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172 results for “ranging patterns”
SGS-LTER Standard Production Data: 1983-2008 Annual Aboveground Net Primary Production on the Central Plains Experimental Range, Nunn, Colorado, USA 1983-2008, ARS Study Number 6 (Reformatted to the ecocomDP Design Pattern)
This data package is formatted as an ecocomDP (Ecological Community Data Pattern). For more information on ecocomDP see https://github.com/EDIorg/ecocomDP. This Level 1 data package was derived from the Level 0 data package found here: https://pasta.lternet.edu/package/metadata/eml/knb-lter-sgs/700/1. The abstract below was extracted from the Level 0 data package and is included for context: This data package was produced by researchers working on the Shortgrass Steppe Long Term Ecological Research (SGS-LTER) Project, administered at Colorado State University. Long-term datasets and background information (proposals, reports, photographs, etc.) on the SGS-LTER project are contained in a comprehensive project collection within the Digital Collections of Colorado (http://digitool.library.colostate.edu/R/?func=collections&collection_id=3429). The data table and associated metadata document, which is generated in Ecological Metadata Language, may be available through other repositories serving the ecological research community and represent components of the larger SGS-LTER project collection. The objective of the long-term ANPP study is to monitor long-term net above ground primary production of the shortgrass steppe community by species. There are 6 sites: ridgetop (ridge), midslope (mid), swale, ESA (replicate 1 not 2), Section 25 (SEC 25), and owl-creek (OC). Each site is located in a different landscape position or soil type on the shortgrass steppe and may be grazed or not. Ridgetop, midslope and swale are grazed and are sampled along a catena. Section 25 is grazed and is located in an upload grassland. ESA is an ungrazed upland grassland an is the control from the Ecosystem Stress Area experiment. Owl Creek is ungrazed and is located in the lowland along the owl creek drainage. There are 3 transects with 5 plots in each transect. Plots in the grazed locations are protected by cages. Because this is a monitoring effort, true replicates across the landscape are not
SGS-LTER Long-Term Monitoring Project: Vegetation Cover on Small Mammal Trapping Webs on the Central Plains Experimental Range, Nunn, Colorado, USA 1999 -2006, ARS Study Number 118 (Reformatted to the ecocomDP Design Pattern)
This data package is formatted as an ecocomDP (Ecological Community Data Pattern). For more information on ecocomDP see https://github.com/EDIorg/ecocomDP. This Level 1 data package was derived from the Level 0 data package found here: https://pasta.lternet.edu/package/metadata/eml/knb-lter-sgs/140/17. The abstract below was extracted from the Level 0 data package and is included for context: This data package was produced by researchers working on the Shortgrass Steppe Long Term Ecological Research (SGS-LTER) Project, administered at Colorado State University. Long-term datasets and background information (proposals, reports, photographs, etc.) on the SGS-LTER project are contained in a comprehensive project collection within the Digital Collections of Colorado (http://digitool.library.colostate.edu/R/?func=collections&collection_id=3429). The data table and associated metadata document, which is generated in Ecological Metadata Language, may be available through other repositories serving the ecological research community and represent components of the larger SGS-LTER project collection. Additional information and referenced materials can be found: http://hdl.handle.net/10217/83458. The abundance and diversity of small mammals in shortgrass steppe is strongly influenced by the structure and composition of vegetation. Vegetation structure provides cover from predators and harsh abiotic conditions. Plant species composition affects the types of seeds and herbaceous material available to granivores and herbivores, and influences arthropod populations, which are important prey for the omnivorous species that dominate in shortgrass steppe. Both vegetation structure and plant community composition are sensitive to the availability of precipitation as well as the activity of large mammalian herbivores. In 1999, we began measuring vegetation structure and plant community composition on the three grassland and three shrubland trapping webs where we live-trap small mammals
SGS-LTER Long-term Monitoring Project: Spotlight Rabbit Count on the Central Plains Experimental Range, Nunn, Colorado, USA 1994-2006, ARS Study Number 98 (Reformatted to the ecocomDP Design Pattern)
