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Figure 8 in The otic region of Doleserpeton (Temnospondyli) and its implications for the evolutionary origin of frogs
Figure 8. Posterior part of the braincase of Doleserpeton, specimen UR1333, in medial view. Part of the anterior edge of the jugular foramen has been reinforced with glue.
Figure 7 in The otic region of Doleserpeton (Temnospondyli) and its implications for the evolutionary origin of frogs
Figure 7. Right opisthotic of Doleserpeton, specimen UR1317. A, posterior view; B, anterior view. Sharp edges are drawn in solid lines, whereas impressions, convexities, and concavities of the bone are stippled.
Figure 6 in The otic region of Doleserpeton (Temnospondyli) and its implications for the evolutionary origin of frogs
Figure 6. Right prootic of Doleserpeton, specimen UR1314. A, anterior view; B, posterior view. Sharp edges are drawn in solid lines, whereas impressions, convexities, and concavities of the bone are stippled.
Figure 5 in The otic region of Doleserpeton (Temnospondyli) and its implications for the evolutionary origin of frogs
Figure 5. Braincase and otic region of Doleserpeton, specimen UR1322. A, occipital view. B, right side in ventral view.
Figure 4 in The otic region of Doleserpeton (Temnospondyli) and its implications for the evolutionary origin of frogs
Figure 4. The perilymphatic systems of Latimeria and tetrapods. Schematic figures of otic capsules oriented in such a way that the anterior is to the right and the lateral is upwards in the drawings. Modified from Lombard (1980) and Fritzsch (1992).
Figure 3 in The otic region of Doleserpeton (Temnospondyli) and its implications for the evolutionary origin of frogs
Figure 3. The inner ear of lissamphibians (not drawn to scale). A, Ascaphus truei, dorsal view, left side. B, Ascaphus truei, ventral view, right side. C, Hynobius nigricens, dorsal view, left side. D, Caecilia occidentalis, dorsal view, left side. From Lombard (1977).
Figure 2 in The otic region of Doleserpeton (Temnospondyli) and its implications for the evolutionary origin of frogs
Figure 2. The occiputs of extant and fossil lissamphibians (not drawn to scale). A, Conraua goliath (from Starck, 1979). B, unidentified pipid anuran from the Upper Cretaceous In Beceten locality (from Baez & Rage, 1998). C, Cryptobranchus alleganiensis (from Carroll & Holmes, 1980). D, Hynobius naevius (from Carroll & Holmes, 1980). E, Hypogeophis rostratus (from Carroll & Currie, 1975). F, Eocaecilia micropodia (from Jenkins, Walsh & Carroll, 2007).
Figure 1 in The otic region of Doleserpeton (Temnospondyli) and its implications for the evolutionary origin of frogs
Figure 1. The otic region of Rana catesbeiana. A, right posterior part of the braincase, in ventral view. B, right side of the braincase, in posterior view (based on several specimens).
Figure 5. A in Biogeographical analysis of Cameroonian puddle frogs and description of a new species of Phrynobatrachus (Anura: Phrynobatrachidae) endemic to Mount Oku, Cameroon
Figure 5. A, map illustrating topography of Cameroon and neighbouring countries. Inset shows position of Cameroon within Africa. Black star indicates position of Mt Oku. B, topographic map of portion of Bamenda Highlands (magnification of rectangle in Fig. 3A), showing the single known locality of Phrynobatrachus chukuchuku sp. nov. at Mt Oku (black star). Black circle indicates position of Lake Oku.
Figure 4 in Biogeographical analysis of Cameroonian puddle frogs and description of a new species of Phrynobatrachus (Anura: Phrynobatrachidae) endemic to Mount Oku, Cameroon
Figure 4. Variation of interorbital line and dorsal head coloration amongst paratypes of Phrynobatrachus chukuchuku sp. nov. A, MCZ A-138124, B, MCZ A-138125, C, MCZ A-138126, D, MCZ A-138129, E, MCZ A-138130, F, MCZ A-138132. Scale bars = 1 mm.
Figure 3 in Assessing the taxonomic status of tropical frogs through bioacoustics: geographical variation in the advertisement calls in the Eleutherodactylus discoidalis species group (Anura)
Figure 3. Discriminant function analyses of the number of pulses, call length, and dominant frequency of species belonging to the Eleutherodactylus discoidalis group. Ellipses only intend to facilitate the observation of groups. BV, Eleutherodactylus cf. cruralis from the Bellavista Mountains; EC, Eleutherodactylus cruralis; ED, Eleutherodactylus discoidalis; EI, Eleutherodactylus ibischi; HO, Eleutherodactylus cf. cruralis from La Hoyada; EM, Eleutherodactylus madidi.
