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Figure S1. Mediation analysis on the effect of insulin resistance on intraocular pressure. Figure S2. Forest plot showing the OR (95% CI) for EIOP of ALD versus NAFLD and the OR (95% CI) for EIOP of drinkers versus non-drinkers. Abbreviations: OR, odds ratio; CI, confidence interval; ALD, alcoholic liver disease; NAFLD, non-alcoholic fatty liver disease.
<p>Figure S1. Mediation analysis on the effect of insulin resistance on intraocular pressure.</p> <p>Figure S2. Forest plot showing the OR (95% CI) for EIOP of ALD versus NAFLD and the OR (95% CI) for EIOP of drinkers versus non-drinkers. Abbreviations: OR, odds ratio; CI, confidence interval; ALD, alcoholic liver disease; NAFLD, non-alcoholic fatty liver disease.</p>
Temporal evolution of plutonium concentrations and isotopic ratios, cesium activity concentrations, granulometric parameters and organic matter properties in the Ukedo–Takase Rivers draining the Difficult-To-Return Zone in Fukushima, Japan (2013–2020)
<p>The current dataset was compiled to investigate the temporal evolution of plutonium concentrations, isotopic ratios and radiocesium activity concentrations in flood sediment deposits collected in the Ukedo and Takase Rivers, draining a part of the Difficult-to-Return Zone, in Fukushima Prefecture, from 2013 to 2020. These radionuclides were released in large quantities during the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident that occurred in March 2011 in Northeastern Japan (Steinhauser et al., 2014). Models showed that ~ 80 % of radionuclide releases occurred over the ocean (Mathieu et al., 2018; MEXT, 2011). The radioactive plume is drained by several coastal rivers to the Pacific Ocean, and sediment-bound radionuclide transfers in these rivers are mainly controlled by the occurrence of typhoons and tropical storms (Evrard et al., 2021). The objective of the research relying on the current database is to investigate the temporal changes in Pu signatures that occurred between 2013 and 2020 in flood sediment deposits collected in the Ukedo and the Takase Rivers, and to identify potential factors controlling these changes by the means of statistical approach.</p> <p>The current dataset comprises an Excel file including the variables description, and the data itself.</p>
Рис.5. СоотношениеразΛичныхгнезΑовыхтиповопорв 2018–2019 гг. поаΑминистративным районам (Λевый график) и в цеΛом по Амурской обΛасти (правый график) Fig. 5. The ratio of different types of nesting supports in 2018–2019 by administrative districts (right graph) and in general in the Amur region (left graph) in Oriental stork (Ciconia boyciana Swinhoe) breeding population survey in the Amur region in 2018-2019
Рис.5. СоотношениеразΛичныхгнезΑовыхтиповопорв 2018–2019 гг. поаΑминистративным районам (Λевый график) и в цеΛом по Амурской обΛасти (правый график) Fig. 5. The ratio of different types of nesting supports in 2018–2019 by administrative districts (right graph) and in general in the Amur region (left graph)
Data from: Female-biased population sex ratios caused by genetic rather than ecological mechanisms in dwarf willow (Salix herbacea L.)
<p>Biased sex ratios among reproductive individuals are common in plants, but the underlying mechanisms, as well as the evolutionary consequences, are not well understood. The classical theory of Düsing and Fisher predicts an equal primary sex ratio at seed production, based on the selective advantage of the rare sex. Biased sex ratios among reproductive plants can arise from sexual dimorphism in survival and flowering. Sex ratio biases can also be present from the seed stage; in these cases, assumptions of Düsing's and Fisher's theory, for example, random mating or demographic equilibrium, are thought to be violated.</p> <p>We investigated mechanisms leading to female-biased sex ratios in the arctic-alpine dwarf willow <em>Salix herbacea</em> L. We studied sex ratios in three natural populations over three years as well as in 29 crosses (full-sib families) under controlled conditions over four growth periods. We tested whether sex ratio was associated with habitat parameters (elevation and snowmelt time), or with germination, survival or flowering, and whether females and males differed in size or flowering that may cause observation bias.