diff --git a/data/03/9B/49/039B4953FFB44806793AFD81FAD44903.xml b/data/03/9B/49/039B4953FFB44806793AFD81FAD44903.xml index 64d0451de13..f7c1863c970 100644 --- a/data/03/9B/49/039B4953FFB44806793AFD81FAD44903.xml +++ b/data/03/9B/49/039B4953FFB44806793AFD81FAD44903.xml @@ -1,66 +1,66 @@ - - - -Revision of the Eurasian species of Aegilips Haliday, 1835 (Hymenoptera: Figitidae: Anacharitinae) + + + +Revision of the Eurasian species of Aegilips Haliday, 1835 (Hymenoptera: Figitidae: Anacharitinae) - - -Author + + +Author -Mata-Casanova, Noel -41ABC9C0-AB40-4D75-AB30-0CFC62704A05 -Universitat de Barcelona, Facultat de Biologia, Departament de Biologia Evolutiva, Ecologia i Ciències Ambientals. Avda. Diagonal 645, 08028 - Barcelona, Spain. -feofitotu@gmail.com +Mata-Casanova, Noel +41ABC9C0-AB40-4D75-AB30-0CFC62704A05 +Universitat de Barcelona, Facultat de Biologia, Departament de Biologia Evolutiva, Ecologia i Ciències Ambientals. Avda. Diagonal 645, 08028 - Barcelona, Spain. +feofitotu@gmail.com - - -Author + + +Author -Selfa, Jesús -C01B4FA6-6C5C-4DDF-A114-2B06D8FE4D20 -Universitat de València, Facultat de Ciències Biològiques, Departament de Zoologia. Campus de Burjassot-Paterna, Dr. Moliner 50, E- 46100 Burjassot (València), Spain. -jesus.selfa@uv.es +Selfa, Jesús +C01B4FA6-6C5C-4DDF-A114-2B06D8FE4D20 +Universitat de València, Facultat de Ciències Biològiques, Departament de Zoologia. Campus de Burjassot-Paterna, Dr. Moliner 50, E- 46100 Burjassot (València), Spain. +jesus.selfa@uv.es - - -Author + + +Author -Pujade-Villar, Juli -94C497E0-C6A1-48BD-819D-FE5A8036BECD -Universitat de Barcelona, Facultat de Biologia, Departament de Biologia Evolutiva, Ecologia i Ciències Ambientals. Avda. Diagonal 645, 08028 - Barcelona, Spain. -jpujade@ub.edu +Pujade-Villar, Juli +94C497E0-C6A1-48BD-819D-FE5A8036BECD +Universitat de Barcelona, Facultat de Biologia, Departament de Biologia Evolutiva, Ecologia i Ciències Ambientals. Avda. Diagonal 645, 08028 - Barcelona, Spain. +jpujade@ub.edu -text - - -European Journal of Taxonomy +text + + +European Journal of Taxonomy - -2022 - -2022-05-16 + +2022 + +2022-05-16 - -819 + +819 - -108 -139 + +108 +139 - -http://zoobank.org/e4555fef-00d2-40da-8ce5-459c6181b68c + +http://zoobank.org/e4555fef-00d2-40da-8ce5-459c6181b68c -journal article -55467 -10.5852/ejt.2022.819.1781 -5828a31f-669c-4994-904e-0e16f9ae07ed -2118-9773 -6564565 -E4555FEF-00D2-40DA-8CE5-459C6181B68C +journal article +55467 +10.5852/ejt.2022.819.1781 +5828a31f-669c-4994-904e-0e16f9ae07ed +2118-9773 +6564565 +E4555FEF-00D2-40DA-8CE5-459C6181B68C - + @@ -93,19 +93,20 @@ - + Anacharis flavidicornis Kieffer, 1911: 121 -. Replacement name for +. + +Replacement name for Anacharis flavicornis . - diff --git a/data/03/B0/87/03B087DCFFF68B2F5E8FFB352616F84B.xml b/data/03/B0/87/03B087DCFFF68B2F5E8FFB352616F84B.xml index 89fe8ab953c..1fbe9832463 100644 --- a/data/03/B0/87/03B087DCFFF68B2F5E8FFB352616F84B.xml +++ b/data/03/B0/87/03B087DCFFF68B2F5E8FFB352616F84B.xml @@ -1,82 +1,82 @@ - - - -Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants + + + +Ebenacobius Haran, a new southern African genus of flower weevils (Coleoptera: Curculioninae: Derelomini) associated with dicotyledonous plants - - -Author + + +Author -Haran, Julien -A04E1722-994A-44AD-8FD2-28DC0F220805 -CBGP, CIRAD, Montpellier SupAgro, INRAe, IRD, Montpellier University, Montpellier, France. -julien.haran@cirad.fr +Haran, Julien +A04E1722-994A-44AD-8FD2-28DC0F220805 +CBGP, CIRAD, Montpellier SupAgro, INRAe, IRD, Montpellier University, Montpellier, France. +julien.haran@cirad.fr - - -Author + + +Author -Benoit, Laure -61963F74-724B-4174-9E9A-8817A3516B0E -CBGP, CIRAD, Montpellier SupAgro, INRAe, IRD, Montpellier University, Montpellier, France. -Laure.Benoit@cirad.fr +Benoit, Laure +61963F74-724B-4174-9E9A-8817A3516B0E +CBGP, CIRAD, Montpellier SupAgro, INRAe, IRD, Montpellier University, Montpellier, France. +Laure.Benoit@cirad.fr - - -Author + + +Author -Procheş, Şerban -0ACCE987-9774-453B-A1BA-42E93D75D3C7 -Centre for Functional Biodiversity and Discipline of Geography, University of KwaZulu-Natal, Durban, South Africa. 4 CBGP, INRAE, CIRAD, IRD, Institut Agro, Univ Montpellier, Montpellier, France. -setapion@gmail.com +Procheş, Şerban +0ACCE987-9774-453B-A1BA-42E93D75D3C7 +Centre for Functional Biodiversity and Discipline of Geography, University of KwaZulu-Natal, Durban, South Africa. +setapion@gmail.com - - -Author + + +Author -Kergoat, Gael J. -D763F7EC-A1C9-45FF-88FB-408E3953F9A8 -gael.kergoat@inrae.fr +Kergoat, Gael J. +D763F7EC-A1C9-45FF-88FB-408E3953F9A8 +CBGP, INRAE, CIRAD, IRD, Institut Agro, Univ Montpellier, Montpellier, France. +gael.kergoat@inrae.fr -text - - -European Journal of Taxonomy +text + + +European Journal of Taxonomy - -2022 - -2022-05-05 + +2022 + +2022-05-05 - -818 + +818 - -1 + +1 - -1 -54 + +1 +54 - -http://dx.doi.org/10.5852/ejt.2022.818.1771 + +http://dx.doi.org/10.5852/ejt.2022.818.1771 -journal article -55593 -10.5852/ejt.2022.818.1771 -c6f4d05a-7619-4e78-9d1f-f5becd279615 -2118-9773 -6532969 -17950060-6B62-4479-BAF0-473767DC6ADB +journal article +10.5852/ejt.2022.818.1771 +c6f4d05a-7619-4e78-9d1f-f5becd279615 +2118-9773 +6532969 +17950060-6B62-4479-BAF0-473767DC6ADB - + Key to genera of afrotropical continental -Derelomini +Derelomini (sensu Franz 2006 ) diff --git a/data/03/B7/BE/03B7BE366756FFCBFD9CF9D0FE026AB4.xml b/data/03/B7/BE/03B7BE366756FFCBFD9CF9D0FE026AB4.xml index 165b295163f..71d7b4725a5 100644 --- a/data/03/B7/BE/03B7BE366756FFCBFD9CF9D0FE026AB4.xml +++ b/data/03/B7/BE/03B7BE366756FFCBFD9CF9D0FE026AB4.xml @@ -1,60 +1,59 @@ - - - -Cheilosia (Diptera, Syrphidae: Rhingiini) of Nepal with descriptions of 29 new species + + + +Cheilosia (Diptera, Syrphidae: Rhingiini) of Nepal with descriptions of 29 new species - - -Author + + +Author -Barkalov, Anatolij V. -F79ADCEA-0136-46E9-8D20-F0A7CCA238CF -Institute of Systematics and Ecology of Animals, Russian Academy of Sciences, Siberian Branch, 11 Frunze str., 630091 Novosibirsk, Russia. -bark@eco.nsc.ru +Barkalov, Anatolij V. +F79ADCEA-0136-46E9-8D20-F0A7CCA238CF +Institute of Systematics and Ecology of Animals, Russian Academy of Sciences, Siberian Branch, 11 Frunze str., 630091 Novosibirsk, Russia. +bark@eco.nsc.ru - - -Author + + +Author -Ståhls, Gunilla -D19B1262-503A-48E2-91AE-F99D0F2EA3A3 -Zoology Unit, Finnish Museum of Natural History Luomus, PO Box 17, 00014 University of Helsinki, Finland. -gunilla.stahls@helsinki.fi +Ståhls, Gunilla +D19B1262-503A-48E2-91AE-F99D0F2EA3A3 +Zoology Unit, Finnish Museum of Natural History Luomus, PO Box 17, 00014 University of Helsinki, Finland. +gunilla.stahls@helsinki.fi -text - - -European Journal of Taxonomy +text + + +European Journal of Taxonomy - -2022 - -2022-07-14 + +2022 + +2022-07-14 - -829 + +829 - -1 + +1 - -1 -127 + +1 +127 - -http://dx.doi.org/10.5852/ejt.2022.829.1863 + +http://dx.doi.org/10.5852/ejt.2022.829.1863 -journal article -99300 -10.5852/ejt.2022.829.1863 -a760e4b7-93a7-47c0-b887-035504d88bd6 -2118-9773 -6839936 -DF4FB22A-133C-4826-BAC2-896CA2CB483D +journal article +10.5852/ejt.2022.829.1863 +a760e4b7-93a7-47c0-b887-035504d88bd6 +2118-9773 +6839936 +DF4FB22A-133C-4826-BAC2-896CA2CB483D - + @@ -74,7 +73,7 @@ Barkalov & Peck, 1997 - + Cheilosia erratica Barkalov & Peck, 1997a: 1173 @@ -118,7 +117,7 @@ Barkalov & Peck, 1997 -Cheilosia erratica +Cheilosia erratica – diff --git a/data/03/B7/BE/03B7BE366775FFEEFF01FE1EFA9568D7.xml b/data/03/B7/BE/03B7BE366775FFEEFF01FE1EFA9568D7.xml index cedd74743ad..cf76725241e 100644 --- a/data/03/B7/BE/03B7BE366775FFEEFF01FE1EFA9568D7.xml +++ b/data/03/B7/BE/03B7BE366775FFEEFF01FE1EFA9568D7.xml @@ -1,58 +1,57 @@ - - - -Cheilosia (Diptera, Syrphidae: Rhingiini) of Nepal with descriptions of 29 new species + + + +Cheilosia (Diptera, Syrphidae: Rhingiini) of Nepal with descriptions of 29 new species - - -Author + + +Author -Barkalov, Anatolij V. -F79ADCEA-0136-46E9-8D20-F0A7CCA238CF -Institute of Systematics and Ecology of Animals, Russian Academy of Sciences, Siberian Branch, 11 Frunze str., 630091 Novosibirsk, Russia. -bark@eco.nsc.ru +Barkalov, Anatolij V. +F79ADCEA-0136-46E9-8D20-F0A7CCA238CF +Institute of Systematics and Ecology of Animals, Russian Academy of Sciences, Siberian Branch, 11 Frunze str., 630091 Novosibirsk, Russia. +bark@eco.nsc.ru - - -Author + + +Author -Ståhls, Gunilla -D19B1262-503A-48E2-91AE-F99D0F2EA3A3 -Zoology Unit, Finnish Museum of Natural History Luomus, PO Box 17, 00014 University of Helsinki, Finland. -gunilla.stahls@helsinki.fi +Ståhls, Gunilla +D19B1262-503A-48E2-91AE-F99D0F2EA3A3 +Zoology Unit, Finnish Museum of Natural History Luomus, PO Box 17, 00014 University of Helsinki, Finland. +gunilla.stahls@helsinki.fi -text - - -European Journal of Taxonomy +text + + +European Journal of Taxonomy - -2022 - -2022-07-14 + +2022 + +2022-07-14 - -829 + +829 - -1 + +1 - -1 -127 + +1 +127 - -http://dx.doi.org/10.5852/ejt.2022.829.1863 + +http://dx.doi.org/10.5852/ejt.2022.829.1863 -journal article -99300 -10.5852/ejt.2022.829.1863 -a760e4b7-93a7-47c0-b887-035504d88bd6 -2118-9773 -6839936 -DF4FB22A-133C-4826-BAC2-896CA2CB483D +journal article +10.5852/ejt.2022.829.1863 +a760e4b7-93a7-47c0-b887-035504d88bd6 +2118-9773 +6839936 +DF4FB22A-133C-4826-BAC2-896CA2CB483D @@ -60,7 +59,7 @@ Key to subgenera of - + Cheilosia occurring in diff --git a/data/03/C4/C5/03C4C50EFFE0B12DFEDC1F63CBDBBD54.xml b/data/03/C4/C5/03C4C50EFFE0B12DFEDC1F63CBDBBD54.xml new file mode 100644 index 00000000000..f18c801f8e2 --- /dev/null +++ b/data/03/C4/C5/03C4C50EFFE0B12DFEDC1F63CBDBBD54.xml @@ -0,0 +1,205 @@ + + + +Unravelling the obscure homology: postembryonic development of chaetotaxic traits in a basal hexapod taxon (Collembola: Tomoceridae) + + + +Author + +Yu, Daoyuan + + + +Author + +Zhang, Yating + + + +Author + +Wang, Ziqiang + + + +Author + +Hu, Feng + + + +Author + +Liu, Manqiang + +text + + +Zoological Journal of the Linnean Society + + +2024 + +2024-02-19 + + +202 + + +3 + + +1 +20 + + + + +https://doi.org/10.1093/zoolinnean/zlae020 + +journal article +10.1093/zoolinnean/zlae020 +0024-4082 +14276780 + + + + + + +Tomocerus nan + + + + + + +Specimens examined. 15HN2TJ (1–5), +25.xii.2015 +, leg. Daoyuan Yu and Chunyan Qin. + + + + +Head: +First instar ( +Fig. 8A +). The pattern is identical to that of + +T. tropicus + +. + + +Third instar ( +Fig. 8B +). Chaetal transformation similar to that of + +T. nabanensis + +at the third instar, but S0 and Pp3 become microchaetae. Secondary chaetae An1a, An1p, An3a, An3a2, An3a3, Pa5a, Pp1i, and Pp3e appear. + + +Adult macrochaetotaxy ( +Fig. 10C +). The pattern is very similar to that of + +T. nabanensis + +, but S0 is a microchaeta. + + +Th. II: +First instar ( +Fig. 9A +). The patterns of ordinary chaetae, s-microchaetae, and pseudopores are very similar to those of + +T. tropicus + +, except that a2 is a mesochaeta. Six normal s-chaetae are present on the lateral side. + + +Third instar ( +Fig. 9B +). Primary mesochaeta p3 becomes a macrochaeta; a6 and m6 become bothriotricha; macrochaetae a5 and ap5, and mesochaetae except for a7, m7, and p6 become microchaetae. Chaetal movement and neochaetosis of macro- and mesochaetae are very similar to those of + +T. tropicus + +. About 15 microchaetae appear in a scattered manner. The pattern of s-chaetae remains unchanged. + + +Adult macrochaetotaxy ( +Fig. 11C +). Besides the collar and aa’ series, chaetae a3, a4, m3, and p2–4 are macrochaetae; a6 and m6 are bothriotricha. + + +Th. III, Abd. I, Abd. II, and Abd. III: +The primary patterns ( +Fig. 9A +), postembryonic changes ( +Fig. 9B +), and final patterns are almost identical to those of + +T. tropicus + +, except for minor differences in chaetal positions and fewer microchaetae. + + +Abd. IV: +First instar ( +Fig. 9A +). The patterns of ordinary chaetae, bothriotricha, and pseudopores are similar to those of + +T. tropicus + +, but +pm7 and ap2 are absent, and p7 is a mesochaeta. About +14–17 normal and 11–14 long s-chaetae are present. The five +most posterior long s-chaetae are the longest (shorter than Abd. V), and are each associated with a mesochaeta in row p (p1–5). The other long s-chaetae are subequal in length. + + +Third instar ( +Fig. 9B +). Primary chaeta p7 becomes a macrochaeta. Other changes are almost identical to those in + +T. tropicus + +. + + +Adult macrochaetotaxy. The pattern is identical to that of + +T. tropicus + +. + + +Abd. V: +The primary pattern ( +Fig. 9A +), postembryonic changes ( +Fig. 9B +), and final pattern are almost identical to those of + +T. nabanensis + +, except that some mesochaetae become microchaetae in different instars. + + +Abd. VI: +The primary chaetotaxy ( +Fig. 9A +) is identical to that of + +T. tropicus + +. + +Status in the later instars and adult is not observed. +S-chaetotaxy from Th. II to Abd. V +Normal s-chaetae: 6/6/5/5/5/14–17 * 11–14 (long)/6 +S-microchaetae: 1/1/0/0/1/0/0. + + + \ No newline at end of file diff --git a/data/03/C4/C5/03C4C50EFFE3B12DFEEE1B31CEA4BD6B.xml b/data/03/C4/C5/03C4C50EFFE3B12DFEEE1B31CEA4BD6B.xml new file mode 100644 index 00000000000..82a70c2bebf --- /dev/null +++ b/data/03/C4/C5/03C4C50EFFE3B12DFEEE1B31CEA4BD6B.xml @@ -0,0 +1,302 @@ + + + +Unravelling the obscure homology: postembryonic development of chaetotaxic traits in a basal hexapod taxon (Collembola: Tomoceridae) + + + +Author + +Yu, Daoyuan + + + +Author + +Zhang, Yating + + + +Author + +Wang, Ziqiang + + + +Author + +Hu, Feng + + + +Author + +Liu, Manqiang + +text + + +Zoological Journal of the Linnean Society + + +2024 + +2024-02-19 + + +202 + + +3 + + +1 +20 + + + + +https://doi.org/10.1093/zoolinnean/zlae020 + +journal article +10.1093/zoolinnean/zlae020 +0024-4082 +14276780 + + + + + + +Tomocerus nabanensis + + + + + + +Specimens examined. 