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338 results for “geographic range”

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zenodo40/100

Figure 1 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?

Figure 1. Map of Africa and Middle East showing collecting localities of Cc5, C. zastrowi and specimens closely resembling those taxa.

opencc-by-4.0Dec 2006View details →
zenodo40/100

Figure 7 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?

Figure 7. Dorsal view of left half of third-instar larval head capsules. (A)–(C) Cc5 from Eilat, Israel; (D) C. zastrowi from Cedarberg, South Africa. Head markings discussed in the text are labeled. In Cc5, the most common condition for head markings is shown in B.

opencc-by-4.0Dec 2006View details →
zenodo40/100

Figure 5 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?

Figure 5. Scatterplot of the first two factors of a principal components analysis of 19 song features (see text) of Cc5, C. zastrowi, C. lucasina, C. mediterranea and C. agilis. Each data point represents a single individual, coded by taxon.

opencc-by-4.0Dec 2006View details →
zenodo40/100

Text-fig. 13. Scatter diagram of m1 length vs SDQ for pre-Eemian (time slice 5) Arvicola samples from different geographical provenances compared with M. savini-A. mosbachensis and Arvicola sapidus. Empty dotted ovals indicate the range of extant Arvicola ex gr. amphibius samples from Italy (cyan) and from the other European locations (green) Abbreviations: FR – France, GE – Germany, IT – Italy, SP – Spain. in Independent Water Vole (Mimomys Savini, Arvicola: Rodentia, Mammalia) Lineages In Italy And Central Europe

Text-fig. 13. Scatter diagram of m1 length vs SDQ for pre-Eemian (time slice 5) Arvicola samples from different geographical provenances compared with M. savini-A. mosbachensis and Arvicola sapidus. Empty dotted ovals indicate the range of extant Arvicola ex gr. amphibius samples from Italy (cyan) and from the other European locations (green) Abbreviations: FR – France, GE – Germany, IT – Italy, SP – Spain.

opencc-by-4.0Nov 2020View details →
zenodo40/100

Text-fig. 11. Scatter diagram of m1 length vs SDQ for Würmian/Weichselian (time slice 3) Arvicola samples from different geographical provenances compared with M. savini-A. mosbachensis and extant Arvicola sapidus. Empty dotted ovals indicate the range of extant Arvicola ex gr. amphibius samples from Italy (cyan) and from the other European locations (green) Abbreviations: FR – France, GE – Germany, IT – Italy, SP – Spain. in Independent Water Vole (Mimomys Savini, Arvicola: Rodentia, Mammalia) Lineages In Italy And Central Europe

Text-fig. 11. Scatter diagram of m1 length vs SDQ for Würmian/Weichselian (time slice 3) Arvicola samples from different geographical provenances compared with M. savini-A. mosbachensis and extant Arvicola sapidus. Empty dotted ovals indicate the range of extant Arvicola ex gr. amphibius samples from Italy (cyan) and from the other European locations (green) Abbreviations: FR – France, GE – Germany, IT – Italy, SP – Spain.

opencc-by-4.0Nov 2020View details →
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Text-fig. 12. Scatter diagram of m1 length vs SDQ for Eemian (time slice 4) Arvicola samples from different geographical provenances compared with M. savini-A. mosbachensis and Arvicola sapidus. Empty dotted ovals indicate the range of extant Arvicola ex gr. amphibius samples from Italy (cyan) and from the other European locations (green) Abbreviations: FR – France, GE – Germany, IT – Italy, SP – Spain. in Independent Water Vole (Mimomys Savini, Arvicola: Rodentia, Mammalia) Lineages In Italy And Central Europe

Text-fig. 12. Scatter diagram of m1 length vs SDQ for Eemian (time slice 4) Arvicola samples from different geographical provenances compared with M. savini-A. mosbachensis and Arvicola sapidus. Empty dotted ovals indicate the range of extant Arvicola ex gr. amphibius samples from Italy (cyan) and from the other European locations (green) Abbreviations: FR – France, GE – Germany, IT – Italy, SP – Spain.

opencc-by-4.0Nov 2020View details →
zenodo40/100

WRF Geographic Files for Cordillera Mountain Range Precipitation Experiments

<p>These WRF geographic files (in netcdf format) were used as input for experiments to evaluate the sensitivity of Tropical Cyclone precipitation to the height of the Cordillera Mountain Range in Luzon, Philippines. A total of six files are included, for two domains (d01 and d02) and three different orographic experiments (orig, redu, enha).</p> <p>These are provided to allow reproduction of the said sensitivity experiments.</p>

