From 3a9a4563a3928b2557e7aac2a6bf8afe9675d5ce Mon Sep 17 00:00:00 2001 From: ggserver Date: Thu, 12 Dec 2024 18:25:17 +0000 Subject: [PATCH] Add updates up until 2024-12-12 18:19:42 --- .../87/03C387E4FFF3FFBBFD83FE9B14A7FE6F.xml | 162 +++--- .../16/03C8165E34384914980A84840D2D3499.xml | 442 ++++++++++++++++ .../16/03C8165E343B49129BCB86A60B7531BD.xml | 124 ++--- .../87/737287D7FFBEEC29FDB0FE24FB35F81A.xml | 495 ++++++++++++++++++ 4 files changed, 1082 insertions(+), 141 deletions(-) create mode 100644 data/03/C8/16/03C8165E34384914980A84840D2D3499.xml create mode 100644 data/73/72/87/737287D7FFBEEC29FDB0FE24FB35F81A.xml diff --git a/data/03/C3/87/03C387E4FFF3FFBBFD83FE9B14A7FE6F.xml b/data/03/C3/87/03C387E4FFF3FFBBFD83FE9B14A7FE6F.xml index caf639fa219..ba4365be333 100644 --- a/data/03/C3/87/03C387E4FFF3FFBBFD83FE9B14A7FE6F.xml +++ b/data/03/C3/87/03C387E4FFF3FFBBFD83FE9B14A7FE6F.xml @@ -1,98 +1,100 @@ - - - -A new species of Knodus (Characiformes: Characidae), with deep genetic divergence, from the Mearim and Munim river basins, Northeastern Brazil, and evidence for hidden diversity in adjacent river basins + + + +A new species of Knodus (Characiformes: Characidae), with deep genetic divergence, from the Mearim and Munim river basins, Northeastern Brazil, and evidence for hidden diversity in adjacent river basins - - -Author + + +Author -Aguiar, Rayane G. +Aguiar, Rayane G. - - -Author + + +Author -Guimarães, Erick C. -Universidade Federal do Oeste do Pará, Programa de Pós-Graduação Sociedade Natureza e Desenvolvimento, Instituto de Ciências da Educação, Av. Mendonça Furtado, 2946, Fátima, 68040 - 470 Santarém, PA, Brazil. erick. ictio @ yahoo. com. br (corresponding author). & Universidade Estadual do Maranhão, Laboratório de Ictiofauna e Piscicultura Integrada, Centro de Ciências Agrárias, Cidade Universitária Paulo VI, 65055 - 310 São LuÍs, MA, Brazil. (JPS) jadsonsantos @ professor. uema. br. +Guimarães, Erick C. +Universidade Federal do Oeste do Pará, Programa de Pós-Graduação Sociedade Natureza e Desenvolvimento, Instituto de Ciências da Educação, Av. Mendonça Furtado, 2946, Fátima, 68040 - 470 Santarém, PA, Brazil. erick. ictio @ yahoo. com. br (corresponding author). & Universidade Estadual do Maranhão, Laboratório de Ictiofauna e Piscicultura Integrada, Centro de Ciências Agrárias, Cidade Universitária Paulo VI, 65055 - 310 São LuÍs, MA, Brazil. (JPS) jadsonsantos @ professor. uema. br. - - -Author + + +Author -Brito, Pâmella S. de +Brito, Pâmella S. de - - -Author + + +Author -Santos, Jadson P. -Universidade Estadual do Maranhão, Laboratório de Ictiofauna e Piscicultura Integrada, Centro de Ciências Agrárias, Cidade Universitária Paulo VI, 65055 - 310 São LuÍs, MA, Brazil. (JPS) jadsonsantos @ professor. uema. br. +Santos, Jadson P. +Universidade Estadual do Maranhão, Laboratório de Ictiofauna e Piscicultura Integrada, Centro de Ciências Agrárias, Cidade Universitária Paulo VI, 65055 - 310 São LuÍs, MA, Brazil. (JPS) jadsonsantos @ professor. uema. br. - - -Author + + +Author -Katz, Axel M. -Universidade Federal do Rio de Janeiro, Laboratório de Sistemática e Evolução de Peixes Teleósteos, Departamento de Zoologia, Instituto de Biologia, Cidade Universitária, 21941 - 599 Rio de Janeiro, RJ, Brazil. axelmk @ gmail. com. & S / N, Boa Vista, 65500 - 000 Chapadinha, MA, Brazil. fpottoni @ gmail. com. -Brazil.axelmk@gmail.com +Katz, Axel M. +Universidade Federal do Rio de Janeiro, Laboratório de Sistemática e Evolução de Peixes Teleósteos, Departamento de Zoologia, Instituto de Biologia, Cidade Universitária, 21941 - 599 Rio de Janeiro, RJ, Brazil. axelmk @ gmail. com. & S / N, Boa Vista, 65500 - 000 Chapadinha, MA, Brazil. fpottoni @ gmail. com. +Brazil.axelmk@gmail.com - - -Author + + +Author -Dias, Luiz Jorge B. da S. -Universidade Estadual do Maranhão, Centro de Educação, Ciências Exatas e Naturais. Cidade Universitária Paulo VI, Tirirical 65055 - 970 São LuÍs, MA, Brazil. luizjorgedias @ hotmail. com. -Brazil.luizjorgedias@hotmail.com +Dias, Luiz Jorge B. da S. +Universidade Estadual do Maranhão, Centro de Educação, Ciências Exatas e Naturais. Cidade Universitária Paulo VI, Tirirical 65055 - 970 São LuÍs, MA, Brazil. luizjorgedias @ hotmail. com. +Brazil.luizjorgedias@hotmail.com - - -Author + + +Author -Carvalho-Costa, Luis Fernando +Carvalho-Costa, Luis Fernando - - -Author + + +Author -Ottoni, Felipe P. -Universidade Federal do Maranhão, Centro de Ciências Agrárias e Ambientais, Laboratório de Sistemática e Ecologia de Organismos Aquáticos, Campus de Chapadinha, BR- 222, km +Ottoni, Felipe P. +Universidade Federal do Maranhão, Centro de Ciências Agrárias e Ambientais, Laboratório de Sistemática e Ecologia de Organismos Aquáticos, Campus de Chapadinha, BR- 222, km -text - - -Neotropical Ichthyology +text + + +Neotropical Ichthyology - -2022 - -e 210173 + +2022 + +e 210173 - -2022-06-03 + +2022-06-03 - -20 + +20 - -2 + +2 - -1 -27 + +1 +27 - -http://dx.doi.org/10.1590/1982-0224-2021-0173 + +http://dx.doi.org/10.1590/1982-0224-2021-0173 -journal article -10.1590/1982-0224-2021-0173 -1982-0224 -13350457 -BE91D7F5-F56D-40B3-AA1D-A9C974083BC6 +journal article +306428 +10.1590/1982-0224-2021-0173 +19a65529-737c-419b-beff-d6d51d0f697a +1982-0224 +13350457 +BE91D7F5-F56D-40B3-AA1D-A9C974083BC6 - + @@ -114,7 +116,7 @@ urn:lsid:zoobank.org:act: ( Figs. 1–3 ; -Tabs. 2–3 +Tabs. 2–3 ) @@ -190,7 +192,7 @@ CICCAA 1518, 22.8 mm SL, Brazil, Maranhão, Alto Alegre do Pindaré municipality CICCAA 2696, 40.2 mm SL, Brazil, Maranhão, Chapadinha municipality, stream in riparian forest on the road BR–222, Munim River basin. - + TABLE 1 | Specimens and DNA sequence information included in the study. Sequences made available by this study follow with asteristic. @@ -1768,7 +1770,7 @@ Maxilla. Dentary. Scale bar = 1 mm. - + TABLE 2 | Morphometric data (N = 110) of the holotype and paratypes of @@ -2039,7 +2041,7 @@ from the Mearim River basin. SD = Standard deviation. - + TABLE 3 | Morphometric data (N = 136) for the paratypes of @@ -2608,7 +2610,7 @@ by having more total vertebrae 33–35, mode 34 ( Description. Morphometric data presented in -Tabs. 2–3 +Tabs. 2–3 . Body comparatively small, with largest specimen examined measuring 37.7 mm SL. Greatest body depth at dorsal-fin origin. Dorsal profile of head convex from upper lip to vertical through middle portion of eye; slightly concave from this point to tip of supraoccipital spine; straight to slightly convex from posterior tip of supraoccipital spine to dorsal-fin origin; dorsal-fin base straight; slightly convex to straight from end of dorsal-fin base to adipose fin and concave from latter point to anterior dorsal-procurrent ray. Ventral profile of body convex from lower lip to anal-fin origin; straight, posterodorsally inclined along anal-fin base. Dorsal and ventral profile of caudal peduncle slightly concave. @@ -2729,7 +2731,7 @@ The genetic distance between the new species and victoriae is 13% ( -Tab. 4 +Tab. 4 ). @@ -2756,7 +2758,7 @@ Geographical distribution of . - + FIGURE 6 | Bayesian Inference phylogenetic tree generated by this study. The results of GMYC, bPTP and ABGD are included. Numbers