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zenodo44/100

Microsatellite genotypes for «Genetic diversity and spatial genetic structure support the specialist‑generalist variation hypothesis in two sympatric woodpecker species»

<p>Species are often arranged along a continuum from &ldquo;specialists&rdquo; to &ldquo;generalists&rdquo;. Specialists typically use fewer resources, occur in more patchily distributed habitats and have overall smaller population sizes than generalists. Accordingly, the specialist-generalist variation hypothesis (SGVH) proposes that populations of habitat specialists have lower genetic diversity and are genetically more differentiated due to reduced gene flow compared to populations of generalists. Here, expectations of the SGVH were tested by examining genetic diversity, spatial genetic structure and contemporary gene flow in two sympatric woodpecker species differing in habitat specialization. Compared to the generalist great spotted woodpecker (<em>Dendrocopos major</em>), lower genetic diversity was found in the specialist middle spotted woodpecker (<em>Dendrocoptes medius</em>). Evidence for recent bottlenecks was revealed in some populations of the middle spotted woodpecker, but in none of the great spotted woodpecker. Substantial spatial genetic structure and a significant correlation between genetic and geographic distances were found in the middle spotted woodpecker, but only weak spatial genetic structure and no significant correlation between genetic and geographic distances in the great spotted woodpecker. Finally, estimated levels of contemporary gene flow did not differ between the two species. Results are consistent with all but one expectations of the SGVH. This study adds to the relatively few investigations addressing the SGVH in terrestrial vertebrates.</p>

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

Summary Statistics from "Meta-GWAS of PCSK9 levels detects two novel loci at APOB and TM6SF2"

<p>GWAMA summary statistics of PCSK9 levels using fixed-effect model. Genome-wide data is given for Europeans with statin adjustment and Europeans without statin treatment only (subset of the population). In addition, locus-wide data of the PCSK9 gene locus for African-Americans without statin treatment is listed.</p> <p>When using this data, please cite: Pott J, Gadin J, Theusch E, et al.. Meta-GWAS of PCSK9 levels detects two novel loci at APOB and TM6SF2. Hum Mol Genet. 2021 Sep 30:ddab279. doi: 10.1093/hmg/ddab279. PMID: 34590679</p> <p>All txt files contain the following columns:</p> <ul> <li>markername</li> <li>chr</li> <li>bp_hg19 (base position according to hg19)</li> <li>ea (effect allele)</li> <li>oa (other allele)</li> <li>eaf (effect allele frequency)</li> <li>info (minimal info score across all used studies)</li> <li>nSamples (sample size per SNP)</li> <li>nStudies (number of studies)</li> <li>beta (effect estimate)</li> <li>se (standard error)</li> <li>p (p-value)</li> <li>I2 (SNP heterogeneity across studies)</li> <li>phenotype (phenotyp setting)</li> </ul>

opencc-by-4.0Nov 2021View details →
zenodo44/100

Complete datasets and code for "Hungry or angry? Experimental evidence for the effects of food availability on two measures of stress in developing wild raptor nestlings"

<p><strong>Abstract</strong></p> <p>Food shortage challenges the development of nestlings; yet, to cope with this stressor, nestlings can induce stress responses to adjust metabolism or behaviour. Food shortage also enhances the antagonism between siblings, but it remains unclear whether the stress response induced by food shortage operates via the individual nutritional state or via the social environment experienced. In addition, the understanding of these processes is hindered by the fact that effects of food availability often co-vary with other environmental factors. We used a food supplementation experiment to test the effect of food availability on two complementary stress measures, feather corticosterone (CORTf) and Heterophil/Lymphocyte-ratio (H/L) in developing red kite (Milvus milvus) nestlings, a species with competitive brood hierarchy. By statistically controlling for the effect of food supplementation on the nestlings&rsquo; body condition, we disentangled the effects of food and ambient temperature on nestlings during development. Experimental food supplementation increased body condition, and both CORTf and H/L were reduced in nestlings of high body condition. Additionally, CORTf decreased with age in non-supplemented nestlings. H/L decreased with age in all nestlings and was lower in supplemented last-hatched nestlings compared to non-supplemented ones. Ambient temperature showed a negative effect on H/L. Our results indicate that food shortage increases the nestlings&rsquo; stress levels through both, a reduced food intake affecting nutritional state and the nestlings&rsquo; social environment. Thus, food availability in conjunction with ambient temperature shape between- and within nest differences in stress load, which may have carry-over effects on behaviour and performance in further life-history stages.</p>