17BN1TJ (1–8), +vii.2017 +, leg. Shengjie Liu. + + + + +Head: +First instar ( +Fig. 5A +). The pattern is identical to that of + +T. tropicus + +. + + +Second instar ( +Fig. 5B +). The chaetal transformation is identical to that of + +T. tropicus + +. The neochaetosis is also similar, with the exception that the secondary chaeta An1a appears instead of An1a0 and A2a0. + + +Third instar ( +Fig. 5C +). Macrochaetae Pm1, Pp1, and Pe2 become mesochaetae. Pp3 becomes distinctly smaller. Secondary chaetae An1p, An3a2, An3i, A2a0, and Pe3i appear. + + +Fourth instar ( +Fig. 5D +). Pm1, Pp1, Pp3, and Pe2 become microchaetae. Additional micro- and mesochaetae appear only in row An and along the postoccipital collar. + + +Adult macrochaetotaxy ( +Fig. 10B +). The pattern is very similar to that of + +T. tropicus + +, but Pp3 is a microchaeta. + + +Th. II: +First instar ( +Fig. 6A +). The patterns of ordinary chaetae, s-microchaetae, and pseudopores are identical to that of + +T. tropicus + +. About 10–13 normal s-chaetae are present. + + +Second instar ( +Fig. 6B +). Primary chaetae m1, m2, and p3 become macrochaetae; m6 becomes a bothriotrichum; ap5 becomes a mesochaeta; m4, am5, and p1 become microchaetae. Chaetal movement and neochaetosis of macro- and mesochaetae are similar to those of + +T. tropicus + +, but a4 is devoid of associated secondary chaetae at this stage. About 10 microchaetae appear in a scattered manner. The number of s-chaetae remains unchanged. + + +Third instar ( +Fig. 7A +). The changes are very similar to those in + +T. tropicus + +, except that about five additional microchaetae appear. + + +Fourth instar ( +Fig. 7B +). The changes are very similar to those in + +T. tropicus + +, including the transformation of a6 into a bothriotrichum. + + +Adult macrochaetotaxy ( +Fig. 11B +). Collar and aa’ series of macrochaetae are well developed. Chaetae a2–5, m1–3, and p2–4 are macrochaetae; a6 and m6 are bothriotricha. + + +Th. III, Abd. I, and II: +The first instar ( +Fig. 6A +), postembryonic development ( +Figs 6B +, +7 +), and adult macrochaetotaxy are almost identical to those of + +T. tropicus + +, except for minor differences in the transformation and addition of microchaetae. + + +Abd. III: +First instar ( +Fig. 6A +). The pattern is almost identical to that of + +T. tropicus + +, with minor difference in some chaetal positions. + + +Postembryonic development ( +Figs 6B +, +7 +). The changes are very similar to those in + +T. tropicus + +, except that the transformation of p6 and addition of microchaetae occur later. + + +Adult macrochaetotaxy. The pattern is identical to that of + +T. tropicus + +. + + +Abd. IV: +First instar ( +Fig. 6A +). The patterns of ordinary chaetae, bothriotricha, and pseudopores are identical to those of + +T. tropicus + +. A total of 21–25 normal and 12–13 long s-chaetae are present. The five most posterior long s-chaetae are the longest (subequal to the length of Abd. +V +), and are each associated with a mesochaeta in row p (p1–5). The other long s-chaetae are subequal in length. + + +Postembryonic development ( +Figs 6B +, +7 +). The changes are very similar to those in + +T. tropicus + +, except for minor and apparently random differences in microchaetae and lateral mesochaetae. + + + +Figure 5. +Cephalic chaetotaxy of + +Tomocerus nabanensis + +. A, First instar; (B) second instar; (C) third instar; (D) fourth instar. + + + + +Figure 6. +Tergal chaetotaxy of + +Tomocerus nabanensis + +. A, First instar; (B) second instar. + + + +Adult macrochaetotaxy. The pattern is identical to that of T. + +tropicus + +. + + +Abd. V: +First instar ( +Fig. 6A +). The pattern of ordinary chaetae is almost identical to that of + +T. tropicus + +, except that in one case p4 is absent. Six normal s-chaetae are present, with two in front of row a, two between row a and m, one posterior to p6, and one beside el. Occasionally, the s-chaeta posterior to a3 is absent and +an extra +s-chaeta is present posterior to p6. + + +Postembryonic development ( +Figs 6B +, +7 +). The changes are almost identical to those in + +T. tropicus + +, except that some mesochaetae become microchaetae in different instars. + + +Adult macrochaetotaxy. The pattern is identical to that of + +T. tropicus + +. + + +Abd. VI: +The chaetotaxy at the first two instars ( +Fig. 6 +) is identical to that of + +T. tropicus + +. + +Status in the later instars and adult is not observed. +S-chaetotaxy from Th. II to Abd. V +Normal s-chaetae: 10–13/6/5/5/5/21–25 * 12–13 (long)/6 +S-microchaetae: 1/1/0/0/1/0/0. + + + \ No newline at end of file diff --git a/data/03/C4/C5/03C4C50EFFE9B12EFB911A55CEB5B89F.xml b/data/03/C4/C5/03C4C50EFFE9B12EFB911A55CEB5B89F.xml new file mode 100644 index 00000000000..a48eb9a7dc8 --- /dev/null +++ b/data/03/C4/C5/03C4C50EFFE9B12EFB911A55CEB5B89F.xml @@ -0,0 +1,384 @@ + + + +Unravelling the obscure homology: postembryonic development of chaetotaxic traits in a basal hexapod taxon (Collembola: Tomoceridae) + + + +Author + +Yu, Daoyuan + + + +Author + +Zhang, Yating + + + +Author + +Wang, Ziqiang + + + +Author + +Hu, Feng + + + +Author + +Liu, Manqiang + +text + + +Zoological Journal of the Linnean Society + + +2024 + +2024-02-19 + + +202 + + +3 + + +1 +20 + + + + +https://doi.org/10.1093/zoolinnean/zlae020 + +journal article +10.1093/zoolinnean/zlae020 +0024-4082 +14276780 + + + + + +Tomocerus tropicus + + + + + +Specimens examined. 