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8,589 results for “evidence”
U-Pb on zircon data from 'Evidence for large disturbances of the Ediacaran geomagnetic field from West Africa'
<p>This dataset provides the tabular U-Pb data on zircon presented in Robert et al. 2023 'Evidence for large disturbances of the Ediacaran geomagnetic field from West Africa', Precambrian Research, 394, 107095.</p> <p>The data are provided both as an xls formatted as in the original publication (in Table 1), and in a condensed .csv. Please the README file for a description of the columns of the csv.</p>
Data set associated to the manuscript entitled Carbon emissions from inland waters may be underestimated: evidence from European river networks fragmented by drying by López-Rojo et. al
<p>CO2 and CH4 emissions and several associated environmental variables were taken in 6 European drying river networks, in 20 river reaches per river network. The field work was carried across 3 sampling campaigns in 2021, coinciding with 3 hydrological seasons (pre-dry, dry and post-rewetting) to encompass most of the hydrological variability. Each time, measures were taken in the habitats available (flowing water, dry riverbeds, isolated pools).</p>
Data for "Lithium isotope evidence shows Devonian afforestation may have significantly altered the global silicate weathering regime"
<p>This contains measured data for paper "Lithium isotope evidence shows Devonian afforestation may have significantly altered the global silicate weathering regime", under funding of ERC grant 682760 CONTROLPASTCO2. </p> <p>This consists all the Li isotope data obtained from brachiopods/bulk carbonate samples.</p>
Long term effects of payment for performance on maternal and child health outcomes– evidence from Tanzania
<p>These are the datasets underpinning the paper entitled: <strong>Long term effects of payment for performance on maternal and child health outcomes– evidence from Tanzania.</strong></p> <p><strong>The datasets are provided in csv and Stata 16 format along with variable descriptions, and the Stata do file used for analysis.</strong></p>
Periodic Hydraulic Testing Dataset for "Borehole-based fracture unclogging experiment: bridging the gap between laboratory- and field-scale evidence (FRANC)"
<p>This dataset is associated with the SNSF-SPARK project “Borehole-based fracture unclogging experiment: bridging the gap between laboratory- and field-scale evidence (FRANC)”. Please read the ReadMe file for more information.</p>
Data Release: "No evidence that the majority of black holes in binaries have zero spin"
<p>This dataset contains the results presented in "<em>No evidence that the majority of black holes in binaries have zero spin</em>".</p> <p>In this paper, we systematically explored the effective and component spin distributions of binary black holes among the LIGO/Virgo GWTC-3 catalog. In particular, we tried to answer the following core questions, which have been the subject of active exploration and some debate in the literature:</p> <p><em>1. Is there an excess of binary black holes with vanishing spin, as predicted by some theories of angular momentum transport in stellar cores?</em></p> <p><strong>We find no evidence for an excess of vanishing spin systems.</strong> This finding is confirmed by three complementary analyses: one relying only on the Bayes factors between spinning and non-spinning priors for each BBH observation, one that seeks to model the distribution of effective aligned spins, and one modeling the distribution of component spin magnitudes and misalignment angles. Instead, we find BBH spin magnitudes to be consistent with a single, continuous distribution that remains finite at magnitude zero.</p> <p><em>2. Do there exist binaries with component spins misaligned by more than 90 degrees relative to their orbits?</em></p> <p><strong>We find a strong preference for the existence of such strongly misaligned spins.</strong> Our analysis of the BBH component spin distribution indicates that at least some component spins are misaligned from their orbits by more than 90 degrees. This result is robust under a variety of modeling choices regarding both the distribution of component spin magnitudes and tilts.