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Fig. 11 in Systematic Review of Endemic Sulawesi Squirrels (Rodentia, Sciuridae), with Descriptions of New Species of Associated Sucking Lice (Insecta, Anoplura), and Phylogenetic and Zoogeographic Assessments of Sciurid Lice
Fig. 11. Collection localities for samples of four species in the Prosciurillus leucomus group: P. leucomus, P. alstoni, P. weberi, and P. topapuensis. The collection site for Prosciurillus sp., which is represented by a subfossil fragment, is also indicated. Distribution of the fifth member, P. rosenbergii, in Kepulauan Sangihe is portrayed on the map in figure 28. Numbers key to localities described in the gazetteer where specimens are also identified by museum initials and catalog numbers. The inset map, right (rectangle in larger map, above), contains collection sites (1–12) for P. topapuensis scattered along Musser's transect from the Sungai Miu to Gunung Nokilalaki. The dashed contour line at 1300 m marks the approximate boundary between tropical lowland evergreen rain forest and tropical lower montane forest.
Fig. 15 in Systematic Review of Endemic Sulawesi Squirrels (Rodentia, Sciuridae), with Descriptions of New Species of Associated Sucking Lice (Insecta, Anoplura), and Phylogenetic and Zoogeographic Assessments of Sciurid Lice
Fig. 15. Specimen scores representing two population samples of Prosciurillus leucomus projected onto the first and second principal components extracted from principal-components analysis. Symbols identifying samples are: filled circle 5 northeastern peninsula (Likupang, Teteamoet, Rurukan, Temboan; N 5 18); X 5 western segment of northern peninsula (Bumbulan, Sungai Paleleh, Gunung Ile-Ile, Labuan Sore, Bumbarujaba; N 5 8). Ellipses outline 95% confidence limits for the specimen scores representing each population sample. See table 18 for correlations and percent variance.
Fig. 12 in Systematic Review of Endemic Sulawesi Squirrels (Rodentia, Sciuridae), with Descriptions of New Species of Associated Sucking Lice (Insecta, Anoplura), and Phylogenetic and Zoogeographic Assessments of Sciurid Lice
Fig. 12. Dorsal views of skulls representing species of Prosciurillus. Top row, left to right: P. alstoni (AMNH 226076; Kuala Navusu; ONL 5 46.6 mm) and P. topapuensis (AMNH 225504; Gunung Kanino; ONL 5 45.0 mm); we employ these two as exemplars of species in the P. leucomus group. Bottom row, left to right: P. abstrusus (AMNH 101378, holotype; Pegunungan Mekongga; ONL 5 38.2 mm) and P. murinus (AMNH 225496; Gunung Kanino; ONL 5 34.4 mm); these are the only species comprising the P. murinus group.
Fig. 16 in Systematic Review of Endemic Sulawesi Squirrels (Rodentia, Sciuridae), with Descriptions of New Species of Associated Sucking Lice (Insecta, Anoplura), and Phylogenetic and Zoogeographic Assessments of Sciurid Lice
Fig. 16. Reproduction of Anderson's (1879) color plate of ''Sciurus alstoni'' (5 Prosciurillus alstoni).
Figure 2 in A new species of the genus Eremochorus Zaslavskij, 1962 (Coleoptera: Curculionidae) from Central Altai (Russia) with systematics remarks
Figure 2. Distribution of Eremochorus spp.: black circle – E. mniszechi, red circle – E. kalashiani sp. nov.
Figures 5-9 in On the the systematics of the water mite Lebertia gibberipalpis Sokolow, 1948 (Acari, Hydrachnidia, Lebertiidae)
Figures 5-9. Lebertia (Mixolebertia) gibberipalpis, female: 5 - genital field; 6 - gnathosoma and chelicera, lateral view; 7- I-Leg-4-6; 8 - IV-Leg-4-6; 9 - claw of leg IV. Scale bars: 5-7, 8 = 100 μm, 9 = 50 μm.
Figures 1-4 in On the the systematics of the water mite Lebertia gibberipalpis Sokolow, 1948 (Acari, Hydrachnidia, Lebertiidae)
Figures 1-4. Lebertia (Mixolebertia) gibberipalpis, female: 1 - fragment of dorsal surface; 2 - seta Fch; 3 - coxal plates and genital field; 4 - pedipalp; Scale bars: 1-2 = 100 μm, 3 = 200 μm, 4 = 50 μm.
Figures 1–8 in On the systematic position of the genus Proaegeria Le Cerf 1916 (Lepidoptera: Sesiidae) with description of a new species
Figures 1–8. Moths. Proaegeria murzini sp. n.: 1–2. Holotype, male, Sesiidae pictures №№ 0023-0024–2023; 3–4. Paratype, male. Sesiidae pictures №№ 0021-0022–2023; 5–6. Paratype, male. Sesiidae pictures №№ 0025-0026–2023; 7–8. Paratype, female. Sesiidae pictures №№ 0019-0020–2023. Dorsal view (1, 3, 5, 7) and ventral view (2, 4, 6, 8).