15HN5TCJ (1–11), +29.xii.2015 +, leg. Daoyuan Yu and Chunyan Qin. Cultured in the lab. + + + + +Head: +First instar ( +Fig. 2A +). Numbers of chaetae in each row are as follows. An: 2; A: 4; M: 5; S: 5; ocular: 3; Ps: 3; Pi: 1; Pa: 4; Pm: 3; Pp: 2; Pe: 2. Chaetae Pa2, Pa5, Pp1, Pp3, and Pe2 are macrochaetae, others are mesochaetae. + + +Second instar ( +Fig. 2B +). Primary chaetae A2, A3, A5, M2, S0, S2, S5, S6, Pa6, and Pm1 turn into macrochaetae; most mesochaetae turn into microchaetae except for the row An, Pe, and M4. Secondary mesochaetae An3a, Pe2i, and Pe2e, and microchaeta Pa5a and Pp3e appear constantly, whereas mesochaeta An1a0 and microchaeta A2a0 in the middle line are either present or absent. + + + +Figure 1. +Chaetal types on the head and terga in + +Tomocerus + +. A, Chaetae drawn under an optical microscope, showing graphic symbols used in the following figures; (B–G) scanning electron microscopic photos of a microchaeta (B), a strongly serrated macrochaeta (C), a bothriotrichum (D), an s-chaeta (E), an s-microchaeta (F), and a scale (G). + + + +Third instar ( +Fig. 2C +). Pm1, Pp1, and Pe2 become distinctly smaller (relative size), but still retain the morphology of macrochaetae. Secondary microchaetae An1p and An3a2 are present. + + +Fourth instar ( +Fig. 2D +). The relative sizes of macrochaetae Pm1, Pp1, and Pe2 reduce further. Additional micro- and mesochaetae appear only in row An and along the postoccipital collar. + + +Adult macrochaetotaxy ( +Fig. 10A +). A2, A3, A5, M2, S0, S2, S5, S6, Pa2, Pa5, Pa6, and Pp3 are macrochaetae. Antennal base and postoccipital collar each with a row of chaetae. Other chaetae are all microchaetae, and are often obscured by dense scales. + + + +Figure 2. +Cephalic chaetotaxy of + +Tomocerus tropicus + +. A, First instar; (B) second instar; (C) third instar; (D) fourth instar. + + + + +Th. II: +First instar (Fig. 3A). Numbers of chaetae in each + +row are as follows. Row a: 6; row m: 7 * 1 (outlier); row p: 6 * 1. Chaetae a2–6, m3, m6, p2, p4, and ap5 are macrochaetae, others are mesochaetae. One s-microchaeta and 12–16 normal s-chaetae are present on the lateral side. The s-microchaeta is between a6 and m7. The pseudopore is near m2. +An extra +macrochaeta is present near p +5 in +only +one specimen +. + + +Second instar ( +Fig. 3B +). Primary chaetae m4 and p3 become macrochaetae; m6 becomes a bothriotrichum; ap5 becomes a mesochaeta; m1, m2, m5, am5, and p1 become microchaetae. Chaetae in the antero-lateral corner (a6, a7, m7, and s-chaetae around them) are moved postero-laterally. Secondary macrochaetae appear anteriorly to row a, forming the collar; secondary mesochaetae appear on the lateral side; about 17 microchaetae appear in a scattered manner. The number of s-chaetae remains unchanged. + + +Third instar ( +Fig. 4A +). The antero-lateral chaetae are moved further postero-laterally. Chaeta p5 becomes a microchaeta. More secondary macrochaetae and mesochaetae appear in the collar. No more microchaeta and s-chaeta appear. Chaeta m4 becomes a mesochaeta (or remains its primary status) in only +one specimen +. + + +Fourth instar ( +Fig. 4B +). Chaeta a6 becomes a bothriotrichum; ap5 becomes a microchaeta. Number of macrochaetae and mesochaetae in the collar increases further. A few microchaetae are added. + + +Adult macrochaetotaxy ( +Fig. 11A +). The anterior margin of the tergum has a medial ‘collar’ formed by the secondary chaetae m.a2a, m.a3a, and m.a4a. Postero-lateral to the collar and anterior to row a are about eight macrochaetae in an approximate row (hereafter called aa’ series), formed by m.a5a, m.a6a, and some members of the m.a4a. Among the primary chaetae, a2–5, m3, m4, and p2–4 are macrochaetae; a6 and m6 are bothriotricha. Patterns of microchaetae and s-chaetae are not determined. + + +Th. III: +First instar ( +Fig. 3A +). Numbers of chaetae in each row are as follows. Row a: 7; row m: 5; row p: 6. Chaetae a4, m6, p1, p3, and p5 are macrochaetae, others are mesochaetae. One s-microchaeta and six normal s-chaetae are present on the lateral side. The s-microchaeta is between a7 and m7. One normal s-chaeta is close to the s-microchaeta, the other five are close to a4, a6, m7, p5, and p6, respectively. The pseudopore is approximately between a1 and m2. + + +Second instar ( +Fig. 3B +). Primary chaetae m6 becomes a bothriotrichum; most mesochaetae become microchaetae except for a7, m7, p2, and p6. Secondary mesochaetae appear on the lateral side; five microchaetae appear near m3, m6, p1, p2, and p5, respectively. The number and position of s-chaetae remain unchanged. + + +Third instar ( +Fig. 4A +). Chaetae p2 and p6 become microchaetae. No other significant changes occur except for the addition of lateral mesochaetae and occasionally a microchaeta beside p1. + + +Fourth instar ( +Fig. 4B +). Chaeta a7 becomes smaller. Other characters remain the same as for the third instar. + + +Adult macrochaetotaxy ( +Fig. 11A +). Chaetae a4, p1, p3, and p5 are macrochaetae; m6 is a bothriotrichum. Patterns of microchaetae and s-chaetae are not determined. + + + +Abd. I: +First instar (Fig. 3A). Numbers of chaetae in each row + +are as follows. Row a: 4; row m: 3; row p: 5. Chaetae m2–4 are macrochaetae, others are mesochaetae. Five normal s-chaetae are present in a posterior row. Four s-chaetae are posterior to m2, m3, m4, and p5, respectively; one s-chaeta is between p5 and p6. The pseudopore is approximately between a1 and m2. + + +Second instar ( +Fig. 3B +). Mesochaetae become microchaetae except for p5 and p6. A secondary mesochaeta appears anteriorly to p6; two microchaetae appear beside p5. The number and position of s-chaetae remain unchanged. + + +Third instar ( +Fig. 4A +). A secondary mesochaeta appears externally to p6. Other chaetae remain unchanged. + + +Fourth instar ( +Fig. 4B +). A secondary mesochaeta appears beside p6. Other chaetae remain unchanged. + + +Adult macrochaetotaxy ( +Fig. 11A +). Chaetae m2–4 are macrochaetae. Patterns of other chaetae are not determined. + + +Abd. II: +First instar ( +Fig. 3A +). The chaetotaxy is almost identical to that of Abd. I, except that row a has one more mesochaeta (a6). + + +Second instar ( +Fig. 3B +). Mesochaetae become microchaetae except for a6, p5, and p6. A secondary mesochaeta p5e appears between p5 and p6. Two secondary microchaetae appear between a6 and p5, and between m4 and p5, respectively. The number and position of s-chaetae remain almost unchanged, except that the most lateral one is placed more anteriorly. + + +Third instar ( +Fig. 4A +). Chaeta a6 is moved forward. Secondary chaeta p5e becomes a microchaeta. Additional mesochaetae appear on the lateral side. An additional microchaeta appears externally to p5e. Other chaetae remain unchanged. + + +Fourth instar ( +Fig. 4B +). No significant changes occur except that a secondary microchaeta appears anteriorly to m3. + + +Adult macrochaetotaxy ( +Fig. 11A +). Chaetae m2–4 are macrochaetae. Patterns of other chaetae are not determined. + + +Abd. III: +First instar ( +Fig. 3A +). Numbers of chaetae in each row are as follows. Row a: 5; row m: 6 * 1; row p: 6. Chaeta a5 is a bothriotrichum, m3 is a macrochaeta, others are mesochaetae. One s-microchaeta and five normal s-chaetae are present. The s-microchaeta is between m6 and p6. One normal s-chaeta is close to the s-microchaeta, the other four are close to m3, m4, m5, and p3, respectively. The pseudopore is close to m1. + + +Second instar ( +Fig. 3B +). Primary chaetae m6, p1, p3, and p6 become macrochaetae; most mesochaetae become microchaetae except for a7, m7, and p7. About six secondary microchaetae appear in a scattered manner. The number and position of s-chaetae remain