</p> <p>The code used to generate this data can be found in the repository <a href="https://github.com/tcallister/gwtc3-spin-studies/">https://github.com/tcallister/gwtc3-spin-studies/</a>. This repository includes <a href="https://github.com/tcallister/gwtc3-spin-studies/tree/main/data">jupyter notebooks</a> that can be used to open, explore, and plot the files contained in this data set. Additional information about reproducing and/or using this dataset can be found in <a href="https://tcallister.github.io/gwtc3-spin-studies/build/html/index.html">our associated documentation</a>.</p> <p>Further notes:</p> <ul> <li>The files <em>sampleDict_FAR_1_in_1_yr.pickle</em> and <em>injectionDict_FAR_1_in_1.pickle</em>, used as inputs to our analyses, are created via code in the repository <a href="https://github.com/tcallister/get-lvk-data">https://github.com/tcallister/get-lvk-data</a> (see also <a href="https://zenodo.org/record/6505409">https://zenodo.org/record/6505409</a>).</li> <li>The file <em>posteriors_gaussian_spin_samples_FAR_1_in_1.json</em>, used for figure generation, was published by the LIGO Scientific Collaboration, Virgo Collaboration, and KAGRA Collaboration in support of the paper "<a href="https://arxiv.org/abs/2111.03634">The population of merging compact binaries inferred using gravitational waves through GWTC-3</a>" (see <a href="https://zenodo.org/record/5655785">https://zenodo.org/record/5655785</a>).</li> </ul>
Evidence for Early Mesozoic diversification of Hypsimetopidae Nicholls, 1943 (Isopoda), with the description of a new genus from Andhra Pradesh and notes on threats to Indian cave environments
<p>Datafiles and scripts for https://doi.org/10.1093/jcbiol/ruac052</p> <p>Evidence for Early Mesozoic diversification of Hypsimetopidae Nicholls, 1943 (Isopoda), with the description of a new genus from Andhra Pradesh and notes on threats to Indian cave environments</p> <p>George D. F. Wilson1,2 and Shabuddin Shaik 3</p> <p>1 Saugatuck Natural History Laboratory, Saugatuck, MI, USA; gdfw@snhlab.com</p> <p>3 Department of Life Science, Central University of Karnataka, Kadaganchi, 585 367, India; shabu.biologist@gmail.com</p> <p>2 Corresponding author: George D. F. Wilson, P. O. Box 714, Saugatuck, Michigan 49453, USA. e-mail: gdfw@snhlab.com </p> <p>File List:</p> <p>Phreatoi20220525.nex <br> Mesquite data file that contains all data from the DELTA taxonomic database that were used for data presentation, organization, analysis, as well as trees resulting from all analyses. For Mesquite version 3.70; Maddison WP, Maddison DR. 2021. Mesquite: a modular system for evolutionary analysis. Version 3.6 University of British Columbia & Oregon State University., http://www.mesquiteproject.org/ <br> <br> The DELTA database is still being edited and changed so it is not included here<br> For DELTA, see website https://www.delta-intkey.com/<br> publications:<br> Dallwitz MJ. 1980. A general system for coding taxonomic descriptions. TAXON 29: 41-46.<br> Dallwitz MJ, Paine TA, Zurcher EJ. 2000. User's guide to the DELTA system: a general system for processing taxonomic descriptions. CSIRO: Canberra.</p> <p> <br> Phreatoi20220525.tnt - the TNT data file generated by Mesquite<br> Analyses were performed using TNT-64bit, version 1.5, Goloboff PA, Catalano SA. 2016. TNT version 1.5, including a full implementation of phylogenetic morphometrics. Cladistics 32: 221-238.<br> Note: TNT counts zero as a number so the first tree, taxon or k paramter is 0, the second is 1, the third is 2 and so on </p> <p>TNT Scripts were written or modified for this project by George D. F. Wilson. They were run using the console in Ubuntu 20.04 but should work using the console version of TNT in other operating systems available from http://www.lillo.org.ar/phylogeny/tnt/. I recommend using the console because it allows you do to multiple analysis with one script. </p> <p>Each script has a banner that explains what is being done. If this fails to appear the first time, enter n and restart the script</p> <p>These are easily modified in a text editor to change the analysis<br> -- tnt.run : standard run of tnt. <br> -- tnt-jacK.run : symmetric jackknife analysis with concavity parameter, select file, concavity and prob parameter <br> -- piwe_rangeK.run : A range of concavity parameters are selected at the beginning and run sequentially<br> -- setk_trans.run : Modified from setk.run by Salvador Arias, Instituto Miguel Lillo, San Miguel de Tucuman, Argentina<br> -- aquickie_bt1000.run : Modified from the standard script distributed with TNT with more iterations of jackknifing<br> <br> If you are new to using TNT, see the information available on http://www.lillo.org.ar/phylogeny/tnt/ as well as these articles:<br> Goloboff PA. 1993. Estimating character weights during tree search. Cladistics 9: 83-91.