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Figure 14 in Diversity among New World microhylid frogs (Anura: Microhylidae): morphological and osteological comparisons between Nelsonophryne (Günther 1901) and a new genus from Peru
Figure 14. Pelvic girdles of Nelsonophryne. Nelsonophryne aequatorialis (KU 178288) in lateral (A) and dorsal (B) aspects. Nelsonophryne aterrima (KU 30773) in lateral (C) and dorsal (D) aspects. Grey denotes cartilage, and grey with stipples, mineralized cartilage.
Figure 14. Cytochrome b in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)
Figure 14. Cytochrome b tree of the three taxa in the Cettia acanthizoides complex and Cettia cetti albiventris, rooted with Phylloscopus chloronotus, estimated by Bayesian inference under the GTR + I model. Posterior probabilities (81 000 trees) are shown above nodes, and parsimony bootstrap values (1000 replicates) are shown below nodes.
Figures 7–14. Figs 7-9 in Sanitation with sponge and plunger: western Atlantic slit-wormsnails (Mollusca: Caenogastropoda: Siliquariidae)
Figures 7–14. Figs 7-9, Tenagodus modestus, teleoconch detail (Florida Keys, FMNH 296716). 7: transition from shell covering posterior organs (shell slit filled) to posterior mantle cavity region (shell slit narrowed to series of holes). 8: detail of Fig. 7; note regular, layered restrictions. 9: late shell; slit unrestricted. Figs 10–13, Tenagodus squamatus, teleoconch detail (Bahamas, FMNH 296709). 10: transition from shell covering posterior organs (shell slit filled) to posterior mantle cavity region (shell slit open). 11, 12: detail of Fig. 10; note incomplete restrictions when compared to Fig. 8. Fig. 13: adult sculpture; note fluted hollow spines. Fig. 14, Tenagodus barbadensis sp. nov., teleoconch detail (FMNH 301290); early whorls opened to display internal septation by calcareous plugs. All SEM. Scale bars = 300 Mm (Figs 8, 11, 12) and 1 mm (all others).
Figure 14 in The Palaeozoic Ancestry of Salamanders, Frogs and Caecilians
Figure 14. Musculature of the lower jaw and hyoid apparatus associated with feeding in terrestrial salamanders and frogs. A, ventral transverse throat musculature of Ambystoma tigrinum. B, hyobranchial apparatus and longitudinal throat and tongue musculature of Ambystoma tigrinum in ventral view. C–F, mandibular and hyoid musculature of Bufo marinus. C, superficial mandibular musculature, with medial raphe removed in upper right to expose deeper muscles. D, superficial (left) and deeper (right) hyoid musculature. E, tongue muscles. F, deep hyoid muscles (all in ventral view). A, B, reproduced from Larsen & Guthrie (1975). C, F, reproduced from Duellman & Trueb (1986).
Figure 14 in Elasmobranchs from the Lower Triassic Sulphur Mountain Formation near Wapiti Lake (BC, Canada)
Figure 14. Wapitiodus homalorhizo sp. nov.: anterior (A, occlusal view) and posterior (B, labial view, partly as imprint) tooth as preserved in the holotype UALVP 46531. Arrows indicate (from left to right, top to bottom) the longitudinal crest, the labial peg, the asymmetric main cusp and the prominent ridges preserved as imprints.
Figure 14 in Extensive diversification of pebblesnails (Lithoglyphidae: Fluminicola) in the upper Sacramento River basin, northwestern USA
Figure 14. Shells, opercula, and radula of Fluminicola caballensis. A, holotype (USNM 1020675). B, USNM 1020679. C, USNM 1020678. D, USNM 1020680. E–G, USNM 1020676. Scales = 1.0 mm. H, outer side of operculum (USNM 1020676). Scale = 200 µm. I, portion of radular ribbon (USNM 1020676). Scale = 20 µm. J, central radular teeth (USNM 1020676). Scale = 10 µm. K, lateral and marginal radular teeth (USNM 1020676). Scale = 20 µm. L, outer marginal tooth; note absence of wing along outer edge. Scale = 10 µm.
