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Fig. 4 in Integrative taxonomy reveals unanticipated hidden diversity in the monotypic goosefish genus Lophiomus (Teleostei, Lophiidae), with description of three new species and resurrection of Chirolophius laticeps Ogilby, 1910

Fig. 4. Phylogenetic trees of species of Lophiomus Gill, 1883 reconstructed by partitioned maximumlikelihood and Bayesian inference methods based on the TC dataset (4146 bp, COI: 663 bp; cytb: 1143 bp; RAG1: 1440 bp; Rhodopsin: 900 bp; ML: TN + F + I (partition 1, 1–663), GTR + F + I + G4 (partition 2, 664–1806), TPM3 + F + G4 (partition 3, 1807–3246), TPM2u+F+I (partition 4, 3247–4146); BI: with the same partition but changed to HKY + I (partition 1), GTR + I + G (partition 2), GTR + G (partition 3), GTR+I (partition 4)). Phylogenetic tree branch lengths are proportional to inferred nucleotide substitutions except the connection to distant outgroup Lophiodes mutilus. Node numbers represent 'SH-aLRT / UFBoot / pp.' values, with the former two values expressed in percent (%). See the caption of Fig. 2 for locality abbreviations. Terminal names in bold suggest the newly described or resurrected taxa in this study.

opencc-by-4.0Jul 2024View details →
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Fig. 5 in Integrative taxonomy reveals unanticipated hidden diversity in the monotypic goosefish genus Lophiomus (Teleostei, Lophiidae), with description of three new species and resurrection of Chirolophius laticeps Ogilby, 1910

Fig. 5. PCA biplot of the first and second principal components (PC1 and PC2) of species of Lophiomus Gill, 1883, with a total of 49.2% of explained variation based on 16 measurements and meristic counts (see Results). Ellipses indicate the confidence interval level set at 0.68 for each group. Arrows represent the direction of the variables projected into the 2D plane of PC1 and PC2.

opencc-by-4.0Jul 2024View details →
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Fig. 3 in Integrative taxonomy reveals unanticipated hidden diversity in the monotypic goosefish genus Lophiomus (Teleostei, Lophiidae), with description of three new species and resurrection of Chirolophius laticeps Ogilby, 1910

Fig. 3. Maximum-likelihood phylogenetic tree of species of Lophiomus Gill, 1883 based on the NU dataset (2340 bp, RAG1: 1440 bp;Rhodopsin: 900 bp; TPM3u + F + G4 (1–1440 bp), TPM2u + F + I (1441– 2340 bp)). Phylogenetic tree branch lengths are proportional to inferred nucleotide substitutions except the connection to distant outgroup Lophiodes mutilus. Node numbers represent 'SH-aLRT / UFBoot' values in percent (%). See the caption of Fig. 2 for locality abbreviations. The terminal names in bold suggest the newly described or resurrected taxa in this study.

opencc-by-4.0Jul 2024View details →
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Fig. 1 in Integrative taxonomy reveals unanticipated hidden diversity in the monotypic goosefish genus Lophiomus (Teleostei, Lophiidae), with description of three new species and resurrection of Chirolophius laticeps Ogilby, 1910

Fig. 1. Bathymetric terrain map of eastern Indian Ocean and West Pacific showing the occurrence points of species of Lophiomus Gill, 1883 based on the samples/sequences included in the analyses of this study. White circle: type locality of the species of Lophiomus.

opencc-by-4.0Jul 2024View details →
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Fig. 2 in Integrative taxonomy reveals unanticipated hidden diversity in the monotypic goosefish genus Lophiomus (Teleostei, Lophiidae), with description of three new species and resurrection of Chirolophius laticeps Ogilby, 1910

