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487 results for “population differences”

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edi56/100

CBP01 Variable distance line-transect sampling of bird population numbers in different habitats on Konza Prairie

Records of bird species based on line transect sampling, giving perpendicular distance of sighting from the transect line on 16 separate transects. Bird surveys were conducted 2-4 times per year in January, April, June, and October for a 29-year period from 1981 to 2009. Transects were designed to determine bird communities and population numbers associated with tallgrass prairie habitats with different experimental treatments (fire frequency, grazed by bison vs. ungrazed), riparian habitats on forest edge, and gallery forests dominated by oak woodland.

openCC0Oct 2025View details →
zenodo48/100

Population genomics reveals differences in genetic structure between two endemic arboreal rodent species in threatened cloud forest habitat

<p>SNPs obtained by UNEAK pipeline for <em>Habromys schmidlyi </em>and <em>Reithrodontomys microdon</em>.&nbsp;</p> <p>Pleae cite as:&nbsp;</p> <p>Colunga-Salas P.,&nbsp;T Marines-Mac&iacute;as,&nbsp;G Hern&aacute;ndez-Canchola,&nbsp;S&nbsp;Barbosa,&nbsp;C&nbsp;Ram&iacute;rez,&nbsp;JB&nbsp;Searle,&nbsp;L&nbsp;Le&oacute;n-Paniagua. 2022.&nbsp;<strong>Population genomics reveals differences in genetic structure between two endemic arboreal rodent species in threatened cloud forest habitat</strong>. Mammalian Reasearch. Doi: 10.1007/s13364-022-00667-x</p>

opencc-by-4.0Jun 2022View details →
edi48/100

Monitoring of Microtus ochrogaster and Microtus pennsylvanicus populations in three different habitats in east-central Illinois, 1972 to 1997.

Populations of 2 species of arvicoline rodents, the prairie vole (Microtus ochrogaster) and meadow vole (Microtus pennsylvanicus), were monitored monthly from 1972-1997 in three distinct habitats: restored tallgrass prairie, bluegrass (Poa pratensis) and alfalfa (Medicago sativa). The study sites were located in the University of Illinois Biological Research Area (Phillips Tract) and Trelease Prairie. Tallgrass prairie was the original habitat of both species in Illinois. Bluegrass, an introduced species, represents the more common habitat in which the two species can be found today in Illinois. Alfalfa, an atypical habitat, provides an abundant source of high-quality food for both species. At each station, one wooden multiple-capture live-trap was placed. Every month, a two-day period of prebaiting was followed by a 3-day trapping session. The data include the species, individual identification, grid station, sex, reproductive status and body mass. Over the span of 25 years, three trapping sessions monthly were conducted to cover the three habitats, dedicating three weeks each month. Several papers have been based on these data.

openCC (other)Aug 2024View details →
edi48/100

CBP01 Variable distance line-transect sampling of bird population numbers in different habitats on Konza Prairie (Reformatted to the ecocomDP Design Pattern)

This data package is formatted as an ecocomDP (Ecological Community Data Pattern). For more information on ecocomDP see https://github.com/EDIorg/ecocomDP. This Level 1 data package was derived from the Level 0 data package found here: https://pasta.lternet.edu/package/metadata/eml/knb-lter-knz/26/11. The abstract below was extracted from the Level 0 data package and is included for context: Records of bird species based on line transect sampling, giving perpendicular distance of sighting from the transect line on 16 separate transects. Bird surveys were conducted 2-4 times per year in January, April, June, and October for a 29-year period from 1981 to 2009. Transects were designed to determine bird communities and population numbers associated with tallgrass prairie habitats with different experimental treatments (fire frequency, grazed by bison vs. ungrazed), riparian habitats on forest edge, and gallery forests dominated by oak woodland.

openCC0Jul 2021View details →
zenodo44/100

Data and code for 'Age structure of amphibian populations with endemic chytridiomycosis, across climatic regions with markedly different infection risk'

