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Figure 18 in Functional anatomy and biomechanics of the postcranial skeleton of Simocyon batalleri (Viret, 1929) (Carnivora, Ailuridae) from the Late Miocene of Spain
Figure 18. Dorsal views of articulated left calcaneus and astragalus of Ailuropoda melanoleuca (A), Ailurus fulgens (B), Simocyon batalleri from Batallones-1 (C), Gulo gulo (D) and Potos flavus (E).
Figure 17 in Functional anatomy and biomechanics of the postcranial skeleton of Simocyon batalleri (Viret, 1929) (Carnivora, Ailuridae) from the Late Miocene of Spain
Figure 17. Medial view of the right radius of Simocyon batalleri from batallones-1 (A), Gulo gulo (B) and Potos flavus (C) showing the proximal torsion observed in S. batalleri and P. flavus. The bones are illustrated at the same size.
Figure 38. Caudal skeleton. A in Comparative osteology and phylogenetic systematics of fossil and living bony-tongue fishes (Actinopterygii, Teleostei, Osteoglossomorpha)
Figure 38. Caudal skeleton. A, †Phareodus testis (UMA F11332, 260 mm SL). B, Osteoglossum bicirrhosum (FMNH 109232a, 270 mm SL). C, Pantodon buchholzi (FMNH 63752, 62 mm SL). D, Heterotis niloticus (UMA F10653, 75 mm SL). Anterior facing left.
Figure 37. Caudal skeleton. A in Comparative osteology and phylogenetic systematics of fossil and living bony-tongue fishes (Actinopterygii, Teleostei, Osteoglossomorpha)
Figure 37. Caudal skeleton. A, Hiodon tergisus (TU 108166 A, 52 mm SL). B, †Lycoptera davidi (UMA F11260a, 75 mm SL). C, Petrocephalus simus (MCZ 50113, 55 mm SL). D, Chitala sp. (UMA F10341, 75 mm SL). Anterior facing left. Illustration of Hiodon modified from Hilton (2002: fig. 74D). Illustration of †Lycoptera is of right side and image reversed so anterior facing left.
Figure 13 in The cranial skeleton of the Early Permian aquatic reptile Mesosaurus tenuidens: implications for relationships and palaeobiology
Figure 13. Cladogram illustrating relationships of mesosaurs based on a PAUP analysis of a modified version of the data matrix in Laurin & Reisz (1995), with additional characters from Modesto (1999b). See text for discussion. Tree length = 328, consistency index (excluding uninformative characters) = 0.66, rescaled consistency index = 0.41.
Figure 10 in The cranial skeleton of the Early Permian aquatic reptile Mesosaurus tenuidens: implications for relationships and palaeobiology
Figure 10. Mesosaurus tenuidens, SAM PK-K8381 (part and counterpart). Palate, braincase, mandible and anteriormost cervical vertebrae in (A) dorsal and (B) ventral views.
Figure 12. Mesosaurus tenuidens, MCZ 3373 in The cranial skeleton of the Early Permian aquatic reptile Mesosaurus tenuidens: implications for relationships and palaeobiology
Figure 12. Mesosaurus tenuidens, MCZ 3373 (in part). Skull roof, mandible, and cervical vertebrae 2–6 in dorsal view.
Figure 9. Mesosaurus tenuidens, SMNH R212 in The cranial skeleton of the Early Permian aquatic reptile Mesosaurus tenuidens: implications for relationships and palaeobiology
Figure 9. Mesosaurus tenuidens, SMNH R212. Palate, braincase, hyoid element, mandible and anteriormost cervicals in ventral view.
Figure 4 in The cranial skeleton of the Early Permian aquatic reptile Mesosaurus tenuidens: implications for relationships and palaeobiology
Figure 4. Mesosaurus tenuidens, part and counterpart. A, SMNH R208. Skull, mandible and anterior cervical vertebrae in left lateral view. B, SMNH R207a. Skull, mandible and anterior cervical vertebrae in right lateral view. Arabic numerals denote presacral vertebrae in this and subsequent figures.
Figure 5. Mesosaurus tenuidens, MCZ 4028 in The cranial skeleton of the Early Permian aquatic reptile Mesosaurus tenuidens: implications for relationships and palaeobiology
Figure 5. Mesosaurus tenuidens, MCZ 4028, part and counterpart. Left lateral view of skull, mandible and anteriormost cervical vertebrae (MCZ 4028b) above, with counterpart of snout and partial mandible in medial view, with associated vomer (MCZ 4028a) below.
Figure 7. Mesosaurus tenuidens, MCZ 4031a in The cranial skeleton of the Early Permian aquatic reptile Mesosaurus tenuidens: implications for relationships and palaeobiology
Figure 7. Mesosaurus tenuidens, MCZ 4031a. Skull, mandible, and cervical vertebrae in left lateral view, and dorsal vertebrae and ribs in right lateral view.