This data package is formatted as an ecocomDP (Ecological Community Data Pattern). For more information on ecocomDP see https://github.com/EDIorg/ecocomDP. This Level 1 data package was derived from the Level 0 data package found here: https://pasta.lternet.edu/package/metadata/eml/knb-lter-sgs/136/17. The abstract below was extracted from the Level 0 data package and is included for context: This data package was produced by researchers working on the Shortgrass Steppe Long Term Ecological Research (SGS-LTER) Project, administered at Colorado State University. Long-term datasets and background information (proposals, reports, photographs, etc.) on the SGS-LTER project are contained in a comprehensive project collection within the Digital Collections of Colorado (http://digitool.library.colostate.edu/R/?func=collections&collection_id=3429). The data table and associated metadata document, which is generated in Ecological Metadata Language, may be available through other repositories serving the ecological research community and represent components of the larger SGS-LTER project collection. Additional information and referenced materials can be found: http://hdl.handle.net/10217/83448. Rabbits are the most important small-mammal herbivores in shortgrass steppe, and may significant influence the physiognomy and population dynamics of herbaceous plants and woody shrubs. Rabbits also are the most important prey of mammalian carnivores such as coyotes and large raptors such as golden eagles and great horned owls. Two hares (Lepus californicus, L. townsendii) and one cottontail rabbit (Sylvilagus audubonii) occur in shortgrass steppe. In 1994, we initiated long-term studies to track changes in relative abundance of rabbits on the Central Plains Experimental Range (CPER). On four nights each year (one night each season, usually on new moon nights in January, April, July, October), we drove a 32-km route consisting of pasture two-track and gravel roads on the CPER. This wa
SGS-LTER Long-Term Montioring Project: Arthropod Pitfall Trapping on Small Mammal Trapping Webs on the Central Plains Experimental Range, Nunn, Colorado, USA 1998-2006, ARS Study Number 118 (Reformatted to the ecocomDP Design Pattern)
This data package is formatted as an ecocomDP (Ecological Community Data Pattern). For more information on ecocomDP see https://github.com/EDIorg/ecocomDP. This Level 1 data package was derived from the Level 0 data package found here: https://pasta.lternet.edu/package/metadata/eml/knb-lter-sgs/134/17. The abstract below was extracted from the Level 0 data package and is included for context: This data package was produced by researchers working on the Shortgrass Steppe Long Term Ecological Research (SGS-LTER) Project, administered at Colorado State University. Long-term datasets and background information (proposals, reports, photographs, etc.) on the SGS-LTER project are contained in a comprehensive project collection within the Digital Collections of Colorado (http://digitool.library.colostate.edu/R/?func=collections&collection_id=3429). The data table and associated metadata document, which is generated in Ecological Metadata Language, may be available through other repositories serving the ecological research community and represent components of the larger SGS-LTER project collection. Additional information and referenced materials can be found: http://hdl.handle.net/10217/83450. With the exception of heteromyids, eg kangaroo rats and pocket mice, most small rodents in shortgrass steppe are omnivorous. Depending on season, arthropods (insects and arachnids) make up 40-85% of the diet of grasshopper mice and thirteen-lined ground squirrels, the most widespread rodents in northern shortgrass steppe. Small mammals are among the most important predators of ground-dwelling macroarthropods and herbivorous insects provide a direct resource link between weather and plant production. Understanding temporal variability in the abundance of arthropods is central to determining the mechanisms that drive small rodent populations. At present, there are no long-term studies of arthropods in shortgrass steppe, despite the important role that these taxa play in grassland food w
SGS-LTER Long-Term Monitoring Project: Small Mammals on Trapping Webs on the Central Plains Experimental Range, Nunn, Colorado, USA 1994 -2006, ARS Study Number 118 (Reformatted to the ecocomDP Design Pattern)
This data package is formatted as an ecocomDP (Ecological Community Data Pattern). For more information on ecocomDP see https://github.com/EDIorg/ecocomDP. This Level 1 data package was derived from the Level 0 data package found here: https://pasta.lternet.edu/package/metadata/eml/knb-lter-sgs/137/17. The abstract below was extracted from the Level 0 data package and is included for context: This data package was produced by researchers working on the Shortgrass Steppe Long Term Ecological Research (SGS-LTER) Project, administered at Colorado State University. Long-term datasets and background information (proposals, reports, photographs, etc.) on the SGS-LTER project are contained in a comprehensive project collection within the Digital Collections of Colorado (http://digitool.library.colostate.edu/R/?func=collections&collection_id=3429). The data table and associated metadata document, which is generated in Ecological Metadata Language, may be available through other repositories serving the ecological research community and represent components of the larger SGS-LTER project collection. Additional