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411 results for “spatial variation”
Data from: Spatial and host-related variation in prevalence and population density of wheat curl mite (Aceria tosichella) cryptic genotypes in agricultural landscapes
<p><strong>Filename: coord.csv</strong></p> <p>Names of the sampling locations and their geographic coordinates.</p> <ol> <li>Name - sampling locality identifier</li> <li>Lat - latitude</li> <li>Long - longitude</li> </ol> <p> </p> <p><strong>Filename: lineages.csv</strong></p> <ol> <li>id.sample - sample identifier</li> <li>host - host species (Arrela=<em>Arrhenantherum elatius</em>, Avesat=<em>Avena sativa</em>, Broine=<em>Bromus inermis</em>, Elyres=<em>Elymus repens</em>, Horvul=<em>Hordeum vulgaris</em>, Seccer=<em>Secale cereale</em>, Triaes=<em>Triticum aestivum</em>, Tririm=<em>Triticale rimpaui</em></li> <li>x, y - geodetic coordinates</li> <li>stems - no. of stems in a sample</li> <li>leaves - no. of leaves in a sample</li> <li>MT.01 to MT.27 - no. of mites belonging to each genetic lineage</li> </ol>
SMP01 Spatial variation of soil microbial processes under Cornus drummondii shrubs of varying size at Konza Prairie, 2017
Soil was collected from multiple locations under individual Cornus drummondii shrub islands of varying size to measure within-shrub heterogeneity in soil microbial processes. Soil chemistry (Total C, Total N, extractable inorganic N, extractable P, and organic matter cotent), microbial biomass C and N, and potential extracellular enzymatic activity of β-glucosidase, phosphatase, NAG-ase, and LAP-ase were measured. Potential carbon mineralization and the isotopic composition of respired soil carbon was measured over a 77-day laboratory incubation.
Object-based audio scene files for variations of the spatial arrangement in pop mixes for Wave Field Synthesis
<p>This entry contains object-based audio meta-data to generate the mixes published at http://dx.doi.org/10.5281/zenodo.61000.</p> <p>Have a look at README.md for further details.</p>
Microsatellite genotypes for «Genetic diversity and spatial genetic structure support the specialist‑generalist variation hypothesis in two sympatric woodpecker species»
<p>Species are often arranged along a continuum from “specialists” to “generalists”. Specialists typically use fewer resources, occur in more patchily distributed habitats and have overall smaller population sizes than generalists. Accordingly, the specialist-generalist variation hypothesis (SGVH) proposes that populations of habitat specialists have lower genetic diversity and are genetically more differentiated due to reduced gene flow compared to populations of generalists. Here, expectations of the SGVH were tested by examining genetic diversity, spatial genetic structure and contemporary gene flow in two sympatric woodpecker species differing in habitat specialization. Compared to the generalist great spotted woodpecker (<em>Dendrocopos major</em>), lower genetic diversity was found in the specialist middle spotted woodpecker (<em>Dendrocoptes medius</em>). Evidence for recent bottlenecks was revealed in some populations of the middle spotted woodpecker, but in none of the great spotted woodpecker. Substantial spatial genetic structure and a significant correlation between genetic and geographic distances were found in the middle spotted woodpecker, but only weak spatial genetic structure and no significant correlation between genetic and geographic distances in the great spotted woodpecker. Finally, estimated levels of contemporary gene flow did not differ between the two species. Results are consistent with all but one expectations of the SGVH. This study adds to the relatively few investigations addressing the SGVH in terrestrial vertebrates.</p>
Modeling biogeochemical responses of tundra ecosystems to temporal and spatial variations in climate in the Kuparuk River Basin , Alaska, 1921 to 2100.