Figure 2 in The cranial skeleton of the Early Permian aquatic reptile Mesosaurus tenuidens: implications for relationships and palaeobiology
Figure 2. Reconstruction of the skull of Mesosaurus tenuidens in occipital view. The regular stipple pattern represents a hypothetical cartilaginous bridge between the skull roof and the braincase.
Figure 11 in Aspects of the functional morphology in the cranial and cervical skeleton of the sabre-toothed cat Paramachairodus ogygia (Kaup, 1832) (Felidae, Machairodontinae) from the Late Miocene of Spain: implications for the origins of the machairodont killing bite
Figure 11. Comparative views of the skull and mandible of (A) Neofelis nebulosa, and (B) Paramachairodus ogygia (artwork by M. Antón).
Figure 10 in Aspects of the functional morphology in the cranial and cervical skeleton of the sabre-toothed cat Paramachairodus ogygia (Kaup, 1832) (Felidae, Machairodontinae) from the Late Miocene of Spain: implications for the origins of the machairodont killing bite
Figure 10. Photographs of the first to seventh cervical vertebrae (C1-C7) (anterior to left) in Fig. 9, in lateral view. A, Paramachairodus ogygia from Batallones-1. B, Panthera pardus.
Figure 13 in Comparative osteology of the Danio (Cyprinidae: Ostariophysi) axial skeleton with comments on Danio relationships based on molecules and morphology
Figure 13. Comparison of phylogenies derived from morphological and combined data sets. A, Strict consensus for molecular data (581 steps; CI = 0.801); B, Strict consensus tree for combined morphological and molecular data sets (611 steps, CI = 0.861). Bootstrap values are given above each internode. Note that the relationships within the slender-bodied clade are identical in the two trees, but relationships within the deep-bodied clade differ in the two trees.
Figure 12 in Comparative osteology of the Danio (Cyprinidae: Ostariophysi) axial skeleton with comments on Danio relationships based on molecules and morphology
Figure 12. Phylogeny of Danio according to morphological data. This phylogeny is the strict consensus tree derived from 16 morphological characters (20 steps, CI = 0.90). Character support for each node is given along side each branch. Numbers refer to characters listed in Table 2.
Figure 9 in Comparative osteology of the Danio (Cyprinidae: Ostariophysi) axial skeleton with comments on Danio relationships based on molecules and morphology
Figure 9. Separation of the epural from the neural arch. A, Opsariichthys (MCZ 32375) in which the epural abuts the rudimentary neural arch (arrow); B, D. pulcher (CU 77840) illustrates the separation of the neural arch and epural found in all Danio examined. Scale bars = 1 mm.
Figure 10 in Comparative osteology of the Danio (Cyprinidae: Ostariophysi) axial skeleton with comments on Danio relationships based on molecules and morphology
Figure 10. Late ontogenetic variation in the posterior process of the fifth vertebra of D. kerri. A, a 'young' individual (CU 82554) of standard length (SL) = 27.6 mm; This individual is known to be less than five years old as it was an F1 from parents wild-caught in 1995. B, a larger individual (SL = 38.7 mm, CU 82551) and C, even larger individual (SL = 43.3 mm, CU 82551). B and C are known to be more than 5 years old; they were caught as adults in 1995 and maintained in captivity for 5 years. Scale bar = 0.5 mm.
Figure 11 in Comparative osteology of the Danio (Cyprinidae: Ostariophysi) axial skeleton with comments on Danio relationships based on molecules and morphology
Figure 11. Intraspecific variation of the scaphium in D. kerri. A, 'young' individual of standard length (SL) = 27.6 mm (CU 82554); This individual is known to be less than five years old as it was an F1 from parents wild-caught in 1995. B, larger individual (SL = 38.7 mm, CU 82551); C, an even larger individual (SL = 43.3 mm, CU 82551). B and C are known to be more than 5 years old; they were caught as adults in 1995 and maintained in captivity for 5 years. Scale bar = 0.5 mm.
Figure 8 in Comparative osteology of the Danio (Cyprinidae: Ostariophysi) axial skeleton with comments on Danio relationships based on molecules and morphology
Figure 8. Variation in the caudal skeleton of Danio. A, D. aequipinnatus (AMNH 15761); B, D. albolineatus (CU 77841); C, D. devario (CU 82548); D, D. kerri (CU 82554) note absence of the sixth hypural; E, D. malabaricus (MCZ 52399) note doubling of neural spines (arrow 1) and presence of the sixth hypural; F, D. pathirana (CU 85509); G, D. pulcher (CU 77840); H, D. quangbinhensis (AMNH 227913); I, D. regina (CU 82550); J, D. rerio (CU 82546); K, D. browni (CU 82553). Scale bars = 1 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)
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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.