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19,493 results for “Populism”

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dryad40/100

Oenothera Section Calylophus population genetic study

<p><strong>Premise</strong>: Animal pollinators play an important role in pollen dispersal. Differences in foraging patterns, flight distances and grooming behaviors are assumed to have consequences for genetic diversity of plants but are rarely tested explicitly. Here, we assess the role of pollinator functional groups with different foraging behaviors (hawkmoth and bee) in generating patterns of genetic diversity over similar geographic ranges for two closely related taxa.</p> <p><strong>Methods</strong>: This study focuses on two members of <em>Oenothera</em> section <em>Calylophus</em> that co-occur on gypsum outcrops throughout the Chihuahua Desert but differ in floral phenotype and primary pollinator: <em>Oenothera</em> <em>gayleana</em> (bee) and <em>O</em>. <em>hartwegii</em> subsp. <em>filifolia</em> (hawkmoth). We measured breeding system and floral traits in the greenhouse and conducted a population genetic study at the local (&lt;13km; four populations) and landscape (60–440km; five populations) scales using 10–11 nuclear (pollen dispersal) and three plastid (seed dispersal) microsatellite markers. </p> <p><strong>Key Results</strong>: Both taxa were self-incompatible and floral traits were consistent with expectations for different pollinators. We found no evidence of genetic structure at the local scale, but at the landscape scale, <em>O</em>. <em>gayleana</em> showed greater differentiation and significant isolation by distance than <em>O</em>. <em>hartwegii</em> subsp. <em>filifolia</em>. The plastid data were consistent with gravity dispersal of seeds and suggest that pollen dispersal is the principal driver of genetic structure in both species.</p> <p><strong>Conclusions</strong>: We demonstrate that pollinator functional groups can impact genetic differentiation in different and predictable ways. Hawkmoths, with larger foraging distances, can maintain gene flow across greater spatial scales than bees.</p>

opencc-zeroOct 2022View details →
dryad40/100

Multilevel selection on social network traits differs between sexes in experimental populations of forked fungus beetles

<p>Both individual and group behavior can influence individual fitness, but multilevel selection is rarely quantified on social behaviors. Social networks provide a unique opportunity to study multilevel selection on social behaviors, as they describe complex social traits and patterns of interaction at both the individual and group levels. In this study, we used contextual analysis to measure the consequences of both individual network position and group network structure on individual fitness in experimental populations of forked fungus beetles (<em>Bolitotherus</em> <em>cornutus</em>) with two different resource distributions. We found that males with high individual connectivity (strength) and centrality (betweenness) had higher mating success. However, group network structure did not influence their mating success. Conversely, we found that individual network position had no effect on female reproductive success but that females in populations with many social interactions experienced lower reproductive success. The strength of individual-level selection in males and group-level selection in females intensified when resources were clumped together, showing that habitat structure influences multilevel selection. Individual and emergent group social behavior both influence variation in components of individual fitness but impact male mating success and female reproductive success differently, setting up intersexual conflicts over patterns of social interactions at multiple levels. </p>

opencc-zeroOct 2022View details →
dryad40/100

Data from: Local adaptation in shell shape traits of a brooding chiton with strong population genomic differentiation

<p class="MsoNormal"><span>Comparing divergence in quantitative tr</span><span>aits and neutral m</span><span>olecular markers, such as <em>Q</em><sub>ST</sub><em>–F</em><sub>ST</sub> comparisons, provides a means to distinguish between natural selection and genetic drift as causes of population differentiation in complex polygenic traits. </span><em>Onithochiton neglectus</em> (Rochebrune, 1881) is a morphologically variable chiton endemic to New Zealand, with populations distributed over a broad latitudinal environmental gradient. In this species, the morphological variants cluster into two geographically separated shell shape groups, and the phenotypic variation in shell shape has been hypothesised to be adaptive. Here, we assessed this hypothesis by comparing neutral genomic differentiation between populations (<em><span>F<sub>ST</sub></span></em><span>)</span> with an index of phenotypic differentiation (<em>P<sub>ST</sub></em>). We used 7,562 putatively neutral single nucleotide polymorphisms (SNPs) across 15 populations and three clades of <em>O. neglectus</em> throughout New Zealand to infer <em><span>F<sub>ST</sub></span></em>. <em>P<sub>ST</sub></em> was calculated from 18 shell shape traits and gave highly variable estimates across populations, clades and shape groups. By systematically comparing <em>P<sub>ST</sub></em> with <em>F<sub>ST</sub></em><sub>,</sub> we identified evidence of local adaptation in a number of the <em>O. neglectus </em>shell shape traits. This <span>supports the hypothesis that shell shape could be an adaptive trait, potentially correlated with the ability to live and raft in kelp holdfasts.</span></p>