<p>This repository provides all data and R code from the analysis presented in the following paper:</p> <p>Turner, A., Heard, G., Hall, A., Wassens, S. (in review).&nbsp;Age structure of amphibian populations with endemic chytridiomycosis, across climatic regions with markedly different infection risk.</p> <p>The data are provided as a series of .csv files, R script and two zip folders of R packages (Surv_mod and VB_mod)</p> <p>1. <strong>Skeleto_dat_ready_Jan2021.csv</strong> Data from frog surveys conducted by Anna Turner</p> <p>2. <strong>Geoffs_data.csv</strong> Data from frog surveys conducted by Geoff Heard</p> <p>3. <strong>Environmental_variables_skeleto.csv</strong> Environmental data collected during surveys&nbsp;</p> <p>4. <strong>sk.dat_July21.csv</strong> Collated data from Anna and Geoff - created by &#39;Data_collation_for_analysis_2.R&#39; ready for analysis</p> <p>5.&nbsp;<strong>Variables_that_are_highly_correlated_with_each_other_season_wide.csv</strong> Testing for correlation</p> <p>6. <strong>Model_structure_skeleto_2.csv </strong>creates&nbsp;model structure for analysis</p> <p>7.&nbsp;<strong>Model_selection_statistics_June_21.csv&nbsp;</strong>Output from model</p> <p>R code is provided seperately for each of the following components:</p> <p>1. <strong>Data_collation_for_analysis_2.R</strong> Collating data from Anna and Geoffs datasets</p> <p>2. <strong>Skeleto_analysis_5.R - </strong>First uses regression modelling to explore factors correlated with variation in age</p> <p>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;- Following Scheele et al. (2016) regression models with a poisson distribution</p> <p>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;- Use bayesian non-linear regression to fit the Von Bertalanffy growth model to size-at-age data</p> <p>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;- Plots male and female growth curves</p> <p>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;- Uses catch curve approach to estimate survival from best fitting regression model following Scroggie&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;(2012) but with bayesian implementation</p>

opencc-by-4.0Jan 2022View details →
zenodo44/100

The geographic scale of population level variation in growth and nodulation differs for two species of the prairie clover

<p>Zenodo deposit for Pozzi et al (2024) AJB</p> <p>The geographic scale of population level variation in growth and nodulation differs for two species of the prairie clover</p> <p><strong>&nbsp;_____________________________________________________________________________________________________________________________________</strong></p> <p><strong>The geographic scale of population level variation in growth and nodulation differs for two species of the prairie clover</strong></p> <p>Adrien C.M. Pozzi<sup>1,2</sup>, Ruth G. Shaw<sup>1</sup>, Georgiana May<sup>1,3</sup></p> <p><sup>1</sup> Department of Ecology, Evolution and Behavior, University of Minnesota Twin-Cities, St Paul, MN 55108. <sup>2</sup> Current affiliation: Universite Claude Bernard Lyon 1, Laboratoire d'Ecologie Microbienne, UMR CNRS 5557, UMR INRAE 1418, VetAgro Sup, 69622 Villeurbanne, France. ORCID: 0000-0001-6765-4293. <sup>3</sup> Correspondence: Georgiana May (gmay@umn.edu)</p> <p><em><strong>Keywords:</strong></em></p> <p>conservation; <em>Dalea</em> spp.; habitat fragmentation; mutualism; nitrogen-fixing symbiosis; population level variation; native prairie legume; restoration; rhizobia</p> <p><em><strong>Description:</strong></em></p> <p>This Zenodo deposit is part of the MN LCCMR Healthy Prairies project granted to R. Shaw and G. May, UMN Twin-Cities. It contains the following files:</p> <p><span><span>&middot;<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span></span>&ldquo;Metadata &amp; data&rdquo; spreadsheet. <em>Contains metadata and data about the Twin Valley experiment (including the position of plants, an intermediary census, growth and nodulation traits for harvested plants, data on bacterial isolates from root nodules, and source modifiers for GenBank accessions OQ732394-OQ732572).</em></p> <p><span><span>&middot;<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span></span>&ldquo;Blast alignments output.txt&rdquo; text file. <em>Contains ouput of Blastn alignements for the 16S rRNA genes of bacterial isolates against the rRNA_typestrains/16S_ribosomal_RNA 16S ribosomal RNA (Bacteria and Archaea type strains) database, to determine the genus as recommended by GenBank during sequence submission.</em></p> <p><span><span>&middot;<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span></span>&ldquo;General script.R&rdquo;. <em>R script of the general statistical analyses produced for publication.</em></p> <p><span><span>&middot;<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span></span>&ldquo;General environment.RData&rdquo;.<em> The companion RData (environment) of the above R script.</em></p> <p><span><span>&middot;<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span></span>&ldquo;Trait model script.R&rdquo;. <em>R script of the plant trait models produced for publication</em></p> <p><span><span>&middot;<span>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span></span>&ldquo;Trait model environment.RData&rdquo;. <em>The companion RData (environment) of the above R script.</em></p> <p><strong><em>Acknowledgments:</em></strong></p> <p>The authors thank members of the May Lab (Mai Beauclaire, Em Daily, Mara Demers, Kane Keller, Cedric Ndinga-Muniania, Liam Vertal, Monica Watson) for their help in field and lab work. We thank members of the Healthy Prairies project (Shelby Flint, Anna Peschel, Bill Peterson) who provided much of the infrastructure that made this project possible, as well as help in setting up field experiments. We also thank volunteer undergrads from University of Minnesota Morris (Amelia Nelson, Emily Job, Lily Fulton) for assistance in measuring harvested plants and counting nodules. Funding for this project was provided by the Minnesota Environment and Natural Resources Trust Fund as recommended by the Legislative-Citizen Commission on Minnesota Resources (LCCMR) Project 00086965, Healthy Prairies.</p> <p>&nbsp;</p>