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

Disorder-free localization transition in a two dimensional lattice gauge theory

<p>Data files for Figs 2 and 3 from the paper &quot;Disorder-free localization transition in a two dimensional lattice gauge theory&quot;.</p>

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

Dimethylsulfoniopropionate-derived compound concentrations, volatile organic compound concentrations, and microorganism abundances around two corals and a seaweed in the reefs of Moorea (French Polynesia)

<p>These data belong in the paper:&nbsp;</p> <p>M. Masdeu-Navarro, J-F. Mangot, L. Xue, M. Cabrera-Brufau, S.G. Gardner, D.J. Kieber, J.M. Gonz&aacute;lez, R. Sim&oacute; (2022). Spatial and diel patterns of volatile organic compounds, DMSP-derived compopunds and planktonic microorganisms around a tropical scleractinian coral colony. <em>Frontiers in Marine Science</em>.</p> <p>Concentrations of DMSP, acrylate, DMSO, DMS, DMDS, COS, CS2, isoprene, CH3I, CH2ClI, CH2Br2 and CHBr3 in seawater samples around colonies of the corals Acropora pulchra and Pocillopora sp., and the brown seaweed Turbinaria ornata. Abundances of high-DNA and low-DNA bacteria, Prochlorococcus, Synechococcus, picoeukaryotes and nanoeukaryotes in the same samples, as determined by flow cytometry. All samples were collected in April 2018 in the coral reefs of Mo&#39;orea, French Polynesia.&nbsp;</p> <p>The upper set of data&nbsp;contains concentrations at the distance of 0.5 cm from the coral polyps on the branch tips or verrucae, as well as from the seaweed thalli (samples IN), and 2 m away, downcurrent (samples OUT). The second set of data corresponds to A. pulchra only, and contains seawater samples IN, OUT and AL, the latter being sampled&nbsp;at 0.5 cm&nbsp;from the base of the dead branches colonized by a turf alga. IN, OUT and AL samples were collected over an entire diel cycle, every 6 hours for a period of 30 hours.</p>

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

Intraspecific variation in reproductive barriers between two closely-related Arabidopsis sister species

<p>Reproductive isolation (RI) is a critical component of speciation and varies strongly in timing and strength among different sister taxa, depending e.g.<em>,</em> on the geography of speciation and divergence time. However, these factors may also produce variation in timing and strength among populations within species. Here we tested for variation in the expression of RI among replicate population pairs between the sister taxa <em>Arabidopsis lyrata</em> subsp. <em>lyrata</em> and <em>A. arenicola</em>. While the former is predominantly outcrossing, the latter is predominantly selfing<em>.</em> We focused on intrinsic prezygotic and postzygotic RI as both species occur largely in allopatry. We assessed RI by performing within-population crosses and interspecific between-population crosses, and by raising offspring. RI was generally high between all interspecific population pairs, but it varied in timing and strength depending on population history. Prezygotic isolation was strongest between the closest-related population pair, while early postzygotic isolation was high for all other population pairs. Furthermore, the timing and strength of RI depended strongly on cross direction. Our study provides empirical support that reproductive barriers between species are highly variable among population pairs and asymmetric within population pairs, and this variation seems to follow patterns typically described across species pairs.</p>

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

Data for the "Technical Note: assessing predicted cirrus ice properties between two deterministic ice formation parameterizations" manuscript

<p>This repository contains the post-processed ECHAM-HAM data files for comparing KM21_GCM and ML20 of &quot;Technical Note: assessing predicted cirrus ice properties between two deterministic ice formation parameterizations&quot; study.</p> <p>The files are all netCDF4.</p>

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

Simulated microwave brightness temperatures based on two radiosoundings performed during the MOSAiC expedition

