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877 results for “distribution modelling”

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A comparison among three ways to assemble wall-to-wall land-cover maps from distribution models of vegetation types

<p>Dataset accompanying manuscript <em>&quot;A comparison among three ways to assemble wall-to-wall land-cover maps from distribution models of vegetation types&quot;. </em>Datasets contain a wall-to-wall map of vegetation types covering the study area of terrestrial Norway, produced using three methods for assembling individual predictions from Distribution models (<em>probability-based method</em>, <em>performance-based method</em> and <em>prevalence-based method</em>).&nbsp;</p>

opencc-by-4.0Jun 2021View details →
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Model output, Khaled et al., Iron distribution in the aqueous phase (short title)

<p>Data for figures (Khaled et al., The number fraction of iron-containing particles affects OH, HO2 and H2O2 budgets in the atmospheric aqueous phase, Atmos. Chem. Phys.)</p>

opencc-by-4.0Jan 2022View details →
dryad40/100

Using species distribution models and decision tools to direct surveys and identify potential translocation sites for a critically endangered species

<p>Aim: Occurrence records for cryptic species are typically limited or highly uncertain, leaving their distributions poorly resolved and hampering conservation. This can apply to well‐studied species, and increased survey effort and/or novel methods are required to improve distribution data. Here, we paired species distribution modelling (SDM) with decision tools to direct surveys for the critically endangered Leadbeater's possum (Gymnobelideus leadbeateri) outside its current restricted range. We also assessed survey areas for their suitability to host translocations.</p> <p>Location: Victoria, Australia.</p> <p>Method: We used both recent and historic records (now out of range and spatially uncertain) of Leadbeater's possum to build SDMs using MaxEnt. The SDMs informed an initial multi‐criteria decision analysis (MCDA) that enabled prioritization of 80 survey sites across seven forest patches (13–145 km outside the known range), which we surveyed using camera traps. Site and vegetation data were used in a post‐survey MCDA to rank their potential translocation suitability.</p> <p>Results: The SDM predictions were consistent with the species' ecology, identifying cold areas with high rainfall that had not recently burnt as suitable. The spatial uncertainty of records did not exert a strong influence on either model predictions or the ranking of patches for surveys. Camera trap surveys yielded records of 19 native species, with Leadbeater's possum detected in only one survey patch, 13 km outside of its previously known range. The post‐survey MCDA identified three forest patches as potentially suitable for conservation translocations, and these priorities were not sensitive to the decision criteria used.</p> <p>Main conclusions: The approach outlined here prioritized survey effort over a large area, resulting in detection of Leadbeater's possum in one new patch. The potential translocation sites identified could present an important risk‐spreading measure for the species given the threat posed by bushfire. Combining SDMs and decision tools can help target surveys and guide subsequent conservation strategies.</p>

opencc-zeroJan 2022View details →
zenodo40/100

Fig. 2 in Associations Between Habitat Quality And Body Size In The Carpathian-Podolian Land Snail Vestia Turgida: Species Distribution Model Selection And Assessment Of Performance

Fig. 2. Linear relationship (solid line) and 95 % confidence interval (gray area) between habitat quality predicted by the BART model (x-axis) and shell height (H in millimeters, y-axis), derived from the linear mixed model.

opencc-by-4.0Jan 2021View details →
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Fig. 4. Partial dependence plot for topographic Fig. 5 in Associations Between Habitat Quality And Body Size In The Carpathian-Podolian Land Snail Vestia Turgida: Species Distribution Model Selection And Assessment Of Performance

Fig. 4. Partial dependence plot for topographic Fig. 5. Partial dependence plot for terrain roughness wetness index (TWI). index (tri).

opencc-by-4.0Dec 2021View details →
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Fig. 6 in Associations Between Habitat Quality And Body Size In The Carpathian-Podolian Land Snail Vestia Turgida: Species Distribution Model Selection And Assessment Of Performance

Fig. 6. Partial dependence plot for pH water (phh2o). Fig. 7. Partial dependence plot for silt content (SLT).

opencc-by-4.0Jan 2021View details →
dryad40/100

Habitats as predictors in species distribution models: Shall we use continuous or binary data?