opencc-by-4.0Sep 2024View details →
zenodo44/100

Genome-wide characterization of human minisatellite VNTRs: population-specific alleles and gene expression differences

<p>This repository consists of minisatellite VNTR genotypes for 2,800 samples (2,770 individuals). The raw VCF files were produced using <a href="https://github.com/yzhernand/VNTRseek">VNTRseek</a>&nbsp;on xxx data sources: <a href="http://ftp.1000genomes.ebi.ac.uk/vol1/ftp/data_collections/1000_genomes_project/">30 high coverage WGS datasets</a>&nbsp;from the 1000 Genomes Project phase 3, <a href="https://www.internationalgenome.org/data-portal/data-collection/30x-grch38">2,504 unrelated genomes</a> from New York Genome Center (NYGC), <a href="https://www.internationalgenome.org/data-portal/data-collection/sgdp">253 genomes from Simons Diversity Genome Project</a>&nbsp;(SGDP), <a href="https://www.illumina.com/products/by-type/informatics-products/basespace-sequence-hub/apps/tumor-normal.html">two tumor-normal breast cancer samples</a>&nbsp;from Illumina Basespace, haploid genomes <a href="https://www.ncbi.nlm.nih.gov/sra/SRX652547">CHM1 </a>and <a href="https://www.ncbi.nlm.nih.gov/sra/SRX1009644">CHM13</a>, and seven genomes from the Personal Genome Project from the Genome In A Bottle Consortium (GIAB). Raw VCF files are provided for each data source separately.</p> <p>The raw VCF files were preprocessed (preprocess.sh) to extract genotypes and provided in VNTRseek_preprocessed_data.tar.gz (uncompressed size 10G). The R Markdown code to analyze the preprocessed data and produce figures and tables is also provided (tables_and_figures.Rmd). For more information see the ReadMe file.</p> <p>This work was supported in part by NSF grants IIS-1423022 and DBI-1559829.</p>

opencc-by-4.0Nov 2020View details →
edi44/100

Growth, development, activity, and survival of wood frog tadpoles from different populations in eastern NY in 2022.

These data were collected as two lab experiments that examined larval (i.e., tadpole) wood frog populations. The first was a time-to-death experiment in which we exposed individuals tadpoles to either a control or lethal concentrations of NaCl. The second was a growth and development experiment in which we raised tadpoles from the same populations in a sublethal concentration of NaCl for several weeks to examine their growth and development (i.e. Gosner developmental stage).

openCC (other)Mar 2024View details →
edi44/100

Relyea, R. A. 2002. Local population differences in phenotypic plasticity: Predator-induced changes in wood frog tadpoles. Ecological Monographs 72:77-93

