 (26) 1.02–1.36, CW 2.27±0.03 (26) 1.98– 2.54, AEW 1.98±0.02 (26) 1.86–2.11, AMEW 1.1±0.01 (26) 1.05–1.30, PEW 1.91±0.02 (26) 1.67–2.11. + + + + +Distribution and biology. +Only found to the east of the Great Dividing Range from southern NSW to central Queensland ( +Fig. 54 +), though predicted to be found in Victoria and South +Australia +. Found under bark in eucalypt forest and woodlands. Likely IUCN Red List Category LC. + + + + \ No newline at end of file diff --git a/data/38/61/A1/3861A11D1D315B408E9DCC612833EFA6.xml b/data/38/61/A1/3861A11D1D315B408E9DCC612833EFA6.xml new file mode 100644 index 00000000000..8efb1e580ee --- /dev/null +++ b/data/38/61/A1/3861A11D1D315B408E9DCC612833EFA6.xml @@ -0,0 +1,642 @@ + + + +Wandering throughout South America: Taxonomic revision of Tradescantia subg. Austrotradescantia (D. R. Hunt) M. Pell. (Commelinaceae) + + + +Author + +Pellegrini, Marco O. O. +https://orcid.org/0000-0002-8783-1362 +Universidade de Sao Paulo, Departamento de Botanica, Rua do Matao 277, CEP 05508 - 900, Sao Paulo, SP, Brazil +marcooctavio.pellegrini@gmail.com + +text + + +PhytoKeys + + +2018 + +2018-07-19 + + +104 + + +1 +97 + + + + +http://dx.doi.org/10.3897/phytokeys.104.28484 + +journal article +http://dx.doi.org/10.3897/phytokeys.104.28484 +1314-2003-104-1 +FF8ABC62FF83D2362B47F826FFDCFF8A +1322211 + + + + + +13 +. +Tradescantia umbraculifera Hand.-Mazz., Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 79: 204. 1908. +Figs 32 +, 33 + + + + +Tradescantia fluminensis var. pubescens +C.B.Clarke in De Candolle & De Candolle, Monogr. Phan. 3: 295. 1881. Lectotype (designated here). BRAZIL. Provincia de St. Paul and Rio, southern Brazil, fl., 1861-1862, J. Weir s.n. (K barcode K000363269!). +Syn. nov. + + + +Type material. + +Lectotype (designated by +Hassemer et al. 2017 +). BRAZIL. +Sao +Paulo: Campinas, fl., Jan 1900, J. Campos Novaes 1218 (WU barcode WU0061328!; isolectotype: US barcode US00046114!). + + + +Description. + +Herbs +ca. 30-80 cm tall, with an indefinite base, terrestrial, rupicolous or epiphytes. +Stems +prostrate with ascending apex, succulent to slightly fibrous, little to densely branched; internodes 2.8-10 cm long at base, distally shorter, light to medium to dark green or reddish-purple to vinaceous, glabrous to sparsely pilose, with a leaf-opposed longitudinal line of short, uniseriate, hyaline to light brown hairs in the terminal portion of the stems. +Leaves +distichously-alternate, sessile; ptyxis involute; sheaths 0.5-2.3 cm long, light to medium to dark green or reddish-purple to vinaceous, glabrous to pilose to sparsely hispid, margin densely setose, hairs hyaline to light brown; blades 3.8-19.1 +x +1-3.5 cm, linear lanceolate to lanceolate or narrowly lanceolate to lanceolate, flat, chartaceous, sometimes membranous, glabrous on both sides or adaxially glabrous and abaxially pilose, hairs hyaline to light brown, adaxially medium to dark green, abaxially light to medium green, rarely vinaceous, turning dark brown to black when dry, base truncate to amplexicaulous or round, margins green, ciliolate to ciliolate, flat, apex acuminate to caudate; midvein conspicuous, adaxially impressed, secondary veins conspicuous, adaxially slightly impressed to impressed, abaxially prominent, becoming more evident on both sides when dry. +Synflorescences +terminal or axillar in the distal portion of the stems, composed of a solitary main florescence, 1-4 per leaf axis. +Inflorescences (main florescences) +consisting of a pedunculate double-cincinni fused back to back; peduncles 0.5-4.3 cm long, light to medium to dark green, glabrous to pilose, with a dense longitudinal line of short, uniseriate, hyaline to light brown hairs; cincinni bracts 0.5-1.5(-2.3-6.2) +x +0.2-1(-1.4) cm, similar to each other, cordate to broadly cordate, rarely lanceolate, spathaceous, rarely leaf-like, glabrous or pilose to sparsely hispid, medium to dark green, abaxially light to medium green, base cordate to obtuse, saccate, margins ciliolate to ciliolate, flat, apex acute, rarely acuminate; double +cincinni +(4-)8-12-flowered. +Flowers +1.3-2.2 cm diam., pedicels 0.5-1.2 mm long, white to vinaceous, rarely green, glabrous to sparsely glandular-pubescent; floral buds ellipsoid; sepals 5.2-8.1 +x +2-3.7 mm, dorsally keeled, green, glabrous or pilose, with hairs generally along the keel and at the base of the sepals close to the pedicel, hyaline to light brown; petals 0.7-1.2 +x +0.3-0.6 cm, white; filaments 4.7-6.8 mm long, anthers 0.8-1 +x +0.9-1.2 mm; ovary 1.2-2 +x +0.8-1.3 mm, style 4.5-6.2 mm long; pistil longer than the stamens. +Capsules +2.5-3.8 +x +2.1-2.7 cm. +Seeds +1.6-1.9 +x +1.2-1.5 mm, testa grey to greyish-brown, not cleft towards the embryotega, costate; hilum longer than +1/2 +the length of the seed. + + + +Specimens see. + +ARGENTINA. Chaco +: 1° de Mayo, Colonia +Benitez +, fl., 10 Nov 1973, A.G. Schulz s.n. (CORD no. 469148, CTES no. 203094). +Corrientes +: +Ituzaingo +, Desembocadura del Arroyo +Garape +em el +Rio +Parana +, 45 km al E de +Ituzaingo +, fl., fr., 24 Apr 1975, A. Schinini et al. 11243 (CTES). +Misiones +: Apostoles, San Jose, fl., 11 Feb 1947, A.M.B. Huidobro 4981 (K, LIL); +Cainguas +, Salto Marvilla, fl., 4 May 1999, N.B. Deginani et al. 998 (CORD, CTES, SI); Candelaria, Cerro Azul, fl., fr., 16 Feb 1947, A.M.B. Huidobro 5282 (K, LIL); Loreto, fl., 12 May 1946, J.E. Montes 2223 (K, LIL); road from Bonpland to +Obera +, fl., 23 Feb 1984, T.M. Pedersen 13668 (L); Picada Guemes, fl., fr., 21 Feb 1947, A.M.B. Huidobro 4859 (K, LIL); Profundidad, fl., 19 Sep 1974, A. Krapovickas et al. 25711 (CTES); Candelaria-Loreto, fl., fr., 22 Jul 1949, J.E. Montes 4222 (LIL, LP); +Concepcion +de la Sierra, fl., 3 Feb 1948, A. Schinini 6979b (CORD, CTES); Eldorado, ruta 17, desvio 2 km a San Pedro, fl., 20 Jan 1973, A. Schinini & A. Fernandez 5933 (CORD, CTES); ruta 17, 89 km E de Eldorado, fl., 22 Jan 1973, A. Schinini & A. Fernandez 6002 (CORD, CTES); General Manuel Belgrano, 12 km S de Bernardo de Irigoyen, ruta 14, Cerro Tigre, fl., 15 Feb 1970, V. +Marunak +107 (CORD, CTES, LP); +Guarani +, Predio +Guarani +, picada al Arroyo Soberbio, fl., 15 Mar 1994, S. Tressens et al. 4881 (CORD, CTES); rumbo cerca de Papael Misionero, fl., 28 Apr 1999, S. Tressens et al. 6279 (CTES, K); +Iguazu +, Rio +Parana +, 10 km S de Puerto +Iguazu +, frente a Puerto Bertoni, fl., 28 Mar 1970, A. Krapovickas et al. 15780 (CORD, CTES); Parque Nacional +Iguazu +, Sendero Macuco, fl., 6 Aug 1991, R. Vanni et al. 2666 (CORD, CTES); fl., 23 Apr 1996, J. Herrera 174 (CTES); Leandro M. Alem, 2 km al NE de Cerro Azul, fl., 10 Mar 1969, A. Krapovickas et al. 15070 (CORD, CTES); Libertador General San +Martin +, Predio UNLP, valle del arroyo +Cuna +Piru +, fl., fr., 19 Jul 1998, F. Biganzoli et al. 126 (LP, SI); Montecarlo, Arroyo Piray +Guazu +y ruta 12, fl., 15 Feb 1980, A. Schinini 19909 (CTES); San Ignacio, fl., 3 Feb 1947, J.E. Montes 822 (BA, LIL); Posadas, +Jardin +Botanico +, fl., 17 Jul 2001, M. Grabiele 5 (CORD, CTES, MNES); San Pedro, 89 km E de Eldorado, fl., 22 Jan 1973, A. Schinini & A. Fernandez 6014 (CORD, CTES); ruta provincial 17, +desvio +5 km a Tobuna por ruta provincial 224, fl., 26 Jan 1973, A. Schinini & A. Fernandez 6100 (CORD, CTES); entre San Pedro y Puerto Piray, 20 km de San Pedro, ruta provincial 16, fl., 28 Feb 1995, F.O. Zuloaga et al. 5063 (CORD, CTES, SI); cruzando el Puente sobre el +Yaboti +hacia los obrajes, ruta proyectada 102, fl., 9 May 1999, N.B. Deginani et al. 1213 (CORD, CTES, SI); Santa Anna, fl., 1907, s.leg. s.n. (LP no. 19175). +BRAZIL. Minas Gerais +: s.loc., fl., fr., 1816-1821, A. Saint-Hilaire D 548 (P); Aiuruoca, PCH-Aiuruoca, +area +de +vazao +reduzida, RPPN Cachoeira do Tombo, fl., 26 +Mar +2009, P.H.A. Melo & D.M. Torres 3392 (ESAL, RB); Caldas, fl., 23 Mar 1868, A.F. Regnell 1445 (US); Cambuquira, Fazenda Esplanada, fl., fr., 25 Mar 2004, M.C. Weyland Vieira 2025 (RB); Carrancas, Serra de Bicas, fl., 30 Apr 1999, A.O. +Simoes +et al. 821 (UEC); Lima Duarte, Parque Estadual da Serra do Ibitipoca, trilha entre a Gruta do Fugitivo e Gruta dos +Tres +Arcos, fl., 11 Mar 2004, R.C. Forzza et al. 3173 (CEPEC, K, MBM, NY, RB, SPF, UEC); entre a Gruta dos Viajantes e a Gruta dos +Tres +Arcos, fl., 20 Jan 2005, R.C. Forzza et al. 3965 (K, MBM, RB, SPF, UEC); Gruta dos +Tres +Arcos, fl., 17 Mar 2005, R. Dias-Melo et al. 234 (CEPEC, NY, RB); Gruta dos Viajantes, +corrego +Monjolinho, fl., 25 Jan 2010, R. Mello-Silva 3239 (RB, SPF); +Sao +Thome +das Letras, +proximo +ao Pico do +Gaviao +, fl., 22 Feb 1999, M.C. Assis et al. 596 (RB, SPF); APA +Sao +Thome +, Vale do Can +tagalo +, fl., 4 Feb 2015, E.R. Sattelmayer 22 (HUSC, RB). + +Parana + +: +Adrianopolis +, Ponte do Ribeira, fl., fr., 20 Feb 1981, G. Hatschbach & A. +Martinez +43629 (CORD, MBM, US); Rio Itapeva, fl., 19 Feb 1981, G. Hatschbach & A. +Martinez +43622b (CORD, MBM, US); Antonina, Rio Cotia, fl., 24 Mar 1966, G. Hatschbach 14155 (MBM, P, RFA, US); Arapongas, Fazenda Solana, fl., 19 Feb 2009, M. Ferreira Jr. & E.M. Francisco 3 (FUEL); +praca +da igreja matriz, fl., 18 Jun 1988, L.V. Koga 10 (FUEL, HURB); Cerro Azul, cabeceira do Rio do Tigre, fl., 18 Jul 1984, G. Hatschbach 48100 (MBM, US); fl., 24 Apr 1987, G. Hatschbach et al. 51236 (MBM, US); +Cornelio +Procopio +, Parque Estadual Mata +Sao +Francisco, fl., fr., 13 Mar 2009, G.M. Ferreira 358 (FUEL, UNIFIL); Foz do +Iguacu +, Parque Nacional do +Iguacu +, fl., 25 Apr 1949, J. +Falcao +96 (RB); fl., 19 Feb 1960, E. Pereira 5364 (HB, RB); Londrina, +Pirapo +, fl., s.dat., G. Tessmann 1938 (FUEL, US); Londrina, estrada Paiquere, +proximo +a +Fazenda Figueira, fl., 7 Feb 2003, D.A. Estevan et al. 1259 (FUEL); Fazenda Santa Helena, fl., fr., 5 Mar 2009, E.M. Francisco 2020 (FUEL); Parque Estadual Mata dos Godoy, fl., fr., 8 Mar 2010, E.F.S. Rossetto & E.M. Francisco 52 (FUEL); +Maua +da Serra, +Estancia +Manain, fl., fr., 1 Apr 2008, V.M. Cotarelli & E.M. Francisco 70 (FUEL); Rio +Tres +Bocas, fl., fr., s.dat., R. Hertel s.n. (MBM no. 181892, US barcode US00046118); Rio Branco do Sul, Serra do Caete, fl., 10 Jan 1978, G. Hatschbach 40703 (MBM, US); fl., fr., 18 Feb 1981, G. Hatschbach & A. +Martinez +43603 (CORD, MBM, US); Santo +Antonio +da Platina, Morro da Telepar, fl., 30 Jan 1974, R. Kummrow 516 (K, MBM); Sapopema, fl., 5 Apr 1996, L.P. +Felix +& A. Leforge 11 (RB, UEC); +Telemaco +Borba, Fazenda Monte Alegre, estrada para a foz, fl., 20 Apr 2005, T.I.N. Azevedo et al. 81 (FUEL); estrada para a Ilha Surubim, fl., 20 Nov 1989, J.A. Pimenta et al. s.n. (FUEL no. 7628); +a +beira do +Ribeirao +Varanal, fl., 20 Apr 2005, T.I.N. Azevedo et al. 86 (FUEL); fl., 30 May 2006, T.I.N. Azevedo & S.I. Azevedo 324 (FUEL). +Rio de Janeiro +: Itatiaia, +Macico +do Itatiaia, Parque Nacional do Itatiaia, estrada para o Pico das Agulhas Negras, fl., 15 Feb 1995, J.M.A. Braga et al. 2015 (RB); estrada +regiao +do planalto, fl., fr., 31 Jan 1966, S.V. Andrade 730 (RB); fl., 23 Jan 2012, M.O.O. Pellegrini 192 (RB); fr., 10 Jun 2012, M.L.O. +Trovo +et al. 569 (RB); fl., 2 Feb 2014, L.S.B. Calazans et al. 241 (RB); fl., 7 Feb 2015, R.G. Barbosa-Silva et al. 421 (RB); Agulhas Negras, fl., 17 Apr 1971, I.S. Gottsberger & G.K. Gottsberger 122-17471 (UB, US); Resende, Parque Nacional do Itatiaia, BR-485, Brejo da Lapa, fl., fr., 22 Feb 2014, L.S.B. Calazans et al. 241 (HRCB, RB, VIES); Rio de Janeiro, Realengo, fl., s.dat., C.V. Freire 397 (R); +Teresopolis +, Parque Nacional da Serra dos +Orgaos +, fl., fr., 16-17 Oct 1958, R. Schnell 8256 (BR, P); fl., 10 Jul 1966, A. Lourteig 1854 (K, P, R); fl., 3 Aug 1966, D.R. Hunt 6482 (K, US); fl., 5 Jul 1970, J. Barcia 82 (R); trilha para a Pedra do Sino, fl., 05 Dec 2001, F. Feres et al. 19 (RB, UEC); fl., fr., 12 Sep 2014, L.S.B. Calazans et al. 453 (RB); trilha do Rio Soberbo, fl., 22 Aug 2010, M. Nadruz et al. 2471 (RB). +Rio Grande do Sul +: Derrubadas, Tenente Portela, Parque Estadual do Turvo, Salto +Yucuna +, fl., 17 Mar 1977, K. Hagelund 11236 (CORD); fl., Mar 1980, J. Mattos et al. 21283 (HAS); fl., 1980, J.E.A. Mariath s.n. (CORD no. 467395, ICN no. 50979); +Maquine +, Reserva +Biologica +da Serra Geral, Vale Linha Encantada, fl., Nov 2003, M.L. Abruzzi 5151 (HAS); +Sao +Leopoldo, Morro Sapucaia, fl., 5 Aug 1949, B. Rambo 42798 (HBR); fl., fr., 11 Oct 1955, B. Rambo 57048 (HBR). +Santa Catarina +: Blumenau, Morro do Sapo, Parque Nacional Serra do +Itajai +, fl., +05 +Nov 2012, L.A. Funez 1285 (FURB, HAVAT); Morro do Cachorro, fl., 31 Jan 2014, A.L. Gasper et al. 3439 (FUEL, FURB); Dona Emma, Gruta Nossa Senhora de +Fatima +, fl., 26 Jan 2012, L.A. Funez 309 (FURB); RPPN Bugerkopf, trilha principal, fl., fr., 6 Feb 2013, L.A. Funez 1681 (FURB); +Florianopolis +, trilha na margem sul da lagoa, Lagoa do Peri, fl., 3 Mar 2016, F.A. Silva Filho 963 (FLOR, RB); Ibirama, fl., 20 Oct 1953, R.M. Klein 614 (HBR, US); fl., 20 Sep 1956, R. Reitz & R.M. Klein 3692 (HBR, K, MBM, NY, UPCB); +Itaiopolis +, Arroio das Pombas, fl., 3 Feb 2010, A. Korte & A. Kniess 1631 (FURB); Itapiranga, Laranjeiras, SC-66, fl., 14 Feb 2009, M. Verdi et al. 1631 (FURB); +Jaragua +do Sul, Serra do +Jaragua +, fl., 31 Aug 1997, P. Schwacke 13350 (RB); Luiz Alves, +Braco +Joaquim, fl., 22 Mar 1956, R. Reitz & R.M. Klein 2886 (HBR, US); +Mondai +, fl., 4 Feb 2009, M. Verdi et al. 2638 (FURB, RB); Linha Cascalho, fl., 5 Mar 2009, M. Verdi et al. 1746 (FURB, RB); Linha Capirara, BR-283, fl., 9 Mar 2009, M. Verdi et al. 77 (FURB, LUSC); Nova +Teutonia +, fl., 8 Apr 1944, F. Plaumann 444 (RB); Palmitos, 24 km E of Mondai, fl., 25 Feb 1957, L.B. Smith & R. Klein 11828 (HBR, NY, US); +Paraiso +, Rio das Flores, fl., 1 Mar 1964, A. Castellanos 24799 (CORD, K, RB); +Sao +Miguel +D'Oeste +, Peperi, fl., fr., 1 Mar 1964, R.M. Klein 5107 (HBR); +Romelandia +, +Esperanca +, fl., 2 Mar 2009, A. Stival-Santos & S. Silveira 439 (FURB, RB); +Sao +Bento do Sul, Ano Bom/ +Braco +Esquerdo, fl., 29 Jan 2010, S. Dreveck & F.E. Carneiro 1667 (FURB); +Timbo +, Castelo dos Padres, fl., 2 Oct 2014, M.O.O. Pellegrini et al. 429 (RB); Vidal Ramos, +Sabia +, fl., 14 Jun 1957, R. Reitz & R.M. Klein 4284 (HBR, US); fl., 26 Nov 1957, R.M. Klein 2233 (HBR, NY, US). + +Sao +Paulo + +: s.loc., fl., 1816-1821, A. Saint-Hilaire D 632 (P); Atibaia, Pedra Grande, fl., 29 Jan 1986, N. Taroda & K. Yamamoto 18324 (UEC); Barra do Turvo, 10 km de Barra do Turvo em +direcao +a +Pariquera-acu +, fl., fr., 14 Feb 1995, J.P. Souza et al. 89 (ESA, SP, UEC, UFP); +Cananeia +, Parque Estadual da Jacupiranga, fl., fr., 24 Mar 2005, M. Carboni et al. 119 (ESA, UEC); +Iepe +, Fazenda C.A.P.I., about 5 km E of Porto Alvorada, along the rio Paranapanema, fl., 9 Feb 1965, G. Eiten et al. 5998 (EAC, INPA, MO, NY, SP, UB, US); Ilhabela, Parque Estadual da Ilhabela, trilha da +Agua +Branca, fl., 23 Aug 1995, A. Rapini 48 (SP, SPF, UEC, UFP); +Sao +Paulo, Eldorado Paulista, Parque Estadual Jacupiranga, +Nucleo +Cedro, fl., fr., 14 Feb 1995, H.F. +Leitao +Filho et al. 33267 (HRCB, SP, SPF, UEC); Jardim +Botanico +e Parque do estado, fl., fr., 10 Aug 1967, R. Faria 40 (SP); Serra da Cantareira, fl., 13 Apr 1901, s.leg. 300 (SP); Serra da Cantareira, no Horto Florestal, fl., 30 Mar 1967, J. Mattos 14542 (HAS, K, RB, SP). +PARAGUAY. Without province +: s.loc., fl., s.dat., Fleischer s.n. (P barcode P02174039). + +Alto +Parana + +: s.loc., fl., 1909-1910, K. Fiebrig 6236 (K, L, US); Ciudaded del Este, Puerto Presidente Stroessner, fl., May 1983, L.C. Stutz 1773 (CORD, U, US); Puerto Embalse, fl., Mar 1942, L. +Jimenez +122 (SCP); fl., Mar 1942, C.V. Pavetti Morin 488 (SCP); Vivero Florestal +Itaipu +, fl., 13 Jul 1980, G. Caballero Marmori 739 (CORD, CTES). + +Canindeyu + +: Jejui-mi, a unos 1500 m al N de la caseta, fl., 8 May 1996, G. +Marin +& B. +Jimenez +191 (BM, CORD, CTES, FMB, PY). + +Guaira + +: Colonel Independencia, propriedad Vurtz, fl., 6 Oct 1967, A. Lourteig 1931 (P, US); Arroyo +Guazu +, camino a San Gervasio, fl., 27 Mar 1993, A. Schinini et al. 28031 (CORD, CTES); Reserva +Ybytyruzu +, fl., 27 Feb 2011, M. Vera et al. 2741 (FCQ); Tebicuary, Azucarera Paraguaya, fl., Jul 1942, C.V. Pavetti Morin 1186 (SCP); Villarica, Santa Barbara, fl., 26 Feb 1876, B. Balansa 590 (K, P). + +Paraguari + +: Ybycui Na +tional +Park, fl., 24 Jan 1989, E.M. Zardini & A. Aguayo 10090 (K, LP, MO, PY); fl., 15 May 1989, A. Aguayo 183 (CORD, US). + + + +Distribution and habitat. + +Argentina and Brazil (states of Minas Gerais, Rio de Janeiro, +Sao +Paulo, +Parana +, Santa Catarina and Rio Grande do Sul) and Paraguay; in the Atlantic Forest, Cerrado and Chaco domains (Fig. +33 +). It can be found growing as terrestrial and epiphyte understorey in shaded and moist forests. + + + +Phenology. +It was found in bloom and fruit throughout the year but peaking between August and February. + + +Etymology. + +The epithet " +umbraculifera +" means "carrying several umbrellas", making reference to the many inflorescences per leaf axil this species generally produces and, most importantly, to the its small spathaceous cincinni bract. + + + +Conservation status. + + +Tradescantia umbraculifera + +possesses a wide EOO (ca. 764,678.067 km2), forming dense subpopulations in shady and moist understorey. Thus, in accordance with the IUCN recommendations ( +IUCN 2001 +), it should be considered Least Concern (LC). + + + +Comments. + + +Tradescantia umbraculifera + +is a member of the + +T. fluminensis + +group ( +Pellegrini 2017 +), due to its indefinite base, prostrate stems (Fig. +32A +), involute ptyxis, leaf-blades with impressed secondary veins (Fig. +32C +), saccate cincinni bracts (Fig. +32E-G +) and seeds not cleft towards the embryotega (Fig. +32K +). Furthermore, dried specimens of + +T. umbraculifera + +acquire a peculiar dark brown to black colouration, which is recorded in +T. subg. Austrotradescantia +for + +T. chrysophylla + +, + +T. cymbispatha + +and some specimens of + +T. fluminensis + +. Nonetheless, it is one of the most peculiar species in +T. subg. Austrotradescantia +, due to its generally acuminate to caudate leaf-blades (Fig. +32C +), numerous inflorescences per leaf axis (Fig. +32E, F +), spathaceous cincinni bracts (Fig. +32E-G +), white to vinaceous pedicels (Fig. +32H +), pistil longer than the stamens (Fig. +32G +) and hilum longer than +1/2 +the length of the seed (Fig. +32K +). This combination of characters differentiates + +T. umbraculifera + +from all remaining species of +T. subg. Austrotradescantia +. Smaller specimens of + +T. umbraculifera + +can be more easily confused with + +T. fluminensis + +but can be easily differentiated based on inflorescence and seed characters. Despite the distinction between + +T. umbraculifera + +and + +T. fluminensis + +being generally clean-cut, some specimens were especially challenging to certainly identify. This is mainly due to the presence of leaf-like, instead of spathaceous cincinni bracts (easily observable in herbarium specimens) and intermediate floral features between the two species (observable only in fresh specimens; Fig. +32J +), such as: the colour of the pedicels, shape of the petals, length and density of the filaments hairs and pistil length. These specimens are hypothesised to represent naturally occurring hybrids between both species, since they were observed in areas where both + +T. umbraculifera + +and + +T. fluminensis + +were known to occur. However, due to the lack of reproductive, hybridisation and cytological studies, I have chosen to tentatively recognise these specimens under a broader sense of + +T. umbraculifera + +. Further studies might confirm my assumptions of the natural occurrence of hybrids between + +T. umbraculifera + +and + +T. fluminensis + +. Despite the small morphological resemblance, herbarium specimens of + +T. umbraculifera + +have been previously confused in Southern Brazil with + +T. tenella + +. Both species share only a handful of morphological characters, all of them being synapomorphies of the + + +T +. fluminensis + + +group. + +Tradescantia umbraculifera + +can be easily differentiated from + +T. tenella + +due to its robust habit ( +vs. +generally small in + +T. tenella + +), indefinite base ( +vs. +definite), prostrate stems ( +vs. +erect), sessile leaves ( +vs. +subpetiolate), 1-4 main florescences per leaf axil ( +vs. +always 1), cincinni bracts spathaceous and equal ( +vs. +leaf-like and unequal) flowers 1.3-2.2 cm diam. ( +vs. +0.4-1 cm diam.), petals always white ( +vs. +ranging from white to pink), pistil longer than the stamens ( +vs. +equal), seeds with costate testa ( +vs. +rugose) and hilum longer than +1/2 +the length of the seed ( +vs. +shorter than +1/2 +the length of the seed). + + +Despite being in different morphological groups, herbarium specimens of + +T. umbraculifera + +have also been confused with + +T. crassula + +. This might be due these species robust habit, sessile leaves, sepals with hairs restricted to the dorsal keels, petals always white, pistil longer than the stamens and hilum longer than +1/2 +the length of the seed. Nonetheless, + +T. umbraculifera + +can be easily differentiated by its indefinite base ( +vs. +definite in + +T. crassula + +), prostrate stems ( +vs. +erect), 1-4 main florescences per leaf axil ( +vs. +always 1), cincinni bracts spathaceous and saccate ( +vs. +leaf-like and non-saccate) and seeds not cleft towards the embryotega ( +vs. +cleft). + + + +Figure 32. + +Tradescantia umbraculifera + +Hand.-Mazz. +A +habit (replaced) +B +detail of the stem and the leaf-sheath, showing the leaf-opposed line of uniseriate hairs and the setose leaf-sheath margin +C +adaxial side of the leaf-blade, showing the impressed secondary veins +D +abaxial side of the leaf-blade +E +synflorescence +F +detail of the synflorescence, showing two inflorescences emerging from the same leaf axil and the spathaceous and saccate cincinni bracts +G +detail of the inflorescence, showing the spathaceous and saccate cincinni bracts and the side view of a flower, showing the pistil longer than the stamens +H +flower at post-anthesis showing the white pedicel and the glabrous sepals +I-J +flowers +I +front view of a flower of a typical specimen of + +T. umbraculifera + +J +front view of a flower of a putative hybrid between + +T. umbraculifera + +and + +T. fluminensis + +, showing the leaf-like cincinni bracts, ovate petals, sparser filament hairs +K +dorsal and ventral views of the seed, showing the costate testa not cleft towards the embryotega and the hilum longer than +1/2 +the length of the seed. Photos by M.O.O. Pellegrini, except +E, G-H, I +by H. Medeiros. See the Erratum note. + + + + +Figure 33. +Distribution of + +Tradescantia umbraculifera + +Hand.-Mazz. Orange- Cerrado; Yellow- Chaco and Pantanal; Olive-green- Pampa; Dark green- Atlantic Forest. + + + + + + \ No newline at end of file diff --git a/data/38/61/AB/3861AB258C6D5C6067BCF8902B2D21E8.xml b/data/38/61/AB/3861AB258C6D5C6067BCF8902B2D21E8.xml new file mode 100644 index 00000000000..90c6b096035 --- /dev/null +++ b/data/38/61/AB/3861AB258C6D5C6067BCF8902B2D21E8.xml @@ -0,0 +1,179 @@ + + + +The genus Pterostichus in China II: the subgenus Circinatus Sciaky, a species revision and phylogeny (Carabidae, Pterostichini) + + + +Author + +Shi, Hongliang + + + +Author + +Liang, Hongbin + +text + + +ZooKeys + + +2015 + +536 + + +1 +92 + + + + +http://dx.doi.org/10.3897/zookeys.536.5982 + +journal article +http://dx.doi.org/10.3897/zookeys.536.5982 +1313-2970-536-1 +A8B92CDD0B8C4384AAC559648BB45AA5 + + + +Taxon classification Animalia Coleoptera Carabidae + + + +Pterostichus (Circinatus) beneshi Sciaky, 1996 +Figures 24, 50, 51, 68, 87, 109 + + + + +Pterostichus (Circinatus) beneshi +Sciaky 1996 +: 225 (Original: +Pterostichus +( +Circinatus +); holotype deposited in CRS); +Bousquet 2003 +: 488; +Lorenz 2005 +: 280; +Allegro and Sciaky 2010 +: 4. + + + +Type locality. + +Sichuan: Wolong (ca. +N31.03° +, +E103.18° +), Wenchuan County, Sichuan province. + + + +Type material examined. + +Holotype of +Pterostichus beneshi +Sciaky (CRS), male, body length = 11.2 mm, board mounted, genitalia dissected and glued on same board with specimen, "Cina - W Sichuan / Wolong / 150 Km NW Chengdo / 9. VII. 94. +Benes." +; "HOLOTYPUS / Pterostichus / (Circinatus)/ beneshi sp. n. / Det. Sciaky, 1994" [red label]. + + + +Non-type material examined + +(total 53 specimens). 3 males, 7 females (IZAS), "Sichuan, Wolong, Wulidun, pit fall trap, YU Xiaodong lgt.", various altitude between 2290m-2615m, and date between 2004 VI.6-VIII.8; 4 males, 1 female (IZAS), "Sichuan, Wolong, Wuyipeng, pit fall trap, YU Xiaodong lgt.", various altitude between 2545m-2630m, and date between 2004 VI.14-VIII.14; 8 males, 2 females (IZAS), "Sichuan, Wolong, Wuyipeng, Caoyuandi, pit fall trap, YU Xiaodong lgt.", various altitude between 2370m-2570m, and date between 2004 V.31-VIII.31; 1 male (IZAS), "Sichuan, Wolong, Wuyipeng, 1990.VII.20, T. Deuve et Xie Weiping"; 2 males (IZAS), "China, Sichuan, Baoxing county, Donglashan gorge park, +N30.41675 +, +E102.59366 +; 2012.VI.28D 1933m, Liu Ye, Shi Hongliang leg."; 3 males (IZAS), "China, Sichuan, Baoxing county, Jiajinshan mt., Mahuanggou, mixed forest, +N30.85669 +, +E102.76615 +, 2012.VI.29 D 2681m, Liu Ye, Shi Hongliang leg."; 1 male (IZAS), "China, Sichuan, Baoxing county, Jiajinshan mt., Borigou viewing platform, mixed forest, +N30.82233 +, +E102.71886 +; 3238m, 2012.VI.29, Shi Hongliang, Liu Ye leg"; 1 male (IZAS), "Sichuan, Baoxing, Fengtongzhai, 1995m, 2001.VI.30-VII.3, YU Xiaodong lgt."; 1 female (IZAS), "Sichuan, Baoxing, Jiajinshan, Mahuanggou, 2495m, 2001.VII.2-5, YU Xiaodong, ZHOU Hongzhang lgt."; 4 males, 1 female (IZAS), "China, Sichuan, Tianquan, Erlangshan, 2500m, 2011.8.5, Huang Hao lgt."; 1 male, 2 females (IZAS), "China, Sichuan, Tianquan, Erlangshan, 2500m, 2011.7.21, Huang Hao lgt."; 5 males, 2 females (IZAS), "China, Sichuan Tianquan county, Erlangshan pass, meadow with shrubs, +N29.86240 +, +E102.28123 +; 2012.VI.20 D, pit fall trap, 2985, Liu Ye, Shi Hongliang leg."; 2 males (IZAS), "China, Sichuan, Tianquan county, Erlangshan pass, meadow with shrubs, 2985m, +N29.86240 +, +E102.28123 +, 2012.VI.24, pit fall trap, Shi Hongliang, LIU Ye lgt."; 2 males (IZAS), "Sichuan, Tianquan, Lianglu, Erlangshan, 2229m, 2014.IV.8, Yang Xiaodong lgt.". + + + +Diagnosis. +Pronotum with single mid-lateral seta; posterior seta distant from hind angle, hind angle completely rounded; basal foveal outer groove absent, outer region of inner groove completely flat; basal fovea area finely punctate between two inner grooves; elytral humeral tooth almost invisible; elytron with faint linear microsculpture; fifth tarsomeres glabrous beneath; terminal sternum of male not modified. + +This species is very similar to +Pterostichus zoiai +. They can be easily separated by their allopatric distribution. But morphologically, these two species can be separated only with difficulty by: (1) +Pterostichus beneshi +with apical lamella longer, length approx 3/4 of the basal width; +Pterostichus zoiai +with apical lamella shorter, length approx half the basal width; (2) +Pterostichus zoiai +with pronotum relatively narrower as indicated by +Allegro and Sciaky (2010 +: 18, key). These two species are very different in endophallus: +Pterostichus zoiai +with endophallus strongly bent dorsal-basally, the dorsal margin of endophallus closely adjacent to the apical orifice of aedeagus; dl and ll completely fused together. In +Pterostichus beneshi +, the endophallus fully expanded on the dorsal face of the aedeagus, the dorsal margin of the endophallus distinctly separate from the apical orifice; dl and ll well separated. (Figs 49, 50, 51) + + + +Supplemental description. +Male sternum. Penultimate and terminal sterna without special structures. Endophallus (Fig. 50D, E, G) extended in dorsal direction of aedeagus, main portion of endophallus located on dorsal side of aedeagus; gonopore (gp) located at level near middle of aedeagus, pointing to right (gonopore lobe folded in Fig. 50). Six distinct lobes recognized: dorsal lobe (dl) large with rounded apex, bent backward, close to apical orifice of aedeagus, dorsal half decorated with heavy scales; left lobe (ll) a little larger than dl, with finer scales, also bent backward; ventral lobe I (vl-I) small, tubiform, pointing in apical direction of aedeagus; ventral lobe II (vl-II) small, tubiform, a little longer than vl-I, apex slightly bent to right in dorsal view; right lobe (rl) shorter and thicker than vl-II; pre-apical lobe (pa) located on right surface, close to gp, apex enlarged, with very fine scales; basal-dorsal region on endophallus decorated with fine and dense scales; endophallus without chitinized piece. Female genitalia. Spermatheca with seminal canal approx 3.5 times as long as receptaculum; receptaculum capitate (Fig. 68), club approx half length of receptaculum; seminal canal inserted at base of common oviduct, base of seminal canal with sclerotized region long and thick. Stylomere II with two ensiform setae at basal half of outer margin, and a small one near middle of inner margin; two short nematiform setae located in a furrow near apex. Female sternum VIII (Fig. 87B) with fine setae on posterior margin, setae on middle region thicker; posterior margin narrowly notched in middle; posterior region well chitinized; anterior region weakly chitinized, deeply notched in middle; middle transparent region V-shaped, adjacent to anterior and posterior notches in middle. Female tergum VIII (Fig. 87A) short, posterior region semi-chitinized, with sparse and irregular spots; middle of anterior region with a chitinized large patch; anterior margin notched in middle, posterior margin evenly arcuate. + + +Distribution. + +Recorded from four counties of central Sichuan province: Wenchuan (Wolong nature reserve), Dayi (Xilingxueshan), Baoxing (south slope of Jiajinshan), and Tianquan (east slope of Erlangshan). In Wolong and Dayi, this species is sympatric with +Pterostichus xilingensis +, while it is sympatric with +Pterostichus pohnerti +in Baoxing and Tianquan (Maps 2, 3). + + + +Affinities. + +This species is very close to +Pterostichus zoiai +in their similarities of external appearance and male genitalia. The endophalli are also similar, and all lobes can be recognized as homologous. + + + +Geographical variation. + +We studied males from three localities: Wolong ( +N31.03° +, +E103.18° +), Erlangshan ( +N29.88° +, +E102.30° +), and Baoxing ( +N30.86° +, +E102.77° +). We found that the Erlangshan population is slightly different from the other two in male genitalia: (1) in the Erlangshan population, the apical lamella is slightly shorter and wider than that in the other two populations and is more similar to that in +Pterostichus zoiai +; (2) in the Erlangshan population, the endophallus with ll is strongly and abruptly narrowed to the apex, the upper margin is strongly sinuate, and the apex of ll is much narrower than that in the other two localities; and (3) in the Erlangshan population, vl-I and vl-II are much thicker than those in the other two localities (Figs 50, 51). + + + + \ No newline at end of file diff --git a/data/38/61/B6/3861B649A0FFF690A3CED49E93989E8C.xml b/data/38/61/B6/3861B649A0FFF690A3CED49E93989E8C.xml new file mode 100644 index 00000000000..2d92db9fa95 --- /dev/null +++ b/data/38/61/B6/3861B649A0FFF690A3CED49E93989E8C.xml @@ -0,0 +1,83 @@ + + + +A new species of Tegenaria Latreille, 1804 (Araneae, Agelenidae) from Turkey + + + +Author + +Kaya, Rahsen S. + + + +Author + +Kunt, Kadir B. + + + +Author + +Marusik, Yuri M. + + + +Author + +Ugurtas, Ismail H. + +text + + +ZooKeys + + +2010 + +51 + + +1 +16 + + + + +http://dx.doi.org/10.3897/zookeys.51.467 + +journal article +http://dx.doi.org/10.3897/zookeys.51.467 +1313-2970-51-1 + + + + +13. +Tegenaria hamid Brignoli, 1978 +Fig. 20 + + + + +Tegenaria hamid +Brignoli 1978b +: 515, fig. 96 (known from female only). + + + +General distribution: +Turkey. + + +Distribution in Turkey: + +Isparta Province: +Egirdir +District ( +Brignoli 1978b +). + + + + \ No newline at end of file diff --git a/data/38/61/F7/3861F7355D6507F59B05A53DEEA8B5B4.xml b/data/38/61/F7/3861F7355D6507F59B05A53DEEA8B5B4.xml new file mode 100644 index 00000000000..bb14ca6b30d --- /dev/null +++ b/data/38/61/F7/3861F7355D6507F59B05A53DEEA8B5B4.xml @@ -0,0 +1,75 @@ + + + +Four new species of Trigonopterus Fauvel from the island of New Britain (Coleoptera, Curculionidae) + + + +Author + +Van Dam, Matthew H. + + + +Author + +Laufa, Raymond + + + +Author + +Riedel, Alexander + +text + + +ZooKeys + + +2016 + +582 + + +129 +141 + + + + +http://dx.doi.org/10.3897/zookeys.582.7709 + +journal article +http://dx.doi.org/10.3897/zookeys.582.7709 +1313-2970-582-129 +3C1E0FB4634348949C34408983587BB7 + + + +Taxon classification Animalia Coleoptera Curculionidae + + + +Trigonopterus Fauvel, 1862 + + + +Type species. + +Trigonopterus insignis +Fauvel, 1862, by monotypy. + + + +Diagnosis. + +Fully apterous genus of +Cryptorhynchinae +. Length 1.5-6.0 mm. Rostrum in repose not reaching middle of mesocoxal length. Scutellar shield completely covered by elytra. Mesothoracic receptacle deep, posteriorly closed. Metanepisternum completely absent. Metathoracic spiracles located externally on side of metaventrite. Elytra with 9 striae (sometimes superficially effaced). Tarsal claws minute. Body usually largely unclothed. For additional information, see +van de Kamp et al. (2015) +and http://species-id.net/wiki/Trigonopterus. + + + + \ No newline at end of file diff --git a/data/38/61/FB/3861FBD8483747867DC29B8D83ED17E8.xml b/data/38/61/FB/3861FBD8483747867DC29B8D83ED17E8.xml new file mode 100644 index 00000000000..1997d3404a3 --- /dev/null +++ b/data/38/61/FB/3861FBD8483747867DC29B8D83ED17E8.xml @@ -0,0 +1,61 @@ + + + +Species plantarum: exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas + + + +Author + +Linnaeus, Carolus + +text + +1753 +Laurentius Salvius + +Stockholm + + + +https://doi.org/10.5962/bhl.title.669 + +book +10.5281/zenodo.3931989 +3931989 + + + + +Diosma uniflora +, +spec. nov. + + + +7. Diosma foliis ovato-oblongis, floribus solitariis terminalibus. + +Cistus humilis aethiopicus, inferioribus foliis rosmarini sylvestris punctatis, caeteris autem serpilli subrotundis, flore carneo. +Pluk. mant. 49. t.342. f.5. + + + + + +Habitat +in + +AEthiopia +. ♄ + + + + +Folia +rigidiora, & longe majora, quam in praecedentibus. +Flos +etjam sextuplo major: margine ut & subtus punctatus. + + + + \ No newline at end of file diff --git a/data/38/62/A5/3862A5CF6D7A5250E2C352C7D66B6A29.xml b/data/38/62/A5/3862A5CF6D7A5250E2C352C7D66B6A29.xml new file mode 100644 index 00000000000..3e991aa2d6d --- /dev/null +++ b/data/38/62/A5/3862A5CF6D7A5250E2C352C7D66B6A29.xml @@ -0,0 +1,68 @@ + + + +The ant tribe Dacetini. With a revision of the Strumigenys species of the Malgasy Region by Brian L. Fisher, and a revision of the Austral epopostrumiform genera by Steven O. Shattuck. + + + +Author + +Bolton, B. + +text + + +Memoirs of the American Entomological Institute + + +2000 + +65 + + +1 +1028 + + + + +http://hdl.handle.net/10199/15409 + +journal article +8538 +AA3AF36F-DAE3-48E6-812F-8A9934C335BE + + + + +Strumigenys vazimba Fisher +sp. n. +(Figs 399, 419) + + + +HOLOTYPE WORKER. TL 5.4, HL 1.51, HW 1.44, CI 95, ML 0.70, MI 46, SL 0.92, SI 64, PW 0.61, AL 1.29. Characters of vazimba-complex. Mandibles robust, almost straight, at full closure diverging apically. Each mandible with 1 preapical blunt tooth which is situated in the apical third of the length. Upper scrobe margin with a greatly expanded lamellate flange throughout its length, eyes not visible in full-face view. Eye small, convex, maximum diameter of eye less than maximum width of scape. Scape widest in midsection of basal half, curved in apical third; hairs on leading edge fine, narrowly spatulate. Cephalic dorsum with short curved narrowly spatulate to spoon-shaped groundpilosity; upper scrobe margin fringed with hairs similar in size and shape as those on the dorsum. Cephalic dorsum with 3 pairs (some paratypes with 4 pairs) of stout standing narrowly spatulate hairs arranged in a transverse row close to the occipital margin, and 1 pair on vertex. Dorsum of head reticulate-punctate and with superimposed rugulose sculpture. Pronotal humeral hair absent; dorsal alitrunk without erect hairs. Humeral angles rounded, posterior lateral margin of pronotum marginate and often with a raised welt. Propodeum with two pairs of short, narrowly spatulate posteriorly curved hairs at anterior base of propodeal spines. Alitrunk dorsum with short curved spatulate ground-pilosity. Dorsum of alitrunk in outline convex anteriorly, posterior portion of mesonotum sharply depressed, posterior alitrunk more or less flat. Metanotal groove shallowly impressed. Anterior margin of mesonotum raised above pronotum, forming a transverse arched lip across dorsum. Anterior mesonotum with a narrow projecting rim above the mesothoracic spiracle. Propodeal spines narrow, almost spiniform, diverging, strongly elevated and recurved anteriorly; lamella absent from declivity. Pronotal dorsum striolate-punctate to rugulose-punctate with anterior margin without punctures or with a fine punctulate surface. Sides of pronotum striolate to costulate with punctate sculpture on apical portion and more or less smooth or finely punctulate on basal half. Mesonotum and propodeum densely reticulate-punctate. Pleurae with reticulate-punctulate sculpture which is faint or effaced on central pleurae. Petiole node in dorsal view with superficial rugulose sculpture on a fine reticulate-punctulate surface, slightly broader than long. Postpetiole disc with faint longitudinally striolate sculpture on a finely punctulate surface. In profile ventral spongiform tissue of petiolar peduncle a well developed curtain along the base of the peduncle, depth of strip distinctly greater than maximum width of eye. Ventral spongiform lobe of postpetiole moderately developed. Basigastral costulae dense and distinct, interspersed with longer faint striolate sculpture. Dorsal surface of petiole with one pair of erect stout remiform hairs; postpetiole and gaster with stout standing remiform hairs. Colour light to medium brown. +PARATYPE WORKERS. TL 4.9 - 6.0, HL 1.37 - 1.66, HW 1.28 - 1.65, CI 93 - 101, ML 0.65 - 0.72, MI 43 - 48, SL 0.86 - 1.04, SI 62 - 68, PW 0.53 - 0.67, AL 1.13 - 1.44 (7 measured). As holotype. + + +Holotype worker, Madagascar: 6.3 km. S Ambanizana, Andranobe, 15 ° 41 ' S, 49 ° 57 ' E, 25 m., 14. xi. 1993, sifted litter (leaf mold, rotten wood), rainforest, # 886 (4) - 11 (B. L. Fisher) (MCZ). +Paratypes. 7 workers with same data as holotype but coded (21) - 14, (13) - 12, (46) - 11, (30) - 7, (34) - 10, (43) - 7 (BMNH, SAM). +NON-PARATYPIC MATERIAL EXAMINED. Madagascar: 6.5 km. SSW Befingotra, Res. Anjanaharibe-Sud, 875 m. (B. L. Fisher); 17 km. W Andapa, Res. Anjanaharibe-Sud, 875 m. (G. D. Alpert); 9.2 km. WSW Befingotra, Res. Anjanaharibe-Sud, 1200 m. (B. L. Fisher); 5.3 km. S Ambanizana, Andranobe, 425 m. (B. L. Fisher); 6.9 km. NE Ambanizana, 825 m. (B. L. Fisher); Andranobe, Route d'Andriamena, (A. Peyrieras); F. C. Andrianantantely, 530 m. (H. J. Raisirarson); F. C. Sandranantitra, 450 m. (H. J. Ratsirarson); 43 km. S Ambalavao, Res. Andringitra, 825 m. (B. L. Fisher); 45 km. S Ambalavao, 785 m. (B. L. Fisher); 9.0 km. NE Ivohibe, 900 m. (S. Razafimandimby); 8.0 km. E Ivohibe, R. S. Ivohibe 1200 m. (S. Razafimandimby); 10 km. NW Enakara, Res. Andohahela, 430 m. (B. L. Fisher). + + +Measurements of this material extend the range shown by the type-series: HL 1.32 - 1.45, HW 1.28 - 1.41, CI 95 - 101, ML 0.61 - 0.69, MI 46 - 50, SL 0.83 - 0.92, SI 64 - 69 (6 measured). In some specimens from Ivohibe, disc of postpetiole more or less smooth but otherwise match all characters of type-series. + + + +S. vazimba +is unmistakable. It is one of the largest known species of Strumigenys in the world (HW 1.28 - 1.65), approached only by larger individuals of the Malesian polymorphic species +loriae +(HW 1.60) and the Neotropical +godmani +(HW 1.24). In Madagascar is approached only by +grandidieri +(HW 0.97 - 1.14). The presence of only 1 preapical tooth and / or denticle on left mandible blade, the greatly expanded laminar flange along the length of the upper scrobe margin, divergent and recurved propodeal spines, and the alitrunk dorsum without erect hairs, also characterise this species. + + + + \ No newline at end of file diff --git a/data/38/62/CD/3862CD1142AA3F98A5E664B4EC09C2BB.xml b/data/38/62/CD/3862CD1142AA3F98A5E664B4EC09C2BB.xml new file mode 100644 index 00000000000..5beea26d17b --- /dev/null +++ b/data/38/62/CD/3862CD1142AA3F98A5E664B4EC09C2BB.xml @@ -0,0 +1,109 @@ + + + +New systematic assignments in Gonyleptoidea (Arachnida, Opiliones, Laniatores) + + + +Author + +Pinto-da-Rocha, Ricardo + + + +Author + +Benedetti, Alipio Rezende + + + +Author + +de Vasconcelos, Eduardo Gomes + + + +Author + +Hara, Marcos Ryotaro + +text + + +ZooKeys + + +2012 + +198 + + +25 +68 + + + + +http://dx.doi.org/10.3897/zookeys.198.2337 + +journal article +http://dx.doi.org/10.3897/zookeys.198.2337 +1313-2970-198-25 + + + + + +Gonyleptes perlatus ( +Mello-Leitao +, 1935) + +comb. n. + + + + +Moojenia perlata +Mello-Leitao +, 1935: 384, fig. 13 (♂); (2 males syntypes, Brazil, Minas Gerais, +Vicosa +, MNRJ 1577, examined) + + +Collonychium perlatum +: +Kury 2003 +: 123. + + + +Diagnosis. + +Gonyleptes perlatus +is very similar to +Gonyleptes horridus +(according to +Kury 2003 +) but can be distinguished by the relatively larger tubercles on lateral margin of the do +rsal +scutum and the absence of a robust prolateral row of apophysis on male femur IV (present in +Gonyleptes horridus +), although this article might present variable armature. + + + +Taxonomical note. + +We propose the allocation of this species in +Gonyleptes +because it is very similar to +Gonyleptes horridus +(see comments in +Kury 2003 +), including the typical sexual dimorphism. According +Kury (2003) +, both species are allopatric. + + + + \ No newline at end of file diff --git a/data/38/62/E8/3862E8BA3793579A8CB6B1B410E8B8ED.xml b/data/38/62/E8/3862E8BA3793579A8CB6B1B410E8B8ED.xml new file mode 100644 index 00000000000..181ca821712 --- /dev/null +++ b/data/38/62/E8/3862E8BA3793579A8CB6B1B410E8B8ED.xml @@ -0,0 +1,408 @@ + + + +A taxonomic revision of the freshwater crab genus Parvuspotamon Dai & Bo, 1994 (Decapoda, Brachyura, Potamidae), with descriptions of a new genus and two new species + + + +Author + +Shi, Boyang +https://orcid.org/0000-0003-3306-3764 +Jiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China + + + +Author + +Pan, Da +https://orcid.org/0000-0001-5445-6423 +Jiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China +dapan@njnu.edu.cn + + + +Author + +Sun, Hongying +https://orcid.org/0000-0003-2311-1814 +Jiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China +sunhongying@njnu.edu.cn + +text + + +ZooKeys + + +2023 + +2023-10-26 + + +1183 + + +13 +38 + + + + +http://dx.doi.org/10.3897/zookeys.1183.109948 + +journal article +http://dx.doi.org/10.3897/zookeys.1183.109948 +1313-2970-1183-13 +DA6935B9D9E14B0B86867B661CB9140E +BDA133EB90F858529CF6B98DF9DF64EE + + + + +Parvuspotamon yuxiense Dai & Bo, 1994 + + + + +Figs 2 +, 3 +, 4 + + + +Type material. + + +Holotype +. + +China • ♂, 15.7 +x +12.9 mm; Yunnan Province, Yuxi City, Xinping County, Gasa Township; Aug. 1990; CB05138 YN 9091116A. + + + +Additional material. + + +China +• +4 ♂ +, 26.18 +x +19.73 mm +(NNU-3151-01), 23.26 +x +17.19 mm +(NNU-3151-02), 22.68 +x +17.02 mm +(NNU-3151-03), 20.79 +x +15.52 mm +(NNU-3151-04) + +, + +3 ♀ +, 22.82 +x +16.98 (NNU-3151-05), 21.13 +x +16.47 (NNU-3151-06), 22.59 +x +17.35 (NNU-3151-07); +Yunnan Province +, +Yuxi City +, +Xinping County +, +Heshalak Village +; +23.96°N +, +101.45°E +; altitude + +955 m +asl + +; +11 Apr. 2019 +; +Boyang Shi +, +Xiyang Hao +, +Zewei Zhang +, and +Hongying Sun +, leg. + +• +5 ♂ +, 24.94 +x +18.94 mm +(NNU-1513-01), 21.16 +x +16.86 mm +(NNU-1513-02), 22.02 +x +16.06 mm +(NNU-1513-03), 18.72 +x +13.42 mm +(NNU-1513-04), 16.58 +x +11.98 mm +(NNU-1513-05), + +2 ♀ +, 22.54 +x +16.63 mm +(NNU-1513-06), 17.12 +x +12.77 mm +(NNU-1513-07); +Yunnan Province +, +Yuxi City +, +Gasha Town +; +24.02°N +, +101.58°E +; altitude + +795 m +asl + +; +15 Oct. 2015 +; +Kelin Chu +, +Qiang Zhao +, +Pengfei Wang +, and +Hongying Sun +leg. + + + + +Description. + +Medium sized (adult carapace width 16-26 mm, +n += 15). Carapace broader than long, ovate; dorsal surface convex both transversely and longitudinally, smooth, regions not clear; branchial regions swollen, smooth (Figs +2A +, +4A +). Postorbital and epigastric cristae confluent (Figs +2A +, +4A +); epigastric cristae weakly developed, oblique, separated by deep inverted Y-shaped groove (Figs +2A +, +4A +); postorbital cristae low, indistinct (Figs +2A +, +4A +). External orbital angle bluntly triangular, outer margin and anterolateral margin of carapace confluent (Figs +2A +, +4A +). Anterolateral margin of carapace entire convex, smooth; posterolateral margin gently concave, smooth, converging towards posterior carapace margin (Figs +2A +, +4A +). Epibranchial tooth indistinct (Figs +2A +, +4A +). Orbits large; supraorbital and infraorbital margins smooth; sub-orbital, sub-hepatic, and pterygostomial regions smooth (Figs +2B, C +, +4B, C +). Antennular fossae slit-like in anterior view; median lobe of epistome posterior margin narrowly triangular (Figs +2B +, +4B +). Third maxilliped with rhombus ischium; exopod reaching beyond anterolateral corner of ischium, without flagellum (Fig. +3G +). + + +Chelipeds unequal (Figs +2A-C +, +3A, B +, +4A-C +). Merus trigonal in cross section; margins weakly crenulated (Figs +2A +, +4A +). Carpus with sharp spine at inner-distal angle (Figs +2A +, +4A +). Major cheliped palm length ~ 1.3 +x +height (Fig. +3B +). Occlusal margin of fingers with several small teeth; distinct gape when closed (Fig. +3A, B +). + + +Ambulatory legs not distinctly elongated, dactyli slender (Figs +2A, C +, +4A, C +); second pair longest, last pair shortest (Figs +2A, C +, +4A, C +). Outer surface of merus weakly rugose, dorsal margin weakly serrated, without subdistal tooth, length ~ 4.1 +x +width (Figs +2A +, +4A +). + + +Male thoracic sternum smooth, weakly pitted; sternites 1/2 fused forming triangular structure; sternites 2/3 separated by deep but incomplete groove; sternites 3/4 completely fused; median longitudinal suture of sternites 7/8 deep (Figs +2C +, +3C, E +, +4C +). Vulvae transversely ovate, widely located from each other, touching suture of sternites 5/6, posteromesial margin with low rim, opened obliquely upwards (Fig. +3F +). + + +Male pleon broadly triangular; male telson relatively broad, lateral margins concave, width ~ 1.4 +x +length; male pleonal somite 6 trapezoidal, broad, width ~ 2.3 +x +length; somites 3-5 trapezoidal, gradually decreasing in width; somite 2 trapezoidal, reaching to bases of coxae of fourth ambulatory legs, thoracic sternite 8 not visible when pleon closed (Figs +2C +, +3C +, +4C +). Female pleon ovate, covering most of thoracic sternum (Fig. +3D +). + + +G1 slender, reaching pleonal locking tubercle +in situ +, with terminal and subterminal segments clearly demarcated (Figs +3E, H, I +, +4D-G +); subterminal segment stout, slightly sinuous (Figs +3H, I +, +4D, E +); terminal segment slender, relatively long, subconical, strongly sinuous, bent inwards, inner margin strongly concave, ~ 0.6 +x +length of subterminal segment, without groove for G2 on ventral side, tip rounded, dorsal flap absent (Figs +3H, I +, +4D-G +). G2 longer than G1; terminal segment relatively long; subterminal segment ~ 1.5 +x +length of terminal segment (Fig. +3J +). + + + +Colour in life. +Carapace and chelipeds are generally yellowish brown in mature individuals. + + +Habitat. + + +Parvuspotamon yuxiense + +can be found under rocks in hill streams at ~ 700-1000 m altitude. + + + +Remarks. + + +Parvuspotamon yuxiense + +is the sole species of the genus and closely related to the species of + +Songpotamon + +gen. nov., and two species of + +Tenuipotamon + +Dai, 1990 ( + +Tenuipotamon yuxiense + +Chen, 1993, and + +Tenuipotamon xingpingense + +Chen, 1993) that are known from Xinping County, Yuxi City of Yunnan Province. + +Parvuspotamon yuxiense + +can nevertheless be differentiated from + +T. yuxiense + +and + +T. xingpingense + +by the following characters: anterolateral margins of the carapace entire and smooth (vs cristate); and G1 terminal segment relatively less strongly curved, lacking a dorsal flap (vs more strongly curved, with a distinct dorsal flap) [cf. +Chen 1993 +: figs 3 (4-6), 4 (4-6)]. On the other hand, + +P. yuxiense + +can be differentiated from the species of + +Songpotamon + +gen. nov. by the characters in the carapace, vulvae and G1 (see Remarks for + +Songpotamon + +gen. nov.). + + + +Geographic distribution. + + +Parvuspotamon yuxiense + +is known only from the Yuxi City, Yunnan Province, southwest China. + + + + \ No newline at end of file diff --git a/data/38/63/06/386306D3631B9C8ECCC7AF3B8F9567AD.xml b/data/38/63/06/386306D3631B9C8ECCC7AF3B8F9567AD.xml new file mode 100644 index 00000000000..15ebcf93a97 --- /dev/null +++ b/data/38/63/06/386306D3631B9C8ECCC7AF3B8F9567AD.xml @@ -0,0 +1,76 @@ + + + +Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea + + + +Author + +Dale-Skey, Natalie + + + +Author + +Askew, Richard R. + + + +Author + +Noyes, John S. + + + +Author + +Livermore, Laurence + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8013 +8013 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8013 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8013 +1314-2828--8013 + + + + +Eustochus atripennis (Curtis, 1832) + + + + +Mymar atripennis +Curtis, 1832 + + + +Distribution +England + + + \ No newline at end of file diff --git a/data/38/63/8F/38638F37FFDD2DE7F854B9933F39E2F5.xml b/data/38/63/8F/38638F37FFDD2DE7F854B9933F39E2F5.xml new file mode 100644 index 00000000000..05dca834dd4 --- /dev/null +++ b/data/38/63/8F/38638F37FFDD2DE7F854B9933F39E2F5.xml @@ -0,0 +1,50 @@ + + + +Leptocephali collected off the eastern coast of Brazil (12 ° – 23 ° S). + + + +Author + +Marcia Salustiano de Castro + + + +Author + +Ana Cristina Teixeira Bonecker + +text + + +Zootaxa + + +2005 + +935 + + +1 +28 + + + + +http://www.zoobank.org/urn:lsid:zoobank.org:pub:3EA0A64C-D816-4404-8602-B8A4A37D170E + +journal article +z00935p001 +3EA0A64C-D816-4404-8602-B8A4A37D170E + + + + +Study Material - +Bascanichthys +sp.: DZUFRJ 2920; one specimen; total myomeres 176; 49.5 mm SL. + + + + \ No newline at end of file diff --git a/data/38/63/AE/3863AE580A2858E7B71ADE760146D5E3.xml b/data/38/63/AE/3863AE580A2858E7B71ADE760146D5E3.xml new file mode 100644 index 00000000000..422174f108f --- /dev/null +++ b/data/38/63/AE/3863AE580A2858E7B71ADE760146D5E3.xml @@ -0,0 +1,66 @@ + + + +Catalogue of Geadephaga (Coleoptera, Adephaga) of America, north of Mexico + + + +Author + +Bousquet, Yves +Agriculture and Agri-Food Canada, Central Experimental Farm, Ottawa, Ontario, Canada +bousquety1@yahoo.com + +text + + +ZooKeys + + +2012 + +2012-11-28 + + +245 + + +1 +1722 + + + + +http://dx.doi.org/10.3897/zookeys.245.3416 + +journal article +http://dx.doi.org/10.3897/zookeys.245.3416 +1313-2970-245-1 +FFFF52503A0AFF882450FFB66D45FF8E +578462 + + + + +Ellipsoptera nevadica tubensis (Cazier, 1939) + + + + +Cicindela nevadica tubensis +Cazier, 1939: 25. Type locality: "Tuba City, Coconino Co[unty], Arizona" (original citation). Holotype (♀) probably in AMNH. + + + +Distribution. +This subspecies, the "Tube Tiger Beetle", ranges from northeastern Utah to central Arizona and northwestern New Mexico [see Willis 1967: Fig. 143]. + + +Records. + +USA +: AZ, CO, NM, UT + + + + \ No newline at end of file diff --git a/data/38/64/34/38643471FF908A2285881E42FD07FBD9.xml b/data/38/64/34/38643471FF908A2285881E42FD07FBD9.xml new file mode 100644 index 00000000000..7f07ce392ae --- /dev/null +++ b/data/38/64/34/38643471FF908A2285881E42FD07FBD9.xml @@ -0,0 +1,237 @@ + + + +Demystifying three species of Ctenidae (Arachnida: Araneae) described by Embrik Strand. Part I, Ecuador + + + +Author + +Dupérré, Nadine + +text + + +Zootaxa + + +2014 + +3784 + + +1 + + +67 +73 + + + +journal article +36879 +10.11646/zootaxa.3784.1.3 +830784dc-7050-4956-9086-c87910d188e5 +1175-5326 +285803 +79EB8DEC-B2B3-4778-9A74-4A40184E872B + + + + + + + +Enoploctenus inazensis +( +Strand, 1909 +) + + + + + +Figs 4–8 +. + + + + + + +Ctenus inazensis + +Strand 1909 +: 307 + + +. + + + + + +Enoploctenus inazensis +(Strand) + +; + +Polotow and Brescovit 2014 +: 359 + +. + + + + + + +Type +material: + +Label 1: Species: + +Ctenus inazensis +Strand. Fundort + +: +1♂ +1♀ +Syntypes +, +Ecuador +, Santa Inaz. Leg. R. Haensch, Marz 1899. Det. +Strand 1909 +. Zool. Mus. Berlin: Kat Nr. 30658. Label 2: M. 71, R. Haensch. Santa Inaz. +Ecuador +, Marz 1899. Label 3: + +Ctenus inazensis +Strand + +[ +Types +!]. (Deposited +ZMB +) EXAMINED. + + + + +Diagnosis. +Females can be distinguished from all +Ctenidae +by the quadrangular median sector of the epigynum and the basal position of the lateral spurs ( +Fig. 4 +); males can be diagnosed from all +Ctenidae +by the embolus base bearing two curved prongs and the elongated median apophysis ( +Fig. 7 +). + + + + +FIGURES 4–8. + +Enoploctenus inazensis +Strand, 1909 + +. Female 4–6. Male 7–8. +4. +Holotype, epigynum ventral view. +5. +Holotype, internal genitalia dorsal view. +6. +Holotype, carapace dorsal view. +7. +Syntype, palp ventral view. +8. +Syntype, palp tibia retrolateral view. Abbreviations: c, conductor; cd, copulatory ducts; e, embolus; fd, fertilization ducts; ls, lateral spurs; ma, median apophyis; ms, median sector; rta, retrolateral tibial apophysis; rtn; retroapical tibial notch; s, spermathecae. Scale bars figures 4, 5: 0.5mm; figures 6–8: 1.0mm. + + + + + +Description. +Female +: + +Total length: 24; carapace length: 10; carapace width: 7.8. CEPHALOTHORAX: Carapace brown suffused with gray along radiating lines and on pars cephalica ( +Fig. 6 +); pyriform; fovea long; covered with long white setae. Clypeus low ( +2 x +AME). Sternum dark brown, as long as wide. Endites longer than wide; labium not notch. Chelicerae dark reddish-brown, geniculate; promargin with three teeth and retromargin four to five teeth. EYES: Eight in three rows; AME rounded, separated by half their width; PME rounded, separated by half their width; AME-PME separated by half the width of AME; ALE rounded, small close to PLE; PLE rounded. ABDOMEN: Light brown, elongated oval; with remnant patches of long white and black short setae LEGS: Orange-brown with dark gary pattern; leg spination damaged, not examined (see +Strand 1909 +: 307, 308); metatarsus IV unmodified; tarsal claw with one large and five small tooth; claw tufts presents. Palpal claw with five large teeth and one small tooth. GENITALIA: Epigynum with elongated median sector, squared in the middle; lateral spurs positioned basally ( +Fig. 4 +). Internal genitalia: copulatory ducts long; spermathecae globular; fertilization ducts short, situated on the inner side at the base of the spermathecae ( +Fig. 5 +). + + + +Male +. + +Total length: 13; carapace length: 7; carapace width: 5. CEPHALOTHORAX: as in female. Chelicerae dark reddish-brown, geniculate; promargin three and retromargin four tooth. EYES: as in female. LEGS: Damaged, not examined (see +Strand 1909 +: 308); metatarsus IV unmodified. ABDOMEN: Light beige, elongated oval. GENITALIA: Palpal tibia elongated, more or less equal to the cymbium ( +Fig 7 +); retrolateral tibial apophyis short and pointed ( +Fig. 8 +): retroapical tibial notch present ( +Fig. 7 +). Palpal cymbium pointed ( +Fig.7 +). Embolus elongated, with wide and transparent tip; base of embolus with two prongs; median apophysis elongated with curved tip; conductor white, small and oval ( +Fig. 7 +). + + + + +Other material examined. +Label 1: Species: + +Ctenus inazensis +Strand. Label + +2: Santa Inaz, +Ecuador +, Marz 1899. M.71. R. Haensch. Lable 3: Zool. Mus. Berlin: Kat Nr. 30659. 1♀ +Syntypes +. + + +Notes. +Polotow and Brescovit (2014: 359) +transferred + +C. inazensis + +to + +Enoploctenus +Simon, 1897 + +based on the results of their morphological cladistic analysis ( +Polotow and Brescovit 2014: figs 1, 2 +). In addition, they proposed a synapomorphic character for the genus + +Enoploctenus + +, the presence of a retroapical tibial notch of the male palpal tibia ( +Polotow and Brescovit 2014: 8 +). + + + + +Distribution. +Ecuador +, Tungurahua province. + + + + \ No newline at end of file diff --git a/data/38/64/34/38643471FF938A2485881D49FC11FE69.xml b/data/38/64/34/38643471FF938A2485881D49FC11FE69.xml new file mode 100644 index 00000000000..fe88337e2e2 --- /dev/null +++ b/data/38/64/34/38643471FF938A2485881D49FC11FE69.xml @@ -0,0 +1,179 @@ + + + +Demystifying three species of Ctenidae (Arachnida: Araneae) described by Embrik Strand. Part I, Ecuador + + + +Author + +Dupérré, Nadine + +text + + +Zootaxa + + +2014 + +3784 + + +1 + + +67 +73 + + + +journal article +36879 +10.11646/zootaxa.3784.1.3 +830784dc-7050-4956-9086-c87910d188e5 +1175-5326 +285803 +79EB8DEC-B2B3-4778-9A74-4A40184E872B + + + + + + + +Ctenus datus +Strand 1909 + + + + + +Figs 1–3 +. + + + + + + +Ctenus datus + +Strand 1909 +: 316 + + +. + + + + + + +Type +material. + +Label 1: Species: + +Ctenus datus +Strand. Fundort + +: 1♀ +Holotype +(Cotype), Cachabé. Leg. Rosenberg, +29.9.1898 +. Det. +Strand 1909 +. Zool. Mus. Berlin: Kat Nr. 30656. Label 2: Cachabé. Von Herrn Rosenberg in London. +28- 9-1898 +. Label 3: + +Ctenus datus +Strand + +[ +Type +!]. (Deposited +ZMB +) EXAMINED. + + + + +Diagnosis. +Females can be distinguished from all other + +Ctenus + +species by the shape of the ovoid lobes ( +Figs 1, 2 +); from + +C. amphora + +by the ovoid lobes separated by a deep to shallow groove ( +Figs 1, 2 +) without space; from + +C. vehemens + +by the oval spermathecae ( +Fig. 3 +), rounded in the later. + + + + +Description. +(specimen faded): + +Female +: + +Total length: 14.3; carapace length: 6.1; carapace width: 4.9. CEPHALOTHORAX: Carapace orange, slightly darker along radiating lines; pyriform; fovea long; covered with short white setae. Clypeus low ( +1 x +AME). Sternum light orange, as long as wide. Endites longer than wide; labium not notched. Chelicerae dark reddish-brown, geniculate; promargin with three teeth and retromargin with five teeth. EYES: Eight in three rows; AME rounded, separated by half their width; PME rounded, separated by half their width; AME- PME separated by half the width of AME; ALE oval, small close to PLE; PLE rounded. ABDOMEN: Light beige, elongated oval. LEGS: Orange; leg spination damaged, not examined (see +Strand 1909 +: 317); metatarsus IV unmodified; tarsal claw with one large and two to three small tooth; claw tufts presents. Palpal claw with four large teeth and one small tooth. GENITALIA: Epigynum with large ovoid lobes separated by deep ( +Fig. 1 +) to shallow groove ( +Fig. 2 +); median sector bulbous and dark ( +Figs 1, 2 +); lateral spurs positioned medially ( +Figs 1, 2 +). Internal genitalia: copulatory ducts large; spermathecae oval; fertilization ducts curved, situated on the outer side at the base of the spermathecae ( +Fig. 3 +). + + + +Male +. + +Unknown. + + + + +Other material examined. +None. + + +Notes. +This species clearly belongs to the genus + +Ctenus + +due to the presence of large ovoid lobes of the epigynum. + + + + +Distribution. +Ecuador +, Esmeraldas Province, San Javier de Cachabi. + + + + \ No newline at end of file diff --git a/data/38/64/34/38643471FF938A2785881C01FA2EFACC.xml b/data/38/64/34/38643471FF938A2785881C01FA2EFACC.xml new file mode 100644 index 00000000000..98eb5551e9a --- /dev/null +++ b/data/38/64/34/38643471FF938A2785881C01FA2EFACC.xml @@ -0,0 +1,74 @@ + + + +Demystifying three species of Ctenidae (Arachnida: Araneae) described by Embrik Strand. Part I, Ecuador + + + +Author + +Dupérré, Nadine + +text + + +Zootaxa + + +2014 + +3784 + + +1 + + +67 +73 + + + +journal article +36879 +10.11646/zootaxa.3784.1.3 +830784dc-7050-4956-9086-c87910d188e5 +1175-5326 +285803 +79EB8DEC-B2B3-4778-9A74-4A40184E872B + + + + + + + +Ctenus +Walckenaer 1805 + + + + + + + +Type +species + +Ctenus dubius +Walckenaer 1805 + + + + + +Diagnosis. +Brescovit & Simó (2007: 2) +provided a diagnosis for the genus + +Ctenus + +as follows: Males with short palpal tibia; tegulum elongated basally; embolus with a basal projection; median apophysis short and truncated apically. Female epigynum with anterior protruding ovoid lobes; epigynum with conspicuous lateral spurs positioned medially to basally. + + + + \ No newline at end of file diff --git a/data/38/64/34/38643471FF968A2385881C7EFD07FF19.xml b/data/38/64/34/38643471FF968A2385881C7EFD07FF19.xml new file mode 100644 index 00000000000..22b11b61df1 --- /dev/null +++ b/data/38/64/34/38643471FF968A2385881C7EFD07FF19.xml @@ -0,0 +1,175 @@ + + + +Demystifying three species of Ctenidae (Arachnida: Araneae) described by Embrik Strand. Part I, Ecuador + + + +Author + +Dupérré, Nadine + +text + + +Zootaxa + + +2014 + +3784 + + +1 + + +67 +73 + + + +journal article +36879 +10.11646/zootaxa.3784.1.3 +830784dc-7050-4956-9086-c87910d188e5 +1175-5326 +285803 +79EB8DEC-B2B3-4778-9A74-4A40184E872B + + + + + + + +Ctenus satanas +Strand, 1909 + + + + + +Figs 9–10 +. + + + + + + +Ctenus satanas + +Strand, 1909 +: 320 + + +. + + + + + + +Type +material. + +Label 1: Species: + +Ctenus satanas +Strand. Fundort + +: 1♀ +Holotypus +, +Ecuador +, Santa Inaz. Leg. R. Haensch, Marz 1899. Det. +Strand 1909 +. Zool. Mus. Berlin: Kat Nr. 30654. Label 2: Santa Inaz. +Ecuador +, Marz 1899. M.71, R. Haensch. Label 3: + +Ctenus satanas +Strand + +[ +Type +!]. (Deposited +ZMB +) EXAMINED. + + + + +Diagnosis +. Females can be diagnosed from all +Ctenidae +by the short and squared median lobe of the epigynum ( +Fig. 9 +). + + + + + +Description. +Female +: + +Total length: 17; carapace length: 8; carapace width: 7. CEPHALOTHORAX: Carapace orange-brown suffused with gray along radiating lines and on pars cephalica; fovea long. Clypeus low ( +1 x +AME). Sternum light brown, as long as wide. Endites longer than wide; labium not notch. Chelicerae dark reddish-brown, geniculate; promargin and retromargin with four teeth. EYES: Eight in three rows; AME rounded, separated by half their width; PME rounded, separated by half their width; AME-PME separated by half the width of AME; ALE oval, small close to PLE; PLE rounded. ABDOMEN: Light brown, elongated oval; with white median stripe. LEGS: Orange-brown with stripes of dark gray; legs spination damaged, not examined (see +Strand 1909 +: 320); metatarsus IV unmodified; tarsal claw with three teeth; claw tufts presents. GENITALIA: Epigynum with median sector excavated, with squared median lobe; lateral spurs positioned medially; large, basal lateral lobes ( +Fig. 9 +). Internal genitalia: copulatory ducts long; head of spermathecae oval; base of spermathecae c-shaped; fertilization ducts short and wide, situated at end of the c-shaped spermathecae base ( +Fig. 10 +). + + + +Male +. + +Unknown. + + +Notes. +This species does not belong in + +Ctenus + +, but I am unable to place it with certainty in any other genus. I feel it is better to leave it in + +Ctenus + +for now. The morphological cladistic analysis of +Polotow and Brescovit 2014 +(figs 1, 3) also confirmed that + +C. satanas + +does not belong in the genus + +Ctenus +. + +Furthermore, it probably needs to be placed in a new genus along with a new species from +Brazil +(D. Polotow pers. comm). + + + + +Other material examined. +None. + + + + +Distribution. +Ecuador +, Tungurahua province. + + + + \ No newline at end of file diff --git a/data/38/64/42/386442F097E907A2072E5DFCA1499361.xml b/data/38/64/42/386442F097E907A2072E5DFCA1499361.xml new file mode 100644 index 00000000000..0f2871a7c1b --- /dev/null +++ b/data/38/64/42/386442F097E907A2072E5DFCA1499361.xml @@ -0,0 +1,58 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828--9042 + + + + +Apsilops aquaticus (Thomson, 1874) + + + + +Trichocrytus aquaticus +Thomson, 1874 + + +napiformis +(Rudow, 1882, +Cryptus +) + + + +Distribution +England + + + \ No newline at end of file diff --git a/data/38/65/15/38651521665F11E7DB257A9A066C7497.xml b/data/38/65/15/38651521665F11E7DB257A9A066C7497.xml new file mode 100644 index 00000000000..b89adaa1f5f --- /dev/null +++ b/data/38/65/15/38651521665F11E7DB257A9A066C7497.xml @@ -0,0 +1,173 @@ + + + +Shallow-water zoantharians (Cnidaria, Hexacorallia) from the Central Indo-Pacific + + + +Author + +Reimer, James D. + + + +Author + +Poliseno, Angelo + + + +Author + +Hoeksema, Bert W. + +text + + +ZooKeys + + +2014 + +444 + + +1 +57 + + + + +http://dx.doi.org/10.3897/zookeys.444.7537 + +journal article +http://dx.doi.org/10.3897/zookeys.444.7537 +1313-2970-444-1 +FB83BDD3958A456DBFEA9C6C28D3E4D5 + + + +Taxon classification Animalia Zoantharia Epizoanthidae + + + +24. +Epizoanthus aff. illoricatus Tischbierek, 1930 +Figures 20B, 21 + + + + +Specimens + + +(n=2). RMNH Coel 40536, +Snellius-II +Station 4.058, east of Melolo, northeast Sumba ( +09°51'S +, +120°45'E +), depth = 180 m, collected on September 14, 1984 by rectangular dredge; RMNH Coel 40547, +Snellius-II +Station 4.051, east of Melolo, northeast Sumba ( +09°53'30"S +, +120°42'42"E +), depth = 75 to 90 m, collected on September 13, 1984 by rectangular dredge. + + + +Photographic records + +(n=12). Desa Ped, north Nusa Penida, east Bali ( +08°40'28"S +, +115°30'50"E +), May 28, 1998; 4 specimens from Tulamben, east Bali ( +08°16'26"S +, +115°35'28"E +), July 9-10, 1997; Nusa Penida, east Bali, ( +08°40'23"S +, +115°29'13"E +), May 27, 1998; Kapoposang, Spermonde Archipelago, South Sulawesi ( +04°41'40"S +, +118°54'55"E +), June 24, 1997, August 8, 1997; west Pulau Samalona, Spermonde Archipelago, South Sulawesi ( +05°07'30"S +, +119°20'15"E +), September 16, +1997 +; Fauna Malesiana Maluku Expedition station MAL.10, south coast of Ambon Bay, east of Eri, Ambon ( +03°45'S +, +128°08'E +), November 12, 1996; Maluku Expedition station MAL.12, north coast near Morela, Ambon ( +03°33'S +, +128°12'E +), November 13-14, 1996; Maluku Expedition station MAL.19, Tanjung Batu Dua, east of Hatu, north coast Ambon Bay, Ambon ( +03°43'S +, +128°03'E +), November 19, 1996; Fauna Malesiana Marine Sulawesi Expedition station SUL.16, bay east of Tanjung Labuhankompeni, Pulau Lembeh, Lembeh Strait, North Sulawesi +( +01°26'N +, +125°11'E +), October 23, 1994; west Pulau Siladen, Bunaken, North Sulawesi ( +01°38'N +, +124°46'E +), May 2, 1998. + + + +Description. + +Azooxanthellate. As +Epizoanthus illoricatus +above, obligate epibiont on eunicid worms. Polyps of this putative species are at least twice as big in diameter as +Epizoanthus illoricatus +(average 2.1 mm, compared with a maximum of 2 mm for +Epizoanthus illoricatus +), and many times bigger in terms of volume. Additionally, both specimens have brown coenenchyme and scapus, different from the light gray coenenchyme and brownish oral disk reported for +Epizoanthus illoricatus +(Figure 20B). In situ images show colonies with cream, brown, red-brown, orange-brown or tan coenenchyme and scapus, often with white tentacles that are comparatively shorter and thicker than in +Epizoanthus illoricatus +. The coenenchyme of this putative species is much more developed than +Epizoanthus illoricatus +, with polyps arising from not only bends of the zig-zag shaped eunicid tube, but also from other locations. The result is a colony that has a higher density of polyps than +Epizoanthus illoricatus +. In +Epizoanthus illoricatus +, often the zig-zag shape of the eunicid tube is visible between polyps, but this is rarely the case in +Epizoanthus aff. illoricatus +(Figure 20B). + + + + +Distribution +. + +Regions recorded in this study (Figure 21): East Bali (5), northeast Sumba (6), Spermonde Archipelago (9), Moluccas (14), Lembeh Strait (17), Bunaken (18). +Past records. NA. + + +Remarks. + +Although the two specimens here were found at deeper depths (75 to 190 m), numerous photographic records show that this species and +Epizoanthus illoricatus +have an overlapping depth range. Examination of DNA sequences combined with detailed morphological analyses should help clear up the relationship between this putative species and +Epizoanthus illoricatus +, although preliminary molecular analyses show differences between the two groups (H. Kise and J.D. Reimer, unpubl. data). It is likely records and museum specimens identified as +Epizoanthus illoricatus +from the central Indo-Pacific include both types mentioned in this study. + + + + \ No newline at end of file diff --git a/data/38/65/87/3865878FFF22C12DFF75FF6EA7F5580B.xml b/data/38/65/87/3865878FFF22C12DFF75FF6EA7F5580B.xml new file mode 100644 index 00000000000..1710f8f974f --- /dev/null +++ b/data/38/65/87/3865878FFF22C12DFF75FF6EA7F5580B.xml @@ -0,0 +1,193 @@ + + + +Additions to the knowledge of the Tribe Alyssontini (Hymenoptera: Crabronidae Bembicinae) in India with description of two new species of the genus Alysson Panzer + + + +Author + +Kumar, P. Girish +0000-0003-2121-0165 +Western Ghats Regional Centre, Zoological Survey of India, Eranhipalam, Kozhikode, Kerala- 673006, India. kpgiris @ gmail. com; https: // orcid. org / 0000 - 0003 - 2121 - 0165 +kpgiris@gmail.com + + + +Author + +Sheela, S. +Zoological Survey of India, M-Block, New Alipore, Kolkata, West Bengal- 700053, India. + + + +Author + +Sharma, Gaurav +0000-0003-2644-8797 +Northern Regional Centre, Zoological Survey of India, 218, Kaulagarh Road, Dehra Dun, Uttarakhand- 248195, India. drgaurav. sharma @ gov. in; https: // orcid. org / 0000 - 0003 - 2644 - 8797 +drgaurav.sharma@gov.in + +text + + +Zootaxa + + +2020 + +2020-10-16 + + +4861 + + +2 + + +270 +280 + + + +journal article +9026 +10.11646/zootaxa.4861.2.7 +af129ee5-c45e-4f33-bdfc-4c14402580e4 +1175-5326 +4416251 +C012766D-090F-491D-85CB-2A7BB388E885 + + + + + + + +Alysson triangularis +Krombein, 1985 + + + + + + + +( +Figs 21–30 +) + + + + + +Alysson triangularis + +Krombein, 1985:13 + + +, + +, + +. +Holotype +: + +, +Sri Lanka +: +Central Province +: +Kandy District +: +Kandy +- Udawat- takele +Sanctuary +(USNM). + + + + +Material examined +. + + +India + +: + +Tamil Nadu + +, +Coimbatore district +, +Sedivayal +near +Siruvani +( +10° 57’ 4.09’’ N +& +76° 43’ 30.93’’ E +, + +474 m + +), + + +3♀ +, + +5.i.2019 + +, +Coll. P. Girish Kumar +, +ZSIK +Regd. Nos. ZSI/ +WGRC +/IR/INV.14406–14408; Coim- batore district, valley of Palamalai Hills ( +11° 9’ 25.01’’ N +& +76° 53’ 42.22’’ E +, + +467 m + +), +4♀ +, + +6.i.2019 + +, +Coll. P. Girish Kumar +, +ZSIK +Regd. Nos. +ZSI/ +WGRC +/IR/INV.14409–14412 + +. + + + + +Distribution +. +India +(new records): +Tamil Nadu +; +Sri Lanka +( +Krombein, 1985 +) ( +Fig 41 +). + + + + \ No newline at end of file diff --git a/data/38/65/87/3865878FFF22C12FFF75FA1BA2B25AD0.xml b/data/38/65/87/3865878FFF22C12FFF75FA1BA2B25AD0.xml new file mode 100644 index 00000000000..6e9ac633a92 --- /dev/null +++ b/data/38/65/87/3865878FFF22C12FFF75FA1BA2B25AD0.xml @@ -0,0 +1,320 @@ + + + +Additions to the knowledge of the Tribe Alyssontini (Hymenoptera: Crabronidae Bembicinae) in India with description of two new species of the genus Alysson Panzer + + + +Author + +Kumar, P. Girish +0000-0003-2121-0165 +Western Ghats Regional Centre, Zoological Survey of India, Eranhipalam, Kozhikode, Kerala- 673006, India. kpgiris @ gmail. com; https: // orcid. org / 0000 - 0003 - 2121 - 0165 +kpgiris@gmail.com + + + +Author + +Sheela, S. +Zoological Survey of India, M-Block, New Alipore, Kolkata, West Bengal- 700053, India. + + + +Author + +Sharma, Gaurav +0000-0003-2644-8797 +Northern Regional Centre, Zoological Survey of India, 218, Kaulagarh Road, Dehra Dun, Uttarakhand- 248195, India. drgaurav. sharma @ gov. in; https: // orcid. org / 0000 - 0003 - 2644 - 8797 +drgaurav.sharma@gov.in + +text + + +Zootaxa + + +2020 + +2020-10-16 + + +4861 + + +2 + + +270 +280 + + + +journal article +9026 +10.11646/zootaxa.4861.2.7 +af129ee5-c45e-4f33-bdfc-4c14402580e4 +1175-5326 +4416251 +C012766D-090F-491D-85CB-2A7BB388E885 + + + + + + + +Analysson rufescens +Krombein, 1985 + + + + + + + +( +Figs 31–40 +) + + + + + +Analysson rufescens + +Krombein, 1985:9 + + +, + +, + +. +Holotype +: + +, +Sri Lanka +: +Uva Province +: +Monaragala District +: +Angunakolapelessa +(USNM). + + + + +Material examined +. + + +India + +: + +Chhattisgarh + +, +Sukma district +, +Konta +( +17° 48’ 33’’ N +& +81° 23’ 04’’ E +, + +52 m + +), +1♀ +, + +7.x.2012 + +, +Coll. Mandal +& party, +ZSIK +Regd. No. +ZSI/ +WGRC +/IR/INV.14413 + +. + + +Jharkhand + +, +Pakur district +, +Toray river +side ( +24° 37’ 53’’ N +& +87° 51’ 07’’ E +, + +32 m + +), +1♀ +, + +9.xi.2009 + +, +Coll. +R +. +Babu +& party, +ZSIK +Regd. No. +ZSI/ +WGRC +/IR/ INV.14414 + +. + + +Karnataka + +, +Kodagu district +, +Thondoor +( +12° 25’ 8.60’’ N +& +75° 52’ 74.33’’ E +, + +884 m + +), +2♀ +, + +22.xii.2019 + +, +Coll. P. Girish Kumar +, +ZSIK +Regd. Nos. +ZSI/ +WGRC +/IR/INV.14415 & 14416 + +. + + +Tamil Nadu + +, +Coimbatore district +, valley of +Palamalai Hills +( +11° 9’ 25.01’’ N +& +76° 53’ 42.22’’ E +, + +467 m + +), + + +1♀ +, + +6.i.2019 + +, +Coll. P. Girish Kumar +, +ZSIK +Regd. No. +ZSI/ +WGRC +/IR/INV.14417; +Coimbatore district +, Kottur near Anamalai Hills ( +10° 28’ 48.18’’ N +& +76° 86’ 10.85’’ E +, + +320 m + +), +1♂ +, + +2.i.2019 + +, +Coll. P. Girish Kumar +, +ZSIK +Regd. No. +ZSI/ +WGRC +/IR/INV.14418 + +. + + + + +FIGURE 42. +Distribution map of the genus + +Analysson +Krombein. + + + + + +FIGURE 43. +Distribution map of the genus + +Didineis +Wesmael + +from the Oriental region. + + + + +Distribution +. +India +: +Chhattisgarh +(new record), +Jharkhand +(new record), +Karnataka +, +Tamil Nadu +; +Sri Lanka + + +( +Krombein, 1985 +) ( +Fig 42 +). + + + + \ No newline at end of file diff --git a/data/38/65/87/3865878FFF29C121FF75F987A19C5D90.xml b/data/38/65/87/3865878FFF29C121FF75F987A19C5D90.xml new file mode 100644 index 00000000000..2115b0a40aa --- /dev/null +++ b/data/38/65/87/3865878FFF29C121FF75F987A19C5D90.xml @@ -0,0 +1,374 @@ + + + +Additions to the knowledge of the Tribe Alyssontini (Hymenoptera: Crabronidae Bembicinae) in India with description of two new species of the genus Alysson Panzer + + + +Author + +Kumar, P. Girish +0000-0003-2121-0165 +Western Ghats Regional Centre, Zoological Survey of India, Eranhipalam, Kozhikode, Kerala- 673006, India. kpgiris @ gmail. com; https: // orcid. org / 0000 - 0003 - 2121 - 0165 +kpgiris@gmail.com + + + +Author + +Sheela, S. +Zoological Survey of India, M-Block, New Alipore, Kolkata, West Bengal- 700053, India. + + + +Author + +Sharma, Gaurav +0000-0003-2644-8797 +Northern Regional Centre, Zoological Survey of India, 218, Kaulagarh Road, Dehra Dun, Uttarakhand- 248195, India. drgaurav. sharma @ gov. in; https: // orcid. org / 0000 - 0003 - 2644 - 8797 +drgaurav.sharma@gov.in + +text + + +Zootaxa + + +2020 + +2020-10-16 + + +4861 + + +2 + + +270 +280 + + + +journal article +9026 +10.11646/zootaxa.4861.2.7 +af129ee5-c45e-4f33-bdfc-4c14402580e4 +1175-5326 +4416251 +C012766D-090F-491D-85CB-2A7BB388E885 + + + + + + + +Alysson himachalensis +Girish Kumar + +, +sp. nov. + + + + + + +( +Figs 11–20 +) + + + +urn:lsid:zoobank.org:act: +E6A6ACAF-D897-4C25-9AB5-FDF7DD6BD813 + + + + + +Type material. + +Holotype + +, + +India + +: + +Himachal Pradesh + +, +Chamba district +, +Catchment Ala +( +32° 31’ 28’’ N +& +76° 00’ 07’’ E +, + +2289 m + +), + +15.viii.1971 + +, +Coll. Sukh Dev +, +ZSIK +Regd. No. +ZSI/ +WGRC +/IR/INV.14403 + +. + +Paratype + +, +Chamba district +, +Dalhousie +( +32° 32’ 09’’ N +& +75° 58’ 46’’ E +, + +2133 m + +), + +21.viii.1972 + +, +Coll. Khan +, +ZSIK +Regd. No. +ZSI/ +WGRC +/ IR/INV.14404 + +. + +Paratype + +, +Chamba district +, +Dainkund Peak +( +32° 31’ 25’’ N +& +76° 01’ 37’’ E +, + +2723 m + +), + +30.vii.1971 + +, +Coll. Tulsi +, +ZSIK +Regd. No. +ZSI/ +WGRC +/IR/INV.14405 + +. + + + + +Diagnosis +. This new species differs from all other species of the genus by having the following combination + + +of characters: Gt +1 +completely and Gt +2 +mostly yellowish red (except black apex and typical creamy yellow lateral spots on second tergite); propodeal enclosure apically triangularly pointed, only longitudinally carinated inside; mesosoma (except tegulae brown) entirely black (with bluish reflections), without ferruginous red markings. This new species comes close to + +A. bengalensis + +sp. nov. +and + +A. triangularis +Krombein + +in having propodeal enclosure apically triangularly pointed, and mesosoma (except tegulae brown) entirely black, without ferruginous red markings but distinctly differs from both of them in having Gt +1 +completely and Gt +2 +mostly yellowish red (in + +A. bengalensis + +sp. nov. +and + +A. triangularis +Krombein + +, metasoma entirely black, except paired, rounded creamy white anterolateral spots on Gt +2 +). As per the key of +Nemkov (2014) +, the female of this new species comes close to a widely distributed Palearctic species + +A. spinosus +(Panzer, 1798) + +in general colour pattern especially having metasomal base red. But this new species clearly differs from + +A. spinosus + +by absence of creamy white spots on scutellum (in + +A. spinosus + +, distinct and large creamy white spots on scutellum present in both female and male) and reduced yellow markings on clypeus and towards lower half of inner eye margins (in + +A. spinosus + +, yellow markings on clypeus and inner eye margins are more prominent in both female and male). Not only the aforementioned differences, + +A. spinosus + +have also an U-shaped metapostnotum and it belongs to another species group. As per the key for Chinese species by +Wu & Zhou (1987) +, this new species comes close to + +A. caeruleus +Wu & Zhou + +and + +A. sichuanensis +Wu & Zhou + +but distinctly differs from both. This new species clearly differs from + +A. caeruleus + +in having Gt +1 +completely and Gt +2 +mostly yellowish red (in + +A. caeruleus + +metasoma entirely black). This new species in having no yellow spot between antennal sockets (in + +A. sichuanensis + +a yellow spot present between antennal sockets). + + + + +Description. +Holotype +female ( +Fig. 21–30 +). Length +9.42 mm +; forewing length +7.31 mm +. +Colour. +Black (with bluish reflections on mesosoma), the following parts yellowish red: first metasomal segment completely and second metasomal segment mostly (except black apex and typical creamy yellow lateral spots on second tergite). The following parts creamy white to whitish yellow: mandible except apex, a band at apical half clypeus, which emarginated at middle above (not extending towards lateral margins of clypeus), narrow stripe along inner eye margin and not extending halfway to anterior ocellus, scape beneath, fore coxae beneath, narrow streak anteriorly on fore tibia, all segments of fore tarsus and fore claws, and pair of round anterolateral spots on Gt +2 +. The following pale brown: fore tibia (except narrow whitish yellow streak anteriorly), mid and hind tarsal segments, and tegula. The following dark brown: mid and hind femora and tibia. Wings clear except forewing with two infumated bands; outer infumated band covers most of marginal cell, apical third of first submarginal cell, second and third submarginal cells, outer half of third discoidal cell, extending toward posterior margin of wing; inner infumated band covers basal half of first discoidal cell, second discoidal cell almost entirely except apex and apex of submedial cell. Vestiture silvery, subappressed; some longer suberect setae also present on mandible, clypeus, mesopleuron, coxae and femora beneath, sides of Gt +3-6 +and Gs +2-6 +; pygidial setae silvery. + +Head +. + +Head width 1.91 × interocular distance at antennal insertions and 1.76 × that at anterior ocellus ( +Fig 12 +); apical margin of clypeus ( +Fig 13 +) trilobate, tooth-like, middle lobe larger than lateral lobes; labrum short, about as wide as lobate section of clypeus and with subtruncate apical margin; front with shallow median groove evanescent towards anterior ocellus, with small punctures; OOL 2.50 × POL (in female +paratypes +OOL 2.72–2.91 × POL); POL 0.38 × ocellooccipital distance (in female +paratypes +POL 0.35–0.37 × ocellooccipital distance). Antenna as in +Figure 14 +, length of antennal segments as follows, scape: pedicel: fu +1 +: fu +2 +: fu +3 +: fu +4 +: fu +5 +: fu +6 +: fu +7 +: fu +8 +: fu +9 +: fu +10 += 16: 7: 16.25: 16.25: 13: 13: 12: 11: 10: 10: 10: 13. +Mesosoma +. Pronotum dorsally with small punctures, mostly separated by about the width of the diameter of a puncture, with a crenulate groove posteriorly (groove narrowed towards middle); lateral surface of pronotum with few strong oblique rugulae on upper half, lower half mostly glabrous anteriorly; mesoscutum with small subcontiguous punctures; mesopleuron with tiny punctures separated by more than the diameter of a puncture. Dorsal side of propodeum ( +Fig 16 +) with propodeal enclosure apically triangularly pointed, inner side of enclosure only longitudinally carinated inside, outer side of enclosure with radiating striae from outer margins of enclosure and rugoso-reticulations towards periphery, lateral tooth well developed; posterior side of propodeum smooth on either sides of its median carina. Forewing ( +Fig 17 +) with second recurrent vein joins with third submarginal cell. +Metasoma +. Gt +1 +and Gt +2 +almost impunctate except for sparse, scattered setae on sides ( +Fig 19 +); base of Gt +1 +with strong longitudinal cavities on either side, margined by strong carina. + + + + +Etymology +. The species epithet is derived from the state of collection of the species, + +Himachal Pradesh + +. + + + + +Distribution +. +India +: +Himachal Pradesh +( +Fig 41 +). + + + + \ No newline at end of file diff --git a/data/38/65/87/3865878FFF2BC124FF75FC72A6E55CA1.xml b/data/38/65/87/3865878FFF2BC124FF75FC72A6E55CA1.xml new file mode 100644 index 00000000000..3374c2df459 --- /dev/null +++ b/data/38/65/87/3865878FFF2BC124FF75FC72A6E55CA1.xml @@ -0,0 +1,253 @@ + + + +Additions to the knowledge of the Tribe Alyssontini (Hymenoptera: Crabronidae Bembicinae) in India with description of two new species of the genus Alysson Panzer + + + +Author + +Kumar, P. Girish +0000-0003-2121-0165 +Western Ghats Regional Centre, Zoological Survey of India, Eranhipalam, Kozhikode, Kerala- 673006, India. kpgiris @ gmail. com; https: // orcid. org / 0000 - 0003 - 2121 - 0165 +kpgiris@gmail.com + + + +Author + +Sheela, S. +Zoological Survey of India, M-Block, New Alipore, Kolkata, West Bengal- 700053, India. + + + +Author + +Sharma, Gaurav +0000-0003-2644-8797 +Northern Regional Centre, Zoological Survey of India, 218, Kaulagarh Road, Dehra Dun, Uttarakhand- 248195, India. drgaurav. sharma @ gov. in; https: // orcid. org / 0000 - 0003 - 2644 - 8797 +drgaurav.sharma@gov.in + +text + + +Zootaxa + + +2020 + +2020-10-16 + + +4861 + + +2 + + +270 +280 + + + +journal article +9026 +10.11646/zootaxa.4861.2.7 +af129ee5-c45e-4f33-bdfc-4c14402580e4 +1175-5326 +4416251 +C012766D-090F-491D-85CB-2A7BB388E885 + + + + + + +Key to the species of Indian subcontinent + +Alysson + +(modified from +Tsuneki, 1968 +) + + + + + + + +1. Mesosoma with ferruginous red markings.................................................................. 2 + + +- Mesosoma (except tegulae) entirely black (sometimes with creamy white spots at pronotum and scutellum).............. 3 + + + + + + +2. Propleuron striate in middle; propodeal enclosure with two central carinae united at apex; setae on frons and vertex silvery. + +. +India +: +Himachal Pradesh +................................................. + + +Alysson erythrothorax +Cameron, 1902 + + + + + + + +- + +Propleuron simply aciculate at base, not striate; propodeal enclosure with two central carinae not united at apex; setae on frons and vertex black. + +, + +. +Sri Lanka +............................................. + + +Alysson ruficollis +Cameron, 1902 + + + + + + + + +3. Propodeal enclosure apically triangular.................................................................... 4 + + +- Propodeal enclosure apically rounded..................................................................... 6 + + + + + +4. First metasomal segment completely and second metasomal segment mostly yellowish red (except black apex and typical creamy yellow lateral spots on second tergite). + + +. +India +: +Himachal Pradesh +.............. + + +Alysson himachalensis + +sp. nov + + +. + + + +- Metasoma entirely black................................................................................ 5 + + + + + + +5. Propodeal enclosure only longitudinally carinated; outer area of dorsal side of propodeum with only few radiating striae from outer margins of propodeal enclosure; posterior side of propodeum on each side of the median carina smooth; no creamy white spots on pronotum, scutellum and basal fourth of hind tibia; OOL 3–4 × POL in female; forewing with two infumated bands in female; pygidial setae silvery. + +. +India +: +West Bengal +.................................. + + +Alysson bengalensis + +sp. nov + + +. + + + + +- + +Propodeal enclosure rugoso-reticulated; outer area of dorsal side of propodeum with numerous areolets; posterior side of propodeum areolated; pair of creamy white spots present on pronotum, scutellum and basal fourth of hind tibia; OOL 1.55 × POL in female; forewing with a single infumated band in female; pygidial setae brownish. + +, + +. +Sri Lanka +; +India +: +Tamil Nadu +........................................................................ + + +Alysson triangularis +Krombein, 1985 + + + + + + + + + + +6. Posterior side of propodeum areolated; clypeus with extreme apex brownish black; forewing with a single infumated band (scutellum with two spots; mid and hind legs blackish and from coxae apically subannulately maculated with yellow). ‘ + +’ = + +. +India +: +Maharashtra +, +West Bengal +.............................................. + + +Alysson annulipes +Cameron, 1897 + + + + + + + +- + +Posterior side of propodeum on each side of the median carina smooth; clypeus with extreme apex not brownish black; forewing with two infumated bands (mid and hind legs black, with tarsi dark brown). + +. +India +: +Himachal Pradesh +.................................................................................. + + +Alysson testaceitarsis +Cameron, 1902 + + + + + + + + + \ No newline at end of file diff --git a/data/38/65/87/3865878FFF2BC126FF75F901A1DF5C29.xml b/data/38/65/87/3865878FFF2BC126FF75F901A1DF5C29.xml new file mode 100644 index 00000000000..cad0204fd8e --- /dev/null +++ b/data/38/65/87/3865878FFF2BC126FF75F901A1DF5C29.xml @@ -0,0 +1,302 @@ + + + +Additions to the knowledge of the Tribe Alyssontini (Hymenoptera: Crabronidae Bembicinae) in India with description of two new species of the genus Alysson Panzer + + + +Author + +Kumar, P. Girish +0000-0003-2121-0165 +Western Ghats Regional Centre, Zoological Survey of India, Eranhipalam, Kozhikode, Kerala- 673006, India. kpgiris @ gmail. com; https: // orcid. org / 0000 - 0003 - 2121 - 0165 +kpgiris@gmail.com + + + +Author + +Sheela, S. +Zoological Survey of India, M-Block, New Alipore, Kolkata, West Bengal- 700053, India. + + + +Author + +Sharma, Gaurav +0000-0003-2644-8797 +Northern Regional Centre, Zoological Survey of India, 218, Kaulagarh Road, Dehra Dun, Uttarakhand- 248195, India. drgaurav. sharma @ gov. in; https: // orcid. org / 0000 - 0003 - 2644 - 8797 +drgaurav.sharma@gov.in + +text + + +Zootaxa + + +2020 + +2020-10-16 + + +4861 + + +2 + + +270 +280 + + + +journal article +9026 +10.11646/zootaxa.4861.2.7 +af129ee5-c45e-4f33-bdfc-4c14402580e4 +1175-5326 +4416251 +C012766D-090F-491D-85CB-2A7BB388E885 + + + + + + + +Alysson bengalensis +Girish Kumar + +, +sp. nov. + + + + + + +( +Figs 1–10 +) + + + +urn:lsid:zoobank.org:act: +C9751D38-2B8D-427B-9EBF-ABEE2A48C0C7 + + + + + +Type material. + +Holotype + +, + +India + +: + +West Bengal + +, +Kalimpong district +, +Neora Valley National Park +( +27° 04’ 56’’ N +& +88° 42’ 02’’ E +, + +2189 m + +), + +6.x.2018 + +, +Coll. S. Sheela +, +ZSIK +Regd. No. +ZSI/ +WGRC +/IR/INV.14401 + +. + +Paratype + +, same collection data of +holotype +, +ZSIK +Regd. No. +ZSI/ +WGRC +/IR/INV.14402 + +. + + + + +FIGURES 1–10. + +Alysson bengalensis + + +sp. nov. + +Holotype ♀. 1. Habitus, lateral view. 2. Head, frontal view. 3. Lower half of head, frontal view. 4. Antenna. 5. Head and mesosoma, dorsal view. 6. Propodeum, dorsal view. 7. Forewing. 8. Hindwing. 9. Metasoma, dorsal view. 10. Last metasomal tergite. + + + + +Diagnosis +. This new species differs from all other species of the genus by the following combination of characters: Metasoma entirely black; propodeal enclosure apically triangular, only longitudinally carinated inside; mesosoma (except tegula brownish on outer side) entirely black, without ferruginous red markings. This new species come close to + +A. triangularis +Krombein + +in having metasoma entirely black, propodeal enclosure apically triangularly pointed, and mesosoma (except tegulae brownish on outer side) entirely black, without ferruginous red markings but distinctly differs from + +A. triangularis + +in having the characters mentioned in the couplet number 5 of the key. As per the key for Chinese species by +Wu & Zhou (1987) +, this new species comes close to + +A. sichuanensis +Wu & Zhou + +and + +A. carinatus +Wu & Zhou + +but differs distinctly from both. It differs from + +A. sichuanensis + +in having no creamy white to yellow spot between antennal sockets (in + +A. sichuanensis + +a yellow spot present between antennal sockets) and clypeus with a creamy white to yellow band at apical half only (in + +A. sichuanensis + +most part of clypeus yellow except its basal margin and centre black). It differs from + +A. carinatus + +in having clypeus with a creamy white to yellow band at apical half (in + +A. carinatus + +, clypeus with two yellow spots) and second recurrent vein joining to third submarginal cell (in + +A. carinatus + +, second recurrent vein joining to second submarginal cell). + + + + +Description. +Holotype +female ( +Fig. 1–10 +). Length +7.83 mm +; forewing length +6.43 mm +. +Colour. +Black, the following parts creamy white: mandible except apex, a band at apical half of clypeus (not extending towards lateral margins of clypeus), narrow stripe along inner eye margin and extending halfway to anterior ocellus, scape beneath, fore coxa beneath, narrow streak anteriorly on fore tibia, and pair of round anterolateral spots on Gt +2 +. The following brown: tarsal segments, and outer sides of tegula. Wings clear except forewing with two infumated bands; outer infumated band covers most of marginal cell, apical third of first submarginal cell, second and third submarginal cells, outer half of third discoidal cell, extending toward posterior margin of wing; inner infumated band covers basal half of first discoidal cell, second discoidal cell almost entirely except apex and apex of submedial cell. Vestiture silvery, subappressed; some longer suberect setae also present on mandible, clypeus, mesopleuron, coxae and femora beneath, sides of Gt +3-6 +and Gs +2-6 +; pygidial setae silvery. + +Head +. + +Head width 1.98 × interocular distance at antennal insertions and 1.48 × that at anterior ocellus ( +Fig 2 +); apical margin of clypeus ( +Fig 3 +) trilobate, middle lobe larger than lateral lobes; labrum short, about as wide as lobate section of clypeus and with subtruncate apical margin; front with shallow median groove evanescent at upper half of front, with small punctures; OOL 3 × POL (in female +paratype +OOL 4 × POL); POL 0.36 × ocellooccipital distance. Antenna as in +Figure 4 +, length of antennal segments as follows, scape: pedicel: fu +1 +: fu +2 +: fu +3 +: fu +4 +: fu +5 +: fu +6 +: fu +7 +: fu +8 +: fu +9 +: fu +10 += 13: 7.7: 14: 13.5: 12.5: 11: 10: 10: 9.5: 9.5: 9: 12.5. +Mesosoma +. Pronotum dorsally with small punctures, mostly separated by about the width of the diameter of a puncture, with a crenulate groove posteriorly (groove narrowed towards middle); lateral surface of pronotum with some strong oblique rugulae on upper half, lower half mostly glabrous anteriorly; mesoscutum with small subcontiguous punctures; mesopleuron with tiny punctures separated by several times the diameter of a puncture. Dorsal side of propodeum ( +Fig 6 +) with propodeal enclosure apically triangularly pointed, inner side of enclosure only longitudinally carinated, outer side of enclosure with radiating striae from outer margins of enclosure and few rugoso-reticulations towards periphery, lateral tooth well developed; posterior side of propodeum smooth on either sides of its median carina. Forewing ( +Fig. 7 +) with second recurrent vein joins with third submarginal cell. + + +Metasoma +. Gt +1 +and Gt +2 +almost impunctate except for sparse, scattered setae on sides ( +Fig 9 +); base of Gt +1 +with strong longitudinal cavities on either side, margined by strong carina. + + + + +Etymology +. The species epithet is derived from the state of collection of the species, + +West Bengal + +. + + + + +Distribution +. +India +: +West Bengal +( +Fig 41 +). + + + + \ No newline at end of file diff --git a/data/38/65/B6/3865B6981165DB4F11537A56D5BDD154.xml b/data/38/65/B6/3865B6981165DB4F11537A56D5BDD154.xml new file mode 100644 index 00000000000..99b7b662bdb --- /dev/null +++ b/data/38/65/B6/3865B6981165DB4F11537A56D5BDD154.xml @@ -0,0 +1,74 @@ + + + +Species plantarum: exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas + + + +Author + +Linnaeus, Carolus + +text + +1753 +Laurentius Salvius + +Stockholm + + + +https://doi.org/10.5962/bhl.title.669 + +book +10.5281/zenodo.3931989 +3931989 + + + + + +Androsace +septentrionalis + +, +spec. nov. + + + + +2. Androsace foliis lanceolatis dentatis glabris, perianthiis angulatis corolla brevioribus. +Fl. suec. 160. + + +Androsace calyce fructus parvo. +Fl. lapp.78. + + +Androsace montana, flore minore. +Buxb. act. 2. p.369. t.23. f.2. + + +Alsine verna, androsaces capitulis. +Bauh. pin. 251. prod. 118. + + +Alsine minor, androsaces alterius racie. +Bauh. pin. 251. prodr. 118. + + +Alsine adfinis Androsace dicta minor. +Bauh. pin. 251. + + + + +Habitat in alpibus +Lapponiae +, +Russiae +apricis glareosis. ☉ + + + + \ No newline at end of file diff --git a/data/38/65/BA/3865BAABD96631B6F5126DC9EBD9878E.xml b/data/38/65/BA/3865BAABD96631B6F5126DC9EBD9878E.xml new file mode 100644 index 00000000000..4a3106414b3 --- /dev/null +++ b/data/38/65/BA/3865BAABD96631B6F5126DC9EBD9878E.xml @@ -0,0 +1,66 @@ + + + +Ameisen aus Rhodesia, Kapland usw. (Hym.) Gesammelt von Herrn G. Arnold, Dr. H. Brauns und anderen. + + + +Author + +Forel, A. + +text + + +Deutsche Entomologische Zeitschrift + + +1913 + +1913 + + +203 +225 + + + + +http://antbase.org/ants/publications/4059/4059.pdf + +journal article +4059 +501AECAA-BC7F-4DE8-8A8C-90FED0E21463 + + + + +Leptogenys Ferrarii +n. sp. + + + + +[[ worker ]]. L.: 4,7 mm. Kiefer glatt, glaenzend, zerstreut punktiert, erheblich kuerzer als der Kopf, ziemlich gerade, nur am letzten Drittel schwach konvex, gegen die Spitze zu schwach, aber merklich etwas verbreitert, ohne Spur von Zahn (ausser dem Endzahn), und auch ohne Spur von Endrand .. Diese Kiefer stellen unsere Art unbedingt zu +Leptogenys +sens. strict., waehrend sie sonst der +Leptogenys (Lobopelta) nitida +Sm. sehr nahe steht, sowie auch der +castanea Mayr +. Clypeus sehr stark gekielt, mit einfach dreieckigem Vorderlappen. Kopf rechteckig, deutlich laenger als breit, vorn etwas breiter als hinten, mit schwach konvexem Hinterrand und auch schwach konvexen Seiten. Augen mittelgross, am vorderen Drittel. Fuehlerschaft den Hinterrand sehr wenig ueberragend. Geisselglieder 7 — 9 ungefaehr so dick wie lang, alle anderen laenger als dick. ' Thorax wie bei +Lobopelta nitida +. Basalflaeche des Epinotums, gut doppelt so lang wie die abschuessige, und von ihr etwas deutlicher abgeschieden. Knoten kubisch, hinten und vorn senkrecht gestutzt, etwas mehr als 1 1 / 2 mal hoeher als lang. Seine obere Flaeche ist fast gerade, scharf von der Hinter- und Vorderflaeche abgeschieden, obwohl hinten und vor allem vorn nicht gerandet, von hinten nach vorn sehr schwach, aber sichtbar absteigend. Der ganze Knoten von oben gesehen ist hinten eher etwas breiter als lang, und hinten deutlich breiter als vorn. Hinterleib eher schwach eingeschnuert. Beine maessig lang. Die Hinterflaeche des Knotens ist flach und seitlich recht stumpf gerandet. + +Glaenzend und ziemlich glatt. Kopf sehr fein und ziemlich weitlaeufig punktiert. Pronotum mit groeberen, weitlaeufigen Punkten, seitlich mit laenglichen Gruebchen; Schuppe, Mesonotum und Epinotum mit aehnlicher Skulptur, aber die abschuessige Flaeche des Epinotums ist quer gestreift. Am Hinterleib nur sehr schwache haartragende Punkte. Koerper und Glieder sehr kurz, hellgelblich, und nicht reichlich abstehend behaart; diese Haare sind an der Schuppe und am Hinterleib etwas laenger und an den Gliedern etwas schief. Braeunlichschwarz; Kiefer, Clypeus, Fuehler, Beine und Spitze des Hinterleibs roetlich. + + + +Bulawayo, Rhodesia, im Garten des Herrn Arnold. Diese Art zeigt deutlich, wie nahe die Untergattungen +Leptogenys +und +Lobopelta +einander stehen. + + + + \ No newline at end of file diff --git a/data/38/66/2C/38662C25B1E580B7E9AFB807DCFA90B7.xml b/data/38/66/2C/38662C25B1E580B7E9AFB807DCFA90B7.xml new file mode 100644 index 00000000000..e4558fdfede --- /dev/null +++ b/data/38/66/2C/38662C25B1E580B7E9AFB807DCFA90B7.xml @@ -0,0 +1,147 @@ + + + +Flora Helvetica - Salicaceae + + + +Author + +Konrad Lauber + + + +Author + +Gerhart Wagner + + + +Author + +Andreas Gygax + +text + + +2018 +Haupt Verlag + +Bern + + + +Flora Helvetica + + + +428 +446 + + + +book chapter +978-3-258-08047-5 + + + + + + +Populus +x +canadensis + +Moench + + + + + +Artbeschreibung: Hybride + +P. nigra + +x +deltoides +, wie + +P. nigra + +, aber Stamm nicht wulstig, junge Triebe mit Korkrippen. +Blaetter +8-12 cm +lang, anfangs locker bewimpert, an der Basis meist mit 1-2 +Druesen +. Narben 3-4. + + + + +Bluetezeit +: 4 + + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F--Lichtzahl L--Salzzeichen--
Reaktionszahl R--Temperaturzahl T--
+Naehrstoffzahl +N +-- +Kontinentalitaetszahl +K +--
+
+
+ + +Volksname Deutscher Name: +Kanadische Pappel +Nom +francais +: +Peuplier du Canada +Nome italiano: + +Pioppo del +Canada + + + +
+
\ No newline at end of file diff --git a/data/38/66/63/38666349B7F95837B729D4B6F0183C5E.xml b/data/38/66/63/38666349B7F95837B729D4B6F0183C5E.xml new file mode 100644 index 00000000000..586f39ee01f --- /dev/null +++ b/data/38/66/63/38666349B7F95837B729D4B6F0183C5E.xml @@ -0,0 +1,101 @@ + + + +The medicinal plants of Myanmar + + + +Author + +DeFilipps, Robert A. +Deceased + + + +Author + +Krupnick, Gary A. +https://orcid.org/0000-0002-1357-4826 +Department of Botany, National Museum of Natural History, Smithsonian Institution, PO Box 37012, MRC- 166, Washington, DC, 20013 - 7012, USA +krupnick@si.edu + +text + + +PhytoKeys + + +2018 + +2018-06-28 + + +102 + + +1 +341 + + + + +http://dx.doi.org/10.3897/phytokeys.102.24380 + +journal article +http://dx.doi.org/10.3897/phytokeys.102.24380 +1314-2003-102-1 +AA226A35FFF8FFBC37621A40C2518C67 +1306325 + + + + +Artabotrys hexapetalus (L.f.) Bhandari (= Artabotrys odoratissimus R.Br.) + + + +Names. + +Myanmar +: +kadat-ngan +, +padat-nygan +, +tadaing-hmwe +. +English +: climbing ylang-ylang. + + + +Range. +Sri Lanka and southern India; cultivated widely in the tropics. Widely distributed in Myanmar. + + +Use. + +Leaf +: Used in cholera. ( +Flower +: Used in perfumery). + + + +Notes. +As a Chinese folk medicine, its root and fruit are used to treat malaria and scrofula. + +Leaf extracts of this species are used for antifertility; flowers for a stimulating tea-like beverage and also to extact essential oil used in perfume. Fruits are eaten by indigenous people to maintain their health. Additional medicinal uses of this species include as an antifungal, cardiac depressor, for cholera, and as a hypotensive and weak estrogenic ( +Manjula et al. 2011 +). + + + +Reference. + +Nordal (1963) +. + + + + \ No newline at end of file diff --git a/data/38/66/87/386687B40F67336E4983957EFC637BAD.xml b/data/38/66/87/386687B40F67336E4983957EFC637BAD.xml new file mode 100644 index 00000000000..ca19a571f33 --- /dev/null +++ b/data/38/66/87/386687B40F67336E4983957EFC637BAD.xml @@ -0,0 +1,1387 @@ + + + +Morphological variation of the Long-tailed Reed Finch Donacospiza albifrons (Vieillot, 1817) (Aves: Thraupidae) + + + +Author + +Lopes, Leonardo Esteves + +text + + +Zootaxa + + +2017 + +2017-10-05 + + +4329 + + +3 + + +201 +218 + + + +journal article +31896 +10.11646/zootaxa.4329.3.1 +b70d435f-a3a7-4a26-9be7-0cc4908a91e9 +1175-5326 +1002432 +A1Fa25B9-E28F-407A-B1Ec-4E78A952E472 + + + + + + + +Introduction + + + + + + +The Long-tailed Reed Finch + +Donacospiza albifrons +( +Vieillot, 1817 +) + +is a patchily distributed species found in reed beds, damp grasslands, and scrubs, usually near water, ranging from southeastern +Brazil +to +Uruguay +, northeastern +Argentina +and + +Paraguay + +( + +Parker +et al. +1996 + +; +Ridgely & Tudor 2009 +; +Jaramillo 2011 +). An allopatric population is found in the seasonally wet grasslands of +Bolivia +( +Schimitt & Schimitt 1987 +; +Brace & Hornbuckle 1998 +; + +Maillard +et al. +2008 + +; +Lane 2014 +), isolated by almost +1,000 km +of intervening dry habitats. + + + + +The species is rare in collections and few institutions harbor series larger than +10 specimens +, always with limited geographical coverage. Consequently, the large morphological variation observed in the species has been attributed, to a variable extent, to age and/or sex by previous authors, with considerable disagreement. Some authors describe females as slightly paler below and more striated above ( +Sharpe 1888 +; +Hellmayr 1938 +; Meyer de +Schauensee 1970 +; +Armani 1985 +; +Dunning 1987 +; +Ridgely & Tudor 1989 +; +Perlo 2009 +). +Jaramillo (2011) +states that the “female is very like male, perhaps slightly less colourful, but much overlap in appearance.” Some other authors consider that sexual dichromatism does not exist and attribute morphological variation exclusively to age ( +Narosky & Yzurieta 2003 +; +Willis & Oniki 2003 +; +Grantsau 2010 +; +Azpiroz 2012 +) and feather wear, with the cinnamon-buff underparts becoming whitish in specimens with very abraded plumage ( +Azpiroz 2012 +). No author has ever reported geographic variation in the species, although +Lane (2014) +, after comparing specimens from +Bolivia +and southeastern +Brazil +, suggested that the taxonomy of the species should be investigated. + + +While collecting birds in the Espinhaço Range, southeastern +Brazil +, I obtained Long-tailed Reed Finch specimens that were much paler and less streaked on the upperparts than depicted in popular field guides (e.g. +Ridgely & Tudor 2009 +). These birds were collected in dry grasslands at high elevations (ca. +1500 m +asl), a habitat quite distinct from that previously reported for the species, which is usually found near water and at lower elevations. Initially, I suspected I had collected an undescribed species, especially because the Espinhaço Range is a well-known center of bird endemism ( + +Stattersfield +et al. +1998 + +; + +Vasconcelos +et al. +2008 + +) from where new species have recently been described ( +Vielliard 1990 +; + +Gonzaga +et al. +2007 + +; + +Whitney +et al. +2010 + +; + +Freitas +et al. +2012 + +). + +Nevertheless, after collecting additional specimens and analyzing the largest series of Long-tailed Reed Finches in any study, I found that my initial hypothesis was incorrect. Here I present a detailed study of the morphological variation in the species, including its plumage sequence and a revision of its taxonomy. Before proceeding, a brief review of the taxonomic history of the species is presented. + +Taxonomic and nomenclatural history. + +Sylvia albifrons +Vieillot, 1817 + +, is based on “Cola Aguda del Vientre de Canela”, bird number CXXXIV of +Azara (1805) +, who observed the species in + +Paraguay + +. +Vieillot (1817) +did not clearly state whether he had examined any specimens, but he probably based the description exclusively on the writings of +Azara (1805) +. + + +Systematic relationships of the species have long been disputed. The monospecific genus + +Donacospiza +Cabanis + +was erected for the bird described by Vieillot ( + +Cabanis & Heine +1850 + +–1851), but the species has also been placed in the genus + +Poospiza +Cabanis + +by +Sclater (1864) +, + +Emberizoides +Temminck + +by +Gray (1870) +, and + +Coryphaspiza +G. R. Gray + +by +Sharpe (1888) +. + + +The species has been traditionally placed among the emberizid passerines (e.g. +Sharpe 1888 +; +Hellmayr 1938 +; +Paynter & Mayr 1970 +), but recent molecular studies showed that + +Donacospiza + +is best placed among the +Thraupidae +, embedded within the subfamily Poospizinae, in a clade containing + +Cypsnagra +Lesson + +and + +Poospizopsis +von Berlepsch + +( + +Lougheed +et al. +2000 + +; +Shultz & Burns 2012 +; + +Barker +et al. +2013a + +; + +Burns +et al. +2014 + +, +2016 +). Strong reciprocal response to cross playback of + +D. albifrons + +has been observed for the Cinereous Warbling Finch + +Microspingus cinereus +(Bonaparte) ( +Ribon 2002 +) + +and the Black-and-rufous Warbling Finch + +Poospiza nigrorufa +(d’Orbigny & Lafresnaye) ( +Rising 2011 +) + +, providing additional evidence of the close relationship between these genera. + +The Long-tailed Reed Finch includes as junior synonyms two other names, which are discussed below. + + +Ammodramus longicaudatus +Gould, 1839 + +, was described from birds collected by Charles Darwin during his voyage aboard the H.M.S. Beagle (Darwin +1838–1841 +; +Steinheimer 2004 +; + +Steinheimer +et al. +2006 + +). This name was based on an unspecified number of +syntypes +collected in +Montevideo +and +Maldonado +, +Uruguay +(Darwin +1838– 1841 +). +Sharpe (1888) +cited two “adult” birds collected by Darwin and deposited in the Natural History Museum, specimen “h” from +Maldonado +and specimen “i” from +Montevideo +, referring this last specimen as the +type +of this name. +Warren (1971) +and +Steinheimer (2004) +considered both specimens as +syntypes +. + + + +Poospiza oxyrhyncha +Sclater, 1864 + +, was described from a female obtained in exchange with the “ +Vienna +Museum”. The +type +locality is Curitiba, state of +Paraná +, southern +Brazil +( +Sclater 1864 +) and the +holotype +is housed in the Natural History Museum ( +Warren & Harrison 1971 +). +Sclater (1869) +soon recognized that the name proposed by him was a junior subjective synonym of that proposed by +Vieillot (1817) +. + + + + + + + +Material and methods + + + +During the last ten years, I conducted limited fieldwork in the state of +Minas Gerais +, southeastern +Brazil +, searching for the Long-tailed Reed Finch. I collected specimens with mist-nets and air rifles and took notes on habitat. + + +The taxonomic and morphological analyses conducted here were based on plumage coloration and morphometric characters of +141 specimens +(Appendix 1, +Figure 1 +) housed in 18 ornithological collections: Academy of Natural Sciences of Philadelphia, Philadelphia, +USA +( +ANSP +); American Museum of Natural History, + +New +York + +, +USA +( +AMNH +); Carnegie Museum of Natural History, Pittsburgh, +USA +(CM); +Centro +de Coleções Taxonômicas da Universidade Federal de +Minas Gerais +, Belo Horizonte, +Brazil +(DZUFMG); Field Museum, Chicago, +USA +( +FMNH +); +Louisiana +State University Museum of Natural Science, Baton Rouge, +USA +( +LSUMZ +); Museu de Ciências Naturais da Pontifícia Universidade Católica de +Minas Gerais +, Belo Horizonte, +Brazil +( +MCNA +); Muséum National D’Histoire Naturelle, Paris, +France +( +MNHN +); Museu Nacional, +Rio de Janeiro +, +Brazil +( +MNRJ +); Museu Paraense Emílio Goeldi, Belém, +Brazil +( +MPEG +); Museu de Zoologia João Moojen da Universidade Federal de Viçosa, Viçosa, +Brazil +( +MZJMO +); Museu de Zoologia da Universidade de +São Paulo +, +São Paulo +, +Brazil +( +MZUSP +); Natural History Museum, Tring, +UK +( +NHMUK +; formerly +BMNH +); Naturhistorisches Museum, +Vienna +, +Austria +( +NMW +); Naturhistoriska Riksmuseet, +Stockholm +, +Sweden +( +NRM +); Senckenberg Naturmuseum, Frankfurt, +Germany +( +SMF +); National Museum of Natural History, +Washington +, DC, +USA +( +USNM +); and Museum für Naturkunde, +Berlin +, +Germany +( +ZMB +). + + + +FIGURE 1 +. Map showing the collection sites of the specimens of the Long-tailed Reed Finch + +Donacospiza albifrons + +examined in this study. The dashed line indicates the range of the species according to BirdLife International & Handbook of the Birds of the World (2016). + + + +I examined the +holotype +of + +Poospiza oxyrhyncha +Sclater, 1864 + +( +NHMUK +1885.2.10.314), and one +syntype +of + +Ammodramus longicaudatus +Gould, 1839 + +( +NHMUK +1856.3.15.9). The other +syntype +of + +A. longicaudatus + +( +NHMUK +1856.3.15.13) was not found. The +type +of + +Sylvia albifrons +Vieillot, 1817 + +, was not found in any of the collections visited and I failed to trace its location. I believe that this +type +, if once preserved, is lost, as is the rule for birds described by Vieillot from the works of Azara ( +Lopes & Gonzaga 2016a +). Geographical coordinates were obtained directly from the original sources or from ornithological gazetteers ( +Paynter 1989 +, +1992 +, +1995 +; +Paynter & Traylor 1991 +; +Vanzolini 1992 +). + + + + +The first step in the interpretation of color variation in the Long-tailed Reed Finch was to identify its plumage sequence and molting patterns, for which I followed the +Humphrey & Parkes (1959) +system. To determine the approximate schedule of breeding and molting in the species, for which no previous study was available, I conducted a thorough literature review and checked for gonadal data on labels of museum specimens. Given that the species lives in an abrasive habitat and feather wear results in significant changes in plumage color ( +Azpiroz 2012 +), I classified the plumage of each specimen accordingly to its stage of overall feather abrasion (Rogers 1 990): new, slightly abraded, abraded, and very abrade. This simple classification aided evaluation of the impact of feather abrasion upon plumage coloration. I used a color catalogue ( +Munsell Color 2000 +) as an aid for plumage comparisons and a dial caliper for measuring to the nearest +0.1 mm +the length (mm) of total culmen, closed wing (chord), tail, and tarsus ( + +Baldwin +et al. +1931 + +). + + +Delimitation of groups. +Given the large color and morphometric variation observed in the Long-tailed Reed Finch, as well as the lack of previous taxonomic hypotheses regarding it, I tentatively used three approaches to delimit groups within the taxon. First, I attempted several clustering techniques ( +e.g. +UPGMA with Euclidian Distances; +Tabachnick & Fidell 2007 +) to identify naturally occurring groups based on body size alone, without delimiting them +a priori +. This technique was ineffective, because birds collected in the same or in very close localities appeared scattered throughout the dendrogram, with no consistent trend (data not shown). Second, I attempted to delimit groups based on plumage coloration alone, but as discussed below, I was unable to delimit clear-cut boundaries between populations. Third, I divided the examined specimens into five groups based on geographic and habitat features, roughly following the limits, but not the names, of those biogeographical provinces recognized by +Morrone (2014) +: 1) RP—Río de la Plata (lowlands below +400 m +in + +Paraguay + +, +Argentina +, +Uruguay +, and the Brazilian state of +Rio Grande do Sul +); 2) SB—Southern +Brazil +(uplands between +700–1200 m +in the states of +Rio Grande do Sul +, +Santa Catarina +, and +Paraná +); 3) SU—Southeastern +Brazil +Uplands (areas between +400–800 m +in the states of +São Paulo +and +Rio de Janeiro +); 4) SH—Southeastern +Brazil +Highlands (above +1200 m +in the states of +Minas Gerais +, +Rio de Janeiro +, and +Espírito Santo +); and 5) LM—Llanos de Moxos (lowlands below +200 m +in +Bolivia +). Groups delimited in this third approach were used in the following statistical analyses, which only considered specimens in definitive basic plumage (see below). + + +Statistical analyses. +Differences between mean measurements of males and females were tested with the Student's t-test ( +Zar 2010 +). Given that preliminary analyses revealed that the species shows geographic variation in body size (see below), this test was performed only with specimens from the Río de la Plata, the only region from where samples were large enough for testing. Given the small sample sizes and the large standard deviations of some groups, I did not conduct statistical comparisons between mean measurements of them, because investigating diagnosability is more important than simply pointing out mean differences between populations ( +Patten & Unitt 2002 +). Therefore, I present box plot comparisons between body measurements of the five groups identified here and assessed their diagnosability using the method proposed by +Patten & Unitt (2002) +. I also conducted a principal component analysis (PCA) with varimax rotation using the following variables: length of total culmen, closed wing, tail, and tarsus ( +Tabachnick & Fidell 2007 +). + + +I investigated the hypothesis of clinal variation in body size with respect to Bergmann’s Rule ( +Rensch 1938 +; +James 1970 +), the tendency of organisms to be smaller in warmer areas and larger in colder areas ( +Zink & Remsen 1986 +; + +Blackburn +et al. +1999 + +; +Meiri 2011 +). I tested this hypothesis with the Spearman's correlation coefficient ( +Zar 2010 +) comparing body size (measured as the first principal component scores, +Zink & Remsen 1986 +) and average mean annual temperature at each collection site. For this analyses I conducted a second PCA with the same morphometric variables, but extracted only one component. Data from mean annual temperature (current conditions ~1960–1990) were obtained from WorldClim 1.4 with a spatial resolution of 30 seconds ( + +Hijmans +et al. +2005 + +). All analyses were performed using STATISTICA 8.0 software ( +StatSoft 2007 +), with a significance level of 5%. + + + + + + +Results + + + + +The Long-tailed Reed Finch is locally distributed in +Minas Gerais +. I met with it in five localities in the Southeastern +Brazil +Highlands, all of them in the southern portion of the Espinhaço Range: Parque Nacional da Serra do Cipó, Morro do Pilar ( +19°16’S +, +43°31’W +, +1250–1350 m +), Parque Estadual do Rola Mola, Brumadinho ( +20°03’S +, +44°00’W +, +1400–1500 m +), Retiro das Pedras, Nova Lima ( +20°05’S +, +44°00’W +, +1300 m +), Saramenha, Ouro Preto ( +20°24’S +, +43°33’W +, +1300–1400 m +), and Parque Estadual do Itacolomi, Ouro Preto ( +20°25’S +, +43°30’W +, +1300–1550 m +). In all these localities, the Long-tailed Reed Finch was found in mountainous areas with steep slopes covered by dry open grasslands with few shrubs and trees, usually with rock outcrops and always far from water ( +Figure 2 +). I collected eight specimens that were deposited in DZUFMG (see below), which represent the first specimens obtained in the central portion of +Minas Gerais +. + + + + +Breeding season. +Males with enlarged testes were collected in Sep (SH—DZUFMG 7164, 7165; RP—USNM 630463), Oct (LM—LSUMZ 124921, 124922) and Jan (SH—DZUFMG 4895). A female collected on +8 Nov 1979 +presented a well-developed egg in its oviduct (SU—MPEG 33275). Specimens collected in Jun–Aug presented small gonads. Therefore, breeding season of this species extends from at least Sep–Jan. + + + + +FIGURE 2. +Typical habitat of the Long-tailed Reed Finch + +Donacospiza albifrons + +at the northern portion of its range (Southeastern Brazil Highlands), in the Parque Estadual do Rola Moça, municipality of Brumadinho, Minas Gerais, Brazil (20°03’33’’S, 44°00’26’’W, 1400 m asl). The species inhabits the drier and higher areas of the park. + + + + +Plumage sequence, feather abrasion, and molts. +I detected no sexual dichromatism in the Long-tailed Reed Finch, and the large variation in color can be attributed, to a variable extent, to age, plumage condition, and geography. I identified three distinct and well-marked plumages in the species: juvenal, first basic, and definitive basic ( +Figure 3 +). The Long-tailed Reed Finch does not exhibit an alternate plumage. + + +Juveniles were collected in Nov (RP—USNM 55789, with abraded plumage), Dec (SB—AMNH 315995, with abraded plumage; SU—AMNH 315990 and 315994, with severely abraded plumage; RP—AMNH 388282 and 388283, with severely abraded plumage), and Feb (SU—MZUSP 355, with slight abraded plumage). All but one specimen collected in Nov and another in Dec were molting to a variable extent into the first basic plumage. Therefore, Long-tailed Reed Finches seem to retain the juvenal plumage for about two months after fledging. An additional specimen in the juvenal plumage (RP—NHMUK 1897.11.14.35, slightly abraded) was collected on +29 Jun +in +Argentina +. + +Birds in first basic plumage, but showing a few remaining juvenal contour feathers scattered throughout the body (i.e. finishing the first prebasic molt), were collected in Oct (LM—LSUMZ 124924, 124926), Jan (SH— DZUFMG 4897), Feb (SU—LSUMZ 68294), and Mar (SH—MNRJ 27697). Birds in first basic plumage were collected in Feb (RP—AMNH 813075), Mar (SB—MZUSP 38907), Apr (SB—MNRJ 37640), Jun (RP— NHMUK 1856.3.15.9), Aug (RP—AMNH 519698 and ZMB 2000/27004), Oct (LM—LSUMZ 124920), and Nov (RP—AMNH 519693). Therefore, first basic plumage is retained for at least six months. + +Body feathers of definitive plumaged birds are generally new from Mar onwards, with first signs of wear on Jul–Aug. Plumage becomes progressively worn until reaching a very abraded state in Feb and early Mar ( +Figure 3 +), when molt begins. Therefore, molt seems to occur just after the breeding season. A similar molting pattern seems to occur throughout the range of the species. + + +Plumage appearance. +The three plumages of topotypical specimens (i.e., those from + +Paraguay + +, the +type +locality of the species, or nearby along the Río de la Plata) with new plumage are described below. I also present comments on variation in plumage coloration caused by feather abrasion ( +Figure 3 +) and geography ( +Figures 4 +and +5 +). + + +Juvenal plumage: +Birds in this plumage are identifiable by their fluffy appearance, predominantly pale yellow throughout, and heavily streaked upperparts, breast, and sides. Crown, nape, interscapulars, and rump feathers very dark brown (10YR 2/2) edged ( +1–2mm +) pale yellow (2.5Y 8/4), resulting in a heavily streaked appearance; underparts (chin, throat, breast and belly) pale yellow (2.5Y 8/3), with the feathers of the breast and sides presenting the central shafts very dark grayish brown (10YR 3/2); lores and indistinct supercilium pale yellow (2.5Y 8/4); auriculars grayish brown (2.5Y 5/2); primaries and secondaries very dark grayish brown (10YR 3/2) edged dark grayish brown (2.5Y 4/2) on the outer vanes; greater and marginal wing coverts, as well as tertials, very dark grayish brown (10YR 3/2) edged pale yellow (2.5Y 7/4); rectrices very dark grayish brown (10YR 3/2) edged dark grayish brown (2.5Y 6/4) on the outer vanes; under wing coverts pale yellow. +Individual, wear, and geographic variation: +difficult to appreciate, given that only a few specimens, several of them molting to the first basic, were available for examination. Furthermore, specimens in juvenal plumage were available from only three of the five groups delimited here, with no specimens from Southeastern +Brazil +Highlands and Llanos de Moxos. + + +First basic plumage: +Birds in this plumage are identifiable by their lighter and brownish crown, their yellowish supercilium, and more heavily streaked upperparts. Feathers of the crown and nape light olive brown (2.5Y 5/4) with the central shafts black (2.5Y 2.5/1), resulting in a streaked appearance; interscapulars brownish yellow (10YR 6/8) with the central shafts black (2.5Y 2.5/1); rump brownish yellow (10YR 6/8); upper tail coverts yellowish brown (10YR 5/6) with the central shafts black; chin and throat yellow (10YR 8/6); breast yellow (10YR 7/6), with the feathers presenting a small spot very dark grayish brown (10YR 3/2) in the central shaft, resulting in a spotted appearance; belly and sides yellow (10YR 7/6), with the central shafts of side feathers very dark grayish brown (10YR 3/2), resulting in a streaked appearance; supercilium and lores yellow (2.5Y 8/6); auriculars light yellowish brown (2.5Y 6/4); primaries and secondaries very dark brown (10YR 2/2) edged pale yellow (10YR 6/4) on the outer vane; greater wing coverts and tertials very dark brown (10YR 2/2) edged yellowish brown (10YR 5/ 8) on the outer vanes; marginal wing coverts gray (5Y 5/1); rectrices very dark brown (10YR 2/2) edged light yellowish brown (2.5Y 6/4) on the outer vanes; under wing coverts whitish. +Individual and wear variation: +difficult to appreciate given the small number of specimens available. +Geographic variation: +marked, even though the scarce material available precludes a thorough evaluation of it. Birds from the northern range (Southeastern +Brazil +Highlands) are much paler throughout and with a greenish cast on the upperparts. Main differences are: feathers of crown and nape olive (5Y 5/3) with the central shafts black, resulting in a streaked appearance; interscapulars light olive brown (2.5Y 5/3) with the central shafts black; rump light olive brown (2.5Y 5/4); upper tail coverts olive brown (2.5Y 4/3); chin pale yellow (2.5Y 8/3); throat pale yellow (2.5Y 8/4); breast pale yellow (2.5Y 7/4) with discrete and indistinct spots grayish brown (2.5Y 5/2); belly pale yellow (2.5Y 7/4). The first basic plumage of the isolated population in Llanos de Moxos is similar to that of southern specimens (Río de la Plata and Southern +Brazil +), but with a somewhat yellower cast in the underparts. + + + + +FIGURE 3. +Color variation in the Long-tailed Reed Finch + +Donacospiza albifrons + +due to age and feather abrasion. From left to right: AMNH 321449 (new definitive basic plumage); AMNH 322059 (slightly abraded definitive basic plumage); AMNH 388281 (very abraded definitive basic plumage); AMNH 519693 (new first basic plumage); and AMNH 388282 (abraded juvenal plumage, molting to the first basic plumage). All specimens were collected in the southern range of the species. + + + + +Definitive basic plumage: +Feathers of the crown and nape olive brown (2.5Y 4/3) with the central shafts dark gray (2.5Y 3/1), resulting in a streaked appearance; interscapulars olive brown (2.5Y 4/4) with the central shafts black (2.5Y 2.5/1); rump olive brown (2.5Y 4/3); upper tail coverts olive brown (2.5Y 4/3) with the central shafts black (2.5Y 2.5/1); chin and throat yellow (10YR 8/6); breast and belly yellow (10YR 7/8), sides brownish yellow (10YR 6/6); crissum brownish yellow (10YR 6/6), supercilium and lores pale yellow (2.5Y 8/3); auriculars dark grayish brown (2.5Y 4/2); primaries and secondaries very dark brown (10YR 2/2) edged pale brown (2.5Y 6/4) in the outer vanes; greater wing coverts and tertials very dark brown (10YR 2/2) edged yellowish brown (10YR 5/8) in the outer vanes; marginal wing coverts gray (5Y 5/1); rectrices very dark brown (10YR 2/2) edged light yellowish brown (2.5Y 6/4) in the outer vanes; under wing coverts whitish. +Individual variation: +marked, especially on the intensity of pigmentation. Some specimens from the extreme southern range are comparatively paler than usual for Río de la Plata, as illustrated by an extreme example from +Uruguay +( +USNM +630463), which is as pale as some specimens from the extreme northern range (Southeastern +Brazil +Highlands). +Wear variation: +the overall appearance of the specimen varies considerably with plumage condition, because worn plumage is paler than new plumage. This is due to both plumage fading, which changes the hue of feathers, and abrasion, which progressively shortens the more richly colored distal portion of the feathers’ barbs. Therefore, specimens with very worn plumage become paler throughout, with their underparts becoming light buff, because ventral feathers have a whitish band proximal in relation to the buff tips. The upperparts become progressively less streaked, which is due to the reduction in contrast between the dark central shaft and the paler borders of the dorsal feathers. As a consequence, specimens with worn plumage from Río de la Plata and Southern +Brazil +look like freshly plumaged specimens from Southeastern +Brazil +Uplands. Specimens with worn plumage from Southeastern +Brazil +Highlands show pale yellow (2.5Y 8/2), almost whitish, underparts. +Geographic variation: +the large geographic variation in color observed in this species has a strong clinal component ( +Figure 4 +), but with a remarkable exception for birds from Llanos de Moxos (see below). Generally, birds from the southern portion of the range (Río de la Plata and Southern +Brazil +) are more richly colored, as described above, and birds from the higher areas in the northern portion of the range (Southeastern +Brazil +Highlands) are grayer and paler throughout and less streaked on the upperparts (main differences: birds from Southeastern +Brazil +Highlands show crown and nape dark gray (10YR 4/ 1) and unstreaked; interscapulars dark gray (10YR 4/1), with the central shafts black (2.5Y 2.5/1); chin white (2.5Y 8/1); throat yellow (2.5Y 8/8); breast pale yellow (2.5Y 7/4); belly pale yellow (2.5Y 7/3); sides light olive brown (2.5Y 5/3); primaries and secondaries black (10YR 2/1) edged dark gray (10YR 4/1). Birds from the Southeastern +Brazil +Uplands generally show intermediate coloration (main differences: feathers of the underparts light gray 2.5Y 7/2 or pale yellow 2.5Y 7/3; feathers of upperparts edged olive gray 5Y 4/2 or dark grayish brown 2.5Y 4/2). Birds from Llanos de Moxos are similar to birds from the Southeastern +Brazil +Uplands, only slightly more richly colored, especially in the underparts, but with extremes of variation (e.g. +LSUMZ +124923) much like specimens from Río de la Plata and Southern +Brazil +( +Figure 5 +). + + + + +Body size. +Males and females of the Río de la Plata present similar body measurements ( +Table 1 +) for culmen, tarsus, and tail length, but wing length is significantly longer in males than in females (P <0.001). Mean wing length of males also seems to be longer than those of females for all other groups ( +Figure 6 +), but, given the small sample size, no statistical test was performed. Despite some differences in mean body size between the groups investigated here, considerable overlap in measurements exist between them ( +Table 1 +, +Figure 6 +) and no morphometric characters are diagnostic at a 95% level using the method of +Patten & Unitt (2002) +. + + +The PCA ( +Figure 7 +) demonstrated no clear-cut separation between the populations defined here. The contribution ratios of the first principal component (PC1, with an eigenvalue of 1.99 for males and 2.46 for females) were 49.78% for males and 61.60% for females. The second principal component (PC2, with an eigenvalue of 1.15 for males and 0.91 for females) contributed with 28.80% and 22.80%, respectively. PC1 represents a relationship between culmen and tarsus length, and PC2 represents a relationship between tail and, to a lesser extent, wing length. + + + +FIGURE 4. +Geographic variation in coloration of definitive basic plumaged specimens of the Long-tailed Reed Finch + +Donacospiza albifrons + +. All specimens, from left to right, were collected in the following Brazilian states: DZUFMG 6286— Minas Gerais; MZUSP 78041—São Paulo; MZUSP 28940—São Paulo; MZUSP 2640—São Paulo; MZUSP 19941—São Paulo; MZUSP 2625—São Paulo; MZUP 6915—Paraná; and MZUSP 38792—Rio Grande do Sul. Note the clinal variation in plumage coloration, with northern birds paler and almost unstreaked on the upperparts (left), and with southern birds markedly buff and streaked on the upperparts (right). + + + +The Spearman's correlation coefficient revealed no correlation between body size and mean annual temperature for either males (R = -0.098, P = 0.49) or females (R = -0.041, P = 0.82) ( +Figure 8 +). Birds from Southeastern +Brazil +Highlands averaged larger than birds from the other groups (some overlap in body size does exist), but a linear north-south cline does not describe the variation in body size observed in the species. + + + + + +FIGURE 5. +Color variation in the definitive basic plumage of the Long-tailed Reed Finch + +Donacospiza albifrons + +. From left to right: LSUMZ 60674—Buenos Aires, Argentina (new plumage); LSUMZ 124923—El Beni, Bolivia (new plumage); LSUMZ 124921—El Beni, Bolivia (abraded plumage); and LSUMZ 63122—São Paulo, Brazil (abraded plumage). + + + + +FIGURE 6. +Box plot comparisons between measurements of the five groups of the Long-tailed Reed Finch + +Donacopspiza albifrons + +delimited here (see text). Boxes show the median line and the 25th and 75th percentiles; bars show the non-outlier range of variation. Sample sizes are: RP—Río de la Plata (25♂, 18♀); SB—Southern Brazil (9♂, 8♀); SU—Southeastern Brazil Uplands (8♂, 4♀); SH—Southeastern Brazil Highlands (10♂, 8♀); and LM—Llanos de Moxos (3♂, 1♀). + + + + +FIGURE 7. +Scatterplots of the first versus the second principal component scores of a Principal Component Analysis of the morphometric variables measured from specimens of the Long-tailed Reed Finch + +Donacospiza albifrons + +. Distinct symbols indicate distinct population groups as delimited in the main text. Component loadings are indicated between parentheses along the axis. + + + + +FIGURE 8. +Correlation between body size (measured as the first Principal Component scores) and average mean annual temperature of the collection site of specimens of the Long-tailed Reed Finch + +Donacospiza albifrons + +examined in this study. Component loadings for males are as follow: wing -0.826, tail -0.36, culmen -0.764, and tarsus -0.771, with a contribution ratio of 49.8%. Component loadings for females are as follow: wing -0.865, tail -0.667, culmen -0.804, and tarsus -0.791, with a contribution ratio of 61.6%. + + + + + + +Discussion + + + +Habitat. +The mountainous and comparatively dry habitat where I recorded the Long-tailed Reed Finch in the Southeastern +Brazil +Highlands strongly contrasts with that previously reported for the species, which is said to inhabit low elevation seasonally wet grasslands, southern temperate grasslands, and freshwater marshes ( + +Parker +et al. +1996 + +). The species seems to use distinct habitat +types +in different parts of its range, with southern populations associated with wetter habitats ( +Wetmore 1926 +; +Belton 1994 +; +Narosky & Yzurieta 2003 +), and northern populations associated with drier, mountainous habitats. An exception to this rule is the disjunct population from Llanos de Moxos, which is also associated with lowland seasonally wet grasslands ( + +Maillard +et al. +2008 + +; +Lane 2014 +). I stress that members of all genera closely related to + +Donacospiza + +, such as + +Cypsnagra + +, + +Poospizopsis + +, + +Urothraupis +Taczanowski & von Berlepsch + +, and + +Microspingus + +, are, with few exceptions, associated with open or semiopen habitats far from water, such as open savannas, shrublands, low woodlands, and forest borders, frequently in mountainous areas ( +Fjeldså & Krabbe 1990 +; +Ridgely & Tudor 2009 +). + + + + +TABLE 1. +Morphometric analysis of body measurements of the Long-tailed Reed Finch + +Donacospiza albifrons + +. All measurements are given in mm, except body mass, which is given in g. Given the small sample size for several populations, no statistical comparison between them was performed. + + + + +Variable Sex Llanos de Moxos (LM) Río de la Plata (RP) Southern +Brazil +(SB) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Wing♂ ♀Mean 62.2 60.0SD 0.87 -Min–Max 61.2–62.9 -n 3 1Mean 62.3 58.7SD 1.83 2.92Min–Max 59.2–66.4 53.2–65.7N 25 18Mean 61.6 58.4SD 1.96 1.70Min–Max 58.9–65.5 56.3–61.2n 9 8
Tail Tarsus♂ ♀ ♂66.2 62.3 20.32.90 - 0.3164.1–68.2 62.3 20.0–20.63 1 372.6 70.5 19.94.06 4.39 0.8067.3–82.9 61.0–76.5 18.5–21.324 16 2570.3 66.6 19.92.48 3.62 0.7467.1–76.0 63.3–74.5 18.8–21.19 8 9
Culmen♀ ♂ ♀20.6 14.8 14.4- 0.23 -20.6 14.5–14.9 -1 3 119.8 13.1 13.10.92 0.50 0.9218.5–21.6 12.2–14.2 18.5–21.617 24 1819.1 13.5 13.50.62 0.43 0.2118.2–19.8 13.0–14.3 13.2–13.88 9 7
Body mass18.90.7618.1–19.6314.71.4813.7–16.43----
+ +16.1--114.20.2414.0–14.5415.0--1
+
+ +continued. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
VariableSexSoutheasternBrazilianUplands (SU)SoutheasternBrazilianHighlands (SH)
MeanSDMin–MaxnMeanSDMin–Maxn
Wing + +62.70.8461.7–64.3865.42.5862.3–69.4 +10 +
+ +60.40.6159.6–61.0461.41.2959.9–63.98
Tail + +72.52.9568.1–76.2874.22.7669.6–79.0 +10 +
+ +72.22.7668.3–74.3471.04.2163.7–74.77
Tarsus + +20.70.8319.2–21.4821.40.8019.7–22.8 +8 +
+ +20.30.5819.7–20.8420.71.1819.6–22.78
Culmen + +14.10.5913.2–14.9814.60.4313.9–15.3 +10 +
+ +13.90.1713.7–14.1414.60.5913.9–15.78
Body mass + +15.5-15.5118.81.4417.5–21.0 +6 +
+ +----17.80.5017.2–18.55
+
+ + +Breeding season. +Comprehensive data on the breeding biology of the species is lacking, but the incubation period is 13 days and the nestling period is 12 days ( +Di Giacomo 2005 +). The breeding season estimated from gonadal data on the labels of museum specimens (Sep–Jan) agrees with the scattered information available in the literature. Data from the southern range of the Long-tailed Reed Finch suggest nesting from Sep–Mar, with birds in breeding condition collected from Sep–Jan ( +Gibson 1885 +; +Hartert & Venturi 1909 +; +Wetmore 1926 +; +Pereyra 1938 +; + +Darrieu +et al. +1988 + +; +Belton 1994 +; +Darrieu & Camperi 1996 +; +Di Giacomo 2005 +; de la +Peña 2013 +; + +Pretelli +et al. +2013 + +; data presented here). An adult was observed feeding a juvenile + +Molothrus bonariensis + +on +2 Feb 1986 +( +Di Giacomo & Aguilar 1987 +). Therefore, breeding of the southern populations extends from Sep–Mar, and even later in +Argentina +, as indicated by specimens with enlarged testes from +5 Jun +( +Darrieu & Camperi 1996 +) and a juvenile (NHMUK 1897.11.14.35) collected on +29 Jun. +The scarce breeding data from the isolated population in Llanos de Moxos suggests a similar breeding season, with two family groups feeding fledglings on +7 Sep 2013 +( +Lane 2014 +) and males with enlarged testes in Oct ( +Schimitt & Schimitt 1987 +). A “juvenil” bird was observed in +Bolivia +in Jul ( + +Maillard +et al. +2008 + +). + + + + +Plumage sequence and molts. +Retention of the juvenal plumage for about 1–2 months after leaving the nest is a common pattern in temperate +Thraupidae +and, even though molt is poorly known in Neotropical passerines ( +Ryder & Durães 2005 +), this same pattern seems to apply to the Long-tailed Reed Finch. +Ryder & Durães (2005) +emphasized that a very distinct juvenal plumage, like that reported here, has been described for a few genera of tanagers, but this conclusion applies only to the traditional systematic arrangement of the family. With the recent and widespread use of molecular data, the systematic arrangement of +Thraupidae +has changed dramatically, with the inclusion in the family of many genera traditionally considered finch-billed New World sparrows ( + +Barker +et al. +2013b + +; + +Burns +et al. +2014 + +, +2016 +). This systematic rearrangement revealed that many genera of the currently recognized +Thraupidae +have a very distinct juvenal plumage, as demonstrated by members of several genera of Poospizini ( +Fjeldså & Krabbe 1990 +; +Rising 2011 +). + + + + +Morphological variation. +Data summarized here demonstrate that the alleged sexual dichromatism previously reported in the species is a misinterpretation of morphological variation due to age, plumage condition, and geography. Geographic variation in the species is somewhat clinal, with smaller, more richly colored birds found in wet lowlands at southern localities and larger, paler birds found in dry highlands at northern localities. Nevertheless, there are several exceptions to this rule, best exemplified by the northernmost population isolated in the seasonally wet grasslands of Llanos de Moxos, which is more richly colored than expected by range. This pattern is also complicated by a large amount of individual variation, best exemplified by the abnormally pale specimens from +Uruguay +discussed above. Gloger’s rule, the tendency for populations in wetter areas to be more heavily pigmented than populations in drier areas ( +Gloger 1833 +; +Zink & Remsen 1986 +), might be a possible explanation for the geographical pattern of color variation in the species, with darker and more richly colored populations found in wet areas, and lighter and paler populations found in drier areas. Even though this ecogeographical rule has been reported for other Neotropical bird species ( +Hayes 2001 +; +Bolívar-Leguizamón & Silveira 2015 +), this hypothesis requires further investigation. + + +Conclusion. +I conclude that, with no solid basis for splitting the species into two or more taxa, the Long-tailed Reed Finch should be considered a single, highly polymorphic species, widely distributed across an extensive area in south-central South America, where it inhabits a wide range of habitat +types +. The marked geographic variation of the Long-tailed Reed Finch remained overlooked until now, apparently due to: 1) the small number of specimens available in museums; 2) the narrow geographic coverage of specimens in all major ornithological collections; and 3) the lack of modern revisions of the taxonomy and morphology of the species, although the nature of morphological variation in the Long-tailed Reed Finch was disputed for decades. This study is another example of how poorly understood the alpha taxonomy and the morphological and geographic variation of Neotropical birds remains (e.g. +Lopes & Gonzaga 2014 +, +2016a +, +b +; +Lopes 2017 +). This poor level of knowledge represents a key impediment to a thorough accounting of Neotropical bird diversity. + + +
+
+
\ No newline at end of file diff --git a/data/38/67/4C/38674CEDB56E4D9BE6A0FBCA0AF0B211.xml b/data/38/67/4C/38674CEDB56E4D9BE6A0FBCA0AF0B211.xml new file mode 100644 index 00000000000..fcb26125e32 --- /dev/null +++ b/data/38/67/4C/38674CEDB56E4D9BE6A0FBCA0AF0B211.xml @@ -0,0 +1,233 @@ + + + +Arthropoden aus südostalpinen Höhlen + + + +Author + +Karl W. Verhoeff + +text + + +1933 +W. JUNK + +Berlin W. 15 + + + +MITTEILUNGEN über Höhlen- und Karstforschung Zeitschrift des Hauptverbandes Deutscher Höhlenfqrscher Jahrgang 1933 + + + +1 +21 + + + + +http://un.availab.le + +book chapter +Verhoeff-1933-full-article + + + + + +Troglarmadillidium (Illyricosphaera +n. subg. +) subterraneum + +n. sp. + + + + +♂ +2 2/3-2 3/4 mm +. ♀ fast +4 mm +lang. +Koerper +pigmentlos, weiss, aber durch anhaftende +Fremdkoerper +stellenweise +braeunlich +erscheinend. Ocellen fehlen ganz. Kopf und auch die einfach beborsteten Antennen mit dichter, wabiger +Waerzchenstruktur +. 2. Geisselglied dreimal +laenger +als das 1. + + + + +Die Mundwerkzeuge sind denen der Gattungsgenossen sehr +aehnlich +, die Mandibeln entsprechen fast +vollstaendig +der Abb. 257 und 258 in + +RACOVITZA's Isopodes terrestres, +I. ser +. +1907 +, + +Archives Zool +exper +. et +gener +. + + +, doch besteht der Hauptzahn der linken Mandibel aus zwei +staerkeren +und zwei +schwaecheren +Vorspruengen +, der glasige Vorzahn der rechten Mandibel springt dreieckig nach innen vor. + + + + +1. Trunkus-Epimeren am Seitenrande vor der Hinterecke gerade, der Hinterrand des 1. Tergit (Abb. 2 und 4) jederseits leicht eingebuchtet. Borsten der Tergite vorwiegend ziemlich lang und gebogen, an den +Seitenraendern +kuerzer +, +ueber +die ganze +Flaeche +am ganzen +Ruecken +dicht verstreut. Rundliche bis ovale +Gruebchen +(Abb. 3) zwischen den Borsten sind teils +vollstaendig +, teils +unvollstaendig +fein gerandet und +ueber +den +groessten +Teil der Tergite verstreut. +Waerzchen +dagegen finden sich nur vorn im mittleren Gebiet. Die +Laeppchen +(lo Abb. 4) unten an den 1. Epimeren sind vom Vorderrand doppelt so weit wie vom Hinterrand entfernt, die anschliessende Leiste +laeuft +vollstaendig +durch bis zum +gegenueberliegenden +Laeppchen +. Oben +verlaeuft +innen am Seitenrande der 1. Epimeren in der ganzen +Laenge +eine gebogene Furche. Von +Epimerendruesen +habe ich nichts bemerkt. + + +2. Epimeren aussen abgerundet, ihr +Laeppchen +vom Vorderrand 1 1/2 mal weiter als vom Hinterrand entfernt und die anschliessende Leiste (k Abb. 5) +laeuft +auch hier +ueber +die Mitte +vollstaendig +durch. + + +7. Tergit mit abgerundet-rechtwinkeligen Hinterecken, mit vielen +Gruebchen +, aber ohne +Waerzchen +. + + +1. Beinpaar am Karpopodit innen mit dichter Grannenmasse (Putzapparat), unten mit zahlreichen Stachelborsten, von welchen die 2 obersten, dem Endrand +genaeherten +, in 4-5 Spitzen zerteilt sind. Propodit unten mit 4 Stachelborsten, aber ohne +Putzkaemmchen +. 7. Beinpaar des + +ohne Auszeichnung, Stachelborsten unten am Karpo- und Propodit einfach. + + +Telson hinten breit abgerundet (Abb. 6), die Seiten leicht bogig. Uropodenpropodite (Abb. 7) aussen und innen +kraeftig +eingebuchtet, unten warzig, die Endopodite +ueberragen +etwas die Exopodite, welche etwa 1 3/5 mal breiter als lang hinten innen und aussen +gleichmaessig +zugerundet sind. + + +Die 1. Pleopoden des ♂ (Abb. 8) sind von recht einfacher Beschaffenheit, indem die kleinen, etwas +schraeg +gestellten, quer-ovalen Exopodite +ueberhaupt +gar nicht nach hinten ausgezogen sind. Die Endopodite +verschmaelern +sich schnell nach hinten und laufen in einen schmalen, aber stumpfen Endzipfel aus. + + +Im +groessten +Gegensatz zu den 1. sind die Exopodite der 2. Pleopoden nach hinten in lange, dreieckige Zipfel ausgezogen, aussen hinten weit eingebuchtet, davor noch mit einer kleineren Trachealfeld-Einbuchtung. Die 2. Endopodite sind in lange, +duenne +, am Ende spitze Spiesse ausgezogen, welche die Exopodite sehr weit +ueberragen +. + + +Hinsichtlich der Gestalt des Kopfes (Abb. 1) sei noch Folgendes +erwaehnt +: + + +Statt vorragender Antennenlappen finden sich einfache +Schraegleisten +. Ein eigentliches Stirndreieck ist nicht ausgebildet, aber ein +Y-foermiger +Wulst, d. h. der Absturz mit medianem Wulst gegen den Clypeus ist vorhanden und an ihn schliessen sich nach oben Abdachungen an, die unter fast rechtem Winkel unten zusammenstossen und in den medianen Wulst +uebergehen +. Zwei gebogene Stirn-Seitenleisten jederseits sind besonders dadurch kenntlich, dass sich an ihnen das Gerinnsel auf dem Kopfe festsetzt. + + + + + +Vorkommen: Am + +26. IV. 33 + +sammelte mein +Freund K. SRASSER +( +Triest +), dem ich bereits zahlreiche wertvolle Funde zu verdanken habe, bei +Madonna del Carso in Westistrien +2♂ +, +1♀ +unter grossen, auf Roterde liegenden Kalkplatten, am Fusse von Mauern, neben Stoppelfeld mit Oliven bei Regen in + +80 m + +Hoehe +. - Es ist nicht unwahrscheinlich, dass diese Form auch noch in +Hoehlen +gefunden wird + +. + + + + \ No newline at end of file diff --git a/data/38/67/A9/3867A96A6527D6E46B17513C73A69F64.xml b/data/38/67/A9/3867A96A6527D6E46B17513C73A69F64.xml new file mode 100644 index 00000000000..24bf346131d --- /dev/null +++ b/data/38/67/A9/3867A96A6527D6E46B17513C73A69F64.xml @@ -0,0 +1,411 @@ + + + +Info Flora Schweiz - Fabaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/fabaceae.html + +url + + + + + +Medicago arabica +(L.) Huds. + + + + + +Arabischer Schneckenklee + + + + +Art ISFS: 254900 Checklist: 1028490 +Fabaceae +Medicago +Medicago arabica (L.) Huds. + + + +Bestimmungsschluessel + + + +Zusammenfassung + + + + +Artbeschreibung + +(nach +Lauber & al. 2018 +) + +: +Staengel +15-60 cm +, niederliegend, aufsteigend oder aufrecht, abstehend behaart. +Teilblaetter +breit +verkehrt-herzfoermig +, ca. +15 mm +lang und +12 mm +breit, in der Mitte +mit einem braunen Fleck +(nur bei dieser +M.- +Art). +Nebenblaetter +grob +gezaehnt +. + +Blueten +gelb, +Bluetenstand +nur 1-5 +bluetig + +. Frucht +/- kugelig, mit 3-6 Schraubenwindungen und bis +4 mm +langen, oft +gekruemmten +Stacheln, Durchmesser +4-7 mm +. + + + + +Bluetezeit + +(nach +Lauber & al. 2018 +) + +: 4-5 + + +Standort und Verbreitung in der Schweiz + +(nach +Lauber & al. 2018 +) + +: +Aecker +, +Schuttplaetze +/ kollin / Sehr zerstreut in J, M, A + + + + +Verbreitung global + +(nach +Lauber & al. 2018 +) + +: Mediterran + + + + +Oekologische +Zeigerwerte + +(nach +Landolt & al. 2010 +) + +234+452.k-t.2n=16 + + + + + +Oekologie + + +Lebensform Monokarper Hemikryptophyt, Therophyt + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + + + + + +
KEINE ANGABE
+
+
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +maessig +trocken +Lichtzahl LhellSalzzeichen1
Reaktionszahl Rschwach sauer bis neutral (pH 4.5-7.5)Temperaturzahl T +sehr warm-kollin (nur an +waermsten +Stellen, Hauptverbreitung in +Suedeuropa +) +
+Naehrstoffzahl +N + +naehrstoffreich + +Kontinentalitaetszahl +K +subozeanisch (hohe Luftfeuchtigkeit, geringe Temperaturschwankungen, eher milde Winter)
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Medicago arabica +(L.) Huds. + + + + + + +Volksname Deutscher Name: +Arabischer Schneckenklee +Nom +francais +: +Luzerne d'Arabie +Nome italiano: +Erba medica araba + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Medicago arabica (L.) Huds. + + +Checklist 2017 + +254900
= +Medicago arabica (L.) Huds. + + +Flora Helvetica 2001 + +1112
= +Medicago arabica (L.) Huds. + + +Flora Helvetica 2012 + +620
= +Medicago arabica (L.) Huds. + + +Flora Helvetica 2018 + +620
= +Medicago arabica (L.) Huds. + + +Index synonymique 1996 + +254900
= +Medicago arabica (L.) Huds. + + +Landolt 1977 + +1751
= +Medicago arabica (L.) Huds. + + +SISF/ISFS 2 + +254900
= +Medicago arabica (L.) Huds. + + +Welten & Sutter 1982 + +874
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Status Indigenat +: Neophyt: nach der Entdeckung von Amerika in der Region aufgetreten (nach 1500) + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein + + +
+
\ No newline at end of file diff --git a/data/38/67/E0/3867E07487B8F9E1B17B6F5C0BE599F4.xml b/data/38/67/E0/3867E07487B8F9E1B17B6F5C0BE599F4.xml new file mode 100644 index 00000000000..fffc982f1e5 --- /dev/null +++ b/data/38/67/E0/3867E07487B8F9E1B17B6F5C0BE599F4.xml @@ -0,0 +1,82 @@ + + + +New ants from southeastern and central Brazil (Hymenoptera, Formicidae). + + + +Author + +Kempf, W. W. + +text + + +Studia Entomologica (N. S.) + + +1967 + +9 + + +121 +128 + + + + +http://antbase.org/ants/publications/4581/4581.pdf + +journal article +4581 + + + + +Trachymyrmex dichrous +n. sp. + + + +(Figs. 7-9) +Worker (holotype). - Total length 5.0 (4.5-5.1) mm; head length 1.04 (0.99-1.07) mm; head width 0.99 (0.88-1.01) mm; maximum diameter of eyes 0.21 (0.17-0.22) mm; scape length 1.04 (0.93-1.07) mm; thorax length 1.65 (1.51-1.70) mm; petiole length 0.40 (0.35-0.40) mm; petiole width 0.24 mm; postpetiole length 0.38 (0.29-0.38) mm; postpetiole width 0.43 (0.40-0.43) mm; hind femur length 1.65 (1.49-1.70) mm. Head capsule black, rest of body medium brown, scapes and gaster with reddish hues. Long, yellowish brown, silky hairs abundant on head, thorax and pedicel, where they are recurved; same hairs, less recurved and more bristle-like on gaster, strictly oblique on scapes and legs. Dense pubescence of lighter color inclined or appressed on head, pedicel, gaster and appendages, erect or suberect on thorax, but never masking the integument. +Head as shown in Fig. 7. Mandibles smooth and shining except laterally on. base where they are finely striate; chewing border with approximately 9 teeth. Head capsule very finely granulate, opaque. Clypeus antero-mesially notched. Frontal lobes triangular, frontal carinae diverging caudad, fading out at posterior third of head. Front and vertex inconspicuously tuberculate, integument rough. Preocular carinae not curving mesad above eyes, but fading out somewhat behind eyes. Posterior half of antennal scrobe indistinct. Supraocular tumulus more or less vestigial; occipital corners likewise not prominent but rounded and edentate. Occiput in full-face view distinctly notched in the middle. No carinae on vertex. Inferior occipital corner indistinctly marginate and rounded. Inferior border of cheeks practically immarginate. Eyes moderately convex, more than 15 facets across greatest diameter. Scapes of antennae as long as head capsule, greatly surpassing occipital corner. All funicular segments decidedly longer than broad. +Thorax as shown in Fig. 8. Integument subopaque but sculpture indistinct. Hairs not arising from prominent tubercles. Pronotum with indistinct humeral angle, antero-inferior corner rounded, lateral teeth low, mesial teeth absent. Mesonotum with rather prominent anterior conical spines, facing obliquely laterad, followed by two pairs of small denticles, the posterior pair almost indistinct. Thorax constricted dorso-laterally at mesoepinotal junction, lacking a suture. Basal face of epinotum narrow, laterally indistinctly marginate; anteriorly indistinctly, posteriorly distinctly dentate; the latter representing the extremely short and inconspicuous epinotal spines. Epinotal stigma prominent. Femora thin, cylindrical, hind femora about as long as thorax. +Petiole and postpetiole as shown in Figs. 8 and 9. Piligerous tubercles prominent. Petiole pedunculate, node proper twice as broad as peduncle. Postpetiole flattened above, with a deep postero-median excision. Gaster opaque, with minute piligerous tubercles rather evenly distributed. Tergite I antero-laterally vestigially marginate. +Female and male unknown. + + +Specimens examined: 22 workers, as follows: Brasil, Goias State, Anapolis, January 7, 1966, W. W. Kempf leg. 16 workers (holotype and paratypes, WWK n. 4230); same locality but different nest, January 4, 1966, W. W. Kempf leg. 4 workers (paratypes, WWK n. 4199); Sao Paulo State, Agudos, December 13, 1955, W. W. Kempf leg. 1 worker (paratype, WWK n. 1493); Mato Grosso State: Chapada, May 1959, C. Amann leg. 1 worker (WWK, paratype). + + + +Discussion. - Although highly distinctive, +dichrous +belongs to the species-group which is characterized by smooth mandibles, by a more or less defined antennal scrobe, by rather straight preocular carinae that do not curve mesad above eyes, by the lack of a basal lobe on antennae. This group comprises by far the greatest number of species in the genus. + + +Within this group, +dichrous +may at once be recognized by the ensemble of the following characters: triangular frontal lobes, lack of paired carinae on vertex, lack of an inferior occipital spine or tooth, lack of midpronotal teeth, lack of conspicuous tubercles on thorax, postero-dorsal border of postpetiole deeply excised. In addition, +dichrous +has the antero-inferior angle of pronotum rounded, a character which is only found in +isthmicus +and another still undescribed but otherwise completely different species. +T. isthmicus +differs from +dichrous +in the shape of the frontal lobes, the completely margined antennal scrobe, the presence of midpronotal teeth, the quadricarinate tergum I of the gaster. The same characters, plus the dentate antero-inferior pronotal corner, separate +oetkeri +and +urichi +, the closest sympatric species, from +dichrous +. + + + +The present species, which was found in Anapolis near km 46 of the Goiania highway, in a scrub-covered xerophilus woodland ("cerrado") by the gravel road leading to Leopoldo Bulhoes, at an altitude over 1000 m. The single nest entrance was surrounded by a sizeable crater of loosely heaped up earth crumbs. The lone stray worker from Agudos was taken from the ground in open and rather dry parkland. Hence it is probable that this species is a typical denizen of the vast "campos", that characterize the vegetation of central Brazil. + + + \ No newline at end of file diff --git a/data/38/68/0A/38680AAE1C6036B642269C7DEFEF6447.xml b/data/38/68/0A/38680AAE1C6036B642269C7DEFEF6447.xml new file mode 100644 index 00000000000..9544f293b55 --- /dev/null +++ b/data/38/68/0A/38680AAE1C6036B642269C7DEFEF6447.xml @@ -0,0 +1,131 @@ + + + +A new genus of Coelotinae (Araneae, Agelenidae) from southern China + + + +Author + +Chen, Lu + + + +Author + +Li, Shuqiang + + + +Author + +Zhao, Zhe + +text + + +ZooKeys + + +2015 + +541 + + +41 +56 + + + + +http://dx.doi.org/10.3897/zookeys.541.6678 + +journal article +http://dx.doi.org/10.3897/zookeys.541.6678 +1313-2970-541-41 +29AD6025C7F04E998DAE6DF09827545B +29AD6025C7F04E998DAE6DF09827545B + + + +Taxon classification Animalia Araneae Agelenidae + + + +Genus +Flexicoelotes +gen. n. + + + +Type species. + +Flexicoelotes jiaohanyanensis +sp. n. + + + +Etymology. + +The generic name is derived from the +species' +similarity to +Coelotes +and the Latin adjective +"flexus" +, meaning "bent, curved", referring to the shape of the conductor. The gender is masculine. + + + +Diagnosis. + +Males can be easily distinguished from other coelotines, except +Tonsilla +Wang & Yin, 1992 and +Lineacoelotes +Xu, Li & Wang, 2008, by the broad conductor, the spoon-like median apophysis, and the elongate cymbial furrow. They can be distinguished from +Tonsilla +by the bent conductor apex, rather than a lobed conductor, the presence of an anterior apophysis, and the broad cymbial furrow (Fig. 2 +A-C +; +Wang and Yin 1992 +: figs 3-5). They can be distinguished from +Lineacoelotes +by the broad, bent and less modified conductor, the presence of an anterior apophysis, and the thin, simple patellar apophysis (Fig. 2 +A-C +; +Xu et al. 2008 +: figs 13-15). Females can be easily distinguished from other coelotines, except +Tonsilla +and +Lineacoelotes +, by the long epigynal teeth and the absence of epigynal hoods. They can be distinguished from +Tonsilla +by the large and simple atrium, rather than a posteriorly extended anterior atrial margin, an atrium with the anterior part wider than the posterior part, epigynal teeth that are separated rather than near one another, the short and posteriorly located +spermathecae +, and the broad, long copulatory ducts (Fig. 3 +A-B +; +Wang and Yin 1992 +: figs 8-10). They can be distinguished from +Lineacoelotes +by the large atrium, the short, simple spermathecae, and the absence of a long, coiled spermathecal head (Fig. 3 +A-B +; +Xu et al. 2008 +: figs 11-12). + + + +Description. + +Flexicoelotes +are small to medium-sized, with a total length of 4-9 mm; chelicerae with three promarginal and two retromarginal teeth; male palp with one patellar apophysis; RTA with pointed tip, extending beyond the distal margin of the tibia; LTA short; conductor broad and wider than tibia; median apophysis spoon-like; anterior apophysis present; epigynal teeth very long; atrium large; spermathecae simple, located posteriorly; copulatory ducts broad, located dorsal to the spermathecae. + + + +Distribution. +China (Yunnan, Guangxi) (Fig. 9). + + + \ No newline at end of file diff --git a/data/38/68/95/3868956607C859A4BCD1884912FBF000.xml b/data/38/68/95/3868956607C859A4BCD1884912FBF000.xml new file mode 100644 index 00000000000..70b12b96137 --- /dev/null +++ b/data/38/68/95/3868956607C859A4BCD1884912FBF000.xml @@ -0,0 +1,465 @@ + + + +Revision of the Exechia parva group (Diptera: Mycetophilidae) + + + +Author + +Lindemann, Jon Peder +https://orcid.org/0000-0001-6001-7910 +UiT - The Arctic University of Norway, Tromso, Norway +jon.p.lindemann@uit.no + + + +Author + +Soli, Geir +https://orcid.org/0000-0001-5301-6995 +Natural History Museum, Oslo, Norway +geir.soli@nhm.uio.no + + + +Author + +Kjaerandsen, Jostein +https://orcid.org/0000-0002-3104-073X +UiT - The Arctic University of Norway, Tromso, Norway +jostein.kjarandsen@uit.no + +text + + +Biodiversity Data Journal + + +2021 + +2021-09-24 + + +9 + + +67134 +67134 + + + + +http://dx.doi.org/10.3897/BDJ.9.e67134 + +journal article +http://dx.doi.org/10.3897/BDJ.9.e67134 +1314-2828-9-e67134 +A1151C0727B74F31BC4B6809DA6F87CD +54EEB1B3D94E5239B847CC1AD9587A36 + + + + +Exechia longilobata Lindemann +sp. n. + + + +Materials + + +Type status: + +Holotype +. + +Occurrence +: + +catalogNumber: +TSZD-JKJ-102235 +; recordedBy: + +Bo W. Svensson +et al. + +; individualCount: +1 +; sex: +male +; lifeStage: +adult +; preparations: +Pinned +, with genitalia in glycerine in separate microvial; + +Location +: + +country: +Sweden +; county: + +Skane + +; municipality: + +Malmoe + +; locality: + +Limhamns +kalkbrott + +; verbatimElevation: + +- + +40 m + + +; decimalLatitude: +55.5681 +; decimalLongitude: +12.9241 +; + +Event +: + +samplingProtocol: +Malaise Trap +; eventDate: +2011-11-15 +; habitat: Limestone quarry; +Record Level: +institutionCode: TMU + +Type status: + +Paratype +. + +Occurrence +: + +catalogNumber: +TSZD-JKJ-259573 +; recordedBy: + +B. W. Svensson +& +Co. + +; individualCount: +1 +; sex: +male +; lifeStage: +adult +; preparations: +Pinned +, with genitalia in glycerine in separate microvial; + +Location +: + +country: +Sweden +; county: + +Skane + +; municipality: + +Malmoe + +; locality: + +Limhamns +kalkbrott + +; verbatimElevation: + +- + +40 m + + +; locationRemarks: MT 1 - "grafitti"; decimalLatitude: +55.56826 +; decimalLongitude: +12.92408 +; + +Event +: + +samplingProtocol: +Malaise trap +; eventDate: +2011-11-01 +/ +2011-11-30 +; habitat: Limestone quarry; +Record Level: +institutionCode: TMU + +Type status: + +Paratype +. + +Occurrence +: + +catalogNumber: +SPM-054527 +; recordedBy: + +Bo W. Svensson +et al. + +; individualCount: +1 +; sex: +male +; lifeStage: +adult +; preparations: +Pinned +, with genitalia in glycerine in separate microvial; + +Location +: + +country: +Sweden +; county: + +Skane + +; municipality: + +Malmoe + +; locality: + +Limhamns +kalkbrott + +; verbatimElevation: + +- + +40 m + + +; locationRemarks: MT2 - "planen"; decimalLatitude: +55.5681 +; decimalLongitude: +12.9241 +; + +Event +: + +samplingProtocol: +Malaise Trap +; eventDate: +2009-04-23 +/ +2009-05-10 +; habitat: Limestone quarry; +Record Level: +institutionCode: TMU + +Type status: + +Paratype +. + +Occurrence +: + +catalogNumber: +SPM-058935 +; recordedBy: + +Bo W. Svensson +et al. + +; individualCount: +1 +; sex: +male +; lifeStage: +adult +; preparations: +Pinned +, with genitalia in glycerine in separate microvial; + +Location +: + +country: +Sweden +; county: + +Skane + +; municipality: + +Malmoe + +; locality: + +Limhamns +kalkbrott + +; verbatimElevation: + +- + +40 m + + +; decimalLatitude: +55.56826 +; decimalLongitude: +12.92408 +; + +Event +: + +samplingProtocol: +Malaise trap +; eventDate: +2012-02-29 +/ +2012-03-30 +; habitat: Limestone quarry; +Record Level: +institutionCode: TMU + + + + + + + + + + + +Description + +Male (n = 4): Body length 3.0-3.1 mm. Wing length 2.5 mm. +Colouration +(Dry specimen). Head, face and clypeus dark brown; labellum yellow; palpus yellow. Antenna with scape and pedicel yellow; flagellum yellow. Thorax with scutum and lateral sclerites brown; propleura pale brown; halteres whitish-yellow, apically slightly darker. Legs yellow. Abdomen brown with tergite II slightly paler or with pale area covering its ventral half. Terminalia yellow. +Head +. Frons, vertex and clypeus covered with pale setae. Antenna short, 1.53-1.64 times as long as length from vertex to ventral margin of clypeus; flagellomeres quadrate, with sixth flagellomere 0.9-0.95 times as long as wide. +Thorax +. Scutum covered with pale setae. +Legs +. Fore leg with tibia 0.96-1.1 times as long as first tarsomere. Mid-tibia (n = 1) with 19 anterior, 4 posterodorsal, 7 posterior and 2 posteroventral bristles. Hind tibia (n = 1) with 7 anterodorsal and 2 posterodorsal bristles. +Wings +. Vein r-m 2.5-3.1 times longer than stem of M-fork. +Abdomen. +Tergites covered with pale setae. +Terminalia +(Fig. +25 +). Each part of divided tergite IX with about 7-9 setae, most apical seta stout. GL with length 0.4-0.54 of gonocoxite width, apico-internal margin slightly angled exteriorly, basal third covered with setae, apex with 3 setae (Fig. +25 +a +, +b +). Aedaegal guides somewhat elongated, evenly tapered, acute apex (Fig. +25 +a +, +b +). Hypandrium covered with 25-31 setae, with the apical pair reaching about two-thirds of GL (Fig. +25 +a +, +b +). Hypandrial lobe with each branch with apical half distinctly widened with apex somewhat acute (Fig. +25 +a +, +b +). Gonostylus with DB (Fig. +25 +c +) 3.0-3.2 times longer than broad, slightly curved interiorly; apical lobe well defined, elongated, narrow, apex rounded; evenly covered with setae on dorsal side, except on most apical part; medio-external margin forming distinct angle, with row of 4 elongate setae. VB apically rounded with 2 small setae. IB apically with 1 seta close to apex and pair of setae one-third from apex. MB apex acute with 1 seta close to the base. + +Female: Unknown. + + +Diagnosis + +Distinguished from + +E. spatulata + +in having the dorsal gonostylus branch more narrow, not spathulate, only 3-3.2 times longer than broad (Fig. +25 +c +), the hypandrium more setose with 25-31 setae (Fig. +25 +a +), each part of the hypandrial lobe with apical half expanded to a wide disc (Fig. +25 +a +), the aedaegal guides evenly tapered (Fig. +25 +a +) and the gonocoxal lobe length only 0.4-0.52 times the gonocoxite width (Fig. +25 +a +, +b +); from other species in the + +E. parva + +group in having the dorsal gonostylus branch more elongate (Fig. +25 +c +), the hypandrial lobe with apical half of each branch widened (Fig. +25 +a +) and the gonocoxal lobes with apico-internal margin slightly angled exteriorly (Fig. +25 +a +). + + + +Etymology + +From Latin +longus +, long and +lobatus +, with lobes, relating to the long apical part of the dorsal branch of the gonostylus. + + + +Distribution + +West Palaearctic, Sweden (Fig. +15 +) + + + +Biology +Adults collected in limestone quarry. + + + \ No newline at end of file diff --git a/data/38/68/9E/38689E41FB8DD3F796CBADDCC89C3A45.xml b/data/38/68/9E/38689E41FB8DD3F796CBADDCC89C3A45.xml new file mode 100644 index 00000000000..d43328d598b --- /dev/null +++ b/data/38/68/9E/38689E41FB8DD3F796CBADDCC89C3A45.xml @@ -0,0 +1,87 @@ + + + +An annotated checklist of the scale insects of Iran (Hemiptera, Sternorrhyncha, Coccoidea) with new records and distribution data + + + +Author + +Moghaddam, Masumeh + +text + + +ZooKeys + + +2013 + +334 + + +1 +92 + + + + +http://dx.doi.org/10.3897/zookeys.334.5818 + +journal article +http://dx.doi.org/10.3897/zookeys.334.5818 +1313-2970-334-1 + + + + +Diaspidiotus turanicus (Borchsenius) + + + + +Aspidiotus turanicus +Borchsenius, 1935: 131. + + + +Iran localities. +Elborz, Kerman, Khorasan -e Shomali, Lorestan, Tehran, Zanjan. + + +Host plants. + +Salicaceae +: +Populus +sp., +Salix +sp. + + + +References. + +Ben-Dov et al. (2013) +, +Farahbakhsh (1961) +, +Kaussari (1955) +, +Kaussari and Farahbakhsh (1968) +, + +Kozar +et al. (1996) + +, +Moghaddam (2004) +, +Moghaddam and Tavakoli (2010) +and +Seghatoleslami (1977) +. + + + + \ No newline at end of file diff --git a/data/38/68/D4/3868D4232486FE298F2BCC2334E0AA98.xml b/data/38/68/D4/3868D4232486FE298F2BCC2334E0AA98.xml new file mode 100644 index 00000000000..27b26ba14ca --- /dev/null +++ b/data/38/68/D4/3868D4232486FE298F2BCC2334E0AA98.xml @@ -0,0 +1,135 @@ + + + +Inventory of the Heteroptera (Insecta: Hemiptera) in Komaba Campus of the University of Tokyo, a highly urbanized area in Japan + + + +Author + +Ishikawa, Tadashi + + + +Author + +Saito, Masayuki U. + + + +Author + +Kishimoto-Yamada, Keiko + + + +Author + +Kato, Toshihide + + + +Author + +Kurashima, Osamu + + + +Author + +Ito, Motomi + +text + + +Biodiversity Data Journal + + +2015 + +3 + + +4981 +4981 + + + + +http://dx.doi.org/10.3897/BDJ.3.e4981 + +journal article +http://dx.doi.org/10.3897/BDJ.3.e4981 +1314-2828-3-4981 + + + + +Castanopsides hasegawai Yasunaga, 1992 + + + +Materials + + +Type status: +Other material +. Occurrence: recordedBy: +T. Ishikawa +; individualCount: +1 +; sex: +1 female +; lifeStage: +adult +; otherCatalogNumbers: 2014-00559; Taxon: namePublishedIn: 1992; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hemiptera; family: Miridae; genus: Castanopsides; specificEpithet: hasegawai; scientificNameAuthorship: Yasunaga; Location: country: +Japan +; stateProvince: Tokyo; municipality: Meguro-ku; locality: +The University of Tokyo Campus, Komaba. +; minimumElevationInMeters: 31; maximumElevationInMeters: 39; decimalLatitude: +35.66006 +; decimalLongitude: +139.68521 +; geodeticDatum: WGS84; Identification: identifiedBy: T. Ishikawa; dateIdentified: 2013; Event: samplingProtocol: +light trap +; eventDate: +2013-05-10 +; Record Level: institutionCode: +KMUT +; collectionCode: +IC + + + + +Type status: +Other material +. Occurrence: recordedBy: +T. Ishikawa +; individualCount: +2 +; sex: +2 females +; lifeStage: +adult +; otherCatalogNumbers: 2014-00560 | 2014-00561; Taxon: namePublishedIn: 1992; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hemiptera; family: Miridae; genus: Castanopsides; specificEpithet: hasegawai; scientificNameAuthorship: Yasunaga; Location: country: +Japan +; stateProvince: Tokyo; municipality: Meguro-ku; locality: +The University of Tokyo Campus, Komaba. +; minimumElevationInMeters: 31; maximumElevationInMeters: 39; decimalLatitude: +35.66006 +; decimalLongitude: +139.68521 +; geodeticDatum: WGS84; Identification: identifiedBy: T. Ishikawa; dateIdentified: 2013; Event: samplingProtocol: +net sweeping +; eventDate: +2013-05-18 +; Record Level: institutionCode: +KMUT +; collectionCode: +IC + + + + + \ No newline at end of file diff --git a/data/38/68/F0/3868F0593041F2DA290311E682BCC5D1.xml b/data/38/68/F0/3868F0593041F2DA290311E682BCC5D1.xml new file mode 100644 index 00000000000..49a34cb71d8 --- /dev/null +++ b/data/38/68/F0/3868F0593041F2DA290311E682BCC5D1.xml @@ -0,0 +1,45 @@ + + + +Afrikanische Formiciden. + + + +Author + +Mayr, G. + +text + + +Annalen des Naturhistorischen Museums in Wien + + +1895 + +10 + + +124 +154 + + + + +http://antbase.org/ants/publications/4387/4387.pdf + +journal article +4387 + + + + +P. sulcata Andre +. + + + +Ein Weibchen aus Camerun (Dr. Brauns). + + + \ No newline at end of file diff --git a/data/38/69/09/386909486340846A7A70DE70050101E2.xml b/data/38/69/09/386909486340846A7A70DE70050101E2.xml new file mode 100644 index 00000000000..81a13e9b002 --- /dev/null +++ b/data/38/69/09/386909486340846A7A70DE70050101E2.xml @@ -0,0 +1,45 @@ + + + +New species of the catfish genus Trichomycterus (Siluriformes, Trichomycteridae) from the headwaters of the rio São Francisco basin, Brazil. + + + +Author + +Wolmar Benjamin Wosiacki + +text + + +Zootaxa + + +2004 + +592 + + +1 +12 + + + + +http://www.zoobank.org/urn:lsid:zoobank.org:pub:003431F8-DD57-4C9A-ACF9-B7F180E65729 + +journal article +z00592p001 +7907434C-6261-48ED-9034-27A3F4115F6E + + + + +T. unicolor + + + +ROM 51718 (3 ex.); + + + \ No newline at end of file diff --git a/data/38/69/09/386909BDAD77B91FB450D8C6C1F2A38C.xml b/data/38/69/09/386909BDAD77B91FB450D8C6C1F2A38C.xml new file mode 100644 index 00000000000..e3f025fc5ab --- /dev/null +++ b/data/38/69/09/386909BDAD77B91FB450D8C6C1F2A38C.xml @@ -0,0 +1,352 @@ + + + +Azooxanthellate Scleractinia (Cnidaria, Anthozoa) from South Africa + + + +Author + +Filander, Zoleka N. +https://orcid.org/0000-0002-6905-4440 +Biodiversity and Coastal Research, Oceans and Coasts, Department of Environment, Forestry, and Fisheries, Cape Town, South Africa & Zoology Department, Nelson Mandela University, Port Elizabeth, South Africa +zfilander@gmail.com + + + +Author + +Kitahara, Marcelo V. +Universidade Federal de Sao Paulo, Departamento de Ciencias do Mar, Santos, Brazil & Centro de Biologia Marinha, Universidade de Sao Paulo, Sao Sebastiao, Brazil + + + +Author + +Cairns, Stephen D. +Department of Invertebrate Zoology, Smithsonian Institution, Washington DC, USA + + + +Author + +Sink, Kerry J. +South African National Biodiversity Institute, Cape Town, South Africa & Institute for Coastal and Marine Research, Nelson Mandela University, Port Elizabeth, South Africa + + + +Author + +Lombard, Amanda T. +Institute for Coastal and Marine Research, Nelson Mandela University, Port Elizabeth, South Africa + +text + + +ZooKeys + + +2021 + +2021-10-28 + + +1066 + + +1 +198 + + + + +http://dx.doi.org/10.3897/zookeys.1066.69697 + +journal article +http://dx.doi.org/10.3897/zookeys.1066.69697 +1313-2970-1066-1 +133CE040A5AF44F1BC9A558C2F06A8AA +BD84F4C3157550C9B64120B2BE53F01A + + + + +Dendrophyllia ijimai Yabe & Eguchi, 1934 + + + + +Fig. 8O, P + + + + +Dendrophyllia ijimai +Yabe & Eguchi, 1934: 2026. - +Eguchi 1965a +: 294, 2 figs. - +Eguchi 1968 +: C65 (in part: pl. C16, figs 1, 2, pl. C22, fig. 1 +). -Kikuchi 1968 +: 9, pl. 15, fig. 2. - +Eguchi and Miyawaki 1975 +: 54. - +Cairns and Keller 1993 +: 280, fig. 13G +. -Cairns 1994 +: 89, pl. 38C, F. - +Cairns 1999a +: 133. - +Cairns et al. 1999 +: 26. - +Cairns 2001 +: 34 +. -Cairns 2004a +: 267, 315. - +Kitahara and Cairns 2021 +: 310, 312, figs 164, 165A-C. + + +Dendrophyllia micranthus +. - +Eguchi 1965a +: 294, fig. 1. - +Eguchi 1968 +: C66, pl. C24, figs 2, 3. + + +Dendrophyllia minuscula +. -van der +Horst 1922 +: 51-52, pl. 8, fig. 30 +. -Utinomi 1965 +: 257. - +Boshoff 1981 +: 42 +. -Tribble and Randall 1986 +: 159. + + +Dendrophyllia subcornigera cylindrica +Eguchi, 1968: C64-C65, pl. C32, figs 1, 2. + + +Dendrophyllia subcornigera +. - +Wells 1984 +: 215-216, fig. 5. + + +Dendrophyllia +sp. - +Zibrowius and Grygier 1985 +: 123, 126, figs 22, 23. + + +Dendrophyllia +sp. cf. +D. ijimai +. - +Cairns and Zibrowius 1997 +: 191-192, fig. 29E. + + + +Type locality. + +Presumably off Japan +(Cairns 1994 +). + + + +Type material. + +Presumably lost +(Cairns 1994 +). + + + +Material examined. + + +SAMC_A073008 ( +4 specimens +): +Eastern +margin, +33 km +from +Port Dunford +/ +38 km +off +Mlalazi Estuary +, +29°05'30.11"S +, +32°09'06.11"E +; + + +95 m + +. + + + +SAMC_A090121 ( +1 specimen +): +Eastern +margin, off +33 km +from +Port Dunford +/ +37 km +off +Mlalazi Estuary +, +29°08'59.99"S +, +32°05'24.00"E +; + + +85 m + +. + + + + +USNM 91843 ( +1 specimen +) + +: +Eastern +margin, +39 km +from +Cape Vidal +/ +29 km +off +Mgobezeleni Estuary +, +27°47'21.59"S +, +32°39'03.60"E +; + +62- +84 m. + + + + + +USNM 91844 ( +1 specimen +) + +: +Eastern +margin, +28 km +from + +Shaka's +Rock + +/ +19 km +off +Mdlotane Estuary +, +29°26'59.99"S +, +31°31'11.99"E +; + +68- +70 m. + + + + + + +Description. +Colony composed of one elongate, straight to slightly curved axial corallite, from which secondary corallites bud. Secondary corallites robust and bud in all directions, reaching ≤ 130 mm in H. Tertiary corallites small (<3 mm in H). Corallites circular to slightly elliptical (GCD:LCD = 1.0-1.1), with lanceted calicular margins Costae well defined, slightly ridged, and highly granular. Intercostal furrows deep and porous. Corallum white. + +Septa hexamerally arranged in four cycles, S5 occasionally present in some half-systems, in a strongly developed +Pourtales +plan according to the formula: S1 ≥ S2> S4> S3> S5 (≤ 60 septa). S1 independent and with straight axial margins. S2 as wide to only slightly smaller than S1, and have slightly sinuous axial margins. Both S1 and S2 extend to columella. S3 narrowest, also with slightly sinuous axial margins. S4 dimorphic in size, with laciniate axial margins: in half-systems without S5, S41/5 smaller than S2; however, in half-systems with S5, S4 half the size of S4. S4 arranged in +Pourtales +plan: curving towards common S3, and fusing before extending to columella as one septum. However, in half-systems with S5, the S5 is arranged in +Pourtales +plan: merging in front of flanked S4, before meandering towards S3 and joining S4 neighbouring S2. Septal faces finely granular. Fossa shallow to moderately deep, with a non-discrete spongy columella. + + + +Distribution. + +Regional: Eastern margin of South Africa, from off +Shaka's +Rock extending towards Cape Vidal; 62-95 m. Elsewhere: Japan (Yabe and +Eguchi 1934 +; Cairns 1994 +); Philippines; Indonesia ( +Cairns and Zibrowius 1997 +); Australia +(Cairns 2004a +); New Zealand; Red Sea +(Scheer and Pillai 1983 +); Zanzibar ( +Cairns and Keller 1993 +); 10-366 m. + + + +Remarks. + + +Dendrophyllia ijimai + +is the only + +Dendrophyllia + +species in the region that has arborescent colonies bearing large axial corallites that give off shorter corallites budding in an irregular form +(Cairns 1994 +). This growth form makes it easily distinguishable from the other South African congeners. Only one other western Pacific species is known to exhibit such a growth form ( + +D. cribrosa + +Milne-Edwards & Haime, 1851) and + +D. ijimai + +may be distinguished by its non-anastomotic branches (and exsert corallites) which are not flushed as in the case of + +D. cribrosa + +(see +Cairns 1994 +). As noted by +Cairns and Keller (1993) +, this species may be mistaken with + +Tubastraea micranthus + +, but differs in having its septa arranged in a well-developed +Pourtales +plan. + + + + \ No newline at end of file diff --git a/data/38/69/12/38691239AE5B6D00CFDF88AE6A02A592.xml b/data/38/69/12/38691239AE5B6D00CFDF88AE6A02A592.xml new file mode 100644 index 00000000000..7fa12f17626 --- /dev/null +++ b/data/38/69/12/38691239AE5B6D00CFDF88AE6A02A592.xml @@ -0,0 +1,49 @@ + + + +Études myrmécologiques en 1886. + + + +Author + +Forel, A. + +text + + +Annales de la Societe Entomologique de Belgique + + +1886 + +30 + + +131 +215 + + + + +http://antbase.org/ants/publications/3923/3923.pdf + +journal article +3923 +33E1E81D-6489-4D52-828D-DCA172BC7D97 + + + + +C. maculato-sylvaticus +; +C. maculato-cognatus + + +(= +variegatus Mayr +,; nec Smith). [Europe merid. et Afrique]. + + + + \ No newline at end of file diff --git a/data/38/69/59/386959B2018E41DA53B57DFA851975D7.xml b/data/38/69/59/386959B2018E41DA53B57DFA851975D7.xml new file mode 100644 index 00000000000..6338b025298 --- /dev/null +++ b/data/38/69/59/386959B2018E41DA53B57DFA851975D7.xml @@ -0,0 +1,129 @@ + + + +Revision of the family Chalcididae (Hymenoptera, Chalcidoidea) from Vietnam, with the description of 13 new species + + + +Author + +Narendran, T. C. + + + +Author + +van Achterberg, Cornelis + +text + + +ZooKeys + + +2016 + +576 + + +1 +202 + + + + +http://dx.doi.org/10.3897/zookeys.576.8177 + +journal article +http://dx.doi.org/10.3897/zookeys.576.8177 +1313-2970-576-1 +7A2FC762F23A4B138B0C0F1F80F46DA8 + + + +Taxon classification Animalia Hymenoptera Chalcididae + + + +Trigonura luzonensis Narendran, 1987 +Figs 200, 201 + + + + +Trigonura luzonensis +Narendran, 1987a: 288 (♀, Luzon, Philippines (USNM)), 1989: 216. + + + +Material. + +1 ♀ (RMNH), "S. Vietnam: +Dong +Nai, +Cat +Tien +N. P., c. 100 m, 1-9.x.2005, +Ficus +trail, Malaise traps 1-8, C. v. Achterberg & R. de Vries, +RMNH' +05. + + + +Diagnosis. + +This species resembles +Trigonura indica +Narendran in having the metasoma acuminate and oval and scutellum highly vaulted. However, +Trigonura luzonensis +differs from +Trigonura indica +in many features. In +Trigonura luzonensis +the outer disc of hind femur is densely and minutely punctate and blackish, without any yellow spot, whereas in +Trigonura indica +the punctures are less close on the hind femur and it is yellowish-red with a distinct characteristic yellow spot at the apex. The hind tibia is reddish-brown with its base black in +Trigonura indica +, whereas in +Trigonura luzonensis +the hind tibia is completely black. In addition, the punctation on T6 differs in both species. + + + +Description. +♀, length of body 6.2-7.0 mm. +Colour. Head black; eye and ocellus reflecting pale yellow; mandible rusty red except its black tips; mesosoma dorsally rusty-red and laterally and ventrally black; legs black with following parts rusty-red: tip of fore femur, base and tip of fore tibia, base and tip of mid tibia, hind coxa and all tarsi; fore wing slightly smoky. + +Head. Head with large close, umbilicate pits, interstices shorter than half diameter of a pit, rugose, almost carinate in most areas; POL 2.5-3.1 +x +OOL; interantennal projection in Vietnamese specimen reach just below anterior ocellus as a continuation of a carina from distal part of inter-antennal projection. + +Mesosoma. Pronotum with deep, close pits, interstices rugose-carinate; anterior margin of pronotum carinate laterally, posterior margin concave in middle; mesoscutum highly convex and vaulted with interstices between pits projecting as humps; scutellum highly convex and similarly sculptured. + +Wings +. Fore wing with PMV slightly longer than STV, 0.3 +x +as long as MV. + +Legs. Hind coxa densely punctate and pubescent on ventral side; hind femur with close minute setigerous pits, outer ventral margin with a row of irregular teeth, basal tooth much larger than others. + +Metasoma +. Metasoma with a small T1 (shorter than its width); metasoma a little longer than mesosoma. + +Male. Similar to ♀ except for stouter antenna and shorter metasoma. + + +Host. +Unknown. + + +Distribution. +Philippines, India, Vietnam (new record). + + +Variation. +The Vietnamese specimen has the dorsal part and distal ventral half of the hind coxa black and remaining baso-ventral part rusty red (Fig. 200). + + + \ No newline at end of file diff --git a/data/38/69/87/386987D1FFABFFF2B0CA83B5FC995032.xml b/data/38/69/87/386987D1FFABFFF2B0CA83B5FC995032.xml new file mode 100644 index 00000000000..8e9345727f3 --- /dev/null +++ b/data/38/69/87/386987D1FFABFFF2B0CA83B5FC995032.xml @@ -0,0 +1,80 @@ + + + +A phylogenetic study of the relationships within Mirinae subfamily (Insecta: Heteroptera: Miridae) based on specimens from Northern Iran: Insight into analyses of genera complexes + + + +Author + +Zamani, Mozhgan +0000-0003-2081-5285 +Department of Plant Protection, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran. P. O. Box: 41635 - 1314. & Mozhgan _ Zamani 90 @ yahoo. com; https: // orcid. org / 0000 - 0003 - 2081 - 5285 +amani90@yahoo.com + + + +Author + +Hosseini, Reza +Department of Plant Protection, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran. P. O. Box: 41635 - 1314. + +text + + +Zootaxa + + +2022 + +2022-10-27 + + +5200 + + +2 + + +101 +127 + + + +journal article +174101 +10.11646/zootaxa.5200.2.1 +10baad63-3710-4b0e-aff7-443ab3c87c03 +1175-5326 +7256717 +073A429D-3AA1-4B70-9E6E-56C6F282F47C + + + + + +Orthops + +genus + + + + +( +Fig. 2 +, node 8). + + + + +The genus + +Orthops + +has a worldwide distribution and includes 36 described species ( +Schuh 2002 +–2013). This clade is found to be monophyletic in maximum parsimony analyses with weak support (IW= 59%, EW= 55%). Morphological characters specific for this genus are male (such as the shape of left paramere and spicule) and female genitalia structures (such as interramal sclerites shape and distinctive form of dorsal structure in posterior wall of female genitalia). + + + + \ No newline at end of file diff --git a/data/38/69/87/386987D1FFABFFF2B0CA8519FE8A5256.xml b/data/38/69/87/386987D1FFABFFF2B0CA8519FE8A5256.xml new file mode 100644 index 00000000000..695b604dda4 --- /dev/null +++ b/data/38/69/87/386987D1FFABFFF2B0CA8519FE8A5256.xml @@ -0,0 +1,92 @@ + + + +A phylogenetic study of the relationships within Mirinae subfamily (Insecta: Heteroptera: Miridae) based on specimens from Northern Iran: Insight into analyses of genera complexes + + + +Author + +Zamani, Mozhgan +0000-0003-2081-5285 +Department of Plant Protection, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran. P. O. Box: 41635 - 1314. & Mozhgan _ Zamani 90 @ yahoo. com; https: // orcid. org / 0000 - 0003 - 2081 - 5285 +amani90@yahoo.com + + + +Author + +Hosseini, Reza +Department of Plant Protection, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran. P. O. Box: 41635 - 1314. + +text + + +Zootaxa + + +2022 + +2022-10-27 + + +5200 + + +2 + + +101 +127 + + + +journal article +174101 +10.11646/zootaxa.5200.2.1 +10baad63-3710-4b0e-aff7-443ab3c87c03 +1175-5326 +7256717 +073A429D-3AA1-4B70-9E6E-56C6F282F47C + + + + + +Polymerus + +genus + + + + +( +Fig. 2 +, node 6). + + + + +The genus comprises 99 species in the world ( +Schuh 2002 +–2013), which about 5 species have been reported and documented from +Iran +( +Aukema 2020 +). + +Polymerus + +is found to be a monophyletic group in all analyses with strong support (IW= 92%, EW= 86%). This genus is united with + +Eurystylus + +as a sister group in both analyses. The current result is congruent with previous studies ( +Jung & Lee 2012 +; +Kim & Jung 2019 +). + + + + \ No newline at end of file diff --git a/data/38/69/87/386987D1FFACFFF5B0CA8024FF7A51D2.xml b/data/38/69/87/386987D1FFACFFF5B0CA8024FF7A51D2.xml new file mode 100644 index 00000000000..04ffe8777d1 --- /dev/null +++ b/data/38/69/87/386987D1FFACFFF5B0CA8024FF7A51D2.xml @@ -0,0 +1,119 @@ + + + +A phylogenetic study of the relationships within Mirinae subfamily (Insecta: Heteroptera: Miridae) based on specimens from Northern Iran: Insight into analyses of genera complexes + + + +Author + +Zamani, Mozhgan +0000-0003-2081-5285 +Department of Plant Protection, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran. P. O. Box: 41635 - 1314. & Mozhgan _ Zamani 90 @ yahoo. com; https: // orcid. org / 0000 - 0003 - 2081 - 5285 +amani90@yahoo.com + + + +Author + +Hosseini, Reza +Department of Plant Protection, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran. P. O. Box: 41635 - 1314. + +text + + +Zootaxa + + +2022 + +2022-10-27 + + +5200 + + +2 + + +101 +127 + + + +journal article +174101 +10.11646/zootaxa.5200.2.1 +10baad63-3710-4b0e-aff7-443ab3c87c03 +1175-5326 +7256717 +073A429D-3AA1-4B70-9E6E-56C6F282F47C + + + + + +Grypocoris + +genus + + + + +( +Fig. 2 +, node 16). + + + + +Five species of + +Grypocoris + +are currently known in Palearctic region, which only + +G. fieberi + +and + +G. golestanicus + +are documented from +Iran +(occurrence of + +G. ajderensis +Putshkov, 1975 + +remains doubtful (see + +Aukema +et al +. 2013 + +; +Zamani & Hosseini 2018 +)). + +Grypocoris + +is a monophyletic group according to IW morphological analysis, with 61% support. This clade is supported by two synapomorphies: pretarsal with claw tooth (51-1) and pulvilli absent (53-0), and two other morphological characters including: shape of secondary gonopore (71-0) and sclerotized rings (79-1). In these analyses, genus + +Camponotidea + +( +Herdoniini +tribe) is united with + +Grypocoris + +as a sister group due to several morphological characters (e.g. size of eyes (12- 0) and position of metacoxae (46-1)). In the present study, the monophyly of + +Grypocoris + +is studied for the first time. + + + + \ No newline at end of file diff --git a/data/38/69/87/386987D1FFACFFF5B0CA83D9FC6B506A.xml b/data/38/69/87/386987D1FFACFFF5B0CA83D9FC6B506A.xml new file mode 100644 index 00000000000..351e951ba89 --- /dev/null +++ b/data/38/69/87/386987D1FFACFFF5B0CA83D9FC6B506A.xml @@ -0,0 +1,85 @@ + + + +A phylogenetic study of the relationships within Mirinae subfamily (Insecta: Heteroptera: Miridae) based on specimens from Northern Iran: Insight into analyses of genera complexes + + + +Author + +Zamani, Mozhgan +0000-0003-2081-5285 +Department of Plant Protection, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran. P. O. Box: 41635 - 1314. & Mozhgan _ Zamani 90 @ yahoo. com; https: // orcid. org / 0000 - 0003 - 2081 - 5285 +amani90@yahoo.com + + + +Author + +Hosseini, Reza +Department of Plant Protection, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran. P. O. Box: 41635 - 1314. + +text + + +Zootaxa + + +2022 + +2022-10-27 + + +5200 + + +2 + + +101 +127 + + + +journal article +174101 +10.11646/zootaxa.5200.2.1 +10baad63-3710-4b0e-aff7-443ab3c87c03 +1175-5326 +7256717 +073A429D-3AA1-4B70-9E6E-56C6F282F47C + + + + + +Adelphocoris + +genus + + + + +( +Fig. 2 +, node 15). + + + + + +Adelphocoris + +comprises 48 species in the world and most of them occur in the Palearctic region ( +Schuh 2002 +–2013). Hitherto six species have been reported from +Iran +(Ghahari & Charot 2014). This genus is a monophyletic group according to all analyses with strong support (IW= 83%, EW= 73%). This genus is united with + +Creontiades + +as a sister group in both analyses. + + + + \ No newline at end of file diff --git a/data/38/69/87/386987D1FFACFFF5B0CA85D1FD5B523A.xml b/data/38/69/87/386987D1FFACFFF5B0CA85D1FD5B523A.xml new file mode 100644 index 00000000000..6f09fae9215 --- /dev/null +++ b/data/38/69/87/386987D1FFACFFF5B0CA85D1FD5B523A.xml @@ -0,0 +1,88 @@ + + + +A phylogenetic study of the relationships within Mirinae subfamily (Insecta: Heteroptera: Miridae) based on specimens from Northern Iran: Insight into analyses of genera complexes + + + +Author + +Zamani, Mozhgan +0000-0003-2081-5285 +Department of Plant Protection, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran. P. O. Box: 41635 - 1314. & Mozhgan _ Zamani 90 @ yahoo. com; https: // orcid. org / 0000 - 0003 - 2081 - 5285 +amani90@yahoo.com + + + +Author + +Hosseini, Reza +Department of Plant Protection, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran. P. O. Box: 41635 - 1314. + +text + + +Zootaxa + + +2022 + +2022-10-27 + + +5200 + + +2 + + +101 +127 + + + +journal article +174101 +10.11646/zootaxa.5200.2.1 +10baad63-3710-4b0e-aff7-443ab3c87c03 +1175-5326 +7256717 +073A429D-3AA1-4B70-9E6E-56C6F282F47C + + + + + +Phytocoris + +genus + + + + +( +Fig. 2 +, node 13). + + + + +The genus comprises 275 species known from the Palearctic region, which about 62 species have been reported and documented from +Iran +( +Hosseini & Mohammadi 2018 +, 2019; +Zamani & Hosseini 2019 +; +Aukema 2020 +). + +Phytocoris + +is recovered as a monophyletic group in both analyses, by 70% resampling support. This result is congruent with Kim & Jung’s phylogenetic analyses based on total evidence ( +Kim & Jung 2019 +). Morphological characters supporting this clade include: antenna longer than body (16-1) and hind femora narrowed towards apex (48-2). + + + + \ No newline at end of file diff --git a/data/38/69/87/386987D1FFACFFF5B0CA87A4FDBC54EE.xml b/data/38/69/87/386987D1FFACFFF5B0CA87A4FDBC54EE.xml new file mode 100644 index 00000000000..0b11580a141 --- /dev/null +++ b/data/38/69/87/386987D1FFACFFF5B0CA87A4FDBC54EE.xml @@ -0,0 +1,102 @@ + + + +A phylogenetic study of the relationships within Mirinae subfamily (Insecta: Heteroptera: Miridae) based on specimens from Northern Iran: Insight into analyses of genera complexes + + + +Author + +Zamani, Mozhgan +0000-0003-2081-5285 +Department of Plant Protection, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran. P. O. Box: 41635 - 1314. & Mozhgan _ Zamani 90 @ yahoo. com; https: // orcid. org / 0000 - 0003 - 2081 - 5285 +amani90@yahoo.com + + + +Author + +Hosseini, Reza +Department of Plant Protection, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran. P. O. Box: 41635 - 1314. + +text + + +Zootaxa + + +2022 + +2022-10-27 + + +5200 + + +2 + + +101 +127 + + + +journal article +174101 +10.11646/zootaxa.5200.2.1 +10baad63-3710-4b0e-aff7-443ab3c87c03 +1175-5326 +7256717 +073A429D-3AA1-4B70-9E6E-56C6F282F47C + + + + + +Lygus + +genus + + + + +( +Fig. 2 +, node 11). + + + + + +Lygus +species + +are economically important group of insects in many agro-ecosystems ( + +Shrestha +et al +. 2007 + +). This genus comprises 163 species in the world ( +Schuh 2002 +–2013), where three species have been recorded from +Iran +( +Aukema 2020 +). The genus + +Lygus + +was recovered as a monophyletic group according to all analyses, with strong support (IW= 88%, EW= 86%). The monophyly of the genus + +Lygus + +was found in the previous studies based on morphological, molecular and combine data sets (e.g., +Schwartz & Foottit 1998 +; +Kim & Jung 2019 +). + + + + \ No newline at end of file diff --git a/data/38/69/87/386987D1FFADFFF4B0CA8781FCBF54B6.xml b/data/38/69/87/386987D1FFADFFF4B0CA8781FCBF54B6.xml new file mode 100644 index 00000000000..a456d20fc68 --- /dev/null +++ b/data/38/69/87/386987D1FFADFFF4B0CA8781FCBF54B6.xml @@ -0,0 +1,86 @@ + + + +A phylogenetic study of the relationships within Mirinae subfamily (Insecta: Heteroptera: Miridae) based on specimens from Northern Iran: Insight into analyses of genera complexes + + + +Author + +Zamani, Mozhgan +0000-0003-2081-5285 +Department of Plant Protection, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran. P. O. Box: 41635 - 1314. & Mozhgan _ Zamani 90 @ yahoo. com; https: // orcid. org / 0000 - 0003 - 2081 - 5285 +amani90@yahoo.com + + + +Author + +Hosseini, Reza +Department of Plant Protection, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran. P. O. Box: 41635 - 1314. + +text + + +Zootaxa + + +2022 + +2022-10-27 + + +5200 + + +2 + + +101 +127 + + + +journal article +174101 +10.11646/zootaxa.5200.2.1 +10baad63-3710-4b0e-aff7-443ab3c87c03 +1175-5326 +7256717 +073A429D-3AA1-4B70-9E6E-56C6F282F47C + + + + + +Brachycoleus + +genus + + + + +( +Fig. 2 +, node 18). + + + + +The genus comprises ten species known from the Palearctic region (Hosseini & Mohammadi 2019, +Aukema 2020 +) with four species reported from +Iran +. + +Brachycoleus + +is found to be monophyletic in both analyses with moderate support (IW= 62%, EW= 66%). This clade is supported by a unique synapomorphy (20-0) and four other morphological characters including: swollen frons (7-1), left paramere apophysis, subapically expanded (58-1), median process of posterior wall present/small (86-1) and dorsal margin of second valvula edentate or ventral margin moderately dentate (89-0). In the present study, the monophyly of + +Brachycoleus + +is studied for the first time. + + + + \ No newline at end of file diff --git a/data/38/69/C7/3869C7825F6ED001AD8B1AC2CCFA93E2.xml b/data/38/69/C7/3869C7825F6ED001AD8B1AC2CCFA93E2.xml new file mode 100644 index 00000000000..22cf1ad3f8a --- /dev/null +++ b/data/38/69/C7/3869C7825F6ED001AD8B1AC2CCFA93E2.xml @@ -0,0 +1,47 @@ + + + +H. Sauter's Formosa-Ausbeute: Formicidae (Hym.). + + + +Author + +Forel, A. + +text + + +Entomologische Mitteilungen + + +1912 + +1 + + +45 +81 + + + + +http://antbase.org/ants/publications/4035/4035.pdf + +journal article +4035 + + + + +Vollenhovia Emeryi Wheeler + + + +[[worker]]. Darunter ein kleines, 2,3 mm anges ergatomorphes [[queen]] (kleines, aber doch [[queen]] aehnliches Mesonotum). + + +Pilam. + + + \ No newline at end of file diff --git a/data/38/6A/87/386A87B5FFE7266F75C9FE35FB7AFE37.xml b/data/38/6A/87/386A87B5FFE7266F75C9FE35FB7AFE37.xml new file mode 100644 index 00000000000..db13eedb353 --- /dev/null +++ b/data/38/6A/87/386A87B5FFE7266F75C9FE35FB7AFE37.xml @@ -0,0 +1,622 @@ + + + +Crocidura hikmiya, a new shrew (Mammalia: Soricomorpha: Soricidae) from Sri Lanka + + + +Author + +Meegaskumbura, Suyama + + + +Author + +Meegaskumbura, Madhava + + + +Author + +Pethiyagoda, Rohan + + + +Author + +Manamendra-Arachchi, Kelum + + + +Author + +Schneider, Christopher J. + +text + + +Zootaxa + + +2007 + +1665 + + +19 +30 + + + +journal article +10.5281/zenodo.180054 +ec3c5a27-2388-4f0a-bbfa-e43ef1015717 +1175-5326 +180054 + + + + + + + +Crocidura hikmiya + +sp. nov. +( +Fig. 2 +) + + + + + + + +Holotype +. + +WHT 6845 (male, 76.0 mm HBL, +7.8 g +mass in life), preserved in alcohol; skull removed and preserved separately. Collected by M. Meegaskumbura and M. Bahir on +25 January 2004 +, at Kudawa, Sinharaja Forest Reserve ( +06°26’N +, +80°25’E +, elevation +460 m +). + + + +Paratypes +. + +WHT 6836 (male, 64.0 mm HBL), WHT 6837 (female, 73.0 mm HBL), WHT 6843 (female, +69.9 mm +HBL), and WHT 6844 (female, 71.0 mm HBL), collected from +20 – 25 January 2004 +, other collection data same as +holotype +. WHT 6849 (male, +62.5 mm +HBL) and WHT 6853 (male, +67.1 mm +HBL), collected by M. Meegaskumbura and K. Manamendra-Arachchi from +31 January- 4 February 2004 +at Morningside ( +06°24.36’N +, +80°86.87’E +, elevation +1040 m +). All specimens preserved in alcohol; skulls removed and preserved separately. + + + + +Etymology. +The specific epithet ‘hikmiya’ is Sinhala for ‘shrew’, applied here as a substantive in apposition. + + + + +Diagnosis. + +Crocidura hikmiya + +is distinguished from + +C. miya +, + +its sister-species (see +Fig. 3 +and below), by the following external characters ( +Table 1 +) and cranial characters ( +Table 2 +): shorter tail length 101.4–114.5% of HBL ( +vs +135.0–154.6% of HBL in + +C. miya + +); longer forefeet, +9.3–10.2 mm +( +vs. +8.7–9.0 mm in + +C. miya + +); a narrower least inter-orbital breadth +3.9–4.2 mm +( +vs. +4.2–4.4 mm +in + +C. miya + +); broader breadth of rostrum at narrowest point, +1.9–2.2 mm +( +vs. +1.8–1.9 mm +in + +C. miya + +); occipital condyles protrude beyond braincase ( +vs. +condyles do not protrude beyond braincase in + +C. miya + +); posterior edge of maxillary bone rounded ( +vs. +triangular in + +C. miya + +); in dorsal view the occipital bone is triangular shaped with an obtuse angle ( +vs. +acute angle in + +C. miya + +); occipital bone is slightly flattened on the back ( +vs. +rounded in + +C. miya + +); in ventral view foramen magnum less deep ( +vs. +deep in + +C. miya + +); dorsal posterior brain case is not smooth ( +vs. +smooth in + +C. miya + +); angular process of dentary short and stout ( +vs. +long and thin in + +C. miya + +) ( +Fig. 4 +). The two species also differ in coloration, + +C. hikmiya + +is dark grey-brown on the dorsum including the tail and slightly lighter colored on ventral surface of body and tail ( + +vs. +C. miya + +which is brown on the dorsum including the tail and slightly lighter colored ventrally). There are no differences in the tooth characteristics between the two species. + + + + +Description. + +Crocidura hikmiya + +is a medium-sized shrew with a +64–76 mm +HBL in the +type +series, which comprises sexually mature individuals. Tail slender, its length slightly exceeding that of head and body (tail length 101.4–114.5% of HBL) (see +Table 1 +), semi-naked, with long, protruding hairs extending along proximal 13–24% of its length. Head length +26.2–28.9 mm +(36.0–43.1% of HBL). Ears prominent, naked, height 7.0– +8.9 mm +. Snout pink, with long bristles interspersed among shorter ones; bristles dark at base, paling to silvery grey at tips. Eyes small (< +1 mm +in diameter, measured horizontally). General color of body including tail dark grey-brown. Venter slightly lighter colored than dorsum. Several long, dark, ‘guard hairs’ interspersed among grey hairs on both dorsal and ventral sides of body; individual hairs grey at base, with brown tips. Dorsal side of hands and feet semi-naked, appearing pinkish brown, with sparse brown hairs on digits. + + +External and cranial measurements (mm) of the +holotype +of + +C. hikmiya + +(WHT 6845): HBL, 76.0; HL, 27.8; TL, 77.5; HFL, 17.0; TBL, 19.7; FFL, 9.5; LAL, 12.4; EH, 8.9; GL, 20.2; BL, 18.2; BAL, 17.1; CL, 20.2; MTR, 6.0; PL, 8.8; PAL, 7.9; PPL, 9.8; LR, 7.1; BB, 9.0; LIOB, 4.2; PW1, 5.9; PW2, 3.1; BR1, 2.2; BR2, 6.1; BPM, 1.6; BMM, 1.0; HB, 5.2; ML, 11.4; LDI, 13.0; LDT1, 6.1; LDT2, 8.3; DD, 5.5. + + + + +FIGURE 2. +In-vivo +portrait of + +Crocidura hikmiya + +paratype, WHT 6849, male, 62.5 mm HBL. + + + + +FIGURE 3. +Phylogram inferred from Bayesian analysis of combined cytochrome +b ++ 16S data sets under model GTR+I+G. Posterior probability and bootstrap values (expressed as percentages) are given above and below branches, respectively. + + + + +TABLE 2. +Skull measurements of + +C. hikmiya + +and + +C. miya +. + +Refer to Materials and Methods for abbreviations. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+ +C. hikmiya + + + +C. miya + +
RangeMean (SD)RangeMean (SD)
GL19.2–20.219.7 (0.3)19.5–20.720.1 (0.5)
BL17.3–18.217.6 (0.3)17.3–18.017.6 (0.3)
BSL16.1–17.316.7 (0.4)16.4–17.216.8 (0.3)
CL19.2–20.219.7 (0.3)19.6–20.319.9 (0.3)
MTR5.6–6.15.8 (0.2)5.6–5.85.7 (0.1)
PL8.3–8.88.6 (0.2)7.9–8.48.1 (0.2)
PAL7.2–7.97.5 (0.2)7.1–7.67.4 (0.2)
PPL9.2–9.89.5 (0.2)9.2–10.19.7 (0.4)
LR6.9–7.17.0 (0.1)6.8–7.37.0 (0.2)
BB8.9–9.09.0 (0.1)8.9–9.29.1 (0.1)
LIOB3.9–4.24.1 (0.1)4.2–4.44.3 (0.1)
PW15.5–5.95.7 (0.2)5.7–5.95.8 (0.1)
PW22.6–3.12.8 (0.2)2.7–2.92.8 (0.1)
BR11.9–2.22.0 (0.1)1.8–1.91.9 (0.1)
BR25.9–6.26.1 (0.1)6.0–6.26.1 (0.1)
BPM1.4–1.61.5 (0.1)1.4–1.61.6 (0.1)
BMM1.0–1.11.0 (0.0)0.9–1.11.0 (0.1)
HB4.8–5.24.9 (0.1)4.9–5.25.1 (0.1)
ML10.8–11.411.1 (0.2)10.5–11.010.8 (0.2)
LDI12.4–13.112.8 (0.2)12.2–12.912.5 (0.3)
LDT16.0–6.26.1 (0.1)6.0–6.36.1 (0.1)
LDT28.0–8.38.1 (0.2)7.9–8.38.1 (0.2)
DD5.2–5.65.4 (0.1)5.0–5.45.2 (0.2)
+
+ + +Distribution. + +Crocidura hikmiya + +is known only from two forest-edge sites in Sinharaja Forest, at Kudawa and Morningside. + + + + +Variation. +There is no apparent sexual dimorphism among the specimens collected. All specimens from both sites were of approximately the same size (mean mass = 7.7; SD = 1.0); however, both ventral and dorsal colors of the Morningside specimens were comparatively lighter than those from Kudawa. One specimen (WHT 6837) has 5 unicuspid teeth on each side of upper jaw instead of 3, as observed in all other specimens of + +C. hikmiya + +: the first of these is located immediately posterior to the first incisor, having thrusted the latter forwards and upwards. It has also displaced the tooth immediately posterior to it. The first incisor of this specimen is +0.2 mm +smaller than the first incisor in other specimens. This ‘extra’ tooth is triangular in buccal and occlusal views and the pointed end protrudes towards the palate in occlusal view. The second ‘extra’ tooth is small, triangular in occlusal view and located at the end of the unicuspid tooth row filling the space between the other unicuspids and the pre-molar. Due to the addition of ‘extra’ unicuspid teeth, the length of unicuspid tooth-row has increased by +0.2–0.4 mm +than other normal specimens. However, due to the smaller size of the first incisor and displaced unicuspid tooth posterior to the first ‘extra’ tooth, the upper jaw tooth row remains the same length as that of other specimens ( +Fig. 5 +). + + +Phylogenetic analysis. +Both Bayesian and maximum parsimony phylogenetic trees based on mitochondrial DNA sequence data strongly supports + +C. hikmiya + +as the sister species of + +C. miya + +( +Fig. 3 +). The Bayesian percentage posterior probability of the clade that includes only + +C. miya + +and + +C. hikmiya + +is 100, and the nonparametric parsimony bootstrap value for the same clade is 71% ( +Fig. 3 +). The percent pairwise uncorrected distance between these two species for the cytochrome- +b +gene fragment is 9.7–10.1%, while that between the currently-recognized species + +C. miya + +and + +C. horsfieldii + +is 11.5–11.6%; the latter, however, are not sister species. The percent pairwise uncorrected distance between + +C. hikmiya + +and + +C. horsfieldii + +is 13.3–13.6. + + +Morphological analysis. +Principal Components Analysis of external measurements revealed that + +C. hikmiya + +and + +C. miya + +differ in multivariate morphological space along a single axis that represents tail length and forefoot length. PCA of the correlation matrix among variables resulted in four axes that explained a total of 88.7% of the total variance. Factor scores for + +C. hikmiya + +and + +C. miya + +overlap substantially on PC2, PC3, and PC4, but differ on PC1 ( +Fig. 6 +A). PC1 explained 31.8% of the variance in external morphological variables. Tail length loaded heavily and positively on PC1, whereas forefoot length had a high negative loading. Factor scores from the two species do not overlap on PC1, with + +C. hikmiya + +having shorter tail and longer forefoot, and + +C. miya + +having longer tail and shorter forefoot. + + + +FIGURE 4. +Dorsal, ventral and lateral views of crania (and mandibule in the latter case) of + +Crocidura hikmiya + +: WHT6845 (A–D) and + +C. miya + +WHT6826 (E–H). Arrows indicate skull characteristics that are different between the two species. + + + +PCA of cranial variables revealed that + +C. hikmiya + +and + +C. miya + +differed primarily on PC2, with substantial overlap of factor scores on PC1 ( +Fig. 6 +B). PC1, which explained 33.6% of the variation, is largely a size axis, with high positive loadings for linear measurements reflecting skull dimensions (Basal Length, Mandible Length and Dentary Length Excluding Incisors). The two species overlapped substantially on PC1 indicating little variation in overall size. PC2 explained 20.1% of the total variance and had high positive loadings for Least Interorbital Breadth and Breadth of Braincase and high negative loading for breadth of rostrum at narrowest point and palatal length. Factor scores of the two species do not overlap on PC2, with + +C. hikmiya + +having a narrower least interorbital breadth, narrower breadth of braincase on average, broader breadth of rostrum at narrowest point and longer palatal length on average than + +C. miya + +( +Fig. 4 +; +Table 2 +). PC3 and PC4 explained 13.5% and 12.3% of the total variance respectively, but factor scores of the two species overlap completely on these axes (plots not shown). These analyses indicate that + +C. hikmiya + +and + +C. miya + +occupy different regions of morphospace for both cranial and external features and are diagnosable morphologically. + +In addition, several characteristics of the skull also diagnose the species (see Diagnosis). + +
+
\ No newline at end of file diff --git a/data/38/6A/B8/386AB8BEDBF62257883F41DBF8B888D8.xml b/data/38/6A/B8/386AB8BEDBF62257883F41DBF8B888D8.xml new file mode 100644 index 00000000000..d9b78a870ef --- /dev/null +++ b/data/38/6A/B8/386AB8BEDBF62257883F41DBF8B888D8.xml @@ -0,0 +1,76 @@ + + + +Checklist of British and Irish Hymenoptera - Sawflies, ' Symphyta' + + + +Author + +Liston, Andrew D. + + + +Author + +Knight, Guy T. + + + +Author + +Sheppard, David A. + + + +Author + +Broad, Gavin R. + + + +Author + +Livermore, Laurence + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1168 +1168 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1168 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1168 +1314-2828-2-1168 + + + + +Arge Schrank, 1802 + + + + +CRYPTUS +Jurine, 1801 suppressed + + +HYLOTOMA +Latreille, 1802 + + + + \ No newline at end of file diff --git a/data/38/6A/BE/386ABE42FFA0FFBCFF06AD0B2F63F9AC.xml b/data/38/6A/BE/386ABE42FFA0FFBCFF06AD0B2F63F9AC.xml new file mode 100644 index 00000000000..a2909d929b9 --- /dev/null +++ b/data/38/6A/BE/386ABE42FFA0FFBCFF06AD0B2F63F9AC.xml @@ -0,0 +1,586 @@ + + + +Alpheid shrimps of the genera Athanas Leach, 1814, Athanopsis Coutière, 1897 and Pseudathanas Bruce, 1983 of the coasts of the Arabian Peninsula (Malacostraca: Decapoda: Caridea) + + + +Author + +Anker, Arthur +Universidade Federal de Pelotas (UFPEL), Departamento de Ecologia, Zoologia e Genética, Instituto de Biologia, Campus Universitário Capão do Leão, RS, 96010 - 610, Brazil & Red Sea Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia + +text + + +Zootaxa + + +2023 + +2023-12-11 + + +5383 + + +2 + + +179 +215 + + + + +https://www.mapress.com/zt/article/download/zootaxa.5383.2.5/52448 + +journal article +10.11646/zootaxa.5383.2.5 +1175-5326 +10350767 +7E434B40-6346-4E6D-BC55-38EBAE24BD52 + + + + + + + +Athanopsis brevirostris +Banner & Banner, 1981 + + + + + + + +( +Fig. 8a, b +) + + + + + + + +Athanopsis brevirostris +Banner & Banner 1981: 45 + + +, fig. 5; + +Anker 2012: 51 + +, figs. 2–4, 7A, B. + + + + + +Material examined +. 1 ovig. female (cl 5.0 mm), +FLMNH +UF +71444, +Saudi Arabia +, Thuwal, near +KAUST +King Abdullah Monument, +22°20’26.2”N +/ +39°05’15.1”E +, shallow subtidal sandflat with seagrass and rubble patches, depth +0.5–1.5 m +, suction pump, in echiuran burrow, leg. A. Anker, +20.01.2023 +[fcn AA-22-497]; + +1 male +(cl +4.1 mm +), 1 ovig. female (cl +4.4 mm +), +FLMNH +UF 71426 +, same collection data as for previous specimen [fcn AA-22-474] + +; + +1 male +(cl +3.6 mm +), +FLMNH +IUF 71429 +, same collection data as for previous specimens [fcn AA-22-489] + +; + +1 male +(cl +3.9 mm +), +FLMNH +UF 71441 +, same collection data as for previous specimens [fcn AA-22-467]; 1 ovig. female (cl +4.4 mm +), +FLMNH +UF 71442 +, same collection locality as for previous specimens, leg. +A. Anker +, + +21.01.2023 + +[fcn AA-22-500] + +; + +1 male +(cl +4.4 mm +), +FLMNH +UF 71427 +, same collection data as for previous specimen [fcn AA-22-511] + +; + +1 female +(cl ~ +3.5 mm +), +FLMNH +UF 36637 +, +Saudi Arabia +, +Farasan Islands +, +Marca Island +, +18°13’14.0”N +/ +41°19’27.8”E +, subtidal sandflat, depth + +5–10 m + +, suction pump, in burrow of unknown host, leg. +A. Anker +et al +., + +06.03.2013 + +[fcn BDJRS-1756] + +. + + +Comparative material +. + +Athanopsis saurus +Anker, 2011: + +1 + + +female (cl +3.6 mm +), MNHN-2018-571, +New Caledonia +, +Koumac +, +Pointe Pandop +, +Expedition Koumac +2.1 sta. +KM601 +, +20°35’S +/ +164°16.5’E +, partly exposed sand-mud intertidal with coral rubble fragments, depth + +0–0.2 m + +, suction pump, in echiuran burrow, leg. +A. Anker +, + +08.09.2018 + +; + +1 female +(cl 5.0 mm), MNHN-2018-1012, +New Caledonia +, +Saint-Mathieu +, +Expedition Koumac +2.1 +Miscellanea +sta. +KM606 +, +20°22.8’S +/ +164°35’E +, shallow sandflat with sparse seagrass near +Pouébo river +estuary and mangroves, depth + +0–0.5 m + +, suction pump, in echiuran burrow, leg. +A. Anker +& +Z. Ďuriš +, + +18.09.2018 + + +; + +1 ovig. female (cl +4.9 mm +), MNHN-2018-978, same collection data as for previous specimen + +; + +1 male +(cl +4.3 mm +), MNHN- IU-2018-974, same collection data as for previous specimens + +. + + + + +Description +. See +Banner & Banner (1981) +for original description and illustrations, and +Anker (2012) +for additional illustrations of the Madagascan material; colour pattern of the Saudi Arabian specimens is shown in +Fig. 8a, b +. + + +Colour in life +. Described in detail in +Anker (2012: 53 +, fig. 7A, B); see also +Fig. 8a, b +. + + + + +Distribution +. +Red Sea +: +Eritrea +: Dahlak Archipelago ( +Banner & Banner 1981 +), +Saudi Arabia +: Thuwal, Farasan Islands (present study); +Madagascar +: Nosy-Bé; +Japan +: +Okinawa +( +Anker 2012 +). + + + + +FIGURE 8. + +Athanopsis brevirostris +Banner & Banner, 1981 + +, ovigerous female (cl 5.0 mm) from Thuwal, Saudi Arabia (FLMNH UF 71444) [a, b] and its host [c]; a, shrimp in life, lateral (right side); b, same, dorsal; c, burrowing echiuran, probably + +Ochetostoma +sp. + +or + +Listriolobus +sp. + +( +Thalassematidae +), photographed shortly after death. Photographs by the author. + + + + +FIGURE 9. + +Athanopsis saurus +Anker, 2011 + +, male (cl 4.3 mm) from Pouébo, New Caledonia (MNHN-IU-2018-974) [a–e] and its host [f]; a, shrimp in life, lateral (left side); b, same, dorsal; c, d, e, shrimp on various areas of the host (see f); f, burrowing echiuran, probably + +Ochetostoma +sp. + +( +Thalassematidae +), with commensal bivalves attached to the trunk (two of them also visible in c). Photographs by the author. + + + + +Ecology +. Most Saudi Arabian specimens of + +A. brevirostris + +were collected together with echiuran hosts, a large reddish species possibly belonging to either the genus + +Ochetostoma +Rüppel & Leuckart + +or the related genus + +Listriolobus +Fischer + +( +Thalassematidae +) ( +Fig. 8c +). Some of the previously reported specimens of + +A. brevirostris + +were also extracted from burrows of + +Ochetostoma +sp. + +or unknown hosts, however, the +holotype +came from a poisoning station ( +Banner & Banner 1981 +; +Anker 2012 +). Thus, the present evidence suggests that all species of + +Athanopsis + +live in symbiosis with echiurans ( +Miya 1980 +; +Berggren 1991 +; Anker 2011, 2012; + +Marin +et al +. 2014 + +; present study). + + + + +Remarks +. +Anker (2012) +separated + +A. brevirostris + +from the closely related + +A. saurus + +(type locality: Lizard Island, Great Barrier Reef) by the following four features: (1) rostrum short, with lateral margins broadly concave in + +A. brevirostris +vs. + +longer, with lateral margins proximally convex in + +A. saurus + +; (2) second antennular peduncle much wider than long in + +A. brevirostris +vs. + +only slightly wider than long (almost square-shaped) in + +A. saurus + +; (3) major chela palm with small field of setae distally in + +A. brevirostris +vs. + +with more extensive setation in + +A. saurus + +; and (4) colour pattern with more white on the second and third pleonites and less red on the carapace in + +A. saurus + +. As pointed out by +Anker (2012) +, in the +holotype +of + +A. brevirostris + +, as well as in the Madagascan material assigned to that species, the merus of the third to fifth pereiopods has a small distolateral tooth, which was not overlooked by +Banner & Banner (1981) +; this tooth is present, and sometimes quite conspicuous, in all Saudi Arabian specimens. + + +The New Caledonian material is morphologically somewhat intermediate between + +A. brevirostris + +and + +A. saurus + +, especially in the features of the rostrum and major chela, raising at least the possibility that the two species may be synonymous. Indeed, the aforementioned morphological differences between + +A. brevirostris + +and + +A. saurus + +are slight and somewhat subjective, and need to be verified when more material becomes available. In addition, the colour pattern of the Saudi Arabian specimens of + +A. brevirostris + +( +Fig. 8a, b +) appears to be closer to the pattern of + +A. saurus + +from Lizard Island (Anker 2011: fig. 8G, H; +Anker 2012 +: fig. 7E), whereas the colour pattern of the Madagascan specimens reported as + +A. brevirostris + +( +Anker 2012 +: fig. 7A, B) is very similar to that of the New Caledonian specimens herein identified as + +A. saurus + +( +Fig. 9a–e +). Thus, the present material largely eliminates the colour differences between the two species listed by +Anker (2012) +. Nonetheless, while contrasting published colour photographs of + +A. brevirostris + +and + +A. saurus + +(Anker 2011, 2012) with those available for the present material ( +Figs. 8 +, +9 +), the author noticed one colour difference that could reveal as diagnostic. In the shrimps identified as + +A. brevirostris + +from the Red Sea (Farasan Islands, Thuwal), +Madagascar +(Nosy Bé), and +Japan +( +Okinawa +), the carapace is typically white or white locally speckled with small red chromatophores, especially on the anterolateral surface ( +Fig. 8a +; +Anker 2012 +: fig. 7A, B; +Goto & Kato 2012 +: fig. 1h). In the +holotype +of + +A. saurus + +from +Australia +(Lizard Island) and specimens from +New Caledonia +(Koumac, Pouébo) herein identified as + +A. saurus + +, the carapace is white with large patches of red chromatophores on the anterolateral surface ( +Fig. 9a, d +; Anker 2011: fig. 8G; +Anker 2012 +: fig. 7E). It also appears that the red patches on the pleon of + +A. saurus + +extend to additional pleonites. Importantly, + +A. brevirostris + +and + +A. saurus + +were recovered as sister species in the molecular phylogeny of + +Chow +et al. +(2021 + +: fig. 3), where the former was represented by a specimen from Okinawa (listed in +Anker 2012 +), and the latter by a specimen from +New Caledonia +(MNHN-IU-2018-978). The genetic distance between them was not significant, but sufficient to be considered as interspecific (3.1% for 16S; genetic distance presently unavailable for COI). The next step would be to compare sequences from the +holotype +of + +A. saurus + +and the western Indian Ocean (Red Sea, +Madagascar +) material of + +A. brevirostris + +, to draw the final conclusion about the taxonomic status of the former species. + + + + \ No newline at end of file diff --git a/data/38/6A/BE/386ABE42FFA3FFB7FF06A8172F57F878.xml b/data/38/6A/BE/386ABE42FFA3FFB7FF06A8172F57F878.xml new file mode 100644 index 00000000000..f1816030ac6 --- /dev/null +++ b/data/38/6A/BE/386ABE42FFA3FFB7FF06A8172F57F878.xml @@ -0,0 +1,618 @@ + + + +Alpheid shrimps of the genera Athanas Leach, 1814, Athanopsis Coutière, 1897 and Pseudathanas Bruce, 1983 of the coasts of the Arabian Peninsula (Malacostraca: Decapoda: Caridea) + + + +Author + +Anker, Arthur +Universidade Federal de Pelotas (UFPEL), Departamento de Ecologia, Zoologia e Genética, Instituto de Biologia, Campus Universitário Capão do Leão, RS, 96010 - 610, Brazil & Red Sea Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia + +text + + +Zootaxa + + +2023 + +2023-12-11 + + +5383 + + +2 + + +179 +215 + + + + +https://www.mapress.com/zt/article/download/zootaxa.5383.2.5/52448 + +journal article +10.11646/zootaxa.5383.2.5 +1175-5326 +10350767 +7E434B40-6346-4E6D-BC55-38EBAE24BD52 + + + + + + + +Athanopsis dawa + +sp. nov. + + + + + + +( +Figs. 10 +, +11 +, +12a, b +) + + + + +Material examined +. + +Holotype +: ovig. female (cl +4.4 mm +), +FLMNH +UF 71424 +, +Oman +, +Masirah Island +, channel side, +Dafiyat +, +20°35’15.1”N +/ +58°49’36.9”E +, intertidal and shallow subtidal sandflat with patches of coral rubble, rocks and seagrass, depth at low tide + +0.1–0.5 m + +, suction pump, in echiuran burrow, leg. +A. Anker +, + +07.11.2022 + +[fcn BOMAN-13017] + +. + +Paratype +: ovig. female (cl +4.7 mm +), +FLMNH +UF 71423 +, same collection data as for holotype [fcn BOMAN-13028] + +. + + + + +Description +. Carapace ( +Fig.10a–d +) glabrous, somewhat domed, with conspicuous, anteriorly directed postrostral tubercle. Rostrum ( +Fig. 10b, c, d +) moderately long, overreaching distal margin of first article of antennular peduncle, subtriangular, as long as broad at base, with acute tip; rostral carina distinct, continued by postrostral carina and fading just anterior to postrostral tubercle. Extra-corneal teeth ( +Fig. 10b–d +) triangular, subacute distally. Pterygostomial angle ( +Fig. 10a, c +) bluntly or subacutely produced anteriorly. Cardiac notch ( +Fig. 10a +) deep. + + +Pleon ( +Fig. 10e +) glabrous; first to fifth pleura rounded distoventrally; sixth pleonite with subtriangular articulated plate. Telson ( +Fig. 10f +) moderately broad, gently tapering distally, about 2.1 times as long as proximal width; dorsal surface with two pairs of small spiniform setae situated at some distance from lateral margins, approximately at 0.50–0.55 (anterior) and 0.70–0.75 (posterior) of telson length; posterior margin slightly rounded, with two pairs of spiniform setae, mesial almost three times as long as lateral. + + + +FIGURE 10. + +Athanopsis dawa + + +sp. nov. + +, holotype, female (cl 4.4 mm) from Masirah Island, Oman (FLMNH UF 71424), a, carapace, lateral; b, frontal region, dorsal; c, same, lateral; d, rostrum, orbital teeth, postrostral tubercle and eye, lateral; e, posterior portion of fifth pleonite and sixth pleonite, lateral; f, telson, dorsal; g, tooth of ventromesial carina of first article of antennular peduncle, lateral; h, third maxilliped, lateral; i, same, tip of ultimate article, lateral; j, uropod, dorsal. + + + + +FIGURE 11. + +Athanopsis dawa + + +sp. nov. + +, holotype, female (cl 4.4 mm) from Masirah Island, Oman (FLMNH UF 71424), right cheliped, lateral; b, same, mesial; c, same, carpus and chela, mesial; d, same, chela fingers closed, mesial; e, same, chela fingers open, mesial; f, second pereiopod, lateral; g, third pereiopod, lateral; h, same, distal portion of carpus, propodus and dactylus, mesial; i, distal portion of propodus and dactylus, lateral; j, fourth pereiopod, lateral; k, same, distal portion of carpus, propodus and dactylus, mesial; l, fifth pereiopod, lateral; m, same, distal portion of carpus, propodus and dactylus, mesial; n, same, distal portion of propodus and dactylus, lateral + + + + +FIGURE 12. + +Athanopsis dawa + + +sp. nov. + +, holotype, female (cl 4.4 mm) from Masirah Island, Oman (FLMNH UF 71424) [a, b] and species’ habitat [c]; a, shrimp in life, lateral (left side); b, same, dorsal; c, type locality, sandflat with some seagrass and coral rubble, near Dafiyat, Masirah Island, Oman. Photographs by the author [a, b] and Gustav Paulay [c]. + + + +Eyes ( +Fig. 10a, b, d +) largely exposed dorsally and laterally, with well pigmented but slightly reduced corneas; anteromesial margin of eyestalks rounded, unarmed. + + +Antennule ( +Fig. 10b, c, g +) stout; stylocerite with blunt tip, reaching mid-length of third article of peduncle; ventromesial carina with large, anteriorly directed, sharp tooth; second article about 0.8 times as long as wide; lateral flagellum with fused portion composed of four units, accessory ramus well developed, subdivided into at least six poorly individualised units, each carrying group of two or three aesthetascs. + + +Antenna ( +Fig. 10b, c +) with basicerite stout, its distolateral margin armed with large, sharp tooth; scaphocerite broad, short, reaching slightly beyond end of antennular peduncle; lateral margin straight; anterior margin of blade rounded, greatly exceeded by stout distolateral tooth; carpocerite very stout, slightly overreaching both antennular peduncle and scaphocerite; flagellum thickened. + + +Mouthparts not dissected, typical for genus in external observation. Third maxilliped ( +Fig. 10h, i +) relatively stout; coxa with somewhat produced, distally acute lateral plate above mastigobranch; antepenultimate article noticeably broadened, with strongly convex dorsal margin, about 3.2 times as long as maximal width; penultimate article subrectangular, about 1.7 times as long as wide; ultimate article much slenderer and almost three times as long as penultimate article, tapering distally, with tip armed with one long and two short spiniform setae; exopod well developed, not reaching penultimate article. + + +First pereiopods (= chelipeds) about equal in size, symmetrical in shape, carried folded ventrally when not in use ( +Figs. 11a–e +, +12a +); basis with rudimentary exopod; ischium stout, widening distally, with three spiniform setae on dorsal margin, ventral surface unarmed; merus not particularly swollen, about four times as long as wide, with deeply excavated ventral surface, slightly convex dorsal margin and somewhat concave ventrolateral margin, all surfaces smooth; carpus very short, cup-shaped, smooth; chela slightly longer than merus; palm feebly swollen, depressed ventrolaterally, about three times as long as high (wide) in mesial view of chela, smooth; fingers 0.7 times as long as palm, strongly curved laterally, noticeably deviating from axis of palm, slender, fitting tightly when closed except for small gape proximally; cutting edge of pollex with with broad hiatus proximally followed by low triangular tooth at about proximal third of pollex, this tooth being continued by straight edge to fingertip; cutting edge of dactylus with three subtriangular, blunt teeth opposed to hiatus on pollex, remaining edge smooth. + + +Second pereiopod ( +Fig. 11f +) relatively short and rather stout; ischium about 2.6 times as long as distal width, distally widening, somewhat depressed on ventromesial surface; merus about 1.6 times as long as ischium, stout, 3.5 times as long as wide; carpus with five subarticles, proximal as long as sum of four others; chela longer than distal-most carpal subarticle, simple, with fingers equal to palm. Third to fifth pereiopods relatively stout, similar in length. Third pereiopod ( + +Fig. +11g +–i + +) with ischium armed with two spiniform setae on ventrolateral surface and one spiniform seta on distodorsal margin; merus about 1.6 times as long as ischium, 3.5 times as long as maximal width, not particularly swollen, ventrolateral margin distally with small subacute tooth; carpus noticeably more slender than merus, about half-length of merus, with two spiniform setae on distoventral margin; propodus about 1.8 times as long as carpus, slenderer than carpus, with seven spiniform setae on ventral or ventromesial margin, and one pair of spiniform setae distally, flanking base of dactylus; dactylus simple, slender, strongly curved, about 0.4 length of propodus. Fourth pereiopod ( +Fig. 11j, k +) generally similar to third pereiopod, slenderer; ischium armed with two spiniform setae on ventrolateral surface and one spiniform seta on distodorsal margin; merus 3.3 times as long as maximal width, ventrolateral margin distally with small subacute tooth; carpus about half-length of merus, with two spiniform setae on distoventral margin; propodus with seven spiniform setae on ventral or ventromesial margin, and one pair of spiniform setae distally, flanking base of dactylus; dactylus similar to that of third pereiopod. Fifth pereiopod ( +Fig. 11l–n +) shortest and slenderest of walking legs; ischium unarmed; merus about twice as long as ischium, about 3.2 times as long as wide, ventrolateral margin distally with small subacute tooth; carpus 0.6 length of merus, with two spiniform setae on distoventral margin; propodus with six spiniform setae on ventral or ventromesial margin, one pair of spiniform setae distally, flanking base of dactylus, and three rows of microserrulate setae on distolateral surface; dactylus similar to that of third or fourth pereiopods. + + +Uropod ( +Fig. 10j +) with lateral lobe of protopod enlarged, produced distally, with larger, triangular lateral tooth and smaller, blunt mesial tooth; exopod with stout distolateral tooth and long adjacent spiniform seta, latter almost reaching level of distal margin; diaeresis straight for most part, with low lateral lobe; endopod ovoid, as long as exopod. + +Gill-exopod formula as given for genus. + +Colour in life +. Background translucent whitish, with pale yellow tinge in females; carapace with bright red patch on rostro-orbital area, one narrow red band fringing each anterolateral margin, one much broader, more irregular transverse band extending from each branchial margin to cardiac region, not joining dorsally, and one very broad, white, transverse band covering almost entire area adjacent to posterior margin from dorsal mid-line to just above posterior-most portion of branchiostegial margin; pleon with four bright red, moderately narrow, transverse bands, more precisely on first, second, fourth and fifth pleonites, third pleonite with conspicuous, white, transverse band, sixth pleonite with broader, ring-like, white band; remaining appendages hyaline whitish; eggs / ovaries yolky yellow ( +Fig. 12a, b +). + + + + +Etymology +. The new species name refers to dhow (Arabic داو, latinised: + +dāwa + +), a generic name for traditional sailing vessels commonly seen in the western Indian Ocean from the Red Sea to the Arabian-Persian Gulf and +Zanzibar +; used as a noun in apposition. + + + + + + +Type +locality + +. +Masirah Island +, +Oman + +. + + + + +Distribution +. Currently known only from Masirah Island in +Oman +. + + + + +Ecology +. Both +type +specimens were extracted from presumably echiuran burrows on a shallow sandflat with patches of seagrass and coral rubble ( +Fig. 12c +), at a depth less than +0.5 m +at low tide. + + + + +Remarks +. + +Athanopsis dawa + + +sp. nov. + +can be easily distinguished from all other species of + +Athanopsis + +by two features, both being novel for this genus. The rather conspicuous postrostral tubercle on the carapace is a unique and highly diagnostic feature of the new species, as are the almost equal and subsymmetrical chelipeds ( +Figs. 11a, b +, +12a +). All other species of + +Athanopsis + +lack such a tubercle and have very unequal and asymmetrical chelipeds. It must be noted that both +type +specimens of + +A. dawa + + +sp. nov. + +are females and that the male condition of the chelipeds is currently unknown. Nevertheless, in other species of + +Athanopsis + +, the relative development of the right and left cheliped is similar between males and females (e.g., +Anker 2012 +: fig. 6; + +Marin +et al. +2014 + +: fig. 6). + + +The lack of armature (in the form of spiniform setae) on the merus of the third and fourth pereiopods places + +A. dawa + + +sp. nov. + +closest to + +A. brevirostris + +, + +A. saurus + +(see above), + +A. platyrhynchus +Coutière, 1897 + +, + +A. tarahomii +Marin, Sheibani & Sari, 2014 + +and + +A. gotoi +Anker, 2012 + +. However, all of them present several significant differences, in addition to lacking the post-rostral tubercle on the carapace and having very unequal and asymmetrical chelipeds. + +Athanopsis dawa + + +sp. nov. + +can be separated from + +A. brevirostris + +by the relatively longer second article of the antennular peduncle, which is as long as wide ( +vs. +much wider than long in + +A. brevirostris + +); from + +A. saurus + +by the lateral margins of the rostrum shallowly concave throughout their length ( +vs +. distinctly convex proximally in + +A. saurus + +); from both + +A. brevirostris + +and + +A. saurus + +by the absence of dense setal cover on parts of the major chela ( +vs +. with fields of setae on the fingers and distal portion of the palm in + +A. brevirostris + +and + +A. saurus + +); from + +A. platyrhynchus + +, + +A. tarahomii + +and + +A. gotoi + +by the much longer stylocerite, by far exceeding the distal margin of the second article of the antennular peduncle ( +vs +. reaching only to the mid-length of the second article in + +A. platyrhynchus + +and + +A. tarahomii + +, or falling short of this article’s distal margin in + +A. gotoi + +); from + +A. tarahomii + +by the noticeably slenderer third and fourth pereiopods (which are very stout in + +A. tarahomii + +), the third maxilliped with a proportionally longer and more rectangular-shaped penultimate article ( +vs +. with a very short, almost rounded, dorsally convex penultimate article in + +A. tarahomii + +), and the rostrum pointing forwards ( +vs +. descending in + +A. tarahomii + +); and from + +A. gotoi + +by the dorsally partly exposed eyes (which are dorsally concealed by the orbital hoods in + +A. gotoi + +) and the absence of tubercles on the ventral surface of the chelae (which are present in the major chela of + +A. gotoi + +) (cf. +Coutière 1899 +; +Banner & Banner 1981 +; Anker 2011, 2012; + +Marin +et al +. 2014 + +). The colour patterns are known for + +A. brevirostris + +( +Anker 2012 +; see also +Fig. 8 +), + +A. saurus + +(Anker 2011, 2012; see also +Fig. 9 +), + +A. tarahomii + +( +Fig. 14 +; not + +Marin +et al +. 2014 + +: fig. 7, see below), and + +A. gotoi +( +Anker 2012 +) + +and are different from that of + +A. dawa + + +sp. nov. + +( +Fig. 12a, b +). The colour pattern of + +A. platyrhynchus + +remains known only from +Coutière’s (1897 +, +1899 +) brief description (see +Anker 2012 +for translation). Generally, the taxonomic identity of + +A. platyrhynchus + +, the +type +species of the genus known with certainty only from +Djibouti +, remains problematic, as pointed out by +Anker (2012) +. + + +The remaining species of + +Athanopsis + +, i.e., + +A. dentipes +Miya, 1980 + +, + +A. australis +Banner & Banner 1982 + +and + +A. rubricinctuta +Berggren, 1991 + +(see below), are characterised by the presence of spiniform setae on the meri of the third, fourth and fifth pereiopods and present several other morphological differences with the new species (cf. +Miya 1980 +; +Banner & Banner 1982 +; +Berggren 1991 +; +Anker & Ahyong 2007 +). In addition, the colour patterns of + +A. dentipes + +and + +A. australis + +(cf. +Miya 1980 +; +Anker 2012 +) are very different from that of + +A. dawa + + +sp. nov. + +( +Fig. 12a, b +). On the other hand, the colour patterns of + +A. dawa + + +sp. nov. + +( +Fig. 12a, b +) and + +A. rubricinctuta + +( +Fig 13 +; see also +Anker 2012 +: fig. 7F, G) are very similar, to the extent that the two species may be easily confused in the field. However, at a closer inspection, + +A. dawa + + +sp. nov. + +can be distinguished from + +A. rubricinctuta + +by the white transverse band on the carapace descending from the dorsal area almost to the branchiostegial margin ( +vs +. being limited to the dorsal area in + +A. rubricinctuta + +) and the presence of an additional white transverse band on the third pleonite (which is missing in + +A. rubricinctuta + +). + + + + \ No newline at end of file diff --git a/data/38/6A/BE/386ABE42FFA9FFB3FF06ABF52C1EFC00.xml b/data/38/6A/BE/386ABE42FFA9FFB3FF06ABF52C1EFC00.xml new file mode 100644 index 00000000000..215178f80a5 --- /dev/null +++ b/data/38/6A/BE/386ABE42FFA9FFB3FF06ABF52C1EFC00.xml @@ -0,0 +1,340 @@ + + + +Alpheid shrimps of the genera Athanas Leach, 1814, Athanopsis Coutière, 1897 and Pseudathanas Bruce, 1983 of the coasts of the Arabian Peninsula (Malacostraca: Decapoda: Caridea) + + + +Author + +Anker, Arthur +Universidade Federal de Pelotas (UFPEL), Departamento de Ecologia, Zoologia e Genética, Instituto de Biologia, Campus Universitário Capão do Leão, RS, 96010 - 610, Brazil & Red Sea Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia + +text + + +Zootaxa + + +2023 + +2023-12-11 + + +5383 + + +2 + + +179 +215 + + + + +https://www.mapress.com/zt/article/download/zootaxa.5383.2.5/52448 + +journal article +10.11646/zootaxa.5383.2.5 +1175-5326 +10350767 +7E434B40-6346-4E6D-BC55-38EBAE24BD52 + + + + + + + +Athanopsis tarahomii +Marin, Sheibani & Sari, 2014 + + + + + + + +( +Fig. 14 +) + + + + + + + +Athanopsis tarahomii + +Marin +et al. +2014: 404 + + + +(part., not “Coloration” on p. 409), figs. 4–6 (not fig. 7). + + + + +Not + +Athanopsis tarahomii + +— + + +Marin +et al. +2014: 408 + + +, fig. 7, 409 (“Coloration”) [= + +Amphibetaeus jousseaumei +( +Coutière, 1896 +) + +, see below]. + + + + + +Material examined +. + +1 male +(cl +4.6 mm +), 1 ovig. female (cl +4.7 mm +), +FLMNH +UF 71425 +, +Saudi Arabia +, +Thuwal +, near +KAUST +King Abdullah Monument +, +22°20’26.2”N +/ +39°05’15.1”E +, shallow subtidal sandflat with seagrass and rubble patches, depth + +0.5–1.5 m + +, suction pump, in echiuran burrow, leg. +A. Anker +, + +20.01.2023 + +[fcn AA-22-493] + +. + + + + +Description +. See + +Marin +et al. +(2014) + +for original description and illustrations; colour photographs of the +Red Sea +specimens are provided in +Fig. 14 +. + + +Colour in life +. Background translucent whitish; carapace with small red patch between eyes, numerous white, star-shaped chromatophores covering most of dorsal surface, and broad, red patch on each flank, at about middle of carapace; most of pleon densely covered with white chromatophores, ventral pleura of third pleonite and most of fourth pleonite deep red; chelipeds and remaining appendages hyaline whitish; eggs yolky yellow ( +Fig. 14 +). See also remarks below. + + + + +FIGURE 13. + +Athanopsis rubricinctuta +Berggren, 1991 + +, male (cl 5.4 mm) from Masirah Island, Oman (FLMNH UF 71437) [a, b]; male (cl 5.8 mm) from the same locality (FLMNH UF 71443) [c]; a, shrimp in life, lateral (right side); b, same, dorsal; c, shrimp in life (different individual), lateral (left side). Photographs by the author. + + + + +FIGURE 14. + +Athanopsis tarahomii +Marin, Sheibani & Sari, 2014 + +, male (cl 4.6 mm) [a, b] from Thuwal, Saudi Arabia (FLMNH UF 71425); ovigerous female (cl 4.7 mm) from the same locality (same burrow) (FLMNH UF 71425) [c, d]; a, shrimp in life (male), lateral (left side); b, same, dorsal; c, shrimp in life (female), lateral (right side); d, same, dorsal. Photographs by the author. + + + + + +Type +locality + +. +Qeshm Island +, +Iran +. + + + + +Distribution +. Currently known only from the +type +locality in +Iran +( + +Marin +et al +. 2014 + +) and the Red Sea coast of +Saudi Arabia +(present study). + + + + +Ecology +. The two Saudi Arabian specimens were extracted from the burrow of a large echiuran (probably + +Ochetostoma +sp. + +) on a shallow sandflat with large patches of seagrass and some fragmented rubble, at a depth of about + +1 m +. + +The Iranian +type +specimens were also found in association with echiurans, in a “cobble/rocky area under large boulder” ( + +Marin +et al +. 2014 + +). + + + + +Remarks +. + +Athanopsis tarahomii + +was hitherto known only from +two type +specimens from +Qeshm Island +, +Iran +, in the Strait of +Hormuz +. The present Saudi Arabian material of + +A. tarahomii + +significantly extends its previously known range from the Arabian-Persian Gulf to the central Red Sea. The two Red Sea specimens agree well with the +type +material, including the very characteristic descendant and distally notched rostrum, although not as pronounced as in the +type +specimens ( + +Marin +et al +. 2014 + +: fig. 4d, e). + + +The colour pattern of + +A. tarahomii + +is herein illustrated for the first time ( +Fig. 14 +) and is diagnostic for this species, despite possessing some similarities with the colour patterns of + +A. brevirostris + +and + +A. saurus + +(cf. +Figs. 8 +, +9 +). The description of the colour pattern of + +A. tarahomii + +and the accompanying photograph in + +Marin +et al. +(2014 + +: fig. 7) are erroneous and actually refer to + +Amphibetaeus jousseaumei +( +Coutière, 1896 +) + +, which was reported in the same study. The present author is in the possession of a colour photograph showing two individuals (presumably type specimens) of the real + +A. tarahomii + +from +Qeshm Island +[sent by R. Sheibani, the second author in + +Marin +et al +. (2014) + +well before the publication of their study), which confirms that the colour patterns of the Iranian and Saudi Arabian specimens are almost identical. Another error in + +Marin +et al. +(2014) + +is the invalid designation of a +neotype +for + +A. jousseaumei + +(SMF-43232, deposited in the Senckenberg Naturmuseum, Frankfurt) as a +lectotype +exists for this species (see +Anker & Jeng 2006 +). + + + + \ No newline at end of file diff --git a/data/38/6A/BE/386ABE42FFA9FFB6FF06AEDA2D41FAD1.xml b/data/38/6A/BE/386ABE42FFA9FFB6FF06AEDA2D41FAD1.xml new file mode 100644 index 00000000000..e22c3945331 --- /dev/null +++ b/data/38/6A/BE/386ABE42FFA9FFB6FF06AEDA2D41FAD1.xml @@ -0,0 +1,246 @@ + + + +Alpheid shrimps of the genera Athanas Leach, 1814, Athanopsis Coutière, 1897 and Pseudathanas Bruce, 1983 of the coasts of the Arabian Peninsula (Malacostraca: Decapoda: Caridea) + + + +Author + +Anker, Arthur +Universidade Federal de Pelotas (UFPEL), Departamento de Ecologia, Zoologia e Genética, Instituto de Biologia, Campus Universitário Capão do Leão, RS, 96010 - 610, Brazil & Red Sea Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia + +text + + +Zootaxa + + +2023 + +2023-12-11 + + +5383 + + +2 + + +179 +215 + + + + +https://www.mapress.com/zt/article/download/zootaxa.5383.2.5/52448 + +journal article +10.11646/zootaxa.5383.2.5 +1175-5326 +10350767 +7E434B40-6346-4E6D-BC55-38EBAE24BD52 + + + + + + + +Athanopsis rubricinctuta +Berggren, 1991 + + + + + + + +( +Fig. 13 +) + + + + + + + +Athanopsis rubricinctuta +Berggren 1991: 166 + + +, figs. 1–6. + + + + + +Material examined +. + +1 male +(cl +5.5 mm +), +FLMNH +UF 71437 +, +Oman +, +Masirah Island +, channel side, +Dafiyat +, +20°35’15.1”N +/ +58°49’36.9”E +, intertidal and shallow subtidal sandflat with patches of coral rubble, rocks and seagrass, depth at low tide less than + +0.5 m + +, suction pump, in echiuran burrow, leg. +A. Anker +, + +07.11.2022 + +[fcn BOMAN-13029, specimen infested with a pair of hemiarthrine isopods] + +; + +1 male +(cl +5.4 mm +), +FLMNH +UF 71437 +, same collection data as for previous specimen [fcn BOMAN-13015] + +; + +1 male +(cl +5.8 mm +), +FLMNH +UF 71443 +, same collection data as for previous specimen [fcn BOMAN-13016]; 1 ovig. female (cl 5.0 mm), +FLMNH +UF 71440 +, same collection locality as for previous specimens, in echiuran burrow with numerous + +Rissoina +sp. + +, leg. +A. Anker +, + +19.11.2022 + +[fcn BOMAN-14802] + +. + + + + +Description +. See +Berggren (1991) +for original description and illustrations; colour photographs of the Omani specimens are provided in +Fig. 13 +. + + +Colour in life +. Background translucent whitish; carapace with bright red patch on rostro-orbital area, one narrow red band fringing each anterolateral margin, one much broader, more irregular transverse band extending from each branchial margin to cardiac region, however, not joining dorsally, and white transverse band on dorsal surface, near posterior margin; pleon with four bright red, moderately narrow, transverse bands, more precisely on first, second, fourth and fifth pleonites, sixth pleonite with white dorsal patch; remaining appendages hyaline whitish ( +Fig. 13 +); see also +Berggren (1991 +: fig. 6) and +Anker (2012 +: fig. 7F, G). + + + + + + +Type +locality + +. +Inhaca Island +, +Mozambique + +. + + + + +Distribution +. Currently known only from the +type +locality in +Mozambique +( +Berggren 1991 +) and Masirah Island, +Oman +(present study). + + + + +Ecology +. All specimens were extracted from echiuran (probably + +Ochetostoma +sp. + +) burrows on a shallow sandflat with patches of seagrass and rubble, at a depth of +0.5 m +or less at low tide. The +type +specimens were found in the intertidal, in association with “echiuroids of the family +Thalassematidae +” ( +Berggren 1991 +). + + + + +Remarks +. + +Athanopsis rubricinctua + +was hitherto known only from the type series from Inhaca Island, +Mozambique +. The finding of several specimens of + +A. rubricinctuta + +in +Oman +considerably extends the previously known range of the species in the western Indian Ocean. The Omani material agrees very well with +Berggren’s (1991) +type material, including the dorsally partly exposed eyes due to the reduction of orbital teeth, with only minor variation observed, for instance, in the armature of the merus of the third, fourth and fifth pereiopods (with one or two spiniform setae in the Omani specimens +vs +. with one spiniform seta in the +holotype +). The colour pattern of the Omani specimens ( +Fig. 11 +) is very similar to that of the Mozambiquan specimens ( +Berggren 1991 +: fig. 6; +Anker 2012 +: fig. 7F, G) and is highly diagnostic for the species. + + + + \ No newline at end of file diff --git a/data/38/6A/BE/386ABE42FFACFFB1FF06ADBB2C8FFD68.xml b/data/38/6A/BE/386ABE42FFACFFB1FF06ADBB2C8FFD68.xml new file mode 100644 index 00000000000..043bb6eb4bf --- /dev/null +++ b/data/38/6A/BE/386ABE42FFACFFB1FF06ADBB2C8FFD68.xml @@ -0,0 +1,629 @@ + + + +Alpheid shrimps of the genera Athanas Leach, 1814, Athanopsis Coutière, 1897 and Pseudathanas Bruce, 1983 of the coasts of the Arabian Peninsula (Malacostraca: Decapoda: Caridea) + + + +Author + +Anker, Arthur +Universidade Federal de Pelotas (UFPEL), Departamento de Ecologia, Zoologia e Genética, Instituto de Biologia, Campus Universitário Capão do Leão, RS, 96010 - 610, Brazil & Red Sea Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia + +text + + +Zootaxa + + +2023 + +2023-12-11 + + +5383 + + +2 + + +179 +215 + + + + +https://www.mapress.com/zt/article/download/zootaxa.5383.2.5/52448 + +journal article +10.11646/zootaxa.5383.2.5 +1175-5326 +10350767 +7E434B40-6346-4E6D-BC55-38EBAE24BD52 + + + + + + +Genus + +Pseudathanas +Bruce, 1983 + + + + + + + + + + +Alberta +Kazmi & Kazmi 2010: 233 + + +. + + + + + +Emended diagnosis +. Body not compressed, not particularly slender. Carapace smooth, unarmed dorsally and laterally. Rostrum broadly triangular, unarmed dorsally and ventrally. Orbital teeth absent or reduced. Pterygostomial angle rounded, not protruding; posteroventral margin of branchiostegite fringed with long plumose setae; cardiac notch well developed. All pleonites with distoventrally rounded pleura; sixth pleuron with articulated plate. Telson moderately broad, with two pairs of stout spiniform setae on dorsal surface; posterior margin rounded, with two pairs of spiniform setae; anal tubercles absent. Eyes well developed, partly visible or concealed in dorsal view; cornea large, well pigmented. Antennular peduncle stout, relatively short; stylocerite well developed, distally acute, overreaching mid-length of second article of peduncle; ventromesial carina armed with tooth; second article not particularly elongate; lateral flagellum with short fused portion and well-developed accessory ramus with aesthetascs. Antenna with basicerite stout, unarmed or armed with small sharp tooth; scaphocerite with well-developed blade and small distolateral tooth. Mandible with two-articulated palp; molar and incisor processes well developed. Third maxilliped with well-developed exopod; coxa with acutely produced lateral plate; ultimate article tapering into corneous tip, unarmed. First pereiopods (= chelipeds) enlarged in both sexes, unequal or subequal in size, asymmetrical or subsymmetrical in shape, carried flexed beneath body when not in use; ischium robust, with dorsal and ventral margins rugose and armed with short spiniform setae; merus with ventrolateral margin rugose and armed with prominent tooth near its mid-length, ventral surface deeply excavated; carpus vase- or cup-shaped, without setal rows on mesial surface; chelae more or less swollen; palm with tubercles and row of setae on ventral surface; fingers of major chela armed with large teeth, without snapping mechanism. Second pereiopod with ischium unarmed; carpus with four or five subarticles; chela simple, without modifications. Third and fourth pereiopods moderately slender; ischium armed with one or two spiniform seta(e); merus unarmed; carpus with one spiniform seta on distoventral margin; propodus with several spiniform setae; dactylus simple, conical. Fifth pereiopod with ischium armed with one spiniform seta; merus unarmed; carpus with one spiniform seta on distoventral margin; propodus with at least two spiniform setae and short cleaning brush; dactylus simple. Second male pleopod with appendix masculina subequal in length to appendix interna; second female pleopod with appendix interna only. Uropodal exopod with diaeresis armed with row of stout spiniform setae. Gill-exopod formula provided in +Table 3 +. + + + +TABLE 3 +. Gill-exopod formula of + +Pseudathanas +Bruce, 1983 + +. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Gills/exopodsMaxillipedsPereiopods
Mxp1Mxp2Mxp3P1P2P3P4P5
Pleurobranchs---11111
Arthrobranchs--------
Podobranchs--------
Epipods+++1-----
Mastigobranchs2--++++--
Setobranchs---++++-
Exopods+++-3----
+
+ +1, 2 + + +same remarks as for Table 1. +3 +needs confirmation. + + +Species included +. +Type +species + +P. darwiniensis +Bruce, 1983 + +; + +P. banneri +( +Kazmi & Kazmi, 2010 +) + + +comb. nov. + + +
+ + +Remarks +. The alpheid genus + +Pseudathanas + +was originally established to accommodate only the +type +species + +Pseudathanas darwiniensis +Bruce, 1983 + +, a small, peculiar, intertidal shrimp found in silted rock pools near Darwin, +Northern Territory +, +Australia +( +Bruce 1983 +). + +Pseudathanas + +was separated from the closely related genus + +Athanas + +by the much shorter rostrum, the greatly reduced orbital teeth, the proximally thickened antennal flagella, the unequal and asymmetrical chelipeds, and the presence of stout spiniform setae on the transverse suture (diaeresis) of the uropodal exopod ( +Bruce 1983 +), this latter feature being unique within the +Alpheidae +and therefore most diagnostic of the genus. No other specimens of + +Pseudathanas + +have been reported since +Bruce’s (1983) +description of + +P. darwiniensis + +and the genus remained monotypic for almost 40 years. + + +In the poorly known, not peer-reviewed publication (book) on the caridean shrimps of +Pakistan +, +Kazmi & Kazmi (2010) +established the alpheid genus + +Alberta +Kazmi & Kazmi, 2010 + +for + +Alberta banneri +Kazmi & Kazmi, 2010 + +, based on a single ovigerous female from Bulleji, near Karachi. All material listed in this study, including the +holotype +of + +A. banneri + +, was supposedly deposited in the Marine Reference Collection and Resource Centre, University of Karachi, +Pakistan +. The generic diagnosis of + +Alberta + +, as well as the description of its type species + +A. banneri + +, are very poor compared to modern standards in caridean taxonomy. Nevertheless, the semi-diagrammatic illustrations of + +A. banneri + +provided by +Kazmi & Kazmi (2010) +are sufficient to suggest that this taxon belongs to the genus + +Pseudathanas + +. Most importantly, the diaeresis of the uropodal exopod of + +A. banneri + +is adorned with the same row of strong spiniform setae as in + +P. darwiniensis + +(cf. +Bruce 1983 +: fig. 2F, 5C; +Kazmi & Kazmi 2010 +: fig. 108B). The collection of +three specimens +(one subsequently lost) of a species with all characteristics of + +A. banneri + +in northern +Oman +(see below) eliminated any lingering doubts about its identity. Therefore, + +Alberta + +is herein placed in the synonymy of + +Pseudathanas + +and the Omani material is reported as + +Pseudathanas banneri +( +Kazmi & Kazmi, 2010 +) + + +comb. nov. + +The generic diagnosis of + +Pseudathanas + +provided above was emended to accommodate several features of + +P. banneri + +that are novel for the genus, especially the dorsally covered eyes, the subequal and subsymmetrical chelipeds, and the second pereiopod carpus with four subarticles (carpal subdivisions). + + +As suggested by +Bruce (1983) +, + +Pseudathanas + +is closely related to + +Athanas + +, from which it differs essentially by the armature of the diaeresis.All other morphological characters listed by +Bruce (1983) +to distinguish + +Pseudathanas + +from + +Athanas + +are invalid as they are present in some more recently described species of the latter genus (see also above). These characters are the marked reduction of the rostrum (also observed in + +A. iranicus + +, + +A. daviei + +, + +A. manticolus + +, + +A. claereboudti + + +sp. nov. + +); the absence of supra-, extra-, or infra-corneal teeth (absent or greatly reduced in + +A. iranicus + +, + +A. daviei + +, + +A. manticolus + +and + +A. claereboudti + + +sp. nov. + +); the well-developed, dissimilar chelipeds, apparently in both males and females (female minor cheliped unknown in + +P. darwinensis + +) (variable in + +Athanas + +, with similar condition found, for instance, in + +A. shawnsmithi + +); and the proximally thickened antennal flagellum (also observed in + +A. iranicus + +, + +A. shawnsmithi + +, + +A. manticolus + +and + +A. claereboudti + + +sp. nov. + +). + +Pseudathanas + +also shares many features with + +Athanopsis +Coutière, 1897 + +and + +Leptathanas +De Grave & Anker, 2008 + +, differing from both of these genera by the unique armature of the uropodal diaeresis; from + +Athanopsis + +by the distally pointed rostrum ( +vs +. rounded in + +Athanopsis + +); and from + +Leptathanas + +by the relatively well developed rostrum (reduced in + +Leptathanas + +) and the much slenderer walking legs and antennular peduncles (very stout in + +Leptathanas + +) (cf. +Coutière 1897 +, +1899 +; +Anker & Ahyong 2007 +; +De Grave & Anker 2008 +; +Anker 2011b +, +2012 +; + +Marin +et al. +2014 + +, see also +Fig. 10 +). The long plumose setae on the posteroventral margin of the branchiostegite are present in + +Pseudathanas + +, but also in the not closely related + +Orygmalpheus +De Grave & Anker, 2000 + +and (with lesser development) in some other alpheid genera ( +De Grave & Anker 2000 +; + +Anker +et al. +2006a + +). + + + +Anker +et al. +(2006a) + +performed a cladistic analysis of morphological characters and recovered + +Pseudathanas + +and + +Athanas + +in sister position within a larger “athanoid” clade (clade AP), together with + +Athanas + +(paraphyletic), + +Arete +Stimpson, 1860 + +and + +Aretopsis +De Man, 1910 + +. In the molecular analysis of the + +Alpheidae, + +Chow +et al. +(2021) + + +also recovered an athanoid clade (clade S-V), which further included + +Acanthanas +Anker, Poddoubtchenko & Jeng, 2006 + +( + +Anker +et al. +2006b + +). + +Pseudathanas + +and + +Leptathanas + +were not included in their analysis because no suitable material of these genera was available at that time. Interestingly, + +Chow +et al. +(2021) + +showed + +Athanas + +and + +Arete + +to be non-monophyletic due to the positions of two species of + +Athanopsis + +and one species of + +Athanas + +, respectively. Surprisingly, and difficult to explain from the morphological point of view, + +Rugathanas +Anker & Jeng 2007 + +was excluded from clade S-V despite the presence of several synapomorphic features linking it to other athanoid genera ( +Anker & Jeng 2007 +). Based on its overall morphology, + +Pseudathanas + +appears to be closest to + +Athanopsis + +and is most likely nested within the + +Athanas + ++ + +Athanopsis + +lineage of + +Chow +et al. +(2021) + +, whilst the phylogenetic position of the highly derived + +Leptathanas + +remains more enigmatic. The entire athanoid clade will definitively need more phylogenetic efforts devoted to it, in view of interesting evolutionary convergences due to symbiotic lifestyles (both infaunal and epibiotic, see +Anker & Jeng 2007 +). + + +
+
\ No newline at end of file diff --git a/data/38/6A/BE/386ABE42FFAEFF8FFF06AD532B03F944.xml b/data/38/6A/BE/386ABE42FFAEFF8FFF06AD532B03F944.xml new file mode 100644 index 00000000000..d5a2045d22b --- /dev/null +++ b/data/38/6A/BE/386ABE42FFAEFF8FFF06AD532B03F944.xml @@ -0,0 +1,358 @@ + + + +Alpheid shrimps of the genera Athanas Leach, 1814, Athanopsis Coutière, 1897 and Pseudathanas Bruce, 1983 of the coasts of the Arabian Peninsula (Malacostraca: Decapoda: Caridea) + + + +Author + +Anker, Arthur +Universidade Federal de Pelotas (UFPEL), Departamento de Ecologia, Zoologia e Genética, Instituto de Biologia, Campus Universitário Capão do Leão, RS, 96010 - 610, Brazil & Red Sea Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia + +text + + +Zootaxa + + +2023 + +2023-12-11 + + +5383 + + +2 + + +179 +215 + + + + +https://www.mapress.com/zt/article/download/zootaxa.5383.2.5/52448 + +journal article +10.11646/zootaxa.5383.2.5 +1175-5326 +10350767 +7E434B40-6346-4E6D-BC55-38EBAE24BD52 + + + + + + + +Pseudathanas banneri +( +Kazmi & Kazmi, 2010 +) + + + + + + + +( +Figs. 15 +, +16 +) + + + + + + + +Alberta banneri +Kazmi & Kazmi 2010: 234 + + +, figs. 108, 109. + + + + + +Material examined +. + +1 male +(cl +6.7 mm +), +FLMNH +UF 68864 +, +Oman +, Muscat, +Qurum Beach +, +23°37’31.7”N +/ +58°28’45.8”E +, intertidal sandflat, depth at low tide less than + +0.2 m + +, suction pump, in burrow, leg. +A. Anker +, + +30.01.2022 + +[fcn BOMAN-10262] + +; + +1 male +(cl +5.5 mm +), +FLMNH +UF 68865 +, same collection data as for previous specimen [fcn BOMAN-10263] + +; + +1 female +(cl +6.45 mm +), same collection data as for previous specimen, same burrow [fcn BOMAN-10264, specimen not deposited, see below] + +. + + + + +FIGURE 15. + +Pseudathanas banneri +( +Kazmi & Kazmi, 2010 +) + + +comb. nov. + +, male (cl 6.7 mm) from Muscat, Oman (FLMNH UF 68864); a, right cheliped (drawn +in situ +), lateral; b, same, carpus and chela, mesial; c, left cheliped, distal portion of ischium, merus and carpus (drawn +in situ +), lateral. + + + + +FIGURE 16. + +Pseudathanas banneri +( +Kazmi & Kazmi, 2010 +) + + +comb. nov. + +, male (cl 6.7 mm) from Muscat, Oman (FLMNH UF 68864) [a, b]; female (cl 6.45 mm) from the same locality (not deposited, see text) [c–e]; a, shrimp in life (male), lateral (left side); b, same, dorsal; c, shrimp in life (female), frontal region, dorsal; d, e, left cheliped, lateral (d) and mesial (e). Photographs by the author. + + + + +Description +. See +Kazmi & Kazmi (2010) +for description and illustrations (as + +Alberta banneri + +); complementary figures of the chelipeds are provided in +Fig. 15 +(see also +Fig. 16d, e +); colour pattern of the species is described and illustrated for the first time (see below and +Fig. 16 +). + + +Colour pattern +. Body translucent with yellow tinge; carapace and pleon covered by bright red chromatophores, many of them resembling dendritic cells or chromosomes, pale yellowish chromatophores, and sometimes also with larger opaque blotches of white or pale yellowish chromatophores dorsolaterally (on carapace) or dorsally (on pleon); telson with few red chromatophores proximally and large blotches of white or pale yellowish chromatophores; antennular and antennal peduncles and bases of flagella with similar red and pale yellow chromatophores, distal part of flagella translucent whitish; chelipeds with yellowish and red chromatophores on dorsolateral surface of ischium and merus, carpus and chela hyaline white; second to fifth pereiopods and pleopods translucent whitish; uropodal endopod evenly speckled with yellow and large red chromatophores; uropodal exopod with large colourless “window”, with red and yellow chromatophores along lateral margin and in distal third, posterior to diaeresis ( +Fig. 16 +). +Kazmi & Kazmi (2010) +noted the colour of + +P. banneri + +(as + +A. banneri + +) as “off white (when fresh)”, probably describing a +post-mortem +specimen. + + + + +Distribution +. North-Western Indian Ocean: presently known only from two localities in the Arabian Sea: Karachi, +Pakistan +, and +Muscat +, +Oman +. + + + + +Ecology +. The three Omani specimens of + +P. banneri + +were extracted from burrows of an unknown fossorial animal on a relatively exposed, intertidal sandflat, in front of a small, degraded mangrove area. The substrate was composed of fine sand, patchily mixed with coarser sand, shells, shell fragments and small rocks and coral debris. All burrows, in which + +P. banneri + +was found, were located in a +5–10 m +wide runoff with brackish water streaming from the mangrove to the sea at low tide. The burrowing macrofauna included the mantis shrimp + +Bigelowina phalangium +( +Fabricius, 1798 +) + +and the ghost shrimp + +Neocallichirus +cf. +calmani +(Nobili, 1904) + +[identification requires confirmation], which are both known to host symbiotic alpheid shrimps ( +Ďuriš & Anker 2014 +; +Anker & Ashrafi 2019 +). The habitat and collection data for the +holotype +are unknown. + + + + +Remarks +. The Omani material of + +Pseudathanas banneri + +originally contained +three specimens +, +two males +(fcn BOMAN-10262, BOMAN-10263) and +one female +(fcn BOMAN-10264), from the same locality, only a few kilometres away from the historical centre of +Muscat +. Unfortunately, the only female, which was selected for dissection and line drawings, was lost during transportation, along with some other important decapod material (see Anker & Benzoni 2023). For this reason, the decision was made to leave the remaining +two male +specimens (FLMNH UF 68864, 68865) of this very rare genus and species as intact as possible. The chelipeds of one of the +two males +were drawn +in situ +( +Fig. 15 +), whereas the detached left female cheliped (subsequently lost together with the body of the specimen) is illustrated by colour photographs ( +Fig. 16d, e +). + + + +Pseudathanas banneri + +can be easily separated from + +P. darwiniensis + +by (1) the dorsally completely covered eyes ( +vs +. partly exposed in + +P. darwiniensis + +); (2) the stylocerite reaching slightly beyond half-length of the second article of the antennular peduncle ( +vs +. reaching to the end of this article in + +P. darwiniensis + +); (3) the subsymmetrical and subequal chelipeds ( +vs +. asymmetrical and unequal chelipeds in + +P. darwiniensis + +); (4) the ventrolateral margin of the cheliped merus crenulated and bearing a more prominent, distally more pointed tooth ( +vs +. margin smoother and with a broader and blunter tooth in + +P. darwiniensis + +); and (5) the second pereiopod carpus with four subarticles ( +vs +. five subarticles in + +P. darwiniensis + +) ( +Kazmi & Kazmi 2010 +: fig. 108; +Bruce 1983 +: figs. 2, 4). The colour patterns of the two species appear to be similar, at least judging from the brief description of the colour pattern of + +P. darwiniensis + +provided by +Bruce (1983) +. + + +Despite the fact that no symbiotic association was noted for the Australian species, + +P. darwiniensis + +, by +Bruce (1983) +, or for the +holotype +of + +P. banneri + +by +Kazmi & Kazmi (2010) +, both currently known species of + +Pseudathanas + +appear to be infaunal, commensal shrimps.This hypothesis is supported by the general morphology of + +P. darwiniensis + +and + +P. banneri + +, as well as by the collection method (suction or “yabby” pump) of the Omani specimens. + + + + \ No newline at end of file diff --git a/data/38/6A/BE/386ABE42FFB1FFACFF06AB872EC2FE08.xml b/data/38/6A/BE/386ABE42FFB1FFACFF06AB872EC2FE08.xml new file mode 100644 index 00000000000..cdf521286c5 --- /dev/null +++ b/data/38/6A/BE/386ABE42FFB1FFACFF06AB872EC2FE08.xml @@ -0,0 +1,325 @@ + + + +Alpheid shrimps of the genera Athanas Leach, 1814, Athanopsis Coutière, 1897 and Pseudathanas Bruce, 1983 of the coasts of the Arabian Peninsula (Malacostraca: Decapoda: Caridea) + + + +Author + +Anker, Arthur +Universidade Federal de Pelotas (UFPEL), Departamento de Ecologia, Zoologia e Genética, Instituto de Biologia, Campus Universitário Capão do Leão, RS, 96010 - 610, Brazil & Red Sea Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia + +text + + +Zootaxa + + +2023 + +2023-12-11 + + +5383 + + +2 + + +179 +215 + + + + +https://www.mapress.com/zt/article/download/zootaxa.5383.2.5/52448 + +journal article +10.11646/zootaxa.5383.2.5 +1175-5326 +10350767 +7E434B40-6346-4E6D-BC55-38EBAE24BD52 + + + + + + +Genus + +Athanas +Leach, 1814 + + + + + + + + + + +Athanas +Leach 1814: 401 + + +. + + + + + +Emended diagnosis +(simplified and updated from +Anker & Jeng 2007 +). Body not compressed, slender to moderately stout. Carapace smooth, glabrous or moderately setose, typically unarmed dorsally, sometimes with small postrostral tubercle. Rostrum typically elongate, sometimes lanceolate in dorsal view, rarely short, subtriangular; dorsal margin unarmed or with minute teeth; ventral margin unarmed. Orbital teeth usually present as one pair of extra-corneal tooth, often well developed and sometimes protruding beyond anterior margin of eye, and one pair of infra-corneal teeth; occasionally infra-corneal teeth reduced or absent; extra-corneal teeth occasionally reduced to small bumps; supra-corneal teeth absent (often) or present (rarely). Pterygostomial angle rounded or angular, sometimes produced as sharp tooth; branchiostegite with scarce setae; cardiac notch well developed. First to fourth pleonites with distoventrally rounded or bluntly angular pleura; fifth pleonite with pleuron angular or subacute distoventrally; sixth pleuron with articulated plate. Telson moderately slender to broad, tapering distally, with two pairs of stout spiniform setae on dorsal surface; posterior margin rounded or straight, with two pairs of spiniform setae; anal tubercles absent. Eyes well developed, at least partly visible in dorsal view; cornea large, well pigmented, sometimes slightly reduced. Antennular peduncle stout, relatively short; stylocerite well developed, distally acute or subacute, usually overreaching mid-length of second article, sometimes its distal margin; ventromesial carina armed with tooth; second article not or variously elongate; lateral flagellum with short fused portion and well-developed accessory ramus with aesthetascs.Antenna with basicerite moderately to very stout, armed with sharp tooth; scaphocerite with well-developed blade and variously developed distolateral tooth. Mandible with two-articulated palp; molar and incisor processes well developed. Third maxilliped with well-developed exopod; coxa with moderately produced lateral plate; ultimate article tapering into corneous tip, often with small spiniform seta(e). First pereiopods (= chelipeds) highly variable in development, often sexually dimorphic, typically greatly enlarged in males, sometimes in both sexes, subequal or very unequal in size, subsymmetrical or highly asymmetrical in shape, carried extended or flexed beneath body when not in use; basis typically with rudimentary exopod; ischium robust, with dorsal margin or both dorsal and ventral margins often armed with spiniform setae; merus with ventrolateral margin smooth or dentate, ventral surface flattened or deeply excavated; carpus variable, cylindrical, vase- or cup-shaped, without setal rows on mesial surface; chelae more or less enlarged and swollen, palm with or without tubercles and row of setae on ventral surface; fingers of chelae unarmed or armed with teeth, in males or in both sexes, without snapping mechanism. Second pereiopod with ischium unarmed; carpus typically with five, rarely four or six, subarticles; chela simple, without modifications. Third and fourth pereiopods varying from very slender to moderately stout; ischium usually armed with one spiniform seta, rarely with two spiniform setae or unarmed; merus unarmed; propodus with several spiniform setae or short stiff setae on ventral margin; dactylus more or less slender, simple or biunguiculate. Fifth pereiopod with ischium unarmed or armed with one spiniform seta; merus unarmed; propodus with or without spiniform setae and well-developed cleaning brush; dactylus simple or biunguiculate. Second male pleopod with appendix masculina equal in length or exceeding appendix interna, sometimes reaching beyond endopod; second female pleopod with appendix interna only. Uropodal exopod with unarmed, sinuous or straight diaeresis. Gill-exopod formula summarised in +Table 1 +. + + + +TABLE 1 +. Gill-exopod formula of + +Athanas +Leach, 1814 + +. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Gills/exopodsMaxillipedsPereiopods
Mxp1Mxp2Mxp3P1P2P3P4P5
Pleurobranchs---+++++
Arthrobranchs--------
Podobranchs--------
Epipods+++1-----
Mastigobranchs2--++++/-+/--
Setobranchs---++++/-+/-
Exopods++++3/-----
+
+ + +1 +lateral plate on coxa; +2 +strap-like epipods of +Chace (1988) +; +3 +if present, rudimentary. + + + +Species included +. +Type +species + +A. nitescens +( +Leach, 1814 +) + +; all species listed in +De Grave & Fransen (2011) ++ + +A. manticolus +Ďuriš & Anker, 2014 + +; + +A. mendax +Ahyong, 2015 + +; + +A. alpheusophilus +Marin, 2017 + +; + +A. philippei +Anker & Ďuriš 2022 + +; + +A. exilis +Komai & Henmi, 2023 + +; + +A. claereboudti + + +sp. nov. + +(described below). + +
+ + +Remarks +. + +Athanas + +and allied genera were reviewed and taxonomically redefined by +Anker & Jeng (2007) +. However, the rapidly increasing number of species, especially among the infaunal “commensals”, resulted in the much greater morphological heterogeneity of + +Athanas + +compared to the definition of the genus given by +Anker & Jeng (2007) +. In the herein emended generic diagnosis of + +Athanas + +, the author attempted to take into consideration all important novel features described in the genus (including the below-described new species) since its redefinition by +Anker & Jeng (2007) +. It is interesting to note that the infaunal lifestyle that evolved in some lineages of + +Athanas + +and + +Salmoneus + +resulted in remarkable convergences between these two genera, for instance, in the shape of the frontal margin of the carapace (decrease in length of the rostrum and reduction of orbital teeth), reduction of the cornea size, strengthening of the antennal flagella, and appearance of either setal brushes ( + +Athanas + +) or setal rows ( + +Salmoneus + +) on the chelae of the first pereiopods. + + +The recent phylogenetic hypothesis for the +Alpheidae +based on molecular data ( + +Chow +et al. +2021 + +) showed a non-monophyly of + +Athanas + +in its present composition (see also discussion under + +Pseudathanas + +). Another important result of this study was the lack of support for the two currently recognised, informal species groups within the genus, which were in use since +Coutière (1899) +, namely the + +A. nitescens +( +Leach, 1814 +) + +group (containing species with extended chelipeds) and the + +A. dimorphus +Ortmann, 1890 + +group (containing species with ventrally folded chelipeds). Therefore, the herein provided diagnosis of + +Athanas + +should be used with some reservation as further taxonomic rearrangements, with redefinitions of genera and their diagnostic features, are expected in the near future. + + +
+
\ No newline at end of file diff --git a/data/38/6A/BE/386ABE42FFB3FFA7FF06AFB32CE0FC9C.xml b/data/38/6A/BE/386ABE42FFB3FFA7FF06AFB32CE0FC9C.xml new file mode 100644 index 00000000000..1344b724c07 --- /dev/null +++ b/data/38/6A/BE/386ABE42FFB3FFA7FF06AFB32CE0FC9C.xml @@ -0,0 +1,469 @@ + + + +Alpheid shrimps of the genera Athanas Leach, 1814, Athanopsis Coutière, 1897 and Pseudathanas Bruce, 1983 of the coasts of the Arabian Peninsula (Malacostraca: Decapoda: Caridea) + + + +Author + +Anker, Arthur +Universidade Federal de Pelotas (UFPEL), Departamento de Ecologia, Zoologia e Genética, Instituto de Biologia, Campus Universitário Capão do Leão, RS, 96010 - 610, Brazil & Red Sea Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia + +text + + +Zootaxa + + +2023 + +2023-12-11 + + +5383 + + +2 + + +179 +215 + + + + +https://www.mapress.com/zt/article/download/zootaxa.5383.2.5/52448 + +journal article +10.11646/zootaxa.5383.2.5 +1175-5326 +10350767 +7E434B40-6346-4E6D-BC55-38EBAE24BD52 + + + + + + + +Athanas claereboudti + +sp. nov. + + + + + + +( +Figs. 1–3 +) + + + + +Material examined +. + +Holotype +: +1 male +(cl 5.0 mm), +FLMNH +UF 71417 +, +Oman +, +Masirah Island +, west coast (channel side), +20°27’44.0”N +/ +58°46’39.8”E +, muddy sandflat with seagrass, depth + +0.5 m + +, suction pump, leg. +A. Anker +, + +08.11.2022 + +[fcn BOMAN-13043] + +. + +Paratypes +: +1 male +(cl +4.9 mm +, missing minor cheliped), +FLMNH +UF 71414 +, same collection data as for holotype [fcn BOMAN-13042] + +; + +1 male +(cl +4.1 mm +, missing major cheliped), +FLMNH +UF 63930 +, +Oman +, east of Muscat, +Bandar Khayran +, +23°30’32.5”N +/ +58°43’53.5”E +, mangrove and adjacent mudflat, at night, depth at low tide + +0–1 m + +, suction pump, in burrow, leg. +A. Anker +, + +04.02.2022 + +[fcn BOMAN-11363] + +. + + + + +Description +. Carapace ( +Fig. 1a–c +) covered with short erect setae, especially dorsally, without post-rostral tubercle. Rostrum ( +Fig. 1b, c +) short, reaching to mid-length of first article of antennular peduncle, subtriangular, with subacute tip; rostral carina absent. Extra-corneal teeth ( +Fig. 1b, c +) reduced to small bumps; infra-corneal teeth absent. Pterygostomial angle ( +Fig. 1c +) rounded, not produced anteriorly. Cardiac notch ( +Fig. 1a +) deep. + + +Pleon ( +Fig. 1d +) mostly glabrous; first to fourth pleura rounded distoventrally; fifth pleonite angular distoventrally; sixth pleonite with subtriangular articulated plate. Telson ( +Fig. 1e +) strongly tapering distally, about 1.8 times as long as proximal width; dorsal surface with two pairs of stout spiniform setae situated at some distance from lateral margins, approximately at 0.35 (anterior) and 0.65 (posterior) of telson length; posterior margin slightly concave, with two pairs of spiniform setae, mesial twice as long as lateral. + + +Eyes ( +Fig. 1b, c +) partly exposed dorsally and laterally, with well pigmented but slightly reduced corneas; anteromesial margin of eyestalks rounded, unarmed. + + +Antennule ( +Fig. 1b, c, f +) moderately stout; stylocerite with acute tip, reaching or slightly overreaching mid-length of second article of peduncle; ventromesial carina with large, anteriorly directed, blunt tooth; second article about 1.3 times as long as wide; lateral flagellum with fused portion composed of five units, accessory ramus well developed, subdivided into four poorly individualised units, each carrying group of three or four aesthetascs. + + +Antenna ( +Fig. 1b, c, g +) with basicerite very stout, its distolateral margin armed with blunt tooth; scaphocerite broad, reaching to end of antennular peduncle; lateral margin straight to faintly convex; blade broadly convex anteriorly, by far overreaching small distolateral tooth; carpocerite very stout, significantly overreaching both antennular peduncle and scaphocerite; flagellum conspicuously thickened. + + +Mouthparts not dissected, typical for genus in external observation. Third maxilliped ( +Fig. 1h +) slender; coxa with somewhat produced, distally subacute lateral plate above mastigobranch; antepenultimate article somewhat curved, tapering distally, about six times as long as maximal width; penultimate article slender, about five times as long as wide; ultimate article slender, twice as long as penultimate article, tapering only apically, with unarmed tip; exopod well developed, about same length as antepenultimate article. + + +First pereiopods (= chelipeds) about 20% unequal in size, asymmetrical in shape, carried folded ventrally when not in use ( +Figs. 2 +, +3 +). Minor cheliped ( +Fig. 2a–d +) robust; basis with rudimentary exopod; ischium stout, somewhat flattened ventrally, widening distally, with one spiniform seta on ventromesial margin and row of four unevenly spaced spiniform setae on dorsal margin; merus greatly swollen, with strongly convex dorsal and ventral margins, about 2.5 times as long as greatest width, excavated ventrally, dorsal margin with small tubercles in distal half, distodorsal surface with conspicuously protruding, slightly curved, blunt process, ventrolateral margin furnished with small teeth, distal-most largest; carpus pear-shaped, narrow proximally, widening distally, ventromesial margin with small lobe, rest of surface and margins smooth; chela slightly longer than merus; palm swollen, depressed ventrolaterally, about twice as long as high (wide) in mesial view of chela, ventral margin with row of small tubercles; fingers about 0.8 times as long as palm, strongly curved, noticeably deviating from axis of palm, slender, with unarmed, blade-like cutting edges. Major cheliped ( +Fig. 2e–h +) robust; basis with rudimentary exopod; ischium stout, somewhat flattened ventrally, widening distally, with row of seven equidistant spiniform setae on dorsal margin, ventrolateral margin rugose, ending distally in subacute tooth; merus less swollen than in minor cheliped, with strongly convex dorsal margin and almost straight ventral margin, about 2.8 times as long as greatest width, excavated ventrally, dorsal margin smooth, distodorsal surface with conspicuously protruding, slightly curved, blunt process similar to that of minor cheliped, ventrolateral margin evenly serrated, i.e., with small rounded teeth; carpus cup-shaped, very short, widening and with blunt lobes distally, smooth; chela distinctly longer than merus; palm swollen, depressed ventrolaterally, about 2.2 times as long as high (wide) in mesial view of chela, ventral margin with row of small tubercles; fingers about half-length of palm, somewhat curved, noticeably deviating from axis of palm, stout, gaping distally; pollex with four stout teeth on cutting edge, with large gap between two distal-most teeth; dactylus with strongly bent tip, cutting edge with two subtriangular teeth, one smaller proximal tooth and one much larger tooth at about 0.4 dactylar length, distal half of dactylus unarmed, concave. + + + +FIGURE 1. + +Athanas claereboudti + + +sp. nov. + +, paratype, male (cl 4.1 mm) from Bandar Khayran, Oman (FLMNH UF 63930), a, carapace, lateral; b, frontal region, dorsal; c, same, lateral; d, posterior portion of pleon and telson, lateral; e, telson, dorsal; f, tooth of ventromesial carina of first article of antennular peduncle, lateral; g, antennal scaphocerite, dorsal; h, third maxilliped, lateral; i, second pereiopod, lateral; j, third pereiopod, lateral; k, fourth pereiopod, lateral; l, fifth pereiopod, lateral; m, appendix masculina and appendix interna of second pleopod, anterior (lateral); n, uropod, dorsal (marginal setae omitted). + + + + +FIGURE 2. + +Athanas claereboudti + + +sp. nov. + +, paratype, male (cl 4.1 mm) from Bandar Khayran, Oman (FLMNH UF 63930) [a–d]; paratype, male (cl 4.9 mm) from Masirah Island, Oman (FLMNH UF 71414) [e–h]; a, left (minor) cheliped, mesial; b, same, lateral; c, same, chela with fingers open, mesial; d, right (major) cheliped, coxa and basis, lateral; e, right (major) cheliped (drawn +in situ +), mesial; f, same, lateral; g, distal portion of merus, carpus and chela, lateral; h, same, chela fingers, lateral. + + + + +FIGURE 3. + +Athanas claereboudti + + +sp. nov. + +, holotype, male (cl 5.0 mm) from Masirah Island, Oman (FLMNH UF 71417); a, shrimp in life, lateral (left side); b, same, lateral (right side); c, same, dorsal. Photographs by the author. + + + +Second pereiopod ( +Fig. 1i +) slender; ischium at most four times as long as maximal width; merus about 1.3 times as long as ischium; carpus with five subarticles, proximal slightly longer than sum of four others; chela longer than distal-most carpal subarticle, simple, with fingers much longer than palm. Third to fifth pereiopods relatively slender, similar in length. Third pereiopod ( +Fig. 1j +) with ischium armed with two spiniform setae on ventrolateral surface; merus about 1.8 times as long as ischium, 5.2 times as long as maximal width, feebly convex dorsally; carpus noticeably more slender than merus, about 0.6 length of merus, with one stiff seta on distoventral margin; propodus about 1.2 times as long as carpus, with two widely spaced, stiff setae on ventral margin and one pair of spiniform setae distally, flanking base of dactylus; dactylus simple, slender, strongly curved in distal half, almost sickle-shaped, about 0.6 length of propodus. Fourth pereiopod ( +Fig. 1k +) generally similar to third pereiopod; ischium armed with two spiniform setae on ventrolateral surface; merus noticeably slenderer than in third pereiopod, 5.8 times as long as maximal width; carpus about 0.6 times as long as merus; propodus with one stiff seta on ventral margin and one pair of spiniform setae distally, flanking base of dactylus; dactylus similar to that of third pereiopod. Fifth pereiopod ( +Fig. 1l +) slenderest of walking legs; ischium with one spiniform seta on ventrolateral surface; merus about twice as long as ischium; carpus almost 0.7 length of merus; propodus distinctly longer than merus, with six rows of microserrulate setae on distolateral surface; dactylus slightly less curved than in third or fourth pereiopods. + + +Uropod ( +Fig. 1n +) with lateral lobe of protopod subacute distally; exopod with small, blunt, distolateral tooth and small adjacent spiniform seta; diaeresis straight for most part; endopod ovoid, slightly shorter and narrower than exopod. + +Gill-exopod formula as given for genus; basis of third maxilliped with rudimentary exopod; mastigobranchs present on coxae of third maxilliped and first to third pereiopods; setobranchs present on coxae of first to fourth pereiopods. + +Colour in life +. Background hyaline whitish with slight yellowish tinge; carapace and pleon largely covered by irregular blotches of red chromatophores; mid-dorsal line of carapace, pleon and entire telson without red chromatophores, instead with patches of buff white chromatophores; carapace flanks and ventral surface of anterior pleonites mostly colourless; antennular and antennal peduncles patchily covered with red chromatophores, flagella whitish; chelipeds hyaline white with occasional red blotch on merus; remaining pereiopods and pleopods whitish; uropods with blotches of red chromatophores ( +Fig. 3 +). + + + + +Etymology +. The species is named after Dr. Michel Claereboudt (formerly at Sultan Qaboos University, +Muscat +, +Oman +) for his invaluable help in the organisation of the +Oman +BioBlitz expedition series. + + + + + + +Type +locality + +. +Masirah Island +, +Oman + +. + + + + +Distribution +. Currently known only from two localities in +Oman +: Masirah Island and Bandar Khayran east of +Muscat +. + + + + +Ecology +. All +three specimens +were collected from burrows of unknown hosts on very shallow (less than +1 m +) subtidal mudflats or muddy sandflats, close to mangroves (Bandar Khayran) or seagrass beds (Masirah). The larger syntopic infauna, which is still being sorted and studied, includes large burrowing snapping shrimps ( + +Alpheus +spp. + +, including + +A. +aff. +djeddensis +Coutière, 1897 + +), callianassid ghost-shrimps, upogebiid mud-shrimps and stomatopods. + + + + +Remarks +. + +Athanas claereboudti + + +sp. nov. + +possesses a unique and conspicuous character not found in any other member of the genus + +Athanas + +. The merus of both the major and the minor cheliped of + +A. claereboudti + + +sp. nov. + +presents a very prominent, blunt, somewhat curved process in its distodorsal part ( +Fig. 2a, b, e, g +). The overall combination of morphological characters of the new species, especially those of the frontal region and chelipeds, suggests that it may be most closely related to + +A. iranicus +Anker, Naderloo & Marin, 2010 + +, + +A. daviei +Anker, 2011 + +, and + +A. manticolus +Ďuriš & Anker 2014 + +, all of them also being infaunal, symbiotic species (Anker +et al +. 2010; +Anker 2011b +; +Ďuriš & Anker 2014 +). However, + +A. claereboudti + + +sp. nov. + +can be easily separated from each of the three aforementioned species by at least three morphological characters, in addition to the bulging distodorsal process on the cheliped meri. For instance, + +A. claereboudti + + +sp. nov. + +differs from + +A. iranicus + +by the absence of setal brushes on the carpus and chela (which are characteristic of + +A. iranicus + +, see also below); the posterior margin of the telson slightly concave ( +vs +. broadly rounded in + +A. iranicus + +); and the antennal scaphocerite reaching or very slightly overreaching the end of the antennular peduncle ( +vs. +reaching far beyond it in + +A. iranicus + +) (cf. +Figs. 2e–h +; Anker +et al +. 2010: figs. 2B, E, 3A, B, E). Similarly, the new species differs from + +A. daviei + +by the noticeably shorter rostrum; the longer stylocerite; the much more swollen cheliped meri; and the slenderer second pereiopod (cf. +Figs. 1 +, +2a, b +; Anker 2011: figs. 3A, 4A, B, D–F). Finally, + +A. claereboudti + + +sp. nov. + +can be easily separated from + +A. manticolus + +by the dorsally non-dentate rostrum; the absence of postrostral tubercle; and the more unequal and asymmetrical chelipeds, each with a much more swollen merus (cf. +Figs. 2 +, +3 +; +Ďuriš & Anker 2014 +: figs. 2A, C, 4). In addition, + +A. claereboudti + + +sp. nov. + +can be distinguished from + +A. iranicus + +, + +A. daviei + +and + +A. manticolus + +by its diagnostic colour pattern (cf. +Figs. 3 +, +5 +, Anker 2011: fig. 8E, F; +Ďuriš & Anker 2014 +: fig. 6A, B). All other known species of + +Athanas + +, including all infaunal species, present more significant morphological differences with + +A. claereboudti + + +sp. nov. + +and (where known) also differ from the new species by their colour patterns (e.g., +Hayashi 2002 +; +Anker & Komai 2010 +; +Anker 2011b +; +Marin 2017 +; +Anker & Ďuriš 2022 +). + + + + \ No newline at end of file diff --git a/data/38/6A/BE/386ABE42FFB8FFA5FF06ADC72CC3FC48.xml b/data/38/6A/BE/386ABE42FFB8FFA5FF06ADC72CC3FC48.xml new file mode 100644 index 00000000000..7e4ca55773c --- /dev/null +++ b/data/38/6A/BE/386ABE42FFB8FFA5FF06ADC72CC3FC48.xml @@ -0,0 +1,445 @@ + + + +Alpheid shrimps of the genera Athanas Leach, 1814, Athanopsis Coutière, 1897 and Pseudathanas Bruce, 1983 of the coasts of the Arabian Peninsula (Malacostraca: Decapoda: Caridea) + + + +Author + +Anker, Arthur +Universidade Federal de Pelotas (UFPEL), Departamento de Ecologia, Zoologia e Genética, Instituto de Biologia, Campus Universitário Capão do Leão, RS, 96010 - 610, Brazil & Red Sea Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia + +text + + +Zootaxa + + +2023 + +2023-12-11 + + +5383 + + +2 + + +179 +215 + + + + +https://www.mapress.com/zt/article/download/zootaxa.5383.2.5/52448 + +journal article +10.11646/zootaxa.5383.2.5 +1175-5326 +10350767 +7E434B40-6346-4E6D-BC55-38EBAE24BD52 + + + + + + + +Athanas +cf. +dentirostris +Anker, Jeng & Chan, 2001 + + + + + + + +( +Fig. 4 +) + + + + + + + +Athanas dentirostris + +Anker +et al. +2001: 1049 + + + +, figs. 1–3. + + + + + +Material examined +. + +1 male +(cl +4.4 mm +), +FLMNH +UF 71432 +, +Oman +, +Masirah Island +, channel side, +Dafiyat +, +20°35’15.1”N +/ +58°49’36.9”E +, intertidal and shallow subtidal sandflat with patches of coral rubble, rocks and seagrass, depth at low tide less than + +0.5 m + +, suction pump, in burrow, leg. +A. Anker +, + +08.11.2022 + +[fcn BOMAN-13044] + +; + +1 male +(cl +3.5 mm +), 1 ovig. female (cl 4.0 mm), +FLMNH +UF 71419 +, same collection data as for previous specimen [fcn BOMAN-13052]; 1 ovig. female (cl +3.6 mm +), +FLMNH +UF 71434 +, same collection data as for previous specimens [fcn BOMAN-13051] + +; + +3 females +(incl. 2 ovig., cl not measured, all missing major chelipeds), +FLMNH +UF 71438 +, same collection data as for previous specimens [fcn BOMAN-13053] + +; + +1 male +(cl +3.6 mm +, missing both chelipeds), +FLMNH +UF 71433 +, same collection locality as for previous specimens, leg. +A. Anker +, + +13.11.2022 + +[fcn BOMAN-13817]; 1 ovig. female (cl +4.7 mm +), +FLMNH +UF 71415 +, same collection data as for previous specimen [fcn BOMAN-13826]; 1 ovig. female (cl +4.6 mm +), +FLMNH +UF 71416 +, same collection data as for previous specimen [fcn BOMAN-13825] + +; + +4 females +(incl. 3 ovig., all but one without chelipeds), +FLMNH +UF 71436 +, same collection data as for previous specimen [fcn BOMAN-13827] + +; + +1 male +(cl 5.0 mm), +FLMNH +UF 71430 +, same collection data as for previous specimen [fcn BOMAN-13824] + +; + +1 male +(cl 5.0 mm), +FLMNH +UF 71431 +, same collection data as for previous specimens [fcn BOMAN-13837] + +; + +1 male +(cl +4.7 mm +), 2 ovig. females (cl +3.9 mm +, 4.0 mm, former missing both chelipeds), +FLMNH +UF 71413 +, same collection data as for previous specimens [fcn BOMAN-13814] + +; + +1 male +(cl +5.3 mm +), +FLMNH +UF 71421 +, same collection data as for previous specimens [fcn BOMAN-13823] + +; + +1 male +(cl +5.1 mm +), +FLMNH +UF 71439 +, same collection locality as for previous specimens, leg. +A. Anker +, + +15.11.2022 + +[fcn BOMAN-14056] + +; + +1 male +(cl +4.8 mm +), +FLMNH +UF 71435 +, same collection data as for previous specimen [fcn BOMAN-14062] + +; + +1 male +(cl +2.9 mm +), +FLMNH +UF 71420 +, same collection data as for previous specimen [fcn BOMAN-14053] + +. + + + + +Description +. For description and illustrations of + +A. dentirostris + +see + +Anker +et al. +(2001) + +; some taxonomic remarks on the Omani material tentatively identified herein as + +A. +cf. +dentirostris + +are provided below, including description and illustration of the shrimps’ conspicuous colour pattern ( +Fig. 4 +). + + + +FIGURE 4. + +Athanas +cf. +dentirostris +Anker, Jeng & Chan, 2001 + +, male (cl 4.4 mm) from Masirah Island, Oman (FLMNH UF 71432); a, shrimp in life, lateral (right side); b, same, lateral (left side); c, same, dorsal. Photographs by the author. + + + +Colour in life +. Background translucent whitish; carapace and pleon irregularly speckled with numerous, large, dark red dots, each composed of several red chromatophores; some white chromatophores interspersed among red ones, forming large star-shaped patches; dorsal surface of carapace and pleon with larger transverse bands formed by white chromatophores, most conspicuous on third and fourth pleonites; telson with proximal half translucent with red dots and distal half conspicuously white; antennular and antennal peduncles mostly covered with red dots, flagella with scarce red dots proximally, colourless distally; third maxillipeds and second pereiopods whitish with red dots; chelipeds hyaline white with patches of red dots, denser on merus and chelae, carpus additionally with some white patches, fingers ivory white; remaining pereiopods mostly colourless; uropods with endopod and proximal and central portion of exopod translucent with red dots, distal portion with conspicuous white patch ( +Fig. 4 +). + + + + +Distribution +. +Vietnam +: Cua Luc ( +type +locality of + +A. dentirostris + +) ( + +Anker +et al. +2001 + +); possibly +Oman +: Masirah Island ( + +A. +cf. +dentirostris + +) (present study). + + + + +Ecology +. All specimens of + +A. +cf. +dentirostris + +were collected from burrows in the sandy-muddy intertidal or the adjacent shallow subtidal (less than +1 m +), with large patches of seagrass. The syntopic infauna, which is still being studied, included large snapping shrimps ( + +Alpheus +spp. + +) and upogebiid mud-shrimps. At least +two specimens +of + +A. +cf. +dentirostris + +were collected from burrows together with the snapping shrimp + +Alpheus +cf. +lobidens +De Haan, 1849 + +, in the muddier part of the intertidal. The +holotype +of + +A. dentirostris + +was collected, according to the specimen label, together with + +Austinogebia +aff. +takaoensis + +(Sakai & Türkay, 1995) “in fine mud and grit” (Anker +et al. +2021). + + + + +Remarks +. + +Athanas dentirostris + +is presently known with certainty only from the +holotype +from northern +Vietnam +( + +Anker +et al. +2001 + +). The abundant Omani material may well be conspecific with + +A. dentirostris + +or represent a closely related species. The dorsal teeth of the rostrum appear to be more pronounced in the Omani material of + +A. +cf. +dentirostris + +compared to those of the +holotype +of + +A. dentirostris + +. In fact, in some Omani specimens, the distal-most teeth are very conspicuous and more closely positioned to each other, compared to the smaller and more widely spaced teeth of the +holotype +. Furthermore, the armature of the finger cutting edges of the major chela of the Omani male specimens appears to be stronger than in the Vietnamese male +holotype +, with one some teeth also present on the dactylus. The cutting edge of the major chela dactylus was illustrated as unarmed in Anker +et al. +(2021: fig. 3c); however, it must be noted that the cutting edges and adjacent areas of both fingers are largely concealed by a dense setal cover. In all other important details, the Omani specimens seem to correspond well to the +holotype +of + +A. dentirostris + +. Since no intraspecific variation can be presently assessed for the Vietnamese population of + +A. dentirostris + +and considering the significantly smaller size of the +holotype +male (cl +3.8 mm +) compared to the largest males from Masirah Island (cl 5.0– +5.2 mm +), which may explain differences in the cheliped armature, the author prefers to report the Omani material as + +A. +cf. +dentirostris + +. The collection of more material of + +A. dentirostris + +in +Vietnam +and across South-East Asia is needed to solve the identity of + +A. +cf. +dentirostris + +, which may also involve comparisons of DNA sequences and colour patterns. + + + + \ No newline at end of file diff --git a/data/38/6A/BE/386ABE42FFBAFFA3FF06AA732A6DFD68.xml b/data/38/6A/BE/386ABE42FFBAFFA3FF06AA732A6DFD68.xml new file mode 100644 index 00000000000..81da9943944 --- /dev/null +++ b/data/38/6A/BE/386ABE42FFBAFFA3FF06AA732A6DFD68.xml @@ -0,0 +1,365 @@ + + + +Alpheid shrimps of the genera Athanas Leach, 1814, Athanopsis Coutière, 1897 and Pseudathanas Bruce, 1983 of the coasts of the Arabian Peninsula (Malacostraca: Decapoda: Caridea) + + + +Author + +Anker, Arthur +Universidade Federal de Pelotas (UFPEL), Departamento de Ecologia, Zoologia e Genética, Instituto de Biologia, Campus Universitário Capão do Leão, RS, 96010 - 610, Brazil & Red Sea Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia + +text + + +Zootaxa + + +2023 + +2023-12-11 + + +5383 + + +2 + + +179 +215 + + + + +https://www.mapress.com/zt/article/download/zootaxa.5383.2.5/52448 + +journal article +10.11646/zootaxa.5383.2.5 +1175-5326 +10350767 +7E434B40-6346-4E6D-BC55-38EBAE24BD52 + + + + + + + +Athanas iranicus +Anker, Naderloo & Marin, 2010 + + + + + + + +( +Fig. 5 +) + + + + + + +Athanas iranicus +Anker +et al. +2010: 54 + +, figs. 1–4; Naderloo & Türkay 2012: 12; + + +Ashrafi +et al +. 2020a: 520 + + +( +Table 1 +). + + + + + +Material examined +. + +1 female +(cl +3.6mm +), +FLMNH +UF68857 +, +Oman +, east of Muscat, +Bandar Khayran +, +23°30’32.3”N +/ +58°43’58.0”E +, mangrove, muddy sand and mud, depth + +0–1 m + +, suction pump, in burrow, leg. +A. Anker +et al +., + +01.02.2022 + +[fcn BOMAN-09986] + +; + +1 female +(cl +2.8 mm +), +FLMNH +UF 68860 +, same collection data as for previous specimen [fcn BOMAN-09985]; 1 ovig. female (cl +3.6 mm +), +FLMNH +UF 68858 +, +Oman +, east of Muscat, +Bandar Khayran +, +23°30’32.5”N +/ +58°43’53.5”E +, mangrove and adjacent mudflat, at night, depth at low tide + +0–1 m + +, suction pump, in burrow, leg. +A. Anker +, + +04.02.2022 + +[fcn BOMAN-11371] + +; + +1 female +(cl +2.5 mm +), +FLMNH +UF 68861 +, same collection data as for previous specimen [fcn BOMAN-11355] + +. + + + + +Description +. See Anker +et al. +(2010) for description and illustrations; some taxonomic remarks on the Omani material are provided below, whereas the species’ colour pattern is described and illustrated for the first time ( +Fig. 5 +). + + +Colour in life +. Background semi-opaque whitish; carapace and pleon speckled with numerous blotches of red chromatophores, except for large part of branchial area of carapace; dorsal surface of carapace, including rostral and post-rostral area, with large patches of buff white chromatophores; pleon with broad mid-dorsal band of buff white colour stretching from anterior margin of first pleonite to posterior margin of sixth pleonite, and extending as transverse bands on first, third, fourth (slightly) and sixth (forming large transverse patch) pleonites; some red chromatophores visible within buff white mid-dorsal band or patches on carapace and pleon; telson with proximal two-thirds bright red and distal one-third conspicuously yellowish white; antennular peduncle with bright red chromatophores on stylocerite and some parts of first article, and bright yellow white chromatophores on most of remaining peduncle and proximal flagella; antennae largely translucent with bright red chromatophores on scaphocerite and carpocerite, distal area of scaphocerite yellow white, flagellum colourless; major cheliped hyaline white with patches of red chromatophores, especially on chela; minor cheliped and remaining pereiopods, as well as pleopods, mostly whitish; uropods with proximal half deep red and distal half conspicuously yellowish white (similar to telson); eggs red orange ( +Fig. 5 +). + + + + +Distribution +. +Iran +: +Qeshm Island +(Anker +et al +. 2010); +Oman +: Bandar Khayran east of +Muscat +(present study). + + + + +Ecology +. The four Omani specimens of + +A. iranicus + +were collected in muddy mangrove channels from burrows of unknown hosts. The syntopic macrofauna included large burrowing snapping shrimps ( + +Alpheus +spp. + +) and their associates (e.g., + +Salmoneus rostratus +Barnard, 1962 + +), several species of fossorial crabs ( + +Macrophthalmus +spp. + +), and callianassid ghost-shrimps. The +holotype +from +Iran +was collected, according to the label accompanying the specimen, in “muddy sand with shell fragments” (Anker +et al. +2010). + + + + +FIGURE 5. + +Athanas iranicus +Anker, Naderloo & Marin, 2010 + +, ovigerous female (cl 3.6 mm) from Bandar Khayran, Oman (FLMNH UF 68858); a, shrimp in life, right antennal flagellum broken, dorsal; b, same, lateral (left side). Photographs by the author. + + + + +Remarks +. + +Athanas iranicus + +is a distinctive member of the genus + +Athanas + +, due to its unique combination of morphological features. Especially diagnostic for + +A. iranicus + +are the very short rostrum; the greatly reduced orbital teeth; the robust, somewhat unequal and assymmetrical chelipeds, which are furnished with dense fields of fine setae, one extending from the carpus to the proximal portion of the propodus and one on the fingers; and the relatively robust walking legs (Anker +et al. +2010). The species was hitherto known only from the type locality in +Iran +( +Qeshm Island +north of Strait of +Hormuz +) and based on a single male +holotype +. The material from Bandar Khayran represents the second only finding of + +A. iranicus + +and extends the previously known distribution range of the species from +Iran +to +Oman +. It is likely that + +A. iranicus + +is more widely distributed in the north-western Indian Ocean, although it has not been collected at other sampled localities along the eastern and southern coasts of +Oman +( +Dhofar +and Masirah Island) (A. Anker, pers. obs.). + + +All Omani specimens of + +A. iranicus + +are females, including one ovigerous female ( +Fig. 5 +). They present no significant discrepancies from the description of the male +holotype +. In all but +one specimen +, the chelae possess two distinct areas of fine dense setae, as described above; these setae are only missing (or at least are very poorly developed) in the smallest female (cl +2.5 mm +) (FLMNH UF 68861). The previously unknown colour pattern of + +A. iranicus + +( +Fig. 5 +) is most similar to the colour patterns of + +A. shawnsmithi +Anker, 2011 + +, + +A. daviei +Anker, 2011 + +(cf. Anker 2011: fig. 8A–F; Anker +et al. +2015: fig. 9) and the above-described + +A. claereboudti + + +sp. nov. + +( +Fig. 3 +). On the other hand, the stomatopod-associated species + +A. ahyongi +Anker & Komai, 2010 + +, + +A. manticolus +Ďuriš & Anker, 2014 + +and + +A. philippei +Anker & Ďuriš 2022 + +, as well as the + +Alpheus + +-associated + +A. alpheusophilus +Marin, 2017 + +and the above-reported + +A. +cf. +dentirostris + +, have very different colour patterns (cf. +Fig. 4 +; +Anker & Komai 2010 +: fig. 6; +Ďuriš & Anker 2014 +: fig. 6; +Marin 2017 +: fig. 6; +Anker & Ďuriš 2022 +: figs. 5, 6A, B). + + + + \ No newline at end of file diff --git a/data/38/6A/BE/386ABE42FFBCFFA3FF06AD532AE7F8F3.xml b/data/38/6A/BE/386ABE42FFBCFFA3FF06AD532AE7F8F3.xml new file mode 100644 index 00000000000..db17bcb2ace --- /dev/null +++ b/data/38/6A/BE/386ABE42FFBCFFA3FF06AD532AE7F8F3.xml @@ -0,0 +1,295 @@ + + + +Alpheid shrimps of the genera Athanas Leach, 1814, Athanopsis Coutière, 1897 and Pseudathanas Bruce, 1983 of the coasts of the Arabian Peninsula (Malacostraca: Decapoda: Caridea) + + + +Author + +Anker, Arthur +Universidade Federal de Pelotas (UFPEL), Departamento de Ecologia, Zoologia e Genética, Instituto de Biologia, Campus Universitário Capão do Leão, RS, 96010 - 610, Brazil & Red Sea Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia + +text + + +Zootaxa + + +2023 + +2023-12-11 + + +5383 + + +2 + + +179 +215 + + + + +https://www.mapress.com/zt/article/download/zootaxa.5383.2.5/52448 + +journal article +10.11646/zootaxa.5383.2.5 +1175-5326 +10350767 +7E434B40-6346-4E6D-BC55-38EBAE24BD52 + + + + + + + +Athanas minikoensis +Coutière, 1903 + + + + + + + +( +Fig. 6 +) + + + + + + + +Athanas Minikoensis +Coutière 1903: 76 + + +, figs. 9–11; + +Coutière 1905: 858 + +, fig. 130; + +De Man 1911: 149 + +, (1915) pl. 2, fig. 5. + + + + + +Athanas minikoensis +— + + +Ramadan 1936: 13 + +; (?) + +Fourmanoir 1958: 126 + +, fig. 15; (?) +Macnae & Kalk 1969: 43 +; + +Kensley 1970: 118 + +, fig. 12; + +Kensley 1972: 54 + +, fig. 25j; + +Kensley 1981: 26 + +; + +Banner & Banner 1981: 43 + +; + +Banner & Banner 1983: 81 + +; + +Banner & +Banner 1985: 34 + +. + + + + +(?) + +Athanas +cf. +minikoensis + +— + +Barnard 1947: 388 + +; + +Barnard 1950: 731 + +, fig. 137a–d. + + + + + +Material examined +. + +1 ovig. female (cl +3.2 mm +), +FLMNH +UF 71422 +, +Oman +, +Masirah Island +, +2 km +north of +Ghab +, +20°15’51.6”N +/ +58°37’26.3”E +, coral reef flat, fragmenting of coral rubble, depth + +1.5 m + +, leg. +A. Anker +, + +20.11.2022 + +[fcn BOMAN-14832] + +. + + + + +Description +. For description and illustrations of + +A. minikoensis + +see +Coutière (1903 +, +1905 +), +De Man (1911) +, +Barnard (1950 +, as + +A. +cf. +minikoensis + +, with some reservation) and +Kensley (1970) +; colour pattern of the single Omani female specimen herein identified as + +A. minikoensis + +is described below and shown in +Fig. 6 +. + + +Colour in life +. Background largely translucent; mid-dorsal surface with broad longitudinal band formed by buff white chromatophores and expanding laterally near mid-length of carapace and each pleonite in trapezoid pattern; each anterolateral margin of carapace with red broad reddish band descending from each eye towards pterygostomial region; pleon with scattered red chromatophores, most disposed in chains; chelipeds hyaline white; remaining pereiopods, pleopods and tail fan largely colourless ( +Fig. 6 +). + + + + +Distribution +. Indo-West Pacific from the Red Sea and +South Africa +(as + +A. +cf. +minikoensis + +) to +Papua New Guinea +( +Coutière 1903 +, +1905 +; +De Man 1911 +; +Ramadan 1936 +; +Barnard 1950 +; +Kensley 1970 +, +1972 +; +Banner & Banner 1981 +, +1983 +, +1985 +); apparently first record from +Oman +(present study). + + + + +Ecology +. Poorly known, however, appears to be bound to coral reef habitats ( +De Man 1911 +). The single Omani specimen was collected by breaking pieces of coral rubble into a sieve at a depth of about +1.5 m +. + + + + +Remarks +. The single ovigerous female from Masirah Island was identified as + +A. minikoensis + +based mainly on the configuration of the fronto-orbital region, especially the enlarged, protruding extra-orbital teeth, the much smaller infra-orbital teeth, the absence of supra-corneal teeth, as well as the asymmetrical chelipeds carried folded beneath the body ( +Fig. 6 +). Despite being widespread in the Indo-West Pacific, + +A. minikoensis + +is not well known morphologically and ecologically ( +De Man 1911 +; +Barnard 1950 +; +Kensley 1970 +). More material, especially fully grown and complete males, are needed to confirm the present record of the species from +Oman +. + + + + \ No newline at end of file diff --git a/data/38/6A/BE/386ABE42FFBEFFA0FF06AEDA2D0BFD0C.xml b/data/38/6A/BE/386ABE42FFBEFFA0FF06AEDA2D0BFD0C.xml new file mode 100644 index 00000000000..914171d729d --- /dev/null +++ b/data/38/6A/BE/386ABE42FFBEFFA0FF06AEDA2D0BFD0C.xml @@ -0,0 +1,259 @@ + + + +Alpheid shrimps of the genera Athanas Leach, 1814, Athanopsis Coutière, 1897 and Pseudathanas Bruce, 1983 of the coasts of the Arabian Peninsula (Malacostraca: Decapoda: Caridea) + + + +Author + +Anker, Arthur +Universidade Federal de Pelotas (UFPEL), Departamento de Ecologia, Zoologia e Genética, Instituto de Biologia, Campus Universitário Capão do Leão, RS, 96010 - 610, Brazil & Red Sea Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia + +text + + +Zootaxa + + +2023 + +2023-12-11 + + +5383 + + +2 + + +179 +215 + + + + +https://www.mapress.com/zt/article/download/zootaxa.5383.2.5/52448 + +journal article +10.11646/zootaxa.5383.2.5 +1175-5326 +10350767 +7E434B40-6346-4E6D-BC55-38EBAE24BD52 + + + + + + + +Athanas parvus +De Man, 1910 + + + + + + + +( +Fig. 7 +) + + + + + + + +Athanas parvus +De Man, 1910: 315 + + +; + +De Man 1911: 148 + +, (1915) pl. 1, fig. 4; + +Tattersall, 1921: 372 + +; + +Ledoyer, 1970: 126 + +, fig. 11; + + + + +Al-Kandari +et al. +2020: 257 + +, fig. 4. + +Athanas Sibogae +De Man 1910: 314 + +; +De Man 1911: 151 +, (1915) pl. 2, fig. 6. + +Athanas sibogae +— + +Banner & Banner 1973: 321 +, fig. 9; +Banner & Banner 1981: 43 +; +Titgen 1982: 80 +; +Banner & Banner 1983: + + + +81. (Note: selective synonymy, with focus on important morphological accounts and records from the western Indian Ocean) + + + +Material examined +. + +1 male +(cl +2.9 mm +), +FLMNH +UF 71418 +, +Oman +, +Masirah Island +, +2 km +north of +Ghab +, +20°15’51.6”N +/ +58°37’26.3”E +, coral reef flat, under coral rubble on sand, hand collecting, depth + +1.5–2 m + +, leg. +A. Anker +, + +20.11.2022 + +[fcn BOMAN-14839] + +. + + + + +Description +. For description and illustrations of + +A. parvus + +see, for instance, +De Man (1910 +, +1911 +), +Miya & Miyake (1968) +and +Banner & Banner (1973) +; see also +Fig. 7 +. + + + +FIGURE 7. + +Athanas parvus +De Man, 1910 + +, male (cl 2.9 mm) from Masirah Island, Oman (FLMNH UF 71418); a, shrimp in life, lateral (left side); b, dorsal. Photographs by the author. + + + +Colour in life +. Body evenly speckled with bright red chromatophores, carapace and pleon with broad, somewhat nerve cord-shaped band composed of bright white and pinkish white chromatophores, extending along mid-dorsal surface from tip of the rostrum to posterior margin of sixth pleonite; antennular peduncles with large white patches; antenna mostly translucent with red spots; chelipeds hyaline with red spotting; remaining pereiopods mostly translucent with occasional red spotting; tail fan bright red ( +Fig. 7 +). See also + +Al-Kandari +et al. +(2020 + +: fig. 4). + + + + +Distribution +. Indo-West Pacific from the Red Sea and +Madagascar +to +Japan +, +Australia +and +Samoa +( +De Man 1911 +; +Miya & Miyake 1968 +; +Banner & Banner 1973 +, +1985 +; +Chace 1988 +; Anker 2001; +Anker & De Grave 2016 +; + +Al-Kandari +et al. +2020 + +); apparently first record from +Oman +(present study). + + + + +Ecology +. Commonly encountered under rocks, living and dead corals, or in coral crevices, from the lower intertidal to at least +70 m +( +Miya & Miyake 1968 +). + + + + +Remarks +. + +Athanas parvus + +is one of the most common species of the genus, found throughout the Indo-West Pacific. The species can be identified using the combination of the colour pattern ( +Fig. 7 +) with the enlarged, ventrally folding chelipeds, and the presence of biunguiculate dactylus on the third to fifth pereiopods. However, no phylogeographic studies on + +A. parvus + +, including comparison of the populations from the western Indian Ocean with those from the western Pacific have been performed so far. + + + + \ No newline at end of file diff --git a/data/38/6A/BE/386ABE42FFBFFFBFFF06ACB72AD3FD51.xml b/data/38/6A/BE/386ABE42FFBFFFBFFF06ACB72AD3FD51.xml new file mode 100644 index 00000000000..df575b1e474 --- /dev/null +++ b/data/38/6A/BE/386ABE42FFBFFFBFFF06ACB72AD3FD51.xml @@ -0,0 +1,244 @@ + + + +Alpheid shrimps of the genera Athanas Leach, 1814, Athanopsis Coutière, 1897 and Pseudathanas Bruce, 1983 of the coasts of the Arabian Peninsula (Malacostraca: Decapoda: Caridea) + + + +Author + +Anker, Arthur +Universidade Federal de Pelotas (UFPEL), Departamento de Ecologia, Zoologia e Genética, Instituto de Biologia, Campus Universitário Capão do Leão, RS, 96010 - 610, Brazil & Red Sea Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia + +text + + +Zootaxa + + +2023 + +2023-12-11 + + +5383 + + +2 + + +179 +215 + + + + +https://www.mapress.com/zt/article/download/zootaxa.5383.2.5/52448 + +journal article +10.11646/zootaxa.5383.2.5 +1175-5326 +10350767 +7E434B40-6346-4E6D-BC55-38EBAE24BD52 + + + + + + +Genus + +Athanopsis +Coutière, 1897 + + + + + + + + + + +Athanopsis +Coutière 1897: 301 + + +. + + + + + +Emended diagnosis +. Body not compressed, not particularly slender. Carapace smooth, unarmed dorsally and laterally, occasionally with small postrostral tubercle. Rostrum broadly triangular in dorsal view, often narrowing distally, unarmed dorsally and ventrally; tip rounded or truncate in lateral view. Orbital teeth present, small, bluntly triangular. Pterygostomial angle rounded, not protruding; branchiostegite with scarce setae; cardiac notch well developed. All pleonites with distoventrally rounded pleura; sixth pleuron with articulated plate. Telson broad, with two pairs of small to minute spiniform setae on dorsal surface; posterior margin rounded, with two pairs of spiniform setae; anal tubercles absent. Eyes well developed, partly visible or concealed in dorsal view; cornea slightly reduced but well pigmented. Antennular peduncle stout, short; stylocerite well developed, distally blunt or subacute, overreaching distal margin of first article, sometimes exceeding distal margin of second article; ventromesial carina armed with strong tooth; second article short, subquadrate; lateral flagellum with short fused portion and well-developed accessory ramus with aesthetascs. Antenna with basicerite stout, armed with small, sharp tooth; scaphocerite with broad blade and stout distolateral tooth. Mandible with two-articulated palp; molar and incisor processes well developed. Third maxilliped with well-developed exopod; coxa with acutely produced lateral plate; ultimate article tapering into corneous tip, latter usually armed with some spiniform or stiff setae. First pereiopods (= chelipeds) enlarged in both sexes, typically unequal in size and asymmetrical in shape, sometimes subequal and subsymmetrical, carried flexed beneath body when not in use; ischium robust, with dorsal margin typically armed with spiniform setae; merus with smooth margins, ventral surface deeply excavated; carpus short, cup-shaped, without setal rows on mesial surface; chelae usually greatly swollen; palm with or without small tubercles and setal brushes on ventral surface or fingers; fingers of major chela armed with variously shaped teeth, without snapping mechanism. Second pereiopod with ischium unarmed; carpus with five subarticles; chela simple, without modifications. Third and fourth pereiopods moderately stout; ischium armed with typically two spiniform setae; merus unarmed or armed with spiniform setae, its distolateral margin often projecting as subacute tooth; propodus with several spiniform setae; dactylus simple, conical. Fifth pereiopod with ischium unarmed or armed with one spiniform seta; merus with or without spiniform setae; propodus with spiniform setae and short cleaning brush; dactylus simple. Second male pleopod with appendix masculina shorter or subequal in length to appendix interna; second female pleopod with appendix interna only. Uropodal protopod with enlarged, distally produced lateral lobe; exopod with diaeresis straight for most part, unarmed. Gill-exopod formula provided in +Table 2 +. + + + +TABLE 2 +. Gill-exopod formula of + +Athanopsis +Coutière, 1897 + +. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Gills/exopodsMaxillipedsPereiopods
Mxp1Mxp2Mxp3P1P2P3P4P5
Pleurobranchs---+++++
Arthrobranchs--------
Podobranchs--------
Epipods+++1-----
Mastigobranchs2--++++--
Setobranchs---++++-
Exopods++++3/-----
+
+ +1, 2, 3 + +same remarks as for Table 1. + +Species included +. +Type +species + +A. platyrhynchus +Coutière 1897 + +; + +A. dentipes +Miya, 1980 + +; + +A. brevirostris +Banner & Banner, 1981 + +; + +A. australis +Banner & Banner, 1982 + +; + +A. rubricinctuta +Berggren, 1991 + +; + +A. saurus +Anker 2011 + +; + +A. gotoi +Anker, 2012 + +; + +A. tarahomii +Marin, Sheibani & Sari, 2014 + +; + +A. dawa + + +sp. nov. + +(described below). + +
+
+
\ No newline at end of file diff --git a/data/38/6B/23/386B23F399D946344CA6E9381F00422F.xml b/data/38/6B/23/386B23F399D946344CA6E9381F00422F.xml new file mode 100644 index 00000000000..b586ba7796e --- /dev/null +++ b/data/38/6B/23/386B23F399D946344CA6E9381F00422F.xml @@ -0,0 +1,116 @@ + + + +Synopsis of Central Andean Orthalicoid land snails (Gastropoda, Stylommatophora), excluding Bulimulidae + + + +Author + +Breure, Abraham S. H. + + + +Author + +Avila, Valentin Mogollon + +text + + +ZooKeys + + +2016 + +588 + + +1 +199 + + + + +http://dx.doi.org/10.3897/zookeys.588.7906 + +journal article +http://dx.doi.org/10.3897/zookeys.588.7906 +1313-2970-588-1 +EC4E9A71F7B948D2B245F8DA8C0907FA + + + +Taxon classification Animalia Stylommatophora Megaspiridae + + + +Thaumastus (Thaumastus) insolitus (Preston, 1909) +Figs 25 +D-E +, 35 + + + + + +Bulimus +(Thaumastus) insolitus + +Preston 1909 +: 509, pl. 10 fig. 9; +Breure and Ablett 2015 +: 35, 4 +i-iii +, L9ii. + + +Thaumastus insolitus +; +Richardson 1995 +: 377 (references). + + +Thaumastus (Thaumastus) insolitus +; + +Ramirez +et al. 2003 + +: 282. + + + +Type locality. +"Chanchamayo, Peru". + + +Type material. +NHMUK 1947.3.11.1, holotype. + + +Diagnosis. +Shell relatively medium-sized, blackish-brown coloured, coarsly sculptured with transverse ridges crossed by fine, spiral grooves, giving the last whorls a finely beaded appearance, suture somewhat descending in front, peristome thickened, reflexed below, parietal callus polished. + + +Dimensions. +Shell height 70.4, diameter 31.2 mm. + + +Distribution. + +Peru, Dept. +Junin +, Chanchamayo valley; ibid., near Campanillayoc ( +Zilch 1954 +: 76); near Carpapata ( +Breure 1978 +). + + + +Ecoregion. +Peruvian Yungas [NT0153]. + + + \ No newline at end of file diff --git a/data/38/6B/7E/386B7E93AC885A249B6D66C58A41FBBD.xml b/data/38/6B/7E/386B7E93AC885A249B6D66C58A41FBBD.xml new file mode 100644 index 00000000000..00c5c029eff --- /dev/null +++ b/data/38/6B/7E/386B7E93AC885A249B6D66C58A41FBBD.xml @@ -0,0 +1,113 @@ + + + +The terrestrial microsnail genus Aulacospira Moellendorff, 1890 (Eupulmonata, Stylommatophora, Hypselostomatidae) in Thailand with key to Thai species + + + +Author + +Dumrongrojwattana, Pongrat +Department of Biology, Faculty of Science, Burapha University, Bangsaen, Chonburi 20131 Thailand +https://orcid.org/0000-0002-2544-6979 +oldsnails@hotmail.com + + + +Author + +Tanmuangpak, Kitti +Program of Biology, Department of Science, Faculty of Science and Technology, Loei Rajabhat University, Loei 42000 Thailand + +text + + +ZooKeys + + +2020 + +980 + + +23 +42 + + + + +http://dx.doi.org/10.3897/zookeys.980.54100 + +journal article +http://dx.doi.org/10.3897/zookeys.980.54100 +1313-2970-980-23 +78EED563089C4804A91087DAF1B3D2EB +FD77063CAE3F5DDFA5D3A7714A674E83 + + + + +Aulacospira khaobote Dumrongrojwattana & Panha, 2006 +Figure 2B + + + + +Aulacospria khaobote +Dumrongrojwattana and Panha 2006 +: 122-123, fig. 3. + + + +Type locality. + +Thailand, Wat Tam Khao Bote, an isolated limestone hill of Rayong Province; +13°09'19"N +, +101°38'05"E +. + + + +Types examined. + + +Holotype +. + +ZRCBUU 0083 (BuUZM-MS 0083) (Fig. +2G +). + +Paratype +. + +ZRCBUU 0084 (BuUZM-MS 0084). + + + +Measurements. +H = 1.59-1.89 mm, W = 1.91-2.38 mm. + + +Diagnosis. +Shell minute, triangular; spire high; brownish. Protoconch smooth; teleoconch smooth; body whorl with broad sulcus; tuba very short; peristome not expanded; aperture lacking teeth. + + +Radula. +Unknown. + + +Genital system. +Unknown. + + +Distribution. + +This species is known only from the type locality (Fig. +1 +). + + + + \ No newline at end of file diff --git a/data/38/6B/87/386B87A3A770BE31FF5BF918446522D4.xml b/data/38/6B/87/386B87A3A770BE31FF5BF918446522D4.xml new file mode 100644 index 00000000000..54a21b4bb99 --- /dev/null +++ b/data/38/6B/87/386B87A3A770BE31FF5BF918446522D4.xml @@ -0,0 +1,345 @@ + + + +Further notes on the flower chafer genus Platysodes Westwood, 1873 (Coleoptera Scarabaeidae: Cetoniinae) with description of a new species from Himalaya + + + +Author + +Qiu, Jian-Yue + + + +Author + +Xu, Hao + +text + + +Zootaxa + + +2020 + +2020-12-02 + + +4890 + + +2 + + +192 +200 + + + +journal article +9388 +10.11646/zootaxa.4890.2.2 +e31270aa-00c1-49fc-b98b-d09a9d6ae35e +1175-5326 +4301815 +9DA55ABC-BF33-4A6B-8B1D-3FE21659049A + + + + + + + +Platysodes verlorenii +Westwood, 1873 + + + + + + + +( +Figs. 18–23 +, +27–28 +) + + + + + + +Platysodes jansoni + +(nec Arrow): + +Sakai 2001: 1 + +(Kumpuan, +Thailand +), plate B, fig. +1 ♀ +; + + +Qiu +et al. +2015: 555 + + +(part). + + + + + +New material examined ( +2♁♁, +4♀♀ +). + + +INDONESIA +: + +1♁ ( +NHMB +, Frey Collection), +Java +// +Sammlung Schürhoff +// +Platysodes verloreni + +; + +1♀ +( +MNHN +, +Coll. Lisle +), +Java +, +Mts Kawie +, +J.B.Ledru +1898 + +; + +1♁ ( +CKSJ +), +Mt. Argopuro +, +East Java +, +Indonesia +, + +X. 2015 + +// +Platysodes verloreni Westw., 1873 +, det. +Sakai + +, 2016; + + +MALAYSIA +: + +1♀ +( +BMNH +), +Mt. Kinabalu +, +Brit. N. Borneo, B.M. +1931-386. // +B. N. +BORNEO., +Mt. Kinabalu +, +Kiau +, + +3,000 ft. + +, 1929 // +Platy-sodes + +verloreni +Westw., Determined + +from description. G.J.A + +.; + +1♀ +( +CKSJ +), +Mt. Goram +, + +900 m + +, + +15 km +SW Kapit + +, +Sarawak +, +Borneo +, E. +Malaysia +, + +V.1997 + +, +Tay Poo Min +leg. // +Platysodes verloreni Westw., 1874 +, det. +Sakai + +, 2013; + + +THAILAND + +: +1 ♀ +( +CKSJ +), +Kumpuan +, +Mt. Muan Chone +, +Ranong + +. + + + + +FIGURE 28. +Known distribution of + +Platysodes +Westwood, 1873 + +species (inset photograph shows the dead specimen of +P. ma- doni +Bourgoin, 1923 found at Mount Fanjingshan, Guizhou, China, provided by Ka-Chen Ou-Yang). Distribution data take from + +Qiu +et al. +(2015) + +and specimens examined in the present work. + + + + +Distribution. +Indonesia +; +Malaysia +; +Thailand +( +new record +). More information on distribution can be found in + +Qiu +et al. +(2015) + +. + + + + +Remarks. +The white tomentose maculae on the elytron of + +Platysodes verlorenii + +are fairly varying in number and size ( +Figs. 18–22 +). Apart from the specimens bearing two or three maculae on elytron mentioned in + +Qiu +et al. +(2015) + +, elytron with a single macula also can be observed in a few individuals ( +Fig. 18 +), even the maculae are entirely absent ( +Fig. 19 +). Our re-examination confirmed that the totally black female of + +P. verlorenii + +from southern +Thailand +has been misidentified as + +P. jansoni + +by +Sakai (2001) +and + +Qiu +et al. +(2015) + +since their appearances are rather similar. Moreover, + +Qiu +et al. +(2015) + +noticed the presence of matt area in the elytral distal declivity of +P. ver-lorenii +( +Figs. 22–23 +); nevertheless, they suspected that this species is conspecific to + +P. jansoni + +and + +P. formosanus + +. The examination of further materials shows this character is stable for + +P. verlorenii + +which lets it distinctly different from the latter two. Conversely, this species resembles + +P. sabatinellii + + +new species + +in elytron with white maculae and matt distal declivity ( +Figs. 3 +, +22 +). By the number of grooves on elytron, they can be readily differentiated. + + + + \ No newline at end of file diff --git a/data/38/6B/87/386B87A3A770BE3FFF5BFBFC429C250B.xml b/data/38/6B/87/386B87A3A770BE3FFF5BFBFC429C250B.xml new file mode 100644 index 00000000000..9a5c6d7e542 --- /dev/null +++ b/data/38/6B/87/386B87A3A770BE3FFF5BFBFC429C250B.xml @@ -0,0 +1,230 @@ + + + +Further notes on the flower chafer genus Platysodes Westwood, 1873 (Coleoptera Scarabaeidae: Cetoniinae) with description of a new species from Himalaya + + + +Author + +Qiu, Jian-Yue + + + +Author + +Xu, Hao + +text + + +Zootaxa + + +2020 + +2020-12-02 + + +4890 + + +2 + + +192 +200 + + + +journal article +9388 +10.11646/zootaxa.4890.2.2 +e31270aa-00c1-49fc-b98b-d09a9d6ae35e +1175-5326 +4301815 +9DA55ABC-BF33-4A6B-8B1D-3FE21659049A + + + + + + + +Platysodes madoni +Bourgoin, 1923 + + + + + + + +( +Fig. 28 +) + + + + +New material examined ( +3♁♁, +6♀♀ + +). +VIETNAM +: + + +1♀ +( +BMNH +), +Hoa-Binh +( +Tonkin +), ( +A. de Cooman +), +Coll. J. Clermont + +// Bourgoin Coll. B. M. 1938-252; + +1♀ +( +MNHN +), +Tonkin +// + +Platysodes madoni +Bourg., R.Paulian + +det.; 1 + +♁, + +1♀ +( +MNHN +), +TONKIN +, +Lac Thô +, +HOA BINH +, A.DE COOMAN // +MUSÉUM PARIS +, 1931, A. de COOMAN; 1 + +♁, + +1♀ +( +MNHN +), +Tonkin +occ., +Rég. De +Hoa Binh +, +R.P.A. de Cooman +, 1918; + + +1♁ ( +MNHN +), +Tuyen-Quang +, ( +Tonkin +) +Rau +// +MUSÉUM PARIS +, ( +Coll. Ph. Francois +), +Coll. L. Bedel + +1922; + +1♀ +( +MNHN +), HUE +Annam +// +MUSÉUM PARIS +, +E. Lemoult +, 1918 // + +Platysodes madoni +Bourg., R.Paulian + +det + +.; + +1♀ +( +MNHN +), +Tuyen-Quang +// +MUSÉUM PARIS +, 1958, +Coll. M. Pic. + + + + + +Distribution. +China +: +Guangdong +, +Guizhou +, +Guangxi +, +Yunnan +; +Vietnam +; +Laos +; +Malaysia +. More information on distribution can be found in + +Qiu +et al. +(2015) + +. + + + + +Remarks. +On +6th February 2019 +, an incomplete remain of + +Platysodes madoni + +was found at Panxi of the Mount Fanjingshan, northeastern +Guizhou +, +China +(Kai-Chen Ou-Yang, personal communication, +August 2020 +). This record extends the distributional range of this species northward ( +Fig. 28 +). + + + + \ No newline at end of file diff --git a/data/38/6B/87/386B87A3A775BE3AFF5BFD45420A26B8.xml b/data/38/6B/87/386B87A3A775BE3AFF5BFD45420A26B8.xml new file mode 100644 index 00000000000..620058ae213 --- /dev/null +++ b/data/38/6B/87/386B87A3A775BE3AFF5BFD45420A26B8.xml @@ -0,0 +1,246 @@ + + + +Further notes on the flower chafer genus Platysodes Westwood, 1873 (Coleoptera Scarabaeidae: Cetoniinae) with description of a new species from Himalaya + + + +Author + +Qiu, Jian-Yue + + + +Author + +Xu, Hao + +text + + +Zootaxa + + +2020 + +2020-12-02 + + +4890 + + +2 + + +192 +200 + + + +journal article +9388 +10.11646/zootaxa.4890.2.2 +e31270aa-00c1-49fc-b98b-d09a9d6ae35e +1175-5326 +4301815 +9DA55ABC-BF33-4A6B-8B1D-3FE21659049A + + + + + + + +Platysodes formosanus +Kobayashi, 1990 + + + + + + + +( +Figs. 9–12 +, +25 +, +28 +) + + + + +New material examined ( +1♁, +2♀♀ +). + + +CHINA +: +Guangdong +: + +1♀ +( +MYNU +), + +2011.V.18 + +, +Longyangdong Park +, Guang-zhou, +Ling-Ting Chen +leg. + + + +Taiwan +: + +1♀ +( +CKSJ +), +Fushan +, +Taipei +Hsien +, + +2000.VII.11 + +, +H. Sugaya +leg. // + +Platysodes formosanus +H. +Kobayashi, 1990 + +, det. +K. Sakai + +, + +2013; 1♁ ( +CKSJ +), + +2008.XI.7 + +, +Shihtyutou +, +Nantou +, +C. C. Lo +leg. // + +Platysodes formosanus +H. Kobayashi, 1989 + +, det. +K. Sakai + +, 2013. + + + + +Distribution. +China +: +Guangdong +( +new record +), +Taiwan +. + + + + +Remarks. + +Platysodes formosanus + +is extremely similar to + +P. jansoni + +and the parameres of both also show no differences ( +Figs. 12, 17 +), and that resulted in + +Qiu +et al. +(2015) + +presumed them as the same species. Traditionally, the former is characterized by elytron bearing one tomentose macula and restricted to +Taiwan Island +( +Kobayashi 1990 +; + +Qiu +et al. +2015 + +), while the latter is totally black and distributed in eastern +India +and Indochina ( +Arrow 1910 +; + +Qiu +et al. +2015 + +). However, we recently obtained a female whose appearance perfectly matches the characteristics of + +P. formosanus + +( +Fig. 9 +), but it originated from Guangzhou ( +Guangdong +, +China +) where located on the southeastern edge of the Asian continent and between the Indochinese Peninsula and +Taiwan Island +( +Fig. 28 +). Furthermore, an individual of + +P. formosanus + +bearing an indistinct macula on elytron (nearly disappeared) was found from +Taiwan +( +Fig. 25 +), and a female of + +P. jansoni + +with two maculae was discovered from +Vietnam +( +Fig. 13 +). The two specimens have here verified the prediction proposed by + +Qiu +et al. +(2015) + +that the variability of tomentose maculae on elytron can be observed in a species of wide distribution. Therefore, neither endemism of + +P. formosanus + +nor morphological differences between the two species are well established, but we would like to formally propose the synonymy when sufficient material got rather than synonymize them at present. + + + + \ No newline at end of file diff --git a/data/38/6B/87/386B87A3A775BE3DFF5BF98942B923A7.xml b/data/38/6B/87/386B87A3A775BE3DFF5BF98942B923A7.xml new file mode 100644 index 00000000000..06a8f558201 --- /dev/null +++ b/data/38/6B/87/386B87A3A775BE3DFF5BF98942B923A7.xml @@ -0,0 +1,164 @@ + + + +Further notes on the flower chafer genus Platysodes Westwood, 1873 (Coleoptera Scarabaeidae: Cetoniinae) with description of a new species from Himalaya + + + +Author + +Qiu, Jian-Yue + + + +Author + +Xu, Hao + +text + + +Zootaxa + + +2020 + +2020-12-02 + + +4890 + + +2 + + +192 +200 + + + +journal article +9388 +10.11646/zootaxa.4890.2.2 +e31270aa-00c1-49fc-b98b-d09a9d6ae35e +1175-5326 +4301815 +9DA55ABC-BF33-4A6B-8B1D-3FE21659049A + + + + + + + +Platysodes jansoni +Arrow, 1910 + + + + + + + +( +Figs. 13–17 +, +26 +, +28 +) + + + + +New material examined ( +1♁, +1♀ +). + + +VIETNAM +: + +1♁ ( +MNHN +), +Hoa-Binh +( +Tonkin +), ( +A. de Cooman +), +Coll. J. +Cler-mont// +Platysodes +atronitens m. n.sp., + + +HOLOTYPE +♁, G.RUTER dét.1977 // +Platysodes jansoni Arrow, Compare +type par +Krikken +(Mus. Leiden), G.RUTER dét. 1978; +1♀ +( +BPBM +), + + +VIET NAM. +M’Drak, E. +of +Ban Me Thuot +, + +4-600 m + +, 8-19.XII.[19]60 // +C.M. Yoshimoto +, Collector // + +// +ALLOTYPE +// Javrigiella atronitens m. n.sp., ALLO-TYPE + +, G.RUTER dét.1976 // +Platysodes +atronitens m. n.sp., +ALLOTYPE + +, G.RUTER dét.1977 // +Platysodes jansoni Arrow, G.RUTER +dét. 1979 + +. + + + + +Distribution. +India +; +Vietnam +. + + + + +Remarks. +The label data of the two newly examined specimens revealed their identity has been constantly changed by the late Gaston Ruter (1898–1979). Ruter initially plan to introduce a new genus for them in 1976, and he later realized the two belonging to the genus + +Platysodes + +. According to the letter he sent to Gordon M. Nishida (former collections manager of BPBM) in 1979, he finally identified them as + +P. jansoni + +with the help from the museum in Leiden (James H. Boone, personal communication, +October 2016 +). + + + + \ No newline at end of file diff --git a/data/38/6B/87/386B87A3A777BE3AFF5BFDF940B721F4.xml b/data/38/6B/87/386B87A3A777BE3AFF5BFDF940B721F4.xml new file mode 100644 index 00000000000..7cf2c8a50e3 --- /dev/null +++ b/data/38/6B/87/386B87A3A777BE3AFF5BFDF940B721F4.xml @@ -0,0 +1,351 @@ + + + +Further notes on the flower chafer genus Platysodes Westwood, 1873 (Coleoptera Scarabaeidae: Cetoniinae) with description of a new species from Himalaya + + + +Author + +Qiu, Jian-Yue + + + +Author + +Xu, Hao + +text + + +Zootaxa + + +2020 + +2020-12-02 + + +4890 + + +2 + + +192 +200 + + + +journal article +9388 +10.11646/zootaxa.4890.2.2 +e31270aa-00c1-49fc-b98b-d09a9d6ae35e +1175-5326 +4301815 +9DA55ABC-BF33-4A6B-8B1D-3FE21659049A + + + + + + + +Platysodes sabatinellii +Qiu & Xu + +, +new species + + + + + + +( +Figs. 1–8 +, +24 +, +28 +) + + + +Platysodes jansoni + +(nec Arrow): Sabatinelli 1984: 163 (Darjeeling, +India +), fig. 3 parameres. + + + + +Type material. +The +holotype +of + +Platysodes sabatinellii + + +new species + +in BMNH was left undissected, and the male genitalia illustrated in the plate belongs to the + +paratype +from +Darjeeling +( +Figs. 4–5 +) + +. + + +Holotype + +(♁, +Figs. 1–3 +, +BMNH +): UPPER +BURMA +: +Nam Tamai Valley +, + +29.vii.1938 + +, +R. Kaulback. +, B.M. 1938-741// +Alt. + +3,000 ft. + +, +Lat. N. +27°42′, +Long. +E.97°54 + +′; + + +Paratypes + +(2♁♁, +1♀ +): + +MYANMAR +: + +1♁ ( +Fig. 6 +, +CKSJ +), 2001.VII, near +Putao, N. +Kachin, +Myanmar +; + + + +INDIA +: + +1♀ +( + +allotype + +, +Fig. 7 +, +MNHN +, +Coll. De +Lisle), +Sikkim +, +März +, +April, H +. Fruhstorfer // +Platysodes jansoni Arrow, M. O. de Lisle +det. 1968; + + +1♁ ( +NHMB +), +Darjeeling Distr. +, +India Bhakta B. +// +Sakyong +, + +1140 m + +, 25.IX.[19]81 + +. + + + +Holotype +(male). General: + +Body elongate oval, black, glabrous, sparsely microsculptured. +Head: +Dorsal surface arciform; sides of with sparse, tiny and shallow punctures. Clypeus short, arc-shaped, anterior margin raised. Eye canthus extending laterally, narrow, long. Antenna simple and antennal club dark brown. +Mentum +expanding, strongly extended basally; with sparse, semicircular punctures. +Pronotum: +Suboctagonal, flat and smooth; with few small, elliptical punctures near anterior angle. Anterior margin straight, posterior margin notched in front of scutellum. +Scutellum: +Long triangular; median area glabrous; basal area with few striolae, sides with few punctures. +Elytron: +Sutural costa wide. Two grooves on disc; longer groove deep, with large, U-shaped punctures, punctures partly combined near discolateral costa; shorter groove shallow and narrow, with few large, U-shaped punctures. Other area of elytral surface with sparse, small, U-shaped or round punctures. Two irregularly shaped, white tomentous maculae: one near middle of sutural costa and the other in longer groove. Distal declivity matt, sparsely punctured. Apicosutural angle obtuse, not pointed. +Mesepimeron and metepisternum: +Surface with arcuate punctures and sinuous striolae. +Metepimeron: +Surface with few tiny, round punctures. +Sternum: +Preprosternum with long, brown setae along anterior margin; preprosternal apophysis slightly raised. Postprosternum glabrous, with-out punctures. Mesosternum with dense, arcuate punctures and sinuous striolae. Disc of metasternum glabrous, without punctures; sides with large, arcuate punctures and sinuous striolae. +Pygidium: +Surface clad with sparse, small, arcuate punctures. Shape almost semicircular and midline slightly raised in dorsal view. Apex strongly and transversely ridged in lateral view. +Abdomen: +Seven sternites, six sternites visible. Median portion of abdominal sternites slightly depressed, glabrous; sides with sparse, large U or C-shaped punctures. Last spiracle prominent, rounded. +Legs: +Mesocoxa strongly approximate. Outer margin of trochanters with short, compact, brown setae. Profemur covered with dense short, sinuous striolae. Femora and tibiae covered with dense sinuous striolae, and elliptical and arcuate setiferous punctures; setae short. Tibiae short, a small white tomentous patch at the base of each tibia. Protibia bidentate, spur acute. Mesotibia and metatibia with a strong external protrusion, two sharp teeth on apex. Tarsi slender, short. +Parameres: +Falcate in lateral view. In apical view, distal half part of each paramere expanded and divided into two lobes; distal lobes slender, close to each other; basal lobes wide, overlapped each other, apex protruding like barb ( +Figs. 4–5 +). + + + +Paratypes +. + +All the three +paratypes +have a small white tomentous macula behind anteapical umbone of elytron. Each of abdominal sternite II to V with a pair of small white, tomentous patches on both sides in the female +paratype +. Female is extremely similar to male and only can be distinguished by its abdomen not depressed medially. + + + + +FIGURES 1–8. +Type specimens of + +Platysodes sabatinellii +Qiu & Xu + +, + +new species + +. 1–3, holotype (BMNH): 1, dorsal view; 2, ventral view; 3, oblique view. 4–5, parameres of paratype in lateral and apical view (Darjeeling, NHMB; provided by Guido Sabatinelli). 6, paratype (CKSJ). 7–8, allotype (MNHN): 7, dorsal view; 8, distal declivity of elytra. Red arrows emphasize the matt area. + + + + +Measurements. +Body length 23.1–25.0 mm ( +holotype +23.5 mm), width 9.1–10.9 mm ( +holotype +9.7 mm). + + + + +Differential diagnosis. +The new species can be separated from all other + +Platysodes + +species by the two longitudinal grooves on the elytral disc. + + + + +Etymology. +The new species is named in honor of Dr. Guido Sabatinelli, an Italian taxonomist of scarabs who found this species for the first time. + + + + +Distribution. +India +; +Myanmar +. + + + + +Remarks. + +Platysodes sabatinellii + + +new species + +is quite different from + +P. jansoni + +in elytron. Elytron of the latter is smooth and without groove ( +Fig. 26 +), but that of the new species is matt in the distal declivity ( +Fig. 3 +) and with two grooves in the disc ( +Fig. 24 +). Besides, the basal lobes of their parameres are different in shape, the apex of + +P. sabatinellii + + +new species + +is produced ( +Fig.5 +), whereas that of the latter is blunt ( +Fig. 17 +). Specimen of +P. sabatinel-lii +new species +was firstly reported by Sabatinelli (1984) from Darjeeling, North +India +. It was misidentified as + +P. jansoni + +although he already pointed out that the distal declivity of elytron is matt. He subjectively thought that this feature was overlooked by +Arrow (1910) +. According to the current distributional map ( +Fig. 28 +), + +P. sabatinellii + + +new species + +probably occurs along the south side of the Himalayas, including the vast multi-altitudes primary forests in southeastern +Xizang +of +China +. + + + + \ No newline at end of file diff --git a/data/38/6B/87/386B87A3A77EBE31FF5BFE6444C1207D.xml b/data/38/6B/87/386B87A3A77EBE31FF5BFE6444C1207D.xml new file mode 100644 index 00000000000..17b64f4bf91 --- /dev/null +++ b/data/38/6B/87/386B87A3A77EBE31FF5BFE6444C1207D.xml @@ -0,0 +1,159 @@ + + + +Further notes on the flower chafer genus Platysodes Westwood, 1873 (Coleoptera Scarabaeidae: Cetoniinae) with description of a new species from Himalaya + + + +Author + +Qiu, Jian-Yue + + + +Author + +Xu, Hao + +text + + +Zootaxa + + +2020 + +2020-12-02 + + +4890 + + +2 + + +192 +200 + + + +journal article +9388 +10.11646/zootaxa.4890.2.2 +e31270aa-00c1-49fc-b98b-d09a9d6ae35e +1175-5326 +4301815 +9DA55ABC-BF33-4A6B-8B1D-3FE21659049A + + + + + + +Key to the species of the genus + +Platysodes + +(modified from + +Qiu +et al. +2015 + +) + + + + + + + + +1. Punctures on disc of pronotum dense and distinct; last spiracle distinctly protruding............ + +P. madoni +Bourgoin, 1923 + + + + +- Punctures on disc of pronotum sparse and indistinct; last spiracle prominent....................................... 2 + + + + + +2. Distal declivity of elytron smooth ( +Figs. 11, 16 +)............................................................. 3 + + + + +- Distal declivity of elytron matt ( +Figs. 3 +, +23 +)................................................................ 4 + + + + + + +3. Elytron usually completely black, without white maculae ( +Figs. 14–15 +, +26 +); distributed in Indochina.. + +P. jansoni +Arrow, 1910 + + + + + +- Elytron with one white maculae ( +Figs. 9–10 +); distributed in southern +China +mainland and +Taiwan Island +............................................................................................ + +P. formosanus +Kobayashi, 1990 + + + + + + + +4. Elytron with one groove ( +Fig. 27 +)................................................. + +P. verlorenii +Westwood, 1873 + + + + + +- Elytron with two grooves ( +Fig. 24 +)................................................... + +P. sabatinellii + + +new species + + + + + + + \ No newline at end of file diff --git a/data/38/6B/B7/386BB745FBFB24B4E486F0909DDD7DC9.xml b/data/38/6B/B7/386BB745FBFB24B4E486F0909DDD7DC9.xml new file mode 100644 index 00000000000..3e92407533d --- /dev/null +++ b/data/38/6B/B7/386BB745FBFB24B4E486F0909DDD7DC9.xml @@ -0,0 +1,52 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Chimaera +[ +gen. nov. +] + + + + +Spiracula +solitaria sub collo. + + +Oris +labium superius bipartitum. + + +Dentes +primores incisores, bini supra infraque. + + + + \ No newline at end of file diff --git a/data/38/6C/0C/386C0C393DEE55D18EEEF40462B9C4FE.xml b/data/38/6C/0C/386C0C393DEE55D18EEEF40462B9C4FE.xml new file mode 100644 index 00000000000..0a06dec4020 --- /dev/null +++ b/data/38/6C/0C/386C0C393DEE55D18EEEF40462B9C4FE.xml @@ -0,0 +1,252 @@ + + + +The concluding chapter: recircumscription of Goodenia (Goodeniaceae) to include four allied genera with an updated infrageneric classification + + + +Author + +Shepherd, Kelly A. +Western Australian Herbarium, Department of Biodiversity, Conservation & Attractions, Kensington, WA 6151, Australia +https://orcid.org/0000-0003-1627-7891 +kelly.shepherd@dbca.wa.gov.au + + + +Author + +Lepschi, Brendan J. +Australian National Herbarium, Centre for Australian National Biodiversity Research, GPO Box 1700, Canberra, ACT, 2601, Australia + + + +Author + +Johnson, Eden A. +Department of Biology, University of Mississippi, Oxford, MS 38677, USA + + + +Author + +Gardner, Andrew G. +Department of Biological Sciences, California State University, Stanislaus, Turlock, CA 95382, USA + + + +Author + +Sessa, Emily B. +Department of Biology, University of Florida, Gainesville, FL 32607, USA + + + +Author + +Jabaily, Rachel S. +Department of Organismal Biology & Ecology, Colorado College, Colorado Springs, CO 80903, USA + +text + + +PhytoKeys + + +2020 + +152 + + +27 +104 + + + + +http://dx.doi.org/10.3897/phytokeys.152.49604 + +journal article +http://dx.doi.org/10.3897/phytokeys.152.49604 +1314-2003-152-27 +9E670F26B4635D2FA9E36777E3C2DD70 + + + + +Goodenia subg. Goodenia sect. Rosulatae (K.Krause) K.A.Sheph., comb. et +stat. nov. + + + + += +Goodenia ser. Rosulatae +K.Krause in H.G.A.Engler (ed.), Pflanzenr. 54: 46, 52. 1912 - Type (designated by Carolin in George (ed.), Fl. Australia 35: 331. 1992): +G. geniculata +R.Br. + + += +Catospermum +Benth., +Hooker's +Icon. Pl. 11: t. 1028. 1867 - Type: +C. muelleri +Benth., +nom. illeg +. ≡ +Goodenia goodeniacea +(F.Muell.) Carolin. + + + +Description. + +Herbs +or occasionally +subshrubs +, usually with multicellular hairs sometimes becoming glabrescent, or rarely with simple and glandular hairs. +Leaves +basal and/or cauline. +Flowers +usually in racemes or solitary in leaf axils; pedicels usually not articulate. +Corolla +bilabiate. + + + +Number of taxa and distribution. +This section includes 28 species found in every state of Australia across a range of biomes with some species extending into arid central inland regions. + + +Included species. + + +G. affinis + +de Vriese, + +G. arenicola + +Carolin, + +G. atriplexifolia + +A.E.Holland & T.P. Boyle, + +G. blackiana + +Carolin, + +G. centralis + +Carolin, + +G. convexa + +Carolin, + +G. delicata + +Carolin, + +G. disperma + +Mueller, + +G. dyeri + +K.Krause, + +G. expansa + +A.E.Holland & T.P.Boyle, + +G. fordiana + +Carolin, + +G. geniculata + +R.Br., + +G. glabra + +R.Br., + +G. goodeniacea + +(F.Muell.) Carolin, + +G. hederacea + +Sm., +G. hederacea subsp. alpestris +(K.Krause) Carolin, +G. hederacea Sm. subsp. hederacea +, + +G. heterophylla + +Sm., +G. heterophylla subsp. eglandulosa +Carolin, +G. heterophylla Sm. subsp. heterophylla +, +G. heterophylla subsp. montana +Carolin, +G. heterophylla subsp. teucriifolia +(F.Muell.) Carolin, + +G. lanata + +R.Br., + +G. mueckeana + +F.Muell., + +G. peacockiana + +Carolin, + +G. robusta + +(Benth.) K.Krause, + +G. rotundifolia + +R.Br., + +G. rupestris + +Carolin, + +G. schwerinensis + +Carolin, + +G. stephensonii + +F.Muell., + +G. tripartita + +Carolin, + +G. viridula + +Carolin, + +G. willisiana + +Carolin, + +G. xanthosperma + +F.Muell. + + + + \ No newline at end of file diff --git a/data/38/6C/96/386C966F772A9F01FDDE4578B19BC20B.xml b/data/38/6C/96/386C966F772A9F01FDDE4578B19BC20B.xml new file mode 100644 index 00000000000..7be9790da9a --- /dev/null +++ b/data/38/6C/96/386C966F772A9F01FDDE4578B19BC20B.xml @@ -0,0 +1,231 @@ + + + +Two new troglobitic species of the genus Telema (Araneae, Telemidae) from Guizhou, southwestern China + + + +Author + +Chen, Hui-Ming + + + +Author + +Zhu, Ming-Sheng + +text + + +Journal of Natural History + + +2009 + +2009-06-16 + + +43 + + +27 - 28 + + +1705 +1713 + + + + +http://dx.doi.org/10.1080/00222930902968791 + +journal article +10.1080/00222930902968791 +1464-5262 +5216621 + + + + + + +Telema feilong + +sp. nov. + + + + + +( +Figure 2A–K +) + + +Material + + + + +Holotype +male. + +Found in Feilong Cave +(24°55¢ N, 104°53¢ E, + +1335 m +above sea level + +), +Shangjiao village +, +Jingnan town +, +Xingyi +city, +Guizhou province +, + +25 May 2004 + +, collected by +H.M. Chen +and +Y.Q. Zhang +( +MLR +). + + + + + +Paratypes +. + +Three males and +one female +, same data as holotype ( +MHBU +) + +. + + +Diagnosis + + +The new species is similar to + +T. dongbei + +, + +T. spina + +. Male + +T. feilong + +can be distinguished from other + +Telema +species + +by different shapes of bulb ( +Figure 2C,D +); from + +T. dongbei + +by short triangular bulbal apophysis (tapering in + +T. dongbei + +), the> 90° angle of bulbal apophysis to the bulb (<90° in + +T. dongbei + +); from + +T. spina + +by absence of eyes, absence of strong spines in palpal tarsus. Females can be distinguished by different shapes of their spermathecal tubes ( +Figure 2J +). + + +Description + + + +Male +holotype +. + +Total length 1.65. Cephalothorax 0.73 long, 0.60 wide, 0.35 high; yellowish, no fovea, with two pairs of short setae ( +Figure 2B +). Eyeless. Chelicerae 0.425 long, yellowish; fangs long, slender; promargin of chelicerae furrowed with two denticles (near base of fang), three denticulates, retromargin with four barely visible granulous denticulates (one next to base of fang, +Figure 2G +). Sternum 0.48 long, 0.38 wide, yellowish, smooth with a few bristles. Labium 0.075 long, 0.175 wide. Total length of palpus 1.23 (sum of femur, patella, tibia and tarsus); palpal coxae 0.25 long, 0.18 wide, the outer side bends inwards forming a angled apex ( +Figure 2E +); femur 0.32 long; patella 0.14 long; tibia 0.26 long; tarsus 0.50 long, in dorsal view broad at base but narrow at intermediate section and distal end, with well-developed, prolateral cymbial apophysis, distal end of the apophysis bears long bristles ( +Figure 2C,F +); bulb 0.55 long, oval, simple, with a short triangular apophysis that is slightly downwardly warped at distal end ( +Figure 2C,D +), slightly longer than tarsus. Colulus rhomboidal in shape ( +Figure 2H +), 0.12 long, 0.13 wide. Abdomen smoothly ovoid, 0.88 long, 0.70 wide, greyish, with sparsely short hairs around the margin. Gonopore on shallow elevation, surrounded by a tuft of hairs. Legs yellowish, with a long spine on patella II, tibia (I, II, IV), femur IV; femur I, femur IV slightly curved in dorsal view; leg formula: 1243. Leg measurements: leg I 6.05 (1.78, 0.20, 1.93, 1.35, 0.80), leg II 5.35 (1.65, 0.23, 1.65, 1.18, 0.65), leg III 3.88 (1.20, 0.23, 1.13, 0.78, 0.55), leg IV 4.55 (1.60, 0.20, 1.10, 1.00, 0.65). + + + +Female +paratype +. + +Specimen from same locality as +holotype +. It is similar in overall appearance to male, but slightly larger. Total length 1.75. Cephalothorax 0.75 long, 0.58 wide, 0.40 high; yellowish, no fovea. Eyeless. Chelicerae 0.38 long, yellowish; fangs long, slender; number, position of denticles and denticulates for chelicerae furrow same with male. Sternum 0.45 long, 0.38 wide, yellowish, shape same as male. Labium 0.075 long, 0.175 wide. Total length of palpus 0.83 (the sum of femur, patella, tibia and tarsus,); palpal coxae 0.25 long, 0.15 wide; femur 0.25 long; patella 0.10 long; tibia 0.18 long; tarsus 0.30 long. Colulus rhomboidal in shape ( +Figure 2K +), 0.10 long, 0.10 wide. Abdomen smoothly ovoid, 1.00 long, 0.88 wide, greyish. Epigynum with one row of hairs on epigynal plate, another row posterior epigastric furrow ( +Figure 2I +); spermatheca narrow, long, curved posteriorly, obtuse at apex, triangular at base ( +Figure 2J +). Legs yellowish, with one long spine on patella and tibia of every leg; femur I, femur IV slightly curved in dorsal view; leg formula: 1243. Leg measurements: leg I 5.90 (1.85, 0.23, 1.78, 1.28, 0.78), leg II 5.30 (1.63, 0.25, 1.55, 1.15, 0.73), leg III 3.88 (1.33, 0.20, 1.08, 0.75, 0.53), leg IV 4.80 (1.60, 0.25, 1.33, 1.00, 0.63). + + + +Figure 2. + +Telema feilong + +sp. nov. +, male holotype and female paratype: (A) male body, lateral view; (B) male body, dorsal view; (C) male left palp, prolateral view; (D) male left palp, retrolateral view; (E) male palpal coxae, labium and sternum in ventral view; (F) male palpal cymbium in dorsal view; (G) male left chelicerae ventral view; (H) male colulus; (I) female genitalia ventral view; (J) female genitalia dorsal view; (K) female colulus. Scale bars: A, B, 0.2 mm; C–K, 0.1 mm. + + + +Distribution + + +The species is known only from the +type +locality ( +Figure 1 +). + + +Etymology + + +The specific name refers to the +type +locality. + + +Level of cave adaptation + +This species lives entirely in the dark parts of the cave and has no functioning eyes and no pigmentation. + + + \ No newline at end of file diff --git a/data/38/6C/96/386C966F772C9F0CFDC44708B3A7C01B.xml b/data/38/6C/96/386C966F772C9F0CFDC44708B3A7C01B.xml new file mode 100644 index 00000000000..a1a9d61d10e --- /dev/null +++ b/data/38/6C/96/386C966F772C9F0CFDC44708B3A7C01B.xml @@ -0,0 +1,345 @@ + + + +Two new troglobitic species of the genus Telema (Araneae, Telemidae) from Guizhou, southwestern China + + + +Author + +Chen, Hui-Ming + + + +Author + +Zhu, Ming-Sheng + +text + + +Journal of Natural History + + +2009 + +2009-06-16 + + +43 + + +27 - 28 + + +1705 +1713 + + + + +http://dx.doi.org/10.1080/00222930902968791 + +journal article +10.1080/00222930902968791 +1464-5262 +5216621 + + + + + + +Telema zhewang + +sp. nov. + + + + + +( +Figure 3A–D,F–L,O,P +) + + +Material + + + + +Holotype +male. + +Collected from +Zhoujia Cave +(25°11¢ N, 105°55¢ E, + +600 m +above sea level + +), +Zhewang village +, +Qingping town +, +Ceheng county +, +Guizhou province +, + +23 May 2004 + +, collected by +H.M. Chen +and +Y.Q. Zhang +( +MLR +). + + + + + +Paratype +. + +Thirteen males and +22 females +, same data as holotype ( +MHBU +) + +. + + + +Other comparative material. +Telema liangxi + +, + +four males +and +nine females +from +Jinshi Cave +(25°17¢28.96¢¢ N, 108°03¢52.58¢¢ E, + +534 m +above sea level + +), only +4 km +from the location of the +holotype +, +Liangxi Cave +, + +9 October 2001 + +, collected by +H.M. Chen. + + + +Diagnosis + + +The new species is similar to + +T. liangxi + +but can be distinguished by the strongly reduced prolateral cymbial apophysis (well developed in + +T. liangxi + +, +Figure 3E.F +) in male, spermathecae coiled more than one circuit in lateral view (less than one circuit in + +T. liangxi + +, +Figure 3J–N +) in female. + + +Description + + + +Male +holotype +. + +Total length 1.30. Cephalothorax 0.63 long, 0.58 wide, 0.39 high; yellowish, no fovea, with two pairs of short setae. Eyeless. Chelicerae 0.284 long, yellowish; fangs long, slender; similar to + +T. feilong + +, promargin of chelicerae furrow with two denticles, three denticulates, retromargin with four granulous denticulates. Sternum 0.37 long, 0.28 wide, yellowish, smooth with a few bristles. Labium 0.065 long, 0.14 wide. Total length of palpus 1.17 (sum of femur, patella, tibia tarsus); palpal coxae 0.21 long, 0.13 wide; femur 0.28 long; patella 0.13 long; tibia 0.22 long; tarsus 0.54 long, with a strongly reduced prolateral cymbial apophysis, distal end of the apophysis bears two long bristles ( +Figure 3F +); bulb 0.67 long, roughly globular, simple, with a tube-like apophysis that is slightly oblate ( +Figure 3C,D +), slightly longer than tarsus. Colulus rhomboidal in shape ( +Figure 3G +), 0.09 long, 0.10 wide. Abdomen smoothly ovoid, 0.77 long, 0.66 wide, yellowish, with hairs. Gonopore on shallow elevation. Legs yellowish, with a long spine on tibia of every leg; femur I, femur IV slightly curved in dorsal view; leg formula: 1243. Leg measurements: leg I 5.00 (1.47, 0.18, 1.63, 1.08, 0.65), leg II 4.10 (1.33, 0.18, 1.15, 0.90, 0.55), leg III 3.01 (0.95, 0.18, 0.83, 0.60, 0.48), leg IV 3.43 (0.98, 0.18, 1.08, 0.73, 0.48). + + + +Figure 3. + +Telema zhewang + +sp. nov. +, male holotype, female paratype and + +Telema liangxi + +comparative material: (A) + +T. zhewang + +female body, lateral view; (B) + +T. zhewang + +female body, dorsal view; (C) + +T. zhewang + +male left palp, prolateral view; (D) + +T. zhewang + +male left palp, retrolateral view; (E) + +T. liangxi + +male palpal cymbium in dorsal view; (F) + +T. zhewang + +male palpal cymbium in dorsal view; (G) + +T. zhewang + +male colulus; (H) + +T. zhewang + +female genitalia ventral view; (I) + +T. zhewang + +female genitalia dorsal view; (J–L) + +T. zhewang + +female spermathecae in lateral view; (M, N) + +T. liangxi + +female spermathecae in lateral view; (O) + +T. zhewang + +female palpal coxae, labium and sternum in ventral view; (P) + +T. zhewang + +female left chelicerae ventral view; (Q) + +T. zhewang + +female colulus. Scale bars: A, B, 0.2 mm; C–Q, 0.1 mm. + + + + +Female +paratype +. + +Specimen from same locality as +holotype +. It is similar in overall appearance to male, slightly bigger ( +Figure 3A,B +). Total length 1.38. Cephalothorax 0.55 long, 0.50 wide, 0.35 high; yellowish, no fovea. Eyeless. Chelicerae 0.28 long, yellowish; fangs long, slender; number, position of denticles and denticulates for chelicerae furrow same with male ( +Figure 3P +). Sternum 0.31 long, 0.28 wide, yellowish, shape same as male ( +Figure 3O +). Labium 0.065 long, 0.13 wide. Total length of palpus 0.78 (the sum of femur, patella, tibia and tarsus); palpal coxae 0.21 long, 0.10 wide; femur 0.23 long; patella 0.10 long; tibia 0.15 long; tarsus 0.30 long. Colulus rhomboidal in shape ( +Figure 3Q +), 0.65 long, 0.09 wide. Abdomen smoothly ovoid, 0.83 long, 0.75 wide, yellowish. Epigynum with one row of hairs on epigynal plate, and another row on posterior epigastric furrow ( +Figure 3H +); spermatheca narrow, curved posteriorly, obtuse and swollen at apex ( +Figure 3I +). Legs yellowish, with one long spine on tibia of every leg; femur I, femur IV slightly curved in dorsal view; leg formula: 1243. Leg measurements: leg I 4.80 (1.50, 0.20, 1.50, 0.98, 0.63), leg II 4.13 (1.33, 0.20, 1.25, 0.80, 0.55), leg III 3.78 (1.30, 0.20, 1.28, 0.58, 0.43), leg IV 3.65 (1.23, 0.18, 1.05, 0.70, 0.50). + + +Distribution + + +The species is known only from the +type +locality ( +Figure 1 +). + + +Etymology + + +The specific name refers to the +type +locality. + + +Level of cave adaptation + +This species lives entirely in the dark parts of caves and has no functioning eyes and no pigmentation. + +Natural history + + + +Telema feilong + +, + +T. zhewang + +, + +T. liangxi + +and + +T. dongbei + +are small spiders, generally restricted to moist caves. Spiders were found in complete darkness in the constanttemperature zone with relatively high humidity but without strong wind or air flows around the cave. The web is a woven sheet about +10 cm +in diameter, along the cave base plate and cave sediments, such as clay, silt and gravel. Prey includes dayflies and mosquitoes. Most individual + +T. liangxi + +and + +T. dongbei + +are distributed in the middle layer caves of the cave system in the middle stages, rare individuals were found in the upper layer caves in early stages and in the lower layer caves in late stages. + +Telema feilong + +and + +T. zhewang + +collected from layer caves, but rarely. + + + + \ No newline at end of file diff --git a/data/38/6C/A5/386CA5452FDAF49170148CD90A1F9E27.xml b/data/38/6C/A5/386CA5452FDAF49170148CD90A1F9E27.xml new file mode 100644 index 00000000000..ae2e71f79f6 --- /dev/null +++ b/data/38/6C/A5/386CA5452FDAF49170148CD90A1F9E27.xml @@ -0,0 +1,54 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828-4-9042 + + + + +Gelis pulicarius (Fabricius, 1793) + + + + +Ichneumon pulicarius +Fabricius, 1793 + + +hoffmannseggii +(Gravenhorst, 1815, +Ichneumon +) + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC02A542FF678946FB9CF8AF.xml b/data/38/6C/C6/386CC616DC02A542FF678946FB9CF8AF.xml new file mode 100644 index 00000000000..70a37db0065 --- /dev/null +++ b/data/38/6C/C6/386CC616DC02A542FF678946FB9CF8AF.xml @@ -0,0 +1,649 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Sycettusa hastifera +( +Row, 1909 +) + + + + + +Figs 68a–g +, +69a–f +, +70a–f + + + + + + +Grantilla hastifera + +Row, 1909 +: 200 + + +, pl. 19 figs 3–4, text fig. 3. + + + + +? + +Grantilla quadriradiata + +Row, 1909 +: 198 + + +, pl. 19 fig. 2, text fig. 2. + + + + + +Grantessa hastifera + +; Dendy 1913: 19, pl. 2 fig. 6; + +Dendy 1916 +: 81 + +, pl. 1 fig.2, pl. 2 fig. 7; + +Borojević 1967 +: 210 + +, fig. 17. + + + + + + + +Material +examined. + +RMNH +Por. +9587, +Saudi Arabia +, +Jeddah +, near Thuwal, Abu Gishaa, +22.255194°N +39.025639°E +, depth + +12 m + +, scuba, coll. +N.J. de Voogd +, field nr. THU06/JED082, + +9 November 2014 + + +; + +RMNH +Por. +9644, +Saudi Arabia +, +Jeddah +, near Thuwal, Um Alsawi, +22.239306°N +38.985139°E +, scuba, coll. +N.J. de Voogd +, field nr. THU08/JED144, + +11 November 2014 + + +; + +RMNH +Por. +9645, +Saudi Arabia +, +Jeddah +, near Thuwal, Um Alsawi, +22.239306°N +38.985139°E +, scuba, coll. +N.J. de Voogd +, field nr. THU08/JED145, + +11 November 2014 + + +; + +RMNH +Por. +9659, +Saudi Arabia +, +Jeddah +, near Thuwal, Fsar, +22.249417°N +39.002333°E +, scuba, coll. +N.J. de Voogd +, field nr. THU09/JED159, + +11 November 2014 + + +; + +ZMA +Por. +13421, +Israel +, +Gulf of Aqaba +, on pillar of containerport, depth + +5 m + +, scuba, coll. +M. Wunsch +, field nr AQ70, + +5 July 1998 + + +; + +ZMA +Por. +13422, +Israel +, +Gulf of Aqaba +, +Marsa Bareika +, depth + +20 m + +, in cave, scuba, coll. +M. Wunsch +, field nr. RM227, + +25 July 1998 + + +; + +ZMA +Por. +13429, +Israel +, +Gulf of Aqaba +, +Shark Observatory +, depth + +14 m + +, in cave, scuba, coll. +M. Wunsch +, field nr. RM241, 26 Juky 1998 + +; + +ZMA +Por. +13443, +Israel +, +Gulf of Aqaba +, on pillar of containerport, depth + +7 m + +, scuba, coll. +M. Wunsch +, field nr. AQ73, + +5 July 1998 + + +; + +ZMA +Por. +13448, +Israel +, +Gulf of Aqaba +, +Canyon +, cryptic habitat, depth + +10 m + +, scuba, coll. +M.Wunsch +, field nr. AQ137, + +14 July 1998 + + +; + +ZMA +Por. +13508, +Israel +, +Gulf of Aqaba +, +North Pinnacle +, depth + +8 m + +, in cave, scuba, coll. +M. Wunsch +, field nr. AQ56, + +4 July 1998 + + +; + +ZMA +Por. +13509, +Israel +, +Gulf of Aqaba +, +North Pinnacle +, depth + +17 m + +, in cave, scuba, coll. +M. Wunsch +, field nr. AQ33, + +4 July 1998 + + +; + +ZMA +Por. +10524, +Seychelles +, E of +Bird Island +, +3.7333°S +55.2333°E +, depth + +45 m + +, dredge, coll. +R.W.M. van Soest +, field nr + +. NIOP-E stat. 719/08, +20 December 1992 +; + +ZMA +Por. +11563, +Seychelles +, +Amirantes +, +St. François Atoll +, +Île Bijoutier +, +7.0833°S +52.7333°E +, reef, depth + +6–18 m + +, scuba, coll. +R.W.M. van Soest +, field nr + +. NIOP-E stat. 792/16, +5 January 1993 +. + + + + +Description. +Cylindrical, hairy sponges ( +Figs 68a–f +, +69a,c +), usually hanging down from ceilings or walls of reef caves. Size varies between 1 and +3 cm +high, diameter +2–10 mm +(protruding diactines included). Colors in situ varying from whitish, pale greenish, to greyish transparent; in preservation ( +Figs 69b,d +) they are light beige. Oscules are slightly constricted, lack a distinct fringe, but have a dense collar of long diactines and trichoxeas ( +Figs 68f +, +69c +), which form bundles radiating outwoards from the oscule ( +Fig. 69e +). Consistency soft. + + +Aquiferous system +. Syconoid. + + +Skeleton. +( + +Figs +68g + +, +69e–f +) Inarticulate, with the choanosomal region supported by the longer paired actines of pseudosagittal triactines and the unpaired actines of subatrial triactines. The cortical skeleton skeleton consists of large regular or slightly sagittal triactines carried by the shorter paired actines of the pseudosagittal triactines. Giant diactines are protruding far outwards from the cortex ( +Fig. 69e +) and penetrate deeply into the choanosomal skeleton contributing to the inarticulate triactine skeleton. The (sub-)atrial skeleton consists of the paired actines of subtrial triactines ( +Fig. 69f +) and smaller sagittal or oxhorn-shaped triactines. + + +Spicules. +( +Figs 70a–f +) Giant diactines, trichoxeas, cortical triactines, pseudosagittal triactines, subatrial triactines, atrial triactines. + + +Giant diactines ( +Figs 70a +), sharply pointed or with lance-head ending, 240– +903 +– +2040 x 10 +– +26.9 +–36 µm. + + +Trichoxeas ( +Fig. 70b +), invariably broken, fragments of all lengths up to +1048 x 3 +µm. + + +Cortical triactines ( +Fig. 70c +), usually more or less equiradiate and equiangular, variable in actine length within and among specimens, 181– +221 +–310 +x 14 +– +16.1 +–30 µm. + + +Pseudosagittal triactines ( +Fig. 70d +), especially variable in thickness of the actines, long paired actine straight, 246– +398 +–480 +x 14 +– +24.2 +–40 µm, short paired actine curved 105– +176 +–285 +x 13 +– +20.7 +–29 µm, unpaired actine straight or slightly curved, 107– +177 +–325 +x 14 +– +22.4 +–32 µm. + + +Subatrial triactines ( +Fig. 70e +), mostly strongly sagittal, varying from almost T-shaped to widely curved paired actines, with unpaired actine straight, tapering to thin sharp ends or occasionally bluntly rounded; unpaired actines + + +306– +436 +–620 +x 17 +– +31.1 +–46 µm, paired actines 166– +239 +–318 +x 18 +– +27.2 +–45 µm. + + +Atrial triactines ( +Figs 70f +), sagittal, often with curved paired actines; unpaired actines 68– +141 +–201 x 7.5– +10.9 +–15 µm, paired actines 72– +147 +–215 +x 9 +– +10.7 +–15 µm. + + + + +FIGURE 68. + +Sycettusa hastifera +(Row, 1909) + +, a–f, habitus in situ of various specimens from Saudi Arabia (photos N.J. de Voogd), preserved as RMNH Por. 9644, 9645 and 9659, g, light microscopic photo of cross section of RMNH Por. 9659. + + + + +Distribution and ecology. +Red Sea, +Seychelles +, Western +India +, +South Africa +, in caves and other cryptic habitats, +5–45 m +depth; records from the Southwest Atlantic ( +Lanna & Klautau 2010 +) probably concern a similar but different species of + +Sycettusa + +. + + + + +Remarks. +As indicated above, we tentatively consider + +Grantilla quadriradiata +Row, 1909 a + +synonym of + +S. hastifera + +based on examination of several slides (sections and spicule mounts) of the +holotype +incorporated in the collections of the Natural History Museum, London, under reg.nr. BMNH 1912.2.1.8a. There are no tetractines in the slides, so even if they are present in other parts of the +type +material, they are obviously a +minor +complement, probably derived from the usual pseudosagittal triactines. The + +G. quadriradiata + +spicules were at the larger part of the variation of length and thickness, but fell within it. There are no clear differences with the dozen specimens of + +S. hastifera + +present in our collection. + + + +FIGURE 69. + +Sycettusa hastifera +(Row, 1909) + +, a–d, habitus of specimens from Israel, Gulf of Aqaba, a, ZMA Por. 13429 in situ (photo M.Wunsch), b, ditto preserved, c, ZMA Por. 13508 in situ (photo M. Wunsch), d, ditto preserved, e, light microscopic photo of oscular region of ZMA Por. 13421, f, light microscopic photo of cross section of ZMA Por. 13429. + + + + +FIGURE 70. + +Sycettusa hastifera +(Row, 1909) + +, ZMA Por. 13421 from Gulf of Aqaba, a–f, SEM images of the spicules, a, lance-head diactines, a1, detail of lance-head, b, broken trichoxea, c, cortical triactine, d, pseudosagittal triactine, e, sagittal triactine, f, atrial triactines. + + + +Dendy (1913, 1916) assigned + +Grantilla +Row, 1909 + +(with species + +G. quadriradiata + +and + +G. hastifera + +) to + +Grantessa +Von Lendenfeld, 1885 + +, but that genus has been redefined by Borojević +et al. +2000, 2002b to have an articulate skeleton. Row’s species and our specimens have clearly inarticulate skeletons and thus answer to + +Sycettusa +Haeckel, 1872 + +as redefined by + +Borojević +et al. +2002b + +. + + +Three sequences available to us, two of our own and one downloaded from the Sponge Barcode Project site, all three from the Red Sea, grouped together in the same clade in the phylogeny of +Fig.3 +. + + +There are several further species of + +Sycettusa + +in our material, which will be described below and their differences with + +S. hastifera + +will be discussed in the Remarks of those species below. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC04A548FF678D6AFD68FC51.xml b/data/38/6C/C6/386CC616DC04A548FF678D6AFD68FC51.xml new file mode 100644 index 00000000000..2d21056485b --- /dev/null +++ b/data/38/6C/C6/386CC616DC04A548FF678D6AFD68FC51.xml @@ -0,0 +1,397 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Sycettusa simplex +( +Jenkin, 1908 +) + + + + + +Figs 73a–e +, +74a–f + + + + + + +Grantessa simplex + +Jenkin, 1908 +: 446 + + +, figs 93–97. + + + + +? + +Leuconia wasinensis + +; + +Burton 1959 +: 181 + +(not: +Jenkin 1908 +) + + + + + +Material examined. +RMNH +Por. 10154, +Maldives +, Faafu Atoll, Wallstreet, +3.119°N +72.979556°E +, depth +12 m +, scuba, coll. N.J. de Voogd, field nr. +MAD +10/MAS115, +20 February 2015 +; +ZMA +Por. 10338, +Seychelles +, +Mahé +, NE coast, Cap Maçons & Anse de Forbans, +4.7667°S +55.5167°E +, reef, depth +0–6 m +, snorkeling, coll. R.W.M. van Soest, field nr. +NIOP-E +stat. 612, +14 December 1992 +; +ZMA +Por. 12446, +Seychelles +, Amirantes, St. François Atoll, +7.0833°S +52.7333°E +, reef, depth +0–10 m +, snorkeling, coll. J.C. den Hartog, field nr. +NIOP-E +stat. 792(bis)/27, +4 January 1993 +. + + + + +Description. +Light beige-colored groups of longer and/or shorter tubes ( +Fig. 73a +), somewhat tangled, occasionally divided or with a side tube. Size of individual tubes up to +6 cm +or more long, +0.5 cm +wide. Surface uneven or slightly hispid. Oscules terminal, usually surrounded by a circle of diactines and/or trichoxeas. Beige color persists in alcohol ( +Figs. 73b–c +). Consistency soft, slightly firm. + + +Aquiferous system +. Syconoid. + + +Skeleton. +( +Figs. 73d–e +) Inarticulate, with a cortical skeleton of regular or slightly sagittal triactines, subectosomal pseudosagittal triactines, the long paired actines forming the choanosomal skeleton together with the unpaired actines of subatrial sagittal triactines, and with an atrial skeleton of regular or slightly sagittal triactines smaller than those of the cortical skeleton. Diactines are present in the oscular region and also occur scattered in the choanosome supporting the inarticulated skeleton. + + +Spicules. +( +Figs 74a–f +) Diactines, trichoxeas, cortical and atrial triactines, pseudosagittal triactines, sagittal triactines. + + +Diactines ( +Fig. 74a +), fusiform, usually with one end lance-headed, variable in length, 210– +701 +– +1140 x 13 +– +25.8 +–36 µm. + + +Trichoxeas ( +Fig. 74b +), small, mostly broken, 120– +182 +–235 +x 2 +– +2.4 +–3.5 µm. + + + +FIGURE 73. + +Sycettusa simplex +(Jenkin, 1908) + +, a–c, habitus of RMNH Por. 10154 from the Maldives, a, habitus in situ (photo N.J. de Voogd), b, on deck (photo N.J. de Voogd), c, preserved (scale bar = 1 cm), d, light microscopic image of cross section, e, detail of the same. + + + + +FIGURE 74. + +Sycettusa simplex +(Jenkin, 1908) + +, RMNH Por. 10154, from the Maldives, a–f, SEM images of the spicules, a, lance-headed giant diactine, b, broken trichoxea, c, cortical triactines, d, pseudosagittal triactines, e, sagittal subatrial triactines, f, atrial triactine. + + + +Cortical triactines ( +Figs. 74c +), variable in shape, from equiangular equiradiate to sagittal or irregular, actines 183– +219 +–288 +x 12 +– +17.4 +–24 µm. + + +Pseudosagittal triactines ( +Figs 74d +), in a large size range, longest actines 241– +369 +–504 +x 18 +– +21.4 +–30 µm, middle sized actines (usually the unpaired actine), 138– +186 +–228 +x 15 +– +19.7 +–30 µm, shortest actines 64– +132 +–241 +x 14 +– +18.9 +–26 µm. + + +Sagittal triactines ( +Figs 74e +), variable in shape and in thickness, paired actines often almost forming T-shape, but occasionally more acutely angled, unpaired actines 396– +436 +–538 +x 17 +– +29.6 +–44 µm, paired actines 179– +232 +–282 +x 19 +– +26.7 +–39 µm. + + +Atrial triactines ( +Fig. 74f +), regular, slightly sagittal or occasionally irregular, unpaired actine 114– +142 +–181 +x 10 +– +11.4 +–14 µm, paired actines 101– +154 +–201 +x 9 +– +10.4 +–12 µm. + + + + +Distribution and ecology. +Maldives +, +Seychelles +, + +Zanzibar + +, on reefs in shallow water. + + + + +Remarks. +Jenkin’s +type +material is closely similar both in shape and spicule sizes and shapes. Our identification with his species is made with confidence. + + +The three samples assigned here to + +S. simplex + +have similar spiculation as + +S. stauridia + +described below. The differences between the two species appear to be largely attributable to growth form, which is known to be a variable feature in many sponges. In contrast, 28S sequences of the two species were found to be substantially different (cf. +Fig. 3 +). Molecularly, + +S. simplex + +is almost identical to + +S. hastifera + +, as we found only a single site difference in the above described inspection of a trimmed alignment of 403 sites, whereas differences between + +S. simplex + +and + +S. stauridia + +numbered 22 sites. + + + +Voigt +et al. +(2012) + +sequenced a Seychelles specimen, ZMA Por. 11566 under the name + +S. simplex + +, but we reidentified this material as + +S. zanzibarensis +( +Jenkin, 1908 +) + +(see below). + + + + + +Leucortis anguinea +Ridley, 1884 + +from Providence in the Mascarene Islands is a + +Sycettusa + +according to +Burton (1963) +. It has a shape reminding a bit of the present species, but the specimen is not likely the same as the present species judging from the description in +Ridley 1884 +(p. 629, pl. 53L, 54d), as it includes tetractines. + + + +Sycettusa sibogae +( +Burton, 1930 +) + +as redescribed by Van Soest & De Voogd (2015) is similar to the present species, but has no giant diactines and its cortical triactines are twice as large. + + +We reexamined + +Leuconia wasinensis +sensu +Burton, 1959 + +from South Arabia (Murray Expedition station 45 nr. 537) kept in the Natural History Museum (BMNH 1936.3.4.537) and found this to be very similar to + +Sycettusa simplex + +. Its identity cannot be + +Leucandrilla wasinensis + +as it has a smooth tubular shape, not oval and hispid; it lacks an apical fringe and its skeleton is inarticulate. The subcortical triactines are pseudosagittal and both cortical and atrial skeleton consist of smaller triactines. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC06A547FF678892FC01FA94.xml b/data/38/6C/C6/386CC616DC06A547FF678892FC01FA94.xml new file mode 100644 index 00000000000..4cf8ea7b3af --- /dev/null +++ b/data/38/6C/C6/386CC616DC06A547FF678892FC01FA94.xml @@ -0,0 +1,381 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Sycettusa hirsutissima + +sp.nov. + + + + +Figs 71a–d +, +72a–g + + + + + +Material examined. +Holotype +, +RMNH +Por. 10004, +Saudi Arabia +, +Jeddah +, near +Thuwal +, +Tahlah +, +22.25725°N +38.880917°E +, scuba, coll. +N.J. de Voogd +, field nr. THU14/JED211, + +13 November 2014 + +. + + + + +Paratype +, +RMNH +Por. 9588, +Saudi Arabia +, +Jeddah +, near +Thuwal +, +Abu Gishaa +, +22.255194°N +39.025639°E +, depth + +12 m + +, scuba, coll. +N.J. de Voogd +, field nr. THU06/JED083, + +9 November 2014 + +. + + + + + +Description. +Densely hairy tubes ( +Figs 71a–b +), hanging down, from reef walls. Color yellow or orange below a thick pelt of diactines. In preservation they become dark grey. Size up to +8 cm +high, +0.5–1.5 cm +in diameter. Consistency firm. + + +Aquiferous system +. Syconoid. + + +Skeleton +. ( +Figs 71c–d +) Inarticulate with cortex of triactines, carried by the unpaired and shorter actines of pseudosagittal triactines. Choanosomal skeleton consists of the longer actines of the subcortical pseudosagittal triactines and the unpaired actines of sagittal subatrial triactines. Atrial skeleton consists of smaller sagittal triactines. + + + +FIGURE 71. + +Sycettusa hirsutissima + + +sp.nov +. + +, a, holotype RMNH Por. 10004, in situ on the reef off Jeddah, Saudi Arabia (photo N.J. de Voogd), b, paratype RMNH Por. 9588, ditto, c, light microscopic image of cross section of holotype, d, detail of c. + + + + +FIGURE 72. + +Sycettusa hirsutissima + + +sp.nov. + +, holotype RMNH Por. 10004, a–g, SEM images of the spicules, a, long giant diactine, b, lance-headed giant diactines, b1, detail of lance-head, c, broken trichoxea, d, cortical triactine, e, pseudosagittal triactines, f, subatrial sagittal triactines, g, atrial triactine. + + + +Spicules. +( +Figs 72a–g +) Diactines, trichoxeas, cortical triactines, subcortical pseudoaagittal triactines, subatrial triactines, atrial triactines. + + +Diactines ( +Figs 72a–b +), consisting of two types, long thin with sharp points ( +Fig. 72a +), often fragmented, + +1200– +2213 + +–3200 +x 15 +– +21.1 +–33 µm, and a shorter type with lance head endings of variable length and thickness ( +Figs 72b,b +1 +), 336– + +1179 +–2110 + +x 12– +20.3 +–30 µm. + + +Trichoxeas ( +Fig. 72c +), invariably broken into smaller pieces, 540– + +1413 +–2940 + +x 2– +2.9 +–3.5 µm. + + +Cortical triactines ( +Fig. 72d +), almost regular or slightly sagittal, 171– +202 +–261 +x 10 +– +16.0 +–18 µm. + + +Pseudosagittal triactines ( +Figs 72e +), longest actine 420– +582 +–738 +x 24 +–31.3–43 µm, shorter actine 225– +294 +–383 +x 23 +– +29.4 +–40 µm, unpaired actine 162– +207 +–299 +x 21 +– +28.8 +–42 µm. + + +Subatrial triactines ( +Figs 72f +), variably with longer and shorter unpaired actines and flat-angled or acuteangled paired actines, unpaired actines 282– +490 +–530 x 282– +36.6 +–52.5 µm, paired actines 162– +258 +–375 +x 14 +– +31.6 +–46 µm. + + +Atrial triactines ( + +Fig. +72g + +), slightly sagittal, 81– +158 +–231 +x 7 +– +13.1 +–16 µm. + + + + +Distribution and ecology. +Saudi Arabian +Red Sea +, on overhangs in shallow water. + + + + +Etymology. +Hirsutus (L.) means hairy, rough, referring to the ‘pelt’ of long protruding bundles of diactines. We use the superlative of hirsutus to emphasize the exteme hairiness. + + + + +Remarks. +The new species is close to + +S. hastifera + +in overall appearance and in spicule complement. However, the two specimens are extremely and densely hairy, unlike the dozen + +S. hastifera + +specimens we had at our disposal, which have the protruding diactines much less dense. In the new species, the body wall underneath the pelt of diactines is barely visible and has a yellow color, while it is always clearly visible and greyish or greenish white in + +S. hastifera + +. In contrast to + +S. hastifera + +the sizes (length and thickness) of the longest actine of the pseudodosagittal triactines of our new species is usually larger than that of the subatrial triactines, although this may not be of great importance. At first, we were inclined to consider the new species an extreme form of + +S. hastifera + +. However, we obtained partial 28S sequences of the two specimens (GenBank acc.nrs +MF872774 +, +MF872775 +, and +MF872776 +) and in the phylogeny of +Fig. 3 +they did not group into the same clade with + +Sycettusa hastifera + +(GenBank acc.nrs +MF872777 +of RMNH Por. 9659, and +MF872778 +of ZMA Por. 13443) and + +S. simplex +( +Jenkin, 1908 +) + +(GenBank acc. nrs +MF872779 +of RMNH Por. 10154 and +MF872781 +of ZMA Por. 12446), supporting a separation at the species level. To investigate the molecular differences between + +S. hastifera + +, + +S. hirsutissima + + +sp.nov. + +and + +S. simplex + +, we separately aligned and trimmed the available + +Sycettusa + +28S sequences of these three species yielding a length of 403 sites. The sequences of + +S. hirsitussima + + +sp.nov. + +were identical. They shared shared three site differences with + +S.hastifera + +and four with + +S. simplex + +. The latter two species differed only in a single site, despite being clearly distinct in habitus as + +S. simplex + +has an almost smooth surface (cf. below). + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC0BA54DFF678C16FC0FFDC6.xml b/data/38/6C/C6/386CC616DC0BA54DFF678C16FC0FFDC6.xml new file mode 100644 index 00000000000..d79760da0a7 --- /dev/null +++ b/data/38/6C/C6/386CC616DC0BA54DFF678C16FC0FFDC6.xml @@ -0,0 +1,398 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Sycettusa stauridia +( +Haeckel, 1872 +) + + + + + +Figs 75a–f +, +76a–f + + + + + + +Djeddea violacea +Miklucho-Maclay in + +Haeckel, 1872 +: 245 + + +( +nomen nudum +). + + + + + +Sycetta (Sycettusa) stauridia + +Haeckel, 1872 +: 236 + + +, 245, pl. 42 figs 13–16. + + + + + +Grantessa stauridia + +; + +Lévi 1965 +: 26 + +. + + + + + + + +Material +examined. + +ZMA +Por. 0 2460, +Eritrea +, +Dahlak Archipelago +, +Harmil Island +, +Red Sea +, +16.5167°N +40.15°E +, depth + +1 m + +, scuba, coll. +J.H. Stock +, +Israel + + +South +Red Sea + +Exped. + +1962, field nr. E62-10418, + +28 March 1962 + + +; + +ZMA +Por. 13664, +Israel +. Gulf of Aqaba, containerport, on pillar, depth + +5 m + +, scuba, coll. +M. Wunsch +, field nr. AQ68, + +5 July 1998 + + +. + + + + +Description. +Masses of small hollow lobes and tubes ( +Figs 75a–c +). Surface faintly roughened, not smooth. Color in situ greyish blue to light red-brown, in alcohol both samples are red-brown. Size of whole mass up to 6 + +x +8 + +cm, individual tubes and lobes up to +1.5 cm +high +1 cm +in diameter or smaller. Oscules are frequently absent from the top of the hollow lobes, as they may be at the sides or in the interstices, and are not common. They do not have observable collars or fringe and have a diameter up to +0.5 cm +. + + +Aquiferous system +. Syconoid. + + +Skeleton. +( +Figs 75d–f +) As usual, there is a cortical skeleton of triactines ( +Fig. 75e +), an inarticulated choanosomal skeleton ( +Fig. 75d +) formed by the longer paired actine of subectosomal triactines and the unpaired actines of subatrial triactines, and an atrial skeleton ( +Fig. 75f +) of tangential triactines. Rare diactines and trichoxeas. + + +Spicules. +( +Figs 76a–f +) Diactines, trichoxeas, cortical triactines, pseudosagittal triactines, large sagittal triactines, atrial triactines. + + +Diactines ( +Fig. 76a +), fusiform, supporting the inarticulated skeleton in a low frequency, 269– +426 +–541 +x 15 +– +16.6 +–19 µm. + + +Trichoxeas ( +Fig. 76b +), rare, probably associated with the oscules, 200–650 +x 2–6 +µm. + + +Cortical triactines ( +Fig. 83c +), almost regular equiangular equiradiate, 177– +213 +–255 +x 10 +– +14.0 +–20 µm. + + +Pseudosagittal triactines ( +Figs 76d +), longest actine 316– +406 +–468 +x 15 +– +18.3 +–23 µm, middle sized actine 171– +198 +–234 +x 15 +– +17.3 +–21 µm, shortest actine 108– +168 +–201 +x 15 +– +16.9 +–20 µm. + + +Subatrial triactines ( +Fig. 76e +), many are almost T-shaped, unpaired actines 328– +423 +–510 +x 24 +– +28.6 +–32 µm, paired actines 241– +272 +–336 +x 22 +– +23.7 +–27 µm. + + +Atrial triactines ( +Fig. 76f +), more ore less regular, actines 135– +159 +–174 +x 8 +– +11.1 +–13 µm. + + + + +Distribution and ecology. +Red Sea +, in shallow water. + + + + +FIGURE 75. + +Sycettusa stauridia +(Haeckel, 1872) + +, from Red Sea localities, a–c, habitus in situ and preserved, a, ZMA Por. 13664, from Israel, Gulf of Aqaba, in situ on pillar of container port (photo M. Wunsch), b, the same preserved (scale bar = 1 cm), c, ZMA Por. 0 2460 from Eritrea, habitus preserved (scale bar = 1 cm) (specimen previously reported in Lévi, 1965), d–f, SEM images of sections of the skeleton of ZMA Por. 13664 from Gulf of Aqaba, d, cross section, e, cortical skeleton, f, atrial skeleton. + + + + +Remarks. +We follow +Lévi (1965) +in assigning the specimens to Haeckel’s + +S. stauridia + +, although his figure and description shows some discrepancies: Haeckel’s specimen apparently was much smaller and he provided a stylized drawing which shows a single central tube with a ring of side tubes. He did not mention the presence of diactines. However, they are not very common in our specimens, so he may have overlooked them. He did not + +make a distinction in pseudosagittal subcortical triactines and sagittal subatrial triactines. The sizes he provided of these spicules are similar to those of the present specimens, as are those of the other spicules. + + +FIGURE 76. + +Sycettusa stauridia +(Haeckel, 1872) + +, ZMA Por. 0 2460, a–f, SEM images of the spicules, a, fusiform diactine, b, trichoxea, c, cortical triactines, d. pseudosagittal triactines, e, subatrial sagittal triactine, f, atrial triactine. + + + +There are competing names, which are potential junior synonyms of this species. Mauritian + +Sycortis sycilloides +Schuffner, 1877 + +(p. 420, pl. 25 fig. 10) has similar habitus (two coalescent small tubular individuals), but it has the unpaired actines of the subatrial triactines much longer and thicker (600–1000 +x 80 +µm) against Haeckel’s and ours only 400 +x 10–20 +µm. +Red Sea + +Grantessa glabra +Row, 1909 + +(p. 203, pl. 19 figs 5–6, text fig. 4a) is a small tube with side oscule and it has cortical and atrial triactines much larger (400–700 µm) and diactines and pseudosagittal triactines much thicker (50–90 µm) than Haeckel’s and the present material. If these measurements would prove to be inaccurate or much more variable than so far determined, these names could be synonyms. Redescription is necessary. +Burton (1959) +reported + +Grantessa glabra + +from the +South +Arabian region and + +Grantessa sycilloides + +from the Gulf of Aden, but he did not provide a description of his material. He commented that the two species, + +glabra + +and + +sycilloides + +, are probably synonymous. + + +We obtained a 28S partial sequence of one of our specimens (ZMA Por. 13664). This ended up in the same clade but rather far away from the group comprised by + +Sycettusa +hastifera-S. simplex-S. +hirsitussima + + +sp.nov. + +(cf. +Fig.3 +). As mentioned above in the Remarks of + +S. simplex + +, a trimmed alignment with a length of 403 showed 20 sites or more difference with + +S. hastifera + +, + +S. hirsutissima + +and + +S. simplex + +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC0DA5B0FF678C69FB42FC19.xml b/data/38/6C/C6/386CC616DC0DA5B0FF678C69FB42FC19.xml new file mode 100644 index 00000000000..3e2fb67cf0d --- /dev/null +++ b/data/38/6C/C6/386CC616DC0DA5B0FF678C69FB42FC19.xml @@ -0,0 +1,336 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Vosmaeropsis glebula + +sp.nov. + + + + +Figs 79a–g + + + + + +Material examined. +Holotype +, +ZMA +Por. 10608, +Seychelles +, + +La Digue Island +, S + +coast, +4.3833°S +55.8333°E +, depth + +2 m + +, reef, snorkeling, coll. +R.W.M. van Soest +, field nr + +. NIOP-E stat. 735/ +28, 23 December +1992. + + + +Paratypes +, +ZMA +Por. +10553, +Seychelles +, +Aride Island +, S coast, +4.2167°S +55.6667°E +, snorkeling, coll. +J.C. den Hartog +, field nr + +. NIOP-E stat. 711/ +12, 18 December +1992; + +ZMA +Por. +10637, +Seychelles +, +Amirantes +, +St. François Atoll +, +Île Bijoutier +, depth + +3 m + +, reef, scuba, coll. +R.W.M. van Soest +, field nr + +. NIOP-E stat. 792/ +20, 6 January +1993. + + + + +Description. +Small lobes and short thick-walled tubes ( +Fig. 79a +), occurring singly or in coalescent groups. The +holotype +consists of five such lobes, which were originally grouped together. Each lobe or tube carries a terminal oscule. Color in situ yellow-brown, in preservation they are similarly light brown. Size +1–2 cm +in height, +0.5–1 cm +in diameter, oscules about +2 mm +in diameter, flush, without rim or fringe. Consistency soft. + + +Aquiferous system +. Leuconoid. + + +Skeleton. +( +Figs 79b–c +) In our SEM cross section ( +Fig. 79b +), which is admittedly rather confused, from surface to atrium there is a cortical skeleton of smaller sagittal and larger regular triactines ( +Fig. 79c +), supported by subcortical pseudosagittal triactines replaced by giant triactines in the main skeleton. In the atrial region there are larger triactines rather similar to the cortical triactines but supported by smaller, more or less regular triactines. + + +Spicules. +( +Figs 79d–h +) Triactines only, tentatively divisible into cortical triactines, giant triactines, pseudosagittal triactines, subatrial triactines and atrial triactines. + + +Cortical triactines ( +Fig. 79d +), regular, usually with straight actines, intermediate in size, actines 76– +168 +–258 +x 8 +– +15.1 +–31 µm. + + +Pseudosagittal triactines ( +Fig. 79f +), longest actines 270– +474 +–662 +x 18 +– +36.7 +–47 µm, middle sized actines 167– +261 +–330 +x 17 +– +32.1 +–40 µm, shortest (=unpaired) actines 81– +129 +–292 +x 18 +– +32.8 +–41 µm. + + +Giant or large triactines ( +Fig. 79e +) of the main skeleton, tending to be more or less equiangular and equiradiate, 302– +567 +–779 +x 32 +– +57.4 +–78 µm. + + + +FIGURE 79. + +Vosmaeropsis glebula + + +sp.nov. + +, holotype ZMA Por. 10608 from the Seychelles, a, preserved habitus (scale bar = 1 cm), b–c, SEM images of skeleton, b, cross section through the wall, c, view of the surface skeleton, d–g, SEM images of the spicules, d, cortical sagittal triactine, e, subcortical pseudosagittal triactines, f, giant and large choanosomal triactines, g, subatrial and atrial triactines. + + + +Subatrial and atrial triactines ( + +Figs +79g + +), slightly sagittal, intermediate and smaller triactines, often with incurved paired actines; unpaired actines 93– +141 +–233 +x 15 +– +20.3 +–26 µm, paired actines 111– +195 +–271 +x 15 +– +19.6 +–24 µm. + + + + +Distribution and ecology. +Known only from several localities in the +Seychelles +, reefs, shallow water. + + + + +Etymology. +Glebula (L.) meaning small lump, referring to the habitus. + + + + +Remarks. +The new species is assigned to + +Vosmaeropsis + +on account of the confused choanosomal skeleton in combination with pseudosagittal triactines. So far, no + +Vosmaeropsis + +species are known from the Western Indian Ocean (cf. + +Cavalcanti +et al. +2015 + +; Van + +Soest +et al. +2018 + +). The new species differs from most Indo-West Pacific + +Vosmaeropsis + +species, including e.g. + +V. grisea +Tanita, 1939 + +as described by us from +Indonesia +(cf. Van Soest & De Voogd 2015), in the lack of (giant) diactines and tetractines. Only two species in that wide area share the lack of diactines and tetractines with our new species. In Philippine deeper water occurs +V. connexiva +( +Poléjaeff, 1883 +), which differs from our specimens in the apparent lack of small cortical and atrial triactines, while the pseudosagittal triactines are smaller than those of the new species, with longest actines not exceeding 400 +x 20–25 +µm (in our specimens up to 662 +x 47 +µm). The habit of the species is not clear as Poléjaeff only had a few fragments. New Caledonian + +V. hozawai +Borojević & Klautau, 2000 + +is a larger ( +5 cm +) dark brown, sac-shaped sponge from +20–25 m +depth. It differs especially in the much larger size of the giant triactines, which are up to +1500 x +100 µm (ours 779 +x 78 +µm); likewise the regular cortical and atrial triactines are larger, up to 420 +x 17 +µm (ours up to 271 +x 26 +µm). Despite the lack of illustrations for these two species, the differences are here considered sufficiently great to judge them to be different from our new species. In the area considered here there are no reports of additional + +Vosmaeropsis + +species. + + +Unfortunately, our attempt to obtain a partial 28S sequence of the +type +material failed. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC0EA54EFF678ABEFBCCFC5E.xml b/data/38/6C/C6/386CC616DC0EA54EFF678ABEFBCCFC5E.xml new file mode 100644 index 00000000000..413af345300 --- /dev/null +++ b/data/38/6C/C6/386CC616DC0EA54EFF678ABEFBCCFC5E.xml @@ -0,0 +1,509 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Sycettusa zanzibaris +( +Jenkin, 1908 +) + + + + + +Figs 77a–g +, +78a–i + + + + + + +Grantessa zanzibaris + +Jenkin, 1908 +: 448 + + +, figs 98–102; + +Burton 1959 +: 180 + +. + + + + + + + +Material +examined. + +ZMA +Por. +11491, +Seychelles +, +Bird Island +, off E coast, +3.7167°S +55.2167°E +, reef, depth + +3 m + +, snorkeling, coll. +R.W.M. van Soest +, field nr + +. NIOP-E stat. 717/ +08, 20 December +1992; + +ZMA +Por. +11566, +Seychelles +, +Amirantes +, +Île Desnoeufs +platform, outer slope, +6.2167°S +53.0167°E +, depth + +12–15 m + +, scuba, coll. +R.W.M. van Soest +, field nr + +. NIOP-E stat. 738/ +22, 2 January +1993; + +ZMA +Por. +11568, +Seychelles +, +Amirantes +, N of +D’Arros Island +, +5.4°S +53.3167°E +, depth + +45–55 m + +, on rhodolite bottom, dredge, coll. +R.W.M. van Soest +, field nr + +. NIOP-E stat. 752/ +13, 26 December +1992; + +ZMA +Por. +12438, +Seychelles +, +Amirantes +, N of +D’Arros Island +, +5.4°S +53.3167°E +, depth + +45–55 m + +, on rhodolite bottom, dredge, coll. +R.W.M. van Soest +, field nr + +. NIOP-E stat. 752/ +11, 26 December +1992. + + + + +Description. +Masses of short tubes ( +Figs 77a–b +), beige-white to light brown in situ and on deck, pale transparent white in alcohol. The specimens have a quite characteristic glassy slippery appearance in alcohol. Size of largest mass up to +2 cm +in lateral expansion, +1–2 cm +high. Individual tubes up to +5 mm +high, +3–4 mm +in diameter, with the oscule about +1 mm +diameter and surrounded by a thin collar. Consistency cartilaginous. + + +Aquiferous system +. Syconoid. + + +Skeleton. +( +Figs 77c–g +) Inarticulate ( +Figs 77c–d +). The cortical skeleton ( +Fig. 77e +) is a mixture of tangential triactines and short banana-shaped diactines, carried by the shortest paired actine and unpaired actine of subcortical pseudosagittal triactines. The inarticulate skeleton is made up of the longer actines of the subcortical pseudosagittal triactines and the unpaired actines of subatrial triactines. The atrial skeleton ( +Fig. 77f +) consists of the paired actines of the subatrial triactines supported by two +types +of tetractines, smaller with all actines of almost similar length and thickness, and larger with enlarged apical actines protruding far into the atrial lumen. The small oscular collar ( + +Fig. +77g + +) is formed by giant diactines, trichoxeas, triactines (similar to the subatrial triactines) and regular tetractines with a short apical actine. + + +Spicules. +( +Figs 78a–i +) Diactines, trichoxeas, cortical triactines, pseudosagittal triactines, sagittal triactines, tetractines. + + +Giant diactines( +Fig. 78a +), fusiform 402– +667 +– +1100 x 12 +– +20.6 +–29 µm. + + +Trichoxeas (Fig, 78b), invariably broken, fragments 240–330 +x 2–3 +µm. + + +Banana-shaped diactines ( +Fig. 78c +), curved, asymmetrical, 141– +162 +–204 +x 7 +–8.1–9 µm. + + +Cortical triactines ( +Figs 78d +), equiangular and equiradiate or more often with all actines of slightly different length or slightly sagittal, actines 84– +103 +–126 +x 6 +– +8.3 +–10 µm. + + +Pseudosagittal triactines ( +Figs 78e +), with middle actine straight or gently curved, and shortest actine with a characteristic angular curve, longest actines 81– +146 +–183 +x 6 +– +6.9 +–8 µm, middle-sized actines 73– +106 +–138 +x 6 +– +6.6 +–9 µm, shortest (unpaired) actines 59– +88 +–111 +x 6 +– +6.8 +–8 µm. + + + +FIGURE 77. + +Sycettusa zanzibaris +(Jenkin, 1908) + +, a–b, habitus of preserved specimens from the Seychelles, a, ZMA Por. 11491 (scale bar = 1 cm), b, ZMA Por. 11566 (scale bar = 1 cm), c, light microscopic image of cross section of ZMA Por. 11566, d–g, ditto, SEM images of the skeleton, d, cross section, e, cortical skeleton, f, atrial skeleton, g, skeleton of the oscular rim. + + + + +FIGURE 78. + +Sycettusa zanzibaris +(Jenkin, 1908) + +, ZMA Por. 11566, a–i, SEM images of the spicules, a, giant diactine, b. trichoxea, c, small cortical diactine, d, cortical triactines, e, pseudosagittal triactines, f, subatrial sagittal triactines, g, small atrial tetractine, h, atrial tetractine with long apical actine wjich protrudes into the atrial cavity, i, regular tetractine from the oscular rim. + + + +Subatrial triactines ( +Figs 78f +) (and triactines of the oscular collar), sagittal, almost T-shaped, unpaired actines + + +151– +179 +–210 +x 8 +– +9.8 +–11 µm, paired actines 81– +92 +–105 +x 7 +– +8.2 +–9 µm. Small equiradiate tetractines ( + +Fig. +78g + +), equiangular, but not equiradiate, with clear position of unpaired actines, paired actines and curved apical actines; unpaired actines 54– +69 +– +84 x 5 +– +6.3 +–8 µm, paired actines 76– +97 +–111 +x 6 +– +6.7 +–7 µm, apical actines 37– +56 +– +84 x 5 +– +5.7 +–7 µm. + + +Larger atrial tetractines ( +Fig. 78h +), unpaired and paired actines similar in length, 62– +95 +–112 +x 5 +–6.6–8 µm, apical actines long, curved or sometimes slightly crooked, 105– +229 +–432 +x 6 +– +7.1 +–9 µm. + + +Tetractines of the oscular collar ( + +Fig. +78i + +), resembling subatrial sagittal triactines but with small curved apical actine; unpaired actines, 81– +112 +–126 +x 7 +– +7.4 +–9 µm, paired actines 84– +96 +–111 +x 7 +–7.6–9 µm, apical actines 22– +43 +– +61 x 5 +– +5.7 +–7 µm. + + + + +Distribution and ecology +. +Seychelles +, + +Zanzibar + +, shallow water down to + +55 m +. + +Burton (1959) +reported this species from the Southern Red Sea, but provided no description. + + + + +Remarks. +The presence of tetractines and the characteristic angular curve of the unpaired actines of the pseudosagittal triactines distinguish this species from all other + +Sycettusa + +species of the Western Indian Ocean. + + + +Voigt +et al. +(2012) + +used ZMA Por. 11566 for their study of the phylogeny of Calcarea (identified as + +S. +cf. +simplex + +). Voigt +et al. +’s sequence was compared with our own from ZMA Por. 11568 (see +Fig. 74 +), and in an alignment trimmed to a length of 403 sites, we found two differences. Our partial 28S sequences of + +Sycettusa zanzibaris + +grouped in the same clade together with New Caledonian + +S. tenuis +Borojević & Klautau, 2000 + +(downloaded from the Sponge Barcode Project site) away from mainstream + +Sycettusa + +species and closer to + +Grantessa + +species. + +S. zanzibaris + +and + +S. tenuis + +were found to exhibit 3 differences in the 403 sites alignment, so these are probably closely related. +Borojević & Klautau 2000 +(p. 198) stated in their remarks that + +S. tenuis + +was ‘certainly close to + +Sycettusa simplex +( +Jenkin, 1908 +) + +’, but as these authors admit, + +S. simplex + +has no tetractines (cf. Jenkin’s description of the atrial skeleton and spicules on p. 449). Remarkably, they did not point out that + +S. zanzibaris + +rather than + +S. simplex + +is the closer species. + + +The position of the group of species comprising + +Ute +, +Uteopsis + +and + +Grantessa + +grouped in our phylogeny of +Fig. 3 +within the larger clade of + +Sycettusa + +species remains unclear for the moment. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC11A557FF678BBAFE68FD54.xml b/data/38/6C/C6/386CC616DC11A557FF678BBAFE68FD54.xml new file mode 100644 index 00000000000..55509c86082 --- /dev/null +++ b/data/38/6C/C6/386CC616DC11A557FF678BBAFE68FD54.xml @@ -0,0 +1,345 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucandra mozambiquensis + +sp.nov. + + + + +Figs 60a–f +, +61a–e + + + + +Material examined. +Holotype +, +ZMA +Por. 22408a, +Mozambique +Channel, between +Mozambique +and +Madagascar +, E of Juan de Nova +Island +, +17.2817°S +43.1567°E +, depth +60 m +, dredged, Pelagia Around Africa Exped.II, leg 6, field nr. 20 +ASC +10, 1 April +2001. + + + + +Description. +Irregular cup-shaped hollow mass ( +Fig. 60a +) with undulating unequal lumpy walls, size 5 + +x 5 x +4 + +cm, walls approximately +1 cm +thick. Color in alcohol pale brownish to dirty white. Surface rough. Inner surface of the atrial ‘hollow’ with a few oscular openings of +3–4 mm +diameter. Consistency firm but fragile. + + +Aquiferous system +. Leuconoid. + + +Skeleton. +( +Figs 60b–f +) A cross section ( +Fig. 60b +) shows a confused mass of spicules separated by a clearly developed cortical skeleton ( +Figs 60c–d +) of smaller, mostly sagittal ‘oxhorn’ triactines and a clearly developed atrial skeleton ( +Figs 60e–f +) of atrial tetractines. The choanosomal mass of spicules consists of giant triactines and smaller triactines. Near the atrial skeleton there are also sagittal subatrial tetractines recognizable by unpaired actine of length equal to the paired actines (whereas the atrial tetractines have shorter unpaired actines). + + +Spicules. +( +Figs 61a–e +) Giant triactines, smaller triactines, atrial and subatrial tetractines. + + +Giant triactines ( +Figs 61a +) of the choanosomal region, sagittal, usually with unpaired actine shorter than the paired actines, occasionally irregular with actines all of different lengths, actines relatively thin compared to other + +Leucandra + +species, 471– +903 +– +1322 x 30 +– +52.9 +–72 µm. + + +Smaller triactines ( +Figs 61b +) of the surface and the choanosome, not clearly differentiated, but either regular or more often ‘oxhorn’-like sagittal with curved and often slightly wobbly paired actines; unpaired actines 184– +258 +–346 +x 10 +– +15.6 +–26, paired actines 191– +348 +–574 +x 10 +– +15.9 +–34 µm. + + +Tetractines ( +Figs 61c–d +), sagittal, with straight unpaired actines, straight or slightly curved paired actines, and straight or slightly curved apical actines, divisible into subatrially located tetractines with unpaired actines approximately as long as the paired actines, and proper atrial tetractines with unpaired actines clearly shorter than the paired actines. + + +Subatrial tetractines ( +Fig. 61c +) with unpaired actines measuring 174– +221 +–247 +x 8 +– +11.8 +–15 µm, paired actines 187– +239 +–298 +x 11 +– +12.6 +–15 µm, apical actines 40– +55.6 +– +73 x 5 +– +6.7 +–10 µm. + + +Atrial tetractines ( +Figs 61d +) with unpaired actines 84– +108 +–151 +x 5 +– +8.8 +–12 µm, paired actines 210– +245 +–289 +x 6 +– +9.2 +–15 µm, apical actines 41– +62 +– +92 x 5 +– +6.3 +–7 µm. + + + + +FIGURE 60. + +Leucandra mozambiquensis + + +sp.nov. + +, holotype ZMA Por. 22408a, from northern Mozambique Channel, a, preserved habitus (scale bar = 1 cm), b–f, SEM images of the skeleton, b, cross section (cortical skeleton above, atrial skeleton below), c–d, view of surface and detail, e–f, view of atrial skeleton and detail. + + + + +FIGURE 61. + +Leucandra mozambiquensis + + +sp.nov +. + +, holotype ZMA Por. 22408a, from northern Mozambique Channel, SEM images of the spicules, a, giant triactines, b, cortical smaller triactines, c, subatrial tetractine, d, atrial tetractines. + + + + +Distribution and ecology. +Mozambique +Channel, on continental platform of NW +Madagascar +, depth + +60 m +. + + + + + +Etymology. +Named after the +type +locality. + + + + +Remarks. +By the absence of giant diactines, this elaborate species stands out among + +Leucandra + +species in the region. Only the above described + +L. pilula + + +sp.nov. + +shares the lack of giant diactines, but that species has radically + + +different morphology and also the spicules have different dimensions (cf. above). The new species shows morphological similarities to NE Australian + +Leucandra nicolae +Wörheide & Hooper, 2003 + +, which also lacks giant diactines and has elaborate shape, but that species has microdiactines lining the choanocyte chambers, which are not present here. The giant triactines of + +L. nicolae + +have shorter and thicker actines than the present material. + + +The tetractines of the subatrial region indicate a possible membership of the new species of the genus + +Leucandrilla + +(cf. below), because subcortical spicules in that genus include tetractines. However, the presence of the long-shafted tetractines in the present material is always close to the atrial skeleton, not in the subcortical region, and they are probably to be considered part of the atrial skeleton. + + +We obtained a partial 28S sequence of the +holotype +. In our Calcaronea phylogeny ( +Fig. 3 +), the new species grouped together with + +L. pilula + + +sp.nov. + +and + +L. nicolae + +at a modest bootstrap value (see also above under Remarks of + +L. pilula + + +sp.nov +. + +). The relationship with the other two species in the clade is not close. + + +The nearest group to + +Leucandra + +in our phylogeny ( +Fig. 3 +) is + +Paraleucilla + +, currently assigned to the family +Amphoriscidae +. The general lack of sufficient 28S sequences of Calcaronea makes this position debatable. A separate inspection of the trimmed alignment of sequences of the clade of the three + +Leucandra + +species and the two + +Paraleucilla + +species (length 423 sites) showed 37 non-conserved sites indicating a large difference between the genera (see also below). + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC14A558FF678B6CFC14FEFC.xml b/data/38/6C/C6/386CC616DC14A558FF678B6CFC14FEFC.xml new file mode 100644 index 00000000000..ad7d6a83d43 --- /dev/null +++ b/data/38/6C/C6/386CC616DC14A558FF678B6CFC14FEFC.xml @@ -0,0 +1,401 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucandrilla +aff. +intermedia +( +Row, 1909 +) + + + + + +Figs 62a–c +, +63a–h + + + + + +? + +Leucilla intermedia + +Row, 1909 +: 205 + + +, pl. 20 fig.7, textfig. 5. + + + + + +Leucandra infesta + +Dendy & Row, 1913 +: 771 + + +. + + + + + + + +Material +examined. + +ZMA +Por. 13482, +Israel +, +Gulf +of Aqaba, +Schuhmacher’s Pinnacle +, depth + +2 m + +, under dead + +Acropora + +, coll. +M. Wunsch +, field nr. AQ 126, + +10 July 1998 + +. + + + + + +Description. +Spiny-hairy, light green tube ( +Fig. 62a +) attached partially sideways to the substratum. Size +1.5 cm +in length and approximately +1 cm +in diameter. Terminal oscule naked, +3 mm +in diameter. In alcohol ( +Fig. 62b +) the specimen is dirty white. Consistency firm. + + +Aquiferous system +. Syllebeid. + + +Skeleton. +( +Fig. 62c +) In cross section, the skeleton of the wall shows a cortical layer of small triactines pierced by giant diactines, subcortical skeleton of sagittal large tetractines, choanosomal and subatrial giant, intermediate and small triactines and tetractines, and atrial sagittal triactines and tetractines. The oscular collar contains trichoxeas. + + +Spicules. +( +Figs 63a–h +) Diactines, triactines, tetractines, trichoxeas, + + +Giant diactines ( +Figs 63a,a +1 +) fusiform, tapering to thin points, more or less equiended, + +1000– +2313 + +–4680 +x 24 +– +44.3 +–50 µm + + +Cortical triactines ( +Fig. 63b +), slightly sagittal, but equiactinal, 81– +114 +–141 x 7.5– +9.3 +–11 µm + + +Subcortical large tetractines ( +Fig. 63c +) with apical actines longest and protruding into the choanosome, with unpaired actines 225– +276 +–405 +x 18 +–28.1–44 µm, paired actines 152– +238 +–324 +x 15 +–21.6–30 µm, and apical actines 37– +184 +–390 +x 9 +– +21.0 +–42 µm. + + +Large triactines ( +Fig. 63d +) and intermediate forms from the choanosomal and subatrial region, slightly sagittal, 165– +364 +–570 +x 15 +– +30.9 +–51 µm. + + +Large tetractines ( +Fig. 63e +) from the choanosomal and subatrial region, slightly sagittal, unpaired actines 129– +227 +–345 +x 15 +– +22.5 +–34 µm, paired actines 153– +249 +–324 +x 12 +– +17.8 +–24 µm, apical actines 37– +53 +– +62 x 8 +– +14.3 +–19 µm + + +Atrial triactines ( +Fig. 63f +), sagittal, unpaired actines 63– +137 +–181 +x 7 +– +8.8 +–11 µm, paired actines 141– +161 +–174 +x 6 +– +8.6 +–12 µm. + + +Atrial tetractines ( + +Fig. +63g + +), sagittal, with thin sharp apical actines, unpaired actines 96– +119 +–148 +x 10 +–12.0–16 µm, paired actines 123– +154 +–186 +x 10 +– +10.8 +–14 µm, apical actines 15– +26.3 +– +37 x 6 +– +8.3 +–12 µm. + + +Trichoxeas ( +Fig. 63h +), invariably broken, 800– +1000 x 3 +–3.5 µm. + + + + +FIGURE 62. + +Leucandrilla +aff. +intermedia +(Row, 1909) + +, ZMA Por. 13482, from Gulf of Aqaba, a, habitus in situ (photo M. Wunsch), b, preserved habitus of same (scale bar = 1 cm), c, light microscopic view of peripheral skeleton. + + + + +Distribution and ecology. +Red Sea +, shallow depth. + + + + +Remarks. +The above-described specimen conforms in most details to Row’s description and figures of specimens from +Suez +. There are slight discrepancies in the spicule sizes, but these are rather generalized in Row’s treatment, so this is of not much concern. In contrast to Row’s description there are triactines among the atrial spicules in our specimen, which throws some doubt on our identification, hence our assignment to + +aff. +intermedia + +. It cannot be excluded that our material belongs to a different closely similar species. + + +Dendy & Row’s (1913) new name + +Leucandra infesta + +for the secondary homonymy of Row’s + +Leucilla intermedia + +with Haeckel’s (1872) + +Leucetta paradoxa +var. +intermedia + +has become moot, because the two species involved are now reassigned to different genera. Since the replacement name + +L. infesta + +was only used once in Burton’s (1963) summary of Row’s description, which does not count as ‘use’ in the sense of ICZN art. 59.3, the name + +L. intermedia + +is reinstated. + + + +FIGURE 63. + +Leucandrilla +aff. +intermedia +(Row, 1909) + +, ZMA Por. 13482, from Gulf of Aqaba, a, giant diactine, a1, detail of ending of the same, b, cortical oxea, c, subcortical tetractines, d, large triactine, e, subatrial tetractine, f, atrial triactine, g, atrial tetractine, h, trichoxea (fragment). + + + +Unfortunately, we were unable to obtain partial 28S sequence data. To investigate the likely position of the genus + +Leucandrilla + +in our phylogeny of +Fig. 3 +, we obtained sequences of a + +Leucandrilla + +spec. (GenBank acc.nrs. +MF872768 +, +MF872769 +, +MF872770 +and +MF872771 +) from the Galapagos Islands. We included these in a separate analysis of the combined Galapagos and all other Calcaronea sequences, with the result that the Galapagos + +Leucandrilla + +grouped in the same clade with the above mentioned + +Leucandra + +sequences, at a low bootstrap value (42%). We do not show this result because we did not obtain +Western +Indian Ocean or +Red Sea +sequences of + +Leucandrilla + +to compare them with, but mention this examination to confirm that + +Leucandrilla + +and + +Leucandra + +are likely more closely related to each other than either is to other Calcaronea. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC1BA558FF6789B2FB86F81A.xml b/data/38/6C/C6/386CC616DC1BA558FF6789B2FB86F81A.xml new file mode 100644 index 00000000000..14cfbf9ec35 --- /dev/null +++ b/data/38/6C/C6/386CC616DC1BA558FF6789B2FB86F81A.xml @@ -0,0 +1,334 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucandrilla wasinensis +( +Jenkin, 1908 +) + + + + + +Figs 64a–e +, +65a–g +. + + + + + + +Leucilla wasinensis + +Jenkin, 1908 +: 454 + + +, figs 104A–B. + + + + +Leucandra wasinensis + +; Dendy 1913: 24, pl. 2 fig. 5. + + + + +( +Not: + +Leuconia wasinensis + +; +Burton 1959 +: 181 = + +Sycettusa +cf. +simplex + +). + + + + + + +Material +examined. + +ZMA +Por. 11561, +Seychelles +, +Amirantes, N +of +Poivre island +, +5.7°S +53.3°E +, depth + +42–45 m + +, calcareous gravel bottom + +, +2.4 m +Agassiz trawl, coll. R.W.M. van Soest, field nr. NIOP-E stat. 776/ +21, 31 December +1992. + + + + +Description. +White, sycon-like sponge ( +Fig. 64a +), with prominent fringe and hairy surface. Size +2 cm +high, +1.2 cm +in diameter, atrial lumen +1–2 mm +in diameter. Consistency firm. + + +Aquiferous system +. Leuconoid. + + +Skeleton. +( +Figs 64b–e +) The cortical region ( +Figs 64b–c +) consists of a layer of smaller triactines covering a layer of subcortical tetractines. The cortical skeleton is pierced by single giant diactines causing the hispidation. The main skeleton ( +Fig. 64b,d +) contains a mass of large and small triactines, and some tetractines. The atrial skeleton ( +Fig. 64d +) consists of smaller tri- and tetractines. The fringe ( +Fig. 64e +) consists of a mixture of giant diactines, trichoxeas and sagittal tri– and tetractines. + + +Spicules. +( +Figs 65a–g +) Triactines, tetractines, giant diactines, trichoxeas. + + +Large triactines ( +Fig. 65a +), equiangular, usually slightly sagittal, actines 286– +340 +–448 +x 21 +– +30.9 +–38 µm. + + +Smaller cortical and choanosomal triactines ( +Fig. 65b +), 210– +241 +–279 +x 18 +– +25.5 +–31 µm. + + +Smaller choanosomal and subatrial triactines ( +Fig. 65c +), sagittal or irregular, unpaired actines 122– +170 +–203 +x 14 +– +18.1 +–22 µm, paired actines 63– +171 +–249 +x 12 +– +16.4 +–21 µm. + + +Large subcortical tetractines ( +Figs 65d +), sagittal, unpaired actines 212– +389 +–521 +x 11 +– +20.4 +–26 µm, paired actines 116– +194 +–252 +x 10 +– +17.6 +–24 µm, apical actines 12– +49 +– +66 x 4 +– +5.9 +–9 µm. + + +Small atrial tetractines ( +Figs 65e +), sagittal, with curved paired actines, and straight or curved apical actines; unpaired actines 32– +97 +–164 +x 4 +– +8.7 +–14 µm, paired actines 49– +105 +–136 +x 4 +– +8.4 +–11 µm, apical actines 38– +61 +–112 +x 4 +– +7.2 +–10 µm. + + +Trichoxeas ( +Fig. 65f +), straight, thin, invariably broken in the slides, fragments 200–515 +x 2–5 +µm. + + +Giant diactines ( + +Figs +65g + +), curved, endings tapering to sharp points, + +1390– +2072 + +– +2520 x 20 +–52.3–62 µm. + + + + +Distribution and ecology. +Seychelles +, Wasini Island off +Kenya +, Saya de Malha, on gravelly bottom at greater depth (> +40 m +). +Burton (1959) +reported + +Leuconia wasinensis + +from the South Arabian region ( +38 m +), but he did not provide a description. Its identity was re-examined and the record is reassigned here, see below. + + + + +Remarks. +The specimen described above resembles previous descriptions of +Jenkin (1908) +and Dendy (1913) in most details. Jenkin’s material had the larger triactines up to 950 +x 40 +µm (in our material 448 +x 38 +µm). Likewise, the subcortical tetractines of Jenkin’s specimen were larger, up to 700 +x 28 +µm (ours 521 +x 26 +µm), and also the atrial tetractines were considerably larger than ours. Dendy’s (1913) decription lacks detailed spicule measurements, but he admits that the spicules of his specimen were ‘a good deal smaller’ than Jenkin’s. We assume here that spicule sizes are subject to variation. + + +Burton (1959) +recorded this species (as + +Leuconia + +), but after re-examination this was found to be very similar to + +Sycettusa simplex +( +Jenkin, 1908 +) + +, see the Remarks of that species below. + +Unfortunately, our attempt to obtain partial 28S sequences of this species failed. + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC1DA541FF678BF2FCCEFF61.xml b/data/38/6C/C6/386CC616DC1DA541FF678BF2FCCEFF61.xml new file mode 100644 index 00000000000..b6dd91f1692 --- /dev/null +++ b/data/38/6C/C6/386CC616DC1DA541FF678BF2FCCEFF61.xml @@ -0,0 +1,245 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + +Genus + +Sycettusa +Haeckel, 1872 + + + + + + + + + +Sycetta (Sycettusa) + +Haeckel, 1872 +: 236 + + + + + + +? + +Grantilla + +Row, 1909 +: 187 + + +; + + +Borojević +et al. +2002b + +: 1176 + +. + + + + + +Remarks. +According to the Systema Porifera, chapter on the order +Leucosolenida +by + +Borojević +et al. +2002b + +, + +Sycettusa +Haeckel, 1872 + +and + +Grantilla +Row, 1909 + +, differ only in the presence in the latter of pseudosagittal tetractines in addition to pseudosagittal triactines. We borrowed two slides of the +type +specimen of + +Grantilla quadriradiata +Row, 1909 + +from the collections of the Natural History Museum, London, BMNH 1912.2.1.8a. This species is the +type +and only member of the genus + +Grantilla + +recognized by + +Borojević +et al. +2002b + +. The slides consisted of sections and dissociated spicule mounts. Remarkably these did not contain a single recognizable subcortical pseudosagittal tetractine, but instead had only pseudosagittal triactines (called ‘prochiacts’ by Row). There was not a single tetractine in the borrowed material, despite its alleged occurrence in the extensive description of +Row (1909, p. 198) +. We studied a number of + +Sycettusa + +specimens answering to the description of + +Grantilla hastifera +Row, 1909 + +, and these are not separable from the studied +type +material of + +Grantilla quadriradiata + +. We propose to consider + +Grantilla + +a junior synonym of + +Sycettusa + +because even if Row’s material ultimately will be found to contain a few quadriradiate pseudosagittal spicules, their rarity and overall similarity with + +Sycettusa hastifera + +is hardly a difference meriting generic distinction. + + + + + +Sycettusa + +was erected by +Haeckel (1872) +, as a subgenus of his genus + +Sycetta + +, for type species + +Sycetta stauridia +Haeckel, 1872 + +, but subsequently he refrained from using the combination. He did use a further combination + +Sycothamnus stauridia + +in his confusing artificial system as a ‘generische Individualität’, a remnant from his 1870 Prodomus, which is hopefully to be suppressed in the near future as a source for named sponge taxa. + + +A further issue in the genus + +Sycettusa + +is the lack of differentiation in the complement of the spicules and their sizes and shapes in many forms that differ distinctly in habitus (color, shape, size, oscular openings and protruding diactines). Apparently, overall shape is an important marker for species recognition. + + + + +We obtained several partial 28S sequences of members of the genus, some of which tend to support specific distinction of specimens showing very little differentiation in their spicule complement. The genus appears to be non-monophyletic in our phylogeny of +Fig. 3 +, with + +Sycettusa zanzibaris +( +Jenkin, 1908 +) + +and New Caledonian + +S. tenuis +Borojević & Klautau, 2000 + +grouped with + +Grantessa +cf. +intusarticulata + +, separated from a predominantly Red Sea group of + +Sycettusa + +species by + +Grantessa woerheidei + +, and + +Uteopsis + +and + +Ute + +. As argued above, the small number of Calcaronea partial 28S rRNA sequences, may be responsible for this inconsistent result. Nevertheless, it may be possible that + +Sycettusa + +is genuinely non-monophyletic. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC1EA55EFF67892FFDD7FC3D.xml b/data/38/6C/C6/386CC616DC1EA55EFF67892FFDD7FC3D.xml new file mode 100644 index 00000000000..73df4ee4ab1 --- /dev/null +++ b/data/38/6C/C6/386CC616DC1EA55EFF67892FFDD7FC3D.xml @@ -0,0 +1,468 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Grantessa woerheidei + +sp.nov. + + + + +Figs 66a–f +, +67a–g + + + + + + +Material +examined. + +Holotype +, +RMNH +Por. 9586, +Saudi Arabia +, +Jeddah +, near +Thuwal +, +Abu Gishaa +, +22.255194°N +39.025639°E +, depth + +12 m + +, scuba, coll. +N.J. de Voogd +, field nr. THU06/JED081, + +9 November 2014 + +. + + + + + +Description. +Extremely ‘hairy’ sycon-like ovoid sponge ( +Figs 66a–b +), whitish in situ, light beige in preservation. Size +2 cm +high, +0.5 cm +in diameter ( +1 cm +if protruding diactines are included). Consistency compressible but firm. + + +Aquiferous system +. Syconoid. + + +Skeleton. +( +Figs 66c–f +) Articulate, with radiating structure following the syconoid aquiferous system. The wall of the sponge is pierced almost for its entire thickness by long giant diactines, and these protrude beyond the surface for a considerable distance. From the periphery to the atrial cavity there is first a thin cortical layer of small triactines, overlying a layer of pseudosagittal triactines, with the unpaired and short paired actine tangential to the surface and the long paired actine directed inwards. Next, the choanosomal skeleton ( +Figs 66c–d +) consists of aligned tracts of sagittal tubar triactines with the unpaired actines directed outwards and the paired actines similarly aligned parallel to the cortical and atrial surfaces. Below this, the subatrial skeleton is formed by triactines similar to the tubar triactines but with unpaired actines elongated, also directed outwards. Finally, the atrial skeleton is formed by the basal triadiate system of tetractines, with their apical actines protruding far into the atrial cavity ( +Fig. 66d +). Although there is not a separate fringe, the oscular opening is surrounded by protruding diactines ( +Fig. 66e +) even longer than those of the main body, and these also form bundles, which give the opening a star-like appearance. The oscular rim is strengthened by rows of triactines ( +Fig. 66f +) + + +Spicules. +( +Figs 67a–g +) Diactines, triactines, pseudosagittal triactines, tetractines. + + +Giant diactines ( +Figs 67a,a +1 +), long, straight, varying in thickness from trichoxea-like thin diactines to thickly fusiform longer and shorter spicules, with endings varying from thinly sharply tapering to lance-shaped, those protruding from the main body 700– +2791 +–4900 +x 4 +– +25.8 +–33 µm, the oscular diactines are at least +6–7 mm +x 3–20 +µm. + + +Triactines of the oscular rim ( +Fig. 67b +), sagittal, rather strongly recurved, only a few could be measured, actines 70–130 +x 7–10 +µm. + + +Triactines of the cortical skeleton ( +Figs 67c +), slightly sagittal, actines 62– +111 +–145 +x 5 +– +7.6 +–9 µm. + + +Pseudosagittal triactines ( +Figs 73d +), of variable shape but always clearly distinct from other triactines by having all actines of different length and usually partially curved, unpaired actines 86– +112 +–132 +x 5 +– +6.2 +–7.5 µ, long paired actines 92– +189 +–244 +x 5 +– +6.0 +–7.5 µm, short paired actines 36– +48 +– +65 x 5 +– +5.7 +–7 µm. + + +Tubar triactines ( +Figs 67e +), sagittal, equiangular, unpaired actines 110– +124 +–146 +x 5 +– +7.6 +–11 µm, paired actines 84– +125 +–193 +x 5 +– +7.1 +–10 µm. + + +Subatrial triactines ( +Fig. 67f +), sagittal, equiangular, with unpaired actine longer than paired actines, measuring 195– +223 +–285 +x 5 +–7.7–11 µm, paired actines 63–110–132 +x 4 +– +6.4 +–10 µm. + + +Atrial tetractines ( + +Figs +67g + +), with slightly curved actines, often with apical actines longest; unpaired actines 102– +134 +–186 +x 4 +–5.6–8 µm, paired actines 99– +144 +–180 +x 4 +–5.3–7 µm, apical actines 46– +155 +–345 +x 3 +– +5.3 +–10 µm. + + + + +Distribution and ecology. +Saudi Arabia +, +Red Sea +, from shallow-water reef overhangs. + + + + +Etymology. +Named after Professor Gert Wörheide, München, to acknowledge his important contributions to Calcarea systematics. + + + + +Remarks. +On paper this species appears close to Southeast Australian + +Grantessa hirsuta +( +Carter, 1886 +) + +(originally as + +Hypograntia + +), as redescribed by +Dendy (1893a) +and +Burton (1963: 461) +. Unfortunately there are no images of this species published so far. From the description it is clear that it is a small cylindrical sponge (about +2 cm +high) with hispid surface and apical fringe. However, the details provided by the latter two authors show several distinct differences with our new species: (1) the diactines protruding from the surface are given as 500– +1000 x 14 +µm, against up to 7000 +x 35 +µm in our specimen, (2) the apical actines of the atrial tetractines are given as up to 100 +x 6 +, against up to 345 +x 10 +µm in our specimen, (3) the articulated skeleton is described as being irregular, whereas our specimen has a very regular tubar skeleton. The lack of differentiation in the various kinds of tri- and tetractines provided in these descriptions makes it hard to be certain of the value of these differences. At least, the length of the diactines and the atrial apical actines provide quite a different aspect in the skeletal structure. The geographic distance and temperature discrepancy between temperate SE Australian waters and the tropical +Red Sea +adds a further argument for specific distinctness. + + + +FIGURE 66 +. + +Grantessa woerheidei + + +sp.nov. + +, holotype RMNH Por. 9586 from Saudi Arabia, Red Sea, a–b, habitus in situ from above and from the side (photos N.J. de Voogd), c–f, light microscopic images of skeleton, c, cross section, d, detail of c, showing choanosomal and atrial region, e, view of oscular region, f, detail of oscular rim. + + + + +FIGURE 67 +. + +Grantessa woerheidei + + +sp.nov. + +, holotype RMNH Por. 9586 from Saudi Arabia, Red Sea, SEM images of the spicules, a, giant diactine with pointed apices, a1, smaller diactine with lance head, b, triactine of the oscular rim, c, triactines of the cortical skeleton, d, pseudosagittal triactines of the subcortical region, e, tubar triactines, f, subatrial triactines, g, atrial tetractines. + + + +There is a possibility that our new species was previously recorded from the +Gulf +of +Aden +by +Burton (1959) +under the name + +Grantessa sycilloides +( +Schuffner, 1877 +) + +. We reexamined Burton’s specimen (Murray Expedition station 24, nr 538) in 2004 and from our notes found this to be close in spiculation: giant diactines protruding from the surface, cortical skeleton of small triactines, an articulate main skeleton of pseudosagittal and sagittal triactines, and atrial skeleton of tetractines. In alcohol the specimen was brownish, shaggy. It is certainly unlike + +Sycortis sycilloides +Schuffner, 1877 + +, as this is largely smooth and does not have atrial tetractines. Schuffner’s species could be a junior synonym of + +Sycettusa stauridia + +(see below), but this remains undecided. + + +The genus + +Grantessa + +is large. In our recent paper on Indonesian Calcarea, in which we described two new species, we discussed most of the species occurring in the Indo-West Pacific. We refer to this paper (pp. 82–86) for the more distantly distributed species. The two Indonesian species ( + +G. borojevici +Van Soest & De Voogd, 2015 + +and + +G. tenhoveni +Van Soest & De Voogd, 2015 + +) are clearly distinct from + +G. woerheidei + + +sp.nov. + +in having a smooth surface (with only small diactines in the cortical region) and both comprise coalescent groups of individuals. Additionally, they differ in details of their spiculation. The small diactines mentioned for the Indonesian species also occur in the widespread, smooth-surfaced + +G. intusarticulata +( +Carter, 1886 +) + +(originally as + +Hypograntia + +) and the +South +African + +G. rarispinosa +Borojević, 1967 + +. The latter two species lack tetractines. + +G. ramosa +( +Haeckel, 1872 +) + +(originally as + +Sycandra + +) as described by +Borojević (1967, p. 204) +from + +South +Africa + +forms a group of coalescent individuals and has sagittal triactines with long swollen unpaired actines and tetractines likewise with swollen apical actines. +No +other + +Grantessa + +species are known from the region. + + +We obtained a partial 28S sequence of this specimen. In our Calcarea phylogeny of +Fig. 3 +, which included a + +Grantessa +cf. +intusarticulata + +sequence downloaded from the Sponge Barcode Project, + +Grantessa woerheidei + + +sp.nov. + +ended up in a mixed larger clade quite close to Indonesian + +Uteopsis argentea +( +Poléjaeff, 1883 +) + +, away from + +Grantessa +cf. +intusarticulata + +. In a trimmed alignment of three identical + +Uteopsis argentea + +sequences and one + +Grantessa woerheidei + +sequence of 428 sites, only 5 sites were found to be different, indicating that the two are inexplicably close. + +Voigt +et al. +(2012) + +already found that the family monophyly of +Heteropiidae +could not be retrieved resulting in two +Heteropiidae +groups separated by some +Jenkinidae +. Clearly, more taxa are needed to sort out the relationships of + +Grantessa + +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC23A562FF678C4AFC37F81D.xml b/data/38/6C/C6/386CC616DC23A562FF678C4AFC37F81D.xml new file mode 100644 index 00000000000..3b598c2077d --- /dev/null +++ b/data/38/6C/C6/386CC616DC23A562FF678C4AFC37F81D.xml @@ -0,0 +1,294 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucetta pyriformis +Dendy, 1913 + + + + + +Figs 47a–c +, +48a–e + + + + + +Leucetta pyriformis +Dendy, 1913: 11 + +, pl. 1 fig. 7, pl. 4 fig. 3. + + + +? + +Leucetta microraphis + +; + + +Voigt +et al. +2017 + +: 21 + +, figs 12a–d (cf. below). + + + + + +Material examined. +RMNH +Por. 9528, +Saudi Arabia +, Jeddah, near Thuwal, Shi'b Nazer (exposed), +22.303417°N +39.048917°E +, depth +6 m +, scuba, coll. N.J. de Voogd. field nr. THU02/JED011, +6 November 2014 +;? +ZMA +Por. 10461, +Seychelles +, +Mahé +, NE coast, +North +East Point, +4.5833°S +55.4667°E +, depth +0–5 m +, snorkeling, coll. R.W.M. van Soest, field nr. +NIOP-E +stat. 604, +8 December 1992 +. + + + + +Description. +In situ these are globular to lobate, white-transparant sponges ( +Figs 47a–b +), with at the surface giant triactines clearly visible to the naked eye. There is a narrow atrial cavity in the center of the lobes, ending in an oscule with small rim. Largest individual lobe +3 cm +high, +2 cm +in diameter. Preserved fragments ( +Fig. 47c +) are yellowish white in color and rough looking and feeling. Consistency firm to hard. + + +Aquiferous system +. Leuconoid. + + +Skeleton. +Dense mass of triactines, with giant triactines especially numerous at the surface, and with tetractines at the atrial surface. + + + +Spicules. +Giant triactines, small triactines, and tetractines. The Saudi Arabian material is slightly different from the +Seychelles +material and both differ slightly from Dendy’s +type +specimens from +Cargados Carajos +, so we provide spicule data for all specimens separately. + + + +RMNH Por. 9528: Giant triactines ( +Fig. 48a +), equiradiate, equiangular, 504– +1073 +–1711 +x 61 +– +131.8 +–204 µm; ZMA Por. 10461: 354– +852 +–1470 +x 42 +– +109.8 +–181 µm; Dendy (1913): +1000 x +100 µm. + + +RMNH Por. 9528: Small triactines ( +Figs 48b +), equiradiate, equiangular, 102– +191 +–234 +x 11 +– +14.9 +–24 µm, some smaller sagittal triactines ( +Fig. 48c +) with wavy paired actines may represent spicules from the oscular rim; ZMA Por. 10461: 132– +182 +–222 +x 11 +– +14.8 +–19 µm; Dendy (1913): 170 x 12.5 µm, including some sagittal triactines. + + +RMNH Por. 9528: Tetractines, ( +Fig. 48d +) basal radiate system similar to triactines, but actines smaller and thinner, 121– +152 +–184 +x 8 +– +11.7 +–14 µm; apical actines ( +Fig. 48e +) relatively long, straight, sharply pointed, 47– +99 +–146 +x 3 +– +8.1 +–11 µm; ZMA Por. 10461, respectively 133–161–201 +x 9 +– +12.9 +–17 µm and 41–118–164 +x 5 +– +9.2 +–11 µm; Dendy (1913): similar in size to triactines, apical actine long and slender. + + + + +FIGURE 47. + +Leucetta +pyrifomis +Dendy, 1913 + +, RMNH Por. 9528 from Saudi Arabia, Jeddah, a–b, habitus in situ (photos N.J. de Voogd), c, preserved fragments. + + + + +FIGURE 48. + +Leucetta +pyrifomis +Dendy, 1913 + +, RMNH Por. 9528 from Saudi Arabia, Jeddah, SEM images of the spicules, a, giant triactine, b, small triactines, c, cortical sagittal triactine, d, tetractine, e, detail of tetractine showing long thin straight apical actine. + + + + +Distribution and ecology. +Saudi Arabia +, +Seychelles +, +Cargados Carajos +, on reefs at shallow depth. +Burton (1959) +reported this species from the +Maldives +, but provided no description. + + + + +Remarks. +Dendy’s (1913) +type +material is similar in shape (although slightly smaller) and also has the giant triactines clearly visible at the surface (cf. Dendy 1913: pl.1 fig. 7). The white live color was not recorded by Dendy. The combination of characters differs clearly from + +Leucetta chagosensis + +(yellow, smooth, with clearly thinner giant triactines, and the apical actines of the tetractines usually curved) and + +L. microraphis + +(red-browngreenish, apical actines of the tetractines thin and usually curved). + + + +Voigt +et al. +’s (2017) + +record of + +L. microraphis + +consisted of pinkish white lobes, with prominent oscules. The transparent surface shows giant triactines like in our material, and the apical actines of the tetractines are long, up to 180 +x 13 +µm, so we assume that their record could belong to the present species. + +Unfortunately we were not succesfull in obtaining partial 28S sequences. + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC24A569FF678DBBFC91FB89.xml b/data/38/6C/C6/386CC616DC24A569FF678DBBFC91FB89.xml new file mode 100644 index 00000000000..48c12bcb4e8 --- /dev/null +++ b/data/38/6C/C6/386CC616DC24A569FF678DBBFC91FB89.xml @@ -0,0 +1,351 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Pericharax orientalis +Van Soest & De Voogd, 2015 + + + + + +Figs 51a–h + + + + + + +Pericharax heteroraphis + +; sensu Dendy 1913: 13 (not: + +Pericharax carteri +var. +heteroraphis + +Poléjaeff, 1883 +: 66 + + +). + + + + +Pericharax orientalis +Van Soest & De Voogd, 2015: 57 + +, figs 41a–e, 42a–e. + + + + + + +Material +examined. + +RMNH +Por. +10157, +Maldives +, +Faafu Atoll +, +Wallstreet +, +3.119°N +72.979556°E +, depth + +12 m + +, scuba, coll. +N.J. de Voogd +, field nr + +. MAD10/MAS118, +20 February 2015 +; + +ZMA +Por. +17996, +Mauritius +, +20.0304°S +57.5364°E +, depth + +7–28 m + +, scuba, coll. +P. Daniel Marie +, field nr. MO4SP5TB, 2014 + +; + +ZMA +Por. +18308, +Mauritius +, +20.0378°S +57.5361°E +, depth + +10–20 m + +, scuba, coll. +P. Daniel Marie +, field nr. 5, + +December 2014 + + +; + +ZMA +Por. +21792, +Mauritius +, depth + +10–20 m + +, scuba, coll. +P. Daniel Marie +, field nr. VI sp.17, + +December 2010 + + +. + + + + +Description. +Since this species was treated extensively recently (see Van Soest & De Voogd, 2015), we provide here only a short description. Large, yellow-green, upright or volcanoe-shaped sponges ( +Fig. 51a +), with faintly ridged or shallowly grooved sides and prominent wide central vent or oscule. Occasionally two or more individuals are attached forming a small group. Sizes up to +10 cm +or more in height, +10 cm +or more in diameter. Surface may be covered in tiny tubes of syllid worms. In preservation, specimens become red-brown ( +Fig. 51b +). Consistency hard, rough to the touch. + + + +FIGURE 51. + +Pericharax orientalis +Van Soest & De Voogd, 2015 + +, RMNH Por. 10157, from the Maldives, a, habitus in situ (photo N.J. de Voogd), b, on deck, c, cross section of atrial wall to show apical actines of the tetractines protruding in the atrial lumen, d–h, SEM images of the spicules, d, giant triactine, e, cortical triactine, f, small triactine, g, tetractine, h, detail of g showing thin apical actine. + + + +Aquiferous system +. Leuconoid. + + +Skeleton. +Cortical region with a thin layer of small sagittal triactines forming rounded subdermal spaces, carried by tangentially arranged subcortical giant triactines. Choanosomal skeleton built predominantly by small triactines supporting the leuconoid canal system. The atrial walls are formed predominantly by tetractines with their apical actines protruding into the atrial cavity ( +Fig. 51c +). + + +Spicules. +( +Figs 51d–h +) Giant triactines, small cortical triactines, small choanosomal triactines, atrial tetractines. + + +Giant triactines ( +Fig. 51d +), equiradiate, equiangular, 396– + +1386 +–2310 + +x 28– +124.3 +–222 µm. + + +Cortical triactines ( +Fig. 51e +), irregular, slightly sagittal, with all three actines slightly different and somewhat wavy, 54– +88 +–119 +x 6 +– +8.1 +–11 µm. + + +Small triactines ( +Fig. 51f +), regular, equiradiate, equiangular, 126– +181 +–228 +x 12 +– +15.9 +–23 µm. + + +Tetractines ( + +Figs +51g +–h + +), with basal radiate system equiradiate, equiangular, actines 106– +156 +–192 +x 7 +– +11.3 +–17 µm, apical actines ( +Fig. 51h +) thin, mostly wavy or curved, but may be straight, 25– +67 +–108 +x 4 +– +6.4 +–10 µm. + + + + +Distribution and ecology. +Maldives +, +Mauritius +, elsewhere widely distributed in the Indo-West Pacific tropical region, on reefs down to +20 m +or deeper. + + + + +Remarks. + +Pericharax peziza +Dendy, 1913 + +is a small cup-shaped sponge, pale yellow in alcohol, which has not been found again after its original description from +Cargados Carajos +. Its skeletal architecture and spiculation is similar to + +P. orientalis + +. + + +We obtained sequences of the +holotype +of + +Pericharax orientalis + +from +Indonesia +(RMNH Por. 5259) and of the above described RMNH Por 10157 from the +Maldives +and in our phylogenetic analysis ( +Fig. 2C +) both ended up in the same clade at moderate bootstrap value. + + +Recently, Leocorny +et al. +(2017) described several new + +Pericharax + +species from Western Australia, + +P. vallii +Leocorny +et al. +, 2017 + +, and + +P.crypta +Leocorny +et al. +, 2017 + +. These species clearly differ from the present specimens in aspects of habitus and spicule sizes. Leocorny +et al. +(2017) found that + +Leucetta + +and + +Pericharax + +could not be retrieved as monophyletic, and this is confirmed in our +Fig. 2C +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC26A564FF678892FF38FE6D.xml b/data/38/6C/C6/386CC616DC26A564FF678892FF38FE6D.xml new file mode 100644 index 00000000000..db58e892af2 --- /dev/null +++ b/data/38/6C/C6/386CC616DC26A564FF678892FF38FE6D.xml @@ -0,0 +1,490 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucetta sulcata + +sp.nov. + + + + +Figs 49a–d +, +50a–d + + + + + + +Material +examined. + +Holotype +, +RMNH +Por. 11639, +Mauritius +, +Rodrigues +, +Mourouk Ebony +, +Castel Rock +, +19.76203°S +63.46273°E +, depth + +10 m + +, scuba, coll. +N.J. de Voogd +, field nr. ROG042, + +17 October 2016 + +. + + + + +Paratypes +, +RMNH +Por. 11643, +Mauritius +, +Rodrigues +, +Mourouk Ebony +, +Castel Rock +, +19.76203°S +63.46273°E +, depth + +10 m + +, scuba, coll. +N.J. de Voogd +, field nr. ROG046, + +17 October 2016 + + +; + +RMNH +Por. 11645, +Mauritius +, +Rodrigues +, +Mourouk Ebony +, +Castel Rock +, +19.76203°S +63.46273°E +, depth + +10 m + +, scuba, coll. +N.J. de Voogd +, field nr. ROG048, + +17 October 2016 + + +. + + + +? +Additionally +: +ZMA +Por. 1 6368, +Madagascar +, +Nosy Bé +, +Ambariobé, N +of +Kosy Komba +, depth + +6–8 m + +, scuba, coll. +J.H. Stock +, + +28 December 1963 + +. + + + + + +Description. +The in situ shape is a massive lumpy sponge ( +Fig. 49a +) with irregular grooves and deep holes. Live color pale greyish white with pink rims in the peripheral parts. Surface irregular, in places somewhat conulose. Oscules inconspicuous, almost flush with the surface. Color of specimens on deck ( +Fig. 49b–c +) and preserved ( +Fig. 49d +) remains the same. Size of preserved specimens up to 13 x 8 + +x +8 + +cm, oscules +5 mm +in diameter. Grooves and ridges up to +1 cm +wide. Consistency coarse, harsh and hard. + + +Aquiferous system +. Leuconoid. + + +Skeleton. +A dense mass of giant triactines and small triactines. The oscules lead to into round atrial cavities lined with tetractines and triactines. + + +Spicules. +( +Figs 50a–d +) Giant triactines, small triactines, tetractines. + + +Giant triactines ( +Figs 50a +) equiradiate, equiangular, 408– +984 +–1380 +x 43 +– +107.2 +–204 µm. + + +Small triactines ( +Figs 50b +) equiradiate, equiangular, 124– +186 +–241 +x 10 +– +16.8 +–22 µm; small sagittal triactines with wavy paired actines (not shown), 83– +106 +–133 +x 7 +– +10.2 +–14 µm. + + +Tetractines ( +Figs 50c–d +) with basal triradiate system similar to triactines, 102– +163 +–204 +x 9 +– +12.6 +–16 µm, apical actines thin, curved ( +Fig. 50d +), 29– +58 +– +96 x 3 +– +5.2 +–8 µm. + + + + +Distribution and ecology. +Rodrigues +, possibly +Madagascar +, on reefs in shallow depth. + + + + +Etymology. +Sulcatus (L.) meaning grooved, referring to the habitus. + + + + +Remarks. +The spicule sizes and shapes are similar to those of + +Leucetta microraphis + +, to which the present species is most closely related. Two small irregular fragments of a white sponge, ZMA Por. 16368, collected near Nosy Bé, +Madagascar +, could belong to the present species based on its skeleton and spicules, but the small material without a definite shape precludes a definite conclusion. + + +We obtained sequences of the +holotype +and two of the +paratypes +and in our phylogenetic analysis ( +Fig. 2C +) they grouped together (at 85% bootstrap value) in a larger clade containing sequences of + +L. microraphis + +from + +Mayotte + +, +Madagascar +, +Australia +and the +Red Sea +. Aligned and trimmed sequences of this larger + +L. microraphis + +- group (length 396 sites), showing 19 non-conserved sites, resulted in observed differences of 2–8 sites between + +L. sulcata + + +sp.nov. + +and various sequences of + +L. microraphis + +s.l. +The four sequences of + +L. sulcata + + +sp.nov. + +shared two unique non-conserved sites. The three sequences of + +L. microraphis + +with pinkish red-brown-green color, described above from + +Mayotte + +and +Madagascar +, shared three unique non-conserved sites. These were not shared by the one Indonesian sequence of a specimen with similar morphology as the + +Mayotte + +and +Madagascar +specimens. + + +Remarkably, Oliver Voigt’s +Red Sea +sequences did not have any uniquely shared sites, individual sequences sharing non-conserved sites variously with + +L. sulcata + + +sp.nov. + +or +Western +Indian Ocean + +L. microraphis + +, and the Australian and Indonesian sequences. Clearly, the morphological discrepancies and inconsistencies in + +L. microraphis + +s.l. +are not easily solved by molecular sequence data. + +L. microraphis + +s.l. +are likely a complex of sister species. The morphological differences of the present new species (white color, grooved and holed habitus) with + +L. microraphis + +s.s. +(pinkish red-brown-green tubular masses) preclude conspecificity. The pink-white +Red Sea +specimens and + +L. pyriformis + +specimens described above are additional members of the group, differing in shape, color and e.g. in the long straight vs. curved condition of the apical actines of the tetractines. More study is necessary to differentiate the species. + + + +Leocorny +et al. +(2016) + +recently studied the + +Leucetta + +species from (sub-)tropical Australian waters: + +Leucetta prolifera +( +Carter, 1878 +) + +(originally as + +Teichonella + +), + +L. insignis +Row & Hozawa, 1931 + +, + +L. infrequens +Row & Hôzawa, 1931 + +, + +L. expansa +Row & Hôzawa, 1931 + +, + +L. villosa +Wörheide & Hooper, 1999 + +, + +L. foliata + +Leocorny +et al. +, 2016 + + +and + +L. purpurea + +Leocorny +et al. +, 2016 + + +. Of these species, two are slightly similar to the new species in having a folded habitus, + +L. prolifera + +and + +L. foliata + +, but the former has the folds broadly bladed with rows of oscules on the upper surface of the folds, whereas the latter has the folds sharply and thinly bladed. Both do not really resembly the irregularly grooved-holed specimens of the new species. Both species have next to the usual complement of giant triactines, small triactines and small tetractines also large tetractines of the same size or larger as the giant triactines. The remaining species have a more compact or globular habitus, also unlike our new species: + +L. insignis + +is shaped like + +L. chagosensis + +but has tripod-like giant triactines, + +L. infrequens + +is a small erect clump, which apparently lacks small tetractines, + +L. expansa + +is also a small, but squat clump, possessing ectosomal microdiactines in addition to the usual spicule complement, + +L. villosa + +is provided with villous hair-like outgrowths on the surface, and finally + +L. purpurea + +is a small globular purple-colored sponge with giant tripods, sharing this feature with + +L. insignis +. + + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC29A56FFF678C52FA9CFD69.xml b/data/38/6C/C6/386CC616DC29A56FFF678C52FA9CFD69.xml new file mode 100644 index 00000000000..132ebb57ed4 --- /dev/null +++ b/data/38/6C/C6/386CC616DC29A56FFF678C52FA9CFD69.xml @@ -0,0 +1,362 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Ute insulagemmae + +sp.nov. + + + + +Figs 54a–e +, +55a–g + + + + + +Material examined. +Holotype +, +ZMA +Por. 11562, +Seychelles +, + +Amirantes, +St. + +François Atoll, +Île Bijoutier +, reef, +7.0833°S +52.7333°E +, depth + +6–18 m + +, scuba, coll. +R.W.M. van Soest +, field nr + +. NIOP-E stat. 792/ +03, 5 January +1993. + + + + +Description. +Twin urn-shaped individuals ( +Fig. 54a +) joint at the base, with a narrow oscule each provided with a short naked collar. Color in life pale orange, in preservation shiny white. Length +1.3 cm +, diameter of an individual +5 mm +. Surface smooth. Consistency firm. + + +Aquiferous system +. Syconoid. + + +Skeleton. +( +Figs 54b–e +) A thin cortical skeleton of very small triactines ( +Figs 54b,d +) forming small meshes of 50–70 µm diameter covers a subcortical layer of lengthwise arranged giant diactines ( +Figs 54b–d +). This in turn overlies an articulated skeleton ( +Figs. 54c,e +) of larger triactines. Subatrial skeleton of tetractines and triactines, overlying the atrial skeleton ( +Fig. 54e +) of tetractines with their apical actines protruding in the atrial lumen. + + +Spicules. +( +Figs 55a–g +) Giant diactines, cortical small triactines, tubar triactines, (sub)atrial triactines, (sub-)atrial tetractines, trichoxeas. + + +Giant diactines ( +Fig. 55a +), fusiform, slightly curved or straight, equiended, 256– +1509 +– +2520 x 13 +– +68.1 +–116 µm. + + +Cortical triactines ( +Figs 55b +), sagittal, with strongly irregular paired actines and conical unpaired actines, occasionally reduced to conical tyle, unpaired actines 5– +9.4 +– +18 x 2 +– +4.1 +–6 µm, paired actines 21– +35 +– +51 x +2.5– +3.6 +–4 µm. + + +Tubar triactines ( +Figs 55c +), sagittal, but unpaired and paired actines usually not much different in lengths, paired actines straight or slightly curved, (overlapping in shape and size with subatrial triactines); possibly divisible in subcortical (larger) triactines and genuine (smaller) tubar triactines, but this was not readily visible; unpaired actines 52– +79.5 +–112 +x 8 +– +10.2 +–13 µm, paired actines 69– +85.1 +–117 +x 7 +– +8.8 +–13 µm. + + +Subatrial triactines ( +Fig. 55d +), strongly sagittal with unpaired actines distinctly longer than paired actines; unpaired actines 91– +168 +–203 +x 9 +– +12.4 +–15 µm, paired actines 78– +97 +–112 +x 9 +– +12.2 +–14 µm. + + + +FIGURE 54. + +Ute insulagemmae + + +sp.nov. + +, holotype ZMA Por. 11562, from Île Bijoutier, Seychelles, a, preserved habitus (scale bar = 1 cm), light microscopic image of surface skeleton, c, ditto of cross section of body wall, d, enlarged view of b, showing meshes made up of cortical triactines overlying subcortical giant diactines, e, enlarged view of c showing syconoid skeleton and protruding apical actines of atrial tetractines. + + + + +FIGURE 55. + +Ute insulagemmae + + +sp.nov. + +, holotype ZMA Por. 11562, SEM images of the spicules, a, diactines, b, cortical triactines, c, tubar triactines, d, subatrial triactines, e, subatrial tetractine, f, atrial tetractines, g, broken trichoxea from the short oscular collar. + + + +Subatrial tetractines ( +Fig. 55e +), recognizable by a long thinly tapering unpaired actine, which may occasionally have a distal swelling; unpaired actines 171–202–241 +x 8 +–10.2–11 µm, paired actines 76– +109 +–126 +x 10 +– +11.3 +–12 µm, apical actines curved 49– +60.4 +– +71 x 6 +– +7.1 +–8 µm. + + +Atrial tetractines ( +Figs 55f +), sagittal, with prominent curved apical actines; unpaired actines 61– +107.6 +–165 +x 7 +–8.6–11 µm, paired actines 68– +104 +–126 +x 6 +– +8.3 +–10 µm, apical actines 40– +115 +–201 +x 6 +– +8.4 +–11 µm. + + +Trichoxeas ( + +Fig. +55g + +), from the short oscular collar, invariably broken, fragments measure 180–650 +x 2 +µm. + + + + +Distribution and ecology. +Known only from the +type +locality on the outer reef of Île Bijoutier, at +6–18 m +depth. + + + + +Etymology. +The name is a noun composed of insula (L.) = island, gemma (L.) = jewelry, referring to the +type +locality Île Bijoutier (‘jewelry island’). + + + + +Remarks. +Wörheide & Hooper (2003) +described + +Ute ampullacea + +from the Great Barrier Reef, NE +Australia +. This has similar habitus and spiculation, but the cortical skeleton consists of microdiactines, whereas in the new species these are replaced by irregular small triactines ( +Fig. 55b +). We obtained molecular data for the new species and compared these with GenBank sequences of + +Ute + +and + +Synute + +. Remarkably, in our Calcaronea phylogeny ( +Fig. 3 +) + +Ute ampullacea + +and our new species do not show close relationship, as the former ended up in a group of +Lelapiidae +. The nearest species to + +Ute insulagemmae + + +sp.nov +. + +appear to be Australian + +Ute + +aff. +syconoides +( +Carter, 1886 +) and Australian + +Synute pulchella +( +Dendy, 1892 +) + +, which grouped in a well-supported clade (86% bootstrap value) with our new species. Separate inspection of a trimmed alignment of 404 sites of these three species, showed 19 non-conserved sites indicating that the species are probably not closely related. +No +other + +Ute + +species have been reported from the tropical Indo-West Pacific. + + +The + +Ute + +group appeared in our Calcaronea phylogeby ( +Fig. 3 +) in the midst of a group of +Heteropiidae +and +Jenkinidae +. We interprete this result as evidence of insufficient taxon support for our Calcaronea phylogeny. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC2AA56AFF678D74FABDFC51.xml b/data/38/6C/C6/386CC616DC2AA56AFF678D74FABDFC51.xml new file mode 100644 index 00000000000..ab178ff1708 --- /dev/null +++ b/data/38/6C/C6/386CC616DC2AA56AFF678D74FABDFC51.xml @@ -0,0 +1,326 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Grantia +aff. +indica +Dendy, 1913 + + + + + +Figs. 52a–e +, +53a–f + + + + +? + +Grantia indica +Dendy, 1913: 20 + +, pl. 2 fig. 3, pl. 4 figs 4–5. + + + + +Material examined. +ZMA +Por. 10223b, +Seychelles +, +Mahé +, NE coast, Cap Maçons and Anse de Forbans, +4.7667°S +55.5167°E +, depth +0–6 m +, snorkeling, coll. R.W.M. van Soest, field nr. +NIOP-E +stat. 612, +12 December 1992 +; +ZMA +Por. 11566b, +Seychelles +, Amirantes, Île Desnoeufs platform, outer slope, +6.2167°S +53.0167°E +, depth +12–15 m +, scuba, coll. R.W.M. van Soest, field nr. +NIOP-E +stat. 738/22, +2 January 1993 +; +ZMA +Por. 11749, +Seychelles +, Amirantes, Île Desnoeufs platform, outer slope, +6.2167°S +53.0167°E +, depth +12–15 m +, scuba, coll. R.W.M. van Soest, field nr. +NIOP-E +stat. 738/24, +2 January 1993 +. + + + + +Description. +Small white, very ‘hairy’, sycon-like individuals ( +Fig. 52a +). Largest specimen squat, +5 mm +high, +4 mm +in diameter, but smaller specimens ( +Figs. 52b–c +) may be more elongate. Fringe of long diactines ( +Figs 52b, d +) about +1 mm +long. + + +Aquiferous system +. Syconoid. + + +Skeleton. +( +Figs 52d–e +) Skeleton articulate, with long diactines protruding obliquely from the surface, cortical skeleton a layer of larger and smaller sagittal triactines, tubar skeleton consists of rows of triactines. Subatrial skeleton of sagittal tetractines, atrial skeleton of tetractines with long apical actines, protruding into the atrial lumen ( +Fig. 52e +). Fringe consists of long diactines supported by sagittal tetractines ( +Fig. 52d +). + + +Spicules. +( +Figs. 53a–f +) Diactines, trichoxeas, sagittal triactines, and sagittal tetractines. + + +Diactines of the main body ( +Fig. 53a +), inequiended, blunt at the proximal end, sharp at the distal end, quite variable in length both in the same specimen and among specimens, 276– +641 +– +1022 x 10 +– +19.4 +–24 µm. + + + +FIGURE 52. + +Grantia +aff. +indica +Dendy, 1913 + +, ZMA Por. 11556b, from the Seychelles, a, three individuals (scale bar = 1 cm), b, light microscopic image of small individual, c, detail of the same, d, light microscopic image of the fringe of trichoxeas supported by tetractines, e, cross section of body wall and atrium, showing syconoid structure and apical actines of atrial tetractines protruding in the atrial lumen. + + + + +FIGURE 53. + +Grantia +aff. +indica +Dendy, 1913 + +, ZMA Por. 11556b, SEM images of the spicules, a, diactines of the cortical skeleton, b, broken fragment of trichoxea from the fringe, c, cortical triactine, d, tubar triactines, e, subatrial tetractines, f, atrial tetractines. + + + +Trichoxeas ( +Fig. 53b +) of the fringe, inequiended with one end slight swollen and the other sharply pointed, often broken, length of the larger fragments 420–970–2000 µm, thickness 1.5– +4.1 +–8 µm. + + +Cortical triactines ( +Fig. 53c +), sagittal with oxhorn-shaped paired actines; unpaired actines 33– +108 +–165 +x 4 +– +6.7 +–12 µm, paired actines 66– +80 +– +99 x 4 +– +5.9 +–7 µm. + + +Tubar triactines ( +Figs 53d +), sagittal, with straight or slightly curved paired actines, occasionally T-shaped; length of unpaired actines 45– +73 +–120 +x 6 +– +9.4 +–13 µm, paired actines 66– +102 +–156 +x 7 +– +9.7 +–12 µm; these also occur in a low number in the fringe. + + +Subatrial and fringe tetractines ( +Figs 53e +), unpaired actine usually longer than paired actine, with short apical actine; unpaired actines 78– +114 +–156 +x 7 +– +8.4 +–11 µm, paired actines 48– +90.0 +–104 +x 7 +– +7.7 +–9 µm, apical actines 14– +23 +– +39 x 3 +– +4.7 +–7 µm. They occur also in the fringe. + + +Atrial tetractines ( +Figs 53f +), with straight unpaired actines, almost straight paired actines and long slightly curved apical actines; unpaired actines 105– +139 +–174 +x 8 +– +8.3 +–10 µm, paired actines 90– +132 +–171 +x 6 +–7.2–8 µm, apical actines 54– +128 +–210 +x 5 +–7.8–9 µm. + + + + +Distribution and ecology. +Seychelles +, shallow reef down to + +15 m +. + + + + + +Remarks. +The present material shares the shape and the composition of the spicule package with Dendy’s (1913) +type +, but almost all spicules are smaller and thinner. Dendy is known to frequently cite only the largest measurements for a spicule category. The +type +was larger ( +10 x +4.8 mm +) than our specimens and that may be an additional cause of the spicule size differences, but it is also possible that our material belongs to a closely related separate species, hence our ‘aff.’ designation. For the time being we emphasize the shared characters. + +Unfortunately, our attempt to obtain 28S rRNA sequences failed. + + + + +Sycon tabulatum +( +Schuffner, 1877 +) + +(originally as + +Sycandra + +) has similar shape, but the radial tubes are crowned by a conus of small diactines and there are no giant diactines. The original combination is preoccupied by + +Sycandra tabulata +Hackel, 1872 + +. Below (section ‘Additional species..’), a new name for Schuffner’s species is proposed. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC2CA56EFF678B80FC65FDA4.xml b/data/38/6C/C6/386CC616DC2CA56EFF678B80FC65FDA4.xml new file mode 100644 index 00000000000..a5157164d13 --- /dev/null +++ b/data/38/6C/C6/386CC616DC2CA56EFF678B80FC65FDA4.xml @@ -0,0 +1,380 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucandra pulvinar +( +Haeckel, 1872 +) + + + + + +Figs 56a–d +, +57a–e + + + + + +Sycolepis pulvinar +Haeckel, 1870: 251 + +( +nomen nudum +) + + + + +Mlea dohrnii +Miklucho-Maclay + +MS in + +Haeckel, 1872 +: 162 + +( +nomen nudum +) + + + + + +Leucortis pulvinar +var. +semitica + +Haeckel, 1872 +: 163 + + + + + + + +Leucandra pulvinar + +; + +Dendy 1905 +: 234 + +(listed, not described) + + + + + + + +Material +examined. + +ZMA +Por. 13423, +Israel +, +Stylus Pinnacle +, +Gulf +of Aqaba, depth + +9 m + +, scuba, coll. +M. Wunsch +, field nr. AQ + +77, 6 July + +1998 + +; + +ZMA +Por. 13615, +Israel +, NW of harbor, +Gulf +of Aqaba, under overhang on harbor pile, depth + +12 m + +, scuba, coll. +M. Wunsch +, field nr. AQ + +39, 3 July + +1998. + + + + + +Description. +Whitish or pale yellow globular-lobate sponges ( +Figs 56a,d +) with optically smooth or irregular hispid surface, approximately 3 +x 2 +x +1.5 cm +. Both specimens have two prominent oscules, +3–4 mm +in diameter, with naked collar, leading to atrial spaces that are shallow and narrow. In preserved condition the color is beigedirty white ( +Fig. 56b +). Consistency brittle, firm. + + +Aquiferous system +. Leuconoid. + + +Skeleton +( +Fig. 56c +). A thin cortical skeleton of sagittal triactines covering tangential giant diactines arranged in all directions. There are also tangential trichoxeas. Choanosomal skeleton a confused mass of irregular triactines with scattered diactines of all sizes. Atrial skeleton consists of small irregular triactines. + + + +Spicules +( +Figs 57a–e +). Diactines, trichoxeas, sagittal triactines, irregular triactines. +No +tetractines. + + + +Diactines fusiform ( +Figs 57a,a +1 +), varying in size from giant to very small, 105– +929 +– +2760 x 11 +– +47 +–108 µm. + + +Trichoxeas ( +Figs 57b,b +1 +), often broken, but also varying in length, 123– +465 +– +1200 x +1.5– +3.4 +–7 µm. + + +Cortical triactines ( +Fig. 57c +), predominantly sagittal, almost T-shaped, with unpaired actine shorter than paired actines, although equiactinal spicules also occur, unpaired actines 90– +143 +–212 +x 9 +– +14.7 +–20 µm, paired actines 165– +198 +–270 +x 14 +– +16.3 +–21 µm. + + +Choanosomal triactines ( +Fig. 57d +), basically equiactinal, but irregularly sagittal or oxhorns-haped, 168– +229 +–298 +x 15 +– +19.1 +–24 µm. + + +Atrial triactines ( +Fig. 62e +), smaller than the other triactines, equiactinal, irregularly parasagittal, 45– +91 +–120 +x 5 +– +8.1 +–10 µm. + + + + +Distribution and ecology. +Red Sea +, + +Sri +Lanka + +, shallow reef localities. + + + + +Remarks. +Our specimens resemble Haeckel’s 1872 description (vol. 2: 163) and figures (vol. 3: pl. 29 figs 1–10) of + +Leucortis pulvinar +var. +semitica + +. Next to this variety, Haeckel also described a + +var. +indica + +. Since he did not describe a typical, separate variety one of the two varieties ( + +semitica + +or + +indica + +) has to be the nominotypical variety (ICZN art. 47) + +Leucortis pulvinar +var. +pulvinar + +. In the absence of previous treatments of this problem, we choose here the + +var. +semitica + +as the nominotypical variety to take the name + +pulvinar + +, as it is the first mentioned. It is likely that both varieties belong to the same species, but a formal synonymization must await the description of recent Indian material. Dendy’s (1905) + +Sri +Lanka + +record of + +Leucandra (Leucortis) pulvinar + +remains undescribed. + + +There are several + +Leucandra + +species described in the region with similar spiculation, including giant diactines: + +Leucandra echinata +Schuffner, 1877 + +(also reported by Dendy 1913), + +Leucandra fascigera +Schuffner, 1877 + +, + +Leucandra donnani +var. +tenuiradiata +Dendy, 1916 + +, + +Leucandra dwarkaensis +Dendy, 1916 + +and + +Leucandra seychellensis +Hozawa, 1940 + +), but all these have atrial tetractines and differ in habitus. This also applies to two + +Leucandra + +species from NE +Australia +, + +L. sphaeracella +Wörheide & Hooper, 2003 + +, and + +L. nicolae +Wörheide & Hooper, 2003 + +. + +Unfortunately, our attempt to obtain a partial 28S sequence failed. + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC2DA552FF678EC5FAE2FCC4.xml b/data/38/6C/C6/386CC616DC2DA552FF678EC5FAE2FCC4.xml new file mode 100644 index 00000000000..ed6534ad3aa --- /dev/null +++ b/data/38/6C/C6/386CC616DC2DA552FF678EC5FAE2FCC4.xml @@ -0,0 +1,382 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucandra pilula + +sp.nov. + + + + +Figs 58a–g +, +59a–e + + + + + + +Material +examined. + +Holotype +, +ZMA +Por. 10528, +Seychelles +, +Bird Island +, +3.7167°S +55.2167°E +, coastal reef at + +13 m + +depth, scuba, coll. +W. Kolvoort +, field nr. +NIOP-E +stat. 717/34, + +20 December 1992 + + +. + + +Paratypes +, +ZMA +Por. 10379a, +Seychelles +, +Mahé +, E coast, N of Moyenne Island, +4.6167°S +55.5167°E +, depth +1–7 m +, reef, snorkeling, coll. R.W.M. van Soest, field nr. +NIOP-E +stat. 606, +10 December 1992 +; +ZMA +Por. 10641 ( +2 specimens +), +Seychelles +, Amirantes, St. François Atoll, Île Bijoutier, depth +3 m +, reef, scuba, coll. R.W.M. van Soest, field nr. +NIOP-E +stat. 792/21, +6 January 1993 +; +ZMA +Por. 11564, +Seychelles +, Amirantes, N of Platte Island Atoll, +5.8167°S +55.3667°E +, depth +6 m +, reef, coll. R.W.M. van Soest, field nr. +NIOP-E +stat. stat. 796/42, +7 January 1993 +. + + + + +Description. +Small white or beige-white globules ( +Figs 58a–d +), with a single apical oscule, flush with the surface, which is optically smooth but feels rough. Size of body up to +1.5 cm +high, +1 cm +in diameter; oscule +2–3 mm +in diameter. In preservation they stay white. Consistency firm. + + + +FIGURE 57. + +Leucandra pulvinar +(Haeckel, 1872) + +, ZMA Por. 13423, from Gulf of Aqaba, Red Sea, SEM images of spicules, a, giant diactines, a1, detail of sharp end of giant diactine, b, trichoxea, b1, detail of same, c, cortical triactine, d, choanosomal triactine, e, atrial triactine. + + + +Aquiferous system +. Leuconoid. + + +Skeleton. +( +Figs 58e–g +) Cortical skeleton ( +Fig. 58f +) of intermediate sized triactines overlying a mass ( +Fig. 58e +) of giant and smaller triactines forming the choanosomal skeleton supporting the leuconoid aquiferous canal system. The atrial skeleton ( + +Fig. +58g + +) consists of sagittal triactines and tetractines, the latter with apical actines protruding into the atrial lumen. The oscular rim is supported by trichoxeas. + + +Spicules. +( +Figs 59a–e +) Giant triactines, oxhorn-shaped triactines, small triactines, tetractines, trichoxeas. + + +Giant triactines ( +Figs 59a +) of the main body wall, actines straight, tapering gradually to sharp points, equiangular and equiradiate or more often sagittal or with all actines of different lengths, 312– +628 +–985 +x 19 +– +55.7 +–93 µm. + + + +FIGURE 58. + +Leucandra pilula + + +sp.nov. + +, from the Seychelles, a–d, preserved habitus of holotype ZMA Por. 10528 (c) and paratypes ZMA Por. 10379, 11564 and 10641 (a,b and d), e–g, SEM images of the skeleton, e, cross section, f, view of surface skeleton, g, view of atrial skeleton. + + + +Oxhorn triactines ( +Figs 59b +) of the cortical skeleton, sagittal with curved paired actines and straight unpaired actines, unpaired actines 178– +245 +–326 +x 15 +– +22.7 +–31 µm, paired actines 216– +281 +–372 +x 16 +– +21.6 +–28 µm. + + +Small triactines ( +Figs 59c +) of the main body and the subatrial region, sometimes equiradiate equiangular but more often irregularly sagittal, or T-shaped, unpaired actines 94– +172 +–254 +x 9 +– +17.8 +–26 µm, paired actines 100– +186 +–303 +x 11 +– +16.6 +–29 µm. + + +Tetractines ( +Figs 59d +) of the atrial skeleton, sagittal, usually with unpaired actine shorter than paired actines, which are usually straight, occasionally slightly curved, unpaired actines 101– +186 +–271 +x 14 +– +19.4 +–32 µm, paired actines 136– +239 +–380 +x 9 +– +17.1 +–32 µm, apical actines slightly curved, 45– +84 +–130 +x 4 +– +8.4 +–11 µm. + + +Trichoxeas ( +Fig. 59e +) of the oscular region, not common, almost invariably broken, 100–300 +x 1–2 +µm. + + + + +FIGURE 59 +. + +Leucandra pilula + + +sp.nov. + +, SEM images of the spicules, a, giant triactines of the choanosome, b, cortical triactines, c, small triactines of the choanosome and subatrial region, d, tetractines of the atrial skeleton, e, fragment of trichoxea from the oscular rim. + + + + +Distribution and ecology. +Seychelles +only, but widespread throughout the archipelagoes, on reefs, depths + +1– +13 m + +. + + + + +Etymology. +Pilula (L.) = small ball, a noun referring to the habitus. + + + + +Remarks. +The size of all specimens is uniformly +1–1.5 cm +high and +1 cm +in diameter, and thus it is likely that this feature is characteristic for the species. The shapes of the triactines and tetractines are somewhat variable among the +5 specimens +obtained of this species, but invariably there are giant triactines, smaller cortical triactines and smaller subatrial triactines. The atrial tetractines vary in the length of the paired actines, within and among specimens. However, the overall spicule package is similar in all and the lack of giant diactines is shared by all. + + +Similar-sized specimens were described by +Jenkin (1908) +from Zanzibar under the name + +Leucandra ananas +( +Haeckel, 1872 +) + +, a species from the Northern Atlantic. This differs cleary by having tufts of large diactines of up to 3000 µm in length projecting from the surface. It is likely an undescribed species. + + +By the lack of diactines this species stands out among all known + +Leucandra + +species of the Western Indian Ocean region (but see below). There are no matching descriptions in the region. + + +We obtained a 28S sequence of the +holotype +of our new species and compared these to the sequences from GenBank of + +Leucandra nicolae +Wörheide & Hooper, 2003 + +and a new species, + +L. mozambiquensis + + +sp.nov. + +described below. There are no other partial 28SrRNA sequences of + +Leucandra + +available from the region and moreover the genus has been shown to be non-monophyletic ( + +Dohrmann +et al. +2006 + +). In our Calcaronea phylogeny ( +Fig. 3 +) the three species grouped in a shared clade with modest bootstrap value (52%), with + +L. pilula + + +sp.nov. + +and + +L. nicolae + +closer (bootstrap value 65 %). A separate inspection of the trimmed alignment of these three species (length 431 sites) showed 15 non-conserved sites, indicating the species are probably not closely related. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC33A574FF678F06FB5CFA04.xml b/data/38/6C/C6/386CC616DC33A574FF678F06FB5CFA04.xml new file mode 100644 index 00000000000..7560536b99e --- /dev/null +++ b/data/38/6C/C6/386CC616DC33A574FF678F06FB5CFA04.xml @@ -0,0 +1,458 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucaltis nodusgordii +( +Poléjaeff, 1883 +) + + + + + +Figures 37a–e +, +38a–f +. + + + + + +Heteropegma nodusgordii +Poléjaeff, 1883 + +(in part, only the Torres Strait material): 45, pl. I fig. 7, pl. IV figs 1a–d. + + + + +Leucaltis clathria + +; Dendy 1913: 16, pl. 1 figs 1–2; + +Hôzawa 1940 +: 136 + +, pl. VI fig. 3; + +Wörheide & Hooper 1999 +: 876 + +, figs +7I +–S (not: +Haeckel 1872 +). + + + + +Leucaltis nodusgordii + +; Van Soest & De Voogd 2015: 39, figs 28a–c, 29a–d, 30a–e (with further synonyms). + + + + +FIGURE 36. +Ernstia +spec., RMNH Por. 10161c, from the Maldives, a, habitus in situ (arrow), b, light microscopic overview of the cormus, c–e, SEM images of the spicules, c, triactines, d, tetractine, e, detail of apical actine of tetractine. + + + + +Material examined. +ZMA +Por. 12436, +Seychelles +, Amirantes, Desroches Atoll, SW rim, outer reef slope, +5.7167°S +53.6167°E +, depth +5–30 m +, scuba, coll. M.J. de Kluijver, field nr. +NIOP-E +stat. 774/03, +30 December 1992 +; +ZMA +Por. 12443, +Seychelles +, Amirantes, Poivre Atoll, N rim, outer reef slope, +5.7333°S +53.3167°E +, depth +7–8 m +, scuba, coll. R.W.M. van Soest, field nr. +NIOP-E +stat. 768/08, +31 December 1992 +; +ZMA +Por. 16248, +Seychelles +, +Mahé +, SE coast, +Anse Royale +Bay, +4.7333°S +55.5167°E +, depth +2–13 m +, scuba, coll. R.W.M. van Soest, field nr. +NIOP-E +stat. 740/04, +24 December 1992 +; +ZMA +Por. 20623, +Seychelles +, +Mahé +, NE Point, +4.5833°S +55.4667°E +, depth +0–5 m +, snorkling, coll. R.W.M. van Soest, field nr. +NIOP-E +stat. 604, +8 December 1992 +. + + + + +Description. +Because this species has been treated recently in Van Soest & De Voogd (2015), we refrain from extensively describing the +Seychelles +material. The species forms masses of loosely anastomosed tubes ( +Fig. 37a +), size up to +3 x +4 cm +, individual tubes approximately +0.5 cm +in diameter. Color pale blue or bluish white in situ, white in preservation. Some of the tubes have open endings, presumably oscules. Consistency fragile, surface optically smooth, but feels rough. + + +Aquiferous system. +Elongate, ramified choanocyte chambers, supported by small equiangular spicules. + + +Skeleton. +( +Figs 37–e +) In cross section ( +Fig. 37b +) from outside to atrium, there is a cortical skeleton of giant tri- and tetractines ( +Fig. 37c +), a choanosomal skeleton ( +Fig. 37d +) of small thin equiangular and equiradiate tri- and tetractines, and an atrial membrane ( +Fig. 37e +) supported by small sagittal (‘abruptly’-angled) tri- and tetractines. + + + +FIGURE 37. + +Leucaltis nodusgordii +(Poléjaeff, 1883) + +, ZMA Por. 16248, from the Seychelles, a, preserved habitus (scale bar = 1 cm), b–e, SEM images of the skeleton, b, cross section of tube, c, surface of the tube showing cortex of giant tri- and tetractines, d, part of the choanosomal skeleton showing small regular tri- and tetractines, e, atrial skeleton of sagittal ‘abruptly’ angled tri- and tetractines. + + + + +FIGURE 38. + +Leucaltis nodusgordii +(Poléjaeff, 1883) + +, ZMA Por. 16248, from the Seychelles, a–f, SEM images of the spicules, a, cortical giant tetractines, b, cortical giant triactines, c, choanosomal regular tetractine, d, choanosomal regular triactine, e, atrial sagittal ‘abruptly’ angled tetractine, f, atrial sagittal ‘abruptly’ angled triactine. + + + +Spicules. +( +Figs 38a–f +) Giant tri- and tetractines, small regular tri- and tetractines, small sagittal tri- and tetractines. + + +Giant tetractines ( +Figs 38a +), quite variable in size, similar in shape and size to the giant triactines, actines 144– +571 +– +1020 x 18 +– +79.8 +–126 µm. + + +Giant triactines ( +Figs 38b +), quite variable in size, equiangular and equiradiate, with thick conical actines measuring 102– +505 +–960 +x 14 +– +60.2 +–138 µm. + + +Regular equiangular equiradiate tetractines ( +Fig. 38c +), with thin cylindrical actines; basal radiate actines 60– +73 +– +84 x 2 +– +2.4 +–4 µm, with apical actines 9– +20.7 +– +28 x 2 +– +2.1 +–3 µm. + + +Regular equiangular equiradiate triactines ( +Fig. 38d +), with thin cylindrical actines measuring 59– +66.9 +– +78 x 2 +– +2.1 +–3 µm. + + +Sagittal, abruptly angled tetractines ( +Fig. 38e +), with unpaired actines 39– +57 +– +69 x +2.5– +3.5 +–5 µm, paired actines 60– +69 +– +84 x 2 +– +3.4 +–5 µm, apical actines 18– +29.8 +– +45 x 2 +– +2.9 +–5 µm. + + +Sagittal, abruptly angled triactines ( +Fig. 38f +), similar to the sagittal tetractines, with unpaired actines 36– +50 +– +63 x 2 +– +2.8 +–4.5 µm, paired actines 54– +64 +– +81 x 2 +– +3.1 +–4.5 µm. + + + + +Distribution and ecology. +Seychelles +, +Cargados Carajos +, +Australia +, + +Sri +Lanka + +, +Indonesia +, on reefs at depths down to + +88 m +. + + + + + +Remarks. +The data for the +Seychelles +specimens closely conform to those of the Indonesian material described by us recently. Size of the +Seychelles +specimens is smaller than the Indonesian ones, but individual tubes are similar in both. The giant tetractines of the Indonesian specimens were reported as somewhat larger. Unfortunately, Dendy’s (1905) record of this species from + +Sri +Lanka + +was not described, so we do not know whether this inbetween locality had inbetween sizes. + + +We obtained sequences of an Indonesian specimen described in our 2015 paper (RMNH Por. 1772) and two of the +Seychelles +specimen (ZMA Por. 12436 and 12443) treated here. We also downloaded longer 28S sequences from GenBank of a Panamanian (Caribbean) + +Leucaltis + +sp. = + +L. clathria +( +Haeckel, 1872 +) + +, proclaimed a different species by us (Van Soest & De Voogd, 2015; Van +Soest, 2017 +), and two Australian sequences named + +L. clathria +( +Haeckel, 1872 +) + +(acc.nrs. +JQ272302 +and +AY563542 +), which are assumed to be conspecific with Indonesian and +Seychelles +specimens of + +L. nodusgordii + +. As the detailed relationships between these specimens are not clearly apparent in +Fig. 2B +, we did a separate analysis of the aligned and trimmed sequences of these six specimens (alignment length 369 sites), which showed 21 non-conserved sites. Where the maximum site difference between the five sequences from the Indo-West Pacific was 6 or less, the Panamanian sequence had 11 unique nonconserved sites, along with two non-conserved sites shared with +Indonesia +and one with +Australia +. This supports the previously claimed separate specific status of the Caribbean + +Leucaltis + +populations, even though the differences among the specimens are not significant enough to show up in the phylogenetic analysis of our +Fig. 2B. + + +A possible junior synonym of + +Leucaltis nodusgordii + +is + +Leucaltis bathybia +var. +mascarenica +Ridley, 1884 + +, reported from the Amirantes, very near to two of our collected specimens (ZMA Por. 12436 and 12443). Ridley’s description of the habit and the large tetractines sounds close to our material, but there is not sufficient information to be certain. + +Leucaltis bathybia +Haeckel, 1872 + +from +600 m +depth in the +Red Sea +is not conspecific judging from its description (see also below). It is assigned to + +Leucandra + +at present (see Van + +Soest +et al. +2018 + +), but the predominance of large tetractines makes it more likely that it belongs to + +Leucilla + +. + +L. bathybia + +was associated with + +Sycettusa + +(Calcaronea, +Heteropiidae +) by +Burton (1963, p. 318) +but this cannot be accepted. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC37A579FF678E3CFF25FE11.xml b/data/38/6C/C6/386CC616DC37A579FF678E3CFF25FE11.xml new file mode 100644 index 00000000000..92bc4eabf0a --- /dev/null +++ b/data/38/6C/C6/386CC616DC37A579FF678E3CFF25FE11.xml @@ -0,0 +1,317 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leuclathrina translucida + +Voigt +et al. +, 2018 + + + + + + +Figures 39a–f +, +40a–c + + + + + + +Leuclathrina translucida + + +Voigt +et al. +, 2018 + +: 151 + + +, figs 2A–I, 3A–F. + + + + + + + +Material +examined. + +RMNH +Por. 10072, +Maldives +, +Faafu Atoll +, +Wallino +, +3.087472°N +72.9567°E +, depth + +20 m + +, scuba, coll. +N.J. de Voogd +, field nr. +MAD02 +/MAS022, + +16 February 2015 + + +; + +RMNH +Por. 10090, +Maldives +, +Faafu Atoll +, +Coral Garden +, +3.0875°N +72.968861°E +, depth + +18 m + +, scuba, coll. +N.J. de Voogd +, field nr. +MAD04 +/MAS043, + +17 February 2015 + + +. + + + + +Description. +In life, these sponges form pale yellow cushions ( +Figs 39a–b, e +) consisting of dense layers of anastomosed thin tubes, from which issue long upright tubes. These long tubes are yellow at the base, but become transparent towards their ends ( +Figs 39a–b +). The ends may be broadly flattened or occasionally bifid or curling downwards. The tubes are mostly closed but some are open and may function as oscules. The yellow base is ‘punctate’, i.e. there are regularly spaced rounded openings separating the tubes. On deck photos ( +Figs 39c,f +) show the specimens to become uniformly yellow, while preserved specimens ( +3 in +RMNH 1 0 0 72, 1 in RMNH 10090) become pale orange-brown all over ( +Fig. 39d +). The size of preserved specimens is up to 4 + +x 3 x +1 + +cm, length of upright tubes +1–2 cm +, width +3–4 mm +, but the preservation has caused notable shrinkage, so in situ sizes are larger. + + +Aquiferous system. +Leuconoid, not supported by spicules. + + + +FIGURE 39. + +Leuclathrina translucida +Voigt +et al. +, 2018 + +, RMNH Por. 10072 and 10090 from the Maldives, habitus in situ, on deck and preserved, a–b, habitus in situ of RMNH Por. 10072, c, habitus on deck of RMNH Por. 10072 (both photos N.J. de Voogd), d, preserved habitus of RMNH Por. 10072 (scale bar = 1 cm), e, habitus in situ of RMNH Por. 10090, f, habitus on deck of RMNH Por. 10090 (both photos N.J. de Voogd). + + + +Skeleton. +( +Figs 40a,b +) Thickness of tube walls consisting of two layers of overlapping triactines, or more than two layers in the upright long tubes. Insides of the bottom layer tubes and the basal parts of the long upright tubes ( +Fig. 40b +) covered in yellow-colored organic mass, devoid of spicules, presumed to be choanoderm. The extent and thickness of this choanoderm precludes the tubes to be asconoid. This organic layer is absent from the end of the long tubes coinciding with the transparent parts observed in situ. + + +Spicules. +( +Figs 40c +) Triactines only. + + + +FIGURE 40. + +Leuclathrina translucida +Voigt +et al. +, 2018 + +, RMNH Por. 10072, from the Maldives, a, light microscopic image of surface skeleton, b, light microscopic image of a longitudinal cross section of a tube, showing surface cover of spicules and choanosomal soft parts, c, SEM images of the spicules. + + + +Triactines, equiradiate and equiangular, in a large size range, 101– +181 +–243 +x 8 +– +13.1 +–19 µm (RMNH Por. 10072: 101–238 +x 8–19 +µm, RMNH Por. 10090: 122–243 +x 10–15 +µm). + + + + +Distribution and ecology. +Maldives +, coral reefs + + + + +Remarks. +This is a peculiar and deviating +Clathrinida +, assigned to + +Leuclathrina + +by + +Voigt +et al. +(2018) + +because of the presence of uniformly sized triactines at the surface with a choanoderm not supported by spicules. The 28S sequence we obtained (GenBank acc.nr. +MF872789 +) grouped with Oliver Voigt’s sequence (nr. GW393) with 99% bootstrap value confirming the specimens belong to the same species. Because the affiliation of this species is rather uncertain, we included in our phylogenetic tree several sequences of possible close relatives ( + +Burtonulla +, +Ascandra +, +Levinella + +and + +Soleneiscus +) + +. Although + +Leuclathrina translucida + +appeared indeed in the same clade as these genera (cf. +Fig. 2B +), the bootstrap value is low, so none of the mentioned genera is likely close. + + +In the process, we made the discovery that the Indonesian +Ernstia chrysops +Van Soest & De Voogd, 2015 is apparently not an +Ernstia +but more likely an + +Ascandra + +. + + +So far, the position of + +Leuclathrina translucida + +in the molecular tree of +Fig. 2 +is outside and independent of the clades of + +Clathrina + +, + +Leucaltis, Ernstia + +and + +Leucetta + +. + +Ascandra + +species may have a rather similar habitus, but they have a majority and diversity of tetractines. Previously, + +Leuclathrina + +was monospecific and occurred in bathyal coral reefs off the coasts of +Northwestern +Europe. This second species is unlike the +type +species in shape, color and habitat. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC39A57DFF678C37FCE3F844.xml b/data/38/6C/C6/386CC616DC39A57DFF678C37FCE3F844.xml new file mode 100644 index 00000000000..3d1423956f4 --- /dev/null +++ b/data/38/6C/C6/386CC616DC39A57DFF678C37FCE3F844.xml @@ -0,0 +1,515 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucetta chagosensis +Dendy, 1913 + + + + + +Figs 43a–f +, +44a–g + + + + + +Leucetta chagosensis +Dendy, 1913: 10 + +, pl. 1 fig. 6, pl. 4 fig. 2; Van Soest & De Voogd 2015: 51, figs 37a–f, 38a–d, with further synonyms. + + + + +Ascoleucetta sagittata + + +Cavalcanti +et al. +, 2013 + +: 308 + + +, figs 21–22; Van Soest & De Voogd 2015: 49, figs 36a–f. + + + + + +Material examined. +RMNH +Por. 9171, +Saudi Arabia +, Al Laith, Quita al Qursh (Shark Reef), +20.1327°N +40.0994°E +, depth +7.8–9.1 m +, scuba, coll. Diaa Youssef, field nr. KSA-51, +14 May 2013 +; +RMNH +Por. 9621, +Saudi Arabia +, Jeddah, near Thuwal, Al Asoul, +22.265361°N +39.002139°E +, coll. N.J. de Voogd, scuba, field nr. THU07/ JED116, +9 November 2014 +; +RMNH +Por. 9637, +Saudi Arabia +, Jeddah, near Thuwal, Um Alsawi, +22.239306°N +38.985139°E +, coll. N.J. de Voogd, scuba, field nr. THU08/JED137, +11 November 2014 +; +RMNH +Por. 9638, +Saudi Arabia +, Jeddah, near Thuwal, Um Alsawi, +22.239306°N +38.985139°E +, coll. N.J. de Voogd, scuba, field nr. JED138, +11 November 2014 +; +RMNH +Por. 9676, +Saudi Arabia +, Jeddah, near Thuwal, Fsar, +22.229611°N +39.029028°E +, scuba, coll. N.J. de Voogd, field nr. THU12/JED181, +13 November 2014 +; +RMNH +Por. 10073, +Maldives +, Faafu Atoll, Wallino, +3.087472°N +72.9567°E +, depth +15 m +, scuba, coll. N.J. de Voogd, field nr. +MAD +02/MAS023, +16 February 2015 +; +RMNH +Por. 10114, +Maldives +, Faafu Atoll, Route 66, +3.07825°N +72.976306°E +, depth +20 m +, scuba, coll. N.J. de Voogd, field nr. +MAD +09/MAS069, +20 February 2015 +; +RMNH +Por. 10141, +Maldives +, Faafu Atoll, Sunny Reef, +3.144639°N +73.012667°E +, depth +7 m +, scuba, coll. N.J. de Voogd, field nr. +MAD +08/MAS099, +18 February 2015 +; +RMNH +Por. 10144, +Maldives +, Faafu Atoll, Route 66, +3.07825°N +72.976306°E +, depth +20 m +, scuba, coll. N.J. de Voogd, field nr. +MAD +09/MAS105, +20 February 2015 +; +RMNH +Por. 11601, +Mauritius +, +Rodrigues +, La Rampe, +19.65015°S +63,41323333°E +, depth +18 m +, scuba, coll. N.J. de Voogd, field nr. ROG001, +15 October 2016 +; +RMNH +Por. 11656, +Mauritius +, +Rodrigues +, Mourouk Ebony, Castel Rock, +19.76203°S +63.46273°E +, depth +10 m +, scuba, coll. N.J. de Voogd, field nr. ROG060, +17 October 2016 +; +RMNH +Por. 11657, +Mauritius +, +Rodrigues +, Mourouk Ebony, Castel Rock, +19.76203°S +63.46273°E +, depth +10 m +, scuba, coll. N.J. de Voogd, field nr. ROG061, +17 October 2016 +; +RMNH +Por. 11658, +Mauritius +, +Rodrigues +, Mourouk Ebony, Castel Rock, +19.76203°S +63.46273°E +, depth +10 m +, scuba, coll. N.J. de Voogd, field nr. ROG062, +17 October 2016 +; +ZMA +Por. 13480, +Israel +, Gulf of Aqaba, Coral Garden, in cave at +1.5 m +depth, scuba, coll. M. Wunsch field nr. AQ139, +15 July 1998 +; +ZMA +Por. 13624, +Israel +, Gulf of Aqaba, Shark Observatory, depth +15 m +, scuba, coll. M. Wunsch field nr. RM201, +22 July 1998 +; +ZMA +Por. 21468, +Saudi Arabia +, Abu Madai Reef, +22.0609°N +38.7679°E +, depth +19 m +, scuba, coll. J. On On Lee, field nr. 4–8, +14 April 2009 +; +ZMA +Por. 12071, +Seychelles +, Amirantes, Alphonse Atoll, SE part of lagoon, +7.0333°S +52.7333°E +, depth +6–8 m +, scuba, coll. R.W.M. van Soest, field nr. +NIOP-E +stat. 788/08, +4 January 1993 +; +ZMA +Por. 12442, +Seychelles +, Amirantes, Platte Island Atoll, lagoon, +5.8333°S +55.35°E +, scuba, coll. R.W.M. van Soest, field nr. +NIOP-E +stat. 797, +7 January 1993 +; +ZMA +Por. 16369, +Madagascar +, Nosy Bé, Ambariobé, N of Nosy Komba, reef, depth +6–8 m +, scuba, coll. J.H. Stock, +28 December 1963 +; +ZMA +Por. 16372, +Madagascar +, Nosy Bé, S of Nosy Tanga, reef, depth +7–9 m +, scuba, coll. J.H. Stock, +1 January 1964 +; +ZMA +Por. 19251, +India +, + +Lakshadweep + +, Minicoy, depth +20 m +, scuba, coll. A. George +IERSE +, field nr. 91, +5 December 2004 +; +ZMA +Por. 19279, +India +, + +Lakshadweep + +, Kavaratti, depth +22 m +, scuba, coll. A. George +IERSE +, field nr. 20, +19 February 2005 +. + + + + +Description. +Because we recently provided an extensive description of Indonesian specimens of this species (cf. Van Soest & De Voogd 2015), we treat it here in summary format. Habitus in situ ( +Figs 43a–f +) is lobate, ovoid or irregularly massive, usually bright yellow in color (dull beige in preservation), with one or several prominent oscules with short rim. The oscule leads to a slit-like or more expanded atrial cavity. Surface optically smooth. Size of specimens up to 11 x 6 + +x +4 + +cm, often smaller. Consistency firm to hard. + + +Aquiferous system. +Leuconoid. + + +Skeleton. +( +Figs 44a–b +) The skeleton is formed by a dense mass of spicules surrounding the choanocyte chambers of the leuconoid aquiferous system. At the surface there are giant triactines in tangential position, numbers variable among individuals. The oscular rims are provided with smaller somewhat sagittal triactines, often with undulate paired actines. The atrial surface contains numerous tetractines, with their apical actines protruding into the atrial cavity. + + +Spicules. +( +Figs 44c–g +) Giant triactines, smaller triactines, tetractines. + + +Giant triactines ( +Fig. 44c +) with rather thin, sharply pointed actines, quite variable among the individuals, 480– +789 +–1380 +x 36 +– +61.8 +–114 µm. + + +Small triactines ( +Fig. 44d +), similarly sharply pointed, 78– +153 +–258 +x 6 +– +13.3 +–23 µm. Sagittal triactines ( +Fig. 44e +) of the oscular rim: 105– +123 +–144 µm +x 6 +– +11.1 +–17 µm. + + +Tetractines, with size and shape comparable to the small triactines, basal actines 121– +141 +–180 +x 8 +– +11.3 +–16 µm; apical actines, frequently with curved endings, 32– +87 +–170 +x 3 +– +7.4 +–12 µm. + + + + +Distribution and ecology. +Seychelles +, Red Sea, +India +, +Maldives +, +Madagascar +, +Rodrigues +; elsewhere throughout Indo-West Pacific tropical waters (see Wörheide +et al. +2008; Van Soest & De Voogd 2015); common on reefs down to + +25 m +. + + + + + +Remarks. +The actines of the giant triactines in the Western Indian Ocean on average are larger and thicker than those reported for Indonesian specimens (compare with Van Soest & De Voogd’s 2015 measurements). However, the smaller spicules are similar in size, so a conclusion that there is a distinct regional difference is not (yet) warranted. We obtained several partial 28S sequences, both from Indonesian and from +Rodrigues +specimens. + + +We also obtained a sequence of the Indonesian holotype of + +Ascoleucetta sagittata + +Cavalcanti +et al. +, 2013 + + +. In our phylogenetic tree of +Fig. 2C +the latter ended up in a larger clade of + +Leucetta chagosensis + +, closest to Indonesian specimens of that species. In a separate inspection of a trimmed alignment of 396 sites, the sequence of + +Ascoleucetta sagittata + +was found to be identical to three Indonesian specimens (one additional Indonesian specimen had one site different). The three Indonesian sequences and the + +Ascoleucetta sagittata + +sequence together differed in 2 sites from Western Indian Ocean specimens obtained from Rodrigues, and in 3 sites from the Maldives sequence of + +L. chagosensis + +. These results confirm the already suggested synonymy (cf. Van Soest & De Voogd 2015) of + +L. chagosensis + +and + +Ascoleucetta sagittata + +. + + +The differences between sequences from the Western Indian Ocean (excepting the +Maldives +) and Red Sea sequences obtained from Oliver Voigt showed a consistent single size difference, Indonesian and Red Sea differences amounted to 2 sites. + + +A sequence of the Australian + +Leucetta villosa +Wörheide & Hooper, 1999 + +downloaded from GenBank was also found to be included in the larger clade of + +L. chagosensis + +(cf. +Fig. 2C +). In the separate inspection mentioned above, the sequence of + +L. villosa + +differed in five/four sites from Indonesian and Western Indian Ocean + +L. chagosensis + +sequences. Because of the habitus differences (villous surface) this is interpreted as evidence of specific difference, indicating a possible species complex in + +L. chagosensis + +s.l. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC3AA57AFF678A63FAF6FCC5.xml b/data/38/6C/C6/386CC616DC3AA57AFF678A63FAF6FCC5.xml new file mode 100644 index 00000000000..6e30a38a602 --- /dev/null +++ b/data/38/6C/C6/386CC616DC3AA57AFF678A63FAF6FCC5.xml @@ -0,0 +1,443 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucascus schleyeri + +sp.nov. + + + + +Figures 41a–g +, +42a–h + + + + + +? + +Clathrina reticulum + +; + +Borojević 1967 +: 189 + +, fig. 2 (not: +Schmidt 1862 +). + + + + + +Clathrina +aff. +reticulum + +; + + +Rudi +et al. +2000 + +: 1434 + +. + + + + + + + +Material +examined. + +Holotype +, +ZMA +Por. 15734, +South Africa +, +Kwazulu Natal +, +Sodwana Bay +, +27.55°S +32.6833°E +, coral reef, depth + +22–27m + +, scuba, coll. +M. Schleyer +, field nr. +TASA53 +-S52, year 2000, undated. + + + + + +Description. +Massive lobate cormus ( +Fig. 41a +), consisting of densely and tightly anastomosed tubuli, with oscules on top of the lobes leading to atrial spaces. Color pink in situ. Preserved material consists of two fragments, each +2 x 2 x +1 cm +of the much larger specimen, estimated to be +6 x 4 x +2 cm +, most of which was used for natural products research. The preserved fragments are white or cream colored ( +Fig. 41b +) and comprise several contracted lobes. + + +Aquiferous system. +Asconoid, limited to the anastomosed tubuli. + + +Skeleton. +In cross section ( +Figs 41c–d +) the skeleton shows the dense arrangement of contracted tubuli of +0.1–0.2 mm +in diameter surrounding shallow atria ( +Fig. 41d +). The atrial walls are separated from the walls of the tubuli by their own layer of tri- and tetractines, as is visible in some parts of +Figs 41c–d +. There is a cortical surface layer ( +Figs 41e–f +) recognizable by the presence of erect banana-shaped diactines, detailed also in +Figs 15c–d +. The walls of the tubuli are built by several layers of triactines and tetractines. The latter protrude with their apical actines into the tubule lumen ( +Fig. 42a +). We noticed the presence of parasitic or commensal copepods in the cormus ( +Fig. 42b +). + + +Spicules. +( +Figs 42e–h +) Triactines and tetractines, the latter with spined apical actines. + + +Triactines ( +Fig. 42e +) equiradiate and equiangular, with cylindroconical actines measuring 54– +74.6 +– +90 x +4.5– +6.7 +–8.5 µm. + + +Tetractines ( +Figs 42f–g +) similar in shape and size to the triactines, occasionally somewhat sagittal, with thin straight apical actines provided with three rows of strong spines the position of which is matching the basal triradiate system ( + +Figs +42g + +), actines of the basal triradiate system 63– +78 +– +91 x 5 +– +6.5 +–8.5 µm, apical actines 31– +49 +– +76 x 2 +– +4.4 +–7 µm. + + +Diactines, asymmetrical, curved, ‘banana’-shaped, often eroded (probably artefactual) and grooved, 48– +76 +– +98 x 8 +– +9.6 +–12 µm. + + + + +Distribution and ecology +. Natal coast of + +South +Africa + +, deep reef. + + + + +Etymology. +Named after Dr Michael Schleyer, Oceanographic Research Institute, Durban, + +South +Africa + +, who collected the material, and in recognition of his important work on the marine ecology of + +South +Africa + +. + + + + +Remarks. +Although we do not have molecular sequence data for this specimen, the overall similarity of the present material with + +Leucascus +, + +reviewed by Cavalcanti +et al. +(2003), makes it likely that the present new species is also a member of that genus. Our SEM cross sections ( +Figs 41c–d +) show the characteristic structure of short atrial cavities surrounded by tightly anastomosed tubuli, with the whole cormus covered with a cortex of erect short diactines. Of the described species of + +Leucascus + +, only +South +Australian + +L. clavatus +Dendy, 1892 + +possesses diactines, but these are much larger and thicker (350–850 +x 99 +–140 µm) than those of the new species, while also the tri- and tetractines are significantly larger (actines 70–160 +x 9–19 +µm). + + + +FIGURE 41. + +Leucascus schleyeri + + +sp.nov +. + +, holotype ZMA Por. 15734, a, habitus in situ on the deep reef of Sodwana Bay, Kwazulu Natal, South Africa (photo M. Schleyer), b, preserved fragments of holotype (scale bar = 1 cm), c, SEM image of cross section of cormus showing dense mass of tubuli, d, detail of c showing shallow pseudoatrium, e, SEM image of overview of surface, f, detail of e showing erect diactines. + + + + +FIGURE 42. + +Leucascus schleyeri + + +sp.nov +. + +, holotype ZMA Por. 15734, a, SEM image of wall of tubulus with protruding apical actines of tetractines, b, SEM image of parasitic or commensal copepods lodged in the cormus, c, SEM image of perpendicular section of the upper surface showing crowded ‘banana’-shaped erect diactines, d, light microscopic image of the same, e–h, SEM images of spicules, e, triactine, f, tetractines, g, details of apical actines of tetractines, h, ‘banana’-shaped diactines from the upper surface. + + + +Borojević (1967) +reported + +Ascaltis reticulum +( +Schmidt, 1862 +) + +(as + +Clathrina + +) from + +South +Africa + +, from both the Indian Ocean coast (‘Natal shore’) and from the Atlantic coast (False Bay). He gave a general description for these specimens, which fits our material except for the diactines, which measured 100–200 +x 15–20 +µm, well in excess of our diactines. +No +mention was made of spines on the apical actines of the tetractines. + +A. reticulum + +is originally described from the Mediterranean ( +Schmidt, 1862 +). It is possible that at least the Natal specimens could be conspecific with our specimen rather than with + +A. reticulum + +. Klautau +et al. +(2016) redescribed Adriatic + +Ascaltis reticulum +( +Schmidt, 1862 +) + +and provided molecular sequence data. The spicule +types +and sizes described by Klautau +et al. +conform rather closely to those cited above for our specimen, except for the diactines which were longer and thinner (60–142 +x 4–6 +µm) and not eroded. Of course, + +Ascaltis + +differs from + +Leucascus + +in lacking a lined atrial cavity ( + +Borojević +et al. +2002a + +), and generally is less elaborate in shape and structure. Molecular sequence data of + +Ascaltis reticulum + +provided by Klautau +et al. +(2016), and downloaded from GenBank were found to group at a rather low bootstrap value with sequences of the Indonesian + +Leucascus flavus + +described by us previously (Van Soest & De Voogd, 2015) in our Calcinea phylogeny ( +Fig. 2C +). This would confirm a close relationship of + +Ascaltis + +and + +Leucascus + +as postulated by + +Borojević +et al. +(2002a) + +. Nevertheless, there are no molecular sequence data available for the +type +species of + +Ascaltis + +, + +A. lamarcki +( +Haeckel, 1872 +) + +, so the true affiliation of + +Leucascus + +and + +Ascaltis + +remains uncertain. + + +Dendy’s (1913) + +Leucosolenia gardineri + +from the +Western +Indian Ocean on paper looks close to the present new species, the major obvious difference appearing to be the lack of banana-shaped diactines in + +L. gardineri +. + +The species is currently assigned to + +Ascaltis + +. + + +Novel natural products, clathculins A and B, have been described from this specimen by + +Rudi +et al. +2000 + +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC3DA560FF678892FDF0FC75.xml b/data/38/6C/C6/386CC616DC3DA560FF678892FDF0FC75.xml new file mode 100644 index 00000000000..798119186a0 --- /dev/null +++ b/data/38/6C/C6/386CC616DC3DA560FF678892FDF0FC75.xml @@ -0,0 +1,300 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucetta microraphis +Haeckel, 1872 + + + + + +Figs 45a–f +, +46a–e + + + + + + +Leucetta primigenia +var. +microraphis + +Haeckel, 1872 +: 119 + + +, pl. 21 figs 10–17. +? + +Leucandra primigenia +var. +microraphis + +; + +Row 1909 +: 186 + +. + +Leucetta microraphis + +; Van Soest & De Voogd 2015: 54, figs 39a–d, 40a–d, with further synonyms. +Material examined. +RMNH Por. 8318, Mayotte, Ankazoberavina, Roland Point, 12.9731°S 44.9793°E, coll. A. Bialecki, field nr. +MAY01 +-018, +4 May 2013 +; RMNH Por. 8341, Mayotte, Passe Boueni Sud, 12.9265°S 44.9668°E, coll. A. Bialecki field nr. +MAY03-41 +, +5 May 2013 +; RMNH Por 8717, Madagascar, Riva Be, 12.9849°S 48.3910°E, depth +2–3 m +, coll. A. Bialecki, field nr. MAD12-IM047, +27 December 2012 +. + + + + + +FIGURE 45. + +Leucetta +microraphis +Haeckel, 1872 + +, from Mayotte and Madagascar, a–d, habitus in situ (photos N.J. de Voogd and A. Bialecki), a, Mayotte RMNH Por. 8341, b, ditto, c, Mayotte RMNH Por. 8318, d, Madagascar RMNH Por. 8717, e, Mayotte RMNH Por. 8341, on deck, f, Mayotte RMNH Por. 8341, SEM image of overview of the spicules showing giant and small triactines from the main skeleton, and tetractines (arrows) from the atrial wall. + + + + +FIGURE 46. + +Leucetta +microraphis +Haeckel, 1872 + +, RMNH Por. 8318 from Mayotte, a, light microscopic overview of surface skeleton, b–e, SEM images of the spicules, b, giant triactine, c, small triactines, largest sizes, c1, small triactines, smallest sizes, d, tetractines, e, detail of apical actine of tetractine. + + + + +Description. +Because this species was extensively treated recently by Van Soest & De Voogd (2015), we provide here only a summary treatment. The in situ habitus ( +Figs 45a–d +) with its pinkish red-green-brown masses of tubular outgrowths with lighter colored undersides and tube rims, is quite characteristic, leaving no doubt that it is conspecific with Indonesian specimens previously described by us. Tubular outgrowths are +3–6 cm +high and +1–2 cm +in diameter. Surface optically smooth, but rough. Consistency is firm. On deck habitus ( +Fig. 45e +) similar in color to in situ habitus. + + +Aquiferous system +. Leuconoid + + +Skeleton. +( +Figs 45f +, +46a +) A dense mass of triactines of various sizes, with tetractines lining the atrial cavities. Giant triactines concentrated at the surface. + + +Spicules. +( +Figs 46b–d +) These include a large size range of giant triactines, small triactines, and tetractines. + + +Giant triactines ( +Fig. 46b +), equiradiate, equiangular, actines measuring 480– +846 +–1260 +x 65 +– +107 +–155 µm + + +Small triactines ( +Figs 46c,c +1 +), equiradiate, equiangular, possibly in two overlapping sizes, actines measuring overall 124– +171 +–216 +x 10 +– +15.1 +–22 µm. + + +Tetractines ( +Figs 46d +), basal triadiate system with actines 78– +119 +–148 +x 8 +– +10.3 +–12 µm, apical actines wobbly ( +Fig. 46e +) or curved, relatively small and thin 14– +36 +– +48 x 4 +– +5.7 +–7 µm. + + + + +Distribution and ecology. + +Mayotte + +, +Madagascar +, +Red Sea +, +Indonesia +, +Australia +, + +Papua +New Guinea + +, +New Caledonia +, on reefs in shallow depths. + + + + +Remarks. +This species is reported throughout the Indo-West Pacific tropical region, but the identities of all these records need critical re-examination. The present specimens conform closely in habitus and color to the Indonesian specimens described by us previously (Van Soest & De Voogd 2015), but the giant triactines are smaller and thinner in the present specimens. The habitus does not seem to match in some aspects with e.g. Wörheide & Hooper’s (1999) Australian record and with + +Voigt +et al. +’s (2017) + +Red Sea +records, as these specimens lack the redbrown-greenish pink-with-white coloration characteristic of our concept of this species. Spicule sizes of the triactines of these latter records do match better with those of the present specimens. Critical comparison with uniformly pinkish white specimens is made below. + + +We obtained partial 28S rRNA sequences from several +Western +Indian Ocean specimens ( + +Mayotte + +and +Madagascar +), downloaded several more from +Indonesia +and + +Australia +. Oliver Voigt’s +Red Sea + +sequences were made available to us. All are presented in +Fig. 2C +. They are discussed below in the Remarks of a new species, + +L. sulcata + + +sp.nov. + +from +Rodrigues +. + + +Row’s (1909) records of two specimens from the northern and southern parts of the +Red Sea +were not described, so these remain +incertae sedis +. + + + +Thacker +et al. +(2013) + +reported the West Indian species + +Leucetta primigenia +Haeckel, 1872 + +from Malaysia. This likely concerns + +Leucetta microraphis + +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC41A502FF678B4EFCCBFA7F.xml b/data/38/6C/C6/386CC616DC41A502FF678B4EFCCBFA7F.xml new file mode 100644 index 00000000000..f7de13f99fe --- /dev/null +++ b/data/38/6C/C6/386CC616DC41A502FF678B4EFCCBFA7F.xml @@ -0,0 +1,173 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Clathrina repens + +sp.nov. + + + + +Figures 26a–d + + + + + + +Material +examined. + +Holotype +, +RMNH +Por. 10161a, +Maldives +, +Faafu Atoll +, +Wallstreet +, +3.119°N +72.979556°E +, depth + +10 m + +, scuba, coll. +N.J. de Voogd +, field nr. +MAD10 +/MAS122, + +20 February 2015 + +. + + + + + +Description. +Open network of creeping and upright tubuli, covering the surface of a keratose sponge ( + +Hyrtios + +sp.) ( +Fig. 26a +), size several cm2. A second specimen ( +Fig. 26a +1 +, not collected) encrusted an ascidian. Individual tubuli approximately +2 mm +high and +1 mm +diameter. Upright tubuli often open-ended, presumed to be oscules. Color shades of dull orange, pink-orange and beige; pale beige in preservation ( +Fig. 26b +). + + +Aquiferous system. +Asconoid. + + +Skeleton. +( +Fig. 26c +) Walls of tubuli with a single layer of spicules. + + +Spicules. +( +Fig. 26d +) Triactines with conical actines, variable in length, 66– +97 +–129 +x 6 +– +7.4 +–9 µm. + + + + +Distribution and ecology +. +Maldives +, coral reef, + +10 m +. + + + + + +Etymology. +Repens (L.) means creeping, referring to the reticulation of small tubuli closely adhering to the substratum. + + + + +Remarks. +Morphologically, this appears a unique species. Its habitus and spicule sizes show similarity to Indonesian + +Arturia tubuloreticulata +Van Soest & De Voogd, 2015 + +, but this has a minority of tetractines. We examined the present specimen exhaustively, but could find no tetractines. + +Unfortunately, no sequences were obtained from it. + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC41A507FF678E33FE2CF991.xml b/data/38/6C/C6/386CC616DC41A507FF678E33FE2CF991.xml new file mode 100644 index 00000000000..6b0fb882d07 --- /dev/null +++ b/data/38/6C/C6/386CC616DC41A507FF678E33FE2CF991.xml @@ -0,0 +1,398 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Clathrina +aff. +pulcherrima +( +Dendy, 1891 +) + + + + + +Figures 27a–e + + + + + +? + +Leucosolenia pulcherrima + +Dendy, 1891 +: 52 + + +, pl. I fig. 7, pl. IV fig. 3, pl. X fig.3. + + + + +? + +Clathrina blanca + +; + +Jenkin 1908 +: 438 + +, figs 85–87 (not: +Miklucho-Maclay 1868 +) + + + + + +? +Clathrina blanca + +f. + +pulcherrima + +; + +Borojević 1967 +: 191 + +(? not: +Dendy 1891 +) + + + + + +Material examined. +ZMA +Por. 22408c, +Mozambique +Channel, between +Mozambique +and +Madagascar +, E of Juan de Nova +Island +, +17.2817°S +43.1567°E +, depth +60 m +, trawl, coll. RV‘Pelagia’ Around Africa II expedition, field nr. 20- +ASC +10, 1 April +2001. + + + + +Description. +Stalked + +Guancha + +-like sponge with flattened cormus ( +Fig. 27a +) consisting of a tightly anastomosed mass of thin tubuli. The upper rim of the cormus has a row of tiny oscules ( +Fig. 27a +1 +). Size entire specimen +3.3 cm +high, stalk +1.8 cm +long and +0.17 cm +thick, cormus +1.3 cm +wide, +0.4 cm +thick. Tubuli about +0.05–0.1 mm +in thickness, with thicker tubuli running the entire length of the cormus. Color in alcohol dirty white to light beige. + + + +FIGURE 26. + +Clathrina repens + + +sp.nov. + +, a, in situ habitus of holotype RMNH Por. 10161 from the Maldives, a1, in situ habitus of a second specimen (not collected) (photos N.J. de Voogd), b, preserved holotype (scale bar = 1 cm), c, light microscopic image of one of the tubuli, d, SEM images of the spicules. + + + + +FIGURE 27. + +Clathrina +aff. +pulcherrima +(Dendy, 1891) + +, a, habitus of preserved specimen from Mozambique Channel W of Madagascar (scale bar = 1 cm), a1, detail of head with row of oscules on the rim, b, light microscopic image of skeleton of the basal part of the head, showing aligned parasagittal spicules, c–e, SEM images of the spicules, c, equiradiate triactine with thin actine, d, ditto with thick conical actines, e, various shaped parasagittal triactines. + + + +Aquiferous system. +Asconoid. + + +Skeleton. +( +Fig. 27b +) Stalk and outer tubule walls consist of strongly sagittal triactines and to a lesser extent regular triactines; inner tubuli predominantly have regular triactines in their walls. + + +Spicules. +( +Figs 27c–e +) Triactines only. + + +Triactines, in two distinct +types +, (1) equiradiate equiactinal triactines ( +Fig. 27c +) with thin cylindrical actines 59– +101 +–126 +x 5 +– +6.3 +–8 µm, occasionally slightly sagittal with thicker conical actines ( +Fig. 27d +), and (2) strongly sagittal (parasagittal) triactines ( +Figs 27e +), with conical actines, with unpaired actines usually thicker halfway, paired actines usually tapering gradually, but occasionally also thicker halfway, unpaired actines strongly variable in length, 151– +226 +–267 x 7.5– +11.5 +–13 µm, paired actines 61– +114 +–140 +x 7 +– +10.1 +–12 µm. + + + + +Distribution and ecology. +Mozambique +Channel, possibly SE coast of + +South +Africa + +, possibly Southeast +Australia +, shallow water to +60 m +depth. + + + + +Remarks. +The shape of this specimen closely resembles the description and drawing of the Southeast Australian species + +Clathrina pulcherrima +Dendy, 1891 + +(see +Dendy, 1891 +, p. 52, pl. I fig. 7, as + +Leucosolenia + +). This is likewise a stalked sponge with upper body of laterally compressed oval shape, with the upper rim provided with a row of oscules. The spicules are also divisible in regular equiradiate and equiangular triactines and parasagittal triactines. However, there is a significant difference in the lengths of the actines: the equiradiate actines measure +84 x +4.2 µm, the parasagittal unpaired actines are 100 +x 8 +µm long and the paired actines are +56 x 8 +µm. Although Dendy did not give ranges of the actines, it is clear from these data that the spicules are distinctly shorter and thinner than the present ones. It is currently judged to be uncertain whether this difference merits specific distinction. + + +Jenkin (1908) +reported a flattened specimen of + +Clathrina blanca +( +Miklucho-Maclay, 1868 +) + +from + +Zanzibar + +, which reminds of our specimen, but is more irregular and the stalk is not a separately developed structure. It likewise has two +types +of triactines, regular triactines with actines of 60–100 +x 4–9 +µm and sagittal triactines with long unpaired actines of 100–160 +x 7–11 +µm. These measurements are somewhat inbetween those of Dendy and ours. + +Clathrina blanca + +is not flattened and is confined to the North Atlantic. + + +Borojević (1967) +described specimens from + +South +Africa + +(East London and Durban) as + +Clathrina blanca + +forma + +pulcherrima + +, but since he did not give spicule measurements, nor illustrations, it is not certain his specimens belonged to the same species as the present. He also signaled the presence of tripods, shaped similar to the regular triactines but with raised centre, which were not clearly present in the above-described specimen. + + +Haeckel (1872) +reported (p. 16) and illustrated (his pl. 2 figs 5 and 6) stalked + +Clathrina primordialis + +specimens from the Red Sea, which he obtained from Miklucho-Maclay with the manuscript name ‘ + +Nardoa arabica + +’. The specimens had only a single oscule and the spicules were all regular triactines. +Row (1909) +also reported + +C. primordialis + +but gave no description or illustration. Recently, Klautau +et al. +2016 redescribed + +C. primordialis + +from the Adriatic and restricted that species to the Mediterranean. The identity of the Red Sea population referred to by Haeckel and Row remains uncertain. + +Voigt +et al. +2017 + +stated that it possibly was conspecific with their + +Clathrina rowi + +. + + +Although there is no morphological similarity, molecular sequence analysis of partial 28SrRNA put this species closest to + +Clathrina rotundata + +Voigt +et al +., 2017 + + +. Still, a trimmed alignment with length of 395 sites showed 45 site differences between the present species and + +C. rotundata + +. This result merely expresses the isolated positions of these two species. + + + + + +Guancha +Miklucho-Maclay, 1868 + +, for a long time used for stalked + +Clathrina + +- +type +sponges, has been synonymized with + +Clathrina + +s.s. +because its +type +species + +C. blanca + +conforms to the new definition of + +Clathrina + +. However, it is quite possible that a species group of that genus with the combination of stalked habitus and differentiated regular and long-unpaired actine sagittal triactines deserves to be recognized at the genus level. This is not further elaborated here. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC43A502FF678F3EFC61FD69.xml b/data/38/6C/C6/386CC616DC43A502FF678F3EFC61FD69.xml new file mode 100644 index 00000000000..5a43506ec9a --- /dev/null +++ b/data/38/6C/C6/386CC616DC43A502FF678F3EFC61FD69.xml @@ -0,0 +1,266 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Clathrina maremeccae + +sp.nov. + + + + +Figures 25a–c + + + + + +Material examined. +Holotype +, +RMNH +Por. 9662, +Saudi Arabia +, +Jeddah +, near +Thuwal +, +Um Albalam +, +22.193556°N +38.9475°E +, scuba, coll. +N.J. de Voogd +, field nr. THU10/JED166, + +12 November 2014 + +. + + + + + +FIGURE 25 +. + +Clathrina maremeccae + + +sp.nov. + +, holotype RMNH 9662 from Saudi Arabia, Jeddah, a, habitus on deck (photo N.J. de Voogd), b, light microscopic image of the cormus, c, SEM images of triactines. + + + + +Description. +Cormus clathroid ( +Fig. 25a +), forming a loosely anastomosed small mass of tubuli +0.2–1 mm +in diameter leading to a few wider oscules. The single specimen is 15 x 8 + +x +4 + +mm in size. +No +evident water-collecting tubes. Color pale yellow, based on an on deck photo as there is no in situ photo. + + +Skeleton. +( +Fig. 25b +) The tubule walls have a single layer of overlapping triactines. + + +Spicules. +( +Figs 25c +) Equiradiate and sagittal triactines, with cylindrical actines, ending in often slightly swollen, blunt endings. Actines 67– +127.8 +–165 +x 5 +– +6.4 +–7.5 µm. A few broken trichoxeas are considered foreign. + + + + +Distribution and ecology. +Saudian part of the +Red Sea +, on reefs. + + + + +Etymology. +The name refers to the +type +locality, the +Red Sea +, which was named Mare +Mecca +by historical geographers (Wikipedia.org). + + + + +Remarks. +The new species resembles +Red Sea + +Clathrina rotundata + +Voigt +et al. +, 2017 + + +both in morphological aspects (loosely clathroid and with cylindrical actines of the triactines), and in a molecular sense as this species, based on partial 28SrRNA, also falls outside the larger clades of + +Clathrina + +species in our phylogenetic tree of +Western +Indian Ocean + +Clathrina + +species ( +Fig. 2A +). However, there are also compelling reasons not to assign the present specimen to + +C. rotundata + +. Morphologically, the on deck photo shows a pale yellow color, whereas + +C. rotundata + +is white, and the upper actine length of the triactines is considerably higher than that of + +C. rotundata + +(165 vs. 123 µm). Molecularly, according to our phylogenetic analysis, the two species are not closely related. In a separate trimmed alignment of the two species of 382 sites length, + +C. maremeccae + + +sp.nov. + +and + +C. rotundata + +differed in 49 sites. + + +There is considerable morphological similarity with Indonesian + +Clathrina beckingae +Van Soest & De Voogd, 2015 + +, which has the same shape and tube diameter, colors also white and cream in various specimens, and equiradiate triactines with cylindrical actines. Differences are the presence of distinct water-collecting tubes and the absence of sagittal spicules in + +C. beckingae + +. Actine sizes of the triactines are also considerably smaller than those in + +C. maremeccae + + +sp.nov +. + +(up to 103 µm in + +C. beckingae + +). We obtained partial 28srRNA sequences for this Indonesian material, and found that it differed in a separate trimmed 28S rRNA alignment of 382 sites length in 26 different sites. + + +No +closely related species were identified in our partial 28SrRNA tree ( +Fig. 2A +). + + +At the suggestion of one of the reviewers, we obtained an ITS sequence (not submitted to GenBank) for this species and in an analysis (not shown here) of ITS sequences of + +Clathrina + +species that appeared highly similar in a BLAST attempt, downloaded from GenBank, we noted that the new species ended up in a highly supported clade with +Clathrin +a sp. 4 and sp. 5 sensu Klautau +et al. +2013, respectively a species from the Caribbean and from +French Polynesia +. A trimmed alignment of 556 sites of the three species showed 35 site differences between + +C. maremeccae + + +sp.nov. + +and +C. +sp. 4, and 21 site differences with +C. +sp. 5. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC44A50BFF678EA9FEE3FF61.xml b/data/38/6C/C6/386CC616DC44A50BFF678EA9FEE3FF61.xml new file mode 100644 index 00000000000..d344d60fd1e --- /dev/null +++ b/data/38/6C/C6/386CC616DC44A50BFF678EA9FEE3FF61.xml @@ -0,0 +1,363 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + +Ernstia + +arabica + +Voigt +et al. +, 2017 + + + + + + +Figures 28a–c +, +29a–c +, +30a–e + + + + + +Ernstia + +arabica + + +Voigt +et al. +, 2017 + +: 9 + + +, figs 5a–e. + + + + + + + +Material +examined. + +ZMA +Por. 13640, +Israel +, +Coral Garden +, +Gulf +of Aqaba, depth + +1.5 m + +, scuba, coll. +M. Wunsch +, field nr. AQ140, + +15 July 1998 + + +; + +ZMA +Por. 13642, +Egypt +, +Ras Mohammed +, +Shark Observatory +, depth + +15 m + +, scuba, coll. +M. Wunsch +, field nr. +RM +222, + +23 July 1998 + + +. + + + + +Description. +There are two, rather different specimens from the +Gulf +of Aqaba, which are assumed to be members of this species. Because of the differences we describe them separately. Cormus of ZMA Por. 13640 ( +Fig. 28a +) small yellow cushions connected by thinner stolon-like parts, structure compact made up of tightly anastomosed thin tubuli ( +Fig. 28b +). Oscules centrally located on the cushions and slightly elevated. Lateral size of cormus up to 2.5 + +x +1 + +cm, thickness about +5–8 mm +. ZMA Por. 13642 is a flatly encrusting cormus ( +Fig. 30a +) consisting of tightly anastomosed thin tubuli. Pale yellow in life, dirty white in alcohol. Several broader tubuli lead to a few wide oscules slightly raised above the cormus. Lateral size 5 + +x +4 + +cm. Constency soft. + + +Aquiferous system. +Asconoid. + + +Skeleton. +( +Figs 28b–e +) Walls of tubuli in both specimens are thin ( +Fig. 28c +), consisting of one–two spicule layers ( +Figs 28d +, +30b +) with a mixture of tri- and tetractines; the apical actines of the latter are protruding into the tubule lumina ( +Fig. 28c +) forming a dense palisade ( +Fig. 28e +). Consistency firm. + + + +FIGURE 28. +Ernstia + +arabica +Voigt +et al. +2017 + +, ZMA Por. 13640, from the Gulf of Aqaba, a, habitus in situ (photo M. Wunsch), b–e, SEM images of sections of the cormus, b, overall section showing tightly anastomosed tubuli, c, cross section of tubuli showing apical actines of tetractines protruding in the tubar lumen, d, cross section of the surface region, e, detail of tubar lumen and protruding apical actines. + + + + +FIGURE 29. +Ernstia + +arabica +Voigt +et al. +2017 + +, ZMA Por. 13640, from the Gulf of Aqaba, SEM images of the spicules, a, triactine, b, tetractines, c, detail of apical actine of tetractine. + + + +Spicules. +( +Figs 29a–c +, +30c–e +) Triactines and tetractines, the latter present in clearly larger numbers. +No +distinct trichoxeas were found. + +Triactines equiradiate and equiangular, with conical actines, some verging toward tripod-shape. + +Actine sizes of ZMA Por. 13640 ( +Fig. 29a +) measure 89– +98 +–105 +x 9 +– +11.2 +–13 µm. + + +Actine sizes of ZMA Por. 13642 ( +Figs 30c +) measure 102– +125 +–165 +x 11 +– +16.4 +–26 µm. + +Tetractines of similar shape and size to the triactines, equiangular, with conical actines. + +Actines of the basal triradiate system in ZMA Por. 13640 ( +Figs 29b +) measure 87– +94 +– +99 x 9 +– +10.3 +–12 µm, apical actines ( +Fig. 30c +) smooth, straight, 66– +76 +– +91 x 5 +– +6.6 +–8 µm. + + +Actines of the basal triadiate system in ZMA Por. 13642 measure ( +Figs 30d +) 67– +127 +–182 +x 9 +– +15.2 +–27 µm; apical actines ( +Fig. 30e +) shorter, thinner and sharper, 23– +38 +– +59 x 3 +– +5.7 +–11 µm. + + + + +Distribution and ecology. +Israelian +Red Sea +, Saudi Arabian and Egyptian +Red Sea +( + +Voigt +et al. +2017 + +), down to + +15 m +. + + + + + +Remarks. +The present specimens closely resemble the +type +in most aspects, except for the absence of trichoxeas. These were also not consistently present in the +type +material ( + +Voigt +et al. +2017 + +). A small further difference is the length of the apical actine of the tetractines, which has a greater range in the +type +material (up to 156 µm). The two present specimens differ subtly in the habitus and the smaller-thinner vs. the larger and more robust spicules. + +Voigt +et al. +(2017) + +described and measured the spicules of specimens from the +Northern +and + +Southern +Red Sea + +and found triactines and tetractines having actine lengths between 38 and 116 µm, and apical actines between 56 and 156 µm, while our own specimens have these data respectively 67–182 µm and 23–91 µm. + + + +FIGURE 30. +Ernstia + +arabica +Voigt +et al. +2017 + +, ZMA Por. 13642, from Northern Red Sea, Egypt, Ras Mohammed, a, habitus in situ on the reef (photo M. Wunsch), b, light microscopic image of a detail of the cormus, c–e, SEM images of the spicules, c, triactines, d, tetractines, e, detail of apical actine of tetractine. + + + +Unfortunately, we were unable to obtain partial 28S rRNA sequences for these specimens. Below we compare + +E. +arabica + +with +Western +Indian Ocean specimens identified as the closely related +Ernstia naturalis +Van Soest & De Voogd, 2015. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC53A512FF678A2EFDA0F86A.xml b/data/38/6C/C6/386CC616DC53A512FF678A2EFDA0F86A.xml new file mode 100644 index 00000000000..1a780cecaaf --- /dev/null +++ b/data/38/6C/C6/386CC616DC53A512FF678A2EFDA0F86A.xml @@ -0,0 +1,454 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Borojevia pirella + +sp.nov. + + + + +Figures 12a–b +, +13a–e + + + + + + +Material +examined. + +Holotype +, +RMNH +Por. 11622a, +Mauritius +, +Rodrigues +, +Passe Baladirou +, +19.6683°S +63.46307°E +, depth + +12 m + +, scuba, coll. +N.J. de Voogd +, field nr. ROG023, + +16 October 2016 + +. + + + + +Paratype +, +RMNH +Por. 11622b, +Mauritius +, +Rodrigues +, +Passe Baladirou +, +19.6683°S +63.46307°E +, depth + +12 m + +, scuba, coll. +N.J. de Voogd +, field nr. ROG023, + +16 October 2016 + +. + + + + + +Description. +Small pear-shaped cormus ( +Figs 12a–b +) consisting of a mass of moderately tightly anastomosed tubuli separated by rounded or polyangular spaces. Color white, semitransparent. Size approximately +1.5 cm +high, +1 cm +in diameter. Tubuli approximately +0.2 mm +in diameter. The narrow end is provided with an oscule of about +2 mm +diameter, leading into a short water-collecting tube and a pseudoatrium. Preserved material consists of two specimens ( +Figs 12a +1 +, +holotype +, and 12b1, +paratype +), which collapsed to form flattened objects with soft consistency. + + +Aquiferous system. +Asconoid. + + +Skeleton. +The pseudoatrium has no special skeleton, it is merely a space between the anastomosed tubuli ( +Fig. 13a +). The wall of these is thin, having one or two spicules comprising a mixture of triactines and tetractines, the latter with the apical actines protruding into the lumen of the tubuli. + + +Spicules. +( +Figs 13b–e +) Triactines and tetractines of approximately the same size, no differentiated larger and smaller triactines are present. + + +Triactines ( +Fig. 13b–c +) equiangular and equiradiate ( +Fig. 13b +), with a tendency to become slightly sagittal, with a longer unpaired actine; occasionally triactines are irregular with one of the actines wavy and distinctly sagittal ( +Fig. 13c +). Actine dimensions 51– +81.3 +– +93 x 5 +– +6.7 +–8 µm. + + +Tetractines ( +Fig. 13d–e +), similar in size and shape to the triactines ( +Figs 13d +), with apical actines provided with three prominent conical spines in one verticil the position of which is matching the basal triradiate system ( +Figs 13e +). Actines of the basal triadiate system 72– +85.7 +– +96 x +5.5– +7.1 +–8 µm, apical actines 31– +58.4 +– +76 x 5 +– +5.9 +–7 µm. + + + + +Distribution and ecology. +Rodrigues +, Mascarene Islands, on coral reefs at +12 m +depth. + + + + +Etymology. +Pirella (L.), a feminine noun, meaning a small pear, referring to the habitus of the sponge. + + + + +Remarks. +Despite the presence of a pseudoatrium and spined apical actines of the tetractines, molecular sequence data indicate clearly ( +Fig. 2B +) that this species is closely related to + +Borojevia +aff. +cerebrum + +and ‘ + +Ascaltis + +OV-2012’, both reassigned to + +Borojevia + +(cf. Klautau +et al. +2016), and not to + +Ascaltis reticulum + +. + +Voigt +et al. +’s (2012) + +Australian species ‘ + +Ascaltis + +OV 2012’ has a clear pseudoatrium illustrated in their Supporting +Fig. S1 +inset J, but its sequence is grouped unequivocally among the + +Borojevia + +’s in our +Fig. 2B +phylogeny. This justifies assignment of the present species to the genus + +Borojevia + +. The triactine complement of + +B. pirella + + +sp.nov. + +does not contain any clear tripods, as is one of the additional features described for the genus + +Borojevia + +. The presence of the pseudoatrium is shared with the above described + +B. tubulata + + +sp.nov +. + +, but apparently is absent in + +B. voigti + + +sp.nov. + +and other + +Borojevia + +spp. The relationship with + +Ascaltis + +remains unresolved. The three prominent spines on the apical actines of the tetractines are a special feature of the new species. It is shared with the recently described Brazilian + +Borojevia trispinata + +Azevedo +et al. +, 2017 + + +. This is generally similar in spicule sizes, but on average has slightly smaller actines. The habitus differs in lacking a central pseudoatrium and being more irregular in shape, not pear-shaped. + + +We obtained sequences for + +Borojevia tubulata + + +sp.nov. + +(both +holotype +and non-type +Seychelles +specimen, cf. above) and + +Borojevia pirella + + +sp.nov. + +(both +holotype +and +paratype +). We compared these with two sequences of +Red Sea +specimens of + +Borojevia +aff. +aspina + +provided by Oliver Voigt in a separate restricted phylogenetic analysis. The aligned and trimmed sequences (length 426 sites) revealed that both identical sequences of + +B. pirella + + +sp.nov. + +showed 4–5 sites difference with + +B. +aff. +aspina +sensu + +Voigt +et al. +2017 + + +, 12–22 sites difference with + +B. tubulata + + +sp.nov. + +(the higher difference being with the +Seychelles +specimen, as the +holotype +and Voigt’s + +Borojevia + +sp. have identical sequences). It may be concluded that the new species and + +Borojevia +aff. +aspina + +are more closely related than each of them with + +B. tubulata + + +sp.nov. + + + + +FIGURE 12. + +Borojevia pirella + + +sp.nov. +, + +a, habitus in situ of holotype RMNH Por. 11622, from Rodrigues, the easternmost of the Mascarene Islands (photo N.J. de Voogd), a1, preserved holotype (scale bar = 1 cm), b, habitus in situ of paratype RMNH Por. 11622b (photo N.J. de Voogd), b1, preserved paratype. + + + + +FIGURE 13. + +Borojevia pirella + + +sp.nov. +, + +holotype RMNH Por. 11622, from Rodrigues, a, light microscopic cross section of oscular region showing pseudoatrium and surrounding tubuli, b–e, SEM images of the spicules, b, regular triactine, c, rare sagittal irregular triactine, d, tetractines, e, details of apical actines of the tetractines showing characteristic verticil of three conical spines. + + + +Molecular comparison of + +B. pirella + + +sp.nov. + +with the similar Brazilian species + +B. trispinata + +is complicated by differences in the target genes (our 28S vs + +Azevedo +et al. +2017 + +’s ITS). In a special effort, we obtained additional ITS data for + +B. pirella + + +sp.nov. + +and aligned two ITS sequences ( +holotype +and +paratype +, which appeared to be identical, not submitted to GenBank) with two sequences of + +B. trispinata + +downloaded from GenBank (UFRJPOR6419 and 6487, showing several site differences). A trimmed 792 sites alignment of the four sequences shows considerable differences (25 non–conserved sites differed between the two species, not counting a gap of 27 sites). Nevertheless, the morphological resemblance of the two species from the +Western +Indian Ocean and the +Western +Atlantic Ocean region is striking. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC54A518FF678D6AFE91FED9.xml b/data/38/6C/C6/386CC616DC54A518FF678D6AFE91FED9.xml new file mode 100644 index 00000000000..430f3ac0225 --- /dev/null +++ b/data/38/6C/C6/386CC616DC54A518FF678D6AFE91FED9.xml @@ -0,0 +1,313 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Clathrina rowi + +Voigt +et al., +2017 + + + + + + +Figures 16a–c +, +17a–c + + + + + + +Clathrina rowi + + +Voigt +et al. +, 2017 + +: 14 + + +, fig. 8. + + + + + + + +Material +examined. + +RMNH +Por. 10002, +Saudi Arabia +, +Jeddah +, near +Thuwal +, +Tahlah +, +22.25725°N +38.880917°E +, scuba, coll. +N.J. de Voogd +, field nr. THU14/JED209, + +13 November 2014 + + +; + +ZMA +Por. 13446, +Israel +, +Gulf of Aqaba +, +North Pinnacle +, in cave, depth + +9 m + +, scuba, coll. +M. Wunsch +, field nr. AQ52, + +4 July 1998 + + +. + + + + +Description. +The RMNH Por. 10002 specimen in situ ( +Fig. 16a +) is an overall loose mass of intermediate-sized tubuli, provided with several water-collecting tubes ending in oscules. Cormus anastomosed in places to densely connected smaller tubes. Individual tubes +0.4–2 mm +in diameter. Color pale beige to dirty white, semi-transparent. Preserved specimen massive due to compression of tubules during preservation and manipulation in transport, 4.5 + +x +3 + +cm in lateral expansion, about +1 cm +thick, dirty white in color. The ZMA Por. 13446 specimen ( +Fig. 17a +) from Aqaba is small. It has a conical, transparent-white cormus with faint purple tinge, consisting of loosely, occasionally more tightly, anastomosed tubules, leading to a prominent single water-collecting tube ending in a wide oscule. + + +Aquiferous system. +Asconoid. + + +Skeleton +. ( +Figs 16b +, +17b +) Tubuli walls with one to two spicule layers, rather dense in preserved condition. + + +Spicules. +( +Figs 16c +, +17c +) Triactines only, neither specimen contained clearly identifiable trichoxeas as reported for some specimens in the +type +series. + + + +FIGURE 16. + +Clathrina rowi +Voigt +et al. +2017 + +, RMNH Por. 10002, Saudi Red Sea, Jeddah, field nr. JED209, a, in situ on the reefs (photo N.J. de Voogd), b, light microscopic view of the cormus, c, SEM image of the spicules. + + + + +FIGURE 17. + +Clathrina rowi +Voigt +et al. +2017 + +, ZMA Por. 13446, from Israel Red Sea, Aqaba, a, in situ in cave, b, light microscopic view of the cormus, c, SEM image of the spicules. + + + +Triactines with thin cylindroconical actines, endings mucronate to shortly pointed, occasionally slightly sagittal, size range limited, in RMNH Por. 10002 it is 68– +124 +–151 x 7.5– +9.3 +–11 µm, in ZMA Por. 13446 it is 48– +84 +–102 +x 5 +– +7.4 +–9 µm. + + + + +Distribution and ecology +. Saudi Arabian +Red Sea +, Israelian +Gulf +of Aqaba, on reefs. + + + + +Remarks. +The molecular sequence of the Jeddah specimen grouped with Voigt +et al. +’s + +C. rowi + +specimens (cf. +Fig. 2A +); no sequence for the Aqaba specimen was obtained. For that reason we present separate morphological data for the two available specimens. The shape of the cormus of the Jeddah specimen with the longer wider tubuli combined with a fine network of thinner tubuli is the same as in Voigt +et al. +’s +type +series. However, the shape (cylindroconical) and the size (up to 151 µm) of the triactines of the Jeddah specimen differ from the triactines of the +type +series, which has actines up to 103 µm long as described by Voigt +et al +. The Aqaba specimen has a comparable spicule size as the +type +series. + + +Sequence data for specimens assigned to + +C. rowi + +by + +Voigt +et al. +2017 + +were not strongly separated from sequences we found in specimens which we assigned to + +Clathrina luteoculcitella +Wörheide & Hooper, 1999 + +(cf. +Fig. 2A +). A larger clade with high bootstrap value unites our specimen and + +Voigt +et al. +’s (2017) + +specimens of + +C. rowi +, + +with Indonesian and Australian specimens of + +C. luteoculcitella + +as well as with +Rodrigues +specimens assigned below to + +C. luteoculcitella + +. In a separate analysis, a trimmed alignment with length 395 sites of both species comprising Australian (downloaded from the Sponge Barcode Project), Indonesian, +Red Sea +and +Oman +specimens of + +C. luteoculcitella + +, together 8 sequences, and 10 +Red Sea +sequences of + +C. rowi + +(most donated by Oliver Voigt, but including one of ours, RMNH 10002), showed nine non-conserved sites. Four of these sites showed a neat separation between C. + +luteoculcitella + +and + +C. rowi + +, the other 5 sites showed single specimen differences or a mixed set of differences. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC56A515FF678892FCC8FE56.xml b/data/38/6C/C6/386CC616DC56A515FF678892FCC8FE56.xml new file mode 100644 index 00000000000..dafa7875277 --- /dev/null +++ b/data/38/6C/C6/386CC616DC56A515FF678892FCC8FE56.xml @@ -0,0 +1,88 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + +Genus + +Clathrina +Gray, 1867 +sensu Klautau +et al. +2013 + + + + + + + +Remarks. +The species of the former large genus + +Clathrina + +have been subdivided by Klautau +et al. +2013 into distinct genera. The restricted genus + +Clathrina + +unites the species with asconoid tubuli anastomosed into loosely organized or more tightly anastomosed cormi with spiculation consisting exclusively of small triactines. We obtained a considerable number of partial 28SrRNA sequences to assist us in classifying the collected members of this still very large genus. We combined our sequences with our Indonesian, Oliver Voigt’s (2017), Sponge Barcode Project and GenBank + +Clathrina + +sequences in an analysis the results of which are given in the phylogenetic tree of +Fig. 2A +. See above for further comments on the results. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC56A517FF678A28FB25FA94.xml b/data/38/6C/C6/386CC616DC56A517FF678A28FB25FA94.xml new file mode 100644 index 00000000000..14d1eb75d71 --- /dev/null +++ b/data/38/6C/C6/386CC616DC56A517FF678A28FB25FA94.xml @@ -0,0 +1,318 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Clathrina sinusarabica +Klautau & Valentine, 2003 + + + + + +Figures 14a–d +, +15a–d + + + + + + +Clathrina coriacea + +; + +Row 1909 +: 184 + +(not: +Montagu 1814 +). + + + + + +Clathrina sinusarabica + +Klautau & Valentine, 2003 +: 45 + + +, fig. 37; + + +Voigt +et al. +2017 + +: 12 + +, fig. 7. +Material examined. +RMNH Por. 10003, Saudi Arabia, Jeddah, near Thuwal, Tahlah, 22.25725°N 38.880917°E, scuba, coll. N.J. de Voogd, field nr. THU14/JED 210, +13 November 2014 +; ZMA Por. 13414, Israel, Schuhmacher’s Pinnacle, Gulf of Aqaba, depth +6 m +, scuba, coll. M. Wunsch, field nr. AQ11, +1 July 1998 +; ZMA Por. 13476, Israel, pillar container port, Gulf of Aqaba, depth +5 m +, scuba, coll. M. Wunsch, field nr. AQ61, +5 July 1998 +. + + + + + +FIGURE 14. + +Clathrina sinusarabica +Klautau & Valentine, 2003 + +, a, RMNH Por. 10003, from the Saudi Arabian Red Sea, Jeddah (field nr. JED210), in situ on the reefs of Jeddah, a1, detailed view of water collecting tubes of the same (photos N.J. de Voogd), b, ZMA Por. 13414, at Aqaba, in situ on Schuhmacher’s Pinnacle, c, ZMA Por. 13476, at Aqaba’s container port (photos M. Wunsch). + + + + +Description. +Cushion of loosely anastomosed semi-transparent white tubuli ( +Figs 14a–c +) of +0.5–1.2 mm +diameter. Water collecting tubes ( +Fig. 14a +1 +) are common at the upper and lateral sides, but are less prominent in the Aqaba specimens ( +Figs 14b–c +). Preserved material is now fragmented and has pinkish color in alcohol. Size of the entire Jeddah specimen is 5 + +x 3 x +2 + +cm, the Aqaba specimens are slightly smaller. + + + +FIGURE 15. + +Clathrina sinusarabica +Klautau & Valentine, 2003 + +, a, light microscopic view of part of the cormus and tubuli of RMNH Por. 10003 from Jeddah, b–d, SEM images of spicules, b, of Jeddah specimen RMNH Por. 10003, c, of Aqaba specimen ZMA Por. 13414, d, of Aqaba specimen ZMA Por. 13476. + + + +Aquiferous system. +Asconoid. + + +Skeleton. +( +Fig. 15a +) Tubule walls thin, with single layer of spicules. + + +Spicules. +( +Figs 15b–d +) Equiradiate equiangular triactines with thin cylindroconical actines ending in pointed apices, 78–214 x 7.5–17.5 µm (n=75). + +The spicules sizes of the three specimens are: + +RMNH Por. 10003: 83– +164.4 +–194 x 7.5– +9.04 +–11 µm + + +ZMA Por. 13414: 107– +167 +–214 +x 9 +– +13.4 +–17.5 µm + + +ZMA Por. 13476: 78– +132 +–162 +x 9 +– +11.2 +–14.5 µm. + + + + +Distribution and ecology. +Saudi Arabia +, Jeddah, on reefs; if correctly identified it occurs in the Sudanese +Red Sea +, Agig, and the Israelian part of the +Gulf +of Aqaba, on reefs, depth + +5– +6 m + +. + + + + +Remarks. +The +type +of + +Clathrina sinusarabica +Klautau & Valentine, 2003 + +resembles our specimens in habitus and color, but the actines of its spicules are significantly shorter, 72–103 x 8.4 µm (according to +Klautau & Valentine 2003 +). We base ourselves for the identification on + +Voigt +et al. +’s (2017) + +description, which gives actines of 50–166 +x 8–18 +µm. The partial 28S sequence obtained for the Jeddah specimen conforms to Voigt’s molecular data (cf. +Fig. 2A +). The Jeddah specimen was sequenced, the Aqaba specimens were not. The Aqaba specimens appear to be morphologically similar, so we assume they are members of + +C. sinusarabica + +, but we gave separate measurements of the spicules of the three specimens, just in case. + + + +Morphologically, the present specimens resemble +Rodrigues +and +Seychelles +material described below as + +Clathrina rodriguesensis + + +sp.nov. + +, having firm whitish tubuli and robust triactines, but molecular data do not support this similarity (cf. +Fig. 2A +). + + + +The present specimens show also considerable resemblance to the Indonesian species + +Clathrina sororcula +Van Soest & De Voogd, 2015 + +, which has loosely anastomosed semi-transparent white tubes, cylindrical triactines of the same average length. Differences are the presence of several water-collecting tubes (raised oscules, absent in + +C. sororcula + +) and the greater size of the actines of the spicules. +No +molecular sequence data for + +C. sororcula + +could be obtained. + + + + + +Clathrina rowi + +Voigt +et al. +, 2017 + + +, + +Clathrina luteoculcitella +Wörheide & Hooper, 1999 + +and + +Clathrina chrysea +Borojević & Klautau, 2000 +sensu Van Soest & De Voogd 2015 + +are closely related in a molecular sense (cf. +Fig. 2A +). The New Caledonian +type +material of the latter was yellow, but life color of the Indonesian material was unknown. The color in alcohol is transparent-white like the present specimen. Spicule sizes match reasonably (75–144 +x 7–11 +µm), but actines are more conical. + +C. rowi + +and + +C. luteoculcitella + +are treated below. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC5BA51BFF67899EFE23FE6C.xml b/data/38/6C/C6/386CC616DC5BA51BFF67899EFE23FE6C.xml new file mode 100644 index 00000000000..6513716bdd6 --- /dev/null +++ b/data/38/6C/C6/386CC616DC5BA51BFF67899EFE23FE6C.xml @@ -0,0 +1,364 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Clathrina luteoculcitella +Wörheide & Hooper, 1999 + + + + + +Figures 18a–f +, +19a–e +, +20a–e + + + + + + +Clathrina luteoculcitella + +Wörheide & Hooper, 1999 +: 868 + + +, figs 5A–E + + + + +Clathrina +aff. +luteoculcitella + +; Van Soest & De Voogd 2015: 13, figs 6a–d. + + + + +Material examined. +RMNH +Por. 11623, +Mauritius +, +Rodrigues +, Passe Baladirou, +19.6683°S +63.46307°E +, depth +12 m +, scuba, coll. N.J. de Voogd, field nr. ROG024, +16 October 2016 +; +RMNH +Por. 11641, +Mauritius +, +Rodrigues +, Mourouk Ebony, Castel Rock, +19.76203°S +63.46273°E +, depth +10 m +, scuba, coll. N.J. de Voogd, field nr. ROG044, +17 October 2016 +; +RMNH +Por. 11659, +Mauritius +, +Rodrigues +, Mourouk Ebony, Castel Rock, +19.76203°S +63.46273°E +, depth +10 m +, scuba, coll. N.J. de Voogd, field nr. ROG063, +17 October 2016 +; +RMNH +Por. 11686, +Mauritius +, +Rodrigues +, Passe Baladirou, +19.6683°S +63.46307°E +, depth +12 m +, scuba, coll. N.J. de Voogd, field nr. ROG094, +18 October 2016 +; +RMNH +Por. 11687, +Mauritius +, +Rodrigues +, Mourouk Ebony, Castel Rock, +19.7648°S +63.4626°E +, depth +12 m +, scuba, coll. N.J. de Voogd, field nr. ROG101, +19 October 2016 +; +RMNH +Por. 11703, +Mauritius +, +Rodrigues +, Passe Saint François, +19.69893°S +63.5005°E +, depth +15 m +, scuba, coll. N.J. de Voogd, field nr. ROG117, +20 October 2016 +; +ZMA +Por. 17438, +Oman +, + +Muscat + +, Ras al Khayran, on rocks, +23.75°N +58.75°E +, (depth not recorded, but shallow), scuba, coll. O. Eerland, field nr. 02/IO/ +DEC08 +/OE/006, +6 December 2002 +; +ZMA +Por. 10223b, +Seychelles +, +Mahé +, NE coast, Cap Maçons and Anse de Forbans, +4.7667°S +55.5167°E +, depth +0–6 m +, snorkeling, coll. R.W.M. van Soest, field nr. +NIOP-E +stat. 612, +12 December 1992 +. + + + + +Description. +Cushion-shaped masses of tightly anastomed tubuli ( +Figs 18a–e +). Tubuli thin, +0.2–0.4 mm +in diameter. Numerous prominent oscules much wider than individual tubuli are visible on the upper side on in situ images (e.g. +Fig. 18a +). Color beige or orange-brown in situ, dirty white or pale beige ‘on deck’, ( +Fig. 18f +), pale beige in preserved condition. Consistency soft. Sizes up to +6 x 3 x +3 cm +, individual tubuli +0.2–0.3 mm +in diameter. The specimen from +Oman +had white live color, the +Seychelles +specimen was of unknown life color; both are pale beige ( +Fig. 20a +) in preserved condition. + + +Aquiferous system. +Asconoid. + + +Skeleton. +( +Figs 19a–b +, +20b,d +) Thin tubules with the walls single-spicule layered, not very dense. Spaces between the tubuli small, 0.1–0.5 µm. + + +Spicules. +( +Figs 19c–e +, +20c,e +) Triactines equiangular equiradiate, with small conical actines; some broken trichoxeas ( +Fig. 19d +). + + +Measurements of the actines of the triactines in three of the specimens from +Rodrigues +show a very limited variation: + + +RMNH Por. 11641: 69– +99 x +6.5–9.5 µm + + +RMNH Por. 11659: 72– +94 x 6–9 +µm + + +RMNH Por. 11687: 74– +93 x 6 +–9.5 µm + + +Overall, sizes are 69– +99 x 6 +–9.5 µm (n= 50). + +Few broken trichoxeas are found in one of the specimens. + +Triactines of the +Oman +specimen ( +Figs 20c +) are slightly larger, 72– +95.6 +–108 x 6.5– +9.4 +–12 µm (n=25); those of the +Seychelles +specimen ( +Fig. 20e +) are similar to the +Rodrigues +specimens: 71– +84 +– +96 x 7 +– +8.6 +–9.5 µm (n= 25). + + + + +Distribution and ecology. +Rodrigues +, +Oman +, +Australia +, +Indonesia +, on reefs at +0–15 m +depth. + + + + +Remarks. +The identification of the +Rodrigues +specimens with + +C. luteoculcitella + +is based on morphological and molecular characters. The species is distinct by its cushion-shaped mass of tightly meshed tubuli in combination with prominent oscules and small conical-actined triactines. Partial 28S sequence data point towards close relationship with Indonesian specimen ZMA Por. 0 8657 assigned to + +Clathrina luteoculcitella + +(cf. Van Soest & De Voogd 2015) and the Northeast Australian +holotype +of the species in the Sponge Barcode Project database. Together they form a sisterclade to a clade containing specimens of + +C. rowi + +(see +Fig. 2A +). + +Clathrina rowi + +is morphologically distinct from + +C. luteoculcitella + +as the cormus is more loosely organized and has different color. As reported above, the two show small but consistent molecular differences. + + +Likely members of + +C. luteoculcitella + +from +Oman +and the +Seychelles +have also a tightly meshed cormus and small spicules. The sequence of the +Oman +specimen matches closely with those of +Rodrigues +and Indonesian specimens of that species. However, the in situ color was noted as white, so some doubt is in order. The +Seychelles +specimen was very small and no sequence could be obtained, but what information we obtained makes membership of this species likely. We provide separate illustrations of the various specimens to support our conclusion that all are assumed to be conspecific. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC5FA500FF678892FE2AF946.xml b/data/38/6C/C6/386CC616DC5FA500FF678892FE2AF946.xml new file mode 100644 index 00000000000..76b11669ebb --- /dev/null +++ b/data/38/6C/C6/386CC616DC5FA500FF678892FE2AF946.xml @@ -0,0 +1,523 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Clathrina rodriguesensis + +sp.nov. + + + + +Figures 24a–e +, +25a–g +, +26a–d +, +27a–d + + + + + + +Material +examined. + +Holotype +, +RMNH +Por. 11694, +Mauritius +, +Rodrigues +, +Mourouk Ebony +, +Castel Rock +, +19.7648°S +63.4626°E +, depth + +12 m + +, scuba, coll. +N.J. de Voogd +, field nr. ROG108, + +19 October 2016 + +. + + + + +FIGURE 21. + +Clathrina rodriguesensis + + +sp.nov. + +, holotype RMNH Por. 11694, from Rodrigues, a, in situ (photo N.J. de Voogd), b, on deck (scale bar = 1 cm), c, preserved (scale bar = 1 cm), d, light microscopic image of the cormus, e, SEM images of the spicules. + + + + +FIGURE 22. + +Clathrina rodriguesensis + + +sp.nov. + +, paratypes from Rodrigues, a–d, RMNH Por. 11662 (ROG025), a, in situ on the reefs (photo N.J. de Voogd), b, detail of a, c, on deck photo of the same, (photo N.J. de Voogd) d, light microscopic image of part of the cormus of the same, e–g, RMNH Por. 11662 (ROG069), e, on deck photo, f, preserved specimen of the same, g, SEM images of the spicules of the same. + + + + +FIGURE 23. + +Clathrina rodriguesensis + + +sp.nov. + +, paratype RMNH Por. 11670 from Rodrigues, a, habitus in situ (photo N.J. de Voogd), b, habitus on deck, c, light microscopic images of the tubuli network, d, SEM images of the spicules. + + + + +FIGURE 24. + +Clathrina rodriguesensis + + +sp.nov. + +, specimens from the Seychelles, a, habitus of ZMA Por. 11282, preserved specimen (scale bar = 1 cm), b, light microscopic image of skeleton, c, SEM images of spicules, d, ditto of ZMA Por. 12096. + + + + +Paratypes +, +RMNH +Por. +11624, +Mauritius +, +Rodrigues +, +Passe Baladirou +, +19.6683°S +63.46307°E +, depth + +12 m + +, scuba, coll. +N.J. de Voogd +, field nr. ROG025, + +16 October 2016 + + +; + +RMNH +Por. +11662, +Mauritius +, +Rodrigues +, +Passe Baladirou +, +19.6683°S +63.46307°E +, depth + +12 m + +, scuba, coll. +N.J. de Voogd +, field nr. ROG069, + +18 October 2016 + + +; + +RMNH +Por. +11670, +Mauritius +, +Rodrigues +, +Passe Baladirou +, +19.6683°S +63.46307°E +, depth + +12 m + +, scuba, coll. +N.J. de Voogd +, field nr. ROG077, + +18 October 2016 + + +; + +RMNH +Por. +11671, +Mauritius +, +Rodrigues +, +Passe Baladirou +, +19.6683°S +63.46307°E +, depth + +12 m + +, scuba, coll. +N.J. de Voogd +, field nr. ROG078, + +18 October 2016 + + +; + +RMNH +Por. +11705, +Mauritius +, +Rodrigues +, +Passe Baladirou +, +19.6683°S +63.46307°E +, depth + +8 m + +, scuba, coll. +N.J. de Voogd +, field nr. ROG119, + +20 October 2016 + + +; + +RMNH +Por. +11710, +Mauritius +, +Rodrigues +, +Passe Saint François +, +19.69893°S +63.5005°E +, depth + +15 m + +, scuba, coll. +N.J. de Voogd +, field nr. ROG124, + +20 October 2016 + + +. + + + +Additional specimens. +ZMA +Por. +11282, +Seychelles +, +Amirantes +, +Desroches Atoll +, SW rim, +5.7167°S +53.6167°E +, depth + +5–30 m + +, scuba, coll. +M.J. de Kluijver +, field nr + +. NIOP-E stat. 774/01, +30 December 1992 +; + +ZMA +Por. +12096, +Seychelles +, +Amirantes +, +St. François Atoll +, +Île Bijoutier +, +7.0833°S +52.7333°E +, reef, outer slope, depth + +6–18 m + +, scuba, coll. +R.W.M. van Soest +, field nr + +. NIOP-E stat. 792/12, +5 January 1993 +. + + + + +Description. +In situ, the species forms a massively encrusting cormus ( +Figs 21a–d +, +22a–b +) consisting of relatively wide tubuli (approximately up to +2–3 mm +in diameter), which are nevertheless closely anastomosed, showing little differentiation in tubule-width. The cormus may be also flatly encrusting over a larger area ( +Fig. 23a +) with loosely anastomosing tubuli showing a tendency to be arranged ladder-like, with longitudinal main tubuli and interconnecting secondary thinner tubuli. The main tubuli frequently end in an oscule, often slightly erected above the cormus ( +Figs 22a–b +). Lateral size considerable, + +20 x +15 + +cm or more, thickness +1–4 cm +. Color white with blueish or greyish tinges in situ, white or pink ‘on deck’ ( +Figs 21b +, +22c,e +, +23b +), in preservation they become pale beige ( +Figs 21c +, +22f +: +Rodrigues +specimens) or brown ( +Fig. 24a +: +Seychelles +specimens). The latter have possibly become brown by exposure to algae or other sponges, as their in situ color was noted as blueish white. Size of preserved fragments up to 10 x 5 + +x +4 + +cm. Consistency firm. + + +Aquiferous system. +Asconoid. + + +Skeleton. +Tubule walls multi-layered, densely crowded in most specimens ( +Figs 21d +, +22d +, +23c +), but less dense in one of the +Seychelles +specimens ( +Fig. 24b +). + + +Spicules. +( +Figs 21e +, + +22g + +, +23d +, +24c–d +). Triactines only, but occasional fragments of trichoxea-like spicules were observed (not shown). + + +Triactines, robust, with conical actines, measuring 97– +169 +–225 +x 11 +– +18.2 +–22 µm in the Rodrigues specimens. The two Seychelles specimens which we believe to belong to this species have actines respectively 93– +159 +–198 +x 11 +– +17.4 +–21 µm (ZMA Por. 11282) and 111– +164 +–204 +x 13 +– +17.8 +–21 µm (ZMA Por. 12096) ( +Figs 24c–d +). The actines in all these specimens are conical + + + + +Distribution and ecology. +Rodrigues +, +Seychelles +, on reefs, +5–30 m +depth. + + + + +Etymology. +The name refers to the +type +locality, the island of +Rodrigues +, east of +Mauritius +. + + + + +Remarks. +We provide ample illustrations of this new species to demonstrate the habitus variability. Spicules are closely similar in all above-mentioned specimens. + + +Partial 28S sequences of seven specimens collected at +Rodrigues +and two +Seychelles +specimens grouped in a separate clade (cf. +Fig. 2A +) at high bootstrap value, apparently not closely related to the other +Western +Indian Ocean + +Clathrina + +. + + +Australian and Indonesian + +Clathrina heronensis +Wörheide & Hooper, 1999 + +is close in color and spicule size and shape, but its habitus is flatly encrusting and it has thinner tubuli ( +1 mm +) than the present material. An Indonesian specimen identified as + +C. heronensis + +was sequenced and found to share a clade with lower bootstrap value with the present material in the molecular tree of +Fig. 2A. A +separate analysis of the sequences of both species in a trimmed alignment with length of 395 sites showed a difference of eight sites between + +C. heronensis + +and + +C. rodriguesensis + + +sp.nov +. + + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC64A527FF678892FD03F852.xml b/data/38/6C/C6/386CC616DC64A527FF678892FD03F852.xml new file mode 100644 index 00000000000..34ac330df19 --- /dev/null +++ b/data/38/6C/C6/386CC616DC64A527FF678892FD03F852.xml @@ -0,0 +1,381 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Arturia sueziana +( +Klautau & Valentine, 2003 +) + + + + + +Figures 4a–f + + + + + + +Clathrina canariensis +var. +compacta + +; + +Row 1909 +: 184 + +(not: +Schuffner, 1877 +). + + + + + +Clathrina sueziana + +Klautau & Valentine, 2003 +: 43 + + +, fig. 35. + + + + + +Arthuria sueziana + +; + + +Voigt +et al. +2017 + +: 15 + +, figs 9a–h. + + + + + + + +Material +examined. + +RMNH +Por. 9537, +Saudi Arabia +, +Jeddah +, near +Thuwal +, +Al Bilut +( +Rose Reef +), +22.309861°N +38.886472°E +, depth + +12 m + +, scuba, coll. +N.J. de Voogd +, field nr. THU03/JED022, + +7 November 2014 + + +; + +RMNH +Por. 10112, +Maldives +, +Faafu Atoll +, +Free Climbing +, +3.066583°N +72.923028°E +, depth + +15 m + +, scuba, coll. +N.J. de Voogd +, field nr. +MAD06 +/MAS067, + +18 February 2015 + + +. + + + + +Description. +Relatively massive, rounded to conical cormi of tightly anastomosed tubuli, converging at the upper surface to a few wide, tapering oscular (water-collecting) tubes ( +Figs 4a–c +). Overall size is up to +3 x +1.5 x +1.5 cm +, tubuli diameters +0.2–0.5 mm +, water-collecting tubes up to +8 mm +in diameter. Color pale yellow or dirty white. + + +Aquiferous system. +Asconoid. + + +Skeleton. +( +Figs 4d +) The tubule wall has two or more layers of overlapping triactines and tetractines, the latter with the apical actines protruding in the tubar lumen. The ratio of triactines vs. tetractines was 7: +1 in +RMNH 9537 and 7.5: +1 in +RMNH 10112, a clear predominance of triactines. + + +Spicules. +( +Figs 4e–f +) Triactines and tetractines; trichoxeas were observed in a very low frequency in all samples, invariably broken. + + +Triactines ( +Figs 4e +) predominantly equiradiate and equiangular, but a few are sagittal with paired actines wingshaped. Actines conical, actine lengths in the various specimens: + + +RMNH Por. 9537: 96– +128.8 +–146 x 8.5– +10.5 +–14.5 µm (paired and unpaired actines of sagittal triactines of approximately same length). + + + +RMNH +Por. 10112: 48– +111 +–153 + +x 6 + +– +11.8 +–15 µm (ditto). + + + +Tetractines ( +Fig. 4f +) with basal triradiate system predominantly equiradiate, occasionally sagittal, with apical actines smooth, thinner, but up to the same length of the actines of the basal triradiate system. Basal actines conical, actine sizes in the various specimens: + + +RMNH Por. 9537: 36– +119.4 +–147 +x 4 +– +10.7 +–14 µm, apical actines 54– +104.4 +–164 +x 4 +– +4.9 +–7 µm. + + +RMNH Por. 10112: 64– +115 +–156 +x 6 +– +10.2 +–13 µm, apical actines 32– +84 +–153 +x 4 +– +5.7 +–8.5 µm. + + + + +Distribution and ecology. +Red Sea +( +Suez +; Thuwal Reefs, near Jeddah), +Maldives +, in reef localities under overhangs. + + + + +Remarks. +This is the first time the species has been recorded from outside the +Red Sea +. The habitus and spicular characters of the Jeddah and +Maldives +specimens in our collection are so close that conspecificity seems obvious. There are some spicule size differences with the +Suez +holotype +(tetractines are only up to 98 µm, apical actines of the tetractines are only up to 63 µm). In + +Voigt +et al. +’s (2017) + +specimens there was a clear presence of trichoxeas (also mentioned in the +holotype +, quite rare in the present material). However, trichoxeas are notoriously variable in +Clathrinidae +, and the habitus and overall characters match with all three records. + + +We obtained a partial 28S rRNA sequence for the +Maldives +specimen (sequencing of our +Red Sea +specimen failed). The +Maldives +sequence ended up in the same clade together with three +Red Sea +sequences from + +Voigt +et al. +(2017) + +in a high bootstrap support (cf. +Fig. 2C +). Nevertheless, the identical +Red Sea +sequences together differed substantially from the +Maldives +sequence (in more than 10 sites), indicating a possible specific difference, which may become evident when more studies of +Western +Indian Ocean localities have been made. + + + + + +Arturia darwinii +( +Haeckel, 1872 +) + +was reported from Zanzibar by +Jenkin (1908) +as + +Clathrina + +. It was described as bright lemon-yellow in color and the tri-and tetractines had basal actines 60–120 +x 12–16 +µm, with the apical actines of the tetractines having the same length but thinner (8 µm). These measurements overlap with the above given data on + +A. sueziana + +. The species is also reported from the Mozambique Channel by +Barnes & Bell (2002) +, but no description was given. The type locality of + +A. darwinii + +is Java, Indonesia (cf. Van Soest & De Voogd 2015), but Haeckel also reported specimens from the Red Sea. The distinction between + +A. darwinii + +and + +A. sueziana + +remains to be further established. + + +All the above presented discrepancies with the +holotype +of + +A. sueziana + +support Klautau & Valentine’s (2003) statement that + +A. sueziana + +is a complex of species. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC67A524FF6789B8FCEFFB03.xml b/data/38/6C/C6/386CC616DC67A524FF6789B8FCEFFB03.xml new file mode 100644 index 00000000000..5cd921c2ff1 --- /dev/null +++ b/data/38/6C/C6/386CC616DC67A524FF6789B8FCEFFB03.xml @@ -0,0 +1,196 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + +Family + +Clathrinidae +Minchin, 1900 + + + + + + + +Remarks. +Since the Systema Porifera classification of the order +Clathrinida +(see + +Borojević +et al. +2002a + +), substantial changes of the contents of the family +Clathrinidae +have been proposed (Klautau +et al. +2013) and elaborated (Klautau +et al. +2016). The genus + +Clathrina +Gray, 1867 + +has been subdivided into five distinct genera, + +Arturia + +Azevedo +et al., +2017 + + +(pro + +Arthuria +Klautau +et al +., 2013 + +), + +Borojevia +Klautau +et al. +, 2013 + +, +Ernstia +Klautau +et al. +, 2013, + +Brattegardia +Klautau +et al. +, 2013 + +, and + +Clathrina + +s.s +.. The only other genus of the family recognized in the Systema Porifera, genus + +Guancha +Miklucho-Maclay, 1868 + +, has been subsumed into + +Clathrina + +s.s. +, because its +type +species + +Guancha blanca +Miklucho-Maclay, 1868 + +has been transferred to + +Clathrina +sensu Klautau +et al. +, 2013 + +. One former + +Guancha + +species, + +G. tetela +Borojević & Peixinho, 1976 + +was recently reassigned to a new genus, + +Nicola +Condór-Luján & Klautau, 2016 + +. The classification is still in a flux, as it was recently revealed that the name + +Arthuria + +was preoccupied by two Mollusca genera (Polyplacophora and +Pulmonata +). It has just now been replaced by + +Arturia +, + +but it is still complicated by our discovery (see below) that + +Arturia + +is probably not a monophyletic genus. + + +The family contents are also possibly overlapping with other families of the order +Clathrinida +, awaiting an overhaul based on a phylogenetic analysis of molecular sequence data. We will here follow the classification as presented in Klautau +et al. +2013, with above listed recognized genera presented in alphabetical order ( + +Brattegardia + +excepted as it was not represented in our material). + + +Below we will use the word ‘tubuli’ to describe the anastomosed ascon tubes of +Clathrinidae +species to avoid confusion with the tubes of tubular habitus in some species with a pseudoatrium. We maintain the term ‘watercollecting tubes’ for those wider tubuli leading to oscules. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC67A524FF678CE9FECDF877.xml b/data/38/6C/C6/386CC616DC67A524FF678CE9FECDF877.xml new file mode 100644 index 00000000000..8d3a163a42b --- /dev/null +++ b/data/38/6C/C6/386CC616DC67A524FF678CE9FECDF877.xml @@ -0,0 +1,251 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + +Genus + +Arturia + +Azevedo +et al. +, 2017 + + + + + + + + +Remarks. +Our Calcinea phylogeny ( +Figs 2, 2A, 2C +) shows a peculiar discrepancy in the affiliation of the two species of + +Arturia + +we found in our collection of Calcarea from the +Western +Indian Ocean. + +A. sueziana +( +Klautau & Valentine, 2003 +) + +is grouped on its own in +Figs 2 and 2C +outside any of the Calcinean genus and family clades, whereas + +A. adusta +( +Wörheide & Hooper, 1999 +) + +ended up close to the main group of + +Clathrina + +species. We investigated which of the two species is closest to the +type +species of + +Arturia + +, i.e. + +A. hirsuta +( +Klautau & Valentine, 2003 +) + +, by downloading the available GenBank 18S sequences of + +Arturia + +species, because apart from + +Voigt +et al. +’s (2017) + +28S rRNA sequences and our own, there are no other + +Arturia + +sequences of that gene in GenBank. The 18S sequences of the +type +species (accession numbers +KC843431 +& +KC985143 +), of + +A. sueziana + +( +KY366410 +), of + +Clathrina adusta + +(AM +180962 +), of two additional unnamed + +Arturia + +species ( +KC985141 +& +KC985142 +), of +Ernstia tetractina +, of + +Clathrina sinusarabica +Klautau & Valentine, 2003 + +( +KY366407 +), and of + +Leucetta floridana +Haeckel, 1872 + +( +KC843456 +) were analyzed with the MEGA package.The result (not shown) clearly confirmed that + +A. sueziana + +is close to the +type +species + +A. hirsuta + +and the two unnamed + +Arturia + +, near + +Leucetta floridana +, + +and that + +Clathrina adusta + +did not group with these, but ended up separately and nearer to + +Clathrina sinusarabica + +and +Ernstia tetractina +. In our +Fig. 2A +it is demonstrated that + +Arturia adusta + +is joined by the Indonesian + +Arturia tubuloreticulosa +Van Soest & De Voogd, 2015 + +and + +Arturia angusta +(Van Soest & De Voogd, 2015) + +(transferred here, but originally as + +Ascaltis + +). We are not proposing a new genus for this second + +Arturia + +group, but we confirm + +Voigt +et al. +’s (2017) + +suggestion that the + +Ernstia - +Arturia + +relationships need to be analyzed further, not only molecularly, but also morphologically. The morphological characters provided by Klautau +et al. +(2013) fail to give sufficient support for recognition of three + +Clathrina + +-like generic taxa with tetractines, +Ernstia +, + +Arturia + +s.s. +and ‘ + +Arturia + +’. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC69A510FF678D66FBB8FE49.xml b/data/38/6C/C6/386CC616DC69A510FF678D66FBB8FE49.xml new file mode 100644 index 00000000000..a7edac65d9f --- /dev/null +++ b/data/38/6C/C6/386CC616DC69A510FF678D66FBB8FE49.xml @@ -0,0 +1,653 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Borojevia tubulata + +sp.nov. + + + + +Figures 8a–c +, +9a–f +, +10a–h +, +11a–f + + + + + + +Material +examined. + +Holotype +, +RMNH +Por. 10158, +Maldives +, +Faafu Atoll +, +Wallstreet +, +3.119°N +72.979556°E +, depth + +12 m + +, scuba, coll. +N.J. de Voogd +, field nr. +MAD10 +/MAS119, + +20 February 2015 + +. + + + + +Paratype +, +RMNH +Por. 10113, +Maldives +, +Faafu Atoll +, +Free Climbing +, +3.066583°N +72.923028°E +, depth + +15 m + +, scuba, coll. +N.J. de Voogd +, field nr. +MAD06 +/MAS068, + +18 February 2015 + +. + + + + +Additional material, +ZMA +Por. 12435, +Seychelles +, +Amirantes +, +Desroches Atoll, SW +rim, outer reef slope, +5.7167°S +53.6167°E +, depth + +5–30 m + +, scuba, coll. +M.J. de Kluijver +, +NIOP-E +stat.nr. 774/04, + +30 December 1992 + + +. + + + + +Description. +Irregularly arranged, groups of tubular individuals, the walls of which consist of tightly anastomosed tubuli. In situ white ( +Figs 8a +, +10a +) or cream or yellow-white ( +Fig. 8b +) colored, on deck ( +Figs 8c +, +10b +) and preserved they are cream to pale beige ( +Figs 10c +, +11a +). Height of tubes up to about +3 cm +, width +0.5 cm +at the aperture and +1 cm +at the base, but individual tubes may be smaller and thinner. Tube apertures are about as wide as the (pseudo-)atrium or slightly narrower. In preservation the tubes collapse to form easily damaged soft and flabby fragments ( +Figs 8c +, +10b–c +, +11a +), which have their (pseudo-)atrium flattened to a narrow slit ( +Fig. 11b +). The tube walls are ‘punctate’ ( +Figs 9a +, +10d +) caused by regularly distributed pseudopores (cf. Dendy’s (1913) description of + +Ascaltis gardineri + +, as + +Leucosolenia + +), which give access to the densely crowded tubuli. + + +Aquiferous system. +Asconoid. + + + +FIGURE 8 +. + +Borojevia tubulata + + +sp.nov. + +, holotype RMNH Por. 10158, from the Maldives, a, habitus of one of the groups of tubes white-colored, b, ditto cream-colored (both sampled groups of tubes were included in a single preserved sample and were subsequently not separated and were together joined as the holotype), c, holotype photographed on deck after collection (scale bar mm) (photographs N.J. de Voogd). + + + + +FIGURE 9. + +Borojevia tubulata + + +sp.nov +. + +, holotype RMNH Por. 10158, from the Maldives, SEM images of sections and spicules, a, view of surface showing pseudopores and large triactines at the surface, b, cross section of tube wall, upper part outside, lower part pseudoatrium, c–f, SEM images of the spicules, c, large triactines from the outer surface, d, smaller triactines from the inner tubuli, d1, sagittal triactine, e, tetractines, f, detail of spined apical actine of tetractine. Please note that rows of spines are in line with the basal radiate system. + + + + +FIGURE 10. + +Borojevia tubulata + + +sp.nov. + +, paratype RMNH Por. 10113, from the Maldives, a, in situ white group of tubes (photo N.J. de Voogd), b, on deck fragmented groups of tubes (scale bar mm), c, preserved paratype (scale bar = 1 cm), d. light microscopic image of surface skeleton showing characteristic pattern of larger triactines, e–h, SEM images of spicules, e, large triactine of the outer surface, f, small triactines of the inner tubuli, g, tetractines, h, detail of spined apical actine of tetractine. + + + + +FIGURE 11 +. + +Borojevia tubulata + + +sp.nov. + +, ZMA Por. 12435, from the Seychelles (Amirantes region), a, preserved habitus of fragmented tubes (scale bar = 1 cm), b, cross section of flattened tube with slit-like flattened pseudoatrium, c–f, SEM images of spicules, c, large triactine of the surface, d, small triactine of the interior skeleton, e, tetractines, f, details of spined apical actines of the tetractines. + + + +Skeleton. +The pseudopores of the outer tube walls are strengthened by larger triactines, arranged in a distinct cortical pattern ( +Figs 9a +, +10d +), the skeleton of the walls of the tubuli are built by one-two layers of smaller triactines and tetractines, with the apical actines of the tetractines protruding into the lumina of the tubuli. The atrial sides of the tube walls ( +Fig. 9b +) have an irregular skeleton and do not exhibit a special arrangement of larger triactines as observed on the outer wall, which indicates that the atrium is in fact a pseudoatrium, as is characteristic of the genus + +Ascaltis + +according to the Systema Porifera ( + +Borojević +et al +. 2002a + +). See below for a further discussion. + + +Spicules. +( +Figs 9d–f +, +10e–h +, +11c–f +) Triactines in two size classes, tetractines with spined apical actines. The latter invariably have the spines in three distinct rows the position of which match the basal triadiate system. We did not observe the presence of tripods, but we presume the larger category of triactines is homologous. Because of slight discrepancies between the specimens, we provide separate images of the samples and measurements of the three samples: + + +Holotype RMNH Por. 10158: Larger triactines ( +Fig. 9c +) of the outer tube wall, equiradiate or very rarely sagittal, robust, with conical actines, which may slightly differ in length in the same spicule, actines 92– +133 +–189 +x 11 +– +13.4 +–16 µm. + + +Smaller triactines ( +Figs 9d,d +1 +), equiradiate ( +Figs 8d +), or rarely sagittal ( +Fig. 9d +1 +) with undulate paired actines, measuring 54– +63 +–111 +x 5 +– +6.3 +–7.5 µm. + + +Tetractines ( +Figs 9e–f +), with basal triradiate system usually equiradiate, but very occasionally there may be sagittal spicules, 51– +68 +– +96 x 6 +– +6.6 +–9 µm, apical actines ( +Fig. 9f +) 24– +37 +– +48 x +3.5– +4.4 +–5 µm. + + +Paratype RMNH Por. 10113: Larger triactines ( +Fig. 10e +) with conical actines, 129– +151 +–174 +x 14 +– +15.2 +–18 µm; one single sagittal triactine was observed in the slides. + + +Smaller triactines ( +Figs 10f +), with conical actines, 59– +72 +– +93 x 6 +– +7.2 +–10 µm. + + +Tetractines ( + +Figs +10g + +), with conical actines, those of the basal radiate system 48– +67 +– +78 x +4.5– +6.6 +–8 µm, apical actines with spines ( +Fig. 10h +), 35– +43 +– +58 x 4 +– +5.2 +–7 µm. + + +ZMA Por. 12435 ( +Figs 11c–f +): Larger triactines ( +Fig. 11c +), 102– +117.6 +–134 +x 11 +– +13.4 +–17 µm + + +Smaller triactines ( +Fig. 11d +), 51– +75.1 +– +94 x 6 +– +8.4 +–10 µm + + +Tetractines ( +Figs 11e +), 61– +76.3 +– +88 x 7 +– +8.6 +–10 µm, apical actines with spines ( +Figs 10f +), 40– +53.4 +– +74 x 6 +– +6.6 +–7µm. + + + + +Distribution and ecology. +Maldives +, +Seychelles +, under overhangs on coral reefs, depth + +5– +30 m + +. + + + + +Etymology. +Tubulatus (L.) means tube-shaped, referring to the habitus of the species. + + + + +Remarks +. The three samples show some discrepancies, which we consider to be infraspecific variability. The two +Maldives +samples have similar habitus, but show some color differentiation between distinctly white and more creamy or pale yellow. The +holotype +has a larger proportion (though still a clear minority) of sagittal tri- and tetractines than the +paratype +. The +Seychelles +specimen was noted to be yellow in color, and it lacks sagittal spicules entirely. The +Seychelles +specimen has smaller triactines than the +Maldives +and the distinction between larger and smaller spicules is less obvious. For this reason, we limited the +type +material to that of the +Maldives +only. However, we believe that the three samples are conspecific. + + +The species is assigned to the genus + +Borojevia + +despite the elaborate shape and presence of a pseudoatrium, and despite the absence of clear tripods among the triactines. In fact, we initially assigned the specimens to the genus + +Ascaltis + +, based on the habitus and skeletal structure and because a Western Indian Ocean species, + +Ascaltis gardineri +(Dendy, 1913) + +appeared to be close in skeletal characters. The major difference between that species and our specimens is the lobate, non-tubular habitus in the former. + + +Molecular sequence data (partial 28S, cf. +Fig. 2B +) were obtained for the +holotype +and the +Seychelles +material of + +Borojevia tubulata + + +sp.nov. + +Our phylogenetic analysis of Calcinean sequences, obtained from our own Western Indian Ocean samples, + +Voigt +et al. +’s (2017) + +samples (we were allowed to include a recent sequence of + +Borojevia + +sp. from the +Maldives +kindly sent to us by Oliver Voigt, which is likely a member of the present new species), and from GenBank, clearly showed that the present species is closely related to + +Borojevia aspina +( + +Klautau +et al +., 1994 + +) + +, + +Borojevia +aff. +aspina +sensu + +Voigt +et al +. 2017 + + +, + +B. cerebrum +( +Haeckel, 1872 +) + +, + +B. brasiliensis +( + +Solé-Cava +et al. +1991 + +) + +and a new + +Borojevia + +species decribed below, and was distant from + +Ascaltis reticulum +( +Schmidt, 1862 +) + +, the only + +Ascaltis + +for which molecular data are available. As Klautau +et al. +(2016) pointed out, we cannot be certain about the molecular affiliation of the genus + +Ascaltis + +yet, because there are no sequences available for the +type +species + +Ascaltis lamarcki +( +Haeckel, 1872 +) + +. We have chosen to follow the molecular signal and keep our species in the genus + +Borojevia + +, against the weight of morphological evidence for a possible membership of + +Ascaltis + +. + + +The new species differs from the above-described + +Borojevia voigti + + +sp.nov. + +in the presence of a pseudoatrium and the more prominent and consistent spination of the apical actines of the tetractines. + + +A further similar species appears to be + +Leucascus simplex +Dendy, 1892 + +, from + +South +Australia + +, reported also from Providence Island in the +Seychelles +by Dendy (1913). The +type +of that species has spined apical actines (cf. redescription of + +L. simplex +in + +Cavalcanti +et al. +2013 + + +), but it has not been verified for the Providence specimen. This differs from the present species also in habitus (massive, with only a slit-like atrial cavity). Below we describe a new species of + +Leucascus + +from Eastern + +South +Africa + +. Apart from a more elaborate shape, it is distinct by having a surface palisade of short diactines. The present species is not a likely +Leucascu +s, as in our phylogeny of +Fig. 2 +, + +Leucascus flavus +Cavalcanti + +et al,. +2009 is not at all closely related to + +Borojevia + +species. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC6AA528FF678892FDCBFB89.xml b/data/38/6C/C6/386CC616DC6AA528FF678892FDCBFB89.xml new file mode 100644 index 00000000000..da0d64f7c9a --- /dev/null +++ b/data/38/6C/C6/386CC616DC6AA528FF678892FDCBFB89.xml @@ -0,0 +1,331 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Arturia +(?) + + +adusta +( +Wörheide & Hooper, 1999 +) + + + + + +Figures 5a–e + + + + + + +Clathrina adusta + +Wörheide & Hooper, 1999 +: 865 + + +, figs 4D–H. + + + + +Ernstia +adusta + +; Klautau +et al. +2013: 12. + + + + + +Arthuria adusta + +; Voigt & Wörheide 2016: 61 + + + + +Clathrina +aff. +adusta + +; + + +Voigt +et al. +2017 + +: 5 + +, fig. 3. + + + + + + + +Material +examined. + +ZMA +Por. 10612, +Seychelles +, + +La Digue Island +, S + +coast, +4.3833°S +55.8333°E +, depth + +2–8 m + +, snorkling, coll. +R.W.M. van Soest +, field nr + +. NIOP-E stat. 735/ +32, 23 December +1992. + + + + +Description. +Cormus a small cushion ( +Fig. 5a +), about +1 x +0.7 cm +in lateral expansion, thickness +2–4 mm +. Life color is unknown, in alcohol it is orange-yellow. Structure compact, made up of tightly anastomosed thin tubuli. No visible oscules. Consistency soft. + + + +FIGURE 5. + +Arturia +(?) + + +adusta +(Wörheide & Hooper, 1999) + +, ZMA Por. 10612, from the Seychelles, La Digue island, a, preserved habitus (scale bar = 1 cm), b, light microscopic image of cormus showing tight anastomosis of tubuli, c–e, SEM images of the spicules, c, triactines, d, tetractines, e, detail of apical actine of tetractine. + + + +Aquiferous system. +Asconoid. + + +Skeleton. +( +Fig. 5b +) Wall of tubuli thin, consisting of one-two spicule layers with a prominence of triactines. The apical actines of the tetractines are protruding into the tubule lumina. + + +Spicules. +( +Figs 5c–e +) Triactines and tetractines, the latter present in clearly smaller numbers. No distinct trichoxeas were found. + + +Triactines ( +Figs 5c +) equiradiate and equiangular, with conical actines, some verging toward tripod-shape; actine sizes 48– +76 +–108 x 6.5– +8.7 +–12 µm. + + +Tetractines ( +Figs 5d +) of similar shape and size to the triactines, actines of the basal triradiate system 54– +73 +– +87 x +6.5– +7.6 +–9.5 µm; apical actines ( +Fig. 5e +) smooth, straight, sometimes with a slightly upturned apex, 39– +55 +– +78 x 3 +– +5.9 +–7.5 µm. + + + + +Distribution and ecology. +Egyptian Red Sea ( + +Voigt +et al. +2017 + +), +Seychelles +, NE +Australia +, on reefs in shallow depths. + + + + +Remarks. +We base our identification largely on the sequence we obtained for our species, which ended up in a clade together with + +Voigt +et al. +’s (2012) + +Australian sequence of + +Arturia adusta + +and + +Voigt +et al. +’s (2017) + +Red Sea + +Clathrina +aff. +adusta + +(see his fig. 3). Klautau +et al. +(2013) had earlier assigned + +Clathrina adusta + +to +Ernstia +. Voigt & Wörheide (2016) discovered that this species falls outside the +Ernstia +clade and suggested that it should go to + +Arturia + +. We confirm that + +C. adusta + +is not an +Ernstia +, but with + +Voigt +et al. +(2017) + +we agree that assignment of + +C. adusta + +to + +Arturia + +s.s. +is probably not correct, because + +Arturia sueziana + +and the +type +species of the genus + +Arturia + +, did not group in the same clade as + +C. adusta + +(see discussion above). + + +The present specimen resembles the type of +Wörheide & Hooper (1999) +, although the white color cannot be affirmed. In glutaraldehyde the color of the type apparently changed to dark brown. Actine sizes 90–142 +x 12–20 +µm, more robust than in the Seychelles specimen, but overlapping. + +Voigt +et al +.’s (2017) + +record from the Red Sea mentioned actine sizes of 66– +73 x 9–10 +µm, more similar to our specimen than to the type. The three sequences for these specimens differed only in a few sites (two between the type and the Seychelles specimen, three between the type and the Red Sea specimen). + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DC6BA52BFF678CA1FC3FF8AF.xml b/data/38/6C/C6/386CC616DC6BA52BFF678CA1FC3FF8AF.xml new file mode 100644 index 00000000000..a65b5ea626b --- /dev/null +++ b/data/38/6C/C6/386CC616DC6BA52BFF678CA1FC3FF8AF.xml @@ -0,0 +1,263 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Borojevia voigti + +sp. nov. + + + + +Figures 6a–d +, +7a–d + + + + + +Material examined. +Holotype +, +ZMA +Por. 13444, +Israel +, pillar container port, +Gulf +of Aqaba, depth + +5 m + +, scuba, coll. +M. Wunsch +, field nr. AQ + +65, 5 July + +1998. + + + + + +Description. +Cormus ( +Figs 6a,a +1 +) a greyish white cushion ( +Fig. 6a +1 +, arrow), brighter white in alcohol ( +Fig. 6a +), made up of tightly anastomosed thin tubuli. Oscules small, about +2 mm +diameter, flush with the surface. Size of entire specimen is 2.5 + +x 2 x +1 + +cm. + + +Aquiferous system. +Asconoid. + + +Skeleton. +( +Figs 6b–d +) Tubuli walls consist of one–two layers of triactines and tetractines. Apical actines of tetractines protruding into the tubar lumen ( +Fig. 6d +). + + +Spicules. +( +Figs 7a–d +) Triactines and tetractines, about equal in number. Some trichoxea-like spicules appear present in the spicule slides. + + +Triactines ( +Fig. 7a +) equiradiate and equiangular, with conical actines measuring 42– +89 +–117 +x 7 +– +8.7 +–11 µm. + + +Tetractines ( +Figs 7b–d +) shaped similarly and of approximate equal size. Apical actines straight, equal in length or longer than the actines of the basal triradiate system, tapering to a thin point ( +Fig. 7b +), occasionally entirely smooth ( +Fig. 7c +left), but usually provided with a few small spines ( +Figs 7c +right). Actines of the basal triradiate system 32– +61 +–105 +x 4 +– +6.8 +–10 µm, apical actines 24– +67 +–138 +x 3 +– +5.1 +–7 µm. + + +?Trichoxeas ( +Fig. 7d +), up to 300+ µm, quite thin (less than 0.5 µm in thickness). +Not +certainly proper as they are not visible in the sections. + + + + +Distribution and ecology. +Red Sea +, Aqaba, under overhangs in reef localities. + + + + +Etymology. +Named after Dr Oliver Voigt, München, for his excellent contributions to Calcarea systematics. + + + + +Remarks. +The present specimen resembles to some extent + +Voigt +et al. +’s (2017) + +description of + +Borojevia +aff. +aspina +( + +Klautau +et al. +, 1994 + +) + +. The trichoxea-like spicules are present in the spicule slide at a low frequency. In the surface section ( +Fig. 6c +) there are some thin long spicules, but they are indistinct and may not be proper to the sponge. Voigt +et al. +also observed that the trichoxeas are difficult to find in the slides. Voigt +et al. +did not observe spines on the apical actines of the tetractines, which is a distinct difference. In our new species the spines were very small and occasionally absent in our specimen ( +Figs 7c +left), thus we assume our and Voigt +et al. +’s specimens belong to different closely related species. Like Voigt +et al. +’s specimen ours has whitish color and it lacks distinct tripods. Since + +Borojevia aspina + +is a Brazilian species, the likelihood that a species living on reefs in the +Red Sea +is conspecific with the Brazilian population is judged to be quite small. + + + +FIGURE 6. + +Borojevia voigti + + +sp.nov +. + +, holotype ZMA Por. 13444, a, preserved holotype (scale bar = 1 cm), a1, small indistinct in situ image of holotype (arrow) growing in a hollow of a pillar in the Eilat container harbor, Israel (photo cut out from larger image made by M. Wunsch), b–d, SEM images of sections of the holotype, b, cross section, c, surface section, d, enlarged part of cross section showing protruding apical actines of tetractines. + + + +Borojević (1967) +described the Mediterranean species + +Clathrina cerebrum + +from Eastern South Africa (Natal coast). This combination is now assigned to + +Borojevia + +and restricted to the Mediterranean (cf. Klautau +et al. +2016). It is cushion-shaped like the new species, but it has tripods, making it unlikely to be the same species. + + +So far, no other species of + +Borojevia + +have been reported from the region, but below we will describe two additional species. Differences with the present species will be given in the Remarks sections of these species. + +We were unable to obtain a partial 28SrRNA sequence of this specimen. + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE1A5A2FF6788D5FA57FE84.xml b/data/38/6C/C6/386CC616DCE1A5A2FF6788D5FA57FE84.xml new file mode 100644 index 00000000000..650759a5d83 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE1A5A2FF6788D5FA57FE84.xml @@ -0,0 +1,81 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Clathrina rotundata + +Voigt +et al. +, 2017 + + + + + + +Recently described extensively in + +Voigt +et al. +2017 + +and discussed above in the Remarks of + +C. maremeccae + + +sp.nov. + + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE1A5A2FF678941FCA1FE49.xml b/data/38/6C/C6/386CC616DCE1A5A2FF678941FCA1FE49.xml new file mode 100644 index 00000000000..44c23e66a6b --- /dev/null +++ b/data/38/6C/C6/386CC616DCE1A5A2FF678941FCA1FE49.xml @@ -0,0 +1,85 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Clathrina primordialis +sensu +Row 1909 + + + + + +No +description has been given by +Row (1909: 184) +. + +Voigt +et al. +2017 + +suggested it is likely conspecific with + +Clathrina rowi + +. The original description by +Haeckel (1872) +(vol. 2: 16, as + +Ascetta + +) is from the Mediterranean. See also below in the paragraph of additional East African Calcarea). + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE1A5A2FF6789F5FA9EFDF9.xml b/data/38/6C/C6/386CC616DCE1A5A2FF6789F5FA9EFDF9.xml new file mode 100644 index 00000000000..1ed77e8e71e --- /dev/null +++ b/data/38/6C/C6/386CC616DCE1A5A2FF6789F5FA9EFDF9.xml @@ -0,0 +1,76 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucosolenia canariensis +sensu +Burton 1952 + + + + + +The specimen was greyish white and +10 cm +in diameter, but there is no further description and the identity remains uncertain. The original description by + +Miklucho-Maclay (1868: 230, as + +Nardoa + +) + +is from the Canary Islands. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE1A5A2FF678A85FCBCFC19.xml b/data/38/6C/C6/386CC616DCE1A5A2FF678A85FCBCFC19.xml new file mode 100644 index 00000000000..063cb5cf844 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE1A5A2FF678A85FCBCFC19.xml @@ -0,0 +1,89 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Clathrina tenuipilosa +sensu +Row 1909 + + + + + +Although Row’s (1909: 185) description contains many words, there are no measurements of the spicules. He describes ‘oxeas of such unusual and constant form, being very long and extremely slender’, and mentions tetractines, from which we may conclude that it is possible the identification is correct. The species has originally been described by +Dendy (1905) +from + +Sri +Lanka + +, and it has been transferred to + +Arturia + +by Klautau +et al. +(2013). +Burton (1952) +reported this species from the Egyptian part of the +Gulf +of Aqaba (as + +Leucosolenia + +), giving their size (up to +3 cm +), but failing to describe the skeleton and the spicules. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE1A5A2FF678BA5FB64FC75.xml b/data/38/6C/C6/386CC616DCE1A5A2FF678BA5FB64FC75.xml new file mode 100644 index 00000000000..e1d56d8e97f --- /dev/null +++ b/data/38/6C/C6/386CC616DCE1A5A2FF678BA5FB64FC75.xml @@ -0,0 +1,71 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Soleneiscus hamatus + +Voigt +et al. +, 2017 + + + + + + +This was recently described and for its properties the reader is referred to Voigt +et al. +’s paper. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE1A5A2FF678C11FF18FB06.xml b/data/38/6C/C6/386CC616DCE1A5A2FF678C11FF18FB06.xml new file mode 100644 index 00000000000..3d6be753efe --- /dev/null +++ b/data/38/6C/C6/386CC616DCE1A5A2FF678C11FF18FB06.xml @@ -0,0 +1,77 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucandra aspera +sensu +Row 1909 + + + + + +Row (1909: 186) +mentioned ‘a considerable number of fragments’, but failed to give taxonomic details. The original description of + +Schmidt (1862: 15, as + +Sycon asperum + +) + +is from the Adriatic. This record remains +incertae sedis +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE1A5A2FF678CC5FBCAFAA9.xml b/data/38/6C/C6/386CC616DCE1A5A2FF678CC5FBCAFAA9.xml new file mode 100644 index 00000000000..f56e532238a --- /dev/null +++ b/data/38/6C/C6/386CC616DCE1A5A2FF678CC5FBCAFAA9.xml @@ -0,0 +1,76 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucandra primigenia +sensu Row + +190 + +9 + + + +This has not been described, only listed by +Row (1909: 186) +, so it remains +incertae sedis +. + +Leucetta primigenia +Haeckel, 1872 + +is a species from the Adriatic, unlikely to occur in the Red Sea. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE1A5A2FF678D55FD40F9EC.xml b/data/38/6C/C6/386CC616DCE1A5A2FF678D55FD40F9EC.xml new file mode 100644 index 00000000000..dabcc87b9f3 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE1A5A2FF678D55FD40F9EC.xml @@ -0,0 +1,111 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucaltis bathybia +Haeckel, 1872 + + + + + +Next to Haeckel’s (1872: 156) description, there are three additional records, (1) by +Row (1909: 205) +from +Suez +as + +Leucilla bathybia + +, (2) by +Burton (1952: 164) +from the +Gulf +of Aqaba as + +Leuconia + +, and (3) by +Lévi (1965: 25) +from the + +southern +Red Sea + +, also as + +Leuconia + +. Neither Row nor Lévi provided a description, so we cannot comment. +Burton (1952) +gave a partial description, which may indicate his specimens belonged to + +Paraleucilla crosslandi + +(see above in the remarks of that species). The species as described by +Haeckel (1872: 156) +is also discussed above under + +Leucaltis nodusgordii + +and under + +Paraleucilla crosslandi +. + +Its identity remains to be decided from redescription of the +type +material, ZMB 326. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE1A5A2FF678EA9FA5AF8D4.xml b/data/38/6C/C6/386CC616DCE1A5A2FF678EA9FA5AF8D4.xml new file mode 100644 index 00000000000..e9e017a88c5 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE1A5A2FF678EA9FA5AF8D4.xml @@ -0,0 +1,92 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leuconia nausicaae +sensu +Burton 1952 + + + + + +The Mediterranean species + +Leucaltis nausicaae +Schuffner, 1877 + +was reported from the Egyptian part of the Gulf of Aqaba by +Burton (1952) +as + +Leuconia + +, but he failed to give a description. Schuffner’s species is considered a + +Leucandra + +, so we assume that Burton’s record also concerns a + +Leucandra + +. It likely does not possess giant diactines and has atrial tetractines, which makes it similar to + +Leucandra pilula + + +sp.nov. + +, but this needs further corroboration. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE1A5A5FF678F71FA98FE85.xml b/data/38/6C/C6/386CC616DCE1A5A5FF678F71FA98FE85.xml new file mode 100644 index 00000000000..ad8b2b72e48 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE1A5A5FF678F71FA98FE85.xml @@ -0,0 +1,117 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Syconella proboscidea +Haeckel, 1870 + + + + + +This combination is a clear +nomen nudum +as there is no description given in Haeckel’s 1870 paper (p. 239). In the 1872 monograph, Haeckel reassigned the name + +proboscidea + +to + +Sycandra +Haeckel, 1872 + +. Since then this genus is + + + + +restricted to a single species + +S. utriculus +( +Schmidt, 1869 +) + +(originally as + +Ute +Schmidt, 1862 + +). Most other + +Sycandra + +species are assigned to + +Sycon +Risso, 1870 + +and from the few remarks of +Haeckel (1872: 313) +it is likely that + +Sycandra proboscidea + +is also a member of that large genus. + +Sycon proboscidea +( +Haeckel, 1872 +) + +from the Egyptian Red Sea (Siemens collection) is poorly known and no recent records are available. It is a +species inquirenda +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE3A5A0FF678A62FC40F92E.xml b/data/38/6C/C6/386CC616DCE3A5A0FF678A62FC40F92E.xml new file mode 100644 index 00000000000..e428bd82f4f --- /dev/null +++ b/data/38/6C/C6/386CC616DCE3A5A0FF678A62FC40F92E.xml @@ -0,0 +1,203 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Trichogypsia + +spec. + + + + +Figs 91a–e + + + + +Material examined. +Microscopic slide ZMA.POR. + +P1616, +Seychelles +, NE of +Aride Island +, +4.2°S +55.6833°E +, depth + +40 m + +, coll. +R.W.M. van Soest +, field nr. +NIOP-E +stat. 715, + +19 December 1992 + +. Unfortunately, the specimen, from which the slide was made, has not been found again in the collections. The data provided here are meant to draw attention to the existence in the +Western Indian Ocean +of a species of this rare and peculiar genus. + + + + + +Description. +A thin red encrustation, lateral size 6 + +x +5 + +mm, thickness +2 mm +. Surface microconulose. + + +Aquiferous system +. Leuconoid. + + +Skeleton +(Figs 100a–e) In cross section (Fig. 100a) there is a cortical region consisting of a palisade of smaller diactines, forming small bouquets of 6–10 spicules (Figs 100b–c), with sharp points directed outward. The cortical palisade is carried by tangential larger diactines. The choanosome has large hollows (Fig. 100a), interpreted as wide canals, but not provided with special atrial skeleton. The main skeleton consists of vague tracts of larger diactines (Fig. 100d–e). + + +Spicules. +Asymmetrical diactines, in two distinct forms. The cortical palisade has smaller diactines (Fig. 100d), often wobbly or crooked, with the outward-directed end sharply pointed, and the inward-directed end bluntly rounded with spines and small warts, 121– +147 +–192 +x 8 +– +10.9 +–14 µm. The main skeleton consists of larger diactines (Fig. 100e), lightly spined along the entire shaft, more heavily spined at the bluntly rounded ends, 315– +426 +–530 +x 11 +– +15.4 +–18 µm. + + + + +Distribution and ecology. +Seychelles +, at +40 m +depth. + + + + +Remarks. +The genus + +Trichogypsia + +is so far confined to the North Atlantic and North Pacific. Following +Dendy & Row (1913) +, the World Porifera Database (Van + +Soest +et al. +2018 + +) recognizes three distinct species. In the North Atlantic there are Southern England’s + +T. villosa +Carter, 1871 + +and Southern Norwegian + +T. incrustans +( +Haeckel, 1872 +) + +, originally as + +Leucyssa + +. This contrasts with Burton’s (1963) opinion that the two are conspecific. Borojević +et al. +(2000) have re-examined only Carter’s (1871) slide, remarking that the internal canals are lined by special curved spicules, not noted by Carter. In the absence of a redescription of Haeckel’s material, we remain in doubt over the specific differences. Recently, +Lehnert & Stone (2017) +described a further species + +Trichogypsia alaskensis + +from the S coast of Alaska. In any case, + +T. villosa + +and + +T. incrustans + +(greyish white or greenish white) and + +T. alaskensis + +(golden brown) differ from the +Seychelles +specimen (red) in life color. Spicule lengths of the present specimen are 120–530 µm, Carter and Haeckel give 200–450 µm for the two European species, so these match closely. + +T. alaskensis + +has much larger spicules, up to 1225 +x 46 +µm. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE4A5A7FF67889DFE4BFED9.xml b/data/38/6C/C6/386CC616DCE4A5A7FF67889DFE4BFED9.xml new file mode 100644 index 00000000000..8fdcbad7b88 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE4A5A7FF67889DFE4BFED9.xml @@ -0,0 +1,76 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucandra claviformis +Schuffner, 1877 + + + + + +Schuffner (1877: 414, pl, 24 fig. 5) +described this sycon-like individual from +Mauritius +. It possesses diactines of 270–400 +x 31 +µm and only small triactines and tetractines with actines of 150–160 +x 9 +µm, whith the apical actines of the tetractines 9–40 µm long. These small spicule sizes distinguish this species from most other + +Leucandra + +species of the region. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE4A5A7FF678965FDB0FDA4.xml b/data/38/6C/C6/386CC616DCE4A5A7FF678965FDB0FDA4.xml new file mode 100644 index 00000000000..5ef721e6942 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE4A5A7FF678965FDB0FDA4.xml @@ -0,0 +1,84 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucandra falcigera +Schuffner, 1877 + + + + + +Schuffner (1877: 416, pl. 25 fig. 6) +described a tiny oval individual with short apical fringe from +Mauritius +. The spicule package is similar to that of + +L. claviformis + +, but the measurements of the actines have a distinctly larger range: the diactines are up to 900 µm, triactines have actines 54–409 +x 9–40 +µm, tetractines have basal actines 136–227 +x 13 +, with apical actines up to 40 µm long. These measurements are rather similar to those of + +L. pilula + + +sp.nov +. + +, but this species lacks the diactines. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE4A5A7FF678A61FCEFFCA1.xml b/data/38/6C/C6/386CC616DCE4A5A7FF678A61FCEFFCA1.xml new file mode 100644 index 00000000000..53486835f04 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE4A5A7FF678A61FCEFFCA1.xml @@ -0,0 +1,92 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucandra seychellensis +Hôzawa, 1940 + + + + + + +Hôzawa (1940: 158) +described an oval specimen of +3 cm +high from the +Seychelles +. It has as its most prominent feature giant oxeas of 800– +1500 x +45–65 µm arranged scattered irregularly and tangentially over the surface. +The +main skeleton is a confused arrangement of triactines of 70–260 + +x 6–30 + +µm and tetractines of similar size with apical actines + +50 x 14 + +µm. The atrial skeleton consists of sagittal triactines with larger paired actines (130–180 + +x 8–10 + +µm) and shorter unpaired actines (50– + +90 x 6–8 + +µm). + + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE4A5A7FF678B6DFF0AFB89.xml b/data/38/6C/C6/386CC616DCE4A5A7FF678B6DFF0AFB89.xml new file mode 100644 index 00000000000..408b003f7b4 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE4A5A7FF678B6DFF0AFB89.xml @@ -0,0 +1,86 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Sycortis sycilloides +Schuffner, 1877 + + + + + + +This +Mauritius +species is discussed above as a possible junior synonym of + +Sycettusa stauridia +( +Haeckel, 1872 +) + +. +It +has similar habitus (two coalescent small tubular individuals), but it has the unpaired actines of the subatrial triactines much longer and thicker (600– +1000 x +80 µm) than +Haeckel’s +and ours, which measure only 400 + +x 10–20 + +µm. + + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE4A5A7FF678C35FC75FACC.xml b/data/38/6C/C6/386CC616DCE4A5A7FF678C35FC75FACC.xml new file mode 100644 index 00000000000..7489f11f82c --- /dev/null +++ b/data/38/6C/C6/386CC616DCE4A5A7FF678C35FC75FACC.xml @@ -0,0 +1,118 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucilla proteus +Dendy, 1913 + + + + + +Dendy (1913: 26) described this species from the +Seychelles +as distinct, but very close to + +L. australiensis +( +Carter, 1886 +) + +. He suggested that it was possible that the small +Seychelles +specimens could be juveniles of the Australian species. + +L. australiensis + +was also reported from +Indonesia +(cf. Van Soest & De Voogd 2015, p. 95) and from + +South +Africa + +( +Borojević 1967, p. 221 +). +Borojević (1967) +and +Borojević & Boury-Esnault (1987b) +supported Dendy’s view and synonymized + +L. proteus + +with + +L. australiensis + +, but eventually Borojević +et al. +(2000) reassigned + +L. proteus + +to + +Paraleucilla proteus + +as a separate valid species. Above, the species is compared with + +Paraleucilla erpenbecki + + +sp.nov. + +, showing that the differences with that species are considerable. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE4A5A7FF678E3DFBEDF89C.xml b/data/38/6C/C6/386CC616DCE4A5A7FF678E3DFBEDF89C.xml new file mode 100644 index 00000000000..bc88e5bbf28 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE4A5A7FF678E3DFBEDF89C.xml @@ -0,0 +1,91 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Clathrina primordialis +sensu +Jenkin, 1908 + + + + + +Jenkin (1908: 436) +gave a short description of specimens of + +Clathrina + +with actines of 160–180 +x 16–20 +µm. He assigned these to Haeckel’s + +Clathrina primordialis + +(originally as + +Ascetta +). + +This species is reported widely in the literature but it was recently restricted to the Mediterranean ( +Klautau & Valentine, 2003 +; Klautau +et al. +2016). The spicule sizes of Jenkin’s material could indicate membership of above described + +Clathrina sinusarabica +Klautau & Valentine, 2003 + +, but the short description is insufficient for a definite conclusion. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE4A5A7FF678F39FC9FF80D.xml b/data/38/6C/C6/386CC616DCE4A5A7FF678F39FC9FF80D.xml new file mode 100644 index 00000000000..2a10dabeba9 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE4A5A7FF678F39FC9FF80D.xml @@ -0,0 +1,75 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Clathrina darwinii +sensu +Jenkin 1908 + + + + + +Jenkin (1908: 436) +decribed and illustrated specimens assigned to Haeckel’s + +Ascaltis darwinii + +from Zanzibar. This record is discussed above in the Remarks on + +Arturia sueziana + +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE5A5A6FF67889DFB5EFE49.xml b/data/38/6C/C6/386CC616DCE5A5A6FF67889DFB5EFE49.xml new file mode 100644 index 00000000000..1823adb72bf --- /dev/null +++ b/data/38/6C/C6/386CC616DCE5A5A6FF67889DFB5EFE49.xml @@ -0,0 +1,103 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Clathrina contorta +var. +spinosa +sensu +Jenkin 1908 + + + + + +Jenkin (1908: 437) +described three specimens of a pure white sponge from Zanzibar with irregularly anastomosed tubuli under this name. + +Leucosolenia contorta +( +Bowerbank, 1866 +) + +from Northeast European waters has a checkered history (cf. +Minchin 1905 +; +Klautau & Valentine 2003 +) with the current not well-established conclusion that it is a senior synonym of + +Ascetta spinosa +Von Lendenfeld, 1891 + +described from the Adriatic and now assigned to the genus + +Ascandra + +as + +Ascandra contorta + +(see Klautau +et al. +2016). How +Jenkin (1908) +came to consider his specimens to be a member of this species from Europe is not quite clear. The triactines and basal actines of the tetractines were 80–150 +x 10–12 +µm, the apical actines of the tetractines were 50– +65 x 5–7 +µm. It is likely, but not certainly a species of +Ernstia +and its pure white color may indicate it is as yet undescribed. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE5A5A6FF6789F5FBE1FDA4.xml b/data/38/6C/C6/386CC616DCE5A5A6FF6789F5FBE1FDA4.xml new file mode 100644 index 00000000000..fd13cb79e95 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE5A5A6FF6789F5FBE1FDA4.xml @@ -0,0 +1,71 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Clathrina blanca +sensu +Jenkin 1908 + + + + + +This was discussed above in the Remarks paragraph of + +Clathrina +aff. +pulcherrima + + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE5A5A6FF678A61FC54FD69.xml b/data/38/6C/C6/386CC616DCE5A5A6FF678A61FC54FD69.xml new file mode 100644 index 00000000000..94bc3960f52 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE5A5A6FF678A61FC54FD69.xml @@ -0,0 +1,82 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucosolenia irregularis +Jenkin, 1908 + + + + + +Jenkin (1908: 440, figs 88–90) +described this from Wasini Island, near Zanzibar. It has been reassigned to + +Soleneiscus + +by Borojević +et al. +(2002: 1144). + +Voigt +et al. +(2017) + +compared this with his Red Sea + +Soleneiscus hamatus + +, concluding the two are closely related but separate species. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE5A5A6FF678B15FB44FC74.xml b/data/38/6C/C6/386CC616DCE5A5A6FF678B15FB44FC74.xml new file mode 100644 index 00000000000..e9015a0b0cb --- /dev/null +++ b/data/38/6C/C6/386CC616DCE5A5A6FF678B15FB44FC74.xml @@ -0,0 +1,96 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucilla floridiana +sensu +Jenkin 1908 + + + + + +Jenkin (1908: 453) +reported the Central West Atlantic species + +Leucetta floridana +( +Haeckel, 1872 +) + +(originally as + +Leucaltis + +) from Wasini Island. He misspelled the species name (as + +floridiana + +) and transferred the species to the genus + +Leucilla + +because of the presence of ectosomal giant tetractines. + +Valderrama +et al. +(2009) + +redescribed and discussed + +L. floridana + +, restricting the occurrence of that species to the West Atlantic. They pointed out that Jenkin’s description is too limited to be able to classifiy his material and redescription is necessary. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE5A5A6FF678C11FF29FA94.xml b/data/38/6C/C6/386CC616DCE5A5A6FF678C11FF29FA94.xml new file mode 100644 index 00000000000..d82447ee4b2 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE5A5A6FF678C11FF29FA94.xml @@ -0,0 +1,87 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Sycon ampullum +sensu +Jenkin 1908 + + + + + +Jenkin (1908: 443) +described a small + +Sycon + +specimen under this name from Wasini Island. The name refers to Haeckel’s (1872: 308) + +Sycandra ampulla + +, a species from Brazil. The change of the name to + +ampullum + +is a mistake, because + +ampulla + +is a noun that is not be changed with the gender of the genus name. The data he provided are insufficient to characterize the species. Jenkin did not indicate whether it was stalked, the main feature of + +Sycon ampulla + +, so it will remain unnamed until it is redescribed (see also below under additional species from South Africa) + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE5A5A6FF678D31FA8EFA59.xml b/data/38/6C/C6/386CC616DCE5A5A6FF678D31FA8EFA59.xml new file mode 100644 index 00000000000..bef4589d3ae --- /dev/null +++ b/data/38/6C/C6/386CC616DCE5A5A6FF678D31FA8EFA59.xml @@ -0,0 +1,84 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Sycon ciliatum +sensu +Jenkin 1908 + + + + + +Jenkin (1908: 442) +reported this +North +Atlantic species, described by + +Fabricius (1780: 448, as +Spongia +) + +, from + +Zanzibar + +without data other than the size (specimens were +8 x 2 and 5 x +1.25 mm +). It is unlikely that a species from +North +Atlantic occurs in tropical East African waters. The species remains unnamed until it is redescribed. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE5A5A6FF678DE5FC45F901.xml b/data/38/6C/C6/386CC616DCE5A5A6FF678DE5FC45F901.xml new file mode 100644 index 00000000000..989842407e9 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE5A5A6FF678DE5FC45F901.xml @@ -0,0 +1,73 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Sycon munitum +Jenkin, 1908 + + + + + +Jenkin (1908: 442) +extensively described three specimens of this species from Zanzibar. + +It is characterized by having both tri- and tetractines in the tubar skeleton and the brushes of diactines at the distal cones are long and relatively thin. For details of spicules size one is referred to Jenkin’s excellent description. The species is also reported from the +South +Arabian coast by +Burton (1959) +, cf. above. + + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE5A5A6FF678ECDFE61F80C.xml b/data/38/6C/C6/386CC616DCE5A5A6FF678ECDFE61F80C.xml new file mode 100644 index 00000000000..5ed227546cb --- /dev/null +++ b/data/38/6C/C6/386CC616DCE5A5A6FF678ECDFE61F80C.xml @@ -0,0 +1,93 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucandra ananas +sensu +Jenkin 1908 + + + + + +Jenkin (1908: 444) +reported this +North +Atlantic species, originally described by + +Montagu (1814: 96, as +Spongia +) + +from + +Zanzibar + +. The sponges were small and flask-shaped. The spicules included long diactines, 700–3000 +x 28–46 +µm, triactines of the cortex and the main skeleton 180–500 +x 5–32 +µm, tetractines with basal actines 170–280 +x 6–20 +µm, apical actines +50 x 6–9 +µm. Possibly, one of the species of +Schuffner (1877) +, e.g. + +L. echinata + +could fit with Jenkin’s specimens. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE6A5A4FF678F71FC5FFF4D.xml b/data/38/6C/C6/386CC616DCE6A5A4FF678F71FC5FFF4D.xml new file mode 100644 index 00000000000..50f5e6abbfc --- /dev/null +++ b/data/38/6C/C6/386CC616DCE6A5A4FF678F71FC5FFF4D.xml @@ -0,0 +1,80 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucosolenia gardineri +Dendy, 1913 + + + + + +Dendy (1913: 2) extensively described this species from the Chagos Archipelago. It forms lobose masses of tightly anastomosed tubuli measuring 2.5 x +1.5 cm +. There are pseudopores at the surface leading to pseudatria. The + + + + +spicules include two size categories of triactines (140 +x 12 +µm and +74 x 7 +µm) and one category of tetractines with apical acties of 50 µm. The species is currently assigned to + +Ascaltis + +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE6A5A5FF678941FAF2FE56.xml b/data/38/6C/C6/386CC616DCE6A5A5FF678941FAF2FE56.xml new file mode 100644 index 00000000000..33db6f199b9 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE6A5A5FF678941FAF2FE56.xml @@ -0,0 +1,81 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Sycon coronatum +sensu +Row 1909 + + + + + +Other than the size of the specimen and its fringe, +Row (1909: 185) +has not described this material. This European species described by +Ellis & Solander 1786 +(as +Spongia +) is considered a junior synonym of + +S. ciliatum +( +Fabricius, 1780 +) + +. It is unlikely that the Red Sea specimen belongs to that species. This record remains +incertae sedis +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE6A5A5FF6789F5FA92FDC6.xml b/data/38/6C/C6/386CC616DCE6A5A5FF6789F5FA92FDC6.xml new file mode 100644 index 00000000000..e9d8cc905af --- /dev/null +++ b/data/38/6C/C6/386CC616DCE6A5A5FF6789F5FA92FDC6.xml @@ -0,0 +1,75 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Sycon raphanus +sensu +Row 1909 + + + + + +No +description has been given by +Row (1909: 185) +. The species, originally described by +Schmidt (1862) +, is Mediterranean. We assume that the +Red Sea +material belongs to a different species, remaining +incertae sedis +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE6A5A5FF678A85FC8DFC19.xml b/data/38/6C/C6/386CC616DCE6A5A5FF678A85FC8DFC19.xml new file mode 100644 index 00000000000..692e25192ef --- /dev/null +++ b/data/38/6C/C6/386CC616DCE6A5A5FF678A85FC8DFC19.xml @@ -0,0 +1,80 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Grantessa glabra +Row, 1909 + + + + + +See +Row (1909: 203, pl. 19 figs 5–6, text fig. 4) +. Discussed above in connection with possible synonymy with + +Sycettusa stauridia +( +Haeckel, 1872 +) + +. The type specimen BMNH 1912.2.1.9 was re-examined by us. It is a small tube with side oscule. It has cortical and atrial triactines much larger (400–700 µm) and diactines and pseudosagittal triactines much thicker (50–90 µm) than Haeckel’s and the above described material. For the time being it is reassigned to + +Sycettusa glabra + +, but redescription is necessary. +Burton (1952) +reported this species from the Egyptian part of the Gulf of Aqaba without a description. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE6A5A5FF678E75FA8DF8D5.xml b/data/38/6C/C6/386CC616DCE6A5A5FF678E75FA8DF8D5.xml new file mode 100644 index 00000000000..03e0bf897e6 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE6A5A5FF678E75FA8DF8D5.xml @@ -0,0 +1,92 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Ascaltis compacta +Schuffner, 1877 + + + + + +Schuffner’s description (1877: 404, pl. 25 fig. 9) points towards + +Arturia + +or +Ernstia +. It is obviously close to + +Arturia sueziana +Klautau & Valentine, 2003 + +, but these authors pointed out that Schuffner’s drawing does not show the presence of water-collecting tubes, which are so characteristic of + +A. sueziana + +. The additional argument for specific distinction, viz. the greater size of the actines of the triactines and tetractines, is not very convincing. In the absence of the type, which appears to be lost, it seems best to reassign + +A. compacta + +to + +Arturia + +as + +Arturia compacta + +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE7A5A4FF678909FBE9FE6D.xml b/data/38/6C/C6/386CC616DCE7A5A4FF678909FBE9FE6D.xml new file mode 100644 index 00000000000..61717a0cf3e --- /dev/null +++ b/data/38/6C/C6/386CC616DCE7A5A4FF678909FBE9FE6D.xml @@ -0,0 +1,110 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Dendya prolifera +Dendy, 1913 + + + + + + +Dendy +(1913: 6) described this species from the +Amirante Islands +, +Seychelles +. The species has been extensively discussed by +Borojević & Boury-Esnault (1986: 445–447) +. +It +is a soft wide tube characterized by lateral diverticules. +Spicules +comprise two categories of triactines (270 + +x 10 + +µm and 120 x 8.5 µm) and tetractines with apical actines of 99 µm. The species is currently assigned to + +Levinella + +. The collection of the Naturalis Biodiversity Center contains a slide, +ZMA + +. + +POR +.P.1170, which is assignable to the genus + +Levinella + +. Locality +Seychelles +, N of +Aride Island +, depth + +55 m + +, +Netherlands +Indian Ocean Project, + +19 December + +, 1992. + + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE7A5A4FF678A2EFAD7FD31.xml b/data/38/6C/C6/386CC616DCE7A5A4FF678A2EFAD7FD31.xml new file mode 100644 index 00000000000..e02ea756f45 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE7A5A4FF678A2EFAD7FD31.xml @@ -0,0 +1,79 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucascus simplex +sensu Dendy 1913 + + + + + +Dendy (1913: 9) reported his South Australian species (originally described by +Dendy 1892 +) from Providence Island, N of Madagascar. The type material from South Australia has been recently redescribed by + +Cavalcanti +et al. +(2013 + +: 277), including also Dendy’s (1913) record. For details one is referred to + +Cavalcanti +et al. +2013 + +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE7A5A4FF678AD6FD2EFC68.xml b/data/38/6C/C6/386CC616DCE7A5A4FF678AD6FD2EFC68.xml new file mode 100644 index 00000000000..817ffb39393 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE7A5A4FF678AD6FD2EFC68.xml @@ -0,0 +1,89 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Pericharax peziza +Dendy, 1913 + + + + + +Dendy (1913: 15) described this from +Cargados Carajos +as a species similar in spiculation to + +P. orientalis + +(as + +P. heteroraphis + +), but with a cup-shaped form, size +3.7 cm +diameter and a height of the cup of +2.9 cm +. The cup walls are +0.7 cm +in thickness and are smooth, unfurrowed. +Burton (1963) +synonymized the two, but Van Soest & De Voogd (2015) considered it a separate species, following Dendy’s decision. The inside of the cup has numerous oscular openings. The giant triactines have actines of 1400 +x 70 +µm, small choanosomal triactines have actines of 180 +x 5 +µm, cortical triactines are 100 x 5.5 µm, tetractines of the surfaces of the inner wall and canals up to 290 +x 12 +µm, apical actines slightly crooked, up to 75 µm. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE7A5A4FF678C2AFD32FA39.xml b/data/38/6C/C6/386CC616DCE7A5A4FF678C2AFD32FA39.xml new file mode 100644 index 00000000000..01126e4cc0f --- /dev/null +++ b/data/38/6C/C6/386CC616DCE7A5A4FF678C2AFD32FA39.xml @@ -0,0 +1,122 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Sycandra tabulata +Schuffner, 1877 + + + + + +Schuffner (1877: 422, pl. 25 fig. 11) +described this + +Sycon + +species from +Mauritius +, comparing it with + +Sycon elegans +(Bowerbank, 1845) + +. Its skeleton is distinct only by the thick bushes of thin fusiforms diactines (140 +x 4 +µm) in the distal cones of the radial tubes. +Borojević (1967) +in turn compared his record of + +Sycon elegans + +from + +South +Africa + +with Schuffner’s species. Since + +S. elegans + +is a Northeast Atlantic species, this may be interpreted as a suggestion that the +South +African record may indeed be better assigned to + +Sycon tabulatum +. + +Schuffner’s combination is preoccupied: it is a junior primary homonym of + +Sycandra tabulata +Haeckel, 1872 + +. +Dendy & Row (1913) +noticed this already, but assumed both homonyms belonged to + +Sycon elegans + +. In view of the fact that Bowerbank's and Haeckel's specimens were from the Mediterranean, while Schuffner's was from +Mauritius +this synonymy is judged to be unlikely. We propose here to rename Schuffner’s species as + +Sycon oscari + + +nom.nov +. + +The name is given to honor Oscar Schuffner, the author of its original name. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCE7A5A4FF678DDAFB27F878.xml b/data/38/6C/C6/386CC616DCE7A5A4FF678DDAFB27F878.xml new file mode 100644 index 00000000000..edab964b995 --- /dev/null +++ b/data/38/6C/C6/386CC616DCE7A5A4FF678DDAFB27F878.xml @@ -0,0 +1,110 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucandra echinata +Schuffner, 1877 + + + + + +Schuffner (1877: 411, pl. 24 fig. 4) +described a sycon-like individual from +Mauritius +, with diactines of 1000–2000 +x 50 +–80 µm, triactines up to 309 +x 20 +µm (smaller of about 110 µm were also present), tetractines with basal actines 110 +x 18 +µm and apical actines +40 x 9 +µm. This species haa been interpreted differently by various authors. See for a review +Burton (1963: 30 and 248) +. +Ridley (1884: 630) +reported a specimen of Schuffner’s species (as + +Leuconia + +) from D’Arros Island in the Amirantes, but failed to present a description or illustration. Dendy (1913: 23) reporting the species from +Cargados Carajos +also omitted a description, but provided a photo (his pl. 2 fig. 4) of an alleged specimen of + +L. echinata + +. A secondary homonymy has been caused by Dendy’s (1913) suggestion that Carter’s (1886) Southeast Australian + +Leuconia echinata + +could be a synonym of Schuffner’s species (indicated with a question mark), in the process reassigning Carter’s species to + +Leucandra + +. Burton (l.c.) was not in accord with this and assigned the two as different ‘named species’ to different ‘superspecies’ (our term for Burton’s misguided concept of species in the Calcarea), viz. + +Leuconia barbata + +for Carter’s species and + +Scypha ciliata + +for Schuffner’s species. Re-examination of Schuffner’s and Carter’s material is ultimately necessary to find the proper genus affiliation for Schuffner’s species. For the time being, + +Leucandra echinata + +appears the most proper combination as it is the original combination. Our material did not contain a likely member of Schuffner’s species. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCEAA5A9FF6788EAFC3AFEA6.xml b/data/38/6C/C6/386CC616DCEAA5A9FF6788EAFC3AFEA6.xml new file mode 100644 index 00000000000..20f60164d62 --- /dev/null +++ b/data/38/6C/C6/386CC616DCEAA5A9FF6788EAFC3AFEA6.xml @@ -0,0 +1,76 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leucetta primigenia +sensu +Vacelet & Vasseur 1965 + + + + + + +The species is Mediterranean. +No +description was given of the +Madagascar +material, except that it was bright yellow in color. This suggests that the record concerns + +Leucetta chagosensis + +. + + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCEAA5A9FF678965FB88FE34.xml b/data/38/6C/C6/386CC616DCEAA5A9FF678965FB88FE34.xml new file mode 100644 index 00000000000..2a03caa6552 --- /dev/null +++ b/data/38/6C/C6/386CC616DCEAA5A9FF678965FB88FE34.xml @@ -0,0 +1,66 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Lelapiella incrustans +Vacelet, 1977 + + + + + +Vacelet (1977: 358) +described this species from reef tunnels off Tuléar, Madagascar. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCEAA5A9FF678AF1FA98FC5E.xml b/data/38/6C/C6/386CC616DCEAA5A9FF678AF1FA98FC5E.xml new file mode 100644 index 00000000000..dd0af8da968 --- /dev/null +++ b/data/38/6C/C6/386CC616DCEAA5A9FF678AF1FA98FC5E.xml @@ -0,0 +1,95 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Clathrina cerebrum +sensu +Borojević, 1967 + + + + + +Borojević (1967: 192) +reported this Mediterranean species, originally described by + +Haeckel (1872: 54, as + +Ascaltis + +) + +, from Kwazulu Natal, Eastern South Africa. The Mediterranean species has been reassigned to + +Borojevia + +by Klautau +et al. +2016. Like the Mediterranean + +B. cerebrum + +, Borojević’s specimen has tripods of 60–100 +x 20–32 +µm, unlike the three + +Borojevia + +species described above. Like these three species the South African specimen has spined apical actines of the tetractines. This record likely represents an additional undescribed species of + +Borojevia + +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCEAA5A9FF678BFDFC5AFA95.xml b/data/38/6C/C6/386CC616DCEAA5A9FF678BFDFC5AFA95.xml new file mode 100644 index 00000000000..3953aafe909 --- /dev/null +++ b/data/38/6C/C6/386CC616DCEAA5A9FF678BFDFC5AFA95.xml @@ -0,0 +1,106 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Sycon ampulla +sensu +Borojević, 1967 + + + + + +Borojević (1967: 194) +reported the occurrence of this +South +American species, described by + +Haeckel (1872: 308, as + +Sycandra + +) + +, from the southern and eastern coast of + +South +Africa + +. Like Haeckel’s species this is a stalked + +Sycon + +. Borojević’s claim that the +South +African specimens are very similar to the +South +American specimens cannot be corroborated, as there are clear differences: Haeckel states that the stalk consists mostly of long diactines of up to +1.5 mm +long, whereas these of + +South +Africa + +are only up to 200 µm. The characteristically swollen unpaired actines of the atrial and peduncular tri- and tetractines are not mentioned or pictured by Haeckel. We believe the +South +African material does not belong to + +Sycon ampulla +( +Haeckel, 1872 +) + +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCEAA5A9FF678D31FBB2F991.xml b/data/38/6C/C6/386CC616DCEAA5A9FF678D31FBB2F991.xml new file mode 100644 index 00000000000..b8e0edf7206 --- /dev/null +++ b/data/38/6C/C6/386CC616DCEAA5A9FF678D31FBB2F991.xml @@ -0,0 +1,105 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Sycon elegans +sensu +Borojević 1967 + + + + + +Borojević (1967: 201) +reported this +North +Atlantic species (cf. +Bowerbank, 1864 +) from the Durban coast, admitting that this was the southernmost occurrence of the species. Simultaneously he referred Burton’s (1933) record of +West +Pacific + +Sycon gelatinosum +( +Blainville, 1834 +) + +and East African + +Sycon tabulatum +( +Schuffner, 1877 +) + +to the very similar + +S. elegans + +. As we pointed out above, + +Sycon tabulatum + +appears the more likely identity for this record, as + +S. elegans + +and + +S. gelatinosum + +have their +type +localities at a great distance from East Africa. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCEAA5A9FF678E3DFBE5F979.xml b/data/38/6C/C6/386CC616DCEAA5A9FF678E3DFBE5F979.xml new file mode 100644 index 00000000000..a5f20152fbc --- /dev/null +++ b/data/38/6C/C6/386CC616DCEAA5A9FF678E3DFBE5F979.xml @@ -0,0 +1,66 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Sycon natalense +Borojević, 1967 + + + + + +Borojević (1967: 200) +described this very characteristic species from the Natal coast. It has a peculiar arrangement of the diactines at the distal cones, not in a brush as is usual, but arranged along the distal part of the radiating tubes. Additionally, the subatral tri- and tetractines have the paired actines strongly different in length, which is very characteristic. For further detail see Borojević’s description and illustrations. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCEAA5A9FF678F05FE2FF820.xml b/data/38/6C/C6/386CC616DCEAA5A9FF678F05FE2FF820.xml new file mode 100644 index 00000000000..586aad2cb72 --- /dev/null +++ b/data/38/6C/C6/386CC616DCEAA5A9FF678F05FE2FF820.xml @@ -0,0 +1,81 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leuconia armata +Urban, 1908 + + + + + +This was described by +Urban (1908: 24) +and found again by +Brøndsted (1931: 38) +and +Borojević (1967) +along the eastern and southern coasts of South Africa. The species is a + +Leucandra + +with as most characteristic feature microdiactines surrounding single large diactines protruding from the surface. For more details of + +Leucandra armata + +see +Borojević (1967) +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCEBA5A8FF67889DFD9FFE34.xml b/data/38/6C/C6/386CC616DCEBA5A8FF67889DFD9FFE34.xml new file mode 100644 index 00000000000..87e9ee0db4b --- /dev/null +++ b/data/38/6C/C6/386CC616DCEBA5A8FF67889DFD9FFE34.xml @@ -0,0 +1,82 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Leuconia glomerosa +Bowerbank, 1873 + + + + + +Bowerbank (1873: 17) +described a mass of coalesced tubes from Port Elizabeth. Subsequently, this same species was found in +Western +India +, described by +Dendy (1916) +and in +West +Australia +( +Row & Hôzawa 1931, not described +). The skeleton is inarticulate and the spicules include a sheath of cortical giant diactines underneath a thin layer of small triactines, and supported by subcortical pseudosagittal triactines. The tubar skeleton is formed by the longest actine of the subcortical triactines and the unpaired actines of atrial triactines. The atrial skeleton consists mostly of triactines, but there are also relatively rare tetractines. The species has been reassigned to + +Heteropia glomerosa + +by +Dendy (1916) +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCEBA5A8FF6789D1FDD9FD31.xml b/data/38/6C/C6/386CC616DCEBA5A8FF6789D1FDD9FD31.xml new file mode 100644 index 00000000000..6279fd8ecec --- /dev/null +++ b/data/38/6C/C6/386CC616DCEBA5A8FF6789D1FDD9FD31.xml @@ -0,0 +1,81 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Grantessa ramosa +sensu +Borojević 1967 + + + + + +Borojević (1967: 204) +assigned specimens from Natal (along with specimens from more westward coasts of + +South +Africa + +) to Haeckel’s (1872) + +Sycandra ramosa + +. This was originally described likewise from + +South +Africa + +, including Natal. Haeckel’s description and drawings (p. 358, pl. 54 fig.1, 58 fig. 8) and those of Borojević do not resemble each other very well. Borojević’s assumption that Haeckel failed to recognize or draw pseudosagittal subcortical triactines remains uncorroborated. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCF1A5B4FF678E15FB8CFACC.xml b/data/38/6C/C6/386CC616DCF1A5B4FF678E15FB8CFACC.xml new file mode 100644 index 00000000000..5f19a5cf45b --- /dev/null +++ b/data/38/6C/C6/386CC616DCF1A5B4FF678E15FB8CFACC.xml @@ -0,0 +1,352 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Paraleucilla crosslandi +( +Row, 1909 +) + + + + + +Figs 82a–h + + + + + + +Leucilla crosslandi + +Row, 1909 +: 207 + + +, fig. 6. + + + + + +Leucandra innominata + +Dendy & Row, 1913 +: 774 + + +. + + + + +Paraleucilla crosslandi + +; Borojević +et al. +2002: 1180. + + + + + + +Material +examined. + +ZMA +Por. 13439. +Israel +, +Gulf of Aqaba +, +Red Sea +, depth + +7 m + +, scuba, coll. +M. Wunsch +, field nr. AQ + +7, 30 June + +1998. + + + + + +Description. +Fragment of a short, squat, tube ( +Fig. 82a +), white in life and in alcohol. Size +9 mm +high, +6 mm +in diameter, terminal oscule +3 mm +. Consistency firm. + + +Aquiferous system +. Leuconoid. + + + +FIGURE 82. + +Paraleucilla crosslandi +(Row, 1909) + +, ZMA Por. 13439, from Gulf of Aqaba, a, habitus (scale bar = 1 cm), b, light microscopic images of cross section of skeleton, c–g, SEM images of the spicules, c, cortical triactine, d, (sub)cortical tetractines, e, large choanosomal triactines, f, large subatrial tetractines, g, atrial triactines. + + + +Skeleton. +( +Fig 82b +) In cross section of the wall there is a cortical skeleton of triactines and the unpaired and paired actines of cortical tetractines. The subcortical skeleton is inarticulate consisting of the apical actines of the cortical tetractines and the unpaired actines of ‘subatrial’ tetractines, which have a position in the middle of the wall. The mid-skeletal and subatrial region contains a confused mass of smaller tetractines, carried by a layer of smaller triactines lining the atrial cavity. + + +Spicules. +( +Figs 82c–h +) Cortical triactines, giant tetractines, choanosomal triactines, subatrial tetractines, atrial triactines. + + +Large triactines, cortical ( +Fig. 82c +) and mid-skeleton ( +Fig. 89e +), which are indistinguishable morphologically; regular or slightly sagittal, actines 198–273–336 +x 10 +– +17.9 +–27 µm. + + +Giant tetractines ( +Fig. 82d +), cortical, and mid-skeleton tetractines (these are not easily distinguishable morphologically), sagittal to irregular, often with arched paired actines and opposing unpaired and apical actines; unpaired actines 204– +481 +–720 +x 23 +– +76.7 +–98 µm, paired actines 540– +722 +–920 +x 21 +– +56.3 +–88 µm, apical actines 233– +718 +–1030 +x 39 +– +70.1 +–78 µm. + + +Small tetractines of the subatrial skeleton ( +Fig. 82f +), sagittal, upaired actines 80– +155 +–211 +x 8 +– +10.2 +–11 µm, paired actines 120–191–282 +x 8 +– +10.4 +–11 µm, apical actines 24– +35 +– +48 x 7 +– +8.2 +–9 µm. + + +Small triactines of the atrial skeleton ( + +Fig. +82g + +), 63– +118 +–200 +x 8 +– +10.3 +–14 µm. + + + + +Distribution and ecology. +Red Sea +, shallow depth. + + + + +Remarks. +The present specimen conforms closely with Row’s description. However, descriptions by +Haeckel (1872, p. 156–157) +, of + +Leucaltis bathybia +var. +perimina + +(from a depth of +615 m +) and + +L. b. +var. +arabica + +(shallow depth) from the +Red Sea +remind of the present species. Various authors assigned these names to different genera: + +Leucaltis + +, + +Leuconia + +, + +Leucilla + +and + +Sycettusa + +. There are insufficient details in Haeckel’s decriptions to decide whether + +Leucaltis bathybia + +is a senior synonym of + +Paraleucilla crosslandi + +. +Burton (1952) +reported + +L. bathybia + +(as + +Leuconia + +) from the +Gulf +of Aqaba giving measurements of the giant tetractines only, ranginging from 400–960 +x 32 +–90 µm. Given these large sizes it is possible that Burton’s specimens conform to + +P. crosslandi + +, but in the absence of further spicule measurements this cannot be ascertained. Remarkably, Burton did not discuss Row’s species. Unfortunately, also +Lévi (1965) +when reporting this species (as + +Leuconia bathybia + +) failed to give a description. + + +Dendy & Row’s (1913) new name + +Leucandra innominata + +, erected to remove the junior secondary homonymy of Row’s + +Leucilla crosslandi + +with Thacker’s (1908) + +Leucandra crosslandi + +, is no longer necessary because the homonymy of the two species names involved has been removed as they are reassigned to different genera. Because the replacement name + +Leucandra innominata + +was only used once in Burton’s (1963: 546) listing under the alleged senior synonym + +Amphoriscus saccharata + +(along with + +Leucilla crosslandi + +), which does not count as ‘use’ in the sense of ICZN art. 59.3, the name + +Paraleucilla crosslandi +( +Row, 1909 +) + +is reinstated. + +Unfortunately, we were unable to obtain a partial 28S sequence for this species. + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCF3A5B2FF678C5CFC6DFA1C.xml b/data/38/6C/C6/386CC616DCF3A5B2FF678C5CFC6DFA1C.xml new file mode 100644 index 00000000000..488f0647dcd --- /dev/null +++ b/data/38/6C/C6/386CC616DCF3A5B2FF678C5CFC6DFA1C.xml @@ -0,0 +1,285 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Amphoriscus semoni +Breitfuss, 1896 + + + + + +Figs 80a–e +, +81a–d + + + + + +Amphorisus + +semoni + +Breitfuss, 1896 +: 435 + + +; Breitfuss 1898: 221; Van Soest & De Voogd 2015: 93, figs 68a–f. + + + + + + + +Material +examined. + +ZMA +Por. 10527, +Seychelles +, NE of +Aride Island +, +4.1667°S +55.7333°E +, depth + +55 m + +, +Agassiz +trawl, coll. +R.W.M. van Soest +, field nr + +. NIOP-E stat. 714/ +01, 19 December +1992. + + + + +Description. +The sample consists of a dozen small thin tubes ( +Fig. 80a +), which are mostly loose, but two tubes are attached together to a small stone. It is likely the tubes were in contact on the substratum. Live color reported as white, in alcohol they become beige. Size of individual tubes +1–3 cm +high, +5–9 mm +in diameter. Apical oscules naked. Consistency soft. + + +Aquiferous system +. Syconoid. + + +Skeleton. +( +Figs 80b–e +) Inarticulate ( +Fig. 80b +). The cortical skeleton ( +Figs 80c–d +) is formed by the unpaired and paired actines of giant tetractines. The apical actines of the ectosomal tetractines form the choanosomal skeleton together with the unpaired actines of subatrial sagittal triactines. The subatrial skeleton is formed by the paired actines of sagittal triactines and all actines of smaller triactines. The atrial skeleton ( +Fig. 80e +) is formed by small tetractines, the apical actines of which protrude into the atrial lumen. + + +Spicules. +( +Figs 81a–d +) Giant tetractines, triactines, small tetractines. + + +Giant tetractines ( +Fig. 81a +), with straight or curved actines of rather variable length and thickness, unpaired actines 162– +264 +–487 +x 12 +– +20.1 +–31 µm, paired actines 210– +336 +–552 +x 12 +– +21.1 +–29 µm, apical actines 239– +425 +–882 +x 13 +– +21.8 +–31 µm. + + +Triactines ( +Figs 81b–c +), divisible in overlapping larger and smaller spicules: + + +Large triactines ( +Fig. 81b +), sagittal, usually with unpaired actines slighty shorter; unpaired actines 200– +266 +–342 +x 13 +– +14.8 +–18 µm, paired actines 279– +309 +–336 ≈ 12– +13.3 +–15 µm. + + +Small triactines ( +Fig. 81c +), slightly sagittal, unpaired actines 48– +137 +–180 +x 7 +– +9.4 +–14 µm, paired actines 88– +178 +–246 +x 6 +– +8.8 +–11 µm. + + + +FIGURE 80. + +Amphoriscus semoni +Breitfuss, 1896 + +, ZMA Por. 10527 from the Seychelles, a, habitus of group of individuals (scale bar = 1 cm), b–e, SEM images of skeleton, b, cros section of body wall, c, overview from above of peripheral skeleton, d, detail of peripheral skeleton, e, overview from above of atrial skeleton. + + + +Small tetractines ( +Figs 81d +), sagittal, often with curved or wobbly paired actines; unpaired actines 81– +150 +–241 +x 7 +– +9.4 +–11 µm, paired actines 121– +214 +–269 +x 7 +– +9.8 +–12 µm, apical actines 15– +54 +– +94 x 3 +– +5.2 +–7 µm. + + + + +Distribution and ecology. +Indonesia +, +Seychelles +, shallow-water down to + +55 m +. + + + + + +Remarks. +We assign this material to the Indonesian species + +A. semoni + +because of overall similarity with recently described material (cf. Van Soest & De Voogd 2015). However, there are several discrepancies: the tubes of the Indonesian ZMA Por. 0 8073 were described as green in life, and they also appeared slightly different in shape as their diameter gradually narrowed down towards the substratum, whereas our present specimens were white in life and and remain cylindrical over most of their length. The apical actines of the giant tetractines of the Indonesian specimens penetrated through the atrial wall, which we do not observe in the present specimens. We consider these differences as +minor +and subject to variation. + + + +FIGURE 81 +. + +Amphoriscus semoni +Breitfuss, 1896 + +, ZMA Por. 10527, SEM images of the spicules, a, giant tetractines, b, giant triactine, c, subatrial triactine, d, atrial tetractines. + + + +The South African + +Amphoriscus kryptoraphis +Urban, 1908 + +, from deeper water ( +155 m +) differs from the above a.o. by the possession of trichoxeas. Unfortunately, our attempt to obtain partial 28S sequences failed. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCF7A5B8FF678DA2FC46FE56.xml b/data/38/6C/C6/386CC616DCF7A5B8FF678DA2FC46FE56.xml new file mode 100644 index 00000000000..b680f4d68cd --- /dev/null +++ b/data/38/6C/C6/386CC616DCF7A5B8FF678DA2FC46FE56.xml @@ -0,0 +1,527 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Paraleucilla erpenbecki + +sp.nov. + + + + +Figs 83a–d +, +84a–i + + + + +Material examined. +Holotype +, +ZMA +Por. 22409a, +Mozambique +Channel, between +Mozambique +and +Madagascar +, E of Juan de Nova +Island +, +17.2817°S +43.1567°E +, depth +60 m +, coll. RV ‘Pelagia’ Around Africa II expedition, leg 6, field nr. 20- +ASC +10, 1 April +2001 + + +Paratypes +, +ZMA +Por. 22409c, five individuals from the same locality as the +holotype +. + + + + +Description. +The sample consists of six sycon-like tubular individuals ( +Figs 83a,a +1 +), one of which was chosen as the +holotype +( +Fig. 83a +). Shape oval, narrowing towards the osculum. Height of largest tube (the +holotype +) is +3 cm +, diameter +1.5 cm +. Fringe prominent but short, +2–3 mm +, slightly flaring. Color in alcohol light beige. Surface slightly hispid, rough-looking. Consistency soft. + + +Aquiferous system +. Leuconoid. + + +Skeleton. +( +Figs 83b–d +) The wall has a thickness of about +2 mm +with protruding trichoxeas and very few diactines causing the hispid surface. In the SEM cross section ( +Fig. 83b +), from the periphery towards the atrium, there is a cortical skeleton ( +Fig. 83c +) of rare triactines carried by the basal actines of a single layer of cortical tetractines. Occasionally, there are scattered diactines protruding from the skeleton to the outside. Next, the choanosomal skeleton is inarticulate ( +Fig. 83b +) formed by the apical actines of the cortical tetractines and unpaired actines of giant triactines lying in the mid-region of the wall. Below these there is a confused mass of smaller tetractines and triactines, and finally the atrial skeleton ( +Fig. 83d +) is formed by tetractines of which the apical actines protrude far into the atrial lumen, and by smaller triactines. The fringe is formed by thin giant diactines grading into thick trichoxeas, and at the base it is supported by triactines and tetractines (not shown). + + +Spicules. +( +Figs 84a–i +) Giant diactines, trichoxeas, small diactines, large tetractines, large triactines, small tetractines and small triactines. + + +Giant diactines (Fg. 84a), fusiform, blunt endings, 388– +1066 +– +1973 x 19 +– +31.8 +–42 µm. + + +Trichoxeas and thin diactines ( +Fig. 84b +), sharp endings but subapically often slightly distended, almost invariably broken, fragements measuring 480– +962 +– +1740 x 3 +– +4.8 +–7 µm. + + +Small diactines ( +Fig. 84c +), not common, only a few could be measured, 147–210 +x 8–9 +µm. + + +Cortical triactines and small triactines of the subatrial region ( +Figs 84d +), these were indistinguishable and not very common, either regular or slightly irregular or sagittal, actines 138– +196 +–266 +x 8 +– +10.9 +–16 µm. + + +Cortical large tetractines ( +Fig. 84e +), not very common, with basal actines often curved and blunt ending, apical actines straight and pointed, thinner than the other actines; unpaired actines 132– +324 +–468 +x 13 +– +30.5 +–37 µm, paired actines 216– +304 +–429 +x 15 +– +21.7 +–31 µm, apical actines 211– +321 +–786 +x 18 +– +17.1 +–23 µm. + + +Giant triactines ( +Figs 84f +), sagittal with straight unpaired actines and curved paired actines; unpaired actines 151– +320 +–603 +x 10 +– +20.4 +–33 µm, paired actines 231– +366 +–598 +x 12 +– +22.2 +–36 µm. + + +Giant tetractines of the subatrial region ( + +Fig. +84g + +), with straight actines, apical actines short and conical; unpaired actines 231– +394 +–696 +x 13 +– +18.8 +–38 µm, paired actines 228– +313 +–391 +x 12 +– +16.7 +–26 µm, apical actines 45– +62 +– +84 x 7 +– +8.3 +–10 µm. + + +Small tetractines of the subatrial region ( +Fig. 84h +), similar in shape to giant tetractines, but smaller, unpaired actines 48– +149 +–268 +x 7 +– +10.4 +–13 µm, paired actines 63– +151 +–249 +x 6 +– +9.0 +–11 µm, apical actines 31– +47 +– +61 x 5 +– +7.2 +–10 µm. + + +Atrial tetractines ( + +Fig. +84i + +), with long straight apical actines and unpaired actines almost similar in length, with curved paired actrines; unpaired actines 152– +232 +–418 +x 9 +– +11.3 +–13 µm, paired actines 174– +285 +–461 +x 8 +– +9.1 +–12 µm, apical actines 66– +167 +–234 +x 8 +– +8.9 +–10 µm. + + + + +Distribution and ecology. +Mozambique +Channel, at +60 m +depth. + + + + +Etymology. +Named after Dr. Dirk Erpenbeck, München, +Germany +, in recognition of his great efforts to integrate molecules and morphology in the classification of the Porifera. + + + + +Remarks. +The new species is assigned to + +Paraleucilla + +on account of the skeletal zonation of an inarticulate subcortical skeleton formed by the apical actines of the cortical tetractines and the unpaired actines of giant triactines in the mid region of the choanosome, followed by a confused choanosomal and subatrial skeleton. + + +A regional species is + +Paraleucilla proteus +(Dendy, 1913) + +(originally as + +Leucilla + +). It has the same shape (although much smaller: only +7 mm +high) as our new species. Differences are that almost all spicules, excepting the subcortical tetractines, are considerably smaller in size, notably the giant triactines do not seem to be represented, the apical actines of the atrial tetractines are much shorter, and there are no giant diactines (though smaller diactines are present). There are also no cortical small triactines. Dendy suggested that his small specimens were juveniles of the Australian species + +Leucilla australiensis +( +Carter, 1886 +) + +, but eventually Borojević +et al. +(2000) assigned Dendy’s species to + +Paraleucilla + +. + + +A further geographically close species is + +Paraleucilla cucumis +( +Haeckel, 1872 +) + +(p. 205, as + +Leucandra + +) from +Sri Lanka +and + +South +Australia + +, differing a.o. in the presence of subcortical +and +mid-region tetractines (the latter not present in our new species), and the absence of mid-region and atrial triactines, with as a consequence the absence of apical actines protruding into the atrial lumen. There is a small nomenclatorial problem, because +Hackel (1872) +divided his + +Leucandra cucumis + +into two (?) varieties (‘spezifische Varietäten’), + +L.c. +var. +bassensis + +and + +L.c. +var. +palcensis + +. The difference was the virtual absence ( +bassensis +) and presence ( +palcensis +) of giant diactines. The difference was apparently considered trivial because neither +Dendy (1892) +and +Dendy & Row (1913) +, nor + +Cavalcanti +et al. +(2014) + +make mention of these varieties. We formally need to indicate which one of the varieties is the nominotypical variety (ICZN art. 47). In view of the redescription by +Dendy (1892) +it makes sense to consider the + +var. +bassensis + +as the typical variety, to be named + +Leucandra cucumis +var. +cucumis + +, with the + +var. +palcensis + +as a junior synonym. The latter name would then be available if future research would result in distinction of an Indian Ocean species differing from the Bass Strait + +Paraleucilla cucumis + +. + + + +FIGURE 83. + +Paraleucilla erpenbecki + + +sp.nov +. + +, a, habitus holotype ZMA Por. 22409a, from the Mozambique Channel, a1 habitus of paratypes ZMA POR. 22409c, from the same location (scale bar = 1 cm), b–d, SEM images of skeleton, b, cross section, c, overview from above of peripheral skeleton, d, overview from above of atrial skeleton. + + + +The new species is close to West Australian + +Paraleucilla princeps +( +Row & Hôzawa, 1931 +) + +(as + +Leucilla princeps + +, p. 799, pl. 21 fig. 17, text-fig. 16), sharing tubular shape and most of the spicule complement. Also the sizes of the spicules conform rather closely. A major difference is the absence of giant triactines in the choanosomal skeleton. These spicules are a dominant feature of the present species, forming the skeletal structure of the peripheral inarticulate skeleton together with the apical actines of the subcortical tetractines. Row & Hôzawa do mention the presence of similar shaped smaller triactines but these only occur in the oscular region. Also not present are the small diactines. + + + + +FIGURE 84 +. + +Paraleucilla erpenbecki + + +sp.nov +. + +, ZMA Por. 22409a, SEM images of the spicules, a, giant diactine, b, trichoxea fragament, c, rare microdiactine, d, cortical and atrial triactines, e, (sub)cortical tetractine, f, giant choanosomal triactines, g, giant choanosomal tetractine, h, subatrial tetractine, I, atrial tetractine. + + + + + +Paraleucilla dalmatica + +Klautau +et al. +2017 + + +from the Mediterranean is similar in shape and skeletal structure, but spicule sizes differ significantly. Also, Brazilian + +P. incomposita + +Cavalcanti +et al. +2014 + + +is close in shape and structure but differs also in spicule sizes. Recently ( +Chagas & Cavalcanti 2017 +), it was discovered that this species possesses choanosomal pentactines as a remarkable unique feature. + + +We obtained a 28S partial gene sequence for the +holotype +and compared it with a sequence downloaded from GenBank of Mediterranean + +Paraleucilla + +spec. (supposedly the same as + +P. magna + +Klautau +et al. +, 2004 + + +), which grouped together in our Phylogeny of +Fig. 3 +at a moderate bootstrap frequency (77%). From a separate investigation of a trimmed alignment of 295 sites obtained for the two sequences we found that + +P. erpenbecki + + +sp.nov. + +differs in 8 sites from the Mediterranean + +Paraleucilla + +spec. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCFBA5B8FF678A60FAF3FBAB.xml b/data/38/6C/C6/386CC616DCFBA5B8FF678A60FAF3FBAB.xml new file mode 100644 index 00000000000..0484c41919e --- /dev/null +++ b/data/38/6C/C6/386CC616DCFBA5B8FF678A60FAF3FBAB.xml @@ -0,0 +1,118 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + +Genus + +Kebira +Row, 1909 + + + + + + + +Remark. +Up until now, the genus + +Kebira + +is monotypical and restricted to the +Red Sea +( +Row 1909 +; +Burton 1952 +; +Ilan & Vacelet 1993 +; Borojević +et al. +2000, 2002b). The skeleton of the so far only species, + +K. uteoides +Row, 1909 + +is characterized by the possession of tracts of peculiar ‘nail-shaped’ triactines, in addition to giant diactines and two forms of sagittal triactines. We also encountered specimens of this species at Jeddah in the Saudi Arabian part of the +Red Sea +(see below). However, sponges with the spicule complement mentioned above, including the ‘nailshaped’ triactines, are here reported from outside the +Red Sea +, viz. +Eastern + +South +Africa + +and the +Seychelles +. The similarity of these specimens with +Red Sea + +Kebira uteoides + +is considerable, but the atrial spicules (exclusively sagittal triactines with short unpaired actine in the +Red Sea + +Kebira + +’s) include also similarly shaped sagittal tetractines with short conical apical actines. We propose to distinguish the +South +African tetractine-bearing specimens as a separate species of + +Kebira + +, described below. The specific status of the small tetractine-bearing specimen from the +Seychelles +is kept undecided because of considerable differences with the new species. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCFBA5BDFF678C71FEA4FF4C.xml b/data/38/6C/C6/386CC616DCFBA5BDFF678C71FEA4FF4C.xml new file mode 100644 index 00000000000..6bb40de87ab --- /dev/null +++ b/data/38/6C/C6/386CC616DCFBA5BDFF678C71FEA4FF4C.xml @@ -0,0 +1,380 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Kebira uteoides +Row, 1909 + + + + + +Figs 85a–g +, +86a–e + + + + + + +Kebira uteoides + +Row, 1909 +: 210 + + +, pl. 20 figs 8–9, text-figs 7–8; + +Burton 1952 +: 164 + +; + +Ilan & Vacelet 1993 +: 110 + +, figs 2–4. + + + + + + + +Material +examined. + +RMNH +Por. 9563, +Saudi Arabia +, +Jeddah +, near +Thuwal +, +Al Fahal N +, +22.300194°N +38.959583°E +, depth + +12 m + +, coll. +N.J. de Voogd +, scuba, field nr. THU04/JED052, + +8 November 2014 + + +; + +RMNH +Por. 9664, +Saudi Arabia +, +Jeddah +, near +Thuwal +, +Um Albalam +, +22.193556°N +38.9475°E +, depth + +15 m + +, scuba, coll. +N.J. de Voogd +, field nr. THU10/JED168, + +12 November 2014 + + +. + + + + +Description. +Squat, laterally flattened, irregularly tubular individuals ( +Figs 85a–d +), attached to vertical walls and hanging down from the ceiling of cavities, with large apical or lateral oscules. In life ( +Figs 85a,c +), colors are shades of grey and pinkish white, on deck ( +Figs 85b,d +) and in preservation they become yellow. Size up to +4 cm +high, and 5 + +x +3 + +cm in lateral expansion. Oscules +4–6 mm +in diameter. Surface smooth. Consistency firm to hard. + + +Aquiferous system +. Leuconoid. + + +Skeleton. +( +Figs 85e–g +) In cross section ( +Fig. 85e +), there is a cortical skeleton of sagittal triactines, mostly with long unpaired actines ( +Fig. 85f +), carried by tangentially arranged giant diactines. Underneath, the choanosomal skeleton is formed by perpendicular giant diactines, tracts of nail-shaped triactines (arrows in +Fig. 85e +) and large sagittal triactines with long unpaired actines. The atrial skeleton ( + +Fig. +85g + +) is predominantly formed by sagittal triactines with short unpaired actines. + + +Spicules. +( +Figs 86a–e +) Giant diactines, nail-shaped triactines, sagittal triactines, microdiactines. + + +Giant and smaller diactines ( +Fig. 86a +), fusiform, symmetrical, sharply pointed, in a wide size range, 540– + +1489 +–2022 + + +x 25– +79 + +–108 µm. + + +Nail-shaped triactines ( +Figs 86b,b +1 +), thinly fusiform, pointed at one end, at the opposite end provided with two conical actines arranged at a slight angle, in a large size range, unpaired actines 105– +317 +–477 x 5.5– +8.5 +–10 µm, paired actines 3–7 +x 3 +µm. + + + +FIGURE 85. + +Kebira uteoides +Row, 1909 + +, a, habitus in situ of RMNH Por. 9664, from Jeddah (Saudi Arabia), b, the same on deck, c, habitus in situ of RMNH Por. 9563, from Jeddah (Saudi Arabia), d, the same on deck (photos N.J. de Voogd), e–g, SEM images of skeleton of RMNH Por. 9664, e, cross section, f, overview from above of peripheral skeleton, g, overview from above of atrial skeleton. + + + +Large sagittal triactines ( +Fig. 86c +), with long unpaired actines, and flaring paired actines; unpaired actines 306– +371 +–462 +x 7 +– +7.9 +–8.5 µm, paired actines 204– +227 +–248 +x 9 +– +10.4 +–12 µm. + + +Atrial sagittal triactines ( +Figs 86d +) with short unpaired actines and straight paired actines; unpaired actines 57– +86 +–121 x 8.5– +10.1 +–12 µm, paired actines 179– +228 +–282 x 11.5– +13.9 +–17 µm. + + + +FIGURE 86. + +Kebira uteoides +Row, 1909 + +, RMNH Por. 9664, SEM images of the spicules, a, giant diactine, b, nail-shaped triactines, b1, detail of nail-shaped triactine, c, triactine with long unpaired actine, d, triactines with short unpaired actines, e, microdiactine (not previously reported, so perhaps not proper), e1, details of both ends of microdiactine. + + + +Small thin diactines with tiny spines at both ends ( +Figs 86e,e +1 +), rare, not certainly proper to the sponge, but sufficiently characteristic to be a possible, previously unobserved, spicule type, 51–102 +x 2–7 +µm. + + + + +Distribution and ecology. + +Northern +Red Sea + +: +Gulf +of +Suez +, +Egypt +(Sharm-al-Sheik), +Saudi Arabia +(Jeddah), hanging down in caves on shallow water reefs. + + + + +Remarks. +The only noteworthy difference with Row’s description of the +type +specimen is that he confused the position of the cortical and the atrial sagittal triactines. It can be clearly seen in our + +Fig. +85g + +, showing the atrial surface, that the predominant spicule +type +is the sagittal triactine with short unpaired actine. In +Figs 85e +(upper part) and f, the dominant spicule +type +is the long-shafted sagittal triactine clearly visible. Our spicule sizes are more or less the same as in Row’s specimen, although we did not observe giant diactines of +4 mm +length. + +The small spined diactines may or may not be proper to the sponge. + +Burton (1952) +did not give a description other than mentioning that his specimen from Sharm al Sheik ( +Egypt +) was +2 cm +high. + + +Ilan & Vacelet (1993) +found giant diactines up to +4 mm +, but omitted further spicule measurements, concentrating on a description of the soft parts. + + +We obtained partial 28SrRNA sequences for the two specimens. In our Phylogeny of +Fig. 3 +, these grouped along with the new + +Kebira + +species described below in a larger clade together with + +Ute ampullacea + +, + +Paragrantia waguensis +Hôzawa, 1940 + +, and + +Grantiopsis heroni +Wörheide & Hooper, 2003 + +. These species were added to our analysis to confirm the affiliation of + +Kebira + +. The position of + +Ute ampullacea + +(cf. also above) in the group is surprising, but + +Kebira +, +Grantiopsis + +and also + +Paragrantia + +(see Van Soest +et al. +2015) are likely members of the gamily +Lelapiidae +. + + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCFDA5A0FF678C4AFBDBFED9.xml b/data/38/6C/C6/386CC616DCFDA5A0FF678C4AFBDBFED9.xml new file mode 100644 index 00000000000..343fdd0d0d6 --- /dev/null +++ b/data/38/6C/C6/386CC616DCFDA5A0FF678C4AFBDBFED9.xml @@ -0,0 +1,240 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Kebira + +spec. + + + + +Figs 90a–g + + + + +Material examined. +ZMA +Por. 10379b, +Seychelles +, +Mahé +, E coast, N of Moyenne Island, +4.6167°S +55.5167°E +, depth +1–7 m +, reef, snorkeling, coll. R.W.M. van Soest, field nr. +NIOP-E +stat. 606, +10 December 1992 +. + + + + +Description. +The specimen is small and tubular ( +Fig. 90a +), about +1.5 cm +high, +0.5 cm +in diameter, with a narrow apical oscule. Color in alcohol dirty white. Surface smooth and shining, due to a thick surface armor of tangential giant diactines. + + +Aquiferous system +. Leuconoid. + + +Skeleton. +In cross section there is a thin cortical layer of triactines with long unpaired actines carried by a thick mass of tangentially arranged giant diactines. The choanosome is a mass of triactines traversed in places by short tracts of nail-shaped triactines. The atrial skeleton is a layer of tri- and tetractines with short unpaired actines and straight paired actines. + + +Spicules. +( +Figs 90b–g +) Giant diactines, nail-shaped triactines, large triactines with long unpaired actines, small tri- and tetractines with short unpaired actines. + + +Giant and smaller diactines ( +Figs 90b +), fusiform, curved, 105– +869 +– +2520 x +7.5– +37.1 +–84 µm. + + +Nail-shaped triactines ( +Figs 90c,c +1 +), fusiform, with one end poined and the opposite end with two tiny actines, usually more or less symmetrical; unpaired actine 252– +503 +–781 x 8.5– +9.9 +–12 µm, paired actines 3– +6.8 +– +15 x +2.5– +4.2 +–6 µm. + + +Triactines with long unpaired actines and flaring paired actines ( +Fig. 90d +); unpaired actines 292– +348 +–384 +x 10 +– +17.8 +–24 µm, paired actines 226– +297 +–342 +x 9 +– +18.4 +–23 µm. + + +Tetractines ( +Fig. 90e +), with short unpaired actines and straight paired actines; unpaired actines 31– +49 +– +61 x 8 +– +10.3 +–12 µm, paired actines 69– +192 +–231 +x 8 +– +11.6 +–14 µm, apical actines 3– +25 +– +32 x 3 +– +7.9 +–10 µm. + + +Triactines ( +Fig. 90f +), with short unpaired actines and straight paired actines; unpaired actines 30– +46 +– +63 x 7 +– +10.3 +–12 µm, paired actines 71– +188 +–234 +x 8 +– +10.9 +–12 µm. + + + + +Distribution and ecology. +Seychelles +, shallow-reef locality. + + + + +FIGURE 90. + +Kebira + +spec., ZMA Por. 10379b, from the Seychelles, a, habitus (scale bar = 1 cm), b–f, SEM images of the spicules, b, giant diactine, c, nail-shaped triactines, c1, details of nail-shaped triactines, d, large triactine with long unpaired actine, e, tetractine with short unpaired actine, f, triactine with short unpaired actine. + + + + +Remarks. +Although this specimen shares the possession of atrial tetractines with + +Kebira tetractinifera + + +sp.nov. + +, it shares also features with + +K. uteoides + +such as a dense layer of tangential diactines, twice as long as those of + +K. tetractinifera + + +sp.nov. + +Further research is necessary to establish the value of these features for distinction of additional taxa in + +Kebira + +. + +Unfortunately, our attempt to obtain a 28S sequence of the specimen failed. + + + \ No newline at end of file diff --git a/data/38/6C/C6/386CC616DCFEA5BEFF678917FB98FC74.xml b/data/38/6C/C6/386CC616DCFEA5BEFF678917FB98FC74.xml new file mode 100644 index 00000000000..6f0c8c20140 --- /dev/null +++ b/data/38/6C/C6/386CC616DCFEA5BEFF678917FB98FC74.xml @@ -0,0 +1,365 @@ + + + +Calcareous sponges of the Western Indian Ocean and Red Sea + + + +Author + +Van, Rob W. M. + + + +Author + +De, Nicole J. + +text + + +Zootaxa + + +2018 + +2018-06-01 + + +4426 + + +1 + + +1 +160 + + + +journal article +29979 +10.11646/zootaxa.4426.1.1 +cdd567ed-ebd8-4801-a6a4-af6c9fb964fd +1175-5326 +1271239 +18929E20-5296-4458-8A8A-4F5316A290FD + + + + + + + +Kebira tetractinifera + +sp.nov. + + + + +Figs 87a–d +, +88a–f +, +89a–e + + + + + + +Material +examined. + +Holotype +, +ZMA +Por. 15245, +South Africa +, +Port Elizabeth +, +Sea View +, +32.9333°S +27.7°E +, coll. +A. van Schie +, field nr. +UPES 96–074 +, + +6 February 1998 + +. + + + + +FIGURE 87. + +Kebira tetractinifera + + +sp.nov. + +from Eastern South Africa, a, habitus of holotype ZMA Por. 15245 (scale bar = 1 cm), b, habitus of paratype ZMA Por. 13952 (scale bar = 1 cm), c, detail of the same, d, light microscopic image of cross section of body wall of holotype. + + + + +FIGURE 88 +. + +Kebira tetractinifera + + +sp.nov +. + +, holotype ZMA Por. 15245, SEM images of sections of the skeleton, a, cross section of body wall, b, detail of cross section of peripheral skeleton (arrows: tracts of nail-shaped triactines), c, detail of the cross section of atrial skeleton, d, overview from above of peripheral skeleton, e, overview from above of atrial skeleton, f, detail of the atrial skeleton with protruding apical actines of the tetractines with short unpaired actines. + + + + +Paratype +, +ZMA +Por. 13952, +South Africa +, +Port Elizabeth +, +Cape +Recief, coll. +H. Engel +, + +20 November 1938 + + +. + + + + +Description. +A mass of upright tubular shapes, connected by flattened ridges. The +holotype +( +Fig. 87a +) is wet (alcohol preservation) and has a light beige color and a smooth surface. Size of the entire specimen is 3 + +x 2 x +2 + +cm, tubular individuals about +0.5 cm +diameter. The +paratype +( +Figs 87b–c +) is a dried tubular individual of +4 cm +high, pale yellow in color, with a broad base and a diameter of +1 cm +, with atrial wall +2 mm +thick and atrial cavity +5 mm +in diameter. Consistency firm to hard. + + +Aquiferous system +. Leuconoid. + + +Skeleton. +( +Figs 87d +, +88a–f +) In a cross section of the wall ( +Figs 87d +, +88a–c +), there is a cortical skeleton ( +Fig. 88d +) formed by triactines with longer unpaired actines, carried by the pointed ends of perpendicular giant diactines, with only few of the diactines in a tangential position. The choanosomal skeleton is a dense mass of large triactines partitioned off by giant diactines and thin tracts of nail-shaped triactines (arrows in +Fig. 88b +). The atrial skeleton is a layer of sagittal tri- and tetractines with short unpaired actines, with the apical actines of the tetractines protruding into the atrial cavity ( +Figs 88c,e–f +). + + + +FIGURE 89. + +Kebira tetractinifera + + +sp.nov. + +, holotype ZMA Por. 15245, SEM images of the spicules, a, giant and smaller diactines, b, nail-shaped triactines, b, details of nail-shaped triactines, c, triactines with long unpaired actines, d, triactine with short unpaired actine, e, tetractines with short unpaired actines. + + + +Spicules +. ( +Figs 89a–e +) Giant diactines, nail-shaped triactines, triactines with long unpaired actines, triactines with short unpaired actines, tetractines with short unpaired actines. + + +Giant and smaller diactines ( +Figs 89a +), fusiform, curved, 400– +904 +– +1380 x 15 +– +33.8 +–45 µm. + + +Nail-shaped triactines ( +Figs 89b,b +1 +), fusiform shaft, one end pointed, the opposite with conical or further extended short actines, arranged under a slight angle, often asymmetrical, unpaired actines 155– +249 +–352 x 7.5– +9.7 +–14 µm, paired actines 4– +14.5 +– +40 x 4 +– +7.5 +–12 µm. + + +Triactines with long unpaired actines ( +Figs 89c +), usually sagittal with paired actines similar in length or shorter, occasionally equiangular equiradiate; unpaired actines 156– +260 +–355 +x 10 +– +15.4 +–22 µm, paired actines 115– +182 +–256 +x 7 +– +14.2 +–20 µm. + + +Triactines with short unpaired actines and straight paired actines ( +Fig. 89d +); unpaired actines 49– +76 +–100 +x 8 +– +9.8 +–12 µm, paired actines 155– +169 +–195 x 7.5– +9.9 +–11 µm. + + +Tetractines with short unpaired actines and straight paired actines ( +Figs 89e +); unpaired actines 58– +82 +–115 +x 8 +– +9.1 +–10 µm, paired actines 126– +151 +–181 +x 7 +– +8.9 +–10 µm, apical actines 32– +43.6 +– +50 x 6 +– +7.6 +–10 µm. + + + + +Distribution and ecology. +Port Elizabeth region, +Eastern + +South +Africa + +, in shallow water. + + + + +Etymology. +The name reflects the presence of sagittal tetractines, a feature distinguishing the new species from the +type +species, + +K. uteoides + +. + + + + +Remarks. +The possession of tetractines is the defining character of the new species, but the diactines differ from + +K. uteoides + +in being shorter and thinner and not forming a thick cortical layer. Less definite is the difference in thickness of the triactines with long unpaired actines, with those of + +K. uteoides + +being measurably thinner. See also below in the description of the +Seychelles + +Kebira + +specimen. + + +We obtained partial 28S sequences for the two +Red Sea +specimens of + +K.uteoides + +and the +holotype +of + +K. tetractinifera + + +sp.nov +. + +They grouped together in our Phylogeny of +Fig. 3 +with a high bootstrap value (94%). A separately investigated trimmed alignment of these three sequences, totaling 400 sites, showed four site differences between the two identical + +K. uteoides + +sequences and the sequence of the new species. + + + + \ No newline at end of file diff --git a/data/38/6C/E9/386CE9587FBAEF7FBC62FF57811AF0FF.xml b/data/38/6C/E9/386CE9587FBAEF7FBC62FF57811AF0FF.xml new file mode 100644 index 00000000000..52efc19e14f --- /dev/null +++ b/data/38/6C/E9/386CE9587FBAEF7FBC62FF57811AF0FF.xml @@ -0,0 +1,254 @@ + + + +An illustrated catalogue of Rudolf Sturany's type specimens in the Naturhistorisches Museum Wien, Austria (NHMW): Red Sea gastropods + + + +Author + +Albano, Paolo G. +https://orcid.org/0000-0001-9876-1024 +Department of Palaeontology, University of Vienna, Althanstrasse 14, 1090 Vienna, Austria +pgalbano@gmail.com + + + +Author + +Bakker, Piet A. J. +Naturalis Biodiversity Center, Darwinweg 2, 2333 CR Leiden, The Netherlands + + + +Author + +Janssen, Ronald +Malacology Section, Senckenberg Research Institute and Natural History Museum, Senckenberganlage 25, 60325 Frankfurt am Main, Germany, + + + +Author + +Eschner, Anita +Naturhistorisches Museum Wien, 3. Zoologische Abteilung, Burgring 7, 1010 Wien + +text + + +Zoosystematics and Evolution + + +2017 + +2017-01-18 + + +93 + + +1 + + +45 +94 + + + + +http://dx.doi.org/10.3897/zse.93.10039 + +journal article +http://dx.doi.org/10.3897/zse.93.10039 +1860-0743-1-45 +0BA1B8432BD449FC8FDAF68041A5D167 +8BF19C7ACDA45671A0A8BCF324660CD0 +250941 + + + + +Nassa munda Sturany, 1900 +Figure 13 + + + + +Nassa munda +Sturany, 1900a: 200; redescribed and illustrated in +Sturany (1903) +, page 223-224, plate II, figures 4a-b. + + + +Type locality. + +Station 135, +"suedoestlich +von Akik Seghir" [south-east of Akik Seghir, Eritrea], +17°26.1'N +, +39°19'E +, 332m. + + + +Additional original localities. + +Station 135 (332 m) and 145 (800 m) (Southern Red Sea; Table +1 +). + + + +Type material. + +Figured syntype: NHMW 84190 (station 135; height: 9.9 mm; figured in +Sturany 1903 +, plate II, figures 4a-b). Further syntypes: NHMW 71640/O/746 (station 135): 4 specimens; NHMW 84191 (station 135): 14 specimens; NHMW 84192 (station 145): 1 specimen. + + + +Additional material. + +NHMW 84193 (station 170): +1 specimen +. + + + +Original description. + + +Gehaeuse +klein und festschalig, kegelig-oval; von den acht +Umgaengen +sind die ersten gerundet und glatt, die +uebrigen +stufig abgesetzt und mit zahlreichen +Querwuelsten +(etwa 26 auf der Schlusswindung) ausgestattet, die von Spiralstreifen gekreuzt und gekerbt werden. Auch ist durch eine +schaerfer +eingegrabene Spirallinie der oberste Theil jeder Windung als eine Reihe von +Hoeckerchen +abgesetzt. Auf dem +Aussenrande +der +Muendung +in der Regel sechs bis acht +Zaehnchen +, von denen einige besonders hervortreten +koennen +. Andeutung von +Baenderung +nur selten zu beobachten. + + + + +Hoehe +der Schale 7 1/2 bis 9 3/4, Breite 4 1/4 bis 5 mm; +Hoehe +der +Muendung +3 1/2 bis 4 1/2, Breite derselben 2 bis 2 3/4 mm. + + + +Von Station 135 (332 m) und 145 (800 m) vorliegend. + + + +Figure 13. + +Nassa munda + +Sturany, 1900, Station 135 (Akik Seghir, Eritrea, Red Sea). +A-C, E +. Figured syntype, NHMW 84190: front ( +A +), right side ( +B +), back ( +C +), protoconch ( +E +). +D +. Original figure by +Sturany (1903) +. +F +. Original label of figured syntype. Scale bars: +A-C +: 2 mm, +E +: 0.2 mm. + + + + +Translation. +Shell small and thick, conical-oval; of the eight whorls, the first are rounded and smooth, the other scalariform with numerous axial ribs (about 26 on the last whorl) which are crossed and notched by spiral threads. The uppermost part of each whorl bears a strongly sculptured spiral cord with a series of tubercles. On the outer edge of the mouth, there are usually six to eight teeth, some of which may be particularly prominent. Traces of colour bands can rarely be observed. +Height of the shell 7.5 to 9.75, width 4.25 to 5 mm; height of the mouth 3.5 to 4.5, width 2 to 2.75 mm. +From station 135 (332 m) and 145 (800 m). + + +Comments. + +Cernohorsky (1984 +: 156) listed + +munda + +as +nomen dubium +and possible synonym of +Nassarius (Zeuxis) idyllius +(Melvill & Standen, 1901). + + + +Nassa lathraia + +as well as + +Nassa sporadica + +, + +Nassa stiphra + +and + +Nassa munda + +are published at the same date and are regarded synonymous. Examination of the type material as well as of rich material from various expeditions to the deep Red Sea (RJ) shows that the various names only denote sculptural variants which can be observed to occur together in part at the same stations and which cannot be told apart as different taxa. Whereas Janssen in +Janssen and Taviani (2015) +used + +lathraia + +as valid name, +Dekker and Orlin (2000 +: 28) should be regarded as first revisers who selected + +Nassarius mundus + +(Sturany, 1900) as valid name for the taxon explicitly denoting the other names as synonyms. +Cernohorsky (1984 +: 103) regarded + +lathraia + +as a possible synonym of +Nassarius (Niotha) sinusigerus +(A. Adams, 1852). Whether this is correct needs further study and comparison of many other conchologically similar species. If it proves correct, + +sinusigerus + +would become the valid name for this assemblage of forms denoted by Sturany with four names. + + + + \ No newline at end of file diff --git a/data/38/6C/F9/386CF993C96B5180A325C596FD3A4E05.xml b/data/38/6C/F9/386CF993C96B5180A325C596FD3A4E05.xml new file mode 100644 index 00000000000..b6a7515eff1 --- /dev/null +++ b/data/38/6C/F9/386CF993C96B5180A325C596FD3A4E05.xml @@ -0,0 +1,192 @@ + + + +Two new genera and eight new species of jumping spiders (Araneae, Salticidae) from Xishuangbanna, Yunnan, China + + + +Author + +Lin, Yejie +Hebei Key Laboratory of Animal Diversity, College of Life Science, Langfang Normal University, Langfang 065000, China +https://orcid.org/0000-0002-6789-2731 + + + +Author + +Li, Shuqiang +Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China +https://orcid.org/0000-0002-3290-5416 +lisq@ioz.ac.cn + +text + + +ZooKeys + + +2020 + +952 + + +95 +128 + + + + +http://dx.doi.org/10.3897/zookeys.952.51849 + +journal article +http://dx.doi.org/10.3897/zookeys.952.51849 +1313-2970-952-95 +B06E0C6B6A964AEA8BE1D121929504FD +835A323141EB524086056EB62986585C + + + + +Foliabitus weihangi +sp. nov. +Figures 7 +, 8 + + + +Type material. + +Holotype +♂(IZCAS-Ar40399), China: Yunnan: Xishuangbanna, Mengla County, Menglun Township, XTBG, Leprosy Village, +21.8932N +, +101.2883E +, elevation ca 550 m, 09.V.2018, Weihang Wang leg. +Paratypes +4♂4♀ (IZCAS-Ar40400-Ar40407), China: Yunnan: Xishuangbanna, Mengla County, Menglun Township, XTBG, Leprosy Village, +21.8986N +, +101.2683E +, elevation ca 523 m, 29.IV.2019, Zilong Bai leg. + + + +Etymology. +The species is named after Mr. Weihang Wang, who has helped us greatly with this research; noun (name) in genitive case. + + +Diagnosis. + + +Foliabitus weihangi + +sp. nov. resembles + +F. scutigerus + +(Zabka, 1985) and + +F. longzhou + +Zhang & Maddison, 2012 by the long and coiled embolus, nearly forming a circle, but differs in the following: the RTA is curved towards the bulb medially in ventral view (vs. the RTA straight in ventral view in + +F. scutigerus + +and + +F. longzhou + +); the RTA curved without a small cusp distally (vs. with a small cusp distally in + +F. longzhou + +), the tegular lobe protrudes from the bulb (vs. indistinct in + +F. scutigerus + +and + +F. longzhou + +); in the female, the copulatory ducts are S-shaped (vs. C-shaped in + +F. longzhou + +). + + + +Description. + +Male +(Figs +7A-C +, +8C, G +). Total length 4.29. Carapace 1.94 long, 1.61 wide. Abdomen 2.35 long, 1.18 wide. Clypeus 0.05 high. Eye sizes and inter-distances: AME 0.43, ALE 0.27, PLE 0.25, AERW 1.34, PERW 1.26, EFL 1.02. Legs: I 7.25 (2.13 + 2.88 + 1.47 + 0.76), II 5.14 (1.66 + 1.78 + 1.10 + 0.60), III 5.50 (1.76 + 1.80 + 1.38 + 0.56), IV 5.61 (1.66 + 1.92 + 1.53 + 0.50). Carapace black, cephalic part with dense, green scale-like setae around eyes. Fovea longitudinal, posterior to PLEs. Clypeus yellow, covered with dense, white setae. Chelicerae black, with two retromarginal teeth and one promarginal tooth. Endites and labium dark brown. Sternum brown, covered with dark setae. Legs pale yellow, except leg I black, covered with long, dark setae. Abdomen elongated oval, dorsum black, with pale pattern; venter black with dark setae. + + + +Figure 7. +Palp of + +Foliabitus weihangi + +sp. nov., male holotype. +A +prolateral +B +ventral +C +retrolateral. + + + +Palp (Fig. +7A-C +): Patella red-brown, almost as long as wide; tibia stocky, slightly wider than long, with sclerotized, hook-shaped RTA, curved towards the bulb; cymbium longer than wide, covered with long setae; bulb longer than wide, tegular lobe distinct, curved retrolaterally; embolus long and coiled, nearly forming a circle. + + +Female +(Fig. +8A, B, D-F +). Total length 4.82. Carapace 2.04 long, 1.63 wide. Abdomen 2.78 long, 1.60 wide. Clypeus 0.06 high. Eye sizes and inter-distances: AME 0.47, ALE 0.28, PLE 0.27, AERW 1.29, PERW 1.26, EFL 1.12. Legs: I 6.16 (1.96 + 2.43 + 1.16 + 0.61), II 5.00 (1.53 + 1.96 + 1.01 + 0.50), III 5.10 (1.59 + 1.66 + 1.31 + 0.54), IV 5.71 (1.66 + 1.98 + 1.53 + 0.54). Habitus (Fig. +8D +) similar to that of male except paler. Abdomen dorsally whitish with black pattern similar to male, ventrally pale yellow, with small black triangular patch near spinnerets. + + +Epigyne (Fig. +8A, B +) wider than long, windows large, separated by median septum; copulatory openings at center of windows; copulatory ducts long, S-shaped; spermathecae oval; fertilization ducts well-developed, membranous, lamellar. + + + +Distribution. +Known only from the type locality in Yunnan, China. + + +Figure 8. + +Foliabitus weihangi + +sp. nov., female paratype and male holotype. +A +epigyne, ventral +B +vulva, dorsal +C +male holotype habitus, dorsal +D +female paratype habitus, dorsal +E +same, ventral +F +prolateral view of right leg I, female paratype +G +prolateral view of right leg I, male holotype. + + + + + \ No newline at end of file diff --git a/data/38/6D/21/386D2161DE59FFE7FF757748DEE2AEF8.xml b/data/38/6D/21/386D2161DE59FFE7FF757748DEE2AEF8.xml new file mode 100644 index 00000000000..b4daf04364c --- /dev/null +++ b/data/38/6D/21/386D2161DE59FFE7FF757748DEE2AEF8.xml @@ -0,0 +1,456 @@ + + + +Description a new species of the genus Orphnebius Motschulsky, 1858 (Coleoptera: Staphylinidae: Aleocharinae) from Xizang, China + + + +Author + +Jiang, Ri-Xin +maoshuwuyouzhi @ 163. com; https: // orcid. org / 0000 - 0002 - 5339 - 853 X + + + +Author + +Li, Bo-Yan +Institute of Entomology, Guizhou University, Guizhou Provincial Key Laboratory for Agricultural Pest Management of the Mountainous Region, Guiyang, 550025, P. R. China. + + + +Author + +Wang, Shuo + +text + + +Zootaxa + + +2020 + +2020-06-12 + + +4790 + + +3 + + +593 +599 + + + +journal article +10.11646/zootaxa.4790.3.13 +1175-5326 +3891267 +AC939AA2-D8D6-4F5A-85A8-6DE7B316FC09 + + + + + + + +Orphnebius lilizheni + +sp. nov. +Jiang, Li & Wang sp. nov. ÷KHẘDaem + + + + + + +( +Figs. 1–4 +) + + + + +Type material (9 exs, +3 ♂♂ +, +6 ♀♀ + +). +Holotype +: + + + +CHINA +: + + +, labeled + +‘ + +China +: +Xizang +, +Linzhi City +( +ẇźṃ +), +Milin County +( +*ẇu +), +Nanyigou +( +ṁDzḿ +), H: + +3166 m + +, + +19.VII.2019 + +, +Li Bo-yan +leg., in nest of + +Tetraponera + +sp.’ ( +SHNU +) + +. + + +Paratypes +: +CHINA +: + +2 ♂♂ +, +6 ♀♀ +. +Same +label data as the holotype ( +1 ♂ +, +2 ♀♀ +SHNU +; +1 ♂ +, +4 ♀♀ +GUGC +) + +. + + + + +FIGURE 1. +Habitus of + +Orphnebius lilizheni + + +sp. nov. +A. + +Male; +B. +Female. + + + + +Description. +Male ( +Figs 1A +, +2 +A–B, D–H, K–M). Body bicolourable, head, pronotum and elytra black, abdomen brown, dorsal surface shiny and without punctures. + + +Head ( +Fig. 2A +) slightly wider than long, shiny and covered with sparse long hairs. Antenna ( +Fig. 2B +) moderately long and apically asymmetric; antennomere I–V longer than wide, I expanded near apex; II about as long as IV; III long, about 1.5 times as long as II; V shorter than IV; VI about as long as wide; VII–X similar, obviously wider than long, VII–X similar, obviously wider than long; XI of ovoid shape and approximately as long as the combined length of IX–X. + + +Pronotum ( +Fig. 2A +), about 1.4 times as wide as long; dorsal surface shiny and without punctures and pubescence; lateral margins with several long hairs. + +Elytra wider than long; near trapezoid shape; dorsal surface shiny, covered with sparse hairs and small punctures; lateral margins with erect long black hairs. Hind wings present. +Legs simple. All femora black, without modification. Tibiae dark brown, protibiae covered with very dense short hairs, and mesotibiae and metatibiae covered with much sparse short hairs. + +Abdominal segments III–VIII reddish brown, III–VII with weakly tapering posteriad, III widest. Posterior margin of tergites III–VI with moderately long black hairs. Tergite VII weakly impressed and in basal 1/3 with transverse row of regular striae, posterior margin of tergite VII with pronounced palisade fringe. Tergite VIII ( +Fig. 2E +) transverse with convex posterior margins and covered with sparse strong setae. Sternite VIII ( +Fig. 2D +) with sparse long setae at posterior margin. IX–X ( +Figs 2 +G–H) strongly modified, covered with dense and long hairs + + + +FIGURE 2. +Diagnostic features of + +Orphnebius lilizheni + + +sp. nov. +A. + +Head and pronotum, in dorsal view; +B. +Antenna; +C. +Spermathecal; +D. +Sternite VIII; +E. +Tergite VIII; +F. +Paramere; +G. +Male segments IX–X, dorsal view; +H. +Same, ventral view; +I. +Female segments IX–X, dorsal view; +J. +Same, ventral view; +K. +Media lobe of aedegus, ventral view; +L. +Same, lateral view; +M. +Same, dorsal view. + + + +Media lobe of aedeagus broad and short ( +Figs 2 +K–M). Paramere small in relation to median lobe, apical truncate, with two short setae ( +Fig. 2F +). + + +Measurements. AnL +1.88–1.94 mm +, BL +4.94–5.04 mm +, HL +0.81–0.84 mm +, HW 0.99–1.00 mm, PL +0.78–0.80 mm +, PW +1.14–1.17 mm +, EL +0.76–0.77 mm +, EW +1.88–1.93 mm +, AL +2.58–2.63 mm +, AW +1.83–1.88 mm +, Adl +1.29 mm +. + + +Female ( +Figs 1B +, +2C +, I–J) generally similar to male, usually slightly larger. Segments IX–X ( +Figs 2 +I–J) distinctly modified, with long and dense setae; spermathecal ( +Fig. 2C +) duct simply bent, proximally straight, neither twisted nor undulate. + + + +FIGURE 3. A. +Larva of + +Orphnebius lilizheni + + +sp. nov. + +, dorsal view; +B. +Same, lateral view; +C. +Same, ventral view; +D. + +Myrmica + +sp., dorsal view; +E. +Same, lateral view; +F. +Larva of + +Myrmica + +sp. + + + +Measurements. AnL +1.90–1.95 mm +, BL 5.00– +5.17 mm +, HL +0.81–0.84 mm +, HW 1.00– +1.03 mm +, PL +0.80–0.82 mm +, PW +1.16–1.19 mm +, EL +0.76–0.79 mm +, EW +1.88–1.95 mm +, AL +2.63–2.73 mm +, AW +1.83–1.93 mm +. + + +Larvae ( +Figs 3 +A–C, third instar), ivory-white, fat, soft and much weakly osteogenated, more or less resembling the larvae of + +Myrmica + +sp ( +Fig. 3F +). + + + +FIGURE 4. +Habitat of + +Orphnebius lilizheni + + +sp. nov. +A. + +Adults and larvae in a nest of + +Myrmica + +sp.; +B. +A + +Myrmica + +sp. ant in nest; +C. +General environment of the type locality: Baotianman (Xizang, China). Laa—Larva of the host ant; La—Larva of + +Orphnebius lilizheni + + +sp. nov. + +; ad—Adults of + +Orphnebius lilizheni + +sp. nov. + + + +Comparative Notes. +The new species is similar to + +Orphnebius longistriatus +Assing, 2006 + +and + +O. hamatus +Assing, +2006 + +in general appearance. But + +O. lilizheni + + +sp. nov. + +has concolorous abdominal segments, while the abdominal segments III–V, VI and VII–VIII are respectively blackish, brown and reddish in + +O. longistriatus + +. The new species can be distinguished from + +O. hamatus + +by the different form of median lobe of aedeagus. + +O. hamatus + +possess a very large median lobe, and the ventral process is short, broad and apically curved, while the median lobe of the new species is simple and short, and the ventral process of the new species is more strongly curved. The paramere of + +O. hamatus + +has four long and two short setae while the new species with only two long setae. + + + + +Distribution. +China +: +Xizang +. + + +Biological notes. +The adults and larvae of this new species were collected in a nest of + +Myrmica + +sp. ( +Figs 4 +A–B). + + + + +Etymology. +This species is named in honor of Prof. Li-Zhen Li ( +Shanghai +Normal University, +Shanghai +, +China +), a famous Chinese insect taxonomist, who works on the Staphylinid beetles for a long time. + + + + \ No newline at end of file diff --git a/data/38/6D/3A/386D3A9FAEAE9761E1ACC14BF0676383.xml b/data/38/6D/3A/386D3A9FAEAE9761E1ACC14BF0676383.xml new file mode 100644 index 00000000000..f60b04c4dde --- /dev/null +++ b/data/38/6D/3A/386D3A9FAEAE9761E1ACC14BF0676383.xml @@ -0,0 +1,172 @@ + + + +Beitrag zur Kenntnis der Höhlen-Oribatiden der Schweiz (Acari: Oribatida) (Neue und interessante Milben aus dem Genfer Museum LI) + + + +Author + +Mahunka, S. + +text + + +Revue suisse de Zoologie + + +1993 + +100 + + +225 +233 + + + + +http://unknown + +journal article +ORI6235 + + + + +Octodurozetes berndhauseri +sp. n. + + + + +Dimensionen. - +Laenge +: 553 +ym +, Breite: 338 +ym +. + + +Integument: Cerotegumentale Schicht fehlt. Das cuticulare Ornament (Foveolen) ist auf dem vorderen Teil des Notogasters und auf der ventralen Platte stark +ausgepraegt +, es wird nach hinten +allmaehlich +schwaecher +. Cuticula des +Koerpers +schwach punktiert oder ornamentiert mit Foveolen. Einige feine Runzeln laufen parallel mit dem Seitenrand der Pteromorphen. Auf dem Femur der II.-IV. Beine einige sich +annaehernde +Linien vorhanden. + + +Prodorsum: Rostrum einheitlich. Die Lamellen sind stark, scharf +kielfoermig +, am Rostrum sie sind gut sichtbar in Dorsalansicht (Abb. 5). Sie verschmelzen +allmaehlich +mit der Prolamelle und biegen bei den Rostralborsten in Richtung des Mentums ab. Sublamelle ebenfalls gut entwickelt (Abb. 7), Area porosa lamellaris (Al) liegt tangential. Translamelle und Cuspides der Lamellen fehlen, aber eine feine transversale Linie vor den Lamellarborsten sichtbar. Tutorium eindeutig gut entwickelt, aber seine Cuspis fehlt. Alle Borsten des Prodorsums (Abb. 9) lang und bewimpert, die Spitzen der Rostral- und Lamellarborsten laufen sehr fein aus, die Interlamellarborsten sind stumpfer als die +uebrigen +. Die Rostral- und Lamellarborsten stehen ausserhalb der Lamellen. Sensillus mit kleinen und +duennen +Doernchen +einseitig besetzt (Abb. 7). Exobothridialborste +duenn +und glatt. + + + +Abb +. 5-8. + + +Octodurozetes berndhauseri +gen. n. +, +sp. n. +- 5: Dorsalansicht, 6: Ventralansicht, 7: Podosoma in Seitenansicht, 8: Trichobothrium. + + + + +Abb +. 9-14. + + +Octodurozetes berndhauseri +gen. n. +, +sp. n. +- 9: Lamellarregion in Laterodorsalansicht, 10: +Koerperende +in Seitenansicht, 11: Tibia I in Dorsalansicht, 12: Genu, Tibia und Tarsus von Bein I, 13: Femur II, 14: Femur I. + + + +Notogaster +: Pteromorpha gross, +zungenfoermig +. Durch die Form des Notogasters ist diese Art gut gekennzeichnet, die dorsosejugale Sutur ist konvex, der Hinterrand des Notogaster ist geradlinig (Abb. 5) und reicht +ueber +die Ventralplatte hinaus (Abb. 10). Auf dem Notogaster befinden sich 10 Paar Borsten, alle sind kurz und glatt. Es sind 4 Paar Areae porosae zu erkennen, alle +ungefaehr +gleich gross, die A1 liegen in der Mitte des Notogasters nahe beieinander. Von den 5 Paar Lyrifissuren sind nur zwei Paar (ih, ips) in der Seitenansicht sichtbar, ip steht ziemlich weit vom hinteren Seitenrand entfernt. + +Seitenregionen des Podosoma: Pedotectum 1 sehr niedrig, Discidium mit eingebuchtetem Hinterrand. Die Carina circumpedalis ist lang und erreicht den Rand der Ventralplatte. + +Ventralseite (Abb. 6): Von den Apodemen sind Ap. sej. und Ap. 3 vor der Genitalklappe miteinander verschmolzen, die +uebrigen +kurz oder reduziert. Epimeralborstenformel: 3-1-3-3, alle Borsten sind fein und schwer zu erkennen. In der Anogenitalregion befinden sich 5 Paar Genital, 1 Paar Aggenital-, 2 Paar Anal- und 3 Paar Adanalborsten. Die Borsten adj entspringen in preanaler Position, die Lyrifissuren iad liegen in der vorderen Ecke der Analklappen. + + +Beine: Tarsus und Tibia (Abb. 12) der ersten Beines mit +laenglichem +Kamm. Solenidia von Tibia I entspringen auf einer langen, starken Apophysis, phi2 in anterolateraler Position (Abb. 11). Femora der Beine II (Abb. 13) und III blattartig verbreitet. Borstenformel der Beine: + +I: 1 - 5 - 3+1 - 4+2 - 20+2 - 1 +IV: 1 - 2 - 2 - 3+1 - 12 - 1. + + + +Untersuchtes Material: + +Holotypus +: +SUISSE +( +Valais +), +Vouvry +(environ +7 km +de l'embouchure du Rhone dans le Lac +Leman +): + +Grotte de la Pierre +a +Perret + +(VS 13), + +490 m +. + +, + +10.VIII.1989 + +, leg. +B. Hauser +. + + + + +Bemerkungen: Siehe die Beschreibung der neuen Gattung. + + +Derivatio nominis: Ich widme die neue Art meinem guten Freund, Dr. Bernd Hauser, Konservator am Naturhistorischen Museum Genf. + + + \ No newline at end of file diff --git a/data/38/6D/53/386D534329DAB8185950F8EBE6CE3489.xml b/data/38/6D/53/386D534329DAB8185950F8EBE6CE3489.xml new file mode 100644 index 00000000000..ce3b363fd85 --- /dev/null +++ b/data/38/6D/53/386D534329DAB8185950F8EBE6CE3489.xml @@ -0,0 +1,49 @@ + + + +Voyage de M. E. Simon dans l'Afrique australe (janvier-avril 1893). 3 e mémoire. Formicides. + + + +Author + +Emery, C. + +text + + +Annales de la Société Entomologique de France + + +1895 + +64 + + +15 +56 + + + + +http://antbase.org/ants/publications/3788/3788.pdf + +journal article +3788 + + + + +Var. obscurata +, +n. var. + + + +- Je fonde cette variete sur deux vieux exemplaires [[ worker ]] de ma collection, etiquetes Cap de Bonne-Esperance. Ils different du type par la couleur qui est brun ferrugineux, avec le devant de la tete, l'abdomen et les membres roux clair. L'arete laterale du dos du thorax est moins vive en arriere. Les yeux sont situes un peu moins en arriere que chez le type. + + +S. Mocquerysi Er. Andre offre quelque ressemblance avec cette espece, dont il differe, toutefois, par le 1 er segment du pedicule abdominal non borde d'aretes et par sa couleur. + + + \ No newline at end of file diff --git a/data/38/6D/8D/386D8D13A999503092E191775FAACF6F.xml b/data/38/6D/8D/386D8D13A999503092E191775FAACF6F.xml new file mode 100644 index 00000000000..ad07e70b547 --- /dev/null +++ b/data/38/6D/8D/386D8D13A999503092E191775FAACF6F.xml @@ -0,0 +1,162 @@ + + + +? An illustrated catalogue of the type specimens of Lepidoptera housed in the Zoological Museum Hamburg (ZMH): Part II. superfamily Papilionoidea + + + +Author + +Zahiri, Reza +https://orcid.org/0000-0001-6274-6973 +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany & Canadian Food Inspection Agency, Ottawa Plant Laboratory, Entomology Unit, Bldg. 18, 960 Carling Ave., K 1 A 0 C 6, Ottawa, Ontario, Canada +reza.zahiri@gmail.com + + + +Author + +Nazari, Vazrick +https://orcid.org/0000-0001-9064-8959 +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany + + + +Author + +Rajaei, Hossein +https://orcid.org/0000-0002-3940-3734 +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany + + + +Author + +Wiemers, Martin +https://orcid.org/0000-0001-5272-3903 +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany + + + +Author + +Fatahi, Maryam +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany + + + +Author + +Seidel, Matthias +https://orcid.org/0000-0002-4913-8778 +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany + + + +Author + +Dalsgaard, Thure +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany + + + +Author + +Husemann, Martin +https://orcid.org/0000-0001-5536-6681 +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany + +text + + +Evolutionary Systematics + + +2021 + +2021-08-20 + + +5 + + +2 + + +193 +261 + + + + +http://dx.doi.org/10.3897/evolsyst.5.63435 + +journal article +http://dx.doi.org/10.3897/evolsyst.5.63435 +2535-0730-2-193 +984E15D880E04B7DA84F92BB0AD4EA73 +21773559522D5D9DA4B1A7DA51E4F2A6 + + + + +65. +Pieris r. exigua Verity, 1923 + + + +Original combination. + +" +Pieris ergane +, H.-G. race exigua, mihi." Verity, 1923 Ent. Rec. 35 Suppl. (18). + + + +Current combination. + + + +Pieris ergane + +r. exigua Verity, 1923 + +. + + + +Current status. +Infrasubspecific and hence unavailable name. + + +Original material. + +Labelled as +"Cotype" +2?? (ZMH 835577-835578) (Fig. +65 +). "exigua Vrty" // "Marche / Bolognola / 7 Ag 1937 / Querci" // [blank label] // "ZMH 835577"; "exigua Vrty" // "Marche / Bolognola / 8 Ag 1937 / Querci" // [blank label] // "ZMH 835578". + + + +Original locality. +Italy: "Upper Fargno Valley, at 1400 m., in the Sibillini Mts." + + +Remarks. + +Verity (1923) proposed this name as a race of + +P. ergane + +(Geyer, 1828). According to +Kudrna (1983) +, this name in unavailable because it is a seasonal form and also a nomen nudum. The year on the specimen labels (1937) indicate specimens were collected 14 years after description (1923) from the same location the original holotype material was collected. As a result, the black label of the specimens treated as +"types" +is erroneous. The specimen collected from the same geographical location from which the type specimen was collected is called topotype. According to ICZN (1999), a topotype has no formal standing and is not regulated by the Code. Therefore, these two specimens are erroneously labelled as types, should be annotated as "Not a Type" and are treated here as +"Non-type" +specimens. + + + + \ No newline at end of file diff --git a/data/38/6D/90/386D90B5C9C71FD2E1603F39FA43EFE9.xml b/data/38/6D/90/386D90B5C9C71FD2E1603F39FA43EFE9.xml new file mode 100644 index 00000000000..43b6eb71404 --- /dev/null +++ b/data/38/6D/90/386D90B5C9C71FD2E1603F39FA43EFE9.xml @@ -0,0 +1,100 @@ + + + +New Staphylinidae (Coleoptera) records with new collection data from New Brunswick, Canada: Paederinae + + + +Author + +Webster, Reginald P. + + + +Author + +DeMerchant, Ian + +text + + +ZooKeys + + +2012 + +186 + + +273 +292 + + + + +http://dx.doi.org/10.3897/zookeys.186.2504 + +journal article +http://dx.doi.org/10.3897/zookeys.186.2504 +1313-2970-186-273 + + + + +Lathrobium (Lathrobium) simile LeConte, 1863 +Map 5 + + + +Material examined. + +Additional New Brunswick records, Carleton Co., Hovey Hill P.N.A., +46.1115°N +, +67.7770°W +, 10.V.2005, R. P. Webster, hardwood forest, in moist leaf litter and moss near forest pool (1 ♂, RWC); Meduxnekeag Valley Nature Preserve, +46.1956°N +, +67.6803°W +, 15.IX.2004, R. P. Webster, mixed forest, in decaying fungi (1 ♂, RWC); same locality, forest type and collector but +46.1976°N +, +67.6850°W +, 4.V.2006, R. P. Webster, margin of vernal pond, in moist leaf litter (1 ♂, RWC); Jackson Falls, Bell Forest, +46.2210°N +, +67.7210°W +, 11.V.2005, M.-A. +Giguere +& R. Webster, hardwood forest, in leaf litter near small brook (1 ♂, 2 ♀, RWC). Sunbury Co., Acadia Research Forest, 30.VI.1999, G. Gesner, Strip Cut 8, Site 1, pitfall trap (1, AFC); Acadia Research Forest, +45.9799°N +, +66.3394°W +, 18.VI.2007, R. P. Webster, mature red spruce and red maple forest, sifting leaf litter (1 ♂, 1 ♀, RWC). + + + +Map 5. Collection localities in New Brunswick, Canada of +Lathrobium simile +. + + + + +Collection and habitat data. +Adults of this species were found in hardwood forests, mixed forests, and a mature red spruce forest. Adults were collected from moist leaf litter near forest pools or vernal ponds, near a small brook, and from the forest floor. One individual was collected from decaying fungi on the forest floor. This species was collected during May, June, and September. + + +Distribution in Canada and Alaska. + +MB, ON, QC, NB, NS ( +Campbell and Davies 1991 +; +Klimaszewski et al. 2005 +). This species was first reported from New Brunswick by +Klimaszewski et al. (2005) +from the Acadia Research Forest. + + + + \ No newline at end of file diff --git a/data/38/6D/BC/386DBCF976471E455C9801EF98F37C87.xml b/data/38/6D/BC/386DBCF976471E455C9801EF98F37C87.xml new file mode 100644 index 00000000000..dc686637e85 --- /dev/null +++ b/data/38/6D/BC/386DBCF976471E455C9801EF98F37C87.xml @@ -0,0 +1,112 @@ + + + +A cybercatalogue of American sand fly types (Diptera, Psychodidae, Phlebotominae) deposited at the Natural History Museum, London + + + +Author + +Adams, Zoe J. O. + + + +Author + +Shimabukuro, Paloma Helena Fernandes + +text + + +Biodiversity Data Journal + + +2018 + +6 + + +24484 +24484 + + + + +http://dx.doi.org/10.3897/BDJ.6.e24484 + +journal article +http://dx.doi.org/10.3897/BDJ.6.e24484 +1314-2828--24484 + + + + +Dampfomyia rosabali Fairchild & Hertig, 1956 + + + + +Phlebotomus rosabali +Fairchild & Hertig, 1956 ( +Fairchild and Hertig 1956 +) + + + +Materials + + +Type status: +Paratype +. Occurrence: catalogNumber: +BMNHE1721991 +; sex: +Female +; Taxon: scientificName: Dampfomyia (Dampfomyia) rosabali (Fairchild & Hertig, 1956); Location: country: +Costa Rica +; stateProvince: Puntarenas; locality: +Barranca, Finca Socorrito +; Event: eventDate: +12-17-51 +; eventRemarks: http://phlebotominaenhmtypes.myspecies.info/node/110; Record Level: institutionCode: +NHMUK +; basisOfRecord: Preserved Specimen + + +Type status: +Paratype +. Occurrence: catalogNumber: +BMNHE1722048 +; sex: +Male +; Taxon: scientificName: Dampfomyia (Dampfomyia) rosabali (Fairchild & Hertig, 1956); Location: country: +Colombia +; stateProvince: Cauca; municipality: +Bolivar +; locality: + +Bolivar +(Cauca) + +; Event: eventDate: +23/01/44 +; eventRemarks: http://phlebotominaenhmtypes.myspecies.info/node/167; Record Level: institutionCode: +NHMUK +; basisOfRecord: Preserved Specimen + + + + +Distribution +Colombia, Costa Rica, Panama + + +Notes + +Valid species in +Dampfomyia (Dampfomyia) +. + + + + \ No newline at end of file diff --git a/data/38/6D/E3/386DE3246F285E078E877DF30A7CF171.xml b/data/38/6D/E3/386DE3246F285E078E877DF30A7CF171.xml new file mode 100644 index 00000000000..d4ec72ed21d --- /dev/null +++ b/data/38/6D/E3/386DE3246F285E078E877DF30A7CF171.xml @@ -0,0 +1,70 @@ + + + +Catalogue of Geadephaga (Coleoptera, Adephaga) of America, north of Mexico + + + +Author + +Bousquet, Yves +Agriculture and Agri-Food Canada, Central Experimental Farm, Ottawa, Ontario, Canada +bousquety1@yahoo.com + +text + + +ZooKeys + + +2012 + +2012-11-28 + + +245 + + +1 +1722 + + + + +http://dx.doi.org/10.3897/zookeys.245.3416 + +journal article +http://dx.doi.org/10.3897/zookeys.245.3416 +1313-2970-245-1 +FFFF52503A0AFF882450FFB66D45FF8E +578462 + + + + +Cicindela willistoni hirtifrons Willis, 1967 + + + + +Cicindela willistoni hirtifrons +Willis, 1967: 301. Type locality: "Big Salt Marsh, 11 mi[les] N[orth]E[ast] of Hudson, Stafford Co[unty], Kansas" (original citation). Holotype (♂) in SMEK. + + + +Distribution. + +This subspecies, the "Hairy-fronted Tiger Beetle", is found in central Kansas, western Oklahoma, west-central Texas, and east-central New Mexico (Willis 1967: 302); also recorded from +"Arizona" +(Erwin and Pearson 2008: 202). + + + +Records. + +USA +: KS, NM, OK, TX [AZ] + + + + \ No newline at end of file diff --git a/data/38/6E/51/386E51835DA6FBCB48069FD675D5DE1C.xml b/data/38/6E/51/386E51835DA6FBCB48069FD675D5DE1C.xml new file mode 100644 index 00000000000..0570c96c2a8 --- /dev/null +++ b/data/38/6E/51/386E51835DA6FBCB48069FD675D5DE1C.xml @@ -0,0 +1,88 @@ + + + +Records of Hedotettix and Teredorus in Thailand with the description of three new species (Orthoptera, Tetrigidae) + + + +Author + +Zha, Ling-Sheng + + + +Author + +Wen, Ting-Chi + + + +Author + +Kang, Ji-Chuan + + + +Author + +Hyde, Kevin D. + +text + + +ZooKeys + + +2016 + +556 + + +83 +95 + + + + +http://dx.doi.org/10.3897/zookeys.556.6002 + +journal article +http://dx.doi.org/10.3897/zookeys.556.6002 +1313-2970-556-83 +B03E1DFFB6DB413BB2710AC97DAE2796 +B03E1DFFB6DB413BB2710AC97DAE2796 + + + +Taxon classification Animalia Orthoptera Tetrigidae + + + +Hedotettix Bolivar, 1887 in Thailand + + + + +Key to species of +Hedotettix +Bolivar, 1887 in Thailand + + + + + + + + + +
+Hedotettix gracilis +(De Haan, 1843) +
+Hedotettix triangularis +sp. n. +
+
+
+
+
\ No newline at end of file diff --git a/data/38/6E/7A/386E7A96E8BA88354B4822230741E97E.xml b/data/38/6E/7A/386E7A96E8BA88354B4822230741E97E.xml new file mode 100644 index 00000000000..be08f7de129 --- /dev/null +++ b/data/38/6E/7A/386E7A96E8BA88354B4822230741E97E.xml @@ -0,0 +1,87 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part P) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +718 +782 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Plantago strictissima +Linnaeus + +, + +Amoenitates Academicae +4 + +: 478. 1759 + + +. + + + +"Habitat [Monspelii.]" + + +Type not designated. + + +Original material: none traced. + + + +Current name: + +Plantago maritime +L. + +( +Plantaginaceae +). + + + + +Note: +See discussion of this name by Stearn (in Geck & Pressler, +Festschr. Claus Nissen +: 640-641. 1974). + + + + \ No newline at end of file diff --git a/data/38/6E/87/386E87B3664C9C09FF5F578B010FF807.xml b/data/38/6E/87/386E87B3664C9C09FF5F578B010FF807.xml new file mode 100644 index 00000000000..5a88a78bd94 --- /dev/null +++ b/data/38/6E/87/386E87B3664C9C09FF5F578B010FF807.xml @@ -0,0 +1,136 @@ + + + +New genus and species of Hexagenitidae (Insecta: Ephemeroptera) from Yixian Formation, China + + + +Author + +Huang, Jiandong + + + +Author + +Ren, Dong + + + +Author + +Shih, Chungkun + +text + + +Zootaxa + + +2007 + +1629 + + +39 +50 + + + +journal article +10.5281/zenodo.179369 +f43b5459-3507-44de-ba79-433bad90c141 +1175-5326 +179369 + + + + + + + +Epicharmeropsis hexavenulosus +Huang, Ren & Shih + +, +sp. nov. + + + + +( +Fig. 1–4 +.) + + + + +Etymology. +Latin prefix +hexa- +(six) and +venulosus +(veinlet). + + + + + +Holotype +. + +CNU-E-YX-2007001-1, CNU-E-YX-2007001-2 ( +Fig. 1–3 +). Well preserved part and counterpart of imago; antennae and tarsi of middle and hind legs are not preserved; the Late Jurassic to the Early Cretaceous, Yixian Formation, Shimen Village, Yangshuling Township, Pingquan County, Hebei Province, +China +. + + +Material. +Holotype +and from the same locality, +paratypes +: male imago, No. CNU-E-YX-2007021-1, No. CNU-E-YX-2007021-2; male imago, No. CNU-E-YX-2007023; male imago, No. CNU-E-YX-2007024; male imago, No. CNU-E-YX-2007025-1, No. CNU-E-YX-2007025-2; female imago, No. CNU-E-YX- 2007004 ( +Fig. 4 +.). + + + + +Diagnosis. +In addition to the diagnosis for the new genus, the species can be diagnosed as follows: CuA1 of forewing with 6 triads (loop-shaped veinlets) leading to wing margin. + + + + +Description. +Male imago (dorsal view) ( +Fig. 1–3 +.). + +Eyes relatively large, contiguous. Pterothorax well-developed; mesonotal suture (MNs) in anterior part of mesonotum strongly stretched backwards medially, not transverse; paired medioparapsidal sutures (MPs) jointed at middle area of mesonotum, not parallel; metanotum long, with evident scutum. +Forewing: broad and triangular with costal brace; costal margin slightly curved; tornoapical (outer) margin longer than basitornal (anal) margin; costal area relatively wide, narrowing toward tip; RA subparallel to SC; membrane slightly thickened at distal part of the field between C and RA; RSa formed two triads, RSp non-branched; MA branched after middle area of wing; MA1 and MA2 uniformly diverging; iMA approximated MA2; MP1 and MP2 diverged at an angle of approximately 30 degree; distinct intercalary veins existing between MP2 and CuA1; CuA bifurcated to CuA1 and CuA2, from the bifurcation a vein iCu formed 6 triads following one another: anterior branch of each triad forms next triad; each of these triads has anterior branch arched by its convexity anteriorly; all branches of these triads go to basitornal margin of wing. + +Hind +wing: broad with fairly obtuse tip; venation relatively profuse; the base of C strongly arched, far from SC; subcostal area broad, more than 3 times as wide as costal area; RA terminated near wing apex; RS formed triad RSa-iRS-RSp, RSa and RSp non-branched; MA bifurcated near middle; MP bifurcated near the base of wing; iMP approximated with MP1; CuA and CuP un-forked; more than 4 A present; anal area broad; numerous crossveins and intercalary veins near wing margin. + +Legs (preserved): relatively sturdy and long; femora longer than tibia; three-segmented tarsi of fore legs preserved, slender; tarsi of middle and hind legs absent. +Abdomen: the posterolateral projections of the ninth segment, very long and sharp, nearly as long as the tenth abdominal tergum. +Paracercus, very short; cerci, long. + +Female imago ( +Fig. 4 +.). Eyes relatively small, separate; mouth apparatus vestigial, only anterior margin of the frons forming a projected lamella; coxa, trochanter and femur of fore and middle legs preserved, sturdy; the posterolateral projections of the ninth segment not extended posterolaterally. Other characters are as in male. + +Male and female subimagoes, and nymph are unknown. + +Measurements +(mm). +Holotype +: body length (excluding caudalii) 31.0 (head length 3.0, pronotum length 0.5, pterothorax length 9.5, abdomen length 18.0); forewing length 34.0, its width 14.0; hind wing length 18.0, its width 11.0; length of fore leg fragment 27.0 (femur 9.0, tibia 7.0, first tarsus 4.0, second tarsus 5.0, third preserved tarsus 2.0); femora of middle and hind legs 6.0; tarsi of middle and hind legs 5.0. +Paratype +: female imago No.CNU-E-YX-2007004, forewing length 34.0, its width 14.5. + + + + \ No newline at end of file diff --git a/data/38/6E/87/386E87B3664D9C03FF5F500206D7FEEE.xml b/data/38/6E/87/386E87B3664D9C03FF5F500206D7FEEE.xml new file mode 100644 index 00000000000..4e080f86be7 --- /dev/null +++ b/data/38/6E/87/386E87B3664D9C03FF5F500206D7FEEE.xml @@ -0,0 +1,190 @@ + + + +New genus and species of Hexagenitidae (Insecta: Ephemeroptera) from Yixian Formation, China + + + +Author + +Huang, Jiandong + + + +Author + +Ren, Dong + + + +Author + +Shih, Chungkun + +text + + +Zootaxa + + +2007 + +1629 + + +39 +50 + + + +journal article +10.5281/zenodo.179369 +f43b5459-3507-44de-ba79-433bad90c141 +1175-5326 +179369 + + + + + + + +Epicharmeropsis quadrivenulosus +Huang, Sinitshenkova & Ren + +, +sp. nov. + + + + +( +Fig. 5–7 +.) + + + + +Etymology. +Latin prefix +quadri- +(four) and +venulosus +(veinlet) + + + + + +Holotype +. + +Male imago, No. CNU-E-YX-2007002 ( +Fig. 5–6 +.). Well preserved fore and hind wings as well as head and thorax, other parts of the specimen not preserved, the Late Jurassic to the Early Cretaceous, Yixian Formation, Jianshangou, Chaomidian Village, Shangyuan Township, Beipiao City, Liaoning Province, +China +. + + + +Paratype +. + +Male imago, No.CNU-E-YX-2007014 ( +Fig. 7 +.) from Yixian Formation (the Late Jurassic to the Early Cretaceous), Dakangpu Village, Liulongtai Township, Yixian County, Liaoning Province; male imago, No.CNU-E-YX-2007020 from Yixian Formation, Shimen Village, Yangshuling Township, Pingquan County, Hebei Province; male imago, No.CNU-E-YX-2007007 from Yixian Formation, Jianshangou, Chaomidian Village, Shangyuan Township, Beipiao City, Liaoning Province; male imago, No. CNU-E-YX- 2007008 from Yixian Formation, Huangbanjigou, Chaomidian Village, Shangyuan Township, Beipiao City, Liaoning Province, +China +. + + + + +Diagnosis. +In addition to the diagnosis for the new genus, the species can be diagnosed as follows: CuA1 of forewing with 4 triads (loop-shaped veinlets) leading to wing margin. + + + + +Description. +Male imago ( +Fig. 5–7 +.). CuA1 of fore wing with 4 loop-shaped veinlets leading to wing margin; left hind wing is not completely same with right hind wing, RSa of left hind wing branched and iRSa absent, however, RSa of right hind wing unforked and iRSa present. Other characters are similar to those of male + +E. hexavenulosus + +. + +Female imago, male and female subimagoes, and nymph are unknown. + + +FIGURE 2. + +Epicharmeropsis hexavenulosu + +s gen. et +sp. nov. +, male imago, holotype CNU-E-YX-200701-1: A, photograph of head and thorax in dorsal view; B, photograph of cubital area on forewing. Without scale. + + + + +FIGURE 3. + +Epicharmeropsis hexavenulosu + +s +sp. nov. +, male imago, holotype: A, body with wings, CNU-E-YX-200701- 1; B, forewing, CNU-E-YX-200701-2.; C, hind wing, CNU-E-YX-200701-2. MNs – mesonotal suture, MPs - medioparapsidal suture, LPs – lateroparapsidal suture. + + + + +FIGURE 4. + +Epicharmeropsis hexavenulosu + +s +sp. nov. +, female imago, paratype CNU-E-YX-2007004: A, photograph of paratype; B, body with wings on lateral view; C, forewing. + + + +Comparison. + +E. quadrivenulosus + + +sp. nov. + +can be distinguished from + +E. hexavenulosus + + +sp. nov. + +by 4 triads (loop-shaped veinlets). + + + +FIGURE 5. + +Epicharmeropsis quadrivenulosus + + +sp. nov. + +, male imago, holotype CNU-E-YX-2007002: A, photograph of part; B, forewing; C, left hind wing. + + + +Measurements +(mm). +Holotype +: forewing length 38.5, its width 15.5; hindwing length 21.0, its width 13.0; pronotum length 1.0; mesonotum 10.0. +Paratype +: male imago No.CNU-E-YX-2007014, body length 30.0 (excluding caudalii), forewing length 32.0, its width 13.0; male imago No.CNU-E-YX-2007011-1, forewing length 37.0, its width 15.5, hindwing length 17.0, its width 13.0. + + + + \ No newline at end of file diff --git a/data/38/6E/87/386E87B3664F9C0AFF5F545B007CF829.xml b/data/38/6E/87/386E87B3664F9C0AFF5F545B007CF829.xml new file mode 100644 index 00000000000..9a3c3893a42 --- /dev/null +++ b/data/38/6E/87/386E87B3664F9C0AFF5F545B007CF829.xml @@ -0,0 +1,166 @@ + + + +New genus and species of Hexagenitidae (Insecta: Ephemeroptera) from Yixian Formation, China + + + +Author + +Huang, Jiandong + + + +Author + +Ren, Dong + + + +Author + +Shih, Chungkun + +text + + +Zootaxa + + +2007 + +1629 + + +39 +50 + + + +journal article +10.5281/zenodo.179369 +f43b5459-3507-44de-ba79-433bad90c141 +1175-5326 +179369 + + + + + + +Genus + +Epicharmeropsis +Huang, Ren & Shih + +, gen. nov. + + + + + + + +Type +species. + + +Epicharmeropsis hexavenulosus +Huang, Ren & Shih + +, + +sp. nov. + + + + + +Etymology. +Greek prefix +Epichar- +(beautiful) and +meropsis +(a suffix taken from genus + +Ephemeropsis + +). + + + + +Diagnosis. +Imago. Moderate to good-sized species; mesonotal suture (MNs) in anterior part of mesonotum strongly stretched backwards medially, not transverse; paired medioparapsidal sutures (MPs) anastomosed at middle area of mesonotum, not parallel; lateroparapsidal suture (LPs) curved laterally; metanotum relatively long. Forewing about 2.4 times as long as its width; membrane thickened at distal part of the field between C and RA; RS forking about +10mm +from base of forewing, RSa formed two triads, RSp nonbranched; distinct intercalary veins existing between MP2 and CuA1; CuA1 with 4–6 triads (loop-shaped veinlets) leading to wing margin; numerous crossveins and intercalary veins between longitudinal veins. Hindwing more or less than half as long as forewing, broad, about 1.6 times as long as its width with fairly obtuse tip. + + +Composition. +The +type +species and + +Epicharmeropsis quadrivenulosus + +. + + + + +Comparison. + +Epicharmeropsis + + +gen. nov. + +is very similar to + +Ephemeropsis +Eichwald + +from the Early Cretaceous of Transbaikalia and +Mongolia +in the shape and venation of fore and hind wings; but it differs from + +Ephemeropsis + +by membrane thickened at distal part of the field between C and RA, unforked RSp, and the distinct intercalary veins existing between MP2 and CuA1 of forewing. The later two features of wing venation are present in Late Jurassic genus + +Hexagenites +Scudder, 1880 + +and Lower Cretaceous genus + +Cratogenites +Martins-Neto, 1996 + +, but in contrast to them, hind wing of + +Epicharmeropsis + +is more or less than half as long as forewing. + + + + +Remark. +The combined characters of this new genus allow an allocation of it to the family +Hexagenitidae +: moderate to large size; vein CuA of forewing forked, one of its branches with a series of triads (loopshaped veinlets) leading to wing margin. + + + +Epicharmeropsis + + +gen. nov. + +possesses a peculiar combination of characters: mesonotal suture (MNs) in anterior part of mesonotum strongly stretched backwards medially, not transverse; paired medioparapsidal sutures (MPs) jointed at middle area of mesonotum, not parallel; forewing less than 2.5 times as long as its width; RSp non-branched; the presence of intercalary veins between MP2 and CuA1; hindwing broad, about 1.6 time as long as its width, with fairly obtuse tip. These characters allow formal separation of this new genus from other known genera of the +Hexagenitidae +established by mayfly adults, extant or in fossil records. + + + + \ No newline at end of file diff --git a/data/38/6F/D3/386FD350FFECCA12FF2B4C1F8E6BE733.xml b/data/38/6F/D3/386FD350FFECCA12FF2B4C1F8E6BE733.xml new file mode 100644 index 00000000000..71942ae7b53 --- /dev/null +++ b/data/38/6F/D3/386FD350FFECCA12FF2B4C1F8E6BE733.xml @@ -0,0 +1,90 @@ + + + +Morphology and life cycle of Carybdea morandinii, sp. nov. (Cnidaria), a cubozoan with zooxanthellae and peculiar polyp anatomy + + + +Author + +Straehler-Pohl, Ilka + + + +Author + +Jarms, Gerhard + +text + + +Zootaxa + + +2011 + +2755 + + +36 +56 + + + +journal article +10.5281/zenodo.203576 +f6dd2934-77ab-47b2-8774-580ee2a0c8f6 +1175-5326 +203576 + + + + + + + +Carybdea morandinii + +, +sp. nov. + + + + + + +Holotype +— one preserved cubopolyp, from a culture established from specimens obtained in a saltwater tank at Hagenbecks Tierpark, Hamburg, +Germany +, and originally from +east Asia +, deposited in collections of the Zoologisches Institut und Zoologisches Museum, Universität Hamburg ( +ZMH +) No.C.11999. + + +Paratype +series —20 preserved, fully developed cubopolyps with buds, 10 preserved cubopolyps without buds, one young medusa, and five preserved creeping cubopolyps, +ZMH +No.C.11750. + + +Type +locality — On coral rock, originally from +east Asia +, in a seawater tank at Hagenbecks Tierpark (Zoo), Hamburg, +Germany +. + +Additional material – living polyps under cultivation in our laboratory. + +Etymology — The specific name “ + +morandinii + +” honours Dr. André Carrara Morandini, a well known Medusozoa morphologist and taxonomist. Dr. Morandini was working as a guest researcher in our laboratory when the species was discovered. His knowledge of Cubozoa helped determine that the cubopolyps likely represented a new species. + +Diagnosis + + + \ No newline at end of file diff --git a/data/38/70/2A/38702ABBEF81209793160B594D0353F3.xml b/data/38/70/2A/38702ABBEF81209793160B594D0353F3.xml new file mode 100644 index 00000000000..4dd171dd5b7 --- /dev/null +++ b/data/38/70/2A/38702ABBEF81209793160B594D0353F3.xml @@ -0,0 +1,72 @@ + + + +Order Carnivora + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +532 +628 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Acinonyx jubatus +subsp. +soemmeringii +Fitzinger 1855 + + + + + +Synonyms: + +Acinonyx jubatus +subsp. +megabalica +(Heuglin 1863) + +; + +Acinonyx jubatus +subsp. +wagneri +Hilzheimer 1913 + +. + + + + \ No newline at end of file diff --git a/data/38/70/C3/3870C3195A1A5997AA430033807720C7.xml b/data/38/70/C3/3870C3195A1A5997AA430033807720C7.xml new file mode 100644 index 00000000000..222979da5ac --- /dev/null +++ b/data/38/70/C3/3870C3195A1A5997AA430033807720C7.xml @@ -0,0 +1,142 @@ + + + +New records of water mites (Acari, Hydrachnidia) from Portugal revealed by DNA barcoding, with the description of Atractides marizae sp. nov. + + + +Author + +Pesic, Vladimir +https://orcid.org/0000-0002-9724-345X +Department of Biology, University of Montenegro, Cetinjski put b. b., 81000 Podgorica, Montenegro +vladopesic@gmail.com + + + +Author + +Jovanovic, Milica +Department of Biology, University of Montenegro, Cetinjski put b. b., 81000 Podgorica, Montenegro + + + +Author + +Espiridiao Oliveira, Amalia +Mediterranean Institute for Agriculture, Environment and Development (MED), CHANGE - Global Change and Sustainability Institute, Institute for Advanced Studies and Research, Universidade de Evora, Polo da Mitra, Ap. 94, 7006 - 554, Evora, Portugal + + + +Author + +Pedro, Ana +Mediterranean Institute for Agriculture, Environment and Development (MED), CHANGE - Global Change and Sustainability Institute, Institute for Advanced Studies and Research, Universidade de Evora, Polo da Mitra, Ap. 94, 7006 - 554, Evora, Portugal + + + +Author + +Freira, Marvin +Mediterranean Institute for Agriculture, Environment and Development (MED), CHANGE - Global Change and Sustainability Institute, Institute for Advanced Studies and Research, Universidade de Evora, Polo da Mitra, Ap. 94, 7006 - 554, Evora, Portugal + + + +Author + +Morais, Maria Manuela +https://orcid.org/0000-0003-0482-4309 +Mediterranean Institute for Agriculture, Environment and Development (MED), CHANGE - Global Change and Sustainability Institute, Institute for Advanced Studies and Research, Universidade de Evora, Polo da Mitra, Ap. 94, 7006 - 554, Evora, Portugal & Water Laboratory, University of Evora, P. I. T. E. Rua da Barba Rala No. 1, 7005 - 345 Evora, Portugal + +text + + +ZooKeys + + +2023 + +2023-03-01 + + +1151 + + +205 +222 + + + + +http://dx.doi.org/10.3897/zookeys.1151.100766 + +journal article +http://dx.doi.org/10.3897/zookeys.1151.100766 +1313-2970-1151-205 +6F3BA97A4EB447B48ADD4375417D9C78 +BC921697FEFE525D83E85520EBA1E2B3 + + + + +Lebertia pusilla Koenike, 1911 + + + +Material examined. + + +Portugal +, + +Santarem + +, +Caniceira +stream, +39.4110°N +, +8.2615°W +, +25.v.2022 +, leg. + +Jovanovic + +, +2♂ +, +4♀ +, +2♀ +sequenced (Table +1 +) + +. + + + +Remarks. + +The Portuguese specimens molecularly analyzed in this study match the description of + +L. pusilla + +, a species widely distributed in the Palaearctic ( +Di Sabatino et al. 2010 +). They share the presence of only one short swimming seta on II-L-5 and two or three swimming setae on anterior IV-L-5. It is likely that the lineage from Portugal represents a cryptic species, with a +p +-distance of 9.39-9.79% to the nearest sequence (NLACA493-15) of + +L. pusilla + +from the Netherlands. + + + +Distribution. +Europe. + + + \ No newline at end of file diff --git a/data/38/71/35/387135A71C62DD19D6C39CF0C66DDC8B.xml b/data/38/71/35/387135A71C62DD19D6C39CF0C66DDC8B.xml new file mode 100644 index 00000000000..9883cbf3f68 --- /dev/null +++ b/data/38/71/35/387135A71C62DD19D6C39CF0C66DDC8B.xml @@ -0,0 +1,167 @@ + + + +Flora der Schweiz und angrenzender Gebiete. Band 2. Nymphaceae bis Primulaceae (2 nd edition) (p. 956): Primulaceae + + + +Author + +Hess, Hans Ernst + + + +Author + +Landolt, Elias + + + +Author + +Hirzel, Rosmarie + +text + +1976 +Birkhaeuser Verlag + + +https://doi.org/10.5281/zenodo.292251 + +book +292251 +10.5281/zenodo.292251 +3-7643-0527-4 + + + +<subSubSection id="4D8225B48A68181C68A4A1373537BCF9" pageId="null" pageNumber="929" type="nomenclature"> +<paragraph id="3352DEF6D0DB3E1E02A8D4AD8823D964" pageId="null" pageNumber="929"> +<taxonomicName id="5A7CD6CD217BF9055428C8F98F6BEB2A" authority="L." class="Magnoliopsida" family="Primulaceae" genus="Primula" kingdom="Plantae" order="Ericales" pageId="null" pageNumber="929" phylum="Tracheophyta" rank="species" species="minima"> +<pageBreakToken id="4B1E397997D6098E0CE8FDB087818E5B" pageId="null" pageNumber="929">Primula</pageBreakToken> +<normalizedToken id="7A458F3EE6039D2A7397082E7063DE77" originalValue="mínima" pageId="null" pageNumber="929">minima</normalizedToken> +<authorityName id="E6D0A3426B95CE10A84669AADD15693A" pageId="null" pageNumber="929">L.</authorityName> +</taxonomicName> +</paragraph> +</subSubSection> +<subSubSection id="651BB411F443E4A1E49037E40C042451" pageId="null" pageNumber="929" type="vernacular_names"> +<paragraph id="1928052A1F05C56649D683DF5ABC124F" pageId="null" pageNumber="929"> +<normalizedToken id="2A1BB33B0B9A6AFECCF49870586FBB6D" originalValue="Zwerg-Schlüsselblume" pageId="null" pageNumber="929">Zwerg-Schluesselblume</normalizedToken> +</paragraph> +</subSubSection> + + + + +Blaetter +bis 1,5 cm lang + +und 0,8 cm breit, +allmaehlich +gegen den Grund +verschmaelert +(fast kein Stiel), +gestutzt +, beiderseits +hellgruen +und scheinbar kahl (besonders am Rand kaum 0,05 mm lange, farblose +Druesenhaare +vorhanden), ohne Mehlstaub, + +am vorderen Rand mit scharf zugespitzten +Zaehnen + +, in der Knospenlage gegen die Oberseite eingerollt. Stengel 0,2-1,5 cm hoch, kahl, ohne Mehlstaub, + +1-, selten 2 +bluetig +. + +Tragblaetter +, +Bluetenstiele +und Kelch scheinbar kahl (ganz kurze +Druesenhaare +vorhanden). +Tragblaetter +3-7 mm lang und +1/4-1/2 +so breit. +Bluetenstiel +undeutlich. Kelch 5-8 mm lang, +1/2-3/4 +so lang wie die +Kronroehre +, unterhalb der +Zaehne +2,5-4 mm im Durchmesser; +Kelchzaehne +2-3 mm lang, +mit aufgesetzter Spitze +, +11/2 +-2mal so lang wie breit. Krone rot, am Schlundeingang +weiss +, ohne Mehlstaub, mit bis 0,5 mm langen +Druesenhaaren +, kaum duftend, mit weit +trichterfoermig +ausgebreiteten, 7-12 mm langen, ziemlich tief ausgerandeten Kronzipfeln; +Kronroehre +aussen +kahl. Frucht 3-5 mm lang und fast so dick, etwa +1/2 +so lang wie der Kelch. - +Bluete +: +Frueher +Sommer. + + +Zytologische Angaben. 2n ca. 64: +Ohne Herkunftsangabe des Materials (Bruun 1932b). +2n += +66, 67, 68, 69, 70, 73: +Material aus Innsbruck; an Material aus den Dolomiten wurde nur 2n = 67 +gezaehlt +(Kress 1963). + + +Standort. +Alpin, selten subalpin. Humose, feinerdereiche, kalkarme +Boeden +. Gipfelrasen, +Schneetaelchen +, Ruhschutt, Felsspalten. +Caricetum curvulae +(Kerner) Brockmann-Jerosch 1907. + + + +Verbreitung. Mittel- und +suedeuropaeische +Gebirgspflanze + +( + +oestlich + +) +: +Ostalpen ( +westwaerts +bis Bayern, Brenner, Tonale), Sudeten, Karpaten, Serbien, Bulgarische Gebirge. Verbreitungskarte von +Luedi +in Hegi V/3 (1927). - Im Gebiet: +Nordoestliche +Bergamasker Alpen (Monte Gavio, Monte Tozzo, Monte Tonale; zweifelhafte Angaben von der +Suedseite +des Umbrail und von Zana im Val Malenco), Vintschgau (von Meran +ostwaerts +). + + + + \ No newline at end of file diff --git a/data/38/71/37/3871371714158476095392F43019ABF8.xml b/data/38/71/37/3871371714158476095392F43019ABF8.xml new file mode 100644 index 00000000000..24d2ecfcec4 --- /dev/null +++ b/data/38/71/37/3871371714158476095392F43019ABF8.xml @@ -0,0 +1,85 @@ + + + +Guide to the Vascular Flora of the Savannas and Flatwoods of Shaken Creek Preserve and Vicinity (Pender & Onslow Counties, North Carolina, U. S. A.) + + + +Author + +Thornhill, Robert + + + +Author + +Krings, Alexander + + + +Author + +Lindbo, David + + + +Author + +Stucky, Jon + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1099 +1099 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1099 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1099 +1314-2828--1099 + + + + +Trillium pusillum var. pusillum Michx. + + + +Ecological interactions + +Conservation status +State E, FSC; S2, G3T2. + + + +Distribution +Margins of pine savannas and adjacent swamps. + + +Notes + +Late +Mar-May +; +Jun-Jul +. Reported from Sandy Run by +LeBlond and Weakley (1991) +, but no specimens have been seen in Shaken Creek Preserve by the senior author. [< +Trillium pusillum +Michx. sensu RAB; <FNA; = Weakley] + + + + \ No newline at end of file diff --git a/data/38/71/F1/3871F170AB3E6364E54D8BE49DB690AC.xml b/data/38/71/F1/3871F170AB3E6364E54D8BE49DB690AC.xml new file mode 100644 index 00000000000..ef8bad67952 --- /dev/null +++ b/data/38/71/F1/3871F170AB3E6364E54D8BE49DB690AC.xml @@ -0,0 +1,196 @@ + + + +Three new species of the genus Zodarion (Araneae, Zodariidae) from China + + + +Author + +Zhang, Bao-Shi + + + +Author + +Zhang, Feng + +text + + +ZooKeys + + +2019 + +813 + + +67 +87 + + + + +http://dx.doi.org/10.3897/zookeys.813.29683 + +journal article +http://dx.doi.org/10.3897/zookeys.813.29683 +1313-2970-813-67 +75FB5405582940128148EDA92ED5E082 +75FB5405582940128148EDA92ED5E082 + + + + +Zodarion planum +sp. n. +Figures 4, 5 + + + + +Type +material. + + +Holotype ♂ (Z-Shaanxi-198606-22), Baoji City ( +34°22'N +, +107°09'E +), Shaanxi Province, China, 22 June 1986, Mingsheng Zhu leg. + + + +Diagnosis. + +The male of +Z. planum +is very similar to those of +Z. sytchevskajae +Nenilin & Fet, 1985, +Z. chaoyangense +Zhu & Zhu, 1983, and +Z. furcum +Zhu, 1988, as all have dorsolateral processes extending from the middle part of the retrolateral tibial apophysis, though +Z. planum +can be distinguished from the others by the wide and fluent margins of the dorsolateral process (obviously curving in the other three species) (Figs 4 +C-E +, 5 +A-C +). + + + +Figure 4. +Zodarion planum +sp. n., male holotype ( +A-E +) A, B Habitus (A dorsal view B ventral view) +C-E +Left male palp (C prolateral view D ventral view E retrolateral view). + + + + +Figure 5. +Zodarion planum +sp. n. +A-C +Left male palp of male holotype (A prolateral view B ventral view C retrolateral view). Abbreviations: C, conductor; DLH, dorsolateral hook; E, embolus; RTA, retrolateral tibial apophysis; TA, tegular apophysis; TAH, tegular apophysis hook; TU, tutaculum. + + + + + +Etymology +. + +The specific name is from the Latin planum, in reference to the dorsolateral hook-shaped process of the retrolateral tibial apophysis; adjective. + + +Description. + +Male (holotype): total length 2.22; carapace 1.20 long, 1.00 wide; opisthosoma 1.02 long, 0.74 wide. Carapace (Fig. 4A) declining, longer than wide, yellow-brown, furnished with inconspicuous black netlike stripes. Clypeus 0.16 high, yellow-brown. Anterior eye row slightly procurved, posterior eye row strongly procurved in dorsal view. Ocular area black. Eye sizes and interdistances: AME 0.13, ALE 0.08, PME 0.07, PLE 0.07, +AME-AME +0.04, +AME-ALE +0.06, +ALE-ALE +0.42, +AME-PME +0.08, +PME-PME +0.16, +PME-PLE +0.02, +PLE-PLE +0.42, +ALE-PLE +0.02. MOQ 0.26 long, anterior width 0.28, posterior width 0.29. Mouthparts (Fig. 4B): chelicerae yellow-brown, with two anterior and one posterior teeth on margins of fang furrows, terminal part with row of black scopulae, fangs short; endites yellowish, apices paler and provided with dense black scopula; labium triangular, 0.16 long, 0.25 wide, yellow-brown. Sternum (Fig. 4B) 0.70 long, 0.64 wide, white, lateral margin dark, provided with sparse black setae, its lateral margin with inter- and intra-coxal triangles. Legs (Fig. 4A, B) yellow-brown; femora with dorsal spines. Leg measurements: leg I 5.32 (0.98 + 0.51 + 1.47 + 1.66 + 0.70), II 2.78 (0.78 + 0.38 + 0.65 + 0.59 + 0.38), III 4.41 (0.92 + 0.38 + 1.54 + 1.00 + 0.57), IV 5.79 (1.12+ 0.58 + 1.31 + 1.70 + 1.08). Opisthosoma (Fig. 4A, B) covered with black short setae. Dorsum of opisthosoma black; venter white, median part with wide dark gray band. Spinnerets (Fig. 4B) white, laterally with blackish patches. + + +Palp (Figs 4C, D, 5 +A-C +). Coxae of palps white, other sections yellow; length to width ratio of femur 2.7, length to width ratio of patella 1.2; retrolateral tibial apophysis about 2.5 times the tibial length, thin apex finger-shaped, dorsolateral hook-shaped apophysis long and flat; cymbium with terminal spine, tutaculum obvious; tegular apophysis of moderate size, retrolaterally with flat and wide extension, tegular apophysis hook nearly straight in prolateral view; membranous conductor long, lamellate, and running almost along whole course of embolus; basal embolus almost triangular. + +Female unknown. + + +Distribution. +China (Shaanxi). + + +Remarks. + +The two new species +Z. apertum +sp. n. and +Z. planum +sp. n., together with most known East Asian and Central Asian species of the +Zodarion +(i.e. +Z. asiaticum +Tyschchenko, 1970, +Z. bekuzini +Nenilin, 1985, +Z. chaoyangense +Zhu & Zhu, 1983, +Z. continentale +Andreeva & Tyschchenko, 1968, +Z. furcum +Zhu, 1988, +Z. mongolicum +(Marusik & Koponen, 2001), +Z. nenilini +Eskov, 1995 (also distributed in European area and Urals of Russia), +Z. proszynskii +Nenilin & Fet, 1985, +Z. schmidti +(Marusik & Koponen, 2001), +Z. spasskyi +Charitonov, 1946, +Z. hunanense +Yin, 2012, +Z. sytchevskajae +Nenilin & Fet, 1985, +Z. volgouralensis +(Ponomarev, 2007) (also distributed in Astrakhan of Russia), and +Z. zebra +Charitonov, 1946) appear to comprise an undescribed group with the following common characters: the long and thin embolus rising at the prolateral or basal part of the tegulum; tegular apophysis wide and strong, with a downwardly-directed hook; a modified apical portion of the retrolateral tibial +apophysis +turning dorsally; cymbium with tutaculum; epigyne with incised posteromedian margin and median hood; apical parts of spiraled spermathecae converging. They are different from the lutipes group ( +Bosmans 2009 +) in having a long conductor, the tutaculum of the cymbium, and the converging apex of the spermathecae. + + +Zodarion hunanense +was described based only on a female specimen from Hunan province of China. The possibility exists that +Z. planum +sp. n. is conspecific with +Z. hunanense +. + + + + \ No newline at end of file diff --git a/data/38/71/F2/3871F243B7A37E11F48F075D6B455E82.xml b/data/38/71/F2/3871F243B7A37E11F48F075D6B455E82.xml new file mode 100644 index 00000000000..b8cf393b02c --- /dev/null +++ b/data/38/71/F2/3871F243B7A37E11F48F075D6B455E82.xml @@ -0,0 +1,413 @@ + + + +Info Flora Schweiz - Poaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/poaceae.html + +url + + + + + +Miscanthus sinensis +Andersson + + + + + +Chinaschilf + + + + +Art ISFS: 262250 Checklist: 1029320 +Poaceae +Miscanthus +Miscanthus sinensis Andersson + + + +Bestimmungsschluessel + + + +Zusammenfassung + + + + +Artbeschreibung + +(nach +Lauber & al. 2018 +) + +: +1-2,5 m hoch, dichte Horste bildend +. +Blaetter +oben +gehaeuft +, steif, +1-3 cm +breit und +40-80 cm +lang. + +Bluetenstand +faecherfoermig + +mit zahlreichen schmalen, +15-30 cm +langen Trauben. +Aehrchen +paarig, +4-7 mm +lang, am Grund +7-12 mm +lang behaart, 2 +bluetig +. Obere +Bluete +zwittrig, untere +maennlich +. Deckspelzen der oberen +Bluete +mit + +8-15 mm +langer Granne + +. Der Hybride + +M. sinensis + +x + +sacchariflorus + +( +M. +x +giganteus +, +2-4 m +hoch, +Blaetter +3-4 cm +breit, +Blueten +grannenlos) wird als Energiepflanze kultiviert. + + + + +Bluetezeit + +(nach +Lauber & al. 2018 +) + +: 8-10 + + +Standort und Verbreitung in der Schweiz + +(nach +Lauber & al. 2018 +) + +: Als Zierpflanze in vielen Formen kultiviert und selten auf +Ruderalflaechen +und Brachen verwildert / kollin / + + + + +Verbreitung global + +(nach +Lauber & al. 2018 +) + +: Stammt aus Ostasien + + + + +Oekologische +Zeigerwerte + +(nach +Landolt & al. 2010 +) + +334-44 + 4.h.2n=36-42 + + + + + +Oekologie + + + +Lebensform +Mehrjaehriger +Hemikryptophyt + + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + + + + + +
KEINE ANGABE
+
+
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +maessig +feucht +Lichtzahl LhellSalzzeichen--
Reaktionszahl Rschwach sauer bis neutral (pH 4.5-7.5)Temperaturzahl Twarm-kollin
+Naehrstoffzahl +N + +naehrstoffreich + +Kontinentalitaetszahl +K +subkontinental (niedrige relative Luftfeuchtigkeit, grosse Temperaturschwankungen, eher kalte Winter)
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Miscanthus sinensis +Andersson + + + + + + +Volksname Deutscher Name: +Chinaschilf +Nom +francais +: +Roseau de Chine +, +Eulalie +Nome italiano: + +Eulalia +sinese + + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Miscanthus sinensis Andersson + + +Checklist 2017 + +262250
= +Miscanthus sinensis Andersson + + +Flora Helvetica 2001 + +2713a
= +Miscanthus sinensis Andersson + + +Flora Helvetica 2012 + +2891
= +Miscanthus sinensis Andersson + + +Flora Helvetica 2018 + +2891
= +Miscanthus sinensis Andersson + + +SISF/ISFS 2 + +262250
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Kommentare aus der +Checklist 2017 +Aus Kultur (Ziergras) verwildert. Ist eine der Elternpflanzen der als Energiepflanze angebauten +M +. +x +giganteus +. Checklist + + + + +Status Indigenat +: Kultivierter Neophyt: nach dem Jahr +1500 in +der Schweiz aufgetreten + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein +Art der "Liste der potenziell invasiven gebietsfremden Arten" + + +
+
