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5,990 results for “reproduction”
Data and Code for "Extracting reproductive parameters from GPS tracking data for a nesting raptor in Europe"
<p>Understanding population dynamics requires estimation of demographic parameters. We build on existing approaches to develop a new tool that uses GPS tracking data to estimate breeding propensity and breeding success, and show that this tool yielded accurate predictions for two red kite populations in Central Europe. The tool is available as an R package at <a href="https://github.com/Vogelwarte/NestTool">https://github.com/Vogelwarte/NestTool</a> and will facilitate the estimation of demographic parameters from tracking data to inform population assessments. The files in this repository contain the data and analytical code to replicate the results of the publication in the Journal of Avian Biology (DOI: 10.1111/jav.03246). The version contained in this repository does not include updates and improvements that occurred after the 29 August 2024.</p>
More social species live longer, have longer generation times, and longer reproductive windows
<p>Data and scripts required to reproduce the results of the manuscript "More social species live longer, have longer generation times, and longer reproductive windows"</p>
Reproduction package for the paper "Two waves of massive stars running away from the young cluster R136"
<h2>Reproduction package for the paper "Two waves of massive stars running away from the young cluster R136".</h2> <ul> <li>This reproduction package aims for open science, with the internal API designation of 'Gold'</li> <li>Authors: M. Stoop, A. de Koter, L. Kaper, S. Brands, S. Portegies Zwart, H. Sana, F. Stoppa, M. Gieles, L. Mahy, T. Shenar, D. Guo, G. Nelemans, S. Rieder</li> <li>Paper DOI: https://doi.org/10.1038/s41586-024-08013-8</li> <li>Zenodo DOI: http://doi.org/10.5281/zenodo.10058762</li> <li>Published in Nature (date of publication: 2024/10/09)</li> </ul> <h2>Hardware</h2> <ul> <li>Tested on a MacBook Pro (13-inch, 2020, Four Thunderbolt 3 ports)</li> <li>Processor: 2 GHz Quad-Core Intel Core i5</li> <li>Memory: 32 GB 3733 MHz LPDDR4X</li> <li>Graphics: Intel Iris Plus Graphics 1536 MB</li> </ul> <h2>Required non-standard hardware</h2> <ul> <li>None</li> </ul> <h2>Software dependencies</h2> <ul> <li>Jupyterlab (4.0.8)</li> <li>Notebook (7.0.6)</li> <li>Programming languages used: Python (3.11.7)</li> <li>Python packages used: numpy (1.25.2), pandas (2.1.4), matplotlib (3.8.0), os (comes with Python) scipy (1.11.4), gaiadr3-zeropoint (0.0.4) https://gitlab.com/icc-ub/public/gaiadr3_zeropoint), astroquery (0.4.6), pymc (5.6.1), corner (2.2.2), arviz (0.16.0), pytensor (2.12.3), lmfit (1.2.2), powerlaw (1.5), rpy2 (3.5.16), seaborn (0.12.2), consistencytest (0.0.2)</li> </ul> <h2>Instructions</h2> <ul> <li>The Anaconda conda environment is given should this be needed</li> <li>All Jupyter Notebooks are ready-made to produce the raw data, intermediate and end data products</li> <li>Gaia raw data is downloaded in the Jupyter Notebook "R136_runaway_candidates.ipynb"</li> <li>Data from the literature is given in the subdirectory /tables/ or /input_files/</li> <li>Input images and files are given in the subdirectory /input_files/</li> <li>Intermediate and end data products are given in /output_files/</li> <li>Figures in the paper are produced in the Jupyter Notebooks in the subdirectory /figures/ and stored in the subdirectory /figures/figures_paper/</li> </ul> <h2>Expected Output</h2> <ul> <li>Jupyter Notebooks can be executed by "Run" -> "Run All Cells"</li> <li>The Jupyter Notebook show the expected output in their respective cell</li> <li>Expected runtime are given at the top of each Jupyter Notebook</li> <li>The Jupyter Notebook which takes the longest "R136_runaway_search.ipynb" takes 7-8 hours for the entire dataset</li> <li>A small dataset has been given in this Jupyter Notebook as a proof-of-concept</li> </ul> <h2>Instructions for use</h2> <ul> <li>Jupyter Notebooks can be executed by "Run" -> "Run All Cells"</li> </ul> <h2>Figures</h2> <ul> <li>Figures can be reproduced from the /figures/ folder.</li> <li>All material and data used are available either in the Raw Data or in the Intermediate Data</li> <li>The figures shown in the paper will be saved in ./figures/figures_paper/ folder.</li> </ul> <pre> </pre>
Reproduction package for: 'Exploring Waveform Variations among Neutron Star Ray-tracing Codes for Complex Emission Geometries'
<p>Data files, python scripts and notebooks to reproduce the code output comparisons performed in "Exploring Waveform Variations among Neutron Star Ray-tracing Codes for Complex Emission Geometries" by Choudhury et al. (2024; <a href="https://doi.org/10.3847/1538-4357/ad7255" target="_blank" rel="noopener"><em>ApJ</em> <strong>975</strong> 202</a>, <a href="https://doi.org/10.48550/arXiv.2406.07285" target="_blank" rel="noopener">arXiv.2406.07285</a>).</p> <p>Please refer to the README for detailed information.</p> <p>N.B. The neutral hydrogen column density (${\rm N}_{\rm H}$) value is mentioned in the paper to be $0.2 \times 10^{20} {\rm cm}^{-2}$, whereas all the analyses in the paper, as reflected in this Zenodo package, actually uses ${\rm N}_{\rm H} = 2 \times 10^{20} {\rm cm}^{-2}$.</p>