Taxa that are divided into separate populations with low levels of interpopulation dispersal have the potential to evolve genetically based differences in their phenotypes and the plasticity of those phenotypes. These differences can be due to random processes, including genetic drift and founder effects, or they can be the result of different selection pressures among populations. I investigated population-level differences in predator- induced phenotypic plasticity in eight populations of larval wood frogs (Rana sylvatica) over a small geographic scale (interpopulation distances of 0.3–8 km). Using a common-garden experiment containing predator and no-predator environments, I found population differences in behavior, morphology, and life history. These responses exhibited a habitat-related pattern: the four populations from closed-canopy ponds did not differ from each other in any of their phenotypes whereas the four populations from opencanopy ponds did differ from each other in these traits. This phenotypic pattern matches the pattern of competitors and predators found in these two types of ponds. Based on two years of pond surveys, the four closed-canopy ponds contained very similar competitor and predator assemblages while the assemblages of the four open-canopy ponds were more diverse and highly variable among open-canopy ponds. When combined with past studies, which demonstrate that predators and competitors select for alternative behavioral and morphological traits, these patterns suggest that the population differences may have arisen via natural selection and not via random mutation or drift. In a second experiment, I cross-transplanted two of the populations into each other’s ponds to determine if the populations were locally adapted to the conditions of their native pond (using low and high competition crossed with the presence or absence of a lethal predator). The populations continued to exhibit phenotypic differences, and one of the two populations t

openCC (other)Jun 2024View details →
edi44/100

Blarina brevicauda populations in three different habitats in east-central Illinois, 1972 to 1997.

The population demography of the northern short-tailed shrew, Blarina brevicauda, was monitored monthly from 1972-1997 in bluegrass, alfalfa, and tallgrass prairie habitats in east-central Illinois. Blarina brevicauda were incidentally collected as part of a 25-year prairie vole (Microtus ochrogaster) and meadow vole (M. pennsylvanicus) trapping study. The study sites were located in the University of Illinois Biological Research Area (Phillips Tract) and Trelease Prairie. Animals were trapped with wooden multiple-capture live-traps. Over the span of 25 years, three 3-day trapping sessions monthly were conducted to cover the three habitats. All live shrews were toe-clipped at first capture for individual identification. Animals known to be present on study site, but not captured, were included in totals for that month. While trap mortality of shrews was high in this study (40%), the data obtained were sufficient for analysis of many aspects of the demography of the species.

openCC (other)Aug 2024View details →
edi44/100

CBP01 Variable distance line-transect sampling of bird population numbers in different habitats on Konza Prairie (Reformatted to a Darwin Core Archive)

This data package is formatted as a Darwin Core Archive (DwC-A, event core). For more information on Darwin Core see https://www.tdwg.org/standards/dwc/. This Level 2 data package was derived from the Level 1 data package found here: https://pasta.lternet.edu/package/metadata/eml/edi/339/2, which was derived from the Level 0 data package found here: https://pasta.lternet.edu/package/metadata/eml/knb-lter-knz/26/11. The abstract below was extracted from the Level 0 data package and is included for context: Records of bird species based on line transect sampling, giving perpendicular distance of sighting from the transect line on 16 separate transects. Bird surveys were conducted 2-4 times per year in January, April, June, and October for a 29-year period from 1981 to 2009. Transects were designed to determine bird communities and population numbers associated with tallgrass prairie habitats with different experimental treatments (fire frequency, grazed by bison vs. ungrazed), riparian habitats on forest edge, and gallery forests dominated by oak woodland.

openCC0Jul 2021View details →
dryad40/100

Genomic analyses of phenotypic differences between native and invasive populations of diffuse knapweed (Centaurea diffusa)

<p>Invasive species represent excellent opportunities to study the evolutionary potential of traits important to success in novel environments. Although some ecologically-important traits have been identified in invasive species, little is typically known about the genetic mechanisms that underlie invasion success in non-model species. Here, we use a genome-wide association (GWAS) approach to identify the genetic basis of trait variation in the non-model, invasive, diffuse knapweed (<i>Centaurea diffusa </i>Lam.<i> </i>[Asteraceae]). To assist with this analysis, we have assembled the first draft genome reference and fully annotated plastome assembly for this species, and the one of the first from this large, weedy, genus, which is of major ecological and economic importance. We collected phenotype data from 372 individuals from four native and four invasive populations of <i>C. diffusa </i>grown in a common environment. Using these individuals, we produced reduced-representation genotype-by-sequencing (GBS) libraries and identified 7058 SNPs. We identify two SNPs associated with leaf width in these populations, a trait which significantly varies between native and invasive populations. In this rosette forming species, increased leaf width is a major component of increased biomass, a common trait in invasive plants correlated with increased fitness. Finally, we use annotations from <i>Arabidopsis thaliana</i> to identify 98 candidate genes that are near the associated SNPs and highlight several good candidates for leaf width variation.</p>

opencc-zeroDec 2019View details →
dryad40/100

Data from: Different genetic structures revealed resident populations of a specialist parasitoid wasp in contrast to its migratory host