<br> Goloboff PA. 1997. Self-Weighted Optimization: Tree Searches and Character State Reconstructions under Implied Transformation Costs. Cladistics 13: 225-245.<br> Goloboff PA, Carpenter JM, Arias JS, Esquivel DRM. 2008. Weighting against homoplasy improves phylogenetic analysis of morphological data sets. Cladistics 24: 758-773.<br> Goloboff PA, Catalano SA. 2016. TNT version 1.5, including a full implementation of phylogenetic morphometrics. Cladistics 32: 221-238.<br> Goloboff PA, Farris JS. 2001. Methods for Quick Consensus Estimation. Cladistics 17: S26-S34.<br> Goloboff PA, Farris JS, Källersjö M, Oxelman B, Ramírez MJ, Szumik CA. 2003. Improvements to resampling measures of group support. Cladistics 19: 324-332.<br> Goloboff PA, Farris JS, Nixon KC. 2008. TNT, a free program for phylogenetic analysis. Cladistics 24: 774-786.</p>
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’ 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’ stress levels through both, a reduced food intake affecting nutritional state and the nestlings’ 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>
Supplementary Materials for "Food security in Roman Palmyra (Syria) in light of paleoclimatological evidence and its historical implications"
<p>Contained here are the SI files for the article "Food security in Roman Palmyra (Syria) in light of paleoclimatological evidence and its historical implications". With all the materials contained here, as well as the openly accessible datasets cited in S1_File, every step of the study can be reproduced. Detailed instructions are contained within. Includes code for Data Analysis.</p> <p>Article DOI: [forthcoming]</p>
Party control, intra-party competition and the substantive focus of women's parliamentary questions: evidence from Belgium (replication data)
<p>Replication data for B. de Vet & R. Devroe, (2022). Party Control, Intraparty Competition, and the Substantive Focus of Women's Parliamentary Questions: Evidence from Belgium. <em>Politics & Gender,</em> 1-25. doi:10.1017/S1743923X21000490</p>
Dataset for "Facsimiles as Epigraphic Evidence: Pitfalls and Opportunities"
<p>This dataset is used in the article "Facsimiles as Epigraphic Evidence: Pitfalls and Opportunities" (Journal of Epigraphic Studies 7, 2024, pp. 9-27). </p> <p>The material was collected through the itemisation of the epigraphic archive collection of Olof August Danielsson (Uppsala University Library). Types of facsimiles, date of creation, creator and references to CIE, Etruskische Texte and CIL were collected during itemisation. Information on type of object and material of object is collected from Etruskische Texte, with additional information from CIE. Method of inscription is collected from CIE. </p>
Supplementary data files for Manzano-Marín 2020 "No evidence for Wolbachia as a nutritional co-obligate endosymbiont in the aphid Pentalonia nigronervosa"
<p>Supplementary data for Manzano-Marín 2019 "No evidence for Wolbachia as a nutritional co-obligate endosymbiont in the aphid Pentalonia nigronervosa".</p> <p>The data in "supplementary_data.tar.gz" consists of six folders:</p> <p>1) "Buchnera_GenBank_annotation”: GenBank-formatted file of the annotated genes of <em>Buchnera</em> from <em>Pentalonia nigronervosa</em> (BPn).</p> <p>2) "Buchnera_gene_BLAST_search”: Tabular BLAST output files and FASTA-formatted files of the identified <em>Buchnera</em> Bpn genes.</p> <p>3) "P_nigronervosa_blastx_binning”: Tabular BLAST output files and FASTA-formatted files of the <em>Buchnera</em>, <em>Wolbachia</em>, and mitochondrion bins.</p> <p>4) "P_nigronervosa_BOWTIE_map_vs_bins": BAM-formatted alignment files for read libraries vs. <em>Buchnera</em> and <em>Wolbachia</em> bins from <em>Pentalonia nigronervosa</em>.</p> <p>5) "P_nigronervosa_BOWTIE_map_vs_genes": BAM-formatted alignment files for read libraries vs. genes from <em>Buchnera</em> and <em>Wolbachia</em> bin from <em>Pentalonia nigronervosa</em>.</p> <p>6) "P_nigronervosa_SPAdes_assembly": Output files for pooled SPAdes assembly.</p> <p>Also, the filtered and trimmed FASTQ files used for genome assembly can be found in the comrpessed file "read_files_clean.tar.gz".</p>
Cross-Domain Modeling of Sentence-Level Evidence for Document Retrieval