Reproduction package for the paper "High-contrast observations of brown dwarf companion HR 2562 B with the vector Apodizing Phase Plate coronagraph"
<p>This is a basic reproduction package for the paper <a href="https://doi.org/10.1093/mnras/stab1893">"High-contrast observations of brown dwarf companion HR 2562 B with the vector Apodizing Phase Plate coronagraph" by Sutlieff et al. (2021)</a>. It aims to provide the most important data products to check and reproduce the main results of the paper.</p>
Reproduction package for the publication 'New radiative loss curve from updates to collisional excitation in the low-density, optically thin plasmas in SPEX'
<p>The following files can be used to reproduce the Figures and data from the paper <strong>New radiative loss curve from updates to collisional excitation in the low-density, optically thin plasmas in SPEX </strong>by L. Štofanová, J. Kaastra, M. Mehdipour, and J. de Plaa accepted to be publish in Section 12. Atomic, molecular, and nuclear data of Astronomy and Astrophysics (acceptance date - 27/06/2021).</p> <p> </p> <p>Note: version 2 is the most updated version (change in Fig.7).</p>
Dataset from: A test of the reproductive assurance hypothesis in Ipomoea hederacea: does inbreeding depression counteract the benefits of self-pollination?
<p><strong>PREMISE: Darwin proposed that self-pollination in allegedly outcrossing species might act as a reproductive assurance mechanism when pollinators or mates are scarce; however, in natural populations, the benefits of selfing may be opposed by seed discounting and inbreeding depression. While empirical studies show variation among species and populations in the magnitude of reproductive assurance, little is known about the counterbalancing effects of inbreeding depression.</strong></p> <p><strong>METHODS: By comparing the female reproductive success of emasculated and open-pollinated flowers, we assessed the reproductive assurance hypothesis in two Mexican populations of <em>Ipomoea hederacea.</em> In one population we assessed temporal variation in reproductive assurance for three years. We evaluated inbreeding depression on seed production, seedling germination, and dry plant mass by contrasting self- and cross-hand pollination treatments in one population for two years.</strong></p> <p><strong> KEY RESULTS: The contribution of self-pollination to female reproductive success was high and consistent between populations, but there was variation in reproductive assurance across years. Inbreeding depression was absent in the early stages of progeny development, but there was a small negative effect of inbreeding in the probability of germination and the mass of adult progeny. </strong></p> <p><strong>CONCLUSIONS: Self-pollination provided significant reproductive assurance in <em>I. hederacea </em>but this contribution was variable across time. The contribution of reproductive assurance is probably reduced by inbreeding depression in later stages of progeny development, but this counter-effect was small in the study populations. This study supports the hypothesis that reproductive assurance with limited inbreeding depression is likely an important selective force in the evolution of self-pollination in the genus <em>Ipomoea</em>. </strong></p>
Warming of experimental plant-pollinator communities advances phenologies, alters traits, reduces interactions, and depresses reproduction
<p>This is the data set supporting the analyses performed in the article entitled "Warming of experimental plant-pollinator communities advances phenologies, alters traits, reduces interactions, and depresses reproduction", by Natasha de Manincor, Alessandro Fisogni, and Nicole E. Rafferty, published in Ecology Letters (2023, 26:323-334, <a href="https://doi.org/10.1111/ele.14158">https://doi.org/10.1111/ele.14158</a>).</p> <p>The experiment has been performed in the greenhouse facilities at the University of California, Riverside, in 2021.</p> <p>The two treatments analyzed are ambient vs warmed (+ 4 °C), the focal pollinator species is <em>Osmia lignaria</em>, and the three focal plant species are <em>Collinsia heterophylla</em>, <em>Nemophila menziesii</em>, and <em>Phacelia campanularia</em>.</p> <p>Data are tab separated .txt files.</p>
Reproduction package for the paper "Measuring the variability of directly imaged exoplanets using vector Apodizing Phase Plates combined with ground-based differential spectrophotometry"
<p>This is a basic reproduction package for the paper <a href="https://doi.org/10.1093/mnras/stad249">"Measuring the variability of directly imaged exoplanets using vector Apodizing Phase Plates combined with ground-based differential spectrophotometry" by Sutlieff et al. (2023)</a>. It aims to provide the most important data products to check and reproduce the main results of the paper.</p>
Data from: Complex climate-mediated effects of urbanization on plant reproductive phenology and frost risk