\ No newline at end of file diff --git a/data/38/72/87/387287FCC301FFD7FF0DE265E495FD3B.xml b/data/38/72/87/387287FCC301FFD7FF0DE265E495FD3B.xml new file mode 100644 index 00000000000..68f61ee44b1 --- /dev/null +++ b/data/38/72/87/387287FCC301FFD7FF0DE265E495FD3B.xml @@ -0,0 +1,269 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + + +Merica succineiformis +( +Boettger, 1906 +) + +nov. comb. + + + + + + +Figs 7A +1–A +3 + + + + + + + +Cancellaria +( +Aphera +) +succineiformis +Boettger 1906: 51 + + +. + + + + + +Cancellaria +( +Aphera +) +succineiformis +Boettger + +— + +Zilch 1934: 260 + +, pl. 17, figs 24a–b. + +Type +material. + +SMF +Frankfurt +( +Germany +). + + + + + +FIGURE 7. A1–A3. + +Merica succineiformis +( +Boettger, 1906 +) + +, Coşteiu de Sus (Romania), SMF XII 2264 a, holotype. +B1–B3. + +Ovilia breitenbergerorum + +nov. sp. +, holotype, Mörtersdorf (Austria), NHMW 2012/0012/0001. +C1–C3. + +Ovilia excassidea +( +Sacco, 1894 +) + +, Gainfarn (Austria), NHMW 1846/0037/0288, holotype. +D1–D3. + +Ovilia tauroaspira +( +Sacco, 1894 +) + +, Mörtersdorf (Austria). +E1–E2. + +Ovilia + +? sp., Mörtersdorf (Austria). +F1–F3. + +Perplicaria mioquadrata +( +Sacco, 1894 +) + +, Lăpugiu de Sus (Romania), NHMW 2009z0098/0002, lectotype. +G1–G3. + +Perplicaria mioquadrata +( +Sacco, 1894 +) + +, Coşteiu de Sus (Romania), NHMW 2009z0098/0003. +H1–H3. + +Petitina inermis +(Pusch, 1837) + +, Enzesfeld (Austria), NHMW 2009z0098/0012. +I1–I2. + +Petitina inermis +(Pusch, 1837) + +, Enzesfeld (Austria), NHMW 2009z0098/0011. +J1–J3. + +Petitina inermis +(Pusch, 1837) + +, Grund (Austria), NHMW 1855/0045/0733. + + + + +Illustrated material. + +Figs 7A +1–A +3 +: specimen illustrated in +Zilch (1934 +, pl. 17, figs 24a–b), + +CoŞteiu +de Sus + +( +Romania +), height: +6 mm +, width: +3.7 mm +, +SMF + +XII 2264 + +a, +holotype +by monotypy + +. + + + + +Discussion. +A very rare species, which is known from a single specimen. It has a very low protoconch and a low and strongly convex early spire whorl. Based on its widely excavated columella and the shape of the columellar folds we place this species in + +Merica + +. Later whorls display an allometric growth resulting in a very wide and inflated last whorl, which resembles species of the cold water genus + +Nothoadmete +Oliver, 1982 + +. These species, however, lack the deeply concave columella and the fasciole as developed by + +Merica succineiformis + +. +Boettger (1906) +discussed a relation with + +Aphera +H. Adams & A. Adams, 1854 + +. The recent +type +species + +Aphera tessellata +( +Sowerby, 1832 +) + +has prominent columellar folds, a straight columella, is slender, ovoid and develops a characteristic sculpture of densely spaced beads. Therefore, a close relation of the Miocene species with + +Aphera + +is unlikely. The aperture is comparable with that of species of + +Bonellitia +Jousseaume, 1887b + +but the smooth shell and the expanding last whorl are atypical for this genus. + + + + +Distribution. +Only known so far from the early Badenian of the Paratethys. + + +Paratethys +—Badenian: Transylvanian Basin ( +Romania +: CoŞteiu de Sus). + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC303FFD7FF0DE786E3FFFCCA.xml b/data/38/72/87/387287FCC303FFD7FF0DE786E3FFFCCA.xml new file mode 100644 index 00000000000..b691a400393 --- /dev/null +++ b/data/38/72/87/387287FCC303FFD7FF0DE786E3FFFCCA.xml @@ -0,0 +1,76 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Ovilia +Jousseaume, 1887b + + + + + + + + + +Type +species: + +by original designation, + +Cancellaria doliolaris +Basterot, 1825 + +. +Early Miocene +, +France + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC306FFD2FF0DE150E795FB35.xml b/data/38/72/87/387287FCC306FFD2FF0DE150E795FB35.xml new file mode 100644 index 00000000000..7adcab3e072 --- /dev/null +++ b/data/38/72/87/387287FCC306FFD2FF0DE150E795FB35.xml @@ -0,0 +1,73 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Merica + +H. & A. Adams, 1854 + + + + + + + +Type +species: + +by subsequent designation of +Cossmann (1899) +, + +Cancellaria melanostoma +G. B. Sowerby +II, 1849 + +. Recent, Red Sea. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC307FFD3FF0DE168E239FBFC.xml b/data/38/72/87/387287FCC307FFD3FF0DE168E239FBFC.xml new file mode 100644 index 00000000000..83937ef4936 --- /dev/null +++ b/data/38/72/87/387287FCC307FFD3FF0DE168E239FBFC.xml @@ -0,0 +1,76 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Gulia +Jousseaume, 1887b + + + + + + + + +Type +species: + +by subsequent designation of +Cossmann (1888) +, + +Gulia acutangula +( +Faujas, 1817 +) + +, Early Miocene, +France +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC309FFDDFF0DE762E3EBFDE6.xml b/data/38/72/87/387287FCC309FFDDFF0DE762E3EBFDE6.xml new file mode 100644 index 00000000000..0eeae497712 --- /dev/null +++ b/data/38/72/87/387287FCC309FFDDFF0DE762E3EBFDE6.xml @@ -0,0 +1,76 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Contortia +Sacco, 1894 + + + + + + + + + +Type +species: + +by original designation, + +Cancellaria contorta +Basterot, 1825 + +. +Early Miocene +, +France + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC309FFDFFF0DE7C6E473FE5C.xml b/data/38/72/87/387287FCC309FFDFFF0DE7C6E473FE5C.xml new file mode 100644 index 00000000000..c87b97ac358 --- /dev/null +++ b/data/38/72/87/387287FCC309FFDFFF0DE7C6E473FE5C.xml @@ -0,0 +1,521 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + + +Contortia callosa +(Hörnes, 1854) + +nov. comb. + + + + + + +Figs 3J +, +5E +1–E +3 +, +5F +1–F +3 +, +5G +1–G +3 + + + + + + +Cancellaria callosa +Partsch + +— + +Hörnes 1848: 19 + +(nomen nudum). + + + + +Cancellaria callosa +Partsch + +—Hörnes 1854: 314, pl. 34, figs. 14–16 [ex Partsch MS.]. + + + + +Cancellaria callosa +Partsch + +— + +Hoernes & Auinger 1890: 274 + +. + + + + + +Cancellaria callosa +Ptsch + +,— + +Boettger 1902: 38 + +. + + + + + +Cancellaria +( +Merica +) +callosa +Partsch + +— + +Sieber 1936: 79 + +. + + + + + +Cancellaria +( +Merica +) +callosa +Ptsch. + +— + +Sieber 1956: 245 + +. + + + + +? + +Cancellaria +( +Merica +) +callosa +Partsch + +— + +Hölzl 1973: 172 + +. + + + + + +Cancellaria +( +Merica +) +callosa +Partsch, 1856 + +— + +Bałuk 2006: 214 + +, pl. 16, fig. 1 [note that the authorship “Partsch” refers to a mansucript name]. + + + + +non + +Merica callosa +Partsch + +— + +Friedberg 1928: 577 + +, pl. 37, fig. 21. + + + + + + + +Type +material. + +NHM +Vienna +( +Austria +); see below for details + +. + + +Studied material. + +1 spec. +Gainfarn +( +Austria +) +NHMW 2009 + +z0098/0014; + +2 spec. +Steinebrunn +( +Austria +) +NHMW 2009 + + +z0098/0015, +NHMW 1863 + +/0015/0696; + +1 spec. +Niederleis +( +Austria +) +NHMW 1863 + +/0020/0696; + +2 spec. +Forchtenau +( +Austria +) +NHMW 1866 + +/0001/1082; + +4 spec. +Lăpugiu de Sus +( +Romania +) +NHMW 1854 + +/035/0233; + +2 spec. +CoŞteiu de Sus +( +Romania +), +NHMW 1867 + +/0029/0128. + + +Illustrated material. + +Fig. 3J +: +CoŞteiu de Sus +( +Romania +), height: +29.2 mm +, width: +17.8 mm +, +NHMW 1867 + +/ + +0029/0128. +Figs. 5E +1–E +3 +: +syntype +illustrated in +Hörnes +(1854, pl. 34, figs 14a–b), +Gainfarn +( +Austria +), height: +33.6 mm +, width: +22.7 mm +, +NHMW 2009 + + +z0098/0014. +The +specimen is marked with a 14, which indicates that it is the specimen figured by +Hörnes. This +is usually a reliable marker, and it therefore seems that the illustration was strongly idealised. +Figs 5F +1–F +3 +: specimen illustrated in +Hörnes +(1854, pl. 34, figs 15a–b), +Steinebrunn +( +Austria +), height: +26.9 mm +, width: +18.9 mm +, +NHMW 2009 + + +z0098/0015. +Figs 5G +1–G +3 +: specimen illustrated in +Hörnes +(1854, pl. 34, figs 16a–b), +Steinebrunn +( +Austria +), height: +20.2 mm +, width: +13.5 mm +, +NHMW 1863 + +/0015/0696. + + + + +Discussion. +This bulky shell is characterized by an inflated shell and globose last whorl. It develops c. 10–12 blunt axial ribs, which are crossed by a spiral sculpture consisting of numerous spiral threads and few broader primary spirals. These are formed by 2–3 close-spaced spiral threads and amalgamate into a single band especially on the backs of the axial rib. Insignificant growth lines cross the spiral threads and cause a somewhat irregular and finely incised surface of the spirals. The protoconch is available only from a single slightly abraded specimen and suggests a low low dome-shaped morphology consisting of about 2.5 weakly convex whorls with a depressed initial part. The absence of a sutural ramp, the convex whorls, the weak to absent umbilicus, the predominant axial sculpture and the presence of three columellar folds are characteristic for the genus + +Contortia +Sacco, 1894 + +as defined by + +Cahuzac +et al. +(2004) + +and + +Landau +et al. +(2006) + +. + + + +The Burdigalian +shells from the +Colli Torinesi +in +Italy +, treated by +Sacco (1894) +as + +Contortia callosa taurolaevior + +and +C. c. tauroturrita +, differ strongly from the +type +in their sculpture. They lack the characteristic spiral cords and have broader and poorly defined axial ribs + +. + + + + +FIGURE 5. A1–A3. + +Calcarata vindobonensis +( +Hilber, 1892 +) + +, Enzesfeld (Austria), NHMW 1846/0037/0291, lectotype. +B1– B3. + +Bivetiella dertonensis +( +Bellardi, 1841 +) + +, Enzesfeld (Austria), NHMW 1846/0037/0282b. +C1–C3. + +Bivetiella dertonensis +( +Bellardi, 1841 +) + +, Bad Vöslau (Austria), NHMW 2009z0098/0018. +D1–D3. + +Bivetiella dertonensis +( +Bellardi, 1841 +) + +, Enzesfeld (Austria), NHMW 1846/0037/0282a. +E1–E3. + +Contortia callosa +(Hörnes, 1854) + +, Gainfarn (Austria), NHMW 2009z0098/0014, syntype. +F1–F3. + +Contortia callosa +(Hörnes, 1854) + +, Steinebrunn (Austria), NHMW 2009z0098/0015. +G1–G3. + +Contortia callosa +(Hörnes, 1854) + +, Steinebrunn (Austria), NHMW 1863/0015/0696. +H1–H3. + +Contortia fenestrata +( +Eichwald, 1830 +) + +, Enzesfeld (Austria), NHMW 2009z0098/0008. +I1–I3. + +Contortia fenestrata +( +Eichwald, 1830 +) + +, Enzesfeld (Austria), NHMW 2009z0098/0009. + + + + +Distribution. +This species is always rare but was distributed throughout the entire Paratethys. Recently, Landau +et al. +(in prep.) also found + +Contortia callosa + +from the late Middle Miocene or earliest Late Miocene of the +Karaman +Basin in +Turkey +, extending the distribution area of the species into the +Proto +–Mediterranean Sea. + + +The record from +Bavaria +mentioned by +Hölzl (1973) +would extend the range down to the Early Miocene. This record, however, is only given in a list without any description and has to be treated with caution. + + +Paratethys +—Badenian: North Alpine Foreland Basin ( +Austria +: Niederleis); Polish–Carpathian Foredeep ( +Poland +: Korytnica); +Vienna +Basin ( +Austria +: Gainfarn, Steinebrunn); Eisenstadt–Sopron Basin ( +Austria +: Forchtenau); Transylvanian Basin ( +Romania +: Lăpugiu de Sus, CoŞteiu de Sus). + +Proto +–Mediterranean Sea + +—Late Serravallian or Early Tortonian: Karman Basin ( +Turkey +). + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC30AFFDEFF0DE1B5E5EDF8BC.xml b/data/38/72/87/387287FCC30AFFDEFF0DE1B5E5EDF8BC.xml new file mode 100644 index 00000000000..a5b1f1242c7 --- /dev/null +++ b/data/38/72/87/387287FCC30AFFDEFF0DE1B5E5EDF8BC.xml @@ -0,0 +1,204 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + + +Contortia contorta +( +Basterot, 1825 +) + + + + + + + + + +C. contorta +Nob. + +— + +Basterot 1825: 47 + +, pl. 2, figs 3a–b. + + + + + +Cancellaria +( +Merica +) +contorta +Basterot 1825 + +— + +Hölzl 1958: 260 + +, pl. 21, fig. 14. + + + + + +Cancellaria +( +Merica +) +contorta +Basterot + +— + +Hölzl 1973: 172 + +. + + + + + +Cancellaria +( +Merica +) +contorta +Basterot + +— + +Hölzl 1973: 194 + +. + + + + + +Contortia contorta +( +Basterot, 1825 +) + +— + + +Cahuzac +et al. +2004: 254 + + +, figs 8L–U [cum syn.]. + + + + + + +Type +material. + +the whereabouts of the +type +material are unknown; +Davoli (1982) +proposed a Burdilaglian specimen from Saint-Paul-lès-Dax ( +France +) illustrated by +Peyrot (1928) +as plesiotype. + + + + +Discussion. +This species is known in the Paratethys only from +Bavaria +( +Hölzl, 1958 +). The preservation of the material is always rather poor and the identifications have to be considered with caution. In respect to the variability of this species, as presented by + +Cahuzac +et al. +(2004) + +, the Bavarian shells with relatively prominent axial ribs range well within + +C. contorta + +. + + + + +Distribution. +A very common species during the Early Miocene from the North East Atlantic to the Paratethys. + + +North East Atlantic +—Early Miocene: +Aquitaine +Basin ( +France +: +Aquitaine +Basin). + +Proto +–Mediterranean Sea + +— Burdigalian: Colli Torinesi: ( +Italy +). +Paratethys +—Eggenburgian and Ottnangian: North Alpine Foreland Basin (Bavaria: Gernergraben, Kaltenbachgraben). + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC30CFFD8FF0DE6CAE3D8FB9E.xml b/data/38/72/87/387287FCC30CFFD8FF0DE6CAE3D8FB9E.xml new file mode 100644 index 00000000000..9516453ac8b --- /dev/null +++ b/data/38/72/87/387287FCC30CFFD8FF0DE6CAE3D8FB9E.xml @@ -0,0 +1,76 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Bivetiella +Wenz, 1943 + + + + + + + + + +Type +species: + +by original designation, + +Cancellaria similis +Sowerby, 1833 + +. +Recent +, north– +western Africa + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC30DFFD9FF0DE024E3FFFA28.xml b/data/38/72/87/387287FCC30DFFD9FF0DE024E3FFFA28.xml new file mode 100644 index 00000000000..5b806161382 --- /dev/null +++ b/data/38/72/87/387287FCC30DFFD9FF0DE024E3FFFA28.xml @@ -0,0 +1,76 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Aneurystoma +Cossmann, 1899 + + + + + + + + + +Type +species: + +by original designation, + +Cancellaria dufourii +Grateloup, 1832 + +. +Early Miocene +, +France + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC30FFFDBFF0DE352E363F916.xml b/data/38/72/87/387287FCC30FFFDBFF0DE352E363F916.xml new file mode 100644 index 00000000000..543f8fc2552 --- /dev/null +++ b/data/38/72/87/387287FCC30FFFDBFF0DE352E363F916.xml @@ -0,0 +1,76 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Calcarata +Jousseaume, 1887b + + + + + + + + + +Type +species: + +by original designation, + +Voluta calcarata +Brocchi, 1814 + +. +Pliocene +, +Italy + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC311FFC5FF0DE68FE34AFBC2.xml b/data/38/72/87/387287FCC311FFC5FF0DE68FE34AFBC2.xml new file mode 100644 index 00000000000..d8f8e021749 --- /dev/null +++ b/data/38/72/87/387287FCC311FFC5FF0DE68FE34AFBC2.xml @@ -0,0 +1,76 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Pseudobabylonella +Brunetti, Della Bella, Forli & Vecchi, 2009 + + + + + + + + + +Type +species: + +by original designation, + +Cancellaria minima +Reeve, 1856 + +. +Recent +, +Madeira + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC312FFC6FF0DE05CE795FA31.xml b/data/38/72/87/387287FCC312FFC6FF0DE05CE795FA31.xml new file mode 100644 index 00000000000..e5ef688d19d --- /dev/null +++ b/data/38/72/87/387287FCC312FFC6FF0DE05CE795FA31.xml @@ -0,0 +1,74 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Cancellicula +Tabanelli, 2008 + + + + + + + + +Type +species: + +by original designation, + +Cancellaria +( +Narona +) +Dregeri +Hoernes & Auinger, 1890 + +. Middle Miocene, Paratethys Sea. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC313FFC7FF0DE415E56BFE78.xml b/data/38/72/87/387287FCC313FFC7FF0DE415E56BFE78.xml new file mode 100644 index 00000000000..c8ca96ce9c2 --- /dev/null +++ b/data/38/72/87/387287FCC313FFC7FF0DE415E56BFE78.xml @@ -0,0 +1,79 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Brocchinia +Jousseaume, 1887b + + + + + + + + +Type +species: + +by subsequent designation of +Sacco, 1894 +, + +Voluta mitraeformis +Brocchi, 1814 + +(non + +Voluta mitraeformis +Lamarck, 1811 + +). Pliocene, +Italy +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC315FFC1FF0DE339E34DF908.xml b/data/38/72/87/387287FCC315FFC1FF0DE339E34DF908.xml new file mode 100644 index 00000000000..0ccb0fb9855 --- /dev/null +++ b/data/38/72/87/387287FCC315FFC1FF0DE339E34DF908.xml @@ -0,0 +1,76 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Bonellitia +Jousseaume, 1887b + + + + + + + + + +Type +species: + +by original designation, + +Cancellaria bonellii +Bellardi, 1841 + +. +Pliocene +, +Italy + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC315FFC1FF0DE41DE3C7FE55.xml b/data/38/72/87/387287FCC315FFC1FF0DE41DE3C7FE55.xml new file mode 100644 index 00000000000..b130ba41efd --- /dev/null +++ b/data/38/72/87/387287FCC315FFC1FF0DE41DE3C7FE55.xml @@ -0,0 +1,76 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Admetula +Cossmann, 1899 + + + + + + + + + +Type +species: + +by original designation, + +Buccinum evulsum +Solander, 1766 + +. +Eocene +, +England + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC315FFC1FF0DE775E553FA69.xml b/data/38/72/87/387287FCC315FFC1FF0DE775E553FA69.xml new file mode 100644 index 00000000000..7ac872a7185 --- /dev/null +++ b/data/38/72/87/387287FCC315FFC1FF0DE775E553FA69.xml @@ -0,0 +1,339 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + + +Admetula serrata +( +Bronn, 1831 +) + + + + + + + + + + +Cancellaria serrata +Bronn, 1831: 44 + + +. + + + + + +Cancellaria +( +Bonellitia +) +serrata +(Bronn) + +— + +Sacco 1894: 43 + +, pl. 3, figs 5–10. + + + + + + +Cancellaria brandenburgi +Boettger 1902 +: p. 38 + + +. + + + + + +Cancellaria brandenburgi +Bttgr + +— + +Boettger 1906: 50 + +. + + + + + +Cancellaria brandenburgi +Boettger + +— + +Zilch 1934: 260 + +, pl. 17, fig. 22. + + + + + +Bonellitia serrata +( +Bronn, 1831 +) + +— + +Chirli 2002: 77 + +, pl. 37, figs 9–16 [cum syn]. + + + + + +Admetula serrata +( +Bronn, 1831 +) + +— + + +Landau +et al. +2006: 85 + + +, pl. 8, figs 5–6 [cum syn]. + + + + + +Bonellitia serrata +( +Bronn, 1831 +) + +— + +Chirli & Richard 2008: 56 + +, pl. 11, fig. 3. + + + + + +Bonellitia serrata +( +Bronn, 1831 +) + +— + +Sosso & Dell’Angelo 2010: 43 +, p. 60 + +unnumbered fig. top row middle. + + + + + +Bonellitia serrata +( +Bronn, 1831 +) + +— + +Caprotti 2011: 73 + +pars [non figs 9O–P + +Ovilia +cf. +andaluciensis +(Landau, 1984) + +]. + + + + + + + +Type +material. + +The whereabouts of the +types +from the +Pliocene +of +Italy +are unknown ( +Davoli 1982 +) + +. + + +Studied material. + +10 specimens +from +Bologna +and +Modena +( +Italy +) +NHMW 1863 + +/0023/0067. + + + + +Discussion. +When describing + +Cancellaria brandenburgi + +as a new species, +Boettger (1902) +already recognised the similarity with + +Cancellaria serrata +Bronn, 1831 + +and based his species on the more slender shell. The shape of + +Admetula serrata +( +Bronn, 1831 +) + +, however, is variable and comprises bulky and slender shells (see +Chirli 2002 +). Therefore, we follow + +Landau +et al. +(2006) + +and treat Boettger’s species as a synonym of + +Admetula serrata +( +Bronn, 1831 +) + +. See +Zilch (1934) +for an illustration of a Paratethyan specimen of that species. + + + + +Distribution. +The species appears during the Burdigalian in the +Proto +–Mediterranean Sea ( +Sacco 1894 +) and spreads into the Paratethys during the early Middle Miocene. It seems to retreat from the Paratethys already during the Serravallian. It is quite common during the Late Miocene of the +Proto +–Mediterranean Sea and experiences its maximum distribution during the Pliocene, when it is known also from the North East Atlantic ( +Spain +) and the North Sea Basin (Harmer 1916). It finally, disappears in the Mediterranean Sea during the Piacenzian (Pliocene) ( + +Landau +et al. +2006 + +). + + +Paratethys +—early and middle Badenian: +Vienna +Basin ( +Austria +: Baden–Sooss), Transylvanian Basin ( +Romania +: CoŞteiu de Sus). + +Proto +–Mediterranean Sea + +—Burdigalian ( +Italy +: Colli Torinesi), Tortonian ( +Italy +: Montegibbio, Stazzano, Sant’Agatha), Early Pliocene ( +Spain +: Estepona; +France +: Roussillon; +Italy +), Piacenzian ( +Italy +). +North Sea +—Early Pliocene ( +Great Britain +). + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC320FFF4FF0DE210E5E7F87D.xml b/data/38/72/87/387287FCC320FFF4FF0DE210E5E7F87D.xml new file mode 100644 index 00000000000..7362e6c0b59 --- /dev/null +++ b/data/38/72/87/387287FCC320FFF4FF0DE210E5E7F87D.xml @@ -0,0 +1,63 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + + +Cancellaria macrostoma +du Bois de Montpéreux, 1831 + + + + + +The illustration in +du Bois de Montpéreux (1831) +shows a rissooid gastropod as already recognised by Pusch (1837). + + + +Polish–Carpathian Foredeep, Badenian. + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC320FFF4FF0DE7CAE310FC9D.xml b/data/38/72/87/387287FCC320FFF4FF0DE7CAE310FC9D.xml new file mode 100644 index 00000000000..e785139d0b4 --- /dev/null +++ b/data/38/72/87/387287FCC320FFF4FF0DE7CAE310FC9D.xml @@ -0,0 +1,76 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Tritonoharpa +Dall, 1908 + + + + + + + + + +Type +species: + +by original designation, + +Tritonoharpa vexillata +Dall, 1908 + +. +Recent +, +Eastern Pacific + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC321FFF4FF0DE3B7E64EFD84.xml b/data/38/72/87/387287FCC321FFF4FF0DE3B7E64EFD84.xml new file mode 100644 index 00000000000..e3a76094456 --- /dev/null +++ b/data/38/72/87/387287FCC321FFF4FF0DE3B7E64EFD84.xml @@ -0,0 +1,260 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + + +Ventrilia trochlearis +( +Faujas, 1817 +) + + + + + + + + + + +Cancellaria trochlearis +Faujas, 1817: 197 + + +, pl. 10, figs 2a–b. + + + + + +Cancellaria +( +Trigonostoma +) +trochlearis disparstriata + +nov. var. +— + +Hölzl 1958: 257 + +, pl. 21, fig. 11. + + + + + +Cancellaria +( +Trigonostoma +) +trochlearis gravecostata + +nov. var. +— + +Hölzl 1958: 257 + +, pl. 21, figs 12–12. + + + + + +Trigonostoma +( +Tr. +) +trochlearis disparstriata +(Hoelzl) + +— + +Hölzl 1973: 172 + +. + + + + + +Trigonostoma +( +Tr. +) +trochlearis gravecostata +(Hoelzl) + +— + +Hölzl 1973: 172 + +. + + + + + +Ventrilia trochlearis +( +Faujas, 1817 +) + +— + + +Cahuzac +et al. +2004: 224 + + +, figs 3P–S [cum syn.]. + + + + + + + +Type +material. + +the +type +from the +Early Miocene +of +France +is lost ( + +Cahuzac +et al. +, 2004 + +) + + + + + +Discussion. +Hölzl (1958) +introduced +disparstriata +and +gravecostata +as +variety names +of + +Ventrilia trochlearis +( +Faujas, 1817 +) + +for shells from the Early Miocene of +Bavaria +. The preservation of that material is poor but the general shape and sculpture agree with French specimens of + +Ventrilia trochlearis +( +Faujas, 1817 +) + +as described by +Peyrot (1928) +and + +Cahuzac +et al. +(2004) + +. For an illustration of the Paratethyan representatives see +Hölzl (1958) +. + + + + +Distribution. +This species is widespread during the Early Miocene from the North East Atlantic to the Paratethys. + + +North East Atlantic +— + +Early Miocene: +Aquitaine +Basin ( +France +: +Aquitaine +Basin) + +. + + + +Proto +–Mediterranean Sea + +—Burdigalian: Colli Torinesi: ( +Italy +). + + +Paratethys +— + +Eggenburgian and Ottnangian: +North Alpine Foreland Basin +( +Bavaria +: Gernergraben, Kaltenbachgraben) + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC321FFF5FF0DE5EDE316FF67.xml b/data/38/72/87/387287FCC321FFF5FF0DE5EDE316FF67.xml new file mode 100644 index 00000000000..db8515c7b5e --- /dev/null +++ b/data/38/72/87/387287FCC321FFF5FF0DE5EDE316FF67.xml @@ -0,0 +1,70 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Ventrilia +Jousseaume, 1887a + + + + + + + + +Type +species: + +by original designation, + +Cancellaria tenera +Philippi, 1848 + +. Recent, Caribbean Sea. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC323FFF7FF0DE431E6BFFE5C.xml b/data/38/72/87/387287FCC323FFF7FF0DE431E6BFFE5C.xml new file mode 100644 index 00000000000..f1bd50328b3 --- /dev/null +++ b/data/38/72/87/387287FCC323FFF7FF0DE431E6BFFE5C.xml @@ -0,0 +1,68 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + + +Cancellaria effosa +Handmann, 1882 + + + + + +A valid Latin description is presented by +Handmann (1882) +but no illustration is provided. The material is lost and we consider this taxon a +nomen dubium +. + + + + +Vienna +Basin, Badenian. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC323FFF7FF0DE5EDE6BFFE8F.xml b/data/38/72/87/387287FCC323FFF7FF0DE5EDE6BFFE8F.xml new file mode 100644 index 00000000000..d4ca3529474 --- /dev/null +++ b/data/38/72/87/387287FCC323FFF7FF0DE5EDE6BFFE8F.xml @@ -0,0 +1,68 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + + +Cancellaria varicosissima +Handmann, 1882 + + + + + +A valid Latin description is presented by +Handmann (1882) +but no illustration is provided. The material is lost and we consider this taxon a +nomen dubium +. + + + + +Vienna +Basin, Badenian. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC328FFFCFF0DE5EDE357FF67.xml b/data/38/72/87/387287FCC328FFFCFF0DE5EDE357FF67.xml new file mode 100644 index 00000000000..329533ae017 --- /dev/null +++ b/data/38/72/87/387287FCC328FFFCFF0DE5EDE357FF67.xml @@ -0,0 +1,76 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Tribia +Jousseaume, 1887b + + + + + + + + + +Type +species: + +by original designation, + +Tribia angasi +Crosse, 1863 + +. +Recent +, +western Africa + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC32BFFFFFF0DE119E31BFB53.xml b/data/38/72/87/387287FCC32BFFFFFF0DE119E31BFB53.xml new file mode 100644 index 00000000000..b19a56b46de --- /dev/null +++ b/data/38/72/87/387287FCC32BFFFFFF0DE119E31BFB53.xml @@ -0,0 +1,76 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Trigonostoma +Blainville, 1827 + + + + + + + + + +Type +species: + +by monotypy, + +Delphinula trigonostoma +Lamarck, 1822 + +. +Recent +, +Indo–West Pacific + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC32DFFF9FF0DE3F3E363F975.xml b/data/38/72/87/387287FCC32DFFF9FF0DE3F3E363F975.xml new file mode 100644 index 00000000000..aa88dc6c301 --- /dev/null +++ b/data/38/72/87/387287FCC32DFFF9FF0DE3F3E363F975.xml @@ -0,0 +1,76 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Sveltia +Jousseaume, 1887b + + + + + + + + + +Type +species: + +by original designation, + +Voluta varricosa +Brocchi, 1814 + +, +Pliocene +, +Italy + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC332FFF9FF0DE397E31BFD34.xml b/data/38/72/87/387287FCC332FFF9FF0DE397E31BFD34.xml new file mode 100644 index 00000000000..83099c5e42d --- /dev/null +++ b/data/38/72/87/387287FCC332FFF9FF0DE397E31BFD34.xml @@ -0,0 +1,118 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Steiningeriella + +nov. gen. + + + + + + + + +Type +species: + + +Cancellaria hebertiana +Hörnes, 1856 + +. +Middle Miocene +, +Austria + +. + + + + +Derivatio nominis: +in honor of the Paleontologist Fritz Steininger + + + + +Diagnosis. +Medium sized, slender shell with allometric growth, expressed by rapidly increasing height of the whorls. Spire whorls are smooth and moderately convex; a weak concavity appears in the adapical third of the last whorl, causing a sigmoidal outline of the outer lip. A deeply canaliculated suture separates the whorls. Aperture elongate with slightly thickened outer lip, bearing lirae, which extend far into the shell. Due to the deep suture and the concave posterior part of the whorl, abapical portion of outer lip flared. The straight columella bears three strong, only slightly oblique columellar folds, of which the middle one is most prominent. A fourth, twisted fold terminates the columella and borders the indistinct siphonal canal. Parietal and columellar calluses well delimited, adherent, columellar callus greatly thickened. The umbilicus is reduced to a narrow fissure covered by the columellar callus. The protoconch is unknown. + + + + +Discussion. +This genus comprises only the +type +species so far. This extremely rare species was placed in +Nevia +Jousseaume, 1887b +by +Sacco (1894) +. The +type +species of +Nevia +is the Recent Australian + +Cancellaria spirata +Lamarck, 1822 + +. +Garrard (1975) +gives a diagnosis of the genus: “Shell medium, solid, ovate, deeply canaliculated, aperture widely oblong, tapering either end; outer-lip acute, lirate internally; columella straight with 3 oblique plaits; axially ribbed in early whorls, ribs tending later to flatten or disappear. Deep canal at top of shoulder is main distinguishing feature.” This illustrates that + +Cancellaria hebertiana +Hörnes, 1856 + +cannot be placed in +Nevia +. It differs in the elongate shell, the concave posterior part of the last whorl, the absence of any axial sculpture and the presence of the twisted fourth columellar fold. Only the deep suture appears in both taxa. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC333FFE7FF0DE6D5E3F3FB9F.xml b/data/38/72/87/387287FCC333FFE7FF0DE6D5E3F3FB9F.xml new file mode 100644 index 00000000000..b88c0144e08 --- /dev/null +++ b/data/38/72/87/387287FCC333FFE7FF0DE6D5E3F3FB9F.xml @@ -0,0 +1,76 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Solatia +Jousseaume, 1887b + + + + + + + + + +Type +species: + +by original designation, + +Buccinum piscatorium +Gmelin, 1791 + +. +Recent +, +western Africa + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC339FFECFF0DE083E57AFCEC.xml b/data/38/72/87/387287FCC339FFECFF0DE083E57AFCEC.xml new file mode 100644 index 00000000000..955d7d9dca2 --- /dev/null +++ b/data/38/72/87/387287FCC339FFECFF0DE083E57AFCEC.xml @@ -0,0 +1,287 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + + +Scalptia dertocosticillata +( +Sacco, 1894 +) + +nov. comb. + + + + + + + + + +Cancellaria +( +Trigonostoma +) +imbricatum +var. +dertocosticillata +Sacco, 1894: 13 + + +; pl. 1, fig. 31. + + + + + +Trigonostoma puschi +R. Hoern. + +i Auing.— + +Friedberg 1914: 248 + +, pl. 15, fig. 12. + + + + + +Trigonostoma puschi +(R. Hoernes et Auinger, 1879) + +— + + +Zelinskaya +et al. +1968: 216 + + +, pl. 49, figs 33–34. + + + + + +Trigonostoma imbricatum +var. +dertocosticillata +Sacco, 1894 + +— + + +Ferrero Mortara +et al. +1984: 161 + + +, pl. 29, fig. 3. + + + + + +Trigonostoma puschi +( +Hoernes & Auinger, 1890 +) + +— + +Bałuk 1997: 45 + +, pl. 15, figs 4–5. + + + + + +Type material. + +syntype +BS.045.01.030, +Museo Regionale di Scienci Naturali +, +Torino +( +Italy +); +Stazzano +( +Italy +), +Tortonian +( +Late Miocene +) [data from Ferrero-Mortara +et al. +1984] + +. + + + + +Discussion. +This species was frequently intermingled with + +Scalptia polonica +(Pusch, 1837) + +. The specimens presented by +Bałuk (1997) +, however, are more similar to + +Scalptia dertocosticillata +( +Sacco, 1894 +) + +from the Tortonian of +Italy +. Both species develop a comparable outline with a slight concavity below the shoulder and a somewhat inflated lower third of the last whorl. A marked shoulder angulation causes a terraced spire with deep cavities between the axial ribs on the narrow shelf. The axial ribs are prominent on the spire whorls and become slightly less distinct on the last whorl. The spiral cords cross the axials, and a secondary spiral rib is intercalated in the interspaces, giving the surface a slightly scaley appearance. + + +Sacco (1894) +described this species as variety of + +Cancellaria imbricata +Hörnes, 1854 + +, which develops a much wider umbilicus. + +Scalptia burdigalensis +( +Peyrot, 1928 +) + +, from the Burdigalian of the +Aquitaine +Basin, might be an ancestor of the Paratethyan species. It differs mainly in the wider umbilicus and lacks the secondary spiral ribs (see + +Cahuzac +et al. +2004 + +). The placement of this species in the genus + +Scalptia + +is based mainly on the similarity with this French species but will need further confirmation. + + +Despite the morphologic similarity between the Paratethyan species and the Italian +type +, doubts remain if they are really conspecific. The Paratethyan shells are known so far only from the Polish–Carpathian Foredeep, which was repeatedly isolated from other Paratethyan basins, resulting in an increased endemism (e.g. within nassariids +Harzhauser & Kowalke 2004 +). Thus, the similarity with + +Scalptia dertocosticillata +( +Sacco, 1894 +) + +might represent a convergence as well. + + +A dubious Early Miocene record is mentioned by + +Steininger +et al. +(1971) + +from Lipovany in +Slovakia +as + +Cancellaria +( +Trigonostoma +) +puschi + +. +The authors refer to the specimens illustrated by +Friedberg (1914) +, which are considered herein as + +Scalptia +cf. +dertocosticillata +( +Sacco, 1894 +) + +. The whereabouts of the Slovak material are unclear and the record lacks a description and illustration. Therefore, we refrain from listing it in the chresonynmy. + + + + +Distribution. +Known from the Badenian of the north–eastern Paratethys and from the Middle–Late Miocene of the +Proto +–Mediterranean Sea. + + +Paratethys +—Badenian: Polish–Carpathian Foredeep ( +Poland +: Korytnica, Piṅczów, Zglobice). + +Proto +–Mediterranean Sea + +—Tortonian: Po Basin ( +Italy +: Stazzano, Montegibbio, Sant’Agata). Late Serrvallian–Early Tortonian: +Karaman +Basin ( +Turkey +, BL coll.). + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC339FFEDFF0DE031E3A5FA3B.xml b/data/38/72/87/387287FCC339FFEDFF0DE031E3A5FA3B.xml new file mode 100644 index 00000000000..27efd2cd862 --- /dev/null +++ b/data/38/72/87/387287FCC339FFEDFF0DE031E3A5FA3B.xml @@ -0,0 +1,76 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Scalptia +Jousseaume, 1887b + + + + + + + + + +Type +species: + +by original designation, + +Cancellaria obliquata +Lamarck, 1822 + +. +Recent +, +Indo–West Pacific + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC339FFEDFF0DE5EDE321FB64.xml b/data/38/72/87/387287FCC339FFEDFF0DE5EDE321FB64.xml new file mode 100644 index 00000000000..250ea00f838 --- /dev/null +++ b/data/38/72/87/387287FCC339FFEDFF0DE5EDE321FB64.xml @@ -0,0 +1,265 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + + +Petitina angulata +( +Sieber, 1936 +) + +nov. comb. + + + + + + +Figs 8A +1–A +3 +, +8B +1–B +3 + + + + + + +Cancellaria inermis +Pusch + +— + +Franzl 1870: 49 + +. + + + + + +Cancellaria +( +Sveltia +) +inermis +Pusch var. +angulata + +n. v. + +Sieber 1936: 98 + +, pl. 3, figs 7a–b [non + +Cancellaria angulata +Eichwald, 1830 + +]. + + + + + +Narona +( +Sveltia +) +inermis +(Pusch, 1837) + +— + +Harzhauser 2002: 110 + +[non + +Petitina inermis +(Pusch, 1837) + +]. + + + + + + + +Type +material. + +NHM +Vienna +( +Austria +); see below for details + +. + + +Studied material. + +3 spec. +Niederkreuzstetten +( +Austria +) +NHMW 1849 + +/0023/0016. + + +Illustrated material. + +Figs 8A +1–A +3 +: specimen illustrated in +Sieber (1936 +, pl. 3, figs 7a–b), +NHMW 1849 +/0023/ 0016, +Niederkreuzstetten +( +Austria +), height: +28.7 mm +, width: +18.5 mm +, +syntype + +, +Figs 8B +1–B +3 +: height: +24.8 mm +, width: +14.8 mm +, +syntype +. + + + + +Description: +A medium sized cancellariid with gradate spire and elongated barrel-shaped last whorl. The spire whorls are high with nearly flat flanks, bulgy shoulder and narrow subsutural swelling. The high last whorl has subparallel flanks and a shoulder swelling that forms a narrow sutural ramp. A very weak concavity appears directly below the shoulder. The shell surface is smooth except for blunt growth lines and faint axial ribs on the early spire whorls. Base slowly contracting. A weak central columellar fold is adjoined by a faint anterior fold; columella straight. Columellar callus thickened grading into a prominent parietal callus. The outer lip is only fragmentarily preserved; no lirae or denticles are developed; no umbilicus. + + + + +Discussion. +The thin outer lip, the moderately wide aperture with very prominent inner lip and the weak central columellar fold place the species in + +Petitina + +and points to a relation to + +Petitina inermis +(Pusch, 1837) + +. Consequently, +Sieber (1936) +introduced the name + +angulata + +as +variety name +of + +Cancellaria inermis +Pusch, 1837 + +for these specimens. This species, however, differs from + +Petitina inermis +(Pusch, 1837) + +in its gradate spire, barrel-shaped last whorl, smaller size, the presence of a callus and the absence of axial sculpture, justifying a separation on species level. The name “ + +angulata + +” is preoccupied by + +Cancellaria angulata +Eichwald (1830) + +for a shell from +Poland +, which was later transferred to + +Turbinella + +by +Eichwald (1853) +. As these taxa have not been considered to be congeneric after 1899, no replacement is needed in accordance with ICZN 23.9.5 and the valid cyronym is + +Petitina angulata +( +Sieber, 1936 +) + +. + + + + +Distribution. +This rare species is known so far only from the Karpatian (Late Burdigalian) of the Paratethys Sea. + + +Paratethys +—Karpatian: Waschberg–Zdanice Unit ( +Austria +, Niederkreuzstetten). + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC33CFFE8FF0DE1F2E301FB76.xml b/data/38/72/87/387287FCC33CFFE8FF0DE1F2E301FB76.xml new file mode 100644 index 00000000000..80a4bd1794e --- /dev/null +++ b/data/38/72/87/387287FCC33CFFE8FF0DE1F2E301FB76.xml @@ -0,0 +1,78 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Perplicaria +Dall, 1890 + + + + + + + + + +Type +species: + +by original designation, + +Perplicaria perplexa +Dall, 1890 + +. +Pliocene +, +Florida +, +USA + +. + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC33CFFE8FF0DE5EDE3D2FBA7.xml b/data/38/72/87/387287FCC33CFFE8FF0DE5EDE3D2FBA7.xml new file mode 100644 index 00000000000..374d523e727 --- /dev/null +++ b/data/38/72/87/387287FCC33CFFE8FF0DE5EDE3D2FBA7.xml @@ -0,0 +1,158 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + + +Ovilia + +? sp. + + + + + + +Figs 7E +1–E +2 + + + + +Illustrated material. +Figs 7H +1–H +2 +: Mörtersdorf ( +Austria +), height: +30 mm +, width: +26 mm +, private collection Anton and Thomas Breitenberger (Bad Vöslau and Pottenstein, +Austria +). + + + + +Description. +Globular shell with low, gradate spire and large, convex last whorl. A shoulder appears already on early whorls and separates a flat sutural shelf from the flanks. Sculpture consisting of 13 low fold-like axial ribs overrun by about ten flattened spiral cords, with broad, horizontally elongate nodes developed at the intersections. These are most prominent along the shoulder. Up to three wavy secondary spiral threads are intercalated between the adapical five primary cords, whilst only one (or no) threads are intercalated between the cords on the base. Aperture and base obscured by sediment. + + + + +Discussion. +Only a single specimen is available and the aperture is unknown. Therefore, even the generic assignment remains doubtful. Although some specimens of the Early Miocene + +Ovilia doliolaris + +have tendencies to develop rugose spiral ribs, as evident from the illustration in +Basterot (1825) +, none displays such a conspicuous sculpture. The weak suture of the Austrian shell allows a clear separation from the + +O doliolaris + +group and the newly described + +O. breitenbergerorum + +, which occurs at the same locality. + + +A second group of species, which we provisionally include in the genus + +Ovilia + +, have axial sculpture, albeit weak, much less conspicuous spiral cords and a less deeply canaliculate suture. This group is characterised by + +O. excassidea +( +Sacco, 1894 +) + +in the Miocene and + +O. cassidea +( +Brocchi, 1814 +) + +and + +O. andaluciensis +Landau, +1984 + +in the Pliocene. The Austrian shell resembles + +O. excassidea + +in outline and suture +type +and might represent an ancestral form of this Middle Miocene species. The sculpture of both species is also comparable. Differences are the blunt nodes and densely spaced spiral ribs of the Early Miocene Austrian shell, as opposed to the much narrower spiral cords of + +O. excassidea + +, and the poorly defined axial ribs, whilst + +O. excassidea + +has a distinct axial sculpture. + + + + +Distribution. +A rare species, which is only known from the Paratethys Sea. + + +Paratethys +—Eggenburgian (Early Burdigalian): Bohemian Massif ( +Austria +: Mörtersdorf). + + + + \ No newline at end of file diff --git a/data/38/72/87/387287FCC33FFFEBFF0DE1FDE4B8FA4E.xml b/data/38/72/87/387287FCC33FFFEBFF0DE1FDE4B8FA4E.xml new file mode 100644 index 00000000000..c425e3e906f --- /dev/null +++ b/data/38/72/87/387287FCC33FFFEBFF0DE1FDE4B8FA4E.xml @@ -0,0 +1,112 @@ + + + +A revision of the Neogene Cancellariid Gastropods of the Paratethys Sea 3472 + + + +Author + +Harzhauser, Mathias + + + +Author + +Landau, Bernard + +text + + +Zootaxa + + +2012 + +2012-09-07 + + +3472 + + +1 +71 + + + +journal article +1175­5334 +6B088E9E-EAD4-4B8B-938B-178ADACF4CC3 + + + + + + +Genus + +Petitina +Harzhauser & Landau + +nov. nom. + + + + += +Inermia +Korobkov, 1955 +[non +Inermia +Poey, 1860] + + + + + + +Type +species. + + +Cancellaria inermis +Pusch, 1837 + +by subsequent designation of +Korobkov (1955) +. +Middle Miocene +, +Poland + +. + + + + +Discussion. + +Cancellaria inermis +Pusch, 1837 + +was selected as +type +species of the genus +Inermia +by +Korobkov (1955) +—a genus name that was already preoccupied for the fish genus +Inermia +Poey, 1860. This lapsus was recognised by +Petit and Harasewych (2005) +without designating a replacement name. Therefore, in honour of Richard E. Petit, we propose + +Petitina + +as new genus name for the preoccupied +Inermia +. + + + + \ No newline at end of file diff --git a/data/38/72/CC/3872CC55FB492440205F83FEFBE4FCC6.xml b/data/38/72/CC/3872CC55FB492440205F83FEFBE4FCC6.xml new file mode 100644 index 00000000000..c30a95683c3 --- /dev/null +++ b/data/38/72/CC/3872CC55FB492440205F83FEFBE4FCC6.xml @@ -0,0 +1,287 @@ + + + +Two new species of Exetastes (Hymenoptera: Ichneumonidae: Banchinae) from the Peruvian Andes + + + +Author + +Reshchikov, Alexey +C1DCCD18-C213-4454-99BB-D0BACA05D7BD +Institute of Eastern-Himalaya Biodiversity Research, Dali University, Dali, Yunnan, China. +alexey.reshchikov@eastern-himalaya.cn + + + +Author + +Alvarado, Mabel +969AA574-A398-4087-BCF9-98CB8ABDC91F +Universidad Nacional Mayor de San Marcos, Museo de Historia Natural, Departamento de Entomología, Av. Arenales 1256 Jesús María, Lima 14, Peru. +malvaradog@unmsm.edu.pe + +text + + +European Journal of Taxonomy + + +2022 + +2022-03-22 + + +806 + + +1 + + +52 +63 + + + + +http://zoobank.org/f1739941-a6bd-4330-88c1-bc6f9392d591 + +journal article +20122 +10.5852/ejt.2022.806.1701 +f9bcd4f5-c05e-4e54-ab4c-d3ba812646d2 +2118-9773 +6384512 +F1739941-A6BD-4330-88C1-BC6F9392D591 + + + + + + +Exetastes andensis + +sp. nov. + + + + + + +urn:lsid:zoobank.org:act: +F4191926-8B12-454B-B4D6-F1F0C43521E8 + + + +Figs 2 +, +4B + + + + + +Etymology + + + +The specific name is the Latin adjective ʻ + +andensis + +ʼ and refers to this species’ Andean distribution. + + + + + +Type material + + + + + +Holotype + +PERU +• + +; +Cusco Region +, +Wayquecha Biological Station +, +Andean Cloud Forest +; +13.17448° S +, +71.58691° W +; + +2865 m +a.s.l. + +; + +21 Jul.–8 Aug. 2014 + +; +Malaise trap +; +J. Bergsten +et al. +leg.; +MUSM +. + + + + + +Paratypes + +PERU +• +1 ♀ +; same collection data as for holotype; +MUSM + +• + +1 ♀ +; same collection data as for holotype but +13.18333° S +, +71.58691° W +; + +2865 m +a.s.l. + +; +MUSM + +• + +1 ♀ +; same locality as for holotype but +13.183° S +, +71.583° W +; + +2800 m +a.s.l. + +; + +11 Sep. 2007 + +; +sweep net +; +C. Castillo +leg.; +MUSM + +. + + + + + +Description + + + +Female +( +holotype +) + + +MEASUREMENT. Fore wing length +12 mm +. + + +HEAD. Clypeus, in profile, basally weakly convex, subapically slightly concave; 1.5 times as wide as high. Mandible ( +Fig. 2D +) with upper tooth large, obliquely chisel-shaped, and weakly subdivided; basally coriaceous and punctate, smooth on apical third. Malar space 0.7 times basal width of mandible. Face, frons, vertex, and gena finely granulate, matt, finely and somewhat indistinctly punctate. Face ( +Fig. 2D +) with weak median convexity. Gena, in lateral view, 0.4 times as long as compound eye.Antenna ( +Fig. 2A +) setaceous with 46 flagellomeres; ratio of length vs width from second to fourth flagellomeres: 2.8:2.5:2.5, ratios of those around 0.7 of way along flagellum: 1.2, ratio of subapical flagellomere: 1.2. Ocellar-ocular distance 1.5 times maximum diameter of lateral ocellus ( +Fig. 2B +). + + +MESOSOMA. Mesosoma entirely granulate, matt, mostly finely and densely punctate. Epomia and notaulus absent ( +Fig. 2B +). Scutellum ( +Fig. 4B +) pyramidal in profile. Subalar prominence strongly raised and sharply rounded. Metapleuron evenly convex, with submetapleural carina moderately raised, extending about 0.6 of length of pleuron. Propodeum ( +Fig. 2E +) granulate, with reticulate sculpture; pleural carina absent anteriorly, strong posteriorly. Fore tibia slender, unspecialized. Hind femur 5.8 times as long as its maximum width in lateral view. Tarsal claw simple. Fore wing with 3rs-m meeting Rs without joining 2rs-m, enclosing an areolet that is narrowly truncate above, with abscissa of M between 2rs-m and 2m-cu as long as abscissa of M between 2m-cu and 3rs-m; cu-a more or less opposite base of Rs and M. + + + +Fig. 2. + +Exetastes andensis + +sp. nov. +, holotype, ♀ (MUSM). +A +. Habitus, in lateral view. +B +. Head, in dorsal view and mesoscutum. +C +. T1–2. +D +. Face. +E +. Propodeum. +F +. Ovipositor. B–F not to scale. + + + +METASOMA. T1 2.8 times as long as posteriorly wide; with spiracle positioned in anterior 0.46; granulate, matt, mostly finely and densely punctate ( +Fig. 2C +). T2 0.9 times as long as posteriorly wide; granulate, matt, mostly finely and densely punctate. Ovipositor sheath elongate and slim, with transverse striation on outer surface. Ovipositor ( +Fig. 2F +) projecting beyond apex of subgenital plate by 0.8 times length of hind tibia; stout, compressed, decurved, with subapical notch. + + +COLOR. Coloration reddish-yellow ( +Fig. 2A +), except for following which are marked with black: 15–46 +th +flagellomeres of antenna, teeth of mandibles, frons, groove between postscutellum and propodeum, groove between lower part of mesopleuron and metapleuron ( +Figs 2E +, +4B +), anteroventral part of hind coxa, dorsal part of fifth tarsomere of fore leg, dorsal parts of second to fifth tarsomeres of middle and hind legs, first sternite of metasoma, ventral edges of laterotergites of T2–3, anterolateral part of fifth sternite, anterolateral spots of T4, setae on T4–7, T8 entirely, cerci, ovipositor sheath except for pale apical tip, ovipositor; and following which are marked with bright yellow: 1 +st +–14 +th +flagellomeres of antenna, tip of ovipositor sheath ( +Fig. 2F +); T4–7 and corresponding sternites which are white ( +Fig. 2A +). + + + +Variation + + + +The +paratype +has the scuto-scutellar groove and anterior edge of T5–7 black. + + + + \ No newline at end of file diff --git a/data/38/72/CC/3872CC55FB4B244E20B882E8FE48FC65.xml b/data/38/72/CC/3872CC55FB4B244E20B882E8FE48FC65.xml new file mode 100644 index 00000000000..6a5ed98db4d --- /dev/null +++ b/data/38/72/CC/3872CC55FB4B244E20B882E8FE48FC65.xml @@ -0,0 +1,228 @@ + + + +Two new species of Exetastes (Hymenoptera: Ichneumonidae: Banchinae) from the Peruvian Andes + + + +Author + +Reshchikov, Alexey +C1DCCD18-C213-4454-99BB-D0BACA05D7BD +Institute of Eastern-Himalaya Biodiversity Research, Dali University, Dali, Yunnan, China. +alexey.reshchikov@eastern-himalaya.cn + + + +Author + +Alvarado, Mabel +969AA574-A398-4087-BCF9-98CB8ABDC91F +Universidad Nacional Mayor de San Marcos, Museo de Historia Natural, Departamento de Entomología, Av. Arenales 1256 Jesús María, Lima 14, Peru. +malvaradog@unmsm.edu.pe + +text + + +European Journal of Taxonomy + + +2022 + +2022-03-22 + + +806 + + +1 + + +52 +63 + + + + +http://zoobank.org/f1739941-a6bd-4330-88c1-bc6f9392d591 + +journal article +20122 +10.5852/ejt.2022.806.1701 +f9bcd4f5-c05e-4e54-ab4c-d3ba812646d2 +2118-9773 +6384512 +F1739941-A6BD-4330-88C1-BC6F9392D591 + + + + + + +Exetastes tullu + +sp. nov. + + + + + + +urn:lsid:zoobank.org:act: +22591EEF-C304-4EDD-A772-5D83166F7F16 + + + +Figs 3 +, +4A + + + + + +Etymology + + + +The specific epithet ʻ + +tullu + +ʼ means ʻthinʼ in Quechua, noun in apposition. + + + + + +Type material + + + + + +Holotype + +PERU +• + +; +Cusco Region +, +Wayquecha Biological Station +; +13.175° S +, +71.581° W +; + +2692 m +a.s.l. + +; + +22 Oct. 2007 + +; +Malaise trap +; +C. Castillo +leg.; +MUSM +. + + + + + +Paratype + +PERU +• +1 ♀ +; same collection data as for holotype; +MUSM + +. + + + + + +Description + + + +Female +( +holotype +) + + +MEASUREMENT. Fore wing length +8.2 mm +. + + +HEAD. Clypeus, in profile, basally weakly convex, subapically slightly concave; 1.5 times as wide as high. Mandible with upper mandibular tooth as large as lower tooth, without subdivision; basally coriaceous and punctate, smooth on apical half. Malar space 0.6 times basal width of mandible. Face ( +Fig. 3C +), frons, vertex ( +Fig. 3B +), and gena finely granulate, matt, finely and somewhat indistinctly punctate. Face with weak median convexity. Gena, in lateral view, 0.4 times as long as compound eye. Antenna setaceous with 52 flagellomeres ( +paratype +with 50 flagellomeres); ratio of length vs width from second to fourth flagellomeres: 3.6:3.0:2.9, ratio of those around 0.7 of way along flagellum: 1.5, subapical flagellomere: 1.2. Ocellar-ocular distance 1.9 times maximum diameter of lateral ocellus ( +Fig. 3B +). + + +MESOSOMA. Mesosoma entirely granulate, matt, mostly finely and densely punctate. Epomia absent. Notaulus faint ( +Fig. 3B +). Scutellum, in profile, pyramidal ( +Fig. 4A +). Subalar prominence strongly raised, sharply rounded. Upper half of metapleuron convex, lower half concave, upper margin scrobiculate, with submetapleural carina moderately raised extending about 0.7 of length of pleuron. Propodeum ( +Fig. 3D +) granulate, matt, mostly finely and densely punctate; pleural carina present anteriorly, absent posterior to spiracle. Fore tibia slender, unspecialized. Hind femur 7.9 times as long as its maximum width in lateral view. Tarsal claw simple. Fore wing with 3rs-m meeting Rs without joining 2rs-m, enclosing an areolet that is narrowly truncate above; abscissa of M between 2rs-m and 2m-cu shorter than abscissa of M between 2m-cu and 3rs-m; cu-a distal to base of Rs and M. + + + +Fig. 3. + +Exetastes tullu + +sp. nov. +holotype, ♀ (MUSM). +A +. Habitus, in lateral view. +B +. Head, mesosoma and T1 in dorsal view. +C +. Face. +D +. Propodeum. +E +. Ovipositor. B–F not to scale. + + + +METASOMA. T1 ( +Fig. 3B +) 4.1 times as long as posteriorly wide; with spiracle positioned in anterior 0.46; granulate, shiny, mostly finely and densely punctate. T2 1.8 times as long as posteriorly wide, granulate, shiny, mostly finely and densely punctate. Ovipositor sheath elongate and slim, with transverse striation on outer surface. Ovipositor ( +Fig. 3A, E +) projecting beyond apex of subgenital plate by 1.0 times length of hind tibia; stout, compressed, decurved, with subapical notch. + + +COLOR. Coloration black ( +Fig. 3A +), except for following which are marked with yellow: lower half of clypeus, mandibles (except teeth), facial orbit ( +Fig. 3C +) reaching upwards to lower part of frons, malar space, anterior margin of pronotum, along with its posterior margin dorsally and posterodorsally ( +Fig. 3D +), propleuron, mesoscutum anterolaterally, transverse median stripe on scutellum, anterior edge of mesopleuron, a mark at end of epicnemial carina, subalar prominence, mesepisternum, ventral part of fore coxa, fore and mid femur and tibia ventrally, mid coxa ventrodistally, anterior third of T1 ( +Fig. 3B +), lateral edges and distal edge, T2–4, and sternite 1–5; and following parts which are brown ( +Figs. 3A, 3E +): fore and mid femur dorsally and extreme, fore and mid femur, tibia dorsally, hind femur, hind tibia, tarsomere, and ovipositor. + + + + \ No newline at end of file diff --git a/data/38/72/CC/3872CC55FB4E2442206F8342FE73FDD1.xml b/data/38/72/CC/3872CC55FB4E2442206F8342FE73FDD1.xml new file mode 100644 index 00000000000..9ab55141f2f --- /dev/null +++ b/data/38/72/CC/3872CC55FB4E2442206F8342FE73FDD1.xml @@ -0,0 +1,279 @@ + + + +Two new species of Exetastes (Hymenoptera: Ichneumonidae: Banchinae) from the Peruvian Andes + + + +Author + +Reshchikov, Alexey +C1DCCD18-C213-4454-99BB-D0BACA05D7BD +Institute of Eastern-Himalaya Biodiversity Research, Dali University, Dali, Yunnan, China. +alexey.reshchikov@eastern-himalaya.cn + + + +Author + +Alvarado, Mabel +969AA574-A398-4087-BCF9-98CB8ABDC91F +Universidad Nacional Mayor de San Marcos, Museo de Historia Natural, Departamento de Entomología, Av. Arenales 1256 Jesús María, Lima 14, Peru. +malvaradog@unmsm.edu.pe + +text + + +European Journal of Taxonomy + + +2022 + +2022-03-22 + + +806 + + +1 + + +52 +63 + + + + +http://zoobank.org/f1739941-a6bd-4330-88c1-bc6f9392d591 + +journal article +20122 +10.5852/ejt.2022.806.1701 +f9bcd4f5-c05e-4e54-ab4c-d3ba812646d2 +2118-9773 +6384512 +F1739941-A6BD-4330-88C1-BC6F9392D591 + + + + + +Genus + +Exetastes +Gravenhorst, 1829 + + + + + + + + + +Exetastes +Gravenhorst, 1829: 395 + + +. +Type +species: + +Ichneumon fornicator +Fabricius, 1781 + +, by subsequent designation ( + +Westwood 1840: 60 + +). + + + + + + +Leptobatus +Gravenhorst, 1829: 432 + + +. +Type +species: + +Leptobatus zeigleri +Gravenhorst, 1829 + +, by subsequent designation ( + +Viereck 1914: 83 + +). + + + + + + +Semnophrys +Förster, 1869: 158 + + +. +Type +species: + +Exetastes notatus +Holmgren, 1860 + +, by subsequent designation ( + +Perkins 1962: 451 + +). + + + + + + +Rhimphalea +Förster, 1869: 202 + + +. +Type +species: + +Rhimphalea brevicorpa +Davis, 1897 + +(= +bioculatus +Cresson, 1872), by subsequent inclusion ( + +Davis 1897: 274 + +). + + + + + +Icyona +Cameron, 1903: 340 + +: +Type +species: + +Icyona rufipes +Cameron, 1903 + +(= + +E. longipes +(Smith, 1878)) + +, by monotypy. + + + + + +Allexetastes +Kokujev, 1904: 106 +. + +Type +species: + +Exetastes +( +Allexetastes +) +komarovi +Kokujev, 1904 + +, by subsequent designation ( +Viereck 1914: 8 +). + + + + + +Rhynchexetastes +Cameron, 1906: 102 + +. +Type +species + +Rhynchexetastes violaceipennis +Cameron, 1906 + +, by monotypy. + + + + + +Tegona +Morley, 1913: 251 + +. +Type +species: + +Tegona rufipes +Morley, 1913 + +(= + +E. longipes +(Smith, 1878)) + +, by monotypy. + + + + + +Pseudexetastes +Meyer, 1927: 308 + +, +Type +species: + +Pseudexetastes diakonovi +Meyer, 1927 + +, by original designation. + + + + + +Diagnosis +(updated from + +Gauld +et al. +2002 + +; +Watanabe 2020 +) + + +Moderate to large body size wasps. Metasoma usually slightly posteriorly compressed. Clypeus in lateral view from weakly convex basally, to almost pyramidal, without a subapical median swelling, in anterior view, not strongly transverse, margin usually fairly evenly sclerotized but thin, slightly concave. Mandibles weakly and evenly tapered apically, lower tooth equal in length, or slightly shorter or slightly longer than upper tooth; both teeth pointed or with the apex of the upper tooth broad and obliquely chisel-shaped ( +Townes 1970 +; +Khalaim & Ruiz-Cancino 2012 +). Occipital carina dorsally complete, its lower part joining hypostomal carina a little above base of mandible. Antenna slender. Scape apically obliquely truncated. Mesosoma short, with the epicnemium sloping slightly backwards ventrally. Pronotum short, anteriorly with a transverse groove before broadly concave hind margin, its upper hind corner bluntly lobed, covering spiracular sclerite. Epomia absent or present as short trace-like ridge. Notauli absent. Mesopleuron with subalar prominence present as a low rounded to sharp promontory. Epicnemium without a distinct vertical tooth-like lamella near lower corner of pronotum. Posterior transverse carina of mesosternum entirely absent. Metanotum with hind rim simple or with a small tooth-like projection posteriorly. Metapleuron with submetapleural carina narrow, only slightly and evenly broadened anteriorly. Metasternum with weak ridges between coxal insertions. Propodeum short and quite steeply declivous.All propodeal carinae (except sometimes the pleural carina) absent. Propodeal spiracle subcircular to slightly oval. Legs slender with tibial spurs long. Hind leg very long and strong, with enlarged coxa. All tarsomeres cylindrical. Tarsal claws simple. Mid tibia without distinct denticles on outer surface. Fore wing with a large kiteshaped areolet. 2m-cu slightly sinuous, with single but long bulla. Usually cu-a opposite or slightly distal to base of Rs and M. Hind wing with distal abscissa of Cu1 joining cu-a close to M. Upper outer corner of subbasal cell almost right-angled, 95–100°. T1 with spiracle in anterior or central part. Glymma vestigial. Sclerotized part of first sternite not reaching spiracle. T2 slightly elongate (l.l–1.4 times as long as broad), with broad shallow thyridium anteriorly. Laterotergites of T2–3 indistinct, laterotergites of T4–5 not distinctly separated. Female hypopygium rather large and completely selerotized. Ovipositor short to moderately long (0.3–1.3 times as long as hind tibia), usually curved downward, compressed basally, its apex usually with a distinct dorsal subapical notch, without teeth on distal end of upper valve; rarely apically elongate tapered with a vestigial apical notch. Male with genital capsule short with a broad shallow notch ventrally. + + + + \ No newline at end of file diff --git a/data/38/72/D1/3872D1F6EA455989B7AA303D0AEA3956.xml b/data/38/72/D1/3872D1F6EA455989B7AA303D0AEA3956.xml new file mode 100644 index 00000000000..60e323eb606 --- /dev/null +++ b/data/38/72/D1/3872D1F6EA455989B7AA303D0AEA3956.xml @@ -0,0 +1,77 @@ + + + +Checklist of national key protected wild plants on the Qinghai-Tibetan Plateau + + + +Author + +Chen, Ronglian +University of Chinese Academy of Sciences, Beijing, China & Qinghai Provincial Key Laboratory of Crop Molecular Breeding, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, China + + + +Author + +Zhang, Faqi +Qinghai Provincial Key Laboratory of Crop Molecular Breeding, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, China + + + +Author + +Chen, Shilong +Qinghai Provincial Key Laboratory of Crop Molecular Breeding, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, China + + + +Author + +Chi, Xiaofeng +Qinghai Provincial Key Laboratory of Crop Molecular Breeding, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, China +xfchi@nwipb.cas.cn + +text + + +Biodiversity Data Journal + + +2023 + +2023-05-16 + + +11 + + +103289 +103289 + + + + +http://dx.doi.org/10.3897/BDJ.11.e103289 + +journal article +http://dx.doi.org/10.3897/BDJ.11.e103289 +1314-2828-11-e103289 +D2D96D0A93125BF2BD8A1911FBE4E783 + + + + +Podocarpus neriifolius D. Don, 1824 + + + +Conservation status +LC + + +Distribution +China, Nepal, India, Bhutan, Myanmar, Vietnam, Laos, Indonesia, Malaysia + + + \ No newline at end of file diff --git a/data/38/72/EA/3872EAA398CB1379749E5B01488987A2.xml b/data/38/72/EA/3872EAA398CB1379749E5B01488987A2.xml new file mode 100644 index 00000000000..439499e1343 --- /dev/null +++ b/data/38/72/EA/3872EAA398CB1379749E5B01488987A2.xml @@ -0,0 +1,82 @@ + + + +A new genus of protorhyssaline wasps in Raritan amber (Hymenoptera, Braconidae) + + + +Author + +Engel, Michael S. + + + +Author + +Thomas, Jennifer C. + + + +Author + +Alqarni, Abdulaziz S. + +text + + +ZooKeys + + +2017 + +711 + + +103 +111 + + + + +http://dx.doi.org/10.3897/zookeys.711.20709 + +journal article +http://dx.doi.org/10.3897/zookeys.711.20709 +1313-2970-711-103 +5E782B9EA87643829F183C620114A212 +5E782B9EA87643829F183C620114A212 + + + + +Subfamily +Protorhyssalinae Basibuyuk et al. + + + +Included genera. + +Archaeorhyssalus +Engel in Engel & Wang (2016), +Diorhyssalus +Engel (2016) +, +Protorhyssalodes +Perrichot et al. (2009) +, +Protorhyssalopsis +Ortega-Blanco et al. (2011) +, +Protorhyssalus +Basibuyuk & Quicke in +Basibuyuk et al. (1999) +, +Rhetinorhyssalites +gen. n. (vide infra), and +Rhetinorhyssalus +Engel (2016) +. + + + + \ No newline at end of file diff --git a/data/38/72/ED/3872EDD40F54E86EA1E262BE20D53935.xml b/data/38/72/ED/3872EDD40F54E86EA1E262BE20D53935.xml new file mode 100644 index 00000000000..8990d0a28e5 --- /dev/null +++ b/data/38/72/ED/3872EDD40F54E86EA1E262BE20D53935.xml @@ -0,0 +1,90 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part M) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +651 +689 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Milium cimicinum +Linnaeus + +, + +Mantissa Plantarum Altera + +: 184. 1771 + + +. + + + +"Habitat in Malabariae et oppidi Johannis plateis. Koenig. 55." RCN: 523. + + + + +Neotype +(Clayton & Renvoize in Polhill, + +Fl. Trop. E. Africa, +Gramineae + +3: 617. 1982): Herb. Linn. No. 83.2 ( +LINN +) + +. + + + + +Current name: + + +Alloteropsis cimicina + +(L.) Stapf + +( +Poaceae +). + + + + \ No newline at end of file diff --git a/data/38/72/FA/3872FAD420708E022FFE01A2A87B9542.xml b/data/38/72/FA/3872FAD420708E022FFE01A2A87B9542.xml new file mode 100644 index 00000000000..155a30913ca --- /dev/null +++ b/data/38/72/FA/3872FAD420708E022FFE01A2A87B9542.xml @@ -0,0 +1,49 @@ + + + +Miscellanea myrmicologiques, II (1905). + + + +Author + +Forel, A. + +text + + +Annales de la Societe Entomologique de Belgique + + +1905 + +49 + + +155 +185 + + + + +http://antbase.org/ants/publications/4001/4001.pdf + +journal article +4001 + + + + +Camponotus lateralis Oliv., v. foveolatus +Mayr. + + + + +- M. le Dr Santschi a decouvert cette espece sur les berges xerothermiques des bords du Rhin, a Stein am Rhein, canton de Schaffouse. Comme cette localite est a deux pas de la frontiere allemande, le +C. lateralis +devra, sans aucun doute, etre ajoute a la faune myrme- cologique de l'Allemagne. Le fait est singulier. + + + + \ No newline at end of file diff --git a/data/38/73/2B/38732B6269BE51E7A6F438A84D1FFC30.xml b/data/38/73/2B/38732B6269BE51E7A6F438A84D1FFC30.xml new file mode 100644 index 00000000000..4fab326ce34 --- /dev/null +++ b/data/38/73/2B/38732B6269BE51E7A6F438A84D1FFC30.xml @@ -0,0 +1,207 @@ + + + +Five new species of Schizoporaceae (Basidiomycota, Hymenochaetales) from East Asia + + + +Author + +Guan, Qian-Xin +https://orcid.org/0000-0002-7072-080X +College of Biodiversity Conservation, Southwest Forestry University, Kunming 650224, China + + + +Author + +Huang, Jing +College of Biodiversity Conservation, Southwest Forestry University, Kunming 650224, China + + + +Author + +Huang, Jian +Yunnan General Administration of Forestry Seeds and Seedlings, Kunming, 650215, China + + + +Author + +Zhao, Chang-Lin +https://orcid.org/0000-0002-8668-1075 +College of Biodiversity Conservation, Southwest Forestry University, Kunming 650224, China & College of Biodiversity Conservation, Southwest Forestry University, Kunming 650224, China & Yunnan Academy of Biodiversity, Southwest Forestry University, Kunming 650224, China +fungichanglinz@163.com + +text + + +MycoKeys + + +2023 + +2023-03-14 + + +96 + + +25 +56 + + + + +http://dx.doi.org/10.3897/mycokeys.96.99327 + +journal article +http://dx.doi.org/10.3897/mycokeys.96.99327 +1314-4049-96-25 +3032456AB3D75FD49DACD31679F781AA + + + + + +Xylodon puerensis C.L. Zhao +sp. nov. + + + + +Figs 12 +, 13 + + + +Type material. + + +Holotype +. + +China. Yunnan Province, Puer, Zhenyuan County, Heping Town, Jinshan Virgin Forest Park, +23°56'21"N +, +101°25'32"E +, altitude 2240 m a.s.l., on fallen angiosperm branch, leg. C.L. Zhao, 21 August 2018, CLZhao 8142 (SWFC). + + + +Etymology. + + +Puerensis + +(Lat.): referring to the locality (Yunnan Province) of the type specimen. + + + +Description. + +Basidiomata annual, resupinate, adnate, coriaceous, without odor or taste when fresh, up to 12 cm long, 5 cm wide, and 200 +µm +thick. Hymenial surface poroid, pores angular or slightly daedaleoid, 3-6 per mm, and cream when fresh, buff on drying. Sterile margin slightly buff, and up to 1 mm wide. + + + +Figure 12. +Basidiomata of + +Xylodon puerensis + +(holotype). Scale bars: 2 cm ( +A +); 1 mm ( +B +). + + + +Hyphal system monomitic, generative hyphae with clamps, colorless, thick-walled, frequently branched, interwoven, 2.5-4.5 +µm +in diameter; IKI-, CB-, tissues unchanged in KOH. + + +Cystidia of four types: (1) paraphysoid cystidia colorless, smooth, 12-20.5 +x +3-5 +µm +; (2) astrocystidia colorless, thin-walled, smooth, 9-11 +x +3.5-5.5 +µm +; (3) capitate cystidia, colorless, thin-walled, smooth, embedded, 22-29.5 +x +6.5-12 +µm +; (4) septocystidia, thin-walled, smooth, with the apical part encrusted, 32-51 +x +3.5-6 +µm +; basidia clavate to subcylindrical, slightly sinuous or distinctly sinuous, with four sterigmata and a basal clamp connection, 14.5-20 +x +5-7 +µm +. + + + +Figure 13. +Microscopic structures of + +Xylodon puerensis + +(holotype) +A +basidiospores +B +basidia and basidioles +C +paraphysoid cystidia +D +astrocystidium +E +capitate cystidia +F +septocystidium cystidia +G +a section of hymenium. Scale bars: 5 +µm +( +A +); 10 +µm +( +B-G +). + + + +Basidiospores ellipsoid to broad ellipsoid, colorless, thin-walled, smooth, with oil drops, IKI-, CB-, (5.5-)6-7 +x +4.5-5.5 +µm +, L = 6.41 +µm +, W = 5.01 +µm +, Q = 1.28 (n = 30/1). + + + +Additional specimen examined + +(paratype). +China. Yunnan Province, Puer, Jingdong County, Taizhong Town, Ailaoshan Ecological Station, +24°29'41"N +, +100°56'32"E +, altitude 1930 m a.s.l., on angiosperm trunk, leg. C.L. Zhao, 24 August 2018, CLZhao 8639 (SWFC). + + + + + \ No newline at end of file diff --git a/data/38/73/43/387343190EF553E98A5C25D03566377D.xml b/data/38/73/43/387343190EF553E98A5C25D03566377D.xml new file mode 100644 index 00000000000..69407596dad --- /dev/null +++ b/data/38/73/43/387343190EF553E98A5C25D03566377D.xml @@ -0,0 +1,217 @@ + + + +Synoptic taxonomy of Cortaderia Stapf (Danthonioideae, Poaceae) + + + +Author + +Testoni, Daniel +Herbario BBB, Departamento de Biologia, Bioquimica y Farmacia, Universidad Nacional del Sur, San Juan 670, CP- 8000 Bahia Blanca, Argentina +daniel.testoni@uns.edu.ar + + + +Author + +Linder, H. Peter +Department of Systematic and Evolutionary Botany, University of Zurich, Zollikerstrasse 107, CH- 8008 Zurich, Switzerland + +text + + +PhytoKeys + + +2017 + +2017-01-11 + + +76 + + +39 +69 + + + + +http://dx.doi.org/10.3897/phytokeys.76.10808 + +journal article +http://dx.doi.org/10.3897/phytokeys.76.10808 +1314-2003-76-39 +FFBD980EFF8A8924FFD5FF9FFF903809 +238999 + + + + +Cortaderia Stapf, Gard. Chron. ser. 3. 22: 378 (1897) +nom. cons. + + + + +Cortaderia +Stapf, Gard. Chron. ser. 3. 22: 378 (1897) nom. cons. Type species: +Cortaderia selloana +(Schult.) Asch. & Graebn. (Syn. Mitteleur. Fl. 2(1): 325. 1900) (Basionym +Arundo selloana +Schult.). + + +Moorea +Lem., Ill. Hort. 2: Misc. 14 (1855) nom. rej., non Rolfe (1890). Type species: +Moorea argentea +(Nees) Lem. ( +Cortaderia selloana +). + + +Lamprothyrsus +Pilg., +Bot. Jahrb. Syst. +37 (Beibl. 85): 58 (1906). Type species: +Lamprothyrsus hieronymi +(Kuntze) Pilg. (Basionym +Triraphis hieronymi +Kuntze). + + + +Description. + +Gynodioecious, dioecious, hermaphrodite or apomictic perennials, ranging from rounded vegetable hedgehogs less than 0.5 m tall to erect 4 m tall tussocks; innovations intravaginal; spreading stolons rare. Leaf sheaths variable: persisting intact, or fragmenting transversely, or decaying into a tangled mass of fibres, or occasionally persisting as burnt-off sheaths; glabrous or more rarely covered in a dense indumentum. Ligule of one or many rows of cilia, to 5 mm long. Leaf blades to 2 m long, tough, expanded, rolled or folded, occasionally pungent, usually persistent but occasionally disarticulating above the ligule, sometimes with an adaxial weft of hairs directly above the ligule; margins sometimes roughly scabrid and cutting. Inflorescences paniculate, sometimes compact but usually plumose, to 1 m long, many-spikeleted, pedicels and pulvini glabrous, scabrid or villous. Spikelets to 30 mm long, with 2-10 florets, disarticulating above the glumes, male spikelets usually less hairy than female spikelets and glabrous in the Selloana group; glumes glabrous, often papery or membranous, 4-30 mm long, usually 1-veined and rarely with no veins, upper and lower glumes similar. Lemmas (Fig. +1 +) 3-7 nerved, mostly with the central three nerves continuing into a more or less twisted awn; the lateral nerves sometimes terminating in lateral bristles, the lemmas often continuing up the awns, consequently with the bristles apparently borne on the awn, in + +Cortaderia selloana + +the lemma continues to the tip of the awn and so obscures the awn; lemmas usually long-villous on the back, rarely glabrous. Palea membranous, linear, often longer than the lemma, keeled, sometimes variously villous on the back. Lodicules two. Anthers three, fertile or sterile, to 3.5 mm long. Ovary stalked, styles two. Caryopses 1.5-3.5 mm long, variable in shape, glabrous, embryo mark from +1/4 +to more than +1/2 +length of caryopsis, hilum linear, from +1/4 +to +3/4 +caryopsis length. + + + +Figure 1. +Lemmas of selected species of + +Cortaderia + +. +A + +Cortaderia selloana + +, + +Juergens +40 + +(B) +B + +Cortaderia araucana + +, +Borchers +s.n. (US) +C + +Cortaderia speciosa + +, +P.M. Peterson 12766 +(US) +D + +Cortaderia vaginata + +, +L.B. Smith, P.R. Reitz & R. Klein 7761 +(B) +E + +Cortaderia egmontiana + +, +P.M. Peterson, R.J. Soreng & N. Refulio-Rodriguez 17508 +(US) +F + +Cortaderia modesta + +, +A. Chase 8288 +(US) +G + +Cortaderia hieronymi + +, +A. Burkart et al. 30395 +(P) - note that awn and setae are much longer than illustrated +H + +Cortaderia nitida + +, +S. Laegaard 52786 +(K) +I + +Cortaderia sericantha + +, +E. Asplund 17175 +(B) +J + +Cortaderia bifida + +, +D.N. Smith & J. Cabanillas 7167 +(US) +K + +Cortaderia hapalotricha + +, +J.C. Solomon & R. Chevalier 16620 +L + +Cortaderia columbiana + +, +J.P. Schulz 318 +(US). All at same magnification. + + + + +Leaf anatomy. + +Leaf in transverse section sclerophyllous, leaves varying from expanded to setaceous, margins not thickened but with a sclerenchyma cap. Adaxial furrows vary from deep and cleft-like to absent; abaxial ribs sometimes present. Vascular bundles differentiated into two, rarely three, orders; primary vascular bundles 6-30, symmetrically distributed in the two leaf sections; either ad- or abaxially or centrally positioned, circular or elliptical, sometimes with sclerosed phloem; outer bundle sheath cells always distinct from the chlorenchyma and sometimes lignified, entire or interrupted by bundle sheath; adaxial sclerenchyma as narrow girders, as +trapezoidal +girders, as T-shaped girders or inversely anchor-shaped girders; abaxial sclerenchyma as small strands, as narrow girders, as wide girders, as trapezoidal girders, or as massive linked girders forming a continuous subepidermal layer; tertiary vascular bundles 1-several between the primary vascular bundles, adaxial sclerenchyma as small strands, as narrow girders, as trapezoid girders narrowing towards vascular bundles, as T-shaped girders or inversely anchor-shaped girders; abaxial sclerenchyma absent, as small strands, as narrow girders, as broad girders, as trapezoidal girders or as massive linked girders forming a continuous subepidermal layer. Mesophyll of small, angular isodiametric chlorenchyma cells with small air spaces; mesophyll islands of colourless cells usually absent, sometimes with colourless collenchyma cells connecting the adaxial and abaxial furrows and so partitioning the chlorenchyma. Abaxial subepidermal layer sometimes with collenchymatous or non-chlorophyllous cells in 1-several layers only along the margins, or flanking the midrib, and sometimes with this layer extending over the whole width of the leaf. Abaxial epidermal zonation present or absent; microhairs or macrohairs absent; silica bodies absent, or tall and narrow, or round and single. Adaxial epidermis sometimes with papillae, prickle-hairs, and microhairs. + + + +Distribution and ecology. + +Widespread in South America, from Tierra del Fuego (Argentina) to Venezuela, from Brazil to Peru, from sea level to the +Paramo +. + + + + \ No newline at end of file diff --git a/data/38/73/E0/3873E00488FA926B058F75AB28B4839B.xml b/data/38/73/E0/3873E00488FA926B058F75AB28B4839B.xml new file mode 100644 index 00000000000..34d11b17e1b --- /dev/null +++ b/data/38/73/E0/3873E00488FA926B058F75AB28B4839B.xml @@ -0,0 +1,77 @@ + + + +Cyanobacteria of Greece: an annotated checklist + + + +Author + +Gkelis, Spyros + + + +Author + +Ourailidis, Iordanis + + + +Author + +Panou, Manthos + + + +Author + +Pappas, Nikos + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +10084 +10084 + + + + +http://dx.doi.org/10.3897/BDJ.4.e10084 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e10084 +1314-2828-4-10084 + + + + + +Microcystis novacekii ( +Komarek +) +Compere +, 1974 + + + + + +Microcystis novacekii + + + +Notes + +Vardaka et al. 2000 + + + + \ No newline at end of file diff --git a/data/38/74/08/387408A18F727B8C56D133EEF70EE8EE.xml b/data/38/74/08/387408A18F727B8C56D133EEF70EE8EE.xml new file mode 100644 index 00000000000..2ebb9d0b4d8 --- /dev/null +++ b/data/38/74/08/387408A18F727B8C56D133EEF70EE8EE.xml @@ -0,0 +1,52 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828--9042 + + + + +Eupalamus wesmaeli (Thomson, 1886) + + + + +Ichneumon wesmaeli +Thomson, 1886 + + + +Distribution +England + + + \ No newline at end of file diff --git a/data/38/74/37/387437134C4D5E358034A0D09ED16019.xml b/data/38/74/37/387437134C4D5E358034A0D09ED16019.xml new file mode 100644 index 00000000000..5fd97111a19 --- /dev/null +++ b/data/38/74/37/387437134C4D5E358034A0D09ED16019.xml @@ -0,0 +1,82 @@ + + + +Hornmilben (Oribatida) [pages 261 to 322] + + + +Author + +Weigmann, G. + + + +Author + +Miko, L. + +text + + +2006 +Goecke & Evers + +Keltern + + + +Hornmilben (Oribatida) [Dahl, Tierwelt Deutschlands, Teil 76] + + + +261 +322 + + + + +http://www.goeckeevers.de/verlag/dahl.html + +book chapter +Weigmann2006pp261to322 + + + + +Suctobelbella subtrigona +(Oudemans, 1916) [165a-d] + + + + +Syn., Tax.: +Xenillus s. +: Oudemans, 1916. +Suctobelbella s. +: Moritz 1971 (B). + + + + +- +Suctobelba intermedia +Willmann, 1939: Forsslund 1941; Strenzke 1951c (B). + + + + +Oekologie +: Feuchte bis trockene +Waldboeden +. + + + + +Verbreitung: Holarktis, +Suedamerika +. + + + + \ No newline at end of file diff --git a/data/38/74/5B/38745B7FFFA0FF90FF4ECE64FF3CC2DB.xml b/data/38/74/5B/38745B7FFFA0FF90FF4ECE64FF3CC2DB.xml new file mode 100644 index 00000000000..b92f5484c20 --- /dev/null +++ b/data/38/74/5B/38745B7FFFA0FF90FF4ECE64FF3CC2DB.xml @@ -0,0 +1,130 @@ + + + +Identification of Ceriodaphnia Dana, 1853 (Crustacea: Cladocera) taxa from European Russia based on ephippial morphology + + + +Author + +Kotov, Alexey A. + + + +Author + +Ibragimova, Aisylu G. + + + +Author + +Neretina, Anna N. + +text + + +Zootaxa + + +2018 + +2018-12-04 + + +4527 + + +1 + + +105 +123 + + + +journal article +27862 +10.11646/zootaxa.4527.1.9 +021796c0-cde1-4dfd-a83a-3b1c83ce466b +1175-5326 +2612039 +C9D04EAA-61CD-4706-9B54-026C5A7FD98F + + + + + + +Ceriodaphnia + +pulchella +Sars, 1862 + + + + + + + +( +Figs. 9–10 +) + + +Length about +0.35 mm +, width about 0.7 of length. In lateral view, ephippium semicircular; dorsal margin straight; ventral margin regularly curved from postero-ventral to antero-ventral angle ( +Figs. 9A +, +10 +A–C). Paired latero-dorsal ridges absent ( +Figs. 9 +B–C). A depression along dorsum separates two halves of ephippium well-visible; sculpture of dorsal plate without any wrinkles, with numerous low spots covered by minute tubercles ( +Fig. 9D +). Egg locule very slightly extends laterally, without any wrinkles, in general smooth ( +Fig. 9C +), but bearing minute tubercles sometimes organized into spots ( +Fig. 9E +), probably these spots make locule surface non-transparent under light microscope ( +Figs. 10 +D–D). Space between egg locule and dorsal margin with same sculpture. The rest of ephippium with obscure (under SEM) polygonal reticulation ( +Fig. 9F +) – external sign of air-spaces which are well-visible under light microscope ( +Figs. 10 +D–F); lines of reticulation with especially minute tubercles. Ephippium has a very narrow ventral rim with obscure reticulation, lacking any tubercles ( +Figs. 9F +, +10F +). + + + +FIGURE 9. +Ceriodaphnia + +pulchella +Sars, 1862 + +, ephippial female from a pond in stadium of AZLK factory near Metro Station "Textilshchiky", Moscow city. A, lateral view of female. B, dorsal view of ephippium. C, antero-lateral view. D, fragment of ephippium dorsal portion, lateral view. E, sculpture of its central portion. F, postero-ventral portion of ephippium. Scale bars: 0.1 mm for A–C; 0.01 mm for D–F. + + + + +FIGURE 10. +Ceriodaphnia + +pulchella +Sars, 1862 + +, ephippial female from a pond in stadium of AZLK factory near Metro Station "Textilshchiky", Moscow city. A–B, ephippial female with a single egg in ephippium, lateral view. C–D, opened ephippium. E–F, its dorsal and ventral portion. Scale bars: 0.1 mm. + + + +Note that in our material the ephippia were unusually small as compared to previous descriptions ( +Jaksch 1992 +). + + + + \ No newline at end of file diff --git a/data/38/74/5B/38745B7FFFA2FF95FF4ECCEDFD16C4C7.xml b/data/38/74/5B/38745B7FFFA2FF95FF4ECCEDFD16C4C7.xml new file mode 100644 index 00000000000..65ecfef4531 --- /dev/null +++ b/data/38/74/5B/38745B7FFFA2FF95FF4ECCEDFD16C4C7.xml @@ -0,0 +1,101 @@ + + + +Identification of Ceriodaphnia Dana, 1853 (Crustacea: Cladocera) taxa from European Russia based on ephippial morphology + + + +Author + +Kotov, Alexey A. + + + +Author + +Ibragimova, Aisylu G. + + + +Author + +Neretina, Anna N. + +text + + +Zootaxa + + +2018 + +2018-12-04 + + +4527 + + +1 + + +105 +123 + + + +journal article +27862 +10.11646/zootaxa.4527.1.9 +021796c0-cde1-4dfd-a83a-3b1c83ce466b +1175-5326 +2612039 +C9D04EAA-61CD-4706-9B54-026C5A7FD98F + + + + + + +Ceriodaphnia + +quadrangula +(O.F. Müller, 1785) + + + + + + + +( +Figs. 7–8 +) + + +Length about +0.35–0.4 mm +, width about 0.6–0.65 of length. In lateral view, ephippium semicircular; dorsal margin slightly convex to almost straight; ventral margin regularly curved from postero-ventral to antero-ventral angle ( +Figs. 7 +A–B, 8A–D). Paired latero-dorsal ridges absent ( +Figs. 7 +S–C). A distinct depression along dorsum separates two halves of ephippium and, respectively, two halves of dorsal plate with sculpture of relatively thick small columns with branched tips ( +Figs. 7 +D–E); no any wrinkles or low projections are detected, no air spaces in this region. Egg locule somewhat extends laterally ( +Fig. 7B +); surface of locule with columns bearing branched tips as in the region of dorsal plate ( +Figs. 7 +E–F). The rest of ephippium surface covered by same columns, but towards the margins they diminishing in size, and finally they are transformed into circles of small tubercles ( +Fig. 7H +). Airspaces expressed in ventral portion of ephippium well-visible under light microscope ( +Figs. 8 +C–F), but no their signs visible under SEM, excluding most ventral portion, where they are slightly elevated above the general surface, just each air space bears the circle of small tubercles described above ( +Fig. 7H +). Ventral rim of ephippium lacking air spaces, without reticulation ( +Figs. 7H +, +8F +). + + + + \ No newline at end of file diff --git a/data/38/74/5B/38745B7FFFA7FF90FF4ECB73FBDCC720.xml b/data/38/74/5B/38745B7FFFA7FF90FF4ECB73FBDCC720.xml new file mode 100644 index 00000000000..53173d7f8d0 --- /dev/null +++ b/data/38/74/5B/38745B7FFFA7FF90FF4ECB73FBDCC720.xml @@ -0,0 +1,101 @@ + + + +Identification of Ceriodaphnia Dana, 1853 (Crustacea: Cladocera) taxa from European Russia based on ephippial morphology + + + +Author + +Kotov, Alexey A. + + + +Author + +Ibragimova, Aisylu G. + + + +Author + +Neretina, Anna N. + +text + + +Zootaxa + + +2018 + +2018-12-04 + + +4527 + + +1 + + +105 +123 + + + +journal article +27862 +10.11646/zootaxa.4527.1.9 +021796c0-cde1-4dfd-a83a-3b1c83ce466b +1175-5326 +2612039 +C9D04EAA-61CD-4706-9B54-026C5A7FD98F + + + + + + +Ceriodaphnia + +reticulata +(Jurine, 1820) + + + + + + + +( +Figs. 11–12 +) + + +Length about +0.6 mm +, width about 0.6 of length. In lateral view, ephippium almost semicircular; dorsal margin straight; ventral margin regularly curved from postero-ventral angle to antero-ventral portion which is almost perpendicular to dorsal margin ( +Figs. 11 +A–C, 12A–D). Paired latero-dorsal ridges absent ( +Fig. 11B +). A depression along dorsum separating two halves of ephippium well-visible ( +Fig. 11B +); sculpture of dorsal plate without any wrinkles, without any spots, covered by thin, minute filiform projections ( +Fig. 11D +). Egg locule very slightly extends laterally, without any wrinkles; in general smooth, but bearing minute tubercles ( +Figs. 11 +E–F) too small to make the surface non-transparent ( +Figs. 12 +D–F). Space between egg locule and dorsal margin with same sculpture. The rest of ephippium with obscure (under SEM) polygonal reticulation ( +Fig. 11E +) – external sign of air-spaces which are well visible under light microscope ( +Figs. 12 +C–D), and sculpture as in egg locule. Ephippium with narrow ventral rim and obscure reticulation, lacking any tubercles ( +Figs. 11C +, +12F +). + + + + \ No newline at end of file diff --git a/data/38/74/5B/38745B7FFFABFF99FF4ECF7DFA7FC44B.xml b/data/38/74/5B/38745B7FFFABFF99FF4ECF7DFA7FC44B.xml new file mode 100644 index 00000000000..6884648224d --- /dev/null +++ b/data/38/74/5B/38745B7FFFABFF99FF4ECF7DFA7FC44B.xml @@ -0,0 +1,105 @@ + + + +Identification of Ceriodaphnia Dana, 1853 (Crustacea: Cladocera) taxa from European Russia based on ephippial morphology + + + +Author + +Kotov, Alexey A. + + + +Author + +Ibragimova, Aisylu G. + + + +Author + +Neretina, Anna N. + +text + + +Zootaxa + + +2018 + +2018-12-04 + + +4527 + + +1 + + +105 +123 + + + +journal article +27862 +10.11646/zootaxa.4527.1.9 +021796c0-cde1-4dfd-a83a-3b1c83ce466b +1175-5326 +2612039 +C9D04EAA-61CD-4706-9B54-026C5A7FD98F + + + + + + +Ceriodaphnia + +laticaudata +P.E. Müller, 1867 + + + + + + + +( +Figs. 3–4 +) + + +Length about +0.4–0.45 mm +, width about 0.66–0.7 of length. In lateral view, ephippium asymmetrical, narrowing posteriorly; dorsal margin straight; ventral margin regularly curved from postero-ventral to anterior margin which is almost perpendicular to dorsal margin ( +Figs. 3A, E +, +4 +A–D). Paired latero-dorsal ridges absent ( +Figs. 3 +B–C). A depression along dorsum separating two halves of ephippium well-visible; sculpture of dorsal plate as a few wavy longitudinal wrinkles and numerous spots of minute tubercles ( +Figs. 3D, F +). Egg locule visibly extending laterally ( +Figs. 3 +B–C), without any wrinkles, but with numerous, densely located semicircular projections ( +Figs. 3 +E–H) well-visible also under optical microscope ( +Fig. 4E +); a circular row of minute tubercles on each semicircular projection ( +Fig. 3G +). Space between egg locule and dorsal margin with low, flattened projections (not associated with any air-spaces), bearing minute tubercles ( +Fig. 3F +). Rest of ephippium surface covered by low, densely located flattened domes ( +Fig. 3H +) – external signs of air-spaces which are well-visible under light microscope ( +Figs. 4 +C– F), each dome with a spot of minute tubercles. Ephippium with narrow ventral rim lacking any sculpture ( +Fig. 3E +). + + + + \ No newline at end of file diff --git a/data/38/74/5B/38745B7FFFABFF9CFF4ECAFBFEDEC52C.xml b/data/38/74/5B/38745B7FFFABFF9CFF4ECAFBFEDEC52C.xml new file mode 100644 index 00000000000..673f080af05 --- /dev/null +++ b/data/38/74/5B/38745B7FFFABFF9CFF4ECAFBFEDEC52C.xml @@ -0,0 +1,109 @@ + + + +Identification of Ceriodaphnia Dana, 1853 (Crustacea: Cladocera) taxa from European Russia based on ephippial morphology + + + +Author + +Kotov, Alexey A. + + + +Author + +Ibragimova, Aisylu G. + + + +Author + +Neretina, Anna N. + +text + + +Zootaxa + + +2018 + +2018-12-04 + + +4527 + + +1 + + +105 +123 + + + +journal article +27862 +10.11646/zootaxa.4527.1.9 +021796c0-cde1-4dfd-a83a-3b1c83ce466b +1175-5326 +2612039 +C9D04EAA-61CD-4706-9B54-026C5A7FD98F + + + + + + +Ceriodaphnia + +megops +Sars, 1862 + + + + + + + +( +Figs. 1–2 +) + + +Length about +0.5–0.55 mm +, width about 0.7 of length. In lateral view, ephippium almost semicircular, somewhat asymmetrical, stronger narrowing posteriorly; dorsal margin almost straight; ventral margin regularly curved from postero-ventral to antero-ventral angle ( +Figs. 1A +, +2 +A–D). Paired latero-dorsal ridges strongly expressed ( +Figs. 1 +B– D), extend above dorsal margin as seen laterally ( +Figs. 1A +, +2 +A–D), their dorsal margin slightly and regularly convex. A distinct depression along dorsum separating two halves of ephippium and, respectively, two halves of dorsal plate; sculpture of dorsal plate consisting of a series of longitudinal wrinkles ( +Figs. 1 +D–E). Sculpture on latero-dorsal ridges low, consisting of small semicircular projections ( +Figs. 1 +D–F); the external signs of roundedhexagonal air-spaces well-visible under light microscope ( +Fig. 2E +). Egg locule smooth, only somewhat extending laterally, with poorly expressed vertical wrinkles ( +Fig. 1B +, F–G); under optical microscope, surface of locule relatively smooth, with small irregularities ( +Fig. 2E +). Rest of ephippium surface covered by low, dense, flattened domes ( +Figs. 1 +G–H); the external signs of air-spaces well-visible under light microscope ( +Figs. 2D, F +). Such air spaces absent in the locule region. Ventral rim of ephippium lacking air spaces, with obscure polygonal reticulation ( +Figs. 1H +, +2F +). + + + + \ No newline at end of file diff --git a/data/38/74/5B/38745B7FFFACFF95FF4ECFA5FB64C6A5.xml b/data/38/74/5B/38745B7FFFACFF95FF4ECFA5FB64C6A5.xml new file mode 100644 index 00000000000..5d59870f750 --- /dev/null +++ b/data/38/74/5B/38745B7FFFACFF95FF4ECFA5FB64C6A5.xml @@ -0,0 +1,103 @@ + + + +Identification of Ceriodaphnia Dana, 1853 (Crustacea: Cladocera) taxa from European Russia based on ephippial morphology + + + +Author + +Kotov, Alexey A. + + + +Author + +Ibragimova, Aisylu G. + + + +Author + +Neretina, Anna N. + +text + + +Zootaxa + + +2018 + +2018-12-04 + + +4527 + + +1 + + +105 +123 + + + +journal article +27862 +10.11646/zootaxa.4527.1.9 +021796c0-cde1-4dfd-a83a-3b1c83ce466b +1175-5326 +2612039 +C9D04EAA-61CD-4706-9B54-026C5A7FD98F + + + + + + +Ceriodaphnia + +rotunda +(Straus, 1820) +sensu +Sars, 1862 + + + + + + + +( +Figs. 5–6 +) + + +Length about +0.5 mm +, width about 0.75 of length. In lateral view, ephippium semicircular; dorsal margin very slightly convex; ventral margin regularly curved from postero-ventral to anterior margin ( +Figs. 5A +, +6 +A–B, D). Paired latero-dorsal ridges absent. A depression along dorsum separating two halves of ephippium indiscernible; sculpture of dorsal plate consisting of very thin longitudinal wrinkles and numerous minute columns, not organized into spots ( +Figs. 5 +B–C). Egg locule visibly extends laterally, without any wrinkles, but with numerous, densely located semicircular projections ( +Figs. 5B, D +) well visible also under optical microscope ( +Fig. 6C +); a patch of minute columns on each semicircular projection. Space between egg locule and dorsal margin with low, flattened projections (not associated with any air-spaces) bearing patches of minute columns ( +Fig. 5B +). The rest of ephippium surface covered by low, densely located flattened domes ( +Figs. 5 +F–F, 6C) — external signs of air-spaces which are well-visible under light microscope, each dome with a spot of minute tubercles. Ephippium has a very narrow ventral rim without any sculpture ( +Fig. 5F +). In general, minute tubercles (i.e. represented by minute columns) are better developed in all portions of ephippium as compared to + +C. laticaudata + +. + + + + \ No newline at end of file diff --git a/data/38/74/5E/38745E26D0F6C3A9E9833EFD31CEDED7.xml b/data/38/74/5E/38745E26D0F6C3A9E9833EFD31CEDED7.xml new file mode 100644 index 00000000000..8b0a33d7d46 --- /dev/null +++ b/data/38/74/5E/38745E26D0F6C3A9E9833EFD31CEDED7.xml @@ -0,0 +1,46 @@ + + + +Pseudancistrus sidereus, a new species from southern Venezuela (Siluriformes: Loricariidae) with a redescription of Pseudancistrus. + + + +Author + +Jonathan W. Armbruster + +text + + +Zootaxa + + +2004 + +628 + + +1 +15 + + + + +http://www.zoobank.org/urn:lsid:zoobank.org:pub:C8D199F9-0677-41B1-ACD1-8A685EE26AE2 + +journal article +z00628p001 +C8D199F9-0677-41B1-ACD1-8A685EE26AE2 + + + + +P. orinoco +: + + + +ANSP 165824, 1, 78.1; MCNG 17525, 2, 64.6-94.4; MCNG 18410, 1, 52.0-62.9; MCNG 20205, 3, 29.0-33.6; MCNG 29524, 2, 62.7-82.6; MCNG 30407, 2, 45.5-58.4. + + + \ No newline at end of file diff --git a/data/38/74/D3/3874D31CED5F521260CCD7257DB1BE43.xml b/data/38/74/D3/3874D31CED5F521260CCD7257DB1BE43.xml new file mode 100644 index 00000000000..b5dad661373 --- /dev/null +++ b/data/38/74/D3/3874D31CED5F521260CCD7257DB1BE43.xml @@ -0,0 +1,428 @@ + + + +Flora der Schweiz und angrenzender Gebiete. Band 2. Nymphaceae bis Primulaceae (2 nd edition) (p. 956): Rosaceae + + + +Author + +Hess, Hans Ernst + + + +Author + +Landolt, Elias + + + +Author + +Hirzel, Rosmarie + +text + +1976 +Birkhaeuser Verlag + + +https://doi.org/10.5281/zenodo.292251 + +book +292251 +10.5281/zenodo.292251 +3-7643-0527-4 + + + +<subSubSection id="0E8491AC6C5CD4FB5347619ECC19D704" pageId="null" pageNumber="476" type="nomenclature"> +<paragraph id="A666406EBDC1F77738C78CD8B181A3C4" pageId="null" pageNumber="476"> +<taxonomicName id="0F9A21D8EE5F01AAB5227A13FD80B7FE" authority="L." class="Magnoliopsida" family="Rosaceae" genus="Sorbus" kingdom="Plantae" order="Rosales" pageId="null" pageNumber="476" phylum="Tracheophyta" rank="genus"> +<pageBreakToken id="6638118C0B29FCFA4301096393462EF6" pageId="null" pageNumber="476" start="start"> +<normalizedToken id="FD7A48F68B980B33DA99307C733E4A51" originalValue="Sórbus" pageId="null" pageNumber="476">Sorbus</normalizedToken> +</pageBreakToken> +<authorityName id="85D714CE3B04580C92B9392E6D485BB9" pageId="null" pageNumber="476">L.</authorityName> +</taxonomicName> +</paragraph> +</subSubSection> +<subSubSection id="A75F84BCBC90752E35585BCBA60E0E63" pageId="null" pageNumber="476" type="vernacular_names"> +<paragraph id="96A68C2CEF1651A50AB63CA7D29A1E90" pageId="null" pageNumber="476">Eberesche</paragraph> +</subSubSection> + + + +Sommergruene +Straeucher +oder +Baeume +, ohne Dornen. + +Blaetter +gezaehnt +, geteilt oder gefiedert + +(mit Endteilblatt), in der Knospenlage gefaltet. + +Bluetenstaende +sind +reichbluetige +, doldenartige Rispen. + +Kelch 1fach; +Kelchblaetter +5, 3eckig, an der reifen Frucht aufgerichtet oder +zurueckgebogen +oder vor der Fruchtreife abfallend. +Kronblaetter +5, rundlich bis oval, +weiss +, gelblich, seltener rot, oberseits +ueber +dem Grunde oft wollig behaart. +Staubblaetter +15-25. +Fruchtblaetter +2-5, aus pergamentartigem, +zaehem +Gewebe, bis zur Mitte miteinander verwachsen, 2samig; Griffel 2-5, frei oder im untern Teil verwachsen. +Scheinfrucht kugelig +oder +eifoermig +, im +Durchmesser 0,5-1 cm, rot, gelb oder braun; +Fruchtfleisch mehlig. + + +Die Gattung + +Sorbus + +ist auf der + +noerdlichen +Hemisphaere +verbreitet. + +In der Monographie der Gattung + +Sorbus +von Hedlund (1901) + +sind 55 Arten +erwaehnt +, heute werden + +ungefaehr +100 Arten + +angegeben. +Die Struktur der Gattung ist wesentlich durch die zytologischen Arbeiten von +Liljefors (1953 1955, s. auch die dort zitierte Literatur) +aufgeklaert +worden: + +S. +Aria +, +S. aucuparia +, S. +Chamaemespilus + +und +S. torminalis sind diploid +( +2n += +34 +) +und normal sexuell. Alle diploiden Arten +( +soweit untersucht +) +und nur diese sind normal sexuell. +Neben den normal sexuellen gibt es +2 Gruppen von apomiktischen Arten: +a) + +Intermediaere +Arten + +zwischen + +S. +Aria + +und einer andern der oben +erwaehnten +Arten; es handelt sich dabei um +polyploide Bastarde +, die durch kleine, aber fixierte Merkmale charakterisiert sind, b) + +Arten, die S. +Aria +oder S. +Chamaemespilus +aehnlich +sehen; + +dies sind +triploide +(2n = 51) oder +tetraploide +(2n = 68) + +S. +Aria + +oder + +triploide S. +Chamaemespilus +. + +Alle apomiktischen Sippen zeigen + +auffallende +Stoerungen +in der Pollenmeiose + +, so +dass +die +Pollenkoerner +zum +grossen +Teil +verkuemmert +sind; der Embryosack entwickelt sich aus somatischen, seltener aus generativen Zellen (keine Chromosomenreduktion). - +Aus Kreuzungen zwischen diploiden Arten entstehen diploide Bastarde, die normal sexuell sind; +die meiotischen Teilungen im Pollen sind + +wenig +gestoert + +und die +Fertilitaet +ist gut. Aus diesen zytologischen Tatsachen folgen +fuer +die Systematik +aehnliche +Schwierigkeiten wie in der Gattung + +Rubus: Zwischen +sexuellen Hauptarten entstehen echte, normal sexuelle Bastarde, zudem gibt es im gleichen Variationsbereich der Merkmale konstante, apomiktische Sippen, ebenfalls aus Bastardierungen hervorgegangen; weiter haben sich durch Autopolyploidie und nachherige Apomixis sexuelle Hauptarten ohne Bastardierung weiter differenziert. + +Die zytologischen Untersuchungen wurden von Liljefors (1953 von Liljefors (1955) zur Hauptsache an +skandinavischem Material +gemacht; sie haben wahrscheinlich auch +fuer +unser Gebiet +Gueltigkeit +. + + +Die +in der Tschechoslowakei vorkommenden Arten (alle unsere Arten kommen auch dort vor) sind von Kovanda (1961) auf + +Unterschiede an +Blueten +und +Fruechten + +untersucht worden ( +Schluessel +, +ausfuehrliche +Beschreibungen) Die Vielgestaltigkeit der + +Sorbus + +arten in Ungarn wird von +Karpati +(1949 von +Karpati +(1950) dargestellt. Aus Osteuropa beschreibt +Karpati +(1964) zahlreiche konstante apomiktische Sippen, die aus Kreuzungen zwischen + +S. +Aria + +und +S. torminalis +entstanden sind. Aus Bayern und +Thueringen +werden die vorhandenen Arten und Bastarde von +Duell +(1961) beschrieben, wobei aus apomiktischen Sippen neue Arten aufgestellt werden. Sammelreferat +ueber +die Taxonomie der +europaeischen +Sorbu +sarten von +Karpati +(1965). + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+1. +Blaetter +gefiedert, mit Endteilblatt. +
+2. Rand der +Teilblaetter +beiderseits bis fast zum Grunde scharf +gezaehnt +( +hoechstens +⅕ der +Laenge +ohne +Zaehne +); Griffel 2-4 + + +S. aucuparia + +(Nr. 1) +
+2*. Rand der +Teilblaetter +wenigstens auf der einen Seite nur in der obern +Haelfte +oder in den obern ⅔ mit +Zaehnen +; Griffel 5 + + +S. domestica + +(Nr. 2) +
+1*. +Blaetter +nicht gefiedert. +
+3. +Blaetter +unterseits mit 3-5 auffallend hervortretenden Seitennerven, jederseits mit 3-4 +allmaehlich +zugespitzten Abschnitten, unterstes Abschnittpaar am +groessten +, +ungefaehr +senkrecht zum Blattmittelnerv abstehend, obere Abschnitte +vorwaerts +gerichtet + +S. torminalis +(Nr. 3) +
+3*. +Blaetter +unterseits mit 6-14 auffallend hervortretenden Seitennerven. +
+4. Alle +Blaetter +stets beiderseits +gruen +, Rand 1fach +gezaehnt +(einzelne +Blaetter +doppelt +gezaehnt +), +Zaehne +etwa 1 mm lang, spitz + + +S. +Chamaemespilus + +(Nr. 4) +
+4*. Alle +Blaetter +unterseits grau bis +weiss +, dicht filzig behaart, meist doppelt +gezaehnt +. +
+5. +Zaehne +1. Ordnung in der Mitte des Randes nicht +ueber +3 mm lang, mit deutlicher Spitze + + +S. +Aria + +(Nr. 5) +
+5*. +Zaehne +1. Ordnung in der Mitte des Randes 4-6 mm lang, im +Umriss +breit abgerundet + + +S. Mougeotii + +(Nr. 6) +
+
+ + + +<normalizedToken id="B53DCF8182D3D79B57754401FC30DE1D" originalValue="Schlüssel" pageId="null" pageNumber="473">Schluessel</normalizedToken> +zur Gattung +<taxonomicName id="B8EA8420E2D971272BB3B1F8C72D4F6C" class="Magnoliopsida" family="Rosaceae" genus="Sorbus" kingdom="Plantae" order="Rosales" pageId="null" pageNumber="473" phylum="Tracheophyta" rank="genus">Sorbus</taxonomicName> + + + +
+
+
\ No newline at end of file diff --git a/data/38/74/D6/3874D6B9C3EEBF43B526DCA8143F1F43.xml b/data/38/74/D6/3874D6B9C3EEBF43B526DCA8143F1F43.xml new file mode 100644 index 00000000000..e91dd3378e9 --- /dev/null +++ b/data/38/74/D6/3874D6B9C3EEBF43B526DCA8143F1F43.xml @@ -0,0 +1,218 @@ + + + +A review of the Madagascan pelican spiders of the genera Eriauchenius O. Pickard-Cambridge, 1881 and Madagascarchaea gen. n. (Araneae, Archaeidae) + + + +Author + +Wood, Hannah M. + + + +Author + +Scharff, Nikolaj + +text + + +ZooKeys + + +2017 + +727 + + +1 +96 + + + + +http://dx.doi.org/10.3897/zookeys.727.20222 + +journal article +http://dx.doi.org/10.3897/zookeys.727.20222 +1313-2970-727-1 +12B663F7190040788E1EEF8BAC4DF81B +12B663F7190040788E1EEF8BAC4DF81B + + + + +Eriauchenius rafohy +sp. n. +Figs 5, 30 + + + +Type material. + +Male holotype: Madagascar, Antananarivo, +Reserve +Speciale +d'Ambohitantely +, +Foret +d'Ambohitantely +, 20.9 km 72° NE Ankazobe, +18°13'31"S +, +47°17'13"E +, 1410 m., 17-22 Apr 2001, montane rainforest, general collecting night, J.J. Rafanomezantsoa et al. (deposited in CAS; CASENT9006503). + + + +Other material examined. + +MADAGASCAR: 3F, together with the holotype (CASENT 9006503); Paratype female,1M, 1 hatched eggcase, Antananarivo, +Reserve +Speciale +d'Ambohitantely +, +Foret +d'Ambohitantely +, 20.9 km 72° NE Ankazobe, +18°13'30.3"S +, +47°16'44"E +, 1574 m., 19 Mar 2003, primary montane rainforest, Ldd fallen logs/litter (among fallen logs and litter), D. Andriamalala, D. Silva, et al. (CASENT 9015039); 1M,1Juv, Antananarivo, +Reserve +Speciale +d'Ambohitantely +, +Foret +d'Ambohitantely +, 20.9 km 72° NE Ankazobe, +18°13'30.3"S +, +47°16'44"E +, 1574 m, 20 Mar 2003, primary montane rainforest, Ludd/raking, D. Andriamalala, D. Silva, et al. (CASENT9015019); 3M, 3F,>70Juvs, Antananarivo, 3 km 41° NE Andranomay, 11.5 km 147° SSE Anjozorobe, +18°28'24"S +, +47°57'36"E +, 1300 m., 5-13 Dec 2000, montane rainforest, general collecting, Fisher, Griswold et al. (CASENT9004087, CASENT9004076); 2F,6Juv, Antananarivo, 3 km 41° NE Andranomay, 11.5 km 147° SSE Anjozorobe, +18°28'24"S +, +47°57'36"E +, 1300 m., 5-13 Dec 2000, montane rainforest, beating low vegetation, Fisher, Griswold et al. (CASENT9003844); 1F,8Juv, Antananarivo, 3 km 41° NE Andranomay, 11.5 km 147° SSE Anjozorobe, +18°28'24"S +, +47°57'36"E +, 1300 m., 5-13 Dec 2000, montane rainforest, beating and sweeping, Fisher, Griswold et al. (CASENT9004010); 1F,1Juv, Antananarivo, 3 km 41° NE Andranomay, 11.5 km 147° SSE Anjozorobe, +18°28'24"S +, +47°57'36"E +, 1300 m., 5-13 Dec 2000, montane rainforest, cryptic searching, Fisher, Griswold et al. (CASENT9008673); 1F, 1Juv, Antananarivo, +Reserve +Speciale +d'Ambohitantely +, +Foret +d'Ambohitantely +, 20.9 km 72° NE Ankazobe, +18°13'31"S +, +47°17'13"E +, 1410 m., 17-22 Apr 2001, montane rainforest, EB17 beating low vegetation, Fisher, Griswold et al. (CASENT9001208). + + + +Etymology. +The specific name is a noun in apposition and commemorates Queen Rafohy. + + +Diagnosis. + +Males and females are considered part of the " +workmani +group" based on having a single dorsal protuberance on the abdomen (a triangular shaped abdomen) (Fig. 5A). Males are distinguished from the " +workmani +group" species +E. andriamanelo +sp. n., +E. ranavalona +sp. n., and +E. rangita +sp. n. by having a bifurcating MA (Fig. 5C), from +E. andrianampoinimerina +by lacking the distinctive abdomen markings (Fig. 5A), and +E. workmani +by lacking the large bump on the pedipalpal bulbs (Fig. 5 +D-K +). Females are distinguished from +E. andriamanelo +by lacking the heavily sclerotized +"T" +shaped structure on the posterior of the bursa, from +E. andrianampoinimerina +by lacking the strong abdomen markings and by the +"neck" +having a tilt angle that is less than 80°, and from +E. ranavalona +by lacking the lime-green abdomen markings. Females are indistinguishable from the remaining " +workmani +group" species. + + + +Description. + +Male holotype (CASENT9006503, from +Reserve +Speciale +d'Ambohitantely +, Madagascar). Total length 4.41, carapace 1.75 long, 1.29 wide. Abdomen 2.57 long, 1.29 wide, 2.91high, with a prominent dorsal hump. Carapace tilt angle 74.82°, tilt height (CtH) 3.93, constriction 0.56, head length 1.38, neck length 2.29. CtH divided by carapace length 2.25. Cephalon with AME on a large bulge and 4 post-ocular protrusions on the apex of the cephalon (Fig. 5A), each provided with a short modified spine at the tip. Chelicerae 4.02 long, and with spine 0.39 from base of chelicerae (Fig. 5A). Femur I 9.02 long. Sternum 1.12 long, 0.67 wide. Carapace, chelicerae, sternum and femora I & II reddish dark brown with many white setae. All coxae and legs III & IV yellowish brown. The latter with darker annulations on femora, tibiae and metatarsi. Abdomen yellowish brown, mottled with brown, and light brown book-lung covers, all covered with many white setae (Fig. 5A). Pedipalpal tegulum of the " +workmani +group" form, with apical conductor encircling a pit-like cavity (Fig. 5 +C-L +). Conductor tip is a broad triangular point similar to other " +workmani +group" species except +E. andriamanelo +sp. n. (Fig. 5 +D-L +). MA with a bifurcation (Fig. 5C, H, L). Embolus similar to other " +workmani +group" species, being broad and complex with the sperm duct opening in the middle and sclerotization only at the tip (Fig. 5 +D-E +, +G-H +, +J-K +). + + +Female paratype (CASENT9015039). Total length 4.60, carapace 1.69 long, 1.51 wide. Abdomen 2.65 long, 2.39 wide, 3.91 high, with dorsal hump. Carapace tilt angle 73.3°, tilt height (CtH) 4.00, constriction 0.59, head length 1.54, neck length 2.26. CtH divided by carapace length 2.37. Cephalon as in male. Chelicerae 3.99 long, and with spine 0.44 from base of chelicerae. Tarsus of pedipalps with ventral patch of long thick setae. Femur I 6.30 long. Sternum 1.10 long, 0.66 wide. Colors as in male, but generally darker. Female internal genitalia indistinguishable from other " +workmani +group" species (Fig. 5B). + + + +Figure 5. +Eriauchenius rafohy +sp. n. A male (CASENT9015039) habitus, lateral view, image reversed B female (CASENT9006503) internal genitalia, dorsal view +D-F +, L male right pedipalpal bulb (CASENT9004087), image reversed +G-K +left pedipalpal bulb (CASENT9015039) C median apophysis variation, apical view (CASENT9004087 & CASENT9015039) D, G, J prolateral view E, H, K ventral view F, I retrolateral view L close-up, ventral view. Scale bars: 1 mm (A); 0.25 mm (B, D). + + + + +Variation. +Total length 3.39-4.73 (males; n=4), 4.32-4.86 (females; n=6); Carapace length 1.50-1.80 (males; n=4), 1.57-1.75 (females; n=6); Femur I 5.10-5.72 times the length of carapace in males (n=4) and 3.48-3.88 times the length of carapace in females (n=6). CtH divided by carapace length 2.17-2.35 in males (n=4), 2.20-2.39 in females (n=6). Average femur I length 8.70 (males; n=4), 6.16 (females; n=6). + + +Natural history. +Specimens have been collected in montane rainforest through general collecting, beating vegetation, sweeping, raking, cryptic searching, and among fallen logs and litter in altitudes from 1300-1638 m above sea level. One specimen was collected with a hatched eggsac. + + +Distribution. +Known only from Antananarivo Province in central Madagascar (Fig. 30). + + + \ No newline at end of file diff --git a/data/38/75/13/387513D19B868BE0C77F6343D6EC120E.xml b/data/38/75/13/387513D19B868BE0C77F6343D6EC120E.xml new file mode 100644 index 00000000000..a18292427c6 --- /dev/null +++ b/data/38/75/13/387513D19B868BE0C77F6343D6EC120E.xml @@ -0,0 +1,225 @@ + + + +New records and detailed distribution and abundance of selected arthropod species collected between 1999 and 2011 in Azorean native forests + + + +Author + +Borges, Paulo A. V. + + + +Author + +Gaspar, Clara + + + +Author + +Crespo, Luis Carlos Fonseca + + + +Author + +Rigal, Francois + + + +Author + +Cardoso, Pedro + + + +Author + +Pereira, Fernando + + + +Author + +Rego, Carla + + + +Author + +Amorim, Isabel R. + + + +Author + +Melo, Catarina + + + +Author + +Aguiar, Carlos + + + +Author + +Andre, Genage + + + +Author + +Mendonca, Enesima P. + + + +Author + +Ribeiro, Servio + + + +Author + +Hortal, Joaquin + + + +Author + +Santos, Ana M. C. + + + +Author + +Barcelos, Luis + + + +Author + +Enghoff, Henrik + + + +Author + +Mahnert, Volker + + + +Author + +Pita, Margarida T. + + + +Author + +Ribes, Jordi + + + +Author + +Baz, Arturo + + + +Author + +Sousa, Antonio B. + + + +Author + +Vieira, Virgilio + + + +Author + +Wunderlich, Joerg + + + +Author + +Parmakelis, Aristeidis + + + +Author + +Whittaker, Robert J. + + + +Author + +Quartau, Jose Alberto + + + +Author + +Serrano, Artur R. M. + + + +Author + +Triantis, Kostas A. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +10948 +10948 + + + + +http://dx.doi.org/10.3897/BDJ.4.e10948 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e10948 +1314-2828-4-10948 + + + + +Geotomus punctulatus (A. Costa, 1847) + + + +Ecological interactions + +Native status +Native + + + +Distribution +FAI*; GRA; TER; SMG; SMR + + +Notes +Also present: MAD; CAN (Biogeographical Realm: Western Palearctic) + + + \ No newline at end of file diff --git a/data/38/75/3F/38753F427E8551758F97D4EC2347C0F3.xml b/data/38/75/3F/38753F427E8551758F97D4EC2347C0F3.xml new file mode 100644 index 00000000000..ff181c36463 --- /dev/null +++ b/data/38/75/3F/38753F427E8551758F97D4EC2347C0F3.xml @@ -0,0 +1,188 @@ + + + +A foundation monograph of Convolvulus L. (Convolvulaceae) + + + +Author + +Wood, John R. I. +Department of Plant Sciences, South Parks Road, University of Oxford, OX 1 3 RB, UK & Honorary Research Associate, Royal Botanic Gardens, Kew + + + +Author + +Williams, Bethany R. M. +Department of Plant Sciences, South Parks Road, University of Oxford, OX 1 3 RB, UK & Department of Life Sciences, Natural History Museum, Cromwell Road, London SW 7 5 BD, UK + + + +Author + +Mitchell, Thomas C. +Plant Biodiversity Research, Technische Universitaet Muenchen, Maximus-von-Imhof Forum 2, 85354 Freising, Germany + + + +Author + +Carine, Mark A. +Department of Life Sciences, Natural History Museum, Cromwell Road, London SW 7 5 BD, UK + + + +Author + +Harris, David J. +https://orcid.org/0000-0002-6801-2484 +Royal Botanic Garden Edinburgh, 20 A Inverleith Row, Edinburgh EH 3 5 LR, UK + + + +Author + +Scotland, Robert W. +Department of Plant Sciences, South Parks Road, University of Oxford, OX 1 3 RB, UK +robert.scotland@plants.ox.ac.uk + +text + + +PhytoKeys + + +2015 + +2015-06-18 + + +51 + + +1 +282 + + + + +http://dx.doi.org/10.3897/phytokeys.51.7104 + +journal article +http://dx.doi.org/10.3897/phytokeys.51.7104 +1314-2003-51-1 +E76E3938E216FF804849B803C469FE14 +576310 + + + + +121. +Convolvulus hamadae (Vved.) Petrov, Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol., n.ser., 44: 132. 1935. (Petrov 1935: 132). + + + + +Convolvulus subsericeus subsp. hamadae +Vved., Byull. Sredne-Aziatsk. Gosud. Univ. 15 (Suppl.): 32. 1927. ( +Popov and Vvedensky 1927 +: 32). Type. KAZAKHSTAN, Kara-tau, +Popov +5/6/1926 (holotype TAK; isotypes B, BM!, E!, K!, LE!, P!, W!.) + + + +Type. + +Based on +Convolvulus subsericeus subsp. hamadae +Vved. + + + +Description. + +Erect undershrub, intricately branched from the base to at least 40 cm; stems, thinly sericeous. Leaves 1-5 +x +0.2 cm, linear-oblong, acute, base tapering into a long pseudopetiole, thinly adpressed pubescent and appearing greenish. Flowers 1 (-2) at the apex of rigid, straight, relatively slender woody peduncles 0.8-1.5 cm long; bracteoles minute, linear, c. 1 mm, pedicels 0.5-1 mm, bent at 90° to peduncle; sepals (3-) 4 (-5) +x +1.5 mm, narrowly oblong, acute, densely pubescent; corolla (8-)10 mm, white, unlobed, broadly infundibuliform, midpetaline bands pilose, terminating in a tooth; ovary pilose. Capsule pilose, seeds pubescent. + + + +Distribution. + +Kazakhstan ( + +Drobov + +s.n. [3/8/1996], +Krasheninnikov +158); Kyrgyzstan ( +Knorring +115, +Drobov +246); Uzbekistan ( +Tishchenko +98, +Muravliansky +1932, +Knorring +60); Tajikistan ( +Nikitin +167, s.n. [19/6/1936], +Knorring +129); Turkmenistan ( +Litvinow +1647, +Sintenis +1285); Afghanistan ( +Aitchison +731); Iran ( +Pabot +DK 518). Most common in Uzbekistan. + + + +Notes. + +The indumentum and corolla size suggests this lies between + +Convolvulus erinaceus + +and + +Convolvulus subsericeus + +or more probably + +Convolvulus eremophilus + +, given the distribution of the three species. It has a laxer, less rigid appearance than + +Convolvulus erinaceus + +with branches less divaricate, the corolla is longer and unlobed and the sepals are acute, not obtuse. From + +Convolvulus subsericeus + +it is distinguished by the shorter, pungent branches, flowers generally solitary and a little smaller, the sepals acute, not acuminate. From + +Convolvulus eremophilus + +it is distinguished by the sparse, adpressed indumentum of the stems and shorter corolla. A few specimens are completely glabrous, such as +Botchantzev +468 from Uzbekistan, but seem to fit here best. + + +Sa'ad +treated this species as a synonym of + +Convolvulus erinaceus + +but the sepals and corolla are quite different. + + + + \ No newline at end of file diff --git a/data/38/75/5C/38755C7F12DDEC5F135D3FCAD0E03509.xml b/data/38/75/5C/38755C7F12DDEC5F135D3FCAD0E03509.xml new file mode 100644 index 00000000000..bf3280b0dde --- /dev/null +++ b/data/38/75/5C/38755C7F12DDEC5F135D3FCAD0E03509.xml @@ -0,0 +1,88 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part P) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +718 +782 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Polypodium fragrans +Linnaeus + +, + +Species Plantarum +2 + +: 1089. 1753 + + +. + + + +"Habitat in Sibiria." RCN: 7891. + + + + +Lectotype +(Bobrov in +Novosti Sist. Vyssh. Rast. +21: 9. 1984): +Amman 49 +, Herb. Linn. No. 1251.32 ( +LINN +) + +. + + + + +Current name: + +Dryopteris fragrans +(L.) Schott + +( +Polypodiaceae +). + + + + \ No newline at end of file diff --git a/data/38/75/87/38758798FFC2FFA8FF6777DEFEA2F48E.xml b/data/38/75/87/38758798FFC2FFA8FF6777DEFEA2F48E.xml new file mode 100644 index 00000000000..41b4554a764 --- /dev/null +++ b/data/38/75/87/38758798FFC2FFA8FF6777DEFEA2F48E.xml @@ -0,0 +1,293 @@ + + + +Description of four new species of Mesocletodes Sars, 1909 (Copepoda, Harpacticoida, Argestidae) and redescription of Mesocletodes robustus Por, 1965 from the South Atlantic, including remarks on the Mesocletodes abyssicola- group * + + + +Author + +Menzel, Lena + + + +Author + +George, Kai Horst + +text + + +Zootaxa + + +2009 + +2009-05-11 + + +2096 + + +1 + + +214 +256 + + + + +https://biotaxa.org/Zootaxa/article/view/zootaxa.2096.1.14 + +journal article +10.11646/zootaxa.2096.1.14 +1175-5326 +5320482 + + + + + + + +Mesocletodes meteorensis + +sp. nov. + + + + + + +( +Figs 18–24 +) + + +Etymology. +The name refers to the RV “Meteor”, on board of which the sample containing this species was taken. + + + +Locus typicus +: + + +Angola +Basin +, (off +Angola +), +RV +„Meteor“, Cruise M-48/1, + +27.07.2000 + + +. + + + + +Holotype +: + +1 female +, dissected, mounted on 7 slides, coll. no. +SMF +31424/1–7; at station 346/1 ( +16°17.0’S +/ +05°27.0’E +, + +5389m + +). + + + + + +Paratype +: + +1 female +, dissected, mounted on 10 slides, coll. no +SMF +31425/1–10 at station 346/3 ( +16°17.0’S +/ +05°27.0’E +, + +5389m + +) + +. + + +Description of female +. Habitus ( +Fig. 18 +) of cylindrical shape, no clear distinction between prosome and urosome. Body length 627µm. Rostrum small, not protruding, with 2 sensilla. Cphth with a dorsal cuticular process which is triangular, curved and pointing backwards. Process with several spinules. Cphth with several fine spinules. Distal margins of cphth and bodysomites with smooth hyaline frill. Long sensilla on distal margins of body somites, except the penultimate one. Spinules arranged in rows and decreasing in length posteriorly. Body blotched with small depressions (as depicted for telson). Genital double somite incompletely fused. + +Telson square, dorsally with bifid cuticular process peaked backwards: robust at the insertion, anterior and posterior peaks short, of equal length. Caudal region of telson with several rows of spinules, lateral to the process 1 sensillum on each side. + +A1 ( +Fig. 19A +) 8-segmented, acrothek on segments 4 and 8. First segment without seta but with 2 rows of spinules. Second segment with a strong protrusion bearing a strong bipinnate seta. Spines of A1 with 1 STE each. + +Setal formula: I:0, II:6, III:6, IV:2+Aes, V:1, VI:2, VII:4, VIII:6+Aes. + +A2 ( +Fig. 19B +) basis with fine spinules. Exp small, 1-segmented with 2 bipinnate setae of unequal length. Enp1 with few outer spinules. Enp2 covered by spinules, with 2 medial bipinnate spines with 1 STE each and 6 terminal elements. 1 outer bipinnate spine, 2 geniculated setae, 1 bipinnate seta, 1 bipinnate seta with STE, this seta fused to a small bare seta at the base. + + +Md ( +Figs 20E, F +) gnathobase with broad grinding face and 3 rows of spinules. Grinding face composed of 1 imbricate, distally carved seta, beneath 1 bare, spoon like seta, followed by several fused toothlike elements. Strong bare seta ventrally. Palpus 2- segmented with spinules. Basis with 1 seta (seta lost during preparation). Enp 1- segmented, with 4 terminal and 1 subterminal setae. Exopodal lobe with 2 bipinnate setae. + + +Mxl ( +Figs 20B, C +) arthrite of the praecoxa with long spinules and 10 armature elements: 2 bare surface setae (depicted beneath), 2 strong, tooth like setae with spinules, 1 strong, unarmed tooth like seta, 1 strong, undulated unipinnate seta, 1 brushlike seta, 1 compact, unipinnate seta, 1 slender, unipinnate seta, 1 strong, unipinnate seta. Coxa with long spinules and 5 setae, strongest seta brushlike, incompletely fused to coxa. Basis with 7 setae and several spinules. + + +Mx ( +Fig. 20A +) syncoxa with 2 endites. Proximal endite with 1 bare seta, distal endite with 3 setae: 1 strongly bipinnate and 2 bare setae. Basis with 2 strongly bipinnate setae and 2 bare setae. Enp 1-segmented, very small, with 2 bipinnate setae. + + +Mxp ( +Fig. 20D +) syncoxa with many fine spinules and 2 bipinnate setae of unequal length. Basis with fine outer and coarse inner spinules. Enp 1-segmented, fused to strong claw. + + +P1 ( +Fig. 21A +) coxa with several spinules. Basis with 1 inner and 1 outer spine, net-like structure close to outer seta. Exp 3-segmented. Exp1 and 2 without inner armature. Exp3 proximally with inner tube pore, 3 bipinnate spines with 1 STE each and 1 bare inner seta. Enp biarticulate. Enp1 with inner seta. Enp2 with 1 terminal, bipinnate spine, 1 terminal, bipinnate seta and 1 bare, inner seta. Setal formula as in +Table 4. + + +P +2–P +4 +( +Figs 21B +; +22A, B +) coxae with several spinules, bases with outer seta and inner setular tufts, netlike structure close to outer seta. Exp 3-segmented, increasing in length and decreasing in breadth from P2 to P4. Exp1 with 5 (P3) or 4 (P4) fine, inner spinules. Exp1 without inner seta. Exp2 with inner, bipinnate seta and outer spine. Exp3 of P2 and P3 with 2 bipinnate, outer spines and 2 bipinnate setae terminally. P4 Exp3 with 2 outer, bipinnate spines, 1 terminal bipinnate and 1 inner, bipinnate seta. Second terminal seta probably lost during sample treatment. Enp biarticulate. Enp1 with inner bipinnate seta. P2–P4 Enp2 with 1 outer, 2 terminal and 1 inner setae. Spines with spinules at their insertion points. Setal formula as in +Table 4. + + + +FIGURE 18: + +Mesocletodes meteorensis + +sp. nov. +, female (holotype). Habitus lateral view, with detail of overall surface structure illustrated on telson; scale bar: 50µm. + + + + +FIGURE 19: + +Mesocletodes meteorensis + +sp. nov. +, female (paratype). A, antennula; B, antenna; scale bars: 50µm. + + + + +FIGURE 20: + +Mesocletodes meteorensis + +sp. nov. +, female (holotype). A, maxilla; B, maxillula; C, maxillular palpus; D, maxilliped; E, mandibula gnathobasis; F, mandibular palpus; scale bar: 50µm. + + + + +FIGURE 21: + +Mesocletodes meteorensis + +sp. nov. +, female (paratype). A, P1; B, P2; scale bars: 50µm. + + + + +FIGURE 22: + +Mesocletodes meteorensis + +sp. nov. +, female (paratype). A, P3; B, P4; scale bars: 50µm. + + + + +FIGURE 23: + +Mesocletodes meteorensis + +sp. nov. +, female (holotype). P5; scale bar: 50µm. + + + + +FIGURE 24: + +Mesocletodes meteorensis + +sp. nov. +, female (holotype). telson and furcal rami lateral view; scale bar: 50µm. + + + + +FIGURE 25: + +Mesocletodes robustus + +, female. A, telson and furcal rami lateral view; B, habitus lateral view, with detail of surface structure of Cephalothorax and overall surface structure illustrated; scale bars: 50µm. + + + + +TABLE 4 +: + +Mesocletodes meteorensis + +sp. nov. +setal formula of P1–P5. + + + +P +5 +( +Fig. 23 +) basenp with several spinules. Outer lobe of basenp with setophore bearing 3 spinules and 1 outer seta. Inner lobe not protruding, with 1 inner, 1 median and 1 outer seta. The outer and median seta are close to each other, the long inner seta separated from the former two elements. Exp approximately 3 times longer than broad, with 5 setae and 1 terminal tube pore. Exp sparsely covered with spinules. Net-like structure between outer and inner lobe of basenp. Setal formula as in +Table 4 +. + + +Furcal rami ( +Fig. 24 +) approximately 3 times longer than wide (width measured at its base), insertion surrounded by spinules of anal somite. Furcal ramus with 7 setae: setae I and II ventral and lateral accompanied by 1 spinule each close to the insertion, seta III dorsally subterminal, setae IV and V terminal, seta VI ventrally terminal, seta VII in the middle of furcal ramus. Setae I, II, III, VI are bare, seta IV long and bipinnate, seta V short and bipinnate, seta VII triarticulate and bare. + +Male unknown. + + + \ No newline at end of file diff --git a/data/38/75/87/38758798FFD6FFB5FF67764DFA86F452.xml b/data/38/75/87/38758798FFD6FFB5FF67764DFA86F452.xml new file mode 100644 index 00000000000..002d95348b7 --- /dev/null +++ b/data/38/75/87/38758798FFD6FFB5FF67764DFA86F452.xml @@ -0,0 +1,119 @@ + + + +Description of four new species of Mesocletodes Sars, 1909 (Copepoda, Harpacticoida, Argestidae) and redescription of Mesocletodes robustus Por, 1965 from the South Atlantic, including remarks on the Mesocletodes abyssicola- group * + + + +Author + +Menzel, Lena + + + +Author + +George, Kai Horst + +text + + +Zootaxa + + +2009 + +2009-05-11 + + +2096 + + +1 + + +214 +256 + + + + +https://biotaxa.org/Zootaxa/article/view/zootaxa.2096.1.14 + +journal article +10.11646/zootaxa.2096.1.14 +1175-5326 +5320482 + + + + + + + +Mesocletodes +Sars, 1909 + + + + + + + + +Type +species: + + +Mesocletodes irrasus +(T. +Scott, 1894 +) + +(described as + +Cletodes irrasa + +) + + +Additional species: +In addition to the 4 herein new described species, + +Mesocletodes + +contains 32 species to date. + + +Diagnosis (amended by the authors). + +Body of subcylindric form, distal edge of body somites with many spinules close to hyaline frill, integument thin and flexible. Cphth comparatively short, rostrum small. Telson large, square. Furcal rami longer than broad. seta +VII +in the proximal third. +Antennula +: 7–8-segmented, second segment with strong protrusion bearing 1 strong bipinnate seta pointing backwards. +Antenna +with basis or allobasis, exp at most 1-segmented with at most 2 setae. +Mandibula +: palpus with exp and enp at most 1-segmented, elements of gnathobase form broad grinding face. +Maxilla +proximal endite with only 1 seta. +Mxp +stenopodial, with strong claw distally. +Swimming +legs: +Enp +at most biarticulate, small, equal in armature at each leg but increasing in length from P2–P4. +Exp +3-segmented, of P1 fairly small, of P2–P4 long and slender with slender inner setae. P1 exp3 with 4 setal elements only, spines with +Subapical Tubulate Extensions. P +5 exp long and slender, inner lobe of basenp barely protruding. +1 egg + +sack with 2– +40 eggs +. + + + + \ No newline at end of file diff --git a/data/38/75/87/38758798FFD6FFBFFF6774FEFE44F2A7.xml b/data/38/75/87/38758798FFD6FFBFFF6774FEFE44F2A7.xml new file mode 100644 index 00000000000..cd38fed072c --- /dev/null +++ b/data/38/75/87/38758798FFD6FFBFFF6774FEFE44F2A7.xml @@ -0,0 +1,260 @@ + + + +Description of four new species of Mesocletodes Sars, 1909 (Copepoda, Harpacticoida, Argestidae) and redescription of Mesocletodes robustus Por, 1965 from the South Atlantic, including remarks on the Mesocletodes abyssicola- group * + + + +Author + +Menzel, Lena + + + +Author + +George, Kai Horst + +text + + +Zootaxa + + +2009 + +2009-05-11 + + +2096 + + +1 + + +214 +256 + + + + +https://biotaxa.org/Zootaxa/article/view/zootaxa.2096.1.14 + +journal article +10.11646/zootaxa.2096.1.14 +1175-5326 +5320482 + + + + + + + +Mesocletodes angolaensis + +sp. nov. + + + + + + +( +Figs 2–6 +) + + +Etymology. +The species name refers to the sampling location, the +Angola +Basin. + + + +Locus typicus +: + + +Angola +Basin +(off +Angola +), +RV +„Meteor“, Cruise M-48/1, + +27.07.2000 + + +. + + + + +Holotype +: + +1 male +, dissected, mounted on 9 slides, coll. no. +SMF +31430/1–9 at station 346/1 ( +16°17’S +, +05°27’E +, + +5389m + +). + + + +Description of male. +Habitus ( +Figs 2 A, C, D +) of cylindrical shape. Body length 642µm. No clear distinction between prosome and urosome. Distal margins of cphth and free thoracic somites with denticulated, textured hyaline frill ( +Fig. 2B +) and, except the penultimate somite, with fine, long sensilla. Urosomites with long spinules inserting just anteriorly of the hyaline frill. Rostrum not protruding, with 2 sensilla. Cphth without cuticular process, dorsally and laterally with slight depressions, cuticula with nearly symmetric pattern and symmetrically arranged sensilla. Ventral margin of cphth with small spinules and few sensilla. Telson nearly square from dorsal view, slightly tapering posteriorly, ventrally with spinules, dorsally with strong, cuticular process ( +Fig. 6A +). Cuticular process on telson with basal swelling, distally peaked, long and narrow. Laterally with 1 sensillum on each side. Lateral edges of pleurotergites of P2–P4 bearing prosomites with thickened cuticula and several spinules. P3–P4 bearing somites with 2 dorsal hyaline protrusions each bearing a long sensillum and, laterally of these, a row of spinules. P5 bearing somite laterally with 2 rows of small spinules and few strong spinules close to the hyaline frill. + + +A1 ( +Fig. 3A +) 7-segmented, haplocer, acrothek on segments IV and VII. First segment without seta, ornamented with strong spinules proximally and subdistally, with small spinules subdistally on anterior face. Second segment with a strong protrusion bearing a strong, bipinnate seta. Segment III very short. Aes of segment IV extremely elongate and large. Segments IV and V with 2 and 1 tripinnate seta(e) respectively. Segments IV–VII arranged in a loop. Spines of A1 with 1 STE each. + +Setal Formula: I:0, II:7, III:3, IV:5+Aes, V:2, VI:2, VII:7+Aes. + +A2 ( +Fig. 3B +) with basis, seemingly without exp. Enp1 with 6 long spinules. Enp2 with 3 long and several small spinules, 2 medial spines with 1 STE each, terminally with 4 bipinnate setae, 2 of which geniculated. + +Mouthparts atrophied, could not be traced due to their strong reduction. + + +FIGURE 2: + +Mesocletodes angolaensis + +sp. nov. +, male. A, habitus dorsal view, cephalothorax and thorax; B, structure of hyaline frill at distal margins of body somites; C, habitus lateral view, cephalothorax and thorax; D, habitus lateral view, urosome; scale bars: 50µm. + + + + +FIGURE 3: + +Mesocletodes angolaensis + +sp. nov. +, male. A, antennula; B, antenna; scale bars: 50µm. + + + + +FIGURE 4: + +Mesocletodes angolaensis + +sp. nov. +, male. A, P1; B, P2; scale bars: 50µm. + + + + +FIGURE 5: + +Mesocletodes angolaensis + +sp. nov. +, male. A, P3; B, P4; C, P4 coxa and basis; scale bar: 50µm. + + + + +FIGURE 6: + +Mesocletodes angolaensis + +sp. nov. +, male. A, telson and furcal rami lateral view, arrow highlighting distal tube pore; B, P5; scale bars: 50µm. + + + +P1 ( +Fig. 4A +) coxa with several rows of spinules, with fine spinules close to inner and with coarser spinules close to outer margin. Basis at inner margin with setular tuft, with 1 inner and 1 outer spine. Exp 3- segmented. Exp1 and Exp2 without inner armature. Exp3 with 1 outer bipinnate spine with STE, 2 terminal and 1 inner, bipinnate seta. Enp 2-segmented. Enp1 without inner seta, Enp2 with 1 inner, 1 terminal and 1 outer, bipinnate seta. Outer seta short and with STE. All segments with inner setules and outer spinules. Spinules near insertion of spines. Intercoxal sclerites are U-shaped and bare. Setal formula as in +Table 1. + + + +TABLE 1 +: + +Mesocletodes angolaensis + +sp. nov. +setal formula of swimming legs P1–P5 + + + + + + + + + + + + + + + + + + + + + + + + + +
ExpEnp
P1
P2
P3
P4
P52-1-11-1-0
+
+ +P +2–P +4 +( +Figs 4B +; +5A, B, C +) coxa with spinules as shown for P3. Basis with inner setular tufts and outer seta (as illustrated for P4). Exp 3-segmented. Exp1 with fine spinules at inner margin. Exp2 with inner, bipinnate seta. Exp3 with 2 outer, bipinnate spines, 1 terminal, unequally bipinnate spine and 1 bipinnate seta, with 2 (P2 and P3) or 1 (P4) inner, bipinnate seta(e). Enp biarticulate. Enp1 with inner, bipinnate seta and fine, outer spinules. Enp2 of P2 and P3 with 4 bipinnate setae, Enp2 of P4 lost during dissection. Spinules near insertion of spines. Intercoxal sclerite as in P1. Setal formula as in +Table 1. + + +P +5 +( +Fig. 6B +) outer part of basenp with setophore, 3 spinules and long bipinnate seta. Inner part of basenp barely protruding, with 1 long, strong, inner seta and 1 short, bare, outer seta. Exp about 4 times longer than basal width, proximally with 2 long spinules, 2 outer, 1 terminal and 1 inner setae and 1 STE. Setal formula as in +Table 1. + + +P +6 +reduced to 1 seta. + + +Furcal rami ( +Fig. 6A +) about 13 times longer than wide at their insertion. Entirely covered by spinules, insertion surrounded by coarse spinules of anal somite. Furcal ramus with 7 setae: I and II close together laterally in proximal third, seta III inserted subdistally dorsolaterally, IV, V and VI inserting terminally, VII dorsally in the middle. Setae I, II, III, IV and VI bare, Seta V broken, seta VII triarticulated and bare. Furcal ramus with tube pore terminolaterally (highlighted by arrow in +Fig. 6A +). + +Female unknown. +
+
+
\ No newline at end of file diff --git a/data/38/75/87/38758798FFDAFFA5FF6771EAFEA2F0FD.xml b/data/38/75/87/38758798FFDAFFA5FF6771EAFEA2F0FD.xml new file mode 100644 index 00000000000..d961a64222c --- /dev/null +++ b/data/38/75/87/38758798FFDAFFA5FF6771EAFEA2F0FD.xml @@ -0,0 +1,279 @@ + + + +Description of four new species of Mesocletodes Sars, 1909 (Copepoda, Harpacticoida, Argestidae) and redescription of Mesocletodes robustus Por, 1965 from the South Atlantic, including remarks on the Mesocletodes abyssicola- group * + + + +Author + +Menzel, Lena + + + +Author + +George, Kai Horst + +text + + +Zootaxa + + +2009 + +2009-05-11 + + +2096 + + +1 + + +214 +256 + + + + +https://biotaxa.org/Zootaxa/article/view/zootaxa.2096.1.14 + +journal article +10.11646/zootaxa.2096.1.14 +1175-5326 +5320482 + + + + + + + +Mesocletodes dorsiprocessus + +sp. nov. + + + + + + +( +Figs 12–17 +) + + +Etymology. +The name refers to the bifid cuticular processes in P2–P5-bearing somites and first urosomite. + + + +Locus typicus +: + + +Angola +Basin +, (off +Angola +), +RV +„Meteor“, Cruise M-48/1, + +27.07.2000 + + +. + + + + +Holotype +: + +1 female +, dissected, mounted on 12 slides, coll. no. +SMF +31428/1–12 at station 346/4 ( +16°16.9’S +/ +05°27.0’E +, + +5389m + +). + + + + + +Paratype +: + +1 female +mounted on 1 slide, coll. no. +SMF +31429/1 at station EBS 340 (start: +18°18.3’S +004°41.3’E +; end +18°19.4’S +004°41.9’E +, + +5395m + +) + +. + + +Description of female. +Habitus ( +Fig. 12A +) of cylindrical shape, no clear distinction between prosome and urosome. Body length 1105µm. Rostrum small, not protruding, with 2 sensilla. Cphth dorsally with cuticular process, process triangular, curved posteriorly. Distal margins of cphth and body somites with denticulated hyaline frill. Long sensilla on distal margins of body somites, except the penultimate one. Body somites with rows of spinules, increasing in length and breadth posteriorly. P3–P5 bearing somites and second urosomite dorsally with bifid cuticular processes. Telson quadrate, with several strong spinules and bifid cuticular process dorsally, peaked upward, posterior tip longer than anterior. Laterally, 1 sensillum on each side. Genital doublesomite incompletely fused. P2–P4 bearing somites with thickened cuticula near insertion of the legs. + + +A1 ( +Fig. 13A +) 8-segmented, acrothek on segments 4 and 8 proximally with corona of spinules and several spinules scattered across the surface. Second segment with strong protrusion bearing a strong, bipinnate seta. Third segment elongated. Spines of A1 with 1 STE each. All segments covered by fine spinules. + +Setal formula: I:0, II:8, III:5, IV:2+Aes, V:1, VI:3, VII:6; VIII: 6+Aes. + +A2 ( +Fig. 15A +) coxa short and unarmed. Basis with fine spinules. Exp 1-segmented, with 2 bipinnate setae. Enp1 and 2 with fine, inner spinules and 4 outer spinules each. Enp2 with 2 medial, bipinnate spines with 1 STE each and 6 terminal elements. 1 outer bipinnate spine, 2 geniculated, bare setae, 1 bipinnate spine, 1 bipinnate spine with STE, spine fused with 1 fine bare seta at the basis. + + +Paragnaths ( +Fig. 13B +) with few short, fine spinules medially and many very long spinules laterally, ventrally of these long spinules are broad spinules with distal brushes; ventral surface covered in small spinules. + + +Md ( +Figs 14B, C +) gnathobase with broad grinding face. Dorsally with transformed denticulated seta, beneath 2 spoonlike setae, followed by several strong toothlike elements. Palpus 1-segmented, with spinules and 1 basal seta, 1 exopodal and 1 endopodal seta. + +Mxl lost during preparation. + +Mx ( +Fig. 14A +) syncoxa with 2 endites. Proximal endite with 1 seta, distal endite well developed with 3 terminal setae: 1 strongly bipinnate seta incompletely fused to the endite, 1 bipinnate and 1 bare seta. Basis with long spinules and 3 setae: 1 seta incompletely fused to basis, 1 strong seta and 1 bare seta subterminally. Enp 1-segmented, very small, with 2 setae. + + +Mxp ( +Fig. 13C +) syncoxa with 1 tripinnate seta, many very fine spinules and 3 rows of strong spinules. Basis with long inner spinules and many spinules dorsally. Enp 1-segmented, fused to strong claw (broken off). + + +P1 ( +Fig. 16A +) coxa with several spinules. Basis with 1inner and 1 outer spine. Exp 3-segmented. Exp1 and 2 inner margin without armature. Exp3 with 2 bipinnate spines with 1 STE each, 1 bipinnate seta terminally and 1 bare inner seta. Enp biarticulate. Enp1 with 1 bare inner seta. Enp2 with 1 bare inner seta and 1 bipinnate and 1 bare seta terminally. Strong spinules at insertions of spines, all segments with fine spinules. Setal formula as in +Table 3. + + +P +2–P +4 +( +Figs 16B +; +17A, B +) coxae with several spinules. Bases with outer seta only. Exp 3-segmented. Exp1 with hairy outer spinules, without inner seta. Exp2 with inner bipinnate seta and outer spine. Exp3 with 2 bipinnate outer spines, 2 bipinnate setae terminally and 2 (P2 and P3) or 1 (P4) inner bipinnate setae. The terminal outer spine of P4 Exp3 is probably broken off. Enp biarticulate. Enp1 with bare inner seta. Enp2 with 3 setae (P2) or with 2 setae (P3 and P4). All spines with spinules at their insertion points. Setal formula as in +Table 3. + + + +TABLE 3 +: + +Mesocletodes dorsiprocessus + +sp. nov. +setal formula of P1–P5. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
ExpEnp
P1I-0, I-0, I-2-10-1, 1-2-0
P2I-0, I-1, II-2-20-1, 1-2-0
P3I-0, I-1, II-2-20-1, 0-2-0
P4I-0, I-1, II-2-10-1, 0-2-0
P53-1-11-1-0
+
+ + +FIGURE 12: + +Mesocletodes dorsiprocessus + +sp. nov. +, female (holotype). A, habitus lateral view; B, telson and furcal rami lateral view; scale bars: 50µm. + + + + +FIGURE 13: + +Mesocletodes dorsiprocessus + +sp. nov. +, female (holotype). A, antennula; B, paragnaths; C, maxilliped; scale bars: 50µm. + + + + +FIGURE 14: + +Mesocletodes dorsiprocessus + +sp. nov. +, female (holotype). A, maxilla; B, mandibula; C, mandibular palpus; scale bar: 50µm. + + + +P +5 +( +Fig. 15B +) basenp with several spinules. Outer lobe of basenp with setophore bearing 3 spinules and 1 outer seta. Inner lobe not protruding, with 1 short outer and 1 long median bipinnate seta (lost during preparation, only insertion point remained). Net-like structure between inner and outer lobe of basenp. Exp approximately 9 times longer than broad, with 5 setae and 1 terminal tube pore. Exp covered with spinules. Setal formula as in +Table 3 +. + + +Furcal rami ( +Fig. 12B +) approximately 13 times longer than broad (the widest part measured at its base), the insertion surrounded by spinules of anal somite. Furcal ramus completely covered by spinules, with strong terminal tube pore and 7 setae: I and II in the middle of caudal ramus, seta III subdistally, setae IV, V and VI distally, seta VII dorsally in distal half. Seta I, III, IV and V lost during preparation, seta I and VI bare, seta VII triarticulate and bare. + +Male unknown. +
+
+
\ No newline at end of file diff --git a/data/38/75/87/38758798FFDCFFB9FF67714CFEA2F6CC.xml b/data/38/75/87/38758798FFDCFFB9FF67714CFEA2F6CC.xml new file mode 100644 index 00000000000..2cca665a6df --- /dev/null +++ b/data/38/75/87/38758798FFDCFFB9FF67714CFEA2F6CC.xml @@ -0,0 +1,329 @@ + + + +Description of four new species of Mesocletodes Sars, 1909 (Copepoda, Harpacticoida, Argestidae) and redescription of Mesocletodes robustus Por, 1965 from the South Atlantic, including remarks on the Mesocletodes abyssicola- group * + + + +Author + +Menzel, Lena + + + +Author + +George, Kai Horst + +text + + +Zootaxa + + +2009 + +2009-05-11 + + +2096 + + +1 + + +214 +256 + + + + +https://biotaxa.org/Zootaxa/article/view/zootaxa.2096.1.14 + +journal article +10.11646/zootaxa.2096.1.14 +1175-5326 +5320482 + + + + + + + +Mesocletodes bicornis + +sp. nov. + + + + + + +( +Figs 7–11 +) + + +Etymology. +The name refers to the double cuticular process on the cephalothorax. + + + +Locus typicus +: + + +Angola +Basin +, (off +Angola +), +RV +„Meteor“, Cruise M-48/1, + +27.07.2000 + + +. + + + + +Holotype +: + +1 female +, mounted on 1 slide, coll. no. +SMF +31426/1 at station 346/4 ( +16°16.9’S +/ +05°27.0’E +, + +5389m + +). + + + + + +Paratypes +: + +1 female +, dissected, mounted on 12 slides, coll. no. +SMF +31427/1–12 at station 346/2 ( +16°17.0’S +/ +05°27.0’E +, + +5389m + +) + +; + +1 female +, dissected, mounted on 6 slides, coll. no. +SMF +31431/1–6 at station 346/8( +16°17.0’S +/ +05°27.0’E +, + +5390m + +) + +; + +1 female +, mounted on 1 slide, coll. no. +SMF +31432/1 at station 346/2 ( +16°17.0’S +/ +05°27.0’E +, + +5389m + +) + +; + +1 female +, mounted on 1 slide, coll. no. +SMF +31433/1 at station 346/5 ( +16°17.0’S +/ +05°27.0’E +, + +5389m + +) + +; + +1 female +, mounted on 1 slide, coll. no. +SMF +31434/1 at station 346/1 ( +16°17.0’S +/ +05°27.0’E +, + +5389m + +) + +. + + + +FIGURE 7: + +Mesocletodes bicornis + +sp. nov. +, female (holotype). A, habitus lateral view; B, telson and furcal rami, lateral view; scale bar: 50µm. + + + + +FIGURE 8: + +Mesocletodes bicornis + +sp. nov. +, female (paratype). A, antennula; B, antenna; scale bars: 50µm. + + + + +FIGURE 9: + +Mesocletodes bicornis + +sp. nov. +, female (paratype). A, maxillula; B, maxilla; C, mandibula; D, maxilliped; E, P1; scale bars: 50µm. + + + +Description of female. +Habitus ( +Fig. 7A +) of cylindrical shape, no clear distinction between prosome and urosome. Body length 660µm. Rostrum small, not protruding, with 2 sensilla. Cphth dorsally with bifid, cuticular process, anterior part triangular, curved and pointing posteriorly, posterior part small and stout, triangular. Distal margins of cphth to second urosomite with denticulated, hyaline frill, the remaining urosomites with bare hyaline frill. Long sensilla on distal margins of body somites, except the penultimate one. P3–P5 bearing somites and second urosomite dorsally with bifid cuticular processes. Rows of spinules along posterior margins of somites, spinules increasing in length posteriorly. Telson square, dorsally with bifid, cuticular process peaked upward with posterior tip longer than the anterior one. + + +A1 ( +Fig. 8A +) 8-segmented, acrothek on segments 4 and 8. First segment without seta, proximally with corona of spinules and several spinules spread over the segment. Second segment with a strong protrusion bearing a strong, bipinnate seta. Third segment elongate, with 5 fine, long spinules at inner margin of the segment. Spines of A1 with 1 STE each. + +Setal formula: I:0, II:7, III:5, IV:2+Aes, V:1, VI:2, VII:3, VIII:6+Aes. + +A2 ( +Fig. 8B +) basis with fine spinules. Exp incompletely fused to basis, 1-segmented, with 1 long, bipinnate and 1 short, bare seta. Enp1 with many fine, long spinules, a corona of spinules in the distal part and 3 strong spinules at the outer margin. Enp2 with 4 strong outer spinules, 2 medial bipinnate spines with 1 STE each and 6 terminal elements: 1 outer, bipinnate spine, 1 annulate seta, 2 geniculated setae with 3 pinnae each, 1 annulate seta distally with STE, seta fused to a small, bare seta at the base. + + +Md ( +Fig. 9C +) gnathobase with broad grinding face. Dorsally with transformed denticulated seta, beneath 2 spoonlike setae, followed by several strong toothlike elements. Palpus 1-segmented, with 1 bipinnate basal seta, 1 bipinnate exopodal seta and 4 endopodal setae, 3 of these located terminally. + + +Mxl ( +Fig. 9A +) arthrite of the praecoxa with long spinules and 10 armature elements: 2 bare surface setae (depicted beneath), 2 strong, tooth like setae with 1 strong spinule each, 1 strong, tooth like seta with 1 spinule and several strong pinnae, 2 brushlike setae, 1 unipinnate seta, 1 bare, 1 unipinnate, single seta. Coxa with spinules at the base of arthrite, with long spinules and 5 setae, strongest seta fused to coxa. Basis with 5 bipinnate setae and 4 spinules. + + +Mx ( +Fig. 9B +) syncoxa with 2 endites. Proximal endite with 1 seta (seta lost during dissection), distal endite with 3 setae: Endite drawn out into strong claw with two accompanying bare setae. Basis with a row of small spinules and 3 setae: main seta incompletely fused to basis, 1 strongly bipinnate seta and 1 bare slender seta subterminally. Enp 1-segmented, very small, with 2 bipinnate setae. + + +Mxp ( +Fig. 9D +) syncoxa lost during preparation. Basis with many fine spinules, unarmed. Enp 1- segmented, fused to strong claw. + + +P1 ( +Fig. 9E +) coxa with several spinules. Basis with 1 inner and 1 outer spine. Exp 3-segmented. Exp1 and exp2 without inner armature. Exp3 inner seta transformed to tube pore. Exp3 with 3 bipinnate spines with 1 STE each. Enp biarticulate. Enp1 with inner seta. Enp2 with 2 terminal setae. Setal formula as in +Table 2. + + +P2–P +4 +( +Figs 10A–C +) coxae with several spinules (P2 lost during preparation. However, it was observed that P2 and P3 were identical with respect to the setation). Bases with outer seta and inner setular tufts. Exp 3- segmented. Exp1 P3 and P4 with few fine, inner spinules. Exp2 with inner, bipinnate seta and outer spine. Exp3 with 2 bipinnate, outer spines, 2 bipinnate setae terminally and 2 (P2 and P3) or 1 (P4) inner bipinnate setae. Enp biarticulate. Enp1 without seta. Enp2 with 4 bare setae. Spines with spinules at their insertionpoints. Setal formula as in +Table 2. + + + +TABLE 2 +: + +Mesocletodes bicornis + +sp. nov. +setal formula of swimming legs P1–P5. + + + + + + + + + + + + + + + + + + + +
P1
P2
P3
P4
P5
+
+ + +FIGURE 10: + +Mesocletodes bicornis + +sp. nov. +, female (paratype). A, P3; B, P3 coxa and basis; C, P4; scale bar: 50µm. + + + +P +5 +( +Fig. 11 +) basenp with several spinules. Outer lobe of basenp with setophore bearing 3 spinules and 1 outer seta. Inner lobe not protruding, with 1 long inner, 1 long median, bipinnate and 1 short, outer seta. The outer and median seta are close to each other, the long, inner seta separated from the former two elements. Exp approximately 5 times longer than broad, with 5 setae and 1 apical tube pore. Exp sparsely covered with spinules. Setal formula as in +Table 2 +. + + +Furcal rami ( +Fig. 7B +) approximately 13 times longer than broad (the widest part measured at its base), the insertion surrounded by spinules of anal somite. Furcal ramus with distal tube pore and 7 setae: setae I and II in the middle of caudal ramus with spinules at their insertions, seta III subdistally, setae IV and V distally, seta VI distally and arising ventrally, seta VII dorsally in distal half. Setae I and II bare, setae III, IV, V lost during sample treatment, seta VI bare, VII triarticulate and bare. + +Male unknown. +
+
+
\ No newline at end of file diff --git a/data/38/75/98/387598D11A749365E489DB8F354C4E7C.xml b/data/38/75/98/387598D11A749365E489DB8F354C4E7C.xml new file mode 100644 index 00000000000..e32f34fbbf4 --- /dev/null +++ b/data/38/75/98/387598D11A749365E489DB8F354C4E7C.xml @@ -0,0 +1,205 @@ + + + +Monogenea of fishes from the lagoon flats of Palmyra Atoll in the Central Pacific + + + +Author + +Vidal-Martinez, Victor Manuel + + + +Author + +Soler-Jimenez, Lilia Catherinne + + + +Author + +Aguirre-Macedo, Ma. Leopoldina + + + +Author + +Mclaughlin, John + + + +Author + +Jaramillo, Alejandra G. + + + +Author + +Shaw 2, Jenny C. + + + +Author + +James, Anna + + + +Author + +Hechinger, Ryan F. + + + +Author + +Kuris, Armand M. + + + +Author + +Lafferty, Kevin D. + +text + + +ZooKeys + + +2017 + +713 + + +1 +23 + + + + +http://dx.doi.org/10.3897/zookeys.713.14732 + +journal article +http://dx.doi.org/10.3897/zookeys.713.14732 +1313-2970-713-1 +D70E71F8669C4557B266D4FF8359A511 + + + + +Haliotrema aurigae (Yamaguti, 1968) Plaisance, Bouamer & Morand, 2004 + + + +Type host. + +Chaetodon auriga +( +Chaetodotidae +). + + + +Other host and localities. + +Chaetodon auriga +from +Hawai'i +( +Yamaguti 1968 +). On +C. auriga +, +C. citrinellus +, +C. vagabundus +, +C. ephippium +, +C. lunulatus +, +C. kleinii +, +C. lunula +, +C. ornatissimus +, +C. reticulatus +, +C. trifascialis +and +H. chrysostomus +from several sites of the Indo-West Pacific Ocean (Palau Micronesia, Moorea French Polynesia, Wallis and Futuna, New Caledonia, Heron Island and Lizard Island, Australia) ( +Plaisance et al. 2004 +). +Recently +, this species was reported on +C. auriga +from off the Pratas Islands, South China Sea ( +Kritsky et al. 2009 +) and +Hawai'i +( +Palm and Bray 2014 +) (all +Chaetodotidae +). + + + +Current host. + +Chaetodon auriga +and +Chaetodon lunula +( +Chaetodotidae +). + + + +Site infection. +Gills. + + +Prevalence and mean intensity. + +30,8 and 61 ++/- +49 (n=13) to +C. auriga +and 35,7 and 66 ++/- +20 (n=14) to +C. lunula +. + +Specimens deposited: CHCM No. 545 (paratypes) (1 slide, 3 specimens), USNM No. 1459845 (voucher) (1 slide, 6 specimen). + + +Remarks. + +This species was described for the first time by +Yamaguti (1968) +as +Pseudohaliotrematoides aurigae +. In 2004, Plaisance et al. recorded this species from 10 species of +Chaetodon +and one species of +Heniochus +( +Chaetodontidae +), and transferred it to the genus +Haliotrema +as +H. aurigae +. +Haliotrema aurigae +presents a tubular MCO bent near base base; base trapezoid; filamentous accessory piece, elongated, serving as a guide for the distal portion of the MCO. Dorsal anchor base/shaft junction hinged, with elongate superficial root and short, deep root. Ventral anchor with short roots and broad, slightly fenestrated base. Dorsal bar straight, bone-shaped. Ventral bar rod-shaped, an inverted broad U. New geographical record for Palmyra Atoll. + + + + \ No newline at end of file diff --git a/data/38/76/5D/38765D6F798B643AE71982FDFAD5C3B1.xml b/data/38/76/5D/38765D6F798B643AE71982FDFAD5C3B1.xml new file mode 100644 index 00000000000..76077d6b584 --- /dev/null +++ b/data/38/76/5D/38765D6F798B643AE71982FDFAD5C3B1.xml @@ -0,0 +1,65 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828--9042 + + + + +Endasys testaceipes (Brischke, 1881) + + + + +Phygadeuon testaceipes +Brischke, 1881 + + +coxalis +(Schmiedeknecht, 1905, +Stylocryptus +) + + + +Distribution +England + + +Notes + +added by +Sawoniewicz and Luhman (1992) + + + + \ No newline at end of file diff --git a/data/38/76/85/3876854331EEFB3C667A1560C82DB781.xml b/data/38/76/85/3876854331EEFB3C667A1560C82DB781.xml new file mode 100644 index 00000000000..dbddcbca8b8 --- /dev/null +++ b/data/38/76/85/3876854331EEFB3C667A1560C82DB781.xml @@ -0,0 +1,141 @@ + + + +Review of the ant genus Nesomyrmex (Hymenoptera: Formicidae: Myrmicinae) in southern Africa. + + + +Author + +Mbanyana, N. + + + +Author + +Robertson, H. G. + +text + + +African Natural History + + +2008 + +4 + + +35 +55 + + + + +http://antbase.org/ants/publications/23052/23052.pdf + +journal article +23052 + + + + +Nesomyrmex larsenae +sp. nov. + + + +Fig. 2m -o +Description of worker +Holotype. HL 0.698, HW 0.529, HW1 0.562, CI 76, SL 0.443, SI 84, PW 0.418, ML 0.861, EL 0.197, EI 37. + +Mandibles with fine longitudinal striations. Clypeus predominantly smooth, with weak longitudinal striations. Entire anterior margin of clypeus evenly convex. Eyes with 16 ommatidia in a longest row. Scapes relatively short (SI <85). With head in dorsal view hind margin convex. With mesosoma in profile, dorsal margins of promesonotum and propodeum each convex, with metanotal groove conspicuously impressed. Propodeum hump-shaped in profile, unarmed, with dorsum rounding evenly into declivity. Metapleural lobes low and rounded. Anterior peduncle long and narrow. Subpetiolar process vestigial, visible as a shallow obtuse angle. Petiolar node in profile massive and nodiform with anterior face angled at about 45° whereas posterior face is nearly vertical. Postpetiole low and rounded. Ventral margin of postpetiole in profile obtusely angled, without distinct process. Dorsum of head weakly shining with faint reticulate ground-sculpture; weakly striated between the eyes and more strongly striated between base of antenna and the eyes. Promesonotal dorsum finely reticulate. Propodeal dorsum with irregular reticulate ground sculpture overlaid by faint irregular transverse striations. Base of declivity with strongly developed transverse striations. Petiolar node and postpetiole with irregular sculpture; transverse striations on peduncle and vestigial transverse striations on petiolar node. Base of first gastral tergite witha ring ofshort costulae; remainder of the tergite predominantly shiny with weak reticulate pattern. Dorsum of head and mesosoma with appressed white, scattered pubescence, no erect hairs. The venter of head with three straight hairs. Propodeum without hairs. Petiolar node and postpetiole each with a pair of backwardly projecting fine long acute hairs in each. First gastral tergite with scattered, short, decumbent hairs, acute apically; with longer erect hairs along the posterior margin +and +on the sternite. Colour brick red with gaster dark brown. + + +Paratypes +. HL 0.688-0.718, HW 0.531-0.541, HW1 0.565-0.590, CI 75-77, SL 0.462-0.470, SI 87, PW 0.393-0.423, ML 0.859-0.895, EL 0.194-0.207, EI 36-38 (2 of 2 measured). Same data as holotype. + + + +Diagnosis + +Among the species without hairs on the propodeum ( +N. larsenae +, +N. ruani +, +N. entabeni +and +N. nanniae +), +N. larsenae +is distinguished by lacking erect hairs on the promesonotum, and also distinguished by its hump-shaped propodeum and by the brick red colour, with gaster dark brown; the other three species have erect hairs on the promesonotum, the propodeum forms an even convexity (not hump-shaped), and their colour is uniformly medium brown. + + + +Biology +Two specimens were collected from pitfall traps and one specimen from sweeping vegetation inSucculent Karoo near Nieuwoudtville in the Northern Cape. Probably ground-nesting but sweep sample shows that it does forage in vegetation. + + +Etymology +Named after Dawn Larsen, one of the collectors, who is an Assistant Collections Manager in the entomology collection of the Iziko South African Museum. + + +Material examined + + +Holotype +: +South Africa +: +Northern Cape +: west of +Driefontein +farm, +Succulent Karoo 2 site +( + +10.7 km +109° ESE + +Nieuwoudtville +), +31°22.581'S +19°13.507'E +, + +12-19 October 2000 + +, +H.G. Robertson +, +D. Larsen +& +R. Adams +; +NW00-SK2- P05 +, +SAM-HYM-C019131 + +. + + + +Paratype +workers +with same data as holotype except +NW00-SK2-P04 +, +SAM-HYM-C019130 +, +NW00-SK2-Sweep 228 +, +SAM-HYM-C019132 + +. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB1EFFD4FC84FC71FD2BF95D.xml b/data/38/76/87/387687E2BB1EFFD4FC84FC71FD2BF95D.xml new file mode 100644 index 00000000000..394318f1085 --- /dev/null +++ b/data/38/76/87/387687E2BB1EFFD4FC84FC71FD2BF95D.xml @@ -0,0 +1,268 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +1. + +Paracostus englerianus +(K.Schum.) C.D.Specht + + +— +Plate 1e +; +Map 15 + + + + + + +Paracostus englerianus +(K.Schum.) C.D.Specht + +in Specht & Stevenson (2006) 162. — + +Costus englerianus +K.Schum. (1892) + +419, t. 13 ( + +2 Aug. 1892 + +); (1904) 424. — +Type +: +Preuss 461 +(holo +B +destroyed), +Cameroon +, +W of Barombi-ba-Mbu +, + +2 Sept. 1890 + +. + + +As the holotype in B has been de- stroyed,the illustration accompanying the protologue ( +K.Schumann 1892: Tafel 13 +), which is the only remaining original material, is here designated as the +lectotype + +. + + + + + + +Costus unifolius +N.E.Br. (1892) + +696 ( + +10 Dec. 1892 + +), syn.nov. — +Type +: +Cultivated in Kew Gardens in 1892 from material received from Sander & Co. +, who collected it in +1891 in +Ghana +(‘ +Gold Coast’ +) (holo +K +) + +. + + + + +Terrestrial, prostrate herb +0.2–0.3 m +tall; rhizomes> +20 cm +long, repeatedly branched, horizontally creeping, +1.5–7 mm +diam, shoots reddish, provided with brown membranous sheaths 1.2–1.9 by +0.5–0.8 cm +and roots with side roots to c. +10 cm +long. +Leaves +1 per shoot; description of sheaths see under inflorescence; ligule and petiole absent; lamina green to shiny dark green above, paler green to whitish green below, elliptic to obovate or broadly so, 8–19 by +5–13 cm +, 3–4-plicate, glabrous on both sides, base attenuate, extreme base of leaf fleshy, +10–20 mm +long, at an angle of 45° with the lamina, sur- rounding the inflorescence, apex obtuse, minutely apiculate. +Inflorescence +axillary, 1–7-flowered, +0.5–1.3 cm +long, the lower portion enclosed by the more or less overlapping margins of the base of the lamina and by the uppermost 1–3 sheathing leaf bases; sheaths to c. 6 by +1.3 cm +, apex acute to obtuse; bracts, bracteoles and calyx rather densely covered with soft, erect hairs c. +1 mm +long, ovary glabrous; bracts reddish brown, green, or yellow, membranous, broadly to depressed ovate, 0.7–1.5 by +1–1.3 cm +, callus absent; appendages absent; bracteole pale brown to green, boat-shaped, +12–13 mm +long, callus absent; calyx pale brown to green, +9–20 mm +long, lobes (broadly) triangular, +1–4 mm +long, callus absent; corolla white to pale green, +28–35 mm +long, glabrous, tube +10–15 mm +long, lobes erect, narrowly ovate-triangular, +18–20 mm +long; labellum white to slightly pink, inner side with yellow or orange nectar guide in the throat, horizontally flattened, (broadly) obo- vate when spread out, 20–50 by +12–30 mm +, margin crenate; stamen white, 15–35 by (1.5–) +3–4 mm +, apex yellow, anther +2–3 mm +long; stigma is composed of a funnel-shaped upper part and a reflexed lamellate part; appendage absent. +Fruit +and +seeds +not seen. + + + + + + + + + + + + + + + + +
(
(
+ +
+Map 15 +Distribution of + +Paracostus englerianus +(K.Schum.) C.D.Specht. + +
+ +Distribution — West Africa (Benin, Ghana, Ivory Coast, Ni- geria); Central Africa (Cameroon, Congo Brazzaville, Equatorial Guinea, Gabon). + + + +Habitat & Ecology + +Understory of lowland rainforest, often forming dense patches and growing on rocks. At elevations of +0–1100 m +. Flowering and fruiting: all year through. + + + + +IUCN Conservation Status — + +Paracostus englerianus + +with around 50 locations of which 14 have a protected status and an AOO of +484 km +2 +is assessed by us as Least Concern ( +LC +). However, we need to note that nearly the entire distribution in Upper +Guinea +(West of the +Dahomey +Gap) is present in unprotected areas (only the locality in the Atewa Range has some protection, but see Hoekstra et al. 2016), while this area is seriously facing habitat destruction. If this somewhat isolated part of the species would prove to possess unique genetic (or morphological) features, these populations should get some attention and might need to be assessed separately. + + + + +Note — + +Paracostus englerianus + +is distinguished from other African + +Costaceae + +by its prostrate and often lithophilic habit, 1 solitary leaf per shoot, few-flowered inflorescence with inconspicuous bracts and relatively small whitish flowers. The inflorescence of + +P. englerianus + +is axillary. According to Specht & Stevenson (2006) the inflorescence emerges from the axil of the leaf and appears terminal due to secondary displacement along with lack of continued growth of the shoot apical meristem. + + +
+
\ No newline at end of file diff --git a/data/38/76/87/387687E2BB1EFFD5FC84FDCCFAEBFCC4.xml b/data/38/76/87/387687E2BB1EFFD5FC84FDCCFAEBFCC4.xml new file mode 100644 index 00000000000..f8ccbe7c784 --- /dev/null +++ b/data/38/76/87/387687E2BB1EFFD5FC84FDCCFAEBFCC4.xml @@ -0,0 +1,140 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + + +Paracostus + + + + + + + + +Paracostus +C.D.Specht + +in Specht & Stevenson (2006) 162. — Type: +Tafel 13 of K. Schumann (1892) +, (the +lectotype +of + +Costus englerianus +K.Schum. + +) + + + + + + +Costus + +L. sect. + +Paracostus +K.Schum. (1899) + +343. — + +Costus +subg. +Paracostus +(K.Schum.) K.Schum. (1904) + +381. — +Type +: + +Paracostus paradoxus +(K.Schum.) C.D.Specht + +(= + +Costus paradoxus +K.Schum. + +). + + + + +The genus + +Paracostus + +is in Africa represented by only one species: + +P. englerianus + +. The second species, + +P. paradoxus +(K.Schum.) C.D.Specht + +, occurs in Asia (Borneo). + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB1FFFD4FC84FD63FC2FFD78.xml b/data/38/76/87/387687E2BB1FFFD4FC84FD63FC2FFD78.xml new file mode 100644 index 00000000000..d4cfe923327 --- /dev/null +++ b/data/38/76/87/387687E2BB1FFFD4FC84FD63FC2FFD78.xml @@ -0,0 +1,88 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 + + + + + +Costus zechii +K.Schum. (1904) + +409. — + + + + + +Type +: +Zech auf Neuhofen 273c +(holo +B +destroyed), +Ghana +, +Kete Krachi +(‘ +bei Kete Kratschi’ +) + +. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB1FFFD4FC84FDDAFBAFFDE0.xml b/data/38/76/87/387687E2BB1FFFD4FC84FDDAFBAFFDE0.xml new file mode 100644 index 00000000000..e195a9661e6 --- /dev/null +++ b/data/38/76/87/387687E2BB1FFFD4FC84FDDAFBAFFDE0.xml @@ -0,0 +1,95 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 + + + + + +Costus ulugurensis +K.Schum. (1904) + +396. — + + + + + +Type +: +Stuhlmann 8709 +(holo +B +destroyed), +Tanzania +, +N’glewenu +, +Mo- huba +, + +350 m + +, + +17 Oct. 1894 + + +. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB1FFFD4FC84FE31FA8BFD89.xml b/data/38/76/87/387687E2BB1FFFD4FC84FE31FA8BFD89.xml new file mode 100644 index 00000000000..d352613a235 --- /dev/null +++ b/data/38/76/87/387687E2BB1FFFD4FC84FE31FA8BFD89.xml @@ -0,0 +1,93 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 + + + + + +Costus schlechteri +H.J.P.Winkl. (1908) + +275. — + + + + + +Type +: +Winkler 25a +(holo +B +destroyed), +Cameroon +, +South-West Province +, +Victoria +, ‘ +Urwald hinter dem Kirchhof’ +, + +May 1904 + + +. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB1FFFD4FC84FE8BFA17FE2E.xml b/data/38/76/87/387687E2BB1FFFD4FC84FE8BFA17FE2E.xml new file mode 100644 index 00000000000..727dee05098 --- /dev/null +++ b/data/38/76/87/387687E2BB1FFFD4FC84FE8BFA17FE2E.xml @@ -0,0 +1,78 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 + + + + + +Costus mosaicus +W.Bull (1887) + +10, ‘Congo’, nom. dub. + + + + +This might be a variegated form of an African species of + +Costus + +. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB1FFFD4FC84FEC6FA16FEF8.xml b/data/38/76/87/387687E2BB1FFFD4FC84FEC6FA16FEF8.xml new file mode 100644 index 00000000000..4e2c171cef3 --- /dev/null +++ b/data/38/76/87/387687E2BB1FFFD4FC84FEC6FA16FEF8.xml @@ -0,0 +1,87 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 + + + + + +Costus ledermannii +Loes. (1909) + +391. — + + + + + +Type +: +Ledermann 344 +(holo +B +destroyed), +Cameroon +, +South Province +, +Bodje + +. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB1FFFD4FC84FF5AFB00FE85.xml b/data/38/76/87/387687E2BB1FFFD4FC84FF5AFB00FE85.xml new file mode 100644 index 00000000000..7670ae4e5c5 --- /dev/null +++ b/data/38/76/87/387687E2BB1FFFD4FC84FF5AFB00FE85.xml @@ -0,0 +1,92 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 + + + + + +Costus dendrophilus +K.Schum. (1904) + +416. — + + + + + +Type +: +Dinklage 1138 +(holo +B +destroyed), +Cameroon +, +South Province +, +Batanga +, + +16 Feb. 1891 + +. This species has been described as being an epiphyte by Schumann + +. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB1FFFD4FFCDF82CFD29F7F9.xml b/data/38/76/87/387687E2BB1FFFD4FFCDF82CFD29F7F9.xml new file mode 100644 index 00000000000..c1f1a839266 --- /dev/null +++ b/data/38/76/87/387687E2BB1FFFD4FFCDF82CFD29F7F9.xml @@ -0,0 +1,87 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 + + + + + +Costus bicolor +J.Braun & K.Schum. (1889) + +152. — + + + + + +Type +: +Braun 91 +(holo +B +destroyed), +Cameroon +, ‘in +Múha +, bei Mal- +imba auf dicken Baümen in Inundationsgebiet des Sannaga flusses’ +. This epiphytic species is insufficiently understood because the type (and only material) in B has been destroyed + + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB1FFFD4FFCDF859FD70F85B.xml b/data/38/76/87/387687E2BB1FFFD4FFCDF859FD70F85B.xml new file mode 100644 index 00000000000..f766baeded6 --- /dev/null +++ b/data/38/76/87/387687E2BB1FFFD4FFCDF859FD70F85B.xml @@ -0,0 +1,69 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 + + + + + +Costus auriculatus +K.Schum. (1904) + +396, nom nud. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB1FFFD4FFCDF8DFFE62F809.xml b/data/38/76/87/387687E2BB1FFFD4FFCDF8DFFE62F809.xml new file mode 100644 index 00000000000..1c967e683dc --- /dev/null +++ b/data/38/76/87/387687E2BB1FFFD4FFCDF8DFFE62F809.xml @@ -0,0 +1,98 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 + + + + + +Costus adolphi-friderici +Loes. (1910) + +66 (as ‘ +Adolphi Friderici +’). — + + + + + +Type +: +Mildbraed 2378 +(holo +B +destroyed), +Congo Kinshasa +, +Nord-Kivu +, +Beni +, ‘ +Im Urwald bei Muera +, +nordwest- lich von Beni +, + +Januar 1908 + +’ + +. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB20FFEAFC84FCE2FDFEFA4E.xml b/data/38/76/87/387687E2BB20FFEAFC84FCE2FDFEFA4E.xml new file mode 100644 index 00000000000..aea0076e204 --- /dev/null +++ b/data/38/76/87/387687E2BB20FFEAFC84FCE2FDFEFA4E.xml @@ -0,0 +1,404 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +22. + +Costus spectabilis +(Fenzl) K.Schum. + + +— +Plate 4c +; +Map 13 + + + + + +Costus spectabilis +(Fenzl) K.Schum. (1892) + +422; (1904) 421. — + +Cadalvena spectabilis +Fenzl (1865) + +140. — + +Kaempferia spectabilis +(Fenzl) Baker (1898) + +297. — + +Type +: +Boriani s.n. +(holo +W +destroyed), +Sudan +, +Fazughli +(‘in Aethiopiae terra Fassoglu’). + +The following collection is selected here as + +neotype +: +Schweinfurth 1345 +(neo +BM +,designated here; + + +isoneo +G +, +K +, +L +, +P +), +Sudan +, +Gallabat +(‘Am linken Ufer der Gendua’), June 1865. A drawing in the B herbarium with annotation: ‘ + +18 Juni 1865 + +, +Ethiopia +, in +Gallabas +, an der Gendua’ is probably made of +Schweinfurth 1345 +, the present neotype of this species + +. + + + + + + +Costus pistiifolius +K.Schum.(1892) + +424. — + +Cadalvena pistiifolia +(K.Schum.) Baker (1898) + +297. — +Type +: +Von Mechow 315 +(holo +B +destroyed; + + +lecto +Z +, designated here), +Angola +, +Prov. Malanje +, +Malanje +(‘Malandsche’), + +Oct. 1879 + + +. + + + + +Cadalvena dalzielii +C.H.Wright (1912) + +195; C.H.Wright (1915) t. 3013, syn. nov. — +Type +: +Dalziel 229 +(lecto +K +, designated here), +Nigeria +, Yola Prov- ince, +Kilba Country +, + +30 July 1909 + +; + + +other +syntype +: +Dalziel 560 +( +K +2 +sheets, +E +2 +sheets), +Nigeria +, South of +Sokota Province +and throughout +Kontagora Province +, + +12 June 1911 + + +. + + + + +Terrestrial shootless rosulate herb to c. +0.1 m +tall; rhizomes vertically directed, to c. +18 cm +deep; horizontal runners to +5–20 cm +long, (1–) +3–9 mm +diam, both rhizomes and runners covered with brownish, imbricate, membranous sheaths; roots with side roots up to c. +10 cm +long. +Leaves +4 per shoot, forming a funnel when young, later spreading horizontally and forming a rosette of partly overlapping leaves flat on the ground; ligule and petiole absent; lamina bright yellowish green above, paler green with reddish venation to completely reddish below, often with (dark) reddish margins +0.5–1 mm +wide, definitively thick- ened and fleshy, imbricate, broadly obovate to broadly elliptic to suborbicular, 4–15(–17) by +4–17 cm +, upper side glabrous, lower side densely covered with soft, erect hairs < +1 mm +long, margin ciliate, base attenuate, extreme base of leaf fleshy to c. +5 mm +thick and +10–35 mm +long, at an angle of 90° with the lamina surrounding the inflorescence, apex obtuse and often mucronate. +Inflorescence +terminal, formed in the centre of the rosette, up to 17-flowered, basally enclosed by the more or less overlapping fleshy extreme base of the leaf laminas and by the uppermost 4–5 (whitish and fleshy) sheaths; sheaths 2–4 by +1.5–3.5 cm +, apex rounded, upper part reflexed with a horizontal rim of +0.7–0.8 cm +high, together forming a cup of +0.8–2.5 cm +diam around the inflorescence; the uppermost sheaths, outer side of bracts, bracteoles, calyx and apex of ovary densely to sparsely covered with soft, erect hairs < +1 mm +long to glabrous, capsule glabrous. +Flowers +1 per bract, erect; bracts reddish, membranous, narrowly triangular, 1.7–3.2 by +0.6–0.8 cm +, callus yellow, inconspicuous; appendages absent; bracteole boat-shaped, +8–25 mm +long, callus absent; calyx reddish, green, or purple, +15–30 mm +long, split on one side, lobes 2, narrowly triangular, c. +1 mm +long, callus inconspicuous; corolla hyaline, pale yellow to pale orange, +40–100 mm +long, glabrous, tube +20–45 mm +long, lobes narrowly ovate-triangular, +20–55 mm +long; labellum dark yellow to orange, horizontally flattened, obtriangular to obovate to suborbicular when spread out, 50–70 by +30–50 mm +, margin crenate; stamen orange to yellow, 15–40(–60) by +5–7 mm +, anther 4–7(–12) mm long. +Capsule +subterranean, ellipsoid, 6–12 by +4–7 mm +. +Seeds +c. 2 by +2 mm +. + + + + + + + + + + + + + + +
((
+ +
+Map 14 + +Distribution of + +Costus phyllocephalus +K.Schum. + +
+ +Distribution — North Africa (Egypt); North East Africa (Ethiopia, South Sudan, Sudan); West Africa (Benin, Burkina Faso, Ghana, Guinea, Guinea-Bissau, Ivory Coast, Mali, Niger, Ni- geria, Senegal, Sierra Leone, Togo); Central Africa (Burundi, Cameroon, Central African Republic, Chad, Congo Brazzaville, Congo Kinshasa, Gabon); East Africa (Kenya, Tanzania, Ugan- da); Southern Tropical Africa (Angola, Malawi, Mozambique, Zambia, Zimbabwe). + + + +Habitat & Ecology — Often in savanna woodland (with e.g. +Brachystegiae +, +Primary +, etc.), on clayey to loamy soil, or on rocky outcrops, often on ant hills, at elevations of +0–2000 m +. Flowering and fruiting: April to December, mostly in October and December. + + + + +Field observations — Completely leafless flowering specimens have been collected in May– June and October–De- cember. Information on the labels of +Michel & Reed 70 +and +Schlieben 1560 +mentions the appearance of + +C. spectabilis + +soon after burning. + + + +IUCN Conservation Status — Least Concern. + + + +Notes — + +Costus spectabilis + +can be recognized by its four horizontally spreading leaves forming a cruciform rosette flat on the ground, with an inflorescence in the centre producing large yellow flowers. For morphological differences between + +C. spectabilis + +and the only other shootless rosulate species + +C. macranthus + +see under the latter. Both + +C. spectabilis + +and + +C. macranthus + +occur in the region between E28–35° and S6–15° in +Malawi +, +Mozambique +, +Tanzania +, +Uganda +, +Zambia +and +Zimbabwe +.All collections of + +C. spectabilis + +have been found in an area where + +C. macranthus + +has also been collected. However, + +C. spectabilis + +has been collected in a much wider area than + +C. macranthus + +: between +W13° +– +E33° +and +N12° +– +S15° +and therefore in more countries, especially in Western Africa (see map 1 of Lock 1984). + + +
+
\ No newline at end of file diff --git a/data/38/76/87/387687E2BB21FFD5FC84F876FB37FD8E.xml b/data/38/76/87/387687E2BB21FFD5FC84F876FB37FD8E.xml new file mode 100644 index 00000000000..bd4aa60cf1e --- /dev/null +++ b/data/38/76/87/387687E2BB21FFD5FC84F876FB37FD8E.xml @@ -0,0 +1,456 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +24. + +Costus tappenbeckianus +J.Braun & K.Schum. + + +— +Plate 3c +; +Map 10 + + + + + + +Costus tappenbeckianus +J.Braun & K.Schum. (1889) + +152; K.Schum. (1904) 416. — +Type +: +Braun s.n +. (holo +B +destroyed), cultivated and flowering in + + +April +1889 in + + +the +Hort. Bot. +Berlin +from material collected in Gross-Batanga, +South Province +,Cameroon.As the holotype in +Berlin +was destroyed and no other type material was located, + + +we hereby select a +neotype +from a locality not far from the type locality: +J.J.F.E. de Wilde 8702 +(neo +WAG +2 +sheets [ +WAG0114484 +, +WAG0114485 +]; + + +isoneo +BR +, +EA +, +K +, +MA +, +MO +, +P +, +PRE +, +YA +), Cameroon, +South-West Province +, +Dipikar Island +, + +3 km +SE of the bridge crossing the Bongola River + +, along forest exploitation track, + +3 Dec. 1975 + + +. + + + + + + +Costus pauciflorus +K.Schum. (1892) + +421, syn. nov. — +Type +: +Soyaux 119 +(holo +B +destroyed; + + +lecto +K +, designated here), +Gabon +, +Estuaire +, ‘ +in ditione Munda, Sibange-Farm’ +, + +3 Sept. 1880 + + +. + + + + +Costus radicans +Gagnep. (1903) + +262, syn. nov. — +Type +: +Bates 519 +(holo +P +; + + +iso +BM +, +G +, +K +), +Gabon +, +Estuaire +, +Mfôa +, + +85 miles +E of Gaboon + +, + +Oct. 1896 + + +. + + + + +Costus nemotrichus +K.Schum. (1904) + +414,f. 47,syn. nov. — +Type +: +Dinklage 954 +(holo +B +destroyed), +Cameroon +, +South Province +, +Gross-Batanga + +. + + + + +Costus phaeotrichus +Loes. (1909) + +392, syn. nov. — +Type +: +Zenker 3694 +( +B +destroyed; + + +lecto +P +, designated here; + + +isolecto +BM +, +E +, +G +, +K +, +L +, +M +, +P +, +S +, +US +, +W +), +Cameroon +, +South Province +, +Bipindi +(‘Bipindihof’), ‘blühend vom Dezember bis Februar,1908’; + + +other +syntype +: +Ledermann 945 +( +B +destroyed), +Cameroon +, +South Province +, +Mfosse +, +near Nkolebunde +, + +180 m + + +, + + + + +Terrestrial herb +0.2–1 m +tall. +Leaves +several; sheaths brownish red, shiny, more or less turbinate, +0.3–1 cm +diam, upper margin irregularly denticulate; ligule chartaceous, truncate, +1–5 mm +long; petiole +0–3 mm +long; sheaths, ligule and petiole densely to sparsely covered with half-appressed to erect, brown, needlelike hairs to c. +4 mm +long to glabrous; lamina often irregularly bullate and 5–10-plicate ( +Maas 9962 +), upper side shiny, bright green, lower side reddish to purplish, elliptic to obovate, often slightly asymmetrical, 5.5–18(–22) by 2.5–7(–14) cm, both sides rather densely to sparsely covered with half-appressed to erect, brown, needle-like hairs to c. +4 mm +long to glabrous, base cordate, apex acute to acuminate (acumen to c. +10 mm +long). +Inflorescence +few-flowered, (narrowly) ovoid to ellipsoid, 2.5–4 by +1–1.5 cm +, terminating a separate leafless shoot +1–9 cm +long, or rarely terminating a leafy shoot; bracts, bracteoles, calyx, ovary and capsule glabrous or nearly so. +Flowers +2 per bract; bracts brownish red to dark purple, shiny, chartaceous, ovate-triangular, 2–3.5 by +0.7–3 cm +, callus brown, +2–4 mm +long; appendages absent; bracteole boat-shaped, +22–35 mm +long, callus green to yellow, c. +2 mm +long; calyx (5–) +10–13 mm +long, lobes broadly triangular, +1–2 mm +long, callus absent; corolla hyaline, whitish pink, +55–90 mm +long, glabrous, tube +15–30 mm +long, lobes narrowly elliptic, +30–60 mm +long; label- lum at the outer side white with dark pink upper half, inner side with white throat, dark pink upper part, or completely dark pink, or rarely completely white, with yellow nectar guide, funnelshaped to horizontally flattened, broadly obovate when spread out, 35–70 by +40–60 mm +, margin undulate and fimbriate; stamen white to pink, 20–45 by +9–12 mm +, apex pink to red, anther +5–6 mm +long. +Capsule +broadly obovoid, c. 8 by +7 mm +. +Seeds +2–3 by +3–4 mm +. + + + +Distribution — Central Africa (Cabinda (Angola), Cameroon, Congo Brazzaville, Equatorial Guinea, Gabon). + + + +Habitat & Ecology — In non-inundated primary or second- ary rainforest, in swamp forest, in dark wet places, on loamy or sandy soil. At elevations of + +0– +800 m. + +Flowering and fruiting: all year through. + + + +IUCN Conservation Status — Least Concern. + + + +Notes — + +Costus tappenbeckianus + +is characterized by a fewflowered inflorescence terminating a separate leafless shoot with pink (or rarely white) flowers and subsessile leaves with a cordate base. The sheaths, especially those of the separate reproductive leafless shoot, are more or less turbinate with an irregularly denticulate reddish upper margin. The corolla lobes are relatively narrow. Left and right margin of the labellum are not touching each other, thus not forming a complete funnel. A specimen with white flowers is cultivated in Burgers’ Bush, Arnhem, The Netherlands; it was originally collected in Gabon ( +Maas & Maas 9787 +). + +Costus tappenbeckianus + +was placed by Schumann (1904: 414) in his new subg. +Epicostus +together with + +C. bicolor +, +C. dendrophilus +, +C. lanceolatus +, +C. nemotrichus +, +C. nudicaulis +, +C. pauciflorus + +and + +C. radicans + +. According to him these species were all epiphytic (‘saepissime epiphytici’), except for + +C. tappenbeckianus + +, had a small and few-flowered inflorescence and nicely coloured, but never yellow, flowers. + +Costus nudicaulis + +(now in- cluded in + +C. phyllocephalus + +) and the Neotropical species + +C. lanceolatus + +were different from the other six species of this sub- genus by an inflorescence terminating a leafy shoot. After an intensive study of the six other species of the subg. +Epicostus +with an inflorescence terminating a separate leafless shoot, we found that they only differed in minor indument features. + +Costus bicolor + +and + +C. dendrophilus +, + +of which no material is available (as that has been destroyed) are here considered insufficiently known species (see below) + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB21FFEAFFCDF9F3FA16F8D0.xml b/data/38/76/87/387687E2BB21FFEAFFCDF9F3FA16F8D0.xml new file mode 100644 index 00000000000..13ba4cfb3b7 --- /dev/null +++ b/data/38/76/87/387687E2BB21FFEAFFCDF9F3FA16F8D0.xml @@ -0,0 +1,289 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +23. + +Costus talbotii +Ridl. + + +— +Plate 4e +; +Map 9 + + + + + + +Costus talbotii +Ridl. (1913) + +111. — +Type +: +Talbot 1521 +(lecto +BM +2 +sheets, designated by Turner (2000); + + +isolecto +K +), +Nigeria +, +Cross River +State +, +Oban +, anno 1912 + +. + + + + +Epiphytic or terrestrial herb c. +0.5 m +tall. +Leaves +several; sheaths +0.2–0.5 cm +diam; ligule brown, membranous, truncate, +40–55 mm +long; petiole +3–10 mm +long; sheaths, ligule and petiole glabrous; lamina narrowly elliptic, 10–18 by +3–5 cm +, glabrous on both sides, coriaceous and somewhat fleshy, base obtuse to acute, apex acuminate (acumen +10–20 mm +long). +Inflorescence +few-flowered, broadly ovoid, 2–3 by +1.5–2.5 cm +, terminating a separate leafless shoot < +1 cm +long, lateral in the axil of a leaf, or rarely terminal, sheaths dark brown, broadly to transversely elliptic, 6–14 by +9–15 mm +; bracts sparsely to rather densely covered with appressed hairs < +1 mm +long, bracteoles, ovary and capsule rather densely covered with erect hairs < +1 mm +long, calyx glabrous or sparsely covered with appressed to erect hairs < +1 mm +long. +Flowers +2 per bract; bracts reddish brown to dark brown, coriaceous, broadly ovate-triangular, 1.2–2 by +1.3–2 cm +, callus absent or sometimes present and c. +0.5 mm +long; appendages absent; bracteole boat-shaped, +15–20 mm +long, callus green, +1–2 mm +long; calyx green, dark reddish dotted, +11–15 mm +long, lobes broadly to shallowly triangular, +2–4 mm +, callus +1–2 mm +long; corolla tube white, lobes hyaline, dark pink, +35–40 mm +long, glabrous, tube c. +10 mm +long, lobes narrowly elliptic, +25–30 mm +long; labellum white on the outer side, inner side white to dark pink with pink dots in the throat and yellow nectar guide, horizontally flattened, broadly obovate when spread out, 30–40 by +30–40 mm +, margin indistinctly ir- regularly 5-lobed, crenate; stamen white with pink dots, c. 25 by +8–9 mm +, apex pink, 3-lobed, lobes linear, middle lobe longer than the lateral ones, anther +5–6 mm +long. +Capsule +ovoid to broadly ovoid, 9–15 by +7–9 mm +. +Seeds +2–2.5 by +1 mm +. + + + +Distribution — West Africa (Nigeria, near the border with Cameroon). At unknown elevations. + + +Habitat & Ecology — Unknown. Flowering and fruiting: unknown. + + + +IUCN Conservation Status — + +Costus talbotii + +was collected as a herbarium specimen twice in the wild, both collections were made in the same area over 100 years ago without precise locality information (one location, +AOO +of 4 or +8 km +2 +). However, since it apparently was collected more recently (1978) for cultivation in a botanical garden, we do not consider this species as Extinct in the Wild. The area where it was collected ( +SE +Nigeria +) is poorly explored over the past 40 years, so it is not a surprise there are no recent collections: on the other hand it was not collected in the decades before that (or only once as living plant) when there was more botanical activity in the region. In this area there are extensive protected areas present, but satellite images show there is also logging, cultivation and mining going on in the area, including in some of the protected areas. So it seems at least part of this area is under serious threat for habitat destruction. We therefore assess the species as Critically Endangered ( +CR +) B2a(iii,v). + + + + +Notes — + +Costus talbotii + +is distinct from the two other epiphytic African species of + +Costus + +by its much broader (to c. +2 cm +wide) coriaceous bracts vs the chartaceous bracts (to +1.1 cm +wide) in + +C. lateriflorus + +and + +C. lilaceus +. + +Moreover, the flower colour of the three species is clearly different. + +Costus talbotii + +is a very incompletely known species: it is only known from the +type +collection and from cultivation. This plant has been cultivated at the +Cambridge +Botanical Garden in +England +under the accession number 19780014. It had been collected in Oban, +Cross River +State, +Nigeria +(the +type +local- ity) in 1978, where it was gathered by P.W. Richards, then Professor at the Cambridge University. This material died in the +Cambridge +Botanical Garden in 1996. Luckily living material had been sent to the Delft Botanical Garden in +The Netherlands +where it is still cultivated under the number Delft 46-490. From Delft some living plants were sent to Burgers’ Zoo in Arnhem ( +The Netherlands +), where it is now grown under the number Burgers’ Bush 2008-0109009. The plant flowered in 2009 and was photographed, described and collected by the second author ( +Maas et al. 9800 +). + +Of the +two +syntypes +of + +C. talbotii +, +Zenker 3823 + +( +BM +, +E +, +G +, +K +, +US +, +WRSL +), anno 1909, from +Bipindi +, Cameroon does not rep- resent + +C. talbotii + +but belongs to + +C. lateriflorus + +or to + +C. lilaceus +. + + + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB22FFE8FFCDFB19FDEBFC9C.xml b/data/38/76/87/387687E2BB22FFE8FFCDFB19FDEBFC9C.xml new file mode 100644 index 00000000000..2b178a29f9a --- /dev/null +++ b/data/38/76/87/387687E2BB22FFE8FFCDFB19FDEBFC9C.xml @@ -0,0 +1,257 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +19. + +Costus macranthus +K.Schum. + + +— +Plate 4a +; +Map 13 + + + + + + +Costus macranthus +K.Schum.(1901) + +279, t. 7, 8; (1904) 421 — +Type +: +Goetze 1488 +(holo +B +destroyed; + + +lecto +E +, designated here; isolecto +BM +, +BR +, +EA +), +Tanzania +, T7, ‘ +Rungwe District +, +Kondeland +, im +Kivirithal +, am +Kasimulo hügel im Buschwald +bei 600 m’, + +Nov. 1899 + + +. + + + + +Terrestrial shootless rosulate herb +0.1–0.2 m +tall; rhizomes vertically directed, to c. +10 cm +deep; horizontal runners to c. +40 cm +long, 3–5(–7) mm diam, both rhizomes and runners covered with pale brown, membranous, imbricate sheaths +1.3–2 cm +long; roots with side roots to c. +13 cm +long. +Leaves +(3–)4(–5) per shoot, spreading horizontally and forming a cruciform rosette flat on the ground; ligule rarely seen, c. +0.5 mm +long; petiole absent; lamina pale to yellowish green above, greenish purple below, with hyaline, red-purple to pink margins < +1 mm +wide, distinctly thickened and fleshy, elliptic, broadly elliptic, obovate, or suborbicular, 7–20(–30) by 5–22(–25) cm, upper side glabrous to rather densely covered with soft erect hairs < +1 mm +long, lower side glabrous to rather densely, rarely densely, covered with soft, erect hairs < +1 mm +long, margin densely ciliate, base acute, extreme base of leaf +20–30 mm +long, at an angle of 90° with the lamina, surrounding the inflo- rescence, apex obtuse and mucronate (mucro c. +1 mm +long). +Inflorescence +terminal, formed in the centre of the rosette, few-flowered, basally enclosed by the more or less overlapping thickened extreme base of the leaves and by the uppermost 4–6 sheaths; sheaths 2–6.5 by +1–6 cm +, apex obtuse to round- ed, together forming a cup of +1–3 cm +diam around the inflo- rescence; upper part of uppermost sheaths rather densely covered with soft erect hairs < +1 mm +long with thickened base; upper part of bracts, bracteoles, calyx and ovary rather densely covered with soft erect hairs < +1 mm +long, capsule glabrous. +Flowers +1 per bract; bracts whitish green, membranous, nar- rowly ovate-triangular, 1.7–4 by +0.4–0.8 cm +, callus absent; appendages absent; bracteole boat-shaped, c. +15 mm +long, callus absent; calyx +35–75 mm +long, split on one side, lobes 2, broadly triangular, +2–5 mm +long, callus absent; corolla (pale) yellow, +90–130 mm +long, glabrous, tube +50–90 mm +long, lobes narrowly ovate-triangular, +40–80 mm +long; labellum bright yel- low to orange, horizontally flattened, basally funnel-shaped, obovate to suborbicular when spread out, 70–110 by +60–110 mm +, margin crenate; stamen yellow, 60–80 by +7–10 mm +, anther (6–)7–12(–15) mm long. +Capsule +subterranean, subglobose, c. 10 by +9 mm +. +Seeds +not seen. + + + +Distribution — East Africa (Tanzania, Uganda); Southern Tropical Africa (Malawi, Mozambique, Zambia, Zimbabwe). + + + +Habitat & Ecology — In non-inundated forest, open grass land, often on steep, rocky soil, sometimes around ant hills, plants growing in colonies, locally common, at elevations of (250–) +500–1700 m +. Flowering and fruiting: November and December and rarely from January to March. + + + +IUCN Conservation Status — Least Concern. + + + +Notes — + +Costus macranthus + +can be recognized by four horizontally spreading leaves forming a cruciform rosette flat on the ground and a central inflorescence producing large yellow flowers, in this aspect very much resembling + +C. spectabilis + +. Lock (1984) differentiates the two species based on the length of several flower parts. Of these, the length of the anther is the most reliable in herbarium material. In + +C. macranthus + +the anther is (6–)7–12(–15) mm long (we recorded a length of +10 mm +for +15 specimens +studied) and in + +C. spectabilis + +4–7(–12) mm long (we recorded +5 mm +for a total of +17 specimens +). Among other distinguishing characters are the length of calyx, corolla tube, corolla lobes and labellum. These are all larger in + +C. macranthus + +than in + +C. spectabilis + +. Many other possible distinctive characters still have to be studied in the field, e.g. difference in flower colour, time of floral and vegetative development (if flowers emerge before leaf emergence, at the same time as leaf development, or after leaf dehiscence) and morphology of the underground parts. Both + +C. macranthus + +and + +C. spectabilis + +occur in the region between E28–35° and S6–15° in Malawi, Mozambique, Tanzania, Uganda, Zambia and Zimbabwe. All collections of + +C. macranthus + +have been found in an area where + +C. spectabilis + +has also been collected. In this area the majority of the (c. 50) herbarium specimens of both species available for this study were collected flowering in November to December. Both species were found between 500 and +2000 m +altitude. In this geographic range, at this altitude and with flower, specimens of both species were collected either with very young leaves or with senescent leaves. For + +C. macranthus + +we also recorded +5 specimens +collected without any leaves. Lock wrote in Flora Zambesiaca (Lock & Diniz 2010: 117): “Inflorescence developing with the leaves or just before, but flowering continu- ing until leaves are almost fully developed”. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB23FFE8FFCDFCC7FC07FB31.xml b/data/38/76/87/387687E2BB23FFE8FFCDFCC7FC07FB31.xml new file mode 100644 index 00000000000..e10c32f68ca --- /dev/null +++ b/data/38/76/87/387687E2BB23FFE8FFCDFCC7FC07FB31.xml @@ -0,0 +1,583 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +20. + +Costus nimba +H.Maas & Maas + + +, + +sp. nov. + +— +Plate 4b, d +; +Map 12 + + + + + +Costus nimba + +is characterized by the dense brown indument of its vegeta- tive parts, an inflorescence on a relatively long separate leafless shoot, green bracts and white to salmon pink flowers with a horizontally flattened labellum. — + + + + + +Type +: +Phillipson 6415 +(holo +WAG +2 +sheets; + + +iso +MO +, +P +), +Guinea +, +Nzérékoré +, +Nimba Mountains +, lower +Zié Valley +, at edge of +World Heritage Site +, +along river bank in sandy soil +, + +591 m + +, + +10 July 2012 + + +. + + + + +Terrestrial herb +1.5–2.5 m +tall. +Leaves +many; sheaths, +0.8–2.5 cm +diam; ligule chartaceous, obliquely truncate to slightly unequally 2-lobed, +14–23 mm +long; petiole +13–33 mm +long; sheaths, ligule and petiole densely to very densely covered with erect, brown hairs +1–2 mm +long; lamina chartaceous, narrowly obovate to narrowly elliptic, 24–36 by +6–10 cm +, upper side glabrous except for the midrib, lower side and midrib on upper side (very) densely covered with appressed hairs +1–1.5 mm +long, base acute, apex acute to acuminate (acumen +15–20 mm +long). +Inflorescence +many-flowered, ovoid-ellipsoid to cylindric, 10–17 by +4–5.5 cm +, terminating the leafy shoot or terminating a separate leafless shoot +24–30 cm +long; bracts, bracteoles, calyx, ovary and capsule glabrous. +Flowers +1 per bract; bracts green, coriaceous, broadly ovate, 3–3.5 by +2.5–3.5 cm +, callus indistinct; appendages absent; bracteole boat-shaped, +30–35 mm +long, callus present, +2–4 mm +long; calyx +18–22 mm +long, lobes broadly ovate-triangular, +4–6 mm +long, callus +1–2 mm +long; corolla hyaline, salmon-coloured, +40–60 mm +long, gla- brous, tube +15–20 mm +long, lobes narrowly obovate-elliptic, 25–35(–40) long; labellum at the outer side white, inner side white to very pale salmon pink with pale yellow nectar guide and two dark pink basal zones covered with erect hairs c. +1.5 mm +long, horizontally flattened, depressed obovate when spread out, 40–45 by +40–45 mm +, margin crenulate; stamen white, c. 30 by +12–18 mm +, anther +7–8 mm +long, apex acute. +Capsule +ellipsoid to obovoid, 14–17 by +8–11 mm +. +Seeds +c. 2 by +1 mm +. + + + +Distribution — West Africa (Ghana, Guinea, Ivory Coast, Liberia, Sierra Leone); Central Africa (Cameroon). + + + +Habitat & Ecology — In rain +f +orest along river bank, in sandy soil, at elevations of +0–1150 m +. Flowering and fruiting: May to December. + + + + +Field observations — The flowers of + +C. nimba + +emit a ‘fragile sweet scent’ ( +Jongkind & Bilivogui 11301 +). + + + +IUCN Conservation Status — Least Concern. + + + + +Additional specimens examined. +CAMEROON +, + +South Province + +, Djoum, +600 m +, anno 2014, +Cheek 17660 +( +K +, +WAG +, +YA +) + +. + + +South-West Province + +, Mondemba-Fabe Road, +22 Nov. 1986 +, +Nemba & Thomas 331 +( +K +, +WAG +). – + + + + +GHANA +, + +Brong-Ahafo Region + +, between Wenchi and Bamboi, +350 m +, +3 Oct. 1996 + +, + + +Jongkind +3138 + +( +WAG +) + +. + + +Eastern Region + +, Kade, +2 June 1968 +, +Hall GC 38519 +( +GC +, +K +) + +; + +Busoso-Begoso Road, +16 June 1969 +, +Hossain & Enti GC 35403 +( +GC +) + +; + +‘Ex Garden Legon, original from Kade’, +18 Dec. 1956 +, +Morton GC 8334 = P 2051 +( +GC +) + +; + +Kwahu West District +,Akoase, +196 m +, +8 July 2010 +, + +Van Andel +et al. 5735 + +( +WAG +) + +. + + +GUINEA +, +Nzérékoré +, +Nimba Mts +, Zié Valley, +590 m +, +21 Sept. 2011 +, +Jongkind & Bilivogui 11163A +( +WAG +) + +; + +Nimba Mts +, Zié River, +667 m +, +10 July 2012 +, +Jongkind & Bilivogui 11301 +( +BRLU +, +WAG +) + +; + +Nimba Mts +, inside the WHS site close to the Zié River bridge, +540 m +, +28 Oct. 2012 + +, + + +Jongkind +et al. 11620 + +( +WAG +) + +. + + +IVORY COAST +, + +Divo + +, between + + +Divo +and Lakota, +18 Apr. 1968 +, +Aké Assi 10030 +( +G +) + +; + +Divo +, +5 km +SE of Guitry, +20 m +, +1 Nov. 1975 +, +Beentje 1283 +( +WAG +) + +; + +Forêt de + + +Divo +, +10 Aug. 1975 +, +Hall & Abbiw GC 45357 +( +GC +) + +. + +Guiglo + +, + +Taí +, between Sakré and Nigré, +28 Dec. 1987 +, +Aké Assi 17871 +( +G +) + +. + + +Man + + +, + +Man +, near climatic station on Mt Tonkoui, +1150 m +, +28 May 1975 +, +Beentje 341 +( +WAG +) + +. + +Soubré +, Haut +Sassandra +, Pays des Byolas, entrée du village de Dyedeougou, +10 May 1909 +, +Chevalier 21517 +( +P +) + +. + + +LIBERIA +, + +Eastern Province + + +, + +Webo District +,Sarbo, +6 July 1947 +, +Baldwin Jr. 6410a! +( +K +) + +. + + +SIERRA LEONE +, + +Northern Province + +, +15 miles +N of Port Loko, in garden at FBC, +28 Apr. 1965 +, +Morton s.n. +( +K +) + +. + + +Southern Province + +, near Mokebi (Kori), +26 May 1953 + +, + + +Jordan +900 + +( +K +) + +; + +without location, 1915, +Thomas 8455 +( +K +) + +. + + + + +Notes — + +Costus nimba + +comes closest to + +C. dubius + +, both sharing a basal inflorescence with green, unappendaged bracts. It differs, however, by the dense brown indument of its vegetative parts (absent in + +C. dubius + +), its horizontally flattened labellum with two basal salmon pink patches and yellow nectar guide (funnel-shaped with yellow nectar guide in + +C. dubius + +) and its hyaline salmon pink corolla lobes (white and not hyaline in + +C. dubius + +). + +Costus nimba + +differs from + +C. dinklagei +, + +another species having a basal inflorescence with green, unappendaged bracts and hyaline corolla lobes by its salmon pink corolla lobes (whitish in + +C. dinklagei + +), by its horizontally flattened white labellum with two basal salmon pink patches and yellow nectar guide (pale pink, funnel-shaped with yellow nectar guide in + +C. dinklagei + +) and its generally larger inflorescence and a longer separate leafless shoot. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB23FFEBFC84FB2CFA6AFD78.xml b/data/38/76/87/387687E2BB23FFEBFC84FB2CFA6AFD78.xml new file mode 100644 index 00000000000..b2e91498217 --- /dev/null +++ b/data/38/76/87/387687E2BB23FFEBFC84FB2CFA6AFD78.xml @@ -0,0 +1,458 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +6c0dbc52-820c-4f68-912d-1bcaa2227efc +7570023 + + + + + +21. + +Costus phyllocephalus +K.Schum. + + +— +Plate 3e +; +Map 14 + + + + + + +Costus phyllocephalus +K.Schum. (1892) + +420; (1904) 386. — +Type +: +Von Mechow 508 +(holo +B +destroyed; + + +lecto +Z +, designated here; + + +iso +M +), +Angola +, +Prov. Malanje +, +Malanje +(‘Malane’), +Quango River +, + +June–Aug. 1880 + + +. + + + + + +Costus nudicaulis +Baker +(1898) + +300, syn. nov. — + +Type +: +Mann 1033 +(holo +K +), +Gabon +, +Estuaire +, +Gaboon River +, + +July 1861 + + +. + + + +Costus dewevrei +De Wild. & T.Durand + +in Durand & De Wildeman (1899) 139, syn. nov. — + +Type +: +Dewèvre 334 +(holo +BR +; + + +iso +BR +), +Congo Kinshasa +, +Kinganga +(‘Chinganga’), + +29 Aug. 1895 + + +. + + + + +Costus fissiligulatus +Gagnep.(1902a) + +93,syn. nov. — +Type +: + +A plant cultivated at +Bot. Gard +. +Paris +as ‘Gabon Nº 639’, + + +July 1902 + +(holo +P +; + + +iso +P +) + +. + + + + +Costus fissiligulatus +Gagnep. var. +major +Gagnep. (1902a) + +94, syn. nov. — +Type +: +Griffon du Bellay s.n. +(holo +P +), +Gabon +, without locality, ‘ +Donné par l’Exposition Coloniale. Cat. 1864 Nº. 4 +’ + +. + + + + +Costus ubangiensis +Gagnep. (1902a) + +97, syn. nov. — +Type +: +Viancin s.n. +(holo +P +), +Central African Republic +, ‘ +Haut-Oubangui’ + +. + + + + +Costus nudicaulis +Baker var. +pilosa +Gagnep. (1902b) + +19, syn. nov. — +Type +: +Lecomte B25 +(holo +P +), +Congo Brazzaville +, ‘Nounzi’, + +Oct. 1893 + + +. + + + + +Costus violaceus +Koechlin (1964) + +88,pl. 20,syn.nov. — +Type +: +N. Hallé 1543 +(holo +P +), +Gabon +, +Ogooué-Maritime +, +Port-Gentil +, + +2 Apr. 1959 + + +. + + + + +Costus foliaceus +Lock & A.D.Poulsen + +in Poulsen & Lock (1997) 614, f. 3, pl. 2a, syn. nov. — +Type +: +Poulsen et al. 503 +(holo +K +; + + +iso +C +, +ENT +, +MHU +), +Uganda +, +Bushenyi District +, +Kasyoha-Kitomi +Forest Reserve +, +NE of Kyam- bura River +, + +1250 m + +, + +4 June 1994 + + +. + + + +Costus sp. A + +Lock & Diniz (2010) 120. + + + + +Terrestrial herb +0.2–3 m +tall. +Leaves +many; sheaths +0.5–2 cm +diam; ligule brown, upper margin reddish, membranous, split into 2 very unequal obtuse to acute lobes, +10–50 mm +long; petiole +3–10 mm +long; sheaths, ligule and petiole sparsely to densely covered with erect, brown hairs to c. +3 mm +long; lamina green to purple below, rarely red on both sides, narrowly ovate to narrowly obovate, 10–31 by +4–12 cm +, upper side glabrous or rarely sparsely to densely covered with erect hairs to c. +3 mm +long, lower side rather densely to sparsely covered with erect brown hairs to c. +3 mm +long to glabrous, base obtuse, rarely subcordate, apex acuminate (acumen +15–25 mm +long). +Inflorescence +(few- to) many-flowered, ovoid to globose, 2.5–10 by +3–7 cm +, terminating the leafy shoot, sometimes sprouting from the axils of the lower bracts; bracts, appendages of bracts, bracteoles, calyx, ovary and capsule sparsely to densely cov- ered with erect hairs < +1 mm +long to glabrous. +Flowers +1 per bract; bracts green to reddish purple, coriaceous, ovate-elliptic to broadly so, 1–2.5 by +1–2.5 cm +, callus sometimes present and then +1–2 mm +long; appendages mostly present, green, horizontally spreading to reflexed or rarely erect, narrowly tri- angular to rarely broadly ovate-triangular, 1–4.5(–6.5) by +5–20 cm +; bracteole boat-shaped, 1(–2)-keeled, +11–21 mm +long, cal- lus +2–3.5 mm +long; calyx +10–27 mm +long, lobes shallowly to broadly triangular, +2–4 mm +long, callus absent; corolla white to pale pink to lilac, +40–65 mm +long, glabrous, rarely covered with erect hairs < +1 mm +long, tube +10–20 mm +long, lobes narrowly obovate to narrowly elliptic, +30–55 mm +long; labellum white to pale pink on the outer side, inner side white with the upper half striped dark pink to lilac to dark purplish pink, or completely white to very pale pink, with yellow nectar guide, horizontally flattened, broadly obovate when spread out, 40–70 by +50–70 mm +, fimbriate, margin crenulate and/or undulate, sometimes 5-lobed; stamen white to yellow or dark pink, 30–45 by +10–15 mm +, apex yellow, tip of apex pink or pale yellow, toothed, anther +7–9 mm +long. +Capsule +subglobose to obovoid, 6–15 by +6–15 mm +. +Seeds +2–3 by +1–1.5 mm +. + + + +Distribution — West Africa (Nigeria); Central Africa (Burundi, Cameroon, Central African Republic, Congo Brazzaville, Congo Kinshasa, Gabon); East Africa (Uganda); Southern Tropical Africa (Angola, Zambia). + + + +Habitat & Ecology — In primary or secondary rainforest, gallery forest, sometimes in coastal forest or in wet places near savannas, rivers or creeks, or along roads, at elevations of +0–1500 m +. Flowering and fruiting: all year through. + + + + +Field observations — On the label of the specimen +Le Testu 2374 +is written ‘fleurs très odorantes’. + + + +IUCN Conservation Status — Least Concern. + + + +Notes — + +Costus phyllocephalus + +can be recognized by a combination of green appendaged bracts, leaves on flowering shoot concentrated just below the inflorescence, flowers of which the horizontally flattened labellum is whitish pink to striped with dark purplish pink and a long brown membranous ligule ( +10–50 mm +long). The upper brown membranous part of this ligule can be deciduous only leaving the lower green tubular part. + +Costus phyllocephalus + +looks quite similar to + +C. ligularis + +. For the differences between both species see under the latter. In + +C. phyllocephalus + +young shoots are sometimes formed from the lower bracts; these shoots have relative small ligules. In the fruiting stage the calyx is often protruding beyond the bracts. Some collections are aberrant from typical + +C. phyllocephalus + +in having unappendaged bracts. Sometimes there are transitions between the uppermost leaves and the appendages of the lowest bracts. The shoots are reddish and the leaves tend to be concentrated at the top of the shoot. The yellow central blotch (nectar guide) is situated in the throat of the flower and does not reach the outer margin of the labellum as in + +C. lucanusianus +. + + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB25FFE9FC84FCFCFD29FB5C.xml b/data/38/76/87/387687E2BB25FFE9FC84FCFCFD29FB5C.xml new file mode 100644 index 00000000000..f61fc6879ed --- /dev/null +++ b/data/38/76/87/387687E2BB25FFE9FC84FCFCFD29FB5C.xml @@ -0,0 +1,269 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +18. + +Costus maboumiensis +Pellegr. + + +— +Plate 3f +; +Map 12 + + + + + + +Costus maboumiensis +Pellegr. (1929) + +220. — +Type +: +Le Testu 1820 +(holo +P +; + + +iso +BM +2 sheets, +BR +, +MO +, +P +2 +sheets), +Gabon +, +Nyanga +, +Tchibanga +area, ‘ +Mayombe bavili, campement de la Maboumi’ +, + +27 Oct. 1914 + + +. + + + + +Terrestrial herb +1–2.6 m +tall. +Leaves +many; sheaths +0.7–2 cm +diam; shoots reddish, sheaths green with reddish margin, ligule chartaceous, truncate to 2-lobed, +5–20 mm +long; petiole +2–10 mm +long, tinged with reddish brown; sheaths, ligule and petiole glabrous; lamina narrowly elliptic, sometimes narrowly obovate, 15–30 by +5–10.5 cm +, glabrous on both sides, base acute, the very base sometimes obtuse to cordate, apex acuminate (acu- men +15–40 mm +long). +Inflorescence +many-flowered, ovoid to subglobose, 4–10 by +3–4.5 cm +, terminating a separate leafless shoot +20–50 cm +long; bracts, appendages of bracts, bracteoles, calyx and ovary glabrous. +Flowers +1 per bract; bracts somewhat bulging, pale to bright green, sometimes with narrow dark red margin, coriaceous, ovate to broadly ovate, 2–2.5 by +1–2 cm +, callus green to yellow, generally present, +1–2 mm +long; appendages absent or present, green, horizontally spreading, ovate-triangular, 1–4 by +2.5–3.5 cm +; bracteole boat-shaped, +23–25 mm +long, callus whitish, +2–4 mm +long; calyx pale green to white, +12–20 mm +long, lobes broadly ovate-triangular, +3–5 mm +long, callus absent or present and then < +1 mm +long; co- rolla hyaline, reddish brown to purplish grey to white, +40–50 mm +long, glabrous, tube +15–20 mm +long, lobes with dark red margins, narrowly ovate, +30–35 mm +long; labellum at the outer basal part whitish, outer upper part reddish brown to purplish grey, inner side white with yellow to white central nectar guide and brown purplish-striped lateral parts, funnel-shaped, broadly obovate when spread out, 35–40 by +35–40 mm +, margin crenu- late; stamen white, c. 30 by +10 mm +, apex white with narrow pink margin, anther +8 –10 mm +long. +Capsule +and +seeds +not seen. + + + + + + + + + + + +
+(( + +( +
(
+
+ + +Map 12 +Distribution of + +Costus maboumiensis +Pellegr. + +(■) and + +C. nimba +H.Maas & Maas + +(●). + + + + +Map 11 +Distribution of + +Costus lucanusianus +J.Braun & K.Schum. + + + + +Distribution — Central Africa (Gabon). + + + +Habitat & Ecology — In primary or secondary rainforest. At elevations of + +0– +530 m. + +Flowering and fruiting: October and November. + + + + +IUCN Conservation Status — + +Costus maboumiensis + +has an AOO of +36 km +2 +and occurs in five locations (we consider the southern and northern Doudou Mountains as two locations) of which only one partly has a protected status, while the others are in areas with more or less logging pressure. We assess the species as Endangered ( +EN +) B2ab(ii,iii). + + + + +Notes — + +Costus maboumiensis + +is recognizable by a combi- nation of the following characters: inflorescence terminating a separate shoot covered with reddish brown sheaths and reddish brown flowers, a colour never seen in any other African species. Furthermore all parts of the plant lack indument. + +Costus maboumiensis + +shares with + +C. dubius + +a basal inflorescence, but strongly differs by the colour of the flowers, which are dark reddish brown in + +C. maboumiensis + +and white in + +C. dubius +. + + + +
+
\ No newline at end of file diff --git a/data/38/76/87/387687E2BB26FFECFC84FE3FFE0BFEA4.xml b/data/38/76/87/387687E2BB26FFECFC84FE3FFE0BFEA4.xml new file mode 100644 index 00000000000..9af21e2aa21 --- /dev/null +++ b/data/38/76/87/387687E2BB26FFECFC84FE3FFE0BFEA4.xml @@ -0,0 +1,275 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +15. + +Costus loangensis +H.Maas & Maas + + +— +Map 7 + + + + + + +Costus loangensis +H.Maas & Maas (2012) + +12, f. 1. — +Type +: +Maas et al. 10184 +(holo +WAG +2 +sheets [ +WAG0380168 +, +WAG0380169 +]; + + +iso +K +, +LBV +, +MO +, +P +, +UC +), +Gabon +, +Ogooué-Maritime +, +Parc Nacional de Loango +, +between Lodge and Staff building +, +wet forest on white sand +, +along forest trail +, +at about sea level +, + +9 Nov. 2011 + + +. + + + + + +Etymology. +Costus loangensis + +is named after the place where it has been collected near Loango Lodge, in Parc Nacional de Loango in Gabon. + +Costus loangensis + +was discovered upon seeing a photograph of an unknown + +Costus + +in Vande Weghe’s book on plants and animals of Gabon’s National Parks (2007:278, f. 623).He describes and publishes a photo of a specimen of + +Costus + +‘which seems to be quite typical for these coastal forests’. We, however, found only a single population. + + + + +Terrestrial herb, +0.5–0.6 m +tall, shoots dark brownish red. +Leaves +few (6–7) concentrated at the apex of the shoot; sheaths dark red, +0.6–0.8 cm +diam; ligule membranous, 2-lobed, +15–18 mm +long; petiole +5–6 mm +long; sheaths sparsely to rather densely covered with erect to half-appressed hairs c. +2 mm +long, ligule and petiole densely to rather densely so; lamina dark olive-green, zone along midrib sometimes reddish, nar- rowly elliptic to elliptic, 14–16 by +5–6 cm +, densely to rather densely covered with erect to half-appressed hairs +1.5–2 mm +long on both sides, base attenuate, apex acute. +Inflorescence +3–5-flowered, ovoid, c. 2 by +1–1.5 cm +, terminating the leafy shoot; outer side of bracts, bracteoles and calyx densely covered with appressed to half-appressed hairs < +1 mm +long, ovary sparsely so. +Flowers +1 per bract; bracts reduced, brown to reddish brown, chartaceous, narrowly ovate-triangular to ovate-triangular, 1.7–2 by +0.5–1 cm +, callus +2.5–3 mm +long; appendages absent; bracteole boat-shaped, +15–18 mm +long, callus +1.5–2 mm +long; calyx +11–12 mm +long, lobes deltate, c. +2 mm +long, callus c. +1 mm +long; corolla yellow, +50–55 mm +long, rather densely covered with half-appressed hairs < +1 mm +long, particularly near the apex, tube +20–25 mm +long, lobes narrowly elliptic, +30–35 mm +long, together forming a hood over the throat opposite the labellum, apex with a callus-like thickening; labellum completely yellow, horizontally flattened with funnel-shaped base, broadly obovate when spread out, 30–40 by +40–50 mm +, margin fimbriate (fimbriae +2–3 mm +long); stamen yellow, 25–30 by +7–10 mm +, anther +5–7 mm +long. +Capsule +and +seeds +not seen. + + + + +Distribution — Central Africa ( +Gabon +). Only known from the +type +collection. + + + +Habitat & Ecology — In wet rainforest, on white sand, at elevations of about sea level. Flowering and fruiting: November. + + + +IUCN Conservation Status — + +Costus loangensis + +has only been collected once ( +AOO += +4 km +2 +), just outside a National Park. Although this locality is within the buffer zone around the park, this locality is used for the construction of tourist accommodations. To our knowledge there exist only few mature individuals of this species. We therefore access this species as Critically Endangered ( +CR +) B2ab(iii,v); +D +. + + + + +Notes — + +Costus loangensis +, + +known only from the +type +collection, is a species of small (c. +0.5 m +tall) plants with few (6 or 7) leaves, completely yellow flowers and unappendaged bracts. Shoots and leaves are covered with a dense indument of erect to half-appressed hairs. + +Costus loangensis + +differs from the very similar + +C. ligularis + +, another species of small size with a dense indument, by the colour of its flowers; those of + +C. ligularis + +are pale pink rather than bright yellow in + +C. loangensis + +. Moreover, the bracts of + +C. ligularis + +are generally appendaged. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB27FFECFFCDFE9FFB03FAA9.xml b/data/38/76/87/387687E2BB27FFECFFCDFE9FFB03FAA9.xml new file mode 100644 index 00000000000..8f3222593b1 --- /dev/null +++ b/data/38/76/87/387687E2BB27FFECFFCDFE9FFB03FAA9.xml @@ -0,0 +1,277 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +16. + +Costus louisii +H.Maas & Maas + + +, + +sp. nov. + +— +Plate 4f +; +Map 10 + + + + + +Costus louisii + +looks superficially like + +C. afer + +but can be distinguished by having shiny leaves, 1 flower per bract, shiny green bracts and completely pinkish red flowers. — + + + + + +Type +: +Maas et al. 10339 +(holo +WAG +; + + +iso +K +, L-spirit [ +L0298233 +], +LBV +, +MO +, +UC +), +Gabon +, +Estuaire +, +Libreville +, +Glass +, garden of +A.M. Louis +, at sea level, + +6 Nov. 2011 + +, cultivated from a +specimen +collected by +A.M. Louis +, + +30 km +S of Mayumba + +, within walking distance of the ocean, on white sand, in swampy low forest + +. + + + + +Terrestrial herb +1.5–2.5 m +tall. +Leaves +many; sheaths +0.8–1.1 cm +diam; ligule chartaceous, unequally 2-lobed, +10–29 mm +long, apical margin with white curly fibers; petiole +5–10 mm +long; sheaths, ligule and petiole glabrous except for some long hairs at the very base of the leaves, many on the upper margin of the ligule and also some on the border between the petiole and the sheath; lamina upper side dark green, lower side pale green, shiny at both sides or only at the upper side, narrowly ovate-elliptic (to obovate), 20–29 by +6–10 cm +, both sides and margin glabrous except for some erect hairs < +1 mm +long, base acute (to slightly cordate), apex acuminate (acumen +15–35 mm +long). +Inflorescence +many-flowered, ovoid, (4–)7–10 by +4–6 cm +, terminating the leafy shoot; bracts, appendages of bracts, bracteoles, calyx and ovary glabrous. +Flowers +1(–2) per bract; bracts basally green with shiny brown to dark red upper part, coriaceous, broadly ovate-triangular to ovate-triangular, 2–3 by +2–3 cm +, callus absent; appendages generally absent; bracteole boat-shaped, +20–21 mm +long, callus (pale) green c. +2 mm +long; calyx +17–21 mm +long, lobes triangular, +3–4 mm +long, callus absent; corolla white, +50–60 mm +long, glabrous, tube +10–15 mm +long, lobes white with pink apex and yellow base, narrowly elliptic, +40–45 mm +long; labellum at the outer side white, inner side basally white, upper part completely (striped with) dark pink, throat and nectar guide yellow, horizontally flattened, broadly obovate to circular when spread out, 45–50 by +50–55 mm +, margin crenate and undulate; stamen white with dark pink apex, 30–35 by +10–15 mm +, apex (dark) pink, anther +7–8 mm +long. +Capsule +and +seeds +not seen. + + + +Distribution — Central Africa (Gabon). + + +Habitat & Ecology — In swampy low forest or savanna, on white sand, at elevations of about sea level. Flowering and fruiting: November. + + +Field observations — The plants are pollinated by small birds; capsule and seeds were never seen (A.M. Louis, pers. comm.). + + + +IUCN Conservation Status — This species is only known from a single wild collection ( +AOO += +4 km +2 +) from a small popula- tion, and one plant in cultivation. This location does not have any protected status.Although it is not immediately threatened, there is some tourism development in the area. We assess this species as Critically Endangered ( +CR +) B2ab(iii,v); +D +. + + + + +Notes — + +Costus louisii + +looks very much like + +C. afer + +, both having many-flowered inflorescences that terminate the leafy shoots. In + +C. louisii + +, however, the leaves are shiny at both sides, whereas the leaves of + +C. afer + +are never shiny. Moreover, the labellum of the flowers of + +C. louisii + +is horizontally flattened and completely dark pink with yellow nectar guide, while that of + +C. afer + +is funnel-shaped and white with a yellow nectar guide and red colouring restricted to the margins. The material of + +C. louisii + +has all been collected from plants now in cultivation in the greenhouses of Burgers’ Bush,Arnhem, +The Netherlands +and of Royal Botanic Gardens, Kew, London, + +Great Britain +. + + +They originate from the +type +specimen +growing in the garden of +A.M. Louis +, who collected it + +30 km +S of Mayumba + +, +Gabon +, within walking distance of the ocean, on white sand, in +swampy low forest +( +S3°36’ +E10°52’ +) + +. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB27FFEEFC84FA91FB78FD43.xml b/data/38/76/87/387687E2BB27FFEEFC84FA91FB78FD43.xml new file mode 100644 index 00000000000..20d6e9b7637 --- /dev/null +++ b/data/38/76/87/387687E2BB27FFEEFC84FA91FB78FD43.xml @@ -0,0 +1,427 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +6c0dbc52-820c-4f68-912d-1bcaa2227efc +7570023 + + + + + +17. + +Costus lucanusianus +J.Braun & K.Schum. + + +— +Fig. 4d +; +Map 11 + + + + + + +Costus lucanusianus +J.Braun & K.Schum.(1889) + +151; K.Schum.(1904) 392. — Type: +Braun s.n. +(holo +B +destroyed), +Cameroon +, +South Province +, +Batanga.As +the +holotype +was destroyed in +Berlin +and no other type material has been located + + +we hereby select a +neotype +from a locality not far from the type locality: + + +Van Andel + +et al. 3406 + +(neo +WAG +[ +WAG0145874 +] + +; + +isoneo +KRIBI +), +Cameroon +, +South Province +, +Campo-Ma’an National Park +, +Ntem River +, +Ebianemeyong +, +at the foot of Asuangale falls +, + +350 m + +, + +6 May 2001 + + +. + + + + + + +Costus lucanusianus +J.Braun & K.Schum. var. +major +K.Schum. (1904) + +392, syn. nov. — +Syntypes +: +Braun s.n. +( +B +destroyed), +Cameroon +, +South Province +, Gross-Batanga + +; + +Zenker 1595 +( +BM +, +E +, +G +, +K +, +L +, +LE +, +M +, +MO +, +P +, +S +, +WRSL +) + +, + +Cameroon +, +South Province +, Bipindi, +14 Dec. 1894 + +. + + + + +Costus dussii +K.Schum. (1904) + +402,f. 45B; Maas (1972) 121. — +Type +: +Duss 2109b +(holo +B +destroyed; lecto +NY +, selected by Maas 1972), +Martinique +, ‘Hauteurs du Carbet et Fonds Saint Denis’ + +. + + + + +Terrestrial herb, erect but in fruit often bending down, +1–5 m +tall. +Leaves +many; sheaths +0.5–2 cm +diam; ligule truncate to slightly 2-lobed, 1–4(–8) mm long, with a basal horizontal rim +1–2 mm +high provided with a prominent row of needle-like hairs +2–6 mm +long; petiole +4–10 mm +long; sheaths, ligule and petiole rather densely to sparsely covered with erect hairs < +1 mm +long to glabrous; lamina narrowly elliptic, 12–33 by +3–10 cm +, up- per side glabrous, lower side densely to sparsely covered with silvery, mainly erect hairs to c. +2 mm +long to glabrous, base obtuse to cordate, apex acuminate (acumen +10–20 mm +long), margin undulate. +Inflorescence +many-flowered, broadly ovoid to globose, 2–12 by +2–9 cm +, sometimes elongating to c. +20 cm +in fruit, terminating the leafy shoot; bracts, bracteoles, calyx, ovary and capsule glabrous or sparsely covered with erect and appressed hairs < +1 mm +long, calyx lobes often rather densely hairy, particularly along the margins. +Flowers +2 per bract; bracts green, coriaceous, broadly to very broadly ovate-triangular, 1.5–3 by +1.5–3 cm +, falling apart into separate fibers with age, callus inconspicuous, up to c. +2 mm +long; appendages absent; bracteole boat-shaped, +17–20 mm +long, callus +2–4 mm +long; calyx +18–25 mm +long, lobes broadly ovate-triangular to trian- gular, +4–12 mm +long, horizontally spreading to reflexed, in fruit distinctly exceeding the bracts, callus sometimes present and then +2–3 mm +long; corolla white, +30–45 mm +long, glabrous, tube +10–15 mm +long, lobes elliptic, +25–30 mm +long; labellum at the outer side white with dark red upper part, inner side basally white with wide dark reddish margin and yellow to orange nectar guide, funnel-shaped, broadly obovate when spread out, 40–50 by +40–45 mm +, margin crenate; stamen white, 30–35 by +10–15 mm +, apex dark pink, anther +6–11 mm +long. +Capsule +ellipsoid to broadly ellipsoid, 10–20 by +5–15 mm +. +Seeds +1–2 by +1–1.5 mm +. + + + + +Map 10 +Distribution of + +Costus louisii +H.Maar & Maas + +(▲) and +C. tappen- beckianus +(●). + + + + +Plate 4 +a. + +Costus macranthus +K.Schum. Habit + +, flower and details of stamen, stigma and style. – b. + +Costus nimba +H.Maas & Maas. + +Basal inflorescence. – c. + +Costus spectabilis +(Fenzl) K.Schum.Habit + +with flowers. – d. + +Costus lucanusianus +J.Braun & K.Schum. Inflorescence + +with 4 flowers.– e. + +Costus talbottii +Ridl. Flower. + +– f. + +Costus louisii +H.Maas & Maas. Inflorescence + +(a: Wright 1905: t 7992; b: +Jongkind 11301 +; c: photographed in Rumonge, SW Burundi, no specimen collected; d: +Maas et al. 10000 +; e: +Maas et al. 9800 +; f: +Maas et al. 10339 +). — Photos: a, b, d–f: P.J.M.Maas; c: E. Fischer. + + + +Distribution — North East Africa (Ethiopia, South Sudan); West Africa (Benin, Ghana, Guinea, Ivory Coast, Liberia, Ni- geria, Sierra Leone, Togo); Central Africa (Burundi, Cameroon, Central African Republic, Congo Brazzaville, Congo Kinshasa, Equatorial Guinea, Gabon, São Tomé & Principe); East Africa (Uganda); Southern Tropical Africa (Angola). + + + +Habitat & Ecology — In savanna forest, secondary forest and swamp forest, in wet places along rivers and road sides, and in plantations, at elevations of +0–1700 m +. Flowering and fruiting: all year through. + + + +Field observations — Often plants are viviparous, the seedlings emerging from the ripe fruit. As the shoot with the heavy infructescence bends down and reaches the ground, the plantlets can start their life easily. + + +IUCN Conservation Status — Least Concern. + + + +Notes — + +Costus lucanusianus + +can easily be recognized by having a row of distinct erect hairs on a horizontal rim at the base of a very short ligule. The flowers have horizontally spreading to reflexed calyx lobes. The labellum is completely white at the outer side contrasting with the inner side which has a dark red margin and dark yellow nectar guide. The lower side of the leaves is densely to sparsely covered with silvery hairs to glabrous. The apex of the stamen is pink and narrowly triangular. Boat-shaped bracteoles can be so compressed inside the inflorescence that they become 2-keeled. + +Costus lucanusianus + +is sometimes confused with + +C. afer + +. + +Costus lucanusianus + +is characterized, however, by a complete ring of hairs on the nodes, while in + +C. afer + +this ring is incomplete and less hairy. The lower side of the leaves is generally hairy in + +C. lucanusianus + +and glabrous in + +C. afer + +. The calyx lobes of + +C. lucanusianus + +are horizontally spreading to reflexed and those of + +C. afer + +are erect. The ligule in + +C. lucanusianus + +is +1–4 mm +long vs +4–11 mm +in + +C. afer +. + +The bracts of + +C. lucanusianus + +are green, those of + +C. afer + +are reddish. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB29FFE2FFCDFE9FFA16FE53.xml b/data/38/76/87/387687E2BB29FFE2FFCDFE9FFA16FE53.xml new file mode 100644 index 00000000000..1a4b55f1738 --- /dev/null +++ b/data/38/76/87/387687E2BB29FFE2FFCDFE9FFA16FE53.xml @@ -0,0 +1,316 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +13. + +Costus ligularis +Baker + + +— +Fig. 1f +; +Map 4 + + + + + + +Costus ligularis +Baker (1898) + +298; K.Schum. (1904) 390. — +Type +: +Mann 1628 +(holo +K +2 +sheets), +Equatorial Guinea +, +Litoral Prov +., +Corisco Bay +, +Muni River +(‘ +Danger River’ +), + +Aug. 1862 + + +. + + + + +Costus araneosus +Gagnep. (1902a) + +95, syn. nov. — +Type +: +De Brazza 100 +(holo +P +), +Congo Brazzaville +, +Brazzaville +, + +Sept.-Oct. 1884 + + +. + + + + +Costus fimbriatus +Pellegr. (1929) + +220, syn. nov. — +Type +: +Le Testu 1817 +(holo +P +; + + +iso +BM +, +BR +, +P +), +Gabon +, +Nyanga +, +Tchibanga area +, +Maboumi Camp +, +Mayombe bavili +, + +27 Oct. 1914 + + +. + + + + +Costus ngouniensis +Pellegr. (1938) + +41, nom.nud., without Latin description. — Based on: +Le Testu 2238 +( +BM +, +BR +, +P +), +Gabon +, +Ngounié +, +Nzouna +, + +22 Oct. 1917 + + +. + + + + +Terrestrial herb 0.3–0.5(–1.5) m tall. +Leaves +2–6(–8), often condensed at the top of the shoot in an apical rosette; sheaths dark red, +0.2–1.5 cm +diam, sometimes creamy, falling apart into separate fibers with age; ligule dark reddish brown, mem- branous, truncate or 2-lobed, +5–50 mm +long; petiole +3–15 mm +long; sheaths, ligule and petiole densely to sparsely covered with erect hairs to c. +3 mm +long; lamina sometimes red to purple on lower side, narrowly obovate to elliptic, 9–23 by +4–10.5 cm +, 3–5-plicate ( +Maas et al. 10212 +), chartaceous, upper and lower side densely to sparsely covered with soft erect hairs to c. +3 mm +long, base acute, apex acute to acuminate (acumen 10(–15) mm long). +Inflorescence +few- to several-flowered, broadly ovoid to globose, 1–4 by +1–4 cm +, terminating the leafy shoot or rarely terminating a separate leafless shoot 2–7(–20) cm long; bracts, appendages of bracts, bracteoles, calyx and ovary sparsely to rather densely covered with appressed hairs < +1 mm +long. +Flowers +1 per bract; bracts apically dark brown-red with darker dots, chartaceous, ovate to broadly ovate, 0.8–1.8 by +0.5–2.4 cm +, callus absent or present and +1–2 mm +long; appendages generally present, brownish red, ascending, horizontally spreading or reflexed, broadly ovate, 0.2–0.7(–2) by 0.2–0.5(–2) cm, bracteole boat-shaped, +7–15 mm +long, callus distinct, yellowish to whitish, +1.5–2 mm +long; calyx whitish with pink upper part, +5–12 mm +long, lobes shallowly triangular, +1–2 mm +long, callus absent; corolla hyaline, pink to red to brown, +55–65 mm +long, glabrous, tube +10–15 mm +long, lobes narrowly elliptic, +45–55 mm +long; labellum white to pink on the outer side, inner side white with broad pink to purple margin, base of throat often yellow, no nectar guide present, horizontally flattened, broadly obovate when spread out, 50–80 by +40–70 mm +, margin fimbriate, more or less 5-lobed, and crenate; sta- men white, 30–40 by +10–20 mm +, apex yellow to orange, very tip pink, anther +5–8 mm +long. +Capsule +and +seeds +not seen. + + + +Distribution — Central Africa (Cameroon, Congo Brazzaville, Equatorial Guinea, Gabon). + + + +Habitat & Ecology — In rainforest, sometimes growing along river banks, in lateritic to sandy soils, at elevations of + +0– +800 m. + +Flowering and fruiting: all year through, especially in January. + + + +IUCN Conservation Status — Least Concern. + + + +Notes — + +Costus ligularis + +is a species of small stature that can be distinguished by its dark red sheaths, softly hairy leaves (on both sides), small and dark reddish brown appendaged bracts, very distinct calli on the bracteoles, a pinkish labellum without nectar guide and a relatively small inflorescence (1–4 by +1–4 cm +). The absence of a nectar guide inside the throat of the + +C. ligularis + +flower is functionally ‘replaced’ by the yellow apex of the stamen, which is turned upwards and highly visible. + +Costus ligulari + +s differs from the similarly looking + +C. phyllocephalus + +by having a small inflorescence of 1–4 by +1–4 cm +, com-posed of relatively small dark reddish brown bracts, bracteoles and calyx. The bracts are +0.8–1.8 cm +long, the appendages +0.2–0.7 cm +long. The bracteoles are +7–15 mm +long with a callus of +1.5–2 mm +long. This yellowish callus is prominently visible contrasting with the dark reddish brown bracteole. In contrast + +C. phyllocephalus + +has an inflorescence of 2.5–10 by +3–7 cm +, composed of relative large, green to reddish purple bracts, bracteoles and calyx. The bracts are +1–2.5 cm +long, the appendages +1–4.5 cm +long. The bracteoles are +11–21 mm +long with a callus +2–3.5 mm +long; this callus is not very distinct. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB29FFEDFC84FE0CFA16FE02.xml b/data/38/76/87/387687E2BB29FFEDFC84FE0CFA16FE02.xml new file mode 100644 index 00000000000..1acc588def6 --- /dev/null +++ b/data/38/76/87/387687E2BB29FFEDFC84FE0CFA16FE02.xml @@ -0,0 +1,596 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +14. + +Costus lilaceus +Maas & H.Maas + + +, + +sp. nov. + +— +Plate 3d +; +Map 9 + + + + + +Costus lilaceus + +can be recognized by its often epiphytic habit, pink to lilac flowers and its inflorescences placed laterally in the axil of a leaf or termi- nating a separate leafless shoot. — + + + + + +Type +: +J.J.F.E. de Wilde et al. +( +WALK-B series +) +40 +(holo +WAG +2 +sheets [ +WAG0114490 +, +WAG0114491 +]; + + +iso +BR +, +C +, +LBV +, +MO +, +P +), +Gabon +, +Woleu-Ntem +, +Crystal Mountains +, + +7 km +along the road from Tchimbélé to Kinguélé + +, + +620 m + +, + +18 Jan. 1983 + + +. + + + + +Epiphytic or sometimes terrestrial herb +0.3–1.6 m +tall. +Leaves +many; sheaths +0.3–0.8 cm +diam; ligule reddish brown to orange, membranous, truncate, 20–60(–80) mm long, often longer than the internode; petiole +2–15 mm +long; sheaths, ligule and petiole glabrous; lamina shiny bright or pale green at upper side, less shiny, sometimes purplish or glaucous at lower side, (narrowly) elliptic or rarely (ob)ovate, more or less falciform, 9–30 by +3–8 cm +, coriaceous and somewhat fleshy, glabrous on both sides, base acute to obtuse, apex acute to acuminate (acumen +15–20 mm +long). +Inflorescences +generally several per flowering branch, each one few- to several-flowered, ovoid to ellipsoid, (1–)1.5–5 by +1–2.5 cm +, lateral in the axil of a leaf with a peduncle +0.5–2.5 cm +long or terminating a separate leafless shoot emerging from the rhizome +0.8–1 cm +long or terminating a leafy shoot; bracts, bracteoles, calyx, ovary and capsule sparsely to rather densely covered with erect hairs < +1 mm +long. +Flowers +1 per bract; bracts dark reddish brown to dark green with red dots, old bracts (pale) brown, chartaceous, narrowly to broadly elliptic-(ob)ovate, 0.3–1.1 by +0.1–1.1 cm +, callus yellowish green, +0.5–1.5 mm +long, sometimes inconspicuous; appendages absent; bracteole tubular, +7–9 mm +long, callus green, +1–1.5 mm +long; calyx pale green to crimson to dark reddish brown, +7–23 mm +long, lobes shallowly triangular +1–2.5 mm +long, callus yellowish green, +1–2 mm +long; corolla hyaline, white, +30–50 mm +long, glabrous, tube +10–15 mm +long, lobes narrowly elliptic, +30–40 mm +long; labellum at the outer side basally white, upper part pale lilac, inner side pale pink to lilac or rarely white (see note), with bright yellow to orange nectar guide and reddish dots and hairs at the base, horizontally flat- tened with funnel-shaped base, broadly obovate when spread out, 35–70 by +30–65 mm +, margin irregularly crenate undulate; stamen white to pale pink with reddish dots, 30–35 by +10–12 mm +, apex bright yellow, anther +9–10 mm +long. +Capsule +ellipsoid to broadly ellipsoid, 6–7 by +4 mm +. +Seeds +c. +1 mm +diam. + + + + +Map 9 +Distribution of + +Costus lilaceus +Maas & H.Maas + +(●) and + +C. talbotii +Ridl. + +(▲). + + + +Distribution — West Africa (Nigeria); Central Africa (Cam- eroon, Congo Brazzaville, Congo Kinshasa, Equatorial Guinea, Gabon). + + + +Habitat & Ecology — In primary or sometimes secondary rainforest, in wet places (epiphytic specimens), but also in savanna forest in rocky places or on outcrops (terrestrial speci- mens), at elevations of +80–1530 m +. Flowering and fruiting: all year through, especially in January. + + + + +IUCN Conservation Status — This species with about 22 locations and an AOO of +248 km +2 +is assessed as Least Concern ( +LC +). + + + + + +Representative specimens examined +. +CAMEROON +, + +Littoral Province + +, +Forêt de Bakaka +, +3 km +E of Eboné (on km 11 of Nkongsamba-Loum Road), +520 m +, +28 Jan. 1972 +, +Leeuwenberg 9317 +( +BR +, +K +, +MO +, +P +, +WAG +, +YA +) + +. + + +South Province + +, Lolodorf, +8 Jan. 1968 +, +Bamps 1748 +( +BR +) + +. + + +South-West Province + +, Mts Rumpi, near Dikome Balue, +35 km +NNW of Kumba, +1200 m +, +25 Mar. 1976 +, +Letouzey 14578 +( +P +), + + +Bakossi Mts, W of Bangem, +1400 m +, +3 Jan.1986 +, +D.W. Thomas 5262 +( +MO +, +NY +) + +. – + +CONGO BRAZZAVILLE +, +Kouilou +, cultivated at Pointe Noire, originating from Maiombe, région de Dimonika, +29 Oct. 1988 +, +De Foresta 1739 +( +P +) + +. + +Niari +, border of +Congo Brazzaville +and Gabon, +500 m +from the Loambitsi River, +4 Feb. 1975 +, + +Sita +3884 + +( +BR +) + +. – + +CONGO KINSHASHA +, +Nord-Kivu +, Kitshanga, +1300 m +, +7 Jan. 1959 +, +A +. +Léonard 2348 +( +BR +) + +. + +Sud- Kivu +, Territoire Kalehe,km 110 of road from Kavumu to Walikale,Irangi,near River Luhoho, +850 m +, +6 Dec. 1956 +, +Christiaensen 1920 +( +BR +, +U +) + +. – + +EQUATORIAL GUINEA +, + +Centro Sur + +, Bata-Monte Alén, +18 Mar. 1994 +, +Carvalho 5488 +( +WAG +) + +; + +Parque Nacional de Monte Alén, near Lago Atok, +2 July 1998 +, +Pérez Viso 19 +( +WAG +) + +. – + +GABON +, +Estuaire +, Monts de Cristal, Mkam-Mela, +950 m +, +30 Jan. 1968 +, +Hallé & Villiers 4746 +( +P +) + +. + + +Ngounié + +, +25 km +NE of Mouila, +19 Dec.1985 +, +Wilks 1166 +( +WAG +) + +. + + +Nyanga + +, +25 km +SW of Doussala, +11 Jan. 1987 +, +Reitsma & Reitsma 2835 +( +MO +, +NY +, +WAG +) + +. + +Ogooué-Ivindo +, road on Babiel-Nord, few kms W of Belinga, +900 m +, +18 July 1985 +, + +Bos +et al. 10685 + +( +BR +, +MO +, +WAG +) + +. – + +NIGERIA +, +Ogoja +, Ikwette-Balegeta path, +4500 ft +, +29 Dec. 1948 +, + +Savory & Keay +FHI +25202 + +( +K +, +P +) + +. + + + + +Notes — + +Costus lilaceus + +can only be separated from + +C. lateriflorus + +by the colour of the labellum of the flowers being yellow in + +C. lateriflorus + +but pink to lilac in + +C. lilaceus + +. Many specimens have wrongly been identified as + +C. letestui + +, assuming the flowers of this species were lilac in colour (Koechlin 1964, 1965). As + +C. letestui + +turned out to be a synonym of + +C. lateriflorus + +(see under that species), these specimens with pink to lilac flowers needed a new name: + +C. lilaceus + +. + +Costus lilaceus + +has been found epiphytic in trees up to +25 m +high on + +Parkia bicolor +( +Bamps 1612 +) + +, + +Gilbertiodendron dewevrei + +( +Christiaensen 1826 +and +1920 +) and + +Julbernardia + +( +Letouzey 12730 +). The plant forms a clump with pendant shoots. When terrestrial it is often found at high altitude growing over rock, forming a ‘dense mat of + +Costus + +between the trees and shrubs’ ( +A.M. Louis 2318 +). Studying the distribution of + +C. lilaceus + +and + +C. lateriflorus + +we found a difference in the altitude where both species occur: + +C. lilaceus + +is generally found growing at higher elevations ( +80–1530 m +), avoiding the sedimentary basin; + +C. lateriflorus + +seems to prefer the coastal sedimentary areas of +Gabon +and +Cameroon +( +0–800 m +). Some specimens of + +C. lilaceus + +have flowers with a very pale lilac to almost white labellum and a bright yellow nectar guide. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB2AFFE1FFCDFBC7FC57FDD2.xml b/data/38/76/87/387687E2BB2AFFE1FFCDFBC7FC57FDD2.xml new file mode 100644 index 00000000000..5539d35c10a --- /dev/null +++ b/data/38/76/87/387687E2BB2AFFE1FFCDFBC7FC57FDD2.xml @@ -0,0 +1,296 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +6c0dbc52-820c-4f68-912d-1bcaa2227efc +7570023 + + + + + +11. + +Costus kupensis +Maas & H.Maas + + +, + +sp. nov. + +— +Fig. 5 +; +Plate 3a +; Map 6 + + + + + +Costus kupensis + +can easily be recognized by its yellow flowers and an inflo- rescence terminating a separate leafless shoot, a combination of characters not seen in any other African species of + +Costus + +. — + + + + + +Type +: +Cheek et al. 7111 +(holo +K +; + + +iso +L +, +SCA +, +WAG +, +YA +), +Cameroon +, +South-West Province +, hunters path from +Kupe Village +to mountain top, + +840 m + +, + +24 Jan. 1995 + + +. + + + + + +Costus sp. A +. + +Cheek in Cheek et al. (2004) 434, pl. 15E. + + + + +Terrestrial herb +1.5–3 m +tall. +Leaves +many; sheaths +1–2.5 cm +diam, dark red; ligule chartaceous, 2-lobed, +5–18 mm +long; petiole +5–10 mm +long; sheaths, ligule and petiole rather densely covered with appressed to erect hairs < +1 mm +long; lamina narrowly obovate-elliptic, 20–27 by +6–9 cm +, upper side glabrous, lower side sparsely to rather densely covered with erect hairs < +1 mm +long on margin and midrib to glabrous, base acute, apex acuminate (acumen +15–20 mm +long). +Inflorescence +many-flowered, ovoid, 4–9 by +3–4 cm +, terminating a separate leafless shoot +3–15 cm +long; (upper part of) bracts and capsule sparsely to rather densely covered with appressed to erect hairs < +1 mm +long, bracteole with a row of erect hairs on the keel, calyx glabrous. +Flowers +1 per bract; bracts dark reddish brown, coriaceous, broadly to depressed ovate, 1–2 by +1.5–2.5 cm +, callus sometimes present and then c. +2 mm +long; appendages absent; bracteole boat-shaped, +18–22 mm +long, callus c. +1 mm +long; calyx +12–16 mm +long, in fruit exceeding the bracts, lobes narrowly to broadly triangular, +2–5 mm +long, callus absent; corolla yellow, upper part of lobes pinkish, +55–60 mm +long, glabrous, tube c. +15 mm +long, lobes narrowly elliptic, +40–45 mm +long; labellum yellow, with dark yellow nectar guide, funnel-shaped to horizontally flattened, broadly obovate when spread out, c. 50 by +50 mm +; stamen yellow, c. 40 by +14 mm +, apex recurved, anther +7–8 mm +long. +Capsule +ellipsoid, c. 11 by +6 mm +. +Seeds +c. 2 by +1.5 mm +. + + + +Distribution — Central Africa (Cameroon). + + + +Habitat & Ecology — In rainforest. At elevations of +800– 1000 m +. Flowering and fruiting: January, May and October. + + + + +IUCN Conservation Status — Based on an EOO of +1419 km +2 +and an AOO of +12 km +2 +, occurring on 3 locations, none of which currently has a protected status and one might be already lost, we assess this species as Endangered ( +EN +) B1ab(i,ii,iii,iv,v)+ 2ab( +I +,ii,iii,iv,v). + + + + + +Other specimens examined. +CAMEROON +, + +Littoral Province + +, Ebo proposed National Park, Yingui, CRES camp on trail to Iboti, +800 m +, +23 Apr. 2005 +, +Cheek et al. 12498 +( +K +, +YA +); + + +Mont Nlonako, +5 km +SSE of Nkongsamba, +1000 m +, +17 Mar.1976 +, +Letouzey 14456 +( +K +, +P +). + + + +South-West Province + +, Kupe- Muanenguba Division, Kupe Village, vicinity of saprophyte site on Daniel Ajang’s bush, +870 m +, +20 May1996 +, +Cable et al. 2471 +( +K +, +U +, +WAG +, +YA +) + +. + + + + +Note — The description is partly based on our observations on a living plant in Burgers’ Bush, vouchered as +Maas & Maas 10575 +. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB2AFFE2FC84FD8DFD28FEA4.xml b/data/38/76/87/387687E2BB2AFFE2FC84FD8DFD28FEA4.xml new file mode 100644 index 00000000000..c73fdfc1c77 --- /dev/null +++ b/data/38/76/87/387687E2BB2AFFE2FC84FD8DFD28FEA4.xml @@ -0,0 +1,349 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +12. + +Costus lateriflorus +Baker + + +— +Plate 3b +; +Map 8 + + + + + + +Costus lateriflorus +Baker (1898) + +301; K.Schum. (1904) 413. — +Type +: +Mann 1629 +(holo +K +; + + +iso +P +), +Equatorial Guinea +, +Litoral Prov +., +Corisco Bay +, +Mount John +, +River Kongui +, + +Aug. 1862 + + +. + + + + + + +Costus letestui +Pellegr. (1929) + +220 (as ‘ +Le Testui +’), syn. nov. — +Type +: +Le Testu 1683 +(holo +P +; + + +iso +BM +, +K +), +Gabon +, +Nyanga +, +Tchibanga +area, +Mayombe bayaka +, +Ighouma +, + +8 km +NE from Mouila + +, + +12 Jan. 1913 + + +. + + + + +Epiphytic or sometimes terrestrial herb to c. +1.5 m +tall. +Leaves +many; sheaths +0.4–0.7 cm +diam; ligule reddish brown, mem- branous, truncate, +25–40 mm +long, sometimes longer than the internode; petiole +4–10 mm +long; sheaths, ligule and petiole glabrous; lamina sometimes purplish on lower side, coriaceous and somewhat fleshy, narrowly elliptic, 9–20 by +2–6.5 cm +, glabrous on both sides, base acute to obtuse, apex acuminate (acumen +5–12 mm +long). +Inflorescences +generally several per flowering branch, each one few- to several-flowered, ovoid, 2–4 by +1–3 cm +, lateral in the axil of a leaf with a peduncle +1–4 cm +long or terminating a separate leafless shoot c. +1 cm +long or terminal on a leafy shoot; bracts, bracteoles, calyx, ovary and capsule rather densely to densely covered with erect hairs < +1 mm +long, rarely glabrous. +Flowers +1 per bract; bracts pale brownish green to reddish brown, slightly dotted with pink, chartaceous, ovate, 0.5–1 by +0.3–0.8 cm +, callus sometimes present and then c. +1 mm +long; appendages absent; bracteole tubular, +8–12 mm +long, callus sometimes present and then c. +1 mm +long; calyx pale pinkish green to reddish brown with pale green lobes, +12–18 mm +long, lobes shallowly ovatetriangular, +1–2 mm +long, callus distinct, green, +1–2 mm +long; corolla hyaline, whitish with some pink or brown and red dots, +35–50 mm +long, glabrous, tube +15–20 mm +long, lobes narrowly elliptic-ovate, +20–35 mm +long; labellum at the inner and outer side bright yellow, horizontally flattened with funnel-shaped base, broadly obovate when spread out, 40–60 by +35–60 mm +, margin crenulate; stamen white with red dots, 20–27 by +8–11 mm +, apex yellow, anther +7–10 mm +long. +Capsule +ellipsoid, c. 12 by +6 mm +. +Seeds +c. 1.5 by +1 mm +. + + + + +Map 8 +Distribution of + +Costus lateriflorus +Baker. + + + + + +Fig. 5 + +Costus kupensis +Maas & H.Maas. + +a. Habit showing 2 basal inflorescences; b. leaves with ligules; c. bracteole, calyx and ovary; d. inflorescence with flower (a, b: +Cheek 7111 +, K; c: +Cable 2471, +K; d: after slide of +Cheek 7111 +). — Drawing by Hendrik Rypkema. + + + +Distribution — West Africa (Nigeria); Central Africa (Cam- eroon, Central African Republic, Equatorial Guinea, Gabon). + + + +Habitat & Ecology — In primary or sometimes secondary rainforest rich in +Caesalpinioideae +and + +Sacoglottis gabonensis + +, sometimes epiphytic on + +Baillonella toxisperma + +and + +Tetraberlinia bifoliolata + +, or on sandy to rocky soil, at elevations of + +0– +800 m. + +Flowering and fruiting: all year through. + + + + +IUCN Conservation Status — + +Costus lateriflorus + +occurs in about 17 locations with an AOO of +104 km +2 +. Six of these loca- tions have a protected status. Since we are unable to identify material of this species or + +C. lilaceus + +where the petal colour is not apparent, this species is likely to be more common than currently assessed. We therefore assess it as Least Concern ( +LC +). + + + + +Notes — + +Costus lateriflorus + +can be recognized by its mostly epiphytic habit, flowers with a bright yellow labellum and its inflorescences placed laterally in the axil of a leaf or terminating a separate leafless shoot. However, it is almost impossible to distinguish + +C. lateriflorus + +from + +C. lilaceus + +except for the strik- ing difference they show in the colour of their labellum: yellow in + +C. lateriflorus + +and lilac in + +C. lilaceus +. + +In the material studied we found +12 specimens +to be unidentifiable due to lack of information regarding flower colour on the label. The shoot of + +C. lateriflorus + +is brown (ligule) alternating with green (internodal part of the stem). The labellum of the flowers of + +C. letestui +Pellegr. + +, now in syn- onymy with + +C. lateriflorus + +, was described by Koechlin (1965, 1965) as being pink. However, the flowers of + +C. letestui + +are yellow, as in + +C. lateriflorus +Baker + +, because the label of the +type +specimen +Le Testu 1683 +( +P +) reads: ‘Epiphyte à fleurs jaunes’. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB2DFFE6FFCDFBA9FC2BFBE0.xml b/data/38/76/87/387687E2BB2DFFE6FFCDFBA9FC2BFBE0.xml new file mode 100644 index 00000000000..e8cb76729eb --- /dev/null +++ b/data/38/76/87/387687E2BB2DFFE6FFCDFBA9FC2BFBE0.xml @@ -0,0 +1,434 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +9. + +Costus giganteus +Welw. ex Ridl. + + +— +Plate 2c +; Map 6 + + + + + + +Costus giganteus +Welw. +ex +Ridl. (1887) + +131; K.Schum. (1904) 407. — +Type +: +Welwitsch 6465 +(holo +BM +2 +sheets [ +BM000617218 +, +BM000617219 +]; + + +iso +LISU +, +NY +), +São Tomé & Principe +, ‘ +Ilha de S. Thomé, Monte Caffé’ +, + +600– 850 m + +(‘2000–2800ft’), + +Dec. 1860 + + +. + + + + + +10. + +Costus gracillimus +Maas & H.Maas + + +, + +nom. nov. + +— +Plate 2d +; Map 6 + + + + + + +Costus gracillimus +Maas & H.Maas. + +— + +Costus pulcherrimus +A.Chev. (1917) + +304, nom. illeg., non Kuntze (1898) 301. — +Type +: +Chevalier 19568 +(holo +P +), +Ivory Coast +, +Tabou +, ‘ +Bassin du Cavally +, pays des +Tépos +, +entre Toula et Nekaougnié’ +, + +25 July 1907 + + +. + + + + +Terrestrial herb +1.5–8 m +tall. +Leaves +many; sheaths to c. +2 cm +diam; ligule chartaceous, truncate, +15–25 mm +long; petiole +15–30 mm +long; sheaths, ligule and petiole subglabrous; lamina shiny above, narrowly elliptic to narrowly obovate, rarely ovate, 28–52 by +7–16 cm +, upper side glabrous, lower side initially densely covered with soft, erect hairs +1–1.5 mm +long, soon glabrous, base acute to obtuse, apex acuminate (acumen +10–15 mm +long). +Inflorescence +many-flowered, ovoid, 12–20 by +7–10 cm +, terminating a separate leafless shoot 100–150(–300) cm long; bracts, bracteoles, calyx, ovary and capsule glabrous. +Flowers +1 per bract; bracts red, coriaceous, broadly ovate to ovate, 3.5–6 by +3–5 cm +, callus +5–10 mm +long; appendages absent; bracteole boat-shaped, +28–45 mm +long, callus (3–) +5–10 mm +long; calyx basally white, apically pinkish red, +13–25 mm +long, lobes shallowly ovate-triangular, 3–5(–7) mm long, callus absent; corolla yellow, +75–85 mm +long, glabrous, tube (25–) +35–40 mm +long, lobes narrowly elliptic, 40–45(–50) mm long, sometimes bending towards each other forming a kind of hood over the stamen; labellum completely yellow, tubular, narrowly elliptic to ovate when spread out, 40–45 by +15–20 mm +, lateral marginal parts curved upwards, upper margin crenulate; stamen erect, not bending downwards and not closing the throat, yellow, 40–50 by +5–10 mm +, apex cucullate, anther +10–12 mm +long. +Capsule +obovoid to subglobose, 15–20 by +10–20 mm +. +Seeds +3–3.5 by +2–2.5 mm +. + + + + +Terrestrial herb +1–3 m +tall. +Leaves +many; sheaths +0.2–0.6 cm +diam; ligule chartaceous, obliquely truncate, 10–15(–20) mm long; petiole +5–10 mm +long; sheaths, ligule and petiole glabrous or rarely sparsely covered with erect hairs < +1 mm +long; lamina greyish to brown on upper side, lower side paler, coriaceous, narrowly elliptic to elliptic, 13–21 by +4–8 cm +, slightly 4–6-pli- cate, glabrous on both sides, but margins and apex rarely covered with some hairs, base acute, apex acuminate (acumen +10–15 mm +long). +Inflorescence +few-flowered, broadly ovoid to globose, 1.5–5 by +1.5–5 cm +, terminating the leafy shoot; bracts, bracteoles, calyx, ovary and capsule glabrous, rarely rather densely covered with erect hairs < +1 mm +long. +Flowers +1(–2) per bract; bracts red, orange-red to red-purple, coriaceous, broadly ovate to ovate, 1.5–2.5 by +1.5–2.5 cm +, callus mostly absent or present and then c. +1 mm +long; appendages gener- ally absent; bracteole boat-shaped, +9–14 mm +long, callus +1–2 mm +long; calyx +7–10 mm +long, lobes very shallowly triangular, c. +1 mm +long, callus absent; corolla fleshy, +20–29 mm +long, red, orange or yellow, glabrous, tube +5–7 mm +long, lobes narrowly ovate to elliptic, +15–22 mm +long; labellum fleshy, red, orange or yellow, tubular, broadly obovate when spread out, 15–23 by +15–20 mm +, margin crenulate; stamen yellow, 13–15 by +6–8 mm +, anther +7–8 mm +long. +Capsule +obovoid, 9–10 by +5–6 mm +. +Seeds +1.5–2 by +1.5 mm +. + + + + +Distribution — Central Africa (both islands São Tomé and Principe and +one specimen +( +Wrigley & Melville 270 +) from Annobon (Equatorial Guinea)). + + + + +Habitat & Ecology — In rainforest. At elevations of +0– 1450 m +. Flowering and fruiting: October to January. + + + + +Field observations — Unlike most species of +Costus +, many flowers of the same inflorescence can be at anthesis at the same time. + + + + +IUCN Conservation Status — Based on an EOO of +3764 km +2 +and an AOO of +32 km +2 from three locations which all are only partially protected, while the remainder of these locations show severe habitat degradation (most records are actu-ally very old and the species has not recently been found in those localities), we assess this species as Endangered ( +EN +) B1ab(ii,iii)+2ab(ii,iii). + + + + +Notes — +Costus +giganteus +is unique among the African species of +Costus +by the combination of separate flowering shoots, combined with red bracts and yellow, tubular flowers. In these aspects it resembles some Neotropical species like +C. erythrocoryne +K.Schum. The only other African species of +Costus +with the same +type +of yellow, tubular flowers is + +C. +gracillimus, + +a species of much smaller stature from the African continent. The flowers of + +C. giganteus + +have a relatively narrow labellum with upcurved lateral margins and an erect cucullate stamen. The flower presents an open throat to pollinators, in contrast with all other species of African + +Costus + +where the single fertile stamen closes the throat and visitors have to force their way in. The filament is not flat but rolled inwards lengthwise along its margins, especially at its base. The corolla lobes bend towards each other forming a kind of hood over the stamen and the apex of the stamen is cucullate. This +type +of flower is unique to this species. The style of + +C. giganteus + +is often persistent after flowering. Young leaf lamina are shiny above, while older ones are dull green. The aril is relatively large, measuring up to 2 times the length of the seed. + + + +Distribution — West Africa (Ghana, Guinea, Ivory Coast, Liberia, Sierra Leone). + + + +Habitat & Ecology — Mostly in rainforest, along paths or in open places and/or disturbed areas, often in wet places, at elevations of + +0– +850 m. + +Flowering and fruiting: all year through. + + + + +IUCN Conservation Status — Based on all collections + +C. gracillimus + +has an AOO of +184 km +2 +from about 20 locations of which only four are partially protected, while the remainder of these locations are already lost or face severe habitat degradation. If we only use records collected since 1970, this species has only 10 locations left (with an +AOO +of +68 km +2 +), of which the majority is lost or threatened. We therefore assess this species as Vulnerable ( +VU +) A2; B2ab(i,ii,iii,iv,v). + + + + +Notes — + +Costus gracillimus + +is a relatively small herb with a slender spiralling shoot ( +0.2–0.6 cm +diam), a long ligule ( +10– 15 mm +long) and relatively small, tubular, fleshy flowers. The leaves of + +C. gracillimus + +have relatively narrow and long petioles. The labellum is about as long as the corolla, forming a tube with its longitudinally incurved margins. The majority of plants studied have red bracts with red-orange flowers. However, +Jongkind et al. 11941 +from Liberia has green bracts and yellow flowers. Based on the overall similarities of this single collec- tion, we do not believe it to be a separate species but rather a lighter-coloured form of + +C. gracillimus + +. + +Costus gracillimus + +has often been misidentified as + +C. deistelii +K.Schum. + +That species, known only from the +type +collection +Deistel 498 +( +B +destroyed), now placed in the synonymy of + +C. afer + +, differs from + +C. gracillimus + +by a shorter ligule, longer inflorescence and bracteole, and the presence of a rim at the base of the ligule not completely encircling the shoot. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB2EFFE5FFCDFBD2FBEDF98E.xml b/data/38/76/87/387687E2BB2EFFE5FFCDFBD2FBEDF98E.xml new file mode 100644 index 00000000000..f8714477da8 --- /dev/null +++ b/data/38/76/87/387687E2BB2EFFE5FFCDFBD2FBEDF98E.xml @@ -0,0 +1,464 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +7. + +Costus fenestralis +Maas & H.Maas + + +, + +sp. nov. + +— +Fig. 4 +; Map 6 + + + + + +Costus fenestralis + +can be recognized by a low number of obovate, densely hairy leaves concentrated at the top of the shoots and bracts soon falling apart into fibers. — + + + + + +Type +: +Jongkind et al. 5811 +(holo +WAG +2 +sheets [ +WAG0159192 +, +WAG0159193 +]; + + +iso +BR +, +K +, +LBV +[ +LBV0004878 +], +MO +, +UC +, WAG-spirit [ +WAG0115124 +]), +Gabon +, +Nyanga +, +Doudou Mountains +, +Chantier +SFN-Bakker, + +310 m + +, + +29 Nov. 2003 + + +. + + + + + +Etymology. +Costus fenestralis + +has been named for its bracts which have a ‘gauze-like’ appearance caused by the withering of the mesophyll tissue between the veins creating a net-like structure like in rotting old leaves.The same happens in the sheaths on the shoot creating bunches of long fibers around the shoot below the insertion of the leaves. + + + + +Terrestrial herb +0.5–1 m +tall. +Leaves +1–4, crowded in a rosette at the top of the shoot; sheaths +0.5–1.5 cm +diam, falling apart into separate fibers with age; ligule membranous, obliquely truncate to 1-lobed, +15–20 mm +long; petiole absent or up to c. +3 mm +long; sheaths, ligule and petiole densely covered with erect hairs < +1 mm +long to glabrous; lamina pale green on lower side, obovate, 22–35 by +10–15 cm +, slightly c. 20-plicate, upper side rather densely covered with appressed to erect hairs +0.5–2 mm +long, lower side densely so, base obtuse to cordate, apex acuminate (acumen +5–20 mm +long). +Inflorescence +many-flowered, ovoid, 5–8 by +3.5–5 cm +, terminating the leafy shoot; bracts and appendages on both sides densely covered with minute erect hairs < +1 mm +long, bracteoles with a row of hairs < +1 mm +long on the keel below the callus, calyx, ovary and capsule glabrous. +Flowers +1 per bract; bracts green, chartaceous, depressed ovate, 1.4–1.5 by +2 cm +, soon falling apart into separate fibers, callus sometimes present and then +1–2 mm +long; appendages green, reflexed, broadly ovate, 0.7–1 by +2 cm +; bracteole boat-shaped, +14–15 mm +long, callus c. +2 mm +long; calyx +13–15 mm +long, split on one side, lobes triangular, +2–5 mm +long, callus absent; corolla white, +40–60 mm +long, glabrous, tube c. +10 mm +long, lobes apically purplish, narrowly ovate, +30–50 mm +long; labellum lilac, inner side with a yellow nectar guide, horizontally flattened, broadly obovate when spread out, 50–60 by +50–60 mm +, margin crenate; stamen colour unknown, c. 30 by +10 mm +, anther +6–7 mm +long. +Capsule +and +seeds +not seen. + + + +Distribution — Central Africa (Angola (Cabinda), Congo Brazzaville, Gabon). + + + +Habitat & Ecology — In primary or secondary rainforest. At elevations of + +300– +650 m. + +Flowering and fruiting: November and December. + + + + +Field observations — The flowers of + +C. fenestralis + +have been reported to be slightly fragrant ( +Jongkind et al. 5811 +). + + + + +IUCN Conservation Status — Based on an AOO of +44 km +2 +from six locations of which only two are located in a protected area, while the others recently experienced logging or face several logging threats, we assess this species as Vulnerable ( +VU +): B2ab(ii,iii,iv). + + + + + + +Other +specimens +examined + +. +ANGOLA +. + +Cabinda + +, +Belize +, + +1 Jan.1919 + +, +Gossweiler 8232 +( +BM +). + +– + +CONGO BRAZZAVILLE +, + +Lékoumou + +, +Komono +, + +17 Jan. 1965 + +, +Bouquet 956 +( +P +); + + +Vouala Mongomo +, + +5 Feb. 1965 + +, +Bouquet 1198 +( +P +); + + +Route de M’bila +, +après le village Mouyabi +, + +12 Jan. 1968 + +, +Bouquet 2292 +( +P +). + +– + +GABON +, + +Ngounié + +, route +Malinga-Moukouagna +, +après village Nzinzi +, + +641 m + +, + +12 June 2011 + +, +Bissiengou 1319 +( +LBV +, +WAG +). + + + +Nyanga + +, route +Tchibanga-Mayumba +, + +19 Oct.2009 + +, +Bissiengou et al. 337 +( +WAG +); + + +Doudou Mts +, +Chantier +SNF-Bakker +, + +310 m + +, + +29 Nov.2003 + +, +Jongkind et al.5811 +( +LBV +, +WAG +); + + +Mouabissako +, + +8 Dec. 1907 + +, +Le Testu 1259 +( +BM +, +P +); + + +Forêt du Mayombe +, +Ndabiliba +(‘Dabiliba’), c. + +300 m + +, + +5 Feb. 1908 + +, +Le Testu 1299 +( +BM +, +P +); + + + +50 km +SSW of Doussala + +, + +480 m + +, + +14 Apr.1987 + +, +Reitsma et al.3230 +( +MO +, +NY +, +WAG +). + + +Ogooué-Maritime +, +Doudou Mts +, +Reserve de Faune de Moukalaba +, + +350 m + +, + +5 Dec. 1984 + +, +Arends et al. 651 +( +BR +, +MO +, +P +, +WAG +) + +. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB2EFFE6FC84F9C8FD29FBAE.xml b/data/38/76/87/387687E2BB2EFFE6FC84F9C8FD29FBAE.xml new file mode 100644 index 00000000000..f47b7525579 --- /dev/null +++ b/data/38/76/87/387687E2BB2EFFE6FC84F9C8FD29FBAE.xml @@ -0,0 +1,310 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +8. + +Costus gabonensis +Koechlin + + +— +Plate 2b +; +Map 7 + + + + + + +Costus gabonensis +Koechlin (1964) + +82, pl. 18, 1–5. — +Type +: +Le Testu 2240 +(holo +P +; + + +iso +A +, +B +, +BM +, +BR +, +G +, +K +, +L +[ +L.1480436 +], +P +), +Gabon +, +Ngounié +, +Tsamba +, + +27 Oct. 1917 + + +. + + + + +Terrestrial herb +0.5–2.5 m +tall. +Leaves +several; sheaths +0.5–1 cm +diam; ligule membranous, 2-lobed, +5–35 mm +long; petiole +2–5 mm +long; sheaths, ligule and petiole densely to sparsely covered with erect hairs to c. +5 mm +long; lamina green, some-times purple-red at lower side, shiny at upper side, narrowly elliptic, 13–28 by +5–9 cm +, upper side covered with stiff, erect hairs +1.5–2 mm +long to glabrous, lower side sparsely to rather densely covered with soft erect hairs c. +1.5 mm +long, base acute, obtuse to subcordate, apex acuminate (acumen +5–10 mm +long). +Inflorescence +many-flowered, ellipsoid to ovoid, 5–9 by +2–4 cm +, terminating a leafy shoot; bracts, appendages of bracts, bracteoles, calyx, ovary and capsule densely to rather densely covered with erect to appressed, white hairs < +1 mm +long. +Flowers +1 per bract; bracts white at base, greenish pink to red or purplish brown at apex, chartaceous, broadly obovate to obovate, 1–1.5 by +0.5–1.5 cm +, callus absent; appendages pinkish red to purplish brown, strongly reflexed, narrowly trian-gular to triangular, 1–3 by +0.6–1.5 cm +; bracteole boat-shaped +15–20 mm +long, callus green, +1–3 mm +long; calyx +9–10 mm +long, lobes deltate to very shallowly triangular, +1.5–3 mm +long, callus absent; corolla yellow to dark yellow, +40–50 mm +long, densely to rather densely covered with (erect to) appressed, white hairs < +1 mm +long, tube +10–20 mm +long, lobes narrowly elliptic, 20–30(–40) mm long; labellum completely yellow, hori-zontally flattened, broadly obovate when spread out, 35–50 by +40–50 mm +, margin irregularly lobed; stamen yellow, 35–40 by +7–10 mm +, apex slightly orange, anther +7–8 mm +long. +Capsule +obovoid, 9–10 by +6–7 mm +. +Seeds +c. 3 by +2 mm +. + + + + +Fig. 4 + +Costus fenestralis +Maas & H.Maas + +a. Habit showing few leaves in an apical rosette; b. detail of sheaths dilacerating into fibers; c. detail of withered bract; d. detail of bracteole and calyx; e. inflorescence (all: +Jongkind et al. 5811, +WAG). — Drawing by Hendrik Rypkema. + + + +Distribution — Central Africa (Gabon). + + + +Habitat & Ecology — In primary and secondary rainforest, at elevations of +300–1000 m +. Flowering and fruiting: September to December. + + + + +Field observations — The flowers of this species are quite aberrant from any other species of + +Costus + +in that they emit a strong scent reminiscent of jasmine ( +A.M. Louis et al. 853 +, +Van Valkenburg et al. 2649 +). + + + + +IUCN Conservation Status — Based on an AOO of +88 km +2 +from about 14 locations of which only two are located in a protected area, while the others are located in areas currently being logged or face logging threats, we assess this species as Near Threatened ( +NT +). + + + + +Plate 2 +a. + +Costus dubius +(Afzel.) K.Schum. + +Basal inflorescence. – b. + +Costus gabonensis +Koechlin. Inflorescence. + +– c. + +Costus giganteus +Welw. ex Ridl. + +Inflo- rescence. – d. + +Costus gracillimus +Maas & H.Maas. Inflorescence + +with red bracts (a: photographed in Burgers’ Bush, Arnhem, The Netherlands, no specimen collected; b: +Maas et al. 10465 +; c: +Scharf 221 +; d: +Maas et al. 10571 +). — Photos: a, b, d: P.J.M.Maas; c: L.Y.T.Westra. + + + + +H. Maas-van de Kamer et al.: Monograph of African +Costaceae + + +299 + + + + +Map 7 +Distribution of + +Costus gabonensis +Koechlin + +(●) and + +C. loangensis +H.Maas & Maas + +(■ + + +). + + +Notes — + +Costus gabonenis + +is unique by its combination of bracts with reflexed red to purplish brown appendages, yellow flowers and a densely hairy corolla. It is endemic to Gabon and it superficially resembles the Neotropical + +C. comosus +(Jacq.) Roscoe. + +The boat-shaped bracteole of + +C. gabonensis + +is 2-keeled to almost 2-winged presumably caused by the compactness of the inflorescence. The base of the shoot is red or purplish brown. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB30FFFAFC84FBCEFE6AF965.xml b/data/38/76/87/387687E2BB30FFFAFC84FBCEFE6AF965.xml new file mode 100644 index 00000000000..b006fe9cff3 --- /dev/null +++ b/data/38/76/87/387687E2BB30FFFAFC84FBCEFE6AF965.xml @@ -0,0 +1,322 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +5. + +Costus dinklagei +K.Schum. + + +— +Plate 1d +; +Map 4 + + + + + + +Costus dinklagei +K.Schum. (1904) + +408. — Type: +Dinklage 987 +(holo +B +de-stroyed), +Cameroon +, +South Province +, +Gross-Batanga. As +the holotype at +Berlin +was destroyed and no other original material has been located, + + +we hereby select a +neotype +from a locality not far from the type locality: + +Van Andel +et al.3549 + +(neo +WAG +2 +sheets [ +WAG0146035 +, +WAG0380166 +] + +; + +isoneo +KRIBI +, +SCA +, +U +[ +U0064546 +], WAG-spirit [ +WAG0028342 +], +YA +), +Cameroon +, +South Province +, +Mont d’Ėléphant +, +road Bidou-Akom II +, foot of the hill, + +23 m + +, + +10 June 2001 + + +. + + + + +Terrestrial herb +1–3 m +tall. +Leaves +many; sheaths 0.5–2.5(–3) cm diam; ligule chartaceous, truncate, +10–20 mm +long; petiole +3–10 mm +long; sheaths, ligule and petiole hairy as the lower side of the leaves; lamina narrowly elliptic, sometimes narrowly obovate, 15–40 by +5–13 cm +, upper side glabrous, lower side densely to sparsely covered with erect to appressed brown hairs +0.5–2 mm +long, base acute, apex acuminate (acumen +15–40 mm +long). +Inflorescence +many-flowered, ovoid to ellipsoid, 4–15 by +2.5–6 cm +, terminating a separate leafless shoot +5–30 cm +long, rarely terminating a leafy shoot; bracts, bracteoles, calyx, ovary and capsule densely covered with erect hairs < +1 mm +long. +Flowers +1 per bract; bracts green to dark green, sometimes reddish, coriaceous, broadly ovate-elliptic, 1.5–5.5 by +1–3.5 cm +, callus +1–2 mm +long; appendages ab-sent; bracteole boat-shaped, +16–35 mm +long, callus +3–4 mm +long; calyx +12–20 mm +long, lobes shallowly to broadly ovatetriangular, +2–6 mm +long, callus +1–2 mm +long; corolla hyaline, white to pale pinkish, +45–55 mm +long, glabrous, tube +15–20 mm +long, lobes narrowly elliptic, +30–40 mm +long; labellum at the outer side white to (pale)pink, inner side white to pink with darker coloured margin and often pale yellow nectar guide, funnel-shaped, broadly obovate when spread out, 40–60 by +30–50 mm +, margin crenate or undulate, fimbriate; stamen white, 20–35 by +10–13 mm +, apex pink, anther +6–7 mm +long. +Capsule +not seen. +Seeds +c. 2 by +1 mm +. + + + +Distribution — West Africa (Nigeria); Central Africa (Cameroon, Equatorial Guinea, Gabon). + + + + + + + + + + + + + + + + + + + +
+ +H. Maas-van de Kamer et al.: Monograph of African + +Costaceae + + +
(((! (! (! (! (
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+ + + + +
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(
+ + + +Map 5 +Distribution of + +Costus dubius +(Afzel.) K. Schum. + + + + + + + +Map 4 +Distribution of + +Costus dinklagei +K. Schum. + +(●) and + +C. ligularis +Baker + + + +(■). + + + + + +Habitat & Ecology — In rainforest, often near streams or in wet places, on clay soil, at elevations of +0–1100 m +. Flowering and fruiting: from March to July and in December. + + + +IUCN Conservation Status — Near Threatened. + + + +Notes — + +Costus dinklagei + +can be recognized by its inflorescence terminating a separate leafless shoot with 1-flowered bracts and hyaline whitish erect corolla lobes. The labellum is white to pale pink with yellow nectar guide, basally funnelshaped but with the upper part horizontally flattened. The lower side of the leaf lamina, the sheaths and the petioles are hairy. The apex of the stamen of + +C. dinklagei + +is narrowly triangular (Hallé 1967). + +Costus dinklagei + +can be confused with + +C. dubius + +both having a basal inflorescence with green, unappendaged bracts, but + +C. dinklagei + +has hyaline, whitish corolla lobes and a white to pale pink labellum with yellow nectar guide and dark pink margin, whereas in + +C. dubius + +the white corolla lobes are not hyaline and the labellum is white with only a yellow nectar guide. Moreover, in + +C. dinklagei + +the lower side of the lamina, the petioles and the sheaths are distinctly hairy, while all vegetative parts are glabrous in + +C. dubius + +. + + +
+
\ No newline at end of file diff --git a/data/38/76/87/387687E2BB31FFE5FFCDF8DDFD6BFC68.xml b/data/38/76/87/387687E2BB31FFE5FFCDF8DDFD6BFC68.xml new file mode 100644 index 00000000000..efb75e18cbd --- /dev/null +++ b/data/38/76/87/387687E2BB31FFE5FFCDF8DDFD6BFC68.xml @@ -0,0 +1,406 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +6. + +Costus dubius +(Afzel.) K.Schum. + + +— +Plate 2a +; +Map 5 + + + + + + +Costus dubius +(Afzel.) K.Schum.(1904) + +409. — + +Zingiber dubium +Afzel.(1813) + +9. — Type: +A collection by Afzelius, +Sierra Leone +, without location.As no original material of Afzelius could be traced we here designate the follow-ing +neotype +from the same country: +Pyne 88 +(neo +K + +; + +isoneo +P +), +Sierra Leone +, +Moyamba District +, +Kori Chiefdom +, +Gbonjema +, (‘ +Bonjema +( +Kori +)’), + +21 Dec. 1955 + + +. + + + + + + +Costus maculatus +Roscoe (1825) + +218,pl. 82; +K.Schum +. (1904) 408. — + +Costus afer +var. +maculatus +(Roscoe) Baker (1898) + +299, syn. nov. — +Type +: +Roscoe’s plate 82 +(1825) + +. + + + + +Costus littoralis +K.Schum. (1904) + +395. — +Type +: +Dinklage 1701 +(holo +B +), +Liberia +, +Grand Bassa +, near +Fishtown +, + +14 Aug. 1896 + + +. + + + + +Costus albus +A.Chev. (1920) + +627 (for the status of this name see the notes under + +C. aureus + +). — +Type +: +Chevalier 15217 +(lecto +P +, designated here; + + +isolecto +LY +), +Ivory Coast +, +Bingerville region +, +Abidjan +, +Dabou +, + +19 Mar. 1905 + +; + + +other +syntype +: +Chevalier 17579 +( +P +), +Ivory Coast +, lower +Comoé River +, Bettié, + +15–17 Mar. 1907 + + +. + + + + +Terrestrial herb +0.5–3 m +tall. +Leaves +many; sheaths +0.5–2 cm +diam; ligule chartaceous, truncate to 2-lobed, (3–)5–20(–30) mm long; petiole (3–)10–20(–25) mm long; sheaths, ligule and petiole generally glabrous; lamina shiny above, more or less succulent, narrowly elliptic,15–36 by (4–) +6–12 cm +, upper side glabrous, lower side glabrous, margin often with a row of hairs < +1 mm +long, base acute, obtuse, or cordate, apex acuminate (acumen +10–30 mm +long). +Inflorescence +many-flowered, ovoid to ellipsoid or narrowly so, 5–20(–30) by +3–6 cm +, terminat-ing a separate leafless shoot 5–40(–100) cm long, or rarely terminating the leafy shoot; bracts, appendages of bracts, bracteoles, calyx, ovary and capsule glabrous, except for some erect hairs < +1 mm +long at the base of the calyx and apex of the ovary. +Flowers +1 per bract, rarely 2; bracts green with reddish margins, sometimes becoming red in fruit, coriaceous, bulging, very broadly ovate, 1.5–3 by +2–3.5 cm +, callus sometimes pre-sent and then to c. +2 mm +long; appendages generally absent; bracteole boat-shaped, +20–25 mm +long, callus +2–3 mm +long; calyx +12–18 mm +long, lobes broadly ovate-triangular to deltate, +3–5 mm +long, callus very inconspicuous; corolla white to cream, +25–55 mm +long, glabrous, tube +12–15 mm +long, lobes narrowly elliptic, +25–40 mm +long; labellum white, inner side with central yellow nectar guide, funnel-shaped, broadly obovate when spread out, 35–40 by +30 mm +, margin crenate; stamen white, 25–30 by +8–9 mm +, anther +6–8 mm +long. +Capsule +ellipsoid to obovoid, 10–15 by +6–12 mm +. +Seeds +2–2.5 by +1.5 mm +. + + + +Distribution — North East Africa (South Sudan); West Africa (Burkina Faso, Ghana, Guinea, Ivory Coast, Liberia, Nigeria, Senegal, Sierra Leone, Togo); Central Africa (Burundi, Cam-eroon, Central African Republic, Congo Brazzaville, Congo Kinshasa, Equatorial Guinea, Gabon); East Africa (Kenya, Tanzania, Uganda); Southern Tropical Africa (Angola, Malawi, Mozambique). + + + +Habitat & Ecology — In primary rainforest, savanna forest, coastal forest, secondary forest, or swamp forest, in shady places, also along roads and rivers and in plantations, on clayish soil at elevations of +0–1400 m +. Flowering and fruiting: all year through. + + + + +Field observations — + +Costus dubius + +plants are the only cultivated species of + +Costus + +often setting seed in greenhouses. Their seedlings germinate easily and tend to take over other pots with different species of + +Costus + +growing beside them. + + + +IUCN Conservation Status — Least Concern. + + + +Notes — + +Costus dubius + +can be recognized by its inflorescence generally near the base of the plant terminating a separate leafless shoot, inflorescence composed of 1-flowered green unappendaged bracts and flowers having a white labellum with a yellow nectar guide. The leaves of this species are glabrous and the shoot is often covered by reddish dots. For the differences between + +C. dubius + +and + +C. afer + +see under + +C. afer + +. For the differences between + +C. dubius + +and + +C. dinklagei + +, see under + +C. dinklagei + +. + +Of the +two +syntypes +of + +C. trachyphyllus + +(now in the synonymy of + +C. afer + +) +Schweinfurth 3268 +( +B +destroyed, +K +), from +South Sudan +, +Western Equatoria +, ‘ +am Turu bei Uando’s Dorf’ +, + +10 Mar. 1870 + +, probably belongs to + +C. dubius + +, because of its white flowers mentioned on the label (‘fl. albo’) + +. As in many species of + +Costus + +, inflorescences are generally terminating a leafless shoot but can (rarely) terminate a leafy shoot. Plants with both +types +of inflorescences have both been included in the description. Some specimens of + +C. dubius + +do have a very long ligule (1-lobed or obliquely truncate, acute, +25–30 mm +long). These specimens are: +Breteler 1209 +from +Cameroon +, +Ekwuno 12 +from +Nigeria +and +Harris 3211 +from +Congo +. The collection by +Friedmann 3919 +has been found East of the African continent on the Seychelles, on the island of Mahé. Because on the label is written: ‘subspontanée’, we suppose this collection might not represent a natural distribution. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB33FFF8FC84FEBBFA81F8FC.xml b/data/38/76/87/387687E2BB33FFF8FC84FEBBFA81F8FC.xml new file mode 100644 index 00000000000..f040fd53ab0 --- /dev/null +++ b/data/38/76/87/387687E2BB33FFF8FC84FEBBFA81F8FC.xml @@ -0,0 +1,365 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +6c0dbc52-820c-4f68-912d-1bcaa2227efc +7570023 + + + + + +3. + +Costus albiflos +Maas & H.Maas + + +, + +sp. nov. + +— +Plate 1c +; +Map 2 + + + + + +Costus albiflos + +is very easily recognizable by its leafless flowering shoot, green appendaged bracts and completely white flowers (with only a slightly yellow nectar guide). Its petiole, ligule and sheaths are covered with ap-pressed, +0.5–1 mm +long hairs with a thickened base creating a ‘rough’ feeling. — + + + + + +Type +: +Maas et al. 10411 +(holo +WAG +2 +sheets [ +WAG0380170 +, +WAG0380171 +]; + + +iso +BR +, +K +, +L +[ +L.2079937 +], +LBV +, +MO +, +P +, +UC +), +Gabon +, +Estuaire +, +side road at km 46 of road from Kougouleu to Méla +, on the border of +Parc National Monts de Cristal +, + +15 m + +, + +21 Nov. 2011 + +. + + + + + +Terrestrial herb +1–3 m +tall. +Leaves +many; sheaths +1–1.5 cm +diam; ligule chartaceous, 2-lobed, +10–30 mm +long; petiole +5–10 mm +long; sheaths, ligule and petiole rather densely covered with appressed hairs < +1 mm +long; lamina pale green below, narrowly elliptic to narrowly obovate, 20–40 by +5–8 cm +, slightly 6 –10-plicate, upper side glabrous or sparsely covered with appressed hairs < +1 mm +long, lower side sparsely covered with appressed hairs < +1 mm +long to glabrous, midrib rather densely so and hairs longer, base acute, apex acuminate (acu-men +15–20 mm +long). +Inflorescence +many-flowered, ovoid, 4–12 by +3–8 cm +, terminating a separate leafless shoot +10–50 cm +long; bracts, appendages of bracts, bracteoles and calyx sparsely covered with appressed hairs < +1 mm +long, ovary and capsule glabrous. +Flowers +1 per bract; bracts green, coriaceous, broadly ovate, 1.5–2 by +1–2.5 cm +, callus absent; append-ages green, horizontally spreading, broadly ovate-triangular to ovate-triangular, 1–3.5 by +1–2.5 cm +; bracteole boat-shaped, 18–20(–25) mm long, with 1 or 2 calli +1–1.5 mm +long; calyx +9–14 mm +long, lobes ovate-triangular, +2–4 mm +long, callus absent; corolla white, +50–55 mm +long, glabrous, tube c. +15 mm +long, lobes narrowly ovate, +35–40 mm +long; labellum white, inner side sometimes with a pale yellow nectar guide, horizon-tally flattened, broadly obovate when spread out, 30–35 by +30 mm +; stamen white, 30–40 by +10 mm +, anther 5–6(–9) mm long. +Capsule +ellipsoid, 10–15 by +6–8 mm +. +Seeds +1–2 by +1–2 mm +. + + + +Distribution — Central Africa (Cameroon, Gabon). + + + +Habitat & Ecology — In lowland rainforest, often near streams, at elevations of + +0– +700 m. + +Flowering and fruiting: February, April and May. + + + + +IUCN Conservation Status — Based on an AOO of +40 km +2 +from seven locations of which only one is part of a National Park, while most others face several logging threats, we assess this species as Vulnerable ( +VU +): B2ab(ii,iii,iv). + + + + + +Other specimens examined +. +CAMEROON +, + +South Province + +, Collines BOG, +5 km +W of Atogboga ( +25 km +NNE +of Bipindi), +30 Jan. 1974 +, +Letouzey 12829 +( +P +) + +; + +Colline Nkol Tsia, +18 km +NW of Bipindi, near Gouap, +488 m +, +5 Feb. 1974 +, +Letouzey 12913 +( +P +) + +; + +Nyangong, transect +8, 700 m +, +12 Dec. 1996 +, +Van Gemerden 101 +( +WAG +) + +. + + +South-West Province + +, Ndian, Ekundu Kundu, +200 m +, +26Apr.1996 +, +Cheek et al. 8204 +( +K +, +WAG +) + +. + + +GABON +, +Estuaire +, Crystal Mountains, +3 km +along track Alen Nkomo-Andok Foula, +30 m +, +21 Nov. 1986 +, +J.J.F.E +. +de Wilde et al. 8895 +( +LBV +, +MO +, +WAG +) + +; + +Parc National de Monts de Cris-tal, road L108 from Kinguélé to Tchimbélé, past Kinguélé, c. +300 m +, +24 Oct. 2011 +, +Maas et al.9968 +( +LBV +, +WAG +) + +. + +Woleu-Ntem +, Chantier Oveng,c. +500 m +, +7 May 1986 +, +A.M. Louis 2185 +( +LBV +, +WAG +) + +; + +Crystal Mountains, +1 km +S of Tchimbélé, +450 m +, +14 Nov. 2004 +, +Wieringa et al. 5423 +( +WAG +) + +. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB33FFFBFC84F878FB0DFB95.xml b/data/38/76/87/387687E2BB33FFFBFC84F878FB0DFB95.xml new file mode 100644 index 00000000000..6863abb2f17 --- /dev/null +++ b/data/38/76/87/387687E2BB33FFFBFC84F878FB0DFB95.xml @@ -0,0 +1,897 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +6c0dbc52-820c-4f68-912d-1bcaa2227efc +7570023 + + + + + +4. + +Costus aureus +Maas & H.Maas + + +, + +sp. nov +. + +— +Plate 1b +; +Map 2 + + + + + +Costus aureus + +is characterized by flowers that are completely yellow and arranged in an inflorescence terminating a leafy shoot and composed of green and generally appendaged bracts. Vegetatively it looks very similar to + +C. lucanusianus + +by having a rim at the base of the ligule.However, this rim is hairless in + +C. aureus +, + +while it is distinctly hairy in + +C. lucanusianus + +. — + + + + + +Type +: +Berg 186 +(holo +U +4 +sheets [ +U +0123675, +U +0123676, +U +0123677, +U +0123678]; + + +iso +B +, +MO +, +NY +), +Ivory Coast +, near +Akoupé +( +NW of Abidjan +), + +31 July 1972 + + +. + + + + + + +Costus luteus +A.Chev. (1920) + +628, nom. illeg. non Blanco (1837) 4. — +Type +: +Chevalier 17125 +(lecto +P +,designated here), +Ivory Coast +,‘ +Vallée de l’Agniéby à Guébo’ +, + +31 Jan.1907 + + +; + +other +syntype +: +Chevalier 17454 +( +LY +, +P +), +Ivory Coast +, Attié, near Alépé, +26–28 Feb. +to +1–3 Mar. 1907 + +. + + + + +Terrestrial herb +0.5–3 m +tall. +Leaves +many; sheaths +0.5–3 cm +diam; ligule chartaceous, truncate, 1–5(–8) mm long, with a prominent glabrous rim at its base; petiole +5–18 mm +long; sheaths, ligule and petiole sparsely to rather densely covered with erect to appressed hairs < +1 mm +long; lamina shiny on both sides, lower side dull greyish green, narrowly elliptic, rarely narrowly obovate, 15–30 by +4–8 cm +, slightly plicate, margins often somewhat undulate, upper side sparsely covered with appressed hairs < +1 mm +long (mainly along midrib) to glabrous above, lower side sparsely to rarely rather densely covered with appressed hairs < +1 mm +long, base acute, the very base sometimes somewhat rounded, apex acuminate (acumen +5–20 mm +long), sometimes acute. +Inflorescence +many-flowered, very broadly to depressed ovoid to subglobose, 3.5–7 by +4–8 cm +, terminating the leafy shoot; bracts, appendages of bracts, bracteoles, calyx, ovary and capsule sparsely to rather densely covered with erect hairs < +1 mm +long to glabrous. +Flowers +2 per bract; bracts green, coriaceous, broadly ovate, 1.5–2.5 by +1–2.5 cm +, sometimes falling apart into separate fibers with age, callus absent; appendages mostly present, green, ascending, broadly ovate-triangular, 1–1.5 by +1–2 cm +; bracte-ole boat-shaped, +15–20 mm +long, callus +2–3 mm +long; calyx +15–25 mm +long, in fruit exceeding the bracts, lobes triangular, +2–7 mm +long, callus absent; corolla yellow, +30–40 mm +long, glabrous, tube c. +10 mm +long, lobes narrowly elliptic, +20–30 mm +long; labellum yellow, inner side with darker yellow nectar guide, horizontally flattened, broadly obovate when spread out, 40–45 by +35–40 mm +; stamen yellow, c. 25 by +8 mm +, apex darker yellow, anther +7–8 mm +long. +Capsule +ellipsoid, 10–12 by +4–6 mm +. +Seeds +1.5–2 by +1–1.5 mm +. + + + +Distribution — West Africa (Ghana, Ivory Coast, Liberia). + + + +Habitat & Ecology — In primary or secondary rainforest, often in wet places, on clay to sandy soil, at elevations of + +0 – +600 m. + +Flowering and fruiting: all year through. + + + +IUCN Conservation Status — Least Concern. + + + + +Selected specimens examined. +GHANA +, + +Ashanti Region +, + + + +Distr. Sefwi Wiawso +, Anhwiaso + + +Forest Reserve +, +1 Sept. 1984 +, +Andoh FH 5241 +( +K +) + +; + +10 miles +S of Mampon(g), +8 Dec. 1953 +, +Morton GC 9675 +( +K +) + +; + +Fumso, +24 Mar. 1950 +, +Obeng-Darko 545 +( +K +) + +. + +Central Region, +Wassa Atobiase,road to Rock Shrine, +70 m +, +21 July 2010 +, + +Van Andel +5769 + +( +GC +, +WAG +) + +. + + +Western Region + +, Elubo, +22 km +ESE towards Takoradi, +80 m +, +14 July 1995 +, +Harder 3435 +( +K +, +MO +) + +; + +Ankasa Game Reserve near entrance, +100 m +, +28 Feb. 1995 +, +Jongkind 2072 +( +MO +, +WAG +) + +; + +Ankasa River + + +Forest Reserve +, along dirt road to centre of reserve, +60 m +, +30 July 2010 +, + +Van Andel +5865 + +( +GC +, +L +, +U +, +WAG +) + +. + + +IVORY COAST +, +Banco Forest Reserve +, +25 July 1975 +, + +W. +J. van +der Burg 673 + +( +BR +, +FR +, +MO +, +UCJ +, +WAG +) + +; + +Vallée de l’Agneby à Guébo, +31 Jan.1907 +, +Chevalier 17125 +( +P +) + +; + +pays de l’Attié, Alepe, +25 Feb. 1903 +, +Chevalier 17454 +( +LY +, +P +) + +; +Banco + +Forest Reserve +, +11 Dec. 1972 +, +De Koning 887 +( +BR +, +E +, +MO +, +WAG +) + +; + +km 25–30 on new road Abidjan-Ndouci, +21 Aug. 1979 +, +De Kruif 305 +( +UCJ +, +WAG +) + +; + +Forêt de l’Angedédou +, c. +15 km +NW of + + +Abidjan +, +40 m +, +3 Nov. 1958 +, +Leeuwenberg 1874 +( +BR +, +F +, +K +, +UC +, +WAG +) + +; + +Forêt l’Anguédodou near Adiopodoumé, +25 Dec. 1957 +, +H.C.D. de Wit 7850 +( +WAG +) + +. + +Aboisso, +2 km +E of Maféré, near road to Afiénou, +50 m +, +18 June 1975 +, +Beentje 447 +( +AMD +, +UCJ +, +WAG +) + +; + +12 km +SE of Aboisso, +25 July 1968 +, +Breteler 5297 +( +WAG +) + +. + +Adzopé +, SOFALCO planta-tions, +2 km +S of Adzopé, +100 m +, +14 Dec. 1972 +, +Leeuwenberg 10716 +( +WAG +) + +; + +Aouabo, +16 May 1969 +, +Thijssen 21 +( +WAG +) + +. + +Agboville + +, + +Forêt de +la Mambo, lisière Est de la forêt de Mambo, piste Albéric, +28 Jan. 1992 +, +Chatelain 962 +( +CSRS +, +WAG +) + +; + +Gare des Makaugnié, Chemin de fer km 75, +22 Jan. 1907 + +, + + +Chevalier +16951 + +( +P +) + +; + +Foret d’Yapo, +9 Oct. 1957 +, +Farron s.n. +( +G +) + +. + +Danané, +Danipleu region, +27 Mar. 1982 +, +César 1716 +( +P +) + +; + +20 km +N of Danané, +18 Dec. 1967 +, +Geerling 1862 +( +WAG +) + +. + +Guiglo +, route de + + +Tabou +, near Siéblo Oula, +29 Dec. 1985 +, +Aké Assi 17212 +( +G +, +MO +) + +; + +Forêt de Tai +, near station, +21 Nov. 1982 +, +C.C. Berg 1460 +( +U +) + +; + +Tienkoula, +4 Aug. 1962 +, +Jangoux 255 +( +BR +) + +. + +Man, +F.C. Scio, Pinhou, Lobykro, +2 Sept. 2001 +, +Nusbaumer 693 +( +G +) + +. + +Sassandra +, Along road from Dakpadou to Sago, N of + + +Sassandra +, +30 Mar. 1968 +, +Geerling 2352 +( +WAG +) + +; +on border of + +River Niegré +, c. +64 km +N of + + +Sassandra +near vil-lage Baléko, +16 June 1963 +, +W.J.J.O. de Wilde 254 +( +WAG +) + +. + + +Tabou + + +, + +Tabou +campment, +4 Sept. 1975 +, + +W. +J. van +der Burg 930 + +( +WAG +) + +. + + +LIBERIA +, +Grand Gedeh +, east slope of the Putu Hills East Range west of Tiama Town, +240 m +, +25 May 2005 +, +Jongkind 6379 +( +WAG +) + +; + +Putu Hills, East ridge, +628 m +, +29 Sept. 2013 +, +Jongkind 12192 +( +WAG +) + +. + +Maryland +, +Webo District +, Nyaake, +24 June 1947 +, +Baldwin 6126 a! +( +K +) + +. + +Montserrado +, Firestone Plantation along Dukwai R., +170 m +, +1 Nov. 1928 +, +G.P. Cooper 14 +( +BM +, +F +, +GH +, +K +, +NY +, +P +, +US +) + +; + +New University Site, +30 km +from + + +Monrovia +, +27 Sept. 1963 +, +Harten 127 +( +WAG +) + +; + +Road Monrovia +to Kakata, c. +13 miles +from + + +Monrovia +,near Mount Barclay, +1 Feb. 1966 +, +Van Meer 349 +( +WAG +) + +. + +Sino, +road from Greenville to African Fruit Company, +27 July 1977 +, +De Gier 13 +( +WAG +) + +; +Sapo NP, buffer zone, around Safari Camp on short distance of + +Sinoe River +, +115 m +, +22 Nov.2002 +, +Jongkind 5274 +( +BR +, +G +, +WAG +) + +; + +near Jalay’s Town, +29 Jan. 2016 +, +Jongkind 12849 +( +BR +) + +. + + + + +Note — + +Costus luteus +A.Chev. + +has a doubtful status. The introduction of the work in which it was published (Chevalier 1920) states that new names in that work are only mentioned and will be described later, but it is clear that they are nevertheless accepted, so art. 36.1 of the +ICBN +(McNeill et al. 2012) does not apply. However, often the names of this work are also not considered as validly published because the descriptions it contains are not recognized as such. But Chevalier often copies his own field descriptions when citing the specimens, which we consider as validating descriptions. In the case of + +C. luteus + +the name, when considered validly published, is a later homonym of + +C. luteus +Blanco + +(nowadays + +Roscoea lutea +(Blanco) Hassk. + +), and cannot be used in any case. However, to circumvent any discussion about the validity of Chevalier’s publication, we describe this species here independently as new and refrain from only using the nom. nov. construction. Because the name + +C. luteus + +had already been used, we name this yellow-flowered species + +C. aureus +. + + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB34FFF8FC8BFB78FB70FE83.xml b/data/38/76/87/387687E2BB34FFF8FC8BFB78FB70FE83.xml new file mode 100644 index 00000000000..251df5a49cf --- /dev/null +++ b/data/38/76/87/387687E2BB34FFF8FC8BFB78FB70FE83.xml @@ -0,0 +1,700 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + +2. + +Costus afer +Ker Gawl. + + +— +Plate 1a +; +Map 3 + + + + + + +Costus afer +Ker Gawl. (1823) + +t. 683; K.Schum. (1904) 392. — +Type +: + +A +specimen +from cultivated material in the greenhouses of the Horticultural Society at London (Chelsea) from material collected in +Sierra Leone +by +G. Don + +(holo +CGE +) + +. + + + + + + +Costus sarmentosus +Bojer (1835) + +262, t. 8; K.Schum. (1904) 394, syn. nov. — Type ( +lectotype +selected by Lock (1985: 7): +Bojer (1835) plate 8 +, drawn from a plant from + +Zanzibar + + +. + + + + +Costus trachyphyllus +K.Schum. (1892) + +420; (1904) 409, syn. nov. — +Type +: +Schweinfurth ser. III, n. 206 +(lecto +K +, selected by Lock (1984) 842), +Congo Kinshasa +, +Orientale +, +Mbrwole River +(‘bei +Mruole +am Nabambisso’), + +1 Mar. 1870 + + +. + + + + +Costus edulis +De Wild.& T.Durand + +in Durand & De Wildeman (1899) 141. — +Type +: +Dewèvre 916a +(holo +BR +), +Congo Kinshasa +, +Nyangwe +, +Mossungulore +, anno 1896 + +. + + + + +Costus oblitterans +K.Schum. (1904) + +393, syn. nov. — +Syntypes +: +Unknown collector s.n. +( +B +destroyed), +Ghana +(‘Goldcoast’), without location + +; + +Millen s.n. +( +B +destroyed), +Nigeria +, +Lagos + +. + + + + +Costus deistelii +K.Schum.(1904) + +393,syn. nov. — +Type +: +Deistel 498 +(holo +B +destroyed), +Cameroon +, +South-West Province +, +Buea +, + +Feb. 1900 + + +. + + + + +Costus subbiflorus +K.Schum.(1904) + +394,syn.nov. — +Type +: +Volkens 50 +( +B +de-stroyed; + + +lecto +BM +, designated here), +Tanzania +, +Lushoto Distr +., ‘ +Usambara +, von +Derema bis Magila +(‘Msassaberg’), +häufig im Urwald z. B. bei Punga Ninga’ +, + +900 m + +, + +21 Jan. 1893 + + +; + +other +syntypes +: +Engler 715 +( +B +destroyed), +Tanzania +, ‘ +Usambara’ +, +Amani +, + +800–900 m + +, + +Nov. 1902 + + +; + +Buchwald 360 +( +B +destroyed), +Tanzania +, ‘ +Usambara’ +, +Mt Lutindi between Kwa Mburaka and Kisula +, + +19 Jan. 1896 + + +; + +Liebusch 17 +( +B +destroyed), +Tanzania +, ‘ +Usambara’ +, +Tanga +, Pamota, +800–1000 m +, +15 Mar. 1900 + +. + + + + +Costus pterometra +K.Schum. (1904) + +394, syn. nov. — +Type +: +Schweinfurth III-204 +(holo +B +destroyed; + + +lecto +K +2 sheets,designated here), +South Sudan +, ‘ +Ghasaquellengebiet +, +Land der Niamniam am Nabambisso’ +, + +20 Feb. 1870 + + +. + + + + +Costus anomocalyx +K.Schum. (1904) + +396, syn. nov. — +Type +: +Baumann 8 +(holo +B +destroyed), +Togo +, ‘ +Misahöhe +, + +496 m + +ü. M.’, + +15 Mar. 1894 + + +. + + + + +Costus megalobractea +K.Schum. (1904) + +407, syn. nov. — +Type +: +Braun s.n., anno 1888 +(holo +B +destroyed), +Cameroon +, +South Province +, +Gross-Batanga + +. + + + + +Costus bingervillensis +A.Chev. (1920) + +627, syn. nov. — +Type +: +Chevalier 15214 +(lecto +P +, designated here), +Ivory Coast +, +Bingerville region +, +Abidjan +, +Dabou +, + +19 Mar. 1905 + + +; + +other +syntypes +: +Chevalier 17280 +( +LY +, +P +p.p.), +Ivory Coast +, +Bingerville +, + +14–18 Dec. 1907 + +; the +specimen +in +P +is a mixed col-lection of + +C. afer + +and + +C. lucanusianus + +; +Chevalier 19883 +( +P +) + +, + +Ivory Coast +, +Tabou +, banks of +Bas-Cavally +, between +Prolo and Bliéron +, + +11 Aug. 1907 + + +. + + + +Fig. 3 + +Costus acutissimus +Maas & H.Maas. + +a. Habit showing distinct horizontal rims on base of shoot; b. bulbil in leaf axil; c. leaves with ligule; d. bract with 2 bracteoles and 2 calyces (a, b, d: +Van Valkenburg et al. 2768, +BR; c: +Thomas et al. 7938, +MO). — Drawing by Hendrik Rypkema. + + + + + +Costus insularis +A.Chev. (1920) + +627, nom. nud. Based on +Chevalier 13058 +( +P +), +Guinea +, +Iles de Los +, + +25 Feb. 1905 + + +. + + + + +Terrestrial herb, erect but in fruit sometimes individual shoots bending down, 0.5–4(–5) m tall. +Leaves +many; sheaths 0.8– 1(–1.5) cm diam; ligule chartaceous, 2-lobed to truncate, (2–) +4–11 mm +long, with a basal horizontal rim c. +1 mm +high, not completely encircling the shoot, sometimes bearing erect hairs to c. +3 mm +long; petiole +5–14 mm +long; sheaths, ligule and petiole glabrous to densely covered with erect to halfappressed white hairs < +1 mm +long; lamina narrowly elliptic to narrowly obovate, 7–25(–40) by (3–)4–10(–19) cm, upper side glabrous, lower side glabrous to rarely midrib densely covered with erect to half-appressed white hairs +1–2 mm +long, margin often with a row of hairs < +1 mm +long, base cordate to acute, apex acuminate (acumen +15–30 mm +long). +Inflorescence +many-flowered, globose to ellipsoid, (2.5–)4–14(–20) by 2.5–6(–8) cm, terminating the leafy shoot or rarely terminating a separate leafless shoot +10–30 cm +long; bracts, appendages of bracts, bracteoles and calyx glabrous, sometimes sparsely to rather densely covered with erect hairs < +1 mm +long, upper part of capsule densely covered with erect hairs < +1 mm +long. +Flowers +(1 or)2 per bract; bracts (pale) green often with reddish upper margin, coriaceous, ovate-triangular to depressed ovatetriangular, 2–3 by +2–2.5 cm +, callus +2–3 mm +long; appendages rarely present, green, horizontally spreading to reflexed, nar-rowly triangular, 4–10 by +2.5–3 cm +; bracteole boat-shaped, +14–25 mm +long, callus +1–4 mm +long; calyx 12–19(–22) mm long, lobes broadly ovate-triangular, (2–) +4–5 mm +long, erect and sometimes exceeding the bracts in fruit, callus +1–2 mm +long; corolla white to yellowish, +30–45 mm +long, glabrous, tube +5–10 mm +long, lobes (narrowly) elliptic, +20–40 mm +long; labellum at the outer side white, inner side white with (pale to dark) pink lateral marginal parts and yellow nectar guide, sometimes completely white with or without yellow nectar guide, funnel-shaped, broadly obovate when spread out, 30–45 by +35–50 mm +, margin crenulate; stamen white, 25–40 by +10 mm +, apex white, anther +6–9 mm +long. +Capsule +broadly obovoid, to 15(–20) mm diam. +Seeds +1–2 mm +diam. + + + + +Plate 1 +a. + +Costus afer +Ker Gawler. Flower. + +– b. + +Costus aureus +Maas & H.Maas. Inflorescence. + +– c. + +Costus albiflos +Maas & H.Maas. Inflorescence. + +– d. + +Costus dinklagei +K.Schum. Habit + +and details. – e. + +Paracostus englerianus +(K.Schum) C.D.Specht. Habit + +with flower. – f. + +Costus ligularis +Baker. Inflorescence + +(a: +Maas et al. 10023 +; b: photographed in Ghana,no specimen collected; c: +Maas et al. 10411 +; d: +N. Hallé 4129 +, drawing in his collecting book; e: photographed in Botanical gardens Utrecht, no specimen collected; f: +Maas et al. 9794 +). — Photos: a, c, f: P.J.M.Maas; b: T. +R.van Andel +; d: C.D.Specht; e: L.Y.T.Westra. + + + + +Map 3 +Distribution of + +Costus afer +Ker Gawl. + + + + +Distribution — North East Africa (Ethiopia, South Sudan); West Africa (Benin, Burkina Faso, Ghana, Guinea, GuineaBissau, Ivory Coast, Liberia, Nigeria, Senegal, Sierra Leone, Togo); Central Africa (Burundi, Cameroon, Central African Republic, Congo Brazzaville, Congo Kinshasa, Equatorial Guinea, Gabon, São Tomé & Principe); East Africa (Kenya, Tanzania, Uganda); Southern Tropical Africa (Angola, Malawi, Mozambique, Zambia, Zimbabwe). + + + +Habitat & Ecology — In open places like roadsides and forest margins, in secondary or savanna forest, often on wet places, near rivers; on sandy soil and on rocky outcrops, at elevations of +0–1770 m +. Flowering and fruiting: all year through. + + + +IUCN Conservation Status — Least Concern. + + + +Notes — + +Costus afer + +is characterized by an incomplete horizontal rim around the nodes of the shoot which is covered with only some erect hairs to c. +3 mm +long, a +4–11 mm +long ligule and erect calyx lobes that are sometimes exceeding the bracts in fruit. The corolla is white, the labellum is white with yellow nectar guide and reddish margins and the stamen is white with reddish apical part. + +Costus afer + +has often been confused with + +C. dubius + +, both species sharing green, unappendaged bracts and more or less white flowers, but + +C. afer + +is generally characterized by inflo-rescences terminating leafy shoots and flowers with a white labellum that has a yellow nectar guide and pink margins, while + +C. dubius + +generally has inflorescences on short, separate leafless shoots near the base of the plant and white flowers with a labellum bearing a yellow nectar guide but lacking pink margins. The bracts of + +C. afer + +are 1- or 2-flowered and sometimes appendaged, those of + +C. dubius + +are always 1-flowered and generally not appendaged. For the differences with + +C. lucanusianus + +, a species with which it has been sometimes confused, see under that species. For the differences with the similar looking + +C. louisii + +, see under that species. + + +The inflorescence of + +C. afer + +can terminate a leafy or leafless shoot as is known in many species of + +Costus + +; moreover, plants with 1- and/or 2-flowered bracts can be found all over the distribution area ( +Maas et al. 10023 +). The flower colour of + +C. afer + +is often (incorrectly) described on the collection label as ‘white’. This was the case in about 1/4 of the dried specimens included in this study. Indeed the corolla and the outer side of the labellum are white, but the inner side of the labellum is not completely white, but always has more or less reddish margins and a yellow nectar guide. The apical part of the stamen is white to pink. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB34FFFFFFCDFB9CFA89FBFE.xml b/data/38/76/87/387687E2BB34FFFFFFCDFB9CFA89FBFE.xml new file mode 100644 index 00000000000..829e82e26f5 --- /dev/null +++ b/data/38/76/87/387687E2BB34FFFFFFCDFB9CFA89FBFE.xml @@ -0,0 +1,260 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +6c0dbc52-820c-4f68-912d-1bcaa2227efc +7570023 + + + + + +1. + +Costus acutissimus +Maas & H.Maas + + +, + +sp. nov. +— + +Fig. 3 +; +Map 2 + + + + + +Costus acutissimus + +is characterized by narrow leaves with a long-acute apex (hence the specific name),a very short ligule ( +1–2 mm +long), a globose inflorescence ( +6–8 cm +diam) terminating a separate flowering shoot, green appendaged bracts and white flowers with yellow nectar guide. — + + + + + +Type +: +Van Valkenburg et al. 2768 +(holo WAG +3 +sheets [ +WAG0120332 +, +WAG0120333 +, +WAG0120334 +]; + + +iso +BR +, +LBV +[ +LBV0003152 +, +LBV0003153 +], +MO +, +P +), +Gabon +, +Nyanga +, +Moukalaba +, +Doudou National Park +, +Chantier +SFN-Bakker, + +250 m + +, + +16 Feb. 2004 + + +. + + + + +Terrestrial herb to c. +3 m +tall. +Leaves +many; sheaths +0.5–2 cm +diam, falling apart into separate fibers with age and leaving a distinct horizontal rim at the nodes near the base of the shoot; ligule chartaceous, 2-lobed, +1–2 mm +long; petiole +1–3 mm +long; sheaths, ligule and petiole glabrous to sparsely covered with minute appressed hairs < +1 mm +long and upper margin of ligule and sheaths with irregular curly fibers to c. +10 mm +long; lamina narrowly elliptic, 17–30 by +3.5–7 cm +, glabrous on both sides, base obtuse to cordate, apex long-acute to sometimes acuminate (acumen to c. +20 mm +long). +Inflorescence +manyflowered, globose, 6 – 8 by +6 –8 cm +, terminating a separate leafless shoot +10–30 cm +long; bracts, appendages of bracts, bracteoles, calyx, ovary and capsule sparsely covered with appressed hairs < +1 mm +long to glabrous; margin of bracts and calyx lobes densely covered with irregular curly fibers c. +1 mm +long. +Flowers +2 per bract; bracts pale green, chartaceous, broadly ovate-triangular, 2–4 by +2–3 cm +, callus absent; ap-pendages green, ascending, broadly ovate-triangular, 1– 2 by +1–2 cm +; bracteole boat-shaped, +20–25 mm +long, callus absent; calyx +25–28 mm +long, sometimes split to the base on one side, lobes narrowly triangular, +5–7 mm +long, callus absent; corolla white (not seen); labellum white, inner side with yellow nectar guide (not seen); stamen yellow (not seen). +Capsule +ellipsoid to obovoid, 10–17 by +7–10 mm +. +Seeds +c. 1.5 by +1–1.5 mm +. + + + +Distribution — Central Africa (Cameroon, Gabon). + + + +Habitat & Ecology — In moist valley bottom and on steep hill side. At elevations of + +250– +500 m. + +Flowering and fruiting: February, May. + + + + +IUCN Conservation Status — Based on an AOO of only +8 km + +2 +in + +two quite disjunct locations that both are part of National Parks, we assess this species as Vulnerable ( +VU +): D2. + + + + + +Other specimen examined. +CAMEROON +, + +South-West Province + +, S of Esukutang, +300–500 m +, +25 May 1988 +, +Thomas et al. 7938 +( +MO +) + +. + + + + +Note — Young shoots of + +C. acutissimus + +often show swollen nodes and small bulbils in the upper part of the shoot ( +Fig. 3b +). Old shoots have distinct horizontal rims of c. +1 mm +high, presumably remnants of withered sheaths ( +Fig. 3a +). + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB36FFFDFFCDFC12FA17FB34.xml b/data/38/76/87/387687E2BB36FFFDFFCDFC12FA17FB34.xml new file mode 100644 index 00000000000..8f61027bed1 --- /dev/null +++ b/data/38/76/87/387687E2BB36FFFDFFCDFC12FA17FB34.xml @@ -0,0 +1,159 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + + +Costaceae + + + + + + + +Costaceae +Nakai (1941) + +203. — +Type +: + +Costus + +L. + + + + +The African + +Costaceae + +( + +Costus +spp. + +and + +Paracostus englerianus + +) are perennial, rhizomatous herbs, terrestrial or epiphytic, rarely gigantic, tall (max. +6 m +), low or acaulescent herbs; shoot erect or prostrate, unbranched, generally spirally shaped, composed of nodes and internodes; leaf sheaths, petioles and lig-ules originating at the nodes. +Leaves +1, or few to many, spirally arranged along the shoot; shootless species with few leaves ro-sulate; prostrate species with 1 leaf per shoot ( + +Paracostus + +); leaf sheaths fully closed around the shoot; ligule present or rarely absent, membranous to chartaceous, tubular at the base and truncate to 2-lobed at the apex; petiole present or sometimes absent; lamina generally green, sometimes shiny, or plicate, herbaceous to coriaceous, generally elliptic with acuminate apex and acute base, sometimes extreme base of leaf fleshy surrounding the inflorescence ( + +Paracostus + +). +Inflorescence +a many-, several- or few-flowered spike, either terminating a leafy shoot, or terminating a separate leafless shoot, or lateral in the axil of a leaf, sometimes partially enclosed by the overlapping margins of the bases of the leaf lamina and the uppermost 1–3 sheathing leaf bases ( + +Paracostus + +); inflorescence ellipsoid to ovoid or globose when terminating a leafy shoot, loosely arranged when axillary; bracts spirally arranged, each carrying 1 or 2 flowers, yellow, green, red or brownish, membranous, chartaceous or coriaceous, generally ovate to triangular or elliptic, imbricate, callus linear, nectariferous, absent or present; foliaceous appendages absent or present, generally coloured as the bracts, ascending, horizontally spreading, or reflexed, broadly ovate to narrowly triangular; each flower enclosed by 1 bracteole, generally coloured as the bracts, boat-shaped or tubular and 1-keeled or sometimes 2-keeled, callus absent or 1 or 2 calli present. +Flowers +epigynous, bisexual, zygomorphic; calyx generally coloured as the bracts, tubular, 3-lobed or rarely 2-lobed, lobes erect, horizontally spreading, or reflexed, cal-lus absent or present; corolla white, yellow, orange, pink, lilac or reddish brown, or a combination of these colours, tubular, 3-lobed, lobes erect, narrowly obovate to elliptic, rarely hyaline; labellum large, longer than or as long as the corolla, white, yellow, orange, pink, lilac, dark red, reddish brown, purple, or a combination of these colours, sometimes with darker lateral parts and/or striped upper margin and central yellow nectar guide, horizontally flattened, funnel-shaped or rarely tubular, narrowly elliptic, ovate, obovate or subcylindrical when spread out, rarely lateral margins curved upwards ( + +C. giganteus + +), margin undulate to crenate, sometimes fimbriate; stamen 1, petaloid, generally yellow or white, apex recurved or erect and cucullate ( + +C. giganteus + +), anther longitudinally centred, composed of 2 narrowly elliptic 2-sporangiate thecae; base of stamen and labellum joined into a tube; gynoecium composed of a single ovary with attached style and stigma; ovary inferior, 3-locular, placentation axile, ovules many, organized in 2 rows per locule, anatropous; septal nectaries 2 at the apex of the ovary secreting nectar into the base of the floral tube; style 1, filamentous, supported between the thecae of the anther; stigma 1, 2-lamellate, hooked between the apices of the thecae by a dorsal 2-lobed to rounded appendage. In + +Paracostus englerianus + +the stigma is composed of a funnel-shaped upper part and a reflexed lamellate part, and the appendage is absent. +Fruit +capsular, 3-locular, placentation axile, generally obovoid, crowned by the persistent calyx, dehiscing loculicidally by three longitudinal slits, or indehiscent and irregularly breaking when old. +Seeds +numerous, black, shiny, irregularly angular reflecting tight packing in fruit; aril white, lacerate. + + + + + +KEY TO THE AFRICAN GENERA OF +COSTACEAE + + + +1. Plants erect, leaves generally more than two, occasion-ally in a basal rosette; inflorescence many-flowered, bracts conspicuous and often brightly coloured........ + +Costus + + + +1. Plants prostrate, leaves solitary, never in a basal rosette; inflorescence few-flowered, bracts inconspicuous and not brightly coloured....................... + +Paracostus + + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E2BB36FFFFFC84FB2FFD2EFBA9.xml b/data/38/76/87/387687E2BB36FFFFFC84FB2FFD2EFBA9.xml new file mode 100644 index 00000000000..73bca2a10c2 --- /dev/null +++ b/data/38/76/87/387687E2BB36FFFFFC84FB2FFD2EFBA9.xml @@ -0,0 +1,350 @@ + + + +Monograph of African Costaceae + + + +Author + +Kamer 1, H. Maas-van de + + + +Author + +Maas 1, P. J. M. + + + +Author + +Wieringa 1, J. J. + + + +Author + +Specht, C. D. + +text + + +Blumea + + +2016 + +2016-12-28 + + +61 + + +3 + + +280 +318 + + + + +http://dx.doi.org/10.3767/000651916x694445 + +journal article +10.3767/000651916X694445 +7570023 + + + + + + +Costus + + + + + + + +Costus + +L. (1753) 2. — +Type +: + +Costus arabicus +L. + + + + + +Perennial, rhizomatous herbs, terrestrial or epiphytic, rarely gigantic, tall, low or shootless herbs; shoot erect, unbranched, generally forming a spiral, composed entirely of sheathing leaf bases forming conspicuous nodes and internodes. +Leaves +few or many, spirally arranged along the shoot; shootless species with few leaves rosulate; leaf sheaths closed around the shoot; ligule present or rarely absent, membranous to chartaceous, tubular at the base and truncate to 2-lobed at the apex, sur-rounding the shoot above the proximal lobe as a continuation of the sheathing leaf base; petiole present or sometimes absent; lamina generally green, sometimes shiny, or plicate, herbaceous to coriaceous, generally elliptic with acuminate apex and acute base, upper side and lower side with various indument. +Inflorescence +a many-, several- or few-flowered spike, either terminating the leafy shoot, or terminating a separate leafless shoot, or lateral in the axil of a leaf, ellipsoid to ovoid or globose; bracts spirally arranged, each carrying 1 or 2 flowers, green, red or brownish, membranous, chartaceous or coriaceous, generally ovate to triangular or elliptic, imbricate, callus linear, nectariferous, absent or present; foliaceous appendages ab-sent or present, generally coloured as the bracts, ascending, horizontally spreading or reflexed, broadly ovate to narrowly triangular; each flower enclosed by 1 bracteole, generally col-oured as the bracts, boat-shaped or tubular and 1-keeled or sometimes 2-keeled, callus absent or 1 or 2 calli present. +Flowers +epigynous, perfect, zygomorphic; calyx generally coloured as the bracts, tubular at the base, 2(–3)-lobed, lobes erect, horizontally spreading, or reflexed, callus absent or present; corolla white, yellow, orange, pink, lilac or reddish brown, or a combination of these colours, tubular, 3-lobed, lobes erect, narrowly obovate to elliptic, rarely hyaline; labellum large, longer than or as long as the corolla, white, yellow, orange, pink, lilac, dark red, reddish brown, purple, or a combination of these colours, sometimes with darker lateral parts and/or striped margin and central yellow nectar guide, horizontally flattened, funnel-shaped, or rarely tubular, obovate to subcylindrical when spread out, margin undulate to crenate, sometimes fimbriate; stamen 1, petaloid, generally yellow or white, apex recurved, anther longitudinally placed in the middle, composed of two narrowly elliptic 2-sporangiate thecae; base of stamen and labellum joined into a tube; gynoecium composed of a single ovary, style and stigma; ovary inferior, 3-locular, placentation axile, ovules many, organized in 2 rows, anatropous, septal nectaries 2 at the base of the floral tube; style 1, terminal, cy-lindrical, filamentous, held between the thecae of the anther; stigma 1, 2-lamellate, hooked between the apices of the thecae by a dorsal 2-lobed to rounded appendage. +Fruit +capsular, 3-locular, generally obovoid, crowned by the persistent calyx, dehiscing loculicidally by three longitudinal slits or indehiscent and irregularly breaking when old. +Seeds +numerous, black, shiny, irregularly angular; aril white, lacerate. + + + +Distribution — Tropical to subtropical sub-Saharan Africa. + + + +Habitat & Ecology — Along with + +Marantaceae + +and + +Zingiberaceae + +, + +Costaceae + +form a significant part of the understory of the African tropical and subtropical rainforests. All three families +form part +of important herbaceous communities along forest margins, in forest gaps, and in the regrowth of disturbed forests (Dhetchuvi 1996). + + + + + +KEY TO THE AFRICAN SPECIES OF +COSTUS + + +1. Herbs acaulescent.............................. 2 +1. Herbs with shoots 0.5–6 m tall.................... 3 + +2. Calyx 35–75 mm long; anthers (6–)7–12(–15) mm long..................................19. + +C. macranthus + + + +2. Calyx 15–30 mm long; anthers 4–7(–12) mm long...................................... 22. + +C. spectabilis + + +3. Epiphytic plants with inflorescences lateral in the axil of a leaf, or terminating a leafy or leafless shoot.......... 4 +3. Terrestrial plants with inflorescences terminating a leafy or leafless shoot................................. 6 +4. Bracts 1-flowered; flowers yellow or pale lilac with yellow nectar guide................................... 5 + +4. Bracts 2-flowered; flowers white to dark pink with yellow nectar guide......................... 23. + +C. talbotii + + + +5. Flowers completely yellow........... 12. + +C. lateriflorus + + + +5. Flowers pale lilac with yellow nectar guide 14. + +C. lilaceus + + +6. Inflorescence generally terminating a separate leafless shoot, emerging directly from the rhizome............ 7 +6. Inflorescence generally terminating a leafy shoot..... 18 + +7. All bracts provided with appendages ( +Fig. 1e +)......... 8 + +7. Bracts generally without appendages (often the lowermost bracts appendaged but all the other ones not)....... 11 +8. Flowers white with yellow nectar guide.............. 9 +8. Flowers differently coloured...................... 10 + +9. Ligule 1–2 mm long; petiole 1–3 mm long; flowers 2 per bract, appendages ascending; inflorescence globose (6–8 by 6–8 cm) on a separate leafless shoot 10–30 cm long................................. 1. + +C. acutissimus + + + +9. Ligule 10–30 mm long; petiole 5–10 mm long; flower 1 per bract, appendages horizontally spreading; inflorescence ovoid (4–12 by 3–8 cm) on a separate leafless shoot 10–50 cm long............................. 3. + +C. albiflos + + + +10. Flowers with white to purplish grey or reddish brown label- lum; plant glabrous; bracts green; bracteole with an incon-spicuous callus; leaf sheaths green with reddish margin; apex of leaves acuminate (acumen15–40 mm long)............................... 18. + +C. maboumiensis + + + +10. Flowers with white labellum with pink to purple margin; upper and lower side of leaves densely covered with soft erect hairs to c. 3 mm long; bracts dark brown-red; brac-teole with a distinct callus; leaf sheaths dark red; apex of leaves acute to acuminate (acumen c. 10 mm long)..................................... 13. + +C. ligularis + + +11. Bracts green................................ 12 +11. Bracts red to brown........................... 15 +12. Sheaths, ligule, petiole and leaves glabrous........ 13 +12. Sheaths, ligule, petiole and leaves very densely covered with brown hairs 0.5–2 mm long................. 14 + +13. Flowers white to purplish grey or reddish brown................................... 18. + +C. maboumiensis + + + +13. Flowers white with yellow nectar guide.... 6. + +C. dubius + + + +14. Corolla lobes salmon-coloured; labellum white with 2 dark pink patches at the base and a yellow nectar guide, horizontally flattened..................... 20. + +C. nimba + + + +14. Corolla lobes whitish; labellum white to pale pink with yel-low nectar guide, funnel-shaped........ 5. + +C. dinklagei + + +15. Bracts brown to reddish brown, 1- or 2-flowered; labellum not tubular; separate leafless shoot 1–9 cm long.... 16 + +15. Bracts red, 1-flowered; labellum tubular; separate leafless shoot 100–150 cm long.............. 9. + +C. giganteus + + +16. Bracts 2-flowered; flowers white to dark pink with yellow nectar guide................................. 17 + +16. Bracts 1-flowered; flowers completely yellow.......................................... 11. + +C. kupensis + + + +17. Labellum white to dark pink with yellow nectar guide; ligule 40–55 mm long; leaves not bullate nor plicate, base obtuse to acute........................... 23. + +C. talbotii + + + +17. Labellum dark pink to white with yellow nectar guide; lig-ule 1–5 mm long; leaves bullate and 5–10-plicate, base cordate................... 24. + +C. tappenbeckianus + + +18. All bracts provided with appendages.............. 19 +18. Bracts generally without appendages (often the lowermost bracts appendaged but all the other ones not)...... 23 +19. Flowers completely yellow..................... 20 +19. Flowers differently coloured.................... 21 + +20. Ligule 1–5 mm long; appendages of bracts green, ascend-ing; flowers not aromatic............... 4. + +C. aureus + + + +20. Ligule 5–35 mm long; appendages of bracts pinkish red to purplish brown, strongly reflexed; flowers strongly aro-matic.......................... 8. + +C. gabonensis + + + +21. Bracts soon falling apart into separate fibers ( +Fig. 4c +), leaves obovate, 4, c. 20-plicate; petiole 0–3 mm long.................................. 7. + +C. fenestralis + + +21. Bracts not falling apart into separate fibers, leaves not obovate, not plicate, generally more than 4; petiole 3–15 mm long................................... 22 + +22. Bracts apically dark brown-red; labellum white with pink to purple, without nectar guide; callus on bracteole distinct, 1.5–2 mm long; inflorescence few- to several-flowered, 1–4 by 1–4 cm; upper side of leaves covered with soft erect hairs to c. 3 mm long............ 13. + +C. ligularis + + + +22. Bracts green to reddish purple; labellum pink to dark pink or white, with yellow nectar guide; callus on bracteole present, 2–3.5 mm long ( +Fig. 1e +); inflorescence manyflowered, 2.5–10 by 3–7 cm; upper side of leaves generally glabrous.................... 21. + +C. phyllocephalus + + +23. Bracts red to reddish brown.............. ... ... 24 23. Bracts completely green................. ... ... 26 24. Labellum horizontally flattened, either completely yellow or dark pink; leaf sheaths 6–11 mm diam; calyx 11–20 mm long................................. .. .... 25 + +24. Labellum tubular; flowers red or yellow to orange; leaf sheaths 2–6 mm diam; calyx 7–10 mm long........................................ 10. +C. + +gracillimus + +25. Herbs 1.5–2.5 m tall; leaves distinctly shiny, glabrous; calyx 17–20 mm long; flowers white and pink... 16. + +C. louisii + + + +25. Herbs to 0.6 m tall; leaves not shiny, densely covered with erect to half-appressed hairs 1.5–2 mm long on both sides; calyx 11–12 mm long; flowers completely yellow..................................... 15. +C. + +loangensis + + +26. Corolla lobes not hyaline, white; labellum white with yel-low and pink or red; ligule 1–11 mm long, with distinct rim around its base.............................. 27 + + +Map 2 +Distribution of + +Costus acutissimus +Maas & H.Maas + +(▲), + +C. albiflos +Maas & H.Maas + +(●) and + +C. aureus +Maas & H.Maas + +(■). + + + +26. Corolla lobes hyaline, salmon-coloured; labellum white with salmon and 2 dark pink zones at the base; ligule 14–23 mm long without a distinct rim........... 20. + +C. nimba + + + +27. Flowers white with yellow and pink; calyx in fruit about as long as the bracts, lobes erect; ligule 4–11 mm long, generally with a glabrous incomplete rim around its base; leaves glabrous........................ 2. + +C. afer + + + +27. Flowers white with yellow, orange and dark red; calyx in fruit exceeding the bracts, lobes horizontally spreading to reflexed; ligule 1–4 mm long, with a complete hairy rim around its base; lower side of leaves often silvery (covered with mainly erect hairs to c. 2 mm long).......................................... 17. + +C. lucanusianus + + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E3FA00FFDBFF7289CA9D78965E.xml b/data/38/76/87/387687E3FA00FFDBFF7289CA9D78965E.xml new file mode 100644 index 00000000000..d950427a946 --- /dev/null +++ b/data/38/76/87/387687E3FA00FFDBFF7289CA9D78965E.xml @@ -0,0 +1,128 @@ + + + +Five new leafhopper species of the genus Typhlocyba Germar (Hemiptera: Cicadellidae: Typhlocybinae) from China + + + +Author + +Huang, Min + + + +Author + +Zhang, Ya-Lin + +text + + +Zootaxa + + +2009 + +1972 + + +44 +52 + + + +journal article +10.5281/zenodo.185061 +5445131e-0949-4b9a-a181-fd46c5757b57 +1175-5326 +185061 + + + + + + + +Typhlocyba serrata + +sp. nov. + + + + +Figs 32–42 +. + + + + +Description. +Color pattern of dorsum as in +Fig. 32 +. Vertex with elliptical patch at most anterior margin extending to face and patches next to eyes, yellowish-orange, short streaks near to lateral margin brown; pronotum and scutellum with reddish-orange patches at anterior and posterior margin, yellowish-orange at central pronotum; forewing with basal patches yellowish-orange, with central patches yellowish-ocher, and with all patches bordered with brown; brochosome field with basal end yellowish-orange, distal end yellowishocher; apical part of forewing infuscate, apical veins yellowish. Dorsal part of abdomen, pygofer capsule and anal tube dark brown. + +Abdominal apodemes reaching to end of 5th abdominal sternite. + +Male genitalia: Pygofer side broad with several teeth at upper angle of posterior margin and below with some short and rigid microsetae ( +Figs 35–36 +). Subgenital plate with distal 1/3 narrowed and twisted ventrolaterally ( +Figs 37–38 +). Paramere with caudal part slim and tapering more than twice length of central part ( +Fig. 39 +). Connective nearly M-shaped ( +Fig. 37 +). Aedeagal shaft relatively straight with pair of parallel distal processes, serrated on outer margin and directed ventrobasally ( +Figs 40–42 +). + + +Measurement: +male, 2.57 mm (including wings). + + + + + +Type +material. + +Holotype +: ɗ, +CHINA +. Yunnan Province: Sanchahe, +7.vi.1991 +, coll. Rungang Tian; ( +NWAFU +); +paratypes +, 16ɗ, same data as +holotype +( +NWAFU +and including +2 in +BMNH +) + + +Notes. +The new species belongs to the + +T. arborea + +group and resembles + +T. yacaba +Dworakowska (1994) + +in colour pattern and male genitalia but can be distinguished by aedeagus with processes apically and directed ventrobasally and with serrations at outer margin. + + + + +Etymology. +The specific name is derived from Latin word serratus, meaning jagged like a saw referring to the serrated processes of aedeagus. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E3FA01FFDBFF72885A9B639260.xml b/data/38/76/87/387687E3FA01FFDBFF72885A9B639260.xml new file mode 100644 index 00000000000..61e2ff66c85 --- /dev/null +++ b/data/38/76/87/387687E3FA01FFDBFF72885A9B639260.xml @@ -0,0 +1,145 @@ + + + +Five new leafhopper species of the genus Typhlocyba Germar (Hemiptera: Cicadellidae: Typhlocybinae) from China + + + +Author + +Huang, Min + + + +Author + +Zhang, Ya-Lin + +text + + +Zootaxa + + +2009 + +1972 + + +44 +52 + + + +journal article +10.5281/zenodo.185061 +5445131e-0949-4b9a-a181-fd46c5757b57 +1175-5326 +185061 + + + + + + + +Typhlocyba triannulata + +sp. nov. + + + + +Figs 23–31 +. + + + + +Description. +Color pattern of dorsum as in +Fig.23 +. Patches on vertex orange or light orange, on pronotum and scutellum orange. Forewing with distal part of lognitudinal veins and transverse and apical veins yellowish, with basal patches yellowish ocher or yellowish orange; patches on both ends of brochosome field brown, apical part infuscate; subgenital plate and end of anal tube, ivory, remainder of abdomen including pygofer capsule, dark brown. + + + +FIGURES 23–31. + +Typhlocyba triannulata + + +sp. nov. + +23, Habitus, dorsal view. 24, Abdominal apodemes. 25, Male pygofer, lateral view. 26, Posterior part of male pygofer, lateral view. 27, Paramere, connective, subgenital plate and sternite IX, dorsal view. 28, Apical part of subgenital plate. 29, Paramere. 30, Aedeagus, posterior view. 31, Aedeagus, lateral view. + + +Abdominal apodemes reaching to base of 5th abdominal sternite. + +Male genitalia: Pygofer side narrowing caudally ( +Fig. 25 +), with well developed broad finger-like protrusion at upper angle of posterior margin, with 2–3 teeth at caudoventral margin, margin between protrusion and teeth with some rigid microsetae ( +Fig. 26 +). Subgenital plate slender with 2 groups of rigid microsetae at inner and outer apical margin, apex hook-like ( +Fig. 28 +). Paramere pigmented with distal part slender ( +Fig. 29 +). Connective well developed, stem slender, nearly twice length of arms ( +Fig.27 +). Aedeagal shaft relatively short with pair of bifurcate, distally directed, subapical processes ( +Figs 30–31 +). + + +Measurement: +male, 3.63 mm (including wings). + + + + + +Type +material. + +Holotype +: ɗ, +CHINA +. Sichuan Province: Mianning, Alt. +1650 m +, +8.xi.1999 +, coll. I. Dworakowska; +paratype +, 1ɗ, Sichuan Province: Batang, Zhubalong, Alt. +2450 m +, +10.vii.2001 +, coll. Qiang Sun, light trap (both +NWAFU +). + + +Notes. +The new species belongs to + +T. arborea + +group and is similar to + +T. equata +Dworakowska (1982) + +in color pattern, but can be distinguished from the latter by 1) pygofer side with long protrusion at upper angle of posterior margin; 2) subgenital plate with apex hook-like; 3) connective nearly Y-shaped; 4) aedeagal subapical processes bifurcate; while in + +T. equata + +pygofer side with protrusion not obvious; subgenital plate with apex finger-like; connective nearly M-shaped; aedeagal processes not furcated. + + + + +Etymology. +The specific name is a combination of the Latin prefix tri- meaning three and the Latin word annulus, meaning ring, referring to the three ring-like marks on the forewings. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E3FA03FFD6FF728CD69C8A91E0.xml b/data/38/76/87/387687E3FA03FFD6FF728CD69C8A91E0.xml new file mode 100644 index 00000000000..b1c8715c6ea --- /dev/null +++ b/data/38/76/87/387687E3FA03FFD6FF728CD69C8A91E0.xml @@ -0,0 +1,142 @@ + + + +Five new leafhopper species of the genus Typhlocyba Germar (Hemiptera: Cicadellidae: Typhlocybinae) from China + + + +Author + +Huang, Min + + + +Author + +Zhang, Ya-Lin + +text + + +Zootaxa + + +2009 + +1972 + + +44 +52 + + + +journal article +10.5281/zenodo.185061 +5445131e-0949-4b9a-a181-fd46c5757b57 +1175-5326 +185061 + + + + + + + +Typhlocyba bilaminata + +sp. nov. + + + + +Figs 43–52 +. + + + + +Description. +Color pattern of dorsum as in +Fig. 43 +. Patches on vertex and pronotum orange, basal triangles of scutellum reddish brown surrounded by reddish orange, end of scutellum and basal patches of forewing, reddish orange; distal end of brochosome field brownish orange with apical part infuscate. Abdomen with dorsal part brown, pygofer with upper posterior part dark brown, end of anal tube light orange. + +Abdominal apodemes reaching to end of 5th abdominal sternite. + + +FIGURES 43–52. + +Typhlocyba bilaminata + + +sp. nov. + +43, Habitus, dorsal view. 44, Abdominal apodemes. 45, Male pygofer, lateral view. 46, Posterior part of male pygofer, lateral view. 47, Paramere, connective, subgenital plate and sternite IX, dorsal view. 48, Apical part of subgenital plate. 49, Paramere. 50, Connective. 51, Apical part of aedeagal shaft, dorsal view. 52, Aedeagus, lateral view. + + + +Male genitalia: Pygofer side bilobed at posterior margin, upper lobe triangular and pigmented, lower one truncate and with several rigid microsetae along posterior margin ( +Figs 45–46 +). Subgenital plate broadened basally, narrowed medially, and slightly broadened again distally ( +Fig. 47 +), with hook-like protrusion subapically ( +Fig. 48 +). Paramere with central part robust ( +Fig. 49 +). Connective robust, nearly M-shaped ( +Fig. 50 +). Aedeagal shaft moderately slender and angularly curved, with pair of long parallel distal processes, bladelike, directed dorsally ( +Figs 51–52 +). + + +Measurement: +male, 3.05 mm (including wings). + + + + + +Type +material. + +Holotype +: ɗ, +CHINA +. Yunnan Province: Sanchahe, +7.vi.1991 +, coll. Rungang Tian ( +NWAFU +); +paratypes +, 22ɗ, same data as +holotype +( +NWAFU +and including +2 in +BMNH +). + + +Notes. +The new species belongs to + +T. aptera + +group and is similar to + +T. aptera +Dworakowska (1979) + +in male genitalia but can be distinguished from the latter by paired blade-like distal processes of aedeagal shaft. + + + + +Etymology. +The specific name is a combination of the Latin prefix bi meaning two and the Latin word lamina, meaning blade which refers to blade-like aedeagal processes. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E3FA04FFDCFF728F179B4B9068.xml b/data/38/76/87/387687E3FA04FFDCFF728F179B4B9068.xml new file mode 100644 index 00000000000..fabec5275cc --- /dev/null +++ b/data/38/76/87/387687E3FA04FFDCFF728F179B4B9068.xml @@ -0,0 +1,143 @@ + + + +Five new leafhopper species of the genus Typhlocyba Germar (Hemiptera: Cicadellidae: Typhlocybinae) from China + + + +Author + +Huang, Min + + + +Author + +Zhang, Ya-Lin + +text + + +Zootaxa + + +2009 + +1972 + + +44 +52 + + + +journal article +10.5281/zenodo.185061 +5445131e-0949-4b9a-a181-fd46c5757b57 +1175-5326 +185061 + + + + + + + +Typhlocyba napoensis + +sp. nov. + + + + +Figs 1–11 +. + + + + +Description. +Color pattern of dorsum as in +Figs 1–2 +. Patches on pronotum and scutellum and irregularly sinuated band on forewing, reddish-orange; basal triangles of scutellum surrounded by red streaks; small spot on base of 3rd apical cell blackish brown. Abdomen ivory. + +Abdominal apodemes reaching to end of 5th abdominal sternite. + +Male genitalia: Pygofer side tapering, with short finger-like protrusion at upper angle of posterior margin, with few setae beneath ( +Figs 4–5 +). Subgenital plate slender gradually narrowing caudad and knob-like terminally ( +Fig. 6 +); several short setae apically and subapically ( +Fig. 7 +). Paramere slim ( +Fig. 8 +). Connective nearly M –shaped ( +Fig. 9 +). Aedeagal shaft arcuate, with pair of basal processes sculptured on apical 1/3, sinuate and exceeding end of shaft ( +Figs 10–11 +). + + +Measurement: +Male, 2.94 mm (including wings). + + + + + +Type +material. + +Holotype +: ɗ, +CHINA +. Guangxi Province: +Napo, Defu +, +19.vi.2000 +, coll. Chaodong Zhu; +paratype +, 1ɗ, +19.vi.2000 +, same date as +holotype +, coll. Jian Yao (both +IZAS +). + + +Notes. +The new species belongs to + +T. quercus + +group and resembles + +T. irenae +Sharma (1984) + +in male genitalia, but can be distinguished by 1) aedeagal shaft with basal processes longer, exceeding end of shaft, while in + +T. irenae + +processes not reaching apex of shaft; 2) aedeagal shaft processes sinuate and close to shaft in posterior view, rather than straight and detached from shaft as in + +T. irenae + +; 3) color pattern on forewing brighter and uninterrupted, while in + +T. irenae + +patches on forewing irregular and interrupted. + + + + +Etymology. +The specific name is derived from the +type +locality, Napo. + + + + \ No newline at end of file diff --git a/data/38/76/87/387687E3FA05FFDFFF728CC09E139068.xml b/data/38/76/87/387687E3FA05FFDFFF728CC09E139068.xml new file mode 100644 index 00000000000..fa149d98d63 --- /dev/null +++ b/data/38/76/87/387687E3FA05FFDFFF728CC09E139068.xml @@ -0,0 +1,94 @@ + + + +Five new leafhopper species of the genus Typhlocyba Germar (Hemiptera: Cicadellidae: Typhlocybinae) from China + + + +Author + +Huang, Min + + + +Author + +Zhang, Ya-Lin + +text + + +Zootaxa + + +2009 + +1972 + + +44 +52 + + + +journal article +10.5281/zenodo.185061 +5445131e-0949-4b9a-a181-fd46c5757b57 +1175-5326 +185061 + + + + + + + +Typhlocyba +Germar, 1833 + + + + + + + + + +Typhlocyba +Germar, 1833: 180 + +; Anufriev 1973: 505; + +Dworakowska 1979 +: 195 + +. + +Anomia +Fieber 1866a: 509 + +. + + + + + + +Type +species: + + +Cicada quercus +Fabricius. + + + + + +Diagnosis. +Body slim and usually brightly colored, orange, yellowish-orange or reddish-orange. Head produced medially, median length usually longer than width between eyes. Forewing with 3rd apical cell triangular, petiolate. Hindwing with 2 open apical cells. + +Abdominal apodemes not exceeding 6th sternite. Subgenital plate with single long macroseta near outer basal angle, apex often modified. Paramere slender, without apical tooth. Connective short and robust, nearly M- or Y-shaped. Aedeagus with shaft slim; processes derived from base or apex of shaft, paired or single; gonopore apical. + + + \ No newline at end of file diff --git a/data/38/76/87/387687E3FA07FFDAFF728D5E9DED90F0.xml b/data/38/76/87/387687E3FA07FFDAFF728D5E9DED90F0.xml new file mode 100644 index 00000000000..3c7bd2cac57 --- /dev/null +++ b/data/38/76/87/387687E3FA07FFDAFF728D5E9DED90F0.xml @@ -0,0 +1,144 @@ + + + +Five new leafhopper species of the genus Typhlocyba Germar (Hemiptera: Cicadellidae: Typhlocybinae) from China + + + +Author + +Huang, Min + + + +Author + +Zhang, Ya-Lin + +text + + +Zootaxa + + +2009 + +1972 + + +44 +52 + + + +journal article +10.5281/zenodo.185061 +5445131e-0949-4b9a-a181-fd46c5757b57 +1175-5326 +185061 + + + + + + + +Typhlocyba tubercula + +sp. nov. + + + + +Figs 12–22 +. + + + + +Description. +Color pattern of dorsum as in +Figs 12–14 +. Patches on vertex yellowish, thin streak on the lateral margin of vertex entending to anterior margin of face, then joining streak on anterolateral margin of face, brown; clypeus and gena dark brown. Patches on anterior and lateral part of pronotum and on basal half of forewing reddish-orange, on the pronotum centrally orange, on distal end of clavus and adjacent area of corium yellowish-orange and on distal end of brochosome field dark brown; apical part of forewing infuscate. Abdomen and genital capsule dark brown. + + +Vertex concave centrally, with anterior margin produced apically, longer than pronotum ( +Figs 12–13 +). + +Abdominal apodemes reaching to end of 5th abdominal sternite. + +Male genitalia: Pygofer side with long finger-like protrusion at upper angle of posterior margin, serrated ventrally ( +Fig. 16 +). Subgenital plate broad basally, abruptly narrowed at median with apex digitate and twisted laterally ( +Fig. 17 +); corner of apex with a big tuberculate-like protrusion bearing numerous rigid microsetae ( +Fig. 18 +). Paramere slim and with base pigmented (Figs 17,19). Connective pigmented, nearly M –shaped ( +Fig. 20 +). Aedeagal shaft slim with pair of subapical upturned processes, broadened basally ( +Figs 21–22 +). + + + +FIGURES 12–22. + +Typhlocyba tubercula + + +sp. nov. + +12, Habitus, dorsal view. 13, Anterior dorsum (crown, pronotum and scutellum, lateral view). 14, Face. 15, Abdominal apodemes. 16, Male pygofer, lateral view. 17, Paramere, connective, subgenital plate and sternite IX, dorsal view. 18, Apical part of subgenital plate. 19, Paramere. 20, Connective. 21, Aedeagus, posterior view. 22, Aedeagus, lateral view. + + + +Measurement: +male, 3.39 mm (including wings). + + + + + +Type +material. + +Holotype +: ɗ, +CHINA +. Yunnan Province: Sanchahe, +7.vi.1991 +, coll. Rungang Tian; +paratype +, 1ɗ, same data as +holotype +(both +NWAFU +). + + +Notes. +The new species belongs to + +T. arborea + +group and comes close to + +T. equata +Dworakowska (1982) + +in shape of aedeagus but characteristics of pygofer, paramere and connective are similar to + +T. quercus + +group. The most characteristic features of the new species are apically produced and centrally concave vertex and shape of the subgenital plate which becomes abruptly slender at mdlength and bears a big tuberculate protrusion at its apex. + + + + +Etymology. +The specific name is derived from Latin word tuber, meaning protuberance, which refers to subgenital plate with a protrusion at its apex. + + + + \ No newline at end of file diff --git a/data/38/76/92/3876923A49A7B4A40488CCD2357F2B08.xml b/data/38/76/92/3876923A49A7B4A40488CCD2357F2B08.xml new file mode 100644 index 00000000000..457162a8035 --- /dev/null +++ b/data/38/76/92/3876923A49A7B4A40488CCD2357F2B08.xml @@ -0,0 +1,225 @@ + + + +New records and detailed distribution and abundance of selected arthropod species collected between 1999 and 2011 in Azorean native forests + + + +Author + +Borges, Paulo A. V. + + + +Author + +Gaspar, Clara + + + +Author + +Crespo, Luis Carlos Fonseca + + + +Author + +Rigal, Francois + + + +Author + +Cardoso, Pedro + + + +Author + +Pereira, Fernando + + + +Author + +Rego, Carla + + + +Author + +Amorim, Isabel R. + + + +Author + +Melo, Catarina + + + +Author + +Aguiar, Carlos + + + +Author + +Andre, Genage + + + +Author + +Mendonca, Enesima P. + + + +Author + +Ribeiro, Servio + + + +Author + +Hortal, Joaquin + + + +Author + +Santos, Ana M. C. + + + +Author + +Barcelos, Luis + + + +Author + +Enghoff, Henrik + + + +Author + +Mahnert, Volker + + + +Author + +Pita, Margarida T. + + + +Author + +Ribes, Jordi + + + +Author + +Baz, Arturo + + + +Author + +Sousa, Antonio B. + + + +Author + +Vieira, Virgilio + + + +Author + +Wunderlich, Joerg + + + +Author + +Parmakelis, Aristeidis + + + +Author + +Whittaker, Robert J. + + + +Author + +Quartau, Jose Alberto + + + +Author + +Serrano, Artur R. M. + + + +Author + +Triantis, Kostas A. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +10948 +10948 + + + + +http://dx.doi.org/10.3897/BDJ.4.e10948 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e10948 +1314-2828--10948 + + + + +Thrips atratus Haliday, 1836 + + + +Ecological interactions + +Native status +Native + + + +Distribution +FAI; PIC; SJG; TER; SMG; SMR + + +Notes +Also present: MAD (Biogeographical Realm: Holarctic) + + + \ No newline at end of file diff --git a/data/38/76/9D/38769D1BFFB2FF971BCCFBCB20A0D7A5.xml b/data/38/76/9D/38769D1BFFB2FF971BCCFBCB20A0D7A5.xml new file mode 100644 index 00000000000..680feb3ba8b --- /dev/null +++ b/data/38/76/9D/38769D1BFFB2FF971BCCFBCB20A0D7A5.xml @@ -0,0 +1,211 @@ + + + +Two new species of Manulea Wallengren, 1863 from southwestern China and northern Vietnam (Lepidoptera: Erebidae: Arctiinae: Lithosiini) + + + +Author + +Volynkin, Anton V. +0000-0001-9447-4925 +Altai State University, Lenina Avenue, 61, RF- 656049, Barnaul, Russia & monstruncusarctia @ gmail. com; https: // orcid. org / 0000 - 0001 - 9447 - 4925 +monstruncusarctia@gmail.com + + + +Author + +Saldaitis, Aidas +0000-0003-0999-3996 +Nature Research Centre, Akademijos str., 2, LT- 08412, Vilnius- 21, Lithuania & saldrasa @ gmail. com; https: // orcid. org / 0000 - 0003 - 0999 - 3996 +saldrasa@gmail.com + +text + + +Zootaxa + + +2021 + +2021-06-24 + + +4991 + + +2 + + +389 +397 + + + +journal article +5538 +10.11646/zootaxa.4991.2.12 +da3a8e32-ba5c-4043-90c3-909cd8ceff35 +1175-5326 +5030434 +DA474873-9729-4F7A-9CEE-875F9397F1BD + + + + + + + +Manulea postmaculosa +( +Matsumura, 1927 +) + +, +stat. rev. +& comb. nov. + + + + + + +( +Figs 9–15 +, +20, 21 +, +26 +) + + + + + +Lithosia postmaculosa + +Matsumura, 1927 + + +, + +Journal of the +College of Agriculture +, Hokkaido Imperial University + +, +19 +(1): 66, pl. 5, fig. 9 ( +Type +locality: [ +Taiwan +, +Nantou County +, +Meiyuan +] +Formosa +, +Baibara +). + + + + +Type material examined +. + +Photograph of the + +holotype + +( +Fig. 12 +): female, “Baibara, +Y +. Saito Kikuchi” / “ + +Lithosia postmaculosa + +” / red label “Type Matsumura” ( +EIHU +) + +. + + +Other material examined +: long series of both sexes from +Taoyuan +, +Pingtung +, +Taichung +, +Kaohsiung +, +Nantou +, Ilan, +Chiayi +and +Taipei +Counties of +Taiwan +, gen. slide Nos.: +ZSM +Arct. 2020-160, +ZSM +Arct. 2020-162, +ZSM +Arct. 2020-164 (males), +ZSM +Arct. 2020-161, +ZSM +Arct. 2020-163, +ZSM +Arct. 2020-165 (females) (prepared by Volynkin) ( +MWM +/ +ZSM +). + + + + +Diagnosis +. The forewing length is +15–16 mm +in males and 15.5– +16 mm +in females. The species is variable in its wing coloration. However, the male and the female genitalia of different forms display no remarkable differences. The differences between + +M. postmaculosa + +and + +M. lienquan + +are discussed in details above in the diagnosis of the latter species. + + + + +Distribution +. The species is endemic to +Taiwan Island +( +Fang, 1982 +; +2000 +partim; Chang 1989; +Heppner 2012 +, as + +costipuncta postmaculosa + +). + + + + \ No newline at end of file diff --git a/data/38/76/9D/38769D1BFFB2FF9B1BCCF88E221FD18B.xml b/data/38/76/9D/38769D1BFFB2FF9B1BCCF88E221FD18B.xml new file mode 100644 index 00000000000..dabbc87cc93 --- /dev/null +++ b/data/38/76/9D/38769D1BFFB2FF9B1BCCF88E221FD18B.xml @@ -0,0 +1,236 @@ + + + +Two new species of Manulea Wallengren, 1863 from southwestern China and northern Vietnam (Lepidoptera: Erebidae: Arctiinae: Lithosiini) + + + +Author + +Volynkin, Anton V. +0000-0001-9447-4925 +Altai State University, Lenina Avenue, 61, RF- 656049, Barnaul, Russia & monstruncusarctia @ gmail. com; https: // orcid. org / 0000 - 0001 - 9447 - 4925 +monstruncusarctia@gmail.com + + + +Author + +Saldaitis, Aidas +0000-0003-0999-3996 +Nature Research Centre, Akademijos str., 2, LT- 08412, Vilnius- 21, Lithuania & saldrasa @ gmail. com; https: // orcid. org / 0000 - 0003 - 0999 - 3996 +saldrasa@gmail.com + +text + + +Zootaxa + + +2021 + +2021-06-24 + + +4991 + + +2 + + +389 +397 + + + +journal article +5538 +10.11646/zootaxa.4991.2.12 +da3a8e32-ba5c-4043-90c3-909cd8ceff35 +1175-5326 +5030434 +DA474873-9729-4F7A-9CEE-875F9397F1BD + + + + + + + +Manulea labahe + +sp. nov. + + + + + + +( +Figs 7, 8 +, +22 +) + + + + +Type material +. + + +Holotype + +( +Figs 7 +, +22 +): male, “ +China +, +W +. +Sichuan +, road +Ya’an +/ +Kangding +, near Labahe Nac. park, + +20.IV.2010 + +, leg. +Chen Gun +”, gen. slide +No. +: +AV6414 +(prepared by +Volynkin +) ( +AFM +). + + + + + +Paratype + +: +1 male +, the same data as in the +holotype +, gen. slide No.: +AV6413 +(prepared by Volynkin) + +( +AFM +). + + + + +FIGURES 17–19 +. + +Manulea +spp. + +: male genitalia. Depositories of the specimens: 17 in MWM/ZSM; 18 and 19 in AFM. + + + + +FIGURES 20–23 +. + +Manulea +spp. + +: male genitalia. Depositories of the specimens: 20, 21 and 23 in MWM/ZSM; 22 in AFM. + + + + +Diagnosis +. The male of + +M. labahe + +is reminiscent superficially of the + +M. postmaculosa + +/ + +M. lienquan + +species pair due to its forewing colouration and the forewing shape. However, it can easily be distinguished by the lack of black medial spots (present in the congeners) and the presence of two sinuous greyish brown transverse lines (absent in the congeners). The male genital capsule of + +M. labahe + +differs from those of the congeners by the uncus strongly dilated distally, the vesica having small apico-lateral processes (absent in the congeners), the less convex costal margin of the valva, and the narrower sacculus lacking a dentate tubercle-like process at the base of the distal saccular process (present in the congeners). Additionally, the arms of the vinculum of the new species are distally connected by a membranous commissure, whereas in the congeners the commissure is sclerotized. Compared to those of the congeners, the aedeagus of the new species is markedly narrower, and the vesica is much narrower and lacking a large distal diverticulum with apical sclerotization. The cornutus of + +M. labahe + +is nearly straight, uniformly narrow and pointed apically, whereas in the + +M. postmaculosa + +/ + +M. lienquan + +species pair it is robust, broad basally, curved medially and arrowhead-like dilated apically. + + + + +FIGURES 24–26 +. + +Manulea +spp. + +: female genitalia. Depositories of the specimens: 24 and 26 in MWM/ZSM; 25 in AFM. + + + + +Description +. +External morphology of adults +( +Figs 7, 8 +). Forewing length +18–19 mm +in males. Male antenna ciliate. Body brown, abdomen with admixture of ochreous hair-like apically. Forewing elongate with strongly convex costal margin and elongate apex. Forewing ground colour brown.Antemedial and postmedial transverse line greyish brown, sinuous, diffuse. Cilia brown with admixture of greyish scales. Hindwing monotonous pale ochreous. +Male genitalia +( +Fig. 22 +). Uncus elongate, strongly dilated distally, with convex dorsal margin and tiny thorn-like pointed tip. Tuba analis broad, narrowed distally; scaphium very thin, weakly sclerotized. Tegumen short but broad, with arms fused in distal two thirds. Vinculum elongate, of equal length with tegumen, with thin arms connected distally by membranous commissure. Juxta trapezoid with two short narrowly triangular lateral processes apically. Valva moderately broad, with almost parallel margins and somewhat narrowed and rounded apex. Sacculus very narrow basally and strongly dilated distally. Distal saccular process elongate, reaching the valva tip, curved dorsally and pointed apically. Aedeagus elongate and narrow, with short and rounded coecum and slightly convex ventral wall medially. Vesica shorter and ca. 2 times broader than aedeagus, with short bilobate diverticulum laterally and long and narrow almost straight cornutus ventrally. Vesica ejaculatorius scobinated basally, projected distally. + +Female is unknown. + + + +Distribution +. The new species is known to date from western +Sichuan Province +of +China +only. + + + + +Etymology +. The specific epithet refers to the +type +locality. + + + + \ No newline at end of file diff --git a/data/38/76/9D/38769D1BFFB7FF921BCCFD8A24D0D526.xml b/data/38/76/9D/38769D1BFFB7FF921BCCFD8A24D0D526.xml new file mode 100644 index 00000000000..92a4f879978 --- /dev/null +++ b/data/38/76/9D/38769D1BFFB7FF921BCCFD8A24D0D526.xml @@ -0,0 +1,144 @@ + + + +Two new species of Manulea Wallengren, 1863 from southwestern China and northern Vietnam (Lepidoptera: Erebidae: Arctiinae: Lithosiini) + + + +Author + +Volynkin, Anton V. +0000-0001-9447-4925 +Altai State University, Lenina Avenue, 61, RF- 656049, Barnaul, Russia & monstruncusarctia @ gmail. com; https: // orcid. org / 0000 - 0001 - 9447 - 4925 +monstruncusarctia@gmail.com + + + +Author + +Saldaitis, Aidas +0000-0003-0999-3996 +Nature Research Centre, Akademijos str., 2, LT- 08412, Vilnius- 21, Lithuania & saldrasa @ gmail. com; https: // orcid. org / 0000 - 0003 - 0999 - 3996 +saldrasa@gmail.com + +text + + +Zootaxa + + +2021 + +2021-06-24 + + +4991 + + +2 + + +389 +397 + + + +journal article +5538 +10.11646/zootaxa.4991.2.12 +da3a8e32-ba5c-4043-90c3-909cd8ceff35 +1175-5326 +5030434 +DA474873-9729-4F7A-9CEE-875F9397F1BD + + + + + + +Genus + +Manulea +Wallengren, 1863 + + + + + + + + +Manulea +Wallengren, 1863 + +, +Wiener entomologische Monatschrift +, 7: 145, 146. + + + + +Type +species: + +Lithosia gilveola +Ochsenheimer, 1810 + +(a junior synonym of + +Phalaena palliatella +Scopoli, 1763 + +), by subsequent designation by +Moore (1878) +. + + + + +Diagnosis +. The genus was characterized and compared with + +Eilema + +in details by +Dubatolov & Zolotuhin (2011) +. No autapomorphies can be recognized, but in the male genitalia, the combination of the following features is characteristic for the genus: (1) the vinculum is strongly elongate, with thin and weakly sclerotized arms, not forming a saccus, with membranous intravincular area bearing one or two bunches of androconial scales; (2) the valva has a long and wide dorsal part with thin costa lacking processes; (3) the sacculus is relatively narrow and having an elongate, thorn-like distal process well separated from the dorsal part of the valva; (4) the aedeagus vesica broad and bearing few robust cornuti. The similar structure of the vinculum is also known in several other genera, namely the Eurasian + +Eilema + +, + +Tarika +Moore + +, + +Collita +Moore + +, and the African + +Lepidilema +Aurivillius + +, + +Dimorphilema +Krüger + +, + +Syntemnilema +Krüger + +and + +Lophilema +Aurivillius + +, but all these genera differ from each other by their valva structures. In the female genitalia, the large appendix bursae (in comparison to the corpus bursae) is characteristic. + + + + \ No newline at end of file diff --git a/data/38/76/9D/38769D1BFFB7FF971BCCFB44230CD563.xml b/data/38/76/9D/38769D1BFFB7FF971BCCFB44230CD563.xml new file mode 100644 index 00000000000..5382ce99e4e --- /dev/null +++ b/data/38/76/9D/38769D1BFFB7FF971BCCFB44230CD563.xml @@ -0,0 +1,375 @@ + + + +Two new species of Manulea Wallengren, 1863 from southwestern China and northern Vietnam (Lepidoptera: Erebidae: Arctiinae: Lithosiini) + + + +Author + +Volynkin, Anton V. +0000-0001-9447-4925 +Altai State University, Lenina Avenue, 61, RF- 656049, Barnaul, Russia & monstruncusarctia @ gmail. com; https: // orcid. org / 0000 - 0001 - 9447 - 4925 +monstruncusarctia@gmail.com + + + +Author + +Saldaitis, Aidas +0000-0003-0999-3996 +Nature Research Centre, Akademijos str., 2, LT- 08412, Vilnius- 21, Lithuania & saldrasa @ gmail. com; https: // orcid. org / 0000 - 0003 - 0999 - 3996 +saldrasa@gmail.com + +text + + +Zootaxa + + +2021 + +2021-06-24 + + +4991 + + +2 + + +389 +397 + + + +journal article +5538 +10.11646/zootaxa.4991.2.12 +da3a8e32-ba5c-4043-90c3-909cd8ceff35 +1175-5326 +5030434 +DA474873-9729-4F7A-9CEE-875F9397F1BD + + + + + + + +Manulea lienquan + +sp. nov. + + + + + + +( +Figs 1–6 +, +17–19 +, +24, 25 +) + + + + +Type material +. + + +Holotype + +( +Figs 1 +, +17 +): male, “N-Vietnam / +Tonkin +, Mt. Fan-si-pan ( +Nord +), +Cha-pa +, +Nebelwald +[cloud forest] ( +22.15ˊN +103.45ˊE +) + +2.–4.III.1995 + +, + +2400m + +, leg. +Dr. +R +. Brechlin”, gen. slide +No. +: +ZSM +Arct. +2020-158 (prepared by +Volynkin +) ( +MWM +/ +ZSM +). + + + + + +Paratypes + +. + +VIETNAM + +: +3 males +, +4 females +, the same data as in the +holotype +, gen. slide +No. +: +ZSM + + +Arct. +2020- 159 (female) (prepared by +Volynkin +) ( +MWM +/ +ZSM +) + +; + + +CHINA + +: +2 males +, +1 female +, +W + + +Sichuan +, + +10 km +Tianquan + +, H- + +880m + +, +N30°00.456ˊ +E102°45.277ˊ +, + +23.iv.2005 + +, +Floriani +& +Saldaitis +, gen. slide +Nos. +: +AV6410 +, +AV6411 +(males) + +, + +AV6412 +(female) (prepared by +Volynkin +) + +( +AFM +). + + + + +Diagnosis +. The female of the new species is very similar externally to + +M. postmaculosa + +, but the male is distinguished by the somewhat more convex costal margin of the forewing with the diffuse black spots, whereas the costal margin is more smoothly curved and the black spots are distinct in + +M. postmaculosa + +. The male genital capsule of + +M. lienquan + +is similar to that of + +M. postmaculosa + +but differs by the less elongate juxta, the more elongate vinculum, the somewhat less elongate valva with a more rounded costal margin, and the conspicuously less elongate and weaker distal saccular process. The aedeagus of the new species has a smaller coecum than in + +M. postmaculosa + +. The vesica of + +M. lienquan + +differs from that of + +M. postmaculosa + +by the twisted main chamber which is much broader than in + +M. postmaculosa + +, lacks a lateral diverticulum (present in + +M. postmaculosa + +) and bears elongate clusters of a shortly spinulose scobination (absent in + +M. postmaculosa + +). Additionally, the terminal cornutus of the new species is much thinner and has a less dilated distal section than that of + +M. postmaculosa + +. The female genitalia of + +M. lienquan + +are distinguished by the membranous medial and anterior sections of the corpus bursae which are sclerotized in + +M. postmaculosa + +. The appendix bursae of the new species is weakly gelatinous and wrinkled whereas that of + +M. postmaculosa + +is sclerotized inside and has thick gelatinous outer walls. The posterior section of the corpus bursae of + +M. lienquan + +is sclerotized laterally whereas in + +M. postmaculosa + +it is evenly weakly gelatinous. The anterior section of the corpus burse of + +M. lienquan + +is much wider and lacking a signum whereas it is much smaller and bearing a small round signum in + +M. postmaculosa + +. + + + + +FIGURES 1–8 +. + +Manulea +spp. + +: adults. Depositories of the specimens: 1, 2, 4 and 5 in MWM/ZSM; 3 and 6–8 in AFM. + + + + +FIGURES 9–16 +. + +Manulea +spp. + +: adults. Depositories of the specimens: 9–11 and 13–15 in MWM/ZSM; 12 in EIHU (photo by V.V. Zolotuhin, courtesy by V.V. Dubatolov); 16 in NHMUK (© The Trustees of NHMUK). + + + + +Description +. +External morphology of adults +( +Figs 1–6 +). Forewing length +15–17 mm +in males and +16–18 mm +in females. Sexual dimorphism moderately expressed: male has longer cilia on antennae and paler forewing with less elongate apex, grey suffusion and an additional diffuse black spot medially while female has monotonous forewing with only one black spot at anal margin. Head and thorax from ochreous brown to deep-brown. Abdomen ochreous brown, with a bunch of ochreous hair-like scales distally in male. Forewing elongate with strongly convex costal margin and elongate apex. Forewing ground colour varies from ochreous brown to deep-brown in males and deep-brown in females; male with two diffuse black spots and grey suffusion medially; female with one distinct black spot at anal margin medially. Hindwing monotonous ochreous yellow. +Male genitalia +( +Figs 17–19 +). Uncus elongate, narrow and straight basally and curved and dilated distally, with tiny thorn-like pointed tip. Tuba analis broad, narrowed distally; scaphium thin, weakly sclerotized. Tegumen short but broad, with arms fused medially and distally. Vinculum elongate, longer than tegumen, with thin arms connected distally by thinner commissure. Juxta trapezoid with short triangular apical protrusion. Valva relatively broad, with rounded costal margin and apex. Sacculus narrow, dilated distally, with a small dentate tubercle at the base of distal process. Distal saccular process relatively short, not reaching the valva tip, curved dorsally and pointed apically. Aedeagus large, wide, with short rounded coecum. Vesica very broad, twisted, with elongate cluster of shortly spinulose scobination along its axis and elongate subapical diverticulum projected dorsally and bearing a cluster of numerous tiny denticles apically. Terminal cornutus dilated basally, elongate and curved medially, with dilated, arrowhead-shaped tip. Vesica ejaculatorius scobinated basally, projected distally. +Female genitalia +( +Figs 24, 25 +). Papillae anales broadly trapezoid with rounded corners, weakly setose. Apophyses elongate and thin, equal in length. Ostium bursae wide. Antevaginal plate broadly elliptical. Ductus bursae broadly tubular, somewhat curved medially, elongate, membranous. Posterior section of corpus bursae wide, with sclerotized right side and membranous left side with appendix bursae originating from it. Anterior section of corpus bursae broad, sack-like, membranous. Appendix bursae broadly conical with rounded apex, weakly gelatinous and wrinkled, projecting laterally. + + + + +Distribution +. The species is known from North +Vietnam +( +Lao Cai Province +) and +Sichuan Province +of +China +. The records of + +M. postmaculosa + +from other provinces of +China +( +Zhejiang +, +Fujian +, +Guangdong +) (Daniel 1953; +Fang 2000 +) probably also belong to + +M. lienquan + +but require clarification. + + + + +Etymology +. In Vietnamese, ‘liên quan’ means ‘related’. The specific epithet refers to the close relationship of the new species and + +M. postmaculosa + +. + + + + \ No newline at end of file diff --git a/data/38/77/1F/38771FA974569973E490D626894FF349.xml b/data/38/77/1F/38771FA974569973E490D626894FF349.xml new file mode 100644 index 00000000000..d1b8983ab3e --- /dev/null +++ b/data/38/77/1F/38771FA974569973E490D626894FF349.xml @@ -0,0 +1,134 @@ + + + +A revision of the genus Arenivaga (Rehn) (Blattodea, Corydiidae), with descriptions of new species and key to the males of the genus + + + +Author + +Hopkins, Heidi + +text + + +ZooKeys + + +2014 + +384 + + +1 +256 + + + + +http://dx.doi.org/10.3897/zookeys.384.6197 + +journal article +http://dx.doi.org/10.3897/zookeys.384.6197 +1313-2970-384-1 +832EF8274642416895252C2AD202EB9B +832EF8274642416895252C2AD202EB9B + + + + +Arenivaga nalepae +sp. n. +Figures 111-113 + + + +Type locality. +USA, California, Riverside Co., Box Canyon. + + +Material examined. + +Holotype: ♂ in LACM labeled "CALIF., Riverside Co., Box Canyon, Mecca Hills, 600 ft. el., 12 Sept. 1986, J P & KES Donahue" "HOLOTYPE +Arenivaga nalepae +Hopkins, 2012" [red label with black border]. + + +Paratypes (73): USA: CA, Riverside Co., Box Canyon, Mecca Hills, 9/12/1986, 600 ft., JP & KES Donahue (14, LACM); CA, Imperial Co., Imperial Valley, near Wister, 10/27/1990, minus 75 ft., JP & KES Donahue, T9S R13E Sec.35, #149799 (1, LACM); CA, Riverside Co., Lamb Canyon, 2 mi. NW of Gilman Hot Springs, 3/7-11/27/1988, 1500 ft., FG Andrews, Pit trap (1, CSCA); CA, Riverside Co., Painted Canyon, 9/13/1979-1/7/1979, FG Andrews, E.glycol pit trap in desert wash (1, CSCA); CA, Riverside Co., Pinyon Flat, 8/5/1966, CA & MJ Tauber (1, EMEC); CA, Riverside Co., S side of Orocopia Mts., 3/25/1990, 900 ft., JP & KB Donahue,T7S R13B SW 1/4S.30, #2911 (1, LACM); CA, San Diego Co., Borrego Springs, 11/21/1958, JW Baker Jr., Black light trap, 58K25-1 (1, CSCA); CA, Riverside Co., Chiriaco Pass, 9/18/1971 (2, UCRC); CA, Imperial, 13 mi. NW of Glamis, 10/9/1993, 33.06.3N 115.15.3W, 250 ft., RR & C Snelling, black light (1, LACM); CA, Colton(?), 9/?/1949, O Cluh(?) (1, UCRC); CA, Fresno Co., Waltham Creek, 4 mi W of Coalinga, 8/28/1952, Leech & Green, dry bed (1, CAS); CA, San Bdno. Co., Cajon Wash, 8/4/40, 2000', Collected by J. C. vonBloeker (1, LACM); CA, Los Angeles Co., Black Butte, Antelope Valley, 8/22/1959, G Sphon (3, LACM); CA, LA Co., Black Butte, Antelope Valley, 7/25/1959, G Sphon, one specimen genitalia incomplete (5, LACM); CA, Inyo Co., Dunmovin, 9/6/1948, SA Sher, + +Arenivaga +erratica + +Rehn det. HF Strohecker 1953 (1, USNM); CA, Los Angeles Co., Whitehorn Picnic Area, Angeles NF, 8/22/1959, JA Honey (1, LACM); CA, Los Angeles, 6 mi. W of Lancaster, 10/3-5/1960, JA Chemsak (1, EMEC); CA, Kern Co., 8/29/1949, McKittrick, [one specimen missing head] (3, LACM); CA, Boron, 8/9/1959, J Helfer, black dot (1, USNM); CA, Los Angeles Co., Juniper Hills, 8/26/1973, A.V. Evans (1, LACM); CA, Kern Co., 4 mi NE of Mohave, 9/17/1966, TR Haig (6,CSCA); CA, Kern Co., Red Rock Canyon SP, Ricardo Ranger Station, 8/31-9/1/1991, 2700 ft., JP Donahue T9S R37E Sec.34,#24,431 (3, LACM); CA, Kern Co., Bakersfield, 4/6/1981, M Bock (1, LACM); CA, Kern Co., Bakersfield, 8/?/1954, R Smith, Cal.Dept.Agr.59H14-13, ex building (2,CSCA); CA, Fresno Co., Ciero Hills 18 air mi. SW of Mendota, 3/16/1975, J.T.Doyen, at light (2,EMEC); CA, Kings Co., Kettleman, 8/29/1972, L Bookout, +Arenivaga +sp. Det.AR Hardy 1972, Cal.Dept.Agr.37260, 7255-24, black light (2,CSCA); CA, Kern Co., near Buttonwillow, 9/27/1962, JR Anderson, ex burrow of Citellus beecheyi (1, EMEC); CA, Inyo Co., Saline Valley Salt Marsh, 1060', 7/1/1976, D. Giuliani, collected at blacklight (1, CSCA); CA, Inyo Co., Inyo Mts., Lead Canyon, 9/2/1976, 6-6500 ft., D Giuliani, BLM Survey, Inyo Co. Saline Valley 1976 site 3 (3, LACM); CA, Inyo Co., Eureka Valley Dunes, 9/4/1975, D Giuliani (3, CSCA); CA, Inyo Co., Eureka Valley Dunes, 7/13/1975, Andrews & Hardy (1, CSCA); NV, Mercury, 8/14/1964, 1BB25M(T) (1, USNM); AZ, Yuma Co., nr. Tacna, on dunes, night, 12/16/2010, +32.696N +, +113.79W +, 148 m, AD Smith (3, HEH). MEXICO: BC, San Felipe, 6/15/1952, Cazier, Gertsch & Schrammel (1, AMNH). All paratypes labeled "Paratype +Arenivaga nalepae +Hopkins 2012" [blue label with black border]. + + + +Etymology. +The name is a noun in the genitive case. This species is named for Christine Nalepa, who loves cockroaches, encourages that love in others, and co-authored "Cockroaches: Ecology, Behavior and Natural History", a book that had a profound effect on me. + + +Distribution. +This species is distributed from Saline Valley Salt Marsh in its northern and western extents to San Felipe, Baja California Norte, Mexico in its southern and eastern extents. See Fig. 113. + + +Diagnosis. + +Arenivaga nalepae +sp. n. is average in size and coloration for +Arenivaga +. It can be mistaken phenotypically for many other species, and its genitalia closely resemble that of +Arenivaga belli +, with whom it is probably closely related. The shape of the hook-shaped lobe on the right dorsal phallomere and the overall proportions of the right ventral phallomere are two distinguishing characters of this species. See Figs 112 and 31. + + + +Description. +Male.Measurements. Holotype TL = 20.4 mm, GW = 8.8 mm, PW = 6.22 mm, PL = 4.08 mm, TL/GW = 2.32, PL/PW = 0.65. EW = 0.25 mm; OW = 0.25 mm. Among paratypes range of TL 15.9-22.7 mm; range of GW 6.9-11.0 mm; range of PW 4.83-7.75 mm; range of PL 3.43-4.61 mm. + +Head. Two ocelli very large, ovoid and protruding (0.5 +x +0.4 mm), surrounded by waxy beige>0.1 mm border; vertex dark brown with small ridges in rays around upper apices of eyes and extending onto ocellar tubercles; interocellar space concave, dark brown with central medium brown dimple and two deep set medium brown dimples medial to inner apex of ocelli. Posterior frons pale orange-brown fading to waxy white towards clypeus, concave; anterior frons waxy white, bulbous; broad flat waxy white anteclypeus. See Fig. 111d. + +Pronotum. Pronotum translucent, waxy beige; dorsal surface of pronotum with short fine brown setae laterally and anteriorly; pronotal pattern orange-brown "panther face" with little discernible detail; slight lateral aura. See Fig. 111c. + +Body +. Wing brace present. Two tarsal claws present. Legs and body light orange-brown, darker maculation laterally on each sternite; subgenital plate with darker orange-brown border; strongly asymmetrical with rounded apices. See Fig. 111b. + +Forewings. Wings extended well beyond abdominal apex (~40% of wing length); light beige with occasional orange-brown blotches depending on specimen; surface translucent with slight sheen. See Fig. 111a. +Genitalia. Right dorsal phallomere composed of bulbous lightly sclerotized hook-shaped lobe, articulated with right ventral phallomere on lateral side; central field slightly sclerotized; medial margin heavily sclerotized, extending into smooth spine near distal end. Small central sclerite flat and finely punctate with posteriorly projecting, shagreened crescent in which dorsal arm of crescent is more prominently raised and toothed than ventral arm; right ventral phallomere extends from articulation to form rounded punctate structure at posterior apex but with shagreened corrugations at anterior apical end, followed by smaller offset shagreened projection and then by rounded concave arm extending beyond depth of rest of phallomere. Folded anterior portion of left phallomere setose, otherwise unmodified. Genital hook with long extension to pointed head with slight concavity on short hook; arm has distinct bend. See Fig. 112. + + +Figure 111. +Arenivaga nalepae +a dorsal habitus b ventral habitus c pronotum d head. + + + + +Figure 112. +Arenivaga nalepae +, genitalia: a) right dorsal phallomere b right ventral phallomere c small central sclerite d genital hook. Arrow(s) indicate diagnostic characters (see text). + + + + +Figure 113. +Arenivaga nalepae +, distribution. + + + + +Habitat and natural history. +This species is found in varied habitat from seashore to mountains to inland sand dunes and lakeshores. All other life history elements remain unobserved. + + + \ No newline at end of file diff --git a/data/38/77/77/38777768BBFB97C017E54DCAE6035908.xml b/data/38/77/77/38777768BBFB97C017E54DCAE6035908.xml new file mode 100644 index 00000000000..04fb7eeb966 --- /dev/null +++ b/data/38/77/77/38777768BBFB97C017E54DCAE6035908.xml @@ -0,0 +1,62 @@ + + + +The Formicidae (Hymenoptera) of Fennoscandia and Denmark. + + + +Author + +Collingwood, C. A. + +text + + +Fauna Entomologica Scandinavica + + +1979 + +8 + + +1 +174 + + + + +http://antbase.org/ants/publications/6175/6175.pdf + +journal article +6175 + + + + +Genus +Crematogaster +Lund, 1831 + + + + +Crematogaster +Lund, 1831:132. + + + + +Type-species: +Formica scutellaris Olivier +, 1791. + + + +All castes have the postpetiole attached to the dorsum of the first gaster segment. In the worker the cordate gaster is frequently carried uptilted and most species discharge a defensive deterrent fluid from the apical orifice, the sting being weak and atrophied. The male has very short antennal scapes, not longer than the two following funiculus segments. + + +This is a genus with many hundreds of species spread over the tropics and subtropics with a few palaearctic species none of which are endemic in North Europe. + + + \ No newline at end of file diff --git a/data/38/77/E0/3877E0640960FFB241AC5520C1869D0D.xml b/data/38/77/E0/3877E0640960FFB241AC5520C1869D0D.xml new file mode 100644 index 00000000000..9bd8d488072 --- /dev/null +++ b/data/38/77/E0/3877E0640960FFB241AC5520C1869D0D.xml @@ -0,0 +1,168 @@ + + + +New data on the genus Belyta Jurine, 1807 (Hymenoptera: Diapriidae, Belytinae) from Iran + + + +Author + +Izadizadeh, M. + + + +Author + +Talebi, A. A. + + + +Author + +Chemyreva, V. G. + + + +Author + +Farahani, S. + + + +Author + +Kazerani, F. + + + +Author + +Ameri, A. + +text + + +Far Eastern Entomologist + + +2023 + +2023-02-28 + + +471 + + +1 +18 + + + + +http://dx.doi.org/10.25221/fee.471.1 + +journal article +293143 +10.25221/fee.471.1 +3bd3e8b4-a0b1-419c-b415-bbba75cab956 +2713-2196 +7616360 +BD6B6967-8787-4701-A9B5-EBF4CC19F7D3 + + + + + + + +Belyta bicolor +Jurine, 1807 + + + + + + + +Figs 9–14 + + + + +MATERIAL EXAMINED ( +6 ♂ +). +Gilan Province +: +Amlash +( +36°58′31″ N +, +50°07′03.1″ E +, + +1380 m + +a.s.l), + +25.VI 2018 + +, +6 ♂ +, leg. +F. Kazerani +( +TMUC +, +RIRF +). + + + + +DIAGNOSIS. +Male +( +Fig. 9 +). Body length +3.2–3.5 mm +; face smooth and pubescent ( +Fig. 10 +) head in dorsal view transverse, 1.5 times as wide as long, smooth and pubescent ( +Fig. 11 +); POL 0.9 times as long as OOL ( +Fig. 11 +); antenna slender; A3 basally with emargination, reaching 0.35 of this segment length ( +Fig. 12 +); A4 3.0 times as long as wide; epomia strong; mesoscutum, convex and pubescent; anterior scutellar pit subsquare; scutellum convex and pubescent; fore wing length 2.7–3.0 mm; marginal vein 0.8–1.0 times as long as radial cell ( +Fig. 13 +); dorsal area of propodeum smooth and with sparse setae; median propodeal keel widely forked ( +Fig. 14 +); petiole in dorsal view 1.5–1.8 times as long as wide and with longitudinal keels ( +Fig. 14 +); T2 anteriorly with a median groove and laterally with some striations. + + + + +DISTRIBUTION. +Iran +(new record); +Czech Republic +, +England +, +Germany +, +Hungary +, +Sweden +, +Switzerland +( +Macek, 1996 +). + + + + \ No newline at end of file diff --git a/data/38/77/E0/3877E0640961FFBE41AC5479C2D29926.xml b/data/38/77/E0/3877E0640961FFBE41AC5479C2D29926.xml new file mode 100644 index 00000000000..575202b4f29 --- /dev/null +++ b/data/38/77/E0/3877E0640961FFBE41AC5479C2D29926.xml @@ -0,0 +1,989 @@ + + + +New data on the genus Belyta Jurine, 1807 (Hymenoptera: Diapriidae, Belytinae) from Iran + + + +Author + +Izadizadeh, M. + + + +Author + +Talebi, A. A. + + + +Author + +Chemyreva, V. G. + + + +Author + +Farahani, S. + + + +Author + +Kazerani, F. + + + +Author + +Ameri, A. + +text + + +Far Eastern Entomologist + + +2023 + +2023-02-28 + + +471 + + +1 +18 + + + + +http://dx.doi.org/10.25221/fee.471.1 + +journal article +293143 +10.25221/fee.471.1 +3bd3e8b4-a0b1-419c-b415-bbba75cab956 +2713-2196 +7616360 +BD6B6967-8787-4701-A9B5-EBF4CC19F7D3 + + + + + + + +Belyta depressa +Thomson, 1858 + + + + + + + +Figs 15–21 + + + + +MATERIAL EXAMINED ( +13 ♀ +, +230 ♂ +). +Alborz Province +: Chalous Road, Shahrestanak ( +35°58′16.26″ N +, +51°21′25.80″ E +, +2225 m +a.s.l.), + +06.VII 2010 + +, +1 ♂ +( +TMUC +); + +15.VI 2010 + +, +1 ♀ +, +4 ♂ +( +TMUC +); + +22.VI 2020 + +, +2 ♂ +( +TMUC +); + +14.VII 2010 + +, +1 ♀ +( +TMUC +); + +28.VII 2010 + +, +1 ♂ +( +TMUC +); +Chalous Road +, +Sarziarat +( +35°55′10.38″ N +, +51°06′51.24″ E +, + +1980 m +a.s.l. + +), + +14.VII 2010 + +, +1 ♂ +( +TMUC +); +Shahriar +( +35°40′08.10″ N +, +50°56′56.64″ E +, + +1168 m +a.s.l. + +), + +24.VIII 2010 + +, +1 ♂ +( +TMUC +); +Chalous Road +, +Arangeh +( +35°55′07 20″ N +, +51°05′09.24″ E +, + +1891 m +a.s.l. + +), + +31.VIII 2010 + +, +7 ♂ +( +TMUC +). +Qazvin Province +: +Zereshk Road +( +36°21′39.72″ N +, +50°03′55.56″ E +, + +1541 m +a.s.l. + +), + +09.VI 2011 + +, +2 ♂ +( +TMUC +); + +06.VII 2011 + +, +2 ♂ +( +TMUC +); +Zereshk Road +( +36°25′39.36″ N +, +50°06′36.90″ E +, + +1997 m +a.s.l. + +), + +06.VII 2011 + +, +1 ♀ +, +5 ♂ +( +TMUC +); + +26.VII 2011 + +, +1 ♀ +, +9 ♂ +, leg. +A. Nadimi +( +TMUC +). +Gilan Province +: +Roudsar +, +Rahimabad +, +Orkom +( +36°45′44.34″ N +, +50°18′11.88″ E +, + +1201 m +a.s.l. + +), + +26.IV 2010 + +, +1 ♂ +( +TMUC +); + +14.VI 2010 + +, +2 ♂ +( +TMUC +); + +06.VII 2010 + +, +4 ♂ +( +TMUC +); + +26.VII 2010 + +, +2 ♂ +( +TMUC +); +Roudsar +, +Rahimabad +, +Ziaz +( +36°52′27.18″ N +, +50°13′24.78″ E +, + +490 m +a.s.l. + +), + +20.IX 2010 + +, +1 ♂ +( +TMUC +); +Roudsar +, +Rahimabad +, +Ghazichak +( +36°45′57.54″ N +, +50°19′35.22″ E +, + +1803 m +a.s.l. + +), + +13.IX 2010 + +, +1 ♀ +, +1 ♂ +( +TMUC +); + +25.X 2010 + +, +3 ♂ +( +TMUC +); +Roudsar +, +Rahimabad +, +Ghazichak +( +36°45′52.62″ N +, +50°20′01.08″ E +, + +1787 m +a.s.l. + +), + +19.IV 2010 + +, +1 ♂ +( +TMUC +); + +17.V 2010 + +, +2 ♂ +( +TMUC +); + +31.V 2010 + +, +4 ♂ +( +TMUC +); + +22.VI 2010 + +, +1 ♂ +( +TMUC +); + +28.VI 2010 + +, +4 ♂ +( +TMUC +); +Astaneh Ashrafiyeh +, +Eshman +kamachal ( +37°21′10.50″ N +, +49°57′56.16″ E +, + +2 m +a.s.l. + +), + +24.V 2010 + +, +1 ♀ +( +TMUC +); +Roudsar +, +Rahimabad +, +Ziaz +( +36°52′27.18″ N +, +50°13′24.78″ E +, + +490 m +a.s.l. + +), + +31.V 2010 + +, +6 ♂ +, leg. +M. Khayrandish +( +TMUC +); +Astara +, +Lavandevil forest +( +38°18′19″ N +, +48°42′57″ E +, + +873 m +a.s.l. + +), + +06.VI 2017 + +, +4 ♂ +( +TMUC +); + +08.VII 2017 + +, +6 ♂ +( +TMUC +); + +07.VIII 2017 + +, +2 ♂ +( +TMUC +); + +26.XI 2017 + +, +1 ♀ +, leg. +S. Farahani +( +TMUC +); +Rezvan Shahr +( +37°31′00″ N +, +49°02′07″ E +, + +199 m + +a.s.l), + +13.V 2018 + +, +3 ♂ +( +TMUC +); +Shafaroud forest +( +37°28′18ʺ N +, +48°49′23ʺ E +, + +1114 m + +a.s.l), + +25.VI 2018 + +, +16 ♂ +( +RIRF +); + +26.VIII 2018 + +, +2 ♂ +( +TMUC +); + +19.X 2018 + +, +4 ♂ +, leg. +F. Kazerani +( +TMUC +). +Mazandaran Province +: +Noor +, +Chamestan +, +Tangehvaz +( +36°21′55.02″ N +, +52°06′10.74″ E +, + +692 m +a.s.l. + +), + +09.V 2011 + +, +5 ♂ +( +TMUC +); + +25.V 2011 + +, +1 ♀ +, +4 ♂ +( +TMUC +); + +26.VII 2011 + +, +2 ♂ +( +TMUC +); + +26.IX 2011 + +, +3 ♂ +( +TMUC +); +Noor +, +Chamestan +, +Tangehvaz +( +36°18′51.42″ N +, +52°07′48.00″ E +, + +1359 m +a.s.l. + +), +25.V 2011 +, +2 ♂ +; + +13.VII 2011 + +, +3 ♂ +( +TMUC +); + +05.IX 2011 + +, +1 ♂ +( +TMUC +); +Noor +, +Chamestan +, +Joorband +( +36°26′17.28″ N +, +52°07′16.62″ E +, + +272 m +a.s.l. + +), + +04.XI 2011 + +, +2 ♂ +, leg. +M. Khayrandish +( +TMUC +); +Alikola +(36˚13′14″ N, 53˚39′24″ E, + +1626 m +a.s.l. + +), + +15.VI 2016 + +, +1 ♂ +, leg. +S. Farahani +( +TMUC +); +Neka forest +( +36°30′00.4″ N +, +53°27′14.2″ E +, + +828 m + +a.s.l), +24.VII 2018 +, +3 ♂ +; + +20.X 2018 + +, +11 ♂ +( +TMUC +); +Neka forest +( +36°21′43.03″ N +, +53°32′56.7″ E +, + +1495 m + +a.s.l), + +25.VII 2018 + +, +21 ♂ +( +TMUC +); +Neka forest +( +36°34′49.2″ N +, +53°27′95.6″ E +, + +465 m + +a.s.l), + +16.V 2018 + +, +1 ♀ +, +1 ♂ +( +RIRF +); + +24.VII 2018 + +, +9 ♂ +( +RIRF +); + +20.X 2018 + +, +2 ♂ +( +TMUC +); +Kheyroud Kenar +( +36°34′36.23ʺ N +, +51°34′37.94ʺ E +, + +722 m + +a.s.l), + +26.VI 2018 + +, +1 ♀ +, +3 ♂ +( +RIRF +); + +24.VII 2018 + +, +4 ♂ +( +TMUC +); + +28.VIII 2018 + +, +1 ♂ +( +TMUC +); + +21.X 2018 + +, +1 ♂ +( +TMUC +); +Galanderoud +( +36°26′56″ N +, +51°51′20″ E +, + +1407 m + +a.s.l), + +24.VII 2018 + +, +3 ♂ +( +TMUC +). +Golestan Province +: +Shast Kola forest +( +36°44′10.83″ N +, +54°24′11.23″ E +, + +754 m + +a.s.l), + +26.VI 2019 + +, +1 ♀ +, +2 ♂ +( +TMUC +); + +28.VII 2019 + +, +34 ♂ +( +TMUC +); + +12.X 2019 + +, +11 ♂ +, leg. +F. Kazerani +( +RIRF +); Deraz-No ( +36°40′06″ N +, +54°08′03″ E +, + +2179 m + +a.s.l), + +06.X 2016 + +, +1 ♂ +, leg. +S. Farahani +( +TMUC +). + + + + +Figs 15–21. + +Belyta depressa +Thomson, 1859 + +: female (15–18) and male (19–21). 15 – general habitus; 16 – head in frontal view; 17 – head in dorsal view; 18 – propodeum and basal part of metasoma; 19 – general habitus; 20 – base of antenna; 21 – fore wing. + + + + +DIAGNOSIS. +Female +( +Fig. 15 +). Body length +2.8–3.6 mm +; face smooth and pubescent ( +Fig. 16 +); head in dorsal view as long as wide, smooth and pubescent; POL 0.6–0.7 times as long as OOL ( +Fig. 17 +); A4-A14 transverse; epomia moderately prominent; mesoscutum and scutellum flat and pubescent; anterior scutellar pit reniform ( +Fig. 17 +); fore wing length +2.1–2.6 mm +; radial cell open ( +Fig. 21 +); marginal vein 0.4–0.6 times as long as its distance from basal vein; propodeum bare; median propodeal keel widely bifurcate ( +Fig. 18 +); petiole in dorsal view 1.2–1.4 times as long as wide, with coarsely sculpture ( +Fig. 18 +); T2 anteriorly with a median groove, grooves and sculpture laterally. +Male +( +Fig. 19 +): flagellomeres cylindrical, A3 basally with emargination reaching 0.5 of this segment length ( +Fig. 20 +). + + + + +DISTRIBUTION. +Iran +(new record); +Austria +, +Belgium +, +Czech Republic +, +Finland +, +France +, +Germany +, +Italy +, +Malta +, +Poland +, +Scotland +, +Slovakia +, +Sweden +( +Nixon, 1957 +; +Hellén, 1964 +; +Wall, 1993 +; +Macek, 1996 +; +Notton & Mifsud, 2019 +). + + + +BIOLOGY. Unknown. + + + \ No newline at end of file diff --git a/data/38/77/E0/3877E0640966FFB241AC546AC2D298F8.xml b/data/38/77/E0/3877E0640966FFB241AC546AC2D298F8.xml new file mode 100644 index 00000000000..3faac841e42 --- /dev/null +++ b/data/38/77/E0/3877E0640966FFB241AC546AC2D298F8.xml @@ -0,0 +1,611 @@ + + + +New data on the genus Belyta Jurine, 1807 (Hymenoptera: Diapriidae, Belytinae) from Iran + + + +Author + +Izadizadeh, M. + + + +Author + +Talebi, A. A. + + + +Author + +Chemyreva, V. G. + + + +Author + +Farahani, S. + + + +Author + +Kazerani, F. + + + +Author + +Ameri, A. + +text + + +Far Eastern Entomologist + + +2023 + +2023-02-28 + + +471 + + +1 +18 + + + + +http://dx.doi.org/10.25221/fee.471.1 + +journal article +293143 +10.25221/fee.471.1 +3bd3e8b4-a0b1-419c-b415-bbba75cab956 +2713-2196 +7616360 +BD6B6967-8787-4701-A9B5-EBF4CC19F7D3 + + + + + + + +Belyta abrupta +Thomson, 1858 + + + + + + + +Figs 1–8 + + + + +MATERIAL EXAMINED ( +25 ♀ +, +611 ♂ +). +Gilan Province +: +Astara +, +Lavandevil forest +( + +38°18′19″ +N + +, + +48°42′57″ +E + +, + +873 m +a.s.l. + +), + +06.VI 2017 + +, +2 ♂ +( +TMUC +); + +08.VII 2017 + +, +2 ♂ +( +TMUC +); + +07.VIII 2017 + +, +3 ♂ +( +TMUC +); + +05.IX 2017 + +, +1 ♂ +, leg. +S. Farahani +( +TMUC +); +Rezvan Shahr +( + +37°31′00″ +N + +, + +49°2′7″ +E + +, + +199 m + +a.s.l), + +13.V 2018 + +, +4 ♀ +, +15 ♂ +( +TMUC +); +Shafaroud forest +( + +37°28′18ʺ +N + +, + +48°49′23ʺ +E + +, + +1114 m + +a.s.l), + +25.VI 2018 + +, +2♀ +, +12 ♂ +( +TMUC +); + +26.VIII 2018 + +, +6 ♀ +, +44 ♂ +( +RIRF +); + +19.X 2018 + +, +5 ♀ +( +TMUC +). +Mazandaran Province +: +Kheyroud Kenar +( + +36°34′36.23ʺ +N + +, + +51°34′37.94ʺ +E + +, + +722 m + +a.s.l), + +24.VII 2018 + +, +2 ♂ +( +TMUC +); + +21.X 2018 + +, +3 ♂ +( +TMUC +); +Galanderoud +( + +36°26′56″ +N + +, + +51°51′20″ +E + +, + +1407 m + +a.s.l), + +28.VIII 2018 + +, +3 ♂ +( +TMUC +); + +21.X 2018 + +, +1 ♂ +( +TMUC +); +Neka forest +( + +36°30′00.4″ +N + +, + +53°27′14.2″ +E + +, + +828 m + +a.s.l), + +16.V 2018 + +, +16 ♂ +( +TMUC +); + +24.VII 2018 + +, +133 ♂ +( +TMUC +); + +29.VIII 2018 + +, +2 ♀ +, +36 ♂ +( +RIRF +); + +20.X 2018 + +, +54 ♂ +( +RIRF +); +Neka forest +( + +36°21′43.03″ +N + +, + +53°32′56.7″ +E + +, + +1495 m + +a.s.l), + +07.VII 2018 + +, +10 ♂ +( +TMUC +); + +25.VII 2018 + +, +4♀ +, +150 ♂ +( +TMUC +); +Neka forest +( +36°34′49.2″ N +, +53°27′95.6″ E +, + +465 m + +a.s.l), + +24.VII 2018 + +, +1 ♀ +, +10 ♂ +( +RIRF +). +Golestan Province +: +Shast Kola forest +( + +36° 44' 10.83" +N + +, + +54° 24' 11.23" +E + +, + +754 m + +a.s.l), + +26.VI 2019 + +, +67 ♂ +( +TMUC +); + +28.VII 2019 + +, +16 ♂ +, leg. +F. Kazerani +( +RIRF +); +Loveh forest +( + +37°20′43″ +N + +, + +55°40′40″ +E + +, + +753 m +a.s.l. + +), + +25.VII 2016 + +, +2 ♂ +( +TMUC +); + +03.XII 2016 + +, +1 ♀ +( +TMUC +); +Ali Abad +, +Zarin Gol village +( + +36°48′58″ +N + +, + +55°02′13″ +E + +, + +694 m +a.s.l. + +), + +26.VII 2016 + +, +2 ♂ +( +TMUC +); +Shast Kola forest +( + +36°45′29″ +N + +, + +54°23′12″ +E + +, + +424 m +a.s.l. + +), + +12.VI 2016 + +, +12 ♂ +( +RIRF +); + +03.VII 2016 + +, +15 ♂ +, leg. +S. Farahani +( +TMUC +). + + + + +Figs 1–8. + +Belyta abrupta +Thomson, 1858 + +: female (1–6) and male (7, 8). 1 – general habitus; 2 – head in frontal view; 3 – head in dorsal view; 4 – antenna; 5 – fore wing; 6 – propodeum and basal part of metasoma; 7 – fore wing; 8 – base of antenna. + + + + +DIAGNOSIS. +Female +( +Fig. 1 +): body length +3.3–3.5 mm +; face with sculpture ( +Fig. 2 +); head in dorsal view transverse, 1.4 times as wide as long, pubescent and with punctures ( +Fig. 3 +); POL 0.5 times as long as OOL ( +Fig. 3 +); flagellomeres subquadrate ( +Fig. 4 +); epomia strong; pronotal collar sculptured; mesoscutum flat, pubescent and sparse puncture; anterior scutellar pit small and bare; scutellum pubescent; fore wing length +2.7–3.1 mm +; radial cell open ( +Fig. 5 +); marginal vein very short, 0.25 times as long as its distance from basal vein ( +Fig. 5 +); propodeum smooth and shine, with sparse setae and median propodeal keel strong and forked ( +Fig. 6 +); petiole in dorsal view 1.6–1.8 times as long as wide, with longitudinal keels ( +Fig. 6 +); T2 anteriorly with a median groove, each side of median groove with short grooves ( +Fig. 6 +); metasoma apically truncate. +Male: +A3–A14 cylindrical, A3 basally with emargination, reaching 0.4 of this segment length ( +Fig. 8 +), radial cell close ( +Fig. 7 +). + + + + +DISTRIBUTION. +Iran +(new record); +Austria +, +Czech Republic +, +Finland +, +France +(including +Corsica +), +Germany +, +Italy +, +Slovakia +, +Sweden +, +Switzerland +( +Nixon, 1957 +; +Hellén, 1964 +; +Wall, 1993 +; +Macek, 1996 +). + + + +BIOLOGY. Unknown. + + + \ No newline at end of file diff --git a/data/38/77/E0/3877E0640966FFB4435F53CFC14C9E30.xml b/data/38/77/E0/3877E0640966FFB4435F53CFC14C9E30.xml new file mode 100644 index 00000000000..fdb28751862 --- /dev/null +++ b/data/38/77/E0/3877E0640966FFB4435F53CFC14C9E30.xml @@ -0,0 +1,111 @@ + + + +New data on the genus Belyta Jurine, 1807 (Hymenoptera: Diapriidae, Belytinae) from Iran + + + +Author + +Izadizadeh, M. + + + +Author + +Talebi, A. A. + + + +Author + +Chemyreva, V. G. + + + +Author + +Farahani, S. + + + +Author + +Kazerani, F. + + + +Author + +Ameri, A. + +text + + +Far Eastern Entomologist + + +2023 + +2023-02-28 + + +471 + + +1 +18 + + + + +http://dx.doi.org/10.25221/fee.471.1 + +journal article +293143 +10.25221/fee.471.1 +3bd3e8b4-a0b1-419c-b415-bbba75cab956 +2713-2196 +7616360 +BD6B6967-8787-4701-A9B5-EBF4CC19F7D3 + + + + + + +Genus + +Belyta +Jurine, 1807 + + + + + + + +Type +species: + +Belyta bicolor +Jurine, 1807 + +. + + + + +DIAGNOSIS. Body slender, rather flattened (2.0– +5.5 mm +); head orthognathous to hypognathous with strongly prominent antennal shelf; subantennal grooves distinct or reduced; mandibles short, asymmetrical with slightly overlapping tips; female antennae 15-segmented with transverse to submoniliform flagellomeres of equal width; male antenna 14-segmented with cylindrical flagellomeres and A3 modified; pronotum more or less elongate with wide pronotal collar; pronotal collar rugose, sometimes divided by median pit in two parts; mesoscutum flat in females, rather convex in males; notauli distinct; scutellum smooth along posterior margin, with single scutellar fovea of varying shape and size; fore wings with radial cell closed to open; stigmal vein oblique and form acute angle with the marginal vein; marginal vein shorter than its distance from basal vein; hind wing lanceolate with distinct basal cell; metascutellum with three low longitudinal keels; propodeum with median keel simple or bifurcate; petiole cylindrical, at least slightly longer than wide, on dorsal surface with longitudinal keels, or rugose sculpture ( +Nixon, 1957 +; +Kozlov, 1978 +; +Macek, 1996 +). + + + + \ No newline at end of file diff --git a/data/38/77/E0/3877E0640968FFB841AC5476C2D29AE4.xml b/data/38/77/E0/3877E0640968FFB841AC5476C2D29AE4.xml new file mode 100644 index 00000000000..d28d644685c --- /dev/null +++ b/data/38/77/E0/3877E0640968FFB841AC5476C2D29AE4.xml @@ -0,0 +1,265 @@ + + + +New data on the genus Belyta Jurine, 1807 (Hymenoptera: Diapriidae, Belytinae) from Iran + + + +Author + +Izadizadeh, M. + + + +Author + +Talebi, A. A. + + + +Author + +Chemyreva, V. G. + + + +Author + +Farahani, S. + + + +Author + +Kazerani, F. + + + +Author + +Ameri, A. + +text + + +Far Eastern Entomologist + + +2023 + +2023-02-28 + + +471 + + +1 +18 + + + + +http://dx.doi.org/10.25221/fee.471.1 + +journal article +293143 +10.25221/fee.471.1 +3bd3e8b4-a0b1-419c-b415-bbba75cab956 +2713-2196 +7616360 +BD6B6967-8787-4701-A9B5-EBF4CC19F7D3 + + + + + + + +Belyta validicornis +Thomson, 1858 + + + + + + + +Figs 41–46 + + + + +MATERIAL EXAMINED ( +7 ♂ +). +Alborz Province +: +Chalous Road +, +Arangeh +( +35°55′07.20″ N +, +51°05′09.24″ E +, + +1891 m +a.s.l. + +), + +08.VI 2010 + +, +1 ♂ +, leg. +A. Nadimi +( +TMUC +). +Golestan Province +: +Shast Kola forest +( +36°45′29″ N +, +54°23′12″ E +, + +424m +a.s.l. + +), + +03.VII 2016 + +, +1 ♂ +, leg. +S. Farahani +( +TMUC +). +Mazandaran Province +: +Kheyroud Kenar +( +36°34′36.23ʺ N +, +51°34′37.94ʺ E +, + +722 m + +a.s.l), + +24.VII 2018 + +, +2 ♂ +( +TMUC +); +Neka forest +( +36°30′00.4″ N +, +53°27′14.2″ E +, + +828 m + +a.s.l), + +27.VI 2018 + +, +1♂ +( +RIRF +); + +20.X 2018 + +, +2 ♂ +, leg. +F. Kazerani +( +RIRF +). + + + + +Figs 41–46. + +Belyta validicornis +Thomson, 1859 + +, male. 41 – general habitus; 42 – head in frontal view; 43 – head in dorsal view; 44 – base of antenna; 45 – fore wing; 46 – propodeum and base of metasoma. + + + + +DIAGNOSIS. +Male +( +Fig. 41 +). Body length +2.9–3.3 mm +; face smooth and pubescent ( +Fig. 42 +); head in dorsal view transverse, 1.6 times as wide as long; POL as long as OOL ( +Fig. 43 +); antenna slender, A3 with basal emargination, reaching 0.45 of this segment length; A4 3.0 times as long as wide ( +Fig. 44 +); epomia present; mesoscutum convex and pubescent; fore wing length +2.3–2.6 mm +; radial cell open ( +Fig. 45 +); marginal vein 0.45–0.55 times as long as its distance from basal vein; anterior scutellar pit semicircular ( +Fig. 46 +); scutellum convex and pubescent; propodeum smooth, with sparse setae, median propodeal keel widely bifurcate ( +Fig. 46 +); petiole in dorsal view 1.1–1.2 times as long as wide, with longitudinal keels ( +Fig. 46 +); T2 anteriorly with short striation. + + + + +DISTRIBUTION. +Iran +(new record); +Czech Republic +, +England +, +Finland +, +Germany +, +Hungary +, +Italy +, +Slovakia +, +Sweden +, +Switzerland +( +Nixon, 1957 +; +Wall, 1993 +; +Macek, 1996 +). + + + +BIOLOGY. Unknown. + + + \ No newline at end of file diff --git a/data/38/77/E0/3877E064096DFFBD41AC52A1C2D29A6C.xml b/data/38/77/E0/3877E064096DFFBD41AC52A1C2D29A6C.xml new file mode 100644 index 00000000000..5bd21b2175f --- /dev/null +++ b/data/38/77/E0/3877E064096DFFBD41AC52A1C2D29A6C.xml @@ -0,0 +1,365 @@ + + + +New data on the genus Belyta Jurine, 1807 (Hymenoptera: Diapriidae, Belytinae) from Iran + + + +Author + +Izadizadeh, M. + + + +Author + +Talebi, A. A. + + + +Author + +Chemyreva, V. G. + + + +Author + +Farahani, S. + + + +Author + +Kazerani, F. + + + +Author + +Ameri, A. + +text + + +Far Eastern Entomologist + + +2023 + +2023-02-28 + + +471 + + +1 +18 + + + + +http://dx.doi.org/10.25221/fee.471.1 + +journal article +293143 +10.25221/fee.471.1 +3bd3e8b4-a0b1-419c-b415-bbba75cab956 +2713-2196 +7616360 +BD6B6967-8787-4701-A9B5-EBF4CC19F7D3 + + + + + + + +Belyta rugosicollis +Kieffer, 1909 + + + + + + + +Figs 28–34 + + + + +MATERIAL EXAMINED ( +79 ♂ +). +Mazandaran Province +: +Noor +, +Chamestan +, +Tangehvaz +( +36°18′51.42″ N +, +52°07′48.00″ E +, + +1359 m +a.s.l. + +), + +13.VII 2011 + +, +1 ♂ +( +TMUC +); + +05.IX 2011 + +, +1 ♂ +( +TMUC +); + +26.IX 2011 + +, +2 ♂ +, leg. +M. Khayrandish +( +TMUC +); Kiasar, Haftkhal ( +36°17′19″ N +, +53°23′43″ E +, + +1624 m +a.s.l. + +), +3 ♂ +( +TMUC +). +Gilan Province +: Sowme'eh Sara, Gurab Zarmikh, Tanian ( +37°17′20″ N +, +49°05′54″ E +, + +252 m +a.s.l. + +), + +08.VII 2017 + +, +1 ♂ +( +TMUC +); + +05.IX 2017 + +, +1 ♂ +( +TMUC +); +Lavandevil forest +( +38°18′19″ N +, +48°42′57″ E +, + +873 m +a.s.l. + +), + +06.VI 2017 + +, +2 ♂ +, leg. +S. Farahani +( +TMUC +); +Shafaroud forest +( +37°28′18″ N +, +48°49′23″ E +, + +1114 m + +a.s.l), + +25.VI 2018 + +, +37 ♂ +( +RIRF +); + +26.VIII 2018 + +, +14 ♂ +( +TMUC +); + +19.X 2018 + +, +12 ♂ +( +TMUC +); Rezvan Shahr ( +37°31′00″ N +, +49°2′7″E +, + +199 m + +a.s.l), + +13.V 2018 + +, +2 ♂ +, leg. +F. Kazerani +( +RIRF +). +Golestan Province +: +Shamooshak forest +( +36°43′55″ N +, +54°16′53″ E +, + +492 m +a.s.l. + +), + +26.VII 2016 + +, +2 ♂ +( +TMUC +); +Tuskestan forest +( +36°46′33″ N +, +54°34′58″ E +, + +500 m +a.s.l. + +), + +26.X 2016 + +, +1 ♂ +, leg. +S. Farahani +( +TMUC +). + + + + +DIAGNOSIS. +Male +( +Fig. 28 +). Body length +3.1–3.3 mm +; face smooth and pubescent ( +Fig. 29 +), head in dorsal view transverse, 1.6 times as wide as long, smooth and pubescent ( +Fig. 30 +); POL 0.65 times as long as OOL; antenna slender; A3 basally with emargination, reaching 0.33 of this segment length ( +Fig. 31 +); A4 3.0 times as long as wide; epomia strongly prominent; mesoscutum and scutellum convex and pubescent; anterior scutellar pit subsquare; fore wing length +2.6–2.9 mm +; marginal vein 0.4–0.5 times as long as its distance from basal vein ( +Fig. 32 +); inner side of fore tibiae with three bristles ( +Fig. 33 +); dorsal area of propodeum smooth and with sparse setae; median propodeal keel widely forked ( +Fig. 34 +); petiole in dorsal view 1.7–1.9 times as long as wide, with longitudinal keels ( +Fig. 34 +); T2 anteriorly with a median groove and laterally with some striations. + + + + +Figs 28–34. + +Belyta rugosicollis +Kieffer, 1909 + +, male. 28 – general habitus; 29 – head in frontal view; 39 – head in dorsal view; 31 – base of antenna; 32 – fore wing; 33 – fore tibiae; 34 – propodeum and base of metasoma. + + + + +DISTRIBUTION. +Iran +(new record); +Austria +, +Czech Republic +, +England +, +France +, +Germany +, +Ireland +, +Slovakia +, +Sweden +, +Switzerland +( +Nixon, 1957 +; +Wall, 1967 +; +Macek, +1996). + +BIOLOGY. Unknown. + + + \ No newline at end of file diff --git a/data/38/77/E0/3877E064096DFFBF41AC5025C2D29874.xml b/data/38/77/E0/3877E064096DFFBF41AC5025C2D29874.xml new file mode 100644 index 00000000000..02c2a88c712 --- /dev/null +++ b/data/38/77/E0/3877E064096DFFBF41AC5025C2D29874.xml @@ -0,0 +1,183 @@ + + + +New data on the genus Belyta Jurine, 1807 (Hymenoptera: Diapriidae, Belytinae) from Iran + + + +Author + +Izadizadeh, M. + + + +Author + +Talebi, A. A. + + + +Author + +Chemyreva, V. G. + + + +Author + +Farahani, S. + + + +Author + +Kazerani, F. + + + +Author + +Ameri, A. + +text + + +Far Eastern Entomologist + + +2023 + +2023-02-28 + + +471 + + +1 +18 + + + + +http://dx.doi.org/10.25221/fee.471.1 + +journal article +293143 +10.25221/fee.471.1 +3bd3e8b4-a0b1-419c-b415-bbba75cab956 +2713-2196 +7616360 +BD6B6967-8787-4701-A9B5-EBF4CC19F7D3 + + + + + + + +Belyta elongata +Thomson, 1858 + + + + + + + +Figs 22–27 + + + + +MATERIAL EXAMINED. +Mazandaran Province +, +Neka forest +( +36°21′43.03″ N +, +53°32′56.7″ E +, + +1495 m + +a.s.l), + +27.VI 2018 + +, +2 ♂ +, leg. +F. Kazerani +( +TMUC +, +RIFR +). + + + + +DIAGNOSIS. +Male +( +Fig. 22 +). Body length +3.6–3.7 mm +; face with fine sculpture ( +Fig. 23 +); head in dorsal view transverse, 1.4 times as wide as long, smooth and densely pubescent ( +Fig. 24 +); POL 0.8 times as long as OOL; antenna slender; A3 basally with emargination, reaching 0.33 of this segment length; A4 3.5 times as long as wide ( +Fig. 25 +); mesoscutum and scutellum convex and pubescent; anterior scutellar pit large, semicircular; epomia strongly prominent; fore wing length +3.1– 3.3 mm +; marginal vein 0.5 times as long as its distance from basal vein; radial cell long, 2.8 times as long as marginal vein ( +Fig. 26 +); propodeum pubescent, median propodeal keel simple ( +Fig. 27 +); petiole in dorsal view 2.0–2.1 times as long as wide, with fine longitudinal keels ( +Fig. 27 +); T2 anteriorly with a median groove, each side of median groove with two short grooves. + + + + +DISTRIBUTION. +Iran +(new record); +Austria +, +Czech Republic +, +England +, +Finland +, +France +, +Germany +, +Ireland +, +Italy +, +Slovakia +, +Sweden +( +Nixon, 1957 +; +Hellén, 1964 +; +Wall, 1993 +: +Macek, 1996 +). + + + +BIOLOGY. Unknown. + + + \ No newline at end of file diff --git a/data/38/77/E0/3877E064096FFFBD41AC5088C0209EFD.xml b/data/38/77/E0/3877E064096FFFBD41AC5088C0209EFD.xml new file mode 100644 index 00000000000..b97e5069a7b --- /dev/null +++ b/data/38/77/E0/3877E064096FFFBD41AC5088C0209EFD.xml @@ -0,0 +1,462 @@ + + + +New data on the genus Belyta Jurine, 1807 (Hymenoptera: Diapriidae, Belytinae) from Iran + + + +Author + +Izadizadeh, M. + + + +Author + +Talebi, A. A. + + + +Author + +Chemyreva, V. G. + + + +Author + +Farahani, S. + + + +Author + +Kazerani, F. + + + +Author + +Ameri, A. + +text + + +Far Eastern Entomologist + + +2023 + +2023-02-28 + + +471 + + +1 +18 + + + + +http://dx.doi.org/10.25221/fee.471.1 + +journal article +293143 +10.25221/fee.471.1 +3bd3e8b4-a0b1-419c-b415-bbba75cab956 +2713-2196 +7616360 +BD6B6967-8787-4701-A9B5-EBF4CC19F7D3 + + + + + + + +Belyta sanguinolenta +Nees, 1834 + + + + + + + +Figs 35–40 + + + + +MATERIAL EXAMINED ( +86 ♂ +). +Gilan Province +: +Roodsar +, +Rahimabad +, +Ghazichak +( +36°45′52.62″ N +, +50°20′01.08″ E +, + +1787 m +a.s.l. + +), + +03.V 2010 + +, +1 ♂ +( +TMUC +); +Roudsar +, +Rahimabad +, +Orkom +( +36°45′44.34″ N +, +50°18′11.88″ E +, + +1201 m +a.s.l. + +), + +03.V 2010 + +, +1 ♂ +( +TMUC +); + +14.VI 2010 + +, +5 ♂ +( +TMUC +); + +06.VII 2010 + +, +3 ♂ +( +TMUC +); +Astaneh Ashrafiyeh +, +Eshman +kamachal ( +37°22′03.66″ N +, +49°57′57.84″ E +, + +1 m +b.s.l. + +), + +07.VI 2010 + +, +1 ♂ +( +TMUC +); leg.: +M. Khayrandish. Astara +, +Lavandevil forest +( +38°18′19″ N +, +48°42′57″ E +, + +873m +a.s.l. + +), + +06.VI 2017 + +, +1 ♂ +( +TMUC +); + +08.VII 2017 + +, +1 ♂ +, leg. +S. Farahani +( +TMUC +); +Rezvan Shahr +( +37°31′00″ N +, +49°02′07″ E +, + +199 m + +a.s.l), + +13.V 2018 + +, +27 ♂ +( +TMUC +); +Shafaroud forest +( +37°28′18ʺ N +, +48°49′23ʺ E +, + +1114 m + +a.s.l), + +25.VI 2018 + +, +12 ♂ +( +RIRF +). +Mazandaran Province +: +Galanderoud +( +36°26′56″ N +, +51°51′20″ E +, + +1407 m + +a.s.l), + +24.VII 2018 + +, +4 ♂ +( +TMUC +); + +28.VIII 2018 + +, +2 ♂ +( +RIRF +); +Kheyroud Kenar +( +36°34′36.23ʺ N +, +51°34′37.94ʺ E +, + +722 m + +a.s.l), + +24.VII 2018 + +, +8 ♂ +( +TMUC +); + +28.VIII 2018 + +, +1 ♂ +( +TMUC +); +Neka forest +( +36°30′00.4″ N +, +53°27′14.2″ E +, + +828 m + +a.s.l), + +16.V 2017 + +, +4 ♂ +( +TMUC +); +Neka forest +( +36°34′49.2″ N +, +53°27′55.6″ E +, + +465 m + +a.s.l), + +24.VII 2018 + +, +12 ♂ +( +RIRF +). +Golestan Province +: +Shast Kola forest +( +36°44′10.83″ N +, +54°24′11.23″ E +, + +754 m + +a.s.l), + +26.VI 2019 + +, +3 ♂ +( +TMUC +); +Bandar Gaz +, +Nowkandeh +, +Cheshme Bolbol +( +36°41′37.16″ N +, +53°53′07.24″ E +, + +190 m + +a.s.l), + +26.VI 2019 + +, +1♂ +, leg. +F. Kazerani +( +TMUC +). + + + + +DIAGNOSIS: +Male +( +Fig. 35 +). Body length +3.1–3.5 mm +, face smooth and pubescent ( +Fig. 36 +), head in dorsal view transverse, 1.8 times as wide as long, smooth and pubescent ( +Fig. 37 +); POL as long as OOL; antenna slender, A3 basally with emargination, reaching 0.33 of this segment length; A4 3.5 times as long as wide ( +Fig. 38 +); epomia present, moderately prominent; mesoscutum convex and pubescent; anterior scutellar pit semicircular; scutellum convex and bare; fore wing length +2.9–3.2 mm +, marginal vein 0.6–0.75 times as long as its distance from basal vein ( +Fig. 39 +); propodeum pubescent, median propodeal keel simple or forked ( +Fig. 40 +); petiole in dorsal view 1.8–2.1 times as long as wide, with longitudinal keels ( +Fig. 40 +); T2 anteriorly with striations that similar in length. + + + + +DISTRIBUTION: +Iran +(new record); +Czech Republic +, +Finland +, +France +, +Germany +, +Hungary +, +Japan +, +Malta +, +Norway +, +Poland +, +Romania +, +Russia +, +Scotland +, +Sweden +, +Slovakia +, +Switzerland +, +China +( +Taiwan) +, former +Yugoslavia +( +Nixon, 1957 +; +Hellén, 1964 +; +Wall, 1993 +; +Macek, 1996 +; +Notton & Mifsud, 2019 +). + + + + \ No newline at end of file diff --git a/data/38/77/E0/3877E0A39739A1906D6591E7D4B444D0.xml b/data/38/77/E0/3877E0A39739A1906D6591E7D4B444D0.xml new file mode 100644 index 00000000000..13a117e3291 --- /dev/null +++ b/data/38/77/E0/3877E0A39739A1906D6591E7D4B444D0.xml @@ -0,0 +1,124 @@ + + + +Australian gall-inducing scale insects on Eucalyptus: revision of Opisthoscelis Schrader (Coccoidea, Eriococcidae) and descriptions of a new genus and nine new species + + + +Author + +Hardy, Nate B. + + + +Author + +Gullan, Penny J. + +text + + +ZooKeys + + +2010 + +58 + + +1 +74 + + + + +http://dx.doi.org/10.3897/zookeys.58.507 + +journal article +http://dx.doi.org/10.3897/zookeys.58.507 +1313-2970-58-1 + + + + +Opisthoscelis Schrader + + + + +Opisthoscelis +Schrader 1863: 7 +. Type species: +Opisthoscelis subrotunda +Schrader 1863 +, subsequently designated by +Fernald 1903: 46 +. + + +Ophistocelis +; +Signoret 1868: 525 +. Misspelling of genus name + + +Ophiscelis +; +Signoret 1869a: 834 +. Misspelling of genus name. + + +Opliscelis +; +Signoret 1869a: 855, 872 +. Misspelling of genus name. + + +Ophistoscelis +; +Signoret 1869b: 100 +. Misspelling of genus name. + + + +Generic diagnosis. Adult female and associated gall. + +Galls on leaves; each typically globular, conical or hemispherical, rarely pit-like; with small circular, slit-like or fissured orifice/opening often on adaxial (upper) surface, but surface often difficult to determine in mature isobilateral leaves and galls typically opening on same surface on any one leaf. Body outline circular to elliptical; dorsum usually smaller than venter, especially at maturity, with whole of dorsum, a sclerotised part of it, or abdominal apex plugging gall orifice; body of mature female usually tightly fitting gall cavity. Abdomen not tapered. Vulva and anal opening ventral on posterior abdomen, with vulva between abdominal segments VII and VIII. Eyes on margin or dorsad of it. Antennae reduced, with ≤ 7 segments, segmentation often indistinct. Pair of broad frontal lobes posteromedial of antennae. Oral lobes membranous to sclerotic, often forming large circular pad around mouthparts. Tentorial box with aliform anterior extensions. Fore and mid legs varying from well developed to highly reduced, with some segmentation always apparent. Hind legs, on posterior of metathorax, sometimes appearing to be on anterior abdomen, large, always well developed, often elongate; ratio of length of trochanter + femur / length of tibia + tarsus approximately = 1:1; tibia-femur articulation functional; translucent pores present on at least tibia; trochanter with 2 or 3 campaniform sensilla on each side; claw digitules and tarsal digitules either well developed or highly reduced to absent. Anal opening surrounded by anal ring with ≥ 6 (range 6-20) setae; anal ring may be invaginated. Posterior abdominal segments usually with marginal fleshy projections (absent in +Opisthoscelis thurgoona +sp. n. and +Opisthoscelis tuberculata +sp. n.), each projection bearing spines or with a blunt sclerotic point. Marginal fringe of enlarged setae usually present (absent in +Opisthoscelis serrata +). Dorsal setae bristle-like to flagellate, minute to large, 4-148 +µm +long (stout conical setae present in +Opisthoscelis subrotunda +). Cribriform plates or tight clusters of tubular ducts either present or absent on dorsum. Microtubular ducts usually absent (present in +Opisthoscelis ungulifinis +sp. n.). Dorsal quinquelocular pores absent. Venter with macrotubular ducts present or absent; if +present +, with vestibule thin and sclerotic. Quinquelocular pores present on venter, at least around vulva and spiracles. + + +Adult male. +Antenna 10-segmented. Abdomen not elongated. Gland pouches present, each with pair of setae. + + +First-instar nymph. +Anterior margin of head incised at midline. Each spiracle with one trilocular pore next to opening. One submedial longitudinal row of dorsal setae on each side of body. Antennae 4-segmented, with 4 fleshy setae on apical segments. + + +Etymology. + +The genus name is a Latinised combination of the Greek words opisthen, meaning behind, and skelos, meaning leg, and clearly refers to the long hind legs of the adult female because +Schrader (1863: 6) +diagnosed +Opisthoscelis +with one brief statement: "Where they have only two long posterior legs." The name +Opisthoscelis +is treated as feminine. + + + + + \ No newline at end of file diff --git a/data/38/78/0D/38780D2EC5BF16D192A2E9BB9BCD35B1.xml b/data/38/78/0D/38780D2EC5BF16D192A2E9BB9BCD35B1.xml new file mode 100644 index 00000000000..fd2e8f4e1ea --- /dev/null +++ b/data/38/78/0D/38780D2EC5BF16D192A2E9BB9BCD35B1.xml @@ -0,0 +1,111 @@ + + + +Order Primates + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +111 +184 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Lepilemur dorsalis +Gray 1870 + + + + + + + +Lepilemur dorsalis +Gray 1870 + +, +Cat. Monkeys, Lemurs, Fruit-eating Bats Brit. Mus.: 135 + +. + + + + +Type Locality: + +NW +Madagascar +. + + + + + +Vernacular Names: +Black-striped Sportive Lemur +. + + + + +Synonyms: + +Lepilemur grandidieri +(Forsyth Major 1894) + +. + + + + +Distribution: +Nosi Bé, Nosy Komba, and Sambirano region (NW +Madagascar +). + + + + +Conservation: +CITES +– Appendix I; +U.S. +ESA +– Endangered; +IUCN +– Vulnerable. + + + + \ No newline at end of file diff --git a/data/38/78/40/387840149C00C460BAD9FAF58DD4EE3B.xml b/data/38/78/40/387840149C00C460BAD9FAF58DD4EE3B.xml new file mode 100644 index 00000000000..ed74ed2a677 --- /dev/null +++ b/data/38/78/40/387840149C00C460BAD9FAF58DD4EE3B.xml @@ -0,0 +1,52 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828-4-9042 + + + + + +Bioblapsis +Foerster +, 1869 + + + + + +TRICHOMASTIX +Vollenhoven, 1878 + + + + \ No newline at end of file diff --git a/data/38/78/7E/38787E74FF9BE21A9DDCFDD0FEE19765.xml b/data/38/78/7E/38787E74FF9BE21A9DDCFDD0FEE19765.xml new file mode 100644 index 00000000000..6112e28182e --- /dev/null +++ b/data/38/78/7E/38787E74FF9BE21A9DDCFDD0FEE19765.xml @@ -0,0 +1,1535 @@ + + + +Studies of the genus Anthelephila (Coleoptera: Anthicidae) 13. The species described by W. W. Saunders from India + + + +Author + +Kejval, Zbyněk +Muzeum Chodska, Chodské náměstí 96, CZ- 344 01 Domažlice, Czech Republic +anthicid@seznam.cz + +text + + +Acta Entomologica Musei Nationalis Pragae + + +2015 + +2015-06-01 + + +55 + + +1 + + +249 +260 + + + +journal article +20056 +10.5281/zenodo.5319048 +812839c1-fe2e-46fd-843a-6c51c1c5ea94 +0374-1036 +5319048 +5D490866-C8BB-4708-AB3B-422E3D2C4B1EM + + + + + + + +Anthelephila ruficollis +Saunders, 1834 + + + + + + + +( +Figs 8–11 +, +17 +) + + + + + + + +Anthelephila ruficollis +Saunders, 1834: 65 + + +, Pl. 7, +Fig. 8 +; + +SAKAI (1989) +: 412 + +(catalogue); + +LAFER (1996) +: 37 + +(male characters, key, rec. +Japan +, +Vietnam +); + +TELNOV (2001) +: 184 + +(rec. +Indonesia +); + +CHANDLER et al. (2008) +: 423 + +(catalogue, distribution). + + + + + +Anthelephilus ruficollis + +: + +LAFERTÉ- SÉNECTÈRE (1849a) +: 3 + +(redescription, rec. +Myanmar +); + +UHMANN (1983) +: 194 + +(rec. +Vietnam +, +Laos +, +India +), + +UHMANN (1985) +: 125 + +(rec. +Vietnam +), + +UHMANN (1994a) +: 670 + +(rec. +Thailand +, +Vietnam +), + +UHMANN (1994b) +: 409 + +(rec. +Malaysia +), + +UHMANN (1996) +: 27 + +(rec. +Malaysia +, +Thailand +); + +TELNOV (1997) +: 63 + +(distribution, rec. +Vietnam +), + +TELNOV (1998a) +: 87 + +(distribution, rec. +Vietnam +), + +TELNOV (1998b) +: 90 + +(rec. +Indonesia +), + +TELNOV (1999b) +: 76 + +(rec. +Thailand +); + +UHMANN (2000) +: 157 + +(rec. +Malaysia +); + +KEJVAL (2003) +: 382 + +(note). + + + + + +Antelophilus +ruficollis + +(incorrect subsequent spelling): + +PIC (1899b) +: 758 + +(rec. +Indonesia +). + + + + + + +Formicomus ruficollis +: +PIC (1907) + +: 339 + +(rec. +Myanmar +); + +BONADONA (1978) +: 72 + +(rec. +Bangladesh +). + + + + + + +Formicomus ruficollis +var. +annamitus +Pic, 1903a: 56 + + +, + +syn. nov. + + + + + + + +Formicomus uncinatus +Desbrochers, 1875: 42 + + +; + +DESBROCHERS DES LOGES (1881) +: 152 + +(note on identity); + +PIC (1895) +: 19 + +(note on identity, rec. +Syria +); + +PIC (1898) +: 20 + +(note); + +UHMANN et al. (2005) +: 11 + +(note); +syn. nov. + + + + + + +Anthelephila uncinata +: +CHANDLER et al. (2008) + +: 424 + +(catalogue, distribution). + + + + + + +Formicomus +( +Anthelephilus +) +inhumeralis +Pic, 1903b: 644 + + +, + +syn. nov. + + + + + + +Anthelephilus inhumeralis + +: + +KREKICH- STRASSOLDO (1929) +:475 + +(rec. +Philippines +); + +UHMANN (1985) +:127 + +(rec. +Indonesia +), + +UHMANN (1990) +: 583 + +(rec. +Indonesia +), + +UHMANN (1996) +: 27 + +(rec. +Indonesia +). + + + + + + +Anthelephilus cyanochrous +Nomura, 1962: 2 + + +, Pl. 1, + +Figs 3–5. + +NOMURA + + +(1970): 104 (as synonym of + +A. ruficollis + +). + + + + + + +Type +localities. + + +Anthelephila ruficollis + +: +India +, +West Bengal +, +S of Calcutta +, +banks of Hooghly River +. + +Anthelephilus cyanochrous + +: +Japan +, Ryukyu Islands. + +Formicomus +( +Anthelephilus +) +inhumeralis + +: +Philippines +, +Manila +. + +F. ruficollis +var. +annamitus + +: Central +Vietnam +, Phuc-Son. + +F. uncinatus + +: +Syria +. + + +Type material. + + +Anthelephila ruficollis + +: +SYNTYPE +: ♂, ‘W [h] // W. S Saunders East Ind [h; somewhat illegible] // Putative +syntype +Anthelephila ruficollis Saunders, W. W., 1834 Trans Ent Soc. Lon. +1: 65, pl. 7 fig. 8 Removed to type coll. Teste D.J. Mann, +viii.2003 +[p] // TYPE COLE 2138 +Anthelephila ruficollis Saunders, W. W., 1834 HOPE ENT COLL., OUMNH +[p]’ ( +OXUM +). + + + + + +Formicomus ruficollis +var. +annamitus + +: +SYNTYPES +: +1 ♀ +, ‘Annam Phuc-Son Nov. Dez. H. Fruhstorfer [p; black frame] // type [h; yellowish label] // TYPE [p; red label] // +v. annamitus Pic +[h]’ ( +MNHN +) + +; + +2 ♂♂ +2 ♀♀ +, bearing only identical 1st label ( +MNHN +). + + + + + +Formicomus inhumeralis + +: +SYNTYPES +: 1 ♂, ‘ +Manille +Baer +[p] // type [h; yellowish label] // TYPE [p; red label] // +inhumeralis Pic +[h]’ ( +MNHN +); + + +1 ♂, ‘ +Manile’ +[h; partly illegible] ( +MNHN +); + + +1 ♂ +1 ♀ +, ‘ +Manile +[h] // inhumeralis [h]’ ( +MNHN +). + + + +Additional material. + + +AFGHANISTAN +: +KUNDUZ +PROVINCE: + +1 ♀ +, +Kunduz +, +7.vii.1964 +, Nurolhak [lgt.] ( +NMPC +). + + + +BANGLADESH +: +DHAKA +DIVISION: + +1 ♂ +3 ♀♀ +, +Dhaka +, +8.v.