<p>This data set contains simulated brightness temperatures in the microwave spectrum for a summer case and a winter case based on radiosoundings performed during the Multidisciplinary drifting Observatory for the Study of Arctic Climate (MOSAiC) expedition&nbsp;<strong>[1]</strong>. The simulations cover the frequencies 1-400 GHz and have been performed with the Passive and Active Microwave radiative TRAnsfer model (PAMTRA, <strong>[2]</strong>). Dimensions 'grid_x', 'grid_y', 'outlevel' can be truncated as they have the length 1. To get simulated brightness tempeartures (TBs) of a zenith-looking microwave radiometer, chose the last index of the dimension 'angles' (which is zenith angle 0&deg;) and average over the 'passive_polarization' dimension. The data has been used to generate Fig. 1 of&nbsp;<strong>[3]</strong>.</p> <p>&nbsp;</p> <p><strong>[1]:</strong> Maturilli, M., Holdridge, D. J., Dahlke, S., Graeser, J., Sommerfeld, A., Jaiser, R., Deckelmann, H., Schulz, A.: Initial radiosonde data from 2019-10 to 2020-09 during project MOSAiC [dataset publication series]. Alfred Wegener Institute, Helmholtz Centre for Polar and Marine Research, Bremerhaven, PANGAEA, https://doi.org/10.1594/PANGAEA.928656, 2021.</p> <p><strong>[2]:</strong> Mech, M., Maahn, M., Kneifel, S., Ori, D., Orlandi, E., Kollias, P., Schemann, V., and Crewell, S.: PAMTRA 1.0: the Passive and Active Microwave radiative TRAnsfer tool for simulating radiometer and radar measurements of the cloudy atmosphere, Geoscientific Model Development, 13, 4229&ndash;4251, https://doi.org/10.5194/gmd-13-4229-2020, 2020.</p> <p><strong>[3]:</strong> Walbr&ouml;l, A., Griesche, H. J., Mech, M., Crewell, S., and Ebell, K.: Combining low- and high-frequency microwave radiometer measurements from the MOSAiC expedition for enhanced water vapour products, Atmospheric Measurement Techniques, 17, 6223-6245, https://doi.org/10.5194/amt-17-6223-2024, 2024.</p>

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

Data supporting 3D Super-resolution Optical Fluctuation Imaging with Temporal Focusing with two-photon excitation

<p>Data to support the publication combining temporal focusing two photon excitation with super-resolution optical fluctuation imaging.</p> <div>This research was funded by National Centre of Science, grant number: 2022/47/B/ST7/03465. For the purpose of Open Access, the author has applied a</div> <div>CC-BY public copyright licence to any author Accepted Manuscript (AAM) version arising from this submission</div>

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

Data set: Variations in water economy traits in two Sphagnum species across their distribution boundaries

<p><em>Sphagnum</em> trait data collected (2016-2017) across a climatic gradient in Sweden. Trait data for both shoot and canopy traits. Data for <em>Sphagnum cuspidatum</em> and <em>Sphagnum lindbergii</em>. Also contains data on species occurrence records in Sweden and output from speceis distribution modelling. See published paper for more information.</p> <p>Files contain (i) processed data ("calculated_trait_data...cvs"), (ii) raw data ("Campbell_etal_clim_traits_...cvs"), (iii) their readme files, and (iv) R-scripts to run the analyses. Note that you need the files in the zip-file to run the analyses in the R-script. The zip-file contains all raw data (climate, traits, species occurences), MaxEnt output, and raster files from photogrammetry.</p> <p>More info in paper: <a href="https://doi.org/10.1002/ajb2.16347" target="_blank" rel="noopener">https://doi.org/10.1002/ajb2.16347</a></p>

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

Molecular simulations of nanoscale two-phase Couette flow of a water-hexane system on a hydrophobic substrate