</p> <p>We detected a strong and consistent female bias, both in natural populations (sex ratio [proportion of females]: 0.71-0.82) and in our controlled experiment (overall sex ratio: 0.70-0-72). Female bias became more pronounced with increasing elevation. Our data did not support sexual dimorphism in size or flowering. Family sex ratios varied largely (from 0.25 to 1), including many female-biased families, unbiased families and two male-biased families. Families with lower germination, seedling establishment, survival or flowering did not have stronger female bias, indicating that intrinsically higher survival or flowering in females does not explain overall female bias. </p> <p>Synthesis: Our results suggest that sex ratio bias in <em>S. herbacea</em> is already present in seeds and does not arise through intrinsic differences between sexes. Candidate mechanisms that can lead to both overall female bias and variation in sex ratio among families are meiotic drive or cyto-nuclear interactions. The pioneer habit of <em>Salix</em> may lead to non-equilibrium population dynamics that allow for the long-term persistence of variable genetic sex ratio distortion systems that arise from genetic conflict.</p>
An experimental dataset to explore the size ratio impact on an intruder segregating in bedload transport
<p>This repository gathers :</p> <ul> <li>The treated data used in the article "Exploring the size ratio impact on an intruder segregating in bedload transport" from Dedieu B., Rousseau H., Frey P. and Chauchat J. in Physical Review of Fluids (DOI: <a href="https://doi.org/10.1103/PhysRevFluids.9.104302" target="_blank" rel="noopener">10.1103/PhysRevFluids.9.104302</a>),</li> <li>Some re-computed data from the experiments of <a href="https://doi.org/10.1103/PhysRevFluids.7.064305" target="_blank" rel="noopener">Rousseau H. et al.(2022)</a> in csv format,</li> <li>A python3 package <em>codes</em> used to load the data.</li> </ul> <p>Explanations on how to use the codes and how the data are organized can be found in the <em>README.md</em>.</p> <p>Feel free to contact the authors if you need more information or wish to access the raw image data.</p>
Dataset for the publication: Impact of unintentionally formed CH2O in oxygenated fuel exhausts on DeNOx-SCR at different NO2/NOx ratios under close to real conditions
<p>The dataset covers the research data of the publication in Catalysis Science & Technology with the title "Impact of unintentionally formed CH2O in oxygenated fuel exhausts on DeNOx-SCR at different NO2/NOx ratios under close to real conditions" (DOI: 10.1039/d2cy01935c).</p>
Fig 1 in Growth performance of shrimp Litopenaeus vannamei under different carbon: Nitrogen (C/N) ratios of Bioflocs system
Fig 1: Growth Performance details – final weight and weight gain recorded in L.vannamei under different C/N ratios
Fig 4 in Growth performance of shrimp Litopenaeus vannamei under different carbon: Nitrogen (C/N) ratios of Bioflocs system
Fig 4: Growth Performance details – productivity rate recorded in L.vannamei under different C/N ratios
Fig 3 in Growth performance of shrimp Litopenaeus vannamei under different carbon: Nitrogen (C/N) ratios of Bioflocs system
Fig 3: Growth Performance details – Gross Feed Conversion Efficiency (GFCE) recorded in L.vannamei under different C/N ratios
Fig 2 in Growth performance of shrimp Litopenaeus vannamei under different carbon: Nitrogen (C/N) ratios of Bioflocs system
Fig 2: Growth Performance details – Specific Growth Rates (SGR) and Feed Conversion Ratio (FCR) recorded in L.vannamei under different C/N ratios
FIG. 5 in Expressed sex ratio in populations of the moss Hamatocaulis vernicosus (Mitt.) Hedenäs (Scorpidiaceae) in the Czech Republic with consideration of its cryptic species
FIG. 5. — The sex ratio in mixed population at locality Zhůří 1. Unbordered pie charts refer to clade 1, bordered ones represent clade 2. The patch in the larger circle contained plants of both clades, so this patch must be excluded from evaluating sex ratio in separated clades.
FIG. 3 in Expressed sex ratio in populations of the moss Hamatocaulis vernicosus (Mitt.) Hedenäs (Scorpidiaceae) in the Czech Republic with consideration of its cryptic species
FIG. 3. — Rates of male (blue), female (red) and non-expressing (green) plants at studied localities of Hamatocaulis vernicosus (Mitt.) Hedenäs clade 1 and 2.
FIG. 2 in Expressed sex ratio in populations of the moss Hamatocaulis vernicosus (Mitt.) Hedenäs (Scorpidiaceae) in the Czech Republic with consideration of its cryptic species
FIG. 2. — The expressed sex ratio at studied localities of H. vernicosus (Mitt.) Hedenäs. In mixed populations,only single-clade patches were used for the assessment.
FIG. 4 in Expressed sex ratio in populations of the moss Hamatocaulis vernicosus (Mitt.) Hedenäs (Scorpidiaceae) in the Czech Republic with consideration of its cryptic species
FIG. 4.— Sex ratio at localities with co-occurring cryptic species. All, without distinguished clades; cl. 1, clade 1; cl. 2, clade 2; Šimanov, Šimanovské rašeliniště. Only barcoded shoots were used to create this graph.