–18.ix.1945 +[different dates], D. Leston lgt. ( +BMNH +); + + + +RANGPUR DIVISION + +: 1♂, Dhanjuri,near Dinajpur, +vi.1963 +[no collector] ( +MNHN +, coll.Bonadona); + + + +RAJSHAHI DIVISION + +: 1 ♂, +Rajshahi +, +6.iv.1993 +[no collector] ( +BMNH +); 1♂, Sripur, +viii.–xii.1990 +[no collector] ( +BMNH +). + + + +BHUTAN +: + +1♂, +Samchi +, +300 m +, +7.–11.v.1972 +[no collector, Basel Museum expedition] ( +MNHN +, coll. Bonadona); + + +1 ♂, Gayligphu, +21.viii.1989 +[no collector] ( +BMNH +). + + + +CHINA +: +MACAO + +: +1 ♀ +, Macao, 1906, F. Muir lgt. ( +DCDC +). +GUANGDONG +: 2 ♂♂ +1 ♀ +, Guangzhou [= Canton], +1.–30.x.1916 +, H. Weigold lgt. ( +ZKDC +); + + +1 ♀ +, same locality, +3.x.1963 +[no collector] ( +NMPC +); 1 ♂, same locality, +vi.1983 +, Bouček lgt. ( +BMNH +). + + + +INDIA +: + +1 ♂, Andaman Island, +10 km +of Port Blair, lowland forest, +vi.1991 +, S. Jakl lgt. ( +ZKDC +). + + + +INDONESIA +: +JAVA +: + +2 ♂♂, Batavia, +viii.1947 +and 1949, C. v. Nidek lgt. ( +ZKDC +); 2 ♂♂ +1 ♀ +, +Jakarta +, +6.v.1959 +, B. Pisarski & J. Proszynski lgt. ( +ZKDC +). + + + +EAST JAVA PROVINCE +: + +1 ♂, Sempolan, +400–500 m +, +i.1998 +, local collector ( +ZKDC +). + + + +BALI PROVINCE +: + +1♂, +Bali +, Margarana, +15 km +E of Gilimanuk, +23.ii.1994 +, Bolm lgt. ( +ZKDC +). + + + +CENTRAL JAVA PROVINCE +: + +1♀ +, Pekalongan, +iii.1907 +, F. Muir lgt.( +DCDC +). + + + +EAST NUSA TENGGARA PROVINCE +: + +1♂, Sumba, Tarimbang env., +0–100 m +, +2.–3.ii.2001 +, P.Votruba lgt.( +ZKDC +). + + + +SOUTH SULAWESI PROVINCE +: + +1 ♂, 20.– +35 km +NW of Palopo, +1000–1400 m +, +4.–5.iv.1999 +, Bečvář & J. Zábranský lgt. ( +ZKDC +). + + + +SOUTH EAST +SULAWESI PROVINCE +: + +1 ♂, Buton Island, Wakarumba, +3.–7.ii.1994 +, M. Štrba & I. Jeniš lgt. ( +ZKDC +). + + + +WEST NUSA TENGGARA PROVINCE +: + +2 ♂♂, Lombok, Senaro, N slope of Rinjani, +1100 m +, +2.–5.ii.1994 +, Bolm lgt. ( +ZKDC +). + + + +JAPAN +: + +1 ♂, +Okinawa +, Shimabuku, +20.v.–1.vi.1945 +, C. T. Parsons & F. G. Werner lgt. ( +ZKDC +); + + +3 ♂♂, +Okinawa +, Iwa, +vii.–viii.1945 +, C. T. Parsons & F. G. Werner lgt. ( +ZKDC +). + + + +MALAYSIA +: +JOHOR +: + +1 ♂, Batu Pahat, Baum [lgt., no date] ( +NMPC +); +1 ♀ +, Lombong, +15 km +N of Kota Tinggi, +27.–30.vii.1992 +, R. Schuh lgt. ( +ZKDC +). + + + +KELANTAN +: + +1 ♀ +, +sawmill near Dabong +, +05°18′20′′N +101°59′30′′E +(WGS84), + +23.vii.2001 + +, +R. Fouque & H. Bartlová +lgt. ( +ZKDC +); + + + +PAHANG +: + +2 ♂♂ +1 ♀ +, +Benom Mountains +, + +15 km +E of + +Kampong Dong +, +3°53′N +102°01′E +, + +700 m + +, + +1.iv.1998 + +, +D. Hauck +lgt. ( +ZKDC +); + + +1 ♀ +, Banjaran Benom Mountains, +20 km +S of Kampong Ulu Dong, +1500–1900 m +, +17.–23.iv.1997 +, P. Čechovský lgt. ( +ZKDC +); + + +1 ♂ +10 ♀♀ +, +Tioman Island +, +Kampong Tekek – K. Juara +, +2°48′N +104°11′E +, + +5–295 m + +, + +7.–25.ii.2000 + +, +M. Štrba +lgt. ( +ZKDC +) + +; + +1 ♂ +2 ♀♀ +, same data, except: R. Hergovits lgt. ( +ZKDC +); + + +1 ♂, Raub env., +23.–24.ii.1995 +, M. Štrba & R. Hergovits lgt. ( +ZKDC +); + + + +SABAH +: + +1 ♀ +, Banjaran Crocker Mountains, Gunung Alab Peak, +1650–1800 m +, +30.iv.–27.v.1996 +, M. Štrba & R. Hergovits lgt. ( +ZKDC +). + + + +MYANMAR +: +TANINTHARYI +REGION + +: 4 ♂♂ +8 ♀♀ +, ‘MUSEUM PRAG HINTER-JNDIEN [sic!] Tenasserim // coll. Helfer // ruficollis det. v. Krekich’ ( +NMPC +); 2 ♂♂ +3 ♀♀ +, ‘Ind. or. // Helfer [lgt.]’ ( +NMPC +). + + + +BAGO REGION +: + +1 ♂, Chanthakwin, +ii.1997 +, M. Klícha lgt. ( +ZKDC +). + + + +YANGON REGION +: + +6 ♂♂ +4 ♀♀ +, +Yangon +[= +Rangoon +], +12.–18.i.1981 +, de Rougemont lgt. ( +MNHN +, coll. Bonadona). + + + +NEPAL +: +KOSHI +ZONE: + +1 ♂, Morang Distr., Biratnagar, +140 m +, +21.v.1980 +, C. Holzschuh lgt. ( +ZKDC +). + + + +PHILIPPINES +: + +12 ♂♂ +3 ♀♀ +, Luzon, Los Baños, W. H. Weston lgt. ( +DCDC +, +ZKDC +). + + + +SYRIA +: + +1 ♂ +1 ♀ +, ‘Syria // coll. Lethierry // +Formicomus uncinatus Dsbr. +’ (coll. Pic, +MNHN +). + + + +THAILAND +: +AYUTTHAYA +PROVINCE: + +5 ♀♀ +, +Ayutthaya +, +26.i.1995 +, A. Weigel lgt. ( +NKME +). + + + +CHONBURI PROVINCE +: + +8 ♂♂ +3 ♀♀ +, Pattaya, Jomtien, Pinnacle Resort & Club, KLS, +30.ix.1999 +, M. Hartmann lgt. ( +NKME +). + + + +CHUMPHON PROVINCE +: + +1 ♂ +1 ♀ +, +Pha To env. +, +9°48′N +98°47′E +, + +1.–12.iii.1996 + +, +P. Průdek +lgt. ( +ZKDC +); + + +3 ♂♂ +7 ♀♀ +, same locality, +1.–20.iii.1996 +, K. Majer lgt. ( +ZKDC +); + + +39 ♂♂ +32 ♀♀ +, same locality, +1.–11.v.1998 +, P. Průdek & R. Šigut lgt. ( +ZKDC +). + + + +MAE HONG SON PROVINCE +: + +5 ♂♂ +3 ♀♀ +, Ban Si Lang, +1200 m +, +1.–8.v.1992 +, J. Horák lgt. ( +ZKDC +). + + + +PATTANI PROVINCE +: + +1 ♀ +, Sai Buri, +23.–28.iv.1993 +, J. Horák lgt. ( +ZKDC +); +1 ♀ +, Gappoa Panat Nikhom, +3.xi.1981 +, G. A. Shook lgt. ( +ZKDC +). + + + +RANONG PROVINCE +: + +7 ♂♂ +3 ♀♀ +, +Ban Na env. +, +9°34′N +98°42′E +, + +22.–26.iii.1996 + +, +K. Majer +lgt. ( +ZKDC +). + + + +RAYONG PROVINCE +: + +2 ♂♂ +1 ♀ +, +5 km +W of +Rayong +Centre, +27.ix.1999 +, M. Hartmann lgt. ( +NKME +); + + +2 ♀♀ +, +Rayong Prov. +, Klaeng, +21.i.1995 +, A. Weigel lgt. ( +NKME +). + + + +TRAT PROVINCE +: + +1 ♂ +2 ♀♀ +, Ko Chang Island, +25.–31.v.2003 +, O. Šafránek lgt. ( +ZKDC +). + + + +YALA PROVINCE +: + +3 ♂♂ +2 ♀♀ +, Betong, +23.–25.iv.1992 +, J. Horák lgt. ( +ZKDC +); + + +2 ♂♂ +3 ♀♀ +, Betong, Guning Cang dun vill., +25.iii.–22. iv.1993 +, J. Horák lgt. ( +ZKDC +). + + + +VIETNAM +: +DA +NANG PROVINCE: + +5 ♀♀ +, +Da Nang +, Red Beach, +2.–3.xi.1970 +, A. R. Gillogly lgt. ( +ZKDC +, +ZSMC +). + + + +HA NOI PROVINCE +: + +2 ♂♂ +2 ♀♀ +, +Hanoi +, +3.v.1966 +, R. Bielawski & B. Pisarski lgt. ( +ZKDC +, +ZSMC +); + + +1 ♂ +1 ♀ +, +Hanoi +, Hotel Kim-lien, +1.–2.v.1966 +, G. Topál lgt. ( +ZKDC +); + + +1 ♀ +, Mai lam, NE of +Hanoi +, +12.–14.iv.1966 +, G. Topál lgt. ( +ZKDC +); + + +1 ♀ +, Phuc-Son [no date], Fruhstorfer lgt. ( +ZKDC +). + + + +HA NAM PROVINCE +: + +2 ♂♂ +2 ♀♀ +, Tuong linh, near Phu ly, +19.–23.v.1966 +, G. Topál lgt. ( +ZKDC +, +ZSMC +). + + + +HA TINH PROVINCE +: + +2 ♂♂ +3 ♀♀ +, +Ky Thuong +, +18°01’N +106°08’E +, + +100 m + +, + +vii.1997 + +, +T. Ziegler +lgt. ( +ZKDC +, +ZSMC +). + + + + + +Redescription +(male, Biratnagar, ZKDC). Body length +4.2 mm +. Head black, pronotum dark reddish, elytra black; antennae and legs black, base of femora reddish. + +Head 1.2 times as long as wide, including eyes; base rather widely rounded, its outline moderately convex medially in dorsal view, tempora moderately narrowing posteriorly, posterior temporal angles indistinct. Eyes small, moderately convex. Surface glossy, distinctly punctate dorsally; punctures mostly dense but well-spaced, distinctly sparser near base. Setation short, decumbent, with scattered long, erect tactile setae.Antennae moderately long, distinctly enlarged in distal third; antennomere X 1.5 times, XI 2.5 times as long as wide. +Pronotum robust, 1.4 times as long as wide, slightly narrower than head including eyes, nearly evenly rounded anteriorly, distinctly impressed laterally in posterior half; pronotal disc evenly shaped, its outline nearly evenly convex in lateral view. Surface glossy, distinctly punctate; punctures unevenly spaced, pronotal disc somewhat sparsely punctured postero-medially (glossy, unwrinkled), and dorso-laterally in posterior half with paired longitudinal strip of fine wrinkles and dense punctures; lateral surface largely impunctate and glossy, including latero-basal impressions. Setation similar to that of head, subdecumbent, with scattered long tactile setae. +Meso- and metaventrite simple. +Elytra 1.7 times as long as wide, convex, subtruncate apically; humeri slightly marked, omoplates and postbasal impression absent. Surface distinctly and rather evenly punctate, glossy. Setation conspicuous, mostly decumbent to suberect, with numerous, moderately longer erect tactile setae. +Legs robust; profemora with strong lobe-like process; protibiae with distinct, blunt protrusion in distal half; penultimate tarsomere widened and flattened distally, with terminal tarsomere articulated dorsally in all tarsi. + +Abdominal characters as in +Figs 9–13 +; prongs of sternite VIII lobed dorso-medially at about mid-length and densely setose medially and ventrally; apical portion of tegmen 0.6 times as long as basal piece. + + +Variation. +Body length +3.2–4.6 mm +. Pronotum usually reddish ( +Fig. 17 +), sometimes more or less darkened anteriorly (SE Asia). Specimens from the +Philippines +and +Indonesia +are nearly entirely black. The base of the head more or less evenly rounded. + +Female sternum VII simple, slightly produced postero-medially; female tergum VII subtriangular, rounded apically. + + + +Differential diagnosis. + +Anthelephila ruficollis + +resembles + +A. limaria +Kejval, 2006 + +from +Nepal +and Northern +India +in body form and colouration, but differs in lack of a distinct bluish reflection of the elytra, the semicircular to somewhat widely rounded head base, the simple mesoventrite (lacking any median edge and /or protrusion in both sexes), and the apically simply-rounded female tergum VII (strongly narrowed, with obtuse to slightly incised apex in + +A. limaria + +). Male characters of these two species are quite dissimilar. + + + + +Distribution. +Afghanistan +, +Bangladesh +, +Bhutan +, +China +(SE provinces), +India +( +West Bengal +, Andaman Islands), +Indonesia +( +Bali +, Lombok, +Java +, +Sumatra +, Sumba, +Sulawesi +), +Japan +, +Laos +, +Malaysia +, +Myanmar +, +Nepal +, +Philippines +, +Syria +, +Thailand +, +Vietnam +. + + + + +Remarks. +PIC (1903a +,b) described + +Formicomus ruficollis +var. +annamitus + +from +Vietnam +and + +Formicomus +( +Anthelephilus +) +inhumeralis + +from the +Philippines +(Luzon). Having examined the relevant +types +and numerous additional specimens from SE Asia, including the +Philippines +and +Indonesia +, I failed to find any substantial differences in male characters from + +Anthelephila ruficollis + +. Consequently both taxa are regarded as junior synonyms of this species. + + +DESBROCHERS DES LOGES (1881) +described + +Formicomus uncinatus + +from an unstated number of specimens originating from +Syria +. This species is known only from +Syria +( +PIC 1895 +, +1898 +; +CHANDLER et al. 2008 +), and its +type +material has never been examined. I failed to find any +type +specimens in MNHN and other major collections; nevertheless, the original description comprises several remarkable morphological characters revealing, in my opinion, its species identity: elytral humeri absent (‘épaules nulles’), elytral apices truncate (‘sommet des élytres largement trongué’), and male profemoral process robust and apically hooked (‘une trés-grande dent terminée par un crochet’). Combination of these three characters is rarely present within the genus; however, they are all shared by + +Anthelephila ruficollis + +, including the very similar colouration. Moreover, the record of + +F. uncinatus + +from +Syria +by +PIC (1895) +was found to be based on specimens of + +A. ruficollis + +, therefore + +F. uncinatus + +is regarded as a junior synonym of the latter species. + + + +Figs 8–13. + +Anthelephila ruficollis +Saunders, 1834 + +(Biratnagar, male): 8 – profemur and protibia; 9 – sternum VII; 10 – tergum VII; 11 – sternite VIII (half) in dorsal view; 12 – tergite VIII; 13 – apical portion of aedeagus. Scales (0.5 mm): A – Fig. 13; B – Fig. 11; C – Figs 8, 9, 12; D – Fig. 10. + + + + +Figs 14–17. Body in dorsal view. 14 – + +Anthelephila mutillaria +Saunders, 1834 + +(male), Chitwan NP; 15 – same species (male), Soppong; 16 – same species (female), Yuanxian; 17 – + +A. ruficollis +Saunders, 1834 + +(male), Betong. + + + +As already stated by LAFERTÉ- SÉNECTÈRE (1849a), + +Anthelephila bengalensis +(Wiedemann, 1823) + +is very probably conspecific with + +A. ruficollis + +. It was described from the same region, probably +Bangladesh +(‘Bengalia’), and later recorded from +Japan +and +Vietnam +( +MARSEUL 1876 +; +UHMANN 1983 +, +1985 +; +CHANDLER et al. 2008 +). At least some of the Uhmann’s records of + +A. bengalensis + +from +Vietnam +( +UHMANN 1983 +) surely belong to this species. + + + +Anthelephila ruficollis + +appears to be common and widespread species. Based on label data, part of the examined specimens were collected on beaches, from a rat carcass, by sifting litter, by treading mud next to water, or by means of attraction to cantharidin bait ( +Thailand +, G. A. Shook lgt.). + + + + \ No newline at end of file diff --git a/data/38/78/7E/38787E74FF9FE2159D26FB83FB989425.xml b/data/38/78/7E/38787E74FF9FE2159D26FB83FB989425.xml new file mode 100644 index 00000000000..80289aae2b8 --- /dev/null +++ b/data/38/78/7E/38787E74FF9FE2159D26FB83FB989425.xml @@ -0,0 +1,994 @@ + + + +Studies of the genus Anthelephila (Coleoptera: Anthicidae) 13. The species described by W. W. Saunders from India + + + +Author + +Kejval, Zbyněk +Muzeum Chodska, Chodské náměstí 96, CZ- 344 01 Domažlice, Czech Republic +anthicid@seznam.cz + +text + + +Acta Entomologica Musei Nationalis Pragae + + +2015 + +2015-06-01 + + +55 + + +1 + + +249 +260 + + + +journal article +20056 +10.5281/zenodo.5319048 +812839c1-fe2e-46fd-843a-6c51c1c5ea94 +0374-1036 +5319048 +5D490866-C8BB-4708-AB3B-422E3D2C4B1EM + + + + + + + +Anthelephila mutillaria +Saunders, 1834 + + + + + + + +( +Figs 1–7 +, +14–16 +) + + + + + + + +Anthelephila mutillaria +Saunders, 1834: 66 + + +, Pl. 7, +Fig. 9 +: + +CHANDLER et al. (2008) +: 423 + +(catalogue, distribution). + + + +Formicomus mutillarius + +: + +LAFERTÉ- SÉNECTÈRE (1849b) +: 3 + +(redescription, rec. +Myanmar +); + +PIC (1907) +: 339 + +(rec. +Myanmar +); + +BONADONA (1978) +: 72 + +(rec. +Bangladesh +). + + + + +Formicomus mutillarius +var. +tonkineus +Pic, 1899a: 105 + + +, + +syn. nov. + + + + + +Formicomus mutillarius +var. +inapicalis +Pic, 1899a: 106 + + +, + +syn. nov. + + + + + +Formicomus mutillarius +var. +innotatipennis +Pic, 1913: 155 + + +, + +syn. nov. + + + + + +Hirticomus fascifer +Uhmann, 1983: 200 + + +, Fig. 33, +syn. nov. + + + + +Formicomus fascifer +: +TELNOV (1999a) + +: 64 + +, +Figs 1–5 +(new comb., redescription, rec. +Vietnam +). + + + + +Anthelephila fascifer +: +TELNOV (2003) + +: 293 + +(rec. +Nepal +). + + + + + + +Type +localities. + + + +Anthelephila mutillaria + + +: +India +, +West Bengal +, +S of Calcutta +, +banks of Hooghly River +. + + +Formicomus mutillarius tonkineus + + +: +Northern Vietnam +(‘Tonkin’). + +Formicomus mutillarius inapicalis + +: ‘ +India +Orientalis’ [probably southern +Myanmar +, +Tanintharyi Region +]. + + +Formicomus mutillarius innotatipennis + + +: ‘Indes Orientales: +?Tenasserim’ [probably southern Myanmar +, +Tanintharyi Region +]. + +Hirticomus fascifer + +: +Vietnam +, ‘River Chay’ [probably in the +Hà Giang Province +]. + + +Type material. + + + +Anthelephila mutillaria + + +: +SYNTYPE +: + +, ‘Anthel: + +mutillaria +W.W.S. Bengal + +[h] // Coll.(1830-73) W W Saunders Wx coll. H. E. Cox. dd. 1916 Mrs Cox [p] // Syntype +Anthelephila mutillaria Saunders, W. W., 1834 Trans Ent Soc. Lon. +1: 66, pl. 7 fig. 9 teste. D.J. Mann, +viii.2003 +[p] // TYPE COLE 2137 +Anthelephila mutillaria Saunders, W. W., 1834 HOPE ENT COLL., OUMNH +[p]’ ( +OXUM +). + + + + + +Formicomus mutillarius +var. +innotatipennis + +: +SYNTYPE +: + +, ‘Museum +Prag +, Hinter-Jndien, Tenasserim? [sic!; p] // +Coll. Helfer +[p] // type [h] // TYPE [p, red label] // [female symbol]’ (coll. +Pic +, +MNHN +). + + + + + +Formicomus mutillarius +var. +tonkineus + +: +SYNTYPE +: + +, bearing red, printed ‘TYPE’ label (coll. Pic, +MNHN +). + + + +Additional material. + + +BANGLADESH +: +RANGPUR +DIVISION: + +1 ♂, +Dinajpur +, + +x.1969 + +, +Barbe +lgt. ( +MNHN +, coll. +Bonadona +) + +. + + +CHINA +: +YUNNAN +: + +1 ♂ +6 ♀♀ +, + +5 km +NE Yuanxian + +, +24°27′45.1′′N +100°10′37.8′′E +, + +1053 m + +, sandy river bank, flood debris, + +12.ix.2009 + +, +D. W. Wrase +lgt. ( +ZKDC +) + +. + + +INDIA +: +ANDHRA +PRADESH: + +2 ♂♂ +3 ♀♀ +, + +35 km +SE of Rajahmundry + +, +Kottipale +, bank of +Godavari River +, + +23.–24.ii.1994 + +, Z. +Kejval +lgt. ( +ZKDC +) + +. + + +ASSAM +: + +1 ♀ +, +Haflong Hills +, + +18.–25.v.1991 + +, S. +Jakl +lgt. ( +ZKDC +) + +. + + +ORISSA +: + +3 ♂♂ +5 ♀♀ +, + +30 km +NE of Balasore + +, +Jaleswar +env., bank of river, + +13.ii.1994 + +, Z. +Kejval +lgt. ( +ZKDC +) + +. + + +UTTARAKHAND +: + +1 ♂, +Rishikesh +, + +450 m + +, + +viii.1988 + +, +Werner +lgt. ( +ZKDC +) + +. + + +LAOS +: + +1 ♀ +, +Vientiane +city, +17°57′N +102°36′E +, +shore of Mekong +, + +160 m + +, + +4.v.2009 + +, +M. Geiser +lgt. ( +NHMB +). + + + +MYANMAR +: + +2 ♀♀ +, ‘ +Ind. +or. // +Helfer +[lgt.]’ ( +NMPC +). + + + +BAGO REGION + +: 1♂, +Toungoo +, + +29.–31.v.2003 + +, +M. Klícha +lgt. ( +ZKDC +). + + + +YANGON REGION +: + +1 ♂ +2 ♀♀ +, +Hlegu-Goygon +, + +iv.1997 + +, +M. Klícha +lgt. ( +ZKDC +) + +. + + +NEPAL +: +BHERI +ZONE: + +1 ♀ +, ca. + +10 km +E of Nepalganj + +, banks of +Rapti +River +, +28°03′43′′N +81°43′14′′E +, + +120 m + +, + +12.vi.2009 + +, +A. Kopetz +lgt. ( +ZKDC +). + + + +JANAKPUR ZONE +: + +1 ♀ +, Tamba-Koshi-Khola, +SE Charikot +, + +900–1200 m + +, + +5.–10.vi.1987 + +, C. +Holzschuh +lgt. ( +ZKDC +) + +; + +1 ♀ +, +Pokhara +, + +3.vi.1992 + +, I. +Jeniš +lgt. ( +ZKDC +) + +; + +1 ♂ +3 ♀♀ +, +Annapurna Pokhara +, +Phewa river ++ lake, + +800–850 m + +, + +14.–15. ix.2003 + +, J. +Schmidt +lgt. ( +NKME +). + + + +NARAYANI ZONE +: + +3 ♂♂, Sauraha-Thati-Bagh +Mara +, + +17.–21.v.1996 + +, P. +Čechovský +lgt. ( +ZKDC +) + +; + +1 ♂, Sauraha-Thati-Bagh +Mara +, +Chitwan National Park +, + +200–500 m + +, + +2.–3.v.2000 + +, J. & J. +Dalihod +lgt. ( +ZKDC +) + +; + +2 ♀♀ +, same locality, + +4.–6.vi.1999 + +, P. +Kresl +lgt. ( +ZKDC +) + +; + +1 ♂, +Sauraha +, +Chitwan Nat. Park +, at light, + +3.–6.vi.1983 + +[no collector] ( +BMNH +). + + + +RAPTI ZONE +: + +1 ♀ +, + +2 km +S of Lamahi + +, +Rapati River +, +27°50′07′′N +82°32′23′′E +, riverbank + fields, + +13.vii.2001 + +, +A. Kopetz +lgt. ( +NKME +) + +. + + +PAKISTAN +: +KHYBER +PAKHTUNKHWA PROVINCE + +: 1 ♂, + +80 km +E of Peshavar + +, +Indus River valley +, + +viii.2005 + +[no collector] ( +ZKDC +) + +. + + +THAILAND +: +MAE +HONG SON PROVINCE: + +9 ♂♂ +10 ♀♀ +, +Soppong +env., + +600 m + +, + +28.v.–2.vi.1999 + +, M. +Říha +lgt. ( +ZKDC +) + +. + + +VIETNAM +: +HA +NOI PROVINCE: + +1 ♂ +3 ♀♀ +, +Hanoi +, + +15.iv.1918 + +, +Jeanvoine +[lgt.] ( +MNHN +). + + + + + +Redescription +(male, Kottipale, ZKDC). Body length +5.2 mm +. Head black, pronotum dark reddish to red, elytra largely black with reddish basal third; legs black, basal portion of femora reddish, antennae black, basal antennomeres with reddish tinge. + +Head 1.1 times as long as wide, including eyes; base rather widely rounded, its outline moderately convex medially in dorsal view, tempora moderately narrowing posteriorly, posterior temporal angles rounded but distinct. Eyes medium-sized, strongly convex. Surface distinctly and rather evenly punctured dorsally; punctures conspicuously large, shallow, mostly rounded and narrowly spaced, at places (postero-laterally) contiguous, angular and forming cell-like sculpture. Setation conspicuous, with shorter, suberect and numerous longer erect bristly setae.Antennae moderately long, at most slightly enlarged in distal third; antennomere X 2.1 times, XI 2.9 times as long as wide. +Pronotum robust, 1.3 times as long as wide, moderately narrower than head including eyes, somewhat unevenly rounded anteriorly, only moderately impressed laterally in posterior half; pronotal disc evenly shaped, its outline rather evenly convex in lateral view. Surface very distinctly punctate, including lateral sides (finer and sparser only near procoxal cavities); punctures on pronotal disc somewhat smaller and mostly distinctly sparser than those on head, somewhat unevenly spaced; latero-basal impressions unwrinkled. Setation as on head, with numerous long bristly tactile setae. +Mesoventrite with moderately convex, laterally sharply delimited median bulge; metaventrite simple. +Elytra 1.8 times as long as wide, conjointly rounded apically; humeri moderately protruding, omoplates and postbasal impression slightly indicated. Surface distinctly punctate; basal half punctures much smaller and largely sparser than those of head and pronotal disc, dot-like, somewhat unevenly spaced, slightly sparser in basal third, with 2–3 small paired patches of dense punctures near borderline of reddish basal and black middle third. Setation conspicuous, dense and coarse, mostly suberect, with numerous longer erect setae; setae mostly dark coloured, blackish, with contrastingly whitish setae scattered latero-basally, especially on humeri, and forming two transverse bands, anterior band narrow and somewhat uneven (nearly subdecumbent setae originating from patches of dense punctures), posterior band much wider and sparser, situated in apical third. + +Legs rather robust, conspicuously setose, with numerous long erect setae (especially on tibiae); profemora nearly simple, with slight edge on inner side; protibiae enlarged at mid-length and with smooth, moderately projecting lobe in distal half ( +Fig. 1 +); penultimate tarsomere widened / flattened distally, with terminal tarsomere dorsally articulated in all tarsi. + + +Abdominal characters as in +Figs 2–7 +; sternum VIII shallowly impressed medially, its median process simple, curved, projecting from dorsal side close before margin of sternum; tergum VII with conspicuous apical notch; prongs of sternite VIII somewhat laterally flattened, each with two lobes dorsally near base, small ventral process, and two lobules on inner side of apical widened portion, margins of prongs medially with dense short, stiff setation; paired sclerites of tergite VIII with narrow median connection; aedeagus with apical portion of tegmen 0.4 times as long as basal piece. + + +Variation. +Body length +3.7–5.2 mm +. Most specimens from +Nepal +, +Vietnam +and Yunnan with both, basal and apical, thirds of the elytra reddish (typical form, +Fig. 14 +); most specimens from +Myanmar +and +Thailand +(Soppong) with elytra largely or entirely black ( +Fig. 15 +); a specimen from Yunnan generally dark coloured, including brown black pronotum ( +Fig. 16 +). Base of the head in specimens from the Southeast Asia nearly evenly rounded, with indistinct posterior temporal angles and eyes somewhat less convex. The ventral process of prongs in males always well- developed, but less protruding in the specimen from +Vietnam +. + +Female sternum VII simple, moderately produced postero-medially and rounded apically; female tergum VII nearly triangular, rounded apically. + + + +Differential diagnosis. + +Anthelephila mutillaria + +is a very conspicuous, robust species, which can be easily recognized by the following combination of external characters: head and pronotum very coarsely punctate, body setation conspicuous, long and erect (including legs), elytra with setose bands. It differs clearly from all Oriental species in the morphology of male sternite VIII. + + + + +Distribution. +Bangladesh +, +China +( +Yunnan +), +India +( +Andhra Pradesh +, +Assam +, +Orissa +, +Uttarakhand +, +West Bengal +), +Laos +, +Myanmar +, +Nepal +, +Pakistan +, +Thailand +, +Vietnam +. New species to +Pakistan +. + + + + +Remarks. + +Anthelephila mutillaria + +varies considerably in colouration and thus +PIC (1899a +, +1913 +a) described: + +var. +tonkineus + +from northern +Vietnam +(body entirely dark, including pronotum), + +var. +inapicalis + +from +Myanmar +(elytra black, with reddish basal third / fourth, pronotum reddish), and + +var. +innotatipennis + +from +Myanmar +(elytra entirely black, pronotum reddish). In the case of the + +variety +inapicalis +, +PIC (1899a) + +just named ‘var. β’ of + +Formicomus mutillarius + +that had been decribed by LAFERTÉ (1849b). Its +type +material is thus of the same origin as that of + +var. +innotatipennis + +– probably southern +Myanmar +, +Tanintharyi Region +(formerly Tenasserim), from the collection of J. V. Helfer. + + + +Figs 1–7. + +Anthelephila mutillaria +Saunders, 1834 + +(Kottipale, male): 1 – profemur and protibia; 2 – sternum VII; 3 – tergum VII; 4 – sternite VIII (half) in dorsal view; 5 – prong of sternite VIII in lateral view; 6 – tergite VIII; 7 – apical portion of aedeagus. Scales (0.5 mm): A – Fig. 2; B – Figs 4, 5; C – Figs 1, 6; D – Fig. 3; E – Fig. 7. + + + +Although darker specimens of + +A. mutillaria + +are known only from the southern part of its range, they do not seem to be confined to any particular geographical region and may occur together with typically coloured specimens (series from Soppong and Yuanxian). The newly proposed synonymy is based mainly on the examination of male characters that were found rather stable (including setation and the finer structures of sternite VIII) within the examined material. + + +UHMANN (1983) +described + +Hirticomus fascifer + +from a single female specimen collected in northern +Vietnam +(‘River Chay’ probably +Hà Giang Province +). +TELNOV (1999) +examined the +holotype +, proposed the new combination and provided a redescription as + +Formicomus fascifer + +, based on an additional male specimen from +Hanoi +. The male characters presented by +TELNOV (1999) +fully agree with those of + +A. mutillaria + +. The newly proposed synonymy is further confirmed by examination of another male specimen from +Vietnam +(listed above). + + + + \ No newline at end of file diff --git a/data/38/78/85/387885D0DB1362060B02B4D28EB7F89F.xml b/data/38/78/85/387885D0DB1362060B02B4D28EB7F89F.xml new file mode 100644 index 00000000000..ef43d36f421 --- /dev/null +++ b/data/38/78/85/387885D0DB1362060B02B4D28EB7F89F.xml @@ -0,0 +1,265 @@ + + + +Annelids of the eastern Australian abyss collected by the 2017 RV ' Investigator' voyage + + + +Author + +Gunton, Laetitia M. +Australian Museum Research Institute, Sydney, Australia +laetitia.gunton@austmus.gov.au + + + +Author + +Kupriyanova, Elena K. +Australian Museum Research Institute, Sydney, Australia & Macquarie University, Sydney, Australia + + + +Author + +Alvestad, Tom +Department of Natural History, University Museum of Bergen, University of Bergen, Bergen, Norway + + + +Author + +Avery, Lynda +Museums Victoria, Melbourne, Australia + + + +Author + +Blake, James A. +https://orcid.org/0000-0001-8217-9769 +Aquatic Research & Consulting, Duxbury, Massachusetts, USA + + + +Author + +Biriukova, Olga +Museum and Art Gallery of the Northern Territory, Darwin, Australia + + + +Author + +Boeggemann, Markus +University of Vechta, Vechta, Germany + + + +Author + +Borisova, Polina +P. P. Shirshov Institute of Oceanology, Russian Academy of Sciences, Moscow, Russia + + + +Author + +Budaeva, Nataliya +Department of Natural History, University Museum of Bergen, University of Bergen, Bergen, Norway & P. P. Shirshov Institute of Oceanology, Russian Academy of Sciences, Moscow, Russia + + + +Author + +Burghardt, Ingo +Australian Museum Research Institute, Sydney, Australia + + + +Author + +Capa, Maria +https://orcid.org/0000-0002-5063-7961 +Department of Biology, University of the Balearic Islands, Palma, Spain + + + +Author + +Georgieva, Magdalena N. +Natural History Museum, London, UK + + + +Author + +Glasby, Christopher J. +https://orcid.org/0000-0002-9464-1938 +Museum and Art Gallery of the Northern Territory, Darwin, Australia + + + +Author + +Hsueh, Pan-Wen +Department of Life Sciences, National Chung Hsing University, Taichung City, China + + + +Author + +Hutchings, Pat +Australian Museum Research Institute, Sydney, Australia & Macquarie University, Sydney, Australia + + + +Author + +Jimi, Naoto +https://orcid.org/0000-0001-8586-3320 +National Institute of Polar Research, Tachikawa, Tokyo, Japan + + + +Author + +Kongsrud, Jon A. +Department of Natural History, University Museum of Bergen, University of Bergen, Bergen, Norway + + + +Author + +Langeneck, Joachim +https://orcid.org/0000-0003-3665-8683 +Department of Biology, University of Pisa, Pisa, Italy + + + +Author + +Meissner, Karin +Forschungsinstitut Senckenberg, DZMB, Hamburg, Germany + + + +Author + +Murray, Anna +https://orcid.org/0000-0002-1765-1286 +Australian Museum Research Institute, Sydney, Australia + + + +Author + +Nikolic, Mark +Museums Victoria, Melbourne, Australia + + + +Author + +Paxton, Hannelore +https://orcid.org/0000-0001-7086-5219 +Australian Museum Research Institute, Sydney, Australia & Macquarie University, Sydney, Australia + + + +Author + +Ramos, Dino +https://orcid.org/0000-0002-4069-5383 +Natural History Museum, London, UK + + + +Author + +Schulze, Anja +Texas A & M University at Galveston, Galveston, TX, USA + + + +Author + +Sobczyk, Robert +Department of Zoology of Invertebrates and Hydrobiology, University of Lodz, Lodz, Poland + + + +Author + +Watson, Charlotte +Museum and Art Gallery of the Northern Territory, Darwin, Australia + + + +Author + +Wiklund, Helena +Natural History Museum, London, UK & Gothenburg Global Biodiversity Centre and University of Gothenburg, Gothenburg, Sweden + + + +Author + +Wilson, Robin S. +https://orcid.org/0000-0002-9441-2131 +Museums Victoria, Melbourne, Australia + + + +Author + +Zhadan, Anna +Biological Faculty, Lomonosov Moscow State University, Moscow, Russia + + + +Author + +Zhang, Jinghuai +South China Sea Environmental Monitoring Centre, State Oceanic Administration, Guangzhou, China + +text + + +ZooKeys + + +2021 + +2021-02-24 + + +1020 + + +1 +198 + + + + +http://dx.doi.org/10.3897/zookeys.1020.57921 + +journal article +http://dx.doi.org/10.3897/zookeys.1020.57921 +1313-2970-1020-1 +CC23B8CE8C8E473CBD8C44E74252A33D +F6561609F0F15EE8907C94528CA44E4F + + + + +Pseudoscalibregma sp. nov. 1 + + + +Records. +5 specimens. Suppl. material 1: ops. 11, 54, 76 (AM). + + + \ No newline at end of file diff --git a/data/38/78/87/387887D2FFB89248FF26EB53FE05B628.xml b/data/38/78/87/387887D2FFB89248FF26EB53FE05B628.xml new file mode 100644 index 00000000000..a09f741e3c2 --- /dev/null +++ b/data/38/78/87/387887D2FFB89248FF26EB53FE05B628.xml @@ -0,0 +1,145 @@ + + + +Oloughlinia, a replacement name for Clarkiella Heding in Heding & Panning 1954 (Echinodermata: Holothuroidea: Sclerodactylidae) + + + +Author + +Kroh, Andreas +Naturhistorisches Museum Wien, Burgring 7, 1010 Vienna, Austria. + + + +Author + +Gaudin, Jimmy +34, avenue Antoine de Saint-Exupéry 17000, La Rochelle, France. + + + +Author + +Reich, Mike +Staatliches Naturhistorisches Museum, Gaussstrasse 22, 38106 Braunschweig, Germany. & Ludwig-Maximilians-Universität München, Department für Geo- und Umweltwissenschaften, Richard-Wagner-Str. 10, 80333 Munich, Germany. & GeoBio-Center, Richard-Wagner-Str. 10, 80333 Munich, Germany. + +text + + +Zootaxa + + +2022 + +2022-08-29 + + +5178 + + +4 + + +397 +399 + + + +journal article +133167 +10.11646/zootaxa.5178.4.6 +532e7783-a9f8-4280-bb47-167cf7226ac0 +1175-5326 +7031833 +9F797DAC-061C-463F-A75D-10E3A4A9DF78 + + + + + + +Order + +Dendrochirotida +Grube, 1840 + + + + + + + + +Family + +Sclerodactylidae +Panning, 1949 + + + + + +Subfamily + +Cladolabinae +Heding & Panning, 1954 + + + + + + +Remarks: +The assignment of the genus + +Oloughlinia + +(nom. nov. pro + +Clarkiella +Heding + +in +Heding & Panning, 1954 +) to the family +Sclerodactylidae +( +vs. +Cucumariidae +vs. +Cladolabidae) is under discussion (cf. +O’Loughlin 2009 +, pp. 4–6; + +O’Loughlin +et al +. 2011 + +, p. 267; +Smirnov 2012 +, p. 820), especially since the +Sclerodactylidae +and +Cucumariidae +are evidently polyphyletic (e.g. + +Miller +et al +. 2017 + +, fig. 4). +Martins & Tavares (2022 +, p. 569), based on a re-examination of the type-material at ZMUC and +holotype +slides at the MNHN listed + +Clarkiella + +as member of the Subfamily +Cladolabinae +, which is followed here. + + + + \ No newline at end of file diff --git a/data/38/78/87/387887D2FFB99248FF26ED7CFA8EB372.xml b/data/38/78/87/387887D2FFB99248FF26ED7CFA8EB372.xml new file mode 100644 index 00000000000..4431399181a --- /dev/null +++ b/data/38/78/87/387887D2FFB99248FF26ED7CFA8EB372.xml @@ -0,0 +1,221 @@ + + + +Oloughlinia, a replacement name for Clarkiella Heding in Heding & Panning 1954 (Echinodermata: Holothuroidea: Sclerodactylidae) + + + +Author + +Kroh, Andreas +Naturhistorisches Museum Wien, Burgring 7, 1010 Vienna, Austria. + + + +Author + +Gaudin, Jimmy +34, avenue Antoine de Saint-Exupéry 17000, La Rochelle, France. + + + +Author + +Reich, Mike +Staatliches Naturhistorisches Museum, Gaussstrasse 22, 38106 Braunschweig, Germany. & Ludwig-Maximilians-Universität München, Department für Geo- und Umweltwissenschaften, Richard-Wagner-Str. 10, 80333 Munich, Germany. & GeoBio-Center, Richard-Wagner-Str. 10, 80333 Munich, Germany. + +text + + +Zootaxa + + +2022 + +2022-08-29 + + +5178 + + +4 + + +397 +399 + + + +journal article +133167 +10.11646/zootaxa.5178.4.6 +532e7783-a9f8-4280-bb47-167cf7226ac0 +1175-5326 +7031833 +9F797DAC-061C-463F-A75D-10E3A4A9DF78 + + + + + + +Genus + +Oloughlinia +Kroh, Gaudin & Reich, 2022 + +nom. nov. + + + + + + += homonym + +Clarkiella +Heding + +in +Heding & Panning, 1954 +non +Lambert, 1916 + + + + +(pro + +Clarkiella +Heding + +in +Heding & Panning, 1954 +, p. 119, non +Lambert, 1916 +, p. 169 [ +Echinoidea +: +Faujasiidae +]) + +Synonymy: + +non 1916 + +Clarkiella + +—Lambert, p. 169. + + +non 1953 Genus + +Clarkiella +Lambert + +—Cooke, p. 18. + + +1954 Gattung + +Clarkiella +Heding + +—Heding & Panning, p. 119. + + +1956 + +Clarkiella + +gen. nov. +… Heding & Panning—Clark, p. 13. + + + + +1966 + +Clarkiella +Heding & Panning 1954 + +—Edwards & Hopwood, p. 58. + + +2017 + +Clarkiella + +—Martins, p. 18. + + + + +2022 Genus + +Clarkiella +Heding + +, in +Heding & Panning, 1954 +—Martins & Tavares, p. 569. + + + + + +Type +species: + + +Clarkiella discoveryi +Heding + +in +Heding & Panning, 1954 +, pp. 119–120 is designated as +type +species of + +Oloughlinia +Kroh, Gaudin & Reich, 2022 + +nom. nov. here, following recommendation 60A of +the Code +. + +Gender: feminine + + + +Etymology: +named after Peter Mark O’Loughlin (Museum Victoria), in acknowledgement of his extensive research on dendrochirote sea cucumbers. + + + +Species + +Oloughlinia deichmannae +( +O’Loughlin, 2009 +) + +nov. comb. + +—southern Indian Ocean. + + + +Species + +Oloughlinia discoveryi + +(Heding in +Heding & Panning, 1954 +) nov. comb. + +—South Atlantic Ocean. + + + + \ No newline at end of file diff --git a/data/38/78/AB/3878AB0B994527CA4A5499DBB451C22A.xml b/data/38/78/AB/3878AB0B994527CA4A5499DBB451C22A.xml new file mode 100644 index 00000000000..27d4a8b010c --- /dev/null +++ b/data/38/78/AB/3878AB0B994527CA4A5499DBB451C22A.xml @@ -0,0 +1,71 @@ + + + +Cyanobacteria of Greece: an annotated checklist + + + +Author + +Gkelis, Spyros + + + +Author + +Ourailidis, Iordanis + + + +Author + +Panou, Manthos + + + +Author + +Pappas, Nikos + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +10084 +10084 + + + + +http://dx.doi.org/10.3897/BDJ.4.e10084 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e10084 +1314-2828--10084 + + + + +Chroococcidiopsis kashayi Friedmann, 1961 + + + + +Chroococcidiopsis kashaii + + + +Notes + +Lamprinou et al. 2012 + + + + \ No newline at end of file diff --git a/data/38/79/22/3879220E4C7D840C9A7A706BDCD32E86.xml b/data/38/79/22/3879220E4C7D840C9A7A706BDCD32E86.xml new file mode 100644 index 00000000000..ff6f980baad --- /dev/null +++ b/data/38/79/22/3879220E4C7D840C9A7A706BDCD32E86.xml @@ -0,0 +1,83 @@ + + + +Order Soricomorpha + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +220 +311 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Sorex (Sorex) gracillimus +subsp. +gracillimus +Thomas 1907 + + + + + + + +Sorex (Sorex) gracillimus +subsp. +gracillimus +Thomas 1907 + +, +Proc. Zool. Soc. Lond., 1907: 408 + +. + + + + +Type Locality: + +Russia +, +Sakhalin +Isl, "Dariné, +25 miles +[ +40 km +] N.W. of Korsakoff, Saghalien". + + + + + \ No newline at end of file diff --git a/data/38/79/69/387969A01383DBD4F96D50D3C0FD00E3.xml b/data/38/79/69/387969A01383DBD4F96D50D3C0FD00E3.xml new file mode 100644 index 00000000000..076a4e155d1 --- /dev/null +++ b/data/38/79/69/387969A01383DBD4F96D50D3C0FD00E3.xml @@ -0,0 +1,74 @@ + + + +Brachiopoda of Greece: an annotated checklist + + + +Author + +Gerovasileiou, Vasilis + + + +Author + +Bailly, Nicolas + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8169 +8169 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8169 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8169 +1314-2828-4-8169 + + + + + +Novocrania anomala ( +Mueller +, 1776) + + + + +Distribution +North Aegean, South Aegean, Levantine Sea, Ionian Sea + + +Horizon +Pleistocene, Pliocene, Holocene + + +Notes + +Recorded by +Logan (1979) +, +Morri et al. (1999) +, +Logan et al. (2002) +, +Gerovasileiou et al. (2015) +. Habitat/Substrate: Caves, precoralligenous, coralligenous, bioconcretions, banks, boulders, muddy sand, coarse sand. Depth: 2-150 m. + + + + \ No newline at end of file diff --git a/data/38/79/98/3879983D5C25E680865360A163CDF372.xml b/data/38/79/98/3879983D5C25E680865360A163CDF372.xml new file mode 100644 index 00000000000..3f3db63b9d6 --- /dev/null +++ b/data/38/79/98/3879983D5C25E680865360A163CDF372.xml @@ -0,0 +1,71 @@ + + + +Checklist of British and Irish Hymenoptera - Braconidae + + + +Author + +Broad, Gavin R. + + + +Author + +Shaw, Mark R. + + + +Author + +Godfray, H. Charles J. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8151 +8151 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8151 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8151 +1314-2828--8151 + + + + +Dinotrema (Dinotrema) divisum (Stelfox & Graham, 1950) + + + + +Aspilota divisa +Stelfox & Graham, 1950 + + +aureliae +(Fischer, 1973, +Aspilota +); tentative synonymy by +Papp (2004b) + + + +Distribution +England, Scotland, Ireland + + + \ No newline at end of file diff --git a/data/38/79/FB/3879FB0F480F51E6B4B3C1C667A62980.xml b/data/38/79/FB/3879FB0F480F51E6B4B3C1C667A62980.xml new file mode 100644 index 00000000000..e182a4c666c --- /dev/null +++ b/data/38/79/FB/3879FB0F480F51E6B4B3C1C667A62980.xml @@ -0,0 +1,115 @@ + + + +Nomenclatural changes in Coleus and Plectranthus (Lamiaceae): a tale of more than two genera + + + +Author + +Paton, Alan J. + + + +Author + +Mwanyambo, Montfort + + + +Author + +Govaerts, Rafael H. A. + + + +Author + +Smitha, Kokkaraniyil + + + +Author + +Suddee, Somran + + + +Author + +Phillipson, Peter B. + + + +Author + +Wilson, Trevor C. + + + +Author + +Forster, Paul I. + + + +Author + +Culham, Alastair + +text + + +PhytoKeys + + +2019 + +129 + + +1 +158 + + + + +http://dx.doi.org/10.3897/phytokeys.129.34988 + +journal article +http://dx.doi.org/10.3897/phytokeys.129.34988 +1314-2003-129-1 +BF57C6B3C3065AEE9B4B3D47189C908F +3382366 + + + + +Coleus arabicus Benth. in A.P. de Candolle, Prodr. 12: 79. 1848 + + + + +Majana arabica +(Benth.) Kuntze, Revis. Gen. Pl. 2: 524. 1891. Type: Arabia, +Botta +s.n. (holotype: P). + + +Plectranthus asirensis +J +.R.I.Wood, Kew Bull. 37: 601. 1983. Type: Saudi Arabia, Taif, +Botta +s.n. (holotype: P; isotype K). + + +Teucrium mazziarii +Heldr. ex Nyman, Consp. Fl. Eur.: 567. 1881, nom. inval. + + + +Distribution. +Arabian Peninsula. + + + \ No newline at end of file diff --git a/data/38/7A/2E/387A2E88306DC9B30157BA8115533755.xml b/data/38/7A/2E/387A2E88306DC9B30157BA8115533755.xml new file mode 100644 index 00000000000..8e5ce9264cc --- /dev/null +++ b/data/38/7A/2E/387A2E88306DC9B30157BA8115533755.xml @@ -0,0 +1,833 @@ + + + +Biodiversity inventories in high gear: DNA barcoding facilitates a rapid biotic survey of a temperate nature reserve + + + +Author + +Telfer, Angela C +Biodiversity Institute of Ontario, Guelph, Canada +atelfer@uoguelph.ca + + + +Author + +Young, Monica R +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Quinn, Jenna +rare Charitable Research Reserve, Cambridge, Canada + + + +Author + +Perez, Kate +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Sobel, Crystal N +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Sones, Jayme E +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Levesque-Beaudin, Valerie +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Derbyshire, Rachael +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Fernandez-Triana, Jose +CNC, Ottawa, Canada +https://orcid.org/0000-0003-0425-0309 + + + +Author + +Rougerie, Rodolphe +Museum national d'Histoire Naturelle, Paris, France + + + +Author + +Thevanayagam, Abinah +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Boskovic, Adrian +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Borisenko, Alex V +Biodiversity Institute of Ontario, Guelph, Canada +https://orcid.org/0000-0002-3061-3057 + + + +Author + +Cadel, Alex +University of Waterloo, Waterloo, Canada + + + +Author + +Brown, Allison +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Pages, Anais +Universite de Montpellier, Montpellier, France + + + +Author + +Castillo, Anibal H +Biodiversity Institute of Ontario, Guelph, Canada +https://orcid.org/0000-0002-1537-0528 + + + +Author + +Nicolai, Annegret +EcoBio, Universite of Rennes, Rennes, France + + + +Author + +Glenn Mockford, Barb Mockford +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Bukowski, Belen +Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " (MACN-CONICET), Buenos Aires, Argentina + + + +Author + +Wilson, Bill +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Trojahn, Brock +rare Charitable Research Reserve, Cambridge, Canada + + + +Author + +Lacroix, Carole Ann +Biodiversity Institute of Ontario Herbarium, Guelph, Canada + + + +Author + +Brimblecombe, Chris +University of Waikato, Hamilton, New Zealand + + + +Author + +Hay, Christoper +University of Western Ontario, London, Canada + + + +Author + +Ho, Christmas +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Steinke, Claudia +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Warne, Connor P +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Garrido Cortes, Cristina +University of Guelph, Guelph, Canada + + + +Author + +Engelking, Daniel +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Wright, Danielle +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Lijtmaer, Dario A +Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " (MACN-CONICET), Buenos Aires, Argentina + + + +Author + +Gascoigne, David +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Hernandez Martich, David +Universidad Autonoma de Santo Domingo DR, Santo Domingo, Dominican Republic + + + +Author + +Morningstar, Derek +Myotistar, Cambridge, Canada + + + +Author + +Neumann, Dirk +SNSB, Zoologische Staatssammlung Muenchen, Munich, Germany + + + +Author + +Steinke, Dirk +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Marco DeBruin, Donna DeBruin +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Dobias, Dylan +University of Guelph, Guelph, Canada + + + +Author + +Sears, Elizabeth +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Richard, Ellen +University of Guelph, Guelph, Canada + + + +Author + +Damstra, Emily +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Zakharov, Evgeny V +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Laberge, Frederic +University of Guelph, Guelph, Canada + + + +Author + +Collins, Gemma E +University of Waikato, Hamilton, New Zealand + + + +Author + +Blagoev, Gergin A +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Grainge, Gerrie +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Ansell, Graham +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Meredith, Greg +Grand River Conservation Authority, Guelph, Canada + + + +Author + +Hogg, Ian +University of Waikato, Hamilton, New Zealand + + + +Author + +McKeown, Jaclyn +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Topan, Janet +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Bracey, Jason +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Guenther, Jerry +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Sills-Gilligan, Jesse +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Addesi, Joseph +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Persi, Joshua +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Layton, Kara K S +The University of Western Australia, Perth, Australia + + + +Author + +D'Souza, Kareina +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Dorji, Kencho +National Biodiversity Centre, Thimphu, Bhutan + + + +Author + +Grundy, Kevin +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Nghidinwa, Kirsti +Ministry of Environment and Tourism in Namibia, Windhoek, Namibia + + + +Author + +Ronnenberg, Kylee +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Lee, Kyung Min +University of Oulu, Oulu, Finland + + + +Author + +Xie, Linxi +The University of Western Ontario, London, Canada + + + +Author + +Lu, Liuqiong +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Penev, Lyubomir +Pensoft, Sofia, Bulgaria +https://orcid.org/0000-0002-2186-5033 + + + +Author + +Gonzalez, Mailyn +Instituto de Investigacion de Recursos Biologicos Alexander von Humboldt, Bogota, Colombia + + + +Author + +Rosati, Margaret E +Smithsonian National Museum of Natural History, Washington, United States of America + + + +Author + +Kekkonen, Mari +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Kuzmina, Maria +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Iskandar, Marianne +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Mutanen, Marko +University of Oulu, Oulu, Finland + + + +Author + +Fatahi, Maryam +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Pentinsaari, Mikko +University of Oulu, Oulu, Finland + + + +Author + +Bauman, Miriam +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Nikolova, Nadya +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Ivanova, Natalia V +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Jones, Nathaniel +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Weerasuriya, Nimalka +The University of Western Ontario, London, Canada + + + +Author + +Monkhouse, Norman +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Lavinia, Pablo D +Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " (MACN-CONICET), Buenos Aires, Argentina + + + +Author + +Jannetta, Paul +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Hanisch, Priscila E +Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " (MACN-CONICET), Buenos Aires, Argentina + + + +Author + +McMullin, R. Troy +Biodiversity Institute of Ontario Herbarium, Guelph, Canada + + + +Author + +Ojeda Flores, Rafael +Universidad Nacional Autonoma de Mexico, Mexico City, Mexico + + + +Author + +Mouttet, Raphaelle +ANSES, Laboratoire de la Sante des Vegetaux, Montferrier sur Lez, France + + + +Author + +Vender, Reid +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Labbee, Renee N +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Forsyth, Robert +New Brunswick Museum, Saint John, Canada +https://orcid.org/0000-0002-9637-0158 + + + +Author + +Lauder, Rob +London Homeopathy, London, Canada + + + +Author + +Dickson, Ross +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Kroft, Ruth +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Miller, Scott E +Smithsonian National Museum of Natural History, Washington, United States of America + + + +Author + +MacDonald, Shannon +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Panthi, Sishir +Ministry of Forests and Soil Conservation, Kathmandu, Nepal + + + +Author + +Pedersen, Stephanie +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Sobek-Swant, Stephanie +rare Charitable Research Reserve, Cambridge, Canada + + + +Author + +Naik, Suresh +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Lipinskaya, Tatsiana +Scientific and Practical Center for Bioresources, National Academy of Sciences of Belarus, Minsk, Belarus + + + +Author + +Eagalle, Thanushi +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Decaens, Thibaud +Universite de Montpellier Centre d'Ecologie Fonctionnelle et Evolutive, Montpellier, France + + + +Author + +Kosuth, Thibault +Universite de Montpellier, Montpellier, France + + + +Author + +Braukmann, Thomas +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Woodcock, Tom +rare Charitable Research Reserve, Cambridge, Canada + + + +Author + +Roslin, Tomas +University of Helsinki, Helsinki, Finland + + + +Author + +Zammit, Tony +Grand River Conservation Authority, Cambridge, Canada + + + +Author + +Campbell, Victoria +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Dinca, Vlad +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Peneva, Vlada +Bulgarian Academy of Sciences, Sofia, Bulgaria + + + +Author + +Hebert, Paul D N +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +deWaard, Jeremy R +Biodiversity Institute of Ontario, Guelph, Canada +dewaardj@uoguelph.ca + +text + + +Biodiversity Data Journal + + +2015 + +3 + + +6313 +6313 + + + + +http://dx.doi.org/10.3897/BDJ.3.e6313 + +journal article +http://dx.doi.org/10.3897/BDJ.3.e6313 +1314-2828-3-e6313 +FFE5FF837519E9253D17614AFFA8FFC1 +574474 + + + + +Philothermus glabriculus LeConte, 1863 + + + +Notes +BOLD:ABX9329 + + + \ No newline at end of file diff --git a/data/38/7A/84/387A840214F72318B697A81A441E6A30.xml b/data/38/7A/84/387A840214F72318B697A81A441E6A30.xml new file mode 100644 index 00000000000..4d04c77062e --- /dev/null +++ b/data/38/7A/84/387A840214F72318B697A81A441E6A30.xml @@ -0,0 +1,51 @@ + + + +Catalogue of the hymenopterous insects collected at Sarawak, Borneo; Mount Ophir, Malacca; and at Singapore, by A. R. Wallace. + + + +Author + +Smith, F. + +text + + +Journal of the Proceedings of the Linnean Society of London, Zoology + + +1857 + +2 + + +42 +88 + + + + +http://antbase.org/ants/publications/2588/2588.pdf + +journal article +2588 +D09C3FFA-7EB5-4A2D-A55E-A3229619A2A2 + + + + +9. +Trigona fimbriata +. + + + +T. capite thorace que femoribus et abdomine basi testaceo-rufis; tibiis tarsisque intermediis et posticis nigris. +Worker, Length 3 1/2 lines. Head rufo-testaceous, the face covered with very short ochraceous pubescence, and sprinkled with longer stiff black hairs; the colour and pubescence of the thorax are similar to that of the head, but the disk is of a rather darker colour, and the black hairs are longer and more rigid; the intermediate and posterior tibiae, and the basal joints of their tarsi, black, the former densely covered with black pubescence, and the latter thickly fringed with the same, the posterior tibiae being very broadly dilated towards their apex; the wings hyaline, their nervures bright ferruginous. Abdomen: the two basal segments rufo-testaceous, their apical margins, as well as the whole of the following segments, nigro-fuscous. + + +Hab. Singapore. + + + \ No newline at end of file diff --git a/data/38/7A/BA/387ABAA8C0A95DB0B0709B6C4FB7918C.xml b/data/38/7A/BA/387ABAA8C0A95DB0B0709B6C4FB7918C.xml new file mode 100644 index 00000000000..5c391c2cb4b --- /dev/null +++ b/data/38/7A/BA/387ABAA8C0A95DB0B0709B6C4FB7918C.xml @@ -0,0 +1,167 @@ + + + +Biting midges of Egypt (Diptera: Ceratopogonidae) + + + +Author + +El-Hawagry, Magdi S. +Entomology Department, Faculty of Science, Cairo University, Giza, Egypt +https://orcid.org/0000-0001-9162-5265 +elhawagry@gmail.com + + + +Author + +El-Azab, Salah El-Din A. +Insect Taxonomy Department, Plant Protection Research Institute, Dokki, Giza, Egypt + + + +Author + +Abdel-Dayem, Mahmoud S. +College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia +https://orcid.org/0000-0002-6276-1740 + + + +Author + +Al Dhafer, Hathal M. +College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia +https://orcid.org/0000-0002-4911-2332 + +text + + +Biodiversity Data Journal + + +2020 + +8 + + +52357 +52357 + + + + +http://dx.doi.org/10.3897/BDJ.8.e52357 + +journal article +http://dx.doi.org/10.3897/BDJ.8.e52357 +1314-2828-8-e52357 +CEB65C20D7855AD294A989CBC7F67ED6 + + + + +Forcipomyia (Synthyridomyia) murina (Winnertz, 1852) + + + + +Ceratopogon murinus +Winnertz, 1852 [ +Winnertz 1852 +: 26]. Type locality: Europe. + + +Helea murina var. abdominalis +Santos Abreu, 1918 [ +Santos Abreu 1918 +: 265]. Type locality: Canary Islands (Spain). + + +Apelma aurosparsum +Kieffer, 1919 [ +Kieffer 1919 +: 65]. Type locality: Hungary. + + +Forcipomyia sulfurea +Kieffer, 1923 [ +Kieffer 1923a +: 664]. Type locality: Algeria. + + +Forcipomyia hirtipalpis +Kieffer, 1924 [ +Kieffer 1924b +: 392]. Type locality: France. + + +Forcipomyia sate +Kieffer, 1925 [ + +Kieffer 1925c + +: 245]. Type locality: Egypt. + + +Forcipomyia longitarsis +Tokunaga, 1940 [ + +Tokunaga 1940 + +: 92], preoccupied by + +Forcipomyia longitarsis + +(Malloch 1915b). Type locality: Taiwan. + + +Forcipomyia moascari +Macfie, 1943 [ +Macfie 1943 +: 147]. Type locality: Egypt. + + +Forcipomyia attonsa +Goetghebuer, 1950 [ +Goetghebuer 1950 +: 1]. Type locality: Belgium. + + +Forcipomyia tokunagai +Wirth, 1973: 356 [ +Wirth 1973 +], preoccupied by + +Forcipomyia tokunagai + +( +Oka and Asahina 1948 +). New name for + +longitarsis + +. + + +Forcipomyia submurina +Remm, 1980 [ +Remm 1980 +: 115], as +sibmurina +, as subspecies of + +murina + +. Type locality: Russia. + + + +Distribution +Widespread in AF, PA and NE. +Local distribution in Egypt: Coastal Strip: Alexandria (Sidi Gaber). Eastern Desert: Ismailia (Moascar), Suez (Guyot Garden). Lower Nile Valley & Delta: El-Qanatir, Maadi. Upper Nile Valley: Asswan. +Dates of collection in Egypt: August to April. + + + \ No newline at end of file diff --git a/data/38/7A/BB/387ABB0EC0726B6CB90EE94CB2408B0A.xml b/data/38/7A/BB/387ABB0EC0726B6CB90EE94CB2408B0A.xml new file mode 100644 index 00000000000..b1910358bfb --- /dev/null +++ b/data/38/7A/BB/387ABB0EC0726B6CB90EE94CB2408B0A.xml @@ -0,0 +1,271 @@ + + + +Info Flora Schweiz - Poaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/poaceae.html + +url + + + + + +Alopecurus alpinus +Vill. + + + + + +Art ISFS: 25600 Checklist: 1002890 +Poaceae +Alopecurus +Alopecurus alpinus Vill. + + + +Bestimmungsschluessel + + + +Zusammenfassung +KEINE ANGABE Anatomie + + +Zusammenfassung der Stammanatomie + + +Umriss rund oder oval. +Leitbuendel +in einer Reihe. Epidermiszellen verholzt. Chlorenchyma in tangential +verlaengerten +Gruppen. + + +Beschreibung (Englisch) + + +Culm-diameter < +0.5 mm +, wall large, radius of culm in relation to wall thickness 1:0.5. Outline circular with a smooth surface. Culm-center hollow and surrounded by a few thin-walled, not lignified cells. Epidermis with hairs. Epidermis-cells thick-walled all around. Large vascular bundles arranged in one peripheral row. Chlorenchyma in tangentially enlarged groups. Sclerenchyma in a large, peripheral continuous belt (> 3 cells). Cells medium thick-walled. Small sclerenchymatic sheath with 1-2 cells around vascular bundles. Largest vessels in vascular bundles in lateral position. Largest vessel in the bundle small, <20μm. + + + +Oekologie + + + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + + + + + +
KEINE ANGABE
+
+
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F--Lichtzahl L--Salzzeichen--
Reaktionszahl R--Temperaturzahl T--
+Naehrstoffzahl +N +-- +Kontinentalitaetszahl +K +--
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Alopecurus alpinus +Vill. + + + + + +Volksname + + + +Deutscher Name: -- Nom +francais +: -- Nome italiano: -- + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Alopecurus alpinus Vill. + + +Checklist 2017 + +25600
= +Alopecurus alpinus Vill. + + +Index synonymique 1996 + +25600
= +Alopecurus alpinus Vill. + + +SISF/ISFS 2 + +25600
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Kommentare aus der +Checklist 2017 +Wird in Euro+Med unter dem Namen + +Alopecurus magellanicus +Lam. + +gefuehrt +. Checklist + + + + +Status Indigenat +: - + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein + + +
+
\ No newline at end of file diff --git a/data/38/7A/C2/387AC21DFFB01874FF13F96142E2C46C.xml b/data/38/7A/C2/387AC21DFFB01874FF13F96142E2C46C.xml new file mode 100644 index 00000000000..146eead45b2 --- /dev/null +++ b/data/38/7A/C2/387AC21DFFB01874FF13F96142E2C46C.xml @@ -0,0 +1,443 @@ + + + +Notes on rattans (Arecaceae) from Vietnam + + + +Author + +Henderson, Andrew +Institute of Systematic Botany, The New York Botanical Garden, Bronx, NY 10458 - 5126, U. S. A. E-mail: ahenderson @ nybg. org Forest Inventory and Planning Institute, Thanh Tri, Hanoi, Vietnam E-mail: dungfipi @ gmail. com + + + +Author + +Dung, Nguyen Quoc + +text + + +Phytotaxa + + +2010 + +2010-08-31 + + +8 + + +25 +33 + + + +journal article +6328 +10.11646/phytotaxa.8.1.2 +ccbf0321-20dc-4799-8575-3f018b87afcc +1179-3163 +4893981 + + + + + + + +Plectocomiopsis songthanhensis +A.J.Hend. & N.Q.Dung + +, + + +sp. nov +. + +( +Plate 1 +) + + + + + + +A +Plectocomiopsis geminiflora pinnis +glabris et floribus glabris differt. + + + + + + +Type +:— +VIETNAM +. +Quang Nam Province +: +Nam Giang District +, +Ta Bhing +commune, +Song Thanh Nature Reserve +, road 14 D to +Laos +, 15˚39’ +N + +, + +107˚36’ +E +, + +412 m + +, + +12 March 2009 + +, + +A + + + +. + +Henderson +, +B +. +V + +. + +Thanh +, +N +. +T + +. + +Vu +& +C + +. + + + +Tuo +3573 + +( +holotype +: +HN +!, isotypes: +AAU +! +K +! +NY +!) + +. + + + + +Stems clustered, forming large clumps, +20–30 m +tall, +1.5–1.7 cm +in diameter with sheaths, triangular in cross–section. Leaf sheaths green or gray-green, with few, scattered, yellowish spines to +5 mm +long; knees absent; ocreas to +1 cm +long, green, membranous, with few, short spines, becoming brown and splitting irregularly; petioles absent or to +2 cm +long; rachis +56–87 cm +long, with recurved spines abaxially; pinnae 11– 13 per side of rachis, more or less regularly and distantly arranged; middle pinnae +25–27 cm +long, +1.5–3 cm +wide at widest point, lanceolate, with long, filiform apices, with prominent cross–veins, without bristles; cirri +60–80 cm +long. Inflorescences 9–11 at apex of stem, subtended by reduced leaves, branched to 2 orders, pendulous; staminate inflorescences with 19–29 rachillae, these +9–23 cm +long, +1.5 mm +in diameter; staminate flowers borne in short, congested rows on opposite sides of rachillae to +1 cm +long; staminate flowers globose in bud, +1.2 mm +long (immature); sepals glabrous, +1 mm +long; petals 3, free, valvate, glabrous, +1 mm +long; pistillate inflorescences with 11 rachillae, these +7–12 cm +long, +2.5 mm +in diameter; pistillate flowers paired on very short rachillae subtended by a cupular bracteole; pistillate flowers not seen; fruits depressed–globose, +1.6–1.8 cm +in diameter, brownish–green; endosperm homogeneous. + + + + +PLATE 1. + +Plectocomiopsis songthanhensis + +. Left—habit. Right—fruits. + + + + +Distribution and habitat:— +Endemic to central +Vietnam +in +Quang Nam +and +Thua Thien-Hue +Provinces, in disturbed places by roads or in disturbed areas in forest. + + + + +Local names and uses:— +may phun, may rut +. The cane is of poor quality and is collected only for domestic uses. + + + + + + +Additional specimens examined ( +paratypes +):— + +VIETNAM +. +Thua Thien-Hue +: +Bach Ma National Park +, +16°14’N +, +107°52’E +, ca. + +100 m + +, + +14 April 2007 + +, +Henderson et al. 3277 +( +HN +, +NY +) + +. + +Quang Nam +: Nam Giang district, + +17 October 2005 + +, + +N +. +K +. +Ban +PA 167 + +( +HN +); + + +Nam Giang District +, +Ta Bhing +commune, +Song Thanh Nature Reserve +, road 14 D to +Laos +, 15˚39’ +N +, 107˚36’ +E +, + +412 m + +, + +12 March 2009 + +, + +Henderson +et al. 3571 + +( +AAU +, +HN +, +K +, +NY +); +3572 +( +AAU +, +HN +, +K +, +NY +); + +14 Mar 2009 + +, +3577 +( +AAU +, +HN +, +K +, +NY +); +3581 +( +HN +, +K +, +NY +); + + +Ho Chi Minh Highway +between Thanh My and Prao +, 15˚48’ +N +, 107˚45’ +E +, + +294 m + +, + +19 March 2009 + +, + +Henderson +et al. 3594 + +( +HN +, +NY +) + +. + + + + +Discussion: +— + +Plectocomiopsis songthanhensis + +(named for the Song Thanh Nature Reserve) differs from + +P. geminiflora + +in its pinnae without bristles (versus pinnae with conspicuous bristles along adaxial mid–veins and margins); short, entire, non-tattering ocreas (versus elongate, tattering ocreas); petioles without marginal spines (versus petioles with marginal spines); staminate calyces split to the base into 3, free sepals (versus staminate calyces cupular, briefly and irregularly 3–lobed); and glabrous staminate and pistillate perianths (versus staminate and pistillate perianths usually covered with scale–like trichomes). + + + + +The distributions of the two species do not overlap. + +Plectocomiopsis songthanhensis + +is known only from central +Vietnam +in +Quang Nam +and Thua Thien–Hue Provinces. In +Vietnam +, + +P. geminiflora + +is known only from southern part of the country, in +Dong Nai +and +Lam Dong +Provinces, although it is widely distributed elsewhere ( +Cambodia +, +Laos +, +Myanmar +, +Thailand +, Borneo, Peninsular +Malaysia +, and Sumatra). Three specimens of + +Plectocomiopsis + +at K ( +Khamphone 393, 409, Sounthone 22 +) from +Laos +occur relatively near to the population of + +P. songthanhensis + +. Although all +three specimens +are sterile, they share bristly pinnae, tattering ocreas, and spiny petioles, and are identified as + +P. geminiflora +(Evans +et al. +2002) + +. + + + + \ No newline at end of file diff --git a/data/38/7A/C2/387AC21DFFB01876FF13FA60449BC186.xml b/data/38/7A/C2/387AC21DFFB01876FF13FA60449BC186.xml new file mode 100644 index 00000000000..dc691f99ff6 --- /dev/null +++ b/data/38/7A/C2/387AC21DFFB01876FF13FA60449BC186.xml @@ -0,0 +1,78 @@ + + + +Notes on rattans (Arecaceae) from Vietnam + + + +Author + +Henderson, Andrew +Institute of Systematic Botany, The New York Botanical Garden, Bronx, NY 10458 - 5126, U. S. A. E-mail: ahenderson @ nybg. org Forest Inventory and Planning Institute, Thanh Tri, Hanoi, Vietnam E-mail: dungfipi @ gmail. com + + + +Author + +Dung, Nguyen Quoc + +text + + +Phytotaxa + + +2010 + +2010-08-31 + + +8 + + +25 +33 + + + +journal article +6328 +10.11646/phytotaxa.8.1.2 +ccbf0321-20dc-4799-8575-3f018b87afcc +1179-3163 +4893981 + + + + + + + +Plectocomiopsis +Beccari + +in Hooker (1893: 479) + + + + + + +Until now (Henderson, 2009) one species of + +Plectocomiopsis + +was known from +Vietnam +: + +Plectocomiopsis geminiflora +(Griffith) Beccari + +in Hooker (1893: 479). During recent field work in central +Vietnam +, a second species was discovered and is described below. + + + + \ No newline at end of file diff --git a/data/38/7A/C2/387AC21DFFB21874FF16FA8146F3C167.xml b/data/38/7A/C2/387AC21DFFB21874FF16FA8146F3C167.xml new file mode 100644 index 00000000000..74d2ec0339e --- /dev/null +++ b/data/38/7A/C2/387AC21DFFB21874FF16FA8146F3C167.xml @@ -0,0 +1,196 @@ + + + +Notes on rattans (Arecaceae) from Vietnam + + + +Author + +Henderson, Andrew +Institute of Systematic Botany, The New York Botanical Garden, Bronx, NY 10458 - 5126, U. S. A. E-mail: ahenderson @ nybg. org Forest Inventory and Planning Institute, Thanh Tri, Hanoi, Vietnam E-mail: dungfipi @ gmail. com + + + +Author + +Dung, Nguyen Quoc + +text + + +Phytotaxa + + +2010 + +2010-08-31 + + +8 + + +25 +33 + + + +journal article +6328 +10.11646/phytotaxa.8.1.2 +ccbf0321-20dc-4799-8575-3f018b87afcc +1179-3163 +4893981 + + + + + + + +Daemonorops fissilis +(A.J.Hend., N.K.Ban & N.Q.Dung) A.J.Hend. + +, + +comb. nov. + + + + + + + +Basionym: + + +Calamus fissilis +Henderson +et al. +(2008: 192) + +. + + + + + +Type +:— +VIETNAM +. +Thua Thien-Hue +: +Bach Ma National Park +, +16°14’N +, +107°52’E +, + +100 m + +, + +12 April 2007 + +, + +A + + + +. + +Henderson +, +N +. +Q + +. + +Dung +, +P + +. + +X. +Phuong +, & +L +. +V + +. + + + +Bo +3266 + +( +holotype +: +HN +!, isotypes: +K +! +NY +!) + +. + + +Additional material studied:— + +VIETNAM +: +Da Nang +City +, +Hoa Vang District +, +Ba Na-Nui Chua Nature Reserve +, steep forested slopes, +16°00’N +, +108°01’E +, ca. + +800 m + +, + +4 Jun 2009 + +, + +Henderson & +N + + + +. + +K + +. + + + +Ban +3596 + +( +HN +, +NY +) + +. + + + + \ No newline at end of file diff --git a/data/38/7A/C2/387AC21DFFB21874FF16FC034570C3E9.xml b/data/38/7A/C2/387AC21DFFB21874FF16FC034570C3E9.xml new file mode 100644 index 00000000000..6e8f138db79 --- /dev/null +++ b/data/38/7A/C2/387AC21DFFB21874FF16FC034570C3E9.xml @@ -0,0 +1,93 @@ + + + +Notes on rattans (Arecaceae) from Vietnam + + + +Author + +Henderson, Andrew +Institute of Systematic Botany, The New York Botanical Garden, Bronx, NY 10458 - 5126, U. S. A. E-mail: ahenderson @ nybg. org Forest Inventory and Planning Institute, Thanh Tri, Hanoi, Vietnam E-mail: dungfipi @ gmail. com + + + +Author + +Dung, Nguyen Quoc + +text + + +Phytotaxa + + +2010 + +2010-08-31 + + +8 + + +25 +33 + + + +journal article +6328 +10.11646/phytotaxa.8.1.2 +ccbf0321-20dc-4799-8575-3f018b87afcc +1179-3163 +4893981 + + + + + + + +Daemonorops +Blume + +in Roemer & Schultes (1830:1333) + + + + + + + +Calamus fissilis +Henderson +et al. +(2008: 192) + +and + +C. nuichuaensis +Henderson +et al. +(2008: 196) + +were based on incomplete specimens. Recently we have collected more complete specimens of both species. These have the inflorescence rachis bracts splitting to the base and becoming deciduous, and fruits with ruminate endosperm. These two character states are not found in + +Calamus +, + +but are common in + +Daemonorops + +, and therefore we transfer both these species to + +Daemonorops + +. Based on the deciduous, splitting rachis bracts, the two species appear to belong to section +Piptoshatha +Beccari (1911: 27). + + + + \ No newline at end of file diff --git a/data/38/7A/C2/387AC21DFFB21875FF16F93C4723C663.xml b/data/38/7A/C2/387AC21DFFB21875FF16F93C4723C663.xml new file mode 100644 index 00000000000..847602b9d53 --- /dev/null +++ b/data/38/7A/C2/387AC21DFFB21875FF16F93C4723C663.xml @@ -0,0 +1,186 @@ + + + +Notes on rattans (Arecaceae) from Vietnam + + + +Author + +Henderson, Andrew +Institute of Systematic Botany, The New York Botanical Garden, Bronx, NY 10458 - 5126, U. S. A. E-mail: ahenderson @ nybg. org Forest Inventory and Planning Institute, Thanh Tri, Hanoi, Vietnam E-mail: dungfipi @ gmail. com + + + +Author + +Dung, Nguyen Quoc + +text + + +Phytotaxa + + +2010 + +2010-08-31 + + +8 + + +25 +33 + + + +journal article +6328 +10.11646/phytotaxa.8.1.2 +ccbf0321-20dc-4799-8575-3f018b87afcc +1179-3163 +4893981 + + + + + + + +Daemonorops nuichuaensis +(A.J.Hend., N.K.Ban & N.Q.Dung) A.J.Hend. + +, + +comb. nov +. + + + + + + + +Basionym +:— + +Calamus nuichuaensis +Henderson +et al. +(2008: 196) + +. + + + + + + +<location id="B50C25D0FFB21874FF47F8884722C01F" LSID="urn:lsid:plazi:treatment:387AC21DFFB21875FF16F93C4723C663:B50C25D0FFB21874FF47F8884722C01F" box="[198,259,1814,1840]" county="Nui Chua National Park" latitude="11.8" longLatPrecision="1294" longitude="109.166664" municipality="Ninh Hai District" name="Type" pageId="2" pageNumber="27">Type</location> +:—VIETNAM. +<location id="B50C25D0FFB21874FE3CF8884471C01F" LSID="urn:lsid:plazi:treatment:387AC21DFFB21875FF16F93C4723C663:B50C25D0FFB21874FE3CF8884471C01F" box="[445,592,1814,1840]" county="Nui Chua National Park" latitude="11.8" longLatPrecision="1294" longitude="109.166664" municipality="Ninh Hai District" name="Ninh Thuan" pageId="2" pageNumber="27">Ninh Thuan</location> + +: + +Ninh Hai District +, +Nui Chua National Park + +, +near summit of mountain, forest on rocky slopes +, + +11 +° +48 +’N + +, +109°10’E +, ca. + +800 m + +, +27 July 2007 +, + +A. Henderson +, +N.K. Ban +, & +A R. Cui +3468 + +(holotype: HN!, isotypes: K! NY!) + +. + + + +Additional material studied:— +<materialsCitation id="00BB7956FFB21874FDAEF81445ECC08B" ID-GBIF-Occurrence="3125612313" box="[559,973,1930,1956]" collectingDate="2009-10-26" county="Nui Chua National Park" elevation="800" latitude="11.8" location="Ninh Thuan Province" longLatPrecision="776" longitude="109.16" municipality="Ninh Hai District" pageId="2" pageNumber="27" specimenCount="1"> +VIETNAM. +<location id="B50C25D0FFB21874FD49F81445ECC08B" LSID="urn:lsid:plazi:treatment:387AC21DFFB21875FF16F93C4723C663:B50C25D0FFB21874FD49F81445ECC08B" box="[712,973,1930,1956]" county="Nui Chua National Park" latitude="11.8" longLatPrecision="776" longitude="109.16" municipality="Ninh Hai District" name="Ninh Thuan Province" pageId="2" pageNumber="27">Ninh Thuan Province</location> +</materialsCitation> + +: + +Ninh Hai District +, +Nui Chua National Park + +, + +11.80N +, +109.16E +, ca. + + + +800 +m + + +, +26 Oct 2009 +, + +Henderson et al. +3646 + +(HN, NY). + + +The transfer of these two species brings the number of + +Daemonorops +in Vietnam + +to five: +D. jenkinsiana +(Griffith) Martius ( +1853 +: 327), +D. poilanei +Dransfield (2001: 663), +D. mollispina +Dransfield ( +2001 +: 662), +D. fissilis +and +D. nuichuaensis +. All but +D. jenkinsiana +are endemic to Vietnam and belong to section +Piptospatha +. Recent field work revealed another two species new to science, making a total of seven +Daemonorops +for Vietnam. + + + + \ No newline at end of file diff --git a/data/38/7A/C2/387AC21DFFB31872FF16FE3846FDC5AD.xml b/data/38/7A/C2/387AC21DFFB31872FF16FE3846FDC5AD.xml new file mode 100644 index 00000000000..54d833fe933 --- /dev/null +++ b/data/38/7A/C2/387AC21DFFB31872FF16FE3846FDC5AD.xml @@ -0,0 +1,232 @@ + + + +Notes on rattans (Arecaceae) from Vietnam + + + +Author + +Henderson, Andrew +Institute of Systematic Botany, The New York Botanical Garden, Bronx, NY 10458 - 5126, U. S. A. E-mail: ahenderson @ nybg. org Forest Inventory and Planning Institute, Thanh Tri, Hanoi, Vietnam E-mail: dungfipi @ gmail. com + + + +Author + +Dung, Nguyen Quoc + +text + + +Phytotaxa + + +2010 + +2010-08-31 + + +8 + + +25 +33 + + + +journal article +6328 +10.11646/phytotaxa.8.1.2 +ccbf0321-20dc-4799-8575-3f018b87afcc +1179-3163 +4893981 + + + + + + + +Daemonorops brevicaulis +A.J.Hend. & N.Q.Dung + +, + +sp. nov. + + +( +Plate 2 +) + + + + + + +A speciebus aliis +Daemonorops habitu +non scandenti et foliis non cirratis differt. + + + + + + +Type +:— +VIETNAM +. +Khanh Hoa Province +: +Khanh Vinh District +, +Khanh Trung Commune +, +Suoi Ca Village +, + +400 m + +, + +21 May 2007 + +, + +N +. +Q + + +. + + +Dung +2003 + +( +holotype +: +FIPI +!, isotype: +NY +!) + +. + + + + +PLATE 2. +Left. + +Daemonorops brevicaulis + +—habit. Right. + +Daemonorops ocreata +— + +fruits. + + + + +Stems solitary, non-climbing, free-standing, green, to +0.5 m +long, +3 cm +in diameter without sheaths. Leaves 7; sheaths brownish-green, open, with scattered, yellowish spines to +11 cm +long; ocreas to +4 cm +long, not spiny; knees absent; petioles to +60 cm +long, spiny as the sheaths; rachis to +310 cm +long, with scattered, solitary spines abaxially to +3.5 cm +long; cirri absent; pinnae to 34 per side of rachis, to +51.5 cm +long, +4 cm +wide at the middle, linear–lanceolate, regularly arranged, spreading in the same plane, without bristles. Staminate inflorescences to +1.2 m +long, erect, not flagellate, branched to 2 orders, with to 20 partial inflorescences; prophylls not seen; partial inflorescence bracts tubular, splitting laterally and early deciduous, without spines or the distal ones with few spines; rachillae 1–13 per partial inflorescence, +0.5–2 cm +long; rachillae bracts +6 mm +high; floral bracteoles cupular; staminate flowers +7 mm +long; calyx cupular, +3 mm +long, briefly 3–lobed; corolla +6 mm +long, split to the base into 3 valvate petals; stamens 6; filaments +2.5 mm +long, inflexed at their apices for +0.5 mm +; pistillodes well–developed, +1.5 mm +long; pistillate inflorescences shorter than the staminate, branched to 1 order, with 3 partial inflorescences; prophylls not seen; partial inflorescence bracts tubular, splitting laterally and becoming deciduous, without spines on outer surfaces; rachilla 1 per partial inflorescence, +4–10 cm +long; pistillate flowers +11 mm +long; calyx +6 mm +long, cupular, briefly 3-lobed at the apex; corolla +10 mm +long, tubular below for +3 mm +, free above into 3, valvate petals; staminodes 6, well–developed; fruits ellipsoid, brown, +3.5 cm +long, +2.5 cm +in diameter. + + + + +Distribution and habitat: +—Endemic to southern +Vietnam +in +Khanh Hoa Province +in primary evergreen forest at +400 m +elevation. + + + + +Local names and uses:— +may dat +. No uses recorded. + + + + +Discussion: +— + +Daemonorops brevicaulis + +(named for its short stems) belongs to section + +Piptospatha + +of + +Daemonorops + +, which in +Vietnam +includes all species except +D. jenkinsiana +. It differs from these in a combination of its non–climbing habit, lack of cirri, unbranched partial pistillate inflorescences, and larger fruits. + + + + \ No newline at end of file diff --git a/data/38/7A/C2/387AC21DFFB41872FF16FD424439C07C.xml b/data/38/7A/C2/387AC21DFFB41872FF16FD424439C07C.xml new file mode 100644 index 00000000000..b5762081cfa --- /dev/null +++ b/data/38/7A/C2/387AC21DFFB41872FF16FD424439C07C.xml @@ -0,0 +1,215 @@ + + + +Notes on rattans (Arecaceae) from Vietnam + + + +Author + +Henderson, Andrew +Institute of Systematic Botany, The New York Botanical Garden, Bronx, NY 10458 - 5126, U. S. A. E-mail: ahenderson @ nybg. org Forest Inventory and Planning Institute, Thanh Tri, Hanoi, Vietnam E-mail: dungfipi @ gmail. com + + + +Author + +Dung, Nguyen Quoc + +text + + +Phytotaxa + + +2010 + +2010-08-31 + + +8 + + +25 +33 + + + +journal article +6328 +10.11646/phytotaxa.8.1.2 +ccbf0321-20dc-4799-8575-3f018b87afcc +1179-3163 +4893981 + + + + + + + +Daemonorops ocreata +A.J.Hend. & N.Q.Dung + +, + +sp. nov. + + +( +Plate 2 +) + + + + + + +A speciebus aliis +Daemonorops ocreis prominentibus +et pinnis sin setosis differt. + + + + + + +Type +:— +VIETNAM +. +Khanh Hoa Province +: +Khanh Vinh District +, +Khanh Trung Commune +, +Suoi Ca Village +, + +400 m + +, + +21 May 2007 + +, + +N +. +Q + + +. + + +Dung +2006 + +( +holotype +: +FIPI +!, isotype: +NY +!) + +. + + + + +Stems clustered, climbing, to +12 m +long, +3.2 cm +diam. with sheaths. Leaf sheaths closed, brown with early deciduous whitish tomentum, densely covered with yellowish–brown spines to +6.5 cm +long, interspersed with many smaller spines; ocreas to +10 cm +long, brown, with fewer spines, these distally only; knees present, obscured by spines; petioles to +60 cm +long, spiny on all sides; rachis to +190 cm +long, with scattered, recurved spines abaxially; cirri present, to +70 cm +long; pinnae ca. 34 per side of rachis, the middle ones to +44 cm +long, +2.5 cm +wide at the middle, linear, regularly arranged, spreading in the same plane, bristly along the margins. Staminate inflorescences to +55 cm +long, erect, branched to 2 orders, with 7 partial inflorescences; prophylls to +18 cm +long, covered with rows of yellowish spines; partial inflorescence bracts tubular, without spines, splitting laterally and falling; rachillae 3–5 per partial inflorescence, +2–4 cm +long; staminate flowers not seen; pistillate inflorescences ca. +30 cm +long, erect, branched to 3 orders, with 5–6 partial inflorescences; prophylls to +17 cm +long, covered with rows of yellowish spines; partial inflorescence bracts tubular, splitting laterally, not spiny; rachillae 1–3 per partial inflorescence, +1.5–2.5 cm +long, subtended by shallowly cupular bracts with +3–4 mm +long apiculate margins; pistillate flowers not seen; fruits globose, yellowish, ca. +1.7 cm +diam., the scales deeply channeled; endosperm ruminate. + + + + +Distribution and habitat: +—Endemic to southern +Vietnam +in +Khanh Hoa Province +, in primary evergreen forest at +400–500 m +elevation. + + + + +Local names and uses:— +may gia. +The stems are collected and reported to be of the same, medium quality as + +Daemonorops poilanei + +. + + + + +Discussion: +— + +Daemonorops ocreata + +(named for its conspicuous ocreas) also belongs to section + +Piptospatha + +of + +Daemonorops + +. It differs from + +D. fissilis + +in its much larger size; from + +D. nuichuaensis + +in its climbing habit; from +D. mollispina +in its conspicuous ocreas, lack of woolly indumentum on the leaf sheath spines, lack of bristles on the adaxial pinnae surfaces, and lack of conspicuous bracts subtending the pistillate rachillae; and from + +D. poilanei + +in its conspicuous ocreas, lack of bristles on the adaxial pinnae surfaces, and short, straight pistillate rachillae. + + + + \ No newline at end of file diff --git a/data/38/7A/C2/387AC21DFFB51870FF16FE3844C5C51B.xml b/data/38/7A/C2/387AC21DFFB51870FF16FE3844C5C51B.xml new file mode 100644 index 00000000000..231dd05af93 --- /dev/null +++ b/data/38/7A/C2/387AC21DFFB51870FF16FE3844C5C51B.xml @@ -0,0 +1,209 @@ + + + +Notes on rattans (Arecaceae) from Vietnam + + + +Author + +Henderson, Andrew +Institute of Systematic Botany, The New York Botanical Garden, Bronx, NY 10458 - 5126, U. S. A. E-mail: ahenderson @ nybg. org Forest Inventory and Planning Institute, Thanh Tri, Hanoi, Vietnam E-mail: dungfipi @ gmail. com + + + +Author + +Dung, Nguyen Quoc + +text + + +Phytotaxa + + +2010 + +2010-08-31 + + +8 + + +25 +33 + + + +journal article +6328 +10.11646/phytotaxa.8.1.2 +ccbf0321-20dc-4799-8575-3f018b87afcc +1179-3163 +4893981 + + + + + + + +Calamus parvulus +A.J.Hend. & N.Q.Dung + +, + + +sp. nov +. + +( +Plate 3 +) + + + + + + +A Calamo tetradactylo +ocreis +brevibus, pinnis duos sine setosis, differt. + + + + + + +Type +:— +VIETNAM +. +Khanh Hoa Province +: +Khanh Vinh District +, +Khanh Trung Commune +, +Suoi Ca Village +, + +300–400 m + +, + +21 May 2007 + +, + +N.Q. Dung +2005 + +( +holotype +: +FIPI +!, isotype: NY!) + +. + + + + +PLATE 3. +Left. + +Calamus parvulus +— + +leaves and flagella. Right. + +Calamus seriatus + +—leaf sheath spines, longer at sheath apices. + + + + +Stems clustered, climbing, to +10 m +long, +3 mm +diam. with sheaths. Leaf sheaths green with scattered brown tomentum, with few, recurved, black-tipped spines to +2 mm +long; ocreas scarcely developed, to +3 mm +long; knees present; flagella present, to +55 cm +long; petioles +2.5–3 cm +long, spiny abaxially as the sheaths; rachis +14–19 cm +long, with scattered, solitary or paired spines abaxially; cirri absent; pinnae 2 per side of rachis, the basal ones +11.5–14 cm +long, +1.7–2 cm +wide at the middle, linear-lanceolate, without bristles on veins or margins, the apical ones joined proximally for ca. one third their length. Staminate inflorescences to +0.4 m +long, arching, flagellate, branched to 2 orders, with 3–4 partial inflorescences; prophylls +7–9 cm +long; partial inflorescence bracts tubular, briefly splitting at the apices, with scattered, recurved spines; rachillae 3– 11 per partial inflorescence, +0.5–2 cm +long; staminate flowers +1.5 mm +long (immature); calyx +1 mm +long, deeply split; corolla +1 mm +long, split almost to the base; pistillate inflorescences to +0.25 m +long, arching, not flagellate, branched to 2 orders, with 2 partial inflorescences; rachillae 3–6, to +1 cm +long; pistillate flowers and fruits not seen. + + + + +Distribution and habitat: + +Endemic to southern +Vietnam +in +Khanh Hoa Province +, in primary, evergreen forest at +300–400 m +elevation. + + + + +Local names and uses:— +may chi +. The stems are used in basketry. + + + + +Discussion: +— + +Calamus parvulus + +(named for its small size) differs from all other + +Calamus + +in +Vietnam +by its extremely slender stems, and leaves with only two pinnae per side of the rachis. It appears most similar to + +C. tetradactylus +Hance (1875: 289) + +from which it differs in its more slender stems (3 versus +10 mm +), scarcely developed ocreas (versus well–developed), fewer pinnae per side of the rachis (2 versus 8–13), and pinnae without bristles (versus bristly along the margins). + + + + \ No newline at end of file diff --git a/data/38/7A/C2/387AC21DFFB51873FF16FF0946D2C663.xml b/data/38/7A/C2/387AC21DFFB51873FF16FF0946D2C663.xml new file mode 100644 index 00000000000..02d1c52e4e4 --- /dev/null +++ b/data/38/7A/C2/387AC21DFFB51873FF16FF0946D2C663.xml @@ -0,0 +1,80 @@ + + + +Notes on rattans (Arecaceae) from Vietnam + + + +Author + +Henderson, Andrew +Institute of Systematic Botany, The New York Botanical Garden, Bronx, NY 10458 - 5126, U. S. A. E-mail: ahenderson @ nybg. org Forest Inventory and Planning Institute, Thanh Tri, Hanoi, Vietnam E-mail: dungfipi @ gmail. com + + + +Author + +Dung, Nguyen Quoc + +text + + +Phytotaxa + + +2010 + +2010-08-31 + + +8 + + +25 +33 + + + +journal article +6328 +10.11646/phytotaxa.8.1.2 +ccbf0321-20dc-4799-8575-3f018b87afcc +1179-3163 +4893981 + + + + + + +Calamus +Linnaeus (1753: 325) + + + + + + +With the transfer of + +Calamus fissilis + +and + +C. nuichuaensis + +to + +Daemonorops + +(see above), there are now 30 currently recognized species of + +Calamus + +in +Vietnam +. Recent field work has revealed the following three new species. + + + + \ No newline at end of file diff --git a/data/38/7A/C2/387AC21DFFB61870FF16FD104353C1A1.xml b/data/38/7A/C2/387AC21DFFB61870FF16FD104353C1A1.xml new file mode 100644 index 00000000000..5b0547884f1 --- /dev/null +++ b/data/38/7A/C2/387AC21DFFB61870FF16FD104353C1A1.xml @@ -0,0 +1,194 @@ + + + +Notes on rattans (Arecaceae) from Vietnam + + + +Author + +Henderson, Andrew +Institute of Systematic Botany, The New York Botanical Garden, Bronx, NY 10458 - 5126, U. S. A. E-mail: ahenderson @ nybg. org Forest Inventory and Planning Institute, Thanh Tri, Hanoi, Vietnam E-mail: dungfipi @ gmail. com + + + +Author + +Dung, Nguyen Quoc + +text + + +Phytotaxa + + +2010 + +2010-08-31 + + +8 + + +25 +33 + + + +journal article +6328 +10.11646/phytotaxa.8.1.2 +ccbf0321-20dc-4799-8575-3f018b87afcc +1179-3163 +4893981 + + + + + + + +Calamus seriatus +A.J.Hend. & N.Q.Dung + +, + +sp. nov. + + +( +Plate 3 +) + + + + + + +A speciebus similibus ( +Calamus flagellum +, +C. guruba +, +C. rhabdocladus +, +C. rudentum +) pinnis 8–9 aggretatis in duo catervas distantes differt. + + + + + + +Type +:— +VIETNAM +. +Khanh Hoa Province +: +Khanh Vinh District +, +Khanh Trung Commune +, +Suoi Ca Village +, + +300–400 m + +, + +21 May 2007 + +, + +N.Q. Dung +2004 + +( +holotype +: +FIPI +!, isotype: NY!) + +. + + + + +Stems clustered, climbing, to +10 m +long, +1.8 cm +diam. with sheaths. Leaf sheaths closed, green with brown tomentum, densely covered with yellowish spines to +1.5 cm +long, those at the sheath apices longer, to +4 cm +long, forming rows on either side of sheath apices and petiole bases; ocreas scarcely developed; knees absent; flagella present, to +60 cm +long; petioles to +30 cm +long, spiny laterally and abaxially as the sheaths; rachis to +42 cm +long, with scattered, solitary, recurved spines abaxially; cirri absent; pinnae 8–9 per side of rachis, +29–35 cm +long, +2–3 cm +wide at the middle, linear–lanceolate, arranged in two distant groups of 5 pinnae distally and 3–4 proximally, scarcely bristly along the margins, the apical pair of pinnae joined distally for one third to one half their length. Staminate inflorescences to +0.7 m +long, arching, flagellate, branched to 2 orders, with 4 partial inflorescences; prophylls not seen; partial inflorescence bracts tubular, briefly splitting at the apices, without spines; rachillae 5–6 per partial inflorescence, +2–5 cm +long; staminate flowers not seen; pistillate inflorescences not seen; fruits not seen. + + + + +Distribution and habitat: +—Endemic to southern +Vietnam +in +Khanh Hoa Province +in primary, evergreen forest at +300–400 m +elevation. + + + + +Local names and uses: +— +may cam +. The stems are used in basketry. + + + + +Discussion: +— + +Calamus seriatus + +(named for its rows of spines at sheath apices) appears most similar to that group of species having the leaf sheath spines conspicuously longer at the sheath apices ( + +C. flagellum +Griffith ex Martius (1853: 333) + +, + +C. guruba +Buchanan-Hamilton + +in Martius (1838: 211), + +C. rhabdocladus +Burret (1930: 884) + +and + +C. rudentum +Loureiro (1790: 209)) + +. It differs from all these in its 8–9 pinnae per side of the rachis arranged in two distant groups with the apical pair joined at their bases, versus 27–65 pinnae per side of the rachis arranged regularly or sometimes irregularly with the apical pair not joined at their bases. + + + + \ No newline at end of file diff --git a/data/38/7A/C2/387AC21DFFB6187EFF16F9794491C6B5.xml b/data/38/7A/C2/387AC21DFFB6187EFF16F9794491C6B5.xml new file mode 100644 index 00000000000..fe718a2e9c0 --- /dev/null +++ b/data/38/7A/C2/387AC21DFFB6187EFF16F9794491C6B5.xml @@ -0,0 +1,250 @@ + + + +Notes on rattans (Arecaceae) from Vietnam + + + +Author + +Henderson, Andrew +Institute of Systematic Botany, The New York Botanical Garden, Bronx, NY 10458 - 5126, U. S. A. E-mail: ahenderson @ nybg. org Forest Inventory and Planning Institute, Thanh Tri, Hanoi, Vietnam E-mail: dungfipi @ gmail. com + + + +Author + +Dung, Nguyen Quoc + +text + + +Phytotaxa + + +2010 + +2010-08-31 + + +8 + + +25 +33 + + + +journal article +6328 +10.11646/phytotaxa.8.1.2 +ccbf0321-20dc-4799-8575-3f018b87afcc +1179-3163 +4893981 + + + + + + + +Calamus yentuensis +A.J.Hend. & N.Q.Dung + +, + +sp. nov. + + +( +Plate 4 +) + + + + + + +A speciebus aliis Calami +habitu +non scandenti, +ocreis +prominentibus, pinnis aggregatis, et inflorescentiae flagelliformis differt. + + + + + + +Type +:— +VIETNAM +. +Quang Ninh Province +: +Dong Trieu District +, +Yen Tu Mountain +, pagoda area, +21.11°N +, +106.72°E +, ca. + +100 m + +, + +7 June 2009 + +, + +A. Henderson +& +N.Q. Dung +3601 + +( +holotype +: +FIPI +!, isotype: NY!) + +. + + + + +PLATE 4. + +Calamus yentuensis + +. Left. Habit. Right. Leaf sheaths showing ocreas. + + + + +Stems clustered, non-climbing, free-standing, green, to +1.5 m +long, +1.2 cm +in diameter without sheaths; internodes +2.5 cm +long. Leaves 10–12; sheaths open, with rings of black spines to +4.5 cm +long, interspersed among many smaller spines; ocreas to +15 cm +long, covered with rings of spines as the sheaths, with a tuft of brownish hairs at the apices, becoming split into two ‘ears’; knees absent; flagella absent; petioles to +50 cm +long, spiny on all sides as the sheaths; rachis +50–70 cm +long, with scattered, solitary spines abaxially; cirri absent; pinnae ca. 43 per side of rachis, +11–25 cm +long, +0.5–1 cm +wide at the middle, linear, regularly arranged but with gaps, spreading in the same plane, pendulous at the apices, bristly on main veins and lateral veins adaxially and abaxially and along the margins. Staminate inflorescences to +3 m +long, arching, flagellate, branched to 3 orders, with 3 partial inflorescences; prophylls not seen; partial inflorescence bracts tubular, briefly splitting at the apices, without spines; rachillae +1 cm +long; rachillae bracts +2 mm +high, cupular; floral bracteoles cupular; staminate flowers +3.7–4 mm +long; calyx tubular, +2–2.2 mm +long, briefly 3-lobed; corolla +3–3.3 mm +long, split almost to the base into 3 valvate petals; stamens 6; filaments inflexed at the apices; pistillodes well–developed, +2.5 mm +long; pistillate inflorescences to +3 m +long, arching, flagellate, branched to 2 orders, with 3 partial inflorescences; prophylls not seen; partial inflorescence bracts tubular, splitting laterally, with some recurved spines on outer surfaces; rachillae +8–9 cm +long; rachillae bracts +2.5 cm +long; floral bracteoles cupular; pistillate flowers +4.5 mm +long; calyx +4 mm +long, briefly 3-lobed at the apex; corolla +3 mm +long, briefly 3-lobed at the apex; staminodes well–developed; fruits globose, brown, ca. +1 cm +in diameter; endosperm homogeneous. + + + + +Distribution and habitat: + +Endemic to northern +Vietnam +in +Quang Ninh Province +on Yen Tu Mountain, in disturbed forest at the base of the mountain. + + + + +Local names and uses:— +may den. +The stems are used in furniture making. + + + + + +Additional specimen examined ( +paratype +):— + + +VIETNAM +. +Quang Ninh Province +: +Dong Trieu District +, +Yen Tu Mountain +, pagoda area, +21.11°N +, +106.72°E +, ca. + +100 m + +, + +7 June 2009 + +, + +A. Henderson +& +N.Q. Dung +3602 + +( +FIPI +, NY) + +. + + + + +Discussion: +—This unusual species differs from all other non–climbing + +Calamus + +in +Vietnam +and adjacent +China +, by its elaborate ocreas, interruptedly pinnate leaves, and elongate, flagellate inflorescences. It is named for Yen Tu Mountain, its only known locality. + + + + \ No newline at end of file diff --git a/data/38/7B/25/387B25F968905EEEA2B3C64D70C478A0.xml b/data/38/7B/25/387B25F968905EEEA2B3C64D70C478A0.xml new file mode 100644 index 00000000000..60cae7f391e --- /dev/null +++ b/data/38/7B/25/387B25F968905EEEA2B3C64D70C478A0.xml @@ -0,0 +1,421 @@ + + + +Hedysarum qilianshanense sp. nov. (Fabaceae, Hedysareae), a new species from the Qilianshan Mountains in Gansu, China + + + +Author + +Liu, Pei-Liang +https://orcid.org/0000-0001-6566-7824 +Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Northwest University, Xi'an, Shaanxi 710069, China + + + +Author + +Guo, Qian-Xi +https://orcid.org/0009-0002-9144-5752 +Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Northwest University, Xi'an, Shaanxi 710069, China + + + +Author + +Zhang, Jian-Qi +Linhai City Natural Resources and Planning Bureau of Zhejiang Province, Linhai, Zhejiang 317099, China + + + +Author + +Xun, Lu-Lu +https://orcid.org/0000-0002-6861-5883 +Shaanxi Engineering Research Centre for Conservation and Utilization of Botanical Resources, Xi'an Botanical Garden of Shaanxi Province (Institute of Botany of Shaanxi Province), Xi'an, Shaanxi 710061, China + + + +Author + +Lu, Yuan +https://orcid.org/0000-0002-0329-0803 +Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Northwest University, Xi'an, Shaanxi 710069, China & Shaanxi Engineering Research Centre for Conservation and Utilization of Botanical Resources, Xi'an Botanical Garden of Shaanxi Province (Institute of Botany of Shaanxi Province), Xi'an, Shaanxi 710061, China + + + +Author + +Yue, Ming +https://orcid.org/0000-0002-8618-1126 +Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Northwest University, Xi'an, Shaanxi 710069, China & Shaanxi Engineering Research Centre for Conservation and Utilization of Botanical Resources, Xi'an Botanical Garden of Shaanxi Province (Institute of Botany of Shaanxi Province), Xi'an, Shaanxi 710061, China +yueming@nwu.edu.cn + +text + + +PhytoKeys + + +2024 + +2024-01-22 + + +237 + + +103 +116 + + + + +http://dx.doi.org/10.3897/phytokeys.237.116236 + +journal article +http://dx.doi.org/10.3897/phytokeys.237.116236 +1314-2003-237-103 +FF3A7EF9A1EB55F4B35DD922853A17FE + + + + +Hedysarum qilianshanense P.L.Liu, sp. nov. (H. sect. Hedysarum) + + + + +Figs 3 +, 4 + + + + +Type +. + + + +China +, +Gansu Province +, + +Su'nan +County + +, the +Heihe River valley +, +Xiaogushan +, in crevice on stony slope, + +2053 m +above sea level + +(a. s. l.), +38°41′6.38″N +, +110°3′9.98″E +, +21 June 2019 +, + +P. L. Liu +458 + +( +Holotype +, WUK!, barcode WUK0536471; +Isotypes +, WUK!, barcodes WUK0536466-WUK0536470, WNU!) + +. + + + +Diagnosis. + +This new species is morphologically similar to + +H. przewalskii + +, but can be distinguished by its light purple to purple corolla (vs. light yellow to yellow corolla), 15-19 mm long standard (vs. 10-14 mm long standard), 14-16 mm long wings (vs. 10-14 mm long wings), 16-19 mm long keels (vs. 12-17 mm long keels), and glabrous ovaries and legumes (vs. often pubescent, sometimes glabrate or glabrous ovaries and legumes). The new species can be easily distinguished from + +H. neglectum + +by its bract shorter than pedicel (vs. bract longer than pedicel), and glabrous ovaries and legumes (vs. pubescent ovaries and legumes) (Table +2 +). + + + +Figure 3. +Illustration of + +Hedysarum qilianshanense + +a +root and basal part of stems +b +upper part of plant +c +calyx tube (split between an adaxial tooth and a lateral tooth) +d +bracteoles +e +standard +f +wing +g +keel +h +androecium +i +pistil +j +infructescence +k +legume. Drawn by Xiu-Zhen Wu. + + + + +Table 2. +Morphological comparison of + +Hedysarum qilianshanense + +, + +H. przewalskii + +and + +H. neglectum + +. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
- + +H. qilianshanense + + + +H. przewalskii + + + +H. neglectum + +
Bractshorter than pedicelshorter than pedicellonger than pedicel
Corolla colorlight purple to purplelight yellow to yellowpurple
Standard length15-19 mm10-14 mm13-14 mm
Wing length14-16 mm10-14 mm13-14 mm
Keel length16-19 mm12-17 mm15-16 mm
Ovary and legumeglabrousoften pubescent, sometimes glabrate or glabrouspubescent
+
+
+ +Description. + +Perennial herbs, 30-100 cm tall. Main root stout, woody, up to 1.3 cm in diameter. Stems cespitose, ascending, branched; internodes glabrous or loosely pubescent, nodes pubescent. Leaves imparipinnate, alternate, 12-30 cm long; stipules connate, opposite to leaves, wide triangular, membranous, brown, glabrous, apex shallowly bilobed, lower ones 8-17 mm long, becoming smaller in upper part of stem; rachises sulcate, glabrous or sparsely pubescent; leaflets 9-19, opposite or alternate; petiolules ca. 1 mm long, pubescent; leaflet blades elliptic, ovate-elliptic, oblong, 12-40 +x +7-25 mm, adaxial surface glabrous, abaxial surface sparsely pubescent along midvein, base wide cuneate or rounded, apex obtuse, rounded or retuse. Racemes axillary, exceeding leaves, 15-42 cm long, with 15-50 flowers, peduncles pubescent; pedicel 3-6 mm long, pubescent; bracts linear, with brown midvein, pubescent, 2-5 mm long; bracteoles 2, linear, with brown midvein, pubescent, 2-3.5 mm long; calyx tube campanulate, 3-4 mm long, pubescent; calyx teeth 5, pubescent, the two adaxial teeth triangular, ca. 1 mm long, the two lateral teeth narrowly triangular, 1.5-2.5 mm long, the abaxial tooth linear-triangular, 2-3 mm long; corolla light purple to purple; standard obovate, 15-19 +x +5.5-7 mm, apex retuse, base attenuate; wings 14-16 +x +2-2.5 mm, auricle linear, as long as claw, 2-3 mm long; keels 16-19 +x +4-5 mm, auricle triangular, ca. 1 mm long; androecium diadelphous, 12-17 mm long; ovary linear, glabrous, style ca. 13 mm long. Legume a loment, divided into 2-4 articles, with a small beak at apex; articles elliptic, compressed, 8-10 mm +x +6-7 mm, glabrous, with reticulate veins, with a narrow wing ca. 0.5 mm wide along the dorsal suture only. Seed reniform, yellow, ca. 3 +x +2 mm. + + + +Figure 4. +Photos of + +Hedysarum qilianshanense + +from the field +A +habitat +B +plant +C +raceme +D +infructescence. Photographed by Pei-Liang Liu. + + + + +Phenology. +Flowering and fruiting in June. + + +Distribution and habitat. + + +Hedysarum qilianshanense + +is only known from +Su'nan +, Gansu, China. It grows in stony slope and forest edge in valley, 2053-3000 m a. s. l. + + + +Etymology. + +The epithet + +Hedysarum qilianshanense + +is transliterated from the type location, Qilianshan Mountains in China. The Chinese vernacular name for this new species is +祁连山岩黄耆 +( +qi +lian +shan +yan +huang +qi +). + + + + +Other specimens examined +( +Paratypes +). + + + +China +, +Gansu Province +, + +Su'nan +County + +, +Sidalong +, + +Wulin'gou + +, on stony slope, + +3000 m +a. s. l. + +, +21 June 1986 +, + +Sheng Huan Bao Dui +86055 + +(NWTC!); + +Su'nan +County + +, +Sidalong +, + +Wulin'gou + +, in crevice on stony slope, + +2542 m +a. s. l. + +, +38°28′1.67″N +, +99°56′54.63″E +, +21 June 2019 +, + +P. L. Liu +461 + +(WUK!, barcodes WUK0536462, WUK0536463, WNU!); + +Su'nan +County + +, +Sidalong +, on slope on forest edge, + +2632 m +a. s. l. + +, +38°27′26.6″N +, +99°54′52.69″E +, +21 June 2019 +, + +P. L. Liu +470 + +(WUK!, barcodes WUK0536464, WUK0536465, WNU!) + +. + + +
+
\ No newline at end of file diff --git a/data/38/7B/27/387B27072503BACC1B4B343C154ACE29.xml b/data/38/7B/27/387B27072503BACC1B4B343C154ACE29.xml new file mode 100644 index 00000000000..e6247daecc0 --- /dev/null +++ b/data/38/7B/27/387B27072503BACC1B4B343C154ACE29.xml @@ -0,0 +1,95 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part L) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +610 +650 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Lagerstroemia indica +Linnaeus + +, + +Systema Naturae +, ed. 10, 2 + +: 1076. 1759 + + +. + + + +["Habitat in China."] Sp. Pl., ed. 2, 1: 734. 1762. RCN: 3881. + + + +Lectotype +(Merrill, +Interpret. Rumph. Herb. Amb. +: 381. 1917): [icon] " + +Tsjinkin + +" in Rumphius, Herb. Amboin. Auct.: 61, t. 28, f. 1. 1755. + + + + +Generitype +of + +Lagerstroemia +Linnaeus. + + + + + +Current name: + +Lagerstroemia indica +L. + +( +Lythraceae +). + + + + \ No newline at end of file diff --git a/data/38/7B/48/387B48D2919F2197B6B7028B2277CBEE.xml b/data/38/7B/48/387B48D2919F2197B6B7028B2277CBEE.xml new file mode 100644 index 00000000000..b328d78e8b7 --- /dev/null +++ b/data/38/7B/48/387B48D2919F2197B6B7028B2277CBEE.xml @@ -0,0 +1,65 @@ + + + +Order Rodentia - Family Sciuridae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 2 + + + +754 +818 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316535 + + + + + +Tamias (Eutamias) sibiricus +subsp. +ordinalis +Thomas 1908 + + + + + +Synonyms: + +Tamias (Eutamias) sibiricus +subsp. +albogularis +(J. A. Allen 1909) + +. + + + + \ No newline at end of file diff --git a/data/38/7B/80/387B80E84BE04B5AD16157F7394C39E3.xml b/data/38/7B/80/387B80E84BE04B5AD16157F7394C39E3.xml new file mode 100644 index 00000000000..7fac7cd67ca --- /dev/null +++ b/data/38/7B/80/387B80E84BE04B5AD16157F7394C39E3.xml @@ -0,0 +1,172 @@ + + + +North-Western Palaearctic species of the Pristiphora ruficornis group (Hymenoptera, Tenthredinidae) + + + +Author + +Prous, Marko +https://orcid.org/0000-0002-5329-7608 +Senckenberg Deutsches Entomologisches Institut, Eberswalder Strasse 90, 15374 Muencheberg, Germany & Department of Zoology, Institute of Ecology and Earth Sciences, University of Tartu, Vanemuise 46, 51014 Tartu, Estonia +mprous@ut.ee + + + +Author + +Vikberg, Veli +Liinalammintie 11 as. 6, FI- 14200 Turenki, Finland + + + +Author + +Liston, Andrew +Senckenberg Deutsches Entomologisches Institut, Eberswalder Strasse 90, 15374 Muencheberg, Germany + + + +Author + +Kramp, Katja +Senckenberg Deutsches Entomologisches Institut, Eberswalder Strasse 90, 15374 Muencheberg, Germany + +text + + +Journal of Hymenoptera Research + + +2016 + +2016-08-29 + + +51 + + +1 +54 + + + + +http://dx.doi.org/10.3897/jhr.51.9162 + +journal article +http://dx.doi.org/10.3897/jhr.51.9162 +1314-2607-51-1 +B3D68EDB9CF844A3BC43E9C2D6626BD7 +FFCF966B691BFFC1FF950C14486D5B5D +147922 + + + + + +Pristiphora +sootryeni Lindqvist, 1955 + + + + + +Pristiphora sootryeni +Lindqvist, 1955: 46. Holotype ♀ in TROM, not examined. Type locality: +Smastroemmen +, Finnmark, Norway. + + + +Similar species. + +Based on the external morphology, the most similar species are + +P. astragali + +, + +P. confusa + +, + +P. opaca + +, + +P. pusilla + +, + +P. staudingeri + +, and + +P. subopaca + +, from which it is +best +distinguished by the structure of the lancet (Fig. +45 +). The lancet has weak ctenidia (weak or well-developed in the others) and on the inner surface of the lancet there are small spiny pectines (or dentes semicirculares) that reach the sclerora (present also in + +P. astragali + +). However, differences from + +P. astragali + +are rather small. Morphologically, the subapical tooth of the claws tends to be larger, the apical serrulae of the lancet are longer, and the number of ctenidia on the lancet is larger than in + +P. astragali + +(Figs +43-44 +; +Vikberg 2006 +). Male unknown. + + + +Genetic data. + +Based on a COI barcode sequence of one confidently identified specimen from Kuusamo (Finland; DEI-GISHym80036), it belongs to the same BIN cluster as + +P. astragali + +(BOLD:AAL8292), which in the BOLD database includes two other unidentified specimens from Manitoba, Canada (Fig. +1 +). The nearest neighbour (BOLD:AAL8277) is 2.40% different. BIN cluster BOLD:AAL8277 might include + +P. astragali + +, as one of the included specimens in BOLD database was identified by Matti Viitasaari as " +Pristiphora nr. astragali +". Amplification of TPI failed. + + + +Host plants. + + +Oxytropis campestris + +(L.) DC. ( +Lindqvist 1973 +; +Vikberg 2006 +). + + + +Distribution and material examined. + +Western Palaearctic. Specimens studied are from +Finland +. + + + + \ No newline at end of file diff --git a/data/38/7B/8E/387B8EAEAB4AC0BEBFA5E2CDCC61456D.xml b/data/38/7B/8E/387B8EAEAB4AC0BEBFA5E2CDCC61456D.xml new file mode 100644 index 00000000000..8528f05170e --- /dev/null +++ b/data/38/7B/8E/387B8EAEAB4AC0BEBFA5E2CDCC61456D.xml @@ -0,0 +1,76 @@ + + + +Taxonomy of Afrotropical and West Palaearctic ants of the ponerine genus Hypoponera Santschi (Hymenoptera: Formicidae). + + + +Author + +Bolton, B. + + + +Author + +Fisher, B. L. + +text + + +Zootaxa + + +2011 + +2843 + + +1 +118 + + + + +http://antbase.org/ants/publications/23490/23490.pdf + +journal article +23490 + + + + +boerorum +group + + + +Species with the following combination of characters in the worker caste. +1 Metanotal groove present across dorsum of mesosoma. +2 Petiole node not squamiform. +3 Eyes usually present, rarely absent. +4 Maximum width of first gastral tergite in dorsal view is about the same as the width of the second tergite at its midlength. +5 Cinctus of second gastral tergite with strong cross-ribs. + + + +6 Anterior clypeal margin lacks a median indentation or notch. Five southern African species are included here ( +boerorum +, +ignavia +, +spei +, +sulcatinasis +, +transvaalensis +). The + + +group may be artificial as it basically represents species that are similar to the +abeillei +group but which retain a strongly developed metanotal groove. + + + + \ No newline at end of file diff --git a/data/38/7B/BA/387BBAFDCA153C2BE3674E3C4026349B.xml b/data/38/7B/BA/387BBAFDCA153C2BE3674E3C4026349B.xml new file mode 100644 index 00000000000..945f1350c63 --- /dev/null +++ b/data/38/7B/BA/387BBAFDCA153C2BE3674E3C4026349B.xml @@ -0,0 +1,86 @@ + + + +Order Cingulata + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +94 +99 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Euphractus sexcinctus +subsp. +flavimanus +Desmarest 1804 + + + + + +Synonyms: + +Euphractus sexcinctus +subsp. +encoubert +(Desmarest 1822) + +; + +Euphractus sexcinctus +subsp. +flavipes +(G. Fischer 1814) + +; + +Euphractus sexcinctus +subsp. +gilvipes +(Lichtenstein 1818) + +; + +Euphractus sexcinctus +subsp. +poyu +(Larrañaga 1923) + +. + + + + \ No newline at end of file diff --git a/data/38/7B/CB/387BCBF508AB255C5A7536D2ABA6660E.xml b/data/38/7B/CB/387BCBF508AB255C5A7536D2ABA6660E.xml new file mode 100644 index 00000000000..4e10786aca5 --- /dev/null +++ b/data/38/7B/CB/387BCBF508AB255C5A7536D2ABA6660E.xml @@ -0,0 +1,90 @@ + + + +Revision of the genera Hovadelium Ardoin and Mimolaena Ardoin (Coleoptera, Tenebrionidae, Laenini) from Madagascar, with remarks on tribal assignment 1 + + + +Author + +Schawaller, Wolfgang + +text + + +ZooKeys + + +2013 + +326 + + +55 +67 + + + + +http://dx.doi.org/10.3897/zookeys.326.5871 + +journal article +http://dx.doi.org/10.3897/zookeys.326.5871 +1313-2970-326-55 + + + + +Mimolaena janaki +sp. n. +Figs 8, 14 + + + +Type specimens. + +Holotype male: E Madagascar, Ranomafana NP, Vohiparara, 1100-1200 m, 21.-24.I.1993, leg. J. +Janak +, SMNS. - Paratypes: Same data as holotype, 3 ex. SMNS, 2 ex. ZSM. - E Madagascar, Massiv Ambondrombe, 1600-1700 m, 17.III.1996, leg. J. +Janak +& P. Moravec, 1 ♀ SMNS. - E Madagascar, Massiv Ambondrombe, 1500-1600 m, 15.-18.III.1996, leg. J. +Janak +& P. Moravec, 1 ♀ ZSM. - E +Madagascar +, Massiv Ambondrombe, 1300-1400 m, 14.III.1996, leg. J. +Janak +& P. Moravec, 1 ♀ SMNS. + + + +Diagnosis. + +To be recognized by the shape of the pronotum with spine-like posterior angles, by scattered and fine punctation of the pronotum, by only six elytral rows of punctures extinguished in the posterior and external part of elytra, and by the shape of the aedeagus. The two other known species of +Mimolaena +possess nearly rounded posterior angles of the pronotum, and the punctation on the pronotum is either fine and the elytra bear punctural rows ( +Mimolaena pauliani +Ardoin, 1961), or the punctation on the pronotum is rough and dense and the elytra bear an dense irregular punctation not separated in rows and intervals ( +Mimolaena clarissae +Ferrer, 1998). See also key below. + + + +Description. + +Body length 3.5-4.7 mm, unicoloured dark brown. Eyes (Fig. 8) not reduced, slightly prominent. Shape of the antennomeres see Fig. 8. Shape of pronotum see Fig. 8, disc with a few scattered punctures, most punctures bearing a longer erect seta; surface without any impressions, surface shining, lateral margins bordered, basal margin bordered and not bent downwards, posterior angles prominent spine-like, propleura unpunctured. Elytra (Fig. 8) with only six punctural rows without +striae +, these rows extinguishing in posterior and external part of elytra, punctures of rows of similar size as pronotal punctures, punctures of the elytral rows without setae, a few additional punctures apart from the rows laterally and distally on the elytra bear a longer erect seta, intervals shining without any punctures and setation, intervals flat. Ventrites shining, in males with fine punctation and short setation, in females nearly unpunctured and without setation, last ventrite in both sexes unbordered. Femora and tibiae in both sexes without teeth or other modifications. Aedeagus see Fig. 14. + + + +Etymology. + +Named in honor of J. +Janak +, one of the collectors of the type series and of other Malagasy +Laenini +. + + + + \ No newline at end of file diff --git a/data/38/7C/66/387C66F605055A478348C39E111D743D.xml b/data/38/7C/66/387C66F605055A478348C39E111D743D.xml new file mode 100644 index 00000000000..87f2d30c3b1 --- /dev/null +++ b/data/38/7C/66/387C66F605055A478348C39E111D743D.xml @@ -0,0 +1,287 @@ + + + +Taxonomic revision of the new spider genus Hortophora, the Australasian Garden Orb-weavers (Araneae, Araneidae) + + + +Author + +Framenau, Volker W. +https://orcid.org/0000-0002-7724-3831 +Harry Butler Institute, Murdoch University, Murdoch, Western Australia 6150, Australia & Department of Terrestrial Zoology, Western Australian Museum, Welshpool, Western Australia 6103, Australia & Zoological Museum Hamburg, Leibnitz Institute for the Analysis of Biodiversity Change (LIB), Centre for Taxonomy & Morphology, Martin-Luther-King-Platz 3, 20146 Hamburg, Germany +volker.framenau@murdoch.edu.au + + + +Author + +Baptista, Renner L. C. +Laboratorio de Diversidade de Aracnideos, Universidade do Brasil / Universidade Federal do Rio de Janeiro. Av. Carlos Chagas Filho 373, 21941 - 902, Ilha do Fundao, Rio de Janeiro, Brazil + + + +Author + +Oliveira, Francisca Samia M. +Laboratorio de Diversidade de Aracnideos, Universidade do Brasil / Universidade Federal do Rio de Janeiro. Av. Carlos Chagas Filho 373, 21941 - 902, Ilha do Fundao, Rio de Janeiro, Brazil + + + +Author + +Castanheira, Pedro de S. +https://orcid.org/0000-0002-0623-1622 +Harry Butler Institute, Murdoch University, Murdoch, Western Australia 6150, Australia & Laboratorio de Diversidade de Aracnideos, Universidade do Brasil / Universidade Federal do Rio de Janeiro. Av. Carlos Chagas Filho 373, 21941 - 902, Ilha do Fundao, Rio de Janeiro, Brazil + +text + + +Evolutionary Systematics + + +2021 + +2021-11-02 + + +5 + + +2 + + +275 +334 + + + + +http://dx.doi.org/10.3897/evolsyst.5.72474 + +journal article +http://dx.doi.org/10.3897/evolsyst.5.72474 +2535-0730-2-275 +9AC22770F3004265A21F841EA364FFD5 +671FAEEE86B25BE9A720A18193BC42B1 + + + + +Hortophora cucullus Framenau & Castanheira +sp. nov. + + + + +Figs 2B +, 9 +, 10 +, 11 + + + +Type material. + +Holotype +male, Pandappa Conservation Park ( +33°10'00"S +, +139°08'15"E +, South Australia, Australia), 22-25 April 2003, D. Hirst, night collection, mallee and sparse chenopods (SAM NN19582). + + + +Etymology. + +The specific epithet is a masculine noun in apposition from Latin + +Hortophora cucullus + +- a +monk's +hat, and refers to the distinct abdominal shape, specifically of the male of this species. + + + +Other material examined. +See Appendix 1. + + +Diagnosis. + +Males of + +Hortophora cucullus + +sp. nov. can be easily identified from all other + +Hortophora + +species by the lateral lobes on the abdomen of both males (Fig. +9A +) and females (Fig. +10A +), which are absent in all other species. In addition, males (and less so females) differ by the dorsally drawn up abdomen (Fig. +9B +). The male pedipalp + +H. cucullus + +sp. nov. has two macrosetae on the patella (Fig. +9E +), one being smaller, but there is only one in all other + +Hortophora + +gen. nov. species. + + + +Figure 9. + +Hortophora cucullus + +sp. nov., male holotype (SAM NN19582). +A. +dorsal habitus; +B. +lateral habitus; +C. +ventral habitus; +D. +left pedipalp, ventral view; +E. +left pedipalp, dorsal view. Scale bars: 2 mm ( +A-C +); 0.2 mm ( +D, E +). + + + + +Figure 10. + +Hortophora cucullus + +sp. nov., female (WAM T70164). +A. +dorsal habitus; +B. +ventral habitus; +C. +epigyne, ventral view; +D. +epigyne, lateral view; +E. +epigyne, posterior view. Scale bars: 2 mm ( +A, B +); 0.2 mm ( +C-E +). + + + + +Description. + +Male +(holotype, SAM NN19582): Total length 11.5. Carapace 4.1 long, 2.9 wide, dark brown with yellow setae mainly centrally (Fig. +9A +). Eyes diameter AME 0.23, ALE 0.13, PME 0.20, PLE 0.13; row of eyes: AME 0.67, PME 0.61, PLE 1.37. Chelicerae brown; two promarginal teeth and one retromarginal tooth. Legs brown to light brown, femora basally yellow-brown (Fig. +9A-C +). Tibiae of leg II very little enlarged and without strong spines, but distinct white setae ventrally (Figs +2B +, +9A-C +). Leg formula I> IV> II> III; and length of segments (femur + patella + tibia + metatarsus + tarsus = total length): I - 5.0 + 2.6 + 4.7 + 4.0 + 1.6 = 17.9, II - 4.0 + 2.2 + 3.7 + 0.9 + 1.5 = 12.3, III - 2.9 + 1.3 + 2.0 + 1.5 + 0.9 = 8.6, IV - 3.4 + 1.8 + 3.3 + 3.4 + 1.2 = 13.1. Labium 0.36 long, 0.52 wide, brown; endites brown. Sternum 1.9 long, 0.9 wide, dark brown with few yellow setae (Fig. +9C +). Abdomen 7.5 long, 3.5 wide, dorsally extended and arching posteriorly and with lateral protrusions (Fig. +9A-C +); dorsum olive-brown and mottled yellow-brown (Fig. +9A-C +); venter dark olive-brown (Fig. +9C +). Pedipalp length of segments (femur + patella + tibia + cymbium = total length): 0.7 + 0.4 + 0.3 + 1.3 = 2.7; paracymbium short (Fig. +9E +); median apophysis elongate transverse and apically bifid curved tip (Fig. +9D +); conductor lobe large and rectangular, clearly connecting to the conductor basis from beneath the embolus (Fig. +9D +); terminal apophysis bubble-shaped tapering into an elongated, sclerotised tip (Fig. +9D +); conductor with strong sclerotised tip (Fig. +9D, E +); embolus strong and curved apically (Fig. +9D +). + + +Female +(WAM T70164): Total length 13.1. Carapace 6.0 long, 5.2 wide; reddish-brown, cephalic area and lateral flanks darker, flanks covered in with white setae (Fig. +10A +). Eyes diameter AME 0.32, ALE 0.18, PME 0.16, PLE 0.18; row of eyes: AME 0.88, PME 0.79, PLE 2.36. Chelicerae dark reddish-brown; four promarginal teeth (apical and third largest) and two retromarginal teeth (basal largest). Legs orange-brown and mottled in dark brown especially along joints (Fig. +10A, B +). Pedipalp length of segments (femur + patella + tibia + tarsus = total length): 1.3 + 1.0 + 1.1 + 2.0 = 5.4. Leg formula I> IV> II> III; and length of segments: I - 6.2 + 3.6 + 4.8 + 4.1 + 1.5 = 20.2, II - 5.6 + 3.8 + 4.7 + 0.9 + 1.3 = 16.3, III - 4.1 + 2.1 + 2.0 + 2.3 + 1.0 = 11.5, IV - 4.6 + 3.2 + 4.0 + 3.9 + 1.3 = 17.0. Labium 0.94 long, 1.26 wide, dark brown; endites reddish-brown (Fig. +10B +). Sternum 2.7 long, 2.0 wide, dark brown, with white setae particularly along the lateral edges (Fig. +10B +). Abdomen 8.8 long, 8.2 wide, with lateral, dorsal and posterior humps, dorsum dark olive-brown, mottled with yellow spots (Fig. +10A +); venter olive-brown with lateral rows of white spots (Fig. +10B +); Epigyne (Fig. +10C-E +) base ovoid; scape highly elongated and centrally slightly wider, short dorsal narrow ridge in basal half (Fig. +10D, E +), covered with sparse long setae. + + + +Variation. + +Size variation: total length males 11.5-12.1 (n=2), females 13.1-17.8 (n=3). Little colour variation has been found within this species, although the abdomen may be a bit darker and less distinctly mottled than in the specimens illustrated here. No case of scape break-off was observed in female + +H. cucullus + +sp. nov. + + + +Life history and habitat preferences. + +Mature males of + +H. cucullus + +sp. nov. were found between April and August suggesting reproductive activity mainly in winter (or the dry season in northern latitudes). Mature females were found between March and November, also suggesting that this species is not reproductively active in summer (or the wet season). The species has generally been found in open forests where the spiders build large orb-webs between shrubs and trees. Like + +H. biapicata + +sp. nov. it has been found in a variety of climatic conditions, including semi-arid to arid, tropical and temperate regions. + + + +Distribution. + + +Hortophora cucullus + +sp. nov. has been found throughout all mainland states of Australia, except in the south-eastern states of New South Wales and Victoria. The species has not been found in Tasmania (Fig. +11 +). + + + +Figure 11. +Distribution records of + +Hortophora cucullus + +sp. nov. in Australia. + + + + + \ No newline at end of file diff --git a/data/38/7C/E4/387CE4434E1AFDE8D41EB234DE95CE77.xml b/data/38/7C/E4/387CE4434E1AFDE8D41EB234DE95CE77.xml new file mode 100644 index 00000000000..c16e23e16f7 --- /dev/null +++ b/data/38/7C/E4/387CE4434E1AFDE8D41EB234DE95CE77.xml @@ -0,0 +1,123 @@ + + + +Filling the BINs of life: Report of an amphibian and reptile survey of the Tanintharyi (Tenasserim) Region of Myanmar, with DNA barcode data + + + +Author + +Mulcahy, Daniel G. + + + +Author + +Lee, Justin L. + + + +Author + +Miller, Aryeh H. + + + +Author + +Chand, Mia + + + +Author + +Thura, Myint Kyaw + + + +Author + +Zug, George R. + +text + + +ZooKeys + + +2018 + +757 + + +85 +152 + + + + +http://dx.doi.org/10.3897/zookeys.757.24453 + +journal article +http://dx.doi.org/10.3897/zookeys.757.24453 +1313-2970-757-85 +559E4F4F7C35438089D5BA42A5D38004 + + + + + +Hemidactylus frenatus +Dumeril +& Bibron, 1836 + + + + +Description. +Adult females (n = 2) 52.1-53.2 mm SVL, 51-37 mm TailL; both regenerated; adult male (n = 1) 54.9 mm SVL; 25.3 mm TailL; 23.8 mm HeadL; 43-49% TrunkL/SVL, 13-15% CrusL/SVL, 25-26% HeadL/SVL, 38-39% HeadW/HeadL, 64-66% HeadH/HeadL, 42-44% SnEye/HeadL, 29-33% EyeEar/HeadL. + + +Natural history notes. +A synanthrope. Collected on the outside wall of the hotel in Myeik. + + +General Distribution. +Widespread human commensal, worldwide in subtropics and tropics. + + +Molecular Data. + +Three specimens of +H. frenatus +were collected in Myeik. They were placed in two COIBINs, two (USNM 587030 and 587032) in their own BIN, and USNM 587031 was placed in the same BIN with 18 other +H. frenatus +from Honduras. Our specimens were placed with other specimens in GenBank from the "Myanmar clade" of +H. frenatus +from +Tonione et al. (2011) +. Two other specimens were placed together, on a long branch, sister to all other +H. frenatus +. These specimens were subsequently identified as +H. tenkatei +(see below). + + + +Natural history notes. +Individuals collected from the outside wall of a hotel. + + +Comments. +The House Gecko is a widespread and invasive species. It seldom occurs on vegetation away from human buildings. The tissue gathered from this small sample and barcode analyzed reveals that the Myeik population contains two genetic lineages. + + +Specimens examined. +USNM 587030-032. + + +Red List status. +LC. + + + \ No newline at end of file diff --git a/data/38/7C/E5/387CE56A614EA63042E5FBFF1F43AB09.xml b/data/38/7C/E5/387CE56A614EA63042E5FBFF1F43AB09.xml new file mode 100644 index 00000000000..160e0245c1a --- /dev/null +++ b/data/38/7C/E5/387CE56A614EA63042E5FBFF1F43AB09.xml @@ -0,0 +1,186 @@ + + + +Flora Helvetica - Brassicaceae + + + +Author + +Konrad Lauber + + + +Author + +Gerhart Wagner + + + +Author + +Andreas Gygax + +text + + +2018 +Haupt Verlag + +Bern + + + +Flora Helvetica + + + +480 +566 + + + +book chapter +978-3-258-08047-5 + + + + + +Brassica juncea +(L.) Czern. + + + + + +Artbeschreibung: +Aehnlich +wie + +B. oleracea + +, aber + +Staengel +am Grund borstig behaart. +Grundblaetter +mit grossem Endabschnitt und 1-2 Paaren von Seitenlappen, nicht fleischig, nicht runzelig, schwach behaart. Obere +Blaetter +ungeteilt, stielartig +verschmaelert + +. +Kronblaetter +nur +6-10 mm +lang, kurz benagelt, gelb, +Kelchblaetter +nur +4-6 mm +lang, aufrecht abstehend. Schoten +3-5,5 cm +lang und +2-3 mm +dick, 16-26samig, mit +6-10 mm +langem, samenlosem Schnabel und +8-12 mm +langem, +duennem +Stiel. + + + + +Bluetezeit +: 6-9 + + +Standort und Verbreitung in der Schweiz: +Aecker +, +Schuttplaetze +, gelegentlich eingeschleppt / kollin-montan / + + + +Verbreitung global: Asiatisch + + + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +frisch; Feuchtigkeit +maessig +wechselnd ( ++/- +1-2 Stufen) +Lichtzahl LhellSalzzeichen--
Reaktionszahl Rschwach sauer bis neutral (pH 4.5-7.5)Temperaturzahl Twarm-kollin
+Naehrstoffzahl +N + +naehrstoffreich + +Kontinentalitaetszahl +K +subkontinental (niedrige relative Luftfeuchtigkeit, grosse Temperaturschwankungen, eher kalte Winter)
+
+
+ + +Volksname Deutscher Name: +Sarepta-Senf +, +Ruten-Kohl +Nom +francais +: + +Chou +elance + +, +Moutarde de Sarepta +Nome italiano: +Cavolo giunchiforme + + +
+
\ No newline at end of file diff --git a/data/38/7C/F4/387CF471B6C3BB47525E2ABCB193FEF1.xml b/data/38/7C/F4/387CF471B6C3BB47525E2ABCB193FEF1.xml new file mode 100644 index 00000000000..11cba13ac0c --- /dev/null +++ b/data/38/7C/F4/387CF471B6C3BB47525E2ABCB193FEF1.xml @@ -0,0 +1,73 @@ + + + +Guide to the Vascular Flora of the Savannas and Flatwoods of Shaken Creek Preserve and Vicinity (Pender & Onslow Counties, North Carolina, U. S. A.) + + + +Author + +Thornhill, Robert + + + +Author + +Krings, Alexander + + + +Author + +Lindbo, David + + + +Author + +Stucky, Jon + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1099 +1099 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1099 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1099 +1314-2828-2-1099 + + + + +Cyperus haspan L. + + + +Distribution +Pine savannas. + + +Notes + +Jul-Sep +. Not seen in Shaken Creek Preserve (in perintent habitats) by the senior author. Specimens seen in the vicinity: Sandy Run [ +Haw's +Run]: Taggart SARU 659 (WNC!); Sandy Run [Neck]: Wilbur 53635 (DUKE!). [= RAB, FNA, Weakley] + + + + \ No newline at end of file diff --git a/data/38/7D/87/387D87B3FF81FF80FEAD61C6FACD3370.xml b/data/38/7D/87/387D87B3FF81FF80FEAD61C6FACD3370.xml new file mode 100644 index 00000000000..fda1d31a957 --- /dev/null +++ b/data/38/7D/87/387D87B3FF81FF80FEAD61C6FACD3370.xml @@ -0,0 +1,144 @@ + + + +Ameroculodes miltoni, a new species of estuarine amphipod (Crustacea: Malacostraca: Peracarida: Oedicerotidae) from the southeastern United States + + + +Author + +Foster, John M. + + + +Author + +Heard, Richard W. + +text + + +Zootaxa + + +2002 + +2002-04-12 + + +28 + + +1 +12 + + + +journal article +http://doi.org/10.5281/zenodo.4620161 +1d53d267-f236-45da-b852-56b4cf3525d6 +1175­5326 +4620161 +2EB3FDF9-76B5-44D9-90BD-AEEF4C1E94FC + + + + + + + +A key to the species of + +Ameroculodes + + + + + + + + + + +1 +a Telson quadrate or truncate distally; epimeral plates truncate, quadrate or produced at the posteroventral angle............................................ +2 + + + + +1 +b Telson rounded distally; epimeral plates broadly rounded distally........................................................... + +Ameroculodes miltoni + +, +n. sp. + + + + + + +2 +a Pereopod +3 +, segment +7 +, nail longer than +1 +/ +3 +length of segment +6 +; epimeral plate +2 +produced posteroventrally............. + +Ameroculodes edwardsi +(Holmes, +1905 +) + + + + + +2 +b Pereopod +3 +, segment +7 +, nail shorter than +1 +/ +3 +length of segment +6 +; epimeral plate +2 +quadrate posteroventrally, not produced..................... + +Ameroculodes + +sp. (of + +Bousfield and Chevrier +1996 + +; + +Bousfield, +1973 + +, p. +97 +, plate 19.1) + + + + + + + + \ No newline at end of file diff --git a/data/38/7D/87/387D87B3FF8AFF80FEAD626AFC233157.xml b/data/38/7D/87/387D87B3FF8AFF80FEAD626AFC233157.xml new file mode 100644 index 00000000000..6bd38de8fc9 --- /dev/null +++ b/data/38/7D/87/387D87B3FF8AFF80FEAD626AFC233157.xml @@ -0,0 +1,1355 @@ + + + +Ameroculodes miltoni, a new species of estuarine amphipod (Crustacea: Malacostraca: Peracarida: Oedicerotidae) from the southeastern United States + + + +Author + +Foster, John M. + + + +Author + +Heard, Richard W. + +text + + +Zootaxa + + +2002 + +2002-04-12 + + +28 + + +1 +12 + + + +journal article +http://doi.org/10.5281/zenodo.4620161 +1d53d267-f236-45da-b852-56b4cf3525d6 +1175­5326 +4620161 +2EB3FDF9-76B5-44D9-90BD-AEEF4C1E94FC + + + + + + + +Ameroculodes miltoni + +, +new species +( + +Figs. +1­5 + +) + + + + + + + +Monoculodes edwards +Holmes, +1905 +: +487 + +.– + +Heard +, +1975 + +: 22,25,27; + +Howard, +1975 +: +14 + +; + +Howard et al., +1975 +: +188 + +; + +Sikora et al., +1972 + +: +519,524 +; + +Stickney et al., +1974 +: +519, 525 + +; + +Stickney et al., +1975 +: +519 + +. + + + +Ameroculodes edwardsi +: + +Camp, +1998 +: +130 + + +. + + + +Monoculodes +sp + +. ­­ + +Dorjes & Howard, +1975 +: +152 + +; + +Overstreet & +Heard +, +1982 +: +139 + +. + + + +Monoculodes +sp. A + +: + +Rakocinski et al., +1996 + +; + +Gaston et al., +1996 +: 675 + +, 677, 678. + + + +Monoculodes + +n. sp. +: + +Saloman, +1976 +: +49 + + + + + +Material Examined +.– + +Holotype +: Ovigerous, +female +, 5.0 mm, + +USNM +1001720 + +, +Mississippi Sound adjacent to Biloxi Lighthouse and Lighthouse Pier +, +Biloxi +, +Jackson Co. +, +Mississippi +, depth 1.0 meter, +fie­medium sand substratum +, + + +5 +Jan +1992 + + +, coll. +David Hard + +. + + + + +Paratypes + +: + +Mississippi + +, +Biloxi +, type locality, collection Bba­ +10 +ovigerous +females +, 4.0­6.0 mm + +USNM +1001721 + + +; + +collection BBb­ + +10 +males + +, +4.5 ­ 5.5 mm +, + +USNM + +1001722, + + +25 Jan +1994 + + + + +, coll. +Jan Boyd + +; + +collection Bbc­ +50 +ovigerous +females +and + +10 +males + +, + +USNM +1001723 + +, type locality, coll. +David Hard +, 0 + + +5 +Jan +1992 + + + +; + +collection Bbd­ +45 +ovigerous +females +and + +9 +males + +, + +GCRL +2031 + +, coll. +David Hard + +.– + + +Louisiana + +: collection LPa­ +5 +ovigerous +females +, 5.0 ­ 7.0 mm, + +USNM +1001724 + +, +Lake Pontchartrain +, +Tchefuncta River +, + + +March +1991 + + +, salinity 0.0 ppt, coll. +R.W. Heard + +.– + + +Georgia + +: collection SIa­ ovigerous +female +, +3.5 mm +, + +USNM +1001725 + +, +Sapelo Island +, + + +14 +May +1988 + + +, coll. +R.W. Heard + +.­ + + +Florida + +: collection PBa­ ovigerous +female +, +5.5 mm +, + +USNM +1001726 + +, +Pensacola Bay +, +roadside park at the north base of the bridge causeway +, depth 1.5 meters, +sand substratum, mesohaline conditions +, coll. +R.W. Heard +, + + +25 +Jan +1991 + + + +. + +SBa­ +10 +ovigerous +females +, 5.0 ­ +6.5 mm + +USNM +1001727 + +, SBb­ +male +, 5.0 mm, + +USNM + +1001728, + + +29 Nov +1993 + + + + +, sandy sediments, <1.0 meter, +Sulphur Point at Hathaway Bridge +, +St. Andrew Bay +, coll. +J. M. Foster + +. + + +Other materials examined +: + +[? + +Ameroculodes miltoni + +] +NMCC +acc # +1991 +­ + +1902, + + +26 Feb +1976 + + + +, +Courtney Campbell Causeway +, +Tampa Bay +, +Florida +, +muddy, shelly­sand substratum +, coll. +E. L. Bousfield + +; + + +1 +male + +, + +3 +female + +, +NMCC +acc # +1991 +­ +1905 +, 0 + + +5 +Feb +1976 + + +, +subtidal sand +, Panacea, +Florida +, coll. +E. L. Bousfield + +;. + + +3 +females + +A +. nr. + +miltoni + + +AMNH +16578 + +, +Swan Point +, +New Jersey +, coll. +K. Gosner + +. + + +Comparative materials examined +: + +Holotype +, + +Ameroculodes + +(= + +Monoculodes + +) + +edwardsi (Holmes +1905 +) + +, + +USNM +29243 + +, +male +, +9 mm +, +Woods Hole +, +MA +, coll. + +V. N. +Edwards + + +;– + + +A. edwardsi + +, + +4 +females + +, + +USNM +107800 + +, +York River +, +Virginia +, + + +Feb. +1960 + + + +;.– + + +A. emarginatus +Barnard, +1962 + +, several +females +, + +USNM + +106507, +109352 + + +, and + +108867 +, 10 + +­ +20 +meters, Southern +California +, coll. +J. L. Barnard + +. + + + + +Diagnosis +– Postero­ventral epimeral plates +1­3 +rounded; rostrum blunt, stout, short; uropod +2 +with relatively few dorsal spines; telson rounded posteriorly. + + + + +Description +– adult female.– Head: rostrum blunt, moderately deflexed, slightly recurved, not reaching end of first peduncle article of antenna +1 +, lateral lobe blunt; eyes dorsal, ommatida compact. + + +Antenna one +(setation as illustrated) – longer than peduncle of antenna two; peduncle, article two longer than articles one or three; flagellum shorter than peduncle with eight articles, penultimate and antepenultimate articles bearing aesthetascs. + + + +Antenna +2 + +(setation as illustrated) – peduncle, article +5 +equal to or slightly longer than +4 +; flagellum shorter than peduncle, with +7 +articles. + + +Upper lip +– ovate, slightly expanded distally, apically setose. + + +Lower lip +– outer lobes laterally expanded, recurved posteriorly, medially and apically setose; inner lobe separate, smaller than outer, setose apically. + + + +FIGURE 1 +: + +Ameroculodes miltoni +, + +n sp. +, paratype female BB­a, 4.5 mm (A) whole animal (B) head (C) head, antenna 1­1, female (D) paratype male BB­b, 5.0 mm ­ head, antenna 1­2 male + + + +Mandible +– Left mandible incisor process bearing +4 +jagged teeth ( +1 +depressed, blunt), +4 +serrate spine­setae; lacinia mobilis with +5 +teeth; molar process encircled with overlapping subacute cusps, triturative; palp, article +2 +longest, twice length article +3 +, with double row of long, distally tapered spine­setae, article +3 +with row of +8­10 +short spine­setae on distal half, with +4 +long, simple terminal setae. Right mandible, incisor bicuspidate, bearing broad blade proximally; lacinia mobilis with several small, proximal teeth; +5 +serrate, spine­setae present; molar and palp same as left mandible. + + + +FIGURE 2 +: + +Ameroculodes miltoni + +n. sp. +, paratype female BB­a (A) mandibular palp, article 2­3 (B) left molar and incisor (C) right incisor (D) maxilla 1 (E) maxilliped (F) maxilla 2 (G) lower lip + + + + +Maxilla +1 + +– Inner plate with +2 +simple terminal setae, +1 +finely plumose terminal seta, surface with very fine hair­like setae; outer plate with +9 +terminal spines, +3 +bifurcate distally, +3 +serrate, +3 +blunt; palp with terminal spines and setae. + + + +Maxilla +2 + +– Inner and outer plates equal in length, each with +2 +rows of terminal setae; inner plate with +9 +strong setae, +3 +bifurcate distally. + + +Maxilliped +– Inner plate slightly over half width of outer plate at widest point, with +10 +distal spine­setae; outer plate large, not reaching end of palp article +2 +, inner margin with +11 +spines and several setae; palp article +2 +truncate, widened distally, strong inner marginal, facial, and inner distal setae, article +3 +short, terminal setae, with large, curved terminal claw about half length of article +3 +. + + + +FIGURE 3 +: + +Ameroculodes miltoni + +n. sp. +, paratype female BB­a (A) gnathopod 1 (B) gnathopod 2 (C) pereopod 3 (D) pereopod 4 (E) pereopod 5 + + + + +Gnathopod +1 + +– Article +2 +long, slender, with most marginal and facial setae clustered distally; articles +3 +and +4 +with posterior marginal setae; article +5 +, carpal lobe +44 +% ( +37­ 55 +%) length of article +6 +, barely reaching palmar angle of palm, with +8 +posterior marginal and terminal spines and several simple setae; palm gently convex, with +2 +rows of short and long setae on either side of finely serrate medial ridge, with strong spine at junction with posterior margin of article +6 +; article +7 +(dactyl) fitting palm, with +8 +short, flattened spines on inner margin. + + + +Gnathopod +2 + +– Coxa with +2 +posteromarginal spines and simple ventral setae; article +2 +long, slender, with long, simple posterior and anterior marginal simple setae, articles +3 +and +4 +with posterior setae; article +5 +with long, slender carpal lobe bearing long medial and terminal simple setae, with +1 +short, stout terminal spine, lobe reaching or exceeding palmar angle of article +6 +( +100­115 +%); article +6 +longer and more narrow than article +6 +of gnathopod +1 +, palmar angle with stout spine, palmar margin bearing finely serrate medial ridge bearing rows of short and long simple setae on either; article +7 +as in gnathopod +1 +. + + + +Pereopod +3 + +– Coxa quadrate, with posterior and ventral setae, posterior setae thin, spine­like; oostegite longer and broader than coxal plate; article +2 +, posterior margin with +4 +clusters of long, thin simple setae, anterior margin with a large cluster of setae near anterodistal angle; article +3 +short, with cluster of posterodistal setae; article +4 +90 +% of length of article +5 +, with numerous long, simple setae in rows and clusters on posterior and anterior margin and facially, posterior setae distally tapered; article expanded distally; article +5 +strongly setose posteriorly, with long, distally curved setae, anterior and facial margins with thinner, simple setae; article +6 +over half the length ( +61­75 +%) of article +5 +, anterior margin oblique, with several strong rows of long, distally curved setae, with a dense row of similar setae near posterior margin; article +7 +, short, stout, with +1 +accessory seta, one third length [ +32 +% ( +27­43 +%)] of article +6 +. + + + +Pereopod +4 + +– Coxa broad, widened distally with distal marginal setae and with +1 +long seta at posterodistal angle; article +2 +shorter than coxal plate, with anterior, posterior and facial setae, with clusters of setae at anterodistal angle, distomesial area with several long plumed setae; article +3 +with +2 +anterodistal spines and one plumed setae; article +4 +posterior margin with long, distally tapered setae, outer facial margin with +3 +clusters of long setae, anterior margin without setae except for a large cluster of very long, tapered setae subdistally, length of article +4 +subequal to article +5 +; article +5 +with dense posterior marginal and anterodistal setae, +3 +facial setae; article +6, 75 +% length ( +66­85 +%) of article +5 +, anterior margin with +6 +rows of long, simple setae, posterior and facial margins with fewer, stouter, distally tapered setae; article +7 +, short, stout, approximately one­third length of article +6 +, with +1 +short proximal seta. + + + +Pereopod +5 + +– Coxal plate wider than long, slightly bilobed distally with ventral and posterior marginal setae; gill plate shorter than coxa width; article +2 +subovate, widened medially, tapering distally with two rows of simple, anteromarginal setae, posterior margin with submarginal row of long plumose, outer posterior margin with double row of simple setae; article +3 +short with anterodistal setae; article +4 +, posterior margin with +5 +clusters of thin, simple and plumose marginal setae, posterodistal angle with clusters of longer, distally tapered setae, mesial anterodistal and posterodistal margins with a cluster or long plumed setae; article +5 +, anterior margin with +4 +stout, tapered setae, posterior margin with a posterodistal cluster of simple setae setae; article +6 +longer than article +5 +with +4 +groups of setae on anterior margin, posterior margin with a +5 +clusters of simple setae; article +7 +short, stout, tapered distally, approximately half length of article +6 +. + + + +FIGURE 4 +: + +Ameroculodes miltoni + +n. sp. +, paratype female BB­b (A) pereopod 6 (B) pereopod 7 (C) detail of article 6­7, gnathopod 2 (D) epimera 1­2­3 + + + + +Pereopod +6 + +– Coxal plate about as wide as deep, posterior margin with +4 +spines, distal margin and distal half of anterior margin with short setae; article +2 +subovate, anterior margin, proximal half with simple setae, distal half with long plumed setae, outer surface with submarginal row of simple setae, posterior margin with short simple setae, with medial submarginal row of long plumose setae; article +3 +, short, with anterodistal setae; article +4 +posterior margin with simple setae increasing in length distally, with plumed setae distally, anterodistal angle with plumed and simple setae, anterior margin with simple setae; article +5 +shorter than article +6 +, with long, curved setae on posterodistal margin, anterior margin with simple setae; article +6 +with long, tapered setae on posterior margin, sparse on anterior margin; article +7 +short, stout, tapered distally, approximately half length of article +6 +. + + + +Pereopod +7 + +– Coxa short and wide with short posterior spines; article +2 +, expanded posteriorly, posterior margin with short, thin spines, mesial surface with row of long plumose setae, anterior margins with +4­5 +short spines; anterodistal angle with a cluster of +4­5 +spines; article +3 +with +5 +strong anterodistal spines; article +4 +, anterodistal angle with +4 +spines, posterior margin with +3 +clusters of spines, article +5 +subequal to article +4 in +length, with +2 +groups of +2 +spines on posterior margin and +3 +groups of +2­4 +spines on anterior margin, anterodistal and posterodistal angles with spine clusters; article +6 +subequal to article +5 in +length with +4 +clusters of +2­3 +anterior marginal spines, distal margin ringed with spines; article +7 +subequal to article +6 in +length, anterior margin with +4 +spine groups, distal margin with +2­4 +long, plumose setae (often lost in preserved specimens). + + +Oostegites +– Present on gnathopod +2 +through pereopod +5 +, densely setose marginally. + + +Epimeral plates +– Epimeron +1 +with gently curved ventral margins and corners, without setae; epimeron +2 +ventral margin almost convex, broadly rounded posteriorly and anteriorly with submarginal setae; epimeron +3 +, ventral margin straight, with marginal and submarginal setae, corners abruptly rounded. + + +Pleopods +– Pleopods +1­3 +of equal length, peduncle shorter than rami, with finely plumose marginal setae, simple facial setae, +2 +retinacula (coupling hooks) distally on each peduncle, rami with +13­15 +setose articles. + + + +Uropod +1 + +– Peduncle longer than rami, two proximoventral spines near articulation with urosome, one dorsodistal spine at the base of each ramus; outer margin with a row of +6­9 +short spines, inner margin with +2­4 +thin marginal spine­setae; inner ramus longer than outer, both with +2­4 +marginal spine setae, inner margins of both rami minutely serrate, terminal spines absent. + + + +FIGURE 5 +: + + +Americulodes +miltoni + + +n. sp. +, paratype female BB­b (A) uropods 1­2­3, lateral view (B) telson + + + + +Uropod +2 + +– Peduncle subequal to outer ramus in length, with +1­2 +inner marginal spines, +4­5 +outer marginal spines, outer distal margin with a short stout spine; inner ramus longer than outer, both rami with +2­4 +marginal spines on both outer margins, inner margins of both rami minutely serrate, terminal spines absent. + + + +Uropod +3 + +– Peduncle about half length of inner ramus, with several distal spines, inner ramus longer than outer with +2 +marginal spines; outer ramus with +1 +spine, terminal ramal spines absent. + + +Telson +– Tapering to gently rounded distal margin with +2 +posterodorsal marginal setae. + + +Adult male +– Similar to female in most aspects, but distinctly smaller. Antenna +2 +much longer than antenna +1 +, with +11­13 +articles bearing aesthetascs. Length of pereopod +7 in +relation to body length much longer in male than in female. + + + + +Etymology +– This species is named in honor of the late Milton Foster, naturalist and father of the senior author. + + + + +FIGURE 6 +: + + +Ameroculodes edwardsi + +(Holmes, 1905) + +holotype, 9 mm, USNM 29243 (A) gnathopod 2 (B) gnathopod 1 (C) head, lateral (D) pereopod 3 (E) pereopod 6 + + + + +Remarks +– In southeastern waters, + +Ameroculodes miltoni + +has been confused with its distinctly larger relatives, + +Ameroculodes edwardsi + +and + +Deflexilodes intermedius + +, both reliably known only from the cold temperate waters of northeastern North +America +(north of New +Jersey +). Besides its much smaller size, + +A. miltoni + +differs from + +A. edwardsi + +(see + +Fig. +6 + +) by having the ( +1 +) epimeral plates +1­3 +rounded (quadrate in + +A. edwardsi + +), ( +2 +) rostrum blunt, stout, and short (more flattened and longer in + +A. edwardsi + +), ( +3 +) uropod +2 +peduncle with larger and fewer dorsal spines (numerous smaller spines in + +A. edwardsi + +), and ( +4 +) telson subovate and rounded posteriorly (truncate in + +A. edwardsi + +), ( +5 +) basis of pereopod +7 +relatively narrow (broad in + +A. edwardsi + +). + + + +Deflexilodes intermedius + +, like + +A. miltoni + +, has rounded epimeral plates; it is, however, readily distinguished by the dactyls of the +3 +rd and +4 +th pereopods, which are well­developed and elongate (those of + +A. miltoni + +are reduced and short). + + +In the northern Gulf of +Mexico +, + +Ameroculodes miltoni + +occasionally co­occurs with + +Hartmanodes + +(= + +Monoculodes + +) + +nyei +(Shoemaker, +1933 +) + +. The two species are immediately distinguishable by the distinctly longer carpal lobes of gnathopods +1 +and +2 +and the longer more “hooked” rostrum of + +H. nyei + +, as well as by setation of the uropods and the shape of the telson. The only other shallow water oedicerotid known from the waters of the southeastern +United States +, which occasionally co­occurs with + +A. miltoni +, + +is + +Americhelidium + +(= + +Synchelidium +) americanum + +( + +Bousfield, +1973 + +). However, this species is characterized by having a chelate second gnathopod. Actually, + +A. miltoni + +may have its closest affinities to the eastern Pacific species + +A. hartmani + +and + +A. emarginatus + +. + + + +Ecological observations – +Ameroculodes miltoni + +is normally associated with estuarine and coastal bay habitats in a wide range of salinities (< +1 +°/ to +35 +°/), occurring on medium to fine sand or sand­silt substrata. It appears to be an important bionomic component of estuaries of the northern Gulf of +Mexico +. At its +type +locality, a shallow sand bottom adjacent to the Biloxi Lighthouse Pier, + +A. miltoni + +is an important component in the diet of juvenile spot, + +Leiostomus xanthurus +Lacèpéde + +during March, April, and May (R. +Heard +, per. obs.). Under the name “ + +Monoculodes edwardsi + +” it also has been reported in the diets of other estuarine fishes ( + +Sikora et al. +1972 + +, + +Stickney et al. + +1974, +1975 + + +, + +Heard +1975 + +). + +Ameroculodes miltoni + +is an excellent swimmer and enters the water column at night. In +Georgia +and Mississippi estuaries, it can represent an important part of the hypoplankton in night plankton tows (R. +Heard +, pers. obs.). + + + + \ No newline at end of file diff --git a/data/38/7D/87/387D87B3FF8AFF8BFEAD6727FD28320A.xml b/data/38/7D/87/387D87B3FF8AFF8BFEAD6727FD28320A.xml new file mode 100644 index 00000000000..e62ac6fd59a --- /dev/null +++ b/data/38/7D/87/387D87B3FF8AFF8BFEAD6727FD28320A.xml @@ -0,0 +1,128 @@ + + + +Ameroculodes miltoni, a new species of estuarine amphipod (Crustacea: Malacostraca: Peracarida: Oedicerotidae) from the southeastern United States + + + +Author + +Foster, John M. + + + +Author + +Heard, Richard W. + +text + + +Zootaxa + + +2002 + +2002-04-12 + + +28 + + +1 +12 + + + +journal article +http://doi.org/10.5281/zenodo.4620161 +1d53d267-f236-45da-b852-56b4cf3525d6 +1175­5326 +4620161 +2EB3FDF9-76B5-44D9-90BD-AEEF4C1E94FC + + + + + + +FAMILY +OEDICEROTIDAE +Liljeborg, +1865 + + + + + + + +Ameroculodes + +Bousfield and Chevrier, +1996 + + +, emended diagnosis + + + + +Diagnosis +. – Maxilliped, outer plate bearing spine setae only; palp with article +2 +broad, distally truncate. Gnathopod +1 +, carpal lobe of medium length and width, reaching palmar angle. Pereopods +2­3 +, carpus longer than propodus; propodus broad, subovate, narrowing distally; dactyl short, one third or less length of propodus. Pereopods +4­5 +, merus relatively short, strongly expanded distally; dactyl short, one half or less length of propodus. Pereopod +7 +, carpus slightly longer than merus, subequal to propodus in length; dactyl, posterior margin strongly setose, bearing long natatory setae. Uropods +1­3 +, tips of rami not extending subequally, those of uropod +3 +shorter than those of uropod +1­2 +. Telson subquadrate or rounded apically. + + + + +Remarks +.– Because the new euryhaline species here described from southeastern +U. S. +estuaries appears to have its closest affinities with + +Ameroculodes + +, we here emend this genus to receive it. As species within the genus + +Monoculodes +sensu + +Bousfield and Chevrier ( +1996 +) + + +also have rounded or subquadrate epimeral plates, we consider this a specific, rather than a generic, character within the genus + +Ameroculodes + +, as well. The short dactyls of pereopods +3­6 +, especially those of pereopods +3 +and +4 +, appear to be the best diagnostic character for the genus + +Ameroculodes + +. + + + + \ No newline at end of file diff --git a/data/38/7E/34/387E34C5C9FF19AE5CE2B237EFEF9050.xml b/data/38/7E/34/387E34C5C9FF19AE5CE2B237EFEF9050.xml new file mode 100644 index 00000000000..87e7a1fda8e --- /dev/null +++ b/data/38/7E/34/387E34C5C9FF19AE5CE2B237EFEF9050.xml @@ -0,0 +1,356 @@ + + + +The Crematogaster (Hymenoptera, Formicidae, Myrmicinae) of Costa Rica. + + + +Author + +Longino, J. T. + +text + + +Zootaxa + + +2003 + +151 + + +1 +150 + + + + +http://antbase.org/ants/publications/20256/20256.pdf + +journal article +20256 +9813210B-5B9F-4FDE-86DD-3AE55166EC9C + + + + +Crematogaster carinata Mayr +1862 + + + +Plate 1 + + + +Crematogaster carinata Mayr +, 1862:768. + +Syntype +workers: +Brazil +, +Rio de Janeiro +( +Novara +) [ +NMW +, +MCSN +] (examined, +NMW +worker here designated +LECTOTYPE +) + +. Emery, 1922:136: combination in +C. (Orthocrema) +. + + +Crematogaster +(species not indicated): Forel 1898:380 (description of parabiosis). + + +Crematogaster limata r. parabiotica Forel +, 1904b:683. + +Syntype +worker: +Colombia +, +Magdalena +, +Orihueca +, parabiotic with +Dolichoderus debilis +(coll. +Forel +) [ +MHNG +] (examined, worker here designated +LECTOTYPE +) + +. Forel, 1912:217: description of queen. Emery, 1922:136: combination in +C. (Orthocrema) +. Wheeler, W.M. 1921b:152; Wheeler, W.M. 1923:3; Kutter, 1931:61; Santschi, 1939:161; Kempf, 1972:88: subspecies of +limata +. +NEW SYNONYMY + + +Crematogaster parabiotica Forel +(part): Wheeler, W.M. 1921a. + + +Crematogaster cf. limata parabiotica Forel +(part): Davidson 1988, Seidel et al. 1990, Davidson et al. 1990. + + + +Range +Costa Rica to Brazil (Rio de Janeiro), Bolivia. + + +Description of worker +Color red brown; mandibles, antennal club, and tarsi usually lighter yellow; workers monomorphic in size. +Mandibles smooth and shining; clypeus usually with 5-6 longitudinal carinulae, these may be more abundant, making clypeus uniformly striate, or they may be nearly absent, making clypeus smooth and shining, especially medially; head about as long as wide, subquadrate, with emarginate posterior border; antenna with distinct two-segmented club, or third segment from end somewhat enlarged, blurring distinction between two and threesegmented club; scapes with abundant long erect setae; when scapes laid back from antennal insertions, they slightly surpass margin of vertex; face largely smooth and shining, with variable extent of striated region between antennal insertion and eye, and whorled above antennal insertion; face covered with abundant long flexuous white setae, no appressed pubescence; in face view abundant setae project from lateral and posterior margins. +Promesonotum in profile forming evenly convex surface, varying from flattish to forming peak at juncture of pro and mesonotum; propodeal suture deep in dorsal view but obscured in profile due to lateral carinulae that bridge the suture; posterior mesonotum curves smoothly into horizontal dorsal face of propodeum; propodeal spines short, projecting posteriorly such that they are more or less in same plane as dorsal face of propodeum; dorsal and posterior face of propodeum appear well differentiated in lateral view, the dorsal face confluent with the horizontal spines, the posterior face sloping down to petiolar insertion, but faces less differentiated medially; pronotal dorsum with variably developed longitudinal carinulae, strongest laterally, becoming weaker medially, interspaces smooth and shining; mesonotal dorsum with two strong, subparallel lateral carinae, interspace smooth and shining or with faint longitudinal carinulae; dorsal face of propodeum striatorugose, rugulae extending onto spines, posterior face smooth and shining; side of pronotum smooth and shining; katepisternum and ventral portion of side of propodeum variously punctatorugose; dorsal portion of side of propodeum smooth and shining; mesosomal dorsum with abundant long flexuous white setae, setae on pronotal humeri longest; femora and tibiae with abundant long erect setae. +Petiole in side view subtrapezoidal, varying in length and degree of narrowing anteriorly, weakly punctate to nearly smooth; anteroventral tooth well developed, often forming a right-angle to short acute tooth; dorsal face of petiole smooth and shining, elongate, widest posteriorly, regularly tapering anteriorly, with a long flexuous seta on each posterolateral tubercle and varying number of short setae along posterior border; postpetiole lacking ventral tooth, globular in dorsal view, with abundant erect setae; fourth abdominal tergite smooth and shining, with abundant long flexuous erect white setae, no appressed pubescence. +Measurements +HL 0.561, 0.528, 0.657; HW 0.604, 0.563, 0.722; HC 0.565, 0.507, 0.664; SL 0.485, 0.512, 0.612; EL 0.130, 0.139, 0.175; A11L 0.215; A11W 0.101; A10L 0.113; A10W 0.089; A09L 0.068; A09W 0.064; A08L 0.051; A08W 0.051; WL 0.615, 0.585, 0.744; SPL 0.077, 0.109, 0.148; PTH 0.148, 0.137, 0.166; PTL 0.207, 0.213, 0.250; PTW 0.144, 0.138, 0.174; PPL 0.169, 0.129, 0.178; PPW 0.162, 0.119, 0.166; CI 108, 107, 110; OI 23, 26, 27; SI 86, 97, 93; PTHI 71, 64, 66; PTWI 70, 65, 70; PPI 96, 92, 93; SPI 13, 19, 20; ACI 0.64. +Queen +A normal queen (dorsal face of propodeum drops steeply from postscutellum and much of propodeum appears ventral to scutellum and postscutellum, Fig. 1) with general shape, sculpture, and pilosity characters of the worker; size characters as in Figures 4 and 5. + + +Biology + +Crematogaster carinata +is a biologically complex species and there is almost certainly some degree of genetic structuring that is not readily revealed by external morphology. This species and its close relative +C. levior +often have large polygynous colonies that blanket large sections of forest, with various degrees of mutual foraging and nesting with other unrelated ant species. Forel observed this species nesting with +Dolichoderus debilis +in Colombia, and coined the term parabiosis for the mutual sharing of nest space and foraging columns by multiple species (Forel 1898). Further examples of parabiosis involving +carinata +(as +parabiotica +) were described by Wheeler (1921a). + + +In the Atlantic lowland forests of northeastern Costa Rica, including coastal strand vegetation, +C. carinata +forms large polygynous, perhaps even unicolonial colonies. Columns of workers are spread over second growth vegetation and multiple crowns of trees, with small clusters of physogastric queens, brood, and workers dispersed in dead twigs and branches and under epiphytes. There is no obvious colony center, and it is difficult to discern colony boundaries. At La Selva Biological Station it is one of the most common species in the canopy. It occurred in 24 of 52 canopy fogging events. In an old treefall I once found a small aroid with a +carinata +nest in and around the root ball. The ants had covered the roots with a mass of carton material to form a nest volume about the size of a large orange. Inside were abundant workers, brood, and 43 dealate queens. Some of these queens had torn remnants of wings, suggesting they never left the nest for a nuptial flight and perhaps never mated. In general when multiple queens are found in nests they are evenly distributed in the nest volume, individually or in pairs. Brood is segregated by size. I observed a similar occurrence of large polygynous colonies in the Santa Marta region of Colombia, the same site as Forel's original observations of parabiosis. In contrast to these observations of polygyny, discrete nests with single physogastric queens seem to be the rule in the Pacific and southeastern Atlantic lowlands of Costa Rica, and at some sites in Venezuela. + +On occasion I find aggregations of workers only, with no brood. All the dead sticks in a patch of forest understory will be filled with workers. The nest aggregation will be bounded, with all nests within about a meter of each other, but no colony center or area with brood can be found. + +In different parts of its range, in both polygynous and monogynous forms, +Crematogaster carinata +may form parabiotic associations with other ants. In the La Selva forest canopy it cohabits large ant gardens with +Odontomachus panamensis +. Because the ant gardens are conspicuous and packed with +Crematogaster +workers and brood, it can appear that the +Crematogaster +are a specialized associate with +Odontomachus +, but closer inspection reveals that the ant gardens are nodes of higher +Crematogaster +density in a sea of thinly spread +Crematogaster +nests. It is possible that the ants in +Odontomachus +nests are genetically and behaviorally differentiated from those in the diffuse polydomous colonies, but I have not found any evidence for this based on external morphology. + + +In the Pacific lowlands of Costa Rica I have twice seen parabiotic associations between +carinata +and +Dolichoderus +species. At Carara I observed a parabiotic association between +carinata +and +D. debilis +. Several nests were in a cluster of dead branches. +Crematogaster +workers and brood were distributed in multiple chambers, and one chamber contained a single physogastric queen. The nests of the two species were contiguous and interdigitated, with interconnections among chambers, but they were still largely segregated. In general the +Crematogaster +occupied smaller and more peripheral chambers, while the +Dolichoderus +occupied larger chambers in the center of the branches. In some peripheral chambers I found workers of both species together, but these chambers never contained brood. Any chamber with brood always contained only one species. In Corcovado National Park I observed parabiotic foraging involving +carinata +and +D. inermis Mackay +. Workers of both species were using the same foraging trails, and both species occurred together in clusters of non-foraging workers. Davidson has multiple observations of parabiotic foraging between +carinata +and +D. debilis +in Peru (pers. comm.), and many similar observations are reported by Forel (1898) and Wheeler (1921a). + + +Wherever I have observed +carinata +it makes use of carton construction to a variable extent. Construction may be as small as a 2cm diameter shelter over a single scale insect. Several times I have seen a 5-10cm wide globular mass of carton extending from the end of a rotten stick or investing epiphyte roots, extending the nest volume. In very humid areas these small carton nests may sprout epiphyte seedlings and in some cases form small ant gardens. Workers form large and more fully developed ant gardens only when in the presence of a larger parabiotic associate. + +Workers may be found foraging day or night, and they are generalized omnivores. I have seen them scavenging dead or wounded insects, they recruit to carbohydrate and protein baits, and they are frequent visitors at extrafloral nectaries. + + +Comments + +Costa Rican species in the +limata +complex are +brasiliensis +, +carinata +, +limata +, and +tenuicula +. All have abundant erect flexuous setae on the face, moderate length to short posteriorly directed propodeal spines, and elongate tapering petioles. The four species can be difficult to separate. They differ primarily in the nature of the ventral processes of the petiole and postpetiole. +Crematogaster carinata +has a squared-off anteroventral petiolar process and no postpetiolar process. Both +brasiliensis +and +tenuicula +have ventral postpetiolar processes. +Crematogaster limata +usually lacks a petiolar process but can be very like +carinata +in some cases. +Crematogaster limata +is a larger ant with longer propodeal spines. +Crematogaster carinata +may also be confused with +foliocrypta +, but +foliocrypta +has appressed rather than erect tibial pilosity. + + +Crematogaster carinata +is also very similar to the South American species +Crematogaster levior Longino +(see Miscellanea). The two species are not cleanly separable on morphological grounds. In this revision I have restricted +C. levior +to a specialized parabiotic associate of +Camponotus femoratus (Fabricius) +. +Crematogaster levior +and +Camponotus femoratus +inhabit ant gardens throughout Amazonian South America. All +Crematogaster +material collected from these ant gardens has the worker pronotum completely smooth and shining. In contrast, I have identified as +carinata +all material with longitudinal carinulae on the pronotum. However, on purely morphological grounds there is continuous variation from strongly carinate forms, to forms with faint traces of carinulae, to the completely smooth pronotum of +levior +. +Crematogaster levior +is polygynous and polydomous like some populations of +carinata +. +Crematogaster levior +is always parabiotic with +Camponotus femoratus +, while +C. carinata +is facultatively parabiotic with other large ants in the genera +Dolichoderus +and +Odontomachus +. + + +Further evidence for separate species has been found by D. Davidson at her study site at Cocha Cashu Biological Station in Amazonian Peru. In early studies of ant gardens and their ants (Davidson 1988, Seidel et al. 1990, Davidson et al. 1990) I helped identify the +Crematogaster +and I failed to differentiate +levior +and +carinata +. More recent observations on behavior and defensive chemistry suggest discrete sympatric forms, with +levior +inhabiting ant gardens with +Camponotus +and +carinata +found outside those gardens (Davidson pers. comm.). Davidson has discovered that +levior +has lost its chemical defense and instead relies on the defensive capabilities of +C. femoratus +. In contrast, +carinata +has retained chemical defenses. Reflecting the differences in defensive chemistry, +levior +does not elevate the gaster when disturbed; +carinata +does. +Crematogaster carinata +is often found living parabiotically with +Dolichoderus debilis +, and in this case it is the +Dolichoderus +that has lost its chemical defense, relying on the +Crematogaster +. Davidson's observations on +carinata +in Peru not withstanding, one should not assume that +carinata +exhibits the same behavior and defensive chemistry throughout the range. It would be worth investigating whether +carinata +at La Selva Biological Station, which lives in ant gardens with the aggressive species +Odontomachus panamensis +, exhibits behavior and chemistry more like +levior +. In contrast, the +carinata +from Costa Rica's Pacific slope, which is monogynous and parabiotic with non-aggressive +Dolichoderus +, might be like Peruvian +carinata +. + + +Forel's brief description of +parabiotica +was followed by a list of specimens: Colombia, Magdalena, Orihueca, parabiotic with +Dolichoderus debilis (Forel) +; Para ( +Goeldi +); Costa Rica (Pittier); and Brazil, Amazonas, Jurua, Jurua Miry, among leaf bases of +Tillandsia +No. 5734 (Ule). I examined the Colombian and Ule's Brazilian material under +parabiotica +at MHNG. The Colombian material had carinate pronota and matched my collections from the Santa Marta area. Ule's Brazilian material, probably from ant gardens, had smooth pronota. Forel's published description of +parabiotica +suggested that the Ule specimens might be a separate variety. Among the specimens at MHNG a worker from Orihueca has "typus" written on the label. Other labels have "cotypus" or no indication of type status. It appears that Forel based the description primarily on the Colombian material and I am forced to treat the Orihueca specimen as the lectotype of +parabiotica +and synonymize it under Mayr's +carinata +. The Ule specimens I identify as +levior +. Following this hypothesis of species boundaries, Wheeler's (1921a) discussion of parabiosis included observations of +carinata +living parabiotically with +Dolichoderus +, and +levior +living parabiotically with +Camponotus femoratus +. + + +Within +carinata +, there is pronounced variation in the degree of anterior narrowing of the petiole in side view, strength of pronotal carinulae, size of propodeal spines, and some details of queen size and petiole shape. +Crematogaster levior +is more likely to be a "good" species, in terms of phylogeny and/or genetic similarity. +Crematogaster carinata +, with its greater geographic range and morphological variability, is more likely to be a set of allopatric or parapatric species, or even a set of broadly sympatric cryptic species. + + + + \ No newline at end of file diff --git a/data/38/7E/50/387E50633471E9FA43990E17E6328EA8.xml b/data/38/7E/50/387E50633471E9FA43990E17E6328EA8.xml new file mode 100644 index 00000000000..052aa31eabd --- /dev/null +++ b/data/38/7E/50/387E50633471E9FA43990E17E6328EA8.xml @@ -0,0 +1,201 @@ + + + +Australian gall-inducing scale insects on Eucalyptus: revision of Opisthoscelis Schrader (Coccoidea, Eriococcidae) and descriptions of a new genus and nine new species + + + +Author + +Hardy, Nate B. + + + +Author + +Gullan, Penny J. + +text + + +ZooKeys + + +2010 + +58 + + +1 +74 + + + + +http://dx.doi.org/10.3897/zookeys.58.507 + +journal article +http://dx.doi.org/10.3897/zookeys.58.507 +1313-2970-58-1 + + + + +Tanyscelis conica (Fuller) +comb. n. +Figs 2a,b11 + + + + +Opisthoscelis conica +Fuller 1897: 1346 +; +Fuller 1899: 464 +. + + + +General. + +Fuller's +(1897: 1346) original description of +Opisthoscelis conica +is very brief: "Upon one side of the leaf arises the conical apex, whilst on the other the gall protrudes as +a +hemisphere." Later +Fuller (1899) +published a more detailed description with an illustration of three galls of females on a leaf and a hind leg of an adult female (plate XV, figs 33-34). The galls in +Fuller's +drawing are very similar to syntype galls housed in the SAMA (see "Material examined" for details), but no insects have been found in the SAMA or elsewhere (e.g., not in the South African National Collection of Insects where some other Fuller material is housed). The type locality of +Opisthoscelis conica +was given as Midland Junction in +Fuller (1897) +but as Swan River in +Fuller (1899) +, however it is unlikely that there were two localities for this species because Fuller published the second paper from South Africa based on notes that he had made during eight or nine months spent collecting in Perth prior to his 1897 paper. Midland Junction, now the suburb of Midland, is several km east of the Swan River and, in the 1890s, it was a railway station and associated village. + + + +Gall +(Fig. 2a,b). Female. On leaf. Height 5.0-7.0 mm (= total height above and below leaf blade), width 5.0-9.5 mm. Gall opening slit-like, 0.5-0.8 mm long; on abaxial or adaxial surface, but all galls opening on same surface on any one leaf. Side of gall with opening conical, other side convex, globose (Fig. 2b). +Male. Not known. + + +Adult female + +(Fig. 11) (n = 8). Body outline turbinate, margin incised at intersegmental boundaries, length 2.5-3.7 mm, greatest width 1.1-2.5 mm; abdomen tapered, about as long as head + thorax, extending far beyond femur. Eyespots small, each 18-25 mm wide. Antennae 1-segmented, each 35-108 mm long. Frontal lobes difficult to see, each ca 170 +µm +long, 200 +µm +wide. Tentorial box 350-470 mm long. Pump chamber 30-43 +µm +long, 38-48 +µm +wide. Labium 85-113 mm long, 95-140 mm wide. Spiracles 70-105 mm long, 45-63 mm wide across atrium. Fore and mid legs small sclerotic protuberances; fore leg 20-35 +µm +long, with 6-8 setae; mid leg larger, 38-80 +µm +long, with 10-12 setae. Hind legs robust and elongate; coxa 180-260 +µm +long, trochanter about as a long as femur, the two combined 450-610 +µm +long, tibia and tarsus fused, forming straight, sword-like segment 720-1880 +µm +long; claw and digitules absent; translucent pores dense throughout distal region of dorsal and ventral surfaces of tibiotarsus; femur-tibia articulation poorly developed. Anal opening poorly formed, 15-28 +µm +wide, surrounded by dense cluster of setae. + + +Dorsum. Derm membranous. Dorsal setae robust, often slightly curved, 15-138 mm long; dense over head and thorax, forming transverse band of longer setae on each abdominal segment. Macrotubular ducts 10-15 mm long, dermal orifice with a rim 5 mm wide; in transverse row on each of abdominal segments +III-VI +. Microtubular ducts absent. Quinquelocular pores 6-8 +µm +in diameter, scattered over dorsum. + +Venter. Derm on abdomen with bands of microtrichia. Setae 15-150 mm long, in a transverse row across each abdominal segment, dense along margin and submargin of head and thorax, medial cluster on mesothorax and metathorax. Macrotubular ducts similar to those on dorsum, in sparse transverse rows across each of abdominal segments III-VI. Microtubular ducts absent. Quinquelocular pores similar to those on dorsum, similar in distribution to ventral setae. + + +Material examined. + +Type material: AUSTRALIA: Western Australia: 3 syntype galls of females, dry and empty (2 dissected open, third gall parasitised), on 2 leaves, all on pin-mount, 2 labels: " +Opisthoscelis +Schrader / conica, Fuller, sp. n. Type / Perth, W. Australia / C. Fuller / 28.7.97" and " Perth, W. A. / +Opisthoscelis +/ conica Fuller / m/s / 28.7.97" (SAMA). + + +Additional material: + +AUSTRALIA: South Australia: 4 first-instar nymphs: ex galls on leaves, +Eucalyptus dumosa +, Danggali Conservation Park, Main Road site 1, -33.29°; 140.59°, 21 Apr., 1996, PJG (ANIC); 2 adult females, 35 first-instar nymphs: ex leaf galls, +Eucalyptus dumosa +, Danggali Conservation Park, Main Road, Site 1, -33.29°; 140.59°, 22 Apr., 1996, PJG (ANIC); 2 adult females: ex leaf galls, +Eucalyptus dumosa +, Danggali Conservation Park, Main Road, Site 4, -33.28°; 140.59°, 23 Apr., 1996, PJG (ANIC); 2 adult females: ex leaf galls, +Eucalyptus dumosa +, Danggali Conservation Park, Tipperary +Dam- +Canopus Road, Site 6, -33.27°; 140.72°, 24 Apr., 1996, PJG (ANIC). Victoria: 2 adult females: ex leaf galls, +Eucalyptus +sp.(mallee), 25 km N of Ouyen, on Calder Hwy, 22 Apr., 1994, T. Murphy (ANIC); 2 adult females: +Eucalyptus incrassata +, Big Desert, Moonlight Tank, 13 Feb., 1977, PJG (ANIC); 1 adult female: ex leaf gall +Eucalyptus incrassata +, Big Desert, Wyperfeld National Park, 13-18 Aug., 1977, T. P. +O'Brien +(ANIC); 2 adult females: ex leaf galls, +Eucalyptus dumosa +, ca 20 km N of Hattah, Calder Highway, -34.68°; 142.25°, 5 Feb., 2005, PJG and NBH, NH48 (ANIC); 1 adult female: ex leaf gall, +Eucalyptus dumosa +, ca 20 km W of Mittyack, Calder Highway, -35.17°; 142.45°, 5 Feb., 2005, PJG and NBH, NH76 (ANIC). Western Australia: 6 adult females: ex leaf galls, +Eucalyptus?wandoo +, 2.3 km S of Boddington and 18 km SSW of North Bannister, 5 Jan., 1986, PJG (ANIC); 2 adult females: ex leaf galls, +Eucalyptus wandoo +, 44 km N of Williams, Albany Hwy, 29 Mar, 1978, PJG (ANIC); 3 adult females, 1 second-instar female: ex leaf galls, +Eucalyptus accedens +, Coomallo, off Brand Hwy, on dam edge, -30.23°; 115.40°, 3 Dec., 1990, PJG (ANIC); 1 adult female, 3 second-instar females: ex galls on leaves, +Eucalyptus wandoo +, Woodanilling, Great Southern Hwy, at crossroads, -33.57°; 117.43°, 1 Dec., 1994, PJG (ANIC). + + + + +Comments. + +The adult female of +Tanyscelis conica +would be difficult to confuse with the adult female of any other known species of +Tanyscelis +. The fusion of the hind tibia and tarsus into a broad, sword-like appendage is unique. Both the form of the dorsal setae (robust and slightly curved) and their dense distribution also separate adult females of +Tanyscelis conica +from those of other species. Known populations of +Tanyscelis conica +occur in two disjunct clusters, one centered around Perth in southwest Western Australia, and the other in forest reserves in northwestern Victoria and southeastern Australia (e.g., Danggali Conservation Park, Wyperfield National Park, Hattah-Kulkyne National Park). Despite the great distance separating the two, ca 2000 km, the morphology is homogeneous. +Tanyscelis conica +is the only species of +Tanyscelis +known from Western Australia. Only one species of +Opisthoscelis +, the type species +Opisthoscelis subrotunda +, has been collected from Western Australia, in the Kimberley region, which is a great distance (> 1,500 km) north of Perth. +Tanyscelis conica +is also the only known species of +Tanyscelis +or +Opisthoscelis +known to feed on mallee eucalypt species in the section +Dumaria +, and +along +with +Opisthoscelis ungulifinis +, is one of only two species in this group known to feed on eucalypts in the section +Bisectae +. + + + + \ No newline at end of file diff --git a/data/38/7E/6F/387E6F11676E5101B53BA7246A3EF440.xml b/data/38/7E/6F/387E6F11676E5101B53BA7246A3EF440.xml new file mode 100644 index 00000000000..094ef92b5ee --- /dev/null +++ b/data/38/7E/6F/387E6F11676E5101B53BA7246A3EF440.xml @@ -0,0 +1,85 @@ + + + +Distribution patterns of Chinese Cixiidae (Hemiptera, Fulgoroidea), highlight their high endemic diversity + + + +Author + +Luo, Yang +Key Laboratory of Plant Protection Resources and Pest Management, Ministry of Education, Entomological Museum, College of Plant Protection, Northwest A & F University, Yangling, Shaanxi 712100, China, Yangling, China + + + +Author + +Bourgoin, Thierry +https://orcid.org/0000-0001-9277-2478 +Institut de Systematique, Evolution, Biodiversite, ISYEB-UMR 7205, MNHN-CNRS-Sorbonne Universite-EPHE-Univ. Antilles, Museum national d'Histoire naturelle, CP 50, 57 rue Cuvier, F- 75005, Paris, France +thierry.bourgoin@mnhn.fr + + + +Author + +Zhang, Jia-Lin +Key Laboratory of Plant Protection Resources and Pest Management, Ministry of Education, Entomological Museum, College of Plant Protection, Northwest A & F University, Yangling, Shaanxi 712100, China, Yangling, China + + + +Author + +Feng, Ji-Nian +Key Laboratory of Plant Protection Resources and Pest Management, Ministry of Education, Entomological Museum, College of Plant Protection, Northwest A & F University, Yangling, Shaanxi 712100, China, Yangling, China +jinianf@nwsuaf.edu.cn + +text + + +Biodiversity Data Journal + + +2022 + +2022-01-24 + + +10 + + +75303 +75303 + + + + +http://dx.doi.org/10.3897/BDJ.10.e75303 + +journal article +http://dx.doi.org/10.3897/BDJ.10.e75303 +1314-2828-10-e75303 +07802C19F192544C9F561556F25CA5C4 + + + + +Betacixius euterpe Fennah, 1956 + + + + +Betaxixius euterpe +Fennah, 1956: 458; Zhang & Chen, 2011b: 50. + + + +Distribution + +China: Guangdong ( +Fennah 1956 +). + + + + \ No newline at end of file diff --git a/data/38/7F/03/387F03330F06E0FEADEA338C2EB2B314.xml b/data/38/7F/03/387F03330F06E0FEADEA338C2EB2B314.xml new file mode 100644 index 00000000000..df66a8a1bad --- /dev/null +++ b/data/38/7F/03/387F03330F06E0FEADEA338C2EB2B314.xml @@ -0,0 +1,46 @@ + + + +Catalogue of the hymenopterous insects in the collection of the British Museum. Part VI. Formicidae. + + + +Author + +Smith, F. + +text + +1858 +British Museum + +London + + + +http://antbase.org/ants/publications/8127/8127.pdf + +book +8127 +C86CFDBF-61D9-48EE-9C2E-325FC0462B10 + + + + +Genus +MYRMECOCYSTUS +. + + + + +Myrmecocystus +, Wesm. Bull. Acad. Roy. de Brux. v. (1838) p. 766. + +Lucas, Bull. Ent. pl. 54; Ann. Soc. Ent. Fr. (1855). + + +" The first abdominal segment of one node; the mandibles triangular and much toothed; abdomen swollen at times like a balloon, and then perfectly transparent. In Mexico called hor- migas micleras or mochileras, i. e. honey-ants or pouched ants. their abdomen containing a sufficiently agreeable honey." + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D305FFA2FF27ED6627E81D9F.xml b/data/38/7F/30/387F3068D305FFA2FF27ED6627E81D9F.xml new file mode 100644 index 00000000000..7da07a2f364 --- /dev/null +++ b/data/38/7F/30/387F3068D305FFA2FF27ED6627E81D9F.xml @@ -0,0 +1,200 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +5.1. Genus + +Aploploides +Rehn & Hebard, 1938 + + + + + +Type-species: + +Aploploides stenocephalum +Rehn & Hebard, 1938 +: 49 + +, by original designation of +Rehn & Hebard, 1938 +: 49. + + + + + +Aploploides +Rehn & Hebard, 1938 +: 49 + +. + + +Bradley & Galil, 1977 +: 188. +Moxey, 1972 +: 54 (in litt.). +Bragg, 2001 +: 628. + + +Zompro, 2004 +: 305. + + +Otte & Brock, 2005 +: 49. + + + + + +Description: ♀♀, ♂♂ ( +Figs. 53–54 +). + +Rather small, elongate and slender Haplopodini (body lengths: ♂♂ 73.0–78.0 mm, ♀♀ 87.6–95.0 mm), ♂♂ with fully developed alae, ♀♀ apterous. Body subcylindrical with entire surface smooth and shiny (except for very minute granules on the vertex, pronotum and along lateral margins of the mesonotum). General colouration greenish. Head elongate, +2x +longer than wide, vertex flat and smooth; cheaks gently widened ( +Fig. 58 +). Eyes small, subcircular. Antennae filiform, longer than head and complete thorax combined in ♂♂, shorter than head, pro and mesonotum combined in ♀♀. Scapus dorsoventrally compressed, pedicellus subcylindrical. Pronotum slightly shorter and narrower than head, rectangular. Mesothorax elongate, about 1.5x longer than head and pronotum combined. Mesonotum parallel-sided and with a fine longitudinal median carina. Mesosternum simple. Metanotum rectangular. Meso- and metapleurae unarmed. Tegmina of ♂♂ small and scale-like, alae reaching about half way along tergum VI. Anal region transparent. Median segment rectangular and slightly longer than metanotum. Abdomen elongate. Segments II–VI of ♂♂ parallel-sided, of equal width and about +3x +longer than wide; of ♀♀ just slightly longer than wide. Segment VII of ♀♀ longer than previous and slightly narrowing towards the posterior, VIII–X shorter than previous and tapering to apex. Sternum VII of ♀♀ with a faint praeopercular organ, formed by a median tubercle close to posterior margin. Anal segment of ♂♂ with a faint posteromedian indentation, of ♀♀ bilobate. Epiproct very small, triangular. Cerci slender, elongate, very weakly incurving and tapered towards the apex ( +Figs. 55–56 +). Poculum of ♂♂ indistinct and scooplike, just reaching posterior margin of tergum IX ( +Fig. 57 +), posterior with a slight median indentation. Vomer broadly triangular, somewhat narrowed in apical half and with a short and blunt terminal hook ( +Fig. 344 +). Subgenital plate of ♀♀ elongate, keeled and extending beyond apex of abdomen by about 2/5 of its total length, apex slightly rounded ( +Figs. 55–56 +). Legs of moderate length in ♂♂, and comparatively short in ♀♀ the profemora being shorter than the mesonotum and hind legs (incuding tarsi) reaching to posterior of tergum VI. Profemora strongly compressed and curved basally, with the medioventral carina slightly displaced towards anteroventral carina. Medioventral carina of meso- and metafemora minutely spinulose, anteroventralcarina bispinose subapically. Basitarsi short, at most as long as combined length of following two tarsomeres, simple. Eggs unknown. + + +Differentiation: +Easily distinguished from all other genera of Haplopodini by the following characters: head elongate +2x +longer than wide vertex flat and smooth; antennae of ♀♀ shorter than head and thorax combined; body surface entirely smooth and glabrous (except for very minute granules on the vertex, pronotum and along lateral margins of the mesonotum); legs very weakly armed; ♀♀ apterous. + + +The lack of wings in ♀♀ is shared with the Cuban + +Venupherodes + + +n. gen. + +and Jamaican + +Paracranidium +Brock, 1998 + +, but the first genus differs at once by the globose and bi-cornute head, and the latter by the triangular crosssection of the body and prominent, semicircularly raised median keel of the mesonotum. + + + + + +Distribution ( +Fig. 374 +): + +Northwest +Cuba +(Pinar del Rio Province), endemic. + + + + + +FIGURES 53–58. + +Aploploides stenocephalum +Rehn & Hebard, 1938 + +. +53. +♀ PT: NW-Cuba, Pinar del Rio [ANSP]; 54. ♂ PT: NW-Cuba, Pinar del Rio [ANSP]; +55. +♀ apex of abdomen, lateral view; +56. +♀ apex of abdomen (dorsal view); +57. +♂ apex of abdomen (lateral view); +58. +♀ PT head in lateral view: Cuba, Pinar del Rio [ANSP]. + + + + + + +Species included: + + + +1. + +Aploploides stenocephalum +Rehn & Hebard, 1938 +: 49 + +, pl. 4: 18–21 (♂, ♀). + + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D306FFA3FF27EECF27F21A8D.xml b/data/38/7F/30/387F3068D306FFA3FF27EECF27F21A8D.xml new file mode 100644 index 00000000000..c8c7158f2cf --- /dev/null +++ b/data/38/7F/30/387F3068D306FFA3FF27EECF27F21A8D.xml @@ -0,0 +1,212 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +5.2. Genus + +Apteroplopus + +n. gen. + + + + +Type-species: + +Dyme +grosse-tuberculata + +Brunner v. Wattenwyl, 1907: 323, by present designation. + + + + + +Dyme +, Brunner + +v. Wattenwyl, 1907: 318 (in part—not + +Dyme +Stål, 1875 + +). + +Bacteria +, +Otte & Brock, 2005 +: 64 + +(in part). + + + + + +Description: ♂♂ ( +Fig. 59 +). + +Large (body length +115.4 mm +) and very slender, apterous Haplopodini. Body surface strongly shiny and smooth except for some paired tubercles on the mesonotum and minute granules on the meso- and metapleurae. Head indistinctly longer than wide and gently narrowing towards the posterior, vertex very gently convex and with two small tubercles. Eyes prominent, circular and projecting hemispherical. Antennae conspicuously thickened and longer than head and complete thorax combined;> 50 antennomeres. Scapus 1.5x longer than wide, oval in cross-section. Pronotum rectangular and unarmed, slightly longer and as broad as head. Mesothorax very elongate, more than 3.5x longer than head and pronotum combined. Mesonotum parallel-sided and slightly broadened at the posterior, dorsally armed with several irregularly paired, blunt tubercles. Metanotum half the length of mesonotum, slightly broadened at +anterior +margin. Meso- and metasternum and pleurae simple, the latter very minutely granulose. Abdomen about as long as head and complete thorax combined. Median segment about ¼ the length of the metanotum. Abdominal segments II–VII slightly decreasing in length, at least 2.5x longer than wide and parallel-sided. Tergum +VIII 2 +/3 the length of VII, swollen and roundly dilated subapically; distinctly broader than II–VII and broadest segment. Posterior margin of anal segment with a wide concave excavation, the posterolateral angles thickened ( +Fig. 61 +). Cerci of moderate size, laterally compressed, slender, slightly incurving and tapered towards the apex; projecting over apex of anal segment ( +Figs. 60–61 +). Vomer distinct, triangular with a single terminal hook. Poculum moderately convex, scoop-like and with a slight posteromedian indentation; just reaching to posterior margin of tergum IX ( +Fig. 60 +). Legs long and slender, profemora and mesofemora shorter than mesothorax, hind legs almost reaching apex of abdomen. Profemora strongly compressed and curved basally, the meso- and metafemora very slightly constricted towards the base. Anterodorsal carina of meso- and metafemora slightly elevated sub-apically. Medioventral carina of profemora very indistinctly displaced towards anteroventral carina, with two minute teeth apically. Outer ventral carinae of meso- and metafemora with 2–4 sub-apical spines. Medioventral carina of meso- and metafemora with 3–4 spines sub-apically. Tibiae unarmed. Tarsi elongate, probasitarsus as long as following three tarsomeres combined with the dorsal carina slightly elevated towards the apex. Meso- and metabarsitarsi as long as following two tarsomeres combined. ♀♀ and eggs unknown. + + + + +Differentiation: +♂♂ are easily distinguished from all other genera of Haplopodini by lacking tegmina and alae, very elongate mesothorax which is more than 3.5x longer than the head and pronotum combined, and having the median segment considerably shortened, being less than 1/3 the length of the metanotum. Furthermore, this is the only representative of Haplopodini to be known from Central +America +. From the closely related + +Haplopus +Burmeister, 1838 + +♂♂ may additionally be distinguished by the smaller and more slender, laterally compressed and apically tapered cerci. + + + + +Comments: + +Dyme +sensu Brunner + +v. Wattenwyl (not +Stål, 1875 +) is a highly polyphyletic grouping and examination of his specimen of + +D. grossetuberculata + +has shown this clearly not to be a member of + +Dyme +Stål, 1875 + +. The glabrous body surface, conspicuously thickened antennae, apically spinose ventral carinae of the femora, slightly displaced medioventral carina of the profemora, tuberculate mesonotum as well as features of the genitalia place this species in the tribe Haplopodini. Features such as the complete lack of tegmina or alae, short median segment and very elongate mesothorax clearly show it to form a distinct generic unit, here named + +Apteroplopus + + +n. gen. + +. Within Haplopodini the new genus appears to be close to + +Haplopus +Burmeister, 1838 + +, showing strong general resemblance to ♂♂ of this genus. + + + + + +Distribution ( +Fig. 377 +): + +Honduras +. + + + + +Etymology: +Masculine. A combination of “ +Apterus +” (lat. = wingless) and the ending “- +plopus +” to indicate the close relation to + +Haplopus +Burmeister, 1838 + +. + + + + + + + +Species included: + + + +1. + +Apteroplopus +grosse-tuberculatus + +(Brunner v. Wattenwyl, 1907: 323) [ + +Dyme + +]. + + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D307FFA2FF27EF43260519C1.xml b/data/38/7F/30/387F3068D307FFA2FF27EF43260519C1.xml new file mode 100644 index 00000000000..3feb7587aa6 --- /dev/null +++ b/data/38/7F/30/387F3068D307FFA2FF27EF43260519C1.xml @@ -0,0 +1,249 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Aploploides stenocephalum +Rehn & Hebard, 1938 + + + + + +( +Figs. 53–58 +, +334 +, +352 +, +374 +) + + + + + + +Aploploides stenocephalum + +Rehn & Hebard, 1938 +: 49 + + +, pl. 4: 18–21 (♂, ♀). +HT +, ♂: +Cuba +, Pinar del Rio, Pinar del Rio Province, +Sept. 14 +’ +13 F. +E. Lutz, five kilometers distand on road to Coloma, river edge, area of bamboo, shrubs and Weeds; + +Aploploides stenocephalum + +R + H, +Holotype +[USNM]; +AT +, ♀: +Cuba +, 12 ½ K. S. of Pinar Rio, +Sept. 23 +’13, F.E. Lutz, region of pines and palmettos, taken from pine, + +Aploploides stenocephalum + +R + H, Allotype [USNM]; +PT +, 1 ♀: +Cuba +, 12 ½ K. S. of Pinar Rio, +Sept. 23 +’13, F.E. Lutz, region of pines and palmettos, taken from pine, + +Aploploides stenocephalum + +R + H, +Paratype +[USNM]; +PT +, ♂: +Cuba +, 12 ½ K. S. of Pinar Rio, +Sept. 23 +’13, F.E. Lutz, region of pines and palmettos, taken from pine, + +Aploploides stenocephalum + +R + H, +Paratype +[USNM]; +PT +, ♀: +Cuba +, 12 ½ K. S. of Pinar Rio, +Sept. 12–23 +’13, + +Aploploides stenocephalum + +R + H, +Paratype +, w0090, ANSP [ANSP]; +PT +, ♂: + +Aploploides stenocephalum + +R + H, +Paratype +Hebard CLN, +Cuba +/3., K. S. of Pinar Rio, +Sept. 12–23 +’13, w0091, ANSP [ANSP]; +PT +, ♂: + +Aploploides stenocephalum + +R + H, +Paratype +Hebard CLN, +Cuba +/3., K. S. of Pinar Rio, +Sept. 12–23 +’13, w0092, ANSP [ANSP]. + +Moxey, 1972 +: 55 + +, fig. 11 (♀ anal segment; in litt.). + +Otte & Brock, 2005 +: 49 + +. + + + + + + + + +Further material [ +1 ♂ +, 3 nymphs]: + + + + +CUBA +: + + +1 ♂ +: Col. F. de Zayas, Pinares de Vinales, +V.1960 +, Prov. P.R. +CUBA +[ +USNM +]; +1 ♂ +(penultimate instar), 2 nymphs: +Cuba +, Cerro de Cabras ca. +400 ft +., Pinar del Rio Province, +Sept. 11 +’13, C.W. Leng, beaten from pine in a dense forest [ +USNM +]. + + + + +Comments: +The original descriptions of +Rehn & Hebard (1938) +are very detailed and along with the illustrations provided (pl. 4, figs. 18–24) serve well to recognize this distinctive species. Furthermore, the diagnosis of the genus presented above is sufficient enough for differentiation. Hence, no descriptions are provided. The +holotype +has the terminal abdominal segments destroyed by pests. + + + + + +Distribution ( +Fig. 374 +): + +Western +Cuba +(Pinar del Rio Province: Pinar del Rio [ANSP; USNM]; Cerro de Cabras [USNM] & Pinares de Viñales [USNM]). + + + + +Number of specimens examined: +11 + + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D308FFAFFF27EDBA26761AA8.xml b/data/38/7F/30/387F3068D308FFAFFF27EDBA26761AA8.xml new file mode 100644 index 00000000000..8c2f3f14cb5 --- /dev/null +++ b/data/38/7F/30/387F3068D308FFAFFF27EDBA26761AA8.xml @@ -0,0 +1,527 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +5.3. Genus + +Cephaloplopus + +n. gen. + + + + +Type-species: + +Cephaloplopus pulchellus + + +n. sp. + +, by present designation. + + + + +Description: +♂♂, ♀♀. Small to medium-sized (body length including subgenital plate ♀♀ +84.5–88.9 mm +, ♂♂ +58.2–72.4 mm +) and moderately elongate Haplopodini. ♀♀ brachypterous, ♂♂ brachypterous or with fully developed alae. Body ± cylindrical (♂♂) or sub-cylindrical (♀♀) in cross-section. Colouration of ♀♀ various shades of brown, straw and grey. ♂♂ colourful and multi-colourous insects, mostly pale to dull green with body surface glabrous. Head indistinctly longer than wide and globose, vertex roundly convex and distinctly bi-cornute. Horns extending by> 2/3 the height of head capsule, sometimes with a single point only (certain ♂♂) but usually crenate or multi-tuberculose; the dextral horn larger than the sinistral. Antennae filiform in ♀♀ and moderately thickened and robust in ♂♂; in ♀♀ almost as long as head and complete thorax combined, in ♂♂ reaching at least to abdominal segment III. Pronotum slightly shorter than the head and with a ± distinct pair of +anterior +tubercles or spines (rarely with an additional posterior pair); otherwise smooth (♂♂) or tuberculose (♀♀). Mesothorax elongate and ± parallel-sided, at least +2x +longer than head and pronotum combined. Mesonotum in ♀♀ rather irregularly and to a various degree armed with granules and spiniform tubercles, in ♂♂ armed with 6–10 ± distinct and pointed spines. Mesopleurae smooth in ♂♂ and with a longitudinal row of acute granules in ♀♀. Meso- and metasternum irregularly and sparsely granulose in ♀♀, the metasternum smooth in ♂♂. Tegmina broadly oval and with a moderately distinct central hump; ± reaching to (♀♀) or projecting over posterior margin of metanotum (♂♂). Alae of ♀♀ ± as long as tegmina; of ♂♂ variable, either indistinctly longer than tegmina or as long as reaching to abdominal segment VI. Anal region reticulate with distinct brown to black radial and transverse veins in ♀♀, translucent pink in ♂♂ and with only the marginal portion reticulate. Abdomen considerably longer than head and thorax combined. Median segment longer than metanotum, smooth. Segments II–VII longer than wide (more distinct in ♂♂). Tergites unarmed in ♂♂, II–IV often with a ± prominent pair of spines or crenate posterior lobes in ♀♀. VII with lateral margins widely expanded and forming a prominent lobe which laterally extends by> ½ the width of body; posterior margin irregularly dentate in ♀♀. VIII–X slightly narrower (♀♀) or roughly equal in width (♂♂) to previous segments. Sternites II–VII smooth in ♂♂ and with a few small granules in ♀♀. Praeopercular organ of ♀♀ formed by a distinct elongate, wart-like median tubercle close to posterior margin of sternum VII. Anal segment with a longitudinal median carina, the posterior margin tapered and with a slight median notch. Epiproct very small, roundly triangular and hardly projecting over posterior margin of anal segment. Vomer of ♂♂ well developed, the basal portion roundly broadened and the terminal hook of moderate length. Cerci tapered towards the apex and laterally compressed, very small in ♀♀ and about 2/3 the length of anal segment in ♂♂. Poculum of ♂♂ convex, cup-like and longitudinally carinate. Subgenital plate of ♀♀ rather moderately elongate, projecting over the apex of abdomen by more than the length of tergum X (anal segment) and with the apex rounded. Legs of moderate length, profemora shorter (♀♀) or slightly longer than mesothorax (♂♂), mesofemora shorter (♀♀) or about as long as mesothorax, and hind legs not (♀♀) or ± reaching to apex of abdomen (♂♂). Two outer ventral carinae of meso- and metafemora each with 1–3 sub-apical spines or teeth, the medioventral carina of these femora with a longitudinal row of 4–6 ± distinct spines. The outer ventral carinae of ♀♀ sometimes elevated into rounded lobe (occasionally dentate). Dorsal carinae of all femora unarmed, but sometimes with a ± distinct, roughly triangular sub-apical tooth on the posterior carina in (♂♂). ♀♀ with a ± prominent sub-apical lobe on posterodorsal carina, the meso- and metafemora each with a ± prominent sub-apical and sub-basal lobe (the sub-basal lobes may be very shallow). Tibiae unarmed in ♂♂ and with 1–4 rounded dorsal lobes in ♀ (the basal lobe always present and largest). Coxae spinose. All basitarsi elongate and longer than following three tarsomeres combined; probasitarsus of ♀♀ with a rounded lobe dorsally. + + +Eggs: +Small (capsule length +3.1–3.4 mm +), barrel-shaped and cylindrical in cross-section; capsule about 2.0x longer than wide. Dorsal surface of capsule considerably more convex than ventral surface. Polar-area ± impressed. Capsule surface strongly coriaceous and covered with irregular raised tubercles and ridges. Micropylar plate variable in shape, basal portion broadened and <½ the length of capsule; sculptured like capsule. Posterior end of micropylar plate with a distinct triangular gap. Median line short but distinct. Operculum flat, circular and in the centre structured like capsule; no conspicuous central capitulum. Colouration brown. + + + + + +Differentiation ( +Table 5 +): + +Closely related to + +Haplopus +Burmeister, 1838 + +but readily distinguished by: the considerably smaller size (body lengths: ♀♀ < +100 mm +, ♂♂ < +70 mm +); very prominent horns of the head which extend by> 2/3 the height of the head capsule; shorter mesothorax; large lateral lobes of abdominal tergum VII of both sexes; more prominently lobate legs and lobed probasitarsus of ♀♀; smaller, laterally compressed and tapered cerci of ♂♂. The eggs are remarkably different by having the capsule surface decidedly tuberculose, the capsule indented at the polar-area and lacking a knob-like capitulum. For a more detailed comparison and differentiation see +Table 5 +below. + + + + + +Distribution ( +Fig. 377 +): + +Hispaniola & +Cuba +. + + + + +Etymology: +Masculine. The generic name is a combination of “ + +Cephalus + +” (lat. = head), which draws emphasise to the prominent head armature, and the ending “- +plopus +” to indicate the close relation to + +Haplopus +Burmeister, 1838 + +. + + + + + + + +Species included: + + + +1. + +Cephaloplopus alope + + +n. sp. + +[Distribution: +Cuba +] 2. + +Cephaloplopus euchlorus + + +n. sp. + +[Distribution: Hispaniola] 3. + +Cephaloplopus laetus + + +n. sp. + +[Distribution: Hispaniola] 4. + +Cephaloplopus pulchellus + + +n. sp. + +[Distribution: Hispaniola] +......continued on the next page +Note: +The distinguishing features define to adult insects only. Nymphs of + +Haplopus + +spp. may have the body and leg armature considerably stronger developed than the corresponding adults, thus resembling + +Cephaloplopus + + +n. gen. + + + + + + +TABLE 5. +Comparison and differentiation of + +Cephaloplopus + + +n. gen. + +and + +Haplopus +Burmeister, 1838 + +. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+ +Cephaloplopus +n. gen. + + + +Haplopus + +
+Body length (♂♂) +<70 mm> 85mm
+Body length incl. subgen. pl. (♀♀) +<100 mm> 110 mm
+Antennae (♀♀) +Slender and filiformRobust
+Spines of the vertex +Very prominent; spine-like, conical, crenate or multi-tuberculate and extending by>2/3 the height of head capsuleSmall to moderately sized, with a single point; extending by <2/3 the height of head capsule
+Mesothorax (♀♀) +About 2x longer than head and pronotum combined> 2.2x longer than head and pronotum combined
+
+ + +TABLE 5. +(Continued) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+ +Cephaloplopus +n. gen. + + + +Haplopus + +
+Abdominal tergum VII +With very large posterolateral lobes, which extend by more than ½ the body widthAt best with small posterolateral lobes
+Cerci (♂♂) +Laterally compressed and tapered towards apex; at best 2/3 the length of anal segmentObtuse and ± cylindrical; about as long as anal segment
+Probasitarsus (♀♀) +With a rounded dorsal lobeSlender
+Profemora (♀♀) +With a ± prominent sub-apical lobe on posterodorsal carinaUnarmed dorsally
+Meso- and Metafemora (♀♀) +With a ± prominent sub-basal and sub-apical lobe on dorsal carinae (basal ones may be indistinct)At best with a slight sub-apical tooth on posterodorsal carina
+Tibiae (♀♀) +With 1–4 rounded dorsal lobesNot distinctly lobed
+Egg (capsule) +Barrel-shapedOvoid
+Egg (capsule surface) +Distinctly coriaceous / tuberculose and covered with irregular ridgesMinutely granulose / rugulose to almost smooth
+Egg (polar area) +ImpressedConvex and rounded
+Egg (micropylar plate) +At best ½ the length of capsule> ½ the length of capsule
+Egg (operculum) +Flat and with an irregularly raised circle of tubercles± convex; with a conical or knob-like central capitulum
+Distribution +Hispaniola & Cuba (Fig. 377)Hispaniola, Jamaica, Puerto Rico, Virgin Islands, Bahamas, Florida Keys, Cayman Islands 6 Swan Islands (Fig. 376)
+
+ + + + + +Keys to the species of + +Cephaloplopus + +n. gen. + + + + +♀♀* + + + + +1. Subgenital plate long and lanceolate, extending over abdomen by at least combined length of tergites IX–X; horns of the head flattened apically; Hispaniola............................................................................ 2 + + + +- Subgenital plate extending over abdomen by slightly more than length of anal segment ( +Figs. 64–65 +); horns of head distinctly conical ( +Fig. 63 +); +Cuba +........................................................................ + +alope + + +n. sp. + + + + + + + +2. Pronotum with two pairs of spines ( +Fig. 88 +); meso- and metafemora with prominent dorsal lobes sub-basally; tibiae with one rounded pre-medial lobe dorsally............................................................. + +pulchellus + + +n. sp. + + + + + +- Pronotum with one +anterior +pair of tubercles ( +Fig. 69 +); meso- and metafemora lacking dorsal sub-basal lobes; tibiae with at least two lobes dorsally..................................................................... + +euchlorus + + +n. sp. + + + + + + +* ♀♀ of + +C. laetus + + +n. sp. + +are not known + + +♂♂* + + + + +1. Alae well developed, exceeding abdominal tergum V......................................................... 2 + + + +- Brachypterous, alae reaching only half way along median segment ( +Figs. 80, 82 +).......................... + +laetus + + +n. sp. + + + + + + +2. Pronotum with two pairs of tubercles/spines ( +Fig. 89 +); general colouration dull green, head unicolorous ( +Fig. 89 +); costal region of alae with a longitudinal row of 6–8 distinct, elliptical pale spots ( +Fig. 86 +)........................... + +pulchellus + + +n. sp. + + + +- Pronotum with one +anterior +pair of tubercles ( +Fig. 70 +); general colouration pale green to cream; head pale green anteriorly, white posterolaterally and with a pale brown, longitudinal median stripe ( +Fig. 70 +); costal region of alae without a row of pale spots ( +Figs. 67–68 +)....................................................................... + +euchlorus + + +n. sp. + + + +* ♂♂ of + +C. alope + + +n. sp. + +are not known + + + +
+
\ No newline at end of file diff --git a/data/38/7F/30/387F3068D309FFADFF27EDC226091D9B.xml b/data/38/7F/30/387F3068D309FFADFF27EDC226091D9B.xml new file mode 100644 index 00000000000..b0eb6a91fe9 --- /dev/null +++ b/data/38/7F/30/387F3068D309FFADFF27EDC226091D9B.xml @@ -0,0 +1,160 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Apteroplopus grossetuberculatus + +(Brunner v. Wattenwyl, 1907) n. gen., n. comb. + + + + +( +Figs. 59–61 +, +377 +) + + + + + +Dyme +grosse-tuberculata + +Brunner v. Wattenwyl, 1907: 323. +HT +, ♂: Coll. Br. v. W.; +Honduras +, E. Wittkugel; det. Br. v. W. + +Dyme grossetuberculata + +; 18.563 [NHMW, No. 647]. + + + + + + +Bacteria grossetuberculata +, + +Brock, 1998a +: 32 + + +. + + + +Otte & Brock, 2005 +: 64. + + + + + +Description: ♂ ( +Fig. 53 +). + +The following description is based on the unique ♂ HT in NHMW, which is complete except for lacking the left hind claw and the terminal antennomeres of both antennae. + + +Large (body length +115.4 mm +) and very slender insect. General colouration plain mid to olive green, the abdomen slightly darker (brown in the HT due to preservation). Pronotum pale brown, the terminal three abdominal segments greyish brown. Antennae pale brown dorsally and black ventrally. Apices of all femora and tibiae dark brown. Tarsi reddish brown. Points of the mesonotal tubercles and leg armature bright green. Eyes dark reddish brown. + + +Head: Subcylindrical, vertex very gently convex and unarmed except for two minute tubercles. Eyes large, circular, their length only about 1.3x in that of cheeks. Scapus 1.5x longer than wide, slightly dorsoventrally compressed and oval in cross-section. Pedicellus cylindrical and 2/3 the length of scapus. Third antennomere almost twice as long as pedicellus; IV very short, V +2x +longer than VI. Following six antennomeres elongate and increasing in length (X longest), the remaining gradually decreasing in length towards tip of antennae. + +Thorax: Pronotum about 1.4x longer than wide and unarmed, transverse median depression distinct, slightly curved and almost reaching lateral margins of segment. Mesonotum parallel-sided and slightly broadened at the posterior. Dorsal surface armed with about 16 irregularly paired, blunt tubercles which decrease in size towards the posterior. Meso- and metapleurae with a longitudinal row of small, rounded granulose. Meso- and metasternum simple. + +Abdomen: Median segment about 1.7x longer than wide and gently constricted medially. Tergum VIII dorsally with three almost parallel, longitudinal carinae. IX about 2/3 the length of VIII, distinctly narrower, decidedly constricted medially and with a blunt longitudinal dorsal keel. Anal segment less than ¾ the length of IX, gently widened towards the posterior and with a wide roughly triangular median excavation; dorsally with a fine longitudinal median carina ( +Fig. 61 +). + +Legs: As for the genus. + + + +Comments: +♀♀ and eggs unknown. So far only known from the unique ♂ +holotype +( +Fig. 55 +). + + + + + +Distribution ( +Fig. 377 +): + +Honduras +[NHMW]. + + +Number of specimens examined: +1 + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D30DFFA9FF27EAFF26091A67.xml b/data/38/7F/30/387F3068D30DFFA9FF27EAFF26091A67.xml new file mode 100644 index 00000000000..38c10238b33 --- /dev/null +++ b/data/38/7F/30/387F3068D30DFFA9FF27EAFF26091A67.xml @@ -0,0 +1,283 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Cephaloplopus alope + +n. gen. +, n. sp. + + + + +( +Figs. 62–65 +, +335 +) + + + + + + +Diapherodes alope + +Moxey, 1972 +: 92 + + +(in litt.). [Nomen nudum] + + + + + +HT, +♀: Camagüey, +Cuba +, +July 30. 1923 +, J. Acuña Col., E.E.A. +Cuba +; Ento No. 10660, w0179, + +Diapherodes alope +Moxey + +Type +(MS) [ANSP]. + + +PT, +♀ (nymph): E.E.A. +Cuba +, Ento No. 10680, w0184, + +Diapherodes alope +Moxey + +Paratype +(MS) [ANSP]. + + +PT, +♀ (nymph): E.E.A. +Cuba +, Ento No. 10681, w0182, + +Diapherodes alope +Moxey + +Paratype +(MS) [ANSP]. + + +PT, +♀ (nymph): E.E.A. +Cuba +, Ento No. 10682, w0181, + +Diapherodes alope +Moxey + +Paratype +(MS) [ANSP]. + + +PT, +♀ (nymph): Camagüey, +Cuba +, Col. J. Acuña, Julie 21. 1923, E.E.A. +Cuba +, Ento No. 10660, w0183, + +Diapherodes alope +Moxey + +Paratype +(MS) [ANSP]. + + +PT, +♀ (nymph): Cangrejeras, Prov. Habana, +May 30 +,´31, S.C. Bruner, w0180, + +Diapherodes alope +Moxey + +Paratype +(MS) [ANSP]. + + + + +Diagnosis: +This, the only Cuban species of the genus, is distinguished from the three other known members by the distinctly conical horns of the head, which are almost circular in cross-section ( +Fig. 63 +), and much shorter subgenital plate, which projects over the apex of the abdomen by only a little more than the length of the anal segment ( +Figs. 64–65 +). Furthermore, the lobes of the legs are comparatively less developed. + + + + +Etymology: +“ + +Alope + +” was the beautiful daughter of King Cercyon, and is a noun in apposition to the generic name + +Haplopus + +. It is the manuscript name supposed for this species by +Moxey (1972: 92, in litt.) +and here selected. + + + + + +Description: ♀ ( +Fig. 62 +). + +Of moderate size (body length incl. subgenital plate 85.0– +88.9 mm +) and rather slender for the genus, with a pair of very prominent conical cephalad horns, a greatly triangularly dilated abdominal tergum VII and comparatively short subgenital plate. General colouration of body and legs reddish to ochraceous mid brown with a greyish wash and all over furnished with pale grey to whitish speckles and markings, the legs with irregular dark greyish brown markings. Eyes dull red, antennae except scapus reddish brown. Tegmina and costal region of alae very dark brown and mottled with some pale green. Anal region of alae red with darker veins. Tarsi chestnut brown. + + +Head ( +Fig. 63 +): Strongly globose, vertex convex and armed with an extremely prominent pair of large conical horns (the dextral one about +3x +larger than the sinistral), which extend by as much as the height of head capsule; horns cylindrical basally carinate apically and tipped with a minute spine at the apex. Remainder parts of head with scattered, minute tubercles. Between the bases of the antennae with a slightly raised and smooth oval area. Eyes rather small, circular and conatined about 2.5x in length of cheeks. Antennae at least as long as complete thorax and median segment combined (broken in the HT). Scapus oval in cross-section, rectangular, +2x +longer than wide. Pedicellus cylindrical and less than half the length of scapus. + + +Thorax: Pronotum considerably shorter and narrower than head, longer than wide and slightly narrowing posteriorly. Transverse median sulcus indistinct and short, not reaching lateral margins of segment. +Anterior +half with a pair of strong spine-like tubercles ( +Fig. 63 +), posterior margin with four regularly-spaced tubercles, remaining parts of pronotum very minutely granulose. Mesothorax about +2x +longer than head and pronotum combined. Mesonotum covered with numerous scattered small tubercles and four conspicuous tuberculate spines clustered close to the +anterior +margin ( +Fig. 63 +) as well as a few slightly larger tubercles medially. Meso- and metapleurae as well as meso- and metasternum with a few scattered small tubercles. Tegmina oval, scale-like and narrowed towards the base, just reaching to posterior margin of metanotum; central protuberance shallow. Alae shorter than tegmina and reaching less than half length along median segment. + + +Abdomen: Median segment roughly +2x +longer than wide and widened towards the posterior margin; unarmed. Segments II and III of equal length and width, parallel-sided. IV–VI slighly tapering and decreasing in length, VI shortest and narrowest, VII as long as II. II–VI on average about +2x +longer than wide. Tergites II and III each with a pair of retrorse posteromedial spines and on each side with a prominent, foliaceous, triangular elevation (largest on II). IV with four minute retrorse spines at posterior margin, V and VI unarmed. VII with four irregular, raised longitudinal carinae and greatly dilated towards the posterior, forming a roughly triangular, foliaceous lateral expansion, which laterally projects by more than 2/3 of body width ( +Fig. 64 +). Sternites II–VII unarmed. Praeopercular organ formed by two gently curved and somewhat converging carinae at posterior margin of sternum VII ( +Fig. 335 +). Tergum +VIII 2 +/3 the length of VII, distinctly narrower, strongly convex, parallel-sided and 1.3x longer than wide; +anterior +margin broader than posterior margin; +IX 2 +/3 the length of VIII. Anal segment very slightly shorter than IX, tapered towards the apex, posterior margin with a shallow concave excavation ( +Fig. 64 +). Epiproct distinct, triangular, tectiform and projecting over posterior margin of anal segment ( +Fig. 64 +). Cerci short, oval in cross-section and tapered towards the apex, finely setose. Subgenital plate fairly short, slightly keeled with the apex rounded and projecting over apex of abdomen by slightly more than length of anal segment ( +Figs. 64–65 +). + + +Legs: Profemora ¾ length of mesothorax, mesofemora slightly longer than metathorax and metafemora reaching about 1/3 the way along abdominal segment IV. Medioventral carina of profemora unarmed, of mesofemora with 2–3 and of metafemora armed with 3–5 spines. Antero- and posteroventral carinae of meso- and metafemora each with two small triangular sub-apical teeth. Dorsal carinae of meso- and metafemora with a minute and blunt submedial tooth and a more distinct tooth sub-apically (that of the +anterior +carina considerably larger). All tibiae unarmed except for a minute, rounded lobe about ¼ the way along anterodorsal carina. Basitarsi slightly longer following three tarsomeres combined, dorsal carina of probasitarsus just gently rounded. + + +Nymphs: +These are similar in appearance and colour to the adult insects but have the armature of the thorax, abdomen and legs much more prominently developed. + + + + +Comments: +Moxey (1972: 92) +described + +Diapherodes alope + +in manuscript but never published this name. The suggested type-material and specific name are taken from Moxey. The ♀ from Alianza in ANSP and considered a PT by Moxey is not traced. + + + + +Distribution: +Cuba +(Camagüey & Province Habana: Cangrejeras) [ANSP]. + + + + +Number of specimens examined: +6 + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D30FFFB6FF27ED8E21E51AA4.xml b/data/38/7F/30/387F3068D30FFFB6FF27ED8E21E51AA4.xml new file mode 100644 index 00000000000..657c5910b51 --- /dev/null +++ b/data/38/7F/30/387F3068D30FFFB6FF27ED8E21E51AA4.xml @@ -0,0 +1,511 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Cephaloplopus euchlorus + +n. gen. +, n. sp. + + + + +( +Figs. 66–79 +, +336 +, +353 +, +379 +) + + + + +HT +, ♂: +Dominican Republic +, RD-063 Sierra Prieta, Santo +Domingo +Prov., +18°38.315’N +69°58.302’W +, +20.XI.2002 +, D. Perez, R. Bastardo, B. Hierro [USNM]. + + +PT, +♀: +Dominican Republic +, RD-063 Sierra Prieta, Santo +Domingo +Prov., +18°38.315’N +69°58.302’W +, +20.XI.2002 +, D. Perez, R. Bastardo, B. Hierro [USNM]. + + +PT, +egg (ex abdomen): +Dominican Republic +, RD-063 Sierra Prieta, Santo +Domingo +Prov., +18°38.315’N +69°58.302’W +, +20.XI.2002 +, D. Perez, R. Bastardo, B. Hierro [USNM]. + + +PT, +♂: +Dominican Republic +, RD-041, Sierra Prieta, Villa Mella, Santo +Domingo +Prov., +18°38.939’N +69°58.373’W +, + +8.VII. +2002 + +, 500 ft., D. Perez, B. Hierro, R. Bastardo [USNM]. + + +PT, +♂: +Dominican Republic +, RD-219 Sierra Prieta, Villa Mella, Santo +Domingo +Prov., +142 m +, +18°38.925’N +69°58.303’W +, +12.IV.2004 +, D. Perez, B. Hierro, R. Bastardo. (n) [USNM]. + + +PT, +♀ (penultimate instar): +Dominican Republic +, RD-091, Sierra Prieta, Santo +Domingo +Prov., +133 m +, +18°39.010’N +69°58.409’W +, +18.III.2003 +, D. Perez, R. Bastardo, B. Hierro (night) [USNM]. + + +PT, +♀ (nymph n3): +Dominican Republic +, RD-063, Sierra Prieta, Santo +Domingo +Prov., +18°38.315’N +69°58.302’W +, +20.XI.2002 +, D. Perez, R. Bastardo, B. Hierro [USNM]. + + +PT, +♀ (nymph n4): +Dominican Republic +, DR-062 ~ +5 km +W Las Américas Airport, Santo +Domingo +, +18°28.158’N +69°43.601’W +, +19.XI.2002 +, D. Perez, R. Bastardo, B. Hierro. (night) [USNM]. + + +PT, +♀ (nymph n2): +Dominican Republic +, DR-060 Monte Rio, ~ +4 km +W of beach, +70 m +, dry scrub, +18°22.972’N +70°43.036’W +, +17.XI.2002 +, D. Perez, R. Bastardo, B. Hierro. (night) [USNM]. + + + + +Diagnosis: +Females differ from those of the the Cuban + +C. alope + + +n. sp. + +by: the longitudinal apical keel of the cephalad horns ( +Fig. 62 +); much longer subgenital plate, which projects over the abdomen by almost 1.5x the combined length of abdominal tergites IX–X ( +Fig. 68 +); dorsally multi-lobate protibiae and presence of a distinct dorsal sub-apical lobe on the meso- and metatibiae. Males are very similar to those of + +C. laetus + + +n. sp. + +but at once differ by the well developed alae ( +Fig. 67 +, hardly longer than the tegmina in + +laetus + +), but also by the more slender and brownish instead of green legs, more distinct sub-apical tooth of the dorsal carinae of the meso- and metafemora and shape of the anal segment ( +Fig. 70 +). + + +From + +C. pulchellus + + +n. sp. + +it differs by the shorter horns of the head ( +Figs. 62–63 +), lacking a posterior pair of tubercles on the pronotum and smaller lateral lobes of abdominal tergum VII of both sexes. ♀♀ also differ by: the longer alae; smaller crest-like lobes of abdominal tergum II ( +Fig. 65 +); lack of the lateral sub-basal lobes of the subgenital plate; lack of sub-basal dorsal lobes on the meso- and metafemora and presence of a rounded, dorsal sub-apical lobe on the meso- and metatibiae. Males furthermore differ by: the less angular anal segment ( +Fig. 70 +); pale green general colouration; pale brown legs and lack of distinct pale spots along the +anterior +margin of the costal region of the alae. The eggs can be distinguished from those of + +C. pulchellus + + +n. sp. + +by: the less distinctly sculptured capsule surface and narrow +anterior +extension of the micropylar plate ( +Figs. 71–72 +). + + + + +FIGURES 66–68. + +Cephaloplopus euchlorus + +n. gen. +, n. sp.. +66 +♀ PT: Dominican Republic, Santo Domingo Province, Sierra Prieta [USNM]; +67. +♂ HT: Dominican Republic, Santo Domingo Province, Sierra Prieta [USNM]; +68. +♂ PT: Dominican Republic, Santo Domingo Province, Sierra Prieta [USNM]. + + + + +Etymology: +The specific name “ + +euchlorus + +” (lat. = beautifully coloured) refers to the pretty colouration of the ♂♂, which consists of bright apple green, pale and dark brown, yellow and white. + + + + + +Description: ♀ ( +Fig. 66 +): + +Of moderate size for the genus (body length including subgenital plate +87.5 mm +) and rather slender, with a prominent pair of crenulate horns on the head, a moderately dilated abdominal tergum VII and comparatively long subgenital plate. General colouration of body and legs mid brown with a greyish wash and all over furnished with irregular whitish speckles and markings. Head with cheeks mostly white and a small, elongate black spot above eyes, a conspicuous dark brown marking near posterior margin. Eyes dark reddish brown, antennae greyish brown with indistinct blackish annulations. Tegmina and costal region of alae very dark brown with a green wash in central portion; the main longitudinal veins black. Anal region of alae bright red with all longitudinal veins broadly marked with black. + + +Head: Strongly globose, vertex convex and armed with a pair of prominent, apically compressed and crenulate cephalad horns (the dextral one almost +2x +larger than the sinistral); both lateral surfaces of the horns with several spiniform tubercles ( +Fig. 69 +). Posterior of vertex with a pair of moderate tubercles and a pair of minute granules on the frons. Eyes rather small, circular and contained a little more than +2x +in length of cheeks. Antennae reaching to posterior margin of mesonotum and consisting of about 45 segments. Scapus compressed dorsoventrally, roundly rectangular and about +2x +longer than wide. Pedicellus cylindrical and roughly half the length of scapus. + + +Thorax: Pronotum about as long but narrower than head, 1.2x longer than wide and gently constricted medially with the +anterior +margin widened and posterior margin rounded. Transverse median sulcus distinct and almost straight. +In anterior +portion with a pair of short spines ( +Fig. 69 +) and the surface otherwise with irregularly disposed small tubercles. Mesothorax about 2.2x longer than head and pronotum combined. Mesonotum with a fine longitudinal median carina and irregularly tuberculate; a cluster of four short but strong spines is present at +anterior +margin as well as two pairs of low spines in the median portion of the dorsal surface. The mesopleurae with a longitudinal row of about ten, the metapleurae with five small tubercles. Meso- and metasternum sparsely tuberculose. Tegmina oval, strongly broadened medially, narrowed towards the base and very slightly projecting over posterior margin of metanotum; central protuberance rather distinct, rounded. Alae reaching about 3/5 the way along median segment. + + +Abdomen: Median segment roughly +2x +longer than wide and widened towards the posterior; unarmed. Segments II–V roughly of equal length, VI slightly shorter than previous, III–VI gently narrowing; IV 3.3x longer than wide. Tergum VII slightly shorter than VI and with the lateral margin in posterior half dilated into a prominent rounded lobe, which laterally extends by about 2/3 the width of segment (broken in the unique adult ♀ available but described from a large ♀ nymph). All tergites with a few scattered granules and a longitudinal row of about five granules along lateral margins, II and III a pair of irregular, crenulate carinae posteromedial, which are less distinct on III ( +Fig. 72 +). These merely represented as a pair of tubercles on IV–IX. Sternites II–VI with a pair of short carinae near posterior margin and praeopercular organ represented by an elongate wart-like structure on VII ( +Fig. 336 +). Tergites VIII–X distinctly narrower than previous and roughly of uniform width; VIII ¾ the length of VII, almost +2x +longer than wide and gently constricted medially, +IX 2 +/3 the length of VIII. Anal segment shorter than IX, longitudinally carinate dorsally and with a concave lateral emargination; posterior portion strongly tapered towards a narrow and medially notched apex. Epiproct very small and with a posteromedian notch. Cerci short, conical and with a rather acute apex. Subgenital plate elongate, naviculate, keeled longitudinally and projecting over abdomen by more than the combined length of tergites IX–X ( +Fig. 75 +); apex rounded. + + +Legs: Profemora about ¾ length of mesothorax, mesofemora about as long as metathorax and metafemora slightly projecting over posterior margin of abdominal segment III. Medioventral carina of profemora with three spines, of meso- and metafemora with 4–5 rather strong spines. Posteroventral carina of meso- and metafemora with one, the anteroventral carina with two sub-apical spines; both carinae gently expanded and minutely dentate in basal portion. The dorsal carinae each with a roundly triangular lobe sub-apically. Anterodorsal carina of tibiae with a distinct rounded sub-basal and sub-apical lobe. The anterodorsal carina of profemora strongly raised, slightly undulate and with a small rounded lobe sub-apically; the same carina in protibiae furnished with 3–4 rounded lobes. Probasitarsus with a distinct rounded dorsal lobe and a little longer than following two tarsomeres combined ( +Fig. 71 +). Meso- and metabasitarsi slender and as long as following three tarsomeres combined. + + + +♂ ( +Figs. 67–68 +): + +Of moderate size (body length 63.8–72.0 mm) and rather slender for the genus with long alae (length 32.3–34.0 mm) which reach to abdominal segment VI; body surface glabrous. General colour of body pale creamish brown, the ventral body surface and three terminal abdominal segment pale apple green. Head creamish mid brown with the lower portions of cheeks white and the frons pale apple green. Antennae ochre with a greyish wash and with some grey annulations in apical portion. Eyes dark greyish brown with sepia mottling. Pronotum with the lateral margins broadly green. Lower portion of metapleurae and lateral margins of abdominal sternites II–V white. Spines of the mesothorax ochre with dark tips, lateral lobes of abdominal tergum VII dark brown, cerci creamish mid brown. Tegmina dark brown with the median portion of the +anterior +margin first pale green, then with a fine white stripe, the innermost portion pale apple green ( +Fig. 73 +). Costal region of alae with a similar green and interiorly white marking in basal portion, the +anterior +margin otherwise dull brown with slight pale mottling, then green; anal region transparent pale pink with a greyish wash along outer margin ( +Fig. 74 +). Legs and tarsi cream to mid brown with the apex of all femora slightly darker. + + + +FIGURES 69–79. + +Cephaloplopus euchlorus + +n. gen. +, n. sp.. +69. +Head of ♀ PT [USNM]; +70. +Head and pronotum of ♂ PT [USNM]; +71. +Protarsus of ♀ PT [USNM]; +72. +Abdominal tergum II of ♀ PT showing crenulate lobes [USNM]; +73 +Metathorax and tegmina of ♂ PT (lateral view) [USNM]; +74. +Right tegmen and ala of ♂ PT [USNM]; +75. +♀ PT, apex of abdomen (lateral view) [USNM]; +76. +♂ PT, apex of abdomen (lateral view) [USNM]; +77. +♂ PT, apex of abdomen (lateral view) [USNM]; +78. +Egg PT (dorsal view) [USNM]; +79. +Egg PT (lateral view) [USNM]. + + + +Head: General shape as in ♀♀ but with the cephalad horns even longer but not crenulate, apex compressed, carinate and with a single pointed spine; dextral horn projecting by> 2/3 the height of head capsule ( +Figs. 70 +). Surface otherwise smooth except for a posterior pair of tubercles. Eyes prominent, circular and projecting hemispherically, no more than 1.5x length of cheeks. Antennae ± reaching posterior margin of abdominal segment II; consisting of about 50 antennomeres. + + +Thorax: Pronotum about as long but narrower than head, general shape as in ♀♀. Surface smooth except for a pair of short spines in the +anterior +portion ( +Fig. 70 +). Mesothorax about 2.3x longer than head and pronotum combined. Armature of mesonotum variable; usually with four distinct, pointed spines near +anterior +margin ( +Fig. 70 +) and 2–3 pairs of pointed spines in the median portion. Meso- and metapleurae unarmed. Mesosternum with a few irregularly disposed granules, metasternum smooth. Tegmina oval and reaching about 1/3 along median segment, central protuberance distinct and roundly conical ( +Fig. 73 +). Alae reaching about 1/3 along abdominal segment VI. + + +Abdomen: Segments II–V of equal length and about 3.2x longer than wide; VI–VII slightly decreasing in length with VII no more than 2.3x longer than wide. All tergites and sternites smooth, sternites IV–VI with two low carinae near posterior margin. VII with lateral margins in posterior half expanded into a ± distinct roundly triangular and retrorse lobe ( +Figs. 76–77 +); this either indistinct or extending laterally by as much as 2/3 of body width. VIII slightly shorter than VII and gently constricted in basal portion; IX shorter than VIII and constricted medially. Anal segment with a faint longitudinal median carina and narrowed posteriorly, the posterior margin rounded on both sides of the triangular median emargination ( +Fig. 77 +), slightly swollen and on ventral surface armed with several small, black in-curving denticles. Vomer with base broadly semi-circular and the terminal hook rather long, papillate and gently up-curving ( +Fig. 353 +). Cerci elongate, a little longer than anal segment, slightly laterally compressed and gently incurving. Poculum moderately convex, cup-like, longitudinally carinate and with a blunt basal protuberance ( +Fig. 76 +). + +Legs: Profemora a little longer and mesofemora slightly shorter than mesothorax, metafemora reaching about half way along abdominal segment IV. Medioventral carina of profemora with 1–2 small sub-apical spines, of mesofemora with four and metafemora with five prominent, pointed spines. Dorsal carinae of meso- and metafemora with a ± distinct triangular sub-apical tooth or lobe (may be very faint). Basitarsi about as long as following three tarsomeres combined. + +Nymphs: +Even young nymphs show some of the characteristic features of this species, e.g. the crenulate cephalad horns or dorsal lobes of the tibiae. As in other species of the tribe, these have the whole body and leg armature much more prominently developed. The colouration includes various shades of brown furnished with a variable degree of whitish markings and speckles. + + +Variation: +In ♂♂ some variation is seen in the size of the cephalad horns, number and size of the mesonotal spines, size of the lateral lobe of abdominal tergum VII and size of the sub-apical tooth or lobe on the dorsal carinae of the meso- and metafemora. + + + +Egg ( +Figs. 78–79 +): + +Capsule +2x +longer than wide, surface sparsely covered with irregular tuberculate structures, sub-glabrous. Polar-area with a distinct indentation. Micropylar plate slightly less than half the length of capsule, almost +2x +longer than wide with the +anterior +1/3 strongly narrowed and the posterior portion rounded. Centre of micropylar plate with arounded, wart-like protuberance. Colour plain reddish mid brown. + +Measurements [mm]: Length 3.4, width 1.7, height 1.9, length of micropylar plate 1.6. + + + + +Distribution ( +Fig. 379 +): + +Hispaniola, S-Dominican Republic (Santo +Domingo +Province: Sierra Prieta & Azua Province: Monte Rio) [USNM]. + + + + +Number of specimens examined: +8 + + + +TABLE 7. +Measurements of + +Cephaloplopus euchlorus + + +n. gen. +, n. sp. + +[mm] + + + + + + + + + + + + + + + + + + + + + + + + + + + +
♂, HT [USNM]♂♂, PT [USNM]♀, PT [USNM]
Body (incl. sg. pl.)--87.5
Body72.063.8–65.078.5
Pronotum2.92.4–2.83.8
+
+ +......continued on the next page + +
+
+
\ No newline at end of file diff --git a/data/38/7F/30/387F3068D312FFB1FF27EDD826091FE7.xml b/data/38/7F/30/387F3068D312FFB1FF27EDD826091FE7.xml new file mode 100644 index 00000000000..976c96d33b2 --- /dev/null +++ b/data/38/7F/30/387F3068D312FFB1FF27EDD826091FE7.xml @@ -0,0 +1,233 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Cephaloplopus laetus + +n. gen. +, n. sp. + + + + +( +Figs. 80–84 +, +379 +) + + + + +HT +, ♂: +Dominican Republic +, RD-153, La Poza de Agua Nueva, El Curro, Sierra Martín García, Azua Prov., +18°18.324’N +70°57.176’W +, ~ +800 m +, +15–16.VII.2003 +, D. Perez, R. Bastardo, B. Hierro. (day/night) [USNM]. + + +PT +, ♂: +Dominican Republic +, Sierra Martín García, Azua Prov., El Curro, near caseta parques, +18°22.372'N +71°01.724'W +, +1,350 m +, +22–23/viii/2014 +, D. Perez, C. Marte, K. Rodríguez, A. Sánchez [IIBZ]. + + + + +Diagnosis: +This new species is very close to + +C. euchlorus + + +n. sp. + +but at once distinguished from this and the other known species in the genus by the shortened alae, which are hardly longer than the tegmina ( +Fig. 82 +). From + +C. euchlorus + + +n. sp. + +♂♂ (the only sex known) furthermore differ by the more robust and green legs which have only the knees brown, less distinct sub-apical tooth of the dorsal carinae of the meso- and metafemora and shape of the anal segment ( +Fig. 84 +). + + + + +Etymology: +The specific name “ + +laetus + +” (lat. = pleasant) refers to the nice and bright colouration of ♂♂. + + + + + +Description: ♂ ( +Fig. 73 +): + +The colouration is described from a photo of the live +holotype +taken at the typelocality by the third author. Of moderate size (body length 60.8–67.0 mm) and rather robust for the genus with conspicuously shortened alae (length +4.8 mm +) which are hardly longer than the tegmina; body surface glabrous. General colour pale apple green, the mesonotum, mesopleurae and lateral surfaces of the abdomen with a cream brown wash. Head creamish mid brown with the lower portions of cheeks white and the frons pale apple green ( +Fig. 81 +). Antennae ochre and becoming dark brown in the apical portion. Eyes very dark reddish brown. Pronotum brown with the lateral margins broadly green. Lower portion of metapleurae white. Spines of the mesothorax ochre, lateral lobes of abdominal tergum VII dark brown, cerci creamish mid brown. Tegmina with +anterior +margin bright yellow, then with a longitudinal brown streak, which is narrow in basal half and rather wide but weakly defined in posterior half, the innermost portion pale apple green ( +Fig. 82 +). Costal region of alae similar in colouration to tegmina but the longitudinal median stripe less distinct; anal region plain red. Legs green with the apical ¼ of all femora and tibiae mid brown; front legs with a brownish wash. Basitarsi green, the remaining tarsomeres chestnut brown. + + +Head: Globose, vertex rather convex and armed with a pair of prominent, pointed cephalad horns; the larger dextral one almost projecting by height of head capsule. Apex of the horns strongly narrowed, pointed and slightly directed towards the +anterior +( +Fig. 81 +). Two pairs of small granules are present in the posterior portion. Eyes almost circular, projecting hemispherically and their length contained less than +2x +in that of cheeks. Antennae moderately robust, very long and reaching to posterior of abdominal segment III; consisting of 54 segments. + + + +FIGURES 80–84. + +Cephaloplopus laetus + +n. gen. +, n. sp.. +80. +♂ HT, Dominican Republic, Azua Province, La Poza de Agua Nova [USNM]; +81. +Head and pronotum of ♂ HT in alteral view [USNM]; +82. +Tegmina and alae of ♂ HT [USNM]; +83. +♂ HT, apex of abdomen (dorsal view) [USNM]; +84. +♂ HT, apex of abdomen (lateral view) [USNM]. + + + +Thorax: Pronotum about equal in length but narrower than head, very slightly narrowed towards the posterior and with the lateral margins gently rounded; surface smooth except for a pair of blunt tubercles in centre of +anterior +portion ( +Fig. 81 +). Transverse median sulcus moderately distinct. Mesothorax about +3x +longer than head and pronotum combined. Mesonotum armed with four rather strong but short spines at +anterior +margin ( +Fig. 81 +), a prominent pre-medial pair of spines and a further pair of much smaller spines some 3/5 the way along dorsal surface. A row of very indistinct granules along lateral margins. Mesopleurae with a longitudinal row of minute granules, metapleurae unarmed. Mesosternum with very fine transverse sculpturing and sparsely set with a few small granules; metasternum smooth. Tegmina oval and just not reaching posterior margin of metanotum, central protuberance rather longitudinal and conspicuously displaced towards the posterior. Alae hardly longer than tegmina reaching about half way along median segment ( +Fig. 82 +). + + +Abdomen: Segments II–V roughly of equal length and about 2.8x longer than wide; very gently constricted medially with surface smooth. VI only about ¾ the length of previous. VII even shorter and with the lateral margins in posterior half expanded into a large, roundly trinagular lobe; this laterally projects by almost half the width of segment. All sternites smooth. VIII and IX just slightly shorter than VII, IX constricted medially. Anal segment shorter than IX, constricted in posterior portion and with a deep but narrow posteromedian incision ( +Fig. 84 +); on ventral surface armed with several small, black in-curving denticles. Vomer broadly triangular with the lateral margins strongly swollen; terminal hook rather short and slightly up-curving. Cerci elongate, about as long as anal segment, laterally compressed and gently in-curving. Poculum moderately convex, cymbiform, with an acute basal protuberance and carinate longitudinally ( +Fig. 83 +); posterior margin angulate. + +Legs: Profemora about equal in length mesothorax, the mesofemora slightly shorter, metafemora projecting a little over posterior margin of abdominal segment IV. Medioventral carina of profemora with two small spines in apical portion, of meso- and metafemora armed with four rather strong spines. Anteroventral carina of meso- and metafemora with two, the posteroventral carina with one sub-apical spine; both dorsal carinae very slightly expanded sub-apically. Basitarsi longer than following three tarsomeres combined. + + + +Comments: +♀♀ and eggs unknown. + + + + + +Distribution ( +Fig. 379 +): + +So far only known from the type-localites in the Sierra Martín García, Azua Province, SE-Dominican Republic: La Poza de Agua Nueva ( +800 m +) [USNM] and El Curro ( +1350 m +) [IIBZ] + + + + +Number of specimens examined: +2 + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D314FFBCFF27E84E26091EB0.xml b/data/38/7F/30/387F3068D314FFBCFF27E84E26091EB0.xml new file mode 100644 index 00000000000..0be1704890e --- /dev/null +++ b/data/38/7F/30/387F3068D314FFBCFF27E84E26091EB0.xml @@ -0,0 +1,361 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + +Cephaloplopus pulchellus + +n. gen. +, n. sp. + +(Figs. 85–99, 337, 354, 379) + + + + +HT +, ♂: +Dominican Republic +, RD-034 Boca de la +Cañada +, ~ +15 km +S Oviedo, Pedernales Prov., +4.VII.2002 +, +17°54.901’N +71°30.067’W +, B. Hierro, R. Bastardo, D. Perez [ +USNM +]. + + +PT, +♀: +Dominican Republic +, RD-034 Boca de la +Cañada +, ~ +15 km +S Oviedo, Pedernales Prov., +4.VII.2002 +, +17°54.901’N +71°30.067’W +, B. Hierro, R. Bastardo, D. Perez [ +USNM +]. + + +PT, +3 eggs +: +Dominican Republic +, RD-034 Boca de la +Cañada +, ~ +15 km +S Oviedo, Pedernales Prov., +4.VII.2002 +, +17°54.901’N +71°30.067’W +, B. Hierro, R. Bastardo, D. Perez [ +USNM +]. + + +PT, +♂: +Dominican Republic +, Parque Nacional Jaragua, Boca de la +Cañada +, +18 km +S. Oviedo, +22.–23.IX.2000 +, D. Perez, R. Bastardo, B. Hierro [ +USNM +]. + + +PT, +♂ (nymph n4): +Dominican Republic +, RD-135, ~ +7 km +Rd. to Caseta 1, Parque Nacional Sierra de Bahoruco, Independencia Prov., +18°17.711’N +71°34.335’W +, +777 m +, +VII.2003 +, D. Perez, R. Bastardo, B. Hierro (day). [ +USNM +]. + + +PT, +♂ (nymph n5): +Dominican Republic +, RD-219, Sierra Prieta, Villa Mella, Santo +Domingo +Prov., +142 m +, +18°38.925’N +69°58.303’W +, +12.IV.2004 +, D. Perez, B. Hierro, R. Bastardo. (n) [ +USNM +]. + + + + +Diagnosis: +Females differ from those of all other known species by: the very prominent, apically carinate and crenulate horns of the head ( +Figs. 87–88 +); very large, retrorse crest-like lobes of abdominal tergum II ( +Fig. 91 +) and presence of such structures on IV; very long and slender, foliaceous lateral lobes of tergum VII, which posteriorly reach half way along tergum VIII ( +Figs. 93–94 +); presence of a sub-basal lateral lobe of the subgenital plate ( +Fig. 97 +); presence of only a single prominent sub-basal lobe on the posterodorsal carina of the profemora, and very prominent lobes of the mid and hind legs. + + +The pretty ♂♂ are even more distinctive and at once differ from all other representatives of the genus by the dull green colouration and longitudinal row of 7–8 oval yellow markings along the +anterior +margin of the costal region of the alae ( +Fig. 86 +). They are furthermore well characterized by: the very long and slender cephalad horns ( +Fig. 89 +); presence of a distinct posterior pair of tubercles on the pronotum ( +Fig. 89 +); very large, slender and acutely triangular lateral lobes of abdominal tergum VII, which posteriorly reach half way along tergum VIII ( +Figs. 95–96 +) and presence of two sub-apical spines on the posteroventral carina of the meso- and metafemora. + + +The eggs can be distinguished from those of + +C. euchlorus + + +n. sp. + +, the only other eggs known from the genus, by the more distinctly sculptured capsule surface and shorter, shield-shaped micropylar plate ( +Fig. 98 +). + + + + +Etymology: +The name “ + +pulchellus + +” (lat. = beautiful) refers to the very pretty and distinctive colouration of ♂♂. + + + + + +Description: ♀ ( +Fig. 78 +). + +Rather small (body length including subgenital plate +84.5 mm +) and moderately slender for the genus, with a pair of very large crenulate horns on the head, very large foliaceous lateral lobes on abdominal tergum VII and very characteristic body and leg armature. General colour of body and legs pale creamish grey, all over furnished with whitish markings and speckles as well as dark brown mottling along the extreme margins of all body and leg appendages; abdominal segments I–IV dark brown in the unique adult ♀ at hand and most certainly caused by preservation. Head with a pair of small diverging dark brown markings on frons and a large rather obscure dark brown marking on back of vertex; above the eyes with a short and narrow dark line directed antero-posteriad. Eyes creamish mid brown, antennae greyish brown with indistinct blackish annulations. Large tubercles or spines of the thorax with brown tips and the lateral granules dark olive. Abdominal sternites II–VII broadly dark brown posteriorly. Tegmina and costal region of alae very dark brown with the latter washed with white in basal portion; anal region of alae bright red with longitudinal veins black. + + +Head: Globose, vertex strongly convex and armed with a pair of very large, apically compressed and crenulate cephalad horns, which project by more than height of head capsule (the dextral one slightly larger than the sinistral); both lateral surfaces of the horns with several spiniform tubercles ( +Figs. 87–88 +) and apex pointed medially. Posterior of vertex with several acute tubercles of variable sizes. Eyes rather small, circular and contained a little less than +2x +in length of cheeks. Antennae reaching to posterior margin of metanotum and consisting of 35 segments. Scapus dorsoventrally compressed, roundly rectangular and about +2x +longer than wide. Pedicellus cylindrical less than half the length of scapus. + + +Thorax: Pronotum slightly shorter and considerably narrower than head, 1.2x longer than wide, roughly rectangular and with the posterior margin rounded. Transverse median sulcus distinct, almost straight but not reaching lateral margins of segment. Surface with two pairs of strong but rather short spines, one +in anterior +portion and one in posterior portion ( +Fig. 88 +); otherwise with a few small, scattered granules towards the lateral margins in particular. Mesothorax about +2x +longer than head and pronotum combined. Mesonotum with a fine longitudinal median carina and with a pair of very strong but short +anterior +and pre-medial spines (the posterior pair larger, +Fig. 85 +); surface otherwise irregularly tuberculate. Meso- and metapleurae each with a longitudinal row of rounded tubercles; meso- and metasternum irregularly tuberculose. Tegmina broadly ovate and projecting slightly over posterior margin of metanotum; central protuberance very prominent, roundly conical and conspicuously displaced towards the posterior margin ( +Fig. 83 +). Alae slightly shorter than tegmina and reaching no more than ¼ the way along median segment. + + +Abdomen: Median segment roughly +2x +longer than wide and gently widened towards the posterior; a few small granules in posterior portion. Segments II–IV roughly equal in length, V–VI slightly decreasing in length and shorter than previous; IV 3.2x longer than wide. Tergites II–VI covered with a few scattered granules. II and IV each with a posterior pair of very prominent and retrorse, crenulate foliaceous lobes; these considerably larger and with the outer margin dentate on II ( +Fig. 91 +). III, V and VI merely with two very low carinae posteromedially. Tergum VII slightly shorter than VI and with the lateral margin in posterior half protruded into a large and elongate, retrorse foliaceous lobe which laterally projects by almost the bod y width and reaches as far back as the middle of tergum VIII; posterior margin irregularly dentate ( +Figs. 93–94 +). Sternites II–VI with a few scattered granules and a pair of short carinae near posterior margin; praeopercular organ represented by an elongate wart-like structure on VII ( +Fig. 337 +). Tergites VIII–X distinctly narrower than previous and roughly of uniform width; VIII ¾ the length of VII, +2x +longer than wide and constricted medially, +IX 3 +/5 the length of VIII. Anal segment shorter than IX, longitudinally carinate dorsally and with a blunt triangular tooth medio-laterally; posterior portion strongly tapered towards a narrow and medially notched apex ( +Fig. 93 +). Epiproct very small and roundly triangular. Cerci short, conical and with a rather acute apex. Subgenital plate elongate, naviculate, keeled longitudinally and projecting over abdomen by more than the combined length of tergites IX–X, apex rounded ( +Fig. 93 +). Lateral surfaces subbasally with a conspicuous rounded, lobe-like expansion ( +Fig. 97 +). + + +Legs: Profemora and mesofemora shorter than mesothorax, metafemora reaching about 1/3 along abdominal segment IV. Medioventral carina of profemora with two very small apical spines, of mesofemora armed with 4–5 and of metafemora with six rather strong spines. Anterodorsal carina of profemora with a distinct, tri-dentate apical lobe and in protibiae with a roundly triangular lobe some 1/3 off the base. Posteroventral carina of meso- and metafemora with one, the anteroventral carina with two sub-apical spines; both carinae roundly expanded in basal portion. Both dorsal carinae with a triangular lobe pre-medially and sub-apically; very large and dentate on the posterior carina but much smaller and smooth on the +anterior +carina. Posterodorsal carina of meso- and metatibiae with a small, roundly triangular lobe-like tooth some 1/3 off the base. Probasitarsus with a distinct rounded dorsal lobe and a little longer than following three tarsomeres combined ( +Fig. 92 +). Meso- and metabasitarsi slender and longer than three tarsomeres combined. + + + +♂ ( +Fig. 86 +). + +Rather small (body length +56.9–60.6 mm +) and rather slender for the genus with long alae (length +28.6–29.5 mm +) which reach to abdominal segment VI and a very characteristic colouration; body surface subglabrous. General colour of body dull green; ventral body surface, lateral surfaces of pro- and mesonotum and great parts of mesopleurae pale creamish brown with faint whitish mottling. Head green with a washed yellowish spot behind eyes, the lower +anterior +portion brown and the apices of the cephalad horns black ( +Fig. 89 +); eyes mid brown, antennae dark ochre and with a greenish wash in apical portion. Spines of the thorax with black tips. Mesopleurae with an elongate triangular green marking near posterior margin, metapleurae green. Abdominal tergites II–VI dark greyish laterally and with an obscure white posterolateral marking; lateral lobes of tergum VII dark brown. Tegmina dull green with +anterior +margin broadly blackish brown and in basal half interiorly bordered by an elongate, pale yellow marking. Costal region of alae dull green, the +anterior +margin with a broad blackish brown longitudinal stripe and furnished with a row of 7–8 oval pale yellow markings ( +Fig. 86 +). Anal region transparent pink with a greyish wash along outer margin. Legs dull green with the ventral surfaces and apex of all tibiae reddish mid brown; tarsi chestnut brown. + + +Head: General shape as in ♀♀ but with the cephalad horns very long, slender and almost cylindrical near the base; apex compressed and with one or two pointed spines; dextral horn slightly larger and projecting by more than height of head capsule ( +Fig. 89 +). Surface otherwise smooth except for two pairs of tubercles on posterior of vertex. Eyes very prominent, circular and projecting hemispherically, contained no more than 1.3x in length of cheeks. Antennae ± reaching half way along abdominal segment IV; consisting of about 52 antennomeres. + + +Thorax: Pronotum shorter and narrower than head and about 1.3x longer than wide; armature as in ♀♀ but the posterior pair of spines considerably larger than the +anterior +pair (Fig, 89). Mesothorax about 2.3x longer than head and pronotum combined. Mesonotum with a slight longitudinal median carina and armed with three pairs of short spines, the median pair largest; surface otherwise with very fine transverse sculpturing and some small granules along lateral margins. Mesopleurae granulose, metapleurae smooth. Meso- and metasternum very sparsely granulose, the mesosternum with very fine transverse sculpturing. Tegmina oval and reaching about 1/3 the along median segment, central protuberance distinct and acutely conical. Alae reaching about ¼ along abdominal segment VI. + + +Abdomen: Segments II–V of uniform length and about +3x +longer than wide; VI–VII slightly decreasing in length with VII no more than ¾ the length of II. All tergites and sternites smooth. Tergum VII with lateral margins in posterior half protruded into a very large, acutely triangular and retrorse lobe; this extending laterally by slightly more than body width ( +Figs. 95–96 +). VIII slightly shorter than VII and very gently widened in posterior portion; IX shorter than VIII and constricted towards the posterior. Anal segment with a faint longitudinal median carina, constricted at the base than distinctly expanded; the posterior margin broadly triangular with a small median indentation ( +Fig. 95 +) and on ventral surface armed with several small, black in-curving denticles. Vomer with base broadly triangular and terminal hook of moderate length and gently up-curving ( +Fig. 354 +). Cerci elongate, a little shorter than anal segment, slightly laterally compressed, tapered towards the apex and gently incurving. Poculum conically convex, cup-like, longitudinally carinate and with the posterior margin rounded ( +Figs. 96 +, +346 +). + +Legs: Profemora slightly longer, mesofemora roughly as long as mesothorax, metafemora almost reaching posterior margin of abdominal segment IV. Medioventral carina of profemora with 1–2 small sub-apical spines, of meso- and metafemora armed with four prominent, pointed spines. Both ventral carinae of meso- and metafemora with two distinct sub-apical spines, the anterodorsal carina with a triangular tooth sub-apically. Probasitarsus slightly longer, meso- and metabasitarsus about equal in length to remaining tarsomeres combined; all slender. + +Nymphs: +Even rather young nymphs are easily recognized by some of the characteristic features of this species, e.g. the very long crenulate cephalad horns or single dorsal lobe of the tibiae. As in other species of the tribe, the appendages of the body and legs are even more prominently developed than in adults and ♂ nymphs also have a pair of crenulate lobes on abdominal tergum II which are missing in the alate adult insects. The colouration is similar to that of adult ♀♀. + + + +Egg ( +Figs. 98–99 +): + +Capsule +2x +longer than wide, surface densely and unevenly tuberculate and irregularly pitted; a few enlarged tubercles roughly form some irregular ridge-like structures. A rather distinct longitudinal bulge running from the micropylar plate towards the polar-area. Polar-area merely with a very shallow indentation. Micropylar plate only about 1/3 the length of capsule, shield-shaped and about as long as wide. Colour yellowish mid brown, the outer margin of the micropylar plate dark brown. + +Measurements [mm]: Length 3.1, width 1.6, height 1.7, length of micropylar plate 1.0. + + + + +Distribution ( +Fig. 379 +): + +Hispaniola, S-Dominican Republic (Pedernales Province: Parque Nacional Jaragua; Independencia Province: Parque Nacional Sierra de Bahoruco & Santo +Domingo +Province: Sierra Prieta) [USNM]. + + + + +Number of specimens examined: +5 + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D31BFFBAFF27EB8221F31AF4.xml b/data/38/7F/30/387F3068D31BFFBAFF27EB8221F31AF4.xml new file mode 100644 index 00000000000..9d6572702af --- /dev/null +++ b/data/38/7F/30/387F3068D31BFFBAFF27EB8221F31AF4.xml @@ -0,0 +1,1089 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +5.4 +. Genus + +Diapherodes +Gray, 1835 + + + + + + + +Type-species: + +Mantis gigantea +Gmélin, 1789 +: 2055 + +, by subsequent designation of +Kirby, 1904a +: 362. + + + + + +Diapherodes +Gray, 1835 +: 33 + +(in part). +Burmeister, 1838 +: 560, 573 (in part). +Westwood, 1859 +: 84 (in part). Saussure, 1872: 185 (in part). +Stål, 1875 +: 31. + + +Bolivar, 1888 +: 140 (in part). +Kirby, 1904a +: 362 (in part). +Redtenbacher, 1908 +: 434 (in part). Rehn, 1909: 200. + +Wolcott, 1922: 23. + +Wolcott, 1936 +: 35. + + +Rehn & Hebard, 1938 +: 53, pl. 4: 22 (♀). +Wolcott, 1948 +: 50. + + +Wolcott, 1951 +: 50. + + +Moxey, 1972 +: 85 (in litt.; in part). + + +Langlois & Lelong, 1997 +: 43, fig. 20 (♂, ♀). + + +Brock, 1998c +: 33. + +Langlois, Lelong, Rastel, Polidori & Dorel, 2000: 46, fig. 19-g (♂, ♀) & photos 10–12 (egg). + +Lelong, Langlois, Rastel & Dorel, 2003 +: 48, fig. 19a–g (♂, ♀) & photos 11–13 (egg). + + +Lelong & Langlois, 2005 +: 264. + + +Otte & Brock, 2005 +: 120 (in part). + + +Langlois, +Lelong & Rastel, 2006 +: 42, figs. 19 a–g (♂, ♀, nymph), photos 5–6 (♀) & 27–29 (egg). + +Aplopus +, +Redtenbacher, 1908 +: 429 + +(in part). + + +Rehn, 1904 +: 68 (in part). + +Rehn, 1909: 200. + +Wetmore, 1916 +: 58. + + +Wolcott, 1923 +: 23. + + +Wolcott, 1936 +: 35. + + +Wolcott, 1948 +: 50. + + +Wolcott, 1951 +: 50. + + +Otte & +Brock, 2003 +: 301 (in part). + + + +Aplopus + +(?), +Rehn & Hebard, 1938 +: 52. + + + + +<emphasis id="82A25D6CD31AFFBFFF27EC89257C1FBB" box="[151,276,734,756]" italics="true" pageId="59" pageNumber="60">Cyphocrana</emphasis> +, St + +. +Fargeau & Audinet-Serville +, +1825 +: +445 +. + + +Audinet-Serville, 1831: 61. + + +Haplopus +, Westwood, 1859: 85 + +(in part). + +Kirby, 1904a: 363 (in part). + + +Mantis +, Drury, 1773: 88 + +, 89, pl. 44: 1 & 50 (in part). + +Fabricius, 1775: 274. +Fabricius, 1787: 227. + +Gmélin, 1789: +2054-2055 +. + +Olivier, 1792: 634. +Fabricius, 1793: 13. + + +Phasma +, Fabricius, 1798: 187 + +, 188. + +St. Fargeau & Audinet-Serville, 1825: 101. + +Westwood, 1859: 34, pl. 22: 7, 7a, 7b (♀). + +Phasma (Diapherodes) +, de Haan, 1842: 109 + +. [ +Not: + +Diapherodes +, Saussure, 1872: 183 + +. à + +Venupherodes + + +n. gen. + +] + + + + +Description: ♀♀, ♂♂. +Medium-sized to very large (body lengths: ♀♀ 92.0–197.0 mm, ♂♂ 60.0–126.0 mm) and moderately slender to very robust Haplopodini. ♀♀ in particular, often broad to very broad and massive insects with the body distinctly oval in cross-section and the thorax and abdomen conspicuously broadened; brachypterous. ♂♂ moderately slender, body cylindrical or sub-cylindrical in cross-section, with scale-like tegmina and well developed alae. Body surface of ♀♀ ± shiny, colouration usually plain bright green (rarely brown or with brown markings), ♂♂ brown or green. Head globose, indistinctly longer than wide. Vertex roundly convex, tuberculose and armed with a pair of ± prominent tubercles or blunt spines. Antennae with all antennomeres moderately thickened and longer than head and thorax combined. Scapus dorsoventrally flattened, longer than pedicellus. Pronotum tuberculose, with or without a ± prominent pair of blunt spines or tubercles +in anterior +half. Mesothorax at best slightly more than +2x +the length of head and pronotum combined, in ♂♂ slender and roughly parallel sided, in ♀♀ ± strongly widened towards the posterior and constricted anteriorly. Mesonotum anteriorly armed with 2–6 distinct spiniform tubercles or spines; surface otherwise smooth, sparsely granulose or tuberculose. Meso- and metapleurae of ♀♀ ± strongly expanded and laterally projecting over mesonotum; armed with a longitudinal marginal row of ± prominent tubercles, teeth or spines. Meso- and metasternum either smooth, both granulose, or only the mesosternum with a few scattered granules. ♀♀ with scale-like tegmina which at best slightly project over posterior margin of metanotum. Alae at best slightly longer than the tegmina, but usually much shorter and may be vestigial. Tegmina of ♂♂ oval, longer than metanotum and with a ± distinct conical central hump. Alae at least reaching to posterior margin of abdominal tergum V. Anal region of alae transparent pink or violet (♀♀), plain transparent white, pink or orange (♂♂). Abdomen distinctly longer than head and complete thorax combined; unarmed in ♂♂, tergites sometimes finely multi-carinate in ♀♀. Abdomen of ♀♀ ± broadened and swollen basally or sub-basally, with segments II and/or III the broadest, then gradually narrowing towards the apex. Abdomen of ♂♂ slender and cylindrical with the terminal three segments slightly broader than previous. In ♀♀ segments II–IV transverse to quadrate, V to VII slightly longer than wide; in ♂♂ II–VII parallelsided and 1.5–2.5x longer than wide. Tergum VII of ♀♀ with lateral margins ± rounded and/or expanded, or with a triangular posterolateral lobe; in ♂♂ parallel-sided or with a small lobe posterolaterally. Praeopercular organ of ♀♀ indistinct; formed by a single posteromedian granule or wart-like tubercle on sternum VII. Cerci very small, oval in cross-section and tapered towards the apex; slightly in-curving in ♂♂, often hidden underneath anal segment in ♀♀. Epiproct very small and mostly hidden underneath anal segment. Vomer short and broad; roughly triangular. Subgenital plate of ♀♀ keeled, narrowed towards a ± pointed apex and extending considerably beyond apex of abdomen. Poculum of ♂♂ strongly convex and cup-like. Legs of moderate length and rather broad. Profemora at best about as long as mesothorax, hind legs not reaching to apex of abdomen. Medioventral carina of femora armed with a longitudinal row of spines (often indistinct on profemora). Both dorsal carinae of meso- and metafemora occasionally with a sub-apical lobe, the ventral carinae each with 1–2 distinct and pointed sub-apical spines. Some carinae of mid and hind legs may be ± elevated and ledge-like in ♀♀ of certain species. Basitarsi short, at best slightly longer than following two tarsomeres combined. + + +Eggs: +Medium-sized to large (capsule length +3.7–5.6 mm +), ovoid and cylindrical in cross-section; capsule 1.5–2.0x longer than wide. Polar-area ± impressed in lateral aspect. Capsule surface strongly coriaceous and covered with irregular raised tubercles and ridges to a variable degree. Micropylar plate generally drop or heartshaped, narrowed towards +anterior +end and broadened basally, at least 1/3 the length of capsule; central portion sculptured like capsule. Posterior end of micropylar plate with a wide triangular gap. Median line distinct. Operculum flat to slightly convex, circular and in the centre structured like capsule; no conspicuous central capitulum. Colouration irregularly grey or brown. + + + + +Differentiation: +Closely related to the Cuban + +Venupherodes + + +n. gen. + +and + +Haplopus +Burmeister, 1838 + +. Slender representatives of the + +jamaicensis + +-group in particular resemble stockier representatives of + +Haplopus + +. + + +However, + +Diapherodes + +is absent in +Cuba +and easily distinguished from + +Venupherodes + + +n. gen. + +by: the larger size (♀♀ in particular); unicolourous head of ♂♂; elevated and prominently armed mesopleurae which laterally project over the mesonotum; mesothorax which is gradually broadened towards the posterior; lack of a longitudinal median keel of the mesonotum; presence of tegmina and alae; basally or sub-basally broadened abdomen; simple praeopercular organ and longer subgenital plate of ♀♀. The eggs at once differ by the less strongly sculptures capsule surface and longer, elongate micropylar plate (→ +Table 33 +). + + +From + +Haplopus + +it differs by: the broader and more robust body (♀♀ in particular); relatively shorter mesothorax (at best a little more than +2x +the length of head and pronotum combined); shorter basitarsi and plain anal region of the alae of both sexes; oval body cross-section and more decidedly broadened meso- and metathorax of ♀♀, as well as the smaller and much more slender cerci ♂♂. Furthermore, ♀♀ are mostly plain bright green, whereas ♀♀ of + +Haplopus + +are brown or grey. The eggs clearly differ from those of + +Haplopus + +by having the capsule surface much more prominently sculptured and lacking a distinct hat- or knob-like central capitulum. + + + + +Comments: +The classification of + +Diapherodes + +has varied through the years, but in the way treated by Redtenbacher (1908: 434) the genus was paraphyletic and as interpreted by Moxey (1972: 85 ff., in litt.) included five generic units. Several features of the insects and eggs indicate two species-groups within the genus, here recognized as the + +gigantea + +-group and + +jamaicensis + +-group. These two groups are geographically rather well separated, members of the + +gigantea + +-group being restricted to the Lesser Antilles, and the three known species of the + +jamaicensis + +-group occuring only on the Greater Antillean islands of +Jamaica +and +Puerto Rico +(→ 6.). + + +The systematic level of sub-genera was considered for these two groups of species in + +Diapherodes + +, but due to the lack of satisfying distinctive features in the eggs in particular, interpreting these solely as species-groups appears more appreciable. For a better understanding of the present arrangement a detailed comparison of these two species-groups here proposed appears warranted and is presented below (→ +Table 10 +). + + + + + +Distribution ( +Fig. 375 +): + +Lesser Antilles ( +Guadeloupe +, +Dominica +, +Martinique +, +Saint Lucia +, +Grenada +, & +Saint Vincent +→ + +gigantea + +-group, +Fig. 381 +) and Greater Antilles ( +Puerto Rico +& +Jamaica +→ + +jamaicensis + +-group). + + + + + + + +Species & subspecies included: + + + + + + +I. + +Gigantea + +-group + + + + +1. + +Diapherodes angulata +(Fabricius, 1793: 13) + +[ + +Mantis + +]. +rev. stat. + + += + +Haplopus grayi +Kaup, 1871: 36 + +. +n. syn. +[Distribution: +Guadeloupe +] + + +2. + +Diapherodes dominicae +(Rehn & Hebard, 1938: 53) + +. +n. comb. +[Distribution: +Dominica +] + + +3. + +Diapherodes gigantea gigantea +(Gmélin, 1789: 2055) + +[ + +Mantis + +]. = + +Mantis gigas +Drury, 1773: 89 + +, pl. 50 (♀). = + +Cyphocrana cornuta +St. Fargeau & Audinet-Serville, 1825: 445 + +. [Distribution: +Saint Vincent +& +Grenada +] + + +4. + +Diapherodes gigantea saintluciae + + +n. ssp. + + + +[Distribution: +Saint Lucia +] + + +5. + +Diapherodes martinicensis +Lelong & Langlois, 2005: 264 + +. [Distribution: +Martinique +] + + + + +II. + +Jamaicensis + +-group + + + + +6. + +Diapherodes achalus +(Rehn, 1904: 68) + +[ + +Aplopus + +]. +n. comb. += + +Diapherodes longiscapha +Redtenbacher, 1908: 435 + +. +n. syn. +[Distribution: +Puerto Rico +] + + +7. + +Diapherodes jamaicensis + +(Drury, 1773: 88, pl. 44: 1 (♂)) [ + +Mantis + +]. = + +Mantis bispinosa +Fabricius, 1775: 274 + +. + + += + +Haplopus christopheri +Westwood, 1859: 84 + +, pl. 33: 4, 4a (♀). +n. syn. += + +Diapherodes glabricollis +Gray, 1835: 33 + +. +n. syn. += + +Haplopus murinus +Redtenbacher, 1908: 429 + +. +n. syn. += + +Dipaherodes pulverulentus +Gray, 1835: 34 + +. +n. syn. +[Distribution: +Jamaica +] + + +8. + +Diapherodes laevicollis +Redtenbacher, 1908: 434 + +. [Distribution: +Jamaica +] + + + + +TABLE 10. +Comparison of the +gigantea- +group and +jamaicensis- +group of + +Diapherodes +Gray, 1835 + +. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+ +gigantea +-group + + + +jamaicensis +-group + +
+Body length (♂♂) +64.0–126.0 mm61.5–76.5 mm
+Body length (♀♀) +92.0–197.0 mm104.0–164.5 mm
+Pronotum + +With a pair of prominent +anterior +spines + +No +anterior +spines +
+Mesonotum (♂♂) +Granulose or tuberculoseSmooth
+Mesonotum (♀♀) +No median carina; surface armed with several blunt tubercles or spinesWith an indistinct longitudinal median carina; surface ± granulose or tuberculose
+Meso- and metapleurae (♂♂) +Granulose or tuberculoseSmooth
+Meso- and metapleurae (♀♀) +Strongly deflexed and armed with a marginal row of prominent teeth or spinesGently expanded and with a marginal row of granules or acute tubercles
+Meso- and metasternum (♂♂) +GranuloseSmooth
+Metasternum (♀♀) +Granulose or tuberculoseSmooth
+Alae (♀♀) +Vestigial; <half the length of tegmina± as long as tegmina
+Abdominal tergum VII (♀♀) +Lateral margins gently roundedWith a small posterolateral lobe or distinctly deflexed laterally
+Epiproct (♀♀) +Very small and mostly fully concealed by anal segmentLarge triangular to shield-shaped and projecting over anal segment
+Egg (capsule length) +4.1–5.6 mm3.5–3.8 mm
+Egg (micropylar plate) +Elongate; ± ½ as long as capsuleAbout as long as wide; ± 1/3 the length of capsule
+Distribution +Lesser Antilles (Fig. 381)Greater Antilles (Puerto Rico & Jamaica)
+
+ + + + + +Keys to the species and subspecies of + +Diapherodes + + + + + +♀♀* + + + + + +1. Meso- and metapleurae strongly expanded and with a prominent marginal row of teeth or spines; pronotum with a distinct pair of +anterior +spines; alae vestigial, <½ the length of tegmina; Lesser Antilles........................ 2. ( + +gigantea + +-group) + + + + +- Meso- and metapleurae tuberculose; no +anterior +spines on pronotum; alae ± as long as tegmina; Greater Antilles ( +Jamaica +& +Puerto Rico +)......................................................................... 6. ( + +jamaicensis + +-group) + + + + + + +2. Body length> +11 cm +; mesonotum> 1.5x longer than head and pronotum combined;> 50 antennomeres................. 3 + + + + +- Body length < +10 cm +; mesonotum only 1.3x longer than head and pronotum combined ( +Fig. 144 +); 37 antennomeres; +Martinique +( +Fig. 381 +).............................................................................. + +martinicensis + + + + + + + +3. Body length < +15 cm +; mesonotum with numerous spiniform tubercles or spines; carinae of mid and hind legs not conspicuously expanded and dorsal carinae not dentate............................................................... 4 + + + + +- Very large, body length> +15 cm +( +Figs. 120–122 +); mesonotum unarmed or at best with six enlarged spines +in anterior +portion; mid and hind legs with carinae ± strongly expanded and acutely dentate ( +Fig. 132 +); +Saint Vincent +& +Grenada +( +Fig. 381 +)........................................................................................... + +gigantea gigantea + + + + + + + +4. Small, body length < +14 cm +; head bi-tuberculate............................................................. 5 + + + + +- Large, body length> +14 cm +, head prominently bi-cornute ( +Fig. 107 +); +Guadeloupe +( +Fig. 381 +).................... + +angulata + + + + + + + +5. Spines of meso- and metapleurae considerably longer than width of base, acute; tegmina large and overlapping ( +Figs. 136–137 +); +Saint Lucia +( +Fig. 381 +).................................................... + +gigantea saintluciae + + +n. ssp. + + + + + +- Spines of meso- and metapleurae small and blunt ( +Figs. 109–110 +); tegmina small and leaving a distinct gap between each other ( +Figs. 109–110 +); +Dominica +( +Fig. 381 +)............................................................... + +dominicae + + + + + + +6. Slender insects; mesothorax slightly widened towards the posterior,> 2.5x longer than head and pronotum combined; abdominal tergum VII gently broadened and indistinctly broader than VI............................................... 7 + + + +- Very massive insects ( +Figs. 183–184 +); mesothorax strongly broadened towards the posterior, only about 2.1x longer than head and pronotum combined; abdominal tergum VII prominently laterally expanded; almost +2x +broader than VI ( +Fig. 186 +); +Jamaica +...................................................................................... + +laevicollis + + + + + + +7. Slender insects ( +Figs. 167–170 +); head globose and distinctly bi-cornute ( +Fig. 173–174 +); mesonotum granulose and with 2–4 +anterior +spines, not keeled; abdomen slender; +Jamaica +................................................. + +jamaicensis + + + +- Broader insects ( +Fig. 157 +); head longer than wide and faintly bi-tuberculate ( +Fig. 159 +); mesonotum smooth and with a longitudinal median carina; abdomen distinctly broadened sub-basally; +Puerto Rico +................................. + +achalus + + + +* body lengths given are including the subgenital plate +♂♂ + + +1. Mesonotum irregularly granulose, tuberculose or spinose; metasternum and pleurae granulose; Lesser Antilles ( +Fig. 381 +).......................................................................................... 2 ( + +gigantea + +-group) - Mesonotum unarmed (may have 2–8 +anterior +spines), metasternum and pleurae unarmed; Greater Antilles ( +Jamaica +& +Puerto Rico +).............................................................................. 6 ( + +jamaicensis + +-group) 2. Mesonotum tuberculose or spinose; colouration of body, tegmina and costal region of alae brown...................... 3 Mesonotum sparsely granulose; body, tegmina and costal region of alae green ( +Figs. 101–102 +); +Guadeloupe +( +Fig. 381 +).................................................................................................... + +angulata + +3. Head distinctly bi-cornute; +anterior +margin of tegmina white or pale yellowish..................................... 4 - Cephalad pair of tubercles obsolete ( +Fig. 113 +); +anterior +margin of tegmina bright yellow and green with a dark green stripe interiorly ( +Fig. 117 +); +Dominica +( +Fig. 381 +)........................................................... + +dominicae + +4. Mesothorax elongate> 1.7x longer than head and pronotum combined; alae at best reaching to posterior margin of abdominal tergum VI; ventral portion of tegmina without distinct colouration............................................... 5 - Mesothorax short, only 1.5x longer than head and pronotum combined; alae reaching to posterior margin of abdominal tergum VII ( +Figs. 146–147 +); central portion of tegmina bright purple; +Martinique +( +Fig. 381 +)...................... + +martinicensis + +5. Body length> +9 cm +; tubercles of pro- and mesonotum dull green ( +Fig. 125 +); alae at best reaching half way along abdominal tergum VI; +Saint Vincent +& +Grenada +( +Fig. 381 +)................................................ + +gigantea gigantea + +- Body length < +9 cm +; tubercles of pro- and mesonotum black; alae reaching to posterior margin of abdominal tergum VI; +Saint Lucia +( +Fig. 381 +).................................................................. + +gigantea saintluciae + + +n. ssp. + +6. Mesonotum with 2–8 distinct paired +anterior +spines; alae at best reaching to abdominal tergum VI; tegmina plain green; +Jamaica +............................................................................................. 7 - Mesonotum unarmed, at most with some minute granules; alae projecting over tergum VII; tegmina with a brown longitudinal median stripe ( +Fig. 158 +); +Puerto Rico +................................................................ + +achalus + +7. Slender; mesonotum +2x +longer than head and pronotum combined; alae reaching to posterior of abdominal tergum VI ( +Figs. 171–172 +); scapus and pedicellus greenish or brown ( +Fig. 175 +).......................................... + +jamaicensis + +- +More robust; mesonotum 1.8x longer than head and pronotum combined; alae reaching to posterior of abdominal tergum VII ( +Fig. 185 +); scapus and pedicellus black............................................................. + +laevicollis + + + + +
+
\ No newline at end of file diff --git a/data/38/7F/30/387F3068D31EFFC7FF27ECA821641865.xml b/data/38/7F/30/387F3068D31EFFC7FF27ECA821641865.xml new file mode 100644 index 00000000000..22944d844f5 --- /dev/null +++ b/data/38/7F/30/387F3068D31EFFC7FF27ECA821641865.xml @@ -0,0 +1,700 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Diapherodes angulata +(Fabricius, 1793) + +rev. stat. + + + + +( +Figs. 100–108 +, +346 +, +365 +, +381 +) + + + + + +Mantis angulata +Fabricius, 1793: 13 + +. +Type +(s), ♀ (♀): +Insula +Guadeloupe +Dom. +De +Badier (not traced—presumed lost). [Unnecessary replacement name for + +Mantis gigas +Drury, 1773 + +]. +NT ( +by present designation), ♀: +Guadeloupe +Le Moult [MNCN]. + + + +Phasma angulata +, Fabricius, 1798: 187 + +. + + + +Phasma angulatum +, +Lichtenstein +, 1802: 11 + +. + + + +Cyphocrana angulata +, Audinet-Serville, 1831: 61 + +. + + + +Diapherodes angulata +, Burmeister, 1838: 547 + +. + +Rehn, 1903: 136. + + +Brock, 1998c: 33. + + + + +Haplopus grayi +Kaup, 1871: 36 + +, pl. 2: 1 (♀) & 20, pl. 1: 20 (eggs). +HT +, ♀: + +Haplopus Grayi +Kaup Mol. + +v. Rosenberg, +Holotypus +[HLDH]. +n. syn. + + +Moxey, 1971: 99 (in litt.). [Listed as a synonym of + +Diapherodes gigas +(Drury, 1773) + +— +in error +] + + + +Diapherodes grayi +, Kirby, 1904a: 363 + +. + +Otte & Brock, 2003: 305. + + +Diapherodes gigantea +, Redtenbacher, 1908: 434 + +(in part). + +Moxey, 1972: 99 (in litt.; in part). + + +Diapherodes gigas +, Moxey, 1971: 98 + +(in litt.; in part—only specimens from +Guadeloupe +). Langlois & Lelong, 1997: 43, figs. 20a (♀) & 20 b (♂). + +Lelong & Langlois, 2001: 242, figs. 1 (♀), 2 (♂). + + + +[ +Not: + +Phasma angulata +Stoll, 1813: 61 + +, pl. 21: 77 (♀), = + +Haplopus micropterus + +(St. Fargeau & Audinet-Serville, 1825: 445] + + + + +Further material [14 ♀♀, 21 ♂♂, 6 nymphs, eggs]: + + +GUADELOUPE +: + + +5 ♀♀, 5 ♂♂, 2 ♂♂ (nymphs): +Guadeloupe +Le Moult [ +MNCN +]; 1 ♀, 2 ♂♂: +Guadeloupe +Trois Rivières; D.Vitrac Dedit.; Collection A. Finot, + +Diapherodes gigas +, Drury + +[ +MNHN +, coll. Finot, box no. 294]; 1 ♀: +Guadeloupe +Trois Rivières; D.Vitrac Dedit.; Collection A. Finot, + +Diapherodes gigas +, Drury + +[ +MNHN +]; Eggs (ex abdomen): + +Diapherodes gigas +Drury, Trois Rivières + +, +Guadeloupe +, 69.321 [ +MNHN +]; 1 ♀, +1 ♂ +, +1 ♂ +(penultimate instar), 2 ♀♀ n5: +Guadeloupe +, Gourbeyre 1896 + +Diapherodes gigas +Drury + +[ +MNHN +]; +1 ♂ +: Vernou, +15–30-VI- +19771; Museum Paris +Guadeloupe +, A. Villiers [ +MNHN +]; 5 ♂♂: M. Delfosse Elevage ♂ 1993; + +Diapherodes gigantea gigantea +(Gmélin, 1789) + +, E. Delfosse Dét. +23/02/03 +[ +MNHN +]; 1 ♀: M. Delfosse, +Guadeloupe +♀ Elevage 1994; + +Diapherodes gigantea gigantea + +[ +MNHN +]; +1 ♂ +: M. Delfosse, Basse-Terre, +Guadeloupe +90; + +Diapherodes gigantea gigantea + +04/05 [ +MNHN +]; 1 ♀: M. Delfosse, Elevage, +Guadeloupe +, 1993; + +Diapherodes gigantea gigantea +(Gmélin, 1789) E. Delfosse Dét. + +04/05 [ +MNHN +]; 2 ♂♂: M. Delfosse +Guadeloupe +, 6/1993; Elevage, + +Diapherodes gigantea + +[ +MNHN +]; +1 ♂ +: M. Delfosse, +Guadeloupe +, 07/1993 [ +MNHN +]; 2 ♂♂: M. Delfosse +Guadeloupe +♂ 04/1993; Elevage, + +Diapherodes gigantea + +[ +MHNH +]; 1 ♀: +Guadeloupe +, Antilles ♀; + +Diapherodes gigas +Drury + +[ +MHNG +]; 1 ♀: Antilles; + +Diapherodes gigas +Drury + +[ +MHNG +]; 1 ♀: 3/33 +Guadeloupe +, Mr. H. d. Sauss.; + +Diapherodes gigas +Drury + +[ +MHNG +]; 1 ♀ (nymph): Larve, +Guadeloupe +, Mr. H. d. Sauss; + +Diapherodes gigas +Drury + +[ +MHNG +]. + + +NO +DATA +: + + +1 ♀: no data [ +NHMUK +]; +1 ♂ +: no data [ +MNHN +]. + + + + +FIGURES 100–102. + +Diapherodes angulata +(Fabricius, 1793) + +. +100. +♀: Guadeloupe, Trois Rivères [MNHN]; +101. +♂: Guadeloupe [MNHN]; +102. +♂: Guadeloupe [MNHN]. + + + + +Diagnosis: +Distinguished from the type-species + +D. gigantea gigantea +(Gmélin, 1789) + +by: the smaller size and prominently bi-spinose vertex of both sexes; more numerous but smaller spiniform tubercles of the mesonotum; shorter and more numerous spines of the marginal row of the meso- and metapleurae; more slender legs and much less prominently dentate, not considerably expanded carinae of the mid and hind legs of ♀♀ ( +Fig. 106 +). From + +D. dominicae +(Rehn & Hebard, 1938) + +♀♀ differ by: the larger size; more robust legs; much more prominent cephalad pair of spines ( +Fig. 107 +); less numerous but more pronounced tubercles of the mesonotum; larger +anterior +pair of spines on the pronotum; larger and more pointed spines of the meso- and metapleurae ( +Fig. 100 +) and larger, broader tegmina which overlap interiorly ( +Fig. 100 +). ♂♂ are at once distinguished from all other representatives of the + +gigantea + +species-group by the green body, tegmina and costal region of the alae and very sparsely granulose mesonotum ( +Figs. 101–102 +). + + + + +FIGURES 103–108. + +Diapherodes angulata +(Fabricius, 1793) + +. +103. +♀ NT, apex of abdomen (lateral view) [MNCN]; +104. +♀ NT, apex of abdomen (dorsal view) [MNCN]; +105. +Apex of ♂ abdomen (lateral view) [MNHN]; +106. +Right hind leg of ♀ NT (posterolateral view) [MNHN]; +107. +Head and pronotum of ♀ NT [MNHN]; +108. +Head and pronotum of ♂ [MNHN]. + + + + + +Description: ♀ ( +Fig. 100 +). + +Medium-sized to large (body length including subgenital plate 141.0– +162.5 mm +) and moderately broad for the genus. General colouration usually plain pale to mid green, the ventral body surface with a whitish wash; occasionally olive or pale to mid brown specimens may occur. Ventral surface of meso- and metapleurae white, spines of the longitudinal marginal row dull orange to very dark red. Dorsal spines of the head and thorax orange with ochre bases. Tegmina and alae of same colouration as body. Antennae pale brown, the two basal segments greenish. Tarsi greenish pale to mid brown. Eyes dull orange to reddish mid brown. + + +Head: Globose, vertex strongly convex and armed with two prominent, blunt to fairly acute spines; a few small granules are present in the posterior portion ( +Fig. 107 +). Eyes circular, convex and of moderate size; their length contained about 2.3x in that of cheeks. Between the bases of the antennae with two rather distinct, oval impressions. Antennae longer than fore legs and laid back, projecting over posterior margin of median segment; with more than 60 segments. Scapus dorsoventrally flattened, +2x +longer than wide and gently narrowed towards the base. Pedicellus cylindrical, slightly constricted towards the apex and about half as long as scapus. + + +Thorax: Pronotum slightly shorter and narrower than the head; indistinctly longer than wide and gently widened towards the posterior. In front of the very prominent and well defined, slightly curved transverse median sulcus armed with a large pair of rather long, blunt spines; posterior half with a more or less decided pair of tubercles close to posterior margin and one small tubercle at each posterolateral angle ( +Fig. 107 +). Mesothorax 1.6–1.7x longer than head and pronotum combined, and decidedly constricted anteriorly. Mesonotum dorsally armed with two pairs of spiniform tubercles close to +anterior +margin ( +Fig. 107 +) and two or three further pairs of slightly enlarged tubercles in the +anterior +half of the dorsal surface; otherwise irregularly set with a few small tubercles. Along lateral margins with a longitudinal row of small, rounded granules. Metanotum unarmed, about 2/ 5 the length of mesonotum and about as long as wide. Spines of the meso- and metapleurae very distinct and acute; the longest being about +2x +as long as its basal width. Mesopleurae with 17–22, metapleurae with 13–17 spines. Meso- and metasternum each with a variable number of pointed tubercles, which are more decided and larger on the metasternum. Tegmina rather large for the genus and usually slightly projecting over posterior of metanotum (length 11.9–13.0 mm) with posterior margin roundly angulate; overlapping or leaving a small space (up to +3 mm +) inbetween them. Alae very small, projecting underneath tegmina by only about 0.5–2.0 mm. + + +Abdomen: Median segment slightly longer than metanotum and trapezoidal, being gently narrowed towards the +anterior +. Segments II–V roughly of equal length, VI and VII slightly shorter. II–IV about 1.6–1.7x wider than long, VI about as long as wide. VII narrower and slightly longer than VI, parallel-sided. Praeopercular organ formed by an elongate, longitudinal swelling near posterior margin of sternum VII ( +Fig. 346 +). Tergum VIII slightly about 2/3 the length and narrower than VII, decidedly more convex than previous and gently widened towards the posterior. IX about half as long as VIII and slightly wider than long. Anal segment longer than IX, gently narrowed towards the posterior and with a faint longitudinal median keel dorsally ( +Fig. 104 +). Posterior margin broadly rounded and with a very shallow median indentation, the lateral margins with a concave excavation at bases of cerci. Epiproct very small and hidden under anal segment. Subgenital plate long and gradually narrowed towards a pointed tip; projecting over apex of abdomen by at least the combined length of tergites IX and X ( +Figs. 103–104 +). + + +Legs: All of moderate length, profemora about as long as mesothorax and metatibiae reaching about halfway along abdominal tergum VIII. All carinae densely and sharply but very minutely granulate or denticulate (more decided on mid and hind legs). Mid and hind legs decidedly carinate ( +Fig. 106 +). Medioventral carina of meso- and metafemora blunt but low and with 4–6 stout spines which decrease in size towards the base of femur. Posteroventral carina with one, anteroventral carina with two rather small pointed sub-apical spines. Anterodorsal carina of meso- and metatibiae very weakly rounded apically. Basitarsus about 1.3x longer than second tarsomere. + + + +♂ ( +Figs. 101–102 +). + +Medium-sized to large (body length 93.5–110.0 mm) and stocky for the genus, with long alae (53.0–56.0 mm) and a moderately, dorsally sparingly granulose mesothorax. General colouration pale yellowish green to mid green, the tegminal and costal region of the alae with distinctly darker longitudinal veins. Ventral thoracal segments and abdominal sternum II dull green, abdominal sternites III–VII whitish. Vent ral surfaces of meso- and metapleurae white. Largest tubercles of the head and dorsal surface of the thorax tipped with dull orange. Tegmina and costal region of same colouration as body, the tegmina with a broad longitudinal and very pale creamish green stripe along the +anterior +margin which is continued in the basal quarter of the alae. Bases of alae pale red, anal region hyaline. Antennae pale to mid brown and becoming gradually darkler brown towards the apex, two basal segments greenish. Eyes dark orange to reddish brown. + + +Head: Generally as in ♀♀. Vertex strongly convex and smooth except for two blunt but well decided, conical tubercles; posterior portion usually with two small granules ( +Fig. 108 +). Eyes large, cylindrical and projecting hemispherically; their length contained about +2x +in that of cheeks. Antennae reaching halfway along abdominal tergum III, otherwise structured like in ♀♀. About 70 antennomeres. + + +Thorax: Pronotum shorter and slightly narrower than head, about as long as wide with the +anterior +margin slightly widened. Otherwise generally as in ♀♀ but armature less distinct ( +Fig. 108 +). Mesothorax rather elongate, about +2x +longer than head and pronotum combined; mesonotum almost +6x +longer than wide. +Anterior +of mesonotum with a well decided pair of blunt tubercles, dorsal surface otherwise irregularly set with a few low tubercles and granules; a longitudinal row of small granules along lateral margins. Meso- and metapleurae each with a longitudinal row of minute granules. Meso- and metasternum sparsely granulose. Alae reaching halfway along tergum VI. + + +Abdomen: Tergum VII with posterolateral angles very gently expanded and rounded. Tergum +VIII 2 +/3 of VII and gradually widened towards the posterior, broadest segment. IX ¾ the length of VIII and very weakly narrowed towards the posterior. Posterior half of tergum VII, as well as VIII and IX with two parallel, longitudinal carinae dorsomedially. Anal segment with a very faint longitudinal median keel, the posterior portion abruptly narrowed and with a broadly triangular median indentation. Sternum VIII with an acute longitudinal median carina. Vomer triangular with basal portion strongly broadened and almost equal to overall length, terminal hook short and slender ( +Fig. 365 +). Poculum granulose, convex and cup-like ( +Fig. 105 +) with the posterior margin broadly triangular ( +Fig. 365 +); indistinctly projecting over posterior margin of tergum IX. + +Legs: All of moderate length for the genus, profemora slightly longer than mesonotum, metatibiae almost reaching posterior margin of abdominal tergum VII. All carinae densely but very minutely granulate to denticulate. Posteroventral carina of meso- and metafemora with one, anteroventral carina with two, slender and pointed subapical spines. Medioventral carina broad and flat, armed with 5–6 short but strong spines which decrease in size towards the base of femur. Tarsi rather stout, slightly less than half the length of corresponding tibia. Basitarsi about 1.3x longer than second tarsomere. + + + +Comments: +This species was first described by Fabricius (1793: 13) who stated the +type +locality to be “ +Insula +Guadeloupe +”. The original ♀ +type +specimen(s) is not traced in ZMUC nor in any other likely collection and hence believed lost (Brock, 1998c: 33). Fabricius (1793) based his description on a specimen(s) from +Guadeloupe +and introduced + +Mantis angulata + +as a replacement name for + +Mantis gigas +Drury, 1773 + +, which had however already been replaced by + +Mantis gigantea +Gmélin, 1798 + +. The name of Fabricius is therefore an unnecessary replacement name and a junior objective homonym of + +Mantis gigantea +Gmélin. + + +Diapherodes gigantea +(Gmélin, 1789) + +is endemic to +Grenada +and +Saint Vincent +and detailed examination of several specimens, including ♂♂, from +Guadeloupe +in MNCN and MNHN has shown these to be a distinct species. As the +type +specimen(s) on which Fabricius (1793: 13) based his description of + +Mantis angulata + +were from +Guadeloupe +and represent a distinct species, + +Mantis angulata +Fabricius + +is not a synonym of + +Mantis gigantea + +and becomes an available name ( +rev. stat. +). Therefore the specific name of Fabricius (1793) is here re-introduced and used for the species from +Guadeloupe +. As the original type-specimen(s) is lost, an almost perfect ♀ in MNCN from a series of specimens with the data “ +Guadeloupe +Le Moult” is here selected as the +neotype +of + +Mantis angulata +Fabricius, +1793 + +in order to ensure stability of the name. Further specimens from the same source are in MNHN. + + +Kaup (1871: 36, pl. 2: 1) described and figured + +Haplopus grayi + +from a ♀ wrongly labelled “ +Molukken +”, but there can however be no doubt his specimen originated from the Lesser Antilles. Examination of Kaup's +holotype +in HLDH has proven this to be clearly distinct from + +Diapherodes gigantea + +but to match very well with typical ♀♀ of + +D. angulata + +from +Guadeloupe +. Comparison has proven the synonymy of Kaup's species and suggests this specimen to have originated from +Guadeloupe +. Moxey (1971: 99) erroneously synonymised + +Haplopus grayi + +with + +Diapherodes gigantea + +. + + + +Diapherodes angulata + +appears to have been moderately abundant in certain localities in +Guadeloupe +, which is seen in the good series of specimens collected by Le Moult (now in MNCN and MNHN). It has however become apparently rare and was not encountered during recent extensive collections conducted on the island in the late 1990's (Langlois & Lelong, 1997: 43). + +D. angulata + +is endemic in +Guadeloupe +and all records of + +D. gigantea + +from this island are based on misidentifications. + + + + + +Distribution ( +Fig. 381 +): + +Guadeloupe +(Basse-Terre [MNHN]; Trois Riviéres [MNHN]), endemic. + + + + +Number of specimens examined: +43 + + + +TABLE 11. +Measurements of + +Diapherodes angulata +(Fabricius, 1793) + +[mm] + + +♀, NT ♀♀ ♂♂ + +[ +MNCN +] [ +MNCN +] [ +MNCN +] + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D327FF8FFF27EA2C27501F8F.xml b/data/38/7F/30/387F3068D327FF8FFF27EA2C27501F8F.xml new file mode 100644 index 00000000000..3c68fb078bb --- /dev/null +++ b/data/38/7F/30/387F3068D327FF8FFF27EA2C27501F8F.xml @@ -0,0 +1,1149 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + +4. SUBFAMILY +CLADOMORPHINAE +BRADLEY & GALIL, 1977 + + + + +Genus eponymum: + +Cladomorphus +Gray, 1835 +: 15 + +. + + + +Cladomorphinae +Bradley & Galil, 1977 +: 186. + + +Zompro, 2004 +: 134. + + +Otte & Brock, 2005 +: 32. + + +Cladomorphidae Brunner v. Wattenwyl, 1893: 90, 98. Bacteriinae +Kirby, 1904a +: 348 (in part). + + +Kevan, 1982 +: 282 (in part). + + + +Cladoxerinae +Karny, 1923 +: 237 + +(in part). + +Diapheromerinae, +Zompro, 2001 +: 228 + +(in part). +Zompro, 2004 +: 139 (in part). + + +Phibalosomini +(SectioV: Phibalosomata) +Redtenbacher, 1908 +: 399 (in part). Phibalosominae +Günther, 1953 +: 557. + + +Phibalosomatinae, +Moxey, 1971 +: 67. + + +Xerosomatinae +, +Zompro, 2004 +: 139 (in part). + + + + +Günther (1953: 557) +established the subfamily Phibalosominae (= +Cladomorphinae +Bradley & Galil, 1977 +) for sections of + +Phibalosomini +Redtenbacher, 1908 + +and originally subdivided it into the four tribes +Cladoxerini +, +Phibalosomini +, Haplopodini and +Cranidiini +. +Bradley & Galil (1977: 186) +took over Günther's arrangement of the Phibalosominae and generally restricted themselves to translating his keys to the tribes into English. Taxonomic changes by these authors were limited to re-naming Günther's Phibalosominae to +Cladomorphinae +and Günther's tribes +Phibalosomini +, Haplopodini and +Cranidiini +to +Cladomorphini +, +Hesperophasmatini +and Craspedoniini. The new name Craspedoniini for + +Cranidiini +Günther, 1953 + +was not justified and introduced because Bradley & Galil confused the type-species of + +Craspedonia +Westwood, 1841 + +(see +Brock, 1998b +: 26), hence +Cranidiini +remains valid. The monophyly of +Cladomorphinae +sensu +Bradley & Galil, 1977 +seems poorly supported and the subfamily divides into at least two well recognized sub-divisions or clades, which do not appear particularly closely related, and indicate +Cladomorphinae +as presently recognized may not be a natural grouping (→ see comments below). + + +Zompro (2004) +introduced several major taxonomic changes within the classification of +Cladomorphinae +, which however contradict all previous opinions (e.g. +Günther, 1953 +; +Bradley & Galil, 1977 +), extensive phylogenetic studies based on morphological features (Bradler, 2009) and molecular data ( + +Whiting +et al. +, 2003 + +). The paper by +Zompro (2004) +postulates numerous questionable relationships with resulting erroneous taxonomic changes and several genera are omitted. +Zompro (2004: 135) +transferred the three genera + +Aploploides +Rehn & Hebard, 1938 + +, + +Diapherodes +Gray, 1835 + +and + +Haplopus +Burmeister, 1838 + +) from +Hesperophasmatini +to +Cranidiini +. But in fact neither genus is closely related to + +Cranidium +Westwood, 1843 + +, the type-genus of +Cranidiini +, which is proven by a wide range of morphological characters that are discussed in detail below (→ 4.2.3 and table 1). Surprisingly, the only common character for these four genera that +Zompro (2004: 135) +mentioned to justify his action is “the smooth and shining body”. The striking and numerous fundamental morphological differences between + +Cranidium + +and the other three genera were completely overlooked by +Zompro (2004: 135) +. Consequently, the exclusively Antillean + +Aploploides + +, + +Haplopus + +, + +Diapherodes + +and + +Paracranidium +Brock, 1998 + +are here removed from the South American +Cranidiini +and shown to form a well-defined clade that can be easily separated not only from +Cranidiini +but also from +Hesperophasmatini +. Therefore, Haplopodini +Günther, 1953 +(type-genus + +Haplopus +Burmeister, 1838 + +) is here re-established ( +rev. stat. +→ 5) to comprise these as well as four newly described Antillean genera. Also + +Aplopocranidium +Zompro, 2004 + +(Type-species: + +Bacteria waehneri +Günther, 1940 + +) from northwestern South +America +is not a member of +Cranidiini +as postulated by +Zompro (2004) +, but in fact shows very close relation to + +Jeremia +Redtenbacher, 1908 + +and + +Jeremiodes +Hennemann & Conle, 2007 + +, hence was transferred to +Cladomorphini +by +Hennemann & Conle (2010: 104) +. As a result, +Cranidiini +remains a monotypical tribe which only contains its type-genus, the very distinctive northeast South American + +Cranidium + +. Close relationship between +Cranidiini +to the South American +Cladomorphini +is indicated by features such as the presence of a gula in both sexes, the long and filiform gonapophyses VIII, presence of gonoplacs and a distinct praeopercular organ of ♀♀, specialized poculum of ♂♂ and the egg-morphology, which includes the presence of a median line. A new diagnosis and differentiation of +Cranidiini +is provided below (→ 4.2.3). + + +Although all genera retained in +Hesperophasmatini +by +Zompro (2004) +, namely + +Hesperophasma +Rehn, 1901 + +, + +Hypocyrtus +Redtenbacher, 1908 + +, + +Lamponius +Stål, 1875 + +, + +Rhynchacris +Redtenbacher, 1908 + +and + +Taraxippus +Moxey, 1971 + +, lack an area apicalis on the tibiae, +Zompro (2004: 139) +interpreted +Hesperophasmatini +as a subordinate taxon of the areolate subfamily +Xerosomatinae +(family +Pseudophasmatidae +). In addition to a “similar general resemblance” of the insects +Zompro (2004: 139) +mentioned common features of the extremities (“interodorsal carina of the protibiae lamelliform” and “mid- and hindlegs agree completely”) and eggs (“The eggs are bulletshaped”), stating +Hesperophasmatini +were “…simply representing derived +Xerosomatinae +, in which the area apicalis is reduced“ ( +Zompro, 2004: 139 +). As shown by Bradler (2009: 99) and confirmed herein these features do however not indicate any close relation to +Pseudophasmatidae +: +Xerosomatinae +and Zompro's placement of the tribe is not supported at all. This is also confirmed by molecular data presented by + +Whiting +et al. +(2003) + +. In fact, close relation between +Hesperophasmatini +and the here newly recognized and re-established Haplopodini, which comprises genera formerly placed in Haplopodini ( +Günther, 1953 +) or +Hesperophasmatini +respectively ( +Bradley & Galil, 1977 +), is very obvious and proven by a wide range of taxonomically and phylogenetically relevant characters of the insect and egg-morphology (→ 4.2.4). Both tribes share a distribution mainly in the West Indies with only a few taxa represented in northern Central +America +, whereas members of the +Xerosomatinae +are restricted to South and Central +America +. Consequently, +Hesperophasmatini +is here removed from +Pseudophasmatidae +: +Xerosomatinae +and transferred back to +Cladomorphinae +. A detailed discussion is presented below (→ 4.2.4). + + +Zompro (2004: 135) +transferred + +Baculini +Günther, 1953 + +from +Phasmatidae +: +Phasmatinae +to +Phasmatidae +: +Cladomorphinae +, however without providing a diagnosis or a list of genera contained. +Günther (1953: 555) +treated +Baculini +as an Oriental tribe, but because the type-genus + +Baculum +Saussure, 1861 + +was described from +Brazil +, the tribe is an exclusively New World taxon. +Baculini +is here shown to be a junior synonym of + +Cladoxerini +Karny, 1923 + +( +n. syn. +), since + +Baculum + +is a synonym of + +Cladoxerus +St. Fargeau & Audinet-Serville, 1827 + +, the type-genus of +Cladoxerini +(→ 4.2.1). + + +The striking genus + +Pterinoxylus +Audinet-Serville, 1838 + +is distributed throughout southern Central +America +, the northern portion of South +America +and also represented by one species on the southern Lesser Antilles. The genus was originally placed in Haplopodini ( +Günther, 1953: 557 +) and subsequently moved to +Hesperophasmatini +( +Bradley & Galil, 1977: 188 +). +Zompro (2004: 139) +omitted + +Pterinoxylus + +in his treatment of +Cranidiini +and +Hesperophasmatini +. Detailed examination of the insect and egg-morphology of + +Pterinoxylus + +and careful comparison with taxa of +Hesperophasmatini +and Haplopodini have revealed several features that separate it from either tribe, e.g. the tympanal region or stridulatory organ in the basal portion of the alae of ♀♀, conspicuously displaced medioventral carina of the meso- and metatibiae, longitudinal ventral keel in the basal portion of the antennae and elongate alveolar eggs, which exhibit distinct hollow, peripheral extensions on the polar-area and capitulum. Consequently, Pterinoxylini +n. trib. +is here established to contain solely the striking + +Pterinoxylus + +and a detailed discussion and justification is provided below (→ 4.2.5 and table 2). + + + +Relationships within +Cladomorphinae +( +Fig. 389 +): + +Detailed investigation and comparison of the six tribes currently contained in +Cladomorphinae +indicate the subfamily as presently treated may not form a natural group and does not support its monophyly. Based on several morphological characters of both the insects and eggs two distinct groups can be recognized within the present +Cladomorphinae +. The first group, here also regarded as the +Cladomorphinae +sensu stricto +, is formed by the principally South American +Cladomorphini ++ Cranidini + +Cladoxerini +, while the predominantly Antillean +Hesperophasmatini ++ Pterinoxylini +n. trib. ++ Haplopodini form a second fairly well distinguished and presumably monophyletic clade ( +Fig. 409 +). Examination of certain taxa currently attributed to other subfamilies (e.g. +Diapheromerinae +and +Heteronemiinae +) furthermore suggest +Cladomorphinae +sensu stricto +to be paraphyletic (Hennemann & Conle, in preparation). + + +In +Cladomorphini +and +Cranidiini +the gonapophyses VIII of ♀♀ are strongly elongated, filiform and project considerably over the apex of the anal segment ( +Figs. 8, 9 +, +16 +). Gonoplacs are present ( +Figs. 8 +, +16 +). The praeopercular organ of ♀♀ on abdominal sternum VII is very distinct and usually formed by one ( +Cranidiini +) or two to three ( +Cladomorphini +) spiniform appendages. Males have the terminal abdominal segments specialized in various ways, e.g. an elongated sometimes tube-like or remarkably enlarged and convex poculum, strongly enlarged hook-shaped or in-curving cerci or a spinose phallus. These specializations of the ♂♂ terminalia are likely to be apomorphic character states, but this deserves evaluation by a comprehensive phylogenetic study. The medioventral carina of the profemora of +Cladomorphini +is very prominent, lamellate and distinctly displaced towards the anteroventral carina and the profemora are triangular in cross-section with the anterodorsal carina conspicuously raised (♀♀ in particular). There are never sensory areas on the probasisternum or profurcasternum and both tribes have a well-developed gula. The antennae are very long and filiform with strongly elongated antennomeres. The eggs possess a median line below the micropylar plate although this is fairly different in +Cladomorphini +and +Cranidiini +. The eggs of +Cladomorphini +possess an operculum which is similar in structure to the opercula seen in genera of +Diapheromerinae +: +Diapheromerini +: “ + +Phanocles + +-group” (→ 4.2.2), being an open and hollow net-work, and all have a ± parallel-sided micropylar plate which is open internally and exhibits a distinct median line ( +Fig. 50 +). Eggs of +Cranidiini +lack the aforementioned opercular structures and have a broad ovoid micropylar plate, which has a narrowing of the posterior opening before it widens into the notch. The short median line is strongly displaced towards the polar-area ( +Fig. 49 +). The striking differential characters of +Cranidiini +are summarized below and several of these are believed to be autapomorphies of that tribe (→ 4.2.3 and +Table 1 +). + + +The position of +Cladoxerini +within the +Cladomorphinae +remains somewhat questionable, but several characters support it as the sister-taxon of +Cladomorphinae +, which consequently would place +Cranidiini +as the sister-group of +Cladomorphinae ++ +Cladoxerini +( +Fig. 409 +). Close relation to +Cladomorphini +in particular is indicated by the distinctly triangular cross-section of the profemora, which have the anterodorsal carina strongly raised and the lamellate medioventral carina considerably displaced towards the anteroventral carina. The elongated gonapophyses VIII and presence of gonoplacs in ♀♀ are shared with both +Cladomorphini +and +Cranidiini +. However, the gonapophyses VIII are increasingly less elongated and hardly project over the apex of the anal segment, which is likely to be an autapomorphy of +Cladoxerini +. The genitalia of ♂♂ do not show any significant specializations as in these two tribes, but as in +Cladomorphini +and +Cranidiini +there is a well developed gula. Also the egg-morphology supports close relations between these three tribes, the operculum bearing a capitular structure ( +Fig. 5 +) and the open internal micropylar plate having a median line. Females are always apterous and the anal fan of ♂♂ is transparent as in +Cladomorphini +and +Cranidiini +. The remarkably shortened antennae of ♀♀ ( +Fig. 3 +), which consist of no more than 30 antennomeres, and serrate posterodorsal carina of the profemora of both sexes readily distinguish the tribe from +Cladomorphini +and +Cranidiini +and might also be autapomorphies of +Cladoxerini +(→ 4.2.1). + + +Hesperophasmatini ++ Pterinoxylini +n. trib. ++ Haplopodini are likely to form a monophyletic clade that differs from +Cladomorphinae +sensu stricto +by a variety of characters. All three tribes lack gonoplacs and do not have conspicuously elongated or filiform gonapophyses VIII, these being short, not or hardly longer than gonapophyses IX and fully hidden under the anal segment. A praeopercular organ on abdominal sternum VII of ♀♀ is present, but it is much less developed and usually represented merely by a small wart-like swelling. The terminal abdominal segments of ♂♂ do not show any significant specializations and are fairly typical for +Phasmatodea +with a developed vomer. The medioventral carina of the profemora is not lamellate and more or less central on the ventral surface of the profemora. While +Hesperophasmatini +and Pterinoxylini +n. trib. +possess rough sensory-areas on the probasisternum and profurcasternum ( +Figs. 28–30 +, +41–43 +), these are lacking in Haplopodini. The presence of sensory-areas is likely to be a synapomorphy of Pterinoxylini +n. trib. ++ +Hesperophasmatini +and might support a sister-group relationship between these two tribes, which would consequently place Haplopodini as the sistergroup of these two tribes ( +Fig. 409 +). Pterinoxylini +n. trib. +is characteristic for having a tympanal region (= stridulatory organ) in the basal portion of the alae of ♀♀, which quite certainly is an autapomorphy ( +Fig. 409 +) since it is not present in any other representative of the entire subfamily. The presence of a gula in Pterinoxylini +n. trib. +appears to be plesiomorphic because it is present in all three tribes of +Cladomorphini +sensu stricto +and also distinguishes this tribe from +Hesperophasmatini +and Haplopodini. Females of all three tribes often possess shortened or vestigial wings and the anal fan of both sexes is mostly coloured, reticulate, tessellate or bears dark markings. The antennae are considerably more robust, on average shorter and less filiform than in members of +Cladomorphinae +sensu stricto +(exception +Cladoxerini +), either more or less oval in cross-section (Pterinoxylini +n. trib. +and +Hesperophasmatini +) or with the antennomeres increasingly shortened and perlamorph (Haplopodini). The eggs of all three tribes agree in aspect of the morphology of the internal micropylar plate, which is open with a large and wide posterior gap but lacks a median line as in +Cladomorphinae +sensu stricto +( +Figs. 45–48 +). The lack of a median line is likely to represent a synapomorphy of +Hesperophasmatini ++ Pterinoxylini +n. trib. ++ Haplopodini. Furthermore, eggs lack the hollow net-like structures on the operculum seen in +Cladomorphini +and have rather short, shield-shaped or anteriorly pointed micropylar plates. The internal surface of the capsule is usually shiny sepia with the micropylar plate a contrasting white. Consequently, +Hesperophasmatini ++ Pterinoxylini +n. trib. ++ Haplopodini form a well separated group within +Cladomorphinae +as currently defined and are likely to be a monophyletic clade. This hypothesis however deserves evaluation by a comprehensive phylogenetic analysis of the +Cladomorphinae +and potentially closely related taxa. + + +Previous phylogenetic analyses (e.g. + +Whiting +et al. +, 2003 + +; + +Buckley +et al. +, 2009 + +; + +Buckley +et al. +, 2010 + +) have provided support for a sister-group relationship between the +Cladomorphinae +and the tribe + +Stephanacridini +Günther, 1953 + +, an Old World clade that is today mostly restricted to some of the Pacific Islands, New +Guinea +and parts of Wallacea. This tribe is characterised by the strongly elongated gonapophyses VIII and well developed gonoplacs in ♀♀, the presence of a gula and a distinctly triangular cross-section of the profemora which has the anterodorsal carina conspicuously raised. As in most +Cladomorphinae +♀♀ of +Stephanacridini +have a strongly elongated either lanceolate or spatulate subgenital plate and ♂♂ have rather basal terminalia with a well developed vomer and a pair of thorn-pads on the posterior margin of the anal segment. Most genera of +Stephanacridini +have shortened antennae (♀♀ in particular), that often are hardly longer than the profemora. If this sister-group relationship between +Stephanacridini +and +Cladomorphinae +( +sensu lato +) supposed by e.g. + +Whiting +et al. +(2003) + +, + +Buckley +et al. +(2009) + +and + +Buckley +et al. +(2010) + +proves true, the elongated gonapophyses VIII and presence of gonoplacs in +Cladomorphinae +sensu stricto +as well as the presence of a gula in +Cladomorphinae +sensu stricto +and Pterinoxylini +n. trib. +must be regarded as plesiomorphic, while the increasingly elongated and filiform antennae in +Cladomorphini +and +Cranidiini +in particular will have to be interpreted as apomorphic. Furthermore, this hypothesis postulates a Gondwanan origin for the +Cladomorphinae +and suggests invasion of its ancestors via Gondwanan land connections from the Australasian region through +Antarctica +to South +America +perhaps during the late Cretaceous or late Tertiary. + + +In addition to a complete taxonomic revision of Haplopodini +rev. stat. +at the species level, keys to the six tribes currently in +Cladomorphinae +, brief discussions of +Cladoxerini +and +Cladomorphini +as well as detailed new descriptions and discussions of +Cranidiini +(→ 4.2.3) and Pterinoxylini +n. trib. +(→ 4.2.5) and a more detailed discussion of +Hesperophasmatini +(→ 4.2.4) appear necessary and are presented below along with lists of the genera included in each of these tribes. + + + + + + + +Tribes of +Cladomorphinae +Bradley & Galil, 1977 +: + + + + +1. + +Cladoxerini +Karny, 1923 +: 237 + +. Type-genus: + + +Cladoxerus +St. Fargeau & Audinet-Serville, 1828 + + +. = + +Baculini +Günther, 1953 +: 555 + +. Type-genus: + +Baculum +Saussure, 1862 + +. +n. syn. + + +2. +Cladomorphini +Bradley & Galil, 1977 +: 189. Type-genus: + +Cladomorphus +Gray, 1835 + +. = + +Phibalosomini +Günther, 1953 +: 557 + +. Type-genus: + +Phibalosoma +Gray, 1835 + +. + + +3. + +Cranidiini +Günther, 1953 +: 557 + +. Type-genus: + +Cranidium +Westwood, 1843 + +. + + +4. Haplopodini +Günther, 1953 +: 557 +rev. stat. +Type-genus: + +Haplopus +Burmeister, 1838 + +. + + +5. +Hesperophasmatini +Bradley & Galil, 1977 +: 188. Type-genus: + +Hesperophasma +Rehn, 1901 + +. [Here re-transferred from +Pseudophasmatidae +: +Xerosomatinae +] + + +6. Pterinoxylini +n. trib. +Type-genus: + +Pterinoxylus +Audinet-Serville, 1838 + +. + + + + + + + +4.1. Keys to the tribes of +Cladomorphinae + + + + +♀♀ + + + + +1. Body cylindrical or oval in cross-section; abdomen not considerably dilated laterally; mesosternum not tectiform......... 2 + + + +- Body strongly flattened; abdomen prominently dilated laterally ( +Fig. 13 +); mesosternum tectiform and with a granulose longitudinal median keel ( +Fig. 15 +); NE South +America +..................................................... +Cranidiini + + + + + +2. Antennae much longer than head and pronotum combined, consisting of>50 segments; profemora without serrations dorsally................................................................................................... 3 + + + +- Antennae distinctly shortened and hardly longer than head and pronotum combined, with <30 segments ( +Fig. 3 +); profemora serrate dorsally ( +Fig. 1 +); SE South +America +........................................................ +Cladoxerini + + + + + + +3. Gonapophyses VIII short, not projecting over anal segment; medioventral carina of profemora indistinct and ± central on ventral surface of femur; West Indies, Central +America +& Northern South +America +.................................... 4 + + + + +- Gonapophyses VIII elongate and projecting considerably over anal segment ( +Figs. 8–9 +); medioventral carina of profemora lamellate and strongly displaced towards anteroventral carina; South +America +.......................... +Cladomorphini + + + + + +4. No gula; alae without tympanal area; protibiae at best with single lobes dorsally; antennae round to oval in cross-section... 5 + + + +- Gula present; alae with a tympanal area (= stridulatory organ); medioventral carina of meso- and metatibiae strongly displaced towards anteroventral carina; antennae with a longitudinal median bulge ventro-basally ( +Figs. 39–40 +)... Pterinoxylini +n. trib. + + + + + + +5. With rough sensory-areas on probasisternum and/or profurcasternum ( +Figs. 28–30 +); scapus dorsoventrally flattened; profemora rectangular to trapezoidal in cross-section with anterodorsal carina at best very slightly raised....... +Hesperophasmatini + + + + +- No sensory-areas on probasisternum and profurcasternum; scapus round to oval in cross-section; profemora distinctly triangular in cross-section with anterodorsal carina conspicuously raised....................................... Haplopodini + + +♂♂ + +1. Poculum with various specializations or strongly enlarged..................................................... 2 + + + +- Poculum without specializations; small and cup or scoop-shaped................................................ 3 + + + + +2. Poculum very bulgy, strongly convex and extending ventrally by more than +2x +body diametre ( +Fig. 17 +); phallus spinulose; medioventral carina of profemora indistinct and central on ventral surface of femur; NE South +America +.......... +Cranidiini + + + + +- Poculum with two terminal teeth or posterior margin extended into a scoop, spatulate or tube-like appendage; phallus unarmed; medioventral carina of profemora distinct and displaced towards anteroventral carina; South +America +........ +Cladomorphini + + + + + + +3. Profemora shorter than head, pro- and mesonotum combined, without serrations dorsally; anal region of alae either reticulate, or plain pink to orange; West Indies, Central +America +& Northern South +America +.................................. 4 + + + + +- Profemora longer than head, pro- and mesonotum combined, serrate dorsally; anal region of alae plain/transparent ( +Fig. 7 +); SE South +America +............................................................................... +Cladoxerini + + + + + +4. With rough sensory-areas on probasisternum and/or profurcasternum; body surface dull.............................. 5 + + +- No sensory-areas on probasisternum and profurcasternum; body surface mostly ± glabrous..................Haplopodini + + + + + +5. Probasitarsus with a lobe dorsally; protibiae with the dorsal and posteroventral carinae expanded and ± lamellate or lobate; antennae with a longitudinal median bulge ventro-basally ( +Figs. 39-40 +); gula present................ Pterinoxylini +n. trib. + + + + + +- Probasitarsus simple; protibiae at best with small lobules dorsally; antennae round to oval in cross-section; no gula.............................................................................................. +Hesperophasmatini + + + +Eggs + +1. Micropylar plate circular to spear-shaped and broadened posteriorly, covering less than 2/3 of dorsal capsule surface....... 2 + + + + +- Micropylar plate elongate, slender and ± parallel-sided, covering more than 1/2 of dorsal capsule surface ( +Figs. 11–12 +, +50 +)............................................................................................ +Cladomorphini + + + + +2. Internal micropylar plate with a median line................................................................ 3 + + +- Internal micropylar plate without a median line.............................................................. 4 + + + + + +3. Capsule laterally compressed; micropylar plate small, <1/2 of capsule length; posteromedian notch of internal micropylar plate widely triangular ( +Fig. 5 +).................................................................. +Cladoxerini + + + + +- Capsule ovoid ( +Figs. 18–19 +); micropylar plate large,>1/2 of capsule length; posteromedian notch of internal micropylar plate narrowed before it widens into the gap ( +Fig. 49 +)...................................................... +Cranidiini + + + + + +4. Capsule ovoid to bullet-shaped, <2.5x longer than wide; polar-area and operculum without raised hollow extensions..... 5 + + + +- Capsule> +3x +longer than wide, alveolar; polar area and operculum with hollow, peripheral or crest-like extensions ( +Fig. 44 +)...................................................................................... Pterinoxylini +n. trib. + + + + + +5. Capsule surface and operculum covered with hairy structures ( +Figs. 22–25 +)*....................... +Hesperophasmatini + +- Capsule surface without hairy structures.......................................................... Haplopodini + +* This character only holds true for the currently known members of +Hesperophasmatini +(see → 4.2.4) + + + + + + + + +4.2. Discussion of the tribes of +Cladomorphinae +Bradley & Galil, 1977 + + + + +Below, the six tribes currently assigned to +Cladomorphinae +are discussed. New diagnoses and differentiations are presented for +Cranidiini +and Pterinoxylini +n. trib. +. Only brief discussions of +Cladoxerini +and +Cladomorphini +are provided, since both tribes appear paraphyletic and deserve more comprehensive study. +Hesperophasmatini +is discussed in more detail, but no diagnosis is provided since this would be premature and only of provisional use. The authors are aware of a large number of still undescribed species and genera of +Hesperophasmatini +, which would need to be incorporated for a meaningful description. + + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D32AFF8AFF27ED43260F1C4B.xml b/data/38/7F/30/387F3068D32AFF8AFF27ED43260F1C4B.xml new file mode 100644 index 00000000000..6a0a06facdb --- /dev/null +++ b/data/38/7F/30/387F3068D32AFF8AFF27ED43260F1C4B.xml @@ -0,0 +1,606 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + +4.2.1. + +Cladoxerini +Karny, 1923 + + + + + +( +Figs. 1–5 +) + + +Type-genus: + + +Cladoxerus +St. Fargeau & Audinet-Serville, 1828 + +: 445 + + + + +Cladoxerinae +Karny, 1923 +: 237 + +(in part). + + +Kevan, 1982 +: 283. + + + +Cladoxerini +Günther, 1953 +: 557 + +(in part). + + +Bradley & Galil, 1977 +: 189. + + +Otte & Brock, 2005 +: 32 (in part). + + + +Baculini +Günther, 1953 +: 555 + +. (Type-genus: + +Baculum +Saussure, 1861 + +) +n. syn. +Zompro, 2004 +: 134, 135. + + +Phibalosomatini (Sectio V: Phibalosomata) +Redtenbacher, 1908 +: 399 (in part). + + + +Comments: +Karny (1923: 237) +originally established the subfamily +Cladoxerinae +to replace Redtenbacher's +Phibalosomini +. +Günther (1953: 557) +first used +Cladoxerini +for a tribe of his Phibalosominae and +Bradley & Galil (1977 +: 189) listed it as a tribe of +Cladomorphinae +, while +Kevan (1982: 283) +treated it as a subfamily of his +Bacteriidae +. +Baculini +was originally established by +Günther (1953: 555) +as a tribe of +Phasmatidae +: +Phasminae +(= +Phasmatinae +Bradley & Galil, 1977 +) and included exclusively Oriental taxa. Günther's use of +Baculini +was based on the erroneous interpretation of + +Baculum +Saussure, 1861 + +by +Kirby (1904a: 327) +, who erroneously synonymised it with the Oriental + +Clitumnus +Stål, 1875 + +. In fact, +Saussure (1861: 127) +originally described + +Baculum + +as a subgenus of + +Bacillus +Latreille, 1825 + +, the type-species being the Brazilian + +Baculum ramosum +Saussure, 1861 + +by monotypy. +Kirby (1904a: 327) +erroneously selected the Sri Lankan + +Bacillus cuniculus +Westwood, 1859 + +as the type-species of + +Baculum + +, although Saussure had not included this species in the genus. Thus it was not available from the viewpoint of zoological nomenclature and cannot serve as the type-species for + +Baculum + +. Hennemann (2002) has partly clarified the confusion around the Oriental taxa erroneously assigned to + +Baculum + +and selected the Sri Lankan + +Bacillus cuniculus +Westwood + +as the type-species of + +Cuniculina +Brunner + +v. Wattenwyl, 1907, an exclusively Oriental genus. Hence, Hennemann & Conle (2008: 67) re-established +Clitumnini +Brunner v. Wattenwyl, 1893 for the Oriental genera that +Günther (1953: 555) +contained in +Baculini +. + + +Zompro (2004: 135) +discussed the genus + +Baculum + +, provided a re-description of the type-species + +B. ramosum + +, whose +type +is lost, and correctly assigned +Baculini +to the +Cladomorphinae +. However, Zompro did not identify the close relation between the newly recognized +Baculini +and +Cladoxerini +. The species which +Zompro (2004: 136, fig. 2) +described as + +Baculum ramosum + +is without any doubt congeneric with the type-species of + + +Cladoxerus +St. Fargeau & Audinet-Serville, 1828 + + +, i.e. + +C. gracilis +St. Fargeau & Audinet-Serville, 1828 + +. Hence, + +Baculum +Saussure, 1861 + +falls as a junior synonym of + +Cladoxerus + +( +n. syn. +) and the tribe +Baculini +consequently becomes a junior synonym of + +Cladoxerini +Karny, 1923 + +( +n. syn. +). + + + +FIGURES 1–5. +Tribe +Cladoxerini Karny, 1923 +. +1. + +Cladoxerus gracilis +(St. Fargeau & Audinet-Serville, 1828) + +♀: Brazil, Bahia, Santa Catharina [NHMW, No. 781]; +2. + +Cladoxerus gracilis +(St. Fargeau & Audinet-Serville, 1828) + +♂: Brazil, Bahia, Santa Catharina [NHMW, No. 781]; +3. + +Cladoxerus gracilis +(St. Fargeau & Audinet-Serville, 1828) + +♀ closeup of head showing the shortened antennae: Brazil, Espírito Santo, Linhares [RNV]; +4. + +Cladoxerus gracilis +(St. Fargeau & Audinet-Serville, 1825) + +♂ apex of abdomen: Brazil, Bahia, Santa Catharina [NHMW, No. 781]; +5. + +Cladoxerus gracilis +(St. Fargeau & Audinet-Serville, 1828) + +egg in dorsolateral view: Brazil, Sao Paulo [© B. Kneubühler]. Po = Poculum, Vo = Vomer, Cer = Cerci, ML = Micropylar line. + + + +The genus + +Parabactridium +Redtenbacher, 1908 + +(Type-species: + +Parabactridium mirum +Redtenbacher, 1908 +: 403 + +) was described on the basis of ♀♀ from +Madagascar +in MNHN and NHMW and originally placed in close relation to + + +Cladoxerus +St. Fargeau & Audinet-Serville, 1828 + + +. Hence, subsequent authors (e.g. +Bradley & Galil, 1977 +or +Otte & Brock, 2005 +) have placed the genus in the tribe +Cladoxerini +. However, the type-specimens appear to be lost and the systematic position within +Cladoxerini +has already been doubted by +Cliquennois (2005: 119) +, who hypothesized it might be related to the Madagscan tribe + +Achriopterini +Günther, 1953 + +if the type-locality given as “ +Madagascar +” was correct. Indeed, + +Parabactridium + +is most unlikely to belong in +Cladoxerini +, which is supported by certain characters mentioned in the original description by +Redtenbacher (1908: 403) +i.e. the small size (body-length including subgenital plate 90.0 mm), uni-spinose head, fairly short median segment, proportionally very short legs and abbreviated tarsi. Some of these characters rather suppose relation to the Madagascan subfamily +Antongiliinae +. Consequently, the genus is here only retained in +Cladoxerini +until its actual position is clarified. A confirmed placement of + +Parabactridium + +however remains as yet impossible. + + + + +A detailed diagnosis of the tribe would be premature, since investigation of supposedly closely related genera currently attributed to the +Heteronemiinae +: +Paraleptyniini +suggest +Cladoxerini +in its present recognition to be paraphyletic (→ see comments below). Hence, only a brief diagnosis mainly based on the type-genus + +Cladoxerus + +is provided here: + + +Members of +Cladoxerini +are well characterized and distinguished from all other five tribes currently attributed to +Cladomorphinae +by the dorsally serrate profemora of both sexes and shortened antennae, which consist of no more than 30 antennomeres. These are somewhat shorter than the profemora and have the antennomeres fairly elongate in ♂♂, while they are never considerably longer than the head and pronotum combined with the basal antennomeres strongly shortened and perlamorph in ♀♀ ( +Fig. 3 +). There are no ocelli. Both sexes are very slender and elongate stick-like insects, the ♀♀ being apterous, the ♂♂ (at least those of the type-genus + +Cladoxerus + +) having scale-like tegmina and well developed alae ( +Fig. 2 +). The anal fan of the alae of ♂♂ is transparent. Most representatives are fairly large, ♀♀ of some species achieving body lengths of up to 240.0 mm including the long subgenital plate. The body surface is usually ± smooth and sub-glabrous. Occasionally there is a pair of spines on the head of ♀♀. A well developed and fairly large gula is present. Both sexes have a long median segment that is considerably longer than the metanotum. Females have a moderately developed praeopercular organ, which is formed by a median gap or slit near the posterior margin of abdominal sternum VII, and usually is marked by two bulge-like ridges or elevations. The subgenital plate of ♀♀ is strongly elongated, lanceolate, naviculate or spatulate and projects considerably over the apex of the abdomen ( +Fig. 1 +). The gonapophyses VIII are elongated, filiform but at best slightly exceed the posterior margin of the anal segment. Gonoplacs are present and moderately elongated. Males have the vomer well developed, sclerotized and elongately triangular with a pointed terminal hook. The poculum is small and angularly cup-shaped ( +Fig. 4 +). The profemora are distinctly triangular in cross-section, with the anterodorsal carina raised and ± distinctly serrate ( +Fig. 1 +); occasionally there may also be some teeth on the posteroventral carina. The medioventral carina is lamellate and strongly displaced towards the anteroventral carina. The mid and hind legs are trapezoidal in cross-section and ± prominently armed with a variable number of teeth or lobes. The tarsi are very elongate with the basitarsus carinate dorsally with the two dorsal carinae melted with another and considerably longer than the following tarsomeres; in ♀♀ the basitarsi often have a raised dorsal carina. Eggs are fairly small, longer than wide, laterally compressed, have the polar-area flattened and the anterodorsal portion of the capsule conspicuously convex. The capsule-surface is strongly sculptured. The micropylar plate is oval and fairly small, covering less than half the length of capsule. A median line is present. The operculum bears a raised but flattened structure, which is encircled by several conspicuous carinae on the outer surface ( +Fig. 5 +). + + +The shape of the profemora, having the lamellate medioventral carina strongly displaced towards the anteroventral carina, dorsally carinate basitarsi, and the well-developed gula of both sexes, the presence of gonoplacs and the moderately elongated, filiform gonapophyses VIII of ♀♀ as well as the presence of a median line in the eggs are shared with +Cladomorphini +, which supports close relation between these two tribes and suggests a sister-group relationship between +Cladoxerini +and +Cladomorphini +( +Fig. 409 +). However, since close relation to the tribe + +Paraleptyniini +Zompro, 2004 + +(currently in +Heteronemiidae +: +Heteronemiinae +) is indicated by a good number of characters, +Cladoxerini +might by paraphyletic and any broader discussion on the true relationships of +Cladoxerini +would be premature at this point. The serrate anterodorsal carina of the profemora and increasingly shortened gonapophyses VIII of ♀♀ are likely to be autapomorphies of +Cladoxerini +. Whether the conspicuously shortened antennae of ♀♀ are plesiomorphic or apomorphic deserves further evaluation but is +a priori +interpreted as an autapomorphy of +Cladoxerini +in +Fig. 409 +, since this character is unique within +Cladomorphinae +. + + + +Distribution: +Southeastern South +America +(SE-Brazil, +Paraguay +, +Uruguay +, + +Argentina + +& +Bolivia +). + + + + + + +Genera included: + + + + + +1. +<bibRefCitation id="D447FC8FD32CFF89FF01E8BB26F01A4E" author="Cladoxerus" box="[177,664,1772,1793]" pageId="13" pageNumber="14" refString="1. Cladoxerus St. Fargeau & Audinet-Serville, 1828: 445. Type-species: Cladoxerus gracilis St. Fargeau & Audinet-Serville, 1828: 445, by monotypy. (Figs. 1 - 2)" type="journal article" year="1828"> +<emphasis id="82A25D6CD32CFF89FF01E8BB25771A4E" box="[177,287,1772,1793]" italics="true" pageId="13" pageNumber="14">Cladoxerus</emphasis> +St. Fargeau & Audinet-Serville, 1828 +</bibRefCitation> +: 445 + +. + +Type-species: +Cladoxerus gracilis +St. Fargeau & Audinet-Serville + +, +1828 +: +445 +, by monotypy. ( + +Figs. +1–2 + +) + + + += + +Baculum +Saussure, 1861 +: 127 + +. Type-species: + +Bacillus (Baculum) ramosum +Saussure, 1861 +: 127 + +, by monotypy. [Originally described as a subgenus of + +Bacillus +Latreille, 1825 + +] +n. syn. + + += + +Abrachia +Kirby, 1889 +: 503 + +. Type-species: + +Abrachia brevicornis +Kirby, 1889 + +, by monotypy. [Synonymised with + +Baculum +Saussure, 1861 + +by +Zompro, 2004 +: 135] + + += + +Ceratiscus +Caudell, 1904 +: 188 + +. Type-species: + +Ceratiscus laticeps +Caudell, 1904 + +, by original designation. [Synonymised with + +Baculum +Saussure, 1861 + +by +Zompro, 2004 +: 135] + + +2. + +Parabactridium +Redtenbacher, 1908 +: 403 + +. Type-species: + +Parabactridium mirum +Redtenbacher, 1908 +: 403 + +, by monotypy. [Presumably related to the Madagascan +Antongiliini +→ see above] + + +3. + +Wattenwylia +Toledo Piza, 1938 +: 4 + +. Type-species: + +Wattenwylia foliata +Toledo-Piza, 1938: 6 + +, by original designation. [Here transferred from +Pachymorphinae +: +Gratidiini +] + + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D32FFF94FF27E95220081874.xml b/data/38/7F/30/387F3068D32FFF94FF27E95220081874.xml new file mode 100644 index 00000000000..f4e7a769cfb --- /dev/null +++ b/data/38/7F/30/387F3068D32FFF94FF27E95220081874.xml @@ -0,0 +1,561 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +4.2.2. +Cladomorphini +Bradley & Galil, 1977 + + + + + + +( +Figs. 6–12 +, +50 +) + + + + +Type-genus: + +Cladomorphus +Gray, 1835 +: 15 + +. + + + + +Cladomorphini +Bradley & Galil, 1977 +: 189. + + +Otte & Brock, 2005 +: 32. + + +Hennemann & Conle, 2010 +: 101. + + + +Cladoxerinae +Karny, 1923 +: 237 + +(in part). + + +Cranidiini +, +Zompro, 2004 +: 134 (in part). + + +Otte & Brock, 2005 +: 32 (in part). + + +Phibalosomatini (Sectio V: Phibalosomata) +Redtenbacher, 1908 +: 399 (in part). + +Phibalosomini +Günther, 1953 +: 557 + +. + + + + +Comments: +Günther (1953: 557) +established +Phibalosomini +as a tribe of Phibalosominae (= +Cladomorphinae +Bradley & Galil, 1977 +) and distinguished it from the other three tribes in that subfamily i.e. +Cladoxerini +, Haplopodini and +Cranidiini +, either by the long antennae, ♀♀ lacking tegmina and alae or distinct medioventral carina of the profemora, which is conspicuously displaced towards the anteroventral carina. As the type-genus + +Phibalosoma +Gray, 1835 + +is a synonym of + +Cladomorphus +Gray, 1835 + +, +Bradley & Galil (1977: 188, 189) +renamed Günther's subfamily and tribe +Cladomorphinae +and +Cladomorphini +. Günther contained exclusively Neotropical genera except for the Madagascan + +Parabactridium +Redtenbacher, 1908 + +, but since the +type +specimen(s) of the typespecies + +Parabactridium mirum +Redtenbacher, 1908 + +are lost a confirmed assignment to an existing subfamily or tribe is currently impossible. Certainly however, + +Parabactridium + +is rather unlikely to be a member of +Cladomorphini +and presently attributed to +Cladoxerini +(→ 4.2.1). The genus + +Aplopocranidium +Zompro, 2004 + +was misplaced in +Cranidiini +and transferred to +Cladomorphini +by +Hennemann & Conle (2010: 104) +. + + +The strongly elongated and filiform gonapophyses VIII, which considerably project over the apex of the anal segment ( +Figs. 8–9 +), and distinct praeopercular organ ( +Fig. 8 +) are shared with ♀♀ of +Cranidiini +. The developed gonoplacs and presence of a gula are in common with +Cranidiini +and +Cladoxerini +. A sister-group relationship with +Cladoxerini +( +Fig. 409 +) is supported by the morphology of the profemora, fairly slender, stick-like body of ♀♀ and morphology of the eggs. + + +As currently recognized +Cladomorphini +appears to be paraphyletic. In particular, genera that were placed in the “ + +Phanocles + +-group” of +Diapheromeridae +: +Diapheromerinae +: +Diapheromerini +by +Zompro (2001: 195) +share numerous morphological characters that support close relation. These include the elongated and filiform gonapophyses VIII, well developed gonoplacs and distinct praeopercular organ of ♀♀, various specializations of the genitalia of ♂♂ as well as the prominent, lamellate and considerably displaced medioventral carina of the profemora and presence of a gula in both sexes. Also the egg-morphology of members of the “ + +Phanocles + +-group” supports close relationship with +Cladomorphini +, the capitulum bearing a raised hollow structure and the internal micropylar plate being open with a distinct median line. A more detailed discussion of the tribe +Cladomorphini +and revision that also covers the genera attributed to the “ + +Phanocles + +-group” by +Zompro (2001: 195) +is subject of a forthcoming study by the two first authors (Hennemann & Conle, in preparation). Since this will clarify the here suggested relationships, no broader discussion shall be presented at this point. + + + + +The following brief and certainly preliminary diagnosis of the tribe is based on the eight genera that are currently attributed to +Cladomorphini +: + + +Large to very large (♀♀ up to 245.0 mm), moderately slender to fairly stocky and robust +Cladomorphinae +with strong sexual dimorphism. Females are apterous and considerably larger than ♂♂, which are slender, stick-like insects mostly with scale-like tegmina and well developed alae (exception are the apterous ♂♂ of + +Otocraniella +Zompro, 2004 + +). The anal region of the alae is transparent grey or brown. Ocelli are lacking in both sexes. The body surface is smooth (spines of mesonotum disregarded) and slightly shiny ( + +Jeremia +Redtenbacher, 1908 + +or + +Aplopocranidium +Zompro, 2004 + +) to densely granulose ( + +Jeremiodes +Hennemann & Conle, 2006 + +or + +Cladomorphus +Gray, 1835 + +) or rugose ( + +Xylodus +Saussure, 1859 + +). The head is either elongate or oval with the vertex almost flat and unarmed ( + +Jeremiodes + +), has the vertex ± convex and either unarmed (e.g. + +Jeremia + +& + +Hirtuleius +Stål, 1875 + +), tuberculate ( + +Cladomorphus + +), or bears two prominent horns or foliaceous appendages ( + +Otocrania +Redtenbacher, 1908 + +and + +Xylodus + +). A gula is present. The antennae are filiform, longer than the mesothorax and consist of>50 antennomeres. The scapus is dorsoventrally flattened, the remaining antennomeres cylindrical. The mesothorax is elongate, at least +2x +longer than the head and pronotum combined and often armed with enlarged tubercles, spines or irregular swellings dorsally. The median segment is longer than the metanotum. Abdominal tergum V often bears crest-like posterior lobes and on sternum VII of ♀♀ there is a ± distinct praeopercular organ ( +Fig. 8 +). Occasionally, also tergites VI and VII of ♀♀ may bear posterolateral lobes. Females have the gonapophyes VIII strongly elongated, filiform and projecting considerably over the apex of the abdomen ( +Figs. 8–9 +). Gonoplacs are well developed. The subgenital plate is elongated, either lanceolate or irregularly spatulate, and extends considerably over the apex of the abdomen ( +Figs. 8–9 +). Males show conspicuous specializations of the genitalia, either having the cerci strongly enlarged and hook-like ( + +Aplopocranidium +, +Jeremia + +and + +Jeremiodes + +), the poculum apically elongated into a tube-like or spatulate appendage ( + +Cladomorphus + +, + +Otocraniella +, +Otocrania + +and + +Xylodus + +, +Fig. 10 +) or the posterior margin of the poculum with two terminal teeth ( + +Jeremiodes + +and + +Jeremia + +). The vomer is well developed and sclerotized, being a rather elongate hook-like organ with one (e.g. + +Jeremia + +and + +Jeremiodes + +) or two terminal points ( + +Cladomorphus +, +Otocraniella + +and + +Xylodus + +). The profemora are triangular in cross-section, having the anterodorsal carina raised and ± lamellate and the posterodorsal carina considerably reduced. The medioventral carina is distinct, mostly lamellate and ± conspicuously displaced towards the anteroventral carina. The meso- and metafemora and tibiae are trapezoidal in cross-section and often bear single enlarged teeth, spines or lobes. The basitarsi are carinate dorsally with the the two dorsal carinae melted with another (exceptions are + +Aplopocranidium + +and + +Jeremiodes + +). The eggs are ± laterally compressed, have a hollow, net-like capitulum and a ± elongate, roughly parallel-sided micropylar plate, which covers at least half of the dorsal capsule surface ( +Figs. 11–12 +). Internally the plate is open with a narrow posteromedian gap and a distinct but clearly separated median line ( +Fig. 50 +). + + +A well supported autapomorphy of +Cladomorphini +is represented by the conspicuous specializations of the ♂♂ genitalia, some of which are unique within the entire +Phasmatodea +(i.e. the strongly elongated and tube-like or spatulate poculum seen in + +Cladomorphus + +, + +Xylodus + +and + +Otocraniella + +, which projects considerably over the apex of the abdomen and resembles an elongated ♀ subgenital plate, +Fig. 10 +). + + + + +Distribution: +Northern half of South +America +. + + + + + + + +Genera included: + + + +1. + +Aplopocranidium +Zompro, 2004 +: 134 + +. Type-species: + +Bacteria waehneri +Günther, 1940: 456 + +, 495, by original designation of +Zompro, 2004 +: 134. + + +2. + +Cladomorphus +Gray, 1835 +: 15 + +. Type-species: + +Cladomorphus phyllinus +Gray, 1835 +: 15 + +, by subsequent designation of +Rehn, 1904 +: 61. ( +Figs. 3–8 +, +45 +) + + += + +Phibalosoma +Gray, 1835 +: 42 + +. Type-species: + +Phibalosoma lepelletieri +Gray, 1835 +: 42 + +, by monotypy. [Synonymised by +Kirby, 1904a +: 356] + + +3. + +Hirtuleius +Stål, 1875 +: 29 + +. Type-species: + +Hirtuleius laeviceps +Stål, 1875 +: 81 + +, by monotypy. + + +4. + +Jeremia +Redtenbacher, 1908 +: 425 + +. Type-species: + +Jeremia grossedentata +Redtenbacher, 1908 +: 425 + +, by monotypy. + + +5. + +Jeremiodes +Hennemann & Conle, 2007: 2 + +. Type-species: + +Jeremiodes guianensis +Hennemann & Conle, 2007: 6 + +, by original designation of Hennemann & Conle, 2007: 2. + + +6. + +Otocrania +Redtenbacher, 1908 +: 423 + +. Type-species: + +Bacteria aurita +Burmeister, 1838 +: 565 + +, by subsequent designation of Brock, 1998: 26. + + +7. + +Otocraniella +Zompro, 2004 +: 137 + +. Type-species: + +Otocraniella flagelloantennata +Zompro, 2004 +: 137 + +, by original designation of +Zompro, 2004 +: 137. + + +8. + +Xylodus +Saussure, 1859: 62 + +. Type-species: + +Xylodus adumbratus +Saussure, 1859: 62 + +, by monotypy. + + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D331FF97FF27EBDB2707182E.xml b/data/38/7F/30/387F3068D331FF97FF27EBDB2707182E.xml new file mode 100644 index 00000000000..cd51ca45260 --- /dev/null +++ b/data/38/7F/30/387F3068D331FF97FF27EBDB2707182E.xml @@ -0,0 +1,454 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +4.2.3. Tribe + +Cranidiini +Günther, 1953 + + + + + + + +( +Figs. 13–19 +, +49 +) + + + + +Type-genus: + +Cranidium +Westwood, 1843 +: 49 + +. + + + + + +Cranidiini +Günther, 1953 +: 557 + +. + + +Brock, 1998b +: 26. + +Clark-Sellick, 1998: 221. + +Zompro, 2004 +: 135 (in part). + + +Otte & Brock, 2005 +: 32 (in part). + + +Hennemann, Conle & Delfosse, 2007 +: 358 (in part). Bacteriinae +Kirby, 1904a +: 348 (in part). + + +Craspedoniini +Bradley & Galil, 1977 +: 187. [Unnecessary replacement name] +Phibalosomini +(Sectio V: Phibalosomata) +Redtenbacher, 1908 +: 399 (in part). + + + + + +Description: ♀♀/♂♂ ( +Figs. 9–10 +). + +Medium-sized to large (body lengths: ♀♀ incl. subgenital plate 107.0–161.0 mm; ♂♂ 78.0–115.0 mm), +Cladomorphinae +with remarkable sexual dimorphism. Body surface shiny, ♀♀ plain bright green. ♂♂ with short tegmina and well developed alae ( +48.2–53.2 mm +), ♀♀ apterous. ♂♂ elongate and moderately slender with body cylindrical. ♀♀ considerably larger and much broader than ♂♂, body strongly dorsoventrally flattened with meso-, metathorax and abdomen strongly laterally dilated (maximum body width 28.0–34.0 mm); body rhombic in cross-section. Head longer than wide, strongly globose and convex; vertex smooth. No ocelli. A gula is present. Antennae very long, slender and filiform, longer than head, thorax and median segment combined and consisting of>80 antennomeres. Pronotum distinctly narrower than head and mesonotum. Mesothorax of ♂♂ elongate and slender, 2.5x longer than head and pronotum combined, minutely granulose; mesosternum with a fine longitudinal median carina. Mesothorax of ♀♀ broadly and semi-circularly expanded, 1.5x longer than wide. Mesonotum strongly convex dorsally and armed with a cluster of blunt tubercles in the raised +anterior +portion; lateral margins expanded, lamellate and bluntly dentate. Mesopleurae strongly dilated, forming a longitudinal lamella with the outer margin dentate. Mesosternum strongly tectiform and with a prominent and broad, tuberculose longitudinal median keel; lateral margins slightly expanded and with a longitudinal row of tubercles ( +Fig. 15 +). Median segment distinctly longer (♂♂) or roughly equal in length to metanotum (♀♀). Abdominal segments II–VI of ♂♂ parallel-sided and distinctly longer than wide. In ♀♀ tergites and sternites II–VI with lateral margins strongly expanded and lamellate; all transverse. Praeopercular organ of ♀♀ represented by a small spiniform projection on sternum VII ( +Fig. 16 +). Epiproct and cerci of both sexes very small and considerably shorter than anal segment. Gonapophyses VIII of ♀♀ elongated, up-curving and projecting well beyond posterior margin of anal segment ( +Fig. 16 +). Gonoplacs developed ( +Fig. 16 +). Vomer of ♂♂ produced, well sclerotized and elongate-triangular. Phallus totally covered with minute black denticles. Poculum very bulgy, strongly convex and extending ventrally by more than +2x +the body width ( +Fig. 17 +). Subgenital plate of ♀♀ distinctly keeled longitudinally, boat-shaped, tapered towards a narrow ± acute apex and projecting considerably over anal segment ( +Fig. 16 +). All legs elongate and slender (♂♂) to moderately robust (♀♀), all distinctly carinate but entirely unarmed. Femora trapezoidal, tibiae almost triangular in cross-section with dorsal carinae strongly approaching each other. Profemora compressed and curved basally with posterodorsal carina reduced and considerably lower than +anterior +carina; medioventral carina distinct and roughly midways on ventral surface of femur. Medioventral carina of meso- and metafemora very faint. Tarsi simple. Basitarsi at least as long as following three tarsomeres combined and carinate dorsally with the two dorsal carinae melted with another. + + + +Eggs ( +Figs. 18–19 +, +49 +): + +Medium-sized, strongly globose and almost spherical in lateral aspect; slightly oval in cross-section. Polar-area with a wide depression. Operculum elliptical, flat and with a convex, net-like hollow expansion which covers the complete disc. Micropylar plate covering about half of capsule-length, broadly ovoid with a raised outer margin and convex central region. Internal micropylar plate open and with a narrowing of the posteromedial gap before it widens into the notch. Median line indistinct, short, very well separated from the plate and distinctly displaced towards the polar-area ( +Fig. 49 +). + + + + + +Differentiation ( +Table 1 +): + +Several features such as the presence of a gula, filiform antennae, the elongate, filiform gonapophyses VIII and presence of gonoplacs in ♀♀, specialized poculum of ♂♂ and presence of a median line in the eggs prove close relation to the South American +Cladomorphini +(→ 4.2.2). +Cranidiini +however clearly differs from +Cladomorphini +by: the shiny body surface; green general colouration; entirely unarmed legs; indistinct medioventral carina of the profemora which is roughly central on the ventral surface of the profemur; roughly trapezoidal cross-section of the profemora and very faint medioventral carina of the meso- and metafemora of both sexes. Furthermore, ♀♀ readily differ by: the strongly flattened and laterally dilated, leaf-like body; convex mesonotum and strongly longitudinally tectiform mesosternum ( +Fig. 15 +). Males are also well distinguished by the strongly enlarged and very bulgy poculum which ventrally extends by more than +2x +the body diametre, as well as the specialized phallus which is totally covered with minute black denticles. The eggs differ from those of +Cladomorphini +by having the micropylar plate oval and relatively shorter (<½ of the dorsal capsule surface) and the posteromedian notch of the plate with a narrowing before it widens into the gap ( +Fig. 49 +). + + +The completely reduced leg armature and tectiform mesosternum of both sexes, the prominently dilated mesothorax and abdomen of ♀♀ as well as the prominently enlarged poculum and spinulose phallus of ♂♂ appear to be autapomorphies of +Cranidiini +, which suggest the tribe might be the sister-group of +Cladomorphini ++ +Cladoxerini +( +Fig. 409 +) and at once distinguish it from these two tribes. The elongated gonapophyses VIII and presence of gonoplacs in ♀♀ as well as the developed gula are shared with +Cladomorphini +and +Cladoxerini +. + + +Because of the erroneous and confusing treatment of +Cranidiini +by +Zompro (2004: 135) +a detailed comparison and differentiation of +Cranidiini +and Haplopodini is presented in +Table 1 +, which emphasizes the striking differences between these two tribes and confirms the separate status of Haplopodini as well as the monotypy of +Cranidiini +. + + + +FIGURES 13–19. +Tribe +Cranidiini Günther, 1953 +. +13. + +Cranidium gibbosum +(Burmeister, 1838) + +♀: captive reared from French Guiana [coll. FH, No. 0470-11]; +14. + +Cranidium gibbosum + +♂: captive reared from French Guiana [coll. FH, No. 0470-9]; +15. + +Cranidium gibbosum + +: mesosternum of ♀ [coll. FH, No. 0470-1]; +16. + +Cranidium gibbosum + +: apex of ♀ abdomen (lateral view) [coll. FH, No. 0470-17]; +17. + +Cranidium gibbosum + +: apex of ♂ abdomen (lateral view) [coll. FH, No. 0470-19]; +18. + +Cranidium gibbosum + +: egg (dorsal view) [coll. FH, No. 0470-E]; +19. + +Cranidium gibbosum + +: egg (lateral view) [coll. FH, No. 0470-E]. Gpl = Gonoplacs, Gap8 = Gonapophyses VIII, Gap9 = Gonapophyses IX, PrOrg = Praeopercular organ, Po = Poculum, Cer = Cerci, Vo = Vomer, ML = Micropylar line. + + + +Comments: +When +Günther (1953: 557) +established the tribe +Cranidiini +, + +Cranidium +Westwood, 1843 + +was the only genus contained. A comprehensive treatment and re-description of the type-genus was presented by +Hennemann, Conle & Delfosse (2007) +. +Brock (1998b) +described a second Jamaican genus in the tribe, + +Paracranidium + +. This however, is here shown to be not closely related and to take on a rather isolated position within the re-established tribe Haplopodini +Günther, 1953 +(→ 5.6), hence is removed from +Cranidiini +. Another South American genus, + +Aplopocranidium + +, was added by +Zompro (2004: 135) +but is also not closely related to + +Cranidium + +and was transferred to +Cladomorphini +by +Hennemann & Conle (2010: 104) +who provided a comprehensive treatment of + +Aplopocranidium + +including a description of the previously unknown ♂♂. + + +Zompro (2004: 135) +removed the genera + +Aploploides +Rehn & Hebard, 1938 + +, + +Haplopus +Burmeister, 1838 + +and + +Diapherodes +Gray, 1835 + +from +Hesperophasmatini +Bradley & Galil, 1977 +and transferred them to +Cranidiini +. It is surprising that +Zompro (2004: 135) +argued the supposed close affinity of these three Antillean genera to +Cranidiini +exclusively on the fact that they have the same “smooth and shining body” and mentioned this as the only feature that in his opinion characterizes +Cranidiini +within +Cladomorphinae +. This act however is very arbitrary, since a wide range of very striking and fundamental morphological differences are present between +Cranidiini +and the mentioned three genera (→ +Table 1 +). Nor does this “feature” hold true for all taxa that Zompro transferred to +Cranidiini +, e.g. ♀♀ of + +Haplopus + +-species and ♂♂ of certain + +Diapherodes + +-species have a rather dull and ± sculptured body surface. As can be seen in +Table 1 + +Aploploides +, +Haplopus + +and + +Diapherodes + +are not at all closely related to + +Cranidium + +and here shown to form a very well separated clade, defined as the supposedly monophyletic tribe Haplopodini +rev. stat. +(→ 5.). Consequently, these three genera are here removed and +Cranidiini +is a monotypical and very well separated tribe within the subfamily +Cladomorphinae +. + + +Clark-Sellick (1998: 221, fig. 32a, b) and + +Hennemann, +Conle & Delfosse (2007 + +: 360) stated the egg of +Cranidiini +to lack a median line, although the latter authors showed there to be a median line in the illustration of the internal plate (2007: 365, fig. 12). Subsequent examination of more examples has shown a short and rather indistinct median line to be present. However, it is rather short and very well separated from the micropylar plate, being displaced towards the polar-area by more than its own length. + + +A captive reared ♀ of + +C. gibbosum + +at hand from the first author's collection (coll. FH, No. 0470-14) represents the new length record for this species, measuring 161.0 mm including the subgenital plate. + + + + +Distribution: +Restricted to Northeastern South +America +and so far recorded from Northern +Brazil +, +French Guiana +and +Suriname +( +Hennemann, Conle & Delfosse, 2007 +: 366). + + + + + + +Genus included: + + + +1. + +Cranidium +Westwood, 1843 +: 49 + +. Type-species: + +Diapherodes (Cranidium) serricollis +Westwood, 1843 +: 49 + +, pl. 6: 1 (= + +Diapherodes gibbosa +Burmeister, 1838 + +), by subsequent designation of +Bradley & Galil, 1977 +: 187. = + +Phasmilliger +Carrera, 1960 +: 100 + +. Type-species: + +Diapherodes +( +Cranidium +) +serricollis +Westwood, 1843 +: 49 + +, by indication. [Unnecessary replacement name, hence a junior objective synonym] + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D335FF9FFF27E863211C1DA8.xml b/data/38/7F/30/387F3068D335FF9FFF27E863211C1DA8.xml new file mode 100644 index 00000000000..1ca6a7d6ec6 --- /dev/null +++ b/data/38/7F/30/387F3068D335FF9FFF27E863211C1DA8.xml @@ -0,0 +1,1041 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +4.2.4. +Hesperophasmatini +Bradley & Galil, 1977 + + + + + + +( +Figs. 20–35 +, +47–48 +) + + + + +Type-genus: + +Hesperophasma +Rehn, 1901 +: 271 + +. + + + + +Hesperophasmatini +Bradley & Galil, 1977 +: 188 (in part). + +Cladoxerinae +Karny, 1923 +: 237 + +(in part). + + +Diapheromerini +“ + +Clonistria + +-group” +Zompro, 2001 +: 228 (in part). Haplopodini +Günther, 1953 +: 557 (in part). + + +Phibalosomini +(Sectio V: Phibalosomata), +Redtenbacher, 1908 +: 399 (in part). Phibalosominae, Shelford, 1908: 343, 355 (in part). + + +Phibalosomatinae, +Moxey, 1971 +: 44 (in part). + + + + +FIGURES 20–23. +Tribe +Hesperophasmatini +Bradley & Galil, 1977. +20. + +Lamponius guerini +(Saussure, 1868) + +♀: captive reared from Guadeloupe, Bassé Terre [coll. FH, No. 0084-39]; +21. + +Lamponius portoricensis +Rehn, 1903 + +♂: captive reared from Puerto Rico, Luquillo Experimental Forest [coll. FH, No. 0467-6]; +22. + +Hesperophasma planulum +(Westwood, 1859) + +♂: Dominican Republic, Province Barahona [USNM]; +23. + +Hesperophasma planulum +(Westwood, 1859) + +♀: Dominican Republic [MNCN]. + + + + +FIGURES 24–30. +Tribe +Hesperophasmatini +Bradley & Galil, 1977. +24. + +Lamponius guerini +(Saussure, 1868) + +egg (dorsolateral view): captive reared from Guadeloupe, Bassé Terre [coll. FH, No. 0084-E]; +25. + +Agamemnon cornutus +(Burmeister, 1838) + +egg (dorsal view): captive reared from Virgin Islands, Tortola [coll. FH, No. 0589-E]; +26. + +Rhynchacris ornata +Redtenbacher, 1908 + +egg (dorsal view): captive reared from S-Costa Rica, Prov. Limón [coll. FH, No. 0134-E]; +27. + +Hypocyrtus scythrus +(Westwood, 1859) + +egg (dorsolateral view): captive reared from Mexico, Veracruz, Tuxtlas [coll. FH, No. 0638-E]; +28. + +Rhynchacris ornata +Redtenbacher, 1908 + +♀: sensory-area of profurcasternum [coll. FH, No. 0134-12]; +29. + +R. ornata + +♀: left sensory area of prosternum [coll. FH, No. 0134-12]; +30. + +Hypocyrtus scythrus +(Westwood, 1859) + +♀: sensory-area of profurcasternum [coll. FH, No. 0638-1]. + + + + + +Differentiation ( +Table 2 +): + +Close relation to Pterinoxylini +n. trib. +and Haplopodini is obvious and a detailed but as yet provisional differentiation from these two tribes is presented in +Table 2 +. These three tribes are likely to represent a monophyletic clade that differs from +Cladomorphinae +sensu stricto +by a number of characters (→ see above). The differentiation can at this point only be provisional and deserves considerably more research, since the authors have at hand several as yet undescribed genera and species that would need to be incorporated for providing a sufficient and satisfying differential diagnosis (→ see comments below). Eggs of the currently known genera readily differ from both these tribes by the distinct hairy structures of the capsule and operculum ( +Figs. 24–27 +), but eggs of some of the as yet undescribed taxa have almost entirely smooth capsules. A character that is unique within this clade and the entire +Cladomorphinae +is the secondary beak-like ovipositor in ♀♀ of + +Agamemnon +Moxey, 1971 + +and + +Rhynchacris +Redtenbacher, 1906 + +, which is formed by an elongated subgenital plate and epiproct. + + +The most obvious characters that distinguish +Hesperophasmatini +from Pterinoxylini +n. trib. +are: the much smaller size (body lengths: ♀♀ 33.0–94.0 mm, ♂♂ 24.5–90.0 mm); more robust and stocky body (♀♀ in particular); rather rectangular cross-section of the profemora (distinctly triangular with the anterodorsal strongly raised in Pterinoxylini +n. trib. +); not broadly expanded and lamellate dorsal carinae of the protibiae and not displaced medioventral carina of the meso- and metafemora of both sexes. Furthermore, +Hesperophasmatini +lack developed tegmina or alae in ♀♀ and at best have very small and scale-like rudiments of alae in + +Hypocyrtus +Redtenbacher, 1908 + +. Males are either apterous, brachypterous or have fully developed alae. The presence of sensory areas on the probasisternum and/or profurcasternum ( +Figs. 28–30 +) is shared with Pterinoxylini +n. trib. +, which is likely to be a synapomorphy of Pterinoxylini +n. trib. ++ +Hesperophasmatini +. This would support a sistergroup relationship between these two tribes and distinguishes both from their possible sister-group, the Haplopodini ( +Fig. 409 +). The lack of a gula In +Hesperophasmatini +might be an autapomorphy but this deserves evaluation since this character is shared with Haplopodini. + + +From Haplopodini members of this tribe at once differ by: the generally more robust body and shorter legs (♀♀ in particular); presence of rough sensory areas on the probasisternum and/or profurcasternum (exception + +Lamponius +Stål, 1875 + +); generally more elongate antennomeres, and more rectangular cross-section of the profemora (± triangular in Haplopodini). Males of the currently known genera furthermore differ by being mostly brown or grey, while those of Haplopodini are often very colourful insects. + + + + +Comments: +No detailed and definite diagnosis of +Hesperophasmatini +is presented here, since it appears as yet premature. The authors have at hand a large number of new species and even new genera mostly from Hispaniola, whose description will be the subject of forthcoming publications. Several of these new taxa exhibit characters, which deserve comprehensive examination and evaluation and will change our present view of current +Hesperophasmatini +in various aspects. Hence, any diagnosis would now only be preliminary and cause more confusion instead of supporting the actual systematic position and clarifying the relationships of +Hesperophasmatini +within the subfamily +Cladomorphinae +. Some morphological features of the seven currently recognized genera however warrant a more detailed discussion, which is presented below. + + +Bradley & Galil (1977: 188) +established +Hesperophasmatini +to replace Haplopodini +Günther, 1953 +. +Zompro (2004: 135) +removed the genera + +Aploploides +Rehn & Hebard, 1938 + +, + +Haplopus +Burmeister, 1838 + +and + +Diapherodes +Gray, 1835 + +and erroneously placed them in the tribe +Cranidiini +(→ 4.2.3). The genera + +Hesperophasma +Rehn, 1901 + +, + +Lamponius +Stål, 1875 + +, + +Rhynchacris +Redtenbacher, 1908 + +and + +Taraxippus +Moxey, 1971 + +were retained in +Hesperophasmatini +by +Zompro (2004: 139) +, who however omitted + +Agamemnon +Moxey, 1971 + +and erroneously synonymised + +Hypocyrtus +Redtenabcher, 1908 + +with + +Lamponius + +(see below). + + +Examination has shown the monotypical genus + +Laciphorus +Redtenbacher, 1908 + +(Type-species: + +Laciphorus lobulatus +Redtenbacher, 1908 +: 351 + +) from +Peru +is not a member of +Hesperophasmatini +but belongs in +Diapheromerinae +: +Diapheromerini +, hence is here removed from +Hesperophasmatini +(→ 8.3). A redescription of + +Laciphorus + +and a discussion of its systematic position within +Diapheromerini +by the authors is in progress (Hennemann & Conle, in preparation). The monotypical + +Tersomia +Kirby, 1904 + +(Type-species: + +Tersomia brasiliensis +Kirby, 1904 + +) from +Brazil +is obviously misplaced and here removed from +Hesperophasmatini +. Females, the only sex known, are large and very slender, typically stick-like insects with a long, spatulate subgenital plate, a very short median segment, very long and slender, unarmed legs and a pair of horns between the eyes. These features as well as the remarkably short antennae, which consist of no more than 23 segments, and morphology of the genitalia place + +Tersomia + +in +Heteronemiidae +: +Heteronemiinae +: +Paraleptyniini +(→ 8.3). + + +Although lacking an area apicalis, +Zompro (2004: 139) +transferred +Hesperophasmatini +from the anareolate +Phasmatidae +: +Cladomorphinae +to the areolate +Pseudophasmatidae +: +Xerosomatinae +. The author stated they simply represented derived +Xerosomatinae +, in which the area apicalis is reduced, and postulated +Hesperophasmatini +were a subordinate taxon of +Xerosomatinae +. However, the very few features on which +Zompro (2004: 139) +based his action appear arbitrary (e.g. “eggs bullet-shaped”, “interodorsal carina of the protibiae lamelliform” and “mid- and hind legs agree completely”). Indeed, some +Hesperophasmatini +resemble certain representatives of +Xerosomatinae +: +Xerosomatini +at first glance, but presuming a close relation between these two tribes mostly based on convergences such as a similar general resemblance, basally curved and compressed profemora (a character widely distributed throughout the entire +Phasmatodea +and also typical for all members of the family +Phasmatidae +and subfamily +Cladomorphinae +respectively) and trapezoidal meso- and metafemora is the result of superficial examination. The fact that +Xerosomatini +(e.g. + +Creoxylus +Audinet-Serville, 1838 + +or + +Xylospinodes +Zompro, 2004 + +) of similar habitus occur in geographically close regions or even in the same habitats as certain +Hesperophasmatini +(e.g. + +Rhynchacris + +in Central +America +) is not at all surprising. It merely shows the “similar resemblance” discussed by +Zompro (2004: 139) +are convergent developments caused by similar or identical evolutional pressure in the common habitats of these taxa. Detailed examination and comparison of several representatives from both groups undertaken in the course of this work have revealed numerous morphological characters of the insects and eggs that clearly separate +Hesperophasmatini +not only from +Xerosomatinae +but from the entire family +Pseudophasmatidae +. This is clearly supported by phylogenetic studies based on external morphology (Bradler, 2009: 99) and molecular data ( + +Whiting +et al. +, 2003 + +; + +Buckley +et al. +, 2009 + +; + +Buckley +et al. +, 2010 + +). Bradler (2009: 99) furthermore stated that he could not find any synapomorphies that + +Lamponius +Stål, 1875 + +(the only genus of +Hesperophasmatini +this author examined) had in common with genera of +Xerosomatinae +and that none of the apomorphies of the family +Pseudophasmatidae +were present in this +Hesperophasmatini +genus. Consequently, Zompro's placement of +Hesperophasmatini +as a subordinate taxon of +Pseudophasmatidae +: +Xerosomatinae +cannot be supported and the tribe is here re-transferred back to +Cladomorphinae +, where it was originally placed by +Günther (1953: 557) +. In fact, close relation to Pterinoxylini +n. trib. +and Haplopodini is obvious and the most important characters that support the position within +Cladomorphinae +are discussed in more detail below. + + +Hesperophasmatini +is a principally Antillean taxon, with only two genera represented in Central +America +( + +Hypocyrtus +Redtenbacher, 1908 + +and + +Rhynchacris +Redtenbacher, 1908 + +). The vast number of taxa is distributed througout the West Indies and as yet only a fraction of the tribe's true diversity is known. The authors have at hand numerous new species and genera mostly from Hispaniola, which multiply the number of currently known taxa. No representatives of +Hesperophasmatini +are so far known from +the Bahamas +. + + +The northernmost distributed representative of this tribe, the Central American + +Hypocyrtus + +deserves special mention, since the genital morphology of ♂♂ differs considerably from that of all other members of +Hesperophasmatini +. While there is a well-developed and sclerotized vomer ( +Figs. 31–33 +) in ♂♂ of all other currently known genera, it is strongly reduced or missing and concealed by the paraprocts (= sternum XI) in + +Hypocyrtus + +( + +Hennemann & Conle, 2012: 66, see +Fig. 34 + +). Furthermore, the anal segment is much more tectiform than in the other genera and has the interior portions of the posterior margin facing each other and armed with prominent in-curving spines ( +Fig. 35 +). In all other genera, which do have a well-developed vomer, the posteromedian portion is merely incised and interiorly set with a variable number of small denticles. These striking genital differences are particularly remarkable, since the ♀♀ genitalia perfectly match with those of other +Hesperophasmatini +as does the insect and egg-morphology. Despite these striking differences of the external ♂♂ genital morphology and other obvious distinguishing features +Zompro (2004: 140) +erroneously synonymised + +Hypocyrtus + +with the exclusively Caribbean + +Lamponius + +. This misinterpretation was corrected by +Eilmus (2009: 30) +, who re-established + +Hypocyrtus +. + +This was confirmed by +Hennemann & Conle (2012) +, who provided a detailed revision of the genus at the species-level. The Central American + +Rhynchacris + +and the Antillean + +Agamemnon + +are the only two genera whose ♀♀ exhibit a beak-like secondary ovipositor, that is formed by the elongated subgenital plate and an elongated epiproct. The eggs of both genera are more elongate and bullet-shaped than those of other genera and instead of simply being dropped to the ground are laid into a substrate ( +Figs. 25–26 +). + + + + +Distribution: +West Indies (excluding +Bahamas +) and Central +America +, ranging from Central +Mexico +as far south as the northern portions of +Colombia +. + + + + +Below is a more detailed discussion of certain important characters, which distinguish and clearly exclude +Hesperophasmatini +from +Pseudophasmatidae +: +Xerosomatinae +: + + +1. Area apicalis: +Zompro (2004: 139) +stated that +Hesperophasmatini +strikingly “resemble” species of +Xerosomatinae +: +Xerosomatini +, and that the lack of an area apicalis on the tibiae was the only significant difference between these two tribes. The author postulated the area apicalis was merely reduced and hence interpreted the lack of this structure as an autapomorphy of +Hesperophasmatini +. However, as not only +Xerosomatinae +, but the entire family +Pseudophasmatidae +have a distinct area apicalis on all three tibiae and there are no transitions between these two extremes, +Hesperophasmatini +is, based solely on this feature, most unlikely to belong in +Pseudophasmatidae +. + + +2. Genitalia (♀♀): +The genitalia of ♀♀ of +Hesperophasmatini +differ fundamentally from those of +Xerosomatinae +by having a distinctly keeled, scoop-like subgenital plate, which is tapered towards the apex and ± distinctly projects over the apex of the abdomen. Two genera ( + +Agamemnon + +and + +Rhynchacris + +) even have the epiproct conspicuously elongated to form a beak-like secondary ovipositor together with the elongated subgenital plate. Very different specializations of the ♀ ovipositor are observed in +Xerosomatinae +. The subgenital plate is either strongly reduced, very small and scale-shaped (e.g. + +Acanthoclonia +Stål, 1875 + +, + +Metriophasma +Uvarov, 1940 + +), or slender, ± tube-like and down-curving with the lower gonapophyses enlarged and sclerotized (e.g. certain species of + +Creoxylus + +) forming a conspicuous derived appendicular ovipositor. The gonoplacs are lacking in +Hesperophasmatini +, while they are present and often conspicuously enlarged in representatives of +Xerosomatinae (Bradler, 2009: 99) +. All mentioned features do not at all support the treatment of +Hesperophasmatini +by +Zompro (2004: 139) +. Instead, the elongated subgenital plate and lack of gonoplacs are shared with Pterinoxylini +n. trib. +and Haplopodini and hence clearly prove the very close relation to these two tribes, which together form a supposedly monophyletic clade within +Cladomorphinae +( +Fig. 409 +). + + +3. Genitalia (♂♂): +Also the genital morphology of ♂♂ of +Hesperophasmatini +differs fundamentally from that of +Xerosomatini +. In +Xerosomatini +the anal segment is more or less distinctly tectiform and has the posteromedian portion sub-fissately divided with the bounding lips facing each other, labiately thickened and on their interior surfaces with several small in-curving teeth. The vomer is strongly reduced and missing (see Bradler, 2009: 99, figs. 22b–d). In contrast, +Hesperophasmatini +have the anal segment flattened and the thorn-pads at the posterior margin directed downward. The vomer is well developed, sclerotized and appearing as a roundly triangular plate usually with a single, prominent hook-like apex ( +Figs. 31–33 +, also see Bradler, 2009: 99, fig. 22a). An exception is represented by + +Hypocyrtus + +whose genital morphology resembles members of +Xerosomatini +by the tectiform anal segment and reduced vomer (see above, +Figs. 34–35 +). However this genus perfectly matches with +Hesperophasmatini +in every other aspect. These striking morphological differences of the genitalia also do not support the systematic placement of +Hesperophasmatini +suggested by +Zompro (2004: 139) +, but instead show remarkable affinity to Pterinoxylini +n. trib. +and Haplopodini and confirm the close relation to these three tribes here suggested ( +Fig. 409 +). + + +4. Sensory areas: +Most of the currently known genera of +Hesperophasmatini +(exceptions are + +Lamponius + +and + +Taraxippus + +) possess a large and well developed sensory area on the profurcasternum, an important feature completely neglected and overlooked by +Zompro (2004) +. Sometimes, two further much smaller sensory areas are present near the exavations of the procoxae on the probasisternum (e.g. + +Rhynchacris + +, +Fig. 29 +). The sensory area of the profurcasternum is often very large, slightly convex and may cover a considerable part of the segments surface ( +Figs. 28, 30 +). It is formed by a cluster of small granules or wart-like humps, each of which bears 1–5 hollow, tubelike spines or papillate evaginations. The sensory areas on the probasisternum of e.g. + +Rhynchacris + +are much smaller, consist of a single hump-like swelling and usually have the papillate evaginations relatively longer. In + +Lamponius + +these swellings of the probasisternum are present but lack the evaginations seen in + +Rhynchacris + +. The function of these sensory areas is as yet unknown, but most certainly they serve as tactile or olfactory organs, since the live insects are frequently observed rubbing their prosternum on various surfaces, such as twigs or foliage of the host plant. In addition to several other common features the presence of sensory areas on the profurcasternum and probasisternum support close relation to Pterinoxylini +n. trib. +, which corresponds to the results presented by Bradler (2009) and + +Buckley +et al. +(2009) + +(→ 4.2.5). In Pterinoxylini +n. trib. +however the sensory area of the profurcasternum is rather small, elliptical and strongly convex and the evaginations are considerably shorter than in members of +Hesperophasmatini +, being roughly cone-shaped with a deep central pit. Similar sensory areas may be present on the profurcasternum of certain members of +Xerosomatini +(e.g. some species of + +Acanthoclonia + +or + +Creoxylus + +), while there are never sensory areas on the probasisternum. The sensory areas on the profurcasternum of certain Xerosomatini-members are however rather different in structure and in contrast to +Hesperophasmatini +cover almost the complete surface of the segment, being formed by a cluster of densely arranged small, wart-like swellings, which lack any kind of evaginations or papillate structures. The different structure of the sensory areas do also not support the position of +Hesperophasmatini +supposed by +Zompro (2004: 139) +. An ultrastructural study of these sensory areas is necessary for any broader discussion on their function or importance for phylogeny (Bradler, 2009: 32). + + +5. Egg-morphology: +Zompro (2004: 139) +stated the eggs of +Hesperophasmatini +and +Pseudophasmatidae +: +Xerosomatinae +were similar in the aspect that they are “bullet-shaped”, and the micropylar plate is small, placed roughly in the “centre of the capsule” [certainly meaning centre of the dorsal egg surface] and projects from the capsule surface. These observations are surprising since eggs of +Xerosomatini +are never “bullet-shaped” as stated by +Zompro (2004: 139) +but ± ovoid. Eggs of +Hesperophasmatini +are variable in shape, ranging from distinctly elongate and bullet-like with the polar-area more or less decidedly tapered over ovoid to almost spherical. In +Xerosomatinae +the capsule surface is merely covered by ± distinctly raised, net-like structures, while the capsule surface and operculum are to a variable degree covered with conspicuous hairy structures in all currently known genera of +Hesperophasmatini +( +Figs. 24–27 +). +Xerosomatinae +have a small, roughly circular to elliptical micropylar plate, which distinctly projects from the capsule surface and is open internally with a rather narrow posteromedial gap and a distinct median line ( +Fig. 51 +). In contrast, the micropylar plate of +Hesperophasmatini +never projects considerably from the capsule surface, is relatively larger and variable in shape, being slightly transverse and shield-shaped to distinctly longer than wide with the +anterior +end narrowed and the posterior portion broadened. Internally the plate is open with a wide, triangular notch but without a median line ( +Figs. 47–48 +). Consequently, also the egg-morphology does not support the relation between +Hesperophasmatini +and +Xerosomatinae +postulated by +Zompro (2004: 139) +. Instead, the lack of a median line is shared with Pterinoxylini +n. trib. +and Haplopodini and also confirms the close relation to these two tribes revealed in the present study and also suggested by the results of Bradler (2009) and + +Buckley +et al. +(2009) + +. + + + + + +FIGURES 31–36. +Tribes +Hesperophasmatini +Bradley & Galil, 1977 and Pterinoxylini n. trib., genitalia of ♂♂. +31. + +Lamponius portoricensis +Rehn, 1903 + +: ventral view of anal segment [coll. FH, No. 0467-6]; +32. + +Agamemnon cornutus +(Burmeister, 1838) + +: ventral view of anal segment [coll. FH, No. 0589-6]; +33. + +Rhynchacris ornata +Redtenbacher, 1908 + +: ventral view of anal segment [coll. FH, No. 0134-32]; +34. + +Hypocyrtus scythrus +(Westwood, 1859) + +: ventral view of anal segment [coll. FH, No. 0638-7]; +35. + +Hypocyrtus scythrus +(Westwood, 1859) + +: caudal view of anal segment [coll. FH, No. 0638-7]; +36. + +Pterinoxylus crassus +Kirby, 1889 + +: ventral view of anal segment [coll. FH, 0588-7]. + + + + + + +Genera included: + + + +1. + +Agamemnon +Moxey, 1971 +: 71 + +. Type-species: + +Agamemnon iphimedeia +Moxey, 1971 +: 75 + +, by original designation of +Moxey, 1971 +: 71. + + +2. + +Hesperophasma +Rehn, 1901 +: 271 + +. Type-species: + +Phantasis saussurei +Bolivar, 1888 +: 137 + +, by subsequent designation of +Kirby, 1904a +: 343. [Replacement name for + +Phantasis +Saussure, 1870 + +] + + += + +Phantasis +Saussure, 1870: 188 + +. Type-species: + +Phantasis saussurei +Bolivar, 1888 +: 137 + +, by subsequent designation of +Kirby, 1904a +: 343. + + +3. + +Hypocyrtus +Redtenbacher, 1908 +: 355 + +. Type-species: + +Hypocyrtus substrumosus +Redtenbacher, 1908 +: 357 + +(= + +Hypocyrtus postpositus +Redtenbacher, 1908 + +), by subsequent designation of +Zompro, 2000 +: 95. + + +4. + +Lamponius +Stål, 1875 +: 19 + +, 74. Type-species: + +Pygirhynchus guerini +Saussure, 1868 +: 64 + +, by monotypy. = + +Antillophilus +Carl, 1913: 38 + +. Type-species: + +Antillophilus brevitarsus +Carl, 1913: 38 + +(= + +Lamponius guerini +( +Saussure, 1868 +) + +, by monotypy. + + +5. + +Rhynchacris +Redtenbacher, 1908 +: 354 + +. Type-species: + +Rhynchacris ornata +Redtenbacher, 1908 +: 354 + +, by monotypy. = + +Pseudoceroys +Hebard, 1922 +: 354 + +. Type-species: + +Pseudoceroys harroweri +Hebard, 1922 +: 355 + +, pl. 15: 1–2 by original designation. [Synonymised by +Hennemann & Conle, 2012 +: 81] + + +6. + +Tainophasma +Conle, Hennemann & Perez-Gelabert, 2014 +: 29 + +. Type-species: + +Tainophasma monticola +Conle, Hennemann & Perez, Gelabert, 2014: 31 + +, by original designation. + + +7. + +Taraxippus +Moxey, 1971 +: 67 + +. Type-species: + +Taraxippus paliurus +Moxey, 1971 +: 70 + +, by original designation of +Moxey, 1971 +: 67. + + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D33AFF9BFF27EF7D261E1CA5.xml b/data/38/7F/30/387F3068D33AFF9BFF27EF7D261E1CA5.xml new file mode 100644 index 00000000000..a8f223583aa --- /dev/null +++ b/data/38/7F/30/387F3068D33AFF9BFF27EF7D261E1CA5.xml @@ -0,0 +1,437 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + +4.2.5. Pterinoxylini n. trib. + + + + + +( +Figs. 36–44 +, +46 +) + + + + +Type-genus: + +Pterinoxylus +Audinet-Serville, 1838 +: 226 + +. + + + + +Haplopodini +Günther, 1953 +: 557 (in part). + + +Hesperophasmatini +Bradley & Galil, 1977 +: 188 (in part). + + +Phibalosomini +(Sectio V: Phibalosomata) +Redtenbacher, 1908 +: 399 (in part). + + + + + +Description: ♀♀/♂♂ ( +Figs. 37–38 +). + +Medium sized to large (body lengths: ♀♀ incl. subgenital plate 135.0–189.0 mm, ♂♂ 94.0–118.0 mm), elongate and moderately slender, stick-like, brown +Cladomorphinae +with distinct sexual dimorphism. ♂♂ with scale-like tegmina and alae exceeding abdominal tergum IV. ♀♀ brachypterous and alae with a tympanal area (= stridulatory organ) in the basal portion of the costal region; alae projecting over posterior margin of median segment. Body of ♂♂ cylindrical, of ♀♀ subcylindrical. Entire body surface ± prominently rugulose and wrinkled, thorax partly granulose or tuberculose. Mesothorax of ♂♂ occasionally spinulose. Head longer than wide, dorsoventrally flattened and ± parallel-sided. Vertex with ± prominent tubercles or spines and occasionally slightly convex ( +Figs. 39–40 +). No ocelli. A slender and transverse gula is present. Antennae moderately robust and not reaching (♀♀) or slightly projecting over posterior margin of mesothorax; consisting of 30–40 segments. Scapus dorsoventrally flattened and roundly deflexed laterally, pedicellus subcylindrical. Following antennomeres with a longitudinal median keel or bulge ventrally ( +Figs. 39–40 +). Pronotum rectangular, distinctly longer than wide and longer than head. Probasisternum with two rough sensory areas near lateral excavations of procoxae ( +Figs. 41, 43 +); profurcasternum with a raised, oval central sensory area ( +Fig. 42 +). Mesothorax elongate, at least +2x +longer than head and pronotum combined (longer in ♂♂), parallel-sided. Metanotum quadrate to slightly transverse. Meso- and metasternum as well as pleurae simple. Tegmina ovate and scale-like with a rounded central hump; slightly projecting over posterior margin of metanotum. Anal region of alae dark grey to black with ± distinct transparent spots, markings or radially arranged stripes; in ♀♀ of a conspicuous convex contour when opened. Abdomen longer than head and thorax combined. Median segment about +2x +longer than metanotum. Segments II–VI parallel-sided and either more than +2x +longer than wide (♂♂) or just indistinctly longer than wide (♀♀). Tergum VII ± laterally expanded or with a lateral lobe (♀♀ in particular). VIII–X slightly narrower (♀♀) or a little broader than previous segments (♂♂). In ♀♀ tergites III–IX often with a posteromedian tubercle. Praeopercular organ of ♀♀ indistinct and usually formed by a median tubercle close to posterior margin of sternum VII. Anal segment quadrate to slightly transverse, the posterior margin rounded with a small median indentation (♂♂) or broadly emarginated (♀♀). Epiproct small and with a longitudinal median carina; posterior margin truncate. Vomer of ♂♂ well developed, sclerotized and broadly triangular with a single short terminal hook ( +Fig. 36 +). Cerci very small, subcylindrical and slightly in-curving. Gonapophyses VIII of ♀♀ short, not extending beyond anal segment. No gonoplacs. Subgenital plate of ♀♀ elongate, irregularly naviculate or spatulate and distinctly projecting over apex of anal segment; longitudinally keeled basally but broadened and flattened towards a rounded to angular apex. Poculum of ♂♂ gently convex, cup-like and with a median carina; posterior margin notched medially. Legs short and robust (♀♀ in particular) with more or less prominently expanded or lobed carinae. Protibiae with broad foliaceous lobes and expansions (♀♀ in particular). Meso- and metafemora and corresponding tibiae with a ± distinct sub-apical dorsal lobe or tooth. Profemora shorter than mesothorax, metafemora at best reaching half way along abdominal tergum IV. Profemora compressed and curved basally and distinctly triangular in cross-section with the anterodorsal carina conspicuously raised and ± lamellate; medioventral carina indistinct and slightly displaced towards anteroventral carina. Meso- and metafemora and all tibiae trapezoidal in cross-section, the two +anterior +carinae strongly approaching each other. Medioventral carina of meso- and metafemora indistinct, and unarmed or at best with a few minute spinules. Tibiae without an area apicalis. Medioventral carina of meso- and metatibiae conspicuously displaced towards the anteroventral carina in the median portion. Tarsi short and stout, probasitarsus with a distinct rounded dorsal lobe, that is formed by the melted dorsal carinae. Meso- and metabasitarsi simple, furcate dorsally with the two dorsal carinae strongly approaching each other but well separated, and no longer than following two tarsomeres combined. + + + +FIGURES 37–44. +Tribe Pterinoxylini n. trib.. +32. + +Pterinoxylus crassus +Kirby, 1889 + +♀: captive reared from Martinique [coll. FH, No. 0588-1]; +33. + +Pterinoxylus crassus +Kirby, 1889 + +♂: captive reared from Martinique [coll. FH, No. 0588-12]; +34. + +Pterinoxylus crassus +Kirby, 1889 + +: head and pronotum of ♀ [coll. FH, No. 0588-1]; +35. + +Pterinoxylus crassus +Kirby, 1889 + +: head and pronotum of ♂ [coll. FH, No. 0588-7]; +36. + +Pterinoxylus crassus +Kirby, 1889 + +♂: Prosternum and profurcasternum showing sensory-areas (SA); +37. + +Pterinoxylus crassus +Kirby, 1889 + +♂: sensory-area of profurcasternum; +38. + +P. crassus +Kirby, 1889 + +♂: left sensory area of prosternum; +39. + +Pterinoxylus crassus +Kirby, 1889 + +egg (dorsolateral view): captive reared from Martinique [coll. FH, No. 0588-E]. + + + + +FIGURES 45–51. +Internal micropylar plates of +Cladomorphinae +and +Xerosomatinae +. +45. +Tribe Haplopodini: + +Haplopus micropterus +(St. Fargeau & Audinet-Serville, 1825) + +; +46. +Tribe Pterinoxylini +n. trib. +: + +Pterinoxylus crassus +Kirby, 1889 + +; +47. +Tribe +Hesperophasmatini +: + +Lamponius guerini +(Saussure, 1868) + +; +48. +Tribe +Hesperophasmatini +: + +Rhynchacris ornata +Redtenbacher, 1908 + +; +49. +Tribe +Cranidiini +: + +Cranidium gibbosum +(Burmeister, 1838) + +; +50. +Tribe +Cladomorphini +: + +Cladomorpus rubus +(Saussure, 1861) + +; +51. +Pseudophasmatidae +: +Xerosomatinae +: +Xerosomatini +: + +Creoxylus spinosus +(Fabricius, 1793) + +. + + + + +Eggs ( +Figs. 44 +& +46 +): + +Very large (overall length> 8.0 mm), alveolar, at least +3x +longer than wide and cylindrical to oval in cross-section. Entire capsule surface minutely punctured and strongly sculptured, with prominent raised ridges and wrinkles. Polar-area with a more or less prominent, hollow peripheral extension. Operculum circular and with a peripheral extension on outer margin similar to that of the polar-area. Micropylar plate elongate, oval and pointed anteriorly; covering about ¼ of capsule length. Micropylar cup distinct. Internal micropylar plate open with a wide, triangular posteromedian gap. No median line ( +Fig. 46 +). + + + + + +Differentiation ( +Table 2 +): + +Pterinoxylini +n. trib. +is closely related to +Hesperophasmatini +and Haplopodini, with which the increasingly shortened gonapophyses VIII and lack of gonoplacs of ♀♀ and lack of a median line in the eggs are shared. The presence of sensory areas on the probasisternum and profurcasternum are shared with +Hesperophasmatini +and support a sister-group relationship with this tribe. + + +The new tribe is characterised by: the distinctly triangular cross-section of the profemora; broadly expanded and lamellate carinae of the protibiae; dorsally lobed probasitarsus; longitudinal carina along the ventral surface of the basal antennomeres; distinctly displaced medioventral carina of the meso- and metatibiae (towards anteroventral carina); strongly laterally deflexed scapus; presence of a gula and possessing rough, oval sensory areas on both the probasisternum and profurcasternum of both sexes ( +Figs. 41–43 +). The presence of a gula is most certainly a plesiomorphic character state, because it is present in all three tribes of +Cladomorphinae +sensu stricto +, and readily distinguishes Pterinoxylini +n. trib. +from +Hesperophasmatini +and Haplopodini. Females are furthermore characterised by the conspicuous tympanal area (= stridulatory organ) in the basal portion of the alae (see discussion below), which seems to be an autapomorphy of the tribe because it is unique within the entire +Cladomorphinae +. Males are well recognized by the colouration of the anal region of the alae, which is grey to black and furnished with a variable number of transparent oval spots ( +Fig. 38 +). The eggs readily differ from those of +Hesperophasmatini +and Haplopodini by their remarkable size, very elongate and alveolar capsule which is at least +3x +longer than wide, as well as the hollow, peripheral or crest-like extensions of the polar-area and operculum ( +Fig. 44 +). + + +In addition to characters mentioned above the new tribe also differs from +Hesperophasmatini +by the much larger size as well as the considerably more elongate and slender body (♀♀ in particular). Sensory areas on the probasisternum and profurcasternum are also present in most +Hesperophasmatini +(→ 4.2.4), but the evaginations are much shorter, rather cone-shaped and have a deep central pit. + + + + +Comments: +The striking genus + +Pterinoxylus +Audinet-Serville, 1838 + +was previously included in Haplopodini by +Günther (1953) +or +Hesperophasmatini +by +Bradley & Galil (1977) +and all subsequent authors. +Zompro (2004: 139) +disregarded the genus in his newly proposed arrangement of the New World anareolate +Phasmatodea +. Detailed investigation of + +Pterinoxylus + +and comparison with +Hesperophasmatini +has revealed several characters that clearly separate the genus from this tribe. Consequently, + +Pterinoxylus + +is here removed from +Hesperophasmatini +and placed in a tribe of its own, the Pterinoxylini +n. trib. +. A detailed comparison and distinction from +Hesperophasmatini +and Haplopodini is provided in +Table 2 +below. + + + + +Distribution: +Northern half of South +America +, lower Central +America +and Lesser Antilles ( +Dominica +, +Martinique +& +Saint Lucia +). + + + +The following three interesting and taxonomically important key features warrant a more detailed recognition: + +1. Stridulatory organ. +If disturbed, live ♀♀ produce a stridulating sound, which is produced by scraping the rough basal portion of the alae by the down-curving posterior margin of the tegmina. The basal half of the prominent radial vein of the alae is dorsally covered with numerous very minute rasp-like tubercles, and together with the median and cubital vein forms a conspicuous more or less oval, sub-basal membrane or typhanal area, which is of a considerably thinner diameter than the rest of the costal region. In scraping these rasps by the sharp and hard posterior edge of the tegmina, a rustling sound is produced that is presumably increased by vibration of the tympanal area of the alae. In addition, the convex and dome-like shape of the tegmina may serve to increase the sound by resonance. This stridulating sound has so far only been reported to be produced by ♀♀, but if the alae of ♂♂ are spread a similar but much more slight sound can be observed. As in ♀♀ the radial vein of the alae is very prominent in its basal portion and covered with the same rasp-like tubercles, but interestingly no tympanal area is developed, perhaps the reason why the sound is by far not as loud as in ♀♀. + + +2. Alae of ♀♀: +In addition to exhibiting a stridulatory organ in the costal region of the alae, ♀♀ of + +Pterinoxylus + +are typical for having the anal region of a conspicuously convex contour. This makes the conventional spreading of the wings in preserved specimens almost impossible, due to the outer margin curves increasingly downward as the wing is opened. This has already been pointed out by Rehn (1957: 188, footnote 9). + + +3. Sensory areas. +The probasisternum and profurcasternum of both sexes show rough sensory areas very similar in structure to those seen in the closely related +Hesperophasmatini +, and +a priori +are homologous to the Oriental +Heteropterygidae +and certain Neotropical +Pseudophasmatidae +: +Xerosomatinae +: +Xerosomatini +. The probasisternum bears two sensory areas, one each at the excavation of the procoxae ( +Figs. 41, 43 +), and the profurcasternum has one central sensory area, which is much larger than those of the probasisternum and easily seen without magnification ( +Fig. 42 +). On the probasisternum they are formed by a conspicuous, convex and slightly transverse, white hump which dorsally bears numerous minute, cone-like evaginations each of which has a central pit or hollow. These evaginations are circular in cross-section, pale to mid brown basally and dark brown at the apex. Occasionally, there are two further, much smaller sensory areas interior of the two large outer ones. The prominent sensory area of the profurcasternum is of a slightly different structure, being formed by an oval, central cluster of rounded, whitish granules each of which bear a cluster of 2–6 of the same cone-like evaginations seen on the sensory areas of the probasisternum ( +Fig. 42 +). The function of these sensory areas is still unknown, but due to the central hollow seen in each of the numerous small evaginations, they appear to serve as tactile or olfactory organs. An ultrastructural study of these organs appears necessary for any broader discussion (Bradler, 2009: 32). + + + + + + +Genus included: + + + +1. + +Pterinoxylus +Audinet-Serville, 1838 +: 226 + +. Type-species: + +Pterinoxylus difformipes +Audinet-Serville, 1838 +: 227 + +(= + +Haplopus eucnemis +Burmeister, 1838 +: 577 + +), by monotypy. + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D33EFFA0FBE7E9DD21491FAF.xml b/data/38/7F/30/387F3068D33EFFA0FBE7E9DD21491FAF.xml new file mode 100644 index 00000000000..a37273a6305 --- /dev/null +++ b/data/38/7F/30/387F3068D33EFFA0FBE7E9DD21491FAF.xml @@ -0,0 +1,1057 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + +......continued on the next page + + + +5. REVISION OF THE +TRIBE +HAPLOPODINI +GÜNTHER, 1953 + + + + + + + + + +TABLE +2 + +. + +(Continued) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Haplopodini + +Pterinoxylini n. trib. + + +Hesperophasmatini +** + +
