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645 results for “Spatial distributions”

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zenodo36/100

Fig. 2 in Spatial distribution of Culicidae (Diptera) larvae, and its implications for Public Health, in five areas of the Atlantic Forest biome, State of São Paulo, Brazil

Fig. 2. Spatial distribution of the species found in the Cruzeiro do Sul rural district.

opencc-by-4.0Jan 2017View details →
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Fig. 1 in Spatial distribution of Culicidae (Diptera) larvae, and its implications for Public Health, in five areas of the Atlantic Forest biome, State of São Paulo, Brazil

Fig. 1. Localization of the study areas in the Atlantic Forest biome, São Paulo state – Brazil.

opencc-by-4.0Jan 2017View details →
zenodo36/100

Fig. 6 in Spatial distribution of Culicidae (Diptera) larvae, and its implications for Public Health, in five areas of the Atlantic Forest biome, State of São Paulo, Brazil

Fig. 6. Adjusted Semi-variograms of the Simpson diversity index.

opencc-by-4.0Jan 2017View details →
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Fig. 3 in Spatial distribution of Culicidae (Diptera) larvae, and its implications for Public Health, in five areas of the Atlantic Forest biome, State of São Paulo, Brazil

Fig. 3. Spatial distribution of the species found in the Vale das Cigarras rural districts.

opencc-by-4.0Jan 2017View details →
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Figure 1 in First record of Aglais caschmirensis aesis (Fruhstorfer, 1912) (Lepidoptera: Rhopalocera: Nymphalidae) from Meghalaya, with a note on its spatial distribution

Figure 1. Aglais caschmirensis aesis (Fruhstorfer, 1912). a. Upperside. b. Underside.

opencc-by-4.0Dec 2019View details →
zenodo36/100

Fig. 1 in Distribution of carabid beetles in agroecosystems across spatial scales - A review

Fig. 1. Nested relations between the spatial levels (after Ettema, Wardle (2002), with changes).

opencc-by-4.0Dec 2008View details →
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Figure 2 in Spatial and temporal distribution of aquatic insects in the Dicle (Tigris) River Basin, Turkey, with new records

Figure 2. Psychomyia sp. larva: a- head, b- trochantin, c- anal claws.

opencc-by-4.0May 2016View details →
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Figure 1 in Spatial and temporal distribution of aquatic insects in the Dicle (Tigris) River Basin, Turkey, with new records

Figure 1. The locations of the selected sampling sites in the Tigris River Basin.

opencc-by-4.0May 2016View details →
zenodo36/100

Figure 1 in Spatial distribution of the epigeic species of earthworms Dendrobaena octaedra and D. attemsi (Oligochaeta: Lumbricidae) in the forest belt of the northwestern Caucasus

Figure 1. Locations of the earthworms of northwestern Caucasus.

opencc-by-4.0Jul 2019View details →
zenodo36/100

Figure 5 in Population structure and spatial distribution of the tiger (Panthera tigris, Felidae, Carnivora) in Southwestern Primorye (Russian Far East)

Figure 5. Layout of home ranges of the GPS-collared tigers (Hernandez-Blanco et al., 2015).

opencc-by-4.0Jun 2021View details →
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Figure 3 in Population structure and spatial distribution of the tiger (Panthera tigris, Felidae, Carnivora) in Southwestern Primorye (Russian Far East)

Figure 3. Relationship between tigers according to DNA identification.

opencc-by-4.0Jun 2021View details →
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Figure 2 in Population structure and spatial distribution of the tiger (Panthera tigris, Felidae, Carnivora) in Southwestern Primorye (Russian Far East)

Figure 2. Distribution of tiger tracks in Southwestern Primorye.

opencc-by-4.0Jun 2021View details →
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Fig. 1 in South American Sea Lions Otaria flavescens, a good indicator of relative spatial and temporal changes in the distribution and abundance of marine resources?

Fig. 1. Study area showing the location of the rookeries analysed at RÍo Negro Province, Argentina.

opencc-by-4.0Nov 2022View details →
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Spatial and seasonal distribution of selected nitrogen cycle genes in deep waters of the Baltic Proper

<p>The dataset provides information on nitrogen cycle related bins and gene characteristics across selected depths within the IDEAL, P1, and BY15 sites in the Baltic Sea. The dataset includes details such as gene spans, gene lengths, gene names, and the processes to which each gene is assigned. Additionally, it contains raw read counts, RPKM (reads per kilobase of transcript, per million mapped reads), family, phylum, bin, site, common bin identifiers for sites, and seasonal variations. Bin parameters, along with lineage-specific markers, are included to estimate the completeness of the bins. We focused on nitrogen loss processes (denitrification, anammox), reduction processes (dissimilatory nitrate reduction (DNR), dissimilatory nitrate reduction to ammonium (DNRA)), and oxidation (nitrification). <span>The reported results were obtained within the framework of the statutory activities of the Institute of Oceanology of the Polish Academy of Sciences and the following research project: 2019/34/E/ST10/00217 funded by the Polish National Science Centre.</span></p>

opencc-by-4.0Sep 2024View details →
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Characterizing the spatial correlation of coseismic slip distributions: A data driven Bayesian approach

