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1,514 results for “Widespread”
Data from: Repeated alpine flight loss within the widespread New Zealand stonefly Nesoperla fulvescens
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Data from: Rapid diversification of the Variable Seedeater superspecies complex despite widespread gene flow
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Data from: Widespread dysregulation of long non-coding genes associated with fatty acid metabolism, cell division, and immune response gene networks in xenobiotic-exposed rat liver
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Phylogeography and genetic diversity of the widespread katydid Ducetia japonica (Thunberg, 1815) across China
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Digital biodiversity datasets reveal breeding phenology and its drivers in a widespread North American mammal
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Data for: Widespread wood placement and regrading drive lateral connectivity and reworking of the channel and floodplain in a valley bottom reset to stage 0
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Male-like female morphs in hummingbirds: the evolution of a widespread sex-limited plumage polymorphism
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Data for: Phylogeography and populations genetics of a widespread cold-adapted ant, Prenolepis imparis
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An ancient and eroded social supergene is widespread across Formica ants
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Data for: Longitudinal metatranscriptomic sequencing of Southern California wastewater representing 16 million people from August 2020-21 reveals widespread transcription of antibiotic resistance genes
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Satellite-Based Estimates Reveal Widespread Forest Degradation in the Amazon
<p>This is the initial release of the repository containing the data used in the Global Change Biology article "Satellite-Based Estimates Reveal Widespread Forest Degradation in the Amazon" By Eric L Bullock, Curtis E. Woodcock, Carlos Souza Jr., and Pontus Olofsson. The github repository address is https://github.com/bullocke/amazon. </p>
Fig. 2 in The Leiobunum rupestre species group: resolving the taxonomy of four widespread European taxa (Opiliones: Sclerosomatidae)
Fig. 2. Distribution of the species of the Leiobunum rupestre species group. Red squares = L. rupestre Herbst, 1799; blue circles = L. gracile Thorell, 1876; green triangles = L. apenninicum (Martens, 1969); stippled line circumscribes area of L. subalpinum Komposch, 1998. Type localities are indicated by abbreviated taxon names (ape = apenninicum; gla = glabrum; gra = gracile; lae = laeve; nor = norvegicum; rup = rupestre; sub subalpinum; tis = tisciae). Arrows indicate a specified locality, if unprecisely given, the general area is indicated (rupestre = Saxony; gracile, laeve = Scania).
Flowering phenology of a widespread perennial herb shows contrasting responses to global warming between humid and non-humid regions
<p>The phenology data in paper published in Functional Ecology by Song et al. 2020, titled Flowering phenology of a widespread perennial herb shows contrasting responses to global warming between humid and non-humid regions</p>
Data from: Paleoclimatic evolution as the main driver of current genomic diversity in the widespread and polymorphic Neotropical songbird Arremon taciturnus
Several factors have been proposed as drivers of species diversification in the Neotropics, including environmental heterogeneity, the development of drainage systems and historical changes in forest distribution due to climatic oscillations. Here, we investigate which drivers contributed to the evolutionary history and current patterns of diversity of a polymorphic songbird (Arremon taciturnus) that is widely distributed in Amazonian and Atlantic forests as well as in Cerrado gallery and seasonally-dry forests. We use genomic, phenotypic and habitat heterogeneity data coupled with climatic niche modeling. Results suggest the evolutionary history of the species is mainly related to paleoclimatic changes, although changes in the strength of the Amazon river as a barrier to dispersal, current habitat heterogeneity and geographic distance were also relevant. We propose an ancestral distribution in the Guyana Shield, and recent colonization of areas south of the Amazon river at ~380–166 kya, expansion of distribution to southern Amazonia, Cerrado and the Atlantic Forest. Since then, populations south of the Amazon River have been subjected to cycles of isolation and possibly secondary contact due to climatic changes that affected habitat heterogeneity and population connectivity. Most Amazonian rivers are not associated to long lasting isolation of populations, but some might act as secondary barriers, susceptible to crossing under specific climatic conditions. Morphological variation, while stable in some parts of the distribution, is not a reliable indicator of genetic structure or phylogenetic relationships.
Fig. 21. A in Widespread polytypic species or complexes of local species? Revising bumblebees of the subgenus Melanobombus world-wide (Hymenoptera, Apidae, Bombus)
Fig. 21. A sample of 10 000 species trees from among 100 million trees for species of the subgenus Melanobombus von Dalla Torre, 1880 reconstructed with *BEAST from gene trees for the COI, 16S, opsin and PEPCK genes, displayed in green using Densitree, with the summary 'root canal' superimposed as a thick blue line. The outgroup B. nobilis Friese, 1905 is shown.