<p>This dataset comprises crowdsourced data using digitized herbarium specimen images from two comprehensively digitized regional floras; the Consortium of Northeastern Herbaria (CNH; <a href="http://portal.neherbaria.org/portal/">http://portal.neherbaria.org/portal/</a>) and Southeast Regional Network of Expertise and Collections (SERNEC; <a href="http://sernecportal.org/portal/index.php">http://sernecportal.org/portal/index.php</a>) for 200 plant species in the eastern United States, and four reproductive phenophases (i.e., flowering, peak flowering, fruiting, and peak fruiting) extracted from the herbarium specimens with associated climate data from PRISM and human population density from US Census Bureau.</p>
Venkataraman et al. Two novel, tightly linked, and rapidly evolving genes underlie Aedes aegypti mosquito reproductive resilience during drought
<p>VERSION 1: These supplementary files accompany the manuscript by Venkataraman et al. entitled "Rapidly evolving genes underlie Aedes aegypti mosquito reproductive resilience during drought." This includes all raw data in the paper, supplementary data, and instructions for the blood puck feeder.</p> <p>VERSION 2: Supplemental Data Files 16-20 were added on 12/19/2022 to accompany a revision of the original bioRxiv pre-print after peer-review at eLife.</p> <p>VERSION 3: New versions of all files were added on 3/21/2023 to accompany the version of record published in eLife:</p> <p>Krithika Venkataraman , Nadav Shai, Priyanka Lakhiani, Sarah Zylka, Jieqing Zhao, Margaret Herre, Joshua Zeng, Lauren A Neal, Henrik Molina, Li Zhao, Leslie B Vosshall. Two novel, tightly linked, and rapidly evolving genes underlie Aedes aegypti mosquito reproductive resilience during drought. Elife. 2023 Feb 6;12:e80489. PMID: 36744865 DOI: 10.7554/eLife.80489</p>
Asynchronous life cycles contribute to reproductive isolation between two Alpine butterflies
<p>Data from: Asynchronous life cycles contribute to reproductive isolation between two Alpine butterflies</p> <p><strong>Abstract</strong></p> <p>Geographic isolation often leads to the emergence of distinct genetic lineages that are at least partially reproductively isolated. Zones of secondary contact between such lineages are natural experiments that allow investigating how reproductive isolation evolves and co-existence is maintained. While temporal isolation through allochrony has been suggested to promote reproductive isolation in sympatry, its potential for isolation upon secondary contact is far less understood. Sampling two contact zones of a pair of mainly allopatric Alpine butterflies over several years and taking advantage of museum samples, we show that the contact zones have remained geographically stable over several decades. Furthermore, they seem to be maintained by the asynchronous life cycles of the two butterflies, with one reaching adulthood primarily in even and the other primarily in odd years. Genomic inferences document that allochrony is leaky and that gene flow from allopatric sites scales with the degree of geographic isolation. Overall, we show that allochrony has the potential to contribute to the maintenance of secondary contact zones of lineages that diverged in allopatry.</p> <p> </p> <p> </p> <p> </p> <p> </p> <p> </p> <p> </p> <p> </p> <p>Morphology contains the following files:</p> <p>wing_morpho.R<br> R scripts for data transformation of wing shape</p> <p>genital_morpho.R<br> R scripts for data transformation of genital morphology</p> <p><br> Models_used.R:<br> R scripts used to produce the statistical analyses.</p> <p>genital_morpho_master_with_pca.txt<br> Phenotypic data for genital morphology</p> <p>wing_contemporary_morpho_master_with_pca.txt<br> Phenotypic data for contemporary wing patterns</p> <p>wing_historic_morpho_master_with_pca.txt<br> Phenotypic data for wing patterns from museum samples</p> <p>The text files contains the following information:</p> <p>ID = Individual ID<br> genotyped_allopatric = was the individual genotyped<br> latitude<br> longitude<br> DATE = Date of collection<br> DAY = Day of collection<br> MONTH = Month of collection<br> YEAR = Year of collection<br> SPOT = Collection site<br> boxplotID = ID to reproduce boxplot order as used in the paper<br> colory = color code to plot<br> cycle = year cycle (2018/19 or 2020/21)<br> yeartype = even or odd year<br> genital_x_LM1 = linear measure of genital landmark 1 along the x axis<br> genital_y_LM1 = linear measure of genital landmark 1 along the y axis<br> genital_x_LM2 = linear measure of genital landmark 2 along the x axis <br> genital_y_LM2 = linear measure of genital landmark 2 along the y axis <br> genital_x_LM3 = linear measure of genital landmark 3 along the x axis <br> genital_y_LM3 = linear measure of genital landmark 3 along the y axis <br> genital_x_LM4 = linear measure of genital landmark 4 along the x axis <br> genital_y_LM4 = linear measure of genital landmark 4 along the y axis <br> genital_x_LM5 = linear measure of genital landmark 5 along the x axis <br> genital_y_LM5 = linear measure of genital landmark 5 along the y axis <br> v_t1 = length relationship between v and t1<br> v_t2 = length relationship between v and t2 <br> v_t3 = length relationship between v and t3 <br> t3_t1 = length relationship between t3_t1 <br> t3_t2 = length relationship between t3_t2 <br> t2_t1 = length relationship between t2_t1 <br> v_tg = length relationship between v and tg <br> PC1.x = PC1 axis for unprojected morphospace<br> PC2.x = PC2 axis for unprojected morphospace <br> PC3.x = PC3 axis for unprojected morphospace <br> PC4.x = PC4 axis for unprojected morphospace <br> PC5.x = PC5 axis for unprojected morphospace <br> PC6.x = PC6 axis for unprojected morphospace <br> PC7.x = PC7 axis for unprojected morphospace <br> PC1.y = PC1 axis for projected morphospace <br> PC2.y = PC2 axis for projected morphospace <br> PC3.y = PC3 axis for projected morphospace <br> PC4.y = PC4 axis for projected morphospace <br> PC5.y = PC5 axis for projected morphospace <br> PC6.y = PC6 axis for projected morphospace <br> PC7.y = PC7 axis for projected morphospace</p> <p> </p> <p><br> wing_ProcCoord1 = Procrustes coordinate 1<br> wing_ProcCoord2 = Procrustes coordinate 2<br> wing_ProcCoord3 = Procrustes coordinate 3<br> wing_ProcCoord4 = Procrustes coordinate 4<br> wing_ProcCoord5 = Procrustes coordinate 5<br> wing_ProcCoord6 = Procrustes coordinate 6<br> wing_ProcCoord7 = Procrustes coordinate 7<br> wing_ProcCoord8 = Procrustes coordinate 8<br> wing_ProcCoord9 = Procrustes coordinate 9<br> wing_ProcCoord10 = Procrustes coordinate 10<br> wing_ProcCoord11 = Procrustes coordinate 11<br> wing_ProcCoord12 = Procrustes coordinate 12<br> wing_ProcCoord13 = Procrustes coordinate 13<br> wing_ProcCoord14 = Procrustes coordinate 14<br> wing_ProcCoord15 = Procrustes coordinate 15<br> wing_ProcCoord16 = Procrustes coordinate 16<br> wing_ProcCoord17 = Procrustes coordinate 17<br> wing_ProcCoord18 = Procrustes coordinate 18<br> wing_ProcCoord19 = Procrustes coordinate 19<br> wing_ProcCoord20 = Procrustes coordinate 20<br> wing_ProcCoord21 = Procrustes coordinate 21<br> wing_ProcCoord22 = Procrustes coordinate 22<br> wing_ProcCoord23 = Procrustes coordinate 23<br> wing_ProcCoord24 = Procrustes coordinate 24<br> wing_ProcCoord25 = Procrustes coordinate 25<br> wing_ProcCoord26 = Procrustes coordinate 26<br> wing_ProcCoord27 = Procrustes coordinate 27<br> wing_ProcCoord28 = Procrustes coordinate 28<br> wing_ProcCoord29 = Procrustes coordinate 29<br> wing_ProcCoord30 = Procrustes coordinate 30<br> wing_ProcCoord31 = Procrustes coordinate 31<br> wing_ProcCoord32 = Procrustes coordinate 32<br> wing_ProcCoord33 = Procrustes coordinate 33<br> wing_ProcCoord34 = Procrustes coordinate 34<br> wing_ProcCoord35 = Procrustes coordinate 35<br> wing_ProcCoord36 = Procrustes coordinate 36<br> wing_ProcCoord37 = Procrustes coordinate 37<br> wing_ProcCoord38 = Procrustes coordinate 38<br> wing_ProcCoord39 = Procrustes coordinate 39<br> wing_ProcCoord40 = Procrustes coordinate 40<br> wing_ProcCoord41 = Procrustes coordinate 41<br> wing_ProcCoord42 = Procrustes coordinate 42<br> wing_ProcCoord43 = Procrustes coordinate 43<br> wing_ProcCoord44 = Procrustes coordinate 44<br> wing_ProcCoord45 = Procrustes coordinate 45<br> wing_ProcCoord46 = Procrustes coordinate 46<br> wing_ProcCoord47 = Procrustes coordinate 47<br> wing_ProcCoord48 = Procrustes coordinate 48<br> wing_ProcCoord49 = Procrustes coordinate 49<br> wing_ProcCoord50 = Procrustes coordinate 50<br> wing_ProcCoord51 = Procrustes coordinate 51<br> wing_ProcCoord52 = Procrustes coordinate 52<br> wing_ProcCoord53 = Procrustes coordinate 53<br> wing_ProcCoord54 = Procrustes coordinate 54<br> PC1.x = PC1 unprojected<br> PC2.x = PC2 unprojected<br> PC3.x = PC3 unprojected<br> PC4.x = PC4 unprojected<br> PC5.x = PC5 unprojected<br> PC6.x = PC6 unprojected<br> PC7.x = PC7 unprojected<br> PC8.x = PC8 unprojected<br> PC9.x = PC9 unprojected<br> PC10.x = PC10 unprojected<br> PC11.x = PC11 unprojected<br> PC12.x = PC12 unprojected<br> PC13.x = PC13 unprojected<br> PC14.x = PC14 unprojected<br> PC15.x = PC15 unprojected<br> PC16.x = PC16 unprojected<br> PC17.x = PC17 unprojected<br> PC18.x = PC18 unprojected<br> PC19.x = PC19 unprojected<br> PC20.x = PC20 unprojected<br> PC21.x = PC21 unprojected<br> PC22.x = PC22 unprojected<br> PC23.x = PC23 unprojected<br> PC24.x = PC24 unprojected<br> PC25.x = PC25 unprojected<br> PC26.x = PC26 unprojected<br> PC27.x = PC27 unprojected<br> PC28.x = PC28 unprojected<br> PC29.x = PC29 unprojected<br> PC30.x = PC30 unprojected<br> PC31.x = PC31 unprojected<br> PC32.x = PC32 unprojected<br> PC33.x = PC33 unprojected<br> PC34.x = PC34 unprojected<br> PC35.x = PC35 unprojected<br> PC36 = PC36 unprojected<br> PC37 = PC37 unprojected<br> PC38 = PC38 unprojected<br> PC39 = PC39 unprojected<br> PC40 = PC40 unprojected<br> PC41 = PC41 unprojected<br> PC42 = PC42 unprojected<br> PC43 = PC43 unprojected<br> PC44 = PC44 unprojected<br> PC45 = PC45 unprojected<br> PC46 = PC46 unprojected<br> PC47 = PC47 unprojected<br> PC48 = PC48 unprojected<br> PC49 = PC49 unprojected<br> PC50 = PC50 unprojected<br> PC51 = PC51 unprojected<br> PC52 = PC52 unprojected<br> PC53 = PC53 unprojected<br> PC54 = PC54 unprojected<br> PC1.y = PC1 projected<br> PC2.y = PC2 projected<br> PC3.y = PC3 projected<br> PC4.y = PC4 projected<br> PC5.y = PC5 projected<br> PC6.y = PC6 projected<br> PC7.y = PC7 projected<br> PC8.y = PC8 projected<br> PC9.y = PC9 projected<br> PC10.y = PC10 projected<br> PC11.y = PC11 projected<br> PC12.y = PC12 projected<br> PC13.y = PC13 projected<br> PC14.y = PC14 projected<br> PC15.y = PC15 projected<br> PC16.y = PC16 projected<br> PC17.y = PC17 projected<br> PC18.y = PC18 projected<br> PC19.y = PC19 projected<br> PC20.y = PC20 projected<br> PC21.y = PC21 projected<br> PC22.y = PC22 projected<br> PC23.y = PC23 projected<br> PC24.y = PC24 projected<br> PC25.y = PC25 projected<br> PC26.y = PC26 projected<br> PC27.y = PC27 projected<br> PC28.y = PC28 projected<br> PC29.y = PC29 projected<br> PC30.y = PC30 projected<br> PC31.y = PC31 projected<br> PC32.y = PC32 projected<br> PC33.y = PC33 projected<br> PC34.y = PC34 projected<br> PC35.y = PC35 projected</p> <p> </p> <p> </p> <p> </p> <p>Genomics contains the following files (Genomic data is available from NCBI BioProject: PRJNA1019795):</p> <p>all_euryale_calls.vcf.gz<br> The unfiltered VCF file</p> <p>euryale_V2.sh<br> Shell script for the genomic data analysis</p> <p>introgress.R<br> R script for running Introgress</p> <p>introgress_all_east2.txt<br> Output of Introgress for the Eastern contact zone</p> <p>introgress_all_west2.txt<br> Output of Introgress for the Western contact zone</p> <p>Admixture_output.txt<br> Output of Admixture assuming either 2 or 3 genomic clusters (K) with the respective population and ID</p> <p>Outliers2BombyxMori.txt<br> BLAST summary of outlier regions against Bombyx Mori</p> <p>Outliers2ManjolaJurtina.txt<br> BLAST summary of outlier regions against Manjola jurtina</p> <p>Outliers2ParargeAegeria.txt<br> BLAST summary of outlier regions against Pararge aegeria</p> <p> </p>
A battery of in silico models application for pesticides exerting reproductive health effects: assessment of performance and prioritization of mechanistic studies
<p>Dataset of Table 1-7</p> <p>Data of Table 1, “Pesticides and their classification”</p> <p>The Dataset (TIV-D-23-00280R1) contains the original table as PNG-format (TIV-D-23-00280R1_Tab1.PNG). Corresponding raw data is regarding classification in the hazard class reproductive toxicity available on line. All further related information are provided as one meta-data-file (IZSEZO-2L2269_TIV-D-23-00280R1_SK__Tab1_PPP_27_1_M.txt) in txt format.</p> <p> </p> <p>Data of Table 2, “PDB structures of nuclear receptors used in VTL and ED” </p> <p>The Dataset (TIV-D-23-00280R1) contains the original table as PNG-format (TIV-D-23-00280R1_Tab2 15 meta data files as pdf-format with information sources of PDB structures used in employed in silico models (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_2_M1.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_2_M2.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_2_M3.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_2_M4.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_2_M5.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_2_M6.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_2_M7.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_2_M8.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_2_M9.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_2_M10.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_2_M11.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_2_M12.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_2_M13.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_2_M14.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_2_M15.pdf). All further related information are provided as one meta-data-file (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_Tab2_27_2_M.txt) in txt format.</p> <p> </p> <p>Data of Table 3, “Results of in vivo studies (Shepelska et al., 2021; Shepelskaya and Kolyanchuk, 2021; Shepelskaya and Kolianchuk, 2018)”</p> <p>The Dataset (TIV-D-23-00280R1) contains the original table as PNG-format (TIV-D-23-00280R1_Table3.PNG). Three meta data file as pdf-format with data of in vivo studies (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_3_M1.pdf; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_3_M2.pdf; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_27_3_M3.pdf). All further related information are provided as one meta-data-file (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_Tab3_27_3_M.txt) in txt format.</p> <p> </p> <p>Data of Table 4, “Results of in silico modelling of pesticides interaction with nuclear receptors”</p> <p>The Dataset (TIV-D-23-00280R1) contains the original table as PNG-format (TIV-D-23-00280R1 _Tab4.PNG). Corresponding raw data with in silico modelling results provided as two files in CSV format (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_1.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_1-17.csv) and seventeen pdf files (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_1.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_2.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_3.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_4.