above and below branches are posterior probability values. The gray bars correspond to the congruent results of the different species delimitation methods (Con.). @@ -2775,7 +2777,7 @@ species species ( -Fig. 6 +Fig. 6 ). One of the 17 lineages of Knodus @@ -2785,7 +2787,7 @@ represents the new species described herein ( Knodus guajajara ) with haplotypes from the Mearim and Munim river basins forming an exclusive clade supported by the highest possible support value (PP = 1) ( -Fig. 6 +Fig. 6 ). The BI phylogenetic analysis also delimited new lineages of Knodus @@ -2856,7 +2858,7 @@ cf. (Itapecuru River basin) (PP = 1). - + TABLE 4 | Kimura-2-parameters pairwise genetic distances among species. @@ -3307,7 +3309,7 @@ aff. GMYC, bPTP and ABGD. The results of the three species delimitation methods (GMYC, bPTP, and ABGD) were congruent ( -Fig. 6 +Fig. 6 ), and all three delimited the same 19 lineages. Two of them are outgroups ( Bryconamericus @@ -3318,7 +3320,7 @@ species Knodus lineages (species) ( -Fig. 6 +Fig. 6 ). The new species herein described ( K. guajajara diff --git a/data/03/C8/16/03C8165E34384914980A84840D2D3499.xml b/data/03/C8/16/03C8165E34384914980A84840D2D3499.xml new file mode 100644 index 00000000000..948e9852818 --- /dev/null +++ b/data/03/C8/16/03C8165E34384914980A84840D2D3499.xml @@ -0,0 +1,442 @@ + + + +Description of Neblinichthys peniculatus, a new species of loricariid catfish from the río Paragua drainage of Venezuela + + + +Author + +Armbruster, Jonathan W. +Department of Biological Sciences and Auburn University Museum of Natural History, 331 Funchess, Auburn, AL 36849, USA. armbrjw @ auburn. edu +armbrjw@auburn.edu + + + +Author + +Taphorn, Donald C. +1822 N. Charles St., Belleville, IL, USA. taphorn @ gmail. com +taphorn@gmail.com + +text + + +Neotropical Ichthyology + + +2013 + +2013-03-31 + + +11 + + +1 + + +65 +72 + + + + +http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1679-62252013000100065&lng=en&tlng=en + +journal article +299539 +10.1590/S1679-62252013000100007 +3b46cedf-2daf-4ae3-acdb-85e3c94029e3 +1982-0224 +12652838 + + + + + +Key to the species of + +Neblinichthys + + + + + + + + + +1a. Four or more preadipose plates; 10 or fewer elongate cheek odontodes ................................................... + +........ +N. roraima + + + + +1b. Three or fewer preadipose plates, 20 or more elongate cheek odontodes ................................................................... 2 + + + + +2a. Abdomen with irregular gray spots and vermiculations on a dark background; no (occasionally one) odontodes on the exposed portion of the opercle; iris operculum absent, internares width 5.0-8.5% HL .............................................. 3 + + +2b. Abdomen usually white or with dark spots or short vermiculations on a light background; 10 or more odontodes on the exposed portion of the opercle, iris operculum present; internares width 7.6-15.5% HL ......... 4 + + + + +Fig. 1. +Distribution of + +Neblinichthys + +. Main drainages where the species are located indicated. Symbols may represent multiple localities. + + + + + +3a. Dorsal-fin base length 18.1-22.8% SL; dorsal-anal distance 13.7-18.3% SL, snout decreasing in steep arc just anterior to eyes and then flattening in area anterior of nares; adpressed dorsal fin not reaching anterior preadipose plate ...................................................................... + +N. brevibracchium + + + + + +Table 1. +Morphometric features of the heads as percentage of HL for + +Neblinichthys brevibracchium + +(N = 23, except SL, N = 29), + +N. echinasus + +(N = 3), + +N. pilosus + +(N = 6), + +N. roraima + +(N = 4), and + +N. yaravi + +(N = 8, except anal-fin spine L. and interorbital W., N = 7). Landmarks are the numbered landmarks in +Armbruster (2003) +. Some + +N. roraima + +have completely adnate barbels, giving a measurement of zero. Revised from + +Taphorn +et al +. (2010) + +where these measurements were inadvertently published as ratios of predorsal length. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