unchanged. + + +Third instar ( +Fig. 4A +). Chaetae p6 and p7 are either macro- or mesochaetae. Additional mesochaetae appear on the lateral side. A few more microchaetae are also added. + + +Fourth instar ( +Fig. 4B +). Chaetae a7 and m7 are moved more externally. No other significant changes occur. + + +Adult macrochaetotaxy ( +Fig. 11A +). Chaetae m3, m6, p1, p3, p6, and p7 are macrochaetae; a5 is a bothriotrichum. Patterns of other chaetae are not determined. + + +Abd. IV: +First instar ( +Fig. 3A +). Numbers of chaetae in each row +are as follows. Row a: 7; row m: 7 * 3; row p: 7 * 4. Chaeta a2 and a5 are bothriotricha, m6 and p7 are macrochaetae, +others are mesochaetae. About 26–32 normal and 19–23 long s-chaetae are present. Lengths of the long s-chaetae gradually increase from the anterior ones to the posterior ones. The five longest (longer than Abd. +V +) and most posterior s-chaetae are each associated with a mesochaeta in row p (p1–5). The pseudopore is close to ap1. + + + +Figure 3. +Tergal chaetotaxy of + +Tomocerus tropicus + +. A, First instar; (B) second instar. Open circle with a slash: pseudopore, the same in following figures. + + + + +Figure 4. +Tergal chaetotaxy of + +Tomocerus tropicus + +. A, Third instar; (B) fourth instar. Half black half white circle (e.g., m4 on Th. II in Fig. 4A): chaetae that are either macro- or mesochaetae. + + + +Second instar ( +Fig. 3B +). Primary chaeta p6 becomes a macrochaeta; most mesochaetae become microchaetae except for a7 and m7. Three secondary microchaetae appear near m4, p1, and p6, respectively. The pattern of s-chaetae remains unchanged. + + +Third instar ( +Fig. 4A +). No other significant changes occur than a few added microchaetae. + + +Fourth instar ( +Fig. 4B +). No significant changes occur. In only +one specimen +an additional long s-chaeta appears occasionally beside p4 on one side. + + +Adult macrochaetotaxy ( +Fig. 11A +). Chaetae m6, p6, and p7 are macrochaetae; a2 and a5 are bothriotricha. Patterns of other chaetae are not determined. + + + +Abd. +V +: + +First instar ( +Fig. 3A +). Numbers of chaetae in each row are as follows. Row a: 4; row m: 4; row p: 7. Externolateral chaetae (el) are present. All chaetae in row m are macrochaetae, others are mesochaetae. Seven normal s-chaetae are present, with two in front of row a, three between row a and m, one posterior to p6, and one beside el. The pseudopore is absent. + + +Second instar ( +Fig. 3B +). Most mesochaetae become microchaetae except for p5 and p7. Secondary chaetae appear only at lateral side, including a very lateral macrochaeta. The pattern of s-chaetae remains unchanged. + + +Third instar ( +Fig. 4A +). No significant changes occur. + + +Fourth instar ( +Fig. 4B +). No significant changes occur. + + +Adult macrochaetotaxy ( +Fig. 11A +). Chaetae m2, m3, m5, and m6 are macrochaetae. The secondary lateral macrochaeta is moved further lateral and not considered as a dorsal chaeta. Patterns of other chaetae are not determined. + + + +Abd. +VI +: + +First instar ( +Fig. 3A +). Numbers of chaetae in each row are as follows. Row a: 2; row m: 4; row p: 5. All chaetae in row m are macrochaetae, others are all mesochaetae. No s-chaetae or pseudopore are present. + + +Second instar ( +Fig. 3B +). Chaetae a0, a3, p1, and p4 become microchaetae. + + +Third instar ( +Fig. 4A +). No significant changes occur. + + +Fourth instar ( +Fig. 4B +). A microchaeta is added between p3 and p4. + +The adult macrochaetotaxy is not observed. + +S-chaetotaxy from Th. II to Abd. +V + +Normal s-chaetae: 12–16/6/5/5/5/26–32 * 19–23 (long)/7 +S-microchaetae: 1/1/0/0/1/0/0. + + + \ No newline at end of file diff --git a/data/05/06/2C/05062C5440229E7C05F54C02FACDFAA5.xml b/data/05/06/2C/05062C5440229E7C05F54C02FACDFAA5.xml index 2ae897a925f..ed873ca2d63 100644 --- a/data/05/06/2C/05062C5440229E7C05F54C02FACDFAA5.xml +++ b/data/05/06/2C/05062C5440229E7C05F54C02FACDFAA5.xml @@ -1,62 +1,62 @@ - - - -New deep-sea Atlantic and Antarctic species of Abyssorchomene De Broyer, 1984 (Amphipoda, Lysianassoidea, Uristidae) with a redescription of A. abyssorum (Stebbing, 1888) + + + +New deep-sea Atlantic and Antarctic species of Abyssorchomene De Broyer, 1984 (Amphipoda, Lysianassoidea, Uristidae) with a redescription of A. abyssorum (Stebbing, 1888) - - -Author + + +Author -Hendrycks, Ed A. -2FAD7817-1822-49F7-BAD6-2F2DB632747A -Canadian Museum of Nature, Research and Collections, P. O. Box 3443, Station D, Ottawa, K 1 P 6 P 4, Canada. -ehendrycks@nature.ca +Hendrycks, Ed A. +2FAD7817-1822-49F7-BAD6-2F2DB632747A +Canadian Museum of Nature, Research and Collections, P. O. Box 3443, Station D, Ottawa, K 1 P 6 P 4, Canada. +ehendrycks@nature.ca - - -Author + + +Author -Broyer, Claude De -970067BF-A792-48A9-B32A-B91F0E41C354 -Royal Belgian Institute of Natural Sciences, rue Vautier 29, B- 1000 Bruxelles, Belgium. -cdebroyer@naturalsciences.be +Broyer, Claude De +970067BF-A792-48A9-B32A-B91F0E41C354 +Royal Belgian Institute of Natural Sciences, rue Vautier 29, B- 1000 Bruxelles, Belgium. +cdebroyer@naturalsciences.be -text - - -European Journal of Taxonomy +text + + +European Journal of Taxonomy - -2022 - -2022-06-21 + +2022 + +2022-06-21 - -825 + +825 - -1 -76 + +1 +76 - -http://dx.doi.org/10.5852/ejt.2022.825.1829 + +http://dx.doi.org/10.5852/ejt.2022.825.1829 -journal article -79173 -10.5852/ejt.2022.825.1829 -dda871e8-9212-484c-83be-c68d5536e571 -2118-9773 -6686625 -2AA16E5D-428F-4827-9944-E2EDC3CF90FD +journal article +79173 +10.5852/ejt.2022.825.1829 +dda871e8-9212-484c-83be-c68d5536e571 +2118-9773 +6686625 +2AA16E5D-428F-4827-9944-E2EDC3CF90FD - + Key to the species of the -Abyssorchomene abyssorum +Abyssorchomene abyssorum complex diff --git a/data/40/5B/B8/405BB887E4495F4BBDD520C29102F044.xml b/data/40/5B/B8/405BB887E4495F4BBDD520C29102F044.xml new file mode 100644 index 00000000000..3dcd4fb2dfb --- /dev/null +++ b/data/40/5B/B8/405BB887E4495F4BBDD520C29102F044.xml @@ -0,0 +1,817 @@ + + + +Metalacurbs foordi sp. nov., a new Lacurbsinae (Opiliones, Laniatores, Biantidae) from Ankasa National Park, Ghana + + + +Author + +Pérez-González, Abel +0000-0002-4245-3302 +División Aracnología, Museo Argentino de Ciencias Naturales “ Bernardino Rivadavia ” – CONICET, Av. Ángel Gallardo 470, C 1405 DJR, Buenos Aires, Argentina + + + +Author + +Mamani, Vanesa +0000-0001-9748-5339 +División Aracnología, Museo Argentino de Ciencias Naturales “ Bernardino Rivadavia ” – CONICET, Av. Ángel Gallardo 470, C 1405 DJR, Buenos Aires, Argentina & Departamento de Biodiversidad y Biología Experimental, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Av. Int. Güiraldes s / n, Ciudad Universitaria, C 1428 EHA, Buenos Aires, Argentina + +text + + +African Invertebrates + + +2024 + +2024-12-04 + + +65 + + +2 + + +199 +211 + + + +journal article +10.3897/afrinvertebr.65.138398 +45BDCA97-EB71-44AF-AFE4-47CD13CFD787 + + + + + +Metalacurbs foordi + +sp. nov. + + + + +Figs 1 +, +2 +, +3 +, +4 +, +5 +, +6 +, +7 + + + + +Material examined. + + + +Type material: + + +Holotype + +: +Ghana +• +1 ♂ +; +Western Region +, +Ankasa National Park +; [ + +5.2172 +, +- 2.6514 + +]; + +180 m +a. s. l. + +; + +22 Feb 2013 + +; +B. A. Huber +leg. +; forest near entrance, day collecting; ( +ZFMK +Op 835). + + + + + + +Etymology. + +Patronym in honour of our dear and long-time good friend, the late Stefan Foord (1971–2023), in recognition of a productive, passionate and dedicated life to the research and development of African Arachnology; name in the genitive case. + + + +Diagnosis. + + +The new species can be easily distinguished not only from the other species in the genus, but also from all species of +Lacurbsinae +by the presence, in males, of basally enlarged metatarsus II (Fig. +4 D +) and a dorsal spiniform apophysis on femur IV (Fig. +6 A – D +). Only + +Metalacurbs oedipus +( +Roewer, 1958 +) + +and + +Metalacurbs villiersi +( +Roewer, 1953 +) + +exhibit a tibia IV stout and enlarged as in + +Metalacurbs foordi + +sp. nov. +, but the tibia IV outline and armature are completely different amongst these three species (compare Fig. +6 A – C, E +versus +Roewer 1953: 620 +, fig. 5 and +Roewer 1958: 236 +, fig. 4). + + + + +Description. + + + +Male +holotype +( +ZFMK +Op 835) + +. Body measurements: Total body length 2.78, carapace length 0.73, +scutum magnum +length 2.30, carapace maximum width 1.14, abdominal +scutum +maximum width 1.81. Appendage measurements in Table +1 +. + + + + + + +Appendage measurements (in mm) of + +Metalacurbs foordi + +sp. nov. +, holotype male (ZFMK Op 835). Tr – Trochanter, Fe – Femur, Pa – Patella, Ti – Tibia, Mt – Metatarsus, Ta – Tarsus, T – Total. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
-TrFePaTiMtTaT
+Pedipalp +0.341.881.290.86–0.554.92
Leg I0.311.300.481.011.761.075.93
Leg II0.422.770.762.133.222.4511.76
Leg III0.351.680.531.222.311.267.35
Leg IV0.632.970.862.422.431.57 +10.88 +
+ + +Dorsum +: Outline with a theta (θ) shape, campaniform (bell-shaped) (Figs +1 A +, +2 A +). Carapace wider than long, with a small and rounded frontal hump; anterior border slightly convex (Figs +1 A +, +2 A +). Cheliceral sockets not marked (Fig. +2 A +). Eyes separated, eye mounds high along the mid-line of the carapace; interocular area is smooth with a small transversal elevation (Figs +1 A, E +, +2 A +). Carapace straight in lateral view (Fig. +1 E +). Abdominal +scutum +convex in lateral view (Fig. +1 E +). Sulcus I deep and well-marked, in dorsal view medially slightly curved to posterior body region (Fig. +2 A +). Mesotergal areas defined; sulci II – +V +notably wide, shallow and complete (Figs +1 A +, +2 A +). Mesotergal area I larger than mesotergal areas II – IV (Figs +1 A +, +2 A +). Mesotergal areas I – II with two lateral tubercles; mesotergal area IV with two medial tubercles; tubercles of mesotergal area II longer than tubercles of mesotergal areas I and IV; mesotergal area III with two medial long spiniform apophyses (Figs +1 A, E, F +, +2 A +). Mesotergal area +V +with a row of five small pointed tubercles (Figs +1 G +, +2 A +). Lateral borders of abdominal +scutum +with a row of rounded granules, but at level of posterior mesotergal area II and anterior mesotergal area III with larger tubercles (Figs +1 A +, +2 A +). Free tergite I with a row of six tubercles, with the two most lateral tubercles longer than medial ones; free tergite II with a row of seven tubercles; free tergite III with a row of lateral tubercles and one medial spiniform apophysis [broken] (Figs +1 A, E – G +, +2 A +). + + + + + + + +Metalacurbs foordi + +sp. nov. +, holotype male (ZFMK Op 835), habitus photos +A +dorsal view +B +ventral view +C +ventral view with detail of coxae I – III +D +ventral view with detail of coxa IV and free sternites +E +lateral view +F +posterior view +G +detail of free tergites I – III and anal operculum. Black arrows indicate spiniform apophyses. Scale bars: 1 mm ( +A, B, E +); 500 µm ( +C, D, F, G +). + + + + + + + + +Metalacurbs foordi + +sp. nov. +, holotype male (ZFMK Op 835), drawings of habitus, chelicera and pedipalp +A +habitus, dorsal view +B, C +left chelicera +B +ectal view +C +frontal view +D – F +left pedipalp +D +mesal view +E +ectal view +F +femur, ventral view. Spiniform apophyses in green. Scale bars: 500 μm. + + + +Venter +: Coxa I with setiferous granules (Fig. +1 B, C +); anterior and posterior borders of coxa III with a row of granules connecting with coxae II and IV, respectively; posterior granules of coxa III larger than anterior granules (Fig. +1 B – D +); free sternites with a row of setiferous granules (Fig. +1 D, F, G +); anal operculum with two small tubercles (Fig. +1 E – G +). Spiracles not concealed (Fig. +1 D +). + + +Chelicerae +: Basichelicerite unarmed, with an elongated and slightly marked +bulla +(Fig. +2 B +). Cheliceral hand with sparse setae and rounded frontal setiferous granules (Fig. +2 B, C +). Fixed and movable finger with a row of conical teeth (Fig. +2 C +). + + +Pedipalps +: Raptorial, with spines concentrated on tibia and tarsus (Fig. +2 D, E +). Coxa elongated, slightly shorter than basichelicerite; proximally with one dorsomesal and one dorsoectal granule; ventrally with small granules (Figs +1 A – C +, +2 A +). Trochanter rounded. Femur straight; ventrally with a row of four proximomedial pointed tubercles and one mesal spine in the third proximal region (Fig. +2 D – F +). Patella elongated ventrodistally with one ectal pointed tubercle and one mesal spine (Fig. +2 D, E +). Tibia ventrally with four ectal spines followed by a pointed setiferous tubercle (Fig. +2 E +) and three mesal spines (Fig. +2 D +). Tarsus shorter than tibia; ventrally armed with two ectal and two mesal spines (Fig. +2 D, E +). Claw elongated and pointed (Fig. +2 D +). + + +Legs +: Coxa IV with prolateral pointed setiferous tubercles and two spiniform apophyses, one distal and one subdistal (Figs +1 A, B, D, F +, +2 A +). Trochanter II with one dorsal tubercle (Fig. +4 A, B +); trochanter IV apically with one retrolateral and one prolateral spiniform apophysis (Figs +1 F +, +6 A – D +). Femur I unarmed (Fig. +3 A, B +); femur II with a dorsal row of short tubercles (Fig. +4 B +); femur III with a row of longer dorsal pointed tubercles than in femur II (Fig. +5 B +); femur IV distally slightly thickened, armed with longitudinal rows of pointed tubercles on all surfaces; ventrodistal tubercles longer; dorsally with one spiniform apophysis at the