opencc-zeroOct 2022View details →
dryad40/100

Data and R computer code from: Summer elk calf survival in a partially migratory population

<p>These data and computer code (written in R, https://www.r-project.org) were created to statistically evaluate a suite of intrinsic and extrinsic risk factors related to calf elk and their mothers' body condition and age. Specifically, known-fate data were collected from 94 elk calves monitored from 2013-2016 in a partially migratory elk (<em>Cervus</em> <em>canadensis</em>) population in Alberta, Canada. Along with adult female data on pregnancy status, age, and body condition, we created a time-to-event dataset that allowed us to analyze calf mortality risk in a time-to-event approach. We also estimated pooled survivorship and cause-specific mortality, as well as stratifying these metrics by migration tactic (resident vs. eastern migrant). Cox proportional hazards models were used to evaluate calf mortality risk in terms of forage biomass (kg/ha), bear predation risk (from an RSF), and other factors that varied between migration tactics. We tested for differences in a number of maternal reproductive parameters (e.g., pregnancy status) and for calf explanatory variables between migrant and resident elk segments. We also use cumulative incidence functions to estimate cause-specific mortality in this multiple carnivore system. Ultimately, we hope that this work helps wildlife managers anticipate how elk calf survival and partial migration dynamics are affected by grizzly bear predation, and our study builds on a long-term partial migration study at the Ya Ha Tinda Ranch in Alberta, Canada. </p>

opencc-zeroOct 2022View details →
zenodo40/100

Figure 1 in Effect of initial infestation on population fluctuation and spatial distribution of Panonychus citri (Acari: Tetranychidae) on Thomson navel orange in Ghaemshahr, Iran

Figure 1. Population fluctuation of Panonychus citri on Thomson navel orange in a multi-treatment experiment in in 2016. Control treatment = average number of 0.48 mite per leaf; Treatment 1 = average number of 1.12 mites per leaf, Treatment 2 = average number of 1.23 mites per leaf, Treatment 3 = average number of 6.36 mites per leaf, Treatment

opencc-by-4.0Jul 2018View details →
zenodo40/100

Figure 4 in Effect of initial infestation on population fluctuation and spatial distribution of Panonychus citri (Acari: Tetranychidae) on Thomson navel orange in Ghaemshahr, Iran

Figure 4. Population fluctuation of Panonychus citri on Thomson navel orange in a paired-treatment experiment in 2017. Infested treatment = average number of 0.79 mite per leaf, Control treatment = average number of 0.59 mite per leaf.

opencc-by-4.0Jul 2018View details →
zenodo40/100

Figure 2 in Effect of initial infestation on population fluctuation and spatial distribution of Panonychus citri (Acari: Tetranychidae) on Thomson navel orange in Ghaemshahr, Iran

Figure 2. Population fluctuation of Panonychus citri on Thomson navel orange in a multi-treatment experiment in in 2016. Control treatment = average number of 0.2 mite per leaf, Treatment 1 = average number of 0.3 mite per leaf, Treatment

opencc-by-4.0Jul 2018View details →
zenodo40/100

Figure 5 in Effects of climatic parameters on Tetranychus urticae (Acari: Tetranychidae) populations based on remote sensing in the southeastern Caspian Sea

Figure 5. The relationship between UV Aerosol Index extracted from Sentinel-5 imagery and spider mite population (mean score of each window) from June 9, 2020 to September 17, 2020 (First window, May 30 to June 9 was not spider mite distribution data).