LandmarksFeature + +N. brevibracchium + + + +N. echinasus + + + +N. pilosus + +
RangeAvg. ± SDRangeAvg. ± SDRangeAvg. ± SD
5-7Head-eye L.34.0-40.736.4±1.433.0-38.636.2±2.938.0-42.339.4±1.6
4-5Orbit Dia.14.3-17.215.8±0.814.9-19.317.8±2.515.3-17.916.9±1.0
1-4Snout L.52.6-62.859.3±2.560.2-63.361.6±1.660.4-66.563.4±2.6
2-3Internares W.6.5-11.48.2±1.08.1-9.18.6±0.517.3-20.118.7±1.0
5-6Interorbital W.47.8-54.550.9±1.752.5-55.754.2±1.6--
7-12Head Dp.54.5-83.961.9±4.956.5-59.658.4±1.763.9-68.766.8±1.8
1-24Mouth L.47.8-61.753.8±3.356.8-57.857.4±0.548.2-61.554.5±4.8
21-22Mouth W.45.2-55.150.4±2.653.2-56.254.6±1.554.3-63.659.5±3.7
22-23Barbel L.1.1-4.43.0±0.91.9-2.92.3±0.55.3-10.17.6±1.7
25-26Dentary tooth cup L.10.9-17.514.7±1.411.4-16.413.5±2.717.8-22.019.4±1.6
27-28Premaxillary tooth cup L.10.9-16.713.6±1.410.7-13.612.5±1.616.1-18.917.3±1.0
+ + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
LandmarksFeature + +N. roraima + + + +N. yaravi + +
RangeAvg. ± SDRangeAvg. ± SD
5-7Head-eye L.34.2-41.939.7±3.733.7-38.637.1±1.5
4-5Orbit Dia.14.4-17.216.2±1.215.8-18.517.4±0.9
1-4Snout L.54.9-61.958.5±2.955.1-64.759.3±3.0
2-3Internares W.12.3-15.013.8±1.29.3-11.810.4±0.9
5-6Interorbital W.--48.0-56.252.8±2.7
7-12Head Dp.61.3-63.462.5±0.961.2-66.863.3±1.7
1-24Mouth L.49.6-64.054.9±6.351.4-61.354.3±3.5
21-22Mouth W.53.7-66.062.0±5.854.3-64.060.5±3.4
22-23Barbel L.0.0-4.31.8±2.21.7-3.62.7±0.6
25-26Dentary tooth cup L.17.5-25.320.4±3.416.7-19.317.6±0.9
27-28Premaxillary tooth cup L.19.4-24.621.0±2.414.9-20.116.5±1.7
+ + + +3b. Dorsal-fin base length 24.3-27.0% SL; dorsal-anal distance 11.9-12.5% SL, snout tapering shallowly and continuously from eyes to snout tip; adpressed dorsal fin reaching anterior preadipose plate .................................... + +N. echinasus + + + + + + + +4a. Usually four anal-fin rays (one examined with five), spots on fins small dashes confined to rays; six to seven columns of spots on caudal fin ................................................. + +N. yaravi + + + + +4b. Five anal-fin rays; spots on fins large and round, extending onto membranes; three to five bands or columns of spots on caudal fin .......................................................................... 5 + + + + + +5a. Caudal peduncle with dark blotches forming mottling; head usually with spots (absent in nuptial males); rectangular blotch at base of caudal fin; nuptial males with relatively short odontodes directed largely upwards (see discussion); internares width 10.5-12.4% HL; postanal length 28.5-30.6% SL ........................................................................ + +N.peniculatus + + + + + +5b. Caudal peduncle brown; head without spots; no rectangular blotch at base of caudal fin; nuptial males with very long odontodes directed anteriorly (see discussion); internares width 17.3-20.1% HL; postanal length 32.8-34.9% SL ................................................................................. + +N. pilosus + + + + + + + + \ No newline at end of file diff --git a/data/03/C8/16/03C8165E343B49129BCB86A60B7531BD.xml b/data/03/C8/16/03C8165E343B49129BCB86A60B7531BD.xml index f328323d887..4a055bc3497 100644 --- a/data/03/C8/16/03C8165E343B49129BCB86A60B7531BD.xml +++ b/data/03/C8/16/03C8165E343B49129BCB86A60B7531BD.xml @@ -1,70 +1,72 @@ - - - -Description of Neblinichthys peniculatus, a new species of loricariid catfish from the río Paragua drainage of Venezuela + + + +Description of Neblinichthys peniculatus, a new species of loricariid catfish from the río Paragua drainage of Venezuela - - -Author + + +Author -Armbruster, Jonathan W. -Department of Biological Sciences and Auburn University Museum of Natural History, 331 Funchess, Auburn, AL 36849, USA. armbrjw @ auburn. edu -armbrjw@auburn.edu +Armbruster, Jonathan W. +Department of Biological Sciences and Auburn University Museum of Natural History, 331 Funchess, Auburn, AL 36849, USA. armbrjw @ auburn. edu +armbrjw@auburn.edu - - -Author + + +Author -Taphorn, Donald C. -1822 N. Charles St., Belleville, IL, USA. taphorn @ gmail. com -taphorn@gmail.com +Taphorn, Donald C. +1822 N. Charles St., Belleville, IL, USA. taphorn @ gmail. com +taphorn@gmail.com -text - - -Neotropical Ichthyology +text + + +Neotropical Ichthyology - -2013 - -2013-03-31 + +2013 + +2013-03-31 - -11 + +11 - -1 + +1 - -65 -72 + +65 +72 - -http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1679-62252013000100065&lng=en&tlng=en + +http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1679-62252013000100065&lng=en&tlng=en -journal article -299539 -10.1590/S1679-62252013000100007 -3b46cedf-2daf-4ae3-acdb-85e3c94029e3 -1982-0224 -12652838 +journal article +299539 +10.1590/S1679-62252013000100007 +3b46cedf-2daf-4ae3-acdb-85e3c94029e3 +1982-0224 +12652838 - - + + Neblinichthys peniculatus , new species + + Figs. 2-4 , -Table 2 - +Table 2 + @@ -189,7 +191,7 @@ at third rapids above camp along left bank, Diagnosis. - + Neblinichthys peniculatus differs from all congeners by having mottling on the caudal peduncle consisting of dark spots and dashes ( @@ -207,17 +209,17 @@ and ), and by having hypertrophied snout odontodes smaller than orbit diameter ( vs. much larger than orbit diameter; nuptial males unknown for - + N. yaravi ; see Discussion, Fig. 3 ); from - + N. brevibracchium and - + N. echinasus by having an iris operculum ( @@ -227,21 +229,21 @@ operculum absent or at most dorsal rim of iris straight), by having odontodes on usually zero, but no more than one, odontodes on opercle), and internares 3.9-4.6% HL ( vs. 5.0- 8.5% in - + N. brevibracchium and 6.2-6.7% in - + N. echinasus ), and by having no spots (or at best very faint spots on a light background) on the abdomen of adult males ( vs. large light spots and vermiculations on a dark abdomen); from - + N. pilosus and - + N. yaravi by having a rectangular dark blotch at the base of the caudal fin ( @@ -251,7 +253,7 @@ blotch absent; and 4 ); from - + N. pilosus by internares width 10.5-12.4% HL ( @@ -259,7 +261,7 @@ by internares width 10.5-12.4% HL ( 17.3-20.1%), and postanal length 28.5-30.6% SL ( vs. 32.8- 34.9%); from - + N. roraima by having a one (occasionally two) preadipose plates with the adipose membrane conspicuous ( @@ -267,27 +269,27 @@ by having a one (occasionally two) preadipose plates with the adipose membrane c five to nine preadipose plates and the adipose membrane inconspicuous or absent), and greater than 20 evertible cheek odontodes ( vs. 10 or fewer); from - + N. roraima and - + N. yaravi by having five anal-fin rays ( vs. three to four in - + N. roraima and four, one specimen with five, in - + N. yaravi ); and from - + N. yaravi by having large