+Probasitarsus (♂♂) +Slender and furcate dorsally; the two dorsal carinae clearly separatedCarinate dorsally; the two dorsal carinae melted with another a forming a raised, rounded lobeSlender and furcate dorsally; the two dorsal carinae clearly separated
+Egg (Shape of capsule) +Ovoid to barrel-shaped; <2x longer than wideAlveolar with a hollow, peripheral polar extension;> 3x longer than wide (Fig. 44)Almost spherical to bullet- shaped; <2.5x longer than wide (Figs. 24–27)
+Egg (Operculum) +With a conical or knob-like central elevation or tuberculose with a raised circular rim of tuberclesWith a prominent, hollow peripheral or crest-like extension on outer margin (Fig. 39)With a circle of hair-like structures
+Distribution +West Indies, Florida Keys & Honduras (Fig. 52)Northern half of South America, lower Central America & Lesser AntillesWest Indies & Central America
+
+ + +* + +Paracranidium +Brock, 1998 + + + +** The distinction of this tribe can only be preliminary and is solely based on the few genera currently known (à see comments on +Hesperophasmatini +above) + + + + +Haplopodini +Günther, 1953 +rev. stat. + + +Type-genus: + +Haplopus +Burmeister, 1838 +: 576 + +. + + + + +Haplopodini +Günther, 1953 +: 557 (in part). + + +Bacteridae (Sectio: Bacteriae), Brunner v. Wattenwyl, 1893: 80, 83 (in part). Bacteriinae, +Kirby, 1904a +: 431 (in part). + + +Bacterinae +, +Rehn, 1904 +: 61 (in part). + + +Cladoxerinae +, +Karny, 1923 +: 130 (in part). + + +Cranidiini +, Zompro, 2005: 135 (in part). + + +Otte & Brock, 2005 +: 32 (in part). + + +Hesperophasmatini +Bradley & Galil, 1977 +: 188 (in part). +Phibalosomini +(Sectio: Phibalosomata), +Redtenbacher, 1908 +: 399. Phibalosominae, Shelford, 1908: 343, 355 (in part). Phibalosomatinae, +Moxey, 1971 +: 44 (in part). + + + + +Description: +♀♀, ♂♂: Small to very large (body lengths: ♀♀ incl. subgenital plate 50.0–197.0 mm, ♂♂ 60.0–126.0 mm), moderately slender to very robust and massive (♀♀ in particular) +Cladomorphinae +with long but thickened antennae. ♀♀ either various shades of brown and grey or bright green, ♂♂ often very colourful insects. Body cylindrical in ♂♂ and cylindrical to oval in ♀♀; in one case triangular in cross section with a prominently raised longitudinal median keel along entire dorsal body surface. Body often ± glabrous (♂♂ in particular). ♀♀ mostly brachypterous or with vestigial wings, rarely apterous, ♂♂ with scale-like tegmina and alae either well developed or shortened but rarely apterous. Head indistinctly longer than wide with the vertex ± convex and bispinose or bi-cornute; rarely flat and unarmed. No gula. No ocelli. Antennae long and projecting over mesothorax (♀♀) or median segment (♂♂); cylindrical and consisting of 55–80 segments. Antennomeres shortened indistinctly longer than wide and increasingly perlamorph; scapus slightly compressed dorsoventrally. Pro- and mesothorax to a variable degree armed with granules, tubercles or spines, rarely unarmed. Pronotum longer than wide and narrower than head. Probasisternum or profurcasternum without sensory areas. Mesothorax elongate and cylindrical (♂♂) or ± widened towards the posterior (♀♀). Mesonotum often with a cluster of tubercles or spines near +anterior +margin; in one case with a prominently semi-circularly raised longitudinal median keel. Mesopleurae of ♀♀ often ± expanded and armed with a longitudinal marginal row of tubercles, teeth or spines. Mesosternum simple. Median segment longer than metanotum (only in one case slightly shorter than metanotum). Abdomen longer than head and thorax combined. Tergites mostly unarmed but II–IV in ♀♀ may bear longitudinal carinae or single tooth- or crest-like lobes. Abdomen of ♀♀ ± swollen and broadened basally or pre-medially, segments II–VII of ± uniform width in ♂♂. Praeopercular organ of ♀♀ indistinct and formed by a longitudinal ridge or tubercle near posterior margin of sternum VII; in one case formed by a cluster of three granules ( +Figs. 326–343 +). Anal segment of ♂♂ slightly tectiform with the posterior margin rounded or roundly indented medially; posterior margin ventro-medially with a variable number of small in-curving denticles. Cerci at best equal in length to anal segment, cylindrical to oval in cross-section and ranging from straight to slightly in-curving. Vomer well developed and sclerotized, either roundly triangular or with the base semi-circular and the single terminal hook strongly elongated and papillate ( +Figs. 344–364 +). Poculum of ♂♂ convex, cup-like to conical and often with a ± distinct basal swelling or spiniform projection. Gonapophyses VIII of ♀♀ short and fully hidden under anal segment; not or hardly longer than gonapophyses IX. Gonoplacs lacking. Epiproct small, either hidden under anal segment or slightly projecting; shape ranging from triangular to semi-circular. Subgenital plate of ♀♀ ± projecting over apex of abdomen, often lanceolate or naviculate and keeled longitudinally. Legs rather short and stocky (♀♀) to moderately long and slender (♂♂), at least with small sub-apical ventral spines on the meso- and metafemora but often with additional teeth, lobes or expansions. Profemora curved and compressed basally; cross-section slightly triangular with the anterodorsal carina ± raised. Meso- and metafemora and all tibiae trapezoidal in cross-section. Medioventral carina of meso- and metafemora distinct and usually armed with a longitudinal row of spines; slightly misplaced towards anteroventral carina in profemora. Tibiae without an area apicalis. Tarsi simple and slender, probasitarsus occasionally with a rounded lobe dorsally and with the two dorsal carinae melted with another. Meso- and metabasitarsus sulacte dorsally with the two dorsal carinae well separated. All basitarsi at best as long as following three tarsomeres combined. + + + +FIGURE 52. +Map showing the distribution of the tribe Haplopodini Günther, 1953 + + + +Eggs: +Medium-sized to large, capsule ovoid or barrel-shaped. Capsule surface finely punctured to strongly coriaceous, rugulose or tuberculose. Micropylar plate at best ½ as long as capsule, shape variable. Internal micropylar plate open and with a widely triangular posteromedian notch, no median line ( +Fig. 45 +). Operculum either flat and with a circular rim of tubercles or ± conically raised to knob-like. + + + + + +Differentiation ( +Table 2 +): + +Closely related to Pterinoxylini +n. trib. +and +Hesperophasmatini +with which it shares the lack of gonoplacs and the short gonapophyses VIII of ♀♀, both characters of which are likely synapomorphies of these three tribes. On this basis and as discussed above Haplopodini possibly forms a monophyletic clade together with these two tribes within present +Cladomorphinae +sensu lato +. The lack of sensory areas on the probasisternum and profurcasternum, increasingly shortened but greater number (55–80) of antennomeres and increasingly thickened, perlamorph antennae suggest Haplopodini is the sister-taxon of Pterinoxylini +n. trib. ++ +Hesperophasmatini +( +Fig. 409 +). While the lack of sensory areas most certainly is a plesiomorphic character, the morphology of the antennae is likely to be an autapomorphy of Haplopodini. The lack of a gula is here estimated as a synapomorphy of Haplopodini + +Hesperophasmatini +. A confirmed definition of these character states however deserves a comprehensive phylogenetic analysis of the subfamily +Cladomorphinae +and supposedly closely related taxa. + +Furthermore, Haplopodini differs from both tribes by the distinct medioventral carina of the profemora which is slightly displaced towards the anteroventral carina, distinct and often spinose medioventral carina of the meso- and metafemora of both sexes, as well as the ± glabrous body surface, mostly pretty colouration and transparent orange to pink anal region of the alae of ♂♂ (either plain or reticulate). + +From Pterinoxylini +n. trib. +it also differs by: the lack of a tympanal region in the basal portion of the alae (= stridulatory organ) of ♀♀; less distinctly triangular cross-section of the profemora; not dilated or lamellate carinae of the protibiae and ovoid to barrel-shaped, much smaller eggs which lack hollow, peripheral extensions on the polar-area and operculum (→ +Table 2 +). + + +From Hesperophasmatinim, with which they share the lack of a gula, members of Haplopodini may also be distinguished by the more decidedly triangular cross-section of the profemora, longer often lanceolate or naviculate subgenital plate of ♀♀ and lack of conspicuous hairy structures in the eggs. Also, Haplopodini on average are larger and less stocky than members of +Hesperophasmatini +. + + + + +Comments: +Günther (1953: 557) +originally established the tribe Haplopodini to include some of the neotropical genera of Redtenbacher's Phibalosomatini: Sectio Phibalosomata (1908: 399) and Phibalosomatini: Sectio Eurycanthae (1908: 339), this is: + +Haplopus +Burmeister, 1838 + +, + +Diapherodes +Gray, 1835 + +, + +Pterinoxylus +Audinet-Serville, 1838 + +, + +Hesperophasma +Rehn, 1904 + +and + +Lamponius +Stål, 1875 + +. +Bradley & Galil (1977: 188) +renamed Günther's tribe +Hesperophasmatini +and added some not closely related genera ( + +Agamemnon +Moxey, 1971 + +, + +Taraxippus +Moxey, 1971 + +and + +Aploploides +Rehn & Hebard, 1838 + +). +Zompro (2004: 139) +transferred +Hesperophasmatini +from +Cladomorphinae +to +Pseudophasmatidae +: +Xerosomatinae +and placed the genera + +Haplopus + +, + +Aploploides + +, + +Diapherodes + +and + +Paracranidium + +in the distinctive South American tribe + +Cranidiini +Günther, 1953 + +. However, these four Antillean genera differ significantly from + +Cranidium +Westwood, 1843 + +, the type-genus of +Cranidiini +, and are here removed from that tribe (→ 4.2.3, +Table 1 +). Haplopodini +Günther, 1953 +is therefore reinstated to contain + +Haplopus + +, + +Aploploides + +, + +Diapherodes + +and + +Paracranidium + +as well as four newly described genera ( +rev. stat. +). These share a good number of morphological characters, which sufficiently distinguish them from +Cranidiini +, +Hesperophasmatini +or Pterinoxylini +n. trib. +and obviously form a monophyletic clade, the tribe Haplopodini (→ +Table 2 +). + + + + + +Distribution ( +Fig. 52 +): + +West Indies (Greater and Lesser Antilles, +Bahamas +), Florida Keys, +Cayman Islands +, Santanilla & Central +America +( +Honduras +). + + +Most of the Haplopodini are distributed throughout the West Indies, with only one genus ( + +Apteroplopus + + +n. gen. + +, +Fig. 377 +) represented in Central +America +(eastern +Honduras +), hence this is a principally Antillean taxon. + +Haplopus + +is restricted to the Greater Antilles, +Virgin Islands +, St. Thomas, St. Croix, Florida Keys, Dry +Tortugas +and +Bahamas +and one species is found also on the +Cayman Islands +and Swan Islands (= Santanilla, +Fig. 376 +). + +Parhaplopus + + +n. gen. + +only contains three species, one of which is endemic to +Cuba +and the other two known from Hispaniola and Gonaive +Island +( +Fig. 378 +). + +Cephaloplopus + + +n. gen. + +is represented by three species on Hispaniola and has one species on +Cuba +( +Fig. 377 +). + +Diapherodes + +is distributed throughout almost the complete Lesser and Greater Antilles, but has not yet been recorded from Hispaniola, +Cuba +or +the Bahamas +( +Figs. 375 +, +381 +). + +Paracranidium + +is restricted to the mountainous regions of East-Jamaica ( +Fig. 378 +) and the two monotypical genera + +Aploploides + +and + +Venupherodes + + +n. gen. + +are endemic to +Cuba +( +Fig. 374 +). + + + + + + +Genera included: + + + +1. + +Aploploides +Rehn & Hebard, 1938 +: 49 + +. Type-species: + +Aploploides stenocephalum +Rehn & Hebard, 1938 +: 49 + +, by original designation of +Rehn & Hebard, 1938 +: 49. + + +2. + +Apteroplopus + + +n. gen. + +Type-species: + +Dyme +grosse-tuberculata + +Brunner v. Wattenwyl, 1907: 323, by present designation. + + +3. + +Cephaloplopus + + +n. gen. + +Type-species: + +Cephaloplopus pulchellus + + +n. sp. + +, by present designation. + + +4. + +Diapherodes +Gray, 1835 +: 13 + +, 33. Type-species: + +Mantis gigantea +Gmélin, 1789 +: 2055 + +, by subsequent designation of +Kirby, 1904a +: 362. + + +5. + +Haplopus +Burmeister, 1838 +: 576 + +. Type-species: + +Cyphocrana micropterus +St. Fargeau & Audinet-Serville, 1825: 445 + +, by monotypy. = + +Aplopus +Gray, 1835 +: 13 + +, 34. + + +6. + +Paracranidium +Brock, 1998: 28 + +. Type-species: + +Diapherodes +( +Cranidium +) +pumilio +Westwoood, 1843: 50 + +, pl. 61: 2, by original designation of Brock, 1998: 28. + + +7. + +Parhaplopus + + +n. gen. + +Type-species: + +Haplopus cubensis +Saussure, 1868 +: 68 + +, by present designation. + + +8. + +Venupherodes + + +n. gen. + +Type-species: + +Platycrana venustula +Audinet-Serville, 1838 +: 242 + +, by present designation. + + + + + + + + +Keys to the genera of Haplopodini +Günther, 1953 + + + + +♀♀* + + + + +1. Wings present........................................................................................ 4 + + +- Apterous............................................................................................ 2 + + + + + +2. Body length> +6 cm +; dorsal body surface without a prominent keel nor tectiform; +Cuba +.............................. 3 + + + + +- Small insects (body < +6 cm +); dorsal body surface strongly tectiform; mesonotum with a prominent, semicircularly raised longitudinal median keel ( +Fig. 287 +); +Jamaica +( +Fig. 378 +)................................................ + +Paracranidium + + + + + + + +3. Massive insects with thorax and abdomen considerably broadened ( +Fig. 314 +); head globose and indistinctly longer than wide; vertex bi-tuberculate ( +Fig. 318 +)........................................................... + +Venupherodes + + +n. gen. + + + + + +- Slender insects ( +Fig. 53 +); head elongate and about +2x +longer than wide; vertex flat and unarmed ( +Fig. 58 +)....... + +Aploploides + + + + + + + +4. Slender insects with body cylindrical in cross-section; colour mostly brown or grey; mesothorax> 2.0x longer than head and pronotum combined; anal region of alae reticulate, with dark radial and transverse veins; not Lesser Antilles or +Jamaica +.... 5 + + + + +- Robust to very massive insects, with meso-, metathorax and basal portion of abdomen broadened; mostly bright green; body oval in cross-section; mesothorax < +2x +longer than head and pronotum combined; anal region of alae plain pink or violet; Greater & Lesser Antilles ( +Fig. 375 +).............................................................. + +Diapherodes + + + + + + + +5. Large insects (body length> +10 cm +); pair of spines on vertex extending <2/3 the height of head capsule and with a single point; abdominal tergum VII at best gently expanded or with a small posterolateral lobe.............................. 6 + + + + +- Smaller insects (body < +10 cm +); pair of spines of the vertex extending by> 2/3 the height of head capsule, crenate or multituberculate; abdominal tergum VII prominently dilated, lateral lobes extending> ½ of body width; +Cuba +& Hispaniola ( +Fig. 377 +)............................................................................... + +Cephaloplopus + + +n. gen. + + + + + + +6. Mesothorax slender and ± parallel-sided; mesonotum granulose or tuberculose; apex of subgenital plate narrow and ± pointed; probasitarsus slender; Greater Antilles, Dry +Tortugas +, Florida Keys, +Bahamas +, +Cayman Islands +and Swan Islands ( +Fig. 376 +)............................................................................................... + +Haplopus + + + +- Mesothorax swollen medially; mesonotum armed with large, blunt spine-like tubercles; apex of subgenital plate rounded or broadly truncate; probasitarsus with a lobe dorsally; only +Cuba +& Hispaniola ( +Fig. 378 +).............. + +Parhaplopus + + +n. gen. + + + +*♀♀ of + +Apteroplopus + + +n. gen. + +are not known + + +♂♂* + + + + +1. Pterous or brachypterous; median segment longer than metanotum; West Indies.................................... 2 + + + +- Apterous ( +Fig. 53 +); median segment less than half the length of the metanotum; +Honduras +( +Fig. 377 +)... + +Apteroplopus + + +n. gen. + + + + + + +2. Head globose and indistinctly longer than wide; vertex armed.................................................. 3 + + + +- Head elongate, about +2x +longer than wide; vertex flat and unarmed; +Cuba +( +Fig. 374 +)....................... + +Aploploides + + + + + + +3. Spines of vertex extending <2/3 the height of head capsule, with a single point; abdominal tergum VII parallel-sided or with a small posterolateral lobe................................................................................ 4 + + + +- Spines of the vertex extending by> 2/3 the height of head capsule, often crenate or multi-tuberculate; abdominal tergum VII strongly expanded with lateral lobe extending by> ½ of body width; +Cuba +& Hispaniola ( +Fig. 377 +)... + +Cephaloplopus + + +n. gen. + + + + + + + +4. Mesothorax> +2x +longer than head and pronotum combined; not Lesser Antilles or +Jamaica +........................... 5 + + + + +- Mesothorax < +2x +longer than head and pronotum combined; Greater & Lesser Antilles ( +Figs. 367 +)............ + +Diapherodes + + + + + + +5. Body surface dull; cerci slender, distinctly shorter than anal segment and laterally compressed; anal region of alae plain.... 6 + + + +- Body surface glabrous; cerci obtuse, ± as long as anal segment and ± cylindrical in cross-section; anal region of alae reticulate ( +Fig. 247 +); Greater Antilles, Dry +Tortugas +, Florida Keys, +Bahamas +, +Cayman Islands +and Swan Islands ( +Fig. 376 +)... + +Haplopus + + + + + + +6. Body length < +7 cm +; head globose; pronotum with a pair of +anterior +spines ( +Fig. 319 +); mesonotum only with 2–4 paired spines near +anterior +margin; +Cuba +( +Fig. 374 +)...................................................... + +Venupherodes + + +n. gen. + + + +- Body length> +8 cm +; head with vertex at best gently rounded; pronotum unarmed; complete mesonotum armed with spines; +Cuba +& Hispaniola ( +Fig. 378 +)............................................................ + +Parhaplopus + + +n. gen. + + + +*♂♂ of + +Paracranidium +Brock, 1998 + +are not known + +Eggs* + + + +1. Capsule surface strongly sculptured; no raised central capitulum................................................ 2 + + + +- Capsule surface minutely punctured or rugulose; operculum with a raised conical or knob-like central capitulum... + +Haplopus + + + + + + +2. Micropylar plate <1/3 the length of capsule................................................................. 3 + + +- Micropylar plate> 1/3 the length of capsule................................................................. 4 + + + + + +3. Micropylar plate longer than wide; heart or drop-shaped; capsule irregularly granulose and covered with fine, raised ridges ( +Figs. 312-313 +)....................................................................... + +Parhaplopus + + +n. gen. + + + + + +- Micropylar plate wider than long; shield-shaped; capsule very prominently and enevenly sculptured ( +Figs. 324–325 +)............................................................................................ + +Venupherodes + + +n. gen. + + + + + + + +4. Large (capsule length> +3.5 mm +)................................................................. + +Diapherodes + + + + + +- Small (capsule length < +3.5 mm +)........................................................ + +Cephaloplopus + + +n. gen. + + + + + + +* eggs of + +Aploploides +Rehn & Hebard, 1938 + +, + +Apteroplopus + + +n. gen. + +and + +Paracranidium +Brock, 1998 + +are not known + + + +
+
\ No newline at end of file diff --git a/data/38/7F/30/387F3068D344FFECFF27EC0D26091F57.xml b/data/38/7F/30/387F3068D344FFECFF27EC0D26091F57.xml new file mode 100644 index 00000000000..c43b6d71e80 --- /dev/null +++ b/data/38/7F/30/387F3068D344FFECFF27EC0D26091F57.xml @@ -0,0 +1,304 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Diapherodes laevicollis +(Redtenbacher, 1908) + + + + + +( +Figs. 183–189 +, +372 +) + + + + + +Diapherodes laevicollis +Redtenbacher, 1908: 434 + +. +HT +, ♀: Coll. Br. v. W., +Jamaica +, Staudinger; det. Br. v. W. + +Diapherodes laevicollis + +; 18.887 [NHMW, No. 839]. + +Moxey, 1972: 106 (in litt.). + + +Brock, 1998a: 38. +Otte & Brock, 2005: 121. + + +Aplopus +(?) + + +laevicollis +, Rehn & Hebard, 1938: 52 + +. + + + + + +Further material [ +1 ♂ +]: + + + +JAMAICA +: + + +1 ♂ +: +Jamaica +: Saint Andrew, Parrish, Hard war Gap, +26–27-VII-1985 +, C.B. & H.V. Weems, G.B. Edwards [ +FSCA +]. + + + + +Diagnosis: +Differing from the other two species in the + +jamaicensis + +species-group by the strongly laterally expanded abdominal tergum VII ( +Fig. 186 +) and strongly swollen, transverse abdominal segments II–IV of ♀♀, as well as the black scapus and pedicellus of ♂♂. It is closely related to + +D. jamaicensis +(Drury, 1773) + +but in addition to these characteristic features distinguished by: the broader body (♀♀ in particular); more robust legs and longer alae of both sexes; more blunt cephalad humps of ♀♀ as well as the broader abdominal tergum VIII ( +Fig. 188 +) and much longer terminal hook of the vomer of ♂♂ ( +Fig. 372 +). + + + + + +Description: ♀ ( +Figs. 183–184 +). + +Medium-sized (body length including subgenital plate 84.0–110.0 mm) and very massive member of the + +jamaicensis + +species-group with a distinctly widened mesothorax and abdominal segment VII; tegmina (7.0–10.0 mm) and alae (7.0–11.0 mm) rather well developed. Colour bright apple green, the meso- and metapleurae ochre with a white longitudinal stripe along lower margin. Meso- and metasternum dull green with a brownish wash, ventral surface of abdomen mostly whitish. Tegmina and costal region of alae bright green with the +anterior +margin broadly brown and interiorly bordered by a rather narrow, weakly defined yellow stripe. Anal region of alae plain pink. Antennae ochre dorsally and black ventrally. Eyes pale ochre. Tips of the +anterior +mesonotal spines dark brown. + + +Head: Indistinctly longer than wide, strongly globose, the cheeks ± parallel-sided. Vertex convex and covered with several differently sized tubercles; in centre with two prominent, conical humps, the dextral carinate and the sinistral one considerably smaller. Posterior of head with a transverse row of four distinct tubercles. Eyes of moderate size, sub-circular and their length contained just a little more than +2x +in that of cheeks. Antennae broken in the +holotype +. + + +Thorax: Pronotum about as long but narrower than head, 1.5x longer than wide and gently narrowing towards the posterior. Transverse median depression distinct, curved and almost reaching lateral margins of segment. Surface unarmed except for a pair of very low tubercles +in anterior +portion and a pair of short spines just before posterior margin. Mesothorax about 1.5x longer than head and pronotum combined, constricted anteriorly and strongly gradually widened towards the posterior. Mesonotum with a very faint longitudinal median carina and widened towards the posterior with posterior margin almost +3x +wider than +anterior +margin ( +Fig. 184 +); surface sparsely granulose, with a distinct +anterior +pair of spines and a longitudinal row of small tubercles along lateral margins. Mesopleurae with a marginal row of 10–15 spiniform tubercles or short spines; metapleurae merely with a few granules. Pro-, meso- and metasternum smooth. Tegmina broadly ovate, indistinctly longer than wide, reaching about 1/3 the way along median segment and with the central protuberance very shallow. Alae slightly longer than tegmina and reaching to posterior margin of median segment. + + + +FIGURES 183–189. + +Diapherodes laevicollis +(Redtenbacher, 1908) + +. +183. +♀ HT: Jamaica (dorsolateral view) [NHMW, No. 839]; +184. +♀ HT: Jamaica (dorsal view) [NHMW, No. 839]; +185. +♂: Jamaica, Saint Andrew, Parrish [FSCA]; +186. +♀ HT: Apex of abdomen (dorsal view—apex of subgenital plate reconstructed based on ♀ in NHMJ) [NHMW, No. 839]; +187. +♀ HT: Apex of abdomen (lateral view—apex of subgenital plate reconstructed based on ♀ in NHMJ) [NHMW, No. 839]; +188. +♂ apex of abdomen (dorsal view) [FSCA]; +189. +♂ apex of abdomen (dorsal view) [FSCA]. + + + +Abdomen: Median segment longer than metanotum, about 1.3x longer than wide and very gently widening towards the posterior; smooth. Abdomen strongly swollen sub-basally with segment II widening towards the posterior, III widest, IV–V gradually narrowing and VI almost parallel-sided. II–V wider than long, II trapezoidal and longer than III–V; these equal in length with III +2x +wider than long. VI hardly wider than VIII–X and about 1.4x wider than long. Tergum VII greatly laterally deflexed with the lateral margins rounded and almost +2x +wider than VI ( +Fig. 186 +). Tergites II–IV with two irregular converging carinae, V–VII with four roughly parallel, longitudinal carinae which are most decided on VII ( +Fig. 186 +). Sternites II–VII smooth except for a fine carina along lateral margins. Praeopercular organ formed by an elongate brown tubercle close to posterior margin of sternum VII. Tergites VIII–X narrowest segments and roughly of uniform width. VIII about ¾ the length of VII and very slightly constricted medially, about 1.3x longer than wide; IX quadrate. Anal segment a little longer than IX, with a slight longitudinal median carina and flattened towards the posterior; posterior margin rounded and entire ( +Fig. 186 +). Epiproct small and semi-circular with a keel dorsally ( +Fig. 186 +). Cerci very small, round in crosssection and tapered towards a pointed apex. Subgenital plate elongate, lanceolate, keeled longitudinally and projecting over apex of abdomen by more than the length of anal segment ( +Figs. 186–187 +). + +Legs: Profemora and mesofemora shorter than mesothorax, metatafemora reaching to posterior margin of abdominal segment IV. Medioventral carina of profemora with three small spines, of meso- and metafemora with five rather strong and back-curving spines. Posteroventral carina of meso- and metafemora with one, the anteroventral carina with two sub-apical spines. Tips of all femoral spines black. Dorsal carinae of meso- and metafemora each with a low triangular sub-apical elevation. Anterodorsal carina of protibiae slightly lamellate and undulate, in meso- and metatibiae with a shallow rounded elevation sub-basally. Basitarsi about as long as following two tarsomeres combined. Dorsal carina of probasitarsus very gently rounded. + + +♂ ( +Fig. 185 +). + +Fairly small (body length 69.0 mm) and robust for the + +jamaicensis + +species-group, body surface sub-glabrous, with very long alae (42.0 mm) that reach as far back as the posterior margin of abdominal tergum VIII. General colouration bright green, the dorsal surface of the anal segment and lateral margins of the pronotum yellow. Head yellow with a broad green postocular streak. +Anterior +margin of tegmina and the basal portion of the same region of the alae white, otherwise pale green with the veins mid green. Anal region of alae pale translucent pink. Eyes mid brown. Antennae ochraceous and becoming slightly darker towards the apex, scapus and pedicellus black. +Anterior +spines of the mesonotum black, cerci and tarsi pale creamish brown. + +Head: Globose, hardly wider than long, otherwise generally as in ♀♀ but cephalad tubercles less distinct. Eyes prominent and projecting hemispherically, their length contained hardly 1.5x in that of cheeks. Antennae projecting over posterior margin of abdominal segment II and moderately robust; with about 53 antennomeres. Scapus oval in cross-section, about 1.2x longer than wide and with the lateral margins rounded. Pedicellus cylindrical and about 2/ 3 the length of scapus, III shorter than pedicellus. + +Thorax: Pronotum about equal in length but slightly narrower than head, roundly rectangular and about 1.6x longer than wide; median transverse depression distinct, very gently curved and almost reaching lateral margin of segment. Surface smooth except for a very few minute granules; a slightly more distinct pair of granules before transverse median depression and another near posterior margin. Mesothorax 1.8x longer than head and pronotum combined. Mesonotum in front with a pair of distinct, forward-pointing spines and behind with two longitudinal rows of four spiniform tubercles which decrease in size towards the posterior; a row of small granules is present along lateral margins. Mesopleurae with a marginal row of about 10 small tubercles; metapleurae with a few small granules. Mesosternum with a few scattered granules +in anterior +portion, metasternum smooth. Tegmina oval and with a longitudinal central protuberance and reaching more than half way along median segment. Alae ± reaching to posterior margin of abdominal tergum VIII ( +Fig. 185 +). + + +Abdomen: Segments II–VII roughly of uniform width and slightly decreasing in length, all rectangular; II 2.5x and VII only about 2.2x longer than wide. Sternites II–VII smooth. Tergum VIII about ¾ the length of VII and with the lateral margins distinctly expanded and rounded ( +Fig. 188 +). IX a little shorter than VIII and very slightly narrowing towards the posterior. Anal segment about as long as IX, roughly parallel-sided, the posterior margin bilobate with a distinct median emargination ( +Fig. 188 +). Vomer with the basal portion fairly small and the terminal hook very long, slender, slightly up-curving and distinctly longer than basal portion ( +Fig. 372 +). Cerci almost as long as anal segment, slender, cylindrical and gently in-curving with the apex blunt. Poculum moderately convex, cymbiform and longitudinally carinate; roughly reaching to posterior margin of tergum IX ( +Fig. 189 +). + +Legs: Shape and armature generally as in ♀♀, but dorsal carinae of meso- and metafemora entirely smooth and tibiae not elevated sub-basally. + + + +Comments: +Redtenbacher (1908: 434) described + +Diapherodes laevicollis + +based on a unique ♀ in NHMW. The fact that only four specimens have been recorded so far suggests this distinctive species is apparently rare and considerably less abundant than the sympatric + +D. jamaicensis +(Drury, 1773) + +. Based on the record of a museum specimen, Moxey (1972: 10) stated + +H. laevicollis + +to be found on the endemic + +Eugenia alpina +(Myrtaceae) + +which might thus be a natural food-plant in +Jamaica +. Moxey (1972: 106, in litt.) recorded body lengths of 84.0–110.0 mm based on two ♀♀ in NHMJ. Eggs unknown. + + + + +Distribution: +Jamaica +: Portland, Summit of Blue Mountain Peak [NHMJ; Moxey, 1972: 106, in litt.] & Saint Andrew [FSCA]). Endemic. + + + + +Number of specimens examined: +2 + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D349FFEFFF27E85B21F31899.xml b/data/38/7F/30/387F3068D349FFEFFF27E85B21F31899.xml new file mode 100644 index 00000000000..0932cd9e762 --- /dev/null +++ b/data/38/7F/30/387F3068D349FFEFFF27E85B21F31899.xml @@ -0,0 +1,764 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + +5.5. Genus + +Haplopus +Burmeister, 1838 + + + +Type-species: + +Cyphocrana micropterus +St. Fargeau & Audinet-Serville, 1828: 445 + +, by monotypy. + + + + + +Haplopus +Burmeister, 1838: 560 + +, 576. [Emendation and replacement name for + +Aplopus +Gray, 1835 + +] +De +Haan, 1842: 107, 127. + +Westwood, 1859: 85 (in part). + + + +Saussure, +1871–1872 +: 192. + +Stål, 1875: 31. +Bolivar, 1888: 140. +Kirby, 1904a: 363 (in part). +Redtenbacher, 1908: 429 (in part). +Zompro, 2005a: 30. +Otte & Brock, 2005: 150 (in part). + + +Aplopus +Gray 1835: 34 + +. [Preoccupied by + +Aplopus +Dejean, 1821 + +( +Coleoptera +: +Curculionidae +)] Rehn, 1904: 63 (in part). + +Caudell, 1905: 83. +Rehn, 1909: 200. +Karny, 1923: 240. +Rehn & Hebard, 1938: 52. +Adams & Adams, 1982: 263. +Brock, 1998c: 33. + + + +<emphasis id="82A25D6CD348FFEDFF27EF1025651C13" box="[151,269,327,348]" italics="true" pageId="105" pageNumber="106">Cyphocrana</emphasis> +, St + +. +Fargeau & Audinet-Serville +, +1828 +: +445 +. +Diapherodes +Gray, +1835 +: 33 +(in part) +. + + + +Moxey, 1972: 85 (in litt.; in part). [As a synonym of + +Aplopus +Gray, +1835 + +in error] + +Phasma +, Stoll, 1813: 61 + +& 1788: pl. 21: 77 (♀). [ +Not: + +Haplopus +, Shelford, 1908: 355 + +, 365. → + +Pterinoxylus +Audinet-Serville, 1838 + +] + + +Description: ♂♂, ♀♀. +Medium-sized to large (body length ♀♀ (including subgenital plate) 115.5–172.0 mm, ♂♂ 82.0–103.0 mm), slender and elongate Haplopodini, ♀♀ brachypterous, ♂♂ brachypterous or with well developed alae. Body ± cylindrical in cross-section. Colouration of ♀♀ various shades of brown, straw and grey, rarely greenish. ♂♂ rather colourful insects and sometimes multi-colorous but mostly green or greenish brown; body surface glabrous. Head indistinctly longer than wide and globose, vertex ± convex and distinctly bi-spinose or bicornute; the dextral spine larger than the sinistral. Antennae filiform in ♀♀ and considerably thickened and robust in ♂♂; in ♀♀ almost as long as head and complete thorax combined, in ♂♂ reaching at least to abdominal segment III. Pronotum about as long as head and with a ± distinct pair of +anterior +tubercles or spines; otherwise ± tuberculose. Mesothorax elongate and parallel-sided, at least +2x +longer than head and pronotum combined. Mesonotum in ♀♀ rather irregularly and to a variable degree armed with granules or spiniform tubercles, in ♂♂ armed with a variable number of distinct spines. Mesopleurae smooth in ♂♂ and with a longitudinal row of tubercles in ♀♀. Meso- and metasternum irregularly set with a variable number of granules or tubercles; metasternum may be smooth in ♂♂. Tegmina broadly oval and with a moderately distinct central hump in ♂♂; ± reaching posterior margin of metanotum. Alae of ♀♀ ± as long as tegmina; of ♂♂ variable, either slightly shorter than tegmina or reaching as far as abdominal segment VI. Anal region reticulate with distinct brown to black radial and transverse veins, translucent pink or red in ♂♂. Abdomen considerably longer than head and thorax combined. Median segment longer than metanotum, smooth. Segments II–VII distinctly longer than wide. Tergites unarmed in ♂♂, II–V often with a ± distinct pair of posterior spines in ♀♀. VII parallel-sided, with lateral margins gently rounded posteriorly, or with a small posterolateral lobe or tooth. VIII and IX narrower (♀♀) or slightly wider (♂♂) than previous segments. Sternites II–VII smooth. Praeopercular organ of ♀♀ formed by a ± distinct, elongate and longitudinal wart-like median tubercle close to posterior margin of sternum VII ( +Figs. 288–289 +). Anal segment with a longitudinal median carina and the posterior margin with a ± distinct median notch; tapered in ♀♀. Epiproct very small in ♂♂, triangular or shield-shaped and ± projecting beyond anal segment in ♀♀. Vomer of ♂♂ well developed, broadened basally and with an elongate, ± papillate terminal hook ( +Figs. 304–310 +). Cerci straight, small and tapered in ♀♀, obtuse, about as long as anal segment and cylindrical in ♂♂. Poculum of ♂♂ convex, cup-like, often longitudinally carinate and with a blunt hump or spine basally. Subgenital plate of ♀♀ long, ± lanceolate with the apex narrow and ± pointed; projecting over apex of abdomen by at least the combined length of tergites IX and X. Legs of moderate length, pro- and mesofemora shorter than mesothorax in ♀♀, about as long or a little longer in ♂♂. +Hind +legs ± reaching (♂♂) or clearly not reaching (♀♀) to the apex of abdomen. Two outer ventral carinae of meso- and metafemora each with 1–3 sub-apical spines, the medioventral carina of these femora with a longitudinal row of 4–7 ± distinct spines. Dorsal carinae of all femora unarmed, those of the meso- and metafemora often forming a shallow to acutely triangular sub-apical tooth or lobe. Tibiae unarmed except for a few small teeth in the apical portion of the medioventral carina; anterodorsal carina in ♀♀ sometimes gently elevated sub-basally and sub-apically. All basitarsi slender and rather elongate, longer than following two tarsomeres combined. + + +Eggs: +Medium-sized (capsule length +3.1–4.4 mm +), capsule ovoid, round in cross-section and> 1.5x longer than wide, polar area rounded. Capsule surface minutely granulose or rugulose. Micropylar plate elongately heartshaped, the +anterior +end narrowed and the widened posterior end with a prominent median notch;> 2/3 as long as capsule. No median line ( +Fig. 40 +). Operculum with a prominent, raised, squamiform, hat or knob-like capitulum. Colouration of capsule variable, often prettily mottled in various shades of brown, straw, cream, grey and orange. + + +Differentiation: +Very close to + +Parhaplopus + + +n. gen. + +but differing by: the convex and distinctly bi-cornute vertex and +anterior +pair of tubercles or spines on the pronotum of both sexes; slender mesothorax and slender probasitarsus of ♀♀, as well as the reticulate anal region of the alae; larger and conspicuously thickened cerci and more convex poculum with a ± distint central spine of ♂♂. The eggs clearly differ from those of + +Parhaplopus + + +n. gen. + +by having the capsule surface much less sculptured and possessing a ± distinct conical, hat or knob-like capitulum. For a more detailed differentiation see +Table 29 +. + + + + +Comments: +Burmeister (1838: 576) established + +Haplopus + +as an amendment to + +Aplopus +Gray, 1835 + +based on the original Greek pronounciation. This was however an unjustified emendation (ICZN, 1999: Article 32.5) and hence + +Haplopus + +is a junior objective synonym of + +Aplopus +Gray + +(ICZN, 1999: Article 33.2.3). + +Aplopus +Gray, 1835 + +however is preoccupied and a junior homonym of + +Aplopus +Dejean, 1821 + +( +Coleoptera +: +Curculionidae +) and therefore replaced by + +Haplopus +Burmeister, 1838 (Zompro, 2005a: 30) + +, which is an available name (ICZN, 1999: Article 19.1). + + +In the composition it was used by most former authors (e.g. Kirby, 1904a; Redtenbacher, 1908 or Moxey, +1972 in +litt.) + +Haplopus +Burmeister, 1838 + +was not a natural grouping, which had already been suggested by Rehn & Hebard (1938: 52). This is obviously seen in two clearly distinct +types +of eggs and several obvious distinctive features of the insects. Eggs of typical + +Haplopus + +exhibit a more or less prominently conical, knob or hat-like capitulum and have a rather faintly coriaceous capsule surface, whereas those of the second group lack a central capitulum and have the capsule surface prominently sculptured with raised ridges and humps. Species belonging to the second group are here transferred to the “ + +jamaicensis + +species-group” of + +Diapherodes +Gray, 1835 + +. + + +One species formerly attributed to + +Haplopus + +, i.e. + +Haplopus dubius +(Gray, 1835) + +, is definitely misplaced and here removed from the genus. The exact systematic position however remains uncertain (→ 5.9). + + + + + +Distribution ( +Fig. 376 +): + +Bahamas +, Florida Keys, Dry +Tortugas +, Greater Antilles (Hispaniola and +Puerto Rico +), Gonaive, Mona +Island +east of Hispaniola, +Navassa Island +west of Hispaniola, +Virgin Islands +(St. Croix, St. Thomas, +St. John +, +Anegada +, Guana, Little Thatch, Moskito and +Tortola +), +Cayman Islands +and Swan Islands. Although no definite records are available so far, the genus is most certainly also represented on the +Caicos Islands +north of Hispaniola ( +Fig. 312 +). + + + + + + +Species included: + + + +1. + +Haplopus bicuspidatus +de Haan, 1842: 128 + +. + +[Distribution: Hispaniola] + +2. + +Haplopus brachypterus + + +n. sp. + + +[Distribution: Hispaniola] + +3. + +Haplopus intermedius + + +n. sp. + + +[Distribution: Hispaniola] + +4. + +Haplopus micropterus +(St. Fargeau & Audinet-Serville, 1828: 445) + +[ + +Cyphocrana + +]. = + +Phasma angulata +Stoll, 1813: 61 + +, pl. 21: 77 (♀). = + +Haplopus bituberculatum +de Haan, 1842: 128 + +. +n. syn. += + +Haplopus cythereus +Westwood, 1859: 86 + +, pl. 18: 5, 5a & b (♂). +n. syn. += + +Haplopus ligiolus +Redtenbacher, 1908: 432 + +. +n. syn. += + +Haplopus ligia +Westwood, 1859: 89 + +, pl. 1: 1, 1a, 1b (♂) & 2, 2a (♀). +n. syn. += + +Haplopus obtusus +Redtenbacher, 1908: 431 + +. +n. syn. += + +Diapherodes spinipes +Gray, 1835: 34 + +. +n. syn. + + +[Distribution: Hispaniola, Mona Id., +Puerto Rico +, St. Croix & +Virgin Islands +] + + +5. + +Haplopus scabricollis +(Gray, 1835: 34) + +[ + +Diapherodes + +]. = + +Aplopus mayeri +Caudell, 1905: 83 + +. +n. syn. += + +Aplopus similis +Caudell, 1904: 65 + +. +n. syn. + + +[Distribution: +Bahamas +, S-Florida, Florida Keys, Dry +Tortugas +, +Navassa +Id., +Cayman +Ids. & Swan Ids.] + + +6. + +Haplopus sobrinus + + +n. sp. + + + +[Distribution: +Cuba +] + + +7. + +Haplopus woodruffi + + +n. sp. + + + +[Distribution: +Cayman Islands +( +Cayman +Brac)] + + + + + + + + +Keys to the species of + +Haplopus + + + + + +♀♀ + + + + +1. Vertex convex; alae as long as or longer than tegmina and covering> 2/3 of median segment.......................... 4 + + +- Vertex gently rounded; alae at best equal in length to tegmina and covering at best ½ of median segment................ 2 + + + + +2. Spines of the vertex blunt or obsolete; anal region of alae not red................................................ 3 + + + +- Spines of the vertex acute ( +Fig. 268 +); alae much shorter than tegmina and covering only 1/3 of median segment, anal region red; epiproct distinct, shield-shaped ( +Fig. 273 +); +Bahamas +, Florida Keys, Dry +Tortugas +, +Navassa Island +, +Cayman Islands +& Swan Islands................................................................................. + +scabricollis + + + + + + + +3. Spines of the vertex obsolete ( +Fig. 277 +); tegmina distinctly shorter than alae and covering only 1/3 of median segment ( +Fig. 278 +), anal region reticulate; epiproct acutely triangular and keeled dorsally; +Cuba +........................ + +sobrinus + + +n. sp. + + + + + +- Spines of the vertex blunt ( +Fig. 281 +); alae subequal in length to tegmina and covering about ½ of median segment, anal region pale transparent pink; epiproct very small ( +Fig. 283 +); +Cayman +Brac.................................. + +woodruffi + + +n. sp. + + + + + + +4. Abdominal tergum VII parallel-sided; epiproct small, triangular; only Hispaniola................................... 5 + + +- Abdominal tergum VII ± broadened / expanded, or with a lobe posterolaterally; epiproct distinct....................... 6 + + + + + +5. Epiproct very small; anal segment with a shallow concave excavation posteromedially ( +Fig. 208 +); profurcasternum tuberculate..................................................................................... + +brachypterus + + +n. sp. + + + + + +- Epiproct acutely triangular; anal segment with a distinct, triangular posteromedian incision ( +Fig. 197 +); profurcasternum smooth.................................................................................... + +bicuspidatus + + + + + + + +6. Epiproct roundly triangular to semi-circular, ± shield-shaped ( +Figs. 241–242 +); mesonotum <2.3x longer than head and pronotum combined; alae covering> ¾ of median segment; antennae red ventrally............................. + +micropterus + + + + + + +- Supraanal plate acutely triangular ( +Fig. 215 +); mesonotum 2.4x longer than head and pronotum combined; alae covering <¾ of median segment; antennae brown........................................................... + +intermedius + + +n. sp. + + + + +♂♂ + +1. Brachypterous, alae not reaching to apex of median segment................................................... 2 + + + +- Alae well-developed, exceeding abdominal tergum IV........................................................ 5 + + + + +2. Large (body> +80 mm +); horns of the head prominent and acute; three terminal abdominal segment scarcely broader than previous; tergum VII with a posterolateral tooth or lobe........................................................... 3 + + + + +- Small (body < +80 mm +); horns of the head very small and blunt ( +Fig. 282 +); three terminal abdominal segments strongly swollen and club-like, distinctly broader than previous ( +Fig. 285 +); tergum VII slender; +Cayman +Brac.............. + +woodruffi + + +n. sp. + + + + + + +3. Alae scarcely shorter than tegmina and covering roughly ½ of median segment, anal region reticulate; no white markings on pronotum and median segment;.......................................................................... 4 + + + +- Alae considerably shorter than tegmina and covering only 1/3 of metanotum, anal region red; lateral margins of pronotum white; median segment with a longitudinal white marking; +Bahamas +; Florida Keys; Dry +Tortugas +, +Navassa Island +, +Cayman Islands +& Swan Islands......................................................................... + +scabricollis + + + + + + + +4. Abdominal tergum VII slightly expanded posteriorly ( +Fig. 210 +); dorsal carinae of meso- and metafemora smooth; vomer with base large and terminal hook only about 1.2x longer than basal portion ( +Fig. 350 +).................... + +brachypterus + + +n. sp. + + + + + +- Abdominal tergum VII with a distinct triangular posterolateral lobe ( +Fig. 217 +); dorsal carinae of meso- and metafemora with a low triangular tooth sub-apically; vomer with base fairly small and the terminal hook papillate and almost +2x +longer than basal portion ( +Fig. 351 +)....................................................................... + +intermedius + + +n. sp. + + + + + + + +5. Head with cheeks white ( +Figs. 231–233 +); alae reaching to abdominal segment VI; +anterior +of pronotum with a distinct pair of spines ( +Figs. 231–233 +)........................................................................ + +micropterus + + + + + +- Head uniformly green (sometimes with a faint yellow marking on frons, +Fig. 194 +); alae at best reaching half way along abdominal segment V; +anterior +of pronotum merely with a pair of small tubercles ( +Fig. 194 +)....................... + +bicuspidatus + + + + + + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D34AFFF4FF27E871266919F0.xml b/data/38/7F/30/387F3068D34AFFF4FF27E871266919F0.xml new file mode 100644 index 00000000000..0d3ee25d031 --- /dev/null +++ b/data/38/7F/30/387F3068D34AFFF4FF27E871266919F0.xml @@ -0,0 +1,590 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Haplopus bicuspidatus +de Haan, 1842 + + + + + +( +Figs. 190–201 +, +338 +, +357 +, +380 +) + + + + + +Haplopus bicuspidatus +de Haan, 1842: 128 + +. +HT +, ♀:?; RMNH Leiden, +TYPE +, + +Haplopus bicuspidatum +de Haan, 1842 + +[RMNH]. Westwood, 1859: 87. + +Kirby, 1904a: 364. + +Redtenbacher, 1908: 433. [Suggesting possible synonymy with + +H. ligius +Westwood, 1859 + +] Otte & Brock, 2005: 150. + + + +Aplopus bicuspidatus +, Bragg, 1996: 109 + +. + +Bragg, 2001: 706. + + +Aplopus + +sp., Adams & Adams, 1982: 263. + +Gange, 1990: 18. [Culture report] +Kirby, 1904a: 364 (in part). +Redtenbacher, 1908: 432 (in part). +Moxey, 1972: 114 (in litt.; in part). + + + +Further material [2 +♂♂, +9 +♀♀, +eggs]: + + +HISPANIOLA ( +DOMINICAN REPUBLIC +): + + +1 ♀: +Dominican Republic +, Proyecto Biologico «La Huronera» La Victoria, Distrito Nacional, +IX.1992 +, Kelvin A. Guerrero, +NHMUK +(E) +2005-98 +[ +NHMUK +]; 1 ♀: Santo +Domingo +, +Dominican Republic +1925; G. Russo coll; +ANSP +; +USNM +; w0139; + +Diapherodes spinipes +Gray + +det. C.F. Moxey 1972 [ +USNM +]; 1 ♀: Santo +Domingo +, +Dominican Republic +1925; G. Russo coll; +USNM +; w0140; + +Aplopus ligius +Westw. + +♀ Topotype, A.n.c.; + +Diapherodes spinipes +Gray + +det. C.F. Moxey 1972 [ +USNM +]; +1 ♂ +, 2 ♀♀: ex Zucht: F. Hennemann, urspr.: +Dominikanische Republik +, 1993, PSG No. 48 [coll. FH, No. 0342- 1 to 3]; +1 ♂ +, 4 ♀♀, eggs: ex Zucht: F. Hennemann, urspr.: +Dominikanische Republik +, +VI.1995 +, PSG No. 48 [coll. FH, No. 0342-4 to 8 & ED]. + + + + +Diagnosis: +Very similar and presumably the sister-taxon of + +H. brachypterus + + +n. sp. + +. Females differ by: the larger size of both sexes; slight posterolateral lobe of abdominal tergum VII; alae which are longer than the tegmina (shorter in + +brachypterus + +); deeper posteromedian incision of the anal segment and larger and more acutely triangular epiproct ( +Fig. 197 +). Males differ from those of + +H. brachypterus + + +n. sp. + +by: the fully developed alae (37.0–41.0 mm); almost entirely green head ( +Fig. 194 +); obsolete +anterior +tubercles of the pronotum ( +Fig. 194 +); more decidedly excavated anal segment ( +Fig. 199 +) and shorter terminal hook of the vomer ( +Fig. 349 +). + + +From + +H. micropterus +(St. Fargeau & Audinet-Serville, 1838) + +it is easily distinguished by: the more elongate and slender body and less distinct +anterior +pair of tubercles on the pronotum of both sexes; smaller and acutely triangular supraanal plate of ♀♀ ( +Fig. 197 +), as well as the entirely green head ( +Fig 194 +); ochraceous antennae (orange to red in + +micropterus + +) and shorter alae of ♂♂, which merely reach to the +anterior +margin of abdominal segment V (reaching to tergum VI in + +micropterus + +). The eggs clearly differ from those of + +H. micropterus + +by the more elongate and more decidedly sculptured capsule and roundly convex to irregularly conical operculum ( +Figs. 200–201 +). + + + + + +Description: ♀ ( +Figs. 190–191 +). + +Of moderate size (body length including the subgenital plate 134.0– +153.5 mm +) but slender for the genus with a rather weakly developed thoracic armature. Colour ranging from drab over pale to dark brown, sometimes with a reddish or greenish wash. Abdomen to a variable degree furnished with paler and darker mottling and speckles. Head with the cheeks irregularly whitish and an elongate black marking running from the upper portion of the eyes towards the occipital horns; occasionally a further pair of black spots on the frons between the bases of the antennae. Antennae pale to mid brown. Spines of the thorax either brown or very dull green. Tegmina and costal region of alae mid to dark brown, rarely with a greenish wash; the latter blackish basally. Anal region of alae transparent with all major longitudinal and transverse veins broadly marked by dark brown bands. + + +Head: About 1.2x longer than wide, globose. Vertex rounded and with a pair of prominent but variably sized cephalad spines; these usually with a pointed tip ( +Fig. 193 +). Eyes circular and contained almost +3x +in length of cheeks. Antennae ± reaching half way along median segment and consisting of 54–56 segments. Scapus almost +2x +longer than wide and slightly narrowed towards the base. Pedicellus about half the length of scapus and distinctly shorter than III. + + +Thorax: Pronotum a little longer but slightly narrower than head, about 1.5x longer than wide, roughly rectangular but the lateral margins with a deep ± semi-circular median emargination. Transverse median sulcus deep, strongly curved but not reaching lateral margins of segment. Dorsal surface with a pair of low spiniform tubercles in the +anterior +portion, otherwise unarmed ( +Fig. 193 +). Prosternum and profurcasternum smooth. Mesothorax 2.5–2.6x longer than head and pronotum combined. Mesonotum rather narrow anteriorly and very slightly widened in median portion which is about as wide as posterior margin; surface with a variable number of spiniform tubercles or low spines; a rather defined marginal row of evenly sized tubercles is present laterally. Meso- and metapleurae with an irregularly longitudinal marginal row of spiniform tubercles. Meso- and metasternum sparsely granulose. Metanotum about ¼ the length of mesonotum, unarmed. Tegmina oval, coriaceous, with the venation very distinct, dense and irregularly disposed, and slightly projecting over posterior margin of metanotum; median protuberance very shallow. Alae longer than tegmina and reaching 2/3 to ¾ the way along median segment. + + + +FIGURES 190–192. + +Haplopus bicuspidatus +de Haan, 1842 + +. +160. +HT ♀: locality unknown [RMNH]; +191. +♀: captive reared from Dominican Republic [coll. FH, No. 0342-2]; +192. +♂: captive reared from Dominican Republic [coll. FH, No. 0342-1]. + + + +Abdomen: Median segment +2x +longer than wide and slightly narrowed medially. All segments unarmed. Segments II–V of roughly equal length, VI a little shorter than V, VII just a little more than ¾ the length of V; on average +2x +longer than wide. VII with lateral margins very slightly expanded posteriorly ( +Fig. 196 +). Praeopercular organ formed by a rough V-shaped swelling and two slight semicircular expansions at posterior margin of sternum VII ( +Fig. 338 +). VIII slightly shorter than VII, gently narrowed medially and almost 2.5x longer than wide. IX rectangular, slightly longer than wide and roughly half the length of VIII. Anal segment with a slight longitudinal carina which becomes gradually more decided towards the posterior, narrowed in posterior half and with a small triangular posteromedian indentation. Epiproct very small and acutely triangular ( +Fig. 197 +). Cerci very small, conical with a fairly acute tip and slightly laterally compressed; hardly projecting over posterior margin of anal segment. Subgenital plate very long, lanceolate, longitudinally carinate and with a ± acute apex; extending greatly over apex of abdomen ( +Figs. 195–196 +). + + + +FIGURES 193–201. + +Haplopus bicuspidatus +de Haan, 1842 + +. +193. +♀ head and pronotum: captive reared from Dominican Republic [coll. FH, No. 0342-5]; +194. +♂ head and pronotum: captive reared from Dominican Republic [coll. FH, No. 0342-8]; +195. +♀ apex of abdomen (lateral view); +196. +♀ apex of abdomen (dorsal view); +197. +♀ anal segment and epiproct (dorsal view); +198. +♂ apex of abdomen (lateral view); +199. +♂ apex of abdomen (dorsal view); +200. +Egg:captive reared from Dominican Republic (dorsal view) [coll. FH, No. 0342-E]; +201. +Egg captive reared from Dominican Republic (lateral view) [coll. FH, No. 0342-E]. + + +Legs: Profemora ¾ the length of mesothorax, mesofemora reaching about ¾ the way along abdominal segment II and metafemora almost reaching posterior margin of abdominal segment IV. Profemora occasionally with 1–3 minute spines in the apical half of the medioventral carina. Anteroventral carina of meso- and metafemora with two, posteroventral carina with only one sub-apical spine; medioventral carina armed with four distinct spines. Basitarsi about as long as following three tarsomeres combined. + + +♂ ( +Fig. 192 +). + +Of moderate size (body length 97.0–98.0 mm) and rather slender for the genus with well developed alae (length 37.0–41.0 mm). Colouration fairly complex with head and great parts of mesometapleurae, ventral body surface and legs green. Head plain green with the frons slightly yellowish ( +Fig. 194 +). Dorsal surface of thorax creamish mid brown, and drab to pale brown in abdomen. Spines of thorax with black tips. Meso- and metapleurae each with a pale brown longitudinal band along lower margin. Lateral margins of abdominal tergites VIII and IX broadly white. Tegmina and costal region of alae pale to mid brown, the latter with a few irregularly disposed pale markings along +anterior +margin and black basally. Basal portion of posterior margin of tegmina broadly white. Anal region of alae pink with all major veins brown. Antennae drab to ochraceous. Tarsi pale brown. + + +Head: Generally as in ♀♀ but with the cephald horns more slender and acute (Fig, 194). Eyes more prominent, projecting hemispherically and their length contained less than +2x +in that of cheeks. Antennae very robust and ± reaching posterior margin of abdominal segment III; with> 50 segments (broken in all specimens at hand). + + +Thorax: Pronotum slightly longer but narrower than head, general shape as in ♀♀; surface smooth except for a faint pair of low tubercles in the +anterior +portion ( +Fig. 194 +). Mesothorax about 2.3x longer than head and pronotum combined. Mesonotum with 4–8 small but pointed, rather irregularly disposed spines in the +anterior +2/3. Mesosternum and metasternum with a few irregularly disposed granules to low spiniform tubercles. Tegmina oval and slightly projecting over posterior margin of metanotum, central protuberance rather distinct and roundly conical. Alae slightly projecting over posterior margin of abdominal segment IV. + + +Abdomen: Segments II–IV of equal length and about 3.5x longer than wide. V–VII gradually decreasing in length with VII no more than 2.3x longer than wide. All tergites and sternites smooth. VII ± expanded posteriorly ( +Fig. 199 +). VIII shorter than VII and gently widening towards the posterior; IX ¾ the length of VIII and constricted medially. Anal segment with a faint longitudinal median carina which becomes gradually more decided towards the apex. Posterior portion strongly narrowed and laterally emarginated, the posterior margin with a distinct concave emargination medially ( +Fig. 199 +), slightly swollen and on ventral surface armed with several small, black incurving denticles. Epiproct small and with a posteromedian notch. Vomer with a large, roundly triangular base and a moderately long, up-curving terminal hook, which is about equal in length to basal portion ( +Fig. 357 +). Cerci large, obtuse, about equal in length to anal segment and slightly laterally compressed basally. Poculum moderately convex, cup-like and with a prominent, conical basal hump ( +Fig. 198 +); the posterior portion carinate longitudinally ( +Fig. 357 +). + +Legs: Pro- and mesofemora a little longer than mesothorax, metafemora projecting over posterior margin of abdominal segment IV. All legs less carinate than in ♀♀ but armature generally alike. Tarsi relatively more elongate and basitarsi a little longer than following three tarsomeres combined. + + +Egg ( +Figs. 200–201 +): + +Rather large for the genus, capsule elongate ovoid and 1.8x longer than wide; dorsal surface more convex than ventral surface. Capsule surface strongly coriaceous and irregularly granulose. Micropylar plate almost 3/5 the length of capsule and generally shaped like a bold inverted “Y”; the +anterior +half narrow and roughly parallel-sided, the posterior portion strongly diverging. Posterior margin with a wide and deep triangular emargination. Micropylar cup small and wart-like. Operculum ± round in cross-section, irregularly conically raised and strongly tuberculate. Colouration of capsule variable, ranging from pale drab over ochre to grey and to a variable degree furnished with weakly defined, dark brown to black markings. Capitulum pale drab to grey. + +Measurements [mm]: Length 3.9–4.4, length (including operculum) 4.1–4.7, width 2.2–2.3, heigth 2.4–2.7, length of micropylar plate 2.0–2.1. + +Variability: +This species shows much less intraspecific variability than e.g. + +H. micropterus +(St. Fargeau & Audinet-Serville, 1838) + +or + +H. scabricollis +(Gray, 1835) + +. In addition to the size and colouration the only features that underlie some variation in ♀♀ are the length of the subgenital plate, number and size of the mesothoracic tubercles and size of the cephalad horns. No considerable variation is seen in the two ♂♂ at hand, except for one having eight and the other one only four spines on the mesonotum. One specimen only has two or three spines on the medioventral carina of the mesofemora. + + + + +Comments: +This species was originally described from a single ♀ in RMNH and just briefly recognized by subsequent authors (e.g. Westwood, 1859 and Redtenbacher, 1908). Examination of the +holotype +and comparison with captive reared specimens originating in +the Dominican +Republic has shown these to be conspecific. The captive reared specimens include the so far unknown ♂♂ and eggs. Since only one additional wild-caught specimen is recorded here and none are represented in the extensive material from +the Dominican +Republic at hand + +H. bicuspidatus + +appears to be apparently rare. + + +Culture stock of + +H. bicuspidatus + +collected in +the Dominican +Republic was imported to Europe in the early 1980's (Adams & Adams, 1982) and included on the Phasmid Study Group culture-list as culture No. 48 “ + +Aplopus + +sp.” (later corrected to + +Haplopus cytherea + +). In captivity it readily accepts rose ( + +Rosa + +spp., +Rosaceae +), bramble ( + +Rubus fruticosus + +, +Rosaceae +), raspberry ( + +Rubus idaeus + +, +Rosaceae +), oak ( + +Quercus robur + +& + +Q. petraea + +, +Fagaceae +), guava ( + +Psidium guajava + +, +Myrtaceae +), eucalyptus ( + +Eucalyptus gunnii + +, +Myrtaceae +) and hawthorn ( + +Pyracantha + +spp., +Rosaceae +) as alternative food plants. + + + + + +Distribution ( +Fig. 380 +): + +Hispaniola ( +Dominican Republic +: Distrito Nacional) [NHMUK, USNM]. +Number of specimens examined: +12 + + + +TABLE 20. +Measurements of + +Haplopus bicuspidatus +de Haan, 1842 + +[mm] + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
♀, HT [RMNH]♀♀ [coll. FH)]♂♂ [coll. FH]♀ [MNHU]♂ [MNHU]
Body (incl. sg. pl.) Body140.5 125.0134.0–153.5 122.5–131.5- 97.0–98.0- 134.5- 105.0
Pronotum Mesonotum5.1 30.45.1–5.3 24.7–27.63.7–3.9 19.8–19.95.3 30.04.0 20.7
Metanotum Median segment6.9 9.27.0–7.5 8.5–9.16.8 7.97.0 8.9- -
Tegmina Alae10.2 11.38.2–10.2 9.6–12.910.0–11.2 37.0–41.010.0 12.010.8 44.5
Profemora Mesofemora21.8 19.919.5–23.0 17.2–19.821.8–22.2 21.4–25.223.2 19.823.5 21.0
Metafemora26.322.8–25.124.0–25.825.527.0
Protibiae Mesotibiae Metatibiae22.8 20.2 27.819.8–23.1 17.8–20.0 23.2–27.522.2–23.0 19.1–19.6 25.023.9 20.0 26.524.5 21.3 26.5
Antennae-46.0–50.0> 53.0> 45.573.0
+
+* a captive reared ♀ in coll. FH is unusually small, measuring only 116.0 mm (including the subgenital plate) and hence excluded from the table above. +
+
+
\ No newline at end of file diff --git a/data/38/7F/30/387F3068D351FFF0FF27EB4726071C29.xml b/data/38/7F/30/387F3068D351FFF0FF27EB4726071C29.xml new file mode 100644 index 00000000000..728af593a37 --- /dev/null +++ b/data/38/7F/30/387F3068D351FFF0FF27EB4726071C29.xml @@ -0,0 +1,418 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Haplopus brachypterus + +n. sp. + + + + +( +Figs. 193–210 +, +339 +, +358 +, +380 +) + + + + +HT, +♂: +Dominican Republic +, RD-248 Entrance to Sabana Iglesia, Santiago Prov., +372 m +, +19°20.196’N +70°45.483’W +, +29.IV.2004 +, DPerez, BHierro, R. Bastardo. (d) [USNM]. + + +PT, +1 ♀, +1 ♂ +: +Dominican Republic +, RD-248 Entrance to Sabana Iglesia, Santiago Prov., +372 m +, +19°20.196’N +70°45.483’W +, +29.IV.2004 +, DPerez, BHierro, R. Bastardo. (d) [USNM]. + + +PT, +2 ♂♂: +Dominican Republic +, Janico, Santiago Prov., +30.IX.1996 +, on + +Pictetia spinifolia +(Tabacuelo) + +, D. Perez, S. Navarro [USNM]. + + +PT, +1 ♀, +1 ♂ +(penultimate instar), 1 ♀ (nymph n4): +Dominican Republic +, RD-247 Rd. Inoa—El Caimito, nr. San Josè de las Matas, Santiago Prov., +552 m +, +19°22.225’N +71°00.661’W +, +28.IV.2004 +, D. Perez, BHierro, RBastardo (d/n) [USNM]. + + +PT, +1 ♀: Dominikaner +Republik Haiti +; Santiago de los Caballeros, P. Thumb leg., Eing. Nr. 92/37; PHA 7, Zoologisches Museum Hamburg [ZMUH]. + + +PT, +1 ♀: Dominikaner +Republik Haiti +; Santiago de los Caballeros, P. Thumb leg., Eing. Nr. 92/37; PHA 8, Zoologisches Museum Hamburg [ZMUH]. + + +PT, +1 ♀: Dominikaner +Republik Haiti +; Santiago de los Caballeros, P. Thumb leg., Eing. Nr. 92/37; PHA 9, Zoologisches Museum Hamburg [ZMUH]. + + +PT, +1 ♀: Dominikaner +Republik Haiti +; Santiago de los Caballeros, P. Thumb leg., Eing. Nr. 92/37; PHA 10, Zoologisches Museum Hamburg [ZMUH]. + + +PT, 3 +♂♂: Dominikaner-Republik +Haiti +, +Oktober 1936 +, Santiago de los Caballeros, P. Thumb leg., Eing. Nr. 92, 1937 [ZMUH—in alcohol]. + + + + +FIGURES 202–210. + +Haplopus brachypterus + +n. sp.. +202. +♀ PT: Dominican Republic, Santiago Province [USNM]; +203. +♂ HT: Dominican Republic, Santiago Province [USNM]; +204. +Head and pronotum of ♀ PT [USNM]; +205. +Head and pronotum of ♂ HT [USNM]; +206. +Tegmina and alae of ♂ PT [USNM]; +207. +Apex of abdomen of ♀ PT (lateral view) [USNM]; +208. +Anal segment and epiproct of ♀ PT (dorsal view) [USNM]; +209. +Apex of abdomen of ♂ HT (lateral view) [USNM]; +210. +Apex of abdomen of ♂ HT (dorsal view) [USNM]. + + + + +Diagnosis: +Very similar to + +H. bicuspidatus +de Haan, 1842 + +and + +H. intermedius + + +n. sp. + +. From the first it differs by: the slightly smaller dimensions of both sexes; presence of posterior tubercles on the pronotum; tuberculose profurcasternum; parallel-sided abdominal tergum VII; more shallow posteromedian excavation of the anal segment and smaller, transverse epiproct of ♀♀ ( +Fig. 208 +), as well as the conspicuously shortened alae (5.6–6.0 mm); distinct yellow markings on the frons and posterior portion of the cheeks ( +Fig. 205 +); more prominent and spiniform +anterior +spines of the pronotum ( +Fig. 205 +); less decidedly excavated anal segment ( +Fig. 208 +) and longer papillate terminal hook of the vomer of ♂♂ ( +Fig. 350 +). From + +H. intermedius + + +n. sp. + +, with which ♂♂ share the shortened alae, it can be distinguished by: the conspicuously less distinct posterolateral lobe of abdominal tergum VII and lack of a sub-apical tooth on the dorsal carinae of the meso- and metafemora of both sexes. ♀♀ also differ by: the slightly smaller dimensions; considerably smaller cephalad horns ( +Fig. 204 +); relatively longer mesothorax; absence of distinct paired posterior spines on abdominal tergites II–IV; absence of a sub-basal and sub-apical elevation of the anterodorsal carina of the meso- and metatibiae, and smaller epiproct ( +Fig. 208 +). Males have the anal region of the alae smaller and less well developed than in + +H. intermedius + + +n. sp. + +( +Fig. 206 +) and the cerci round in cross-section (compressed basally and carinate dorsally in + +intermedius + +). + + +The short alae of ♂♂ also resemble + +H. scabricollis +(Gray, 1835) + +from +the Bahamas +, Florida Keys, +Navassa Island +and +Cayman Islands +. They however clearly differ from ♂♂ of + +H.scabricollis + +by: the more slender body; lack of longitudinal white stripes along the lateral margins of the pronotum, and white median markings on the median segment and abdominal tergites VIII–X; convex and prominently bi-cornute vertex ( +Fig. 205 +); more decidedly excavated anal segment ( +Fig. 210 +) and more distinct central spine of the poculum ( +Fig. 209 +). Females are well distinguished from + +H. scabricollis + +by: the globose and prominently bi-cornute vertex ( +Fig. 204 +); longer alae; less decidedly tuberculose pronotum and smaller epiproct ( +Fig. 208 +). + + + + +Etymology: +The name “ + +brachypterus + +” refers to the conspicuously shortened alae of both sexes. + + + + + +Description: ♀ ( +Fig. 202 +). + +Of moderate size (body length including the subgenital plate 131.0–139.0 mm) and slender for the genus; body surface slightly glabrous. Colour creamish mid to dark brown with abdomen to a variable degree furnished with paler and darker mottling and speckles. Head with the cheeks irregularly whitish and a black marking above the eyes; two further small black spots on the frons between the bases of the antennae. Antennae dark ochraceous with a very slight reddish wash ventrally. Spines of the thorax dark reddish brown. +Anterior +portion of metapleurae whitish. Tegmina and costal region of alae dark brown to black with the veinature sepia; the latter blackish basally. Anal region of alae transparent and all major longitudinal and transverse veins broadly marked with dark brown. + + +Head: About 1.2x longer than wide, globose with the cheeks rather convex. Vertex rounded and with a pair of moderately sized and apically pointed cephalad spines ( +Fig. 204 +). Eyes circular and contained about +3x +in length of cheeks. Antennae ± reaching half way along median segment and consisting of about 64 segments. Scapus 2.2x longer than wide and gently expanded pre-apically. Pedicellus less than half the length of scapus and about equal to III. + + +Thorax: Pronotum a little longer but distinctly narrower than head, about 1.4x longer than wide, roughly rectangular but the lateral margins with a wide ± semi-circular emargination pre-medially. Transverse median sulcus deep, strongly curved but not reaching lateral margins of segment. Dorsal surface with a pair of low spines in the +anterior +portion and two pairs of small tubercles in the posterior portion (the posterior pair may be lacking, +Fig. 204 +). Prosternum smooth. Profurcasternum with three pairs of tubercles; a distinct pair marking the anterolateral angles of the segment, a much smaller pair at the posterior angles and a further even smaller pair posterior of distinct +anterior +tubercles. Mesothorax about 2.8x longer than head and pronotum combined. Mesonotum fairly narrow anteriorly but otherwise almost parallel-sided; surface with a variable number of spiniform tubercles or low spines; a rather defined marginal row of evenly sized tubercles is present laterally. Meso- and metapleurae with an irregular longitudinal marginal row of short but acute spines. Mesosternum sparsely set with some very low, irregularly paired spines, metasternum usually with two pairs of tubercles. Metanotum about ¼ length of mesonotum, unarmed. Tegmina oval, coriaceous, with the venation very distinct, dense and irregularly disposed, and slightly projecting over posterior margin of metanotum; median protuberance very shallow and slightly displaced towards the apex of tegmen. Alae very indistinctly longer than tegmina and reaching about ¾ the length along median segment. + + +Abdomen: Median segment +2x +longer than wide and very gently narrowed medially. All segments unarmed, except for a pair of very shallow tubercles near posterior margin of tergum II. Segments II–IV very slightly increasing in length, V as long as IV; the latter two segments about +2x +longer than wide. VI a little shorter and narrower than V, almost 2.5x longer than wide. Tergum VII slightly shorter than VI and parallel-sided, the posterolateral angles very slightly rounded; dorsal surface with two short converging carinae in posterior half. Praeopercular organ formed by an acute, longitudinal ridge in posterior portion of sternum VII ( +Fig. 339 +). Tergum VIII slightly shorter than VII, gently narrowed medially and almost 2.5x longer than wide. IX rectangular and about 2/3 the length of VIII. Anal segment with a very faint longitudinal median carina, narrowed in posterior half and with a shallow posteromedian emargination. Epiproct very small, roughly triangular and the projecting part wider than long ( +Fig. 208 +). Cerci very small, conical with a rather acute apex and slightly compressed laterally; hardly projecting over posterior margin of anal segment. Subgenital plate very long, lanceolate, longitudinally carinate and with a ± acute apex; extending greatly over apex of abdomen ( +Fig. 207 +). + +Legs: Profemora about 2/3 the length of mesothorax, mesofemora reaching about 1/3 the way along abdominal segment II and metafemora reaching about half way along abdominal segment IV. Profemora occasionally with 1–3 very minute spines in the apical half of the medioventral carina. Anteroventral carina of meso- and metafemora with two, posteroventral carina with one sub-apical spine; medioventral carina armed with four distinct spines. Basitarsi about as long as following three tarsomeres combined. + + +♂ ( +Fig. 203 +). + +Of moderate size (body length +83.2–87.5 mm +) and rather slender for the genus with conspicuously shortened alae (length +5.4–5.9 mm +). Colouration rather complex with great parts of head, mesometapleurae, ventral body surface and legs bright green. Head green with the frons yellow and a yellow postocular stripe along cheeks ( +Fig. 205 +). Dorsal surface of thorax creamish mid brown, of abdomen drab to pale brown. Pronotum yellowish laterally. Dorsal spines of pro- and mesothorax dark reddish brown with black points. Meso- and metapleurae with a washed longitudinal yellow marking in posterior portion and each with a dull yellow longitudinal band along lower margin. Lateral margins of abdominal tergites VIII and IX broadly white. Tegmina and costal region of alae mid to dark greyish brown; +anterior +margin and basal portion of posterior margin of tegmina, as well as +anterior +margin of alae broadly white; base of alae blackish. Anal region of alae pink with all major veins brown ( +Fig. 206 +). Antennae drab to ochraceous. Tarsi pale to mid reddish brown. + + +Head: Generally as in ♀♀ but with the cephalad horns more prominent, slender and acutely pointed ( +Fig. 205 +). Eyes more prominent, projecting hemispherically and their length contained only about +2x +in that of cheeks. Antennae moderately robust; broken in all specimens at hand. + + +Thorax: Pronotum slightly longer but narrower than head, general shape as in ♀♀; surface smooth except for a moderate pair of blunt spines or spiniform tubercles in the +anterior +portion ( +Fig. 205 +). Mesothorax about 2.5x longer than head and pronotum combined. Mesonotum with 7–8 pointed, irregularly dispersed but paired spines in the +anterior +2/3. Mesosternum and metasternum with several irregularly dispersed ± spiniform tubercles. Tegmina oval and ± reaching posterior margin of metanotum, central protuberance very shallow. Alae small, slightly shorter than alae and reaching only about 2/3 the way along median segment ( +Fig. 206 +). + + +Abdomen: Segment II a little shorter than III–IV and equal in length to V, about 2.7x longer than wide. III and IV longest segments and almost 3.5x longer than wide. V–VII gradually decreasing in length with VII no more than 2.3x longer than wide. All tergites and sternites smooth. VII slightly expanded posteriorly ( +Fig. 210 +). VIII shorter than VII and gently widening towards the posterior; IX about ¾ the length of VIII and narrowed towards the posterior. Anal segment with a faint longitudinal median carina which becomes gradually more decided towards the base. Posterior portion narrowed and laterally emarginated, the posterior margin with a shallow median emargination ( +Fig. 210 +), slightly swollen and on ventral surface armed with several small, black in-curving denticles. Epiproct very small ( +Fig. 210 +). Vomer with a rather small, roughly semi-circular base and a very long, papillate, up-curving terminal hook which is>1.5x longer than the basal portion ( +Fig. 358 +). Cerci large, obtuse and about equal in length to anal segment, very slightly laterally compressed basally. Poculum moderately convex, cuplike and with a prominent, acute and spiniform basal hump ( +Fig. 209 +); posterior portion carinate longitudinally ( +Fig. 358 +). + +Legs: Pro- and mesofemora very slightly shorter than mesothorax, metafemora projecting a little over posterior margin of abdominal segment IV. All legs less carinate than in ♀♀ but armature generally alike. Tarsi relatively more elongate and basitarsi a little longer than following three tarsomeres combined. + +Nymphs: +The half-grown ♀ and penultimate instar ♂ nymph at hand are greyish dark brown with fine pale grey mottling and both lack the sub-apical dorsal lobe on the meso- and metafemora, which distinguish them from nymphs of the very similar + +H. intermedius + + +n. sp. + +. The ♀ nymph has abdominal tergum VII with a distinct, rounded posterolateral lobe, hence has this much better developed than adult specimens. + + + + +Comments: +This new species appears to be not uncommon in the northwestern +Dominican Republic +and is known to feed on “Palo de Tabaco” ( + +Pictetia spinifolia + +, +Fabaceae +) at Janico. Eggs unknown. + +Distribution ( +Fig. 380 +): + +Hispaniola, NW-Dominican Republic (Santiago Province) [USNM, ZMUH]. +Number of specimens examined: +15 + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D355FFF3FF27EB4426091BF3.xml b/data/38/7F/30/387F3068D355FFF3FF27EB4426091BF3.xml new file mode 100644 index 00000000000..2eb4c24faa4 --- /dev/null +++ b/data/38/7F/30/387F3068D355FFF3FF27EB4426091BF3.xml @@ -0,0 +1,376 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + +Haplopus intermedius + +n. sp. + + +(Figs. 211–219, 359, 380) + + + +HT, +♂: +Dominican Republic +, RD-158, ~ +2 km +N Maizal, Valverde Prov., dry forest, +19°39.819’N +70°58.422’W +, +23.VII.2003 +, D. Perez, R. Bastardo, B. Hierro. (day) [ +USNM +]. + + +PT, +♀: +Dominican Republic +, RD-088 +4 km +E Montecristi, Montecristi Prov., +19°49.657’N +71°37254’W, +10.XII.2002 +, D. Perez, R. Bastardo (night) [ +USNM +]. + + +PT, +♂ (nymph n5): +Dominican Republic +, RD-088 +4 km +E Montecristi, Montecristi Prov., +19°49.657’N +71°37254’W, +10.XII.2002 +, D. Perez, R. Bastardo (night) [ +USNM +]. + + +PT, +♂ (nymph n4): +Dominican Republic +, RD-028 +5.II.02 +, +3 km +S. Montecristi, near road, Montecristi Prov., near sea level.Day. RB, BH, DP [ +USNM +]. + + + + +Diagnosis: +Very similar to + +H. bicuspidatus +de Haan, 1842 + +and + +H. brachypterus + + +n. sp. + +but well distinguished from both species by the triangular sub-apical tooth on the dorsal carinae of the meso- and metafemora of both sexes, as well as the sub-basal and sub-apical elevation of the anterodorsal carina of the meso- and metatibiae of ♀♀ and basally compressed and dorsally carinate cerci of ♂♂. From the first species ♀♀ also differ by: the presence of posterior tubercles on the pronotum and tubercles on the profurcasternum; slightly shorter mesothorax; considerably larger epiproct ( +Fig. 215 +) and distinct paired posterior spines on abdominal tergites II–IV ( +Fig. 218 +). Males readily differ from those of + +H. bicuspidatus + +by the shortened alae (length +5.6 mm +) and the posterolateral tooth or lobe of abdominal tergum VII ( +Fig. 217 +). From + +H. brachypterus + + +n. sp. + +this species can be distinguished by: the distinct posterolateral lobe of abdominal tergum VII and sub-apical tooth on the dorsal carinae of the meso- and metafemora of both sexes. Females furthermore differ by: the slightly larger dimensions; larger horns of the vertex; relatively shorter mesothorax; presence of a sub-basal and sub-apical elevation of the anterodorsal carina of the meso- and metatibiae, and larger epiproct ( +Fig. 215 +). Males have the anal region of the alae larger and better developed than those of + +H. brachypterus + + +n. sp. + +. + + +The short alae of ♂♂ also resemble + +H. scabricollis +(Gray, 1835) + +from +the Bahamas +, Florida Keys, +Navassa Island +and the +Cayman Islands +. They however clearly differ from ♂♂ of + +H. scabricollis + +by: the more slender body; lack of longitudinal white stripes along the lateral margins of the pronotum and white median markings on the median segment and abdominal tergites VIII–X; convex and prominently bi-cornute vertex; more decidedly excavated anal segment ( +Fig. 217 +) and more acute central spine of the poculum ( +Fig. 216 +). ♀♀ are well distinguished by: the globose and prominently bi-cornute vertex, longer alae and typical armature of the mid and hind legs. + + + + +Etymology: +The specific name “ + +intermedius + +” (lat. = inbetween) is meant to refer to the close relation to the genus + +Cephaloplopus + + +n. gen. + +in several morphological aspects. + + + + + +Description: ♀ ( +Fig. 211 +). + +Rather large (body length including the subgenital plate 152.0 mm) and slender for the genus; body surface slightly glabrous. Metathorax and great parts of abdomen discoloured to very dark brown during the process of dehydration in the unique ♀ +paratype +. Colour creamish mid brown and all over furnished with pale cream to whitish mottling and speckles. Head with lateral surfaces whitish and two small black markings above the eyes; vertex with irregular bown markings. Antennae mid grey dorsally, brown ventrally. Eyes dark reddish brown. Spines of the thorax dark sepia with the points black. Tegmina and costal region of alae dark brown with the venations of a slightly paler colour; the latter black basally. Anal region of alae transparent drab and all major longitudinal and transverse veins broadly marked with dark brown ( +Fig. 219 +). Legs and subgenital almost entirely creamish white with faint grey mottling. + +Head: About 1.2x longer than wide, globose with the cheeks fairly convex. Vertex rounded and armed with a pair of large apically pointed cephalad horns. Eyes circular and contained almost 3.5x in length of cheeks. Antennae broken in the only specimen available. Scapus 2.2x longer than wide with the lateral margins gently rounded. Pedicellus less than half the length of scapus and a little shorter than antennomere III. Both antennae broken in the only specimen available. + +Thorax: Pronotum longer but considerably narrower than head, almost +2x +longer than wide, roughly rectangular and with the lateral margins gently emarginated medially. Transverse median sulcus deep, almost straight and not reaching lateral margins of segment. Dorsal surface with a pair of moderately sized but pointed spines in the +anterior +portion; in posterior portion with two pairs of smaller spines. Prosternum smooth. Profurcasternum with three pairs of small tubercles, one pair marking the anterolateral angles of the segment, a much smaller pair at the posterior angles and a further even smaller pair positioned posterior of the distinct +anterior +tubercles. Mesothorax about 2.7x longer than head and pronotum combined. Mesonotum almost parallel-sided, the surface with a good number of irregularly disposed spines of variable size; along lateral margins with a marginal row of about eight small but pointed spines. Meso- and metapleurae armed with an irregular longitudinal marginal row of moderately sized spines. Mesosternum with four pairs of low spines, metasternum with two pairs of blunt spines. Metanotum about ¼ the length of mesonotum, unarmed. Tegmina oval, coriaceous, with the venation very distinct, dense and irregularly disposed; slightly projecting over posterior margin of metanotum. The median protuberance very shallow and conspicuously displaced towards the apex of tegmen. Alae a little longer than tegmina and reaching about 2/3 the way along median segment. + + +Abdomen: Median segment +2x +longer than wide and very gently narrowed medially. All segments unarmed, except for a pair of compressed posteromedian spines on tergites II–IV; this pair of spines most prominent on II ( +Fig. 218 +). Segments II–IV very slightly increasing in length, V as long as IV; the latter two segments about 1.8x longer than wide. VI a little shorter and narrower than V, about +2x +longer than wide. Tergum VII slightly shorter than VI and parallel-sided, with the posterolateral angles protuded into a rather narrow, blunt triangular lobe ( +Fig. 214 +). VIII slightly shorter than VII, gently narrowed medially and roughly 2.5x longer than wide. IX rectangular and slightly more than half the length of VIII. Anal segment with a very faint longitudinal median carina, narrowed in posterior half and with a deep triangular posteromedian emargination. Epiproct prominent, acutely triangular and projecting considerably over apex of anal segment ( +Fig. 215 +). Cerci small, conical with a rather acute tip and slightly compressed laterally; somewhat projecting over posterior margin of anal segment. Subgenital plate very long, lanceolate, carinate longitudinally and with a fairly acute apex; extending over apex of abdomen by more than the combined length of tergites VIII–X ( +Figs. 213–214 +). + + + +FIGURES 211–219. + +Haplopus intermedius + +n. sp.. +211. +♀ PT: Dominican Republic, Montecristi Province, nr. Montecristi [USNM]; +212. +♂ HT: Dominican Republic, Valverde Province, nr. Maizal [USNM]; +213. +Apex of abdomen of ♀ PT (lateral view) [USNM]; +214. +Apex of abdomen of ♀ PT (dorsal view) [USNM]; +215. +Anal segment and epiproct of ♀ PT (dorsal view) [USNM]; +216. +Apex of abdomen of ♂ HT (lateral view) [USNM]; +217. +Apex of abdomen of ♂ HT (dorsal view) [USNM]; +218. +Abdominal tergites II and II of ♀ PT showing the paired spiniform posterior projections (dorsal view) [USNM]; +219. +Right ala of ♀ PT [USNM]. + + +Legs: Profemora about 3/5 the length of mesothorax, mesofemora slightly projecting over median segment and metafemora reaching about 2/3 the way along abdominal segment IV. Profemora occasionally with three very minute spines in the apical half of the medioventral carina, otherwise unarmed. Anteroventral carina of meso- and metafemora with two, posteroventral carina with one sub-apical spine; medioventral carina armed with four prominent and strong spines. Both dorsal carinae with a triangular lobe-like tooth sub-apically. Anterodorsal carina of meso- and metatibiae with roundly triangular elevation sub-basally and sub-apically. Basitarsi about as long as following three tarsomeres combined. + + +♂ ( +Fig. 212 +): + +Of moderate size (body length +82.5 mm +) and rather slender for the genus with conspicuously shortened alae (length +5.6 mm +). Great parts of head, meso- metapleurae, ventral body surface and legs mid green. Head green with a faint yellow marking on the frons and a fine yellow postocular stripe. Dorsal surface of thorax and abdomen creamish mid brown. Dorsal spines of pro- and mesothorax mid brown with black points. Meso- and metapleurae with a very faint longitudinal yellowish marking in posterior portion and each with a dull orange longitudinal stripe along lower margin. Lateral margins of abdominal tergites VIII and IX broadly white. Tegmina and costal region of alae greyish mid brown and becoming darker towards the base; +anterior +margin and basal portion of posterior margin of tegmina, as well as +anterior +margin of alae broadly white; base of alae black. Anal region of alae pink with all major veins brown. Antennae greyish mid brown. Tarsi mid brown. + + +Head: Generally as in ♀♀ but eyes more prominent, projecting hemispherically and their length contained only about +2x +in that of cheeks. Antennae moderately robust and reaching to abdominal segment VI; with 61 segments. + + +Thorax: Pronotum slightly longer but narrower than head, general shape as in ♀♀ but relatively shorter and +anterior +margin slightly broader than posterior margin; surface smooth except for a moderate pair of spines in the +anterior +portion. Mesothorax about 2.7x longer than head and pronotum combined. Mesonotum in the HT with four paired spines at +anterior +margin and five further pointed spines in the median portion. Mesosternum with seven and metasternum with two pairs of spiniform tubercles. Tegmina oval and very slightly projecting over posterior margin of metanotum, central protuberance very shallow. Alae small, a little shorter than alae and hardly reaching 2/3 the way along median segment; anal region well developed. + + +Abdomen: Segments II a little shorter than III–IV and equal in length to V, about 3.2x longer than wide. III and IV longest segments and almost +4x +longer than wide. V–VII gradually decreasing in length with VII no more than 2.2x longer than wide. All tergites and sternites smooth. VII with a distinct, roundly triangular posterolateral tooth ( +Fig. 187 +). VIII slightly shorter than VII and very gently widening towards the posterior; IX about ¾ the length of VIII and narrowed towards the posterior. Anal segment with a very indistinct longitudinal median carina in basal portion and posterior margin with a distinct triangular median emargination ( +Fig. 217 +), slightly swollen and on ventral surface armed with several small, black in-curving denticles. Epiproct very small and roughly triangular ( +Fig. 217 +). Vomer with a broad, roughly semi-circular base and a very long, papillate, up-curving terminal hook ( +Fig. 359 +). Cerci large and about equal in length to anal segment; distinctly laterally compressed in basal portion and slightly longitudinally carinate dorsally ( +Figs. 187 +& +306 +). Poculum moderately convex, cup-like and with a conical basal hump ( +Fig. 216 +); posterior portion with a distinct longitudinal median keel. + +Legs: Pro- and mesofemora about 2/3 the length of mesothorax, metafemora projecting a little over posterior margin of abdominal segment IV. All legs less carinate than in ♀♀ but armature generally alike, except for the dorsal sub-apical teeth of the meso- and metafemora less distinct and dorsal elevations of the meso- and metatibiae lacking. Tarsi relatively more elongate and basitarsi a little longer than following three tarsomeres combined. + +Nymphs: +The two half-grown ♂ nymphs at hand are of a greyish brown colour with pale mottling and already show the characteristic features that distinguish this new species from + +H. brachypterus + + +n. sp. + +, having the sub-apical tooth on the dorsal carinae of the meso- and metafemora and the posterolateral lobe of abdominal tergum VII well developed. + + + + +Comments: +This pretty new species emphasizes the close relation between + +Haplopus +Burmeister, 1838 + +and + +Cephaloplopus + + +n. gen. + +by ♂♂ having basally compressed and slightly carinate cerci ( +Figs. 217 +, +351 +), a character otherwise unusual for + +Haplopus + +. Eggs unknown. + + + + + +Distribution ( +Fig. 380 +): + +Hispaniola, NW-Dominican Republic (Valverde Prov. & Montecristi Prov.) [USNM]. + + + + +Number of specimens examined: +4 + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D359FF01FF27EA3C26151E5A.xml b/data/38/7F/30/387F3068D359FF01FF27EA3C26151E5A.xml new file mode 100644 index 00000000000..9cb60455ae9 --- /dev/null +++ b/data/38/7F/30/387F3068D359FF01FF27EA3C26151E5A.xml @@ -0,0 +1,2273 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + +Aplopus micropterus +, Gray, 1835: 34 + +. + + + +Rehn, 1903: 136. +Wolcott, 1923: 23. +Wolcott, 1936: 35. +Wolcott, 1951: 50. + + +Diapherodes micropterus +, Moxey, 1972: 107 + +(in litt.; in part). + + + +Haplopus micropterus +, Westwood, 1859: 87 + +. + +Kirby, 1904a: 363. +Redtenbacher, 1908: 431. +Otte & Brock, 2005: 152. + + +Phasma (Haplopus) micropterum +, de Haan, 1842: 128 + +. + + + +Phasma angulata +Palisot de Beauvois, 1805: 166 + +, pl. 14: 4 (♀). +HT +, ♀: St. +Domingo +[presumed lost]. [ +Junior homonym +of + +Mantis angulata +Fabricius, 1793 + +] + + + +Phasma angulata +Stoll, 1813: 61 + +, pl. 21: 77 (♀). +HT +, ♀: St. Thomas [RMNH]. [ +Junior homonym +of + +Mantis angulata +Fabricius, 1793 + +] + + + +Haplopus angulatus +, Burmeister, 1838: 577 + +. + + + +Haplopus bituberculatum +de Haan, 1842: 128 + +. +HT +, ♀: + +Bituberculatum +de Haan + +,?; RMNH Leiden; +TYPE +, + +Haplopus bituberculatum +de Haan 1842 + +; RMNH +Holotype +[RMNH]. +n. syn. +Kirby, 1904a: 364. + +Redtenbacher, 1908: 433. + + +Aplopus bituberculatus +, Bragg, 1996: 109 + +. + +Bragg, 2001: 706. + + +Haplopus bituberculatus +, Otte & Brock, 2005: 151 + +. + + + +Haplopus cytherea +Westwood, 1859: 86 + +, pl. 18: 5, 5a & b (♂). +LT +, ♂ (by present designation): St. Dom.; E Coll ( +1870-73 +) W. W. Saunders, Purchased and pres. ’73 by Mrs. F. W. Hope; +Type +♂– Westwood, + +Haplopus cythereus +Westw., Cat. Phasm. 1859 + +, p. 86, pl. +18 f. +5; +Type +Orth: 617, + +Haplopus cythereus +Westw., Hope Dept. Oxford + +; + +Haplopus cythereus +Westwood + +, +Lectotype +, det. Brock, 1996 [OXUM, No. 617]; +PLT +, ♂: St. Dom.; + +Cytherea + +W.; +Type +♂—Westwood, + +Haplopus cythereus +Westw., Cat. Phasm. 1859 + +, p. 86, pl. +18 f. +5; +Type +Orth: 617, + +Haplopus cythereus +Westw., Hope Dept. Oxford + +; + +Haplopus cythereus +Westwood + +; +Paralectotype +, det. Brock, 1996 [OXUM, No. 617]. +n. syn. + +Kirby, 1904a: 363. + +Moxey, 1972: 114 (in litt.). [Listed as a synonym of + +Diapherodes spinipes +Gray, 1835 + +] + + + +Haplopus cythereus +, Redtenbacher, 1908: 432 + +. + +Otte & Brock, 2005: 151. + + +Aplopus cytherea +, Rehn, 1904: 63 + +. [Description of ♂] + + + +Haplopus ligia +Westwood, 1859: 89 + +, pl. 11: 1, 1a, 1b (♂) & 2, 2a (♀). +LT +, ♂ (by present designation): St. Dom. 55.1, + +Haplopus ligia +Westw. + +pl. 11 fig. 1, Westw. ♂, + +Haplopus ligia +Westwood + +, ST [NHMUK]; +PLT +, ♂: St. Dom. 55.1 [NHMUK]; +PLT +, ♀: St. Dom. 55.1, + +Haplopus Ligia +Westw. (St. +Domingo +) + +[NHMUK]; +PLT +, ♀: St. Dom. 55.1, + +Haplopus ligia +Westw. + +pl. 11 fig. 2, Westw. ♀, + +Haplopus ligia +Westwood + +, ST [NHMUK]. +n. syn. +Brock +et al. +, (in press) + +Kirby, 1904a: 364. +Redtenbacher, 1908: 432. +Moxey, 1972: 114 (in litt.). +Otte & Brock, 2005: 151. + + +Haplopus ligiolus +Redtenbacher, 1908: 432 + +. +LT +, ♂ (by present designation): 104; +Insel +Mona, zw. +Haiti +u. +Porto Rico +, W. Bock leg. ded. +12.IX.1892 +; PHA 22, Zoologisches Museum Hamburg [ZMUH]; +PLT +, ♀: 105; Ins. Mona b. +Hayti +, C. Bock leg. ded. +16.V. +184; cf. Stoll Taf. 21 fig. 17 Spectre à ailes petiter; PHA 26, Zoologisches Museum Hamburg [ZMUH]; +PLT +, ♀: 106; 10; Ins. Mona b. +Hayti +, C. Bock leg. ded +16.V.1894 +; PHA 27, Zoologisches Museum Hamburg [ZMUH]; +PLT +, ♀: “Westindien” [NHMB, No. VI.D.18]. +n. syn. + +Werner, 1929: 7, fig. A (♂). + +Moxey, 1972: 107 (in litt.). [Listed as a synonym of + +H. micropterus +(St. Fargeau & Audinet-Serville, 1825) + +] Hennemann & Conle, 1999: 11. + +Otte & Brock, 2005: 151. + + +Haplopus obtusus +Redtenbacher, 1908: 431 + +, pl. 19: 5 (♀). +HT +, ♀: Coll. Br. v. W., ex. coll. Sommer, Sta. Kruz, det. Br. v. W., + +Haplopus obtusus + +, 7646, 7646, + +P. angulata +Fabr. + +, + +P. gigas +Drury, Sta. Crux + +[NHMW, No. 835]. +n. syn. +Moxey, 1972: 107 (in litt.). [As a synonym of + +H. micropterus +(St. Fargeau & Audinet-Serville, 1825) + +] + + + +Aplopus obtusus +, Brock, 1998a: 47 + +. + + + +Haplopus obtusus +, Otte & Brock, 2005: 152 + +. + + + +Diapherodes spinipes +Gray, 1835: 34 + +. +HT +, ♀: no data [not traced—presumed lost]. [Replacement name for + +Phasma angulata +Palisot de Beauvois, 1805: 166 + +; not Fabricius, 1793, not Stoll, 1813] +n. syn. + + + +Diapherodes spinipes +, Moxey, 1972: 114 + +(in litt.). + + + +Haplopus spinipes +, Westwood, 1859: 87 + +. + +Kirby, 1904a: 363. +Redtenbacher, 1908: 431. +Otte & Brock, 2005: 152. + + +Aplopus + +sp., Wolcott, 1941: 40. + +Ramos, 1946: 9. +Wolcott, 1948: 50. +Wolcott, 1951: 50. + +[ +Not: + +Phasma angulata +Fabricius, 1793: 13 + +, = + +Diapherodes angulata angulata +(Fabricius, 1793) + +] + + +[ +Not: + +Phasma angulata +Fabricius, 1793: 13 + +, = + +Diapherodes angulata angulata +(Fabricius, 1793) + +] + + + +Further material [86 +♂♂, +111 +♀♀, +51 nymphs, eggs]: + + +VIRGIN ISLANDS +(ST. CROIX): + + +1 ♀: Annaly St. Croix, Virgin Is., on grass in field, +Oct. 15,59 +, C.-W. Miskimen, 60 4291; USMNH; w0195; + +Diapherodes micropterus +(St. F. & Serv.) + +det. C.F. Moxey 1972 [USNM]. + + +VIRGIN ISLANDS +(ST. THOMAS): + + +1 ♀: 806; + +micropterus +Gray, Westw. + +*, +Cyphocr. + +microptera +Serv. + +, + +angulata +, St. Thomas, Moritz + +[MNHU]; 1 ♀: St. Thomas, W.- +Ind +., C. Calwood leg., ded. +28.XII.1895 +; PHA 25, Zoologisches Museum Hamburg [ZMUH]. + + +VIRGIN ISLANDS +( +ST. JOHN +): + + +1 ♀, 1 ♀ (penultimate instar): +St. John +[MNHU]. + + +PUERTO RICO +: + + +1 ♂ +: Guánica, P.R., +2.Oct.1937 +, W. García; USMNH; w0199 [USNM]; 1 ♀: Rincon, P.R., +Nov. 1938 +, Coll. S.R. Sada; USMNH; w0196; + +Diapherodes micropterus +(St. F. & Serv.) + +det. C.F. Moxey 1972 [USNM]; 2 ♀♀, 5 ♂♂, eggs: ex Zucht F. Hennemann, Herkunft: +Puerto Rico +, +VI.1995 +[coll. FH, No’s 0243-20 to 26 & E3]. + + +MONA +ISLAND +: + + +1 ♂ +: Mona +Island +, Aug 10.1938, Coll. A. Palmer; USMNH; w0198; + +Diapherodes micropterus +(St. F. & Serv.) + +det. C.F. Moxey 1972 [USNM]. + + +HISPANIOLA ( +DOMINICAN REPUBLIC +): + + +2 ♂♂: +Dominican Republic +, +Isla +Beata, +27.VII.1977 +,? Eugenio Marcano, NHMUK(E) +2005-98 +, ex. Museo Nacional de Historia Natural Sto. +Domingo +[NHMUK]; +1 ♂ +: +Dominican Republic +, Cerretera Romana—Bayahibe, +19.IX.1994 +, Kelvin A. Guerrero, NHMUK(E) +2005-98 +[NHMUK]; +1 ♂ +: +Dominican Republic +, Punta Villa Mella, Distrito Nacional, +3.X.1993 +, Kelvin A. Guerrero, NHMUK(E) +2005-98 +[NHMUK]; 3 ♂♂, 2 ♀♀, +4 eggs +: +Dominican Republic +, RD-052 Pueblo Nuevo, Baní Peravia Prov., +27.VII.2002 +, 97 m ( +400 ft +.), +18°17.757’N +70°19.601’W +, D. Perez, R. Bastardo [USNM]; 3 ♂♂, 1 ♀, +1 ♂ +(nymph n4): +Dominican Republic +, RD-062 ~ +5 km +W Las Américas, Santo +Domingo +, +18°28.158’N +69°43.601’W +, +19.XI.2002 +, D. Perez, R. Bastardo, B. Hierro [USNM]; 2 ♂♂, 3 ♀♀, 2 ♀♀ (penultimate instar), 4 ♀♀ (nymph n4), 2 ♀♀ (nymphs n3), 1 ♀ (nymph n2), +1 ♂ +(penultimate inatar): +Dominican Republic +, RD-060 Monte Rio, ~ +70 m +, dry scrub, +18°22.972’N +70°43.036’W +, +17.XI.2002 +, D. Perez, R. Bastardo, B. Hierro. (night) [USNM]; 1 ♀: +Dominican Republic +, RD-091, Sierra Prieta, Santo +Domingo +Prov., +133 m +, +18°39.010’N +69°58.409’W +, +18.III.2003 +, D. Perez, R. Bastardo, B. Hierro (night) [USNM]; 2 ♂♂, 2 ♀♀, +1 egg +: +Dominican Republic +, RD-034 Boca de la +Cañada +, ~ +15 km +S Oviedo, Pedernales Prov., +4.VII.2002 +, +17°54.901’n +71°30.067’W +, B. Hierro, R. Bastardo, D. Perez [USNM]; 1 ♀, 1 ♀ (nymph n3), +7 eggs +: +Dominican Republic +, RD-153 La Poza de Agua Nueva, El Curro, Sierra Martín Garcia, Azua Prov., +18°18.324’N +70°57.176’W +, ~ +800 m +, +15–16.VII.2003 +, D. Perez, R. Bastardo, B. Hierro. (day/night) [USNM]; 1 ♀, +3 eggs +: +Dominican Republic +, RD-146 ~ +2 km +S Pinosdel Edén, Sierra de Neiba, Independencia Prov., +18°34.758’n +71°45.804’w +, +8.VII.2003 +, D. Perez, R. Bastardo, B. Hierro. (night) [USNM]; 1 ♀ (penultimate instar): +Dominican Republic +, RD-079 +Isla +Beata, trail to Cueva del Tubo, PNJ, +17°36.844’N +71°31.379’W +, +3.XII.2002 +, Dperez, Bhierro, Rbastardo. (day/night). [USNM]; 1 ♀ (nymph n5): +Dominican Republic +, +San Cristóbal +Prov., Sabana de Hatillo, on + +Malpighia gossipifolia + +(cerazas), +13.XII.1994 +, D. E. Perez [USNM]; +1 ♂ +(penultimate instar): +Dominican Republic +, RD-069 Km 54 Rd. Azua-Barahona, Barahona Prov., +70 m +, +18°21.871’N +71°09.080’W +, +24.XI +,2002, D. Perez, B. Hierro, H. Andújar. (night). [USNM]; +1 ♂ +(nymph n5): +Dominican Republic +, RD-156 La Furnia, Berreras, Azua Prov., +18°19.289’N +70°54.755’W +, +18.VII.2003 +, D. Perez, Rbastardo, Bhierro (n) [USNM]; 1 ♀ (n4): +Dominican Republic +, RD-063 Sierra Prieta, Santo +Domingo +Prov., +18°38.315’N +69°58.302’W +, +20.XI.2002 +, D. Perez, R. Bastardo, B. Hierro [USNM]; 1 ♀ (n4): +Dominican Republic +, RD- 0 25 +1–2.II.02 +km 10 on Rd. to Los + +Anones, Ocoa Prov., +1070 + +m, 347–605 mE 2052–511 mN. RB, BH, DP [USNM]; 1 ♀ (n3): +Dominican Republic +RD-210 Mirador del Hoyo de Pelempito, P. N. Sierra de Bahoruco, Pedernales Prov., +1.250 m +, +18°05.396’N +71°30.663’W +, +5.IV.2004 +, D. Perez, R. Bastardo, B. Hierro (d/n) [USNM]; +1 ♂ +: El Choco, Puerto Plata +2-IV- 2000 +en + +Bidens cynapiifolia +R. H. Bastardo + +[USNM]; 4 ♀♀: +Dominican Republic +, +200 m +N Puente Coronel Barahona Prov., +22.ix.2000 +D. Perez, R. Bastardo, B. Hierro [USNM]; 1 ♀: +Dominican Republic +, La Altagracia Prov., Bayahibe, 2001, D. E. Perez [USNM]; 1 ♀: +Dominican Republic +, RD-219 Sierra Prieta, Villa Mella, Santo +Domingo +Prov., +142 m +, +18º38.925’N +69º58.303’W +, +12.iv.2004 +, D. Perez, B. Hierro, R. Bastardo. (n) [USNM]; 2 ♂♂ (nymphs): +Dominican Republic +, RD-153 La Poza de Agua Nueva, El Curro, Sierra Martín García, Azua Prov., +18°18.324’N +70°57.176’W +, ~ +800 m +, +15–16.vii.2003 +, D. Perez, R. Bastardo, B. Hierro. (day/night) [USNM]; +1 ♂ +: +Dominican Republic +, Azua Prov., Rd. Monte Rio—Puerto Viejo, +18°23.570’N +70°42.758’W +, +120 m +, +15.viii.2006 +, D. Perez, R. Bastardo, B. Hierro, S. Medrano (night) [USNM]; +1 ♂ +, 1 ♀ (nymphs): +Dominican Republic +, RD-272 Caseta 1, P N Sierra de Bahoruco, Independencia prov., +18º16.038’N +71º32.691’W +, +1,239 m +, +14.vii.2004 +, D. Perez (d) [USNM]; +1 ♂ +: +Dominican Republic +, RD-276 Boca de Yuma, P N del Este, La Altagracia prov., +18º19.554’N +68º48.503’W +, near sea level, +19–20.vii.2004 +, D. Perez (d/n) [USNM]; +1 ♂ +: +Dominican Republic +, RD-092 Blanco (near hydroelectric), Bonao, Monseñor Nouel Prov., +18°52.946’N +70°30.337’W +, +19.iii.2003 +, D. Perez, R. Bastardo, B. Hierro. (night) [USNM]; +1 ♂ +: +Dominican Republic +, RD-103 Rd. to Majagual, Sierra de Neiba, Bahoruco Prov., +669 m +, +18°32.340’N +71°18.118’W +, +25.iii.2003 +, D. Perez, R. Bastardo, B. Hierro. (night) [USNM]; 1 ♀ (nymph): +Dominican Republic +, RD-069 km 54 Rd. Azua—Barahona, Barahona Prov., +70 m +, +18°21.871’N +71°09.080’W +, +24.xi.2002 +, D. Perez, B. Hierro, H. Andujar. (night) [USNM]; 3 ♂♂: +Dominican Republic +, RD-079 +Isla +Beata, on way to Cueva del Tubo, Parque Nacional Jaragua, nr. sea level, +17°36.844’N +71°31.379’W +, +3.xii.2002 +, D. Perez, B. Hierro, R. Bastardo. (night) [USNM]; +1 ♂ +(nymph): +Dominican Republic +, RD-182 Loma Quita Espuela, Firme de loma, S. F. de Macorís Prov., +19º21.101’N +70º08.930’W +, +715 m +, +3–4.xii.2003 +, D. Perez, R. Bastardo, A. Marmolejos (day/night) [USNM]; 1 ♀: +Dominican Republic +RD-171 El Maizal, near Presa de Valdesia, Peravia Prov., +18°22.942’N +70°16.859’W +, +97 m +, +31.vii.2003 +, D. Perez, R. Bastardo, B. Hierro. (day) [USNM]; 2 ♀♀: Dominican Republi,c RD-212 +150 m +N bridge on road Cabo Rojo—Aceitillar, Pedernales prov., +16 m +, +17º58.530’N +71º39.034’W +, +7.iv.2004 +, D. Perez, B. Hierro, R. Bastardo. (d/n) [USNM]; 2 ♂♂, 4 ♂♂ (nymphs), 1 ♀ (nymph): +Dominican Republic +, La Altagracia Prov., Bayahibe, +26/ix/1999 +(night) D. Perez, R. Bastardo, L. Ramos. [USNM]; +1 ♂ +(nymph): +Dominican Republic +, Jánico, Santiago Prov., +30 ix 1996 +, on + +Pictetia spinifolia +(Tabacuelo) D. Perez, S. Navarro + +[USNM]; +1 ♂ +(nymph): +Dominican Republic +, RD-182 Loma Quita Espuela, Firme de loma, S. F. de Macorís Prov., +19º21.101’N +70º08.930’W +, +715 m +, +3–4.xii.2003 +, D. Perez, R. Bastardo, A. Marmolejos (day/night) [USNM]; 2 ♂♂, 1 ♀: RD: La Altagracia Higüey Punta Cana +20–28-vii-2000 +R. Bastardo [USNM]; +1 ♂ +: +Dominican Republic +, RD-005 +15.i.02 +Las Yayitas, Azua Prov., +240 m +, 316–230 mE 2046–941 mN. D. Otte, D. Perez, R. Bastardo, S. Medrano [USNM]; +1 ♂ +: +Dominican Republic +, RD-056 Pueblo Nuevo, Baní, Peravia Prov., dry scrub, +18°17.672’N +70°19.922’W +, +16.xi.2002 +, D. Perez, R. Bastardo, B. Hierro. (night) [USNM]; 1 ♀: +Dominican Republic +, RD-027 +2.ii.02 +Km 7 on Rd. to Presa Jiguey, Ocoa Prov., +860 m +, 345–778 mE 2053–018 mN. Night collection. D. Perez, R. Bastardo, B. Hierro [USNM]; 1 ♀: +Dominican Republic +, RD-156 La Furnia, Barreras, Azua Prov., +18°19.289’N +70°54.755’W +, +18.vii.2003 +, D. Perez, R. Bastardo, B. Hierro. (night) [USNM]; 1 ♀ (nmyph): +Dominican Republic +, RD-062 ~ +5 km +W of Las Americas Airport, nr. LADOM, Santo +Domingo +Prov., +18°28.158’N +69°43.601’W +, +19.xi.2002 +, D. Perez, R. Bastardo, B. Hierro. (night) [USNM]; 3 ♀♀: +Dominican Republic +, RD-052 Pueblo Nuevo, Baní, Peravia Prov., +27.vii.2002 +, 97 m ( +400 ft +.), +18º17.757’N +70º19.601’W +, D. Perez, R. Bastardo [USNM]; +1 ♂ +: +Dominican Republic +, RD-016 +19.i.02 +Km 26 Rd. Cabo Rojo- Aceitillar, Pedernales Prov., +680 m +, 222–642 mE 2004–651 mN, transition forest. D. Otte, D. Perez, R. Bastardo, S. + + +Medrano, B. Hierro [USNM]; +1 ♂ +(nymph): +Dominican Republic +, RD-041 Sierra Prieta, Villa Mella, Santo +Domingo +Prov., +18º38.939’N +69º58.373’W +, + +8.vii. +2002 + +, 500 ft., +8.vii.2002 +. D. Perez, B. Hierro, R. Bastardo, S. Medrano. [USNM]; +1 ♂ +: +Dominican Republic +, RD-019 +22.i.02 +Talanquera, +San Pedro +de Macoris Prov., disturbed scrub forest, about +20 m +above sea level, +18º26.35’N +69º24.06’W +, D. Otte, D. Perez [USNM]; +1 ♂ +: +Dominican Republic +, RD-060 Monte Rio, +4 km +W of beach, ~ +70m +, dry scrub, +18°22.972’N +70°43.036’W +, +17.xi.2002 +, D. Perez, R. Bastardo, B. Hierro. (night) [USNM]; 2 ♀♀: +Dominican Republic +, RD-034 Boca de la +Cañada +, ~ +15 km +S Oviedo, Pedernales Prov., +4.vii.2002 +, +17º54.901’N +71º30.067’W +, B. Hierro, R. Bastardo, D. Perez. [USNM]; 4 ♂♂, 3 ♀♀: +Dominican Republic +, RD-199 Boca de Yuma, P. N. Del Este, La Altagracia Prov., +20 m +, +18º21.875’N +68º37.081’W +, +16–17.xii.2003 +, D. Perez, R. Bastardo (day/night). [USNM]; 2 ♂♂, 3 ♀♀: +Dominican Republic +, RD-055 ~ +2 km +N Bayahibe, La Altagracia Prov., +31.vii.2002 +, +18º23.423’N +68º50.453’W +, D. Perez, R. Bastardo, B. Hierro [USNM]; +1 ♂ +: +Dominican Republic +, RD-067 Laguna Grande, Las Lagunas, Padre Las Casas, Azua Prov., +18°48.088’N +70°52.842’W +, +23.xi.2002 +, +1,033 m +, D. Perez, B. Hierro, H. Andujar. (day) [USNM]; 4 ♂♂ (nymphs), 4 ♀♀ (nymphs): +Dominican Republic +, Pedernales, +Lado +Fundacipe, Pedernales Prov., +18°01.8’N +71°44.7’W +, +19–20 iii 1999 +, D. E. Perez, S. Navarro [USNM]; +1 ♂ +, 1 ♀, +1 ♂ +(nymph): +Dominican Republic +, Paraiso, Barahona Prov. +17°59.1’N +71°10’W +21 iii 1999 +D. Perez, S. Navarro [USNM]; +1 ♂ +: +Dominican Republic +, Punta Cana Beach Resort, Reserva Ecologica Punta Cana, La Altagracia Prov., +23/xii/2008 +D. E. Perez [USNM]; +1 ♂ +, 5 ♀♀, +1 ♂ +(nymph), 1 ♀ (nymph): +Dominican Republic +, +San Cristobal +Prov., Sabana de Hatillo, on + +Malpighia gossipifolia + +(cerezas), +25.ix.1996 +, D. E. Perez [USNM]; 2 ♂♂, 1 ♀, 1 ♀ (nymph): +Dominican Republic +, RD-195 ~ +6 km +S of Cabral, dry forest, Barahona Prov., +18º12.252’N +71º14.401’W +, +247 m +, +13.xii.2004 +, D. Perez, R. Bastardo, B. Hierro (night). [USNM]; +1 ♂ +, 5 ♀♀: +Dominican Republic +, RD-196 ~ +4 km +S of Cabral, Barahona Prov., +18º13.835’N +71º14.251’W +, +105 m +, +14.xii.2003 +, D. Perez, R. Bastardo, B. Hierro (night). [USNM]; 7 ♂♂, 5 ♀♀, 1 ♀ (nymph): +Dominican Republic +, RD-191 Around Caseta No. 1, Parque Nacional Sierra de Bahoruco, +1,239 m +, Independencia Prov., +18º16.038’N +71º32.691’W +, +11–12.xii.2003 +, D. Perez, R. Bastardo, B. Hierro. (day/night) [USNM]; +1 ♂ +: +Dominican Republic +, Prov. Barahona, +1 km +from Entrada to Vincente Noble, R.E. Woodruff, coll. +30-IV-78 +[FSCA]; 1 ♀: +Dominican Republic +, WI Baoruco Mts., +1250 m +, +11. Sept. 1973 +, Coll. #3, TJ Wakler, JC Schuster [FSCA]; 1 ♀: +Dominican Republic +, Pedernales Prov., N of Cabo Rojo, +18.IX.1973 +, JC Schuster [FSCA]; 2 ♂♂: +Dominican Republic +, Pr. Pedernales, Km +12 N. +Cabo Rojo, +21-vi-1999 +R. E. Woodruff, Prosopis at night [FSCA]; +1 ♂ +, +1 ♂ +(nymph): +Dominican Republic +, +15 km +N Cabo Rojo, +21.vi.1999 +R. E. Woodruff & R. M. Baranowski [FSCA]; +1 ♂ +: +Dominican Republic +, +Isla +Saona, +6.vii.2002 +C. Nuñez [MNHNSD]; 1 ♀: +Dominican Republic +, RD-063 Sierra Prieta, Santo +Domingo +Prov., +18°38.315’N +69°58.302’W +, +20.XI.2002 +, D. Perez, R. Bastardo, B. Hierro [MNHNSD]; 3 ♀♀, 2 ♂♂: +Dominican Republic +, RD-065 Monte Rio, ~ +4.5 km +W of beach, Azua Prov., dry scrub, +18°23.728’N +70°42.726’W +, +22.xi.2002 +, D. Perez, B. Hierro, H. Andujar. (night) [MNHNSD]; +1 ♂ +, 1 ♀: +Dominican Republic +, RD-078 El Cajuil, Oviedo, Pedernales Prov., +52 m +, +17°48.783’N +71°21.538’W +, +2.xii.2002 +, D. Perez, B. Hierro, R. Bastardo. (night) [MNHNSD]; 1 ♀, 1 ♀ (nymph): +Dominican Republic +, RD-083 Juan Dolio, +San Pedro +de Macorís Prov., sea level, nr. +18°26.35’N +69°24.06’W +, +6.xii.2002 +, D. Perez, R. Bastardo. (night) [MNHNSD]; +1 ♂ +, 1 ♀ (nymph): +Dominican Republic +, RD-084 ~ +10 km +S of Ocoa, nr. main road, Ocoa Prov., +468 m +, +18°28.350’N +70°29.670’W +, +7.xii.2002 +, D. Perez, R. Bastardo. (night) [MNHNSD]; 1 ♀: Rep. Dom., Prov. Santo +Domingo +, Distrito Nacional, San Juan Bosco #63, +16.VIII.2005 +, R. Gonzáles y M. Díaz [MNHNSD]; 1 ♀: Rep. Dom., Prov. Santo +Domingo +Este, Boca Chica, La Malena, +20.X.1979 +, Marcano y Domínguez [MNHNSD]; 1 ♀: Rep. Dom., Prov. +San Cristóbal +, Villa Altagrica, La Cumbre, +14.VI.2001 +, C. Núñez [MNHNSD]; 1 ♀ (penultimate instar): Rep. Dom., Prov. +San Cristóbal +, Los Desamparados, +24.VII.1981 +, H. Domínguez [MNHNSD]; +1 ♂ +: Rep. Dom., Prov Pedernales, Cabo Rojo, +10.I.1998 +, M. Hernández [MNHNSD]; +1 ♂ +: Rep. Dom., Prov. Santo +Domingo +Norte, Mirador Norte, +7.X.2001 +, H. Takizawa [MNHNSD]; +1 ♂ +: Rep. Dom., Prov. Santo +Domingo +Norte, Mirador Norte, +12.VIII.2001 +, H. Takizawa [MNHNSD]; +1 ♂ +(penultimate instar): Rep. Dom., Prov. +San Cristobal +, +Haina +, +23.VI.1981 +, H. Domínguez [MNHNSD]; +1 ♂ +: Rep. Dom., Prov. Azua, El Número, +4.VII.2002 +, H. Takizawa [MNHNSD]; +1 ♂ +(penultimate instar): Rep. Dom., +Isla +Saona, de Catuano a Damaney, +6.VII.2002 +, H. Takizawa [MNHNSD]; +1 ♂ +: G.V, P53, +23.VII.1992 +[MNHNSD]; 1 ♀: +República Dominicana +Prov. +San Cristóbal +, +11.II.1977 +E. Marcano; #21060 [IIBZ]; 1 ♀ (apex of abdomen missing): +República Dominicana +Prov. +San Cristóbal +, Cambita, +8.VI.1976 +, E. Marcano; #20069 [IIBZ]; 1 ♀ (apex of abdomen missing): +República Dominicana +Prov. +San Cristóbal +, Campus Loyola, +30.X.1975 +, E. Marcano; #19189 [IIBZ]; 1 ♀: +República Dominicana +Santo +Domingo +, Capital, +11.VI.1973 +E. Marcano; #13677[IIBZ]; 1 ♀: +República Dominicana +Prov. +San Cristóbal +, Campus Loyola, +30.X.1975 +, E. Marcano; #19190 [IIBZ]; 1 ♀: +República Dominicana +Prov. +San Cristóbal +, Politécnico Loyola, +VII.1989 +, E. Marcano [IIBZ]; 1 ♀: +República Dominicana +Prov. +San Cristóbal +, Cambita, +8.VI.1976 +, E. Marcano; #20070 [IIBZ]; 1 ♀: +República Dominicana +Prov. Santo +Domingo +, +8.XII.1964 +, E. Marcano; #909 [IIBZ]; 1 ♀: +República Dominicana +Prov. +San Cristóbal +, cuidad, +19.V.1976 +, E. Marcano; #20065 [IIBZ]; 1 ♀: +República Dominicana +Prov. Barahona, +1.VI.1967 +, E. Marcano & I. Fernández; #4212 [IIBZ]; 1 ♀: +República Dominicana +Prov. +San Cristóbal +, Campus Loyola, +30.X.1975 +, E. Marcano; #19187 [IIBZ]; 1 ♀: +República Dominicana +Santo +Domingo +, Distrito Nacional, Engombe, +19.VI.1979 +[IIBZ]; 1 ♀: +República Dominicana +Prov. +San Cristóbal +, ciudad, +10.IV.1975 +, E. Marcano; #17985 [IIBZ]; 1 ♀: +República Dominicana +Prov. +San Cristóbal +, ciudad, +19.V.1976 +, E. Marcano; #20064 [IIBZ]; +1 ♂ +: +República Dominicana +Prov. +San Cristóbal +, Campus Loyola, +23.X.1975 +, E. Marcano,; #19038 [IIBZ]; 1 ♀: +República Dominicana +Prov. +San Cristóbal +, Campus Loyola, +30.X.1975 +, E. Marcano; #19190 [IIBZ]; 1 ♀. +República Dominicana +Prov. +San Cristóbal +, Campus Loyola, +5.III.1976 +, E. Marcano; #19687 [IIBZ]; 1 ♀: +República Dominicana +Prov. +San Cristóbal +, +21.I.1975 +E. Marcano;#17497 [IIBZ]; 1 ♀: +República Dominicana +Prov. Barahona, +10.VI.1967 +, E. Marcano; #4196 [IIBZ]; 1 ♀: +República Dominicana +Prov. +San Cristóbal +, cuidad, +19.V.1976 +, E. Marcano; #20063 [IIBZ]; 1 ♀: +República Dominicana +Prov. Santo +Domingo +, +9.II.1969 +, E. Marcano,;#4854 [IIBZ]; 1 ♀: +República Dominicana +Prov. +San Cristóbal +, Campus Loyola, +30.X.1975 +, E. Marcano; #19188 [IIBZ]; 1 ♀: +República Dominicana +Prov. +San Cristóbal +, cuidad, +19.V.1976 +, E. Marcano; #20062 [IIBZ]; 1 ♀ (apex of abdomen missing): +República Dominicana +Prov. La Vega, Constanza, La Palma, +1.VIII.1968 +, E.Marcano & S. Raud; #4589 [IIBZ]; +1 ♂ +: +República Dominicana +, Santo +Domingo +, Distrito Nacional, octubre del 1970 [IIBZ]; 1 ♀: +República Dominicana +Prov. +San Cristóbal +, Campus Loyola, +6.I.1976 +, E. Marcano; #19549 [IIBZ]; 1 ♀ (apex of abdomen missing): +República Dominicana +Prov. +San Cristóbal +, Cambita, +8.VI.1976 +, E. Marcano; #20070 [IIBZ]; 1 ♀: +República Dominicana +Prov. +San Cristóbal +, Campus Loyola, +30.X.1975 +, E. Marcano; #19190 [IIBZ]; 1 ♀: +Dominican Republic +, Pedernales +30 km +N Cabo Rojo +1070 m +, 18-07N W71–39W +27 September 1991 +R. Davidson, C. Young, S. Thompson, J. Rawlins Reservoir, pine woods [CMNH]; +1 ♂ +: Republique Dominicaire, route Oviedo à Pedernales km 17, Jaragua National Park, +11-V-2004 +, J. Barlout réc. [MNHN]; +1 ♂ +: +République Dominicaine +, route Oviedo à Pedernales km17, Jasagua National Park, +11.V.2004 +, J. Barbut réc [MNHN]; 8 ♂♂, 4 ♀♀, eggs: ex Zucht: F. Hennemann, +VI.1995 +, Herkunft: Dominikanische Rep., PSG No. 61 [coll. FH, No’s 0243-1 to 12 & E1]; +1 ♂ +, 6 ♀♀: ex Zucht: F. Hennemann, +2001–2002 +, Herkunft: Dominikanische Rep., PSG No. 61 [coll. FH, No’s 0243-13 to 19 & E2]. + + +HISPANIOLA ( +HAITI +): + + +1 ♂ +: Furcy, +Haiti +, I.21.1945, Anthony Curtis!, wO134; + +Diapherodes spinipes +(Gray) + +det. C. F. Moxey [ANSP]; +1 ♂ +: Furcy, +Haiti +, I.21.1945, Anthony Curtis!, wO136; + +Diapherodes spinipes +(Gray) + +det. C. F. Moxey [ANSP]; 1 ♀: Furcy, +Haiti +, Feb. 5.1943, A. Curtis; wO138; + +Diapherodes spinipes +(Gray) + +det. C. F. Moxey [ANSP]; 1 ♀: Furcy, +Haiti +, Feb. 5.1943, A. Curtiss; wO139; + +Diapherodes spinipes +(Gray) + +det. C. F. Moxey [ANSP]; +1 ♂ +: +Haiti +, Dept. +De +l’Ouest, Port au Prince, +5.IX.1973 +, JC Schuster [FSCA]; 1 ♀: Coll. Br. v. W., Port au Prince, Stevens; det. Br. v. W. + +Haplopus ligia +Westw. + +; 72., 6479, 6479 [NHMW]; 1 ♀: Port au Prince, +Haiti +, Dr. Fritz Rauch leg., ded. +31.XII.1900 +; PHA 24, Zoologisches Museum Hamburg [ZMUH]; 1 ♀: Port au Prince, +Haiti +, Dr. Rauch leg., W. Pohlmann durch Gust. Keitel jr., ded. +29.V.1901 +; PHA 23, Zoologisches Museum Hamburg [ZMUH]. + +NO DATA: + +1 ♀: + +Aplopus ligius +Westw. A. + +n.c. [USNM]; +1 ♂ +: W. +Ind +.; + +Aplopus cythereus +Westw. + +♂ det. Rehn [USNM]. + + +Diagnosis: +This widely distributed and very variable species is readily distinguished from all other species in the genus by the large roundly triangular, shield-shaped or almost semi-circular epiproct of ♀♀ ( +Figs. 241–242 +), as well as the distinctly white cheeks ( +Figs. 231–233 +), orange to red antennae, short terminal hook of the vomer ( +Fig. 352 +) and long alae of ♂♂, which clearly project over posterior margin of abdominal segment V ( +Figs. 224–227 +). + + +Description: +The description of the colouration is mostly based on colour photographs of various live wild and captive reared specimens. + + + +♀ ( +Figs. 220–223 +, +386–387 +). + +Very variable in size (body length including the subgenital plate 115.5–172.0 mm) and several morphological features like the armature of the head and thorax, abdominal tergites, shape of the epiproct, and length of the subgenital plate and alae (→ comments on variability below). Colour ranging from dull green, over straw, grey and pale to dark brown, sometimes with a yellowish or reddish wash and with a variable degree of white portions in some localities. Abdomen in particular to a variable degree furnished with paler and darker mottling and speckles. Head with the cheeks ± distinctly white and one or two small black spots over the eyes; occasionally a further pair of black spots on the frons between the bases of the antennae. Antennae pale to mid brown dorsally and dull red ventrally. Spines of the thorax either brown, dull red or green. Tegmina and costal region of alae mid to dark brown, rarely with a greenish wash; either plain or to a variable degree furnished with faint pale brown or grey spots. Anal region of alae transparent with all major longitudinal and transverse veins broadly marked by dark brown ( +Fig. 248 +). + + +Head: About 1.3x longer than wide and roughly oval in dorsal aspect. Vertex rounded and with a pair of very prominent but variably sized occipital spines; points either blunt or with a pointed black tip ( +Figs. 228–230 +). Occasionally one or two further pairs of small spiniform tubercles close to posterior margin of head capsule ( +Fig. 230 +). Eyes circular and contained about 2.5x in length of cheeks. Antennae ± reaching to posterior margin of median segment and consisting of 60–66 segments. Scapus almost +2x +longer than wide and slightly narrowed towards the base. Pedicellus about half the length of scapus and roughly equal in length to III. + + +Thorax: Pronotum a little longer but slightly narrower than head, about 1.6x longer than wide, roughly rectangular but the lateral margins with a deep roundly triangular emargination medially. Transverse median sulcus moderately distinct and almost reaching lateral margins of segment. Dorsal surface at least with a distinct pair of spines +in anterior +portion, but usually with a very variable number of additional spines and tubercles ( +Figs. 228–230 +). Probasisternum and profurcasternum with single granules or tubercles. Mesothorax 2.0–2.3x longer than head and pronotum combined. Mesonotum rather narrow anteriorly and very slightly gradually widened towards the posterior; surface armed with a very variable number of differently sized tubercles or blunt spines, a rather defined marginal row of evenly sized tubercles or small spines is present laterally. Meso- and metapleurae with an irregular longitudinal marginal row of spiniform tubercles or spines. Meso- and metasternum with a variable number of granules or low spiniform tubercles; may be no more than four on the metasternum. Metanotum less than 1/3 the length of mesonotum, unarmed. Tegmina oval, coriaceous, with the venation very distinct, dense and irregularly disposed, and slightly projecting over posterior margin of metanotum; median protuberance rather faint and roundly conical. Alae variable in length but always longer than tegmina; at least reaching ¾ along median segment but often projecting to +anterior +portion of abdominal tergum II ( +Fig. 223 +). + + +Abdomen: Median segment +2x +longer than wide and slightly narrowed medially. Segments II–V of roughly equal length, VI a little shorter than V, VII just a little more than ¾ the length of V; on average 1.6–1.8x longer than wide. Tergites II–IV often with a median pair of tubercles or spiniform processes close to posterior margin; most prominent on II ( +Figs. 234–235 +). VII with four very fine and low, longitudinal, sub-parallel carinae and lateral margins ± deflexed posteriorly or with a ± acutely triangular posterior lobe ( +Figs. 237–239 +). Praeopercular organ formed by a slightly raised dark oval marking in posterior margin of sternum Vii, which bears a rough, rounded tubercle posteriorly ( +Fig. 340 +). Tergum VIII slightly shorter than VII, gently narrowed medially and almost 2.5x longer than wide; sometimes with a pair of posteromedian tubercles. IX rectangular and roughly half the length of VIII. Anal segment with a distinct longitudinal carina, narrowed in posterior half and with a widely triangular posteromedian emargination. Epiproct prominent and at least 1/3 the length of anal segment; size and shape variable but mostly ranging from roundly triangular to almost semicircular and shield-like ( +Figs. 241–242 +). Cerci conical with a rather acute tip and slightly laterally compressed, hardly projecting over posterior margin of anal segment. Subgenital plate very long, lanceolate or cymbiform, longitudinally carinate and with a ± acute apex; extending greatly over apex of abdomen ( +Figs. 236–240 +). + +Legs: Profemora shorter than mesothorax, mesofemora about as long as metathorax and metafemora reaching ± half way along abdominal segment IV. Profemora occasionally with one or two small sub-apical spines on the medioventral carina. Protibiae often gently undulate dorsally. Anteroventral carina of meso- and metafemora with two, posteroventral carina with only sub-apical spine. Medioventral carina of mesofemora with 3–5, of metafemora with 5–7 ± prominent spines. Dorsal carinae each with a ± distinct roundly triangular tooth or expansion; much more prominent on the posterior carina. Posteroventral carina of meso- and metatibiae very minutely denticulate; anterodorsal carina occasionally with a roundly triangular tooth some ¼ off the base. Basitarsi about as long as following three tarsomeres combined. + + +♂ ( +Figs. 224–227 +, +388 +). + +Variable in size (body length 82.6–103.0 mm) and colouration but well recognized by the ± white cheeks and long alae. Although some morphological features vary to a certain degree, the variation is much less than in ♀♀. Alae well developed (length 40.5–51.0 mm) and at least reaching to abdominal tergum VI. Great parts of meso- and metapleurae, ventral body surface and legs green. Head either green or pale brown with the cheeks ± distinctly white ( +Figs. 231–233 +). Dorsal surface of thorax and abdomen straw to pale creamish brown. Spines of thorax either dull green or black, posterior portions of meso- and metapleurae yellow and the metapleurae with a pale brown longitudinal band along lower margin. Lateral margins of abdominal tergum VIII and IX broadly white. Tegmina and costal region of alae pale to creamish mid brown and to a variable degree furnished with irregularly disposed pale cream to white markings; +anterior +margin of tegmina broadly white and basal portion of alae black. Anal region of alae pink with all major veins brown ( +Fig. 247 +). Antennae, except scapus and pedicellus, ± distinctly red. Tarsi greenish brown. In addition to this more common green form described above brown forms occur in certain localities ( +Fig. 227 +). These generally agree in colouration to the green forms but lack all the green body parts described above. + + +Head: Generally as in ♀♀ but with the cephalad horns often more prominent ( +Figs. 231–233 +). Eyes more prominent, projecting hemispherically and contained no more than 1.6x in length of cheeks. Antennae very robust and ± reaching posterior margin of abdominal segment III; with 60–66 segments. + + +Thorax: Pronotum longer but narrower than head, general shape as in ♀♀. Armature usually limited to a prominent pair of spines in the +anterior +portion but sometimes a much smaller pair of spines may be present in the posterior portion ( +Figs. 231–233 +). Mesothorax about 2.0–2.2x longer than head and pronotum combined. Mesonotum with 4–10 distinct and ± pointed, roughly paired spines in the +anterior +2/3 of the surface. Mesosternum with a few irregularly disposed granules or low spiniform tubercles; metasternum either smooth or with 2–4 paired tubercles +in anterior +portion. Tegmina oval and slightly projecting over posterior margin of metanotum, central protuberance roundly conical. Alae at least reaching 1/3 the way along abdominal segment VI. + + + +FIGURES 220–223. + +Haplopus micropterus +(St. Fargeau & Audinet-Serville, 1828) + +. +220. +HT ♀: St. Thomas [RMNH]; +221. +HT ♀ of synonym + +Haplopus obtusus +Redtenbacher, 1908 + +: St. Croix [NHMW, No. 835]; +222. +♀: Dominican Republic, Pedernales Province, Boca de la Cañada [USNM]; +223. +♀: Dominican Republic, Azua Province, El Curro (specimen with very long alae) [USNM]. + + + + +FIGURES 224–227. + +Haplopus micropterus +(St. Fargeau & Audinet-Serville, 1828) + +. +224. +♂: captive reared from Dominican Republic [coll. FH, No. 0243-19]; +225. +♂: Dominican Republic, Baní Peravia Province, Pueblo Nuevo [USNM]; +226. +♂: Dominican Republic, Monte Rio [USNM]; +227. +♂: Dominican Republic, Pedernales Province, Boca de la Cañada [USNM]. + + + +Abdomen: Segments II–IV of equal length and about 3.2x longer than wide. V–VII slightly decreasing in length with VII no more than 2.3x longer than wide. All tergites and sternites smooth. VII slightly expanded posteriorly or with a ± distinct triangular lobe ( +Figs. 244–245 +). VIII ¾ the length of VII and gently widening towards the posterior; IX shorter than VIII. Anal segment with a faint longitudinal median carina which gradually becomes more decided towards the apex. Posterior portion rounded and with a wide triangular median emargination ( +Figs. 244–246 +); posterior margin slightly swollen and on ventral surface armed with several small, black in-curving denticles ( +Fig. 360 +). Epiproct very small and roundly triangular ( +Fig. 246 +). Vomer broad with a large, rounded base and a fairly short terminal hook ( +Fig. 360 +). Cerci large, obtuse and almost as long as anal segment, slightly laterally compressed basally. Poculum moderately convex, cup-like and with a blunt basal hump ( +Fig. 243 +); posterior portion carinate longitudinally. + + + +FIGURES 228–235. + +Haplopus micropterus +(St. Fargeau & Audinet-Serville, 1828) + +. +228. +Head and pronotum of ♀ from Dominican Republic, Independencia Province, Sierra de Neiba [USNM]; +229. +Head and pronotum of ♀ from Dominican Republic, Pedernales Province, Boca de la Cañada [USNM]; +230. +Head and pronotum of ♀, captive reared from Dominican Republic [coll. FH, No. 0243-15]; +231. +Head and pronotum of ♂ from Dominican Republic, Baní Peravia Province, Pueblo Nuevo [USNM]; +232. +Head and pronotum of ♂ from Dominican Republic, Baní Peravia Province, Pueblo Nuevo [USNM]; +233. +Head and pronotum of ♂ from Dominican Republic, Santo Domingo Province, Santo Domingo [USNM]; +234. +Abdominal tergum II of ♀ from Dominican Republic, Pedernales Province, Boca de la Cañada [USNM]; +235. +Abdominal tergum II of ♀, captive reared from Dominican Republic [coll. FH, No. 0243-15]. + + + + +FIGURES 236–248. + +Haplopus micropterus +(St. Fargeau & Audinet-Serville, 1828) + +. +236. +Apex of abdomen of ♀ HT (lateral view) [RMNH]; +237. +Apex of abdomen of ♀ HT (dorsal view) [RMNH]; +238. +Apex of abdomen of ♀ from Dominican Republic, Pedernales Province, Boca de la Cañada (dorsal view) [USNM]; +239. +Apex of abdomen of ♀ PLT of synonym + +Haplopus ligius +Westwood, 1859 + +(dorsal view) [NHMUK]; +240. +Apex of abdomen of ♀ PLT of synonym + +Haplopus ligius +Westwood, 1859 + +(lateral view) [NHMUK]; +241. +Anal segment and epiproct of ♀ from Dominican Republic, Pedernales Province, Boca de la Cañada (dorsal view) [USNM]; +242. +Anal segment and epiproct of ♀, captive reared from Dominican Republic) (dorsal view) [USNM]; +243. +Apex of ♂ abdomen, captive reared from Dominican Republic (lateral view) [coll. FH, No. 0243-19]; +244. +Apex of ♂ abdomen captive reared from Dominican Republic (dorsal view) [coll. FH, No. 0243-19]; +245. +Apex of abdomen of ♂ LT of synonym + +Haplopus ligius +Westwood, 1859 + +(dorsal view) [NHMUK]; +246. +Anal segment of ♂, captive reared from Dominican Republic (dorsal view) [coll. FH, No. 0243-19]; +247. +Left ala of ♂, captive reared from Dominican Republic [coll. FH, No. 0243-19]; +248. +Left ala of ♀, captive reared from Dominican Republic [coll. FH, No. 0243- 13]. + + + + +FIGURES 249–256. + +Haplopus micropterus +(St. Fargeau & Audinet-Serville, 1828) + +, Eggs. +249. +Dominican Republic, Azua Province, El Curro (dorsal view) [USNM]; +250. +Dominican Republic, Azua Province, El Curro (lateral view) [USNM]; +251. +Captive reared from Dominican Republic (dorsal view) [coll. FH, No. 0243-E2]; +252. +Captive reared from Dominican Republic (lateral view) [coll. FH, No. 0243-E2]; +253. +Dominican Republic, Baní Peravia Province, Pueblo Nuevo (dorsal view) [USNM]; +254. +Dominican Republic, Baní Peravia Province, Pueblo Nuevo (lateral view) [USNM]; +255. +Captive reared from Puerto Rico (dorsal view) [coll. FH, 0243-E3]; +256. +Captive reared from Puerto Rico (lateral view) [coll. FH, 0243-E3]. + + +Legs: Profemora about as long as mesothorax, mesofemora slightly shorter than mesothorax and metafemora ± reaching to posterior margin of abdominal segment IV. Armature generally as in ♀♀ but less distinct and the meso- and metafemora lacking the sub-apical dorsal tooth or expansion seen in ♀♀. Tarsi relatively more elongate and basitarsi a little longer than following three tarsomeres combined. + +Nymphs: +Very variable in colour, size and shape of the armature of the head, thorax, abdomen and legs, which generally is much stronger developed than in adult insects. Colour various shades of brown, often with a greenish wash and/or all over furnished with whitish speckles and markings. + + + +Egg ( +Figs. 249–256 +): + +A large number of eggs were examined from various localities throughout +the Dominican +Republic, +Puerto Rico +and the +British Virgin Islands +. Just like the insects, these show considerable variability which however is mainly limited to the size and colouration. + + +Rather large for the genus, capsule ovoid and 1.5–1.7x longer than wide; dorsal surface more convex than ventral surface. Capsule surface ± coriaceous and granulose. Micropylar plate roughly 2/3 the length of capsule, narrowed +in anterior +portion, then gradually widened with the posterior portion broadly rounded. Posteromedially with a deep triangular to parallel-sided emargination. Micropylar cup small and cup-shaped. Operculum ± round in cross-section, convex and in centre with a large, squamiform, mushroom-shaped capitulum (height> +0.3 mm +). Colouration of capsule highly variable and ranging from pale drab over ochre and grey to dull orange brown; usually to a variable degree furnished with dark brown to black markings, spots and speckles. Capitulum dull yellow, straw or pale ochre. + +Measurements [mm]: Length 3.1–3.7, length (including operculum) 4.3–4.8, width 2.1–2.6, height 2.4–2.7, length of micropylar plate 2.3–2.5. + +Variability: +This is a very variable species which not only varies from locality to locality but also shows considerable variation within single colonies or culture-stocks reared in Europe. The most important variable characters are summarized separately for each sex below. + + +Numerous features underlie considerable variability in ♀♀, some of which have already been mentioned in the description presented above. The body length ranges from 114.0–172.0 mm including the subgenital plate (103.0– +152.5 mm +excluding it), with the largest specimens occuring on Hispaniola. The cephalad horns are variable in size and may either be blunt (most specimens from +Puerto Rico +& +Virgin Islands +) or have a conspicuous, acute black point at the apex (most Hispaniolan specimens). The pronotum may be covered with numerous paired tubercles but in some cases merely bears a single pair of spines in the +anterior +portion. The armature is particularly distinct and well developed in specimens from certain localities in +the Dominican +Republic (e.g. Boca de la +Cañada +, Pedernales Province or Sierra Martín García, Azua Province). The mesothoracic armature is extremely variable with structures ranging from small spiniform tubercles to prominent spines. Some captive reared specimens from Hispaniola in the first author's collection (coll FH, No's 0243-2 & 17) merely have the mesonotum with a few small irregularly dispersed tubercles, while there are numerous spines of variable sizes in some wild ♀♀ at hand from +the Dominican +Republic. The ♀ from near Cabo Rojo (Pedernales Province, +Dominican Republic +) in FSCA is very small (body length 103.0 mm and 114.0 mm including the subgenital plate) but has the mesothoracic armature extremely prominent and the mesonotum and metapleurae all over armed with medium to large conical spines. Abdominal tergites II–IV usually bear a median pair of tubercles or spiniform processes close to posterior margin, which vary strongly in size and are most prominent on II ( +Figs. 234–235 +). Often there are only processes on II and more rarely these are entirely lacking. The alae may just reach ¾ the way along the median segment but in extremes also cover the +anterior +portion of abdominal tergum II ( +Fig. 223 +). Depending on the locality, the antennae are just slightly reddish in most Hispaniolan specimens but distinctly dull red in specimens from +Puerto Rico +and the +Virgin Islands +. + + +Males are much less variable than ♀♀ with variability generally restricted to the size, colouration, size of the cephalad horns ( +Figs. 231–233 +), number of spines on the mesothorax and granules on the meso- and metasternum, shape of abdominal tergum VII as well as the number of spines on the medioventral carina of the femora. The latter shows the same range as in ♀♀. In addition to the features mentioned the pronotum may occasionally bear a further pair of spiniform tubercles in the posterior portion. They occur in a common green form ( +Figs. 224–226 +) and more rarely encountered brown form. The brown specimens found in certain localities in +the Dominican +Republic (e.g. Boca de la +Cañada +, Pedernales Province, +Fig. 227 +) fully agree with the green form except for lacking any of the green body parts. The ventral body surface, meso- and metapleurae and legs are all greyish mid brown with irregular whitish mottling. The spines of the thorax however are dull green and the brown ♂♂ from the mentioned locality at hand also have the basal portion of the posterior margin of the tegmina white. + + +Specimens at hand from Parque Nacional Sierra de Bahoruco (RD-191) in USNM deserve special mention. Females are considerably more stocky with the mesothorax relatively shorter and the armature much more prominently developed than in all other examined specimens. But despite the different appearance at first glance, the genital morphology of both sexes does not show any characters that would allow a clear distinction as a distinct subspecies or species. Only the epiproct of ♀♀ is on average larger than in other specimens but seems to be within the range of variability of + +H. micropterus + +. + + +As in the insects, considerable variability is also seen in the eggs which however mainly is mainly limited to the colouration as well as the size of the capitulum ( +Figs. 219–226 +). Eggs laid by specimens from +Puerto Rico +( +Figs. 225–226 +) or the +British Virgin Islands +appear to be generally more reddish and have less distinct mottling, while eggs at hand from localities throughout +the Dominican +Republic are often prettily mottled with dark brown ( +Figs. 219–222 +). However, remarkable variation is already seen within single colonies or culture-stocks and almost plain reddish brown eggs are also laid by some colonies in +the Dominican +Republic (e.g. from Pueblo Nuevo, Peravia Province). + + +Comments: +This species was first illustrated and described by Stoll (1788, pl. 21: 77) from a ♀ presumed from “ +Amboina +” and subsequently (Stoll, 1813) named + +Phasma angulata + +. The name “ + +Phasma angulata + +” had however already been used for another species by Fabricius in 1793 (→ + +Diapherodes angulata angulata +(Fabricius, 1793)) + +, and for this reason Saint Fargeau & Audinet-Serville (1828: 445) introduced + +Cyphocrana microptera + +as a replacement name for Stoll's species. There has been confusion concerning the published year of + +Haplopus micropterus +(St. Fargeau & Serville) + +but according to Sherborn & Woodward (1899: 595) it should be 1828, not 1825 as recorded previously. + + +The +holotype +of + +Phasma angulata +Stoll + +(= + +Cyphocrana microptera +St. Fargeau & Audinet-Serville, 1828 + +) was not traced in RMNH by Bragg (1996) and since believed lost. Certainly, no author had ever seen Stoll's +type +specimen but an extensive search in the collection of RMNH in 2006 has revealed a ♀ which perfectly matches with the illustration provided by Stoll (1788, pl. 21: 77) and is here regarded as the previously missing +holotype +. The particular specimen is pinned with the same typical insect pin used in all of Stoll's +types +in RMNH and furthermore bears the same typical circular label seen on most of Stoll's specimens. Based on Stoll's figure the main diagnostic character of this species in the past has been the presence of a conspicuous white spot in the basal portion of the alae, which is however not seen in any known representative of + +Haplopus + +. Examination of the ♀ +holotype +shows this to have a large hole in each wing caused by a pin drawn through the wing by the preparator to spread these organs, hence are an artifact. The size and shape of these holes correspond to the “white spots” reproduced in Stoll's illustration and prove this artifact to have been misinterpreted by all subsequent authors dealing with the systematics of + +H. micropterus + +. + + + +H. micropterus + +shows a great deal of intraspecific variability and is widely distributed throughout Hispaniola, Mona +Island +, +Puerto Rico +and the +Virgin Islands +. The variability of certain characters is summarized above and has caused much confusion in the identity of this species and also resulted in several synonymies. + + +Examination of the ♀ +holotype +of + +H. bituberculatum +de Haan, +1842 + +in RMNH leaves no doubt this species is a synonym of + +H. micropterus + +, which might even have been collected alongside with the HT specimen described and illustrated by Stoll ( +n. syn. +). It is pinned on the same kind of insect pin. Another synonym is represented by + +Haplopus obtusus +Redtenbacher, 1908 + +whose ♀ +holotype +from “Sta. Kruz” (= +Saint Croix +) is a typical specimen of + +H. micropterus + +( +n. syn. +). The short and apically rounded subgenital plate of the +holotype +has proven to be an artifact, the apex being broken off and swollen due to an injury. Redtenbacher (1908: 432) described + +Haplopus ligiolus + +based on a ♂ and two ♀♀ from Mona +Island +in ZMUH and a ♀ from “Westindien” in NHMB. Although all three specimens are traced, + +H. ligiolus + +was omitted in the catalogue of type-material deposited in ZMUH by Zompro (2002). The ♂ in ZMUH is here designated as the +lectotype +of + +H. ligiolus +Redtenbacher, +1908 + +in order to guarantee stability of the name and the synonymy here established. Careful examination of the four specimens has shown + +H. ligiolus + +to be a synonym of + +H. micropterus + +( +n. syn. +). + +Haplopus cytherea +Westwood, 1859 + +was described from two ♂♂ from Santo +Domingo +in OXUM of which one (the specimen illustrated by Westwood, 1859, pl. 18: 5) is here selected as the +lectotype +. Both are typical specimens of + +H. micropterus + +, and for this reason this species also becomes a synonym ( +n. syn. +). Examination of the type-specimens of + +Haplopus ligia +Westwood, +1859 + +in NHMUK has shown these to represent merely a variety of this very variable species, consequently also + +H. ligia + +is a junior synonym of + +H. micropterus + +( +n. syn. +). The Santo +Domingo +specimen illustrated by Palisot de Beauvois (1805: 166, pl. 14: 4) as + +Phasma angulata + +is, as already noted by Westwood (1859: 87), a ♀ with the last three abdominal segments broken off and is clearly distinct from the species that was described as + +Mantis angulata + +by Fabricius (1793: 13, = + +Diapherodes angulata angulata +(Fabricius) + +from +Guadeloupe +). Since Palisot de Beauvois's + +angulata + +is a junior homonym of + +Mantis angulata +Fabricius, 1793 + +, Gray (1835: 34) introduced + +Diapherodes spinipes + +as a replacement name for Palisot de Beauvois's species. The +holotype +of + +Phasma angulata +Palisot de Beauvois, 1805 + +(= + +spinipes +Gray, 1835 + +) is lost but the figure of Palisot de Beauvois leaves no doubt it is conspecific with + +H. micropterus + +, hence + +D. spinipes + +as well is a junior synonym ( +n. syn. +). + + +Since the 1980's live eggs of + +H. micropterus + +have been imported to Europe on at least three occasions, from +the Dominican +Republic, +Haiti +and +Tortola +Island +( +British Virgin Islands +). It was included on the Phasmid Study Group culture-list as culture No. 61 “ + +Aplopus + +sp.” (later corrected to + +Haplopus micropterus + +) and is fairly easy to rear in moderately humid but well ventilated conditions and high temperatures (> 25°C). In captivity it readily accepts rose ( + +Rosa + +spp., +Rosaceae +), bramble ( + +Rubus fruticosus + +, +Rosaceae +), raspberry ( + +Rubus idaeus + +, +Rosaceae +), oak ( + +Quercus robur + +& + +Q. petraea + +, +Fagaceae +), guava ( + +Psidium guajava + +, +Myrtaceae +), eucalyptus ( + +Eucalyptus gunnii + +, +Myrtaceae +) and hawthorn ( + +Pyracantha + +spp., +Rosaceae +) as alternative food plants. At least + +Malpighia gossipifolia +(Malpighiaceae) + +, + +Pictetia spinifolia +(Fabaceae) + +and + +Bidens cynapiifolia +(Asteraceae) + +are known to be part of the natural diet in Hispaniola. A REM-study of the egg was presented by Lipinski +et al. +(1999, fig. 25). + + +Lu +et al. +(in press) present comprehensive information on the distribution, food plants, habitats, biology and nymphal states of + +H. micropterus + +in the +Virgin Islands +and report + +Piscidia carthagensis +(Fabaceae) + +, + +Pictetia aculeata +(Fabaceae) + +and + +Pithecellobium unguis-cati +(Fabaceae) + +to serve as host plants. + + + +Distribution ( +Fig. 380 +): + +Virgin Islands +(St. Thomas [RMNH, MNHU, ZMUH]; St. Thomas (Loango [Werner, 1929: 7], Frenchman's Bay Esatate [Lu +et al. +in press], Estate Nazareth [Lu +et al. +in press]); St. Croix: Annaly [USNM]; St. Croix [NHMW]; +St. John +[MNHU]; +St. John +(Lameshur Ranger Station [Wenhua +et al. +In prep.]); +Tortola +, Long Bay, Belmont Estate [Lu +et al. +in press]; +Anegada +[USNM, Lu +et al. +in press]; Guana [NHMUK, USNM, Lu +et al. +in press]; Little Thatch [Lu +et al. +in press]; Moskito [Lu +et al. +in press]); +Puerto Rico +(Rincon [USNM]; Guánica [USNM]); Mona +Island +[USNM, ZMUH]; Hispaniola: +Dominican Republic +(Distrito Nacional [USNM]; Peravia Prov. [USNM]; Santo +Domingo +Prov. [IIBZ, MNHNSD, NHMUK, OXUM, USNM]; Pedernales Prov. [CMNH, FSCA, MNHN, MNHNSD, USNM]; Montecristi Prov. [USNM]; Barahona Prov. [FSCA, IIBZ, USNM]; Azua Prov. [MNHNSD, USNM]; Independencia Prov. [USNM]; Ocoa Prov. [USNM]; +San Cristóbal +Prov. [IIBZ, MNHNSD, USNM]; Macorís Prov. [MNHNSD]; La Vega Prov. [IIBZ]; +Isla +Beata [USNM]; +Isla +Saona [MNHNSD]); +Haiti +(Gros Morne [Moxey, 1972: 116, in litt.]; Furcy [ANSP]; Port-au-Prince [ANSP, NHMW, ZMUH]; Gonaive +Island +, Vicinity of Pointe-a-Raquettes [MCZC, Moxey, 1972: 116, in litt.]). + + +Number of specimens examined: +261 + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D359FFFCFF27ED94271F192D.xml b/data/38/7F/30/387F3068D359FFFCFF27ED94271F192D.xml new file mode 100644 index 00000000000..af88a0c0e73 --- /dev/null +++ b/data/38/7F/30/387F3068D359FFFCFF27ED94271F192D.xml @@ -0,0 +1,84 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + +Haplopus micropterus + +(St. Fargeau & + +Audinet-Serville, 1828) (Figs. 220–256, 340, 360, 380, 399–405) + + + +Cyphocrana microptera +St. Fargeau & Audinet-Serville, 1828: 445 + +. +HT +, ♀: St. Thomas [RMNH]. [Replacement name for + +Phasma angulata +Stoll, 1813 + +; +not + +Mantis angulata +Fabricius, 1793 + +] + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D365FFCCFF27EB27258E1961.xml b/data/38/7F/30/387F3068D365FFCCFF27EB27258E1961.xml new file mode 100644 index 00000000000..693c0d37c69 --- /dev/null +++ b/data/38/7F/30/387F3068D365FFCCFF27EB27258E1961.xml @@ -0,0 +1,627 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Diapherodes dominicae +(Rehn & Hebard, 1938) + +n. comb. + + + + +( +Figs. 109–119 +, +347 +, +366 +, +381 +) + + + + + +Diapherodes gigantea dominicae +Rehn & Hebard, 1938: 53 + +, pl. 4: 22 (♀). +HT +, ♀: +Dominica +, B. W. +I. +, +II.1927 +James Bond, + +Diapherodes gigantea dominicae + +, +Type +, R & H, ANSP 5539, WO188, = + +Diapherodes gigas +(Drury) + +, det. C.F. Moxey 1972 [ANSP, No. 5539]. + +Otte & Brock, 2003: 304. + + +Diapherodes gigas +, Moxey, 1971: 98 + +, 99 (in litt.; in part—only specimens from +Dominica +) + + + +Diapherodes gigantea +, Langlois & Lelong, 2010: 60 + +, figs. 19 (in part—only records from +Dominica +). + + + +Diapherodes + +sp. Lelong, Langlois, Rastel & Dorel, 2003: 48, figs. 19a–g (♀, ♂, nymph) & REM-photos 11–13 (egg). + + + + +Further material [6 ♀♀, 4 ♂♂, eggs]: + + +DOMINICA +: + + +1 ♀: +Dominica +1937, Walter H. Hodge; +USNM +; +ANSP +; w0187 [ +USNM +]; +1 ♂ +: +Dominica +, Clarke Hall, +7.II.1965 +; J.F.G. Clarke Thelma M Clarke; Bredin-Archold-Smithsonian Bio. Surv. +Dominica +; +USMNH +; w0189 [ +USNM +]; 1 ♀: Dominique, Croix, alt. +808 m +, +15°20’49’’N +61°18’23’’E +, +26X.2000 +[coll. +ASPER +, No. DOM00-101]; 2 ♂♂, 2 ♀♀, eggs: Dominique, Bellevue Mountain, alt. +455–533 m +, +15°37’22’’N +61°26’03’’E +, +29.X.2000 +[coll. +ASPER +, No’s DOM00-106 & 192 to 194]; 1 ♀: Dominique, Morne Macaque, alt. +762–855 m +, +15°20’31’’N +61°18’38’’E +, +20.X.2000 +[coll. +ASPER +, No. DOM00-190]; +1 ♂ +: Dominique, Picard River track, alt. +26–146 m +, +15°33’14’’N +61°27’06’’E +, +30.X.2000 +[coll. +ASPER +, No. DOM00-191]. + + + + +FIGURES 113–119. + +Diapherodes dominicae +(Rehn & Hebard, 1938) + +. +113. ♂ +head and pronotum: Guadeloupe, Picard River track [coll. ASPER]; +114. +♀ HT, head and pronotum [ANSP]; +115. +♂ apex of abdomen (lateral view) [coll. ASPER]; +116. +♂ apex of abdomen (dorsal view) [coll. ASPER]; +117. +Tegmina of ♂ [coll. ASPER]; +118. +Egg (lateral view), reproduced from REM-photograph by Lelong +et al. +(2003: appendix II, fig. 11); +119. +Egg (dorsal view), reproduced from REM-photograph by Lelong +et al. +(2003: appendix II, fig. 12). + + + + +Diagnosis: +Differing from all other members of the + +gigantea + +species-group of + +Diapherodes + +by the fairly obsolete cephalad spines, which are merely represented as rounded tubercles ( +Fig. 114 +). Females are similar to + +D. angulata +(Fabricius, 1793) + +from +Guadeloupe +but differ by: the smaller size; comparatively more slender legs; more numerous but smaller tubercles of the mesonotum; much smaller +anterior +pair of tubercles on the pronotum ( +Fig. 114 +); comparatively smaller spines of the longitudinal marginal row of the meso- and metapleurae and smaller not overlapping tegmina ( +Fig. 109–110 +). Males strongly resemble those of + +D. gigantea saintluciae + + +n. ssp. + +but differ by: the broader, laterally rounded and apically less acuminate vomer ( +Fig. 359 +); bright green legs (at best with a slight greenish hue in + +gigantea + +); greenish brown antennae and distinctive colouration of the +anterior +margin of the tegmina and alae, which is bright yellow and then gradually becomes dull green towards the interior ( +Fig. 117 +). From + +D. angulata + +♂♂ at once differ by the brown body, tegmina and alae as well as the strongly tuberculate mesonotum. + + + + + +Description: ♀ ( +Figs. 109–110 +). + +Fairly small members of the + +gigantea + +species-group (body length including subgenital plate 116.0 to +ca. +126.0 mm) and moderately robust for the genus (maximum body width at abdominal segment II 15.0– +16.8 mm +), with fairly small and slender tegmina (9.0–10.0 mm). General colouration plain apple green, the tubercles and granules of the head and thorax ochre to orange, the larger ones tipped with dull red or mars brown. Antennae straw and becoming mid brown towards the apex; two basal segments with a greenish hue. Ventral body surface dull green with a whitish hue. + + +Head: Vertex rounded, globose and armed with two ± decided, blunt tubercles, the posterior portion set with about ten small granules ( +Fig. 114 +). Eyes fairly small, circular in outline and their length contained almost +3x +in that of cheeks. Antennae with 51 antennomeres and roughly reaching to posterior margin of metanotum. + + +Thorax: Pronotum a little shorter but about as wide as head, the transverse median sulcus very pronunced and almost reaching to lateral margin of segment. A pair of low blunt spines +in anterior +portion and a pair of lower rounded tubercles at posterior margin; otherwise with a few granules in posterior half ( +Fig. 114 +). Mesothorax fairly short and roughly 1.5x longer than head and pronotum combined; posterior margin more than +2x +the width of +anterior +margin, the +anterior +portion gradually widened and the posterior half almost parallel-sided. Most parts of mesonotum irregularly set with fairly small spines and tubercles, which decrease in size towards the posterior; usually two pairs of somewhat enlarged but blunt spines close to +anterior +margin ( +Fig. 114 +) and 2–4 somewhat enlarged spines pre-medially. The lateral portions unarmed. Metanotum with a few very low granules +in anterior +portion. Spines of the marginal row of the meso- and metapleurae rather small and blunt, the largest spine not twice as long as its basal width; mesopleurae with 17–20 and metapleurae with about 10–12 spines ( +Figs. 109–110 +). Meso- and metasternum sparsely granulose. Tegmina fairly small and comparatively slender, hardly reaching posterior margin of metanotum, not overlapping and leaving a great space inbetween each other ( +Figs. 109–110 +). Alae much smaller and at best projecting underneath tegmina by +2 mm +. + + +Abdomen: Segment II about equal in length to median segment, widest part of body and very slightly widened towards the posterior; about 1.6x wider than long. III–VII gradually narrowing and roughly equal in length; VII with the lateral margins sometimes gently rounded. Sternites smooth and with two fine longitudinal carinae laterally. Praeopercular organ on sternum VII formed by a fairly decided tubercle and a C-shaped carina ( +Fig. 347 +). Tergum VIII narrowed medially and about 1.2x longer than wide. Anal segment narrowed towards the apex, hardly longer than wide and with posterior margin broadly rounded ( +Fig. 112 +). Epiproct very small and fully concealed by anal segment. Subgenital plate long and gradually narrowed towards a pointed tip; projecting over apex of abdomen by roughly the combined length of tergites IX and X ( +Figs. 111–112 +). + + +Legs: All of moderate length and fairly slender for the +gigantea +species-group. Meso- and metafemora with the outer carinae minutely granulose; medioventral carina with 6–8 fairly short but acute spines, two outer ventral carinae each with a single sub-apical spine. Posteroventral carina of meso- and metatibiae minutely denticulate. Anterodorsal carina with a low triangular lobe sub-basally and slightly triangularly expanded sub-apically. Basitarsi almost as long as following two tarsomeres combined. + + +♂. +Of moderate size (body length 82.0–98.0 mm) and fairly robust for the genus, with long alae (47.0–52.0 mm). Colouration of the body pale to mid brown, the ventral body surface dull ochre with a whitish wash; abdominal sternites slightly greenish and II–VII each with two black spots post-medially. Head dull ochre ( +Fig. 113 +), antennae greenish ochre. Legs mid green with the apex of all femora and tibiae dull green to mid brown. Thoracic armature dull green, the largest tubercles and spines tipped with very dark reddish brown. Tegmina and costal region of alae pale to mid brown with all veins dull green. +Anterior +margin of tegmina bright yellow, then gradually becoming green and the green section interiorly bordered by a dull bluish green longitudinal stripe ( +Fig. 117 +). Central hump dull brown. Basal portion of +anterior +margin of alae coloured like tegmina. Anal fan of alae transparent orange. + + +Head: About 1.2x longer than wide, the cheeks almost parallel-sided. Vertex gently rounded and with a pair of very low blunt tubercles, otherwise irregularly scattered with small, rounded granules ( +Fig. 113 +). Eyes circular in outline, projecting hemispherically and their length contained about 1.5x in that of cheeks. Antennae robust and consisting of 68 antennomeres. Scapus compressed dorsoventrally, 1.3x longer than wide with lateral margins decidedly deflexed and rounded. + + +Thorax: Pronotum about equal in length to head, the +anterior +margin decidedly wider than posterior margin and the transverse median sulcus very pronounced. +Anterior +portion with a pair of fairly distinct, blunt spines, the posterior portion with a pair of low tubercles behind transverse sulcus and a pair of slightly more distinct tubercles at posterior margin ( +Fig. 113 +). Mesothorax about 1.6x longer than head and pronotum combined. Mesonotum all over with irregularly scattered blunt tubercles, which decrease in size towards the posterior; two pairs of blunt spines near +anterior +margin ( +Fig. 113 +) and a longitudinal row of rounded tubercles along lateral margins. Meso- and metapleurae with a marginal row of differently sized blunt tubercles. Meso- and metasternum irregularly scattered with small granules and various low, rounded tubercles. Tegmina with central hump fairly pronounced and convex ( +Fig. 117 +). Alae reaching about half way along abdominal tergum VI. + + +Abdomen: Segments II–VII very slightly gradually narrowing and decreasing in length; tergum VII with the posterolateral angles gently deflexed. Tergum VIII strongly widened towards the posterior and trapezoidal in dorsal view; VIII–X with a longitudinal median carina, which is blunt on VIII and IX but fairly fine on X. Anal segment with lateral margins almost parallel-sided, the posterior margin with a broad and shallow median indentation ( +Fig. 116 +). Cerci with apical half round in cross section and the apex blunt. Vomer broad, rounded and with the apical portion gradually narrowing towards a fairly short apical hook ( +Fig. 366 +). Poculum with basal portion roundly convex ( +Fig. 115 +), otherwise fairly flat and with the posterior margin broadly rounded. + +Legs: All of moderate length and fairly robust; metafemora reaching about half way along abdominal segment IV and metatibiae reaching to posterior margin of abdominal segment VI. All outer carinae of mid and hind legs very minutely denticulate. Medioventral carina of mesofemora only with two fairly prominent and acute spines in apical portion in metafemora with five prominent spines, that decrease in size towards the base. Two outer ventral carinae each with a single sub-apical spine. Basitarsus about 1.3x longer than second tarsomere. + + +Egg ( +Figs. 118–119 +): + +Of moderate size (capsule length +4.78 mm +), capsule about 1.7x longer than wide. Polar area slightly impressed if seen in lateral aspect. Capsule surface to various degrees covered with irregular, distinctly raised areas covered with clusters of sponge-like structured tubercles and granules. These form a conspicuous longitudinal ridge from the posterior end of the micropylar plate to the polar-area. Opercular collar decidedly marginated. Micropylar plate rather large and about half as long as capsule. Entire surface, except for a stripe along the outer margin, covered with irregular granules and raised ridges. Centre with an elongate, impressed region. Micropylar cup distinct and placed in a very deep central gap of posterior margin of plate. Operculum in the centre with a prominently raised circular rim and a conical tubercle in the centre. General colouration pale brown. Outer margin of micropylar plate and micropylar cup darker brown. + +Measurements according to Lelong, Langlois, Rastel & Dorel (2003: 51) [mm]: Length 4.78, width 2.72, height 3.05, diameter of operculum 1.70. + + + +Comments: +Rehn & Hebard (1938: 53) described + +Diapherodes gigantea dominicae + +based on a single ♀ in ANSP, which was collected by the leading American ornithologist James Bond. They distinguished it from + +D. gigantea +(Gmélin, 1789) + +by the smaller size, smaller spines of the mesothorax (a very variable feature in + +gigantea + +), smaller spines of the meso- and metapleurae and unarmed carinae of the legs. But in fact, all these characters of the ♀♀ place it much closer to + +D. angulata +(Fabricius, 1793) + +from neighbouring +Guadeloupe +rather than + +D. gigantea + +from +Grenada +and +St. Vincent +. Males however differ from + +D. angulata + +by a good number of obvious features and rather resemble those of + +D. gigantea + +or + +D. martinicensis +Lelong & Langlois, 2005 + +. Consequently, detailed examination of Dominican specimens has shown these to represent a separate and valid species ( +n. comb. +). Moxey (1971: 99) erroneously synonymised + +D. gigantea dominicae +Rehn & Hebard + +with + +Diapherodes gigantea + +. + + +Lelong, Langlois, Rastel & Dorel (2003) provided detailed descriptions and illustrations of the adult ♀ and ♂, nymphs and eggs as well as information on the habitats and biology of + +Diapherodes dominicae + +in +Dominica +, their specimens being provisionally identified as “ + +Diapherodes + +sp.”. They stated this species to be not particularly abundant with only single specimens found in each prospected locality. In their natural habitats, which include montane and lowland hygrophilic forests as well as cultivated zones in xero-mesophilic environments, these insects are usually found at heights of 1.5–3 metres off the ground and feed on guava ( + +Psidium guajava + +, +Myrtaceae +) and mapou-baril ( + +Sterculia caribea + +, +Sterculiaceae +). In captivitiy in Europe Lelong, Langlois, Rastel & Dorel (2003: 48) reported it to accept bramble ( + +Rubus fruticosus + +, +Rosaceae +) as an alternative food-plant. + + + + + +Distribution ( +Fig. 381 +): + +Dominica +(Croix, +808 m +; Bellevue Mountain +455–533 m +& Picard River track, +26–146 m +) [USNM; coll. ASPER]. Endemic. + + + + +Number of specimens examined: +11 + + + +TABLE 12. +Measurements of + +Diapherodes dominicae +(Rehn & Hebard, 1938) + + +n. comb. + +[mm] + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+♀, HT + +dominicae + +[ANSP] +♀♀ *♂♂ *
Body (incl. sg. pl.)> 123.3116.0–120.0-
Body121.8-82.0–98.0
Pronotum7.05.5–6.03.5–4.0
Mesonotum24.720.5–21.013.0–17.0
Metanotum8.317.0–17.5**12.0–13.5**
Median segment9.1--
Tegmina9.79.0–10.010.0–12.5
Alae--47.0–52.0
Profemora22.020.0–21.012.0–18.0
Mesofemora18.517.011.0–12.5
Metafemora26.223.0–24.018.5–20.5
Protibiae20.1--
Mesotibiae16.0--
Metatibiae24.7--
Antennae> 33.546.0–47.045.0–56.0
+
+* according to Langlois & Lelong, 2010: 60 ** including the median segment +
+
+
\ No newline at end of file diff --git a/data/38/7F/30/387F3068D369FFCAFF27EA2926121A67.xml b/data/38/7F/30/387F3068D369FFCAFF27EA2926121A67.xml new file mode 100644 index 00000000000..31cf4fba6ba --- /dev/null +++ b/data/38/7F/30/387F3068D369FFCAFF27EA2926121A67.xml @@ -0,0 +1,1050 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Diapherodes gigantea gigantea +(Gmélin, 1789) + + + + + +( +Figs. 120–135 +, +348 +, +368 +, +381 +, +392–393 +, +396 +, +406–408 +) + + + + + +Mantis gigantea +Gmélin, 1789: 2055 + +. +HT +, ♀: +St. Vincent +; BMNH(E) #878212 [NHMUK]. [Replacement name for + +Mantis gigas +Drury, 1773 + +]. + + + +Diapherodes gigantea +, Kirby, 1904a: 362 + +. + +Rabaey, 2004: 10, figs. 1, 2 & plate figs. 1 (adult couple) & 2. + + +Diapherodes gigantea gigantea +Rehn & Hebard, 1938: 53 + +. + + +Otte & Brock, 2005: 120. [„ +Type +lost“] + + + +Mantis gigas +Drury, 1773: 89 + +, pl. 50 (♀). +HT +, ♀: +St. Vincent +; BMNH(E) #878212 [NHMUK]. [ +Junior homonym +of + +Gryllus +( +Mantis +) +gigas +Linné, 1758 + +] + + + +Diapherodes gigas +, Gray, 1835: 33 + +. + +Westwood, 1859: 84. + + + +Saussure, +1871–1872 +: 184. + +Brunner v. Wattenwyl & Redtenbacher, 1892: 208. +Brunner v. Wattenwyl, 1893: 606. +Redtenbacher, 1908: 434, pl. 20:1 (♀). + +Moxey, 1971: 98 (in litt.; in part—only specimens from +Saint Vincent +& +Grenada +). Bradley & Galil, 1977: 189. [ + +Mantis gigas +Drury, 1773 + +removed from homonymy] + + + + + +Phasma (Diapherodes) gigas +, Westwood, 1873: 100 + +, pl. 50 (♀). + + + +Cyphocrana cornuta +St. Fargeau & Audinet-Serville, 1825: 445 + +. +HT +, ♀: + +Diapherodes gigas +Drury + +, +Saint Vincent +[NHMUK]. [Unnecessary replacement name for + +Mantis gigas +Drury, 1773 + +→ +Junior objective synonym +of + +Mantis gigantea +Gmélin, 1789 + +] + + +[ +Not: + +Gryllus (Mantis) gigas +Linné, 1758: 425 + +; → Valid name: + +Phasma gigas +(Linné, 1758) + +, +Phasmatinae +: +Phasmatini +] + + +[ +Not: + +Haplopus grayi +Kaup, 1871: 36 + +, +erroneous synonym +of Moxey, 1971: 99] + + +[ +Not: + +Diapherodes gigantea dominicae +Rehn & Hebard, 1938: 53 + +, +erroneous synonym +of Moxey, 1971: 99] + + +[ +Not: + +Diapherodes gigas +, Langlois & Lelong, 1997: 43 + +, figs. 20a (♀) & 20 b (♂), misidentification à Specimens from +Guadeloupe +are + +Diapherodes angulata angulata +(Fabricius, 1793) + +]. + + +[ +Not: + +Diapherodes gigas +, Lelong & Langlois, 2001: 242 + +, figs. 1 (♀), 2 (♀), misidentification → Specimens from +Guadeloupe +are + +Diapherodes angulata angulata +(Fabricius, 1793) + +]. + + +[ +Not: +Langlois, Lelong & Dorel, 2006: 42, figs. 19 a–g (♂, ♀, nymph), photos 5–6 (♀) & 27–29 (egg, REM-photos) à here described as + +D. gigantea saintluciae + + +n. ssp. + +]. + + +[ +Not: +Langlois & Lelong, 2010: 69 à records from +Dominica +are + +D. dominicae +(Rehn & Hebard, 1938) + +]. + + +[ +Not: +Langlois & Lelong, 2010: 69 à records from +Saint Lucia +are + +D. gigantea saintluciae + + +n. ssp. + +]. + + + + +Further material [50 ♂♂, 52 ♀♀, 9 nymphs, eggs]: + + +SAINT VINCENT +: + + +1 ♀: +Saint Vincent +, W. I., H.H. Smith, Collectio Br. v. W., det. Br. V. W. + +Diapherodes gigas +Drury + +, 97. Said to be found principally in high trees: one specimen was obtained on a guava-tree. Second specimen wet in Nov. and one in May. In living specimens the ground colour is a pea-green, spines above brown, those at the legs black. [ +NHMW +, No. 838]; 1 ♀: +St.Vincent +, W. I., H.H. Smith, Collectio Br. v. W., det. Br. V. W. + +Diapherodes gigas +Drury + +, 18.737 [ +NHMW +, No. 838]; 1 ♀: +Saint Vincent +, W. I., H.H. Smith, 9b, +Saint Vincent +W. I., 95–206 ( +NHMUK +); +1 ♂ +: 321, +Saint Vincent +, W. I., H.H. Smith, Edge of Fonst. Sunfriese [Sufriére] Volcano, Leeward side +1200 ft +., +Jan. 5 +on leaf of + +Heliconia + +or “Wild Plantain”, + +Diapherodes gigas + +[ +NHMUK +]; +1 ♂ +: 40, 4-2, 1936, + +Diapherodes +G. R. Gray + +, + +Diapherodes gigas +(Drury) + +, +Saint Vincent +[wings spread] [ +NHMUK +]; 1 ♀: +Saint Vincent +, W. Indies, 1907-296, Pres. By Miss Patterson [ +NHMUK +]; 1 ♀: Sharp’s Valley, +Saint Vincent +, B.W.I., VIII.25.1941, R. S. Fennah [ +ANSP +]; 1 ♀: +Saint Vincent +, W. Indies, H.H. Smith; A.N.S.P., Ex Carn. Mus, Bruner Cln. [ +ANSP +]. + + +GRENADA +: + + +1 ♀: St. Georges, +Grenada +, +July 1969 +, Frank E. Miller; + +Diapherodes gigas +(Drury) + +, det. A Gurney 1969 [ +USNM +]; 1 ♀: +Grenada +, W. I., H.H. Smith, Collectio Br. v. W., det. Br. V. W. + +Diapherodes gigas +Drury + +, 19.660, +May 15. +Purchased. This species is often seen on the Cashew-tree (Anacardiaceaee) [ +NHMW +, No. 838]; +1 ♂ +(penultimate instar): Vendome Est. (Leeward side), +Grenada +, W. I., H.H. Smith, Vendome Estate Leeward, +1200 ft +. open place, +Sept. 8 +, on Guava bush [ +NHMUK +]; +1 ♂ +: +Grenada +W. I., H.H. Smith, +Grenada +W. I., 95-206, St. Catharinés Rictory (Winward), +500 ft +. +June 10 +, “Left hind wing used for drawing” Ragge [ +NHMUK +]; +1 ♂ +(nymph n3): West Indies: +Grenada +, Par. St. Andrew, Birch Grove, +8-VI-1990 +, coll. M.C. Thomas [ +FSCA +]; 1 ♀: +Grenada +, B.W.I. [ +ANSP +]; 1 ♀: +Grenada +, W. Indies, H.H. Smith; A.N.S.P., Ex Carn. Mus, Bruner Cln. [ +ANSP +]; +1 ♂ +: + +Diapherodes gigantea +(Gmélin, 1789) + +. Elevage +Grenade +Don Alexandre Lerch 2007, E. Delfosse +Dec.2007 +[ +MNHN +]; +1 ♂ +: M. Delfosse, +Grenade +, ♂ +3/12/2012 +[ +MNHN +]; +1 ♂ +: M. Delfosse, +Grenade +, ♂ +23/11/2012 +[ +MNHN +]; 1 ♀: M. Delfosse, +Grenade +, Elevage ♀ +22/07/2007 +[ +MNHN +]; 2 ♀♀: ex Zucht: K. Rabaey ( +Belgien +), urspr.: +Grenada +, +III.–VIII. 2004 +[coll. FH, No’s 0359-1 & 2]; 2 ♂♂: ex Zucht: F. Hennemann, urspr.: +Grenada +, +III.–VIII. 2004 +[coll. FH, No’s 0359-3 & 4]; 1 ♀, 2 ♂♂, 1 ♀ (subadult), 4 ♀♀, +1 ♂ +(nymphs), 1 Gynandromorph (subadult), eggs: ex Zucht: F. Hennemann, urspr.: +Grenada +, 2005 [coll. FH, No’s 0359-5 to 14 & E]; 7 ♂♂, 7 ♀♀: ex Zucht: F. Hennemann 2007/08, Herkunft: +Grenada +, leg. T. & P. James, PSG No. 260 [coll. FH, No’s 0359- 15 to 30]; 5 ♂♂, 2 ♀♀: ex Zucht: F. Hennemann 2009, Herkunft: +Grenada +, leg. T. & P. James, PSG No. 260 [coll. FH, No’s 0359-31 to 38]; 30 ♂♂, 26 ♀♀, eggs: ex Zucht. O. Conle, Herkunft: +Grenada +[coll. OC]. + + +TRINIDAD +[in error?]: + + +1 ♀: 89–69: +Trinidad +[ +NHMUK +]. + + +NO / UNPRECISE +DATA +: + + +1 ♀: no data [wings spread] [ +NHMUK +]; 1 ♀: 40, 4-2, 1329 [presumably from +Saint Vincent +] [ +NHMUK +]; 1 nymph (n1): 40, 4- 2, 1366 [presumably from +Saint Vincent +] [ +NHMUK +]; 1 nymph (n1): 40, 4-2, 1367 [presumably from +Saint Vincent +] [ +NHMUK +]; +2 eggs +: 40, 4-2, 1370 [presumably from +Saint Vincent +] [ +NHMUK +]; +4 eggs +: 40, 4-2, 1369 [presumably from +Saint Vincent +] [ +NHMUK +]; 1 ♀: 40, 4-2, 1365 [wings spread—presumably from +Saint Vincent +] [ +NHMUK +]; 1 ♀: 59-57, Vigors Coll. [ +NHMUK +]; 1 ♀: West Indies, H. A. Ballou [ +ANSP +]. + + + + +Diagnosis: +This is the largest and most southward distributed species in the genus. Females are well characterized by the ± expanded and dentate carinae of the mid and hind legs (metatibiae in particular, +Fig. 132 +) and sparse armature of the mesonotum ( +Fig. 126 +). From + +D. angulata +(Fabricius, 1793) + +from +Guadeloupe +it differs by: the larger size of both sexes; much less numerous spiniform tubercles of the mesonotum; decidedly longer but less numerous spines of the marginal row on the meso- and metapleurae ( +Figs. 126–127 +); much broader legs and prominently dentate, ± distinctly expanded carinae of the mid and hind legs of ♀♀ ( +Fig. 132 +). Males differ from those of + +D. angulata + +by: the brown general colouration ( +Figs. 123 +, +380 +); relatively shorter mesothorax; more prominent spiniform tubercles on the mesonotum and translucent orange anal region of the alae (hyalinous in + +angulata + +). Eggs principally differ by the considerably larger dimensions and less strongly sculptured capsule surface ( +Figs. 134–135 +). + + + + + +Description: ♀ ( +Figs. 120–122 +, +392–393 +). + +Large to very large (body length including subgenital plate 153.0–197.0 mm) and broad for the genus (maximum body width at abdominal tergum II 15.0–19.0 mm), mid and hind legs with carinae ± expanded and denticulate (metatibiae in particular). General colouration usually plain bright apple-green, the ventral body surface mid green and with a whitish wash on abdominal sternites II–VII, more rarely with a black wash; occasionally olive or slightly brownish green specimens occur. Transverse borders between the abdominal tergites yellow to orange. Spines of the marginal expansion of the meso- and metapleurae dull pink to purple (bluish green in young specimens). Dorsal spines of the thorax with the bases yellow and tips orange. Antennae orange to reddish brown; scapus green. Tegmina and alae bright green. Tarsi yellowish or greenish pale to mid brown. Eyes yellowish to reddish brown. + + +Head: Globose, convex, 1.2x longer than wide and armed with two more or less decided humps, tubercles or blunt spines on vertex ( +Fig. 124 +). Back with a variable number of small granules, which are roughly arranged in four parallel, longitudinal rows; +anterior +portion sometimes set with a few scattered granules. Eyes circular, convex and rather small; their length contained almost 2.5x in that of cheeks. Antennae reaching to abdominal segment III; with about 55 segments. Scapus dorsoventrally flattened, 2.2x longer than wide and gently narrowed towards the base. Pedicellus cylindrical and about 2/5 the length of scapus. + + +Thorax: Pronotum slightly shorter and narrower than the head; indistinctly longer than wide. In front of the very prominent transverse median sulcus armed with a pair of large, blunt spines ( +Fig. 124 +); posterior half with a more or less decided pair of tubercles close to posterior margin (sometimes lacking). Mesothorax almost +2x +longer than head and pronotum combined, and moderately constricted anteriorly. Mesonotum dorsally armed with one or two pairs of prominent blunt spines close to +anterior +margin and one or two further pairs of slightly smaller spines in the +anterior +half of the dorsal surface; sometimes specimens may occur which lack any distinct spines and have the mesonotum with only a few small granules ( +Figs. 124, 126 +). Metanotum unarmed, about 2/5 length of mesonotum, gently narrowing towards the posterior and about as long as wide. Spines of the meso- and metapleurae very distinct and acute; the longest being almost 3.5x as long as its basal width ( +Figs. 126-127 +). Mesopleurae with 11–17, metapleurae with 11–14 spines. Meso- and metasternum each with a variable number of pointed tubercles ( +Fig. 127 +), which are generally more decided and larger on the metasternum. Tegmina fairly large for the genus and usually reaching to posterior margin of metanotum (length +11.6–15.3 mm +) with posterior margin roundly angulate; usually leaving a space inbetween them and rarely overlapping. Alae very small and projecting underneath tegmina by about 1.0–3.0 mm. + + +Abdomen: Median segment slightly longer than metanotum and trapezoidal, being gently narrowed towards the margin. Segments II–V of equal length, VI–VII slightly shorter. Lateral margins of III–V gently rounded. II–IV about 1.5–1.8x wider than long, V about as long as wide, VI slightly longer than wide. VII narrower and slightly longer than VI with the lateral margins ± rounded posteriorly. Praeopercular organ on sternum VII formed by a short, elongated carina which terminates in a blunt tubercle ( +Fig. 348 +). Tergum VIII about 3/5 the length and decidedly narrower than VII, considerably more convex than previous. IX less than half the length of VIII, roughly quadrate. Anal segment longer than IX, the posterior half gently narrowing towards the apex and with a faint longitudinal median carina dorsally. Posterior margin rounded and with a small, triangular median indentation ( +Fig. 131 +). Subgenital plate long and gradually narrowed towards a pointed tip; projecting over apex of abdomen by about the combined length of tergites IX and X ( +Figs. 130–131 +). + + +Legs: All of moderate length and strikingly broad, with several of the carinae of the mid and hind legs ± elevated. Profemora about as long as mesothorax and metatibiae reaching about half way along abdominal tergum VII. Posterodorsal carina of profemora with a few minute granules; remaining carinae of front legs unarmed. Mid and hind legs strongly carinate with all carinae densely and ± distinctly denticulate to roughly dentate ( +Fig. 132 +). Femora with posterodorsal and anteroventral carina ± strongly expanded and lamellate or ledge-like. Medioventral carina faint and with 5–11 spines, which decrease in size towards the base of femur. Posteroventral carina with one, anteroventral carina with two moderately distinct, pointed sub-apical spines. Anterodorsal carina of tibiae raised and ± elevated and rounded apically. Medioventral carina prominently raised and strongly rounded sub-basally. Armature and expansions considerably more decided on hind legs. Basitarsi indistinctly longer than second tarsomere. + + + +♂ ( +Figs. 123 +, +396 +). + +Large (body length 92.0–126.0 mm) and moderately stocky for the genus, with long alae (50.0– +69.5 mm +) and a comparatively short sparsely spinose mesothorax. General colouration of head and body pale yellowish to creamish mid brown; ventral body segments whitish. Thoracic armature mid to dull green ( +Fig. 125 +). Tegmina and costal region of alae creamish mid brown, the tegmina with a broad, longitudinal white stripe along the +anterior +margin, continued in the basal quarter of the alae. Anal region of alae pale translucent orange. Antennae reddish brown, two basal segments brown. Eyes dark reddish brown. + + + +FIGURES 120–123. + +Diapherodes gigantea gigantea +(Gmélin, 1789) + +. +120. +♀: Saint Vincent [NHMW, No. 838]; +121. +♀: captive reared from Grenada [coll. FH, No. 0359-1]; +122. +♀: captive reared from Grenada [coll. FH, No. 0359-28]; +123. +♂, captive reared from Grenada [coll. FH, No. 0359-33]. + + + +Head: Generally as in ♀♀, vertex strongly convex with two ± distinct cephalad tubercles or small spines and a few scattered small granules in posterior portion ( +Fig. 125 +). Eyes large, very slightly oval in outline and projecting hemispherically; their length contained slightly less than +2x +in that of cheeks. Antennae reaching to posterior margin of abdominal tergum III, otherwise as in ♀♀ and with 54–56 antennomeres. + + + +FIGURES 124–135. + +Diapherodes gigantea gigantea +(Gmélin, 1789) + +. +124. +♀ head and pronotum [coll. FH, No. 0359-29]; +125. +♂ head and pronotum [coll. FH, No. 0359-33]; +126. +♀ mesothorax (dorsal view) [coll. FH, No. 0359-29]; +127. +♀ mesosternum [coll. FH, No. 0359-29]; +128. +♂ apex of abdomen (lateral view); +129. +♂ apex of abdomen (dorsal view); +130. +♀ apex of abdomen (lateral view); +131. +♀ apex of abdomen (dorsal view); +132. +Right hind leg of ♀ from Grenada (posterolateral view) [coll. FH, No. 0359-1]; +133. +Right hind leg of ♂ from Grenada (posterolateral view) [coll. FH, No. 0359-33]; +134. +Egg (dorsal view) [coll. FH, No. 0359-E] +135. +Egg (lateral view) [coll. FH, No. 0359-E]. + + + +Thorax: Pronotum about as long and broad as head and gently narrowed towards the posterior. Transverse median sulcus very prominent, slightly curved and reaching lateral margins of segment. +Anterior +half armed with a median pair of spiniform tubercles or blunt spines; posterior margin with four small, but acute granules, two median ones and one at each outer angle ( +Fig. 125 +). Mesothorax of moderate length, about 1.7–1.8x longer than head and pronotum combined; mesonotum about +5x +longer than wide. Dorsal surface irregularly set with a variable number of small tubercles and granules; a longitudinal row of small granules along lateral margins. +Anterior +of mesonotum with two pairs of rather distinct blunt spines ( +Fig. 125 +), and usually there is a further pair of ± enlarged pre-median spiniform tubercles. Meso- and metapleurae with a longitudinal row of minute granules. Meso- and metasternum sparingly granulose. Tegmina with a blunt but well decided hump pre-medially. Alae reaching about half way along abdominal tergum VI. + + +Abdomen: Segments II–VII very slightly tapering gradually, II–IV roughly equal in length and V–VII somewhat decreasing in length. Tergum VII very slightly widened towards the posterior and occasionally with the lateral margins slightly deflexed and rounded posteriorly ( +Fig. 128 +). Tergum +VIII 2 +/3 the length of VII and gradually widening towards the posterior. IX ¾ the length of VIII and gently narrowing towards the posterior. Anal segment with a very faint longitudinal median keel, the posterior margin broadly rounded and with a ± distinct median indentation ( +Fig. 129 +). Vomer about 1.3x longer than maximum width, basal portion broadly rounded, the terminal hook straight acutely pointed of moderate length and bluntly keeled ventrally ( +Fig. 368 +). Poculum granulose, convex and cup-like with a blunt central hump and a small median incision at posterior margin ( +Fig. 368 +) and very slightly projecting over posterior margin of tergum IX ( +Fig. 128 +). + + +Legs: All of moderate length, profemora almost as long as pro- and mesonotum combined, metatibiae almost reaching to posterior margin of abdominal tergum VI. All carinae densely but very minutely denticulate. Posteroventral carina of meso- and metafemora with one, anteroventral carina with two sub-apical spines. Medioventral carina broad and flat, armed with 4–8 short but strong spines in apical half of femur, which strongly decrease in size and disappear about halfway towards the base ( +Fig. 133 +). Tarsi rather stout, slightly less than half the length of corresponding tibia. Basitarsi about 1.3x longer than second tarsomere. + + +Nymphs: +Newly hatched nymphs are rather robust and have a body length of ±20.0 mm. The colouration is mid green, the body dorsally marbled with some brown and the pronotum with a brown longitudinal median stripe. Coxae, protibiae and antennae brown. Later instars vary from pale green over straw to dark brown and sometimes specimens may possess bold whitish markings on the thorax and abdomen. The sexes can be distinguishes from 3rd instar onwards, but both have abdominal tergum VII with a rounded lateral lobe throughout their entire development which only disappears with the final ecdysis. + + +Variability: +This species shows considerable variability in the size and degree of the body and leg armature. Specimens from the type-locality +Saint Vincent +are on average larger and have the body and leg armature more prominently developed, particularly in ♀♀. While the mesonotum is unarmed or only bears a few moderately distinct spines in ♀♀ from +Grenada +, it is armed with 6–8 prominent, blunt spines in specimens from +Saint Vincent +. The distinct pair of tubercles on the vertex seen in ♀♀ from +Saint Vincent +is often lacking in the +Grenada +colony. The degree of expansion of the carinae of the mid and hind legs and the degree of leg armature of ♀♀ generally depends on the general size of the insects. The colouration of ♀♀ is usually bright apple-green, but more rarely olive or slightly brownish green specimens may occur. + + + +Egg ( +Figs. 134–135 +): + +The following description is based on a large number of eggs in the first author's collection (coll. FH) laid by captive reared specimens originating from +Grenada +. + + +Large, barrel-shaped and fairly elongate, capsule almost +2x +longer than wide. Polar area very gently impressed if seen in lateral aspect. Capsule surface to a variable degree covered with irregular areas and clusters of slightly sponge-like structured tubercles and raised ridges, as well as numerous single wart-like tubercles. These often form a ± decided longitudinal ridge from the posterior end of the micropylar plate to the polar-area. Opercular collar decidedly marginated. Micropylar plate rather large and slightly less than half the length of capsule. Entire surface, except for a narrow space along the outer margin, covered with the same sponge-like structures seen on the capsule. Micropylar cup distinct. Operculum in the centre with a prominent, raised circular rim, dorsally with ± spiniform tubercles. General colouration pale to dark brown, the raised structures often paler brown than lower parts of capsule. Outer margin of micropylar plate and micropylar cup blackish brown. + +Measurements [mm]: Length including operculum 4.9–5.8, length 4.7–5.6, width 2.9–3.3, height 2.9–3.2, length of micropylar plate 1.8–2.2. + + + +Comments: +This striking species was first described by Drury (1773: 89) as + +Mantis gigas + +. As Drury's species was at that time placed in the same genus as + +Gryllus (Mantis) gigas +Linné, 1758 + +, Gmélin (1789: 2055) was in his rights to introduce + +Mantis gigantea + +as a replacement name for Drury's species. Although these two taxa were placed in two distinct genera subsequently, Gmélin's + +Mantis gigantea + +is the valid name of the species originally described and figured by Drury. With the exceptions of Kirby (1904a), Rehn & Hebard (1938) and Otte & Brock (2003) Gmélin's valid replacement name was not accepted by subsequent authors who all listed + +Mantis gigantea +Gmélin, 1789 + +as a junior synonym of + +Mantis gigas +Drury, 1773 + +. Drury's ♀ type-specimen was believed lost, but a ♀ in NHMUK with the data “ + +Diapherodes gigas +Drury + +, +Saint Vincent +” matches perfectly with the illustration provided by Drury (1773, plate 50) in every aspect, hence is here interpreted as the +holotype +of + +Mantis gigas +Drury. + + + + +Haplopus grayi +Kaup, 1871 + +(most certainly from +Guadeloupe +, → see comments on + +D. angulata + +above) and + +Diapherodes gigantea dominicae +Rehn & Hebard, 1938 + +from +Dominica +were both erroneously interpreted as synonyms of + +Diapherodes gigas +(Drury, 1773) + +in the unpublished PhD-Thesis of Moxey (1971: 99). In fact, + +H. grayi + +is a synonym of + +D. angulata +(Fabricius, 1793) + +and + +D. gigantea dominicae + +is here shown to represent a separate and valid species (→ see + +Diapherodes dominicae +Rehn & Hebard, 1938 + + +n. comb. + +). Redtenbacher (1908: 434, pl. 20: 1) provided brief descriptions of both sexes and illustrated a ♀ from +Saint Vincent +in NHMW. + + +Examination of numerous specimens throughout European and American museum collections has proven + +D. gigantea + +is restricted to the two southern Lesser Antillean islands +Grenada +and +Saint Vincent +. No specimens have so far been recorded from the intervening +Grenadines +and a specimen from +Trinidad +in NHMUK is most certainly mislabelled. All records from +Guadeloupe +and +Dominica +were based on misidentified material of either + +D. angulata +(Fabricius, 1793) + +or + +D. dominicae +(Rehn & Hebard, 1938) + +. The specimens recorded from +Saint Lucia +by Langlois, Lelong & Dorel (2006: 42) and Langlois & Lelong (2010: 69) are here described as a separate subspecies ( + +D. gigantea saintluciae + + +n. ssp. + +), since these differ by a good number of morphological characters from specimens from +Grenada +and +Saint Vincent +(→ see below). + + +In +Grenada +this species is known to feed on cinnamon ( + +Cinnamomum + +spp., +Lauraceae +) and guava ( + +Psidium guayava + +, +Myrtaceae +). Hand-written labels underneath the specimens from +Saint Vincent +and +Grenada +in NHMW state these insects to be principally found on high trees and to be commonly observed on cashew-trees ( + +Anacardium occidentale +, Anacardiaceaee + +). Hence, this might be another natural host-plant of + +D. gigantea gigantea + +. Based on a record of a museum specimen, Moxey (1972: 10) furthermore mentioned + +Ixora + +sp. ( +Rubiaceae +) to be a possible host-plant. + + +Rabaey (2004) provided brief information on the distribution in +Grenada +, alternative food plants and breeding of + +D. gigantea + +. In captivity in Europe nymphs and adults accept eucalyptus ( + +Eucalyptus + +spp., +Myrtaceae +), bay tree ( + +Laurus nobilis + +, +Lauraceae +), guava ( + +Psidium guajava + +, +Myrtaceae +), salal ( + +Gaultheria shallon + +, +Ericaceae +), different oaks ( + +Quercus + +spp., +Fagaceae +) and bramble ( + +Rubus fruticosus + +, +Rosaceae +) as alternative food plants. Adults are fairly robust and long-lived insects, ♀♀ reaching ages of up to one year. Mating is frequent but mainly takes place during the night. On average ♀♀ lay two eggs per day, which are simply flicked away by a rapid movement of the abdomen. The strong and ventrally spinose hind-legs of ♀♀ are frequently used for active defense, whereas ♂♂ flash their large orange wings. This species has been included on the Phasmid Study Group (PSG) culture-list as culture No. 260. + + +Photos of an interesting captive reared gynandromorph have been contributed by Mieke Duytschaever ( +Belgium +). This specimen is a mainly ♂ but has several ♀ characteristics on the right. While there is a fully developed ala on the left, the right ala is only represented as a small scale-like rudiment. All right legs and most parts of the right body surface a bright geen as in ♀♀, the remaining portions of the body being brown as typical for ♂♂ of this species ( +Figs. 406–407 +). The genitalia are mostly ♂ with a typical anal segment, but the poculum is considerably deformed ( +Fig. 408 +). + + + + + +Distribution ( +Fig. 381 +): + +Saint Vincent +[Volcano Soufriére [NHMUK]; Sharp's Valley [NHMUK]) and +Grenada +(St. Georges [USNM]; Vendome Estate [NHMUK]; St. Andrew, Birch Grove [FSCA]). + + + + +Number of specimens examined: +111 + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D36EFFD6FF27EA1621E51AAE.xml b/data/38/7F/30/387F3068D36EFFD6FF27EA1621E51AAE.xml new file mode 100644 index 00000000000..c23a98a6779 --- /dev/null +++ b/data/38/7F/30/387F3068D36EFFD6FF27EA1621E51AAE.xml @@ -0,0 +1,500 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Diapherodes gigantea saintluciae + +n. ssp. + + + + +( +Figs. 136–143 +, +367 +, +381 +) + + + + + +Diapherodes gigantea +, Langlois, Lelong & Dorel, 2006: 42 + +, figs. 19 a–g (♂, ♀, nymph), photos 5–6 (♀) & 27–29 (egg, REMphotos). + + +Langlois & Lelong, 2010: 60 (in part—only records from +Saint Lucia +). + + + + +HT +, ♀: +Saint Lucia +, Mount Rochar +1100 ft +., Nr. Dennery, 22.30 local time, 1994, on guava on side of track, AR + DP James [NHMUK]. + + +PT +, 2 ♀♀: +Santa Lucia +89–99 [NHMUK]. + + +PT +, ♂: +Saint Lucia +, Prospect, +9.VI.1936 +, H.E. Box, Pres. by Com. Inst. Ent. B. M. 1952-302 [NHMUK]. + + +PT +, ♂: +Saint Lucia +, Castries, +9.XI.1934 +, H.E. Box, Pres. by Com. Inst. Ent. B. M. 1952-302 [NHMUK]. + + +PT +, ♂: La Perle Estate, +Saint Lucia +, W. Indies, J. Frew, B. M. 1935-270, + +Diapherodes + +sp. not in B. M. det. B. Uvarov 1935 [NHMUK]. + + +PT +, ♂: +Saint Lucia +: Union Agr. School, +25-V-1987 +, R.E. Woodruff [FSCA]. + + +PT +, +1 ♂ +, 1 ♀: +Sainte-Lucie +, Barre de l’Isle Trail, alt. +275–305 m +, +13°55’34’’N +60°57’28’’E +, +02.XI.2003 +[MNHN, coll. ASPER; No’s SLU03-90 & 94]. + + +PT +, 3 ♀♀: +Sainte-Lucie +, Barre de l’Isle Trail, alt. +275–305 m +, +13°55’34’’N +60°57’28’’E +, +02.XI.2003 +[coll. ASPER; No’s SLU03-91 to 93]. + + +PT +, ♀: +Sainte-Lucie +, Mount Beaujolais nord, alt. +38–274 m +, +13°54’30’’N +60°55’45’’E +, +22.X.2003 +[coll. ASPER, No. SLU03- 18]. + + +PT +, 2 ♂♂: +Sainte-Lucie +, Banse +1 km +nord, alt. +183–229 m +, +13°47’09’’N +60°58’53’’E +, +21.X.2003 +[coll. ASPER, No’s SLU03- 98 to 99]. + + +PT +, ♂: +Sainte-Lucie +, Forestière, alt. +185–305 m +, +13°57’29’’N +60°57’46’’E +, +29.X.2003 +[coll. ASPER, No. SLU03-074]. + + + + +Diagnosis: +Similar to the nominate form from +Saint Vincent +and +Grenada +but, apart from being geographically isolated, easily distinguished by the considerably smaller size, relatively shorter mesothorax and more numerous spiniform tubercles and spines of the mesonotum of both sexes. Females differ by: the more broadened mesothorax; longitudinal row of small spines near the lateral margins of the mesonotum ( +Figs. 136–137 +); more numerous granules and tubercles of the meso- and metasternum; lack of the distinct lamellate expansions of the mid and hind legs, as well as the almost smooth dorsal carinae of the meso- and metafemora and corresponding tibiae. ♂♂ differ from those of the nominate form by: the black mesothoracic armature; somewhat longer alae, which usually exceed the posterior margin of abdominal tergum VI ( +Figs. 138–139 +); broader posteromedian excavation of the anal segment ( +Fig. 143 +) and broader vomer, which has the terminal hook somewhat less acuminate and relatively shorter ( +Fig. 359 +). One of the ♂ +paratypes +(specimen from Prospect in NHMUK) has a rounded posterolateral lobe on abdominal tergum VII and the meso- and metafemora bear a sub-apical lobe dorsally, both of which features are also not known to occur in + +D. gigantea gigantea + +. The characterizations provided below emphasize on the distinctive features. + + + + +Etymology: +Neuter. The name “ +saintluciae +” refers to the type-locality +Saint Lucia +, one of the Lesser Antillean islands, to which this new subspecies is endemic. + + + +Characterization: ♀ ( +Figs. 136–137 +). + +Of moderate size for the genus (body length including subgenital plate 118.5–132.0 mm), and fairly broad (body width at abdominal tergum III 11.0–14.0 mm). General colouration bright yellowish green to apple green, ventral body segments mid green with a slight whitish wash on abdominal sternites. All larger spines and spiniform tubercles of the thorax dull yellow with black tips. Meso- and metapleurae white ventrally with the longitudinal row of spines dark red to dull reddish brown. Antennae pale red, the scapus and pedicellus with a brownish hue. Eyes of moderate size, slightly elongate-oval; their length contained about 2.5x in that of cheek. Pronotum with a prominent median pair of blunt spines in the +anterior +half; posterior half armed with one or two pairs of blunt tubercles medially and a small, spiniform tubercle at each posterolateral angle. Mesothorax rather short and decidedly, gradually widened towards the posterior; about 1.4x longer than head and pronotum combined; mesonotum with posterior margin more than +2x +wider than +anterior +margin ( +Figs. 136–137 +). Dorsal surface of mesonotum armed with two distinct pairs of spines close to +anterior +margin and a variable number of spines and spiniform tubercles in the remainder portion except the posterior 1/3; usually with two considerably enlarged spines medially. Along lateral margins with a longitudinal row of 6–12 moderately sized spines, which gradually decrease in size towards the posterior of segment ( +Figs. 136–137 +). Spines of the meso- and metapleurae acute and of moderate size, the largest spine less than +2x +as long as its basal width. Meso- and metasternum unevenly tuberculose. Abdominal tergum VII ± deflexed with lateral margins gently rounded ( +Fig. 141 +). Posterior margin of anal segment broadly rounded, epiproct very small and fully hidden under anal segment ( +Fig. 141 +). Subgenital plate long and projecting over apex of abdomen by more than the combined length of tergites IX and X +Figs. 140–141 +). Posterodorsal carina of profemora, as well as all carinae of the mid and hind legs finely but acutely granulose. Medioventral carina of meso- and metafemora faint and with 6–10 stout but distinct spines, which decrease in size towards the base of femur. Posteroventral carina with one, anteroventral carina with two moderately distinct, pointed sub-apical spines. + + + + + +♂ ( +Fig. 138–139 +). + +Medium-sized for the genus (body length 83.0–89.0 mm). General colouration creamish mid brown, the ventral body segments except the prosternum whitish. Spines of the pro- and mesonotum black with olive bases, all smaller tubercles and granules of the thorax black. Antennae ochre. +Anterior +margin of tegmina and +anterior +margin in basal portion of alae pale yellow. If present, sub-apical dorsal lobes of the meso- and metafemora very dark brown. Vertex armed with two moderately decided ochre tubercles, back of vertex smooth. Pronotum with a well developed pair of blunt spines in front of the transverse median depression, and a pair of considerably smaller, spine-like tubercles in the posterior portion. Mesothorax about +2x +longer than head and pronotum combined. Mesonotum dorsally armed with 8–12 distinct but blunt paired spines and usually a cluster of four paired spines close to +anterior +margin; posterior portion of dorsal surface irregularly covered with small, acute granules; a variable number of blunt tubercles present along lateral margins. Mesopleurae with a longitudinal row of 8–10 rather distinct tubercles, which gradually decrease in size towards the posterior. Alae reaching to or projecting over posterior margin of abdominal tergum VI. Anal region of alae pale transparent pink. Abdominal tergum VII either parallel-sided or with a rather distinct, rounded lobe posterolaterally. Anal segment with a broad but shallow posteromedian excavation ( +Fig. 143 +). Vomer roundly triangular, hardly longer than wide and with a fairly short and broad, acuminate apical hook ( +Fig. 367 +). Poculum with a distinct median incision at posterior margin ( +Fig. 367 +). Posterodorsal carina of meso- and metafemora sometimes with a ± prominent, roundly triangular lobe sub-apically; anterodorsal carina of meso- and metatibiae occasionally expanded and rounded subbasally and sub-apically. Spines on the medioventral carina of the meso- and metafemora fairly small. + + + +FIGURES 136–139. + +Diapherodes gigantea saintluciae + +n.ssp +.. +136. +♀ PT: Saint Lucia, Barre de l’Isle Trail [coll. ASPER]; +137. +♀ PT: Saint Lucia, Barre de l’Isle Trail [coll. ASPER]; +138. +♂ PT: Saint Lucia, Barre de l’Isle Trail [coll. ASPER]; +139. +♂ PT: Saint Lucia, Union Agricultural School [FSCA]. + + + +Variability: +Both sexes show some variability in the size and number of the mesothoracic spines. The ♂ from Prospect in NHMUK is characteristic for having the lateral margins of abdominal tergum VII with a rounded posterior lobe, having a roundly triangular sub-apical lobe on the posterodorsal carina of the meso- and metafemora and having the anterodorsal carina of the meso- and metatibiae roundly to triangularly expanded sub-basally and sub-apically. + + + + +FIGURES 140–143. + +Diapherodes gigantea saintluciae + +n.ssp +.. +140. +♀ apex of abdomen (lateral view) [coll. ASPER]; +141. +♀ apex of abdomen (dorsal view) [coll. ASPER]; +142. +♂ apex of abdomen (lateral view) [coll. ASPER]; +143. +♂ apex of abdomen (dorsal view) [coll. ASPER]. + + + + +Comments: +Langlois, Lelong & Dorel (2006: 42) and Langlois & Lelong (2010: 69) reported + +D. giagntea saintluciae + + +n. ssp. + +is not particularly common on +Saint Lucia +with merely nine specimens found at four of the thirteen prospected localities. However, these authors stated it was comparatively more abundant than other + +Diapherodes + +-species are on neighbouring islands. + +Diapherodes gigantea saintluciae + + +n. ssp. + +occurs in various biotopes like montane and lowland hygrophilic forests as well as cultivated zones in xero-mesophilic environments and is usually found in vegetation 0.5–4 metres off the ground. In the wild +mimosa +( + +Mimosa camporum + +, +Mimosaceae +), guava ( + +Psidium guajava + +, +Myrtaceae +) and mapou-baril ( + +Sterculia caribea + +, +Sterculiaceae +) seem to represent natural food plants. Captive rearing in Europe has shown bay tree ( + +Laurus nobilis + +, +Lauraceae +) and bramble ( + +Rubus fruticosus + +, +Rosaceae +) to be accepted as alternative food plants by both nymphs and adults. + + + + + +Distribution ( +Fig. 381 +): + +Saint Lucia +(Mount Rochar, nr. Dennery +1100 ft +. [NHMUK]; Prospect [NHMUK]; Castries [NHMUK]; La Perle Estate [NHMUK]; Trail above Banse +183–229 m +[ASPER]; Northern Mount Beaujolais +38–274 m +[ASPER]; Forestière [ASPER]; Barre de l’Isle Trail +274–305 m +[MNHN, ASPER] & Union Agricultural School [FSCA]). Endemic. + + + + +Number of specimens examined: +16 + + + +TABLE 14. +Measurements of + +Diapherodes gigantea saintluciae + + +n. ssp. + +[mm] + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
♀, HT [NHMUK]♂, PT [FSCA]♀♀, PT* ♂♂, PT* [MNHN & coll. [MNHN & coll. ASPER] ASPER]
Body (incl. sg. pl.)124.5-123.0–132.5 -
Body119.082.0- 86.0–89.0
Pronotum5.53.05.5–6.0 3.0–3.5
Mesonotum19.612.021.0–25.0 12.5–14.0
Metanotum8.2-8.0–10.0** 13.0–14.0**
Median segment10.0-
Tegmina9.811.210.5–13.0 10.5–12.0
Alae5.046.5- 48.0–50.0
Profemora19.614.521.0–23.0 14.5–15.0
Mesofemora18.312.920.0–22.5 13.5–14.0
+
+ +......continued on the next page + +
+
+
\ No newline at end of file diff --git a/data/38/7F/30/387F3068D372FFDCFF27ECF325A91F71.xml b/data/38/7F/30/387F3068D372FFDCFF27ECF325A91F71.xml new file mode 100644 index 00000000000..74688a0c2df --- /dev/null +++ b/data/38/7F/30/387F3068D372FFDCFF27ECF325A91F71.xml @@ -0,0 +1,563 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Diapherodes martinicensis +Lelong & Langlois, 2005 + + + + + +( +Figs. 144–156 +, +349 +, +369 +, +381 +, +394–395 +) + + + + + +Diapherodes + +sp. Langlois, Lelong, Polidori & Dorel, 2000: 46, figs. 19a–g (♀, ♂, nymph) & photos 10–12 (egg). + + + + + +Diapherodes martinicensis +Lelong & Langlois, 2005: 264 + +, figs. 19–23 (♀, ♂, nymph), 40–42 (egg). +HT +, ♀: +Martinique +, trace Duclos, +10/XI/98 +, ref. No. +MAR98 +-036 [MNHN]; +AT +, ♂: +Martinique +, Morne-Rouge, +15.X.1960 +, + +Diapherodes dominicae + +—Rehn et Hebard [coll. Pére Pinchon, Hôtel de Région +Martinique +]; +PT +, ♀: +Martinique +, Balata, +18.III.1963 +[coll. Pére Pinchon, Hôtel de Région +Martinique +]; +PT +, ♀: +Martinique +[coll. H. Griffon, +Martinique +]. + + + + +Further material [16 ♂♂, 18 ♀♀, 2 nymphs, eggs]: + + +MARTINIQUE +: + + +7 ♂♂, 6 ♀♀, 1 ♀ (n5), 1 ♀ (n4), eggs: ex Zucht F. Hennemann +2014–2015 +, Herkunft: +Martinique +, leg. C.B. Dupré 2011 [coll. FH, No’s 0750-1 to 15 & E]; 9 ♂♂, 12 ♀♀, eggs: ex Zucht. O. Conle, Herkunft: +Martinique +[coll. OC]. + + + + +Diagnosis: +This is the smallest species of the + +gigantea + +species-group and apart from the small size (body length of ♀♀ < +10 cm +) well distinguished from all other representatives by: the short mesothorax, which is strongly gradually broadened towards the posterior, trapezoidal in dorsal aspect and swollen dorsally with a prominent central pair of spines in ♀♀ ( +Fig. 144 +); completely unarmed tibiae of both sexes; having only 37 antennomeres in ♀♀ (at least +50 in +all other species); relatively shorter legs with the hind legs of ♀♀ not projecting over abdominal tergum VI, as well as the long alae of ♂♂ which at least reach to the posterior margin of abdominal tergum VII ( +Figs. 146–147 +). Females are also characterised by the bright red and black intersegmental membrane between abdominal sternites I and II ( +Fig. 154 +). Eggs are distinctive by their very strongly sculptured capsule surface and comparatively smaller micropylar plate, which covers less than half of the capsule length ( +Figs. 155–156 +). + + + + + +Description: ♀ ( +Figs. 144–145 +, +394 +): + +Very small for the genus (body length including subgenital plate 92.0– +105.5 mm +), with a conspicuously shortened and strongly broadened mesothorax and comparatively short, dorsally unarmed legs. General colouration plain bright apple-green, the ventral body surface and basal half of subgenital plate dull green, sometimes with a slight whitish hue. Lateral margins of meso- and metasternum white and a longitudinal white stripe along the ventral surface of the lateral margins of the abdominal tergites. Points of the two large spines on the vertex, as well as all larger tubercles of the pro- and mesonotum and the row of spines on the meso- and metapleurae dark pink; +anterior +half of mesopleurae dark pink as well. Bases of dorsal thoracal tubercles and spines yellow. Antennae dark pink except for the two basal segments which are blackish with pale outer margins, and a few pale annulations in the apical 1/3. Tegmina and alae of same colouration as body. Tarsi and subgenital plate becoming pale brown towards the apex. Eyes creamish mid brown. + + +Head: Vertex strongly convex and armed with two very prominent, blunt spines; the dextral one larger ( +Fig. 148 +). A few minute granules are present posterior of these and a small pair of rounded granules on the frons. Eyes slightly elongate-oval, convex and of moderate size; their length contained about 2.6x in that of cheeks. Between the bases of the antennae with a fairly decided, slightly curved and transverse depression. Antennae reaching about half way along median segment; with 37 segments. Scapus dorsoventrally flattened, almost +3x +longer than wide and gently narrowed towards the base. Pedicellus cylindrical and about 2/5 the length of scapus. + + + +FIGURES 144–147. + +Diapherodes martinicensis +Lelong & Langlois, 2005 + +. +144. +♀ HT: Martinique, trace Duclos (dorsal view) [MNHN]; +145. +♀: captive reared from Martinique [coll. FH, No. 0750-1]; +146. +♂: captive reared from Martinique [coll. FH, No. 0750-8]; +147. +♂: captive reared from Martinique [coll. FH, No. 0750-5]. + + + + +FIGURES 148–156. + +Diapherodes martinicensis +Lelong & Langlois, 2005 + +. +148. +♀ head and pronotum [coll. FH, No. 0750-3]; +149 +. ♂ head and pronotum [coll. FH, No. 0750-5]; +150. +♀: apex of abdomen (lateral view) [coll. FH, No. 0750-3]; +151. +♀: apex of abdomen (dorsal view) [coll. FH, No. 0750-3]; +152. +♂: apex of abdomen (lateral view) [coll. FH, No. 0750-5]; +153. +♂: apex of abdomen (dorsal view) [coll. FH, No. 0750-5]; +154. +Metasternum and abdominal sterna I–II of ♀ showing the colourful inter-segmental membrane [coll. FH, No. 0750-3]; +155. +Egg (dorsal view) [coll. FH, No. 0750-E]; +156. +Egg (lateral view) [coll. FH, No. 0750-E]. + + + +Thorax: Pronotum shorter and about as broad as the head; roughly 1.3x wider than long. In front of the very prominent transverse median depression armed with a pair of very large, blunt spines; posterior half set with a few minute granules ( +Fig. 148 +). Mesothorax short, only about 1.3x longer than head and pronotum combined, decidedly constricted anteriorly and strongly broadened towards the posterior; posterior margin almost +4x +broader than +anterior +margin ( +Fig. 144 +). Mesonotum sparsely set with minute granules which slightly increase in size towards the +anterior +, otherwise dorsally armed with two pairs of prominent, blunt spines close to +anterior +margin and a further pair of similarly sized spines just before the middle ( +Fig. 148 +). Metanotum unarmed, about half the length of mesonotum and slightly wider than long. Spines of the meso- and metapleurae more acute than dorsal thoracal armature; mesopleurae with 12–13, metapleurae with 10–11 spines. Tegmina rather small and reaching about ¾ the way along metanotum (length 5.5–7.0 mm), posterior margin slightly angulate; not overlapping. Alae very small and projecting underneath tegmina by about 2.2–3.0 mm. + + +Abdomen: Median segment slightly longer than metanotum and roughly trapezoidal with the +anterior +margin narrowed. Segments II–VI slightly increasing in length and gradually narrowing, II about +2x +wider than long, VI 1.25x longer than wide. VII narrowest and about as long as VI, almost parallel-sided or with the posterolateral portions somewhat deflexed and forming a small, rounded lobe ( +Fig. 151 +). Tergites II–VII all with a faint, slightly curved longitudinal carina laterally. Intersegmental membrane between abdominal sternites I and II bright red and black ( +Fig. 154 +). Sternites II–VII with a blunt lateral longitudinal carina. Praeopercular organ formed by an elongate, keel-shaped swelling near posterior margin of sternum VII ( +Fig. 349 +). Tergum VIII slightly shorter and narrower than VII and widened towards the posterior; decidedly more convex than previous. IX less than half the length of VIII, slightly narrowed towards the posterior and very faintly keeled. Anal segment gently narrowed, posterior margin roundly angular and dorsally with a faint, longitudinal median keel. Epiproct small, broad and very slightly projecting underneath anal segment ( +Fig. 151 +). Subgenital plate long and considerably narrowed towards a slender and pointed tip; projecting over apex of abdomen by almost the combined length of tergites VIII–X ( +Figs. 150–151 +). + +Legs: All short, moderately broad and entirely unarmed, except for 4–5 minute spines on the two outer ventral carinae of the meso- and metafemora; these decrease in size towards the base. Profemora slightly longer than mesothorax and metatibiae slightly projecting over posterior margin of abdominal tergum V. Tarsi about half the length of corresponding tibia. Basitarsi indistinctly longer than second tarsomere. + + +♂ ( +Figs. 146–147 +, +395 +). + +Small (body length 64.0– +81.5 mm +) and moderately slender for the genus, with very long alae ( +43.5 mm +) and a comparatively short, dorsally sparsely spinose mesothorax. General colouration of head and body pale yellowish brown; ventral body segments whitish. Posterior half of poculum pale cream. Tegmina and costal region of alae creamish mid brown, the tegmina with a broad, longitudinal white stripe along the +anterior +margin and the central hump marked with dull pink. Anal region of alae pale translucent orange. Femora pale green basally and gradually becoming mid brown towards the apex (with a slight dull pink hue ventrally); tibiae entirely pale green with only the apex slightly brownish. Tarsi pale brown but becoming decidedly darker towards the apex. Cephalad pair of spines and all larger spines and tubercles of the thorax tipped with black. Antennae pale brown with the basal portion slightly reddish and the two basal segments very dark brown; a few dark brown annulations close to the apex. Eyes dark reddish brown. + + +Head: Generally as in ♀♀. Vertex strongly convex and smooth except for two prominent, blunt but slender cephalad spines ( +Fig. 149 +). Eyes large, very slightly oval and projecting hemispherically; their length contained less than +2x +in that of cheeks. Antennae reaching about half way along abdominal tergum III, otherwise as in ♀♀. + + +Thorax: Pronotum roughly quadrate and about as long and broad as head. Transverse median depression very prominent, almost straight and reaching lateral margins of segment. +Anterior +half with a pair of prominent blunt spines and posterior half with a pair of low tubercles ( +Fig. 149 +). Mesothorax short, just 1.5x longer than head and pronotum combined; mesonotum about +4x +longer than wide. Dorsal surface with a few minute granules and six distinct, blunt paired spines; two pairs close to +anterior +margin ( +Fig. 149 +) and a further pair slightly before the mid of segment. Lateral margins with a longitudinal row a small greenish tubercles. Meso- and metapleurae each with a longitudinal row of minute granules. Meso- and metasternum sparingly granulose. Tegmina reaching to posterior margin of metanotum. Alae at least reaching to posterior margin of abdominal tergum VII ( +Figs. 152–153 +). + + +Abdomen: Tergum VII with a distinct, rounded posterolateral lobe, which projects by about ¼ of the body width ( +Fig. 153 +). Tergites VIII–X very indistinctly broader than previous segments, VIII about ¾ the length of +VII and IX 2 +/3 the length of VIII. Anal segment gently narrowed towards the apex with the posterior margin broadly rounded ( +Fig. 153 +). Cerci slender and narrowing towards a blunt apex. Vomer with a fairly small base and a very long, gradually narrowing and acutely pointed apical hook ( +Fig. 369 +). Poculum strongly convex and conical basally, just slightly projecting over posterior margin of tergum IX (Fig. +Fig. 152 +); the posterior margin very broadly rounded. + +Legs: All of moderate length, profemora almost as long as pro- and mesonotum combined, metatibiae reaching about halfway along abdominal tergum VI. Posterodorsal carina of meso- and metafemora very slightly elevated and rounded sub-basally. Both outer ventral carinae of meso- and metafemora with 2–3 sub-apical spines; a few more minute spines are present in the median section of the posteroventral carina of the mesofemora. Remaining carinae unarmed. Tarsi elongate, about half the length of corresponding tibia. Basitarsi about 1.5x longer than second tarsomere. + + +Egg ( +Figs. 155–156 +): + +Rather small (capsule length +4.3–4.8 mm +), capsule 1.7x longer than wide. Polar area decidedly impressed if seen in lateral aspect. Capsule surface irregularly covered with prominently raised structures, these crater-like and with several distinct circular pits dorsally. Micropylar plate small, its length contained about 2.5x in that of capsule. Central portion of micropylar plate with two irregularly raised ridges, which begin at the micropylar cup and converge towards the +anterior +, where they terminate about +0.4 mm +off the +anterior +end of plate. Micropylar cup distinct. Operculum in the central portion with numerous irregular granules and tubercles; centre slightly lowered. General colour pale to dark brown. Outer margin of micropylar plate and micropylar cup mid brown. + +Measurements [mm]: Length 4.3–4.8, length (including operculum) 4.5–5.0 width 2.5–2.7, height 2.7–2.9, length of micropylar plate 1.7–1.8. + + + +Comments: +Lelong & Langlois (2005) described + +Diapherodes martinicensis + +from three ♀♀ and one ♂ and provided REM-photographs of the eggs. According to the small number of known specimens, + +D. martinicensis + +appears to be rare. Lelong & Langlois (2005: 264) reported this species to be apparently uncommon and to feed on guava ( + +Psidium guajava + +, +Myrtaceae +) and + +Coccoloba + +sp. ( +Polygonaceae +) in the wild. Only one ♀ was found during extensive collections conducted by these authors in several localities throughout +Martinique +. + + +Only two ♀♀ were collected by Christian Bouladou Dupré ( +Martinique +) on several occasions during 2011. The specimens were kept alive in captivity in +Martinique +and accepted + +Acacia muricata +(Fabaceae) + +, + +Tapura latifolia +(Dichapetalaceae) + +, +Pimenta racemosa +( +Myrtaceae +), + +Ocotea coriacea +(Lauraceae) + +and Avocado ( + +Persea americana + +, +Lauraceae +), hence at least some of these are likely to represent native host plants. Eggs were sent to Bruno Kneubühler ( +Switzerland +), who first successfully reared + +D. martinicensis + +in Europe. In captivity hawthorn ( + +Pyracantha coccinea + +, +Rosaceae +), salal ( + +Gaultheria shallon + +, +Ericaceae +), oak ( + +Quercus robur + +, +Fagaceae +) and dog rose ( + +Rosa canina + +, +Rosaceae +) are accepted as alternative food plants. Females produce an average of three eggs per day, which are simply flicked away by an abrupt movement of the abdomen. Eggs take some 4–5 months to hatch at temperatures of 20–25°C and nymphs reach maturity in 3–4 months. If disturbed, adult ♂♂ will readily flash their wings and are capable of short active flights. Females will either drop to the ground or pinch with their hind legs, to expose the bright red and black coloured intersegmental membrane between the abdominal sternites I and II ( +Fig. 154 +). + + + + + +Distribution ( +Fig. 381 +): + +Martinique +(Trace Duclos [MNHN]; Balata [coll. H. Griffon] & Morne-Rouge [MNHN]). Endemic. + + + + +Number of specimens examined: +40 + + + +TABLE 15. +Measurements of + +Diapherodes martinicensis +Lelong & Langlois, 2005 + +[mm] + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
♀♀, HT & PT*♂, PT [coll. Pinchon]*♀♀ [coll. FH]♂♂ [coll. FH]
Body (incl. sg. pl.) Body92.0–97.0 -- 64.092.0–105.5 87.0–97.3- 68.0–81.5
Pronotum Mesonotum4.0 12.5–13.02.5 9.53.9–4.1 13.0–14.02.2–2.7 8.9–10.6
Metanotum Median segment6.0–8.0 6.5–8.512.0** -5.3–5.8 7.0–7.55.3–5.9 6.0–7.0
Tegmina Alae Profemora7.0 - 13.0–15.011.5 43.5 11.55.0–6.2 2.2–3.0 11.8–14.79.0–11.0 40.5–50.0 10.5–12.6
Mesofemora12.0–14.511.010.6–12.59.4–11.0
+
+ +......continued on the next page +* according to Lelong & Langlois (2005: 266) + + + +TABLE 15. +(Continued) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
♀♀, HT & PT*♂, PT [coll. Pinchon]*♀♀ [coll. FH]♂♂ [coll. FH]
Metafemora17.5–21.015.015.8–19.012.5–15.8
Protibiae--10.3–12.69.9–11.5
Mesotibiae--9.8–11.38.1–9.9
Metatibiae--14.6–16.012.0–14.0
Antennae29.5–30.037.531.5–36.036.5–44.0
+
+** including median segment +
+
+
\ No newline at end of file diff --git a/data/38/7F/30/387F3068D379FFD9FF27EB6E25F31DF3.xml b/data/38/7F/30/387F3068D379FFD9FF27EB6E25F31DF3.xml new file mode 100644 index 00000000000..b4bd0d69fe4 --- /dev/null +++ b/data/38/7F/30/387F3068D379FFD9FF27EB6E25F31DF3.xml @@ -0,0 +1,666 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Diapherodes achalus +(Rehn, 1904) + +n. comb. + + + + +( +Figs. 157–166 +, +350 +, +370 +, +382–383 +) + + + + + +Aplopus achalus +Rehn, 1904: 68 + +. +HT +, ♂: Adjuntas P.R. +12 Apr. +0 0, C.W. Richmond Collector, Cat. no. + +Aplopus achalus +Rehn + + + + + +Type +, +Type +No. 7344 +U.S. +N.M. [ +USNM +, No. 7344]. + +Wetmore, 1916: 58. +Wolcott, 1923: 23. +Wolcott, 1936: 35. +Wolcott, 1948: 50. +Wolcott, 1951: 50. + + +Diapherodes achalus +, Van de Bussche +et al. +, 1988: 422 + +. + +Haplopus achalus +, Kirby, 1904a: 363 + +. + +Otte & Brock, 2005: 150. + + +Diapherodes achalus +, Moxey, 1972: 90 + +(in litt.). + +Diapherodes longiscapha +Redtenbacher, 1908: 435 + +. +LT +(by present designation), ♀: Porto-Rico, Antilles, Mr. H. de Saussure, + + + +Diapherodes longiscapha +REDT +. + +[ +MHNG +]; +PLT +, ♀: 141, Portorico Coll. Krug, + +Diapherodes longiscapha +Br. Brunner + +det, + + + + +Type +[MNHU] +n. syn. + +Wolcott, 1923: 23. +Wolcott, 1936: 35. +Wolcott, 1948: 50. +Wolcott, 1951: 50. +Zompro & Brock, 2003: 16. +Otte & Brock, 2005: 121. + + +Diapherodes gigantea +, Wolcott, 1923: 23 + +. ( +Misidentification +—not + +Mantis gigantea +Gmélin, 1789 + +) Wolcott, 1936: 35. + +Wolcott, 1948: 50. +Wolcott, 1951: 50. + + +Diapherodes krugii +, Wolcott, 1923: 23 + +. (Nomen nudum) Wolcott, 1936: 35. + + + + + +Further material [16 ♂♂, 15 ♀♀, 1 nymph, +1 egg +]: + + + +PUERTO RICO +: + + +1 ♂ +: +Puerto Rico +: Parador, Casa Grande, nr. Utuado, +16-III-1990 +, at light, R.E. & K.E. Wooruff [ +FSCA +]; 1 ♀: Barranguitas, P.R., +June 1959 +, coll. L.F. Martorell [ +USNM +]; 1 ♀ (in Ryker mount): From +Porto Rico +Exp. Stat. […] Nov. 19.1913; + +Diapherodes longiscapha +Redt. + +♀ A.n.c. [ +USNM +]; 1 ♀: Road S.G. to Mariacao, 18K6M side road, Beating from Tree, +Feb. 13 +,'61, A.M. Nadler; P.R. Road from Maricao-Sabana Grande km 18.6, Beating tree, +Feb. 13 +,'61, A.M. Nadler; + +Diapherodes longiscapha +Redt. + +♀, det. A.B. Gurney 1961 [ +USNM +]; +1 ♂ +: P.R. +ACC +.NO. 69–50, Cayey, P.R., Sept. 26,1950; G.N. Wolcott & L.F. Martorell Collectors; +USMNH +; w0150; + +Diapherodes achalus +(Rehn) + +det. CF Moxey 1972 [ +USNM +]; +1 ♂ +: Utuado, P.R., +Nov. 1948 +, Coll: E. Boneta; w0152; +USMNH +; + +Diapherodes achalus +(Rehn) + +det. CF Moxey 1972 [ +USNM +]; +1 ♂ +: Caguas, P.R., Jan. 8.1912, in bird stomach. Biol. Survey.; + +Aplopus achalus +Rehn A. + +n.c [ +USNM +]; 2 ♂♂: Barranquitas, P.R., +Nov. 20 1948 +, Coll. S. Rodriguez [ +USNM +]; +1 ♂ +: Mayaguez, P.R., +1/14/47 +, C. Feyre R. [ +USNM +]; +1 ♂ +: Mayaguez, P.R., +1-19-1930 +, Coll. E. +Rosa +[ +USNM +]; +1 ♂ +: Ponce, P.R., +X-20 1947 +[ +USNM +]; 1 ♀: Juyuya PR, +VIII-14- 54 +, H F Winters, PR-1278; Toro Negro Ar, Carribean Nat. Forest, Lot 45-19676 [ +ANSP +]; 1 ♀ (valde defectum): Yauco, P.R., +June 1945 +, Coll: [ +USNM +]; 2 ♀♀: Rio Piedras, P.R., +IV-2-1944 +, Coll: R. Casas [ +USNM +]; 1 ♀: Barranquitas, P.R., +Oct. 10 1948 +, Coll. S. Rodriguez [ +USNM +]; 1 ♀: Maricao, P.R., +Nov. 20 1990 +, Coll: Iv. Nazario [ +USNM +]; 1 ♀: Aibonito, P.R., +8-9-33 +, R.G. Oakley; on leaf + +Inga vera + +; San José No. 4630; wO143 [ +ANSP +]; 1 ♀: El Yunque Mountains, Luquillo, P.R., +June 1935 +; cdl. L. F. Martore, Host: on weeds, Acc#: 29–35; wO144 [ +ANSP +]; 1 ♀: Jayuya, PR, +Aug. 23–45 +, H F Winters, PR No. 472; on + +Cinchona ledgeriana + +; Lot No. 56-1971; wO147 [ +ANSP +]; +1 ♂ +: Jayuya, P.R., +Aug. 23–45 +, H F Winters, PR No. 470; on + +Cinchona ledgeriana + +; wO151 [ +ANSP +]; +1 ♂ +: Mayaguez, PR; wO149 [ +ANSP +]; 1 ♀ (penultimate instar): Yauco, P.R., +II.1934 +, Cdi J. +Matini +; wO146 [ +ANSP +]; 1 ♀: Mayaguez, P. R,. +3. Oct. 1938 +; J. A. Ramos Collector [ +ANSP +]; +1 ♂ +: Mayaguez, P. R., +21 Oct. 1937 +, Coll.: R. del Moral [ +ANSP +]; +1 ♂ +: Aibonito, P. R., +II-16-1935 +, Coll. J. Martinez [ +ANSP +]; 1 ♀, +1 egg +(ex ovipositor): +Porto Rico +, Mayaguez, +5.7.1906 +, C. Gaggo leg.; +PHA +12, Zoologisches Museum Hamburg [ +ZMUH +]; 1 ♀: Mayaguez, +Porto Rico +, C. Gaggo leg. +5.VII.1906 +, ded. +3.IX.1906 +; +PHA +11, Zoologisches Museum Hamburg [ +ZMUH +]; +1 ♂ +: +Puerto Rico +, Maricao, +13.10.2009 +, leg. Mel J. Rivera [coll. OC]. + + +NO +DATA +: + + +1 ♂ +: F. Sein Collector; + +Aplopus jamaicensis +(Drury) + +A.n.c. [ +USNM +]. + + + + +Diagnosis: +Well characterized and distinguished from the two other species of the + +jamaicensis + +species-group by the elongate head, just gently rounded and almost unarmed vertex ( +Figs. 159–160 +), entirely unarmed mesothorax ( +Figs. 157–158 +) and having only two apical spines on the medioventral carina of the meso- and metafemora in both sexes. ♂♂ furthermore differ by the bold brown longitudinal median stripe on the tegmina ( +Fig. 158 +) and brown cheeks ( +Fig. 160 +). The characteristic eggs are unique within the entire genus by having a hollow polar area and a prominent conical swelling on the operculum ( +Figs. 165–166 +). + + + + +Description: +The colouration is described from several photos of live specimens taken at Maricao in +Puerto Rico +by Mel J. Rivera ( +Figs. 374–375 +). + + + +♀ ( +Fig. 157 +, +382 +). + +Fairly small (body length including subgenital plate 92.0–116.0 mm) and rather massive member of the + +jamaicensis + +species-group with a moderately widened mesothorax and abdominal segment VII. Colour bright apple green, the meso- and metapleurae ochre with a white longitudinal stripe along lower margin. Ventral body surface mostly whitish. Tegmina and costal region of alae bright green with the +anterior +margin darker in colour. Anal region of alae dull pink to violet. Antennae dark ochre dorsally and blackish brown ventrally. Eyes pale ochre. + + +Head: Elongate, ovate and 1.3x longer than wide, the vertex very gently convex and smooth except for a very faint pair of cephalad tubercles; the sinistral very faint ( +Fig. 159 +). Eyes rather small, circular and their length contained a little more than +3x +in that of cheeks. Antennae broken in all specimens at hand but at least reaching to metanotum. Scapus dorsoventrally compressed, constricted basally with the outer lateral margin gently rounded, 2.3x longer than wide. Pedicellus oval in cross-section about 2/3 the length of scapus. + + +Thorax: Pronotum considerably shorter and narrower than head, hardly longer than wide and gently narrowing towards the posterior. Transverse median depression deep but very short and curved. Surface unarmed except for a pair of small tubercles just in front and behind the median sulcus ( +Fig. 159 +). Mesothorax about 1.6x longer than head and pronotum combined, constricted +in anterior +portion and then gradually widened towards the posterior; posterior margin more than +3x +wider than +anterior +margin. Mesonotum very slightly tectiform longitudinally and widened towards the middle, then roughly parallel-sided; surface smooth except for a few scattered small tubercles, in particular in the +anterior +portion. Mesopleurae with a marginal row of spiniform tubercles or short spines; metapleurae armed with a row of about eight short spines. Pro-, meso- and metasternum smooth; the mesosternum occasionally with a small pair of granules posteriorly. Tegmina oval, reaching to posterior margin of metanotum and with the central protuberance moderate. Alae roughly equal in length to tegmina and reaching about half way along median segment. + + + +FIGURES 157–160. + +Diapherodes achalus +(Rehn, 1904) + +. +157. +♀: Puerto Rico, Mayaguez [ANSP]; +158. +♂: Puerto Rico, Parador Casa Grande [FSCA]; +159. +♀ head and pronotum: Puerto Rico, Mayaguez [ANSP]; +160. +♂ head and pronotum Puerto Rico, Parador Casa Grande [FSCA]. + + + +Abdomen: Median segment slightly longer than wide and very gently widening towards the posterior; smooth. Abdomen strongly swollen sub-basally with segment II widening, IV narrowing and III widest. II–IV transverse and III almost 1.5 wider than long. V–VIII longer than wide, VII moderately expanded and with the lateral margins rounded ( +Fig. 162 +). Tergites II–IV smooth, V–VII with four roughly parallel, longitudinal carinae which are most decided on VII ( +Fig. 162 +). Sternites II–VII smooth except for a fine carina along lateral margins. Praeopercular organ formed by a brown tubercle close to posterior margin of sternum VII ( +Fig. 350 +). Tergites VIII–X narrower than previous segments and roughly of uniform width. VIII about ¾ the length of VII and very slightly constricted medially, about 1.2x longer than wide; IX indistinctly longer than wide. Anal segment about equal in length to IX, with a slight longitudinal median carina in basal portion and flattened towards the posterior; posterior margin rounded and with a very small and shallow median indentation ( +Fig. 162 +). Epiproct small and semi-circular with a keel dorsally ( +Fig. 162 +). Cerci very small, round in cross-section and tapered towards a pointed apex. Subgenital plate elongate, lanceolate, longitudinally keeled and variable in length; projecting over apex of abdomen by more than the combined length of tergites IX–X ( +Figs. 161–162 +). + +Legs: Profemora slightly shorter, mesofemora about ¾ the length of mesothorax and metafemora reaching about half way along abdominal segment IV. Medioventral carina of all femora with two rather small spines in apical portion. Posteroventral carina of meso- and metafemora with one, the anteroventral carina with two distinct, black-tipped sub-apical spines. Basitarsi no longer than following two tarsomeres combined. + + +♂ ( +Figs. 158 +, +383 +). + +Small (body length 60.0–74.0 mm) and fairly robust for the + +jamaicensis + +-group with a very characteristic colouration, body surface glabrous, with very long alae (36.8–42.0 mm). General colour bright green, washed with brown, the lateral surfaces of the head, entire pronotum, mesonotum, mesopleurae, posterior portion of metapleurae and bases of all femora ochraceous. Abdominal tergites V–X green laterally, yellow dorsally and V–IX with a mid to dark brown longitudinal median stripe ( +Fig. 321 +). Ventral surface of abdomen with a whitish wash. Head bright green with the cheeks ochraceous brown and two bold, washed yellow markings between the eyes ( +Fig. 160 +). +Anterior +margin of tegmina and basal portion of the same region of the alae white, tegmina with a further broad brown longitudinal stripe, the innermost portion green with darker green veins and basal portion yellow ( +Fig. 158 +); costal region of alae plain green with dark green longitudinal veins, the anal region very pale and translucent pink. Eyes mid to dark brown. Antennae greyish ochre. Ventral sub-apical spines of the meso- and metafemora black. + + +Head: Ovate and only about 1.2x wider than long, otherwise generally as in ♀♀; cephalad tubercles very faint ( +Fig. 160 +). Eyes of moderate size and projecting hemispherically, their length contained less than +2x +in that of cheeks. Antennae projecting over posterior margin of abdominal segment II and moderately robust; with 36–37 antennomeres. Scapus oval in cross-section, roundly rectangular with the inner margin concave and about 1.3x longer than wide. Pedicellus cylindrical and about 2/3 the length of scapus. + + +Thorax: Pronotum slightly shorter and narrower than the head, with the +anterior +portion slightly broader than posterior portion; median transverse depression distinct, gently curved and almost reaching lateral margin of segment. Surface smooth or with a very few minute granules ( +Fig. 160 +). Mesothorax 1.8x longer than head and pronotum combined; mesonotum at best with a few very obsolete granules anteriorly. Mesopleurae smooth, metapleurae with a few small granules. Meso- and metasternum smooth. Tegmina oval and with a rather longitudinal and acute central protuberance, roughly reaching to posterior margin of metanotum. Alae ± reaching to posterior margin of abdominal tergum VII ( +Fig. 158 +). + + +Abdomen: Median segment gently narrowed towards the posterior. Segments II–VI slightly decreasing in length and width, II 2.7x and VI only about +2x +longer than wide. elongate, cylindrical, parallel-sided and gradually decreasing in length. II 3.5x, VII 2.5x longer than wide. VII about equal in length to VI and very slightly widened posteriorly. Sternites II–VII smooth. Tergum VIII about 3/5 the length of VII, widened towards the posterior and slightly tectate. IX slightly shorter than VIII and very slightly narrowed towards the posterior. Anal segment about as long as IX with two longitudinal carinae dorsally, slightly constricted towards the posterior and the posterior margin sub-truncate with a shallow median emargination ( +Fig. 164 +). Vomer roughly triangular with a moderately long terminal hook ( +Fig. 370 +). Cerci about 2/3 the length of anal segment, rather slender, cylindrical and very slightly in-curving with the apex blunt. Poculum moderately convex, cymbiform and longitudinally carinate, the posterior margin rounded and with a narrow median emargination; very slightly projecting over posterior margin of tergum IX ( +Fig. 163 +). + +Legs: Shape and armature generally as in ♀♀. + + +Egg ( +Figs. 165–166 +): + +Medium sized (capsule length 5.0 mm), capsule about +2x +longer than wide and slightly higher than wide. Capsule surface srtrongly and irregularly sculptured with several raised swelling and an irregular swollen keel indicated, that surrounds the micropylar plate and posteriorly runs towards lateral surfaces of capsule. Another distinctly raised, blunt keel below micropylar plate, which almost reaches to the polar area. The polar area hollow, impressed and surrounded by an irregularly toothed rim. +Anterior +margin with an irregularly crown-like rim of tooth like and anteriorly directed swellings. Micropylar plate small, heart-shaped and its length contained about 3.5x in that of capsule. Central portion impressed but otherwise strongly swollen. Operculum sub-circular with a large, irregularly sculptured conical swelling in centre. General colour pale to mid ochraceous to reddish brown. + + + +FIGURES 161–166. + +Diapherodes achalus +(Rehn, 1904) + +. +161. +♀ apex of abdomen of synonym HT of + +D. longiscapha + +(lateral view) [MHNG]; +162. +♀ apex of abdomen of HT of synonym + +D. longiscapha + +(dorsal view) [MHNG]; +163. +♂ apex of ♂ abdomen (lateral view) [FSCA]; +164. +♂ apex of abdomen (dorsal view) [FSCA]; +165. +Egg: Puerto Rico, Mayaguez (dorsal view) [ZMUH]; +166. +Egg: Puerto Rico, Mayaguez (lateral view) [ZMUH]. + + +Measurements [mm]: Length 5.0, length (including operculum) 6.2 width 2.5, heigth 2.9, length of micropylar plate 1.3. + + + +Comments: +Moxey (1972: 10, in litt.) stated + +D. achalus + +to have been taken on + +Guarea ramiflora +(Meliaceae) + +and + +Inga vera +(Mimosaceae) + +which might both be part of its natural diet. Body lengths cited by Moxey (1972: 92, in litt.) are 61.0–74.0 mm for ♂♂ and 92.0–114.0 mm including the subgenital plate for ♀♀. + + + + +Distribution: +Puerto Rico +: Barranquitas [USNM]; Mayaquez [ANSP, ZMUH]; Maricao Forest [ANSP, coll. OC]; Yauco [ANSP]; between Maricao and Sabana Grande km 18.6 [USNM]; Cayey [USNM]; Adjuntas [ANSP, USNM]; Utuado [USNM]; Jayuya [ANSP]; Aibonito [ANSP]; Ponce [USNM]; Rio Piedras [USNM]; Caguas [USNM]; Naguabo, El Yunque Quadrangle, Naguabo [Van den Bussche +et al. +, 1988: 423] & Luquillo Experimental Forest, El Verde [ANSP]. Endemic. + + + + +Number of specimens examined: +35 + + + +TABL +16. + +Measurements of + +Diapherodes achalus +(Rehn, 1904) + + +n. comb. + +[mm] +......continued on the next page + +TABL +16. + +(Continued) + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D379FFDCFF27ECD9263619A9.xml b/data/38/7F/30/387F3068D379FFDCFF27ECD9263619A9.xml new file mode 100644 index 00000000000..16e6e6c107a --- /dev/null +++ b/data/38/7F/30/387F3068D379FFDCFF27ECD9263619A9.xml @@ -0,0 +1,96 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +5.4.2. The + +jamaicensis + +species-group + + + + + + +Characteristics: +The three known members of the + +jamaicensis + +species-group are restricted to the two Greater Antillean islands of +Jamaica +and +Puerto Rico +( +Fig. 375 +). They are of moderate size for the genus (body lengths: ♂♂ 60.0–94.0 mm, ♀♀ including subgenital plate 84.0– +164.5 mm +) with ♀♀ ranging from rather slender to moderately robust. Body surface of ♂♂ sub-glabrous to glabrous. Colouration of both sexes usually bright green (♀♀ more rarely brown or with brown markings). Pronotum without +anterior +spines; at best sparsely tuberculate. Mesonotum of ♂♂ entirely unarmed or with 2–6 paired +anterior +spines. Meso- and metasternum smooth (♂♂), mesosternum may have a few minute granules in ♀♀. Meso- and metapleurae of ♂♂ unarmed, of ♀♀ with a marginal row of granules or spiniform tubercles. Alae of ♀♀ ± as long as tegmina; anal region of both sexes plain pink to purple. Abdomen of ♀♀ broadened sub-basally with segment III broadest. Tergites IV–VII of ♀♀ ± decidedly multicarinate; VII ± strongly laterally expanded or with a triangular posterolateral lobe. Epiproct of ♀♀ large, triangular to shield-shaped and distinctly projecting over anal segment. All carinae of legs unarmed, except for spines on medioventral carina and sub-apical spines on the two outer ventral carinae of the meso- and metafemora. Dorsal carinae of meso- and metafemora may bear a ± tooth or lobe sub-apically. Eggs small to moderately sized (capsule length <5.0 mm), micropylar plate small and usually <1/3 the length of capsule. For a detailed comparison with the + +gigantea + +species-group see +Table 10 +. + + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D37CFFE1FF27EDD925801F45.xml b/data/38/7F/30/387F3068D37CFFE1FF27EDD925801F45.xml new file mode 100644 index 00000000000..da9b4eb39d5 --- /dev/null +++ b/data/38/7F/30/387F3068D37CFFE1FF27EDD925801F45.xml @@ -0,0 +1,1412 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Diapherodes jamaicensis +(Drury, 1773) + +n. comb. + + + + +( +Figs. 167–182 +, +351 +, +371 +, +375 +, +388–391 +) + + + + + +Mantis jamaicensis +Drury, 1773: 88 + +, pl. 49: 1 (♂). +HT +, ♂: +Jamaica +[not traced—believed lost]. Fabricius, 1787: 227. + +Olivier, 1792: 634. +Fabricius, 1793: 15. + + +Aplopus jamaicensis +, Rehn, 1903: 132 + +. + +Brock, 1998b: 33. +Otte & Brock, 2003: 302. + + +Cyphocrana jamaicensis +, St. Fargeau & Audinet-Serville, 1825: 445 + +. + + + +Diapherodes jamaicensis +, Moxey, 1972: 102 + +(in litt.). + + + +Haplopus jamaicensis +, Westwood, 1859: 86 + +. + +Kirby, 1904a: 363. +Redtenbacher, 1908: 430. +Otte & Brock, 2005: 151. + + +Phasma jamaicensis +, Fabricius, 1798: 188 + +. + + + +Phasma jamaicense +, St. Fargeau & Audinet-Serville, 1825: 101 + + + + +Phasma (Platycrana) jamaicensis +, Westwood, 1837: 99 + +, pl. 44: 1 (♂). + + + +Platycrana jamaicensis +, Gray, 1835: 38 + +. + + + +Mantis bispinosa +Fabricius, 1775: 274 + +. +LT +, ♂: “ +America +. Mus. Dom. Hunter” [specimen with wings open] [HMUG]; +PLT +, 2 ♂♂: same data as LT [HMUG]. [Synonymised by Redtenbacher, 1908: 430] + +Aplopus bispinosus +Brock, 1998c: 33 + +. [ +Lectotype +designation] Gmélin, 1789: 2054. + +Olivier, 1792: 633. + + +Mantis +2 spinosa + +, Fabricius, 1787: 227. + +Fabricius, 1793: 15. + + +Haplopus bispinosus +, Westwood, 1859: 87 + +. + +Kirby, 1904a: 430. +Otte & Brock, 2003: 303. + + +Phasma bispinosa +, Fabricius, 1798: 188 + +. + +Latreille, 1806: 87. + + +Phasma bispinosum +, Audinet-Serville, 1831: 58 + +. Gray, 1835: 24. + + + +Haplopus christopheri +Westwood, 1859: 84 + +, pl. 33: 4, 4a (♀). +LT +(by present designation), ♀: St. +Christopheri +, W. Indies, E. Shepard; + +Diapherodes christopheri +Westwood + +, p. 84, pl. 33 f4; Type—Westwood, + +Haplopus christopheri +, Cat Phasm. + + + + + +1859, p. 84, pl. +33 f. +4; +Type +Orth: 614 1/2, +Diapherodes christopheri +Westw., Hope Dept. Oxford [OXUM, No. 614]; +PLT +, ♀: St. Christopher + +, +1858 +, + +W. Indies, E. Shepard; +<emphasis id="82A25D6CD37FFFDAFD4AEEE127971D83" box="[762,1023,182,204]" italics="true" pageId="94" pageNumber="95">Diapherodes christopheri</emphasis> +Westwood + +, p. +84 +, pl. 33 f4; Cat Phasm. 1859, p. +84 +, pl. +33 f. +4; +Type +Orth: 614 2/2, +Diapherodes christopheri +Westw., + +Hope Dept. Oxford [OXUM, No. 614] +n. syn + +. + + + + +Diapherodes christopheri +, Kirby, 1904a: 462 + +. + +Redtenbacher, 1908: 434. +Moxey, 1972: 94 (in litt.). +Otte & Brock, 2005: 120. + + +Diapherodes glabricollis +Gray, 1835: 33 + +. +HT +, ♀: +Type +; + +Haplopus glabricollis +G.R. Gray + +,—?, + +glabricollis +Gray + +108, + +Diapherodes glabricollis +Gray + +, HT; BMNH(E) #844944 [NHMUK]. +n. syn. +Brock +et al. +, (in press) + + + +Haplopus glabricollis +, Westwood, 1859: 88 + +. + +Kirby, 1904a: 364. +Redtenbacher, 1908: 430. +Otte & Brock, 2005: 151. + + +Diapherodes glabricollis +, Burmeister, 1838: 575 + +. + + + +Haplopus murinus +Redtenbacher, 1908: 429 + +. +LT +, ♀ (by present designation): Coll. Br. v. W., +Jamaika +, Burr; Det. Br. v. W., + +Haplopus murinus + +; 25.068; Stony Hill, +Jamaica +, +July 29/93 +, Hwm; +Lectotypus +, + +Haplopus murinus +Redt., P.D. Brock + +[NHMW, No. 834]; +PLT +, ♀: Cuming, Jan., +Jamaica +, Burr; det. Br. v. W. + +Haplopus murinus + +, +Paralectotypus +, + +Haplopus murinus +Redt., P.D. Brock + +[NHMW, No. 834]. +n. syn. + + + +Aplopus murinus +, Brock, 1998a: 44 + +. + + + +Haplopus murinus +, Otte & Brock, 2005: 152 + +. + + + +Diapherodes murinus +, Moxey, 1972: 103 + +(in litt.). + + + +Diapherodes pulverulentus +Gray, 1835: 34 + +. +HT +, ♀: + +Diapherodes pulverulentus +Gray + +; + +pulverulentus +Gray + +III + +Haplopus pulverulentus +G. R. Gray + +;—? + +Diapherodes pulverulentus +Gray + +HT; BMNH(E) #844949 [NHMUK]. +n. syn. +Brock +et al., +(in press) + + + +Haplopus pulverulentus +, Kirby, 1904a: 364 + +. + +Redtenbacher, 1908: 431. + + +Otte & Brock, 2005: 152. + + + +Further material [70 +♂♂, +47 +♀♀, +7 nymphs, eggs]: + + +JAMAICA +: + + +1 ♀ [brown form]: Kingston, +Jamaica +, C.R. Orcutt.; +USMNH +; w0214; + +Diapherodes jamaicensis +(Drury) + +det. C.F. Moxey 1972 [ +USNM +]; 1 ♀ [brown form]: Jam., Quick Step. nr. Aberdee, +VIII.8. +'41, W.G. Lynn; USDMNH; w0211; + +Diapherodes jamaicensis +(Drury) + +det. C.F. Moxey 1972 [ +USNM +]; 1 ♀: +Jamaica +, Recd. 1928, C.R. Orcutt; +USMNH +; w0210; + +Diapherodes jamaicensis +(Drury) + +det. C.F. Moxey 1972 [ +USNM +]; +1 ♂ +: Fellowship Rio Grande, July 27,1962, Farr, O. & R. Flint, +Jamaica +, Portland Parish; +USMNH +; + +Diapherodes jamaicensis +(Drury) + +det. C.F. Moxey 1972 [ +USNM +]; +1 ♂ +: Bath, +Jamaica +, +July 1902 +; + +Diapherodes jamaicensis +(Drury) + +det. C.F. Moxey 1972 [ +USNM +]; 3 ♂♂, 1 ♀: Coll. Br. v. W., +Jamaica +; det. Br. v. W., + +Haplopus jamaicensis + +[ +NHMW +, No. 833]; 1 ♀: Coll. Br. v. W., +Jamaica +; det. Br. v. W., + +Haplopus jamaicensis + +; + +Haplopus jamaicensis + +[18]93 [ +NHMW +, No. 833]; +1 ♂ +, 1 ♀: Cumming, Jan. 847; Mus. Caes. Vind., +Jamaika +, Cumming leg.; det. Redtenb. + +Haplopus jamaicensis + +[ +NHMW +, No. 833]; +1 ♂ +: Coll. Br. v. W., +Jamaica +; det. Br. v. W., + +Haplopus jamaicensis + +; 22.767; + +Haplopus jamaicensis +Drury + +, +Jamaica +[ +NHMW +, No. 833]; +1 ♂ +: +Jamaica +; 45 110 [ +NHMUK +]; +1 ♂ +: +Jamaica +; 46 84; + +Haplopus jamaicensis +(Drury) + +, +Jamaica +[ +NHMUK +]; +1 ♂ +: +Jamaica +; 46 84 [ +NHMUK +]; +1 ♂ +, 1 ♀: +Jamaica +; 61 63 [ +NHMUK +]; +1 ♂ +: +Jamaica +, Mandeville, L. J. Bertram, B. M. 1923-574 [ +NHMUK +]; 1 nymph (n1): +Jamaica +96-220 [ +NHMUK +]; 1 ♀: +Jamaica +, Dr. Leon, Brit. Mus. 1922-162, + +Haplopus murinus +Redt., Det. B. Uvarov + +♀ [ +NHMUK +]; +1 ♂ +: 54 76; +Brasil +[ +NHMUK +]; 1 ♀: 34J, +Jamaica +, + +Haplopus + +an foem. + +Jamaicensis + +?, +Jamaica +[ +NHMUK +]; 1 ♀: +Jamaica +: Blaudeville, Da Careret College, +26.V.1969 +, K. Stanton, B. M. 1969-506, + +Diapherodes jamaicensis +(Drury) + +det. Moxey 1972 [ +NHMUK +]; +1 ♂ +: +Jamaica +: Portland, Parrish, Millbank, +4-VIII-1985 +, C.B. & H.V. Weems Jr., G.B. Edwards [ +FSCA +]; 1 ♀: M. Delfosse, +Jamaique +, ♀ Elevage +02/04/2005 +[ +MNHN +]; 1 ♀: M. Delfosse, +Jamaique +, ♀ Elevage +10/04/ 2005 +[ +MNHN +]; +1 ♂ +: + +Haplopus jamaicensis +T. Jourdan + +♂ Elevage 06/2010 [ +MNHN +]; 5 ♂♂, 6 ♀♀, 3 ♀♀ (nymphs), +1 ♂ +(nymph), eggs: ex Zucht: F. Hennemann, urspr. +Jamaika +, +2000–2002 +[coll. FH, No’s 0428-1 to 11, 14 to 16, E & MP]; Right tegmen and ala of ♂: ex Zucht: F. Hennemann, urspr. +Jamaika +, +2000–2002 +[coll. FH, No’s 0428-12 and 13]; 5 ♀♀, 7 ♂♂, 2 ♀♀ (penultimate instar), 1 ♀ (n5), eggs: ex Zucht F. Hennemann 2008/09, Herkunft: +Jamaica +, Blue Mts., leg. T. & P. James (PSG No. 214) [coll. FH, No’s 0428-17 to 30 & 33]; 2 ♀♀, 6 ♂♂: ex Zucht F. Hennemann 2009, Herkunft: +Jamaica +, Blue Mts., leg. T. & P. James (PSG No. 214) [coll. FH, No’s 0428-31, 32 & 34-39]; 2 ♀♀, 2 ♂♂: +Jamaica +, F. Klages; Coll. W. +Holland +; A.N.S.P., Ex Carn. Mus., Bruner Cln. [ +ANSP +]; +1 ♂ +: +Jamaica +; wO222 [ +ANSP +]; +1 ♂ +: Jasmaica; wO217 [ +ANSP +]; 30 ♂♂, 18 ♀♀, eggs: ex Zucht O. Conle, Herkunft: +Jamaika +[coll. OC]. + + +NO / ERRONEOUS +DATA +: + + +2 ♀♀: Africa, J. E. Teede, B. W. 1928-311 [ +NHMUK +]; +1 ♂ +: + +bispinosum +Fab. + +, 106 [ +NHMUK +]; +1 ♂ +: +Brazil +, 54, 76; + +Haplopus bispinosus +(Fabr.) + +Brazil +[ +NHMUK +]; +1 ♂ +: +Brazil +, 54, 70 [ +NHMUK +]. + + + + +FIGURES 167–170. + +Diapherodes jamaicensis +(Drury, 1773) + +. +167. +♀: captive reared from Jamaica (typical green specimen with a short subgenital plate) [coll. FH, No. 0428-20]; +168. +♀: captive reared from Jamaica (green specimen with a brownish wash and a very short subgenital plate) [coll. FH, No. 0428-19]; +169. +♀: captive reared from Jamaica (typical green specimen with a long subgenital plate and strongly developed leg-armature) [coll. FH, No. 0428-17]; +170. +♀, PLT of synonym + +Haplopus murinus +Redtenbacher, 1908 + +: Jamaica (brown colour-form) [NHMW, No. 834]. + + + + +Diagnosis: +This species differs from the other two representatives of the + +jamaicensis + +species-group by the slender body of ♀♀ in particular, which makes it resemble members of the genus + +Haplopus +Burmeister, 1838 + +, and short alae of ♂♂, which merely reach to abdominal segment VI (VII in the other two species). From the Puerto Rican + +D. achalus +(Rehn, 1904) + +♀♀ furthermore differ by the spines and tubercles of the mesonotum and prominent cephalad horns, while they are at once distinguished from the second Jamaican species + +D. laevicollis +Redtenbacher, 1908 + +by the just gently widened mesothorax, shorter alae, which merely reach half way along the median segment, and not broadly rounded abdominal tergum VII. Males differ from those of + +D. achalus + +by the plain green tegmina and +anterior +spines of the mesonotum and from + +D. laevicollis + +by the dorsally brown scapus and pedicellus, more sender body and much shorter terminal hook of the vomer ( +Fig. 371 +). + + + + + +Description: ♀ ( +Figs. 167–170 +, +390–391 +). + +Medium-sized to large (body length including subgenital plate 104.0– +164.5 mm +) and moderately slender for the genus with a rather slender and almost parallel-sided abdomen and just slightly widened mesothorax. Colouration very variable and occurring in a green and brown colour-form, which are here described separately i) +Green form +( +Figs. 167, 169 +, +390 +): Colour bright apple green, the ventral body surface dull green. Lateral margins of mesonotum ochre, meso- and metapleurae ochre with a white longitudinal stripe along lower margin; membranes along lateral margins of the abdomen whitish. Tegmina and costal region of alae bright green, the +anterior +margin of tegmina brown and interiorly bordered by an obscure yellow longitudinal stripe; basal portion of alae with a bold brown marking. Anal region of alae plain pink ( +Figs. 167–168 +). Antennae pale brown dorsally, black ventrally and annulated in apical 1/3. Eyes reddish brown. Tips of the +anterior +mesonotal spines black. ii) +Brown form +( +Fig. 170 +): General colour greyish mid brown and often all over furnished with pale grey or whitish mottling and speckles; occasionally washed with some green. Tegmina and costal region of alae mid to purplish dark brown with the venations of a paler colour; anal region of alae dark red to purple with all veins marked by dark brown. Culture stock in Europe occasionally also produces intermediate forms, which are mostly green with the body to a variable degree furnished with well-defined bold chestnut-brown markings or with a brownish wash ( +Figs. 168 +, +391 +). + + +Head: Indistinctly longer than wide, strongly globose with cheeks parallel-sided. Vertex convex, covered with a variable number of differently sized tubercles and in centre armed with two ± prominent, pointed or blunt, conical horns; the dextral one carinate and the sinistral one considerably smaller ( +Figs. 173–174 +). Near posterior margin usually with a transverse row of four spiniform tubercles, the exterior ones sometimes enlarged. Often two further small granules are present on the cheeks. Eyes of moderate size, sub-circular and their length contained about +2x +in that of cheeks. Antennae slightly projecting over posterior margin of metanotum; consisting of about 45 antennomeres. Scapus dorsoventrally compressed, roundly rectangular and about 1.5x longer than wide. Pedicellus cylindrical, sub-spherical and less than half the length of scapus. Third antennomere slightly shorter than pedicellus. + + +Thorax: Pronotum slightly shorter and narrower than head, 1.3x longer than wide, gently constricted medially and with the +anterior +margin slightly widened. Transverse median depression distinct, slightly curved and almost reaching lateral margins of segment. Surface close to posterior margin with a pair of minute spiniform tubercles and in centre often with four small tubercles, which roughly form a square ( +Figs. 173–174 +). Mesothorax about 1.6x longer than head and pronotum combined, constricted anteriorly and gently widened towards the posterior. Mesonotum with a very faint longitudinal median carina and covered with a variable number of tubercles, which become more distinct towards the lateral margins and less numerous towards the posterior of segment; anteriorly with 1–3 pairs of ± prominent, forward directed spines ( +Figs. 173–174 +). Mesopleurae with a marginal row of 8–14 spiniform tubercles; metapleurae smooth or with a few small tubercles. Meso- and metasternum sparsely granulose. Tegmina oval, scale-like, with a very shallow central hump and very slightly projecting over posterior margin of metanotum. Alae slightly shorter than tegmina and reaching about half way along median segment. + + +Abdomen: Median segment longer than metanotum, 1.3x longer than wide and very gently widening towards the posterior; smooth. Segments II–VII almost parallel-sided and of uniform length, about 1.3x longer than wide; III and IV slightly broader than remaining. Tergites II and III occasionally with two small spine-like projections at posterior margin, II–VI otherwise smooth except for a few scattered granules. VI with two and VII with four fine longitudinal carinae. Lateral margins of VII slightly expanded posteriorly and forming a narrow, triangular lobe or tooth. Sternites II–VII smooth except for two very faint and short sub-parallel carinae close to posterior margin. Praeopercular organ formed by an elongate brown median hump close to posterior margin of sternum VII ( +Fig. 351 +). Tergites VIII–X roughly equal in width and considerably narrower than previous segments. VIII about 2/3 the length of VII and slightly constricted medially, IX quadrate and about 2/3 the length of VIII. Anal segment about as long as IX, with a slight longitudinal median carina, the posterior margin rounded and with a very small median indentation ( +Fig. 178 +). Epiproct slightly projecting over anal segment, shield shaped and roughly semi-circular with a keel dorsally ( +Fig. 178 +). Cerci very small, round in cross-section and conical with the apex pointed. Subgenital plate elongate and variable in length, lanceolate, longitudinally keeled and narrowed towards a rather acute apex; projecting over apex of abdomen by more than the length of anal segment ( +Figs. 177–178 +). + +Legs: All rather short and stocky. Profemora and mesofemora shorter than mesothorax, metafemora slightly projecting over posterior margin of abdominal segment III. Medioventral carina of profemora with 2–3 spines in apical portion, mesofemora with 4–6 and metafemora with 5–8 spines. Dorsal carinae of meso- and metafemora each with a ± prominent triangular lobe sub-apically (less distinct or sometimes lacking on metafemora), the posteroventral carina with one and the anteroventral carina with two pointed sub-apical spines. Anterodorsal carina of meso- and metatibiae occasionally with a ± distinct rounded to roundly triangular sub-basal and sub-apical expansion. Medioventral carina raised and rounded sub-basally and armed with a few small teeth in apical portion. Basitarsi about as long as following two tarsomeres combined. + + +FIGURES 171–176. + +Diapherodes jamaicensis +(Drury, 1773) + +. +171. +♂: captive reared from Jamaica [coll. FH, No. 0428-26]; +172. +♂: captive reared from Jamaica [coll. FH, No. 0428-35]; +173. +♀ head and pronotum: captive reared from Jamaica (specimen with large and irregularly tuberculose horns) [coll. FH, No. 0428-31]; +174. +♀ head and pronotum: captive reared from Jamaica (specimen with moderately sized, conical horns) [coll. FH, No. 0428-32]; +175. +♂ head and pronotum: Jamaica: Portland, Parrish (specimen two large +anterior +mesonotal spines) [FSCA]; +176. +♂ head and pronotum: captive reared from Jamaica (specimen with a cluster of six +anterior +mesonotal spines) [coll. FH, No. 0428-37]. + + + + +FIGURES 177–182. + +Diapherodes jamaicensis +(Drury, 1773) + +. +147. +♀ apex of abdomen (lateral view); +148. +♀ apex of abdomen (dorsal view); +149. +♂ apex of abdomen (lateral view); +150. +♂ apex of abdomen (dorsal view); +151. +Egg: captive reared from Jamaica (dorsal view) [coll. FH, No. 0428-E]; +152. +Egg: captive reared from Jamaica (lateral view) [coll. FH, No. 0428-E]. + + + + +♂ ( +Figs. 171–172 +, +388–389 +). + +Of moderate size (body length 63.0–94.0 mm) and rather slender for the + +jamaicensis + +species-group with well developed alae (32.0– +53.5 mm +); body surface sub-glabrous. General colouration bright green, the mesonotum with a slight yellowish wash. Tegmina green with a bold longitudinal white stripe along +anterior +margin. Costal region of alae slightly translucent green with a white longitudinal stripe running along the basal 1/3 of the +anterior +margin. Anal region translucent pink to orange ( +Fig. 171 +). Eyes reddish brown. Antennae reddish mid brown with the three or four basal antennomeres black ventrally. Pedicellus usually darker brown than all other antennomeres. +Anterior +spines of the mesonotum often black. Bases of all femora and tibiae ochre. Tarsi greenish brown. + + +Head: Similar in shape to ♀♀ but vertex much less convex and smooth except for two rounded unequal cephalad humps and two blunt tubercles close to the posterior margin; sometimes also with a few minute granules ( +Figs. 175–176 +). Eyes very prominent, sub-circular and projecting hemispherically; their length contained hardly more than once in length of cheeks. Antennae projecting over posterior margin of abdominal segment II and moderately robust; consisting of 57–60 antennomeres. Scapus oval in cross-section, roundly rectangular and about 1.3x longer than wide. Pedicellus cylindrical and about 2/3 the length of scapus. + + +Thorax: Pronotum somewhat shorter and narrower than the head, slightly trapezoidal and gradually narrowed towards the posterior; the posterior margin gently rounded. Median transverse depression distinct, gently curved and almost reaching lateral margin of segment. Surface smooth ( +Figs. 175–176 +). Mesothorax about +2x +longer than head and pronotum combined, mesonotum mostly with 1–4 pairs of prominent black, forward directed +anterior +spines ( +Figs. 175–176 +); rarely lacking. Posterior 2/3 of mesonotum and mesosternum sometimes with a few minute granules. Meso- and metapleurae as well as metasternum smooth. Tegmina elongate, oval, reaching 1/3 along median segment and with a blunt central protuberance, which is slightly displaced towards the +anterior +. Alae reaching to abdominal tergum VI. + + +Abdomen: Median segment gently narrowed towards the posterior. Segments II–VII parallel-sided and gradually decreasing in length; II 3.5x, VII 2.5x longer than wide. Sternites II–VII smooth. Tergum VIII ¾ the length of VII, widened towards the posterior and slightly tectate. IX ¾ the length of VIII, about as long as wide and very slightly narrowed towards the posterior. Anal segment about as long as IX with a slight longitudinal median carina, the posterior portion narrowed and rounded on both sides of the triangular median emargination ( +Fig. 180 +). Vomer with the base rather broad and roundly triangular, the terminal hook slightly up-curving and almost as long as basal portion ( +Fig. 371 +). Cerci almost as long as anal segment, slender, narrowed towards a blunt apex and very slightly in-curving ( +Fig. 371 +). Poculum convex, cymbiform, longitudinally carinate and with the posterior margin distinctly indented and bi-lobate medially ( +Fig. 179 +). + +Legs: Generally as in ♀♀ but relatively longer, more slender and lacking the dorsal armature of the meso- and metafemora and tibiae. Profemora roughly equal, mesofemora slightly shorter than mesothorax, metafemora reaching about half way along abdominal segment IV. Basitarsi a little longer than following two tarsomeres combined. + +Nymphs: +Newly hatched nymphs are bright yellowish green with brown antennae. Later instars and ♀ nymphs in particular tend to be various shades of brown rather than green like the adults. From 3rd instar on the lateral margins of tergum VII are conspicuously elevated and form a rounded lobe. The sub-apical dorsal teeth of the meso- and metafemora and dorsal elevations of the tibiae of ♀ nymphs are more prominent than in adults. ♂ nymphs may have small granules on the mesonotum. ♀ nymphs are very similar in general appearance to those of certain + +Haplopus + +-species. + + +Variability: +While ♂♂ merely show variability in the size and number of +anterior +spines of the mesonotum ( +Figs. 175–176 +), ♀♀ exhibit considerable variability in several aspects. Features generally showing variation are the number and size of the +anterior +spines of the mesonotum and armature of the head ( +Figs. 173–174 +), length of the subgenital plate and degree of the +anterior +armature of the mid and hind legs. Despite these morphological features ♀♀ occur in two distinct colour-forms described in detail above, which has caused the description of several synonyms. Specimens of the more common green form ( +Figs. 167, 169 +, +390 +) are averaging smaller than specimens of the more rarely encountered brown form ( +Fig. 170 +). Culture stock in Europe occasionally also produces green intermediate forms which are to a variable degree prettily furnished with rather geometrical chestnut-brown markings and possess a brownish hue all over the body ( +Fig. 168 +, +391 +). + + + +Egg ( +Figs. 181–182 +): + +The following description is based on a large number of eggs in the first author's collection (coll. FH) laid by captive reared specimens. + +Rather small, capsule 1.8x longer than wide and with dorsal surface more convex than ventral surface; polararea decidedly impressed if seen in lateral aspect. Capsule surface irregularly covered with raised ridge-like structures, tubercles and granules; a rather blunt longitudinal keel running from the micropylar plate to the polararea. Micropylar plate small, roughly heart-shaped and its length contained about 2.6x in that of capsule. Central portion of micropylar plate granulose, micropylar cup distinct and placed in posteromedian gap of plate. Operculum with a rim of irregularly raised tubercles; centre slightly lowered. General colour pale to mid brown, the outer margin of the micropylar plate and micropylar cup dark brown. +Measurements [mm]: Length 3.5–3.8, length (including operculum) 3.7–4.0, width 2.0–2.2, height 2.1–2.3, length of micropylar plate 1.3–1.4. + + + +Comments: +Drury's illustration of the ♂ HT does not show the +anterior +spines on the mesonotum mostly present and a very variable feature in + +D. jamaicensis + +. There are several old specimens in the collection NHMUK but none of these could be confirmed as Drury's +holotype +(personal communication with J. +Marshall +and P.D. Brock). Hence, the designation of a +neotype +may become necessary, but this deserves further evaluation and research in other collections, which are likely to contain specimens examined by Drury. + + + +Diapherodes glabricollis +Gray, 1835 + +was described from the ♀ and is the opposite sex of Drury's species ( +n. syn. +). Examination of the +holotype +of + +Diapherodes christopheri +Westwood, +1859 + +in OXUM leaves no doubt it is conspecific with + +D. jamaicensis +(Drury) + +( +n. syn. +). The type-locality “St. Christopher” [= +St. Kitts +] is however very doubtful and most certainly erroneous. Former authors distinguished + +D. christopheri + +from + +D. jamaicensis + +by the smooth metapleurae, which however is a variable feature in ♀♀ of + +jamaicensis + +. Both, + +D. pulverulentus +Gray, 1835 + +and + +H. murinus +Redtenbacher, 1908 + +are ♀♀ of the brown form of + +D. jamaicensis + +, hence also synonyms ( +n. syn. +). + + + + + +D. jamaicensis + +is being successfully reared in captivity in Europe from stock imported by Tony and Pat James ( +England +) in the late 1990's and has subsequently been included on the Phasmid Study Group culture-list as culture No. 214 “ + +Haplopus jamaicensis + +”. It readily accepts oak ( + +Quercus robur + +& + +Q. petraea + +, +Fagaceae +), eucalyptus ( + +Eucalytus gunnii + +, +Myrtaceae +), bramble ( + +Rubus fruticosus + +, +Rosaceae +), raspberry ( + +Rubus idaeus + +, +Rosaceae +), rose ( + +Rosa + +spp., +Rosaceae +), salal ( + +Gaultheria shallon + +, +Ericaceae +) and guava ( + +Psidium guajava + +, +Myrtaceae +) as alternative food plants and does well in moderately humid but well ventilated conditions. If adults are disturbed, both ♀♀ and ♂♂ will spread their pink hindwings. Males are very quick moving and capable of active flight. Mating usually takes place at night. + + + + +Distribution: +Jamaica +: Batia [ANSP]; Bath [USNM]; Liguanea Plain [MCZC; Moxey, 1972: 104, in litt.]; Quick Step nr. Aberdeen [USNM]; St. James, Montego Bay [NHMJ; Moxey, 1972: 104, in litt.]; Snug Harbour [ANSP]; Fountain Hill [NHMJ; Moxey, 1972: 104, in litt.]; Trelawny, Westwood [NHMJ; Moxey, 1972: 104, in litt.]; Manchester, Mandeville [NHMJ; Moxey, 1972: 104, in litt.]; Christiana [AMNH; Moxey, 1972: 104, in litt.]; St. Mary, Castleton Gardens [MCZC, Moxey, 1972: 104, in litt.]; St. Catherine, Boston Town Postal Agency [NHMJ; Moxey, 1972: 104, in litt.]; St. Andrew; Hermitage Reservoir [NHMJ; Moxey, 1972: 104, in litt.]; Blaudeville [NHMUK]; +Cinchona +[AMNH; Moxey, 1972: 104, in litt.]; Kingston [USNM]; Portland, Millbank [FSCA] & Portland Parish, Fellowship Rio Grande [USNM, NHMJ, Moxey, 1972: 104, in litt.]. Endemic. + + + + +Number of specimens examined: +134 + + + +TABLE 17. +Measurements of the green form of + +Diapherodes jamaicensis +(Drury, 1773) + + +n. comb. + +[mm] + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+♀, HT + +glabricollis + +[NHMUK] +♀ [NHMW]♀♀ ♂♂ captive reared captive reared [coll. FH] [coll. FH]♂ [NHMW]
Body (incl. sg. pl.)139.0137.5104.0–120.0 --
Body124.0126.0100.5–117.5 63.0–75.076.5
Pronotum5.65.24.6–4.8 2.5–2.83.2
Mesonotum23.823.017.8–20.5 9.8–11.913.8
Metanotum7.98.16.1–7.0 4.8–5.2-
Median segment8.08.36.2–7.1 6.6–7.0-
Tegmina10.99.67.1–8.1 7.0–9.17.4
Alae10.08.96.5–7.0 32.0–39.038.0
Profemora19.818.914.2–16.0 10.4–12.012.3
Mesofemora17.517.311.6–13.1 9.4–10.3-
Metafemora24.624.216.0–18.0 12.0–13.814.5
Protibiae19.218.212.8–14.8 10.0–11.911.5
Mesotibiae18.214.110.2–11.0 7.9–8.6-
Metatibiae24.020.214.5–25.5 10.3–12.112.3
Antennae-> 34.034.0–43.0 37.0–45.0> 29.5
+
+ + +TABLE 18. +Measurements of the brown form of + +Diapherodes jamaicensis +(Drury, 1773) + + +n. comb. + +[mm] + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+♀ HT + +pulverulentus + +[NHMUK] + +♀ LT + +murinus + +[NHMW] + +♀ PLT + +murinus + +[NHMW] +♀♀ [NHMUK]♂ [FSCA]
Body (incl. sg. pl.)120.5164.5132.5109.5–152.5-
Body109.0152.0121.0102.5–131.094.0
Pronotum4.85.45.14.7–5.73.9
Mesonotum20.127.022.817.9–26.315.3
Metanotum5.58.07.27.0–7.414.0**
Median segment7.29.48.16.2–9.9-
Tegmina7.811.28.07.3–10.311.2
Alae6.113.0> 9.06.8–9.053.5
Profemora16.520.516.315.1–18.315.7
Mesofemora13.417.214.413.2–16.314.9
Metafemora19.624.919.318.3–21.819.5
+
+ +......continued on the next page +** metanotum + median segment + +
+
+
\ No newline at end of file diff --git a/data/38/7F/30/387F3068D381FF27FF27EA4D26091AC4.xml b/data/38/7F/30/387F3068D381FF27FF27EA4D26091AC4.xml new file mode 100644 index 00000000000..b1654952c3d --- /dev/null +++ b/data/38/7F/30/387F3068D381FF27FF27EA4D26091AC4.xml @@ -0,0 +1,309 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + +Parhaplopus navarroi + +n. gen. +, n. sp. + + +(Figs. 310–321, 343, 356, 379) + + + +HT +, ♂: +Dominican Republic +, RD-095 Rodeo, ~ +0.5 km +E Presa de Blanco, Bonao, Monseñor Nouel Prov., +20.III.2003 +, D. Perez, R. Bastardo, B. Hierro. (night) [ +USNM +]. + + +PT +, ♀: +Dominican Republic +, Jardín Botánico Nacional, Santo +Domingo +, +20.IX.2000 +, +18°29.7’N +69°57.3’W +, D. E. Perez, R. H. Bastardo [ +USNM +]. + + +PT +, egg (removed from ovipositor): +Dominican Republic +, Jardín Botánico Nacional, Santo +Domingo +, +20.IX.2000 +, +18°29.7’N +69°57.3’W +, D. E. Perez, R. H. Bastardo [ +USNM +]. + + + + +Diagnosis: +Similar to the Cuban +P. c u be n s i s +(Saussure, 1868) but differing by: the smaller size and relatively shorter mesothorax of both sexes; more distinct pair of spines on the vertex ( +Figs. 304–306 +); less deflexed abdominal tergum VII ( +Fig. 308 +); narrowly rounded apex of the subgenital plate ( +Fig. 308 +) and less undulate dorsal carina of the protibiae of ♀♀, as well as the distinct white cheeks ( +Fig. 306 +) and more slender legs of ♂♂. + + + + +Etymology: +This pretty new species is dedicated to Santo Q. Navarro (Universidad Autónoma de Santo +Domingo +) for his invaluable support and assistance throughout the years to the collection efforts of the third author in +the Dominican +Republic. + + + + + +Description: ♀ ( +Fig. 310 +). + +Of medium size (body length including the subgenital plate +117.5 mm +) and fairly stocky for the genus. Colour greyish mid brown but the mesothorax and abdomen strongly darkened during preservation in the unique specimen at hand; abdominal sternites dull green posteriorly. Legs with a slight greenish wash and basal portion of profemora pale greyish green. Dorsal spines of the mesonotum with black tips, all other tubercles and spines of the head and thorax tipped with dull green. Antennae dark reddish brown ventrally and rather greyish mid brown dorsally. Eyes sepia with dull orange mottling. Tegmina and costal region of alae very dark brown and almost black laterally. Anal region of alae transparent grey with all major longitudinal and transverse veins broadly marked with dark grey or black. + + +Head: Ovoid, about 1.3x longer than wide ( +Fig. 312 +); vertex gently convex in the posterior portion and armed with a pair of moderately sized, conical cephalad spines as well as a number of smaller tubercles; two small granules are present on the cheeks ( +Fig. 313 +). Eyes rather small, circular and contained almost +3x +in length of cheeks. Antennae broken in the only specimen available. Scapus 2.3x longer than wide with the lateral margins gently rounded. Pedicellus less than half the length of scapus and longer than III, roughly cylindrical. + + + +FIGURES 310–314. + +Parhaplopus navarroi + +n. gen. +, n. sp.. +310. +♀ PT: Dominican Republic, Santo Domingo Province, Santo Domingo [USNM]; +311. +♂ HT: Dominican Republic, Monseñor Nouel Province, Bonao [USNM]; +312. +Head and pronotum of ♀ PT (dorsal view) [USNM]; +313. +Head and pronotum of ♀ PT (lateral view) [USNM]; +314. +Head and pronotum of ♂ HT (lateral view) [USNM]. + + + +Thorax: Pronotum slightly shorter and narrower than head, 1.4x longer than wide, roughly rectangular and with the lateral margins gently emarginated medially ( +Fig. 312 +). Transverse median sulcus distinct, gently curved and almost reaching lateral margins of segment. Dorsal surface with a slightly enlarged pair of spiniform tubercles just in front of posterior margin and otherwise with several irregularly disposed pointed tubercles ( +Fig. 312 +). Probasisternum with a median pair of tubercles, and two granules at each lateral margin. Profurcasternum with two small tubercles at lateral margins and two further tubercles at posterior margin. Mesothorax about +2x +longer than head and pronotum combined, rather broad and slightly down-curving in lateral aspect, constricted at the +anterior +and conspicuously swollen medially. Mesonotum gradually widened towards the mid of segment, then very gently rounded and in posterior portion almost parallel-sided. Surface all over armed with numerous prominent, irregularly paired, conical spines of variable sizes; in the median portion with a single conspicuously enlarged pair of spines. Along lateral margins a longitudinal row of about 10–14 pointed spines. Mesopleurae armed with a longitudinal row of about 12 small but acute spines, metapleurae with a marginal row of eight spiniform tubercles. Mesosternum with short, sparse tubercles, the metasternum with three pairs of small granules. Tegmina broadly ovate, coriaceous, with the venation very distinct, dense and irregularly disposed; roughly reaching to posterior margin of metanotum. The median protuberance rather shallow. Alae a little longer than tegmina and reaching about ¾ the way along median segment. + + +Abdomen: Median segment 1.8x longer than wide and roughly rectangular, surface smooth. Tergites II and III each with a few small tubercles, II–IV each with posteromedian pair of retrorse spines, which are most prominent on II; remaining segments unarmed. Segments II–VI roughly equal in length and about 1.8x longer than wide. Tergum VII shorter than previous and with the lateral margins gently rounded posteriorly ( +Fig. 316 +). VIII less than ¾ the length of VII and roughly 1.5x longer than wide. IX almost rectangular and about half the length of VIII. Anal segment almost parallel-sided but somewhat narrowed in posterior portion, with a small posteromedian emargination; epiproct very small and triangular ( +Fig. 316 +). Cerci very small and conical with a pointed apex; hardly projecting over posterior margin of anal segment ( +Fig. 315 +). Subgenital plate very long, naviculate, longitudinally carinate and with a gently expanded, rounded apex; extending over abdomen by more than the combined length of tergites VIII–X ( +Figs. 315–316 +). + +Legs: Pro- and mesofemora shorter than mesothorax and metafemora slightly projecting over posterior margin of abdominal segment III. Medioventral carina of profemora with three small spines, in mesofemora armed with four and on metafemora with five rather prominent spines. Anterodorsal carina of profemora and tibiae strongly raised and slightly undulate. Both outer ventral carinae of meso- and metafemora with two sub-apical spines, although smaller on the posterior carina; otherwise both carinae very minutely tuberculose. Both dorsal carinae slighty elevated sub-apically. Anterodorsal carina of mesotibiae gently rounded sub-basally and sub-apically. Probasitarsus about as long as the following three tarsomeres combined, dorsal carina rounded. Meso- and metabasitarsi simple and slightly shorter than following three tarsomeres combined. + + +♂ ( +Fig. 311 +). + +Of moderate size (body length 78.0mm) and fairly slender for the genus. Colour of body and front legs greenish mid brown, the metapleurae, metasternum and three terminal abdominal segments bright apple green. Mid and hind legs green with apices of the femora brown. Mesosternum whitish and the ventral surface of the abdomen dull green with white mottling. Cheeks mostly white ( +Fig. 314 +), eyes dark reddish brown. Spines of mesothorax with black tips. Tegmina and costal region of alae with +anterior +margin white, then a broad brown longitudinal band, and innermost portion bright apple green; in alae the brown longitudinal band with several washed greyish markings. Anal region of alae pale transparent pink with a slight greyish hue along the outer margin ( +Fig. 319 +) Antennae dark ochracheous and becoming darker towards the apex. + + +Head: Generally as in ♀♀ but only 1.2x longer than wide, with the vertex gently convex and smooth except for a pair of small but acute cephalad spines ( +Fig. 314 +). Eyes much more prominent, projecting hemispherically and their length contained only about 1.8x in that of cheeks. Antennae projecting over posterior margin of abdominal segment II; consisting of 59 segments. Otherwise as in ♀♀. + + +Thorax: Pronotum slightly shorter and narrower than head with the lateral margins very gently concave; surface smooth ( +Fig. 314 +). Transverse median sulcus shallow, gently rounded and almost reaching lateral margins of segment. Prosternum with a small median granule at each lateral margin. Mesothorax about +2x +longer than head and pronotum combined. Mesonotum armed with four pairs of moderately sized but pointed spines in the +anterior +2/3. Mesopleurae with a few small granules, metapleurae smooth. Mesosternum with three pairs of small tubercles, metasternum smooth. Tegmina oval and reaching almost half the way along median segment, central protuberance roundly conical. Alae reaching to posterior margin of abdominal segment VI (45.0 mm). + + +Abdomen: Segments II–IV roughly equal in length and almost +4x +longer than wide; all unarmed. V slightly shorter than previous and V–VII gradually decreasing in length with VII hardly +3x +longer than wide. +VIII 3 +/5 the length of VII and widened towards the posterior, IX about equal in length to VIII and constricted medially. Anal segment a little shorter than IX, widened towards the posterior and posterior margin with a deep triangular median emargination ( +Fig. 318 +). Epiproct very small and fully concealed by anal segment. Cerci slightly shorter than anal segment, laterally compressed and gradually narrowed towards a slender apex ( +Fig. 309 +). Vomer very broad, roundly triangular and with a very short, straight terminal hook ( +Fig. 356 +). Poculum moderately convex, scoopshaped and longitudinally carinate in posterior portion; reaching to posterior margin of tergum IX ( +Figs. 317–318 +). + + + +FIGURES 315–321. + +Parhaplopus navarroi + +n. gen. +, n. sp.. +315. +Apex of abdomen of ♀ PT (lateral view) [USNM]; +316. +Apex of abdomen of ♀ PT (dorsal view) [USNM]; +317. +Apex of abdomen of ♂ HT (lateral view) [USNM]; +318. +Apex of abdomen of ♂ HT (dorsal view) [USNM]; +319. +Right tegmen and ala of ♂ HT [USNM]; +320. +Egg PT (dorsal view) [USNM]; +321. +Egg PT (lateral view) [USNM]. + + +Legs: Pro- and mesofemora almost equal in length and slightly longer than mesothorax, metafemora reaching about half way along abdominal segment IV. All less carinate than in ♀♀ and lacking any dorsal elevations or teeth. Armature of medioventral carina of the femora as in ♀♀ but considerably less developed. Posteroventral carina of meso- and metafemora with only one small sub-apical spine. Tarsi relatively more elongate, probasitarsus almost equal in length to following three tarsomeres combined, meso- and metabasitarsus about as long as combined length of following two segments. Dorsal carina of probasitarsus very gently raised. + + +Egg ( +Figs. 320–321 +): + +A single fully developed egg was removed from the ovipositor of the +paratype +. Description as for the genus (see above). Measurements [mm]: Length 3.8, length (including operculum) 4.0, width 2.0, heigth 2.1, length of micropylar plate 1.2. + + + + +Comments: +The two +type +specimens are from separate localities but undoubtedly represent both sexes of the same species. The fact that only two specimens were encountered during as many as nine expeditions and collections at 280 sites throughout +the Dominican +Republic suggest this species to be rare. The conspicuous colouration of the unique known egg seems to be unusual and is perhaps an artifact or abnormality. + + + + + +Distribution ( +Fig. 379 +): + +Hispaniola ( +Dominican Republic +: Monseñor Nouel Prov. & Santo +Domingo +) [USNM]. + + + + +Number of specimens examined: +2 + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D385FF21FF27EA4C270B18B8.xml b/data/38/7F/30/387F3068D385FF21FF27EA4C270B18B8.xml new file mode 100644 index 00000000000..03ac97c6c67 --- /dev/null +++ b/data/38/7F/30/387F3068D385FF21FF27EA4C270B18B8.xml @@ -0,0 +1,220 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + +5.8. Genus + +Venupherodes + +n. gen. + + +Type-species: + +Platycrana venustula +Audinet-Serville, 1838: 242 + +, by present designation. + + + + + +Platycrana +, Audinet-Serville, 1838: 242 + +. + +Diapherodes +, Saussure, 1872: 185 + +. Redtenbacher, 1908: 434 (in part). Westwood, 1859: 84 (in part). + +Otte & Brock, 2005: 120 (in part). + + +Diapherodes + +(?), Kirby, 1904a: 362. + + + +Haplopus +, Redtenbacher, 1908: 429 + +(in part). + +Otte & Brock, 2005: 150 (in part). + + +Phasma +, Westwood, 1859: 34 + +, pl. 22: 7. + + + + + +Description: ♀♀, ♂♂ ( +Figs. 322–325 +). + +Small Haplopodini (body length < +80 mm +) with general appearance similar to + +Diapherodes +Gray, 1835 + +; ♂♂ indistinctly shorter than ♀♀. ♂♂ slender with scale-like tegmina and welldeveloped alae. ♀♀ apterous and rather broad insects with the body distinctly oval in cross-section and the thorax and abdomen conspicuously broadened. ♀♀ usually bright green but sometimes with washed blackish-brown portions, ♂♂ a mixture of mid green, dull green, creamish brown and white. Head of ♂♂ with a conspicuous white streak along the cheeks. Head globose, indistinctly longer than wide. Vertex roundly convex and indistinctly bicornute; sinistral tubercle often lacking. Antennae slender and as long as (♀♀), or considerably longer than head and thorax combined (♂♂). Scapus dorsoventrally flattened, longer than pedicellus. Pronotum with a ± prominent pair of blunt spines or spiniform tubercles +in anterior +half. Mesothorax of ♀♀ strongly broadened towards the posterior and constricted towards the +anterior +; roughly 1.5x the combined length of head and pronotum. Mesonotum conspicuously lyriform, being strongly broadened towards about 2/3 of its length and gently constricted in the posterior portion, laterally overlapping mesopleurae. Dorsal surface of mesonotum with a distinct, longitudinal median keel and +anterior +margin with a small pair of spiniform tubercles. Meso- and metapleurae granulose in ♀♀, unarmed in ♂♂. Mesosternum very minutely granulose in ♀♀ and smooth in ♂♂, metasternum smooth in both sexes. Abdomen of ♀♀ hardly longer than head and thorax combined and swollen medially; segment II–II increasing and V–X decreasing in width, IV widest segment. Segments II–VI wider than long. All tergites of ♀♀ finely multi-carinate, VII parallel-sided. Abdomen of ♂♂ slender and cylindrical with the terminal three segments just very slightly broader than previous. Praeopercular organ of ♀♀ formed by three small, wart-like tubercles which are arranged in a triangle close to posterior margin of sternum VII. Cerci very small (♀♀ in particular) and laterally compressed; almost straight. Epiproct very small and mostly hidden under anal segment. Subgenital plate of ♀♀ moderately, longitudinally keeled and tapered towards an acute apex; projecting over apex of abdomen by hardly more than the length of the anal segment. Vomer of ♂♂ very broad and roughly triangular, poculum moderately convex and with a blunt central spine. Legs of both sexes moderately slender and rather short in ♀♀, profemora about as long as (♂♂) or shorter than mesothorax (♀♀), hind legs not reaching apex of abdomen. All carinae of legs unarmed, except for spines on the medioventral carina and 1–2 small, sub-apical spines on the two outer ventral carinae of the meso- and metafemora. Basitarsi short, about as long as following two tarsomeres combined. + + + +Eggs ( +Figs. 332–333 +): + +Fairly small, capsule about 1.6x longer than wide and with dorsal surface more convex than ventral surface; polar area slightly impressed if seen in lateral aspect. Capsule surface irregularly but very prominently and unevenly sculptured being all over covered with raised ridge-like structures, tubercles and granules; a very blunt tuberculate longitudinal keel runs from the micropylar plate towards the polar-area. Micropylar plate impressed and lower than capsule surface, less than 1/3 the length of capsule, roughly oval, shield-shaped and 1.3x wider than long. Central portion of micropylar plate granulose, micropylar cup distinct and placed in a small posteromedian gap of plate. Operculum with an outer rim of irregularly raised tubercles; centre slightly lowered. General colour mid to dark brown, sometimes with a greyish wash, micropylar plate mid brown. + + + + +Differentiation: +The single Cuban representative of this new genus is easily distinguished from the closely related + +Diapherodes +Gray, 1835 + +(→ +Table 33 +). ♀♀ at once differ by being completely apterous, having a distinct longitudinal median keel on the mesonotum, a lyriform mesothorax which is distinctly widened laterally and overlaps the mesopleurae, and having a medially swollen and roundly expanded abdomen with IV being the widest segment. ♂♂ exhibit a very characteristic colouration, having the cheeks with a distinct white stripe and eggs are clearly distinguished by the broad and shield-shaped micropylar plate. + + + +The absence of wings in the ♀♀ resembles the second exclusively Cuban genus + +Aploploides +Rehn & Hebard, 1938 + +, which may be sympatric. This new genus however differs at first glance by: the globose and bi-cornute head, shorter cerci and armed thorax of both sexes, which is longitudinally keeled in ♀♀, as well as the more bulgy poculum of ♂♂. + + + + +Distribution ( +Fig. 374 +): + +Cuba +, endemic. + + + + +Etymology: +Neuter. The generic name is a combination of “ +Venu(s) +” (venus gr. = goddess of love), overtaken from the specific name “ + +venustula + +” of the type-species, and the ending “- +pherodes +” to indicate the close relation to + +Diapherodes +Gray, 1835 + +. + + + + + +Species included: + + + +1. + +Venupherodes venustula +(Audinet-Serville, 1838: 242) + +[ + +Platycrana + +]. +n. comb. += + +Phasma havaniense +Westwood, 1859: 34 + +, pl. 22: 7, 7a, 7b (♀). = + +Haplopus juvenis +Redtenbacher, 1908: 430 + +, pl. 20: 4 (♂). +n. syn. + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D387FF2FFF27EAE726151933.xml b/data/38/7F/30/387F3068D387FF2FFF27EAE726151933.xml new file mode 100644 index 00000000000..2d306f34c95 --- /dev/null +++ b/data/38/7F/30/387F3068D387FF2FFF27EAE726151933.xml @@ -0,0 +1,659 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Venupherodes venustula +(Audinet-Serville, 1838) + +n. gen. +, +n. comb +. + + + + +( +Figs. 322–333 +, +345 +, +364 +, +374 +, +384–387 +) + + + + + +Platycrana venustula +Audinet-Serville, 1838: 242 + +. +HT +, ♀: +Cuba +[MNHN—lost]. +NT +(by present designation), ♀: 800; + +Havaniense +(M. Leay) + +Westw., +Cuba +, Otto [MNHU]. + + + +Diapherodes venustula +, Westwood, 1859: 84 + +. + +Saussure, 1872: 185. +Bolivar, 1888: 140. +Redtenbacher, 1908: 435. +Rehn, 1909: 200. +Moxey, 1972: 117 (in litt.). +Otte & Brock, 2005: 121. +Rabaey & Simoens, 2007: 6, figs. [Culture report] + + +Diapherodes + +(?) + +venustula +, Kirby, 1904a: 362 + +. + + + +Phasma (Diapherodes) venustulum +, de Haan, 1842: 109 + +. + + + +Phasma havaniense +Westwood, 1859: 34 + +, pl. 22: 7 (♀). +HT +, ♀: Ins. Havannah; Type—Westwood, + +Phasma havaniense, +Cat. Phasm. 1859 + +, p. 24, pl. +22 f. +7; + +Pleseophyllum +Havaniense + +; +Type +Orth: 615, + +Phasma havaniense +Westw., Hope Dept. Oxford + +[OXUM, No. 615]. [Synonymised by Saussure +1871–1872 +: 185] Moxey, 1972: 117 (in litt.). Otte & Brock, 2005: 121. + + + +Haplopus juvenis +Redtenbacher, 1908: 430 + +, pl. 20: 4 (♂). +LT +(by present designation), ♂: Coll. Br. v. W., ex. Coll. Sommer, +Cuba +; det. Br. v. W., + +Haplopus juvenis + +(specimen with open wings) [NHMW, No. 795]; +PLT +, ♂: Coll. Br. v. W., ex. Coll. Sommer, +Cuba +; det. Br. v. W., + +Haplopus juvenis + +[NHMW, No. 795]; +PLT +, ♂: Coll. Br. v. W., ex. Coll. Sommer, +Cuba +; det. Br. v. W., + +Haplopus juvenis + +, 77.; 7647, + +jamaicensis + +, +Cuba +[NHMW, No. 795]; +PLT +, ♂: Coll. Br. v. W., ex. Coll. Sommer, +Cuba +; det. Br. v. W., + +Haplopus juvenis + +; 7647; 7647 + +Phasma jamaicensis +Fabr. Drur. + +, + +Spectrum viride +Stoll + +, capta T. Müller, +Cuba +, Phas. Inv. Nr. 795 [NHMW, No. 795]. +n. syn. + +Rehn, 1909: 200. + +Moxey, 1972: 117 (in litt.). [Listed as a synonym of + +Diapherodes venustula +(Audinet-Serville, 1838) + +—unpublished] Otte & Brock, 2005: 151. + + + +Aplopus juvenis +, Brock, 1998a: 57 + +. + + + + +Further material [78 ♂♂, 53 ♀♀, 3 nymphs, eggs]: +CUBA +: + + +1 ♀: Coll. Br. v. W., +Kuba +, Saussure; det. Br. v. W. + +Diapherodes venustula + +; 11.165; 11.165 + +Diapherodes venustula +Serv. ( +Havaniensis +) + +♀ [ +NHMW +, No. 840]; 1 ♀: + +Diapherodes venustula +, Serv. + +; +Cuba +(Lembeye) [ +MNCN +]; 1 ♀: + +Diapherodes venustula + +, +Cuba +, Gundlach [ +MNCN +]; +1 ♂ +(penultimate instar): +Cuba +, Cabrara [ +MNCN +]; 1 ♀, 2 ♂♂: +Cuba +, achété par M. Poey; + +Diapherodes venustula +Serv. + +( +MHNG +); 2 ♀♀, 2 ♂♂: +Cuba +, Mr. H. de Saussure; + +Diapherodes venustula +Serv. + +[ +MHNG +]; +1 ♂ +: +Cuba +, coll. Guerin; + +Diapherodes venustula +Serv. + +[ +MHNG +]; +1 ♂ +, 1 ♀ (nymph): +Cuba +; + +Diapherodes venustula +Serv. + +[ +MHNG +]; 2 ♂♂: 836; + +venustula +(Westw.) + +, +Platycr. + +venustula +Serv. + +, +Cuba +, Otto [ +MNHU +]; 1 ♀, +1 ♂ +: ex Zucht: K. Rabaey ( +Belgien +), Herkunft: W-Cuba, leg. I. Fritzsche, +VII.2006 +[coll. FH, No’s 0599- 1 & 3]; +1 ♂ +: ex Zucht: F. Hennemann, urspr.: +CUBA +, leg. I. Fritzsche, +VII.2006 +[coll. FH, No. 0599-2]; 13 ♀♀, 18 ♂♂, +1 ♂ +(penultimate instar), eggs: ex Zucht: F. Hennemann 2007/2008, Herkunft: W-Cuba, Pinar del Rio Provinz, leg. I. Fritzsche 2005 [coll. FH, No’s 0599-4 to 35 & E]; 1 ♀, 2 ♂♂: ex Zucht F. Hennemann 2008/09, Herkunft: W-Cuba, Pinar del Rio Provinz, leg. I. Fritzsche 2005 [coll. FH, No’s 0599-36 to 38]; +1 ♂ +: Sierra Rangel, de Rio—1934; Roberts Coll.; wO172 [ +ANSP +]; +1 ♂ +, 1 ♀: Somorrostro, Havana, +Aug. 20, 35 +, Schramuzza, y. Brunner [ +ANSP +]; +1 ♂ +, 1 ♀: Marianao, +Cuba +, Aug. (From. T. Barbouy) [ +ANSP +]; 30 ♀♀, 46 ♂♂, eggs: ex Zucht O. Conle, Herkunft: W-Cuba, Pinar del Rio Provinz [coll. OC]. + + + + + +Description: ♀ ( +Figs. 322–324 +, +384 +, +386–387 +). + +Small (body length including subgenital plate 65.0–80.0 mm) and robust Haplopodini (maximum body width at abdominal segment IV 8.0–10.0 mm) with a strongly broadened mesothorax and medially swollen abdomen. Colour of body and head bright apple green with the ventral body surface dull green. Sometimes specimens occur which have certain parts of the dorsal body surface furnished with irregular washed brownish or blackish markings ( +Figs. 324 +, +387 +); more rarely blackish markings are seen on the ventral surface of the abdomen. Rather frequently specimens have the head dull brownish green or almost entirely brown. +Anterior +margin of pronotum yellow. +Anterior +portion of the lateral margins of mesonotum ochre, meso- and metapleurae ochre with a broad, white longitudinal stripe along ventral margin. Coxae reddish brown. Cerci pale to dark brown. Front legs greenish brown with the basal portion of the femora pale green. Mid and hind legs pale to mid green with the base of the femora slightly brownish. Basitarsi green, remaining tarsomeres brown. Scapus and pedicellus mid to dark brown. Remainder of antennae pale brown and each antennomere with a fine transverse dark band at the apex; this turning to black towards apex of antennae. Eyes reddish brown with pale cream markings. + + +Head: Globose, indistinctly longer than wide, and considerably broader than prothorax. Vertex convex, with a few small, scattered granules and in centre mostly armed with a blunt, conical dextral tubercle; the sinistral one faint or obsolete ( +Fig. 326 +). Eyes convex, almost circular and of moderate size; their length contained about 1.8x in that of cheeks. Antennae slender and hardly reaching posterior margin of median segment; with about 45 antennomeres. Scapus dorsoventrally compressed, about +2x +longer than wide and constricted at the base. Pedicellus cylindrical and about half as long as scapus. + + +Thorax: Pronotum about as long but distinctly narrower than head and strongly tapered towards the posterior; +anterior +margin about 1.3x wider than posterior margin and median portion very gently constricted. Transverse median sulcus very distinct, slightly curved but just not reaching lateral margins of segment. +Anterior +half with a pair of prominent, blunt spines and close to posterior margin with two small tubercles; otherwise smooth ( +Fig. 326 +). Mesothorax about 1.5x longer than head and pronotum combined and strongly constricted anteriorly; posterior margin about +3x +wider than +anterior +margin. Mesonotum roughly +2x +longer than wide and distinctly lyriform, being strongly broadened towards about 2/3 of its length and gently constricted in the posterior portion. Lateral margins strongly rounded in medial portion and overlapping the mesopleurae. Entire dorsal surface of mesonotum with a distinct longitudinal median keel, close to the +anterior +margin with a small pair of ± distinct tubercles ( +Fig. 326 +) and with a few rounded granules along the lateral margins; otherwise smooth. Lateral margins very minutely denticulate. Mesopleurae with a fine longitudinal keel close to +anterior +margin and with a median row of granules. Metapleurae slightly tectiform with an acute longitudinal median keel, unarmed. Mesosternum smooth or with a very few scattered granules, metasternum smooth. Metanotum less than 1/3 the length of mesonotum and roughly quadrate; dorsal surface with a faint longitudinal median keel. + + + +FIGURES 322–325. + +Venupherodes +venustula +(Audinet-Serville, 1839) + +n. gen. +, n. comb.. +322. +♀: captive reared from NW- Cuba, Pinar del Rio [coll. FH, No. 0599-13]; +323. +♀: captive reared from NW-Cuba, Pinar del Rio [coll. FH, No. 0599-3]; +324. +♀: captive reared from NW-Cuba, Pinar del Rio [coll. FH, No. 0599-20]; +325. +♂: captive reared from NW-Cuba, Pinar del Rio [coll. FH, No. 0599-1]. + + + + +FIGURES 326–333. + +Venupherodes +venustula +(Audinet-Serville, 1839) + +n. gen. +, n. comb.. +326. +Head and pronotum of ♀: captive reared from NW-Cuba, Pinar del Rio [coll. FH, No. 0599-6]; +327. +Head and pronotum of ♂: captive reared from NW- Cuba, Pinar del Rio [coll. FH, No. 0599-2]; +328. +Apex of ♀ abdomen: captive reared from NW-Cuba, Pinar del Rio (lateral view); +329. +Apex of ♀ abdomen: captive reared from NW-Cuba, Pinar del Rio (dorsal view); +330. +Apex of ♂ abdomen: captive reared from NW-Cuba, Pinar del Rio (lateral view); +331. +Apex of ♂ abdomen: captive reared from NW-Cuba, Pinar del Rio (dorsal view); +332. +Egg: captive reared from NW-Cuba, Pinar del Rio (dorsal view) [coll. FH, No. 0599-E]; +333. +Egg: captive reared from NW-Cuba, Pinar del Rio (lateral view) [coll. FH, No. 0599-E]. + + + +Abdomen: Median segment slightly longer than metanotum, a little longer than wide and very gently widening towards the posterior. Dorsal surface with a faint longitudinal median keel, otherwise smooth. Abdomen swollen medially with II–III widening, V–X narrowing and IV broadest segment ( +Fig. 322 +). Tergites II–IV transverse with IV almost +2x +wider than long, VII slightly longer than wide. Tergites II–IX each with four distinct, longitudinal and roughly parallel carinae; two close to the median line and one on each side about half way towards the lateral margin. The two median carinae are melted together to form a single blunt carina on VIII–X. Sternites II–VII smooth. Praeopercular organ formed by three small, wart-like granules close to posterior margin of sternum VII; these roughly arranged as a triangle ( +Fig. 345 +). Tergum VIII about ¾ the length of VII and strongly convex. IX slightly wider than long and about 2/3 the length of VIII. Anal segment about as long as IX, flattened and gradually tapered towards the posterior; posterior margin rounded and with a small median notch and lateral margins somewhat emarginated medially ( +Figs. 328–329 +). Epiproct very small, slightly projecting over anal segment, semicircular and with a keel dorsally. Cerci mostly hidden underneath anal segment; finely bristled. Subgenital plate longitudinally keeled and tapered towards an acute apex; projecting over apex of abdomen by about 1.5x the length of the anal segment ( +Figs. 328–329 +). + +Legs: All fairly short, profemora and mesofemora shorter than mesothorax and metafemora slightly projecting over posterior margin of abdominal segment IV. Two outer ventral carinae of meso- and metafemora each with 1–2 small but pointed sub-apical spines. Medioventral carina of profemora with 1–2 small sub-apical spines, of meso- and metafemora with five moderately strong spines, which increase in size towards the apex of femur. Dorsal carina of the probasitarsus very gently rounded, all basitarsi roughly as long as following two tarsomeres combined. + + +♂ ( +Figs. 325 +, +385–386 +). + +Fairly small (body length 54.5–68.0 mm) and moderately slender insects with well developed alae (29.5–35.0 mm) and a very characteristic colouration. General colour of head and dorsal body surface mid to dull green. Ventral body surface creamish mid brown, sometimes with a slight greenish wash. Head with a bold white longitudinal stripe along the cheeks ( +Fig. 327 +). Pronotum ochre with the central portion green. Mesonotum mid to dull green with the +anterior +and lateral margins broadly ochre to mid brown. Greatest parts of metapleurae bright apple green. Tegmina and costal region of alae mid to dull green with the +anterior +margin brown and towards the interior bordered by a longitudinal whitish stripe. Central hump of tegmina sometimes dull yellow. Anal region translucent orange. Eyes reddish brown with pale cream markings. Antennae generally as in ♀♀. Fore legs brownish green, mid and hind legs mid to dull green with the bases of the femora pale green. Tarsi greenish brown with the basitarsus green. In addition to the typical colour-form here described, considerably darker specimens frequently occur amongst captive reared specimens. These have the mid and hind legs, tegmina and costal region of the alae very dark green and the mesothorax almost entirely brown, even the metapleurae are dull instead of apple green. It is not known whether such varieties also occur in the wild. + + +Head: Generally as in ♀♀ but vertex slightly less convex and the two cephalad tubercles more distinct ( +Fig. 327 +). A small C-shaped impression between the bases of the antennae. Eyes of moderate size, circular and strongly convex; their length contained less than 1.5x in that of cheeks. Antennae moderately thickened and ± reaching to posterior margin of abdominal segment III. Otherwise as in ♀♀. + + +Thorax: Pronotum slightly shorter and narrower than the head, slightly trapezoidal and gradually narrowed towards the posterior; posterior margin rounded. Median transverse depression very distinct, gently curved and almost reaching lateral margin of segment; armature as in ♀♀ but posterior pair of tubercles indistinct to obsolete ( +Fig. 327 +). Mesothorax elongate, roughly +2x +longer than head and pronotum combined, cylindrical and slightly widened at the posterior. +Anterior +margin of mesonotum usually with one or two pairs of blunt spine-like tubercles or spines ( +Fig. 327 +); sometimes lacking. Surface otherwise with a few irregular, minute granules. Mesopleurae with a few small granules arranged in a longitudinal row, metapleurae as well as meso- and metasternum smooth. Tegmina oval, reaching about 1/3 the way along median segment and with a shallow central hump. Alae reaching to abdominal tergum VI. + + +Abdomen: Median segment considerably longer than metanotum, gently narrowed towards the posterior; smooth. Segments II–VII, elongate, cylindrical, parallel-sided and gradually decreasing in length; II almost +4x +and VII just 2.6x longer than wide. Tergites II–VI and sternites II–VII smooth; tergites VI–X with a fine longitudinal median carina. VIII–X indistinctly broader than previous. VIII ¾ the length of VII and very slightly widened towards the posterior. IX a little shorter than VIII, slightly longer than wide and very gently constricted medially. Anal segment 3/5 the length of IX slightly widened towards the posterior and the posterior margin rounded with a broad triangular median indentation ( +Fig. 331 +). Epiproct very small and hidden underneath anal segment. Vo m e r large, flattened and broadly triangular with a very short terminal hook ( +Fig. 364 +). Cerci about 2/3 the length of anal segment, slender, strongly laterally compressed and very gently in-curving. Poculum moderately convex, cup-like, acutely carinate longitudinally and with the posterior margin notched medially; reaching about ¾ along tergum IX ( +Figs. 330 +, +364 +). + +Legs: Generally as in ♀♀ but relatively longer and more slender. Profemora about equal in length to mesothorax, mesofemora shorter than mesothorax, metafemora reaching about 2/3 the way along abdominal segment IV. + +Nymphs: +Newly hatched nymphs are slender and have a body length of ± 16.0 mm. The body, fore legs and antennae are greenish brown, the head, mid and hind legs bright green and the tarsi brown. Later instars vary from dull green over various shades of brown, often irregularly furnished with pale or dark mottling. The legs are pale green to straw. It is interesting to note that nymphs generally resemble those of various + +Diapherodes + +and + +Haplopus + +- species, exhibiting rounded lateral lobes on abdominal tergum VII which disappear in the adult stage. Furthermore, the typical body shape of ♀♀ does not occur before the final ecdysis, even penultimate instar nymphs having a rather slender body. + + +Variability: +In adults insects considerable variability is limited to the size and colouration. Slight variability is also seen in the length/width-relation of the mesothorax of ♀♀ as well as the size of the spines on the vertex, pronotum and +anterior +portion of the mesonotum (the latter ones may be missing). In addition to the usual plain green specimens ones may occur that are washed with dark brown, or have certain body-parts brownish ( +Fig. 316 +). + + + +Egg ( +Figs. 332–333 +): + +Description as for the genus (see above). Measurements [mm]: Length 3.1–3.5, length (including operculum) 3.7–3.9, width 1.9–2.2, height 2.2–2.6, length of micropylar plate 1.1–1.2. + + + + +Comments: +Audinet-Serville (1838: 242) described + +Platycrana venustula + +based on a single ♀ which he stated to be deposited in the “Collection de la Société entomologique de +France +”. This is now held in MNHN but extensive search has not revealed a single specimen of this species in the entire collection. Therefore, the +holotype +must be regarded lost (Otte & Brock, 2005: 121) and a ♀ in MNHU is here selected as the +neotype +to guarantee stability of Audinet-Serville's taxon. + +Phasma havaniense +Westwood, 1859 + +was described based on a ♀ from Havana in OXUM and was correctly synonymised with + +P. venustula + +by Saussure (1872: 185). The corresponding ♂♂ were described by Redtenbacher (1908: 429) as + +Haplopus juvenis + +which consequently becomes a synonym of + +V. venustula + +( +n. syn. +). + + +Culture-stock of + +V. venustula + +originating in the Pinar del Rio Province was imported to +Germany +by I. Fritzsche (Wernigerode, +Germany +) in 2005. This has proven fairly easy to rear in captivity and was included on the Phasmid Study Group culture-list as culture No. 283. A warm, rather dry and well ventilated climate is preferred in captivity. +Eucalyptus +( + +Eucalyptus + +spp., +Myrtaceae +), oaks ( + +Quercus robur + +, + +Q. rubra + +and + +Q. ilex + +, +Fagaceae +), salal ( + +Gaultheria shallon + +, +Ericaceae +) and St. John's Wort ( + +Hypericum patulum + +, +Hypericaceae +) are accepted as alternative food plants. Eggs have a rather short incubation period of only 10–12 weeks at an average temperature of 25°C. About 3– +4 +eggs are laid per day and ♀, each of which produces a total of 150– +200 +eggs. Mating takes place exclusively at night and lasts for one to three hours. + + + + + +Distribution ( +Fig. 374 +): + +NW-Cuba (Havanna [OXUM]; Mariano [ANSP]; Somorrostro [ANSP]; Cabrera [MNCN];Sierra Rangel, Pinar del Rio [ANSP]; Pinar del Rio [coll. FH, coll. OC]). + + + + +Number of specimens examined: +140 + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D394FF31FF27E82920461BB1.xml b/data/38/7F/30/387F3068D394FF31FF27E82920461BB1.xml new file mode 100644 index 00000000000..7a5b52bab85 --- /dev/null +++ b/data/38/7F/30/387F3068D394FF31FF27E82920461BB1.xml @@ -0,0 +1,83 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Aploploides +Rehn & Hebard, 1938 + + + + + +Type-species: + +Aploploides stenocephalum +Rehn & Hebard, 1938: 49 + +, by original designation of Rehn & Hebard, 1938: 49) + + + + +1. + +Aploploides stenocephalum +Rehn & Hebard, 1938: 49 + +, pl. 4: 18–21 (♂, ♀). + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D394FF31FF27E97B20241AC2.xml b/data/38/7F/30/387F3068D394FF31FF27E97B20241AC2.xml new file mode 100644 index 00000000000..d4c30f97a50 --- /dev/null +++ b/data/38/7F/30/387F3068D394FF31FF27E97B20241AC2.xml @@ -0,0 +1,85 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Apteroplopus + +n. gen. + + + + + +Type-species: + +Dyme +grosse-tuberculata + +Brunner v. Wattenwyl, 1907: 323, by present designation + +1. + +Apteroplopus +grosse-tuberculatus + +(Brunner v. Wattenwyl, 1907: 323) [ + +Dyme + +]. + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D396FF33FF27EEC026491C0F.xml b/data/38/7F/30/387F3068D396FF33FF27EEC026491C0F.xml new file mode 100644 index 00000000000..231909b5988 --- /dev/null +++ b/data/38/7F/30/387F3068D396FF33FF27EEC026491C0F.xml @@ -0,0 +1,103 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Parhaplopus + +n. gen. + + + + + +Type-species: + +Haplopus cubensis +Saussure, 1868: 68 + +, by present designation) + +1. + +Parhaplopus cubensis +(Saussure, 1868: 68) + +[ + +Haplopus + +]. +n. comb. +2. + +Parhaplopus evadne + +(Westwood, 1859: 85, pl. 18: 6, 6a & b (♂)) [ + +Haplopus + +]. +n. comb. +3. + +Parhaplopus navarroi + + +n. sp. + + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D396FF33FF27EF38206B1F57.xml b/data/38/7F/30/387F3068D396FF33FF27EF38206B1F57.xml new file mode 100644 index 00000000000..2ce37c0649f --- /dev/null +++ b/data/38/7F/30/387F3068D396FF33FF27EF38206B1F57.xml @@ -0,0 +1,100 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Venupherodes + +n. gen. + + + + + +Type-species: + +Platycrana venustula +Audinet-Serville, 1838: 242 + +, by present designation + +1. + +Venupherodes venustula +(Audinet-Serville, 1838: 242) + +[ + +Platycrana + +]. +n. comb. + + + += + +Phasma havaniense +Westwood, 1859: 34 + +, pl. 22: 7, 7a, 7b (♀). = + +Haplopus juvenis +Redtenbacher, 1908: 430 + +, pl. 20: 4 (♂). +n. syn. + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D397FF32FF27E96420AF1AFC.xml b/data/38/7F/30/387F3068D397FF32FF27E96420AF1AFC.xml new file mode 100644 index 00000000000..22575ee1c1b --- /dev/null +++ b/data/38/7F/30/387F3068D397FF32FF27E96420AF1AFC.xml @@ -0,0 +1,93 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Paracranidium +Brock, 1998 + + + + + +Type-species: + +Diapherodes +( +Cranidium +) +pumilio +Westwoood, 1843: 50 + +, pl. 61: 2, by original designation of Brock, 1998: 28. + + + + +1. + +Paracranidium pumilio + +(Westwood, 1843: 50, pl. 61: 2 (♀)) [ + +Diapherodes +( +Cranidium +) + +]. + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D397FF32FF27EA3426621A4A.xml b/data/38/7F/30/387F3068D397FF32FF27EA3426621A4A.xml new file mode 100644 index 00000000000..f4ef9b7dddb --- /dev/null +++ b/data/38/7F/30/387F3068D397FF32FF27EA3426621A4A.xml @@ -0,0 +1,216 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Haplopus +Burmeister, 1838 + + + + + +Type-species: + +Cyphocrana micropterus +St. Fargeau & Audinet-Serville, 1825: 445 + +, by monotypy. + + + + += + +Aplopus +Gray, 1835: 13 + +, 34. + + + + +1. + +Haplopus bicuspidatus +de Haan, 1842: 128 + +. + + +2. + +Haplopus brachypterus + + +n. sp. + + + +3. + +Haplopus intermedius + + +n. sp. + + + +4. + +Haplopus micropterus +(St. Fargeau & Audinet-Serville, 1828: 445) + +[ + +Cyphocrana + +]. = + +Phasma angulata +Stoll, 1813: 61 + +, pl. 21: 77 (♀). = + +Haplopus bituberculatum +de Haan, 1842: 128 + +. +n. syn. += + +Haplopus cythereus +Westwood, 1859: 86 + +, pl. 18: 5, 5a & b (♂). +n. syn. += + +Haplopus ligia +Westwood, 1859: 89 + +, pl. 1: 1, 1a, 1b (♂) & 2, 2a (♀). +n. syn. += + +Haplopus ligiolus +Redtenbacher, 1908: 430 + +. +n. syn. += + +Haplopus obtusus +Redtenbacher, 1908: 431 + +. +n. syn. += + +Diapherodes spinipes +Gray, 1835: 34 + +. +n. syn. + + +5. + +Haplopus scabricollis +(Gray, 1835: 34) + +[ + +Diapherodes + +]. = + +Aplopus mayeri +Caudell, 1905: 83 + +. +n. syn. + + + + += + +Aplopus similis +(Rehn, 1904: 65) + +. +n. syn. + + +6. + +Haplopus sobrinus + + +n. sp. + + + +7. + +Haplopus woodruffi + + +n. sp. + + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D397FF32FF27EEC026241C2A.xml b/data/38/7F/30/387F3068D397FF32FF27EEC026241C2A.xml new file mode 100644 index 00000000000..42e9b29242b --- /dev/null +++ b/data/38/7F/30/387F3068D397FF32FF27EEC026241C2A.xml @@ -0,0 +1,111 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Cephaloplopus + +n. gen. + + + + + +Type-species: + +Cephaloplopus pulchellus + + +n. sp. + +, by present designation + +1. + +Cephaloplopus alope + + +n. sp. + + + + +2. + +Cephaloplopus euchlorus + + +n. sp. + + + +3. + +Cephaloplopus laetus + + +n. sp. + + + +4. + +Cephaloplopus pulchellus + + +n. sp. + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D397FF32FF27EFC4271B197A.xml b/data/38/7F/30/387F3068D397FF32FF27EFC4271B197A.xml new file mode 100644 index 00000000000..a7db8aeb302 --- /dev/null +++ b/data/38/7F/30/387F3068D397FF32FF27EFC4271B197A.xml @@ -0,0 +1,226 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Diapherodes +Gray, 1835 + + + + + +Type-species: + +Mantis gigantea +Gmélin, 1789: 2055 + +, by subsequent designation of Kirby, 1904a: 362. + + + + +1. + +Diapherodes achalus +(Rehn, 1904: 68) + +[ + +Aplopus + +]. +n. comb. += + +Diapherodes longiscapha +Redtenbacher, 1908: 435 + +. +n. syn. + + +2. + +Diapherodes angulata +(Fabricius, 1793: 13) + +[ + +Mantis + +]. +rev. stat. += + +Haplopus grayi +Kaup, 1871: 36 + +. +n. syn. + + +3. + +Diapherodes dominicae +(Rehn & Hebard, 1938: 53) + +. +n. comb. + + +4. + +Diapherodes gigantea gigantea +(Gmélin, 1789: 2055) + +[ + +Mantis + +]. = + +Mantis gigas +Drury, 1773: 89 + +, pl. 50 (♀). + + + + += + +Cyphocrana cornuta +St. Fargeau & Audinet-Serville, 1825: 445 + +. + + +5. + +Diapherodes gigantea saintluciae + + +n. ssp. + + + +6. + +Diapherodes jamaicensis + +(Drury, 1773: 88, pl. 44: 1 (♂)) [ + +Mantis + +]. +n. comb. += + +Mantis bispinosa +Fabricius, 1775: 274 + +. + + += + +Haplopus christopheri +Westwood, 1859: 84 + +, pl. 33: 4, 4a (♀). +n. syn. += + +Diapherodes glabricollis +Gray, 1835: 33 + +. +n. syn. + + += + +Haplopus murinus +Redtenbacher, 1908: 429 + +. +n. syn. += + +Dipaherodes pulverulentus +Gray, 1835: 34 + +. +n. syn. + + +7. + +Diapherodes laevicollis +Redtenbacher, 1908: 434 + +. + + +8. + +Diapherodes martinicensis +Lelong & Langlois, 2005: 264 + +. + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D3A7FF09FF27EDBE21E51AAD.xml b/data/38/7F/30/387F3068D3A7FF09FF27EDBE21E51AAD.xml new file mode 100644 index 00000000000..651bea1bd81 --- /dev/null +++ b/data/38/7F/30/387F3068D3A7FF09FF27EDBE21E51AAD.xml @@ -0,0 +1,1175 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + +Haplopus scabricollis +(Gray, 1835) + + +(Figs. 257–275, 341, 361–362) + + + +Diapherodes scabricollis +Gray, 1835: 34 + +. +LT +(by present designation), ♂: no data [possibly from +the Bahamas +→ see comments below] [ +LSUK +]; +PLT +, ♀: no data [ +LSUK +]. + +Moxey, 1972: 110 (in litt.). + + + + +Haplopus scabricollis +Westwood, 1859: 88 + +. + +Kirby, 1904a: 364. + + +Redtenbacher, 1908: 432. +Otte & Brock, 2005: 152. + + + + +Aplopus mayeri +Caudell, 1905: 83 + +. +HT +, ♂: Loggerhead Key, Dry +Tortugas +, Fla; +Catal +. No. 54; + +Aplopus mayeri +Caud. + +♂ +TYPE +; +Type +No. 42774 +U.S. +N.M. [USNM]; +AT +, ♀: Loggerhead Key, Dry +Tortugas +, Fla; +Catal +No. 54; + +Aplopus mayeri +Caud. + +♀ +Type +; Brooklyn Museum Coll. 1929; Allotype No. 42774 +U.S. +N.M. [USNM]; +PT, +♂: Loggerhead Key, Dry +Tortugas +, Fla; +Catal +. No. 54; Brooklyn Museum Coll. 1929; +Paratype +No. 42774 +U.S. +N.M. [USNM]; +PT, +♀: Loggerhead Key, Dry +Tortugas +, Fla; +Catal +. No. 54; Brooklyn Museum Coll. 1929; +Paratype +No. 42774 +U.S. +N.M. [USNM]; +PT, +♀: Loggerhead Key, Florida, Dry +Tortugas +; +Paratype +No. 42774 +U.S. +N.M.; + +Aplopus mayeri +Caudell + +♀ +Paratype +[USNM]; +PT, +♀ (penultimate instar): Loggerhead Key, Dry +Tortugas +, Fla; +Catal +. No.54; Brooklyn Museum Coll. 1929; +Paratype +No. 42774 +U.S. +N.M. [USNM]; +PT, +♀ (nymph n4): Florida. Loggerhead Key; +Catal +. No. 54; Brooklyn Museum Coll. 1929; +Paratype +No. 42774 +U.S. +N.M. [USNM]; +PT, +♂ (nymph n4): Loggerhead Key, Dry +Tortugas +, Fla; +Catal +. No. 54; +Paratype +No. 42774 +U.S. +N.M. [USNM]; +PT, +♀ (nymph n5): Loggerhead Key, Dry +Tortugas +, Fla; +Catal +. No. 54; Brooklyn Museum Coll. 1929; +Paratype +No. 42774 +U.S. +N.M. [USNM]; +PT, ♂ +(in Ryker mount): Loggerhead Key Florida, Dry +Tortugas +, Dr. Mayer; + +Aplopus mayeri +Caudell + + +Paratype +; +Paratype +No. 42774 +U.S. +N.M. [USNM]; +PT +, ♀: Loggerhead Key, Dry +Tortugas +, Fla. [AMNH]; +PT +, ♀ (nymph): Loggerhead Key, Dry +Tortugas +, Fla. [AMNH]. +n. syn. +Werner, 1929: 9, figs. B (♂) & C (♀). Stockard, 1908a: 239ff, figs. (♀, 1st instar nymph & egg). Stockard, 1908b: 43, figs. (♂, ♀ & egg). Caudell & Hebard, 1912: 159. [Designation of +lectotype +] + +Rehn & Hebard, 1914: 101. + + +Arment, 2006: 18. + + + + +Haplopus mayeri +, Redtenbacher, 1908: 433 + +. + +Werner, 1929: 9, figs. + + +Otte & Brock, 2005: 152. + + + + +Haplopus evadne +, Caudell, 1904: 949 + +, figs. 1 & 2 (♀). [ +Misidentification +] + + + +Aplopus similis +Rehn, 1904: 65 + +. +HT +, ♂ (penultimate instar nymph): Swan Isl. Caribbean Sea; +U.S. +N.M. Acc. 19099, Cat. no. + +Aplopus similis +Rehn + +TYPE +; +Type +No.7343 +U.S. +N.M., wO192 [USNM], +PT +, ♀: acc 19099, Swan Isld., Caribbean Sea; Cat no. + +Aplopus similis +Rehn + +TYPE +; +Type +No. 7343 +U.S. +N.M. [USNM]. +n. syn. + +Diapherodes similis +, Moxey, 1972: 112 + +(in litt.). + +Haplopus similis +, Kirby, 1904a: 364 + +. + +Redtenbacher, 1908: 432. + + +Otte & Brock, 2005: 152. + + + +Further material [53 ♂♂, 44 ♀♀, 64 nymphs]: + + +DRY +TORTUGAS +: + + +16 ♂♂, 6 ♀♀, 10 ♂♂ (nymphs); 9 ♀♀ (nymphs): Loggerhead Key, Dry +Tortugas +, Fla., +July 8, 1912 +, R&H [ +ANSP +]; 1 ♀: + +Aplopus mayeri +Caudell, Loggerhead + +Key, Fla. [ +ANSP +]; 10 ♂♂, 7 ♀♀, 7 nymphs: Loggerhead Key, Dry +Tortugas +, FLA; R. E. Woodruff coll. +2.IX.61 +; At + +Suriana maritima + +L. [ +FSCA +]; 1 ♀: Dry +Tortugas +, +July 28, 1938 +, Jack Russel, No. 8271; + +Aplopus mayeri +Caudell + +, det. R. E. Woodruff—70 [ +FSCA +]; 22 ♂♂, 23 ♀♀, 31 nymphs (n4 to penultimate instar): +Tortugas +, FLA., Loggerhead Key, VII. [various dates] 1938, Jack Russell; + +Aplopus mayeri +Caud., Det. By T.N. Hubbell 1956 + +[ +UMMZ +]. + + +FLORIDA +KEYS +: + + +1 ♂ +(nymph n4): Key West, Fla. +July 3–7, 1912 +, leg. R & H [ +ANSP +]; 1 nymph (n2): Long Key, Fla. +July 13, 1912 +, R&H [ +ANSP +]; 1 nymph (n2): Key Largo, Florida, Monroe County, III, 18, 1910; + +A. mayeri +Caud., Hebard + +Collection [ +ANSP +]; 1 ♀: +Bahia, Honda, Fla. +, +VIII-14–38 +[ +ANSP +]; 1 ♀ (nymph—in Ryker mount): Key West Fla, +6.IV.03 +; EA Schwarz Collector; + +Aplopus mayeri +Caudell + +? ♀ nymph [ +USNM +]. + + +BAHAMAS +: + + +1 ♀: +Bahamas +, J. L. Bouchote, 1902.-299, coll. J. L. Bouchote, +Feb. 1902 +, Wood C. Andros, G. Smith [ +NHMUK +]; +1 ♂ +, 2 ♀♀: Nassau, N. P., +Bahamas +, Veronica Higgs!; + +Diapherodes scabricollis +Gray + +, det. C. F. Moxey 1972 [ +ANSP +]; 1 ♀: “Pink House”, on road, vic +FFS +, +WP +132, +13.V.03 +[ +ANSP +]; +1 ♂ +: +Bahamas +: Eleuthera, Rainbow Bay, I-VII-1988, R.W. & D.B. Wiley [ +FSCA +]; +1 ♂ +(penultimate instar), 1 ♀ (nymph n5): +Bahamas +: Andros Is., S. Fresh Creek nr. +U.S. +Naval Base; +26- VII-2006 +, Trevor Smith; beating [ +FSCA +]. + + + +NAVASSA +ISLAND + +: + + +1 ♂ +: +Navassa Island +; near lighthouse, +80 m +, +18°23.82’N +, +75°00.74’W +, +24 July 1998 +, Collrs. W. E. Steiner, J. M. Swearinger, +et al. +[ +USNM +]. + + +CAYMAN ISLANDS +: + + +1 ♂ +: Roy. Soc.-CIG Expdn. Little +Cayman +, BWI, North Shore track, N. Blossomvillage, +2.8.1975 +, R. R. Askew [ +NHMUK +]; +1 ♂ +: +17.IV.–26.VIII.1938 +, Oxf. Un. +Cayman +Is., Biol. Exped. Coll. By C. B. Lewis, G. H. Thompson, +2.VII.1938 +, Grand +Cayman +, East end of East end, Pres. Hope Dept. Oxford, B. M. 1967-147, East +End +Grand +Cayman +, +VII-2-38 +, 7238 J. [ +NHMUK +]; 1 ♀: +17.IV.–26.VIII.1938 +, Oxf. Un. +Cayman +Is., Biol. Exped. Coll. By C. B. Lewis, G. H. Thompson, +9.VII.1938 +, Grand +Cayman +, N. coast of North Side, G. C., +VII-9-38 +, 7938, Pres. Hope Dept. Oxford, B. M. 1967-147, + +Diapherodes pulverulentus +Gray + +det. Moxey 1972 [ +NHMUK +]; +1 ♂ +(nymph): +17.IV.–26.VIII.1938 +, Oxf. Un. +Cayman +Is., Biol. Exped. Coll. By C. B. Lewis, G. H. Thompson, +29.V.1938 +, Little +Cayman +, West end of S. W. Point area, Pres. Hope Dept. Oxford, B. M. 1967-147 [ +NHMUK +]. + + + + +Diagnosis: +This, the northernmost distributed representative of the genus, is easily distinguished from all other species in the genus by the very short alae of both sexes, which are considerably shorter than the tegmina ( +Fig. 269 +). The short alae of ♂♂ resemble + +H. brachypterus + + +n. sp. + +from Hispaniola and + +H. woodruffi + + +n. sp. + +from +Cayman +Brac ( +Cayman Islands +). From the first species ♂♂ clearly differ by: the more robust body; longitudinal white marking along the lateral margins of the pronotum ( +Fig. 266 +), and longitudinal white median markings on the median segment and abdominal tergites VIII–X; broader and less distinctly posteromedially indented anal segment ( +Fig. 242 +); differently shaped poculum ( +Fig. 275 +) and shorter terminal hook of the vomer ( +Fig. 353 +). From + +H. woodruffi + + +n. sp. + +they differ by: the more slender body; longitudinal white marking along the lateral margins of the pronotum ( +Fig. 266 +), and longitudinal white median markings on the median segment and abdominal tergites VIII–X; presence of a posterolateral tooth or lobe on abdominal tergum VII ( +Fig. 275 +); more slender three terminal abdominal segments ( +Fig. 275 +); longer and more flattened anal segment ( +Fig. 275 +); larger basal projection of the poculum ( +Fig. 274 +) and differently shaped vomer, which has the terminal hook considerably longer than in + +H. woodruffi + +( +Fig. 353 +). Females differ from those of + +H. woodruffi + + +n. sp. + +by: the acutely pointed and black-tipped horns of the head ( +Fig. 268 +); differently shaped anal segment and larger, shield-shaped epiproct ( +Fig. 273 +); ± decided sub-apical dorsal tooth of the meso- and metafemora and sub-basal dorsal tooth of the corresponding tibiae and gently rounded dorsal carina of the probasitarsus. + + + + +FIGURES 257–262. + +Haplopus scabricollis +Gray, 1835 + +. +257. +♀: Loggerhead Key (plain brown variety—dorsal view) [ANSP]; +258. +♀: Loggerhead Key (mottled variety—dorsal view) [ANSP]; +259. +♀: Loggerhead Key (plain brown variety—lateral view) [ANSP]; +260. +♀: Loggerhead Key (mottled variety—lateral view) [ANSP]; +261. +♂: Loggerhead Key (dorsal view) [ANSP]; +262. +♂: Loggerhead Key (lateral view) [ANSP]. + + + + +FIGURES 263–269. + +Haplopus scabricollis +Gray, 1835 + +. +263. +♂ (var.): Vanassa Island [USNM]; +264. +Head and pronotum of ♂ (var.) from Vanassa Island [USNM]; +265. +Tegmina and alae of ♂ (var.) from Vanassa Island [USNM]; +266. +Head and pronotum of ♂ from Eleutheria Island, Bahamas [FSCA]; +267. +Head and pronotum of ♂ from Loggerhead Key [ANSP]; +268. +Head and pronotum of ♀ from Loggerhead Key [ANSP]; +269. +Tegmina and alae of ♀ from Loggerhead Key [ANSP]. + + + + +FIGURES 270–275. + +Haplopus scabricollis +Gray, 1835 + +. +270. +Apex of abdomen of ♂ (var.) from Vanassa Island (lateral view) [USNM]; +271. +Apex of abdomen of ♂ (var.) from Vanassa Island (dorsal view) [USNM]; +272. +Apex of abdomen of ♀ from Loggerhead Key (lateral view) [ANSP]; +273. +Apex of abdomen of ♀ from Loggerhead Key (dorsal view) [ANSP]; +274. +Apex of abdomen of ♂ from Eleutheria Island, Bahamas (lateral view) [FSCA]; +275. +Apex of abdomen of ♂ from Loggerhead Key (dorsal view) [ANSP]. + + + + + +Description: ♀ ( +Figs. 257–260 +). + +Moderate to large (body length including the subgenital plate 125.0–164.0 mm) and moderately slender for the genus (maximum width of mesothorax 5.0–6.0 mm) with very short alae (5.3–8.0 mm); body surface very slightly glabrous. Colour variable and ranging from dark over mid and pale brown to pale grey; pale specimens are often all over furnished with mid to dark brown markings and speckles ( +Figs. 258, 260 +). Ventral body surface mostly with a yellowish or greenish wash. Head with one or two small elongate black markings above the eyes. Antennae greyish mid brown, sometimes with a slightly reddish hue. Eyes dark reddish brown. Spines of the thorax dark sepia with the points black. Tegmina and costal region of alae dark brown with the venations of a slightly paler colour; the latter black basally. Anal region of alae transparent pink and all major longitudinal and transverse veins marked with dark brown. + + +Head: About 1.4x longer than wide and ovoid with the cheeks slightly convex. Vertex very gently rounded and armed with a pair of moderately sized, pointed cephalad spines ( +Fig. 268 +). Behind these often with a further pair of tubercles. Eyes circular and contained about 2.5x in length of cheeks. Antennae reaching about half way along median segment. Scapus about +2x +longer than wide with the lateral margins gently rounded. Pedicellus roughly half the length of scapus and a little shorter than III. + + +Thorax: Pronotum longer but narrower than head, about +2x +longer than wide, roughly rectangular and with the lateral margins roundly emarginated medially. Transverse median sulcus faint, gently curved and not reaching lateral margins of segment. Dorsal surface with a pair of moderately sized, blunt spines in the +anterior +portion; otherwise with a variable number of small rather irregularly disposed spines ( +Fig. 268 +). Mesothorax about 2.4x longer than head and pronotum combined. Mesonotum very slightly gradually widened towards the posterior, the surface armed with a variable number of irregularly disposed spines or acute tubercles of variable sizes; usually a ± enlarged pair of spines is present in central portion. Lateral margins with a marginal row of about 8–12 small but pointed spines. Meso- and metapleurae armed with an irregular longitudinal marginal row of moderately sized spines. Mesosternum with a variable number of low spines or tubercles. Tegmina oval, coriaceous, with the venation very distinct, dense and irregularly disposed; hardly reaching to posterior margin of metanotum. The median protuberance very shallow and conspicuously displaced towards the apex of tegmen. Alae only 2/3 the length of tegmina and reaching only about 1/3 the way along median segment ( +Fig. 269 +). + + +Abdomen: Median segment about 1.8x longer than wide and very gently widened towards the posterior. All segments unarmed, except for a pair of retrorse and compressed posteromedian spines on tergites II–IV; this most prominent on II but sometimes poorly developed on all three segments. Segments II–VI roughly equal in length and width, all rectangular and about 1.8x longer than wide. Tergum VII slightly shorter and narrower than previous, about 2.2x longer than wide and slightly expanded posteriorly ( +Fig. 273 +). Praeopercular organ formed by a low, rounded swelling some distance off the posterior margin of sternum VII ( +Fig. 341 +). Tergum VIII slightly shorter than VII, narrowed anteriorly and roughly 2.5x longer than wide. IX slightly narrowed towards posterior and somewhat less than half the length of VIII. Anal segment with a very faint longitudinal median carina, narrowed in posterior half and with a very small triangular posteromedian incision. Epiproct of moderate size, roundly triangular and shield-shaped ( +Fig. 273 +). Cerci small and conical with a rather acute tip; slightly projecting over posterior margin of anal segment. Subgenital plate very long, lanceolate, longitudinally carinate and with a rather acute apex; extending over apex of abdomen by ± the combined length of tergites VIII–X ( +Figs. 272–273 +). + +Legs: Profemora about 4/5 the length of mesothorax, mesofemora ± reaching posterior margin of median segment and metafemora reaching about half way along abdominal segment IV. Profemora occasionally with two spines in the apical half of the medioventral carina, otherwise unarmed. Anteroventral carina of meso- and metafemora with two, posteroventral carina with one sub-apical spine; medioventral carina armed with 4–6 pointed spines. Both dorsal carinae with a ± distinct triangular tooth sub-apically. Anterodorsal carina of meso- and metatibiae with an angulate expansion sub-basally. Basitarsi roughly equal in length to following three tarsomeres combined; dorsal carina of probasitarsus gently rounded. + + +♂ ( +Figs. 261–262 +). + +Moderate to large (body length 83.0–121.0 mm) and fairly stocky (maximum width of mesothorax +2.8–3.1 mm +) for the genus with conspicuously shortened alae (length +4.2–6.2 mm +). Colouration variable and ranging from pale to mid greenish brown, the abdomen ranging from drab to dark brown. Ventral body surface green, the meso- and metapleurae green with a dull orange longitudinal stripe along lower margin. Head plain green but occasionally with a ± defined whitish postocular stripe. Dorsal spines of pro- and mesothorax mid brown with black tips. Lateral margins of pronotum and abdominal tergites II–IX broadly white. Median segment with a ± defined white longitudinal median stripe, often also with a white longitudinal median marking or stripe on abdominal tergites VII–X. Tegmina and costal region of alae dark brown, the latter black basally. Anal region of alae pink with all major veins brown. Antennae drab to pale brown. Tarsi mid brown. + + +Head: Generally as in ♀♀ but eyes more prominent, projecting hemispherically and their length contained only about +2x +in that of cheeks ( +Figs. 266–267 +). Antennae moderately robust and slightly projecting over abdominal segment II; with about 65 segments. + + +Thorax: Pronotum slightly longer but a little narrower than head, general shape as in ♀♀; surface smooth except for a moderate pair of spines in the +anterior +portion ( +Figs. 266–267 +). Mesothorax only about 2.0–2.1x longer than head and pronotum combined. Mesonotum with 5–16 irregularly disposed and paired spines of moderate size in the +anterior +2/3; the pair at +anterior +margin largest ( +Fig. 266–267 +). Mesosternum with ± ten and metasternum with two pairs of spiniform tubercles. Mesopleurae with a marginal row of granules, metapleurae smooth. Tegmina oval and very slightly projecting over posterior margin of metanotum, central protuberance very shallow. Alae small, shorter than alae and hardly reaching 1/3 the way along median segment. + + +Abdomen: Segment II a little shorter than III–IV and equal in length to V, about 2.5x longer than wide. IV longest segment and roughly 2.8x longer than wide. V–VII gradually decreasing in length with VII no more than 1.7x longer than wide. All tergites and sternites smooth. VII with a ± distinct, roundly triangular tooth posterolaterally ( +Fig. 275 +). VIII almost equal in length to VII and gently widening towards the posterior; IX slightly shorter than VIII and narrowed in posterior 2/3. Anal segment with a very faint longitudinal median carina in basal portion and gradually widened toward the posterior; the posterior margin broadly rounded with a very shallow median indentation ( +Fig. 275 +); slightly swollen and on ventral surface armed with several small, black incurving denticles. Epiproct very small and roughly triangular. Vomer with a fairly small, roughly semi-circular base and a long, papillate, up-curving terminal hook ( +Figs. 361–362 +). Cerci large, obtuse and about equal in length to anal segment. Poculum moderately convex, cup-like and with a fornicate basal hump ( +Fig. 274 +); posterior portion with a fine longitudinal median keel and somewhat indented medially ( +Figs. 361–362 +). + +Legs: Profemora roughly equal in length to mesothorax, mesofemora about ¾ the length of mesothorax and metafemora just not reaching posterior margin of abdominal segment IV. All less carinate than in ♀♀ but armature generally alike, except for the dorsal sub-apical teeth of the meso- and metafemora very distinct. Tarsi relatively more elongate and basitarsi a little longer than following three tarsomeres combined. + +Nymphs: +Immature ♀♀ usually have the retrorse posteromedian spines on abdominal tergites II–IV more prominent than adult insects and possess a well developed posterolateral tooth on tergum VII. Colour various shades of brown, grey and white. + + +Variability: +This very widely distributed species shows considerable variability in size, colouration (see description above), number and size of the thoracic spines and leg-armature. Specimens from +the Bahamas +on average are larger and somewhat more slender than specimens from the Florida Keys or Dry +Tortugas +, with ♂♂ usually longer than 90.0 mm and ♀♀ exceeding 140.0 mm including the subgenital plate. Furthermore, specimens from +the Bahamas +have the cephalad horns more acute and usually tipped with black (♀♀ in particular), whereas these are less developed, blunt and not tipped with black in ♀♀ from the Dry +Tortugas +or Florida Keys. Also the thoracic armature on average is more prominent in +the Bahamas +specimens with the pronotum usually bearing more than six spiniform tubercles to short spines. Examples from the +Cayman Islands +and Santanillas rather resemble specimens from +the Bahamas +in aspect of the cephalic and thoracic armature, having the cephalad horns distinct, acute and tipped with black and the prothoracic armature strongly developed. + + +A fairly small ♂ (body length +84.5 mm +) at hand from +Navassa +( +Fig. 263 +), a small island only some kilometres southwest off Hispaniola, differs from typical specimens of + +H. scabricollis + +from the Dry +Tortugas +, Florida Keys and +the Bahamas +by lacking distinct tubercles on the meso- and metasternum, entirely smooth meso- and metapleurae, lack of a posterolateral lobe or tooth on abdominal tergum VII ( +Fig. 271 +), less prominent basal projection of the poculum ( +Fig. 270 +); broader basal portion of the vomer ( +Fig. 354 +) and having only 56 antennomeres (roughly +65 in +typical + +scabricollis + +). Furthermore, the dorsal carinae of meso- and metafemora entirely lack a sub-apical tooth and there is also no sub-basal tooth on the anterodorsal carina of the corresponding tibiae. The lack of a posterolateral tooth on abdominal tergum VII and smooth dorsal carinae of the mid and hind legs resemble + +H. woodruffi + + +n. sp. + +from +Cayman +Brac ( +Cayman Islands +), but the acutely pointed and black tipped horns of the head ( +Fig. 264 +), white lateral margins of the pronotum ( +Fig. 264 +), white longitudinal median marking of the median segment, very short alae ( +Fig. 265 +) and morphology of the genitalia rather attribute it to + +H. scabricollis + +. However, more material from +Navassa Island +, including the unknown ♀ and egg, is required for any broader discussion on the identity of the present ♂. + + + + +Comments: +This species was first described by Gray (1835: 34) based on a ♂ and ♀ without locality now housed in the Linnean collection in London (LSUK). Both specimens were examined from detailed photographs kindly provided by Paul D. Brock (NHMUK) and in aspect of the large size (body lengths: ♂ +lectotype +121.0 mm, ♀ +paralectotype +164.0 mm including the subgenital plate; according to Redtenbacher, 1908: 432), acute and blacktipped cephalad horns and strong armature of the pronotum, most certainly are from +the Bahamas +. The ♀ +paralectotype +matches pretty well with a specimen from the island of Andros in NHMUK and the ♂ with a specimen from the island of Eleuthera in FSCA. Due to the strongly shortened alae, Gray (1835: 34) misinterpreted the ♂ to be a nymph, which is here selected as the +lectotype +of + +Diapherodes scabricollis + +in order to guarantee stability of the name and the new synonymy here established. + + +Examination of the +types +of + +Aplopus mayeri +Caudell, 1905 + +from Loggerhead Key in USNM leaves no doubt they are conspecific with Gray's + +scabricollis + +, hence Caudell's species is a junior synonym ( +n. syn. +). Two further +paralectotypes +, an adult ♀ which lacks the terminal three segments of the abdomen and a large ♀ nymph, are housed in AMNH. These are the specimens that had previously been described and figured by Caudell (1904: 949, figs. 1, 2) as + +H. evadne +Westwood, 1859 + +, a distinct species from Hispaniola. + + + +Haplopus similis +(Rehn, 1904) + +was described based on a ♀ and an immature ♂ from the Swan Islands (also Islas Santanilla or Islas del Cisne). Careful examination of these specimens show slight differences from typical + +H. scabricollis + +from the Dry +Tortugas +and Florida Keys. The prominent, acutely pointed and black-tipped cephalad horns and the prominently armed pronotum of the ♀ +paratype +resemble specimens from +the Bahamas +and +Cayman Islands +, but the specimen differs from + +H. scabricollis + +from all other localities by the more numerous spiniform tubercles of the mesonotum and meso- and metapleurae in particular, somewhat longer alae and having the praeopercular organ on abdominal sternum VII formed by two rough granules instead of one. The cephalic and thoracic armature are most certainly within the range of variability of + +H. scabricollis + +and the praeopercular organ may merely be an individual trait of this particular specimen. The immature ♂ +holotype +is not useful to distinguish it from + +H. scabricollis + +. Consequently, + +H. similis + +is here synonymised with + +H. scabricollis + +( +n. syn. +) although this synonymy deserves further evaluation by the availability of fresh material from this far off locality (see comments on distribution below). + + +This is the northernmost distributed representative of the entire Haplopodini, and the only species of + +Haplopus + +known to occur on +the Bahamas +, Florida Keys and even some localities near the coast on mainland Florida. This remarkable disjunct distribution appears obscure and warrants special mention and liekely explanation. + +H. scabricollis + +is distributed throughout the Dry +Tortugas +, Florida Keys and +Bahamas +but there are also apparently disjunct records from +Navassa +, a small island southeast off Hispaniola, the +Cayman Islands +and even as far southeast as the Swan Islands, a group of three small islands some +150 km +off the coastline of +Honduras +. Interestingly however, there have so far been no records from the coastlines of Hispaniola or +Cuba +. Since + +H. scabricollis + +is apparently restricted to coastlines and localities near the coast and is almost exceptionally peculiar to its main host-plant + +Suriana maritima +(Simarubaceae) + +, an occurrence in such habitats on Hispaniola and +Cuba +can not be fully excluded. The phasmatodean fauna of +Cuba +is still poorly prospected and perhaps this is also true for such habitats in eastern Hispaniola. + +Suriana maritima + +is a pantropic plant and found along coastlines throughout the entire Caribbean, including the +Cayman Islands +and Swan Islands and is also frequently found along the coasts of Central +America +. Since + +Suriana maritima + +is found on all the islands from which + +H. scabricollis + +has so far been recorded, a sufficient precondition is present for the occurrence of this species, a fact that is also true for +Cuba +and eastern Hispaniola. The coastal habitats of + +H. scabricollis + +may explain the wide and disjunct distribution of this particular species, since its distribution near the coast makes it prone to over-water dispersal on flotsam caused by frequent strong hurricanes within the Caribbean. + + +As shown by a large series of specimens + +H. scabricollis + +is apparently very abundant on Loggerhead Key of the Dry +Tortugas +(Stockard, 1908a: 239; 1908b: 43), e.g. the collection of UMMZ containing 22 ♂♂, 23 ♀♀ and 31 nymphs of various sizes all collected during a single month on Loggerhead Key. Rehn & Hebard (1914: 387) also reported it from Bird Key and Garden Key, the other islands of the +Tortugas +group, as well as Key West and Long Key. Rehn & Herbard (1912) furthermore recorded it from Key Largo, the Everglades and Dade County, Florida, which are the only records from the +United States +mainland. In the wild + +H. scabricollis + +is known to feed almost exclusively on bay cedar ( + +Suriana maritima + +, +Simaroubaceae +) and to be excellently camouflaged in these shrubs. Only a few specimens have so far been encountered on sea grape ( + +Coccoloba uvifera + +, +Polygonaceae +), which however is known to be eaten by these insects. Stockard (1908a, 1908b) provided detailed studies on the habitats, biology and behaviour of + +H. scabricollis + +(as + +Aplopus mayeri + +). + + + + +Distribution: +Dry +Tortugas +(Loggerhead Key [USNM]; Bird Key [Rehn & Hebard, 1914: 387]; Garden Key [Rehn & Hebard, 1914: 387]); Florida Keys (Key West [USNM]; Long Key [ANSP]; Key Largo [ANSP]; +Bahia Honda +Key [ANSP]; Big Pine Key [photo by Alejandro Lopez-Couto]; Key Biscane, Bill Baggs Cape Florida State Park [photo by Elizabeth Golden]); Florida (Miami Dade County [Rehn & Hebard, 1912: 243]; Everglades [Rehn & Hebard, 1912: 243]); +Bahamas +(South Bimini [AMNH]; Eleuthera [FSCA]; Nassau, New Providence [ANSP]; Andros [NHMUK]); +Cayman Islands +(Grand +Cayman +[NHMUK]; Little +Cayman +[NHMUK]) and Swan Islands [USNM]. + + + + +Number of specimens examined: +177 + + + +TABLE 25. +Measurements of + +Haplopus scabricollis +(Gray, 1835) + +[mm] + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
♀♀ Loggerhead Key♂♂ Loggerhead Key♀ Bahamas [NHMUK]♂ Bahamas [FSCA] +♂ +var. +Navassa Id. [USNM] + +♀, PT of + +similis + +[USNM]* +
Body (incl. sg. pl.)125.0–139.0-156.0--134.0
Body113.0–127.083.0–93.5141.094.384.5-
Pronotum--7.14.34.26.5
Mesonotum26.0–28.018.9–20.032.720.518.829.5
Metanotum6.8–8.05.1–6.09.85.85.07.5
Median segment7.3–8.26.0–6.99.16.26.49.5
Tegmina7.9–8.76.5–7.09.37.35.710.0
Alae5.3–6.54.2–5.06.05.23.910.0
Profemora Mesofemora17.8–20.0 15.5–17.018.8–20.0 15.0–16.024.4 20.417.9 15.319.3 17.521.5 18.7
Metafemora Protibiae21.0–22.0 -19.7–21.0 -26.5 26.020.0 18.821.4 19.624.5 22.5
+
+ +......continued on the next page + +
+
+
\ No newline at end of file diff --git a/data/38/7F/30/387F3068D3B1FF16FF27E8E226091B1F.xml b/data/38/7F/30/387F3068D3B1FF16FF27E8E226091B1F.xml new file mode 100644 index 00000000000..4124d31fc8e --- /dev/null +++ b/data/38/7F/30/387F3068D3B1FF16FF27E8E226091B1F.xml @@ -0,0 +1,269 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Haplopus woodruffi + +n. sp. + + + + +( +Figs. 279–286 +, +363 +) + + + + +HT, +♂: +Cayman Islands +: +Cayman +Brac, Bight Road at Maj. Donald Rd., +24-V-2009 +, coll.: R. H. Turnbow [FSCA]. +PT, +♂: +Cayman Islands +: +Cayman +Brac, Bight Road at Maj. Donald Rd., +24-V-2009 +, coll.: R. H. Turnbow [FSCA]. +PT, +♀: +Cayman Islands +: +Cayman +Brac, Bight Road at Maj. Donald Rd., +24-V-2009 +, coll.: M. C. Thomas [FSCA]. + + + + +Diagnosis: +Very close to + +H. scabricollis +(Gray, 1835) + +but differing by: the averagely smaller size; smaller and blunt horns of the head ( +Figs. 281–282 +); relatively larger eyes and lack of a sub-apical dorsal tooth on the meso- and metafemora; lack of a sub-basal tooth on the anterodorsal carina of the meso- and metatibiae; slightly longer tegmina and alae, the first distinctly projecting over the posterior margin of the metanotum and the latter in ♀♀ reaching about half way along the median segment with the anal region not distinctly red as in + +H. scabricollis + +. ♀♀ also differ by the slender probasitarsus, differently shaped anal segment and much smaller, triangular epiproct ( +Fig. 283 +). ♂♂ can be distinguished from those of + +H. scabricollis + +by: the lack of a white longitudinal marking along the lateral margins of the pronotum ( +Fig. 282 +) and median portion of the median segment; lack of a posterolateral tooth or lobe of abdominal tergum VII ( +Fig. 285 +); club-like, much more prominently swollen and broadened abdominal segments VIII–X ( +Fig. 285 +); shorter and dorsally globose anal segment ( +Fig. 286 +); smaller but conical basal projection of the poculum ( +Fig. 286 +) and differently shaped vomer, which has the terminal hook considerably shorter than in + +H. scabricollis + +( +Fig. 355 +). + + + + +Etymology: +This new species is dedicated to Dr. R. E. Woodruff (FSCA) for arranging loan of many specimens from the collection of FSCA and his private collection. + + + + + +Description: ♀ ( +Fig. 279 +). + +Of medium size (body length including the subgenital plate 142.0 mm) and moderately slender for the genus; body surface slightly glabrous. General colour creamish mid brown with faint darker speckles on body. Ventral body surface with a pale greyish wash. Head with two small, elongate black markings above the eyes. Cheeks irregularly furnished with white and dark brown ( +Fig. 281 +); two small black spots on frons. Antennae greyish straw, the apical portion with three dark transverse bands, otherwise about every fourth segment with a dark apex. Eyes pale ochraceous grey. Tubercles and spines of the thorax with black points. Tegmina and costal region of alae dark brown with the venations pale cream; the latter black basally. Anal region of alae transparent with a slight pinkish wash and all major longitudinal and transverse veins marked with black. + + +Head: About 1.3x longer than wide and ovoid with the cheeks moderately convex. Vertex rounded and armed with a pair of moderately sized, blunt and conical cephalad tubercles ( +Fig. 281 +). A further pair of small acute granules posteriorly. Eyes circular and contained about 1.8x in length of cheeks. Antennae almost reaching posterior margin of median segment; consisting of 61 segments. Scapus about +2x +longer than wide and slightly constricted towards the base. Pedicellus roughly half the length of scapus and 2/3 the length of III. + + +Thorax: Pronotum longer but narrower than head, almost +2x +longer than wide, roughly rectangular and with the lateral margins roundly emarginated medially. Transverse median sulcus rather decided, gently curved and not reaching lateral margins of segment. Dorsal surface with a two pairs of minute spines in the +anterior +portion and a pair of small spines near posterior margin; otherwise with a variable number of small rather irregularly disposed tubercles ( +Fig. 281 +). +Anterior +margin raised and with four spiniform tubercles. Mesothorax about 2.6x longer than head and pronotum combined. Mesonotum very slightly gradually widened towards the posterior and with a fine but acute longitudinal median carina; surface sparsely set with irregularly disposed small, spiniform tubercles and two pairs of small spines +in anterior +portion. Lateral margins with a marginal row of 10–12 spiniform tubercles. Meso- and metapleurae armed with an irregular longitudinal marginal row of small but pointed spines. Mesosternum with a few scattered granules and metasternum smooth except for two very small granules medially. Tegmina oval, coriaceous, with the venation very distinct, dense and irregularly disposed; reaching about ¼ along median segment. The median protuberance very shallow and conspicuously displaced towards the apex of tegmen. Alae a little shorter than tegmina and reaching only about half way along median segment. + + +Abdomen: Median segment about 1.7x longer than wide and very gently widened towards the posterior. All segments unarmed, except for a pair of small posteromedian spines on tergum II. Segments II–VI roughly equal in length and width, all rectangular and about +2x +longer than wide. Tergum VII slightly shorter and narrower than previous, about 2.2x longer than wide with lateral margins very slightly deflexed posteriorly. Praeopercular organ formed by a rounded sepia-coloured tubercle, which posteriorly extends into a longitudinal furrow, leaving a median gap in the posterior margin of sternum VII. Tergum VIII slightly shorter than VII, narrowed mediallly, almost +3x +longer than wide and 2.5x longer than IX. IX roughly rectangular. Anal segment with a very faint longitudinal median carina, the posterior margin slightly deflexed, broadly rounded and with a small posteromedian indentation. Epiproct very small, triangular ( +Fig. 283 +). Cerci very small, conical and with an acute tip; not reaching to posterior margin of anal segment. Subgenital palte very long, lanceolate, longitudinally keeled over entire length and with a narrow but rounded apex; extending over abdomen by almost the combined length of tergites VIII–X ( +Figs. 283–284 +). + +Legs: Profemora about 4/5 the length of mesothorax, mesofemora slightly projecting over posterior margin of median segment and metafemora reaching about half way along abdominal segment IV. Profemora unarmed. +Anteroventral carina of meso- and metafemora with two, posteroventral carina with one sub-apical spine; medioventral carina armed with 4–6 pointed and fairly strong spines. Both dorsal carinae of meso- and metafemora smooth but very gently elevated sub-apically. All tibiae unarmed. Basitarsi roughly equal in length to following three tarsomeres combined. + + +♂ ( +Fig. 280 +). + +Fairly small (body length 76.4–80.0 mm) and stocky for the genus with conspicuously shortened alae (length +4.7–5.5 mm +). General colour of dorsal body surface pale ochre with a greenish hue. Head, meso- and metapleurae, most of ventral body surface and legs green. Lateral margins of abdominal tergites II–VII each with a white +anterior +marking, largest on II and gradually decreasing in size towards VII ( +Fig. 280 +). Tergites VIII and IX with entire lateral margins broadly white and anal segment with a small white marking anterolaterally. Points of thoracal spines black. Eyes pale reddish brown, antennae ochre with a slight reddish wash in basal portion. Tegmina greenish cream in central portion with the +anterior +and posterior margins broadly white. Costal region of alae greenish cream interiorly, whitish anteriorly and black towards the base. Anal region transparent with a slight pinkish wash and all major longitudinal and transverse veins marked with dark black. Tarsi pale brown. + + +Head: Generally as in ♀♀ but eyes much more prominent, projecting hemispherically and their length contained only about 1.1x in that of cheeks. Vertex smooth except for the two small, blunt cephalad tubercles ( +Fig. 282 +). Antennae moderately robust and slightly projecting over abdominal segment II; otherwise as in ♀♀. + + +Thorax: Pronotum slightly longer and about as wide as head, general shape as in ♀♀; surface smooth except for one ( +paratype +) or two (holhotype, +Fig. 282 +) moderate pairs of spines in the +anterior +portion. Probasisternum smooth. Mesothorax about 2.4–2.5x longer than head and pronotum combined. Mesonotum with 6–8 paired spines of moderate size in the +anterior +2/3; the one ( +holotype +, +Fig. 282 +) or two ( +paratype +) pairs near +anterior +margin largest. Mesosternum smooth except for 2–4 green granules +in anterior +portion and occasionally a further small pair of granules medially; metasternum smooth. Mesopleurae with a few small granules +in anterior +portion, metapleurae smooth. Tegmina broadly oval and very slightly projecting over posterior margin of metanotum, central protuberance very shallow. Alae small, slightly shorter than alae and almost reaching half the way along median segment. + + +Abdomen: Segments II–V roughly equal in length and about 3.3x longer than wide. VI and VII decreasing in length with VII no more than 2.3x longer than wide; posterior portion of tergum VII very gently widened. All tergites and sternites smooth. Tergites VIII–X conspicuously swollen and about 1.7x broader than previous segments ( +Fig. 285 +). VIII about ¾ the length to VII, trapezoidal and strongly widening towards the posterior. IX about equal in length to VIII and gently narrowed towards the posterior. Anal segment shorter than IX, roundly rectangular with the dorsal surface roundly convex ( +Fig. 286 +). Posterior margin broadly rounded with a very shallow median indentation ( +Fig. 285 +); slightly swollen and on ventral surface armed with several small, black incurving denticles. Epiproct very small. Vomer with a broad base and a moderately elongate, conical, gently upcurving terminal hook which is about equal in length to basal portion ( +Fig. 363 +). Cerci large, obtuse and scarcely shorter than anal segment ( +Fig. 286 +). Poculum convex, cup-like with a small but acutely conical basal hump ( +Fig. 286 +). + + +Legs: Profemora scarcely shorter than mesothorax, mesofemora about 4/5 the length of mesothorax and metafemora reaching to +anterior +of abdominal segment V. All less carinate than in ♀♀ but armature generally alike. Tarsi relatively more elongate and basitarsi a little longer than following three tarsomeres combined. + + + + +Distribution: +Cayman Islands +( +Cayman +Brac: forest along Major Donald Drive) [FSCA]. + + + + +Number of specimens examined: +3 + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D3B4FF13FF27EDAF21F41B5E.xml b/data/38/7F/30/387F3068D3B4FF13FF27EDAF21F41B5E.xml new file mode 100644 index 00000000000..16763c8c6e2 --- /dev/null +++ b/data/38/7F/30/387F3068D3B4FF13FF27EDAF21F41B5E.xml @@ -0,0 +1,535 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +5.7. Genus + +Parhaplopus + +n. gen. + + + + +Type-species: + +Haplopus cubensis +Saussure, 1868: 68 + +, by present designation. + + + + + +Haplopus +, Westwood, 1859: 85 + +, pl. 18: 6, 6a & b (in part). Saussure, 1868: 68. + +Kirby, 1904a: 363, 364 (in part). +Redtenbacher, 1908: 429 (in part). Otte & Brock, 2005: 150 (in part). + + + +Description: ♂♂, ♀♀. +Large (body length ♀♀ +117.5–164.5 mm +, ♂♂ 78.0– +99.2 mm +), slender and elongate Haplopodini, ♀♀ brachypterous, ♂♂ with fully developed alae. Body sub-cylindrical (♀♀) or cylindrical (♂♂) in cross-section. Colouration of ♀♀ various shades of brown and grey. ♂♂ rather colourful insects, mostly green or greenish brown with body surface slightly glabrous. Head distinctly longer than wide, vertex very gently convex and moderately bi-spinose. Antennae moderately thickened; in ♀♀ reaching to median segment, in ♂♂ at least to abdominal segment II. Pronotum slightly shorter than the head, rectangular and sparsely tuberculose; entirely unarmed in ♂♂. Mesothorax moderately elongate and at best 2.3x longer than head and pronotum combined; parallel-sided in ♂♂ and medially swollen in ♀♀. Mesonotum of ♀♀ convex medially and rather irregularly armed with prominent, spiniform tubercles or blunt spines of various sizes; those in the raised central portion of the mesonotum largest and with a very broad base. Mesonotum of ♂♂ armed with 8–12 pointed spines. Mesopleurae with a longitudinal row of ± distinct tubercles and mesosternum irregularly granulose (♂♂) or minutely tuberculose (♀♀). Metasternum sparsely granulose in ♀♀ and smooth in ♂♂. Tegmina elongate, oval and with a moderately distinct central hump in ♂♂; reaching almost half way along median segment. Alae of ♀♀ indistinctly longer than tegmina; of ♂♂ well developed and reaching to abdominal segment VI. Anal region reticulate with distinct brown to black radial and transverse veins in ♀♀, translucent orange or pink with only the marginal portion slightly reticulate in ♂♂. Abdomen considerably longer than head and thorax combined. Median segment longer than metanotum, smooth. Segments II–VII distinctly longer than wide; II–VI ± rectangular. Tergites unarmed in ♂♂, II–IV sometimes with a ± distinct pair of posterior spines in ♀♀. VII with lateral margins ± rounded and elevated posteriorly (♀♀ in particular). VIII–X distinctly narrower (♀♀) or slightly wider (♂♂) than previous segments. Sternites II–VII smooth, except for a very few small granules on II–III of ♀♀. Praeopercular organ of ♀♀ indistinct and formed by a faint and short longitudinal median ridge close to posterior margin of sternum VII. Anal segment longitudinally carinate and the posterior margin with a small median notch; tapered in posterior portion in ♀♀. Epiproct very small, roundly triangular and almost completely hidden under anal segment in ♀♀. Vomer of ♂♂ prominent, broadly triangular and with a moderately long, acute terminal hook. Cerci very small, straight and tapered towards the pointed apex in ♀♀; obtuse, about 2/3 the length of anal segment and laterally compressed in ♂♂. Poculum of ♂♂ moderately convex, cup-like. Subgenital plate of ♀♀ very long, naviculate with the apex rounded or broadly truncate; projecting over apex of abdomen by at least the combined length of tergites VIII–X. Legs of moderate length, rather robust in ♀♀; pro- and mesofemora shorter (♀♀) or slightly longer (♂♂) than mesothorax. +Hind +legs ± reaching (♂♂) or clearly not reaching (♀♀) to the apex of abdomen. Two outer ventral carinae of meso- and metafemora each with 1–2 sub-apical spines and very minutely denticulose, the medioventral carina of these femora armed with a longitudinal row of five rather prominent spines. Dorsal carinae of all femora unarmed, those of the meso- and metafemora sometimes with a shallow sub-apical tooth in ♀♀. Tibiae unarmed except for a few small teeth in the apical portion of the medioventral carina; anterodorsal carina of ♀♀ undulate and lobate. Basitarsi of moderate length, longer than following two tarsomeres combined. Dorsal carina of probasitarsus with a rounded lobe. + + + +Eggs ( +Figs. 320–321 +): + +Of moderate size (capsule length +3.8 mm +), barrel-shaped and cylindrical in crosssection; capsule about +2x +longer than wide. In lateral aspect, dorsal surface of capsule considerably more convex than ventral surface. Polar-area impressed. Capsule surface strongly granulose and covered with irregular ridges. Micropylar plate small heart-shaped and <1/3 as long as capsule; posterior end with a wide median gap. Operculum flat, circular and in the centre with prominent, raised tubercles and hump-like projections; no conspicuous central capitulum. Colouration brown. + + + + + +Differentiation ( +Table 29 +): + +Very closely related and certainly the sister-taxon of + +Haplopus +Burmeister, 1838 + +. The eggs represent the most striking distinctive features, being barrel-shaped with the capsule surface distinctly tuberculose and covered with irregular ridges, the polar-area impressed and the operculum lacking the hat or knoblike extension seen in + +Haplopus + +. Adult insects may be distinguished by: the more elongate and distinctly less convex head, which merely bears two small cephalad spines or tubercles; medially swollen mesothorax; apically rounded or truncate subgenital plate and dorsally lobed probasitarsus of ♀♀; as well as the plain anal region of the alae and smaller, laterally compressed cerci ♂♂. For a detailed comparison and distinction from + +Haplopus + +see +Table 29 +below. + + +Comments: +The status of a subgenus of + +Haplopus +Burmeister, 1838 + +was originally considered for the three species here contained in + +Parhaplopus + + +n. gen. + +. In addition to a number of morphological characters of the insects the very distinctive eggs however appear to justify the status of + +Parhaplopus + +as a generic unit. Unfortunately, only a very few specimens are yet known. + + + + + +Distribution ( +Fig. 378 +): + +Cuba +, Gonaive +Island +and Hispaniola. + + + + +Etymology: +Masculine. A combination of the prefix “ +Par(a)- +“ (gr. = very similar) and the generic name + +Haplopus +Burmeister, 1838 + +to emphazise the close relation to this genus. + + + + + + + +Species included: + + + +1. + +Parhaplopus cubensis +(Saussure, 1868: 68) + +[ + +Haplopus + +]. +n. comb. +[Distribution: +Cuba +] + + +2. + +Parhaplopus evadne + +(Westwood, 1859: 85, pl. 18: 6, 6a & b (♂)) [ + +Haplopus + +]. +n. comb. +[Distribution: W-Hispaniola] + + +3. + +Parhaplopus navarroi + + +n. sp. + + + + +[Distribution: Hispaniola] + + + +TABLE 29. +Comparison and differentiation of + +Parhaplopus + + +n. gen. + +and + +Haplopus +Burmeister, 1838 + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+ +Parhaplopus + + + +Haplopus + +
+ +n. gen. + +
+Head +Longer than wide; vertex at best gentlyGlobose and indistinctly longer than wide;
rounded and armed with two smallvertex ± convex and distinctly bi-cornute
spines or tubercles
+
+ + +......continued on the next page + + + + +TABLE 29. +(Continued) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+ +Parhaplopus +n. gen. + + + +Haplopus + +
+Pronotum (♂♂) +Unarmed +With a ± distinct pair of +anterior +tubercles / spines +
+Mesothorax (♀♀) +Slightly swollen medially; armed with several large and blunt tuberclesSlender, not swollen medially; surface granulose or tuberculose
+Anal region of alae (♂♂) +PlainReticulate
+Cerci (♂♂) +Laterally compressed; apex narrowedCylindrical; apex rounded to club-like
+Poculum (♂♂) +Moderately convex; at best with a small hump basallyStrongly convex and with a ± distinct basal spine
+Subgenital plate (♀♀) +Apex rounded to broadly truncateApex narrow and ± pointed
+Probasitarsus (♀♀) +With a rounded dorsal lobeSlender
+Egg (capsule) +Barrel-shapedOvoid
+Egg (capsule surface) +Distinctly coriaceous / tuberculose and covered with irregular ridgesMinutely granulose / rugulose to almost smooth
+Egg (polar area) +ImpressedConvex and rounded
+Egg (micropylar plate) +Small; <1/3 the length of capsule> ½ the length of capsule
+Egg (operculum) +Flat and with an irregularly raised circular rim of tuberclesConvex, either conical or knob-like
+Keys to the species of + +Parhaplopus + +n. gen.
