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76 results for “myology”
Fig. 8 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 8. Ventral view of chest muscles of Parascalops; superficial muscles on left, deeper muscles on right.
Fig. 21 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 21. Present continental distributions mapped on most parsimonious cladogram. Distributions from Corbet and Hill (1991).
Fig. 5 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 5. Lateral view of snout muscles of Parascalops. A, Superficial layer; B, middle layer; C, deep layer.
Fig. 18 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 18. Medial view of lower leg muscles of Parascalops. A, Superficial muscles; B, deeper muscles.
Fig. 17 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 17. Lateral view of lower leg muscles of Parascalops. A, Superficial muscles; B, deeper muscles.
Fig. 16 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 16. Medial view of pelvic limb muscles of Parascalops, M. gracilis removed.
Fig. 13 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 13. Intrinsic muscles of the manus of Galemys.
Fig. 9 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 9. Dorsal view of pectoral limb muscles of Parascalops.
Fig. 10 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 10. Ventral view of pectoral limb muscles of Parascalops.
Fig. 2 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 2. Masticatory muscles of Parascalops.
Fig. 12 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 12. Ventral view of forearm muscles of Parascalops.
Fig. 15 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 15. Lateral view of pelvic limb muscles of Parascalops, superficial muscles removed.
Fig. 11 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 11. Dorsal view of forearm muscles of Parascalops. A, Superficial muscles; B, deeper muscles.
Fig. 7 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 7. Lateral view of neck muscles of Parascalops.
Fig. 19 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 19. Intrinsic muscles of the pes of Neurotrichus.
Fig. 4 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 4. Lateral view of facial muscles of Parascalops, M. sphincter colli superficialis removed.
Fig. 14 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 14. Lateral view of pelvic limb muscles of Parascalops.
Data from: Comparative cranial myology and biomechanics of Plateosaurus and Camarasaurus and evolution of the sauropod feeding apparatus
Sauropodomorpha represents an important group of Mesozoic megaherbivores, and includes the largest terrestrial animals ever known. It was the first dinosaur group to become abundant and widespread, and its members formed a significant component of terrestrial ecosystems from the Late Triassic until the end of the Cretaceous. Both of these factors have been explained by their adoption of herbivory, but understanding the evolution of sauropodomorph feeding has been hampered by the scarcity of biomechanical studies. To address this, the jaw adductor musculature of the basal sauropodomorph Plateosaurus and the sauropod Camarasaurus have been reconstructed. These reconstructions provide boundary conditions for finite element models to assess differences in structural performance between the two taxa. Results demonstrate that Camarasaurus was capable of much greater bite forces than Plateosaurus, due to greater relative adductor muscle mass and shape changes to the mandible. The skull and mandible of Camarasaurus are also 'stronger' under static biting. The Plateosaurus mandible appears to compromise structural efficiency and force transmission in order to maintain relatively high jaw closure speed. This supports suggestions of facultative omnivory in basal sauropodomorph taxa. The expanded mandibular symphysis and 'lateral plates' of sauropods each lead to greater overall craniomandibular robustness, and may have been especially important in accommodating forces related to asymmetric loading. The functional roles of these characters, and observed general shape changes in increasing skull robustness, are consistent with hypotheses linking bulk-herbivory with the origin of Sauropoda and the evolution of gigantism.
Figure 1 in Hind limb myology of the common hippopotamus, Hippopotamus amphibius (Artiodactyla: Hippopotamidae)
Figure 1. Common hippo hind limb in lateral view. Asterisk (*) indicates the location of the patella deep to the fibres of the tensor fasciae latae.
Figure 8 in Hind limb myology of the common hippopotamus, Hippopotamus amphibius (Artiodactyla: Hippopotamidae)
Figure 8. Lateral view of hind foot skeleton in the ox, common hippo and pig. The hippo has four weight-bearing digits, whereas pigs and ruminants have reduced lateral digits.
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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.