Figures 9–14 in On the systematic position of the genus Proaegeria Le Cerf 1916 (Lepidoptera: Sesiidae) with description of a new species
Figures 9–14. Genitalia. Proaegeria murzini sp. n.: 9–14. Paratype, male, genitalia preparation № 010–2023. 9. Tegumen-uncus complex; 10. Valva; 11. Saccus; 12. Juxta, ventral view; 13. Phallus. 14. Paratype, female, genitalia preparation № 011–2023. Scale bar 1.0 mm.
Fig. 1 in From incidental findings to systematic discovery: locating and monitoring a new population of the endangered Harlequin Toad
Fig. 1 Location and boundaries of the Alexander Skutch Biological Corridor (ASBC) in the province of San José, Costa Rica.
Fig. 3 in From incidental findings to systematic discovery: locating and monitoring a new population of the endangered Harlequin Toad
Fig. 3 Males, females, and juveniles of Atelopus varius found in the Alexander Skutch Biological Corridor. (A) Male found during February surveys. (B) Sleeping male in the leaf litter in the same location of a male in Fig. 2(A). (C) and (E) are juveniles high above the river bank, at least 3–4 m high in the vegetation of the understory, and juvenile (C) is sleeping. (D) A female Harlequin Toad sleeping on the vegetation five m above the river.
Fig. 2 in From incidental findings to systematic discovery: locating and monitoring a new population of the endangered Harlequin Toad
Fig. 2 Detail of Atelopus varius individuals found during February and June 2017 in the ASBC. The left column includes males; the right column includes females. Males (B) and (C) were photographed as found, as were females (E), (G), and (H). Note the spread-out basking position of female (G).
Fig. 76 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)
Fig. 76. Strict consensus of 25,872 most parsimonious trees of 46,520 steps: relationships among dendrobatids. Numbers above branches are Bremer support values. Numbers following terminal names are unique sample identifiers. Terminals without numbers or with alphanumeric identifiers (GenBank numbers) were not sequenced for the present study or Frost et al. (2006) and were taken from GenBank. Unidentified species taken from GenBank are labeled as originally published. Upper right inset shows entire cladogram and corresponding figure numbers, with present view in black.
Fig. 68 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)
Fig. 68. Length variation in character 142, retroarticular process of the mandible. A: nocturnus, AMNH 130041. B: riveroi, AMNH 134142. C: vittatus, AMNH 118386. D: lehmanni Myers and Daly, AMNH118442. E: pratti, AMNH118364. F: ''Neblina species'', AMNH 118667.
Fig. 72 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)
Fig. 72. Strict consensus of 25,872 most parsimonious trees of 46,520 steps: relationships among dendrobatids. Numbers above branches are Bremer support values. Numbers following terminal names are unique sample identifiers. Terminals without numbers or with alphanumeric identifiers (GenBank numbers) were not sequenced for the present study or Frost et al. (2006) and were taken from GenBank. Unidentified species taken from GenBank are labeled as originally published. Upper right inset shows entire cladogram and corresponding figure numbers, with present view in black.
Fig. 74 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)
Fig. 74. Strict consensus of 25,872 most parsimonious trees of 46,520 steps: relationships among dendrobatids. Numbers above branches are Bremer support values. Numbers following terminal names are unique sample identifiers. Terminals without numbers or with alphanumeric identifiers (GenBank numbers) were not sequenced for the present study or Frost et al. (2006) and were taken from GenBank. Unidentified species taken from GenBank are labeled as originally published. Upper right inset shows entire cladogram and corresponding figure numbers, with present view in black.
Fig. 62. Character 105, reproductive amplexus. State 2 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)
Fig. 62. Character 105, reproductive amplexus. State 2, cephalic amplexus (anthonyi, AMNH live exhibit) shown in anterior (A) and lateral (B) aspects.
Fig. 63. Character 109, dorsal larval transport. State 1 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)
Fig. 63. Character 109, dorsal larval transport. State 1, present (fraterdanieli, specimens at UVC). This male nurse frog was transporting 12 tadpoles.
Fig. 57 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)
Fig. 57. Anterior view of the open mouth of the dendrobatid praderioi (CPI 10203) showing the short, tapered median lingual process (MLP).
Fig. 55. Character 70, m. semitendinosus binding tendon. State 1 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)
Fig. 55. Character 70, m. semitendinosus binding tendon. State 1, present (aurotaenia, AMNH 161109), photograph (left) and outline drawing (right) showing view of the concealed surface of the knee. The mm. gracilis complex is deflected ventrally to reveal the dorsad ''ranid'' path of the m. semitendinosus and the secondary binding tendon that straps it to the outer edge of the mm. gracilis complex.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.