information and referenced materials can be found: http://hdl.handle.net/10217/83452. Small mammals (rabbits, rodents) are integral components of semiarid ecosystems because of their roles as consumers of plants, seeds and arthropods, as soil disturbance agents, and as food for raptors, snakes and mammalian carnivores. Because of their vagility and intermediate trophic position, populations of small mammals may track changes in vegetation and the abiotic environment that may result from shifts in land-use and other anthropogenic disturbances. However, these populations are variable over space and time, and their response to environmental changes may not be immediately apparent given their behavioral flexibility and relatively long life-spans and generation times. Patterns in the distribution and abundance of small mammals thus may simultaneously reflect and affect the
SGS-LTER Ecosystem Stress Area - long-term density dataset following nutrient enrichment stress on the Central Plains Experimental Range in Nunn, Colorado, USA 1975-2011, ARS Study Number 3 (Reformatted to the ecocomDP Design Pattern)
This data package is formatted as an ecocomDP (Ecological Community Data Pattern). For more information on ecocomDP see https://github.com/EDIorg/ecocomDP. This Level 1 data package was derived from the Level 0 data package found here: https://pasta.lternet.edu/package/metadata/eml/knb-lter-sgs/520/8. The abstract below was extracted from the Level 0 data package and is included for context: This data package was produced by researchers working on the Shortgrass Steppe Long Term Ecological Research (SGS-LTER) Project, administered at Colorado State University. Long-term datasets and background information (proposals, reports, photographs, etc.) on the SGS-LTER project are contained in a comprehensive project collection within the Digital Collections of Colorado (http://digitool.library.colostate.edu/R/?func=collections&collection_id=3429). The data table and associated metadata document, which is generated in Ecological Metadata Language, may be available through other repositories serving the ecological research community and represent components of the larger SGS-LTER project collection. Water, nitrogen, and water-plus-nitrogen at levels beyond the range normally experience by shortgrass steppe communities were applied from 1971 through 1975, plant densities were sampled through 1977, and then sampling resumed in 1982, with sampling frequencies changing from annually to every other year. The initial sampling from 1970 to 1974 showed that the water and water plus nitrogen treatments had the strongest effect on plant community structure, both treatments increased biomass, and exotic weed species were noted on the water plus nitrogen treatment. Later sampling from 1982 to 1991 showed a ten-fold increase in exotic weed species on the water plus nitrogen plots as compared to the controls (Milchunas and Lauenroth 1995), a community change that has persisted on this site due to a chronic elevation of soil nitrogen caused by a plant tissue/soil organic matter feedback mec
SGS-LTER Ecosystem Stress Area - long-term point-frame (percent basal cover) dataset following nutrient enrichment stress on the Central Plains Experimental Range in Nunn, Colorado, USA 1982-2011, ARS Study Number 3 (Reformatted to the ecocomDP Design Pattern)
This data package is formatted as an ecocomDP (Ecological Community Data Pattern). For more information on ecocomDP see https://github.com/EDIorg/ecocomDP. This Level 1 data package was derived from the Level 0 data package found here: https://pasta.lternet.edu/package/metadata/eml/knb-lter-sgs/521/7. The abstract below was extracted from the Level 0 data package and is included for context: This data package was produced by researchers working on the Shortgrass Steppe Long Term Ecological Research (SGS-LTER) Project, administered at Colorado State University. Long-term datasets and background information (proposals, reports, photographs, etc.) on the SGS-LTER project are contained in a comprehensive project collection within the Digital Collections of Colorado (http://digitool.library.colostate.edu/R/?func=collections&collection_id=3429). The data table and associated metadata document, which is generated in Ecological Metadata Language, may be available through other repositories serving the ecological research community and represent components of the larger SGS-LTER project collection. Water, nitrogen, and water-plus-nitrogen at levels beyond the range normally experience by shortgrass steppe communities were applied from 1971 through 1975, plant densities were sampled through 1977, and then sampling resumed in 1982, with sampling frequencies changing from annually to every other year. The initial sampling from 1970 to 1974 showed that the water and water plus nitrogen treatments had the strongest effect on plant community structure, both treatments increased biomass, and exotic weed species were noted on the water plus nitrogen treatment. Later sampling from 1982 to 1991 showed a ten-fold increase in exotic weed species on the water plus nitrogen plots as compared to the controls (Milchunas and Lauenroth 1995), a community change that has persisted on this site due to a chronic elevation of soil nitrogen caused by a plant tissue/soil organic matter feedback mec