beginning of the distal third and one spiniform apophysis on the distal edge; ventrally with a prolateral subdistal spiniform apophysis (Fig. +6 A – D +). Patellae I – II unarmed (Figs +3 A, B +, +4 A, B +); patella III with dorsal tubercles, the most distal longer and sharp-pointed (Fig. +5 A – C +); patella IV with sharp-pointed tubercles, the most distal tubercles longer (Fig. +6 A – E +). Tibiae I – II unarmed (Figs +3 C +, +4 C +); tibia III with a dorsoproximal tubercle (Fig. +5 C +); tibia IV ventrally enlarged, dorsally with four proximal tubercles, followed by small tubercles decreasing in size, distally with a prolateral and retrolateral pointed tubercle; ventral surface with a row of prolateral tubercles increasing in size, followed by a curved, strong and pointed prolateral apophysis and by a short conical and blunt-tipped apophysis; ventrodistally with two retrolateral short blunt-tipped apophyses (Fig. +6 A – C, E +). Metatarsi I and III thin and unarmed, with pseudoarticular rings (Figs +3 D +, +5 D +); metatarsus II unarmed, proximally swollen (obclavate) and distally thin with pseudoarticular rings (Fig. +4 D +); metatarsus IV proximally broadened, ventroproximally with conical tubercles; dorsoproximally with three pointed tubercles (Fig. +6 A – C, F +). Tarsi III – IV with a dense scopula (Figs +5 E +, +6 G +). Tarsal formula: 4 (2): 9–10 (3): 5: 6 (Figs +3 E +, +4 E +, +5 E +, +6 G +). + + + + + + + +Metalacurbs foordi + +sp. nov. +, holotype male (ZFMK Op 835), right leg I, photos +A +retrolateral view +B +detail of trochanter, femur and patella +C +detail of tibia +D +detail of metatarsus +E +detail of tarsus. Scale bars: 1 mm ( +A +); 500 µm ( +B, D +); 200 µm ( +C, E +). + + + + + + + + +Metalacurbs foordi + +sp. nov. +, holotype male (ZFMK Op 835), right leg II, photos +A +retrolateral view +B +detail of trochanter, femur and patella +C +detail of tibia +D +detail of metatarsus +E +detail of tarsus. Arrow indicates the proximally swollen metatarsus II. Scale bars: 1 mm ( +A, D +); 500 µm ( +B, C, E +). + + + + + + + + +Metalacurbs foordi + +sp. nov. +, holotype male (ZFMK Op 835), right leg III, photos +A +retrolateral view +B +detail of trochanter, femur and patella +C +detail of tibia +D +detail of metatarsus +E +detail of tarsus. Scale bars: 1 mm ( +A +); 500 µm ( +B – D +); 200 µm ( +E +). + + + + + + + + +Metalacurbs foordi + +sp. nov. +, holotype male (ZFMK Op 835), drawings and photos of left leg IV +A +prolateral view +B +retrolateral view +C +prolateral view +D +detail of trochanter, femur and patella +E +detail of tibia +F +detail of metatarsus +G +detail of tarsus. Spiniform apophysis in green. Arrow indicates a pseudoarticular ring. Scale bars: 1 mm ( +A – C +); 500 µm ( +D – F +); 200 µm ( +G +). + + + +Colour +(specimen preserved in 80 % ethanol): General body appearance yellowish-brown; carapace and coxae I – III with dark reticulations; mesotergal areas I – IV, lateral border of +scutum magnum +, posterior border of area +V +and free tergites I – III darker; posterior border of stigmatic area and free sternites dark yellowish-brown (Fig. +1 A – G +); lighter colouration at the level of cheliceral insertion, creating a false appearance of a marked cheliceral socket; pseudoarticular rings lighter (Fig. +1 A +). Appendages light yellowish-brown (Fig. +1 A +); trochanters I – IV, distal portion of femora I – IV, patellae I – IV and tibiae IV with dark brown reticulations (Figs +3 A, B +, +4 A, B +, +5 A, B +, +6 C – E +); tibia I – III, proximal portion of metatarsi II, IV dark brown (Figs +3 C +, +4 C, D +, +5 F +, +6 F +). + + +Genitalia +: General shape of penis tubular (Fig. +7 A, E +) apically enlarged (Fig. +7 C, D +), making the +pars basalis +and +pars distalis +clearly defined (Fig. +7 C +). +Pars distalis +with a ventral enlarged, rounded and laterally compressed portion, that connects to a ventral thin and wide +lamina apicalis +; the junction between these two regions forms a semicircular edge (Fig. +7 D +). +Lamina apicalis +with a dorsal pseudotubular-shaped fold (Fig. +7 B, D +); +lamina apicalis +with two ventral pairs of small and acute macrosetae (Fig. +7 F +). +Pars distalis +with a basal pair of lateral small and acute macrosetae, pointed to the apical region, located just below the narrow-rounded portion (Fig. +7 D +). Narrow-rounded portion of +pars distalis +with two ventral and one ventrolateral pair of small, acute macrosetae (Fig. +7 F +). Glans with basal +capsula externa +articulated with the truncus and with a jack-knife movement during the hydraulic expansion. +Capsula externa +as a rigid sclerite (similar to the +stragulum +in + +Zalmoxoidea + +) with two long and curved projections basally fused; apically, each projection with an enlarged laminar portion tapering to a pointing end, extending laterally over the rounded portion of the +pars distalis +(Fig. +7 A, D +); dorsally with a wide mediobasal cleft (leaving part of the +capsula interna +exposed) becoming mediodistally very narrow so that the curved projections are in contact (Fig. +7 B +). +Capsula interna +, barely visible through transparency, rigid, with a stylus and conductors largely fused, only separated at the apical end; conductors with straight apical margin; stylus pointed with a subapical opening of +ductus ejaculatorius +(Fig. +7 B, D +). + + + + + + + +Metalacurbs foordi + +sp. nov. +, holotype male (ZFMK Op 835), penis drawings +A, B +dorsal view +C, D +lateral view +E, F +ventral view. +Lamina apicalis +in orange; +Capsula externa +in magenta; conductors in red (dashed line); stylus in green (solid and dashed line). Abbreviation: PB ( +pars basalis +), PD ( +pars distalis +), ms (macroseta). Arrow indicates the semicircular edge formed by the junction between +lamina apicalis +and the narrow-rounded portion of +pars distalis +. Asterisk indicates the narrow-rounded portion of +pars distalis +. Scale bars: 500 μm ( +A, C, E +); 100 μm ( +B, D, F +). + + + +Female. +Unknown. + + + + +Distribution. + + +Known only from the +type +locality (Fig. +8 +). + + + + + + +Geographical distribution of +Lacurbsinae +. + +Eulacurbs paradoxa + +(orange square). + +Lacurbs + +(triangles): + +Lacurbs nigrimana + +(yellow), + +L. spinosa + +(red), + +L. fernandopoensis nomen +nudum + +(magenta), + +Lacurbs +sp. + +(bright-cyan). + +Metalacurbs + +(circles): + +Metalacurbs cornipes + +(black), + +M. foordi + +sp. nov. +(magenta), + +M. oedipus + +(red), + +M. simoni + +(white), + +M. villiersi + +(blue). + +Prolacurbs singularis + +(green inverted triangle). Asterisks indicate the type localities. + + + + + \ No newline at end of file diff --git a/data/90/68/3A/90683A7F7B298D5AFF064002A748F838.xml