spots on the fins that clearly proceed onto the membranes ( @@ -311,7 +313,7 @@ and Description. Morphometrics presented in -Table 1 +Table 1 . Meristics based on eight individuals. Largest specimen male: 81.3 mm SL. @@ -328,7 +330,7 @@ with two) preadipose plates. Caudal fin I,14,I; lower caudal-fin spine slightly Fig. 2. Dorsal, lateral, and ventral views of - + Neblinichthys peniculatus , holotype, male, MBUCV V-35680, 78.8 mm SL, Venezuela, Bolivar, río Paragua drainage, río Carapo at first rapids along right bank. @@ -338,7 +340,7 @@ Dorsal, lateral, and ventral views of Fig. 3. Dorsal view of head of holotype of - + Neblinichthys peniculatus , MBUCV diff --git a/data/73/72/87/737287D7FFBEEC29FDB0FE24FB35F81A.xml b/data/73/72/87/737287D7FFBEEC29FDB0FE24FB35F81A.xml new file mode 100644 index 00000000000..4b88eca9e18 --- /dev/null +++ b/data/73/72/87/737287D7FFBEEC29FDB0FE24FB35F81A.xml @@ -0,0 +1,495 @@ + + + +Flourishing in subterranean ecosystems: Euro-Mediterranean Plusiocampinae and tachycampoids (Diplura, Campodeidae) + + + +Author + +Sendra, Alberto +A39300D8-0D4F-426D-8138-FE72D5700B83 +Research Team on Soil Biology and Subterranean Ecosystems, Department of Life Sciences, Faculty of Biology, Chemistry and Environmental Sciences, University of Alcalá (UAH), A. P. 20, Campus Universitario, 28805 Alcalá de Henares, Madrid, Spain. & Colecciones Entomológicas Torres-Sala, Servei de Patrimoni Històric, Ajuntament de València, 46230 València, Spain. +alberto.sendra@uv.es + + + +Author + +Antić, Dragan +A3774DC0-0710-4F91-8F36-F18620D694E0 +University of Belgrade, Faculty of Biology, Institute of Zoology, Studentski trg 16, 11000 Belgrade, Serbia. +dragan.antic@bio.bg.ac.rs + + + +Author + +Barranco, Pablo +060BC3CC-A1A7-4BC2-A408-22077A125EED +Department of Biology and Geology, University of Almería, 04120 Almería, Spain. +Pablo.Barranco@ual.es + + + +Author + +Borko, Špela +743B3331-4D63-4FB4-A5A1-5E876445E6F6 +SubBio Lab, Department of Biology, Biotechnical Faculty, University of Ljubljana, Večna pot 111, 1000 Ljubljana, Slovenia. +borko.spela@gmail.com + + + +Author + +Christian, Erhard +AD4A7348-B28F-44AD-BDA0-FB04E969F5B9 +Institute of Zoology, University of Natural Resources and Life Sciences, Gregor Mendel Str. 33, 1180 Vienna, Austria. +erhard.christian@boku.ac.at + + + +Author + +Delić, Teo +D38183EA-6034-4634-8DD1-45FF9C73D2B4 +SubBio Lab, Department of Biology, Biotechnical Faculty, University of Ljubljana, Večna pot 111, 1000 Ljubljana, Slovenia. +Teo.Delic@bf.uni-lj.si + + + +Author + +Fadrique, Floren +90C2A5C4-A7ED-4DCA-8207-4692B7B81078 +Associació Catalana de Biospeleologia (BIOSP), C / Moreres 3, lʼHospitalet de lʼInfant, 43890 Tarragona, Spain. +ffadrique@hotmail.com + + + +Author + +Faille, Arnaud +34F015D0-0840-478A-BFE2-AA2B1F6D05D5 +Stuttgart State Museum of Natural History, Rosenstein 1, 70191 Stuttgart, Germany. +arnaud.faille@mnhn.fr + + + +Author + +Galli, Loris +976A4615-5713-461B-B48B-7658D7125276 +Department of Earth, Environment and Life Sciences, University of Genova, Corso Europa 26, 16132 Genova, Italy. +loris.galli@unige.it + + + +Author + +Gasparo, Fulvio +F65C1400-2AEA-42BE-8886-0A4B6C6789B0 +Commissione Grotte “ E. Boegan ”, Società Alpina delle Giulie, C. A. I., Via Donota 2, 34121 Trieste, Italy. +fulvio.gasparo@libero.it + + + +Author + +Georgiev, Dilian +B9816B63-8496-4EA6-81C0-4DB62EA331DA +Department of Ecology and Environmental Conservation, University of Plovdiv, Tzar Assen Str. 24, 4000 Plovdiv, Bulgaria. +diliangeorgiev@abv.bg + + + +Author + +Giachino, Pier Mauro +3EB353B6-3A14-4906-9805-BDD79D457E71 +Settore Fitosanitario Regionale, Environment Park, Palazzina A 2, via Livorno 60, 10144 Torino, Italy. & Department of Zoology, Institute of Biology and Ecology, Faculty of Science, P. J. Šafárik University, Šrobárova 2, 04180 Košice, Slovakia. +PierMauro.Giachino@regione.piemonte.it + + + +Author + +Kovac, L'ubomír +64C6117E-DB5C-4569-BF89-5C812C118760 +Department of Zoology, Institute of Biology and Ecology, Faculty of Science, P. J. Šafárik University, Šrobárova 2, 04180 Košice, Slovakia. +lubomir.kovac@upjs.sk + + + +Author + +Lukić, Marko +6B455B4B-F0E4-4545-99C0-1CC87BD81327 +Croatian Biospeleological Society, Demetrova 1, 10000 Zagreb, Croatia. +marko.lukic@hbsd.hr + + + +Author + +Marcia, Paolo +505E7088-28A6-46BA-88BD-9343C99BC36E +Department of Veterinary Medicine, University of Sassari, 07100 Sassari, Sardinia, Italy. +pmarcia@uniss.it + + + +Author + +Miculinić, Kazimir +DD0FC3F4-8D9C-481E-B292-BB180DD1CA20 +Croatian Biospeleological Society, Demetrova 1, 10000 Zagreb, Croatia. +miculinic@yahoo.com + + + +Author + +Nicolosi, Giuseppe +FEF08BB9-468B-4C02-A757-84B5EDDA6BAA +Department of Life Sciences and Systems Biology, University of Turin, Via Accademia Albertina 13, 10123 Torino, Italy. +gnicolosi@hotmail.it + + + +Author + +Palero, Ferran +6FDDFE46-501A-4D6E-975E-72F55617775C +Department of Invertebrate Zoology and Hydrobiology, Faculty of Biology and Environmental Protection, University of Łódź, ul. Banacha 12 / 16, 90 - 237 Łódź, Poland. & Department of Life Sciences, The Natural History Museum, Cromwell Road, London SW 7 5 BD, UK. +fpalero@gmail.com + + + +Author + +Paragamian, Kaloust +10B3AD4F-1AF6-4111-80B8-043D4EE675EE +Hellenic Institute of Speleological Research, Ethnikis Antistaseos 82, 71306 Irakleion, Crete, Greece +k.paragamian@wwf.gr + + + +Author + +Pérez, Toni +9CB76198-1B76-4D5B-9578-5EF6F1B68E51 +Grupo de Espeleología de Villacarrillo, Plaza 28 de Febrero, nº 5, 1 º – 2 ª, 23300 Villacarrillo (Jaén), Spain +bioespeleologiaGEV@gmail.com + + + +Author + +Polak, Slavko +1E119F76-B3F0-4E37-BB3F-9216AFB5CD88 +Notranjska Museum Postojna, Kolodvorska c. 3, 6230 Postojna, Slovenia. +slavko.polak@guest.arnes.si + + + +Author + +Prieto, Carlos E. +CAC20D21-78FF-4B8A-8023-F06A06EA031F +Departamento de Zoología y Biología Celular Animal, University of the Basque Country, P. O. Box 644, 48080 Bilbao, Spain. +ggpprsic@lg.ehu.es + + + +Author + +Turbanov, Ilya +E8F01940-9A2B-4153-9106-A6AF2A79D0A1 +Institute of the Biology of Inland Waters, Russian Academy of Sciences, Borok, Yaroslavl Region, 1527432 Russia & Cherepovets State University, Cherepovets, Vologda Region, 162600 Russia +turba13@mail.ru + + + +Author + +Vailati, Dante +6D052C67-2975-4BD1-B7F2-B537F21FE625 +Via Interna 8, 25127 Brescia, Italy +dante.vailati@libero.it + + + +Author + +Reboleira, Ana Sofia P. S. +338DE845-4839-4EF5-B684-587C021F076C +Natural History Museum of Denmark, University of Copenhagen, Universitetsparken 15, 2100 Copenhagen Ø, Denmark +sreboleira@snm.ku.dk + +text + + +European Journal of Taxonomy + + +2020 + +2020-01-10 + + +591 + + +1 +138 + + + +journal article +10.5852/ejt.2020.591 +61d609de-bcb3-4490-ac65-ba7cacda2d72 +2118-9773 +3659823 +5CB610DA-F9C9-4213-80E8-8A8901895A18 + + + + +Subfamily + +Plusiocampinae +Paclt, 1957 + + + + + + +Plusiocampinae +Paclt, 1957: 42 + +. + + + + +Diagnosis +( +Condé 1955a +; +Paclt 1957 +; + +Sendra +et al. +2017a + +) + + +Since the only diagnostic character of +Plusiocampinae +(as suggested by +Paclt 1957 +) is the higher number of macrosetae on