<p>The representation of a land cover type (i.e., habitat) within an area is often used as an explanatory variable in species distribution models. However, it is possible that a simple binary presence/absence of the suitable habitat might be the most important determinant of the presence/absence of some species and, thus, be a better predictor of species occurrence than the continuous parameter (area). We hypothesize that the binary predictor is more suitable for relatively rare habitats (e.g., wetlands) while for common habitats (e.g., forests) the amount of the focal habitat is a better predictor. We used the Third Atlas of Breeding Birds in the Czech Republic as the source of species distribution data and CORINE Land Cover inventory as the source of the landcover information. To test our hypothesis, we fitted generalized linear models of 32 water and 32 forest bird species. Our results show that for water bird species, models using binary predictors (presence/absence of the habitat) performed better than models with continuous predictors (i.e., the amount of the habitat); for forest species, however, we observed the opposite. Thus, future studies using habitats as predictors of species occurrences should consider the prevalence of the habitat in the landscape, and the biological role of the habitat type in the particular species' life history. In addition, performing a preliminary comparison of the performance of the binary and continuous versions of habitat predictors (e.g., using information criteria) prior to modelling, during variable selection, can be beneficial. These are simple steps that will improve explanatory and predictive performance of models of species distributions in biogeography, community ecology, macroecology, and ecological conservation.</p>

opencc-zeroMar 2022View details →
zenodo40/100

Fig. 3. Partial dependence plot for BIO17 in Associations Between Habitat Quality And Body Size In The Carpathian-Podolian Land Snail Vestia Turgida: Species Distribution Model Selection And Assessment Of Performance

Fig. 3. Partial dependence plot for BIO17 = Precipitation of Driest Quarter; gray area = 95 % confidence interval.

opencc-by-4.0Jan 2021View details →
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Fig. 6 in Gis Modelling Of The Distribution Of Terrestrial Tortoise Species: Testudo Graeca And Testudo Hermanni (Testudines, Testudinidae) Of Eastern Europe In The Context Of Climate Change

Fig. 6. Result of the analysis of Binomial tests (CliMond 2090 (2081–2100)): A — T. graeca; B — T. hermanni.

opencc-by-4.0Dec 2021View details →
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Fig. 3 in Gis Modelling Of The Distribution Of Terrestrial Tortoise Species: Testudo Graeca And Testudo Hermanni (Testudines, Testudinidae) Of Eastern Europe In The Context Of Climate Change

Fig. 3. Niche clustering (Geographic space, CliMond 1975 (1970–2000)) from: A — T. graeca (1. T. g. ibera, 2. T. nikolskii, 3. T. g. anamurensis, 4. T. g. floweri, 5. T. g. antakyensis, 6. T. g. pallasi, 7. T. g. armenica, 8. T. g. perses, buxtoni, 9. T. g. terrestris); B — T. hermanni (1. T. h. hermanni, 2. T. h. hervegovinensis, 3. T. h. boettgeri), red circles showing the approximate ranges of subspecies according to "Turtles…, 2017" World" (2017).

opencc-by-4.0Dec 2021View details →
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Fig. 2 in Gis Modelling Of The Distribution Of Terrestrial Tortoise Species: Testudo Graeca And Testudo Hermanni (Testudines, Testudinidae) Of Eastern Europe In The Context Of Climate Change

Fig. 2. The "Ecological envelope" — relationship bio01 "Annual mean temperature", °C &amp; bio12 "Annual precipitation", mm (DivaGis): A — T. graeca; B — T. hermanni.

opencc-by-4.0Dec 2021View details →
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Fig. 5 in Gis Modelling Of The Distribution Of Terrestrial Tortoise Species: Testudo Graeca And Testudo Hermanni (Testudines, Testudinidae) Of Eastern Europe In The Context Of Climate Change

Fig. 5. Potential (probabilistic) model of T. hermanni world expansion built in the Maxent program based on the CliMond: A — 1975 (1970–2000); B — 2090 (2081–2100)) climatic data and GBIF data (2021). Areas of the highest habitat suitability (&gt; 0.3–0.5) are colored in red and areas of the lowest (&lt;0.2) — in blue (SAGA GIS).