opencc-by-4.0Apr 2022View details →
zenodo40/100

Figure 6 in Effects of climatic parameters on Tetranychus urticae (Acari: Tetranychidae) populations based on remote sensing in the southeastern Caspian Sea

Figure 6. The relationship between daily CHIRPS-precipitation and spider mite population (mean score of each window) from June 9, 2020 to September 17, 2020 (First window, May 30 to June 9 was not spider mite distribution data).

opencc-by-4.0Apr 2022View details →
zenodo40/100

Figure 2 in Target-site insensitivity to some acaricides in a field population of Tetranychus urticae Koch (Acari: Tetranychidae) from Egypt

Figure 2. Multiple alignment of the amino acid sequences of T. urticae acetylcholinesterase (AChE) between Eg-Bernasht population and GenBank published populations. Tetranychus urticae AChE sequences were performed local as well as global alignments, using BLASTX search protein databases, using a translated nucleotide (NCBI). Three different specific primer sets (1, 2, and 3; Table 1) contained 422 amino acids of AChE gene. Dots: indicate amino acid similarity. Digital number: amino acid position on the AChE protein.

opencc-by-4.0Apr 2022View details →
zenodo40/100

Figure 1 in Target-site insensitivity to some acaricides in a field population of Tetranychus urticae Koch (Acari: Tetranychidae) from Egypt

Figure 1. Products were imaged on a gel post electrophoresis. Tetranychus urticae acetylcholinesterase (AChE) gene fragment amplified expected sizes (639 bp, 571 bp, and 560 bp), using specific primers sets (1, 2, and 3, respectively). Tetranychus urticae voltage-gated sodium channel (VGSC) gene fragments were amplified products (226 bp, 225 bp, and 292 bp), using specific primers primer sets (4, 5, and 6, respectively). Tetranychus urticae glutamategated chloride channel (GluCl1, GluCl3) genes and chitin synthase 1 (CHS1) gene amplified products (263 bp, 251 bp, 541 bp), using primer sets (7, 8, and 9 respectively). EtBr was added to the gel before electrophoresis to a final concentration of 0.5 μg/ml, followed by separation at 100 V for 1 h. The gel was exposed to UV light and the picture was taken with a gel documentation system. Letter a: sample 1, letter b: sample 2, (-): no DNA templates. M:100 bp DNA ladder.

opencc-by-4.0Apr 2022View details →
zenodo40/100

Figure 9 in Effects of climatic parameters on Tetranychus urticae (Acari: Tetranychidae) populations based on remote sensing in the southeastern Caspian Sea

Figure 9. The relationship between NDVI (10 m) provided form Sentinal-2 and density of spider mite during monitoring windows based on ANOVA for linear regression. The alphabetical letters indicate of the sequence windows from June 9, 2020 to September 17, 2020 (First window, May 30 to June 9 was not spider mite distribution data).

opencc-by-4.0Apr 2022View details →
zenodo40/100

Figure 4 in Effects of climatic parameters on Tetranychus urticae (Acari: Tetranychidae) populations based on remote sensing in the southeastern Caspian Sea

Figure 4. Distribution maps of spider mite based on IDW model during monitoring windows, a–n are the sequence windows form June 9, 2020 to September 17, 2020 (First window, May 30 to June 9 was not spider mite population data).

opencc-by-4.0Apr 2022View details →
zenodo40/100

Figure 8 in Effects of climatic parameters on Tetranychus urticae (Acari: Tetranychidae) populations based on remote sensing in the southeastern Caspian Sea

Figure 8. The relationship between MODIS-Evapotranspiration and spider mite population (mean score of each window) from June 9, 2020 to September 17, 2020. (First window, May 30 to June 9 was not spider mite distribution data).

opencc-by-4.0Apr 2022View details →
zenodo40/100

Figure 3 in Effects of climatic parameters on Tetranychus urticae (Acari: Tetranychidae) populations based on remote sensing in the southeastern Caspian Sea

Figure 3. Spider mite distribution throughout Golestan province; 6 (min.) × 6 (min.) grid cells in the DMS coordinate system (yellow points indicate the monitoring fields).