b/data/90/68/3A/90683A7F7B298D5AFF064002A748F838.xml index e7107460c04..0b87fc96f40 100644 --- a/data/90/68/3A/90683A7F7B298D5AFF064002A748F838.xml +++ b/data/90/68/3A/90683A7F7B298D5AFF064002A748F838.xml @@ -1,62 +1,62 @@ - - - -New species of the cuckoo bee genus Austrosphecodes Michener, 1978 (Hymenoptera: Apoidea: Sphecodini) and a key for Brazilian species + + + +New species of the cuckoo bee genus Austrosphecodes Michener, 1978 (Hymenoptera: Apoidea: Sphecodini) and a key for Brazilian species - - -Author + + +Author -Gonçalves, Rodrigo Barbosa -9DD5F746-8E04-46E3-A03E-AE354265B12D -Laboratório de Abelhas, Departamento de Zoologia, Setor de Ciências Biológicas, Universidade Federal do Paraná, Curitiba, Paraná, Brazil. -goncalvesrb@gmail.com +Gonçalves, Rodrigo Barbosa +9DD5F746-8E04-46E3-A03E-AE354265B12D +Laboratório de Abelhas, Departamento de Zoologia, Setor de Ciências Biológicas, Universidade Federal do Paraná, Curitiba, Paraná, Brazil. +goncalvesrb@gmail.com - - -Author + + +Author -Pereira, Felipe Walter -0C782DCC-BFF2-4DCE-AFE8-99E48C068FCF -Laboratório de Abelhas, Departamento de Zoologia, Setor de Ciências Biológicas, Universidade Federal do Paraná, Curitiba, Paraná, Brazil. -felip3walter@gmail.com +Pereira, Felipe Walter +0C782DCC-BFF2-4DCE-AFE8-99E48C068FCF +Laboratório de Abelhas, Departamento de Zoologia, Setor de Ciências Biológicas, Universidade Federal do Paraná, Curitiba, Paraná, Brazil. +felip3walter@gmail.com -text - - -European Journal of Taxonomy +text + + +European Journal of Taxonomy - -2022 - -2022-05-12 + +2022 + +2022-05-12 - -819 + +819 - -55 -89 + +55 +89 - -http://zoobank.org/9f26a543-1a8a-43bb-8443-ab0e14e11c0c + +http://zoobank.org/9f26a543-1a8a-43bb-8443-ab0e14e11c0c -journal article -55514 -10.5852/ejt.2022.819.1777 -303b5752-420d-4de2-9cf0-9b376acb2c14 -2118-9773 -6544410 -9F26A543-1A8A-43BB-8443-AB0E14E11C0C +journal article +55514 +10.5852/ejt.2022.819.1777 +303b5752-420d-4de2-9cf0-9b376acb2c14 +2118-9773 +6544410 +9F26A543-1A8A-43BB-8443-AB0E14E11C0C Keys of -Austrosphecodes +Austrosphecodes from Brazil diff --git a/data/A7/03/A9/A703A9650D30A400FDAFFB793C1602F5.xml b/data/A7/03/A9/A703A9650D30A400FDAFFB793C1602F5.xml index f0a103b1fb1..8a205e2bb88 100644 --- a/data/A7/03/A9/A703A9650D30A400FDAFFB793C1602F5.xml +++ b/data/A7/03/A9/A703A9650D30A400FDAFFB793C1602F5.xml @@ -1,63 +1,63 @@ - - - -Description of two new species of Oecetis (Trichoptera, Leptoceridae) from Borneo + + + +Description of two new species of Oecetis (Trichoptera, Leptoceridae) from Borneo - - -Author + + +Author -Johanson, Kjell Arne -F2A38CF6-59EB-4F88-BFEB-761DBEA7B01A -Department of Zoology, Swedish Museum of Natural History, Box 50007, 10405 Stockholm, Sweden. -kjell.arne.johanson@nrm.se +Johanson, Kjell Arne +F2A38CF6-59EB-4F88-BFEB-761DBEA7B01A +Department of Zoology, Swedish Museum of Natural History, Box 50007, 10405 Stockholm, Sweden. +kjell.arne.johanson@nrm.se - - -Author + + +Author -Malm, Tobias -4CD5E640-D2F2-4123-913E-E854959424EA -Department of Zoology, Swedish Museum of Natural History, Box 50007, 10405 Stockholm, Sweden. -tobias.malm@nrm.se +Malm, Tobias +4CD5E640-D2F2-4123-913E-E854959424EA +Department of Zoology, Swedish Museum of Natural History, Box 50007, 10405 Stockholm, Sweden. +tobias.malm@nrm.se - - -Author + + +Author -Sjöberg, Tin -F20B3A9C-7173-409D-8C89-92977B6D2B8D -Department of Zoology, Swedish Museum of Natural History, Box 50007, 10405 Stockholm, Sweden. -tin.sjoberg@nrm.se +Sjöberg, Tin +F20B3A9C-7173-409D-8C89-92977B6D2B8D +Department of Zoology, Swedish Museum of Natural History, Box 50007, 10405 Stockholm, Sweden. +tin.sjoberg@nrm.se -text - - -European Journal of Taxonomy +text + + +European Journal of Taxonomy - -2022 - -2022-05-18 + +2022 + +2022-05-18 - -819 + +819 - -158 -165 + +158 +165 -journal article -55464 -10.5852/ejt.2022.819.1787 -0f6a0aa7-3aaa-4d95-a674-2327ec91945a -2118-9773 -6564531 -80DE5F71-8A1C-472F-9205-F956639D0605 +journal article +55464 +10.5852/ejt.2022.819.1787 +0f6a0aa7-3aaa-4d95-a674-2327ec91945a +2118-9773 +6564531 +80DE5F71-8A1C-472F-9205-F956639D0605 - + @@ -134,7 +134,7 @@ by the more strongly curved tergum X in lateral view. - + Holotype @@ -146,7 +146,7 @@ by the more strongly curved tergum X in lateral view. , Tawau , -Maliau Basin +Maliau Basin , Nepenthes Camp , @@ -156,11 +156,10 @@ by the more strongly curved tergum X in lateral view. , 116°52′40.7″ E ; - + 994 m -a.s.l. -; +a.s.l.; 9–14 Dec. 2007 @@ -169,10 +168,7 @@ a.s.l. and N. Jönsson leg.; - -6 m -Malaise trap - +6 m Malaise trap , loc# VKBS-2007-27 ; DNA voucher JL5; @@ -207,7 +203,7 @@ Malaise trap MALAYSIA • -1 ♂ +1 ♂ (in alcohol); same collection data as for holotype; DNA voucher JO7; NHRS diff --git a/data/A9/68/87/A96887DAAC6BFFB65771FA8EFF6DFEFE.xml b/data/A9/68/87/A96887DAAC6BFFB65771FA8EFF6DFEFE.xml index e05d8d1d18e..48df15fd93a 100644 --- a/data/A9/68/87/A96887DAAC6BFFB65771FA8EFF6DFEFE.xml +++ b/data/A9/68/87/A96887DAAC6BFFB65771FA8EFF6DFEFE.xml @@ -1,57 +1,57 @@ - - - -A review of Atlantic deep-water species in the genus Talassia (Caenogastropoda, Vanikoridae) + + + +A review of Atlantic deep-water species in the genus Talassia (Caenogastropoda, Vanikoridae) - - -Author + + +Author -Hoffman, Leon -55E2A441-915A-4EB0-B3DC-4A2CD03B1844 -Senckenberg am Meer, Südstrand 40, D- 26382 Wilhelmshaven, Germany. -Leon.Hoffman@Senckenberg.de +Hoffman, Leon +55E2A441-915A-4EB0-B3DC-4A2CD03B1844 +Senckenberg am Meer, Südstrand 40, D- 26382 Wilhelmshaven, Germany. +Leon.Hoffman@Senckenberg.de - - -Author + + +Author -Freiwald, André -0CA1E3B2-FC66-4E22-A02B-FC29F4D7D71B -Senckenberg am Meer, Südstrand 40, D- 26382 Wilhelmshaven, Germany. & Andre. -Andre.Freiwald@Senckenberg.de +Freiwald, André +0CA1E3B2-FC66-4E22-A02B-FC29F4D7D71B +Senckenberg am Meer, Südstrand 40, D- 26382 Wilhelmshaven, Germany. & Andre. +Andre.Freiwald@Senckenberg.de -text - - -European Journal of Taxonomy +text + + +European Journal of Taxonomy - -2022 - -2022-05-17 + +2022 + +2022-05-17 - -819 + +819 - -140 -157 + +140 +157 - -http://zoobank.org/1bed4f4b-ed7a-43cb-abc5-0173d7f93c41 + +http://zoobank.org/1bed4f4b-ed7a-43cb-abc5-0173d7f93c41 -journal article -55465 -10.5852/ejt.2022.819.1785 -6d7f3cbe-c093-4104-aae2-f6bdb2fc017d -2118-9773 -6564545 -1BED4F4B-ED7A-43CB-ABC5-0173D7F93C41 +journal article +55465 +10.5852/ejt.2022.819.1785 +6d7f3cbe-c093-4104-aae2-f6bdb2fc017d +2118-9773 +6564545 +1BED4F4B-ED7A-43CB-ABC5-0173D7F93C41 - + @@ -132,13 +132,15 @@ . - -WESTERN SLOPE + +WESTERN SLOPE , FLORIDA , USA -• 1 shell; +• +1 shell +; 26.3370° N , 84.7598° W @@ -150,12 +152,14 @@ 27 Mar. 2012 -; grab in coral fragments; MSM20/4-GeoB16337-2; +; grab in coral fragments; +MSM20/4-GeoB16337-2 +; SaM • - -1 shell + +1 shell ; 26.4204° N ,