Figure 14 in Osteology and ecology of Megantereon cultridens SE311 (Mammalia; Felidae; Machairodontinae), a sabrecat from the Late Pliocene - Early Pleistocene of Senéze, France
Figure 14. Left humerus and antebrachium and right metacarpals of Megantereon cultridens SE311. Humerus in anterior (A), posterior (B), medial (C) and lateral (D) view; ulna in medial (E), lateral (F) and anterior view (G); radius in lateral (H) and ulnar (I) view; metacarpals I-V in dorsal (J) and palmar (K) view.
Figure 14 in A peculiar climbing Megalonychidae from the Pleistocene of Peru and its implication for sloth history
Figure 14. Drawings of calcaneum and astragalus of Diabolotherium nordenskioldi gen. nov. (MNHN CPN 9–1, referred specimen). A–C, left calcaneum in dorsal (posterior towards the top, medial towards the left), plantar (posterior towards the top, medial towards the right), and anterior (dorsal towards the top, medial towards the left) views, respectively. D–F, left astragalus in anterior (dorsal towards the top, medial towards the left), dorsal (posterior towards the top, medial towards the left), and plantar (posterior towards the top, medial towards the right) views, respectively. ass, astragalar sulcus; asst, astragalar sustentaculum; Astf, astragalar facets; Calf, calcaneal facets; Cubf, cuboid facet; df, discoid facet; dplf, dorsoplantar foramen; ectf, ectal facet; Fibf, fibular facet; Navf, navicular facet; of, odontoid facet; stf, sustentacular facet; tc, tuber calcanei; Tibf, tibial facets (astragalar trochlea). Scale bar = 2 cm.
Figure 14 in Higher-order phylogeny of modern birds (Theropoda, Aves: Neornithes) based on comparative anatomy. II. Analysis and discussion
Figure 14. Detailed segment of strict consensus tree of all MPTs recovered in present study. Part C. Neornithes: nodes are labelled above by percentages of bootstrapped replicates in which node was retained (italics), and below by Bremer support indices (bold type).
Figure 14 in A new Thai Mesozoic lungfish (Sarcopterygii, Dipnoi) with an insight into post-Palaeozoic dipnoan evolution
Figure 14. Upper and lower tooth plates of lungfishes from various Asian Mesozoic localities referred to Ferganoceratodus. The upper row shows the plates with their actual position (right or left side) and respective size; the lower row shows the plates adjusted to a similar size and position for comparison.
Figure 14. A–D in New and little-known Komokiacea (Foraminifera) from the bathyal and abyssal Weddell Sea and adjacent areas
Figure 14. A–D, Type specimens of Normanina species. A, B, Damaged syntype of Haliphysema confertum Norman, 1878, Natural History Museum, London, reg. no. ZF3657, confocal light photographs showing entire specimen (A) and detail of tubules and terminal swellings (B); C, holotype of Normanina tylota Tendal & Hessler, Zoological Museum, Copenhagen, photographed in alcohol using combination of reflected and transmitted light; D, opposite side of same specimen, transmitted light. E, F, Normanina sp. from Stn 142#5. E, general view by reflected light; F, different view using combination of reflected and transmitted light.
Figure 14 in Anatomy, shell morphology, and microstructure of the living fossil Pulvinites exempla (Hedley, 1914) (Mollusca: Bivalvia: Pulvinitidae)
Figure 14. Details of mantle edge morphology in Pulvinites exempla (scanning electron microscopy; AMS C.129659, 62.2 mm). A, cross-section of the mantle; the arrow shows OF-2 (pallial skirt) (scale bar = 200 µm). B, lateral view of the interior mantle margin showing the outer surfaces of IF-1, IF-2, and OF-1; the arrow indicates the sinuous groove separating the inner fold (scale bar = 200 µm). C, magnified large tentacle of the inner surface of IF-1 (scale bar = 25 µm). D, small laterally compressed tentacles of the outer surface of IF-2 (scale bar = 50 µm). E, ciliated inner surface of IF-1 (scale bar = 10 µm). F, smooth inner surface of OF-1 (scale bar = 10 µm); IF, inner mantle fold; OF, outer fold; p, periostracum; t, tentacle.
