From 3ebc41b19cdd1a81518a64c70adbc6e2fef32704 Mon Sep 17 00:00:00 2001 From: ggserver Date: Thu, 9 Jan 2025 18:35:13 +0000 Subject: [PATCH] Add updates up until 2025-01-09 18:29:08 --- .../87/038B87B1FFF0023900CC8F4FFAD1065B.xml | 92 ++- .../87/038B87B1FFF80238027B8CB8FE9F04AC.xml | 388 +++++---- .../87/03DA87BEFFA3FFD907F2EC52766F4626.xml | 592 ++++++++++++++ .../87/03DA87BEFFA7FFD407F2EC60769A426A.xml | 626 +++++++++++++++ .../8D/17378D71DA3D5C7A8255B768107F116B.xml | 116 +++ .../EB/3668EB2BE84E53D989C67C09FC656247.xml | 298 +++++++ .../88/391D8874F1485D67B6E6E652389517BB.xml | 223 ++++++ .../C4/3B05C4F631AD50F7B51A9B5596DE560E.xml | 439 ++++++++++ .../00/451E00DA591F584F85A241FC1F6834CC.xml | 347 ++++++++ .../C7/471DC710F3595A73875832F3C4581E23.xml | 753 ++++++++++++++++++ .../3E/52FC3E3F8F3D51739C8D1A6378DC38C6.xml | 327 ++++++++ .../E5/69FBE51B451C57A88F21584882A89FC7.xml | 393 +++++++++ .../24/831524D8E34E5890B8622D92AB730445.xml | 426 ++++++++++ .../59/A46C5981898F53AFA9BA5002BB19AC85.xml | 317 ++++++++ .../74/AC7C741F6FBB5CE884AFFC6BEB07096E.xml | 131 +++ .../65/AD6365B292675E2AB330779926A0ACEC.xml | 123 +++ .../5D/CB1B5D206DA25D84B9D4EBA6F558C1CB.xml | 114 +++ .../8C/D7178C0065385A48BF28E24F28153231.xml | 275 +++++++ .../0A/FB7F0A266D625ECEBE3EC29C56C9E0FF.xml | 277 +++++++ 19 files changed, 6066 insertions(+), 191 deletions(-) create mode 100644 data/03/DA/87/03DA87BEFFA3FFD907F2EC52766F4626.xml create mode 100644 data/03/DA/87/03DA87BEFFA7FFD407F2EC60769A426A.xml create mode 100644 data/17/37/8D/17378D71DA3D5C7A8255B768107F116B.xml create mode 100644 data/36/68/EB/3668EB2BE84E53D989C67C09FC656247.xml create mode 100644 data/39/1D/88/391D8874F1485D67B6E6E652389517BB.xml create mode 100644 data/3B/05/C4/3B05C4F631AD50F7B51A9B5596DE560E.xml create mode 100644 data/45/1E/00/451E00DA591F584F85A241FC1F6834CC.xml create mode 100644 data/47/1D/C7/471DC710F3595A73875832F3C4581E23.xml create mode 100644 data/52/FC/3E/52FC3E3F8F3D51739C8D1A6378DC38C6.xml create mode 100644 data/69/FB/E5/69FBE51B451C57A88F21584882A89FC7.xml create mode 100644 data/83/15/24/831524D8E34E5890B8622D92AB730445.xml create mode 100644 data/A4/6C/59/A46C5981898F53AFA9BA5002BB19AC85.xml create mode 100644 data/AC/7C/74/AC7C741F6FBB5CE884AFFC6BEB07096E.xml create mode 100644 data/AD/63/65/AD6365B292675E2AB330779926A0ACEC.xml create mode 100644 data/CB/1B/5D/CB1B5D206DA25D84B9D4EBA6F558C1CB.xml create mode 100644 data/D7/17/8C/D7178C0065385A48BF28E24F28153231.xml create mode 100644 data/FB/7F/0A/FB7F0A266D625ECEBE3EC29C56C9E0FF.xml diff --git a/data/03/8B/87/038B87B1FFF0023900CC8F4FFAD1065B.xml b/data/03/8B/87/038B87B1FFF0023900CC8F4FFAD1065B.xml index e7fe92e7609..9cd49b3341f 100644 --- a/data/03/8B/87/038B87B1FFF0023900CC8F4FFAD1065B.xml +++ b/data/03/8B/87/038B87B1FFF0023900CC8F4FFAD1065B.xml @@ -1,69 +1,73 @@ - - - -New genus of subfamily Cypridopsinae Kaufmann, 1933 (Crustacea: Ostracoda) from Thailand + + + +New genus of subfamily Cypridopsinae Kaufmann, 1933 (Crustacea: Ostracoda) from Thailand - - -Author + + +Author -Savatenalinton, Sukonthip +Savatenalinton, Sukonthip -text - - -European Journal of Taxonomy +text + + +European Journal of Taxonomy - -2018 - -2018-12-17 + +2018 + +2018-12-17 - -487 + +487 - -1 -17 + +1 +17 -journal article -28584 -10.5852/ejt.2018.487 -065bf0fe-9b66-4860-9865-c4fdcce67077 -2552713 -B66E895B-C8AA-4E12-B4A7-11907E72D478 +journal article +10.5852/ejt.2018.487 +065bf0fe-9b66-4860-9865-c4fdcce67077 +2118-9773 +2552713 +B66E895B-C8AA-4E12-B4A7-11907E72D478 - + Key to genera with LV overlapping RV in the subfamily -Cypridopsinae +Cypridopsinae - + 1. Respiratory plate of T1 absent ................................................... Austrocypridopsis McKenzie, 1982 - -– Respiratory plate of T1 present ......................................................................................................... 2 + + +– Respiratory plate of T1 present ......................................................................................................... 2 + - -2. Claw G2 on A2 strongly serrated ...................................................................................................... 3 -– Claw G2 on A2 normal developed .................................................................................................... 5 - + +2. Claw G2 on A2 strongly serrated ...................................................................................................... 3 + + +– Claw G2 on A2 normal developed .................................................................................................... 5 + @@ -100,28 +104,32 @@ McKenzie, 1982 - + 5. Pincer organ on T3 absent ........................................................................ Neocypridopsis Klie, 1940 - -– Pincer organ on T3 present ............................................................................................................... 6 + + +– Pincer organ on T3 present ............................................................................................................... 6 + - + 6. CR absent in female and male .................................................. Pseudocypridopsis Karanovic, 1999 - -– CR present in female ........................................................................................................................ 7 + + +– CR present in female ........................................................................................................................ 7 + diff --git a/data/03/8B/87/038B87B1FFF80238027B8CB8FE9F04AC.xml b/data/03/8B/87/038B87B1FFF80238027B8CB8FE9F04AC.xml index 9fdb203d71c..fd8651adc2d 100644 --- a/data/03/8B/87/038B87B1FFF80238027B8CB8FE9F04AC.xml +++ b/data/03/8B/87/038B87B1FFF80238027B8CB8FE9F04AC.xml @@ -1,42 +1,42 @@ - - - -New genus of subfamily Cypridopsinae Kaufmann, 1933 (Crustacea: Ostracoda) from Thailand + + + +New genus of subfamily Cypridopsinae Kaufmann, 1933 (Crustacea: Ostracoda) from Thailand - - -Author + + +Author -Savatenalinton, Sukonthip +Savatenalinton, Sukonthip -text - - -European Journal of Taxonomy +text + + +European Journal of Taxonomy - -2018 - -2018-12-17 + +2018 + +2018-12-17 - -487 + +487 - -1 -17 + +1 +17 -journal article -28584 -10.5852/ejt.2018.487 -065bf0fe-9b66-4860-9865-c4fdcce67077 -2552713 -B66E895B-C8AA-4E12-B4A7-11907E72D478 +journal article +10.5852/ejt.2018.487 +065bf0fe-9b66-4860-9865-c4fdcce67077 +2118-9773 +2552713 +B66E895B-C8AA-4E12-B4A7-11907E72D478 - - + + @@ -47,16 +47,16 @@ + + urn:lsid:zoobank.org:act: 8C42600E-3232-40EF-BC77-765E1CC15953 - - -Figs 1–4 +Figs 1–4 @@ -67,13 +67,10 @@ urn:lsid:zoobank.org:act: The specific epithet ‘longispinosa’ refers to the outstanding appearance of long spines on valve surface. This is the most prominent character of the new species and can be easily recognized from external morphology. - + - -Type -material - +Type material @@ -82,7 +79,7 @@ material - + THAILAND – @@ -90,20 +87,22 @@ material (NE) • -♀ +♀ (soft parts dissected in glycerine on a sealed glass slide and valves stored dry on a micropalaeontological slide); -Huai Jorakae Mak -(reservoir), -Muang district -; 14°54΄41˝ -N -, 103°03΄07˝ -E +Huai Jorakae Mak (reservoir) +, +Muang district +; +14°54΄41˝ N +, +103°03΄07˝ E ; 4 Oct. 2010 -; MSU-ZOC.257. +; +MSU-ZOC.257 +. @@ -112,77 +111,72 @@ material - + THAILAND – Buriram Province (NE) - • - -3 ♀♀ -(stored as the -holotype -); same locality as for holotype; +3 ♀♀ +(stored as the holotype); same locality as for holotype; 4 Oct. 2010 -; MSU-ZOC.258, 261 to 262 +; +MSU-ZOC.258 +, 261 to 262 • - -2 ♀♀ -(stored as the -holotype -); -Kwan -Phayao + +2 ♀♀ +(stored as the holotype); +Kwan Phayao (lake); 6 Oct. 2007 -; MSU-ZOC.263 to 264 +; +MSU-ZOC.263 to 264 • - -2 ♀♀ + +2 ♀♀ (carapaces stored dry on micropalaeontological slides); same locality as for holotype; 4 Oct. 2007 ; -MSU -.ZOC.259 to 260 +MSU.ZOC.259 +to 260 • - -1 ♀ + +1 ♀ (carapace stored dry on micropalaeontological slide); -Kwan -Phayao +Kwan Phayao (lake); 6 Oct. 2007 ; -MSU -.ZOC.265 +MSU.ZOC.265 • - -9 ♀♀ + +9 ♀♀ (in 70% ethanol); same locality as for holotype; 4 Oct. 2010 ; -MSU -.ZOC.266 +MSU.ZOC.266 . + + Type @@ -303,6 +297,7 @@ sp., . + Fig. 1. @@ -335,13 +330,14 @@ Anterior part of RVi (idem). Posterior part of RVi (idem). Scale bars: A–C, F–G = 100 µm; D, L = 10 µm; E = 13 µm; H–K = 58 µm. + Other material examined - + THAILAND – @@ -354,132 +350,213 @@ Posterior part of RVi (idem). Scale bars: A–C, F–G = 100 µm; D, L = 10 µm; 7 ♀♀ ; locality 1; Kwan -Phayao +Phayao (lake), Muang District -; -19°09΄33˝ N -, -99°54΄36˝ E -; +; 19°09΄33˝ N, 99°54΄36˝ E; 6 Oct. 2007 ; accompanying ostracod fauna: -Astenocypris papyracea -(Sars, 1903) + +Astenocypris +papyracea + +( +Sars +, 1903) , -Bradleystrandesia weberi + +Bradleystrandesia +weberi + , -Bradleytriebella lineata -, -Cypretta - -sp., - -Cypridopsis vidua -, Cypridopsine + +Bradleytriebella +lineata -sp., +, + +Cypretta + + +sp. +, + + +Cypridopsis +vidua + +, +Cypridopsine + +sp. +, + Cypris subglobosa -Sowerby, 1840 +Sowerby + +, 1840 , + Dentocypria smithi Savatenalinton, 2017 + , -Pseudostrandesia calapanensis -(Tressler, 1937) + +Pseudostrandesia +calapanensis + +( +Tressler +, 1937) , -Pseudostrandesia mamarilorum + +Pseudostrandesia +mamarilorum + , + Stenocypris - malayaica -Victor & Fernando, 1981, +Victor & Fernando + + +, 1981, -Strandesia kraepelini + +Strandesia +kraepelini + , + Tanycypris siamensis -Savatenalinton & Martens, 2009 +Savatenalinton & Martens + +, 2009 ; TH142 . – -Roi-Et Province (NE) + +Roi-Et Province +( +NE +) + • -19 ♀♀ -; locality 2; Lam Phayom (reservoir); 16°17΄17˝ N, 103°59΄46˝ E; +19 ♀♀ +; locality 2; +Lam Phayom +(reservoir); 16°17΄17˝ N, 103°59΄46˝ E; 25 Oct. and 20 Feb. 2010 ; accompanying ostracod fauna: -Bradleystrandesia weberi + +Bradleystrandesia +weberi + , -Bradleytriebella lineata -, Cypridopsine + +Bradleytriebella +lineata + +, +Cypridopsine -sp., +sp. +, -Dentocypria aequiloba + +Dentocypria +aequiloba + , -Dentocypria chantaranothaii + +Dentocypria +chantaranothaii + , -Limnocythere + +Limnocythere + -sp., +sp. +, -Pseudocypretta maculata + +Pseudocypretta +maculata + , + Pseudostrandesia thailandensis -Savatenalinton & Martens, 2010 +Savatenalinton & Martens + +, 2010 , + Stenocypris derupta -Vávra, 1906, +Vávra + +, 1906, -Strandesia kraepelini + +Strandesia +kraepelini + , + Strandesia sexpunctata -Klie, 1932 +Klie + +, 1932 , -Strandesia + +Strandesia + -sp.; NE067. – +sp. +; NE067. – Chaiyaphum Province -(NE) +( +NE +) • -5 ♀♀ +5 ♀♀ ; locality 3; Nong PagPung (swamp), Phu Kiew District; 16°22΄27˝ N, 102°08΄02˝ E; 30 Oct. 2010 ; accompanying ostracod fauna: @@ -507,10 +584,12 @@ sp., Chaiyaphum Province -(NE) +( +NE +) • -2 ♀♀ +2 ♀♀ ; locality 4; Nong Sammuen (swamp), Phu Kiew District; 16°24΄27˝ N, 102°02΄02˝ E; 30 Oct. 2010 ; accompanying ostracod fauna: @@ -552,10 +631,12 @@ sp., Chaiyaphum Province -(NE) +( +NE +) • -2 ♀♀ +2 ♀♀ ; locality 5; Lam Nam Kam (rivulet), Muang; 15°46΄37˝ N, 102°13΄18˝ E; 3 Oct. 2010 ; accompanying ostracod fauna: @@ -607,10 +688,12 @@ Savatenalinton & Martens, 2010 Chaiyaphum Province -(NE) +( +NE +) • -2 ♀♀ +2 ♀♀ ; locality 6; Huai Pao (river), Kaset Sombun District, 16°23΄03˝ N, 101°58΄47˝ E; 9 Oct. 2007 ; accompanying ostracod fauna: @@ -654,10 +737,12 @@ Klie, 1932 Ubon Ratchathani Province -(NE) +( +NE +) • -2 ♀♀ +2 ♀♀ ; locality 7; Kang Sapue (river), Phiboon Mangsahan District; 15°14΄37˝ N, 105°14΄37˝ E; 24 Oct. 2010 ; accompanying ostracod fauna: @@ -690,10 +775,12 @@ sp., Cypridopsine sp., Buriram Province -(NE) +( +NE +) • -2 ♀♀ +2 ♀♀ ; locality 8; Chon Pratan Reservoir, Lampaimas District; 15°01΄05˝ N, 102°50΄29˝ E; 8 Feb. 2011 ; accompanying ostracod fauna: @@ -720,10 +807,12 @@ sp., Udon Thani Province -(NE) +( +NE +) • -2 ♀♀ +2 ♀♀ ; locality 9; Nong Kae (swamp), Muang district; 17°27΄59˝ N, 102°48΄39˝ E; 31 Jan. 2011 ; accompanying ostracod fauna: @@ -785,10 +874,12 @@ sp., Udon Thani Province -(NE) +( +NE +) • -2 ♀♀ +2 ♀♀ ; locality 10; Huai Luang (reservoir), Muang district; 17°28΄20˝ N, 102°49΄12˝ E; 31 Jan. 2011 ; accompanying ostracod fauna: @@ -822,10 +913,12 @@ sp. 2, Mukdahan Province -(NE) +( +NE +) • -10 ♀♀ +10 ♀♀ ; locality 11; Nong Lom (swamp), Don Tan District; 16°24΄18˝ N, 104°51΄30˝ E; 19 Dec. 2011 ; accompanying ostracod fauna: @@ -891,7 +984,7 @@ Claw G2 of A2 (idem). Md-palp (MSU-ZOC.263). Scale bars: 50 µm. - + Diagnosis @@ -903,8 +996,6 @@ Md-palp (MSU-ZOC.263). Scale bars: 50 µm. Differential diagnosis - - As @@ -980,7 +1071,7 @@ RVI ( Fig. 1E, G, J–L ). Both anterior and posterior margins subequally rounded, ventral margin sinuous at mid-length, submarginal selvage anteriorly, anterior calcified inner lamella wide, posterior calcified inner lamella narrow with two inner lists, postero-ventral part with c.18–20 prominent tubercles. - + Fig. 3. @@ -991,7 +1082,7 @@ RVI ( A. Md-coxa (MSU-ZOC.257). B. -Mx-1 (MSU- ZOC.264). +Mx-1 (MSU-ZOC.264). C. T1 (idem). D. @@ -1032,14 +1123,13 @@ MD- PALP ( ). First segment with two large setae (S1 and S2), one long and slender seta, and a short, smooth α-seta. Second segment dorsally with three unequal long apical setae, shortest seta reaching tip of next segment; ventrally with group of three long hirsute setae, one shorter hirsute seta and plumose, cone-shaped β-seta with pointed tip. Penultimate segment consisting of three groups of setae: dorsally with group of four unequal, long, subapical setae; laterally with apical γ-seta and three further apical smooth setae, the former slightly plumose (length c. 2.4 times of terminal segment); ventrally with two subapical setae, one long (reaching beyond tip of terminal segment), one short (c. half of terminal segment). Terminal segment bearing three claws and two shorter setae, largest claw appearing strongly robust with hairy ending. -MX -1 ( -Fig. 3B +MX1 ( +Fig. 3B ). With two-segmented palp, basal segment of palp dorsally with group of six long, unequal apical setae; ventrally with one long subapical seta (reaching slightly beyond tip of terminal segment). Terminal segment elongated (length c. 2 times of width), apically with three claws and two setae. Large bristles on endites claw-like, with hirsute ending and spatula-shaped apex, number of large bristles on first to third endites being 1, 1, 2, respectively. Sideways-directed bristles on first endite short, subequal in length. T1 ( -Fig. 3C–D +Fig. 3C–D ). Protopodite with two unequally short a-setae, b-, c- and d-setae absent, distally with 12 hirsute apical setae of unequal length. Endopodite weakly built palp with one very long, hirsute seta and two unequally shorter apical setae, length of shortest one less than ¼ of long one. diff --git a/data/03/DA/87/03DA87BEFFA3FFD907F2EC52766F4626.xml b/data/03/DA/87/03DA87BEFFA3FFD907F2EC52766F4626.xml new file mode 100644 index 00000000000..0df6909a90d --- /dev/null +++ b/data/03/DA/87/03DA87BEFFA3FFD907F2EC52766F4626.xml @@ -0,0 +1,592 @@ + + + +A new species of Mimosa (Leguminosae, ser. Piresianae) from the Brazilian Midwest + + + +Author + +Nogueira, Luan H. P. +0009-0002-3108-262X +Programa de Pós-graduação em Biologia Vegetal, Instituto de Biociências, Universidade Federal de Mato Grosso do Sul, Avenida Senador Felinto Muller, s. n., Cidade Universitária, Campo Grande, Mato Grosso do Sul, 79070 - 900, Brazil +luanhpnogueira@gmail.com + + + +Author + +Morales, Matías +0000-0001-5540-9725 +Instituto de Recursos Biológicos (IRB), Instituto Nacional de Tecnología Agropecuaria (INTA), Los Reseros y N. Repetto, s / n, Hurlingham, Buenos Aires, Argentina & Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Godoy Cruz 2290, CABA, Argentina +mmorales0007@gmail.com + + + +Author + +Sartori, Ângela L. B. +0000-0002-5911-8797 +Laboratório de Sistemática Vegetal, Instituto de Biociências, Universidade Federal de Mato Grosso do Sul, Avenida Senador Felinto Muller, s. n., Cidade Universitária, Campo Grande, Mato Grosso do Sul, 79070 - 90, Brazil +albsartori@gmail.com + +text + + +Phytotaxa + + +2024 + +2024-08-06 + + +662 + + +1 + + +80 +92 + + + + +https://doi.org/10.11646/phytotaxa.662.1.6 + +journal article +307355 +10.11646/phytotaxa.662.1.6 +912b9bbd-fda4-482a-9373-8197a26613e4 +1179-3163 +14516570 + + + + + +Mimosa amolariensis +L.H.P.Nogueira, A.L.B.Sartori & M.Morales + + +sp. nov. + + + + + +Type:— + +Brazil +. +Mato Grosso do Sul +: +Corumbá +, +Serra do Amolar +, +Fazenda Morro Alegre +, +18°01’24.28”S +, +57°31’46.90”W +, + +496 m + +, + +26 July 2023 + +(fl. and fr.), + +LHP Nogueira + +291 ( +holotype +: +CGMS +!) + +. ( +Figs. 1–5 +) + + + + + +Mimosa amolariensis + +can be differentiated from + +M. aguapeia +Barneby + +by the poorly developed venation (versus robust venation), non-anastomosing secondary veins (versus anastomosing secondary veins), and truncate calyx lobes (versus triangular calyx lobes). + + +Subshrub or erect shrub, +1–2 m +tall. Subshrub or erect shrub, +1–2 m +tall. Horizontal underground structures, the primary and old roots ligneous, the secondary roots brown, with brownish-orange lenticels, and inside cream-orange. Branches with filiform, setiform-barbellate, and glandular-setiform trichomes. Aculei absent. Stipules persistent, (3.95–)6.1–12 × +1.4–3.1 mm +, base truncated, apex acute-attenuated, 6–10-nerved; glabrous abaxial surface, pubescent filiform, dense setiform-barbellate and granular trichomes on the adaxial side. Cylindrical petiole, 22.1–45.15(–48.9) mm, pubescent filiform, dense setiform-barbellate, granular and occasionally glandular-setiform trichomes. Rachis 49.2–124.3(–140) mm, pubescent filiform, dense setiform-barbellate and rare glandular-setiform trichomes; spicule absent. Pinnae (4–)5–9(–14) of pairs; petiole +2.5–3.9 mm +, pubescent filiform, dense setiform-barbellate and rare glandular-setiform trichomes; paraphyllidia present. Rachilla (21–)24.6–105(–115.5) mm, pubescent filiform, dense setiform-barbellate trichomes. Leaflets (5–)17–35 jugae; pulvinule with adpressed setiform trichomes; blade 8–21.45 × +2.6–8.2 mm +, elliptical-oblong, base oblique, apex acuminate; 4–5-nerved, secondary veins not anastomosed; glabrous or with adpressed filiform and setiform-barbellate trichomes on both sides; the margin ciliated filiform, setiform-barbellate and rare glandular-setiform trichomes. Synflorescence in terminal panicle or raceme. Inflorescence capitula, prior to anthesis conelike; peduncle +12.1–32.3 mm +, dense pubescent filiform, setiform-barbellate and occasionally glandular-setiform trichomes. Flowers subsessile, tetramerous, with staminate flowers concentrated at the base and perfect flowers in most of the inflorescence; calyx pappiform, (1.7–) +2.95–3.5 mm +, reaching just over half of the corolla, lobes truncated with long-setiform ciliated trichomes; corolla trumpet-shape, +3.3–5.45 mm +, 1-nerved, lobes with long-adpressed trichomes; androecium with pink-white styles, diplostemonous; gynoecium stipitate, oblongobovate, trichomes dense glandular-capitate and granular. Articulated craspedia, 37.2–66.15 × +8.7–9.55 mm +, chestnutbrown, trichomes pubescent filiform, adpressed setiform and dense glandular-setiform, 4–9 articles. Seeds obovatewidely depressed ovate, copper-brown, pleurogram apical-basal. + + + +FIGURE 1. + +Mimosa amolariensis + +. A. Flowering branch. B. Stipule. C. Leaflet, adaxial surface; D. Leaflet, abaxial surface. E. Flower. F. Ovary. G. Fruits. H. Seed. A–B and G–H +A Pott 11213 +; C–F +LHP Nogueira 291 +. + + + + +FIGURE 2. +Venation patterns of subterminal leaflets. A. + +Mimosa orbignyana + +. B. + +M. amolariensis + +. C. + +M. aguapeia + +. + + + + +FIGURE 3. +Plant on rock-soil environment in Serra do Amolar (Mato Grosso do Sul). A. Virgate habit of + +Mimosa amolariensis + +, plant on rocky outcrop and among savanna grassland. B. White inflorescences. C. Immature fruits. + + + +Taxonomic notes +—We considered that + +M. amolariensis + +as belonging to the ser. + +Piresianae + +sensu + +Borges +et al +. (2022) + +, since the presence of efoliate panicles and racemes, filiform setae in the pedicel, calyx paleaceous-pappiform, corolla funnelform-like (trumpet-shaped). In addition, the phylogenetic position of this species coincides with the placement in the ser. + +Piresianae + +. It was detected by the inclusion of a distinctly identified sample in recent phylogenetic analyses ( + +Borges +et al +. 2022 + +). The representatives of this series have leaflets more than +10 mm +wide ( + +M +. +kulhmannii + +, + +M +. +macropogon + +, + +M +. +piresii + +and + +M +. +suberosa + +) or leaflets less than +10 mm +wide ( + +M +. +aguapeia + +, + +M +. +amolariensis + +, + +M +. +dasilvae + +, + +M +. +huanchacae + +, + +M. orbignyana + +and + +M. riedelii + +). Among the species with leaflets up to +10 mm +wide, + +M +. +amolariensis + +stands out by glandular trichomes in petiole and craspedia (in contrast to petiole and craspedia without glandular trichomes in + +M. dasilvae + +, + +M. huanchacae + +and + +M. riedelii + +), the largest penultimate leaflet more than +12 mm +length and the excentric veins divide the blade in 1:1:2 (opposite to + +M +. +orbignyana + +in which the largest penultimate leaflet up to +12 mm +length and the central vein divide the blade in 1:2), the secondary veins not anastomosed and the lobes of calyx truncated (unlike the secondary veins anastomosed and the lobes of calyx triangular in + +M +. +aguapeia + +). + + + + +Distribution and habitat +—To date, + +Mimosa amolariensis + +has four known populations in the Serra do Amolar ( +Mato Grosso do Sul +) and Serra de Santa Bárbara ( +Mato Grosso +), in rocky outcrops of Campo Rupestre and Cerrado Rupestre at altitudes of +496–920 m +asl. In hills of Serra do Amolar, + +M. amolariensis + +occurs in higher altitude areas, where the vegetation consists of grasses (different +Poaceae +species), + +Vellozia variabilis +Mart. ex Schult. & Schult.f. + +, and + +Mimosa xanthocentra +Mart. var. +xanthocentra + +also occur, as well as scattered woody species such as + +Diptychandra aurantiaca +Tul. + +, + +Kielmeyera rubriflora +Cambess. + +, + +Miconia ferruginata +DC. + +, + +Styrax ferrugineus +Nees & Mart. + +, and + +Zeyheria montana +Mart. In + +the restricted population at Morro Alegre hill (Serra do Amolar), we found six individuals in dried stream, between rocky outcrops, behind the top of the hill ( +Fig. 3 +). + + + + +Phenology +—Flowering and fruiting occur between March and July and individuals having only fruits were recorded until September. Some morphological traits, such as dehiscent articles, suggest that autochory is the main syndrome related to fruit dispersal. We did not detect morphological traits related to other syndromes. + + + +Ecology— +Mimosa amolariensis + +is characterized by robust underground structures above the rocky outcrops, phenolic compounds stored in its morphological anatomy, and high fruit production ( +Figs. 4 +and +5 +). These traits are associated with the ability to permanency and regrow after periodic natural or anthropological fire events in Serra do Amolar and Serra de Santa Bárbara, including the presence of phenolic compounds, highly associated with protecting the species and increasing its tolerance to fire ( + +Simon +et al +. 2009 + +; + +Palermo +& Miranda +2012 + +; + +Lamont +et al +. 2018 + +; + +Santacruz-Garcia +et al +. 2021a + +; + +Santacruz-Garcia +et al +. 2021b + +; Silva +et al +. 2021; Siqueira +et al +. 2023). The presence of phenolic compounds was detected in other fire-tolerant plants from the Brazilian Pantanal, such as + +Cassia grandis + +L.f., + +Handroanthus heptaphyllus +(Vell.) Mattos + +, + +Inga vera +Willd. + +, + +Ocotea diospyrifolia +(Meisn.) Mez + +, + +Rhamnidium elaeocarpum +Reissek + +, + +Triplaris americana + +L., + +T +. +gardneriana +Wedd. + +and + +Vitex cymosa +Bertero ex Spreng. + +(Silva +et al. +2021; Siqueira +et al +. 