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

A pathogen's spatial range is not constrained by geographical features in the flax rust pathosystem

<p>In this study, we performed several transect surveys over the course of the 2021 summer field season to assess potential ecogeographical range determinants for Lewis flax (<em>Linum</em> <em>lewisii</em>) and its pathogen, flax rust (<em>Melamspora</em> <em>lini</em>), in the area surrounding the Rocky Mountain Biological Laboratory in Gothic, Colorado. Additionally, we used generalized additive models to examine the effects of host population density and metapopulation structure on disease presence and prevalence.</p>

opencc-zeroSep 2023View details →
dryad40/100

Data from: The evolution of environmental tolerance and range size: A comparison of geographically restricted and widespread Mimulus

Open the record for dataset details and reuse information.

publicOct 2022View details →
dryad40/100

Older lineages of oribatid mites in mountain ranges have broader geographic ranges and exhibit more generalistic traits

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publicMar 2025View details →
dryad40/100

Rapid evolution of host repertoire and geographic range in a young and diverse genus of montane butterflies

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publicNov 2024View details →
dryad40/100

Data from: Fluctuation of ecological niches and geographic range shifts along chile pepper's domestication gradient

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publicDec 2023View details →
dryad40/100

A pathogen’s spatial range is not constrained by geographical features in the flax rust pathosystem

Open the record for dataset details and reuse information.

publicSep 2023View details →
dryad40/100

Diversification in the Rosales is influenced by dispersal, geographic range size, and pre-existing species richness

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publicApr 2022View details →
dryad40/100

EcoPhyloMapper: an R package for integrating geographic ranges, phylogeny, and morphology

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publicAug 2022View details →
dryad40/100

Data from: Phylogenetic biogeography inference using dynamic paleogeography models and explicit geographic ranges

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publicAug 2024View details →
dryad40/100

Geographic range shapes influence species richness in global hotspots

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publicJul 2025View details →
dryad40/100

Data from: Aridity drives coordinated trait shifts but not decreased trait variance across the geographic range of eight Australian trees

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publicAug 2020View details →
dryad36/100

Data from: Expressed mutational load increases towards the edge of a species' geographic range

There is no general explanation for why species have restricted geographic distributions. One hypothesis posits that range expansion or increasing scarcity of suitable habitat result in accumulation of mutational load due to enhanced genetic drift, which constrains population performance towards range limits and further expansion. We tested this hypothesis in the North American plant, Arabidopsis lyrata. We experimentally assessed mutational load by crossing plants of 20 populations from across the entire species range and by raising the offspring of within- and between-population crosses at five common garden sites within and beyond the range. Offspring performance was tracked over three growing seasons. The heterosis effect, depicting expressed mutational load, was increased in populations with heightened genomic estimates of load, longer expansion distance or long-term isolation, and a selfing mating system. The decline in performance of within-population crosses amounted to 80%. Mutation accumulation due to past range expansion and long-term isolation of populations in the area of range margins is therefore a strong determinant of population-mean performance, and the magnitude of effect may be sufficient to cause range limits.

opencc-zeroJul 2020View details →
dryad36/100

Data from: A resurrection study reveals limited evolution of thermal performance in response to recent climate change across the geographic range of the scarlet monkeyflower

<p>Evolutionary rescue can prevent populations from declining under climate change, and should be more likely at high-latitude, "leading" edges of species' ranges due to greater temperature anomalies and gene flow from warm-adapted populations. Using a resurrection study with seeds collected before and after a seven-year period of record warming, we tested for thermal adaptation in the scarlet monkeyflower <i>Mimulus</i> <i>cardinalis</i>. We grew ancestors and descendants from northern-edge, central, and southern-edge populations across eight temperatures. Despite recent climate anomalies, populations showed limited evolution of thermal performance curves. However, one southern population evolved a narrower thermal performance breadth by 1.31 °C, which matches the direction and magnitude of the average decrease in seasonality experienced. Consistent with the climate variability hypothesis, thermal performance breadth increased with temperature seasonality across the species' geographic range. Inconsistent with performance trade-offs between low and high temperatures across populations, we did not detect a positive relationship between thermal optimum and mean temperature. These findings fail to support the hypothesis that evolutionary response to climate change is greatest at the leading edge, and suggest that the evolution of thermal performance is unlikely to rescue most populations from the detrimental effects of rapidly changing climate.</p>

opencc-zeroJun 2020View 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