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206 results for “humerus”
Fig. 2 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids
Fig. 2. Stratigraphic section and radiocarbon dates for the locality of Kiputz IX.
American Mastodon, humerus. Coats-Hines Site, TN
American mastodon (Mammut americanum). Left Humerus. From 1977 excavations of the Coats-Hines-Litchy site, Williamson County, TN. Source: Objaverse 1.0 / Sketchfab
Human Humerus Bone
3D model of a human humerus bone. The humerus displays irregular new bone formation resulting from Paget's disease of bone. The individual (male, 50+ years old) may have experienced impaired mobility because of the condition. From Skriðuklaustur, grave nr: 174 The physical object is stored at the National Museum of Iceland. Part of the Skriðuklaustur Monastery 1550 reconstruction. Digitisation by Open Virtual Worlds, a research team within the School of Computer Science, University of St Andrews, in cooperation with the Gunnar Gunnarsson Institute at Skriðuklaustur and the National Museum of Iceland. 3D digitisation was done by Catherine Cassidy and Iain Oliver with archaeological assistance provided by Skúli Gunnarsson. Funded by the EU Northern Periphery and Arctic Programme 2014-2020 through the "Connected Culture and Natural Heritage in a Northern Environment" (CINE) project. Source: Objaverse 1.0 / Sketchfab
Mastodon Humerus. Neath Farm, Dane Co., WI
Mastodon (*Mammut americanum*) humerus from Neath Farm locality in Dane Co., WI. UWZP 20000. Scanned in June 2022. Source: Objaverse 1.0 / Sketchfab
Evaluation of Various Methods Used to Identify the Proximal Humerus Intraosseous Vascular Access Site
ClinicalTrials.gov study NCT01742780. IPD Sharing: Not stated. Countries: 1. Publications: 3.
Comparison of Early and Late Therapy for Adults With Non-Operatively Treated Proximal Humerus Fractures
ClinicalTrials.gov study NCT00438633. IPD Sharing: Not stated. Countries: 1. Publications: 1.
IFC Therapy in Proximal Humerus Fractures
ClinicalTrials.gov study NCT04553497. IPD Sharing: NO. Countries: 1. Publications: 4.
HO Prophylaxis Therapy for Distal Humerus Fractures
ClinicalTrials.gov study NCT03724422. IPD Sharing: NO. Countries: 1. Publications: 9.
Data from: A 3D geometric morphometric analysis of the bovid distal humerus, with special reference to Rusingoryx atopocranion (Pleistocene, Eastern Africa)
Open the record for dataset details and reuse information.
Mammoth - Juvenile humerus
# SHCMS:G.10688 **Mammuthus primigenius** Left humerus of one of the juvenile Shropshire Mammoths. Found at Condover, Shropshire. Age: approx 14000 years. Length 38cm Width 17cm Depth 16cm. Imaged using an Artec spider scanner and processed using Artec studio 12. If you like this model or any others we produce we'd love to hear from you and how you've used them. Source: Objaverse 1.0 / Sketchfab
Seal humerus tool, XFP-119, Sanak Island, Alaska
Seal humerus tool, XFP-119, Sanak Island, Alaska. XFP-119-63. Likely 400-100 BCE. XFP-119 is a group of house and other depressions along the beach within the area of the Historic town of Sanak. There are at least three components dating approximately 400 BCE, 100BCE, and 1250-1410 CE. These artifacts were scanned with either a Faro Edge Arm or a Minolta Vivid 9i. Processed in Geomagic or Polyworks. 4-8 photos were used for texture in Geomagic Wrap. The Sanak Island artifacts are presented as a result of the research conducted under grants NSF 0326584, NSF 0508101, NSF 1139266, NSF 1321411. H. Maschner, Principal Investigator. Original digitizing work done at the IVL at Id. St. Univ. Subsequent processing completed at Global Digital Heritage. Fieldwork and analysis done with the permission and collaboration of the Pauloff Harbor Tribe and the Sanak Corporation. Source: Objaverse 1.0 / Sketchfab
UW2382_a - Trionychidae, Left Humerus
Period/Epoch: Ceonozoic/ Eocene Rock Formation: Bridger Formation State, County: Wyoming, Lincoln Taxonomy: Reptilia>Chelonia>Trionychidae These elements of a trionychid turtle are Eocene in age, and found in Wyoming. Trionychids are softshell turtles, with many extant members like the Chinese softshell turtle (Pelodiscus sinensis) and the Florida softshell turtle (Apalone ferox), to name a few. Softshell turtles tend to live in freshwater lakes and ponds, though some have adapted to more brackish water as well. These specimens were found alongside shells that properly identify them as belonging to the trionychid turtle group, based on how the shell bones look in cross-section. Scanned with the David SLS-2 Source: Objaverse 1.0 / Sketchfab
Hippopotamus Right Humerus
This is the right humerus of a juvenile hippopotamus (*Hippopotamus amphibius*) skeleton given to the Lapworth Museum by Russell Coope. It is notably robust, and several large muscle attachment sites provide anchors to powerful muscles that support the weight of the hippo and allow it to move at high speeds when it feels like it. This specimen was digitised by Jack Mayer Wood using photogrammetry, and is part of a collection of bones from this individual hippo that have been digitised. Source: Objaverse 1.0 / Sketchfab
Elephant Humerus
Humerus of an asian elephant *Elephas maximus* scanned using a Rapiscan-RTT110 X-Ray luggage scanner at Henry Mosely X Ray Facility. The CT scan was processed with Stradwin with medium smoothing. The scanner is capable of scanning several hundred objects an hour. This was an experimental scan to test its capabilities with large animal bones-no processing of slice artefacts has been done in this case. Elephant bone courtesy of the Anatomy department, University of Manchester Source: Objaverse 1.0 / Sketchfab
elliptical eumelanosomes in the feathers near the skull (b, c), neck (d, e), humerus (f, g), and ulna (h, i, j); and large oval and elliptical eumelanosomes in the feathers near the tibiotarsus (k, l). The subspherical phaeomelanosomes in the sheet-like soft tissue (m) appear to be less densely distributed than the melanosomes in the feathers. in A bizarre Jurassic maniraptoran theropod with preserved evidence of membranous wings
elliptical eumelanosomes in the feathers near the skull (b, c), neck (d, e), humerus (f, g), and ulna (h, i, j); and large oval and elliptical eumelanosomes in the feathers near the tibiotarsus (k, l). The subspherical phaeomelanosomes in the sheet-like soft tissue (m) appear to be less densely distributed than the melanosomes in the feathers.