Output data set of the MBL-GEM III model run for tussock tundra in the Kuparuk River Basin, Alaska, described in detail in Le Dizès, S., B. L. Kwiatkowski, E. B. Rastetter, A. Hope, J. E. Hobbie, D. Stow, and S. Daeschner, Modeling biogeochemical responses of tundra ecosystems to temporal and spatial variations in climate in the Kuparuk River Basin (Alaska), J. Geophys. Res., 108(D2), 8165, doi:10.1029/2001JD000960, 2003. We ran the model at a 10 km x 10 km resolution for 123 cells at a yearly time step for 180 years, from 1921 to 2100. Two scenarios enabled the investigation of the effects of two opposing climate change scenarios for the 2001-2100 future period: warmer and wetter ("wet scenario" or Scenario 1) and warmer and drier ("dry scenario" or Scenario 2). These 246 files contain all simulation results for each scenario for individual cells in the Kuparuk River basin.
Spatially corrected dataset for natural variation across Arabidopsis diversity panel in early responses to salt stress
<p>The spatially corrected data of Arabidopsis thaliana accessions, which were grown according to the established protocol for studying salt stress in soil experiment (described in detail here dx.doi.org/10.17504/protocols.io.4xzgxp6), in the PSI facility, Czech Republic.</p> <p>The spatial correction was done using the asreml package. The data was subsequently used for the Genome-Wide Association Study. </p>
Data from: Spatial and seasonal variation in thermal sensitivity within North American bird species
<p>Responses of wildlife to climate change are typically quantified at the species level, but physiological evidence suggests significant intraspecific variation in thermal sensitivity given adaptation to local environments and plasticity required to adjust to seasonal environments. Spatial and temporal variation in thermal responses may carry important implications for climate change vulnerability; for instance, sensitivity to extreme weather may increase in specific regions or seasons. Here, we leverage high-resolution observational data from eBird to understand regional and seasonal variation in thermal sensitivity for 20 bird species. Across their ranges, most birds demonstrated regional and seasonal variation in both thermal peak and range, or the temperature and range of temperatures of greatest occurrence. Some birds demonstrated constant thermal peaks or ranges across their geographic distributions and while others varied according to local and current environmental conditions. Across species, birds typically invested in either geographic or seasonal adaptation to climate. Local adaptation and phenotypic plasticity are likely important but neglected aspects of organismal responses to climate change.</p>
Data from: A species' response to spatial climatic variation does not predict its response to climate change
<p>The dominant paradigm for assessing ecological responses to climate change assumes that future states of individuals and populations can be predicted by current, species-wide performance variation across spatial climatic gradients. However, if the fates of ecological systems are better predicted by past responses to <em>in situ</em> climatic variation through time, this current analytical paradigm may be severely misleading. Empirically testing whether spatial or temporal climate responses better predict how species respond to climate change has been elusive, largely due to restrictive data requirements. Here we leverage a newly collected network of ponderosa pine tree-ring time series to test whether statistically inferred responses to spatial versus temporal climatic variation better predict how trees have responded to recent climate change. When compared to observed tree growth responses to climate change since 1980, predictions derived from spatial climatic variation were wrong in both magnitude and direction. This was not the case for predictions derived from climatic variation through time, which were able to replicate observed responses well. Future climate scenarios through the end of the 21st century exacerbated these disparities. These results suggest that the currently dominant paradigm of forecasting the ecological impacts of climate change based on spatial climatic variation may be severely misleading over decadal to centennial timescales.</p>
Fig. 3 in Spatial Variation Of The Land Snail Brephulopsis Cylindrica (Gastropoda, Pulmonata, Enidae): A Fractal Approach
Fig. 3. The dependence between intrapopulation variation (Mst) and the sample sites number in B. cylindrica: A — shell height (HS); B — shell width (WS); C — shell form index (FS) (95 % confidence interval is indicated by dotted lines).
Fig. 4 in Spatial Variation Of The Land Snail Brephulopsis Cylindrica (Gastropoda, Pulmonata, Enidae): A Fractal Approach
Fig. 4. Plots of the logarithms of semivariance versus logarithms of spatial scale (in meter) for morphometric shells traits of B. cylindrica of the studying population. D — fractal dimension value; R2 — determination coefF ficient): A — shell height (HS); B — shell width (WS); C — shell form index (FS).