2023). + + + + +Etymology +—The specific epithet + +amolariensis + +refers to the location of the first recording of the species, the Serra do Amolar. + + + + +Specimens examined +— + +Brazil +. +Mato Grosso do Sul +: +Corumbá +: +Reserva Acurizal +, +Serra do Amolar +, borda oeste do +Pantanal +, fl. and fr., +17°54’27.0”S +, +57°34’8.0”W +, + +710 m + +, + +10 May 2003 + +, + +A Pott +11213 + +(CGMS) + +; + +Serra do Amolar +, +Pico do Morro do Mandioré +, only fruits, +18°02’37.0”S +, +57°32’47”W +, + +920 m + +, + +14 Sep 2008 + +, + +GA Damasceno-Júnior +5105 + +(CGMS) + +; + +Serra do Amolar +, +Fazenda Morro Alegre +, fl. and fr., +18°01’24.28”S +, +57°31’46.90”W +, + +496 m + +, + +26 Jul 2023 + +, +LHP Nogueira 291 +(CGMS). + + +Mato Grosso +: Pontes e Lacerda, +Serra de Santa Bárbara +, +45 km +em vicinal a partir do km 28 da MT-473, ao sul +de Pontes +e Lacerda, only flowers, +15°41’10.00”S +, +59°21’41.99”W +, + +540 m + +, + +24 Mar 2014 + +, + +MF Simon +2326 + +(CEN) + +. + + + + \ No newline at end of file diff --git a/data/03/DA/87/03DA87BEFFA7FFD407F2EC60769A426A.xml b/data/03/DA/87/03DA87BEFFA7FFD407F2EC60769A426A.xml new file mode 100644 index 00000000000..17fc7369b04 --- /dev/null +++ b/data/03/DA/87/03DA87BEFFA7FFD407F2EC60769A426A.xml @@ -0,0 +1,626 @@ + + + +A new species of Mimosa (Leguminosae, ser. Piresianae) from the Brazilian Midwest + + + +Author + +Nogueira, Luan H. P. +0009-0002-3108-262X +Programa de Pós-graduação em Biologia Vegetal, Instituto de Biociências, Universidade Federal de Mato Grosso do Sul, Avenida Senador Felinto Muller, s. n., Cidade Universitária, Campo Grande, Mato Grosso do Sul, 79070 - 900, Brazil +luanhpnogueira@gmail.com + + + +Author + +Morales, Matías +0000-0001-5540-9725 +Instituto de Recursos Biológicos (IRB), Instituto Nacional de Tecnología Agropecuaria (INTA), Los Reseros y N. Repetto, s / n, Hurlingham, Buenos Aires, Argentina & Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Godoy Cruz 2290, CABA, Argentina +mmorales0007@gmail.com + + + +Author + +Sartori, Ângela L. B. +0000-0002-5911-8797 +Laboratório de Sistemática Vegetal, Instituto de Biociências, Universidade Federal de Mato Grosso do Sul, Avenida Senador Felinto Muller, s. n., Cidade Universitária, Campo Grande, Mato Grosso do Sul, 79070 - 90, Brazil +albsartori@gmail.com + +text + + +Phytotaxa + + +2024 + +2024-08-06 + + +662 + + +1 + + +80 +92 + + + + +https://doi.org/10.11646/phytotaxa.662.1.6 + +journal article +307355 +10.11646/phytotaxa.662.1.6 +912b9bbd-fda4-482a-9373-8197a26613e4 +1179-3163 +14516570 + + + + + +Synopsis for the ser. +Piresianae +(sensu +Borges et al. 2022 +) + + + + + +Series + +Piresianae +Barneby. + + + + + +Type +— + +Mimosa piresii +Barneby + + + + + +Subshrubs or shrubs, prostrate or virgate. Stems unarmed. Microphyllidious or macrophyllidious, usually with few ample leaves, long efoliate terminal panicles or racemes. Indumentum smooth or scaberulous, with glandular setiform trichomes in little species and resinous stems in + +M +. +macropogon + +. Stipules firm or subfoliaceous, either lanceolate or narrowly triangular, the venation immersed. Leaves 1–28 jugate, and pinnae 5–42 pairs of leaflets. Blades 0.4–70 x +2.5–40 mm +, 3–5-nerved. Globose capitula prior to anthesis either moriform or conelike; flowers 4-merous; calyx paleaceous-pappiform; corolla +2.6–5.45 mm +, lobes 1-nerved; androecium diplostemonous, either cream-white or pink, shortly monadelphous. Pods subsessile or shortly stipitate, the shape linear, 25–66.15 × +5–9.55 mm +, 4–12-seeded, the replum +0.4–2 mm +wide; the articles either indehiscent or tardily dehiscent. + + + + +Distribution +—This series has ten species occurring in Neotropical Savannas, southern Brazilian Amazonia, Rupestrian Grassland and Tropical Forest, in +Bolivia +and +Brazil +, distributed at high or low elevations. + + + + +Species— + +M. aguapeia +Barneby + +, + +M. amolariensis +L.H.P.Nogueira, A.L.B.Sartori & M.Morales + +, + +M. dasilvae +A.S.L.Silva & Secco + +, + +M. huanchacae +Barneby + +, + +M. kuhlmannii +Hoehne + +, + +M. macropogon +Barneby + +, + +M. piresii +Barneby + +, + +M. orbignyana +Barneby + +, + +M. riedelii +Benth. + +and + +M. suberosa +Atahuachi & C.E.Hughes. + + + +Described by +Barneby (1991) +, the + +Piresianae + +series originally included only the species + +M +. +kuhlmannii + +, + +M +. +macropogon + +, and + +M +. +piresii + +. Subsequently, + +M +. +dasilvae +( +Silva & Secco 2000 +) + +and + +M +. +suberosa +( +Atahuachi & Hughes 2006 +) + +were added to the ser. + +Piresianae + +because of their affinities to + +M +. +piresii + +. + +Borges +et al +. (2022) + +, through phylogenetic studies in clade O, which was detected in the studies of + +Simon +et al +. (2011) + +, which included ser. + +Pachycarpae + +and ser. +Setosae +, recognizing the monophyly of ser. + +Piresianae + +with the inclusion of + +M +. +aguapeia + +, + +M +. +orbignyana + +, and + +M +. +riedelii + +, these three previously placed by Barneby in ser. +Setosae +. Although + +M. huanchacae + +was not analyzed by + +Borges +et al. +(2022) + +in their study, we considered in it ser. + +Piresianae + +because of the affinity with + +M. aguapeia + +and the previous placement in ser. +Setosae +by +Barneby (1993) +. Additionally, a sample of the specimen +Simon 2326, +which were previously identified as + +M. aguapeia + +and considered here as + +M. amolariensis +, + +was located in the clade + +Piresianae + +( + +Borges +et al. +2022 + +). It reinforces our hypothesis regarding + +M. amolariensis + +belongs to the series + +Piresianae + +. + + + + +FIGURE 6. +Geographic distribution of ser. + +Piresianae + +species in South America. + + + + + +Key for the identification of ser. +Piresianae +species + + + + + + +1. Leaves with pinnae 1-jugate; replum +1.5–2 mm +wide ................................................................................................. + +M +. +kuhlmannii + + + + + +- Leaves with pinnae 2–28-jugate; replum +0.4–1 mm +wide .................................................................................................................2 + + + + + + +2. Resinous stem; foliaceous stipules +1.5–3.5 cm +long .................................................................................................. + +M +. +macropogon + + + + + +- Non-resinous stem; subcoriaceous stipules +0.4–1.2 cm +long.............................................................................................................3 + + + + + + +3. Margin of leaflet glabrous; venation acrodromous........................................................................................................... + +M +. +suberosa + + + + +- Margin of leaflet strigose or pubescent; venation actinodromous......................................................................................................4 + + + + + +4. Procumbent shrubs; stipules 9 × +0.6 mm +, linear-triangular; peduncles strigose ............................................................... + +M +. +dasilvae + + + + + +- Subshrubs to shrubs virgate; stipules 3–12.25 × +1.4–4 mm +, lanceolate, triangular, or ovate; peduncles densely silky ....................5 + + + + + + +5. Leaf petiole +2.5–3 mm +long; pinnae 18–28-jugate.............................................................................................................. + +M. riedelii + + + + + +- Leaf petiole +16–60 mm +long; pinnae 3–14-jugate..............................................................................................................................6 + + + + + + +6. Leaflets 5–9-jugate; blades +10–25 mm +wide........................................................................................................................ + +M. piresii + + + + + +- Leaflets 17–35-jugate; blades +2.6–8.2 mm +wide................................................................................................................................7 + + + + + + +7. Trichomes hispid in stem, glandular trichomes absent in the petiole and fruits; calyx +1.4 mm +long ......................... + +M. huanchacae + + + + + +- Trichomes adpressed in stem, glandular trichomes often in the petiole and fruits; calyx (1.7–) +2.3–3.5 mm +long............................8 + + + + + + +8. Secondary veins of penultimate leaflets reaching the margin, areolation moderately developed and triangular; calyx lobes triangular.......................................................................................................................................................................... + +M. aguapeia + + + + +- Secondary veins of penultimate leaflets not reaching the margin, areolation moderately developed and quadrangular; calyx lobes truncate ...............................................................................................................................................................................................8 + + + + + +9. Largest penultimate leaflet up to +11.8 mm +length; the center vein divides the blade 1:2; trichomes dense-setiform and yellowish in herbarium...................................................................................................................................................................... + +M. orbignyana + + + + + +- Largest penultimate leaflet up to +21.5 mm +length; the subcenter vein divides the blade 1:1:2; trichomes scattered-setiform and white-stramineous in herbarium................................................................................................................................. + +M. amolariensis + + + + + + + + + +Distribution of ser. +Piresianae + + + + + +The +ser. + +Piresianae + +species, restrict only to +South America +, occur in low elevation forests and hill formations at +Brazil +and +Bolivia +. ( +Fig. 5 +). + +M. piresii +Barneby + +is widely distributed in the +Brazilian +states of +Mato Grosso +, +Pará +, +Tocantins +and +Beni +, across locations below + +250 m + +als; in the mountains, the species occurs at higher altitudes, with records of occurrence between +750–820 m +such as Canaã dos Carajás (Pará). + +M. macropogon +Barneby + +predominates in the southern forests of Amazonas, in lower altitude environments ( +50–185 m +als). + +M. kuhlmannii +Hoehne + +and + +M. dasilvae +A.S.L. Silva & Secco + +, respectively, have been recorded in Rondônia and Pará, but there is no precise information about their site of occurrence. + + +In +Bolivia +, + +M. orbignyana + +occurs on hills above +700 m +als, + +M. suberosa +Atahuachi & C.E.Hughes + +and + +M. huanchacae +Barneby + +are found in humid grasslands, Cerrado, and rocky outcrops of Campo Rupestre at altitudes of +200–850 m +als. + +M. aguapeia + +, + +M. orbignyana + +and + +M. suberosa + +can be found in the Brazilian state of Mato Grosso, around the hills of Serra Ricardo Franco State Park. + +M. riedellii + +was only recorded from the Chapada dos Guimarães, Mato Grosso. + +Mimosa amolariensis + +occurs in the Serra do Amolar (Mato Grosso do Sul) and in the Serra de Santa Bárbara (Mato Grosso). + + + + \ No newline at end of file diff --git a/data/17/37/8D/17378D71DA3D5C7A8255B768107F116B.xml b/data/17/37/8D/17378D71DA3D5C7A8255B768107F116B.xml new file mode 100644 index 00000000000..04991c99b2a --- /dev/null +++ b/data/17/37/8D/17378D71DA3D5C7A8255B768107F116B.xml @@ -0,0 +1,116 @@ + + + +Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species + + + +Author + +Ham, Daseul +0000-0002-1900-3637 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea & Species Diversity Research Division, Biodiversity Research Department, National Institute of Biological Resources, Incheon, Republic of Korea + + + +Author + +Bae, Yeon Jae +0000-0001-7810-5409 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea + +text + + +ZooKeys + + +2025 + +2025-01-09 + + +1223 + + +221 +245 + + + +journal article +10.3897/zookeys.1223.128062 +731a7009-110a-4454-838b-7a8f9e4954bb + + + + + +Campylomyza cornuta +Jaschhof, 1998 + + + + + + + + +Campylomyza cornuta + +Jaschhof 1998 b +: 260–261, Abb. 1 a – e. + + + + + + + + +Specimens examined. + + + +Korea +• +2 ♂♂ +(slides no. +NIBRIN 0000941945 +, +NIBRIN 0000992653 +); + +HN + +; + +3 Mar. – 12 Apr. 2019 + +; +H. S. Ahn +leg.; deposited in + +NIBR + + +. + + + + +Distribution. + + +Sweden +, +Lithuania +, +Germany +, and new to +South Korea +. + + + + \ No newline at end of file diff --git a/data/36/68/EB/3668EB2BE84E53D989C67C09FC656247.xml b/data/36/68/EB/3668EB2BE84E53D989C67C09FC656247.xml new file mode 100644 index 00000000000..56ee5141b4d --- /dev/null +++ b/data/36/68/EB/3668EB2BE84E53D989C67C09FC656247.xml @@ -0,0 +1,298 @@ + + + +Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species + + + +Author + +Ham, Daseul +0000-0002-1900-3637 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea & Species Diversity Research Division, Biodiversity Research Department, National Institute of Biological Resources, Incheon, Republic of Korea + + + +Author + +Bae, Yeon Jae +0000-0001-7810-5409 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea + +text + + +ZooKeys + + +2025 + +2025-01-09 + + +1223 + + +221 +245 + + + +journal article +10.3897/zookeys.1223.128062 +731a7009-110a-4454-838b-7a8f9e4954bb + + + + + +Campylomyza hori + +sp. nov. + + + + +Fig. 4 D – F + + + + +Type material examined. + + + + +Holotype + +: +Korea +• +1 ♂ +(slide no. 19 I- 5); +Gangwon-do +, +Jeongseon-gun +, +Jeongseon-eup +, +Hoedong-ri +, 870, +Gariwangsan Recreational Forest + +( +Gariwang +) + +; + +13 Apr. – 12 May 2019 + +; +D. Ham +, +S. Park +leg.; deposited in + +KU + + +. + + +Paratype + +: +Korea +• +1 ♂ +(slide no. +NIBRIN 0000919401 +); same data as holotype and deposited in + +NIBR + + +. + + + + +Other material examined. + + + +Korea +• +2 ♂♂ +(slides no. +NIBRIN 0000992654 +, +NIBRIN 0000992655 +); + + +Sobaek + + +; + +6 May – 6 Jun. 2019 + +; +D. Ham +, +S. Park +leg.; deposited in + +NIBR + + +. + + + + +Diagnosis. + + + +Campylomyza hori + +sp. nov. +is most similar to + +C. mohrigi +Jaschhof, 2009 + +, especially in having the apical points divided, and the dorsal processes with sclerotized ridge, subtriangular apex on tegmen. However, + +C. hori + +sp. nov. +can be distinguished from + +C. mohrigi + +by the following characteristics: 1) Necks of antennal flagellomeres longer than nodes; 2) Gonostyli slightly longer and narrower (Fig. +4 E +); 3) Dorsal processes wider, margin sclerotized, with subtriangular apex, center membranous (Fig. +4 F +, ↓ +13 +) vs. narrower, leaf-shaped with sclerotized ridge and points apically in + +C. mohrigi + +. + + + + +Measurements. + + +Male adult ( +holotype +). Body length +1.441 mm +, wing length +1.645 mm +. Hind leg coxa +0.156 mm +; femur +0.607 mm +; tibia +0.647 mm +; tarsomere I +0.351 mm +; tarsomere II +0.180 mm +; tarsomere III +0.141 mm +; tarsomere IV +0.088 mm +; tarsomere +V +0.070 mm +. + + + + +Description. + + +Male adult ( +holotype +). + +Head +. + +Postocular bristles three. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomere longer than node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. +Thorax. +Preepisternum with five fine setae anteriorly. Wing length to width ratio 2.47. AntC ending beyond +R +4 + 5 +but before reaching; ApicR +1 +2.77 × length of Rs. CuA separated. Tarsomere I longer than tarsomere II. Claws sickle-shaped, weakly toothed; empodia as long as claws; pubescent. + +Terminalia +. + +Tg 9 tapering towards apex with six fine setae apically. Ventral emargination deep, U-shaped, ventral bridge short. Dorsal transverse bridge broadly rounded apically, slightly extended beyond ventrobasal margin (Fig. +4 D +, ↓ +10 +). Gonostyli elongated apically, curved anteroventrally, constricted ventrosubapically (Fig. +4 D +, ↓ +11 +) with fine setae denser towards apex; incised dorsomesally. On tegmen, apical points pointed, directed posteriorly (Fig. +4 F +, ↓ +12 +); dorsal processes broad basally, constricted medially, pointed apically (Fig. +4 F +, ↓ +13 +), directed anterodorsally, with strongly sclerotized margin basally; mesal points faint, short, pointed (Fig. +4 F +, ↓ +14 +). Tegmen shoulders almost angular, equipped with several small bumps laterally (Fig. +4 F +, ↓ +15 +). Transverse brace with lobe-like dorsal extensions. Ejaculatory apodeme swelling medially (Fig. +4 D +, ↓ +16 +), narrow basally. + + + + +Etymology. + + +The species epithet + +hori + +originates from the Korean native term, pronounced + +‘ +hori + +- + +hori + +- hada’, an adjective describing a slender or tapered part. This name specifically denotes the narrowed part of the gonostyli. + + + + \ No newline at end of file diff --git a/data/39/1D/88/391D8874F1485D67B6E6E652389517BB.xml b/data/39/1D/88/391D8874F1485D67B6E6E652389517BB.xml new file mode 100644 index 00000000000..5a5d5dc1b31 --- /dev/null +++ b/data/39/1D/88/391D8874F1485D67B6E6E652389517BB.xml @@ -0,0 +1,223 @@ + + + +Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species + + + +Author + +Ham, Daseul +0000-0002-1900-3637 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea & Species Diversity Research Division, Biodiversity Research Department, National Institute of Biological Resources, Incheon, Republic of Korea + + + +Author + +Bae, Yeon Jae +0000-0001-7810-5409 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea + +text + + +ZooKeys + + +2025 + +2025-01-09 + + +1223 + + +221 +245 + + + +journal article +10.3897/zookeys.1223.128062 +731a7009-110a-4454-838b-7a8f9e4954bb + + + + + +Campylomyza abjecta +Mamaev, 1998 + + + + + + + + +Campylomyza abjecta + +Mamaev 1998: 6 +. + + + + + + + + + +Campylomyza abjecta + +Jaschhof and Jaschhof 2017: 5 +, fig. 2 A – C (redescription). + + + + + + + + +Distribution. + + +Russia +( +Primorsky +), +Sweden +, new record for +South Korea +. + + + + +Specimens examined. + + + +Korea +• +3 ♂♂ +(slides no. 19 AY- 3, 7, 19 AYa- 9, 10); + + +NERC + + +; + +10–17 Apr. 2019 + +; +Y. J. Choi +, +H. G. Kim +leg.; deposited in + +KU + + +• + +1 ♂ +(slide no. +NIBRIN 0000857557 +); + +KUF + +; + +2–8 Apr. 2017 + +; +D. Ham +leg.; deposited in + +NIBR + + +• + +1 ♂ +(slide no. +NIBRIN 0000992636 +); +SJ 1 +; + +13 Apr. – 4 May 2019 + +; +W. G. Kim +leg.; deposited in + +NIBR + + +• + +1 ♂ +(slide no. +NIBRIN 0000992634 +); +SJ 2 +; + +8–24 Apr. 2020 + +; +W. G. Kim +leg.; deposited in + +NIBR + + +. + + + + + + +Male morphology of + +Campylomyza aborigena +Mamaev, 1998 + +( +A – C +) and + +Campylomyza ambulata + +sp. nov. +( +D – G +) +A +gonocoxites, ventral view, slide no. NIBRIN 0000992639 +B +gonostylus, dorsal view, slide no. NIBRIN 0000992639 +C +tegmen, dorsal view, slide no. 19–38 +D +gonocoxites, ventral veiw, holotype +E – G +tegmen, dorsal view +E +holotype +F +paratype (slide no. NIBRIN 0000919403) +G +paratype (slide no. 19 AY- 9). Scale bars: 0.05 mm. + + + + + \ No newline at end of file diff --git a/data/3B/05/C4/3B05C4F631AD50F7B51A9B5596DE560E.xml b/data/3B/05/C4/3B05C4F631AD50F7B51A9B5596DE560E.xml new file mode 100644 index 00000000000..2b192c43dbd --- /dev/null +++ b/data/3B/05/C4/3B05C4F631AD50F7B51A9B5596DE560E.xml @@ -0,0 +1,439 @@ + + + +Mountainous millipedes in Vietnam. III. Two new dragon millipedes from limestone mountains in northern Vietnam (Polydesmida, Paradoxosomatidae, Hylomus), with an identification key to Vietnamese Hylomus species + + + +Author + +Nguyen, Anh D. +0000-0001-9273-0040 +Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, 18, Hoangquocviet Rd., Caugiay District, Hanoi, Vietnam & Graduate University of Science and Technology, Vietnam Academy of Science and Technology, 18, Hoangquocviet Rd., Caugiay District, Hanoi, Vietnam + + + +Author + +Vu, Tam T. T. +0000-0003-1145-975X +Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, 18, Hoangquocviet Rd., Caugiay District, Hanoi, Vietnam & Graduate University of Science and Technology, Vietnam Academy of Science and Technology, 18, Hoangquocviet Rd., Caugiay District, Hanoi, Vietnam + + + +Author + +Nguyen, Thu-Anh T. +0000-0002-0564-3051 +Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, 18, Hoangquocviet Rd., Caugiay District, Hanoi, Vietnam & Graduate University of Science and Technology, Vietnam Academy of Science and Technology, 18, Hoangquocviet Rd., Caugiay District, Hanoi, Vietnam + +text + + +ZooKeys + + +2025 + +2025-01-09 + + +1223 + + +247 +262 + + + +journal article +307356 +10.3897/zookeys.1223.139649 +91a71722-b3e4-4546-80c4-585504080769 +586F1538-6192-4A99-A3D5-8B37DAECEE58 + + + + + +Hylomus borealis + +sp. nov. + + + + +Figs 5 +, +6 +, +7 + + + + +Material examined. + + + + + +Holotype + +. + +Vietnam +• +1 male +; +Cao Bang Province +, +Pia Oac - Pia Den National Park +, on the way to +Hang Ong +; + +22.5540 ° N +, +105.8622 ° E + +; + +850 m +a. s. l. + +; + +8 May 2021 + +; +Anh D. Nguyen +leg.; bushes; IEBR-Myr 908 H + +. + + + +Paratypes + +. + +Vietnam +• +2 females +; same data as for holotype; IEBR-Myr 908 P + +• + +2 females +; same data as for holotype; IEBR-Myr 906 + +• + +2 females +; same data as for the holotype, but + +8 Jun. 2020 + +; IEBR-Myr 851 + +• + +1 female +; same data as for sample IEBR-Myr 851; IEBR-Myr 854 + +. + + + + +Diagnosis. + + +The species can be discriminated from the congeners by the presence of spiniform paraterga; metaterga densely covered with microgranulations; midbody metaterga with two rows of setiferous spines: 2 + +2 in +anterior row and 2 + 2 near posterior margin, the anterior row hardly seen, the posterior row more distinct; male femora 6 each with a large tubercle ventrally; sternite 5 with a large, sparsely setose, bifid, trapeziform lamina between male coxae 4; epiproct with several evident setiferous knobs near tip; gonopod solenophore partly folded to sheathe distal part of solenomere; tip of solenophore consisting of seven overlapping laminae. + + +The new species is similar to + +H. proximus + +in body size and shape, but the two species are distinguished by the number of metatergal posterior spines (2 + 2 vs 3 + 3), male femoral modifications (femur 6 vs femora 5 & 6), and gonopod conformation. The new species has a well-developed gonopod solenophore (sph); a broadly rounded lamina medialis, partly folded to sheathe distal part of solenomere; and gonopod tip consisting of seven overlapping laminae while + +H. proximus + +has a gonopod femorite that is subequal to the postfemoral region in length; both solenophore and solenomere long; and a serrated solenophore tip. + + + +Hylomus borealis + +sp. nov. +is also similar to + +H. jeekeli +( +Golovatch & Enghoff, 1994 +) + +from northern +Thailand +in terms of general body and gonopod shape. However, the new species can be distinguished from it by the combination of these characters: smaller in size with +10.4 mm +in males and +12.3–13.4 mm +in females (vs +15–16 mm +in males and +18–20 mm +in females); metaterga with 2 + 2 spines in posterior rows (vs 3 + 3 spines); modification in only femur 6 (vs femora 6 and 7); tip of solenophore consisting of seven overlapping laminae and not serrate (vs serrated solenophore). + + + + +Etymology. + + +An adjective epithet + +“ +borealis + +” refers to the northern-most province ( +Cao Bang +) of +Vietnam +, the +type +locality. + + + + +Description. + + +Holotype +length +10.4 mm +, width of mid pro- and metazona +0.6 mm +and +1.8 mm +(distance between two paratergal tips), respectively. Female length +12.3–13.4 mm +, width of mid pro- and metazona 0.9–1.0 mm and +1.7–1.8 mm +, respectively. + + +Coloration +: Generally dark to castaneous brown except paratergal bases, sterna, leg coxae and prefemora whitish-yellow. + + +Head +(Fig. +5 A, B +): Clypeolabral region densely setose, vertex sparsely setose. Epicranial suture distinct, dividing frons into two equal parts; with setae along suture. Antenna slender, extremely long, reaching to body ring 5 if stretched along the body axis; antennomere 1 <7 <6 <2 <3 = 4 = +5 in +length. + + + + + + + +Hylomus borealis + +sp. nov. +, holotype (IEBR-Myr 908 H) +A +anterior-most body part, lateral view +B +frons and collum, anterior view (under UV light) +C +body rings 8–12, dorsal view +D +body rings 8–10, lateral view. Scale bars: 1 mm. + + + +Collum +(Fig. +5 B +): Subequal to head in width; surface dull, coarsely and densely microgranulate, with three rows of spines: 3 + 3 spines in anterior row, 1 + 1 spines in intermediate row, and 2 + 2 spines in posterior row; all spines equal in size. Paratergum well developed; directed dorsad; highly elevated above dorsal surface; with two conspicuous teeth on anterior side. + + +Body rings +: Rings 3 <4 <2 = +5–16 in +width, thereafter gradually tapering towards telson. Prozona finely shagreened; metazona and pleura with microgranulations. Transverse sulcus present, but inconspicuous on metaterga 5–18. Axial line missing. Metaterga with two rows of setiferous spines: 2 + 2 spines in anterior row and 2 + 2 spines near posterior margin (Figs +5 C +, +6 B +), the anterior row hardly visible, the posterior row more distinct (Fig. +6 B +). Suture between pro- and metazona broad, very shallow. Pleurosternal carinae present as a complete keel on body rings 2–3, then missing on subsequent body rings. + + + + + + + +Hylomus borealis + +sp. nov. +, holotype (IEBR-Myr 908 H) +A +body rings 8–10, ventral view +B +body rings 8–10, dorsal view (under UV light) +C +telson, dorsal view (under UV light) +D +sternum 5, subposterior view. Scale bars: 1 mm. + + + +Paraterga +(Fig. +5 +): Very well developed; directed laterodorsad; antler-shaped with a large branch and 2 small teeth on anterior side and 1 smaller spine on posterior side. Ozopore located between the first tooth and main branch of paraterga, visible in dorsal view. + + +Telson +(Fig. +6 C +): Epiproct with several evident setiferous knobs near tip; tip with four spinnerets; lateral tubercles well developed. Hypoproct sub-trapeziform, with two distolateral, completely separated, setiferous knobs. + + +Legs +: Extremely long, slender and thin, c. 1.5–1.6 times as long as midbody height. Prefemora not swollen. Male femora 6 each ventrally with a large, robust tubercle in middle. + + +Sterna +: with distinct cross-impression, no modification – except a large, sparsely setose, trapeziform lamina carrying two distal, separated lobes between male coxae 4 (Fig. +6 D +). + + +Gonopod +(Fig. +7 +): Suberect. Coxite ( +co +) cylindrical, much shorter than femorite, sparsely setose distodorsally. Prefemorite ( +pref +) densely setose, shorter than femorite as well. Femorite ( +fe +) slightly enlarged distad, without a demarcation with postfemoral region. Postfemoral region slightly twisted mesad. Solenophore ( +sph +) well developed; lamina medialis ( +lm +) broadly rounded, partly folded to sheathe distal part of solenomere, lamina lateralis ( +ll +) well developed. Seminal groove running entirely on mesal side, then entering a flagelliform solenomere ( +sl +) which is partly sheathed by solenophore. Tip of gonopod consisting of seven overlapping laminae (Fig. +7 G +). + + + + + + + +Hylomus borealis + +sp. nov. +, holotype (IEBR-Myr 908 H), +SEM +A – D +left gonopod, lateral view ( +A +), ventral view ( +B +), dorsal view ( +C +), mesal view ( +D +) +E – G +distal part of left gonopod, ventral view ( +E +), dorsal view ( +F +) +G +tip of left gonopod, ventral view. Abbreviations: +co += coxite; +pref += prefemorite; +fe += femorite; +ca += canula; +lm += lamina medialis; +ll += lamina lateralis; +sl += solenomere. Scale bars: 200 µm ( +A – D +); 100 µm ( +E +), 50 µm ( +F +), 30 µm ( +G +). + + + + + +DNA barcoding. + + +(Appendix +1 +) A fragment of the +COI +gene is accessioned