Genetic comparisons of parasitoids and their hosts are expected to reflect ecological and evolutionary processes that influence the interactions between species. The parasitoid wasp, Cotesia vestalis, and its host diamondback moth (DBM), Plutella xylostella, provide opportunities to test whether the specialist natural enemy migrates seasonally with its host or occurs as resident population. We genotyped 17 microsatellite loci and two mitochondrial genes for 158 female adults of C. vestalis collected from 12 geographical populations, as well as nine microsatellite loci for 127 DBM larvae from six separate sites. The samplings covered both the likely source (southern) and immigrant (northern) areas of DBM from China. Populations of C. vestalis fell into three groups, pointing to isolation in northwestern and southwestern China and strong genetic differentiation of these populations from others in central and eastern China. In contrast, DBM showed much weaker genetic differentiation and high rates of gene flow. TESS analysis identified the immigrant populations of DBM as showing admixture in northern China. Genetic disconnect between C. vestalis and its host suggests that the parasitoid did not migrate yearly with its host but likely consisted of resident populations in places where its host could not survive in winter.

opencc-zeroDec 2016View details →
zenodo40/100

Figure 3 in Morphogeometric and genetic variations among North African populations of the Mediterranean killifish Aphanius fasciatus (Valenciennes, 1821) from different habitats

Figure 3. – Projection of Procrustes coordinates and scores of canonical variate on Aphanius fasciatus shape analysis (A) and comparative transformation grids (B). LM: Mellah lagoon, M: Mellah marsh, BZ: Lagoon of Bizerte, LA: Ayata Lake.

opencc-by-4.0Dec 2021View details →
zenodo40/100

Figure 2 in Morphogeometric and genetic variations among North African populations of the Mediterranean killifish Aphanius fasciatus (Valenciennes, 1821) from different habitats

Figure 2. – Landmarks distribution on fish body of Aphanius fasciatus. 1: Eye position, 2: Dorsal opercular limit, 3: Beginning of dorsal fin, 4: End of dorsal fin, 5: Dorsal limit of caudal peduncle, 6: Median limit of caudal peduncle, 7: Ventral limit of caudal peduncle, 8: End of anal fin, 9: Beginning of anal fin, 10: Pelvic fin insertion, 11: Ventral opercula limit, 12: Dorsal limit of pectoral fin, 13: Ventral limit of pectoral fin, 14: Mouth.

opencc-by-4.0Dec 2021View details →
zenodo40/100

Figure 1 in Morphogeometric and genetic variations among North African populations of the Mediterranean killifish Aphanius fasciatus (Valenciennes, 1821) from different habitats

Figure 1. – Map of the west Mediterranean basin with North African sample sites. 1: Mellah lagoon (LM), 2: Mellah marsh (M), 3: Lagoon of Bizerte (BZ), 4: Ayata Lake (LA).

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

Population size differences can lead to biases in phylogenetic inference and introgression detection in the presence of purifying selection

<p>Phylogenetic reconstruction and introgression detection rely on an assumption about the probability distribution of gene tree topologies. Recently, evidence has emerged that population size differences can affect the probability distribution of gene tree topologies in the presence of purifying selection. Here, using the population genetic simulator SLiM, we provide evidence that in the presence of purifying selection, population size differences can lead to biases in phylogenetic inference. We also provide evidence that in the presence of purifying selection, population size differences can cause statistics used for introgression detection to exhibit patterns resembling those caused by introgression. In addition, we present a theoretical analysis showing that the occurrence of population size–dependent gene tree distributions is an inherent consequence of purifying selection. Our work underscores the importance of considering the potential confounding effect of purifying selection on phylogenetic inference and introgression detection.</p>

opencc-zeroFeb 2024View details →
zenodo40/100

Fat oxidation rates and cardiorespiratory responses during exercise in different subject populations with post-acute sequelae of SARS-CoV-2 infection: a comparison with normative percentile values