Fig. 2 in Spatial Variation Of The Land Snail Brephulopsis Cylindrica (Gastropoda, Pulmonata, Enidae): A Fractal Approach
Fig. 2. Moran's index for morphometric shells traits of B. cylindrica of the studying population: A — shell height (HS); B — shell width (WS); C — shell form index (FS). Significant values of Moran's index indicated as solid circles.
Fig. 1 in Spatial Variation Of The Land Snail Brephulopsis Cylindrica (Gastropoda, Pulmonata, Enidae): A Fractal Approach
Fig. 1. The variation of morphometric shell traits in B. cylindrica from different sample sites: A — shell height (HS); B — shell width (WS); C — shell form index (FS).
Fig. 6 in Spatial variation of summer microphytoplankton and zooplankton communities related to environmental parameters in the coastal area of Djerba Island (Tunisia, Eastern Mediterranean) Abstract
Fig. 6: Spatial variation of copepod demographic class density: copepod nauplii, copepodit and adult males and females along the west and east coasts of Djerba Island.
Fig 8 in Spatial variation of summer microphytoplankton and zooplankton communities related to environmental parameters in the coastal area of Djerba Island (Tunisia, Eastern Mediterranean) Abstract
Fig 8: Correlation matrix (Pearson test) for biological variables in relation to abiotic variables determined along the west and east coasts of Djerba Island.
Fig. 4 in Spatial variation of summer microphytoplankton and zooplankton communities related to environmental parameters in the coastal area of Djerba Island (Tunisia, Eastern Mediterranean) Abstract
Fig. 4: Spatial variations of microphytoplankton abundance, microphytoplankton groups, dominant species, species richness and species diversity index along the west and east coasts of Djerba Island.
Fig. 7 in Spatial variation of summer microphytoplankton and zooplankton communities related to environmental parameters in the coastal area of Djerba Island (Tunisia, Eastern Mediterranean) Abstract
Fig. 7: Principal component analysis (PCA) (axis I and II) of microphytoplankton and zooplankton communities' abundance and selected environmental variables along the west and east coasts of Djerba Island.
Fig. 3 in Spatial variation of summer microphytoplankton and zooplankton communities related to environmental parameters in the coastal area of Djerba Island (Tunisia, Eastern Mediterranean) Abstract
Fig. 3: Spatial variations of nutrient concentrations: nitrite (NO -), nitrate (NO -), ammonium (NH +), total nitrogen (T- 2 3 4 N), orthophosphate (PO 3-), total phosphate (T-P), N/P ratio, 4 and silicate along the west and east coasts of Djerba Island.
Fig. 1 in Spatial variation of summer microphytoplankton and zooplankton communities related to environmental parameters in the coastal area of Djerba Island (Tunisia, Eastern Mediterranean) Abstract
Fig. 1: Location of sampling stations along the western and eastern coasts of Djerba Island. The grey contour lines in the maps show the position of the isobaths and the numbers in parenthesis indicate the depths of these isobaths. Table 1. Sampling date, depth, latitude and longitude of sampled stations.
Fig. 2 in Spatial Variation In Prey Composition And Its Possible Effect On Reproductive Success In An Expanding Eastern Imperial Eagle (Aquila Heliaca) Population
Fig. 2. Cluster analyses of imperial eagle breeding areas based on prey composition data. Region codes are presented in Fig. 1. Codes with bold characters represent mountainous habitats. The single breeding pair of the Cserehát Mountains was excluded from the analysis, because of low sample size
Fig. 3 in Spatial Variation In Prey Composition And Its Possible Effect On Reproductive Success In An Expanding Eastern Imperial Eagle (Aquila Heliaca) Population
Fig. 3. Frequency of the three main prey species (a-c) and reproductive success (d) of imperial eagles in two East-Hungarian regions. Boxplots presents the minimum-maximum (whiskers), lower and upper quartiles (box) and the median (line) of the data. Dots are outliers. Significance of difference is in-
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.