at +NCBI +GenBank with the following accession number +PQ 676352 +. The new species exhibits a +COI +gene similarity of 85.29 % identity with + +Hylomus proximus +Nguyen, Golovatch & Anichkin, 2005 + +( + + +MG +669371 + + +) and 83.11 % identity with + +Desmoxytes takensis +Srisonchai, Enghoff, Likhitrakarn & Panha, 2016 + +( + +OR +765894 + +). + + + + \ No newline at end of file diff --git a/data/45/1E/00/451E00DA591F584F85A241FC1F6834CC.xml b/data/45/1E/00/451E00DA591F584F85A241FC1F6834CC.xml new file mode 100644 index 00000000000..2da0147514f --- /dev/null +++ b/data/45/1E/00/451E00DA591F584F85A241FC1F6834CC.xml @@ -0,0 +1,347 @@ + + + +Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species + + + +Author + +Ham, Daseul +0000-0002-1900-3637 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea & Species Diversity Research Division, Biodiversity Research Department, National Institute of Biological Resources, Incheon, Republic of Korea + + + +Author + +Bae, Yeon Jae +0000-0001-7810-5409 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea + +text + + +ZooKeys + + +2025 + +2025-01-09 + + +1223 + + +221 +245 + + + +journal article +10.3897/zookeys.1223.128062 +731a7009-110a-4454-838b-7a8f9e4954bb + + + + + +Campylomyza cornigera + +sp. nov. + + + + +Fig. 4 A – C + + + + +Type material examined. + + + + +Holotype + +: +Korea +• +1 ♂ +(slide no. 19 Aya- 8); +Gyeongsangbuk-do +, +Yeongyang-gun +, +Yeongyang-eup +, +Gowol-gil +, 23, +National Endangered Species Restoration Center + +( + +NERC + +) + +; + +10–17 Apr. 2019 + +; +Y. J. Choi +, +H. G. Kim +leg.; deposited in + +KU + + +. + + +Paratype + +: +Korea +• +1 ♂ +(slide no. +NIBRIN 0000857558 +); + +KUF + +; + +2–8 Apr. 2017 + +; +D. Ham +leg.; deposited in + +NIBR + + +. + + + + +Other material examined. + + + +Korea +• +1 ♂ +(slide no. +NIBRIN 0000992637 +); + +Odae +1 + +; + +18 Apr. – 1 May 2020 + +; +D. Ham +, +S. Park +leg.; deposited in + +NIBR + + +. + + + + +Diagnosis. + + + +Campylomyza cornigera + +sp. nov. +is most similar to + +C. nigroliminata +Mamaev, 1998 + +(cf. +Jaschhof and Jaschhof 2021 +: fig. 30 A, B), especially in having lamellate apical points of the tegmen that are rounded apically and pointed processes directed anterolaterad (Fis. 4 C, ↓ +5, 6 +), and mesal processes are directed anteriorly (Fig. +4 C +, ↓ +7 +). However, + +C. cornigera + +sp. nov. +can be distinguished from + +C. nigroliminata + +by the following characteristics: 1) Pointed processes directed anterolaterally of apical points slightly curved; 2) Dorsal processes missing; 3) Tegmen shoulders indistinct. + + + + + + +Male morphology of + +Campylomyza cornigera + +sp. nov. +, holotype +A – C +and + +Campylomyza hori + +sp. nov. +, holotype +D – F +: +A +gonocoxites, ventral view +B +gonostylus, dorsal view +C +tegmen, dorsal view +D +gonocoxites, ventral view +E +gonostylus, dorsal view +F +tegmen, dorsal view. Scale bars: 0.05 mm. + + + + + +Measurements. + + +Male adult ( +holotype +): Body length +1.315 mm +. Wing length +1.574 mm +. Hind leg coxa +0.141 mm +; femur +0.539 mm +; tibia +0.515 mm +; tarsomere I +0.302 mm +; tarsomere II +0.142 mm +; tarsomere III +0.105 mm +; tarsomere IV +0.062 mm +; tarsomere +V +0.056 mm +. + + + + +Description. + + +Male adult ( +holotype +). + +Head +. + +Postocular bristles seven. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomeres as long as node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. + +Thorax +. + +Preepisternum with 1–9 setae. Wing length to width ratio 2.58. AntC ending beyond +R +4 + 5 +but before reaching M +4 +; ApicR +1 +3.08 × length of Rs. CuA separated. Tarsomere I longer than tarsomere II. Claws sickle-shaped, toothed; empodia longer than claws, slightly broaden apically; pubescent. + +Terminalia +. + +Tg 9 tapered towards apex with seven or eight fine setae apically. Ventral bridge of gonocoxites long (Fig. +4 A +, ↓ +1 +), with U-shaped emargination; dorsal transverse bridge narrowly tapering, extending far beyond basal margin (Fig. +4 A +, ↓ +2 +). Ventromedial portion of gonocoxites almost angular (Fig. +4 A +, ↓ +3 +). Gonostyli narrowly rounded to pointed apically (Fig. +4 A +, ↓ +4 +), moderately convex posteriorly, and slightly excavated medially, plump dorsally; setae denser towards apex. Tegmen long and narrow, apical points sclerotized, short, stout, and broadly rounded apically (Fig. +4 C +, ↓ +5 +); a pair of strongly sclerotized processes directed dorsolaterally (Fig. +4 C +, ↓ +6 +); true dorsal processes missing. Mesal points of tegmen slightly sclerotized, narrowly long, directed anteriorly (Fig. +4 C +, ↓ +7 +). Shoulders of tegmen inconspicuous; width between apices of shoulders narrower than processes directed dorsolaterally. Transverse brace rib-shaped (Fig. +4 C +, ↓ +8 +). Parameral apodemes long (Fig. +4 C +, ↓ +9 +). Ejaculatory apodeme of typical + +Campylomyza + +outline. + + + + +Etymology. + + +The species epithet + +cornigera + +, derived from Latin meaning ‘ having horns, ’ refers to the horn-shaped processes on the tegmen that are directed dorsolaterally. + + + + \ No newline at end of file diff --git a/data/47/1D/C7/471DC710F3595A73875832F3C4581E23.xml b/data/47/1D/C7/471DC710F3595A73875832F3C4581E23.xml new file mode 100644 index 00000000000..88b23096c0c --- /dev/null +++ b/data/47/1D/C7/471DC710F3595A73875832F3C4581E23.xml @@ -0,0 +1,753 @@ + + + +Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species + + + +Author + +Ham, Daseul +0000-0002-1900-3637 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea & Species Diversity Research Division, Biodiversity Research Department, National Institute of Biological Resources, Incheon, Republic of Korea + + + +Author + +Bae, Yeon Jae +0000-0001-7810-5409 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea + +text + + +ZooKeys + + +2025 + +2025-01-09 + + +1223 + + +221 +245 + + + +journal article +10.3897/zookeys.1223.128062 +731a7009-110a-4454-838b-7a8f9e4954bb + + + + + +Campylomyza salicia + +sp. nov. + + + + +Fig. 5 E – G + + + + +Type material examined. + + + + +Holotype + +: +Korea +• +1 ♂ +(slide no. 19 Aya- 2); +Gyeongsangbuk-do +, +Yeongyang-gun +, +Yeongyang-eup +, +Gowol-gil +, 23, +National Endangered Species Restoration Center + +( + +NERC + +) + +; + +10–17 Apr. 2019 + +; +Y. J. Choi +, +H. G. Kim +leg.; deposited in + +KU + + +. + + +Paratypes + +: +Korea + +• + +5 ♂♂ +(slides no. 19 AY- 5, 10, 13, 17, 19 AYa- 13); same data and deposition as +holotype + +• + +1 ♂ +(slide no. +NIBRIN 0000919404 +); same data as holotype, deposited in + +NIBR + + +. + + + + +Other material examined. + + + +Korea +• +2 ♂♂ +(slides no. 19 AZ- 6, 9); + + +NERC + + +; + +3–10 Apr. 2019 + +; +Y. J. Choi +, +H. G. Kim +leg.; deposited in + +KU + + +• + +1 ♂ +(slide no. 19 AX- 4); + + +NERC + + +; + +20–27 Mar. 2019 + +; +Y. J. Choi +, +H. G. Kim +leg.; deposited in + +KU + + +• + +1 ♂ +(slide no. +NIBRIN 0000992640 +); + + +NERC + + +; + +27 Mar. – 3 Apr. 2019 + +; +Y. J. Choi +, +H. G. Kim +leg.; deposited in + +NIBR + + +. + + + + +Diagnosis. + + + +Campylomyza salicia + +sp. nov. +is most similar to + +C. mohrigi + +(cf. illustration of +Jaschhof and Jaschhof 2009: 109 +), especially having the elongated, tapering Gonostyli ventrally, not lamellate apical points and foliate dorsal processes which reaching to transverse brace on tegmen. However, + +C. salicia + +sp. nov. +can be distinguished from + +C. mohrigi + +by following characteristics: 1) dorsal processes of tegmen sclerotized margin without sclerotized ridge (Fig. +5 G +, ↓ +9 +); 2) the dorsal processes are directed dorsolaterally with a strongly sclerotized triangular apex; 3) parameral apodeme shorter than that of + +C. mohrigi + +(Fig. +5 G +, ↓ +10 +). + + + + +Measurements. + + +Male adult ( +holotype +): Body length +0.944 mm +. Wing length +1.266 mm +. Hind leg coxa +0.142 mm +; femur +0.441 mm +; tibia +0.463 mm +; tarsomere I +0.275 mm +; tarsomere II +0.123 mm +; tarsomere III +0.103 mm +; tarsomere IV +0.072 mm +; tarsomere +V +0.057 mm +. + + + + +Description. + + +Male adult ( +holotype +). Slightly smaller than other + +Campylomyza +species. + + +Head +. + +Postocular bristles five. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomere longer than node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. + +Thorax +. + +Preepisternum with six fine setae anteriorly. Wing length to width ratio 2.70. AntC ending beyond +R +4 + 5 +but before reaching M +4 +; ApicR +1 +3.23 × length of Rs; CuA separated. Tarsomere I longer than tarsomere II. Claws slightly toothed; empodia small, narrow. + +Terminalia +. + +Tg 9 tapered towards apex with 8 setae apically. Ventral bridge of gonocoxites half-length of gonocoxites; dorsal transverse bridge tapering, extending beyond ventrobasal margin. Ventral emargination U-shaped. Gonostyli elongated, blunt to slightly pointed apically, moderately convex apically; ventrosubapically constricted (Fig. +5 E +, ↓ +7 +); excavated ventromesally; setae denser towards apex. On tegmen, apical points triangular shaped, not lamellate, pointed apically, directed posterolaterally (Fig. +5 G +, ↓ +8 +); dorsal processes leaf-shaped, elongated slightly beyond transverse brace, with strongly sclerotized apex (Fig. +5 G +, ↓ +9 +). Shoulders of tegmen well developed, thick. Transverse brace slightly extended, lobe shaped. Parameral apodemes short (Fig. +5 G +, ↓ +10 +). + + + + +Etymology. + + +The species name + +salicia + +is derived from the Latin word +salici +, meaning ‘ willow, ’ in reference to the dorsal processes of the tegmen, which resembles the shape of a willow leaf. + + + +Key to the Species of Korean +<taxonomicName id="F1C7E3CFA6F24F22028A35DB15655A4A" authorityName="Meigen" authorityYear="1818" class="Insecta" family="Cecidomyiidae" genus="Campylomyza" kingdom="Animalia" order="Diptera" phylum="Arthropoda" rank="genus"> +<emphasis id="1805B201C89F69258D018A0D3BF3F7FB" italics="true">Campylomyza</emphasis> +</taxonomicName> + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
1Ejaculatory apodeme without apical extension. Tegmen without dorsal processes + + +C. cornuta +Jaschhof, 1998 + + +
–Ejaculatory apodeme with apical extension. Tegmen bearing apical points and processes +2 +
2On tegmen, dorsal processes forming mesal cleft with expended subtriangular processes laterally + + +C. odae + +sp. nov. +(Fig. +5 A – D +) + +
–On tegmen, dorsal processes elongated without mesal cleft or absent, or dorsomesal processes present +3 +
3On tegmen, apical points present; dorsal processes elongated, foliate or dorsolaterad processes horn-shaped at apex; shoulders well developed + + +flavipes + +group, 4 + +
–On tegmen, dorsal processes absent or single pair of small dorsomesal processes present +12 +
4Gonostyli short, ovoid-shaped; not pointed + + +C. abjecta +Mamaev, 1998 + + +
–Gonostyli elongated, curved inwardly +5 +
5Gonostyli elongated, strongly curved inwardly; constricted ventrosubapically with dense setae apically. On tegmen, apical points sharp apically +6 +
–Gonostyli blunt, rounded apically; slightly curved inwardly +7 +
6Ventral bridge of gonocoxites shorter than half-length of gonocoxites. Dorsal processes wide, constricted at middle length with sclerotized subtriangular points on tegmen + + +C. hori + +sp. nov. +(Fig. +4 D – F +) + +
–Ventral bridge of gonocoxites half-length of gonocoxites. Dorsal processes tapering sclerotized along margin, beyond transverse brace. Parameral apodeme short + + +C. salicia + +sp. nov. +(Fig. +5 A – D +) + +
7On tegmen, apical points rounded apically, parallel-sided +8 +
– +On tegmen, apical points pointed at apex (apical points of + +C. ambulata + +typically pointed, subtriangular, but occasionally bulged with round serrated surfaces) + +10 +
8Gonocoxites with swollen, pronounced ventromedial portion. On tegmen, dorsal processes spoon-shaped; elongated with subtriangular narrow tips apically, directed anteriorly + + +C. aborigena +Mamaev, 1998 + +(Fig. +2 A – C +) + +
–On tegmen, dorsal processes horn-shaped, sclerotized apically, directed laterally +9 +
9On tegmen, apical points rounded, short, slightly curved anterolaterally + + +C. cornigera + +sp. nov. +(Fig. +4 A – C +) + +
–Gonostyli with small dorsomedial lobe. On tegmen, apical points long, parallel-sided to rounded apically; dorsal processes strongly sclerotized, straightened, directed dorsolaterally with triangular apex + + +C. convexa + +sp. nov. +(Fig. +3 D – F +) + +
10On tegmen, apical points pointed or broadly rounded apically with serrated surfaces; dorsal processes elongated, directed anteriorly + + +C. ambulata + +sp. nov. +(Fig. +2 D – G +) + +
–On tegmen, dorsal processes with subtriangular apex, directed anterolaterally +11 +
11Gonostyli slightly excavated mesally, flattened dorsally, narrowly rounded apically with convex apical margins; Tegmen apical points lamellate; dorsal processes foliate, directed anterolaterally + + +C. flavipes +Meigen, 1818 + + +