Figure 14 in A revision of the genus Paraprionospio Caullery (Polychaeta: Spionidae)
Figure 14. Paraprionospio patiens sp. nov., holotype. A, anterior end, in dorso-lateral view; B, palp; C, 1st lamella from the base of right branchia on setiger 1 in cross-section, seen from top; D, 3rd lamella of the same branchia in cross-section, seen from top; E, lamella in middle region of the same branchia in cross-section, seen from top; F, distal end of the same branchia, seen from the side; G, setigers 20–23; H, posterior end, in ventral view.
Figure 14 in The interrelationships of Devonian lungfishes (Sarcopterygii: Dipnoi) as inferred from neurocranial evidence and new data from the genus Soederberghia Lehman, 1959
Figure 14. Reinterpretation of the neurocranium of Griphognathus minutidens. Anterior is to the top. A, photograph of NRM P6173, showing otic and occipital regions in ventral view; B, interpretive drawing (modified from Schultze, 1969). Shaded area in B indicates portions of the otic and occipital region underlain by the missing portions of the parasphenoid stalk and corpus, while diagonal hatching indicates damaged bone surface. The apparent foramina on the wall of the otic capsule have been interpreted as accommodating cranial nerves by Schultze (1969), but this specimen is badly crushed and uncertainties about these identifications are indicated by appending them with '?'. The unossified facet for the first epibranchial was initially mistaken as a foramen for a ventral branch of the acoustic (VIII) nerve (Schultze, 1969). Scale bar represents 10 mm.
Figure 14 in Palaeoheterodont diversity (Mollusca: Trigonioida + Unionoida): what we know and what we wish we knew about freshwater mussel evolution
Figure 14. Representatives of the Etheriidae. A, Etheria elliptica MCZ 293466. B, Acostaea rivolii UMMZ 23485. C, Pseudomulleria dalyi UMMZ 112658.
Figure 14 in A new species of Dyrosaurus (Crocodylomorpha, Dyrosauridae) from the early Eocene of Morocco: phylogenetic implications
Figure 14. Right scapula and coracoid of Dyrosaurus maghribensis sp. nov., OCP DEK-GE 254, Ypresian of Mera el Arech, Oulad Abdoun Basin, Morocco: A, lateral view; B, lateroventral view; C, interpretative drawing of (A) and (B).
Figure 14 in A new genus from the continental slope off Brazil and the discovery of the first males in the Hirsutiidae (Crustacea: Peracarida: Bochusacea)
Figure 14. Montucaris distincta gen. et sp. nov., brooding female. A, paragnaths with most integumental ornamentation omitted, anterior (a, b: processes on posterior surface labelled as in Fig. 3); B, detail of right paragnath, anterior (c: striated sclerotized plate along inner margin of bilobed process); C, right first pereopod, lateral; D, detail of dactylus with setae omitted. Scale bars: 0.25 mm (C, D); 0.125 mm (A); 0.05 mm (B).
Figure 14 in Bone surface texture as an ontogenetic indicator in long bones of the Canada goose Branta canadensis (Anseriformes: Anatidae)
Figure 14. Irregular resorptive surface with large erosion bays lined by numerous osteoclasts (arrows), seen in transverse section (DMNH 83592, tibiotarsus section a). P, periosteum. Scale bar = 92 µm.
Figure 14. Evansula arenicola Nicholls, 1939. A in Revision of the genus Evansula T. Scott, 1906 (Copepoda, Harpacticoida, Cylindropsyllidae) with a description of three new species
Figure 14. Evansula arenicola Nicholls, 1939. A, female urosome (excluding P5-bearing somite), ventral; B, male urosome (excluding P5-bearing somite), ventral; C, male urosome (excluding P5-bearing somite), lateral; D, female genital field, ventral; E, maxilliped, posterior (inset showing syncoxal seta in anterior view).
Figure 14 in Killer sperm whale: a new basal physeteroid (Mammalia, Cetacea) from the Late Miocene of Italy
Figure 14. Hypothetical reconstructions of Zygophyseter varolai gen. et sp. nov. A, head in lateral view with a parasagittal section of the nasal area based on Physeter macrocephalus (Heyning, 1989: 36); B, head in dorsal view with evidence for the circular supracranial basin of the skull; C, body in lateral view.
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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.