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_5.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_6.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_7.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_8.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_9.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_10.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_11.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_12.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_13.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_14.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_15.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_16.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_17.pdf). Four meta data file as pdf-format with detailed in silico modelling descriptions (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_1_M1.pdf; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_1_M2.pdf; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_1_M3.pdf; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_M1.pdf). All further related information is provided as one meta-data-file (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_Tab4_24_1-2_M.txt) in txt format.</p> <p> </p> <p>Data of Tabe 5, “Combination of in silico results with in vitro results by considering as positive result only where both in silico models predict a hit (Combined 1)”</p> <p>The Dataset (TIV-D-23-00280R1) contains the original table as PNG-format (TIV-D-23-00280R1 _Tab5.PNG). Corresponding raw data with in silico modelling results provided as two files in CSV format (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_1.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_1-17.csv) and seventeen pdf files (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_1.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_2.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_3.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_4.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_5.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_6.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_7.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_8.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_9.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_10.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_11.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_12.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_13.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_14.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_15.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_16.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_17.pdf). Four meta data file as pdf-format with detailed in silico modelling descriptions (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_1_M1.pdf; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_1_M2.pdf; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_1_M3.pdf; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_M1.pdf).</p> <p>Corresponding raw data with ToxCast results provided as seventeen files in CSV format (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_1.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_2.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_3.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_4.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_5.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_6.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_7.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_8.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_9.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_10.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_11.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_12.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_13.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_14.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_15.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_16.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_17.csv)All further related information is provided as one meta-data-file (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_Tab5_24_25_1_M.txt) in txt format.</p> <p> </p> <p>Data of Table 6, “Combination of in silico results with in vitro results by considering as a positive any in silico hit independently of the employed model (Combined 2)”</p> <p>The Dataset (TIV-D-23-00280R1) contains the original table as PNG-format (TIV-D-23-00280R1 _Tab6.PNG). Corresponding raw data with in silico modelling results provided as two files in CSV format (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_1.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_1-17.csv) and seventeen pdf files (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_1.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_2.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_3.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_4.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_5.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_6.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_7.