opencc-by-4.0Dec 2021View details →
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Fig. 4 in Gis Modelling Of The Distribution Of Terrestrial Tortoise Species: Testudo Graeca And Testudo Hermanni (Testudines, Testudinidae) Of Eastern Europe In The Context Of Climate Change

Fig. 4. Potential (probabilistic) model of T. graeca expansion built in the Maxent program based on the CliMond: A — 1975 (1970–2000); B — 2090 (2081–2100)) climatic data and GBIF data (2021 a). Areas of the highest habitat suitability (&gt; 0.3–0.5) are colored in red and areas of the lowest (&lt;0.2) — in blue (SAGA GIS).

opencc-by-4.0Dec 2021View details →
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Fig. 5. The marginal response curve for the explanatory variable Bio14 in Modelling The Bioclimatic Niche And Distribution Of The Steppe Mouse, Mus Spicilegus (Rodentia, Muridae), In Ukraine

Fig. 5. The marginal response curve for the explanatory variable Bio14 (Precipitation of driest week). (HS — habitat suitability).

opencc-by-4.0Nov 2019View details →
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Fig. 1 in Modelling The Bioclimatic Niche And Distribution Of The Steppe Mouse, Mus Spicilegus (Rodentia, Muridae), In Ukraine

Fig. 1. Occurrences of Mus spicilegus in Ukraine and neighbouring areas used for creating the ENM. [Data collected before (triangles) and after (circles) 1990.]

opencc-by-4.0Nov 2019View details →
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Fig. 4. The marginal response curve for the explanatory variable Bio09 in Modelling The Bioclimatic Niche And Distribution Of The Steppe Mouse, Mus Spicilegus (Rodentia, Muridae), In Ukraine

Fig. 4. The marginal response curve for the explanatory variable Bio09 (Mean temperature of driest quarter). (HS — habitat suitability).

opencc-by-4.0Nov 2019View details →
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Fig. 7. 0.5 in Modelling The Bioclimatic Niche And Distribution Of The Steppe Mouse, Mus Spicilegus (Rodentia, Muridae), In Ukraine

Fig. 7. 0.5 oC isotherms for Bio09 (Mean temperature of driest quarter) for different time periods: 1 — 1980s; 2 — 2000s; 3 — contemporary; 4 — predicted for 2030.

opencc-by-4.0Nov 2019View details →
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Fig. 6. A in Modelling The Bioclimatic Niche And Distribution Of The Steppe Mouse, Mus Spicilegus (Rodentia, Muridae), In Ukraine

Fig. 6. A current climate habitat suitability map for the Steppe mouse (Mus spicilegus) in Ukraine. Darker shades of gray denote areas of higher predicted habitat suitability probabilities (≥ 0.5) and lighter shades correspond to lower (≥ 0.311 and &lt;0.5). [Administrative regions in Ukraine: 1 — Chernihiv Region; 2 — Kyiv Region; 3 — Ternopil Region; 4 — Ivano-Frankivsk Region.]

opencc-by-4.0Nov 2019View details →
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Fig. 1. The potential distribution map for B in Long-Term Bioclimatic Modelling The Distribution Of The Fire-Bellied Toad, Bombina Bombina (Anura, Bombinatoridae), Under The Influence Of Global Climate Change

Fig. 1. The potential distribution map for B. bombina under contemporary climatic conditions. The colour gradient represents high (red) to low (green) habitat suitability for the species.

opencc-by-4.0Jul 2018View details →
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Fig. 4. The potential distribution map for B. bombina under projected 2050 in Long-Term Bioclimatic Modelling The Distribution Of The Fire-Bellied Toad, Bombina Bombina (Anura, Bombinatoridae), Under The Influence Of Global Climate Change

Fig. 4. The potential distribution map for B. bombina under projected 2050 climatic conditions. The colour gradient represents high (red) to low (green) habitat suitability for the species.

opencc-by-4.0Jul 2018View 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