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Figure 9 in Comparative morphology of the dermal palate in squamate reptiles, with comments on phylogenetic implications
Figure 9. Three-dimensional high-resolution X-ray computed tomographic (HRXCT) reconstructions. A, Heloderma horridum (Wiegmann, 1829), ventral view; B, H. horridum, sagittal cutaway slice 160; C, Lanthanotus borneensis, ventral view; D, L. borneensis, transverse cutaway slice 067. Scale bars = 5 mm.
Figure 6 in Comparative morphology of the dermal palate in squamate reptiles, with comments on phylogenetic implications
Figure 6. Three-dimensional high-resolution X-ray computed tomographic (HRXCT) reconstructions. A, Lacerta viridis (Laurenti, 1768), ventral view; B, L. viridis, transverse cutaway slice 066; C, L. viridis, sagittal cutaway slice 173; D, L. viridis, transverse cutaway slice 087; E, Cordylus mossambicus (Fitzsimons, 1958), transverse cutaway slice 107. Scale bars = 5 mm.
Figure 7 in Comparative morphology of the dermal palate in squamate reptiles, with comments on phylogenetic implications
Figure 7. Three-dimensional high-resolution X-ray computed tomographic (HRXCT) reconstructions of Ophisaurus apodus. A, ventral view; B, sagittal cutaway slice 161; C, transverse cutaway slice 091. Scale bar = 5 mm.
Figure 6 in A new species of Prosansanosmilus: implications for the systematic relationships of the family Barbourofelidae new rank (Carnivora, Mammalia)
Figure 6. Auditory region of Nimravidae, Barbourofelidae and Felidae. A, auditory region in juvenile Dinictis (UNSM 4051–81) from Nebraska (Hunt, 1987: fig. 5A). B, auditory bulla of Barbourofelis lovei (UF 55859) from Love bone bed, Florida (Hunt, 1987: fig. 9B). C, auditory bulla of Lynx rufus (UNSM 33–67) from Nebraska (Hunt, 1987: fig. 10B). D, auditory region of Sansanosmilus palmidens (MNHN Sa 3384) from Sansan, France. Abbreviations after Hunt (1987). E, ossified caudal entotympanic - Ea, anterior lamina, Ep, posterior lamina, Ev, vertical lamina; P, petrosal; PS, nimravid proseptum; Rs, septate lateral margin of rostral entotympanic; SB, septum bullae; SQ, squamosal; T, ectotympanic.
Figure 4 in A new species of Prosansanosmilus: implications for the systematic relationships of the family Barbourofelidae new rank (Carnivora, Mammalia)
Figure 4. One of eight most parsimonious trees obtained from the cladistic analysis. See text for discussion and Table 3 for character support.
Figure 7 in Implications of the mastoid anatomy of larger extant felids for the evolution and predatory behaviour of sabretoothed cats (Mammalia, Carnivora, Felidae)
Figure 7. Drawing of the skull and anterior cervicals of Panthera tigris (top) and Homotherium latidens (bottom) with fibres of selected muscles. Muscle numbering as in Figs 1–5. A black circle in the condylar area represents the position of the rotation centre of the atlanto-occipital articulation. Notice how, in Homotherium, most fibres of the obliquus capitis cranialis extend well below that centre of rotation, and would therefore have a stronger head-flexing action. Notice also how the greater distance between the posterior tip of the atlas wings and the tip of the mastoid process in Homotherium makes for longer inferior fibres of the obliquus capitis cranialis muscle.
Figure 6 in Implications of the mastoid anatomy of larger extant felids for the evolution and predatory behaviour of sabretoothed cats (Mammalia, Carnivora, Felidae)
Figure 6. Photographs of the mastoid region of skull in female lion, Panthera leo (top) and scimitar-toothed cat, Homotherium latidens (bottom) from Incarcal, Spain (IN-I 929). Note that the back of the skull is broken in the fossil. Muscle insertion areas are marked; muscle numbering as in Figs 1–5. M, mastoid process; P, paroccipital process.
Figure 5 in Implications of the mastoid anatomy of larger extant felids for the evolution and predatory behaviour of sabretoothed cats (Mammalia, Carnivora, Felidae)
Figure 5. (A) Photograph and schematic representation of deep muscles of the neck in a lioness. The posterior portion of the temporalis muscle has been removed to make visible the nuchal region of skull and neck muscles attaching to it. 7, deep extensors of the neck, including rectus capitis dorsalis major and minor; Am, auditory meatus; Mp, mastoid process; Nc, nuchal crest. (B) Photograph and schematic representation of deep muscles of the neck of a male puma in ventral view. 9, m. rectus capitis lateralis.
Figure 4 in Implications of the mastoid anatomy of larger extant felids for the evolution and predatory behaviour of sabretoothed cats (Mammalia, Carnivora, Felidae)
Figure 4. (A) Photograph and schematic representation of deep muscles of the neck in male tiger. 5, m. obliquus capitis caudalis; 6, m. obliquus capitis cranialis; 8, m. digastricus; At, lateral border of the atlas wings; Ax, dorsal border of axis. (B) Photograph and schematic representation of deep muscles in a male puma. f, additional superficial fibres of m. obliquus capitis cranialis, dorsal to the atlas wing.
Figure 2 in Implications of the mastoid anatomy of larger extant felids for the evolution and predatory behaviour of sabretoothed cats (Mammalia, Carnivora, Felidae)
Figure 2. Photograph and schematic representation of superficial layer of head and neck muscles of male puma. 1, m. brachiocephalicus.