+
+ + +♀♀ + + + + +1. Subgenital plate naviculate to lanceolate with the apex bluntly rounded to pointed; Hispaniola......................... 2 + + + +- Subgenital plate gradually broadened towards a roundly truncate apex ( +Fig. 293 +); +Cuba +....................... + +cubensis + + + + + + + +2. Body length> 140.0 mm; cephalad horns prominent and acutely pointed ( +Fig. 303 +); pronotum multi-spinose ( +Fig. 303 +); mesonotum slender ( +Fig. 298 +); subgenital plate lanceolate with apex pointed ( +Fig. 308 +)......................... + +evadne + + + + + +- Body length +117.5 mm +; cephalad horns small, conical ( +Figs. 312–313 +); pronotum sparsely tuberculose ( +Fig. 312 +); mesonotum widened medially ( +Fig. 310 +); subgenital plate with apical half gently widened and apex bluntly rounded ( +Fig. 316 +).................................................................................................. + +navarroi + + +n. sp. + + + + + + +♂♂ + + + + + +1. Vertex with a pair of small spines; tegmina and costal region of alae green with a brown stripe along +anterior +margins...... 2 + + + + +- Cephalad spines prominent, conical ( +Figs. 301–302 +); tegmina and alae yellow with all longitudinal veins green ( +Fig. 298 +); His- paniola & Gonaive +Island +.......................................................................... + +evadne + + + + + + + +2. Head unicolourous ( +Fig. 297 +); abdominal tergum VII deflexed laterally; +Cuba +............................... + +cubensis + + + + + +- Cheeks white ( +Fig. 314 +); abdominal tergum VII parallel-sided; Hispaniola.............................. + +navarroi + + +n. sp. + + + + + + +
+
+
\ No newline at end of file diff --git a/data/38/7F/30/387F3068D3B6FF1FFF27E83626091FBF.xml b/data/38/7F/30/387F3068D3B6FF1FFF27E83626091FBF.xml new file mode 100644 index 00000000000..e366964df3c --- /dev/null +++ b/data/38/7F/30/387F3068D3B6FF1FFF27E83626091FBF.xml @@ -0,0 +1,312 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Parhaplopus cubensis +(Saussure, 1868) + +n. gen. +, n. comb. + + + + +( +Figs. 290–297 +, +344 +) + + + + + +Haplopus cubensis +Saussure, 1868: 68 + +. +HT +, ♀: +Cuba +; + +Haplopus cubensis +Sauss. + +[MHNG]. Saussure, +1871–1872 +: 192. + +Bolívar, 1888: 40. + +Kirby, 1904a: 364 (in part). +Redtenbacher, 1908: 433. +Otte & Brock, 2005: 151. + + + + +Aplopus cubensis +, Rehn, 1909: 200 + +(in part). + +Zompro & Brock, 2003: 10. + + +Diapherodes cubensis +, Moxey, 1972: 95 + +(in litt; in part—not ♀ from Turiguano, +Cuba +). [Description of ♂] + +Further material [ +1 ♂ +, 1 ♀]: + + + +CUBA +: + + + + + +1 ♀: Museum Paris, +Cuba +, La Havane, P. Serre 1910; + +Haplopus cubensis +Sauss., L. Chopard & L. Bertrand + +191 [MNHN]; +1 ♂ +: +Cuba +, Mr. H. d. Saussure; + +Haplopus evadne +Westw. + +[MHNG]. + + + + +Diagnosis: +Similar to + +P. navarroi + + +n. sp. + +from Hispaniola but differing by: the larger size and relatively longer mesothorax of both sexes; less distinct pair of tubercles on the vertex ( +Fig. 296 +); tuberculate abdominal segments; more decidedly posterolaterally expanded abdominal tergum VII ( +Fig. 293 +); broadly truncate apex of the subgenital plate ( +Fig. 293 +) and more undulate dorsal carinae of the protibiae of ♀♀. Males differ by the plain greenish brown head ( +Fig. 297 +) and more robust legs. + + + + + +Description: ♀ ( +Fig. 290–291 +). + +Large (body length including the subgenital plate +164.5 mm +) and characteristic for the broadly truncate apex of the subgenital plate. Colour greyish to ochraceous brown, with irregular pale grey mottling on dorsal surface of abdomen, meso- and metasternum. Metapleurae and ventral surface of abdomen pale greyish. Antennae pale brown dorsally and reddish mid brown ventrally. Eyes dull ochraceous. Spines of the thorax dull yellow to ochre, those of the mesonotum and pleurae with dark brown tips. Tegmina and costal region of alae greyish mid to dark brown with slight darker mottling in the basal and lateral portions; the venations ochre. Anal region of alae transparent drab and all major longitudinal and transverse veins broadly marked with dark brown. + + +Head: Ovoid, about 1.3x longer than wide; vertex gently convex and armed with a pair of small cephalad tubercles ( +Fig. 296 +); a few small tubercles present near posterior margin. Eyes fairly prominent, circular and contained slightly more than +2x +in length of cheeks. Antennae broken in both specimens available, but at least reaching to posterior of metanotum and consisting of> 50 segments. Scapus 2.2x longer than wide with the lateral margins gently rounded and slightly constricted towards the base. Pedicellus about half the length of scapus and longer than III, roughly cylindrical. + + +Thorax: Pronotum about equal in length but slightly narrower than head, 1.6x longer than wide, roughly rectangular and with the lateral margins gently emarginated medially. Transverse median sulcus distinct, gently curved and almost reaching lateral margins of segment. Dorsal surface with a pair of spiniform tubercles just in front of the median sulcus and in posterior portion with several small, irregularly disposed tubercles ( +Fig. 296 +). Probasisternum with a transverse row of four pointed tubercles. Profurcasternum with a few small tubercles along lateral margins. Mesothorax about 2.2x longer than head and pronotum combined, constricted at the +anterior +and conspicuously swollen medially. Mesonotum slightly widening towards the mid of segment, median portion swollen and in posterior portion almost parallel-sided. Surface with a fine longitudinal median carina and with a good number of very prominent, irregularly paired, conical spines of variable sizes; usually with two strongly enlarged pairs of spines +in anterior +half ( +Fig. 296 +). Along lateral margins with a marginal row of about 16 pointed spines. Mesopleurae armed with a longitudinal row of about 20 rather prominent and acute spines, metapleurae merely with a marginal row of eight tubercles. Mesosternum all over covered with irregularly disposed short spines, metasternum only with a few tubercles. Tegmina broadly ovate, coriaceous, with the venation very distinct, dense and irregularly disposed; roughly reaching to posterior margin of metanotum. The median protuberance very shallow. Alae a little longer than tegmina and reaching about 2/3 the way along median segment. + + +Abdomen: Median segment 1.8x longer than wide and very gently narrowed medially, in posterior portion with two small granules. Tergites II and III each with a few scattered tubercles, II–V with a transverse row of four tubercles along posterior margin and sternites II–IV each with a small median pair of tubercles; remaining segments unarmed. Segment II about 1.2x longer than median segment but shorter than III, rectangular and about 1.7x longer than wide. III–VI roughly equal in length and slightly longer than II, on average about 1.6x longer than wide. Tergum VII shorter and narrower than VI and about 1.7x longer than wide, lateral margins roundly deflexed posteriorly ( +Fig. 293 +). Sternum VII with the praeopercular organ formed by an elongate wart-like structure near posterior margin ( +Fig. 344 +). Tergum VIII about ¾ the length of VII, gently narrowed medially and roughly 1.4x longer than wide. IX almost rectangular and about half the length of VIII. Anal segment with a very faint longitudinal median carina, narrowed in posterior half and with a deep but narrow posteromedian emargination; epiproct very small ( +Fig. 295 +). Cerci very small and conical. Subgenital plate very long, naviculate, longitudinally carinate, gradually flattened and widened towards a broad and roundly truncate apex; extending over abdomen by more than the combined length of tergites VIII–X ( +Figs. 293–294 +). + + + +FIGURES 290–292. + +Parhaplopus cubensis +(Saussure, 1868) + +n. gen. +, n. comb.. +290. +♀: Cuba, Havanna [MNHN]; +291. +♀ HT: Cuba [MHNG]; +292. +♂: Cuba [MHNG]. + + + + +FIGURES 293–297. + +Parhaplopus cubensis +(Saussure, 1868) + +n. gen. +, n. comb.. +293. +♀ apex of abdomen: Cuba, Havana (dorsal view) [MNHN]; +294. +♀ apex of abdomen: Cuba, Havana (lateral view) [MNHN]; +295. +Anal segment and epiproct of ♀ HT (dorsal view) [MHNG]; +296. +Head, pro- and mesothorax of ♀ HT [MHNG]; +297. +Head and pronotum of ♂ [MHNG]. + + +Legs: Profemora about 3/5, mesofemora about 2/3 the length of mesothorax and metafemora just not reaching posterior margin of abdominal segment III. Medioventral carina of profemora with 7–9 small spines, in meso- and metafemora armed with five very prominent and strong, back-curving spines. Anterodorsal carina of profemora strongly raised and slightly undulate, the anterodorsal carina of the protibiae lamellate and furnished with four rounded lobes. Anteroventral carina of meso- and metafemora with two, posteroventral carina with one strong subapical spine; both carinae minutely granulose. Both dorsal carinae with a slight triangular lobe-like tooth subapically. Anterodorsal carina of meso- and metatibiae with a roundly triangular elevation sub-basally and subapically. Probasitarsus about as long as the following two tarsomeres combined, dorsal carina rounded. Meso- and metabasitarsi simple and just a little longer than 2nd tarsomere. + + +♂ ( +Fig. 292 +). + +Unfortunately, the terminal abdominal segments are broken off and missing in the only specimen available. Of moderate size and fairly slender for the genus. Colour greenish brown, the posterior portion of the pronotum and bases of the profemora dull green. Ventral surface of body and profemora mostly whitish to pale grey with darker speckles, metapleurae green. Cheeks with a slight dark brown wash ( +Fig. 297 +). Apices of all femora mid brown. Dorsal spines of pro- and mesothorax with black tips, those of the mesopleurae and sternum dark olive. Tegmina and costal region of alae with +anterior +margin white, then a broad brown longitudinal band, and innermost portion green. Anal region of alae pale transparent pink with a slight greyish hue along the outer margin. Antennae dark ochracheous with a few dark brown transverse bands, tarsi pale brown. + + +Head: Generally as in ♀♀ but vertex flattened and smooth except for two small cephalad spines ( +Fig. 297 +); eyes much more prominent, projecting hemispherically and their length contained only about 1.8x in that of cheeks. Antennae moderately robust and projecting over posterior margin of median segment; consisting of 61 segments. Otherwise as in ♀♀. + + +Thorax: Pronotum slightly shorter and narrower than head with the lateral margins gently concave medially; surface smooth ( +Fig. 297 +). Transverse median sulcus shallow, gently rounded and just not reaching lateral margins of segment. Probasisternum with a small median pair of granules. Mesothorax about 1.9x longer than head and pronotum combined. Mesonotum armed with about ten distinct paired spines in the +anterior +2/3. Mesopleurae with a longitudinal row of acute tubercles, metapleurae only with a few small granules. Mesosternum with numerous irregular low spiniform tubercles; metasternum smooth. Tegmina oval and reaching about ¼ the way along median segment, central protuberance roundly conical. Alae almost reaching to posterior margin of abdominal segment VI (46.0 mm). + + +Abdomen: Segments II-V roughly equal in length and about 3.6x longer than wide; all unarmed. VI slightly shorter than previous and hardly +3x +longer than wide. Remaining segments missing in the unique specimen available. + +Legs: Legs all fairly short and moderately robust. Profemora very slightly longer, and mesofemora a little shorter than mesothorax, metafemora projecting a little over posterior margin of abdominal segment III. All less carinate than in ♀♀ and lacking any dorsal elevations or teeth. Armature of medioventral carina of the femora as in ♀♀ but considerably less developed. Tarsi relatively more elongate, probasitarsus almost equal in length to following three tarsomeres combined, meso- and metabasitarsus about as long as combined length of following two segments. Dorsal carina of probasitarsus gently rounded. + + + +Comments: +Brief examination of the ♀ recorded by Moxey (1971: 95, in litt.) from +Isla +de Turiguano in ANSP has shown this to be a distinct species, hence this is an erroneous record (→ + +Haplopus sobrinus + + +n. sp. + +). Eggs unknown. + + + + +Distribution: +Cuba +(Camagüey & Oriente, Santiago de +Cuba +[USNM; Moxey, 1972: 97, in litt.]); NW- +Cuba +(Havanna) [MNHN]. + + + + +Number of specimens examined: +3 + + + + \ No newline at end of file diff --git a/data/38/7F/30/387F3068D3BAFF1BFF27E8FF26091A93.xml b/data/38/7F/30/387F3068D3BAFF1BFF27E8FF26091A93.xml new file mode 100644 index 00000000000..c58542c2f23 --- /dev/null +++ b/data/38/7F/30/387F3068D3BAFF1BFF27E8FF26091A93.xml @@ -0,0 +1,421 @@ + + + +Studies on Neotropical Phasmatodea XVI: Revision of Haplopodini Günther, 1953 (rev. stat.), with notes on the subfamily Cladomorphinae Bradley & Galil, 1977 and the descriptions of a new tribe, four new genera and nine new species (Phasmatodea: “ Anareolatae ”: Phasmatidae: Cladomorphinae) + + + +Author + +Frank H. Hennemann + + + +Author + +Oskar V. Conle + + + +Author + +Daniel E. Perez-Gelabert + +text + + +Zootaxa + + +2016 + +4128 + + +1 + + +1 +211 + + + +journal article +38706 +10.11646/zootaxa.4128.1.1 +553faca2-0799-4bbe-8b54-92960421d9c9 +1175-5326 +271800 +B4D2CD84-8994-4CEF-B647-3539C16B6502 + + + + + + + +Parhaplopus evadne +(Westwood, 1859) + +n. gen. +, n. comb. + + + + +( +Figs. 298–309 +, +355 +, +379–398 +) + + + + + +Haplopus evadne +Westwood, 1859: 85 + +, pl. 18: 6, 6a & b (♂). +HT +, ♂: +Type +, St. Dom. 55.1., + +Haplopus Evadne +Westw., St. +Domingo + +, + +evadne +Westw. Mon. Phasm. Pl. + +18 fig. 6, + +Haplopus evadne +Westwood + +, HT; BMNH(E) #844943 [NHMUK]. Brock +et al. +, (in press) + +Kirby, 1904a: 363. + + +Redtenbacher, 1908: 432. +Otte & Brock, 2005: 151. + + + + +Diapherodes evadne +, Moxey, 1972: 97 + +(in litt.). + + +[ +Not: + +Haplopus evadne +Caudell, 1904: 949 + +, figs. 1 & 2 (♀)— +misidentification +. Later described as + +Aplopus mayeri +Caudell, 1905 + += + +A. scabricollis +(Gray, 1835) + +] + + + + +Further material [6 ♂♂, 1 ♀]: +HISPANIOLA ( +HAITI +): + + +1 ♂ +: Gonaive Is., +Haiti +, Aug., Eyerdam coll.; wO130 [ +ANSP +]; +1 ♂ +: +Haiti +: Dept. Sud'est, Formond, alrededores Kay, Michel 2026684 mN, 603254 mE, +1100 m +, +4–8 February 2006 +, coll. R. Bastardo; 33514 ( +MHND +) [ +USNM +]; 1 ♀: +Haiti +: Department du Sud, Formon, alrededores de Kay Michel, +1100 m +, 603254 mE, 2026684 mN, +9.II.2006 +, R. Bastardo; 35424 ( +MHND +) [ +USNM +]; +1 ♂ +: +Haiti +: Department du Sud, Formon, alrededores de Kay Michel, +1100 m +, 603254 mE, 2026684 mN, +9.II.2006 +, R. Bastardo; 35403 ( +MHND +) [ +USNM +]; +1 ♂ +: +Haiti +: Department du Sud, Formon, alrededores de Kay Michel, +1100 m +, 603254 mE, 2026684 mN, +9.II.2006 +, R. Bastardo; 38600 ( +MHND +) [ +USNM +]; +1 ♂ +: +Haiti +: Department du Sud, Formon, alrededores de Kay Michel, +1100 m +, 603254 mE, 2026684 mN, +9.II.2006 +, R. Bastardo; 33594 ( +MHND +) [ +USNM +]; +1 ♂ +: +Haiti +: Department du Sud, Formon, alrededores de Kay Michel, +1100 m +, 603254 mE, 2026684 mN, +9.II.2006 +, R. Bastardo; 35484 ( +MHND +) [ +USNM +]. + + + + +Diagnosis: +Males readily differ from the other two species in the genus by: the large size; much more prominent cephalad horns; pale green colouration and yellow tegmina and alae which have all longitudinal veins broadly marked with bright green. Females resemble those of +P. n av a r roi + +n. sp. + +but differ by: the larger size; much more prominent cephalad horns; more prominently spinose pronotum and mesothorax; more decided spines of the metapleurae; larger, semi-circular and shield-shaped epiproct and slender apically pointed subgenital plate. + + + + +Description: +The colouration is described from photos of live specimens taken at Parc National Pic Macaya, Massif de la Hotte. + + + +♀ ( +Fig. 298 +). + +Fairly large (body length including the subgenital plate 149.0 mm) and fairly slender for the genus. Colour greenish mid brown all over mottled with irregular dark brown markings. Abdominal tergites III–VI with a pale cream roughly square marking anteriorly. Legs dull greenish brown. Entire thoracic armature tipped with black. Antennae dark reddish to greenish brown with most antennomeres, except for the scapus, dull brown to black apically. Eyes cream with reddish brown mottling. Tegmina and costal region of alae dull ochraceous with faint darker mottling. Anal region of alae transparent grey with all major longitudinal and transverse veins broadly marked with black. + + +Head: Ovoid, about 1.3x longer than wide; vertex gently convex and armed with a pair of fairly large conical, apically pointed and black tipped cephalad horns; the dextral one bifid in the only specimen at hand. A further pair of spiniform tubercles towards the frons and two pairs of low spiniform tubercles in the posterior portion. Cheeks with two small granules ( +Fig. 303 +). Eyes rather small, circular in outline and contained almost 2.5x in length of cheeks. Antennae reaching about half way along median segment. Scapus some 1.5x longer than wide with the lateral margins gently rounded. Pedicellus less than half the length of scapus and about equal in length to III, roughly cylindrical. + + +Thorax: Pronotum slightly longer and somewhat narrower than head, 1.6x longer than wide, roughly rectangular and with the lateral margins very gently emarginated medially ( +Fig. 303 +). Transverse median sulcus distinct, gently curved and almost expanding over entire width of segment. +Anterior +portion with two pairs of blunt spines, the +anterior +pair being larger and more distant than the posterior pair; a further pair of small spiniform tubercles on +anterior +margin. Posterior half with ten almost equally sized paired spines. Profurcasternum with two black-tipped spiniform tubercles at lateral margins and two tubercles near posterior margin. Mesothorax about 2.2x longer than head and pronotum combined, slender and somewhat constricted in the +anterior +portion. Mesonotum all over armed with numerous spines of variable sizes and a longitudinal row of about 12 pointed spines along lateral margins. Mesopleurae armed with a longitudinal row of about 16 medium sized spines and metapleurae with a marginal row of about 8–9 short spines. Mesosternum with roughly 12 fairly distinct spiniform tubercles and the metasternum sparsely tuberculose. Tegmina broadly ovate, coriaceous, with the venation very distinct, dense and irregularly disposed; slightly projecting posterior margin of metanotum; the median protuberance shallow. Alae some 1.3x longer than tegmina and almost reaching to posterior margin of median segment. + + + +FIGURES 298–300. + +Parhaplopus evadne +(Westwood, 1859) + +n. comb +.. +298. +♀: Haiti, Department du Sud, Formon [USNM]; +299. +♂ Haiti, Department du Sud, Formon [USNM]; +300. +♂ HT: Dominican Republic, Santo Domingo [NHMUK]. + + + +Abdomen: Median segment 1.6x longer than wide and roughly rectangular, surface smooth. Tergites I–IV each with posteromedian pair of small retrorse spines, which are most prominent on II; remaining segments unarmed. Segments II–VII roughly equal in length and about 1.3x longer than wide. II–III somewhat widening, IV roughly parallel-sided and V–VII very slightly but gradually narrowing. Tergum VII with the lateral margins very gently rounded ( +Fig. 308 +). Sternum II with a pair of granules posteromedially, remaining sterna smooth. Praeopercular organ formed by a shallow, longitudinal median granule in posterior portion of sternum VII ( +Fig. 309 +). Tergum VIII somewhat less than ¾ the length of VII and roughly 1.5x longer than wide. IX almost rectangular and about half the length of VIII. Anal segment parallel-sided with posterior portion narrowed and the posterior margin with aconcave median emargination; epiproct small almost semi-circular and shield-shaped with a fine longitudinal median carina ( +Fig. 308 +). Cerci very small, conical and scutely pointed; hardly projecting over posterior margin of anal segment. Subgenital plate very long, naviculate, longitudinally carinate and gradually narrowing towards an acute apex; extending over abdomen by more than the combined length of tergites VIII–X ( +Figs. 307–309 +). + + + +FIGURES 301–309. + +Parhaplopus evadne +(Westwood, 1859) + +n. comb +.. +301. +Head and pronotum of ♂ HT (lateral view) [NHMUK], +302. +Head and pronotum of ♂ Haiti, Department du Sud, Formon [USNM]; +303. +Head and pronotum of ♀ Haiti, Department du Sud, Formon [USNM]; +304. +♂ apex of abdomen: Haiti, Department du Sud, Formon (lateral view) [USNM]; +305. +♂ apex of abdomen: Haiti, Department du Sud, Formon (ldorsal view) [USNM]; +306. +♂ apex of abdomen: Haiti, Department du Sud, Formon (ventral view) [USNM]; +307. +♀ apex of abdomen: Haiti, Department du Sud, Formon (lateral view) [USNM]; +308. +♀ apex of abdomen: Haiti, Department du Sud, Formon (ldorsal view) [USNM]; +309. +♀ apex of abdomen: Haiti, Department du Sud, Formon (ventral view) [USNM]; + + +Legs: Pro- and mesofemora shorter than mesothorax and metafemora almost reaching half way along abdominal segment III. Medioventral carina of profemora with six small spines, in mesofemora armed with four and on metafemora with five rather prominent spines. Anterodorsal carina of profemora and tibiae strongly raised, the latter slightly undulate. Anteroventral carina of meso- and metafemora with two, the posteroventral carina with one sub-apical spine. Both dorsal carinae slighty elevated sub-apically. Anterodorsal carina of mesotibiae gently rounded sub-basally and sub-apically. Probasitarsus about as long as the following three tarsomeres combined, the dorsal carina gently rounded. Meso- and metabasitarsi simple and slightly shorter than following three tarsomeres combined. + + +♂ ( +Figs. 299–300 +, +379–398 +). + +Large (body length 89.0– +99.2 mm +) and fairly slender for the genus with well developed alae (length>36.0–49.0 mm). Colour of body and legs pale yellowish green, the mesonotum, metanotum and three basal abdominal tergites pale creamish brown; body surface slightly glabrous. Cheeks with a faint yellow postocular stripe, eyes pale creamish brown and the antennae drab to pale ochraceous. All spines of thorax with black tips. Metapleurae with a white longitudinal stripe along upper margin and lateral margins of abdominal tergites VIII and IX broadly yellow. Cerci cream to pale brown and greenish basally. Tegmina and costal region of alae bright yellow with five bright green longitudinal streaks along the main veins. Anal region of alae plain transparent orange. Tarsi pale greenish brown. + + +Head: Ovoid and about 1.3x longer than wide, vertex slightly convex and armed with a pair of obtuse tubercles to acutely pointed spines; usually two small granules behind these ( +Figs. 301–302 +). Eyes sub-circular, projecting hemispherically and their length contained less than +2x +in that of cheeks. Antennae moderately robust and reaching to +anterior +of abdominal segment III; consisting of about 56 segments. + + +Thorax: Pronotum about equal in length but narrower than head, roughly rectangular and with the lateral margins gently concave; surface smooth ( +Figs. 301–302 +). Transverse median depression moderately distinct, slightly rounded and not reaching lateral margins of segment. Mesothorax about 2.3x longer than head and pronotum combined. Mesonotum armed with 9–12 rather distinct, obtusely conical spines which are roughly arranged in two longitudinal rows along +anterior +2/3 of dorsal surface; either black-tipped or almost completely black. Mesopleurae with a longitudinal row a minute granules, metapleurae unarmed. Mesosternum with about four low spines +in anterior +portion and a few small tubercles behind; metasternum smooth. Tegmina oval and reaching about 1/3 along median segment, central protuberance rather distinct, roundly conical and positioned premedially. Alae very long and projecting over posterior margin of abdominal segment V. + + +Abdomen: Segments II–IV roughly of equal length and about +4x +longer than wide. V–VII gradually decreasing in length with VII only about ¾ the length of II–IV and no more than 3.5x longer than wide. All tergites and sternites smooth, tergites II–VII parallel-sided. VIII about 3/5 the length of VII and gradually widening towards the posterior; IX very slightly shorter than VIII and narrowed towards the posterior. Anal segment with a faint longitudinal median carina, slightly converging towards the posterior and posterior margin with a roundly triangular median emargination ( +Fig. 305 +); on ventral surface armed with several small, black in-curving denticles. Epiproct very small and fully concealed by anal segment. Vomer with a broad and rounded base and a short but acutely pointed terminal hook ( +Fig. 355 +). Cerci elongate, a little longer than anal segment, laterally compressed, carinate dorsally and ventrally ( +Fig. 355 +) and gradually constricted towards a narrow apex ( +Figs. 304–306 +). Poculum moderately convex, scoop-like and with a small, rounded tubercle at the base ( +Fig. 304 +); posterior portion longitudinally carinate and the posterior margin indented medially ( +Fig. 355 +). + +Legs: Profemora a little longer and mesofemora slightly shorter than mesothorax, metafemora reaching about 2/3 the way along abdominal segment IV. Medioventral carina of profemora with three small spines in apical portion, of meso- and metafemora armed with five strong spines. Anteroventral carina of meso- and metafemora with two, the posteroventral carina with one sub-apical spine. Basitarsi a little longer than following three tarsomeres combined. + +Variability: +Males show variability in the number and size of the mesothoracal spines as well as the size and shape of the cephalad horns. The mesonotal spines range from +9–12 in +number and are mostly black-tipped but may be almost completely black in specimens which have them strongly developed. The cephalad horns are rather blunt and conical in shape ( +Fig. 301 +) but in some specimens at hand are prominent, elongate and acutely pointed with the tip if the dextral horn black ( +Fig. 302 +). + + + + +Comments: +Westwood (1859: 85, pl. 18: 6) originally described and illustrated this species based on a unique ♂ from Santo +Domingo +( +Dominican Republic +) in NHMUK. Eggs unknown. + + + + + +Distribution ( +Fig. 379 +): + +Hispaniola. +Dominican Republic +: Santo +Domingo +[NHMUK]; Departamento de Vida Silvestre [photograph taken by Eladio Fernández]. SE-Haiti: Parc National Pic Macaya, Massif de la Hotte, Formon, alrededores de Kay Michel +1100 m +[USNM]. Gonaive +Island +[ANSP]. + + + + +Number of specimens examined: +8 + + + + \ No newline at end of file diff --git a/data/38/7F/7D/387F7D471329E8FD27717BD902566E50.xml b/data/38/7F/7D/387F7D471329E8FD27717BD902566E50.xml new file mode 100644 index 00000000000..9c467c29091 --- /dev/null +++ b/data/38/7F/7D/387F7D471329E8FD27717BD902566E50.xml @@ -0,0 +1,50 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828--9042 + + + + + +Stibeutes heinemanni +Foerster +, 1850 + + + + +Distribution +England, Scotland + + + \ No newline at end of file diff --git a/data/38/7F/E0/387FE0251D78D74CCAEE832F2925AB45.xml b/data/38/7F/E0/387FE0251D78D74CCAEE832F2925AB45.xml new file mode 100644 index 00000000000..86915ccc7f5 --- /dev/null +++ b/data/38/7F/E0/387FE0251D78D74CCAEE832F2925AB45.xml @@ -0,0 +1,70 @@ + + + +Die Milbenfauna der Nordseeinsel Wangerooge + + + +Author + +Willmann, C. + +text + + +Veröffentlichungen des Instituts für Meeresforschung Bremerhaven + + +1952 + +1 + + +139 +186 + + + + +http://unknown + +journal article +ORI11037 + + + + +2. +Eugamasus trouessarti +Berlese & Trouessart 1889. + + + + +Fundorte: Die Spezies wurde festgestellt in sieben verschiedenen Proben im +Aussengroden +der Insel meist im Salicornietum, und zwar: +Aussengroden-Sued +, 19. VI. 49 - Vogelschutzgebiet-Ost, Bodenprobe mit +Salicornia +, 9. X. 49 - +Aussengroden-Sued +, 8. X. 49, - 6. X. 49 - Deich, Wattseite, unten am +Fusse +des Deiches, 17. 1. 50. + + + + +Die +Species ist neu +fuer +die deutsche +Kueste +. Sie ist bekannt aus Frankreich, Irland und Norwegen, wo sie ebenfalls an der +Kueste +innerhalb der Gezeitenzone verbreitet ist. + + + + \ No newline at end of file diff --git a/data/38/80/3B/38803BF77B5FC82CAEBE5F12856DB562.xml b/data/38/80/3B/38803BF77B5FC82CAEBE5F12856DB562.xml new file mode 100644 index 00000000000..0ee7217f292 --- /dev/null +++ b/data/38/80/3B/38803BF77B5FC82CAEBE5F12856DB562.xml @@ -0,0 +1,153 @@ + + + +Two new species of Dacne Latreille (Coleoptera, Erotylidae) from China, with a key to Chinese species and subspecies of Dacne + + + +Author + +Dai, Cong-Chao + + + +Author + +Zhao, Mei-Jun + +text + + +ZooKeys + + +2013 + +261 + + +51 +59 + + + + +http://dx.doi.org/10.3897/zookeys.261.4495 + +journal article +http://dx.doi.org/10.3897/zookeys.261.4495 +1313-2970-261-51 + + + + +Dacne (Xenodacne) hujiayaoi Dai & Zhao +sp. n. +Figs. 10, 11 +12-15 +17 + + + +Type material. + +Holotype:CHINA: Yunnan Prov.: ♂, Nabanhe N.R., Bengganghan, Nanmugahe, +22°06'N +, +100°27'E +, alt. 1700 m, 13.XI.2008, H Jia-Yao & TANG Liang leg. (SHNU). + + + + +Description +. + +Body (Fig. 10, 11) stout, elongate, length: 3.6 mm; width: 1.5 mm. Body black; legs, palpi and base of antennae reddish-brown; antennal club dark brown. Each elytron with one orange band. + +Head width between eyes = 3.5 times eye diameter in dorsal view; punctation coarse, separated by 1-3 puncture diameters; epistome truncate, lacking marginal line on anterior margin; stridulatory files not evident. Antennae (Fig. 15) long, extending behind posterior border of pronotum; antennomere III about 1.2 times as long as IV; antennomere VIII slightly wider than VII, about 1.5 times as wide as long; antennomere IX trapezoidal; antennomere X transverse; antennomere XI almost elliptic; relative lengths of antennomeres +II-XI +: 9.0: 11.5: 8.0: 8.0: 8.0: 8.0: 7.5: 10.0: 10.0: 17.0. Maxillary and labial terminal palpomeres acuminate, sensory area restricted to apex. Mentum broad with anterior projection, almost triangular, slightly more than 1.5 times wider than long. + + +Pronotum arched, widest at base (pl/pw = 0.62); slightly narrowing toward apex; lateral margin thickened anteriorly; pronotal anterior margin normal, not projecting forward beyond anterior angles (typical for the subgenus +Xenodacne +). Pronotum distinctly punctured medially, finely and closely punctured laterally. + + +Prosternum with anterior edge straight, lacking marginal bead; posterior process broad, width more than diameter of procoxa; prosternal lines apparently lacking; punctures coarse and close, diameter = eye facet, separated by 0.5-1.0 puncture diameters. +Abdomen +with distinct coxal lines on first ventrite nearly attaining posterior margin. Legs with tibia not dilated at apex. + +Scutellum pentagonal, finely and sparely punctured. +Elytra margined basally; widest at middle, then gradually narrowing to apex; with fine punctures. + +Male +genitalia (Fig. 12, 14) moderately curved; median lobe short, apically pointed; median strut long, about 1.6 times as long as median lobe. Tegmen with parameres long, flattened, tightly fitting basal piece and each other. Internal sac simple (Fig. 13). + + + +Distribution. +China (Yunnan Province). + + +Diagnosis. + +Dacne hujiayaoi +is most similar to +Dacne (Xenodacne) zonaria +Lewis and +it's +subspecies due to similar form and color pattern of the body. +Dacne hujiayaoi +can be distinguished from +Dacne zonaria +by body indistinctly shining, eyes large (head width between eyes = 3.5 times eye diameter in dorsal view), the reddish-brown legs and occurs in southwest China. +Dacne zonaria +has the body distinctly shining, eyes small (head width between eyes> 4 times eye diameter in dorsal view), the black legs and occurs in Japan, Korea, Siberia and Taiwan ( + +Chujo +and +Chujo +1988 + +). + + + +Etymology. +This species is named in honor of Mr. Jia-Yao Hu, collector of the new species and teacher of the senior author. + + +Figures 10-11. Habitus of +Dacne (Xenodacne) hujiayaoi +in dorsal and ventral view. Scale = 1 mm. + + + + +Figures 12-15. +Dacne (Xenodacne) hujiayaoi +. 12, 14 aedeagus in lateral views 13 internal sac and flagellum in dorsal view 15 antenna. Scales = 0.05 mm(13), Scales = 0.2 mm(12, 14, 15). + + + + +Figures 16-19. Habitus of Chinese species of +Dacne +in dorsal view ( +Dacne zonaria taiwana +is excluded). 16 +Dacne (Dacne) japonica +17 +Dacne (Xenodacne) hujiayaoi +18 +Dacne (Dacne) picta +19 +Dacne (Xenodacne) tangliangi +. Scale = 2 mm. + + + + + \ No newline at end of file diff --git a/data/38/80/62/38806286906549243109D7179D3FD12B.xml b/data/38/80/62/38806286906549243109D7179D3FD12B.xml new file mode 100644 index 00000000000..032a4449739 --- /dev/null +++ b/data/38/80/62/38806286906549243109D7179D3FD12B.xml @@ -0,0 +1,113 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828--9042 + + + + +Tromatobia lineatoria (Villers, 1789) + + + + +Ichneumon lineatorius +Villers, 1789 + + +oculatoria +misident. ( +Horstmann 2001a +) + + +tipulatoria +(Thunberg, 1824, +Ichneumon +) + + +balanini +(Rudow, 1883, +Ephialtes +) + + +multipicta +(Kiss, 1924, +Pimpla +) + + +sanguinolenta +(Kiss, 1924, +Pimpla +) + + +rufiventris +Hellen +, 1949 + + +amoena +(Haupt, 1954, +Pimpla +) preocc. + + +orbitalis +(Haupt, 1954, +Pimpla +) preocc. + + + +Distribution +England, Scotland, Wales, Ireland, Isle of Man + + +Notes + +Although the name oculatoria (Fabricius, 1798, +Ichneumon +) has usually been used for this species (e.g. +Fitton et al. 1988 +), the type of oculatoria is actually a species of +Lissonota +( +Horstmann 2001a +) so this species has to take the name lineatoria. + + + + \ No newline at end of file diff --git a/data/38/81/2C/38812CB4A8FB666961B344CFEFFAEE59.xml b/data/38/81/2C/38812CB4A8FB666961B344CFEFFAEE59.xml new file mode 100644 index 00000000000..51c32be16b6 --- /dev/null +++ b/data/38/81/2C/38812CB4A8FB666961B344CFEFFAEE59.xml @@ -0,0 +1,129 @@ + + + +Biting the bullet: revisionary notes on the Oraseminae of the Old World (Hymenoptera, Chalcidoidea, Eucharitidae) + + + +Author + +Burks, Roger A. +Department of Entomology, University of California, Riverside, CA 92521 + + + +Author + +Heraty, John M. +Department of Entomology, University of California, Riverside, CA 92521 +john.heraty@ucr.edu + + + +Author + +Mottern, Jason +Department of Entomology, University of California, Riverside, CA 92521 & USDA Systematic Entomology Laboratory, Washington, DC 20013 - 7012 + + + +Author + +Dominguez, Chrysalyn +Department of Entomology, University of California, Riverside, CA 92521 + + + +Author + +Heacox, Scott +Department of Entomology, University of California, Riverside, CA 92521 + +text + + +Journal of Hymenoptera Research + + +2017 + +2017-04-28 + + +55 + + +139 +188 + + + + +http://dx.doi.org/10.3897/jhr.55.11482 + +journal article +http://dx.doi.org/10.3897/jhr.55.11482 +1314-2607-55-139 +0E1B0A14F8714CD89F2910B255677621 +FFF5667EAD5E7A6FFFEC2B6CFFB7D800 +575140 + + + + +Matantas Heraty & Burks +gen. n. + + + +Type species. + + +Orasema koghisiana + +Heraty, 1994: 71-72, figs 107-108, 110, 189-190, 211-212, 219, 236, 247. + + + + +Etymology +. + +Named after one of the New Caledonia collecting localities, Matanta; gender feminine. + + +Discussion. + +Defined by +Heraty (1994 +: 71) as the + +Orasema koghisiana + +-group. No genetic sequence data are available for the group. + +Matantas koghisiana + +(Heraty) comb. n. is the only species described for the genus. + + + +Diagnosis. + +Separated from + +Orasema + +by the combination of smooth lateral areas on the propodeal disc in combination with a rugose-areolate or reticulate median channel, smooth face, and labrum with 6-8 digits. Distinguished from other Old World genera by the head subtriangular in frontal view; face smooth and relatively flattened, scrobal depression evenly impressed and lacking parallel channels or dorsal foveae; dorsal occipital margin abrupt and rounded, at most with a weak dorsal carina; funicle 7-segmented; labrum with 6-8 digits; mesonotum appearing bare, at most with minute setae; mesoscutal lateral lobes and frenum smooth; transscutal articulation complete and relatively straight; propodeal disc smooth with a broad sculptured median channel; prepectus foveate and tightly articulated with pronotum ventrally; fore wing with basal area and specular area bare, wing disc setae relatively long and dense; postmarginal vein much longer than stigmal vein and reaching about half distance to wing apex; petiole base truncate with strong basal flange; antecostal sulcus present and smooth; first valvula of ovipositor with 3 or 4 lateral teeth. Male scape lacking ventral pores. + + + +Host association. +Unknown. + + +Distribution. +One species described. New Caledonia (another undescribed species from Vanuatu, BPBM: UCRCENT00422296). + + + \ No newline at end of file diff --git a/data/38/81/D3/3881D3698C89AE712687C02BECCFFDFB.xml b/data/38/81/D3/3881D3698C89AE712687C02BECCFFDFB.xml new file mode 100644 index 00000000000..44d60160794 --- /dev/null +++ b/data/38/81/D3/3881D3698C89AE712687C02BECCFFDFB.xml @@ -0,0 +1,171 @@ + + + +A conspectus on the Canacidae (Diptera) of Brazil + + + +Author + +Mathis, Wayne N. + + + +Author + +Marinoni, Luciane + +text + + +ZooKeys + + +2012 + +162 + + +59 +92 + + + + +http://dx.doi.org/10.3897/zookeys.162.2370 + +journal article +http://dx.doi.org/10.3897/zookeys.162.2370 +1313-2970-162-59 + + + + +Dasyrhicnoessa insularis (Aldrich) +Figs 12-14 + + + + +Tethina insularis +Aldrich 1931: 395 [(United States) Wake Island; HT ♀, USNM (41629)]. + + +Rhicnoessa insularis +. +Hendel 1934 +: 44 [key], 48 [generic combination, citation]. + + +Dasyrhicnoessa insularis +. +Hardy and Delfinado 1980 +: 371-373 [generic combination, citation, figs. of head, wing, ♂ and ♀ terminalia, Oahu, Maui, Hawaii, Frigate Shoal, Pearl and Hermes Reef, Canton Island, and Palmyra Island]. +Mathis and Munari 1996 +: 12 [world catalog]. +Munari and Mathis 2010 +: 44-45 [world catalog]. + + +Tethina lasiophthalma +Malloch 1933 +: 17 [Marquesas. Hivaoa: Tahauku; HT ♂, BPBM]. +Munari 1988 +: 48 [synonymy with +Rhicnoessa ferruginea +Lamb]. + + +Dasyrhicnoessa lasiophthalma +. +Sasakawa 1974 +: 2 [generic combination]. +Steyskal and Sasakawa 1977 +: 394 [Oriental catalog]. +Foster and Mathis 1998 +: 606-608 [revision, Caribbean and Gulf of Mexico, figs. of ♂ terminalia]. +Munari and Evenhuis 2000 +: 145 [synonymy]. + + +Dasyrhicnoessa ferruginea +of authors, not Lamb 1914 [misidentification]. +Woodley and Hilburn 1994 +: 53 [citation, Bermuda]. +Munari and Evenhuis 2000 +: 145 [citation]. + + +Dasyrhicnoessa freidbergi +Munari 1994 +: 20 [Cameroon. Kribi (beach, Rt. N7); HT ♂, TAU]. +Mathis and Munari 1996 +: 12 [world catalog]. +Munari and Evenhuis 2000 +: 145 [synonymy]. + + + +Diagnosis. +This species is distinguished from congeners by the following combination of characters: Head (Fig. 12). Thorax: dark orangish brown; acrostichal setulae in 6 rows; legs yellow; forefemur bearing comb of closely set, peglike setae along distal half of anteroventral surface; midfemur bearing ctenidial comb of setae on distal half of posteroventral surface. Abdomen: Male terminalia (Figs 13-14): length of anterior surstylar-like lobe equal to or slightly shorter than surstylus; anterior surstylar-like lobe somewhat kidney shaped; surstylus bearing normal to slightly developed setae, none thickly developed. + + +Figures 12-14. +Dasyrhicnoessa insularis +12 head, lateral view 13 epandrium, surstylus and anterior surstylarlike lobe, lateral view 14 anterior surstylarlike lobe, posterior view. + + + + +Specimens examined from Brazil. + +PARANA +. Antonina ( +25°28.4'S +, +48°40.9'W +; beach/mangal), 3 +Feb- +9 Apr 2010, D. and W. N. Mathis (16♂; DZUP, USNM); Matinhos (N.; +25°46.4'S +, +48°30.8'W +; 1 m; beach/estuary), 9 Apr 2010, D. and W. N. Mathis (3♂; DZUP, USNM); +Paranagua +(Rio +Itibere +; +25°31.4'S +, +48°30.3'W +; 3 m), 23 Jan 2010, D. and W. N. Mathis (5♂, 1♀; DZUP, USNM). + + + +SAO + +PAULO. Ubatuba, Praia do Estaleiro ( +23°20.5'S +, +44°53'W +; beach), 30 Mar 2010, D. and W. N. Mathis (1♂; USNM). + + + +Distribution. + +Afrotropical: Cameroon, Madagascar, Nigeria. Australasian/Oceanian: American Samoa (Tutuila), Australia (Queensland), Bismark (Dyaul), Canton Island, Caroline Islands (Ponhpei, Chuuk, Yap, Palau), Fiji Islands (Ovalau, Suva, Viti Levu),?French Polynesia (Society Islands: Moorea), Hawaii (French Frigate Shoals, Hawaii, Hilo, Lisiansky, Maui, Midway Atoll, Molokai, Oahu, Pearl and Hermes Reef), Kiribati (Butaritari, Makin, Eita, Tarawa, Abemama), Line Islands (Christmas), Mariana Islands (Saipan, Tinian), Marquesas (Hivaoa, Nuku Hiva), Marshall Islands (Majuro, Japtan, Parry, Lib, Jibu, Jaluit, Namorik), Hebrides (Erromanga), Palmyra Island, Pitcairn Island, Rapa Island, Society Islands (Bora Bora), Wake Island. Nearctic: Bermuda, United States (Florida). Neotropical: Bahamas (South Bimini), Belize, Brazil ( +Ceara +, +Parana +, +Sao +Paulo), Mexico (Tabasco), West Indies (Cuba, Dominica, St. Kitts, St. Lucia, St. Vincent). + + + +Remarks. +This species was known previously only from the Indo-Pacific area, and its occurrence in the Caribbean, Gulf of Mexico, Bermuda, and now in Brazil represents a significant range extension. + + + \ No newline at end of file diff --git a/data/38/82/3B/38823B16F877D8462EF5D8D357163C8A.xml b/data/38/82/3B/38823B16F877D8462EF5D8D357163C8A.xml new file mode 100644 index 00000000000..96b00c7f4da --- /dev/null +++ b/data/38/82/3B/38823B16F877D8462EF5D8D357163C8A.xml @@ -0,0 +1,90 @@ + + + +Checklist of British and Irish Hymenoptera - Cynipoidea + + + +Author + +Forshage, Mattias + + + +Author + +Bowdrey, Jeremy + + + +Author + +Broad, Gavin R. + + + +Author + +Spooner, Brian M. + + + +Author + +van Veen, Frank + +text + + +Biodiversity Data Journal + + +2017 + +5 + + +8049 +8049 + + + + +http://dx.doi.org/10.3897/BDJ.5.e8049 + +journal article +http://dx.doi.org/10.3897/BDJ.5.e8049 +1314-2828--8049 + + + + +Plagiotrochus coriaceus (Mayr, 1882) -a- + + + + +Andricus coriaceus +Mayr, 1882 + + +pseudococcus +(Kieffer, 1902, +Andricus +) -a- + + + +Distribution +Wales + + +Notes + +Added by +Robbins (2007) +, based on old agamic gall only. + + + + \ No newline at end of file diff --git a/data/38/82/5D/38825D7254298970C986ADBB1A245D92.xml b/data/38/82/5D/38825D7254298970C986ADBB1A245D92.xml new file mode 100644 index 00000000000..e38f7bfa0e2 --- /dev/null +++ b/data/38/82/5D/38825D7254298970C986ADBB1A245D92.xml @@ -0,0 +1,45 @@ + + + +Liste der aus dem Somaliland von Hrn. Prof. Dr. Conr. Keller aus der Expedition des Prinzen Ruspoli im August und September 1891 zurà ¼ ckgebrachten Ameisen. + + + +Author + +Forel, A. + +text + + +Mitteilungen der Schweizerischen Entomologischen Gesellschaft + + +1892 + +8 + + +349 +354 + + + + +http://antbase.org/ants/publications/3934/3934.pdf + +journal article +3934 + + + + +4. +Polyrhachis cafrorum Forel + + + +[[ worker ]] + + + \ No newline at end of file diff --git a/data/38/82/6F/38826F237EEE54DFBD5D86AE99F25A88.xml b/data/38/82/6F/38826F237EEE54DFBD5D86AE99F25A88.xml new file mode 100644 index 00000000000..d51432fbe9b --- /dev/null +++ b/data/38/82/6F/38826F237EEE54DFBD5D86AE99F25A88.xml @@ -0,0 +1,97 @@ + + + +Rossellid glass sponges (Porifera, Hexactinellida) from New Zealand waters, with description of one new genus and six new species + + + +Author + +Reiswig, Henry M. +Biology Department, University of Victoria, Victoria, British Columbia, Canada + + + +Author + +Dohrmann, Martin +Department of Earth and Environmental Sciences, Palaeontology and Geobiology, Ludwig-Maximilians-Universitaet Muenchen, Muenchen, Germany +m.dohrmann@lrz.uni-muenchen.de + + + +Author + +Kelly, Michelle +Coasts and Oceans National Centre, National Institute of Water and Atmospheric Research, Auckland, New Zealand + + + +Author + +Mills, Sadie +NIWA Invertebrate Collection, National Institute of Water and Atmospheric Research, Wellington, New Zealand + + + +Author + +Schupp, Peter J. +ICBM Terramare, University of Oldenburg, Wilhelmshaven, Germany & Helmholtz Institute for Functional Marine Biodiversity at the University of Oldenburg (HIFMB), Oldenburg, Germany + + + +Author + +Woerheide, Gert +https://orcid.org/0000-0002-6380-7421 +Department of Earth and Environmental Sciences, Palaeontology and Geobiology, Ludwig-Maximilians-Universitaet Muenchen, Muenchen, Germany & SNSB - Bayerische Staatssammlung fuer Palaeontologie und Geologie, Muenchen, Germany & GeoBio-Center, Ludwig-Maximilians-Universitaet, Muenchen, Germany + +text + + +ZooKeys + + +2021 + +2021-09-17 + + +1060 + + +33 +84 + + + + +http://dx.doi.org/10.3897/zookeys.1060.63307 + +journal article +http://dx.doi.org/10.3897/zookeys.1060.63307 +1313-2970-1060-33 +9CF1AD759AD34890A7B359BEDA505C0D +60F647D3A76F5244AB88271A5808D0BF + + + + +Rossellinae Schulze, 1885 + + + +Diagnosis. +As for family. + + +Remarks. + +This subfamily is clearly not monophyletic ( +Dohrmann et al. 2017 +) and retained here for historical reasons only. + + + + \ No newline at end of file diff --git a/data/38/82/C6/3882C6C6C9B353F8983CDF6AD474FC7B.xml b/data/38/82/C6/3882C6C6C9B353F8983CDF6AD474FC7B.xml new file mode 100644 index 00000000000..a7623dcc3fa --- /dev/null +++ b/data/38/82/C6/3882C6C6C9B353F8983CDF6AD474FC7B.xml @@ -0,0 +1,194 @@ + + + +Comparative morphology and key to Amydetinae genera, with description of three new firefly species (Coleoptera, Lampyridae) + + + +Author + +Campello, Lucas +Programa de Pos-graduacao em Biodiversidade e Biologia Evolutiva-Laboratorio de Entomologia, Departamento de Zoologia, Instituto de Biologia, Universidade Federal do Rio de Janeiro, A 1 - 107, Bloco A, Av. Carlos Chagas Filho, 373, Cidade Universitaria, Ilha do Fundao, Rio de Janeiro, RJ, Brazil +lucas.campellog@gmail.com + + + +Author + +Vaz, Stephanie +https://orcid.org/0000-0002-2616-640X +Programa de Pos-graduacao em Biodiversidade e Biologia Evolutiva-Laboratorio de Entomologia, Departamento de Zoologia, Instituto de Biologia, Universidade Federal do Rio de Janeiro, A 1 - 107, Bloco A, Av. Carlos Chagas Filho, 373, Cidade Universitaria, Ilha do Fundao, Rio de Janeiro, RJ, Brazil + + + +Author + +Mermudes, Jose R. M. +https://orcid.org/0000-0003-2030-7483 +Programa de Pos-graduacao em Biodiversidade e Biologia Evolutiva-Laboratorio de Entomologia, Departamento de Zoologia, Instituto de Biologia, Universidade Federal do Rio de Janeiro, A 1 - 107, Bloco A, Av. Carlos Chagas Filho, 373, Cidade Universitaria, Ilha do Fundao, Rio de Janeiro, RJ, Brazil + + + +Author + +Ferreira, Andre L. D. +Programa de Pos-graduacao em Biodiversidade e Biologia Evolutiva-Laboratorio de Entomologia, Departamento de Zoologia, Instituto de Biologia, Universidade Federal do Rio de Janeiro, A 1 - 107, Bloco A, Av. Carlos Chagas Filho, 373, Cidade Universitaria, Ilha do Fundao, Rio de Janeiro, RJ, Brazil + + + +Author + +Silveira, Luiz F. L. +Laboratorio de Entomologia, Departamento de Zoologia, Instituto de Biologia, Universidade Federal do Rio de Janeiro, A 1 - 107, Bloco A, Av. Carlos Chagas Filho, 373, Cidade Universitaria, Ilha do Fundao, Rio de Janeiro, RJ, Brazil + +text + + +ZooKeys + + +2022 + +2022-07-27 + + +1114 + + +131 +166 + + + + +http://dx.doi.org/10.3897/zookeys.1114.77692 + +journal article +http://dx.doi.org/10.3897/zookeys.1114.77692 +1313-2970-1114-131 +D865EE0366174BA18064BBEE3AC72758 +9864F9CE80F25184A1D17838955E5ACE + + + + +Memoan fruhstorferi comb. nov. (Pic, 1942) + + + + +Photinus fruhstorferi +Pic, 1942: 16; +McDermott 1966 +: 39 + + +Memoan ciceroi +Silveira & Mermudes, 2013: 80 syn. nov. + + + +Remarks. + +After studying Maurice +Pic's +collection at the MNHN, we found that the holotype + +P. fruhstorferi + +of examined had all the diagnostic traits of + +Me. ciceroi + +(e.g., antenna with 10 antennomeres, apical antennomere subdivided, labial palp with one palpomere; +Silveira and Mermudes 2013 +). Therefore, we propose that + +Me. ciceroi + +is a subjective junior synonym of + +P. fruhstorferi + +Pic, 1942. + + +Pic (1942 +: 16) described + +P. fruhstorferi + +as follows: " +angustatus et elongatus +, +testaceus. Long. 6 m +, + +Bresil + +, - + +Character par sa coloration claire jointe +a +sa forme +elancee + +". The current definition of + +Photinus + +is controversial, as pointed out by several firefly specialists (e.g., +McDermott 1964 +), and needs taxonomic revision. In fact, + +P. fruhstorferi + +does not have characters normally found in + +Photinus + +, such as simple antennae shorter than 1/2 body length, pronotum with sides white and laterally expanded, abdominal tergites rounded, and phallobase relatively long ( +McDermott 1964 +). Therefore, we transfer + +P. fruhstorferi + +to + +Memoan + +, generating + +Me. fruhstorferi + +(Pic, 1942) comb. nov. and synonymize it with + +Me. ciceroi + +, syn. nov., over which it has priority. + + + +Material examined. + + + +Holotype + +: Bearing the label: + +" +Espirito Santo + +. +Brasil +. ex coll Fruhstorfer." [aged green label, typewritten]; +"TYPE" +[aged red label, typewritten]; "R Fruhstorferi" [aged white label, handwritten] (MNHN; Suppl. material 1: +Fig. S +1). + + + + + \ No newline at end of file diff --git a/data/38/84/75/3884757AC9459A05B34FF508C8D1CC3E.xml b/data/38/84/75/3884757AC9459A05B34FF508C8D1CC3E.xml new file mode 100644 index 00000000000..f59b9e6b2bd --- /dev/null +++ b/data/38/84/75/3884757AC9459A05B34FF508C8D1CC3E.xml @@ -0,0 +1,55 @@ + + + +Les formicides de l'Empire des Indes et de Ceylan. Part IV. Adjonction aux genres Camponotus, Mayr., et Polyrhachis, Shuck. + + + +Author + +Forel, A. + +text + + +Journal of the Bombay Natural History Society + + +1894 + +8 + + +396 +420 + + + + +http://antbase.org/ants/publications/3951/3951.pdf + +journal article +3951 +CA30D2B4-6420-48F9-AB0F-ED616E907611 + + + + +2. +Pl. lothneyi +, +nov. spec. + + + +Barrackporo (Rothney); Belgaum (Wroughton); Orissa (Taylor). + + +[[ queen ]] Major (voir tableau). Mandibules lisses, luisantes, ponctuees armees de 5 dents. Epistome sans carene distincte, convexe. Aire frontale, sillon frontal et ocelles distincts. Tete au moins aussi large que longue,; \ cotes convexes, assez retrecie devant. Les deux stigmates post-mesonotaux proeminent doralemsent au fond de la large et profonde echancrure neso-metanotale. Metanotum fortement elargi d'avant en arriere. Sa face basale, plutot plus longue que la face declive, passe a cette derniere par une ligne transversale droite; c'est la quo le metanotum est le plus large. D'avant en arriere, les deux faces du metanotum passent de l'une a l'antre par une courbe tres arrondie. Ecaille epaisse, amincie et attenuee au sommet. Les scapes depassent sensiblement l'occiput. +Tete et pronotum abondamment ponctues, mediocrement luisants. Mesonotum, metanotum et ecaille lisses et tres luisants, surtout le metanotum. Abdomen faiblement chagrine, plus ou moins luisant. +Pilosite dressee brunatre, courte, assez grossiere, eparse sur le corps, un peu plus abondante sur l'abdomen, nulle ou presque mille sur les scapes et les tibias. Pubescence jaunatre, assez abondante sur l'abdomen, les scapes et les tibias ou elle forme un leger duvet qui cache en partie la sculpture, mediocre sur la tete, eparse ailleurs, nulle au milieu du metanotum. +D'un noir un peu brunatre. Mandibules, scapes, base des funicules et tarses rougeatres. Le reste des pattes et des funicules, les hanches, le metasternum d'un brun plus ou moins rougeatre ou noiratre. +[[ worker ]] minor. Tete ovale, un peu plus longue que large, presque aussi etroite derriere que devant. Ocelles, sillon frontal et aire frontale peu distincts. Sculpture et pubescence beaucoup plus faibles que chez la [[ worker ]] major; tres luisante; pubescence tres eparse; tete a peine ponctuee. Les parties rougeatres chez la [[ worker ]] major sont jaunatres ou d'un jaune rougeatre chez la minor, Du reste comme la [[ worker ]] major, mais plus grele. + + + \ No newline at end of file diff --git a/data/38/84/E2/3884E28F65AC57199CD99EF5F189E17E.xml b/data/38/84/E2/3884E28F65AC57199CD99EF5F189E17E.xml new file mode 100644 index 00000000000..ce9c38b6bec --- /dev/null +++ b/data/38/84/E2/3884E28F65AC57199CD99EF5F189E17E.xml @@ -0,0 +1,116 @@ + + + +Monograph of Ceratozamia (Zamiaceae, Cycadales): an endangered genus + + + +Author + +Martinez-Dominguez, Lili +https://orcid.org/0000-0003-1158-1501 +Posgrado en Ciencias Biologicas, Instituto de Biologia, Universidad Nacional Autonoma de Mexico, 3 er. Circuito Exterior, Ciudad Universitaria, 04510, Coyoacan, CDMX, Mexico +lilimartinezd@gmail.com + + + +Author + +Nicolalde-Morejon, Fernando +https://orcid.org/0000-0003-1423-7474 +Laboratorio de Teoria Evolutiva e Historia de la Ciencia, Instituto de Biologia, Universidad Nacional Autonoma de Mexico, 3 er. Circuito Exterior, Ciudad Universitaria, 04510, Coyoacan, CDMX. Mexico + + + +Author + +Vergara-Silva, Francisco +https://orcid.org/0000-0001-5024-268X +Posgrado en Ciencias Biologicas, Instituto de Biologia, Universidad Nacional Autonoma de Mexico, 3 er. Circuito Exterior, Ciudad Universitaria, 04510, Coyoacan, CDMX, Mexico + + + +Author + +Stevenson, Dennis Wm. +https://orcid.org/0000-0002-2986-7076 +Laboratorio de Taxonomia Integrativa, Instituto de Investigaciones Biologicas, Universidad Veracruzana, Xalapa, 91190, Veracruz. Mexico +dws@nybg.org + +text + + +PhytoKeys + + +2022 + +2022-09-21 + + +208 + + +1 +102 + + + + +http://dx.doi.org/10.3897/phytokeys.208.80382 + +journal article +http://dx.doi.org/10.3897/phytokeys.208.80382 +1314-2003-208-1 +F47A23EA345757E29C2800F6D51CEE05 + + + + +Ceratozamia Brongn., Ann. Sci. Nat., Bot. ser. 3, 5: 7, t. 1. 1846. + + + +Type species. + + +Ceratozamia mexicana + +Brongn. + + + +Description. + +Stem +10-250 cm long, 8-40 cm in diameter, epigeous or semi-hypogeous, erect or decumbent. +Cataphylls +persistent, triangular to narrowly triangular, reddish brown, tomentose to densely tomentose at emergence, partially tomentose at maturity, apex acuminate. +Leaves +stipulate, ascending to descending, light green or reddish brown at emergence with whitish gray or brown trichomes, generally glabrous at maturity; stipulate 2-6 cm long, linear, tomentose at maturity. +Petiole +straight or twisted, sometimes brown in mature leaves, without prickles or heavily to lightly armed with prickles; prickles can be bifurcate. +Rachis +straight or twisted, without prickles or armed with prickles up to half the length of the leaves. +Leaflets +articulate, sessile, membranaceous to coriaceous, linear to obovate, opposite to subopposite or clustered, not imbricate, generally acuminate at apex, attenuate at base, margins entire; articulations green to brown. +Pollen strobili +1-2, with sterile tip, erect, cylindrical, green to cream with blackish to reddish brown trichomes at maturity; pollen sporangiophores deltoid to cuneate, basally stalked, distal face bicornate, fertile abaxial surface with 24-280 sporangia in clusters of (2)3(4-5), dehiscent by longitudinal slit; peduncle pubescent to tomentose. +Ovulate strobili +usually solitary, globose to cylindrical; green with pale pink to blackish trichomes at maturity, acute to apiculate apex; ovulate sporangiophores peltate with a narrow basal stalk and transversely hexagonal tips, bicornate at distal end; peduncle pubescent to tomentose, erect to pendulous. +Seeds +(ovules) 2 per megasporophyll projecting inward toward the strobilus axis, spherical, sarcotesta pink to yellowish when immature, light brown at maturity, sclerotesta smooth with several furrows longitudinal from micropylar end. + + + +Distribution and habitats. + +The 36 species of + +Ceratozamia + +are only found from Mexico to Central America, usually in montane habitats on limestone soils at elevations from 19 to 2,000 m. Most of the species are narrowly endemic, and all are on CITES Appendix I. + + + + \ No newline at end of file diff --git a/data/38/85/18/388518BED74A545DBEFB0F788442FE8C.xml b/data/38/85/18/388518BED74A545DBEFB0F788442FE8C.xml new file mode 100644 index 00000000000..371fdcd82e5 --- /dev/null +++ b/data/38/85/18/388518BED74A545DBEFB0F788442FE8C.xml @@ -0,0 +1,180 @@ + + + +Checklist of the suborder Terebrantia (Thysanoptera): generic diversity and species composition in Xishuangbanna, Yunnan Province, China + + + +Author + +Elie, Ntirenganya +https://orcid.org/0000-0002-4603-5693 +Plant Protection College, Yunnan Agricultural University, Kunming, 650201, China & Rwandan Association of Ecologists (ARECO Rwanda), Kigali, Rwanda +elientirenganya@gmail.com + + + +Author + +Yajin, Li +Agronomy and Biotechnology College, Yunnan Agricultural University, Kunming, 650201, China + + + +Author + +Yanlan, Xie +Biotechnology and Engineering College, West Yunnan University, Lincang, 677000, China + + + +Author + +Yanli, Zhou +The Germplasm Bank of Wild Species, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, 650201, China + + + +Author + +Hongrui, Zhang +https://orcid.org/0000-0002-0089-1099 +Plant Protection College, Yunnan Agricultural University, Kunming, 650201, China +hongruizh@126.com + +text + + +Biodiversity Data Journal + + +2021 + +2021-11-24 + + +9 + + +72670 +72670 + + + + +http://dx.doi.org/10.3897/BDJ.9.e72670 + +journal article +http://dx.doi.org/10.3897/BDJ.9.e72670 +1314-2828-9-e72670 +705F74B63C8850A08D6DBA243535218D + + + + +Dendrothrips strasseni Bhatti, 1971 + + + +Materials + + +Type status: + +Other material +. +Occurrence: +recordedBy: +S.S.Q +; individualID: +2009-III-15 +; individualCount: +9 +; sex: +females +; lifeStage: +adults +; occurrenceID: YAU5082020 +Tt +30; + +Taxon +: + +scientificNameAuthorship: +Dendrothrips +strasseni +Bhatti +; + +Location +: + +country: +China +; stateProvince: +Yunnan +; municipality: +Xishuangbanna +; locality: + +Jinghong +( +Nabanhe Protected Area +) + +; decimalLatitude: +21.915456 +; decimalLongitude: +101.275664 +; + +Identification +: + +identifiedBy: + +Li Yajin + +; dateIdentified: 2018; identificationReferences: ( +ThripsWiki +2020); + +Event +: + +samplingProtocol: +sweeping and shaking +; eventDate: +03-15-09 +; + +Record Level +: + +collectionID: thrips; institutionCode: YAU5082020; collectionCode: terebrantia; basisOfRecord: preserved specimen + + + + + +Ecological interactions + + +Feeds on + +leaves and collected from + +Populus tremula + +( +Salicaceae +). + + + +Distribution +Described from India and recorded from China (Xishuangbanna). + + + \ No newline at end of file diff --git a/data/38/85/53/3885538A007F58B588D093FDC1E67FFD.xml b/data/38/85/53/3885538A007F58B588D093FDC1E67FFD.xml new file mode 100644 index 00000000000..e3b449591e9 --- /dev/null +++ b/data/38/85/53/3885538A007F58B588D093FDC1E67FFD.xml @@ -0,0 +1,554 @@ + + + +Taxonomic study of the Oriental genus Catullioides Bierman, 1910 (Hemiptera, Fulgoromorpha, Tropiduchidae), with description of a new species from China + + + +Author + +Zhu, Hao-Yu +Institute of Insect Resources and Biodiversity, School of Life Sciences, Chemistry & Chemical Engineering, Jiangsu Second Normal University, Nanjing, China + + + +Author + +Yu, Fang +Institute of Insect Resources and Biodiversity, School of Life Sciences, Chemistry & Chemical Engineering, Jiangsu Second Normal University, Nanjing, China + + + +Author + +Xu, Si-Yuan +Institute of Insect Resources and Biodiversity, School of Life Sciences, Chemistry & Chemical Engineering, Jiangsu Second Normal University, Nanjing, China + + + +Author + +Ma, Fang-Zhou +Nanjing Institute of Environmental Sciences, Ministry of Ecology and Environment, Nanjing, China + + + +Author + +Wang, Rong-Rong +Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, China +wangrr_2008@163.com + + + +Author + +Song, Zhi-Shun +https://orcid.org/0000-0002-5449-4646 +Institute of Insect Resources and Biodiversity, School of Life Sciences, Chemistry & Chemical Engineering, Jiangsu Second Normal University, Nanjing, China +songzs@jssnu.edu.cn + +text + + +ZooKeys + + +2021 + +2021-05-17 + + +1037 + + +119 +136 + + + + +http://dx.doi.org/10.3897/zookeys.1037.65481 + +journal article +http://dx.doi.org/10.3897/zookeys.1037.65481 +1313-2970-1037-119 +10E8FE8D686F4C5E9445BCC7FCFA5E95 +4925625650725788BAD3F2AFACDFA912 + + + + +Catullioides rubrolineata Bierman, 1910 +Figures 1 +, 2 +, 3 +, 4 +, 5 + + + + +Catullioides rubrolineata +Bierman, 1910: 22, pl. 1, fig. 9a-d. + + +Barunoides albosignata +(Distant): +Melichar (1914 +: 140) [error]. + + +Catullioides albosignatus +(Distant): +Yang et al. (1989 +: 74, fig. 3); +Hayashi (1995 +: 65, fig. 1) [error]. + + + +Redescription. +Body length from apex of head to tip of forewings: ♂ 8.4-9.5 mm, ♀ 9.4-10.3 mm; head length from apex of cephalic process to base of eyes: ♂ 0.7-0.8 mm, ♀ 0.8-0.9 mm; head width including eyes: ♂ 1.3-1.4 mm, ♀ 1.4-1.5 mm; forewing length: ♂ 7.0-7.7 mm, ♀ 8.1-8.6 mm. + + +Coloration +. + +Sexual dimorphism in general color (Fig. +1 +). Females distinctly paler on body than males (Fig. +2 +). General color pale green and red on head and thorax, and dark brown on body. Head excluding eyes, pronotum and mesonotum mostly pale green to yellowish green, broad stripes along median carinae of vertex, frons, clypeus, pronotum and mesonotum, lateral margins of frons, lateral areas of pronotum and mesonotum behind eyes red, clypeus and apical margins of paranotal lobes dark brown to black. Compound eyes red to fuscous with posterior margin pale green, ocelli purplish red. Forewings, in males (Fig. +3D +), with central area of basal two-thirds and apical third dark brown to black, clavus, apices of costal area, postcostal cell, veins C1 and C2 yellowish green; in females (Fig. +3F +), much paler than in males, mostly yellowish green, central area of basal two-thirds and Medial area dark brown to black. Thorax and abdomen mostly black in males (Fig. +2C +); in females (Fig. +2D +), much paler than in males, mostly yellowish brown. + + + +Figure 1. +Habitus of + +Catullioides rubrolineata + +Bierman +A +male +B +female. Photographed by Z-S Song. + + + + +Figure 2. + +Catullioides rubrolineata + +Bierman +A +male, dorsal view +B +female, dorsal view +C +male, lateral view +D +female, lateral view. Scale bars: 2 mm. + + + + +Structure +. + +Vertex (Fig. +3A +) wider than length, with ratio of length at midline to width between eyes 0.5:1. Frons with ratio of length at midline to maximum width 1.6:1 (Fig. +3C +). Forewings (Fig. +3D, F +) almost flat, ratio of length to width about 2.9-3.2:1. Hindwings (Fig. +3E, G +) with ratio of length to width about 1.9-2.0:1. + + + +Figure 3. + +Catullioides rubrolineata + +Bierman +A +head, pronotum and mesonotum, dorsal view +B +head and pronotum, lateral view +C +head and pronotum, ventral view +D +forewing of male +E +hindwing of male +F +forewing of female +G +hindwing of female. Abbreviations: nl, nodal line. Scale bars: 1 mm. + + + + +Male genitalia +. + +Pygofer, in lateral view (Figs +4A +, +4B +), with posterior margin slightly sinuate, more or less convex medially, anterior margin produced in a pair of broad and large sclerotised processes ventrolaterally; in ventral view (Fig. +4D +), far longer than in dorsal view (Fig. +4C +), with ratio of ventral to dorsal width about 4.5:1. Gonostyles (Fig. +4A, B, D +) elongate, in ventral view (Fig. +4D +), inner area along ventrolateral carina less sclerotised and filmy, dorso-basal process directed dorsolaterad; in lateral view (Fig. +4A, B +), ventrolateral carina strongly ridged from base to apex. Aedeagus (Fig. +4E-H +) large and elongate, as long as gonostyles; in right lateral view (Fig. +4F +), right apical process directed dorsad and curved laterocaudad; in left lateral view (Fig. +4G +), left process large and broad, base narrow and twisted, remaining cultrate, directed laterocaudad. Segment X (Fig. +4C +) slender and elongate, anal style relatively small, not reaching to apex. + + + +Figure 4. + +Catullioides rubrolineata + +Bierman +A +male pygofer, gonostyles, and segment X, left lateral view +B +male pygofer, gonostyles, and segment X, right lateral view +C +male segment X and pygofer, dorsal view +D +male pygofer and gonostyles, ventral view +E +aedeagus, dorsal view +F +aedeagus, left lateral view +G +aedeagus, right lateral view +H +aedeagus, ventral view. Abbreviations: as, anal style; bpg, basal process of gonostyle; dmp, dorsal margin of pygofer in profile; dp, dorsal process of phallotheca; gs, gonostyle; hpg, hook-like process of gonostyle; lp, left process of phallotheca; ml, membranous lobe of phallotheca; pen, periandrium; pg, pygofer; pmpg, posterior margin of pygofer in profile; rap, right apical process of phallotheca; rbp, right basal process of phallotheca; sp, sclerotised processes of pygofer; sx, segment X; vc, ventrolateral carina of gonostyle; vmp, ventral margin of pygofer in profile. Scale bars: 0.5 mm. + + + +Female genitalia +(Figs +5A-I +) as in generic description. + + + +Figure 5. + +Catullioides rubrolineata + +Bierman +A +female terminalia, dorsal view +B +female terminalia, lateral view +C +female terminalia, ventral view +D +female segment X, dorsal view +E +gonapophyses VIII, lateral view +F +gonapophyses VIII, ventral view +G +gonapophyses VIII and IX, ventral view +H +gonapophyses IX, ventral view +I +gonoplacs, lateral view. Abbreviations: ACL, anterior connective lamina of gonapophysis VIII; as, anal style; Gp, gonoplacs; PCL, posterior connective lamina of gonapophysis IX; sx, segment X. Scale bars: 0.5 mm ( +A-C, G, I +); 0.2 mm ( +D-F, H +). + + + + +Material examined. + + + +China + +: +7♂♂ +, +6♀♀ +, +Zhejiang +, +Taishun +, +Beikengdi +( +27°28'30"N +, +119°54'28"E +), + +469 m + +, +light trap +, +28.viii.2020 +, +F.Z. Ma +, +S.Y. Xu +& H.Y. +Zhu + +; +2♂♂ +, +2♀♀ +, same collecting locality and time, F.Z. Ma, S.Y. Xu & H.Y. Zhu (all in JSSNU); + +1♀ +, +Hainan +, +Shuiman +, + +640 m + +, +29.v.1960 +, +S.F. Li + +; + +8♂♂ +, +3♀♀ +, +Fujian +, +Jiangle +, +Longqi Moutain +, + +200 m + +, +10.viii.1991 +, +S.M. Song + +; + +1♀ +, +Fujian +, +Jiangle +, +Longqishan +, + +500 m + +, +13.viii.1991 +, +X.C. Zhang + +; + +8♂♂ +, +2♀♀ +, +Yunnan +, +Hekou +, + +80 m + +, +light trap +, +7.vi.1956 +, +K.R. Huang + +; + +1♂ +, +Yunnan +, +Xishuangbanna +, +Mengla +, + +620-650 m + +, +9.vi.1959 +, +S.F. Li + +; + +1♀ +, +Yunnan +, +Jinghong +, +Damenglong +, +30.ix.1979 +, +J.X. Cui +(all in IZCAS) + +. + + +Vietnam + +: +1♂ +, +Kontum +N of Pleiku +, + +550 m + +, +13.v.1960 +, +L.W. Quate + +. + + +Laos + +: +1♀ +, +Borikhane Prov. +Paksane, +20.xii.1965 +, native collector + +; + +1♂ +, +Vientiane Prov. +Tha Ngone +, +30.xi.1965 +, native collector + +. + + +Malaysia + +: +1♀ +, +Borneo +, +Sarawak +Sadong +, +Kampong Tapuh +, + +300-450 m + +, +10.vii.1958 +, +T.C. Maa +(all in BPBM) + +. + + + +Host plant. + + +Miscanthus floridulus + +. + + + +Distribution. +China (Zhejiang, Hainan, Fujian, Yunan, Taiwan); Japan (Ryukyu Islands); Vietnam; Laos; Malaysia; Indonesia. + + +Remarks. + + +Catullioides rubrolineata + +is newly recorded from Vietnam and Laos. Our specimens are distinctly larger than those recorded from Taiwan, China by +Yang et al. (1989) +. Their data showed the body length of + +C. rubrolineata + +from Nantou, Taiwan as 5.27 ++/- +0.11 mm in males and 5.76 ++/- +0.33 mm in females ( +Yang et al. 1989 +). The type specimens of + +C. rubrolineata + +from Indonesia (6.5-8.0 mm) are also a little shorter than the specimens we examined ( +Bierman 1910 +). Unfortunately, we did not examine the syntypes of +Bierman (1910) +and the specimens of +Yang et al. (1989) +, and identified this species based on our critical review of the literature. + + + + \ No newline at end of file diff --git a/data/38/85/B3/3885B3A3E7C458F54193C5F41EC52AC0.xml b/data/38/85/B3/3885B3A3E7C458F54193C5F41EC52AC0.xml new file mode 100644 index 00000000000..38af96b0f27 --- /dev/null +++ b/data/38/85/B3/3885B3A3E7C458F54193C5F41EC52AC0.xml @@ -0,0 +1,93 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part S) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +806 +877 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Smyrnium integerrimum +Linnaeus + +, + +Species Plantarum +1 + +: 263. 1753 + + +. + + + +"Habitat in Virginia." RCN: 2097. + + + + +Lectotype +(Reveal in Jarvis & al. in +Taxon +55: 215. 2006): +Clayton 549 +, Herb. Linn. No. 370.7 ( +LINN +; +iso- +BM +) + +. + + + + +Current name: + + +Taenidia integerrima + +(L.) Drude + +( +Apiaceae +). + + + + \ No newline at end of file diff --git a/data/38/87/19/388719706BE1677531AF921915ADA782.xml b/data/38/87/19/388719706BE1677531AF921915ADA782.xml new file mode 100644 index 00000000000..5707655c407 --- /dev/null +++ b/data/38/87/19/388719706BE1677531AF921915ADA782.xml @@ -0,0 +1,135 @@ + + + +Order Scandentia + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +104 +109 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Anathana ellioti +(Waterhouse 1849) + + + + + + + +[Tupaia] ellioti +Waterhouse 1849 + +, +Proc. Zool. Soc. Lond., 1849: 107 + +. + + + + +Type Locality: + +India +, +Andhra Pradesh +, "hills between Cuddapah and Nellox" (= Velikanda Range). + + + + + +Vernacular Names: +Madras Treeshrew +. + + + + +Synonyms: + +Anathana pallida +Lyon 1913 + +; + +Anathana wroughtoni +Lyon 1913 + +. + + + + +Distribution: +India +south of the Ganges River. + + + + +Conservation: +CITES +– Appendix II; +IUCN +– Lower Risk (nt). + + + + +Discussion: +Museum material of + +Anathana + +is very limited. +Lyon (1913) +named + +pallida + +and + +wroughtoni + +as full species based on minor pelage differences; Corbet (in +Corbet and Hill, 1992 +) is probably correct in his assumption that these three "intergrade without definable boundaries.". + + + + \ No newline at end of file diff --git a/data/38/87/8C/38878C46A145295711A536B1D103982E.xml b/data/38/87/8C/38878C46A145295711A536B1D103982E.xml new file mode 100644 index 00000000000..8679547b113 --- /dev/null +++ b/data/38/87/8C/38878C46A145295711A536B1D103982E.xml @@ -0,0 +1,76 @@ + + + +Macrobenthic fauna from an upwelling coastal area of Peru (Warm Temperate South-eastern Pacific province - Humboldtian ecoregion) + + + +Author + +Tasso, Vicente + + + +Author + +El Haddad, Mustapha + + + +Author + +Assadi, Carolina + + + +Author + +Canales, Remy + + + +Author + +Aguirre, Luis + + + +Author + +Velez-Zuazo, Ximena + +text + + +Biodiversity Data Journal + + +2018 + +6 + + +28937 +28937 + + + + +http://dx.doi.org/10.3897/BDJ.6.e28937 + +journal article +http://dx.doi.org/10.3897/BDJ.6.e28937 +1314-2828--28937 + + + + +Caecum chilense Stuardo, 1962 + + + +Notes +Types of substrate: hard bottom. Depth / bathymetric range: 5 m. Station code: D4(5). + + + \ No newline at end of file diff --git a/data/38/88/70/388870B1C031F9E28C4F39BD98F25B4F.xml b/data/38/88/70/388870B1C031F9E28C4F39BD98F25B4F.xml new file mode 100644 index 00000000000..c36075f9a82 --- /dev/null +++ b/data/38/88/70/388870B1C031F9E28C4F39BD98F25B4F.xml @@ -0,0 +1,66 @@ + + + +Annotated checklist of the leech species diversity in the Maloe More Strait of Lake Baikal, Russia + + + +Author + +Kaygorodova, Irina A. + +text + + +ZooKeys + + +2015 + +545 + + +37 +52 + + + + +http://dx.doi.org/10.3897/zookeys.545.6053 + +journal article +http://dx.doi.org/10.3897/zookeys.545.6053 +1313-2970-545-37 +5F786F123BD940CF838C7F31F7F3F93B +5F786F123BD940CF838C7F31F7F3F93B + + + +Taxon classification Animalia Arhynchobdellida Erpobdellidae + + + +Erpobdella sp. 2 + + + +New species records. +Lake Zama, Lake Zunduk, Codoviy Bay. + + +Morphological characteristics. +These large sized leeches are up to 90 mm in length and 4.5-5.0 mm in width. The leeches have dark green or brown dorsal pigmentation flecked with yellow. Ventral pigmentation is almost absent (Fig. 7). + + +Figure 7. +Erpobdella +sp. 2 from Codoviy Bay (Maloe More Strait, Lake Baikal). Scale bar 5 mm. + + + + +Ecological characteristics. +This non-parasitic macrophagous leech species has a restricted distribution even within the Maloe More. It was found only in lakes and bays of the most north-western coast of the strait. + + + \ No newline at end of file diff --git a/data/38/89/01/3889012E654052C79275DB1E4E042590.xml b/data/38/89/01/3889012E654052C79275DB1E4E042590.xml new file mode 100644 index 00000000000..93af392533d --- /dev/null +++ b/data/38/89/01/3889012E654052C79275DB1E4E042590.xml @@ -0,0 +1,72 @@ + + + +Revisiting the taxonomy of Dioclea and related genera (Leguminosae, Papilionoideae), with new generic circumscriptions + + + +Author + +Queiroz, Luciano Paganucci de +Programa de Pos-Graduacao em Botanica, Universidade Estadual de Feira de Santana, Av. Transnordestina s / n, Novo Horizonte, 44036 - 900, Feira de Santana, BA, Brazil +luciano.paganucci@gmail.com + + + +Author + +Snak, Cristiane +Programa de Pos-Graduacao em Botanica, Universidade Estadual de Feira de Santana, Av. Transnordestina s / n, Novo Horizonte, 44036 - 900, Feira de Santana, BA, Brazil & Departamento de Engenharia de Pesca e Ciencias Biologicas, Universidade do Estado de Santa Catarina, Rua Cel. Fernandes Martins 270, Progresso, 88790 - 000, Laguna, Santa Catarina, Brazil + +text + + +PhytoKeys + + +2020 + +164 + + +67 +114 + + + + +http://dx.doi.org/10.3897/phytokeys.164.55441 + +journal article +http://dx.doi.org/10.3897/phytokeys.164.55441 +1314-2003-164-67 +F8BB69882078557CB69041DA4DEAEA61 + + + + +4.1.22. + +Macropsychanthus lauterbachii Harms, in Schumann & Lauterb. Fl. Schutzgeb. +Suedsee +367. 1900. + + + + +Type. + +Papua New Guinea, Nurufluss, +Lauterbach s.n. +(lectotype, designated here from the syntypes: WRSL!; isolectotype: B †). + + + +4.1.22.1. +Macropsychanthus lauterbachii Harms var. lauterbachii +in Verdcourt, Kew Bull. 32(2): 455. 1978. + + + + + \ No newline at end of file diff --git a/data/38/89/DF/3889DFFE10CDE5D032D5CDA0203AAE75.xml b/data/38/89/DF/3889DFFE10CDE5D032D5CDA0203AAE75.xml new file mode 100644 index 00000000000..12123aa2857 --- /dev/null +++ b/data/38/89/DF/3889DFFE10CDE5D032D5CDA0203AAE75.xml @@ -0,0 +1,53 @@ + + + +Formicidae. + + + +Author + +Santschi, F. + +text + + +Voyage de Ch. Alluaud et R. Jeannel en Afrique Orientale (1911 - 1912). Résultats scientifiques. Hyménoptères + + +1914 + +2 + + +41 +148 + + + + +http://antbase.org/ants/publications/8111/8111.pdf + +journal article +8111 + + + + +Dorylus affinis Schuckard +. + + + +Ann. Mag. nat. Hist., vol. 5, p. 316 (1840), [[male]]. - Emery, apud P. Wytsman, Genera Insectorum, Formicidae, subfam. Dorylinae, fase. CII, p. 9 (1910). + + + +Afrique orientale anglaise: Mombasa (st. n° 3, nov. 1911), plusieurs [[worker]]; - lac Victoria-Nyanza, baie de Kavirondo, 1 [[worker]]; - Mail escarpment, entre El Burgon et Ndjoro (2.100 m., st. n° 24, dec. 1911), 3 [[worker]] et [[male]]. -La couleur sombre de ces exemplaires me fait supposer qu'ils sont peut-etre les ouvrieres de la +var. exilis +Santschi, dont le male seul est connu. + +Uganda: prov. d'Unyoro, pres Hoima (1909), 2 [[male]]; - reg. a l'est de l'Albert-Nyanza, 2 [[male]]; - Uganda central: M'Bale (1909), 3 [[male]]. + + + \ No newline at end of file diff --git a/data/38/89/FA/3889FA3CD3A5A88120F8E7C211B8FD0D.xml b/data/38/89/FA/3889FA3CD3A5A88120F8E7C211B8FD0D.xml new file mode 100644 index 00000000000..517cf6a9411 --- /dev/null +++ b/data/38/89/FA/3889FA3CD3A5A88120F8E7C211B8FD0D.xml @@ -0,0 +1,89 @@ + + + +Annotated checklist of the leech species diversity in the Maloe More Strait of Lake Baikal, Russia + + + +Author + +Kaygorodova, Irina A. + +text + + +ZooKeys + + +2015 + +545 + + +37 +52 + + + + +http://dx.doi.org/10.3897/zookeys.545.6053 + +journal article +http://dx.doi.org/10.3897/zookeys.545.6053 +1313-2970-545-37 +5F786F123BD940CF838C7F31F7F3F93B +5F786F123BD940CF838C7F31F7F3F93B + + + +Taxon classification Animalia Rhynchobdellea Piscicolidae + + + +Baicalobdella cottidarum Dogiel, 1957 + + + + +Trachelobdella torquata +(part.): +Epstein 1959 +; +Trachelobdella torquata +(part.): +Epstein 1959 +; +Trachelobdella torquata +(part.): +Kozhov 1962 +; +Trachelobdella torquata +(part.): Lukin 1963; +Baicalobdella torquata +(part.): +Lukin 1976 +. + + + +Geographic distribution. +Endemic to Lake Baikal. +Maloe More: Kurma Bay; Olkhon Gates Strait; Kharansa Bay. + + + +Ecological +characteristics. + + +This species inhabits the littoral zone of Lake Baikal (0-200 m). This species is less abundant in the Maloe More area than its sister species, +Baicalodbella torquata +. In contradistinction to +Baicalodbella torquata +, it parasitizes only Baikal cottoid fishes. +Baicalobdella cottidarum +can be found directly on a host or in a free-living state on the surface of benthic substrates. + + + + \ No newline at end of file diff --git a/data/38/8A/73/388A73FA9F25F6E062958D2C5922B79E.xml b/data/38/8A/73/388A73FA9F25F6E062958D2C5922B79E.xml new file mode 100644 index 00000000000..b7948589a94 --- /dev/null +++ b/data/38/8A/73/388A73FA9F25F6E062958D2C5922B79E.xml @@ -0,0 +1,64 @@ + + + +Checklist of British and Irish Hymenoptera - Braconidae + + + +Author + +Broad, Gavin R. + + + +Author + +Shaw, Mark R. + + + +Author + +Godfray, H. Charles J. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8151 +8151 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8151 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8151 +1314-2828--8151 + + + + +Dolichogenidea lineipes (Wesmael, 1837) + + + + +Microgaster lineipes +Wesmael, 1837 + + + +Distribution +England, Scotland, Isle of Man + + + \ No newline at end of file diff --git a/data/38/8B/85/388B854AEE04C2C1EB6D09AFC39816CD.xml b/data/38/8B/85/388B854AEE04C2C1EB6D09AFC39816CD.xml new file mode 100644 index 00000000000..52a0b132482 --- /dev/null +++ b/data/38/8B/85/388B854AEE04C2C1EB6D09AFC39816CD.xml @@ -0,0 +1,51 @@ + + + +A synoptic review of the ants of California (Hymenoptera: Formicidae). + + + +Author + +Ward, P. S. + +text + + +Zootaxa + + +2005 + +936 + + +1 +68 + + + + +http://antbase.org/ants/publications/21008/21008.pdf + +journal article +21008 + + + + + + +Aphaenogaster patruelis Forel +1886b + + + + + +E2 [endemic to California floristic province (Hickman, 1993)] + + + + + \ No newline at end of file diff --git a/data/38/8B/B3/388BB38F09C971AA82B13AEFD9AE101D.xml b/data/38/8B/B3/388BB38F09C971AA82B13AEFD9AE101D.xml new file mode 100644 index 00000000000..2c57661d3cd --- /dev/null +++ b/data/38/8B/B3/388BB38F09C971AA82B13AEFD9AE101D.xml @@ -0,0 +1,91 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part A) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +252 +342 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Anthericum serotinum +(Linnaeus) Linnaeus + +, + +Species Plantarum +, ed. 2, 1 + +: 444. 1762 + + +. + + + +"Habitat in alpibus Angliae, Helvetiae, Taureri rastadiensis, Wallaesiae." RCN: 2441. + + + +Basionym: + +Bulbocodium serotinum +L. (1753) + +. + + + +Type not designated. + + +Original material: as basionym. + + + +Current name: + + +Lloydia serotina + +(L.) Rchb. + +( +Liliaceae +). + + + + \ No newline at end of file diff --git a/data/38/8B/E5/388BE5ACB42BE7F31BBD73F1779D8077.xml b/data/38/8B/E5/388BE5ACB42BE7F31BBD73F1779D8077.xml new file mode 100644 index 00000000000..b30b2592e7f --- /dev/null +++ b/data/38/8B/E5/388BE5ACB42BE7F31BBD73F1779D8077.xml @@ -0,0 +1,144 @@ + + + +An annotated checklist of the Chilopoda and Diplopoda (Myriapoda) of the Abrau Peninsula, northwestern Caucasus, Russia + + + +Author + +Korobushkin, Daniil I. + + + +Author + +Semenyuk, Irina I. + + + +Author + +Tuf, Ivan H. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +7308 +7308 + + + + +http://dx.doi.org/10.3897/BDJ.4.e7308 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e7308 +1314-2828-4-7308 + + + + +Trachysphaera costata (Waga, 1857) + + + +Materials + + +Type status: +Other material +. Occurrence: recordedBy: +IIS; Sampling: Hand +; individualCount: +20 +; Location: country: +Russia +; stateProvince: Krasnodar; locality: +{16} +; verbatimCoordinates: +44°44'27''N +, +37°29'53'' E +; 295; Event: eventDate: +06/2011 + + +Type status: +Other material +. Occurrence: recordedBy: +IIS; Sampling: Hand +; individualCount: +12 +; Location: country: +Russia +; stateProvince: Krasnodar; locality: +{18} +; verbatimCoordinates: +44°44'02''N +, +37°29'32'' E +; 172; Event: eventDate: +06/2011 + + +Type status: +Other material +. Occurrence: recordedBy: +IIS; Sampling: Hand +; individualCount: +13 +; Location: country: +Russia +; stateProvince: Krasnodar; locality: +{19} +; verbatimCoordinates: +44°44'10''N +, +37°28'47'' E +; 149; Event: eventDate: +06/2011 + + +Type status: +Other material +. Occurrence: recordedBy: +IIS; Sampling: Hand +; individualCount: +23 +; Location: country: +Russia +; stateProvince: Krasnodar; locality: +{15} +; verbatimCoordinates: +44°45'02''N +, +37°30'05'' E +; 273; Event: eventDate: +06/2013 + + + + +Notes + +T. costata +is known from parthenogenetic populations in Central and Eastern Europe, as well as in some areas in the Caucasus, while bisexual populations are restricted to southern Romania, the Balkans, Anatolia, Israel, most of the Caucasus, and Crimea ( +Golovatch 2008 +, +Golovatch 2012 +). Quite often specimens are found in caves ( +Golovatch 2008 +). In the Abrau Peninsula, the species was collected from the upper soil and lower leaf litter layers. + + + + \ No newline at end of file diff --git a/data/38/8C/55/388C55BDCFE402018D4237BD72A19EFC.xml b/data/38/8C/55/388C55BDCFE402018D4237BD72A19EFC.xml new file mode 100644 index 00000000000..5a279a738a3 --- /dev/null +++ b/data/38/8C/55/388C55BDCFE402018D4237BD72A19EFC.xml @@ -0,0 +1,265 @@ + + + +A new species and range extensions for three other species of pebblesnails (Lithoglyphidae, Fluminicola) from the upper Klamath basin, California-Oregon + + + +Author + +Liu, Hsiu-Ping + + + +Author + +Hershler, Robert + +text + + +ZooKeys + + +2019 + +812 + + +47 +67 + + + + +http://dx.doi.org/10.3897/zookeys.812.29205 + +journal article +http://dx.doi.org/10.3897/zookeys.812.29205 +1313-2970-812-47 +940784938803416F83DB04B0BEACBD92 +940784938803416F83DB04B0BEACBD92 + + + + +Fluminicola multifarius Hershler, Liu, Frest & Johannes, 2007 +Figures 3, 9 + + + + + +Fluminicola +multifarius + +- +Hershler et al. 2007 +: 415, 417, 419, figs 7M, 24, 25 (Big Springs (source) at Big Springs City Park northwest of the city of Mount Shasta, south of Spring Hill, Siskiyou County, California ([UTM zone 10] 556400 E, 4575265 N, 1092 m). + + + +Distribution. + +Sacramento River headwater region, upper reaches of the McCloud and Rogue River drainages, +California-Oregon +( +Hershler et al. 2007 +; +Hershler et al. 2017 +). + + + +Referred material. + +CALIFORNIA. Siskiyou County: USNM 1207974, Spring on Close Butte ( +41.9884N +, +122.3229W +), USNM 1190109, Spring northwest of Copco Reservoir ( +41.9873N +, +122.3275W +), USNM 1145066, USNM 1190108, Fall Creek above Copco Road bridge ( +41.9834N +, +122.3623W +). OREGON. Jackson County: USNM 1144324, USNM 1144325, USNM 1144326, USNM 1144898, USNM 1145117, USNM 1190128, USNM 1243229, USNM 1254453, Fredenburg Spring +( +42.1669N +, +122.3268W +), USNM 1207971, Spring Creek north of Schoolhouse Meadow ( +42.0357N +, +122.3397W +), USNM 1144903, USNM 1190105, USNM 1207969, Spring brook below Schoolhouse Meadow ( +42.0288N +, +122.3374W +), USNM 1144342, USNM 1144943, USNM 1144365, USNM 1144366, USNM 1144484, USNM 1190114, Keene Creek, east of bridge on Mill Creek Road ( +42.1046N +, +122.4136W +), USNM 1144368, USNM 1144718, USNM 1144946, USNM 1190103, Rattlesnake Spring ( +42.0625N +, +122.3389W +), USNM 1190104, Shoat Spring, source ( +42.0466N +, +122.3360W +), USNM 1207968, Shoat Springs, outflow near source ( +42.0456N +, +122.3367W +), USNM 1207970, Spring channel above Schoolhouse Meadow, adjacent to cabin ruins ( +42.0327N +, +122.3379W +), USNM 1144536, USNM 1144537, USNM 1144941, USNM 1144942, USNM 1190118, Spring north of Hyatt Reservoir ( +42.2064N +, +122.4498W +), USNM 1144540, USNM 1144541, USNM 1144907, USNM 1144993, USNM 1190131, Nameless Spring, outflow ( +42.2183N +, +122.3087W +), USNM 1190129, Bluejay Spring ( +42.1810N +, +122.3368W +), USNM +1144587 +, USNM 1190115, Spring, Chinquapin Mountain ( +42.1409N +, +122.4268W +), USNM 1190116, Spring along Beaver Creek Road ( +42.1467N +, +122.4165W +), USNM 1190117, Spring, Craine Prairie ( +42.1754N +, +122.4086W +), USNM 1190111, Spring north of Soda Spring ( +42.1025N +, +122.3684W +), USNM 1190119, Spring, west side of Burnt Creek Road ( +42.1761N +, +122.4911W +), USNM 1144655, USNM 1145079, USNM 1190130, Jenny Creek Spring ( +42.2034N +, +122.3443W +). Klamath County: USNM 1469081, USNM 1469089, Wood River, south spring source ( +42.7372N +, +121.9775W +), USNM 1190138, Spring west of Klamath River ( +42.0257N +, +122.1351W +), USNM 1144392, USNM 1144951, USNM 1190127, Tiger Lily Spring ( +42.6156N +, +122.0935W +), USNM 1144393, USNM 1190092, Four Mile Spring ( +42.6331N +, +122.0778W +), USNM 1469079, Spring, Klamath Fish Hatchery ( +42.6519N +, +121.9479W +), USNM 1469083, Reservation Spring ( +42.7023N +, +121.9629W +), USNM 1469084, Spring Creek, headspring ( +42.6690N +, +121.8860W +), USNM 1144414, USNM 1144965, USNM 1190091, Short Creek, headspring ( +42.7000N +, +122.0776W +), USNM 1144416, USNM 1207975, Rainbow Springs ( +42.3239N +, +122.2040W +), USNM 1190134, Cold Creek, south of Lake of the Woods ( +42.3434N +, +122.2083W +), USNM 1144463, USNM 1190133, Spring along western edge of Buck Lake ( +42.2670N +, +122.1995W +), USNM 1190132, Johnson Creek ( +42.2401N +, +122.2399W +), USNM 1144468, USNM 1190136, Spring (northernmost), Denny Creek ( +42.3552N +, +122.0286W +), USNM 1144887, USNM 1144984, USNM 1190135, Spring (southernmost), Denny Creek ( +42.3324N +, +122.0221W +). Lake County: USNM 1190125, Spring, Holmes Meadow ( +42.1761N +, +120.8350W +), USNM 1144564, USNM 1185799, Blonde Spring ( +42.4149N +, +120.7467W +). + + + +Remarks. + +The UKL +F. multifarius +range from 2.1-5.1 mm in shell height and, as noted above, vary considerably in shell shape and appearance of the inner apertural lip between and sometimes within populations. There is also considerable variation in the number of cusps on the radular teeth; and the size and shape of the cusps and indentation of the dorsal edge of the central teeth (Fig. 9). Radula: central teeth with 2-6 lateral cusps, 1-6 basal cusps; lateral teeth with 3-7 cusps on outer side; 2-6 cusps on inner side; inner marginal teeth with 16-35 cusps; outer marginal teeth with 22-40 cusps (USNM 1144326, USNM 1144342, USNM 1144368, USNM 1144463, USNM 1144540, USNM 1144564, USNM 1144588, USNM 1144951, USNM 1145079, USNM 1207968, USNM 1207970, USNM 1207974). + + + +Figure 9. Variation in central radular teeth, UKL +F. multifarius +A, C, E USNM 1207968 B USNM 144951 D USNM 1144368 F Central teeth, USNM 1207970. Scale bar: 10 +µm +. + + + +Fifty-one (51) COI and 52 cytB haplotypes were detected in the UKL specimens of +F. multifarius +(Suppl. materials 2, 3, respectively). + + +The "Fredenburg pebblesnail" (also referred to as +Fluminicla +n. sp. 17) and "Klamath Rim pebblesnail" (also referred to as +Fluminicola +n. sp. 3), which were recognized by Frest and Johannes in their UKL contract reports (also see +Frest and Johannes 1999 +) and subsequently included in the Northwest Forest Plan as Survey and Manage species, correspond to +F. multifarius +. + + +The new records detailed herein extend the range of +F. multifarius +about 150 km eastward from the Rogue River headwaters. Populations of this species are distributed in close proximity (ca 1 km) across the divide between the Rogue River and UKL basins (springs in Sampson Creek and Burnt Creek drainages, respectively). + + + + \ No newline at end of file diff --git a/data/38/8C/9C/388C9CEAE5BB64C60E17A5A818C43DB5.xml b/data/38/8C/9C/388C9CEAE5BB64C60E17A5A818C43DB5.xml new file mode 100644 index 00000000000..42b3d180c42 --- /dev/null +++ b/data/38/8C/9C/388C9CEAE5BB64C60E17A5A818C43DB5.xml @@ -0,0 +1,75 @@ + + + +Polychaetes of Greece: an updated and annotated checklist + + + +Author + +Faulwetter, Sarah + + + +Author + +Simboura, Nomiki + + + +Author + +Katsiaras, Nikolaos + + + +Author + +Chatzigeorgiou, Giorgos + + + +Author + +Arvanitidis, Christos + +text + + +Biodiversity Data Journal + + +2017 + +5 + + +20997 +20997 + + + + +http://dx.doi.org/10.3897/BDJ.5.e20997 + +journal article +http://dx.doi.org/10.3897/BDJ.5.e20997 +1314-2828-5-20997 + + + + +Glycera lapidum Quatrefages, 1866 + + + +Notes + +O'Connor (1987) +reports at least four varieties amongst the examined material from the North-East Atlantic, although these correspond in fact to different species ( +Boeggemann +, pers. comm.). + + + + \ No newline at end of file diff --git a/data/38/8C/C2/388CC27EA9231CF395450B041EDEF76C.xml b/data/38/8C/C2/388CC27EA9231CF395450B041EDEF76C.xml new file mode 100644 index 00000000000..bbb8534014b --- /dev/null +++ b/data/38/8C/C2/388CC27EA9231CF395450B041EDEF76C.xml @@ -0,0 +1,94 @@ + + + +Revision of the ant genus Myrmoteras in the Malay Archipelago (Hymenoptera, Formicidae). + + + +Author + +Agosti, D. + +text + + +Revue Suisse de Zoologie + + +1992 + +99 + + +405 +429 + + + +journal article +10.5281/zenodo.10693 +6851 + + + + + +diastematum +Moffett + + + + + +Myrmoteras diastematum Moffett +, 1985: 36, figs 26. 29. + +Holotype +worker, E- +Malaysia +, + +Sarawak + +, 4th Division, Gunung Mulu National Park, camp 2, +v.-viii. 1978 +(P.M. Hammond and J.E. Marshall), +BMNH +[examined] + +. + + + +Diagnosis. TL 1.76, HL 1.12, HW 1.07, Cl 96, SL 1.28, SI 1.20, EL 0.68, El 64, ML 1.84. MI 164, PF5/4. + +The conspicuous sulcus between the clypeus and the frontal triangle and on the frons, and the long erect hairs (up to +0.25 mm +) are unique to this species. + + + + +Material examined: + +9 workers +, E- +Malaysia +, Kibongal Valley, +700 m +, +20.v. 1987 +(D.H. Burckhardt and I. +Loebl +), sifting of vegetational debris in a wooded gully close to fields, +BMNH +. +DAAC +, +MHNG + +. + + + + \ No newline at end of file diff --git a/data/38/8C/DB/388CDB66471336DE6A93C22F34F2223A.xml b/data/38/8C/DB/388CDB66471336DE6A93C22F34F2223A.xml new file mode 100644 index 00000000000..e95751dc241 --- /dev/null +++ b/data/38/8C/DB/388CDB66471336DE6A93C22F34F2223A.xml @@ -0,0 +1,109 @@ + + + +Coastal Fishes of Sao Tome and Principe islands, Gulf of Guinea (Eastern Atlantic Ocean) - an update. + + + +Author + +Peter Wirtz + + + +Author + +Carlos Eduardo L. Ferreira + + + +Author + +Sergio R. Floeter + + + +Author + +Ronald Fricke + + + +Author + +Joao Luiz Gasparini + + + +Author + +Tomio Iwamoto + + + +Author + +Luiz Rocha + + + +Author + +Claudio L. S. Sampaio + + + +Author + +Ulrich K. Schliewen + +text + + +Zootaxa + + +2007 + +1523 + + +1 +48 + + + + +http://www.zoobank.org/urn:lsid:zoobank.org:pub:2202520B-A3E7-492D-A932-14463CD6DAF9 + +journal article +z01523p001 +2202520B-A3E7-492D-A932-14463CD6DAF9 + + + + +Nicholsina usta (Valenciennes, 1840) + + + + +UFES 160 (1 specimen) from the fish market in +Sao +Tome +City. Encountered over a dense growth of +Caulerpa +sp. near +Ilheu +das Cabras in about 10 m depth (SMNS 25233, 1 specimen). The eastern Atlantic +Nicholsina usta +are generally considered to form the subspecies +N. usta collettei Schultz, 1968 +. Two animals from +Sao +Tome +analysed by Robertson et al. (2006) were genetically distinct from four western Atlantic animals to such a degree that the authors suggested the recognition of the two subspecies as valid species. + + + + \ No newline at end of file diff --git a/data/38/8D/54/388D54D70381E57AADC44C3CBF9838D3.xml b/data/38/8D/54/388D54D70381E57AADC44C3CBF9838D3.xml new file mode 100644 index 00000000000..8fe325803b0 --- /dev/null +++ b/data/38/8D/54/388D54D70381E57AADC44C3CBF9838D3.xml @@ -0,0 +1,51 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Cimex pini +[ +spec. nov. +] + + + + +C. oblongus ater, elytris fuscis macula rhombea nigra. +Fn. svec. +674. + + + + +Habitat in +Pinetis. + + + + \ No newline at end of file diff --git a/data/38/8D/5D/388D5D2DF37843CA4F7D57075374396C.xml b/data/38/8D/5D/388D5D2DF37843CA4F7D57075374396C.xml new file mode 100644 index 00000000000..8f149bae573 --- /dev/null +++ b/data/38/8D/5D/388D5D2DF37843CA4F7D57075374396C.xml @@ -0,0 +1,141 @@ + + + +Order Dasyuromorphia + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +22 +37 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Thylacinus cynocephalus +(Harris 1808) + + + + + + + +[Didelphis] cynocephala +Harris 1808 + +, +Trans. Linn. Soc. Lond., 9: 174 + +. + + + + +Type Locality: + +Australia +, +Tasmania +. + + + + + +Vernacular Names: +Thylacine +. + + + + +Synonyms: + +Thylacinus breviceps +Krefft 1868 + +; + +Thylacinus communis +Anon. 1859 + +; + +Thylacinus harrisii +Temminck 1824 + +; + +Thylacinus lucocephalus +(Grant 1831) + +; + +Thylacinus striatus +Warlow 1833 + +. + + + + +Distribution: +Tasmania +. + + + + +Conservation: +CITES +– Appendix I [Possibly Extinct]; +U.S. +ESA +– Endangered; +IUCN +– Extinct. + + + + +Discussion: +Probably extinct; but tracks and sightings continue to be reported; see +Ride (1970:201) +and Rounsvell and Smith (1982). Species reviewed by Guiler (1986) and +Paddle (2000) +. + + + + \ No newline at end of file diff --git a/data/38/8D/6B/388D6B6B2302480A9124665B13D49FEA.xml b/data/38/8D/6B/388D6B6B2302480A9124665B13D49FEA.xml new file mode 100644 index 00000000000..ac2521603db --- /dev/null +++ b/data/38/8D/6B/388D6B6B2302480A9124665B13D49FEA.xml @@ -0,0 +1,103 @@ + + + +Targeting a portion of central European spider diversity for permanent preservation + + + +Author + +Candek, Klemen + + + +Author + +Gregoric, Matjaz + + + +Author + +Kostanjsek, Rok + + + +Author + +Frick, Holger + + + +Author + +Kropf, Christian + + + +Author + +Kuntner, Matjaz + +text + + +Biodiversity Data Journal + + +2013 + +1 + + +980 +980 + + + + +http://dx.doi.org/10.3897/BDJ.1.e980 + +journal article +http://dx.doi.org/10.3897/BDJ.1.e980 +1314-2828--980 + + + + +Neoscona adianta (Walckenaer, 1802) + + + +Materials + + +Occurrence: recordedBy: + +Gregoric +, +Candek + +; sex: +1 female +; Location: locationID: SI53; country: +Slovenia +; locality: + +Dinaric Karst, +Grize + +; minimumElevationInMeters: 434; maximumElevationInMeters: 434; decimalLatitude: +45.7548 +; decimalLongitude: +13.9495 +; Event: eventDate: +2011-05-10 +/ +2011-06-21 +; habitat: grassland + + + + + \ No newline at end of file diff --git a/data/38/8D/B0/388DB0C93C5CDE0956759B3226A00DDD.xml b/data/38/8D/B0/388DB0C93C5CDE0956759B3226A00DDD.xml new file mode 100644 index 00000000000..7251f328366 --- /dev/null +++ b/data/38/8D/B0/388DB0C93C5CDE0956759B3226A00DDD.xml @@ -0,0 +1,63 @@ + + + +Descriptions de nouvelles fourmis Ethiopiennes. (Suite.) + + + +Author + +Santschi, F. + +text + + +Revue de Zoologie et de Botanique Africaines + + +1928 + +16 + + +191 +213 + + + + +http://antbase.org/ants/publications/3630/3630.pdf + +journal article +3630 + + + + +31. - +Monomorium (Xeromyrmex) termitarium For. st. disertum +(Forel). + + + + +( +M. salomonis v. diserta Forel +1913, Deutsch. Ent. Zeitschr., p. 2 i 6. Arnold, 1916, Ann. South Afr. Mus., XIV, p. 221. + + +M. salomonis st. termitarium v. diserta +. Forel 1916, Rev. Suisse Zool, XXIV, p. 417. - G. Arnold, 1926. Ann. South Afr. Mus., XXIII, p. 229). + + + + +Cette forme differe nettement de +termitarium +, par sa tete plus rectangulaire. D'autre part elle s'eloigne sensiblement de +salomonis +L. + + + + \ No newline at end of file diff --git a/data/38/8E/8C/388E8C917F4E50DFB4751E3EC3ED700B.xml b/data/38/8E/8C/388E8C917F4E50DFB4751E3EC3ED700B.xml new file mode 100644 index 00000000000..5cb4ffbab96 --- /dev/null +++ b/data/38/8E/8C/388E8C917F4E50DFB4751E3EC3ED700B.xml @@ -0,0 +1,285 @@ + + + +Caribbean Amphipoda (Crustacea) of Panama. Part II: parvorder Hadziidira + + + +Author + +White, Kristine N. +https://orcid.org/0000-0002-5203-1656 +Georgia College & State University, Department of Biological and Environmental Sciences, Aquatic Sciences Center, Milledgeville, GA 31061, USA +kristine.white@gcsu.edu + + + +Author + +Sir, Sally J. +https://orcid.org/0000-0002-1270-1192 +Georgia College & State University, Department of Biological and Environmental Sciences, Aquatic Sciences Center, Milledgeville, GA 31061, USA + +text + + +ZooKeys + + +2024 + +2024-03-18 + + +1195 + + +249 +296 + + + + +http://dx.doi.org/10.3897/zookeys.1195.116721 + +journal article +http://dx.doi.org/10.3897/zookeys.1195.116721 +1313-2970-1195-249 +4868E773FA184196B2075A691987CC8C +AD46D7C8FCCB5CB4AD7A21EC55516779 + + + + +Dulichiella lecroyae Lowry & Springthorpe, 2007 + + + + +Figs 18 +, 29D + + + + +Melita fresnelli + +Melita fresnelli + +Kunkel 1910 +: 31-34, fig. 11; +Pearse 1912 +: 371. + + +Dulichiella +sp. A: +LeCroy 2000 +: 78, fig. 126. + + +Dulichiella lecroyae +Lowry & Springthorpe, 2007: 34-38, figs 25-28. + + + +Material examined. + + +Panama +• +5-10 mm +• +1 ♂ +, +1 ♀ +; +Bocas del Toro +, +Swan Cay +; +9.453333°N +, +82.298333°W +; depth + +2-3 m + +, in orange sponge; +4 Aug 2005 +; +S. DeGrave +leg.; GCRL 6649 • +4 ♂ +, +1 ♀ +; +Bocas del Toro +, Crawl Cay; +9.250467°N +, +82.131617°W +; depth + +10 m + +, in sponge; +7 Aug 2005 +; +S. DeGrave +leg.; GCRL 6650 • +1 ♀ +; +Bocas del Toro +, Punta Caracol; depth + +1 m + +, in + +Lissodendoryx columbiensis + +sponge, +9 June 2009 +; +K. Hultgren +leg.; GCRL 6651 • +5 ♂ +, +4 ♀ +; +Bocas del Toro +, STRI Point; +9.34872°N +, +82.26258°W +; depth + +12 m + +, among coral rubble, +6 Aug 2021 +; +K.N. White +leg.; USNM 1703533• +1 ♂ +, +3 ♀ +; +Bocas del Toro +, Juan Point; +9.3015°N +, +82.29404°W +; depth + +10 m + +, among coral rubble, +7 Aug 2021 +; +K.N. White +leg.; USNM 1703534 • +12 ♂ +, +5 ♀ +; Drago; +9.418056°N +, +82.3375°W +; depth + +2-3 m + +, among coral rubble, +9 Aug 2021 +; +K.N. White +leg.; USNM 1703535 • +1 ♀ +; +Bocas del Toro + +, + +San Cristobal +; +9.2625°N +, +82.235°W +; depth + +15 m + +, among coral rubble, +10 Aug 2021 +; +K.N. White +leg.; USNM 1703536 • +1 ♂ +; +Bocas del Toro +, Pandora; +9.327769°N +, +82, 222207°W +; depth + +10 m + +, among coral rubble, +10 Aug 2021 +; +K.N. White +leg.; USNM 1703537 • +1 ♂ +; +Bocas del Toro +, Crawl Cay; +9.2376°N +, +82.1438°W +; depth + +1.5-3 m + +, among coral rubble, +11 Aug 2021 +; +K.N. White +leg.; USNM 1703538 + +. + + + +Diagnosis. +Gnathopod 1 coxa anteroventral corner not produced, anterior margin straight. Gnathopod 2 propodus distolateral crown with four rounded or subacute spines; dactylus apically hooked, fitting into posterodistal corner of propodus. Pereopods 6 and 7 carpus and propodus without bunches of long slender setae. Epimeron 1 posteroventral corner subquadrate; epimeron 3 posterodistal margin smooth. + + +Distribution. + +U.S.A.: Gulf of Mexico, South Florida, Cedar Keys, Dry Tortugas, South Carolina, Georgia ( +LeCroy 2000 +; +Lowry and Springthorpe 2007 +); Bermuda: Flatts Village, Castle Harbor, Harrington Sound ( +Kunkel 1910 +); Panama: Bocas del Toro (present study). + + + +Ecology and remarks. +These amphipods are associated with sponges and coral rubble at depths of 0-12 m. Panamanian specimens closely resemble previously described specimens, with slight variation in the anteroventral margin of the head. Panamanian specimens show a minutely bifid notch rather than a single acute point. + + +Figure 18. + +Dulichiella lecroyae + +, male, 3.6 mm, pereopods 6 and 7, epimeron and urosome, gnathopod 2 lateral, head, coxa 1. Scale bars: 0.5 mm. + + + + + \ No newline at end of file diff --git a/data/38/8E/97/388E97575C5A8797D92B99FF9822188C.xml b/data/38/8E/97/388E97575C5A8797D92B99FF9822188C.xml new file mode 100644 index 00000000000..c8b6f413634 --- /dev/null +++ b/data/38/8E/97/388E97575C5A8797D92B99FF9822188C.xml @@ -0,0 +1,100 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part O) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +696 +717 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Othonna sibirica +Linnaeus + +, + +Species Plantarum +2 + +: 924. 1753 + + +. + + + +"Habitat in Sibiria." RCN: 6362. + + + +Basionym of: + +Cineraria sibirica +(L.) L. (1763) + +. + + + + + + +Lectotype + +(Nordenstam & Illarionova in +Taxon +54: 141, f. 2. 2005): Herb. Linn. No. 348.13 ( +S +) + +. + + + + +Current name: + + +Ligularia sibirica + +(L.) Cass. + +( +Asteraceae +). + + + + \ No newline at end of file diff --git a/data/38/8E/B1/388EB16A391004ABBAB274A60F626B61.xml b/data/38/8E/B1/388EB16A391004ABBAB274A60F626B61.xml new file mode 100644 index 00000000000..80f043825c4 --- /dev/null +++ b/data/38/8E/B1/388EB16A391004ABBAB274A60F626B61.xml @@ -0,0 +1,102 @@ + + + +Catalogue of Geadephaga (Coleoptera, Adephaga) of America, north of Mexico + + + +Author + +Bousquet, Yves +Agriculture and Agri-Food Canada, Central Experimental Farm, Ottawa, Ontario, Canada +bousquety1@yahoo.com + +text + + +ZooKeys + + +2012 + +2012-11-28 + + +245 + + +1 +1722 + + + + +http://dx.doi.org/10.3897/zookeys.245.3416 + +journal article +http://dx.doi.org/10.3897/zookeys.245.3416 +1313-2970-245-1 +FFFF52503A0AFF882450FFB66D45FF8E +578462 + + + + +Brachinus fumans (Fabricius, 1781) + + + + +Carabus fumans +Fabricius, 1781: 307. Type locality: +"America" +(original citation), restricted to "Springfield [Hampden County], Mass[achusetts]" by Lindroth (1969a: 1105). Lectotype (♂), designated by Lindroth (1969a: 1105), in ZMUC. + + +Brachinus cyanopterus +LeConte, 1844: 49. Type locality: "New York" (original citation). Lectotype (♀), designated by Erwin (1970a: 134), in MCZ [# 5847]. Synonymy established by LeConte (1846b: 203), confirmed by Erwin (1970a: 134). + + +Brachinus sufflans +LeConte, 1846b: 204. Type locality: "NovEboraci [= New York]" (original citation). Lectotype (♀), designated by Erwin (1970a: 134), in MCZ +[ +# 5648]. Synonymy established by Chaudoir (1868b: 292), confirmed by Erwin (1970a: 134). + + +Brachinus affinis +LeConte, 1846b: 204. Type locality: "Indiana ad flumen Ohio" (original citation). Lectotype (♂), designated by Erwin (1970a: 134), in MCZ [# 31881]. Synonymy established with doubt by Chaudoir (1868b: 292), confirmed by Erwin (1970a: 134). + + +Brachinus amplipennis +Bates, 1891a: 268. Type locality: "Paso del Norte, Chihuahua [Mexico]" (lectotype label). Lectotype (♀), designated by Erwin (1970a: 136), in BMNH. Synonymy established by Lindroth (1969a: 1105) based on +Erwin's +(1969c) thesis. + + +Brachinus tabasconus +Bates, 1891a: 268. Type locality: "San Juan Bautista, Tabasco [Mexico]" (lectotype label). Lectotype (♂), designated by Erwin (1970a: 136), in BMNH. Synonymy established by Lindroth (1969a: 1105) based on +Erwin's +(1969c) thesis. + + +Brachinus atbarae +Stehr, 1950: 102. Type locality: "Atbara, B[ritish] C[olumbia]" (original citation). Holotype (♂) in OSUO. Synonymy established by Lindroth (1969a: 1105) based on +Erwin's +(1969c) thesis. + + + +Distribution. +This widely distributed species ranges from southwestern New Brunswick (Webster and Bousquet 2008: 23) to south-central British Columbia, south to southwestern California, the state of Tabasco in Mexico, and central Florida [see Erwin 1970a: Fig. 369]. + + +Records. + +CAN +: AB, BC, MB, NB, ON, QC +USA +: AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY - Mexico + + + + \ No newline at end of file diff --git a/data/38/8E/CA/388ECAC198C9EE2E2ACED2D8FEB54BD4.xml b/data/38/8E/CA/388ECAC198C9EE2E2ACED2D8FEB54BD4.xml new file mode 100644 index 00000000000..829060dd8b1 --- /dev/null +++ b/data/38/8E/CA/388ECAC198C9EE2E2ACED2D8FEB54BD4.xml @@ -0,0 +1,188 @@ + + + +Flora der Schweiz und angrenzender Gebiete. Band 1. Pteridophyta bis Caryophyllaceae (2 nd edition): Registerzuband 1 + + + +Author + +Hess, Hans Ernst + + + +Author + +Landolt, Elias + + + +Author + +Hirzel, Rosmarie + +text + +1972 +Birkhaeuser Verlag + + +https://doi.org/10.5281/zenodo.291815 + +book +291815 +10.5281/zenodo.291815 +3-7643-0843-5 + + + +<subSubSection id="C8FB6424222BADF41A8C42E78F62E1F8" pageId="null" pageNumber="677" type="nomenclature"> +<paragraph id="A4DE8A5A823DE66F41A7AB51A697D842" pageId="null" pageNumber="677"> +<taxonomicName id="D709BAD4B9A37B9D6BBBBEC0A7BD42A1" authority="L." class="Ascidiacea" family="Polycitoridae" genus="Salix" kingdom="Animalia" order="Aplousobranchia" pageId="null" pageNumber="677" phylum="Chordata" rank="species" species="cinerea"> +<pageBreakToken id="05118D3D228287AF1FF508942A50111E" pageId="null" pageNumber="677">Salix</pageBreakToken> +<normalizedToken id="147B16AAB78F3E18D68386EC5C999CAB" originalValue="cinérea" pageId="null" pageNumber="677">cinerea</normalizedToken> +<authorityName id="A0B31C6906A1FB79706DFAC0AB92AE57" pageId="null" pageNumber="677">L.</authorityName> +</taxonomicName> +</paragraph> +</subSubSection> +<subSubSection id="4D6DBD95C18FD90014C9E9AB745E4D8A" pageId="null" pageNumber="677" type="vernacular_names"> +<paragraph id="891F2ED72230527A579500EB45A065A5" pageId="null" pageNumber="677">Grau-Weide</paragraph> +</subSubSection> + + + +Strauch, selten Baum (bis 6 m hoch). 1 +jaehrige +Zweige graubraun, +aeltere +dunkelbraun, + +auch die 2 +jaehrigen +noch kraus behaart; + +Holz der 2-4 +jaehrigen +Zweige + +mit 1-2 cm langen, in frischem Zustande 0,2-0,5 mm hohen, scharfen +Laengsrippen + +(Rinde abheben!). +Blaetter +4-12 cm lang, meist +2 +- +3mal so lang wie breit +, oval, mit der +groessten +Breite meist +ueber +der Mitte, an der Spitze kurz zugespitzt oder abgerundet, oberseits flaumig behaart, +gegen den Rand +hin mit deutlich eingesenktem Nervennetz, +graugruen +bis +braungruen +(oliv), stets matt, unterseits auf den Nerven dicht flaumig behaart, dazwischen lockerer behaart (Epidermis sichtbar), Nervennetz vorstehend wie bei + +S. appendiculata + +(Nr. 30), +graugruen +bis +blaugruen +, beiderseits ohne Glanz, Rand nach unten umgebogen, + +fein bis grob, +unregelmaeβig +gezaehnt +oder wellig oder glatt; + +Blattstiel bis 1 cm lang. +Nebenblaetter +(meist vorhanden) bis 0,5 cm lang, meist +halbherzfoermig +, +gezaehnt +oder ganzrandig. +Bluetenstaende +erscheinen vor den +Blaettern +. +Tragblaetter +dunkelbraun bis schwarz, nur am Grunde hell, besonders am Rande dicht und lang behaart. +Staubfaeden +am Grunde dicht behaart, 2-4mal so lang wie das Tragblatt; + +Staub- +beutel +vor dem Platzen orangerot. + +Reife +Fruechte +bis 10 mm lang, +dicht stehend +( + +Bluetenstandsachse +meist nicht sichtbar + +), dicht filzig behaart; Stiel 1- +11/2 +mal so lang wie das Tragblatt, nicht +zurueckgebogen +; Narben bis +gegen +die Mitte 2teilig; Abschnitte weiter oben nochmals 2 teilig, alle Abschnitte parallel, nicht spreizend. + + +Zytologische Angaben. 2n += +76: +Material aus botanischen +Gaerten +; Pollenmeiose normal, wahrscheinlich teilweise apomiktisch (Blackburn und Harrison 1924, Wilkinson 1944). Nilsson (1931) will + +S. cinerea + +als amphidiploiden Bastard aus + +S. viminalis + +x + +S. caprea + +experimentell hergestellt haben. + + +Standort. +Kollin, montan. Nasse, kalkfreie, tonige bis humose +Boeden +. Moore, an +Tuempeln +und +Graeben +, lichte +Waelder +, zeigt +Staunaesse +oder geringen +Wasserdurchfluss +an. + + +Verbreitung. Eurasiatische Pflanze: +Europa +( +nordwaerts +bis 67° NB), Nordwestafrika, West- und +Suedwestasien +(Persien, Turkestan). - Im ganzen Gebiet verbreitet, ziemlich +haeufig +. + + + + \ No newline at end of file diff --git a/data/38/8E/FE/388EFEC266BB5FC09014AE84E0CB7D34.xml b/data/38/8E/FE/388EFEC266BB5FC09014AE84E0CB7D34.xml new file mode 100644 index 00000000000..0fb22336757 --- /dev/null +++ b/data/38/8E/FE/388EFEC266BB5FC09014AE84E0CB7D34.xml @@ -0,0 +1,107 @@ + + + +Strong differentiation between amphibian communities on two adjacent mountains in the Upper Rio Pastaza watershed of Ecuador, with descriptions of two new species of terrestrial frogs + + + +Author + +Reyes-Puig 1,2, Juan Pablo +Unidad de Investigacion, Instituto Nacional de Bio-diversidad (INABIO), Quito, Ecuador + + + +Author + +Reyes-Puig 1,3,4, Carolina +Unidad de Investigacion, Instituto Nacional de Bio-diversidad (INABIO), Quito, Ecuador + + + +Author + +Franco-Mena 5,6, Daniela +Unidad de Investigacion, Instituto Nacional de Bio-diversidad (INABIO), Quito, Ecuador + + + +Author + +Jost 2, Lou +Unidad de Investigacion, Instituto Nacional de Bio-diversidad (INABIO), Quito, Ecuador + + + +Author + +Yanez-Munoz 1,2, Mario H. +Unidad de Investigacion, Instituto Nacional de Bio-diversidad (INABIO), Quito, Ecuador + +text + + +ZooKeys + + +2022 + +2022-01-10 + + +1081 + + +35 +87 + + + + +http://dx.doi.org/10.3897/zookeys.1081.71488 + +journal article +http://dx.doi.org/10.3897/zookeys.1081.71488 +1313-2970-1081-35 +40218EB45A244B0691B8402CBAFF9062 +EB35434016A458FC997D6E708136C163 + + + + +Pristimantis aff. tungurahua + + + + +Figure 25 + + + +Remarks. + +A specimen (DHMECN 14445) of body size of 21.04 mm was collected on a fern leaf 110 cm from the ground, in the montane forests of Machay Reserve at 2600 m elevation. This species is very similar to + +Pristimantis tungurahua + +found in nearby localities, such as the Cerro Candelaria Reserve, Naturetrek-Vizcaya Reserve and Chamana Reserve. However, the Machay +Reserve's +specimen differs in that it has patterns with white spots in the groin and ventral surfaces, as opposed to the red belly and dark colour of + +P. tungurahua + +. + + + +Figure 25. +Pristimantis +sp. aff. +Pristimantis tungurahua +(DHMECN 14445). Photograph by Mario H. +Yanez-Munoz + + + + + \ No newline at end of file diff --git a/data/38/8F/4D/388F4DC2FEB2501192FB44591B750571.xml b/data/38/8F/4D/388F4DC2FEB2501192FB44591B750571.xml new file mode 100644 index 00000000000..87c8be752a1 --- /dev/null +++ b/data/38/8F/4D/388F4DC2FEB2501192FB44591B750571.xml @@ -0,0 +1,65 @@ + + + +Synopsis of the tribe Stipeae (Poaceae) in Nepal + + + +Author + +Nobis, Marcin + + + +Author + +Gudkova, Polina D. + + + +Author + +Pendry, Colin A. + +text + + +PhytoKeys + + +2019 + +128 + + +97 +119 + + + + +http://dx.doi.org/10.3897/phytokeys.128.34637 + +journal article +http://dx.doi.org/10.3897/phytokeys.128.34637 +1314-2003-128-97 +CFE1800CC09C53E78AFCB0D1E6864E45 +3378135 + + + + +Orthoraphium Nees, Proc. Linn. Soc. Lond. 1: 94 (1841) + + + +Type. + + +Orthoraphium roylei + +Nees. + + + + \ No newline at end of file diff --git a/data/38/90/14/389014E6AE971748D11B87ECC16F7B96.xml b/data/38/90/14/389014E6AE971748D11B87ECC16F7B96.xml new file mode 100644 index 00000000000..648f904e83b --- /dev/null +++ b/data/38/90/14/389014E6AE971748D11B87ECC16F7B96.xml @@ -0,0 +1,555 @@ + + + +Info Flora Schweiz - Scrophulariaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/scrophulariaceae.html + +url + + + + + +Scrophularia umbrosa +Dumort. + + + + + + +Gefluegelte +Braunwurz + + + + + +Art ISFS: 382200 Checklist: 1042640 +Scrophulariaceae +Scrophularia +Scrophularia umbrosa Dumort. + + +Zusammenfassung + + + + +Artbeschreibung + +(nach +Lauber & al. 2018 +) + +: +60-120 cm +hoch. + +Staengel +mit 4 breit +gefluegelten +Kanten. +Blaetter +laenglich-eifoermig +, am Grund +verschmaelert +oder gerundet + +, gestielt, die oberen scharf und oft ungleich +gezaehnt +, kahl. +Blueten +wie bei + +S. nodosa +(Nr. 1737) + +, aber + +gruenlich +bis rotbraun + +. Honigschuppe (Staubblattrudiment) 1,5-3mal so breit wie lang, vorn ausgerandet. +Kelchzipfel +/- rund, mit breitem Hautrand +. Frucht +/- kugelig. + + + + +Bluetezeit + +(nach +Lauber & al. 2018 +) + +: 6-8 + + +Standort und Verbreitung in der Schweiz + +(nach +Lauber & al. 2018 +) + +: +Graeben +, Bachufer, +Schlammboeden +/ kollin-montan / CH + + + + +Verbreitung global + +(nach +Lauber & al. 2018 +) + +: Eurasiatisch + + + + +Oekologische +Zeigerwerte + +(nach +Landolt & al. 2010 +) + +4 + fw + 44-342.h.2n=26 + + + +Status + + + +Status IUCN +: Nicht +gefaehrdet + + + + + +Oekologie + + + +Lebensform +Mehrjaehriger +Hemikryptophyt + + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + + + + + + + + +
+2.1.4 - +Bachroehricht +( +Glycero-Sparganion +) +
+5.1.3 - Feuchter Krautsaum (Tieflagen) ( +Convolvulion +) +
+
+ + +fett + +Dominante Art, welche das Aussehen des Lebensraumes +mitpraegt + +Charakterart +Weniger strikt an den Lebensraum gebundene Art + + +
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +nass; fFeuchtigkeit stark wechselnd (mehr als ++/- +2 Stufen) +Lichtzahl LhalbschattigSalzzeichen--
Reaktionszahl Rneutral bis basisch (pH 5.5-8.5)Temperaturzahl T +kollin ( +Laubmischwaelder +mit Eichen) +
+Naehrstoffzahl +N + +naehrstoffreich + +Kontinentalitaetszahl +K +subozeanisch (hohe Luftfeuchtigkeit, geringe Temperaturschwankungen, eher milde Winter)
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Scrophularia umbrosa +Dumort. + + + + + + +Volksname Deutscher Name: + +Gefluegelte +Braunwurz + +Nom +francais +: + +Scrophulaire +ailee + +Nome italiano: +Scrofularia alata + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Scrophularia umbrosa Dumort. + + +Checklist 2017 + +382200
= +Scrophularia umbrosa Dumort. + + +Flora Helvetica 2001 + +1749
= +Scrophularia umbrosa Dumort. + + +Flora Helvetica 2012 + +1739
= +Scrophularia umbrosa Dumort. + + +Flora Helvetica 2018 + +1739
= +Scrophularia umbrosa Dumort. + + +Index synonymique 1996 + +382200
= +Scrophularia umbrosa Dumort. + + +SISF/ISFS 2 + +382200
= +Scrophularia umbrosa Dumort. + + +Welten & Sutter 1982 + +1470
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Status Indigenat +: Indigen + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein + + +Status Rote Liste national 2016 + + +Status IUCN +: Nicht +gefaehrdet + + + +Zusaetzliche +Informationen + +Kriterien IUCN: -- + + +Status Rote Liste regional 2019 + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Biogeografische RegionenStatusKriterien IUCN
Jura (JU) +nicht +gefaehrdet +(Least Concern) +
Mittelland (MP) +potenziell +gefaehrdet +(Near Threatened) +A4c; B2b(iii)
Alpennordflanke (NA) +potenziell +gefaehrdet +(Near Threatened) +C2a(i)
+Alpensuedflanke +(SA) +verschollen, vermutlich in der Schweiz ausgestorben (Critically Endangered, Probably Extinct)
+Oestliche +Zentralalpen (EA) +verschollen, vermutlich in der Schweiz ausgestorben (Critically Endangered, Probably Extinct)
Westliche Zentralalpen (WA) +stark +gefaehrdet +(Endangered) +C2a(i)
+
+ + +Status nationale +Prioritaet +/Verantwortung + + + + + + + +
+Keine nationale +Prioritaet +oder internationale Verantwortung +
+
+ +Schutzstatus + + + + + + +
Kein internationaler, nationaler oder kantonaler Schutz
+
+Status in sektoriellen Umweltpolitiken + + + + + + + +
+Umweltziele Landwirtschaft: +L - Leitartweitere Informationen
+
+
+
+
\ No newline at end of file diff --git a/data/38/90/95/3890957FEE4EE7A7E358D9FE73A59402.xml b/data/38/90/95/3890957FEE4EE7A7E358D9FE73A59402.xml new file mode 100644 index 00000000000..3bd375baaaa --- /dev/null +++ b/data/38/90/95/3890957FEE4EE7A7E358D9FE73A59402.xml @@ -0,0 +1,207 @@ + + + +The semi-aquatic freshwater earthworms of the genus Glyphidrilus Horst, 1889 from Thailand (Oligochaeta, Almidae) with re-descriptions of several species + + + +Author + +Chanabun, Ratmanee +Animal Systematics Research Unit, Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand + + + +Author + +Sutcharit, Chirasak +Animal Systematics Research Unit, Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand + + + +Author + +Tongkerd, Piyoros +Animal Systematics Research Unit, Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand + + + +Author + +Panha, Somsak +Animal Systematics Research Unit, Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand +somsak.pan@chula.ac.th + +text + + +ZooKeys + + +2013 + +2013-02-06 + + +265 + + +1 +76 + + + + +http://dx.doi.org/10.3897/zookeys.265.3911 + +journal article +http://dx.doi.org/10.3897/zookeys.265.3911 +1313-2970-265-1 +DCFC44484A604991B3F7DAEA77D03FE2 +E458246D0C01DA57FF9AF025FF9C8A29 +578136 + + + + +7. +Glyphidrilus annandalei Michaelsen, 1910 +Figs 9 +10 +Table 1 + + + + +Glyphidrilus annandalei +Michaelsen, 1910: 101.Type locality: India: Malabar Coast, Travancore, Coorg, Mysore, Calicut, Malapuram and Tiruvallur. +Cognetti 1911 +: 502, figs 11, 12. +Stephenson 1916 +: 349, +1921 +: 767, +1922 +: 387, +1923 +: 491. +Michaelsen 1918 +: 344, 346. + + +Glyphidrilus rarus +Rao, 1922: 64. Type locality: Sandy banks of the Harangi, Madapur (Coorg), and of the Cauvery, Dubari forests, Fraserpett (Coorg). + + +Glyphidrilus saffronensis +Rao, 1922: 66, fig. 4B, C. Type locality: Margins of pools in the forests of Dubari, Fraserpett (Coorg); river-beds of the Cauvery, Dubari (Coorg). + + +Glyphidrilus annandalei +- Jamieson, 1968: 393. +Brinkhurst and Jamieson 1971 +: 755, figs 13.3A-C. +Gobi and Vijayalakshmi 2004 +: 1443. + + + +Material examined. + +The specimen which closely matches the measurements and anatomical characters of the original description is designated herein as the lectotype ZMH V3600 ( +Fig. 9 +). The type locality of this species is Quilon, Travancore. +Paralectotype: +ZMH V3600.1 (7 adults and 16 juveniles) same locality with lectotype. +Additional reference specimens: +4 adults (ZMH V3601) from Calicut, Malapuram, Tiruvallur. 13 adults (ZMH V3607) from Malabar. 1 juvenile (ZMH V9173) from Narayan, Vordeviu Dicu. 2 juveniles (ZMH V9172) from Narayan, Vordeviu Dicu. 1 subadult (NHM 1922: 4: 20: 2) from banks of the Harngi, Madapur (Coorg). 1 juvenile (NHM 1922: 4: 20: 3) from Forests of Dubari, Fraserpett (Coorg). + +Lectotype designation proposed herewith is necessary to ensure the species is based on a complete adult earthworm. + + +Description of Lectotype. + +Dimensions: body length 161 mm. Body cylindrical in anterior part, quadrangular in transverse section behind clitellum. 201 segments. Body colour pale brown. Anus dorsal terminal. At posterior end dorsal surface considerably broader than the ventral. Clitellar +wi +on ventro-lateral part of clitellum in 27-33. Prostomium zygolobous. Dorsal pores absent. Clitellum annular in 14-39. Four pairs of setae per segment from 2, setal formula aa:ab:bc:cd:dd = 1.0:0.5:1.5:0.5:1.0 at segment 8. Female pores, male pores and spermathecal pores not visible. +Gm +laterally paired or asymmetrical on bc in 18-26 and 33, median unpaired on aa in 13-17. + + +Septa 5/6-8/9 thicker, 9/10-10/11 thick and 11/12 to the last segment thin. +Gi +small, globular within 8-9. Intestine enlarged from 15. Dorsal blood vessel anterior to 8. +He +in 8-11. +Np +distinguishable from segment 14 onwards. +Sv +in 9-12, with the +pair +in segment 12 larger than the others. +Ov +in 13. Testis in 10-11. Prostate and accessory glands absent. +Sc +in 13/14-16/17, four to six on each side per segment. + + + +Variation. + +The body lengths of type and non-type material 90-265 mm. 125-322 segments. +Wi +in 25, 26, 27- +1/232 +, 32, +1/233 +, 33, 35, 36, clitellum in 13, 14, 15, 16, 17, 18-35, 36, 37, 38, 39, 40, 41. + + + +Remarks. + +See +Table 1 +. + + +This +specieswas known from India: Malabar Coast, Travancore, Coorg, Mysore, Calicut, Malapuram and Tiruvallur, Gadana River, and tributaries in the buffer zone of Kalakkad-Mundanthurai Tiger Reserve from a sub basin of the river in the southern Western Ghats, Bangalore, and Bhadravatha and along the edge of Bhavani River, northern parts of Tamil Nadu, and southern parts of Karnataka, India. Sandy banks of the Harangi, Madapur (Coorg), and of the Cauvery, Dubari forests, Fraserpett (Coorg). + + + +Figure 9. +Morphology of the lectotype (ZMH V3600) of + +Glyphidrilus annandalei + +Michaelsen, 1910, showing the +A +external ventral and +B +internal dorsal views. + + + + +Figure 10. +Morphology of the paralectotype of + +Glyphidrilus annandalei + +Michaelsen, 1910, showing the +A +external ventral view of NHM 1922: 4: 20: 3, and +B +and +C +NHM 1922: 4: 20: 2 showing the +B +external ventral and +C +internal dorsal views. + + + + + \ No newline at end of file diff --git a/data/38/90/C1/3890C13DBB01D3E251D3A654B2DCF1DF.xml b/data/38/90/C1/3890C13DBB01D3E251D3A654B2DCF1DF.xml new file mode 100644 index 00000000000..6ac7acd73a8 --- /dev/null +++ b/data/38/90/C1/3890C13DBB01D3E251D3A654B2DCF1DF.xml @@ -0,0 +1,154 @@ + + + +Australian Assassins, Part II: A review of the new assassin spider genus Zephyrarchaea (Araneae, Archaeidae) from southern Australia + + + +Author + +Rix, Michael G. + + + +Author + +Harvey, Mark S. + +text + + +ZooKeys + + +2012 + +191 + + +1 +62 + + + + +http://dx.doi.org/10.3897/zookeys.191.3070 + +journal article +http://dx.doi.org/10.3897/zookeys.191.3070 +1313-2970-191-1 + + + + +Zephyrarchaea melindae Rix & Harvey +sp. n. +Figs 8E9H1424 + + + +Toolbrunup Assassin Spider + + +Type material. + +Holotype male: Stirling Range National Park, Mount Hassell, Western Australia, Australia, +34°22'41"S +, +118°04'15"E +, sifting elevated leaf litter under +Lepidosperma +sedges near summit, 726 m, 22.IV.2009, M. Rix (WAM T118986). + + +Paratypes: Allotype female and 1 juvenile, Toolbrunup Peak, +34°23'02"S +, +118°02'55"E +, sifting elevated leaf litter under low herbaceous shrubs near summit, 964 m, 10.IV.2009, M. Rix, H. Wood (WAM T97468DNA: TP-152-F/TP-153-J). + + + +Other material examined. +AUSTRALIA: Western Australia:Stirling Range National Park: same data as holotype, 2 juveniles (WAM T97467DNA: HA-150-J/HA-151-J). + + +Etymology. +The specific epithet is a patronym in honour of Dr Melinda Moir, in recognition of her contributions to biodiversity research, especially in the Stirling Range National Park of southern Western Australia. + + +Diagnosis. + +Zephyrarchaea melindae +can be distinguished from +Zephyrarchaea janineae +and +Zephyrarchaea mainae +by the absence of dorsal hump-like tubercles on the abdomen (Figs 14 +A-B +); from +Zephyrarchaea marae +sp. n., +Zephyrarchaea marki +, +Zephyrarchaea porchi +sp. n. and +Zephyrarchaea vichickmani +sp. n. by the shape of tegular sclerites 2-3, which do not project beyond the retro-distal rim of the tegulum (Figs 14 +D-E +); and from +Zephyrarchaea barrettae +sp. n. by the shape of the anterior margin of the diastema adjacent to the +'neck' +, which is straight (in females) or only slightly concave in lateral view (in males) (Figs 14 +A-B +cf. Figs 15 +A-B +). Females further distinguished from other known congeners by the combination of a spherical abdomen (Fig. 14A), shallow post-ocular depression in lateral view (Fig. 9H), taller carapace (CH/CL ratio> 1.70) (Figs 7, 14A) and straight, almost vertical anterior margin of the diastema adjacent to the +'neck' +(Fig. 14A). + +This species can also be distinguished from other genotyped taxa (see Fig. 3) by the following three unique nucleotide substitutions for COI and COII (n = 4): G(165), G(924), T(1533). + + +Description. + +Holotype male: Total length 3.15; leg I femur 2.37; F1/CL ratio 2.01. Cephalothorax dark reddish-brown; legs tan brown with darker annulations; abdomen mottled grey-brown and beige, with reddish-brown dorsal scute and sclerites (Fig. 14B). Carapace relatively short (CH/CL ratio 1.77); 1.18 long, 2.09 high, 1.18 wide; +'neck' +0.68 wide; highest point of pars cephalica (HPC) approaching posterior third of +'head' +(ratio of HPC to post-ocular length 0.62), carapace with shallow concave depression anterior to HPC; +'head' +not strongly elevated dorsally (post-ocular ratio 0.20) (Fig. 8E). Chelicerae with proximal brush and additional comb of accessory setae on anterior face of paturon (Fig. 14C). Abdomen 1.64 long, 1.23 wide; almost spherical in lateral profile, without dorsal hump-like tubercles; dorsal scute fused anteriorly to epigastric sclerites, extending posteriorly to cover anterior two-thirds of dorsal abdomen. Unexpanded pedipalp (Figs 14 +D-F +) pyriform, with broad, distally curved embolus supported by conductor sclerites 1-2; tegular sclerite 1 (TS 1) strongly curved, claw-like in prolateral view, with twisted, flattened and broadly rounded apex; TS 2-3 not projecting beyond retro-distal rim of tegulum. + + +Allotype female: Total length 3.54; leg I femur 2.50; F1/CL ratio 1.93. Cephalothorax dark reddish-brown; legs tan brown with darker annulations; abdomen mottled grey-brown and beige (Fig. 14A). Carapace relatively short (CH/CL ratio 1.86); 1.29 long, 2.41 high, 1.28 wide; +'neck' +0.78 wide; highest point of pars cephalica (HPC) approaching middle of +'head' +(ratio of HPC to post-ocular length 0.57), carapace with shallow concave depression anterior to HPC; +'head' +not strongly elevated dorsally (post-ocular ratio 0.19) (Fig. 9H). Chelicerae without accessory setae on anterior face of paturon. Abdomen 1.95 long, 1.51 wide; spherical in lateral profile, without dorsal hump-like tubercles. Internal genitalia (Fig. 14G) with cluster of ≤ 15 sausage-shaped spermathecae either side of gonopore, clusters widely separated along midline of genital plate. + + + +Distribution and habitat. + +Zephyrarchaea melindae +is known only from the summits of Toolbrunup Peak and nearby Mount Hassell, in the western Stirling Range National Park of southern Western Australia (west of Chester Pass) (Fig. 24). Specimens have been collected by beating and sifting sedges ( +Lepidosperma +sp.) and low shrubs in montane heathland habitats. + + + +Conservation status. + +This species is a short-range endemic taxon ( +Harvey 2002b +), with a maximum total range of less than 10 km2, and all known populations in the western Stirling Range National Park potentially threatened by fire, dieback disease (affecting montane vegetation) and climate change. + + + + \ No newline at end of file diff --git a/data/38/90/C7/3890C7F74C8EB94E6950E9CF7D90BC6E.xml b/data/38/90/C7/3890C7F74C8EB94E6950E9CF7D90BC6E.xml new file mode 100644 index 00000000000..2d2817e165c --- /dev/null +++ b/data/38/90/C7/3890C7F74C8EB94E6950E9CF7D90BC6E.xml @@ -0,0 +1,65 @@ + + + +Checklist of Fabaceae Lindley in Balaghat Ranges of Maharashtra, India + + + +Author + +Gore, Ramchandra + + + +Author + +Gaikwad, Sayajirao + +text + + +Biodiversity Data Journal + + +2015 + +3 + + +4541 +4541 + + + + +http://dx.doi.org/10.3897/BDJ.3.e4541 + +journal article +http://dx.doi.org/10.3897/BDJ.3.e4541 +1314-2828-3-4541 + + + + +Indigofera linnaei Ali, 1958 + + + +Materials + +Type status: +Other material +. Location: continent: Asia; country: +India +; countryCode: IN; stateProvince: Maharashtra; municipality: Ambajogai; locality: +Talni +; verbatimLatitude: 18° +44.131N +; verbatimLongitude: 76° +30.630E +; verbatimCoordinateSystem: degrees minutes; geodeticDatum: WGS84; Event: month: June-December; fieldNumber: RDG- 011; fieldNotes: Trailing/twining herbs; Record Level: institutionCode: +Wachland College of Arts & Science, Solapur (WCAS). + + + + \ No newline at end of file diff --git a/data/38/90/CA/3890CA0BAD3A5B3088FE3980C8F6DB9C.xml b/data/38/90/CA/3890CA0BAD3A5B3088FE3980C8F6DB9C.xml new file mode 100644 index 00000000000..2fd686787c8 --- /dev/null +++ b/data/38/90/CA/3890CA0BAD3A5B3088FE3980C8F6DB9C.xml @@ -0,0 +1,92 @@ + + + +Diversity pattern of insects from Macao based on an updated species checklist after 25 years + + + +Author + +Xian, Chunlan +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China + + + +Author + +Leong, Chi Man +Department of Life Sciences, Faculty of Science and Technology, Beijing normal university - Hong Kong Baptist University United International College, Zhuhai, China & Macao Entomological Society, Estrada Coronel Nicolau de Mesquita, Macao SAR, China + + + +Author + +Luo, Jiuyang +https://orcid.org/0000-0002-2748-9534 +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China + + + +Author + +Jia, Fenglong +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China + + + +Author + +Han, Hongxiang +Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, China +hanhx@ioz.ac.cn + + + +Author + +Xie, Qiang +https://orcid.org/0000-0001-6376-8808 +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China +xieq8@mail.sysu.edu.cn + +text + + +Biodiversity Data Journal + + +2024 + +2024-04-05 + + +12 + + +118110 +118110 + + + + +http://dx.doi.org/10.3897/BDJ.12.e118110 + +journal article +http://dx.doi.org/10.3897/BDJ.12.e118110 +1314-2828-12-e118110 +57B0CE31B4055266A115FC1275D70C79 + + + + +Erthesina fullo (Thunberg, 1783) + + + +Notes + +Pun and Batalha (1997) + + + + \ No newline at end of file diff --git a/data/38/91/33/3891335DD55D7D5F8C3E71C1E9BFFFBB.xml b/data/38/91/33/3891335DD55D7D5F8C3E71C1E9BFFFBB.xml new file mode 100644 index 00000000000..8d94db7b399 --- /dev/null +++ b/data/38/91/33/3891335DD55D7D5F8C3E71C1E9BFFFBB.xml @@ -0,0 +1,129 @@ + + + +Megafauna of the UKSRL exploration contract area and eastern Clarion-Clipperton Zone in the Pacific Ocean: Annelida, Arthropoda, Bryozoa, Chordata, Ctenophora, Mollusca + + + +Author + +Amon, Diva J + + + +Author + +Ziegler, Amanda F + + + +Author + +Drazen, Jeffrey C + + + +Author + +Grischenko, Andrei V + + + +Author + +Leitner, Astrid B + + + +Author + +Lindsay, Dhugal J + + + +Author + +Voight, Janet R + + + +Author + +Wicksten, Mary K + + + +Author + +Young, Craig M + + + +Author + +Smith, Craig R + +text + + +Biodiversity Data Journal + + +2017 + +5 + + +14598 +14598 + + + + +http://dx.doi.org/10.3897/BDJ.5.e14598 + +journal article +http://dx.doi.org/10.3897/BDJ.5.e14598 +1314-2828-5-14598 + + + + +cf. Muusoctopus morphospecies + + + +Materials + + +Type status: +Other material +. Occurrence: recordedBy: +Diva J. Amon, Amanda F. Ziegler +; individualCount: +1 +; behavior: On seafloor; occurrenceStatus: present; preparations: Imaged only; Taxon: taxonConceptID: cf. Muusoctopus morphospecies; scientificName: Muusoctopus sp.; kingdom: Animalia; phylum: Mollusca; class: Cephalopoda; order: Octopoda; family: Enteroctopodidae; genus: Muusoctopus; taxonRank: genus; scientificNameAuthorship: Gleadall, 2004; Location: waterBody: Pacific Ocean; stateProvince: Clarion-Clipperton Zone; locality: +UK Seabed Resources Ltd exploration contract area (UK-1) +; verbatimLocality: UK-1 Stratum B; maximumDepthInMeters: 4225; locationRemarks: RV Thompson Cruise TN319; decimalLatitude: +12.5788 +; decimalLongitude: +-116.6873 +; geodeticDatum: WGS84; coordinateUncertaintyInMeters: 25; Identification: identifiedBy: +Janet Voight, Diva J. Amon, Amanda F. Ziegler +; dateIdentified: 2015; identificationReferences: Voight, Janet R. "Observations of deep-sea octopodid behavior from undersea vehicles." American Malacological Bulletin 24.1 (2008): 43-50.; identificationRemarks: Identified only from imagery; identificationQualifier: cf.; Event: samplingProtocol: +Autonomous Underwater Vehicle +; eventDate: +2015-03-09 +; eventTime: 3:50; habitat: Abyssal polymetallic-nodule field; fieldNumber: Dive 6 (AV06); Record Level: language: en; institutionCode: +UHM +; datasetName: ABYSSLINE; basisOfRecord: HumanObservation + + + + +Notes +Finless, benthic octopod with two rows of arm suckers, head narrower than mantle, arms coiled aborally when still, extended into sediment when walking. Swimming is propelled by mantle jets, not by fins. Ventrum often darker than dorsum, but not necessarily. +Fig. 56 + + + \ No newline at end of file diff --git a/data/38/91/4A/38914AA3FF7A5B0184F5A55824A4CF38.xml b/data/38/91/4A/38914AA3FF7A5B0184F5A55824A4CF38.xml new file mode 100644 index 00000000000..6b0a89709af --- /dev/null +++ b/data/38/91/4A/38914AA3FF7A5B0184F5A55824A4CF38.xml @@ -0,0 +1,195 @@ + + + +Taxonomic studies of the ground beetle subgenus Falcinebria Ledoux & Roux, 2005 (Coleoptera, Carabidae, Nebria) from Honshu, Japan + + + +Author + +Sasakawa, Koji + +text + + +ZooKeys + + +2020 + +902 + + +37 +60 + + + + +http://dx.doi.org/10.3897/zookeys.902.46531 + +journal article +http://dx.doi.org/10.3897/zookeys.902.46531 +1313-2970-902-37 +5AC31314F5A241DDB4D661A4C1E0BD73 +A2BB0E8E582A5D449E8F7F3F51170356 + + + + +Nebria (Falcinebria) chugokuensis +sp. nov. +Figs 16 +, 34 + +, 35 Japanese name: +Chugoku-hime-marukubi-gomimushi + + + + + +Nebria reflexa +: + +Ueno +(1985) + +: 56 (part); +Nakane (1963b) +: 19 (part). + + +Nebria (Falcinebria) reflexa uenoi +: Yoshiake et al. (2011): 33 (part). + + + +Notes. + +This species is widely distributed in the +Chugoku +Mountains. It is readily distinguished from other species previously considered + +N. reflexa + +distributed in +Honshu +by the concavity of the ventral surface of the aedeagal apex. It is distinguished from + +N. hikosana + +, described from nearby northern +Kyushu +, by two pairs of setae on the ventral side of the sterna, versus one pair in + +N. hikosana + +. + + + +Description. + +Body length: ♂, 9.97-10.32 mm (mean ++/- +SD: 10.12 ++/- +0.13 mm, +n += 5); ♀, 10.69-11.75 mm (mean ++/- +SD: 11.22 ++/- +0.53 mm, +n += 3). PPW/EL: ♂, 0.312-0.324 (mean ++/- +SD: 0.320 ++/- +0.005, +n += 5); ♀, 0.305-0.317 (mean ++/- +SD: 0.313 ++/- +0.007, +n += 3). Ventral surface of aedeagal apex deeply concave. Dorsobasal lobe absent. Dorsomedian lobe absent. Dorsoapical lobe with the basal part protruding dorsally; the protrusion as long as and narrower than the right laterobasal lobe; apical portion directed anteroventrally. Right laterobasal lobe large, with the width from a ventral view wider than the width of the gonopore protrusion from a lateral view. Left laterobasal lobe large, with the width from a ventral view wider than the width of the gonopore protrusion from a lateral view. Right lateroapical lobe bifurcated at the middle, with one apex directed posterolaterally and the other directed anterolaterally; the posterolateral apex further bifurcated. Left lateroapical lobe bifurcated at the middle, with one apex directed posterolaterally and the other directed anterolaterally; the anterolateral apex further bifurcated. Ventrobasal surface without swellings adjoining the laterobasal lobes; ventrobasal swelling large, semispherical from a lateral view. + + + +Figures 31-35. +Right lateral ( +a +), ventral ( +b +), dorsal ( +c +), and posterodorsal ( +d +) views of the endophallus and left laterodorsal view of the dorsoapical lobe ( +e +) of + +Nebria + +spp. +31 + +N. dichotoma + +sp. nov., holotype male +32 + +N. dichotoma + +sp. nov., paratype male from the type locality +33 + +N. uenoi + +, male from the type locality +34 + +N. chugokuensis + +sp. nov., holotype male +35 + +N. chugokuensis + +, paratype male from +Sandan-kyo +. ac, concavity of aedeagal apex; remaining abbreviations are provided in Figures +17-21 +. + + + + +Type materials. + +Holotype: ♂ (NARO), Mount Azuma, +Hiwa-cho +, +Shobara-shi +, Hiroshima Prefecture, Japan, 27.vii.1976, S. Nakamura leg. Paratypes (NARO): 1♂, same description as the holotype; 2♂3♀, +Sandan-kyo +, +Akiota-cho +, Hiroshima Prefecture, Japan (1♂1♀, 30.v.1957, K. Baba leg.; 1♂1♀, 31.v.1957, K. Baba leg.; 31.v.1970, I. Okamoto leg.); 1♂, +Chomon-kyo +, Atou, Yamaguchi-shi, Yamaguchi Prefecture, Japan, 18.v.1975, K. Tanaka leg. + + + +Etymology. + +The specific name refers to the +Chugoku +Mountains, where this new species is distributed. + + + + \ No newline at end of file diff --git a/data/38/91/D0/3891D06FDD865B4FAEF54D96F7222DFB.xml b/data/38/91/D0/3891D06FDD865B4FAEF54D96F7222DFB.xml new file mode 100644 index 00000000000..c15f0dad287 --- /dev/null +++ b/data/38/91/D0/3891D06FDD865B4FAEF54D96F7222DFB.xml @@ -0,0 +1,97 @@ + + + +First checklist of the chrysidid wasps (Hymenoptera, Chrysididae) of Mongolia, with description of new species + + + +Author + +Rosa, Paolo +Via Belvedere 8 / d, I- 20881 Bernareggio (MB), Italy +https://orcid.org/0000-0003-2919-5297 + + + +Author + +Proshchalykin, Maxim Yu. +Federal Scientific Centre for East Asian Terrestrial Biodiversity, Far Eastern Branch of Russian Academy of Sciences, Vladivostok 690022, Russia +https://orcid.org/0000-0001-7870-8226 +proshchalikin@biosoil.ru + + + +Author + +Halada, Marek +Milady Horakove 74 37012 Ceske Budejovice, Czeck Republic + + + +Author + +Aibek, Ulykpan +National University of Mongolia, Ulaanbaatar 210646, Mongolia + +text + + +ZooKeys + + +2020 + +999 + + +49 +107 + + + + +http://dx.doi.org/10.3897/zookeys.999.58536 + +journal article +http://dx.doi.org/10.3897/zookeys.999.58536 +1313-2970-999-49 +34E6CD7AEAD146D4926A61683DFFC740 +917CDF077020599AB0CA822B3D80745A + + + + +Chrysis belokobylskiji Rosa, 2019 + + + + +Chrysis belokobylskiji +Rosa, 2019: 2. Holotype ♀; Kyrgyzstan: Naryn River near Karakolka (ZIN) (examined); paratypes: 2 ♀♀, 1 ♂ [Mongolia: Nogon-kub, N. Gobi; 50 km E of Ulaanbaatar, Tuul River; 40 km SW of Uliastay]) ( +pulchella +group). + + + +Material examined. + +Mongolia: +Umnugovi +, 1 ♀, Nogon-kub, N. Gobi, 1.VIII.1926, P. Kozlov (ZIN); +Tuv +, 1 ♂, 50 km E of Ulaanbaatar, Tuul River, 22.VI.2003, leg. JH (MHC); +Zavkhan +, 1 ♀, 40 km SW of Uliastay, dunes, 18.VII.2005, leg. JH (MHC). + + + +Distribution. + +Mongolia (Tuv, Umnugovi, Zavkhan); China (Qinghai), Kyrgyzstan, Tajikistan ( +Rosa 2019 +). + + + + \ No newline at end of file diff --git a/data/38/91/D5/3891D57A5EF28664DBEF763BA8C67CB3.xml b/data/38/91/D5/3891D57A5EF28664DBEF763BA8C67CB3.xml new file mode 100644 index 00000000000..1d5e6cc854d --- /dev/null +++ b/data/38/91/D5/3891D57A5EF28664DBEF763BA8C67CB3.xml @@ -0,0 +1,60 @@ + + + +The ground beetles (Coleoptera: Carabidae) of the Strandzha Mountain and adjacent coastal territories (Bulgaria and Turkey) + + + +Author + +Kostova, Rumyana + + + +Author + +Gueorguiev, Borislav + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8135 +8135 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8135 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8135 +1314-2828--8135 + + + + +Carabus (Eucarabus) ullrichi rhilensis Kraatz, 1876 + + + +Materials + + +Type status: +Other material +. Location: countryCode: BG; locality: +Primorsko +; Record Level: bibliographicCitation: Hieke & Wrase (1988: 17) + + + + + \ No newline at end of file diff --git a/data/38/92/01/389201D253CCDF0A090FC591728E8684.xml b/data/38/92/01/389201D253CCDF0A090FC591728E8684.xml new file mode 100644 index 00000000000..7fd4aeaa1b8 --- /dev/null +++ b/data/38/92/01/389201D253CCDF0A090FC591728E8684.xml @@ -0,0 +1,143 @@ + + + +Saproxylic beetles of the Po plain woodlands, Italy + + + +Author + +Stefanelli, Silvia + + + +Author + +Della Rocca, Francesca + + + +Author + +Bogliani, Giuseppe + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1106 +1106 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1106 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1106 +1314-2828-2-1106 + + + + +Phymatodes testaceus (Linneaus, 1958) + + + + +Callidium violaceum +Rossi, 1790 - +Fauna Europaea (2013) + + +Callidium italicus +Gmelin, 1790 - +Fauna Europaea (2013) + + +Callidium ruficollis +Fabricius, 1781 - +Fauna Europaea (2013) + + + +Materials + + +Type status: +Other material +. Occurrence: recordedBy: +Silvia Stefanelli +; individualCount: +1 +; lifeStage: +adult +; Taxon: taxonID: urn:lsid:faunaeur.org:taxname:114557; scientificName: Phymatodestestaceus; order: Coleoptera; family: Cerambycidae; genus: Phymatodes; scientificNameAuthorship: Linnaeus 1758; Location: country: +Italy +; stateProvince: Pavia; locality: +SIC "Boschi Siro Negri e Moriano" - BN1 +; verbatimElevation: 68 m; verbatimCoordinates: 32T 503258E 5007870N; verbatimCoordinateSystem: UTM WGS 84; decimalLatitude: +45.224312 +; decimalLongitude: +9.041499 +; georeferencedBy: Silvia Stefanelli; georeferenceProtocol: GPS; Identification: identifiedBy: Carlo Pesarini; dateIdentified: 2011 + + + + +Type status: +Other material +. Occurrence: recordedBy: +Silvia Stefanelli +; individualCount: +1 +; lifeStage: +adult +; Taxon: taxonID: urn:lsid:faunaeur.org:taxname:114557; scientificName: Phymatodestestaceus; order: Coleoptera; family: Cerambycidae; genus: Phymatodes; scientificNameAuthorship: Linnaeus 1758; Location: country: +Italy +; stateProvince: Pavia; locality: +SIC "Boschi Siro Negri e Moriano" - BN10 +; verbatimElevation: 76 m; verbatimCoordinates: 32T 504479E 5006332N; verbatimCoordinateSystem: UTM WGS 84; decimalLatitude: +45.210461 +; decimalLongitude: +9.057038 +; georeferencedBy: Silvia Stefanelli; georeferenceProtocol: GPS; Identification: identifiedBy: Carlo Pesarini; dateIdentified: 2011 + + + + +Ecological interactions + +Conservation status + +Least Concern ( +European Environment Agency 2013 +). + + + + +Distribution + +Albania, Austria, Belarus, Belgium, Bosnia and Herzegovina, Britain I., Bulgaria, Corsica, Crete, Croatia, Cyprus, Czech Republic, Danish mainland, Estonia, European Turkey, Finland, French mainland, Germany, Greek mainland, Hungary, Italian mainland, Latvia, Liechtenstein, Lithuania, Luxembourg, Macedonia, Moldova Republic of, Norwegian mainland, Poland, Portuguese mainland, Romania, Russia Central, Russia East, Russia North, Russia Northwest, Russia South, Sardinia, Sicily, Slovakia, Slovenia, Spanish mainland, Sweden, Switzerland, The Netherlands, Ukraine, Yugoslavia, East Palaearctic, Near East, Nearctic region, North Africa, Oriental region ( +Fauna Europaea 2013 +). + + + +Notes + +The species develops in the dead branches and dead logs of various broadleaves, mainly oak, and also in conifers. The larva makes characteristic borings in the bark and sapwood. The adult is crepuscular and attracted to light and sweet secretions ( +Alexander 2002 +). + + + + \ No newline at end of file diff --git a/data/38/92/12/38921260BCB248FB49FBE8E94CB3B88E.xml b/data/38/92/12/38921260BCB248FB49FBE8E94CB3B88E.xml new file mode 100644 index 00000000000..a9eebf73368 --- /dev/null +++ b/data/38/92/12/38921260BCB248FB49FBE8E94CB3B88E.xml @@ -0,0 +1,150 @@ + + + +Geophagus abalios, G. dicrozoster and G. winemilleri (Perciformes: Cichlidae), three new species from Venezuela. + + + +Author + +Hernan López-Fernández + + + +Author + +Donald C. Taphorn + +text + + +Zootaxa + + +2004 + +439 + + +1 +27 + + + + +http://www.zoobank.org/urn:lsid:zoobank.org:pub:0288D909-8064-4FFC-92EC-6FFB5FED25CD + +journal article +z00439p001 +0288D909-8064-4FFC-92EC-6FFB5FED25CD + + + + +[[ +Geophagus Heckel +]] + + + +Discussion + +We describe three species of +Geophagus +from the +“surinamensis complex” +, elevating the described species in the genus to fourteen, and the known Venezuelan species to six. The new species +Geophagus abalios +, +G. dicrozoster +and +G. winemilleri +are diagnosable from species outside the +G. surinamensis complex +by the lack of a complete infraorbital stripe (Figs. 1, 2), which can be absent ( +G. abalios +) or reduced to a preopercular mark ( +G. dicrozoster +, +G. winemilleri +). The combination of coloration and squamation characters distinguishes the three species from each other, and from the other seven described species within the +G. surinamensis complex +(Fig. 2). Lateral bar patterns have been used as diagnostic characters in other genera of Neotropical cichlids, notably +Mesonauta +(Kullander & Silfvergrip 1991; Schindler 1998) and +Apistogramma +(e.g. Kullander 1980). It is clear from the present paper that some species of +Geophagus +present well-defined and stable patterns of lateral bars, and these can be used as diagnostic characters. Color photographs of aquarium specimens suggest that double-bar patterns and the lack of a preopercular mark, as observed in +G. abalios +n. sp. +, occur together in yet undescribed species (e.g. Weidner 2000, +Geophagus sp. “Maicuru” +, +G. sp. “Porto Franco” +, + +G. sp. “ +Tapajos +Orange Head” + +). This apparent consistency may reflect underlying phylogenetic relationships within +Geophagus +, and may provide useful sets of characters for future phylogenetic analysis within the genus. + + + + +Although little is known of the ecology of +Geophagus abalios +and +G. dicrozoster +, it appears that they share many essential aspects of their biology. Field observations in the +Rio +Cinaruco (south-western Venezuelan llanos) indicate that both species are mouthbrooders(HLF unpubl). Both species are among the most abundant in samples from lagoon, or to a lesser extent, channel habitats over bare sandy bottoms, although they can be abundant in structured habitats with submerged wood or rocks (Arrington, 2002). On at least one occasion, +G. dicrozoster +was captured in rapids near the headwaters of the +Rio +Negro (K. Winemiller et al. unpubl.). Preliminary diet analyses indicate that, at least qualitatively, both species share a diet of benthic insect larvae dominated by chironomids (Diptera), trichopterans and ephemeropterans (HLF unpubl.). Given the great similarity of these species in overall morphology, color patterns, feeding modes, and probably reproductive behavior, it is remarkable that they seem to share the same habitats in an extensive manner. The ecology of +G. winemilleri +is almost entirely unknown: all of our available records and observations indicate that it inhabits black waters with sandy bottoms, and it probably is a “larvophilous” mouth brooder (Weidner 2000). + + +Geophagus abalios +and +G. dicrozoster +are sympatric in most of their known distribution, and frequently are found in the same habitats, particularly in the Cinaruco river, southern Apure State (HLF unpubl.). Their syntopy will probably be shown to be more extensive once they are distinguished in collections, where they are commonly referred to as +G. surinamensis +or +G. altifrons +(e.g. Mago-Leccia 1970; Machado-Allison 1987; 1993; Royero et al. 1992). The broad distribution of both species in the Orinoco basin suggests they should be as common in Colombia as they are in the Venezuelan portion of the basin. It is not clear from our current distributional knowledge whether the range of +G. abalios +and +G. dicrozoster +extends further south than the headwaters of the +Rio +Negro. The known distribution of +G. winemilleri +is restricted to the lower Casiquiare and the upper +Rio +Negro, but the species may be present in the +Rio +Ventuari drainage of the middle Orinoco basin (DCT and C. +Montana +unpubl.). The fish diversity of the middle Orinoco and its tributaries is poorly known, and further collections are needed to clarify whether +G. winemilleri +is present in the upper Casiquiare and upper-middle Orinoco region. +G. winemilleri +is known to occur in the middle +Rio +Negro (HLF pers. obs.). Weidner (2000) indicates that all aquarium imports come from the +Rio +Negro and refers to a case in which the species was caught in the Archipelago das Anavilhanas, just north of Manaus. Further taxonomic, phylogenetic and distributional studies in the +Rio +Negro will be necessary before a fruitful discussion of the biogeographic history of +Geophagus +in this region is possible. + + + + \ No newline at end of file diff --git a/data/38/92/21/389221D6407B2E1D40057269642580DB.xml b/data/38/92/21/389221D6407B2E1D40057269642580DB.xml new file mode 100644 index 00000000000..33190a7cdd0 --- /dev/null +++ b/data/38/92/21/389221D6407B2E1D40057269642580DB.xml @@ -0,0 +1,68 @@ + + + +Checklist of British and Irish Hymenoptera - Braconidae + + + +Author + +Broad, Gavin R. + + + +Author + +Shaw, Mark R. + + + +Author + +Godfray, H. Charles J. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8151 +8151 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8151 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8151 +1314-2828-4-8151 + + + + +Rogas luteus Nees, 1834 + + + + +testaceus +(Fabricius, 1798, +Ichneumon +) preocc. + + +testaceator +(Thunberg, 1824, +Ichneumon +) + + + + \ No newline at end of file diff --git a/data/38/92/3B/38923B5CF4E6ABC71684C106F346154D.xml b/data/38/92/3B/38923B5CF4E6ABC71684C106F346154D.xml new file mode 100644 index 00000000000..0b04af4b5f6 --- /dev/null +++ b/data/38/92/3B/38923B5CF4E6ABC71684C106F346154D.xml @@ -0,0 +1,1344 @@ + + + +Manual of North American Agromyzidae (Diptera, Schizophora), with revision of the fauna of the " Delmarva " states + + + +Author + +Lonsdale, Owen +Agriculture & Agri-Food Canada, 960 Carling Avenue, Ottawa, ON, K 1 A 0 C 6, Canada +neoxabea@hotmail.com + +text + + +ZooKeys + + +2021 + +2021-07-29 + + +1051 + + +1 +481 + + + + +http://dx.doi.org/10.3897/zookeys.1051.64603 + +journal article +http://dx.doi.org/10.3897/zookeys.1051.64603 +1313-2970-1051-1 +639E252D43924ABB910BCEA5D8AD2487 +BE8CC6847F645F61BB2F7A6BCF96FD64 + + + + +Agromyza albipennis Meigen + + + + +Figs 34 +, 143-146 + + + + +Agromyza albipennis +Meigen, 1830: 171. +Spencer 1969 +: 32; +Spencer and Steyskal 1986b +: 262; + +Cerny +et al. 2020 + +: 194. + + +Agromyza dubitata +Malloch, 1913a: 311. Frick 1953: 68 [as synonym +Agromyza reptans +Fallen +], 1957: 199 [as synonym +Agromyza nigripes +Meigen]. +Spencer and Steyskal 1986b +[syn.]. + + +Agromyza albo-hyalinata +Zetterstedt, 1848: 2742. +Griffiths 1963 +[synonymy]. + + +Agromyza albipennis fennica +Griffiths, 1963: 128. +Spencer 1976 +[synonymy]. + + + +Description. +Wing length 2.1-2.9 mm (♂), 2.5-3.5 mm (♀). Length of ultimate section of vein M4 divided by penultimate section: 0.6-0.8. Eye height divided by gena height: 3.6-5.6. First flagellomere relatively elongate with dorsoapical corner slightly pointed; velvety with small apical tuft of dense pale hairs (only distinct when viewed anteriorly). Fronto-orbital plate and parafacial slightly pronounced, curving under eye as cheek. Ocellar triangle reaching level of anterior ors, sides concave. + +Chaetotaxy +: Two ors, two or three ori (if three, anterior seta smaller). Four postsutural dorsocentrals, anterior two much shorter. Mid tibia with two posteromedial setae. + + +Colouration +: Body black with halter white and wing veins paler and fore knee sometimes very narrowly yellow. Calypter margin and hairs white. Faint greenish shine sometimes evident, mostly on abdomen. + + +Genitalia +: (Figs +143-146 +) Surstylus broad and triangular, entirely fused to epandrium, margin darkly pigmented, setae clustered at apex and inner margin with several medial to subapical tubercle-like setae. Inner lobe of hypandrium with furrows leading to base of setae. Postgonite small, flat, lobe-like. Halves of basiphallus converging to point of fusion at base; apices abruptly converging; right 1/2 with long membranous extension at midpoint. Distiphallus of " + +Agromyza nigripes + +-type" (capsule-shaped with subbasal opening for entry of ejaculatory duct, pronounced dorsobasal collar, and medial convolution), with sides parallel medially, one pair of elongate parallel dark ventromedial swellings, and a slightly broadened apical margin with inner surface minutely spinulose; slightly angled dorsally. + + + +Hosts. + +Poaceae +- + +Triticum aestivum + +(only known North American host), + +Agrostis + +, + +Arrhenatherum + +, + +Brachypodium + +, + +Bromus + +, + +Calamagrostis + +, + +Dactylis + +, + +Deschampsia + +, + +Festuca + +, + +Glyceria + +, + +Hordeum + +, + +Milium + +, + +Phalaris + +, + +Phalaroides + +( +Ellis 2021 +), + +Phleum + +, + +Poa + +, + +Secale + +, + +Setaria + +. In Europe, most commonly occurring on + +Phalaria arundinacea + +, + +Hordeum + +and + +Poa + +( +Spencer and Steyskal 1986b +; +Benavent-Corai et al. 2005 +). + + + +Distribution. + +Canada +: AB, BC, MB, NB*, NL, NS*, NT, NU*, ON, QC, SK*, YT*. +USA +: AK, CA, CO, DC*, IA, IL, MA, MD*, MI, NC*, NY, OH, PA*, SC*. Widespread in Palaearctic ( + +Cerny +et al 2020 + +). + + + +Type material. + + +Syntype +[ + +Agromyza albipennis + +]: Austria + +[not given] (1♀, NMW). [Not examined]. + + + +Syntype +[ + +Agromyza dubitata + +]: USA. MA + +: Beverly (1♀, USNM; two females reported in +Spencer and Steyskal 1986b +). + + + +Paratypes examined + +[ + + +Agromyza dubitata + +]: Canada. QC + +: Beaulieu, Ile de Montreal, 14.vii.1906 (1♀, USNM), Ottawa [illegible], Beaulieu, 20.vii.1912, +"13" +(1♀, USNM), Cottage Beaulieu, Beaulieu, 16.vii.1906, +"15" +(1♀, USNM), Cottage Beaulieu, Beaulieu, 21.viii.1906, +"19" +(1♀, USNM), Cottage Beaulieu, Beaulieu, 10.vi.1906, "21 0" (1♀, USNM). +USA. MA +: Beverly, 23.viii.1969 (1♀, USNM). + + + +Syntypes +[ + +Agromyza albo +- +Agromyza hyalinata + + +]: "Ovasa ad Esperod Scaniae +... +Dania" (? ZIL). [Not examined]. + + + +Holotype +[ + +Agromyza albipennis +Agromyza fennica + +]: Finland. + +Messuby (1♂, UZMH). [Not examined]. + + + +Additional material examined. + + + +Canada +. AB + +: +Black Foot Hills +, +9.viii.1940 +, +A.R. Brooks +, CNC352861 ( +1♀ +, CNC), Lethbridge, +27.vi.1923 +, +H.L. Seamans +, CNC352860 ( +1♀ +, CNC), +Banff Natl. Pk. +, Lk. Louise, + +1402 m + +, +7.vii.1955 +, +R. Coyles +, CNC352693 ( +1♀ +, CNC), Banff, Jasper Hwy, Sunwapta Pass, + +2011 m + +, +7.vii.1955 +, +R. Coyles +, CNC352692 ( +1♀ +, CNC), Elkwater, +11.vi.1956 +, CNC352652 ( +1♂ +, CNC), Onefour, +49°6'0"N +, +110°24'0"W +, +4.vi.1955 +, +J.R. Vockeroth +, CNC352653, CNC352654 ( +2♂ +, CNC), + +Elk Island +N.P. Wood Bison Trail + +wetland alongside aspen forest, lots of tall grass, +53.5666°N +, +112.8514°W +, + +722 m + +, BIOBus, +1.vii.2012 +, BIOUG06731-D05 ( +1♂ +, CNC), +Waterton Lakes NP +, Highway 6 pulloff east of 2 Flags Lookout montane forest, douglas fir and lodgepole pine (mostly conifer with aspen/birch understory), +49.065°N +, +113.7781°W +, + +1562 m + +, BIOBus, +11.viii.2012 +, BIOUG06502-C07 ( +1♀ +, CNC), +BC +: Liard Hot Spg. Mi496 +Alaska +Hwy, + +457 m + +, +9-10.vii.1959 +, +E.E. MacDougall +, CNC352698 ( +1♀ +, CNC), +Moosehorn Lake +, +58°10'0"N +, +132°7'0"W +, + +1371 m + +, +25.vii.1960 +, +R. Pilfrey +, CNC352658 ( +1♂ +, CNC), +Summit L. +, Mi392 +Alaska +Hwy, + +1402 m + +, +16.vii.1959 +, +E.E. MacDougall +, CNC352699 ( +1♀ +, CNC), Terrace, +10.vi.1960 +, +5.vi.1960 +, +C.H. Mann +, CNC352655, CNC352656, CNC352657, CNC352697 ( +3♂ +1♀ +, CNC), Vernon, +3.ix.1931 +, +R.D. Bird +, CNC352651, 2s37, IV 31 ( +1♂ +, CNC), Bobson, +6.v.1952 +, +H.R. Foxlee +, CNC352862 ( +1♀ +, CNC), Oliver, +20.v.1923 +, +C.B. Garrett +, CNC352863 ( +1♀ +, CNC), Vernon, +31.vii.1937 +, +H. Leech +, CNC352864 ( +1♀ +, CNC), Victoria, +20.v.1919 +, +W. Downes +, CNC352844 ( +1♂ +, CNC), +MB +: Minnedosa, +5mi +N, +8.vii.1958 +, +R.L. Hurley +, CNC352690 ( +1♀ +, CNC), Shilo, +5mi +SW, +28.v.1958 +, +R.B. Madge +, CNC352663 ( +1♂ +, CNC), +Western MB +, + + +Riding +Mountain Nat. Pk. - North Escarpment Trailhead + + +wet meadow/marsh, +50.674°N +, +99.65°W +, + +726 m + +, +J. Straka +, +J. Crossey +, +15.viii.2008 +, 08BDIP-1973 ( +1♀ +, CNC), Aweme, +26.vi.1916 +, +N. Criddle +, CNC352842 ( +2♂ +, CNC), +28.viii.1917 +, CNC352843 ( +1♂ +, CNC), +NB +: +Kouchibouguac N.P. +, +8.vii.1977 +, +J.F. McAlpine +, Code-6020N, CNC352688, CNC352689 ( +2♀ +, CNC), +NL +: Gros Morne; + +Gros Morne +Mountain Hiking Trail + +, +49.5657°N +, +57.8324°W +, + +39 m + +, +J. Crossey +, +R. Labbee +, +A. Smith +, +M. Zhang +, +15.vii.2009 +, 09BBEDI-0938 ( +1♀ +, CNC), + +St. +John's + +, Agric. Exp. Sta., +12.vii.1967 +, +15.vii.1967 +, +J.F. McAlpine +, CNC353033, CNC353041, CNC353042 ( +2♂ +1♀ +, CNC), +NS +: Kentville, +22.viii.1912 +, from tortricid larva on apple, [illegible], CNC352650 ( +1♂ +, CNC), +NT +: +Ft. McPherson +, +19.vii.1957 +, +R. Hurley +, CNC352695 ( +1♀ +, CNC), +NU +: [ +N.W.T. +] +Muskox L. +, +64°45'0"N +, +108°10'0"W +, +2.viii.1953 +, +J.G. Chillcott +, CNC352696 ( +1♀ +, CNC), +ON +: Almonte, +18.v.1951 +, +J.F. McAlpine +, CNC352679 ( +1♀ +, CNC), Hailerbury, +12.viii.1947 +, +G.S. Walley +, CNC352646 ( +1♂ +, CNC), Marmora, +1.vi.1952 +, +13.v.1952 +, +J.C. Mitchell +, +J.R. Vockeroth +, CNC352674, CNC352675, CNC352676 ( +3♀ +, CNC), Maynooth, +25.v.1951 +, +J.F. McAlpine +, CNC352677 ( +1♀ +, CNC), Minnedosa, +5mi +N, +8.vii.1958 +, +R.L. Hurley +, CNC352691 ( +1♀ +, CNC), Normandale, +42°42'0"N +, +80°19'0"W +, +27.v.1956 +, +J.R. Vockeroth +, CNC352645 ( +1♂ +, CNC), +29.v.1956 +, +J.R. Lonsway +, CNC352678 ( +1♀ +, CNC), Ottawa, +8.vii.1952 +, +G.E. Shewell +, CNC352647 ( +1♂ +, CNC), +Port Hope +, +25.v.1925 +, +N.K. Bigelow +, CNC352680 ( +1♀ +, CNC), +Port Severn +, +3mi +N, +18.v.1959 +, +J.G. Chillcott +, CNC352681 ( +1♀ +, CNC), Putnam, +26.vi.1925 +, +G.S. Walley +, CNC352644 ( +1♂ +, CNC), +St. Williams +, +42°40'0"N +, +80°25'0"W +, +23.v.1956 +, +J.R. Vockeroth +, CNC352649 ( +1♂ +, CNC), +Turkey Pt. +, +42°39'0"N +, +80°21'0"W +, +25.v.1956 +, +J.R. Vockeroth +, CNC352683 ( +1♀ +, CNC), Brockville, +5.viii.1903 +, +W. Metcalfe +, CNC352847 ( +1♀ +, CNC), Cottage Beaulieu, +16.vii.1906 +, 145, CNC352854 ( +1♀ +, CNC), Mer Bleue, +10.v.1938 +, +G.E. Shewell +, CNC352834 ( +1♂ +, CNC), Norway Point, +Lake of Bays +, +31.vii.1919 +, +J. McDunnough +, CNC352851 ( +1♀ +, CNC), Orillia, +18.vii.1923 +, +C.H. Curran +, CNC352848 ( +1♀ +, CNC), +17.viii.1923 +, CNC352850 ( +1♀ +, CNC), Ottawa, +15.vii.1938 +, +A. Brooks +, CNC352830 ( +1♂ +, CNC), Ottawa, +11.ix.1947 +, +G.E. Shewell +, CNC352829 ( +1♂ +, CNC), +Ottawa, A +. Brooks, +5.vii.1938 +, CNC352852 ( +1♂ +, CNC), Ottawa, +27.vii.1912 +, Beaulieu, CNC352853 ( +2♂ +2♀ +, CNC), +Pt. Ryerse +, +1.vi.1939 +, +G.E. Shewell +, CNC352835 ( +1♂ +, CNC), +St. Johns +, +Little Montreal River +, +9.vii.1937 +, +G.E. Shewell +, CNC352855 ( +1♀ +, CNC), Simcoe, +8.vi.1939 +, +G.E. Shewell +, CNC352849 ( +1♀ +, CNC), +Simcoe, G.E +. Shewell, +14.vi.1939 +, CNC352831 ( +1♂ +, CNC), +Simcoe, G.E +. Shewell, +22.vi.1939 +, CNC352832 ( +1♂ +, CNC), +Simcoe, G.E +. Shewell, +29.v.1939 +, CNC352833 ( +3♂ +1♀ +, CNC), Metcalfe, +2mi +N, +10.vi.1982 +, +B.E. Cooper +, CNC353037 ( +1♂ +, CNC), Metcalfe, +25.v.1983 +, +B.E. Cooper +, CNC353038 ( +1♂ +, CNC), Ottawa, damp second-growth +Acer +- +Betula +wood, +15.viii.2003 +, +20.vii.1974 +, +29.vi.1991 +, +J.R. Vockeroth +, CNC353032, CNC353035, CNC353036 ( +2♂ +1♀ +, CNC), +Port Severn +, +3mi +N, black spruce bog, +18.v.1959 +, +J.G. Chillcott +, CNC353039, CNC353034 ( +2♂ +, CNC), +QC +: + +Ile +de Montreal + +, +7.vii.1906 +, Beaulieu, CNC352837 ( +1♂ +, CNC), Old Chelsea, +13.vi.1961 +, +J.R. Vockeroth +, CNC353040 ( +1♂ +, CNC), +St. Johns +, +Little Montreal River +, +9.vii.1937 +, +G.E. Shewell +, CNC352836 ( +1♂ +, CNC), Wakefield, +9.vii.1946 +, +G.E. Shewell +, CNC352838 ( +1♂ +, CNC), Woburn, +19.vi.1923 +, +C.H. Curran +, CNC352859 ( +1♀ +, CNC), Aylmer, +16.vii.1959 +, +C.H. Mann +, CNC352684 ( +1♀ +, CNC), Farnham, +5.vi.1963 +, +J.R. Vockeroth +, CNC352642, CNC352682 ( +1♂ +1♀ +, CNC), Hull, +20.vi.1956 +, +J.R. Vockeroth +, CNC352685 ( +1♀ +, CNC), +Indian House L. +, +20.vii.1954 +, +27.vi.1954 +, +27.vii.1954 +, +R. Coyle +, +R. Coyles +, +W.R. Richards +, CNC352648, CNC352686, CNC352687 ( +1♂ +2♀ +, CNC), Knowlton, Bolton Pass, + +243 m + +, +5.vi.1963 +, +J.R. Vockeroth +, CNC352641 ( +1♂ +, CNC), +Mt. Orford +, + +365 m + +, +5.vi.1963 +, +J.R. Vockeroth +, CNC352643 ( +1♂ +, CNC), +Abbotsford, G +. Shewell, +29.v.1936 +, CNC352839, CNC352858 ( +1♂ +1♀ +, CNC), Abbotsford, +10.viii.1937 +, +G.E. Shewell +, CNC352840 ( +1♂ +, CNC), +Abbotsford, G +. Shewell, +20.viii.1936 +, CNC352841 ( +1♂ +, CNC), +30.v.1936 +, CNC352857 ( +1♀ +, CNC), Abbotsford, +20.v.1931 +, +J.B. Maltais +, CNC352856 ( +3♂ +3♀ +, CNC), +SK +: +Christopher L. +, +27.viii.1948 +, +A.R. Brooks +, CNC352705, CNC352706 ( +2♀ +, CNC), +Val Marie +, +49°15'0"N +, +107°44'0"W +, +5.vi.1955 +, +9.vi.1955 +, +J.R. Vockeroth +, CNC352659, CNC352662, CNC352664, CNC352665, CNC352666, CNC352700, CNC352701, CNC352702, CNC352703, CNC352704, CNC352707 ( +5♂ +6♀ +, CNC), +Grasslands National Park +, +Visitor's +Center grass cattle pasture, +49.246°N +, +107.732°W +, + +812 m + +, +J. Cossey +, +N. Jeffery +, +J. Straka +, +14.vii.2008 +, 08BBDIP-2742 ( +1♂ +, CNC), +Saskatoon +, +12.vii.1940 +, +22.vii.1939 +, +25.v.1926 +, +25.viii.1923 +, +28.ix.1925 +, sf. wheat, +A.P. Robinson +, +K.M. King +, +King +, 13288; D679; '41, 1328B; D676; '41, 1328B; D677, 1328B; D678, 16410- 3N9B, 16423 1229B; D348, 16425 26BS5; D350, 63AN, D663, CNC352845, CNC352846, CNC352865, CNC352866, CNC352867, CNC352868, CNC352869, CNC352870, CNC352871 ( +2♂ +7♀ +, CNC), +YT +: +Otter Lake +, + +1219 m + +, +15.vii.1960 +, +J.E. H. Martin +, CNC352694 ( +1♀ +, CNC) + +. + + +USA +. AK + +: Anchorage, +18.vi.1951 +, +3.vii.1951 +, IDEMA +Illustration, R.S +. Bigelow, CNC352668, CNC352720 ( +1♂ +1♀ +, CNC), Fairbanks, +13.vi.1952 +, +J.B. Bartley +, CNC352669 ( +1♂ +, CNC), Mackenzie Delta, Reindeer Depot, +30.vi.1948 +, +J.R. Vockeroth +, CNC352661 ( +1♂ +, CNC), Umiat, +13.vii.1959 +, +24.vii.1959 +, +5.vii.1959 +, +6.vii.1959 +, +7.vii.1959 +, +7.viii.1959 +, +9.viii.1959 +, IDEMA +Illustration, J.E.H +. +Martin, R +. Madge, CNC352660, CNC352667, CNC352673, CNC352712, CNC352713, CNC352714, CNC352715, CNC352716, CNC352717, CNC352718, CNC352719 ( +3♂ +8♀ +, CNC), +CO +: Walden, +11.viii.1965 +, +G.F. Knowlton +( +1♂ +, USNM), Doolittle Ranch, 9800', +Mt. Evans +, +9.vii.1961 +, +C.H. Mann +( +1♂ +, USNM), Doolittle Ranch, +Mt. Evans +, + +2987 m + +, +3.viii.1961 +, +9.vii.1961 +, +C.H. Mann +, CNC352670, CNC352708 ( +1♂ +1♀ +, CNC), Boulder, 5500', +5.vi.1961 +, +B.H. Poole +( +1♀ +, USNM), +Mt. Evans +, + +3535 m + +, +11.vii.1961 +, +C.H. Mann +, CNC352711 ( +1♀ +, CNC), +Mt. Evans +, + +3566 m + +, +22.vii.1961 +, +B.H. Poole +, CNC352710 ( +1♀ +, CNC), Nederland, + +2529 m + +, +5.vii.1961 +, +J.G. Chillcott +, CNC352672 ( +1♂ +, CNC), +Jackson Co. +, +Rabbit Ears Pass +, +7.vii.1961 +, +J.G. Chillcott +, CNC352671, CNC352709 ( +1♂ +1♀ +, CNC), +DC +: +Theo Roosevlt Id +, +4.vi.1977 +, +W.N. Mathis +( +1♂ +, USNM), +MA +: +Boston +, +June +( +1♂ +1♀ +, USNM), +Concord +, +19.vii.1961 +, marsh, +W.W. Wirth +( +2♂ +3♀ +, USNM), +Forest Hills +, +21.ix.1913 +, +A.L. Melander +( +2♀ +, USNM), +MD +: +Colesville +, +4.vii.1976 +, +W.W. Wirth +( +2♀ +, USNM), +Colesville +, +14.vi.1975 +, +Malaise trap +, +W.W. Wirth +( +1♀ +, USNM), +NC +: +Macon Co. +, +Highlands +, +Lake Ravenel +, +7.vi.1986 +, +Malaise trap +, +W.W. Wirth +( +1♂ +, USNM), +NY +: +Ithaca +, +15.viii.1926 +, +A.L. Melander +( +1♂ +, USNM), +Geneva +, +28.v.1914 +, +A.L. Melander +( +1♂ +, USNM), +Long Island +, +Cold Spring Harbor, A.L +. Melander ( +1♂ +2♀ +, USNM), +Allegany State park +, +28.v-3.vi.1963 +, mossy woods, +W.W. Wirth +( +1♀ +, USNM), +PA +: Mineral Spr., +5.ix.1927 +, +A.L. Melander +( +1♂ +, USNM), +Chester Co. +, +Avondale +, Stroud Res. Ctr., +28.ix.2006 +, +K. Styer +( +1♀ +, UDCC), +SC +: +Black Falls +, +7.viii.1953 +, +A.L. Melander +( +1♀ +, USNM) + +. + + + +Comments. + +See comments for + +Agromyza aprilina + +. + + + + \ No newline at end of file diff --git a/data/38/93/7B/38937B7C2E4058EDB96E89D2F0E45F7A.xml b/data/38/93/7B/38937B7C2E4058EDB96E89D2F0E45F7A.xml new file mode 100644 index 00000000000..b47ce321bee --- /dev/null +++ b/data/38/93/7B/38937B7C2E4058EDB96E89D2F0E45F7A.xml @@ -0,0 +1,77 @@ + + + +Checklist of national key protected wild plants on the Qinghai-Tibetan Plateau + + + +Author + +Chen, Ronglian +University of Chinese Academy of Sciences, Beijing, China & Qinghai Provincial Key Laboratory of Crop Molecular Breeding, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, China + + + +Author + +Zhang, Faqi +Qinghai Provincial Key Laboratory of Crop Molecular Breeding, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, China + + + +Author + +Chen, Shilong +Qinghai Provincial Key Laboratory of Crop Molecular Breeding, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, China + + + +Author + +Chi, Xiaofeng +Qinghai Provincial Key Laboratory of Crop Molecular Breeding, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, China +xfchi@nwipb.cas.cn + +text + + +Biodiversity Data Journal + + +2023 + +2023-05-16 + + +11 + + +103289 +103289 + + + + +http://dx.doi.org/10.3897/BDJ.11.e103289 + +journal article +http://dx.doi.org/10.3897/BDJ.11.e103289 +1314-2828-11-e103289 +D2D96D0A93125BF2BD8A1911FBE4E783 + + + + +Dendrobium chryseum Rolfe,1888 + + + +Conservation status +EN + + +Distribution +China + + + \ No newline at end of file diff --git a/data/38/94/13/3894136C383B503D8CEEE5FC9E0DBCFB.xml b/data/38/94/13/3894136C383B503D8CEEE5FC9E0DBCFB.xml new file mode 100644 index 00000000000..57f6114074c --- /dev/null +++ b/data/38/94/13/3894136C383B503D8CEEE5FC9E0DBCFB.xml @@ -0,0 +1,93 @@ + + + +Catalogue of the type material of Scarabaeoidea (Coleoptera) deposited in the Research Institute of Evolutionary Biology, Tokyo, Japan + + + +Author + +Kaneko, Naoki +Laboratory of Entomology, Tokyo University of Agriculture, 1737 Funako, Atsugi, Kanagawa, 243 - 0034, Japan +naoki.1993062z@gmail.com + + + +Author + +Wada, Kaoru +School of Science and Engineering, Meisei University, 2 - 1 - 1 Hodokubo, Hino, Tokyo 191 - 8506, Japan + +text + + +ZooKeys + + +2020 + +958 + + +35 +89 + + + + +http://dx.doi.org/10.3897/zookeys.958.52799 + +journal article +http://dx.doi.org/10.3897/zookeys.958.52799 +1313-2970-958-35 +101EE6D955804A4CB7C063FF9E2993A2 +48B3235B7EBF5310B8A9F2905C223E0F + + + + +Hoplia choui Miyake +Figure 3G + + + + +Hoplia choui +Miyake, 1986b: 203-204. + + + +Note. +The holotype is deposited in RIEB (ex coll. Y. Miyake): + + +Holotype + +(♂). +'Sozan / Formosa / 26. V. 1940 / Coll. M. Uno // HOLOTYPE / +Hoplia +/ Choui Y. MIYAKE / 1986'. (Fig. +3G +) + + + +Type condition. +Abdomen only. + + +Current status. +Valid species. + + +Remark. + +Most part of the holotype specimen was destroyed by + +Anthrenus verbasci + +. + + + + \ No newline at end of file diff --git a/data/38/94/1C/38941CC6A3C7B86E85FE89C442D00D61.xml b/data/38/94/1C/38941CC6A3C7B86E85FE89C442D00D61.xml new file mode 100644 index 00000000000..81c8f20b887 --- /dev/null +++ b/data/38/94/1C/38941CC6A3C7B86E85FE89C442D00D61.xml @@ -0,0 +1,130 @@ + + + +The " Martian " flora: new collections of vascular plants, lichens, fungi, algae, and cyanobacteria from the Mars Desert Research Station, Utah + + + +Author + +Sokoloff, Paul C. + + + +Author + +Freebury, Colin E. + + + +Author + +Hamilton, Paul B. + + + +Author + +Saarela, Jeffery M. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8176 +8176 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8176 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8176 +1314-2828-4-8176 + + + + +Astragalus amphioxys A. Gray + + + +Materials + + +Type status: +Other material +. Occurrence: recordNumber: 276; recordedBy: +Sokoloff, Paul C. +; preparations: Silica gel collection; Taxon: scientificName: Astragalusamphioxys A. Gray; kingdom: Plantae; phylum: Angiosperms; class: Eudicots; order: Fabales; family: Fabaceae; genus: Astragalus; specificEpithet: amphioxys; taxonRank: Species; scientificNameAuthorship: A. Gray; Location: continent: North America; country: +United States of America +; countryCode: USA; stateProvince: Utah; county: Wayne County; municipality: Hanksville; locality: +Mars Desert Research Station +; verbatimLocality: "Comm check" hill, 1.7 km northeast of Mars Desert Research Station, just west of Cow Dung Road; verbatimElevation: +1371 m +; verbatimLatitude: +38°25'3.15"N +; verbatimLongitude: +110°46'54.59"W +; coordinateUncertaintyInMeters: 50; Identification: identifiedBy: +Sokoloff, Paul C. +; dateIdentified: 2015; Event: verbatimEventDate: +November 22, 2014 +; habitat: Conglomerate sandstone hilltop dominated by Artemisia and Ephedra; Record Level: institutionID: CMN; collectionID: CAN 607473; collectionCode: +CAN, UTC +; basisOfRecord: Preserved Specimen + + +Type status: +Other material +. Occurrence: recordNumber: 292; recordedBy: +Sokoloff, Paul C. +; preparations: Silica gel collection; Taxon: scientificName: Astragalusamphioxys A. Gray; kingdom: Plantae; phylum: Angiosperms; class: Eudicots; order: Fabales; family: Fabaceae; genus: Astragalus; specificEpithet: amphioxys; taxonRank: Species; scientificNameAuthorship: A. Gray; Location: continent: North America; country: +United States of America +; countryCode: USA; stateProvince: Utah; county: Wayne County; municipality: Hanksville; locality: +Mars Desert Research Station +; verbatimLocality: Approx. 200 m past fork on Cow Dung Road, down eastern fork, 1.9 km northeast of Mars Desert Research Station; verbatimElevation: +1381 m +; verbatimLatitude: +38°25'3.2"N +; verbatimLongitude: +110°46'29.7"W +; coordinateUncertaintyInMeters: 50; Identification: identifiedBy: +Sokoloff, Paul C. +; dateIdentified: 2015; Event: verbatimEventDate: +November 23, 2014 +; habitat: Artemisia-dominated desert scrub; Record Level: institutionID: CMN; collectionID: CAN 607474; collectionCode: +CAN, UTC +; basisOfRecord: Preserved Specimen + + + + +Notes + +This species was common on sandy soil in +Atriplex-Ephedra +communities due north of MDRS (Fig. 35). +Harris (1983) +reported two varieties of this species from the nearby San Rafael Swell: +Astragalus amphioxys var. amphioxys +and +Astragalus amphioxys var. vespertinus +(E. Sheld.) M.E. Jones. Both varieties are recognized in +Barneby (1964) +and +Welsh (2006) +, which follow a nearly identical taxonomy, however we were unable to determine these collections to variety as the plants were neither flowering nor fruiting. + +Supplemental Files: CAN 607473 (Suppl. material 48), CAN 607474 (Suppl. material 49). + + + \ No newline at end of file diff --git a/data/38/95/54/389554A8757F10ABCD43C47AC9549086.xml b/data/38/95/54/389554A8757F10ABCD43C47AC9549086.xml new file mode 100644 index 00000000000..ddf9b207d4e --- /dev/null +++ b/data/38/95/54/389554A8757F10ABCD43C47AC9549086.xml @@ -0,0 +1,94 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part L) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +610 +650 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Laserpitium prutenicum +Linnaeus + +, + +Species Plantarum +1 + +: 248. 1753 + + +. + + + +"Habitat in Borussia, Lipsiae." RCN: 1997. + + + +Lectotype +(Reduron in Jarvis & al. in +Taxon +55: 213. 2006): [icon] " + +Laserpitium daucoides +prutenicum viscoso semine + +" in Breyn, Exot. Pl. Cent.: 167, t. 84. 1678. - +Epitype +(Reduron & Spalik in Jarvis & al. in +Taxon +55: 213. 2006): Poland. +"Koenigshoehe +bei Zoppot, VIII 1861, leg. +Klinggraff 264 +" (TRN). + + + + +Current name: + +Laserpitium prutenicum +L. + +( +Apiaceae +). + + + + \ No newline at end of file diff --git a/data/38/95/8A/38958ACB433B02E6300D1B814F772EB3.xml b/data/38/95/8A/38958ACB433B02E6300D1B814F772EB3.xml new file mode 100644 index 00000000000..fb919445011 --- /dev/null +++ b/data/38/95/8A/38958ACB433B02E6300D1B814F772EB3.xml @@ -0,0 +1,182 @@ + + + +Flora Helvetica - Brassicaceae + + + +Author + +Konrad Lauber + + + +Author + +Gerhart Wagner + + + +Author + +Andreas Gygax + +text + + +2018 +Haupt Verlag + +Bern + + + +Flora Helvetica + + + +480 +566 + + + +book chapter +978-3-258-08047-5 + + + + + +Lepidium campestre +(L.) R. Br. + + + + + +Artbeschreibung: +15-50 cm +hoch, oben verzweigt. +Staengel +kurz abstehend behaart. + +Untere +Blaetter +verkehrt-eifoermig +bis lanzettlich + +, +unregelmaessig +fiederteilig bis ungeteilt und ganzrandig, kurz gestielt, die oberen sitzend und mit spitzen Zipfeln umfassend, bis +4 cm +lang und +1 cm +breit. + +Kronblaetter +weiss + +, +2-3 mm +lang. +Schoetchen +flach oder +beckenfoermig +, +4-6 mm +lang und fast ebenso breit, ringsum +gefluegelt +und vorn ausgerandet. Fruchtstiele behaart. + + + + +Bluetezeit +: 4-6 + + +Standort und Verbreitung in der Schweiz: +Aecker +, +Wegraender +, +Schuttplaetze +/ kollin-montan(-subalpin) / CH + + + + +Verbreitung global: +Europaeisch + + + + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl FfrischLichtzahl LhellSalzzeichen1
Reaktionszahl Rneutral bis basisch (pH 5.5-8.5)Temperaturzahl Twarm-kollin
+Naehrstoffzahl +N + +naehrstoffreich + +Kontinentalitaetszahl +K +subkontinental (niedrige relative Luftfeuchtigkeit, grosse Temperaturschwankungen, eher kalte Winter)
+
+
+ + +Volksname Deutscher Name: +Feld-Kresse +Nom +francais +: +Passerage des champs +Nome italiano: + +Lepidio + +campestre, +Erba storna + + + + +
+
\ No newline at end of file diff --git a/data/38/95/B0/3895B09810645D6D9E14FEF8825BA6FD.xml b/data/38/95/B0/3895B09810645D6D9E14FEF8825BA6FD.xml new file mode 100644 index 00000000000..d8867d077fa --- /dev/null +++ b/data/38/95/B0/3895B09810645D6D9E14FEF8825BA6FD.xml @@ -0,0 +1,88 @@ + + + +Checklist of Georgian centipedes (Myriapoda: Chilopoda) + + + +Author + +Kiria, Eleonora +Institute of Zoology, Ilia State University, K. Cholokashvilli Ave 3 / 5, Tbilisi, Georgia +eleonora.kiria.1@iliauni.edu.ge + + + +Author + +Barjadze, Shalva +Institute of Zoology, Ilia State University, K. Cholokashvilli Ave 3 / 5, Tbilisi, Georgia + + + +Author + +Tuf, Ivan Hadrian +https://orcid.org/0000-0003-0250-0482 +Faculty of Science, Palacky University Olomouc, Slechtitelu 27, CZ- 779 00 Olomouc, Czech Republic + +text + + +Caucasiana + + +2023 + +2023-11-13 + + +2 + + +177 +188 + + + + +http://dx.doi.org/10.3897/caucasiana.2.e108535 + +journal article +http://dx.doi.org/10.3897/caucasiana.2.e108535 +2667-9809-2-177 +006F3E468B124CFC9C786E295B7A36EB +90452B36179A5EEBBBB8670614DCB680 + + + + +56. +Strigamia cf. transsilvanica (Verhoeff, 1928) + + + +Distribution in Georgia. + +Shida Kartli +• Kvemo Ermani (41) ( +Dyachkov and Zuev 2023 +). + + + +Note. + +The range of + +S. transsilvanica + +extends to Greece on the south and to the Carpathians on the east ( +Bonato et al. 2012 +), its occurrence in the Caucasus seems therefore unlikely. The taxonomic identity of the species quoted by +Dyachkov and Zuev (2023) +should be assessed. + + + + \ No newline at end of file diff --git a/data/38/95/CF/3895CF999F94557D8F57B133555362A1.xml b/data/38/95/CF/3895CF999F94557D8F57B133555362A1.xml new file mode 100644 index 00000000000..b3defce96ac --- /dev/null +++ b/data/38/95/CF/3895CF999F94557D8F57B133555362A1.xml @@ -0,0 +1,357 @@ + + + +Taxonomic revision of Muhlenbergia (Poaceae, Chloridoideae, Cynodonteae, Muhlenbergiinae) in Central America: phylogeny and classification + + + +Author + +Peterson, Paul M. +https://orcid.org/0000-0001-9405-5528 +Department of Botany MRC- 166, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013 - 7012, USA +peterson@si.edu + + + +Author + +Herrera Arrieta, Yolanda +https://orcid.org/0000-0003-3814-6518 +Instituto Politecnico Nacional, CIIDIR Unidad-Durango-COFAA, Durango, C. P. 34220, Mexico + + + +Author + +Lobo Cabezas, Silvia +https://orcid.org/0009-0007-8100-2559 +Herbario Nacional, Museo Nacional de Costa Rica, Apartado Postal 749 - 1000, San Jose, Costa Rica + + + +Author + +Romaschenko, Konstantin +https://orcid.org/0000-0002-7248-4193 +Department of Botany MRC- 166, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013 - 7012, USA + +text + + +PhytoKeys + + +2023 + +2023-08-03 + + +230 + + +1 +106 + + + + +http://dx.doi.org/10.3897/phytokeys.230.103882 + +journal article +http://dx.doi.org/10.3897/phytokeys.230.103882 +1314-2003-230-1 +365B97AE96F45DB295043BF02F4AF4BE + + + + +31. + +Muhlenbergia spiciformis Trin., +Mem +. Acad. Imp. Sci. +Saint-Petersbourg +. +Ser +. 6, Sci. Math., Seconde Pt. Sci. Nat. 6,4(3-4): 288. 1841. (Fig. 14, E-I). + + + + + +Fig. 21A-E + + + + += Muhlenbergia acutijolia +E. Fourn., Mexic. PI. 2:86. 1886. Type: +Mexico +, Veracruz, Orizaba, 8 Nov 1866,M. Bourgeau 3327 (holotype: P!; isotypes: MO-2974301!, US-87235! fragm! US-2561240!). + + += Muhlenbergia parviglumis +Vasey, Contr. U.S. Natl. Herb. 3(1):71. 1892. Type: U.S.A., Texas, 1887, +G.C. Nealley s.n. +(holotype: US-81638!; isotype: US-994967!). + + + + +Type +. + + + + +Mexico + +, "Southern + +Mexico +," + +Karwinsky s.n. +( +lectotype +: W-0002567! designated by +Peterson et al. 2007b +in +J. Bot. Res. Inst. Texas +1(2): 989; isolectotype: LE fragm!) + +. + + + +Description. + +Caespitose +perennials +, often short-lived and appearing as annuals. +Culms +25-80 cm tall, erect, slender and wiry, freely branching at the base, strigose to glabrous below the nodes; +internodes +mostly glabrous, usually 4-8 nodes per culm. +Leaf sheaths +3.5-12 cm long, shorter than the internodes, scaberulous; +ligules +1-3 mm long, deeply lacerate, margins hyaline, apex acuminate; +blades +2-12 cm long, 1-3 mm wide, flat to involute, hirsutulous to scabrous above and scaberulous below. +Panicles +4-18(-20) cm long, (0.6-)l-2.8 cm wide, narrow, contracted, sometimes interrupted below, loosely flowered; +primary branches +0.6-5 cm long, ascending and appressed occasionally spreading up to 30° from the rachises; +pedicels +0.1-3.0 mm long. +Spikelets +2.8-4 mm long, erect; +glumes +0.3-1.0 mm long, less than 1/2 as long as the lemma, 1-veined, unequal, apex obtuse to acute, sometimes erose; lower glumes shorter than the upper glumes; +lemmas +2.8-4 mm long, narrowly lanceolate, awned, purplish, scabrous roughened, sparsely appressed-pubescent on the calluses and lower 1/4 of the midveins and margins, the hairs less than 0.3 mm long, apex acuminate, the awn (10-)20-40 mm long, straight to flexuous; +paleas +2.6-3.9 mm long, narrowly lanceolate, sparsely pubescent between the veins on the basal 1/3, apex acuminate, scabrous; +anthers +0.9-1.6 mm long, purplish. +Caryopses +2-2.6 mm long, fusiform, brownish. 2 +n += 40. + + + +Distribution. + +This species ranges from the southwestern United States south to +Mexico +(Chiapas, Chihuahua, Coahuila, Hidalgo, Nuevo +Leon +, Oaxaca, Puebla, Queretaro, San Luis +Potosi +, Tamaulipas, Tlaxcala, Veracruz) [ +Peterson et al. 2007b +; +Sanchez-Ken 2018 +)]. + + + +Ecology. + + +Muhlenbergia spiciformis + +grows on rocky slopes, cliffs, and calcareous rock. + + +outcrops, often in thorn-scrub and open woodland communities associated with + +Quercus + +ssp., + +Pinus + +ssp., + +P. cembroides + +, + +Juniperus deppeana + +, + +Pseudotsuga menziesii + +, + +Abies + +, + +Cupressus + +, + +Agave + +, + +Ceanothus + +, + +Acacia + +, + +Salvia + +, + +Arbutus + +, + +Opuntia + +and + +Fraxinus + +; 450-2800 m. + + + +Comments. + +In addition to being morphologically similar to + +M. setarioides + +(see earlier comments under + +M. setarioides + +), + +M. spiciformis + +can be confused with + +M. microsperma + +but differs in not having cleistogamous spikelets in the axils of the lower culm branches, panicles narrow, contracted, 0.6-2.8 cm wide (1-6.5 cm wide in + +M. microsperma + +) primary branches spreading up to 30° from the rachises (primary branches spreading up to 80° from the rachises in + +M. microsperma + +), and ligules acuminate (truncate to obtuse in + +M. microsperma + +) [ +Peterson et al. 2007b +]. + + + +Muhlenbergia spiciformis + +is a member of +M. subg. Muhlenbergia +and is sister to the + +M. romaschenkoi +- +M. +Muhlenbergia tenuifolia + +pair in a recent biogeographical study based on DNA sequence analysis ( +Peterson et al. 2021 +). + + + +Specimens examined. + +Mexico. + +Chiapas: +Comitan +de +Dominguez + +: Laguna Chamula microwave station, +4 km +SW of Highway 190 between +Comitan +and Amatenango del Valle, +D.E. Breedlove & G. Davidse 54857 +(CAS, MO). +Jilotol +: +10 km +N of Jitotol near Rio Hondo, +D.E. Breedlove & G. Davidse 55151 +(CAS, MO). +La Trinitaria +: along Mexican Highway +190, 3 miles +south of La Trinitaria, +D.E. Breedlove & P.H. Raven 13235 +(DS, US). + +San Cristobal +de las Casas + +: NE edge of San Cristobal de las Casas, +D.E. Breedlove & G. Davidse 54748 +(NY, CAS, MO); Northeast edge of San +Cristobal +Las Casas, +D.E. Breedlove & G. Davidse 54722 +(CAS, MO); W edge of San Cristobal Las Casas, +D.E. Breedlove & G. Davidse 53980 +(CAS, MO, US); About +2 miles +SE of San +Cristobal +, +J.R. Reeder & C.G. Reeder 6066 +(MO); Grassy slope of Cerro San +Cristobal +, +R.M. Laughlin 1761 +(DS). + + + + \ No newline at end of file diff --git a/data/38/96/05/389605ECA6814C989C7077203FC0BAA2.xml b/data/38/96/05/389605ECA6814C989C7077203FC0BAA2.xml new file mode 100644 index 00000000000..d822080ac68 --- /dev/null +++ b/data/38/96/05/389605ECA6814C989C7077203FC0BAA2.xml @@ -0,0 +1,90 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part T) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +878 +905 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Teucrium spinosum +Linnaeus + +, + +Species Plantarum +2 + +: 566. 1753 + + +. + + + +"Habitat in Lusitania." RCN: 4152. + + + + + +Lectotype + +(Navarro & El Oualidi in +Acta Bot. Malac. +22: 193. 1997): Herb. Linn. No. 722.44, right specimen ( +LINN +) + +. + + + + +Current name: + + +Teucrium spinosum + +L. + +( +Lamiaceae +). + + + + \ No newline at end of file diff --git a/data/38/96/2C/38962C5DC0DA12DCC255EB5B6720368B.xml b/data/38/96/2C/38962C5DC0DA12DCC255EB5B6720368B.xml new file mode 100644 index 00000000000..41a811551cf --- /dev/null +++ b/data/38/96/2C/38962C5DC0DA12DCC255EB5B6720368B.xml @@ -0,0 +1,51 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Ichneumon extensor +[ +spec. nov. +] + + + +I. corpore nigro immaculato, abdomine cylindrico, pedibus rufis, tentaculis setaceis. + +Fn. svec. +986. + + + + +Habitat in +Europa. + + + + \ No newline at end of file diff --git a/data/38/96/C4/3896C4DFE046F77655C355FAB8A47E6B.xml b/data/38/96/C4/3896C4DFE046F77655C355FAB8A47E6B.xml new file mode 100644 index 00000000000..e15568d7f22 --- /dev/null +++ b/data/38/96/C4/3896C4DFE046F77655C355FAB8A47E6B.xml @@ -0,0 +1,101 @@ + + + +Targeting a portion of central European spider diversity for permanent preservation + + + +Author + +Candek, Klemen + + + +Author + +Gregoric, Matjaz + + + +Author + +Kostanjsek, Rok + + + +Author + +Frick, Holger + + + +Author + +Kropf, Christian + + + +Author + +Kuntner, Matjaz + +text + + +Biodiversity Data Journal + + +2013 + +1 + + +980 +980 + + + + +http://dx.doi.org/10.3897/BDJ.1.e980 + +journal article +http://dx.doi.org/10.3897/BDJ.1.e980 +1314-2828--980 + + + + +Tetragnatha nigrita Lendl, 1886 + + + +Materials + + +Occurrence: recordedBy: + +Kuntner, +Gregoric +, +Lokovsek + +; sex: +2 females +, +1 male +; Location: locationID: SI39; country: +Slovenia +; locality: +Primostek +; minimumElevationInMeters: 157; maximumElevationInMeters: 157; decimalLatitude: +45.6299 +; decimalLongitude: +15.2997 +; Event: eventDate: +2010-08-24 +; habitat: grassland + + + + + \ No newline at end of file diff --git a/data/38/96/D6/3896D64FF1B8154FC5ADD7E214BF4E69.xml b/data/38/96/D6/3896D64FF1B8154FC5ADD7E214BF4E69.xml new file mode 100644 index 00000000000..d285e8e27ee --- /dev/null +++ b/data/38/96/D6/3896D64FF1B8154FC5ADD7E214BF4E69.xml @@ -0,0 +1,122 @@ + + + +Genus Promalactis Meyrick (Lepidoptera, Oecophoridae) from China: Descriptions of twelve new species + + + +Author + +Du, Zhaohui + + + +Author + +Wang, Shuxia + +text + + +ZooKeys + + +2013 + +285 + + +23 +52 + + + + +http://dx.doi.org/10.3897/zookeys.285.4286 + +journal article +http://dx.doi.org/10.3897/zookeys.285.4286 +1313-2970-285-23 + + + + +Promalactis strumifera +sp. n. +Figs 112735 + + + +Type material. + +Holotype ♂ − China,Zhejiang Province: Mt. Jiulong ( +28°21'N +, +118°52'E +), 400 m, 5.VIII.2011, coll. Linlin Yang & Na Chen, genitalia slide No. DZH12050 (NKU). Paratypes − 1 ♂, same data as holotype except dated 4.VIII.2011; Zhejiang Province, Wuyanling ( +27°42'N +, +119°39'E +), Taishun County: 1 ♂, 400 m, 1.VIII.2005, coll. Yunli Xiao; 4 ♂, 680 m, 28.VII−2.VIII.2005, coll. Yunli Xiao; 2 ♂, 790 m, 2, 3.VIII.2007, coll. Qing Jin. Guangdong Province: 2 ♂, 1 ♀, Nanling ( +23°20'N +, +115°23'E +), Shaoguan City, 7−14.VII.2007, coll. Min Wang et al. Fujian Province: 9 ♂, 4 ♀, Sangang ( +27°45'N +, +117°40'E +), Mt. Wuyi, 740 m, 26, 27.VII.2008, coll. Weichun Li, Yongling Sun & Haiyan Bai. Guangxi Zhuang Autonomous Region: 3 ♀, Qinmu village, Yongfu County ( +24°59'N +, +109°59'E +), 160 m, 5.V.2008, coll. Li Zhang & Hui Zhen; 1 ♀, Hongqi Forest Farm, Shangsi County ( +22°09'N +, +107°58'E +), 260 m, 2.IV.2002, coll. Shulian Hao & Huaijun Xue; 1 ♀, Fubo Forest Farm, Pingxiang City ( +22°07'N +, +106°44'E +), 550 m, 1.VIII.2011, coll. Bingbing Hu et al., genitalia slide Nos. W05010 ♂, W05028 ♂, DZH11063 ♀, DZH12051 ♀, DZH12052 ♂ (NKU). Jiangxi Province: 1 ♂, Dayu County ( +25°23'N +, +114°22'E +), 15.VI.1976; 1 ♀, Dayu County, 14.VIII.1976; 1 ♂, Xingguo County, 19.VII.1976. Hunan Province: 1 ♂, Suoxiyu ( +29°35'N +, +110°57'E +), 17.X.1988, genitalia slide Nos. DZH12033 ♂, DZH12034 ♀(IOZ). + + + +Diagnosis. + +This species is similar to +Promalactis fascispinata +Du, Li & Wang, 2011, but can be separated by the rectangular gnathos, the dorsal lobe of the valva bifurcate distally +and +the ventral lobe with two digitate distal processes, and the juxta without spines in the male genitalia. In +Promalactis fascispinata +, the gnathos is tongue shaped, the dorsal lobe of the valva is not bifurcate and the ventral lobe has two elongate ovate distal processes, and the juxta has an ovate cluster of fine spines distally in the male genitalia. + + + +Description. +Adult (Fig. 11). Wingspan 8.0−11.5mm. Head with vertex shining white, frons shining leaden, occiput dark ochreous brown. Labial palpus with basal and second segments yellow on inner surface, ochreous brown on outer surface; third segment black, almost same length as second. Antenna with scape white; flagellum white except several distal flagellomeres dark brown on dorsal surface, dark brown on ventral surface. Thorax and tegula dark ochreous brown. Forewing ground colour ochreous brown tinged with dark ochreous brown, sometimes scattered with black scales on lower angle of cell; costal margin greyish black along basal 3/4, with a large rounded white spot at distal 1/4, slightly across middle of wing, edged with dense black scales except on anterior margin; two parallel oblique white streaks arising from dorsum, edged with dense black scales: basal streak from dorsal 1/5 to base of fold, second streak from beyond middle of dorsum to basal 1/3 of upper margin of cell, area ferrugineous between two streaks; dense black scales extending from apex along termen to tornus, forming a narrow black apical band; cilia yellow, dark greyish brown along distal part of costal margin, dark grey along distal part of dorsal margin. Hindwing and cilia grey. +Male genitalia (Fig. 27). Uncus stout, heavily sclerotized, sinuate marginally, with a heavily sclerotized, short, triangular apical process at middle; basal 2/3 open ventrally. Gnathos heavily sclerotized, rectangular, densely with warts, blunt at apex: right side concave in U shape near apex; lateral arm almost same length as gnathos, broad, nearly semicircular basally. Tegumen narrowly elongate, almost parallel laterally, branched from posterior 3/10, blunt anteriorly. Valva narrow, almost parallel dorso-ventrally; costa projected at middle, concave near apex; apex bilobed: dorsal lobe short and sclerotized, bifurcate distally, forming two thick spines, dorsal spine short, about 1/3 length of ventral spine, with a brush of setae between two spines; ventral lobe elongate, about 1.4 times length of dorsal lobe, weakly sclerotized, very narrow basally, broadened gradually, distally setose, bifurcate, forming two slender, digitate processes: dorsal process straight, ventral process slightly shorter than dorsal process, curved dorsad distally. Sacculus with basal 3/5 broad and almost parallel sided, distal 2/5 gradually narrowed to base of ventro-apical lobe of valva. Saccus slightly shorter than uncus, somewhat semi-oval. Juxta strong, rod-like, curved dorsad at basal 1/3, with a small awl-shaped process at base, apex narrowly rounded or bluntly pointed, reaching near posterior margin of tegumen; diaphragm with large sclerotized rumples dorsally, enlarged and protruded leftward. Aedeagus almost straight, basal 2/9 slender, slightly curved at 2/9; distal 7/9 broad, uniformly thick, apex pointed; cornutus absent. + +Female genitalia (Fig. 35). Apophysis anterioris stronger, about 1/3 length of apophysis posterioris. Eighth tergum sclerotized, nearly trapezoidal, convex antero-laterally, sinuate and with sparse long setae on posterior margin. Seventh abdominal segment sclerotized, laterally with a nodular process at anterior 2/5, posterior margin +serrate +, sometimes with large lateral tooth. Ostium bursae heavily sclerotized and large. Lamella postvaginalis with dorsal part broad leaf-like, posterior margin serrate and with sparse setae, produced to a sclerotized, ovate process at middle, margined with small teeth; ventral part with two lateral processes: left process with basal 1/3 narrow, distal 2/3 abruptly broadened, with ten spines of varied length; right process nearly spine-like, slightly curved at base. Lamella antevaginalis heavily sclerotized, very short, nearly band shaped, anterior and posterior margin convex at middle. Antrum very short, nearly funnel shaped. Ductus bursae curved, slightly longer than corpus bursae, membranous, posterior 3/5 thin, with discontinuous, weakly sclerotized bands, anterior 2/5 enlarged, with a weakly sclerotized, thin ring at anterior 2/5; ductus seminalis arising from anterior 2/5 of ductus bursae. Corpus bursae nearly oval, membranous, with dense granules; a small and rounded signum bearing one larger and one smaller conical spines, with a shield-like, weakly sclerotized plate at base. + + + +Distribution. +China (Fujian, Guangdong, Guangxi, Jiangxi, Zhejiang). + + +Etymology +. This specific name is derived from Latin strumifer (= nodular), referring to the lateral nodular process at anterior 2/5 of the 7th abdominal segment in the female genitalia. + + + \ No newline at end of file diff --git a/data/38/96/F3/3896F3F7C875DB1FC1FBD0FD6AF6044E.xml b/data/38/96/F3/3896F3F7C875DB1FC1FBD0FD6AF6044E.xml new file mode 100644 index 00000000000..7097cd3d136 --- /dev/null +++ b/data/38/96/F3/3896F3F7C875DB1FC1FBD0FD6AF6044E.xml @@ -0,0 +1,217 @@ + + + +Molecular and morphological differentiation between two Miocene-divergent lineages of Amazonian shrimps, with the description of a new species (Decapoda, Palaemonidae, Palaemon) + + + +Author + +Carvalho, Fabricio Lopes + + + +Author + +Magalhaes, Celio + + + +Author + +Mantelatto, Fernando Luis + +text + + +ZooKeys + + +2014 + +457 + + +79 +108 + + + + +http://dx.doi.org/10.3897/zookeys.457.6771 + +journal article +http://dx.doi.org/10.3897/zookeys.457.6771 +1313-2970-457-79 +7F730CC40DAA4C7E9DE776D15ACE8BCA +7F730CC40DAA4C7E9DE776D15ACE8BCA + + + +Taxon classification Animalia Decapoda Palaemonidae + + + +Palaemon carteri (Gordon, 1935) +Figures 5aand 6a + + + + +Palaemonetes carteri +Gordon, 1935: 324, fig. 12;- +Holthuis 1948 +: 113;- +Holthuis 1950b +: 32;- +Holthuis 1966 +: 6 [part, spec. from Rio +Tapajos];- + +Rodriguez +1980 + +: 126;- + +Rodriguez +1981 + +: 47 [in list];- + +Rodriguez +1982 + +: 390;- +Coelho and Ramos-Porto 1985 +: 408 [in table];- +Holthuis 1993 +: 8;- +Delgado et al. 1997 +: 16 [in list];- +Ramos-Porto and Coelho 1998 +: 337 [in list];- +Barros and Pimentel 2001 +: 20 [in list];- +Vieira 2003 +: 61;- + +Magalhaes +and Pereira 2007 + +: 9, 10, 12 [in list]; +Mora-Day et al. 2009 +: 196 [in list];- +Pereira et al. 2010a +: 606 [in list];- +Pereira et al. 2010b +: 84 [in list];- +Pileggi et al. 2013 +: 569 [part, material from +Amapa +and +Braganca +;? material from rio +Tapajos +basin]. + + +Palaemonetes (Palaemonetes) carteri +- +Holthuis 1950c +: 10 [in list];- +Holthuis 1952 +: 218, pl. 52, figs c-o, pl. 53, figs +a-c;- +Holthuis 1959 +: 81, text-fig. 9;- +Kensley and Walker 1982 +: 11 [part,? spec. from Rio Curua Una];- + +Lopez +and Pereira 1996 + +: 54, fig. 8;- + +Lopez +and Pereira 1998 + +: 77 [in list]; +Melo 2003 +: 382 [part, not Amazonas]. + + + +Holotype. +Guyana, upper Cuyuni River, ♂, col. GS Carter (NHM 1935.5.20.19). + + +Paratypes. +Karow Creek, 2 m NE of Penal Settlement, Mazaruni, 1 ♂; River Cuyuni, 1♀ov; Forest Swamp, upper Cuyuni, 1♂; same data as holotype, 7♂ 3♀ 1♀ov 1 juvenile (NHM 1935.5.20.20-29). + + +Other material. + +Suriname.Nickerie. Lower Naui Kreek, Southern Niew, 10♂ 10♀, col. DC Geijskes, 18 March 1971 (INPA 176). Brazil. +Amapa +. Floresta Nacional do +Amapa +, +igarape +Japim, 5♂ 5♀, col. CRM Santos and JEM Nanzelor, 27 October 2009 (MPEG 1108); Porto Grande, Floresta Nacional do +Amapa +, tributary of rio Araguari, 1♂ 4♀, col. CRM Santos, 28 October 2009 (CCDB 2755); +Macapa +, stream in the home of Sr. Marcondes, 1♂ 4♀ov, col. J Cunha, 6 March 2005 (MZUSP 17676). +Para +. Barcarena, Vila do Conde, 5♂ 2♀ 3♀ov, col. B Mascarenhas, 23 March 2002 (MPEG 739); +Belem +, Mocambo, 5♂ 5♀ov, col. FR Pimentel and R Maia, January 9 1998 (MPEG 528); +Belem +, Mocambo, Reserva Mocambo, 4♂ 6♀, col. FR Pimentel and J Dias, 18 June 1999 (MPEG 628); +Braganca +, Jequeri, +Sitio +Anacua +, 7♂ 9♀, 23 October 2002 (MPEG 787); Ilha do +Marajo +, cachoeira do Arari, 1♀, col. J Cunha and J Zuanon, 16 May 2008 (MZUSP 22753); Castanhal, 1♀ov, col. FL Carvalho et al., 14 December 2012 (CCDB 4338); Ilha de +Marajo +, cachoeira do Arari, rio Arari, +igarape +Popudas, 1♂ 1♀, col. J Cunha and J Zuanon, 17 May 2006 (MZUSP 23224); Laranjal do Jari, +igarape +Arapiranga, 2♀ 1♀ov, col. Moreira et al., 25 March 2008 (MZUSP 23225); +Melgaco +, Floresta Nacional de +Caxiuana +, 5♂ 4♀, 8 November 1999 (MPEG 717); Santa Maria do +Para +, 3 juveniles, col. FL Carvalho et al., 15 December 2012 (CCDB 4339); +Tucurui +, rio Tocantins basin, +igarape +Santos, 2♀, col. W Zuink and LCF Alvarenga, 16 September 1984 (MNRJ 23382). + + + +Diagnosis. +Mandibular palp absent. Rostrum slender, curved upward, reaching or just overreaching the tip of the scaphocerite; dorsal margin with 6 to 10 teeth; ventral margin with 3 to 7 teeth, usually 4 or more. Projection of the anterolateral margin of the first antennular segment overreaching the middle of the second segment, but not reaching, sometimes almost reaching, the dorsal distal margin of the second segment; anterolateral spine of the first antennular segment usually reaches the middle of the projection of the anterolateral margin. Appendix masculina up to 1.1 the length of the appendix interna, measured from their junction. Telson carrying 2 plumose setae between the inner distal stout setae; inner distal stout setae overreaching the distal tip of the telson. + + +Geographic distribution. + +Venezuela (Amazonas, +Bolivar +, Delta Amacuro, Monagas), Guyana, Suriname, French Guiana, Brazil (eastern Amazon: +Amapa +, +Para +). + + + +Ecological features. +Usually associated with riparian vegetation, leaf litter and similar microhabitats in lakes, streams and rivers, in areas with low flow. At least in the Amazon river basin, its occurrence is usually associated to clear water river systems. + + + \ No newline at end of file diff --git a/data/38/97/3D/38973DA24FB9371D4BCFECE49335090A.xml b/data/38/97/3D/38973DA24FB9371D4BCFECE49335090A.xml new file mode 100644 index 00000000000..47b9dc42c63 --- /dev/null +++ b/data/38/97/3D/38973DA24FB9371D4BCFECE49335090A.xml @@ -0,0 +1,61 @@ + + + +Genera of the Asian Catfish Families Sisoridae and Erethistidae (Teleostei: Siluriformes). + + + +Author + +Alfred W. Thomson + + + +Author + +Lawrence M. Page + +text + + +Zootaxa + + +2006 + +1345 + + +1 +96 + + + + +http://www.zoobank.org/urn:lsid:zoobank.org:pub:25EFA792-7DA4-4E0D-A69A-12591B8422DE + +journal article +z01345p001 +25EFA792-7DA4-4E0D-A69A-12591B8422DE + + + + +Gagata cenia (Hamilton 1822) + + + + +Pimelodus cenia Hamilton 1822 +: 174, pl. 31 (fig. 57). + +Type locality: n. Bengal rivers +. No types known. + + + + +Distribution: Indus, Mahanadi, Ganges, and Brahmaputra drainages in Pakistan, India, Bangladesh, Myanmar and possibly Nepal (Roberts & Ferraris, 1998; Mirza et al., 1999; Mirza, 2000; Rafique, 2000). It has also been reported from the Irrawaddy drainage (Vishwanath et al., 1998; Karmakar, 2000), and the Salween drainage (Chu et al., 1999). + + + \ No newline at end of file diff --git a/data/38/97/6C/38976CB3220A561B89818566A54D232A.xml b/data/38/97/6C/38976CB3220A561B89818566A54D232A.xml new file mode 100644 index 00000000000..fd81bfc7597 --- /dev/null +++ b/data/38/97/6C/38976CB3220A561B89818566A54D232A.xml @@ -0,0 +1,226 @@ + + + +Two new species of the tribe Meconematini (Orthoptera: Tettigoniidae: Meconematinae) from China and male song characters of Pseudocosmetura yaoluopingensis sp. nov. + + + +Author + +Wang, Tao +College of Life Sciences, Hebei University, Baoding 071002, China. +https://orcid.org/0000-0002-8714-2452 + + + +Author + +Shi, Fuming +College of Life Sciences, Hebei University, Baoding 071002, China. +shif_m@126.com + +text + + +Journal of Orthoptera Research + + +2020 + +29 + + +2 + + +115 +120 + + + + +http://dx.doi.org/10.3897/jor.29.49821 + +journal article +http://dx.doi.org/10.3897/jor.29.49821 +1937-2426-2-115 +B3FFE4D584B8566AB7732881071BB020 + + + + +Acosmetura longielata +sp. nov. +Fig. 1 + + + + +Type specimens. +- + + +Holotype +: CHINA • ♂, Guangdong, Ruyuan, Nanling, 15.VI.2019, leg. Tao Wang, MHU. +Paratypes +: CHINA • 2♂2♀, Guangdong, Ruyuan, Nanling, 15.VI.2019, leg. Tao Wang, MHU. + + + + +Description. +- + + +Male. +Body small. Fastigium verticis conical, narrower than antennal scape, blunt apically and grooved dorsally. Eyes faintly globular, obviously protruding forward and outward. Apical segment of maxillary palpus longer than subapical one; apex slightly swollen, truncate. + + +Pronotum long, distinctly prolonged posteriorly, reaching middle part of seventh abdominal tergite; anterior margin straight while posterior margin obtusely rounded (Fig. +1A +), metazona rather strikingly elevated (Fig. +1B +); lateral lobe longer than deep, metazona conspicuously extended ventrally, posterior margin without humeral sinus (Fig. +1B +). + +Tegmina short, completely covered by pronotum, overlapping, invisible in lateral view; hind wings absent. +All femora unarmed ventrally, genicular lobes with apices obtuse. Fore coxae with 1 short spine; tibiae with 5 spines respectively on both sides of ventral surface, tibial tympana open on both sides, ovoid. Middle tibiae with 5 inner and 6 outer spines on ventral surface. Hind tibiae with 2-3 spines on both sides of ventral surface as well as 22-26 spines on both sides of dorsal surface, bearing two pairs of ventral apical spurs and one pair of dorsal apical spurs. + +Lateral margins of ninth abdominal tergite slightly prolonged posteriorly (Fig. +1C +) and posterior margin of tenth abdominal tergite with a U-shaped concavity in the middle (Fig. +1G +); epiproct triangular, apical area blunt, fused with tenth abdominal tergite. Cerci cylindrical, basal areas somewhat robust, tapering apically; subapical areas significantly bent dorsad, apical areas with a small spine (Fig. +1G-J +). Genitalia sclerotized, not surpassing posterior margin of subgenital plate, apical area flat, tongue-shaped (Fig. +1I +). Subgenital plate faintly trapezoidal, basal half slightly broad, with a triangular concavity at base, apical area with a V-shaped concavity; styli stout and short, inserted on apical areas of lateral lobes of subgenital plate (Fig. +1H +). + + +Female. +Pronotum slightly shorter than male, posterior margin reaching middle part of second abdominal tergite; anterior margin somewhat straight while posterior margin obtusely rounded (Fig. +1D +); lateral lobe longer than deep, metazona gradually narrowing (Fig. +1E +). Lateral margins and posterior margin of eighth abdominal tergite feebly expanded posteriorly (Fig. +1L +). Tenth abdominal tergite a bit short, with a triangular concavity in the middle on posterior margin (Fig. +1K +); epiproct peltate, blunt apically. Cerci conical, apical areas subacute. Subgenital plate nearly trapezoidal, basal area broad, lateral margins and apical area somewhat expanded dorsad while posterior margin straight; approximate lateral margins with a V-shaped carina (Fig. +1F +). Ovipositor robust, apical half bent dorsad; dorsal and ventral margins smooth (Fig. +1L +). + + + + +Coloration. +- + + +Body yellowish green, green when alive. Eyes brown. Disc of pronotum with 1 broad longitudinal light brown stripe, of which lateral margins black-brown, outer margins of stripe with 1 longitudinal yellowish white stripe, not reaching posterior margin of pronotum (Fig. +1A, D +). Dorsal surface of abdomen with 1 longitudinal black brown stripe in the midline. Posterior margin of male genitalia black-brown (Fig. +1I +). Ovipositor light brown. Apices of all third segment of tarsi and claws blackish-brown and spines of hind tibiae black. + + + + +Measurements (mm). +- + +Body: ♂10.2-11.6, ♀11.4-12.9; pronotum: ♂7.5-8.6, ♀5.8-6.3; hind femora: ♂10.1-11.3, ♀11.8-13.0; ovipositor: 7.7-8.2. + + + +Specimens examined. +- + +CHINA • 1♀, Guangdong, Ruyuan, Nanling, 11.VI.2019, leg. Tao Wang, MHU • 1♀, Guangdong, Ruyuan, Nanling, 13.VI.2019, leg. Tao Wang, MHU • 1♂, Guangdong, Ruyuan, Nanling, 15.VI.2019, leg. Tao Wang, MHU • 1♀, Hunan, Yizhang, Mangshan, 31.VII.2019, leg. Yarui Xin, MHU. + + + +Distribution. +- + +China (Guangdong, Hunan). + + + +Discussion. +- + + +According to the caudal morphological characters of the male, this new species belongs to the genus + +Acosmetura + +. The differences between this new species and the known species of the genus + +Acosmetura + +are as follows: pronotum long, distinctly prolonged posteriorly, metazona rather strikingly elevated; female subgenital plate nearly trapezoidal, lateral margins and posterior margin somewhat expanded dorsad while posterior margin straight, approaching lateral margins with a V-shaped carina. + + + + +Etymology. +- + + +The name of this new species is derived from the male pronotum that is long and the metazona that is strongly elevated. In Latin, " +long +-" means long and " +elat +-" means elevated. + + + +Figure 1. + +Acosmetura longielata + +sp. nov. +: +A-B, D-E. +Pronotum: +A, D. +Dorsal view; +B, E. +Lateral view; +C, G, I, K-L. +Apex of abdomen: +C, L. +Lateral view; +G, K. +Dorsal view; +I. +Latero-dorsal view; +F, H. +Subgenital plate in ventral view; +J. +Right cercus in lateral view. +A-C +, +G-J +. Male; +D-F, K-L +. Female. Scale bars: 2 mm ( +A-B, D-E, L +); 1 mm ( +C, F-H, K +); 500 +μm +( +I-J +). + + + + + \ No newline at end of file diff --git a/data/38/97/B4/3897B4388961ABE26C7C1DCB242AAB9A.xml b/data/38/97/B4/3897B4388961ABE26C7C1DCB242AAB9A.xml new file mode 100644 index 00000000000..c7d89606860 --- /dev/null +++ b/data/38/97/B4/3897B4388961ABE26C7C1DCB242AAB9A.xml @@ -0,0 +1,69 @@ + + + +Guide to the littoral zone vascular flora of Carolina bay lakes (U. S. A.) + + + +Author + +Howell, Nathan + + + +Author + +Krings, Alexander + + + +Author + +Braham, Richard R + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +7964 +7964 + + + + +http://dx.doi.org/10.3897/BDJ.4.e7964 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e7964 +1314-2828-4-7964 + + + + +Solidago fistulosa Mill. + + + + +Solidago fistulosa +Taxon concept: [= RAB, GW, FNA, Weakley] + + + +Distribution +Bay Tree Lake (Rare): Howell BATR−64, 65 (NCSC!) +Horseshoe Lake: Buell 2266 (NCSC!) + + +Notes +Perennial herbs. Eulittoral zone; saturated peaty to sandy soils at or just below the mean annual high water mark (CPSI−CG). Aug−Nov. Fig. 124 + + + \ No newline at end of file diff --git a/data/38/97/DE/3897DEA50CF05E1C861F557A3BD604E1.xml b/data/38/97/DE/3897DEA50CF05E1C861F557A3BD604E1.xml new file mode 100644 index 00000000000..3198f01b063 --- /dev/null +++ b/data/38/97/DE/3897DEA50CF05E1C861F557A3BD604E1.xml @@ -0,0 +1,134 @@ + + + +Genus-level revision of the Alycaeidae (Gastropoda, Cyclophoroidea), with an annotated species catalogue + + + +Author + +Pall-Gergely, Barna +Plant Protection Institute, Centre for Agricultural Research, Herman Otto ut 15, Budapest, H- 1022, Hungary +https://orcid.org/0000-0002-6167-7221 +pallgergely2@gmail.com + + + +Author + +Sajan, Sheikh +Zoological Survey of India, Prani Vigyan Bhawan, M Block, New Alipore, Kolkata 700053, West Bengal, India & Wildlife Institute of India, Chandrabani, Dehradun 248 002, Uttarakhand, India +https://orcid.org/0000-0002-2785-6824 + + + +Author + +Tripathy, Basudev +Zoological Survey of India, Prani Vigyan Bhawan, M Block, New Alipore, Kolkata 700053, West Bengal, India + + + +Author + +Meng, Kaibaryer +National Zoological Museum of China, Institute of Zoology, Chinese Academy of Sciences, Beijing, China + + + +Author + +Asami, Takahiro +Department of Biology, Shinshu University, Matsumoto 390 - 8621, Japan +https://orcid.org/0000-0001-5706-0272 + + + +Author + +Ablett, Jonathan D. +Mollusca Section, Invertebrates Division, Department of Life Sciences, The Natural History Museums, London SW 7 5 BD, United Kingdom + +text + + +ZooKeys + + +2020 + +981 + + +1 +220 + + + + +http://dx.doi.org/10.3897/zookeys.981.53583 + +journal article +http://dx.doi.org/10.3897/zookeys.981.53583 +1313-2970-981-1 +5194AAC86B8A473F8A41470A60182A0B +7C44C797C4125A71BAE032A55E6FA5DC + + + + +Stomacosmethis praetextus (van Benthem Jutting, 1959) +Fig. 45A + + + + +Alycaeus praetextus +van Benthem Jutting, 1959: 78-79, pl. 1, fig. 1. + + + +Type locality. +"Batu Sangkarnear Pajakombo, Padang Highlands". + + +Material examined. +Sumatra: Batew Sangkar, Pajakumbok, leg. Dr. Meyer, 13.12.1955, SMF 186532 (4 paratypes). + + +Remarks. +Protoconch very finely granulated, matte; R1 with rather irregular ribs and somewhat weaker spiral striation; R2 very short, with alternating thicker/darker and narrower/lighter stripes, which are slightly elevated from the surface. + + +Figure 45. +Shells of + +Stomacosmethis + +Bollinger, 1918 species +A + +S. praetextus + +(van Benthem Jutting, 1959), paratype (SMF 186532) +B + +S. rimatus + +(O. Boettger, 1893), lectotype (SMF 109315) +C + +Stomacosmethis sadongensis + +(E. A. Smith, 1895), syntype (NHMUK 1893.6.7.73-76). Photographs: Barna +Pall-Gergely +, courtesy Ronald Janssen ( +A, B +), Harold Taylor ( +C +). + + + + + \ No newline at end of file diff --git a/data/38/98/97/3898975723BA539FA812E2F0E0C69A37.xml b/data/38/98/97/3898975723BA539FA812E2F0E0C69A37.xml new file mode 100644 index 00000000000..d9e86a34aea --- /dev/null +++ b/data/38/98/97/3898975723BA539FA812E2F0E0C69A37.xml @@ -0,0 +1,70 @@ + + + +A nomenclator of extant and fossil taxa of the Melanopsidae (Gastropoda, Cerithioidea) + + + +Author + +Neubauer, Thomas A. +https://orcid.org/0000-0002-1398-9941 +Geological-Paleontological Department, Natural History Museum Vienna, 1010 Vienna, Austria +thomas.neubauer@nhm-wien.ac.at + +text + + +ZooKeys + + +2016 + +2016-07-05 + + +602 + + +1 +358 + + + + +http://dx.doi.org/10.3897/zookeys.602.8136 + +journal article +http://dx.doi.org/10.3897/zookeys.602.8136 +1313-2970-602-1 +65EFA27673454AC69B78DBE7E98D6103 +FFA86D39FFE2FFF3FF8AFFEBC209FFDE +126863 + + + + + +Melanopsis +buccinoidea var. chlorotica Pallary, 1913 + + + + +Original source. + +Pallary 1913 +: 364. + + + +Type locality. + +"L'Abreuvoir +de Dar-Beida" [water trough of Dar +Beida +], southern Morocco. + + + + \ No newline at end of file diff --git a/data/38/98/E8/3898E8781DB13C9E1BF9109A3889ED3A.xml b/data/38/98/E8/3898E8781DB13C9E1BF9109A3889ED3A.xml new file mode 100644 index 00000000000..02b99ef122e --- /dev/null +++ b/data/38/98/E8/3898E8781DB13C9E1BF9109A3889ED3A.xml @@ -0,0 +1,89 @@ + + + +Taxonomy of the Leptogenysmodiglianii species group from southeast Asia (Hymenoptera, Formicidae, Ponerinae) + + + +Author + +Arimoto, Koichi + +text + + +ZooKeys + + +2017 + +651 + + +79 +106 + + + + +http://dx.doi.org/10.3897/zookeys.651.10336 + +journal article +http://dx.doi.org/10.3897/zookeys.651.10336 +1313-2970-651-79 +53DC0CBC09E741C891C827D31F3D99EE +53DC0CBC09E741C891C827D31F3D99EE + + + + +Leptogenys malayana +sp. n. +Figures 3, 13, 18A + + + +Etymology. + +The species epithet, +malayana +, refers to the fact that this species was found on Peninsular Malaysia. + + + +Type material. +Holotype. Worker, Trengganu, Malaysia, 1974, T. Clay leg. [BMNH]. Paratypes. 2 workers, same data as the holotype [BMNH]. +Detailed collecting locality of the types is unknown. For convenience, the location of this species is marked at the center of Trengganu Province, Malaysia, on the distribution map (Fig. 3). + + +Type locality. +Trengganu, Malaysia. + + +Distribution. +Malaysia: Peninsular Malaysia (Trengganu). + + +Worker. Diagnosis. +In full-face view, head almost as long as wide (CI: 98-101). Mandible curved near base, becoming straight apically. Antennal scape distinctly longer than width of head (SI: 115-121), surpassing posterior margin of head by two-fifths of its length. Clypeus with lateral lobe, with blunt angle between lateral lobe and median extension; apex of median extension truncate. Petiole in profile distinctly higher than long (LPI: 112-116), highest just anterior to posterodorsal angle; anterior face of node ventrally vertical and dorsally forming continuous curve with dorsum; dorsal face distinctly inclined anteriad. + + +Measurements +(n = 3, holotype in parentheses). HL: 1.57-1.63 (1.63), HLL: 1.16-1.21 (1.18), HLA: 0.17-0.19 (0.17), HW: 1.59-1.61 (1.60), CML: 0.23-0.24 (0.23), CI: 98-101 (98), CLI: 14-15 (14), SL: 1.83-1.95 (1.91), SI: 115-121 (120), EL: 0.36-0.38 (0.37), OI: 31 (31), PrL: 1.01-1.09 (1.09), PrH: 0.74-0.89 (0.89), PrW: 1.12-1.14 (1.14), WL: 2.57-2.78 (2.78), PeL: 0.88-0.97 (0.97), PeH: 1.02-1.10 (1.09), PeW: 0.72-0.76 (0.76), LPI: 112-116 (112), DPI: 77-82 (78). + + +Description. + +In full face view, head almost as long as wide. Mandible curved near base, becoming straight apically; subapical tooth distinct in holotype or absent in paratypes. Eye prominent, measuring one-third of head lateral margin length. Antennal scape distinctly longer than width of head, surpassing posterior margin of head by two-fifths of its length; antennomere III ca. 2.7 times as long as wide. Clypeus with lateral lobe, with blunt angle between lateral lobe and median extension; median extension short, with truncate apex. In dorsal view, pronotum shorter than wide. Metanotal groove slightly impressed. In profile, propodeal dorsum weakly convex to almost straight. Petiole in profile distinctly higher than long, highest just anterior to posterodorsal angle, with fan-shaped node; anterior face of node ventrally vertical and +dorsally +forming continuous curve with dorsum; dorsal face distinctly inclined anteriad; posterior face slightly concave dorsally and slightly convex ventrally. + +Head strongly areolate-rugose, longitudinally striate near clypeus; vertex weakly and transversally striate. Mandible distinctly striate longitudinally. Gastral segment I with scalloped depression that are irregular in size but generally large; large depressions close to each other; distance between small depressions greater than diameter of depressions; segments II smooth. +Body black, gaster slightly tinged with red; clypeus, mandible, antenna, legs and ventral half of petiole dark-red. Apical two or three segments of gaster red-brown. Scalloped depressions on gastral segment I bearing hairs. + + +Queen and male. +Unknown. + + + \ No newline at end of file diff --git a/data/38/99/13/3899136184B355FB99848EDBF8FBCF18.xml b/data/38/99/13/3899136184B355FB99848EDBF8FBCF18.xml new file mode 100644 index 00000000000..6f703345c3d --- /dev/null +++ b/data/38/99/13/3899136184B355FB99848EDBF8FBCF18.xml @@ -0,0 +1,179 @@ + + + +Annotated catalog and bibliography of the cyclocephaline scarab beetles (Coleoptera, Scarabaeidae, Dynastinae, Cyclocephalini) + + + +Author + +Moore, Matthew R. +Department of Entomology and Nematology, University of Florida, Building 1881 Natural Area Drive, Steinmetz Hall, Gainesville, FL 32611, USA +cyclocephala@gmail.com + + + +Author + +Cave, Ronald D. +Department of Entomology and Nematology, University of Florida, Indian River Research and Education Center, 2199 South Rock Road, Fort Pierce, FL 34945, USA + + + +Author + +Branham, Marc A. +Department of Entomology and Nematology, University of Florida, Building 1881 Natural Area Drive, Steinmetz Hall, Gainesville, FL 32611, USA + +text + + +ZooKeys + + +2018 + +2018-03-22 + + +745 + + +101 +378 + + + + +http://dx.doi.org/10.3897/zookeys.745.23685 + +journal article +http://dx.doi.org/10.3897/zookeys.745.23685 +1313-2970-745-101 +8785DC6BC2A244FD94B6243EB07C717F +047DFFCAFFA5F32EA97C873F4708943F +1222435 + + + + + +Cyclocephala +aequatoria +Endrodi +, 1963 + + + + + +Cyclocephala aequatoria +Endrodi +, 1963: 332 [original combination]. + + + +Types. + +Holotype ♀ at HNHM ( +Endrodi +Collection) ( + +Endrodi +1963 + +). + + + +Distribution. + +ECUADOR: +Canar +, Cotopaxi, Esmeraldas, Guayas, Los +Rios +, +Manabi +, Pichincha. GUATEMALA: Alta Verapaz, Izabal. MEXICO: Chiapas, Guerrero, Jalisco, +Michoacan +, Nayarit, Oaxaca, Veracruz. + + + +References. + +Barrera 1969 +, +Pike et al. 1976 +, +Dechambre 1982 +, + +Endrodi +1963 + +, +1964 +, +1966 +, +1985a +, +Balslev and Henderson 1987 +, + +Moron +et al. 1988 + +, +Ratcliffe 1992c +, +Thomas 1993 +, + +Lobo and +Moron +1993 + +, + +Delgado and +Castaneda +1994 + +, + +Ratcliffe and +Moron +1997 + +, +Ervik et al. 1999 +, +Navarrete-Heredia et al. 2001 +, +Pacheco-F. et al. 2008 +, +Ulmen et al. 2010 +, +Krajcik 2005 +, +2012 +, +Ratcliffe et al. 2013 +, +Deloya et al. 2014a +, +2016 +, + +Romero-Lopez +and +Moron +2017 + +. + + + + \ No newline at end of file diff --git a/data/38/99/46/389946CDDA3668A78E01AABE93CB1F79.xml b/data/38/99/46/389946CDDA3668A78E01AABE93CB1F79.xml new file mode 100644 index 00000000000..e1b7372a3c1 --- /dev/null +++ b/data/38/99/46/389946CDDA3668A78E01AABE93CB1F79.xml @@ -0,0 +1,72 @@ + + + +Guide to the Vascular Flora of the Savannas and Flatwoods of Shaken Creek Preserve and Vicinity (Pender & Onslow Counties, North Carolina, U. S. A.) + + + +Author + +Thornhill, Robert + + + +Author + +Krings, Alexander + + + +Author + +Lindbo, David + + + +Author + +Stucky, Jon + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1099 +1099 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1099 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1099 +1314-2828--1099 + + + + +Polygala brevifolia Nutt. + + + +Distribution +Wet pine savannas (SPS-T, SPS-RF, WLPS). + + +Notes + +Infrequent. +Jun-Oct +. Thornhill 712, 908 (NCSC). Specimens seen in the vicinity: Sandy Run [Hancock]: Taggart SARU 400 (WNC!). [= RAB, Weakley] + + + + \ No newline at end of file diff --git a/data/38/99/4E/38994ED78CD5993D765DF9DE962002C4.xml b/data/38/99/4E/38994ED78CD5993D765DF9DE962002C4.xml new file mode 100644 index 00000000000..3802b69ddc4 --- /dev/null +++ b/data/38/99/4E/38994ED78CD5993D765DF9DE962002C4.xml @@ -0,0 +1,58 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828--9042 + + + + +Lagarotis debitor (Thunberg, 1824) + + + + +Ichneumon debitor +Thunberg, 1824 + + +insolens +(Gravenhorst, 1829, +Tryphon +) + + + +Distribution +England + + + \ No newline at end of file diff --git a/data/38/99/C2/3899C29ED3B3DAF2DE16D561B5DE479E.xml b/data/38/99/C2/3899C29ED3B3DAF2DE16D561B5DE479E.xml new file mode 100644 index 00000000000..c79c4ecf634 --- /dev/null +++ b/data/38/99/C2/3899C29ED3B3DAF2DE16D561B5DE479E.xml @@ -0,0 +1,117 @@ + + + +Family-group names in Coleoptera (Insecta) + + + +Author + +Bouchard, Patrice + + + +Author + +Bousquet, Yves + + + +Author + +Davies, Anthony E. + + + +Author + +Alonso-Zarazaga, Miguel A. + + + +Author + +Lawrence, John F. + + + +Author + +Lyal, Chris H. C. + + + +Author + +Newton, Alfred F. + + + +Author + +Reid, Chris A. M. + + + +Author + +Schmitt, Michael + + + +Author + +Ślipinski, S. Adam + + + +Author + +Smith, Andrew B. T. + +text + + +ZooKeys + + +2011 + +88 + + +1 +972 + + + + +http://dx.doi.org/10.3897/zookeys.88.807 + +journal article +http://dx.doi.org/10.3897/zookeys.88.807 +1313-2970-88-1 + + + + +Tribe +Mecopelmini Thompson, 1992 + + + + +*Mecopelmini +Wood, 1966: 45 [stem: Mecopelm-]. Type genus: +Mecopelmus +Blackman, 1944. Comment: unavailable (Art. 13.1): proposed after 1930 without description or bibliographic reference to such a description. + + +Mecopelminae +Thompson, 1992: 873, in key [stem: Mecopelm-]. Type genus: +Mecopelmus +Blackman, 1944. + + + + \ No newline at end of file diff --git a/data/38/9A/4B/389A4B6B221F6C4EF2E27F2C49CF727C.xml b/data/38/9A/4B/389A4B6B221F6C4EF2E27F2C49CF727C.xml new file mode 100644 index 00000000000..fab810abd60 --- /dev/null +++ b/data/38/9A/4B/389A4B6B221F6C4EF2E27F2C49CF727C.xml @@ -0,0 +1,87 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Scyllaea pelagica +[ +spec. nov. +] + + + + +Scyllaea. + + +Mus. Ad. Fr. +1. +p. +56. Lepus pelagicus. + + +Osb. iter. +306. Zoopterygius. + + +Seb. mus. +1. +t. +74. +f. +7. + + + + +Habitat in +Pelagi +Fuco natante. + + + + +Corpus +oblongum, compressum, molluscum. +Os +apice +tenuiore perforato, edentulo. Dorsum +longitudinaliter +canaliculatum fossula crenata, qua Fuco affigitur qutescens. Postica corporis pars obtusa, latior. Brachia 3 +parium +: +primum {?X} sub ore, minus, rotundius +; +secundum sub medio corporis, foliaceum, oblongum, repandum +, obtusius, intus papillulis adspersum; +tertium +versus posteriora, simile primo pari. + + + + \ No newline at end of file diff --git a/data/38/9A/4F/389A4F9BD3AD0DD9D177369D6DF43B31.xml b/data/38/9A/4F/389A4F9BD3AD0DD9D177369D6DF43B31.xml new file mode 100644 index 00000000000..82fa33747c0 --- /dev/null +++ b/data/38/9A/4F/389A4F9BD3AD0DD9D177369D6DF43B31.xml @@ -0,0 +1,87 @@ + + + +Dwarfs under dinosaur legs: a new millipede of the order Callipodida (Diplopoda) from Cretaceous amber of Burma + + + +Author + +Stoev, Pavel + + + +Author + +Moritz, Leif + + + +Author + +Wesener, Thomas + +text + + +ZooKeys + + +2019 + +841 + + +79 +96 + + + + +http://dx.doi.org/10.3897/zookeys.841.34991 + +journal article +http://dx.doi.org/10.3897/zookeys.841.34991 +1313-2970-841-79 +422C768B44FA4F64B7ACA83B2C053A08 +422C768B44FA4F64B7ACA83B2C053A08 + + + + +Genus +† +Burmanopetalum +gen. nov. + + + +Type species. + +† +Burmanopetalum inexpectatum +sp. nov. + + + +Etymology. + +From +"Burma" +, the country of origin, and +"-petalum" +a frequent generic termination in +Callipodida +. Gender: neuter. + + + +Diagnosis. + +Differs from all extant genera of +Callipodida +by its minute size (less than 1 cm in length), lack of pleurotergal setae, and its spatulate telson being twice the size of the penultimate body ring. Eyes composed of five ommatidia. + + + + \ No newline at end of file diff --git a/data/38/9A/7E/389A7EDC456C529F86A24800B827867D.xml b/data/38/9A/7E/389A7EDC456C529F86A24800B827867D.xml new file mode 100644 index 00000000000..09687779fe4 --- /dev/null +++ b/data/38/9A/7E/389A7EDC456C529F86A24800B827867D.xml @@ -0,0 +1,86 @@ + + + +A contribution towards checklist of fungus gnats (Diptera, Diadocidiidae, Ditomyiidae, Bolitophilidae, Keroplatidae, Mycetophilidae) in Georgia, Transcaucasia + + + +Author + +Kurina, Olavi +https://orcid.org/0000-0002-4858-4629 +Institute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi st 5 D, 51006 Tartu, Estonia +olavi.kurina@emu.ee + +text + + +ZooKeys + + +2021 + +2021-03-26 + + +1026 + + +69 +142 + + + + +http://dx.doi.org/10.3897/zookeys.1026.63749 + +journal article +http://dx.doi.org/10.3897/zookeys.1026.63749 +1313-2970-1026-69 +05EFF10E62144368BE471AA57A2C38D7 +762AC1314DE05514BFD79A8DC8F34E2F + + + + +161. +Mycetophila bialorussica Dziedzicki, 1884 + + + +Material. + + +1♂ +, SZS-4 ( +ZFMK +) + +; +1♂ +, SJ-4; +1♂ +, SJ-8; +1♂ +, SJ-9. Total: +4♂♂ +. + + + + +Distribution in +Georgia +. + + +Samegrelo-Zemo Svanethi, Samtskhe-Javakheti +. + + + +General distribution. +Palaearctic. + + + \ No newline at end of file diff --git a/data/38/9A/B6/389AB65EDDCF760D9CACED81212C89F8.xml b/data/38/9A/B6/389AB65EDDCF760D9CACED81212C89F8.xml new file mode 100644 index 00000000000..c26a5ef1c26 --- /dev/null +++ b/data/38/9A/B6/389AB65EDDCF760D9CACED81212C89F8.xml @@ -0,0 +1,65 @@ + + + +Order Carnivora + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +532 +628 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Conepatus semistriatus +subsp. +taxinus +Thomas 1924 + + + + + +Synonyms: + +Conepatus semistriatus +subsp. +amazonica +(Tschundi 1844) + +. + + + + \ No newline at end of file diff --git a/data/38/9B/08/389B08E26B8350AA8441234D34A83A90.xml b/data/38/9B/08/389B08E26B8350AA8441234D34A83A90.xml new file mode 100644 index 00000000000..25215456aaa --- /dev/null +++ b/data/38/9B/08/389B08E26B8350AA8441234D34A83A90.xml @@ -0,0 +1,114 @@ + + + +The medicinal plants of Myanmar + + + +Author + +DeFilipps, Robert A. +Deceased + + + +Author + +Krupnick, Gary A. +https://orcid.org/0000-0002-1357-4826 +Department of Botany, National Museum of Natural History, Smithsonian Institution, PO Box 37012, MRC- 166, Washington, DC, 20013 - 7012, USA +krupnick@si.edu + +text + + +PhytoKeys + + +2018 + +2018-06-28 + + +102 + + +1 +341 + + + + +http://dx.doi.org/10.3897/phytokeys.102.24380 + +journal article +http://dx.doi.org/10.3897/phytokeys.102.24380 +1314-2003-102-1 +AA226A35FFF8FFBC37621A40C2518C67 +1306325 + + + + +Bombax ceiba L. (= Salmalia malabarica (DC.) Schott & Endl) + + + +Names. + +Myanmar +: +kadung +, +kawl-tung-peng +, +kroik +, +letpan +, +let-pau +, +mai-nio +. +English +: bombax, Indian kapok, red cottontree, red silk-cotton, silk-cottontree, simal. + + + +Range. +Tropical Asia. Widely distributed in Myanmar. + + +Uses. + +Bark +: Astringent and diuretic. +Leaf +, +Flower +: Used for diabetes. +Root +: Astringent and diuretic; considered to have tonic properties (including sometimes the young root). + + + +Notes. + +Medicinal uses of this species in India are discussed in +Jain and DeFilipps (1991) +. +Perry (1980) +discusses the uses of this species in China, Indo-China, Indonesia, and the Philippines. + + + +References. + +Nordal (1963) +, +Perry (1980) +. + + + + \ No newline at end of file diff --git a/data/38/9B/1B/389B1B2AB126545A9EEEADA2C429E17C.xml b/data/38/9B/1B/389B1B2AB126545A9EEEADA2C429E17C.xml new file mode 100644 index 00000000000..f73cdef1c4b --- /dev/null +++ b/data/38/9B/1B/389B1B2AB126545A9EEEADA2C429E17C.xml @@ -0,0 +1,329 @@ + + + +New descriptions and new records of the braconid parasitoids subfamilies Doryctinae and Rhyssalinae (Hymenoptera, Braconidae) in the fauna of South Korea + + + +Author + +Belokobylskij, Sergey A. +https://orcid.org/0000-0002-3646-3459 +Zoological Institute, Russian Academy of Sciences, St Petersburg 199034, Russia +doryctes@gmail.com + + + +Author + +Ku, Deokseo +https://orcid.org/0000-0002-6274-6479 +The Science Museum of Natural Enemies, Geochang 50147, Republic of Korea + +text + + +ZooKeys + + +2023 + +2023-01-05 + + +1138 + + +49 +88 + + + + +http://dx.doi.org/10.3897/zookeys.1138.94580 + +journal article +http://dx.doi.org/10.3897/zookeys.1138.94580 +1313-2970-1138-49 +623D6500707D47F69C5B2E601837C36C +DD546D8F7BE255548AA9E14411CBD152 + + + + +Aivalykus kseniae +sp. nov. + + + + +Figs 1 +, 2 + + + +Type material. + +Holotype +: female, "Korea (GB), Ian yeomul san [Ian-myeon, Yeomul-ri San] 39-4, Sangji-[shi], +36°32'46.9"N +, +128°07'46.6"E +, 2020.V.24-VI.12, Coll. S.S. Kim, The 5th National Ecosystem Survey" (NIBR). + + +Paratype +: 1 female, "Korea (GB), Cheonbu3-gil, Buk-myeon, Ulleung-gun, V.23-VI.7.2017 (Malaise trap), Ku Deokseo" (SMNE). + + + +Comparative diagnosis. + +This new species is similar to + +Aivalykus nitidus + +Belokobylskij & Chen, 2002 ( +Belokobylskij and Chen 2002 +), but differs by having the vertex with a distinct aciculation (very finely aciculate in + +A. nitidus + +), five carinae on the prescutellar depression (only a single median carina in + +A. nitidus + +), second medial abscissa (2-SR+M) short, recurrent vein (m-cu) weakly antefurcal, ~ 8.0 +x +longer than second medial abscissa (2-SR+M) (long, strongly antefurcal, in 1.6-2.0 +x +longer in + +A. nitidus + +), brachial cell closed weakly before recurrent vein (distinctly before it in + +A. nitidus + +), setae on the dorsal margin of the hind tibia short, 0.3-0.5 +x +as long as the maximum width of the tibia (long, 0.7-0.8 +x +as long as the width of the tibia in + +A. nitidus + +), and apical segments of antenna dark brown to black (three apical segments white in + +A. nitidus + +). + + + +Description. + +Female. +Body length 2.2-2.5 mm; fore wing length 2.0-2.2 mm; ovipositor sheath length 1.7-2.0 mm. + + + +Head +. + +Head width (dorsal view) 1.5-1.6 +x +its median length, 1.1 +x +width of mesoscutum. Head behind eye (dorsal view) weakly convex or subparallel in anterior 1/2, roundly narrowed in posterior 1/2; transverse diameter of eye 1.6-1.8 +x +length of temple. Ocelli small, arranged in equilateral triangle with base 1.1-1.2 +x +its sides. POL 1.1-1.2 +x +Od, 0.5-0.6 +x +OOL. Eye glabrous, 1.1-1.2 +x +as high as broad. Malar space 0.4-0.5 +x +height of eye, almost equal to basal width of mandible. Face width 0.9-1.0 +x +height of eye and almost equal to height of face and clypeus combined. Malar suture absent. Clypeus high, 1.0-1.2 +x +as wide as high. Clypeal suture shallow, distinct laterally and almost absent upper medially. Hypoclypeal depression round, its transverse width 0.4-0.5 +x +distance from edge of depression to eye, 0.3-0.4 +x +width of face. Occipital carina reduced below, not fused with hypostomal carina. + + + +Antenna +. + +Antenna slender, almost filiform, 18-21-segmented, weakly longer than body. Scape 1.2 +x +longer than its maximum width. First segment of flagellum not flattened, weakly curved, 3.8-4.0 +x +longer than its apical width, 0.7-0.8 +x +longer than second segment. Penultimate segment 4.0-4.5 +x +longer than wide, 0.8-0.9 +x +as long as first segment, as long as apical segment; the latter almost obtuse apically. + + + +Mesosoma +. + +Mesosoma 1.7-1.8 +x +longer than high. Neck of prothorax short. Pronotal carina distinct. Mesoscutum highly and almost perpendicularly elevated above pronotum (lateral view), ~ 1.1 +x +wider than its medial length (dorsal view). Notauli deep in anterior 1/2, shallow in posterior 1/2, anteriorly distinctly crenulate. Prescutellar depression (scutal sulcus) deep, with five complete or sometimes partly incomplete longitudinal carinae, smooth between carinae, 0.3 +x +as long as weakly convex scutellum. Subalar depression shallow, wide, distinctly obliquely striate. Precoxal sulcus very shallow and narrow, finely longitudinally aciculate or smooth, connected with prepectal carina anteriorly, running along ~ 1/2 of lower part of mesopleuron. Metanotum almost without tooth. + + + +Wings +. + +Fore wing 3.0-3.3 +x +longer than its maximum width. Radial vein (r) arising almost from middle of pterostigma. Radial (marginal) cell weakly shortened. Metacarp (1-R1) almost as long as pterostigma. First radial abscissa (r) perpendicular to pterostigma, 0.7-0.9 +x +as long as maximum width of pterostigma, 0.5-0.6 +x +as long as first radiomedial vein (2-SR). Second radial abscissa (3-SR+SR1) distinctly evenly curved, 6.6-7.3 +x +longer than first abscissa (r), 3.8-3.9 +x +longer than first radiomedial vein (2-SR). Discoidal (first discal) cell ~ 2.0 +x +longer than wide. Recurrent vein (m-cu) weakly antefurcal, 4.0-6.0 +x +longer than second abscissa of medial vein (2-SR+M), 0.6-0.7 +x +as long as first radiomedial vein (2-SR). Brachial (first subdiscal) cell narrow, gently closing apically weakly before recurrent vein (m-cu). Distance from nervulus (cu-a) to basal vein (1-M) 0.5-1.0 +x +nervulus (cu-a) length. In hind wing medial (basal) cell closed antero-distally. Recurrent vein (m-cu) absent, or sometimes present, but short and strongly desclerotised. + + + +Figure 1. + +Aivalykus kseniae + +sp. nov. (female, holotype) +A +habitus, lateral view +B +head, front view +C +head, dorsal view +D +head, lateral view +E +antenna +F +mesosoma, dorsal view +G +head and mesosoma, lateral view +H +hind leg. + + + + +Figure 2. + +Aivalykus kseniae + +sp. nov. (female, holotype) +A +wings +B +metasoma, dorsal view +C +metasoma, lateral view. + + + + +Legs +. + +Hind femur 3.8-4.0 +x +longer than wide. Hind tarsus 0.75-0.80 +x +as long as hind tibia. Hind basitarsus thickened, thicker than following segments, 0.7-0.8 +x +as long as second-fifth segments combined. Second segment 0.4 +x +as long as basitarsus, 1.1-1.3 +x +longer than fifth segments (without pretarsus). + + + +Metasoma +. + +Metasoma 0.9-1.0 +x +as long as head and mesosoma combined. First tergite without spiracular tubercles, spiracles situated on basal 1/3 of tergite, distinctly and linearly widened from base to apex. Maximum width of first tergite 1.7-2.0 +x +its minimum width, length 1.10-1.15 +x +its apical width, 1.3-1.5 +x +length of propodeum. Second tergite without sublateral oblique depressions. Suture between second and third tergites indistinct. Medial length of second and third tergites combined 1.1-1.2 +x +basal width of second tergite, 0.8 +x +their maximum width. Ovipositor sheath 0.8 +x +as long as body, 1.4-1.6 +x +longer than metasoma, 2.0-2.2 +x +longer than mesosoma, 0.8-0.9 +x +as long as fore wing. + + + +Sculpture and pubescence +. + +Vertex almost entirely aciculate; frons mainly smooth with fine aciculation posteriorly or widely and finely aciculate; temple smooth; face mainly smooth with sparse punctation, finely aciculate submedially on narrow stripes and below. Sides of pronotum mainly smooth but striate marginally. Mesoscutum distinctly and densely coriaceous, sometimes sculpture situated in irregular transverse dense striae anteriorly; with two middle and strongly convergent posteriorly longitudinal carina in posterior 1/2. Scutellum almost entirely smooth. but finely coriaceous laterally. Mesopleuron and metapleuron mainly smooth. Propodeum mainly smooth, with coarse and short rugulosity along median carinae in basal 2/3, with distinctly delineated by carinae, short and relatively wide smooth areola in posterior 1/3 of propodeum. Hind coxa and femur smooth. First metasomal tergite with distinct, complete, and closely situated dorsal carinae, entirely densely and distinctly striate. Remaining tergites completely smooth. Hind tibia on dorsal surface with rather sparse and semi-erect pale setae, length of these setae 0.3-0.5 +x +maximum width of hind tibia. + + + +Colour +. + +Head and anterior 1/2 of mesosoma pale reddish brown to yellowish brown; posterior 1/2 of mesosoma and first metasomal tergite dark brown to black, remaining part of metasoma reddish brown with yellowish margins. Antenna dark brown to black (including subapical and apical segments), three basal segments yellowish brown. Palpi pale yellow. Legs brownish yellow or yellow. Ovipositor sheath black. Wings faintly infuscate; pterostigma brown, but pale yellow in its basal quarter. + + +Male. +Unknown. + + + +Etymology. +Named after the daughter of the first author, Ksenia. + + +Distribution. +Korean Peninsula. + + + \ No newline at end of file diff --git a/data/38/9B/22/389B22079F0A5AE4A23B9CE1D26A3029.xml b/data/38/9B/22/389B22079F0A5AE4A23B9CE1D26A3029.xml new file mode 100644 index 00000000000..8ed54f0fa0c --- /dev/null +++ b/data/38/9B/22/389B22079F0A5AE4A23B9CE1D26A3029.xml @@ -0,0 +1,285 @@ + + + +Morphological investigation of genital organs and first insights into the phylogeny of the genus Siciliaria Vest, 1867 as a basis for a taxonomic revision (Mollusca, Gastropoda, Clausiliidae) + + + +Author + +De Mattia, Willy +https://orcid.org/0000-0002-0056-467X +Central Research Laboratories, of Natural History Museum Vienna, Burgring 7, 1010 Vienna, Austria +willy.demattia@icgeb.org + + + +Author + +Reier, Susanne +Central Research Laboratories, of Natural History Museum Vienna, Burgring 7, 1010 Vienna, Austria + + + +Author + +Haring, Elisabeth +Central Research Laboratories, of Natural History Museum Vienna, Burgring 7, 1010 Vienna, Austria + +text + + +ZooKeys + + +2021 + +2021-12-14 + + +1077 + + +1 +175 + + + + +http://dx.doi.org/10.3897/zookeys.1077.67081 + +journal article +http://dx.doi.org/10.3897/zookeys.1077.67081 +1313-2970-1077-1 +C28AD65A76F242CFBED7DFB3702CABCE +734088641608531C8E2CC69397B000ED + + + + + +Siciliaria grohmanniana grohmanniana ( +Rossmaessler +, 1836) + + + + + +Figs 1.F, 7.1-7.3, 8.1-8.4, 13.1-13.4 + + + + +Clausilia grohmanniana +Rossmaessler +1836: 7. + + +Clausilia grohmanniana var. minor +A. +Schmidt 1868 +: 40 [non +Rossmaessler +]. + + +Clausilia grohmanuiana +[sic!] - +Benoit 1876 +: 151. + + +Clausilia grohmaniana +[sic!] - +Benoit 1881 +: 108. + + +Clausilia (Siciliaria) grohmanniana +- +Monterosato 1894 +: 170. + + +Delima (Siciliaria) grohmanniana +- +Wagner 1925 +: 67. + + +Siciliaria grohmanniana +- +Schileyko 2000 +: 665. + + +Charpentieria grohmanniana +- +Beckmann 2004 +: 188. + + +Siciliaria grohmanniana +- +Nordsieck 2007 +: 53. + + +Siciliaria grohmanniana +- +Welter-Schultes 2012 +: 340. + + +Siciliaria grohmanniana +- +Nordsieck 2013b +: 6. + + +Charpentieria grohmanniana +- +De Mattia 2017a +. + + + +Specimens examined. + + +Italy +, +Sicily +, +Palermo +, +Monte Pellegrino, N +side of the top plateau, + +380 m +asl + +, +38°10'55.26"N +, +13°21'1.66"E +, +W. De Mattia +and +J. Macor +leg., +20.xii.2003 +. 15 live spm, 3 dissected spm + +. + +Italy +, +Sicily +, +Palermo +, +Monte Pellegrino +, +Santuario Santa Rosalia +, + +420 m +asl + +, +38°10'4.41"N +, +13°21'2.60"E +, [ +Lab ID +42_1, COI: +MW758886 +; +Lab ID +42_2, COI: +MW758887 +, ITS2: +MW757091MW757092 +; +Lab ID +42_3, COI: +MW758885 +], +W. De Mattia +and +J. Macor +leg., +15.iv.2017 +. 12 live spm, 3 dissected spm + +. + + + + +Shell (Figs +8 +.1-8.4, 13.1-13.4). + + +Shell mostly decollate; whorls ribbed; dorsal keel indistinct or missing; inferior lamella very high; two anterior upper palatal plicae present, upper one mostly separated from upper palatal plica; palatal edge of clausilium plate distally receding, plate gutter-like narrowed, palatal edge against distal end bent upwards and more or less pointed (as in +Nordsieck 2013b +). + + + +Measurements + +(n = 25, decollate): shell height 19.4 ++/- +0.8, whorl width 5.1 ++/- +0.2, aperture height 3.9 ++/- +0.2, aperture width 2.7 ++/- +0.2. + + + + +External morphology of the genital organs (Fig. +7 +.1). + +The FO is longer than the V (FO/V range from 1.6 to 1.8). The VD is thin along its whole course. The FDBC is shorter than the BC+SDBC (FDBC/BC+SDBC range from 0.7 to 0.8). The BC+SDBC is cylindrical or club-like and slightly longer than the V (BC+SDBC/V range 1.3-1.4), with no clear distinction between the SDBC and the BC. The apex is wide and round or pointed. The D is longer than the V (D/V range 2.0-2.1) and longer that the BC+SDBC (D/BC+SDBC range 1.4-1.7), thinner than the BC+SDBC and with a pointed apex. The V is short and cylindrical. The A is large. The PC is longer than the V (P+E/V range 2.4-2.6). The PR is long and robust. There is a clear distinction between P and E as there is a visible ER and a proximal narrowing. The E is thinner but longer than the P (E/P range 1.1-1.3), almost gradually shrinking and turning into the VD. + + + +Internal morphology of the genital organs (Figs +7 +.2, 7.3). + +The A is smooth or with weak traces of the distal penial pleats. The P presents 4-6 longitudinal and very irregular pleats. These pleats are very variable in thickness and sculpture, being both smooth or segmented along the same pleat. These pleats often split (proximally, distally or both) into smaller pleats. The fine structure of the wall is smooth. The PP is big, irregular, wrinkly and pointed. It can be smooth or with small tubercles. The P-E transition presents one ER with the PP and ELP originating from the ER. The epiphallar formula is: 1ER(PP+ELP). The E shows 4 to 6 main longitudinal finely fringed pleats. The V is almost completely smooth. The wall is finely granulated. + + +Ecology. + + +Siciliaria grohmanniana grohmanniana + +is widespread and common throughout its range. It is found to live on exposed limestone walls hiding in cracks and under crags. It is also found in + +Pinus + +sp. forest on decaying woods and tree trunks, including shady and humid spots on mosses and ferns. According to +De Mattia (2017a) + +Siciliaria grohmanniana grohmanniana + +is considered as Endangered following the IUCN criteria B1ab(i,ii,iii,v)+2ab(i,ii,iii,v). The whole area of distribution is currently included in protected areas. + + + +Distribution. +The taxon is limited to the calcareous mountains northern of Palermo: Monte Pellegrino and the southern slopes of Monte Gallo. + + + \ No newline at end of file diff --git a/data/38/9B/58/389B5826431D5C30BC2E3A406E070957.xml b/data/38/9B/58/389B5826431D5C30BC2E3A406E070957.xml new file mode 100644 index 00000000000..35d56e7cfb3 --- /dev/null +++ b/data/38/9B/58/389B5826431D5C30BC2E3A406E070957.xml @@ -0,0 +1,111 @@ + + + +Annotated type catalogue of the Megaspiridae, Orthalicidae, and Simpulopsidae (Mollusca, Gastropoda, Orthalicoidea) in the Natural History Museum, London + + + +Author + +Breure, Abraham S. H. +Naturalis Biodiversity Center, P. O. Box 9517, Leiden, the Netherlands + + + +Author + +Ablett, Jonathan D. +Natural History Museum, Division of Higher Invertebrates, London, SW 7 5 BD, UK + +text + + +ZooKeys + + +2015 + +2015-01-12 + + +470 + + +17 +143 + + + + +http://dx.doi.org/10.3897/zookeys.470.8548 + +journal article +http://dx.doi.org/10.3897/zookeys.470.8548 +1313-2970-470-17 +0E78A6A90B82401199EED5895E7F8A9E +FFDAFF85127CFFB3AA5915611C3A767A +578680 + + + + + +Simpulopsis gomesae da Silva & +Thome +, 2006 + +Figs 25i-iii + + + + +Simpulopsis gomesae + +da Silva and +Thome +2006 + +: 191, figs 19-32. + + + +Type locality. + +"Brasil, Rio Grande do Sul, +Sao +Francisco de Paula". + + + +Label. +No locality. + + +Dimensions. +Not given (range H 1.60-10.96, D 1.55-8.63 mm). Figured specimen H 6.46, D 6.93, W 3.5. + + +Type material. + +NHMUK 20050238, one paratype in ethanol, J.W. +Thome +leg. + + + +Remarks. +This taxon was based on 17 specimens; the specimen present in NHMUK was mentioned in the original paper. Its systematic position may, however, need to be critically re-examined as many taxa have already been described from this region. + + +Current systematic position. + +Simpulopsidae +, +Simpulopsis (Simpulopsis) gomesae +da Silva & +Thome +, 2006. + + + + \ No newline at end of file diff --git a/data/38/9B/5E/389B5EBFD7C25F3F8E8AA733ABA4D1E6.xml b/data/38/9B/5E/389B5EBFD7C25F3F8E8AA733ABA4D1E6.xml new file mode 100644 index 00000000000..f7a26a283a7 --- /dev/null +++ b/data/38/9B/5E/389B5EBFD7C25F3F8E8AA733ABA4D1E6.xml @@ -0,0 +1,177 @@ + + + +Contributions to the knowledge of water bugs in Mindoro Island, Philippines, with a species checklist of Nepomorpha and Gerromorpha (Insecta, Hemiptera, Heteroptera) + + + +Author + +Pelingen, Arthien Lovell +Ateneo de Manila University, Quezon City, Philippines +https://orcid.org/0000-0002-4869-1918 + + + +Author + +Zettel, Herbert +Natural History Museum, Vienna, Austria + + + +Author + +Pangantihon, Clister V +Ateneo de Manila University, Quezon City, Philippines + + + +Author + +Aldaba, Kyra Mari Dominique +Ateneo de Manila University, Quezon City, Philippines + + + +Author + +Fatallo, Earl Kevin +Ateneo de Manila University, Quezon City, Philippines + + + +Author + +de Leon, Jemillie Madonna +Ateneo de Manila University, Quezon City, Philippines + + + +Author + +Freitag, Hendrik +Ateneo de Manila University, Quezon City, Philippines +https://orcid.org/0000-0002-1325-0979 +hfreitag@ateneo.edu + +text + + +Biodiversity Data Journal + + +2020 + +8 + + +56883 +56883 + + + + +http://dx.doi.org/10.3897/BDJ.8.e56883 + +journal article +http://dx.doi.org/10.3897/BDJ.8.e56883 +1314-2828-8-e56883 +CC31F197C99F5AC8A918ED61E9EBDFAC + + + + +Hydrometra lineata Eschscholtz, 1822 + + + +Materials + + +Type status: +Other material +. +Occurrence: +individualCount: +1 female (ma) +; +Taxon: +scientificName: Hydrometralineata; +Location: +island: Mindoro; country: +Philippines +; municipality: Roxas; locationRemarks: HR1b; +Event: +eventDate: +01.07.2017 + + +Type status: +Other material +. +Occurrence: +individualCount: +1 female (ma) +; +Taxon: +scientificName: Hydrometralineata; +Location: +island: Mindoro; country: +Philippines +; municipality: Roxas; locationRemarks: HR3y; +Event: +eventDate: +21.06.2017 + + +Type status: +Other material +. +Occurrence: +individualCount: +2 males (ma) +; +Taxon: +scientificName: Hydrometralineata; +Location: +island: Mindoro; country: +Philippines +; municipality: Roxas; locationRemarks: TIR1b; +Event: +eventDate: +30.06.2017 + + + + +Distribution + + +Hydrometra lineata + +Eschscholtz, 1822 (see +Eschscholtz 1822 +) is widely distributed in the Philippines (see Fig. +7 +for new records), the Oriental Realm, Wallacea and New Guinea ( +Polhemus and Lansbury 1997 +, +Gapud et al. 2003 +). + + + +Taxon discussion + +For identification, refer to the key by +Gapud et al. (2003) +. All specimens examined were macropterous. + + + +Habitat +The species is often found in large stagnant water bodies and rarely seen in running waters; however, all our samples are from stream banks. + + + \ No newline at end of file diff --git a/data/38/9B/72/389B7252540EDFF4C01B2ADA3A5DB04E.xml b/data/38/9B/72/389B7252540EDFF4C01B2ADA3A5DB04E.xml new file mode 100644 index 00000000000..1137797c3b7 --- /dev/null +++ b/data/38/9B/72/389B7252540EDFF4C01B2ADA3A5DB04E.xml @@ -0,0 +1,63 @@ + + + +Species plantarum: exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas + + + +Author + +Linnaeus, Carolus + +text + +1753 +Laurentius Salvius + +Stockholm + + + +https://doi.org/10.5962/bhl.title.669 + +book +10.5281/zenodo.3931989 +3931989 + + + + +Statice armeria +, +spec. nov. + + + + +1. Statice caule nudo simplici capitato. +Hort. cliff. 115. Fl. suec. 253. Gron. virg. 150. Roy. lugdb. 194. + + +Limonium aphyllocaulon gramineum globosum. +Moris. hist. 3. p.601. s.15. t.1. f.29. + + +Caryophyllus montanus major, flore globoso. +Bauh. pin. 211. + + +β. Caryophyllus montanus minor. +Bauh. pin. 211. + + + + +Habitat in +Europae +& +Americae +septentrionalis campis. ♃ + + + + \ No newline at end of file diff --git a/data/38/9B/81/389B818ACE2FB65233EB995B9225D67D.xml b/data/38/9B/81/389B818ACE2FB65233EB995B9225D67D.xml new file mode 100644 index 00000000000..6429d3bd6e2 --- /dev/null +++ b/data/38/9B/81/389B818ACE2FB65233EB995B9225D67D.xml @@ -0,0 +1,70 @@ + + + +Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea + + + +Author + +Dale-Skey, Natalie + + + +Author + +Askew, Richard R. + + + +Author + +Noyes, John S. + + + +Author + +Livermore, Laurence + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8013 +8013 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8013 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8013 +1314-2828--8013 + + + + +Gastrancistrus oporinus Graham, 1969 + + + +Distribution +England, Ireland + + + \ No newline at end of file diff --git a/data/38/9C/4C/389C4CD72F81531D942EEF4DFC40EC80.xml b/data/38/9C/4C/389C4CD72F81531D942EEF4DFC40EC80.xml new file mode 100644 index 00000000000..035cbc3d0b7 --- /dev/null +++ b/data/38/9C/4C/389C4CD72F81531D942EEF4DFC40EC80.xml @@ -0,0 +1,92 @@ + + + +Floristic inventory and distribution characteristics of algific talus slopes in a specific area of forest biodiversity in South Korea + + + +Author + +Lee, Jong-Won +https://orcid.org/0000-0002-8687-8396 +Korea National Arboretum, Yanggu, Republic of Korea + + + +Author + +Yun, Ho-Geun +Korea National Arboretum, DMZ Forest Biological Conservation, Yanggu-gun, Republic of Korea + + + +Author + +Hwang, Tae Young +Korea National Arboretum, DMZ Forest Biological Conservation, Yanggu-gun, Republic of Korea + + + +Author + +Kim, Kyungmin +Daoneco, Sejong-si, Republic of Korea + + + +Author + +Jung, Se-Hoon +Daoneco, Sejong-si, Republic of Korea + + + +Author + +An, Jong Bin +Korea National Arboretum, DMZ Forest Biological Conservation, Yanggu-gun, Republic of Korea +ajb8825@korea.kr + +text + + +Biodiversity Data Journal + + +2023 + +2023-12-18 + + +11 + + +113952 +113952 + + + + +http://dx.doi.org/10.3897/BDJ.11.e113952 + +journal article +http://dx.doi.org/10.3897/BDJ.11.e113952 +1314-2828-11-e113952 +5B963235F71B550FA1E3BC1F0E590B10 + + + + + +Schizachyrium brevifolium (Sw.) Nees ex +Buese +, 1854 + + + + +Distribution +Tropics & Subtropics + + + \ No newline at end of file diff --git a/data/38/9C/62/389C624B842D51428C8CFDB36115E707.xml b/data/38/9C/62/389C624B842D51428C8CFDB36115E707.xml new file mode 100644 index 00000000000..6d6c027df04 --- /dev/null +++ b/data/38/9C/62/389C624B842D51428C8CFDB36115E707.xml @@ -0,0 +1,412 @@ + + + +Unexpected levels of cryptic diversity in European bees of the genus Andrena subgenus Taeniandrena (Hymenoptera, Andrenidae): implications for conservation + + + +Author + +Praz, Christophe +https://orcid.org/0000-0003-2649-3141 +University of Neucha ̂ tel, Institute of Biology, Rue Emile-Argand 11, 2000 Neucha ̂ tel, Switzerland & InfoFauna - Swiss Zoological Records Center, Avenue de Bellevaux 51, 2000 Neuchatel, Switzerland +christophe.praz@unine.ch + + + +Author + +Genoud, David +Avenue des Roses 2, 87240 Ambazac, France + + + +Author + +Vaucher, Killian +University of Neucha ̂ tel, Institute of Biology, Rue Emile-Argand 11, 2000 Neucha ̂ tel, Switzerland & InfoFauna - Swiss Zoological Records Center, Avenue de Bellevaux 51, 2000 Neuchatel, Switzerland + + + +Author + +Benon, Dimitri +University of Neucha ̂ tel, Institute of Biology, Rue Emile-Argand 11, 2000 Neucha ̂ tel, Switzerland & InfoFauna - Swiss Zoological Records Center, Avenue de Bellevaux 51, 2000 Neuchatel, Switzerland + + + +Author + +Monks, Joseph +Natural History Museum, Cromwell Road, London, UK + + + +Author + +Wood, Thomas J. +https://orcid.org/0000-0001-5653-224X +Laboratory of Zoology, University of Mons, Avenue du Champs de Mars 6, 7000 Mons, Belgium + +text + + +Journal of Hymenoptera Research + + +2022 + +2022-06-30 + + +91 + + +375 +428 + + + + +http://dx.doi.org/10.3897/jhr.91.82761 + +journal article +http://dx.doi.org/10.3897/jhr.91.82761 +1314-2607-91-375 +3A5B959985024CB7A83ECAA998B678A9 +3F1971FA0B4150AD801E63777D5EB924 + + + + +Andrena ovatula (Kirby, 1802) + + + + +Figs 10 +, 20 +, 30 +, 32 +, 34 +, 36 +, 46 + + + + +Melitta ovatula +Kirby, 1802: 149, ♂ [indicated as female], +"Barhamiae" +[Barham, Suffolk, UK]. See note below for information on the type material. + + + +Material examined. + +Type material +: + +Only +three males +are preserved in the Kirby collection (NHML). These males are probably +syntypes +, even if the original description only mentions the female (see +Perkins 1918 +and note above, under + +Andrena afzeliella + +). Both + +A. ovatula + +sensu + +Stoeckhert +(1930) + +and + +A. afzeliella + +occur in the +United Kingdom +near the type locality of + +A. ovatula + +(Fig. +7 +). We are not confident in the identification of these +three males +(see above under + +A. afzeliella + +). +For +this reason, we submitted a request to the +International Commission on Zoological Nomenclature +(case 3878) to set aside the existing male +syntypes +, allowing for the designation of a +neotype +for + +A. ovatula + +. +The +female specimen proposed to be the +neotype +has been collected in +Surrey +, some +130 km +southwest of the type locality of + +A. ovatula + +. +It +has been barcoded (specimen with number TJW0562 in Fig. +2 +) and agrees both morphologically and genetically with the species referred to as + +A. ovatula + +by the few authors who have separated + +A. albofasciata + +and + +A. ovatula + +( + +Stoeckhert +1930 + +; + +Niemelae +1949 + +; van der +Smissen 2002 +, +2010 +). +We +are not aware of other available names for this species (see note above with respect to the missing type material of + +A. barbata + +and + +A. picipes + +) + +. + + +Other material +: Barcoded material includes specimens from +Belgium +, +France +, +Germany +, +Italy +, +Portugal +, +Spain +, the +United Kingdom +; in addition, sequences from +Ireland +are available on BOLD. Examined material additionally includes specimens from +Andorra +; see full list of examined specimens in Suppl. material 2: Table S2. + + + +Distribution. + +Widespread in north-western Europe (France, England, Belgium, the Netherlands, Germany; Fig. +7 +); presence in Scandinavia unclear: + +Niemelae +(1949 + +: 119) mentions that this species has not been reported from Finland, but that he has examined specimens from southern Sweden in the collection D. Gaunitz (possibly in NHRS). Records from the Iberian Peninsula have been presented by +Wood et al. (2021) +. The eastern limit of its distribution needs to be further examined. We also examined specimens from the Atlas Mountains, Morocco, which are morphologically highly similar to European populations; the identity of these specimens should be confirmed using DNA barcodes (TJ Wood, in prep.). For this reason, no records are presented from north-western Africa until more extensive barcoding has been conducted. + + + +Pollen preferences. + +Analysis of 30 pollen loads from 20 localities strongly suggest oligolecty on +Fabaceae +, with 99.6% of pollen collected from this family (TJW, unpublished data). This taxon is particularly associated with members of the tribe +Genisteae +in Atlantic-influenced environments across Western Europe, such as + +Cytisus + +, + +Genista + +, and + +Ulex + +. This association with +Fabaceae +shrubs may explain the particular distribution of + +A. ovatula + +, which appears to be more frequent in coastal areas than in the central parts of Europe. + + + +Phenology. + +Bivoltine, first generation in Northern Europe from the end of March until the end of May, second generation from early June until early September, approximately a month earlier than + +A. afzeliella + +(Fig. +8 +; see under + +A. afzeliella + +). + + + +Note. + +The identity of + +Andrena poupillieri + +, a species that has been treated as a subspecies of + +A. ovatula + +, remains unclear because the Dours collection, presumably including all syntypes of this taxon, has been destroyed. +Warncke (1967 +: 176) treated + +A. poupillieri + +as a subspecies of + +A. ovatula + +sensu lato +restricted to Northern Africa, southern Spain and Crete according to the map presented by +Gusenleitner and Schwarz (2002 +: 1143). As far as we know, he did not designate a neotype for + +A. poupillieri + +. In 1975, he described + +A. poupillieri incana + +Warncke, 1975 from the Balearic Islands (Spain), suggesting that he then considered + +A. poupillieri + +as a valid species. The identity of + +A. poupillieri + +will remain unclear until a neotype is designated. We refrain from doing so until the diversity of the northern African species of + +Taeniandrena + +has been examined more carefully. Some specimens identified as + +A. poupillieri + +in the Benoist and Warncke collections have a dark terminal fringe, contradicting +Dours' +original description [ +"cinquieme +segment et anus garnis de poils +cendre +roux" (T5 and T6 furnished with ashen-reddish hairs)]; specimens with dark terminal fringe, including the type of + +A. lecerfi + +Benoist, 1961, are possibly conspecific with + +A. ovatula + +sensu stricto +, however +Dours' +original concept of + +A. poupillieri + +may be a distinct species. We present barcodes for three specimens possibly corresponding to +Dours' +original description, one with light terminal fringe (TJW024) and two with dark terminal fringe (2331 and 2333). Two of these three specimens form a clade, the third was only distantly related; neither was closely related to + +A. ovatula + +or to + +A. afzeliella + +. Future barcoding efforts for the + +Andrena + +fauna of north-western Africa are needed before the identity of + +A. poupillieri + +is settled through the designation of a neotype. Once this is achieved, the status of + +A. poupillieri incana + +should be examined; this taxon may be conspecific with + +A. poupillieri + +, or may represent another narrowly distributed species of + +Taeniandrena + +. + + + +Diagnosis. + +See under + +Andrena afzeliella + +(Table +1 +), and identification key below + + + + \ No newline at end of file diff --git a/data/38/9C/B9/389CB9C4620F5245AFD1A6B455DD1451.xml b/data/38/9C/B9/389CB9C4620F5245AFD1A6B455DD1451.xml new file mode 100644 index 00000000000..a8e389059d2 --- /dev/null +++ b/data/38/9C/B9/389CB9C4620F5245AFD1A6B455DD1451.xml @@ -0,0 +1,320 @@ + + + +Recircumscription and taxonomic revision of Siderasis, with comments on the systematics of subtribe Dichorisandrinae (Commelinaceae) + + + +Author + +Pellegrini, Marco O. O. +Universidade de Sao Paulo, Departamento de Botanica, Rua do Matao 277, CEP 05508 - 900, Sao Paulo, SP, Brazil & Jardim Botanico do Rio de Janeiro, Rua Pacheco Leao 915, CEP 22460 - 030, Rio de Janeiro, RJ, Brazil & Smithsonian Institution, NMNH, Department of Botany, MRC 166, P. O. Box 37012, Washington D. C. 20013 - 7012, USA + + + +Author + +Faden, Robert B. +Smithsonian Institution, NMNH, Department of Botany, MRC 166, P. O. Box 37012, Washington D. C. 20013 - 7012, USA + +text + + +PhytoKeys + + +2017 + +2017-07-13 + + +83 + + +1 +41 + + + + +http://dx.doi.org/10.3897/phytokeys.83.13490 + +journal article +http://dx.doi.org/10.3897/phytokeys.83.13490 +1314-2003-83-1 +FFA5FFACFF9FFFDFEE6A9A59FF8DC805 +1138093 + + + + + +6. +Siderasis zorzanellii M.Pell. & Faden +sp. nov. +Figs 1A +, 2 +, 3B-C +, 12 + + + + +Diagnosis +. + + +Similar to + +S. spectabilis + +due to its vining habit, distichously-alternate leaves, blades asymmetric at base, main florescence a many-branched thyrse, with alternate cincinni, flowers bisexual or staminate, zygomorphic, stamens unequal, curved upwards and sigmoid filaments. It can be differentiated from by its chartaceous and sparsely velutine leaves, inflorescences axillary in the primary branches or terminal in the secondary branches, and petals white with glabrous margins. + + + + +Type +. + + + +Brazil +. + +Espirito +Santo + +: + +Iuna + +, +Serra do Valentim +, ao lado do transecto 1, +20.4989°S +, +41.4725°W +, fl., +27 Mar 2014 +, +J.P.F. Zorzanelli +969 ( +holotype +: RB!; isotype: VIES!) + +. + + + +Description. + +Vines +ca. 0.5-3 m tall, terrestrial. +Roots +thin, fibrous, terminal tubers present, fusiform. +Rhizomes +buried deep in the ground. +Subterraneous stems +inconspicuous. +Aerial stems +twining, primary stem indefinite, densely branched, internodes elongate, 4.3-10.6 cm long, green, minutely velutine on both sides, hairs hyaline to light brown; secondary branches definite, unbranched, (6.4-8-)15-34 cm long, internodes elongate, 2-2.3 cm long, green, minutely velutine on both sides, hairs hyaline to light brown. +Leaves +distichously-alternate, evenly distributed along the secondary branches, sessile; sheaths 2-2.7 cm long, green to brown, minutely velutine, with a line of eglandular hairs opposite the leaf above, margins setose to densely setose, hairs hyaline to light brown; subpetiole 2.9-3.5 mm long to inconspicuous, C-shaped in section, canaliculate, membranous, green to dark green, minutely velutine on both sides, hairs hyaline to light brown; blades 5.1-12.7 +x +1.1-2.8 cm, linear elliptic to linear lanceolate, chartaceous, adaxially dark green to green, becoming dark brown when dry, abaxially light green to green, becoming greyish green to olive-green when dry, sparsely minutely velutine on both sides, hairs hyaline to light brown, base slightly asymmetric to asymmetric, cuneate to narrowly rounded, margins green to vinaceous, flat, glabrous, apex acuminate to caudate, straight; midvein conspicuous, impressed adaxially, prominent, obtuse abaxially, secondary veins 2-3 pairs, inconspicuous on both sides, becoming more evident when +dry +. +Synflorescence +composed of a solitary main florescence. +Main florescence (inflorescence) +a pedunculate, many-branched thyrse, with alternate cincinni, axillary in the primary branches or terminal in the secondary branches; basal bract reduced, rarely leaf-like, sessile, 1.7-2 +x +0.2-0.4 cm, green, minutely velutine on both sides, base opaque, margins minutely velutine, apex caudate, hairs hyaline; peduncle 0.9-1.2 cm long, light green to green, minutely velutine hairs hyaline; cincinni bract linear triangular, 3-15.3 +x +1.4-1.8 mm, green to brown, minutely velutine on both sides, base truncate, margin velutine, setose only at base, apex acuminate to caudate, hairs hyaline; cincinni 14-19 per thyrse, (1-)2-5-flowered, peduncles 1.2-5.3 mm long, white to pink, minutely velutine, hairs hyaline, erect in fruit; bracteoles ovate to broadly ovate, flat, 1-1.7 +x +0.8-1.3 mm, vinaceous to brown, minutely velutine, base rounded, margin hyaline, ciliate, apex hyaline, acute to obtuse, hairs hyaline. +Flowers +bisexual or staminate, zygomorphic, 0.7-0.9 cm diameter, pedicellate; pedicel 1.2-2.8 mm long, white, minutely velutine, hairs hyaline, patent and slightly elongate in fruit; floral buds 3.6-4.9 +x +2.2-4.1 mm, broadly obovoid to subglobose, white, apex truncate to rounded, green; sepals 3.6-4 +x +1.5-2.1 mm, narrowly ovate to elliptic, cymbiform, unequal, the uppermost external, broader and shorter than the others, fleshy, white, externally minutely velutine, hairs hyaline, internally glabrous, margin hyaline, glabrous to sparsely velutine, hairs hyaline, apex obtuse, green; petals 3.7-4.5 +x +2.7-3.4 mm, trullate to obovate, the lowermost narrower than the others, white, base cuneate, margin entire, glabrous, apex obtuse to rounded; stamens 6, unequal, the anterior longer than the posterior, curved upwards, filaments 1.3-4.2 mm long, sigmoid, white, anthers 0.7-0.9 +x +0.7-1 mm, anther sacs white, connectives quadrangular in the shorter stamens and rectangular in the longer, white; ovary 1.5-1.7 +x +1.1-1.2 mm, ellipsoid, white, velutine, hairs hyaline, style 2.7-3.2 mm long, curved upward at the apex, white; stigma annular-capitate, papillate, white. +Capsules +0.9-1.3 +x +0.8-1.2 cm, subglobose to globose, green, sparsely reticulate, sparsely velutine, hairs hyaline. +Seeds +3.6-3.9 +x +2.9-3.2 mm, obconic to ellipsoid, medium to dark brown, testa scrobiculate; hilum longer than +1/2 +the length of the seed; embryotega semidorsal; aril cream-colored, slightly translucent, thick. + + + +Specimens seen (paratypes). + + +BRAZIL. +Espirito +Santo + +: +Iuna +, Serra do Valentim, trilha do Sr. Aristides, +proximo +a +borda da mata, fl., 27 Jan 2012, J.P.F. Zorzanelli et al. 328 (VIES); floresta do Sr. Aristides, +proximo +a +borda da +vegetacao +, antes da primeira subida +ingreme +da trilha, fl., 15 Dec 2015, J.P.F. Zorzanelli 1391 (RB, VIES); floresta do Sr. Aristides, +proximo +ao +inicio +do zigue-zague da trilha, +20°21' 56" S +41°28' 26" W +, fr., 31 Mar 2016, J.P.F. Zorzanelli 1505 (RB, VIES). + + + +Etymology. + +The epithet honors the collector of the type specimens, +Joao +Paulo Fernandes Zorzanelli, Brazilian botanist and dear friend of the authors. JPFZ is an active and prominent collector in the state of +Espirito +Santo, with collections currently focused on Serra do Valentim, the type locality of + +S. zorzanellii + +. + + + +Distribution and habitat. + + +Siderasis zorzanellii + +is confined to the municipality of +Iuna +, +Espirito +Santo (Fig. +2 +). It occurs in the "Floresta +Ombrofila +Densa Montana" vegetation, at 1200-1350 m above the sea level, generally near disturbed sites, being less frequent in well-preserved areas. This could be related to its climbing habit and +the +need of more sunlight exposure then the rosette species of the genus. This pattern is common in other liana and vine groups, such as +Bignoniaceae +, +Malpighiaceae +, and +Sapindaceae +( +Acevedo-Rodriguez +, pers. comm.), especially evident in big families such as +Asteraceae +, where the primarily climbing genus + +Mikania + +Willd. is almost exclusively found at the edge of forests, along trails, and in disturbed areas (Oliveira 2015). + + + +Phenology. +It was found in bloom from December to March and in fruit in March. + + +Conservation status. + + +Siderasis zorzanellii + +is very narrowly distributed, with an EOO of ca. 7.779 km2 and an AOO of ca. 300 km2. The subpopulations are small, with no more than 10 mature individuals each. Unlike for the rosette species in the genus, it is still uncertain if the two climbing species reproduce vegetatively through cloning. Flowering seems to be frequent, although fruits have been collected only once. Thus, following the recommendations from +IUCN (2001) +, + +S. zorzanellii + +should be considered Critically Endangered [CR, A2abde+B1ab(iii, iv, v)+ B2ab(iii, iv, v)+C2a(ii)+D1+D2]. + + + +Affinities. + + +Siderasis zorzanellii + +is morphologically similar to + +S. spectabilis. + +Nevertheless, both species can be differentiated based on consistency of the leaf blades (chartaceous in + +S. zorzanellii +vs. + +membranous in + +S. spectabilis + +), density of their pubescence (sparsely minutely velutine +vs. +minutely velutine), position of the inflorescences (terminal in the secondary branches or axillary in the older nodes of the primary branches +vs. +exclusively terminal in the primary branches), floral morphology (flowers 0.7-0.9 cm diameter, petals white, margins glabrous +vs. +flowers 1-1.3 cm diameter, petals dark mauve to vinaceous, rarely light pink or white, margins ciliate with non-moniliform hairs), and by their disjunct distribution (southern montane +Espirito +Santo state +vs. +northern montane Rio de Janeiro state). + + + +Figure 12. + +Siderasis zorzanellii + +M.Pell. & Faden. +A +habit, showing an immature individual +B +habit, showing a mature individual spirally ascending a tree +C +detail of a secondary branch, showing distichously-alternate, asymmetric leaves +D +detail of an axillary inflorescence, in the primary branch +E +detail of a terminal inflorescence, at pre-anthesis, in a secondary branch +F +detail of a terminal inflorescence, at anthesis, in a secondary branch, showing an open male flower +G +side view of a male flower, showing the unequal and sigmoid stamens +H +side view of a post-anthesis bisexual flower, showing the bent style +I +detail of the inflorescence bearing two mature capsules +J +dorsal and ventral view of the seeds, showing the rugose testa, cleft towards the semidorsal embryotega, and the C-shaped hilum. Photographs by J.P.F. Zorzanelli. + + + + + + \ No newline at end of file diff --git a/data/38/9C/FB/389CFB32A11F5C33217AB1F7C3C6F3BC.xml b/data/38/9C/FB/389CFB32A11F5C33217AB1F7C3C6F3BC.xml new file mode 100644 index 00000000000..aaa2c39b841 --- /dev/null +++ b/data/38/9C/FB/389CFB32A11F5C33217AB1F7C3C6F3BC.xml @@ -0,0 +1,99 @@ + + + +New species of Agathodesmus Silvestri, 1910 from Australia (Diplopoda, Polydesmida, Haplodesmidae) + + + +Author + +Mesibov, Robert + +text + + +ZooKeys + + +2013 + +325 + + +33 +64 + + + + +http://dx.doi.org/10.3897/zookeys.325.5932 + +journal article +http://dx.doi.org/10.3897/zookeys.325.5932 +1313-2970-325-33 + + + + +Agathodesmus gayundah +sp. n. +Figs 3C, 3D, 8A, 8B + + + +Holotype. + +Male, Gayundah Creek, Hinchinbrook Island, Qld, +18°21'59"S +, +146°13'09"E ++/- +500 m, 10 m a.s.l., 11 November 1984, V. Davies, G. Thompson and J. Gallon, QM berlesate 664, rainforest sieved litter, QM S96029. + + + +Paratypes. + +QM: 4 males, 2 females, details as for holotype, S96035; 1 male, 2 females, 3 stadium 7 males, 1 stadium 7 female, 3 stadium 6 males, 4 stadium 6 females, 1 stadium 5 male, 1 stadium 4 male, same details but 9 November 1984, QM berlesate 663, S96033; 1 male, same details but 10 November 1984, QM berlesate 666, S96031; 2 males, 1 female, same details but QM berlesate 668, S96034; 1 male, 1 female, same details but 8 November 1984, G. Monteith, V. Davies, G. Thompson and J. Gallon, QM berlesate 667, S96032; 1 male, same details but QM berlesate 665, S96030; 3 males, same locality, 7-14 November 1984, V. Davies and J. Gallon, S96038; 3 males, 3 females, 2 stadium 7 females, 1 stadium 6 male, same locality, 7-15 November 1984, G. Monteith, G. Thompson and D. Cook, S96039; 3 males, 4 females, 2 stadium 7 males, 4 stadium 7 females, 1 stadium 6 male, 1 stadium 6 female, same locality but +18°21'36"S +, +146°13'33"E ++/- +500 m, 80 m a.s.l., 12 November 1984, G. Monteith, V. Davies, G. Thompson and J. Gallon, QM berlesate 669, S96036; 1 female, 2 stadium 7 females, same details but G. Monteith and G. Thompson, S96037. + + + +Other material. +None. + + +Diagnostic description. + +Male and female with head + 20 rings. Colour in alcohol very pale yellow. Male/female ca 10.5/10.5 mm long; ring 12 maximum diameter ca 0.9/1.1 mm, maximum width ca 1.25/1.3 mm. Metatergal tubercles in 10-12 irregular transverse rows, mainly without setae; metatergal setae short with slightly flared tips; lateralmost row of tubercles enlarged, together with more medial 1-2 rows forming wide pseudo-paranotum with 5-6 marginal tubercles (Figs 3C, 3D). Male leg 6 coxa with small, rounded, mediodistal projection. Telopodite (Figs 8A, 8B) with pp slightly flattened mediolaterally, slightly curved posteriorly; at in oblique plane (facing posterolaterally), short, narrowly triangular, curving posteriorly; dp directed laterobasally at base; mab directed basally and a little anteriorly, widening distally and divided into 2 lobes; longer anterior mab lobe medially concave with interior folds; shorter posterior mab lobe concave medially with flat, spike-like, basally directed process at medial edge; meb curving behind mab, divided at about one-third length into 2 paral +lel +processes, the shorter posteromedial process needle-like, the longer, wider anterolateral process terminating in triangular tooth. + + + +Figure 8. +Agathodesmus +spp. gonopod telopodites, not to same scale. A, B +Agathodesmus gayundah +sp. n., paratype ex QM S96039, right gonopod, posterior (A) and lateral (B) views C, D +Agathodesmus millaa +sp. n., paratype ex QM S96055, left gonopod, posterior (C) and lateral (D) views, as not shown in lateral view E +Agathodesmus quintanus +sp. n., paratype ex QM S96074, left gonopod, posterior and slightly basal view. + + + + +Distribution. +Known only from rainforest on Hinchinbrook Island, east of Cardwell in tropical north Queensland (Fig. 13A). + + +Name. +For the type locality, Gayundah Creek; noun in apposition. + + + \ No newline at end of file diff --git a/data/38/9D/52/389D52DE4A45AA6533478B1CA6F6FF57.xml b/data/38/9D/52/389D52DE4A45AA6533478B1CA6F6FF57.xml new file mode 100644 index 00000000000..dc9010b61eb --- /dev/null +++ b/data/38/9D/52/389D52DE4A45AA6533478B1CA6F6FF57.xml @@ -0,0 +1,100 @@ + + + +Reports on the results of dredging under the supervision of Alexander Agassiz, on the east coast of the United States, during the summer of 1880, by the U. S. coast survey steamer “ Blake, ” Commander J. R. Bartlett, U. S. N., commanding. + + + +Author + +Goode, G. B. + + + +Author + +Bean, T. H. + +text + + +Bulletin of the Museum of Comparative Zoology at Harvard College + + +1883 + +10 + + +5 + + +183 +226 + + + +journal article +10.5281/zenodo.28095 +3283BFE8-BAA3-437C-90F2-B33A8DF5125E + + + + +25. + +Melanostigma gelatinosum +, Gunther + +. + + + + + +Melanostirjma gelatinosum + +, +Guenther + + +, Proc. +Zooel +. Soc. London, 1881, Part 1, Jan. 4, p. 21 (genus, p. 20), PI. II. fig. A. + + + +A single greatly mutilated specimen, 103 mm. long, was obtained. + +It has since been taken by the U. S. Fish Commission, in the deep water ofF +Martha's +Vineyard. + + +This species was described from a specimen obtained, January 16, 1880, by Dr. Coppinger, of H. M. S. Steamer " Alert/' at Tilly Bay in the Straits of Magellan, in 24 fathoms. Dr. +Guenther +remarks {op. cit., p. 21), "The fish is evidently habitually living at a greater depth than that at which Dr. Coppinger happened to obtain the single specimen in his collection." This does not seem to us to be necessarily a logical conclusion, since, as is well known to those who have studied the distribution of deep-sea forms in the 'Western Atlantic, those which are found at great depths in temperate seas are shore inhabitants in seas near the poles. + + + + + + + + + + + + + + + + + + + +
Station.N. Lat.W. Long.Fathoms.Specimen
33438° 20' 30"73° 26' 40"3951 (fragments)
+
+
+
+
\ No newline at end of file diff --git a/data/38/9D/E6/389DE621EB165A8AAAABA928EACB2C33.xml b/data/38/9D/E6/389DE621EB165A8AAAABA928EACB2C33.xml new file mode 100644 index 00000000000..fc86a95ac5e --- /dev/null +++ b/data/38/9D/E6/389DE621EB165A8AAAABA928EACB2C33.xml @@ -0,0 +1,165 @@ + + + +Geographic and taxonomic notes, addenda and corrigenda on the subtribe Bembidiina Stephens, 1827 of the 2017 ' Catalogue of Palaearctic Coleoptera' (Coleoptera, Carabidae, Bembidiina) + + + +Author + +Neri, Paolo +Via Guido Rossa 21 " San Lorenzo ", 47121 Forli (FC), Italy + + + +Author + +Toledano, Luca +Museo Civico di Storia Naturale di Verona, Lungadige Porta Vittoria 9, 37129 Verona, Italy +lucatole2@libero.it + +text + + +ZooKeys + + +2021 + +2021-06-16 + + +1044 + + +563 +587 + + + + +http://dx.doi.org/10.3897/zookeys.1044.62593 + +journal article +http://dx.doi.org/10.3897/zookeys.1044.62593 +1313-2970-1044-563 +71DCAFC2B2BB475B91662BCDC83C7F07 +8787843B77CB51DEB6FCF0B8F3A09AC3 + + + + +Bembidion (Peryphus) obscurellum Motschulsky, 1845 + + + + +Bembidion (Peryphus) obscurellum turanicum +Csiki, 1928 + + +Bembidion (Peryphus) obscurellum fumipenne +Fassati, 1957 + + +Bembidion (Peryphus) obscurellum thibeticum +Fassati, 1957 + + +Bembidion (Peryphus) obscurellum insperatum +Lutshnik, 1938 + + + +Notes. + +Fassati (1957) +describes +Bembidion (Peryphus) fuscicrum thibeticum +ssp. nov. and +Bembidion (Peryphus) fuscicrum fumipenne +nat. nov.; they are distinguished from the nominotypical form only by the coloration of the elytra. +Lindroth (1963) +synonymizes the following taxa with + +B. obscurellum + +Motschulsky, 1845: + +B. fuscicrum + +Motschulsky, 1855, + +B. fuscicrum turanicum + +Csiki, 1928, + +B. fumipenne + +and + +B. thibeticum + +, the last two taxa because they are only color varieties. Kryzhanovskij et al. (1995) listed + +B. turanicum + +as a subspecies of + +B. obscurellum + +and retained + +B. fumipenne + +and + +B. thibeticum + +as varieties only; moreover +Belousov's +note (Kryzhanovskij et al. 1995: 85, note no. 158) reports that the subspecific situation of this polymorphic species is provisional. Recently, some authors (e.g., +Lorenz 2005 +; +Marggi et al. 2017 +) still list + +B. turanicum + +, + +B. fumipenne + +, and + +B. thibeticum + +as subspecies of + +B. obscurellum + +. + + +In light of our studies we maintain that the synonymies proposed by +Lindroth (1963) +were correct; moreover, our colleague Liang Hongbin (IZCAS, Beijing) confirms our opinion based on the study of hundreds of specimens from Mongolia that clearly show the variability of the species (Liang Hongbin, pers. comm.). + + +Regarding +Bembidion (Peryphus) obscurellum insperatum +Lutshnik, 1938, since its discriminating characters are not exclusive but shared by other subspecies, we evaluated the synonymy expressed in +Marggi et al. (2017) +and add to the distribution of the species the Russian Caucasus (ST), the region mentioned in the description, as already reported in Kryzhanovskij et al. (1995): Ciscaucasia, Western and Central Greater Caucasus. Current distribution: +E +: DE, NT, +ST +, SV; +A +: AF, CH, ES, IN, KA, KI, KZ, MG, TM, TR, WS, XIZ; +NAR +. + + + + \ No newline at end of file diff --git a/data/38/9E/58/389E580913313FD5E98D7EE7E908CBC4.xml b/data/38/9E/58/389E580913313FD5E98D7EE7E908CBC4.xml new file mode 100644 index 00000000000..1f64e9ddd17 --- /dev/null +++ b/data/38/9E/58/389E580913313FD5E98D7EE7E908CBC4.xml @@ -0,0 +1,110 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part B) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +343 +369 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Byssus velutina +Linnaeus + +, + +Species Plantarum +2 + +: 1168. 1753 + + +. + + + +"Habitat in Terra." RCN: 8401. + + + +Lectotype +(Newton in Spencer & al. in +Taxon +, in press): [icon] " + +Byssus tenerrima +viridis, velutum referens + +" in Dillenius, Hist. Musc.: 7, t. 1, f. 14. 1741. - Voucher: + +Herb. Dillenius ( +OXF +) + +. + + + + +Current name: + +Pogonatum aloides +(Hedw.) P. Beauv. + +( +Polytrichaceae +). + + + + +Note: +According to Druce & Vines ( +Dill. Herb. +: 215. 1907), voucher material in the Dillenian herbarium linked with the corresponding cited illustration is identifiable as the moss, + +Polytrichum aloides +Hedw. + +(syn. + +Pogonatum aloides +(Hedw.) P. Beauv. + +). + + + + \ No newline at end of file diff --git a/data/38/9E/D6/389ED61F70CB6F25B456A561A69AFA47.xml b/data/38/9E/D6/389ED61F70CB6F25B456A561A69AFA47.xml new file mode 100644 index 00000000000..70ec2516205 --- /dev/null +++ b/data/38/9E/D6/389ED61F70CB6F25B456A561A69AFA47.xml @@ -0,0 +1,64 @@ + + + +Berlese's Primitive Oribatid Mites + + + +Author + +van der Hammen, L. + +text + + +Zoologische Verhandelingen + + +1959 + +40 + + +1 +93 + + + + +http://www.repository.naturalis.nl/document/148866 + +journal article +ORI111 +0DC6B575-3CB3-41C1-A3EC-850520AE4487 + + + + +PERLOHMANNIIDAE +Grandjean, 1954 + + + + +Berlese (1916a) reckoned +Perlohmannia +among the representatives of the tribe +Lohmannini +, but Grandjean (1931) separated the genus from this tribe and thought that it were possible to include it in a new tribe +Trhypochthonini +. This opinion has been corrected by him in 1954 when the family +Perlohmanniidae +was created, and in 1958 when the family was placed in a superfamily +Perlohmannoidea +. + + +Collohmannia +Sellnick (1922) certainly does not belong to the +Perlohmanniidae +, so that for the moment the family consists of only one genus. + + + + \ No newline at end of file diff --git a/data/38/9E/DC/389EDC0ED13BC7D6F09701128AD0FBD8.xml b/data/38/9E/DC/389EDC0ED13BC7D6F09701128AD0FBD8.xml new file mode 100644 index 00000000000..9a2a30e19a6 --- /dev/null +++ b/data/38/9E/DC/389EDC0ED13BC7D6F09701128AD0FBD8.xml @@ -0,0 +1,86 @@ + + + +Chenopodiaceae + + + +Author + +Kuehn, U. + +text + + +1993 +Springer-Verlag + +Berlin, Heidelberg + + + + +Editor + +Kubitzki, K. + + + +Editor + +Rohwer, J. G. + + + +Editor + +Bittrich, V. + + +The Families and Genera of Vascular Plants 2 + + + +253 +281 + + + + +http://un.availab.le + +book chapter +3540555099 + + + + +49. +Halostachys C.Meyer ex Schrenk + + + + + + + +Halostachys C. Meyer ex Schrenk +, Bull. Cl. Phys.-Math. Acad Imp. Sci. St. Petersb. ll, 1: 361 (1843) + + +; + +Botsch., Not. Syst Leningrad 16: 84 (1954). + + + + + + +Shrub. Leaves succulent, scale-like. Flowers in groups of 3 in the axils of short, opposite, free bracts; perianth 3-lobed, fleshy, membranous in fruit; lobes connate to below the apex; stamen 1; stigmas 2. Embryo semi-annular; radicle inferior. One sp., +H. belangerianum (Moq.) Botsch. +, SW and C Asia. + + + + \ No newline at end of file diff --git a/data/38/9E/F4/389EF48EEF27B0A2E0908A196E23025B.xml b/data/38/9E/F4/389EF48EEF27B0A2E0908A196E23025B.xml new file mode 100644 index 00000000000..ed542ce1eda --- /dev/null +++ b/data/38/9E/F4/389EF48EEF27B0A2E0908A196E23025B.xml @@ -0,0 +1,67 @@ + + + +A key to Camponotus Mayr of Australia. + + + +Author + +McArthur, A. J. + +text + + +Memoirs of the American Entomological Institute + + + +Editor + +Snelling, R. R. + + + +Editor + +Fisher, B. L. + + + +Editor + +Ward, P. S. + + +2007 + +Advances in ant systematics (Hymenoptera: Formicidae): Homage to E. O. Wilson - 50 years of contributions. + + +80 + + +290 +351 + + + + +http://hdl.handle.net/10199/15375 + +journal article +21285 + + + + +Camponotus +rufonigrus Shattuck +& McArthur + + + +Worker. HW 1.1 - 1.4; HL 1.3 - 1.6; PW 0.9 - 1.2. Major worker not yet described. Minor worker. Black head contrasting with red mesonotum; propodeum with more than 10 erect setae scattered; pronotum and mesonotum evenly convex; metanotum indistinct; propodeum concave anteriorly, flat posteriorly, angle rounded, PD / D about 1.5; anterior clypeal margin evenly convex, carina conspicuous; dorsal and under surfaces of head, mesosoma, petiole, gaster and coxa with sparse long erect setae; entire body with short indistinct flat-lying short setae; tibiae and scapes lacking erect setae. + + + \ No newline at end of file diff --git a/data/38/9F/19/389F1980B074804EBF2DB6D86C244117.xml b/data/38/9F/19/389F1980B074804EBF2DB6D86C244117.xml new file mode 100644 index 00000000000..158b7edfbe6 --- /dev/null +++ b/data/38/9F/19/389F1980B074804EBF2DB6D86C244117.xml @@ -0,0 +1,125 @@ + + + +Family-group names in Coleoptera (Insecta) + + + +Author + +Bouchard, Patrice + + + +Author + +Bousquet, Yves + + + +Author + +Davies, Anthony E. + + + +Author + +Alonso-Zarazaga, Miguel A. + + + +Author + +Lawrence, John F. + + + +Author + +Lyal, Chris H. C. + + + +Author + +Newton, Alfred F. + + + +Author + +Reid, Chris A. M. + + + +Author + +Schmitt, Michael + + + +Author + +Ślipinski, S. Adam + + + +Author + +Smith, Andrew B. T. + +text + + +ZooKeys + + +2011 + +88 + + +1 +972 + + + + +http://dx.doi.org/10.3897/zookeys.88.807 + +journal article +http://dx.doi.org/10.3897/zookeys.88.807 +1313-2970-88-1 + + + + +Subfamily +Ptilininae Shuckard, 1839 + + + + +Ptilinidae +Shuckard, 1839b: 45 [stem: Ptilin-]. Type genus: +Ptilinus +Geoffroy, 1762 [placed on the Official List of Generic Names in Zoology (ICZN 1994a)]. + + +Sclerasteidae +Gistel, 1856a: 368 [stem: Sclerast-]. Type genus: +Sclerastes +Gistel, 1856 [this genus originally included +"pectinicornis" +and "costatus Gy", we here chose +Ptilinus +costatus Gyllenhal, 1827 as the type of +Sclerastes +; syn. nov. of +Ptilinus +Geoffroy, 1762]. Comment: syn. nov.; incorrect original stem formation, not in prevailing usage. + + + + \ No newline at end of file diff --git a/data/38/9F/CA/389FCA83FF44BD209F44910CEDBA39BE.xml b/data/38/9F/CA/389FCA83FF44BD209F44910CEDBA39BE.xml new file mode 100644 index 00000000000..a6888ae60fd --- /dev/null +++ b/data/38/9F/CA/389FCA83FF44BD209F44910CEDBA39BE.xml @@ -0,0 +1,116 @@ + + + +Faunistic diversity of spiders (Araneae) in Galichitsa mountain (FYR Macedonia) + + + +Author + +Deltshev, Christo + + + +Author + +Komnenov, Marjan + + + +Author + +Blagoev, Gergin + + + +Author + +Georgiev, Teodor + + + +Author + +Lazarov, Stoyan + + + +Author + +Stojkoska, Emilija + + + +Author + +Naumova, Maria + +text + + +Biodiversity Data Journal + + +2013 + +1 + + +977 +977 + + + + +http://dx.doi.org/10.3897/BDJ.1.e977 + +journal article +http://dx.doi.org/10.3897/BDJ.1.e977 +1314-2828--977 + + + + +latens +Dictyna +Araneae +Arachnida +Arthropoda +Animalia + + + + +Dictyna latens (Fabricius, 1775) + + + +Materials +Type status: Other material + +Occurrence: recordedBy: +C. Deltshev & M. Komnenov +; sex: +1 male, 3 females +; Location: country: +FYR of Macedonia +; locality: +Galichitsa Mt., Dzhafa pool +; verbatimElevation: +1650 m +; Event: eventDate: + +18-06-2008 + + + + +Distribution +Europeo-Central Asiatic. + + +Notes +First record in FYR of Macedonia. + + + \ No newline at end of file diff --git a/data/38/9F/FE/389FFEF7669CADE130E41550C2D7C7FA.xml b/data/38/9F/FE/389FFEF7669CADE130E41550C2D7C7FA.xml new file mode 100644 index 00000000000..6bab0dfd02e --- /dev/null +++ b/data/38/9F/FE/389FFEF7669CADE130E41550C2D7C7FA.xml @@ -0,0 +1,62 @@ + + + +Species plantarum: exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas + + + +Author + +Linnaeus, Carolus + +text + +1753 +Laurentius Salvius + +Stockholm + + + +https://doi.org/10.5962/bhl.title.669 + +book +10.5281/zenodo.3931989 +3931989 + + + + +Epilobium palustre +, +spec. nov. + + + + +6. Epilobium foliis oppositis lanceolatis integerrimis, petalis bifidis, caule erecto. +Fl. suec. 307. + + +Epilobium foliis linearibus. +Fl. lapp. 149. +Roy. lugdb. 251. + + +Lysimachia siliquosa glabra angustifolia. +Bauh. pin. 245. + + +β. Epilobium foliis lanceolatis, ramose florens. +Fl. lapp. 148. + + + + +Habitat in +Europae +humidiusculis. β in Alpibus. ♃ + + + + \ No newline at end of file diff --git a/data/38/A0/26/38A0267985095F2CBA0CB1F1AAD2BC61.xml b/data/38/A0/26/38A0267985095F2CBA0CB1F1AAD2BC61.xml new file mode 100644 index 00000000000..73395080b9d --- /dev/null +++ b/data/38/A0/26/38A0267985095F2CBA0CB1F1AAD2BC61.xml @@ -0,0 +1,159 @@ + + + +Mondeguina, a new genus for Apatetris mediterranella Nel & Varenne, 2012, with description of a new species from Portugal (Lepidoptera, Gelechiidae) + + + +Author + +Corley, Martin F. V. +Corresponding author: Pucketty Farm Cottage, Faringdon, Oxfordshire SN 7 8 JP, UK; martin. corley @ btinternet. com & CIBIO-InBIO, Centro de Investigacao em Biodiversidade e Recursos Geneticos, Universidade do Porto, Campus Agrario de Vairao, P- 4485 - 61 Vairao, Portugal; hiporame @ gmail. com +martin.corley@btinternet.com + + + +Author + +Rosete, Jorge +Urbanizacao Lourisol, Rua Manuel Cerqueira Nobrega, Lote 16, 2. frente, P- 3105 - 165 Lourical, Pombal, Portugal; roseteprof @ gmail. com + + + +Author + +Ferreira, Sonia +CIBIO-InBIO, Centro de Investigacao em Biodiversidade e Recursos Geneticos, Universidade do Porto, Campus Agrario de Vairao, P- 4485 - 61 Vairao, Portugal; hiporame @ gmail. com +https://orcid.org/0000-0002-6884-3966 + +text + + +Nota Lepidopterologica + + +2020 + +43 + + +151 +166 + + + + +http://dx.doi.org/10.3897/nl.43.50430 + +journal article +http://dx.doi.org/10.3897/nl.43.50430 +2367-5365-43-151 +BA17A1A4F2C442C1B2BDAD1F73F36D13 +CB43F23623D15D6EB50A20876F69F179 + + + + + +Catatinagma agenjoi ( +Gozmany +, 1954) + +comb. nov. + + + +Basionym. + + +Apatetris agenjoi + +Gozmany +, 1954. +Ann. Hist.-nat. Mus. Nat. Hung +. 5: 282. + + + +Type locality. +Spain, Murcia, Alberca. + +We have not had the opportunity to examine the unnamed ' + +Apatetris + +' from the Balkan countries, and consider it to be outside the scope of this paper. Available sequences from BOLD indicate two + +Dactylotula + +species (Table +1 +), yet all have been referred to + +D. kinkerella + +. From the photographs on BOLD, it is clear that those from the Czech Republic, France and Spain actually belong to + +D. altithermella + +(Walsingham, 1903). + + + +Notes. + +Against the background outlined above, it may be considered unwise of us to describe a new genus based on a species already placed in + +Apatetris + +. We justify our decision by pointing out that + +M. mediterranella + +should never have been described in + +Apatetris + +as the shape of the hindwings is quite different from that which defines the genus. In addition, the unusually long antennae are not mentioned for any species in the + +Apatetris + +group, indeed Staudinger ( +loc. cit +.) gave the antenna length as a little over half forewing length; forewing venation with M1 and M2 stalked appears to be unique in the + +Apatetris + +group; the absence of a signum in the female genitalia is also different from most + +Apatetris + +sensu lato +species, although according to Janse (1951), + +A. mirabella + +has no signum. In our view the two species considered in this paper, + +A. mediterranella + +and + +A. atlanticella + +have no place in + +Apatetris + +as defined by either Staudinger or Janse, nor in any of the related genera and therefore require a new genus. Genetic evidence provided by the DNA barcode fragments sequenced corroborates their distinctness from other + +Apatetris + +sensu lato +available in the BOLD database, either European or from other continents (Fig. +1 +). + + + + \ No newline at end of file diff --git a/data/38/A0/81/38A081137C40A07D4CAA15A5745775F6.xml b/data/38/A0/81/38A081137C40A07D4CAA15A5745775F6.xml new file mode 100644 index 00000000000..c63317a5a84 --- /dev/null +++ b/data/38/A0/81/38A081137C40A07D4CAA15A5745775F6.xml @@ -0,0 +1,357 @@ + + + +Order Rodentia - Family Cricetidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 2 + + + +955 +1189 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316535 + + + + + +Phaiomys +Blyth 1863 + + + + + + + +Phaiomys +Blyth 1863 + +, +J. Asiat. Soc. Bengal, 32 (1): 89 + +. + + + + +Type Species: + +Phaiomys leucurus +Blyth 1863 + + + + + +Species and subspecies: +1 species: + + +Species + +Phaiomys leucurus +Blyth 1863 + + + + + +Discussion: + +Arvicolini. Variably recognized as a genus ( +Ellerman, 1941 +; +Hinton, 1923 +, + +1926 +a + +; +R +. A. +Martin, 1987 +, + +1989 +b + +; +Repenning, 1992 +; +Repenning et al., 1990 +); a subgenus of + +Microtus + +(G. M. Allen, 1940; +Ellerman and Morrison-Scott, 1951 +; +Musser and Carleton, 1993 +; +Ognev, 1950 +); a subgenus of + +Pitymys + +( + +Corbet, 1978 +c + +; + +Ellerman, 1947 +a + +, 1961; +Zheng and Wang, 1980 +); or a subgenus of + +Neodon + +( +Gromov and Polyakov, 1977 +; +Zagorodnyuk, 1990 +, + +1992 +c + +). +Nadachowski and Zagorodnyuk (1996) +identified + +Phaiomys leucurus + +as a Pleistocene relict because its M3 and m1 occlusal patterns are simple and closely similar to the extinct + +Allophaiomys + +. +Chaline (1987:253) +proclaimed that "an isolate of the ancestral + +Allophaiomys pliocaenicus + +stayed in the Himalayas and survives as + +Phaiomys leucurus + +." +R +. A. +Martin (1987 +, + +1989 +b + +) thought the m1 patterns in + +Allophaiomys pliocaenicus + +and + +Phaiomys + +to be so similar that he included the former as subgenus of the latter, and later (1995) acknowledged the differences between the two at the species level. +Kormos (1932) +, however, who named and first described + +Allophaiomys + +, noted cranial, mandibular, and minor dental traits that contrast the two genera, and +Repenning (1992) +described other minute but significant dental differences between them. + + + +Hinton (1926 +a +:48) + +believed that + +P. leucurus + +is "closely related to + +Arvicola + +, and seems like the latter to be descended from some close ally of + +Mimomys + +. " This relationship was formalized by +Kretzoi (1955 +; also +Repenning et al., 1990 +, and +Repenning, 1992 +), who included + +Phaiomys + +, + +Arvicola + +, and + +Allophaiomys + +, all with rootless molars, in the Arvicolini (not as used here), along with + +Mimomys + +and other fossil genera that possess rooted molars and a range in hypsodonty. + +Phaiomys + +can be derived from + +Allophaiomys + +, which in turn was presumably descended "from a still inadequately identified + +Mimomys + +lineage" ( +Chaline et al., 1999 +). Both M3 and m1 occlusal patterns are also closely similar in + +Phaiomys + +and + +Arvicola + +(see + +Hinton, 1926 +a + +; +Rekovets, 1990 +); moreover, the cranium of + +Phaiomys + +is stout and rugged, with very short and posteriorly constricted incisive foramina, a conformation similar to species of + +Arvicola + +but unlike any + +Microtus + +, and in particular unlike + +Neodon + +with which + +Phaiomys + +has been associated. Repenning explicitly denied any close tie between + +Phaiomys + +and + +Neodon + +, allocating the latter to Pitymyini and thereby viewing + +Phaiomys + +and + +Neodon + +as independent lineages derived from ancestral + +Allophaiomys + +. Along with the molar differences, other external and cranial contrasts—compared with + +Neodon + +, + +Phaiomys + +has longer and stouter foreclaws, a robust and deeper cranium, much shorter and posteriorly constricted incisive foramina, inflated auditory bulla, moderately inflated mastoid region, and robust mandible with prominent alveolar processes—support a view of two genera. + + +The hypothesis that + +Phaiomys + +is a monophyletic lineage (genus) independent of the radiation of species-groups within + +Microtus + +draws attention to its morphological connection to ancestral + +Allophaiomys + +, as argued by paleontologists, and provides a taxonomic framework to explore its postulated alliance with + +Arvicola + +, other relictual groups ( + +Blanfordimys + +and + +Neodon + +), and species of + +Microtus + +using molecular analyses and a broader variety of morphological data than molar patterns. + +Phaiomys leucurus + +occurs only at high altitudes in the rugged Himalayas and Tibetan Plateau at the periphery of the Palearctic range of Arvicolini, a region +Hinton (1923:155) +emphasized as "that great refuge for archaic Microtines formed by the highlands of Central and South-eastern Asia." + +. + + + + \ No newline at end of file diff --git a/data/38/A0/9F/38A09F98578ED0ABFC166ABF0F423BE9.xml b/data/38/A0/9F/38A09F98578ED0ABFC166ABF0F423BE9.xml new file mode 100644 index 00000000000..873f59459c8 --- /dev/null +++ b/data/38/A0/9F/38A09F98578ED0ABFC166ABF0F423BE9.xml @@ -0,0 +1,200 @@ + + + +Hymenopterologische Studien. 1. Formicariae. + + + +Author + +Förster, A. + +text + +1850 +Unknown Publisher + +Aachen + + + +http://antbase.org/ants/publications/8138/8138.pdf + +book +8138 + + + + +24. +Myrm. bidens +n. sp. + + + +Operaria: Nigra, albido-pilosula, capite antice, antennis, thorace antice et postice pedibusque rufis, bis femoribus et tibiis crassis; clypeo bidentato; capite thoraceque longitudinaliter striatim rugulosis; metanoto spinis duabus parvis subhorizontalibus. Long. 1 1/3 lin. +Femina: Nigra, albido-pilosula, capite antice, antennis, thorace antice et postice pedibusque laetc rufis, femoribus tibiisque crassiusculis; clypeo evidenter bidentato; ocellis minutis; capite longitudinaliter striatim rugulosa; mesonoto sublaevi; spinis duabus metanoti parvis. Long, 1 1/2 lin. + +Diese Art ist leicht kenntlich an der +eigenthuemlichen +Bildung des Clypeus, auch durch die +Faerbung +laesst +sie sich leicht von andern Arten unterscheiden. Bei dem Arbeiter ist der Kopf etwas +verlaengert +und breiter als der Mittelleib, die +Faerbung +vorherrschend schwarz, aber vorne sowohl auf der Ober- wie auf der Unterseite mit +Einschluss +der Mandibeln und der +Fuehler +roth. An der Seile zieht sich die rothe +Faerbung +bis zu den Netzaugen hiuauf, welche klein sind und sich kaum +ueber +die +Oberflaeche +erheben. Nebenaugen fehlen +gaenzlich +. Die Mandibeln sind stark, an der Spitze erweitert und +voellig +glatt, an der Basis sehr wenig und undeutlich runzlich. Der Clypeus ist klein, nicht scharf begrenzt, nicht +gewoelbt +, sondern vielmehr etwas +eingedrueckt +mit einem nicht ganz durchgehenden Mittelkiel, ander Spitze beiderseits in einen stumpfen, aber scharf vortretenden Zahn auslaufend. Die +Fuehler +12-gliedrig, der Schaft +ungefaehr +so lang wie alle +uebrigen +Glieder zusammen genommen, mit +Ausschluss +des letzten, das 1 - 7te Glied der +Geissel +stark +verkuerzt +, daher breiter als lang, die 3 folgenden oder die Endglieder +derGeissel +stark verdickt, eine Keule bildend, das 8te und 9te +ungefaehr +gleich an +Laenge +, aber das 9te etwas dicker als das 8te; das 10te Glied der +Geissel +oder das letzte des ganzen +Fuehlers +noch viel dicker als die beiden vorhergehenden und +ungefaehr +so lang als die 4 verletzten Glieder zusammen genommen. Die Stirnlamellen nicht besonders stark entwickelt, +rothgefaerbt +, eine area frontalis nicht abgegrenzt, aber ein dreieckiger, mit der Spitze nach dem Scheitel, gerichteter Raum zwischen und etwas +ueber +den Stirnlamellen fast glatt und nicht mit +Laengsrunzeln +bedeckt. Der ganze Kopf erscheint +uebrigens +mit starken +Laengsrunzeln +bedeckt, zu welchen +seitwaerts +noch kleine Querrunzeln kommen, welche die +Oberflaeche +netzaderig erscheinen lassen. Hinter den Augen und zwar +seitwaerts +ist der Kopf +voellig +glatt und scharf gerandet. Der ganze Kopf sammt den +Fueh- +lern wird durch +weissliche +, ziemlich dichte Behaarung rauh; Am Mittelleib ist der Prothorax, die +abschuessige +Stelle des Metathorax und die ganze Unterseite mehr oder weniger dunkelroth, das Mesonotum mit starken +Laengsrunzeln +bedeckt, das Metanotum mit 2 ziemlich spitzen, aber nicht langen, sondern mehr zahnartigen Dornen bewaffnet, welche fast genau eine horizontale Lage haben; die +abschuessige +Stelle ganz glatt, +rothgefaerbt +. Die Beine ganz roth, die Schenkel und Schienen stark verdickt, namentlich letztere, alle Theile derselben wie der ganze Mittelleib stark behaart. Der Hinterleib ganz schwarz, stark borstenhaarig-, das lste Segment ganz, der Hinterrand des 2 - 4ten und die +uebrigen +wieder ganz roth; auf der Bauchseite tritt diese rothe +Faerbung +fast noch deutlicher hervor. Das 1ste Segment +verhaeltnissmaessig +kurz, weil der 1ste Knoten sehr kurz ist, die vordere Seite desselben sehr kurz und glatt, hinter derselben hat dieser Knoten eine leichte +Quereinschnuerung +, auf der Unterseite tritt ein ganz kurzer und stumpfer Kiel nur undeutlich hervor. Der hintere Knoten ist etwas +hoeher +als der vordere, auf der Unterseite nicht bewaffnet und so wie der vordere mit ziemlich starken +Laengsrunzeln +versehen. Die +uebrigen +, Segmente geben dem Hinterleib ein fast kugeliges Ansehen. Der ganze Habitus dieser Art erscheint kurz gedrungen und +kraeftiger +als bei andern Arten von derselben +Groesse +. + + +Das +ungefluegelte +Weibchen ist etwas +groesser +als der Arbeiter, in der +Faerbung +demselben vollkommen gleich, nur ist diese +ueberall +noch heller und intensiver, so wie auch +schaerfer +begraenzt, in der Sculptur zeigen sich aber einige Abweichungen. Die +Fuehler +sind ganz wie bei dem Arbeiter, nur ist der Schaft an der Basis noch etwas deutlicher winklig gebrochen, der Clypeus nach oben etwas deutlicher abgesetzt und der Mittelkiel etwas +schaerfer +, die +Zaehne +eben so scharf. Die Mandibeln 10- +zaehnig +, der +aeusserste +Zahn kurz, der darauf folgende, stark genaeherte sehr klein, der 3te von der +Groesse +des ersten, die folgenden vom 4 - 8ten sehr kurz und +ungefaehr +von gleicher Bildung, die beiden letzten, welche wieder etwas +laenger +sind, stehen ziemlich weit nach innen +gerueckt +. Der Kopf oben +ueberall +netzaderig-runzlig, Wangen und +Schlaefe +dagegen fein runzlig, etwas +glaenzend +, durch einen scharfen Seitenrand begrenzt. Die Netzaugen klein aber deutlich. Der Mittelleib weicht in seiner Bildung und Sculptur von dem Arbeiter durch mehrere Punkte ab. Die Trennung des Pronotum's von dem Mesonotum ist durch eine tiefe, roth durchscheinende Querfurche bewirkt, letzteres aber in derselben Weise von dem Metanotum geschieden. Das Mesonotum vorne und an der Spitze +voellig +glatt, in der Mitte ziemlich fern und verworren runzlig; die beiden Dorne des Metanotum etwas mehr in die +Hoehe +gerichtet. Die Knoten des Hinterleibs zeigen genau die Bildung, welche sie beim Arbeiter haben, jedoch ist der hintere auf 4er Unterseite mit einer kleinen Spitze versehen. Das lste Segment an der Spitze, die +uebrigen +ganz roth; bei dem Isten Segment zieht sich die rothe Farbe auch am Seitenrande bis zur Basis des Segments hinauf; auf der Bauchseite ist die rothe Firbung dieselbe. Die Beine stimmen genau mit denen der Arbeiter +ueberein +, sie sind roth, die vordersten +Hueften +jedoch an der Vorderseite +braeunlich +. + + + + +Diese Art scheint sehr selten zu seyn, von dem Arbeiter habe ich anfangs Juny im Siebengebirge ein +Stueck +geschoepft +, und bei Aachen habe ich das einzige +tmgefluegelte +Weibchen gefangen. + + + + \ No newline at end of file diff --git a/data/38/A0/A1/38A0A1E7737A7C3064D693922A4DC9EB.xml b/data/38/A0/A1/38A0A1E7737A7C3064D693922A4DC9EB.xml new file mode 100644 index 00000000000..9dbdad0c2de --- /dev/null +++ b/data/38/A0/A1/38A0A1E7737A7C3064D693922A4DC9EB.xml @@ -0,0 +1,102 @@ + + + +Targeting a portion of central European spider diversity for permanent preservation + + + +Author + +Candek, Klemen + + + +Author + +Gregoric, Matjaz + + + +Author + +Kostanjsek, Rok + + + +Author + +Frick, Holger + + + +Author + +Kropf, Christian + + + +Author + +Kuntner, Matjaz + +text + + +Biodiversity Data Journal + + +2013 + +1 + + +980 +980 + + + + +http://dx.doi.org/10.3897/BDJ.1.e980 + +journal article +http://dx.doi.org/10.3897/BDJ.1.e980 +1314-2828--980 + + + + +Dipoena melanogaster (C. L. Koch, 1837) + + + +Materials + + +Occurrence: recordedBy: + +Kuntner, +Gregoric +, +Candek +, +Kralj-Fiser +, Cheng + +; sex: +1 female +; Location: locationID: SI41; country: +Slovenia +; locality: +Socerb, Osp +; minimumElevationInMeters: 116; maximumElevationInMeters: 116; decimalLatitude: +45.5819 +; decimalLongitude: +13.8558 +; Event: eventDate: +2012-06-07 +; habitat: trail from Socerb to Osp + + + + + \ No newline at end of file diff --git a/data/38/A0/B7/38A0B776A2AB29B510E9B93233A54B76.xml b/data/38/A0/B7/38A0B776A2AB29B510E9B93233A54B76.xml new file mode 100644 index 00000000000..3763a933d3a --- /dev/null +++ b/data/38/A0/B7/38A0B776A2AB29B510E9B93233A54B76.xml @@ -0,0 +1,89 @@ + + + +Checklist of British and Irish Hymenoptera - Sawflies, ' Symphyta' + + + +Author + +Liston, Andrew D. + + + +Author + +Knight, Guy T. + + + +Author + +Sheppard, David A. + + + +Author + +Broad, Gavin R. + + + +Author + +Livermore, Laurence + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1168 +1168 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1168 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1168 +1314-2828-2-1168 + + + + +Nematinae Thomson, 1871 + + + +Notes + +Unplaced species of +Nematinae +: + + +Nematus placidus +Cameron, 1878 + + +Placed by +Konow (1905) +as a synonym of +Pristiphora leucopodia +(Hartig, 1837), a species which has never been found in the British Isles. Konow probably did not examine the type of +Nematus placidus +, which according to +Benson (1943b) +, is lost. + + + + \ No newline at end of file diff --git a/data/38/A1/63/38A1635115C205162B6629C4C8F62DE2.xml b/data/38/A1/63/38A1635115C205162B6629C4C8F62DE2.xml new file mode 100644 index 00000000000..a2fd2c31dc6 --- /dev/null +++ b/data/38/A1/63/38A1635115C205162B6629C4C8F62DE2.xml @@ -0,0 +1,60 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Musca nemorum +[ +spec. nov. +] + + + +M. antennis setariis tomentosa, abdomine segmento luteo cingulisque tribus albis, segmento primo lateribus luteo. +Fn. svec. +1078. +Mer. eur. t. +2. +Reaum. ins. +3. +t. +31. +f. +8. +Alb. ins. t. +3. +f. M. L. + + + +Habitat in +Europa. + + + + \ No newline at end of file diff --git a/data/38/A1/B1/38A1B1B47DF420D7ADF69EBE026ECAD5.xml b/data/38/A1/B1/38A1B1B47DF420D7ADF69EBE026ECAD5.xml new file mode 100644 index 00000000000..182adb00b2a --- /dev/null +++ b/data/38/A1/B1/38A1B1B47DF420D7ADF69EBE026ECAD5.xml @@ -0,0 +1,94 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part A) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +252 +342 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Artemisia nilotica +Linnaeus + +, + +Centuria I Plantarum + +: 27. 1755 + + +. + + + +"Habitat in Aegypto. D. Hasselquist." RCN: 6456. + + + + +Lectotype +(Humphries in Jarvis & Turland in +Taxon +47: 354. 1998): +Hasselquist +, Herb. Linn. No. 1014.6 ( +LINN +; +iso- +LINN +1014.3, +UPS +) + +. + + + + +Current name: + + +Cotula anthemoides + +L. + +( +Asteraceae +). + + + + \ No newline at end of file diff --git a/data/38/A1/E6/38A1E631DADCCB8A36D476D44606134C.xml b/data/38/A1/E6/38A1E631DADCCB8A36D476D44606134C.xml new file mode 100644 index 00000000000..8be188bd111 --- /dev/null +++ b/data/38/A1/E6/38A1E631DADCCB8A36D476D44606134C.xml @@ -0,0 +1,80 @@ + + + +Guide to the littoral zone vascular flora of Carolina bay lakes (U. S. A.) + + + +Author + +Howell, Nathan + + + +Author + +Krings, Alexander + + + +Author + +Braham, Richard R + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +7964 +7964 + + + + +http://dx.doi.org/10.3897/BDJ.4.e7964 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e7964 +1314-2828-4-7964 + + + + +Rhexia virginica L. + + + + +Rhexia virginica +Taxon concept: [> +R. virginica L. var. purshii +- RAB;> +R. virginica L. var. virginica +; = GW, Weakley] + + + +Distribution +Little Singletary Lake (Infrequent): Howell LISI - 47 (NCSC!) + + +Notes + +Perennial herbs. Eulittoral zone ( +NLSM-T +, +NLSS-C +). +May-Oct +. Fig. 171 + + + + \ No newline at end of file diff --git a/data/38/A2/15/38A21511CD53A280B5D86C3C36A40AD3.xml b/data/38/A2/15/38A21511CD53A280B5D86C3C36A40AD3.xml new file mode 100644 index 00000000000..491e056cd49 --- /dev/null +++ b/data/38/A2/15/38A21511CD53A280B5D86C3C36A40AD3.xml @@ -0,0 +1,162 @@ + + + +Order Carnivora + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +532 +628 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Leopardus pajeros +(Desmarest 1816) + + + + + + + +[Felis] pajeros +Desmarest 1816 + +, +Nouv. Dict. Hist. Nat., (2), Vol. 6: 114 + +. + + + + +Type Locality: + +"Pampas de +Buenos Ayres +entre los 35 y 36 grados" [ +Argentina +]. + + + + + +Vernacular Names: +Pampas cat +. + + + + +Subspecies: +: + + +Subspecies + +Leopardus pajeros +subsp. +pajeros +Desmarest 1816 + + + +Subspecies + +Leopardus pajeros +subsp. +budini +Pocock 1941 + + + +Subspecies + +Leopardus pajeros +subsp. +garleppi +Matschie 1912 + + + +Subspecies + +Leopardus pajeros +subsp. +steinbachi +Pocock 1941 + + + +Subspecies + +Leopardus pajeros +subsp. +thomasi +Lönnberg 1913 + + + + + +Distribution: +Argentina +, +Bolivia +, +Chile +, +Ecuador +, +Peru +. + + + + +Conservation: +CITES +– Appendix II. + + + + +Discussion: +See comments under genus, see also García-Perea (1994). + + + + \ No newline at end of file diff --git a/data/38/A3/10/38A31079ADE4481422E1151D6FB78280.xml b/data/38/A3/10/38A31079ADE4481422E1151D6FB78280.xml new file mode 100644 index 00000000000..58ca8c7428a --- /dev/null +++ b/data/38/A3/10/38A31079ADE4481422E1151D6FB78280.xml @@ -0,0 +1,76 @@ + + + +Hornmilben (Oribatida) [pages 102 to 148] + + + +Author + +Weigmann, G. + + + +Author + +Miko, L. + +text + + +2006 +Goecke & Evers + +Keltern + + + +Hornmilben (Oribatida) [Dahl, Tierwelt Deutschlands, Teil 76] + + + +102 +148 + + + + +http://www.goeckeevers.de/verlag/dahl.html + +book chapter +Weigmann2006pp102to148 + + + + + +Steganacarus +(Steganacarus) herculeanus + +Willmann, 1953 [66e-g] + + + + +Syn., Tax.: +Steganacarus herculeanus +Willmann, 1953. Balogh & Mahunka 1983 (B); Niedbala 1992 (B). + + + + +Oekologie +: +Waldboeden +; auch alpin + + + + +Verbreitung: Frankreich, +Oesterreich +. + + + + \ No newline at end of file diff --git a/data/38/A3/7D/38A37DBCF131078D5C80144690AFBE95.xml b/data/38/A3/7D/38A37DBCF131078D5C80144690AFBE95.xml new file mode 100644 index 00000000000..1d2175cc8b8 --- /dev/null +++ b/data/38/A3/7D/38A37DBCF131078D5C80144690AFBE95.xml @@ -0,0 +1,89 @@ + + + +The Doryctinae (Braconidae) of Costa Rica: genera and species of the tribe Heterospilini + + + +Author + +Marsh, Paul M. + + + +Author + +Wild, Alexander L. + + + +Author + +Whitfield, James B. + +text + + +ZooKeys + + +2013 + +347 + + +1 +474 + + + + +http://dx.doi.org/10.3897/zookeys.347.6002 + +journal article +http://dx.doi.org/10.3897/zookeys.347.6002 +1313-2970-347-1 +52232D18DD784A84882CACA428B4A9D2 +52232D18DD784A84882CACA428B4A9D2 + + + + +Heterospilus azofeifai Marsh +sp. n. +Figure 17 + + + +Female. + +Body size: 4.5 mm. Color: head honey yellow; scape light brown without distinct lateral longitudinal brown stripe, flagellum brown (broken); mesosoma honey yellow, pronotum, mesopleuron dorsally and propodeum laterally brown; metasoma honey yellow, terga 1-2 brown laterally, terga 6-7 brown; legs yellow, base of hind tibia brown; wing veins including stigma brown. Head: vertex transversely striate; frons transversely striate; face weakly granulate; temple in dorsal view narrow and sloping +behind +eye, less than 1/2 eye width; malar space greater than 1/4 eye height; ocell-ocular distance about 1.5 times diameter of lateral ocellus;? flagellomeres (broken). Mesosoma: mesoscutal lobes granulate; notauli scrobiculate, meeting at scutellum in triangular rugose area; scutellum weakly granulate; prescutellar furrow with 1 distinct median cross carinae and 2 lateral weak carinae; mesopleuron smooth; precoxal sulcus weakly scrobiculate, shorter than mesopleuron; venter smooth; propodeum with basal median areas distinctly margined, smooth, basal median carina present, areola not distinctly margined, areolar area rugose, lateral areas rugose posteriorly, smooth or granulate anteriorly. Wings: fore wing vein r shorter than vein 3RSa, vein 1cu-a beyond vein 1M; hind wing vein SC+R present, vein M+CU shorter than vein 1M. Metasoma: first tergum costate, longer than apical width; second tergum costate, narrow with width about 4 times length; anterior transverse groove present, sinuate; posterior transverse groove absent; third tergum costate at base, granulate apically; terga 4-7 granulate; ovipositor longer than metasoma. + + + +Holotype female. +Top label (white, printed) - Costa Rica: Puntarenas [;] ACO, Golfito, RF Golfo Dulce [;] Est. Agujas, 250-300m [;] 3-24.vi.1999. J. Azofeifa [;] L.S. 276750-526550 #52840 [;] Red de Golpe; second label (red, partially printed and hand written) - HOLOTYPE [;] Heterospilus [;] azofeifai [;] P. Marsh. Deposited in ESUW. + + +Paratypes. +Known only from the holotype. + + +Comments. +This species is distinguished by the long ovipositor, yellow body and granulate apical metasomal terga. + + +Etymology. +Named for the collector of the holotype, J. Azofeifa. + + +Figure 17. +Heterospilus azofeifai +Marsh, sp. n., holotype. + + + + + \ No newline at end of file diff --git a/data/38/A4/43/38A443F5F1586DA1AD49E4A8BDBD38D5.xml b/data/38/A4/43/38A443F5F1586DA1AD49E4A8BDBD38D5.xml new file mode 100644 index 00000000000..b9663c55211 --- /dev/null +++ b/data/38/A4/43/38A443F5F1586DA1AD49E4A8BDBD38D5.xml @@ -0,0 +1,73 @@ + + + +An annotated checklist of the Cook Islands psyllids with keys to the species and two new records (Hemiptera, Psylloidea) + + + +Author + +Martoni, Francesco + + + +Author + +Brown, Samuel D. J. + +text + + +ZooKeys + + +2018 + +811 + + +91 +108 + + + + +http://dx.doi.org/10.3897/zookeys.811.28829 + +journal article +http://dx.doi.org/10.3897/zookeys.811.28829 +1313-2970-811-91 +7FC5DEBE45894AD48D7A69C5615FA737 + + + + +Trioza alifumosa Klyver, 1932 +Figures 11-20, 26 + + + + +Trioza alifumosa +Klyver, 1932: 96. + + + +Distribution. + +Reported on the Cook Islands in the present study. Known only from Rarotonga. Other locations include: French Polynesia (Marquesas, Fatu Hiva) ( +Klyver 1932 +). + + + +Host plant. + +Metrosideros collina +(J.R. Forst. & G. Forst.) A. Gray ( +Myrtaceae +). + + + + \ No newline at end of file diff --git a/data/38/A4/AD/38A4AD871C1AD1A8F304FF5D028BB2FD.xml b/data/38/A4/AD/38A4AD871C1AD1A8F304FF5D028BB2FD.xml new file mode 100644 index 00000000000..831be8dce0b --- /dev/null +++ b/data/38/A4/AD/38A4AD871C1AD1A8F304FF5D028BB2FD.xml @@ -0,0 +1,278 @@ + + + +Minimalist revision and description of 403 new species in 11 subfamilies of Costa Rican braconid parasitoid wasps, including host records for 219 species + + + +Author + +Sharkey, Michael J. +https://orcid.org/0000-0001-6201-7340 +The Hymenoptera Institute, 116 Franklin Ave., Redlands, CA, 92373, USA +msharkey@uky.edu + + + +Author + +Janzen, Daniel H. +Department of Biology, University of Pennsylvania, Philadelphia, PA 19104 - 6018, USA + + + +Author + +Hallwachs, Winnie +Department of Biology, University of Pennsylvania, Philadelphia, PA 19104 - 6018, USA + + + +Author + +Chapman, Eric G. +Department of Entomology, University of Kentucky, Lexington, KY 40546 - 0091, USA + + + +Author + +Smith, M. Alex +https://orcid.org/0000-0002-8650-2575 +Department of Integrative Biology, University of Guelph and Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Dapkey, Tanya +Academy of Natural Sciences, 1900 Benjamin Franklin Parkway, Philadelphia, PA 19103, USA + + + +Author + +Brown, Allison +Academy of Natural Sciences, 1900 Benjamin Franklin Parkway, Philadelphia, PA 19103, USA + + + +Author + +Ratnasingham, Sujeevan +Academy of Natural Sciences, 1900 Benjamin Franklin Parkway, Philadelphia, PA 19103, USA + + + +Author + +Naik, Suresh +Academy of Natural Sciences, 1900 Benjamin Franklin Parkway, Philadelphia, PA 19103, USA + + + +Author + +Manjunath, Ramya +Academy of Natural Sciences, 1900 Benjamin Franklin Parkway, Philadelphia, PA 19103, USA + + + +Author + +Perez, Kate +Academy of Natural Sciences, 1900 Benjamin Franklin Parkway, Philadelphia, PA 19103, USA + + + +Author + +Milton, Megan +Academy of Natural Sciences, 1900 Benjamin Franklin Parkway, Philadelphia, PA 19103, USA + + + +Author + +Hebert, Paul +Academy of Natural Sciences, 1900 Benjamin Franklin Parkway, Philadelphia, PA 19103, USA + + + +Author + +Shaw, Scott R. +Department of Ecosystem Science, University of Wyoming, 1000 East University Avenue, Laramie, Wyoming 82071, USA + + + +Author + +Kittel, Rebecca N. +https://orcid.org/0000-0003-0032-5764 +Museum Wiesbaden, Hessisches Landesmuseum fuer Kunst und Natur, Friedrich-Ebert-Allee 2, 65185 Wiesbaden, Germany + + + +Author + +Solis, M. Alma +https://orcid.org/0000-0001-6379-1004 +Systematic Entomology Laboratory, Beltsville Agriculture Research Center, Agricultural Research Service, U. S. Department of Agriculture, c / o National Museum Natural History, MRC 168, Smithsonian Institution, P. O. Box 37012, Washington, DC, 20013 - 7012, USA + + + +Author + +Metz, Mark A. +Systematic Entomology Laboratory, Beltsville Agriculture Research Center, Agricultural Research Service, U. S. Department of Agriculture, c / o National Museum Natural History, MRC 168, Smithsonian Institution, P. O. Box 37012, Washington, DC, 20013 - 7012, USA + + + +Author + +Goldstein, Paul Z. +Systematic Entomology Laboratory, Beltsville Agriculture Research Center, Agricultural Research Service, U. S. Department of Agriculture, c / o National Museum Natural History, MRC 168, Smithsonian Institution, P. O. Box 37012, Washington, DC, 20013 - 7012, USA + + + +Author + +Brown, John W. +Division of Entomology, PO Box 37012 12. National Museum of Natural History E 515 MRC 127, Washington, DC 20013 - 7012, USA + + + +Author + +Quicke, Donald L. J. +Department of Biology, Faculty of Life Sciences, Chulalongkorn University, Bangkok, Thailand + + + +Author + +Achterberg, C. van +https://orcid.org/0000-0002-6495-4853 +Naturalis Biodiversity Center, Postbus 9517, 2300 RA Leiden, The Netherlands + + + +Author + +Brown, Brian V. +https://orcid.org/0000-0001-6367-6057 +Department of Entomology, Natural History Museum of Los Angeles County, 900 Exposition Boulevard, Los Angeles, CA, 90007, USA + + + +Author + +Burns, John M. +Division of Entomology, PO Box 37012 12. National Museum of Natural History E 515 MRC 127, Washington, DC 20013 - 7012, USA + +text + + +ZooKeys + + +2021 + +2021-02-02 + + +1013 + + +1 +665 + + + + +http://dx.doi.org/10.3897/zookeys.1013.55600 + +journal article +http://dx.doi.org/10.3897/zookeys.1013.55600 +1313-2970-1013-1 +CFDCEFBB523040339D46E302F66E9886 +E4329863A39E5EEBA395938413BDD579 + + + + +Aleiodes annhowdenae Sharkey +sp. nov. +Figure 385 + + + +Diagnostics. +BOLD:AAM5664. Consensus barcode. AATTTTATATTTTTTATTTGGAATATGAKCAGGRATAATCGGTATATCGATAAGATTAATTATTCGCATGGAATTAAGAACTAGAGGAAGAATTTTAAAAAATGATCAAATTTATAATAGAGTAGTAACTTTACATGCTTTTATTATAATTTTTTTTATAGTAATACCTATTATAATTGGAGGATTTGGTAATTGATTAATTCCACTAATATTAGGGGCTCCAGATATAGCTTTCCCRCGAATAAATAATATAAGATTTTGACTTTTAATCCCATCTTTATTATTACTTCTAAACAGGGGTATTATTAACTCAGGGGTGGGAACAGGGTGAACAATATACCCTCCCCTTTCTTCATTAATTGGCCATAATGGAATTTCAGTAGATATATCRATTTTTTCTCTTCATTTAGCGGGGGCTTCTTCAATTATAGGGGCTATTAATTTTATTTCTACTATTTTTAATATAAATTTATTAATAATTAAAATAAATCAATTRACTTTACTTACTTGATCAATTTTAATTACRACAATTTTACTACTTTTATCTTTACCAGTTTTAGCAGGGGCAATTACAATATTACTAACAGATCGAAATTTAAACACWRRWTTTTTTGATTTTTCCGGAGGGGGAGACCCAATTTTATTTCAACACTTA. + + +Holotype ♀. + +Alajuela, Sector San Cristobal, Finca San Gabriel, +10.87766 +, +-85.39343 +, 645 meters, caterpillar collection date: 23/ix/2013, wasp eclosion date: 12/x/2013. Depository: CNC. + + + +Host data +. + + +Eutomopepla artena + +( +Geometridae +) feeding on + +Pleuranthodendron lindenii + +( +Salicaceae +). + + + +Host caterpillar and holotype wasp voucher codes +. + +13-SRNP-4963, DHJPAR0053665. + + + +Paratypes. +None. + + +Other material. +Four specimens in the same BIN (BMNHE897761, BMNHE897815, BMNHE897843, BMNHE897846) were collected in Belize. They were not examined. + + +Etymology. + + +Aleiodes annhowdenae + +is named in honor of Ann +Howden's +long-appreciated contributions to publicity for ACG, GDFCF, and now, BioAlfa. + + + +Figure 385. + +Aleiodes annhowdenae + +, holotype. + + + + + \ No newline at end of file diff --git a/data/38/A4/E4/38A4E4B6A955F83C52DB588EF2E99E89.xml b/data/38/A4/E4/38A4E4B6A955F83C52DB588EF2E99E89.xml new file mode 100644 index 00000000000..57e3765df96 --- /dev/null +++ b/data/38/A4/E4/38A4E4B6A955F83C52DB588EF2E99E89.xml @@ -0,0 +1,55 @@ + + + +Catalogue of hymenopterous insects collected by Mr. A. R. Wallace at the Islands of Aru and Key. + + + +Author + +Smith, F. + +text + + +Journal of the Proceedings of the Linnean Society of London, Zoology + + +1859 + +3 + + +132 +158 + + + + +http://antbase.org/ants/publications/10342/10342.pdf + +journal article +10342 +03D4C4E8-74F9-42F2-8FD1-00A6DC22903A + + + + +7. +Polyrhachis scutulatus +. + + + +P. niger, fortiter politus et lucidus, metathorace petiolique squamula dente longo curvato acuto in latere utroque, pedibus nigro-ferrugineis. +Worker. Length 2 3 / 4 lines. Black and very smooth and shining; the legs dark ferruginous. Thorax: the disk expanded, slightly convex above, with the margins acute and curving upwards; the anterior margin transverse, rather wider than the head, with the lateral angles slightly curved forwards, and very acute; the lateral margins of the prothorax curved backwards and inwards; the margins of the mesothorax are rounded; the pro- and mesothorax highly polished above, forming an escutcheon-shaped disk; the metathorax opake, and sprinkled with a few short glittering hairs, armed posteriorly with two long very acute spines, divergent and directed backwards. Abdomen globose; the scale of the petiole with two long curved acute spines, directed backwards to the curve of the abdomen. + + + +Hab. +Aru +. + + + + \ No newline at end of file diff --git a/data/38/A5/99/38A599704B9F5AC592A892D0DAE130A2.xml b/data/38/A5/99/38A599704B9F5AC592A892D0DAE130A2.xml new file mode 100644 index 00000000000..2adab93c8d0 --- /dev/null +++ b/data/38/A5/99/38A599704B9F5AC592A892D0DAE130A2.xml @@ -0,0 +1,216 @@ + + + +? An illustrated catalogue of the type specimens of Lepidoptera housed in the Zoological Museum Hamburg (ZMH): Part II. superfamily Papilionoidea + + + +Author + +Zahiri, Reza +https://orcid.org/0000-0001-6274-6973 +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany & Canadian Food Inspection Agency, Ottawa Plant Laboratory, Entomology Unit, Bldg. 18, 960 Carling Ave., K 1 A 0 C 6, Ottawa, Ontario, Canada +reza.zahiri@gmail.com + + + +Author + +Nazari, Vazrick +https://orcid.org/0000-0001-9064-8959 +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany + + + +Author + +Rajaei, Hossein +https://orcid.org/0000-0002-3940-3734 +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany + + + +Author + +Wiemers, Martin +https://orcid.org/0000-0001-5272-3903 +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany + + + +Author + +Fatahi, Maryam +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany + + + +Author + +Seidel, Matthias +https://orcid.org/0000-0002-4913-8778 +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany + + + +Author + +Dalsgaard, Thure +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany + + + +Author + +Husemann, Martin +https://orcid.org/0000-0001-5536-6681 +Leibniz Institute for the Analysis of Biodiversity Change, Martin-Luther-King Platz 3, 20146 Hamburg, Germany + +text + + +Evolutionary Systematics + + +2021 + +2021-08-20 + + +5 + + +2 + + +193 +261 + + + + +http://dx.doi.org/10.3897/evolsyst.5.63435 + +journal article +http://dx.doi.org/10.3897/evolsyst.5.63435 +2535-0730-2-193 +984E15D880E04B7DA84F92BB0AD4EA73 +21773559522D5D9DA4B1A7DA51E4F2A6 + + + + +?147. +Hipparchia persiscana Verity, 1937 + + + +Original combination. + +" + +Eumenis allionii + +, G.-H. = + +Hipparchia fatua + +Freyer, +persiscana +, nom. nov." Verity, 1937 Ent. Rec. 49: 100. + + + +Current combination. + + + +Hipparchia fatua persiscana + +(Verity, 1937) + +. + + + +Current status. +Valid subspecies. + + +Type material. + +Syntypes 31?? (ZMH 827683-827713) (Fig. +147 +). "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827683"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827684"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827685"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827686"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827687"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827688"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827689"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827690"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827691"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827692"; "Iran / Keredj 1800 m / 21.8.1936 / Brandt" // +"Cotypus" +// "ssp. persicana / Vrty" // "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827693"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827694"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827695"; "Iran / Keredj 1800 m / 25/8 1936 / Brandt" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827696"; "Iran / Keredj 1800 m / 25/8 1936 / Brandt" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827697"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827698"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827699"; "Iran / Keredj 1800 m / 25/8 1936 / Brandt" // +"201" +// +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827700"; "Iran / Keredj 1800 m / 21/8 1936 / Brandt" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827701"; "Iran / Keredj 1200 m / 1936 / Brandt" // "1600 25/VIII" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20, 1960" // "ZMH 827702"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827703"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827704"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827705"; "Iran / Keredj (1200 m.) / 1936 / Brandt" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20, 1960" // "ZMH 827706"; "Iran / Keredj 1600 m / 25/8 1936 / Brandt" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827707"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20, 1960" // "ZMH 827708"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827709"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827710"; "Iran / Keredj 1200 m / 1936 / Brandt" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20 - 60" // "ZMH 827711"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20, 1960" // "ZMH 827712"; "Iran / Keredj 1600 m / VIII 1936 / leg. F. Brandt / coll. Bytinski-Salz" // +"Cotypus" +// "Coll. Bytinski-Salz / Eing. Nr. 20, 1960" // "ZMH 827713". + + + +Type locality. +Iran: Tehran, "Keredj [Karaj], in the Elburz Mountains, at m. 1500 to 1600". + + + \ No newline at end of file diff --git a/data/38/A5/AD/38A5AD1758417D482F6E9B41A3B00370.xml b/data/38/A5/AD/38A5AD1758417D482F6E9B41A3B00370.xml new file mode 100644 index 00000000000..d3f9296178d --- /dev/null +++ b/data/38/A5/AD/38A5AD1758417D482F6E9B41A3B00370.xml @@ -0,0 +1,71 @@ + + + +Cyanobacteria of Greece: an annotated checklist + + + +Author + +Gkelis, Spyros + + + +Author + +Ourailidis, Iordanis + + + +Author + +Panou, Manthos + + + +Author + +Pappas, Nikos + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +10084 +10084 + + + + +http://dx.doi.org/10.3897/BDJ.4.e10084 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e10084 +1314-2828-4-10084 + + + + +Brachytrichia quoyi Bornet & Flahault, 1886 + + + + +Brachytrichia quiyi + + + +Notes + +Anagnostidis 1968 + + + + \ No newline at end of file diff --git a/data/38/A6/15/38A6152DABE336143A3080821EBD0ECC.xml b/data/38/A6/15/38A6152DABE336143A3080821EBD0ECC.xml new file mode 100644 index 00000000000..af71be2977a --- /dev/null +++ b/data/38/A6/15/38A6152DABE336143A3080821EBD0ECC.xml @@ -0,0 +1,203 @@ + + + +Order Rodentia - Family Cricetidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 2 + + + +955 +1189 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316535 + + + + + +Caryomys inez +(Thomas 1908) + + + + + + + +[Microtus (Eothenomys)] inez +Thomas 1908 + +, +Abstr. Proc. Zool. Soc. Lond., 1908 (63): 45 + +. + + + + +Type Locality: + +China +, +Shanxi +(Shansi), mtns +12 mi +( +19 km +) NW Kolanchow, +7000 ft +( + +2134 m + +). + + + + + +Vernacular Names: +Inez's Red-backed Vole +. + + + + +Synonyms: + +Caryomys nux +(Thomas 1910) + +. + + + + +Distribution: +N +Sichuan +and SE +Shaanxi +through +Shanxi +provinces, +China +, possibly farther east. + + + + +Conservation: +IUCN +– Lower Risk (lc) as + +Eothenomys inez + +. + + + + +Discussion: +Following + +Hinton (1926 +a +) + +, + +inez + +was synonymized with + +Clethrionomys rufocanus + +( +Ellerman and Morrison-Scott, 1951 +; +Gromov and Polyakov, 1977 +), but its distinctive status is well documented, typically within + +Eothenomys + +(G. M. Allen, 1940; + +Corbet, 1978 +c + +; +Corbet and Hill, 1992 +; + +Kaneko, 1992 +c + +). + +Hinton (1926 +a +) + +and +Ellerman and Morrison-Scott (1951) +allocated + +nux + +to + +Clethrionomys rufocanus shanseius + +, but G. M. Allen (1940) treated it as a subspecies of + +Eothenomys inez + +. Kaneko’s (1991) morphometric analysis identified the +holotype +of + +nux + +as an example of + +inez + +, as concluded earlier by A. B. Howell (1929). Kaneko restricted the range to +Shaanxi +and +Shanxi +provinces, but +Zhang et al. (1997) +mapped a far broader distribution. + + + + \ No newline at end of file diff --git a/data/38/A6/43/38A643E4EE2151C6BAD67477BFADA556.xml b/data/38/A6/43/38A643E4EE2151C6BAD67477BFADA556.xml new file mode 100644 index 00000000000..dbde01500f4 --- /dev/null +++ b/data/38/A6/43/38A643E4EE2151C6BAD67477BFADA556.xml @@ -0,0 +1,124 @@ + + + +An updated checklist of the marine fish fauna of Redang Islands, Malaysia + + + +Author + +Du, Jianguo + + + +Author + +Loh, Kar-Hoe + + + +Author + +Hu, Wenjia + + + +Author + +Zheng, Xinqing + + + +Author + +Affendi, Yang Amri + + + +Author + +Ooi, Jillian Lean Sim + + + +Author + +Ma, Zhiyuan + + + +Author + +Rizman-Idid, Mohammed + + + +Author + +Chan, Albert Apollo + +text + + +Biodiversity Data Journal + + +2019 + +7 + + +47537 +47537 + + + + +http://dx.doi.org/10.3897/BDJ.7.e47537 + +journal article +http://dx.doi.org/10.3897/BDJ.7.e47537 +1314-2828-7-e47537 +F940F7FD0A3541E98BDD33F83C2369D5 +AE1BE74780565E8D9B3522053F3B0983 + + + + +Stegestes lividus (Forster, 1801) + + + +Materials + + +Type status: +Other material +. +Occurrence: +occurrenceID: BDJ_12482_255; +Location: +country: +Malaysia +; locality: +Redang islands +; +Identification: +identifiedBy: +Loh KH and Du Jianguo + + + + +Notes + +s: + +Stagestes lividus +Yusuf et al. 2001 + +. + + + + \ No newline at end of file diff --git a/data/38/A6/7C/38A67C78E330C0D5562DFE3ED34E416C.xml b/data/38/A6/7C/38A67C78E330C0D5562DFE3ED34E416C.xml new file mode 100644 index 00000000000..58f467b47dd --- /dev/null +++ b/data/38/A6/7C/38A67C78E330C0D5562DFE3ED34E416C.xml @@ -0,0 +1,86 @@ + + + +The high alpine bee fauna (Hymenoptera: Apoidea) of the Zillertal Alps, Austria + + + +Author + +Bossert, Silas + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1115 +1115 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1115 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1115 +1314-2828-2-1115 + + + + +Bombus mendax Gerstaecker, 1869 + + + +Materials + + +Type status: +Other material +. Occurrence: recordedBy: +S. Bossert +; individualCount: +1 +; sex: +1 queen +; Location: country: +Austria +; stateProvince: Tyrol; locality: +Zemmgrund +; verbatimElevation: 2079 m; decimalLatitude: +47.0256794 +; decimalLongitude: +11.8167508 +; Event: samplingProtocol: +manual catch +; eventDate: +07-06-13 +; habitat: alpine meadow + + + + +Distribution + +Palaearctic ( +Williams 1998 +, +Williams 2014 +). +Amiet (1996) +reports +Bombus mendax +to occur above 1500 m a.s.l. and +Neumayer (1998) +proposes the species to exceed even 3000 m a.s.l. + + + + \ No newline at end of file diff --git a/data/38/A6/9D/38A69D719548008E7BC03C0A926BE74D.xml b/data/38/A6/9D/38A69D719548008E7BC03C0A926BE74D.xml new file mode 100644 index 00000000000..7589121033c --- /dev/null +++ b/data/38/A6/9D/38A69D719548008E7BC03C0A926BE74D.xml @@ -0,0 +1,247 @@ + + + +Info Flora Schweiz - Apiaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/apiaceae.html + +url + + + + + +Laserpitium nitidum +Zanted. + + + + + +Art ISFS: 227800 Checklist: 1025870 +Apiaceae +Laserpitium +Laserpitium nitidum Zanted. + + +Zusammenfassung +KEINE ANGABE + + + +Oekologie + + + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + +KEINE ANGABE + + +
+
+
+
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F--Lichtzahl L--Salzzeichen--
Reaktionszahl R--Temperaturzahl T--
+Naehrstoffzahl +N +-- +Kontinentalitaetszahl +K +--
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Laserpitium nitidum +Zanted. + + + + + +Volksname + + + +Deutscher Name: -- Nom +francais +: -- Nome italiano: -- + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Laserpitium nitidum Zanted. + + +Checklist 2017 + +227800
= +Laserpitium nitidum Zanted. + + +Index synonymique 1996 + +227800
= +Laserpitium nitidum Zanted. + + +Landolt 1977 + +2167
= +Laserpitium nitidum Zanted. + + +SISF/ISFS 2 + +227800
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Status Indigenat +: - + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein + + +
+