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

Pest defenses under weak selection exert a limited influence on the evolution of height growth and drought avoidance in marginal pine populations

<p>Whilst droughts, intensified by climate change, have been affecting forests worldwide, pest epidemics are a major source of uncertainty for assessing drought impacts on forest trees. Thus far, little information has documented the adaptability and evolvability of traits related to drought and pests simultaneously. We conducted common-garden experiments to investigate how several phenotypic traits (i.e., height growth, drought avoidance based on water-use efficiency inferred from δ<sup>13</sup>C, and pest resistance based on defense traits) interact in five mature lodgepole pine populations established in four progeny trials in western Canada. The relevance of interpopulation variation in climate sensitivity highlighted that seed-source warm populations had greater adaptive capability than cold populations. In test sites, warming generated taller trees with higher δ<sup>13</sup>C and increased the evolutionary potential of height growth and δ<sup>13</sup>C across populations. We found, however, no pronounced gradient in defenses and their evolutionary potential along populations or test sites. Response to selection was weak in defenses across test sites, but high for height growth, particularly at warm test sites. Response to selection of δ<sup>13</sup>C varied depending on its selective strength relative to height growth. We conclude that warming could promote the adaptability and evolvability of growth response and drought avoidance with limited evolutionary influence from pest (biotic) pressures.</p>

opencc-zeroDec 2021View details →
zenodo40/100

Construction of a SNP fingerprinting database and population genetic analysis of 329 cauliflower cultivars

<p>The VCF file contains the information of 1662 SNP sites of 820 cauliflower inbred lines that were filtered according to a series of stringent conditions.</p>

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

Assessing the value of monitoring to biological inference and expected management performance for a European goose population

<p>1. Informed conservation and management of wildlife require sufficient monitoring to understand population dynamics and to direct conservation actions. Because resources available for monitoring are limited, conservation practitioners must strive to make monitoring as cost-effective as possible.</p> <p>2. Our focus was on assessing the value of monitoring to the adaptive harvest management (AHM) program for pink-footed geese (Anser brachyrhynchus). We conducted a retrospective analysis to assess the costs and benefits of a capture-mark-resight (CMR) program, a productivity survey, and biannual population censuses. Using all available data, we fit an integrated population model (IPM) and assumed that inference derived from it represented the benchmark against which reduced monitoring was to be judged. We then fit IPMs to reduced sets of monitoring data and compared their estimates of demographic parameters and expected management performance against the benchmark IPM.</p> <p>3. Costs and the precision and accuracy of key demographic parameters decreased with the elimination of monitoring data. Eliminating the CMR program, while maintaining other monitoring instruments, resulted in the greatest cost savings, usually with small effects on inferential reliability. Productivity surveys were also expensive and some reduction in survey effort may be warranted. The biannual censuses were inexpensive and generally increased inferential reliability.</p> <p>4. The expected performance of AHM strategies was surprisingly robust to a loss of monitoring data. We attribute this result to explicit consideration of parametric uncertainty in harvest-strategy optimization and the fact that a broad range of population sizes is acceptable to stakeholders.</p> <p>5. Synthesis and applications: Our study suggests that existing or potential monitoring instruments for wildlife populations should be scrutinized as to their cost-effectiveness for improving biological inference and management performance. Using Svalbard pink-footed geese as a case study, we show that the loss of some existing monitoring instruments may not be as adverse as commonly assumed if data are jointly analyzed in an integrated population model. Finally, regardless of the monitoring data available, we suggest that conservation strategies that explicitly account for uncertainty in demography are more likely to be successful than those that do not<span>.</span></p>

opencc-zeroOct 2022View details →
dryad40/100

Data from: Protection status, human disturbance, snow cover and trapping drive density of a declining wolverine population in the Canadian Rocky Mountains