<p>This submission includes all pretrained models, test data and prediction files for the EMNLP 2019 paper "Cross-Domain Modeling of Sentence-Level Evidence for Document Retrieval". Please follow the instructions in the emnlp bran at the <a href="https://github.com/castorini/birch/tree/emnlp">Birch repo</a> to reproduce the results.</p>
From Fleece to Thread: Interdisciplinary Evidence for the Origins of Sheep Wool
<p>Supplementary data for the article "From Fleece to Thread: Interdisciplinary Evidence for the Origins of Sheep Wool" by Laura C. Viñas-Caron, Mikkel Nørtoft, Peder Flemestad, Jonas Holm Jæger, Christina Margariti</p> <p>Wool confirmed finds file:</p> <p>Coordinates in X and Y columns in all tables are in the CRS: EPSG 3857<br>Some sites also have WGS 84 lat/long coordinates<br>The majority of the wool finds are from the CINBA project:<br>https://cinba.net/outputs/databases/textiles/<br>with additional finds by Mikkel Nørtoft. </p> <p> </p> <p>Sheep mtDNA file:</p> <p>Spatiotemporal mtDNA metadata on sheep were collected by Laura C. Viñas-Caron.<br>All sites have WGS 84 lat/long coordinates</p>
TABLE 2 in First evidence of cannibalism in Crassimurex (s. s.) calcitrapa (Lamarck, 1803) (Gastropoda, Muricidae) from the Lutetian of the Paris Basin (France)
<p>TABLE 2. — Morphological and functional patterns of holes associated with gastropod and <i>Octopus</i> predation (modified from Gordillo <i>et al.</i> 2022).</p><table><thead><tr><th><b>Characteristic</b></th><th><b>Pattern A</b></th><th><b>Pattern B</b></th><th><b>Pattern C</b></th></tr></thead><tbody><tr><th>Shape</th><td>A hole, round to oval</td><td>Paired breaks</td><td>A hole, rounded to irregular</td></tr><tr><th>Outline character</th><td>Regular outline</td><td>Irregular breakage</td><td>Regular to irregular</td></tr><tr><th>Profile cross section</th><td>Straight or sloping sides or parabolic outline</td><td>Random breakage</td><td>Width and direction of hole vary with depth</td></tr><tr><th>Drill hole location</th><td>Primarily Abapertural, dorsal to ventral</td><td>Unspecified</td><td>Apertural, ventral to dorsal, parietal (left)</td></tr><tr><th>Produced by</th><td>Secretions of the ABO and rasping by the radula</td><td>Possible chemical softening and biting marks of upper and lower beaks</td><td>Secretion of salivary glands and rasping by radula and teeth of the papillary shield and terminal process</td></tr><tr><th>Potential predator</th><td>Drilling gastropods</td><td><i>Octopus</i></td><td><i>Octopus</i></td></tr><tr><th>Present in this sampling</th><td>Yes</td><td>No</td><td>No</td></tr></tbody></table>
CT-EBM-SP - Corpus of Clinical Trials for Evidence-Based-Medicine in Spanish (version 2)
<p>A collection of <strong>1200 texts</strong> (292173 tokens) about<strong> clinical trials studies</strong> and <strong>clinical trials announcements</strong> in <strong>Spanish</strong>:</p> <p>- 500 abstracts from journals published under a Creative Commons license, e.g. available in PubMed or the Scientific Electronic Library Online (SciELO).<br>- 700 clinical trials announcements published in the European Clinical Trials Register and Repositorio Español de Estudios Clínicos.</p> <p>Texts were annotated with the following entities types:</p> <p>- <strong>Semantic groups from the Unified Medical Language System</strong>: <br> • ANAT: anatomy<br> • CHEM: pharmacological and chemical substances<br> • DEVI: medical devices<br> • DISO: pathologic conditions <br> • LIVB: living beings, included the human being<br> • PHYS: physiological processes<br> • PROC: lab tests, diagnostic or therapeutic procedures<br>- <strong>Medical drug information</strong>:<br> • Contraindicated: a contraindicated drug or treatment<br> • Dose: dose or strength<br> • Form: dosage form<br> • Route: administration route or mode<br>- <strong>Temporal expressions</strong> <br> • Age<br> • Date<br> • Duration<br> • Frequency<br> • Time<br>- <strong>Miscellaneous medical entities</strong>: <br> • Concept: abstract concepts, statistical tests or measurement scales<br> • Food: foods or drinks<br> • Observation: medical observations or clinical findings<br> • Quantifier_or_Qualifier: quantifier or qualifier adjective<br> • Result_or_Value: result or value of a measurement, laboratory analysis or procedure<br>- <strong>Negation/Speculation</strong>: <br> • Neg_cue: negation cue<br> • Negated: negated event<br> • Spec_cue: speculation cue<br> • Speculated: speculated or uncertain event<br>- <strong>Attributes</strong>: <br> • Temporality:<br> ◦ History_of: past event<br> ◦ Future: future event<br> • Experiencer:<br> ◦ Patient: patient or participant on a clinical trial<br> ◦ Family_member<br> ◦ Other: other person different from the patient or the family member</p> <p>86 389 entities and 16 590 attributes were annotated. 