<p>INTRODUCTION:&nbsp;Post-acute sequelae of SARS-CoV-2 infection (PASC) presents a spectrum of symptoms following acute COVID-19, with exercise intolerance being a prevalent manifestation likely linked to disrupted oxygen metabolism and mitochondrial function. This study aims to assess maximal fat oxidation (MFO) and exercise intensity at MFO (FATmax) in distinct PASC subject groups and compare these findings with normative data.</p> <p>METHODS: Eight male subjects with PASC were involved in this study. The participants were divided in two groups: &ldquo;endurance-trained&rdquo; subjects&nbsp;(V̇O<sub>2</sub>max &gt; 55 ml/min/kg) and &ldquo;recreationally-active&rdquo; subjects (V̇O<sub>2</sub>max &lt; 55 ml/min/kg). Each subject performed a graded exercise test until maximal oxygen consumption (V̇O<sub>2</sub>max) to measure fat oxidation. Subsequently, MFO was assessed and FATmax calculated as the ratio between V̇O<sub>2 </sub>at MFO and V̇O<sub>2</sub>max.</p> <p>RESULTS: The MFO and FATmax of &ldquo;endurance-trained&rdquo; subjects were 0.85, 0.89, 0.71 and 0.42, and 68%, 69%, 64% and 53%, respectively. Three out of four subjects showed both MFO and FATmax values placed over the 80<sup>th</sup> percentile of normative data. The MFO and FATmax of &ldquo;recreationally-active&rdquo; subjects were 0.34, 0.27, 0.35 and 0.38, and 47%, 39%, 43% and 41%, respectively. All MFO and FATmax values of those subjects placed below the 20<sup>th</sup> percentile or between the 20<sup>th</sup> and 40<sup>th</sup> percentile.</p> <p>DISCUSSION: Significant differences in MFO and FATmax values between 'endurance-trained' and &ldquo;recreationally-active&rdquo; subjects suggest that specific endurance training, rather than simply an active lifestyle, may provide protective effects against alterations in mitochondrial function during exercise in subjects with PASC.</p>

opencc-by-4.0Dec 2023View details →
dryad40/100

Data from: Genomic landscapes of divergence among island bird populations: evidence of parallel adaptation but at different loci?

<p>When populations colonise new environments they may be exposed to novel selection pressures but also suffer from extensive genetic drift due to founder effects, small population sizes, and limited interpopulation gene flow. Genomic approaches enable us to study how these factors drive divergence, and disentangle neutral effects from differentiation at specific loci due to selection. Here, we investigate patterns of genetic diversity and divergence using whole-genome resequencing (&gt; 22X coverage) in Berthelot's pipit (<em>Anthus berthelotii</em>), a passerine endemic to the islands of three north Atlantic archipelagos. Strong environmental gradients, including in pathogen pressure, across populations in the species range, make it an excellent system in which to explore traits important in adaptation and/or incipient speciation. Firstly, we quantify how genomic divergence accumulates across the speciation continuum, i.e., among Berthelot's pipit populations, between subspecies across archipelagos, and between Berthelot's pipit and its mainland ancestor, the tawny pipit (<em>Anthus campestris</em>). Across these colonisation timeframes (2.1 million – <em>ca.</em> 8,000 years ago), we identify highly differentiated loci within genomic islands of divergence and conclude that the observed distributions align with expectations for non-neutral divergence. Characteristic signatures of selection are identified in loci associated with craniofacial/bone and eye development, metabolism, and immune response between population comparisons. Interestingly, we find limited evidence for repeated divergence of the same loci across the colonisation range but do identify different loci putatively associated with the same biological traits in different populations, likely due to parallel adaptation. Incipient speciation across these island populations, in which founder effects and selective pressures are strong, may therefore be repeatedly associated with morphology, metabolism, and immune defence.</p>

opencc-zeroApr 2024View details →
zenodo40/100

Fig. 6 in Shell Morphology, Growth Pattern And Population Dynamics Of The Land Snail Xerolenta Obvia (Menke, 1828) In Two Areas Of Different Climatic Conditions Within A Temperate Climate Region

Fig. 6. Xerolenta obvia growth model under natural conditions. Size ranges of sexually ma- ture snails are shown in dark grey (4.5–5.4 whorls) and light grey (4.25–4.4 whorls); solid lines = SW population, dashed lines = NE population; 1 = first model variant, 2 = second model variant (details in text)

opencc-by-4.0Mar 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