Figure 2 in Assessing the taxonomic status of tropical frogs through bioacoustics: geographical variation in the advertisement calls in the Eleutherodactylus discoidalis species group (Anura)
Figure 2. Oscillogram and sound spectrogram of the advertisement call of: (A) Eleutherodactylus cruralis from Rurrenabaque, Amazonian rainforest; (B) E. cf. cruralis from Bellavista Mountains; (C) E. cf. cruralis from La Hoyada; (D) Eleutherodactylus discoidalis from Campos de Pinos; (E) Eleutherodactylus ibischi from Samaipata Road; (F) Eleutherodactylus madidi from Eslabón.
Figure 4 in Assessing the taxonomic status of tropical frogs through bioacoustics: geographical variation in the advertisement calls in the Eleutherodactylus discoidalis species group (Anura)
Figure 4. Scatterplot for (A) number of pulses and call length, (B) dominant frequency and number of pulses, and (C) dominant frequency and call length of species and populations of the Eleutherodactylus discoidalis group. Lines correspond to normally distributed probability ellipses (0.99, N = 194). BV, Eleutherodactylus cf. cruralis from the Bellavista Mountains; EC, Eleutherodactylus cruralis; ED, Eleutherodactylus discoidalis; EI, Eleutherodactylus ibischi; HO, Eleutherodactylus cf. cruralis from La Hoyada; EM, Eleutherodactylus madidi.
Figure 1 in Assessing the taxonomic status of tropical frogs through bioacoustics: geographical variation in the advertisement calls in the Eleutherodactylus discoidalis species group (Anura)
Figure 1. Map of the Andes of Bolivia showing the studied localities (see also Table 1). 1, Eslabón; 2, Chalalán; 3, Rurrenabaque; 4, Chapare, 500 m; 5, Mataracú; 6, La Hoyada; 7, Samaipata road; 8, Bellavista Mt; 9, Masicurí; 10, Campos de Pinos.
Figure 24 in Ontogeny of a new Palaeogene pipid frog from southern South America and xenopodinomorph evolution
Figure 24. Ventral view of the suprascapular cartilages and cleithra of two anuran species. A, Pipa pipa (KU 204065). B, Xenopus wittei (KU 195673). Numbers before the colon indicate the character and numbers after the colon indicate the character state. Cartilage is shown in grey, bone is shown in white, and combined grey and stippling denotes invasion of cleithral ossification. Not to scale.
Figure 21 in Ontogeny of a new Palaeogene pipid frog from southern South America and xenopodinomorph evolution
Figure 21. Ventral aspects of the postzygapophyses of three anuran taxa. A, Discoglossus galganoi (MNCN 15143). B, Xenopus laevis (KU 69842). C, Hymenochirus curtipes (KU 204127). Not to scale.
Figure 20 in Ontogeny of a new Palaeogene pipid frog from southern South America and xenopodinomorph evolution
Figure 20. Ventral views (only right sides shown) of the skulls of four anuran taxa. A, Discoglossus sardus (KU 129239). B, Palaeobatrachus sp. redrawn from Báez & Trueb (1997: fig. 11). C, Silurana epitropicalis (KU 195660). D, Rhinophrynus dorsalis (KU 84886). Numbers before the colon indicate the character and numbers after the colon indicate the character state. Foramina are shown in black, cartilage is shown in grey, and bone is shown in white; the pterygoids are stippled. Not to scale.
Figure 16 in Ontogeny of a new Palaeogene pipid frog from southern South America and xenopodinomorph evolution
Figure 16. Posterior views (only right sides shown) of the skulls of three anuran taxa. A, Xenopus laevis (KU 195935). B, 'X.' romeri redrawn from Estes (1975a: fig.1). C, Pipa pipa (KU 129698). Numbers before the colon indicate the character and numbers after the colon indicate the character state. Foramina are shown in black and bone is shown in white. Not to scale.
Figure 12 in Ontogeny of a new Palaeogene pipid frog from southern South America and xenopodinomorph evolution
Figure 12. Sequence of development of Llankibatrachus truebae; all specimens were staged according to the Nieuwkoop & Faber (1956) normal table for Xenopus laevis and are shown in dorsal view. A, Nieuwkoop & Faber Stage 57/58 tadpole (BAR 2477–10). B, Stage 59 tadpole (BAR 1309–10). C, Stage 62 tadpole (BAR 2474–10). D, Stage 65 tadpole (BAR 2606–10). Calcium deposits and bone impressions are shown in stippling; bones are shown in black. Scale bar = 6 mm.
Figure 10 in Ontogeny of a new Palaeogene pipid frog from southern South America and xenopodinomorph evolution
Figure 10. Photographs of Llankibatrachus truebae larvae. A, Nieuwkoop & Faber Stage 57/58 tadpole in ventral view; note the absence of forelimbs. B, Nieuwkoop & Faber Stage 59 (BAR 1309–10) tadpole in dorsal view; note the erupted forelimbs. Scale bars = 2 mm.
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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.