Fig. 2. Maximum-likelihood phylogenetic tree of the species of Lophiomus Gill, 1883 based on the MT dataset (1806 bp, COI: 663 bp; cytb: 1143 bp; TN + F + I (1–663 bp), GTR + F + I + G4 (664–1806 bp)) with species delimitation analyses (vertical bars on the right side of the tree). Branch lengths of the phylogenetic tree are proportional to the inferred nucleotide substitutions except for the one connecting to the distant outgroup of Lophiodes mutilus. Node numbers represent 'SH-aLRT / UFBoot' values in percent (%). Locality abbreviations: AU = Australia (NSW = New South Wales; Qld = Queensland; WA = Western Australia); CS = Coral Sea; HN = Hainan Island; IN = India; NC = New Caledonia; PH = Penghu Island; PL = Philippine; PNG = Papua New Guinea; SCS = South China Sea; TH = Thailand; TW = Taiwan. Text next to final decisions represents inferred taxon names and numbers of supported criteria covering all available criteria, with proportions in parentheses.

opencc-by-4.0Jul 2024View details →
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Fig. 6. Neopanorpa lungtaushana Cheng, 1957. A, C–I. Male. A. Habitus, dorsal view. C. Head, frontal view. D. T3 and T4 in Taxonomy of the genus Neopanorpa van der Weele, 1909 (Mecoptera, Panorpidae) from the Oriental Region, with the description of two new species

Fig. 6. Neopanorpa lungtaushana Cheng, 1957. A, C–I. Male. A. Habitus, dorsal view. C. Head, frontal view. D. T3 and T4, left-lateral view. E. Epandrium and hypandrium, right-lateral view. F–G. Genital bulb, ventral and dorsal views, respectively. H–I. Aedeagal complex, ventral and rightlateral views, respectively. – B, J–L. Female. B. Habitus, dorsal view. J. Subgenital plate, ventral view. K–L. Medigynium, right-lateral and ventral views, respectively.

opencc-by-4.0Aug 2019View details →
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Fig. 4 in Taxonomy of the genus Neopanorpa van der Weele, 1909 (Mecoptera, Panorpidae) from the Oriental Region, with the description of two new species

Fig. 4. Neopanorpa ocellaris (Navás, 1908), living female. The female is feeding on a dead crane fly. Photo by Wei-Liang Xie from Huanjiang County, Guangxi Province, China.

opencc-by-4.0Aug 2019View details →
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Fig. 2 in Taxonomy of the genus Neopanorpa van der Weele, 1909 (Mecoptera, Panorpidae) from the Oriental Region, with the description of two new species

Fig. 2. Neopanorpa luojishana Wang & Hua sp. nov., paratypes (NWAU). A, C–J. Male. A. Habitus, dorsal view. C. Head, frontal view. D. Abdomen, left-lateral view. E–F. Genital bulb, dorsal and ventral views, respectively. G. Right gonostylus, left-lateral view. H. Epandrium and hypandrium, rightlateral view. I–J. Aedeagal complex, ventral and right-lateral views, respectively. – B, K–L. Female. B. Habitus, dorsal view. K. Subgenital plate, ventral view. L. Medigynium, ventral view.

opencc-by-4.0Aug 2019View details →
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Fig. 5 in Taxonomy of the genus Neopanorpa van der Weele, 1909 (Mecoptera, Panorpidae) from the Oriental Region, with the description of two new species

Fig. 5. Neopanorpa ocellaris (Navás, 1908). A, C–K. Male. A. Habitus, dorsal view. C. Epandrium, dorsal view. D. Head, frontal view. E. T3 and T4, left-lateral view. F. Genital bulb, ventral view. G. Habitus, left-lateral view. H. Left gonostylus, ventral view. I. Epandrium and hypandrium, leftlateral view. J–K. Aedeagal complex, ventral and right-lateral views, respectively. – B, L–N. Female. B. Habitus, dorsal view. L. Subgenital plate, ventral view. M–N. Medigynium, ventral and right-lateral views, respectively.

opencc-by-4.0Aug 2019View details →
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Fig. 1 in Taxonomy of the genus Neopanorpa van der Weele, 1909 (Mecoptera, Panorpidae) from the Oriental Region, with the description of two new species

Fig. 1. Neopanorpa luojishana Wang & Hua sp. nov., living male. Photo by Ji-Shen Wang from Mt. Luoji, Sichuan, China.

opencc-by-4.0Aug 2019View details →
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Fig. 3 in Taxonomy of the genus Neopanorpa van der Weele, 1909 (Mecoptera, Panorpidae) from the Oriental Region, with the description of two new species