<p>Protected areas are important in species conservation, but high rates of human-caused mortality outside their borders and increasing popularity for recreation can negatively affect wildlife populations. We quantified wolverine (<em>Gulo gulo</em>) population trends from 2011 to 2020 in &gt;14 000 km2 protected and non-protected habitat in southwestern Canada. We conducted wolverine and multi-species surveys using non-invasive DNA and remote camera-based methods. We developed Bayesian integrated models combining spatial capture-recapture data of marked and unmarked individuals with occupancy data. Wolverine density and occupancy declined by 39 percent, with an annual population growth rate of 0.925. Density within protected areas was 3 times higher than outside and declined between 2011 (3.6 wolverines/1000 km2) and 2020 (2.1 wolverines/1000 km2). Wolverine density and detection probability increased with snow cover and decreased near development. Detection probability also decreased with human recreational activity. The annual harvest rate of 13% was above the maximum sustainable rate. We conclude that humans negatively affected the population through direct mortality, sub-lethal effects and habitat impacts. Our study exemplifies the need to monitor population trends for species at risk – within and between protected areas - as steep declines can occur unnoticed if key conservation concerns are not identified and addressed.</p>

opencc-zeroOct 2022View details →
zenodo40/100

High-resolution maps of material stock, population and employment in Austria from 1985 to 2018

<p>Global societal material stocks such as buildings and infrastructure accumulated rapidly within recent decades, along with population growth. Material stocks constitute the physical basis of most socio-economic activities and services, such as mobility, housing, health, or education. The dynamics of stock growth, and its relation to the population that demands those services, is an essential indicator for long-term societal resource use and patterns of emissions. The creation of societal material stock creates path dependencies for future resource use, with an important impact on how the transformation towards sustainable societies can succeed.</p> <p>This dataset features detailed maps of material stock and population, as well as the distribution of jobs, for Austria on a 30m grid. The data is based on recent maps of material stock and building volume (compare to Haberl et al. 2021, doi: 10.1021/acs.est.0c05642, data: https://zenodo.org/record/4522892), recent and historic census data, and a time series of Landsat TM, ETM+, and OLI Earth Observation data.</p> <p><strong>Temporal extent</strong></p> <p>The data contains annual maps from 1985 to 2018.</p> <p><strong>Data format and units</strong></p> <p>Per Austrian federal state, the data come in tiles of 30x30km. The projection is EPSG:3035. The images are compressed GeoTiff files (*.tif). There is a mosaic in GDAL Virtual format (*.vrt), which can readily be opened in most Geographic Information Systems. Please consider the generation of image pyramids before using *.vrt files.</p> <p>All image data has 34 bands, where band 1 is data for 1985, and band 34 is data for 2018.</p> <p>The dataset features</p> <ul> <li>population (Scaled by 100 to reduce data storage size. Divide by 100 to get people per cell)</li> <li>jobs (Scaled by 100 to reduce data storage size. Divide by 100 to get jobs per cell)</li> <li>mass (in tons) of &hellip; <ul> <li>total material stock <ul> <li>material stock in buildings <ul> <li>in commercial and industrial buildings</li> <li>in multi-family residential buildings</li> <li>in high-rise buildings</li> <li>in single-family residential buildings</li> <li>in lightweight buildings</li> </ul> </li> <li>material stock in road infrastructure</li> <li>material stock in rail infrastructure</li> <li>material stock in other infrastructure</li> </ul> </li> </ul> </li> </ul> <p><strong>Further information</strong></p> <p>For further information, please see the publication or contact Franz Schug (fschug@wisc.edu). Visit our <a href="https://boku.ac.at/understanding-the-role-of-material-stock-patterns-for-the-transformation-to-a-sustainable-society-mat-stocks">website </a>to learn more about our project MAT_STOCKS - Understanding the Role of Material Stock Patterns for the Transformation to a Sustainable Society.</p> <p><strong>Funding</strong></p> <p>This research was funded by the European Research Council (ERC) under the European Union&rsquo;s Horizon 2020 research and innovation programme (MAT_STOCKS, grant agreement No 741950).</p> <p>&nbsp;</p>

opencc-by-4.0Oct 2022View details →

ScienceDex guides

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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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

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