<p>This dataset contains the output of Molecular Dynamics simulations (MD) of two-phase Couette flow of water/hexane biphasic systems, in terms of density, velocity and temperature fields. Instructions on how to read and analyze the output files in the <code>.tar.gz</code> archives can be found in these previously-published datasets:&nbsp;<a href="https://doi.org/10.5281/zenodo.8077915">https://doi.org/10.5281/zenodo.8077915</a>, <a href="https://doi.org/10.5281/zenodo.6541983">https://doi.org/10.5281/zenodo.6541983</a></p> <p>The run output files are labeled using the following pattern: <code>hex-ca&lt;capillary-number&gt;-q&lt;partial-charge&gt;.tar.gz</code>. It is possible to obtain the wall speed/contact line speed from the capillary number using the following formula:&nbsp;<code>u_w = U_0*&lt;capillary-number&gt;</code>,&nbsp;with <code>U_0 = 37.246 m/s</code>.</p> <p>To reproduce the runs it is necessary to use a specific version of Gromacs that allows for a special algorithm of pressure scaling with position restraints. The code can be obtained by cloning&nbsp;<a href="https://github.com/MicPellegrino/gromacs-flow-field.git">https://github.com/MicPellegrino/gromacs-flow-field.git</a>, and switching to the <code>flow-field-grid-visco-coms-deform</code> branch.</p> <p>The folder&nbsp;<code>conf-wat-hex.zip</code> contains the configuration files to reproduce MD simulations. To prepare the equilibration runs at constant pressure, run after having installed Gromacs:</p> <p><code>gmx grompp -f npt.mdp -p topology.top -c before-npt.gro -r before-npt.gro -o system-npt.tpr</code></p> <p>while to prepare the shear runs:</p> <p><code>gmx grompp -f shear.mdp -p topology.top -c after-npt.gro -r lambda0.gro -rb lambda1.gro -o system-shear.tpr</code></p> <p>Simulations are launched by running:</p> <p><code>gmx mdrun -v -s &lt;tpr-file-name&gt;.tpr &lt;possibly-other-mdrun-flags&gt;</code></p> <p>Have fun simulating!</p>

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

Molecular simulations of nanoscale two-phase Couette flow of a water-hexane system on a hydrophilic substrate

<p>This dataset contains the output of Molecular Dynamics simulations (MD) of two-phase Couette flow of water/hexane biphasic systems, in terms of density, velocity and temperature fields. Instructions on how to read and analyze the output files in the <code>.tar.gz</code> archives can be found in these previously-published datasets:&nbsp;<a href="https://doi.org/10.5281/zenodo.8077915">https://doi.org/10.5281/zenodo.8077915</a>, <a href="https://doi.org/10.5281/zenodo.6541983">https://doi.org/10.5281/zenodo.6541983</a></p> <p>The run output files are labeled using the following pattern: <code>hex-ca&lt;capillary-number&gt;-q&lt;partial-charge&gt;.tar.gz</code>. It is possible to obtain the wall speed/contact line speed from the capillary number using the following formula:&nbsp;<code>u_w = U_0*&lt;capillary-number&gt;</code>,&nbsp;with <code>U_0 = 37.246 m/s</code>.</p> <p>To reproduce the runs it is necessary to use a specific version of Gromacs that allows for a special algorithm of pressure scaling with position restraints. The code can be obtained by cloning&nbsp;<a href="https://github.com/MicPellegrino/gromacs-flow-field.git">https://github.com/MicPellegrino/gromacs-flow-field.git</a>, and switching to the <code>flow-field-grid-visco-coms-deform</code> branch.</p> <p>The folder&nbsp;<code>conf-wat-hex.zip</code> contains the configuration files to reproduce MD simulations. To prepare the equilibration runs at constant pressure, run after having installed Gromacs:</p> <p><code>gmx grompp -f npt.mdp -p topology.top -c before-npt.gro -r before-npt.gro -o system-npt.tpr</code></p> <p>while to prepare the shear runs:</p> <p><code>gmx grompp -f shear.mdp -p topology.top -c after-npt.gro -r lambda0.gro -rb lambda1.gro -o system-shear.tpr</code></p> <p>Simulations are launched by running:</p> <p><code>gmx mdrun -v -s &lt;tpr-file-name&gt;.tpr &lt;possibly-other-mdrun-flags&gt;</code></p> <p>Have fun simulating!</p>

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

Dataset for the comparison of performance of two leak detectors using hydrogen reference leaks (supplement to paper "Advancing Hydrogen Leak Detection: Design and Calibration of Reference Leaks")

