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325 results for “Distribution limits”
Data from: Loss of fungal symbionts at the arid limit of the distribution range in a native Patagonian grass – resource ecophysiological relations
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Data from: Ecophysiological limits to aerobic metabolism in hypoxia determine epibenthic distributions and energy sequestration in the northeast Pacific ocean
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Data from: From the individual to the landscape and back: Time-varying effects of climate and herbivory on tree sapling growth at distribution limits
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The role of dispersal limitation and reforestation in shaping the distributional shift of a forest herb under climate change
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Data from: Numbers and distribution of the Great Cormorant in Iceland: limitation at the regional and metapopulation level
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Data from: Ecological correlates of the distribution limits of two poeciliid species across a salinity gradient
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Data from: Phenotype-limited distributions: short-billed birds move away during times that prey bury deeply
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Distribution. Lowlands of Malay Peninsula; exact distributional limits are not well established. in Rhinolophidae
Distribution. Lowlands of Malay Peninsula; exact distributional limits are not well established.
Figure 5 in Demographic characteristics, seasonal range and habitat topography of Balkan chamois population in its southernmost limit of its distribution (Giona mountain, Greece)
Figure 5. Used elevation, inclination (violin plots) and aspect (histogram) of the Balkan chamois in Giona Mt. Black lines in the violin plots indicate 95% probability of occurrence in terms of Fixed Kernel Density Estimator and white dots indicate median values.
Figure 4. Seasonal range generated from a in Demographic characteristics, seasonal range and habitat topography of Balkan chamois population in its southernmost limit of its distribution (Giona mountain, Greece)
Figure 4. Seasonal range generated from a Fixed Kernel Density Estimator (FKDE) (95% probability) and respective core areas of Balkan chamois in Giona Mt for (A) winter, (B) spring, (C) summer and (D) autumn. In the upper right corner the diagram presents the delineation of the probability of species occurrence within the core area.
Figure 3 in Demographic characteristics, seasonal range and habitat topography of Balkan chamois population in its southernmost limit of its distribution (Giona mountain, Greece)
Figure 3. Annual range and core area of Balkan chamois in the study area, and overlap with the Natura 2000 site in Giona Mt.
Figure 1 in Demographic characteristics, seasonal range and habitat topography of Balkan chamois population in its southernmost limit of its distribution (Giona mountain, Greece)
Figure 1. Balkan chamois distribution in Greece, modified from Papaioannou and Kati 2007 (see Appendix 1).
The environmental factors limiting the distribution of shallow-water terebratulid brachiopods
<p class="western"><span><span>The Cenozoic genus <i>Terebratula</i> seems to be an exception to the Post-Permian trend in brachiopod retreat to offshore habitats because it was species-rich and numerically abundant in warm-temperate shallow-water environments in the Mediterranean and the Paratethys realms. This was so despite the general dominance of bivalves and the pervasive bioturbation and predation pressure during the Neogene. <i>Terebratula</i>, however, went extinct in the Calabrian (Pleistocene). The optimal environmental conditions for <i>Terebratula </i>during its prime are poorly known. The Águilas Basin (SE Spain) is an ideal study area to investigate the habitat of <i>Terebratula</i> because shell beds of this brachiopod occur there cyclically in early Pliocene deposits. We evaluate the paleoecological boundary conditions controlling the distribution of <i>Terebratula </i>by estimating its environmental tolerances using benthic and planktic foraminiferal and nannoplankton assemblages and oxygen isotopes of the secondary layer brachiopod calcite. Our results suggest that <i>Terebratula </i>in the Águilas Basin favored oligotrophic to mesotrophic, well-oxygenated environments at water depths of 60-90 m. Planktic foraminiferal assemblages and oxygen isotopes point to sea-surface temperatures between ~16 and 22ºC, and bottom-water temperatures between 17 and 24ºC. The analyzed proxies indicate that <i>Terebratula </i>tolerated local variations in water depth, bottom temperature, oxygenation, productivity and organic enrichment. <i>Terebratula</i> was probably excluded by grazing pressure from well-lit environments and preferentially occupied sediment-starved, current-swept upper offshore habitats where coralline red algae were absent. Narrow temperature ranges of <i>Terebratula</i> species might have been a disadvantage during the high-amplitude seawater temperature fluctuations that started about 1 Myr ago, when the genus went extinct.</span></span></p>
FIGURE 13 in The Akodon boliviensis species group (Rodentia: Cricetidae: Sigmodontinae) in Argentina: species limits and distribution, with the description of a new entity
FIGURE 13. Akodon polopi, new species (holotype MACN 23486): live trapped specimen.
Distribution. NE & EC Madagascar, but precise limits unknown. in Cheirogaleidae
Distribution. NE & EC Madagascar, but precise limits unknown.
Distribution. NW & CW Argentina; limits unresolved. in Cricetidae
Distribution. NW & CW Argentina; limits unresolved.
Distribution. EC Panama; limits unresolved. in Cricetidae
Distribution. EC Panama; limits unresolved.
Distribution. Limited to Pacific slope of Sierra de Miahuatlan, S Oaxaca, Mexico. in Cricetidae
Distribution. Limited to Pacific slope of Sierra de Miahuatlan, S Oaxaca, Mexico.
Distribution. SW China (W Sichuan and Yunnan); distributional limits are unclear. in Soricidae
Distribution. SW China (W Sichuan and Yunnan); distributional limits are unclear.
Distribution. Kenya and Tanzania; N limits not known. in Muridae
Distribution. Kenya and Tanzania; N limits not known.
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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.