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4,028 results for “Mammalia”
FIGURA 11 in Morcegos Do Estado Do Paraná, Brasil (Mammalia, Chiroptera): Riqueza De Espécies, Distribuição E Síntese Do Conhecimento Atual M M Abstract
FIGURA 11. Registros de ocorrência de: A) C. doriae (O), C. villosum (Q) e S. tildae (V); B) P. lineatus, no Estado do Paraná.
FIGURA 23 in Morcegos Do Estado Do Paraná, Brasil (Mammalia, Chiroptera): Riqueza De Espécies, Distribuição E Síntese Do Conhecimento Atual M M Abstract
FIGURA 23. Distribuição das localidades com registros de quirópteros no Estado do Paraná. As informações geográficas de cada ponto podem ser encontradas no anexo A.
Fig. 8 in Basicranial Anatomy of the Living Linsangs Prionodon and Poiana (Mammalia, Carnivora, Viverridae), with Comments on the Early Evolution of Aeluroid Carnivorans
Fig. 8. Rostral entotympanic fused to the inner margin of the ectotympanic in Prionodon (AMNH 163595), medial view, ventral at top. Dashed line indicates path of the internal carotid artery within the ventral edge of the rostral entotympanic.
Fig. 7 in Basicranial Anatomy of the Living Linsangs Prionodon and Poiana (Mammalia, Carnivora, Viverridae), with Comments on the Early Evolution of Aeluroid Carnivorans
Fig. 7. Dissection of the auditory region of Prionodon pardicolor (AMNH 163595) in oblique lateral view. The posterior chamber of the bulla has been opened (A), revealing the inflected dorsal margin of the caudal entotympanic applied to the petrosal, and the ectotympanic resting on the promontorium anterior to the round window. Removal of the ectotympanic and rostral entotympanic (B) allows an unrestricted view of the petrosal promontorium with its robust ventral process forming an incipient flange buttressing the edge of the basioccipital. Note that the caudal entotympanic covers the ventral process of the promontorium when in place.
Fig. 4 in Basicranial Anatomy of the Living Linsangs Prionodon and Poiana (Mammalia, Carnivora, Viverridae), with Comments on the Early Evolution of Aeluroid Carnivorans
Fig. 4. The basicranium of Palaeoprionodon (MNHN Qu 9348) from Quercy: (A) ventral, (B) posteroventral, and (C) posterolateral views. In (B) small black triangles indicate line of attachment of the caudal entotympanic to the margin of the petrosal. For abbreviations in this and subsequent figures, see pages 3–4.
Fig. 11 in Small Oligocene Amphicyonids from North America (Paradaphoenus, Mammalia, Carnivora)
Fig. 11. Comparison of ontogenetic elements contributing to the auditory bulla of the small amphicyonid Paradaphoenus (left) and the canid Hesperocyon (right). T, ectotympanic; E, caudal entotympanic.
Fig. 8 in Small Oligocene Amphicyonids from North America (Paradaphoenus, Mammalia, Carnivora)
Fig. 8. Stereophotographs of the cranium (in ventral view) of the amphicyonid Cynodictis cf. longirostris, Quercy district, France (NMB Q.V. 412); M3 is absent in this individual. The basicranium preserves the anterior half of the ectotympanic bulla and the deep embayment in the lateral margin of the basioccipital, presumably for an expanded inferior petrosal venous sinus.
Fig. 3 in Small Oligocene Amphicyonids from North America (Paradaphoenus, Mammalia, Carnivora)
Fig. 3. Stereophotographs of the holotype cranium (in ventral view) of Paradaphoenus minimus (AMNH 39099), Orellan, White River Group, South Dakota. For abbreviations in this and subsequent figures, see p. 2.
Fig. 5 in Small Oligocene Amphicyonids from North America (Paradaphoenus, Mammalia, Carnivora)
Fig. 5. Stereophotographs of the maxilla (LACM 21649, Sharps Formation, South Dakota) and holotype mandible (UNSM 6002 92, lower Arikaree Group, Nebraska) of early Arikareean P. tooheyi, n. sp., known only from the central Great Plains. Note alveoli for welldeveloped M3 in maxilla.
Fig. 3 in Basicranial Anatomy of the Living Linsangs Prionodon and Poiana (Mammalia, Carnivora, Viverridae), with Comments on the Early Evolution of Aeluroid Carnivorans
Fig. 3. Skulls of the Asian linsang Prionodon pardicolor (AMNH 163595, above) and African linsang Poiana richardsoni (AMNH 51438, below) in lateral view. Figures 3–10 are stereophotographs.
Fig. 1 in Small Oligocene Amphicyonids from North America (Paradaphoenus, Mammalia, Carnivora)
Fig. 1. Geographic distribution of Paradaphoenus in North America: all fossils are from Oligocene sediments of the central Great Plains (White River and Arikaree Groups, P. minimus, P. tooheyi) and Oregon (John Day Formation, P. cuspigerus).