–Gonostyli neither curved nor excavated; tegmen apical points lamellated with dorsal processes elongated and foliate; sclerotized along margins and directed anterolaterally or anteriorly + + +C. furva +Edwards, 1938 + + +
12On tegmen, apical points tapering; dorsal processes absent; mesal processes rounded at apex; shoulders indistinct or missing + +ormerodi +group, 13 + +
–Tegmen with 1 pair of small dorsomesal processes which are serrated or extended +14 +
13Tg 9 tapering broadly. Cerci with strikingly large pubescence. Tegmen shoulders inconspicuous; parameral apodeme long, more than half-length of tegmen + + +C. angusta + +sp. nov. +(Fig. +3 A – C +) + +
–Tg 9 tapering narrowly. Gonocoxites with protruding portion dorsomesally. On tegmen, apical points slightly serrated; shoulder indistinct. Parameral apodeme short + + +C. cavitata +Mamaev, 1998 + + +
14Tegmen processes serrated + +serrata +group, 15 + +
–On tegmen, apical points rounded on apex in ventral view; medial structure strongly sclerotized, connected with triangular structure below + + +C. cingulata +Jaschhof, 2009 + + +
15Gonostyli with lobe dorsally. Serrated processes on tegmen situated subapically dorsomedially in longitudinal direction. Aedeagal head small + + +C. appendiculata +Jaschhof, 2015 + + +
–Medial bridge of gonocoxites with one spine, one pubescent projection. Serrate processes on tegmen turned posteriorly forming apex of tegmen. Aedeagal head large + + +C. spinata +Jashchhof, 1998 + + +
+ + + +DNA barcode analysis and +<collectionCode id="98FB83C3C208BB7A53709723FE51B830">MOTU</collectionCode> +estimation + + + +The 658 - bp +COI +sequences were analyzed, revealing 234 variable sites, of which 63 were parsimony informative. Within the genus + +Campylomyza + +, the interspecific divergences ( +p +- distances) ranged from 6.18 % to 15.28 %. The mean distance across the entire dataset was 10.72 % (Suppl. material +1 +: table S 3). Intraspecific genetic distances varied from 0 % to 0.92 %. The species delimitation using the + +ABGD + +method delineated 17 Molecular Operational Taxonomic Units ( +MOTUs +), including the outgroup. These +MOTUs +are illustrated by the color bars on the Neighbor Joining ( + +NJ + +) tree in Fig. +6 +, corresponding with the delineations observed in the same +NJ +tree. All 17 +MOTUs +correspond to groups distinguished by their morphological characteristics. + + + + + + +Neighbor-joining ( +NJ +) Kimura- 2 - parameter tree derived from the +COI +analysis of sixteen Korean + +Campylomyza +species + +, with + +Peromyia trifida + +as the outgroup. Numbers at the nodes represent +NJ +bootstrap support values. The vertical purple color bar on the right represents results from the +ABGD +delimitation method. + + + + + \ No newline at end of file diff --git a/data/52/FC/3E/52FC3E3F8F3D51739C8D1A6378DC38C6.xml b/data/52/FC/3E/52FC3E3F8F3D51739C8D1A6378DC38C6.xml new file mode 100644 index 00000000000..39a560feb71 --- /dev/null +++ b/data/52/FC/3E/52FC3E3F8F3D51739C8D1A6378DC38C6.xml @@ -0,0 +1,327 @@ + + + +Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species + + + +Author + +Ham, Daseul +0000-0002-1900-3637 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea & Species Diversity Research Division, Biodiversity Research Department, National Institute of Biological Resources, Incheon, Republic of Korea + + + +Author + +Bae, Yeon Jae +0000-0001-7810-5409 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea + +text + + +ZooKeys + + +2025 + +2025-01-09 + + +1223 + + +221 +245 + + + +journal article +10.3897/zookeys.1223.128062 +731a7009-110a-4454-838b-7a8f9e4954bb + + + + + +Campylomyza convexa + +sp. nov. + + + + +Fig. 3 D – F + + + + + +Type +material examined. + + + +Korea +• + +1 ♂ +(slide no. HDS- 505); +Gyeonggi-do +, +Namyangju-si +, +Wabu-eup +, +Dosim-gil +, +Korea +University’s +farm to practice + +( + +KUF + +) + +; + +2–8 Apr. 2017 + +; +D. Ham +leg.; deposited in + +KU + +. + + +Paratypes + + +: +Korea + +• + +1 ♂ +(slide no. HDS- 504); same data and deposition as +holotype + +• + +2 ♂♂ +(slides no. +NIBRIN 0000857555 +, +NIBRIN 0000919405 +) + +KUF + +; + +2–8 Apr. 2017 + +; +D. Ham +leg.; deposited in + +NIBR + + +. + + + + +Other material examined. + + + +Korea +• +4 ♂♂ +(slides no. +NIBRIN 0000992649 +– +NIBRIN 0000992652 +); + +KUF + +; + +2–8 Apr. 2017 + +; +Y. J. Bae +leg.; deposited in + +NIBR + + +. + + + + +Diagnosis. + + + +Campylomyza convexa + +sp. nov. +is most similar to + +C. aemula + +(cf. +Jaschhof and Jaschhof 2009 +: fig. 29 A – D), especially in having the rounded apical points on the tegmen, tapering posteriorly, the dorsal processes are broad basally, directed dorsolaterally with a strongly sclerotized triangular apex. However, + +C. convexa + +sp. nov. +can be distinguished from + +C. aemula + +by following characteristics: 1) Gonostyli moderately convex apically, not excavated medially, broadly rounded apically, with small dorsomedial lobe (Fig. +3 E +, ↓ +8 +); 2) Apical points of tegmen parallel-sided to rounded apically, longer than + +C. aemula +( +Jaschhof and Jaschhof 2009: 102 +) + +; 3) Mesal points of tegmen longer and narrower than in + +C. aemula + +(Fig. +3 E +, ↓ +11 +); 4) Dorsal processes lacking sclerotized ridge, strongly sclerotized apically (Fig. +3 E +, ↓ +10 +). + + + + +Measurements. + + +Male adult ( +holotype +): Body length +1.417 mm +. Wing length +1.639 mm +. Hind leg coxa +0.105 mm +; femur +0.555 mm +; tibia +0.574 mm +; tarsomere I +0.333 mm +; tarsomere II +0.170 mm +; tarsomere III +0.138 mm +; tarsomere IV +0.082 mm +; tarsomere +V +0.065 mm +. + + + + +Description. + + +Male adult ( +holotype +). + +Head +. + +Postocular bristles seven. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomeres shorter than node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. + +Thorax +. + +Preepisternum with nine setae. Wing length to width ratio 2.24. AntC ending beyond +R +4 + 5 +but before reaching M +4 +; ApicR +1 +3.82 × length of Rs. CuA separated. Tarsomere I longer than tarsomere II. Tarsomere I longer than tarsomere II. Claws sickle-shaped, slightly toothed; empodia as long as claws, slightly broaden apically; pubescent. + +Terminalia +. + +Tg 9 tapered towards apex with eight fine setae. Ventral bridge of gonocoxites long, ventral emargination relatively short and broad, U-shaped, dorsal transverse bridge broad, extending far beyond ventrobasal margin. Ventromedial portion of gonocoxites broad, slightly pronounced (Fig. +3 D +, ↓ +7 +). Gonostyli curved anteroventrally, rounded apically, moderately convex apically with small dorsomedial lobe (Fig. +3 E +, ↓ +8 +); setae distributed evenly in ventral view, denser towards apex in dorsal view. On tegmen, apical points long, parallel-sided to rounded apically, not lamellate, sclerotized (Fig. +3 F +, ↓ +9 +); dorsal processes strongly sclerotized apically, directed dorsolaterally (Fig. +3 F +, ↓ +10 +); mesal points weakly sclerotized, faint apically, directed anteriorly (Fig. +3 F +, ↓ +11 +). Shoulders of tegmen inconspicuous. Transverse brace rib-shaped without extension (Fig. +3 F +, ↓ +12 +). Parameral apodeme sclerotized, long, slightly shorter than half of tegmen (Fig. +3 F +, ↓ +13 +). Ejaculatory apodeme of typical + +Campylomyza + +outline. + + + + +Etymology. + + +From the Latin word +convexus +, meaning ‘ a surface with rounded edges’, which refers to the rounded outline of the apex of the apical points on the tegmen. + + + + \ No newline at end of file diff --git a/data/69/FB/E5/69FBE51B451C57A88F21584882A89FC7.xml b/data/69/FB/E5/69FBE51B451C57A88F21584882A89FC7.xml new file mode 100644 index 00000000000..576990223b8 --- /dev/null +++ b/data/69/FB/E5/69FBE51B451C57A88F21584882A89FC7.xml @@ -0,0 +1,393 @@ + + + +Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species + + + +Author + +Ham, Daseul +0000-0002-1900-3637 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea & Species Diversity Research Division, Biodiversity Research Department, National Institute of Biological Resources, Incheon, Republic of Korea + + + +Author + +Bae, Yeon Jae +0000-0001-7810-5409 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea + +text + + +ZooKeys + + +2025 + +2025-01-09 + + +1223 + + +221 +245 + + + +journal article +10.3897/zookeys.1223.128062 +731a7009-110a-4454-838b-7a8f9e4954bb + + + + + +Campylomyza ambulata + +sp. nov. + + + + +Fig. 2 D – G + + + + +Type material examined. + + + + +Holotype + +: +Korea +• +1 ♂ +(slide no. 19 AYa- 11); +Gyeongsangbuk-do +, +Yeongyang-gun +, +Yeongyang-eup +, +Gowol-gil +, 23, +National Endangered Species Restoration Center + +( + +NERC + +) + +; + +10–17 Apr. 2019 + +; +Y. J. Choi +, +H. G. Kim +leg.; deposited in + +KU + + +. + + +Paratypes + +: +Korea + +• + +6 ♂♂ +(slides no. 19 AY- 4, 8, 9, 11, 12, 14, 19 AYa- 6, 12); same data and deposition as +holotype + +• + +1 ♂ +(slide no. 19 AZ- 10); + + +NERC + + +; + +3–10 Apr. 2019 + +; +Y. J. Choi +, +H. G. Kim +leg.; deposited in + +KU + + +• + +1 ♂ +(slide no. +NIBRIN 0000919403 +); + + +NERC + + +; same data as for preceding; deposited in + +NIBR + + +. + + + + +Other material examined. + + + +Korea +• +2 ♂♂ +(slides no. +NIBRIN 0000992627 +, +NIBRIN 0000992628 +); + +Odae +2 + +; + +23 Apr. – 11 May 2019 + +; +D. Ham +, +S. Park +leg.; deposited in + +NIBR + + +• + +1 ♂ +(slide no. HDS- 674); + +GW + +; + +8 Nov. 2017 + +; +D. Ham +leg.; deposited in + +KU + + +• + +1 ♂ +(21 AE- 2-2); + + +GP + + +; + +28 Apr. – 5 May 2019 + +; +Y. J. Bae +leg.; deposited in + +KU + + +• + +1 ♂ +(21 AG- 1-5); +SJ 2 +; + +8–24 Apr. 2020 + +; +W. G. Kim +leg.; deposited in + +KU + + +. + + + + +Diagnosis. + + + +Campylomyza ambulata + +sp. nov. +can be distinguished from other species in the + +flavipes + +group found in +Korea +through the following characteristics: 1) gonostyli curved anteroventrally, excavated ventromesally with denser setae towards the apex; 2) apical point small, short subtriangular (Fig. +2 E +, ↓ +10 +); 3) dorsal processes strongly tapering anteriorly, moveable depending on the pressure (Fig. +2 E +, ↓ +11 +); 4) shoulders of tegmen conspicuous (Fig. +2 E +, ↓ +12 +); 5) parameral apodeme short. + + + + +Measurements. + + +Male adult ( +holotype +): Body length +1.187 mm +. Wing length +1.364 mm +. Hind leg coxa +0.134 mm +; femur +0.480 mm +; tibia 0.500 mm; tarsomere I +0.290 mm +; tarsomere II +0.133 mm +; tarsomere III +0.112 mm +; tarsomere IV +0.071 mm +; tarsomere +V +0.058 mm +. + + + + +Description. + + +Male adult ( +holotype +). + +Head +. + +Postocular bristles 3–5. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomeres as long as node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. + +Thorax +. + +Preepisternum with eight setae. Wing length to width ratio 2.28, AntC ending beyond +R +4 + 5 +but before reaching M +4 +; ApicR +1 +3.46 × length of Rs; CuA separated. Tarsomere I longer than tarsomere II. Claws sickle-shaped, toothed; empodia longer than claws, pubescent. + +Terminalia +. + +Tg 9 tapering towards apex with five fine setae apically. Ventral emargination U-shaped; ventromedial portion of gonocoxites slightly pronounced (Fig. +2 D +, ↓ +8 +). Gonostyli with moderately convex apical margins, excavated ventromedially, narrowly rounded apically. Dorsal transverse bridge broadly rounded apically, extending beyond ventrobasal margin (Fig. +2 D +, ↓ +9 +). On tegmen, apical points small, subtriangular, lamellate (Fig. +2 E +, ↓ +10 +), dorsal processes long, strongly tapering towards apex beyond midlength, blunt apically (Fig. +2 E +, ↓ +11 +). Tegmen shoulders well-developed (Fig. +2 E +, ↓ +12 +), Parameral apodeme short (Fig. +2 E +, ↓ +15 +). + + + + +Variation. + + +We observed significant variation concerning apical points and tegmen shoulders (Fig. +2 F – G +). Apical points bulged with round serrated surfaces (Fig. +2 G +, ↓ +13 +); Shoulders inconspicuous, when almost in the same position or lower than apical points of tegmen (Fig. +2 G +, ↓ +14 +). Dorsal processes moveable apically. + + + + +Etymology. + + +The species epithet + +ambulata + +is derived from the Latin word +ambulātus +, which means ambulatory, referring to the movable nature of the dorsal processes. + + + + \ No newline at end of file diff --git a/data/83/15/24/831524D8E34E5890B8622D92AB730445.xml b/data/83/15/24/831524D8E34E5890B8622D92AB730445.xml new file mode 100644 index 00000000000..a14b3828e89 --- /dev/null +++ b/data/83/15/24/831524D8E34E5890B8622D92AB730445.xml @@ -0,0 +1,426 @@ + + + +Mountainous millipedes in Vietnam. III. Two new dragon millipedes from limestone mountains in northern Vietnam (Polydesmida, Paradoxosomatidae, Hylomus), with an identification key to Vietnamese Hylomus species + + + +Author + +Nguyen, Anh D. +0000-0001-9273-0040 +Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, 