<p>Excel file containing some measurements made in December 2023, using three hydrogen reference leaks, to assess the performance of two distinct leak detectors, one portable and made specifically for hydrogen and one MSLD in hydrogen-mode.</p>

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

Methodological and practical lessons learned from exploring the material criticality of two hydrogen-related products

<p>As the European Union embarks on the energy transition, several challenges need to be faced to ensure that this shift is conducted from a holistic perspective that avoids burden-shifting across sustainability dimensions. One of&nbsp;the main concerns refers to the future availability of materials that clean technologies require. Critical raw<br>material assessment serves to guide the management of such mineral resources in a new paradigm of increasing&nbsp;demand. This work delves into the methodological fundamentals of several product-level criticality indicators in&nbsp;order to discuss their implications within the context of the ecodesign of two hydrogen-related products. Overall,&nbsp;criticality is advised to be assessed making use of several indicators. In the case study of a proton exchange&nbsp;membrane fuel cell stack, the combined interpretation of criticality indicators leads to identifying platinum as&nbsp;the main hotspot, while yttrium and lanthanum account for the most relevant criticality contributions in the case<br>study of a solid oxide electrolysis cell stack.</p>

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

Data and analysis code for a toxin induction study on two species of Dinophysis dinoflagellates

<h3>General description</h3> <p>This repository contains the datasets, analysis code and output generated and used in the manuscript "Effects of copepod chemical cues on intra- and extracellular toxins in two species of <em>Dinophysis</em>", which has been published as a research article in Harmful Algae (https://doi.org/10.1016/j.hal.2024.102793).</p> <h3>Files</h3> <p><strong>HRMS_data_Dinophysis_induction_experiment.zip&nbsp;</strong>contains the source high-resolution mass-spectroscopy endometabolomics data in open file formats.</p> <p><strong>Put_annot_sign_affect_feat_metabol_data.xlsx</strong> (corresponds to&nbsp;<strong>Supplementary spreadsheet 1</strong> in the main manuscript) contains putative annotations of significantly affected features from the metabolomics data, for each <em>Dinophysis&nbsp;</em>species (<em>D.</em> <em>sacculus&nbsp;</em>and <em>D. acuminata</em>) and each mode of ionization. Notably, results obtained from GNPS (Global Natural Products Social Molecular Networking,&nbsp;<a href="https://gnps.ucsd.edu/" target="_blank" rel="noopener noreferrer">https://gnps.ucsd.edu/</a>), and SIRIUS (<a href="https://bio.informatik.uni-jena.de/sirius/" target="_blank" rel="noopener noreferrer">https://bio.informatik.uni-jena.de/sirius/</a>) were mentionned. When available, MS/MS spectra were also provided.&nbsp;</p> <p><strong>Tabl_sign_affect_feat.xlsx</strong> (corresponds to&nbsp;<strong>Supplementary spreadsheet 3</strong> in the main manuscript) contains tables of significantly affected features (ANOVA, Tukey&rsquo;s post hoc test, adjusted p-value cut-offs of 0.001 or 0.01) from the metabolomics data, for each <em>Dinophysis&nbsp;</em>species (<em>sacculus&nbsp;</em>and&nbsp;<em>acuminata</em>) and each mode of ionization.&nbsp;A visual representation (heatmaps) of these significant fetures are available as Figs S3-S6 in the supplementary information of the main mauscript.&nbsp;</p> <p><strong>Toxin_analysis_code_output.Rmd</strong>&nbsp;is the R-markdown file that produces the interactive analysis output output (<strong>Toxin_analysis_code_output.html</strong>, corresponds to&nbsp;<strong>Supplementary code &amp; output&nbsp;</strong>in the main manuscript) of the toxin analysis, and uses the datasets <strong>Toxin_analysis_data.csv</strong>,<strong>&nbsp;&nbsp;pca_score_sacculus.csv</strong>,<strong>&nbsp;</strong>and<strong>&nbsp;pca_score_acuminata.csv</strong>&nbsp;source datasets to perform the statistical analyses and generate figures (details for each dataset below).</p> <p><strong>Toxin_analysis_data.csv</strong> (corresponds to&nbsp;<strong>Supplementary spreadsheet 2</strong>&nbsp;in the main manuscript) contains the main data used to statistically analyse the toxin and growth dynamics of both&nbsp;<em>Dinophysis</em> species in response to different grazer treatments, and to produce the majority of the figures in the main manuscript (Figs. 2-6) and supplementary information (Figs. S1-S2).&nbsp;</p> <p><strong>pca_score_sacculus.csv</strong> &amp; <strong>pca_score_acuminata.csv</strong> contain the scores of the first two principal components of the PCA performed on LC-HRMS derived metabolomic profiles of&nbsp;<em>D. sacculus </em>and <em>D. acuminata</em> respectively, in both positive and negative ion mode. These are used to produce PCA score plots (Fig. 6 in the main manuscript and Fig. S2 in the supplementary information).</p> <p><strong>custom.css</strong> is a custom html style sheet file that formats the <strong>Toxin_analysis_code_output.html</strong> to display scrollable tables correctly. It is used by <strong>Toxin_analysis_code_output.Rmd </strong>and is necessary for true reproduction of the output (<strong>.html</strong>) file.</p>