Fig. 2 in Small Oligocene Amphicyonids from North America (Paradaphoenus, Mammalia, Carnivora)
Fig. 2. (A) Cranium and mandibles of the genoholotype of Paradaphoenus (P. cuspigerus, AMNH 6852) from the John Day Formation, Oregon (in lateral view); (B) stereophotographs of the same individual, initially figured by Cope (1884, P1. 68, figs. 1–4) as Amphicyon cuspigerus. Scale bar in this and all subsequent figures is 1 cm in length unless otherwise noted.
Fig. 10 in Small Oligocene Amphicyonids from North America (Paradaphoenus, Mammalia, Carnivora)
Fig. 10. Stereophotographs of the basicranium of Paradaphoenus cuspigerus (AMNH 6853, referred), John Day Formation, Oregon: (A) ventral view; (B) lateral view.
Fig. 4 in Small Oligocene Amphicyonids from North America (Paradaphoenus, Mammalia, Carnivora)
Fig. 4. Mandibles of Paradaphoenus from the White River Group, western Nebraska: (A) Labial view—top, P. tooheyi, Whitneyan, UNSM 26130; middle, P. minimus, Orellan, UNSM 25305; bottom left and right, P. minimus, Orellan, UNSM 25030 and 26139. (B) Lingual view—top, P. tooheyi, UNSM 26130; middle, P. minimus, UNSM 25305; bottom left and right, P. minimus, UNSM 25030 and 26139 (stereophotographs).
Fig. 9 in Small Oligocene Amphicyonids from North America (Paradaphoenus, Mammalia, Carnivora)
Fig. 9. Stereophotographs of the basicranium of Paradaphoenus cuspigerus (AMNH 6852, holotype), John Day Formation, Oregon: (A) ventral view; (B) lateral view.
Fig. 6 in Small Oligocene Amphicyonids from North America (Paradaphoenus, Mammalia, Carnivora)
Fig. 6. Stereophotographs of the lower dentition of holotypes of Paradaphoenus tooheyi (left, UNSM 6002 92) and P. cuspigerus (right, AMNH 6852) in occlusal view. Note wider molars and more anteriorly placed m2 trigonid in AMNH 6852.
Fig. 6 in Basicranial Anatomy of the Living Linsangs Prionodon and Poiana (Mammalia, Carnivora, Viverridae), with Comments on the Early Evolution of Aeluroid Carnivorans
Fig. 6. Basicrania of Prionodon (AMNH 163595, A) and Poiana (AMNH 51438, B) in ventral view. The bony floor of the posterior chamber of the auditory bulla has been removed on one side in each individual to show the ectotympanic resting on the petrosal promontorium, and the size of the posterior chamber formed by the caudal entotympanic. Note the more expanded or inflated posterior chamber in Poiana relative to Prionodon.
Fig. 2 in Basicranial Anatomy of the Living Linsangs Prionodon and Poiana (Mammalia, Carnivora, Viverridae), with Comments on the Early Evolution of Aeluroid Carnivorans
Fig. 2. Skulls of the Quercy Palaeoprionodon (MNHN Qu 9370), the Asian linsang Prionodon pardicolor (AMNH 163595), and the African linsang Poiana richardsoni (AMNH 51438), from left to right. (A) dorsal view; (B) ventral view. Scale bar in this and all subsequent figures is 1 cm.
Fig. 10 in Basicranial Anatomy of the Living Linsangs Prionodon and Poiana (Mammalia, Carnivora, Viverridae), with Comments on the Early Evolution of Aeluroid Carnivorans
Fig. 10. Final stage of the dissection of the auditory bulla of Prionodon (AMNH 163595, A) and Poiana (AMNH 51438, B) in ventral view. Note the robust ventral process of the promontorium in Prionodon, only incipiently modified as a flange appressed against the basioccipital, hence similar to the form of the ventral process in Palaeoprionodon (compare with fig. 4). In Poiana the flange has been further modified as a thin blade and has been extended fore and aft to a greater degree than in Prionodon. The caudal entotympanic is more inflated in Poiana, broadly contacting the paroccipital process, whereas in Prionodon the caudal entotympanic is not as expanded, and the process still retains a vestige of its primitive rodlike form.
Fig. 9 in Basicranial Anatomy of the Living Linsangs Prionodon and Poiana (Mammalia, Carnivora, Viverridae), with Comments on the Early Evolution of Aeluroid Carnivorans
Fig. 9. Dissection of the auditory region of Poiana richardsoni (AMNH 51438) in oblique lateral view (compare with fig. 7). The posterior chamber of the bulla has been opened (A), showing the inflected dorsal margin of the caudal entotympanic applied to the petrosal, and the ectotympanic resting on the promontorium anterior to the round window. Removal of the ectotympanic and rostral entotympanic (B) reveals the petrosal promontorium with ventral process produced as a flange buttressing the edge of the basioccipital. The flange is more developed in Poiana than in Prionodon, and the caudal entotympanic element is more inflated.
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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.