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42 results for “Small-Bodies”
Figure 9 in Osteology and phylogeny of small-bodied hadrosauromorphs from an end-Cretaceous marine assemblage
Figure 9. Additional hadrosaurid material from the West Jersey Marl Pit Co. site and Gloucester County. YPM 1600, the holotype of 'Hadrosaurus minor' in (A) lateral and (B) posterior views. YPM 1593, caudal centrum, in (C) lateral and (D) posterior views. Juvenile hadrosauromorph coracoid YPM 7898 in (E) medial and (F) lateral views.
Figure 1 in Osteology and phylogeny of small-bodied hadrosauromorphs from an end-Cretaceous marine assemblage
Figure 1. Locality information and skeletal diagrams. Location of the West Jersey Marl Co. Pit site in Gloucester County, New Jersey (A). Skeletal diagrams showing preserved elements in (B) YPM 745, (C) a composite of additional small hadrosauromorph materials from the West Jersey Marl Co. Pit site, and (D) YPM 7896 in Gloucester County, New Jersey.
Figure 5 in Osteology and phylogeny of small-bodied hadrosauromorphs from an end-Cretaceous marine assemblage
Figure 5. Plot of length (horizontal axis) against width (vertical axis) for a variety of hadrosaurids and hadrosauromorphs. Arrow and silhouette indicate the point corresponding to YPM 745.
Figure 8 in Osteology and phylogeny of small-bodied hadrosauromorphs from an end-Cretaceous marine assemblage
Figure 8. Fibulae and astragalus of YPM 7896. Fibula in (A) lateral, (B) medial, (C) anterior and (D) proximal views. Astragalus in (F) posterior, (G) anterior, (H) dorsal and (I) ventral views, with a photograph (E) of the medial surface showing region with distinct, pitted bone texture and colour.
Figure 3 in Osteology and phylogeny of small-bodied hadrosauromorphs from an end-Cretaceous marine assemblage
Figure 3. Femur of YPM 745. Femur in YPM 745 in (A) posterior, (B) medial, (C) lateral and (D) proximal views.
Figure 2 in Osteology and phylogeny of small-bodied hadrosauromorphs from an end-Cretaceous marine assemblage
Figure 2. Vertebrae and ribs of YPM 745. Complete rib in (A) anterior, (B) posterior and (C) lateral views. Partial rib in (D) anterior and (E) posterior views. Vertebral centra fragments in (F, H, J) dorsal?, (G, K, I) ventral? and (L) anterior? views.
Figure 7 in Osteology and phylogeny of small-bodied hadrosauromorphs from an end-Cretaceous marine assemblage
Figure 7. Tibia of YPM 7896 Right tibia in YPM 7896 in (A) lateral, (B) posterior, (C) medial, (D) anterior and (E) proximal views.
Figure 6 in Osteology and phylogeny of small-bodied hadrosauromorphs from an end-Cretaceous marine assemblage
Figure 6. Tibia of YPM 745. Right tibia in YPM 745 in (A) medial, (B) anterior, (C) posterior, and (D) lateral views.
Figure 10 in Osteology and phylogeny of small-bodied hadrosauromorphs from an end-Cretaceous marine assemblage
Figure 10. Phylogeography of Hadrosauroidea, including YPM 745. (A) map showing a biogeographic hypothesis for latest Cretaceous hadrosauromorphs in North America. (B) time-calibrated strict consensus tree of Hadrosauromorpha found in the analysis including YPM 745.