10% of the corpus was doubly annotated, and high inter-annotator agreement (IAA) values were achieved: F1-score = 0.84% for entities; and F1-score = 0.88% for attributes (both in strict match). </p> <p>The dataset includes the <strong>texts and annotations used for the human evaluation</strong> of the medical named entity tool:</p> <p>- 100 clinical trial announcements from EudraCT not used for system development: we provide files of the version revised by medical professionals (Reference folder)<br>- 100 clinical cases with Creative Commons license: we provide files with the files revised by medical professionals (Reference folder). These data come from:</p> <p> • Urgencias Bidasoa (https://urgenciasbidasoa.wordpress.com/casos-clinicos-3/)<br> • Hipocampo.org (https://www.hipocampo.org/)<br> • Cases published by Sociedad Andaluza de Medicina Familiar y Comunitaria (SAMFyC): we are greatly thankful for giving us permission to use these cases and we acknowledge that the copyright belongs to the authors' contents. Clinical cases were extracted from books published from 2016 to 2022 (https://www.samfyc.es/tipos-publicacion/publicaciones/).<br> <br>If you use these data, please, acknowledge the copyright and intellectual property rights to the authors' contents.</p> <p>The dataset is freely distributed for research and educational purposes under a Creative Commons Non-Commercial Attribution (CC-BY-NC-A) License.</p> <p>If you use the CT-EBM-SP vs. 2 dataset, please, cite as follows:</p> <p>Campillos-Llanos, L., A. Valverde-Mateos & A. Capllonch-Carrion (2024) Hybrid natural language processing tool for semantic annotation of medical texts in Spanish. BMC Bioinformatics. BioMed Central.</p>
Direct molecular evidence for an ancient, conserved developmental toolkit controlling post-transcriptional gene regulation in land plants
<p>In plants, miRNA production is orchestrated by a suite of proteins that control transcription of the pri-miRNA gene, post-transcriptional processing and nuclear export of the mature miRNA. Post-transcriptional processing of miRNAs is controlled by a pair of physically-interacting proteins, HYL1 and DCL1. However, the evolutionary history and structural basis of the HYL1-DCL1 interaction is unknown. Here we use ancestral sequence reconstruction and functional characterization of ancestral HYL1 <em>in vitro</em> and in <em>Arabidopsis thaliana </em>to better understand the origin and evolution of the HYL1-DCL1 interaction and its impact on miRNA production and plant development. We found the ancestral plant HYL1 evolved high affinity for both double-stranded RNA (dsRNA) and its DCL1 partner before the divergence of mosses from seed plants (~500 Ma), and these high-affinity interactions remained largely conserved throughout plant evolutionary history. Structural modeling and molecular binding experiments suggest that the second of two double-stranded RNA-binding motifs (DSRMs) in HYL1 may interact tightly with the first of two C-terminal DCL1 DSRMs to mediate the HYL1-DCL1 physical interaction necessary for efficient miRNA production. Transgenic expression of the nearly 200 Ma-old ancestral flowering-plant HYL1 in <em>A. thaliana</em> was sufficient to rescue many key aspects of plant development disrupted by HYL1<sup>-</sup> knockout and restored near-native miRNA production, suggesting that the functional partnership of HYL1-DCL1 originated very early in and was strongly conserved throughout the evolutionary history of terrestrial plants. Overall, our results are consistent with a model in which miRNA-based gene regulation evolved as part of a conserved plant ‘developmental toolkit’.</p>
Data to support Whitney JL, Coleman RR, Deakos MH "Genomic evidence indicates small island-resident populations and sex-biased behaviors of Hawaiian Reef Manta Rays"
