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68 results for “Scapula”
Biplane fluoroscopy derived humerus and scapula kinematics during arm elevation and rotation
<p>This dataset contains torso, scapula, and humerus kinematics from 20 healthy subjects performing coronal plane abduction, scapular plane abduction, forward elevation, internal external rotation at 90º of abduction, and internal external rotation in adduction. The humerus and scapula were imaged at 100 Hz using a biplane fluoroscopy system. 3D models of the humerus and scapula were constructed from each subject’s CT scan. Model-based markerless tracking ascertained the 3D position and orientation of each bone model by semi-automatically aligning digitally reconstructed radiographs against each frame of the biplane fluoroscopy recordings. The kinematics of the torso were measured using skin marker motion capture.</p>
Fig. 1. D. emryi scapula, SNMZ 14537 in First Record Of Postcranial Bones In Devinophoca Emryi (Carnivora, Phocidae, Devinophocinae)
Fig. 1. D. emryi scapula, SNMZ 14537 (R., incomplete) in: A — anterior; B — posterior; C — lateral views.
Fig. 7 in A geometric morphometric study of sex differences in the scapula, humerus and ulna of Chaetophractus villosus (Xenarthra, Dasypodidae)
Fig. 7. Ulna. Distribution of males (black dots) and females (white dots) of Chaetophractus villosus (Desmarest, 1804) in the plane determined by the first two relative warps (RW1 and RW2). Numbers indicate specimens. Deformation grids below the graph show shape changes linked to negative (left) and positive (right) scores in RW1. Grids on the right show deformations linked to negative (below) and positive (above) scores in RW2.
Fig. 6 in A geometric morphometric study of sex differences in the scapula, humerus and ulna of Chaetophractus villosus (Xenarthra, Dasypodidae)
Fig. 6. Scatterplot for the ulna of Chaetophractus villosus (Desmarest, 1804), showing the distribution of the individuals in the plane formed by the two first principal components. The black outlines below the plot represent the shape variation associated to PC1, and those of the right show the changes associated to PC2 with respect to the consensus of the species (grey outlines).
Fig. 4 in A geometric morphometric study of sex differences in the scapula, humerus and ulna of Chaetophractus villosus (Xenarthra, Dasypodidae)
Fig. 4. Humerus. Distribution of males (black dots) and females (white dots) of Chaetophractus villosus (Desmarest, 1804) in the plane determined by the first two relative warps (RW1 and RW2). Numbers indicate specimens. Deformation grids below the graph show shape changes linked to negative (left) and positive (right) scores in RW1. Grids on the right show deformations linked to negative (below) and positive (above) scores in RW2.
Fig. 3 in A geometric morphometric study of sex differences in the scapula, humerus and ulna of Chaetophractus villosus (Xenarthra, Dasypodidae)
Fig. 3. Scatterplot for the humerus of Chaetophractus villosus (Desmarest, 1804), showing the distribution of the individuals in the plane formed by the two first principal components. The black outlines below the plot represent the shape variation associated to PC1, and those of the right show the changes associated to PC2 with respect to the consensus of the species (grey outlines).
Fig. 2 in A geometric morphometric study of sex differences in the scapula, humerus and ulna of Chaetophractus villosus (Xenarthra, Dasypodidae)
Fig. 2. Canonical analysis for the humerus of males and females of Chaetophractus villosus (Desmarest, 1804). The bone outlines below the graph represent the tendencies to deformation in males and females (black dots and lines) with respect to the consensus of the species (grey dots and lines) along the axis.
Fig. 1 in A geometric morphometric study of sex differences in the scapula, humerus and ulna of Chaetophractus villosus (Xenarthra, Dasypodidae)
Fig. 1. Landmarks digitised on the left appendicular bones of Chaetophractus villosus (Desmarest, 1804). Scapula in dorsal view; humerus in caudal view; ulna in lateral view.
Fig. 5 in A geometric morphometric study of sex differences in the scapula, humerus and ulna of Chaetophractus villosus (Xenarthra, Dasypodidae)
Fig. 5. Canonical analysis for the ulna of males and females of Chaetophractus villosus (Desmarest, 1804). The bone outlines below the graph represent extreme individuals (black dots and lines) with respect to the consensus of the species (grey dots and lines) along the axis.
Fig. 8 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids
Fig. 8. Morphological features distinguishing the distal portion of the humerus of Rangifer tarandus (A) and Cervus elaphus (B), in anterior (A1, B1), distal (A2,B2), and posterior (A3,B3) views (modified from Breda 2005).