Data from: Cryptic genetic diversity is paramount in small-bodied amphibians of the genus Euparkerella (Anura: Craugastoridae) endemic to the Brazilian Atlantic Forest
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Skin swabbing protocol to collect DNA samples from small-bodied fish species
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Histological and life history data for small-bodied mammals from: Multituberculate mammals show evidence of a life history strategy similar to that of placentals, not marsupials
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Data from: New small-bodied ornithopods (Dinosauria, Neornithischia) from the Early Cretaceous Wonthaggi Formation (Strzelecki Group) of the Australian-Antarctic rift system, with revision of Qantassaurus intrepidus Rich and Vickers-Rich, 1999
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Data from: Senescence or selective disappearance? Age trajectories of body mass in wild and captive populations of a small-bodied primate
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Data from: Methodological considerations for detection of terrestrial small-body salamander eDNA and implications for biodiversity conservation
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(Ceríaco et al. 2016a:27); "Espinheira" [-16.78886, 12.35761] (Ceríaco et al. 2016a:28). Taxonomic and distributional notes: Rhoptropus biporosus is closely allied to R. barnardi and one or more undescribed species of small-bodied congeners that occupy similar habitats in arid to semi-arid rocky areas bordering the Namib (Kuhn 2016). MAP 150. Distribution of Rhoptropus biporosus in Angola. in Diversity and Distribution of the Amphibians and Terrestrial Reptiles of Angola Atlas of Historical and Bibliographic Records (1840-2017)
(Ceríaco et al. 2016a:27); "Espinheira" [-16.78886, 12.35761] (Ceríaco et al. 2016a:28). Taxonomic and distributional notes: Rhoptropus biporosus is closely allied to R. barnardi and one or more undescribed species of small-bodied congeners that occupy similar habitats in arid to semi-arid rocky areas bordering the Namib (Kuhn 2016). MAP 150. Distribution of Rhoptropus biporosus in Angola.
Data from: Livestock grazing reinforces the competitive exclusion of small-bodied birds by large aggressive birds
1.Grazing by domestic livestock is sometimes promoted as a management tool to benefit biodiversity. In many situations, however, it can produce negative outcomes. 2.Here we examine the impacts of recent and historic livestock grazing on bird communities in the semi-arid woodlands in eastern Australia, testing the notion that grazing removes the suppressive effect of structurally complex vegetation on miners, thereby reducing the richness and abundance of small birds. 3.We used time- and area-limited searches of 108 sites varying in livestock grazing history and intensity, to explore the direct and indirect effects of grazing, habitat complexity and the abundance of aggressive, large-bodied birds on smaller-bodied birds using two-way analysis of variance and structural equation modelling. 4.Small birds were less abundant and had lower richness in the presence of miners. Our structural equation models indicated that recent grazing had direct suppressive effects on the abundance of miners, and both richness and abundance of all but the largest-bodied bird groups. However, higher levels of historic livestock grazing reinforced the competitive exclusion of the six small-bodied bird groups (insectivores, nectarivores, declining woodland birds, small ground foraging birds, all small birds, all non-miners) by aggressive miners via reductions in habitat complexity. Moreover, the strength of any suppressive effects on small birds or positive effects on large birds by miners increased with increasing miner abundance. 5.Synthesis and applications. Our results highlight the importance of vegetation structural complexity, not only for providing habitat for woodland birds, but as barriers to the invasion and competitive dominance of miners. Our findings suggest that management actions aimed at reducing tree and shrub density to promote open woodlands are likely to have significant negative consequences for the conservation of small woodland birds.
Data from: Livestock grazing reinforces the competitive exclusion of small-bodied birds by large aggressive birds
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Data from: A small-bodied species of Brontotheriidae from the middle Eocene Nut Beds of the Clarno Formation, John Day Basin, Oregon
We diagnose a new species of Brontotheriidae from a middle Eocene locality, the Clarno Nut Beds, from the Clarno Formation, John Day Basin, Central Oregon. Though renowned for its richness in fossil flora, fossil vertebrates are rare in the Clarno Nut Beds and this new species is the most abundantly represented mammal. Radiometric dating constrains the age of the Nut Beds fauna to about 43.76 Ma within the Uintan North American Land Mammal Age. This new taxon, represented by numerous cranial, mandibular, and dental specimens, is comparatively small for a brontothere and notable for its cranio-caudally shorted nasal incision, a trait shared with three larger-bodied middle Eocene species, Metatelmatherium ultimum, Wickia brevirhinus, and Sthenodectes incisivum. Phylogenetic analysis suggests the sister taxon of the Nut Beds brontothere could be one of two species—Wickia brevirhinus from the Sand Wash Basin of Colorado and Washakie Formation of Wyoming, or Metatelmatherium ultimum, a pan-Beringian species known from the Uintan Formation of Utah (and other Uintan age deposits) and the "Irdin Manha" Formation of Inner Mongolia, China. Phylogenetic results also indicate that the Nut Beds brontothere is a dwarf taxon. Though brontotheres are renowned for having evolved very large body sizes, this new brontothere is one of several discovered in recent decades that suggest evolutionary reductions in body size may have been relatively common in Brontotheriidae.
Data from: Minimally invasive collection of adipose tissue facilitates the study of eco-physiology in small-bodied mammals
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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.