Data from: Occupancy patterns and upper range limits of lowland Bornean birds along an elevational gradient
<p>Aim: The traditional view of species' distributions is that they are less abundant near the edges of their ranges and more abundant toward the center. Testing this pattern is difficult because of the complexity of distributions across wide geographical areas. An alternative strategy, however, is to measure species' distributional patterns along elevational gradients. We applied this strategy to examine whether lowland forest birds are indeed less common near their upper range limits on a Bornean mountain, and tested co-occurrence patterns among species for potential causes of attenuation, including signatures of habitat selection and competition at the periphery of their ranges.</p> <p>Location: Mt. Mulu, Borneo</p> <p>Taxon: Rain forest birds Methods: We surveyed lowland forest birds on Mt. Mulu (2,376 m), classified their elevation-occupancy distributions using Huisman – Olff – Fresco (HOF) models, and examined co-occurrence patterns of species pairs for signatures of shared habitat patches and interspecific competition.</p> <p>Results: For 39 of 50 common species, occupancy was highest at sea level then gradually declined near their upper range edges, in keeping with a 'rare periphery' hypothesis. With respect to habitat selection, lowland species do not appear to cluster together at sites of patchy similar habitat near their upper range limits; neither are most lowland species segregated from potential montane competitors where ranges overlap.</p> <p>Main conclusions: High relative abundance at sea level implies that species inhabit 'truncated niches' and are not currently near the limits of their fundamental niche, unless unknown critical response thresholds exist. However, indirect effects of increasing temperature predicted under climate change scenarios could still influence lower range limits of lowland species indirectly by altering habitat, precipitation regimes, and competitive interactions. The lack of non-random co-occurrence patterns implies that patchy habitat and simple pairwise species interactions are unlikely to be responsible for upper range limits in most species; diffuse competition across diverse rain forest bird communities could still play a role.</p>
Fig.1 in Home range, movements and activity patterns of an exceptionally large male Brown Bear (Ursus arctos L.) in the area of the Bulgarian-Greek border (Western Rhodope Mts.)
Fig.1. Dominant male (supposed age of at least 15 years old) with scars of battles with rivals. Hunting Forestry Adjilarska (photo from a kamera-trap, D. Bukovsky, 17.03.2014 at a game-feeding station).
Fig 2. A in Home range, movements and activity patterns of an exceptionally large male Brown Bear (Ursus arctos L.) in the area of the Bulgarian-Greek border (Western Rhodope Mts.)
Fig 2. A century-old bear marking tree just on the Bulgarian/Greek border. The tree is marked also with white paint as a border pillar (photo N. Spassov).
Figure3. APCs A1-A4 connected within range of cohesion-factor-threshold form members of one ARB-AIDEN: A Density Conscious Artificial Immune System for Automatic Discovery of Arbitrary Shape Clusters in Spatial Patterns
<p>Figure3 depicts this process. The<br> model with the above specification then effectively detects self or non-self pathogens. In terms of<br> its application to the task of clustering, this interpretation means making the affinities high within<br> clusters and low across clusters. A pathogen corresponding to an outlier would not stimulate a TCR<br> sufficiently and may not form part of any ARB.</p>
Fig. 1 in The Study Of Age-Related Variability Of Pigmentation Patterns Of The Shells Of Dreissena Polymorpha (Bivalvia, Dreissenidae) From Different Parts Of It'S Range
Fig. 1. Change of pattern types on zebra mussel shell. The present shell has four age zones (0+, 1+, 2+, 3+). The pattern sequence is С–АС–А–А.
Figure. General head scalation pattern for Elaphe sauromates (cs – anterior chin shields; cs' – posterior chin shields; f – frontal; g – gulars; in – internasal; l – loreal; la – upper labials; la' – lower labials; m – mental; p – parietals; pf – prefrontal; prn – prenasal; ptn – postnasal; pto – postocular; pro – preocular; r – rostral; so – supraocular; sbo – subocular; t – temporals; v – ventral shields). in Morphological characteristics of the elusive blotched snake (Elaphe sauromates) at its northwestern range limit (Romania)
Figure. General head scalation pattern for Elaphe sauromates (cs – anterior chin shields; cs' – posterior chin shields; f – frontal; g – gulars; in – internasal; l – loreal; la – upper labials; la' – lower labials; m – mental; p – parietals; pf – prefrontal; prn – prenasal; ptn – postnasal; pto – postocular; pro – preocular; r – rostral; so – supraocular; sbo – subocular; t – temporals; v – ventral shields).