<p>Slip models for the simulated case and the Illapel earthquake are provided. The zip file contains processed data, predictions, and uncertainty estimates for the Illapel event.</p>

opencc-by-4.0Oct 2024View details →
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Soil dissolved organic carbon in terrestrial ecosystems: global budget, spatial distribution and controls

<p><strong>Aims: </strong>Soil dissolved organic carbon (DOC) is a primary form of labile carbon in terrestrial ecosystems and therefore plays a vital role in soil carbon cycling. This study aims to quantify the budgets of soil DOC at biome- and global levels and to examine the variations in soil DOC and their environmental controls. Location: Global Time period: 1981 - 2019 Method: We compiled a global dataset and analyzed the concentration and distribution of DOC across 10 biomes.</p> <p><strong>Results: </strong>Large variations in DOC are found among biomes across space and the soil DOC concentration declines exponentially along soil depths. Tundra has the highest soil DOC concentration in 0 - 30 cm soils (453.75 (95% confidence interval: 324.95 – 633.5) mg·kg-1); whereas tropical and temperate forests have relatively lower DOC concentrations, ranging from 30.20 (24.78 - 36.80) mg·kg-1 to 54.54 (49.77 – 59.77) mg·kg-1. DOC generally accounts for &lt; 1% of total organic carbon in soils, and DOC in 0 - 30 cm contributes more than half of total DOC in 0 - 100 cm soil profile. Furthermore, variations in DOC are primarily controlled by soil texture, moisture, and total organic carbon.</p> <p><strong>Main conclusion: </strong>A global synthesis is combined with an empirical model to extrapolate the DOC concentration along soil profiles across the globe, and global budgets of DOC are estimated as 7.20 Pg C in top 0 - 30 cm and 12.97 Pg C in 0 - 100 cm, respectively, with a considerable variation among biomes. The strong soil texture control but weak TOC control on DOC variations suggest that the investigation of physical protection of soil organic carbon might need to expand to consider the labile C in soils. The global maps of DOC concentration serve as a benchmark for validating land surface models in estimating carbon storage in soils.</p>

opencc-zeroAug 2021View details →
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Spatial slip rate distribution along the SE Xianshuihe fault, eastern Tibet, and earthquake hazard assessment

<p><strong><em>Table 2:&nbsp;</em></strong><em><sup>10</sup></em><em>Be surface-exposure ages of Zheduotang (ZDT) and Moxi (MX) sites of the SE Xianshuihe fault.</em></p>

opencc-by-4.0Jul 2021View details →
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Energy-water and seasonal variations in climate underlie the spatial distribution patterns of gymnosperms species richness in China

<p>Studying the pattern of species richness is crucial in understanding the diversity and distribution of organisms in the earth. Climate and human influences are the major driving factors that directly influence the large-scale distributions of plant species, including gymnosperms. Understanding how gymnosperms respond to climate, topography, and human-induced changes is useful in predicting the impacts of global change. Here, we attempt to evaluate how climatic and human-induced processes could affect the spatial richness patterns of gymnosperms in China. Initially, we divided a map of the country into grid cells of 50 × 50 km<sup>2 </sup>spatial resolution and plotted the geographical coordinate distribution occurrence of 236 native gymnosperm taxa. The gymnosperm taxa were separated into three response variables: (i) all species, (ii) endemic species, and (iii) non-endemic species, based on their distribution. The species richness patterns of these response variables to four predictor sets were also evaluated: (i) energy-water, (ii) climatic seasonality, (iii) habitat heterogeneity, and (iv) human influences. We performed generalized linear models (GLMs) and variation partitioning analyses to determine the effect of predictors on spatial richness patterns. The results showed that the distribution pattern of species richness was highest in the southwestern mountainous area and Taiwan in China. We found a significant relationship between the predictor variable set and species richness pattern. Further, our findings provide evidence that climatic seasonality is the most important factor in explaining distinct fractions of variations in the species richness patterns of all studied response variables. Moreover, it was found that energy-water was the best predictor set to determine the richness pattern of all species and endemic species, while habitat-heterogeneity has a better influence on non-endemic species. Therefore, we conclude that with the current climate fluctuations as a result of climate change and increasing human activities, gymnosperms might face a high risk of extinction.</p>

opencc-zeroAug 2021View details →
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Fig. 6 in Spatial Distribution Of Tropical Estuarine Nematode Communities In Sarawak, Malaysia (Borneo)

Fig. 6. Percentage of contribution of each functional feeding group

opencc-by-4.0Feb 2012View details →
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Fig. 5. a in Spatial Distribution Of Tropical Estuarine Nematode Communities In Sarawak, Malaysia (Borneo)

Fig. 5. a, Two-dimensional MDS ordination constructed from the

opencc-by-4.0Feb 2012View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record