\ No newline at end of file diff --git a/data/38/A7/66/38A766EB610656C59F2915C25C6FC5A2.xml b/data/38/A7/66/38A766EB610656C59F2915C25C6FC5A2.xml new file mode 100644 index 00000000000..e1bb9c8299b --- /dev/null +++ b/data/38/A7/66/38A766EB610656C59F2915C25C6FC5A2.xml @@ -0,0 +1,92 @@ + + + +Diversity pattern of insects from Macao based on an updated species checklist after 25 years + + + +Author + +Xian, Chunlan +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China + + + +Author + +Leong, Chi Man +Department of Life Sciences, Faculty of Science and Technology, Beijing normal university - Hong Kong Baptist University United International College, Zhuhai, China & Macao Entomological Society, Estrada Coronel Nicolau de Mesquita, Macao SAR, China + + + +Author + +Luo, Jiuyang +https://orcid.org/0000-0002-2748-9534 +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China + + + +Author + +Jia, Fenglong +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China + + + +Author + +Han, Hongxiang +Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, China +hanhx@ioz.ac.cn + + + +Author + +Xie, Qiang +https://orcid.org/0000-0001-6376-8808 +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China +xieq8@mail.sysu.edu.cn + +text + + +Biodiversity Data Journal + + +2024 + +2024-04-05 + + +12 + + +118110 +118110 + + + + +http://dx.doi.org/10.3897/BDJ.12.e118110 + +journal article +http://dx.doi.org/10.3897/BDJ.12.e118110 +1314-2828-12-e118110 +57B0CE31B4055266A115FC1275D70C79 + + + + +Eutelia adulatricoides (Mell, 1943) + + + +Notes + +Li (2023) + + + + \ No newline at end of file diff --git a/data/38/A7/D3/38A7D3AFA28340E11B12734E339097AC.xml b/data/38/A7/D3/38A7D3AFA28340E11B12734E339097AC.xml new file mode 100644 index 00000000000..b91b7c538bc --- /dev/null +++ b/data/38/A7/D3/38A7D3AFA28340E11B12734E339097AC.xml @@ -0,0 +1,113 @@ + + + +Pictorial key to species of the genus Ropalidia Guerin-Meneville, 1831 (Hymenoptera, Vespidae) from China, with description of one new species + + + +Author + +Tan, Jiang-Li + + + +Author + +Van Achterberg, Kees + + + +Author + +Chen, Xue-Xin + +text + + +ZooKeys + + +2014 + +391 + + +1 +35 + + + + +http://dx.doi.org/10.3897/zookeys.391.6606 + +journal article +http://dx.doi.org/10.3897/zookeys.391.6606 +1313-2970-391-1 +00BA115D65D44A0C933CC29F56236DEA + + + + +Ropalidia ornaticeps (Cameron, 1900) +rec. n. +Figure 2B + + + + +Icaria ornaticeps +Cameron, 1900: 496. Type locality: India. + + +Ropalidia flavopicta ornaticeps +; +van der Vecht 1962 +: 49. + + +Ropalidia ornaticeps +; +Yoshikawa et al. 1969 +: 167; +Kojima 1996a +: 325. + + + +Specimens examined. + +CHINA: 1 ♀ (CATAS), Nada, Danzhou, Hainan, +19°5'17"N +, +109°34'50"E +, 143 m. VIETNAM: 46 ♀ + 1 ♂ (RMNH, IEBR), +Dong +Nai, +Cat +Tien N.P., Mal. traps, x.2005 & iv.-v.2007, C van Achterberg & R de Vries; 1 ♂ (RMNH), Thua Thien +Hue +, Phong +Dien +N.R., 23.iii.-6.iv.2001, Mal. traps 6-9, C van Achterberg & R de Vries. THAILAND: 3 ♀, (RMNH), Chiang Khan, 17.vii.1986, R Hensen, with a label "Ropalidia ornaticeps (Cameron, 1900), det. J Kojima, 1996". + + + +Remarks. + +The clypeus is completely yellow, but sometimes with a small black spot; the occipital carina is variable, sometimes the carina is bent anteriorly as in +Ropalidia flavopicta +. + + + +Distribution. + +China (Hainan); Cambodia; India, Malay Peninsula; Myanmar; Thailand; Vietnam. ( +Kojima and Carpenter 1997 +and updated to 2006, +Kojima et al. 2007 +). + + + + \ No newline at end of file diff --git a/data/38/A8/08/38A8087340EA5C3A91BF07AC312FBD9D.xml b/data/38/A8/08/38A8087340EA5C3A91BF07AC312FBD9D.xml new file mode 100644 index 00000000000..e001f5d5abf --- /dev/null +++ b/data/38/A8/08/38A8087340EA5C3A91BF07AC312FBD9D.xml @@ -0,0 +1,155 @@ + + + +A new generic system for the pantropical Caesalpinia group (Leguminosae) + + + +Author + +Gagnon, Edeline +https://orcid.org/0000-0003-3212-9688 +Institut de recherche en biologie vegetale and Departement de sciences biologiques, Universite de Montreal, H 1 X 2 B 2, Montreal, Quebec, Canada +edeline.gagnon@gmail.com + + + +Author + +Bruneau, Anne +Institut de recherche en biologie vegetale and Departement de sciences biologiques, Universite de Montreal, H 1 X 2 B 2, Montreal, Quebec, Canada + + + +Author + +Hughes, Colin E. +Department of Systematic and Evolutionary Botany, University of Zuerich, 8008, Zuerich, Switzerland + + + +Author + +de Queiroz, Luciano Paganucci +Universidade Estadual de Feira de Santana, BR 116, Km 03, Campus Universitario, Feira de Santana 44031 - 460, Bahia, Brasil + + + +Author + +Lewis, Gwilym P. +Comparative Plant and Fungal Biology Department, Royal Botanic Gardens, Kew, Richmond, Surrey, TW 9 3 AB, United Kingdom + +text + + +PhytoKeys + + +2016 + +2016-10-12 + + +71 + + +1 +160 + + + + +http://dx.doi.org/10.3897/phytokeys.71.9203 + +journal article +http://dx.doi.org/10.3897/phytokeys.71.9203 +1314-2003-71-1 +FFA8FF9AFFEAFFDABA68757DFF9EFF8B +160340 + + + + +18.3 +Cenostigma gaumeri (Greenm.) E. Gagnon & G. P. Lewis +comb. nov. + + + +Basionym. + + +Caesalpinia gaumeri + +Greenm., Publ. Field Mus. Nat. Hist., Bot. Ser. 2: 330. 1912. + + + +Poincianella gaumeri + +(Greenm.) Britton & Rose, N. Amer. Fl. 23(5): 333. 1930. + + + + +Type +. + + + +MEXICO +, + +Yucatan + +, +Progresso +, +5 Mar 1899 +, +Millspaugh 1675 +( +holotype +F) + +. + + + +Poincianella guanensis + +Britton, N. Amer. Fl. 23(5): 333. 1930. + + + +Caesalpinia guanensis + +(Britton) +Leon +, Contr. Ocas. Mus. Hist. Nat. Colegio "De La Salle" 9: 12. 1950. + + + +Type. +CUBA +, + +Remates +de Guane + +, +Pinar del Rio +, +Apr 1926 +, +Fors 3965 +( +holotype +NY!) + +. + + + + \ No newline at end of file diff --git a/data/38/A8/40/38A84043F2D15707BCC5AA90DCC12423.xml b/data/38/A8/40/38A84043F2D15707BCC5AA90DCC12423.xml new file mode 100644 index 00000000000..5ca699191c2 --- /dev/null +++ b/data/38/A8/40/38A84043F2D15707BCC5AA90DCC12423.xml @@ -0,0 +1,119 @@ + + + +DNA barcodes reveal 63 overlooked species of Canadian beetles (Insecta, Coleoptera) + + + +Author + +Pentinsaari, Mikko + + + +Author + +Anderson, Robert + + + +Author + +Borowiec, Lech + + + +Author + +Bouchard, Patrice + + + +Author + +Brunke, Adam + + + +Author + +Douglas, Hume + + + +Author + +Smith, Andrew B. T. + + + +Author + +Hebert, Paul D. N. + +text + + +ZooKeys + + +2019 + +894 + + +53 +150 + + + + +http://dx.doi.org/10.3897/zookeys.894.37862 + +journal article +http://dx.doi.org/10.3897/zookeys.894.37862 +1313-2970-894-53 +D11503CA5A574067817904E0C8C162C8 +BAF8B2CC491254A3AC7E08368A2697B5 + + + + +Henoticus mycetoecus (Park, 1929) + + + +Distribution. + +Native to North America. Described from Illinois ( +Park 1929 +), also recorded from Iowa ( +Downie and Arnett 1996 +). + + + +Canadian records. +Ontario: Rouge National Urban Park, 18-Jun-2013 to 25-Jun-2013 (1 ex, CBG). + + +Diagnostic information + +(based on +Park (1929) +). Body length 1.8-2.0 mm. More or less uniformly red-brown, with legs, antennae, and medial part of elytra paler. Lateral margins of pronotum serrate, sublateral carinae absent. Posterior of pronotum with two deep foveae connected by a distinct basal groove. + + + +Bionomic notes. + +Park (1929) +collected the type specimens from decaying fruiting bodies of the polypore fungus + +Climacodon septentrionalis + +(Fr.) P. Karst. in a sugar maple forest. The Canadian specimen was caught with a Malaise trap in a patch of forest. + + + + \ No newline at end of file diff --git a/data/38/A8/AA/38A8AAAE3ACD5CC2A9D23E058A8E2CE0.xml b/data/38/A8/AA/38A8AAAE3ACD5CC2A9D23E058A8E2CE0.xml new file mode 100644 index 00000000000..9b5b8dbfa59 --- /dev/null +++ b/data/38/A8/AA/38A8AAAE3ACD5CC2A9D23E058A8E2CE0.xml @@ -0,0 +1,81 @@ + + + +Checklist of national key protected wild plants on the Qinghai-Tibetan Plateau + + + +Author + +Chen, Ronglian +University of Chinese Academy of Sciences, Beijing, China & Qinghai Provincial Key Laboratory of Crop Molecular Breeding, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, China + + + +Author + +Zhang, Faqi +Qinghai Provincial Key Laboratory of Crop Molecular Breeding, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, China + + + +Author + +Chen, Shilong +Qinghai Provincial Key Laboratory of Crop Molecular Breeding, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, China + + + +Author + +Chi, Xiaofeng +Qinghai Provincial Key Laboratory of Crop Molecular Breeding, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, China +xfchi@nwipb.cas.cn + +text + + +Biodiversity Data Journal + + +2023 + +2023-05-16 + + +11 + + +103289 +103289 + + + + +http://dx.doi.org/10.3897/BDJ.11.e103289 + +journal article +http://dx.doi.org/10.3897/BDJ.11.e103289 +1314-2828-11-e103289 +D2D96D0A93125BF2BD8A1911FBE4E783 + + + + +Phlegmariurus yunnanensis Ching, 1982 + + + +Conservation status +DD + + +Distribution +China + + +Notes +Endemic to Qinghai-Tibetan Plateau + + + \ No newline at end of file diff --git a/data/38/A8/AC/38A8ACF10820512DA425B22D284C1CE5.xml b/data/38/A8/AC/38A8ACF10820512DA425B22D284C1CE5.xml new file mode 100644 index 00000000000..464b84f5047 --- /dev/null +++ b/data/38/A8/AC/38A8ACF10820512DA425B22D284C1CE5.xml @@ -0,0 +1,98 @@ + + + +Taxonomic and nomenclatural notes on Chinese species of Sarcophaga Meigen, 1824 (Diptera, Sarcophagidae) + + + +Author + +Wang, Chao +https://orcid.org/0000-0001-7251-1860 +State Key Laboratory of Infectious Disease Prevention and Control, WHO Collaborating Centre for Vector Surveillance and Management, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China & School of Ecology and Nature Conservation, Beijing Forestry University, Beijing 100083, China + + + +Author + +Sun, Haoran +https://orcid.org/0000-0003-1785-4160 +School of Ecology and Nature Conservation, Beijing Forestry University, Beijing 100083, China + + + +Author + +Zhu, Weibing +https://orcid.org/0000-0002-9607-2513 +Center for Excellence in Molecular Plant Science, Chinese Academy of Sciences, Shanghai 200032, China + + + +Author + +Pape, Thomas +https://orcid.org/0000-0001-6609-0609 +Natural History Museum of Denmark, University of Copenhagen, Universitetsparken 15, DK- 2100, Copenhagen, Denmark + + + +Author + +Liu, Qiyong +State Key Laboratory of Infectious Disease Prevention and Control, WHO Collaborating Centre for Vector Surveillance and Management, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China +liuqiyong@icdc.cn + + + +Author + +Zhang, Dong +School of Ecology and Nature Conservation, Beijing Forestry University, Beijing 100083, China +ernest8445@163.com + +text + + +ZooKeys + + +2022 + +2022-06-24 + + +1108 + + +141 +159 + + + + +http://dx.doi.org/10.3897/zookeys.1108.83267 + +journal article +http://dx.doi.org/10.3897/zookeys.1108.83267 +1313-2970-1108-141 +939DAE085A6941C58EA9D0DDBF4BEF03 +244EDD960B8B51CFB70D0CF3C649F5DA + + + + +Subgenus +Sarcophaga Phallantha Rohdendorf, 1938 + + + + +Phallantha +Rohdendorf, 1938: 101. Type species: +Phallantha sichotealini +Rohdendorf, 1938, by original designation. + + + + \ No newline at end of file diff --git a/data/38/A8/E1/38A8E11EE37751AAECC369B60D87BDEA.xml b/data/38/A8/E1/38A8E11EE37751AAECC369B60D87BDEA.xml new file mode 100644 index 00000000000..3c48f8c0325 --- /dev/null +++ b/data/38/A8/E1/38A8E11EE37751AAECC369B60D87BDEA.xml @@ -0,0 +1,90 @@ + + + +Checklist of British and Irish Hymenoptera - Braconidae + + + +Author + +Broad, Gavin R. + + + +Author + +Shaw, Mark R. + + + +Author + +Godfray, H. Charles J. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8151 +8151 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8151 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8151 +1314-2828-4-8151 + + + + +Perilitus rutilus (Nees, 1811) + + + + +Bracon rutilus +Nees, 1811 + + +luteus +Herrich-Schaeffer +, 1838 + + +ruralis +Herrich-Schaeffer +, 1838 + + +strenuus +Marshall, 1887; synonymy by +Haeselbarth (1999) + + +pyri +(Viereck, 1917, +Dinocampus +) + + +tuberculus +Zaykov, 1981; synonymy by +Haeselbarth (1999) + + + +Distribution +England, Ireland + + + \ No newline at end of file diff --git a/data/38/A8/F3/38A8F3F4F23C2D97E10592C92E6F7AC2.xml b/data/38/A8/F3/38A8F3F4F23C2D97E10592C92E6F7AC2.xml new file mode 100644 index 00000000000..8c6cdb93289 --- /dev/null +++ b/data/38/A8/F3/38A8F3F4F23C2D97E10592C92E6F7AC2.xml @@ -0,0 +1,78 @@ + + + +Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea + + + +Author + +Dale-Skey, Natalie + + + +Author + +Askew, Richard R. + + + +Author + +Noyes, John S. + + + +Author + +Livermore, Laurence + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8013 +8013 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8013 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8013 +1314-2828--8013 + + + + +Gyrinophagus aper (Walker, 1839) + + + + +Pteromalus aper +Walker, 1839 + + +marginatus +(Thomson, 1878, +Isocyrtus +) + + + + \ No newline at end of file diff --git a/data/38/A9/8D/38A98D0B43D8C3534FC6C483C42A7A89.xml b/data/38/A9/8D/38A98D0B43D8C3534FC6C483C42A7A89.xml new file mode 100644 index 00000000000..d5f3faffcf0 --- /dev/null +++ b/data/38/A9/8D/38A98D0B43D8C3534FC6C483C42A7A89.xml @@ -0,0 +1,46 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828-4-9042 + + + + +Diaparsis (Diaparsis) multiplicator Aubert, 1969 + + + +Distribution +England + + + \ No newline at end of file diff --git a/data/38/A9/DC/38A9DC92769DE0C403527FD189F4997C.xml b/data/38/A9/DC/38A9DC92769DE0C403527FD189F4997C.xml new file mode 100644 index 00000000000..c103321e159 --- /dev/null +++ b/data/38/A9/DC/38A9DC92769DE0C403527FD189F4997C.xml @@ -0,0 +1,132 @@ + + + +Order Soricomorpha + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +220 +311 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Mogera wogura +subsp. +wogura +Temminck 1842 + + + + + + + +Mogera wogura +subsp. +wogura +Temminck 1842 + +, +in: Siebold, Fauna Japonica, 1 (Mamm.), 1: 19 + +. + + + + +Type Locality: + +Japan +; restricted to Yokohama, Honshu by + +Thomas (1905 +b +) + +, but believed to have come from W or S Kyushu by +Abe (1995) + +. + + + + +Synonyms: + +Mogera wogura +subsp. +aquilonaris +Kishida 1950 + +; + +Mogera wogura +subsp. +gracilis +Kishida 1936 + +; + +Mogera wogura +subsp. +kanai +Thomas 1905 + +; + +Mogera wogura +subsp. +kiusiuana +Kuroda 1940 + +; + +Mogera wogura +subsp. +kobeae +Thomas 1905 + +; + +Mogera wogura +subsp. +moogura +Temminck 1842 + +. + + + + \ No newline at end of file diff --git a/data/38/A9/E5/38A9E59B697BEEC16B4EF9281DFF49F3.xml b/data/38/A9/E5/38A9E59B697BEEC16B4EF9281DFF49F3.xml new file mode 100644 index 00000000000..0b6db69ef13 --- /dev/null +++ b/data/38/A9/E5/38A9E59B697BEEC16B4EF9281DFF49F3.xml @@ -0,0 +1,235 @@ + + + +New records of Ichneumonidae (Hymenoptera) for the Italian fauna + + + +Author + +Di Giovanni, Filippo + + + +Author + +Reshchikov, Alexey + + + +Author + +Riedel, Matthias + + + +Author + +Diller, Erich + + + +Author + +Schwarz, Martin + +text + + +Biodiversity Data Journal + + +2015 + +3 + + +5057 +5057 + + + + +http://dx.doi.org/10.3897/BDJ.3.e5057 + +journal article +http://dx.doi.org/10.3897/BDJ.3.e5057 +1314-2828--5057 + + + + +Heresiarches eudoxius (Wesmael, 1845) + + + +Materials + + +Type status: +Other material +. Occurrence: recordedBy: +F. Di Giovanni +; individualCount: +1 +; sex: +male +; Location: country: +Italy +; stateProvince: Friuli-Venezia Giulia; verbatimLocality: Udine, Palazzolo dello Stella, Nogali Braide, bosco Brussa; verbatimElevation: +0 m +; verbatimLatitude: +45°45'54.05"N +; verbatimLongitude: +13°04'52.15"E +; Identification: identifiedBy: +M. Riedel +; dateIdentified: 2014; Event: samplingProtocol: +Malaise trap +; eventDate: +08-18.V.2013 +; Record Level: institutionCode: +MZUR + + +Type status: +Other material +. Occurrence: recordedBy: +F. Di Giovanni +; individualCount: +1 +; sex: +male +; Location: country: +Italy +; stateProvince: Friuli-Venezia Giulia; verbatimLocality: Udine, Porpetto, bosco Sgobitta; verbatimElevation: +15 m +; verbatimLatitude: +45°51'13.54"N +; verbatimLongitude: +13°11'44.78"E +; Identification: identifiedBy: +M. Riedel +; dateIdentified: 2014; Event: samplingProtocol: +Malaise trap +; eventDate: +08-18.V.2013 +; Record Level: institutionCode: +MZUR + + +Type status: +Other material +. Occurrence: recordedBy: +F. Di Giovanni +; individualCount: +1 +; sex: +male +; Location: country: +Italy +; stateProvince: Veneto; verbatimLocality: Treviso, Cessalto, Santa Maria di Campagna, bosco San Marco; verbatimElevation: +0 m +; verbatimLatitude: +45°42'21.22"N +; verbatimLongitude: +12°34'42.45"E +; Identification: identifiedBy: +M. Riedel +; dateIdentified: 2014; Event: samplingProtocol: +Malaise trap +; eventDate: +10-22.VI.2013 +; Record Level: institutionCode: +MZUR + + +Type status: +Other material +. Occurrence: recordedBy: +F. Di Giovanni +; individualCount: +7 +; sex: +males +; Location: country: +Italy +; stateProvince: Friuli-Venezia Giulia; verbatimLocality: Udine, Palazzolo dello Stella, Nogali Braide, bosco Brussa; verbatimElevation: +0 m +; verbatimLatitude: +45°45'54.05"N +; verbatimLongitude: +13°04'52.15"E +; Identification: identifiedBy: +M. Riedel +; dateIdentified: 2014; Event: samplingProtocol: +Malaise trap +; eventDate: +21.VII-03.VIII.2013 +; Record Level: institutionCode: +MZUR + + +Type status: +Other material +. Occurrence: recordedBy: +F. Di Giovanni +; individualCount: +1 +; sex: +male +; Location: country: +Italy +; stateProvince: Veneto; verbatimLocality: Treviso, Gaiarine, Francenigo, bosco Crasere; verbatimElevation: +15 m +; verbatimLatitude: +45°54'01.85"N +; verbatimLongitude: +12°30'00.86"E +; Identification: identifiedBy: +M. Riedel +; dateIdentified: 2014; Event: samplingProtocol: +Malaise trap +; eventDate: +23.VII-05.VIII.2013 +; Record Level: institutionCode: +MZUR + + +Type status: +Other material +. Occurrence: recordedBy: +F. Di Giovanni +; individualCount: +7 +; sex: +males +; Location: country: +Italy +; stateProvince: Veneto; verbatimLocality: Treviso, Cessalto, Santa Maria di Campagna, bosco San Marco; verbatimElevation: +0 m +; verbatimLatitude: +45°42'21.22"N +; verbatimLongitude: +12°34'42.45"E +; Identification: identifiedBy: +M. Riedel +; dateIdentified: 2014; Event: samplingProtocol: +Malaise trap +; eventDate: +23.VII-05.VIII.2013 +; Record Level: institutionCode: +MZUR + + + + +Distribution +Europe. + + +Notes +New for Italy. + + + \ No newline at end of file diff --git a/data/38/AA/8E/38AA8E5E80E65A7EB0BEB3499FE66013.xml b/data/38/AA/8E/38AA8E5E80E65A7EB0BEB3499FE66013.xml new file mode 100644 index 00000000000..0b7e0a681c0 --- /dev/null +++ b/data/38/AA/8E/38AA8E5E80E65A7EB0BEB3499FE66013.xml @@ -0,0 +1,85 @@ + + + +Distribution patterns of Chinese Cixiidae (Hemiptera, Fulgoroidea), highlight their high endemic diversity + + + +Author + +Luo, Yang +Key Laboratory of Plant Protection Resources and Pest Management, Ministry of Education, Entomological Museum, College of Plant Protection, Northwest A & F University, Yangling, Shaanxi 712100, China, Yangling, China + + + +Author + +Bourgoin, Thierry +https://orcid.org/0000-0001-9277-2478 +Institut de Systematique, Evolution, Biodiversite, ISYEB-UMR 7205, MNHN-CNRS-Sorbonne Universite-EPHE-Univ. Antilles, Museum national d'Histoire naturelle, CP 50, 57 rue Cuvier, F- 75005, Paris, France +thierry.bourgoin@mnhn.fr + + + +Author + +Zhang, Jia-Lin +Key Laboratory of Plant Protection Resources and Pest Management, Ministry of Education, Entomological Museum, College of Plant Protection, Northwest A & F University, Yangling, Shaanxi 712100, China, Yangling, China + + + +Author + +Feng, Ji-Nian +Key Laboratory of Plant Protection Resources and Pest Management, Ministry of Education, Entomological Museum, College of Plant Protection, Northwest A & F University, Yangling, Shaanxi 712100, China, Yangling, China +jinianf@nwsuaf.edu.cn + +text + + +Biodiversity Data Journal + + +2022 + +2022-01-24 + + +10 + + +75303 +75303 + + + + +http://dx.doi.org/10.3897/BDJ.10.e75303 + +journal article +http://dx.doi.org/10.3897/BDJ.10.e75303 +1314-2828-10-e75303 +07802C19F192544C9F561556F25CA5C4 + + + + +Mundopa kotoshonis Matsumura, 1914 + + + + +Mundopa kotoshonis +Matsumura, 1914: 430.| Tsaur et al., 1991a: 76. + + + +Distribution + +China: Taiwan ( +Tsaur et al. 1991a +). + + + + \ No newline at end of file diff --git a/data/38/AB/E9/38ABE936931FB5E4E6091134AADFA087.xml b/data/38/AB/E9/38ABE936931FB5E4E6091134AADFA087.xml new file mode 100644 index 00000000000..e1891bb9af8 --- /dev/null +++ b/data/38/AB/E9/38ABE936931FB5E4E6091134AADFA087.xml @@ -0,0 +1,168 @@ + + + +A monograph of the Xyleborini (Coleoptera, Curculionidae, Scolytinae) of the Indochinese Peninsula (except Malaysia) and China + + + +Author + +Smith, Sarah M. +Department of Entomology, Michigan State University, 288 Farm Lane, East Lansing, Michigan 48824, USA +https://orcid.org/0000-0002-5173-3736 +camptocerus@gmail.com + + + +Author + +Beaver, Roger A. +161 / 2 Mu 5, Soi Wat Pranon, T. Donkaew, A. Maerim, Chiangmai 50180, Thailand + + + +Author + +Cognato, Anthony I. +Department of Entomology, Michigan State University, 288 Farm Lane, East Lansing, Michigan 48824, USA + +text + + +ZooKeys + + +2020 + +983 + + +1 +442 + + + + +http://dx.doi.org/10.3897/zookeys.983.52630 + +journal article +http://dx.doi.org/10.3897/zookeys.983.52630 +1313-2970-983-1 +7DED4CE2934C4539945F758930C927F9 +C890C7FD4B2D57A8B1A062305ED42D53 + + + + +Euwallacea destruens (Blandford, 1896) +Fig. 54C, D, J + + + + +Xyleborus destruens +Blandford, 1896b: 221. + + +Euwallacea destruens +(Blandford): +Wood 1989 +: 173. + + +Xyleborus barbatus +Hagedorn, 1910a: 11. Synonymy: +Bright and Skidmore 1997 +: 4, 149. + + +Xyleborus barbatulus +Schedl, 1934b: 86. Synonymy: +Bright and Skidmore 1997 +: 4, 149. + + +Xyleborus pseudobarbatus +Schedl, 1942a: 193. Synonymy: +Wood 1989 +: 173. + + +Xyleborus nandarivatus +Schedl, 1950a: 53. Synonymy: +Wood 1989 +: 173. + + +Xyleborus procerrimus +Schedl, 1969a: 214. Synonymy: +Hulcr and Cognato 2013 +: 92. + + + +Type material. + +Syntype + +Xyleborus barbatus + +(SDEI). +Syntype + +Xyleborus destruens + +(NHMUK). + + + +Diagnosis. + +3.9-4.6 mm long (mean = 4.19 mm; n = 6); 2.54-2.79 +x +as long as wide. This species is distinguished by its large body size and elongate form; protibiae distinctly triangular with 4-6 denticles in the apical 1/2; declivity commencing at posterior 1/3, steeper than in + +E. gravelyi + +, and usually appearing concave in lateral view. + + + +Similar species. + + +Euwallacea gravelyi + +. + + + +Distribution. +From the Andaman Islands, and Southwest China, through Southeast Asia to Malaysia, Indonesia and the Philippines to New Guinea, Australia and the Pacific islands. Recorded in the study region from China (Yunnan), India (Andaman Is), Taiwan, Thailand, Vietnam. + + +Host plants. + +Polyphagous ( +Browne 1961b +). + + + +Remarks. + +The species is an important pest of teak ( + +Tectona grandis + +) ( +Lamiaceae +) in Java and other areas where there is only a short or no dry season ( +Browne 1968a +; +Kalshoven 1962 +). + + + + \ No newline at end of file diff --git a/data/38/AB/EA/38ABEA465BBB30FFDD22C6BAC67251E3.xml b/data/38/AB/EA/38ABEA465BBB30FFDD22C6BAC67251E3.xml new file mode 100644 index 00000000000..1b9ee1214f6 --- /dev/null +++ b/data/38/AB/EA/38ABEA465BBB30FFDD22C6BAC67251E3.xml @@ -0,0 +1,45 @@ + + + +Description de formicides éthiopiens nouveaux ou peu connus. V. + + + +Author + +Santschi, F. + +text + + +Bulletin et Annales de la Societe Entomologique de Belge + + +1930 + +70 + + +49 +77 + + + + +http://antbase.org/ants/publications/3641/3641.pdf + +journal article +3641 + + + + +Euponera (Trachymesopus) darwini For. v. africana +For. + + + +Soudan francais: Koulouba (Andrieu), 2 [[ queen ]], juin 1928. + + + \ No newline at end of file diff --git a/data/38/AC/18/38AC188305F75267B526A81A2FC43028.xml b/data/38/AC/18/38AC188305F75267B526A81A2FC43028.xml new file mode 100644 index 00000000000..6bf6cf472e2 --- /dev/null +++ b/data/38/AC/18/38AC188305F75267B526A81A2FC43028.xml @@ -0,0 +1,95 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Sphinx elpenor +[ +spec. nov. +] + + + + +S. alis integris viridi purpureoque variis: inferioribus basi atris. +Fn. svec. +811. + +Mouff. ins. +183. +Raj. ins. +145. +n. +2. +Pet. gaz. t. +40. +f. +11. 12. 17. +Alb. ins. t. +9. +f. +13. +Merian. ins. +2. +t. +33. +f. +73. +Frisch. ins. +12. +t. +1. +Roes. ins. +1. +phal. +1. +t. +4. +De Geer. ins. +1. +t. +9. +f. +8. 9. + +Wilk. pap. +11. +t. +1. +B. +7. + + + + +Habitat in +Epilobio, Impatiente, Vite. + + + + \ No newline at end of file diff --git a/data/38/AE/DD/38AEDDEB80C488E5BA4A982F58E80F7A.xml b/data/38/AE/DD/38AEDDEB80C488E5BA4A982F58E80F7A.xml new file mode 100644 index 00000000000..d9a399e4f0b --- /dev/null +++ b/data/38/AE/DD/38AEDDEB80C488E5BA4A982F58E80F7A.xml @@ -0,0 +1,84 @@ + + + +A nomenclator of extant and fossil taxa of the Melanopsidae (Gastropoda, Cerithioidea) + + + +Author + +Neubauer, Thomas A. +https://orcid.org/0000-0002-1398-9941 +Geological-Paleontological Department, Natural History Museum Vienna, 1010 Vienna, Austria +thomas.neubauer@nhm-wien.ac.at + +text + + +ZooKeys + + +2016 + +2016-07-05 + + +602 + + +1 +358 + + + + +http://dx.doi.org/10.3897/zookeys.602.8136 + +journal article +http://dx.doi.org/10.3897/zookeys.602.8136 +1313-2970-602-1 +65EFA27673454AC69B78DBE7E98D6103 +FFA86D39FFE2FFF3FF8AFFEBC209FFDE +126863 + + + + +† +Melanopsis fallax Pantanelli, 1886 + + + +Original source. + +Pantanelli 1886a +: 64 or 1886b: 67, pl. 3, figs 12-13 (precedence not established). + + + +Type horizon. +Messinian, late Miocene. + + +Type locality. + +"Sterza" +( +Capellini 1873 +: 550) [near Lajatico], Italy. + + + +Remarks. + +Introduced for the record of + +Melanopsis acicularis + +sensu Capellini, 1873, non +Ferussac +, 1823. + + + + \ No newline at end of file diff --git a/data/38/AF/1C/38AF1C24E9C5A215C3CF71FE3B74AADC.xml b/data/38/AF/1C/38AF1C24E9C5A215C3CF71FE3B74AADC.xml new file mode 100644 index 00000000000..f07eee2b46b --- /dev/null +++ b/data/38/AF/1C/38AF1C24E9C5A215C3CF71FE3B74AADC.xml @@ -0,0 +1,139 @@ + + + +Order Rodentia - Family Muridae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 2 + + + +1189 +1531 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316535 + + + + + +Dipodillus (Petteromys) harwoodi +Thomas 1901 + + + + + + + +Dipodillus (Petteromys) harwoodi +Thomas 1901 + +, +Ann. Mag. Nat. Hist., ser. 7, 8: 275 + +. + + + + +Type Locality: + +Kenya +, Lake Naivasha. + + + + + +Vernacular Names: +Harwood's Dipodil +. + + + + +Synonyms: + +Dipodillus (Petteromys) luteus +Dollman 1914 + +. + + + + +Distribution: +Kenya +and +Tanzania +(see F. + +Petter, 1975 +b + +, and +Swynnerton and Hayman, 1951 +). + + + + +Conservation: +IUCN +– Lower Risk (lc) as + +Gerbillus harwoodi + +. + + + + +Discussion: +Subgenus + +Petteromys + +. Defined as a distinct species by +Roche (1975) +. The relationship between this species and + +D. bottai + +requires resolution; see comments under account of + +D. bottai + +and the discussion by +Pavlinov et al. (1990) +. + + + + \ No newline at end of file diff --git a/data/38/AF/1E/38AF1E26A0D5F15B6FF7797B25444022.xml b/data/38/AF/1E/38AF1E26A0D5F15B6FF7797B25444022.xml new file mode 100644 index 00000000000..454b2712b37 --- /dev/null +++ b/data/38/AF/1E/38AF1E26A0D5F15B6FF7797B25444022.xml @@ -0,0 +1,214 @@ + + + +Order Rodentia - Family Geomyidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 2 + + + +859 +870 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316535 + + + + + +Cratogeomys tylorhinus +(Merriam 1895) + + + + + + + +Cratogeomys tylorhinus +(Merriam 1895) + +, +N. Amer. Fauna, 8: 167 + +. + + + + +Type Locality: + +Mexico +, +Hidalgo +, Tula, +6,800 ft. +( + +2,073 m + +). + + + + + +Vernacular Names: +Naked-nosed Pocket Gopher +. + + + + +Subspecies: +: + + +Subspecies + +Cratogeomys tylorhinus +subsp. +tylorhinus +(Merriam 1895) + + + +Subspecies + +Cratogeomys tylorhinus +subsp. +angustirostris +(Merriam 1903) + + + +Subspecies + +Cratogeomys tylorhinus +subsp. +atratus +Russell 1953 + + + +Subspecies + +Cratogeomys tylorhinus +subsp. +brevirostris +Russell 1968 + + + +Subspecies + +Cratogeomys tylorhinus +subsp. +planiceps +(Merriam 1895) + + + +Subspecies + +Cratogeomys tylorhinus +subsp. +zodius +Russell 1953 + + + + + +Distribution: +Distrito Federal +and +Hidalgo +to C +Jalisco +( +Mexico +). + + + + +Conservation: +IUCN +– Lower Risk (nt) as + +Pappogeomys tylorhinus + +. + + + + +Discussion: +Included in the + +gymnurus + +species-group by + +Russell (1968 +b +) + +and probably same species as + +fumosus +( +Demastes et al., 2002 +) + +. As currently understood, however, + +tylorhinus + +is polytypic; subspecies reviewed by + +Russell (1968 +b +) + +. Reviewed by + +Cervantes et al. (1993 +a + +, Mammalian Species No. 433) as + +Pappogeomys tylorhinus + +. + + + + \ No newline at end of file diff --git a/data/38/AF/89/38AF89B9CAC896657DF659D79B90F1F8.xml b/data/38/AF/89/38AF89B9CAC896657DF659D79B90F1F8.xml new file mode 100644 index 00000000000..65aa6c319d2 --- /dev/null +++ b/data/38/AF/89/38AF89B9CAC896657DF659D79B90F1F8.xml @@ -0,0 +1,112 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part G) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +529 +556 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Gentiana bavarica +Linnaeus + +, + +Species Plantarum +1 + +: 229. 1753 + + +. + + + +"Habitat in alpibus Helvetiae, Bavaria." RCN: 1870. + + +Type not designated. + + + +Original material: + +Herb. Linn. No. 112.15 ( +S +) + +; + +Herb. Clifford: 81, + +Gentiana + +6 ( +BM +) + +; [icon] in Camerarius, Hort. Med. Phil.: 65, t. 15 f. 2. 1588. + + + + +Current name: + +Gentiana bavarica +L. + +( +Gentianaceae +). + + + + +Note: +Ho & Liu (in +Worldw. Monogr. +Gentiana +: 270. 2001) indicate what is evidently a Clifford sheet as +holotype +(with a specimen in S as +"type" +). The Clifford material must therefore be intended as a +lectotype +, but the absence of "designated here" (Art. 7.11) appears to make this an ineffective type choice. + + + + \ No newline at end of file diff --git a/data/38/AF/95/38AF95C030E6C01A07987DE6C83A5F7E.xml b/data/38/AF/95/38AF95C030E6C01A07987DE6C83A5F7E.xml new file mode 100644 index 00000000000..585cb3de343 --- /dev/null +++ b/data/38/AF/95/38AF95C030E6C01A07987DE6C83A5F7E.xml @@ -0,0 +1,98 @@ + + + +New records of Agromyzidae (Diptera) from Switzerland and an updated checklist + + + +Author + +erny, Milos + + + +Author + +Baechli, Gerhard + +text + + +Alpine Entomology + + +2018 + +2 + + +115 +137 + + + + +http://dx.doi.org/10.3897/alpento.2.28973 + +journal article +http://dx.doi.org/10.3897/alpento.2.28973 +2535-0889--115 +C7E181A32C884D14B2A67D49ECBB2CDB + + + + +Phytomyza mylini Hering, 1954 + + + +Material examined. + +VS: Visp [ +46°18'N +, +07°53'E +, 670m a.s.l.], 1 ♂, 2000, P. Duelli leg. + + + +Distribution. +Europe: Czech Republic, Finland, France, Germany, L + + +a + +tvia, Lithuania, Poland ( + +Kahanpaeae +2014 + +, +Karpa 2008 +, +Withers 2014 +). First record from Switzerland. + + + +Biology. + +Host plants +Carum +, +Cicuta +, +Daucus +, +Ligusticum +, +Selinum +, +Seseli +, +Silaum +. + + + + \ No newline at end of file diff --git a/data/38/AF/A1/38AFA12241CCC0945E07493FF2F40709.xml b/data/38/AF/A1/38AFA12241CCC0945E07493FF2F40709.xml new file mode 100644 index 00000000000..1dd2773dec9 --- /dev/null +++ b/data/38/AF/A1/38AFA12241CCC0945E07493FF2F40709.xml @@ -0,0 +1,128 @@ + + + +Order Chiroptera - Family Vespertilionidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +451 +529 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Chalinolobus neocaledonicus +Revilliod 1914 + + + + + + + +Chalinolobus neocaledonicus +Revilliod 1914 + +, + +in: Sarasin and Roux, +Nova Caledonia +, A. Zool.: 355 + + +. + + + + +Type Locality: + +New Caledonia +, Canala. + + + + + +Vernacular Names: + +New Caledonia +Wattled Bat + +. + + + + +Distribution: +New Caledonia +. + + + + +Conservation: +IUCN +2003 and +IUCN +/ +SSC +Action Plan (2001) – Endangered. + + + + +Discussion: +Often treated as a subspecies of + +gouldii + +(e.g., + +Koopman, 1971 +a + +, 1994; +Tidemann, 1986 +), but evidence for synonymy is weak; I follow Flannery (1995 +b +) in provisionally recognizing + +neocaledonicus + +as distinct pending further study. + + + + \ No newline at end of file diff --git a/data/38/AF/DA/38AFDA44F1B23C635ACF71FD5BF5ED03.xml b/data/38/AF/DA/38AFDA44F1B23C635ACF71FD5BF5ED03.xml new file mode 100644 index 00000000000..87d53bbcc75 --- /dev/null +++ b/data/38/AF/DA/38AFDA44F1B23C635ACF71FD5BF5ED03.xml @@ -0,0 +1,100 @@ + + + +Review of the ant genus Nesomyrmex (Hymenoptera: Formicidae: Myrmicinae) in southern Africa. + + + +Author + +Mbanyana, N. + + + +Author + +Robertson, H. G. + +text + + +African Natural History + + +2008 + +4 + + +35 +55 + + + + +http://antbase.org/ants/publications/23052/23052.pdf + +journal article +23052 + + + + + +Nesomyrmex denticulatus( +Mayr, 1901 +) + +Fig. 2d -f + + + + + +Leptothorax denticulatus +Mayr, 1901: 5 + +. For type information and synonyms see +Bolton (1982) +. + + + +Description of worker +HL 0.828-0.921, HW 0.629-0.757, HW1 0.679-0.795, CI 73-84, SL 0.462-0.580, SI 73-77, PW 0.482-0.590, ML 0.895-1.087, EL 0.177-0.216, EI 26-29 (5 of 61 measured). + +Description as in +Bolton (1982) +, but with the following differences: mandibles are described as finely shagreened to virtually smooth but in the material that we observed mandibles can also have fine longitudinal striations. + + + +Diagnosis + +Nesomyrmex denticulatus +looks similar to +N. stramineus +in that in both the petiolar node bears denticles from which hairs arise. It is distinguished from the latter species by its larger size (HW 0.629-0.757 versus 0.502-0.525), welldeveloped subpetiolar process, which consists of a tooth anteriorly followed by a long cuticular flange; and larger eyes (EI 26-29 versus 24-27). + + + +Biology + +Usually nests in cavities of branches on trees and bushes that were previously excavated by wood-boring beetles or termites. Nests have also been found in cavities at the base of old Protea inflorences that were previously excavated by beetle or lepidopteran larvae. It is found in vegetation of the Western Cape and Eastern Cape that has a woody +component +, including late succession Fynbos, Succulent Karoo that has large bushes, Southern Afrotemperate Forest(mainly along edges) and possibly also Albany Thicket. + + + + +Material +examined + + +South Africa: Eastern Cape: Grahamstown, 33°18'S 26°32'E, in cavity of dead branch, 05 April 1996, L.X. Silberbauer & L. Bennet, SAM-HYM-C009736; Western Cape: Ouberg SePas, 33°42'0"S 20°15'0"E, Succulent Karoo on rocky slope, 28 February 1999, H.G. Robertson, SAM-HYM-C013042; Cape of Good Hope Nature Reserve, Olifantsbos near Skaife Centre, 34°15.76'S 18°23.13'E,20 m alt., Strandveld Mountain Fynbos ecotone: dense bush, white pitfall, 23 Feb -23 Mar 1998, M.H. Troskie, SAM-HYM-C017281; Cape of Good Hope Nature Reserve, Olifantsbos near Skaife Centre, 34°15.76'S 18°23.13'E, 20 m alt., Strandveld Mountain Fynbos ecotone: dense bush, yellow pitfall, 23 Feb -23 Mar 1998, M.H. Troskie, SAM-HYM-C017282; Cape Peninsula National Park, Cape of Good Hope sec., near Klaasjagersberg, 1A; 34°14'06"S 18°23'36"E, Regenerated Mesic Mountain Fynbos on flat land after alien clearing using bulldozer (Treatment 1A), pitfall trap, 25 Feb -27 Mar 1999, F. Parker, SAM-HYM-C 017283; Cape Peninsula National Park, Silvermine, 34°05.05'S 18°25.14'E, nest in hollowed out baseofdead Protea repens inflorescence, Mesic Mountain Fynbos, 14 May 1998, G. Eick & H.G. Robertson, SAM-HYM-C015012; Kleinmond, 34°20'0"S 18°59'0"E, 30 September 2000, H.G. Robertson, SAM-HYM-C017822; Brandfontein Reserve, 34°46'S 19°52'E, in cavity of old Protea suzannae inflorescence, Mesic Mountain Fynbos on sandstone,15 August 1992, H.G. Robertson, SAM-HYM-C007230; At foot of Duivelsbos, Marloth Nature Reserve, 33°59'50"S 20°27'50"E, forest along stream, with tiny +Monomorium +sp. in the same branch, nest in dead branch on tree, on fringe of indigenous evergreen, 09 October 1994, H.G. Robertson, SAM-HYM-C 007519; Fernkloof Nature Reserve, 34°24'S 19°17'E, 14-15 Nov 1992, H.G. Robertson, SAM-HYM-C006428; Brenton-on-sea, 34°04'00"S 23°01'00"E, Fynbos site: nest in cavity of 1.5 cm thick dead branch above ground, 01-07 December1996, H.G.Robertson,SAM-HYM-C009434;Cape Peninsula National Park, Silvermine, 34°05.05'S 18°25.14'E, Nest in hollowed out base of dead Protea repens inflorescence, Mesic Mountain Fynbos, 14 May 1998, H.G. Robertson & G. Eick, SAM-HYM-C015006. + + + + \ No newline at end of file diff --git a/data/38/AF/F5/38AFF54DACF6AA7F892AD5F490AEA068.xml b/data/38/AF/F5/38AFF54DACF6AA7F892AD5F490AEA068.xml new file mode 100644 index 00000000000..61c16283055 --- /dev/null +++ b/data/38/AF/F5/38AFF54DACF6AA7F892AD5F490AEA068.xml @@ -0,0 +1,60 @@ + + + +Brazilian Trichoptera Checklist II + + + +Author + +Paprocki, Henrique + + + +Author + +Franca, Diogo + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1557 +1557 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1557 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1557 +1314-2828--1557 + + + + +Chimarra (Chimarrita) camura Blahnik, 1997 + + + +Distribution +Rio de Janeiro, Sao Paulo + + +Notes + +Blahnik 1997 +, +Blahnik et al. 2004 + + + + \ No newline at end of file diff --git a/data/38/B0/5C/38B05C532EE5DAFA90A6103C3FBD0CB9.xml b/data/38/B0/5C/38B05C532EE5DAFA90A6103C3FBD0CB9.xml new file mode 100644 index 00000000000..abf694e97aa --- /dev/null +++ b/data/38/B0/5C/38B05C532EE5DAFA90A6103C3FBD0CB9.xml @@ -0,0 +1,109 @@ + + + +The Doryctinae (Braconidae) of Costa Rica: genera and species of the tribe Heterospilini + + + +Author + +Marsh, Paul M. + + + +Author + +Wild, Alexander L. + + + +Author + +Whitfield, James B. + +text + + +ZooKeys + + +2013 + +347 + + +1 +474 + + + + +http://dx.doi.org/10.3897/zookeys.347.6002 + +journal article +http://dx.doi.org/10.3897/zookeys.347.6002 +1313-2970-347-1 +52232D18DD784A84882CACA428B4A9D2 +52232D18DD784A84882CACA428B4A9D2 + + + + +Heterospilus bribri Marsh +sp. n. +Figure 21 + + + +Female. + +Body size: 2.5-3.5 mm. Color: head with vertex and frons brown, face and eye orbits yellow; scape yellow without lateral longitudinal brown stripe, flagellum brown; +mesosoma +brown, pronotum often light brown; metasomal tergum 1 dark brown, tergum 2 brown to honey yellow, terga 3-6 dark brown basally, yellow apically, tergum 7 yellow; wing veins brown, stigma bicolored brown with yellow apex; legs yellow. Head: vertex transversely costate; frons transversely costate; face smooth; temple in dorsal view narrow, width less than 1/2 eye width; malar space greater than 1/4 eye height; ocell-ocular distance about 2.5 times diameter of lateral ocellus; 26-31 flagellomeres. Mesosoma: mesoscutal lobes granulate; notauli scrobiculate, meeting at scutellum in triangular costate-rugose area; scutellum granulate; prescutellar furrow with 3 cross carinae; mesopleuron granulate; precoxal sulcus weakly scrobiculate or smooth, shorter than mesopleuron; venter granulate; propodeum with basal median areas margined, granulate, basal median carina present, areola distinctly margined, areolar area rugose, lateral areas entirely granulate. Wings: fore wing vein r shorter than vein 3RSa, vein 1cu-a interstitial or very slightly beyond vein 1M; hind wing vein SC+R present, vein M+CU shorter than vein 1M. Metasoma: first tergum costate, apical width less than length; second tergum costate-granulate, width about 4 times length; anterior transverse groove present, sinuate; posterior transverse groove weakly indicated or absent; third tergum entirely granulate; terga 4-7 granulate at base, smooth apically; ovipositor as long as metasoma. + + + +Holotype female. +Top label (white, printed) - COSTA RICA: [;] Puntar. Golfo Dulce [;] 24km W Piedras Blancas [;] 200m, vi-viii 1989 [;] Hanson; second label (red, partially printed and hand written) - HOLOTYPE [;] Heterospilus [;] bribri [;] P. Marsh. Deposited in ESUW. + + +Paratypes. + +1 + +, Costa Rica: Puntarenas, [;] R.F. Golfo Dulce, 5km. [;] W. Piedras Blancas, 100m [;] +xi-xii +.1991, P. Hanson, [;] Malaise nr. second growth (ESUW). 4 ♀♀, COSTA RICA-Heredia Prov. [;] La Selva Biological Station [;] +10°26'N +, +84°01'W +, 100m [;] Canopy fogging 19, 31 and 32 [;] 8.x.1994, 2.xi.1994 and 3.xi.1994 [;] Project ALAS (FCK19, 31 and 32) (ESUW). 1 ♀, Costa Rica: Heredia [;] 3km. S. Puerto Viejo [;] OTS, La Selva, 100m [;] xi.1992, P. Hanson (ESUW). 1 ♀, Costa Rica: Guanacaste, ACT [;] Bagaces, P.N. Palo Verde, 212m [;] Sec. Palo Verde, Cerro Guayacan [;] 13. +ix- +13.x.1999, I. Jimenez, Malaise [;] L.N. 259350-389600 #53499 (ESUW). 2 ♀♀, top label - Costa Rica: Guanacaste [;] Santa Rosa Natl. Park [;] 300m, ex. Malaise trap [;] Site #: blank [;] Dates: 14. +viii- +6.ix.1986 and 7-28.xii.1985 [;] I.D. Gauld & D. Janzen; second label - [SE] Bosque San Emilio [;] 50yr old deciduous forest [;] [C] more or less fully [;] shaded as possible (ESUW). 1 ♀, top label - Costa Rica: Guanacaste [;] Santa Rosa Natl. Park [;] 300m, ex. Malaise trap [;] Site #: 10 [;] Dates: 26. +x- +16.xi.1985 [;] I.D. Gauld & D. Janzen; second label - [BH] Bosque Humedo [;] mature evergreen dry forest [;] [C] more or less fully [;] shaded as possible (ESUW). 1 ♀, Costa Rica: Guanacaste [;] Santa Rosa National Pk. [;] 300m, Malaise SE-6-C [;] Bosque San Emilio, [;] deciduous forest [;] 50yr. old, Ian Gauld [;] 5.vii.1986, full shade (ESUW). 2 ♀♀, COSTA RICA: Puntarenas [;] RF Golfo Dulce, el 200m [;] 24km W Piedras Blancas [;] P. Hanson vii and ix.1992 (TAMU). 1 ♀, COSTA RICA, Puntar. [;] Golfo Dulce, 3km [;] SW. Rincon, 10m [;] III-VI 1990, Hanson (MICR). 1 ♀, COSTA RICA, Puntar. [;] Golfo Dulce, 24km W. [;] PiedrasBlancas, 200m [;] XII.89-III.90 Hanson (MICR). 1 ♀, Sirena, Osa Pen. [;] VII.77 Cos. Rica [;] D. H. Janzen (AEIC). 5 ♀♀, S.RosaPark, Guan. [;] C. Rica. 25 Jun 77, 15 Jun 77, 16 Nov. 77, 14 Nov 77 and 20 Nov 77 [;] D.H. Janzen [;] Riparian and Dry Hill (AEIC). + + + +Comments. +This species is distinguished by the 3 cross carinae in the prescutellar furrow and the granulate metasomal terga. + + +Etymology. +Named for the Bribri, an indigenous people group of Costa Rica. + + +Figure 21. +Heterospilus bribri +Marsh, sp. n.: +A-C +paratype +D-E +holotype. + + + + + \ No newline at end of file diff --git a/data/38/B0/8E/38B08EB161945902A8E367EC98AA0AC7.xml b/data/38/B0/8E/38B08EB161945902A8E367EC98AA0AC7.xml new file mode 100644 index 00000000000..1198ec39f8b --- /dev/null +++ b/data/38/B0/8E/38B08EB161945902A8E367EC98AA0AC7.xml @@ -0,0 +1,239 @@ + + + +Six new species of the orb-weaver spider genus Araneus Clerck, 1757 (Araneae, Araneidae) and a redescription of A. colubrinus Song & Zhu, 1992 from Fanjingshan National Nature Reserve, Guizhou, China + + + +Author + +Mi, Xiaoqi +https://orcid.org/0000-0003-1744-3855 +College of Agriculture and Forestry Engineering and Planning, Guizhou Provincial Key Laboratory of Biodiversity Conservation and Utilization in the Fanjing Mountain Region, Tongren University, Tongren 554300, Guizhou, China +mixiaoqi1018@163.com + + + +Author + +Wang, Cheng +https://orcid.org/0000-0003-1831-0579 +College of Agriculture and Forestry Engineering and Planning, Guizhou Provincial Key Laboratory of Biodiversity Conservation and Utilization in the Fanjing Mountain Region, Tongren University, Tongren 554300, Guizhou, China + + + +Author + +Gan, Jiahui +https://orcid.org/0000-0001-6899-3705 +College of Agriculture and Forestry Engineering and Planning, Guizhou Provincial Key Laboratory of Biodiversity Conservation and Utilization in the Fanjing Mountain Region, Tongren University, Tongren 554300, Guizhou, China + +text + + +ZooKeys + + +2023 + +2023-08-04 + + +1173 + + +243 +273 + + + + +http://dx.doi.org/10.3897/zookeys.1173.106315 + +journal article +http://dx.doi.org/10.3897/zookeys.1173.106315 +1313-2970-1173-243 +B0A11BACB9DA4DC29BC5F50CE6268CA0 +A6A83DCFCD1D56AABF53E508919088D2 + + + + +Araneus chenjingi +sp. nov. + + + + +Figs 1 +, 2 +, 15A-D +, 17 + + + +Type material. + +Holotype +♂ (TRU- +Araneidae +-178), China: Guizhou Province, Tongren City, Songtao Miao Autonomous County, Wuluo Township, Taohuayuan Village, Yangaoping ( +27°58.71'N +, +108°45.86'E +, ca 1620 m), 2.IV.2022, X.Q. Mi et al. leg. +Paratypes +: 3♀ (TRU- +Araneidae +-179-181), same data as holotype. + + + +Diagnosis. + +The new species resembles + +A. seminiger + +(L. Koch, 1878) in coloration of abdomen, but differs in: 1) conductor membranous, without pointed tip (Fig. +2A-D +) vs heavily sclerotized with a pointed tip ( +Tanikawa 2007 +: fig. 644); 2) embolus visible in prolateral view (Fig. +2A +) vs completely hidden ( +Tanikawa 2007 +: fig. 644); 3) median apophysis about equal width to length in prolateral view (Fig. +2A +) vs ~ 2 +x +longer than wide ( +Tanikawa 2007 +: fig. 644); and 4) scape short, distal end slightly beyond epigastric furrow (Fig. +1A +) vs long, far exceeding epigastric furrow ( +Tanikawa 2007 +: fig. 643). + + + +Description. + +Male +(holotype, Figs +1I, J +, +2 +, +15A-D +). Total length 4.10. Carapace 2.15 long, 1.85 wide. Abdomen 2.85 long, 2.45 wide. Clypeus 0.03 high. Eye sizes and interdistances: AME 0.09, ALE 0.08, PME 0.10, PLE 0.08, AME-AME 0.18, AME-ALE 0.28, PME-PME 0.15, PME-PLE 0.40, MOA length 0.33, anterior width 0.35, posterior width 0.33. Leg measurements: I 7.95 (2.35, 2.85, 2.00, 0.75), II 6.70 (2.00, 2.35, 1.65, 0.70), III 4.35 (1.50, 1.40, 0.95, 0.50), IV 5.90 (1.95, 1.95, 1.45, 0.55). Carapace pear-shaped, yellow to pale green, cervical groove obvious, fovea depressed. Chelicerae yellow, four promarginal teeth and three retromarginal teeth. Endites almost square, with tooth-like process laterally, labium triangular, both yellow to pale green. Sternum cordiform, yellow to pale green, with dark setae. Legs yellow to pale green with dark green annuli, tibia I with 15 macrosetae, tibia II with 13 macrosetae, tibia III with eight macrosetae, tibia IV with 11 macrosetae. Abdomen oval, ~ 1.15 +x +longer than wide, with a pair of very low humps, dorsum pale green with a whitish green spot surrounding by dark markings anteriorly and a triangular dark patch posteriorly; venter grayish brown. Spinnerets yellowish green. + + + +Figure 1. + +Araneus chenjingi + +sp. nov. +A-H +female paratype TRU- +Araneidae +-179 +I, J +male holotype +A +epigyne, ventral view +B +ibid., posterior view +C +ibid., anterior view +D +ibid., lateral view +E +vulva, anterior view +F +habitus, dorsal view +G +ibid., ventral view +H +ibid., lateral view +I +ibid., dorsal view +J +ibid., lateral view. Scale bars: 0.1 mm ( +A-E +); 1 mm ( +F-J +). Abbreviations: CD copulatory duct, CO copulatory opening, FD fertilization duct, Sc scape, Sp spermatheca. + + + + +Figure 2. + +Araneus chenjingi + +sp. nov. male holotype +A +pedipalp, prolateral view +B +ibid., retrolateral view +C +ibid., ventral view +D +ibid., apical view +E +part of expanded bulb. Scale bars: 0.1 mm. Abbreviations: C conductor, E embolus, EL embolic lamella, MA median apophysis, ST subterminal apophysis, TA terminal apophysis. + + + +Pedipalp +(Fig. +2 +): with a basal femoral protrusion; patella with two bristles; median apophysis about equal length to width, with two-pointed tip on opposite sides; embolus slender, almost transversal in prolateral view, curved sharply distally; conductor membranous, widest at base in ventral view; terminal apophysis wide at base, pointed distally, curved into a C-shape in apical view; subterminal apophysis blunt at tip. + + +Female +(paratype TRU- +Araneidae +-179, Fig. +1A-H +). Total length 5.15. Carapace 2.25 long, 1.90 wide. Abdomen 3.45 long, 3.25 wide. Clypeus 0.05 high. Eye sizes and interdistances: AME 0.10, ALE 0.09, PME 0.11, PLE 0.09, AME-AME 0.18, AME-ALE 0.38, PME-PME 0.15, PME-PLE 0.50, MOA length 0.35, anterior width 0.38, posterior width 0.38. Leg measurements: I 7.60 (2.45, 2.70, 1.70, 0.75), II 6.70 (2.15, 2.35, 1.50, 0.70), III 4.00 (1.30, 1.30, 0.85, 0.55), IV 5.95 (1.95, 2.05, 1.35, 0.60). Habitus similar to that of male but the humps on dorsal abdomen a bit higher, and carapace yellow with dark thoracic bilateral sub-margin, endites, labium, sternum, and spinnerets much darker. + + +Epigyne +(Fig. +1A-E +): base of epigyne heavily sclerotized, scape with nearly parallel sides, distal end spoon shaped; copulatory openings arcuated, on the posterior surface; copulatory ducts longer than the spermatheca, twisted into a C-shape; spermathecae oval, about half the spermatheca width apart. + + + +Variation. + +Total length: ♀♀ 4.15-5.20 ( +n += 3). + + + +Distribution. +Known only from type locality. + + +Comments. + +The wide oval female abdomen with a pair of anterior lateral humps, and the long, ridged scape indicate that the new species belongs to the + +A. diadenmatus + +group. + + + +Etymology. +The species is named after Mr. Jing Chen (Fanjingshan National Nature Reserve Administration Bureau), who offered help with specimen collection for this research; noun in genitive case. + + + \ No newline at end of file diff --git a/data/38/B0/91/38B091B6F58272B2B2C6E5577631C845.xml b/data/38/B0/91/38B091B6F58272B2B2C6E5577631C845.xml new file mode 100644 index 00000000000..b1615da3796 --- /dev/null +++ b/data/38/B0/91/38B091B6F58272B2B2C6E5577631C845.xml @@ -0,0 +1,67 @@ + + + +The ground beetles (Coleoptera: Carabidae) of the Strandzha Mountain and adjacent coastal territories (Bulgaria and Turkey) + + + +Author + +Kostova, Rumyana + + + +Author + +Gueorguiev, Borislav + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8135 +8135 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8135 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8135 +1314-2828-4-8135 + + + + +Microlestes fissuralis (Reitter, 1901) + + + +Materials + + +Type status: +Other material +. Location: countryCode: BG; locality: +Ahtopol +; Record Level: bibliographicCitation: Hieke & Wrase (1988: 159) + + +Type status: +Other material +. Location: countryCode: BG; locality: +Tsarevo (= Micurin) +; Record Level: bibliographicCitation: Hieke & Wrase (1988: 159) + + + + + \ No newline at end of file diff --git a/data/38/B1/48/38B14821E0C45BEBB46C83C26C619DA0.xml b/data/38/B1/48/38B14821E0C45BEBB46C83C26C619DA0.xml new file mode 100644 index 00000000000..3077d15a19a --- /dev/null +++ b/data/38/B1/48/38B14821E0C45BEBB46C83C26C619DA0.xml @@ -0,0 +1,394 @@ + + + +The bee genus Anthidiellum in Vietnam: descriptions of five new species and the first male of Anthidiellum coronum (Hymenoptera, Megachilidae) + + + +Author + +Tran, Ngat Thi +Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Road, Nghia Do, Cau Giay, Hanoi, Vietnam & Graduate University of Science and Technology, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Road, Nghia Do, Cau Giay, Hanoi, Vietnam +tranthingat1012@gmail.com + + + +Author + +Engel, Michael S. +https://orcid.org/0000-0003-3067-077X +Division of Invertebrate Zoology, American Museum of Natural History, Central Park West at 79 & th +msengel@ku.edu + + + +Author + +Nguyen, Cuong Quang +Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Road, Nghia Do, Cau Giay, Hanoi, Vietnam + + + +Author + +Tran, Duong Dinh +Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Road, Nghia Do, Cau Giay, Hanoi, Vietnam + + + +Author + +Nguyen, Lien Thi Phuong +Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Road, Nghia Do, Cau Giay, Hanoi, Vietnam & Graduate University of Science and Technology, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Road, Nghia Do, Cau Giay, Hanoi, Vietnam + +text + + +ZooKeys + + +2023 + +2023-02-02 + + +1144 + + +171 +196 + + + + +http://dx.doi.org/10.3897/zookeys.1144.98644 + +journal article +http://dx.doi.org/10.3897/zookeys.1144.98644 +1313-2970-1144-171 +C11074779CE243F9998521D42836A8F4 +D148129EDAED5CD0ACA97302FBE35254 + + + + +Anthidiellum (Pycnanthidium) carinatum (Wu, 1962) + + + + +Figs 3A-G +, 4A-F + + + + +Paraanthidium carinatum +Wu, 1962: 165 [holotype ♂, paratype ♀]. Wu et al. 1988: 61. + + +Trachusa (Paraanthidium) carinatum +(Wu): Wu 2006: 181. + + +Anthidiellum (Pycnanthidium) carinatum +(Wu): +Niu et al. 2016 +: 337. + + + +Material examined. + + +Vietnam +: +2♀♀ +, +Son La +, +Moc Chau +, +Nam Kham +, alt. + +630 m + +, +22.vi.2020 +[ +22 June 2020 +], +Lien Thi Phuong Nguyen +, +Cuong Quang Nguyen +, +Ngat Thi Tran +, +Thai Van Mai +leg. + +[ +1♀ +in IEBR, +1♀ +in AMNH]; + +1♀ +; +Son La +, +Moc Chau +, +27.vi.2022 +, +Lien Thi Phuong Nguyen +, +Lam Xuan Truong +, +Cuong Quang Nguyen +, +Ngat Thi Tran +leg. + +,; + +1♀ +, +Vinh Phuc +, +Me Linh station +, +12.vi.2018 +[ +12 June 2018 +], +Phong Huy Pham +leg. + +; + +3♂♂ +, +Kon Tum +, +Sa Thay +, +Chu Mom Ray +NP, +14°47'24.5"N +, +107°59'46.5"E +, alt. + +729 m + +, +25.iv.2016 +[ +25 April 2016 +], +Lien Thi Phuong Nguyen +, +Dai Dac Nguyen +, +Ngat Thi Tran +leg. + +[IEBR]; + +6♂♂ +, +Kon Tum +, +Sa Thay +, +Chu Mom Ray +NP, +Ro Koi +RS, +14°27'25"N +, +107°36'22"E +, alt. + +267 m + +, +25.iv.2022 +[ +25 June 2022 +], +Lien Thi Phuong Nguyen +, +Ngat Thi Tran +leg. + +[ +4♂♂ +in IEBR, +2♂♂ +in AMNH]; + +3♀♀ +, +Gia Lai +, +Mang Yang +, +Ayun +, +Kon Ka Kinh +NP, +14°13'18"N +, +108°19'02"E +, alt. + +907 m + +, +26.iii.2022 +[ +26 March 2022 +], +Lien Thi Phuong Nguyen +, +Ngat Thi Tran +, +Cuong Quang Nguyen +leg. + +; + +1♀ +, +Gia Lai +, +Mang Yang +, +Ayun +, +Kon Ka Kinh +NP, +14°12'11"N +, +108°18'58"E +, alt. + +834 m + +, +25.iii.2022 +[ +25 March 2022 +], +Lien Thi Phuong Nguyen +, +Ngat Thi Tran +, +Cuong Quang Nguyen +leg. + +; + +1♂ +, +Dak Lak +, +Krong Bong +, +Krong Kmar +, +Chu Yang Sin +NP, +12°28'46.4"N +, +108°13'46.4"E +, alt. + +739 m + +, +2.v.2016 +[ +2 May 2016 +], +Lien Thi Phuong Nguyen +, +Dai Dac Nguyen +, +Ngat Thi Tran +leg. + +[IEBR]. + + + +Remarks. + +This species can be separated from the similar species + +A. smithii + +(Ritsema) by the following combination of traits: punctures of mesoscutum mesad parapsidal line dense but not contiguous; axilla laterally not reaching tangent of lateral margin of mesoscutum; and clypeus more densely, finely punctate, and posterior margin of gena not as strongly carinate posteriorly. + + + +Nesting biology. + +A nest was found in an unused wooden plank in a warehouse in Son La Province. The entrance hole of the nest was oval-shaped, with a length and a width of about 4 mm and 3 mm, respectively (Fig. +3G +). A female was observed and collected when flying out from the nest. + + + +Figure 3. +Anthidiellum (Pycnanthidium) carinatum +(Wu, 1962), female +A +lateral habitus +B +dorsal-posterior habitus +C +facial view +D +mesosoma in dorsal view +E +mesosoma in lateral view, red arrow indicating omaular carina +F +prolateral surfaces of metatibia and metatarsus, with red arrows indicating longitudinal carinae +G +nest entrance. Scale bars: 1 mm ( +A, B, E +); 0.5 mm ( +C, D, F +). + + + + +Figure 4. +Anthidiellum (Pycnanthidium) carinatum +(Wu, 1962), male +A +lateral habitus +B +dorsal-posterior habitus +C +facial view +D +mandibles +E +mesosoma in lateral view, red arrow indicating omaular carina +F +apical metasomal sterna, red arrow indicating apical comb. Scale bars: 1 mm ( +A, B +); 0.5 mm ( +C-F +). + + + + + \ No newline at end of file diff --git a/data/38/B1/DF/38B1DF66518F94FA6EA501A59609E0D0.xml b/data/38/B1/DF/38B1DF66518F94FA6EA501A59609E0D0.xml new file mode 100644 index 00000000000..6b807845a80 --- /dev/null +++ b/data/38/B1/DF/38B1DF66518F94FA6EA501A59609E0D0.xml @@ -0,0 +1,105 @@ + + + +The " Martian " flora: new collections of vascular plants, lichens, fungi, algae, and cyanobacteria from the Mars Desert Research Station, Utah + + + +Author + +Sokoloff, Paul C. + + + +Author + +Freebury, Colin E. + + + +Author + +Hamilton, Paul B. + + + +Author + +Saarela, Jeffery M. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8176 +8176 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8176 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8176 +1314-2828-4-8176 + + + + +Hymenoxys cooperi (A. Gray) Cockerell + + + +Materials + + +Type status: +Other material +. Occurrence: recordNumber: 312; recordedBy: +Sokoloff, Paul C. +; preparations: Silica gel collection; Taxon: scientificName: Hymenoxyscooperi (A. Gray) Cockerell; kingdom: Plantae; phylum: Angiosperms; class: Eudicots; order: Asterales; family: Asteraceae; genus: Hymenoxys; specificEpithet: cooperi; taxonRank: Species; scientificNameAuthorship: (A. Gray) Cockerell; Location: continent: North America; country: +United States of America +; countryCode: USA; stateProvince: Utah; county: Wayne County; municipality: Hanksville; locality: +Mars Desert Research Station +; verbatimLocality: Sandstone plateau immediately southwest of Mars Desert Research Station, alongside ATV trail; verbatimElevation: +1412 m +; verbatimLatitude: +38°24'22.4"N +; verbatimLongitude: +110°47'40.3"W +; coordinateUncertaintyInMeters: 50; Identification: identifiedBy: +Sokoloff, Paul C. +; dateIdentified: 2015; Event: verbatimEventDate: +November 24, 2014 +; habitat: Dry conglomerate sandstone; Record Level: institutionID: CMN; collectionID: CAN 607483; collectionCode: +CAN +; basisOfRecord: Preserved Specimen + + + + +Notes + +This species, collected on the plateau west of MDRS, was not recorded in the previous floristic survey of the nearby San Rafael Swell +Harris (1983) +but there is a record of this species occurring in the Glen Canyon Recreational Area to the south ( +Hill and Ayers 2009 +). A shorter form with fewer heads is sometimes recognized as +H. cooperi var. canescens +(D.C. Eaton) K. F. Parker; however +Welsh et al. (1993) +did not recognize varieties in Utah, and +Bierner (2006) +did not recognize varieties in this species whatsoever. + +Supplemental File: CAN 607483 (Suppl. material 37). + + + \ No newline at end of file diff --git a/data/38/B2/B8/38B2B829A720EBDE91DD42096CE88DE2.xml b/data/38/B2/B8/38B2B829A720EBDE91DD42096CE88DE2.xml new file mode 100644 index 00000000000..b2fbaf171ee --- /dev/null +++ b/data/38/B2/B8/38B2B829A720EBDE91DD42096CE88DE2.xml @@ -0,0 +1,173 @@ + + + +Order Cetacea + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +723 +743 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Neophocaena phocaenoides +(G. Cuvier 1829) + + + + + + + +[Delphinus] phocaenoides +G. Cuvier 1829 + +, +Regn. Anim., Nouv. ed., Vol. 1: 291 + +. + + + + +Type Locality: + +South Africa +, +Western Cape Prov. +, +Cape +of Good Hope ("à découvert au Cap,"). Almost certainly erroneous; unknown today from coast of Africa. + + + + + +Vernacular Names: +Finless Porpoise +. + + + + +Subspecies: +: + + +Subspecies + +Neophocaena phocaenoides +subsp. +phocaenoides +G. Cuvier 1829 + + + +Subspecies + +Neophocaena phocaenoides +subsp. +asiaeorientalis +Pilleri and Gihr 1972 + + + +Subspecies + +Neophocaena phocaenoides +subsp. +sunameri +Pilleri and Gihr 1975 + + + + + +Distribution: +Indo-Pacific: warm-temperate to tropical waters; Persian Gulf to +Malaysia +, north coast of Java (Tasàn and Leatherwood, 1984), +China +, and +Japan +: coastal waters and some rivers. + + + + +Conservation: +CITES +– Appendix I; +IUCN +– Endangered as +N. p. asiaeorientalis +, otherwise Data Deficient. + + + + +Discussion: +Reviewed by +Pilleri and Gihr (1972 +; +1975:657 +, 673; 1980 +b +). +Van Bree (1973) +considered +asiaeorientalis +to be of subspecific rank and +sunameri +to be synonymous with + +phocaenoides + +. +Rice (1998:123) +recognized + +N. p. +phocaenoides + +, +N. p. sunameri +(Sunameri) and +N. p. asiaeorientalis +(Yangtse River Porpoise). + + + + \ No newline at end of file diff --git a/data/38/B2/D0/38B2D0FB596BAA0CF0B073C563084F49.xml b/data/38/B2/D0/38B2D0FB596BAA0CF0B073C563084F49.xml new file mode 100644 index 00000000000..88056403d8e --- /dev/null +++ b/data/38/B2/D0/38B2D0FB596BAA0CF0B073C563084F49.xml @@ -0,0 +1,117 @@ + + + +Order Soricomorpha + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +220 +311 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Crocidura theresae +Heim de Balsac 1968 + + + + + + + +Crocidura theresae +Heim de Balsac 1968 + +, + +Mammalia +, 32: 398 + + +. + + + + +Type Locality: + +Guinea +, Nzerekore. + + + + + +Vernacular Names: +Therese's Shrew +. + + + + +Distribution: +Guinea +savanna from +Ghana +to +Guinea +. + + + + +Conservation: +IUCN +– Lower Risk (lc). + + + + +Discussion: +May be a subspecies of + +foxi + +, but + +theresae + +from +Côte +d’Ivoire are distinctly smaller and grayer. Karyotype has 2n = 50, FN = 82-84 (Meylan, 1971). + + + + \ No newline at end of file diff --git a/data/38/B3/40/38B3409DDD5D54BF8B406D26A0358542.xml b/data/38/B3/40/38B3409DDD5D54BF8B406D26A0358542.xml new file mode 100644 index 00000000000..5d98194474c --- /dev/null +++ b/data/38/B3/40/38B3409DDD5D54BF8B406D26A0358542.xml @@ -0,0 +1,285 @@ + + + +Novel taxa and species diversity of Cordyceps sensu lato (Hypocreales, Ascomycota) developing on wireworms (Elateroidea and Tenebrionoidea, Coleoptera) + + + +Author + +Zha, Ling-Sheng +https://orcid.org/0000-0003-4935-0725 +School of Life Sciences, Huaibei Normal University, Huaibei 235000, P. R. China & School of Sciences, Mae Fah Luang University, Chiang Rai 57100, Thailand & Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand + + + +Author + +Kryukov, Vadim Yu +Institute of Systematics and Ecology of Animals, Siberian Branch of Russian Academy of Sciences, Frunze str., 11, Novosibirsk 630091, Russia + + + +Author + +Ding, Jian-Hua +https://orcid.org/0000-0002-0348-9847 +School of Life Sciences, Huaibei Normal University, Huaibei 235000, P. R. China + + + +Author + +Jeewon, Rajesh +https://orcid.org/0000-0002-8563-957X +Department of Health Sciences, Faculty of Medicine and Health Sciences, University of Mauritius, Reduit 80837, Mauritius + + + +Author + +Chomnunti, Putarak +School of Sciences, Mae Fah Luang University, Chiang Rai 57100, Thailand & Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand +putarak.cho@mfu.ac.th + +text + + +MycoKeys + + +2021 + +2021-03-29 + + +78 + + +79 +117 + + + + +http://dx.doi.org/10.3897/mycokeys.78.61836 + +journal article +http://dx.doi.org/10.3897/mycokeys.78.61836 +1314-4049-78-79 +A7805105FFAF5D3EA781AE792370B9B9 + + + + +Ophiocordyceps borealis L.S. Zha & P. Chomnunti +sp. nov. +Fig. 2 + + + +Etymology. +Referring to the region (south of boreal zone of the Russian Far East) from where the species was collected. + + +Sexual morph. + +Parasitising +Elateroidea +larvae ( +Coleoptera +) living in fallen wood. The larvae are cylindrical, 11 mm long and 1.1-1.3 mm thick, yellowish-brown; their body cavity stuffed with milky yellow mycelia and their intersegmental membranes covered with many milky yellow and flocculent funiculi. +Stromata +arising from any part of larval body, single or paired, unbranched. Stipe grey, slender and cylindrical, fibrous and flexible, curved more or less, 10-13 mm long and 0.25-0.6 mm thick, surface relatively smooth but with many longitudinal wrinkles, apex pointed. +Fertile part +irregularly attached on one side of the surface of distal part of stipe, which resembles a mass of insect eggs that are clustered together or separated into several lumps; substrate layer milky white, surface milky yellow accompanied by lavender and dotted with numerous black ostioles. +Perithecia +immersed, densely arranged, obliquely or at right angles to the surface of stipe, pyriform, neck unconspicuous, 220-290 +x +120-150 +µm +and their tops obtuse; walls dark brown and 25-32 +µm +thick; ostioles slightly thickened and slightly protruding over the surface of fertile part. +Asci +cylindrical, 6-8 +µm +in diameter; caps hemispherical, 5-6 ( +x +- = 5.5, n = 30) +µm +wide and 3.5-5 ( +x +- = 4.2, n = 30) +µm +high. +Ascospores +filiform and elongate, multi-septate (far more than 3), not easy to break into part-spores; part-spores cylindrical, truncated at both ends, 10-15 ( +x +- = 12.2, n = 30) +x +2 +μm +. +Asexual morph. +Unknown. + + + +Figure 2. + +Ophiocordyceps borealis + +a-c +stromata arising from the different parts of larval bodies +d +apical ends of stromata +e +transverse section of fertile part, on which densely arranged perithecia are shown +f +asci +g +ascospores. Scale bars: 2 mm ( +a-c +); 1 mm ( +d +); 100 +µm +( +e +), 10 +µm +( +f, g +). + + + + +Material examined. + + +Russia +, the +Russian Far East +, +Primorskiy Krai +, +National Park Land +of the +Leopard +, + +Natural Reserve +Kedrovaya Pad + +, +43°05'53.8"N +, +131°33'17.8"E +, +10 August 2016 +, +Oksana Tomilova +& +Vadim Yu Kryukov +(MFLU 18-0163, + +holotype + +; GACP +R16002 +and GACP +R16003 +, + +paratypes + +) + +. + + + +Known distribution. +Russia (Primorskiy Krai). + + +Hosts. + +Growing on +Elateroidea +larvae ( +Coleoptera +) living in fallen wood in a deciduous forest. + + + +Notes. + +The new species is morphologically similar to + +O. purpureostromata + +(≡ + +C. purpureostromata + +), but their stipes and ascospores are distinct. In + +O. purpureostromata + +, stipe is thicker (0.6-1 mm in diameter) and has hairs (0.25-0.6 mm in diameter and without hair in + +O. borealis + +), ascospores are only 65-75 +x +10 +µm +long and 3-septate (elongate and far more than 3-septate in + +O. borealis + +) and part-spores are 13-23 +µm +long (10-15 +µm +long in + +O. borealis + +) ( +Kobayasi and Shimizu 1980b +). + + +Nucleotide sequences of + +O. borealis + +are most similar to those of + +O. purpureostromata + +(specimen TNS F18430, +Quandt et al. 2014 +), but there is 2.3% bp difference across the 804 bp in TEF1-α, 0.5% bp difference across the 845 bp in LSU and 0.1% bp difference across 1,061 bp in SSU. ITS of + +O. borealis + +is> 14.1% different to all ITS available in GenBank (ITS are not available for + +O. purpureostromata + +). On the phylogenetic tree, the new species is also nearest (100% ML/100% MP/1.00 PP) to + +O. purpureostromata + +, but they form into two distinct branches which support them being two separate species (Fig. +1 +). + + + + \ No newline at end of file diff --git a/data/38/B3/A5/38B3A5E8D15C22B630490312A890AF13.xml b/data/38/B3/A5/38B3A5E8D15C22B630490312A890AF13.xml new file mode 100644 index 00000000000..5553da4359c --- /dev/null +++ b/data/38/B3/A5/38B3A5E8D15C22B630490312A890AF13.xml @@ -0,0 +1,245 @@ + + + +Differential patterns of ophiostomatoid fungal communities associated with three sympatric Tomicus species infesting pines in south-western China, with a description of four new species + + + +Author + +Min Wang, Hui + + + +Author + +Wang, Zheng + + + +Author + +Liu, Fu + + + +Author + +Xu Wu, Cheng + + + +Author + +Fang Zhang, Su + + + +Author + +Kong, Xiang Bo + + + +Author + +Decock, Cony + + + +Author + +Lu, Quan + + + +Author + +Zhang, Zhen + +text + + +MycoKeys + + +2019 + +50 + + +93 +133 + + + + +http://dx.doi.org/10.3897/mycokeys.50.32653 + +journal article +http://dx.doi.org/10.3897/mycokeys.50.32653 +1314-4049-50-93 + + + + +Leptographium yunnanense X.D. Zhou, K. Jacobs, M.J. Wingf. & M. Morelet, Mycoscience 41(6): 576. 2000. +Fig. 12 + + + +Description. +Sexual form: unknown. + +Asexual form: +Leptographium +-like. Conidiophores occurring singly or in groups of up to three, arising from the superficial mycelium, erect, macronematous, mononematous, (93.5-) 159-412 (-544) +μm +long, without rhizoid-like structures; stipes simple, cylindrical, not constricted at septa, 1-6-septate, pale olivaceous at the base, (12-) 19.0-128 (-245) +x +(3.3-) 4.1-6.1 (-7.3) +μm +; conidiogenous apparatus (33.0-) 65.5-119.5 (-168.0) +μm +long (high), with 2 to 3 series of cylindrical branches; primary branches hyaline to pale olivaceous, smooth, cylindrical, 2-3 septate, (11.5-) 18.2-37.7 (-56.0) +μm +long and (3.0-) 3.7-5.9 (-7.7) +μm +wide; secondary branches hyaline, 0-2 septate, (10.3-) 14.5-30.0 (-50.1) +μm +long, (2.8-) 3.4-5.5 (-7.3) +μm +wide; conidiogenous cells discrete, 2-3 per branch, cylindrical, (10.2-) 13.2-29.6 (-57.4) +x +(2.2-) 2.9-3.9 (-4.4) +μm +; conidia 1-celled, oblong to obovoid with truncate bases, hyaline, (5.8-) 7.0-10.4 (-13.0) +x +(2.9-) 3.6-5.3 (-6.4) +μm +. + + + +Figure 12. Morphological characters of +Leptographium yunnanense +A, B upper and reverse of cultures on 2% MEA 8 d after inoculation D, I conidiophore on 2% MEA C, +E-H +conidiogenous cells of +Leptographium +-like asexual state and conidia. Scale bars: 50 +μm +(D, I); 10 +μm +(C, +E-H +). + + + + +Culture characteristics. +Colonies on 2% MEA medium fast growing in the dark, reaching 76 mm in diam. in 8 days at 25 °C, growth rate up to 20 mm/day at the fastest; colony margin smooth. Hyphae submerged in agar with aerial mycelium, greenish-olivaceous to olivaceous, smooth, straight; reverse hyphae umber-brown to dark olivaceous. Optimal growth temperature 25 °C, slow growth at 5 °C and 30 °C. + + +Known substrate and hosts. + +Tomicus yunnanensis +and its galleries in +Pinus yunnanensis +, galleries of +T. brevipilosus +in +P. kesiya +. + + + +Known insect vectors. + +Tomicus brevipilosus +, +T. yunnanensis +. + + + +Known distribution. +Yunnan Province, China. + + +Specimens examined. + +CHINA, Yunnan, adults of +Tomicus yunnanensis +and their galleries in +Pinus yunnanensis +, +Tomicus brevipilosus +galleries in +P. kesiya +. Apr. 2017, HM Wang, CFCC 52619 = CXY 1897, CFCC 52620 = CXY 1900, CFCC 52621 = CXY 1904, CFCC 52622 = CXY 1908, CFCC 52623 = CXY 1917, CFCC 52624 = CXY 1925. + + + + +Note +. + + +The sole reproductive structure formed on MEA in +L. yunnanense +is a +Leptographium +-like state. Our strains were identified as +L. yunnanense +, based on phylogenetic evidence and secondarily, on morphological features. However, our strains slightly deviated from +L. yunnanense +in having longer conidiophores, mainly 159-412 +μm +vs mostly 74-227 (-233) +μm +( +Zhou et al. 2000 +) or 80-240 +μm +( +Yamaoka et al. 2008 +). Furthermore, our strains grew faster than reported for the species, 76 mm vs 44 mm in 8 days at 25 °C ( +Zhou et al. 2000 +). + + +Although our strains were slightly genetically and morphologically divergent, we are of the opinion that they enter into the current +L. yunnanense +species concept (e.g. sensu +Zhou et al. 2000 +). +Yamaoka et al. (2008) +showed the genetic diversity of +L. yunnanense +in Yunnan to be higher than in other places, that which is confirmed by the present study. + + +Leptographium yunnanense +was originally described from Yunnan Province with only an asexual state ( +Zhou et al. 2000 +). Subsequently, mating of strains from different origins (Thailand, China and Japan) yielded the sexual state, which is formed by neckless ascocarps and cucullate ascospores ( +Yamaoka et al. 2008 +). + + +Leptographium yunnanense +was the third most abundant species associated with +T. yunnanensis +in our study. A few strains also were isolated from +T. brevipilosus +infesting +P. kesiya +and none from +T. minor +. + + + + \ No newline at end of file diff --git a/data/38/B4/45/38B445ACF95974055D22C70E291DF1DC.xml b/data/38/B4/45/38B445ACF95974055D22C70E291DF1DC.xml new file mode 100644 index 00000000000..a4ad501164f --- /dev/null +++ b/data/38/B4/45/38B445ACF95974055D22C70E291DF1DC.xml @@ -0,0 +1,100 @@ + + + +10. Rosa L. + + + +Author + +I. Klášterský + +text + + +1968 +Cambridge University Press + +Cambrdige + + + + +Editor + +T. G. Tutin + + + +Editor + +V. H. Heywood + + + +Editor + +N. A. Burgess + + + +Editor + +D. M. Moore + + + +Editor + +D. H. Valentine + + + +Editor + +S. M. Valters + + + +Editor + +D. A. Webb + + +Flora Europaea, Volume 2, Rosaceae to Umbelliferae + + + +35 +42 + + + +book chapter +10.5281/zenodo.47067 + + + + +28. +R. obtusifolia +Desv., + + + + +Jour. Bot. Redige 2: 317 (1809) ( + +R. tomentella +Leman + +, +R. klukii +Besser). + + + +Stems up to 2 m, green; prickles scattered, short, stout, compressed, strongly hooked. Leaflets 5-7, 15-35 x 14-25 mm, broadly ovate, simply to compound-serrate, softly appressed-pubescent on both surfaces, sometimes pubescent only on the veins beneath, usually glandular on the veins beneath; teeth glandular, short and wide; petiole and rhachis densely pubescent, more or less glandular, covered with minute acicles. Pedicels 5-15 mm, glabrous. Sepals eglandular, deflexed and caducous after anthesis. Petals 12-18(-24) mm, white or pale pink. Disc wide, with the orifice less than 1 mm wide. Styles long-exserted, villous or rarely glabrous. Fruit 10-20 mm, ovoid or globose, glabrous, red. C., S. & N.W. Europe. A1 Au Be Br Bu Co Cz Da Ge Gr Hb He Hu It Ju Po Rm Rs (W, C) Sa Si Su. + + + \ No newline at end of file diff --git a/data/38/B4/4F/38B44F11210A030B77F1DEA13F2DEA95.xml b/data/38/B4/4F/38B44F11210A030B77F1DEA13F2DEA95.xml new file mode 100644 index 00000000000..c72f1f5ebf9 --- /dev/null +++ b/data/38/B4/4F/38B44F11210A030B77F1DEA13F2DEA95.xml @@ -0,0 +1,88 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part C) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +370 +473 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Chenopodium vulvaria +Linnaeus + +, + +Species Plantarum +1 + +: 220. 1753 + + +. + + + +"Habitat in Europae cultis oleraceis." RCN: 1811. + + + + +Lectotype +(Jafri & Rateeb in Jafri & El-Gadi, +Fl. Libya +58: 15. 1978): Herb. Linn. No. 313.18 ( +LINN +) + +. + + + + +Current name: + + +Chenopodium vulvaria + +L. + +( +Chenopodiaceae +). + + + + \ No newline at end of file diff --git a/data/38/B4/5D/38B45D86E65A2431D177BDEEC5EE769F.xml b/data/38/B4/5D/38B45D86E65A2431D177BDEEC5EE769F.xml new file mode 100644 index 00000000000..9dcaeb7f04f --- /dev/null +++ b/data/38/B4/5D/38B45D86E65A2431D177BDEEC5EE769F.xml @@ -0,0 +1,84 @@ + + + +Hornmilben (Oribatida) [pages 69 to 101] + + + +Author + +Weigmann, G. + + + +Author + +Miko, L. + +text + + +2006 +Goecke & Evers + +Keltern + + + +Hornmilben (Oribatida) [Dahl, Tierwelt Deutschlands, Teil 76] + + + +69 +101 + + + + +http://www.goeckeevers.de/verlag/dahl.html + +book chapter +Weigmann2006pp69to101 + + + + +Sellnickochthonius hungaricus +(Balogh, 1943) [46b] + + + + +Syn., Tax.: +Poecilochthonius hungaricus +Balogh, 1943. +Brachychochthonius h. +: Strenzke 1951b (B); Sellnick 1960; Moritz 1976b (B); Balogh & Mahunka 1983 (B). +Brachychthonius h. +: Evans 1952b (B). + + + + +- " +Brachychochthonius rostratus +": Niedbala 1974 (B). + + + + +Oekologie +: Schwerpunkt in verschiedenen +Waldboeden +. + + + + +Verbreitung: +Palaearktis +. + + + + \ No newline at end of file diff --git a/data/38/B4/79/38B479FFA52A588DAC8705AC08771DC8.xml b/data/38/B4/79/38B479FFA52A588DAC8705AC08771DC8.xml new file mode 100644 index 00000000000..1a22eae5ff0 --- /dev/null +++ b/data/38/B4/79/38B479FFA52A588DAC8705AC08771DC8.xml @@ -0,0 +1,362 @@ + + + +Revision of the Palearctic species of Fidiobia Ashmead (Hymenoptera, Platygastroidea) + + + +Author + +Popovici, Ovidiu Alin +https://orcid.org/0000-0001-5926-2177 +' Al. I. Cuza' University of Iasi, Faculty of Biology, Research Group in Invertebrate Diversity and Phylogenetics, CERNESIM, B-dul Carol I, no. 11, Iasi, Romania +popovici_alin_ovidiu@yahoo.com + + + +Author + +Masner, Lubomir +Agriculture and Agri-Food Canada, K. W. Neatby Building, Ottawa, Ontario K 1 A 0 C 6, Canada + + + +Author + +Lahey, Zachary +https://orcid.org/0000-0002-9402-9570 +United States Department of Agriculture, Agricultural Research Service, U. S. Vegetable Laboratory, Charleston, SC, USA + + + +Author + +Talamas, Elijah +https://orcid.org/0000-0002-1048-6345 +Florida State Collection of Arthropods, Division of Plant Industry, Florida Department of Agriculture and Consumer Services, Gainesville, FL, USA + +text + + +Journal of Hymenoptera Research + + +2022 + +2022-08-31 + + +92 + + +23 +144 + + + + +http://dx.doi.org/10.3897/jhr.92.85040 + +journal article +http://dx.doi.org/10.3897/jhr.92.85040 +1314-2607-92-23 +4B9051158FA1412F9D06FAA908449CAF +CAD7522EF5EF5E23AE107BBD3BA4C21B + + + + +4. +Fidiobia communis Popovici, Masner & Talamas +sp. nov. + + + + +Figs 56-60 +, 301 + + + +Description. + +Female. +Body length: 0.8-0.9 mm. Colour of body: melanic (Figs +56a +, +58 +). + + +Head +(Fig. +56a +). Colour of head: brown. Sculpture of head: reticulate-coriaceous. Sculpture of occiput: transverse reticulate coriaceous. Ocellar prominence: absent. Preocellar depression: present. Paraocellar depressions: present. OOL / ocellar diameter: OOL equal with ocellar diameter. Orientation of lower half of inner orbits: visibly divergent. Sculpture of frons immediately anterior to ocellus: reticulate-coriaceous. Sculpture of frons immediately dorsal to toruli: the same with the sculpture from the rest of frons, but more transverse. Epitorular carina: present. Distance between toruli: equal to the transverse diameter of torulus. Setation of clypeus: two setae. Malar sulcus: absent. +Antenna +(Fig. +56b +). Colour of A1: light brown. Colour of clava: slightly darker than the rest of antenna. Number of antennomeres: nine. Shape of A1: more or less cylindrical. Ventral (inner) lamella on A1: present as a trace in the apical part of A1. Length of A3 of female: distinctly shorter than A2. Sensillar formula (A7:A8:A9): 2:2:1. + + + +Figures 56-60. + +Fidiobia communis + +: +56a +female, habitus, dorsal view (Holotype) +56b +antenna (♀) +57a +male, habitus, dorsal view (OPPC0578) +57b +antenna (♂) +58 +female, habitus, lateral view +59 +female, mesosoma, lateral view +60a +wings +60b +WIP. + + + +Mesosoma +(Figs +56a +, +59 +). Colour of mesosoma: brown. Mesosoma: weakly compressed dorsoventrally. Pronotum in dorsal view: narrow, collarlike. Transverse pronotal sulcus: present as a narrow groove along anterior rim of pronotum. Posteroventral end of transverse pronotal sulcus: dilated. Lateral pronotal area: sculptured only on the dorsal half. Antero-admedian line: absent. Mesoscutum: weakly convex. Parapsidal lines: absent. Sculpture of internotaular area: absent. Notauli: present, incised. Shape of notauli: dilated posteriorly and acute anteriorly. Outer edge of notauli: almost collinear with axillular carina. Orientation of inner edge of notauli: converging posteriorly. Length of notauli: at most 0.3 times as long as mesoscutellum, measured along midline. Length of notaulus / maximum width of notaulus: 2.0-2.9 times as long as wide. Distance between notauli: greater than the broadest part of notaulus. Transscutal articulation: complete. Scuto-scutellar sulcus: absent. Fovea on scuto-scutellar sulcus: NA. Mesoscutellum: weakly convex. Shape of mesoscutellum: subrectangular. Axillular carina: posterior apex of axillular carinae touching the posterior edge of mesoscutellum. Axilloaxillular carina: present. Sculpture of mesoscutellum: absent. Posterior mesoscutellar sulcus: absent. Metascutellum: entirely visible. Metascutellar carina: present. Width of metasomal depression: greater than the length of lateral propodeal carina. Median carina between lateral propodeal carinae: absent. Transverse carina between lateral propodeal carinae: present. Foamy structure on transverse carina between lateral propodeal carinae: present. Foamy structure on metasomal depression: absent. Lateral propodeal carinae: parallel. Foamy structure on lateral propodeal carina: present only on the posterior half of the vertical part. Plica: visible. Posterior end of plica: free, converging with metapleural carina. Foamy structure on plica: present, fused with foamy structure from metapleural carinae. Foamy structure on metapleural carina: present on the entire carina. Foamy structure on ventral metapleural area: present. Setation of dorsal metapleural area: sparse, long setae in 2-3 longitudinal rows. Setation of ventral metapleural area: dense, long setae on posteroventral half. Longitudinal striation on dorsal mesopleuron: present. Transepisternal line: absent. Mesopleural carina: present. Metapleural sulcus: present, from incomplete to complete. +Wings +(Figs +60a,b +): macropterous. Apex of fore wing: rounded. Colour of fore wing: infuscate. Transverse brown band on fore wing: absent. Submarginal vein in fore wing: present. Length of submarginal vein in fore wing: not surpassing basal 1/4 the length of fore wing. Spectral veins on fore wing: absent. Marginal setae of fore wing: present, well visible. Disc of fore wing: with spinulose microtrichia. +Legs +. Colour of fore tibia: light brown. Colour of fore tarsus: light brown. Colour of middle femora: light brown. Colour of middle tibiae: light brown. Colour of middle tarsus: light brown. Colour of hind femora: light brown. Colour of hind tibiae: light brown. Colour of hind tarsus: light brown. + + + +Metasoma +. + +Posterior of T2 some or all tergites may be retracted under T2. Shape of T1: trapezoidal. Colour of T1: brown. Lateral setae of T1: 2 pairs. Colour of T2: brown. Shape of T2: longer than wide. Anterior pits of T2: distinctly separated. Sculpture of T2, lateral to anterior pits of T2: absent. Colour of T3-T5: the same as T2. + + +Male +(Fig. +57a +): similar to the female, differing in the structure of the antenna (Fig. +57b +). + + + +Etymology. + +This species is named " +communis +" because of the absence of any peculiar or striking characters. + + + +Material examined. + + +6♀ +and +1♂ +. +Romania +: + +Holotype + +1♀ +, +Suceava +, +Călimani +Mts., road of +Maria Teresa +, +47.12346°N +, +25.20249°E +, +13-20.vii.2012 +, leg. +Popovici O. +(SS) (OPPC0577). + + + + + +Paratypes + +: +Czech Republic +: +1♀ + +, + +Bohemia +, +Celakovice +Lipovka Res., +50.177°N +, +14.759°E +, +2-19.vi.1994 +, leg. +Macek J. +(MT) (CNCI) + +. + + + +Estonia +: +2♀ +, +1.5 km +NE + +Soeoeru + +, +58.66111°N +, +26.88531°E +, +4-11.vii.2011 +, leg. +Soon V. +(SN) (OPPC0664, 0665) + +. + + + +Romania +: +1♂ +, +Suceava +, +Călimani +Mts., road of +Maria Teresa +, +47.12346°N +, +25.20249°E +, +13-20.vii.2012 +, leg. +Popovici O. +(SS) (OPPC0578) + +. + + + +Ukraine +: +1♀ +, +Transcarpathia +, +Svydovets +, + +2-3 km +NW of Kvasy + +, +48.15247°N +, +24.26621°E +, +7.v-5.vi.2014 +, leg. +Varga O. +(TT) (OPPC0230) + +; + +1♀ +, +Transcarpathia +, +Svydovets +, + +2-3 km +NW of Kvasy + +, +48.15247°N +, +24.26621°E +, +5-29.vi.2014 +, leg. +Varga O. +(TT) (OPPC0146) + +. + + + +Distribution. + +Czech Republic, Estonia, Romania, Ukraine (Fig. +301 +). + + + +Diagnosis. + + +Fidiobia communis + +is close to + +F. hofferi + +because of its general habitus, the metascutellum that is visible in dorsal view and the presence of epitorular carinae. These two species differ mainly by the sculpture of the dorsal mesopleuron (reduced in + +F. hofferi + +and extending to the middle of the mesopleuron in + +F. communis + +), setation of the ventral metapleural area (few, sparse setae in + +F. hofferi + +and dense, long setae in + +F. communis + +) and the length of the marginal setae on the fore wings (very short, hardly visible in + +F. hofferi + +and clearly visible in + +F. communis + +). + + + + \ No newline at end of file diff --git a/data/38/B6/60/38B660D63CBDE466D85D00D6CE45F75B.xml b/data/38/B6/60/38B660D63CBDE466D85D00D6CE45F75B.xml new file mode 100644 index 00000000000..26df376e897 --- /dev/null +++ b/data/38/B6/60/38B660D63CBDE466D85D00D6CE45F75B.xml @@ -0,0 +1,177 @@ + + + +New record and redescription of Calanopiathompsoni A. Scott, 1909 (Copepoda, Calanoida, Pontellidae) from the Red Sea, with notes on the taxonomic status of C. parathompsoni Gaudy, 1969 and a key to species + + + +Author + +Al-Aidaroos, Ali M. + + + +Author + +Salama, Adnan J. + + + +Author + +El-Sherbiny, Mohsen M. + +text + + +ZooKeys + + +2016 + +552 + + +17 +32 + + + + +http://dx.doi.org/10.3897/zookeys.552.6180 + +journal article +http://dx.doi.org/10.3897/zookeys.552.6180 +1313-2970-552-17 +00F6AB4B7C444DC6914B827F8C5E278E + + + +Taxon classification Animalia Calanoida Pontellidae + + + +Calanopia thompsoni A. Scott, 1909 +Figs 1, 2, 3, 4, 5, 6, 7 + + + +Material examined. +Twelve adult females and ten adult males collected at Al-Wajh waters of the east coast of Saudi Arabian Red Sea. + + +Body length. + +Female 1.92-1.98 mm (mean ++/- +SD = 1.95 ++/- +0.02 mm, n = 12), male 1.79-1.83 mm (1.81 ++/- +0.01 mm, n = 10). + + + +Female. +Body robust (Fig. 1A), 1.94 mm in length. Prosome elliptical comprising cephalosome and four pedigerous somites, prosome approximately 2.5 times as long as urosome; cephalosome distinctly separated from first pediger with one median eye and lateral hooks; fourth and fifth pedigerous somites fused, symmetrical with posterolateral corners pointed in dorsal aspect reaching nearly one-third of way along genital compound somite (Fig. 2A). Rostrum bearing pair of pointed processes with very small medial subterminal notch (Figs 1B, C, 2B). Urosome (Figs 1A, B, 2A) of two free somites; genital compound somite symmetrical and ventral surface without any processes (Figs 1B, 2A). Second urosomite symmetrical and slightly shorter than genital compound somite. Caudal rami symmetrical and approximately 2.3 times as long as wide, each ramus carrying five plumose setae along distal margin and reduced seta (seta VII) located on dorsal surface near medial distal angle. + + +Figure 1. +Calanopia thompsoni +female from the Red Sea. A habitus, dorsal view B habitus, lateral view C rostrum, frontal view D antennule E enlarged proximal part of antennule F antenna. Scale bars in mm. + + + + +Figure 2. SEM micrograph of +Calanopia thompsoni +from the Red Sea. A female abdomen, lateral view B rostrum, lateral view C leg 5, ventral view D enlarged distal part of female leg 5. + + +Antennules (Fig. 1D, E) 19-segmented, when extended reaching almost anterior border of second urosomite. Armature formula as follows: ancestral segment I (segment 1) = 1 setae + aesthetasc (ae), II-VI (2) = 5 + 2 ae, VII (3) = 1 + ae, VIII-X (4) = 4 (1 spiniform) + ae, XI-XII (5) = 2 + ae, XIII (6) = 2 (1 spiniform) +ae, XIV (7) = 1 + ae, XV (8) = 1 + ae, XVI (9) = 2 + ae, XVII (10) = 2 + ae, XVIII (11) = 2 + ae, XIX (12) = 2 + ae, XX (13) = 2 + ae, XXI (14) = 2 +ae, XXII (15) = 1, XXIII (16) = 1, XXIV (17) = 1 + 1, XXV (18) = 1 + 1, XXVI-XXVIII (19) = 6 + ae. + +Antenna (Fig. 1F) biramous with short coxa bearing plumose seta at distomedial angle; basis with two subequal setae distomedially; exopod 5-segmented with setal formula of 0, 4, 1, 2, 3. Endopod 2-segmented, proximal segment with two unequal subterminal setae, distal segment bilobed, with medial (proximal) lobe bearing eight +setae +, and with lateral (distal) lobe crowned with six setae and transverse row of fine setules. + +Mandibular gnathobase (Fig. 3A) carrying eight teeth on coxal cutting edge, third to seventh teeth ornamented with row of short spinules anterodistally at base. Palp biramous; basis with four unequal setae on medial margin. Exopod 5-segmented with setal formula of 1, 1, 1, 1, 4. Endopod 2-segmented, proximal segment with two setae at distomedial corner, distal segment with seven long and one short setae. +Maxillule (Fig. 3B) with praecoxal arthrite bearing nine marginal strong spines and four setae on posterior surface. Coxal epipodite with nine setae; coxal endite with three setae, basal exite with one seta. Proximal and distal basal endites with three and one setae, respectively. Exopod carrying a total of nine setae; endopod incorporated into basis with three setae laterally and seven setae terminally. +Maxilla (Fig. 3C) praecoxal and coxal endites carrying 3 and 2, 2, 3 bilaterally spinulate setae respectively; basal endite with two setae, one longer than other; endopod 3-segmented, carrying six bilaterally spinulate setae. + + +Figure 3. +Calanopia thompsoni +female from the Red Sea. A mandible B maxillule C maxilla D maxilliped. Scale bars in mm. + + + +Maxilliped +(Fig. 3D) syncoxal lobes with 1, 3, 3 setae on their medial margins. Basis carrying two setae distally; endopod 4-segmented with setal formula of 2, 2, 1, 3. + + +Swimming +legs 1-4 (Fig. 4 +A-D +) biramous, with 3-segmented exopods and 2-segmented endopods. On leg 1 to leg 3, coxa with one medial seta and patch of fine hairs. All lateral spines on exopods of legs 1-4 with serrated hyaline margins. Leg 5 (Figs 2C, 4E) symmetrical, basis with short seta posteriorly; exopod 2-segmented, first segment with two strong bilaterally serrated processes laterally (distal one longer and pointed slightly mediad). Second exopod segment nearly as long as first one, bearing two bilaterally serrated, lateral spines, one small medial process fused to segment and bilaterally serrated long, distal spine fused to segment (Figs 2C, D, 4E). Armature of legs as follows: + + +Armature of legs + + + + + + + + + + + + + + + + +
CoxaBasisExopodEndopod
12312
+
+ + +Figure 4. +Calanopia thompsoni +female from the Red Sea. A leg 1 B leg 2 C leg 3 D leg 4 E leg 5. Scale bars in mm. + + + +Male +. Body (Fig. 5A, B) with plump prosome approximately 2.2 times as long as urosome comprising cephalosome and four pedigerous somites. Cephalosome distinctly separated from first pediger; fourth and fifth pedigerous fused and produced posterolaterally into symmetrical and slightly pointed corners reaching end of first urosomite (Figs 5A, 6A). Rostrum bearing pair of pointed processes directed posteroventrally (Fig. 5B). Urosome (Fig. 5A, B) comprising five free symmetrical urosomites, second urosomite longest; anal somite shorter preceding somite. Caudal rami symmetrical, 2.2 times longer than wide; caudal setae as in female. Some male specimens from Red Sea revealed the presence of one and/or two fine spinules, ventrally on the right side in the first and second urosomite respectively (Fig. 6A). + + + +Figure 5. +Calanopia thompsoni +male from the Red Sea. A habitus, dorsal view B habitus, lateral view C right antennule D enlarged proximal part of right antennule E antennule segments 12-14. Scale bars in mm. + + + + +Figure 6. SEM micrograph of +Calanopia thompsoni +from the Red Sea. A first and second male urosomite (spinules indicated by arrows), ventral view B distal segment of male left leg 5, ventral view C distal segment of male left leg 5, dorso-lateral view D exopod of male right leg 5. + + + +Right antennule (Fig. 5 +C-E +) 17-segmented, geniculate between segments XX (13) and XXI-XXIII (14). Armature as follows: ancestral segment I (segment 1) = 1 setae + aesthetasc (ae), II-V (2) = 6 + ae, VI-VII (3) = 5 + 3 ae, VIII (4) = 1 + ae, IX (5) = 2 + ae, X (6) = 1 + ae, XI (7) = 1 + ae, XII (8) = 2 + ae, XIII-XIV (9) = 3 + 2 ae, XV (10) = naked, XVI-XVII (11) = 3 (1 spiniform) + 2 ae, XVIII-XIX (12) = 2+ process + 2 ae, XX (13) = 1+ ae, XXI-XXIII (14) = 2 + 2 processes, XXIV (15) = 1 + 1, XXV (16) = 1+ ae + 1, XXVI-XXVIII (17) = 5 + ae. + +Left antennule, antenna, mouthparts and swimming legs 1-4 as in female. Leg 5 uniramous and asymmetrical. Left leg (Fig. 7A) with short coxa; basis 1.8 times longer than coxa with plumose seta located posteriorly near proximal end. Exopod 2-segmented, first (proximal) segment slightly shorter than basis with pointed attenuation near distolateral corner, second (distal) segment short, hirsute on posteromedial surface, with curved relatively long spine laterally, short spine with triangular base medially and one rounded and serrated process distally (Figs 6B, C, 7B, C). Right leg (Fig. 7D) longer than left, coxa with one blunt process on posterior surface distally; basis with plumose seta laterally. Exopod 2-segmented, forming a stout subchela, first exopodal segment without thumb and nearly 4 times as long as wide, distal part of subchela with elongate depression medially and one seta on proximal border of the depression (Figs 6D, 7D). Second exopodal segment (finger) elongate, curved at one-third its length, not acutely tapering with one medial seta proximally and two setae laterally nearly at midlength, distal part of finger with shallow depression medially. + + +Figure 7. +Calanopia thompsoni +male from the Red Sea. A left leg 5 B distal segment of left leg 5, ventral view C distal segment of left leg 5, dorso-lateral view D right leg 5. Scale bars in mm. + + +
+
+
\ No newline at end of file diff --git a/data/38/B6/F0/38B6F0D9BD2CF5FC561111036DD37C9D.xml b/data/38/B6/F0/38B6F0D9BD2CF5FC561111036DD37C9D.xml new file mode 100644 index 00000000000..68fd9cbb87c --- /dev/null +++ b/data/38/B6/F0/38B6F0D9BD2CF5FC561111036DD37C9D.xml @@ -0,0 +1,79 @@ + + + +Species plantarum: exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas + + + +Author + +Linnaeus, Carolus + +text + +1753 +Laurentius Salvius + +Stockholm + + + +https://doi.org/10.5962/bhl.title.669 + +book +10.5281/zenodo.3931989 +3931989 + + + + +Fritillaria meleagris +, +spec. nov. + + + + +5. Fritillaria foliis omnibus alternis. +Hort. ups. 81. + + +Fritillaria e foliorum alis florens. +Hort. cliff. 119. + + +Fritillaria radice depressa. +Roy. lugdb. 30. + + +Fritillaria praecox purpurea variegata. +Bauh. pin. 64. + + +Meleagris. +Reneal. spec. 147. t. 146. + + +β. Fritillaria alba variegata. +Bauh. pin. 64. + + +γ. Fritillaria alba praecox. +Bauh. pin. 64. + + +δ. Fritillaria serotina atropurpurea. +Bauh. pin. 64. + + + + +Habitat in +Gallia +, +Italia +. ♃ + + + + \ No newline at end of file diff --git a/data/38/B7/2E/38B72EC481356186ED75C00000130B3F.xml b/data/38/B7/2E/38B72EC481356186ED75C00000130B3F.xml new file mode 100644 index 00000000000..ac7ecf67f3e --- /dev/null +++ b/data/38/B7/2E/38B72EC481356186ED75C00000130B3F.xml @@ -0,0 +1,60 @@ + + + +Brazilian Trichoptera Checklist II + + + +Author + +Paprocki, Henrique + + + +Author + +Franca, Diogo + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1557 +1557 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1557 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1557 +1314-2828--1557 + + + + +Smicridea (Rhyacophylax) froehlichi Almeida & Flint, 2002 + + + +Distribution +Minas Gerais, Rio de Janeiro, Sao Paulo + + +Notes + +Almeida and Flint Jr 2002 +, +Dumas et al. 2010 + + + + \ No newline at end of file diff --git a/data/38/B7/5D/38B75DF511FF594CAF7CAA530A4D22C4.xml b/data/38/B7/5D/38B75DF511FF594CAF7CAA530A4D22C4.xml new file mode 100644 index 00000000000..e6f40445931 --- /dev/null +++ b/data/38/B7/5D/38B75DF511FF594CAF7CAA530A4D22C4.xml @@ -0,0 +1,101 @@ + + + +Bee species checklist of the San Francisco Peaks, Arizona + + + +Author + +McCabe, Lindsie M +Department of Biological Sciences, Northern Arizona University, Flagstaff, United States of America +https://orcid.org/0000-0001-9815-0581 +lma243@nau.edu + + + +Author + +Chesshire, Paige R +Department of Biological Sciences, Northern Arizona University, Flagstaff, United States of America + + + +Author + +Smith, David R +U. S. Fish and Wildlife Service, Southwest Forest Science Complex, Flagstaff, United States of America + + + +Author + +Wolf, Atticus +Department of Biological Sciences, Northern Arizona University, Flagstaff, United States of America + + + +Author + +Gibbs, Jason +Department of Entomology, University of Manitoba, Winnipeg, Canada +https://orcid.org/0000-0002-4945-5423 + + + +Author + +Griswold, Terry L +USDA-ARS, Pollinating Insects Research Unit, Logan, United States of America + + + +Author + +Wright, Karen W +Department of Entomology, Texas A & M, College Station, United States of America + + + +Author + +Cobb, Neil S +Department of Biological Sciences, Northern Arizona University, Flagstaff, United States of America +https://orcid.org/0000-0002-6155-9444 + +text + + +Biodiversity Data Journal + + +2020 + +8 + + +49285 +49285 + + + + +http://dx.doi.org/10.3897/BDJ.8.e49285 + +journal article +http://dx.doi.org/10.3897/BDJ.8.e49285 +1314-2828-8-e49285 +7B7852D5E053597D964773508EBDC88A + + + + +Megachile (Xanthosarus) perihirta Cockerell, 1898 + + + +Notes +Last collected on the Peaks in 1990 + + + \ No newline at end of file diff --git a/data/38/B7/E5/38B7E5677CB8321CB823EDB0920E80AE.xml b/data/38/B7/E5/38B7E5677CB8321CB823EDB0920E80AE.xml new file mode 100644 index 00000000000..36124d26014 --- /dev/null +++ b/data/38/B7/E5/38B7E5677CB8321CB823EDB0920E80AE.xml @@ -0,0 +1,112 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part V) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +911 +926 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Vinca major +Linnaeus + +, + +Species Plantarum +1 + +: 209. 1753 + + +. + + + +"Habitat in Gallia Narbonensi, Hispania." RCN: 1712. + + + + +Lectotype +(Stearn in Taylor & Farnsworth, + +Vinca +Alkaloids + +: 79. 1973): Herb. Linn. No. 299.3 ( +LINN +) + +. + + + + +Current name: + + +Vinca major + +L. + +( +Apocynaceae +). + + + + + +Note: +Vinca major + +was treated as the +generitype +by Britton & Brown ( +Ill. Fl. N. U. S. +, ed. 2, 3: 20. 1913). However, under Art. 10.5, Ex. 7 (a voted example) of the Vienna Code, this is a type choice made under the American Code and is to be replaced under Art. 10.5b by +Hitchcock's +choice ( +Prop. Brit. Bot. +: 136. 1929) of + +V minor +L. + + + + + \ No newline at end of file diff --git a/data/38/B7/F7/38B7F719A18768A41D168C5707098FC2.xml b/data/38/B7/F7/38B7F719A18768A41D168C5707098FC2.xml new file mode 100644 index 00000000000..ae4f2ff37f6 --- /dev/null +++ b/data/38/B7/F7/38B7F719A18768A41D168C5707098FC2.xml @@ -0,0 +1,173 @@ + + + +Cryptic species diversity in polypores: the Skeletocutisnivea species complex + + + +Author + +Korhonen, Aku + + + +Author + +Seelan, Jaya Seelan Sathiya + + + +Author + +Miettinen, Otto + +text + + +MycoKeys + + +2018 + +36 + + +45 +82 + + + + +http://dx.doi.org/10.3897/mycokeys.36.27002 + +journal article +http://dx.doi.org/10.3897/mycokeys.36.27002 +1314-4049-36-45 + + + + +Skeletocutis coprosmae (G. Cunn.) A. Korhonen & Miettinen +comb. nov. + + + +Basionym. + +Poria coprosmae +G. Cunn., Bulletin of the New Zealand Department of Industrial Research 72: 38 (1947). + + + +Holotype. + +New Zealand. Westland: Lake Mapourika, +Coprosma +, Nov 1946 J.M.Dingley (PDD 5252, studied). + + + +Description. + +Basidiocarps possibly perennial; resupinate to half-resupinate; up to 6 cm wide and 8 mm thick; hard when dry, breaking apart neatly; pilei fleshy, protruding up to 1.7 cm; margin blunt with narrow, sterile ridge on the underside; upper surface minutely rough, matted, white to cream coloured when young, turning ochraceous brown and finally blackish with age; pore surface sometimes with greenish-grey tints deep within the tubes in pileate part; context and subiculum whitish-cream colour to light greyish-brown near contact with substrate (in thick basidiocarps); context up to 5 mm thick, azonate; tube layer from 0.5-1.5 up to 6 mm thick and zonate in perennial basidiocarp, lighter horizontal zones appear where tubes are filled with arbuscule-like 'binding +hyphae' +; pores (6 +-)7-8(- +9) per mm. + + +Hyphal structure: skeletal hyphae in context 2.0-4.3(-5.3) +µm +wide, in subiculum (1.0 +-)2.0-3.5(- +4.2) +µm +wide, in trama 2.0 +-4.0(- +5.0) +µm +wide, generative hyphae in trama 1.0 +-2.3(- +3.0) +µm +wide. + + +Basidiospores 2.8 +-3.2(-3.3)x0.5- +0.7 +µm +, L=2.98 +µm +, W=0.57 +µm +, +Q'=(4.0-)4.3-6.0(- +6.4), Q=5.19, n=60/2. + + + +Distribution and ecology. +Available material is very limited but suggests a rather wide, temperate Australasian distribution from Tasmania to southern New Zealand. + + +Specimens examined. +AUSTRALIA. Tasmania: Huon Valley, indet. angiosperm wood, 21 Nov 2006 Gates 1898 (H). NEW ZEALAND. Westland: (holotype, see above). + + +Discussion. + +After examining the type, we have chosen to use a previously published name +Poria coprosmae +as the basionym for this Australasian species. +P. coprosmae +was described by +Cunningham (1947) +from Westland, New Zealand. He ( +Cunningham 1965 +) later concluded that his +P. coprosmae +was the same as +Polyporus semipileatus +Peck but he treated them mistakenly under the name +Tyromyces chioneus +(Fr.) P. Karst., as explained by +Buchanan and Ryvarden (1988) +. + + +In their type studies of +Polyporaceae +species described by Cunningham, +Buchanan and Ryvarden (1988) +place +P. coprosmae +in the genus +Ceriporiopsis +Dom., rejecting placement in +Incrustoporia +or +Skeletocutis +based on the absence of encrusted hyphae. +Rajchenberg (1995) +, on the other hand, found the hyphal structure in the holotype and other collections of +P. coprosmae +in PDD more in line with that of +S. nivea +. Our studies of the holotype confirm this view with the addition that we also observed encrusted generocystidia and thin-walled skeletal hyphae in the trama, which are characteristic for the +S. nivea +complex. Macroscopically, the only other studied specimen from Tasmania looks quite different from the type. However, we could not identify any clear microscopic differences and cannot rule out the possibility that the macroscopic differences represent variation between developmental stages. Nevertheless, considering the level of crypticity in the +S. nivea +complex, we have reservations in stating that our sequenced specimens are truly conspecific with the old type. Thus, we refrain from assigning an epitype for now. + + +S. nivea +occurs in the North Island of New Zealand and it is possible that these two species could overlap as +S. nivea +has been shown to extend respectively far into the temperate zone in the northern hemisphere. The type specimen is a thin and resupinate basidiocarp on a fallen branch of a +Coprosma +shrub. The Tasmanian specimen, on the other hand, has evidently been growing on coarse wood and is unique in having a clearly perennial habit with a zonate tube layer. + + + + \ No newline at end of file diff --git a/data/38/B8/21/38B82188630C55DA81D90EA3CD67F95D.xml b/data/38/B8/21/38B82188630C55DA81D90EA3CD67F95D.xml new file mode 100644 index 00000000000..c7cb110a438 --- /dev/null +++ b/data/38/B8/21/38B82188630C55DA81D90EA3CD67F95D.xml @@ -0,0 +1,194 @@ + + + +Molecular data resolving the systematics of the related Blattellidae genera Symploce, Episymploce, and Blattella (Blattodea: Blaberoidea) + + + +Author + +Jin, Duting +College of Plant Protection, Southwest University, Beibei, Chongqing 400715, China + + + +Author + +Zhao, Qiongyao +College of Plant Protection, Southwest University, Beibei, Chongqing 400715, China + + + +Author + +Han, Wei +College of Plant Protection, Southwest University, Beibei, Chongqing 400715, China + + + +Author + +Li, Jinxiang +College of Plant Protection, Southwest University, Beibei, Chongqing 400715, China + + + +Author + +Wang, Zongqing +College of Plant Protection, Southwest University, Beibei, Chongqing 400715, China + + + +Author + +Che, Yanli +College of Plant Protection, Southwest University, Beibei, Chongqing 400715, China +shirleyche2000@126.com + +text + + +Arthropod Systematics & amp; Phylogeny + + +2022 + +2022-05-31 + + +80 + + +187 +208 + + + + +http://dx.doi.org/10.3897/asp.80.e62469 + +journal article +http://dx.doi.org/10.3897/asp.80.e62469 +1864-8312-80-187 +7CF10F11BCDC4421A43357CFB018EE52 +06122163C48155A6BD2D650FD473B6DB + + + + +3.2.12. +Episymploce kunmingi (Bey-Bienko, 1969) + + + + +Symploce kunmingi +Bey-Bienko, 1969: 855 (Type locality: Yunnan, China). + + +Episymploce kunmingi +: Roth, 1985b, 215. + + +Symploce quadrispinis +Woo and Feng, 1992: 54 (Type locality: Yunnan, China) +syn. nov. + + + +Material examined. + + +CHINA +• +1 ♂ +( +holotype +of + +S. quadrispinis + +); +Yunnan Prov. +, +Lushui City +, +Liuku Town +, +12 June 1981 +, +Jianmin Zhao +leg. + +• + +1 ♂ +, +1 ♀ +; +Yunnan Prov. +, +Kunming City +; +13 June 1986 +; +Pingzhang Feng +leg. + +• + +1 ♂ +, +1 ♀ +; +Sichuan Prov. +, +Leshan City +, +Jinhekou County +; +26-27 May 2011 +, +Keliang Wu +leg. + + + + +Remarks. + + +Episymploce kunmingi + +was published by Bey-Bienko in + +Symploce + +and was transferred to + +Episymploce + +by +Roth (1985b) +based on the asymmetric T10. After examination of + +Episymploce kunmingi + +(Bey-Bienko, 1969) and comparison with the holotype of + +Symploce quadrispinis + +Woo and Feng, 1992, we found that there was no difference in their external morphology and male genitalia. So we regard + +Symploce quadrispinis + +as a synonym of + +Episymploce kunmingi + +(Bey-Bienko, 1969). + + + + \ No newline at end of file diff --git a/data/38/B8/7F/38B87F4F92AC1A947A2445AEEC8DF8E1.xml b/data/38/B8/7F/38B87F4F92AC1A947A2445AEEC8DF8E1.xml new file mode 100644 index 00000000000..0d4d9e3eddc --- /dev/null +++ b/data/38/B8/7F/38B87F4F92AC1A947A2445AEEC8DF8E1.xml @@ -0,0 +1,53 @@ + + + +The Formicidae (Hymenoptera) of Fennoscandia and Denmark. + + + +Author + +Collingwood, C. A. + +text + + +Fauna Entomologica Scandinavica + + +1979 + +8 + + +1 +174 + + + + +http://antbase.org/ants/publications/6175/6175.pdf + +journal article +6175 + + + + +Lasius distinguendus +(Emery, 1916:64) + + + + +This is an inadequately characterised species. It is mainly found in South and Central Europe and most easily recognised in the queen caste. It is like a larger, paler +L. mixtus +but has more abundant genal hairs and a high broadly emarginate scale. The worker has occasional tibial hairs and longer body hairs than +L. mixtus +and would be more easily confused with +L. umbratus +. According to B. Pisarski (priv.commun.) it occurs in North Germany and probably also in Poland. + + + + \ No newline at end of file diff --git a/data/38/B8/8F/38B88F1595655863A262EAA792C67AC3.xml b/data/38/B8/8F/38B88F1595655863A262EAA792C67AC3.xml new file mode 100644 index 00000000000..b646ddf78f9 --- /dev/null +++ b/data/38/B8/8F/38B88F1595655863A262EAA792C67AC3.xml @@ -0,0 +1,122 @@ + + + +Distribution of wild bee (Hymenoptera: Anthophila) and hoverfly (Diptera: Syrphidae) communities within farms undergoing ecological transition + + + +Author + +Noel, Gregoire +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium +gregoire.noel@uliege.be + + + +Author + +Bonnet, Julie +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + + + +Author + +Everaerts, Sylvain +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + + + +Author + +Danel, Anouk +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + + + +Author + +Calderan, Alix +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + + + +Author + +de Liedekerke, Alexis +Ferme de Froidefontaine, Havelange, Belgium + + + +Author + +de Montpellier d'Annevoie, Clotilde +Department of Geography, Institute Transitions, University of Namur, Namur, Belgium & Ferme d'Emeville, Havelange, Belgium + + + +Author + +Francis, Frederic +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + + + +Author + +Serteyn, Laurent +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + +text + + +Biodiversity Data Journal + + +2021 + +2021-01-14 + + +9 + + +60665 +60665 + + + + +http://dx.doi.org/10.3897/BDJ.9.e60665 + +journal article +http://dx.doi.org/10.3897/BDJ.9.e60665 +1314-2828-9-e60665 +A14A82B6E4E456E6AA051CADA0ECE3E6 + + + + +Eristalis tenax (Linnaeus 1758) + + + +Ecological interactions + + +Feeds on +Polylectic + + +Conservation status +Not Applicable + + +Notes + +Table +2 + + + + \ No newline at end of file diff --git a/data/38/B8/F1/38B8F1D2E85450E895C476D2A6D0DD01.xml b/data/38/B8/F1/38B8F1D2E85450E895C476D2A6D0DD01.xml new file mode 100644 index 00000000000..72c82f0f8a9 --- /dev/null +++ b/data/38/B8/F1/38B8F1D2E85450E895C476D2A6D0DD01.xml @@ -0,0 +1,990 @@ + + + +The taeniaticornis - group of genus Apanteles Foerster (Hymenoptera, Braconidae, Microgastrinae) from China with one new species + + + +Author + +Liu, Zhen +Zoology Key Laboratory of Hunan Higher Education, College of Life and Environmental Sciences, Hunan University of Arts and Science, Changde 415000, China & Institute of Insect Sciences, Zhejiang University, Hangzhou 310058, China +qingniao8.27@163.com + + + +Author + +Chen, Xue-xin +https://orcid.org/0000-0002-9109-8853 +Institute of Insect Sciences, Zhejiang University, Hangzhou 310058, China + +text + + +Journal of Hymenoptera Research + + +2023 + +2023-03-16 + + +96 + + +21 +31 + + + + +http://dx.doi.org/10.3897/jhr.96.99649 + +journal article +http://dx.doi.org/10.3897/jhr.96.99649 +1314-2607-96-21 +75406EC011914095B443C5313C1BA1C0 +68A5E663F8F65810A6C8055516734896 + + + + +Apanteles conon Nixon, 1965 + + + + +Fig. 1 + + + + +Apanteles conon +Nixon, 1965: 124. Type in Natural History Museum, London. Chen et Song 2004: 38. + + + +Diagnosis. + +Vertex between the eye and the posterior ocellus shiny with superficial fine punctures; ocelli big, posterior imaginary tangent to fore ocellus transecting the posterior pair; antenna slightly longer than body length, with penultimate antennomere 1.4 +x +longer than wide; punctures on mesoscutum coarse, interspaces not bigger than their diameter, punctures indistinctly confluent above the hind polished area; areola on propodeum open anteriorly, V-shaped apically, with strong costulae, three posterior fields smooth without carinae; pterostigma big, 2.3 +x +as long as its widest part, vein 1-R1 1.5 +x +longer than pterostigma, 7.5 +x +as long as its distance from the apex of the marginal cell, r 2.4 +x +longer than 2-SR, angled at their meeting; T1 strongly wedged-shaped, 4.6 +x +longer than hind width, turned-over part with rugose punctures laterally, T3 2 +x +as long as T2; legs mostly yellow, hind coxa brown; ovipositor sheath about as long as hind tibia. + + + +Figure 1. + +Apanteles conon + +Nixon, 1965 +a +habitus, lateral view +b +head, dorsal view +c +head, frontal view +d +mesosoma, dorsal view +e +propodeum +f +mesopleuron +g +fore wing +h +abdomen, dorsal view. Scale bars: 0.5 mm. + + + + +Variation. +Body length 3.0-3.2 mm. + + +Male. + +Similar to female, except for antenna distinctly longer than body length, penultimate antennomere 2 +x +longer than wide, and T2 higher. + + + +Host. +Unknown. + + +Material examined. + +ZJUH +: + +1♀ +, +Shaxian +, + +Fujian + +, 1980.XII, +Gong Weili +, +No. +810003 + +; + +4♀♀ +, +Mt. Wuyi +, +Fujian +, +1988.IX.7 +, +Lin Changfu +, +Nos. +20005691, 20005687, 20005692, 20005700 + +; + +1♀ +, +Mt. Wuyi +, +Fujian +, +1989.XI.1 +, +Wang Jiashe +, +No. +964568 + +; + +1♀ +, +Chibi +, +Yongqin +, +Fujian +, +2002.IX.17 +, +Liu Jinxian +, +No. +20023635 + +; + +2♀♀ +, +Dazhulan +, +Fujian +, +1991.X.6 +, +Chen Xuexin +, +Nos. +920343, 920354 + +; + +2♀♀ +, +Qingliu +, +Fujian +, +1986.VI.20 +, +Qi Shicheng +, +Nos. +965199, 9651200 + +; + +1♀ +, +Antongmu +, +Fujian +, +1981.IX.29 +, +Fei Juyi +, +No. +20004167 + +; + +2♀♀ +, +Mt. Longxi +, +Jiangle +, +Fujian +, +1991.VII.16 +/IX.30, +Liu Changming +, +Nos. +20007164, 20007209 + +; + +3♀♀ +2♂♂ +, +Mt. Wuyi +( +Tongmucun +), +Fujian +, +2009.IV.17 +/15, +Wang Manman +, +Nos. +200900409, 200900398, 200900411, 200900408, 200900545 + +; + +6♂♂ +, +Mt. Wuyi +( +Qili +), +Fujian +, +2009.IV.18 +, +Zeng Jie +, +Nos. +200900618, 200900650, 200900639, 200900647, 200900646, 200900642 + +; + +1♂ +, +Mt. Wuyi +( +Sangang +), +Fujian +, +2009.IV.17 +, +Zeng Jie +, +No. +200900481 + +; + +1♂ +, +Mt. Wuyi +( +Pikeng +), +Fujian +, +2009.IV.21 +, +Zeng Jie +, +No. +200900503 + +; + +1♂ +, +Sangang +, +Fujian +, +1981.V.6 +, +Han Ying +, +No. +20003920 + +; + +1♂ +, +Guanxian +, + +Sichuan + +, +1980.VIII.1 +, +He Junhua +, +No. +803037 + +; + +1♀ +, +Hangzhou +, + +Zhejiang + +, 1981, +Lou Xiaoming +, +No. +930324 + +; + +1♀ +, +Mt. Tianmu +, +Zhejiang +, +1987.VII.21 +, +Lou Xiaoming +, +No. +874572 + +; + +2♀♀ +, +Mt. Fengyang +, +Longquan +, +Zhejiang +, +2003.VIII.7 +/10, +Liu Jingxian +, +Nos. +20055581, 20048319 + +; + +1♀ +, +Mt. Jiulong +, +Suichang +, +Zhejiang +, +1994.VIII.18 +, +Can Ping +, +No. +944261 + +; + +2♀♀ +, +Mt. Longwang +, +Anji +, +Zhejiang +, +1996.VI.26 +, +Zhao Weichun +, +Nos. +963915, 963916 + +; + +1♀ +, +Mt. Jiulong +, +Suichang +, +Zhejiang +, +1993.VIII.31 +, +Chen Xuexin +, +No. +939685 + +; + +1♀ +, +Mt. Tianmu +( +Jinshanmen +), +Zhejiang +, +1999.VIII.6 +, +Zhao Mingshui +, +No. +20002876 + +; + +4♀♀ +, +Hangzhou +, +Zhejiang +, +1989.VI.24 +/XI.10, +He Junhua +, +Nos. +893118, 893108, 893311, 896960 + +; + +2♀♀ +, +Liuheta +, +Hangzhou +, +Zhejiang +, +2001.V.19 +, +Piao Meihua +, +Nos. +200702186, 200702187 + +; + +1♀ +, +Songyang +, +Zhejiang +, +1992.XI.1-XII.9 +, +Chen Hanlin +, +No. +934062 + +; + +1♀ +, +Hangzhou +, +Zhejiang +, +1991.V.28 +, +He Junhua +, +No. +911118 + +; + +1♂ +, +Mt. Tianmu +( +Xianrending +), +Zhejiang +, +2011.VII.25-29 +, +Liu Zhen +, +No. +201102651 + +; + +1♀ +, +Mt. Tai +, +Taian +, + +Shandong + +, +1997.VII.17 +, +Chen Xuexin +, +No. +974014 + +; + +1♀ +, +Yuexi +, + +Anhui + +, +1981.V.16 +, +Yang Fuan +, +No. +820593 + +; + +1♀ +, +Shenlongjia +( +Honghua +, + +900m + +), + +Hubei + +, +1982.VIII.25 +, +He Junhua +, +No. +825390 + +; + +1♀ +, +Mengxiu +, +Ruili +, + +Yunnan + +, +1981.V.2-6 +, +He Junhua +, +No. +812956 + +; + +1♀ +, +Jianfengling +, + +Hainan + +, +2007.VI.7 +, +Liu Jinxian +, +No. +200702381 + +; + +1♀ +, +Meitan +, + +Guizhou + +, +1982.VI.2 +, +Xia Huaien +, +No. +824620 + +; + +1♀ +, +Fengxi +, +Meizhou +, + +Guangdong + +, +2003.VII.29 +, +Chen Jujian +, +No. +20048632 + +; + +1♀ +, +Mt +, +Yunji +, +Xinfeng +, +Guangdong +, +2003.VII.20 +, +Li Ping +, +No. +20053969 + +; + +1♀ +, +Fengkai +, +Guangdong +, +1992.V.16 +, +Ma Yun +, +No. +921135 + +; + +3♀♀ +, +Nanling +, +Fuyuan +, +Guangdong +, +2004.V.8 +/ +2003.VII.23 +, +Xu Zaifu +, +Nos. +20049641, 20049592, 20049143 + +; + +2♂♂ +, +Dianba +( + +900m + +), +Wenxian +, + +Gansu + +, +1998.VI.16 +, +Ma Yun +, +Nos. +984241, 984332 + +; + +1♂ +, +Yingtaogou +, +Xiangshan +, + +Beijing + +, +1992.VII.6 +, +Lin Naiquan +, +No. +20004394 + +; + +5♂♂ +, +Shouka +, + +Taiwan + +, +2011.V.30 +, +Tang Pu +, +Nos. +201105461, 201105456, 201105455, 201105483, 201105454 + +; + +1♂ +, +Mt. Dongmao +, +Taiwan +, +2011.VI.4 +, +Tangpu +, +No. +201104500 + +; + +1♂ +, +Mt. Beishou +, +Gaoxiong +, +Taiwan +, +2011.V.29 +, +Tang Pu +, +No. +201104487 + +; + +2♂♂ +, +Duonalindao +, +Taiwan +, +2011.VI.13 +, +Tang Pu +, +Nos. +201104994, 201104953 + +; + +9♂♂ +, +Mt. Wugong +, +Gaoxiong +, +Taiwan +, +2011.VI.15 +, +Tang Pu +, +Nos. +201104826, 201104837, 201104838, 201104844, 201104846, 201104847, 201104855, 201104821, 201104827 + +; + +1♂ +, +Mt. +Nantou +, +Taiwan +, +2011.VI.19 +, +Tang Pu +, +No. +201104794 + +; + + +HUAS +: + +1♀ +, +Bawangling +, + +Hainan + +( +malaise trap +), +2020.IX.30-X.30 +, +Chen Longlong +, +No. +202203542 + +; + +1♀ +, +Mt. Limu +, +Qiongzhong +, +Hainan +( +malaise trap +), +2020.IX.30-X.31 +, +Chen Longlong +, +No. +202201705 + +; + +1♀ +, +Haizhu Wetland +, +Guangzhou +, + +Guangdong + +( +malaise trap +), +2021.III.20-IV.5 +, +Liu Jingxian +, +No. +202200412 + +; + +8♀♀ +, +Haizhu Wetland +, +Guangzhou +, +Guangdong +( +malaise trap +), +2021.IV.26-V.11 +, +Liu Jingxian +, +Nos. +202200200, 202200204, 202200226, 202200237, 202200263, 202200269, 202200274, 202200290 + +. + + + +Distribution. +China (Anhui, Beijing, Fujian, Gansu, Guangdong, Guizhou, Hainan, Hubei, Hunan, Shandong, Sichuan, Taiwan, Yunnan, Zhejiang); Indonesia; Korea; Philippines. + + +Notes. + +Fernandez et al. (2020) examined the holotype in Natural History Museum, noting + +A. conon + +is possible a + +Dolichogenidea + +species because the punctures near the scutellar sulcus on mesoscutum do not fuse, but they kept it in + +Apanteles + +because other characters were invisible (such as setae beyond the widest part of vannal lobe). We had no opportunity to check the type, but checked the original description (Nixon, 1965), detailed examination from +Chen and Song (2004) +and +Papp (1974) +and characters from Chinese specimens (the typical wedged shaped T1). We also favor its placement in the genus + +Apanteles + +. + + + + \ No newline at end of file diff --git a/data/38/B9/29/38B929D4229FE8E1CE3C66A7BB75BE45.xml b/data/38/B9/29/38B929D4229FE8E1CE3C66A7BB75BE45.xml new file mode 100644 index 00000000000..14e9259873d --- /dev/null +++ b/data/38/B9/29/38B929D4229FE8E1CE3C66A7BB75BE45.xml @@ -0,0 +1,77 @@ + + + +Order Chiroptera - Family Vespertilionidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +451 +529 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Miniopterus inflatus +subsp. +inflatus +Thomas 1903 + + + + + + + +Miniopterus inflatus +subsp. +inflatus +Thomas 1903 + +, +Ann. Mag. Nat. Hist., ser. 7, 12: 634 + +. + + + + +Type Locality: + +Cameroon +, Efulen. + + + + + \ No newline at end of file diff --git a/data/38/BA/FF/38BAFFF62D643C4BD81887F58B93D7F8.xml b/data/38/BA/FF/38BAFFF62D643C4BD81887F58B93D7F8.xml new file mode 100644 index 00000000000..a73c1563a78 --- /dev/null +++ b/data/38/BA/FF/38BAFFF62D643C4BD81887F58B93D7F8.xml @@ -0,0 +1,42 @@ + + + +Catalogue of the hymenopterous insects in the collection of the British Museum. Part VI. Formicidae. + + + +Author + +Smith, F. + +text + +1858 +British Museum + +London + + + +http://antbase.org/ants/publications/8127/8127.pdf + +book +8127 +C86CFDBF-61D9-48EE-9C2E-325FC0462B10 + + + + +46. +Polyrhachis viscosus +. Pl. IV. fig. 41. B.M. + + + +Worker. Length 2 1/4 lines.-Opake-black: head and thorax finely rugose, abdomen delicately shagreened. The thorax with a short, stout, acute tooth at each of its anterior angles, and also a minute one at the posterior angles of the metathorax; the divisions of the parts of the thorax strongly marked, the disk slightly convex, with the lateral margins acute. The scale of the peduncle incrassate, subquadrate, with a long, acute spine at each of the superior angles, and two shorter ones between them. Abdomen subglobose. + + +Hab. Port Natal. + + + \ No newline at end of file diff --git a/data/38/BB/34/38BB3487B122B109BCE6AC721D8379F7.xml b/data/38/BB/34/38BB3487B122B109BCE6AC721D8379F7.xml new file mode 100644 index 00000000000..9b29e0daa91 --- /dev/null +++ b/data/38/BB/34/38BB3487B122B109BCE6AC721D8379F7.xml @@ -0,0 +1,71 @@ + + + +Cyanobacteria of Greece: an annotated checklist + + + +Author + +Gkelis, Spyros + + + +Author + +Ourailidis, Iordanis + + + +Author + +Panou, Manthos + + + +Author + +Pappas, Nikos + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +10084 +10084 + + + + +http://dx.doi.org/10.3897/BDJ.4.e10084 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e10084 +1314-2828--10084 + + + + +Schizothrix calcicola Gomont, 1892 + + + + +Schizothrix calcicola + + + +Notes + +Anagnostidis 1968 + + + + \ No newline at end of file diff --git a/data/38/BB/9D/38BB9D0D5A4B477B5A271FA5FD5C486B.xml b/data/38/BB/9D/38BB9D0D5A4B477B5A271FA5FD5C486B.xml new file mode 100644 index 00000000000..aa8971071a4 --- /dev/null +++ b/data/38/BB/9D/38BB9D0D5A4B477B5A271FA5FD5C486B.xml @@ -0,0 +1,259 @@ + + + +Contribution to knowledge of the genus Chydaeus in Xizang Autonomous Region [Tibet] and Yunnan Province, China (Coleoptera, Carabidae, Harpalini) + + + +Author + +Kataev, Boris M. +Zoological Institute, Russian Academy of Sciences, Universitetskaya nab. 1, St. Petersburg 199034, Russia + + + +Author + +Liang, Hongbin +Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China + + + +Author + +Kavanaugh, David H. +Department of Entomology, California Academy of Sciences, San Francisco, California 94118 USA +dkavanaugh@calacademy.org + +text + + +ZooKeys + + +2012 + +2012-02-24 + + +171 + + +39 +92 + + + + +http://dx.doi.org/10.3897/zookeys.171.2306 + +journal article +http://dx.doi.org/10.3897/zookeys.171.2306 +1313-2970-171-39 +1C0AE742AF194DCE8A6E86B6D72ECCB2 +F3103053C45BFFED2A35FFF7FFA5FFA6 +576907 + + + + +Chydaeus convexus Ito, 2002 +Figs 58 +70 + + + +Material examined. + +A total of 125 specimens (71 males and 54 females, including 35 males and 26 females in CAS, 35 males and 27 females in IOZ, and 1 male and 1 female in ZIN) were examined from the following localities: +China +. +Yunnan Province +. + +Longling County + +: 1 female, Longjiang, Xiaoheishan, tree & log, +24.83696°N +, +98.75735°E +, 2120 m, 27.V.2005, H.B. Liang & J.L Yang leg. (IOZ); 1 male, same data, but riverside, +24.82886°N +, +98.75917°E +, 2010 m, 25.V.2005, H.B. Liang leg. (IOZ); 3 males, 1 female, same data, but roadside, +24.82888°N +, +98.76001°E +, 2020 m, 28.V.2005, D. Kavanaugh & D.Z. Dong leg. (CAS); 2 female, same data, but riverside, 26.V.2005, D. Kavanaugh leg. (CAS). +Longyang County (District) +: 1 female, Bawan, 34 km from Bawan on Tengchong Road, 2310 m, +24.92944°N +, +98.75917°E +, 16.X.2003, D.Z. Dong leg. (IOZ); 1 male, Bawan, Luokeng, 41 km on road to Tengchong, +24°56'23.2"N +, +98°45'11.6"E +, 2440 m, 15.X.2003, day, H.-B. +Liang +& X.C. Shi leg. (IOZ); 1 female, Bawan, 41 km on old road to Tengchong, +25°56'15.0"N +, +98°45'02.8"E +, 2486 m, 11.X.2003, H.B. Liang leg. (IOZ); 1 male, Gaoligong Shan, Baoshan Pref., Nankang Yakou, +24°49.9'N +, +98°46.0'E +, 2130 m, 4-7 IX.1998, Stop 98-129A, D. Kavanaugh, C.E. Griswold, C.L. Long, R. Li & H.-X. He leg. (CAS); 1 male, same data as preceding (IOZ); 1 female, same data, but +24.81944°N +, +98.77111°E +, 2130 m, 27.X.2003, D.Z. Dong leg. (IOZ); 1 male,1 female, Bawan Town, Nankang Yakou, roadside, +24°49'33.4"N +, +98°46'20.0"E +, 2130 m, 26.X.2003, H.B. Liang & X.C. Shi leg. (IOZ); 1 male, 6 females, same data, but +24.81944°N +, +98.77111°E +, 2130 m, 31.X.2003, D.Z. Dong leg. (CAS, IOZ); 5 males, 4 females, Bawan Town, Nankang forest station, +24°49'28.8"N +, +98°46'43.6"E +, 2085 m, 27.X.2003, H.B. Liang & X.C. Shi leg. (CAS, IOZ); 1 female, Bawan, Nankang station, +24.82614°N +, +98.77602°E +, 1900 m, 26.V.2005, D.Z. Dong leg. (IOZ); 1 female, same data, but +24.83178°N +, +98.76462°E +, 2180 m, 22.V.2005, D. Kavanaugh & D.Z. Dong leg. (CAS); 6 males, 4 females, Bawan, 36-37 km on old road to Tengchong, +24°56'03.3"N +, +98°46'46.4"E +, 2150 m, 12.X.2003, H.B. Liang & X.C. Shi leg. CAS, IOZ); 1 male, 3 females, Bawan, Bawan - Tengchong Road km 29-35, 2000-2350 m, +24.92916°N +, +98.75861°E +, 12.X.2003, D.Z. Dong leg. (CAS, IOZ); 1 male, 4 females, Bawan, Yakou to Sanchawa, along road, +24°56'50.5"N +, +98°45'20.0"E +, 2300 m, 13.X.2003, H.B. Liang & X.C. Li leg. (CAS, IOZ); 4 males, Bawan, Dasheyao forest station - Yakou, +24°55'37.4"N +, +98°45'09.8"E +, 2404 m, 12.X.2003, H.B. Liang & X.C. Shi leg. (CAS, IOZ); 1 male, 2 females, Bawan, Dasheyao, +24.92989°N +, +98.75862°E +, 2320 m, 1.VI.2005, Dao Zhilong leg. (CAS, IOZ); 2 males, same data, but +24.92994°N +, +98.75850°E +, 2300 m, 3.VI.2005, D. Kavanaugh & D.Z. Dong leg. (CAS, IOZ); 2 males, 2 females, Bawan, Nankang station, +24.82260°N +, +98.78201°E +, 2060 m, 23.V.2005, H.B. Liang leg. (CAS, IOZ); 1 male, same data, but +24.82600°N +, +98.77690°E +, 2090 m, 28.V.2005, D. Kavanaugh leg. (CAS); 1 female, same data, but +24.82587°N +, +98.76832°E +, 2048 m, 22.V.2005, H.B. Liang leg. (IOZ); 1 female, same data, but +24.83178°N +, +98.76462°E +, 2180 m, 22.V.2005, D. Kavanaugh & D.Z. Dong leg. (CAS); 1 female, same data, but +24.82614°N +, +98.77602°E +, 1900 m, 26.V.2005, D.Z. Dong leg. (IOZ); 2 males, Bawan, Luoshuidong, 2300-2480 m, +24.93278°N +, +98.75333°E +, 13.X.2003, D.Z. Dong leg. (CAS, IOZ); 11 males, 4 females, Bawan, Sanchahe, +24.94755°N +, +98.75564°E +, 2300 m, 3.VI.2005, H.B. Liang & H.M. Yan leg. (CAS, IOZ); 4 males, same data, but +24.94865°N +, +98.75193°E +, 2350 m, 30.V.2005, H.B. Liang leg. (CAS, IOZ); 1 male, same data, but 2300 m, +24.94849°N +, +98.75699°E +, 30.V.2005, D. Kavanaugh leg. (IOZ); 2 males, 2 females, same data, but 3.VI.2003, D. Kavanaugh & D.Z. Dong leg. (CAS, IOZ); 1 female, same data, but D.Z. Dong leg. (IOZ). +Tengchong County +: 1 male, Jietou, Datang, Dahetou, +25.69700°N +, +98.68059°E +, 1800-2000 m, 16.VI.2005, Huang Hao leg. (IOZ); 8 males, 6 females, Dahaoping, 46-51 km on old road, +24°57'25.6"N +, +98°44'12.3"E +, 2220 m, 17.X.2003, H.B. Liang & X.C. Shi leg. (IOZ, ZIN); 2 males, Dahaoping, 43 km from Bawan on Tengchong Road, 2410 m, +24.95361°N +, +98.73333°E +, 14.X.2003, D.Z. Dong leg. (IOZ); 3 males, 3 females, Dahaoping, along a small stream, +24°58'20.8"N +, +98°44'20.1"E +, 2170 m, 18.X.2003, H.B. Liang & X.C. Shi +leg +. (CAS, IOZ); 1 male, Shangying, 5-8 km E of Dahaoping, 2358 m, +24.93417°N +, +98.74750°E +, 18.X.2003, D.Z. Dong leg. (IOZ); 4 males, Shangying, 42-46 km on road from Bawan, +24°57'13.0"N +, +98°44'32.1"E +, 2290 m, 14.X.2003, H.B. Liang & X.C. Shi leg. (CAS, IOZ); 1 male, Shangying, Longjiang bridge, riverside, +25°02'29.7"N +, +98°40'22.9"E +, 1335 m, 19.X.2003, H.-B. Liang & S. Yang leg. (IOZ). + + + +Distribution. + +Fig. 58 +. This species was previously known from several localities, all restricted to the southern parts of the Gaoligong Shan in western Yunnan Province, China, at elevations of 2200-2400 m ( +Kataev and Schmidt 2006 +). The new material was also collected on the southern parts of Gaoligong Shan, at elevations of 1800-2500 m, within Longling, Longyang, and Tengchong counties, western Yunnan Province, China. + + + +Habitat + +. +Specimens were collected in roadside and road cut open areas, on open, disturbed stream banks, and in other disturbed areas ( +Fig. 70 +), hidden under stones and other debris during daylight hours and active on the soil surface at night. + + + +Remarks. + +Kataev and Schmidt (2006) +indicated the absence of the parascutellar setigerous pore on elytra in + +Chydaeus convexus + +as one of the distinctive features of this species belonging to the +semenowi +group. The examination of the addition material revealed the high variability of this character. Among 125 specimens examined, the parascutellar setigerous pore was absent from only 55 specimens, in a few from only one elytron. + + + + \ No newline at end of file diff --git a/data/38/BB/DA/38BBDAE74A15541D8DC6EA64AAEB10EE.xml b/data/38/BB/DA/38BBDAE74A15541D8DC6EA64AAEB10EE.xml new file mode 100644 index 00000000000..5ec29646069 --- /dev/null +++ b/data/38/BB/DA/38BBDAE74A15541D8DC6EA64AAEB10EE.xml @@ -0,0 +1,87 @@ + + + +A nomenclator of extant and fossil taxa of the Melanopsidae (Gastropoda, Cerithioidea) + + + +Author + +Neubauer, Thomas A. +https://orcid.org/0000-0002-1398-9941 +Geological-Paleontological Department, Natural History Museum Vienna, 1010 Vienna, Austria +thomas.neubauer@nhm-wien.ac.at + +text + + +ZooKeys + + +2016 + +2016-07-05 + + +602 + + +1 +358 + + + + +http://dx.doi.org/10.3897/zookeys.602.8136 + +journal article +http://dx.doi.org/10.3897/zookeys.602.8136 +1313-2970-602-1 +65EFA27673454AC69B78DBE7E98D6103 +FFA86D39FFE2FFF3FF8AFFEBC209FFDE +126863 + + + + +† + +Melanopsis corrugata +Schuett +in +Schuett +& Ortal, 1993 + + + + + +Original +source. + + + +Schuett +and Ortal 1993 + +: 91, pl. 2, figs 15-16. + + + +Type horizon. +Pleistocene, Riss glacial epoch. + + +Type locality. + +"Galilee, southern Hula basin, about 500 m north of the new bridge over the river Jordan at Benot +Ya'Aqov" +, Israel. + + + +Types. +Paleontology Collection of the Hebrew University of Jerusalem; no number indicated. + + + \ No newline at end of file diff --git a/data/38/BC/11/38BC11C87C7B5EA941240C9CF2B754CD.xml b/data/38/BC/11/38BC11C87C7B5EA941240C9CF2B754CD.xml new file mode 100644 index 00000000000..40ac7c22600 --- /dev/null +++ b/data/38/BC/11/38BC11C87C7B5EA941240C9CF2B754CD.xml @@ -0,0 +1,88 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part D) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +474 +489 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Dolichos scarabaeoides +Linnaeus + +, + +Species Plantarum +2 + +: 726. 1753 + + +. + + + +"Habitat in India." RCN: 5341. + + + + +Lectotype +(van der Maesen in +Agric. Univ. Wageningen Pap. +85-4: 189. 1985): Herb. Hermann 1: 34, No. 282 (BM-000594465) + +. + + + + +Current name: + + +Cajanus scarabaeoides + +(L.) Thouars ex Graham + +( +Fabaceae +: +Faboideae +). + + + + \ No newline at end of file diff --git a/data/38/BC/23/38BC23428250D7AD30BC18FD803B57BE.xml b/data/38/BC/23/38BC23428250D7AD30BC18FD803B57BE.xml new file mode 100644 index 00000000000..ad87010f2a1 --- /dev/null +++ b/data/38/BC/23/38BC23428250D7AD30BC18FD803B57BE.xml @@ -0,0 +1,74 @@ + + + +Guide to the Vascular Flora of the Savannas and Flatwoods of Shaken Creek Preserve and Vicinity (Pender & Onslow Counties, North Carolina, U. S. A.) + + + +Author + +Thornhill, Robert + + + +Author + +Krings, Alexander + + + +Author + +Lindbo, David + + + +Author + +Stucky, Jon + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1099 +1099 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1099 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1099 +1314-2828--1099 + + + + +Sericocarpus linifolius (L.) Britton, Sterns & Poggenb. + + + +Distribution +Mesic pine savannas (MPS-CP), wet pine savannas (SPS-RF). + + +Notes + +Rare. +Jun-Jul +. Thornhill 1003 (NCSC). Specimens seen in the vicinity: Sandy Run [Hancock]: Taggart SARU 264 (WNC!; as S. tortifolius). [= +Aster solidagineus +Michx. sensu RAB; = FNA, Weakley] + + + + \ No newline at end of file diff --git a/data/38/BC/36/38BC3683EE8D54AB8491ADF3688B77A1.xml b/data/38/BC/36/38BC3683EE8D54AB8491ADF3688B77A1.xml new file mode 100644 index 00000000000..23ff1dce748 --- /dev/null +++ b/data/38/BC/36/38BC3683EE8D54AB8491ADF3688B77A1.xml @@ -0,0 +1,88 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part S) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +806 +877 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Silene mutabilis +Linnaeus + +, + +Centuria II Plantarum + +: 16. 1756 + + +. + + + +"Habitat in Italia." RCN: 3244. + + +Type not designated. + + + +Original material: + +Herb. Linn. No. 583.16 ( +LINN +) + +. + + + + +Current name: + + +Silene nocturna + +L. + +( +Caryophyllaceae +). + + + + \ No newline at end of file diff --git a/data/38/BC/7A/38BC7AF31E3C5723A29D6DEC897FECCB.xml b/data/38/BC/7A/38BC7AF31E3C5723A29D6DEC897FECCB.xml new file mode 100644 index 00000000000..cb00dcb9703 --- /dev/null +++ b/data/38/BC/7A/38BC7AF31E3C5723A29D6DEC897FECCB.xml @@ -0,0 +1,1146 @@ + + + +A review of Himalcercyon stat. nov., with description of a new species from the Chinese Himalaya and an updated key to Asian genera of Megasternini (Coleoptera, Hydrophilidae) + + + +Author + +Jia, Fenglong +Institute of Entomology, Life Science School, Sun Yat-sen University, Guangzhou, 510275, Guangdong, China + + + +Author + +Liang, Zulong +Institute of Entomology, Life Science School, Sun Yat-sen University, Guangzhou, 510275, Guangdong, China + + + +Author + +Fikacek, Martin +Department of Entomology, National Museum, Cirkusova 1740, CZ- 193 00 Praha 9, Czech Republic & Department of Zoology, Faculty of Science, Charles University, Vinicna 7, CZ- 128 44 Praha 2, Czech Republic +https://orcid.org/0000-0002-2078-6798 +mfikacek@gmail.com + +text + + +Deutsche Entomologische Zeitschrift + + +2020 + +67 + + +1 + + +35 +49 + + + + +http://dx.doi.org/10.3897/dez.67.50078 + +journal article +http://dx.doi.org/10.3897/dez.67.50078 +1860-1324-1-35 +56BB973DBE4E47AEBC98C1F1151C41C4 +42CBDE9B2C305189858C3A18211EA41F + + + + +Himalcercyon mirus (Hebauer, 2002) +stat. nov. +Figures 1A-D +, 2 +, 4 + + + + +Cercyon (Himalcercyon) mirus +Hebauer 2002: 39. + + + +Type locality. + +Nepal, Kathmandu district, Sheopuri Mt., 2100-2300 m a.s.l. [GPS ca +27.816672N +, +85.400000E +]. + + + +Material examined. + +Holotype +: NEPAL ● 1 ♂; Kathmandu Distr. Sheopuri Mt.; 2100-2300 m a.s.l.; 25 Jun 1988; W. Schawaller leg.; SMNS. + + +Paratypes +: NEPAL ● 2 ♀♀; same data as for holotype; SMNS ● 1 ♀; same data as for holotype; NMPC ● 1 ♀; Annapurna, Telbrung Danda; 2600-2800 m a.s.l.; 13 Jun 1997; Schmidt leg.; SMNS. + + + +Redescription. + +Form and color. +Body size 3.1-3.5 mm (3.4 mm in holotype), body width 2.0-2.1 mm (2.0 mm in holotype), widest at anterior third of elytra, weakly narrowing posteriad (Fig. +1A +). Dorsum pitchy-brown to black; head with paler clypeus; pronotal margins brown; elytral apices and posterior half of lateral elytral margins brownish; epipleuron pitchy brown laterally, reddish mesally; antenna, maxillary and labial palpi brown to reddish brown; legs reddish brown, with darker femora. + + +Head. +Clypeus with moderately dense fine setiferous semicircular punctures, smooth between punctures. Frons with punctures of the same size and density as those on clypeus, smooth between punctures. Mentum 1.4 +x +wider than long, rugose, with dense punctures (Fig. +2B +), slightly concave anteriorly. Antenna with pedicel ca 0.2 +x +as long as scape, pedicel ca. as long as antennomeres 3 and 4 combined, cupule small. + + +Thorax. +Pronotum with punctation similar to that on frons, interstices without microsculpture; lateral marginal bead shortly overlapping to anterior margin but not to posterior margin, stopping at posterior angle. Scutellar shield smooth, with five to seven punctures. Elytral striae sharply impressed (Fig. +1A +), striae 6, 8, and 9 not reaching base; intervals with finer and sparser punctures than on pronotum, each puncture bearing a fine short seta, interstices between punctures smooth. Epipleuron with bare outer and pubescent inner portion delimited from each other by a fine ridge, inner pubescent part narrower than the outer part, reaching the level of posterior part of metaventrite (Fig. +1A +). Mesoventral elevation arrowhead-shaped, ca 1.5 +x +longer than wide, sparsely pubescent (Fig. +2F +). Metaventrite with large median elevation, finely and sparsely punctate (Fig. +2E +), interstices without microsculpture; lateral portions microsculptured, with sparse coarse punctures and dense pubescence. Legs with trochanters densely pubescent, femora with sparse and moderately coarse punctures, interstice between punctures with fine microsculpture consisting of transverse lines. + + +Male genitalia. +Middle lobe of abdominal sternite IX narrow, shorter than lateral struts (Fig. +1D +). Aedeagus (Fig. +1C +) with median lobe ca as long as tegmen; paramere ca 1.5 +x +as long as phallobase. Paramere gradually narrowed from base to apex, obliquely truncate apically, widened inwards to form a process with a few setae. Median lobe ca as wide as paramere, gradually narrowing in apical third, apex narrowly rounded, gonopore subapical. + + + +Distribution. + +Known from two localities in central Nepal (Fig. +4 +). + + + + +Key to Eastern Palaearctic and Oriental genera of the +Megasternini + + +The following key is mainly based in the ventral characters, namely the form of prosternum and meso- and metaventrite, which are illustrated in Figures +5 +- +8 +. The concept of some of the genera will likely be modified in the future; the key reflects the current status. The key includes all genera occurring east of Iran, the Black Sea, and the Ural Mountains. (i.e. it does not cover the Near East and the Arabian Peninsula); eastwards it includes all regions west of New Guinea. See Table +1 +for the number of described species and references to the most important keys or taxonomic treatments for each genus. Remarks and numbers of species only refer to those from the Eastern Palaeartic and Oriental Regions. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
1 +Antennal grooves large, reaching to the lateral margin of hypomeron (Fig. +5A, B, D +). +2
- +Antennal grooves absent or small, not reaching to the lateral margin of the hypomeron (Figs +5E, F +, +6 +, +7 +, +8A-C +) +5
2 +Metaventrite with complete femoral lines reaching from posteriomesal portion to anterolateral corner (Fig. +5A, D +) +3
- +Metaventrite without complete femoral lines, at most with short vestiges anterolaterally. (Fig. +5B, C +) +4
3 +Mesoventral plate wider than long. Prosternum with wide plate without median carina (Fig. +5A +). Mentum with sharply pointed anterolateral corners (Fig. +8D +) + + +Cryptopleurum + +Mulsant +
- +Mesoventral plate approximatley as long as wide. Prosternal plate approximately as long as wide, with more or less distinct median carina (Fig. +5D +). Mentum with bluntly rounded anterolateral corners + + +Pachysternum + +Motschulsky +
4 +Median portion of prosternum roof-like, high (Fig. +5C +). Mesoventral plate longer than wide. Metaventrite without any traces of femoral lines (Fig. +5C +). Anterior tibia without anterolateral excision + + +Pacrillum + +d'Orchymont +
- +Median portion of prosternum with flat hexagonal plate, not carinate medially (Fig. +5B +). Mesoventral plate slightly wider than long. Metaventrite with vestiges of femoral lines in anterolateral corners (Fig. +5B +). Anterior tibia anterolaterally with emargination + + +Megasternum + +Mulsant +
5 +Metaventrite with postcoxal ridge widely diverging from posterior margin of coxal cavity and forming an arcuate ridge reaching lateral margin of metaventrite (Figs +5E, F +, +6A, B +) +6
- +Metaventrite with postcoxal ridge parallel to posterior margin of coxal cavity or nearly so, reaching anterolateral corner of metaventrite and not forming any arcuate ridge (Figs +6C-F +, +7 +, +8A-C +) +9
6 +Metaventrite with complete femoral lines crossing the arcuate postcoxal ridge and X-shape in form (Fig. +5E +). Mesoventral elevation narrowly elongate or narrow but widely contacting metaventrite + + +Peltocercyon + +d'Orchymont +
- +Metaventrite without X-shaped structure, femoral lines absent or short, not crossing with arcuate postcoxal ridge (Figs +5F +, +6A, B +). +7
7 +Mesoventral plate widely contacting metaventrite (Fig. +6A, B +). Median portion of prosternum at least weakly delimited from lateral portions +8
- +Mesoventral plate separated from metaventrite by a wide deep gap (Fig. +5F +). Median portion of prosternum simply carinate, not delimited from lateral portions + + +Armostus + +Sharp +
8 +Metaventrite with deep triangular impression along its lateral margin (Fig. +6A +) + + +Morastus + +d'Orchymont +
- +Metaventrite without such impression (Fig. +6B +) + + +Oosternum + +Sharp +
9 +Median portion of prosternum highly elevated and/or delimited from lateral portions by sharp ridges (Figs +6C-F +, +7A-D +) +10
- +Median portion of prosternum finely carinate, not delimited from lateral portions (Figs +7E, F +, +8A, B +) +18
10 +Pronotum with deep longitudinal grooves (Fig. +8E +). Bare portion of metaventrite very wide (Fig. +6C +). Tiny beetles: length ca 1.2 mm + + +Emmidolium + +d'Orchymont +
-Surface of pronotum without distinct longitudinal depressions. Bare portion of metaventrite confined to medial part only. Tiny to moderately large beetles11
11 +Median portion of prosternum in form of very small triangular, very highly elevated projection. Antennal grooves absent (Fig. +6D +). Abdomen with apical emargination + + +Chimaerocyon + +Fikacek +, Maruyama, +Vondracek +& Short +
-Median portion of prosternum never so tiny and not so highly elevated. Antennal grooves present, even though sometimes rather small. Abdomen never with apical emargination12
12 +Prosternal elevation with lateral margins deeply excised (Fig. +6E, F +) +13
- +Prosternal elevation with lateral margins or ridges straight (Fig. +7A-D +) +14
13 +Tiny species, 1.2-1.6 mm. Metaventrite with complete femoral lines (Fig. +6E +). Antennal grooves present + + +Paroosternum + +Scott +
- +Large species, ca 3.0 mm. Metaventrite without femoral lines (Fig. +6F +). Antennal grooves absent + + +Oreosternum + +nom. nov. +
14 +Elytral series deeply impressed with the impressions contiguous to anterior margin of each elytron (Fig. +8F, G +). Mesoventral elevation longer than wide, rhomboid to suboval (Fig. +7A, B +) +15
-Elytral series not impressed or impressions of elytral striae series not reaching anterior margin of each elytron. Mesoventral elevation elongate or as long as wide16
15 +Pronotum highly bulged in lateral view, not forming a continuous curve with elytra. Anterior margin of prosternal elevation strongly projecting anteriad (Fig. +7A +). Mesoventral elevation subrhomboid + + +Bolbonotum + +Hansen +
- +Pronotum not highly bulged in lateral view, forming a continuous curve with elytra. Anterior margin of prosternal elevation straight (Fig. +7B +). Mesoventral elevation suboval + + +Kahanga + +Hansen +
16 +Grooves for reception of procoxae ending far before the anterior margin of mesocoxal cavities (Fig. +8C +). Mesoventral plate elongate + + +Gillisius + +d'Orchymont (part)* +
- +Grooves for reception of proxocae reaching nearly the mesocoxal cavities (Fig. +7C, D +). Mesoventral elevation approximately as wide as long +17
17 +Mesoventral elevation nearly semi-elliptical (Fig. +7C +), with wide marginal rim. Postcoxal ridges on the metaventrite meeting mesally and forming a short median longitudinal ridge. Metatibiae densely pubescent ventrally (Fig. +8H +). Large species: 2.5-3.3 mm + + +Australocyon + +Hansen +
- +Mesoventral elevation more less pentagonal, without any marginal rim (Fig. +7D +). Postcoxal ridges mesally bending posteriad, remaining separate, forming two short median longitudinal ridges (in one species largely obsolete). Metatibie without dense ventral pubescence. Medium sized to tiny species: 2.0-2.9 mm + + +Nipponocercyon + +Sato +
18 +Abdominal ventrite 1 without median carina. Mesoventral elevation narrowly laminar (Fig. +7E +) + + +Cycreon + +d'Orchymont +
-Abdominal ventrite 1 carinate medially. Mesoventral elevation in form of a lamina or an elongate plate19
19 +Ventral face of meso- and metatibiae with dense, long pubescence. Ventral morphology similar to Figure +7F + + +Pilocnema + +Hansen +
- +Ventral face of meso- and metatibiae never densely pubescent, at most with sparse short setae. Ventral morphology similar to Figures +2 +, +3 +, and +8A, B +20
20 +Mesoventral elevation laminar or forming an oval elongate plate; posterior part of the plate rounded or acute (as in Fig. +8A, B +) +21
- +Mesoventral elevation elongate, but sharply cut off posteriorly, contacting metaventrite more or less in a straight line (as in Figs +2F +, +8C +) +22
21 +Median portion of prosternum with a pair of transverse ridges partly delimiting prosternal process (Fig. +8A +) + + +Pseudocercyon + +d'Orchymont +
- +Median portion of prosternum without such ridges, only simply carinate (Fig. +8B +) + + +Cercyon + +Leach +
22 +Mesoventral elevation arrowhead-shaped, with lateral angulate lobes (Figs +2F +, +3C +) + + +Himalcercyon + +Hebauer +
- +Mesoventral elevation elongate oval (as in Fig. +8C +); if small lateral lobes are present, they are below the plate +23
23India, continental Southeast Asia and China. + +Gillisius + +d'Orchymont (part) +
-Islands of the Malay Archipelago. + +Pelosoma + +Mulsant* +
+
+ + +* the type species, +G. madurensis +d'Orchymont +, 1925, keys out here. + + + + +* the status of +Gillisius +and Asian Pelosoma is unclear. + + + + +Figure 5. +Ventral view of thorax of eastern Palaearctic and Oriental genera of the +Megasternini +. +A. + +Cryptopleurum ferrugineum + +. +B. + +Megasternum concinnum + +. +C. + +Pacrillum manchuricum + +. +D. + +Pachysternum nigrovittatum + +. +E. + +Peltocercyon coomani + +. +F. + +Armostus schenklingi + +. + + + + +Table 1. +List of Eastern Palaearctic and Oriental general of the +Megasternini +, with number of described species and references to the most important keys or taxonomic treatments. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
GenusDescribed speciesKeys or original descriptions
+ +Armostus + +11 + +d'Orchymont +1942 + +; +Hebauer 2002a +; + +Hoshina and +Sato +2006 + +
+ +Australocyon + +7 +Hansen 2003 +; + +Fikacek +et al. 2012 + +
+ +Bolbonotum + +3 +Hansen 1999a +
+ +Cercyon + +148 +Shatrovskiy 1992 +; +Hansen 1999b +; +Short and Hebauer 2006 +; +Hoshina 2008 +; +Jia et al. 2011 +; +2019 +; +Ryndevich et al. 2017 +; +2019 +; +Ryndevich and Prokin 2017 +
+ +Chimaerocyon + +2 + +Fikacek +et al. 2013 + +
+ +Cryptopleurum + +7 + +d'Orchymont +1926 + +; +Jia and Zhang 2017 +
+ +Cycreon + +4 + 1 ssp. +Arriaga-Varela et al. 2018b +
+ +Emmidolium + +1 + +Fikacek +2007 + +
+ +Gillisius + +2 + +d'Orchymont +1925a + +; +1926 +
+ +Himalcercyon + +2this paper
+ +Kahanga + +1 +Hansen 1999a +
+ +Megasternum + +4 +Shatrovskiy 1989 +; + +Fikacek +et al. 2012 + +; +Ryndevich 2017 +
+ +Morastus + +1 + +d'Orchymont +; 1926 + +
+ +Nipponocercyon + +3 + +Hoshina and +Fikacek +2010 + +; + +Fikacek +et al. 2012 + +; +2015a +
+ +Oosternum + +9 +Hebauer 2002a +; + +Hoshina and +Sato +2004b + +; +2005 +
+ +Oreosternum + +1Hebauer 2002
+ +Pachysternum + +11 + +Fikacek +et al. 2012 + +
+ +Pacrillum + +5 + +Hoshina and +Sato +2004a + +; + +Fikacek +and Hebauer 2005 + +; +Shatrovskiy 1989 +as + +Agnaeformia + +
+ +Paroosternum + +5 +Hebauer 2006 +
+ +Pelosoma + +2 + +d'Orchymont +1925b + +; +1932 +
+ +Peltocercyon + +4 + +d'Orchymont +1925a + +; +Hoshina 2016 +; +2018 +
+ +Pilocnema + +1 +Hansen 2003 +
+ +Pseudocercyon + +1 + +d'Orchymont +1926 + +
+
+
+ +New replacement name + +
+
\ No newline at end of file diff --git a/data/38/BD/2A/38BD2A32A2E57D088AB269653B683301.xml b/data/38/BD/2A/38BD2A32A2E57D088AB269653B683301.xml new file mode 100644 index 00000000000..efd3d2bbc5f --- /dev/null +++ b/data/38/BD/2A/38BD2A32A2E57D088AB269653B683301.xml @@ -0,0 +1,103 @@ + + + +Order Scandentia + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +104 +109 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Anathana +Lyon 1913 + + + + + + + +Anathana +Lyon 1913 + +, + +Proc. +U. S. +Natl. Mus., 45: 120 + + +. + + + + +Type Species: + +Tupaia ellioti +Waterhouse 1850 + + + + + +Species and subspecies: +1 species: + + +Species + +Anathana ellioti +(Waterhouse 1849) + + + + + +Discussion: + +Anathana + +and + +Tupaia + +are closely allied. + + + + \ No newline at end of file diff --git a/data/38/BD/44/38BD44D27F06E1AE7301270569DFE457.xml b/data/38/BD/44/38BD44D27F06E1AE7301270569DFE457.xml new file mode 100644 index 00000000000..64698b40055 --- /dev/null +++ b/data/38/BD/44/38BD44D27F06E1AE7301270569DFE457.xml @@ -0,0 +1,76 @@ + + + +The ground beetles (Coleoptera: Carabidae) of the Strandzha Mountain and adjacent coastal territories (Bulgaria and Turkey) + + + +Author + +Kostova, Rumyana + + + +Author + +Gueorguiev, Borislav + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8135 +8135 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8135 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8135 +1314-2828--8135 + + + + +Poecilus (Poecilus) lepidus lepidus (Leske, 1785) + + + +Materials + + +Type status: +Other material +. Location: countryCode: BG; locality: +Strandzha +; Record Level: bibliographicCitation: +Gueorguiev +& +Gueorguiev +(1995: 120) + + +Type status: +Other material +. Occurrence: recordedBy: +K. Tuleshkov +; individualCount: +2 +; Location: countryCode: BG; locality: +Maslen nos Cape +; Event: eventDate: +16/07/1933 + + + + + \ No newline at end of file diff --git a/data/38/BD/5E/38BD5E5D2F2EE4CBEF4A04E7376713FB.xml b/data/38/BD/5E/38BD5E5D2F2EE4CBEF4A04E7376713FB.xml new file mode 100644 index 00000000000..5c8fd236975 --- /dev/null +++ b/data/38/BD/5E/38BD5E5D2F2EE4CBEF4A04E7376713FB.xml @@ -0,0 +1,113 @@ + + + +Annotated type catalogue of the Bulimulidae (Mollusca, Gastropoda, Orthalicoidea) in the Natural History Museum, London + + + +Author + +Breure, Abraham S. H. +Naturalis Biodiversity Center, P. O. Box 9517, Leiden, the Netherlands +bbreure@xs4all.nl + + + +Author + +Ablett, Jonathan D. +Natural History Museum, Division of Higher Invertebrates, London, SW 7 5 BD, UK + +text + + +ZooKeys + + +2014 + +2014-03-21 + + +392 + + +1 +367 + + + + +http://dx.doi.org/10.3897/zookeys.392.6328 + +journal article +http://dx.doi.org/10.3897/zookeys.392.6328 +1313-2970-392-1 +FFCF5A59FFB1FF93FFF10B43FFAFFFF5 +578044 + + + + +Bulimus schiedeanus Pfeiffer, 1841 +Figs 72D-F +, L53vi + + + + +Bulimus schiedeanus +Pfeiffer 1841 +: 43; +Reeve 1848 [1848-1850] +: pl. 54 fig. 361; +Breure 1979 +: 77. + + + +Type locality. +"Mejico (Dr. Schiede)". + + +Label. + +"Mexico" +, taxon label in +Pfeiffer's +handwriting. M.C. label style IV. + + + +Dimensions. +"Long. 16, diam. 9 lin. [H 34.8, D 19.6 mm]"; figured specimen herein H 28.4, D 16.0, W 6.2. + + +Type material. +NHMUK 1975240, three probable syntypes (Cuming coll.). + + +Remarks. + +Pfeiffer probably described this taxon from a specimen in his own collection, which is likely to be lost. The measurements given by Pfeiffer are thus interpreted as German lines. The specimens from +Cuming's +collection also bear +Pfeiffer's +handwriting and are probably the only extant ones that confirms his identification; they are considered as probable syntypes. The current systematic position follows +Thompson (2011 +: 127). + + + +Current systematic position. + +Bulimulidae +, + +Rabdotus (Rabdotus) schiedeanus schiedeanus + +(Pfeiffer, 1841). + + + + \ No newline at end of file diff --git a/data/38/BD/60/38BD6059532A6671CB93DB9E0E3C51D9.xml b/data/38/BD/60/38BD6059532A6671CB93DB9E0E3C51D9.xml new file mode 100644 index 00000000000..84c52179105 --- /dev/null +++ b/data/38/BD/60/38BD6059532A6671CB93DB9E0E3C51D9.xml @@ -0,0 +1,314 @@ + + + +Info Flora Schweiz - Asteraceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/asteraceae.html + +url + + + + + +Leucanthemum adustum +(W. D. J. Koch) Gremli subsp. +adustum + + + + + +Unterart ISFS: 236250 Checklist: 1026655 +Asteraceae +Leucanthemum +Leucanthemum vulgare +aggr. +Leucanthemum adustum (W. D. J. Koch) Gremli +Leucanthemum adustum (W. D. J. Koch) Gremli subsp. adustum + + + +Bestimmungsschluessel + + + +Zusammenfassung +KEINE ANGABE + + + +Status Nationale +Prioritaet + +: -- + + +Internationale Verantwortung +: -- + + + +Oekologie + + + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + + + + + +
KEINE ANGABE
+
+
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F--Lichtzahl L--Salzzeichen--
Reaktionszahl R--Temperaturzahl T--
+Naehrstoffzahl +N +-- +Kontinentalitaetszahl +K +--
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Leucanthemum adustum +(W. D. J. Koch) Gremli subsp. +adustum + + + + + +Volksname + + + +Deutscher Name: -- Nom +francais +: -- Nome italiano: -- + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Leucanthemum adustum (W. D. J. Koch) Gremli subsp. adustum + + +Checklist 2017 + +236250
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Kommentare aus der +Checklist 2017 +Neue Unterart: Die Art wurde bisher (SISF-2) nicht in Unterarten aufgeteilt oder die Unterteilung wurde bisher nicht akzeptiert. Im Gebiet der +Checklist 2017 +kommt nur diese Unterart vor. Sie ist der Unterart + +L. a. +subsp. +margaritae +( +Gayer +) Holub + +aus den Ostalpen und Karpaten +gegenuebergestellt +. Die Zuordnung zur Unterart sollte nur erfolgen, wenn ihre Bestimmung als solche sichergestellt ist. Checklist + + + + +Status Indigenat +: Indigen + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein Status Rote Liste national + + + + + + +
KEINE ANGABE
+
+ + +Status nationale +Prioritaet +/Verantwortung + + + + + + + + + + + + + + + + + + + + + + +
+ +Nationale +Prioritaet + +--
+Massnahmenbedarf +--
+ +Internationale Verantwortung + +--
+ +Ueberwachung +Bestaende + +--
+
+ +Schutzstatus + + + + + + +
Kein internationaler, nationaler oder kantonaler Schutz
+
+
+
+
\ No newline at end of file diff --git a/data/38/BD/82/38BD82950711B2BEC75EA17EEDE92CB1.xml b/data/38/BD/82/38BD82950711B2BEC75EA17EEDE92CB1.xml new file mode 100644 index 00000000000..284a7bbdf98 --- /dev/null +++ b/data/38/BD/82/38BD82950711B2BEC75EA17EEDE92CB1.xml @@ -0,0 +1,272 @@ + + + +Saproxylic beetles of the Po plain woodlands, Italy + + + +Author + +Stefanelli, Silvia + + + +Author + +Della Rocca, Francesca + + + +Author + +Bogliani, Giuseppe + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1106 +1106 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1106 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1106 +1314-2828--1106 + + + + +Enicmus rugosus (Herbst, 1793) + + + + +Lathridius ferrugineus +Gerhardt, 1912 - +Fauna Europaea (2013) + + +Enicmus frater +Weise, 1972 - +Fauna Europaea (2013) + + +Lathridius ruficornis +Kugelann, 1794 - +Fauna Europaea (2013) + + +Lathridius rugipennis +Mannerheim, 1844 - +Fauna Europaea (2013) + + +Lathridius depressus +Grimmer, 1841 - +Fauna Europaea (2013) + + +Lathridius planatus +Mannerheim, 1844 - +Fauna Europaea (2013) + + + +Materials + + +Type status: +Other material +. Occurrence: recordedBy: +Silvia Stefanelli +; individualCount: +67 +; lifeStage: +adult +; Taxon: taxonID: urn:lsid:faunaeur.org:taxname:398120; scientificName: Enicmusrugosus; order: Coleoptera; family: Latridiidae; genus: Enicmus; scientificNameAuthorship: Herbst 1793; Location: country: +Italy +; stateProvince: Pavia; locality: +SIC "Boschi Siro Negri e Moriano" - BN1 +; verbatimElevation: +68 m +; verbatimCoordinates: 32T 503258E 5007870N; verbatimCoordinateSystem: UTM WGS 84; decimalLatitude: +45.224312 +; decimalLongitude: +9.041499 +; georeferencedBy: Silvia Stefanelli; georeferenceProtocol: GPS; Identification: identifiedBy: + +Wolfgang +Ruecker + +; dateIdentified: 2011 + + +Type status: +Other material +. Occurrence: recordedBy: +Silvia Stefanelli +; individualCount: +57 +; lifeStage: +adult +; Taxon: taxonID: urn:lsid:faunaeur.org:taxname:398120; scientificName: Enicmusrugosus; order: Coleoptera; family: Latridiidae; genus: Enicmus; scientificNameAuthorship: Herbst 1793; Location: country: +Italy +; stateProvince: Pavia; locality: +SIC "Boschi Siro Negri e Moriano" - BN21 +; verbatimElevation: +66 m +; verbatimCoordinates: 32T 506342E 5005026N; verbatimCoordinateSystem: UTM WGS 84; decimalLatitude: +45.198691 +; decimalLongitude: +9.080746 +; georeferencedBy: Silvia Stefanelli; georeferenceProtocol: GPS; Identification: identifiedBy: + +Wolfgang +Ruecker + +; dateIdentified: 2011 + + +Type status: +Other material +. Occurrence: recordedBy: +Silvia Stefanelli +; individualCount: +524 +; lifeStage: +adult +; Taxon: taxonID: urn:lsid:faunaeur.org:taxname:398120; scientificName: Enicmusrugosus; order: Coleoptera; family: Latridiidae; genus: Enicmus; scientificNameAuthorship: Herbst 1793; Location: country: +Italy +; stateProvince: Pavia; locality: +SIC "Boschi Siro Negri e Moriano" - BN5 +; verbatimElevation: +62 m +; verbatimCoordinates: 32T 502886E 5008393N; verbatimCoordinateSystem: UTM WGS 84; decimalLatitude: +45.229029 +; decimalLongitude: +9.036770 +; georeferencedBy: Silvia Stefanelli; georeferenceProtocol: GPS; Identification: identifiedBy: + +Wolfgang +Ruecker + +; dateIdentified: 2011 + + +Type status: +Other material +. Occurrence: recordedBy: +Silvia Stefanelli +; individualCount: +60 +; lifeStage: +adult +; Taxon: taxonID: urn:lsid:faunaeur.org:taxname:398120; scientificName: Enicmusrugosus; order: Coleoptera; family: Latridiidae; genus: Enicmus; scientificNameAuthorship: Herbst 1793; Location: country: +Italy +; stateProvince: Pavia; locality: +SIC "Boschi Siro Negri e Moriano" - BN10 +; verbatimElevation: +76 m +; verbatimCoordinates: 32T 504479E 5006332N; verbatimCoordinateSystem: UTM WGS 84; decimalLatitude: +45.210461 +; decimalLongitude: +9.057038 +; georeferencedBy: Silvia Stefanelli; georeferenceProtocol: GPS; Identification: identifiedBy: + +Wolfgang +Ruecker + +; dateIdentified: 2011 + + +Type status: +Other material +. Occurrence: recordedBy: +Silvia Stefanelli +; individualCount: +43 +; lifeStage: +adult +; Taxon: taxonID: urn:lsid:faunaeur.org:taxname:398120; scientificName: Enicmusrugosus; order: Coleoptera; family: Latridiidae; genus: Enicmus; scientificNameAuthorship: Herbst 1793; Location: country: +Italy +; stateProvince: Pavia; locality: +SIC "Boschi di Vaccarizza" - V1 +; verbatimElevation: +62 m +; verbatimCoordinates: 32T 519272E 4999526N; verbatimCoordinateSystem: UTM WGS 84; decimalLatitude: +45.148947 +; decimalLongitude: +9.245157 +; georeferencedBy: Silvia Stefanelli; georeferenceProtocol: GPS; Identification: identifiedBy: + +Wolfgang +Ruecker + +; dateIdentified: 2011 + + +Type status: +Other material +. Occurrence: recordedBy: +Silvia Stefanelli +; individualCount: +57 +; lifeStage: +adult +; Taxon: taxonID: urn:lsid:faunaeur.org:taxname:398120; scientificName: Enicmusrugosus; order: Coleoptera; family: Latridiidae; genus: Enicmus; scientificNameAuthorship: Herbst 1793; Location: country: +Italy +; stateProvince: Pavia; locality: +SIC "Boschi di Vaccarizza" - V2 +; verbatimElevation: +65 m +; verbatimCoordinates: 32T 519868E 4999488N; verbatimCoordinateSystem: UTM WGS 84; decimalLatitude: +45.148589 +; decimalLongitude: +9.252737 +; georeferencedBy: Silvia Stefanelli; georeferenceProtocol: GPS; Identification: identifiedBy: + +Wolfgang +Ruecker + +; dateIdentified: 2011 + + + + +Distribution + +Austria, Belarus, Belgium, Bosnia and Herzegovina, Britain I., Bulgaria, Croatia, Czech Republic, Danish mainland, Estonia, Finland, French mainland, Germany, Greek mainland, Hungary, Italian mainland, Latvia, Lithuania, Norwegian mainland, Poland, Portuguese mainland, Romania, Russia Central, Russia East, Russia North, Russia Northwest, Slovakia, Slovenia, Spanish mainland, Switzerland, The Netherlands, Ukraine, Yugoslavia, East Palaearctic, North Africa ( +Fauna Europaea 2013 +). + + + +Notes + +The species lives under the bark of old forest deadwood, mainly in oak but also in ash, beech, alder, and pine trees. It usually lives associated with fungi of the genus +Lycoperdacea +, +Polyporacea +, and myxomycetes ( +Alexander 2002 +, + +Ruecker +2004 + +). + + + + \ No newline at end of file diff --git a/data/38/BD/AF/38BDAF7F870B595D996D24C2D0ADB186.xml b/data/38/BD/AF/38BDAF7F870B595D996D24C2D0ADB186.xml new file mode 100644 index 00000000000..a7940ed0ce4 --- /dev/null +++ b/data/38/BD/AF/38BDAF7F870B595D996D24C2D0ADB186.xml @@ -0,0 +1,118 @@ + + + +Nomenclatural changes in Coleus and Plectranthus (Lamiaceae): a tale of more than two genera + + + +Author + +Paton, Alan J. + + + +Author + +Mwanyambo, Montfort + + + +Author + +Govaerts, Rafael H. A. + + + +Author + +Smitha, Kokkaraniyil + + + +Author + +Suddee, Somran + + + +Author + +Phillipson, Peter B. + + + +Author + +Wilson, Trevor C. + + + +Author + +Forster, Paul I. + + + +Author + +Culham, Alastair + +text + + +PhytoKeys + + +2019 + +129 + + +1 +158 + + + + +http://dx.doi.org/10.3897/phytokeys.129.34988 + +journal article +http://dx.doi.org/10.3897/phytokeys.129.34988 +1314-2003-129-1 +BF57C6B3C3065AEE9B4B3D47189C908F +3382366 + + + + + +Coleus otostegioides ( +Guerke +) A.J.Paton + +comb. nov. + + + + +Capitanya otostegioides +Guerke +, Bot. Jahrb. Syst. 21: 106. 1895. + + +Plectranthus otostegioides +( +Guerke +) Ryding, Kew Bull. 54: 126. 1999. Types: Eritrea, upper Lebka valley, Heuglin s.n. (syntype: B, destroyed) & +Mueller-Prosko-Capitany +s.n. (syntype: B, destroyed) & Tanzania, Kilimanjaro, Volkens 492 (syntype: B, destroyed); neotype: Tanzania, Arusha District: Ngaserai Plain, Richards & Arasululu 26472 (neotype: K, designated by +Ryding (1999) +). + + + +Distribution. +NE. Trop. Africa to N. Tanzania. + + + \ No newline at end of file diff --git a/data/38/BE/41/38BE410D2B66CD4AC5F91D53B22905DC.xml b/data/38/BE/41/38BE410D2B66CD4AC5F91D53B22905DC.xml new file mode 100644 index 00000000000..7d3c3bfd439 --- /dev/null +++ b/data/38/BE/41/38BE410D2B66CD4AC5F91D53B22905DC.xml @@ -0,0 +1,123 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part S) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +806 +877 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Schmidelia racemosa +Linnaeus + +, + +Systema Naturae +, ed. 12, 2 + +: 274; + +Mantissa Plantarum + +: 67. 1767 + + +. + + + + +"Habitat in +India +orientali sub Klinting birae." RCN: 2848. + + + + +Neotype +(Adema in Jarvis & al., +Regnum Veg. +127: 86. 1993): +Kleynhoff +sheet No. 908.269-889 (L). + + + + +Generitype +of + +Schmidelia +Linnaeus + +, +nom. illeg. +, non Boehm. + + + + +Current name: + + +Allophylus cobbe + +(L.) Raeusch. + +( +Sapindaceae +). + + + + + +Note: + +Schmidelia +Linnaeus (1767) + + +is a later homonym of + +Schmidelia +Boehm. (1760) + +and therefore illegitimate. + + + + \ No newline at end of file diff --git a/data/38/BF/82/38BF82DD132754EEBFAE7167A564531B.xml b/data/38/BF/82/38BF82DD132754EEBFAE7167A564531B.xml new file mode 100644 index 00000000000..b57e0990b93 --- /dev/null +++ b/data/38/BF/82/38BF82DD132754EEBFAE7167A564531B.xml @@ -0,0 +1,329 @@ + + + +On Chinese Trachyphloeini with description of four new species (Coleoptera, Curculionidae, Entiminae) + + + +Author + +Ren, Li +Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, No. 1 Beichen West Road, Chaoyang District, Beijing 100101, China +https://orcid.org/0000-0002-8597-0449 + + + +Author + +Borovec, Roman +Czech University of Life Sciences Prague, Faculty of Forestry and Wood Sciences, Department of Forest Protection and Entomology, Kamycka 1176, CZ- 165 21 Praha 6 - Suchdol, Czech Republic + + + +Author + +Zhang, Runzhi +Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, No. 1 Beichen West Road, Chaoyang District, Beijing 100101, China & University of Chinese Academy of Sciences, Beijing 100049, China +https://orcid.org/0000-0001-9001-0154 +zhangrz@ioz.ac.cn + +text + + +ZooKeys + + +2020 + +974 + + +93 +119 + + + + +http://dx.doi.org/10.3897/zookeys.974.56059 + +journal article +http://dx.doi.org/10.3897/zookeys.974.56059 +1313-2970-974-93 +A7F28C32A0644CAB8F6674462E6D54A4 +3C4B40D4246C57A680AA7657C27AD210 + + + + +Trachyphloeosoma jirka +sp. nov. +Figs 21 +, 22 +, 37 +, 41 +, 45 +, 49 +, 54 + + + +Type locality. +China, Jiangxi, Jinggangshan Mts., Xiangzhou. + + +Material examined. + +Holotype. +China - +Jiangxi Prov. +• 1 ♀; Jinggangshan Mts., Xiangzhou (forested valley S of the village); +26°35.5'N +, +114°16.0'E +; 374 m a.s.l.; 26 Apr. 2011; +Fikacek +& +Hajek +leg.; sifting, accumulation of moist leaf litter along the stream and on the steep slope above the stream in the sparse secondary forest; [MF08]; NMPC. +Paratypes. +China - +Jiangxi Prov. +• 1 ♀; the same data as holotype; NMPC; • 1 ♀; same data as holotype; IZCAS. + + + +Description. +Body length: 2.06-2.44 mm, holotype 2.06 mm. + +Body +(Figs +21 +, +22 +) including antennae and legs unicoloured piceous brown. The entire body except for frons, antennal funicles with clubs and tarsi covered with a brownish earth-like incrustation which conceals most of the surface; appressed scales, covering the whole body, with hardly visible shape, but in lateral parts rounded, finely densely striolate. Elytra with one conspicuous, dense row of long erect setae on each interval, starting from the base; setae as long as width of one interval, very slender, slightly and evenly enlarged apicad, distance between two setae slightly longer than length of one seta. Pronotum and head with rostrum with identically long and shaped setae as elytral setae, densely irregularly scattered, anteriorly directed. Antennal scapes, femora and tibiae with long, erect, very slender setae, distinctly prominent from outline of scapes and legs. + + +Rostrum +(Figs +21 +, +22 +, +37 +) 1.12-1.18 +x +wider than long, at base 1.18-1.20 +x +wider than at apex, evenly tapered anteriad, at basal half with straight sides; in profile moderately long and slender, convex, at apex distinctly declined. Epifrons in basal half distinctly tapered anteriad, in apical half almost parallel-sided, narrow, 0.61-0.67 +x +as wide as rostrum in corresponding part, with ill-defined, slender, longitudinal furrow. Frons conspicuous, smooth, shiny, angularly declined from epifrons. Epistome small, short, indistinct, just at apical portion of rostrum, posteriorly narrowly carinate. Antennal scrobes in dorsal view visible as wide furrows, reaching eyes; in lateral view distinctly subtriangular, strikingly enlarged posteriad with dorsal margin directed above dorsal margin of eye and ventral margin deeply below ventral margin of eye. Eyes small, in dorsal view hardly protruding from outline of head; in lateral view placed subdorsally, distance from dorsal margin of head shorter than diameter of eye. + + +Antennae +moderately long, scapes slightly exceeding anterior margin of pronotum and distinctly longer than funicle, weakly curved in basal third, in apical half slightly gradually thickened to apex, at apex 0.7-0.8 +x +as wide as club. Funicle segment 1 bead-shaped, 1.3-1.4 +x +longer than wide and 1.4-1.5 +x +longer than segment 2, this is short, 1.1-1.2 +x +longer than wide; segments 3-7 slightly successively wider, segment 3 and 4 1.3-1.4 +x +, segment 5-6 1.5-1.6 +x +, segment 7 1.7-1.8 +x +wider than long. Clubs ovoid, large, 1.6-1.7 +x +longer than wide. + + +Pronotum +(Figs +21 +, +22 +) 1.21-1.28 +x +wider than long, widest at anterior third, with distinctly rounded sides, slightly constricted behind anterior margin; disc flatly and irregularly granulate, among granules irregularly punctate with rough and fine punctures; in lateral view pronotum slightly convex, anterior margin strongly obliquely directed back beneath towards coxae. + + +Elytra +(Figs +21 +, +22 +) oval, 1.42-1.46 +x +longer than wide, widest at midlength, with regularly rounded sides. Striae coarsely punctate, twice as wide as intervals, striae not impressed between the punctures; separations of punctures much less than their diameters. Intervals very narrow, flat, shiny. + + +Protibiae +(Fig. +41 +) long and slender, 6.1-6.3 +x +longer than wide at midlength, at apical quarter conspicuously curved inwards with mesal edge slightly bisinuate, apically obliquely subtruncate, with dense fringe of fine but long yellowish setae, shorter in mesal than in lateral part, with long and slender yellowish mucro. Tarsi short, tarsomere 2 1.4-1.5 +x +wider than long; tarsomere 3 1.3-1.4 +x +wider than long and 1.4-1.5 +x +wider than tarsomere 2; tarsomere 5 1.1 +x +as long as tarsomere 3, evenly widened apicad with very long, strongly divaricate claws, approximately as long as part of onychium (tarsomere 5) projecting beyond lobes of tarsomere 3. + + +Abdominal ventrites +sparsely roughly punctate; ventrite 2 slightly longer than ventrite 1 and distinctly longer than ventrites 3 and 4 combined; suture between ventrites 1 and 2 sinuate, the others straight. Metaventral process as wide as transverse diameter of metacoxa. + + +Female genitalia. +Spermatheca with very slender and irregularly distorted cornu; corpus large, elongate; ramus not developed; collum very small, hump-shaped, shorter than wide (Fig. +45 +). Sternite VIII with plate 2.0-2.2 +x +longer than wide, rhombic, without any fenestra (Fig. +49 +). Gonocoxites of ovipositor very slender and long, basally enlarged, in apical part rod-shaped, bearing slender and long cylindrical stylus with apical setae. + + + +Figures 36-41. +Head with rostrum in dorsal and lateral view of + +Trachyphloeosoma + +species: +36 + +T. honza + +sp. nov. +37 + +T. jirka + +sp. nov. +38 + +T. martin + +sp. nov. +39 + +T. roelofsi + +; Protibiae of + +Trachyphloeosoma + +species: +40 + +T. honza + +sp. nov. +41 + +T. jirka + +sp. nov. Scale bars: 0.50 mm ( +36-41 +). + + + + +Bionomics. +This species was collected by sifting in sparse secondary forest. + + +Etymology. + +This species is dedicated to Dr. +Jiri +Hajek +, curator of National Museum in Prague, who loaned us very interesting material of + +Trachyphloeosoma + +for study and also collected the specimens of this species. The nickname of +Jiri +is +"Jirka" +in the Czech language. The specific name is a noun in apposition. + + + +Distribution. + +China, Jiangxi (Fig. +54 +). + + + +Differential diagnosis. + + +Trachyphloeosoma jirka + +sp. nov. is easily distinguishable among Chinese + +Trachyphloeosoma + +species by its long and slender protibiae, distinctly curved inwards at apical part, long piliform setae as long on pronotum as on elytra, long and slender rostrum with frons distinctly declined downwards, subdorsal eyes and long and slender plate of female sternite VIII. In comparison with non-Chinese species, + +T. jirka + +sp. nov. is, in the funicle 7-segmented, body covered by appressed setae and elytra with raised setae on all intervals similar to + +T. advena + +Zimmerman, 1956, known from Japan, Korea and introduced to U.S.A. and + +T. ryukyuensis + +Morimoto, 2015, known from Japan. It is possible to distinguish it from both by erect setae on pronotum equal in length to elytral setae (distinctly shorter in + +T. advena + +and + +T. ryukyuensis + +), elytra long, oval, 1.42-1.46 +x +longer than wide (oval, 1.26-1.31 +x +longer than wide long in + +T. advena + +and + +T. ryukyuensis + +) and protibiae slender, distinctly curved inwards at apical portion (short and robust, only slightly curved in + +T. advena + +and + +T. ryukyuensis + +) and also plate of sternite VIII in females without fenestra (with fenestra in + +T. advena + +and + +T. ryukyuensis + +). + + + + \ No newline at end of file diff --git a/data/38/BF/AC/38BFAC5DF1D055418F0084FBD1F32B40.xml b/data/38/BF/AC/38BFAC5DF1D055418F0084FBD1F32B40.xml new file mode 100644 index 00000000000..42e3661cd97 --- /dev/null +++ b/data/38/BF/AC/38BFAC5DF1D055418F0084FBD1F32B40.xml @@ -0,0 +1,283 @@ + + + +A systematic review of the Neotropical social wasp genus Angiopolybia Araujo, 1946 (Hymenoptera: Vespidae): species delimitation, morphological diagnosis, and geographical distribution + + + +Author + +Barroso, Paulo Cezar Salgado +https://orcid.org/0000-0002-0358-5142 +Programa de Pos-Graducao em Ciencias Biologicas (Entomologia), Coordenacao de Biodiversidade, Instituto Nacional de Pesquisas da Amazonia (INPA), Av. Andre Araujo, 2.936, Petropolis, 69067 - 375, Manaus, Brazil +pc.salgadobarroso@gmail.com + + + +Author + +Menezes, Rodolpho Santos Telles +https://orcid.org/0000-0002-6612-3543 +Programa de Pos-Graduacao em Biodiversidade Animal, Centro de Ciencias Naturais e Exatas, Universidade Federal de Santa Maria (UFSM), Av. Roraima, 1000, Camobi, 97105 - 900, Santa Maria, Brazil & Laborato ́ rio de Biologia Comparada e Abelhas, Departamento de Biologia, Faculdade de Filosofia, Cie ̂ ncias e Letras (FFCLRP), Universidade de Sa ̃ o Paulo (USP), Av. Bandeirantes, 3900, Monte Alegre, 14040 - 901, Ribeira ̃ o Preto, SP, Brazil +rstmenezes@gmail.com + + + +Author + +de Oliveira, Marcio Luiz +Programa de Pos-Graducao em Ciencias Biologicas (Entomologia), Coordenacao de Biodiversidade, Instituto Nacional de Pesquisas da Amazonia (INPA), Av. Andre Araujo, 2.936, Petropolis, 69067 - 375, Manaus, Brazil + + + +Author + +Somavilla, Alexandre +Programa de Pos-Graducao em Ciencias Biologicas (Entomologia), Coordenacao de Biodiversidade, Instituto Nacional de Pesquisas da Amazonia (INPA), Av. Andre Araujo, 2.936, Petropolis, 69067 - 375, Manaus, Brazil + +text + + +Arthropod Systematics & amp; Phylogeny + + +2022 + +2022-03-02 + + +80 + + +75 +97 + + + + +http://dx.doi.org/10.3897/asp.80.e71492 + +journal article +http://dx.doi.org/10.3897/asp.80.e71492 +1864-8312-80-75 +F85F11D5313D4A75B3907FDCCCA9376F +372E1AF5D7675176AD2805DFE2F0E6DA + + + + +Angiopolybia zischkai Richards, 1978 + + + + +Figs 3a-d +, 7h + + + + +Angiopolybia zischkai +Richards, 1978: 30 (list of mimicry), 231 (key, fig. 94), 234 (description); +Andena et al., 2007 +: 59 (phylogenetic discussion), 60 (table 2 - character matrix), 62 (fig. 3A, 5 - cladogram), 63 (key), 64 (locality of examined specimens) [examined by images]. + + + +Type locality. +Zumbi, Ecuador. + + +Diagnosis. +Anterior wing of 8-9.5 mm; eyes with medium-sized and sparse bristles; rounded gena; pronotal lamella low on the anterior margin, one fifth of the height of antennal socket; pronotal lobe not developed in the lateral anterior region, below of the pronotal fovea; defined pronotal fovea, but little deep; axillary fossa with anterior margin directed to the posterior region; posterior submedian translucent mark of the propodeum inserted in a round depression; metapleural basalar area with divergent upper and lower margins. + + +Redescription of female (Fig. 3a-c). + +Size. +(1) Head 1.03 mm long, 2.09 mm high, and 2.24 mm wide; (2) mesosoma 3.54 mm long, anterior wing 9.42 mm long, and posterior wing 6.10 mm long; (3) metasoma 5.9 mm long. +Head. +(1) Lateral ocelli with 0.16 mm and median ocellus with 0.18 mm of diameter, not inserted in a declivity of the vertex and the lateral ocelli separated from the eyes for twice its diameter. (2) Compound eyes with medium-sized and sparse bristles. (3) Frons with interantennal space with 1.75 times the height of antennal socket. Anterior tentorial fovea closer to the antennal socket than to the eye. Central region of the frons with long bristles. (4) Antennal socket 0.24 mm high. (5) Clypeus 0.9 times higher than wide, contact with eyes for a distance greater than twice the height of antennal socket, and lateral lobe touching the eye. Long bristles all over the clypeus and very long bristles on the apical margin. (6) Gena with half of the width of the eye at the level of the ocular sinus. +Mesosoma. +(1) Anterior lamella of pronotum with height of one fifth of the height of antennal socket. Pronotal fovea with ellipsoid shape, little deep and with slight anterior prominence. (2) Mesoscutum subconvex and as long as wide. (3) Tegula 1.5 times longer than wide. (4) Axillary fossa with anterior margin directing to the posterior region. (5) Propodeum with translucent posterior submedian mark, anterior to the propodeal valve, inserted in a round depression. Propodeal valve complete and expanded, median region with two thirds of the height of antennal socket. (6) Anterior wing with prestigma as long as wide. (7) Posterior wing with eight hamuli. +Metasoma +: (1) Metasomal tergum I 2.1 times longer than wide. Tergum with angulation in the posterior third, in lateral view. (2) Metasomal tergum II 0,82 times longer than broad. +Color. +Dark brown in general. Yellow: lateral of the vertex, lateral of the frons, clypeus (but dark brown disc), interantennal region, mandibles, malar space, gena, slender band contouring the posterior margin of the pronotum, outer margins of the tegula, wide spot at along the anterior margin of the scrobal furrow and along the dorsal groove of the mesoepisternum, anterior half of the metanotum, submedian longitudinal band on the propodeum, lateral margin of the propodeum, upper region of the metapleural basalar area. Yellowish brown: FL7-10 of the antenna, anterior and median coxae, trochanters, femora, tibiae and tarsi (but with dorsal brown spots). Black: ocellar area, FL1-6 of the antenna, mesoscutum and metasoma. Wings with hyaline cells, except yellow in the costal, medial, submarginal I and marginal; and yellowish-brown venation, except brown in the veins C, Sc+R, M+Cu, M and in the beginning of the Cu. + + + +Figure 3. +Holotype, female of + +Angiopolybia zischkai + +Richards, 1978: +a. +lateral view, +b. +head in frontal view, +c. +dorsal view, +d. +labels of type specimen. Scale: 1 mm. Source: Steve Thurston, AMNH. + + + + +Male. +Unknown. + + +Morphological variation (Fig. 7h). +We found a specimen with yellow color and black marks, and the abdomen, apparently, wider in dorsal view. + + +Nest. + +Not described, but +Valverde et al. (2019) +in the identification key of social wasps from Costa Rica commented that the nest envelope resembles an inverted flask. + + + +Comparative comments. + + +Angiopolybia zischkai + +resembles + +A. pallens + +, but it is distinguished by the pronotum without a developed lobe in the lateroanterior region, which is present in + +A. pallens + +; metapleural basalar area with divergent upper and lower margins, which are parallel in + +A. pallens + +; and pronotal fovea with translucent mark of elliptical shape, which is circular in + +A. pallens + +. + + + +Additional comments. + +One specimen designated as holotype of + +Angiopolybia brunnescens + +(Fig. +7h +) but not described by Richards (specimen deposited in the NHM) is an + +A. zischkai + +specimen with more yellowish coloration, similar to the color of some + +A. pallens + +. The two specimens with the labels: Paratype / PERU: 1.609, Maracapata [Marcapata] ( +Peru +) / + +Stelopolybia infernalis + +Ducke rev.11. [1911] (1 ♂, MZUSP), and 1.609, Maracapata [Marcapata] ( +Peru +) / + +Stelopolybia infernalis + +Ducke rev.11. [1911] / +A. pallens (Lep.) f. zischkai +, Rich. 4 ♀ (1 ♀, MZUSP), that are two of the paratypes of + +A. zischkai + +, are specimens of + +A. pallens + +with coloration resemble to the holotype of + +A. zischkai + +. Although +Gomes et al. (2018 +, +2020 +) reported + +A. zischkai + +samples from the Brazilian states +Rondonia +and Acre, we did not find + +A. zischkai + +for these regions. + + + +Holotype. + +♀, Holotype / Zumbi, Rio Zamora, 700M, Ecuador / XI.2.41, D.B.Laddey / + +Angiopolybia pallens + +ssp., + +Angiopolybia zischkai + +Rich., ♀ Holotype / AMNH_IZC 00332335 (AMNH, New York) (Fig. +3 +). Type specimen analyzed by images. + + + +Type material examined. + +Paratype: Paratype / PERU: Dept. Huanuco, Divisoria, 7.viii.1949, J.M.Schuncke., B.M.1952-645 / + +Angiopolybia zischkai + +Rich., ♀, paratype (1 ♀, NHM). + + + +Additional material examined. + +We examined +three females +of + +A. zischkai + +; see supplementary material S1. + + + +Geographic distribution. + +Bolivia: Cochabamba; Colombia: Amazonas, Cundinamarca, Magdalena, Putumayo, Valle del Cauca ( +new record +); Costa Rica: Heredia; Ecuador: Orellhana, Zamora-Chinchipe; Panama: +Colon +; Peru: Cuzco, +Huanuco +, +Junin +, Loreto, Pasco, Ucayali (Fig. +10b +). + + + + \ No newline at end of file diff --git a/data/38/C0/31/38C0314FA3EC0E9FE0C2E20C72E3200A.xml b/data/38/C0/31/38C0314FA3EC0E9FE0C2E20C72E3200A.xml new file mode 100644 index 00000000000..c4423844a38 --- /dev/null +++ b/data/38/C0/31/38C0314FA3EC0E9FE0C2E20C72E3200A.xml @@ -0,0 +1,90 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part U) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +906 +910 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Urtica capitata +Linnaeus + +, + +Species Plantarum +2 + +: 985. 1753 + + +. + + + +"Habitat in Canada. Kalm." RCN: 7140. + + + + +Lectotype +(Wilmot-Dear & Friis in +Opera Bot. +129: 18. 1996): +Kalm +, Herb. Linn. No. 1111.15, lower right specimen ( +LINN +) + +. + + + + +Current name: + + +Boehmeria cylindrica + +(L.) Sw. + +( +Urticaceae +). + + + + \ No newline at end of file diff --git a/data/38/C0/42/38C0428B73033B3A9BE14194CE987651.xml b/data/38/C0/42/38C0428B73033B3A9BE14194CE987651.xml new file mode 100644 index 00000000000..8348c3b9da5 --- /dev/null +++ b/data/38/C0/42/38C0428B73033B3A9BE14194CE987651.xml @@ -0,0 +1,63 @@ + + + +Checklist of British and Irish Hymenoptera - aculeates (Apoidea, Chrysidoidea and Vespoidea) + + + +Author + +Else, George R. + + + +Author + +Bolton, Barry + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8050 +8050 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8050 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8050 +1314-2828-4-8050 + + + + +Hypoponera Santschi, 1938 + + + +Notes + +Hypoponera gibbinota +(Forel, 1912, +Ponera +) was described from a worker casually introduced to Britain. + + + + \ No newline at end of file diff --git a/data/38/C0/A3/38C0A3007E6FF940EC61A941CDCF6FFD.xml b/data/38/C0/A3/38C0A3007E6FF940EC61A941CDCF6FFD.xml new file mode 100644 index 00000000000..9d5ee6550bb --- /dev/null +++ b/data/38/C0/A3/38C0A3007E6FF940EC61A941CDCF6FFD.xml @@ -0,0 +1,73 @@ + + + +Order Chiroptera - Family Phyllostomidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +395 +426 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Phyllonycteris (Phyllonycteris) +Gundlach 1860 + + + + + + + +Phyllonycteris (Phyllonycteris) +Gundlach 1860 + +, +Monatsb. K. Preuss. Akad. Wiss. Berlin, 1860: 817 + +. + + + + +Type Species: + +Phyllonycteris (Phyllonycteris) poeyi +Gundlach 1861 + + + + + \ No newline at end of file diff --git a/data/38/C1/3D/38C13D89D329B0CA6929357FA46F7FFC.xml b/data/38/C1/3D/38C13D89D329B0CA6929357FA46F7FFC.xml new file mode 100644 index 00000000000..86c595a63ae --- /dev/null +++ b/data/38/C1/3D/38C13D89D329B0CA6929357FA46F7FFC.xml @@ -0,0 +1,80 @@ + + + +Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea + + + +Author + +Dale-Skey, Natalie + + + +Author + +Askew, Richard R. + + + +Author + +Noyes, John S. + + + +Author + +Livermore, Laurence + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8013 +8013 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8013 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8013 +1314-2828--8013 + + + + +Pteroptrix longiclava (Girault, 1915) + + + + +Apteroptrix longiclava +Girault, 1915 + + +longicornis +Nikol'skaya, 1959 + + + +Distribution +England + + + \ No newline at end of file diff --git a/data/38/C1/42/38C142BD3B275A2590166470739D1001.xml b/data/38/C1/42/38C142BD3B275A2590166470739D1001.xml new file mode 100644 index 00000000000..04690b13a3f --- /dev/null +++ b/data/38/C1/42/38C142BD3B275A2590166470739D1001.xml @@ -0,0 +1,72 @@ + + + +Diversity of an Odonata assemblage from a tropical dry forest in San Buenaventura, Jalisco, Mexico (Insecta, Odonata) + + + +Author + +Gonzalez Soriano, Enrique +Departamento de Zoologia, Instituto de Biologia, Universidad Nacional Autonoma de Mexico, Mexico City, Mexico +esoriano@ib.unam.mx + + + +Author + +Noguera, Felipe +https://orcid.org/0000-0003-4417-8436 +Estacion de Biologia Chamela, Instituto de Biologia, Universidad Nacional Autonoma de Mexico, San Patricio, Jalisco, Mexico + + + +Author + +Perez-Hernandez, Cisteil X +https://orcid.org/0000-0002-6698-2524 +Laboratorio de Ecologia de la Conducta, Facultad de Biologia, Universidad Michoacana de San Nicolas de Hidalgo, Morelia, Mexico + +text + + +Biodiversity Data Journal + + +2024 + +2024-02-23 + + +12 + + +116135 +116135 + + + + +http://dx.doi.org/10.3897/BDJ.12.e116135 + +journal article +http://dx.doi.org/10.3897/BDJ.12.e116135 +1314-2828-12-e116135 +59FE8C5E5FC45E64B6A50A96AC992F8F + + + + +Argia harknessi Calvert, 1899 + + + +Distribution +San Buenaventura, Las Higueras, Los Yesos, Jalisco, MX + + +Notes +Phenology in SBV: Nov (1), Dec (3), Jan (6), Feb (10), Mar (7), Apr (2), Jun (7), Jul (1), Aug (1), Sep (5), Oct (1) + + + \ No newline at end of file diff --git a/data/38/C1/61/38C161F9F7628892CBD7FABEA44F930D.xml b/data/38/C1/61/38C161F9F7628892CBD7FABEA44F930D.xml new file mode 100644 index 00000000000..2d4842a9435 --- /dev/null +++ b/data/38/C1/61/38C161F9F7628892CBD7FABEA44F930D.xml @@ -0,0 +1,159 @@ + + + +Order Rodentia - Family Muridae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 2 + + + +1189 +1531 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316535 + + + + + +Grammomys ibeanus +(Osgood 1910) + + + + + + + +[Grammomys] ibeanus +( +Osgood 1910 +) + +, + +Field +Mus +. Nat. Hist. Publ., Zool. Ser., 10: 8 + + +. + + + + +Type Locality: + +Kenya +, Molo. + + + + + +Vernacular Names: +East African Grammomys +. + + + + +Distribution: +From extreme NE +Zambia +(Nyika Plateau; +Ansell, 1978 +) and +Malawi +( +Ansell and Dowsett, 1988 +) north through highlands of E +Tanzania +( +Stanley et al., 1998 +; and specimens in +MCZ +) and +Kenya +to S +Sudan +( +Hollister, 1919 +; +Hutterer and Dieterlen, 1984 +). + + + + +Conservation: +IUCN +– Lower Risk (lc). + + + + +Discussion: +Morphological and geographic definition of + +G. ibeanus + +is unsatisfactory, particularly the extent of its distribution in +Tanzania +. +Hutterer and Dieterlen (1984) +treated + +ibeanus + +as a form of + +G. cometes + +, but the striking morphological distinctions between samples of + +ibeanus + +and the type series of + +cometes + +prompted our specific ranking of + +ibeanus + +(see also account of + +G. cometes + +). + + + + \ No newline at end of file diff --git a/data/38/C1/7D/38C17DD3478F56B7A94E38BF33B572AF.xml b/data/38/C1/7D/38C17DD3478F56B7A94E38BF33B572AF.xml new file mode 100644 index 00000000000..9d06c1261ae --- /dev/null +++ b/data/38/C1/7D/38C17DD3478F56B7A94E38BF33B572AF.xml @@ -0,0 +1,216 @@ + + + +A foundation monograph of Convolvulus L. (Convolvulaceae) + + + +Author + +Wood, John R. I. +Department of Plant Sciences, South Parks Road, University of Oxford, OX 1 3 RB, UK & Honorary Research Associate, Royal Botanic Gardens, Kew + + + +Author + +Williams, Bethany R. M. +Department of Plant Sciences, South Parks Road, University of Oxford, OX 1 3 RB, UK & Department of Life Sciences, Natural History Museum, Cromwell Road, London SW 7 5 BD, UK + + + +Author + +Mitchell, Thomas C. +Plant Biodiversity Research, Technische Universitaet Muenchen, Maximus-von-Imhof Forum 2, 85354 Freising, Germany + + + +Author + +Carine, Mark A. +Department of Life Sciences, Natural History Museum, Cromwell Road, London SW 7 5 BD, UK + + + +Author + +Harris, David J. +https://orcid.org/0000-0002-6801-2484 +Royal Botanic Garden Edinburgh, 20 A Inverleith Row, Edinburgh EH 3 5 LR, UK + + + +Author + +Scotland, Robert W. +Department of Plant Sciences, South Parks Road, University of Oxford, OX 1 3 RB, UK +robert.scotland@plants.ox.ac.uk + +text + + +PhytoKeys + + +2015 + +2015-06-18 + + +51 + + +1 +282 + + + + +http://dx.doi.org/10.3897/phytokeys.51.7104 + +journal article +http://dx.doi.org/10.3897/phytokeys.51.7104 +1314-2003-51-1 +E76E3938E216FF804849B803C469FE14 +576310 + + + + +155. + +Convolvulus suendermannii Bornm., Repert. Spec. Nov. Regni Veg. 43: 152. 1938. ( +Bornmueller +1938: 152). + + + + + +Convolvulus boissieri subsp. suendermannii +(Bornm.) Kuzmanov, Fl. Nar. Republ. Bulgariya 8: 451 (1982). ( +Kuzmanov 1982 +: 451). Type. Based on + +Convolvulus suendermannii + +Bornm. + + + +Type. + +Plant from Bulgaria, Ali Botush Mountain, cultivated in Berlin, + +Suendermann + +s.n. (holotype B!). + + + +Distinguishing features. + +Intermediate between + +Convolvulus boissieri + +and + +Convolvulus lineatus + +. Stems short, ascending; leaves sessile, obovate to oblanceolate, acute, cuneate to a broad base. + + + +Distribution. +Endemic to the area of Ali Botush Mountain, Bulgaria + + +Notes. + + + +Convolvulus +suendermannii + + +is an interesting plant. We agree with + +Sa'ad +(1967) + +that it has the appearance of + +Convolvulus lineatus + +but +Bornmueller's +comment that it lies in "apparent midposition" between + +Convolvulus lineatus + +and + +Convolvulus compactus + +is readily understandable because of its dwarf habit so it is not difficult to see why +Kuzmanov (1982) +treated it as +subsp. suendermannii +of + +Convolvulus boissieri + +. It might well represent the hybrid +Convolvulus lineatus +x +Convolvulus boissieri subsp. compactus +. What adds to the interest is the type locality, which is precisely the same place where + +Stoianov + +868 was collected. This is the plant whose identity troubled Turrill and +Stace (1971 +: 57). If this is indeed a hybrid or intermediate in some way between + +Convolvulus lineatus + +and +Convolvulus boissieri subsp. compactus +rather than a geographically anomalous population of +Convolvulus boissieri subsp. boissieri +, the geographical difficulties in +Stace's +infraspecific classification of + +Convolvulus boissieri + +disappear. Some support for this view is provided by the presence of a distinct peduncle-like stem in the part of + +Stoianov + +868 preserved in the envelope of the specimen at Kew. While the leaves are clearly those of + +Convolvulus boissieri + +the inflorescence is thus atypical of that species and similar to that of the type of + +Convolvulus suendermannii + +. Another specimen ( + +Velcev +et al. + +711 (W, E) from nearby Slavjanka appears to be the same taxon. Careful field observation is necessary to confirm whether or not + +Convolvulus suendermannii + +is a hybrid. [ +Strid 1991 +: 18-20]. + + + + \ No newline at end of file diff --git a/data/38/C1/83/38C183B0A1E4862DC0FD169365E7C4B2.xml b/data/38/C1/83/38C183B0A1E4862DC0FD169365E7C4B2.xml new file mode 100644 index 00000000000..baae4bb1738 --- /dev/null +++ b/data/38/C1/83/38C183B0A1E4862DC0FD169365E7C4B2.xml @@ -0,0 +1,81 @@ + + + +Catalogue of Texas spiders + + + +Author + +Dean, David Allen +Department of Entomology, Texas A & M University, College Station, Texas, United States of America +a-dean-ento@tamu.edu + +text + + +ZooKeys + + +2016 + +2016-03-02 + + +570 + + +1 +703 + + + + +http://dx.doi.org/10.3897/zookeys.570.6095 + +journal article +http://dx.doi.org/10.3897/zookeys.570.6095 +1313-2970-570-1 +CE0DA439F6F64DCF82255700A3C50098 +E376FF8EFFF1F22C326D1E0DFF8BFFDF +579094 + + + + + +Ebo +iviei Sauer & Platnick, 1972 + + + + + +Ebo iviei +[ +Sauer and Platnick 1972 +: 41, mf, desc. (figs 3-4, 16)] + + + +Distribution. +Brewster + + +Type. +Utah + + +Etymology. + +Person (The species is named in honor of the late Wilton Ivie, who collected the series from Utah and first recognized the species as new, +Sauer and Platnick 1972 +). + + + +Collection. +MSU + + + \ No newline at end of file diff --git a/data/38/C1/B8/38C1B8A92D9DFE00EF9C0CE0C8D11796.xml b/data/38/C1/B8/38C1B8A92D9DFE00EF9C0CE0C8D11796.xml new file mode 100644 index 00000000000..ed133dbd2aa --- /dev/null +++ b/data/38/C1/B8/38C1B8A92D9DFE00EF9C0CE0C8D11796.xml @@ -0,0 +1,65 @@ + + + +Catalogue of the hymenopterous insects in the collection of the British Museum. Part VI. Formicidae. + + + +Author + +Smith, F. + +text + +1858 +British Museum + +London + + + +http://antbase.org/ants/publications/8127/8127.pdf + +book +8127 +C86CFDBF-61D9-48EE-9C2E-325FC0462B10 + + + + +3 +. +Eciton vagans +. B.M. + + + + +Formica vagans, Oliv. +Encycl. Meth. vi. 501. + + +Eciton vagans, Smith +, Trans. Ent. Soc. Lond. iii. new ser. (worker major). + + +Eciton simillima, Smith +, Trans. Ent. Soc. Lond. iii. new ser. (worker minor). + + + +Hab. Brazil; Mexico. + + + +The +E. vagans +and +E. crassicornis +have been received from the same locality, and both are entirely of a reddish-brown colour, including the mandibles and legs; there can be little doubt of their belonging to the same species; in general form they resemble +E. hamata +, the large worker having similar elongated curved mandibles. + + + + \ No newline at end of file diff --git a/data/38/C2/38/38C238AD20C048D6FC28BED33197B400.xml b/data/38/C2/38/38C238AD20C048D6FC28BED33197B400.xml new file mode 100644 index 00000000000..73df1665056 --- /dev/null +++ b/data/38/C2/38/38C238AD20C048D6FC28BED33197B400.xml @@ -0,0 +1,85 @@ + + + +Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea + + + +Author + +Dale-Skey, Natalie + + + +Author + +Askew, Richard R. + + + +Author + +Noyes, John S. + + + +Author + +Livermore, Laurence + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8013 +8013 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8013 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8013 +1314-2828-4-8013 + + + + + +Ormyrus gratiosus ( +Foerster +, 1860) + + + + + +Monobaeus gratiosus +Foerster +, 1860 + + + +Distribution +England + + +Notes +See Fig. 12 for habitus + + + \ No newline at end of file diff --git a/data/38/C3/2E/38C32E6BE4B8F660CFC2891B86491BEA.xml b/data/38/C3/2E/38C32E6BE4B8F660CFC2891B86491BEA.xml new file mode 100644 index 00000000000..710bcbdf27d --- /dev/null +++ b/data/38/C3/2E/38C32E6BE4B8F660CFC2891B86491BEA.xml @@ -0,0 +1,52 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Papilio sinapis +[ +spec. nov. +] + + + + +P. D. alis integerrimis rotundatis albis immaculatis: apicibus fuscescentibus. +Fn. svec. +800. + + + + +Habitat in +Brassica & +affinibus. + + + + \ No newline at end of file diff --git a/data/38/C3/3A/38C33A185C7717E5972FFCCD21082371.xml b/data/38/C3/3A/38C33A185C7717E5972FFCCD21082371.xml new file mode 100644 index 00000000000..3a89b133b9d --- /dev/null +++ b/data/38/C3/3A/38C33A185C7717E5972FFCCD21082371.xml @@ -0,0 +1,177 @@ + + + +New reports, phylogenetic analysis, and a key to Lactarius Pers. in the Greater Yellowstone Ecosystem informed by molecular data + + + +Author + +Barge, Edward G. + + + +Author + +Cripps, Cathy L. + +text + + +MycoKeys + + +2016 + +15 + + +1 +58 + + + + +http://dx.doi.org/10.3897/mycokeys.15.9587 + +journal article +http://dx.doi.org/10.3897/mycokeys.15.9587 +1314-4049-15-1 + + + +Taxon classification Fungi Russulales Russulaceae + + + +6. +Lactarius pallidomarginatus Barge & C.L. Cripps +Figure 8 + + + + + +Lactarius +pallidomarginatus + +The following morphological description is from Colorado material which includes the holotype and all are listed in +Barge et al. (2016) + + + +Description. + +Pileus 20-50 mm in diameter, convex to broadly convex to plane with or without a depressed center, smooth, subviscid to dry, azonate, blotchy light tan to light brown, developing violet stains, lighter (to cream) toward margin; margin in +curved +when young, remaining so or becoming nearly straight in age. Lamellae adnate to subdecurrent, subdistant to slightly crowded, white to pale yellow-cream, staining violet where damaged. Stipe 10-40 +x +5-10 mm, equal to slightly clavate, smooth, dry, white to cream, staining violet where damaged, hollow. Context white to cream, staining violet where damaged. Latex scarce to undetectable, watery, white, staining tissue violet. Odor mild. Taste mild. + + +Basidiospores 8-10 +x +6.5-8 +µm +, Q = 1.1-1.4, broadly ellipsoid to ellipsoid; ornamentation forming an incomplete to dense reticulum. Pleuromacrocystidia 81.5-112 +x +9-10 +µm +, scarce to scattered, cylindrical to lanceolate; apex acute to moniliform. Cheilomacrocystidia 48-101.5 +x +7.5-13 +µm +, scattered, cylindrical to lanceolate; apex acute to moniliform. + + + +Ecology and distribution. + +Known from only a few alpine localities in the central and southern Rocky Mountains with +Salix planifolia +and possibly also +Salix glauca +, late summer. + + + +Specimens examined. + +U.S.A. WYOMING: Sublette County, Wind River Range, Union Peak, near +Salix glauca +, 22 Aug 1994, ZT5229 (MONT). + + + +Discussion. + +This species was recently described ( +Barge et al. 2016 +) from the alpine zone in Southern Colorado with +Salix +. It is tentatively included here because a collection morphologically matching the type was made by Dr Egon Horak from the Wind +River +Range of Wyoming (technically in the southern GYE) with +Salix glauca +. Interestingly, out of all of the species examined thus far, +Lactarius pallidomarginatus +appears most closely related to the bright yellow, violet-staining +Salix +associate +Lactarius aspideus +(Figure 2A), to which it bares little resemblance. + + +In the Rocky Mountains, +Lactarius pallidomarginatus +is most easily confused with +Lactarius nanus +, +Lactarius glyciosmus +, +Lactarius montanus +, and +Lactarius aff. brunneoviolaceus +. The basidiomes of +Lactarius nanus +do not stain violet where damaged and it produces basidiospores with thicker, more jagged ridges, and macrocystidia with more rounded apices (see +Barge et al. 2016 +). +Lactarius glyciosmus +also does not stain violet where damaged, it has an odor of coconut, slightly smaller basidiospores (7-9 +x +5-7 +µm +), and smaller cheilomacrocystidia (33-66 +x +5-9 +µm +). The closely related violet-staining +Lactarius montanus +produces basidiomes which are typically much more robust and stain green on the stipe and pileus surface with KOH. +Lactarius montanus +also has a strongly resinous odor and taste, and is mainly subalpine with conifers. See comments under +Lactarius aff. brunneoviolaceus +for features differentiating +Lactarius pallidomarginatus +from that taxon. See +Barge et al. (2016) +for features differentiating +Lactarius pallidomarginatus +from the European taxon +Lactarius pseudouvidus +Kuehner +. + + + +Figure 8. +Lactarius pallidomarginatus +. Collection EB0041 under +Salix planifolia +, San Juan Mountains, Colorado, USA. Scale bar: 2 cm. Photo by E. Barge. + + + + + \ No newline at end of file diff --git a/data/38/C3/77/38C37790018133CC36D7E2950D4395AD.xml b/data/38/C3/77/38C37790018133CC36D7E2950D4395AD.xml new file mode 100644 index 00000000000..43ee69d941c --- /dev/null +++ b/data/38/C3/77/38C37790018133CC36D7E2950D4395AD.xml @@ -0,0 +1,50 @@ + + + +Nematodes from terrestrial and freshwater habitats in the Arctic + + + +Author + +Holovachov, Oleksandr + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1165 +1165 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1165 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1165 +1314-2828--1165 + + + + +Diplogaster rivalis (Leydig, 1854) + + + +Notes + +Lena River estuary, Russia ( +Gagarin 2001b +). + + + + \ No newline at end of file diff --git a/data/38/C3/86/38C3869C47055F48A02728E050887B2E.xml b/data/38/C3/86/38C3869C47055F48A02728E050887B2E.xml new file mode 100644 index 00000000000..cf94cfd3e16 --- /dev/null +++ b/data/38/C3/86/38C3869C47055F48A02728E050887B2E.xml @@ -0,0 +1,264 @@ + + + +Catalog of the genus Cylindrepomus Blanchard (Coleoptera, Cerambycidae, Dorcaschematini) in the Philippines, with description of a new species from northern Mindanao + + + +Author + +Medina, Milton Norman D. +https://orcid.org/0000-0001-6858-8048 +Coleoptera Research Center, University of Mindanao, Davao City, Philippines +mnd_medina@umindanao.edu.ph + + + +Author + +Baul, Melbert James G. +Human Resources for Health Network, Department of Health Center for Health Development - Northern Mindanao, J. V. Serina Street, Carmen, Cagayan de Oro City, Philippines + + + +Author + +Cabras, Analyn A. +https://orcid.org/0000-0002-0980-1651 +Coleoptera Research Center, University of Mindanao, Davao City, Philippines + +text + + +ZooKeys + + +2022 + +2022-08-04 + + +1116 + + +23 +32 + + + + +http://dx.doi.org/10.3897/zookeys.1116.86906 + +journal article +http://dx.doi.org/10.3897/zookeys.1116.86906 +1313-2970-1116-23 +997F85710D224C8392C7F57610409705 +13DB99D595F159C89E143DC94DFC5F14 + + + + +Cylindrepomus ansihagani Medina & Cabras +sp. nov. + + + + +Fig. 1A-D + + + +Holotype + +(Fig. +1 +), male: Philippines - Mindanao / Northern Mindanao / Misamis Oriental III.2022 / local collector (MMCP), to be deposited at PNM. + + + +Figure 1. + +Cylindrepomus ansihagani + +sp. nov. male holotype, habitus +A +dorsal aspect +B +ventral aspect +C +frons +D +lateral aspect. + + + + +Other material examined. + + +Cylindrepomus bivitticollis + +Breuning, 1947, +holotype +male, NRM; + +C. sexlineatus + +Schultze, 1934, +holotype +female, MTKD. + + + +Description. + +Male. +Dimensions ( +n += 1): LB: 14.0 mm. WH: 2.0 mm. LG: 1.5 mm. LL: 1.0 mm. WL: 1.0 mm. LP: 3.0 mm. WP: 2.0 mm. LE: 8.5 mm. WEH: 3.0 mm. + + +Teguments +generally matt black, pro- and mesotibia reddish-brown near base; metatibia reddish-brown up to apical third; mid tarsus pale brown; hind tibia, tarsus, and claw light brown. Ventral side matt black, tomentose, covered with white recumbent pubescence on prosternum, prothorax, and abdomen. + + +Head and gena +tomentose, covered with black recumbent pubescence; genae with few erect black hairs at the side; vertex with two small bands of white recumbent pubescence. Eyes prominent, black, as long as wide. Antennae long and slender (except scape), more than twice the body length, matt black; scape bulbous, coarsely granulated, with recumbent white setae near base, 2 +x +longer than wide; 2nd antennomere wider than long; 3rd antennomere coarsely granulated, 2 +x +longer than each of antennomeres 4-11; 5th antennomere slightly granulated; antennomeres 6-11 finely granulated. + + +Pronotum +1.5 +x +wider than long, tomentose, covered with black recumbent hairs; with two narrow bands of white recumbent pubescence, one at the base shaped like an elongated diamond, the other one triangle-shaped and near the margin; apical margin lined with golden setae. + + +Prosternum +tomentose, covered with black recumbent hairs at middle and white recumbent setae at sides. Mesosternum and metasternum tomentose, covered with black and white recumbent setae. Mesepisternum and metepisternum tomentose, covered with white recumbent setae. 1st to 4th abdominal ventrites tomentose, covered with white and black recumbent setae with sparse golden setae at each side; pygidium tomentose, covered with full black recumbent setae, apex lined with golden hairs (Fig. +1B +). + + +Elytra +2.5 +x +longer than wide, with coarse, uniformly aligned punctatation; humeri slight recurved; suture and margin raised, slightly truncate along suture; apex lanceolate; with two thick bands of white recumbent pubescence, one at basal third longitudinal with apex expanded laterally, and one near the apex, narrowed toward the tip; a few tiny white spots near suture and margin at apical third. Scutellum tomentose, covered with white recumbent setae, obscuring surface (Fig. +1A +). + +Coxae tomentose, covered with whitish recumbent hairs; trochanters reddish-brown; tibia armed with two small spines at base (colored black on protibia and mesotibia, pale brown on metatibia). Profemur slightly recurved near base. + +Male genitalia +(Fig. +2 A-J +): Tegmen ~1.5 mm long; lateral lobes slender, ~0.1 mm long and 0.6 mm wide; base with a broad central lobe bearing fine setae; apex bearing numerous golden setae, ~0.2-0.6 mm long. Aedeagus ~2.0 mm long and 0.5 mm wide, slightly recurved and tapering towards apex. Endophallus ~6.0 mm long. + + + +Figure 2. + +Cylindrepomus ansihagani + +sp. nov. +A +genitalia, dorsal aspect +B +genitalia, lateral aspect +C +genitalia, ventral aspect +D +aedeagus, ventral aspect +E +aedeagus, dorsal aspect +F +aedeagus, lateral aspect +G +tegmen, dorsal aspect +H +tegmen, lateral aspect +I +tegmen, ventral aspect +J +tergite VIII. Abbreviation: +En +- Endophallus. + + + + +Diagnosis. + + +Cylindrepomus ansihagani + +sp. nov. is distinct from its Mindanao endemic congeners ( + +C. bivitticollis + +and + +C. sexlineatus + +) in having pronotum with two narrow bands of white recumbent pubescence, one at the base, shaped like an elongated diamond, the other a triangular band of white recumbent pubescence near the margin, while + +C. bivitticollis + +has pronotum with a complete, pale yellow longitudinal band on each side of the disc and + +C. sexlineatus + +has pronotum with a yellowish spot on each side at the base. + + + +Etymology. +This new species is named after Datu Ramil P. Ansihagan, the tribal chieftain of the Higaunon Tribe, for his efforts in protecting and preserving the remaining forests in Barangay Eureka Gingoog City, Philippines. + + + +Distribution of + +Cylindrepomus ansihagani + +sp. nov. + +Philippines: Mindanao: Northern Mindanao, Gingoog City. + + + +Notes on ecology, threats, and conservation of + +Cylindrepomus ansihagani + +sp. nov. + + +The species is known from a single specimen that was collected during the expedition. The species was collected at an elevation of approximately 1000-1100 m a.s.l. using hand nets along the boundary between an agro-ecosystem and a secondary forest. Most of the trees present are endemic species including but not limited to + +Shorea negrosensis + +(Red Lauan), + +Shorea contorta + +(White Lauan), and + +Quercus subsericea + +(Philippine Ulayan Tree), all of which are native to the Philippines and considered highly valued trees. + + +The current threat to the +species' +habitat is the continued conversion of the remaining secondary forests into agricultural lands. Farmers use various chemicals such as pesticides, herbicides, and fungicides that could affect the +species' +population There is a need to conduct more expeditions, covering more habitats, to find additional populations of this and other species. Hence, research identifying the exact species distribution, area of occupancy and the +species' +extent of occurrence is important as a guide in making a future IUCN Red List assessment of this endemic species. + + + + \ No newline at end of file diff --git a/data/38/C3/93/38C39386CE7BB42F145F5DB19BF9DA34.xml b/data/38/C3/93/38C39386CE7BB42F145F5DB19BF9DA34.xml new file mode 100644 index 00000000000..88f7a072b0a --- /dev/null +++ b/data/38/C3/93/38C39386CE7BB42F145F5DB19BF9DA34.xml @@ -0,0 +1,55 @@ + + + +Catalogue of hymenopterous insects collected by Mr. A. R. Wallace at the Islands of Aru and Key. + + + +Author + +Smith, F. + +text + + +Journal of the Proceedings of the Linnean Society of London, Zoology + + +1859 + +3 + + +132 +158 + + + + +http://antbase.org/ants/publications/10342/10342.pdf + +journal article +10342 +03D4C4E8-74F9-42F2-8FD1-00A6DC22903A + + + + +3. +Ponera parallela +. + + + +P. nigra, opaca; antennis, mandibulis, pedibus abdominisque apice ferrugineis. +Worker. Length 3 1 / 4 lines. Opake black; the antennae thick and scarcely as long as the thorax, their apex and the mandibles bright ferruginous; the legs somewhat obscure ferruginous, with the articulations much brighter; the head a little wider than the thorax and subovate; the thorax, node of the petiole, and the abdomen of nearly equal width, the abdomen being slightly the widest; the node of the petiole nearly quadrate; the apical margin of the first segment and base of the second slightly depressed. + + + +Hab. +Aru +. + + + + \ No newline at end of file diff --git a/data/38/C3/E3/38C3E3351E09AD418AEAA2A29D6D84DD.xml b/data/38/C3/E3/38C3E3351E09AD418AEAA2A29D6D84DD.xml new file mode 100644 index 00000000000..44b7d211be9 --- /dev/null +++ b/data/38/C3/E3/38C3E3351E09AD418AEAA2A29D6D84DD.xml @@ -0,0 +1,52 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Procellaria +[ +gen. nov. +] + + + + +Rostrum +edentulum, subcompressum: Mandibulis aequalibus: superiore apice adunca; inferiore apice compres- so-canaliculata. + + +Nares +cylindro supra basin rostri decumbente, truncato. + + +Pedes +palmati: ungue postico sessili absque digito. + + + + \ No newline at end of file diff --git a/data/38/C4/2E/38C42E080C29EC4DCB8122B0D2A12DC0.xml b/data/38/C4/2E/38C42E080C29EC4DCB8122B0D2A12DC0.xml new file mode 100644 index 00000000000..20885baf8f7 --- /dev/null +++ b/data/38/C4/2E/38C42E080C29EC4DCB8122B0D2A12DC0.xml @@ -0,0 +1,86 @@ + + + +Order Chiroptera - Family Phyllostomidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +395 +426 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Platalina +Thomas 1928 + + + + + + + +Platalina +Thomas 1928 + +, +Ann. Mag. Nat. Hist., ser. 10, 8: 120 + +. + + + + +Type Species: + +Platalina genovensium +Thomas 1928 + + + + + +Species and subspecies: +1 species: + + +Species + +Platalina genovensium +Thomas 1928 + + + + + \ No newline at end of file diff --git a/data/38/C4/EE/38C4EE786D2716C2E47FEDDEDF9BC400.xml b/data/38/C4/EE/38C4EE786D2716C2E47FEDDEDF9BC400.xml new file mode 100644 index 00000000000..f139d2f73b4 --- /dev/null +++ b/data/38/C4/EE/38C4EE786D2716C2E47FEDDEDF9BC400.xml @@ -0,0 +1,74 @@ + + + +Species plantarum: exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas + + + +Author + +Linnaeus, Carolus + +text + +1753 +Laurentius Salvius + +Stockholm + + + +https://doi.org/10.5962/bhl.title.669 + +book +10.5281/zenodo.3931989 +3931989 + + + + +Chaerophyllum bulbosum +, +spec. nov. + + + +2. Chaerophyllum caule laevi: geniculis tumidis. + +Chaerophyllum foliis supradecompositis: caulinis articulis laevibus superne incrassatis. +Hort. ups.64. + + +Chaerophyllum radice turbinata carnosa. +Hort. cliff. 102. Roy. lugdb. 112. + + +Cicutaria bulbosa. +Bauh. pin. 161. + + +Myrrhis foetens. +Riv. pent. 49. + + + + +Habitat in +Alsatia +, +Hungaria +, +Helvetia +. ♂ + + + + + +* +Floribus disci masculis. + + + + + \ No newline at end of file diff --git a/data/38/C5/09/38C5094B8074F1E7D7390FDFAF143704.xml b/data/38/C5/09/38C5094B8074F1E7D7390FDFAF143704.xml new file mode 100644 index 00000000000..22f810cf834 --- /dev/null +++ b/data/38/C5/09/38C5094B8074F1E7D7390FDFAF143704.xml @@ -0,0 +1,112 @@ + + + +A cybercatalogue of American sand fly types (Diptera, Psychodidae, Phlebotominae) deposited at the Natural History Museum, London + + + +Author + +Adams, Zoe J. O. + + + +Author + +Shimabukuro, Paloma Helena Fernandes + +text + + +Biodiversity Data Journal + + +2018 + +6 + + +24484 +24484 + + + + +http://dx.doi.org/10.3897/BDJ.6.e24484 + +journal article +http://dx.doi.org/10.3897/BDJ.6.e24484 +1314-2828--24484 + + + + +Micropygomyia cayennensis maciasi Fairchild & Hertig, 1948 + + + + +Phlebotomus cayennensis maciasi +Fairchild & Hertig, 1948 ( +Fairchild and Hertig 1948 +) + + + +Materials + + +Type status: +Paratype +. Occurrence: catalogNumber: +BMNHE1722035 +; sex: +Female +; Taxon: scientificName: Micropygomyia (Micropygomyia) cayennensismaciasi (Fairchild & Hertig, 1948); Location: country: +Mexico +; stateProvince: +Mexico +; municipality: Zumpango; locality: +Zumpango +; Event: eventRemarks: http://phlebotominaenhmtypes.myspecies.info/node/154; Record Level: institutionCode: +NHMUK +; basisOfRecord: Preserved Specimen + + +Type status: +Paratype +. Occurrence: catalogNumber: +BMNHE1722036 +; sex: +Female +; Taxon: scientificName: Micropygomyia (Micropygomyia) cayennensismaciasi (Fairchild & Hertig, 1948); Location: country: +Guatemala +; stateProvince: Escuintla; municipality: San +Jose +; locality: + +San +Jose + +; Event: eventDate: +06-03-45 +; eventRemarks: http://phlebotominaenhmtypes.myspecies.info/node/155; Record Level: institutionCode: +NHMUK +; basisOfRecord: Preserved Specimen + + + + +Distribution +Belize, Guatemala, Mexico + + +Notes + +Valid species in +Micropygomyia (Micropygomyia) +. + + + + \ No newline at end of file diff --git a/data/38/C5/17/38C5176A41F97E3942552E547308F9DE.xml b/data/38/C5/17/38C5176A41F97E3942552E547308F9DE.xml new file mode 100644 index 00000000000..c03a06fdf3d --- /dev/null +++ b/data/38/C5/17/38C5176A41F97E3942552E547308F9DE.xml @@ -0,0 +1,182 @@ + + + +Flora Helvetica - Saxifragaceae + + + +Author + +Konrad Lauber + + + +Author + +Gerhart Wagner + + + +Author + +Andreas Gygax + +text + + +2018 +Haupt Verlag + +Bern + + + +Flora Helvetica + + + +196 +212 + + + +book chapter +978-3-258-08047-5 + + + + + +Saxifraga cuneifolia +L. + + + + + +Artbeschreibung: +10-20 cm +hoch, mit zahlreichen Blattrosetten lockere Rasen bildend. +Blaetter +breit-spatelfoermig +, kahl, + +mit wenigen stumpfen +Zaehnen +und gelblichem, knorpeligem Rand + +, am Grund +keilfoermig + +in einen Stiel +verschmaelert + +, die +ueberwinternden +unterseits meist violett. +Bluetentragende +Staengel +aufrecht, +unbeblaettert +, mit 1-3 +bluetigen +Aesten +. + +Kronblaetter +weiss, meist mit einem orangeroten Fleck + +. +Kelchblaetter +2-4 mm +lang. + + + + +Bluetezeit +: 5-7 + + +Standort und Verbreitung in der Schweiz: Feuchte, schattige Felsen und +Bloecke +, Kalkmeidend / montan-subalpin / A, M am Alpenrand + + + + +Verbreitung global: Mittel- und +suedeuropaeisch + + + + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl FfeuchtLichtzahl LschattigSalzzeichen--
Reaktionszahl Rsauer (pH 3.5-6.5)Temperaturzahl Tunter-subalpin und ober-montan
+Naehrstoffzahl +N + +naehrstoffarm + +Kontinentalitaetszahl +K +subozeanisch (hohe Luftfeuchtigkeit, geringe Temperaturschwankungen, eher milde Winter)
+
+
+ + +Volksname Deutscher Name: + +Keilblaettriger +Steinbrech + +Nom +francais +: + +Saxifrage +a +feuilles en coin + +Nome italiano: +Sassifraga a foglie cuneate + + +
+
\ No newline at end of file diff --git a/data/38/C5/B7/38C5B7FF04CFC4D5DA8D695FB83D4B3A.xml b/data/38/C5/B7/38C5B7FF04CFC4D5DA8D695FB83D4B3A.xml new file mode 100644 index 00000000000..36efd4addfc --- /dev/null +++ b/data/38/C5/B7/38C5B7FF04CFC4D5DA8D695FB83D4B3A.xml @@ -0,0 +1,88 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part C) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +370 +473 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Centaurea isnardii +Linnaeus + +, + +Species Plantarum +2 + +: 916. 1753 + + +. + + + +"Habitat in Europa australi?" RCN: 6618. + + +Type not designated. + + + +Original material: [icon] in Isnard in +Mem +. Acad. Roy. Sci. Paris 1719: 164, t. 9. 1719 (seep. 119). + + + + +Current name: + + +Centaurea aspera + +L. subsp. + +aspera + + +( +Asteraceae +). + + + + \ No newline at end of file diff --git a/data/38/C5/B8/38C5B89B531E5708910F30514BB88EE0.xml b/data/38/C5/B8/38C5B89B531E5708910F30514BB88EE0.xml new file mode 100644 index 00000000000..1582180795e --- /dev/null +++ b/data/38/C5/B8/38C5B89B531E5708910F30514BB88EE0.xml @@ -0,0 +1,522 @@ + + + +A missing piece is found: a new species of Paepalanthus (Poales, Eriocaulaceae) and the puzzling relations of the campos rupestres mountaintop floras of eastern Minas Gerais, Brazil + + + +Author + +Rocha, Luiz Henrique +https://orcid.org/0009-0004-9444-8849 +Universidade Federal de São João del-Rei (UFSJ), Departamento de Ciências Exatas e Biológicas, CEP 35701 - 970, Sete Lagoas, Minas Gerais, Brazil + + + +Author + +Gonella, Paulo Minatel +0000-0001-8332-5326 +Universidade Federal de São João del-Rei (UFSJ), Departamento de Ciências Exatas e Biológicas, CEP 35701 - 970, Sete Lagoas, Minas Gerais, Brazil & Universidade Estadual Paulista (UNESP), Faculdade de Ciências, Departamento de Ciências Biológicas, CEP 17033 - 360, Bauru, São Paulo, Brazil + + + +Author + +Oliveira Andrino, Caroline +0000-0003-1107-5692 +Universidade de Brasília (UnB), campus Darcy Ribeiro, Departamento de Botânica, CEP 70910 - 900, Brasília, Distrito Federal, Brazil + +text + + +PhytoKeys + + +2024 + +2024-06-11 + + +242 + + +317 +332 + + + +journal article +10.3897/phytokeys.242.122824 + + + + + +Paepalanthus magnus +L. H. Rocha, Gonella & Andrino + +sp. nov. + + + + +Fig. 1 +, +2 +, +3 +, +4 +, +5 + + + + + +Type +. + + + +Brazil +. +Minas Gerais +: Conselheiro Pena, Serra do Padre Ângelo, Serra do Pinhão, Pico do Pinhão, + +19 ° 15 ' 21 " S +, +41 ° 34 ' 57.24 " W + +, +1500 m +elev., fl. & fr., +18 Apr 2022 +, + +P +. +M +. Gonella, +L +. +H +. Rocha, D. +R +. Couto, D. +P +. Cordeiro & +E +. +C +. Ribeiro 3402 + +( +holotype +: +UB +; +isotype +: +SPF +). + + + + +Diagnosis. + + +The new species is most similar to + +Paepalanthus regelianus +Körn. + +, with which it shares the pilose abaxial surface of the leaves. However, + +P. regelianus + +presents scapes that are about twice as long as the leaves and tomentose ( +vs. +scapes at least 3 times longer than the leaves, and glabrous in + +P. magnus + +) and involucral bracts with a glabrous abaxial surface and ciliated margin ( +vs. +pilose in + +P. magnus + +). Furthermore, the spathes of + +P. regelianus + +are shorter than its leaves, approximately half as long as the leaves ( +vs. +spathes about as long as the leaves), present uniformly distributed trichomes ( +vs. +along longitudinal nerves), and possess a short opening, no longer than +1 cm +long ( +vs. +opening distinctly longer, 2.5–6.0 cm long). + + + + + + + +Paepalanthus magnus + +A +habit +B +leaf apex +C +spathe, detail of the opening +D +capitula in dorsal (left) and ventral (right) view +E +involucral bract +F +floral bract +G +staminate flower in lateral view +H +staminate flower with sectioned corolla, exposing the stamens and pistillodes +I +pistillate flower in lateral view +J +pistillate flower with petals and sepals distended, exposing the gynoecium +K +seed with numerous appendices along the periclinal walls. Illustration by Klei Souza based on the holotype ( +P. M. Gonella et al. 3402 +). + + + + + +Description. + + +Terricolous or rupicolous perennial +herb +, 55.0– +94.5 cm +high. +Roots +fibrous. +Caudex +present. +Stem +aerial, elongate, erect, thick, surrounded by marcescent leaves, 6.5–35.0 cm long. +Leaves +rosulate, 14.3–27.0 × +0.4–1.6 cm +, linear-lanceolate, green, abaxial surface with trichomes ca. +4 mm +long along the marked nerves, adaxial surface smooth and glabrous, margins ciliate, apex acute, mucronate. +Inflorescences +solitary per subtending leaf, axillary. +Spathes +13.0–24.0 cm long, chartaceous, cylindrical, closed, abaxial surface pilose along the marked nerves (striate), adaxial (internal) surface glabrous, obliquely opened, opening 2.5–6.0 cm long, margin ciliate, apex acuminate. +Scapes +50.0–89.0 cm long, 1–21 per plant (rosette), 5 - costate, erect, glabrous, green to golden, free. +Capitula +5.0–15.0 mm diam., white. +Involucral bracts +in 7–9 series, ca. 1.7–3.8 × +1.3–2.1 mm +, ovate, castaneous, margin ciliate, abaxially pubescent, shorter than the flowers. +Floral bracts +ca. +3.5 mm +long, linear-lanceolate, pigmented, densely pilose in the apical half with uniseriate trichomes ca. +2 mm +long, margin ciliate. +Flowers +3 - merous, diclinous, arranged in concentric circles without clear organization. +Staminate flowers +ca. +3.5 mm +long; pedicels ca. +1 mm +long, pilose, with trichomes +2–2.5 mm +long; sepals ca. 2.5–3 × +1 mm +, oblanceolate, united in the base to up to 1 / 3 of length, castaneous with pigmentation concentrated in the center and becoming more translucent towards the margins, abaxial surface densely pilose in the apical 2 / 3, trichomes reducing in size towards the apex, adaxial surface glabrous, margin ciliate, apex acuminate; corolla tubular, ca. +2.5 mm +long, free lobes ca. +0.3 mm +long, entirely glabrous, hyaline; stamens epipetalous, filament ca. +1.5 mm +long, anther dorsifixed, ca. +0.3 mm +long; pistillodes papillose, ca. +1 mm +long. +Pistillate flowers +ca. +4.5 mm +long; pedicel ca. +0.5 mm +long, densely pilose with long trichomes; sepals ca. +3.5 mm +long, oblong, united only at the very base, castaneous with apex more strongly pigmented, adaxial surface glabrous, abaxial surface with apex slightly pilose, margin ciliate, apex acuminate-truncate; petals ca. +3 mm +long, hyaline, base slightly pigmented, narrow obovate, free, adaxial surface pilose, abaxial surface glabrous, margin ciliate, apex acute; gynoecium with stigmatic and nectariferous branches emerging at the same height in the column, stigmatic branches ca. +1 mm +long, apex bifid, nectariferous branches ca. +0.7 mm +long, apex papillose, ovary ca. +1 mm +diam, ovoid; +Seed +ca. 0.76 × +0.60 mm +ovoid to ellipsoid, reddish, hilum acute, micropile obtuse, with numerous appendices with truncate apex along the periclinal walls. + + + + +Etymology. + + +The epithet “ magnus ” derives from the Latin “ great ”, “ large ”. This epithet was selected to denote the characteristic of the species being large in size, contrasting with the majority of +Eriocaulaceae +species found in the region where it occurs but also a reference to its larger size compared to its putative closest taxa. + + + + +Distribution and habitat. + + + +Paepalanthus magnus + +is a microendemic species, found only at the top plateau of Pico do Pinhão ( +1540 m +a. s. l.), one of the highest peaks of Serra do Padre Ângelo, a mountain complex located in the municipality of Conselheiro Pena, eastern +Minas Gerais +, southeastern +Brazil +(Fig. +4 +). The species was found at elevations above +1500 m +a. s. l., forming a population of no more than 100 individuals growing directly on sandy soil among grasses or between large blocks of quartzitic rock, exposed to direct sunlight, in campos rupestres vegetation (Fig. +2 A, B +). + + + + + + + +Paepalanthus magnus + +A +habitat at Pico do Pinhão, with the Pico da Bela Adormecida (Pico do Padre Ângelo) in the background +B +habit among grasses and quartzitic rocks +C +rosette in detail +D +leaves, showing ciliate margin and striate abaxial surface +E +the base of the leaves, showing the adaxial surface and a scape enclosed by a spathe emerging from a leaf axil +F +spathe opening +G +capitulum in posterior view evidencing the involucral bracts +H +capitulum, lateral view +I +capitulum, frontal view. +A +by Lucian Medeiros +B – I +by PMG. + + + + + + + + +Paepalanthus magnus + +. +SEM +micrograph of the seed coat (from the holotype, +P. M. Gonella et al. 3402 +). + + + + + + + +Distribution maps +A +distribution map of the new species and compared taxa cited in the text +B +distribution map of + +P. magnus + +at Serra do Padre Ângelo region, with other landmarks of the region indicated. + + + +Pico do Pinhão is part of the northern massif of +SPA +, the Serra do Pinhão, whose culminating point is Pico do Sossego ( +1605 m +), to the northwest of Pico do Pinhão. Expeditions to the former failed to find new populations of the species, which were also not found in the other higher peaks of the region, such as Pico da Bela Adormecida (also known as Padre Ângelo; +1550 m +) and Pico da Aliança ( +1430 m +), reinforcing the microendemic character of the species. At Pico do Pinhão, the campos rupestres are found at elevations above +1300 m +. They are surrounded by a matrix of the Montane Seasonal Forest, which harbors the last individuals of the northernmost population of the endangered gymnosperm + +Araucaria angustifolia +(Bertol.) Kuntze ( +Moura 1975 +) + +, locally known as “ pinhão ” hence the name of the Serra. Such forest matrix, however, is severely degraded and is still subject to fires for land clearing and pasture formation (Fig. +5 +), as well as by the presence of cattle. The surrounding area is also severely invaded by alien species, especially the fern + +Pteridium aquilinum + +( +L +.) Kuhn ( +Dennstaedtiaceae +) and molasses grass + +Melinis minutiflora +P. Beauv. + +( +Poaceae +). + + + + + + +Conservation threats to + +Paepalanthus magnus + +A +35 - year fire record (1985–2020) in the region of Serra do Pinhão, part of Serra do Padre Ângelo +B +fire record in the year 2020 +C +land use of the region. Data on fire and land use from +MapBiomas (2024 +). +A +, +B +Map data © 2024 Google. + + + + + +Phenology. + +Specimens were collected with flowers and fruits in April, which is by the end of the rainy season. The presence of old inflorescences with viable fruits, however, suggests that the flowering may occur since the beginning of the rainy season, which in the region starts in October / November. + + + +Conservation status. + + +Preliminarily assessed as Critically Endangered – +CR +B +1 ab (iii) + +B +2 ab (iii). The species is known from a single location in an area that is not protected, and which is subject to several ongoing threats to the quality of the habitat, such as deforestation, the presence of cattle, recurrent use of fires, and the presence of invasive species. Furthermore, species restricted to mountaintop habitats are especially vulnerable to the effects of climate change, especially intense droughts that may cause increased mortality (already observed in other taxa in the region) or intense rainfalls, which may cause landslides (already reported in the +SPA +following intense rainfall in the 2021 / 2022 rainy season). Arson fires are especially recurrent in the southwest of Serra do Pinhão (Fig. +5 A +) and are used by local farmers to renovate pastures and clear land for coffee and + +Eucalyptus + +plantations. These fires, however, often escape to native vegetation, causing the observed reduction of forest remnants and the intensification of invasion by the aforementioned alien species. The last of these intense fire events was in 2020 (Fig. +5 B +), also the year of another intense fire affecting the Pico da Bela Adormecida and its species ( +Andrino and Gonella 2021 +; +Gonella et al. 2022 +; +Andrino et al. 2024 +). + + +Since the species is known from a single location, it has an estimated AOO of +4 km +2 +, and it does not have an associated EOO polygon, which, combined with the small population size and the listed ongoing threats, allow us to project a continuing decline in the quality of the habitat. Therefore, we suggest that the species should be declared Critically Endangered under the +IUCN (2012 +) criteria. This preliminary assessment will be submitted to the Brazilian Flora authority of the +IUCN +Red List, coordinated by Centro Nacional de Conservação da Flora (CNCFlora), for validation. + + + + + +Additional specimen examined ( +paratype +). + + + +Brazil +. +Minas Gerais +: Conselheiro Pena, Serra do Padre Ângelo, complexo Serra do Pinhão, Pico do Pinhão, +18 Apr 2022 +, + +D. +R +. Couto, +P +. +M +. Gonella, D. +P +. Cordeiro & +L +. +H +. Rocha-Pinto 6286 + +( +MBML +). + + + + \ No newline at end of file diff --git a/data/38/C5/D0/38C5D002FB2350B28001157E49CF892B.xml b/data/38/C5/D0/38C5D002FB2350B28001157E49CF892B.xml new file mode 100644 index 00000000000..b20d123f5f0 --- /dev/null +++ b/data/38/C5/D0/38C5D002FB2350B28001157E49CF892B.xml @@ -0,0 +1,92 @@ + + + +Diversity pattern of insects from Macao based on an updated species checklist after 25 years + + + +Author + +Xian, Chunlan +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China + + + +Author + +Leong, Chi Man +Department of Life Sciences, Faculty of Science and Technology, Beijing normal university - Hong Kong Baptist University United International College, Zhuhai, China & Macao Entomological Society, Estrada Coronel Nicolau de Mesquita, Macao SAR, China + + + +Author + +Luo, Jiuyang +https://orcid.org/0000-0002-2748-9534 +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China + + + +Author + +Jia, Fenglong +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China + + + +Author + +Han, Hongxiang +Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, China +hanhx@ioz.ac.cn + + + +Author + +Xie, Qiang +https://orcid.org/0000-0001-6376-8808 +School of Life Sciences, State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China +xieq8@mail.sysu.edu.cn + +text + + +Biodiversity Data Journal + + +2024 + +2024-04-05 + + +12 + + +118110 +118110 + + + + +http://dx.doi.org/10.3897/BDJ.12.e118110 + +journal article +http://dx.doi.org/10.3897/BDJ.12.e118110 +1314-2828-12-e118110 +57B0CE31B4055266A115FC1275D70C79 + + + + +Perissus indistinctus Gressitt, 1940 + + + +Notes + +Lin et al. (2021) + + + + \ No newline at end of file diff --git a/data/38/C5/D4/38C5D4EBF63AA3C366699FF15B17E4FD.xml b/data/38/C5/D4/38C5D4EBF63AA3C366699FF15B17E4FD.xml new file mode 100644 index 00000000000..166dcc512a4 --- /dev/null +++ b/data/38/C5/D4/38C5D4EBF63AA3C366699FF15B17E4FD.xml @@ -0,0 +1,64 @@ + + + +The Mecyclothorax beetles (Coleoptera, Carabidae, Moriomorphini) of Tahiti, Society Islands + + + +Author + +Liebherr, James K. + +text + + +ZooKeys + + +2013 + +322 + + +1 +170 + + + + +http://dx.doi.org/10.3897/zookeys.322.5492 + +journal article +http://dx.doi.org/10.3897/zookeys.322.5492 +1313-2970-322-1 + + + + +17. +Mecyclothorax altiusculoides Perrault, 1987: 425; 1988: 237 + + + +Identification. + +Like +Mecyclothorax hamatus +, but with the anterior transverse impression of the pronotum shallow, broad, and indistinct medially. The pronotal and lateral elytral depressions are broadly reflexed throughout their length (Fig. 16D). The discal elytral striae 1-4 are distinctly punctate in their basal half, the punctures expanding the striae. The eighth elytral interval is upraised and finely carinate dorsad the apical half of the posterior series of the lateral elytral setae, becoming broader and more convexly upraised apically. The frons is glossy with indistinct isodiametric to transverse sculpticells, and the vertex including the neck impression is covered with a regular mesh of isodiametric sculpticells in transverse rows. The pronotal disc is covered with a shallow but regular transverse mesh resulting in a subiridescent sheen, and the discal elytral intervals bear an isodiametric mesh, the sculpticells partially arranged in transverse rows. The male aedeagal median lobe is gracile, and the apex is gently expanded ventrally, moreso dorsally in the shape of a blunt tooth (Fig. 18E). The ostial canal is curved ventrally at its apical terminus. Setal formula 2122; standardized body length 5.8-7.0 mm. + + + + +Distribution +and habitat. + + +The type series ( +Perrault 1988 +) was composed of specimens variously recorded from localities ranging 1100-1400 m and 1000-1800 m elevation on Mont Aorai. Subsequent records include samples from decayed fronds of +Freycinetia +piled on the ground after trail clearing, and from beating live and dead fern fronds. These latter samples spanned 1255-1320 m elevation. + + + + \ No newline at end of file diff --git a/data/38/C6/4D/38C64D3D57EFB676091CDC45E40A7B59.xml b/data/38/C6/4D/38C64D3D57EFB676091CDC45E40A7B59.xml new file mode 100644 index 00000000000..308a3381211 --- /dev/null +++ b/data/38/C6/4D/38C64D3D57EFB676091CDC45E40A7B59.xml @@ -0,0 +1,833 @@ + + + +Biodiversity inventories in high gear: DNA barcoding facilitates a rapid biotic survey of a temperate nature reserve + + + +Author + +Telfer, Angela C +Biodiversity Institute of Ontario, Guelph, Canada +atelfer@uoguelph.ca + + + +Author + +Young, Monica R +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Quinn, Jenna +rare Charitable Research Reserve, Cambridge, Canada + + + +Author + +Perez, Kate +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Sobel, Crystal N +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Sones, Jayme E +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Levesque-Beaudin, Valerie +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Derbyshire, Rachael +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Fernandez-Triana, Jose +CNC, Ottawa, Canada +https://orcid.org/0000-0003-0425-0309 + + + +Author + +Rougerie, Rodolphe +Museum national d'Histoire Naturelle, Paris, France + + + +Author + +Thevanayagam, Abinah +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Boskovic, Adrian +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Borisenko, Alex V +Biodiversity Institute of Ontario, Guelph, Canada +https://orcid.org/0000-0002-3061-3057 + + + +Author + +Cadel, Alex +University of Waterloo, Waterloo, Canada + + + +Author + +Brown, Allison +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Pages, Anais +Universite de Montpellier, Montpellier, France + + + +Author + +Castillo, Anibal H +Biodiversity Institute of Ontario, Guelph, Canada +https://orcid.org/0000-0002-1537-0528 + + + +Author + +Nicolai, Annegret +EcoBio, Universite of Rennes, Rennes, France + + + +Author + +Glenn Mockford, Barb Mockford +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Bukowski, Belen +Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " (MACN-CONICET), Buenos Aires, Argentina + + + +Author + +Wilson, Bill +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Trojahn, Brock +rare Charitable Research Reserve, Cambridge, Canada + + + +Author + +Lacroix, Carole Ann +Biodiversity Institute of Ontario Herbarium, Guelph, Canada + + + +Author + +Brimblecombe, Chris +University of Waikato, Hamilton, New Zealand + + + +Author + +Hay, Christoper +University of Western Ontario, London, Canada + + + +Author + +Ho, Christmas +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Steinke, Claudia +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Warne, Connor P +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Garrido Cortes, Cristina +University of Guelph, Guelph, Canada + + + +Author + +Engelking, Daniel +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Wright, Danielle +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Lijtmaer, Dario A +Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " (MACN-CONICET), Buenos Aires, Argentina + + + +Author + +Gascoigne, David +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Hernandez Martich, David +Universidad Autonoma de Santo Domingo DR, Santo Domingo, Dominican Republic + + + +Author + +Morningstar, Derek +Myotistar, Cambridge, Canada + + + +Author + +Neumann, Dirk +SNSB, Zoologische Staatssammlung Muenchen, Munich, Germany + + + +Author + +Steinke, Dirk +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Marco DeBruin, Donna DeBruin +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Dobias, Dylan +University of Guelph, Guelph, Canada + + + +Author + +Sears, Elizabeth +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Richard, Ellen +University of Guelph, Guelph, Canada + + + +Author + +Damstra, Emily +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Zakharov, Evgeny V +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Laberge, Frederic +University of Guelph, Guelph, Canada + + + +Author + +Collins, Gemma E +University of Waikato, Hamilton, New Zealand + + + +Author + +Blagoev, Gergin A +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Grainge, Gerrie +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Ansell, Graham +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Meredith, Greg +Grand River Conservation Authority, Guelph, Canada + + + +Author + +Hogg, Ian +University of Waikato, Hamilton, New Zealand + + + +Author + +McKeown, Jaclyn +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Topan, Janet +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Bracey, Jason +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Guenther, Jerry +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Sills-Gilligan, Jesse +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Addesi, Joseph +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Persi, Joshua +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Layton, Kara K S +The University of Western Australia, Perth, Australia + + + +Author + +D'Souza, Kareina +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Dorji, Kencho +National Biodiversity Centre, Thimphu, Bhutan + + + +Author + +Grundy, Kevin +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Nghidinwa, Kirsti +Ministry of Environment and Tourism in Namibia, Windhoek, Namibia + + + +Author + +Ronnenberg, Kylee +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Lee, Kyung Min +University of Oulu, Oulu, Finland + + + +Author + +Xie, Linxi +The University of Western Ontario, London, Canada + + + +Author + +Lu, Liuqiong +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Penev, Lyubomir +Pensoft, Sofia, Bulgaria +https://orcid.org/0000-0002-2186-5033 + + + +Author + +Gonzalez, Mailyn +Instituto de Investigacion de Recursos Biologicos Alexander von Humboldt, Bogota, Colombia + + + +Author + +Rosati, Margaret E +Smithsonian National Museum of Natural History, Washington, United States of America + + + +Author + +Kekkonen, Mari +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Kuzmina, Maria +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Iskandar, Marianne +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Mutanen, Marko +University of Oulu, Oulu, Finland + + + +Author + +Fatahi, Maryam +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Pentinsaari, Mikko +University of Oulu, Oulu, Finland + + + +Author + +Bauman, Miriam +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Nikolova, Nadya +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Ivanova, Natalia V +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Jones, Nathaniel +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Weerasuriya, Nimalka +The University of Western Ontario, London, Canada + + + +Author + +Monkhouse, Norman +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Lavinia, Pablo D +Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " (MACN-CONICET), Buenos Aires, Argentina + + + +Author + +Jannetta, Paul +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Hanisch, Priscila E +Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " (MACN-CONICET), Buenos Aires, Argentina + + + +Author + +McMullin, R. Troy +Biodiversity Institute of Ontario Herbarium, Guelph, Canada + + + +Author + +Ojeda Flores, Rafael +Universidad Nacional Autonoma de Mexico, Mexico City, Mexico + + + +Author + +Mouttet, Raphaelle +ANSES, Laboratoire de la Sante des Vegetaux, Montferrier sur Lez, France + + + +Author + +Vender, Reid +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Labbee, Renee N +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Forsyth, Robert +New Brunswick Museum, Saint John, Canada +https://orcid.org/0000-0002-9637-0158 + + + +Author + +Lauder, Rob +London Homeopathy, London, Canada + + + +Author + +Dickson, Ross +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Kroft, Ruth +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Miller, Scott E +Smithsonian National Museum of Natural History, Washington, United States of America + + + +Author + +MacDonald, Shannon +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Panthi, Sishir +Ministry of Forests and Soil Conservation, Kathmandu, Nepal + + + +Author + +Pedersen, Stephanie +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Sobek-Swant, Stephanie +rare Charitable Research Reserve, Cambridge, Canada + + + +Author + +Naik, Suresh +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Lipinskaya, Tatsiana +Scientific and Practical Center for Bioresources, National Academy of Sciences of Belarus, Minsk, Belarus + + + +Author + +Eagalle, Thanushi +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Decaens, Thibaud +Universite de Montpellier Centre d'Ecologie Fonctionnelle et Evolutive, Montpellier, France + + + +Author + +Kosuth, Thibault +Universite de Montpellier, Montpellier, France + + + +Author + +Braukmann, Thomas +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Woodcock, Tom +rare Charitable Research Reserve, Cambridge, Canada + + + +Author + +Roslin, Tomas +University of Helsinki, Helsinki, Finland + + + +Author + +Zammit, Tony +Grand River Conservation Authority, Cambridge, Canada + + + +Author + +Campbell, Victoria +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Dinca, Vlad +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Peneva, Vlada +Bulgarian Academy of Sciences, Sofia, Bulgaria + + + +Author + +Hebert, Paul D N +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +deWaard, Jeremy R +Biodiversity Institute of Ontario, Guelph, Canada +dewaardj@uoguelph.ca + +text + + +Biodiversity Data Journal + + +2015 + +3 + + +6313 +6313 + + + + +http://dx.doi.org/10.3897/BDJ.3.e6313 + +journal article +http://dx.doi.org/10.3897/BDJ.3.e6313 +1314-2828-3-e6313 +FFE5FF837519E9253D17614AFFA8FFC1 +574474 + + + + +Polistes dominula Christ, 1791 + + + +Notes +BOLD:AAB7105 + + + \ No newline at end of file diff --git a/data/38/C6/88/38C688F081B8857F80E3CB1ED5C8DC75.xml b/data/38/C6/88/38C688F081B8857F80E3CB1ED5C8DC75.xml new file mode 100644 index 00000000000..40880e58fda --- /dev/null +++ b/data/38/C6/88/38C688F081B8857F80E3CB1ED5C8DC75.xml @@ -0,0 +1,153 @@ + + + +Parasitic copepods (Crustacea, Hexanauplia) on fishes from the lagoon flats of Palmyra Atoll, Central Pacific + + + +Author + +Soler-Jimenez, Lilia C. + + + +Author + +Morales-Serna, F. Neptali + + + +Author + +Aguirre-Macedo, Ma. Leopoldina + + + +Author + +McLaughlin, John P. + + + +Author + +Jaramillo, Alejandra G. + + + +Author + +Shaw, Jenny C. + + + +Author + +James, Anna K. + + + +Author + +Hechinger, Ryan F. + + + +Author + +Kuris, Armand M. + + + +Author + +Lafferty, Kevin D. + + + +Author + +Vidal-Martinez, Victor M. + +text + + +ZooKeys + + +2019 + +833 + + +85 +106 + + + + +http://dx.doi.org/10.3897/zookeys.833.30835 + +journal article +http://dx.doi.org/10.3897/zookeys.833.30835 +1313-2970-833-85 +6F31349BBF7D434D8C064128FDD76A56 + + + + +Nemesis sp. Risso, 1826 + + + +Current host. + +Carcharhinus melanopterus +( +Carcharhinidae +). + + + +Site of infection. +Gills. + + +Prevalence and mean intensity. + +40 and 2 ++/- +0.1 (n = 5). + + + +Specimens deposited. +CHCM No. 575 (voucher) (1 vial, 1 specimen ♀). + + +Remarks. + +Nemesis +is one of 12 genera in the family +Eudactylinidae +and includes about nine species ( +Mangena et al. 2014 +). +Nemesis +species can be divided into two groups by the relative width of the cephalothorax, free thoracic segments and genital segments ( +Dippenaar et al. 2008 +). One group (consisting of most of the species) has a fourth free thoracic segment that is much narrower than the preceding three, whereas the other (consisting of +N. lamna +only) has all four segments of about the same width ( +Kabata 1979 +). The identification and comparison of +Nemesis +species belonging to the first group is difficult because of morphological variation among individuals and the inconsistencies in the literature ( +Hewitt 1969 +, +Kabata 1979 +). + + + + \ No newline at end of file diff --git a/data/38/C6/B8/38C6B8AA687BC910E18C6A41E0292B49.xml b/data/38/C6/B8/38C6B8AA687BC910E18C6A41E0292B49.xml new file mode 100644 index 00000000000..8f7b67f90c8 --- /dev/null +++ b/data/38/C6/B8/38C6B8AA687BC910E18C6A41E0292B49.xml @@ -0,0 +1,76 @@ + + + +Oligosarcus perdido (Characiformes, Characidae), a new species of freshwater fish from Serra da Bodoquena, upper Rio Paraguai basin, Brazil. + + + +Author + +Alexandre C. Ribeiro + + + +Author + +Marcel R. Cavallaro + + + +Author + +Otávio Froehlich + +text + + +Zootaxa + + +2007 + +1560 + + +43 +53 + + + + +http://www.zoobank.org/urn:lsid:zoobank.org:pub:3779DDFF-75D8-49AF-96C8-18942ED78EE2 + +journal article +z01560p043 +3779DDFF-75D8-49AF-96C8-18942ED78EE2 + + + + +Oligosarcus schindleri +, + + + + + + +MZUSP +27923 + +, 2(c&s), + +Bolivia + +, + +Represa +Mexico +, 17 km, south of Cochabamba + +. + + + + + \ No newline at end of file diff --git a/data/38/C7/90/38C790923FF797EE083BB1D2F896120F.xml b/data/38/C7/90/38C790923FF797EE083BB1D2F896120F.xml new file mode 100644 index 00000000000..bceb43451ab --- /dev/null +++ b/data/38/C7/90/38C790923FF797EE083BB1D2F896120F.xml @@ -0,0 +1,131 @@ + + + +Contributions toward a reclassification of the Formicidae. Part VI. Ponerinae, tribe Ponerini, subtribe Odontomachiti. Section B. Genus Anochetus and bibliography. + + + +Author + +Brown, WL Jr., + +text + + +Studia Entomologica + + +1978 + +20 + + +549 +638 + + + + +http://antbase.org/ants/publications/6757/6757.pdf + +journal article +6757 + + + + +[41] +Anochetus mayri + + + + +Anochetus +of the mayri complex are the common small members of the genus in the New World, corresponding to +A. katonae +in Africa, and perhaps to +A. graeffei +in the Indo-Australian region. Like these species, +A. mayri +is variable in body size, eye size, antenna! scape length, color and sculpture, as well as size and details of form and dentition of the mandibles. It is not always easily separated from smaller specimens of the +inermis +complex on the one hand, or from +neglectus +on the other, and some of the variation raises the suspicion that +mayri +may include two or more sibling species. + + + +A +. mayri + +was first proposed in a key, without a proper description, from a specimen from St. Thomas ' in the West Indies. It was never described in full by Emery, so when Wheeler described the +subspecies laeviuscula +, he did not know what the +"typical" +mayri +was like. In fact, we still have no clear idea of what the color, sculpture, etc, of the +mayri +type really are, owing to the present difficulties of studying the material of the Emery Collection in Genoa. But we do know that the +mayri +complex is widespread in the West Indies and shows there wide variation in size, color and sculpture, including samples with predominantly smooth and some with completely striate pronota, as well as intermediates. After prolonged study of this material, I cannot find any way to separate it into two species, or even into reasonably clearcut geographical forms, so I assume that +mayri +and +laeviusculus +are synonyms. + +On the mainland, the situation is more complex, because the variation is more extensive. The Atlantic lowland forest of Costa Rica, for example, contains a larger, dark brown form (HL 1.05- 1.08, HW 0.92-0.94, ML 0.57-0.58, eye L 0.13 mm) with punctulate-striate sculpture weak in the middle of the pronotum, and weakly shining, but still not completely smooth. Sympatric in this area (for instance, at Rio Toro Amarillo, near Guapiles, Limon Prov.) is a smaller (HL 0.93, HW 0.82, ML 0.48, eye L 0.10-0.11 mm) brown- ish-yellow phenon with completely longitudinally striate pronotum. Whether these forms are conspecific or not cannot be decided without more evidence from this locality, but there are available intermediates among samples from elsewhere in the range, which extends from the Veracruz lowlands of Mexico through Central America and the West Indies to hylean South America, at least as far south as the Beni River drainage of Bolivia, and on the west slope of the Andes to southern Ecuador. + +South and east of the Amazon drainage in Brazil occurs a rather uniform mayri-complex phenon that is usually dull yellowish-brown in color, has finely striolate cephalic dorsum and sericeous-striolate or densely punctulate pronotum (the striation barely resolved at 50X). This form, which closely resembles certain variants from the West Indies, corresponds to the named varieties or +subspecies neglectus +, +australis +and +nobilis +, which I regard as synonyms. My instincts are to extend the synonymy by placing all 3 names under +mayri +, since no satisfactory characters have been found to separate +neglectus +from all samples of +mayri +, and this would be the preferred action here were it not for two stubborn facts: + + +First, the +neglectus +phenon is widespread and the only form over a wide area of central and southern Brazil, Uruguay and northern Argentina (and presumably Paraguay). It ranges at least from Pernambuco (Caruaru, B. Pickel), [central?] Mato Grosso, and Minas Gerais (Belo Horizonte, J. C. Bradley) southward to Santa +Fe +Prov. in N central Argentina. Over this range, the eyes are relatively fairly large (eye L 0.13-0.16 mm), and the mesopleura are sculptured throughout, though their lower middle portions are slightly shining. Most similar samples from the Caribbean area have smooth, shining areas on the mesopleura, and the eyes are smaller. + + +Second +, several males of undoubted +Anochetus +taken at light on 14 Nov. 1964 at Piracicaba, +Sao +Paulo State (C. Triplehorn), and about the right size to match mayri-complex workers, have terminalia radically different from those of males (figs. 70, 71) associated with mayri-complex workers taken in a nest from near Turrialba, Costa Rica (W. L. Brown). Males taken at light during June 1975 at Tinalandia, on the western slope of the Andes in Pichincha Prov., Ecuador (S. and J. Peck) are very similar to the Turrialba sample, at least as seen undissected. The Piracicaba males have broad-based, convex parameres that are suddenly constricted near midlength, and then each is continued as a slender, lanceolate, apical blade that is weakly concave facing laterad, so that when the terminalia are viewed end-on, the parameral apices are curved slightly away from the midline. The volsellae are also longer in the Piracicaba males, but the sharp apices of the aedeagal valves are shorter than those of the northern males. + + +We do not know for sure, of course, what kind of workers belong with the Piracicaba males, but the only right-sized workers that we know to occur in the area are those I call here +neglectus +. As long as there is a chance that these southern males do belong with +neglectus +workers, it will be necessary to recognize the latter name, even in the absence of absolute diagnostic characters for workers and queens. + + +As in other groups of +Anochetus +, the +mayri +complex will not be completely clarified until we have adequate samples of workers or queens associated in the nest with males. + + + + +A. mayri +is found mostly in forests under stones, in moss on rocks or logs, in rotten twigs on the forest floor, or in larger bodies of rotten wood. The workers and queen feign death, and are difficult to see. + + + + \ No newline at end of file diff --git a/data/38/C7/9D/38C79D70C2AD93CE6AB4ACC9E0C92E41.xml b/data/38/C7/9D/38C79D70C2AD93CE6AB4ACC9E0C92E41.xml new file mode 100644 index 00000000000..a453dc33e2c --- /dev/null +++ b/data/38/C7/9D/38C79D70C2AD93CE6AB4ACC9E0C92E41.xml @@ -0,0 +1,115 @@ + + + +Faunistic diversity of spiders (Araneae) in Galichitsa mountain (FYR Macedonia) + + + +Author + +Deltshev, Christo + + + +Author + +Komnenov, Marjan + + + +Author + +Blagoev, Gergin + + + +Author + +Georgiev, Teodor + + + +Author + +Lazarov, Stoyan + + + +Author + +Stojkoska, Emilija + + + +Author + +Naumova, Maria + +text + + +Biodiversity Data Journal + + +2013 + +1 + + +977 +977 + + + + +http://dx.doi.org/10.3897/BDJ.1.e977 + +journal article +http://dx.doi.org/10.3897/BDJ.1.e977 +1314-2828-1-977 + + + + +sisyphia +Phylloneta +Araneae +Arachnida +Arthropoda +Animalia + + + + +Phylloneta sisyphia (Clerk, 1757) + + + +Materials + + +Type status: +Other material +Occurrence: recordedBy: +C. Deltshev & M. Komnenov +; sex: +1 male +; Location: country: +FYR of Macedonia +; locality: +Galichitsa Mt., Simoncheska Lokva pool +; verbatimElevation: 1680 m; Event: eventDate: +18-06-2008 + + + + +Distribution +Palearctic. + + +Notes +First record in Galichitsa Mt. + + + \ No newline at end of file diff --git a/data/38/C7/A6/38C7A6E11A33A0E8A6C52D3B91971823.xml b/data/38/C7/A6/38C7A6E11A33A0E8A6C52D3B91971823.xml new file mode 100644 index 00000000000..313677ab340 --- /dev/null +++ b/data/38/C7/A6/38C7A6E11A33A0E8A6C52D3B91971823.xml @@ -0,0 +1,733 @@ + + + +Info Flora Schweiz - Asteraceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/asteraceae.html + +url + + + + + +Anthemis cotula +L. + + + + + +Stinkende Hundskamille + + + + +Art ISFS: 34800 Checklist: 1003890 +Asteraceae +Anthemis +Anthemis cotula L. + + + +Bestimmungsschluessel + + + +Zusammenfassung + + + + +Artbeschreibung + +(nach +Lauber & al. 2018 +) + +: +Aehnlich +wie + +A. arvensis + +, aber +unangenehm riechend +, +Spreublaetter +nur zwischen den innersten +Roehrenblueten +, sehr schmal, fast +borstenfoermig +(bei den andern +A.- +Arten auf dem ganzen +Bluetenboden +. Keine +Spreublaetter +bei den +aehnlichen + +Matricaria chamomilla +Nr. 2115 + +und + +Tripleurospermum inodorum +, Nr. 2117 + +), +Fruechte +undeutlich gerippt, aber meist dicht warzig, oft +druesig +. + + + + +Bluetezeit + +(nach +Lauber & al. 2018 +) + +: 5-10 + + +Standort und Verbreitung in der Schweiz + +(nach +Lauber & al. 2018 +) + +: +Aecker +, +Schuttplaetze +/ kollin-montan(-subalpin) / CH, sehr zerstreut + + + + +Verbreitung global + +(nach +Lauber & al. 2018 +) + +: +Urspruenglich +eurasiatisch + + + + +Oekologische +Zeigerwerte + +(nach +Landolt & al. 2010 +) + +243-444.t.2n=18 + + + +Status + + + +Status IUCN +: Stark +gefaehrdet + + + + +Nationale +Prioritaet +: 3 - Mittlere nationale +Prioritaet + + +Internationale Verantwortung +: 1 - Gering Erhalten/ +Foerdern +Gefaehrdungen +Ackerbau mit +Unkrautbekaempfung +, +unguenstiger +Fruchtfolge, zu dichtem Bestand der Kultur. Kleine, isolierte Vorkommen + + + +Oekologie + + +Lebensform Therophyt + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + + + + + +
+8.2.1.2 - Kalkreiche +Getreideaecker +( +Caucalidion +) +
+
+ + +fett + +Dominante Art, welche das Aussehen des Lebensraumes +mitpraegt + +Charakterart +Weniger strikt an den Lebensraum gebundene Art + + +
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +maessig +trocken +Lichtzahl LhellSalzzeichen--
Reaktionszahl Rneutral bis basisch (pH 5.5-8.5)Temperaturzahl T +kollin ( +Laubmischwaelder +mit Eichen) +
+Naehrstoffzahl +N + +maessig +naehrstoffarm +bis +maessig +naehrstoffreich + +Kontinentalitaetszahl +K +subkontinental (niedrige relative Luftfeuchtigkeit, grosse Temperaturschwankungen, eher kalte Winter)
+
+
+ + +Abhaengigkeit +vom Wasser + + + + + + + + + + + + + + + + + +
+Fluesse +0 - unbedeutend, keine Bindung.
Ruhiges Wasser0 - unbedeutend, keine Bindung.
Grundwasser0 - unbedeutend, keine Bindung.
+
+ +Nomenklatur + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Anthemis cotula +L. + + +
+ + +Volksname Deutscher Name: +Stinkende Hundskamille +Nom +francais +: + + +Anthemis + +fetide + +Nome italiano: +Camomilla fetida + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Anthemis cotula L. + + +Checklist 2017 + +34800
= +Anthemis cotula L. + + +Flora Helvetica 2001 + +2106
= +Anthemis cotula L. + + +Flora Helvetica 2012 + +2096
= +Anthemis cotula L. + + +Flora Helvetica 2018 + +2096
= +Anthemis cotula L. + + +Index synonymique 1996 + +34800
= +Anthemis cotula L. + + +Landolt 1977 + +3164
= +Anthemis cotula L. + + +Landolt 1991 + +2543
= +Anthemis cotula L. + + +SISF/ISFS 2 + +34800
= +Anthemis cotula L. + + +Welten & Sutter 1982 + +1779
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Status Indigenat +: Archeophyt: vor der Entdeckung von Amerika in der Region aufgetreten (vor 1500) + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein + + +Status Rote Liste national 2016 + + +Status IUCN +: Stark +gefaehrdet + + + +Zusaetzliche +Informationen + +Kriterien IUCN: B2ab(iii); C2a(i) + + +Status Rote Liste regional 2019 + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Biogeografische RegionenStatusKriterien IUCN
Jura (JU) +stark +gefaehrdet +(Endangered) +B2ab(iii); C2a(i)
Mittelland (MP) +stark +gefaehrdet +(Endangered) +B2ab(iii); C2a(i)
Alpennordflanke (NA) +stark +gefaehrdet +(Endangered) +B2ab(iii); C2a(i)
+Alpensuedflanke +(SA) +verschollen, vermutlich in der Schweiz ausgestorben (Critically Endangered, Probably Extinct)
+Oestliche +Zentralalpen (EA) +verschollen, vermutlich in der Schweiz ausgestorben (Critically Endangered, Probably Extinct)
Westliche Zentralalpen (WA)vom Aussterben bedroht (Critically Endangered)B2ab(iii); C2a(i)
+
+ + +Status nationale +Prioritaet +/Verantwortung + + + + + + + + + + + + + + + + + + + + + + +
+ +Nationale +Prioritaet + + +3 - Mittlere nationale +Prioritaet +
+Massnahmenbedarf + +1 - +Moeglicher +(unsicherer) Massnahmebedarf +
+ +Internationale Verantwortung + +1 - Gering
+ +Ueberwachung +Bestaende + + +0 - +Ueberwachung +ist nicht +noetig +
+
+ +Schutzstatus + + + + + + + + + + + + + + +
+International (Berner Konvention) +Nein
+GE + +Vollstaendig +geschuetzt +(25.07.2007)
+
+ + + + + + + + + + + + + +
+Schweiz +--
+VD + +Vollstaendig +geschuetzt +(02.03.2005)
+
+
+ + +Erhalten/ +Foerdern +Gefaehrdungen +und Massnahmen Ackerbau mit +Unkrautbekaempfung +, +unguenstiger +Fruchtfolge, zu dichtem Bestand der Kultur. Fruchtfolge mit 50% Getreideanteil Weder mechanische noch chemische +Unkrautbbekaempfung +waehrend +den Getreidejahren +Regelmaessige +Bodenbearbeitung mit Pflug Reduktion der +Stickstoffduengung +auf einen Drittel der empfohlenen Menge +fuer +die entsprechende Kultur +ueber +die ganze Fruchtfolge Gilt +fuer +alle Ackerbegleitpflanzen und die Finanzierung +fuer +die Landwirte ist +moeglich +als BFF, Typ 16 Kleine, isolierte Vorkommen +Regelmaessiges +Dokumentieren der Populationen Ex situ Kulturen in botanischen +Gaerten +anlegen (Erhaltungskulturen) und Ausbringung an Stellen, wo die Art +frueher +bekannt war Samen in einer nationalen Samenbank einlagern Mehr Informationen S. Schneider, 2017: Konzeption zum Schutz +gefaehrdeter +Ackerwildkraeuter +in Luxemburg, +Massnahmen +zum Erhalt - Vortrag auf dem Workshop Schutz der +gefaehrdeten +Ackerflora und -fauna, Bertrange. Organisiert von SICONA & Partnern S. Meyer et al, 2013: Ackerwildkrautschutz - Eine Bibliographie - BfN Skripten 351 J. Waymel & C. Zambettakis, 2015: +Declinaison +regionale +du plan national +d'actions +en faveur des plantes messicoles. Basse-Normandie 2015-2020. DREAL / REGION. Villers-Bocage: Conservatoire botanique national de Brest, 48 p + annexes J. Waymel, J. Buchet, C. Zambettakis, N. Valy, 2020: +Declinaison +regionale +du plan national +d'actions +en faveur des plantes messicoles (2015-2020); Liste des plantes messicoles de Normandie et Bilan des actions 2019.DREAL Normandie, +Region +Normandie: Con + + +
+
\ No newline at end of file diff --git a/data/38/C8/A7/38C8A7BFBB4E3CF6613948CF2EA19FF9.xml b/data/38/C8/A7/38C8A7BFBB4E3CF6613948CF2EA19FF9.xml new file mode 100644 index 00000000000..85a3c29a3a8 --- /dev/null +++ b/data/38/C8/A7/38C8A7BFBB4E3CF6613948CF2EA19FF9.xml @@ -0,0 +1,160 @@ + + + +Order Chiroptera - Family Pteropodidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +313 +350 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Pteropus admiralitatum +Thomas 1894 + + + + + + + +Pteropus admiralitatum +Thomas 1894 + +, +Ann. Mag. Nat. Hist., ser. 6, 13: 293 + +. + + + + +Type Locality: + +Papua New Guinea +, Bismarck Arch., Admiralty Isls. + + + + + +Vernacular Names: +Admiralty Flying Fox +. + + + + +Subspecies: +: + + +Subspecies + +Pteropus admiralitatum +subsp. +admiralitatum +Thomas 1894 + + + +Subspecies + +Pteropus admiralitatum +subsp. +colonus +K. Andersen 1908 + + + +Subspecies + +Pteropus admiralitatum +subsp. +goweri +Tate 1934 + + + +Subspecies + +Pteropus admiralitatum +subsp. +solomonis +Thomas 1904 + + + + + +Distribution: +Solomon Isls; Admiralty Isls, +New Britain +, and Tabar Isls (Bismarck Arch.). + + + + +Conservation: +CITES +– Appendix II. +IUCN +/ +SSC +Action Plan (1992) – +Not +Threatened. +IUCN +2003 – Lower Risk (lc). + + + + +Discussion: + +subniger + +species group. Reviewed by +Felten and Kock (1972) +; also see Flannery (1995 +b +) and +Bonaccorso (1998) +. + + + + \ No newline at end of file diff --git a/data/38/C8/D6/38C8D6C76E808AD5533C08A132B59EA5.xml b/data/38/C8/D6/38C8D6C76E808AD5533C08A132B59EA5.xml new file mode 100644 index 00000000000..ef29221527e --- /dev/null +++ b/data/38/C8/D6/38C8D6C76E808AD5533C08A132B59EA5.xml @@ -0,0 +1,109 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part T) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +878 +905 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Trifolium agrarium +Linnaeus + +, + +Species Plantarum 2 + +: 772. 1753 + + +, +nom. utique rej. + + + +"Habitat in Europae pratis." RCN: 5677. + + +Type not designated. + + + +Original material: + +Herb. Burser XVIII(2): 22 ( +UPS +) + +; + +Herb. Linn. No. 930.57 ( +LINN +) + +; + +Herb. Clifford: 374, + +Trifolium + +10, 3 sheets ( +BM +) + +; [icon] in Vaillant, Bot. Paris.: 196, t. 22, f. 3. 1727; [icon] in +Dodoens +, Stirp. Hist. Pempt., ed. 2: 576. 1616. + + + + +Current name: + + +Trifolium aureum + +Pollich + +( +Fabaceae +: +Faboideae +). + + + + \ No newline at end of file diff --git a/data/38/C9/1F/38C91F266F9699831442896781502AA6.xml b/data/38/C9/1F/38C91F266F9699831442896781502AA6.xml new file mode 100644 index 00000000000..7bcb7bca338 --- /dev/null +++ b/data/38/C9/1F/38C91F266F9699831442896781502AA6.xml @@ -0,0 +1,107 @@ + + + +Systematics of the family Ariidae (Ostariophysi, Siluriformes), with a redefinition of the genera. + + + +Author + +Alexandre P. Marceniuk + + + +Author + +Naércio A. Menezes + +text + + +Zootaxa + + +2007 + +1416 + + +1 +126 + + + + +http://www.zoobank.org/urn:lsid:zoobank.org:pub:FFC65592-D8DB-41BE-AEAC-A41EAB6C6185 + +journal article +z01416p001 + + + + +Hemiarius hardenbergi +(Kailola, 2000) + + + + +Arius hardenbergi +Kailola, 2000: 137, figs. 7-8. + +Type locality: +Maimeri River +, +2°06’S +, +133°45’E +, +Bintuni Bay +, +Papua (Irian Jaya) +. +Holotype +: + +WAM +P.29966-001 + + +. + +Paratypes +: + +AMS +I.29291-001 + + +, + + +NCIP +436 + + +, + + +QM +I.26088 + + +. + + + +Distribution: Southern New Guinea. +Countries: Papua New Guinea. + + +Habitat: Marine and brackish waters. + + +Maximum size: 260 mm SL. + + + \ No newline at end of file diff --git a/data/38/C9/3E/38C93E698DF1851EB18EEEE1AC949BCB.xml b/data/38/C9/3E/38C93E698DF1851EB18EEEE1AC949BCB.xml new file mode 100644 index 00000000000..6a63767bd60 --- /dev/null +++ b/data/38/C9/3E/38C93E698DF1851EB18EEEE1AC949BCB.xml @@ -0,0 +1,68 @@ + + + +Guide to the littoral zone vascular flora of Carolina bay lakes (U. S. A.) + + + +Author + +Howell, Nathan + + + +Author + +Krings, Alexander + + + +Author + +Braham, Richard R + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +7964 +7964 + + + + +http://dx.doi.org/10.3897/BDJ.4.e7964 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e7964 +1314-2828-4-7964 + + + + +Cyperus erythrorhizos Muhl. + + + + +Cyperus erythrorhizos +Taxon concept: [= RAB, GW, FNA, Weakley] + + + +Distribution +Horseshoe Lake: Buell 2263 (DUKE!); Rothfels, Burge, Duke Natural History Society 2403 (DUKE!) + + +Notes +Annual herbs. floating bogs; saturated, acidic, peaty soil (FB). Jul−Sep. Fig. 41 + + + \ No newline at end of file diff --git a/data/38/C9/A5/38C9A54BE04D144511B188DD0CA12F29.xml b/data/38/C9/A5/38C9A54BE04D144511B188DD0CA12F29.xml new file mode 100644 index 00000000000..12d5037ca6a --- /dev/null +++ b/data/38/C9/A5/38C9A54BE04D144511B188DD0CA12F29.xml @@ -0,0 +1,279 @@ + + + +Ophioderma peruana, a new species of brittlestar (Echinodermata, Ophiuroidea, Ophiodermatidae) from the Peruvian coast + + + +Author + +Pineda-Enriquez, Tania + + + +Author + +Solis-Marin, Francisco A. + + + +Author + +Hooker, Yuri + + + +Author + +Alfredo Laguarda-Figueras, + +text + + +ZooKeys + + +2013 + +357 + + +53 +65 + + + + +http://dx.doi.org/10.3897/zookeys.357.6176 + +journal article +http://dx.doi.org/10.3897/zookeys.357.6176 +1313-2970-357-53 +6455E2A2D4124DEF816AA49410923991 +6455E2A2D4124DEF816AA49410923991 + + + + + +Ophioderma +peruana +Pineda-Enriquez +, +Solis-Marin +, Hooker & Laguarda-Figueras + +sp. n. + + + +Type specimen. + +Holotype, CZA-363, Lobos de Afuera Island, Peru, +6°56'16.8"S +, +80°43'22.7"W +, intertidal, under rocks, October 9th, 2007. + + + +Type locality. + +Peru: Lobos de Afuera Island, +6°56'16.8"S +, +80°43'22.7"W +, intertidal, under rocks, October 9th, 2007. + + + +Other type material. + +Paratype, CZA-364, Lobos de Afuera Island, Peru, +6°56'16.8"S +, +80°43'22.7"W +, intertidal, October 9th, 2007; paratype, CZA-365, Lobos de Afuera Island, Peru, +6°56'16.8"S +, +80°43'22.7"W +, intertidal, October 9th, 2007; paratype, UNAM-ICML 3.234.0, Lobos de Afuera Island, Peru, +6°56'16.8"S +, +80°43'22.7"W +, intertidal, under rocks, October 9th, 2007 (Fig. 2). + + + +Figure 2. +Ophioderma peruana +sp. n., holotype (CZA-363). A aboral view B oral view C aboral disc and basal portion of the arms D oral disc and basal portion of the arms E jaws F oral portion of the disc and pair of genital slits. + + + + +Diagnosis. +Disc pentagonal, elevated and covered with dense granules that are somewhat rounded or polygonal, but more or less dispersed. The radial shields can be completely covered by the granules or scarcely covered. The dorsal arm plates are fragmented; in addition there are some smaller and tiny fragments that resembles granules of the dorsal disc, only visible on the proximal plates (not evident in all the arm segments). Nine or ten flattened and elongated oral papillae. Granules also cover the adoral shields. Ten arm spines, the ventral is the largest, reaching the next tentacle scale. + + +Description of holotype. +CZA-363: disc diameter 36.3 mm, arm length 120.6 mm, arm width 7.6 mm (Fig. 2). +Disc. Disc pentagonal, broad and flat, covered by granules; the dorsal granules are closely packed and have the same size on the middle and periphery of the disc, these granules are rounded and polygonal. The radial shields are almost fully covered by granules with only a small section exposed; the size is 3.81 mm and fit 9.5 times the disc diameter; the disc scales are small and imbricated, oval shape with polygonal borders, the interradial scales are smaller than the radial ones. Jaws with seven to nine oral papillae; the two distal ones are stout and longer than broad. The oral papillae have rounded edges and are almost of the same size and shape. The oral shields are broader than long, triangular in shape with convex proximal sides and are surrounded by granules that are slightly larger than those on the interradial disc surface. The adoral shields are rectangular and covered by larger and taller granules than those on the dorsal disc, which are contiguous. Four genital slits on each interradii; the two proximal ones are touching the oral shield and are located between the distal part of the oral shields and the first lateral arm plate; the two distal genital slits are placed between the fifth and and the sixth arm segment and close to the periphery of the disc. + +Arms. The basal portion of the arm is 7.6 mm broad and the arm length is 120.6 mm. The dorsal arm plates occupy less than 1/4 of the arm, are 4.6 times wider than long and rectangular, fragmented in six pieces that differ in shape; there are some granules on the proximal portion and sparcely distributed on the distal portion. The +lateral +arm plates have a half-circle shape, and occupy a sub-ventral position; with ten arm spines conical, large and slightly flattened with a rounded tip, half segment length decreasing slightly in size dorsally. The ventral-most arm spine is the longest and widest, almost the size of the segment. The ventral arm plates are contiguous, broader than long, the proximal plates are elongated in comparison to the distal plates. Two tentacle scales on each side of the ventral plate; the adradial tentacle scale is oval in shape, twice as long as wide and the abradial tentacle scale triangular in shape, with the straight side touching the ventral arm plate (Fig. 3). + + + +Figure 3. +Ophioderma peruana +sp. n., holotype (CZA-363). A basal portion of the arms with fragmented dorsal arm plates B dorsal arm plates fragmented in several pieces C ventral arm plates and tentacle scales D lateral view of the arm spines. + + +Color. Specimen preserved in alcohol. The dorsal side of the disc is light brown and the arms are darker brown, the dorsal arm plates of each segment are ornamented with a double row of tiny, whitish, rounded spots; the spines are brown except the two ventral ones that are cream color, like the ventral side of the arms; the jaws are white; the ventral side of the disc in the proximal part is white and the distal part is slightly darker; the oral shields are mottled. Dry specimens, have the dorsal side of the disc pale brown, the arms are brown with black and white spots; the tentacle feet are yellowish. Live specimens in the field could be identified by this color pattern: the dorsal side of the disc is brown with the disc granules lighter cream and brown; the arms are mottled with whitish spots; the ventral disc interradii are brown and arms under the disc are bright yellow. + +Paratype variations. Onthe smallest specimen (14 mm DD; 35 mm AL; 4 mm AW) the radial shields are completely naked with white spots (same color pattern as +the +dorsal arm plates), oval and surrounded by the disc granules by the disc granules, scarcely covered (in specimens with 40-42 mm DD) or completely naked (in specimens with14-35 mm DD). On certain segments of the arm, the dorsal arm plates are not as fragmented, with only two or three pieces. The presence of granules along the arm is not evident as in the holotype. In some specimens (22-31 mm DD) the radial shields are also completely naked. The oral shields are twice as wide as long, proximally elongated but the shape may vary in specimens. In two specimens (30 mm; 42 mm DD) the radial +shields +are naked and/or covered by granules. The radial shields are completely covered by granules and dorsal arm plates are fragmented in only a single specimen (35 mm DD) (Fig. 4). Therefore, as the animal grows, the radial shields become more covered in granules and the dorsal arm plates are fragment further. + + + +Figure 4. +Ophioderma peruana +sp. n.non-type preserved material (alcohol) showing different colors variations. A specimen in situB CZA-394 (14 mm DD) radial shields naked C CZA-392 (28 mm DD) radial shields naked D CZA-390 (35 mm DD) radial shields covered by disc granules. + + + + +Distribution. + +Only known from the coast of Peru. Lobos de Afuera Island, Lambayeque, Peru; intertidal (type locality); Quebrada Verde, El +Nuro +, Peru, 9 m; +4°13'39.3"S +, +81°12'30.0"W +and Hooker Reef, Punta Sal, Peru; 14 m; +3°57'14.20"S +, +80°57'48.50"W +(Fig. 1). + + + +Etymology. +Named after the type locality. + + +Remarks. +The new species is distinguishable by its thick and rounded granules on the disc, the number of fragments of the dorsal arm plates, which can be more than six with other smaller fragments. The distal border of the dorsal arm plates, from the base to the middle part of the arm, supports some granules similar to those on the dorsal part of the disc. + +In Peruvian waters, + +Ophioderma +panamensis + +and +Ophioderma teres +are found on the same localities, in addition tothe new species; it differs from other Peruvian species in shape and size of the tentacle scales and in the shape of the arm spines. It differs from +Ophioderma teres +by the smaller size and density of the granules on the disc. These granules are similar to those present on +Ophioderma sodipallaresi +, the main difference is that on the latter species they are somewhat more scattered than in +Ophioderma teres +, while in +Ophioderma peruana +sp. n. the dorsal granules are closely packed and have the same size on the middle and periphery of the disc, being rounded and polygonal. +Ophioderma sodipallaresi +differs in havingonly two to three fragments, whereas +Ophioderma teres +have a similar number to +Ophioderma peruana +sp. n. The shape and size of the tentacle scales in +Ophioderma teres +are similar to +Ophioderma peruana +sp. n., oval and elongated, whereas in +Ophioderma sodipallaresi +the abradial tentacle scale is longer than wide and the adradial scale is smaller, almost triangular or oval. The ventralmost arm spines are largest in all three species, and the others increase in size from dorsal to ventral. In +Ophioderma peruana +sp. n. the arm spines are thick and conical, similar to +Ophioderma sodipallaresi +, which are pointed, thick and short, but differing in size. Meanwhile, in +Ophioderma teres +the arm spines are almost flat with pointed tips. In comparison with the other West Pacific ophiodermatids species, +Ophioderma panamensis +and +Ophioderma vansyoci +differs from +Ophioderma peruana +sp. n. by presenting the radial shields naked, just bordered by the granulation of the disc; in contrast with +Ophioderma variegata +and +Ophioderma pentacantha +that has the radial shields covered by the disc granules, while in +Ophioderma peruana +sp. n. the radial shields could be naked or covered by the granules. +Ophioderma vansyoci +presents the dorsal arm plates fragmented in three pieces. The number of arm spines are variable, +Ophioderma pentacantha +has five, +Ophioderma vansyoci +has seven, +Ophioderma panamensis +and +Ophioderma variegata +has eight, while +Ophioderma peruana +sp. n. presents ten, +Ophioderma sodipallaresi +seven arm spines and +Ophioderma teres +nine arm spines. +Ophioderma variegata +and +Ophioderma pentacantha +presents the adoral shields slightly naked, in comparison with +Ophioderma panamensis +, +Ophioderma vansyoci +, +Ophioderma sodipallaresi +, +Ophioderma teres +and +Ophioderma peruana +sp. n. that presents the adoral shields covered by the disc granules. Among its congeners in the Caribbean Sea, +Ophioderma peruana +sp. n. is more similar to +Ophioderma squamosissima +and +Ophioderma guttata +sharing fragmented dorsal arm plates (more than six pieces) but differs from the later ones in the absence of the smaller scales on the dorsal arm plates, by having different shape of disc granules (rounded and polygonal in +Ophioderma peruana +sp. n., flattened, elongated and polygonal shape in +Ophioderma squamosissima +and flattened, shorter and polygonal in +Ophioderma guttata +), in addition to its geographic distribution. The rest of the +Ophioderma +species distributed in the Caribbean Sea either lacks fragmented arm plates ( +Ophioderma appressa +, +Ophioderma brevicauda +, +Ophioderma brevispina +, +Ophioderma phoenium +and +Ophioderma rubicunda +) or some segments of the dorsal arm plates could be fragmented ( +Ophioderma cinerea +). + + + + \ No newline at end of file diff --git a/data/38/C9/F6/38C9F64C5DE960848D381EE93ECF55A7.xml b/data/38/C9/F6/38C9F64C5DE960848D381EE93ECF55A7.xml new file mode 100644 index 00000000000..7c6422f5565 --- /dev/null +++ b/data/38/C9/F6/38C9F64C5DE960848D381EE93ECF55A7.xml @@ -0,0 +1,97 @@ + + + +Male sleeping aggregation of multiple Eucerini bee genera (Hymenoptera: Apidae) in Chapada Diamantina, Bahia, Brazil + + + +Author + +Mahlmann, Thiago + + + +Author + +Hipolito, Juliana + + + +Author + +de Oliveira, Favizia F. + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1556 +1556 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1556 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1556 +1314-2828--1556 + + + + +Melissodes (Ecplectica) nigroaenea (Smith, 1854) + + + +Materials + + +Type status: +Other material +. Occurrence: catalogNumber: +INPA s/n +; recordNumber: s/n; recordedBy: +T.Mahlmann et al. +; individualCount: +2 +; sex: +male +; lifeStage: +adult +; behavior: 03 males sleeping on dried flower; establishmentMeans: native; preparations: pinned; disposition: good; Taxon: taxonID: Native; scientificName: Melissodesnigroaenea; acceptedNameUsage: Melissodes (Ecplectica) nigroaenea (Smith, 1854); kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Apidae; genus: Melissodes; subgenus: Ecplectica; specificEpithet: nigroaenea; taxonRank: species; scientificNameAuthorship: (Smith, 1854); Location: continent: South America; country: +Brazil +; countryCode: BRA; stateProvince: Bahia; municipality: Ventura; locality: + +Chapada Diamantina, Morro do +Chapeu + +; locationRemarks: label transliteration: "BRA, Bahia, Morro do +Chapeu +, Ventura, 29.i.2011; 15h30; 11°40′10.4″S; 40°58′12″W, T.Mahlmann & J. +Hipolito +Leg."; "03 males sleeping on dried flower": Lamiaceae, aff. Hyptis sp."; verbatimCoordinates: 11°40′10.4″S 40°58′12″W; decimalLatitude: +-11.669556 +; decimalLongitude: +-40.970000 +; georeferenceProtocol: GPS; Identification: identifiedBy: +T.Mahlmann +; dateIdentified: 2014; Event: samplingProtocol: +sweeping +; eventDate: 2011. +i.29 +; eventTime: 15h30; year: 2011; month: 1; day: 29; Record Level: language: pt; collectionCode: +Insects +; basisOfRecord: PreservedSpecimen + + + + + \ No newline at end of file diff --git a/data/38/CA/16/38CA16AF48CBFE5B3FB9B3832F8A72B3.xml b/data/38/CA/16/38CA16AF48CBFE5B3FB9B3832F8A72B3.xml new file mode 100644 index 00000000000..4878e241aa7 --- /dev/null +++ b/data/38/CA/16/38CA16AF48CBFE5B3FB9B3832F8A72B3.xml @@ -0,0 +1,201 @@ + + + +A revision of the shore-fly genus Lamproclasiopa Hendel (Diptera, Ephydridae) + + + +Author + +Costa, Daniel N. R. + + + +Author + +Mathis, Wayne N. + + + +Author + +Marinoni, Luciane + +text + + +ZooKeys + + +2016 + +631 + + +1 +99 + + + + +http://dx.doi.org/10.3897/zookeys.631.10718 + +journal article +http://dx.doi.org/10.3897/zookeys.631.10718 +1313-2970-631-1 +FB2CA1FF5A5A4168AB6BA8ABD0CCD7B4 +FB2CA1FF5A5A4168AB6BA8ABD0CCD7B4 + + + +Taxon classification Animalia Diptera Ephydridae + + + +Lamproclasiopa triangularis +sp. n. +Figs 18-19, 20-23, 81 + + + + +Diagnosis +. + + +This species is distinguished from other congeners by the following combination of characters: Small to moderately small shore-fly species, body length 1.65-2.10 mm; generally black, subshiny to shiny. Head: Frons generally mostly brownish black to black, moderately microtomentose, subshiny; mesofrons more microtomentose, tan to brown; some specimens with 2 gray spots along ventral margin just dorsad of antennal bases. Antenna mostly black, especially scape and pedicel, only basal flagellomere with ventrobasal area with some yellow to yellowish orange coloration. Ventral half of face with a microtomentose triangle (Fig. 18), sometimes dorsal angle of triangle extended dorsally to level of base of antennae, base of triangle sometimes partially bare, otherwise face largely bare, black except for yellow to yellowish orange lateral margins adjacent to parafacial and antennal grooves; bearing 2 larger facial setae, dorsal seta at about midfacial height, dorsomesoclinate; ventral seta just dorsad of epistomal margin, slightly dorsoclinate; parafacial silvery white. Gena relatively short, gena-to-eye +ratio +0.06-0.10. Thorax: Mesonotum uniformly whitish gray microtomentose; pleural area very sparsely microtomentose, mostly dark brown, partially subshiny; presutural supra-alar seta lacking or indistinguishable from surrounding setae. Wing hyaline, lacking any pattern or markings; costal vein ratio 0.74-0.79; M vein ratio 0.55-0.59. Legs, except tarsi, black; forefemur with posteroventral setae slender, not stout and peg-like; tarsi yellow; apical tarsomere slightly darker than other tarsomeres. Abdomen: Generally black, subshiny to mostly shiny, dorsum of tergites very sparsely and finely microtomentose, faintly whitish gray; sternite 3 of male rectangular, parallel sided, length twice width; sternite 4 of male rectangular, length almost twice width; sternite 5 of male a single, deeply U-shaped plate, length about twice width, opening of U posterior. Male terminalia (Figs 20-23): Epandrium in posterior view (Fig. 20) almost as wide as high, as an inverted U, dorsal arch very thin, verticolateral arms gradually becoming wider, width wider than width of cercus, in lateral view (Fig. 21) narrow, elongate, overall as a robust, irregular tear drop with an anteroventral, short, shallowly pointed projection; cercus in posterior view (Fig. 20) bar-like, elongate, narrow, with dorsal half wider than ventral half, slightly tapered from dorsum to ventral margin, not fused with ventral margin of cercal cavity, in lateral view (Fig. 21) elongate, dorsal half slightly wider than ventral half; gonite in ventral view (Fig. 22) as an inverted, robust comma, in lateral view (Fig. 23) bar-like, shallowly arched; aedeagus in lateral view (Fig. 23) robust, narrowly and irregularly rectangular, widest basally, thereafter slightly tapered to truncate apex, in ventral view (Fig. 22) elongate, narrow, narrowly ovate, acutely pointed apically; phallapodeme in lateral view (Fig. 23) as a deeply dissected triangle, extended keel rounded apically, each extended arm narrow, in ventral view (Fig. 22) narrow spindle shaped with a medial bulge, basal and apical widths subequal; hypandrium in ventral view (Fig. 22) as a robust V-shaped structure, vertex especially robust, in lateral view (Fig. 23) narrow, elongate, shallowly arched. + + + +Figures 18-19. +Lamproclasiopa triangularis +sp. n., male paratype (Peru. Madre de Dios: Manu) 18 head, anterior view 19 same, lateral view. Scale bar = 0.5 mm. + + + + +Figures 20-23. +Lamproclasiopa triangularis +sp. n., male paratype (Peru. Madre de Dios: Manu) 20 epandrium and cerci, posterior view 21 same, lateral view 22 internal structures of male terminalia (aedeagus [shaded], phallapodeme, gonite, hypandrium), ventral view 23 same, lateral view. Scale bar = 0.1 mm. + + + + + +Type +material. + + +The holotype male of +Lamproclasiopa triangularis +is labeled "PERU. Madre de Dios: Manu, Rio Manu, 250 m[,] Pakitza, +12°7'S +, +70°58'W +[ +11°56.6'S +, +71°16.9'W +], 9-23 Sep 1988[,] Amnon Freidberg/ USNM ENT 00118309 [plastic bar code label]/HOLOTYPE ♂ +Lamproclasiopa triangularis +Costa, Mathis & Marinoni, USNM [red]." The holotype is double mounted (minuten pin in a block of plastic), is in excellent condition, and is deposited in the USNM. Forty three paratypes (21♂, 22♀; DZUP, INPA, USNM) bear the same label data as the holotype but with W. N. Mathis as the collector. + + + +Type locality. + +Peru. Madre de Dios: +Rio +Manu, Pakitza ( +11°56.6'S +, +71°16.9'W +; 250 m). + + + + +Other +specimens examined. + + +BRAZIL. Amazonas: Manaus, Universidade Federal do Amazonas ( +03°05.9'S +, +59°58.2'W +; 50 m), 7 May 2010, D. and W. N. Mathis (3♂, 6♀; INPA, USNM). +Parana +: Antonina, Reserva Natural Rio Cachoeira ( +25°19'S +, +48°41,6'W +), 8 Feb 2010, D. Negoseki (1♂; DZUP). +Sao +Paulo: Ubatuba, Cachoeira da Lage ( +23°17.6'S +, +44°52.1'W +; 100 m), 30 Mar 2010, D. and W. N. Mathis (1♂, 3♀; DZUP, USNM). + + +ECUADOR. Orellana: Rio Tiputini ( +0°38.2'S +, +76°8.9'W +), 12-26 Aug 1999, W. N. Mathis, A. Batista, M. Kotrba (7♂, 2♀; USNM). + + +GUYANA. Kaieteur Falls ( +5°10.7'N +, +59°29.2'W +; 570 m), 7 Apr 1994, W. N. Mathis (1♂, 2♀; USNM). Kanuku Mountains, Kumu River and Falls ( +3°15.9'N +, +59°43.5'W +), 28-30 Apr 1995, W. N. Mathis (1♂; USNM). Kanuku Mountains, Moco Moco River ( +3°18.2'N +, +59°38.9'W +), 29 Apr 1995, W. N. Mathis (2♂, 1♀; USNM). Lethem (25 km SE; +3°18.2'N +, +59°38.9'W +), 4-5 Apr 1994, W. N. Mathis (2♂; USNM). + + +PERU. Madre de Dios: +Rio +Manu, Pakitza ( +11°56.6'S +, +71°16.9'W +; 250 m), 9-23 Sep 1988, A. Freidberg, W. N. Mathis (21♂, 23♀; USNM). + + + +Distribution + +(Fig. 81). Neotropical: Brazil (Amazonas, +Parana +, +Sao +Paulo), Ecuador (Orellana), Guyana, Peru (Madre de Dios). + + + +Etymology. + +The species epithet, +triangularis +, is of Latin derivation, meaning triangular, and refers to the small triangular microtomentose area on the face of this species. + + + +Remarks. +This species is distinguished from congeners by the triangle-shaped facial spot that is sparsely microtomentose. The triangle is situated medially on the ventral half of the face and is sometimes slightly elongated. Also distinguishing this species are the robust (thick) aedeagus in lateral view with its truncate apex and the narrow and elongated keel of the phallapodeme. + + + \ No newline at end of file diff --git a/data/38/CA/70/38CA7035087CA276900ADDC87BC6ED0C.xml b/data/38/CA/70/38CA7035087CA276900ADDC87BC6ED0C.xml new file mode 100644 index 00000000000..a998c1954de --- /dev/null +++ b/data/38/CA/70/38CA7035087CA276900ADDC87BC6ED0C.xml @@ -0,0 +1,49 @@ + + + +Description de nouveaux formicides éthiopiens (IIIme partie). + + + +Author + +Santschi, F. + +text + + +Revue de Zoologie Africaine + + +1926 + +13 + + +207 +267 + + + + +http://antbase.org/ants/publications/3617/3617.pdf + +journal article +3617 + + + + +Camponotus (Myrmosericus) vestitus Sm. v. comptus +n. var. + + + + +[[ queen ]]. Long: 12 mm. Rouge, gastre noir. Moitie anterieure de la tete, jaune roussatre. Antennes, pattes, une tache allongee sur les cotes du gastre d'un brun rougeatre. Pubescence comme chez +vestitus +type. Tete plus longue que chez ce type, un peu plus large derriere avec les cotes droits. Le scape ne la depasse que d'un quart de sa longueur. (D'un bon tiers chez le type) Yeux un peu plus petits que leur distance au bord posterieur de la tete. Pronotum un peu moins haut devant. Du reste comme chez le type mais plus robuste. Tete longue de 2,5 mm, large 2 mm. Cote d'Ivoire: Dimbroko, (Le Moult) 8 [[ queen ]]. + + + + \ No newline at end of file diff --git a/data/38/CA/E0/38CAE01438CCDFB4A75C5575D7ACBF08.xml b/data/38/CA/E0/38CAE01438CCDFB4A75C5575D7ACBF08.xml new file mode 100644 index 00000000000..d4f16c44dcc --- /dev/null +++ b/data/38/CA/E0/38CAE01438CCDFB4A75C5575D7ACBF08.xml @@ -0,0 +1,88 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part H) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +557 +585 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Hieracium paniculatum +Linnaeus + +, + +Species Plantarum +2 + +: 802. 1753 + + +. + + + +"Habitat in Canada. Kalm." RCN: 5862. + + + + +Lectotype +(Reveal in Jarvis & Turland in +Taxon +47: 362. 1998): +Kalm +, Herb. Linn. No. 954.20 ( +LINN +) + +. + + + + +Current name: + +Hieracium paniculatum +L. + +( +Asteraceae +). + + + + \ No newline at end of file diff --git a/data/38/CB/8F/38CB8F76E9E928CEF513CFB57B037EF4.xml b/data/38/CB/8F/38CB8F76E9E928CEF513CFB57B037EF4.xml new file mode 100644 index 00000000000..1a412359bc9 --- /dev/null +++ b/data/38/CB/8F/38CB8F76E9E928CEF513CFB57B037EF4.xml @@ -0,0 +1,80 @@ + + + +A biodiversity hotspot for Microgastrinae (Hymenoptera, Braconidae) in North America: annotated species checklist for Ottawa, Canada + + + +Author + +Fernandez-Triana, Jose + + + +Author + +Boudreault, Caroline + + + +Author + +Buffam, Joel + + + +Author + +Mclean, Ronald + +text + + +ZooKeys + + +2016 + +633 + + +1 +93 + + + + +http://dx.doi.org/10.3897/zookeys.63.10480 + +journal article +http://dx.doi.org/10.3897/zookeys.63.10480 +1313-2970-633-1 +DEFC153072414BA6B778CA63DB45B422 + + + +Taxon classification Animalia Hymenoptera Braconidae + + + +Dolichogenidea thujae (Muesebeck, 1935) +Fig. 24 + + + +Distribution. +NEA. + + +Material examined. +Ontario, Fallowfield, 45.267410 -75.829929, 18.vii.1960, C.D. Miller, Voucher Code: CNC475222; 19.vii.1960, C.D. Miller, Voucher Code: CNCHYM01157; 45.267531 -75.829886, 28.vii.1960, C.D. Miller, Voucher Code: CNC280957; Lanark, 45.018287 -76.365297, 27.vi.1951, Voucher Code: CNCHYM01159; 45.018354 -76.365257, 26.vi.1951, F.I.S., Voucher Code: CNC475224; 27.vi.1951, F.I.S., Voucher Code: CNC475223; Quebec, Aylmer, 45.395345 -75.844876, 14.vii.1960, C.D. Miller, Voucher Code: CNC475220; 15.vii.1960, C.D. Miller, Voucher Code: CNC475219; 18.vii.1960, C.D. Miller, Voucher Code: CNC475221; 45.4 -75.85, 19.vii.1960, Voucher Code: CNCHYM01158. + + +Figure 24. +Dolichogenidea thujae +. A Habitus, lateral B Head, frontal C Wings D Ovipositor sheaths and ovipositor E Metasoma, dorsal F Head and mesosoma, dorsal. + + + + + \ No newline at end of file diff --git a/data/38/CB/DF/38CBDFBFEF802EAFC8B8398F566B1D24.xml b/data/38/CB/DF/38CBDFBFEF802EAFC8B8398F566B1D24.xml new file mode 100644 index 00000000000..3dbecb61338 --- /dev/null +++ b/data/38/CB/DF/38CBDFBFEF802EAFC8B8398F566B1D24.xml @@ -0,0 +1,193 @@ + + + +Order Chiroptera - Family Vespertilionidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +451 +529 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Eptesicus (Eptesicus) furinalis +d'Orbigny 1847 + + + + + + + +Eptesicus (Eptesicus) furinalis +d'Orbigny 1847 + +, +Voy. Am. Merid., Atlas Zool., Vol. 4: 13 + +. + + + + +Type Locality: + +Argentina +, +Corrientes +. + + + + + +Vernacular Names: +Argentinian Brown Bat +. + + + + +Subspecies: +: + + +Subspecies + +Eptesicus (Eptesicus) furinalis +subsp. +furinalis +d'Orbigny 1847 + + + +Subspecies + +Eptesicus (Eptesicus) furinalis +subsp. +carteri +Davis 1965 + + + +Subspecies + +Eptesicus (Eptesicus) furinalis +subsp. +findleyi +Williams 1978 + + + +Subspecies + +Eptesicus (Eptesicus) furinalis +subsp. +gaumeri +J. A. Allen 1897 + + + + + +Distribution: +N +Argentina +, +Paraguay +, +Bolivia +, +Brazil +, and the Guianas east to +Peru +and north to +Jalisco +and +Tamaulipas +( +Mexico +). + + + + +Conservation: +IUCN +2003 and +IUCN +/ +SSC +Action Plan (2001) – Lower Risk (lc). + + + + +Discussion: +Subgenus + +Eptesicus + +. Reviewed by + +Williams (1978 +c +) + +. Apparently includes +dorianus +, but questions still remain about identity of the +holotype +; see + +Williams (1978 +c +) + +. Does not include + +chiralensis + +and + +montosus + +; see +Simmons and Voss (1998) +. + + + + \ No newline at end of file diff --git a/data/38/CC/37/38CC37BAE7111695A48BC1C8F3D72906.xml b/data/38/CC/37/38CC37BAE7111695A48BC1C8F3D72906.xml new file mode 100644 index 00000000000..6f4b47a0d4d --- /dev/null +++ b/data/38/CC/37/38CC37BAE7111695A48BC1C8F3D72906.xml @@ -0,0 +1,103 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part I) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +586 +598 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Iberis rotundifolia +Linnaeus + +, + +Species Plantarum +2 + +: 649. 1753 + + +. + + + +"Habitat in Helvetia." RCN: 4719. + + +Type not designated. + + + +Original material: + +Herb. Linn. No. 827.7? ( +LINN +) + +; [icon] in Barrelier, Pl. Galliam: 38, t. 848. 1714. + + + + +Current name: + + +Thlaspi cepaeifolium + +(Wulfen) W.D.J. Koch subsp. + +rotundifolium + +Greuter & Burdet + +( +Brassicaceae +). + + + + +Note: +Polatschek (in +Ann. Naturhist. Mus. Wien +70: 32. 1967) treated 827.4 (LINN) as +lectotype +, but this is an Allioni collection received by Linnaeus only in 1757, so it could not have been original material for the name. + + + + \ No newline at end of file diff --git a/data/38/CC/4A/38CC4AC438FBD28B45EA65E8F03453DA.xml b/data/38/CC/4A/38CC4AC438FBD28B45EA65E8F03453DA.xml new file mode 100644 index 00000000000..8d5e6949d0c --- /dev/null +++ b/data/38/CC/4A/38CC4AC438FBD28B45EA65E8F03453DA.xml @@ -0,0 +1,114 @@ + + + +Order Carnivora + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +532 +628 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Felis silvestris +subsp. +caudata +Gray 1874 + + + + + +Synonyms: + +Felis silvestris +subsp. +griseoflava +Zukowsky 1915 + +; + +Felis silvestris +subsp. +issikulensis +Ognev 1930 + +; + +Felis silvestris +subsp. +kozlovi +Satunin 1905 + +; + +Felis silvestris +subsp. +longipilis +Zukowsky 1915 + +; + +Felis silvestris +subsp. +macrothrix +Zukowsky 1915 + +; + +Felis silvestris +subsp. +matschiei +Zukowsky 1914 + +; + +Felis silvestris +subsp. +murgabensis +Zukowsky 1915 + +; + +Felis silvestris +subsp. +schnitnikovi +Birula 1915 + +. + + + + \ No newline at end of file diff --git a/data/38/CC/62/38CC62F91A7BD25BE65EB818E35286D2.xml b/data/38/CC/62/38CC62F91A7BD25BE65EB818E35286D2.xml new file mode 100644 index 00000000000..09f85497543 --- /dev/null +++ b/data/38/CC/62/38CC62F91A7BD25BE65EB818E35286D2.xml @@ -0,0 +1,127 @@ + + + +Flora der Schweiz und angrenzender Gebiete. Band 1. Pteridophyta bis Caryophyllaceae (2 nd edition): Registerzuband 1 + + + +Author + +Hess, Hans Ernst + + + +Author + +Landolt, Elias + + + +Author + +Hirzel, Rosmarie + +text + +1972 +Birkhaeuser Verlag + + +https://doi.org/10.5281/zenodo.291815 + +book +291815 +10.5281/zenodo.291815 +3-7643-0843-5 + + + +<subSubSection id="C7A7E361E5D6734A03E07D9089705D8D" pageId="null" pageNumber="380" type="nomenclature"> +<paragraph id="2C225C9B5E3A16C21623673A9EB30A52" pageId="null" pageNumber="380"> +<taxonomicName id="593474172385837144A3C17CE23350F7" ID-CoL="4W83N" ID-ENA="4550" authority="L." class="Liliopsida" family="Poaceae" genus="Secale" kingdom="Plantae" order="Poales" pageId="null" pageNumber="380" phylum="Tracheophyta" rank="species" species="cereale"> +<pageBreakToken id="3E98BCF3DF1B9B7664310931C2CD39CF" pageId="null" pageNumber="380">Secale</pageBreakToken> +<normalizedToken id="7B7D0EF7B6251C5C43C76A6682DD0E58" originalValue="cereále" pageId="null" pageNumber="380">cereale</normalizedToken> +L. +</taxonomicName> +</paragraph> +</subSubSection> +<subSubSection id="FB47751BE5EF476F2BBEABF2CA1B2147" pageId="null" pageNumber="380" type="vernacular_names"> +<paragraph id="C7B518AC697A0668820201DC75B15DFD" pageId="null" pageNumber="380">Saat-Roggen</paragraph> +</subSubSection> + + + +Aussaat meist im Herbst (Winterroggen), seltener im +Fruehjahr +(Sommerroggen). Pflanzen 0,8-2 m hoch. +Blaetter +blaugruen +, sonst wie bei + +Triticum + +(S.380); +Blatthaeutchen +kurz, gestutzt; +Blattoehrchen +klein, +kahl. +Aehre +5-20 cm lang, dicht, zur Reifezeit nickend. Die beiden +Blueten +in jedem +Aehrchen +nahe beisammen, selten 3 +Blueten +. +Huellspelzen +in eine kurze Granne +verschmaelert +oder spitz. - +Bluete +: +Frueher +Sommer. + + +Zytologische Angaben. +Siehe unter Gattung. + + +Standort. +Kollin, montan, im Wallis (Findelen) bis +gegen +2200 m. Weniger anspruchsvolle Getreideart als Weizen. + + + +Verbreitung +. +Urspruenglich +suedwestasiatische +Pflanze: + +Anbau begann bei uns +spaeter +als der von Weizen und Gerste, wahrscheinlich etwa zur Zeit Karls des +Grossen +im 8. Jh. In der Gegend von Wien soll nach Janchen (1963) schon vor 4500 Jahren Roggen angebaut worden sein. + + + +Bemerkungen. +S. montanum Guss. + +, verbreitet im Mediterrangebiet und +ostwaerts +bis Zentralasien, wird nach zytologischen Befunden als +Stammart +von + +S. cereale + +angesehen (Khush und Stebbins 1961). + + + + \ No newline at end of file diff --git a/data/38/CC/72/38CC72907981DE48EE99020239A73EA8.xml b/data/38/CC/72/38CC72907981DE48EE99020239A73EA8.xml new file mode 100644 index 00000000000..5f94fa4028f --- /dev/null +++ b/data/38/CC/72/38CC72907981DE48EE99020239A73EA8.xml @@ -0,0 +1,61 @@ + + + +Pheidole in the New World. A dominant, hyperdiverse ant genus. + + + +Author + +Wilson, E. O. + +text + +2003 +Harvard University Press + +Cambridge, MA + + + +http://atbi.biosci.ohio-state.edu/HymOnline/reference-full.html?id=20017 + +book +20017 + + + + +Pheidole harrisonfordi +new species + +Types Mus. Comp. Zool. Harvard. + + + +Etymology Named in honor of Harrison Ford, in recognition of his outstanding contribution in service and support to tropical conservation, hence the habitats in which the +Pheidole +ants will continue to exist. + + + + +diagnosis A small light-colored member of the +flavens +group similar to the species listed in the heading above, distinguished in the major by the bulbous pronotum in dorsal-oblique view, set off from a small but distinct mesonotal convexity, and the cephalic rugoreticulum, which starts as a patch at each occiput corner and runs anteriorly in a thin band to a patch just mesad to the eye. The minor is distinctive in the steep, nearly vertical descent of the posterior mesonotal face to the metanotum. + + + +Measurements (mm) Holotype major: HW 0.70, HL 0.80, SL 0.40, EL 0.08, PW 0.36. Paratype minor: HW 0.40, HL 0.44, SL 0.34, EL 0.06, PW 0.26. Color Major: body light reddish brown, appendages dark yellow. Minor: concolorous light reddish yellow. + + +Range Known from the type locality, and from Belmopan, Belize (Stewart B. and Jarmila Kukalova-Peck). + + +Biology The type series was collected on a steep, rocky forested slope (W. L. Brown); the Belize ants were taken from the ground in a Cecropia-palm forest. + + +figure Upper: holotype, major. Lower: paratype, minor. HONDURAS: El Sauce, Santa Barbara, 700 m (William L. Brown). Scale bars = 1 mm. + + + \ No newline at end of file diff --git a/data/38/CC/82/38CC82C6D66F9DBDD2ADA7BBEE5B555B.xml b/data/38/CC/82/38CC82C6D66F9DBDD2ADA7BBEE5B555B.xml new file mode 100644 index 00000000000..cb3fe27de5e --- /dev/null +++ b/data/38/CC/82/38CC82C6D66F9DBDD2ADA7BBEE5B555B.xml @@ -0,0 +1,53 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828--9042 + + + + +Gelis albopilosus Schwarz, 2002 + + + +Distribution +England + + +Notes + +added by +Schwarz (2002) + + + + \ No newline at end of file diff --git a/data/38/CC/9F/38CC9FE4608DD07573A7E32EB30523B6.xml b/data/38/CC/9F/38CC9FE4608DD07573A7E32EB30523B6.xml new file mode 100644 index 00000000000..b171744f782 --- /dev/null +++ b/data/38/CC/9F/38CC9FE4608DD07573A7E32EB30523B6.xml @@ -0,0 +1,84 @@ + + + +Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea + + + +Author + +Dale-Skey, Natalie + + + +Author + +Askew, Richard R. + + + +Author + +Noyes, John S. + + + +Author + +Livermore, Laurence + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8013 +8013 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8013 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8013 +1314-2828-4-8013 + + + + +Erythromalus nubilipennis (Walker, 1835) + + + + +Pteromalus nubilipennis +Walker, 1835 + + +Erythromalus nubilipennis +? +faustina +(Walker, 1839, +Pteromalus +) + + + +Distribution +England + + + \ No newline at end of file diff --git a/data/38/CC/FF/38CCFFDB3B5616D6ECC7F3C0278A36D7.xml b/data/38/CC/FF/38CCFFDB3B5616D6ECC7F3C0278A36D7.xml new file mode 100644 index 00000000000..4a7bee86496 --- /dev/null +++ b/data/38/CC/FF/38CCFFDB3B5616D6ECC7F3C0278A36D7.xml @@ -0,0 +1,78 @@ + + + +Chenopodiaceae + + + +Author + +Kuehn, U. + +text + + +1993 +Springer-Verlag + +Berlin, Heidelberg + + + + +Editor + +Kubitzki, K. + + + +Editor + +Rohwer, J. G. + + + +Editor + +Bittrich, V. + + +The Families and Genera of Vascular Plants 2 + + + +253 +281 + + + + +http://un.availab.le + +book chapter +3540555099 + + + + +19. +Suckleva A. Grav + + + + + + + +Suckleya A. Gray +, Proc. Amer. Acad. Arts 11: 103 (1876) + + + + + + +Annual, succulent herb, monoecious. Flowers in clusters, the staminate ones at the end of the branches; perianth 3-4 lobed, almost globose, lobes unequal; stamens 3-4; pistillate flowers axillary, 2-bracteolate; bracteoles folded, or keeled, later winged, often connate up to the middle; stigmas 2. Pericarp free from the globose seeds; embryo horseshoe-shaped; radicle pointing upward. One sp., S.suckleana (Torr.) Rydb., USA, Rocky Mountains, Montana to Colorado. + + + \ No newline at end of file diff --git a/data/38/CD/0A/38CD0A572CF3516EAE494A60B0331D0B.xml b/data/38/CD/0A/38CD0A572CF3516EAE494A60B0331D0B.xml new file mode 100644 index 00000000000..5936f422948 --- /dev/null +++ b/data/38/CD/0A/38CD0A572CF3516EAE494A60B0331D0B.xml @@ -0,0 +1,167 @@ + + + +Notes on the genus Ophryosporus (Asteraceae, Eupatorieae) in Chile + + + +Author + +Merklinger, Felix F. +University of Bonn, Nees Institute for Biodiversity of Plants, Meckenheimer Allee 170, D- 53115 Bonn, Germany +https://orcid.org/0000-0003-2197-0412 +felixfranz.merklinger@zuerich.ch + + + +Author + +Luebert, Federico +University of Bonn, Nees Institute for Biodiversity of Plants, Meckenheimer Allee 170, D- 53115 Bonn, Germany & Departmento de Silvicultura y Conservacion de la Naturaleza, Universidad de Chile, Av. Santa Rosa 11315, Santiago, Chile + +text + + +PhytoKeys + + +2020 + +161 + + +61 +77 + + + + +http://dx.doi.org/10.3897/phytokeys.161.53736 + +journal article +http://dx.doi.org/10.3897/phytokeys.161.53736 +1314-2003-161-61 +540913ADED1758EB839CD921EA0403FF + + + + +Ophryosporus anomalus R.M.King & H.Rob., Phytologia 25: 66. 1972 + + + + +Typonym: +Piqueria cumingii +B.L.Rob., Proc. Amer. Acad. Arts, 42: 11. 1906, non +Ophryosporus cumingii +Benth. ex Baker (1895: 188, based on +Mandon 264 +from Bolivia.). + + + +Type. + +Chile. Region I +Tarapaca +and Region II Antofagasta: "Peruvia meridionalis: Cobija, Iquiqui et Arica", +H.Cuming 953 +(lectotype, selected by +Plos and Sancho (2013 +: 338): K [K000486684, photo!]; isolectotypes E [E00322766, photo!], GH [GH00010778!], K [K000486685, photo!], P [P02673192, photo!]); remaining syntypes: +Gaudichaud +s.n. (B [probably destroyed, could not be found], F [F1012247, photo!]). + + + +Ophryosporus anomalus + +has been cited for Peru ( +King and Robinson 1972b +; +Brako and Zarucchi 1993 +), likely due to the type collection label ("Peruvia meridionalis..."). However, the localities mentioned there ("...Cobija, Iquiqui et Arica") are now situated in Chile, and all other reports originate from the coastal zone around Tocopilla ( +Johnston 1932 +; +Jaffuel 1936 +) and therefore +Luebert et al. (2007) +considered it a Chilean endemic. We hereby extend the distribution of the species to include the populations from the coastal area between +Rio +Loa and Iquique, previously referred to as + +O. floribundus + +( + +Munoz-Schick +et al. 2001 + +; +Pinto and Luebert 2009 +). See discussion below under the latter species. + + + +Specimens examined. + +Chile. Region I +Tarapaca +: Prov. Iquique, Alto Punta Gruesa, +20°22'S +, +70°09'W +, 14 Dec 1997, +R. Pinto s.n. +(SGO142948); Alto Punta Patache, +20°49'S +, +70°09'W +, 6 Dec 1997, +R. Pinto s.n. +(SGO142949); Alto Punta Patache, 22 Jan 2000, +R. Pinto s.n. +(SGO [photo]); Alto Punta Lobos, +21°02'S +, +70°09'W +, 14 Jan 1998, +R. Pinto s.n. +(SGO142950); Alto Chipana, +21°16'S +, +70°03'W +, 15 Oct 1997, +W. Sielfeld 7 +(SGO143038); Alto Chipana, +21.304528S +, +70.03204W +, 990 m, 21 Oct 2016, + +F. Luebert, A. Stoll & T. +Boehnert +3427A + +(BONN, ULS); Alto Chipana, +21.292633S +, +70.042234W +, 840 m, 1 Oct 2019, +F. Luebert, F.F. Merklinger & J. Ruhm 4102 +(BONN, EIF, K). Region II Antofagasta: Prov. Tocopilla, Tocopilla, 27 Oct 1930, +F. Jaffuel 1026 +(GH); Tocopilla, Cerro Rosario, 1 Nov 1941, +M.R. Espinosa s.n. +(SGO143254); Cobija, s.a., +C. Gaudichaud s.n +. (F1012247); Cobija, quebrada Aguada +Canas +, 4 Apr 1949, +W. Biese 3088 +(SGO096693). + + + + \ No newline at end of file diff --git a/data/38/CD/12/38CD12EF2EBC742D74CEF1CD717088F8.xml b/data/38/CD/12/38CD12EF2EBC742D74CEF1CD717088F8.xml new file mode 100644 index 00000000000..3307d4c618b --- /dev/null +++ b/data/38/CD/12/38CD12EF2EBC742D74CEF1CD717088F8.xml @@ -0,0 +1,92 @@ + + + +Checklist of Serengeti Ecosystem Grasses + + + +Author + +Williams, Emma Victoria + + + +Author + +Elia Ntandu, John + + + +Author + +Ficinski, Pawel + + + +Author + +Vorontsova, Maria + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8286 +8286 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8286 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8286 +1314-2828--8286 + + + + +Dichanthium annulatum var. annulatum + + + +Materials + + +Type status: +Other material +. Occurrence: catalogNumber: +1147 +; recordNumber: 819B; recordedBy: +Mollel, NP; Rusch, GM; Mwakalebe, G +; Taxon: scientificName: Dichanthiumannulatum(Forssk.)Stapfvar.annulatum; kingdom: Plantae; family: Poaceae; genus: Dichanthium; specificEpithet: annulatum; infraspecificEpithet: annulatum; scientificNameAuthorship: (Forssk.) Stapf; Location: continent: Africa; country: +Tanzania +; stateProvince: Mara; county: Serengeti; locality: +Robanda village +; verbatimLocality: Robanda village, road to the water pool, CG01 plot 36M, 0386088, 9763754 UTM.; minimumElevationInMeters: 1388; decimalLatitude: +-2.083333 +; decimalLongitude: +34.666667 +; Event: eventDate: +2003-01-28 +; Record Level: institutionCode: +NHT +; collectionCode: +Herbarium +; ownerInstitutionCode: NHT; basisOfRecord: PreservedSpecimen + + + + +Distribution +Widespread + + + \ No newline at end of file diff --git a/data/38/CD/7D/38CD7D7F69B481CDDDF0BEFF7364CC75.xml b/data/38/CD/7D/38CD7D7F69B481CDDDF0BEFF7364CC75.xml new file mode 100644 index 00000000000..7c2287c0d9a --- /dev/null +++ b/data/38/CD/7D/38CD7D7F69B481CDDDF0BEFF7364CC75.xml @@ -0,0 +1,115 @@ + + + +Family-group names in Coleoptera (Insecta) + + + +Author + +Bouchard, Patrice + + + +Author + +Bousquet, Yves + + + +Author + +Davies, Anthony E. + + + +Author + +Alonso-Zarazaga, Miguel A. + + + +Author + +Lawrence, John F. + + + +Author + +Lyal, Chris H. C. + + + +Author + +Newton, Alfred F. + + + +Author + +Reid, Chris A. M. + + + +Author + +Schmitt, Michael + + + +Author + +Ślipinski, S. Adam + + + +Author + +Smith, Andrew B. T. + +text + + +ZooKeys + + +2011 + +88 + + +1 +972 + + + + +http://dx.doi.org/10.3897/zookeys.88.807 + +journal article +http://dx.doi.org/10.3897/zookeys.88.807 +1313-2970-88-1 + + + + +Subfamily +Eumolpinae Hope, 1840 + + + + +Eumolpidae +Hope, 1840a: 162 [stem: Eumolp-]. Type genus: +Eumolpus +Kugelann, 1798 [an application to suppress +Eumolpus +Kugelann, 1798 and conserve +Eumolpus +Weber, 1801 was recently submitted to the Commission by Moseyko et al. (2010)]. + + + + \ No newline at end of file diff --git a/data/38/CD/FD/38CDFD0A2BCC529BBD39F39BA0032BFA.xml b/data/38/CD/FD/38CDFD0A2BCC529BBD39F39BA0032BFA.xml new file mode 100644 index 00000000000..968552710ea --- /dev/null +++ b/data/38/CD/FD/38CDFD0A2BCC529BBD39F39BA0032BFA.xml @@ -0,0 +1,285 @@ + + + +Ecotone shifts in southern Madagascar: first barcoding data and six new species of the endemic millipede genus Riotintobolus (Spirobolida, Pachybolidae) + + + +Author + +Wesener, Thomas +Zoological Research Museum Alexander Koenig (ZFMK), Leibniz Institute for Animal Biodiversity, Adenauerallee 160, D- 53113, Bonn, Germany +t.wesener@leibniz-zfmk.de + +text + + +ZooKeys + + +2020 + +953 + + +1 +29 + + + + +http://dx.doi.org/10.3897/zookeys.953.53977 + +journal article +http://dx.doi.org/10.3897/zookeys.953.53977 +1313-2970-953-1 +BA81E87988A2495A92FB98D1F2909BA7 +C7001D577310538DBE2A4736802E1BF4 + + + + +Riotintobolus lavanono +sp. nov. +Figure 7 + + + +Material examined. + +1 ♂ +holotype +, +ZFMK MYR9941 +, Madagascar, South, Lavanono Beach, +25°25.404'S +, +044°56.414'E +, 27 m, spiny bush at the coast, after rain, leg. Wesener and +Schuette +, 18.vi.2007. + + +Paratypes +: 16 ♂, 18 ♀, +ZFMK MYR942 +, same data as holotype; + + + +Etymology. + +Lavanono, after the type locality, spiny forests directly next to the Lavanono Beach (Fig. +2 +). Noun in apposition. + + + +Diagnosis. + + +Riotintobolus lavanono + +sp. nov. shares the absence of a projecting epiproct on the telson with + +R. anomalus + +, + +R. antafoky + +sp. nov., + +R. bovinus + +sp. nov., + +R. tsimelahy + +sp. nov. and + +R. mangatsiaka + +sp. nov., The posterior telopod featuring two slender, sharp projections is only shared with + +R. bovinus + +sp. nov., + +R. mangatsiaka + +sp. nov. and + +R. tsimelahy + +sp. nov. A posterior gonopod separated into three parts is only shared with + +R. mangatsiaka + +sp. nov. and + +R. tsimelahy + +sp. nov., whose habitus and gonopods look very similar to those of + +R. lavanono + +sp. nov. Both species differ in details of the tip of the posterior gonopod and in the colour of their antennae and legs, which are dark grey in + +R. lavanono + +sp. nov. and red in both + +R. mangatsiaka + +sp. nov. and + +R. tsimelahy + +sp. nov. All three species differ by>11% uncorrected p-distance in the COI barcoding gene. + + + +Description. + +Measurements +: male holotype with 47+0 segments, ca. 42 mm long, 4.2 mm wide. Largest females of type series with 46-48+0 segments, up to 58 mm long, 6.4 mm wide. + + +Colour +(in living specimens): Body rings and head grey, appendages black (Fig. +7A +). Paraprocts and posterior margins of body segments darker grey to black (Fig. +7B +). Ozopore openings highlighted by black spot. + + + +Figure 7. + +Riotintobolus lavanono + +sp. nov., paratype male (ZFMK MYR942) +C +anterior gonopod, anterior view; posterior view +D +telopodite of left posterior gonopod, posterior view +E +left posterior gonopod, anterior view. +Abbreviations +: av = paraprocts; Co = collum (ring 1); Cx = coxite; Go = gonopods; Md = basal joints of mandible; Pre = epiproct; St = sternite; sub = hypoproct; T = telopodite; x = lateral swollen process; y = opening of efferent duct; z = apical membranous +'flag' +; numbers refer to leg pair or segment number. Scale bars: 1 mm. + + + +Head +: each eye with 28-32 ommatidia in six rows. Incisura lateralis open (Fig. +7A +). Labrum with standard three irregular teeth and a single row of 10-12 stout marginal setae. Clypeus with two setiferous foveolae on each side. Antennae long, protruding back to segment 5. Length of antennomeres: 1<2>3>4=5=6. Terminal antennomere with four large sensory cones located together inside a membranous area. Antennomere 5 and 6 latero-apically with sensilla basiconica. + + +Gnathochilarium +: lamellae linguales each with two standard setae located behind one another. Stipites each with three apical setae. Endochilarium not dissected. + + +Mandible +: Stipes without projection, well rounded (Fig. +7A +). Gnathal lobe not investigated. + + +Collum +: smooth, laterally not protruding as far as ring 2 (Fig. +7A +). + + +Body rings +: ozopores starting at segment 6, marked by a black spot. Located on suture between meso- and metazonite. Rings with smooth, but irregular coriaceous surface, ventrally on metazona with transverse ridges. + + +Telson +: paraprocts elongated, with weak lips, abundant micropunctation especially towards edges (Fig. +7B +). Epiproct well-rounded, covering, but not reaching above paraproct (Fig. +7B +). Hypoproct inconspicuous (Fig. +7B +). + + +Legs +: leg 1 with a large cylindrical coxa, twice as long as other podomeres. Tarsus with three pairs of ventral spines and an apical spine beyond claw. Leg 2 with an elongated coxa. Tarsus with three pairs of ventral spines and a short apical spine. Midbody legs with a rectangular coxa, as long as other podomeres. Each podomere ventrally with a single or a pair of apical setae, tarsus with a single apical and four pairs of ventral spines. Length of midbody legs ca. 1.2 times body diameter in males. + + + +Female sexual characters +. + +No tarsal pads, antennae shorter than male, only protruding back to ring 2. Female vulva simple, bivalve-like. + + +Male sexual characters +: tarsal pads present from leg 3 to midbody, small, inconspicuous. Coxae 3-7 without coxal processes, but coxae 3-5 swollen. + + +Anterior gonopod +sternite massive, elongated into a wide, well-rounded triangular lobe (Fig. +7C +). Sternite in anterior view well-visible, without discernible apodemes, protruding almost as high as coxal processes. Coxite with a large, well-rounded mesal process. Telopodite with slender process arising mesally (Fig. +7C +), process apically curved with a large triangular projection, tip well-rounded, slightly protruding above lateral margin of telopodite. + + +Posterior gonopods +consisting of three parts, separated by sutures or articulations (Fig. +7D +): a basal coxite with a slender coxite projection and a shorter telopodite, efferenct duct discharging laterally (Fig. +7E +). Process of coxite and telopodite standing in same axis. Pair of posterior gonopods located parallel to each other, connected by a small, sclerotised and visible sternite. Basal part of coxite wide, mesally with a large triangular sclerite located on lower level than remaining part. Coxite elongated. Efferent duct running at mesal margin of coxite before curving to the lateral margin at beginning of telopodite (Fig. +7E +). Telopodite half as wide and much shorter than coxite, standing in same axis, apically membranous, with two slender apical processes both diverging (Fig. +7D, E +). Mesal process membranous and wider, lateral process bent 90 degrees laterally, longer, slenderer and sclerotised, efferent duct seems to be ending at base of lateral process (Fig. +7E +). Base of lateral process with a short, membranous-white projection (Fig. +7E +). + + + +Intraspecific variation. +Specimens of the same population differing between 45-47 in segment number. Females appear to be more brownish than the more greyish males. + + +Live observations. + + +R. lavanono + +sp. nov. could be found in great numbers after a rainy day in the late afternoon (3-5 p.m.) in a small remnant of spiny bush and under dead + +Opuntia + +remains. The specimens were only encountered in an area of a few square meters in view of the coast. Contrary to other + +Riotintobolus + +species, such as + +R. mandenensis + +and + +R. minutus + +, + +R. lavanono + +sp. nov. did not remain stiff like a stick when disturbed, but rolled-up into a spiral. + + + + \ No newline at end of file diff --git a/data/38/CE/13/38CE137F4E9057BD5933AFBC893E6C66.xml b/data/38/CE/13/38CE137F4E9057BD5933AFBC893E6C66.xml new file mode 100644 index 00000000000..82a3a1ff60a --- /dev/null +++ b/data/38/CE/13/38CE137F4E9057BD5933AFBC893E6C66.xml @@ -0,0 +1,74 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828-4-9042 + + + + +Campoplex tumidulus Gravenhorst, 1829 + + + + +ensator +misident. + + +nigrifemur +(Seyrig, 1928, +Omorgus +) + + +rufinator +Aubert, 1971 + + + +Distribution +England, Scotland, Wales, Ireland, Isle of Man + + +Notes + +Recorded as +Campoplex rufinator +by +Shaw (1984) +and +Shaw and Aeschliman (1994) +. + + + + \ No newline at end of file diff --git a/data/38/CE/83/38CE839A99A81BAD7714F143DDF22D50.xml b/data/38/CE/83/38CE839A99A81BAD7714F143DDF22D50.xml new file mode 100644 index 00000000000..202d5d33876 --- /dev/null +++ b/data/38/CE/83/38CE839A99A81BAD7714F143DDF22D50.xml @@ -0,0 +1,94 @@ + + + +Birds from the Azores: An updated list with some comments on species distribution + + + +Author + +Barcelos, Luis MD + + + +Author + +Rodrigues, Pedro R + + + +Author + +Bried, Joel + + + +Author + +Mendonca, Enesima P + + + +Author + +Gabriel, Rosalina + + + +Author + +Borges, Paulo Alexandre Vieira + +text + + +Biodiversity Data Journal + + +2015 + +3 + + +6604 +6604 + + + + +http://dx.doi.org/10.3897/BDJ.3.e6604 + +journal article +http://dx.doi.org/10.3897/BDJ.3.e6604 +1314-2828--6604 + + + + +Gallinula chloropus chloropus (Linnaeus, 1758) + + + +Ecological interactions + +Native status +Palearctic + + +Conservation status +A-IIB; AEWA + + + +Distribution +COR*; FLO (Breeder); FAI*; PIC*; GRA*; SJG*; TER (Breeder); SMG (Breeder); SMR (Breeder) + + +Notes + +Native. +Rodrigues et al. (2010) + + + + \ No newline at end of file diff --git a/data/38/CE/E0/38CEE09711B953099BB85889C0498A32.xml b/data/38/CE/E0/38CEE09711B953099BB85889C0498A32.xml new file mode 100644 index 00000000000..62610d8e2be --- /dev/null +++ b/data/38/CE/E0/38CEE09711B953099BB85889C0498A32.xml @@ -0,0 +1,152 @@ + + + +Integrative taxonomy of New World Euplectrus Westwood (Hymenoptera, Eulophidae), with focus on 55 new species from Area de Conservacion Guanacaste, northwestern Costa Rica + + + +Author + +Hansson, Christer + + + +Author + +Smith, M. Alex + + + +Author + +Janzen, Daniel H. + + + +Author + +Hallwachs, Winnie + +text + + +ZooKeys + + +2015 + +485 + + +1 +236 + + + + +http://dx.doi.org/10.3897/zookeys.485.9124 + +journal article +http://dx.doi.org/10.3897/zookeys.485.9124 +1313-2970-485-1 +F18CFD3D10294E8AA2E8CEF1AFDBAC8F +F18CFD3D10294E8AA2E8CEF1AFDBAC8F + + + +Taxon classification Animalia Hymenoptera Eulophidae + + + +Euplectrus markshawi Hansson +sp. n. +Figures 264-267, 271-273, 770 + + + +Material. + +Holotype a female labeled "COSTA RICA: Guanacaste, ACG, Sector Santa Rosa, Quebrada Costa Rica, 12.vi.2006, D. Rivera, ex +Cargida pyrrha +eating +Colubrina elliptica +, sibling of wasp DHJPAR0028896, 06-SRNP-16286" (BMNH). PARATYPES: 2♀ with same label data as holotype (BMNH, INBio). + + + +Diagnosis. + +Lower face with median part yellowish-brown, slightly darker medially, pale area reaching outside of outer lateral margins of toruli, with a black area the width of width of scape between pale area and eye margin (Fig. 265); scutellum with a small hump posteromedially and reticulate with elongate meshes, scutellum hence appearing striate (Fig. 273); dorsellum anteriorly with a wide groove, 0.5 +x +as long as length of dorsellum (Fig. 770); legs yellowish-brown with hind coxa pale brown (Fig. 257); petiole 0.6 +x +as long as wide; gaster with anterior +1/2 +yellowish-brown with dark brown lateral margins, posterior +1/2 +difficult to see on specimens because apical segments are retracted (Fig. 266). Very similar to +Euplectrus ivonae +, differs in having first tarsomere longer (LT/LT1 = 2.5; = 3.0 in +Euplectrus ivonae +), petiole shorter (LP/WP = 0.6; = 0.8 in +Euplectrus ivonae +), and with hind coxae darker. + + + +Description. + +Female +. Length of body 2.1 mm. Antenna with scape yellowish-white in basal +1/2 +, yellowish-brown in apical +1/2 +, pedicel yellowish-brown, flagellomeres 1-3 dark brown dorsally and yellowish-brown ventrally, 4-6 dark brown (Fig. 267). Mandibles and palpi yellowish-white. Head black and shiny, lower face with median part yellowish-brown, slightly darker medially, pale area reaching outside of outer lateral margins of toruli, with a black area the width of width of scape between pale area and eye margin (Fig. 265). Frons close to eyes with two rows of setae (Fig. 271). Vertex with very weak reticulation inside ocellar triangle, outside triangle smooth (Fig. 272). Occipital margin with a weak carina behind ocellar triangle (Fig. 272). + + +Mesosoma black and shiny (Fig. 264). Each sidelobe of mesoscutum with 14 setae. Scutellum 1.0 +x +as long as wide; with rather strong engraved reticulation, meshes elongate and scutellum appearing striate, in posteromedian +1/2 +with a small hump (Fig. 273). Dorsellum anteriorly with a wide groove that is divided by longitudinal carinae (Fig. 770), groove medially 0.5 +x +as long as length of dorsellum. Propodeum smooth (Fig. 770); anteromedially with a transverse semicircular cup; propodeal callus with seven setae. Legs yellowish-brown with hind coxa pale brown (Fig. 264). Fore wing: costal cell with one row of setae on ventral surface, and margin with two setae close to marginal vein; with 16 admarginal setae, in one row. + + +Gaster with anterior +1/2 +yellowish-brown with dark brown lateral margins, posterior +1/2 +difficult to see on specimens (Fig. 266). + +Ratios. HE/MS/WM = 1.8/1.0/1.1; POL/OOL/POO = 4.8/2.8/1.0; OOL/DO = 1.7; WE/WF/WH/HH = 1.0/2.5/4.3/3.5; WH/WT = 1.1; PM/ST = 1.4; TS1/TS2/LT/LT1/LT2/LT3/LT4 = 4.6/2.6/7.4/3.0/1.5/1.0/1.6; LP/WP = 0.6; MM/LG = not measurable, gaster with retracted apical segments. +Male. Unknown. + + +Hosts and biology. + +Feeding on last instar larva of +Cargida pyrrha +( +Notodontidae +) feeding on +Colubrina elliptica +( +Rhamnaceae +), parasitoid cocoons stuck to dead larva and substrate. + + + +Distribution. +Costa Rica (Guanacaste Province). + + +Etymology. + +This species is named after Mark R. Shaw, in recognition of his contribution to the understanding of ACG +Hymenoptera +taxonomy. + + + + \ No newline at end of file diff --git a/data/38/CF/52/38CF52C923D222C9CBC18016C6B68328.xml b/data/38/CF/52/38CF52C923D222C9CBC18016C6B68328.xml new file mode 100644 index 00000000000..d77589e96da --- /dev/null +++ b/data/38/CF/52/38CF52C923D222C9CBC18016C6B68328.xml @@ -0,0 +1,94 @@ + + + +Order Carnivora + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +532 +628 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Poiana richardsonii +subsp. +richardsonii +Thomson 1842 + + + + + + + +Poiana richardsonii +subsp. +richardsonii +Thomson 1842 + +, +Ann. Mag. Nat. Hist., ser. 1, 10: 204 + +. + + + + +Type Locality: + +" +Fernando Po +" [ +Equatorial Guinea +: Bioko]. + + + + + +Synonyms: + +Poiana richardsonii +subsp. +poensis +( +Waterhouse 1838 +) + +. + + + + \ No newline at end of file diff --git a/data/38/CF/EC/38CFEC3AFAF9D863215C6FA89C506AB6.xml b/data/38/CF/EC/38CFEC3AFAF9D863215C6FA89C506AB6.xml new file mode 100644 index 00000000000..216d6f2d5c3 --- /dev/null +++ b/data/38/CF/EC/38CFEC3AFAF9D863215C6FA89C506AB6.xml @@ -0,0 +1,52 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Aranea bipunctata +[ +spec. nov. +] + + + + +A. abdomine globoso atro: punctis duobus excavatis. +Fn. svec. +1232. + + + + +Habitat in +fenestris. +Rete disperso. + + + + \ No newline at end of file diff --git a/data/38/CF/F3/38CFF3183E7D5A4A9FF3856DCDFD0CBA.xml b/data/38/CF/F3/38CFF3183E7D5A4A9FF3856DCDFD0CBA.xml new file mode 100644 index 00000000000..fb40d34aeb8 --- /dev/null +++ b/data/38/CF/F3/38CFF3183E7D5A4A9FF3856DCDFD0CBA.xml @@ -0,0 +1,284 @@ + + + +Integrative taxonomy supports two new species of Chimarra Stephens, 1829 from Brazil (Trichoptera: Philopotamidae) + + + +Author + +Moreira, Paula Dias +https://orcid.org/0000-0003-4994-9121 +Laboratorio de Entomologia, Departamento de Zoologia, Instituto de Biologia, Universidade Federal do Rio de Janeiro, Caixa Postal 68044, Rio de Janeiro, 21941 - 970, RJ, Brazil +paulaentomobio@gmail.com + + + +Author + +Dumas, Leandro Lourenco +Laboratorio de Entomologia, Departamento de Zoologia, Instituto de Biologia, Universidade Federal do Rio de Janeiro, Caixa Postal 68044, Rio de Janeiro, 21941 - 970, RJ, Brazil & Departamento de Biologia Animal, Instituto de Ciencias Biologicas e da Saude, Universidade Federal Rural do Rio de Janeiro, Seropedica, RJ, Brazil + + + +Author + +Rozo, Maria Paula +Laboratorio de Entomologia, Departamento de Zoologia, Instituto de Biologia, Universidade Federal do Rio de Janeiro, Caixa Postal 68044, Rio de Janeiro, 21941 - 970, RJ, Brazil + + + +Author + +Desiderio, Gleison Robson +https://orcid.org/0000-0002-5048-9786 +Departamento de Biologia Animal, Instituto de Ciencias Biologicas e da Saude, Universidade Federal Rural do Rio de Janeiro, Seropedica, RJ, Brazil + + + +Author + +Takiya, Daniela Maeda +https://orcid.org/0000-0002-6233-3615 +Laboratorio de Entomologia, Departamento de Zoologia, Instituto de Biologia, Universidade Federal do Rio de Janeiro, Caixa Postal 68044, Rio de Janeiro, 21941 - 970, RJ, Brazil + +text + + +Arthropod Systematics & amp; Phylogeny + + +2022 + +2022-05-30 + + +80 + + +169 +185 + + + + +http://dx.doi.org/10.3897/asp.80.e76559 + +journal article +http://dx.doi.org/10.3897/asp.80.e76559 +1864-8312-80-169 +975D4BBF4D7B46449BF434EAE6074999 +490FF3AD3CD452FFA0994708CA25F3A6 + + + + + +3.2.2. +Chimarra (Otarrha) paraodonta +sp. nov. + + + +Type locality. + +Cachoeira +Veu +da Noiva, Parque Nacional do Itatiaia, Itatiaia, Rio de Janeiro State, Brazil. + + + +Diagnosis. + +The new species is closely similar to +C. (Otarrha) odonta +Blahnik, 2002 by some shared primitive characters of the subgenus, like hindwing venation pattern with Rs 4-branched and the undivided anterior head setal warts. Both species also have a simple, subtriangular, and completely divided tergum X and an inner process on each inferior appendage. However, the new species has the + +Otarrha + +synapomorphic hindwing venation with Sc+R1 fused, narrower and more uniform lobes of tergum X, and inferior appendage rhomboidal (in lateral view) and more elongated and spatulated (in ventral view). Additionally, the dorsomesal process of the inferior appendage in +C. (Otarrha) paraodonta +sp. nov. +is thorn-like, more robust, and positioned subapically; while in + +C. odonta + +, this process is tooth-like, blunt, and positioned more apically. Furthermore, +C. (Otarrha) paraodonta +sp. nov. +can be recognized by its differently shaped tergum IX as viewed dorsally, the more robust ventral process, and simple phallotremal sclerite. + + + +Description. + +Adult male +: forewing length 5.2-5.8 mm (n=3; holotype = 5.8 mm). General color (in alcohol) uniformly golden brown, except dark brown dorsum of head. Dorsum of head with anterior, anteromesal, posterior, and posterolateral setal warts; posterolateral setal warts large; anterior setal warts each elongate and undivided; postocular parietal sclerite large, slightly extending below the eye. Maxillary palps relatively short, 2nd segment shorter than 3rd segment, apicomesally with stout setae. Wing venation typical for the subgenus (Fig. +5A-B +), except Rs of hind wing 4-branched (Fig. +5B +); forewing with forks I, II, III, and V present, stem of Rs almost straight, crossveins +s +, +r-m +and +m +linearly arranged and unpigmented, crossveins +m-cu +and +cu +and apex of Cu2 also hyaline; 2A not forked (Fig. +5A +); hind wing with forks I, II and V present, R1 and Sc fused; crossveins +s +and +r-m +not aligned and unpigmented, crossvein +m-cu +apparently absent, +cu-a +present, anal loop very small (Fig. +5B +). Tibial spur formula 1-4-4. + + +Male genitalia +(Fig. +6 +): Segment IX, dorsally with anterior margin deeply concave, posterior margin almost straight (Fig. +6B +); in lateral view, with anterior margin almost straight, somewhat projected in the anteroventral portion; posterior margin sinuous, with distinct dorsomedial and ventromedial invagination (Fig. +6A +); ventral process elongate, about same length of inferior appendage as viewed laterally, enlarging apically with rounded apex (Fig. +6A +, +6C +). Tergum X, in dorsal view, completely divided mesally, forming elongate, paired narrow sclerotized lobes, slightly tapering apically; apex rounded (Fig. +6B +); each lobe with numerous apical and basoventral sensilla (Fig. +6A +, +6B +); in lateral view, subtriangular (Fig. +6A +). Preanal appendages flattened, earlike, laterally directed (Fig. +6A, B +). Inferior appendages, in lateral view, rhomboidal, relatively short (Fig. +6A +); each appendage with subapical thorn-like process on the dorsomesal surface (Fig. +6A, C, D +); in dorsal view, with outer lateral margin expanded distally (Fig. +6D +); in ventral view, spatulate, with truncate distal margin (Fig. +6B +). Phallic apparatus with phallotheca tubular, bearing basodorsal and basoventral pointed extensions; endotheca short, membranous, with 4 apical, robust, sclerotized spines; phallotremal sclerite simple, large, L-shaped (Fig. +6E, F +). + + + +Figure 5. +Chimarra (Otarrha) paraodonta +sp. nov. +, holotype wing venation: +A +right forewing; +B +right hind wing. Abbreviations: DC, discoidal cell; MC, medial cell; TC, thyridial cell. + + + + +Figure 6. +Chimarra (Otarrha) paraodonta +sp. nov. +, holotype male genitalia: +A +left lateral view; +B +dorsal view; +C +ventral view; +D +left inferior appendage, dorsal view; +E +phallus, left lateral view; +F +phallus, ventral view. + + + + +Etymology. + +The specific epithet is a reference to the close similarity of the new species to +Chimarra (Otarrha) odonta +. Derived from the Greek, " +para +" = beside or near. + + + +Material examined. +Holotype +. + +BRAZIL • ♂; Rio de Janeiro State, Itatiaia, Parque Nacional do Itatiaia, Complexo da Maromba, Cachoeira +Veu +da Noiva; + +22°25 +'38.6" +S + +, + +44°37 +'9.7" +W + +; el. 1140 m a.s.l.; 02-19.ii.2015; D.M. Takiya & A.P.M. Santos leg.; Malaise trap; DZRJ 7828 (DNA voucher ENT5579). - + +Paratypes +. + +BRAZIL • 1 ♂; Rio de Janeiro State, Itatiaia, Parque Nacional do Itatiaia, Complexo da Maromba, Cachoeira +Veu +da Noiva [PNI-M2A]; + +22°25 +'36.1" +S + +, + +44°37 +'05.80" +W + +; el. 1153 m a.s.l; 02.x-02.xi.2015; M.L. +Monne +, J.P. Botero, +A +.P. Pinto, L.H. Gil-Azevedo; Malaise trap, MNRJ (DNA voucher ENT5578) • 1 ♂; Rio de Janeiro State, Itatiaia, Parque Nacional do Itatiaia, abaixo da Cachoeira +Veu +da Noiva; + +22°25 +'36.10" +S + +, + +44°37 +'05.80" +W + +; el. 153 m a.s.l.; 02.x.2015; C.C.D. +Correa +& L.H. Gil-Azevedo leg.; INPA (DNA voucher ENT5577). + + + + + \ No newline at end of file diff --git a/data/38/D0/60/38D06000281B97629B0CEF07C96EB706.xml b/data/38/D0/60/38D06000281B97629B0CEF07C96EB706.xml new file mode 100644 index 00000000000..cf5897444ac --- /dev/null +++ b/data/38/D0/60/38D06000281B97629B0CEF07C96EB706.xml @@ -0,0 +1,194 @@ + + + +Flora Helvetica - Poaceae + + + +Author + +Konrad Lauber + + + +Author + +Gerhart Wagner + + + +Author + +Andreas Gygax + +text + + +2018 +Haupt Verlag + +Bern + + + +Flora Helvetica + + + +1458 +1570 + + + +book chapter +978-3-258-08047-5 + + + + + +Deschampsia cespitosa +(L.) P. Beauv. + + + + + +Artbeschreibung: 30-100(-150) cm hoch, dichte Horste bildend. +Blaetter +2-4 mm +breit, +dunkelgruen +, flach, +oberseits mit scharf gekielten, sehr rauen Rippen +, dazwischen farbloses Gewebe (Durchlicht!). +Rand schneidend rau +. +Blatthaeutchen +6-8 mm +lang. + +Rispe +10-40 cm +lang, mit abstehenden, +/- geraden, rauen +Aesten + +. +Aehrchen +4-5 mm +lang, 2-3 +bluetig +, mit 2 +/- gleich langen, +haeutigen +Huellspelzen +. Deckspelzen +haeutig +, mit kurzer, die Spelze nicht +ueberragender +Granne. + + + + +Bluetezeit +: 6-8 + + +Standort und Verbreitung in der Schweiz: Feuchte +Boeden +, +Wegraender +, Ufer, +Waelder +/ kollin-alpin / CH + + + +Verbreitung global: Weltweit verbreitet + + + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +sehr feucht; Feuchtigkeit stark wechselnd (mehr als ++/- +2 Stufen) +Lichtzahl LhalbschattigSalzzeichen--
Reaktionszahl RxTemperaturzahl T +montan ( +Waelder +mit Buche, Weisstanne, in den Zentralalpen mit +Waldfoehre +) +
+Naehrstoffzahl +N + +maessig +naehrstoffarm +bis +maessig +naehrstoffreich + +Kontinentalitaetszahl +K + +subozeanisch bis subkontinental (mittlere Luftfeuchtigkeit, +maessige +Temperaturschwankungen und +maessig +tiefe Wintertemperaturen) +
+
+
+ + +Volksname Deutscher Name: +Rasen-Schmiele +, +Horstbildende Schmiele +Nom +francais +: +Canche cespiteuse +Nome italiano: +Migliarino maggiore + + +
+
\ No newline at end of file diff --git a/data/38/D0/7E/38D07E1FF0A5751E3096176EF96F55AC.xml b/data/38/D0/7E/38D07E1FF0A5751E3096176EF96F55AC.xml new file mode 100644 index 00000000000..016bff2db67 --- /dev/null +++ b/data/38/D0/7E/38D07E1FF0A5751E3096176EF96F55AC.xml @@ -0,0 +1,155 @@ + + + +One the genus Tocama Reitter (Coleoptera, Scarabaeidae, Melolonthinae), with descriptions of two new species from Indochina + + + +Author + +Li, Chun-Lin + + + +Author + +Wang, Chuan-Chan + + + +Author + +Keith, Denis + + + +Author + +Yang, Ping-Shih + +text + + +ZooKeys + + +2012 + +177 + + +37 +48 + + + + +http://dx.doi.org/10.3897/zookeys.177.2482 + +journal article +http://dx.doi.org/10.3897/zookeys.177.2482 +1313-2970-177-37 + + + + +Tocama laosensis Li & Keith +sp. n. +Figs 14610-12 + + + +Holotype + +male. LAOS: Lak 20, 22-26/VIII/1996, by local collector (deposited at Museum +fuer +Naturkunde der Humboldt Universitat (ZMHB), Berlin, Germany) + + + +Type locality. + +Southern Laos: Champasack province, Lak 20, +15°01'N +, +105°90'E +. + + + +Diagnosis. + +Tocama laosensis +is distinguished from other congeners by the following combination of characters: body medium sized, thin, pronotum flat when viewed laterally (Fig. 4); head, pronotum and scutellum blackish brown, elytra dull castaneous; surface of pronotum, scutellum and elytra covered with tiny brownish grey setae, setae on vertex about 4 times length of those on pronotum and elytra; basal margin of elytra between scutellum and humeral umbone broadly ridged (Fig. 6); apical ridge of pygidium impressed and becoming concave inwardly along plane of disc; mesometasternal process vestigial; metepimeron and sides of abdominal sternites 1-6 with maculation consisting of brownish white, scale-like setae; male genitalia as in Figures 10-12. + + + +Description. + +Males(Figs 1, 4): BL: 20.0 mm; BW: 12.0 mm; CL/BL=1.1; PgW/L= 1.32. Body thin, pronotum flat when viewed laterally (Fig. 4). Head, antennae, pronotum, scutellum and venter blackish brown; tarsomeres black; elytra dull castaneous; dorsal surface of body covered with minute, brownish grey setae. Head: Surface densely and coarsely punctate, each puncture with a seta, setae on clypeus thinner and shorter than those on vertex. Clypeus rectangular, bordered, with center apex emarginated; vertex slightly convex with setae about 4 times length of those on pronotum and elytra. Antennal club straight, subequal in length to basal segments. Labrum strongly bilobed at middle, symmetrical, each lobe rounded apically. Mentum with anterior margin moderately bilobed, surface sparsely setigerous, setae moderately long. Maxillary palpi short, apical palpomere about half length of antennomere 3. Pronotum: wider than long, widest at base, depressed when viewed laterally (Fig. 4); lateral margins well bordered, weakly developed anterior to scutellum; surface densely, evenly punctuate; punctures fine, each with a scale-like, tiny seta about 3 times length of diameter of puncture. Scutellum semicircular, surface with punctures and setae similar to those on pronotum. Elytron: Widest at middle; surface rugose with 4 weakly developed, punctate costae, costae 1-3 (starting from suture) complete, costa 4 vestigial; overall punctures and setae same as those on disc of pronotum; basal margin of elytra between scutellum and humeral umbone broadly ridged (Fig. 6). Propygidium: Surface densely punctate, punctures setigerous, setae similar to those on disc of pronotum with a row of more robust setae along apical margin. Pygidium: Lateral margins narrowly flattened. Surface densely punctuate; punctures setigerous, setae scale-like, longer and +more +robust than those on pronotum, sparsely intermixed with hair-like, long setae (about 3-12 times longer than scale-like setae); pygidial apex truncate and concave inwardly along plane of disc (see Fig. 8 for +Tocama procera +), apical margin weakly quadrate. Venter: Prosternal process feebly protruding, apex not reaching base of protrochanter. Mesometasternal process vestigial. Metepisternum densely covered with hair-like setae. Metepimeron and sides of abdominal sternites 1-6 with maculation of brownish white, scale-like setae. Middle of abdominal sternites 1-4 almost impunctate, sides densely punctuate; punctures setigerous, setae fine, scale-like, intermixed with hair-like setae that are 3-15 times longer. Legs: Protibia tridentate with basal tooth weakly developed. Pro- and mesofemora flattened, surface hairy; hind femora stout, broad, surface clothed with much shorter, robust setae than those of pro- and mesofemora. Mesotibia with 2 apical spurs equal in length. Metatibia with dorsal apical spur reaching to middle of metatarsomere 2; ventral apical spur of metatibia subequal in length to metatarsomere 1. Parameres: In lateral view (Figs 10, 12), base of parameres (BP) constricted, ventroapical swelling of right paramere (RPvs) weakly developed. Middle of lateral margin smooth when viewed dorsally (Fig. 11). + + + +Figures 1-3. Dorsal habitus of +Tocama +spp. 1 +Tocama laosensis +sp. n., holotype male 2 +Tocama procera +sp. n., holotype male 3 +Tocama procera +sp. n., paratype female. + + + + +Figures 4-5. Right lateral view of +Tocama +spp. 4 +Tocama laosensis +sp. n., holotype male 5 +Tocama procera +sp. n., holotype male. + + + + +Figures 6-7. Base of right elytron of +Tocama +spp. 6 +Tocama laosensis +7 +Tocama procera +. Prm, pronotum; Sc, scutellum; Elyt, elytron. + + + + +Figures 8-9. Right oblique view of pygidium of +Tocama procera +8 holotype male. 9 paratype female. + + +Female unknown. + + +Etymology. + +The species epithet is derived from the name of Laos, wherefrom it is described. This is the first +Tocama +species from this country and is probably endemic to it. + + + +Remarks. + +Tocama laosensis +is known from a single male specimen collected by a local collector, and it lacks further information. However, the type locality of the species is the southernmost distribution for the genus so far. + + + + \ No newline at end of file diff --git a/data/38/D0/BB/38D0BB4A0D839623818E1DBCEA1FD9AB.xml b/data/38/D0/BB/38D0BB4A0D839623818E1DBCEA1FD9AB.xml new file mode 100644 index 00000000000..72cfaa3fc1b --- /dev/null +++ b/data/38/D0/BB/38D0BB4A0D839623818E1DBCEA1FD9AB.xml @@ -0,0 +1,375 @@ + + + +Info Flora Schweiz - Asteraceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/asteraceae.html + +url + + + + + +Aster lanceolatus +Willd. + + + + + + +Lanzettblaettrige +Aster + + + + + +Art ISFS: 52100 Checklist: 1005680 +Asteraceae +Aster +Aster novi-belgii +aggr. +Aster lanceolatus Willd. + + + +Bestimmungsschluessel + + + +Zusammenfassung + + + + +Artbeschreibung + +(nach +Lauber & al. 2018 +) + +: +Aehnlich +wie + +A. novi-belgii + +, aber +Blaetter +mit abgerundetem Grund sitzend, seltener etwas umfassend, + +Huelle +nur +4-6 mm +lang + +, +aeussere +Huellblaetter +hoechstens +halb so lang wie die inneren, hell berandet. +Gruenes +Mittelfeld lanzettlich, bis zum Grund +allmaehich +verschmalert. Innere +Huellblaetter +allmaehlich +und lang zugespitzt (bei + +A. novi-belgii + +nach oben verbreitert und +ploetzlich +zugespitzt), + +Zungenblueten +weiss bis lila + +. + + + + +Bluetezeit + +(nach +Lauber & al. 2018 +) + +: 8-9 + + +Standort und Verbreitung in der Schweiz + +(nach +Lauber & al. 2018 +) + +: +Ufergebuesch +, +Auenwaelder +, +Schuttplaetze +, verwildert / kollin / + + + + +Verbreitung global + +(nach +Lauber & al. 2018 +) + +: Stammt aus Nordamerika + + + + +Oekologische +Zeigerwerte + +(nach +Landolt & al. 2010 +) + +3w + 44+34 + 2.g.2n=64 + + + + + +Oekologie + + +Lebensform Geophyt + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + + + + + +
KEINE ANGABE
+
+
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +maessig +feucht; Feuchtigkeit stark wechselnd (mehr als ++/- +2 Stufen) +Lichtzahl LhalbschattigSalzzeichen1
Reaktionszahl Rneutral bis basisch (pH 5.5-8.5)Temperaturzahl Twarm-kollin
+Naehrstoffzahl +N + +naehrstoffreich + +Kontinentalitaetszahl +K +subozeanisch (hohe Luftfeuchtigkeit, geringe Temperaturschwankungen, eher milde Winter)
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Aster lanceolatus +Willd. + + + + + + +Volksname Deutscher Name: + +Lanzettblaettrige +Aster Nom + +francais +: + +Aster +lanceole + +Nome italiano: +Astro lanceolato + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Aster lanceolatus Willd. + + +Checklist 2017 + +52100
= +Aster lanceolatus Willd. + + +Flora Helvetica 2018 + +2027
= +Aster lanceolatus Willd. + + +SISF/ISFS 2 + +52100
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Kommentare aus der +Checklist 2017 +Neuer Status: Das Taxon hatte im SISF-2 den Status +"I" +eines eingeschlossenen Namens und ist neu als +gueltiger +Name akzeptiert. Checklist + + + + +Status Indigenat +: Neophyt: nach der Entdeckung von Amerika in der Region aufgetreten (nach 1500) + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein +Art der "Liste der invasiven gebietsfremden Arten" + + +
+
\ No newline at end of file diff --git a/data/38/D1/3A/38D13A40CE1555FEBC036676554C5B7C.xml b/data/38/D1/3A/38D13A40CE1555FEBC036676554C5B7C.xml new file mode 100644 index 00000000000..8fff09af34f --- /dev/null +++ b/data/38/D1/3A/38D13A40CE1555FEBC036676554C5B7C.xml @@ -0,0 +1,75 @@ + + + +A checklist of vascular plants of the W National Park in Burkina Faso, including the adjacent hunting zones of Tapoa-Djerma and Kondio + + + +Author + +Nacoulma, Blandine M. I. +Universite Joseph Ki-Zerbo, Ouagadougou, Burkina Faso + + + +Author + +Schmidt, Marco +Senckenberg Biodiversity and Climate Research Centre, Frankfurt am Main, Germany & Palmengarten, Frankfurt am Main, Germany +https://orcid.org/0000-0001-6087-6117 +mschmidt@senckenberg.de + + + +Author + +Hahn, Karen +Goethe University, Frankfurt am Main, Germany + + + +Author + +Thiombiano, Adjima +Universite Joseph Ki-Zerbo, Ouagadougou, Burkina Faso + +text + + +Biodiversity Data Journal + + +2020 + +8 + + +54205 +54205 + + + + +http://dx.doi.org/10.3897/BDJ.8.e54205 + +journal article +http://dx.doi.org/10.3897/BDJ.8.e54205 +1314-2828-8-e54205 +AC04300B71A5532C90F2702393102067 + + + + +Crinum ornatum (Aiton) Herb. + + + +Distribution +Pluriregional African + + +Notes +Life Form: geophyte; Voucher: Nacoulma (APPG-69869) + + + \ No newline at end of file diff --git a/data/38/D2/A6/38D2A64F70A10B9CDE7F214339AFB2E3.xml b/data/38/D2/A6/38D2A64F70A10B9CDE7F214339AFB2E3.xml new file mode 100644 index 00000000000..77da9ffb9c5 --- /dev/null +++ b/data/38/D2/A6/38D2A64F70A10B9CDE7F214339AFB2E3.xml @@ -0,0 +1,42 @@ + + + +Species plantarum: exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas + + + +Author + +Linnaeus, Carolus + +text + +1753 +Laurentius Salvius + +Stockholm + + + +https://doi.org/10.5962/bhl.title.669 + +book +10.5281/zenodo.3931989 +3931989 + + + + +Alchemilla alpina var. hybrida +, +var. nov. + + + + +β. Alchemilla alpina pubescens minor. +Tournef. inst. 508. Pluk. phyt. 240. f.1. + + + + \ No newline at end of file diff --git a/data/38/D3/8A/38D38A2B57C95F2EA33C80851058793D.xml b/data/38/D3/8A/38D38A2B57C95F2EA33C80851058793D.xml new file mode 100644 index 00000000000..8e0ec123bd0 --- /dev/null +++ b/data/38/D3/8A/38D38A2B57C95F2EA33C80851058793D.xml @@ -0,0 +1,190 @@ + + + +A review of the genus Orthocentrus Gravenhorst (Hymenoptera, Ichneumonidae, Orthocentrinae) from South Korea + + + +Author + +Humala, Andrei E. +https://orcid.org/0000-0001-8741-254X +Forest Research Institute, Karelian Research Centre, Russian Academy of Sciences, 185910, Petrozavodsk, Russia + + + +Author + +Lee, Jong-Wook +https://orcid.org/0000-0002-8684-3935 +Department of Sciences, Yeungnam University, Gyeongsan, 38541, Korea + + + +Author + +Choi, Jin-Kyung +https://orcid.org/0000-0002-4059-0645 +Department of Science Education, Daegu National University of Education, Daegu, 42411, Korea +258aa@ynu.ac.kr + +text + + +Journal of Hymenoptera Research + + +2020 + +2020-02-27 + + +75 + + +15 +65 + + + + +http://dx.doi.org/10.3897/jhr.75.47006 + +journal article +http://dx.doi.org/10.3897/jhr.75.47006 +1314-2607-75-15 +69D2154C21AC463DA0B4A56ACAF37FE3 +FD279561ED4452F38110D24FF51D441D +3698453 + + + + +6. +Orthocentrus flavescens Humala & Lee +sp. nov. + + + + +Fig. 5 + + + +Description. + +Female. +Fore wing length 3.1 mm. + + +Face at level of antennal sockets 1.4 times as wide as high; face smooth, polished, sparsely punctate, eyes not setose, dorsal ridge of face in between antennal sockets with a median blunt low prominence; face profile straight except dorsally very slightly impressed, inner orbits slightly divergent ventrally; edge of clypeus straight, antennal sockets not on a distinct high shelf; subocular sulcus well developed, nearly straight; maxillary palp reaching beyond fore coxa. In dorsal view, head posteriorly slightly concave, temples very short, lateral ocellus separated from eye by a distance 1.4 times longer than its maximum diameter, POL 1.6 times as long as diameter of lateral ocellus; ocellar-ocular grooves present. Minimum distance between antennal sockets about 0.4 +x +diameter of socket; antenna with 20 flagellomeres elongate, first flagellomere about 3.0 times as long as wide and about 0.9 times as long as scape; scape slightly convex on inner surface, slightly concave on outer surface. + +Mesosoma smooth and polished; mesoscutum anteriorly with distinct notauli; in profile, scutellum particularly high, metapleuron slightly convex; propodeum with posterior transverse carina complete, strong and raised between lateral longitudinal carinae, lateromedian longitudinal carinae complete, lateral longitudinal carinae distinct, spiracle small. +Legs robust; coxae polished, femora with coriaceous microsculpture, tibiae and tarsi coriaceous-granulate; hind femur 2.9 times as long as high, hind tibia 3.5 times as long as apically wide; tibiae with spine-like setae. +Wings not particularly narrow; fore wing without areolet; vein Rs nearly straight, fore wing with vein Rs+2r meeting middle of pterostigma; vein cu-a nearly interstitial (opposite Rs&M); nervellus straight, intercepted below. +First tergite stout, widening posteriorly, 1.2 times as long as posteriorly wide; coriaceous, with two lateromedian longitudinal carinae and longitudinal striae, with transverse impressions originating at about middle of tergite, sloping posteriorly, meeting centrally. +Second tergite 0.8 times as long as posteriorly wide; coriaceous and longitudinally striate, with developed lateromedian longitudinal carinae, anterior corners impressed and transverse groove near posterior margin bending anteriorly near lateral margins, forming a somewhat uplifted striated area medially; small thyridia contrastingly coloured. Third tergite longitudinally striate with transverse impressions originating at about middle of tergite, sloping posteriorly, not meeting centrally. Remainder of metasoma unsculptured, polished. Ovipositor thin, comparatively short, weakly upcurved, without subapical dorsal notch; ovipositor sheath narrow, with sparse setae. +Body setose except eyes, pronotum, mesopleuron and metapleuron, setae scattered on metasoma and posterior sides of coxae. +Yellowish brown; face dusky orange, inner orbits broadly yellow up to occiput; antenna yellowish-brown; malar area yellow posterior to subocular sulcus and up to level of eye middle; mouthparts, legs yellow; propleuron, pronotum, mesopleuron in lower 2/3, mesoscutum anteriorly and longitudinal bars along notauli, scutellum, central part of metapleuron, reddish brown; posterior margins of tergites 1-3 and tergite 4 light-brown. + +Male. +flagellum with 21 flagellomeres; basic coloration - yellow, frons reddish-yellow. Otherwise as in female. + + + +Biology. +Hosts unknown. + + +Etymology. + +Named from the Latin +flavesco +(turn yellow) after the yellowish general body colouration. + + + +Comparison. + +This is a distinctive species on account of the metasomal tergites 2-3 with strong transverse-diagonal furrows separating contrastingly coloured creamy latero-posterior corners. From the closely allied + +O. castellanus + +it differs in the absence of the fore wing areolet and fewer antennal flagellomeres. + + + +Material examined. + + + +Holotype + +: female; +South Korea +, +GW +: +Chuncheon-si +, +Sanong-dong +, +Gwangwon Provincial Arboretum +, +1-14.VIII.2013 +, +I.G. Kim +leg. (DNUE). + + + + + +Paratype + +: +South Korea +, +GB +: +1 ♂ +, Bongjeongsa +10-11.VII.1998 +, +J.W. Lee +leg. (DNUE-0135) + +. + + + +Distribution. +South Korea (GB, GW). + + +Figure 5. + +Orthocentrus flavescens + +sp. nov. Holotype. +A +Habitus in lateral view +B +head in frontal view +C +head in dorsal view +D +head and mesosoma in lateral view +E +mesosoma in dorsal view +F +areolet +G +first to third tergites in dorsal view. + + + + + \ No newline at end of file diff --git a/data/38/D3/C5/38D3C55856D018E295E9E0473237A6D1.xml b/data/38/D3/C5/38D3C55856D018E295E9E0473237A6D1.xml new file mode 100644 index 00000000000..f4c18742a3c --- /dev/null +++ b/data/38/D3/C5/38D3C55856D018E295E9E0473237A6D1.xml @@ -0,0 +1,93 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part A) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +252 +342 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Antirrhinum viscosum +Linnaeus + +, + +Centuria II Plantarum + +: 21. 1756 + + +. + + + +"Habitat in Hispania." RCN: 4445. + + + + +Lectotype +(designated here by Sutton): Herb. Linn. No. 767.24 ( +LINN +) + +. + + + + +Current name: + + +Linaria viscosa + +(L.) Chaz. + +( +Scrophulariaceae +). + + + + +Note: +Viano (in +Candollea +33: 57. 1978) wrongly indicated both 767.24 and 767.25 (LINN) as syntypes. + + + + \ No newline at end of file diff --git a/data/38/D4/63/38D4639FAC5F0420694C6720BC05A6D1.xml b/data/38/D4/63/38D4639FAC5F0420694C6720BC05A6D1.xml new file mode 100644 index 00000000000..1dd934db5cf --- /dev/null +++ b/data/38/D4/63/38D4639FAC5F0420694C6720BC05A6D1.xml @@ -0,0 +1,652 @@ + + + +Antispila oinophylla new species (Lepidoptera, Heliozelidae), a new North American grapevine leafminer invading Italian vineyards: taxonomy, DNA barcodes and life cycle + + + +Author + +Nieukerken, Erik J. van + + + +Author + +Wagner, David L. + + + +Author + +Baldessari, Mario + + + +Author + +Mazzon, Luca + + + +Author + +Angeli, Gino + + + +Author + +Girolami, Vicenzo + + + +Author + +Duso, Carlo + + + +Author + +Doorenweerd, Camiel + +text + + +ZooKeys + + +2012 + +170 + + +29 +77 + + + + +http://dx.doi.org/10.3897/zookeys.170.2617 + +journal article +http://dx.doi.org/10.3897/zookeys.170.2617 +1313-2970-170-29 + + + + +Antispila oinophylla Van Nieukerken & Wagner +sp. n. +Figs 1 +-69- +296263 + + + + +Antispila +sp.; +Baldessari et al. 2009 +: 68 [first record for Italy]; +Duso et al. in press +[pest status]. + + +Antispila ampelopsifoliella +; +Needham et al. 1928 +: 289 [partim]; +Davis 1983 +: 4 [partim]; +van Nieukerken 2011 +: Fauna Europaea database; + +Lastuvka +2009 + +: S57; +van Nieukerken et al. 2011a +: 51. Misidentifications. + + +Antispila ampelopsiella +; +Dyar et al. 1903 +: 539 [partim]; +Barnes and McDunnough 1917 +: 181 [partim]; +Forbes 1923 +: 226 [partim]; +McDunnough 1939 +: 91 [partim]; +Brower 1984 +: 29 [partim]. Misidentifications. + + + +Type material. + +Holotype ♂, USA: Georgia, Murray Co., Chattahoochee Nat. Forest, E of Chatsworth, GA rd 52, 523 m, +34.74066N +, +84.71852W +, hardwood forest along highway, leafmines on +Vitis aestivalis +var. aestivalis, 14.x.2010, EvN2010266, emerged 14. +iv- +4.v.2011, E.J. van Nieukerken & C. Doorenweerd, Genitalia slide EJvN 4204, RMNH.INS.24204 (RMNH). + + + +Paratypes. + +32♂, 31♀. Italy: 1♂, 3♀ (all dissected), Trento, Borgo Valsusana, leafmines 2007, on +Vitis vinifera +, emerged 1. +iii- +26.iv.2008, M. Baldessari; 3♀, same locality, 13.viii.2008; 10♂, 1♀ (1♂ RMNH.INS.23920 dissected & DNA barcode), same locality, 18.viii.2008; 17♂, 18♀ (1♂ RMNH.INS.24038, 1♀ RMNH.INS.24039 dissected & DNA barcode), same locality, 29.vi.2009, leafmines on +Vitis vinifera +, EvN no 2009903, emerged in Leiden, 14. +vii- +6.viii.2009, M. Baldessari (all RMNH). Canada: 1♂, Ontario, Ottawa, mines on +Vitis +, rearing 57-112, emerged 31.iii.1958, Freeman & Lewis (CNC); 1♀, Quebec, Hull, mines on +Vitis +, rearing 55-228, emerged 26.vi.1956, T.N. Freeman (CNC). USA: 1♂, Connecticut +, +Tolland Co., Mansfield, 22.viii.1989, leafmines on Vitis, DLW89H37 breeding, emerged 4.v.1990, D.L. Wagner (DLW); 1♀ (dissected), Connecticut, Windham Co., Hampton, 916 Pudding Hill Rd., leafmines on +Vitis +1-5.ix.1988, DLW 88J7, emerged 20.vii.1989, D.L. Wagner (DLW); 1♂ 1 ♀, Georgia, same data as holotype; 1♀, Georgia, Murray Co., Chattahoochee Nat. Forest, Cohutta Overlook, 730 m, +34.785356N +, +84.627323W +, shrub in forest clearing, leafmines on +Vitis aestivalis +var. bicolor, 14.x.2010, EvN2010270, emerged 19.iv.2011, E.J. van Nieukerken & C. Doorenweerd (RMNH); 1♀ (dissected, EvN 4211), Kentucky, [Covington], bred, [19th century], Chambers, +"pseudotype," +MCZ Type 1367 (MCZ); 1♂, 1♀ (♂ dissected), Vermont, Chittenden Co., South Burlington, leafmines on +Vitis +11.viii.1988, DLW 88H23, emerged 30. +iii- +15.v.1989, D.L. Wagner (DLW). + + + +Non-type material + +(all in RMNH).Italy: leafmines & larvae, Borgo Valsusana, 29.vi.2009, on +Vitis vinifera +, EvN no 2009903, M. Baldessari. USA: 1 larva, Connecticut, Tolland Co., Storrs campus, on +Vitis labrusca +, 185 m, 8.ix.2011, EvN2011168, B. Gagliardi; leafmines and larvae (being reared), Connecticut, New London Co., Connecticut College Arboretum, 34 m, +41.37929N +, +72.11121W +, on +Vitis labrusca +, 10.ix.2011, EvN2011193, E.J. van Nieukerken; leafmines and larvae (being reared), Connecticut, New Haven Co., West Rock Ridge SP, 125 m, +41.33353N +, +72.96423W +, on +Vitis aestivalis +var aestivalis, 10.ix.2011, EvN2011198, E.J. van Nieukerken; leafmines & larvae (DNA barcode RMNH.INS.18394), Georgia, same data as holotype; leafmines & larvae (DNA barcode RMNH.INS.18392), Georgia, Murray Co., Chattahoochee Nat. Forest, Cohutta Overlook, 730 m, +34.78535N +, +84.62732W +, shrub in forest clearing, leafmines on +Vitis aestivalis +var. bicolor, 14.x.2010, EvN2010270, E.J. van Nieukerken & C. Doorenweerd (RMNH); leafmines & 2 larvae (DNA barcode RMNH.INS.18533), Massachusetts, Berkshire Co., Beartown State forest, SW margin, 480 m, +42.19814N +, +73.28928W +, on +Vitis riparia +, 12.ix.2011, EvN2011208, E.J. van Nieukerken; leafmines & larvae (DNA barcode RMNH.INS.18558), New York, Essex Co., Hwy 9N, 3.5 km WSW Keeseville, 142 m, +44.49233N +, +73.52042W +, on +Vitis riparia +, 14.ix.2011, EvN2011237, E.J. van Nieukerken; leafmines & larvae (DNA barcode RMNH.INS.18555), New York, Essex Co., Wilsboro, Noblewood Park, 62 m, +44.35216N +, +73.36435W +, on +Vitis riparia +, 14.ix.2011, EvN2011244, E.J. van Nieukerken; leafmines & larvae (DNA barcodes RMNH.INS.18298, 18300), Tennessee, Blount Co., NP Great Smoky Mts, Rich Mountain Gap, 619 m, +35.64557N +, +83.80537W +, rich forest on limestone ridge, leafmines on +Vitis vulpina +, 2.x.2010, EvN2010119, E.J. van Nieukerken & C. Doorenweerd (RMNH); mine and larva, (DNA barcode LGSME035-06), Tennessee, Cocke Co., Cosby, ATBI house, +35.77771N +, +83.21359W +, on +Vitis +sp. 12.viii.2006, DLW 2006H55, D.L. Wagner (DLW); leafmines & larvae (being reared and DNA barcode RMNH.INS.18669), Vermont +, +Addison Co., Button Bay SP, Lake Champlain borders, 44 m, +44.18154N +, +73.36892W +, on +Vitis riparia +, 16.ix.2011, EvN2011253, E.J. van Nieukerken. + + + +Differential diagnosis. + +In North America, at least four other species have an apical silver spot (together forming the ampelopsifoliella group): +Antispila ampelopsifoliella +, +Antispila voraginella +, which has a darker head, an unnamed species from +Vitis +(here +Antispila +"vitis2" +) and +Antispila hydrangaeella +Chambers, 1874. The latter, which is closely similar in appearance, can be separated by the greater number of white flagellomeres at the antennal tip (six segments) and feeds on +Hydrangea arborescens +L. ( +Hydrangeaceae +). Dissection of genitalia is needed to distinguish +Antispila oinophylla +from other members of the ampelopsifoliella group. Male genitalia are characterised by the long carinal spine at the phallotrema and several other details; female genitalia differ by the number of cusps on the ovipositor from at least +Antispila ampelopsifoliella +. + + +In Europe, +Antispila oinophylla +differs from all other +Heliozelidae +with a similar forewing colour pattern (species of +Antispila +, +Antispilina +and +Holocacista +) by the presence of a small silvery spot in the apical part of forewing and the distinctly white head. Some +Elachistidae +are superficially similar, but differ in long-pointed and upcurved palpi, longer antennae and more elongate habitus. + + +The leafmine of +Antispila oinophylla +differs from that of +Holocacista rivillei +by its short initial gallery, which is later usually completely incorporated into the blotch, whereas the initial gallery of +Holocacista rivillei +mines is usually as long as or longer than the blotch, and remains intact. In Eastern North America other +Vitis +-feeding +Antispila +do not show the concentric arrangement of frass that is typical for +Antispila oinophylla +- particularly in thinner leaves -and the mines are often larger. Mines of +Antispila +cf isabella and related species are much larger, and also have much larger cut-outs, 5 mm or longer. Since not all +Vitis +miners have been comprehensively studied, mine identification cannot yet be relied on. + + + +Description. +Adult (Figs 1-5). Head face and vertex covered with appressed, strongly metallic, silvery-white scales, more prominently raised in male. Palpi porrect, white; base of proboscis covered with white scales. Antenna fuscous, apical 1 or 2 flagellomeres white. Labial palp silvery white, slightly upturned. Thorax lead-coloured, shiny, contrasting with forewings. Legs grey, tarsi mostly yellowish white, especially on undersides. Forewing dark fuscous with silver-golden patterning; an outwardly oblique fascia from 1/8 of posterior margin to 1/4 of costa, narrowing towards costa; triangular (dorsal) spot at middle of posterior margin, reaching to middle of wing, smaller triangular costal spot just beyond middle, sometimes touching dorsal spot; small, silvery subapical spot in middle of wing at 3/4; fringe line distinct. Terminal fringe paler. Hindwing pale grey. Abdomen lead-coloured, including vestiture on external genitalia. + + +Figures 1-5. +Antispila oinophylla +, adult habitus. 1 Male holotype, RMNH.INS.24204 2 Female paratype, RMNH.INS.24039, Italy, Borgo Valsusana. 3-5 Alive male,Georgia, paratype, emerged 29.iv.2011. + + + +Measurements: male: forewing length 2.5-2.8 mm (2.6 ++/- +0.10, n=11), wingspan 5.5-6.2 mm, 25-31 antennal segments (29.1 ++/- +1.9, n=11); female: forewing length 2.3-2.8 mm (2.5 ++/- +0.16, n=10), wingspan 4.8-5.6 mm, 25-29 antennal segments (27.2 ++/- +1.4, n=8). + + +Venation (Fig. 6). Forewing with Sc barely visible. R1 a separate vein, connected by persistent trachea to Rs+M stem. Rs+M terminating in five branches, interpreted +as +Rs2 (possibly with 1) to costa, Rs3+4 to costa just before apex, M1 to dorsum just beyond apex, M2+3 to dorsum and a weakly developed CuA. A1+2 a strong separate vein. Hindwing with Sc barely or not visible, Rs+M a strong vein, bifurcate from ca. 1/4th, upper vein ending in two branches: Rs and M1, lower vein single (M3); Cu and A1+2 separate veins. + + +Compared to the complicate venation of many other +Antispila +species, including the type species +Antispila metalella +, (example in Fig. 7, +Antispila treitschkiella +) venation reduced with loss of forewing cell, separate M stem and connection between R1 and Rs, loss of Rs1 and in hindwing loss of M2. The venation more closely resembles that of +Holocacista rivillei +(Fig. 8), which is even more reduced and also lacks Cu in the forewing. + + + +Figures 6-7. +Antispila +, venation. 6 +Antispila oinophylla +, male, Italy, RMNH.INS.24257 7 +Antispila treitschkiella +, male, Netherlands, Leiden, RMNH.INS.24258. + + + + +Figure 8. +Holocacista rivillei +, venation.Female, Italy, RMNH.INS.24259. + + +Male genitalia (Figs 9-16). Uncus bar-shaped, with two large setae dorsally. Vinculum very long, anteriorly rounded, posteriorly shallowly bilobed. Valva more or less triangular, pecten on pedicel, with 10-13 comb teeth (Fig. 15); inner margin of valva with setose lobe anterior to pecten pedicel; basally with a triangular protuberance, almost touching that of other valva; transtilla with trapezoid medial plate, sublateral processes relatively short. Juxta anteriorly spade-shaped, about half as long as phallus. Phallus long, anteriorly much widened, at phallotrema with a comb of about 10-12 strong teeth and at left side a very long curved process (Figs 10-12, 16). + + +Figures 9-16. +Antispila oinophylla +, male genitalia.Paratype, Italy,RMNH.INS.23920 (9, 15, 16), Paratype, Italy, RMNH.INS.15247 (12),Holotype, RMNH.INS.24204 (10, 11, 13-14). 9 Complete genitalia with separate phallus in ventral view 10-12 Phallus and juxta in ventro-lateral view 15-16 Complex of tegumen, uncus, valvae and transtilla 15 Detail of valval tips and pectinifers 16 Detail of spines near phallotrema. + + +Female genitalia (Figs 17-20). Ovipositor with 4-5 cusps at either side (Fig. 19). S8 medially indented, with many papillate setal sockets. Vestibulum with broad, indistinct sclerotization and no spines (Fig. 18). + + +Figures 17-20. +Antispila oinophylla +, female genitalia. 17 Terminal segmentsandapophyses, ventral view, paratype, EJvN4211,USA, Kentucky (pseudotype ampelopsifoliella) 18 Internal genitalia, lateral view, showing sclerotisation in vestibulum,paratype, EJvN4206,USA, Connecticut 19 Ovipositor tip, dorsal view, EJvN4206 20 Detail of S8, ventral view,paratype, Italy,RMNH.INS.15244. + + + + +Biology. + +Host plants.In North America reared from or found as larva on summer grape +Vitis aestivalis +Michx., both var. aestivalis and var. bicolor Deam, fox grape +Vitis labrusca +L., riverbank grape +Vitis riparia +Michx. and frost grape +Vitis vulpina +L. Literature +records +of +Antispila +"ampelopsifoliella" +from +Vitis +or grape likely refer to this species ( +Chambers 1874a +, b +; +Forbes 1923 +; +Needham et al. 1928 +). We did not find any reports of this species occurring in vineyards in North America. In Italy mines produced by +Antispila oinophylla +were detected on various +Vitis vinifera +cultivars, hybrids (e.g. +Vitis riparia +x rupestris) and French-American grapes (e.g. Clinton). Infestation levels on the latter were comparable with those observed on commercial vineyards. A preference for some grape cultivars (e.g. Cabernet Sauvignon, Chardonnay, Muscat) is suggested from observations carried out in mixed cultivar vineyards. It is interesting that we also found active mines on Virginia creeper +Parthenocissus quinquefolia +in Italy (Levico and Caldonazzo, Trento province) (identification of larvae confirmed by DNA barcodes, no rearing attempted), whereas we have as yet no records of +Antispila oinophylla +from this host in North America. + + +Leafmines (Figs 21-28). The egg is inserted on the underside of a leaf, usually within 1-2 mm from a vein. The mine starts as a rather straight or slightly contorted gallery towards the vein, usually forms a right angle and often follows the vein for a short distance, then again turns away from the vein where it expands into a blotch. The gallery portion, of variable length, is usually later incorporated into the blotch mine. The frass is linear, usually occupies the complete mine width, but occasionally is deposited in a thin line (Fig. 27). In the blotch much of the blackish-brown frass is deposited close to the origin in semicircular concentric frass lines. This characteristic pattern is best seen in thin shade leaves (e.g., Figs 25, 26); in sun-exposed leaves the frass pattern is often obscured. The whole mine occupies as a rule an area of less than 10 +x +10 mm; only in thin leaves are mines appreciably larger. The larva cuts out an elliptic case of about 3.2-4.0 mm long. + + + +Figures 21-28. +Antispila oinophylla +, life history: leafmines on several species of +Vitis +and different localities. 21, 23, 24 Italy, Borgo Valsusana, +Vitis vinifera +, 25.vi.2009 22 USA: Vermont, Button Bay SP, +Vitis riparia +16.ix.2011 25 USA:Tennessee, NP Great Smoky Mts, +Vitis vulpina +, 2.x.2010, mine in shade leaf 26, 28 USA: Georgia, type locality, +Vitis aestivalis +var. aestivalis, 14.x.2010 27 USA: Vermont, Button Bay SP, +Vitis riparia +, 16.ix.2011, DNA barcode,RMNH.INS.18589. + + + + +Distribution + +(Fig. 29, 62). In North America, +Antispila oinophylla +is known with certainty (material cited) from Canada: Ontario, Quebec; USA: Connecticut, Georgia, Kentucky, New York, Tennessee, and Vermont. Records under +Antispila ampelopsifoliella +from Maine, Missouri, and Ohio ( +Brower 1984 +, +Forbes 1923 +) may partly refer to this species. In Europe introduced into northern Italy, see below. In our experience in the southern Appalachians and New England, at least in the fall, +Antispila oinophylla +is often the most abundant +Antispila +species occurring on +Vitis +. + + + +Figure 29. +Antispila oinophylla +, distribution in North America. + + + + +Etymology. + +The epithet oinophylla, a noun in apposition, is from the Greek +οινος +(oinos = wine) and +φυλλον +, plural +φυλλα +(phyllon, phylla = leaf), "wine leaves," because the larva lives in the leaves of the grapevine from which wine is made. + + + +Justification for status as new species. + +Four species feeding on +Vitaceae +have been named previously from North America. No name-bearing types are available for three species, only for +Antispila voraginella +is a holotype extant. The latter is clearly different from +Antispila oinophylla +, and restricted to western North America. For the eastern species +Antispila isabella +, +Antispila viticordifoliella +and +Antispila ampelopsifoliella +, we have only the original descriptions and subsequent interpretations to establish identities. The fact that our preliminary sampling of DNA barcodes for grape-feeding +Antispila +show great diversity, complicates matters further. Below, we will discuss these three species in the chronological order of their descriptions. + + + +Antispila +isabella + +was described from mines on "Isabella grape" (a cultivar of +Vitis labrusca +) and adults ( +Clemens 1860 +). The description unequivocally describes a relatively large species without a silvery apical spot. Clemens characterizes the case (shield) as large and almost roundish - both features exclude our species. We have tentatively named one larger barcode cluster as +Antispila +cf. isabella, because mines and adults conform to this description. + + +Antispila viticordifoliella +was also described by Clemens in 1860, from mines on "wild grapes" only, differing by a smaller case (shield) and a larva "without dots." Although the foodplant was not explicitly mentioned by Clemens, from the species name it is evident that the host must have been +Vitis cordifolia +Michx. (a synonym of +Vitis vulpina +). In fact his very brief description could fit the mines of +Antispila oinophylla +, but subsequently the name has always (e.g. +Forbes 1923 +) been used in the sense of +Chambers (1874a) +, who first described the moth (as "viticordifoliella N. sp.?"), without an apical spot and with several, white, distal flagellomeres. He reared that moth from the same hostplant ( +Vitis cordifolia +)as Clemens did, and was not able to find the mine on any other +Vitis +( +Chambers 1874a +: 169). One of the species that we studied from +Parthenocissus +has similar externals, and is named here +Antispila +cf viticordifoliella (Fig. 37). Because we +haven't +been able to find or rear any similar adults from +Vitis +we are at the moment unable to establish if the +Parthenocissus +miner is indeed the same as +Antispila viticordifoliella +, but clearly it is not our species (because it lacks an apical spot). In a future revision a neotype will need to be selected to firmly anchor the identity of this species, material from the +Chambers' +collection (two extant +"syntypes" +, see +Miller and Hodges 1990 +) probably is most suitable for that goal. In collections and websites (e.g., http://mothphotographersgroup.msstate.edu/) the name +Antispila viticordifoliella +is often misinterpreted as the species that we call +Antispila +cf isabella or a closely related one. + + +Antispila ampelopsifoliella +:Chambers(1874a: 168) only briefly described the mine and larva from " +Ampelopsis quinquefolia +" [= +Parthenocissus quinquefolia +] (and stated that he "never succeeded in breeding it."). Only a month later he described the moth under the name " +Antispila ampelopsisella +" [sic, considered as a subsequent incorrect spelling], writing: "Since that paper was placed in the hands of the Editor, many months ago, I have succeeded in rearing it from the mine [from +Parthenocissus +]" ( +Chambers 1874b +). Theconfusionof the new specieswith +Antispila ampelopsifoliella +dates from +Chambers' +original description, because he also described a moth that he reared from +Vitis +and shows the external characters of both species: + + +"Last summer I found its leaves [referring to a +Vitis +species] mined by a larva closely resembling that of +Antispila ampelopsifoliella +, supra, and which I suspect to be the same. +..... +From it I bred the species described below, which I do not now name, as it may prove to be identical with +Antispila ampelopsifoliella +." ( +Chambers 1874a +). One month later he wrote: "but I believe it to be the same" ( +Chambers 1874b +). Ever since these two publications, the species has been considered to feed both on +Parthenocissus +and +Vitis +(e.g., +Forbes 1923 +; +Brower 1984 +). However, our rearing and barcode data show that two or three species of +Antispila +are feeding on +Parthenocissus +, which show large barcode distances to +Antispila oinophylla +or other +Vitis +miners (Fig. 30), and thus are not identical. + + + +Figure 30. Neighbor-joining tree for heliozelid COI barcodes, based on uncorrected pairwise distances. Numbers on branches are bootstrap values, 10,000 replicates. +Vitaceae +-feeding clusters are coloured differently, others in black. Labels include species name or informal name, codes for country and state (in North America) and sample numbers (Genbank numbers for sequences taken from Genbank). + + + +In +Chambers' +collection at MCZ there are three specimens under the name +Antispila ampelopsifoliella +that probably served as the basis for the adult description. These specimens were termed pseudotypes ( +Miller and Hodges 1990 +), since they were not available at the time of the original description, because then Chambers only had mines and larvae available. Of the three specimens, one is completely missing from the pin. The one labelled as from +Parthenocissus +unfortunately is heavily damaged, only a forewing and hindwing being present. A third specimen, a female, is complete and was dissected (Fig. 17). This specimen, however, appears to be +Antispila oinophylla +. This is no surprise, since +Chambers (1874a +, +1874b +) considered the +Vitis +miner to be the same as the +Parthenocissus +miner, and thus he would have placed specimens reared from both hosts under the same name. There is no indication of the hostplant or the collecting year on this particular specimen, so it is useless for confirmation of the identity of +Antispila ampelopsifoliella +. + + +We restrict here the usage of the name +Antispila ampelopsifoliella +to the species feeding on +Parthenocissus +, with an apical spot (The generic name for +Parthenocissus quinquefolia +was +Ampelopsis +at the time Chambers described the species.) Although we have not obtained a DNA barcode form such an adult, the fact that an adult from the other cluster on this host (see below) does not have such a spot and is tentatively identified as +Antispila +cf viticordifoliella, we can associate +Antispila ampelopsifoliella +adults with one of the larval types. +When +adults are available for all barcode clusters, we suggest that a neotype be selected from material reared from +Parthenocissus +from the vicinity of Covington, Kentucky, to fix the identity of +Chambers' +name. + + + + \ No newline at end of file diff --git a/data/38/D4/9F/38D49FE8D1995D32A78B97CC0F7989C7.xml b/data/38/D4/9F/38D49FE8D1995D32A78B97CC0F7989C7.xml new file mode 100644 index 00000000000..3020128757a --- /dev/null +++ b/data/38/D4/9F/38D49FE8D1995D32A78B97CC0F7989C7.xml @@ -0,0 +1,81 @@ + + + +A contribution towards checklist of fungus gnats (Diptera, Diadocidiidae, Ditomyiidae, Bolitophilidae, Keroplatidae, Mycetophilidae) in Georgia, Transcaucasia + + + +Author + +Kurina, Olavi +https://orcid.org/0000-0002-4858-4629 +Institute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi st 5 D, 51006 Tartu, Estonia +olavi.kurina@emu.ee + +text + + +ZooKeys + + +2021 + +2021-03-26 + + +1026 + + +69 +142 + + + + +http://dx.doi.org/10.3897/zookeys.1026.63749 + +journal article +http://dx.doi.org/10.3897/zookeys.1026.63749 +1313-2970-1026-69 +05EFF10E62144368BE471AA57A2C38D7 +762AC1314DE05514BFD79A8DC8F34E2F + + + + +213. +Phronia humeralis Winnertz, 1863 + + + +Material. + +1♂ +, A-7; +1♂ +, SJ-4; +2♂♂ +, SJ-8; +2♂♂ +, SJ-9. Total: +6♂♂ +. + + + + +Distribution in +Georgia +. + + +Adjara, Samtskhe-Javakheti +. + + + +General distribution. +Palaearctic. + + + \ No newline at end of file diff --git a/data/38/D4/D9/38D4D98FE2B2BD2C080633900A4B435B.xml b/data/38/D4/D9/38D4D98FE2B2BD2C080633900A4B435B.xml new file mode 100644 index 00000000000..5ac9bc785c2 --- /dev/null +++ b/data/38/D4/D9/38D4D98FE2B2BD2C080633900A4B435B.xml @@ -0,0 +1,392 @@ + + + +Vatica najibiana (Dipterocarpaceae), a new species from limestone in Peninsular Malaysia + + + +Author + +Ummul-Nazrah, Abdul Rahman +Forest Research Institute Malaysia, 52109 Kepong, Selangor, Malaysia +ummul@frim.gov.my + + + +Author + +Mohd Hairul, Mohd Amin +Forest Research Institute Malaysia, 52109 Kepong, Selangor, Malaysia + + + +Author + +Kamin, Imin +Forest Research Institute Malaysia, 52109 Kepong, Selangor, Malaysia + + + +Author + +Kiew, Ruth +Forest Research Institute Malaysia, 52109 Kepong, Selangor, Malaysia + + + +Author + +Ong, Poh Teck +Forest Research Institute Malaysia, 52109 Kepong, Selangor, Malaysia + +text + + +PhytoKeys + + +2018 + +2018-05-10 + + +98 + + +99 +106 + + + + +http://dx.doi.org/10.3897/phytokeys.98.23903 + +journal article +http://dx.doi.org/10.3897/phytokeys.98.23903 +1314-2003-98-99 +FF968C752E7D003BFFECF22BAF53FFF7 +1249084 + + + + +Vatica najibiana Ummul-Nazrah +sp. nov. +Figures 1 +, 2 + + + +Diagnosis. + +Amongst the Vaticas with a half inferior ovary, it groups with + +Vatica harmandiana + +and +V. odorata (Griff.) Symington subsp. odorata +. + +Vatica harmandiana + +occurs on limestone hills and rocks but is different in having leaves that are elliptic-lanceolate, leaf base cuneate and nut diameter 7-10 mm as oppose to the obovate-elliptic leaf, leaf base cordate-subcordate and nut diameter of 5-6 mm in + +V. najibiana + +. +Vatica odorata subsp. odorata +is closely similar to the new species but can be separated by its elliptic-oblong leaf, leaf base obtuse, leaf apex acuminate, nut diameter 8-9 mm and occurrence in lowland and hill forest (Table +1 +). + + + +Table 1. +Differences between + +Vatica najibiana + +, +V. odorata subsp. odorata +and + +V. harmandiana + +. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Character + +V. najibiana + + +V. odorata subsp. odorata + + +V. harmandiana + +
HabitSmall tree to 5-7 mTall tree to 24 mTree, 15-24 m
Leaves
Petiole indumentumDark brownMid brown (reddish-brown)Pale brown
Lamina shapeObovate to ellipticElliptic to oblongElliptic to lanceolate
Lamina size (cm) +(3-)5-10.2 +x +1.5-5 + +8-16 +x +2.7-6 + +5.2-12 +x +(1.8-)2-5 +
Lamina baseCordate to subcordateObtuseCuneate
Lamina marginRecurvedNot recurvedNot recurved
Lamina apexAcuteAcuminateBlunt to acute
No. of lateral veins (pairs)(6-)7-109-157-8
Fruits
Calyx lobes length (cm) +2.3-3.3 +x +0.5-0.8 + +4-5.5 +x +1-1.5 + +2.6-7 +x +1-1.8 +
Nut Diameter (mm)5-68-97-10
HabitatLimestone onlyLowland and hill forestLimestone only
+
+
+ + +Type +. + + + +Peninsular +Malaysia +. +Kelantan +, +Gua Musang District +, +Relai Forest Reserve +(Ktn 50), +05°02'47.8"N +, +102°11'43.6"E +, +19 October 2016 +, Ummul-Nazrah et al. +FRI 86369 +( +holotype +KEP!; isotypes K!, SAN!, SING!) + +. + + + +Figure 1. + +Vatica najibiana + +. +A +Plant in its natural habitat +B +Bole +C +Inner bark +D-E +Leafy shoots with infructescences +F +Fruit. (Photographs by K. Imin & A.R. Ummul-Nazrah). + + + + +Figure 2. + +Vatica najibiana + +. +A +Leafy shoot with fruits +B +Calyx +C +Petal +D-E +Fruit +F +Long & short calyx lobes of fruit +G +Stellate hair +H +Fruit nut. (Drawn by N. Mohamad-Aidil from Ummul-Nazrah et al. +FRI 86369 +). + + + + +Description. + +Small tree, 5-7 m tall; bole to 15-17 cm diameter, without buttresses. +Bark +smooth with faint horizontal rings, dark brown with white lichen patches; inner bark pale yellow, exuding clear sap when cut. +Twigs +robust, 3-5 mm diameter, covered with 6-15-armed stellate hairs, 94-169 +µm +diameter, glabrous when mature, older twigs terete. +Leaves +when young brown rusty beneath, glabrous when mature; petioles 0.8-1.5 cm long, 0.1-0.2 cm wide, densely covered with stellate hairs, caducous when mature, drying dark brown; lamina obovate to elliptic, (3-)5-10.2 +x +1.5-5 cm, thickly chartaceous, bullate, green on both surfaces when fresh, base cordate to subcordate, margin entire and recurved, apex acute; midrib prominent on both surfaces; lateral veins (6-)7-10 pairs, prominent below, slightly raised and visible above, ascending to margin; intercostal veins reticulate-scalariform and slightly conspicuous on both surfaces. +Flowers +: (dry) pedicels with velvety brown stellate hairs; calyx 5-lobed, elliptic, 4-7 +x +ca. 1 mm, densely covered with stellate hairs on both surfaces, apex acute; petals narrowly elliptic, ca. 6 +x +2 mm, glabrous outside, inside from base to tip completely covered with 6-10-armed stellate hairs, 77-120 +µm +diameter. +Infructescence +axillary, near apex of leafy shoot, ca. 4 cm long, densely covered with rusty stellate hairs, branching once or twice, densely covered with stellate hairs; first branches with 1-7 fruits along axis, nodes 4-5 mm apart. +Fruits +: stalks 1-2 mm long, ca. 1 mm thick at base, covered with caducous stellate hairs; in life mature calyx red-brown, chartaceous, lobes 5, 2-3 larger than rest, attached to half inferior ovary, above forming a cup, glabrous outside, inner part at base completely covered with stellate hairs, lobes elliptic, apex rounded with 5 longitudinal prominent veins on the adaxial surface, 2.3-3.3 +x +0.5-0.8 cm; shorter lobes 0.8-1 +x +ca. 0.2 cm; nut ovoid, 5-6 mm diameter, with persistent stigma, densely covered with stellate hairs, half hidden within calyx. + + + +Distribution. +Endemic in Peninsular Malaysia, known only from Kelantan (Relai Forest Reserve, Gua Musang) and Pahang (Gua Tanggang, Merapoh). + + +Etymology. + +This species is named in honour of the Prime Minister of Malaysia, +Dato' +Sri Mohd Najib bin Tun Abdul Razak, for his strong interest in nature conservation and protection of the environment. + + + +Provisional conservation status. + +Endangered B2ab(iii). This species is known from the summit of two isolated karst limestone hills in Relai Forest Reserve, Gua Musang District, Kelantan and Gua Tanggang, Merapoh, Pahang, about 40 km apart ( +Liew et al. 2016 +). Together they have an area of occupancy of less than 10 km2 (Figure +3 +). The Relai Forest Reserve is classified as a permanent forest reserve but is currently threatened by encroachment by oil palm plantations that pose a high risk of burning to the limestone vegetation, as well as disturbance from ongoing logging in the Sungai Relai Forest Reserve. Gua Tanggang in Merapoh, on the other hand, is situated outside of Taman Negara which means that it is not in a protected area. + + + +Habitat. +It is an emergent tree on the rugged summit of karst limestone at 178-520 m altitude growing in rock fissures with a thick layer of leaf litter. + + +Phenology. +Fruiting specimens were collected in Relai Forest Reserve in October and Gua Tanggang in early August; complete flowers not seen but in October, many calyces and a few petals were collected. + + +Additional specimen examined. + +Peninsular Malaysia. Pahang, Lipis District, Merapoh, Gua Tanggang, +4.410000N +, +102.055000E +, 520 m alt., 6 August 1996, Saw et al. FRI 44774 (KEP!) + + + +Figure 3. +Distribution of + +Vatica najibiana + +in Peninsular Malaysia. + + + +
+
\ No newline at end of file diff --git a/data/38/D5/D4/38D5D4B9F02D544C91158FF813429B48.xml b/data/38/D5/D4/38D5D4B9F02D544C91158FF813429B48.xml new file mode 100644 index 00000000000..382057a8ac7 --- /dev/null +++ b/data/38/D5/D4/38D5D4B9F02D544C91158FF813429B48.xml @@ -0,0 +1,373 @@ + + + +A review of Apha floralis species group (Lepidoptera: Eupterotidae) + + + +Author + +Zolotuhin, Vadim V. +https://orcid.org/0000-0001-6403-7433 +Ulyanovsk State Pedagogical University, Lenin square 4 / 5, Ulyanovsk, 432071, Russia +v.zolot@mail.ru + + + +Author + +Pugaev, Sergey N. +Ulyanovsk State Pedagogical University, Lenin square 4 / 5, Ulyanovsk, 432071, Russia + + + +Author + +Du, Tran Thieu +Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet, Cay Giay, Hanoi, 100000, Vietnam + +text + + +Acta Biologica Sibirica + + +2020 + +2020-12-17 + + +6 + + +611 +635 + + + + +http://dx.doi.org/10.3897/abs.6.e59529 + +journal article +http://dx.doi.org/10.3897/abs.6.e59529 +2412-1908-6-611 +482EFF14668B4A2F94C2900541A2821E +9868B63A42C25237BA36D784CDB43606 + + + + +Apha floralis Butler, 1881 + + + + +Figs 1-4 + + + + +Apha floralis +Butler, 1881, Illustrations of typical specimens of +Lepidoptera +Heterocera +in the collection of the British Museum 5: 64, pl. XCIV, figs 5, 6. TL: "India, Darjeeling". Lectotype: male (BMNH), +here designated +[examined]. + + +Preptothauma oxydiata += +Preptothauma oxydiata +Draudt, 1931, Entomologische Rundschau 48(11): 121. TL: erroneously given as "West-Columbia, Altaquer, 500 m". Holotype: female (ZMHU) [examined]. + + + +Material examined. + +Lectotype +, + +, Darjiling, 79. 57 (BMNH). + +Paralectotype +, + +, +Darjiling +, 79. 57 (BMNH); f#, +Darjeeling +(ZMHU) + +; + + +, +India +, +Himalaya +, +Darj +[eeling], 15.X [19]18 (MWM) + +; + + +, +India +W.B., +Darjeeling +, + +2.000 m + +, +17-22.VII.1989 +, leg. +W. Thomas +(SMFL) + +; + + +, +Sikkim +, +Harmand +, 1890 (MNHN) + +; + +12 ♂♂ +, +Nepal +, +Annapurna Himal +, + +1.700 m + +, + +1 km +N of Tal + +, +84°23'E +, +28°28'N +, +08.VI.1996 +, leg. +Hreblay +& +Szaboky +(MWM) + +; + + +, +Nepal +Annapurna Himal +, + +2.450 m + +, +83°43'E +, +28°22'N +, +23-24.VI 1996 +, leg. +Gy. M. Lszl +& +G. Ronkay +(MWM) + +; + +2 ♂♂ +, +East-Nepal +, +Surke Danda +, + +3 km +NE Sukeyer + +, +Lali Kharka +18.V.1997 +, + +2.600 m + +, lg. +Hreblay +& +Szecsenyi +(MWM) + +; + +3 ♂♂ +, +East-Nepal +, +Deorali Danda +, +Anpan +, + +1.900 m + +, +18.VI.1998 +, leg. +M. Hreblay +& +B. Benedek +(MWM) + +; + +2 ♂♂ +, E. +Nepal +, +Janakpur +, +Dolakha Deolari +, + +2.800 m + +, +25.V.-7.VI.1994 +, +M. S. Limbu +leg. (NSMT) + +; + +14 ♂♂ +, +4 ♀♀ +, C. +Nepal +, Kali-Gandaki-Tal, +Kalopani-Dhumpu +, + +2.500 m + +, +30.V.-15.VI.1973 +, leg. +Dierl-Lehmann +(ZSM) + +. + + + +Description. + +Male +(Figs +1 +, +2 +). The forewing length is 25-29 mm. The costa is straight; the fore wing apex is weakly falcate. The wing pattern is contrasting, with yellow and bright brown (brick-red) colours predominating. Discal dot is always distinct, dark coloured and rounded. The antemedial fascia is brown to brick-red or light-brown, serrate. The outer field bordering the antemedial fascia can have duplicating serrate fasciae (from one to three). The postmedial fascia is straight, bright yellow in colour and has the distal margin extending to the apex. The fore wing apical patch is elongated, yellow or pale yellow. The postmedial fascia of the fore wing is fused with the distal part of the apical patch. It is bordered basally by a thin dark shadow which does not reach the wing apex, but is angled towards the costa. The submarginal fascia is zigzag-shaped, with expansion along the veins, terminating as a dark field at the wing apex. The postmedial fascia situated across the middle of the hind wing separates the outer yellow field of the wing from the inner brown one. The latter itself becoming more yellowish basally; submarginal fascia brown, zigzag-shaped, with corresponding separate dots on veins. + + +Male genitalia +(Figs +15 +, +16 +). Lobes of uncus are narrow, sabre-shaped with rounded apex, their bases fused at one third of their length. The valvae are roundly triangular; without saccular lobes but with three small spurs which are directed inwards (sometimes hardly visible depending on the preparation). The coecum is short, not longer than its width; the opening of vesica is usually more sclerotized. The vesica is dome-shaped, its base is completely covered with short cornuti which are poorly extended to the aedeagus tube. + + +Female +(Figs +3 +, +4 +). Length of the fore wing is 31 - 33 mm; similar in pattern to the male but is generally larger and paler. Additionally, the female is not so contrastingly coloured. The wings are wider with a more blunt apex and with vague basal fascia and light brown discal dot. The abdomen is light red laterally and terminally. + + +Female genitalia +(Figs +21-23 +). Ovipositor lobes are bean-shaped. Anterior apophyses are slender with well-marked, sclerotized base extending to the base of posterior apophyses which are a bit shorter. Postvaginal plate with acute margins and well-marked medio-caudal dent. Ostium is sheltered by the antevaginal plate which consists of two lobes laterally. Antrum is wide, calycine, slightly sclerotized, standing proud of antevaginal plate ventrally. Ductus bursae is not sclerotized, wide up to the curve and narrowing beyond that. A single thorn-shaped signum is situated at the equator of the corpus bursae, long, slightly curved, with broader base. + + + +Diagnosis. + +The males of the species differ from some of the other members of the group by having a well expressed +"double" +postmedial fascia on the hind wing. This +"double" +postmedial fascia can be also found in + +A. zephyrus + +and + +A. witti + +, but in both the latter species this fascia (not its basal shadow) is much more weakly expressed. The species + +A. floralis + +can be distinguished from + +A. zephyrus + +sp. nov. and + +A. witti + +sp. nov. by the smaller distance between the postmedial fascia and outer wing margin. Lobes of uncus are more slender and longer than in other species. Valvae with small apical spurs visible only under magnification. Aedeagus is straight in contrast to faintly curved in the other three species, cornuti on vesica are sparse, not dense as in other species. Saccus is small and not substantially distinguished. + + + +Distribution. + +Northern India and Nepal (Fig. +58 +). + + + +Bionomics. +Mountain species producing at least two generations per year with flight periods in June-July and October; it can be found at altitudes of 1.700 - 2.500 m. Preimaginal stages and host plants are unknown. + + +Taxonomic remarks. + +The species was described from a pair with a remark "Darjiling (Lidderdale & Sadler)". Both specimens are currently deposited in the BMNH and the male is specified as a lectotype. It completely matches the original description by Butler (1881: pl. XCIV, fig. 5) and has the following labels: yellowed rectangle with the inscription "Apha | floralis ♂| Butler, Type" and overleaf "Darjiling | 79.57"; a rectangular small label +"Darj." +; a circle with red framing and overprint +"Type" +. It is supplied with a standard red label with overprint "Eupterotidae | LECTOTYPE ♂ | Apha | floralis Butler, 1881 | Typical Spec. Lep. Het. | Brit. Mus. 5: 64. | des. S. Pugaev 2011". The syntypic female becomes therefore a paralectotype and is supplied with a corresponding red label. + + +Incorrect geographic label of Preptothauma oxydiata Draudt, 1931 (Fig. 4) was already discussed by Forbes (1955: 85) who stated "A fourth species described from western Colombia +... +agrees as figured so exactly with the east Asiatic A. subdives Butler that I am inclined to believe there has been an error in the locality". +Naessig +and Oberprieler (2008: 62-63) noted as well: +"... +Preptothauma oxydiata +... +, it evidently represents either A. subdives, A. floralisButler 1881 or a closely related species". The external characters and female genitalia of the taxon Preptothauma oxydiata unambiguously correspond to A. floralis and are well distinguished from the rest of the allied species; the synonymy of A. floralis and P. oxydiata was established by Becker (1996: 61). However, P. oxydiata is type species of the genus Preptothauma Draudt which therefore becomes a new synonym of Apha (this has not been stated by Becker), syn. nov. + + + + \ No newline at end of file diff --git a/data/38/D5/E3/38D5E3868CA8126915C65B214CF46B25.xml b/data/38/D5/E3/38D5E3868CA8126915C65B214CF46B25.xml new file mode 100644 index 00000000000..5c9940fc6f3 --- /dev/null +++ b/data/38/D5/E3/38D5E3868CA8126915C65B214CF46B25.xml @@ -0,0 +1,103 @@ + + + +Introduction of the Exocelina ekari-group with descriptions of 22 new species from New Guinea (Coleoptera, Dytiscidae, Copelatinae) + + + +Author + +Shaverdo, Helena V. + + + +Author + +Surbakti, Suriani + + + +Author + +Hendrich, Lars + + + +Author + +Balke, Michael + +text + + +ZooKeys + + +2012 + +250 + + +1 +76 + + + + +http://dx.doi.org/10.3897/zookeys.250.3715 + +journal article +http://dx.doi.org/10.3897/zookeys.250.3715 +1313-2970-250-1 + + + + +1. +Exocelina alexanderi Shaverdo, Hendrich & Balke +sp. n. +Figs 8A-E, 34 + + + +Type locality. +Indonesia: West Papua Province: Manokwari Regency, Arfak Mts., Tetaho area, Iranmeba. + + +Type material. +Holotype: male "IRIAN JAYA: Vogelkop Tetaho area, Iranmeba 1500-1700 m, 25.3.1993 leg. A. Riedel" (NHMW). Paratypes: 8 males, 6 females with the same label as the holotype, 1 male additionally with a green label "DNA M.Balke 3255" (NHMW, ZSM). 1 male "IRIAN JAYA: Vogelkop Testega-Meydoudga 1100 m, 4.4.1993 leg. A. Riedel" (NHMW). 1 male "Testegal / Iranmeba" [hw] (ZSM). + + +Diagnosis. +Beetle middle-sized, dark brown to piceous; pronotum with distinct lateral bead; male antennomeres 3 and 4 evidently larger than other, with external margin expanded (antennomeres triangular, elongated); male protarsomere 4 with small (only slightly larger than more laterally situated large seta), thin, slightly curved anterolateral hook; median lobe with strong submedian constriction in ventral view, apex of median lobe almost truncate in lateral view and broad in ventral view; paramere with notch on dorsal side and subdistal part short and small, with not numerous, relatively short, thick, and flattened setae. The species is well recognizable by the modified antennae of the males. + + +Description. +Size and shape: Beetle middle-sized (TL-H 3.9-4.05 mm, TL 4.35-4.5 mm, MW 2.1-2.2 mm), with oblong-oval habitus, broadest at elytral middle. Coloration: Dorsally dark brown to piceous, with paler (reddish) anterior margin and vertex of head, lateral sides of pronotum, and narrow bands along elytral suture; head appendages yellowish to reddish-brown, legs slightly darker (Fig. 34). + +Surface sculpture: Head with dense punctation (spaces between punctures 1-3 times size of punctures), evidently finer and sparser anteriorly; diameter of punctures smaller than diameter of cells of microreticulation. Pronotum with finer, sparser, and more evenly distributed punctation than on head. Elytra with very sparse and fine punctation, almost invisible. Head, pronotum, and elytra with strongly impressed microreticulation, dorsal surface shiny but duller than of +Exocelina oceai +sp. n. Head with microreticulation stronger. Metaventrite and metacoxa distinctly microreticulate, metacoxal plates with longitudinal strioles and transverse wrinkles. Abdominal sternites with distinct microreticulation, strioles, and fine sparse punctation, coarser and denser on two last abdominal sternites. + +Structures: Pronotum with distinct lateral bead. Base of prosternum and neck of prosternal process with distinct ridge, without anterolateral extensions. Blade of prosternal process lanceolate, narrow, convex, with distinct bead and few setae; neck and blade of prosternal process evenly jointed. Abdominal sternite 7 broadly rounded apically. +Male: Antennomeres 3-6 strongly enlarged, antennomeres 3 and 4 evidently larger than other, with external margin expanded (antennomeres triangular, elongated), 7-9 somewhat enlarged (Fig. 8A); antennomeres 3-7 rugose ventrally. Protarsomere 4 with small, thin, slightly curved anterolateral hook. Protarsomere 5 ventrally with anterior row of 14 short setae and posterior row of 7 short setae (Fig. 8B). Abdominal sternite 7 with 10-15 lateral striae on each side. Median lobe with strong submedian constriction in ventral view, apex of median lobe almost truncate in lateral view and broad in ventral view (Figs 8C, D). Paramere with notch on dorsal side and subdistal part short and small, with not numerous, relatively short, thick, and flattened setae (Fig. 8E). +Female: Antennae simple, abdominal sternite 7 without striae. + + +Distribution. + +Indonesia: West Papua Province: Manokwari Regency. This species is known from the eastern +Bird's +head only. Iranmeba and Testega are situated some 20-30 km west of Anggi-Lakes in the Arfak Mountains (Fig. 50). + + + +Etymology. + +The species is named for friend and most enthusiastic explorer of New +Guinea's +entomofauna, Alexander Riedel (Karlsruhe, Germany), who discovered this species. The species name is a noun in the genitive case. + + + + \ No newline at end of file diff --git a/data/38/D6/14/38D614283039F9C96B2930639F0F048A.xml b/data/38/D6/14/38D614283039F9C96B2930639F0F048A.xml new file mode 100644 index 00000000000..a7c2e176775 --- /dev/null +++ b/data/38/D6/14/38D614283039F9C96B2930639F0F048A.xml @@ -0,0 +1,181 @@ + + + +Order Rodentia - Family Cricetidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 2 + + + +955 +1189 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316535 + + + + + +Alticola (Aschizomys) macrotis +(Radde 1862) + + + + + + + +[Thomasomys] macrotis +Radde 1862 + +, + +Reise in den +Suden +von Ost-Sibierien, Vol. 1: 196 + + +. + + + + +Type Locality: + +Russia +, S Siberia, S +Krasnoyarsk Krai +, Vostochnyy Sayan Mtns. + + + + + +Vernacular Names: +Large-eared Mountain Vole +. + + + + +Synonyms: + +Alticola (Aschizomys) altaica +Vinogadov 1933 + +; + +Alticola (Aschizomys) fetisovi +Galkina and Epifantseva 1988 + +; + +Alticola (Aschizomys) vinogradovi +Rasorenova 1933 + +. + + + + +Distribution: +Altai +of extreme NW +Xinjiang +and S Siberia, eastward through Tuvinskaya ( +Tuva region +) and Sayan Mtns, to highlands in Lake Baikal region. + + + + +Conservation: +IUCN +– Lower Risk (lc). + + + + +Discussion: +Subgenus + +Aschizomys + +. Closely related to the northern + +A. lemminus + +(see above), and either not allocated to subgenus ( +Ellerman, 1941 +), placed it in the subgenus + +Alticola +( +Ognev, 1964 +) + +, or considered under the subgenus + +Aschizomys + +( +Gromov and Erbajeva, 1995 +; +Gromov and Polyakov, 1977 +; +Pavlinov and Rossolimo, 1987 +). +Galkina and Epifantseva (1988) +described + +fetisovi + +as species, but others have included it in + +A. macrotis + +or considered its status unclear (Vasil’eva, 1999); + +Pavlinov et al. (1995 +a +) + +and +Pavlinov and Rossolimo (1998) +persuasively treated + +fetisovi + +as a synonym. Chromosomal variation reported by +Bolshakov et al. (1985) +. + + + + \ No newline at end of file diff --git a/data/38/D6/39/38D639EDB67BA1CDAAD1D3B6FF8702FB.xml b/data/38/D6/39/38D639EDB67BA1CDAAD1D3B6FF8702FB.xml new file mode 100644 index 00000000000..e0679ca518d --- /dev/null +++ b/data/38/D6/39/38D639EDB67BA1CDAAD1D3B6FF8702FB.xml @@ -0,0 +1,230 @@ + + + +Scarabaeinae dung beetles from Ecuador: a catalog, nomenclatural acts, and distribution records + + + +Author + +Chamorro, William + + + +Author + +Marin-Armijos, Diego + + + +Author + +senjo, Angelico + + + +Author + +Vaz-De-Mello, Fernando Z. + +text + + +ZooKeys + + +2019 + +826 + + +1 +343 + + + + +http://dx.doi.org/10.3897/zookeys.826.26488 + +journal article +http://dx.doi.org/10.3897/zookeys.826.26488 +1313-2970-826-1 +B1550A3AE54744509A44BC4366D5E110 + + + + +Phanaeus (Notiophanaeus) bispinus Bates, 1868 +Plate 46B + + + + +Phanaeus bispinus +Bates, 1868: 89 (original description. Type locality: Pastaza, Canelos). + + +Phanaeus bispinus +: +Gemminger and Harold 1869 +: 1017 (catalog); +Nevinson 1892 +: 2 (catalog, distribution); +Gillet 1911a +: 81 (catalog, distribution); +d' +Olsoufieff 1924 +: 34 (characters in key); 84 (redescription), 147 (distribution); +Blackwelder 1944 +: 209 (list of species from Latin America); +Vulcano and Pereira 1967 +: 574 (characters in key); +Arnaud 1982a +: 114 (list of the types of the MNHN); +Vitolo 2000 +: 597 (characters in key); +Medina et al. 2001 +: 140 (cited for Colombia); +Hamel-Leigue et al. 2006 +: 17 (list of species for Bolivia); +Krajcik 2012 +: 204 (complete list of species); +Ratcliffe et al. 2015 +: 197 (cited for Peru). + + +Phanaeus (Notiophanaeus) bispinus +: +Edmonds 1994 +: 33 (characters in key), 35 (redescription), 100 (distribution); +Vaz-de-Mello 2000 +: 194 (cited for Brazil); +Arnaud 2002a +: 89 (diagnosis); +Vitolo 2004 +: 283 (diagnosis); +Hamel-Leigue et al. 2009 +: 66 (distributional records from Bolivia); +Carvajal et al. 2011 +: 320-321 (cited for Ecuador); + +Edmonds and +Zidek +2012 + +: 9 (characters in key); +Figueroa et al. 2014 +: 133 (distributional records from Peru); +Boilly et al. 2016 +: 90 (characters in key); 93 (figures 19a, 19b and 19c); 96 (cited for Guyana); +Chamorro et al. 2018 +: 97 (cited for Ecuador). + + +Phanaeus digitalis +d'Olsoufieff +, 1924: 34 (original description); +Blackwelder 1944 +: 209 (list of species from Latin America); + +Pereira and +Martinez +1956b + +: 237 (synonym of +Phanaeus bispinus +Bates, 1868); +Frey 1963 +: 559 (cited as synonym of +Phanaeus bispinus +Bates, 1868); +Edmonds 1994 +: 35 (synonym of +Phanaeus bispinus +Bates, 1868); +Arnaud 2002a +: 89 (synonym of +Phanaeus bispinus +Bates, 1868); +Vitolo 2004 +: 283 (synonym of +Phanaeus bispinus +Bates, 1868); +Hamel-Leigue et al. 2009 +: 66 (synonym of +Phanaeus bispinus +Bates, 1868); + +Edmonds and +Zidek +2012 + +: 5 (junior synonym of +Phanaeus bispinus +Bates, 1868); +Figueroa et al. 2014 +: 133 (synonym of +Phanaeus bispinus +Bates, 1868). + + + +Type specimens. + +Phanaeus bispinus +Bates, 1868. The holotype (♂) is deposited at the MNHN (see +Edmonds 1994 +: 35). Locality: Canelos, Ecuador, not examined. + + +Phanaeus digitalis +d'Olsoufieff +, 1924. The holotype (♀) is deposited at the MNHN (see +Edmonds 1994 +: 35). Locality: Guyana, not examined. + + + +Distribution. +Bolivia, Brazil, Colombia, Ecuador, French Guiana, Guyana, Peru, and Venezuela. + + +Records examined. + +NAPO: Puerto Napo, 480 m (2 specimens MECN). ORELLANA: +Anangu +(1 specimen MQCAZ); Dayuma Campo Palanda, plataforma Primavera 1, 235 m (6 specimens MUTPL); Dayuma Campo Pindo, plataforma Pindo Este 1, 305 m (1 specimen MUTPL); Onkone Gare, 220 m, Parque Nacional +Yasuni +(1 specimen MUTPL); El Coca, plataforma Oso B (1 specimen MUTPL); Yasuni Puce BS, 200 m, +Rio +Tiputini (3 specimens MQCAZ). +SUCUMBIOS +: Garzacocha (1 specimen MQCAZ); Tarapoa, 260 m, Fanny 5 (1 specimen MUTPL); Tarapoa, Nuevo +Manabi +, 270 m (1 specimen MUTPL). + + + +Literature records. + +NAPO: Tena, 400 m ( +Edmonds 1994 +: 100); without specific locality ( +Arnaud 2002a +: 89). PASTAZA: Canelos ( +Bates 1868 +: 89; +Edmonds 1994 +: 100). + + + +Temporal data. +Collected in February, May, August, September, October, and November. + + +Remarks. +Inhabits the lowland evergreen forests of the Amazon region from 220-400 m a.s.l. Collected manually and with pitfall traps baited with human feces. + + + \ No newline at end of file diff --git a/data/38/D7/21/38D721C0B6D1BBDBE45B9FA2F038ED04.xml b/data/38/D7/21/38D721C0B6D1BBDBE45B9FA2F038ED04.xml new file mode 100644 index 00000000000..0a29f85e297 --- /dev/null +++ b/data/38/D7/21/38D721C0B6D1BBDBE45B9FA2F038ED04.xml @@ -0,0 +1,126 @@ + + + +The beetle fauna (Insecta, Coleoptera) of the Rawdhat Khorim National Park, Central Saudi Arabia + + + +Author + +Abdel-Dayem, Mahmoud S. +https://orcid.org/0000-0002-6276-1740 +King Saud University Museum of Arthropods (KSMA), Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, P. O. Box 2460 Riyadh 11451, Saudi Arabia +mseleem@ksu.edu.sa + + + +Author + +Fad, Hassan H. +Entomology Department, Faculty of Science, Ain Shams University, Cairo, Egypt + + + +Author + +El-Torkey, Ashraf M. +Plant Protection Research Institute, Agriculture Research Center, Giza, Egypt + + + +Author + +Elgharbawy, Ali A. +King Saud University Museum of Arthropods (KSMA), Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, P. O. Box 2460 Riyadh 11451, Saudi Arabia & Zoology Department, Faculty of Science, Al Azhar University, Nasr City, Cairo, Egypt + + + +Author + +Aldryhim, Yousif N. +King Saud University Museum of Arthropods (KSMA), Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, P. O. Box 2460 Riyadh 11451, Saudi Arabia + + + +Author + +Kondratieff, Boris C. +Department of Bioagricultural Sciences and Pest Management, Colorado State University, Campus Delivery 1177, Fort Collins, Colorado, U. S. A. 80523 + + + +Author + +Ansi, Amin N. Al +King Saud University Museum of Arthropods (KSMA), Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, P. O. Box 2460 Riyadh 11451, Saudi Arabia + + + +Author + +Aldhafer, Hathal M. +King Saud University Museum of Arthropods (KSMA), Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, P. O. Box 2460 Riyadh 11451, Saudi Arabia + +text + + +ZooKeys + + +2017 + +2017-02-07 + + +653 + + +1 +78 + + + + +http://dx.doi.org/10.3897/zookeys.653.10252 + +journal article +http://dx.doi.org/10.3897/zookeys.653.10252 +1313-2970-653-1 +8ECC0674017A48588BE8DDD05C0D7CF6 +FFE87C63852C5772725FBE55FF95902D +269679 + + + + +Tillodenops plagiatus (Fairmaire, 1892) + + + +World distribution. + +Africa +: KE, MR, SD, SN, SO, TZ. +Asia +: AE, IR, OM, SA, YE. The distribution is updated from +Gerstmeier (2010) + + + +General distribution. +AFR_SAR. + + +Local distribution. + +AS, BA, JZ, MD, MK ( +Menier 1986 +). + + + +Collecting month and method. +Very rare species, which was collected by LT during IV and X. + + + \ No newline at end of file diff --git a/data/38/D7/F3/38D7F3551FFFC957A1E0A3AD7E98C2F1.xml b/data/38/D7/F3/38D7F3551FFFC957A1E0A3AD7E98C2F1.xml new file mode 100644 index 00000000000..49e24a54fe1 --- /dev/null +++ b/data/38/D7/F3/38D7F3551FFFC957A1E0A3AD7E98C2F1.xml @@ -0,0 +1,87 @@ + + + +Faunistic diversity of spiders (Araneae) in Galichitsa mountain (FYR Macedonia) + + + +Author + +Deltshev, Christo + + + +Author + +Komnenov, Marjan + + + +Author + +Blagoev, Gergin + + + +Author + +Georgiev, Teodor + + + +Author + +Lazarov, Stoyan + + + +Author + +Stojkoska, Emilija + + + +Author + +Naumova, Maria + +text + + +Biodiversity Data Journal + + +2013 + +1 + + +977 +977 + + + + +http://dx.doi.org/10.3897/BDJ.1.e977 + +journal article +http://dx.doi.org/10.3897/BDJ.1.e977 +1314-2828--977 + + + + +SALTICIDAE +Araneae +Arachnida +Arthropoda +Animalia + + + + +SALTICIDAE + + + + \ No newline at end of file diff --git a/data/38/D9/08/38D90801FCBA51A9966A311F352381C2.xml b/data/38/D9/08/38D90801FCBA51A9966A311F352381C2.xml new file mode 100644 index 00000000000..a9db5475751 --- /dev/null +++ b/data/38/D9/08/38D90801FCBA51A9966A311F352381C2.xml @@ -0,0 +1,324 @@ + + + +Two new species of Cymodusa Holmgren (Hymenoptera, Ichneumonidae) with a key to species known from China and Oriental region + + + +Author + +Li, Tao +General Station of Forest and Grassland Pest Management, National Forestry and Grassland Administration, Shenyang 110034, China + + + +Author + +Chang, Guo-Bin +General Station of Forest and Grassland Pest Management, National Forestry and Grassland Administration, Shenyang 110034, China + + + +Author + +Yang, Zai-Hua +Guizhou Academy of Forestry, Guiyang, Guizhou, 550005, China + + + +Author + +Sun, Shu-Ping +General Station of Forest and Grassland Pest Management, National Forestry and Grassland Administration, Shenyang 110034, China + + + +Author + +Tian, Yue +Fanjingshan National Natural Reserve Administration, Jiangkou, Guizhou 554400, China + + + +Author + +Sheng, Mao-Ling +https://orcid.org/0000-0003-0141-4697 +General Station of Forest and Grassland Pest Management, National Forestry and Grassland Administration, Shenyang 110034, China +shengmaoling@163.com + +text + + +Journal of Hymenoptera Research + + +2021 + +2021-12-30 + + +88 + + +103 +114 + + + + +http://dx.doi.org/10.3897/jhr.88.75304 + +journal article +http://dx.doi.org/10.3897/jhr.88.75304 +1314-2607-88-103 +C7C29787CD5743B0BC1D02DF5B13B12D +D47B10384BC252F1A58F60722098E5F9 +5826613 + + + + + +Cymodusa melana Sheng, Li & Sun +sp.nov. + + + + +Figures 10-14 +, 15-20 + + + +Diagnosis. + +Dorsal median portion of occipital carina (Fig. +14 +) angled. Anterior tentorial pit distinct, against eye. Postocellar line approximately 1.2 +x +as long as ocular-ocellar line. Lateral carinae of area basalis almost parallel, 1.2-1.3 +x +as long as wide. Lateromedian longitudinal carinae distinctly angled in level of posterior transverse carina. Tergites 2 (Fig. +19 +) elongate, 1.7-1.8 +x +as long as posterior width. Posteromedian portions of tergites 6-7 (Fig. +20 +) distinctly concave. Head, mesosoma, all metasomal tergites and hind leg almost entirely black. + + + +Figures 10-14. + +Cymodusa melana + +Sheng, Li & Sun, sp.nov. Holotype. Female +10 +habitus, lateral view +11 +head, anterior view +12 +head, dorsal view +13 +head and pronotum, lateral view +14 +head, dorsoposterior view. + + + + +Description. +Body length 7.0-7.5 mm. Fore wing length 3.5-4.0 mm. Ovipositor sheath 1.2-1.5 mm. + + +Head +. + +Eye with weak, short setae, inner margins (Fig. +11 +) distinctly concave near antennal sockets. Face and clypeus roughly shagreened. Face strongly convergent ventrally, maximum width beneath antennal socket approximately 1.8 +x +as long as minimum width, dorsal margin concave medially. Clypeus with dense fine punctures, evenly convex, apical margin evenly convex forward. Anterior tentorial pit small, distinct, against eye. Mandible with dense yellowish white setae and sparse fine punctures; lower tooth almost as long as upper tooth. Malar space about 0.1 +x +as long as basal width of mandible. Gena (Figs +12 +, +13 +, +14 +) shagreened, lower portion with dense delicate yellowish white setae, upper portion strongly convergent backward. Vertex finely shagreened, posterior portion behind hind margin of stemmaticum steeply oblique. Postocellar line approximately 1.2 +x +as long as ocular-ocellar line. Frons almost flat, shagreened, median portion with fine indistinct transverse wrinkles. Antenna with 32 flagellomeres; ratio of length from first to fifth flagellomeres: 2.0:1.3:1.2:1.2:1.1. Occipital carina (Fig. +14 +) complete, dorsal median portion angulated. + + + +Figures 15-20. + +Cymodusa melana + +Sheng, Li & Sun, sp. nov. Holotype. Female +15 +mesoscutum and scutellum, dorsal view +16 +mesosoma, lateral view +17 +propodeum, dorsal view +18 +first tergite, lateral view +19 +postpetiole and tergite 2, dorsal view +20 +(Paratype) Posterior portion of metasoma, dorsal view. + + + + +Mesosoma +. + +Lateral concavity of pronotum (Figs +13 +, +16 +) with dense strong oblique wrinkles; dorsoposterior portion roughly shagreened. Epomia long and strong. Mesoscutum (Fig. +15 +) evenly convex, with leathery texture, lateral portion with fine distinct punctures, distance between punctures 0.2-1.5 +x +as long as one diameter of puncture; posterior portion with short indistinct transverse wrinkles. Notaulus indistinct. Scuto-scutellar groove with 6-7 distinct longitudinal carinae. Scutellum finely shagreened, basal 0.25 with lateral carina. Postscutellum transversely convex, anterior portion depressed transversely, anterolateral with small pit. Lower half of mesopleuron (Fig. +16 +) slightly convex; median portion in front of speculum with distinct oblique wrinkles; beneath subtegular ridge with short indistinct transverse wrinkles. Speculum almost smooth, shining. Epicnemial carina strong, upper end almost reaching front edge of mesopleuron, about 0.7 distance to subtegular ridge. Metapleuron evenly convex, with dense grayish white setae; juxtacoxal carina absent; submetapleural carina complete. Hind femur 5.7-6.0 +x +as long as its maximum width. Ratio of length of hind tarsomeres from first to fifth: 5.5:2.7:1.7:1.0:1.0. First tarsomere 2.4 +x +as long as length of longer spur. Claw small, pectinate basally. Wings slightly brownish, hyaline. Fore wing with vein 1cu-a slightly basal of M&RS. Areolet sessile, receiving vein 2m-cu approximately at middle, 2rs-m approximately as long as 3rs-m; postnervulus intercepted at middle. Hind wing with basal portion of M+CU distinctly arched; nervellus almost vertical, intercepted at lower 0.25; final abscissa of CU unpigmented. Propodeum (Fig. +17 +) roughly shagreened, lateral portion with dense gray setae; lateromedian longitudinal carinae strong, distinctly angled in level of posterior transverse carina; area basalis separated from area superomedia by weak carina, lateral sides slightly convergent anteriorly or parallel, 1.6-1.7 +x +as long as anterior width, 1.2-1.3 +x +as long as posterior width; areas superomedia slightly wider than long; areas superomedia and petiolaris completely confluent, with short, indistinct transverse wrinkles; costula present. Propodeal spiracle small, circular. + + + +Metasoma +. + +First tergite (Fig. +18 +) 3.2 +x +as long as apical width; petiole smooth, shiny, lateral side slightly longitudinally concave; postpetiole (Fig. +19 +) distinctly convex, shagreened; spiracle small, weakly convex, located approximately at apical 0.35. Tergites 2 (Fig. +19 +) with texture as postpetiole, elongate, slightly evenly widened posteriorly, 1.7-1.8 +x +as long as posterior width. Tergite 3 with parallel sides, 1.3 +x +as long as posterior width. Fourth and subsequent tergites compressed. Posteromedian portions of tergites 6-7 (Fig. +20 +) distinctly concave. Ovipositor sheath 1.2 +x +as long as hind tibia. Apical portion of ovipositor weakly compressed, with sharp dorsal notch. + + +Coloration +(Fig. +10 +). Black, except for the following: ventral profile of base of antenna reddish brown. Mandible except teeth, maxillary palpi, labial palpi yellow. Tegula, fore and middle legs reddish brown, except coxae black and ventral profiles of trochanters darkish brown. Hind trochantellus yellow. Base of hind femur reddish brown. Pterostigma and veins blackish brown. + + + +Etymology. +The specific name is derived from the body and hind leg almost entirely black. + + +Material examined. + + + +Holotype + +: +China +• + +; +Guizhou +, +Lengjiaba +, + +840 m + +, +Fanjingshan National Natural Reserve +, +Jiangkou +; +24.VI.2019 +; IT by Zhen-Hai Yang + +. + + +Paratypes + +: +China +• +1♀ +; same data as for holotype. • +1♀ +; same data as for +holotype +except +23.IX.2019 + +. + +China +• +2♀♀ +; +Guizhou +, +Panlongshan +, + +1179 m + +, Wudang, Guiyang; +24.VI.2019 + +; IT by Zai-Hua Yang. + + + +Distribution. +China. + + +Differential diagnosis. + +The new species is similar to + +C. taprobanica + +(Cameron, 1905), but can be distinguished from the latter by the following combination of characters: areolet sessile; area basalis of propodeum at most 1.7 +x +as long as maximum width; area superomedia wider than length; hind leg almost entirely black. + +Cymodusa taprobanica + +(Cameron): areolet petiolate; area basalis of propodeum about 3.0 +x +as long as wide; area superomedia longer than width; hind leg partly black. + + + + + \ No newline at end of file diff --git a/data/38/D9/0B/38D90B6AA4C35C39F559644A55CB241A.xml b/data/38/D9/0B/38D90B6AA4C35C39F559644A55CB241A.xml new file mode 100644 index 00000000000..f9cabd9b5a5 --- /dev/null +++ b/data/38/D9/0B/38D90B6AA4C35C39F559644A55CB241A.xml @@ -0,0 +1,81 @@ + + + +An annotated checklist of the scale insects of Iran (Hemiptera, Sternorrhyncha, Coccoidea) with new records and distribution data + + + +Author + +Moghaddam, Masumeh + +text + + +ZooKeys + + +2013 + +334 + + +1 +92 + + + + +http://dx.doi.org/10.3897/zookeys.334.5818 + +journal article +http://dx.doi.org/10.3897/zookeys.334.5818 +1313-2970-334-1 + + + + +Ceroplastes rusci (Linnaeus) + + + + +Coccus rusci +Linnaeus, 1758: 456. + + + +Iran localities. +Fars, Kohgilouyeh & Boyerahmad, Lorestan, Sistan & Balouchestan. + + +Host plants. + +Moraceae +: +Ficus carica +. + + + +References. + +Ben-Dov et al. (2013) +, +Farahbakhsh (1961) +, +Kaussari (1946a) +, + +Kozar +et al. (1996) + +, +Moghaddam (2009) +and +Moghaddam and Tavakoli (2010) +. + + + + \ No newline at end of file diff --git a/data/38/D9/2C/38D92CD0438683BAFE7889960297E4A5.xml b/data/38/D9/2C/38D92CD0438683BAFE7889960297E4A5.xml new file mode 100644 index 00000000000..86096a8ed6b --- /dev/null +++ b/data/38/D9/2C/38D92CD0438683BAFE7889960297E4A5.xml @@ -0,0 +1,127 @@ + + + +The Mecyclothorax beetles (Coleoptera, Carabidae, Moriomorphini) of Haleakala-, Maui: Keystone of a hyperdiverse Hawaiian radiation + + + +Author + +Liebherr, James K. + +text + + +ZooKeys + + +2015 + +544 + + +1 +407 + + + + +http://dx.doi.org/10.3897/zookeys.544.6074 + +journal article +http://dx.doi.org/10.3897/zookeys.544.6074 +1313-2970-544-1 +C5978BD0145B40F8ACDEB27371B7B9A4 +C5978BD0145B40F8ACDEB27371B7B9A4 + + + +Taxon classification Animalia Coleoptera Carabidae + + + +(030) +Mecyclothorax anthracinus +sp. n. +Figs 44E, 45 +F-G +, 46B, 47B, 48 + + + +Diagnosis. +The small, dark-bodied beetles that comprise this species look ever so like small bits of anthracite coal, their dorsal body surface a reflective black (Fig. 44E). Also, this is the only species in the group that is characterized by absence of the parascutellar seta. The pronotum is narrow and basally constricted, MPW/PL = 1.18-1.24, MPW/BPW = 1.42-1.50, the disc covered with well-developed transverse wrinkles. The elytral intervals are convex and striation irregular, with striae 5 and 6 fused near the basal groove, and the dorsal setal impressions foveate and of diameter equal to the width of interval 3, these impressions associated with longitudinal irregularities of striae 2 and 3. The femora are flavous apically and covered with a piceous cast over their basal third; tibiae piceous. Setal formula 2 2 2 2. Standardized body length 3.6-4.0. + + +Description + +(n = 5). Head capsule with frontal grooves deep near clypeus, straight with external carina to anterior supraorbital seta; dorsal surface of neck convex, eyes moderately convex, ocular ratio = 1.42-1.50, ocular lobe ratio 0.77-0.85; labral anterior margin broadly, shallowly emarginate, antennae filiform, antennomere 3 with sparse pelage of short setae; mentum tooth with orthogonal sides, apex pointed. Pronotum with lateral margin subparallel to convergent anterad right to acute hind angle; +median +base depressed relative to disc, covered with rugose wrinkles; basal margin nearly straight, slightly convex medially; median longitudinal impression shallow, finely incised, crossed by wrinkles; anterior transverse impression broad, evident, bordered anteriorly by slightly convex anterior callosity that is crossed by fine wrinkles; front angles slightly projected, rounded; anterior width subequal to broader than basal width, APW/BPW = 1.00-1.06; lateral marginal depression moderately narrow, edge upturned to beaded; laterobasal depression broad, depressed with wrinkled surface. Proepisternum with 6 minute punctures along hind marginal groove; prosternal process +medially +depressed, without marginal bead. Elytra subellipsoid, disc flat, sides moderately sloped; basal groove slightly recurved to tightly rounded humeral angle; humeri narrow, MEW/HuW = 2.06-2.10; parascutellar striole finely incised, continuous; sutural interval moderately convex, slightly more upraised than intervals 2-4; sutural and 2nd striae of subequal depth from base to apex; discal striae 1-8 complete and deep to apex, smooth with minute irregularities along striae suggesting punctulae; 7th and 8th intervals of similar convexity mesad subapical sinuation; 2 dorsal elytral setae at 0.32 +x +and 0.65 +-0.73x +elytral length; apical and subapical setae present; lateral elytral setae arranged in anterior series of 7 setae and posterior series of 4(5) setae; elytral marginal depression narrow, edge upturned; subapical sinuation very shallow, nearly obsolete. Mesepisternum with 8 shallow punctures in 2 rows; metepisternal width to length ratio = 0.71; metepisternum/metepimeron suture distinct, metathoracic flight wing an ovoid flap, length 2.5 +x +breadth, with reduced R and M veins, the flap extended 2/3 distance to hind margin of metanotum. Abdomen with indistinct lateral wrinkles on ventrites 1-3; suture between ventrites 2 and 3 complete; apical male ventrite with 2 marginal setae, apical female ventrite with 4 equally spaced marginal setae and a median trapezoid of 4, subequal short setae. Legs-metatarsomere 1/metatibial length ratio = 0.17; metatarsomere 4 length along outer lobe 1.2 +x +medial tarsomere length, apical and subapical setae present; metatarsal dorsolateral sulci broad, shallow. Microsculpture of vertex of granulate isodiametric sculpticells; pronotal disc covered with distinct transverse mesh, median base with granulate isodiametric sculpticells; elytral disc covered with well-developed transverse mesh, apex with well-developed isodiametric mesh in transverse rows; metasternum with upraised transverse mesh; laterobasal abdominal ventrites with swirling isodiametric and transverse microsculpture. Coloration of vertex granulate rufopiceous; antennomere 1 flavous, antennomeres 2-3 with piceous cast, 4-11 piceous; pronotal disc granulate rufopiceous, margins narrowly paler, rufobrunneous; proepipleuron rufobrunneous with piceous upper margin, proepisternum rufobrunneous with piceous cast; elytral disc rufopiceous, sutural interval paler, dark rufous throughout, margins narrowly paler basally, concolorous with disc apically; elytral epipleuron rufobrunneous, metepisternum rufopiceous; abdomen rufopiceous across width of ventrites 1-5, apical ventrite 6 with apical 1/3 paler, rufobrunneous. + + +Male genitalia (n = 1). Aedeagal median lobe curved, gracile, distance from parameral articulation to tip 4 +x +depth at midlength (Fig. 45F); apex angularly narrowed to tightly rounded tip formed at juncture of flat apical face and ventral margin; median lobe sinuously recurved left then right in ventral view (Fig. 45G), tip tightly rounded; internal sac with apparent dorsal ostial microtrichial patch (based on uneverted specimen; Fig. 45F), sac surface covered with microspicules; flagellar plate evident just inside dorsal margin of median lobe. + + +Female reproductive tract (n = 1). Bursa copulatrix a narrow digitiform lobe attached to broader vagina, lobe length 0.26 mm, lobe apical breadth 0.10 mm, vagina breadth 0.25 mm (Fig. 46B); bursal walls thin, transparent; gonocoxite 1 with 3 apical fringe setae and 5-6 smaller setae on medial surface (Fig. 47B); gonocoxite 2 falcate, +narrow +apically with base broadly extended laterally, 2 lateral ensiform setae with apical seta broader and longer, apical nematiform setae on medial surface at 0.75 +x +gonocoxite length. + + + +Holotype. + +Female (BPBM) labeled: NW 6000'-6500', / Haleakala / VIII-18-37 Maui // Beating // ECZimmerman / Collector // 3 // HOLOTYPE / +Mecyclothorax +/ +anthracinus +/ Liebherr / det. J.K. Liebherr 2015 (black-margined red label). + + + +Paratypes. + +HI: Maui: Haleakala N.P., NW upper slope, beating 1830-1980 m el., 18-viii-1937, Zimmerman (BPBM, 2); Koolau For. Res., Hanawi N.A.R., Frisbee Meadow Camp, woods below, sift litter +Dubautia +/tree, 2072-2099 m el., 19-v-1993 lot 01, Liebherr/Medeiros (CUIC, 6). + + + +Etymology. + +The shiny coal black color of the dorsal surface of these beetles begs for use of the Latin adjective +anthracinus +. + + + +Distribution and habitat. + +Mecyclothorax anthracinus +is known from two isolated, high-elevation localities near the upper limits of the windward forest. E.C. Zimmerman beat three specimens from vegetation at 1830-1980 m elevation along the NW upper slope, and six specimens were taken from leaf litter samples of +Dubautia reticulata +litter at "Frisbee Meadow Camp" in the headwaters of +Hanawī +Stream to the east (Fig. 48). Whether the unusual coal-black color and ridged dorsal body surface of +Mecyclothorax anthracinus +beetles serve to enhance crypsis on the dark, fissured bark of the tree +Dubautia +seems a question worthy of study. + + + + \ No newline at end of file diff --git a/data/38/D9/63/38D96323690518D5B13D4F620B5C5941.xml b/data/38/D9/63/38D96323690518D5B13D4F620B5C5941.xml new file mode 100644 index 00000000000..700ccbb16a1 --- /dev/null +++ b/data/38/D9/63/38D96323690518D5B13D4F620B5C5941.xml @@ -0,0 +1,144 @@ + + + +The beetle fauna (Insecta, Coleoptera) of the Rawdhat Khorim National Park, Central Saudi Arabia + + + +Author + +Abdel-Dayem, Mahmoud S. +https://orcid.org/0000-0002-6276-1740 +King Saud University Museum of Arthropods (KSMA), Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, P. O. Box 2460 Riyadh 11451, Saudi Arabia +mseleem@ksu.edu.sa + + + +Author + +Fad, Hassan H. +Entomology Department, Faculty of Science, Ain Shams University, Cairo, Egypt + + + +Author + +El-Torkey, Ashraf M. +Plant Protection Research Institute, Agriculture Research Center, Giza, Egypt + + + +Author + +Elgharbawy, Ali A. +King Saud University Museum of Arthropods (KSMA), Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, P. O. Box 2460 Riyadh 11451, Saudi Arabia & Zoology Department, Faculty of Science, Al Azhar University, Nasr City, Cairo, Egypt + + + +Author + +Aldryhim, Yousif N. +King Saud University Museum of Arthropods (KSMA), Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, P. O. Box 2460 Riyadh 11451, Saudi Arabia + + + +Author + +Kondratieff, Boris C. +Department of Bioagricultural Sciences and Pest Management, Colorado State University, Campus Delivery 1177, Fort Collins, Colorado, U. S. A. 80523 + + + +Author + +Ansi, Amin N. Al +King Saud University Museum of Arthropods (KSMA), Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, P. O. Box 2460 Riyadh 11451, Saudi Arabia + + + +Author + +Aldhafer, Hathal M. +King Saud University Museum of Arthropods (KSMA), Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, P. O. Box 2460 Riyadh 11451, Saudi Arabia + +text + + +ZooKeys + + +2017 + +2017-02-07 + + +653 + + +1 +78 + + + + +http://dx.doi.org/10.3897/zookeys.653.10252 + +journal article +http://dx.doi.org/10.3897/zookeys.653.10252 +1313-2970-653-1 +8ECC0674017A48588BE8DDD05C0D7CF6 +FFE87C63852C5772725FBE55FF95902D +269679 + + + + +Agrilus desertus (Klug, 1829) + + + +World distribution. + +Africa +: MR, SO, TD. +Asia +: IL, IR, JO, SA, YE. +North Africa +: DZ, EG, LY, MA, TN. + + + +General distribution. +AFR_SAR. + + +Local distribution. + +AS ( + +Bily +1982 + +). + + + +Collecting month and method. + +A rare species. The specimens were collected by BV on branches of + +Acacia ehrenbergiana + +, + +Acacia gerrardii + +and + +Lycium shawii + +, and HP during IV-V, VIII and X. + + + + \ No newline at end of file diff --git a/data/38/DA/29/38DA29F17B5E63DFF8BFF992286DB5FF.xml b/data/38/DA/29/38DA29F17B5E63DFF8BFF992286DB5FF.xml new file mode 100644 index 00000000000..2a15f97cfc2 --- /dev/null +++ b/data/38/DA/29/38DA29F17B5E63DFF8BFF992286DB5FF.xml @@ -0,0 +1,607 @@ + + + +Info Flora Schweiz - Poaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/poaceae.html + +url + + + + + +Bromus sterilis +L. + + + + + +Taube Trespe + + + + +Art ISFS: 67200 Checklist: 1007540 +Poaceae +Bromus +Bromus sterilis L. + + + +Bestimmungsschluessel + + + +Zusammenfassung + + + + +Artbeschreibung + +(nach +Lauber & al. 2018 +) + +: +20-80 cm +hoch. +Blaetter +3-5 mm +breit, flaumig behaart. +Blatthaeutchen +2-4 mm +, lang gefranst. + +Rispe +15-25 cm +lang, allseitswendig, locker + +. +Aeste +schief aufrecht bis +ueberhaengend +, rau, +5-10 cm +lang, + +meist nur mit 1-2 +Aehrchen + +, die untersten mit mehreren +grundstaendigen +Zweigen. +Aehrchen +ohne die Grannen 2-3,5 cm lang. Deckspelze +15-22 mm +, ihre Granne +15-30 mm +lang. Spelzen kahl oder kurz borstig. Untere +Huellspelze +1-, obere 3nervig. + + + + +Bluetezeit + +(nach +Lauber & al. 2018 +) + +: 5-7 + + +Standort und Verbreitung in der Schweiz + +(nach +Lauber & al. 2018 +) + +: Unbebaute Orte, +Wegraender +/ kollin-montan(-subalpin) / CH + + + + +Verbreitung global + +(nach +Lauber & al. 2018 +) + +: Eurasiatisch + + + + +Oekologische +Zeigerwerte + +(nach +Landolt & al. 2010 +) + +234-344.t.2n=14(28) + + + +Status + + + +Status IUCN +: Nicht +gefaehrdet + + + +Anatomie + +Zusammenfassung +der Blattanatomie Obere Epidermiszellen gleich gross wie untere. Verbindungs-Steg zwischen oberer und unterer Epidermis homogen verholzt. +Leitbuendel +im Verbindungs-Steg in der Mitte eingebettet. +Leitbuendelhuelle +verholzt. + + +Zusammenfassung der Stammanatomie + + +Umriss rund oder oval. +Leitbuendel +in einer Reihe. Epidermiszellen verholzt. Chlorenchyma in tangential +verlaengerten +Gruppen. + + +Beschreibung (Englisch) + + +Culm-diameter +2-5 mm +, wall thin, radius of culm in relation to wall thickness approximately 1:0.25 or <0.25. Outline circular with a smooth surface. Culm-center hollow and surrounded by a few thin-walled, not lignified cells. Epidermis-cells thin-walled all around. Large vascular bundles arranged in one peripheral row. Chlorenchyma in tangentially enlarged groups. Sclerenchyma in a large, peripheral continuous belt (> 3 cells). Cells thick-walled. Small sclerenchymatic sheath with 1-2 cells around vascular bundles. Largest vessels in vascular bundles in lateral position. Largest vessel in the bundle 20-50 +μm +. Distinct cavities (intercellulars) in the protoxylem area of vascular bundles. + + + +Oekologie + + +Lebensform Therophyt + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + + + + + + + + + + + +
+ +6.3.9 - Robinienwald ( +Robinion +) + +
7.1 - Trittrasen und Ruderalfluren
+ +7.1.4 - +Einjaehrige +Ruderalflur ( + +Sisymbrion + +) + +
+
+ + +fett + +Dominante Art, welche das Aussehen des Lebensraumes +mitpraegt + +Charakterart +Weniger strikt an den Lebensraum gebundene Art + + +
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +maessig +trocken +Lichtzahl LhalbschattigSalzzeichen--
Reaktionszahl Rschwach sauer bis neutral (pH 4.5-7.5)Temperaturzahl T +kollin ( +Laubmischwaelder +mit Eichen) +
+Naehrstoffzahl +N + +naehrstoffreich + +Kontinentalitaetszahl +K +subkontinental (niedrige relative Luftfeuchtigkeit, grosse Temperaturschwankungen, eher kalte Winter)
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Bromus sterilis +L. + + + + + + +Volksname Deutscher Name: +Taube Trespe +Nom +francais +: + +Brome +sterile + +Nome italiano: +Forasacco rosso + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Bromus sterilis L. + + +Checklist 2017 + +67200
= +Bromus sterilis L. + + +Flora Helvetica 2001 + +2602
= +Bromus sterilis L. + + +Flora Helvetica 2012 + +2778
= +Bromus sterilis L. + + +Flora Helvetica 2018 + +2778
= +Bromus sterilis L. + + +Index synonymique 1996 + +67200
= +Bromus sterilis L. + + +Landolt 1977 + +366
= +Bromus sterilis L. + + +Landolt 1991 + +330
= +Bromus sterilis L. + + +SISF/ISFS 2 + +67200
= +Bromus sterilis L. + + +Welten & Sutter 1982 + +2248
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Status Indigenat +: Archeophyt: vor der Entdeckung von Amerika in der Region aufgetreten (vor 1500) + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein + + +Status Rote Liste national 2016 + + +Status IUCN +: Nicht +gefaehrdet + + + +Zusaetzliche +Informationen + +Kriterien IUCN: -- + + +Status Rote Liste regional 2019 + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Biogeografische RegionenStatusKriterien IUCN
Jura (JU) +nicht +gefaehrdet +(Least Concern) +
Mittelland (MP) +nicht +gefaehrdet +(Least Concern) +
Alpennordflanke (NA) +nicht +gefaehrdet +(Least Concern) +
+Alpensuedflanke +(SA) + +nicht +gefaehrdet +(Least Concern) +
+Oestliche +Zentralalpen (EA) + +nicht +gefaehrdet +(Least Concern) +
Westliche Zentralalpen (WA) +nicht +gefaehrdet +(Least Concern) +
+
+ + +Status nationale +Prioritaet +/Verantwortung + + + + + + + +
+Keine nationale +Prioritaet +oder internationale Verantwortung +
+
+ +Schutzstatus + + + + + + +
Kein internationaler, nationaler oder kantonaler Schutz
+
+
+
+
\ No newline at end of file diff --git a/data/38/DB/2C/38DB2C3268845B26A9D7F73380B717D6.xml b/data/38/DB/2C/38DB2C3268845B26A9D7F73380B717D6.xml new file mode 100644 index 00000000000..42bcac64340 --- /dev/null +++ b/data/38/DB/2C/38DB2C3268845B26A9D7F73380B717D6.xml @@ -0,0 +1,1302 @@ + + + +A new species of Illacme from southern California (Siphonophorida, Siphonorhinidae) + + + +Author + +Marek, Paul E. +https://orcid.org/0000-0002-7048-2514 +Virginia Polytechnic Institute and State University, Department of Entomology, Blacksburg, Virginia 24061, USA +paulemarek@gmail.com + + + +Author + +Hall, Charity L. +Blacksburg, Virginia 24060, USA + + + +Author + +Lee, Cedric +University of California, Berkeley, Department of Environmental Science, Policy, and Management, California, 94720, Berkeley, USA + + + +Author + +Bailey, James +https://orcid.org/0000-0001-5861-939X +Long Beach, California, 90803, USA + + + +Author + +Berger, Matt C. +West Virginia University, Division of Plant and Soil Sciences, Morgantown, West Virginia, USA + + + +Author + +Kasson, Matt T. +West Virginia University, Division of Plant and Soil Sciences, Morgantown, West Virginia, USA + + + +Author + +Shear, William +https://orcid.org/0000-0002-5887-7003 +Hampden-Sydney College, Hampden Sydney, Virginia, USA + +text + + +ZooKeys + + +2023 + +2023-06-21 + + +1167 + + +265 +291 + + + + +http://dx.doi.org/10.3897/zookeys.1167.102537 + +journal article +http://dx.doi.org/10.3897/zookeys.1167.102537 +1313-2970-1167-265 +D97DDFD19B484432BE9246E4743C44EA +23AFA116ED7358A1B2C53AC9885EEA67 + + + + + +Illacme socal Marek & Shear +sp. nov. + + + + +Figs 1 +, 2 +, 3 +, 4 + + + + +Illacme +"Santa Ana" +Marek et al. 2021 +: 3. + + + +Type material. + +Holotype +: United States - +California +• ♂; Orange County, Lake Forest, Whiting Ranch Wilderness Park, junction of Serrano and Line Shack roads; +33.67943°N +, - +117.64629°W +, elev. 272.8 m; 21 December 2018; 13:28; P. Marek, C. Hall leg.; VTEC, MPE04621. +Paratypes +: United States - +California +• 8 ♂, 11 ♀; same collection data as for holotype; VTEC, MPE04622, MPE04963-4977; VMNH, MPE04624; UCDC, MPE04625. +Non-type material +: United States - +California +• 4 ♂, 5 ♀; Orange County, Lake Forest, Whiting Ranch Wilderness Park, junction of Serrano Road and Live Oak Trail; +33.679406°N +, - +117.647208°W +, elev. 268 m; 18 January 2022; 16:41; M. Berger leg.; VTEC, MPE05265-5274. + + + +Diagnosis. + +Adult males of + +I. socal + +sp. nov. are distinct from + +I. plenipes + +and + +I. tobini + +based on the combination of: Metazonites slightly wider than prozonites, with faintly enlarged paranota (Suppl. material 5: fig. S17), not subequal in width as in + +I. plenipes + +nor noticeably wider as in + +I. tobini + +. Ozopore peritreme with two large backwards projecting spines (sp, Suppl. material 5: fig. S20) as in + +I. plenipes + +, not lacking two large spines as in + +I. tobini + +. Ozopore ringed with ca. 14 setae. Ozopores situated inside (mediad) lateral margin, oriented dorsally (Suppl. material 5: fig. S17) as in + +I. plenipes + +, not dorsolaterally and near lateral margin as in + +I. tobini + +. Metazonite posterior margin (limbus) lined with anchor-shaped, posteriorly projecting spines as in + +I. plenipes + +( +an +, Suppl. material 5: figs S17, S20); spines not quadrate-shaped as in + +I. tobini + +. Posterior margin of metazonite straight as in + +I. plenipes + +, not sinuate with anteriorly curved paramedial margins as in + +I. tobini + +(Suppl. material 5: fig. S17). Telson densely covered with irregularly oriented and unevenly distributed stout spines on lateral surface only (Suppl. material 6: fig. S22) as in + +I. tobini + +; telson not covered with stout spines on all surfaces nor with posterior margin lined with posterodorsally oriented anchor-shaped spikes as in + +I. plenipes + +. Hypoproct with> 2 setae present arranged in a setal row as in + +I. plenipes + +(Suppl. material 6: fig. S22), not as in + +I. tobini + +with two setae. Anterior gonopodal apex (podomere 7) with four spines (+ 1 tarsungulum) (Fig. +3A +; Suppl. materials 6, 7: figs S23-S27), not three spines (+ 1 tarsungulum) as in + +I. plenipes + +nor spinose with eight spines (+ 1 tarsungulum) as in + +I. tobini + +. Anterior gonopodal podomere 3 with two long setae as in + +I. tobini + +(Fig. +3A +), not ringed with six setae as in + +I. plenipes + +. Posterior gonopodal apex (podomere 7) comprising a bundle of five styliform articles, with one article (the tarsungulum) spike-shaped +(i-v +, Fig. +3B +; Suppl. material 7: figs S25-S27), not bundle of three styliform articles as in + +I. plenipes + +nor four styliform articles as in + +I. tobini + +. The differential diagnosis of + +I. socal + +sp. nov., + +I. tobini + +and + +I. plenipes + +is summarized in Table +1 +, and a comparison of measurements between these species for a male individual with an equivalent number of rings shown in Table +2 +. + + + +Table 1. +Differential diagnostic characters of + +Illacme socal + +sp. nov., + +Illacme tobini + +and + +Illacme plenipes + +. (*) indicates revisions to Table +1 +from +Marek et al. 2016 +. (**) indicates that there is also a seta below the bundle that is not counted. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
- + +Illacme tobini + + + +Illacme plenipes + + + +Illacme socal + +sp. nov. +
+Rings + +Metazonites wider than prozonites ( +Marek et al. 2016 +: fig. 10A) + +Metazonites subequal in width ( +Marek et al. 2016 +: fig. 10B) +Metazonites slightly wider than prozonites (Suppl. material 5: fig. S17)
+Peritreme + +2 large backwards projecting spines absent ( +Marek et al. 2016 +: fig. 16E) + +2 large backwards projecting spines present ( +Marek et al. 2016 +: fig. 16F) + +2 large backwards projecting spines present ( +sp +, Suppl. material 5: fig. S20) +
+Metazonite anterior margin adornment +* +Without tubercles or adornment along anterior margin of metazonite*3 or 4 stout flat tubercles opposite ozopore near anterior margin, lunate arrangement encircling ozopore*Row of stout flat tubercles along anterior margin of metazonite; tubercles absent medially
+Metazonite posterior margin adornment + +Lined with quadrate backwards projecting spines ( +Marek et al. 2016 +: fig. 10C, E) + +Lined with anchor-shaped backwards projecting spines ( +Marek et al. 2016 +: fig. 10D, F) + +Lined with anchor-shaped backwards projecting spines ( +an +, Suppl. material 5: figs S17, S20) +
+Metazonite posterior margin shape + +Sinuate, with anteriorly curved paramedial margins ( +Marek et al. 2016 +: fig. 10A) + +Straight, without curvature ( +Marek et al. 2016 +: fig. 11B) +Straight, without curvature (Suppl. material 5: fig. S17)
+Telson + +Covered with stout spines on lateral surface only ( +Marek et al. 2016 +: fig. 11A) + +Covered with stout spines on all surfaces ( +Marek et al. 2016 +: fig. 11B) +Covered with stout spines on lateral surface only (Suppl. material 6: fig. S22)
+Hypoproct + +2 setae present ( +Marek et al. 2016 +: fig. 11A) + +> 2 setae present, in a setal row ( +Marek et al. 2016 +: fig. 11B) +> 2 setae present, in setal row (Suppl. material 6: fig. S22)
+Anterior gonopodomere 3 + +2 setae present ( +Marek et al. 2016 +: fig. 8E) + +6 setae present ( +Marek et al. 2016 +: fig. 8F) + +2 setae present (Fig. +3A +) +
+Anterior gonopodal apex + +8 spines + 1 tarsungulum ( +Marek et al. 2016 +: fig. 9C)* + +3 spines + 1 tarsungulum ( +Marek et al. 2016 +: fig. 9D)* + +4 spines + 1 tarsungulum (Fig. +3A +; Suppl. +materials +6, 7: figs S23-S27) +
+Posterior gonopodal apex +** + +Bundle of 4 styliform articles, with one these articles (the tarsungulum) spike-shaped ( +Marek et al. 2016 +: figs 11C, 12B)* + +Bundle of 3 styliform articles, with one these articles (the tarsungulum) spike-shaped ( +Marek et al. 2016 +: fig. 11D)* + +Bundle of 5 styliform articles, with one these articles (the tarsungulum) spike-shaped ( +i +- +v +, Fig. +3B +; Suppl. material 7: figs S25-S27) +
+
+ + +Table 2. +Comparison of counts (p, a, l, p + a + T) and measurements between + +Illacme socal + +sp. nov., + +Illacme tobini + +, and + +Illacme plenipes + +for a male individual with an equivalent number of rings. Measurements are reported in millimeters. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
-palHWHLISWAWCW
+ + +I. tobini + +(MPE00735) + +10624140.340.390.210.110.44
+ + +I. plenipes + +(SPC000932) + +10524020.310.400.190.100.40
+ + +I. socal + +sp. nov. (MPE04621) + +10213980.310.390.200.100.40
+ + +I. socal + +sp. nov. (MPE04622) + +11814620.320.380.210.100.40
- +W1 + +L1 + +H1 + +AS1 + +A7W + +P7W + +BL + +p + a + T +
+ + +I. tobini + +(MPE00735) + +0.520.200.310.430.040.0319.73106 + 2 + T
+ + +I. plenipes + +(SPC000932) + +0.400.160.400.430.050.0417.12105 + 2 + T
+ + +I. socal + +sp. nov. (MPE04621) + +0.500.120.400.430.040.0218.93102 + 1 + T
+ + +I. socal + +sp. nov. (MPE04622) + +0.520.180.390.38NANA22.47118 + 1 + T
+
+Nucleotide site substitutions. COI: A (36, 48, 51, 57, 67, 70, 75, 84, 85, 135, 138, 153, 156, 165, 181, 195, 198, 213, 243, 246, 280, 291, 294, 297, 312, 321, 366, 390, 447, 471, 486, 519, 522), C (18, 33, 55, 132, 134, 162, 172, 180, 201, 207, 240, 252, 259, 273, 276, 327, 333, 360, 361, 403, 414, 417, 429, 435, 464, 493, 505, 517, 523, 525), G (32, 74, 97, 100, 117, 120, 216, 264, 287, 292, 300, 433, 454, 501), T (25, 30, 54, 81, 96, 102, 105, 114, 147, 177, 222, 258, 262, 282, 303, 318, 369, 372, 378, 384, 393, 396, 409, 420, 423, 450, 459, 468, 469, 483, 504, 556, 559, 561, 570, 576). +
+ +Description of holotype. + +(♂) (Fig. +1 +). Counts and measurements: p = 102. a = 1. l = 398. (102 + 1 + T). BL = 18.93. HW = 0.31. HL = 0.39. ISW = 0.20. AW = 0.10. CW = 0.40. W1 = 0.50. L1 = 0.12. H1 = 0.40. AS1 = 0.43. A7W = 0.04. P7W = 0.03. Head pear-shaped, tapered anteriorly to round point at a 130° angle from antennal sockets; occiput gradually curved medially towards occipital foramen (Suppl. materials 1, 9: figs S1, S2, S32, S34). Head covered with long slender, erect setae (Fig. +2 +; Suppl. materials 1, 9: figs S1-S3, S32). Gnathochilarium and labrum closely appressed, tapered anteriorly to round point (Suppl. materials 1, 3, 9: figs S1, S3, S10-S12, S32). Labrum with anteromedial tooth-lined orifice ( +to +, Fig. +4 +; Suppl. materialS 3,4: figs S9, S13, S14). Labral surface without noticeable pores (Fig. +4 +). (However, the apparent lack of labral pores may be a result of specimen preparation for microscopy. Labral pores are present in + +I. plenipes + +and + +I. tobini + +. A few pores may be visible in Fig. +4A +). Shelf-like carina projecting dorsally from labrum-epistome margin ( +sh +, Fig. +4 +; Suppl. material 4: figs S13, S15). Gnathochilarium and head capsule noticeably separate, with thin gap visible between ( +gp +, Suppl. material 3: fig. S10). Gnathochilarium thin plate-like, occupying nearly entire ventral surface of head (Suppl. material 3: fig. S10). Gnathochilarium tightly appressed to ventral surface of head capsule, leaving a small gap anteriorly between labrum, gnathochilarial stipes. Gnathochilarium with sclerites: stipes ( +st +), mentum ( +me +), postmentum ( +pm +), lamellae linguales ( +ll +), cardines ( +cd +) ( +cd +, +ll +, +me +, +pm +, +st +, Suppl. material 3: fig. S10). Gnathochilarial cardo (mistakenly homologized with the mandibular cardo in +Marek et al. 2016 +) noticeable between head capsule, gnathochilarial stipes ( +cd +, Suppl. material 3: fig. S10). Stipes of gnathochilarium with inner, outer palps; outer, inner palps with 2, 3 setae, respectively ( +ip +, +op +, Fig. +4 +; Suppl. materials 3, 4: figs S10, S13). Lamellae linguales with subapical palps ( +lp +, Suppl. material 3: fig. S10). Mandibles not externally visible (Fig. +4 +; Suppl. materials 1, 3: figs S1, S10). Mandible spear shaped, ca. 1/2 length of gnathochilarium (Fig. +4 +; Suppl. materials 3, 4: figs S11, S15). Mandible with pectinate lamella and four or five flabellate external teeth ( +md +, +et +, +pl +, Suppl. material 4: figs S13-S16). Molar plate absent. Mandibular pectinate lamella with numerous rows of jagged ventrally projecting serrulae, nested in groove of endochilarial frontal body (Fig. +4 +; Suppl. material 4: figs S13-S16). Endochilarium with V-shaped frontal body. Endochilarium with fringed lobes ( +'spatulae' +sensu Silvestri, 1903) that protrude distally through gnathochilarial stipes and lamellae linguales ( +fl +, Fig. +4 +; Suppl. material 4: figs S13, S14). Antennae sub-geniculate, elbowed between antennomeres 3 and 4 (Figs +1 +, +2 +; Suppl. materials 1, 10, 11: figs S1-S4; S36, S42). Antennae comprising eight antennomeres, 5 and 6 enlarged. Five sensillum types: four apical cones (AS) oriented in a trapezoidal cluster on eighth antennomere, with longitudinally grooved outer surface and circular pores apically ( +as +, Fig. +2 +; Suppl. material 2: figs S6-S8). Chaetiform sensilla (CS) widely spaced on antennomeres 1-7, each sensillum with one or two barbules ( +cs +, Fig. +2 +; Suppl. materials 1, 2: figs S1-S8). Trichoid sensilla (TS) oriented apically encircling antennomeres 6, 7, lacking barbules ( +ts +, Fig. +2 +; Suppl. material 2: figs S5, S6). Small basiconic sensilla (Bs2) in rows of six and seven oriented apical dorsally (retrolaterally) on antennomeres 5 and 6; smooth, capsule-shaped, 1/2 length of chaetiform sensillum ( +b2 +, Fig. +2 +; Suppl. material 2: figs S5, S6). Spiniform basiconic sensilla (Bs3) in row of 4, oriented apical dorsally on antennomere 7 (on longitudinal axis with Bs2 on antennomeres 5, 6); sensilla tips facing apical cones; each sensillum with ca. 3 barbules encircling tip ( +b3 +, Fig. +2 +; Suppl. material 2: figs S6, S7). Two auxiliary spiniform basiconic sensilla, each on distal rim of antennomere 7 oriented 120° from row of four (Suppl. material 2: fig. S6). Antennae extend posteriorly to middle of tergite 3. Relative antennomere lengths 6>2>5>3>4>1>7>8. Collum not concealing head, with straight anteromedial edge, gradually tapering laterally (Suppl. materials 1, 11: figs S1, S40-S42). Lateral margin of collum rounded, with thickened scaly carina (Suppl. materials 1, 3: figs S4, S10). This carina repeated serially on lateral tergal and pleural margins (absent from telson). Lateral tergal and pleural carinae jagged, saw-like (potentially interlocking), pronounced on midbody rings (Fig. +1 +, Suppl. material 5: fig. S18). Metazonites slightly wider than prozonites, with faintly enlarged paranota (Suppl. materials 5, 11: figs S17, S39, S40). Metazonites slightly arched (Suppl. material 9: fig. S32). Metazonite dorsally covered with long, slender setae (Fig. +1 +; Suppl. material 11: figs S40, S41). Tergal setae hollow; tipped with translucent silk-like exudate, exudate sometimes tangled with neighboring setae ( +ex +, Suppl. material 9: fig. S35). Metazonite posterior margin (limbus) lined with anchor-shaped posteriorly projecting spines ( +an +, Suppl. material 5: figs S17, S20). With row of conical spines anterior to limbus on ozoporiferous rings only (Suppl. material 5: figs S17, S20). Limbal anchor-shaped spikes alternating in size (large, small-sometimes large, small, small, large) along margin. Ozopores oriented dorsally, located near limbus (Suppl. material 5: fig. S17). Ozopores absent from collum, tergites 2-4, telson. Ozopores elevated faintly on peritremata (porosteles absent), with two large backwards projecting spines, encircled with ca. 14 robust setae ( +sp +, Suppl. material 5: fig. S20). Row of stout flat tubercles along anterior margin of metazonite; tubercles absent medially. Posterior half of body with rings more convex (Suppl. material 10: fig. S37), posterior-most tergites covered with a greater density of long, slender setae (Suppl. material 5: fig. S18). Apodous ring without visible sternum, pleurites contiguous in midline. Apodous tergite densely setose, with unevenly distributed spikes localized to posterolateral corner; posterior margin lined with posteriorly oriented anchor-shaped spikes (Fig. +3A +; Suppl. material 6: fig. S22). Telson covered with dorsally oriented stout spines on lateral surface only; without anchor-shaped spikes on margin (Suppl. material 6: fig. S22). Prozonite highly sculptured, with 2-4 rows of discoidal flat tubercles (Suppl. material 5: fig. S20). Tubercles in two shape classes: posterior prozonal tubercles button-shaped protuberant ( +tb +); anterior tubercles flush ( +tf +) with surface anteriorly ( +tb +, +tf +, Suppl. material 5: fig. S20). Pleurites quadrate, flat, with jagged scaly lateral, posterior, medial margins (Fig. +1 +). Pleurite medial margin broad, with scaly raised carina (Fig. +1 +). Pleurites plate-like, large, composing 4/5 of ventral ring area. Pleural medial margins overlapping lateral sternal margins, covering spiracles (Fig. +1 +). Sternites heart-shaped, wider anteriorly. Anterior, posterior sternites free, separate from pleurites (Suppl. material 5: fig. S19). Sternum with prominent midline triangular ridge projecting ventrally, tapering to a point anteriorly ( +rd +, Suppl. material 5: fig. S19). Sternum with spiracles and legs oriented posteroventrally (Fig. +1 +; Suppl. material 5: fig. S19). Spiracles circular, orifice open, hollow; oriented (above) dorsal to legs (Suppl. material 5: fig. S19). Tergites, pleurites, sternites separated by arthrodial membrane (Suppl. materials 5, 6: figs S18, S19, S22). Arthrodial membrane between tergites, pleurites wider posteriorly, pleated, thereby allowing telescoping body rings. Telson, paraprocts covered with long slender erect setae (Suppl. materials 5, 6: figs S18, S19, S22). Setae on epiproct margin have inflated bases (potentially glandular in nature). Paraprocts quarter-spherical, anterior margins faintly scaly (Suppl. material 6: fig. S22). Hypoproct small, ca. 1/8 area of paraproct, with four posterior projecting setae. Legs (postgonopodal) with seven podomeres (relative lengths denoted by numbers; 1 longest, 7 shortest): coxa (6), trochanter (7), prefemur (2), femur (3), postfemur (5), tibia (4), and tarsus (1). Legs with sparse setae, appearance similar to chaetiform sensilla with one or two barbules. Coxae nearly contiguous medially, separated by narrow sternal ridge. Coxa (postgonopodal legs) with large posteroventrally oriented D-shaped opening for eversible sac (Fig. +1 +; +es +, Suppl. material 5: fig. S19). Eversible sacs membranous, distended slightly from aperture (Fig. +1 +). Tarsus with pincer-like claw, dorsal claw arcuate; ventral accessory claw thinner, arcuate, 1/2 length of dorsal claw (Suppl. materials 5, 6: figs S18, S22). Second leg pair with posteriorly oriented coxal gonapophyses; rounded, protuberant. Ninth, tenth leg pairs modified into gonopods, each comprising seven podomeres (Fig. +3 +; Suppl. materials 6, 7: figs S23-S27). Anterior gonopod, ninth leg pair, robust, thicker than posterior gonopod, tenth leg pair (Fig. +3A +; Suppl. material 7: fig. S25). Anterior gonopodal apex (podomere 7) spade-shaped; in repose cupped around flagelliform posterior gonopodal apex (podomere 7). Anterior gonopodal podomere 7 with four spines + 1 tarsungulum (Fig. +3A +; Suppl. materials 6, 7: figs S23-S27). Anterior gonopodal podomere 3 with two setae. Posterior gonopodal podomere 7 deeply divided, comprising a bundle of five styliform articles, with one these articles (the tarsungulum) spike-shaped ( +i +- +v +, Fig. +3A +; Suppl. material 7: figs S25-S27). Four dorsal-most, longest articles laminate distally, recurving laterally, with denticulate posterior margins ( +i +- +iv +, Fig. +3B +; Suppl. material 7: figs S25-S27). Ventral-most, fifth article spike-like ( +v +, Fig. +3B +). Accessory seta located proximal to fifth spike-like article at base of podomere ( +s +, Fig. +3B +). Triangle-shaped sterna present between left and right gonopods of ninth and tenth leg pairs, thicker between posterior gonopods. Supplementary micrographs of + +I. socal + +sp. nov. are archived in the Dryad Data Repository at: https://doi.org/10.5061/dryad.x95x69pq7. + + + +Figure 1. + +Illacme socal + +sp. nov. +A +♂ holotype, MPE04621, and ♀ paratype, MPE04622 (with head at top) +B +scanning electron micrograph of the head of ♀, MPE04625 +C +micrograph of midbody rings of ♀, ventral view, MPE04625. Scale bars: 1 mm ( +A +); 0.5 mm ( +B, C +). + + + + +Figure 2. + +Illacme socal + +sp. nov. Scanning electron micrographs +A +left, head and anterior rings of ♂ holotype, ventral view (MPE04621) +B +right antenna of ♀ paratype, apical view (MPE04976). Scale bars: 400 +µm +( +A +); 50 +µm +( +B +). Abbreviations: +as +, apical cones; +b2 +, small basiconic sensillum; +b3 +, spiniform basiconic sensillum; +cs +, chaetiform sensillum; +ts +, trichoid sensillum. + + + + +Figure 3. + +Illacme socal + +sp. nov. ♂ +A +anterior gonopod, left side, medial view +B +posterior gonopod, left side, medial view. Podomeres numbered. Scale bar: 50 +µm +( +A, B +). Abbreviations: +i +- +v +, styliform articles of the posterior gonopodal apex (podomere 7); +s +, accessory seta. + + + + +Figure 4. + +Illacme socal + +sp. nov. Scanning electron micrographs +A +labrum of ♀ paratype, dorsal view (MPE04625) +B +mandible of ♂ paratype, lateral view (medially sectioned with left side of head removed), gnathochilarium at top (MPE04971) +C +posterior-most rings and telson of ♂ holotype, ventral view (MPE04621). Scale bars: 50 +µm +( +A, B +); 250 +µm +( +C +). Abbreviations: +ip +, inner palps; +ll +, lamellae linguales; +md +, mandible; +me +, mentum; +sh +, shelf-like carina projecting dorsally from labrum-epistome margin; +st +, stipes; +to +, anteromedial tooth-lined orifice on labrum. + + + + +Description of largest paratype. + +(♀) VTEC (MPE04622) - Counts and measurements: p = 118. a = 1. l = 462. (118 + 1 + T). HW = 0.32. HL = 0.38. ISW = 0.21. AW = 0.10. CW = 0.40. W1 = 0.52. L1 = 0.18. H1 = 0.39. AS1 = 0.38. BL = 22.47. Morphology similar to male holotype. In combination with its counts and measurements, the following structures of female paratype differ from male holotype. Head chevron-shaped, tapered anteriorly to round point at a 120° angle anterior from antennal sockets (Fig. +1 +; Suppl. material 11: figs S36, S39); occipital area posterior from antennal sockets nearly straight, faintly curved medially towards occipital foramen (Suppl. material 11: fig. S41). Cyphopods large, area 1/6 the ring area in its widest cross-section; almond-shaped, bivalvular, narrow apex oriented ventrally. + + + +Variation. + +There is negligible variation in coloration between live specimens. Female specimens are generally larger in size (greater head, ring width) and have more rings and legs. The predominant source of variation between specimens is ring and leg counts (Tables +2 +, +3 +). Females have a maximum of 125 rings (486 legs maximum) with a median of 94, and males a maximum of 104 rings (402 legs maximum) with a median of 73. The rings of + +I. socal + +sp. nov. (males and females) are uniform in length, width, and height along the trunk, but are slightly taller and more convex in posterior rings. + + + +Table 3. + +Illacme socal + +sp. nov. ring (p + a) and leg counts. Sorted by sex, ring count (descending). + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
SpecimenSexRing countLeg count
MPE05266F125486
MPE04622F119462
MPE05265F116450
MPE04625F115446
MPE04624F103398
MPE04966F102394
MPE04623F98378
MPE04963F96370
MPE05268F92354
MPE05267F90346
MPE04965F85326
MPE05270F84322
MPE04974F67254
MPE04976F57214
MPE04973F47174
MPE04964F44162
MPE04977M104402
MPE04621M103398
MPE04970M96370
MPE05274M83318
MPE05271M75286
MPE05272M75286
MPE04969M71270
MPE05269M70266
MPE04967M60226
MPE04968M53198
MPE04972M52194
MPE04975M51190
+
+
+ +Ecology. + + +Illacme socal + +sp. nov. individuals were encountered during the day in a California live oak woodland habitat surrounded by chaparral shrubland (Fig. +5 +). One female individual was found beneath a dead oak log, and the others were encountered beneath the humus layer and embedded within the underlying soil matrix (Suppl. material 8: figs S28-S31). Co-occurring dominant flora included California live-oak ( + +Quercus agrifolia + +), California sagebrush ( + +Artemisia californica + +), California broom ( + +Acmispon glaber + +), hollyleaf redberry ( + +Rhamnus ilicifolia + +), Pacific poison-oak ( + +Toxicodendron diversilobum + +), and Coastal cholla ( + +Cylindropuntia prolifera + +). Other invertebrates encountered included centipedes ( + +Arenophilus iugans + +Chamberlin, 1944, + +Taiyuna isantus + +(Chamberlin, 1909), + +Oabius + +Chamberlin, 1916), beetles ( + +Eleodes osculans + +, + +Apsena + +sp.), and arachnids ( + +Hubbardia + +sp., + +Cicurina + +sp.). Between the collection of the type material by PEM in 2018 and nontype material by MCB in 2022, the Silverado fire (26 October-7 November 2020) burned ca. 12,500 acres including portions of Whiting Ranch Wilderness Park. The impact of this fire on the + +I. socal + +sp. nov. population remains unclear, but given their efficient burrowing locomotion (see behavior below), this species likely minimizes fire risk by staying in deeper soils with higher soil moisture. + + + +Figure 5. +Habitat of + +Illacme socal + +sp. nov. Whiting Ranch Wilderness Park, Orange County, California +A +California live oak woodland habitat surrounded by chaparral shrubland +B +close up of oak woodland habitat +C +type locality beneath oak canopy +D +an + +I. socal + +sp. nov. individual (center) encountered beneath the humus layer and embedded within the underlying soil matrix. + + + + +Behavior. + +When uncovered, individuals were observed spiraling downward into the soil cavity via a corkscrew-like pattern. Filmed in the laboratory, and within the soil from its microhabitat, the burrowing locomotion of a female + +I. socal + +sp. nov. was slow (100 +µm +/s), undulatory, and continuous (MPE04624, Suppl. material 12: https://vimeo.com/823446011?share=copy). The sinuous locomotory movement of the millipede appeared to follow a path of low resistance and track the topography within the soil matrix. While burrowing, a single orientation was not continually maintained, and the individual repeatedly turned and continued motion several times in different planes. While passing through a narrow junction, + +I. socal + +sp. nov. appeared to squeeze through the crevice by reduction of its body height by ca. 1/2 (Suppl. material 12: https://vimeo.com/823446011?share=copy, at 34 s). After squeezing into the interstice, and through cephalic nodding and dorso-ventral arching of the trunk, the millipede forcibly enlarged the interstice. The body rings did not appear to telescope into one another while passing through narrow junctions. Moving within the soil matrix, the millipede appeared to be positively thigmotactic to contact with the soil. The millipede appeared to navigate by aid of its large antennae, and detection of interstitial voids seemed to be mediated by these appendages. The antennae moved rapidly, and the left and right antennae, each equally and continually, tapped on the soil grains. As it walked, the millipede was observed asymmetrically extending one antenna into the soil lacunae ahead as if the sole appendage was used as a probe by the blind millipede to survey ahead of itself in the confined subterranean space (Suppl. material 12: https://vimeo.com/823446011?share=copy, at 30 s). + + + +Distribution. + +Only known from its type locality at Whiting Ranch Wilderness Park. An observation by CL from Los Angeles County at Eaton Canyon Natural Area in Pasadena, California, appears consistent with + +I. socal + +sp. nov. in morphological features. This millipede, a juvenile and of uncertain species identity due to lack of species-diagnostic gonopods, was observed on 10 February 2021; iNaturalist, observation: 69384055. + + + +Etymology. +The species name refers to its type locality in Southern California, commonly shortened to SoCal. + +
+
+
\ No newline at end of file diff --git a/data/38/DB/EF/38DBEF99CBAB821D4E9864BA0618EE46.xml b/data/38/DB/EF/38DBEF99CBAB821D4E9864BA0618EE46.xml new file mode 100644 index 00000000000..b6b58616ac9 --- /dev/null +++ b/data/38/DB/EF/38DBEF99CBAB821D4E9864BA0618EE46.xml @@ -0,0 +1,77 @@ + + + +Order Scandentia + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +104 +109 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Tupaia moellendorffi +subsp. +moellendorffi +Matschie 1898 + + + + + + + +Tupaia moellendorffi +subsp. +moellendorffi +Matschie 1898 + +, +Sitzb. Ges. Naturf. Fr. Berlin: 39 + +. + + + + +Type Locality: + +Philippines +, Culion Isl. + + + + + \ No newline at end of file diff --git a/data/38/DC/14/38DC149B58EB121D04E912184FEF832F.xml b/data/38/DC/14/38DC149B58EB121D04E912184FEF832F.xml new file mode 100644 index 00000000000..5dc837bb345 --- /dev/null +++ b/data/38/DC/14/38DC149B58EB121D04E912184FEF832F.xml @@ -0,0 +1,80 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part R) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +785 +805 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Robinia spinosa +Linnaeus + +, + +Mantissa Plantarum Altera + +: 269. 1771 + + +. + + + +"Habitat in Sibiriae montibus arenosis siccissimis Salengiae et Kiaechae." RCN: 5454. + + +Type not designated. + + +Original material: none traced. + + + +Current name: + +Caragana spinosa +(L.) Hornem. + +( +Fabaceae +: +Faboideae +). + + + + \ No newline at end of file diff --git a/data/38/DC/CF/38DCCF23446741C3F161851DAA4314E9.xml b/data/38/DC/CF/38DCCF23446741C3F161851DAA4314E9.xml new file mode 100644 index 00000000000..e6f0f231c52 --- /dev/null +++ b/data/38/DC/CF/38DCCF23446741C3F161851DAA4314E9.xml @@ -0,0 +1,83 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part V) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +911 +926 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Vitis vinifera +Linnaeus var. +apyrena +Linnaeus + +, + +Species Plantarum +1 + +: 202. 1753 + + +. + + + +RCN: 1639. + + +Type not designated. + + +Original material: none traced. + + + +Current name: + + +Vitis vinifera + +L. + +( +Vitaceae +). + + + + \ No newline at end of file diff --git a/data/38/DD/16/38DD167111FEAB5C92FE78C2471B1D9A.xml b/data/38/DD/16/38DD167111FEAB5C92FE78C2471B1D9A.xml new file mode 100644 index 00000000000..94a01b12135 --- /dev/null +++ b/data/38/DD/16/38DD167111FEAB5C92FE78C2471B1D9A.xml @@ -0,0 +1,473 @@ + + + +Info Flora Schweiz - Rosaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/rosaceae.html + +url + + + + + +Potentilla collina +Wibel + + + + + + +Huegel-Fingerkraut + + + + + +Art ISFS: 321900 Checklist: 1035780 +Rosaceae +Potentilla +Potentilla collina +aggr. +Potentilla collina Wibel + + +Zusammenfassung + + + + +Artbeschreibung + +(nach +Lauber & al. 2018 +) + +: +20-30 cm +hoch, bogig aufsteigend, weissfilzig und +spaerlich +langhaarig. +Blaetter +5 +zaehlig +, etwas lederig, die +grundstaendigen +zur +Bluetezeit +meist vertrocknet, +Teilblaetter +jederseits mit 2-4 stumpfen +Zaehnen +. +Blueten +lebhaft gelb. + + + + +Bluetezeit + +(nach +Lauber & al. 2018 +) + +: 5-7 + + +Standort und Verbreitung in der Schweiz + +(nach +Lauber & al. 2018 +) + +: +Trockenplaetze +/ kollin / Nordschweiz, Verbreitung +ungenuegend +bekannt + + +Oekologische +Zeigerwerte + +(nach +Landolt & al. 2010 +) + +1 + w32-44 + 5.h.2n=35,42,84 + + + +Status + + + +Status IUCN +: +Ungenuegende +Datengrundlage + + + + + +Oekologie + + + +Lebensform +Mehrjaehriger +Hemikryptophyt + + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + +KEINE ANGABE + + +
+
+
+
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +trocken; Feuchtigkeit +maessig +wechselnd ( ++/- +1-2 Stufen) +Lichtzahl LhellSalzzeichen--
Reaktionszahl Rschwach sauer bis neutral (pH 4.5-7.5)Temperaturzahl Twarm-kollin
+Naehrstoffzahl +N + +naehrstoffarm + +Kontinentalitaetszahl +K +kontinental (sehr niedrige Luftfeuchtigkeit, sehr grosse Temperaturschwankungen, kalte Winter)
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Potentilla collina +Wibel + + + + + + +Volksname Deutscher Name: + +Huegel-Fingerkraut + +Nom +francais +: +Potentille des collines +Nome italiano: +Cinquefoglie collinare + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Potentilla collina Wibel + + +Checklist 2017 + +321900
= +Potentilla collina Wibel + + +Flora Helvetica 2001 + +962
= +Potentilla collina Wibel + + +Flora Helvetica 2012 + +438
= +Potentilla collina Wibel + + +Flora Helvetica 2018 + +438
= +Potentilla collina Wibel + + +Index synonymique 1996 + +321900
= +Potentilla collina Wibel + + +SISF/ISFS 2 + +321900
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Status Indigenat +: Indigen + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein + + +Status Rote Liste national 2016 + + +Status IUCN +: +Ungenuegende +Datengrundlage + + + +Zusaetzliche +Informationen + +Kriterien IUCN: -- + + +Status Rote Liste regional 2019 + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Biogeografische RegionenStatusKriterien IUCN
Jura (JU) +ungenuegende +Datengrundlage (Data Deficient) +
Mittelland (MP) +ungenuegende +Datengrundlage (Data Deficient) +
Alpennordflanke (NA)--
+Alpensuedflanke +(SA) +--
+Oestliche +Zentralalpen (EA) +--
Westliche Zentralalpen (WA)--
+
+ + +Status nationale +Prioritaet +/Verantwortung + + + + + + + +
+Keine nationale +Prioritaet +oder internationale Verantwortung +
+
+ +Schutzstatus + + + + + + +
Kein internationaler, nationaler oder kantonaler Schutz
+
+
+ + +Erhalten/ +Foerdern +Mehr Informationen Merkblatt Artenschutz Merkblatt Artenschutz + + +
+
\ No newline at end of file diff --git a/data/38/DD/19/38DD19B224BE54DE9497423A1401589A.xml b/data/38/DD/19/38DD19B224BE54DE9497423A1401589A.xml new file mode 100644 index 00000000000..98d94a15d33 --- /dev/null +++ b/data/38/DD/19/38DD19B224BE54DE9497423A1401589A.xml @@ -0,0 +1,80 @@ + + + +Four new species of isopods (Crustacea, Isopoda) from South Korea + + + +Author + +Kim, Sung Hoon +https://orcid.org/0000-0001-7271-7308 +Research Center for Endangered Species, National Institute of Ecology, Yeongyang, 36531, South Korea + + + +Author + +Yoon, Seong Myeong +Department of Biology, College of Natural Sciences, Chosun University, Gwangju 61452, South Korea & Educational Research Group for Age-associated Disorder Control Technology, Graduate School, Chosun University, Gwangju 61452, South Korea +smyun@chosun.ac.kr + +text + + +ZooKeys + + +2021 + +2021-01-13 + + +1010 + + +133 +164 + + + + +http://dx.doi.org/10.3897/zookeys.1010.59101 + +journal article +http://dx.doi.org/10.3897/zookeys.1010.59101 +1313-2970-1010-133 +4F7BF6D6061C45AE9092C633B6EE9E47 +6F0242A3DDAF5EE9BA713C847078CA73 + + + + +Genus +Neastacilla Tattersall, 1921 + + + +Type species. + + +Astacilla falclandica + +Ohlin, 1901, by subsequent designation. + + + +Diagnosis + + +(modified after +King 2003b +). + +Body cylindrical; pereonite I fused to cephalon, occasionally indicated by groove dorsally or slit ventrally; pereonite IV ~ 3-10 +x +longer than other pereonites; pereonites IV and V strongly geniculated. Antenna with one row of spines on each flagellar article. Pereopod I lacking an unguis; pereopods II-IV with claw-like dactylus, not flexible between carpus and propodus; pereopods V-VII with two claws on distal end of dactylus. + + + + \ No newline at end of file diff --git a/data/38/DD/84/38DD846D8775854B0FBE44D82856C7A3.xml b/data/38/DD/84/38DD846D8775854B0FBE44D82856C7A3.xml new file mode 100644 index 00000000000..099bc0b1f2c --- /dev/null +++ b/data/38/DD/84/38DD846D8775854B0FBE44D82856C7A3.xml @@ -0,0 +1,72 @@ + + + +Species plantarum: exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas + + + +Author + +Linnaeus, Carolus + +text + +1753 +Laurentius Salvius + +Stockholm + + + +https://doi.org/10.5962/bhl.title.669 + +book +10.5281/zenodo.3931989 +3931989 + + + + +Anemone vernalis +, +spec. nov. + + + +4. Anemone pedunculo involucrato; foliis pinnatis, flore erecto. + +Pulsatilla foliis simpliciter pinnatis: foliolis lobatis, flore erecto. +Fl. suec. 448. + + +Pulsatilla involucro piloso nitido. +Fl. lapp. 223. + + +Pulsatilla, apii folio, vernalis, flore majore. +Bauh. pin. 177. prodr. 94. +Helw. puls. 63. t.9. + + +β. Pulsatilla, apii folio, vernalis, flore minore. +Bauh. pin. 177. prodr. 94. +Helw. puls. 64. t.10. + + +γ +. Pulsatilla lutea, apii hortensis folio. +Bauh. pin. 177. +Hall. helv. - - t.6 + + + + +Habitat in +Sueciae +, +Helvetiae +sylvis sterilissimis. ♃ + + + + \ No newline at end of file diff --git a/data/38/DD/CA/38DDCA807CEB56E291BC8BF5B272570D.xml b/data/38/DD/CA/38DDCA807CEB56E291BC8BF5B272570D.xml new file mode 100644 index 00000000000..01e42d01e1c --- /dev/null +++ b/data/38/DD/CA/38DDCA807CEB56E291BC8BF5B272570D.xml @@ -0,0 +1,409 @@ + + + +Description of a new Tegenaria Latreille, 1804 from southern Turkey with remarks on the Tegenaria ariadnae species-complex (Arachnida, Araneae) + + + +Author + +Dimitrov, Dragomir +National Museum of Natural History, Bulgarian Academy of Sciences, 1 Tsar Osvoboditel Blvd, 1000 Sofia, Bulgaria +https://orcid.org/0000-0001-8999-5793 +dimitrov@nmnhs.com + +text + + +ZooKeys + + +2020 + +935 + + +47 +55 + + + + +http://dx.doi.org/10.3897/zookeys.935.52089 + +journal article +http://dx.doi.org/10.3897/zookeys.935.52089 +1313-2970-935-47 +36B3E809A5AB40139B8F95991EEB429B +4D06A6A20AD9595D8427B1DC64E908B0 + + + + +Tegenaria lazarovi +sp. nov. +Figs 1-4 +, 5-6 + + + +Type material. + +♂ holotype, 2 ♀ paratypes, Turkey, Silifke distr., Karatepe village, unnamed cave on the left side of the road Anamur-Silifke, +Akcali +Daglari +Mts. 36; +36°10'55"N +, +33°26'41"E +, altitude 182 m, wet sand; 16.07.2006; P. Stoev and S. Lazarov leg. (NMNHS); 1 ♀ paratype, the same data as holotype (SMF). + + + +Other material. +3 ♀ juveniles, the same data as holotype (NMNHS). + + +Comparative material examined. + + +Tegenaria vallei + +Brignoli, 1972. ♂ holotype, Libya, Cyrenaica, Lete Cave, Benghasi, 06.04.1966, Valle and Bianchi leg., 1 ♂ paratype, the same locality as holotype, 31.12.1967, Valle leg. (MBCG); 1 ♀ paratype, the same locality as holotype, 31.12.1967, Valle leg. (MCSN); + +Tegenaria pieperi + +Brignoli, 1979. ♀ holotype, Crete, Sitia, Agios Georgios, Megalo Katafigi Cave, 21.05.1977, H. Pieper leg. (MCSN). + + + +Etymology. +The species is dedicated to my colleague, Bulgarian arachnologist Stoyan Lazarov who provided me with the type material. He was chosen over Pavel Stoev by tossing a coin. + + +Diagnosis. + +The new species fits well in the genus + +Tegenaria + +as defined by Bolzern, Burckhardt and +Haenggi +(2013) according to its straight trochanters, the absence of dorsal spines on the patellae and the shape of the conductor. It appears closest to + +Tegenaria ariadnae + +Brignoli, 1984. The males can be separated by the following characters:(1) The DBTA of + +Tegenaria lazarovi + +sp. nov. is claw-shaped, with a sharp tip (Figs +2 +, +3 +, +9 +, +10 +), while in + +T. ariadnae + +it is more massive and with a blunt tip (Bolzern, Burckhardt and +Haenggi +2013: 769, fig 14R); (2) A lighter, less sclerotized LBTA (Figs +1 +, +2 +, +8 +, +9 +), more sclerotized in + +T. ariadnae + +(Bolzern, Burckhardt and +Haenggi +2013: 769, fig 14R, 16M); (3) A pointed, triangular VPC (Figs +1 +, +8 +), trapezoid in + +T. ariadnae + +(Bolzern, Burckhardt and +Haenggi +2013:769, fig 14Q); the females of the two species can be separated by (4) the trapezoid epigynal median plate (MPE) with a broader distal part in + +Tegenaria lazarovi + +sp. nov. (Figs +5 +, +11 +), which in + +T. ariadnae + +is broader in the basal part (Bolzern, Burckhardt and +Haenggi +2013:769, fig 14S); (5) The copulatory openings are perpendicular to the MPE and positioned to its distal part (Figs +5 +, +11 +) while in + +T. ariadnae + +they are horizontal, positioned much higher (Bolzern, Burckhardt and +Haenggi +2013: 769, fig 14S); (6) The receptacles are larger, kidney-shaped (Figs +6 +, +12 +) while being smaller and more oval in + +T. ariadnae + +(Bolzern, Burckhardt and +Haenggi +2013: 769, fig 14T, 16D). + + + +Figures 1-4. + +Tegenaria lazarovi + +sp. nov. male holotype. Palp ventral ( +1 +), palp retrolateral ( +2 +), palp dorsal ( +3 +), habitus ( +4 +). + + + + +Figures 5-7. + +Tegenaria lazarovi + +sp. nov. female paratype. Epigyne ventral ( +5 +), vulva dorsal ( +6 +), habitus ( +7 +). + + + + +Description. + +Male. +Measurements. Total length (including spinnerets) 7.66; carapace length 3.23, width 2.50; chelicerae length 1.43; clypaeus height 0.22; eye diameters AME 0.075, ALE 0.090, PME 0.090, PLE 0.090; AE separated from each other by 0.020, ALE almost touching PLE, PME separated from each other by 0.14 and from PLE by 0.080; abdomen length 4.43 (including spinnerets), width 2.05; Leg measurements I 20.71 (1.65, 5.55, 1.13, 4.80, 4.80, 2.40), II 16.96 (1.50, 4.13, 1.25, 3.75, 4.15, 2.18), III 15.79 (1.45, 3.75, 1.13, 3.45, 3.90, 2.10); IV 22.55 (1.58, 4.88, 1.13, 4.60, 5.40, 2.48). Leg spination typical for the genus. Coloration (Fig. +4 +). Carapace light brown to yellow, darker in the anterior half, gradually lightening posteriorly. Chelicerae light brown. Legs I, II light brown, legs III, IV yellow. Sternum without pattern, yellow in the center, gradually darkening to light brown at the edges. Palpal femur light brown, other segments gradually lightening, yellowish. Abdomen white, without pattern. Other somatic characters. Chelicerae with 2-3 promarginal and 5 retromarginal teeth. All trochanters straight. Colulus is a single trapezoid plate, slightly notched in the middle of the distal part. Palp (Figs +1-3 +, +8-10 +). Femur length 1.80; patella length 0.60; tibia length 2.03; cymbium length 2.93. Tibia with short retrolateral apophysis with dorsal and lateral branches. Dorsal branch (DBTA) claw-shaped with sharp end. Lateral one (LBTA) rounded, less chitinized, whitish, surrounded by a light brown more sclerotized strip (Figs +2 +, +3 +, +9 +, +10 +). Cymbium long and narrow with a slight depression dorsally (Figs +2 +, +9 +). Embolus comparatively long and thin, originating at 9 +o'clock +and ending at 2 +o'clock +position. Conductor short and broad, distal portion rounded, both dorsal and ventral part of terminal end sharp. MA membranous, long and narrow, ending in a more chitinized plate, situated between the dorsal and ventral part of the +conductor's +terminal end (Figs +1 +, +8 +). + + + +Figures 8-12. + +Tegenaria lazarovi + +sp. nov. Male holotype ( +8-10 +). Palp ventral ( +8 +), palp retrolateral ( +9 +), palp dorsal ( +10 +). Female paratype ( +11, 12 +). Epigyne ventral ( +11 +), vulva dorsal ( +12 +) Scale bars: 1.0 mm. + + + +Female. +Measurements. Total length (including spinnerets) 8.30; carapace length 3.80, width 2.50; chelicerae length 0.88; clypaeus height 0.29; eye diameters and arrangement as in male; abdomen length 4.50 (including spinnerets) width 2.25; Leg measurements I 19.14 (1.58, 4.50, 1.13, 5.63, 4.50, 1.80), II 16.71 (1.58, 4.05, 1.13, 3.90, 3.90, 2.15), III 15.41 (1.50, 3.60, 1.13, 3.38, 3.90, 1.90); IV 22.81 (1.73, 4.80, 1.13, 4.65, 5.25, 2.25). Leg spination typical for the genus. Female palpal tibia with 2 dorsal and 2 prolateral spines. Coloration (Fig. +7 +). Carapace, chelicerae and sternum as in male. All legs yellow. Palpal femur, patella and tibia yellow, tarsus light brown. Abdomen whitish to light gray, darker than in male, without pattern. Median plate of epigyne light brown, framed laterally by dark brown spots. Other somatic characters. Chelicerae with 3 promarginal and 5 retromarginal teeth. All trochanters straight. Colulus is a single trapezoid plate, slightly notched in the middle of the distal part. Epigyne and vulva (Figs +5 +, +6 +, +11 +, +12 +). Width 0.98. Epigynal median plate trapezoid, with M-shaped base, broader in the distal part. Copulatory openings vertical, situated on both sides of the median plate (Figs +5 +, +11 +). Posterior sclerite absent. Receptacles large and oval (Figs +6 +, +12 +). + + + +Figures 13-18. + +Tegenaria vallei + +Brignoli, 1972 ( +13-17 +) Male holotype ( +13-15 +) palp ventral ( +13 +) palp retrolateral ( +14 +) palp dorsal ( +15 +) Female paratype ( +16, 17 +) epigyne ventral ( +16 +) vulva dorsal ( +17 +) + +Tegenaria pieperi + +Brignoli, 1979 female holotype, epigyne ventral ( +18 +). + + + + +Distribution. +Known only from the type locality in southern Turkey. + + +Remarks. + +Two + +Tegenaria + +species known from Crete, namely + +Tegenaria pieperi + +Brignoli, 1979 and + +Tegenaria schmalfussi + +Brignoli,1976 are also similar to + +T. ariadnae + +and + +T. lazarovi + +sp. nov. + +Tegenaria pieperi + +Brignoli, 1979 is known only by the female which differs from + +T. lazarovi + +sp. nov. by the rectangular MPE and the smaller and much higher positioned receptacles (Fig. +18 +). The male of + +T. schmalfussi + +differs from + +T. lazarovi + +sp. nov. by the lack of VPC and the smaller DBTA and LBTA ( +Bosmans et al. 2013 +, figs 50-52); the female can be distinguished by the smaller MPE and different shape of the receptacles ( +Bosmans et al. 2013 +, figs 53-54). I would include in this species complex also + +Tegenaria vallei + +Brignoli, 1972, known from a cave near Benghazi, Libya. Its male can be distinguished by having conductor with entirely missing VPC (Fig. +13 +) and different DBTA and LBTA (Figs +14 +, +15 +). The female differs by the oval MPE (Fig. +16 +) and the longer receptacles (Fig. +17 +). The + +T. ariadnae + +species-complex has a typical Eastern Mediterranean distribution with three species known from Crete, one from northern Libya and one from southern Turkey (Fig. +19 +). It is interesting that + +T. lazarovi + +sp. nov. appears more closely related to species inhabiting Crete and northern Libya than to any of the + +Tegenaria + +species known from the Turkish mainland. However, the current knowledge of the spider fauna of the easternmost Mediterranean (especially in north-eastern Africa) is insufficient to provide an explanation for this observation. + + + +Figure 19. +Distribution of the + +Tegenaria ariadnae + +species-complex. + + + + + \ No newline at end of file diff --git a/data/38/DD/CB/38DDCB2134E250C78DB0705066E19F2F.xml b/data/38/DD/CB/38DDCB2134E250C78DB0705066E19F2F.xml new file mode 100644 index 00000000000..0c9f07829cf --- /dev/null +++ b/data/38/DD/CB/38DDCB2134E250C78DB0705066E19F2F.xml @@ -0,0 +1,271 @@ + + + +Two new diatom species of the genus Gomphonemopsis (Bacillariophyceae) from the coast of China and two new combinations for the genus + + + +Author + +Li, Lang +https://orcid.org/0000-0001-5649-1097 +Guangxi Key Laboratory of Marine Environmental Science, Guangxi Academy of Marine Sciences, Guangxi Academy of Sciences, Nanning 530007, China & Beibu Gulf Marine Industry Research Institute, Fangchenggang 538000, China + + + +Author + +Nong, Qun-Zhuan +https://orcid.org/0009-0004-6646-1528 +School of Resources, Environment and Materials, Guangxi University, Nanning 530004, China + + + +Author + +Chen, Chang-Ping +https://orcid.org/0000-0002-3332-2458 +School of Life Sciences, Xiamen University, Xiamen 361102, China + + + +Author + +Li, Yu-Hang +https://orcid.org/0000-0002-5546-1774 +Laboratory of Marine Organism Taxonomy and Phylogeny, Qingdao Key Laboratory of Marine Biodiversity and Conservation, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China +liyuhang@qdio.ac.cn + + + +Author + +Lai, Jun-Xiang +https://orcid.org/0000-0002-7139-1454 +Guangxi Key Laboratory of Marine Environmental Science, Guangxi Academy of Marine Sciences, Guangxi Academy of Sciences, Nanning 530007, China & Beibu Gulf Marine Industry Research Institute, Fangchenggang 538000, China +jxlai@gxas.cn + +text + + +PhytoKeys + + +2024 + +2024-03-26 + + +239 + + +255 +266 + + + + +http://dx.doi.org/10.3897/phytokeys.239.114018 + +journal article +http://dx.doi.org/10.3897/phytokeys.239.114018 +1314-2003-239-255 +FE69A71558BB587393ACD7593ABE7DE3 + + + + +Gomphonemopsis nana Lang Li, Yuhang Li & Junxiang Lai +sp. nov. + + + + +Fig. 1A-P + + + +Type materials. + + +Holotype +. + +Slide MBMCAS286906 deposited in the Marine Biological Museum, Chinese Academy of Sciences (MBMCAS), Qingdao, China. + + + +Iconotype +. + +Fig. +1K +. + + + +Type locality. + +Qingdao Bay, Qingdao City, the Yellow Sea ( +36°3'33.45"N +, +120°18'56.26"E +). Collected from the blades of seagrass + +Zostera marina + +by Lang Li, 11 October 2022. + + + +Description. + +LM +(Fig. +1A-J +). Valves linear, heteropolar with obtusely rounded head pole and sub-acutely rounded foot pole, 4.0-7.4 +μm +long, 1.1-1.5 +μm +wide. Axial area very narrow. Raphe indistinguishable in LM. Central area hyaline, extended transapically, or occasionally asymmetrical because of the presence of a stria on primary side of the valve (Fig. +1A +). Transapical striae sub-parallel throughout, except slightly radiate at apices, 26-30 in 10 +μm +. + + + +Figure 1. + +Gomphonemopsis nana + +A-J +light micrographs (differential interference contrast, DIC) +K-P +scanning electron micrographs +K +external view of an entire valve with hymenes covering areolae, iconotype specimen +L +external view of an entire valve without hymenes covering areolae, note the girdle bands perforated with two rows of pores (white arrowhead) +M +external detail of the central area, note the presence of two areolae on the primary side (white arrows) +N +external detail of the foot pole +O +internal view of an entire valve +P +internal detail of the central area. Scale bars: 5 +μm +( +A-J +); 1 +μm +( +K-O +); 0.5 +μm +( +P +). + + + +SEM +(Fig. +1K-P +). Externally, each stria composed of two elongate to round areolae, one on the valve face, the other on the mantle. A row of areolae presented around apices (Fig. +1K +). Areolae occluded by hymenes and becoming smaller towards the foot pole (Fig. +1K +). Raphe central, more or less straight (Fig. +1K, L +). Proximal raphe endings expanded, pore-like, and deflected in the same direction (Fig. +1K, M +). Distal raphe endings slightly expanded and terminating on the valve face (Fig. +1K, L +). Central area expanded transapically to the valve margin, but two areolae occasionally present on primary side (Fig. +1M +, white arrow). Girdle bands perforated with a double row of pores (Fig. +1L +, white arrowhead). Internally, areolae smaller and rounder than external ones (Fig. +1O +). Central area slightly elevated. Proximal raphe endings bent to the same side (Fig. +1P +) distal raphe endings terminate in small helictoglossae (Fig. +1O +). + + + +Etymology. + +The Latin adjective + +Gomphonemopsis nana + +refers to the tiny dimensions of the new species as compared to other + +Gomphonemopsis + +species. + + + +Distribution and ecology. + + +Gomphonemopsis nana + +is an epiphytic species known only from the type locality, where it occurs mainly in the low intertidal region at a temperature of 23.3 °C. The water salinity here was about 30 psu during sampling. Other species that were observed in the same sample include + +Amphora + +spp., + +Navicula + +spp., + +Nitzschia + +spp., + +G. exigua + +( +Kuetzing +) Medlin, + +Licmophora californica + +Grunow, + +Tabularia parva + +( +Kuetzing +) D.M.Williams & Round, + +T. fasciculata + +(C.Agardh) D.M.Williams & Round, + +Berkeleya rutilans + +(Trentepohl ex Roth) Grunow, + +Cocconeis scutellum + +Ehrenberg and + +Seminavis robusta + +Danielidis & D.G.Mann. + + + +PhycoBank registration. +http://phycobank.org/104208. + + + \ No newline at end of file diff --git a/data/38/DD/CC/38DDCC77E08B56E98AD383390FFB49FC.xml b/data/38/DD/CC/38DDCC77E08B56E98AD383390FFB49FC.xml new file mode 100644 index 00000000000..72d4bb2cbb1 --- /dev/null +++ b/data/38/DD/CC/38DDCC77E08B56E98AD383390FFB49FC.xml @@ -0,0 +1,415 @@ + + + +A taxonomic revision of Keraunea, including three new species and its phylogenetic realignment with Ehretiaceae (Boraginales) + + + +Author + +Moonlight, Peter W. +https://orcid.org/0000-0003-4342-2089 +Botany Department, School of Natural Sciences, Trinity College Dublin, Dublin 2, Ireland +p.moonlight@rbge.ac.uk + + + +Author + +Cardoso, Domingos Benicio Oliveira Silva +https://orcid.org/0000-0001-7072-2656 +Instituto de Pesquisas Jardim Botanico do Rio de Janeiro, Rio de Janeiro, Brazil & Universidade Federal da Bahia, Salvador, Bahia, Brazil + +text + + +PhytoKeys + + +2023 + +2023-02-20 + + +219 + + +145 +170 + + + + +http://dx.doi.org/10.3897/phytokeys.219.101779 + +journal article +http://dx.doi.org/10.3897/phytokeys.219.101779 +1314-2003-219-145 +A2ECEB672C4D5027A90252D384FB1795 + + + + +3. +Keraunea capixaba Lombardi, Phytotaxa 181: 54. 2014. + + + + +Fig. 5 + + + + +Type +. + + + + +Brazil +. + +Espirito +Santo + + +: Mun. +Jaguare +, perto + +da + +Comunidade +Sao +Jorge de +Padua + + +, sentido para + +Fatima + +, +18°54'29.0"S +, +40°8'44.9"W +, +26 Sep. 2013 +, + +G.S. Siqueira +891 + +( +holotype +: CVRD [acc. # 14565]; isotypes HRCB [acc. # 76196], SP [ +SP003725 +]) + +. + + + +Description. + +Scandent shrub or liana, to ca. 4 m. Stems cylindrical, hollow, 2-4 mm in diameter, glabrescent, rarely branching, internodes 2.4-11.5 cm long; side shoots 1.3-5.5 cm long, glabrescent. Leaves of main stem with the blades 7.0-13.5 +x +2.1-4.5 cm, elliptic, glabrescent, the venation pinnate, camptodromous, with 4-6 secondary veins; the base cuneate, the margins entire, ciliate, the apex attenuate; petioles 5-6.5 mm long, straight. Side shoots with 4-6 leaves, these progressively larger along the shoot; blades 1-9.5 +x +0.5-6.5 cm, ovate, rarely obovate or broadly ovate, glabrescent, the venation as on leaves of the main stem, the base cuneate to rounded, the margins entire, rarely crenulate toward the apex ( +Siqueira 891 +), ciliate, the apex acute to rounded; petioles 5.5-12 mm long, straight, glabrescent. Inflorescence corymbose, with 2-4 flowers; free portion of the pedicel, 8-14 mm long, 1.8-2.6 cm long, the remainder adnate to the bracteole, sericeous-pubescent with silky hairs; bracteole 3.3-3.5 +x +1.9-2.4 cm, inserted ca. +1/2 +of the way along the pedicel or rarely lacking, ovate, glabrescent, the venation as the leaves, the base short acute, margin entire, not ciliate, the apex acute. Flowers 5-merous. Calyx with the tube campanulate, ca. 3.5 mm long, the lobes 6.5-18 +x +1.5-2.5 mm, ensiform, glabrescent to minutely pubescent. Corolla with the tube campanulate, ca. 6.5 mm long, the lobes 19-26 +x +7.5-11.5 mm, elliptic to oblong, glabrous. Stamens epipetalous, inserted at the base of the corolla tube, the filaments 2-3 mm long, the anthers ca. 9 mm long, connective extending to 3.2 mm. Ovary subglobose, 2-locular, the locules biovulate; style single, conduplicate, unbranched; stigmas 2, truncate. Fruit inserted on the accrescent bracteole; calyx persistent, expanding to 18 mm long. + + + +Figure 5. +Morphology of + +Keraunea capixaba + +Lombardi +A +habit +B +inflorescence, front view +C +inflorescence, side view. For photograph of fruit with accrescent bracteole see +Lombardi (2014) +. All photographs by Geovane Siqueira. + + + + +Distribution. + +Endemic to +Espirito +Santo state and known from the municipalities of +Jaguare +, Sooretama and Nova +Venecia +(Fig. +2 +). + + + +Habitat. + +Collections of + +Keraunea capixaba + +have primarily been made in "mata tabuleiro" or flat, semi-deciduous forests found within the coast of the Mata +Atlantica +domain of Brazil. A more recent collection ( +Gurtler & Dutra 371 +) was made growing over rocks in forest understory at the base of a granitic outcrop. Specimen labels describe the species as scandent or lianescent. + + + +Conservation status. + + +Keraunea capixaba + +was provisionally assessed by +Lombardi (2014) +as Endangered because it was at that time known from four collections made within disturbed forest patches adjacent to the Sooterama Biological Reserve. We add five collections to the known distribution, including one collected within the Sooterama Biological Reserve ( +Covre s.n. +), two collected at the base of inselbergs> 30 km from the reserve ( +Gurtler & Dutra 371 +, +Demuner et al. 3799 +), and a gathering made a remarkable 500 km to the north near +Ipaui +, Bahia. The species is now known from six localities with a collective Extent of Occurrence (EOO) of ca. 11,000 km2. The species is known from <10 localities and has a EOO of <20,000 km2, so we assess + +K. capixaba + +as Vulnerable (VU B1 a b iii) under IUCN criteria ( +IUCN 2019 +). + + + +Etymology. + +The epithet is an indigenous term referring to people or objects from +Espirito +Santo state. + + + +Identification notes. + + +Keraunea capixaba + +is most morphologically and ecologically similar to the newly described + +K. velutina + +, the two species of the genus that are associated with more humid settings in the Mata +Atlantica +phytogeographic region, yet they were never found growing sympatrically. + +Keraunea capixaba + +differs in lacking an indumentum on the stems, side shoots and lower leaf surface (versus a velutinous-pubescent in + +K. velutina + +), and its ovate leaves on the side shoots (versus elliptic to narrowly-lanceolate). Its range is close to that of + +K. confusa + +, from which it is readily distinguished by its camptodromous venation (versus brochidodromous). + + + +Additional specimens examined. + + + +Brazil +. +Bahia + +: +Rod Ipiau-Ibirataia +, [ +14°6'S +, +39°41'W +], +13 Nov. 1971 +, + +T.S. Santos +2139 + +(HUEFS) + +. + + + +Espirito +Santo + + +: Mun. Sooretama, + +Reserva +Biologica +de Sooretama + +, [ +19°1'S +, +40°7'W +], +19 May 2015 +, + +C. Covre +s.n. + +(SAMES [SAMES03696]); Mun. +Rio Bananal +, +Alto Bananal +, +19°14'56"S +, +40°24'59"W +, + +300-600 m + +alt., +25 Apr. 2007 +, + +V. Demuner +et al. 3799 + +(BHCB [BHCB017211]); Mun. +Jaguare +, + +Perto da Comunidade +Sao +Jorge de +Padua + +, +25 Sep. 2013 +, + +D.A. Folli +7117 + +(CVRD [acc. #14563]; HRCB [acc. #16194], NY [02687787], RB [00895205]); Mun. Sooretama, Barro Roxo a +Corrego +Rodrigues, +19°4'35"S +, +40°13'25"W +, + +156 m + +alt., +8 Oct. 2014 +, + +D.A. Folli +7273 + +(CVRD [acc. #15122]; RB [01103439]); + +Mun. Nova +Venecia + +, fazenda +Santa Rita +, ao +pe +da pedra da torre (P3), +18°47'7"S +, +40°26'29"W +, +2 Feb. 2018 +, + +J. Gurtler +& +S.C. Dutra +371 + +(VIES [VIES036853]); +Mun. Sooretama +, +Rodovia ES +358, distrito +de Bom Jardim +, +19°2'20.31"S +, +40°14'48.23"W +, +1 Sep. 2012 +, + + +A. +Moreira de Assis + +& +J. Freitas +3340 + +(HRCB [acc. #76193], MBML [2 sheets: MBML00016754, MBML00016755]); + +Mun. +Jaguare + +, perto + +da + +Comunidade +Sao +Jorge de +Padua + + +, +18°54'29.0"S +, +40°8'44.9"W +, +6 Oct. 2013 +, + +G.S. Siqueira +893 + +(CVRD [acc. #14570], HRCB [acc. #76199], K [K001275507], MBML [MBML00016491], NY [02687786], RB [00895202]) + + + + + \ No newline at end of file diff --git a/data/38/DD/F8/38DDF807F32A7D4330A12EF3DE4013B9.xml b/data/38/DD/F8/38DDF807F32A7D4330A12EF3DE4013B9.xml new file mode 100644 index 00000000000..261c4c77d62 --- /dev/null +++ b/data/38/DD/F8/38DDF807F32A7D4330A12EF3DE4013B9.xml @@ -0,0 +1,86 @@ + + + +An annotated checklist of the chrysidid wasps (Hymenoptera, Chrysididae) from China + + + +Author + +Rosa, Paolo +Via Belvedere 8 / d, I- 20881 Bernareggio (MB), Italy + + + +Author + +Wei, Na-sen +Department of Entomology, College of Natural Resources and Environment, South China Agricultural University, Guangzhou 510640, China + + + +Author + +Xu, Zai-fu +Department of Entomology, College of Natural Resources and Environment, South China Agricultural University, Guangzhou 510640, China + +text + + +ZooKeys + + +2014 + +2014-11-19 + + +455 + + +1 +128 + + + + +http://dx.doi.org/10.3897/zookeys.455.6557 + +journal article +http://dx.doi.org/10.3897/zookeys.455.6557 +1313-2970-455-1 +7346B2B940BF4358AFE4B3F30023F9F2 +FF9EFF935938FF8EFF4DFFEBFFAEFF82 +578622 + + + + +120. +Chrysis illecebrosa Semenov-Tian-Shanskij, 1967 +Plate 42 + + + + + +Chrysis +(Tetrachrysis) illecebrosa + +Semenov-Tian-Shanskij, 1967: 166. Holotype ♂, North China [= Xinjiang]: Bugas near Hami [Kumul] (166 (descr.), depository: ZIN)*. + + +Chrysis illecebrosa +: +Kimsey and Bohart 1991 +: 421 (North China, cat., +comparata +group). + + + +Distribution. +China (Xinjiang). + + + \ No newline at end of file diff --git a/data/38/DE/22/38DE22B046CC59B891512366D1C02FFC.xml b/data/38/DE/22/38DE22B046CC59B891512366D1C02FFC.xml new file mode 100644 index 00000000000..e64555ebed1 --- /dev/null +++ b/data/38/DE/22/38DE22B046CC59B891512366D1C02FFC.xml @@ -0,0 +1,591 @@ + + + +A new deep-sea species of Elliptiolucina Cosel & Bouchet, 2008 (Bivalvia, Lucinida, Lucinidae) from cold seep of the South China Sea + + + +Author + +Jiao, Yingyi +Laboratory of Marine Organism Taxonomy and Phylogeny, Qingdao Key Laboratory of Marine Biodiversity and Conservation, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China & University of Chinese Academy of Sciences, Beijing 100049, China + + + +Author + +Wang, Minxiao +Laboratory of Marine Organism Taxonomy and Phylogeny, Qingdao Key Laboratory of Marine Biodiversity and Conservation, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China + + + +Author + +Guo, Yang +Laboratory of Marine Organism Taxonomy and Phylogeny, Qingdao Key Laboratory of Marine Biodiversity and Conservation, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China + + + +Author + +Zhang, Junlong +https://orcid.org/0000-0003-3831-4673 +Laboratory of Marine Organism Taxonomy and Phylogeny, Qingdao Key Laboratory of Marine Biodiversity and Conservation, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China +zhangjl@qdio.ac.cn + +text + + +Zoosystematics and Evolution + + +2023 + +2023-03-27 + + +99 + + +1 + + +261 +271 + + + + +http://dx.doi.org/10.3897/zse.99.101795 + +journal article +http://dx.doi.org/10.3897/zse.99.101795 +1860-0743-1-261 +150C3C31AF2847148B9A96A17424DDB5 +CF445D50EC925C63AFA7A19A2AAFFD3C + + + + +Elliptiolucina subovalis +sp. nov. + + + + +Figs 2 +, 3 +, 4F + + + +Material examined. + + + +Holotype + +: MBM229033, one complete specimen collected on +Aug. 3, 2018 +, by a TV grab, deposited in the +Marine Biological Museum +, +Chinese Academy of Sciences +(MBMCAS), Qingdao. + + + + +Description. +Shell medium-sized, 44.7 mm long, thick, elongate (SH/SL 0.78), sub-rectangular oval, inequilateral, nearly equivalve, slightly inflated (SW/SL 0.44). Umbones slightly prominent and prosogyrous, situated in front of the vertical midline, anterior umbonal slope slightly concave, postero-dorsal margin straight. Anterior margin narrowly rounded, posterior margin broad, rounded-truncate, and the vertical part slightly convex. Postero-dorsal corner obtuse. Ventral margin broadly rounded but slopes distinctly upswept in front. + + +Figure 2. + +Elliptiolucina subovalis + +sp. nov. +A, B. +Exterior and interior of the right valve; +C, D. +Exterior and interior of the left valve; +E. +Dorsal view; +F, G. +Detail of the hinge of the right and left valves. + + + +Shell white, flaky periostracum pale-brownish, dense, and slightly wrinkled towards the margin of the shell. Exterior with dense, irregular commarginal growth ribs, fine commarginal striae, and few irregular vertical lines which diverge from the commarginal sculpture and running in a more upward direction on the postero-dorsal area (Fig. +3A +), visible on 5 +x +magnification. Both of anterior and posterior dorsal area with one very slight radial depression. Lunule rather long, generally symmetrical, deeply sunken, lanceolate. Escutcheon long, completely covered by ligament which almost occupies the whole postero-dorsal margin and situated on a strong nymph. + + + +Figure 3. +Shell sculptures of + +Elliptiolucina subovalis + +sp. nov. +A. +Posterior surface (~5 +x +); +B. +Anterior surface (~5 +x +); +C. +Middle surface (~5 +x +). + + +Inner shell surface dull white to slightly orange inside pallial line, and glossy at the margin. Dense radial stria from umbonal cavity to the shell margin. Hinge plate narrow, with only very faint and low indications of cardinal teeth in both valves, but a strong anterior lateral tooth in right valve, and a corresponding socket in left valve. Anterior adductor scar elongate, detached from pallial line for less than 1/2 of length. A distinct but shallow pedal retractor scar above the anterior adductor scar. Posterior adductor scar reniform, with a dorsal notch, open to the anterior. Pallial line entire. Shell margin smooth. + + +Etymology. + +The specific name + +Elliptiolucina subovalis + +was derived from the Latin +sub ++ +oval +in reference to the shape of the shell, sub-rectangular oval but more ovate than most congeners. + + + +Type locality. + +An active seepage site ( +22.1159°N +, +119.2854°E +), site F, in southwest Taiwan, South China Sea, 1146 m depth (Fig. +1 +). Buried in the muddy bottom near the seep. + + + +Remarks. + +The new species possesses thick, elongated shells with fine commarginal sculptures, a relatively short anterior adductor muscle scar, and a narrow hinge, especially a dorsal notch in the posterior adductor scar, which are in accord with the key characteristics of +Myrteinae +. It corresponds to the genus + +Elliptiolucina + +in the elongated shells and fine irregular commarginal sculptures. The new species was found from IWP. The West-Atlantic genus + +Jorgenia + +shares similar general morphology of the outer shell with + +Elliptiolucina + +. But the limited distribution combined with the different hinge features (small but distinct cardinal teeth in both valves of + +Jorgenia + +) can differentiate the two genera. + + + +Elliptiolucina subovalis + +sp. nov. is distinct from other congeners by possessing a strong anterior lateral tooth on the right valve and anterior tapering, subrectangular-oval shells (Table +1 +, Fig. +4 +). The new species is morphologically similar to + +E. magnifica + +Cosel & Bouchet, 2008 in outline but can be distinguished by the more prominent and prosogyrous umbones and the lateral tooth. + +Elliptiolucina subovalis + +sp. nov. is the second species after + +E. williamsae + +known to possess a lateral tooth. The distinct cardinal teeth of + +E. williamsae + +can be used to separate it from the new species. In addition, the tapering anterior shell of + +E. subovalis + +differentiates the two species. + +E. virginiae + +Cosel & Bouchet, 2008 can be distinguished from the new species by its almost rectangular outline. It has a straight dorsal margin and vertical posterior margin, while the shell shape of + +E. subovalis + +sp. nov. is rather subovate. The more compressed shells of + +E. virginiae + +(SW/SL ratio = 26-29%) and + +E. labeyriei + +Cosel & Bouchet, 2008 (SW/SL ratio = 24-33%) are distinct from that of + +E. subovalis + +sp. nov. (SW/SL ratio = 44%). + +E. ingens + +can be separated from the new species by its ridges in the inner surface running from the umbonal cavity to both posterior and anterior adductor scars and the absence of a posterior dorsal corner on the external surface. + + + +Figure 4. +Outline drawing of shells interiors of + +Elliptiolucina + +. +A. + +E. magnifica + +; +B. + +E. labeyriei + +; +C. + +E. virginiae + +; +D. + +E. ingens + +; +E. + +E. williamsae + +; +F. + +E. subovalis + +sp. nov. Sketches of +A-E. +were adapted from Kuhara (2014, fig. 4) and +Glover and Taylor (2016 +, figs 19, 20). + + + + +Table 1. +Comparison of conchological features in all species of the genus + +Elliptiolucina + +. Modified by Kuhara (2014). Additional information was adapted from +Cosel and Bouchet (2008) +; +Okutani (2011) +; +Glover and Taylor (2016) +. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
- + +E. ingens + + + +E. magnifica + + + +E. labeyriei + + + +E. virginiae + + + +E. williamsae + + + +E. subovalis + +sp. nov. +
Outlineoval, somewhat discoidsubrectangular-ovalsubrectangular-ovalsub-rectangularsubovatesubrectangular-oval
Shell length (mm)53.2-98.480.418.5-43.623.0-78.520.5-44.144.7
SH/SL ratio72-84%72%68-80%63-69%78-86%78%
SW/SL ratio29-45%38%27-33%26-29%36-44%44%
Umbonestumid and lowsmall and flattenedflattenedsmalllowslightly prominent
Hinge teethedentulousedentulousoccasionally cardinal tooth indicationsedentuloussmall cardinal teeth and lateral teethcardinal tooth indications and lateral teeth
Width of lunulenarrownarrowvery narrowvery narrownarrownarrow
Length of lunulerather long to longrather longlongshort-long
LL/SL ratio22-30%ca. 22%ca. 25%ca. 14%-ca. 25%
Outline of posterodorsal cornerroundangularrather angularangularangularangular
Position of posterodorsal cornerlowhighslightly lowhighslightly lowslightly low
+
+
+ +Molecular analysis. + +The obtained sequences were uploaded in GenBank (see Suppl. material 1). The entire dataset included sequences of 219 individuals from 146 species. Because markers are not always available for the same species, somewhat different taxon sets are employed in three-gene and 18S trees. In particular, for + +E. williamsae + +, only the 18S rRNA gene was available. Phylogenetic frameworks of ML and BI methods showed similar topologies on each dataset. Thus, four trees were presented in two summary cartoon trees in our study (Figs +5 +, +6 +). Our results based on three-gene (Fig. +5 +) have divided the species of +Lucinidae +into seven clades, corresponding to seven subfamilies. Phylogenetic results of two datasets displayed similar topologies within +Myrteinae +. Our new species + +Elliptiolucina subovalis + +sp. nov. was found to be a member of +Myrteinae +. + +E. williamsae + +and + +E. subovalis + +sp. nov. formed a stable sister group in 18S trees. A close relationship between the group + +E. subovalis + +sp. nov. (+ + +E. williamsae + +) and + +Rostrilucina garuda + +Cosel & Bouchet, 2008 was shown in all trees. The new species formed a sister clade of all other +Myrteinae +species in conjunction with + +Rostrilucina garuda + +and + +Myrtea flabelliformis + +(Prashad, 1932) in concatenated trees. In 18S trees, the three species mentioned above, together with the + +E. williamsae + +, were also basal to other +Myrteinae +species. The monophyletic + +Elliptiolucina + +and + +Myrtea + +were not supported. + +E. ingens + +involved in a clade composed of + +Gloverina + +Cosel & Bouchet, 2008, + +Myrtea catonii + +(Glover & J. D. Taylor, 2016), + +Myrtea vincentia + +(Glover & J. D. Taylor, 2007), and another undescribed + +Myrtea + +species in all trees. Deep-sea species of +Myrteinae +formed three monophyletic clades in the concatenated dataset (Fig. +5 +). Two stable monophyletic deep-sea clades (clade A and C) represented by species of + +Elliptiolucina + +, + +Gloverina + +, + +Myrtea + +and + +Rostrilucina + +Cosel & Bouchet, 2008. The polyphyletic genus + +Elliptiolucina + +and + +Myrtea + +were shared in the two clades. One species of + +Taylorina + +Cosel & Bouchet, 2008, + +T. solomonensis + +Cosel & Bouchet, 2008, formed a separate clade, as the sister group of clade A plus all of shallow-sea +Myrteinae +. + + + +Figure 5. +Phylogenetic tree inferred by Maximum likelihood (ML) and Bayesian inference (BI) based on concatenated dataset of 18S, 28S and CytB genes. The species marked with an inverted triangle are deep-sea species. + + + + +Figure 6. +Phylogenetic tree inferred by Bayesian inference (BI) and Maximum likelihood (ML) based on 18S rRNA gene. + + + +
+
\ No newline at end of file diff --git a/data/38/DE/59/38DE590873FC0697C6674F688D803E37.xml b/data/38/DE/59/38DE590873FC0697C6674F688D803E37.xml new file mode 100644 index 00000000000..6533ed1172b --- /dev/null +++ b/data/38/DE/59/38DE590873FC0697C6674F688D803E37.xml @@ -0,0 +1,61 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828--9042 + + + + +Cryptus obscuripes Zetterstedt, 1838 + + + + +borealis +Thomson, 1873 preocc. + + +carpathicus +Szepligeti +, 1916 + + + +Distribution +England + + +Notes +BMNH, det. Schwarz, added here + + + \ No newline at end of file diff --git a/data/38/DE/E7/38DEE70CCC3BDA52224358B69103D4F9.xml b/data/38/DE/E7/38DEE70CCC3BDA52224358B69103D4F9.xml new file mode 100644 index 00000000000..87963aeccad --- /dev/null +++ b/data/38/DE/E7/38DEE70CCC3BDA52224358B69103D4F9.xml @@ -0,0 +1,104 @@ + + + +A survey of the family Carabodidae C. L. Koch, 1836 (Acari: Oribatida) + + + +Author + +Mahunka, S. + +text + + +Acta Zoologica Hungarica + + +1986 + +32 + + +73 +135 + + + + +http://unknown + +journal article +ORI5666 +8A93F5C4-1ED6-4698-8284-1B31E250AF9D + + + + +CARABODINAE +, C. L. Koch, 1836 + + + +Diagnosis: Prodorsum without high elevations or protuberances, notogaster without any structure. Lamellae normal, running marginally. Dorsosejugal region normal, both parts of body flat or gradually becoming convex, without structure. + + + +Typus generis: +Carabodes +C. L. Koch, 1836 + +Other genera: + +Aokiella +Balogh et Mahunka, 1967 + + +Austrocarabodes +Hammer, 1966 + + +Cavernocarabodes +Mahunka, 1974 + + +Flexa Kuliev +, 1977 + + + +Gymnobodes + +Balogh, 1965 + + +Klapperiches Mahunka +, 1974 + + +Odontocepheus +Berlese, 1913 + + +Pentabodes +P. Balogh, 1984 + + +Phyllocarabodes +Balogh et Mahunka, 1969 + + +Tansocepheus Mahunka +, 1983 + + +Trichocarabodes +Balogh, 1961 + + +Uluguroides Mahunka +, 1983 + + + + \ No newline at end of file diff --git a/data/38/DE/EE/38DEEE34D793582DED0EC0389000F484.xml b/data/38/DE/EE/38DEEE34D793582DED0EC0389000F484.xml new file mode 100644 index 00000000000..3df1f1f83a4 --- /dev/null +++ b/data/38/DE/EE/38DEEE34D793582DED0EC0389000F484.xml @@ -0,0 +1,84 @@ + + + +Polychaetes of Greece: an updated and annotated checklist + + + +Author + +Faulwetter, Sarah + + + +Author + +Simboura, Nomiki + + + +Author + +Katsiaras, Nikolaos + + + +Author + +Chatzigeorgiou, Giorgos + + + +Author + +Arvanitidis, Christos + +text + + +Biodiversity Data Journal + + +2017 + +5 + + +20997 +20997 + + + + +http://dx.doi.org/10.3897/BDJ.5.e20997 + +journal article +http://dx.doi.org/10.3897/BDJ.5.e20997 +1314-2828--20997 + + + + +Subadyte pellucida (Ehlers, 1864) + + + + +Adyte pellucida +(Ehlers, 1864) | +Scalisetosus fragilis +( +Claparede +, 1868) | +Scalisetosus pellucidus +(Ehlers, 1864) | +Subadyte pellucida +(Ehlers, 1864) + + + +Notes +Type locality: Mediterranean (Adriatic). + + + \ No newline at end of file diff --git a/data/38/DF/1A/38DF1A66A08231B3D9180686643011BC.xml b/data/38/DF/1A/38DF1A66A08231B3D9180686643011BC.xml new file mode 100644 index 00000000000..745cce102c5 --- /dev/null +++ b/data/38/DF/1A/38DF1A66A08231B3D9180686643011BC.xml @@ -0,0 +1,74 @@ + + + +Checklist of bees (Hymenoptera: Apoidea) from managed emergent wetlands in the lower Mississippi Alluvial Valley of Arkansas + + + +Author + +Stephenson, Phillip L + + + +Author + +Griswold, Terry L + + + +Author + +Arduser, Michael S + + + +Author + +Dowling, Ashley P G + + + +Author + +Krementz, David G + +text + + +Biodiversity Data Journal + + +2018 + +6 + + +24071 +24071 + + + + +http://dx.doi.org/10.3897/BDJ.6.e24071 + +journal article +http://dx.doi.org/10.3897/BDJ.6.e24071 +1314-2828-6-24071 + + + + +Lasioglossum (Dialictus) pilosum (Smith, 1853) + + + +Notes + +New species record for Arkansas. Occurs over much of the eastern US ( +Gibbs 2011 +). Opportunistic (Table 1: All Sites). + + + + \ No newline at end of file diff --git a/data/38/DF/69/38DF699A5A82B805B4303FF5C70057A3.xml b/data/38/DF/69/38DF699A5A82B805B4303FF5C70057A3.xml new file mode 100644 index 00000000000..ed1cf5b6be0 --- /dev/null +++ b/data/38/DF/69/38DF699A5A82B805B4303FF5C70057A3.xml @@ -0,0 +1,199 @@ + + + +Flora Helvetica - Rosaceae + + + +Author + +Konrad Lauber + + + +Author + +Gerhart Wagner + + + +Author + +Andreas Gygax + +text + + +2018 +Haupt Verlag + +Bern + + + +Flora Helvetica + + + +234 +314 + + + +book chapter +978-3-258-08047-5 + + + + + +Fragaria vesca +L. + + + + + +Artbeschreibung: +5-20 cm +hoch, + +mit langen oberirdischen +Auslaeufern + +. +Grundstaendige +Blaetter +lang gestielt, 3teilig. +Teilblaetter +2-5 cm +lang, +verkehrt-eifoermig +, am Grund +keilfoermig +, +gezaehnt +, + +Endzahn nicht kleiner als die benachbarten +Zaehne +. +Blueten +weiss + +, zwittrig, Durchmesser +1-1,8 cm +, in +wenigbluetigem +, doldigem +Bluetenstand +. Haare der +Bluetenstiele +aufrecht oder anliegend. + +Frucht eine rote, fleischige, +suesse +Scheinbeere. Kelch an der reifen Frucht abstehend und nicht mit dieser abreissend + +. + + + + +Bluetezeit +: 4-6 + + +Standort und Verbreitung in der Schweiz: Lichte +Waelder +, +Waldraender +, Hecken / kollin-subalpin / CH + + + +Verbreitung global: Eurasiatisch + + + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +maessig +feucht +Lichtzahl LhalbschattigSalzzeichen--
Reaktionszahl Rschwach sauer bis neutral (pH 4.5-7.5)Temperaturzahl T +montan ( +Waelder +mit Buche, Weisstanne, in den Zentralalpen mit +Waldfoehre +) +
+Naehrstoffzahl +N + +maessig +naehrstoffarm +bis +maessig +naehrstoffreich + +Kontinentalitaetszahl +K + +subozeanisch bis subkontinental (mittlere Luftfeuchtigkeit, +maessige +Temperaturschwankungen und +maessig +tiefe Wintertemperaturen) +
+
+
+ + +Volksname Deutscher Name: +Wald-Erdbeere +Nom +francais +: +Fraisier des bois +Nome italiano: +Fragola comune + + +
+
\ No newline at end of file diff --git a/data/38/DF/BF/38DFBFF28DB8477F8BCB093F21FDDAFE.xml b/data/38/DF/BF/38DFBFF28DB8477F8BCB093F21FDDAFE.xml new file mode 100644 index 00000000000..e0343ddb5c0 --- /dev/null +++ b/data/38/DF/BF/38DFBFF28DB8477F8BCB093F21FDDAFE.xml @@ -0,0 +1,87 @@ + + + +Checklist of Fishes from Madagascar Reef, Campeche Bank, Mexico + + + +Author + +Zarco Perello, Salvador + + + +Author + +Moreno Mendoza, Rigoberto + + + +Author + +Simoes, Nuno + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1100 +1100 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1100 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1100 +1314-2828--1100 + + + + +Echeneis Linnaeus, 1758 + + + +Materials + + +Type status: +Other material +. Occurrence: recordedBy: +Salvador Zarco Perello +; individualCount: +1 +; Location: continent: America; country: +Mexico +; stateProvince: Yucatan; locality: +Madagascar Reef +; verbatimDepth: 5 m; verbatimLatitude: 780535.103072; verbatimLongitude: 2373588.16789; verbatimCoordinateSystem: UTM 15N; verbatimSRS: WGS84; decimalLatitude: +21.442888 +; decimalLongitude: +-90.293376 +; Event: samplingProtocol: +Photosampling +; eventDate: +24/9/2007 +; Record Level: collectionID: YUC-PEC_239-01-64; institutionCode: +UMDI-SISAL +; collectionCode: +CIRR + + + + +Distribution +Worldwide. + + + \ No newline at end of file diff --git a/data/38/E0/09/38E0099812E7513E6C4B07D490BA53F1.xml b/data/38/E0/09/38E0099812E7513E6C4B07D490BA53F1.xml new file mode 100644 index 00000000000..70b8cdbd85a --- /dev/null +++ b/data/38/E0/09/38E0099812E7513E6C4B07D490BA53F1.xml @@ -0,0 +1,185 @@ + + + +The genus Quartinia Ed. Andre, 1884 (Hymenoptera, Vespidae, Masarinae) in Southern Africa. Part IV. New and little known species with complete venation + + + +Author + +Gess, Friedrich W. + +text + + +Journal of Hymenoptera Research + + +2011 + +2011-03-10 + + +21 + + +1 +39 + + + + +http://dx.doi.org/10.3897/jhr.21.870 + +journal article +http://dx.doi.org/10.3897/jhr.21.870 +1314-2607-21-1 +AE1D69FBFB3A4ECFB3E08ED5B5E9AE5B +FFA3E36FB9245951FB58FF84FF913F2C +574747 + + + + +Quartinia namibensis +sp. n. +Figs 35-41 + + + +Holotype + +♀, NAMIBIA: Sperrgebiet, Klinghardtberge, +Tsabiam's +Camp (27.10S, 15.42E), 4.ix.2002 (F. W. and S. K. Gess) [AMG]. + + + +Paratypes. + +NAMIBIA: Sperrgebiet, Klinghardtberge, Nomitsas (27.27S, 15.52E), 31.viii.2002 (F. W. and S. K. Gess), ♀ (visiting yellow flowers of +Grielum sinuatum +Licht. ex Burch., +Neuradaceae +) [AMG]; NAMIBIA: Diamond Area 1: Roter Kamm (27.46S, 16.18E), 25-30.vi.1989 (C. S. Roberts), 2 ♂♂ [♂ NNIC; ♂ AMG]. + + + +Figures 35-41. +Quartinia namibensis +35 +♀, lateral view ( +x +10) +36 +♂, lateral view ( +x +12) +37 +♀, dorsal view ( +x +10) +38 +♂, dorsal view ( +x +12) +39 +♀, head, front view ( +x +14) +40 +♂, head, front view ( +x +16) +41 +♂, tergum VII, dorsal view ( +x +12). + + + + +Diagnosis. + +Large (4.8-5.4 mm). Fore wing with Cu1a and 2 +m-cu +complete and as thick as the other veins. Tegula whitish-yellow (other than for testaceous median area), with posterior inner corner inwardly produced and acute. Mesosoma and gaster black, richly marked with whitish-yellow. Metanotum of both sexes whitish-yellow. Male with striking and unique, long, pale, apically curved setae on ventral surface of flagellomeres 1-7, on labrum and on distal third of clypeus. + + + +Description. + +Female +( +Figs 35, 37, 39 +): Black. The following are various shades of whitish-yellow: underside of antenna; medially interrupted band on anterior margin of pronotum, carried down to and expanded in humeral area, and narrowly extended along hind margin to postero-dorsal angle; tegula (other than for testaceous median area); tri-lobed curved band on disk of scutellum (leaving a bi-lobed black basal area); entire scutellar lamella; metanotum; ill-defined small area dorsally on propodeum (in paratype only); posterior bands attaining sides and somewhat anteriorly widened medially and laterally on terga I - V. Reddish yellow are: narrow subapical posterior bands on sterna II - V; median part of mandible; apex of femur, tibia (except dark brown +streak +on fore tibia) and tarsus of all legs. Upper surface of antenna dark reddish-brown; wings sub-hyaline; stigma and veins light brown. + +Length 5.4 mm; length of fore wing 3.6 mm; hamuli 4. + +Head in front view 1.35 +x +as wide as long. POL: OOL = 1: 0.55. Clypeus, frons and vertex microreticulate (shagreened) with dense, small, shallow punctures (barely discernable on clypeus and lower half of frons, obvious on upper half of frons and on vertex). + + +Thorax semi-matt, distinctly microreticulate (shagreened) and punctured; punctures larger and more clearly defined than on head; interstices varying from less than puncture width to more than double puncture width. Tegula with posterior inner corner inwardly produced and acute. Fore wing with Cu1a and 2 +m-cu +complete and as thick as the other veins. + +Gaster moderately shiny, with small, indistinct punctures. + +Male +( +Figs 36, 38, 40, 41 +): Black.The following are various shades of whitish-yellow: antenna (except narrow ferruginous mark dorsally on scape, pedicel and proxi +mal +flagellomeres); mandible; labrum; clypeus; paraocular area (streak carried narrowly upwards from mandibular insertion into lower half of ocular sinus where slightly widened); large, median, dorsally bi-lobed marking on frons (extending from clypeo-frontal suture to level of top of ocular sinus); band on anterior margin of pronotum, carried down to and expanded in humeral area, and narrowly extended along hind margin to postero-dorsal angle; tegula (other than for testaceous median area); transverse, postero-median spot on scutellum; entire scutellar lamella; metanotum; posterior bands attaining sides and slightly anteriorly widened medially and laterally on terga I - VI. Reddish-yellow are: apex of femur, tibia (except dark brown streak on fore tibia) and tarsus of all legs. Wings sub-hyaline; stigma and veins light brown. + +Length circa 4.8 mm; length of fore wing 3.1 mm; hamuli 4. + +Head in front view 1.4 +x +as wide as long; POL: OOL = 1: 0.6. + +Surface sculpture of head, thorax and gaster as in female. Tegula as in female. Flagellomeres 1-7 ventrally, labrum, clypeus on distal third with long, pale, apically curved setae; length of setae on antennae approximating or exceeding width of proximal flagellomeres, that of setae on clypeus longer. Tergum VII somewhat depressed, apico-medially with a V-shaped slit; lobes flanking slit rounded. Sterna atuberculate. Parameres rounded apically, without a tooth. + + +Etymology. + +The name, +Quartinia namibensis +, an adjective, is derived from the Namib Desert, and refers to the provenance of the species. + + + +Geographic distribution. + +Known only from the Sperrgebiet (Diamond Area 1) of Namibia, that is from the Desert and Succulent Steppe (Winter rainfall area) of +Giess (1971) +. + + + +Floral associations. + +Grielum sinuatum +Licht. ex Burch.( +Neuradaceae +). + + + +Nesting. +Unknown. + + +Discussion. + +The two females from Nomitsas and +Tsabiam's +Camp (both localities in the Klinghardtberge) and the two males from Roter Kamm (below and south-west of the Aurusberg) are here associated on the basis of general similarity, allowance being made for secondary sexual differences. The association requires confirmation by the study of material of both sexes found flying together in one or more localities. + + + + \ No newline at end of file diff --git a/data/38/E0/31/38E0315C98261429F2EDCE76EBBD883B.xml b/data/38/E0/31/38E0315C98261429F2EDCE76EBBD883B.xml new file mode 100644 index 00000000000..ea2db6d747c --- /dev/null +++ b/data/38/E0/31/38E0315C98261429F2EDCE76EBBD883B.xml @@ -0,0 +1,63 @@ + + + +Descriptions de nouvelles fourmis éthiopiennes (quatrième note). + + + +Author + +Santschi, F. + +text + + +Revue de Zoologie et de Botanique Africaines + + +1928 + +16 + + +54 +69 + + + +journal article +3628 +10.5281/zenodo.18159 + + + + +17. - +Crematogaster (Acrocoelia) vidua +n. sp. + + + +[[ worker ]]. - Long. 4 mm. - Noire. Mandibules, antennes, col, articulations du pedoncule et tarses rouge sombre. Extreme bout du gastre jaunatre. Dessus de la tete et face occipitale luisante et presque lisse. Devant et cotes de la tete jusqu'aux cretes frontales finement stries en long. Une fine et dense striation longitudinale sur le dos du thorax dans l'intervalle de laquelle se place une fine ponctuation reticulaire. Sur les cotes du thorax c'est cette ponctuation qui predomine, surtout sur la mesopleure. Le pedoncule est aussi finement ponctue, sauf les angles anterieurs du petiole, et lisse. La moitie inferieure de la face declive de l'epinotum est tres lisse. Le gastre a son brillant attenue par une reticulation microscopique. Seulement quelques longs poils vers la bouche et le bout du gastre. Une pubescence dressee sur la tete, plus oblique sur le gastre et les appendices. + +Tete a peine plus large que longue, les cotes assez arques, le bord posterieur droit. Yeux faiblement convexe occupant le troisieme quart des cotes de la tete. Sillon frontal distinct jusqu'a la fossette ocellaire. Cretes frontales tres espacees, paraissant se prolonger jusqu'au niveau du tiers posterieur des yeux. Aire frontale etroite, striee, ses sutures laterales indistinctes, l'anterieure fortement imprimee. Epistome faiblement convexe sauf derriere ou il s'enfonce vers la suture, le centre lisse, les cotes faiblement stries. Mandibules striees. Le scape depasse a peine le bord posterieur de la tete. Articles 3 a 5 du funicule plus larges que longs, les 6 et 7 aussi longs qu'epais. Dernier article de la massue presque aussi long que les deux precedents reunis. Thorax assez svelte. Le pronotum a une bordure laterale distincte mais mousse et un peu relevee qui le rend un peu concave transversalement, mais plus faiblement que chez +andrei +For. Mesonotum carene et plat ou tres faiblement concave devant (concave et sans carene chez +andrei +), sa face declive peu concave. Sillon metanotal un peu moins profond que chez +andrei +. Face basale de l'epinotum convexe, environ un tiers plus large derriere que longue au milieu, plus etroite que chez +andrei +, passant par une convexite a la face declive. Epines droites, divergentes, longues comme la moitie de l'intervalle de leur base, a peine plus epaisse que chez +andrei +. Petiole comme chez cette derniere mais les cotes et les angles anterieurs plus releves, ce qui rend le disque plus concave. Postpetiole fortement sillonne au milieu. Du reste ressemblant fort a +andrei +dont elle differe surtout par son mesonotum et ses yeux bien plus grands. Se place entre +castanea +et +menileki +For. Cote d'Ivoire: Grand Bassam (H. Mottaz leg.). + + + + \ No newline at end of file diff --git a/data/38/E0/BE/38E0BE8B7F1D57B28D83CAC184CF274C.xml b/data/38/E0/BE/38E0BE8B7F1D57B28D83CAC184CF274C.xml new file mode 100644 index 00000000000..53ae45d90fe --- /dev/null +++ b/data/38/E0/BE/38E0BE8B7F1D57B28D83CAC184CF274C.xml @@ -0,0 +1,260 @@ + + + +Amphibian and reptilian fauna from the early Miocene of Echzell, Germany + + + +Author + +Vasilyan, Davit +https://orcid.org/0000-0001-8712-0678 +JURASSICA Museum, Route de Fontenais 21. 2900 Porrentruy, Switzerland & Department of Geosciences, University of Fribourg, Chemin du musee 6, 1700, Fribourg, Switzerland +davit.vasilyan@jurassica.ch + + + +Author + +Cernansky, Andrej +https://orcid.org/0000-0001-8920-2503 +Department of Ecology, Laboratory of Evolutionary Biology, Faculty of Natural Sciences, Comenius University in Bratislava, Mlynska dolina, Ilkovicova 6, 842 15 Bratislava, Slovakia + + + +Author + +Szyndlar, Zbigniew +Institute of Systematics and Evolution of Animals, Polish Academy of Sciences, Slawkowska 17, 31 - 016 Krakow, Poland + + + +Author + +Moers, Thomas +https://orcid.org/0000-0003-2268-5824 +Department of Palaeobiology, Swedish Museum of Natural History, P. O. Box 50007, 104 05 Stockholm, Sweden & Bolin Centre for Climate Research, Stockholm University, Stockholm, Sweden + +text + + +Fossil Record + + +2022 + +2022-05-10 + + +25 + + +1 + + +99 +145 + + + + +http://dx.doi.org/10.3897/fr.25.83781 + +journal article +http://dx.doi.org/10.3897/fr.25.83781 +2193-0074-1-99 +7A16698D4F1848D29D9651A6E0CC15AC +2F5D6AE2EEB55A17ACF1623B06B4EA8D + + + + +Pelobates sanchizi Venczel, 2004 + + + + +Fig. 7 + + + +Material. +Four frontoparietals HLMD-Ez 2107-2110, 13 squamosals HLMD-Ez 2104-2106, one premaxilla HLMD-Ez 2098, 48 maxillae HLMD-Ez 2095-2097, 38 fragments of skull bones HLMD-Ez 2103, three presacral HLMD-Ez 2098, 2099, 2102 and two sacral vertebrae HLMD-Ez 2100, 2101, 11 ilia HLMD-Ez 2111-2115. + + +Description. + +Frontoparietals: Fragmentarily preserved remains are covered dorsally with the characteristic pit-and-ridge style sculpture as well as low spines (Fig. +7A, H +). The tectum supraorbitale is moderately broad. In dorsal view, the lateral superior process is longer than broad. The articulation surface with the squamosal is well-developed, concave and oriented fully laterally (Fig. +7A +). Neither incrassation frontoparietalis nor the margins are preserved/observable in the remains. The paroccipital process is reduced, but its dorsal surface possesses a distinct crest. The medial base of the paroccipital process is pierced by the occipital arterial foramen, which is covered dorsally by the posterior margin of the frontoparietal and, thus, not visible in dorsal view (Fig. +7E +). The fragmentarily preserved parts of the inferior superior process suggest that it was not longer than the lateral superior process. However, its lateral and slightly ventrally bending can be assumed. The arteria orbitonasalis opens ventrally on the supraorbital tectum (Fig. +7F +). + + + +Figure 7. + +Pelobates sanchizi + +from the Echzell locality. Frontoparietals HLDM-Ez 2109 ( +A, B +), HLDM-Ez 2107 ( +C, D +), HLDM-Ez 2108 ( +E-G +). Squamosals HLDM-Ez 2105 ( +H, I +), HLDM-Ez 2106 ( +J, K +). Maxillae HLDM-Ez 2077 ( +L, M +), HLDM-Ez 2097 ( +N, O +). Premaxilla HLDM-Ez 2098 ( +P, Q +). Vertebrae HLDM-Ez 2101 ( +S-V +), HLDM-EZ 2099 (r). Ilia HLDM-Ez 2113 ( +W +), HLDM-Ez 2111 ( +X-Z +), HLDM-Ez 2112 ( +AA +). Bones figures in ( +A, C, E, G, H, J, U +) dorsal, ( +B, D, I, K, V +) ventral, ( +F, T, Y +) posterior, ( +L, N, P +) labial, ( +M, O, Q +) lingual, ( +S +) anterior, ( +R, W, X, AA +) lateral and ( +z +) medial views. Scale bars: 1 mm. + + + +Squamosals: The dorsal surface is covered by a similar to frontoparietal pit-and-ridge sculpture. The bone remains are fragmentarily preserved. Only in HLMD-Ez 2105 (Fig. +7H, I +), an intact posterodorsal process lamina is present, and shows rounded posterior margin. The dorsal and zygomatic processes are broken. However, considering the presence of intact and concave bone margins between the preserved bases of these processes, we can suggest that they were delimited from each other. In ventral view, lamellar structures at the base of the posterolateral processes are observable (Fig. +7I, K +). However, they are incomplete for any further description. + + +Maxillae: The labial surface of the bone is covered by a dense network of moderately deep to deep pits-and-ridge sculpture. The distinct zygomatic process extends posterodorsally and has a rounded posterior tip (Fig. +5L +). The posterior process projects backwards. It is separated clearly from the zygomatic process by a deep concavity and projects much posteriorly. The orbital margin is concave. In lingual view, the pterygoid process projects posteromedially (Fig. +7M, O +). Anteriorly, it is connected with the dorsally oriented lamella above the horizontal lamina. + + +Premaxilla: In anterior view, the pars dentalis is low but broad. Its surface is covered by rugose structures (Fig. +7P +), which recalls the pit-and-ridge sculpture of, e.g., frontoparietal and maxilla. The pars facialis is broken, but its preserved base suggests a L-shaped form. Medially from this process, another shorter and posteromedially oriented process is present. The lateral crest (sensu +Venczel 2004 +) is moderately developed. The dental crest possesses 15 tooth pedicles (Fig. +7Q +). + + +Vertebrae: three presacral and two sacral vertebrae are present. The vertebra centrum is procoelous (four vertebrae, HLMD-Ez 2098, 2100-2102) or amphicoelous (one vertebra, HLMD-Ez 2099, Fig. +7R +). The HLMD-Ez 2099 represents a small-sized individual that, most probably, does not have fully ossified joints. In presacral vertebrae, the neural arch is high; and the neural canal is large. The foramina for the spinal nerve are present slightly above the posterior bases of the neural arch. In presacral vertebrae, they are visible in lateral view, whereas in sacral ones - in posterior views (Fig. +7T +). The sacral vertebrae have a broad and flattened transverse process. + + +Ilium: Though all ilia are very fragmentarily preserved, the following characters can be observed on the material: the acetabular region triangular; the acetabulum itself has round outline; the dorsal prominence low and covered by rare irregular structures; the dorsal protuberance absent; the moderately deep spiral groove extends from ventrolateral to dorsomedial direction in the region of the fusion of iliac shaft and acetabulum (Fig. +7W +-AA); in medial view, the ilioischiatic juncture is covered by elongated striae (Fig. +7Z +); the dorsal acetabular expansion larger than the ventral one. + + + +Remarks. + +The described remains can be assigned to the genus + +Pelobates + +based on the following combination of characters: 1) azygous frontoparietals articulating with the squamosals; 2) well-pronounced pit-and-ridge style sculpture with pustular structures on frontoparietal, squamosal and maxillae; 3) the presence of the spinal nerve foramina in vertebrae; 4) the presence of the moderately deep spiral groove on ilium, etc. (e.g., +Venczel 2004 +; + +Rocek +et al. 2014 + +). The fossil material of + +Pelobates + +can be allocated to the species + +P. sanchizi + +considering: 1) the presence of moderately broad tectum supraorbitale; 2) the occipital arterial foramen not visible in dorsal view; 3) the arteria orbitonasalis opening ventrally on the supraorbital tectum; 4) delimited posterior and posterodorsal processes of squamosal ( +Venczel 2004 +) + + +Comparison of our material with other fossil species of + +Pelobates + +( + +Boehme +et al. 1982 + +; +Khozatskiy 1985 +; + +Boehme +2010 + +; + +Rocek +et al. 2014 + +) allowed to suggest further diagnostic features for + +P. sanchizi + +such as: 1) the lateral superior process of the frontoparietal is longer than broad; 2) articulation surface on frontoparieals with squamosal well-developed, concave and oriented fully laterally. + + +The single premaxilla from Echzell shows a remarkable feature: ornamented on the anterior surface of the bone, recalling the pit-and-ridge sculpture of, e.g., frontoparietal and squamosal. Comparable ornamentation has not been ever described for the genus + +Pelobates + +and in + +P. sanchizi + +from other Miocene localities. Only for + +Eopelobates deani + +( + +Rocek +et al. 2014 + +), a moderated rugose outer surface has been mentioned. + + + + \ No newline at end of file diff --git a/data/38/E0/ED/38E0EDAE0834EA4EC4CAED7B81859157.xml b/data/38/E0/ED/38E0EDAE0834EA4EC4CAED7B81859157.xml new file mode 100644 index 00000000000..f01bbf9f79d --- /dev/null +++ b/data/38/E0/ED/38E0EDAE0834EA4EC4CAED7B81859157.xml @@ -0,0 +1,100 @@ + + + +Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea + + + +Author + +Dale-Skey, Natalie + + + +Author + +Askew, Richard R. + + + +Author + +Noyes, John S. + + + +Author + +Livermore, Laurence + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8013 +8013 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8013 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8013 +1314-2828-4-8013 + + + + +Ionympha ochus (Walker, 1839) + + + + +Entedon ochus +Walker, 1839 + + +natras +(Walker, 1839, +Cirrospilus +) + + +tegar +(Walker, 1839, +Entedon +) + + +vagellius +(Walker, 1839, +Entedon +) + + +antaradus +(Walker, 1848, +Entedon +) + + + +Distribution +England, Scotland + + + \ No newline at end of file diff --git a/data/38/E1/60/38E1607C091C3D00D417FBD92B10D222.xml b/data/38/E1/60/38E1607C091C3D00D417FBD92B10D222.xml new file mode 100644 index 00000000000..c996b4acd30 --- /dev/null +++ b/data/38/E1/60/38E1607C091C3D00D417FBD92B10D222.xml @@ -0,0 +1,63 @@ + + + +Discovery of Steninae from Ningxia, Northwest China (Coleoptera, Staphylinidae) + + + +Author + +Tang, Liang + + + +Author + +Li, Li-Zhen + +text + + +ZooKeys + + +2013 + +272 + + +1 +20 + + + + +http://dx.doi.org/10.3897/zookeys.272.4389 + +journal article +http://dx.doi.org/10.3897/zookeys.272.4389 +1313-2970-272-1 + + + + +Stenus deceptiosus Puthz, 2008 +Fig. 21 + + + + +Stenus deceptiosusi +Puthz, 2008b: 184. + + + +Material examined: +China: Ningxia: 7 ♂♂, 7 ♀♀, Jinyuan County, Qiuqianjia, 1800 m, 6.VII.2008, Wen-Xuan Bi leg.; 2 ♂♂, 3 ♀♀, Jingyuan County, Xixia, 15.VII. 2008, Feng Yuan leg. + + +Distribution. +China (Shaanxi, Shanxi, Ningxia, Hebei, Bejing, Liaoning), Korea. + + + \ No newline at end of file diff --git a/data/38/E1/9E/38E19EDB3683B889C5EE7AE641DC3FD1.xml b/data/38/E1/9E/38E19EDB3683B889C5EE7AE641DC3FD1.xml new file mode 100644 index 00000000000..0eb792f1242 --- /dev/null +++ b/data/38/E1/9E/38E19EDB3683B889C5EE7AE641DC3FD1.xml @@ -0,0 +1,179 @@ + + + +Flora der Schweiz und angrenzender Gebiete. Band 1. Pteridophyta bis Caryophyllaceae (2 nd edition): Registerzuband 1 + + + +Author + +Hess, Hans Ernst + + + +Author + +Landolt, Elias + + + +Author + +Hirzel, Rosmarie + +text + +1972 +Birkhaeuser Verlag + + +https://doi.org/10.5281/zenodo.291815 + +book +291815 +10.5281/zenodo.291815 +3-7643-0843-5 + + + +<subSubSection id="26978E1E49B5F42D4E52CFECCCA98E0C" pageId="null" pageNumber="107" type="nomenclature"> +<paragraph id="028C2C105E9741D9E5BA9FF592012740" pageId="null" pageNumber="107"> +<taxonomicName id="7B0A54D907DF6827671CB84AF613BD11" ID-CoL="63MZ9" authority="L." class="Polypodiopsida" family="Polypodiaceae" genus="Polypodium" kingdom="Plantae" order="Polypodiales" pageId="null" pageNumber="107" phylum="Tracheophyta" rank="genus"> +<pageBreakToken id="B1FAD67B63DC367BAC743D7B54C2637E" pageId="null" pageNumber="107" start="start"> +<normalizedToken id="F22C5BA5BE9B0E197615394EE7E7106F" originalValue="Polypódium" pageId="null" pageNumber="107">Polypodium</normalizedToken> +</pageBreakToken> +L. +</taxonomicName> +</paragraph> +</subSubSection> +<subSubSection id="40CA6DDA8F90D7B95920680BC65C7616" pageId="null" pageNumber="107" type="vernacular_names"> +<paragraph id="4260FF11C109DB26FE99E2ED523AF2F5" pageId="null" pageNumber="107"> +<normalizedToken id="F979F559AFBBE54528D042674A01C67C" originalValue="Tüpfelfarn" pageId="null" pageNumber="107">Tuepfelfarn</normalizedToken> +</paragraph> +</subSubSection> + + + +Farne von sehr verschiedenem Habitus (4-200cm hoch); +haeufig +epiphytisch; wenige Arten auf dem Boden lebend. Rhizom kriechend, meist dicht mit Spreuschuppen bedeckt. + +Blaetter +2zeilig und entfernt angeordnet + +oder +bueschelig +gedraengt +, +beim Absterben sich samt dem Stiel vom Rhizom abgliedernd +, ungeteilt, +handfoermig +geteilt, +fiederteilig +oder 1-4fach gefiedert, kahl oder mit Spreuschuppen oder Haaren, oft die sporentragenden +Blaetter +von den nicht sporentragenden verschieden. +Sori rund oder oval +(bei unsern Arten) bis +strichfoermig +, oft in Vertiefungen der Blattunterseite eingesenkt, sehr verschieden angeordnet (bei unsern Arten +in 2 Reihen auf jedem Abschnitt +). Ohne Schleier. + + +Die Gattung + +Polypodium +umfaβt +etwa 50 Arten, die vorwiegend im tropischen Asien und Amerika vorkommen; + +in Mitteleuropa lassen sich +vorlaeufig +3 nahe verwandte Arten unterscheiden (Manton 1950, Shivas 1961 1962, Lenski 1964); wie Peterken (1962) an einer Sippe aus England zeigt, kann die systematische Gliederung der Arten noch nicht abgeschlossen sein. + + +Verbreitungskarte unserer Artengruppe ( + +P. vulgare + +s. 1.) von Meusel (1964). + + + + + + + + + + + + + + + + + + + + +
+1. Zwischen den Sporangien (in den Sori) verzweigte, +druesige +, an Pilzhyphen erinnernde Gebilde (Paraphysen) vorhanden (50fache +Vergroesserung +, Paraphysen nicht mit Stielen von degenerierten Sporangien verwechseln; diese sind nie verzweigt!) + + +P + +. virginianum + + +(Nr. 1) +
1*. Keine Paraphysen zwischen den Sporangien.
+2. Blattspreite im +Umriss +oval bis 3eckig, 1,2-2,5-, selten bis 3mal so lang wie breit; Sori zum +grossen +Teil oval; Ring am Sporangium mit 4-8 kleinen Zellen mit stark verdickten, dunkelbraunen +Waenden +(100fache +Vergroesserung +) + + + +P. serratum + + +(Nr. 2) +
+2* Blattspreite im +Umriss +schmal lanzettlich, 4-5mal so lang wie breit; Sori rund; Ring am Sporangium mit 10-14 kleinen Zellen mit stark verdickten, dunkelbraunen +Waenden +(100fache +Vergroesserung +) + + + +P. vulgare + + +(Nr. 3) +
+
+ + + +<normalizedToken id="CEA93EF1DA3188904C4B11374B4CB529" originalValue="Schlüssel" pageId="null" pageNumber="107">Schluessel</normalizedToken> +zur Gattung +<taxonomicName id="4539AA9ECB60030274DD009EBEDA7D7F" class="Polypodiopsida" family="Polypodiaceae" genus="Polypodium" kingdom="Plantae" order="Polypodiales" pageId="null" pageNumber="107" phylum="Tracheophyta" rank="genus">Polypodium</taxonomicName> + + + +
+
+
\ No newline at end of file diff --git a/data/38/E2/04/38E204E80A1BF872F48347AC066EE963.xml b/data/38/E2/04/38E204E80A1BF872F48347AC066EE963.xml new file mode 100644 index 00000000000..4e76b2f4af1 --- /dev/null +++ b/data/38/E2/04/38E204E80A1BF872F48347AC066EE963.xml @@ -0,0 +1,56 @@ + + + +Nematodes from terrestrial and freshwater habitats in the Arctic + + + +Author + +Holovachov, Oleksandr + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1165 +1165 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1165 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1165 +1314-2828-2-1165 + + + + + +Eumonhystera similis ( +Buetschli +, 1873) + + + + +Notes + +Taymyr and Severnaya Zemlya, Russia ( +Gagarin 2001b +, +Kuzmin and Gagarin 1990 +). + + + + \ No newline at end of file diff --git a/data/38/E2/6C/38E26CA5C3F652A9BD5543CCD8D6D77E.xml b/data/38/E2/6C/38E26CA5C3F652A9BD5543CCD8D6D77E.xml new file mode 100644 index 00000000000..db45f371721 --- /dev/null +++ b/data/38/E2/6C/38E26CA5C3F652A9BD5543CCD8D6D77E.xml @@ -0,0 +1,235 @@ + + + +Integrative taxonomy and analysis of species richness patterns of nocturnal Darwin wasps of the genus Enicospilus Stephens (Hymenoptera, Ichneumonidae, Ophioninae) in Japan + + + +Author + +Shimizu, So +Laboratory of Insect Biodiversity and Ecosystem Science, Graduate School of Agricultural Science, Kobe University, Rokkodaicho 1 - 1, Nada, Kobe, Hyogo 657 - 8501, Japan & DC and Overseas Challenge Program for Young Researchers, Japan Society for the Promotion of Science, Tokyo, Japan & Depertment of Life Sciences, the Natural History Museum, Cromwell Road, London SW 7 5 BD, UK +https://orcid.org/0000-0002-5202-4552 +parasitoidwasp.sou@gmail.com + + + +Author + +Broad, Gavin R. +Depertment of Life Sciences, the Natural History Museum, Cromwell Road, London SW 7 5 BD, UK +https://orcid.org/0000-0001-7223-5333 + + + +Author + +Maeto, Kaoru +Laboratory of Insect Biodiversity and Ecosystem Science, Graduate School of Agricultural Science, Kobe University, Rokkodaicho 1 - 1, Nada, Kobe, Hyogo 657 - 8501, Japan + +text + + +ZooKeys + + +2020 + +990 + + +1 +144 + + + + +http://dx.doi.org/10.3897/zookeys.990.55542 + +journal article +http://dx.doi.org/10.3897/zookeys.990.55542 +1313-2970-990-1 +7B73642C278D40F89091B26213C9A704 +9F51F78CD53F5005A305DE65494002C4 + + + + +Enicospilus pseudopuncticulatus Shimizu +sp. nov. +Figure 35 + + + +Etymology. + +This species is very close to + +E. puncticulatus + +, hence the specific name based on their similarity. + + + +Type series. +Total of 8 specimens (5♀♀3♂♂): Japan (5♀♀3♂♂). + +HT: ♀, NIAES, Tsukuba City, Ibaraki Pref., +Kanto-Koshin +, JAPAN, 17-26.VII.1989, M. Sharkey leg. (NIAES). + + +PT: 1♂, Awashima, Niigata Pref., Hokuriku, JAPAN, 7.VII.1937, K. Baba & J. Sawano leg. (MNHA); 1♂, same data as HT (NIAES); 1♀, NIAES, Tsukuba City, Ibaraki Pref., +Kanto-Koshin +, JAPAN, 14-19.IV.1989, M. Sharkey leg. (EMUS); 2♀♀, Nokata, Nisshin, Aichi Pref., +Tokai +, JAPAN, 10-16.VII.2011 (1♀), 23-30.VII.2011 (1♀), H. Seo & R. Mizutani leg. (MsT) (ELMU); 1♀1♂, Niryou, Takatsuki City, +Ōsaka +Pref., Kinki, JAPAN, 30.VI-4.VIII.2013, S. Fujie leg. (MsT) (♀, MNHA, SEN176-DDBJ-LC492933; ♂, OMNH, SEN147-DDBJ-LC492932). + + + +Distribution. +Eastern Palaearctic region. + +JAPAN: [Hokuriku] Niigata; [ +Kanto-Koshin +] Ibaraki; [ +Tokai +] Aichi; [Kinki] +Ōsaka +. + + + +Bionomics. +Unknown. + + +Differential diagnosis. + +Although this species is very close to + +E. puncticulatus + +based on both morphology and DNA barcoding (Fig. +6 +), it is rather readily distinguishable by the linear central sclerite and straight fore wing vein 1cu-a, as in Fig. +35F +. + + + +Description. +Female (n = 5). Body length 20.0-22.0 (HT: ca. 20.5) mm. + +Head with GOI = 3.0-3.2 (HT: 3.1) (Fig. +35D +). Lower face 0.8 +x +as wide as high, strongly shiny, finely punctate with setae (Fig. +35B +). Clypeus 1.7-2.0 +x +(HT: 1.9) as wide as high, moderately punctate with setae as in upper face, moderately convex in profile, ventral margin impressed (Fig. +35B, D +). Malar space 0.3 +x +as long as basal mandibular width (Fig. +35B, D +). Mandible moderately twisted by 25-40° (HT: ca. 30°), rather long, proximally narrowed, distally parallel-sided, outer surface with diagonal setose groove (Fig. +35B, D +). Upper tooth of mandible 1.8-2.1 +x +(HT: 2.1) as long as lower (Fig. +35B +). Frons, vertex and gena strongly shiny with fine setae (Fig. +35B-D +). Posterior ocellus very close to eye (Fig. +35B-D +). Ventral end of occipital carina joining oral carina. Antennae with 66-69 (HT: 67) flagellomeres; first flagellomere 1.6-1.7 +x +(HT: 1.6) as long as second; 20th flagellomere 2.0-2.1 +x +(HT: 2.0) as long as wide. + + +Mesosoma entirely very strongly shiny with setae (Fig. +35E +). Pronotum diagonally striate to moderately punctate (Fig. +35E +). Mesoscutum 1.5 +x +as long as maximum width, finely punctate with setae, and evenly rounded in profile (Fig. +35E +). Notauli absent (Fig. +35E +). Scutellum moderately convex, finely punctate, with lateral longitudinal carinae along entire length of scutellum. Epicnemium densely punctate with setae. Epicnemial carina strong, evenly curved to anterior, dorsal end not reaching anterior margin of mesopleuron (Fig. +35E +). Mesopleuron entirely longitudinally striate to punctostriate (Fig. +35E +). Submetapleural carina broadened anteriorly (Fig. +35E +). Metapleuron entirely moderately punctate with diagonal striae posteriorly (Fig. +35E +). Propodeum declivous in profile; anterior transverse carina complete; anterior area longitudinally striate; spiracular area finely punctate with setae; posterior area finely to moderately rugose; propodeal spiracle elliptical and not joining pleural carina by ridge (Fig. +35E +). + + +Wings (Fig. +35F +). Fore wing length 13.0-14.0 (HT: ca. 13.0) mm with AI = 0.3-0.6 (HT: 0.5), CI = 0.2-0.3 (HT: 0.3), DI = 0.4, ICI = 0.5, SDI = 1.1-1.2 (HT: 1.1), SI = 0.2, SRI = 0.3; vein 1m-cu&M moderately sinuous; vein 2r&RS slightly sinuous; vein RS evenly curved; fenestra and sclerites of discosubmarginal cell as in Fig. +35F +; proximal sclerite rounded triangular, not confluent with distal sclerite, strongly pigmented; central sclerite linear and pigmented, subparallel to 2r&RS, positioned in medio-distal part of fenestra; distal sclerite moderately pigmented; proximal corner of marginal cell evenly setose; posterodistal corner of second discal cell 95-100° (HT: ca. 95°) and of subbasal cell 75-85° (HT: ca. 75°); vein 1cu-a antefurcal to M&RS by 0.1 +x +length of 1cu-a. Hind wing with NI = 1.3-1.4 (HT: 1.4); vein RS slightly evenly curved; vein RA with 7-8 (HT: 7) uniform hamuli. + + +Legs. Hind leg with coxa in profile 1.9-2.0 +x +(HT: 1.9) as long as deep; basitarsus 2.0-2.1 +x +(HT: 2.0) as long as second tarsomere; fourth tarsomere 4.5-4.6 +x +(HT: 4.6) as long as wide; tarsal claw simply pectinate. + + +Metasoma with DMI = 1.3-1.4 (HT: 1.3), PI = 2.9-3.3 (HT: 3.2), THI = 2.2-2.6 (HT: 2.3); thyridium suboval, moderately sized; ovipositor sheath not longer than posterior depth of metasoma (Fig. +35A +). + + +Colour (Fig. +35 +). Entirely red-brown except for apex of mandible black. Wings hyaline; sclerites pigmented and amber; veins red-brown. + +Male (n = 3). Very similar to female. + + +Figure 35. + +Enicospilus pseudopuncticulatus + +Shimizu, sp. nov. ♀ ( +A-E +HT +F +PT) +A +habitus +B +head, frontal view +C +head, dorsal view +D +head, lateral view +E +mesosoma, lateral view +F +central part of fore wing. + + + + + \ No newline at end of file diff --git a/data/38/E3/1F/38E31F63D7D0520CB97CAA6B09E367FE.xml b/data/38/E3/1F/38E31F63D7D0520CB97CAA6B09E367FE.xml new file mode 100644 index 00000000000..6a218e67ca3 --- /dev/null +++ b/data/38/E3/1F/38E31F63D7D0520CB97CAA6B09E367FE.xml @@ -0,0 +1,483 @@ + + + +Checklist of newly-vouchered annelid taxa from the Clarion-Clipperton Zone, central Pacific Ocean, based on morphology and genetic delimitation + + + +Author + +Wiklund, Helena +https://orcid.org/0000-0002-8252-3504 +Gothenburg Global Biodiversity Centre, Gothenburg, Sweden & Natural History Museum, London, United Kingdom & University of Gothenburg, Gothenburg, Sweden +helena.wiklund@marine.gu.se + + + +Author + +Rabone, Muriel +https://orcid.org/0000-0002-8351-2313 +Natural History Museum, London, United Kingdom + + + +Author + +Glover, Adrian G +https://orcid.org/0000-0002-9489-074X +Natural History Museum, London, United Kingdom +a.glover@nhm.ac.uk + + + +Author + +Bribiesca-Contreras, Guadalupe +https://orcid.org/0000-0001-8163-8724 +Natural History Museum, London, United Kingdom + + + +Author + +Drennan, Regan +https://orcid.org/0000-0003-0137-5464 +Natural History Museum, London, United Kingdom & University of Southampton, Southampton, United Kingdom + + + +Author + +Stewart, Eva C D +https://orcid.org/0000-0001-8383-5705 +Natural History Museum, London, United Kingdom & University of Southampton, Southampton, United Kingdom + + + +Author + +Boolukos, Corie M +Natural History Museum, London, United Kingdom + + + +Author + +King, Lucas D +Natural History Museum, London, United Kingdom + + + +Author + +Sherlock, Emma +Natural History Museum, London, United Kingdom + + + +Author + +Smith, Craig R +https://orcid.org/0000-0002-3976-0889 +University of Hawaii, Honolulu, United States of America + + + +Author + +Dahlgren, Thomas G +https://orcid.org/0000-0001-6854-2031 +NORCE Norwegian Research Centre, Bergen, Norway & University of Gothenburg, Gothenburg, Sweden & Gothenburg Global Biodiversity Centre, Gothenburg, Sweden + + + +Author + +Neal, Lenka +Natural History Museum, London, United Kingdom +l.nealova@nhm.ac.uk + +text + + +Biodiversity Data Journal + + +2023 + +2023-09-15 + + +11 + + +86921 +86921 + + + + +http://dx.doi.org/10.3897/BDJ.11.e86921 + +journal article +http://dx.doi.org/10.3897/BDJ.11.e86921 +1314-2828-11-e86921 +C611C2E2385050A296DFAE776F86CF82 + + + + +Chaetopteridae sp. (NHM_331) + + + +Materials + + +Type status: + +Other material +. +Occurrence: +catalogNumber: +NHMUK ANEA 2023.336 +; recordNumber: NHM_1163B; recordedBy: +Adrian Glover | Helena Wiklund | Thomas Dahlgren | Madeleine Brasier +; individualCount: +1 +; preparations: specimen stored in 80% non-denatured ethanol aqueous solution | DNA voucher stored in buffer; otherCatalogNumbers: 0174126615; associatedSequences: +OQ738564 +(COI); occurrenceID: +33907DBF-3CBE-5938-AFF9-D89E722F9420 +; +Taxon: +taxonConceptID: Chaetopteridae sp. (NHM_331); scientificName: Chaetopteridae; kingdom: Animalia; phylum: Annelida; class: Polychaeta; family: Chaetopteridae; taxonRank: family; scientificNameAuthorship: +Audouin +& +Milne Edwards +, 1833; +Location: +waterBody: Pacific; stateProvince: Clarion Clipperton Zone; locality: + +Ocean Mineral +Singapore +exploration claim +Stratum A + +; verbatimLocality: OMS +Stratum A +; maximumDepthInMeters: 4100; locationRemarks: +Deployment EB +05; at +Station S +2; from R/ +V Thomas G. Thompson Cruise +no. TN319; verbatimLatitude: 12'06.93; verbatimLongitude: 117'09.87; decimalLatitude: +12.1155 +; decimalLongitude: +-117.1645 +; geodeticDatum: WGS84; +Identification: +identifiedBy: +Helena Wiklund | Lenka Neal | Thomas Dahlgren | Adrian Glover | Madeleine Brasier | Regan Drennan | Eva Stewart +; dateIdentified: +2021-04-20 +; identificationRemarks: identified by DNA and morphology; +Event: +eventID: OMS1_AB02_EB05; samplingProtocol: +Brenke Epibenthic Sledge +; eventDate: +2015-02-26 +; eventTime: 21:29; habitat: Abyssal plain; fieldNotes: +Collected from epi net +(on the epibenthic sledge); +Record Level: +language: en; institutionCode: NHMUK; collectionCode: ZOO; datasetName: ABYSSLINE; basisOfRecord: PreservedSpecimen + +Type status: + +Other material +. + +Occurrence +: + +catalogNumber: +NHMUK ANEA 2023.335 +; recordNumber: NHM_0461; recordedBy: + +Adrian Glover +| +Helena Wiklund +| +Thomas Dahlgren +| +Magdalena Georgieva + +; individualCount: +1 +; preparations: specimen stored in 80% non-denatured ethanol aqueous solution | DNA voucher stored in buffer; otherCatalogNumbers: 0174127341; associatedSequences: +OQ746523 +(16S) | +OQ746839 +(18S) | +OQ738523 +(COI); occurrenceID: +3E51E30E-453C-5372-A61F-04D09B8071BD +; + +Taxon +: + +taxonConceptID: +Chaetopteridae +sp. (NHM_331); scientificName: +Chaetopteridae +; kingdom: +Animalia +; phylum: +Annelida +; class: +Polychaeta +; family: +Chaetopteridae +; taxonRank: family; scientificNameAuthorship: +Audouin +& +Milne Edwards +, 1833; + +Location +: + +waterBody: +Pacific +; stateProvince: +Clarion +Clipperton +Zone +; locality: + +UK +Seabed Resources Ltd +exploration area UK-1 +Stratum A + +; verbatimLocality: +UK +1 +Stratum A +; maximumDepthInMeters: 4160; locationRemarks: +Deployment BC +14; at +Station L +; from R/ +V Melville Cruise +no. MV1313; verbatimLatitude: 13°43.597; verbatimLongitude: 116°40.200; decimalLatitude: +13.72662 +; decimalLongitude: +-116.67 +; geodeticDatum: WGS84; + +Identification +: + +identifiedBy: + +Helena Wiklund +| +Lenka Neal +| +Thomas Dahlgren +| +Adrian Glover +| +Madeleine Brasier +| +Regan Drennan +| +Eva Stewart + +; dateIdentified: +2021-04-20 +; identificationRemarks: identified by DNA and morphology; + +Event +: + +eventID: +UK +1_AB01_BC14; samplingProtocol: + +USNEL +Box Core + +; eventDate: +2013-10-22 +; eventTime: 07:25; habitat: +Abyssal +plain; fieldNotes: Collected from +0-2 cm +layer of box core using a +300 micron +sieve; + +Record Level +: + +language: en; institutionCode: NHMUK; collectionCode: ZOO; datasetName: ABYSSLINE; basisOfRecord: + +PreservedSpecimen + +Type status: + +Other material +. + +Occurrence +: + +catalogNumber: +NHMUK ANEA 2023.334 +; recordNumber: NHM_0331; recordedBy: + +Adrian Glover +| +Helena Wiklund +| +Thomas Dahlgren +| +Magdalena Georgieva + +; individualCount: +1 +; preparations: specimen stored in 80% non-denatured ethanol aqueous solution | DNA voucher stored in buffer; otherCatalogNumbers: 0174127338; associatedSequences: +OQ746496 +(16S) | +OQ746815 +(18S); occurrenceID: +D3FE16FA-F760-5239-8DB1-BA9216776507 +; + +Taxon +: + +taxonConceptID: +Chaetopteridae +sp. (NHM_331); scientificName: +Chaetopteridae +; kingdom: +Animalia +; phylum: +Annelida +; class: +Polychaeta +; family: +Chaetopteridae +; taxonRank: family; scientificNameAuthorship: +Audouin +& +Milne Edwards +, 1833; + +Location +: + +waterBody: +Pacific +; stateProvince: +Clarion +Clipperton +Zone +; locality: + +UK +Seabed Resources Ltd +exploration area UK-1 +Stratum A + +; verbatimLocality: +UK +1 +Stratum A +; maximumDepthInMeters: 4075; locationRemarks: +Deployment RV +05; at +Station G +; from R/ +V Melville Cruise +no. MV1313; decimalLatitude: +13.76085 +; decimalLongitude: +-116.4653 +; geodeticDatum: WGS84; + +Identification +: + +identifiedBy: + +Helena Wiklund +| +Lenka Neal +| +Thomas Dahlgren +| +Adrian Glover +| +Madeleine Brasier +| +Regan Drennan +| +Eva Stewart + +; dateIdentified: +2021-04-20 +; identificationRemarks: identified by DNA and morphology; + +Event +: + +eventID: +UK +1_AB01_RV05; samplingProtocol: + +Remotely Operated Vehicle + +; eventDate: +2013-10-17 +; eventTime: 19:06; habitat: +Abyssal +plain; + +Record Level +: + +language: en; institutionCode: NHMUK; collectionCode: ZOO; datasetName: ABYSSLINE; basisOfRecord: +PreservedSpecimen + + + + + + + + + + +Distribution +Eastern Clarion-Clipperton Zone, central Pacific Ocean. + + +Diagnosis + +Damaged specimens (Fig. +15 +) consistent with placement within family +Chaetopteridae +, based on morphology and DNA. + + + + \ No newline at end of file diff --git a/data/38/E3/37/38E337CE6AB2C52047B786E067657533.xml b/data/38/E3/37/38E337CE6AB2C52047B786E067657533.xml new file mode 100644 index 00000000000..c7ba8d28e98 --- /dev/null +++ b/data/38/E3/37/38E337CE6AB2C52047B786E067657533.xml @@ -0,0 +1,53 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Perca argentea +[ +spec. nov. +] + + + + +P. pinnis dorsalibus unitis, cauda bifida, naribus tubulosis. +Mus. Ad. Fr. +2. +p +... @/D. {12/22}. P. 12. V. 1/6. A. {3/11}. C. 17. + + + + +Habitat +.. + + + + \ No newline at end of file diff --git a/data/38/E3/80/38E38030D4D88C18A70021760FE1B307.xml b/data/38/E3/80/38E38030D4D88C18A70021760FE1B307.xml new file mode 100644 index 00000000000..1310ac7adb7 --- /dev/null +++ b/data/38/E3/80/38E38030D4D88C18A70021760FE1B307.xml @@ -0,0 +1,97 @@ + + + +Checklist of British and Irish Hymenoptera - Sawflies, ' Symphyta' + + + +Author + +Liston, Andrew D. + + + +Author + +Knight, Guy T. + + + +Author + +Sheppard, David A. + + + +Author + +Broad, Gavin R. + + + +Author + +Livermore, Laurence + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1168 +1168 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1168 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1168 +1314-2828--1168 +3C3EC7B09BA145848E3E89CBBD28B432 +3C3EC7B09BA145848E3E89CBBD28B432 + + + + +Sirex juvencus (Linnaeus, 1758) + + + + +Ichneumon juvencus +Linnaeus, 1758 + + +Sirex nigricornis +Acerbi, 1802 + + +Sirex dubia +W. F. Kirby, 1882 + + + +Distribution +England, Scotland, Wales + + +Notes + +Sirex atricornis +is considered to be a valid species ( +Schiff et al. 2012 +), which may occur in Scotland ( +Viitasaari and Midtgaard 1989 +). + + + + \ No newline at end of file diff --git a/data/38/E3/9E/38E39EFC92905BD927F178A7039D40C8.xml b/data/38/E3/9E/38E39EFC92905BD927F178A7039D40C8.xml new file mode 100644 index 00000000000..d587390e4a0 --- /dev/null +++ b/data/38/E3/9E/38E39EFC92905BD927F178A7039D40C8.xml @@ -0,0 +1,122 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part C) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +370 +473 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Crotalaria lotifolia +Linnaeus + +, + +Species Plantarum +2 + +: 715. 1753 + + +, +typ. cons. + + + +"Habitat in Jamaica." RCN: 5258. + + + +Conserved type (Fawcett & Rendle, +Fl. Jamaica +4: 11. 1920): [icon] " + +Crotalaria trifolia +fruticosa foliis glabris, flore e viridi luteo minore + +" in Sloane, Voy. Jamaica 2: 33, t. 176, f. 1, 2. 1725. - + +Typotype +: Herb. Sloane 6: 5 ( +BM-SL +) + +. + + + + +Generitype +of + +Crotalaria +Linnaeus + +, +nom. cons. + + + + +Current name: + + +Crotalaria lotifolia + +L. + +( +Fabaceae +: +Faboideae +). + + + + + +Note: +Crotalaria lotifolia + +, with the type designated by Fawcett & Rendle, was proposed as conserved type of the genus by Jarvis (in +Taxon +41: 561. 1992). This was eventually approved by the General Committee (see review of the history of this proposal by Barrie, +l.c. +55: 795-796. 2006). + + + + \ No newline at end of file diff --git a/data/38/E4/1C/38E41C050597309DEE7FB2C034663576.xml b/data/38/E4/1C/38E41C050597309DEE7FB2C034663576.xml new file mode 100644 index 00000000000..9d9aa841db5 --- /dev/null +++ b/data/38/E4/1C/38E41C050597309DEE7FB2C034663576.xml @@ -0,0 +1,70 @@ + + + +Polychaetes of Greece: an updated and annotated checklist + + + +Author + +Faulwetter, Sarah + + + +Author + +Simboura, Nomiki + + + +Author + +Katsiaras, Nikolaos + + + +Author + +Chatzigeorgiou, Giorgos + + + +Author + +Arvanitidis, Christos + +text + + +Biodiversity Data Journal + + +2017 + +5 + + +20997 +20997 + + + + +http://dx.doi.org/10.3897/BDJ.5.e20997 + +journal article +http://dx.doi.org/10.3897/BDJ.5.e20997 +1314-2828--20997 + + + + +Syllis vittata Grube, 1840 + + + +Notes +Type locality: Mediterranean (Palermo, Sicily, Italy). + + + \ No newline at end of file diff --git a/data/38/E4/85/38E485C63936182A12FB6AD8BE2E0E9C.xml b/data/38/E4/85/38E485C63936182A12FB6AD8BE2E0E9C.xml new file mode 100644 index 00000000000..2bd5fd2a3fd --- /dev/null +++ b/data/38/E4/85/38E485C63936182A12FB6AD8BE2E0E9C.xml @@ -0,0 +1,76 @@ + + + +A biodiversity hotspot for Microgastrinae (Hymenoptera, Braconidae) in North America: annotated species checklist for Ottawa, Canada + + + +Author + +Fernandez-Triana, Jose + + + +Author + +Boudreault, Caroline + + + +Author + +Buffam, Joel + + + +Author + +Mclean, Ronald + +text + + +ZooKeys + + +2016 + +633 + + +1 +93 + + + + +http://dx.doi.org/10.3897/zookeys.63.10480 + +journal article +http://dx.doi.org/10.3897/zookeys.63.10480 +1313-2970-633-1 +DEFC153072414BA6B778CA63DB45B422 + + + +Taxon classification Animalia Hymenoptera Braconidae + + + +Microplitis jft21 + + + +Distribution. +NEA. + + +Notes. +This species corresponds in BOLD to BIN BOLD:AAE8603, with all specimens collected in eastern North America. + + +Material examined. +Ontario, Ottawa, city garden, 45.356 -75.707, 30.v.2007, H. Goulet, Voucher Code: CAM0228, CAM0231; 30.vii.2007, H. Goulet, Voucher Code: CAM0184. + + + \ No newline at end of file diff --git a/data/38/E4/9C/38E49C63B3175F48A9D861D444210704.xml b/data/38/E4/9C/38E49C63B3175F48A9D861D444210704.xml new file mode 100644 index 00000000000..be01b490feb --- /dev/null +++ b/data/38/E4/9C/38E49C63B3175F48A9D861D444210704.xml @@ -0,0 +1,120 @@ + + + +A new long-winged pygmy grasshopper in Eocene Baltic amber raises questions about the evolution of reduced tegmenula in Tetrigidae (Orthoptera) + + + +Author + +Skejo, Josip +https://orcid.org/0000-0002-2554-4499 +IUCN / SSC Grasshopper Specialist Group, Zagreb, Croatia. & SIGTET-Special Interest Group Tetrigidae, Karlsruhe, Germany. & University of Zagreb, Faculty of Science, Zagreb, Croatia. +skejo.josip@gmail.com + + + +Author + +Kasalo, Niko +https://orcid.org/0000-0002-3139-6349 +SIGTET-Special Interest Group Tetrigidae, Karlsruhe, Germany. & University of Zagreb, Faculty of Science, Zagreb, Croatia. +niko.kasalo5@gmail.com + + + +Author + +Thomas, M. Jared +https://orcid.org/0000-0002-4514-7757 +Center for Paleontology, Illinois Natural History & State Geological Surveys, Prairie Research Institute, University of Illinois at Urbana-Champaign, 1816 South Oak Street, Champaign, Illinois 61820, USA. + + + +Author + +Heads, Sam W. +Center for Paleontology, Illinois Natural History & State Geological Surveys, Prairie Research Institute, University of Illinois at Urbana-Champaign, 1816 South Oak Street, Champaign, Illinois 61820, USA. + +text + + +Journal of Orthoptera Research + + +2024 + +2024-01-09 + + +33 + + +1 + + +21 +26 + + + + +http://dx.doi.org/10.3897/jor.33.105144 + +journal article +http://dx.doi.org/10.3897/jor.33.105144 +1937-2426-1-21 +1A982C52DF7C42FEAD3B376A3380829E +F4AFA3B029D650488A8B76307DCFFD91 + + + + +Subfamily + +Batrachideinae +Bolivar +, 1887 + + + + + +Type genus. +- + + + +Batrachidea + +Serville, 1838. + + + + +Diagnosis. +- + +Antennae with more than 19 segments, paranota rectangular, mid-femora with sulcate dorsal margin, female spermatheca with two diverticula. + + + +Composition. +- + + +Batrachideini +(Southern and Northern America), +Cassitettigini +(Africa and SE Asia), +Bufonidini +(New Guinea, Australia, New Caledonia, and Solomon islands) ( +Storozhenko 2019 +), and +Rusmithini +trib. nov. +(Eocene Europe, extinct). + + + + \ No newline at end of file diff --git a/data/38/E6/93/38E6938B0F636517891EB84298055B81.xml b/data/38/E6/93/38E6938B0F636517891EB84298055B81.xml new file mode 100644 index 00000000000..b5ecfafc785 --- /dev/null +++ b/data/38/E6/93/38E6938B0F636517891EB84298055B81.xml @@ -0,0 +1,156 @@ + + + +Order Chiroptera - Family Vespertilionidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +451 +529 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Hypsugo anchietae +Seabra 1900 + + + + + + + +Hypsugo anchietae +Seabra 1900 + +, + +J. Sci. Math. Phys. Nat. +Lisboa +, ser. 2, 6: 26 + + +. + + + + +Type Locality: + +Angola +, Cahata. + + + + + +Vernacular Names: +Anchieta's Pipistrelle +. + + + + +Distribution: +Angola +, S Dem. Rep. +Congo +, +Zambia +, +Zimbabwe +, +KwaZulu-Natal +( +South Africa +). + + + + +Conservation: +IUCN +2003 and +IUCN +/ +SSC +Action Plan (2001) – Vulnerable as + +Pipistrellus anchietai + +. + + + + +Discussion: +The oldest name for this species may be + +bicolor + +, here listed as a synonym of + +Neoromicia tenuipinnis + +following +Hayman and Hill (1971) +; see discussion in +Koopman (1975) +and +Hill and Harrison (1987) +. Reviewed by +Cotterill (1996) +and +Kearney and Taylor (1997) +. Sometimes misspelled +anchieta +or + +anchietai + +, but the correct spelling is + +anchietae + +; see + +Kock (2001 +a +) + +. + + + + \ No newline at end of file diff --git a/data/38/E6/B9/38E6B99E01C141C314BD118112662017.xml b/data/38/E6/B9/38E6B99E01C141C314BD118112662017.xml new file mode 100644 index 00000000000..c19214fdfa3 --- /dev/null +++ b/data/38/E6/B9/38E6B99E01C141C314BD118112662017.xml @@ -0,0 +1,209 @@ + + + +First record of Rhopalophthalmuslongipes Ii, 1964 from Malaysian waters (Crustacea, Mysida) + + + +Author + +Tan, Hai Siang + + + +Author + +Azman, B. A. R. + +text + + +ZooKeys + + +2017 + +642 + + +53 +61 + + + + +http://dx.doi.org/10.3897/zookeys.642.10316 + +journal article +http://dx.doi.org/10.3897/zookeys.642.10316 +1313-2970-642-53 +D9E75D511FAB44A8B66A64C1598EA656 + + + + +Rhopalophthalmus longipes Ii, 1964 +Figs 2, 3, 4, 5 + + + + +Rhopalophthalmus longipes +Ii, 1964, 180, figs 46, 47; +Mauchline and Murano 1977 +, 75 [catalogue]; Muller 1993, 49 [catalogue]; +Wang and Liu 1994 +, 91, figs 14; +1997 +, 204; 2000, 114, figs 27; +Hanamura et al. 2011 +, 14, figs 8-10. + + + +Material examined. + +One immature female, 6.5 mm, UKMMZ-1553, Kampung Sebirah Kechil, Pulau Tinggi, Sultan Iskandar Marine Park, Johor, +02°18.581'N +, +104°05.624'E +, epibenthic sledge, 25th March 2012, 30.1 °C, depth 7 m, coll. Azman, B.A.R., Tan, H.S. and Shamsul, B.; eight immature females, six juveniles, UKMMZ-1554; three juveniles, UKMMZ-1555; two immature females, four juveniles, UKMMZ-1556; same station. Largest immature female, 6.9 mm, juveniles, 1.9-3.5 mm, males not collected. In the females, smaller than 5.9 mm, the pleopods are not fully developed. Juveniles: in the smallest specimens at our disposal, measuring 1.9 mm, the eyes are somewhat larger and with stouter stalk than in the adult. + + + +Description. +Based on immature female, 6.5 mm, UKMMZ-1553, Figs 2A, 5A. + + +Figure 2. +Rhopalophthalmus longipes +Ii, 1964, A immature female, 6.5 mm, UKMMZ-1553 B juvenile, 2.4 mm, UKMMZ-1554, Pulau Tinggi, Malaysia. + + + +Carapace short; anterior dorsal part of carapace between postorbital spines slightly produced, forming evenly rounded rostral plate; the postorbital spines sharp, supported by very short, feebly developed carina; antero-lateral angles of the carapace ( +"cheeks" +) somewhat sinuous or slightly concave; posterior dorsal margin excavate, leaving the last two to three posterior thoracic somites exposed completely in dorsal view; cervical sulcus well marked dorsally and laterally around anterior one-third, nodules not present on the dorsal surface of carapace, just posterior to cervical groove in addition to posterior one. + + +Eyes large and globular, somewhat shorter than the first joint of antennular peduncle; cornea well pigmented; the whole eye, including the stalk, nearly 1 +1/2 +times as long as broad, stalk nearly cylindrical, cornea occupying ⅓ of the eye and somewhat narrower than the distal end of the stalk (Fig. 3A). + + + +Figure 3. +Rhopalophthalmus longipes +; A anterior part of carapace B third segment of antennular peduncle C antennule D antenna and antenna scale E sympod spines of antenna F maxilla G maxillule. + + + +Antennular peduncle somewhat slender, first segment of antennular peduncle 1 ⅓ times as long as the combined length of distal two segments, armed with several setae along lateral margin; second segment shortest, slightly shorter than wide; third segment longer than wide, with three moderate setae, distal outer corner produced into a +triangular +process under the base of the outer flagellum and a rounded process bearing two protrusions (Fig. 3B) apically near the middle distal end (Fig. 3C). + +Antennal scale extending beyond the distal end of the antennular peduncle, approx. 6⅓-7 times as long as wide, the margins nearly parallel and equal width throughout; apex almost truncate; a distinct oblique suture marking off the small distal segment; disto-lateral spine slender, prominent and extending beyond the apex of the scale; sympod composed of four spines on the inner ventral face at the base of peduncle (Fig. 3E), two longer and two short spines, the most inner lateral spine around five times longer than the mesial one (Fig. 3D). +Labrum transverse, without process in front, mandibles with moveable lacinia thick, molar process thick, slightly produced, with teeth on the end, the palp moderately short, very feebly expanded. Maxilla (Fig. 3F) with the lobe from third segment deeply cleft, the palp elongated, the exopod rather small. + +Abdominal somites smooth, second to fifth somites nearly sub-equal in length, first and sixth somites 1 +1/2 +times as long as fifth one (Fig. 5A). + + +Endopods of pereopods (Figs 4A, B, C, D, E, F, 5B) slender and gradually increase in length posteriorly, remarkable in having proportionately long endopod particularly in seventh one; endopod of third to sixth pereopods similar in shape but length increasing posteriorly; endopod of third pereopod (Fig. 4C) slightly stouter than the +fourth +one, carpo-propodus divided into three articles, basal article sub-equal or slightly longer than the carpo-propodus; endopod of fourth to sixth pereopods (Figs 4D, 4E, 4F) having three-segmented carpo-propodus; endopod of seventh pereopod (Fig. 5B) longest, approx. +21/2 +times as long as the exopod, carpo-propodus divided into four articles, carpus noticeably long, as long as or longer than pereopod normally un-articulated, barely reaching mid-length of basal plate of exopod. + + + +Figure 4. +Rhopalophthalmus longipes +; A endopod of first pereopod B endopod of second pereopod C endopod of third pereopod D endopod of fourth pereopod E endopod of fifth pereopod F endopod of sixth pereopod. + + + + +Figure 5. +Rhopalophthalmus longipes +; A immature female (lateral view) B endopod of seventh pereopod C first pleopod D third pleopod E fifth pleopod F right uropod G telson. + + + +Pleopods +un-articulated, length generally increasing on posterior somites but that on third pleopod somewhat short, comparable to first one (Figs 5C, 5D, 5E). + + +Uropod two-segmented in both endopod and exopod; endopod sub-equal in length with telson, proximal segment with a strong stout seta at the middle of the ventral inner margin, distal segment +1/4 +of the endopod in length; exopod with outer margin very fine setose, somewhat longer than endopod with distal segment ⅖ of the exopod in length and +101/2 +times as long as wide (Fig. 5F). + + +Telson comparatively narrow and slender, 4 ⅖ times as long as basal wide, nearly same length as the sixth abdominal somite, extends distinctly beyond the articulations of the uropod, abruptly constricted beyond the articulations of the uropod but not forming discernible waist, and hardly broadens to first +1/2 +point with the lateral margins nearly parallel, in the next half gradually narrows distally with convex margins somewhat concave, and accordingly rather slightly broadens distally near the apex; distal half of the lateral margin armed with 7-9 strong spines, increasing in length posteriorly in the distal part but become again somewhat shorter towards the apex; apex narrowly rounded and armed with four extremely strong spines; the apical spines nearly equal in length with each other, ⅕ of the total length of the telson and furnished with secondary spinules, which are flattened like saw-teeth (Fig. 5G). + + + +Type locality. +Shizuoka, Japan + + +Distribution. + +Shizuoka, Nagasaki, Japan (Ii, 1964); Nansha Islands, the Spratlys (Wang and Liu, 1994); East China Sea (Wang and Liu, 1997); off Amami Island, south-western Japan; south-western part of South China Sea and western part of Timor Sea ( +Hanamura et al., 2011 +) and Pulau Tinggi, Johor, Malaysia (present study). + + + +Remarks. + +Rhopalophthalmus longipes +was first described by +Ii (1964) +based on the specimens collected from Japan. This species can be easily distinguished from others species in having a very narrow telson and secondary spinules on the apical spines of telson. Another distinct character within the genus is the endopod of third to seventh thoracopods gradually increasing in length posteriorly and the seventh endopod of thoracopod being more than twice as long as the exopod. + + +Rhopalophthalmus longipes +resembles +Rhopalophthalmus orientalis +, which was described by +Tattersall (1957) +from Japanese waters by having two long spines and two shorter spines at the antennal sympod and possessed peculiarly flattened teeth-saw like secondary spinules on the apical spines of telson. However, the seventh endopod of thoracopod in latter species is not as long as twice the length of exopod compared to +Rhopalophthalmus longipes +and the telson is conspicuously slender in the distal half compared to +Rhopalophthalmus orientalis +, which is moderately broad in distal half. In addition, +Rhopalophthalmus orientalis +has small triangular rostrum, which is not found in the +Rhopalophthalmus longipes +. +Rhopalophthalmus longipes +also shows resemblance to +Rhopalophthalmus terranatalis +O. Tattersall, 1957 collected from estuarine waters around the coasts of Natal from +Richard's +Bay (on the east to Langebaan Bay of the south-west coast), but seventh thoracic endopod of the latter species has seven sub-segments instead of four sub-segments with an unusually elongated carpus in +Rhopalophthalmus longipes +. + + +The specimens found in this study exhibit some slight differences from the +Rhopalophthalmus longipes +of +Hanamura et al. (2011) +as the small nodules near the cervical sulcus of the carapace were absent. The specimens at hand also differ from the speci +mens +described by +Ii (1964) +and +Hanamura et al. (2011) +by the combination of these characters; 1) presence of a triangular process under the base of the outer flagellum; 2) presence of a rounded process bearing two protrusions apically near the middle distal end of third segment of antennule peduncle; and 3) telson armed with only 7-8 moderately strong setae. + + + + \ No newline at end of file diff --git a/data/38/E7/17/38E71780D45F657DA29FC65F995D597A.xml b/data/38/E7/17/38E71780D45F657DA29FC65F995D597A.xml new file mode 100644 index 00000000000..d013988793e --- /dev/null +++ b/data/38/E7/17/38E71780D45F657DA29FC65F995D597A.xml @@ -0,0 +1,63 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Phalaena petiverella +[ +spec. nov. +] + + + + +P. +Tinea +alis subgriseis litura dorsali flava, apiceque punctis tribus nigris. + + + + +Habitat in +Svecia. + + + + +Magnitudo P. subcutanearum. Alae fusco-griseae +; +in +medio litura flava, quae unitur cum alae oppositae macula; +margo exterior intra apicem striatus, +& +apex +postice punctis tribus nigris notatus. + + + + \ No newline at end of file diff --git a/data/38/E7/30/38E7302D2CE0ED01506C77631F9CF170.xml b/data/38/E7/30/38E7302D2CE0ED01506C77631F9CF170.xml new file mode 100644 index 00000000000..a0e216f6640 --- /dev/null +++ b/data/38/E7/30/38E7302D2CE0ED01506C77631F9CF170.xml @@ -0,0 +1,82 @@ + + + +Macrobenthic fauna from an upwelling coastal area of Peru (Warm Temperate South-eastern Pacific province - Humboldtian ecoregion) + + + +Author + +Tasso, Vicente + + + +Author + +El Haddad, Mustapha + + + +Author + +Assadi, Carolina + + + +Author + +Canales, Remy + + + +Author + +Aguirre, Luis + + + +Author + +Velez-Zuazo, Ximena + +text + + +Biodiversity Data Journal + + +2018 + +6 + + +28937 +28937 + + + + +http://dx.doi.org/10.3897/BDJ.6.e28937 + +journal article +http://dx.doi.org/10.3897/BDJ.6.e28937 +1314-2828--28937 + + + + +Abarenicola affinis affinis (Ashworth, 1902) + + + + +Arenicola assimilis affinis +Ashworth, 1902 + + + +Notes +Types of substrate: soft bottom. Depth / bathymetric range: 0-15 m. Station code: BT1N(10, 12, 15); BT1S(12, 15); BT2N(0, 10, 12, 15); BT2S(12, 15); BT3N(15); BT3S(10, 15);BT4N(10, 15). + + + \ No newline at end of file diff --git a/data/38/E7/BE/38E7BE404E00A7C8F1660CCDFE97E0C5.xml b/data/38/E7/BE/38E7BE404E00A7C8F1660CCDFE97E0C5.xml new file mode 100644 index 00000000000..23e4c5e8ca6 --- /dev/null +++ b/data/38/E7/BE/38E7BE404E00A7C8F1660CCDFE97E0C5.xml @@ -0,0 +1,137 @@ + + + +Order Primates + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +111 +184 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Galago thomasi +Elliot 1907 + + + + + + + +Galago thomasi +Elliot 1907 + +, +Ann. Mag. Nat. Hist., ser. 7, 20: 189 + +. + + + + +Type Locality: + +Dem. Rep. +Congo +, Beni. + + + + + +Vernacular Names: +Thomas's Bushbaby +. + + + + +Distribution: +W +Uganda +and +Kivu district +of Dem. Rep. +Congo +. + + + + +Conservation: +CITES +– Appendix II; +IUCN +– Lower Risk (lc). + + + + +Discussion: + +G. demidoff + +species group. +Nash et al. (1989) +recognized + +G. thomasi + +as a full species, partially sympatric with + +demidoff + +; followed by + +Groves (2001 +c +) + +. Known only from specimens from W +Uganda +and +Kivu district +of Dem. Rep. +Congo +(including Idjwi Isl), but vocalizations ascribed to this species are recorded from all over the same range as + +G. demidoff + +. + + + + \ No newline at end of file diff --git a/data/38/E7/E7/38E7E7867F82358F9287DC1AFE71A7F8.xml b/data/38/E7/E7/38E7E7867F82358F9287DC1AFE71A7F8.xml new file mode 100644 index 00000000000..6041d1e3235 --- /dev/null +++ b/data/38/E7/E7/38E7E7867F82358F9287DC1AFE71A7F8.xml @@ -0,0 +1,104 @@ + + + +Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea + + + +Author + +Dale-Skey, Natalie + + + +Author + +Askew, Richard R. + + + +Author + +Noyes, John S. + + + +Author + +Livermore, Laurence + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8013 +8013 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8013 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8013 +1314-2828--8013 + + + + +Mesopolobus teliformis (Walker, 1834) + + + + +Platyterma teliforme +Walker, 1834 + + +cincticorne +(Walker, 1834, +Platyterma +) + + +terminale +(Walker, 1834, +Platyterma +) + + +placidus +( +Foerster +, 1841, +Pteromalus +) + + +brevicornis +(Thomson, 1878, +Eutelus +) + + +suavis +(Dalla Torre, 1898, +Pteromalus +) + + + + \ No newline at end of file diff --git a/data/38/E7/F1/38E7F1CEFA7E6B07BFB5FB46E3C52E55.xml b/data/38/E7/F1/38E7F1CEFA7E6B07BFB5FB46E3C52E55.xml new file mode 100644 index 00000000000..a1c59c6b8d5 --- /dev/null +++ b/data/38/E7/F1/38E7F1CEFA7E6B07BFB5FB46E3C52E55.xml @@ -0,0 +1,57 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828-4-9042 + + + + + +Microleptes aquisgranensis ( +Foerster +, 1871) + + + + + +Miomeris aquisgranensis +Foerster +, 1871 + + + +Distribution +England, Scotland, Wales + + + \ No newline at end of file diff --git a/data/38/E8/41/38E841A0FC520498A7D2B828D612453C.xml b/data/38/E8/41/38E841A0FC520498A7D2B828D612453C.xml new file mode 100644 index 00000000000..9750e8298f9 --- /dev/null +++ b/data/38/E8/41/38E841A0FC520498A7D2B828D612453C.xml @@ -0,0 +1,120 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part L) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +610 +650 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Leea aequata +Linnaeus + +, + +Systema Naturae +, ed. 12, 2 + +: 627; + +Mantissa Plantarum + +: 124. 1767 + + +, +typ. cons. + + + +"Habitat in India orientali. Kleynhoff." RCN: 7189. + + + + +Lectotype +(Ridsdale in +Blumea +22: 90. 1974): +Kleynhoff +, Herb. Linn. No. 1118.1 ( +LINN +) + +. + + + + +Generitype +of + +Leea +Linnaeus + +, +nom. cons. + + + + +Current name: + +Leea aequata +L. + +( +Leeaceae +). + + + + + +Note: +Leea Linnaeus + +, +nom. cons +, against + +Nalagu +Adans. + + + + + \ No newline at end of file diff --git a/data/38/E8/EC/38E8EC8867F8568DB8C17DCB75930E61.xml b/data/38/E8/EC/38E8EC8867F8568DB8C17DCB75930E61.xml new file mode 100644 index 00000000000..145d43fe3df --- /dev/null +++ b/data/38/E8/EC/38E8EC8867F8568DB8C17DCB75930E61.xml @@ -0,0 +1,1128 @@ + + + +Identification of the rare deep-dwelling goby Suruga fundicola Jordan & Snyder, 1901 (Gobiiformes, Gobiidae) from the Yellow Sea + + + +Author + +An, Changting +National Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, 106 Nanjing Road, Qingdao, Shandong, China & Laboratory for Marine Fisheries Science and Food Production Processes, Laoshan Laboratory, Qingdao, China + + + +Author + +Li, Ang +National Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, 106 Nanjing Road, Qingdao, Shandong, China & Laboratory for Marine Fisheries Science and Food Production Processes, Laoshan Laboratory, Qingdao, China + + + +Author + +Wang, Huan +National Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, 106 Nanjing Road, Qingdao, Shandong, China & Laboratory for Marine Fisheries Science and Food Production Processes, Laoshan Laboratory, Qingdao, China + + + +Author + +Li, Busu +National Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, 106 Nanjing Road, Qingdao, Shandong, China & Laboratory for Marine Fisheries Science and Food Production Processes, Laoshan Laboratory, Qingdao, China + + + +Author + +Liu, Kaiying +National Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, 106 Nanjing Road, Qingdao, Shandong, China + + + +Author + +Sun, Hongyue +National Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, 106 Nanjing Road, Qingdao, Shandong, China + + + +Author + +Liu, Shufang +National Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, 106 Nanjing Road, Qingdao, Shandong, China & Laboratory for Marine Fisheries Science and Food Production Processes, Laoshan Laboratory, Qingdao, China +liusf@ysfri.ac.cn + + + +Author + +Zhuang, Zhimeng +National Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, 106 Nanjing Road, Qingdao, Shandong, China + + + +Author + +van der Laan, Richard +Grasmeent 80, 1357 JJ Almere, Netherlands + +text + + +Zoosystematics and Evolution + + +2023 + +2023-10-05 + + +99 + + +2 + + +489 +501 + + + + +http://dx.doi.org/10.3897/zse.99.102345 + +journal article +http://dx.doi.org/10.3897/zse.99.102345 +1860-0743-2-489 +BED03B874DB04940BC16A1886CC92EF7 +EFD119AD931D5A2C98E3D9C5BCC98972 + + + + +Suruga fundicola Jordan & Snyder, 1901 + + + + +Figs 2 +, 3 + + + + +Suruga fundicola +Jordan & Snyder, 1901: 96, fig. 20 (original description, type locality: Sagami Sea, Japan); +Akihito et al. 1984 +: 279 (in English), fig. 253-H; Akihito et al. 2002: 1207 (in Japanese); +Akihito et al. 2013 +: 58 (in Japanese); +Shibukawa and Iwata 2013 +a: 45; Matsui et al. 2014: 6; +Choi and Lee 2019 +:255, fig. 1. + + + +Diagnosis. + +Distinct from all other gobies ( +Gobiidae +), members of the + +Acanthogobius + +-group share a unique dominant pattern of the dorsal-pterygiophore formula, 3/I II II I I I 0 ( +Akihito et al. 1984 +). In the + +Acanthogobius + +-group, + +S. fundicola + +can be distinguished from the species of + +Sagamia + +, + +Siphonogobius + +and + +Pterogobius + +by possessing no free rays in the upper part of the pectoral fin and the posterior margin of the pelvic frenum indented. + +S. fundicola + +can be distinguished from the species of + +Lophiogobius + +, + +Amblychaeturichthys + +, and + +Chaeturichthys + +by the lack of barbels or flaps on the ventral surface of the head (except for the mental frenum). From species of + +Acanthogobius + +, + +S. fundicola + +can be distinguished by the large eye, its diameter greater than the snout length (vs. usually less); each cephalic sensory papilla formed into a minute skin flap (vs. not), the posterior oculoscapular canal absent (vs. posterior oculoscapular canal and its terminal pores +K' +and +L' +present). + + + +Description of Yellow Sea specimens. + +The counts and measurements are given in Table +1 +. Dorsal-fin rays VIII-I, 16; anal-fin rays I, 15 (1), I, 16 (3); pectoral-fin rays 20 (3), 21 (1); pelvic fin rays I, 5 (4); longitudinal scales 39 (1), 40 (2), 41 (1); pre-dorsal mid-line scales 10 (1), 11 (3); transverse scales 8 (1), 9 (2); 10 (1); vertebral count 14+21 = 35 (4); dorsal-pterygiophore formula 3/I II II I I I 0 i/12; epural 2; anal-fin pterygiophores anterior to first haemal spine 2. + +The following measurements are in % SL: head length 24.5-28.0 (mean 26.1); head depth 13.1-17.6 (15.4); head width 13.2-14.2 (13.6); snout length 4.5-5.7 (5.5); eye diameter 8.1-9.7 (8.7); interorbital width 0.9-1.9 (1.4); jaw length 8.3-10.3 (9.0); body width 10.6-10.3 (11.8); body depth at origin of first dorsal fin 15.3-22.4 (18.9); body depth at origin of anal fin 16.0-18.3 (16.9); snout to origin of first dorsal fin 31.5 -33.4 (32.5); snout to origin of second dorsal fin 53.3-58.7 (55.1); snout to origin of anal fin 55.7-61.1 (59.1); caudal peduncle length 10.7-13.5 (11.7); caudal peduncle depth 6.9-8.8 (8.0); pectoral fin length 19.5-21.8 (20.6); base of dorsal fin 13.8-14.7 (14.3); base of second dorsal fin 33.7-36.6 (35.4); base of anal fin 30.2-37.7 (32.4); caudal fin length 19.8-23.3 (21.4). + +General body appearance was shown in Figs +2 +, +3 +. Body small, moderately elongated; predorsal body profile slightly convex; ventral profile slightly concave, especially from pectoral-fin insertion to anal-fin origin. Head large, not depressed, short but longer than wide, depth and width less than those of the body. Snout short, obtuse in lateral and dorsal view, shorter than eye diameter and postorbital head length. Eyes notably large, situated dorsolateral in upper half of the head, with very narrow interorbital space, eyes nearly meeting, diameter larger than interorbital space or snout length. Mouth almost terminal, but upper jaw slightly protruding. Maxillary concealed except at its posterior end. Tongue thick, rather broad, round anteriorly. Gill openings broad, extending anteriorly to the vertical line of the posterior margin of the eye; upper edge of the gill opening on fleshy pectoral-fin base, slightly above the upper margin. No barbels. Body covered with cycloid scales, anterior small, posterior large and the scales are rather loosely attached. Head naked. + + + +Figure 3. +Lateral ( +a +), dorsal ( +b +), and ventral ( +c +) views of + +S. fundicola + +: YSFRI27216, 63.5 mm SL. + + +Fins flexible, without spinous rays. First dorsal fin with 8 slender spines, reaching origin of second dorsal when depressed; dorsal-pterygiophore formula 3/I II II I I I 0 i/12. Second dorsal fin with 1 simple and 16 branched rays, shorter than the first spines. Origin of first dorsal fin posterior to a vertical through base of pectoral fins, first dorsal fin without filamentous spines. The distal margin of the first dorsal fin is convex, when adpressed, the distal tip touches the base of the spine of the second dorsal fin. Dorsal fins discontinuous. Origin of second dorsal fin somewhat at vertical through the anus, and anterior to the anal fin. When adpressed, the distal tips of the second dorsal fin and the anal fins do not reach the procurrent rays of the caudal fin. Pectoral fins rounded, with 20 rays. The pectoral fin extends posteriorly to the vertical line through the posterior margin of the base of the first dorsal fin. Pelvic fin fused into a disc, each with 1 simple and 5 branched rays. Anal fin with 15-16 rays, the anterior of the anal fin below the third branched dorsal ray of the second dorsal fin. Segmented caudal-fin rays 7+7, upper unsegmented caudal fin rays about 12 and lower unsegmented caudal fin rays about 11. + +Cephalic canals are variably developed and are shown in Fig. +4 +: anterior oculoscapular canal (AOC) with B′, D (S), F, +H' +; posterior oculoscapular canal (POC) absent; preopercular canal (PC) with pores M′ and +O' +; four short longitudinal sensory papillae (SSP) rows (=rows r, u, s, t) on snout; four SSP rows (=rows g, j, k, and l) close behind the eye; two SSP rows (=rows h, i) before dorsal fin; two transverse sensory papillae (TSP) rows (=rows n and o) on snout and behind the eye, respectively; four longitudinal sensory papillae (LSP) rows (=rows a, b, c, and d) on the cheek; anterior end of row a approaches the anterior margin of the eye; rows b and c very close together; row cp with a single sensory papilla; row d arc-shaped, extending posteriorly to the vertical line through the posterior margin of the pupil; two long parallel longitudinal rows of sensory papillae just behind the chin (=row f), and ending on both sides at the opercles, one TSP row (=row ot) and two LSP rows (=rows os and oi) on the opercles, row ot extends to the ventral side. + + + +Figure 4. +Dorsal (top), lateral (middle), and ventral (bottom) views of the head of + +S. fundicola + +: YSFRI27216, 63.5 mm SL female), showing cephalic sensory canal pores (indicated by roman uppercase letters, except for AN and PN) and papillae (indicated by roman lowercase letters). AN and PN, indicated anterior and posterior nares, respectively. + + + +Cranium flat, frontals extremely narrow (Fig. +5a, e +). No suborbital bone. Five branchiostegal rays, the first one thin, and last one strong (Fig. +5f +). Four pairs of ceratobranchials (Fig. +5g +). Well-developed teeth on upper and lower pharyngeal. Three pairs of otoliths, sagittae, lapillus and asteriscus (Fig. +5e +). Vertebral count 35, 14 abdominal vertebrae (av) and 21 caudal vertebrae (cv), 14 pairs of ribs appending on parapophysis (Fig. +5a, b +). Three hypurals (HY), respectively HY1+2 (HY1 and HY2 fused into one), HY3+4 (HY3 and HY4 fused into one), and HY5; two epurals, EP1 and EP2. + + + +Figure 5. +Micro-CT images of right ( +a +), dorsal ( +b +), and ventral ( +c +) views of specimen YSFRI27216; front ( +d +) dorsal ( +e +), ventral ( +f +), and oblique view ( +g +) of the head of specimen YSFRI27216. 1. teeth, 2. premaxilla, 3. maxilla, 4. palatine, 5. ectethmoid, 6. parasphenoid, 7. frontal, 8. parietal, 9. supraoccipital, 10. neural spine, 11. first dorsal fin spines, 12. interdorsal pterygiophores, 13. pterygiophore, 14. second dorsal fin rays, 15. neural spine of preural centrum 3(NPU3), 16. neural spine of preural centrum 2(NPU2), 17. epural 1 (EP1), 18. epural 2 (EP2), 19. urostyle, 20. hypural 5 (HY5), 21. hypural 3+4 (HY3+4), 22. hypural 1+2 (HY1+2), 23. dental, 24. articular, 25. sympletic, 26. branchiostegal rays, 27. preopercular, 28. subopercular, 29. proximal radials, 30. pectoral fin soft rays, 31. pelvic fin spine, 32. vertebral canal, 33. boundary of abdominal vertebra and candal vertebrae, 34. anal fin rays, 35. ventrispinales, 36. haemal spine of preural centrum 3 (HPU 3), 37. haemal spine of preural centrum 2 (HPU 2), 38. parhypural (PH), 39. caudal fin ray, 40. rib, 41. parapophysis, 42. pelvic bone, 43. ethmoid, 44. lapillus 3+4 (HY3+4), 45. sagittae, 46. asteriscus, 47. basihyal, 48. ceratohyal, 3 (HPU 3). 49. epihyal, 50. cleithrum, 51. pharyngeal tooth, 52. ceratobranchial. + + + + +Coloration. + +In freshly collected specimens (Fig. +2 +), head and dorsum of body dusky, darker on snout, with several irregular light-yellow blotches on the lateral body, ventral body lighter, abdomen almost white. Pupil of the eye black, iris golden gray. A light sapphirine blotch present on the gill cover. Six or seven large dark spots scattered along middle of the side from the gill opening to the caudal-fin base; 2 or 3 light orange stripes on gray dorsal and caudal fins, the anterior margin of first dorsal fin with dusky spots, the upper posterior of caudal fin with a black stripe, anal fin somewhat gray. + +Coloration changed after 2 months of preservation (10% formalin preservative and then transformed to 75% alcohol), the yellow and orange pigment disappeared from body and fins, and the body of the fish became dark-yellowish, covered with tiny black spots, back darker and belly lighter, snout black, lateral dark spots not clear. Pupil of the eye white, iris golden black. Dorsal, pectoral, pelvic and anal fins light greyish. + + +Distribution. + +Northwest Pacific: off Pacific coasts from Miyagi Prefecture to Tosa Bay, Japan Sea from Aomori to Yamaguchi Prefecture, Okinawa Trough ( +Akihito et al. 2013 +), Southern Sea of Korea ( +Choi and Lee 2019 +), East China Sea ( +Okiyama 2014 +) and Yellow Sea (present study). + + + +Habitat and ecology. + +The four specimens were collected at depths between 69 and 74 meters (Fig. +1 +). The two stations maintained a relatively low temperature of about 10 °C and a high salinity of about 33‰ in April and July 2022 (Table +3 +). This species is considered as one of the deepest dwelling goby in Japan, known from depths of 40 to 400 meters ( +Akihito et al. 2013 +; +Choi and Lee 2019 +). + + +The catch at the stations mainly consists of ophiuroids, molluscs, jellyfishes, fishes and so on, most common species of which are the brittle stars + +Ophiura sarsii vadicola + +Djakonov, 1954 ( +Ophiuroidea +) and + +Stegophiura sladeni + +(Duncan, 1879) ( +Ophiuroidea +) (Fig. +6 +). Examples of the co-existing fish species are + +Jaydia lineata + +(Temminck & Schlegel, 1843) ( +Apogonidae +), + +Cleisthenes pinetorum + +Jordan & Starks, 1904 ( +Pleuronectidae +), + +Liparis tanakae + +(Gilbert & Burke, 1912) ( +Liparidae +), + +Pholis fangi + +(Wang & Wang, 1935) ( +Pholidae +), and + +Hexagrammos otakii + +Jordan & Starks, 1895 ( +Hexagrammidae +). + + + +Figure 6. +The catch of A: H27 (15 April), B: H12 (15 July), and C: H27 (20 July). + + + +Sequence characteristics and phylogenetic placement. The concatenated +COI +and +12S +sequences from 22 species were 704 bp in length (after trimming, except LC069781), including 400 conserved sites, 307 variable sites, 278 parsimony informative sites, and 24 singleton sites. The mean four nucleotide frequency of + +S. fundicola + +was A=26.1%, T=28.8%, C=27.3% and G =17.8%, slightly A-T rich (54.9%). The intragroup sequence divergence of + +S. fundicola + +was 0.5%; the genetic distance between samples of the Yellow Sea and the sequence (LC069781) of + +S. fundicola + +from west of Jogashima Island of Japan was 0.2%. This species has a genetic distance of 19.2% ( + +C. stigmatias + +) to 26.3% ( + +E. newberryi + +) to the other 20 species we used (see Table +4 +). The ML tree based on the concatenated sequences is shown in Fig. +7 +. In the tree topology, all species from the same genus clustered in one lineage; the four sequences of + +S. fundicola + +clustered into a highly supported (94% bootstrap P value) lineage and had a sister group relationship with the lineage formed by + +A. hexanema + +and + +C. stigmatias + +. + + + +Figure 7. +ML tree inferred from concatenated +COI +and +12S +sequences. Numbers at major internal nodes are bootstrap probability values. Sequences with * were sequenced in the present study. + + + + +Table 4. +Genetic distances (%) based on concatenated +COI +and +12S +sequences computed by MEGA X among 21 groups. + +S. fundicola + +* was sequenced for the present study. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
-GroupIntragroupIntergroup
1234567891011121314151617181920
1. + +Suruga fundicola + +* +0.5--------------------
2. + +S. fundicola + +n/c0.2-------------------
3. + +Am. hexanema + +0.521.519.5------------------
4 + +Ac. flavimanus + +n/c23.926.526.6-----------------
5 + +Ac. hasta + +n/c24.422.923.713.6----------------
6 + +C. stigmatias + +n/c19.217.915.125.622.8---------------
7 + +Lo. ocellicauda + +n/c21.620.127.321.220.925.5--------------
8 + +Ch. gulosus + +n/c23.514.826.624.625.223.420.2-------------
9 + +Ch. annularis + +n/c23.916.125.726.325.325.025.311.2------------
10 + +Gy. urotaenia + +n/c21.418.725.024.322.623.723.615.215.4-----------
11 + +Gy. petschiliensis + +n/c23.522.225.926.023.825.324.016.916.22.8----------
12 + +P. polynema + +n/c24.021.827.922.926.126.321.327.028.523.923.1---------
13 + +E. newberryi + +n/c26.322.631.425.024.528.226.819.721.621.021.826.9--------
14 + +Gi. mirabilis + +n/c20.912.623.924.721.423.320.617.421.417.118.723.420.1-------
15 + +Le. lepidus + +n/c21.116.124.924.122.922.024.319.220.216.016.924.717.216.2------
16 + +Lu. platycephalus + +n/c21.415.524.523.223.823.622.213.714.014.114.823.319.315.617.5-----
17 + +Lu. pallidus + +n/c22.820.222.823.522.321.224.215.415.413.114.024.619.315.916.510.9----
18 + +T. bifasciatus + +n/c25.029.026.226.325.424.724.524.425.123.223.525.024.424.725.325.124.6---
19 + +T. trigonocephalus + +n/c23.729.026.225.425.826.926.827.526.124.824.824.328.024.625.524.024.812.9--
20 + +R. similis + +n/c20.114.823.023.824.022.223.319.421.418.719.722.222.918.619.218.320.021.121.9-
21 + +O. haifengensis + +n/c22.523.527.124.126.226.324.525.726.422.421.824.124.824.422.822.720.929.727.322.3
+
+
+ +Material examined. + + +YSFRI27216-27217, +2 specimens +, +51.2-63.5 mm +SL, station H27, +Yellow Sea +, off +Qingdao +, +Shandong Province +, +China +( +35°59.69'N +, +123°07.63'E +), collected by +Changting An +on 15 April, 2022; YSFRI36942, +1 specimen +, +60.5 mm +SL, station H12, Yellow Sea, off Lianyungang, +Jiangsu Province +, +China +( +33°59.88'N +, +123°24.14'E +), collected by +Hongyue Sun +, on 16 July, 2022; YSFRI36943, +1 specimen +, +59.1 mm +SL, station H27, Yellow Sea, off Qingdao, +Shandong Province +, +China +( +35°56.03'N +123°07.54'E +), collected by +Hongyue Sun +, on 20 +July +, 2022 + +. + + +
+
\ No newline at end of file diff --git a/data/38/E9/76/38E9769E81EC2EC54E5BCE6490AA45EC.xml b/data/38/E9/76/38E9769E81EC2EC54E5BCE6490AA45EC.xml new file mode 100644 index 00000000000..64a3a4e891f --- /dev/null +++ b/data/38/E9/76/38E9769E81EC2EC54E5BCE6490AA45EC.xml @@ -0,0 +1,129 @@ + + + +Revision of the genus Pseudapanteles (Hymenoptera, Braconidae, Microgastrinae), with emphasis on the species in Area de Conservacion Guanacaste, northwestern Costa Rica + + + +Author + +Fernandez-Triana, Jose L. + + + +Author + +Janzen, Daniel H. + + + +Author + +Hallwachs, Winnie + + + +Author + +Whitfield, James B. + + + +Author + +Smith, M. Alex + + + +Author + +Kula, Robert + +text + + +ZooKeys + + +2014 + +446 + + +1 +82 + + + + +http://dx.doi.org/10.3897/zookeys.446.8195 + +journal article +http://dx.doi.org/10.3897/zookeys.446.8195 +1313-2970-446-1 +6EECF6D3C26B4844B6E13E72695297F7 +6EECF6D3C26B4844B6E13E72695297F7 + + + +Taxon classification Animalia Hymenoptera Braconidae + + + + +Pseudapanteles jorgerodriguezi +Fernandez-Triana +& Whitfield + +sp. n. +Figs 65- 69 + + + + +Holotype +. + +♀ in CNC. COSTA RICA, ACG, Alajuela Province, Sector San Cristobal, Estacion San Gerardo, 575m, 10.88009, -85.38887, 22.vii.2007. ACG database code: DHJPAR0025854. + + +Diagnosis. + +It belongs to the +annulicornis +species-group, and can be separated from other species within that group based on the combination of ovipositor sheaths length, T2 mostly longitudinally striate (except for small smooth central area), propodeum mostly smooth (with only median longitudinal carina), and scutoscutellar sulcus with 6 impressed pits. + + + +Description. + +Female. Body length 2.0-2.1 mm. Fore wing length 2.2-2.3 mm. Head color: mostly dark brown to black, except for yellow clypeus, labrum, mandibles, and spot on lower corner of gena near oral foramen. Flagellomere color: all flagellomere brown to black. Mesosoma color: entirely dark brown to black. Metasoma color (dorsally): mostly dark brown to black, except for yellow-orange anterior 0.4-0.6 of mediotergite 1. Coxae color: pale/pale/mostly or completely dark. Metatibia color: mostly pale, with posterior 0.1-0.2 dark. Metatarsus color: dark. Pterostigma color: entirely dark. Mediotergite 1 length/width at posterior margin 4.1-4.5 +x +. Mediotergite 1 maximum width/width at posterior margin 2.1-2.2 +x +. Mediotergite 2 width at posterior margin/length: 4.0-4.1 +x +. Mediotergite 2 sculpture: Mostly with longitudinally striate sculpture (sometimes with small, smooth area centrally). Ovipositor sheaths length: 0.9 +x +as long as metatibia. + +Male. Unknown. + + +Molecular data. +Sequences in BOLD: 1, barcode compliant sequences: 1. + + +Biology/ecology. +Malaise-trapped. + + +Distribution. +Costa Rica, ACG rain forest. + + +Etymology. +This species is named in honour of Sr. Jorge Rodriguez, who as a forester and a Costa Rican Vice-Minister and Minister of the Environment helped ACG forge new paths of self-support through Environmental Service Payments (Pagos para Servicios Ambientales). + + + \ No newline at end of file diff --git a/data/38/EA/3A/38EA3AEE3B8DD54D0180738B7D455776.xml b/data/38/EA/3A/38EA3AEE3B8DD54D0180738B7D455776.xml new file mode 100644 index 00000000000..369f803474e --- /dev/null +++ b/data/38/EA/3A/38EA3AEE3B8DD54D0180738B7D455776.xml @@ -0,0 +1,171 @@ + + + +Info Flora Schweiz - Caryophyllaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/caryophyllaceae.html + +url + + + + + +Minuartia mediterranea +(Link) K. +Maly + + + + + +Art ISFS: 261280 Checklist: 1029160 +Caryophyllaceae +Minuartia + +Minuartia mediterranea (Link) K. +Maly + + + +Zusammenfassung +KEINE ANGABE + + + +Oekologie + + + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + +KEINE ANGABE + + +
+
+
+
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F--Lichtzahl L--Salzzeichen--
Reaktionszahl R--Temperaturzahl T--
+Naehrstoffzahl +N +-- +Kontinentalitaetszahl +K +--
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Minuartia mediterranea +(Link) K. +Maly + + + + + +Volksname + + + +Deutscher Name: -- Nom +francais +: -- Nome italiano: -- + + + + +Status Indigenat +: Neophyt: nach der Entdeckung von Amerika in der Region aufgetreten (nach 1500) + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein + + +
+
\ No newline at end of file diff --git a/data/38/EA/71/38EA71E19843FC15B74077B756012EC3.xml b/data/38/EA/71/38EA71E19843FC15B74077B756012EC3.xml new file mode 100644 index 00000000000..233bc7fffce --- /dev/null +++ b/data/38/EA/71/38EA71E19843FC15B74077B756012EC3.xml @@ -0,0 +1,1227 @@ + + + +The Giant Resin Bee, Megachilesculpturalis Smith: New Distributional Records for the Mid- and Gulf-south USA + + + +Author + +Parys, Katherine A. + + + +Author + +Tripodi, Amber D. + + + +Author + +Sampson, Blair J. + +text + + +Biodiversity Data Journal + + +2015 + +3 + + +6733 +6733 + + + + +http://dx.doi.org/10.3897/BDJ.3.e6733 + +journal article +http://dx.doi.org/10.3897/BDJ.3.e6733 +1314-2828-3-6733 + + + + +Megachile (Callomegachile) sculpturalis Smith, 1853 + + + +Materials + + +Type status: +Other material +. Occurrence: recordedBy: +Amber D. Tripodi +; individualCount: +1 +; sex: +male +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Arkansas; county: Benton; municipality: Gentry; locality: +Chesney Prairie +; decimalLatitude: +36.221636 +; decimalLongitude: +-94.484357 +; Identification: identifiedBy: Amber D. Tripodi; Event: year: 2012; month: 6; day: 20; verbatimEventDate: +20-6-2012 +; Record Level: type: PhysicalObject; language: en; institutionCode: +BBSL +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Amber D. Tripodi +; individualCount: +1 +; sex: +male +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Arkansas; county: Benton; municipality: Rogers; locality: +Searles Prairie +; decimalLatitude: +36.356395 +; decimalLongitude: +-94.144186 +; Identification: identifiedBy: Amber D. Tripodi; Event: year: 2012; month: 6; day: 20; verbatimEventDate: +20-6-2012 +; Record Level: type: PhysicalObject; language: en; institutionCode: +BBSL +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Amber D. Tripodi +; individualCount: +1 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Arkansas; county: Madison; municipality: Hindsville; decimalLatitude: +36.206389 +; decimalLongitude: +-93.850278 +; Identification: identifiedBy: Amber D. Tripodi; Event: samplingProtocol: +Xylocopa virginica trap +; year: 2012; month: 6; day: 19; verbatimEventDate: +19-6-2012 +; Record Level: type: PhysicalObject; language: en; institutionCode: +BBSL +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +T. D. Edwards +; individualCount: +1 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Arkansas; county: Washinton; municipality: Fayetteville; locality: +University of Arkansas +; verbatimCoordinates: 36° 04' 20.24 N, 94° 10' 24.98 W; verbatimLatitude: 36° 04' 20.24 N; verbatimLongitude: 94° 10' 24.98 W; decimalLatitude: +36.072289 +; decimalLongitude: +-94.173606 +; Event: year: 2012; month: 6; day: 2; verbatimEventDate: +2.VI.2012 +; Record Level: type: PhysicalObject; language: en; institutionCode: +UAAM +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Amber D. Tripodi +; individualCount: +1 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Arkansas; county: Washinton; municipality: Fayetteville; locality: +World Peace Wetland Prairie +; decimalLatitude: +36.051894 +; decimalLongitude: +-94.172728 +; Identification: identifiedBy: Amber D. Tripodi; Event: year: 2011; month: 6; day: 29; verbatimEventDate: +Jun-29-2011 +; Record Level: type: PhysicalObject; institutionCode: +UAAM +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Clinton E. Trammel & Amber D. Tripodi +; individualCount: +1 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Florida; county: Alachua; municipality: Gainesville; locality: +University of Florida +; verbatimCoordinates: 29.650428, -82.342365; verbatimLatitude: 29.650428; verbatimLongitude: -82.342365; decimalLatitude: +29.650428 +; decimalLongitude: +-82.342365 +; Identification: identifiedBy: Amber D. Tripodi; Event: year: 2013; month: 7; day: 8; verbatimEventDate: +Jul-08-2013 +; Record Level: type: PhysicalObject; institutionCode: +BBSL +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Clinton E. Trammel & Amber D. Tripodi +; individualCount: +12 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Florida; county: Alachua; municipality: Gainesville; locality: +University of Florida +; verbatimCoordinates: 29.650428, -82.342365; verbatimLatitude: 29.650428; verbatimLongitude: -82.342365; decimalLatitude: +29.650428 +; decimalLongitude: +-82.342365 +; Identification: identifiedBy: Amber D. Tripodi; Event: year: 2013; month: 7; day: 8; verbatimEventDate: +Jul-08-2013 +; Record Level: type: PhysicalObject; institutionCode: +ADT +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Amber D. Tripodi +; individualCount: +3 +; sex: +1 male +, +2 female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Florida; county: Alachua; municipality: Gainesville; locality: +University of Florida +; verbatimCoordinates: 29.650428, -82.342365; verbatimLatitude: 29.650428; verbatimLongitude: -82.342365; decimalLatitude: +29.650428 +; decimalLongitude: +-82.342365 +; Identification: identifiedBy: Amber D. Tripodi; Event: year: 2013; month: 6; day: 21; verbatimEventDate: +Jun-21-2015 +; Record Level: type: PhysicalObject; institutionCode: +BBSL +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Amber D. Tripodi +; individualCount: +59 +; sex: +2 male +, +57 female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Florida; county: Alachua; municipality: Gainesville; locality: +University of Florida +; verbatimCoordinates: 29.650428, -82.342365; verbatimLatitude: 29.650428; verbatimLongitude: -82.342365; decimalLatitude: +29.650428 +; decimalLongitude: +-82.342365 +; Identification: identifiedBy: Amber D. Tripodi; Event: year: 2013; month: 6; day: 21; verbatimEventDate: +Jun-21-2015 +; Record Level: type: PhysicalObject; institutionCode: +ADT +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Amber D. Tripodi +; individualCount: +1 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Louisiana; county: West Feliciana; municipality: St. Francisville; decimalLatitude: +30.792733 +; decimalLongitude: +-91.249833 +; Identification: identifiedBy: Amber D. Tripodi; Event: year: 2013; month: 7; day: 4; verbatimEventDate: +Jul-04-2013 +; Record Level: type: PhysicalObject; institutionCode: +ADT +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Amber D. Tripodi +; individualCount: +1 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Michigan; county: Berrien; municipality: Watervlivet; verbatimCoordinates: 42.179430, -86.258730; verbatimLatitude: 42.179430; verbatimLongitude: -86.258730; decimalLatitude: +42.179430 +; decimalLongitude: +-86.258730 +; Identification: identifiedBy: Amber D. Tripodi; Event: year: 2015; month: 7; day: 31; verbatimEventDate: +Jul-31-2015 +; Record Level: type: PhysicalObject; institutionCode: +BBSL +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Amber D. Tripodi +; individualCount: +11 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Michigan; county: Berrien; municipality: Watervlivet; verbatimCoordinates: 42.179430, -86.258730; verbatimLatitude: 42.179430; verbatimLongitude: -86.258730; decimalLatitude: +42.179430 +; decimalLongitude: +-86.258730 +; Identification: identifiedBy: Amber D. Tripodi; Event: year: 2015; month: 7; day: 31; verbatimEventDate: +Jul-31-2015 +; Record Level: type: PhysicalObject; institutionCode: +ADT +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +M. L. Whitten +; individualCount: +3 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Grenada; municipality: Scobey; locality: +Cascilla Road +; locationRemarks: old wooden goat barn, nesting in holes made by Xylocopa; verbatimCoordinates: 33°53 +'34" +N, -89°55 +'09" +W; verbatimLatitude: 33°53 +'34" +N; verbatimLongitude: -89°55 +'09" +W; decimalLatitude: +33.892778 +; decimalLongitude: +-89.919167 +; Identification: identifiedBy: Katherine A. Parys; Event: samplingProtocol: +at large +; year: 2015; month: 7; day: 4; verbatimEventDate: +Jul-04-2015 +; Record Level: type: PhysicalObject; institutionCode: +BBSL +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +M. L. Whitten +; individualCount: +3 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Grenada; municipality: Scobey; locality: +Cascilla Road +; locationRemarks: old wooden goat barn, nesting in holes made by Xylocopa; verbatimCoordinates: 33°53 +'34" +N, -89°55 +'09" +W; verbatimLatitude: 33°53 +'34" +N; verbatimLongitude: -89°55 +'09" +W; decimalLatitude: +33.892778 +; decimalLongitude: +-89.919167 +; Identification: identifiedBy: Katherine A. Parys; Event: samplingProtocol: +at large +; year: 2015; month: 7; day: 4; verbatimEventDate: +Jul-04-2015 +; Record Level: type: PhysicalObject; institutionCode: +MEM +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +M. L. Whitten +; individualCount: +2 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Grenada; municipality: Scobey; locality: +Cascilla Road +; locationRemarks: old wooden goat barn, nesting in holes made by Xylocopa; verbatimCoordinates: 33°53 +'34" +N, -89°55 +'09" +W; verbatimLatitude: 33°53 +'34" +N; verbatimLongitude: -89°55 +'09" +W; decimalLatitude: +33.892778 +; decimalLongitude: +-89.919167 +; Identification: identifiedBy: Katherine A. Parys; Event: samplingProtocol: +at large +; year: 2015; month: 7; day: 4; verbatimEventDate: +Jul-04-2015 +; Record Level: type: PhysicalObject; institutionCode: +KAP +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: individualCount: +1 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Lafayette; municipality: Oxford; Event: year: 2005; month: 7; day: 25; verbatimEventDate: +Jul-25-2005 +; Record Level: type: PhysicalObject; institutionCode: +UMIC +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Jonas King +; individualCount: +7 +; sex: +male +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Lafayette; municipality: Oxford; locality: +University of Mississippi Campus +; locationRemarks: taken from golden raintree, Koelreuteria paniculata; Event: year: 2008; month: 4; day: 15; verbatimEventDate: +Apr-15-2008 +; Record Level: type: PhysicalObject; institutionCode: +UMIC +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Clinton E. Trammel & Amber D. Tripodi +; individualCount: +2 +; sex: +1 male +, +1 female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Lafayette; municipality: Oxford; locality: +University of Mississippi Campus +; Identification: identifiedBy: Amber D. Tripodi; Event: year: 2013; month: 7; day: 12; verbatimEventDate: +Jul-12-2013 +; Record Level: type: PhysicalObject; institutionCode: +BBSL +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Clinton E. Trammel & Amber D. Tripodi +; individualCount: +4 +; sex: +2 male +, +2 female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Lafayette; municipality: Oxford; locality: +University of Mississippi Campus +; decimalLatitude: +34.365225 +; decimalLongitude: +-89.534050 +; Identification: identifiedBy: Amber D. Tripodi; Event: year: 2013; month: 7; day: 12; verbatimEventDate: +Jul-12-2013 +; Record Level: type: PhysicalObject; institutionCode: +ADT +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +John Austin Coleman and Severino Signa +; individualCount: +1 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Tallahatchie; municipality: Paynes; locality: +Shook Rd and Hwy 35 +; Identification: identifiedBy: Katherine A. Parys; Event: samplingProtocol: +Bycatch in pheromone trap for moths +; year: 2015; month: 5; day: 23; verbatimEventDate: +May-23-2015 +; Record Level: type: PhysicalObject; institutionCode: +MEM +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Katherine A. Parys and Nathan S. Little +; individualCount: +2 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Tallahatchie; municipality: Paynes; locationRemarks: old pig barn, nesting in holes made by Xylocopa; verbatimCoordinates: 33°55 +'29" +N, -90°03 +'53" +W; verbatimLatitude: 33°55 +'29" +N; verbatimLongitude: -90°03 +'53" +W; decimalLatitude: +33.924722 +; decimalLongitude: +-90.064722 +; Identification: identifiedBy: Katherine A. Parys; Event: samplingProtocol: +by net +; year: 2015; month: 7; day: 6; verbatimEventDate: +Jul-06-2015 +; Record Level: type: PhysicalObject; institutionCode: +BBSL +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Katherine A. Parys and Nathan S. Little +; individualCount: +2 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Tallahatchie; municipality: Paynes; locationRemarks: old pig barn, nesting in holes made by Xylocopa; verbatimCoordinates: 33°55 +'29" +N, -90°03 +'53" +W; verbatimLatitude: 33°55 +'29" +N; verbatimLongitude: -90°03 +'53" +W; decimalLatitude: +33.924722 +; decimalLongitude: +-90.064722 +; Identification: identifiedBy: Katherine A. Parys; Event: samplingProtocol: +by net +; year: 2015; month: 7; day: 6; verbatimEventDate: +Jul-06-2015 +; Record Level: type: PhysicalObject; institutionCode: +MEM +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +JoVonn G. Hill +; individualCount: +2 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Oktibbeha; locality: +3 mi East of Starkville +; locationRemarks: Collected in Vitex agnus-castus flowers; verbatimCoordinates: + +33°25 +'47" +N + +, - + +88°44 +'01" +W + +; verbatimLatitude: + +33°25 +'47" +N + +; verbatimLongitude: - + +88°44 +'01" +W + +; Event: year: 2008; month: 7; day: 20; verbatimEventDate: +Jul-20-2008 +; Record Level: type: PhysicalObject; institutionCode: +MEM +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +JoVonn G. Hill +; individualCount: +2 +; sex: +1 male +, +1 female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Oktibbeha; locality: +3 mi East of Starkville +; locationRemarks: Collected in Vitex agnus-castus flowers; verbatimCoordinates: + +33°25 +'47" +N + +, - + +88°44 +'01" +W + +; verbatimLatitude: + +33°25 +'47" +N + +; verbatimLongitude: - + +88°44 +'01" +W + +; Event: year: 2008; month: 7; day: 27; verbatimEventDate: +Jul-27-2008 +; Record Level: type: PhysicalObject; institutionCode: +MEM +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +JoVonn G. Hill +; individualCount: +5 +; sex: +male +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Oktibbeha; locality: +3 mi East of Starkville +; locationRemarks: Collected in Vitex agnus-castus flowers; verbatimCoordinates: + +33°25 +'47" +N + +, - + +88°44 +'01" +W + +; verbatimLatitude: + +33°25 +'47" +N + +; verbatimLongitude: - + +88°44 +'01" +W + +; Event: year: 2008; month: 7; day: 29; verbatimEventDate: +Jul-29-2008 +; Record Level: type: PhysicalObject; institutionCode: +MEM +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Christopher T. Werle +; individualCount: +3 +; sex: +male +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Pear River; municipality: McNeill; locationRemarks: emerged from wooden trap nests, 3/8" holes; Identification: identifiedBy: Blair J. Sampson; Event: samplingProtocol: +wooden trap nests, 3/8" holes +; year: 2011; month: 7; day: 2-7; verbatimEventDate: +VI-2-7-2011 +; Record Level: type: PhysicalObject; institutionCode: +MEM +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Christopher T. Werle +; individualCount: +4 +; sex: +male +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Pear River; municipality: McNeill; locationRemarks: emerged from wooden trap nests, 3/8" holes; Identification: identifiedBy: Blair J. Sampson; Event: samplingProtocol: +wooden trap nests, 3/8" holes +; year: 2011; month: 7; day: 2-7; verbatimEventDate: +VI-2-7-2011 +; Record Level: type: PhysicalObject; institutionCode: +BJS +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Ruth Tierce +; individualCount: +2 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Yalobusha; locality: +4 mi NE of Coffeeville +; locationRemarks: on back door of house; Event: samplingProtocol: +at large +; year: 2004; month: 8; day: 6; verbatimEventDate: +IIX-6-2004 +; Record Level: type: PhysicalObject; institutionCode: +MEM +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +C. Zirkle +; individualCount: +1 +; sex: +male +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Missouri; county: Barry; locationRemarks: cleared ridge top for cattle grazing, Flowering plants nearby: water hemlock, poke, mullein, blackberries, and Ozark chinquapin; verbatimCoordinates: N36°37'54.770" W93°49'05.382"; verbatimLatitude: N36°37'54.770"; verbatimLongitude: W93°49'05.382"; decimalLatitude: +36.631881 +; decimalLongitude: +-93.818162 +; Event: samplingProtocol: +blue vane trap +; year: 2015; verbatimEventDate: +June 28- July 3, 2015 +; Record Level: type: PhysicalObject; institutionCode: +UAAM +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +C. Zirkle +; individualCount: +2 +; sex: +1 male +, +1 female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Missouri; county: Barry; locationRemarks: cleared ridge top for cattle grazing, Flowering plants nearby: water hemlock and Ozark chinquapin; verbatimCoordinates: N36°37'38.993" W93°49'11.257"; verbatimLatitude: N36°37'38.993"; verbatimLongitude: W93°49'11.257"; decimalLatitude: +36.627498 +; decimalLongitude: +-93.819794 +; Event: samplingProtocol: +blue vane trap +; year: 2015; month: 6; verbatimEventDate: +June 21 - 28, 2015 +; Record Level: type: PhysicalObject; institutionCode: +UAAM +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Bruce Schutte +; individualCount: +1 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Missouri; county: Lincoln; locality: +Cuivre River State Park +; Identification: identifiedBy: Mike Arduser; Event: year: 2006; month: 6; verbatimEventDate: +Jun-2006 +; Record Level: type: PhysicalObject; institutionCode: +MA +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Mike Arduser +; individualCount: +1 +; sex: +male +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Missouri; county: Pettis; municipality: Drover's Prairie; locality: +South of Sedalia about 10 miles +; Identification: identifiedBy: Mike Arduser; Event: year: 2010; month: 7; day: 10; verbatimEventDate: +Jul-10-2010 +; Record Level: type: PhysicalObject; institutionCode: +MA +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +George Diehl Jr. & Mike Arduser +; individualCount: +1 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Missouri; county: St. Louis; municipality: St. Louis City; locality: +City Museum +; locationRemarks: emerged from old log house; Identification: identifiedBy: Mike Arduser; Event: year: 2004; month: 7; day: 5; verbatimEventDate: +Jul-05-2004 +; Record Level: type: PhysicalObject; institutionCode: +MA +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Jane Stevens +; individualCount: +1 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Missouri; county: St. Louis; municipality: St. Louis City; locality: +St. Louis Zoo +; Identification: identifiedBy: Mike Arduser; Event: year: 2007; month: 6; verbatimEventDate: +Jun-2007 +; Record Level: type: PhysicalObject; institutionCode: +MA +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Zach Scott +; individualCount: +1 +; sex: +male +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Rhode Island; county: Washington; municipality: Kingston; locality: +University of Rhode Island East Farm +; decimalLatitude: +31.620610 +; decimalLongitude: +-94.647550 +; Identification: identifiedBy: Zach Scott; Event: year: 2014; month: 7; day: 30; verbatimEventDate: +Jul-30-2014 +; Record Level: type: PhysicalObject; institutionCode: +ZS +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +A. Hays +; individualCount: +1 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Tennessee; county: Henderson; municipality: Lexington; locationRemarks: taken in back yard; decimalLatitude: +35.681934 +; decimalLongitude: +-88.365206 +; Event: samplingProtocol: +By Hand, In Yard +; year: 2015; month: 6; day: 22; verbatimEventDate: +Jun-22-2015 +; Record Level: type: PhysicalObject; institutionCode: +BBSL +; basisOfRecord: PreservedSpecimen; informationWithheld: Street Address + + + + +Type status: +Other material +. Occurrence: recordedBy: +Beverly A. Smith +; individualCount: +1 +; sex: +female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Tennessee; county: Rutherford; locality: +Stone's River Glade +; locationRemarks: Collected on Rudbeckia sp. in cedar glade; verbatimCoordinates: 35°52'24" N 86°26'09" W; verbatimLatitude: 35°52'24" N; verbatimLongitude: 86°26'09" W; decimalLatitude: +35.873333 +; decimalLongitude: +-86.435833 +; Event: year: 2009; month: 7; day: 23; verbatimEventDate: +VII-23-2009 +; Record Level: type: PhysicalObject; institutionCode: +MEM +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Dan Bennett +; individualCount: +2 +; sex: +1 male +, +1 female +; lifeStage: +adult +; occurrenceStatus: present; preparations: whole animal (pinned); disposition: in collection; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Texas; county: Nacogdoches; locality: +Steven F. Austin State University Campus +; verbatimElevation: 97 m; locationRemarks: on Vitex agnus-castus flowers (chaste tree); verbatimCoordinates: 31.62061°; - 94.64755°; verbatimLatitude: 31.62061°; verbatimLongitude: -94.64755°; decimalLatitude: +31.620610 +; decimalLongitude: +-94.647550 +; Identification: identifiedBy: Dan Bennett; Record Level: type: PhysicalObject; institutionCode: +SFAC +; basisOfRecord: PreservedSpecimen + + + + +Type status: +Other material +. Occurrence: recordedBy: +Richard Brown +; individualCount: +1 +; lifeStage: +adult +; occurrenceStatus: present; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Noxubee; locality: +Noxubee National Wildlife Refuge +; Record Level: type: Event; basisOfRecord: HumanObservation + + + + +Type status: +Other material +. Occurrence: recordedBy: +John Pascarella +; individualCount: +1 +; lifeStage: +adult +; occurrenceStatus: present; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Texas; county: Huntsville; locality: +Sam Houston State University +; Event: year: 2014; month: 7; Record Level: type: Event; basisOfRecord: HumanObservation + + + + +Type status: +Other material +. Occurrence: recordedBy: +Jeff Harris +; individualCount: +1 +; lifeStage: +adult +; occurrenceStatus: present; Taxon: scientificName: Megachilesculpturalis Smith, 1853; kingdom: Animalia; phylum: Arthropoda; class: Insecta; order: Hymenoptera; family: Megachilidae; genus: Megachile; subgenus: Callomegachile; specificEpithet: sculpturalis; scientificNameAuthorship: Smith, 1853; vernacularName: Giant Resin Bee; nomenclaturalCode: ICZN; taxonomicStatus: accepted; Location: continent: North America; country: +United States +; countryCode: US; stateProvince: Mississippi; county: Neshoba; municipality: Philadelphia; Event: year: 2015; month: 7; Record Level: type: Event; basisOfRecord: HumanObservation + + + + +Distribution + +Specimen and observational data presented here expand the known distribution of +M. sculpturalis +to every state east of the Mississippi River and several western states including Arkansas, Iowa, Kansas, Louisiana, Missouri, Nebraska, and Texas (Fig. 2). + +Hinojosa-Diaz +et al. (2005) + +used niche modeling to predict the expansion of the range in the United States, and current data continue to support that model (e.g., Hinojosa-Diaz 2008). While specimen records had previously been reported from Tennessee in the literature ( +Mangum and Sumner 2003 +), the records presented were in the far eastern portion of the state. Museum records now extend the distribution west within the state and include +Rudbeckia +sp. ( +Asteraceae +/ +Compositae +) as a new floral host from specimen data presented here. Record of +M. sculpturalis +from Rhode Island was anecdotally mentioned in +Maier (2005) +but never confirmed with collected specimens. The first record of +M. sculpturalis +west of the Mississippi River dates to 2004 (♀, St. Louis, MO) and is reported here for the first time. An examination of collections from Oklahoma did not yield any records in that state, in spite of records nearby in Arkansas, Missouri, and Texas. Records presented here and in other manuscripts show clear geographic expansion over time (Fig. 3), but it appears that the formal documentation of records lags behind the actual expansion. + + + + \ No newline at end of file diff --git a/data/38/EA/88/38EA8842A5FC03FBF9FE965074B5AD9B.xml b/data/38/EA/88/38EA8842A5FC03FBF9FE965074B5AD9B.xml new file mode 100644 index 00000000000..9a6cc465f3c --- /dev/null +++ b/data/38/EA/88/38EA8842A5FC03FBF9FE965074B5AD9B.xml @@ -0,0 +1,85 @@ + + + +Description of a new species of weasel shark, Hemigaleus australiensis n. sp. (Carcharhiniformes: Hemigaleidae) from Australian waters. + + + +Author + +William T. White + + + +Author + +Peter R. Last + + + +Author + +Leonard J. V. Compagno + +text + + +Zootaxa + + +2005 + +1077 + + +37 +49 + + + + +http://www.zoobank.org/urn:lsid:zoobank.org:pub:07CAF72E-7644-4F71-9A42-241945FC52D3 + +journal article +z01077p037 + + + + +[[ +Hemigaleus Bleeker +]] + + + + +The genus +Hemigaleus +, proposed by Bleeker (1852) for +Hemigaleus microstoma +from Java, presently consists of only one described species. +Hemigaleus microstoma +is widely distributed in the Indo-West Pacific from southern India and Sri Lanka in the west, to Myanmar, Thailand, Indonesia (Java), Taiwan, China and the Philippines in the east (Compagno, 1984, 1988, 1998). This species was also previously documented as occurring widely across northern Australia (Compagno, 1984), and off Papua New Guinea (Last and Stevens, 1994). Stevens and Cuthbert (1983) documented substantial differences in tooth and vertebral counts between Australian specimens and material from Singapore, Thailand and Indonesia (see also Compagno, 1988). These authors provisionally identified the Australian form as +H. microstoma +but stated that a revision of the genus should be undertaken in the future once specimens were collected from other areas. Similarly, Compagno (1988) treated +Hemigaleus +temporarily as a monotypic genus, but stated that the observed differences between the specimens could be elucidated once more specimens were examined from other regions. Last and Stevens (1994) highlighted the need for a comparison of material from across the Indo-Pacific region to explain morphological differences in +Hemigaleus +populations. Compagno (1999) stated that differences in coloration and meristics suggest that the Australian species may be a separate taxon and he treated the two separate forms in the key to species, i.e. +Hemigaleus microstoma +and +H. sp. aff. “microstoma” +. + + +Recent market surveys in eastern Indonesia produced a variety of sharks, skates, rays and chimaeras. Amongst this material were a number of individuals of +Hemigaleus microstoma +. These specimens have allowed a more detailed comparison between the Australian and Indonesian samples and have confirmed that the Australian +Hemigaleus +is a separate species from +H. microstoma +. This new species is described below. + + + + \ No newline at end of file diff --git a/data/38/EB/4C/38EB4C73A27DA4DDE219C47576419BF7.xml b/data/38/EB/4C/38EB4C73A27DA4DDE219C47576419BF7.xml new file mode 100644 index 00000000000..d9cb1abc7fe --- /dev/null +++ b/data/38/EB/4C/38EB4C73A27DA4DDE219C47576419BF7.xml @@ -0,0 +1,138 @@ + + + +Aquatic Insects from the Caatinga: checklists and diversity assessments of Ubajara (Ceara State) and Sete Cidades (Piaui State) National Parks, Northeastern Brazil + + + +Author + +Takiya, Daniela Maeda + + + +Author + +Santos, Allan Paulo Moreira + + + +Author + +Pinto, Angelo Parise + + + +Author + +Henriques-Oliveira, Ana Lucia + + + +Author + +Carvalho, Alcimar do Lago + + + +Author + +Sampaio, Brunno Henrique Lanzellotti + + + +Author + +Clarkson, Bruno + + + +Author + +Moreira, Felipe Ferraz Figueiredo + + + +Author + +Avelino-Capistrano, Fernanda + + + +Author + +Goncalves, Ines Correa + + + +Author + +Cordeiro, Isabelle da Rocha Silva + + + +Author + +Camara, Josenir Teixeira + + + +Author + +Barbosa, Julianna Freires + + + +Author + +de Souza, W. Rafael Maciel + + + +Author + +Rafael, Jose Albertino + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8354 +8354 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8354 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8354 +1314-2828-4-8354 + + + + + +Limnogonus +Stal +, 1868 + + + + +Notes + +Genus firstly recorded from CE in +Cordeiro and Moreira 2015 +. + + + + \ No newline at end of file diff --git a/data/38/EB/7C/38EB7C98A0A89D2AB1262366F5E4278B.xml b/data/38/EB/7C/38EB7C98A0A89D2AB1262366F5E4278B.xml new file mode 100644 index 00000000000..48c29e48bc7 --- /dev/null +++ b/data/38/EB/7C/38EB7C98A0A89D2AB1262366F5E4278B.xml @@ -0,0 +1,85 @@ + + + +Taxonomic and morphological survey of the Lygephila lusoria (Linnaeus, 1758) species-group with description of a new species (Lepidoptera, Erebidae, Toxocampinae) + + + +Author + +Pekarsky, Oleg + +text + + +ZooKeys + + +2013 + +351 + + +49 +81 + + + + +http://dx.doi.org/10.3897/zookeys.351.5999 + +journal article +http://dx.doi.org/10.3897/zookeys.351.5999 +1313-2970-351-49 +51D02BF632034105A73F498F39A01106 + + + + +Lygephila fereidun Wiltshire, 1961 +Fig. 18 + + + +Taxonomy. + +This taxon, described from the Elburz Mountains, Northern Iran, is known only from the holotype (coll. BMNH). In the original description the color was characterized as pale straw and the wing pattern close to the Spanish species glycyrrhizae. The diagnostic comparison was made with +Lygephila craccae +([Denis & +Schiffermueller +], 1775) and +Lygephila lusoria +only, whereas a comparison with another similar species, +Lygephila pallida +,was neglected. The original description contains the following text about the clasping apparatus structure (Fig. 28): "The harpe [ampulla], longer than that of craccae, is nevertheless shorter than that of lusoria." Comparative analysis of the ampullar length (shorter than that of lusoria) given by Wiltshire, makes it possible to conclude that the +Lygephila fereidun +is different from the +Lygephila amasina +and +Lygephila subpicata +, because they have longer ampullae that reach the costal margin of the valva. So, by this feature +Lygephila fereidun +could be compared only with +Lygephila pallida +,the ampulla of which is rather shorter than that of +Lygephila lusoria +and other members of its species group. Vesica structure in the original description is characterized as follows: "The vesica contains similar elements to those of lusoria but the proximal scobinated field is shorter and the five or six teeth on the distal chitinous lump are larger and more like cornuti than in lusoria." However, the only sclerotized cornutus formation illustrated in the original drawing looks similar to that of +Lygephila subpicata +, but +Lygephila subpicata +has two heavily-sclerotized crown-like cornuti on the top of subbasal and 2nd medial diverticula. + + +The above-mentioned contradictions in the original description thereby make it impossible to clarify the taxonomical situation of this taxon without a study of the genitalia of the holotype, the preparation of which is opaque and requires specific recovery treatment. Based on the currently known characters +Lygephila fereidun +is most likely an aberrant specimenof +Lygephila pallida +. + + + +Distribution. +Northern Iran. + + + \ No newline at end of file diff --git a/data/38/EB/91/38EB91B5CAB6469A32C8E9CC724C80AB.xml b/data/38/EB/91/38EB91B5CAB6469A32C8E9CC724C80AB.xml new file mode 100644 index 00000000000..26a134ec441 --- /dev/null +++ b/data/38/EB/91/38EB91B5CAB6469A32C8E9CC724C80AB.xml @@ -0,0 +1,52 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828--9042 + + + + +Picrostigeus recticauda (Thomson, 1897) + + + + +Orthocentrus recticauda +Thomson, 1897 + + + +Distribution +England, Scotland, Wales, Ireland + + + \ No newline at end of file diff --git a/data/38/EB/AD/38EBAD378E1E77E3D9C90279E01FAFD9.xml b/data/38/EB/AD/38EBAD378E1E77E3D9C90279E01FAFD9.xml new file mode 100644 index 00000000000..cbdb5098b58 --- /dev/null +++ b/data/38/EB/AD/38EBAD378E1E77E3D9C90279E01FAFD9.xml @@ -0,0 +1,350 @@ + + + +Info Flora Schweiz - Brassicaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/brassicaceae.html + +url + + + + + +Erysimum rhaeticum +(Hornem.) DC. + + + + + + +Schweizer +Schoeterich + + + + + +Art ISFS: 158490 Checklist: 1017980 +Brassicaceae +Erysimum +Erysimum rhaeticum +aggr. +Erysimum rhaeticum (Hornem.) DC. + + +Zusammenfassung +KEINE ANGABE + + + +Status Nationale +Prioritaet + +: -- + + +Internationale Verantwortung +: -- Erhalten/ +Foerdern +Gefaehrdungen +Keine besonderen +Gefaehrdungen +(Art ist in der Schweiz nicht im +Rueckgang +) + + + +Oekologie + + + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + +KEINE ANGABE + + +
+
+
+
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F--Lichtzahl L--Salzzeichen--
Reaktionszahl R--Temperaturzahl T--
+Naehrstoffzahl +N +-- +Kontinentalitaetszahl +K +--
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Erysimum rhaeticum +(Hornem.) DC. + + + + + + +Volksname Deutscher Name: + +Schweizer +Schoeterich + +, +Schweizerischer Schotendotter +, + +Schweizerischer +Schoeterich + +Nom +francais +: + +Velar +de Suisse + +, + +Erysimum +de Suisse + +, + +Erysimum +rhetique + + + + +Nome italiano: -- + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Erysimum rhaeticum (Hornem.) DC. + + +Checklist 2017 + +158490
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Kommentare aus der +Checklist 2017 +Neues Konzept: Die Art ist +gegenueber +SISF-2 enger gefasst, da +E. insubricum +Peccenini & Polatschek, + +E. jugicola +Jord. + +und + +E. sylvestre +(Crantz) Scop. + +abgetrennt wurden. Checklist + + + + +Status Indigenat +: Indigen + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein Status Rote Liste national + + + + + + +
KEINE ANGABE
+
+ + +Status nationale +Prioritaet +/Verantwortung + + + + + + + + + + + + + + + + + + + + + + + + + +
+ +Nationale +Prioritaet + +--
+Massnahmenbedarf +--
+ +Internationale Verantwortung + +--
+ +Ueberwachung +Bestaende + +--
+ +Schutzstatus + + + + + + +
Kein internationaler, nationaler oder kantonaler Schutz
+
+
+
+
\ No newline at end of file diff --git a/data/38/EC/28/38EC28CB2078F31C7F22AC164E9B285F.xml b/data/38/EC/28/38EC28CB2078F31C7F22AC164E9B285F.xml new file mode 100644 index 00000000000..ed09fe16678 --- /dev/null +++ b/data/38/EC/28/38EC28CB2078F31C7F22AC164E9B285F.xml @@ -0,0 +1,88 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part A) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +252 +342 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Avena flavescens +Linnaeus + +, + +Species Plantarum +1 + +: 80. 1753 + + +. + + + +"Habitat in Germania, Anglia, Gallia." RCN: 673. + + + + +Lectotype +(Cope in Cafferty & al. in +Taxon +49: 247. 2000): Herb. A. van Royen No. 913.7-458 ( +L +) + +. + + + + +Current name: + + +Trisetum flavescens + +(L.) P. Beauv. + +( +Poaceae +). + + + + \ No newline at end of file diff --git a/data/38/EC/36/38EC364B4E280E2E2145925775CC8ABF.xml b/data/38/EC/36/38EC364B4E280E2E2145925775CC8ABF.xml new file mode 100644 index 00000000000..facb595b5a2 --- /dev/null +++ b/data/38/EC/36/38EC364B4E280E2E2145925775CC8ABF.xml @@ -0,0 +1,65 @@ + + + +Checklist of British and Irish Hymenoptera - Platygastroidea + + + +Author + +Buhl, Peter N. + + + +Author + +Broad, Gavin R. + + + +Author + +Notton, David G. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +7991 +7991 + + + + +http://dx.doi.org/10.3897/BDJ.4.e7991 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e7991 +1314-2828-4-7991 + + + + +Euxestonotus hasselbalchi Buhl, 1995 + + + +Distribution +England, Wales, Ireland, Isle of Man + + +Notes + +added by +Buhl (1995b) + + + + \ No newline at end of file diff --git a/data/38/EC/63/38EC6377696EFDDC932D6C8AAA53283D.xml b/data/38/EC/63/38EC6377696EFDDC932D6C8AAA53283D.xml new file mode 100644 index 00000000000..6a11c5dd81a --- /dev/null +++ b/data/38/EC/63/38EC6377696EFDDC932D6C8AAA53283D.xml @@ -0,0 +1,81 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part A) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +252 +342 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Aster oppositifolius +Linnaeus + +, + +Systema Naturae +, ed. 10, 2 + +: 1216. 1759 + + +. + + + +RCN: 6372. + + +Type not designated. + + +Original material: [icon] in Miller, Fig. Pl. Gard. Dict. 1: 51, t. 76, f. 2. 1756. + + + +Current name: + + +Felicia cymbalariae + +(Aiton) Bolus & Wolley-Dod + +( +Asteraceae +). + + + + \ No newline at end of file diff --git a/data/38/EC/A6/38ECA6347CAAB72C6AD38E1CC1982DFD.xml b/data/38/EC/A6/38ECA6347CAAB72C6AD38E1CC1982DFD.xml new file mode 100644 index 00000000000..cc4845b8d2c --- /dev/null +++ b/data/38/EC/A6/38ECA6347CAAB72C6AD38E1CC1982DFD.xml @@ -0,0 +1,138 @@ + + + +Checklist of Serengeti Ecosystem Grasses + + + +Author + +Williams, Emma Victoria + + + +Author + +Elia Ntandu, John + + + +Author + +Ficinski, Pawel + + + +Author + +Vorontsova, Maria + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +8286 +8286 + + + + +http://dx.doi.org/10.3897/BDJ.4.e8286 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e8286 +1314-2828--8286 + + + + +Echinochloa colona (L.) Link + + + +Materials + + +Type status: +Other material +. Occurrence: catalogNumber: +602 +; recordNumber: s.n.; recordedBy: +Mboya, E +; Taxon: scientificName: Echinochloacolona (L.) Link; kingdom: Plantae; family: Poaceae; genus: Echinochloa; specificEpithet: colona; scientificNameAuthorship: (L.) Link; Location: continent: Africa; country: +Tanzania +; stateProvince: Mara; county: Serengeti; locality: +Seronera Lodge +; verbatimLocality: T1. Area around Frankfurt Zoological Society Headquarters and Seronera Lodge.; minimumElevationInMeters: 1512; decimalLatitude: +-2.44 +; decimalLongitude: +34.82 +; Event: eventDate: +2004-02-09 +; Record Level: institutionCode: +MO +; collectionCode: +Herbarium +; ownerInstitutionCode: MO; basisOfRecord: PreservedSpecimen + + +Type status: +Other material +. Occurrence: catalogNumber: +603 +; recordNumber: s.n.; recordedBy: +Mboya, E +; Taxon: scientificName: Echinochloacolona (L.) Link; kingdom: Plantae; family: Poaceae; genus: Echinochloa; specificEpithet: colona; scientificNameAuthorship: (L.) Link; Location: continent: Africa; country: +Tanzania +; stateProvince: Mara; county: Serengeti; locality: +Serengeti National Park +; verbatimLocality: T1. Serengeti National Park. Ndabaka-Seronera Road.; minimumElevationInMeters: 1297; decimalLatitude: +-2.27 +; decimalLongitude: +34.58 +; Event: eventDate: +2004-03-09 +; Record Level: institutionCode: +MO +; collectionCode: +Herbarium +; ownerInstitutionCode: MO; basisOfRecord: PreservedSpecimen + + +Type status: +Other material +. Occurrence: catalogNumber: +604 +; recordNumber: s.n.; recordedBy: +Mboya, E +; Taxon: scientificName: Echinochloacolona (L.) Link; kingdom: Plantae; family: Poaceae; genus: Echinochloa; specificEpithet: colona; scientificNameAuthorship: (L.) Link; Location: continent: Africa; country: +Tanzania +; stateProvince: Mara; county: Serengeti; locality: +Serengeti Research Centre +; verbatimLocality: T1. Serengeti Research Centre.; minimumElevationInMeters: 1548; decimalLatitude: +-2.38 +; decimalLongitude: +34.85 +; Event: eventDate: +2004-03-12 +; Record Level: institutionCode: +MO +; collectionCode: +Herbarium +; ownerInstitutionCode: MO; basisOfRecord: PreservedSpecimen + + + + +Distribution +Widespread + + + \ No newline at end of file diff --git a/data/38/EC/E4/38ECE44831C15881ABFB21B4F172A1EE.xml b/data/38/EC/E4/38ECE44831C15881ABFB21B4F172A1EE.xml new file mode 100644 index 00000000000..d2d6fbcae34 --- /dev/null +++ b/data/38/EC/E4/38ECE44831C15881ABFB21B4F172A1EE.xml @@ -0,0 +1,125 @@ + + + +Distribution of wild bee (Hymenoptera: Anthophila) and hoverfly (Diptera: Syrphidae) communities within farms undergoing ecological transition + + + +Author + +Noel, Gregoire +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium +gregoire.noel@uliege.be + + + +Author + +Bonnet, Julie +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + + + +Author + +Everaerts, Sylvain +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + + + +Author + +Danel, Anouk +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + + + +Author + +Calderan, Alix +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + + + +Author + +de Liedekerke, Alexis +Ferme de Froidefontaine, Havelange, Belgium + + + +Author + +de Montpellier d'Annevoie, Clotilde +Department of Geography, Institute Transitions, University of Namur, Namur, Belgium & Ferme d'Emeville, Havelange, Belgium + + + +Author + +Francis, Frederic +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + + + +Author + +Serteyn, Laurent +Functional and Evolutionary Entomology, Gembloux Agro-Bio Tech - University of Liege, TERRA, Gembloux, Belgium + +text + + +Biodiversity Data Journal + + +2021 + +2021-01-14 + + +9 + + +60665 +60665 + + + + +http://dx.doi.org/10.3897/BDJ.9.e60665 + +journal article +http://dx.doi.org/10.3897/BDJ.9.e60665 +1314-2828-9-e60665 +A14A82B6E4E456E6AA051CADA0ECE3E6 + + + + +Chelostoma rapunculi (Lepeletier 1841) + + + +Ecological interactions + + +Feeds on + +Oligolectic on +Campanulaceae + + + +Conservation status +Least Concern + + +Notes + +Table +2 + + + + \ No newline at end of file diff --git a/data/38/ED/22/38ED22D4438258D5482A88E575310BC3.xml b/data/38/ED/22/38ED22D4438258D5482A88E575310BC3.xml new file mode 100644 index 00000000000..5c1e6f43238 --- /dev/null +++ b/data/38/ED/22/38ED22D4438258D5482A88E575310BC3.xml @@ -0,0 +1,833 @@ + + + +Biodiversity inventories in high gear: DNA barcoding facilitates a rapid biotic survey of a temperate nature reserve + + + +Author + +Telfer, Angela C +Biodiversity Institute of Ontario, Guelph, Canada +atelfer@uoguelph.ca + + + +Author + +Young, Monica R +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Quinn, Jenna +rare Charitable Research Reserve, Cambridge, Canada + + + +Author + +Perez, Kate +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Sobel, Crystal N +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Sones, Jayme E +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Levesque-Beaudin, Valerie +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Derbyshire, Rachael +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Fernandez-Triana, Jose +CNC, Ottawa, Canada +https://orcid.org/0000-0003-0425-0309 + + + +Author + +Rougerie, Rodolphe +Museum national d'Histoire Naturelle, Paris, France + + + +Author + +Thevanayagam, Abinah +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Boskovic, Adrian +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Borisenko, Alex V +Biodiversity Institute of Ontario, Guelph, Canada +https://orcid.org/0000-0002-3061-3057 + + + +Author + +Cadel, Alex +University of Waterloo, Waterloo, Canada + + + +Author + +Brown, Allison +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Pages, Anais +Universite de Montpellier, Montpellier, France + + + +Author + +Castillo, Anibal H +Biodiversity Institute of Ontario, Guelph, Canada +https://orcid.org/0000-0002-1537-0528 + + + +Author + +Nicolai, Annegret +EcoBio, Universite of Rennes, Rennes, France + + + +Author + +Glenn Mockford, Barb Mockford +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Bukowski, Belen +Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " (MACN-CONICET), Buenos Aires, Argentina + + + +Author + +Wilson, Bill +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Trojahn, Brock +rare Charitable Research Reserve, Cambridge, Canada + + + +Author + +Lacroix, Carole Ann +Biodiversity Institute of Ontario Herbarium, Guelph, Canada + + + +Author + +Brimblecombe, Chris +University of Waikato, Hamilton, New Zealand + + + +Author + +Hay, Christoper +University of Western Ontario, London, Canada + + + +Author + +Ho, Christmas +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Steinke, Claudia +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Warne, Connor P +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Garrido Cortes, Cristina +University of Guelph, Guelph, Canada + + + +Author + +Engelking, Daniel +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Wright, Danielle +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Lijtmaer, Dario A +Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " (MACN-CONICET), Buenos Aires, Argentina + + + +Author + +Gascoigne, David +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Hernandez Martich, David +Universidad Autonoma de Santo Domingo DR, Santo Domingo, Dominican Republic + + + +Author + +Morningstar, Derek +Myotistar, Cambridge, Canada + + + +Author + +Neumann, Dirk +SNSB, Zoologische Staatssammlung Muenchen, Munich, Germany + + + +Author + +Steinke, Dirk +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Marco DeBruin, Donna DeBruin +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Dobias, Dylan +University of Guelph, Guelph, Canada + + + +Author + +Sears, Elizabeth +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Richard, Ellen +University of Guelph, Guelph, Canada + + + +Author + +Damstra, Emily +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Zakharov, Evgeny V +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Laberge, Frederic +University of Guelph, Guelph, Canada + + + +Author + +Collins, Gemma E +University of Waikato, Hamilton, New Zealand + + + +Author + +Blagoev, Gergin A +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Grainge, Gerrie +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Ansell, Graham +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Meredith, Greg +Grand River Conservation Authority, Guelph, Canada + + + +Author + +Hogg, Ian +University of Waikato, Hamilton, New Zealand + + + +Author + +McKeown, Jaclyn +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Topan, Janet +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Bracey, Jason +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Guenther, Jerry +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Sills-Gilligan, Jesse +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Addesi, Joseph +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Persi, Joshua +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Layton, Kara K S +The University of Western Australia, Perth, Australia + + + +Author + +D'Souza, Kareina +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Dorji, Kencho +National Biodiversity Centre, Thimphu, Bhutan + + + +Author + +Grundy, Kevin +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Nghidinwa, Kirsti +Ministry of Environment and Tourism in Namibia, Windhoek, Namibia + + + +Author + +Ronnenberg, Kylee +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Lee, Kyung Min +University of Oulu, Oulu, Finland + + + +Author + +Xie, Linxi +The University of Western Ontario, London, Canada + + + +Author + +Lu, Liuqiong +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Penev, Lyubomir +Pensoft, Sofia, Bulgaria +https://orcid.org/0000-0002-2186-5033 + + + +Author + +Gonzalez, Mailyn +Instituto de Investigacion de Recursos Biologicos Alexander von Humboldt, Bogota, Colombia + + + +Author + +Rosati, Margaret E +Smithsonian National Museum of Natural History, Washington, United States of America + + + +Author + +Kekkonen, Mari +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Kuzmina, Maria +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Iskandar, Marianne +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Mutanen, Marko +University of Oulu, Oulu, Finland + + + +Author + +Fatahi, Maryam +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Pentinsaari, Mikko +University of Oulu, Oulu, Finland + + + +Author + +Bauman, Miriam +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Nikolova, Nadya +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Ivanova, Natalia V +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Jones, Nathaniel +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Weerasuriya, Nimalka +The University of Western Ontario, London, Canada + + + +Author + +Monkhouse, Norman +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Lavinia, Pablo D +Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " (MACN-CONICET), Buenos Aires, Argentina + + + +Author + +Jannetta, Paul +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Hanisch, Priscila E +Museo Argentino de Ciencias Naturales " Bernardino Rivadavia " (MACN-CONICET), Buenos Aires, Argentina + + + +Author + +McMullin, R. Troy +Biodiversity Institute of Ontario Herbarium, Guelph, Canada + + + +Author + +Ojeda Flores, Rafael +Universidad Nacional Autonoma de Mexico, Mexico City, Mexico + + + +Author + +Mouttet, Raphaelle +ANSES, Laboratoire de la Sante des Vegetaux, Montferrier sur Lez, France + + + +Author + +Vender, Reid +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Labbee, Renee N +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Forsyth, Robert +New Brunswick Museum, Saint John, Canada +https://orcid.org/0000-0002-9637-0158 + + + +Author + +Lauder, Rob +London Homeopathy, London, Canada + + + +Author + +Dickson, Ross +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Kroft, Ruth +rare Charitable Research Reserve (Affiliate of), Cambridge, Canada + + + +Author + +Miller, Scott E +Smithsonian National Museum of Natural History, Washington, United States of America + + + +Author + +MacDonald, Shannon +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Panthi, Sishir +Ministry of Forests and Soil Conservation, Kathmandu, Nepal + + + +Author + +Pedersen, Stephanie +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Sobek-Swant, Stephanie +rare Charitable Research Reserve, Cambridge, Canada + + + +Author + +Naik, Suresh +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Lipinskaya, Tatsiana +Scientific and Practical Center for Bioresources, National Academy of Sciences of Belarus, Minsk, Belarus + + + +Author + +Eagalle, Thanushi +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Decaens, Thibaud +Universite de Montpellier Centre d'Ecologie Fonctionnelle et Evolutive, Montpellier, France + + + +Author + +Kosuth, Thibault +Universite de Montpellier, Montpellier, France + + + +Author + +Braukmann, Thomas +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Woodcock, Tom +rare Charitable Research Reserve, Cambridge, Canada + + + +Author + +Roslin, Tomas +University of Helsinki, Helsinki, Finland + + + +Author + +Zammit, Tony +Grand River Conservation Authority, Cambridge, Canada + + + +Author + +Campbell, Victoria +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Dinca, Vlad +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +Peneva, Vlada +Bulgarian Academy of Sciences, Sofia, Bulgaria + + + +Author + +Hebert, Paul D N +Biodiversity Institute of Ontario, Guelph, Canada + + + +Author + +deWaard, Jeremy R +Biodiversity Institute of Ontario, Guelph, Canada +dewaardj@uoguelph.ca + +text + + +Biodiversity Data Journal + + +2015 + +3 + + +6313 +6313 + + + + +http://dx.doi.org/10.3897/BDJ.3.e6313 + +journal article +http://dx.doi.org/10.3897/BDJ.3.e6313 +1314-2828-3-e6313 +FFE5FF837519E9253D17614AFFA8FFC1 +574474 + + + + +Aedes cinereus Meigen, 1818 + + + +Notes +BOLD:AAC1222 + + + \ No newline at end of file diff --git a/data/38/ED/45/38ED45FA15263A39C91F7D7593DF957F.xml b/data/38/ED/45/38ED45FA15263A39C91F7D7593DF957F.xml new file mode 100644 index 00000000000..99e9d650841 --- /dev/null +++ b/data/38/ED/45/38ED45FA15263A39C91F7D7593DF957F.xml @@ -0,0 +1,88 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part C) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +370 +473 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Cyperus fuscus +Linnaeus + +, + +Species Plantarum +1 + +: 46. 1753 + + +. + + + +"Habitat in Galliae, Germaniae, Helvetiae pratis humidis." RCN: 394. + + + + +Lectotype +(Kukkonen in Cafferty & Jarvis in +Taxon +53: 179. 2004): Herb. Burser I: 82 ( +UPS +) + +. + + + + +Current name: + + +Cyperus fuscus + +L. + +( +Cyperaceae +). + + + + \ No newline at end of file diff --git a/data/38/ED/92/38ED92FEEC057C06B7EC3905DB47B5FB.xml b/data/38/ED/92/38ED92FEEC057C06B7EC3905DB47B5FB.xml new file mode 100644 index 00000000000..ba84521700e --- /dev/null +++ b/data/38/ED/92/38ED92FEEC057C06B7EC3905DB47B5FB.xml @@ -0,0 +1,111 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part A) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +252 +342 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Allium sativum +Linnaeus + +, + +Species Plantarum +1 + +: 296. 1753 + + +. + + + +"Habitat in Sicilia." RCN: 2354. + + + + +Lectotype +(de Wilde-Duyfjes in +Taxon +22: 81. 1973): Herb. Burser III: 90 ( +UPS +) + +. + + + + +Generitype +of + +Allium +Linnaeus + +(vide Hitchcock, +Prop. Brit. Bot. +: 145. 1929). + + + + +Current name: + + +Allium sativum + +L. + +( +Liliaceae +/ +Alliaceae +). + + + + +Note: +Although de Wilde-Duyfjes indicated the Burser material as a +neotype +, it is in fact original material for the name so her choice is accepted as a lectotypification under Art. 9.8. + + + + \ No newline at end of file diff --git a/data/38/EE/E4/38EEE4EC76D5B52EC1262A279ADE49B8.xml b/data/38/EE/E4/38EEE4EC76D5B52EC1262A279ADE49B8.xml new file mode 100644 index 00000000000..540879cb637 --- /dev/null +++ b/data/38/EE/E4/38EEE4EC76D5B52EC1262A279ADE49B8.xml @@ -0,0 +1,2379 @@ + + + +A species-level taxonomic review and host associations of Glyptapanteles (Hymenoptera, Braconidae, Microgastrinae) with an emphasis on 136 new reared species from Costa Rica and Ecuador + + + +Author + +Arias-Penna, Diana Carolina + + + +Author + +Whitfield, James B. + + + +Author + +Janzen, Daniel H. + + + +Author + +Winifred Hallwachs, + + + +Author + +Dyer, Lee A. + + + +Author + +Smith, M. Alex + + + +Author + +Hebert, Paul D. N. + + + +Author + +Fernandez-Triana, Jose L. + +text + + +ZooKeys + + +2019 + +890 + + +1 +685 + + + + +http://dx.doi.org/10.3897/zookeys.890.35786 + +journal article +http://dx.doi.org/10.3897/zookeys.890.35786 +1313-2970-890-1 +FD8F695311F64DF2950F6A387340BCE5 +2691DADB7BA352BEBA377C901FC0AC97 + + + + +Glyptapanteles scottshawi Arias-Penna, sp. nov. +Figs 199 +, +200 + + + +Female. + +Body length +2.48 mm +, antenna length +3.23 mm +, fore wing length +2.77 mm +. + + + +Type material. + + + +Holotype + +COSTA RICA +• +1♀ +; 07-SRNP-66369, DHJPAR0024907; + +Area + +de +Conservacion + + +Guanacaste +, +Alajuela +, + +Sector San +Cristobal + +, + +Rio +Blanco Abajo + +; rain forest; +Malaise +; + +500 m + +; +10.90037 +, +-85.37254 +; + +25.xi.2007 + +; +DH Janzen +& +W Hallwachs +leg.; ( +CNC +) + +. + + +Paratypes + +. • 1 (0 + +, +1♂ +) (0 + +, 0 + +); 07-SRNP-67700, DHJPAR0026395; same data as for holotype except: + +07.xi.2007 + +; ( +CNC +) + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66816, DHJPAR0025354; same data as for holotype except: + +28.vii.2007 + +; ( +CNC +) + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-67611, DHJPAR0026306; same data as for holotype except: + +03.viii.2007 + +; ( +CNC +) + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 07-SRNP-67613, DHJPAR0026308; same data as for holotype except: + +03.viii.2007 + +; ( +CNC +) + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-67671, DHJPAR0026366; same data as for holotype except: + +09.viii.2007 + +; ( +CNC +) + +. • + +1 (0 + +, 0 + +) ( +1♀ +, 0 + +); 07-SRNP-67683, DHJPAR0026378; same data as for holotype except: + +09.viii.2007 + +; ( +CNC +) + +. + + + +Other material. + +Malaise-trapped material. + +COSTA RICA +: + + +Area + +de +Conservacion + + +Guanacaste + +, + +Alajuela + +, + + +Sector San +Cristobal + + +, + + +Estacion +San Gerardo + + +: • 1 (0 + +, +1♂ +) (0 + +, 0 + +); 07-SRNP-67284, DHJPAR0025822; rain forest; +Malaise +; + +575 m + +; +10.88009 +, +-85.38887 +; + +04.vii.2007 + +; +DH Janzen +& +W Hallwachs +leg. + + + + +Area +de +Conservacion +Guanacaste + +, +Alajuela +, + +Sector + + +San +Cristobal + +, + + +Rio +Blanco Abajo + + +: • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66237, DHJPAR0024775; rain forest; +Malaise +; + +500 m + +; +10.90037 +, +-85.37254 +; + +08.viii.2007 + +; +DH Janzen +& +W Hallwachs +leg. + + +• + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66267, DHJPAR0024805; same data as for preceding except: + +16.vi.2007 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 07-SRNP-66320, DHJPAR0024858; same data as for preceding except: + +27.viii.2007 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 07-SRNP-66441, DHJPAR0024979; same data as for preceding except: + +28.vii.2007 + + +. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66442, DHJPAR0024980; same as for preceding data except: +28.vii.2007 +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66485, DHJPAR0025023; same data as for preceding except: + +16.vii.2007 + + +. • + +1 ( +1♀ +, 0 + +) (0 + +, 0 + +); 07-SRNP-66495, DHJPAR0025033; same data as for preceding except: + +16.vii.2007 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66548, DHJPAR0025086; same data as for preceding except: + +05.vi.2007 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66656, DHJPAR0025194; same data as for preceding except: + +04.vii.2007 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 07-SRNP-66676, DHJPAR0025214; same data as for preceding except: + +22.vii.2007 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66690, DHJPAR0025228; same data as for preceding except: + +22.vii.2007 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66774, DHJPAR0025312; same data as for preceding except: + +16.vi.2007 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66789, DHJPAR0025327; same data as for preceding except: + +16.vi.2007 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-2857, DHJPAR0026438; same data as for preceding except: + +18.i.2008 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-2884, DHJPAR0026465; same data as for preceding except: + +30.i.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-2922, DHJPAR0026503; same data as for preceding except: + +11.ii.2008 + + +. • + +1 ( +1♀ +, 0 + +) (0 + +, 0 + +); 08-SRNP-2950, DHJPAR0026531; same data as for preceding except: + +17.ii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-2951, DHJPAR0026532; same data as for preceding except: + +17.ii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-2954, DHJPAR0026535; same data as for preceding except: + +17.ii.2008 + + +. • + +1 (0 + +, 0 + +) ( +1♀ +, 0 + +); 08-SRNP-2963, DHJPAR0026544; same data as for preceding except: + +17.ii.2008 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-2969, DHJPAR0026550; same data as for preceding except: + +23.ii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-2978, DHJPAR0026559; same data as for preceding except: + +23.ii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-2982, DHJPAR0026563; same data as for preceding except: + +23.ii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-2986, DHJPAR0026567; same data as for preceding except: + +23.ii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-2989, DHJPAR0026570; same data as for preceding except: + +23.ii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3004, DHJPAR0026585; same data as for preceding except: + +29.ii.2008 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-3009, DHJPAR0026590; same data as for preceding except: + +29.ii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3016, DHJPAR0026597; same data as for preceding except: + +29.ii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3024, DHJPAR0026605; same data as for preceding except: + +29.ii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3046, DHJPAR0026627; same data as for preceding except: + +06.iii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3060, DHJPAR0026641; same data as for preceding except: + +06.iii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3061, DHJPAR0026642; same data as for preceding except: + +06.iii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3075, DHJPAR0026656; same data as for preceding except: + +12.iii.2008 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-3092, DHJPAR0026673; same data as for preceding except: + +12.iii.2008 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-3097, DHJPAR0026678; same data as for preceding except: + +12.iii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3106, DHJPAR0026687; same data as for preceding except: + +12.iii.2008 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-3111, DHJPAR0026692; same data as for preceding except: + +12.iii.2008 + + +. • + +1 ( +1♀ +, 0 + +) (0 + +, 0 + +); 08-SRNP-3168, DHJPAR0026749; same data as for preceding except: + +24.iii.2008 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-3216, DHJPAR0026797; same data as for preceding except: + +24.iii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3223, DHJPAR0026804; same data as for preceding except: + +24.iii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3233, DHJPAR0026814; same data as for preceding except: + +30.iii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3248, DHJPAR0026829; same data as for preceding except: + +30.iii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3252, DHJPAR0026833; same data as for preceding except: + +30.iii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3305, DHJPAR0026886; same data as for preceding except: + +05.iv.2008 + + +. • + +1 (0 + +, 0 + +) ( +1♀ +, 0 + +); 08-SRNP-3313, DHJPAR0026894; same data as for preceding except: + +05.iv.2008 + + +. • + +1 ( +1♀ +, 0 + +) (0 + +, 0 + +); 08-SRNP-3316, DHJPAR0026897; same data as for preceding except: + +05.iv.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3334, DHJPAR0026915; same data as for preceding except: + +05.iv.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3413, DHJPAR0026994; same data as for preceding except: + +11.iv.2008 + + +. • + +1 (0 + +, 0 + +) ( +1♀ +, 0 + +); 08-SRNP-3441, DHJPAR0027022; same data as for preceding except: + +11.iv.2008 + + +. • + +1 (0 + +, 0 + +) ( +1♀ +, 0 + +); 08-SRNP-3445, DHJPAR0027026; same data as for preceding except: + +11.iv.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3474, DHJPAR0027055; same data as for preceding except: + +17.iv.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3476, DHJPAR0027057; same data as for preceding except: + +17.iv.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3481, DHJPAR0027062; same data as for preceding except: + +17.iv.2008 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-3538, DHJPAR0027119; same data as for preceding except: + +23.iv.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3545, DHJPAR0027126; same data as for preceding except: + +23.iv.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3563, DHJPAR0027144; same data as for preceding except: + +23.iv.2008 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-3578, DHJPAR0027159; same data as for preceding except: + +23.iv.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3580, DHJPAR0027161; same data as for preceding except: + +23.iv.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3586, DHJPAR0027167; same data as for preceding except: + +23.iv.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3603, DHJPAR0027184; same data as for preceding except: + +23.iv.2008 + + +. • + +1 (0 + +, 0 + +) ( +1♀ +, 0 + +); 08-SRNP-3613, DHJPAR0027194; same data as for preceding except: + +23.iv.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3615, DHJPAR0027196; same data as for preceding except: + +23.iv.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3629, DHJPAR0027210; same data as for preceding except: + +23.iv.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3652, DHJPAR0027233; same data as for preceding except: + +30.iv.2008 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-3707, DHJPAR0027288; same data as for preceding except: + +06.v.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3710, DHJPAR0027291; same data as for preceding except: + +06.v.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3737, DHJPAR0027318; same data as for preceding except: + +06.v.2008 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-3762, DHJPAR0027343; same data as for preceding except: + +06.v.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3769, DHJPAR0027350; same data as for preceding except: + +12.v.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3797, DHJPAR0027378; same data as for preceding except: + +12.v.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3803, DHJPAR0027384; same data as for preceding except: + +12.v.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3832, DHJPAR0027413; same data as for preceding except: + +18.v.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3833, DHJPAR0027414; same data as for preceding except: + +18.v.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3857, DHJPAR0027438; same data as for preceding except: + +18.v.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3877, DHJPAR0027458; same data as for preceding except: + +18.v.2008 + + +. + + + +Area +de +Conservacion +Guanacaste + +, +Alajuela +, + +Sector + +San +Cristobal + + +, + +Potrero + +Argentina +: • 1 (0 + +, +1♂ +) (0 + +, 0 + +); 07-SRNP-67027, DHJPAR0025565; pastures; +Malaise +; + +520 m + +; +10.89021 +, +-85.38803 +; + +04.vii.2007 + +; +DH Janzen +& +W Hallwachs +leg. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-67059, DHJPAR0025597; same data as for preceding except: + +21.viii.2007 + +. • 1 (0 + +, +1♂ +) (0 + +, 0 + +); 07-SRNP-67069, DHJPAR0025607; same data as for preceding except: + +02.x.2007 + +. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-67112, DHJPAR0025650; same data as for preceding except: + +10.vi.2007 + +. • 1 (0 + +, +1♂ +) (0 + +, 0 + +), 07-SRNP-67146, DHJPAR0025684; same data as for preceding except: + +16.vii.2007 + +. • 1 ( +1♀ +, 0 + +) (0 + +, 0 + +); 07-SRNP-67200, DHJPAR0025738; same data as for preceding except: + +04.vii.2007 + +. • 1 (0 + +, +1♂ +) (0 + +, 0 + +); 07-SRNP-67214, DHJPAR0025752; same data as for preceding except: + +16.vi.2007 + +. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-67221, DHJPAR0025759; same data as for preceding except: + +16.vi.2007 + +. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-67224, DHJPAR0025762; same data as for preceding except: + +16.vi.2007 + +. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-67225, DHJPAR0025763; same data as for preceding except: + +16.vi.2007 + +. • 1 ( +1♀ +, 0 + +) (0 + +, 0 + +); 07-SRNP-67228, DHJPAR0025766; same data as for preceding except: + +16.vi.2007 + +. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-67255, DHJPAR0025793; same data as for preceding except: + +10.vi.2007 + +. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-67259, DHJPAR0025797; same data as for preceding except: + +22.vi.2007 + +. • 1 (0 + +, +1♂ +) (0 + +, 0 + +); 07-SRNP-67749, DHJPAR0027487; same data as for preceding except: + +03.viii.2007 + +. • 1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-3903, DHJPAR0027557; same data as for preceding except: + +11.ii.2008 + +. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3914, DHJPAR0027568; same data as for preceding except: + +17.ii.2008 + +. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3915, DHJPAR0027569; same data as for preceding except: + +17.ii.2008 + +. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3916, DHJPAR0027570; same data as for preceding except: + +17.ii.2008 + +. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3917, DHJPAR0027571; same data as for preceding except: + +23.ii.2008 + +. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3920, DHJPAR0027574; same data as for preceding except: + +23.ii.2008 + +. • 1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-3921, DHJPAR0027575; same data as for preceding except: + +23.ii.2008 + +. • 1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-3922, DHJPAR0027576; same data as for preceding except: + +23.ii.2008 + +. • 1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-3932, DHJPAR0027586; same data as for preceding except: + +06.iii.2008 + +. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-3933, DHJPAR0027587; same data as for preceding except: + +06.iii.2008 + + + +. + + + +Area +de +Conservacion +Guanacaste + +, +Alajuela +, + +Sector +Rincon +Rain Forest + +, + +Vado +Rio + +Francia +: • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66861, DHJPAR0025399; +Malaise +; + +400 m + +; +10.90093 +, +-85.28915 +; + +11.vi.2007 + +; +DH Janzen +& +W Hallwachs +leg. + + +• + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 07-SRNP-66864, DHJPAR0025402; same data as for preceding. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66866, DHJPAR0025404; same data as for preceding. • 1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66895, DHJPAR0025433; same data as for preceding except: + +21.ix.2007 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66922, DHJPAR0025460; same data as for preceding except: + +20.xi.2007 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66925, DHJPAR0025463; same data as for preceding except: + +20.xi.2007 + + +. • + +1 ( +1♀ +, 0 + +) (0 + +, 0 + +); 07-SRNP-66974, DHJPAR0025512; same data as for preceding except: + +29.vi.2007 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66977, DHJPAR0025515; same data as for preceding except: + +29.vi.2007 + + +. • + +1 ( +1♀ +, 0 + +) (0 + +, 0 + +); 07-SRNP-66978, DHJPAR0025516; same data as for preceding except: + +29.vi.2007 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-66981, DHJPAR0025519; same data as for preceding except: + +29.vi.2007 + + +. • + +1 ( +1♀ +, 0 + +) (0 + +, 0 + +); 07-SRNP-66996, DHJPAR0025534; same data as for preceding except: + +29.vi.2007 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 07-SRNP-67009, DHJPAR0025547; same data as for preceding except: + +05.vii.2007 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 07-SRNP-67572, DHJPAR0026102; same data as for preceding except: + +04.viii.2007 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 07-SRNP-67574, DHJPAR0026104; same data as for preceding except: + +27.x.2007 + + +. • + +1 ( +1♀ +, 0 + +) (0 + +, 0 + +); 08-SRNP-41728, DHJPAR0026171; same data as for preceding except: + +18.ii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-41729, DHJPAR0026172; same data as for preceding except: + +18.ii.2008 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-41739, DHJPAR0026182; same data as for preceding except: + +01.iii.2008 + + +. • + +1 (0 + +, 0 + +) (0 + +, +1♂ +); 08-SRNP-41741, DHJPAR0026184; same data as for preceding except: + +01.iii.2008 + + +. • + +1 (0 + +, +1♂ +) (0 + +, 0 + +); 08-SRNP-41787, DHJPAR0026230; same data as for preceding except: + +31.iii.2008 + + +. + + + +Diagnosis. + +Medioposterior band of scutellum mostly overlapping the medioanterior pit of metanotum ( +Figs 199F +, +220F +), pronotum with a distinct dorsal furrow ( +Figs 199C, I +, +200H +), petiole on T1 evenly narrowing distally, finely sculptured only laterally ( +Figs 199G, H +, +200G +), antenna longer than body, distal antennal flagellomere longer than penultimate, precoxal groove deep, smooth, and shiny ( +Figs 199A, I +, +200A, H +), fore wing with vein 1 cu-a curved, r vein curved ( +Fig. 200I +), dorsal outer depression on hind coxa present ( +Figs 199A, J +, +200A, J +), inner margin of eyes diverging slightly at antennal sockets ( +Figs 199B +, +200B +), and lateral grooves delimiting the median area on T2 clearly defined and reaching the distal edge of T2 ( +Figs 199G, H +, +200G +). + + + +Figure 199. + +Glyptapanteles scottshawi + +sp. nov. female 07-SRNP-66369 DHJPAR0024907, 08-SRNP-2950 DHJPAR0026531 +A +Habitus +B, D +Head +B +Frontal view +D +Dorsal view +C +Head, pronotum, propleuron, lateral view +E +Mesonotum, dorsal view +F +Scutellum, metanotum, propodeum, dorsal view +G +T1-3, dorsal view +H, J +Metasoma +H +Dorsal view +J +Lateral view +I +Mesosoma, lateral view. + + + + +Figure 200. + +Glyptapanteles scottshawi + +sp. nov. male 07-SRNP-67749 DHJPAR0027487, 08-SRNP-3917 DHJPAR0027571 +A +Habitus +B, D +Head +B +Frontal view +D +Dorsal view +C +Head, pronotum, propleuron, lateral view +E, J +Metasoma +E +Dorsal view +J +Lateral view +F +Scutellum, metanotum, propodeum, dorsal view +G +T1-3, dorsal view +H +Mesosoma, lateral view +I +Fore and hind wings. + + + + +Coloration + +( + +Fig. 199 +A-J + +). General body coloration black except scape proximally yellow-brown/reddish and distally brown; pedicel distally yellow-brown/reddish and proximally brown; first seven-eight proximal antennal flagellomeres completely yellow (the yellow coloration is darker on the first four antennal flagellomeres), remaining flagellomeres completely brown; tegulae yellow; labrum, mandible, propleuron distally, and dorsal furrow of pronotum yellow-brown/reddish; glossa, maxillary and labial palps pale yellow/ivory. Eyes and ocelli silver. Fore and middle legs dark yellow, except coxae and trochanters pale yellow/ivory; hind legs dark yellow except proximal half of coxae black, femora distally and tibiae brown, and tarsomeres dark yellow. Petiole on T1 with two colorations: proximal 1/4 yellow-brown/reddish and distal 3/4 brown, contours darkened and sublateral areas ivory/pale yellow; T2 with median and adjacent areas brown, and lateral ends ivory/pale yellow; T3 medially brown, proximally dark area coinciding with the width of dark area of median and adjacent areas on T2, but distally T3 narrowing, remaining area ivory/pale yellow; T4 and beyond completely brown; distally each tergum with a narrow ivory/pale yellow transparent band. In lateral view, T1-3 ivory/pale yellow; T4 and beyond brown. S1-5 ivory/yellow; hypopygium brown. + + + +Description. + +Head +( + +Fig. 199 +A-D + +). Head rounded with pubescence long and dense. Proximal three antennal flagellomeres longer than wide (0.25:0.08, 0.24:0.08, 0.24:0.08), distal antennal flagellomere longer than penultimate (0.14:0.06, 0.11:0.07), antenna longer than body (3.23, 2.48); antennal scrobes-frons shallow. Face flat or nearly so, with dense fine punctations, interspaces smooth and longitudinal median carina present. Frons smooth. Temple wide, punctate and interspaces wavy. Inner margin of eyes diverging slightly at antennal sockets; in lateral view, eye anteriorly convex and posteriorly straight. POL shorter than OOL (0.08, 0.12). Malar suture present. Median area between lateral ocelli slightly depressed. Vertex laterally pointed or nearly so and dorsally wide. + + +Mesosoma +( +Fig. 199A, E, F, I +). Mesosoma dorsoventrally convex. Mesoscutum proximally convex and distally flat, punctation distinct throughout, interspaces smooth. Scutellum triangular, apex sloped and fused with +BS +, scutellar punctation scattered throughout, in profile scutellum flat and on same plane as mesoscutum, phragma of the scutellum partially exposed; +BS +mostly overlapping the +MPM +; +ATS +demilune with complete undulate/reticulate carinae; dorsal +ATS +groove with semicircular/parallel carinae. Transscutal articulation with small and heterogeneous foveae, area just behind transscutal articulation nearly at the same level as mesoscutum (flat) and with same kind of sculpture as mesoscutum. Metanotum with +BM +upward; +MPM +semicircular and bisected by a median longitudinal carina; +AFM +with a small lobe and not as well delineated as +PFM +; +PFM +thick, smooth and with lateral ends rounded; ATM with undulate carinae throughout. Propodeum without median longitudinal carina, proximal half curved with medium-sized sculpture and distal half rugose; distal edge of propodeum with a flange at each side and without stubs; propodeal spiracle distally framed by a short concave carina; nucha surrounded by very short radiating carinae. Pronotum with a distinct dorsal furrow, dorsally with a well-defined smooth band; central area of pronotum and dorsal furrow smooth, but ventral furrow with short parallel carinae. Propleuron with fine rugae and dorsally without a carina. Metasternum convex. Contour of mesopleuron convex; precoxal groove deep, smooth and shiny; epicnemial ridge convex, teardrop-shaped. + + +Legs. +Ventral margin of fore telotarsus entire without seta, fore telotarsus proximally narrow and distally wide, and longer than fourth tarsomere (0.11, 0.07). Hind coxa with punctation only on ventral surface, dorsal outer depression present. Inner spur of hind tibia longer than outer spur (0.26, 0.20), entire surface of hind tibia with dense strong spines clearly differentiated by color and length. Hind telotarsus as equal in length as fourth tarsomere (0.12, 0.11). + + +Wings +( +Fig. 200I +). Fore wing with r vein slightly curved; 2RS vein straight; r and 2RS veins forming a weak, even curve at their junction and outer side of junction not forming a stub; 2M vein slightly curved/swollen; distally fore wing [where spectral veins are] with microtrichiae more densely concentrated than the rest of the wing; anal cell 1/3 proximally lacking microtrichiae; subbasal cell with a small smooth area, vein 2CUa absent and vein 2CUb spectral; vein 2 cu-a absent; vein 2-1A proximally tubular and distally spectral, although sometimes difficult to see; tubular vein 1 cu-a curved and complete, but junction with 1-1A vein spectral. Hind wing with vannal lobe very narrow, subdistally and subproximally straightened, and setae evenly scattered in the margin. + + +Metasoma +( +Fig. 199A, G, H, J +). Metasoma laterally compressed. Petiole on T1 finely sculptured only laterally, evenly narrowing distally (length 0.34, maximum width 0.17, minimum width 0.07) and with scattered pubescence concentrated in the first distal third. Lateral grooves delimiting the median area on T2 clearly defined and reaching the distal edge of T2 (length median area 0.14, length T2 0.14), edges of median area polished and lateral grooves deep, median area broader than long (length 0.14, maximum width 0.20, minimum width 0.05); T2 with scattered pubescence only distally. T3 longer than T2 (0.19, 0.14) and with scattered pubescence throughout. Pubescence on hypopygium dense. + + +Cocoons. +Unknown. + + + +Comments. +In some females, the propleuron distally yellow; both the dorsal and the ventral furrows of pronotum, the area of the mesoscutum just above the dorsal furrow of pronotum and the epicnemial ridge are lighter than mesosoma coloration (light brown, reddish or yellow-brown); proximal half of the petiole yellow-brown/reddish and distal half brown; the shape of dark area on T3 can be slightly different. In other specimens, the coloration of hind legs is yellow-brown instead of dark yellow. In other females, the penultimate sternum with two colorations: proximal half yellow and distal half brown. + + +Male + +( + +Fig. 200 +A-J + +). All the antennal flagellomeres have the same color; in some preserved males, the eyes are black and the ocelli reddish; in other preserved males, the coloration on metosoma varies thus: the petiole and the T3 are brown; the S3-4 are yellow, but with some brown tints, the S5 and beyond are completely brown; in other males, the hind legs are light yellow-brown. + + + +Etymology. + +Scott R. Shaw is a Professor and Insect Museum Curator at the University of +Wyoming +, Laramie, +WY +, +USA +. His research is focused in systematics of +Braconidae +, mainly +Meteorinae +, +Rogadinae +, and +Euphorinae +. + + + +Distribution. + +The adult parasitoids were collected in +Costa Rica +, ACG, Sector +Rincon +Rain Forest (Vado +Rio +Francia +) and Sector + +San +Cristobal + +( +Estacion +San Gerardo, Potrero +Argentina +, and +Rio +Blanco Abajo), during +June-November +2007 and +January-May +2008 at +400 m +, +520 m +, +550 m +, and +575 m +in pasture and rain forest. + + + +Biology. +Unknown. + + +Host. +Unknown. + + + \ No newline at end of file diff --git a/data/38/EF/1E/38EF1E636B9C0F8538534DB63889415D.xml b/data/38/EF/1E/38EF1E636B9C0F8538534DB63889415D.xml new file mode 100644 index 00000000000..069aa257c38 --- /dev/null +++ b/data/38/EF/1E/38EF1E636B9C0F8538534DB63889415D.xml @@ -0,0 +1,76 @@ + + + +A key to Grouvellinus Champion, 1923 from mainland China with descriptions of two new species (Coleoptera, Elmidae) + + + +Author + +Bian, Dongju + + + +Author + +Sun, Haibin + +text + + +ZooKeys + + +2016 + +623 + + +89 +104 + + + + +http://dx.doi.org/10.3897/zookeys.623.9610 + +journal article +http://dx.doi.org/10.3897/zookeys.623.9610 +1313-2970-623-89 +1E2C7E9156884560A69434A58213C2FA + + + +Taxon classification Animalia Coleoptera Elmidae + + + + +Grouvellinus tibetanus +Jaech +, 1984 + +Figures 19-20 + + + + +Grouvellinus tibetanus +Jaech +, 1984: 114. TL: Nepal. + + + +Distribution. +China: Xizang; Nepal. + + +Material examined. + +Paratype: 1 male: "Nepal, 1.3.81. / Tibetan. Gregze /leg. M. A. +Jaech +, N 31/ Tatopani" (white label); "Para / TYPUS" (red label). + + + + \ No newline at end of file diff --git a/data/38/EF/45/38EF456F0918702374D00F0ED0560A7B.xml b/data/38/EF/45/38EF456F0918702374D00F0ED0560A7B.xml new file mode 100644 index 00000000000..c13fb92257d --- /dev/null +++ b/data/38/EF/45/38EF456F0918702374D00F0ED0560A7B.xml @@ -0,0 +1,60 @@ + + + +New substitute name for the genus Poliocoris Slater, 1994 (Hemiptera, Heteroptera, Rhyparochromidae) + + + +Author + +Zhang, Dao-Wei + + + +Author + +Chen, Jing + +text + + +ZooKeys + + +2015 + +478 + + +147 +148 + + + + +http://dx.doi.org/10.3897/zookeys.478.9063 + +journal article +http://dx.doi.org/10.3897/zookeys.478.9063 +1313-2970-478-147 +40A80A097C504C47A360D1DFA3DA0599 + + + +Taxon classification Animalia Hemiptera Rhyparochromidae + + + +Neopoliocoris umbrosus (Slater, 1994) +comb. n. + + + + +Poliocoris umbrosus +Slater 1994 +: 120. + + + + \ No newline at end of file diff --git a/data/38/EF/48/38EF48CC54A458EA90274A2422E83CEB.xml b/data/38/EF/48/38EF48CC54A458EA90274A2422E83CEB.xml new file mode 100644 index 00000000000..e7708d19363 --- /dev/null +++ b/data/38/EF/48/38EF48CC54A458EA90274A2422E83CEB.xml @@ -0,0 +1,85 @@ + + + +Distribution patterns of Chinese Cixiidae (Hemiptera, Fulgoroidea), highlight their high endemic diversity + + + +Author + +Luo, Yang +Key Laboratory of Plant Protection Resources and Pest Management, Ministry of Education, Entomological Museum, College of Plant Protection, Northwest A & F University, Yangling, Shaanxi 712100, China, Yangling, China + + + +Author + +Bourgoin, Thierry +https://orcid.org/0000-0001-9277-2478 +Institut de Systematique, Evolution, Biodiversite, ISYEB-UMR 7205, MNHN-CNRS-Sorbonne Universite-EPHE-Univ. Antilles, Museum national d'Histoire naturelle, CP 50, 57 rue Cuvier, F- 75005, Paris, France +thierry.bourgoin@mnhn.fr + + + +Author + +Zhang, Jia-Lin +Key Laboratory of Plant Protection Resources and Pest Management, Ministry of Education, Entomological Museum, College of Plant Protection, Northwest A & F University, Yangling, Shaanxi 712100, China, Yangling, China + + + +Author + +Feng, Ji-Nian +Key Laboratory of Plant Protection Resources and Pest Management, Ministry of Education, Entomological Museum, College of Plant Protection, Northwest A & F University, Yangling, Shaanxi 712100, China, Yangling, China +jinianf@nwsuaf.edu.cn + +text + + +Biodiversity Data Journal + + +2022 + +2022-01-24 + + +10 + + +75303 +75303 + + + + +http://dx.doi.org/10.3897/BDJ.10.e75303 + +journal article +http://dx.doi.org/10.3897/BDJ.10.e75303 +1314-2828-10-e75303 +07802C19F192544C9F561556F25CA5C4 + + + + +Cixius cyclus Tsaur & Hsu, 1991 + + + + +Cixius cyclus +Tsaur & Hsu in Tsaur et al., 1991b: 256. + + + +Distribution + +China: Taiwan ( +Tsaur et al. 1991b +). + + + + \ No newline at end of file diff --git a/data/38/EF/4E/38EF4E901D736DD5587DD6E3FFC079A2.xml b/data/38/EF/4E/38EF4E901D736DD5587DD6E3FFC079A2.xml new file mode 100644 index 00000000000..e2140a687c5 --- /dev/null +++ b/data/38/EF/4E/38EF4E901D736DD5587DD6E3FFC079A2.xml @@ -0,0 +1,360 @@ + + + +An illustrated atlas of the vertebral morphology of extant non-caenophidian snakes, with special emphasis on the cloacal and caudal portions of the column + + + +Author + +Szyndlar, Zbigniew +Institute of Systematics and Evolution of Animals, Polish Academy of Sciences, Slawkowska 17, 31 - 016 Krakow, Poland + + + +Author + +Georgalis, Georgios L. +https://orcid.org/0000-0001-7759-6146 +Institute of Systematics and Evolution of Animals, Polish Academy of Sciences, Slawkowska 17, 31 - 016 Krakow, Poland +dimetrodon82@gmail.com + +text + + +Vertebrate Zoology + + +2023 + +2023-09-27 + + +73 + + +717 +886 + + + + +http://dx.doi.org/10.3897/vz.73.e101372 + +journal article +http://dx.doi.org/10.3897/vz.73.e101372 +2625-8498-73-717 +8F3D5EDA2F184E5CA53E2F7741FF1339 +318B657A15AB5708B3C35FC1A82B4945 + + + + +Aniliidae Stejneger, 1907 + + + +General information. + +The taxonomic content and exact affinities of the group that is commonly known as +"pipesnakes" +, i.e., the American + +Anilius + +Oken, 1816, and the Asian + +Anomochilus + +Berg, 1901, and + +Cylindrophis + +Wagler, 1828, has been variously altered throughout decades of systematic studies of snakes. They were once known during the 19th century under the names +Ilysiidae +(or Ilysioidea) (e.g., +Fitzinger 1826 +; +Bonaparte 1852 +; +Boulenger 1890b +, +1893 +; +Cope 1894 +, +1898 +; +Gadow 1901 +; +Janensch 1906 +) or +Tortricidae +(or +Tortricina +or Tortriciens) (e.g., + +Mueller +1831 + +; + +Dumeril +and Bibron 1844 + +; +Jan 1857 +, +1862 +, +1863 +; +Peters 1861 +; +Cope 1864 +, +1887 +, +1893 +, +1895 +, +1898 +; + +Guenther +1864 + +; +Jan 1865 +; +Carus 1868 +; + +Mueller +1880 + +; +Rochebrune 1884 +; +Zittel 1887-1890 +; + +Palacky +1898 + +). +Cope (1887) +also included the uropeltids in anilioids, while +Romer (1956) +, +Kuhn (1961) +, +Smith et al. (1977) +, and +McDowell (1975 +, +1987 +) further added + +Xenopeltis + +Reinwardt in +Boie +, 1827, and + +Loxocemus + +Cope, 1861. + +Guibe +(1970) + +placed in +Aniliidae +only + +Anilius + +, + +Cylindrophis + +, and + +Anomochilus + +. In a similar manner, +Anilioidea +was later confined to include these three genera, all pertaining to their own families or subfamilies (e.g., +Cundall et al. 1993 +). That traditional concept of +Anilioidea +was considered as a paraphyletic assemblage by +Gower et al. (2005) +, a view that has been subsequently followed by others ( +Smith 2013 +; +Head 2021 +; +Smith and Georgalis 2022 +). Indeed, recent molecular studies treat + +Anilius + +as the sister group of +Tropidophiidae +, united in a group termed +Amerophidia +, whereas + +Uropeltis + +Cuvier, 1829, and + +Cylindrophis + +are united in a more distantly related group termed +Uropeltoidea +(e.g., +Miralles et al. 2018 +; +Burbrink et al. 2020 +; +Zaher et al. 2023 +; see the respective entry below). As such, +Aniliidae +is currently conceived to include among extant snakes solely + +Anilius + +and its single species, + +Anilius scytale + +(Linnaeus, 1758), distributed only in northern South America. Fossorial habits for these snakes are already clearly indicated by their etymology, i.e., from the Greek +"ἀν-" +(privative affix for +"no" +, +"without" +) and +"ἥλιος" +( +"sun" +). + + +Although a number of fossil remains and taxa has been referred to aniliids in the past few decades (e.g., +Rage 1974 +, +1984 +, +1998 +; +Szyndlar 1994 +, +2009 +; + +Szyndlar and +Alferez +2005 + +; + +Auge +and Rage 2006 + +; +Syromyatnikova et al. 2019 +), taking also into consideration the paraphyly of the traditional concept of " +Anilioidea +", it is not possible to determine where exactly most of these lie within +Alethinophidia +(see +Head 2021 +; +Smith and Georgalis 2022 +). Accordingly, the sole few definite fossil occurrences of +Aniliidae +are known from the Late Cretaceous and Cenozoic of the Americas ( +Head 2021 +; +Head et al. 2022 +; +Smith and Georgalis 2022 +), including also the only known fossil record of the extant + +Anilius scytale + +, from the Pliocene of Venezuela ( + +Carrillo-Briceno +et al. 2021 + +). + + +Vertebral morphology of +Aniliidae +is characterized by being relatively heavily built, an elongate centrum, depressed cotyle and condyle, depressed neural arch, neural spine with short anterior lamina that is strongly reduced dorsoventrally but crosses most of the anteroposterior length of the neural arch, shallow (but not absent) median notch of the neural arch, elongate prezygapophyses elevated to just shorter than zygosphene and angled at around 20°-25°, prominent (very thick and plate-like in shape) hypapophysis in anterior trunk vertebrae and a distinct haemal keel in succeeding trunk vertebrae, lack of haemapophyses or hypapophyses in caudal vertebrae, and a very low number of caudal vertebrae (for more details see Description and figures of + +Anilius + +below). + + +Previous figures of vertebrae of extant +Aniliidae +have been so far presented by +Rochebrune (1881) +, +Hoffstetter and Gasc (1969) +, +Gasc (1974) +, +Hoffstetter and Rage (1977) +, +Dowling and Duellman (1978) +, +Rieppel (1979) +, +Ikeda (2007) +, +Palci et al. (2013a +, +2018 +), +Garberoglio et al. (2019) +, +Fachini et al. (2020) +, +Head (2021) +, and +Alfonso-Rojas et al. (2023) +. Among these, vertebrae from the cloacal and/or caudal series have only been figured so far by +Gasc (1974) +and +Alfonso-Rojas et al. (2023) +. Documentation of the embryonic development of aniliid vertebrae was provided by +Guerra-Fuentes et al. (2023) +. Quantitative studies on the intracolumnar variability of aniliid vertebrae have been conducted by +Gasc (1974) +and +Head (2021) +. Besides, important observations on the vertebrae of + +Anilius + +were made by +Smith (2013) +, while +Head (2021) +recently provided a comprehensive study of the vertebral morphology of +Aniliidae +coupled with an emended diagnosis for the family, recognizing diagnostic features on the vertebrae that could differentiate them from uropeltoids. + + + + \ No newline at end of file diff --git a/data/38/F0/06/38F0069FA0FE542C9F4015B5339F2B44.xml b/data/38/F0/06/38F0069FA0FE542C9F4015B5339F2B44.xml new file mode 100644 index 00000000000..b4b79218661 --- /dev/null +++ b/data/38/F0/06/38F0069FA0FE542C9F4015B5339F2B44.xml @@ -0,0 +1,332 @@ + + + +Five times over: 42 new Angustopila species highlight Southeast Asia's rich biodiversity (Gastropoda, Stylommatophora, Hypselostomatidae) + + + +Author + +Pall-Gergely, Barna +https://orcid.org/0000-0002-6167-7221 +Centre for Agricultural Research, Plant Protection Institute, Eoetvoes Lorand Research Network, Herman Otto ut 15, H- 1022 Budapest, Hungary +pallgergely2@gmail.com + + + +Author + +Hunyadi, Andras +Adria setany 10 G 2 / 5., H- 1148 Budapest, Hungary + + + +Author + +Vermeulen, Jaap J. +JK Art and Science, Lauwerbes 8, 2318 AT Leiden, Netherlands + + + +Author + +Grego, Jozef +Horna Micina 219, SK- 97401 Banska Bystrica, Slovakia + + + +Author + +Sutcharit, Chirasak +Animal Systematic Research Unit, Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand + + + +Author + +Reischuetz, Alexander +Puechhaimgasse 52, A- 3580 Horn, Austria + + + +Author + +Dumrongrojwattana, Pongrat +Department of Biology, Faculty of Science, Burapha University, 169 Longhardbangsaen Road, Muang District, Chonburi, 20131, Thailand + + + +Author + +Botta-Dukat, Zoltan +Centre for Ecological Research, Institute of Ecology and Botany, Alkotmany 2 - 4, H- 2600, Vacratot, Hungary + + + +Author + +Oerstan, Aydin +12501 Milestone Manor Lane, Germantown, Maryland, 20876, USA + + + +Author + +Fekete, Judit +University of Pannonia, Centre of Natural Science, Research Group of Limnology, Egyetem u. 10, H- 8200 Veszprem, Hungary & Centre for Ecological Research, Institute of Aquatic Ecology, Department of Tisza Research, 18 / c Bem square, H- 4026 Debrecen, Hungary + + + +Author + +Jochum, Adrienne +https://orcid.org/0000-0002-6624-6412 +Naturhistorisches Museum der Burgergemeinde Bern, CH- 3005 Bern, Switzerland & Institute of Ecology and Evolution, University of Bern, CH- 3012 Bern, Switzerland & Senckenberg Forschungsinstitut und Naturmuseum, 60325 Frankfurt am Main, Germany + +text + + +ZooKeys + + +2023 + +2023-02-13 + + +1147 + + +1 +177 + + + + +http://dx.doi.org/10.3897/zookeys.1147.93824 + +journal article +http://dx.doi.org/10.3897/zookeys.1147.93824 +1313-2970-1147-1 +9BB9881B0076473D8E53155D37CA1F50 +FF2B6B317B505F9EA0E1000BDCD16CE7 + + + + + +Angustopila cavicola +Pall-Gergely +& Dumrongrojwattana + +sp. nov. + + + + +Figs 30 +, 32 +, 33 + + + +Type material. + +Holotype +: Thailand • 1 empty shell (H: 1.18 mm, D: 0.92 mm); Loei Province, Phu Tham Pha Tang; approx. GPS coordinates: +17°56.91'N +, +101°55.35'E +; 29 Jun. 2016; P. Dumrongrojwattana, P. Juangsantad, K. Khwantong, N. Namisa & P. Panthong leg.; CUMZ 7441. + + +Paratypes +: Thailand • 2 figured shells, same data as for holotype; HNHM 100181 • 8 shells; same data as for holotype; coll. PD • 8 shells; same data as for holotype; coll. PGB • 2 specimens in ethanol; same data as for holotype; coll. PGB. + + + +Additional material. + + +Thailand +• 11 j/b shells; same data as for holotype; coll. PD + +. + +Laos +• 1 shell; +Udomxai Province +, +6.5 km +southeast from centre of +Na Mor +towards +Udomxai +, +Ban Nathong +, +Tham Nathong +, below cave spring (locality code: 2019/118); +20°52.37'N +, +101°46.98'E +; + +635 m +a.s.l. + +; +7 Oct. 2019 +; +A. Hunyadi +leg.; coll. HA + +. + + + +Diagnosis. + +A medium-sized to large, conical + +Angustopila + +species with few whorls, a narrow umbilicus, a conspicuously large aperture, a strongly expanded peristome and a short but strong parietal tooth that points slightly towards the palatal wall. + + + +Description (of the type sample). + +Shell medium to large-sized for the genus, higher to much higher than wide; off-white, conical, apex broad, body whorl widest from apertural view; protoconch consists of 1.25 whorls, without spiral striation; teleoconch finely ornamented with irregular radial growth lines crossed by weak rows of irregularly spaced spiral threads (ca. 12-14 on body whorl from apertural view); sculpture weaker than in most other + +Angustopila + +species; whorls 3.5-4 (conspicuously few compared to large shell size), rounded; aperture slightly oblique to shell axis from lateral view; umbilicus very narrow; aperture subcircular, parietal callus convex; peristome strongly expanded especially at parietal and palatal region, not reflected; parietal callus overlapping and not smeared onto penultimate whorl; parietal tooth elevated, strong, normally long, slightly bent towards palatal side, does not reach parietal callus. + + + +Measurements (in mm). + +H = 1.02-1.18, D = 0.87-0.97, H/D*100 = 109.3-130.3 (shells from the type locality; +n += 6), RUD = 17.6-19.8 ( +n += 3); H = 1.27, D = 0.99, H/D*100 = 128.3, RUD = 20.2 (2019/118; +n += 1). + + + +Differential diagnosis. + + +Angustopila fabella + +is smaller, has a more pointed apex, a comparatively smaller aperture, a weaker sculpture, and a less expanded peristome. All other conical species with a single tooth are much smaller than + +A. cavicola + +sp. nov. + + + +Etymology. + +This new species was collected inside a cave, in the dark zone ( + +Angustopila cavicola + +means cave-dweller in Latin). + + + +Distribution. + +The type series is known from Loei Province, Thailand. An additional, single shell, reminiscent of the typical + +A. cavicola + +sp. nov. shells, was collected in Northern Laos ca. 325 km north of the type series (Fig. +31 +). + + + +Figure 30. + +Angustopila cavicola + +Pall-Gergely +& Dumrongrojwattana, sp. nov. (holotype, CUMZ 7441). Apertural ( +A +), ventral ( +B +), lateral ( +C +) and apical (D) sides of the shell; microstructure of the protoconch showing protoconch-teleoconch boundary ( +E +), eroded ventral ( +F +) and frontal ( +G +) surface of the body whorl. + + + + +Figure 31. +Distribution of + +Angustopila + +species. + + + + +Figure 32. +Variability of + +Angustopila cavicola + +Pall-Gergely +& Dumrongrojwattana, sp. nov. +A +holotype (CUMZ 7441) +B, C +paratypes (HNHM 100181). + + + + +Figure 33. + +Angustopila cavicola + +Pall-Gergely +& Dumrongrojwattana, sp. nov. from Laos (2019/118). Apertural ( +A +), ventral ( +B +), lateral ( +C +) and apical ( +D +) sides of the shell; aperture ( +E +), microstructure of the protoconch ( +F +), ventral ( +G +) and frontal ( +H +) surface of the body whorl. + + + + +Remarks. +The single shell from Laos has an even weaker sculpture (practically smooth) and a lower parietal tooth than the Thai ones. Otherwise, it is similar to the Thai population in terms of shell size, and shell and aperture shapes. + + + \ No newline at end of file diff --git a/data/38/F1/0B/38F10BEB56CC59A78250D08449C39B8E.xml b/data/38/F1/0B/38F10BEB56CC59A78250D08449C39B8E.xml new file mode 100644 index 00000000000..328f095939e --- /dev/null +++ b/data/38/F1/0B/38F10BEB56CC59A78250D08449C39B8E.xml @@ -0,0 +1,91 @@ + + + +An annotated checklist of the Crambidae of the region of Murcia (Spain) with new records, distribution and biological data (Lepidoptera: Pyraloidea, Crambidae) + + + +Author + +Garre, Manuel J. +Universidad de Murcia, Murcia, Spain + + + +Author + +Girdley, John +Universidad de Murcia, Murcia, Spain + + + +Author + +Guerrero, Juan J. +Universidad de Murcia, Murcia, Spain + + + +Author + +Rubio, Rosa M. +Universidad de Murcia, Murcia, Spain + + + +Author + +Ortiz, Antonio S. +https://orcid.org/0000-0002-3877-6096 +Universidad de Murcia, Murcia, Spain +aortiz@um.es + +text + + +Biodiversity Data Journal + + +2021 + +2021-08-03 + + +9 + + +69388 +69388 + + + + +http://dx.doi.org/10.3897/BDJ.9.e69388 + +journal article +http://dx.doi.org/10.3897/BDJ.9.e69388 +1314-2828-9-e69388 +65689D3026F55F7DA415A977389BD22F + + + + +Anania (Ametasia) murcialis (Ragonot, 1895) + + + +Distribution +Atlanto-Mediterranean + + +Notes + +References: +Ragonot (1895) +, +Agenjo (1962) +. Biological data: Bivoltine. Flight period: V-VI, IX. + + + + \ No newline at end of file diff --git a/data/38/F1/34/38F134F3969DB4C0AB8C888808F23FC8.xml b/data/38/F1/34/38F134F3969DB4C0AB8C888808F23FC8.xml new file mode 100644 index 00000000000..58e22498bd7 --- /dev/null +++ b/data/38/F1/34/38F134F3969DB4C0AB8C888808F23FC8.xml @@ -0,0 +1,110 @@ + + + +Order Chiroptera - Family Hipposideridae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1 + + + +365 +379 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316519 + + + + + +Hipposideros coronatus +Peters 1871 + + + + + + + +Hipposideros coronatus +Peters 1871 + +, +Monatsb. K. Preuss. Akad. Wiss. Berlin, 1871: 327 + +. + + + + +Type Locality: + +Philippines +, Mindanao, Surigao, Mainit. + + + + + +Vernacular Names: +Large Mindanao Leaf-nosed Bat +. + + + + +Distribution: +NE Mindanao ( +Philippines +). + + + + +Conservation: +IUCN +2003 and +IUCN +/ +SSC +Action Plan (2001) – Lower Risk (nt). + + + + +Discussion: + +bicolor + +species group. See +Ingle and Heaney (1992) +. + + + + \ No newline at end of file diff --git a/data/38/F1/5D/38F15DBCE948F2DEE8976C06C471D020.xml b/data/38/F1/5D/38F15DBCE948F2DEE8976C06C471D020.xml new file mode 100644 index 00000000000..a0d746d50bc --- /dev/null +++ b/data/38/F1/5D/38F15DBCE948F2DEE8976C06C471D020.xml @@ -0,0 +1,64 @@ + + + +List of primary types of the larentiine moth species (Lepidoptera: Geometridae) described from Indonesia - a starting point for biodiversity assessment of the subfamily in the region + + + +Author + +Schmidt, Olga + +text + + +Biodiversity Data Journal + + +2015 + +3 + + +5447 +5447 + + + + +http://dx.doi.org/10.3897/BDJ.3.e5447 + +journal article +http://dx.doi.org/10.3897/BDJ.3.e5447 +1314-2828--5447 + + + + +Sterrhochaeta (Sterrhochaeta) rectilineata indirecta Prout, 1958 + + + + +Sterrhochaeta (Sterrhochaeta) rectilineata indirecta +Prout 1958 + + + +Materials + + +Type status: +Holotype +. Occurrence: sex: +f +; Record Level: ownerInstitutionCode: NHM + + + + +Distribution +Type locality: Celebes (west) [Sulawesi], Paloe, Sidaonta, 4500 ft. + + + \ No newline at end of file diff --git a/data/38/F1/83/38F183C65609532920A7561401575164.xml b/data/38/F1/83/38F183C65609532920A7561401575164.xml new file mode 100644 index 00000000000..922984625fc --- /dev/null +++ b/data/38/F1/83/38F183C65609532920A7561401575164.xml @@ -0,0 +1,80 @@ + + + +Nine genera of Eucnemidae (Coleoptera) new to Peru, with a key to Peruvian genera + + + +Author + +Vahtera, Varpu + + + +Author + +Muona, Jyrki + + + +Author + +Linna, Ari + + + +Author + +Saeaeksjaervi, Ilari E. + +text + + +Biodiversity Data Journal + + +2015 + +3 + + +4493 +4493 + + + + +http://dx.doi.org/10.3897/BDJ.3.e4493 + +journal article +http://dx.doi.org/10.3897/BDJ.3.e4493 +1314-2828--4493 + + + + +Gagatellus Fleutiaux, 1912 + + + +Materials + + +Type status: +Other material +. Taxon: higherClassification: Coleoptera; Eucnemidae; Macraulacinae; Macraulacini; genus: Gagatellus Fleutiaux, 1912 + + + + +Notes + +The genus was not found in our study. Preiviously one species, +Gagatellus baeri +Fleutiaux, 1912, is reported from Peru ( +Schenkling 1928 +). + + + + \ No newline at end of file diff --git a/data/38/F1/AE/38F1AE7239279BF91EF4924BD992279A.xml b/data/38/F1/AE/38F1AE7239279BF91EF4924BD992279A.xml new file mode 100644 index 00000000000..44edb5ed55f --- /dev/null +++ b/data/38/F1/AE/38F1AE7239279BF91EF4924BD992279A.xml @@ -0,0 +1,70 @@ + + + +Species plantarum: exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas + + + +Author + +Linnaeus, Carolus + +text + +1753 +Laurentius Salvius + +Stockholm + + + +https://doi.org/10.5962/bhl.title.669 + +book +10.5281/zenodo.3931989 +3931989 + + + + +Stellaria biflora +, +spec. nov. + + + +7. Stellaria foliis subulatis, scapis subbifloris, petalis emarginatis, germinibus oblongis, calycibus striatis. + +Sagina ramis erectis bifloris. +Fl. lapp. 158. +* + + +Moehringia scapis bifloris. +Fl. suec. 316. + + +Arenaria foliis subulatis, calycibus striatis, germinibus oblongis, floribus corymbosis. +Amoen. acad.1. p.158. +* + + + + +Habitat in Alpibus +Lapponicis +. ♃ + + + + +Planta +parva, facie Saginae. +Folia +radicalia subulata, in 423 Dd4 acervum congesta. +Caules +digitales, filiformes, maxima parte nudi: superne bifidi in 2 pedunculos subjecto pari foliorum: altero pedunculo in medio foliolis duobus. + + + + \ No newline at end of file diff --git a/data/38/F2/FA/38F2FAE863D867A5D6BEB8044C1ABD79.xml b/data/38/F2/FA/38F2FAE863D867A5D6BEB8044C1ABD79.xml new file mode 100644 index 00000000000..1563ccf6d26 --- /dev/null +++ b/data/38/F2/FA/38F2FAE863D867A5D6BEB8044C1ABD79.xml @@ -0,0 +1,60 @@ + + + +Die Milbenfauna der Nordseeinsel Wangerooge + + + +Author + +Willmann, C. + +text + + +Veröffentlichungen des Instituts für Meeresforschung Bremerhaven + + +1952 + +1 + + +139 +186 + + + + +http://unknown + +journal article +ORI11037 +1CD7624C-FC8F-4DD0-AA34-762D8FFB6267 + + + + +92. +Hauptmannia brevicollis Oudemans +1910. + + + + + +Fundort: Altes +Anspuelicht +von Winterhochfluten, + +18. VI. 49 + +, mehrere Exemplare. + + + + +Diese Art ist nur als Larva bekannt. + + + \ No newline at end of file diff --git a/data/38/F3/44/38F3445DBA4659E5AA8689C84DAABE13.xml b/data/38/F3/44/38F3445DBA4659E5AA8689C84DAABE13.xml new file mode 100644 index 00000000000..d43c0d8faa7 --- /dev/null +++ b/data/38/F3/44/38F3445DBA4659E5AA8689C84DAABE13.xml @@ -0,0 +1,169 @@ + + + +Annotated checklist of freshwater molluscs from the largest freshwater lake in Southeast Asia + + + +Author + +Ng, Ting Hui +Lee Kong Chian Natural History Museum, Faculty of Science, National University of Singapore, 2 Conservatory Drive, 117377, Singapore +https://orcid.org/0000-0002-5123-0039 + + + +Author + +Jeratthitikul, Ekgachai +Animal Systematics and Molecular Ecology Laboratory, Department of Biology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand +https://orcid.org/0000-0002-3477-9548 + + + +Author + +Sutcharit, Chirasak +Animal Systematics Research Unit, Department of Biology, Faculty of Science, Chulalongkorn University, 254 Phayathai Road, Pathumwan, Bangkok 10330, Thailand + + + +Author + +Chhuoy, Samol +Inland Fisheries Research and Development Institute (IFReDI), Fisheries Administration, No. 86, Norodom Blvd., PO Box 582, Phnom Penh, Cambodia & Wonders of the Mekong Project, c / o IFReDI, No. 86, Norodom Blvd., PO Box 582, Phnom Penh, Cambodia + + + +Author + +Pin, Kakada +Wonders of the Mekong Project, c / o IFReDI, No. 86, Norodom Blvd., PO Box 582, Phnom Penh, Cambodia + + + +Author + +Pholyotha, Arthit +Animal Systematics Research Unit, Department of Biology, Faculty of Science, Chulalongkorn University, 254 Phayathai Road, Pathumwan, Bangkok 10330, Thailand +https://orcid.org/0000-0001-6677-1164 + + + +Author + +Siriwut, Warut +Animal Systematics and Molecular Ecology Laboratory, Department of Biology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand + + + +Author + +Srisonchai, Ruttapon +Department of Biology, Faculty of Science, Khon Kaen University, Khon Kaen 40002, Thailand + + + +Author + +Hogan, Zeb S. +Wonders of the Mekong Project, c / o IFReDI, No. 86, Norodom Blvd., PO Box 582, Phnom Penh, Cambodia & Department of Biology, University of Nevada, 1664 N. Virginia Street, Reno, NV 89557, USA + + + +Author + +Ngor, Peng Bun +Inland Fisheries Research and Development Institute (IFReDI), Fisheries Administration, No. 86, Norodom Blvd., PO Box 582, Phnom Penh, Cambodia & Wonders of the Mekong Project, c / o IFReDI, No. 86, Norodom Blvd., PO Box 582, Phnom Penh, Cambodia +https://orcid.org/0000-0002-3659-6577 +pengbun.ngor@gmail.com + +text + + +ZooKeys + + +2020 + +958 + + +107 +141 + + + + +http://dx.doi.org/10.3897/zookeys.958.53865 + +journal article +http://dx.doi.org/10.3897/zookeys.958.53865 +1313-2970-958-107 +AB196008154249D4B23E1892D2191C18 +377C3EF18E8951FD9599616E45E03C94 + + + + +Mekongia rattei (Crosse & Fischer, 1876) +Fig. 5G + + + + +Paludina rattei +Crocsse & Fischer, 1876: 317. Type locality: "Stung Chinit, Cambodia". + + +Mekongia rattei +: +Brandt 1974 +: 44-45, pl. 3, figs 51, 52. + + + +Material examined. +CIFI.MOL.042, MUMNH.VIV.001, MUMNH.VIV.002, MUMNH.VIV.003, ZRC.MOL.015744, ZRC.MOL.015745, ZRC.MOL.015743. + + +Distribution and habitat. +Tonle Sap Lake; Chi Kraeng River and Sreng River in Siem Reap Province; Phumi Phsar River in Kampong Chhnang Province (locality no. 7, 8, 11, 13, 16, 20, 24, 27, 36, 37 and 39). + + +Remarks. + + +Mekongia rattei + +is sold in local markets surrounding the Lake. This species along with + +Corbicula + +spp. are commercially harvested from the Lake to be sold locally and exported abroad for human consumption and as animal feed in local poultry farms (Fig. +4B +). Another record of + +Mekongia + +from the Tonle Sap basin and surrounding drainages is + +Mekongia swainsoni + +(see +Brandt 1974 +; +Ngor et al. 2018d +). + +Mekongia rattei + +differs from + +Mekongia swainsoni + +by its larger size and conic shape of spire. + + + + \ No newline at end of file diff --git a/data/38/F3/7A/38F37AF7BC0AAAE8E36EF2BC7F85D978.xml b/data/38/F3/7A/38F37AF7BC0AAAE8E36EF2BC7F85D978.xml new file mode 100644 index 00000000000..3eb5ceb212d --- /dev/null +++ b/data/38/F3/7A/38F37AF7BC0AAAE8E36EF2BC7F85D978.xml @@ -0,0 +1,74 @@ + + + +An annotated checklist of the chrysidid wasps (Hymenoptera, Chrysididae) from China + + + +Author + +Rosa, Paolo +Via Belvedere 8 / d, I- 20881 Bernareggio (MB), Italy + + + +Author + +Wei, Na-sen +Department of Entomology, College of Natural Resources and Environment, South China Agricultural University, Guangzhou 510640, China + + + +Author + +Xu, Zai-fu +Department of Entomology, College of Natural Resources and Environment, South China Agricultural University, Guangzhou 510640, China + +text + + +ZooKeys + + +2014 + +2014-11-19 + + +455 + + +1 +128 + + + + +http://dx.doi.org/10.3897/zookeys.455.6557 + +journal article +http://dx.doi.org/10.3897/zookeys.455.6557 +1313-2970-455-1 +7346B2B940BF4358AFE4B3F30023F9F2 +FF9EFF935938FF8EFF4DFFEBFFAEFF82 +578622 + + + + +66. +Omalus helanshanus Wei, Rosa, Liu & Xu, 2014 + + + + +Omalus helanshanus +Wei, Rosa, Liu & Xu, 2014: 39. Holotype ♀, China: Inner Mongolia, Helanshan, Gulaben (32 (key), 39 (type series: Inner Mongolia, Helanshan, Gulaben, Dayanggou; Shuimogou; Habeigou, Huangliangzi; Halawuchagou; Halawubeigou; Halawu, descr.), 40 (pl. 7), 41 (pl. 8A-8F), depository: SCAU)*. + + + +Distribution. +China (Inner Mongolia). + + + \ No newline at end of file diff --git a/data/38/F4/DC/38F4DCDE9880990C6DF80FB77C60E1D8.xml b/data/38/F4/DC/38F4DCDE9880990C6DF80FB77C60E1D8.xml new file mode 100644 index 00000000000..e3f6ee833fd --- /dev/null +++ b/data/38/F4/DC/38F4DCDE9880990C6DF80FB77C60E1D8.xml @@ -0,0 +1,168 @@ + + + +Synopsis of the pelidnotine scarabs (Coleoptera, Scarabaeidae, Rutelinae, Rutelini) and annotated catalog of the species and subspecies + + + +Author + +Moore, Matthew R. +Department of Entomology and Nematology, University of Florida Building 1881 Natural Drive Area, Steinmetz Hall, Box 110620, Gainesville, FL 32611 - 0620, USA + + + +Author + +Jameson, Mary L. +Department of Biological Sciences, Wichita State University 1845 Fairmount, Box 26, Wichita, KS 67260 - 0026, USA +maryliz.jameson@gmail.com + + + +Author + +Garner, Beulah H. +Natural History Museum, Insects Division, Department of Life Sciences, Cromwell Road, London SW 7 5 BD, UK + + + +Author + +Audibert, Cedric +Musee des Confluences, Centre de Conservation et d'Etude des Collections, 13 A Rue Bancel, F- 69007 Lyon, France + + + +Author + +Smith, Andrew B. T. +Research Division, Canadian Museum of Nature, P. O. Box 3443, Station D, Ottawa, Ontario, K 1 P 6 P 4, Canada + + + +Author + +Seidel, Matthias + +text + + +ZooKeys + + +2017 + +2017-04-06 + + +666 + + +1 +349 + + + + +http://dx.doi.org/10.3897/zookeys.666.9191 + +journal article +http://dx.doi.org/10.3897/zookeys.666.9191 +1313-2970-666-1 +B3C377E8BBB14F328AECA2C22D1E625A +C43EEB41A94B930FFE439D1FAD29FF9C +579453 + + + + +Homonyx santiagensis Ohaus, 1913 + + + + +Homonyx chalceus santiagensis +Ohaus, 1913: 494 [original combination]. + + +Homonyx santiagensis +Ohaus [new species status by +Soula 2010a +: 12]. + + + +Distribution. + +ARGENTINA: +Cordoba +, Jujuy, Santiago del Estero ( +Ohaus 1913 +, +1934b +, +Blackwelder 1944 +, +Machatschke 1972 +, +Krajcik 2008 +, +Soula 2010a +). + + + +Types. + +1 ♂ lectotype and 1 paralectotype at ZMHB (Fig. +32 +) ( +Soula 2010a +). + + + +Remarks. + +Krajcik (2012 +, +2013 +) considered + +H. santiagensis + +to be a subspecies of + +H. chalceus + +. + + + +Figure 32. + +Homonyx chalceus santiagensis + +Ohaus (valid name + +H. santiagensis + +) type male (see " +Type specimens and lectotype designation +" in Methods) from ZMHB. +A +Dorsal habitus +B +Lateral habitus +C +Specimens labels and male genitalia +D +Male genitalia, lateral view +E +Parameres, caudal view. + + + + + \ No newline at end of file diff --git a/data/38/F5/3C/38F53C8FFBD9C3C56B88CE01F5F276FC.xml b/data/38/F5/3C/38F53C8FFBD9C3C56B88CE01F5F276FC.xml new file mode 100644 index 00000000000..490540da940 --- /dev/null +++ b/data/38/F5/3C/38F53C8FFBD9C3C56B88CE01F5F276FC.xml @@ -0,0 +1,50 @@ + + + +Notes on Pauropoda (Myriapoda) from USA, with descriptions of two new species + + + +Author + +Scheller, Ulf + +text + + +ZooKeys + + +2011 + +115 + + +19 +26 + + + + +http://dx.doi.org/10.3897/zookeys.115.1190 + +journal article +http://dx.doi.org/10.3897/zookeys.115.1190 +1313-2970-115-19 + + + + +Eurypauropus spinosus Ryder, 1879 + + + +Material. + +USA, Indiana, Bloomington, 37 ad. (36♀, 1 sex?), 1?ad.(sex?), 2 subad. 8(♀), 2 stad.?(sex?), " +Eurypauropus +93 Bollm. Col.?". + + + + \ No newline at end of file diff --git a/data/38/F5/75/38F5755E57EAC490B813F7E004815527.xml b/data/38/F5/75/38F5755E57EAC490B813F7E004815527.xml new file mode 100644 index 00000000000..4fd6f03c59c --- /dev/null +++ b/data/38/F5/75/38F5755E57EAC490B813F7E004815527.xml @@ -0,0 +1,63 @@ + + + +Species plantarum: exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas + + + +Author + +Linnaeus, Carolus + +text + +1753 +Laurentius Salvius + +Stockholm + + + +https://doi.org/10.5962/bhl.title.669 + +book +10.5281/zenodo.3931989 +3931989 + + + + +Panicum latifolium +, +spec. nov. + + + +17. Panicum panicula racemis lateralibus simplicibus, foliis ovato-lanceolatis collo pilosis. + +Gramen +virginianum, lato brevique folio, panicula rariore. +Moris. hist.3. p.196. s.8. t.5. f.4. + + +Gramen miliaceum sylvaticum maximum, semine albo. +Sloan. jam. 34. hist.1. p.114. t.71. f.3. + + + + +Habitat in +America +. + + + + +Folia +latitudine Commelinae, ad fauces amplexicaulia; extus collo circum fauces villoso, etiam basi foliorum margine pilosa. Panicula valde mediocris ex racemis lateralibus, non subdivisis, sed pedicellos proprios, nec subdivisos proferentes. +Flores +mutici, majusculi. + + + + \ No newline at end of file diff --git a/data/38/F5/A1/38F5A1B13C2FEFBB58974E9F16E099E3.xml b/data/38/F5/A1/38F5A1B13C2FEFBB58974E9F16E099E3.xml new file mode 100644 index 00000000000..d7d46c0a48b --- /dev/null +++ b/data/38/F5/A1/38F5A1B13C2FEFBB58974E9F16E099E3.xml @@ -0,0 +1,60 @@ + + + +Species plantarum: exhibentes plantas rite cognitas, ad genera relatas, cum differentiis specificis, nominibus trivialibus, synonymis selectis, locis natalibus, secundum systema sexuale digestas + + + +Author + +Linnaeus, Carolus + +text + +1753 +Laurentius Salvius + +Stockholm + + + +https://doi.org/10.5962/bhl.title.669 + +book +10.5281/zenodo.3931989 +3931989 + + + + +Bulbocodium serotinum +, +spec. nov. + + + + +2. Bulbocodium foliis subulato-linearibus. +Roy. lugdb. 41. + + +Bulbocodium alpinum juncifolium, flore unico: intus albo extus squalide rubente. +Raj. angl.3. p.374. t.17. f.1. + + +Pseudo-Narcissus gramineo folio. +Bauh. pin. 51. prodr. 27. +Rudb. elys.2. p.64. f.9. + + + + +Habitat in Alpibus +Helvetiae +, +Angliae +. ♃ + + + + \ No newline at end of file diff --git a/data/38/F5/A8/38F5A8F6874A54318CE2364F665A840D.xml b/data/38/F5/A8/38F5A8F6874A54318CE2364F665A840D.xml new file mode 100644 index 00000000000..baec7714a3f --- /dev/null +++ b/data/38/F5/A8/38F5A8F6874A54318CE2364F665A840D.xml @@ -0,0 +1,103 @@ + + + +The Nazeris fauna of the Nanling Mountain Range, China (Coleoptera, Staphylinidae, Paederinae) + + + +Author + +Lin, Xiao-Bin +Department of Biology, College of Life Sciences, Shanghai Normal University, 100 Guilin Road, 1 st Educational Building 423 - A Room, Shanghai, 200234 China + + + +Author + +Hu, Jia-Yao +Department of Biology, College of Life Sciences, Shanghai Normal University, 100 Guilin Road, 1 st Educational Building 423 - A Room, Shanghai, 200234 China +hujiayaonazeris@gmail.com + +text + + +ZooKeys + + +2021 + +2021-09-08 + + +1059 + + +117 +133 + + + + +http://dx.doi.org/10.3897/zookeys.1059.72240 + +journal article +http://dx.doi.org/10.3897/zookeys.1059.72240 +1313-2970-1059-117 +74BFDC468DE9424CB1685F03CF818C3C +F28E541B35505760B314F23160885A35 + + + + +Nazeris yuyimingi Hu & Qiao, 2019 + + + + +Fig. 27 + + + +Non-type material examined. + +China: Guangxi Prov. +: +Xing'an +, +Mao'ershan +N. R.: 1 ♀, nr. Antangping, +25°54'44.07"N +, +110°27'37.68"E +, 1660 m, 7.v.2021, sifted, Yin, Zhang, Pan and Shen leg. (SNUC). + + + +Comparative notes. + + +Nazeris yuyimingi + +is similar in general appearance and aedeagal characters to + +N. chenyanae + +Hu & Li, 2017, but can be separated by the shallowly emarginate male sternite VII ( +Hu and Qiao 2019 +: 437, fig. 26), by the narrower ventral process and the wider apex of the dorso-lateral apophyses of the aedeagus in ventral view ( +Hu and Qiao 2019 +: 437, fig. 28). + + + +Distribution and habitat data. + +The species is known only from +Mao'ershan +in northeast Guangxi (Fig. +27 +). The specimen was collected by sifting leaf litter at altitudes of 1143-1660 m. + + + + \ No newline at end of file diff --git a/data/38/F7/3F/38F73F2C1B8132D454BDB0FA8161EB26.xml b/data/38/F7/3F/38F73F2C1B8132D454BDB0FA8161EB26.xml new file mode 100644 index 00000000000..96ce28fc466 --- /dev/null +++ b/data/38/F7/3F/38F73F2C1B8132D454BDB0FA8161EB26.xml @@ -0,0 +1,196 @@ + + + +Order Rodentia - Family Echimyidae + + + +Author + +Wilson, Don E. + + + +Author + +Reeder, DeeAnn + +text + + +2005 +The Johns Hopkins University Press + +Baltimore + + + +Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 2 + + + +1575 +1592 + + + +book chapter +0-8018-8221-4 +10.5281/zenodo.7316535 + + + + + +Thrichomys apereoides +(Lund 1839) + + + + + + + +[Nelomys] apereoides +Lund 1839 + +, +Afh. K. Danske Vid. Selsk.: 38 + +. + + + + +Type Locality: + +Brazil +, +Minas Gerais +, Lagoa Santa. + + + + + +Vernacular Names: +Common Punare +. + + + + +Subspecies: +: + + +Subspecies + +Thrichomys apereoides +subsp. +apereoides +Lund 1839 + + + +Subspecies + +Thrichomys apereoides +subsp. +laurenteus +Thomas 1904 + + + + + +Distribution: +S and SE +Brazil +. + + + + +Conservation: +IUCN +– Lower Risk (lc). Common. + + + + +Discussion: +Formerly referred to as + +Cercomys cunicularius + +, a composite ( + +Petter, 1973 +b + +; + +Mares et al., 1981 +a +:120 + +). +Braggio and Bonvicino (2004) +have recognized + +inermis + +and + +pachyurus + +as distinct species on the basis of karyotipic and sequence divergence. Even with the recognition of these two additional species, considerable geographic variation in karyotypes and sequence data remains among populations in +Brazil +. Specimens collected along the +Tocantins +and +Paraná +Rivers in the states of +Tocantins +and +Goiás +have a 2n=30 and a FN=56 ( + +Bonvicino et al., 2002 +b + +), whereas specimens from the states of +Bahia +and +Pernambuco +( + +T +. a. laurenteus + +) have a 2n=30 and FN=54 (Bonvicino et al., 2002; +Leal-Mesquita et al., 1993 +; +Souza and Yonenaga-Yassuda, 1982 +). Specimens collected from near the type locality ( + +T +. a. +apereoides + +) have a 2n=28 and a FN=50, whereas specimens from Jaborandi have a 2n=28 and a FN=52 (Bonvicino et al., 2002). More than a single species may still be present. +Braggio and Bonvicino (2004) +concluded based on analysis of sequence data that the karyotypic form with a 2n=30 and a FN=56 represents an undescribed species. Based on morphological differentiation +Reis et al. (2002) +suggested that more than one species was present within E +Brazil +, however, it is unclear how inclusion of material now recognized as + +inermis + +may have affected their analyses. + + + + \ No newline at end of file diff --git a/data/38/F7/BC/38F7BCCBF6137C617074789653D3ADE9.xml b/data/38/F7/BC/38F7BCCBF6137C617074789653D3ADE9.xml new file mode 100644 index 00000000000..acc449a40a4 --- /dev/null +++ b/data/38/F7/BC/38F7BCCBF6137C617074789653D3ADE9.xml @@ -0,0 +1,58 @@ + + + +The Formicidae (Hymenoptera) of Fennoscandia and Denmark. + + + +Author + +Collingwood, C. A. + +text + + +Fauna Entomologica Scandinavica + + +1979 + +8 + + +1 +174 + + + + +http://antbase.org/ants/publications/6175/6175.pdf + +journal article +6175 + + + + +Tetramorium simillimum +(Smith, 1851) + + + + +Myrmica simillima Smith +, 1851:118. + + + + +Workers and queen. Weakly sculptured, pale red much smaller than +T. guineense +. Length of worker: 1.6-2 mm, queen: 2.2-2.5 mm. Male. Light yellowish red; occiput rounded. Length: 2.5 mm. + + + +Biology. This cosmopolitan species occasionally occurs in heated glasshouses in Europe and has been recorded from Denmark and also on several occasions in England. + + + \ No newline at end of file diff --git a/data/38/F8/8C/38F88CC140B4CFD2405C475A77A978E5.xml b/data/38/F8/8C/38F88CC140B4CFD2405C475A77A978E5.xml new file mode 100644 index 00000000000..9ab46a66129 --- /dev/null +++ b/data/38/F8/8C/38F88CC140B4CFD2405C475A77A978E5.xml @@ -0,0 +1,115 @@ + + + +Type material of Platyhelminthes (Monogenoidea) housed in the Helminthological Collection of the Oswaldo Cruz Institute / FIOCRUZ (CHIOC), Rio de Janeiro, Brazil, from 1979 to 2016 + + + +Author + +Lopes, Daniela A. + + + +Author + +Mainenti, Adriana + + + +Author + +Sanches, Magda + + + +Author + +Knoff, Marcelo + + + +Author + +Gomes, Delir Correa + +text + + +ZooKeys + + +2016 + +616 + + +1 +75 + + + + +http://dx.doi.org/10.3897/zookeys.616.8481 + +journal article +http://dx.doi.org/10.3897/zookeys.616.8481 +1313-2970-616-1 +5A8C55011C4A458091CA41FFE5879A56 + + + + +Taxon +classification Animalia Gyrodactylidea Gyrodactylidae + + + + +Gyrodactylus samirae Popazoglo & Boeger, 2000 + + + +Type host. + +Corydoras ehrhardti +Steindachner, 1910 + + + +Infestation site. +Body surface. + + +Type locality. + +Brazil, +Parana +State, Piraquara, Piraquara River. + + + +Holotype. +CHIOC 34226 a. + + +Paratypes. + +CHIOC 34226 b, 34227, 34228, 34229 +a-g +. + + + +Remarks. +Other paratypes deposited in IPCR, MNHN, HWML and USNPC. + + +Reference. + +Popazoglo and Boeger (2000) +. + + + + \ No newline at end of file diff --git a/data/38/F8/DA/38F8DA10E27156A78D900E9D7D0C256D.xml b/data/38/F8/DA/38F8DA10E27156A78D900E9D7D0C256D.xml new file mode 100644 index 00000000000..1e909a2ea8e --- /dev/null +++ b/data/38/F8/DA/38F8DA10E27156A78D900E9D7D0C256D.xml @@ -0,0 +1,115 @@ + + + +Faunistic study of butterflies (Lepidoptera, Papilionoidea) of Sulaymaniyah Province, Kurdistan-Iraq + + + +Author + +Khudhur, Farhad A. +https://orcid.org/0000-0001-5267-6334 +University of Sulaimani, Sulaymaniyah, Kurdistan Region, Iraq & University of Mendel, Brno, Czech Republic +farhad.khudhur@univsul.edu.iq + +text + + +Biodiversity Data Journal + + +2022 + +2022-03-25 + + +10 + + +82612 +82612 + + + + +http://dx.doi.org/10.3897/BDJ.10.e82612 + +journal article +http://dx.doi.org/10.3897/BDJ.10.e82612 +1314-2828-10-e82612 +6D2A07B1C16450C8978279B6157E3DCC + + + + +Colotis fausta (Olivier, [1804]) + + + +Materials + + +Type status: + +Other material +. + +Location +: + +county: +Dukan +; locality: + +Qamchukha Village + +; verbatimCoordinates: +35°53'51"N +, +45°00'51"E + +Type status: +Other material +. +Location: +county: Sulyamaniyah; locality: Qlyasan; verbatimCoordinates: +35°34'41"N +, +45°22'01"E + + + + +Type status: +Other material +. +Location: +county: Bakrajo; locality: Kany Pan; verbatimCoordinates: +35°33'03"N +, +45°18'00"E + + +Type status: +Other material +. +Location: +county: Darbandikhan; locality: Sartak; verbatimCoordinates: +34°56'45"N +, +45°46'32"E + + +Type status: +Other material +. +Location: +county: Kalar; locality: Awa Khwery; verbatimCoordinates: +34°53'30"N +, +45°33'29"E + + + + + \ No newline at end of file diff --git a/data/38/F8/F1/38F8F104244C41E3733D7BEB701F6B5C.xml b/data/38/F8/F1/38F8F104244C41E3733D7BEB701F6B5C.xml new file mode 100644 index 00000000000..8f40e1958a7 --- /dev/null +++ b/data/38/F8/F1/38F8F104244C41E3733D7BEB701F6B5C.xml @@ -0,0 +1,157 @@ + + + +Flora Helvetica - Asteraceae + + + +Author + +Konrad Lauber + + + +Author + +Gerhart Wagner + + + +Author + +Andreas Gygax + +text + + +2018 +Haupt Verlag + +Bern + + + +Flora Helvetica + + + +1074 +1250 + + + +book chapter +978-3-258-08047-5 + + + + + +Arctium minus +Bernh. subsp. +minus + + + + + +Artbeschreibung: +Blaetter +unterseits locker graufilzig. Durchmesser der +Koepfe +1,5-2,5 cm +, + +innere +Huellblaetter +kuerzer +als die +Blueten + +. + + + + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +frisch; Feuchtigkeit +maessig +wechselnd ( ++/- +1-2 Stufen) +Lichtzahl LhalbschattigSalzzeichen--
Reaktionszahl Rneutral bis basisch (pH 5.5-8.5)Temperaturzahl T +montan ( +Waelder +mit Buche, Weisstanne, in den Zentralalpen mit +Waldfoehre +) +
+Naehrstoffzahl +N + +sehr +naehrstoffreich +bis +ueberduengt + +Kontinentalitaetszahl +K +subkontinental (niedrige relative Luftfeuchtigkeit, grosse Temperaturschwankungen, eher kalte Winter)
+
+
+ + +Volksname Deutscher Name: + +Gewoehnliche +Kleine Klette + +Nom +francais +: + +Bardane +a +petits capitules + + + +
+
\ No newline at end of file diff --git a/data/38/F9/67/38F9671FF643D6E65B5D63E090F4548E.xml b/data/38/F9/67/38F9671FF643D6E65B5D63E090F4548E.xml new file mode 100644 index 00000000000..437317ce957 --- /dev/null +++ b/data/38/F9/67/38F9671FF643D6E65B5D63E090F4548E.xml @@ -0,0 +1,62 @@ + + + +Pheidole in the New World. A dominant, hyperdiverse ant genus. + + + +Author + +Wilson, E. O. + +text + +2003 +Harvard University Press + +Cambridge, MA, USA + + + +http://atbi.biosci.ohio-state.edu/HymOnline/reference-full.html?id=20017 + +book +20017 + + + + +Pheidole fowleri +new species + +types Mus. Comp. Zool. Harvard. + + +Etymology Named after the prominent Brazilian myrmecologist H. G. Fowler. + + + +Diagnosis A member of the +diligens +group distinguished as follows. + + + +Major and minor: yellow; propodeal spines directed backward in side view, forming a 135-degree angle with the basal propodeal face; entire head, mesosoma, and waist foveolate and opaque. +Major: carinulae on head do not reach beyond level of eye, and are absent on the mesal half of the frontal lobes; hairs on entire profile of first gastral sternite short and subappressed; almost all of central strip of gastral tergites shagreened. +Minor: all of head, mesosoma, and waist foveolate and opaque; anterior half of central strip of first gastral tergite shagreened; in dorsal-oblique view, anterior face of propodeal dorsum drops precipitously to metanotum. +Measurements (mm) Holotype major: HW 1.00, HL 1.04, SL 0.66, EL 0.18, PW 0.52. +Paratype minor: HW 0.50, HL 0.54, SL 0.60, EL 0.14, PW 0.34. +color Major: concolorous reddish yellow. +Minor: concolorous plain dark yellow. + + +Range Known only from type locality in Mato Grosso; and from Goiania and Morrinhos Junction, Goias. Biology Collected in savanna (cerrado) at Morrinhos Junction and rocky forest near Goiania (W. L. Brown). + + + +figure Upper: holotype, major. Lower: paratype, minor. BRAZIL: Cuiaba, Mato Grosso (James C. Trager). Scale bars = 1 mm. + + + + \ No newline at end of file diff --git a/data/38/FA/B6/38FAB63A32E5C2D1522EE605DFF4F154.xml b/data/38/FA/B6/38FAB63A32E5C2D1522EE605DFF4F154.xml new file mode 100644 index 00000000000..6a24f8028e6 --- /dev/null +++ b/data/38/FA/B6/38FAB63A32E5C2D1522EE605DFF4F154.xml @@ -0,0 +1,75 @@ + + + +Checklist of aquatic and marshy Monocotyledons from the Araguaia River basin, Brazilian Cerrado + + + +Author + +Oliveira, Adriana + + + +Author + +Bove, Claudia + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +7085 +7085 + + + + +http://dx.doi.org/10.3897/BDJ.4.e7085 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e7085 +1314-2828--7085 + + + + +Rhynchospora barbata (Vahl) Kunth + + + +Materials + + +Type status: +Other material +. Occurrence: recordNumber: 218b; recordedBy: +C. P. Bove et al. +; Location: country: +Brazil +; countryCode: BRA; stateProvince: +Goias +; locality: + +Aruana-Araguapaz +road, Km 4 from +Aruana + +; verbatimLatitude: +14°56'6.55"S +; verbatimLongitude: +51°3'36.79"W +; verbatimCoordinateSystem: degree minutes; Event: year: 1997; month: 5; day: 29; Record Level: institutionID: Museu Nacional Herbarium; institutionCode: +R + + + + + \ No newline at end of file diff --git a/data/38/FA/BD/38FABDC34A7718CCA3D1F358E84CDD8D.xml b/data/38/FA/BD/38FABDC34A7718CCA3D1F358E84CDD8D.xml new file mode 100644 index 00000000000..9f361ba30d0 --- /dev/null +++ b/data/38/FA/BD/38FABDC34A7718CCA3D1F358E84CDD8D.xml @@ -0,0 +1,44 @@ + + + +Two new species of Metapone from Madagascar (Hymenoptera: Formicidae). + + + +Author + +Gregg, R. E. + +text + + +Proceedings of the Entomological Society of Washington + + +1958 + +60 + + +111 +121 + + + + +http://atbi.biosci.ohio-state.edu/HymOnline/reference-full.html?id=6291 + +journal article +6291 + + + + +Metapone tillyardi Wheeler + + + +Wheeler, Ann. Ent. Soc. Amer., 1919, 12, p. 187, [[worker]], Fig. 6. Type locality: Dorrigo, New South Wales + + + \ No newline at end of file diff --git a/data/38/FB/61/38FB611802869517F2B734F483F96176.xml b/data/38/FB/61/38FB611802869517F2B734F483F96176.xml new file mode 100644 index 00000000000..837c7cd1f8e --- /dev/null +++ b/data/38/FB/61/38FB611802869517F2B734F483F96176.xml @@ -0,0 +1,577 @@ + + + +Info Flora Schweiz - Apiaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/apiaceae.html + +url + + + + + +Carum carvi +L. + + + + + + +Kuemmel + + + + + +Art ISFS: 97100 Checklist: 1010610 +Apiaceae +Carum +Carum carvi L. + + +Zusammenfassung + + + + +Artbeschreibung + +(nach +Lauber & al. 2018 +) + +: +30-60 cm +hoch, kahl, sparrig verzweigt. + +Untere +Blaetter +2-3fach gefiedert + +, im Umriss +laenglich +, +Teilblaetter +letzter Ordnung fiederteilig, mit fein zugespitzten +Zaehnen +und Spitzen. + +Das unterste Teilblattpaar der untersten +Blaetter +auffallend nach unten +abgerueckt + +. Obere +Blaetter +viel kleiner und feiner. Dolden 8-16strahlig. + +Huelle +meist fehlend + +, +Huellchen +0-2 +blaettrig +. + +Blueten +weiss oder +roetlich + +. Frucht oval, 3-3,5 mm lang, kahl, zerrieben aromatisch. + + + + +Bluetezeit + +(nach +Lauber & al. 2018 +) + +: 5-8 + + +Standort und Verbreitung in der Schweiz + +(nach +Lauber & al. 2018 +) + +: Wiesen, Weiden / kollin-subalpin(-alpin) / CH + + + + +Verbreitung global + +(nach +Lauber & al. 2018 +) + +: Eurosibirisch + + + + +Oekologische +Zeigerwerte + +(nach +Landolt & al. 2010 +) + +333+42 + 3.k-t.2n=20,22 + + + +Status + + + +Status IUCN +: Nicht +gefaehrdet + + + + + +Oekologie + + +Lebensform Monokarper Hemikryptophyt, Therophyt + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + + + + + + + + +
+4.5.3 - Talfettweide (Kammgrasweide) ( +Cynosurion +) +
+4.5.4 - Bergfettweide (Milchkrautweide) ( +Poion alpinae +) +
+
+ + +fett + +Dominante Art, welche das Aussehen des Lebensraumes +mitpraegt + +Charakterart +Weniger strikt an den Lebensraum gebundene Art + + +
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +maessig +feucht +Lichtzahl LhellSalzzeichen1
Reaktionszahl Rschwach sauer bis neutral (pH 4.5-7.5)Temperaturzahl Tunter-subalpin und ober-montan
+Naehrstoffzahl +N + +maessig +naehrstoffarm +bis +maessig +naehrstoffreich + +Kontinentalitaetszahl +K + +subozeanisch bis subkontinental (mittlere Luftfeuchtigkeit, +maessige +Temperaturschwankungen und +maessig +tiefe Wintertemperaturen) +
+
+
+ + +Nomenklatur + + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Carum carvi +L. + + + + + + +Volksname Deutscher Name: + +Kuemmel + +Nom +francais +: + +Cumin des +pres + +Nome italiano: +Cumino tedesco +, + +Carvi + + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Carum carvi L. + + +Checklist 2017 + +97100
= +Carum carvi L. + + +Flora Helvetica 2001 + +1447
= +Carum carvi L. + + +Flora Helvetica 2012 + +1879
= +Carum carvi L. + + +Flora Helvetica 2018 + +1879
= +Carum carvi L. + + +Index synonymique 1996 + +97100
= +Carum carvi L. + + +Landolt 1977 + +2249
= +Carum carvi L. + + +Landolt 1991 + +1828
= +Carum carvi L. + + +SISF/ISFS 2 + +97100
= +Carum carvi L. + + +Welten & Sutter 1982 + +1172
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Status Indigenat +: Indigen + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein + + +Status Rote Liste national 2016 + + +Status IUCN +: Nicht +gefaehrdet + + + +Zusaetzliche +Informationen + +Kriterien IUCN: -- + + +Status Rote Liste regional 2019 + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Biogeografische RegionenStatusKriterien IUCN
Jura (JU) +nicht +gefaehrdet +(Least Concern) +
Mittelland (MP) +nicht +gefaehrdet +(Least Concern) +
Alpennordflanke (NA) +nicht +gefaehrdet +(Least Concern) +
+Alpensuedflanke +(SA) + +nicht +gefaehrdet +(Least Concern) +
+Oestliche +Zentralalpen (EA) + +nicht +gefaehrdet +(Least Concern) +
Westliche Zentralalpen (WA) +nicht +gefaehrdet +(Least Concern) +
+
+ + +Status nationale +Prioritaet +/Verantwortung + + + + + + + +
+Keine nationale +Prioritaet +oder internationale Verantwortung +
+
+ +Schutzstatus + + + + + + +
Kein internationaler, nationaler oder kantonaler Schutz
+
+
+
+
\ No newline at end of file diff --git a/data/38/FB/89/38FB895912113D1016091CA2368E7173.xml b/data/38/FB/89/38FB895912113D1016091CA2368E7173.xml new file mode 100644 index 00000000000..5ac6d7715a5 --- /dev/null +++ b/data/38/FB/89/38FB895912113D1016091CA2368E7173.xml @@ -0,0 +1,52 @@ + + + +An updated checklist of aquatic plants of Myanmar and Thailand + + + +Author + +Ito, Yu + + + +Author + +Barfod, Anders S. + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1019 +1019 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1019 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1019 +1314-2828--1019 + + + + +Cabomba caroliniana A. Gray., 1837 + + + +Distribution +Native to the Americas. + + + \ No newline at end of file diff --git a/data/38/FB/DE/38FBDEA4529FC94FBA740461258DB0FB.xml b/data/38/FB/DE/38FBDEA4529FC94FBA740461258DB0FB.xml new file mode 100644 index 00000000000..d36d040ae3e --- /dev/null +++ b/data/38/FB/DE/38FBDEA4529FC94FBA740461258DB0FB.xml @@ -0,0 +1,681 @@ + + + +Info Flora Schweiz - Betulaceae + + + +Author + +Info Flora + +text + +2021 +2023-10-20 +Info Flora Schweiz + +Geneve + + + +https://www.infoflora.ch/de/flora/betulaceae.html + +url + + + + + +Betula humilis +Schrank + + + + + +Niedrige Birke + + + + +Art ISFS: 60200 Checklist: 1006580 +Betulaceae +Betula +Betula humilis Schrank + + + +Bestimmungsschluessel + + + +Zusammenfassung + + + + +Artbeschreibung + +(nach +Lauber & al. 2018 +) + +: +Aehnlich +wie + +B. nana + +, aber 0,5- +3 m +hoch, +juengste +Triebe locker behaart bis kahl, + +mit vielen +Harzdruesen + +, +Blaetter +1-3 cm +lang, oval, + +nicht breiter als lang, mit spitzen +Zaehnen + +, am Grund oft +herzfoermig +. + + + + +Bluetezeit + +(nach +Lauber & al. 2018 +) + +: 5 + + +Standort und Verbreitung in der Schweiz + +(nach +Lauber & al. 2018 +) + +: Waldmoore / montan / SG + + + + +Verbreitung global + +(nach +Lauber & al. 2018 +) + +: Eurosibirisch + + + + +Oekologische +Zeigerwerte + +(nach +Landolt & al. 2010 +) + +5w31-433.n.2n=28 + + + +Status + + + +Status IUCN +: Vom Aussterben bedroht + + + + +Nationale +Prioritaet +: 1 - Sehr hohe nationale +Prioritaet + + +Internationale Verantwortung +: 2 - Mittel Erhalten/ +Foerdern +Gefaehrdungen +Isolierte Population, grosses Aussterberisiko +Rueckgang +des Samenkeimungspotenzials Mangel an geeigneten Mooren +fuer +Metapopulation Eutrophierung, Verschmutzung Intensive Nutzung des Umfeldes ( +Parkplaetze +, Sportanlagen etc.) Sukzession infolge fehlender Pflege, Verbuschung (Rubus), Beschattung + + + +Oekologie + + +Lebensform Nanophanerophyt + +Lebensraum Lebensraum +nach +Delarze & al. 2015 + + + + + +5.3.7 - +Moor-Weidengebuesch +( +Salicion cinereae +) + + + +
+
+
+ + +fett + +Dominante Art, welche das Aussehen des Lebensraumes +mitpraegt + +Charakterart +Weniger strikt an den Lebensraum gebundene Art + + +
+ + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F +ueberschwemmt +, bzw. unter Wasser; Feuchtigkeit +maessig +wechselnd ( ++/- +1-2 Stufen) +Lichtzahl LhellSalzzeichen--
Reaktionszahl Rschwach sauer bis neutral (pH 4.5-7.5)Temperaturzahl T +montan ( +Waelder +mit Buche, Weisstanne, in den Zentralalpen mit +Waldfoehre +) +
+Naehrstoffzahl +N + +sehr +naehrstoffarm + +Kontinentalitaetszahl +K + +subozeanisch bis subkontinental (mittlere Luftfeuchtigkeit, +maessige +Temperaturschwankungen und +maessig +tiefe Wintertemperaturen) +
+
+
+ + +Abhaengigkeit +vom Wasser + + + + + + + + + + + + + + + + + +
+Fluesse +1 - Zusatz- oder Nebenlebensraum
Ruhiges Wasser1 - Zusatz- oder Nebenlebensraum
Grundwasser0 - unbedeutend, keine Bindung.
+
+ +Nomenklatur + + + +Gueltiger +Name ( +Checklist 2017 +) + +: + +Betula humilis +Schrank + + +
+ + +Volksname Deutscher Name: +Niedrige Birke +, +Strand-Birke +Nom +francais +: + +Bouleau peu +eleve + +Nome italiano: +Betulla umile + + + + +Uebereinstimmung +mit anderen Referenzwerken + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
RelationNomReferenzwerkeNo
= +Betula humilis Schrank + + +Checklist 2017 + +60200
= +Betula humilis Schrank + + +Flora Helvetica 2001 + +255
= +Betula humilis Schrank + + +Flora Helvetica 2012 + +337
= +Betula humilis Schrank + + +Flora Helvetica 2018 + +337
= +Betula humilis Schrank + + +Index synonymique 1996 + +60200
= +Betula humilis Schrank + + +Landolt 1977 + +827
= +Betula humilis Schrank + + +Landolt 1991 + +728
= +Betula humilis Schrank + + +SISF/ISFS 2 + +60200
= +Betula humilis Schrank + + +Welten & Sutter 1982 + +131
+
+ + += Taxon stimmt mit akzeptiertem Taxon +ueberein +( +Checklist 2017 +) <Taxon ist im akzeptierten Taxon ( +Checklist 2017 +) enthalten> Taxon +enthaelt +(neben anderen) auch das akzeptierte Taxon ( +Checklist 2017 +) + + +
+ + +Status Indigenat +: Indigen + + + + +Liste der +gefaehrdeten +Pflanzen IUCN + +(nach +Walter & Gillett 1997 +): + +Nein + + +Status Rote Liste national 2016 + + +Status IUCN +: Vom Aussterben bedroht + + + +Zusaetzliche +Informationen + +Kriterien IUCN: C2a(i,ii); D + + +Status Rote Liste regional 2019 + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Biogeografische RegionenStatusKriterien IUCN
Jura (JU)--
Mittelland (MP)vom Aussterben bedroht (Critically Endangered)C2a(i,ii); D
Alpennordflanke (NA)regional beziehungsweise in der Schweiz ausgestorben (Regionally Extinct)
+Alpensuedflanke +(SA) +--
+Oestliche +Zentralalpen (EA) +--
Westliche Zentralalpen (WA)--
+
+ + +Status nationale +Prioritaet +/Verantwortung + + + + + + + + + + + + + + + + + + + + + + + + + +
+ +Nationale +Prioritaet + + +1 - Sehr hohe nationale +Prioritaet +
+Massnahmenbedarf +2 - Klarer Massnahmebedarf
+ +Internationale Verantwortung + +2 - Mittel
+ +Ueberwachung +Bestaende + + +2 - +Ueberwachung +ist +noetig +
+ +Schutzstatus + + + + + + + + + + + + + + +
+International (Berner Konvention) +Nein
+SG + +Teilweise +geschuetzt +( +Bluetezeit +) +(01.10.2017)
+
+ + + + + + + + +
+Schweiz +--
+
+
+ + +Erhalten/ +Foerdern +Gefaehrdungen +und Massnahmen Isolierte Population, grosses Aussterberisiko Unbedingt Pflege- und Regenerationskonzept erstellen Ex-situ-Vermehrung, Erhaltungskultur und Wiederansiedlungen wenn +moeglich +Rueckgang +des Samenkeimungspotenzials Ex-situ-Kultur weiterer +Herkuenfte +( +Baden-Wuerttemberg +) Mangel an geeigneten Mooren +fuer +Metapopulation Weitere Moortypen +fuer +(Wieder-) Ansiedlung schaffen (Konzept erforderlich) Eutrophierung, Verschmutzung Hydrologie +pruefen +Intensive Nutzung des Umfeldes ( +Parkplaetze +, Sportanlagen etc.) Erhaltung der naturnahen +Restflaechen +Sukzession infolge fehlender Pflege, Verbuschung (Rubus), Beschattung Starke Reduktion von Konkurrenzpflanzen Vorsichtiges Auslichten oder starke Auflichtung, wenn Folgepflege +gewaehrleistet +Mehr Informationen Merkblatt Artenschutz Amt +fuer +Natur, Jagd und Fischerei St.Gallen, 2019: Monitoring und Schutz +prioritaerer +Pflanzenvorkommen im Kanton St. Gallen 2016 - 2018 Schlussbericht A. Bona, U. Kulesza & K. A. Jadwiszczak, 2019: Clonal diversity, gene flow and seed production in endangered populations of +Betula humilis Schrk., Tree Genetics & Genomes +15: 50 + + +
+
\ No newline at end of file diff --git a/data/38/FC/25/38FC257AED58E8BF26BC013A92942EFD.xml b/data/38/FC/25/38FC257AED58E8BF26BC013A92942EFD.xml new file mode 100644 index 00000000000..faed01021de --- /dev/null +++ b/data/38/FC/25/38FC257AED58E8BF26BC013A92942EFD.xml @@ -0,0 +1,63 @@ + + + +Systema Naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis + + + +Author + +Linnaeus, Carolus + +text + +1758 +Laurentius Salvius + +Stockholm + + + +https://archive.org/download/mobot31753000798865/mobot31753000798865.pdf + +book +2C6327E1-5560-4DB4-B9CA-76A0FA03D975 +https://doi.org/10.5962/bhl.title.542 +3922206 + + + + +Phalaena trapezina +[ +spec. nov. +] + + + + +P. +Noctua +spirilinguis laevis, alis depressis pallidis fascia latissima saturatiore puncto nigro margineque punctato. + + +Mer. europ. t. +11. + + + + +Habitat in +Europa. + + + + +Alarum fascia trapeziformis est cum puncto nigro in +medio; +margo posticus supra punctorum nigrorum serie +notatus. + + + + \ No newline at end of file diff --git a/data/38/FC/2C/38FC2C360FB6FF14A814D938608092E2.xml b/data/38/FC/2C/38FC2C360FB6FF14A814D938608092E2.xml new file mode 100644 index 00000000000..ac8f3959103 --- /dev/null +++ b/data/38/FC/2C/38FC2C360FB6FF14A814D938608092E2.xml @@ -0,0 +1,62 @@ + + + +Brazilian Trichoptera Checklist II + + + +Author + +Paprocki, Henrique + + + +Author + +Franca, Diogo + +text + + +Biodiversity Data Journal + + +2014 + +2 + + +1557 +1557 + + + + +http://dx.doi.org/10.3897/BDJ.2.e1557 + +journal article +http://dx.doi.org/10.3897/BDJ.2.e1557 +1314-2828--1557 + + + + + +Leptonema tholloni +Navas +, 1923 + + + + +Distribution +Rio de Janeiro + + +Notes + +Flint et al. 1987 + + + + \ No newline at end of file diff --git a/data/38/FC/9C/38FC9CAC0CBA939A41B5BD6799565055.xml b/data/38/FC/9C/38FC9CAC0CBA939A41B5BD6799565055.xml new file mode 100644 index 00000000000..fd41d897bb3 --- /dev/null +++ b/data/38/FC/9C/38FC9CAC0CBA939A41B5BD6799565055.xml @@ -0,0 +1,82 @@ + + + +Hornmilben (Oribatida) [pages 261 to 322] + + + +Author + +Weigmann, G. + + + +Author + +Miko, L. + +text + + +2006 +Goecke & Evers + +Keltern + + + +Hornmilben (Oribatida) [Dahl, Tierwelt Deutschlands, Teil 76] + + + +261 +322 + + + + +http://www.goeckeevers.de/verlag/dahl.html + +book chapter +Weigmann2006pp261to322 + + + + +Cosmogneta kargi +Grandjean, 1963 [166d] + + + + +Diagnose: Lam verbreitert, vorn lang parallel und eng beieinander; le +blattfoermig +verdickt; mit Bothridial- und +Interlamellarhoeckern +; ss distal einseitig mit +kraeftigen +Papillen bzw. Dornen besetzt (Gattungsmerkmale); ng kurz, glatt und +duenn +; 6 g, +Koerperlaenge +300-320 µm. + + + +Syn., Tax.: Grandjean 1963d. + + + +Oekologie +: Unklar. + + + + +Verbreitung: Deutschland, +Suedfrankreich +. + + + + \ No newline at end of file diff --git a/data/38/FC/B3/38FCB30A95695A5A838AF60C19D7C421.xml b/data/38/FC/B3/38FCB30A95695A5A838AF60C19D7C421.xml new file mode 100644 index 00000000000..bccf6b5902e --- /dev/null +++ b/data/38/FC/B3/38FCB30A95695A5A838AF60C19D7C421.xml @@ -0,0 +1,154 @@ + + + +A revision of Pachyballus Simon, 1900 and Peplometus Simon, 1900 (Araneae, Salticidae, Ballini) with descriptions of new species + + + +Author + +Wesolowska, Wanda +Department of Biodiversity and Evolutionary Taxonomy, University of Wroclaw, Przybyszewskiego 65, 51 - 148 Wroclaw, Poland + + + +Author + +Azarkina, Galina N. +Laboratory of Systematics of Invertebrate Animals, Institute of Systematics and Ecology of Animals, Siberian Branch Russian Academy of Sciences, Frunze Street 11, Novosibirsk 630091, Russia +https://orcid.org/0000-0002-9328-3913 + + + +Author + +Wisniewski, Konrad +Institute of Biology and Earth Sciences, Pomeranian University in Slupsk, Arciszewskiego 22 b, 76 - 200 Slupsk, Poland + +text + + +ZooKeys + + +2020 + +944 + + +47 +98 + + + + +http://dx.doi.org/10.3897/zookeys.944.49921 + +journal article +http://dx.doi.org/10.3897/zookeys.944.49921 +1313-2970-944-47 +CBF1BE5BD1E5408B8769E8FA935D6C78 +530549BF5AD95FF7B321BF51843EAD48 + + + + +Pachyballus variegatus Lessert, 1925 +Figures 123-128 +, 193 + + + + +Pachyballus variegatus +Lessert 1925: 437, f. 10-14 (♂♀). + + + +Syntypes. + +Tanzania • 1♂ 1♀; Kilimanjaro, Kibonoto; +3°11'S +, +37°06'E +; +Sjoestedt +leg.; NHRS; examined. + + + +Diagnosis. + +This species is the only one in the genus that does not have the posterior ventral scutum on abdomen. Its other diagnostic feature is the pattern on abdomen; the anterior one-fourth of the abdomen is bright, the posterior part dark with a wide, light median patch (Figs +123 +, +127 +). + + + +Redescription. + +Male. +Measurements: Cephalothorax: length 1.4, width 1.3, height 0.4. Eye field: length 0.7, anterior width 1.1, posterior width 1.3. Abdomen: length 1.8, width 1.7. + + +General appearance as in Fig. +123 +. Body flattened, integument strongly sclerotised, clearly pitted. Eye field light, yellowish orange, blackish rings around eyes, thoracic part light brown anteriorly, posterior slope yellowish. A few delicate hairs at anterior eyes. Chelicerae brown, with three teeth on promargin and a tooth with two tips on retromargin (Fig. +124 +). Labium and endites basally brownish, with light tips. Sternum light brown. Abdomen heart-shaped, widest anteriorly and tapering, anteriorly orange, sides brown with wide orange area in the middle (Fig. +123 +). Venter yellowish, without scutum. Spinnerets short, yellow. Legs relatively short, dark yellow (first pair absent in the syntype, only coxae extant, brown). Pedipalp (only right present) brown. Palpal organ as in Figs +125 +, +126 +, embolic coil wide, with three loops. + + + +Figures 123-128. + +Pachyballus variegatus + +, syntypes +123 +male, habitus +124 +cheliceral dentition +125 +palpal organ, ventral view +126 +palpal organ, lateral view +127 +female, colouration of abdomen +128 +epigyne. + + + +Female. +Measurements: Cephalothorax: length 1.5, width 1.4, height 0.5. Eye field: length 0.8, anterior width 1.2, posterior width 1.4. Abdomen: length 2.2, width 2.1. + + +Colouration as in male (Fig. +127 +). Abdomen rounded. Palp light, with brown apical part. Epigyne weakly sclerotised with shallow central depression (Fig. +128 +). Internal structure not studied, spermathecae probably large (visible through integument). + + + +Remarks. +Lessert (1925) wrote in the original description that the basic colour of body was black. The specimens must have bleached heavily, however the outline of lighter patches has been preserved. + + +Distribution. + +Known only from the type locality (Fig. +193 +). + + + + \ No newline at end of file diff --git a/data/38/FC/C2/38FCC23388B147D63A8D67FF5E73C571.xml b/data/38/FC/C2/38FCC23388B147D63A8D67FF5E73C571.xml new file mode 100644 index 00000000000..9da8d941b85 --- /dev/null +++ b/data/38/FC/C2/38FCC23388B147D63A8D67FF5E73C571.xml @@ -0,0 +1,56 @@ + + + +Checklist of British and Irish Hymenoptera - Ichneumonidae + + + +Author + +Broad, Gavin R. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +9042 +9042 + + + + +http://dx.doi.org/10.3897/BDJ.4.e9042 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e9042 +1314-2828-4-9042 + + + + +Rhinotorus mesocastanus (Thomson, 1892) + + + + +Spudaeus mesocastanus +Thomson, 1892 + + + +Distribution +England + + +Notes +BMNH, det. Reshchikov, added here + + + \ No newline at end of file diff --git a/data/38/FC/D6/38FCD6C35BD6F26016C9C108CA324CEF.xml b/data/38/FC/D6/38FCD6C35BD6F26016C9C108CA324CEF.xml new file mode 100644 index 00000000000..8ac06719ba3 --- /dev/null +++ b/data/38/FC/D6/38FCD6C35BD6F26016C9C108CA324CEF.xml @@ -0,0 +1,148 @@ + + + +Flora Helvetica - Orchidaceae + + + +Author + +Konrad Lauber + + + +Author + +Gerhart Wagner + + + +Author + +Andreas Gygax + +text + + +2018 +Haupt Verlag + +Bern + + + +Flora Helvetica + + + +1324 +1362 + + + +book chapter +978-3-258-08047-5 + + + + + +Dactylorhiza incarnata +(L.) +Soo +subsp. +incarnata + + + + + +Artbeschreibung: +Blaetter +straff aufrecht oder leicht +zurueckgebogen +. + +Blueten +rosa bis purpurn + +, Lippe ungeteilt oder undeutlich 3teilig, mit deutlichem Schleifenmuster. + + + + +Bluetezeit +: 5-6 + +Standort und Verbreitung in der Schweiz: Feuchte Wiesen, Flachmoore / kollin-montan(-subalpin) / CH + + +Verbreitung global: Eurasiatisch + + + +Oekologische +Zeigerwerte nach +Landolt & al. (2010) + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+Bodenfaktoren + +Klimafaktoren + +Salztoleranz +
Feuchtezahl F--Lichtzahl L--Salzzeichen--
Reaktionszahl R--Temperaturzahl T--
+Naehrstoffzahl +N +-- +Kontinentalitaetszahl +K +--
+
+
+ + +Volksname Deutscher Name: +Fleischrote Fingerwurz +, +Fleischfarbige Fingerwurz +Nom +francais +: + +Orchis +incarnat + +Nome italiano: +Orchide palmata + + +
+
\ No newline at end of file diff --git a/data/38/FD/92/38FD927FAFE9EB4DF8AF200B35E9DCDE.xml b/data/38/FD/92/38FD927FAFE9EB4DF8AF200B35E9DCDE.xml new file mode 100644 index 00000000000..f762a012aa8 --- /dev/null +++ b/data/38/FD/92/38FD927FAFE9EB4DF8AF200B35E9DCDE.xml @@ -0,0 +1,97 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part S) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +806 +877 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Seriola urens +(Linnaeus) Linnaeus + +, + +Species Plantarum +, ed. 2, 2 + +: 1139. 1763 + + +. + + + +"Habitat in Sicilia." RCN: 5909. + + + +Basionym: + +Hypochaeris urens +L. (1753) + +. + + + + +Neotype +(Turland in Jarvis & Turland in +Taxon +47: 363. 1998): Italy. Sicilia: Palermo, S. Martino, in pascuis apricis submontosis, +Todaro 1257 +[Todaro, +Flora Sicula Exsiccata +] (BM-000576306). + + + + +Current name: + + +Hypochaeris cretensis + +(L.) Bory & Chaub. + +( +Asteraceae +). + + + + \ No newline at end of file diff --git a/data/38/FD/9B/38FD9B40382252F58D03F78FCE1D83C8.xml b/data/38/FD/9B/38FD9B40382252F58D03F78FCE1D83C8.xml new file mode 100644 index 00000000000..cb95a298673 --- /dev/null +++ b/data/38/FD/9B/38FD9B40382252F58D03F78FCE1D83C8.xml @@ -0,0 +1,118 @@ + + + +Annotated catalog and bibliography of the cyclocephaline scarab beetles (Coleoptera, Scarabaeidae, Dynastinae, Cyclocephalini) + + + +Author + +Moore, Matthew R. +Department of Entomology and Nematology, University of Florida, Building 1881 Natural Area Drive, Steinmetz Hall, Gainesville, FL 32611, USA +cyclocephala@gmail.com + + + +Author + +Cave, Ronald D. +Department of Entomology and Nematology, University of Florida, Indian River Research and Education Center, 2199 South Rock Road, Fort Pierce, FL 34945, USA + + + +Author + +Branham, Marc A. +Department of Entomology and Nematology, University of Florida, Building 1881 Natural Area Drive, Steinmetz Hall, Gainesville, FL 32611, USA + +text + + +ZooKeys + + +2018 + +2018-03-22 + + +745 + + +101 +378 + + + + +http://dx.doi.org/10.3897/zookeys.745.23685 + +journal article +http://dx.doi.org/10.3897/zookeys.745.23685 +1313-2970-745-101 +8785DC6BC2A244FD94B6243EB07C717F +047DFFCAFFA5F32EA97C873F4708943F +1222435 + + + + + +Cyclocephala crassa +Endrodi +, 1967 + + + + + +Cyclocephala crassa +Endrodi +, 1967c: 1-3 [original combination]. + + + +Types. + +Holotype ♂ at ZMHB ( + +Endrodi +1967c + +). + + + +Distribution. +COLOMBIA: Amazonas. ECUADOR. + + +References. + + +Martinez +1975b + +, +Pike et al. 1976 +, + +Endrodi +1967c + +, +1985a +, Restrepo et al. 2003, +Krajcik 2005 +, +2012 +, + +Gasca-Alvarez +and Deloya 2016 + +. + + + + \ No newline at end of file diff --git a/data/38/FD/EA/38FDEAA122EF5CF4A8DAD52AFE41078B.xml b/data/38/FD/EA/38FDEAA122EF5CF4A8DAD52AFE41078B.xml new file mode 100644 index 00000000000..fc18baf5d0d --- /dev/null +++ b/data/38/FD/EA/38FDEAA122EF5CF4A8DAD52AFE41078B.xml @@ -0,0 +1,169 @@ + + + +Census of the longhorn beetles (Coleoptera, Cerambycidae and Vesperidae) of the Macau SAR, China + + + +Author + +Lin, Mei-Ying +Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, 1 - 5 Beichen West Road, Chaoyang Dist., Beijing, 100101, China + + + +Author + +Perissinotto, Renzo +Institute for Coastal & Marine Research (CMR), Nelson Mandela University, P. O. Box 77000, Gqeberha 6031, South Africa +renzo.perissinotto@mandela.ac.za + + + +Author + +Clennell, Lynette +Macau Anglican College, 109 - 117 Avenida Padre Tomas Pereira, Taipa, Macau SAR, China + +text + + +ZooKeys + + +2021 + +2021-07-22 + + +1049 + + +79 +161 + + + + +http://dx.doi.org/10.3897/zookeys.1049.65558 + +journal article +http://dx.doi.org/10.3897/zookeys.1049.65558 +1313-2970-1049-79 +5D5EC2F0E9854C6EB55B5AD879C78A16 +2DD0CB1DF6045A1DA8B1DDF6163DC76F + + + + +Ceresium sinicum ornaticolle Pic, 1907 + + + + +Fig. 12 + + + + +Ceresium ornaticolle +Pic, 1907: 20. TL: China (Yunnan); TD: MNHN. + + + +Distribution. + +Palaearctic Region: China (Fujian, Guangdong, Guangxi, Guizhou, Hong Kong, Hubei, Hunan, Jiangsu, Jiangxi, Shaanxi, Shanxi, Sichuan, Xizang, Yunnan, Zhejiang) ( +Yiu 2009 +; +Lin and Yang 2019 +; +Danilevsky 2020 +). Oriental Region: Laos; Vietnam ( +Gressitt and Rondon 1970 +). + + + +Figure 12. + +Ceresium sinicum ornaticolle + +Pic, 1907: dorsal ( +A +) and lateral ( +B +) views of specimens observed on Great Taipa (3 Mar 2019) and at the +Hac-Sa +Dam in Coloane (12 Apr 2020), respectively (photographs: +A +LC +B +Kit Chang). + + + + +Macau records. + +Great Taipa, 3 Mar 2019, at light in ablution block, R Perissinotto & L Clennell; ibidem16 Mar 2019, R Perissinotto; ibidem 13 Jun 2019, R Perissinotto & L Clennell (IZCAS); Coloane Heights, 28 Apr 2019, at light in ablution block, R Perissinotto & L Clennell (IZCAS); Coloane +Hac-Sa +, 8 Apr 2020, on flowers of + +Ligustrum sinense + +, R Perissinotto & L Clennell); Coloane +Ka-Ho +, 22 May 2020, dead on tree trunk, R Perissinotto & L Clennell (IZCAS, MACT); +Mong-Ha +Hill Municipal Park, 30 Apr 2019 22:47, Eric Kwan (https://www.inaturalist.org/observations/24195774); [Coloane] +Hac-Sa +Dam, 21 Apr 2019 15:29, Kit Chang (https://www.inaturalist.org/observations/23059827); [Coloane] St. Francis +Xavier's +Parish, 12 Apr 2020 21:33, Kit Chang (https://www.inaturalist.org/observations/48646082); ibidem 13 Apr 2020 21:50, Kisu Wong (https://www.inaturalist.org/observations/49577131); Taipa Grande, 12 May 2021, Lynette Clennell (https://www.inaturalist.org/observations/78523364). + + + +Remarks. + +In Macau, this species ranges 11-13 mm in total length and 2.5-3 mm in maximum width. During the current census it has been observed mainly at night under artificial lights, however on one occasion it was found during daytime feeding on flowers of + +Ligustrum sinense + +. In nearby Hong Kong, larvae have been documented to bore into wood of + +Cinnamomum camphora + +, + +Citrus + +spp., and + +Melia azedarach + +( +Yiu 2009 +). +Liu (1992) +reported them as serious pests of + +Punica granatum + +in Sichuan, but also more generally of + +Malus domestica + +, + +Pyrus + +sp. and + +Ricinus communis + +. + + + + \ No newline at end of file diff --git a/data/38/FD/EC/38FDECE42FD03C25BF6496AE40411434.xml b/data/38/FD/EC/38FDECE42FD03C25BF6496AE40411434.xml new file mode 100644 index 00000000000..e08c9d58ed8 --- /dev/null +++ b/data/38/FD/EC/38FDECE42FD03C25BF6496AE40411434.xml @@ -0,0 +1,92 @@ + + + +Chapter 7: Linnaean Plant Names and their Types (part A) + + + +Author + +Jarvis, Charlie +Department of Botany, Natural History Museum, Cromwell Road, London, UK + +text + + +2007 +Linnaean Society of London in association with the Natural History Museum + +London + + + +Order out of Chaos. Linnaean Plant Types and their Types + + + +252 +342 + + + +book chapter +https://doi.org/10.5281/zenodo.291971 +978-0-9506207-7-0 +291971 + + + + + + + +Achyranthes muricata +Linnaeus + +, + +Species Plantarum +, ed. 2, 1 + +: 295. 1762 + + +. + + + + +"Habitat in +India +." RCN: 1656. + + + + + +Lectotype +(Townsend in Nasir & Ali, +Fl. W. Pakistan +71: 23. 1974): Herb. Linn. No. 287.6 ( +LINN +) + +. + + + + +Current name: + + +Digera muricata + +(L.) Mart. + +( +Amaranthaceae +). + + + + \ No newline at end of file diff --git a/data/38/FD/F2/38FDF2502C92D964FFBA34C4413D1BE1.xml b/data/38/FD/F2/38FDF2502C92D964FFBA34C4413D1BE1.xml new file mode 100644 index 00000000000..a9da3db3455 --- /dev/null +++ b/data/38/FD/F2/38FDF2502C92D964FFBA34C4413D1BE1.xml @@ -0,0 +1,52 @@ + + + +Catalogue of hymenopterous insects collected by Mr. A. R. Wallace in the Islands of Ceram, Celebes, Ternate, and Gilolo. + + + +Author + +Smith, F. + +text + + +Journal of the Proceedings of the Linnean Society of London, Zoology + + +1861 + +6 + + +36 +48 + + + + +http://antbase.org/ants/publications/2596/2596.pdf + +journal article +2596 +478E0DB4-21A2-4A50-B59D-774B53696A70 + + + + +1. +Polyrhachis hastatus + + + +, Latr. Hist. Nat. Fourm. p. 129, pl. 4. fig. 23, [[ queen ]]. + + +Hab. Celebes; India. + + +The specimen from Celebes has the metathoracic spines shorter than Indian specimens which I have seen, and those on the node of the peduncle are also rather shorter; however, in its opake blackness and in every other particular the insect is identical. + + + \ No newline at end of file diff --git a/data/38/FE/10/38FE10CF269F560B80BC82D77309B4A3.xml b/data/38/FE/10/38FE10CF269F560B80BC82D77309B4A3.xml new file mode 100644 index 00000000000..c025fc3bbac --- /dev/null +++ b/data/38/FE/10/38FE10CF269F560B80BC82D77309B4A3.xml @@ -0,0 +1,75 @@ + + + +A checklist of vascular plants of the W National Park in Burkina Faso, including the adjacent hunting zones of Tapoa-Djerma and Kondio + + + +Author + +Nacoulma, Blandine M. I. +Universite Joseph Ki-Zerbo, Ouagadougou, Burkina Faso + + + +Author + +Schmidt, Marco +Senckenberg Biodiversity and Climate Research Centre, Frankfurt am Main, Germany & Palmengarten, Frankfurt am Main, Germany +https://orcid.org/0000-0001-6087-6117 +mschmidt@senckenberg.de + + + +Author + +Hahn, Karen +Goethe University, Frankfurt am Main, Germany + + + +Author + +Thiombiano, Adjima +Universite Joseph Ki-Zerbo, Ouagadougou, Burkina Faso + +text + + +Biodiversity Data Journal + + +2020 + +8 + + +54205 +54205 + + + + +http://dx.doi.org/10.3897/BDJ.8.e54205 + +journal article +http://dx.doi.org/10.3897/BDJ.8.e54205 +1314-2828-8-e54205 +AC04300B71A5532C90F2702393102067 + + + + +Ludwigia octovalvis (Jacq.) P.H.Raven + + + +Distribution +Pluriregional African + + +Notes +Life Form: therophyte; Voucher: Schumann (FR-0083245) + + + \ No newline at end of file diff --git a/data/38/FF/04/38FF0477886D7E140552AC24AFA94D8D.xml b/data/38/FF/04/38FF0477886D7E140552AC24AFA94D8D.xml new file mode 100644 index 00000000000..bc1973ce06e --- /dev/null +++ b/data/38/FF/04/38FF0477886D7E140552AC24AFA94D8D.xml @@ -0,0 +1,149 @@ + + + +Chenopodiaceae - Fumariaceae (Chenopodium) + + + +Author + +Jonsell, B., Karlsson + +text + + +Flora Nordica + + +2005 + +2 + + +4 +31 + + + + +http://antbase.org/ants/publications/FlNordica_chenop/FlNordica_chenop.pdf + +journal article +FlNordica_chenop + + + + +7. +Chenopodium urbicum L. +Figs 2G, 6B + + + + +Linnaeus, Sp. pi.: 218 (1753). + + + + +- Type: Linnaean Herbarium 313.2 (LINN) lectotype, sei. by +Uotila, Ann. Bot. Fenn. 30: 190 (1993) +. + + + + +D Rank +Gasefod +. F +kylaesavikka +. N bymelde. S +bymalla +. + + + + +Literature. +Nilsson & Gustafsson 1979 +. + + + + +Therophyte (summer-annual). 10-60(-100) cm, glabrous or sometimes farinose, olive-green or sometimes brownish. Stem angular, yellowish, never red in the leaf axils, hard, erect, sparsely branched. Lower and middle leaves with petiole less than half as long as the blade; blade fairly thick, ++/- +broadly triangular, sometimes as wide as long, often with outward-pointing basal lobes, 3-10(-18) x 3-8(-20) cm; base ++/- +truncate (slightly cuneate to slightly cordate); apex obtuse or sometimes acute; margin sinuate to dentate with teeth pointing outwards or sometimes recurved, or rarely subentire; teeth at the widest point of the blade larger than the others. Upper leaves with narrowly triangular to trullate or lanceolate blade. + +Inflorescences axillary and terminal, erect, spikelike, ebracteate; glomerules very small, dense. Flowers monomorphic, bisexual or female. Tepals 5, connate at base, not keeled, with wide membranous margin; apex obtuse. Stamens 5. Stigmas 2 or sometimes 3, 0.1 mm. Nut falling with or without the perianth; pericarp not or weakly adherent to the seed. Seed horizontal, orbicular in outline, 1-1.2 mm; edge rounded; seed-coat black, glossy, almost smooth to obscurely reticulate or rugulose. - Mid-summer to early autumn. +[2n=36] + + + +Distribution. Archaeophytic at least in parts of F and S (but now extinct); also a casual alien, in D and N perhaps never established. - D +OJy +Vejle 1930, 1932, + +Arhus + +1999, FyL Svendborg 1905; Sjce +Kobenhavn +1985, Farum 1990-97 (with compost from the botanic garden in +Kobenhavn +); a few records from +Sjae +, LFM and Brn in the period 1825-1939. N 0/Halden 1827, Ak Oslo and +Baerum +(both before 1900), Ho Etne 1959 (poultry farm). S formerly scattered to rare north to Vrm, Vsm and Gst and fairly abundant in some towns (e.g. Gtl Visby, Upl Uppsala), nowadays disappeared, last seen as established in Vsm Bro 1987; casual north to Mpd and in Nb\ most recently recorded, as a casual, in Bl Ramdala 1989, Kim +Torsas +1999, Smi +Tingsas +1999, 2000, BhG +Goeteborg +1993 and Nb Nederkalix 1997. F in the 19th century apparently ++/- +established as an archaeophyte or a relatively old alien in some old towns and villages (at leasts +Finstroem +, Saltvik, Sund, Kumlinge, V Korppoo, +Saerkisalo +, U Inkoo, Helsinki, Porvoo, +Myrskylae +, EK Kotka and EH +Sysmae +), now disappeared; casual occurrences, most often of Russian origin, after 1950 at least in U Helsinki 1950's to 1960's, EH Nokia 1972 (tip), Tampere 1961, 1963 (railway yard), 1976 (mill), ES Savonlinna 1950's (tip), EP Vaasa 1950's (docks), PK +Vaertsilae +1990 (railway yard) and OP Oulu 1960 (docks). + +Europe (especially the SE part); from SW Asia to Siberia; also North America (not native). + + +Habitat. Very nitrophilous, but a poor competitor. Nitrogen-rich places in farmland (dungheaps, cowhouses and farmyards), in the 18th and 19th centuries also town streets; in the later part of the 20th century mainly as a casual (railway yards, ports, fields and grain mills). The disappearance is probably mainly due to improved sanitary conditions. + + + +Variation. Variants based on differences in leaf shape have sometimes been recognized. Nordic plants have broadly triangular leaf-blades and seem to match +var. urbicum +fairly well. + + +Similar taxa. +Chenopodium urbicum +is similar to +C. macrospermum +(rare casual). - Sometimes mixed up with +C. chenopodioides +(4), +C. murale +(9), +Atriplex prostrata +and +A. hortensis +. The species of +Atriplex +can be distinguished even in the vegetative phase by (sub)opposite branches and leaves. + + + + \ No newline at end of file diff --git a/data/38/FF/0E/38FF0EAF99495E2282FB74F3B93443BE.xml b/data/38/FF/0E/38FF0EAF99495E2282FB74F3B93443BE.xml new file mode 100644 index 00000000000..2f95997cc56 --- /dev/null +++ b/data/38/FF/0E/38FF0EAF99495E2282FB74F3B93443BE.xml @@ -0,0 +1,85 @@ + + + +New records and checklist of Chilocorini (Coleoptera: Coccinellidae) from China + + + +Author + +Li, Wenjing +Guangdong Provincial Key Laboratory of High Technology for Plant Protection, Plant Protection Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou, China +https://orcid.org/0000-0002-3365-1219 + + + +Author + +Chen, Bingxu +Guangdong Provincial Key Laboratory of High Technology for Plant Protection, Plant Protection Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou, China + + + +Author + +Huo, Lizhi +Key Laboratory of Bio-Pesticide Innovation and Application, Engineering Technology Research Center of Agricultural Pest Biocontrol, Guangdong Province; Engineering Research Center of Biological Control, Ministry of Education & Guangdong Province, South China Agricultural University, Guangzhou, China + + + +Author + +Chen, Xiaosheng +Key Laboratory of Bio-Pesticide Innovation and Application, Engineering Technology Research Center of Agricultural Pest Biocontrol, Guangdong Province; Engineering Research Center of Biological Control, Ministry of Education & Guangdong Province, South China Agricultural University, Guangzhou, China +https://orcid.org/0000-0001-8253-4943 + + + +Author + +Wang, Xingmin +Key Laboratory of Bio-Pesticide Innovation and Application, Engineering Technology Research Center of Agricultural Pest Biocontrol, Guangdong Province; Engineering Research Center of Biological Control, Ministry of Education & Guangdong Province, South China Agricultural University, Guangzhou, China +32457430@qq.com + +text + + +Biodiversity Data Journal + + +2020 + +8 + + +51092 +51092 + + + + +http://dx.doi.org/10.3897/BDJ.8.e51092 + +journal article +http://dx.doi.org/10.3897/BDJ.8.e51092 +1314-2828-8-e51092 +AD6F8FCD4AE850068DBA551EEB676FB7 + + + + +Chilocorus yunlongensis Cao & Xiao, 1984 + + + +Distribution + +China ( +Cao and Xiao 1984 +, +Li et al. 2018 +). + + + + \ No newline at end of file diff --git a/data/38/FF/16/38FF168EE573E193E5A4F022FCE72A20.xml b/data/38/FF/16/38FF168EE573E193E5A4F022FCE72A20.xml new file mode 100644 index 00000000000..8c28f5b15c9 --- /dev/null +++ b/data/38/FF/16/38FF168EE573E193E5A4F022FCE72A20.xml @@ -0,0 +1,179 @@ + + + +Flora der Schweiz und angrenzender Gebiete. Band 2. Nymphaceae bis Primulaceae (2 nd edition) (p. 956): Rosaceae + + + +Author + +Hess, Hans Ernst + + + +Author + +Landolt, Elias + + + +Author + +Hirzel, Rosmarie + +text + +1976 +Birkhaeuser Verlag + + +https://doi.org/10.5281/zenodo.292251 + +book +292251 +10.5281/zenodo.292251 +3-7643-0527-4 + + + +<subSubSection id="DF5B83436B7BFF9F1D415624391956AE" pageId="null" pageNumber="384" type="nomenclature"> +<paragraph id="6E80B57A93502B384A0923DEC5B297F0" pageId="null" pageNumber="384"> +<taxonomicName id="AC8E31288B9AE35D1B570E01F308A5FD" authority="L." class="Magnoliopsida" family="Rosaceae" genus="Potentilla" kingdom="Plantae" order="Rosales" pageId="null" pageNumber="384" phylum="Tracheophyta" rank="species" species="fruticosa"> +<pageBreakToken id="01106658FEC1A8BACDA9373BC60B7FE5" pageId="null" pageNumber="384" start="start">Potentilla</pageBreakToken> +<normalizedToken id="82C4B711C672C49078EE6CC07B4797A1" originalValue="fruticósa" pageId="null" pageNumber="384">fruticosa</normalizedToken> +<authorityName id="62828DDB9D340BB00663E311424BED2D" pageId="null" pageNumber="384">L.</authorityName> +</taxonomicName> +</paragraph> +</subSubSection> +<subSubSection id="3A831FAA6309A7531B4C8A838AD6407F" pageId="null" pageNumber="384" type="vernacular_names"> +<paragraph id="DCB66F8908DA65F053C7560F39228DBC" pageId="null" pageNumber="384">Strauch-Fingerkraut</paragraph> +</subSubSection> + + + +0,2-1,5 m hoher, verholzter, im Alter sparrig verzweigter Strauch +(alle folgenden Arten nicht +strauchfoermig +). +Juengste +Triebe behaart, +aeltere +kahl; Rinde braun, sich in Fetzen +abloesend +. +Blaetter +meist weniger als 1 cm lang gestielt, +1fach gefiedert +, 3-5 oder 7 +zaehlig +; +Teilblaetter +oval, 1-2 cm lang, 3-4mal so lang wie breit, die 3 obersten am Stiel herablaufend, die untern sitzend, oberseits +dunkelgruen +, unterseits heller, beiderseits behaart bis fast kahl, mit nach unten umgebogenem Rand. +Blueten +einzeln oder zu wenigen an +beblaetterten +Trieben, Durchmesser 1,8-2,5 cm. +Bluetenstiele +schief abstehend behaart. +Aussenkelchblaetter +schmal lanzettlich, deutlich +laenger +als die innern +Kelchblaetter +. + +Kronblaetter +gelb + +, vorn rundlich, nach dem Grunde +keilfoermig +verschmaelert +, die +Kelchblaetter +weit +ueberragend +. + +Fruechtchen +dicht und lang behaart, mit +grundstaendigem +, nach oben deutlich verdicktem Griffel; + +Narbe 1-1,5 mm lang, nach oben deutlich verdickt. - +Bluete +: +Fruehsommer +bis Herbst. + + +Zytologische Angaben. 2n += +14: +Material aus +Suedeuropa +, Zentral-, Ost- und Nordostasien, Nordamerika ( +Blueten +zwitterig). +2n += +28: +Material aus Nordeuropa (Irland, England, Schweden) ( +Blueten +eingeschlechtig). +2n += +42: +Material aus Zentralasien (Altai). Zusammenstellung der vielen +Chromosomenzaehlungen +aus Wildpopulationen, Verbreitungskarten, +grosses +Literaturverzeichnis von Elkington (1969). + + +Standort. +Im Norden in den Niederungen in feuchten +Ufergebueschen +; im +Sueden +in den Gebirgen in steinigen Halden bis 3000 m, im Himalaja bis 5000 m; im Gebiet Gartenpflanze, selten verwildert. + + +Verbreitung. Eurasiatisch-nordamerikanische Pflanze: +Irland, England, +Suedschweden +, Baltikum, Ural; +Pyrenaeen +, Seealpen; im +uebrigen +Europa +haeufig +kultiviert; Kaukasus, Nordasien (bis +Eismeerkueste +), Zentral- und Ostasien ( +Suedgrenze +durch den Himalaja); in Nordamerika von 70° NB +suedwaerts +bis Neumexiko und New Jersey. Verbreitungskarte von Meusel et al. (1965). - Im Gebiet +haeufig +kultiviert, im +Elsass +verwildert. + + +Bemerkungen. +Entwicklungszentrum der +strauchfoermigen +Potentilla- +Arten in Zentral- und Ostasien (Elkington 1969). Viele biologische Angaben +ueber + +P. fruticosa +von Elkington (1963a) + +. + + + + \ No newline at end of file diff --git a/data/38/FF/73/38FF73117E665EDBB5E0412309984A19.xml b/data/38/FF/73/38FF73117E665EDBB5E0412309984A19.xml new file mode 100644 index 00000000000..55dc818e630 --- /dev/null +++ b/data/38/FF/73/38FF73117E665EDBB5E0412309984A19.xml @@ -0,0 +1,720 @@ + + + +Taxonomy, phylogeny, and biodiversity of Lumbrineridae (Annelida, Polychaeta) from the Central Pacific Clarion-Clipperton Zone + + + +Author + +Neal, Lenka +https://orcid.org/0000-0002-3857-8428 +Life Sciences Department, Natural History Museum, London SW 7 5 BD, UK +l.nealova@nhm.ac.uk + + + +Author + +Abrahams, Emily +Life Sciences Department, Natural History Museum, London SW 7 5 BD, UK + + + +Author + +Wiklund, Helena +https://orcid.org/0000-0002-8252-3504 +Life Sciences Department, Natural History Museum, London SW 7 5 BD, UK & Department of Marine Sciences, University of Gothenburg, Box 463, 40530 Gothenburg, Sweden & Gothenburg Global Biodiversity Centre, Box 463, 40530 Gothenburg, Sweden + + + +Author + +Rabone, Muriel +https://orcid.org/0000-0002-8351-2313 +Life Sciences Department, Natural History Museum, London SW 7 5 BD, UK + + + +Author + +Bribiesca-Contreras, Guadalupe +https://orcid.org/0000-0001-8163-8724 +Life Sciences Department, Natural History Museum, London SW 7 5 BD, UK + + + +Author + +Stewart, Eva C. D. +https://orcid.org/0000-0001-8383-5705 +Life Sciences Department, Natural History Museum, London SW 7 5 BD, UK & School of Ocean and Earth Sciences, University of Southampton, Southampton, SO 14 3 ZH, UK + + + +Author + +Dahlgren, Thomas G. +https://orcid.org/0000-0001-6854-2031 +Department of Marine Sciences, University of Gothenburg, Box 463, 40530 Gothenburg, Sweden & Gothenburg Global Biodiversity Centre, Box 463, 40530 Gothenburg, Sweden & NORCE Norwegian Research Centre, Bergen, Norway + + + +Author + +Glover, Adrian G. +https://orcid.org/0000-0002-9489-074X +Life Sciences Department, Natural History Museum, London SW 7 5 BD, UK + +text + + +ZooKeys + + +2023 + +2023-07-25 + + +1172 + + +61 +100 + + + + +http://dx.doi.org/10.3897/zookeys.1172.100483 + +journal article +http://dx.doi.org/10.3897/zookeys.1172.100483 +1313-2970-1172-61 +6BAEC3DEE4B3477B948DDC1E0ACA631B +C30E46C9902F54D6B9BEDAC556A407ED + + + + +Lumbrinerides cf. laubieri (NHM_0020) + + + + +Figs 9A-G +, 10A-I +, 11A-K + + + +Material examined. + +NHM_0020, NHM ANEA 2022.801, coll. +9 Oct. 2013 +, AB01, UK-1, EBS, +13.8372 +, +-116.55843 +, +4336 m +, https://data.nhm.ac.uk/object/cfc84885-578e-4b87-a14f-e8fc1cf2a5a0; NHM_0028, NHM ANEA 2022.802, coll. +9 Oct. 2013 +, AB01, UK-1, EBS, +13.8372 +, +-116.55843 +, +4336 m +, https://data.nhm.ac.uk/object/0adcf12b-4027-4893-98a2-588d60e352a3; NHM_1146, NHM ANEA 2022.803, coll. +26 Feb. 2015 +, AB02, OMS, EBS, +12.1155 +, +-117.1645 +, +4100 m +, https://data.nhm.ac.uk/object/4849b790-53a1-45f8-a7e0-3f60062642cd; NHM_2245, NHM ANEA 2022.805, coll. +1 Mar. 2015 +, AB02, OMS, EBS, +12.25733 +, +-117.30217 +, +4302 m +, https://data.nhm.ac.uk/object/024a6d28-6775-4d01-823b-3b0a03fcd727; NHM_3492, NHM ANEA 2022.804, coll. +1 Mar. 2020 +, RC01, OMS, Box core, +14.03696 +, +-116.50802 +, +4138 m +, https://data.nhm.ac.uk/object/e6b00cf4-5c01-453d-a1ff-5c7dc0783960; NHM_4738_ECDS1, NHM ANEA 2022.808, coll. +28 Feb. 2020 +, RC01, UK-1, Box core, +13.98698 +, +-116.47664 +, +4059 m +, https://data.nhm.ac.uk/object/c78086ef-af8a-4b1c-b9db-e61df25585f4; NHM_4738_ECDS3, NHM ANEA 2022.807, coll. +28 Feb. 2020 +, RC01, UK-1, Box core, +13.98698 +, +-116.47664 +, +4059 m +, https://data.nhm.ac.uk/object/7d7e9048-38fa-4503-b256-6e6ac3c23687; NHM_4738_ECDS5, NHM ANEA 2022.806, coll. +28 Feb. 2020 +, RC01, UK-1, Box core, +13.98698 +, +-116.47664 +, +4059 m +, https://data.nhm.ac.uk/object/2806a25b-e00e-4845-9b6a-10ca95b3fd6a; NHM_4743_ECDS1, NHM ANEA 2022.809, coll. +4 Mar. 2020 +, RC01, UK-1, Box core, +13.99732 +, +-116.52824 +, +4102 m +, https://data.nhm.ac.uk/object/d42c9eb3-2052-4e90-9e00-61e20291d674; NHM_8777_HW01, NHM ANEA 2022.811, coll. +12 Nov. 2020 +, DG05a, NORI-D, Box core, +10.3781 +, +-117.14689 +, +4300 m +, https://data.nhm.ac.uk/object/18c5a2d0-2bd6-48e2-bd02-9fe7c03ae7a4; NHM_8810, NHM ANEA 2022.815, coll. +23 Nov. 2020 +, DG05a, NORI-D, Box core, +10.3554 +, +-117.22087 +, +4289 m +, https://data.nhm.ac.uk/object/75d2356a-cfd2-4ea8-b6d4-7d69ee27cb1c; NHM_8855, NHM ANEA 2022.816, coll. +30 Oct. 2020 +, DG05a, NORI-D, Box core, +10.92904 +, +-116.26351 +, +4262 m +, https://data.nhm.ac.uk/object/2250d689-4b91-4998-8776-05db9d437c89; NHM_8874, NHM ANEA 2022.817, coll. +2 Nov. 2020 +, DG05a, NORI-D, Box core, +10.9714 +, +-116.16494 +, +4240 m +, https://data.nhm.ac.uk/object/4d437d57-72b5-4f7a-84b7-87b13b6c422d; NHM_8898_LN01, NHM ANEA 2022.812, coll. +2 Nov. 2020 +, DG05a, NORI-D, Box core, +10.97448 +, +-116.35427 +, +4260 m +, https://data.nhm.ac.uk/object/af52e52a-9c50-432e-a88c-1f03cb6f981c; NHM_8898_LN02, NHM ANEA 2022.813, coll. +2 Nov. 2020 +, DG05a, NORI-D, Box core, +10.97448 +, +-116.35427 +, +4260 m +, https://data.nhm.ac.uk/object/123e1f28-a76e-4929-9c58-7ffd80db14a2; NHM_8898_LN03, NHM ANEA 2022.814, coll. +2 Nov. 2020 +, DG05a, NORI-D, Box core, +10.97448 +, +-116.35427 +, +4260 m +, https://data.nhm.ac.uk/object/2c462f72-683e-4fb3-bef9-8a8fe10b98f3; NHM_8798_HW02, NHM ANEA 2022.810, coll. +8 Nov. 2020 +, DG05a, NORI-D, Box core, +10.32571 +, +-117.17753 +, +4300 m +, https://data.nhm.ac.uk/object/568f9a43-2c36-49be-8829-55edb69ba271. + + + +Comparative material examined. + +Fig. +12A-I +. + +Lumbrinerides laubieri + +Miura, 1980; + +holotype +MNHN.1278. +NE Atlantic +, +Gulf of Gascogne +, +Biogas IV +, DS61, coll. +24 Feb 1974 +, +24.02.1974 +, +47.5686111 +, +-9.6355556 +, 2 + + +250 m + +. + + + + + +Description. + +All specimens posteriorly incomplete, including voucher specimens NHM_0020, NHM_ 4378_ECDS5, NHM_1146, NHM_2245 and NHM_3492. Body slender, narrow, and cylindrical measuring up to 3.1 mm in length for 11 chaetigers and width of 0.2-0.25 mm. Live specimens iridescent and slightly translucent, with visible spotted pattern along sides of prostomium; preserved specimens milky white in ethanol (Fig. +9A +). Jaws typically visible through body (Fig. +9E +). + + + +Figure 9. +Lumbrinerides cf. laubieri +A +anterior fragment of specimen NHM_1146 in dorsal view +B +simple bidentate hooded hook on chaetiger 3, specimen NHM_1146 +C +winged limbate capillary chaetae on chaetiger 5 specimen, NHM_1146 +D +maxillary apparatus, specimen NHM_1146 E everted jaws in specimen NHM_3492 +F +maxillary apparatus of specimen NHM_1146 (MIII = maxilla 3, MIV = maxilla 4) +G +maxillary apparatus of specimen NHM_2245 (md. = mandibles). Scale bars: 50 +µm +( +C +); 10 +µm +( +B +); 100 +µm +( +D, E, F, G +). Abbreviations: ca. = carriers, MI = maxilla 1, MII = maxilla 2, al = attachment lamellae. + + + + +Figure 10. +Lumbrinerides cf. laubieri +(specimen NHM_ 4378_ECDS5) +A +posteriorly incomplete preserved specimen +B +anterior end with margins between prostomium and 2-rigned peristomium +C +anterior end with margins between prostomium, peristomium and chaetiger 1 +D +chaetigers 2-7 marked by arrows, showing the shift of parapodia from lateral to dorsal position +E +chaetiger 1 +F +chaetiger 2 +G +chaetiger 3 +H +chaetiger 4 with postchaetal lobe +I +chaetigers 5-6 with postchaetal lobes. Scale bars: 250 +µm +( +A, C, D +); 100 +µm +( +B +); 25 +µm +( +F, G, H +); 50 +µm +( +I +). + + + +Prostomium significantly longer than wide (Figs +9A +, +10A +, +11A +), narrow, conical, bluntly pointed, with small papilla at the tip; with spotted pigmentation across length of prostomium. Peristomium with two rings (Fig. +10B, C +), the first with a V-shaped notch on the ventral side. + + + +Figure 11. +Lumbrinerides cf. laubieri +(specimen NHM_0020) +A +posteriorly incomplete preserved specimen +B +parapodia of chaetiger 4 and dorsally shifted parapodia of chaetiger 5, both with developed postchaetal lobes +C +detail of pre- and postchaetal lobes of chaetiger 4 +D +detail of pre- and postchaetal lobes of chaetiger 5 +E +chaetae of chaetiger 1, with limbate chaetae showing broad limbation (elbow) +F +chaetae of chaetiger 2 +G +chaetae of chaetiger 3 +H +chaetae of chaetiger 4 +I +simple hooded hook of chaetiger 4 +J +simple hooded hook of chaetiger 7 +K +narrowly limbate capillary from chaetiger 5. Scale bars: 250 +µm +( +A +); 50 +µm +( +B +); 25 +µm +( +C-K +). + + + +Maxillary apparatus with four pairs of maxillae (Fig. +9D, F +). All maxillae with attachment lamellae. Carriers as long as MI and joined to their entire base (Fig. +9D +). Carriers with wide anterior base and coloured dark brown to black. MI without internal accessory teeth. Attachment lamellae along lateral edge of MI, thin and weakly sclerotised. MII shorter than MI with three rounded teeth. MIII as edentate plate, pigmented dark brown. MIV as edentate plate, appear elongated and slightly pointed, approximately triangular (Fig. +9F +). Mandibles fused for entire length with three pigmented bands (Fig. +9G +). + + +Parapodia reduced to. Chaetigers 1 and 2 distinctly longer than wide, with reduced parapodia, no lobes developed, situated laterally (Fig. +10D, E, F +). Chaetiger 3 ca. as wide as long, with reduced parapodia shifted dorsolaterally, no lobes developed (Fig. +10D, G +). Chaetiger 4 ca. as wide as long with small tongue-like postchaetal lobe (Figs +10D, H +, +11C +), shifted dorsolaterally. From chaetiger 5, chaetigers ca. as wide as long, shifted dorsally, with small tongue-like postchaetal lobes developed (Figs +10D, I +, +11B, D +). Pre-chaetal lobes always smaller than postchaetal lobes. + + +Chaetae of two types observed in all chaetigers: 1. simple bidentate hooded hooks with two teeth at ~ 45° from each other, with subdistal spur, 1-3 hooks per parapodium, usually two present (Figs +9B +, +11I, J +) and two winged limbate capillaries (Fig. +9C +), usually two per parapodium; in chaetiger 1-4 capillaries broadly limbate (with elbow) (Fig. +11E-H +), from chaetiger 5 narrowly limbate (Figs +9C +, +11K +). Aciculae yellow. Remainder of body and pygidium unknown. + + + +Genetic data. + +In our phylogenetic analysis, +Lumbrinerides cf. laubieri +(NHM_0020) forms a well-supported monophyletic clade with another, as yet unnamed + +Lumbrinerides + +species (Fig. +3 +). + + +There are many identical or near-identical COI matches to unnamed specimens on GenBank that were previously collected at the CCZ ( +Janssen et al. 2015 +, +2019 +). There are no genetic data from the type or non-type specimens of + +Lumbrinerides laubieri + +. + + + +Remarks. + +This small species was the most abundant lumbrinerid in our CCZ samples, represented by 211 specimens. Morphologically, this species is similar to + +Lumbrinerides laubieri + +Miura, 1980, described from the Gulf of Gascony, France at lower bathyal depths of 1894-2775 m. Outside its type locality, + +L. laubieri + +has been reported in the North Aegean Sea at 156-300 m ( +Simboura and Zenetos 2005 +). Following the initial examination of CCZ specimens, these matched + +L. laubieri + +in several instances: small body size; greatly elongated prostomium; reduced parapodia in first three chaetigers; maxillae I without accessory teeth; mandibles with "concentric striations" consistent with the coloured bands seen on CCZ specimens (Fig. +9G +); attachment lamellae supporting the maxillary apparatus present (Fig. +9D +); two types of chaetae present, limbate capillary chaetae and simple bidentate hooded hooks (Fig. +9B, C +). + + +The holotype MNHN.1278 of + +L. laubieri + +was re-examined as part of this study (Fig. +12A-I +). The holotype is a small, very slender specimen, consisting of three fragments: the anterior fragment with 15 chaetigers being 4.5 mm long and 0.25 mm wide (Fig. +12A, B +), a body fragment with six chaetigers, and a small 2-chaetiger long body fragment. The jaws were partially damaged during a previous investigation. Chaetae (particularly the limbate type) were often broken off. + + + +Figure 12. + +Lumbrinerides laubieri + +, holotype MNHN.1278 +A, B +preserved specimen in dorsal view +C +chaetiger 1 +D, E +chaetiger 4 with postchaetal lobe +F +postchaetal lobe from chaetiger 10 +G +broadly limbate chaetae from chaetiger 1 +H, I +hooded hooks, with inserts showing the detail of bidentate dentition. Scale bars: 1 mm ( +A, B +); 250 +µm +( +C, F G, H, I +); 500 +µm +( +D, E +). + + + +In a recent revision of + +Lumbrinerides + +from Japanese water, +Miura (2017) +suggested new characters of taxonomic importance in this genus. Therefore, during the examination of type material particular attention has been paid to the following characters: the chaetiger on which the first hooks arise, the number of hooks per parapodium and the number of anterior reduced parapodia. No obvious differences were observed (Table +2 +), other than the presence of up to three hooks in some parapodia in CCZ specimens, while at most two were observed in the holotype of + +L. laubieri + +. However, other more subtle differences were observed that are usually not considered in the discussion of the taxonomic characters in +Lumbrineridae +. These differences refer to relative size of various features, unlikely to be related to size of specimen as all individuals investigated had small and very slender body of similar dimensions. The hooded hooks in CCZ specimens are very small and slender, with dentition only clearly observable under oil (x100 magnification), while the hooks in + +L. laubieri + +are much chunkier and easy to observe even under lower magnification ( +x +40) (Fig. +12H, I +). Similarly, the development of broad limbation (elbow) on capillaries of anterior chaetigers is much more distinct in + +L. laubieri + +(Fig. +12C, G +) compared to CCZ specimens (Fig. +12E +). Characters discussed by +Miura (2017) +or in this study are summarised in Table +2 +. + + + +Table 2. +Comparison of selected characters of + +L. laubieri + +and CCZ specimens. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
CharacterHolotype MNHN.1278CCZ specimens
chaetiger on which the first hooks arise11
the number of hooks per chaetiger1-21-3 (mostly 2)
dentition of the bidentate hook +chunky (easily observed under +x +40 mag); teeth separated by ~ 90° + +slender (need to be observed under +x +100 mag); teeth separated by ~ 45° +
the number of limbate chaetae per chaetiger2?1-2
limbate chaetae of anteriormost chaetigersbroad elbow well developedbroad elbow less developed
the number of chaetigers with reduced parapodia (=no lobes developed)1-31-3
parapodia inserted laterallyon ch. 1-2on ch. 1-2
parapodia with dorsolateral position?ch 3-4
parapodia inserted dorsallyfrom chaetiger 5from chaetiger 5
+
+ +Lastly, a bathymetric distributional pattern should be also taken into consideration as + +L. laubieri + +has been found in shallower depth (1894-2775 m) in the Atlantic, compared to CCZ specimens (~ 5000 m) in the Pacific. Depth is considered to be a greater barrier to gene flow compared to with horizontal distances (e.g., Atlantic vs. Pacific) ( +Taylor and Roterman 2017 +). Unfortunately, molecular data from + +L. laubieri + +is not available for comparison. Thus, it is currently difficult to establish the new species based on CCZ specimens, and these are cautiously ascribed to +Lumbrinerides cf. laubieri +Miura, 1980. + + +Two more + +Lumbrinerides + +species have a conical, greatly elongated prostomium: + +Lumbrinerides carpinei + +(Ramos, 1976) described from Mediterranean Sea (off Monaco, at depths of 200-600 m) and + +Lumbrinerides yoshioi + +Miura, 2017 from shallow depths off Hokkaido, Japan. However, they have the following differences from CCZ specimens. + +Lumbrinerides carpinei + +has one long apodous segment rather than two peristomial rings, lacks visible mandibles and has accessory tooth on MI ( +Miura 1980 +). + +Lumbrinerides yoshioi + +differs in having 9-10 reduced anterior parapodia (as opposed to 3 in CCZ specimens) and in MI having two weakly projected accessory teeth (as opposed to no accessory teeth in CCZ specimens). + +
+ +Distribution. + +Central Pacific Ocean, Eastern CCZ, found in +'UK-1' +, +'OMS' +and +'NORI-D' +exploratory areas (Fig. +1 +). + + +
+
\ No newline at end of file diff --git a/data/38/FF/A7/38FFA70E5FC11D6FB5798CAC175E2774.xml b/data/38/FF/A7/38FFA70E5FC11D6FB5798CAC175E2774.xml new file mode 100644 index 00000000000..e8087c03c54 --- /dev/null +++ b/data/38/FF/A7/38FFA70E5FC11D6FB5798CAC175E2774.xml @@ -0,0 +1,58 @@ + + + +Checklist of British and Irish Hymenoptera - Platygastroidea + + + +Author + +Buhl, Peter N. + + + +Author + +Broad, Gavin R. + + + +Author + +Notton, David G. + +text + + +Biodiversity Data Journal + + +2016 + +4 + + +7991 +7991 + + + + +http://dx.doi.org/10.3897/BDJ.4.e7991 + +journal article +http://dx.doi.org/10.3897/BDJ.4.e7991 +1314-2828-4-7991 + + + + +Platygaster (Platygaster) herricki Packard, 1841 + + + +Distribution +England + + + \ No newline at end of file diff --git a/data/38/FF/C6/38FFC61053BF50CEAC9310E49FFAD9C4.xml b/data/38/FF/C6/38FFC61053BF50CEAC9310E49FFAD9C4.xml new file mode 100644 index 00000000000..d51fb82926b --- /dev/null +++ b/data/38/FF/C6/38FFC61053BF50CEAC9310E49FFAD9C4.xml @@ -0,0 +1,104 @@ + + + +Psychodidae (Diptera) of Azerbaijan and Georgia - faunistics with biodiversity notes + + + +Author + +Jezek, Jan +Department of Entomology, National Museum, Cirkusova 1740, CZ - 193 00 Praha 9 - Horni Pocernice, Czech Republic + + + +Author + +Manko, Peter +https://orcid.org/0000-0003-1862-9117 +Department of Ecology, Faculty of Humanities and Natural Sciences, University of Presov, 17. novembra 1, SK - 081 16 Presov, Slovakia +peter.manko@unipo.sk + + + +Author + +Obona, Jozef +https://orcid.org/0000-0002-1185-658X +Department of Ecology, Faculty of Humanities and Natural Sciences, University of Presov, 17. novembra 1, SK - 081 16 Presov, Slovakia + +text + + +ZooKeys + + +2021 + +2021-06-15 + + +1049 + + +15 +42 + + + + +http://dx.doi.org/10.3897/zookeys.1049.66063 + +journal article +http://dx.doi.org/10.3897/zookeys.1049.66063 +1313-2970-1049-15 +E0AEB4DB6C32407697542AA74386C517 +F43B77514DD55AC69BA1E334AE61ABF2 + + + + +Tinearia alternata (Say, 1824) + + + +Material examined. + + + +Georgia + +: G 03, +27.9.2019 +, +1♀ +, slide +Inv. No. +25603, leg. PM; G 08 + +, +1.5.2019 +, +1♀ +, slide Inv. No. 25683, leg. JO; g 56, +26.4.2019 +, +1♀ +, slide Inv. No. 25682, leg. JO. + + + +Distribution. + +Cosmopolitan and euryvalent species ( + +Kroca +and +Jezek +2019 + +). + + + + \ No newline at end of file diff --git a/data/38/FF/F3/38FFF3FF3B675D52B57E14B088C6BE36.xml b/data/38/FF/F3/38FFF3FF3B675D52B57E14B088C6BE36.xml new file mode 100644 index 00000000000..53bbb4c370e --- /dev/null +++ b/data/38/FF/F3/38FFF3FF3B675D52B57E14B088C6BE36.xml @@ -0,0 +1,100 @@ + + + +Taxonomic changes in Oenothera sections Gaura and Calylophus (Onagraceae) + + + +Author + +Wagner, Warren L. +Department of Botany, MRC- 166, National Museum of Natural History, Smithsonian Institution, P. O. Box 37012, Washington, DC 20013 - 7012, USA +wagnerw@si.edu + + + +Author + +Krakos, Kyra N. +Biology Department, Maryville University, 650 Maryville University Dr., St. Louis, MO 63141, USA + + + +Author + +Hoch, Peter C. +Missouri Botanical Garden, P. O. Box 299, St. Louis, MO 63166 - 0299, USA + +text + + +PhytoKeys + + +2013 + +2013-11-04 + + +28 + + +61 +72 + + + + +http://dx.doi.org/10.3897/phytokeys.28.6143 + +journal article +http://dx.doi.org/10.3897/phytokeys.28.6143 +1314-2003-28-61 +FFBCE22D163DFF8AFF8EFF954A44FF90 +576178 + + + + + +6. +Oenothera hexandra (Ortega) W. L. Wagner & Hoch, Syst. Bot Monogr. 83: 212. 2007. + + + +Basionym. + + +Gaura hexandra + +Ortega, Hort. matr. dec. 14. 1797. + + + +Type. + +Based on living plants cultivated at the Royal Botanical Garden in Madrid from seeds sent by +Sesse +from Mexico [erroneously said to be from Cuba] (Holotype: not located).-Mexico. +Mexico +. Comunidad Temascaltepec, 19 May 1936, G. B. Hin +ton +7688 (Neotype, designated, by +Wagner et al. 2007 +: 212: MO-1717467!; Isoneotypes: C, F, G, GH, LL, MICH, NY, US!). + + +Annual herb from a stout taproot, usually well-branched at the base and above, 15-100 cm tall, villous proximally, the leaves subglabrous to densely short-villous, and becoming subglabrous, strigillose, and/or glandular-puberulent distally. Leaves in a basal rosette and cauline; rosette leaves lyrate, gradually narrowed to the petiole, usually quickly deciduous; cauline leaves 1-9 +x +0.1-0.8 cm, linear to very narrowly elliptic or narrowly lanceolate, margin sinuate-dentate to subentire, subsessile. Inflorescence strict to somewhat branched, 7-53 cm long, bracts 2-5 cm long, narrowly lanceolate to ovate. Flowers 3-merous, opening at sunset; floral tube 4.5-7.5 mm; sepals 3-10 mm; petals 4.5-7 mm; staminal filaments 3-6 mm, anthers 1-2 mm, pollen 90-100% fertile; style 9-14.5 mm. Capsule indehiscent, 4.5-8 +x +2-4.5 mm, nut-like, hard, woody, not reflexed, the body ellipsoid or narrowly obovoid, broadly winged on the angles and deeply furrowed between the angles, narrowed at the base but not stipitate. Seeds 3, 1.75-3 mm, ovoid, usually flattened on one or several sides by crowding in the fruit, yellowish to reddish brown. Gametic chromosome number: n = 7. Self-compatible and highly autogamous. + + + +Phenology and distribution. +Flowering from March to November. From Durango, Mexico south in the Sierra Madre Occidental to the Trans Mexican Volcanic Belt, where abundant, and in Chiapas, Mexico as well as Guatemala in grasslands, meadows or oak woodlands, or disturbed areas, in sandy soils; 1800-2430 m. + + + + \ No newline at end of file