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_8.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_9.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_10.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_11.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_12.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_13.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_14.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_15.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_16.pdf ; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_17.pdf). Four meta data file as pdf-format with detailed in silico modelling descriptions (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_1_M1.pdf; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_1_M2.pdf; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_1_M3.pdf; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_24_2_M1.pdf).</p> <p>Corresponding raw data with ToxCast results provided as seventeen files in CSV format (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_1.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_2.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_3.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_4.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_5.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_6.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_7.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_8.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_9.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_10.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_11.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_12.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_13.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_14.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_15.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_16.csv; IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_25_1_17.csv)All further related information is provided as one meta-data-file (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_Tab6_24_25_1_M.txt) in txt format.</p> <p> </p> <p>Data of Table 7, “Metrics of performance of in silico models separately and combined.”</p> <p>The Dataset (TIV-D-23-00280R1) contains the original table as PNG-format (TIV-D-23-00280R1 _Tab7.PNG). Corresponding raw data with calculation of relevant performance metrics provided as one file in CSV format (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_26_1.csv). One meta data file as pdf-format with detailed description of the method used for calculation (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_26_1_M1.pdf).</p> <p>All further related information is provided as one meta-data-file (IZSEZO-2L2269_TIV-D-23-00280R1_SK_PPP_Tab7_26_1_M.txt) in txt format.</p>
Reproduction package for the publication 'Prospects for detecting the circum- and intergalactic medium in X-ray absorption using the extended intracluster medium as a backlight'
<p>The uploaded files can be used to reproduce the dataset and figures in the paper<strong> Prospects for detecting the circum- and intergalactic medium in X-ray absorption using the extended intracluster medium as a backlight</strong> by Lýdia Štofanová, Aurora Simionescu, Nastasha A. Wijers, Joop Schaye, Jelle Kaastra, Yannick M. Bahé, and Andrés Arámburo-García.</p><p>NOTE: Files will be published with a new version. </p>
Data and R code for “Individual-level variation in reproductive effort in chestnut oak (Quercus montana Willd.) and black oak (Q. velutina Lam.)”, Forest Ecology and Management, 2022
Masting is a population-level reproductive strategy, where individuals synchronize large but intermittent seed production. Despite the high degree of synchrony at the population level, there can be considerable variation in reproduction among individuals (intraspecific variation). Here, we use 18 years of acorn production data from individual chestnut oak and black oak from control and thinned stands, to understand what factors influence individual differences in reproductive effort and variability. We included a variety of tree-level measurements, environmental characteristics, and measurements from tree cores to determine if certain characteristics were associated variations in reproduction. We considered both mean annual acorn production per m2 crown and interannual variation in acorn production (CV) as response variables. We also classified individuals as super producers (i.e., those that consistently produce more acorns than others), good, fair and poor producers (i.e., those that consistently produce less or have a higher number of failure years). In chestnut oak, 14% of the individuals were classified as super producers and contributed 34% of the total acorns, while poor producers made up 35% of the trees and contributed only 16% to total acorn production. In black oak, super producers (14% of the individuals) contributed 31% of total acorns and poor producers (24% of the individuals) contributed only 9% of the acorns. Diameter at breast height (DBH) was the most consistent variable for explaining intraspecific variation in reproductive effort and variability (i.e., larger individuals had higher mean acorn production for both chestnut oak and black oak, and lower CV for black oak). Other variables that influenced reproduction and variation included elevation and clay content for chestnut oak, and slope for black oak. We found no significant effect from the thinning treatment on acorn production. Our results illustrate how tree-level and environmental characte