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

Two-time correlation function based on speckle patterns from x-ray photon correlation spectroscopy associated with "Intermittent cluster dynamics and temporal fractional diffusion in a bulk metallic glass" (scientific article published in Nature Communications, 2024)

<p>This dataset consists of contrast data, i.e., the two-time correlation function, based on speckle patterns measured at the at the 8ID-E beamline of the Advanced Photon Source at Argonne National Laboratory.</p> <p>Experimental details are stated in the paper specified under "related work" and in the accompanying supplementary information.</p> <p>You are welcome to use this dataset in compliance with the CC BY 4.0 licence assigned to this dataset.</p> <p>Any questions regarding the data can be addressed to birte.riechers@bam.de who would also appreciate a note if you find the data useful.</p> <p>____________________________________________________________________</p> <p>The data consists of 32 text files in total, which correspond to the main and lower panel Figure 2 of the main publication.&nbsp;</p> <p>30 of these text files are contrast data, which are named "contrast_DT250s_nn.text" wiith "nn" as the identifier of consecutive data sets going from 1 to 30. Each data set consists of p rows and q columns, DT250s denotes the time resolution of data points, which is 250 s along both row and column values.</p> <p>The data set called "Time_Contrast_1to30s.txt" states the start time in seconds of the first data point of each of the thirty contrast data set.</p> <p>The data set called "ScatteredIntensity.txt" states the scattered intensity at full time resolution, i.e. 2.5 s.</p> <p>The files are plain text files with the data points separated by "space" along rows and "new line" along columns.</p>

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

Tailoring PVDF Membranes Surface Topography and Hydrophobicity by a Sustainable Two-Steps Phase Separation Process: dataset

<p>This is the dataset related to the article published in ACS Sustainable Chemistry &amp; Engineering &ldquo;Tailoring PVDF Membranes Surface Topography and Hydrophobicity by a Sustainable Two-Steps Phase Separation Process&rdquo; DOI: 10.1021/acssuschemeng.8b01407</p>

opencc-by-4.0Jun 2018View details →
zenodo44/100

Simulated climate change reduced the capacity of lichen-dominated biocrusts to act as carbon sinks in two semi-arid Mediterranean ecosystems

<p>&nbsp;Biocrust gas exchange measurements used as input data for this study. The methods are described in detail in the related identifier paper.</p>

opencc-by-4.0Aug 2018View details →
zenodo44/100

Data and materials for Wallace et al (2018) Self-report versus electronic medical record recorded healthcare utilisation in older community-dwelling adults: comparison of two prospective cohort studies v1.2