Figure 1 in Implications of the mastoid anatomy of larger extant felids for the evolution and predatory behaviour of sabretoothed cats (Mammalia, Carnivora, Felidae)
Figure 1. Schematic drawing of the skull and cervical vertebrae of the scimitar-toothed cat Homotherium latidens showing the hypothetical motions of the stabbing bite (top) and the canine shear bite (bottom). In the first case the main rotation is around a point behind the thoraco-cervical joint (white circle) and the posterior cervicals, whereas in the second case, the main rotation occurs at the atlantooccipital joint (white circle). In the stabbing model (top), the pull of the brachiocephalic muscles (single headed arrow) and of the scalenes (two headed arrow) provides the main force for the strike. In the canine shear-bite model (bottom), the pull of the atlanto-mastoid muscles (short two-headed arrow) is the most important force for the penetration of the upper canines.
Figure 5 in The ossified Meckel's cartilage and internal groove in Mesozoic mammaliaforms: implications to origin of the definitive mammalian middle ear
Figure 5. (A) The skull of Zhangheotherium (IVPP V7466). 1, Meckelian groove; 2, ossified Meckel's cartilage; 3, a hyoid element. (B) Medial view of the left mandible with partial ossified Meckel's cartilage of Gobiconodon (IVPP V12585).
Figure 1 in The ossified Meckel's cartilage and internal groove in Mesozoic mammaliaforms: implications to origin of the definitive mammalian middle ear
Figure 1. The right mandible and ossified Meckel's cartilage (OMC) of Repenomamus (holotype, IVPP V12549). (A & B) Medial views of the mandible with the OMC being removed in (A); (C) dorsomedial view; (D) ventral view; (E) radiographic image of the mandible; (F) a hyoid element from IVPP V12728. Modified from Wang et al. (2001).
Figure 4 in The ossified Meckel's cartilage and internal groove in Mesozoic mammaliaforms: implications to origin of the definitive mammalian middle ear
Figure 4. Ossified Meckel's cartilages (OMC) of Repenomamus. (A–D) Ventral, lateral, dorsal, and medial views of the OMC in IVPP V12549; (E–H) the same views of the OMC in IVPP V12728.
Figure 3. FSP-ITD 342 in Juvenile cranial anatomy of Nimravidae (Mammalia, Carnivora): biological and phylogenetic implications
Figure 3. FSP-ITD 342, cranium. Stereophotographs of the ventral side the right auditory region. Abbreviations: BO, basioccipital; CF, cochlear fenestra; CT, crista tympanica; EC, ectotympanic with anterior and posterior crura; EO, exoccipital; ET, fragment of caudal entotympanic; FO, foramen ovale; GF, glenoid fossa; MP, mastoid process, PLEP, posterolateral extension of the petrosal; PN, petrosal notch separating the main part of the posterolateral extension from the promontorium; POAC, posterior opening of the alisphenoid canal; PP, petrosal promontorium; SQ, squamosal; TH, dorsal fragment of the tympanohyal. Solid circles indicate the area of attachment for brachio- and/or sternocephalicus; the solid triangle indicates the small depression posteromedially to the mastoid.
Figure 18 in A multivariate analysis of the fringe-toed lizards of the Acanthodactylus scutellatus group (Squamata: Lacertidae): systematic and biogeographical implications
Figure 18. Geographical distribution of Acanthodactylus dumerili. Dotted lines indicate the approximate limits of the distribution of Acanthodactylus scutellatus in the Sahara. Data from Salvador (1982), Bons & Geniez (1996), Nouïra (1996), this study.
Figure 16 in A multivariate analysis of the fringe-toed lizards of the Acanthodactylus scutellatus group (Squamata: Lacertidae): systematic and biogeographical implications
Figure 16. (a) Acanthodactylus scutellatus audouini, male, paralectotype of Acanthodactylus scutellatus var. audouini, BMNH 97.10.28.316, Wadi Halfa (Egypt), close-up of dorsal scales. (b) A. senegalensis, male, EPHE Mch1, coast north of Dakar (Senegal), close-up of dorsal scales. (c) A. dumerili, male, MNHN 1997.3764, Blaouakh (Mauritania), close-up of dorsal scales. (d) A. longipes, male, EPHE AF4, Akreïdil, 50 km NE of Nouakchott (Mauritania), close-up of dorsal scales.
Figure 15 in A multivariate analysis of the fringe-toed lizards of the Acanthodactylus scutellatus group (Squamata: Lacertidae): systematic and biogeographical implications
Figure 15. Snout-vent length of females in our samples of continental Sahara Acanthodactylus dumerili and A. scutellatus audouini.
Figure 19 in A multivariate analysis of the fringe-toed lizards of the Acanthodactylus scutellatus group (Squamata: Lacertidae): systematic and biogeographical implications
Figure 19. Geographical distribution of Acanthodactylus longipes. Data from Salvador (1982), Baha El Din (1994), Bons & Geniez (1996), Nouïra (1996), this study.
Figure 10 in A multivariate analysis of the fringe-toed lizards of the Acanthodactylus scutellatus group (Squamata: Lacertidae): systematic and biogeographical implications
Figure 10. Bivariate plot of PC3 and PC4 scores generated by a PCA run on all adult specimens of Acanthodactylus aureus and A. taghitensis (males and females together) using the same 12 variables as in the other PCAs.
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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.