Fig. 3. Neopanorpa xingmini Wang & Hua sp. nov., paratypes (NWAU). A, C–L. Male. A. Habitus, dorsal view. C. Head, frontal view. D. Abdomen, left-lateral view. E. Apical portion of epandrium, ventral view. F. Hypovalves, caudal view. G–H. Genital bulb, dorsal and ventral views, respectively. I. Epandrium and hypandrium, right-lateral view. J. Left gonostylus, ventral view. K–L. Aedeagal complex, ventral and right-lateral views, respectively. – B, M–N. Female. B. Habitus, dorsal view. M. Subgenital plate, ventral view. N. Medigynium, ventral view.

opencc-by-4.0Aug 2019View details →
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Figures 7−15 in On the taxonomy of Zeuzera boisduvalii Herrich-Schäffer, 1854 (Cossidae, Zeuzerinae) species complex with description of a new genus and three new species

Figures 7−15. Adult specimens of Davidlivingstonia and their labels: 7. D. staudei Yakovlev spec. nov., holotype (MWM). 8. D. staudei Yakovlev spec. nov., paratype, male, Zambia, Samfia (MWM); 9. D. staudei Yakovlev spec. nov., paratype, male, Democratic Republic of the Congo, 10 km SE Kisangani (MWM); 10. D. staudei Yakovlev spec. nov., paratype, male, Democratic Republic of the Congo, Lokolenge (MRAC); 11. D. prozorovi Yakovlev spec. nov., holotype (NHMUK); 12. D. lenzi Yakovlev spec. nov., holotype (ANHRT); 13. D. lenzi Yakovlev spec. nov., paratype, female, Zambia (ANHRT); 14. D. lenzi Yakovlev spec. nov., paratype, male, Kenya, Sigor (MWM); 15. D. lenzi Yakovlev spec. nov., paratype, male, Tansania, Mpanda (ZSM).

opencc-by-4.0Dec 2020View details →
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Figures 22−24 in On the taxonomy of Zeuzera boisduvalii Herrich-Schäffer, 1854 (Cossidae, Zeuzerinae) species complex with description of a new genus and three new species

Figures 22−24. Genitalia of Davidlivingstonia: 22. D. lenzi Yakovlev spec. nov., paratype, male, Kenya, Sigor, gen. slide Heterocera No.: 32.933 (MWM); 23. D. boisduvalii (Herrich-Schäffer, 1854), female, Côte d'Ivoire, Touba, Biemasso, gen. slide No.: ANHRT 00039 (ANHRT); 24. D. lenzi Yakovlev spec. nov., paratype, female, Zambia, Ndole Bay, on the shores of the Lake Tanganyika, gen. slide No.: ANHRT 00041 (ANHRT). Scale bar = 1 mm.

opencc-by-4.0Dec 2020View details →
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Figures 1−6 in On the taxonomy of Zeuzera boisduvalii Herrich-Schäffer, 1854 (Cossidae, Zeuzerinae) species complex with description of a new genus and three new species

Figures 1−6. Adult specimens of Davidlivingstonia boisduvalii (Herrich-Schäffer, 1854) and their labels: 1. Holotype (MNHN); 2. Male, Sierra Leone (ANHRT); 3. Male, Côte d'Ivoire (ANHRT); 4. Male, Guinea Konakri (coll. G. Müller, Freising); 5. Male, Benin (MNHN); 6. Female, Côte d'Ivoire (ANHRT).

opencc-by-4.0Dec 2020View details →
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Figures 16−21 in On the taxonomy of Zeuzera boisduvalii Herrich-Schäffer, 1854 (Cossidae, Zeuzerinae) species complex with description of a new genus and three new species