Elevational range size patterns of vascular plants in Himalaya contradict Rapoport's rule
<p>1. Elevational range size patterns reflect ecological and evolutionary processes, but they are also affected by geometric constraints. The confounding effect of these constraints led to an ongoing controversy about the elevational Rapoport's rule, which postulates a positive association between the range size and elevation, and about the plausibility of the climate variability hypotheses as its causal explanation.</p> <p>2. Here we used an advanced null modelling approach to disentangle the interacting effects of geometric constraints and species richness gradients on the elevational range size of vascular plants. We collected extensive field data on elevational distribution for 728 vascular plant species occurring in the Ladakh region, Western Himalaya. We supplied these regional data with sub-continental elevational ranges extracted from the literature. Moreover, we used in-situ measured temperatures to quantify temperature variability along an elevational gradient to test the climate variability hypothesis.</p> <p>3. Observed range size patterns were sensitive to methods used to quantify the average range size. Range truncation disproportionately affected regional ranges of low-elevation species and resulted in spurious support of elevational Rapoport's rule. However, when the confounding effects of domain boundaries and richness gradient were controlled, our null models revealed only slight deviations from the random expectations of elevational range size patterns, contrasting with the prediction of the Rapoport's rule. In line with these findings, seasonal and diurnal temperature variability did not change with elevation.</p> <p>4. Synthesis: Geometric constraints combined with underlying species richness gradient create range size patterns seemingly supporting Rapoport´s elevational rule. However, null models accounting for these effects indicate that the range-size of vascular plants in the Himalayas does not increase with elevation. Given the universality of the geometric constraints and species richness gradient, our results suggest that these confounding factors must be controlled when testing Rapoport's rule. The null model approach described here provides an efficient tool to do that.</p>
Fig. 2 in Home range and activity patterns of Sunda scops owl in Peninsular Malaysia
Fig. 2. Home range pattern generated by each of the six radiotracked owls, based on 95% MCP (shaded area) and HM (nonshaded area) methods.
Data from: Non-breeding sites, loop migration and activity patterns over the annual cycle in the Lesser Grey Shrike Lanius minor from a western edge of its range
<p>Raw data from three tracked individuals. Two were tracked with light geolocators (22UL and an incomplete track of 22UH) and one (16KN) with GDL3-PAM multi-sensor logger. All produced by Swisss Ornithological Insitute.</p>
Associated Dataset for Genome-wide DNA methylation patterns in bumble bee (Bombus vosnesenskii) populations from spatial-environmental range extremes
<p>The dataset contains the final methylation call set (n=14,627,533), variant calling file for population genomics analyses, analysis codes/scripts, and other associated files related to the research (Constitutive and variable patterns of genome-wide DNA methylation in populations from spatial-environmental range extremes of the bumble bee <em>Bombus vosnesenskii)</em>. Raw WGBS reads generated in this study have been deposited and are currently available at the National Center for Biotechnology Information (NCBI) Sequence Read Archive (SRA) under NCBI BioProject PRJNA956115.</p>
Data from: Occupancy patterns and upper range limits of lowland Bornean birds along an elevational gradient
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Elevational range size patterns of vascular plants in Himalaya contradict Rapoport’s rule
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Drivers and mechanisms that contribute to microbial β-diversity patterns and range sizes in mountains across a climatic variability gradient
<p>Microbial communities are highly diverse, yet the mechanisms underlying microbial community assembly are not well understood. Janzen's mountain passes hypothesis proposed that climatic barriers and dispersal limitation shape communities to a greater extent in mountains with lower climatic variability and overlap, permitting higher levels of species coexistence. Here, we investigate changes in microbial community dissimilarities, distributional range sizes and ecological processes along elevational gradients in three montane ecosystems representing a climatic variability gradient. We found that climate, climatic variability and spatial distance play dominating roles in affecting microbial β-diversity patterns and range sizes along elevational gradients. Janzen's mountain passes hypothesis can be applied for microbial community assembly: mountains with lower climatic variability and higher climatic difference between elevations exhibited higher β-diversity, higher endemism, lower range sizes, and steeper distance-decay trends. However, microbial communities experience clear climate-driven limited range sizes and dispersal processes and show typical endemic patterns in all mountain ecosystems. Our results emphasize the importance of dispersal and climatic niche processes in shaping montane biodiversity. As a result, changes in climate may significantly impact soil biodiversity in montane ecosystems by altering the effects of dispersal limitation and climatic variability on bacterial and fungal community composition along elevational gradients.</p>
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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.