<p>Datasets supporting the manuscript: Whitney JL, Coleman RR, Deakos MH "Genomic evidence indicates small island-resident populations and sex-biased behaviors of Hawaiian Reef Manta Rays". <em>BMC Ecology and Evolution </em><strong>23</strong>, 31 (2023). https://doi.org/10.1186/s12862-023-02130-0</p> <p>Nuclear data:</p> <p>"Mobula-alfredi_nuclear_reference_RAD_contigs.fasta" is a fasta of 359,751 contigs that serve as the reference for nuclear alignment of genotypes to RAD loci. Contigs begin and end with GATC cut site.</p> <p>Mobula-alfredi_nuclear_all_2048snps_38genotypes.vcf is a VCF file with all 2048 nuclear SNPs in final filtered SNP dataset. 38 genotypes are included from Maui Nui and Hawaii Island. This 2048 SNPs includes both 2038 neutral and 10 outlier SNPs. </p> <p>Mobula-alfredi_nuclear_neutral_2038snps_38genotypes.vcf is a VCF file with 2038 neutral nuclear SNPs genotyped in 38 individuals from Maui Nui and Hawaii Island. </p> <p>Mobula-alfredi_nuclear_outliers_10snps_38genotypes.vcf is a VCF file with 10 outlier SNPs genotyped in 38 individuals from Maui Nui and Hawaii Island. </p> <p>Structure (.str) files are also provided in addition to VCFs. In all files Population prefixes M=Maui Nui and K=Hawaii Island. </p> <p>Mitochondrial data:</p> <p>Mobula-alfredi_mitogenome_34haplotypes_9sites_min4x.vcf is a VCF file with 9 variant sites across the mitogenome haplotyped in 34 individuals from Maui Nui and Hawaii Island. </p> <p>Mobula-alfredi_mitogenome_34haplotypes_allsites_min4x.fasta is a FASTA file with whole mitogenomes aligned to OP562409 [https://www.ncbi.nlm.nih.gov/nuccore/OP562409]. Sites with less than 4x coverage were masked with Ns. </p> <p>Mobula-alfredi_mitogenome_reference_OP562409.fasta is a FASTA file containing the <em>Mobula alfredi</em> reference mitogenome OP562409 [https://www.ncbi.nlm.nih.gov/nuccore/OP562409].</p> <p> </p>
Carbon data for: Evidence for the Multiple Benefits of Wetland Conservation in North America
<p>These data were synthesized as part of a rapid evidence assessment of the scientific literature on a wide range of benefits associated with wetland conservation and restoration. Our synthesis emphasized data from North America and especially the United States, although many of the high priority meta-analyses and reviews we incorporated were global in scope. The data in these files represent a range of metrics related to carbon sequestration, storage, or flux compiled from multiple sources for the purposes of summarizing the range of observed values and how they vary across wetland classes or by restoration status. For more detail on the synthesis methods and each set of metrics, please see the full report: </p> <p>Conlisk E, Chamberlin L, Vernon M, Dybala KE. 2022. Evidence for the Multiple Benefits of Wetland Conservation in North America: Carbon, Biodiversity, and Beyond. Point Blue Conservation Science, Petaluma, CA.</p>
Paleomagnetic Evidence of the Deformation of the Pontides during the closure of the Intra-Pontide Ocean in the Early Cretaceous
<p>Several models exist concerning the deformation history of the Pontides in North Anatolia during the Cretaceous period, which vary depending on the positions of the Istanbul and Sakarya zones, the consumption of the northern branches of the Neotethys ocean and the rifting of several sub-basins. Notably, the early Cretaceous tectonic history of the Pontides involved the closure of the northern Neotethys ocean (Intra-Pontide ocean), and the collision between the Istanbul and Sakarya zones, producing thrust structures along the collisional front. The lack of paleomagnetic data providing evidence for this deformation pattern demonstrates that further investigation is required, particularly focusing on the Lower Cretaceous strata in the Pontides. Thus, the present study aimed to examine samples from a total of 78 sites from the Lower-Upper Cretaceous sedimentary rocks, and Middle Eocene to Middle Miocene sedimentary and volcanic rocks. Results of the present study indicated large counter-clockwise rotations up to R±DR=<strong>-</strong>73.9°±9.1°, and small clockwise rotations of R±DR= 14.2°±12.2° in the Istanbul and Sakarya zones, during the Early Cretaceous and Late Cretaceous periods. These rotation patterns are accompanied by the closure of the Intra-Pontide ocean, and the collision between the Istanbul and Sakarya zones during the Early and Late Cretaceous periods. On the other hand, in the Middle Eocene, small counter-clockwise rotations of R±DR=-6.4°±13.9° and R±DR=4.6°±12.9° along the western coastline of the Pontides indicated that the northern margin of the Pontides was stable during this period.</p>
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.