FIG. 1 in Expressed sex ratio in populations of the moss Hamatocaulis vernicosus (Mitt.) Hedenäs (Scorpidiaceae) in the Czech Republic with consideration of its cryptic species
FIG. 1.— The sex expression of Hamatocaulis vernicosus (Mitt.) Hedenäs in the Czech Republic at individual localities assessed at two levels of pooling hierarchy ("shoots at localities" and "patches at localities").
Data for "Bar to bank height ratio sets bank erosion rate"
<p>CaseA1_Q20Zbar15Zbank35_initial.csv ~ CaseB6_Q30Zbar45Zbank45_last.csv: Survey data of riverbed topography at the beginning of the experiment (_initial.csv) and at the end of the experiment (_last.csv). The first line of each file indicates the number of measurement points, and the second and subsequent lines indicate the x, y, and z coordinates.</p> <p>velocity results.zip: Results of flow velocity analysis using iRIC Nays2DH. The ipro files stored in the zip can be opened by installing the free software "iRIC" (https://i-ric.org/en/). Please refer to the manual and the examples (https://i-ric.org/en/solvers/nays2dh/) for how to view calculation results and calculation conditions.</p> <p>bar height and near bank velocity.xlsx: Table on bar height and near-bank velocity for each case.</p> <p> </p>
Fig. 1 in Preliminary data on adult sex-ratio in Phyllognathus excavatus (Coleoptera: Scarabaeidae) in central Italy
Fig. 1. Daily sex-ratio variations of adult Phyllognathus excavatus (Forster, 1771) in Lavinio, central Italy. For statistical details, see the text. Sample sizes: July 21 = 16, July 22 = 22, July 23 = 4, July 26 = 6, July 27 = 0, August 9-10 = 0, September 5 = 5 (two outside the transects)
Appendix A. Supplementary material for: Water-like thermal conductivity of ionanofluids containing high aspect ratio multi-walled carbon nanotubes and 1-ethyl-3-methylimidazolium-based ionic liquids with cyano-functionalized anions
<p><span>Experimental data in numerical form for INFs composed of CNTs and [Emim]-based ILs with cyano-functionalized anions: density (Table S1), viscosity (Tables S2–S5), thermal conductivity (Tables S6, S7), and ANOVA analysis (Table S8).</span></p>
Figs 3–4. 3 in Seasonal Changes In The Sex Ratio Of Nyctalus Species In North-East Hungary
Figs 3–4. 3 = The numbers of males and females of N. lasiopterus grouped into 15 day periods. 4 = Sex ratios of N. leisleri in different parts of Europe [source: 1 (HELVERSEN & WEID); 2 (GAISLER 1975); 3 (HEISE 1982); 4 (LICHACEV 1980); 5 (ABELENCEV et al. 1956) in BOGDANOWICZ & RUPRECHT 2004]
Associated data for "The Roasting Marshmallows Program with IGRINS on Gemini South II -- WASP-121 b has super-stellar C/O and refractory-to-volatile ratios" Published in The Astronomical Journal
<table> <tbody> <tr> <td>File Name</td> <td>Description</td> </tr> <tr> <td>w121_1DRC_H2O_ONLY.txt</td> <td>Self consistent, solar composition model spectrum with only H2O opacity.</td> </tr> <tr> <td>w121_1DRC_OH_ONLY.txt</td> <td>Self consistent, solar composition model spectrum with only OH opacity.</td> </tr> <tr> <td>w121_1DRC_CO_ONLY.txt</td> <td>Self consistent, solar composition model spectrum with only CO opacity.</td> </tr> <tr> <td>w121_1DRC_EVERYTHING.txt</td> <td>Self consistent, solar composition model spectrum with all sources of opacity.</td> </tr> <tr> <td>pre_.pic</td> <td>Pre-eclipse data in data cuboid of shape N_order, N_frame, N_pixel</td> </tr> <tr> <td>pre_variance.pic</td> <td>Associated per-pixel variance for the pre-eclipse data.</td> </tr> <tr> <td>post_cube.pic</td> <td>Post-eclipse data in data cuboid of shape N_order, N_frame, N_pixel</td> </tr> <tr> <td>pre_time_BJD.pic</td> <td>Average frame time in BJD for the pre-eclipse sequence.</td> </tr> <tr> <td>pre_rvel.pic</td> <td>Stellar radial velocity, including barycentric correction, per frame for the pre-eclipse sequence.</td> </tr> <tr> <td>post_ph.pic</td> <td>Orbital phase per frame for the post-eclipse sequence.</td> </tr> <tr> <td>post_time_BJD.pic</td> <td>Average frame time in BJD for the post-eclipse sequence.</td> </tr> <tr> <td>post_rvel.pic</td> <td>Stellar radial velocity, including barycentric correction, per frame for the post-eclipse sequence</td> </tr> </tbody> </table>
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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)
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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.