18, Hoangquocviet Rd., Caugiay District, Hanoi, Vietnam & Graduate University of Science and Technology, Vietnam Academy of Science and Technology, 18, Hoangquocviet Rd., Caugiay District, Hanoi, Vietnam + + + +Author + +Vu, Tam T. T. +0000-0003-1145-975X +Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, 18, Hoangquocviet Rd., Caugiay District, Hanoi, Vietnam & Graduate University of Science and Technology, Vietnam Academy of Science and Technology, 18, Hoangquocviet Rd., Caugiay District, Hanoi, Vietnam + + + +Author + +Nguyen, Thu-Anh T. +0000-0002-0564-3051 +Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, 18, Hoangquocviet Rd., Caugiay District, Hanoi, Vietnam & Graduate University of Science and Technology, Vietnam Academy of Science and Technology, 18, Hoangquocviet Rd., Caugiay District, Hanoi, Vietnam + +text + + +ZooKeys + + +2025 + +2025-01-09 + + +1223 + + +247 +262 + + + +journal article +307356 +10.3897/zookeys.1223.139649 +91a71722-b3e4-4546-80c4-585504080769 +586F1538-6192-4A99-A3D5-8B37DAECEE58 + + + + + +Hylomus piccolo + +sp. nov. + + + + +Figs 1 +, +2 +, +3 +, +4 + + + + +Material examined. + + + + + +Holotype + +. + +Vietnam +• +1 male +; +Cao Bang Province +, +Pia Oac - Pia Den National Park +; + +22.5943 ° N +, +105.8846 ° E + +; + +1200 m +a. s. l. + +; + +9 May 2021 + +; +Anh D. Nguyen +leg.; bushes; IEBR-Myr 904 H + +. + + + +Paratypes + +. + +Vietnam +• +10 males +, +5 females +; same data as for holotype; EBR-Myr 904 P + +• + +1 male +, +1 female +; same data as for holotype; IEBR-Myr 901 + +. + + + + +Diagnosis. + +The species can be discriminated from the congeners by the presence of long spiniform paraterga, midbody metaterga with only two rows of 1 + 1 small setiferous spines in the middle and 2 + 2 longer setiferous spines near posterior margin; male femora 6 with a large tubercle ventrally; sternite 5 with a large, sparsely setose, bifid, trapeziform lamina between male coxae 4; epiproct without conspicuous setiferous knobs near tip; gonopod lamina lateralis broadly rounded, partly folded to sheathe distal part of solenomere; gonopod lamina medialis with a small rounded lobe at middle. + +The new species is similar to + +Hylomus namek +Nguyen et al., 2019 + +but differs from this species by the following characters: the ventral side of male femora 6 with a big, robust tubercle in the middle (vs. femora 6 and 7 with large tubercles); longer spiniform paraterga; and gonopod lamina medialis with a small rounded lobe in the middle (vs. without processes). + + + + +Etymology. + + +The name refers to + +“ +piccolo + +”, a main character of the Japanese manga “ Dragon balls ” by Toriyama Akira ( +Japan +). Noun in apposition. + + + + +Description. + + +Length c. +11.6–12.8 mm +(male), +13.9–15.2 mm +(female); width of midbody pro- and metazona (distance between two paratergal tips) +0.6–0.8 mm +(male), +1.12–1.25 mm +(female) and +3.1–3.3 mm +(male), +3.4–3.6 mm +(female), respectively. +Holotype +length c. +11.8 mm +, width of midbody pro- and metazona +0.74 mm +and +3.2 mm +, respectively. + + +Coloration +: Generally darkish-red to darkish-brown except paraterga, sterna, legs whitish-yellow; distal part of main branch pinkish. + + +Head +(Fig. +1 A – C +): Clypeolabral region densely setose, vertex sparsely setose. Epicranial suture distinct, dividing frons into two equal parts; with setae along the suture. Antenna slender, extremely long, reaching back to body ring 7 if stretched along the body axis; antennomere 1 <7 <6 <2 <3 = 4 = +5 in +length. + + + + + + +. + +Hylomus piccolo + +sp. nov. +, holotype (IEBR-Myr 904 H) +A, B +anterior-most body part, lateral view ( +A +), ventral view ( +B +) +C +head, anterior view +D +body rings 8–10, dorsal view. Scale bars: 1 mm. + + + +Collum +(Fig. +1 C +): Slightly narrower than head; surface dull, coarsely microgranulate; with two rows of spines: 3 + 3 spines in anterior row and 2 + 2 spines in posterior row. Paraterga of collum well developed, spiniform; directed dorsad; highly elevated above dorsal surface; with two conspicuous teeth on anterior side. + + +Body rings +: Ring 3 <4 <2 = +5–16 in +width, thereafter gradually tapering towards telson. Prozona finely shagreened; metazona and pleura with microgranulations. Transverse sulcus present, but inconspicuous on metaterga 5–18. Axial line missing. Metaterga with two rows of 1 + 1 smaller setiferous spines in middle and 2 + 2 longer setiferous spines near posterior margin (Fig. +2 B +). Suture between pro- and metazona broad, very shallow. Pleurosternal carinae present as a complete keel on body rings 2–3, then missing on subsequent body rings. + + + + + + + +Hylomus piccolo + +sp. nov. +, holotype (IEBR-Myr 904 H) +A +body rings 8–10, lateral view +B +body ring 10, dorsal view (under UV light) +C +body rings 8–10, ventral view +D +posterior-most body part, dorsal view. Scale bars: 1 mm. + + + +Paraterga +(Figs +1 +, +2 +): Very well developed; directed dorsad; long and spiniform with a large branch and 2–3 tiny teeth on anterior side (2 on poreless body rings and 3 on pore-bearing rings) and with 1 larger spine on posterior side. Paratergum on ring 19 directed caudad. Ozopore located between the second tooth and main branch of paraterga, visible in dorsal view. + + +Telson +(Fig. +3 A, B +): Epiproct without conspicuous setiferous knobs near tip, but broadly truncated; tip with four spinnerets; lateral tubercles well developed (Fig. +3 A +). Hypoproct subtrapeziform, with two distolateral, completely separated, setiferous knobs (Fig. +3 B +). + + + + + + + +Hylomus piccolo + +sp. nov. +, holotype (IEBR-Myr 904 H) +A +telson, dorsal view +B +telson, ventral view (under UV light) +C +leg 6 +D +sternum 5, subposterior view (under UV light). Scale bars: 1 mm. + + + +Legs +: Extremely long, slender and thin, c. 1.8–2.0 times as long as midbody height. Prefemora not swollen. Male femora 6 each ventrally with a large, robust tubercle in middle (Figs +1 A +, +3 C +). + + +Sterna +: With distinct cross-impressions, no modification – except a large, sparsely setose, bifid, trapeziform lamina between male coxae 4 (Figs +1 A +, +3 D +). + + +Gonopod +(Fig. +4 +): Suberect. Coxite ( +co +) cylindrical, larger than femorite, sparsely setose distodorsally. Prefemorite ( +pref +) densely setose, equal to femorite as well. Femorite ( +fe +) slightly enlarged distad (from ventral view); without a demarcation with postfemoral region. Postfemoral region inconspicuous. Solenophore ( +sph +) well developed; lamina lateralis ( +ll +) broadly rounded, partly folded to sheathe distal part of solenomere; lamina medialis ( +lm +) with a small rounded lobe at about midway. Seminal groove running entirely on mesal side, then entering a flagelliform solenomere ( +sl +), solenomere partly sheathed by solenophore. Tip of solenophore rounded. + + + + + + + +Hylomus piccolo + +sp. nov. +, holotype (IEBR-Myr 904 H), +SEM +A – D +left gonopod, lateral view ( +A +), dorsal view ( +B +), ventral view ( +C +), mesal view ( +D +) +E – H +distal part of left gonopod, lateral view ( +E +), dorsal view ( +F +), ventral view ( +G +), mesal view ( +H +). Abbreviations: +co += coxite; +pref += prefemorite; +fe += femorite; +ca += canula; +lm += lamina medialis; +ll += lamina lateralis; +sl += solenomere. Scale bars: 200 µm ( +A – D +); 100 µm ( +E – G +); 50 µm ( +H +). + + + + + +DNA barcoding. + + +(Appendix +1 +) A fragment of the +COI +gene is accessioned at +NCBI +GenBank with the following accession number +PQ 676351 +. The new species exhibits a +COI +gene similarity of 86.22 % and 86.57 % ( +OR 765910 +and + + +MG +669370 + + +, respectively) identity with + +Hylomus cervarius +( +Attems, 1953 +) + +. + + + + \ No newline at end of file diff --git a/data/A4/6C/59/A46C5981898F53AFA9BA5002BB19AC85.xml b/data/A4/6C/59/A46C5981898F53AFA9BA5002BB19AC85.xml new file mode 100644 index 00000000000..fce566a4ca9 --- /dev/null +++ b/data/A4/6C/59/A46C5981898F53AFA9BA5002BB19AC85.xml @@ -0,0 +1,317 @@ + + + +Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species + + + +Author + +Ham, Daseul +0000-0002-1900-3637 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea & Species Diversity Research Division, Biodiversity Research Department, National Institute of Biological Resources, Incheon, Republic of Korea + + + +Author + +Bae, Yeon Jae +0000-0001-7810-5409 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea + +text + + +ZooKeys + + +2025 + +2025-01-09 + + +1223 + + +221 +245 + + + +journal article +10.3897/zookeys.1223.128062 +731a7009-110a-4454-838b-7a8f9e4954bb + + + + + +Campylomyza aborigena +Mamaev, 1998 + + + + + +Fig. 1 C +, +2 A – C + + + + + + + +Campylomyza aborigena + +Mamaev, 1998: 6 +. + + + + + + + + +Specimens examined. + + + +Korea +• +1 ♂ +(slide no. +NIBRIN 0000992639 +); + + +Sobaek + + +; + +6 May – 6 Jun. 2019 + +; +D. Ham +, +S. Park +leg.; deposited in + +NIBR + + +• + +2 ♂♂ +(slides no. +NIBRIN 0000992638 +, +19-38 +); + +Odae +2 + +; + +23 Apr. – 11 May 2019 + +; +D. Ham +, +S. Park +leg.; deposited in + +NIBR + + +. + + + + +Diagnosis. + + + +Campylomyza aborigena + +closely resembles + +C. aemula +Mamaev, 1998 + +(inferred from the illustration in +Jaschhof and Jaschhof 2009 +) and shares the following characteristics: 1) Tegmen with lamellate (Fig. +2 C +, ↓ +5 +), tapering apical points that are rounded and strongly sclerotized anteriorly, and weakly sclerotized posteriorly; 2) Large foliate dorsal processes (Fig. +2 C +, ↓ +6 +) with narrower, sharp points; 3) Gonostyli tapering apically and curved anteroventrally with convex apex margins (Fig. +2 B +). However, + +C. aborigena + +can be distinguished from + +C. aemula + +by the following characteristics: tegmen with parallel-sided apical points (Fig. +2 C +, ↓ +5 +); dorsal processes large, broad basally, pointed apically with strongly sclerotized margin (Fig. +2 C +, ↓ +6 +). + + + + +Measurements. + + +Male adult (Slide no. +NIBRIN +0000992639): Body length +1.454 mm +. Wing length +1.484 mm +. Hind leg coxa +0.170 mm +; femur +0.547 mm +; tibia +0.551 mm +; tarsomere I +0.307 mm +; tarsomere II +0.164 mm +; tarsomere III +0.130 mm +; tarsomere IV +0.067 mm +; tarsomere +V +0.062 mm +. + + + + +Redescription. + + +Male adult. + +Head +. + +Postocular bristles four or five. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomeres as long as node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. + +Thorax +. + +Preepisternum with eight setae. Wing length to width ratio 2.44, AntC ending beyond +R +4 + 5 +but before reaching M +4 +; ApicR +1 +3.23 × length of Rs; CuA separated (Fig. +1 C +). Tarsomere I longer than tarsomere II. Claws sickle-shaped, toothed; empodia longer than claws; pubescent. + +Terminalia +. + +Tg 9 slightly tapered towards apex (Fig. +2 A +, ↓ +1 +). Gonocoxites emarginated broad U-shaped ventrally. (Fig. +2 A +, ↓ +2 +); ventromedial portion swollen, pronounced (Fig. +2 A +, ↓ +3 +); dorsal transverse bridge narrower to apex, extending far beyond ventrobasal margin (Fig. +2 A +, ↓ +4 +). Gonostyli curved anteroventrally; apical margin strongly convex; medial portion excavated; setae becoming denser towards apex. On tegmen, apical points long, lamellate, rounded apically (Fig. +2 C +, ↓ +5 +); dorsal processes spoon-shaped with hollow in the center and strongly sclerotized apex; directed anteriorly (Fig. +2 C +, ↓ +6 +). Mesal processes short, sclerotized (Fig. +2 C +, ↓ +7 +). Tegmen shoulders inconspicuous. + + + + +Distribution. + + +Russia +( +Primorsky +), new to +South Korea +. + + + + +Remarks. + + + +Campylomyza aborigena +Mamaev, 1998 + +was originally described based on a single specimen collected in Far East +Russia +in 1964. Mamaev’s description was limited to just seven lines of text, without any accompanying drawings or photographs. However, thanks to the observations made by Dr. Mathias Jaschhof on the +holotype +specimen of + +C. aborigena + +in the Zoological Museum of +Moscow State +University in 2006, we now know that the Korean species is the same as the Russian + +C. aborigena + +. This is significant because it provides further evidence supporting the existence of + +C. aborigena + +, with the Korean finding being only the second record except for the +holotype +. Mamaev often described species based on a single specimen without proper illustration or depiction. Therefore, the discovery of this species in +Korea +and the possibility of obtaining additional specimens are of great importance for further supporting Mamaev’s species concept and advancing the taxonomy of mycophagous cecidomyiids. + + + + \ No newline at end of file diff --git a/data/AC/7C/74/AC7C741F6FBB5CE884AFFC6BEB07096E.xml b/data/AC/7C/74/AC7C741F6FBB5CE884AFFC6BEB07096E.xml new file mode 100644 index 00000000000..4e5c8d4ac44 --- /dev/null +++ b/data/AC/7C/74/AC7C741F6FBB5CE884AFFC6BEB07096E.xml @@ -0,0 +1,131 @@ + + + +Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species + + + +Author + +Ham, Daseul +0000-0002-1900-3637 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea & Species Diversity Research Division, Biodiversity Research Department, National Institute of Biological Resources, Incheon, Republic of Korea + + + +Author + +Bae, Yeon Jae +0000-0001-7810-5409 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea + +text + + +ZooKeys + + +2025 + +2025-01-09 + + +1223 + + +221 +245 + + + +journal article +10.3897/zookeys.1223.128062 +731a7009-110a-4454-838b-7a8f9e4954bb + + + + +Genus + +Campylomyza +Meigen, 1818 + + + + + +Fig. 1 C + + + + + + + +Campylomyza + +Meigen, 1818: 101 +; + +Westwood 1840: 126 + +; + + +Jaschhof 1998 b + +: 136 + +; + +Jaschhof and Jaschhof 2009: 89 + +. + + + + + + + + + +Type +species. + + + + +Campylomyza flavipes +Meigen, 1818 + +(original designation by +Westwood 1840 +). +Type +locality +Germany +. + + + + +Diagnosis. + + +The adult males of the South Korean genus + +Campylomyza + +can be distinguished from other mycophagous cecidomyiid taxa based on the following combination of characters [adapted from +Jaschhof and Jaschhof 2009 +]: 1) Antenna with 12 flagellomeres; 2) Node of fourth antennal flagellomere featuring one complete and two incomplete crenulate whorls with sensory hairs with two incompletely collar-shaped sensilla distally; 3) Apical part of the +R +1 +vein, located near wing tip (ApicR +1 +) elongated, approximately 4–6 times the length of Rs; 4) Gonostyli strongly convex posteriorly without apical spines; 5) Aedeagal apodeme equipped with typical head-like structure; 6) Tegmen with transverse brace (i. e., H-shaped), various processes on apex. + + + + \ No newline at end of file diff --git a/data/AD/63/65/AD6365B292675E2AB330779926A0ACEC.xml b/data/AD/63/65/AD6365B292675E2AB330779926A0ACEC.xml new file mode 100644 index 00000000000..5f9ee2a465b --- /dev/null +++ b/data/AD/63/65/AD6365B292675E2AB330779926A0ACEC.xml @@ -0,0 +1,123 @@ + + + +Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species + + + +Author + +Ham, Daseul +0000-0002-1900-3637 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea & Species Diversity Research Division, Biodiversity Research Department, National Institute of Biological Resources, Incheon, Republic of Korea + + + +Author + +Bae, Yeon Jae +0000-0001-7810-5409 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea + +text + + +ZooKeys + + +2025 + +2025-01-09 + + +1223 + + +221 +245 + + + +journal article +10.3897/zookeys.1223.128062 +731a7009-110a-4454-838b-7a8f9e4954bb + + + + + +Campylomyza cavitata +Mamaev, 1998 + + + + + + + + +Campylomyza cavitata + +Mamaev, 1998: 7 +; + +Jaschhof and Jaschhof 2009: 112–113 + +, fig. 37 A – C. + + + + + + + + +Specimens examined. + + + +Korea +• +1 ♂ +(slide no. +NIBR 0000919409 +); + +Odae +1 + +; + +11–26 May 2019 + +; +D. Ham +, +S. Park +leg.; deposited in + +NIBR + + +. + + + + +Distribution. + + +Sweden +, +Finland +, +Germany +, +Russia +, new record for +South Korea +. + + + + \ No newline at end of file diff --git a/data/CB/1B/5D/CB1B5D206DA25D84B9D4EBA6F558C1CB.xml b/data/CB/1B/5D/CB1B5D206DA25D84B9D4EBA6F558C1CB.xml new file mode 100644 index 00000000000..e1b948cf06c --- /dev/null +++ b/data/CB/1B/5D/CB1B5D206DA25D84B9D4EBA6F558C1CB.xml @@ -0,0 +1,114 @@ + + + +Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species + + + +Author + +Ham, Daseul +0000-0002-1900-3637 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea & Species Diversity Research Division, Biodiversity Research Department, National Institute of Biological Resources, Incheon, Republic of Korea + + + +Author + +Bae, Yeon Jae +0000-0001-7810-5409 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea + +text + + +ZooKeys + + +2025 + +2025-01-09 + + +1223 + + +221 +245 + + + +journal article +10.3897/zookeys.1223.128062 +731a7009-110a-4454-838b-7a8f9e4954bb + + + + + +Campylomyza cingulata +Jaschhof, 2009 + + + + + + + + +Campylomyza cingulata + +Jaschhof, 2009: 119 +, fig. 41 A – E. + + + + + + + + +Specimens examined. + + + +Korea +• +1 ♂ +(slide no. +NIBRIN 0000941946 +); + +Odae +1 + +; + +18 Apr. – 1 May 2020 + +; +D. Ham +, +S. Park +leg.; deposited in + +NIBR + + +. + + + + +Distribution. + + +Fennoscandia, +Germany +, new record for +South Korea +. + + + + \ No newline at end of file diff --git a/data/D7/17/8C/D7178C0065385A48BF28E24F28153231.xml b/data/D7/17/8C/D7178C0065385A48BF28E24F28153231.xml new file mode 100644 index 00000000000..329cc0588a7 --- /dev/null +++ b/data/D7/17/8C/D7178C0065385A48BF28E24F28153231.xml @@ -0,0 +1,275 @@ + + + +Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species + + + +Author + +Ham, Daseul +0000-0002-1900-3637 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea & Species Diversity Research Division, Biodiversity Research Department, National Institute of Biological Resources, Incheon, Republic of Korea + + + +Author + +Bae, Yeon Jae +0000-0001-7810-5409 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea + +text + + +ZooKeys + + +2025 + +2025-01-09 + + +1223 + + +221 +245 + + + +journal article +10.3897/zookeys.1223.128062 +731a7009-110a-4454-838b-7a8f9e4954bb + + + + + +Campylomyza angusta + +sp. nov. + + + + +Fig. 3 A – C + + + + +Type material examined. + + + + +Holotype + +: +Korea +• +1 ♂ +(slide no. +NIBRIN 0000941947 +); +Gangwon-do +, +Pyeongchang-gun +, +Jinbu-myeon +, +Odaesan-ro +, +Mt. Odae +, small valley before +So-Myeong valley +(Odae 1) +; + +18 Apr. – 1 May 2020 + +; +D. Ham +, +S. Park +leg.; deposited in + +NIBR + +. + + + + + +Diagnosis. + + + +Campylomyza angusta + +sp. nov. +belongs to the +ormerodi +group of species where it is reminiscent of + +C. pubescens +( +Jaschhof and Jaschhof 2009 +) + +mainly due to cerci bearing strikingly large pubescence and short dorsal transverse bridge, which is almost not protruding beyond the ventrobasal margin. + +Campylomyza angusta + +sp. nov. +is distinguished as follows. Gonostyli moderately convex posteriorly with narrowly rounded apex (Fig. +3 A +, ↓ +6 +). Gonocoxites strongly protruding dorsomedially, ventral bridge short. The tegmen lacks shoulders (Fig. +3 C +, ↓ +4 +), parameral apodemes long (Fig. +3 C +, ↓ +5 +), apical points directed slightly laterally, mesal points short, weakly sclerotized, rounded apically (Fig. +3 C +, ↓ +3 +). + + + + + + +Male morphology of + +Campylomyza angusta + +sp. nov. +, holotype +A – C +and + +Campylomyza convexa + +sp. nov. +, holotype +D – F +: +A +gonocoxites, ventral veiw +B +gonostylus, dorsal view +C +tegmen, dorsal view +D +gonocoxites, ventral veiw +E +gonostylus, dorsal view +F +tegmen, dorsal view. Scale bars: 0.05 mm. + + + + + +Measurements. + + +Male adult ( +holotype +): Body length +1.329 mm +. Wing length +1.569 mm +. Hind leg coxa +0.160 mm +; femur +0.571 mm +; tibia +0.567 mm +; tarsomere I +0.330 mm +; tarsomere II +0.153 mm +; tarsomere III +0.109 mm +; tarsomere IV +0.078 mm +; tarsomere +V +0.061 mm +. + + + + +Description. + + +Male adult ( +holotype +). + +Head +. + +Postocular bristles seven. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomeres shorter than node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. + +Thorax +. + +Preepisternum with eight setae. Wing length to width ratio 2.53. AntC ending beyond +R +4 + 5 +but before reaching M +4 +; ApicR +1 +4.18 × length of Rs. CuA separated. Tarsomere I longer than tarsomere II. Claws sickle-shaped, fine toothed; empodia shorter than claws; pubescent. + +Terminalia +. + +Tg 9 tapered towards apex with 13 setae apically. Ventral bridge of gonocoxites short, dorsal transverse bridge protruding only slightly beyond the ventrobasal margin. Ventral emargination deep, U-shaped. Ventromedial portion broad rounded, not protruding medially (Fig. +3 A +, ↓ +1 +). Gonostyli rounded apically with semi-circular apical margin; excavated ventromedially, plump dorsally; setae denser towards apex. On tegmen, apical points not lamellate, pointed apically, directed slightly posterolaterally (Fig. +3 C +, ↓ +2 +); mesal points weakly sclerotized, short, tapered basally, broadened at apical third, rounded apically (Fig. +3 C +, ↓ +3 +). Tegmen shoulders indistinct (Fig. +3 C +, ↓ +4 +). Parameral apodemes long, more than half-length of tegmen (Fig. +3 C +, ↓ +5 +). + + + + +Etymology. + + +The specific epithet + +angusta + +in Latin means narrow, referring to the narrowness of the shoulder region of the tegmen in this species. + + + + \ No newline at end of file diff --git a/data/FB/7F/0A/FB7F0A266D625ECEBE3EC29C56C9E0FF.xml b/data/FB/7F/0A/FB7F0A266D625ECEBE3EC29C56C9E0FF.xml new file mode 100644 index 00000000000..1c58b33031f --- /dev/null +++ b/data/FB/7F/0A/FB7F0A266D625ECEBE3EC29C56C9E0FF.xml @@ -0,0 +1,277 @@ + + + +Taxonomic study of the genus Campylomyza Meigen (Diptera, Cecidomyiidae) in Korea with descriptions of seven new species + + + +Author + +Ham, Daseul +0000-0002-1900-3637 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea & Species Diversity Research Division, Biodiversity Research Department, National Institute of Biological Resources, Incheon, Republic of Korea + + + +Author + +Bae, Yeon Jae +0000-0001-7810-5409 +Department of Environmental Science and Ecological Engineering, Graduate School, Korea University, Seoul, Republic of Korea + +text + + +ZooKeys + + +2025 + +2025-01-09 + + +1223 + + +221 +245 + + + +journal article +10.3897/zookeys.1223.128062 +731a7009-110a-4454-838b-7a8f9e4954bb + + + + + +Campylomyza odae + +sp. nov. + + + + +Fig. 5 A – D + + + + +Type material examined. + + + + +Holotype + +: +Korea +• +1 ♂ +(slide no. +NIBRIN 0000992641 +) Gangwon-do, Pyeongchang-gun, Jinbu-myeon, Odaesan-ro, +Mt. Odae +, the road before temple (Buk-Dae-Mi-Reuk-Am) +(Odae 2) +; + +11–26 May 2019 + +; +D. Ham +, +S. Park +leg.; deposited in + +NIBR + + +. + + +Paratype + +: +Korea + +• + +1 ♂ +(slide no. +NIBRIN 0000919408 +); same data and deposition as +holotype + +. + + + + +Diagnosis. + + + +Campylomyza odae + +sp. nov. +is distinguishable from other + +Campylomyza +species + +by the following combination of characteristics: 1) Apical margin of gonostyli rounded (Fig. +5 A +, ↓ +3 +); 2) Dorsal processes on tegmen with inconspicuous pair of subtriangular processes anterolaterally; 3) Dorsal processes constricted medially, forming mesal cleft (Fig. +5 C +, ↓ +6 +); 4) Cerci visible (Fig. +5 D +). + + + + + + +Male morphology of + +Campylomyza odae + +sp. nov. +, holotype +A – D +and + +Campylomyza salicia + +sp. nov. +, holotype +E – G +: +A +gonocoxites, ventral view +B +gonostylus, dorsal view +C +tegmen, dorsal view +D +cerci, ventral view +E +gonocoxites, ventral view +F +gonostylus, dorsal view +G +tegmen, dorsal view. Scale bar: 0.05 mm. + + + + + +Measurements. + + +Male adult ( +Holotype +): Body length +1.737 mm +. Wing length +1.870 mm +. Hind leg coxa +0.221 mm +; femur +0.713 mm +; tibia +0.624 mm +; tarsomere I +0.369 mm +; tarsomere II +0.193 mm +; tarsomere III +0.134 mm +; tarsomere IV +0.089 mm +; tarsomere +V +0.072 mm +. + + + + +Description. + + +Male adult. Slightly larger than other + +Campylomyza +species. + + +Head +. + +Postocular bristles four. Antenna with 12 flagellomeres. Neck of fourth antennal flagellomere slightly shorter than node. Node with one complete and two incomplete crenulate whorls with sensory hairs, two incompletely collar-shaped sensilla distally. Palpus 4 - segmented; fourth segment longest. + +Thorax +. + +Wing length to width ratio 2.39, AntC ending beyond +R +4 + 5 +but before reaching M +4 +; ApicR +1 +4.31 × length of Rs; CuA separated. Tarsomere I longer than tarsomere II. Claws sickle-shaped, toothed; empodia small, shorter than claws. + +Terminalia +. + +Tg 9 broadly tapered towards apex with eight fine setae. Ventral emargiantion U-shaped; ventral bridge long; dorsal transverse bridge extending far beyond ventrobasal margin (Fig. +5 A +, ↓ +1 +); ventromedial portion of gonocoxites relatively narrow, not pronounced (Fig. +5 A +, ↓ +2 +). Gonostyli short, stout, strongly convex posteriorly, truncated apically (Fig. +5 A +, ↓ +3 +), directed ventrally, bearing dorsoapically numerous straight setae of various length, with denser stiff setae as it goes to apex. Tegmen narrow, shoulders inconspicuous. Parameral apodemes short. Apical points lamellated, triangular-shaped, directed posteriorly (Fig. +5 C +, ↓ +4 +), separated by wide cleft mesally; dorsal processes subtriangular shaped, directed dorsomedially, apices crossed with spreading subtriangular extensions (Fig. +5 C +, ↓ +5 +); each dorsal process constricted at midlength, forming mesal cleft (Fig. +5 C +, ↓ +6 +). Cerci visible. + + + + +Etymology. + + +The species name + +odae + +is a noun in apposition to the collection locality, Mt. Odae in +Gangwon province +. + + + + \ No newline at end of file