California Blue Oak reproduction and recruitment, Sierra Foothills, 2005-2010
This data archive contributes to the study of blue oak conservation by quantifying reproductive success (numbers of new seedlings and their sizes) and survival and growth of the younger life stages (seedlings and saplings), and by exploring how the timing of grazing, topographical variables, and rainfall limit reproduction, growth, and survival for these life stages, helping to identify potential management and restoration strategies to enhance the population viability of blue oak. We followed a population of blue oak (Quercus douglasii) seedlings and saplings in the Sierra Nevada foothills, measuring adult seed production and initial seedling recruitment (number and size of new seedlings), seedling growth and survival, seedling recruitment to saplings (growing greater than 10 cm in height), and sapling growth and survival. We tested the impacts on these demographic processes of timing and intensity of grazing, light availability, water availability, and individual size. We published our analysis of these data as part of the 8th Oak Woodland Symposium. This data archive contains the underlying data for our analysis plus some data we did not include in our analysis (residual dry matter, photosynthetically active radiation, percent exotic/native cover), including raw data and R and Perl scripts used to format them for analysis, and additional information not included in the conference proceedings.
UCSB SONGS Mitigation Monitoring: Wetland Survey - Plant Reproductive Success
These data describe annual estimates of seed set for seven common salt marsh plant species at the San Dieguito Wetland collected as part of the SONGS San Dieguito Wetland Restoration mitigation monitoring program designed to evaluate compliance of the restoration project with conditions of the SONGS permit. Monitoring began in 2012.
Warming and snow experiment plant reproductive and growth data for Saddle, 1993 - 1996.
The International Tundra Experiment (ITEX) is a consortium of research sites seeking to understand the response of tundra plant populations to changes in growing season temperatures through a simple temperature manipulation and transplant experiment. The research goal is to examine the phenologic and reproductive responses of a set of species to experimentally-induced warming at a network of sites. The ITEX design is hierarchical, with sites participating at whatever level they are able. At the minimum, participation in ITEX requires climate monitoring (using the LTER MSR standards), a temperature manipulation using one of three possible designs, and monitoring phenologic and reproductive variables for at least one designated ITEX species or two other species. The temperature manipulation is achieved through use of conical or hexagonal open-top chambers of solar fiberglass, which have been shown to increase the air temperature at the surface approximately 3 degrees C. ITEX studies at Niwot Ridge, a logical outgrowth of the long-term phenology studies there, uses a factorial design based around the long-term snowfence experiment. Twenty cones are placed behind the snowfence, distributed at 10, 25, 45, and 75 m from the fence; each cone is paired with an adjacent plot. Beginning with the 1995 season, 24 additional plots were implemented outside of the snowfence influence. Twelve cones are distributed beyond both the north and south edges of the snowfence area, at 10, 25, 45, and 75 m behind the line of the snowfence; each cone is paired with an adjacent plot. This results in the following treatments: increased winter snow, increased summer temperature, increased snow and increased temperature, and control. Key phenologic, growth, and reproductive traits are being followed on marked individuals of Acomastylis (Geum) rossii and Bistorta (Polygonum) bistortoides, and complete species composition is being monitored.
Fig. 18 in New generic assignment to the harvestman Metaphareus punctatus (Opiliones: Stygnidae) and observations about it reproductive behavior
Fig. 18. Geographical distribution of Eutimesius punctatus (Roewer, 1913), comb. nov. and E. albicinctus (Roewer, 1915).
Fig. 3 in Population and reproductive parameters of the red-tailed catfish, Phractocephalus hemioliopterus (Pimelodidae: Siluriformes), from the Xingu River, Brazil
Fig. 3. Size at first sexual maturity in the red-tailed catfish Phractocephalus hemioliopterus specimens collected from the Xingu River in Pará, Brazil.
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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.
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.