the pronotum, this taxon seems to be paraphyletic. The pronotum never has less than 4+4 macrosetae. However, many of the genera can be considered monophyletic within +Plusiocampinae +. This is the case for + +Anisuracampa + +, + +Cestocampa + +, + +Condeicampa + +, + +Hystrichocampa + +, + +Patrizicampa + +, + +Plusiocampa + +, + +Plutocampa + +, + +Simlacampa + +and + +Vandelicampa + +, characterized by pretarsal lateral crests. Nonetheless, these lateral crests are absent in + +Silvestricampa + +and + +Turkmenocampa + +, clearly isolating them from the other genera. + + + + + + +Key to the genera of +Plusiocampinae + + + +1. Pretarsal claws with lateral crests....................................................................................................2 +– Pretarsal claws without lateral crests...............................................................................................7 +2. Pretarsal lateral processes setiform...................................................................................................3 +– Pretarsal lateral processes laminar barbed or absent.......................................................................5 + +3. Pretarsal lateral processes pubescent ................................................. + +Hystrichocampa +Condé, 1948 + + +– Pretarsal lateral process smooth.......................................................................................................4 + +4. 4+4 macrosetae on urosternites II–VII, 1+1 macrosetae on urosternite VIII ..................................... .............. + +Condeicampa +Ferguson, 1996 + +and + + +Plusiocampa +( +Dydimocampa +) +sinensis + +Silvestri, 1931 + + + +– No less than 5+5 macrosetae on urosternites II–VII and 2+2 macrosetae on urosternite VIII ........ ................................................................................................................ + +Plusiocampa +Silvestri, 1912 + + + +5. Pretarsal lateral processes absent ........................................................ + +Plutocampa +Chevrizov, 1978 + + +– Pretarsal lateral processes laminar barbed.......................................................................................6 + +6. Pretarsal lateral processes laminar ......................................................... + +Cestocampa +Condé, 1955 + +, + +Vandelicampa +Condé, 1955 + +, + +Patrizicampa +Condé, 1956 + +, + +Anisuracampa +Xie & Yang, 1991 + +, + + +Plusiocampa +( +Didymocampa +) +lipsae + +Condé, 1993 + +and + +Plusiocampa kashiensis +(Chou & Tong, 1980) + + + +– Pretarsal lateral processes narrow ............................................................ + +Simlacampa +Condé, 1956 + + + +7. Simple claws; pretarsal lateral processes absent, medial-intermediate and lateral-intermediate macrosetae on mesonotum and metanotum ........................................... + +Silvestricampa +Condé, 1950 + + + +– Pretarsal claws with sharp side-shoot; pretarsal lateral processes laminar, without medial posterior macrosetae on mesonotum and metanotum ........................ + +Turkmenocampa +Sendra & Stoev, 2017 + + + + + +This key includes 11 accepted genera plus three species, + +Plusiocampa +( +Dydimocampa +) +sinensis + +, + +Plusiocampa +( +Dydimocampa +) +lipsae + +and + +Plusiocampa kashiensis + +from +China +, which remain in an uncertain position ( + +Sendra +et al. +2012a + +). Three new troglomorphic genera from +China +, Indochina and the Aegean islands, which are currently under description (Sendra, in prep.), are excluded. + + + + \ No newline at end of file