Fig. 11 in Widespread polytypic species or complexes of local species? Revising bumblebees of the subgenus Melanobombus world-wide (Hymenoptera, Apidae, Bombus)
Fig. 11. Numbers of unique COI haplotypes represented per species (y-axis, log scale) plotted against range size per species (x-axis, log scale). Unique COI haplotypes are listed in Fig. 10 and range size is measured as the number of large equal-area grid cells (611 000 km²) with records (Williams 1998).
Figs 139–180 in Widespread polytypic species or complexes of local species? Revising bumblebees of the subgenus Melanobombus world-wide (Hymenoptera, Apidae, Bombus)
Figs 139–180. Simplified diagrams for the colour patterns of the hair on the dorsum for the species from the integrative analysis. The dorsum is divided into regions, each of which shows only the predominant or most apparent colour for that region using a simplified colour palette, with olive indicating a mixture of black and yellow hair, and grey indicating a mixture of black and white hair. The keriensis-group. 139. Queen, China-Sichuan. 140. Worker, China-Sichuan. 141. Queen, China-Sichuan. 142. Queen, China-Sichuan. 143. Worker, China-Xizang. 144. Queen, India-Kashmir. 145. Male, China-Qinghai. 146. Male, India-Kashmir. 147. Male, China-Gansu. 148. Queen, Armenia. 149. Queen, Iran. 150. Male, Georgia. 151. Worker, China-Qinghai. 152. Male, China-Qinghai. 153. Queen, Mongolia. 154. Worker, Mongolia. 155. Male, Mongolia. 156. Male, Mongolia. 157. Queen, China-Sichuan. 158. Worker, China-Qinghai. 159. Worker, China-Qinghai. 160. Male, China-Qinghai. 161. Male, China-Qinghai. 162. Male, China-Qinghai. 163. Queen, Pakistan. 164. Queen, Pakistan. 165. Queen, Pakistan. 166. Queen, Pakistan. 167. Queen, Afghanistan. 168. Queen, Pakistan. 169. Queen, Pakistan. 170. Queen, India-Kashmir. 171. Male, India-Kashmir. 172. Male, India-Kashmir. 173. Queen, ChinaXinjiang. 174. Queen, Kyrgyzstan. 175. Queen, Kyrgyzstan. 176. Queen, Mongolia. 177. Queen, IndiaKashmir. 178. Male, Kazakhstan. 179. Male, China-Xinjiang. 180. Male, Mongolia.
Fig. 7. Sample sites for barcodes for the subgenus Melanobombus von Dalla Torre, 1880 in Widespread polytypic species or complexes of local species? Revising bumblebees of the subgenus Melanobombus world-wide (Hymenoptera, Apidae, Bombus)
Fig. 7. Sample sites for barcodes for the subgenus Melanobombus von Dalla Torre, 1880, colour-coded for the order in which the samples of selected barcoded individuals were added to the analyses, from blue (2011) to red (2019) (specimens may be much older). Spherical projection with the North Pole shown as a star, international boundaries as recognized by the UN shown as grey lines. Map projected in ArcGIS using the World_Shaded_Relief basemap © 2014 ESRI.
Figs 1‒6 in Widespread polytypic species or complexes of local species? Revising bumblebees of the subgenus Melanobombus world-wide (Hymenoptera, Apidae, Bombus)
Figs 1‒6. Individuals of the subgenus Melanobombus von Dalla Torre, 1880 (with photo credits). 1. Bombus eximius Smith, 1852, queen, Thailand (CT). 2. B. simillimus Smith, 1852, worker, IndiaKashmir (RR). 3. B. prshewalskyi Morawitz, 1880, worker, China-Gansu (PW). 4. B. eriophorus Klug, 1807, queen, Georgia (I. Popov). 5. B. semenovianus (Skorikov, 1914), male, India-Kashmir (PW). 6. B. ladakhensis Richards, 1928, male, China-Gansu (PW). Some images reversed.
Fig. 10. October 2019 in Widespread polytypic species or complexes of local species? Revising bumblebees of the subgenus Melanobombus world-wide (Hymenoptera, Apidae, Bombus)
Fig. 10. October 2019 (Fig. 8) Bayesian PTP analysis of MrBayes tree of unique COI barcodes (UHFPTP). Symbols as in Fig. 9.
ScienceDex guides
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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.