Figure 8 in Eigensurface analysis, ecology, and modelling of morphological adaptation in the falconiform humerus (Falconiformes: Aves)
Figure 8. Ordination of the falconiform species for which accurate flight speed information was available (47 species) within the space of the first two canonical variates axes of 21 eigensurface shape variables. Based on this result 97.9% of the training set species were assigned to their correct flight-speed groups on the basis of proximity of their projected positions to the group means. Shape models below the ordination plot represent along-axis coordinate locations through the canonical variates space for CV-1 calculated using the method of MacLeod (2007). Major differences can be seen in the size of the deltoid crest (DC) and the bicipital crest (BC), and in species with lower scores the bicipital surface (BS) is larger and more rounded, forming a dome. Note the CV-2 axis contains no information with regard to group discrimination and should not be interpreted. Species abbreviations are listed in Appendix 1.
Figure 6 in Eigensurface analysis, ecology, and modelling of morphological adaptation in the falconiform humerus (Falconiformes: Aves)
Figure 6. Models of the first three eigensurface (E-Surf) axes that describe the distribution of morphology among the 50 humerus specimens. Eigensurface axis 1 describes 41.8% of observed shape variation and shows clear differences in the shapes of the deltoid and bicipital crests between high and low scoring specimens. Eigensurface axis 2 accounts for 12.8% of morphological variation and describes more subtle variation in the shape of the deltoid crest. Eigensurface axis 3 includes 7.78% of surface shape variation and exhibits differences in the shape and position of the deltoid and bicipital crests between specimens. See text for further discussion of the shape changes and interpretation of the morphological variation described by these model axes.
Figure 9 in Eigensurface analysis, ecology, and modelling of morphological adaptation in the falconiform humerus (Falconiformes: Aves)
Figure 9. Ordination of the falconiform species for which foraging flight-style information was available (42 species) within the space of the four canonical variates axes established in a CVA using 13 eigensurface shape variables. The distribution of humerus shapes on the first two CV axes (above) together accounted for 73.7% of between-groups humeral shape variation, while CV-3 and CV-4 (below) together represent the remaining 26.3% of the variation used to distinguish between the five flight-style groups: perch-hunting, chasing, hovering, soaring, and low-flight. Based on this result 88.1% of training set species were assigned to their correct flight-style groups on the basis of proximity to the group means. Shape models representing along-axis coordinate positions through the canonical variates space are shown in Figure 10, highlighting morphological features that were particularly important in distinguishing between high- and low-scoring species on each CV axis. Species abbreviations are listed in Appendix 1.
Figure 4 in Eigensurface analysis, ecology, and modelling of morphological adaptation in the falconiform humerus (Falconiformes: Aves)
Figure 4. Steps in the definition of eigensurface sampling grids as exemplified by the three scans of the proximal–dorsal surfaces of the humeri illustrated in Figure 3. The upper row shows the region selected for analysis. Point clouds of approximately 2000–3000 points representing this region were saved as ASCII text files along with separate files recording the boundary outline coordinates, points along a midline, and the coordinate positions of the two landmarks selected to orient the grid. Lower row: eigensurface form sampling grids. Each eigensurface grid is calculated by selecting a grid resolution (e.g. 10, 15, 20) and then interpolating that number of equally spaced semilandmark points along each half-outline (black) and along the surface trace of the chord joining the orientation landmarks (white). In this analysis a grid resolution of 10 was selected and the landmark chord oriented so that it traced the approximate position of the mid-line running from the humerus head down the centre of the shaft. Lateral or 'rib' chords are then drawn along the surface of the form such that each mid-line node is joined to a boundary outline node on either side. Equally spaced rib semilandmarks (grey) were then located along each of these rib chords with the number of semilandmarks used to quantify the shape of the chord being set iteratively as the number required to represent 95% of the length of the most contorted corresponding chord across the entire sample. This iterative procedure is identical to that used by MacLeod (1999) to sample boundary outline form in extended eigenshape analysis. The resulting grids quantify the geometric form of the surface of the humerus using an equal number of semilandmark points for each specimen in the sample and with each point being located in a position that corresponds topologically (relative to the grid point set as a whole) to all other points across the sample.
Figure 2 in Eigensurface analysis, ecology, and modelling of morphological adaptation in the falconiform humerus (Falconiformes: Aves)
Figure 2. Phylogeny of Falconiformes based on Griffiths et al. (2004), Lerner & Mindell (2005), Lerner et al. (2008) and Griffiths et al. (2007). Species are grouped by their ecological or vernacular names. Size of the wedges indicates species richness. Genus or species names of taxa, along with the number of species from each genus included in the study dataset, are indicated after each clade name. Specimens were selected to be representative of overall morphological, ecological, and behavioural diversity within their group. Lineages shown in grey were not included in this investigation.
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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
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