Figures 16−21. Male genitalia of Davidlivingstonia: 16. D. boisduvalii (Herrich-Schäffer, 1854), Sierra Leone, Loma Mountains, gen. slide No.: LG 5183 (ANHRT); 17. D. boisduvalii (Herrich-Schäffer, 1854), Côte d'Ivoire, Mt. Tonkoui, gen. slide No.: ANHRT 00038 (ANHRT); 18. D. staudei Yakovlev spec. nov., holotype, Zambia, Samfia, Mukushi, reg. Liubwe, gen. slide Heterocera No.: 32.930 (MWM); 19. D. staudei Yakovlev spec. nov., paratype, Democratic Republic of the Congo, 10 km SE Kisangani, Island Mbiye, Congo River, gen. slide Heterocera No.: 32.932 (MWM); 20. D. prozorovi Yakovlev spec. nov., holotype, male, Congo Belge, Congo River, gen. slide No.: NHMUK 010315467 (NHMUK); 21. D. lenzi Yakovlev spec. nov., holotype, Zambia, Ndole Bay, on the shores of the Lake Tanganyika, gen. slide No.: ANHRT 00040 (ANHRT). Scale bar = 1 mm.

opencc-by-4.0Dec 2020View details →
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Figures 17–20 in On the taxonomy of the Chelis glaphyra (Eversmann, 1843) species-group, with description of a new subspecies of Chelis gratiosa (Grum-Grshimailo, 1890) from Kyrgyzstan, brachipterous females of Chelis kashmirica (Ferguson, 1985) and Chelis golbecki (Dubatolov, 1996), and the checklist of the species-group (Lepidoptera: Erebidae: Arctiinae: Arctiini)

Figures 17–20. Chelis gratiosa sspp.: adults. Depositories of the specimens: 17 in ASV/WIGJ; 18–20 in MWM/ZSM.

opencc-by-4.0Nov 2020View details →
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Figure 29 in On the taxonomy of the Chelis glaphyra (Eversmann, 1843) species-group, with description of a new subspecies of Chelis gratiosa (Grum-Grshimailo, 1890) from Kyrgyzstan, brachipterous females of Chelis kashmirica (Ferguson, 1985) and Chelis golbecki (Dubatolov, 1996), and the checklist of the species-group (Lepidoptera: Erebidae: Arctiinae: Arctiini)

Figure 29. Kyrgyzstan, Transalai Range, Aram-Kungei valley, the type locality of Chelis gratiosa kartashovi (photo by V. Kartashov).

opencc-by-4.0Nov 2020View details →
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Figure 9 in On the taxonomy of the Chelis glaphyra (Eversmann, 1843) species-group, with description of a new subspecies of Chelis gratiosa (Grum-Grshimailo, 1890) from Kyrgyzstan, brachipterous females of Chelis kashmirica (Ferguson, 1985) and Chelis golbecki (Dubatolov, 1996), and the checklist of the species-group (Lepidoptera: Erebidae: Arctiinae: Arctiini)

Figure 9. Chelis gratiosa kartashovi, paratypes. The specimens are deposited in VKV (photo by V. Kartashov).

opencc-by-4.0Nov 2020View details →
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Figures 19-24 in On the taxonomy of Meganola cretacea (Hampson, 1914) with description of two new species (Lepidoptera, Nolidae, Nolinae)

Figures 19-24: male genitalia. 19, Ezishnola cretacea (Hampson, 1914), LGNA 835, Guinea, Nimba Mts (ANHRT); 20, E. cretacea (Hampson, 1914), LGNA 953, Liberia, Nimba Mts (ANHRT); 21, E. inopinata sp. n., paratype, LGNA 60, Zambia, Lukwakwa (ANHRT); 22, E. inopinata sp. n., paratype, LGNA 292, Zambia, Ikelenge (ANHRT); 23, E. carcassoni sp. n. paratype, NHMUK 010316558 (Gy. M. László), Uganda, Masaka (NHMUK); 24, E. fuscographa László, Ronkay & Witt, 2010, holotype, LGN 953, Thailand, Pua (MWM/ZSM).

opencc-by-4.0Apr 2020View details →
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Figures 17–20 in On the taxonomy of the Oriental genus Paraona Moore with descriptions of a new genus, a new species, and introduction of new synonymies (Lepidoptera: Erebidae: Arctiinae: Lithosiini)

Figures 17–20. Murmyshia spp.: male genitalia. Depositories of the specimens dissected: 17 and 19 in MWM/ZSM; 18 and 20 in CKC.

opencc-by-4.0Jun 2024View details →

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International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
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