Fig. 7 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids
Fig. 7. Morphological features distinguishing the proximal portion of the humerus of Rangifer tarandus (A) and Cervus elaphus (B) (modified from Pales and García 1981).
Fig. 6 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids
Fig. 6. Scatterplots of different combinations of scapular measurements and indices for Rangifer tarandus and Cervus elaphus from Kiputz IX (southern Pyrenees, Spain), Late Pleistocene. Abbreviations: GLP, greatest anteroposterior length of the glenoid process; LG, greatest anteroposterior length of the glenoid cavity; SLC, minimum diameter of the scapular neck.
Fig. 3 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids
Fig. 3. Osteological measurements of the scapula (A, B) and the humerus (C, D) (modified from Weinstock 2000a). All drawings are based on Rangifer tarandus.
Fig. 4 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids
Fig. 4. Morphological features distinguishing the scapulae of the cervid mammals Rangifer tarandus, BGG KI-IX.2D.39.618 (A) and Cervus elaphus, BGG KI-IX.2C.28.142 (B), from Kiputz IX (southern Pyrenees, Spain), Late Pleistocene, in lateral (A 1, B 1) and distal (A 2, B 2) views; α, the angle formed by the glenoid cavity and the supraglenoid tubercle.
Fig. 9 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids
Fig. 9. Scatterplot of the greatest breadth of the trochlea (BT) vs. the depth of the distal epiphysis (Dd) of the humerus of Rangifer tarandus and Cervus elaphus from Kiputz IX and other European sites.
Text-fig. 3. Right scapula of the large Staniantsi-beaver in caudo-lateral and distal view with markings of the anatomical terms used for the description of the scapula. Left figure: caudal view of GPIT/MA/09858-9. Right figure: mirrored distal view of GPIT/MA/03819. in Castor-Like Postcranial Adaptation In An Uppermost Miocene Beaver From The Staniantsi Basin (Nw Bulgaria)
Text-fig. 3. Right scapula of the large Staniantsi-beaver in caudo-lateral and distal view with markings of the anatomical terms used for the description of the scapula. Left figure: caudal view of GPIT/MA/09858-9. Right figure: mirrored distal view of GPIT/MA/03819.
FIG. 41. — Bretskya scapula n. gen., n in Diversity of chemosymbiotic bivalves on coral reefs: Lucinidae (Mollusca, Bivalvia) of New Caledonia and Lifou
FIG. 41. — Bretskya scapula n. gen., n. sp., Pandanan Island, Philippines:A, dorsal view of paratype (BMNH 20050580); B, protoconch; C, detail of sculpture. Scale bars: A, 1 mm; B, 50 µm; C, 100 µm.
FIG. 40. — Bretskya scapula n. gen., n in Diversity of chemosymbiotic bivalves on coral reefs: Lucinidae (Mollusca, Bivalvia) of New Caledonia and Lifou
FIG. 40. — Bretskya scapula n. gen., n. sp.: A-J, Pandanan Island, Philippines; A-C, holotype (BMNH 20050579), exterior of right valve and interior of right and left valves; D-J, paratype (BMNH 20050580); D-F, exterior of right valve and interior of right and left valves; G, exterior of right valve; H, exterior of right valve; I, J, detail of hinges of left and right valves; K, L, Philippines, MUSORSTOM 3, stn DR 140, 93-99 m (MNHN); M, N, Touho, stn 1249, New Caledonia, exterior and interior right valve. Scale bars: A-H, K-N, 2.0 mm; I, J, 1.0 mm.
Text-fig. 6. Disarticulation marks on humerus 98-594-C-P (2) for disarticulation from the scapula, for the metrics of this bone see Table 12. in Consumption Of Canid Meat At The Gravettian Předmostí Site, The Czech Republic
Text-fig. 6. Disarticulation marks on humerus 98-594-C-P (2) for disarticulation from the scapula, for the metrics of this bone see Table 12.
Left Scapula
Human left scapula from the anthropology department's collections at University of North Carolina at Greensboro, modeled with the permission of Dr. Robert Anemone. Creator: Cory Henderson, undergraduate Anthropology and Biology student at University of North Carolina at Greensboro. Hardware: NextEngine Desktop 3D Scanner, Model 2020i Software: ScanStudioHD and RapidWorks Source: Objaverse 1.0 / Sketchfab
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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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.