<p>This comprises the data and materials for the study:&nbsp;Wallace&nbsp;E, Moriarty&nbsp;F, McGarrigle&nbsp;C, Smith&nbsp;SM, Kenny&nbsp;RA, Fahey T. (2018)&nbsp;Self-report versus electronic medical record recorded healthcare utilisation in older community-dwelling adults: Comparison of two prospective cohort studies. PLOS ONE 13(10): e0206201.&nbsp;<a href="https://doi.org/10.1371/journal.pone.0206201">https://doi.org/10.1371/journal.pone.0206201</a></p> <p>The anonymised TILDA&nbsp;dataset is publicly available to researchers who meet the criteria for access, at no monetary cost, from the Irish Social Science&nbsp;Data&nbsp;Archive (ISSDA) at University College Dublin (<a href="https://emea01.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.ucd.ie%2Fissda%2Fdata%2Ftilda%2F&amp;data=02%7C01%7C%7Ccc2345c4f5c543bbcddc08d5fd28200c%7C607041e7a8124670bd3030f9db210f06%7C0%7C0%7C636693271128219875&amp;sdata=%2Fcochi1RuRtYSUa5sF9uA%2BjOOoNYIg7DPpk0mZl5D2s%3D&amp;reserved=0">http://www.ucd.ie/issda/data/tilda/</a>) and the Interuniversity Consortium for Political and Social Research (ICPSR) at the University of Michigan (<a href="https://emea01.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.icpsr.umich.edu%2Ficpsrweb%2FICPSR%2Fstudies%2F34315&amp;data=02%7C01%7C%7Ccc2345c4f5c543bbcddc08d5fd28200c%7C607041e7a8124670bd3030f9db210f06%7C0%7C0%7C636693271128219875&amp;sdata=7LHSSqU8xotACMsalpAjVrV5m95DlapgQViyr4P%2FsXY%3D&amp;reserved=0">http://www.icpsr.umich.edu/icpsrweb/ICPSR/studies/34315</a>). For the CPCR cohort, no provision for&nbsp;data&nbsp;sharing was included in the original ethical approval and participant consent form. As a minimal&nbsp;data&nbsp;set necessary to replicate the present study could not be deidentified due to the large number of demographic variables considered, a synthetic version of the study&nbsp;dataset was produced using the synthpop package in R:&nbsp;<a href="https://emea01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fcran.r-project.org%2Fweb%2Fpackages%2Fsynthpop%2Findex.html&amp;data=02%7C01%7C%7Ccc2345c4f5c543bbcddc08d5fd28200c%7C607041e7a8124670bd3030f9db210f06%7C0%7C0%7C636693271128229884&amp;sdata=j3If%2FNe%2F1eGsGAt9hyg3ICMqmLec4aOrjRVKppaRSFU%3D&amp;reserved=0">https://cran.r-project.org/web/packages/synthpop/index.html</a>. This&nbsp;dataset and the analytical code for the present study are presented here. Code&nbsp;developed on the synthetic data&nbsp;can be sent to frankmoriarty@rcsi.ie or&nbsp;<a href="mailto:enquiries.cpcr@rcsi.ie">enquiries.cpcr@rcsi.ie</a>&nbsp;to be run on the original&nbsp;data.</p> <p>v1.2 includes a more detailed description of how the dataset was synthesised.</p>

opencc-by-4.0Aug 2018View details →
zenodo44/100

Compression tests and direct shear test of two types of railway ballast

<p>This data set contains measurement data from uniaxial compression tests and direct shear tests<br> &nbsp;conducted on two types of railway ballast.<br> For a detailed description of the experiments see:</p> <p>B. Suhr, S. Marschnig and K. Six:<br> &quot;Comparison of two different types of railway ballast in compression and direct shear tests:<br> experimental results and DEM model validation&quot;<br> Granular Matter (2018)<br> Doi: 10.1007/s10035-018-0843-9</p> <p>For the uniaxial compression tests, measured normal forces and vertical paths are provided.<br> The direct shear tests are conducted directly afterwards, i.e. the information for<br> one compression and one shear test are contained in only one file.<br> For the shear tests shear paths, shear forces and vertical path are provided.</p> <p>At first the uniaxial compression test is carried out. At the end of this test, the normal load is equal to zero.<br> For the following direct shear test, the normal load is constant (according to the load specified in the file name)<br> and not recorded in the file.<br> The direct shear test starts, when the measured shear path is greater than zero.</p> <p>Check the README.txt file for more information.&nbsp;</p>

opencc-by-4.0Sep 2018View details →

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