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6,175 results for “composite”
AMBON diversity & community composition, data & code
<p>Data and R code for analyzing diversity and community composition of eight assemblages in the Northeast Chukchi Sea in 2015 and 2017. For details of the analysis, results and interpretation, see:</p> <p><em>Mueter, F.J., Iken, K., Cooper, L.W., Grebmeier, J.M., Kuletz, K.J., Hopcroft, R.R., Danielson, S.L., Collins, R.E., Cushing, D. Changes in diversity and species composition across multiple assemblages in the northeast Chukchi Sea during two contrasting years are consistent with borealization. Oceanography (In Press).</em></p>
Morpho-anatomical traits explain the effects of bacterial-feeding nematodes on soil bacterial community composition and plant growth and nutrition
<p>Soil Bacterial populations</p> <p>V3-V4, of the 16S rRNA gene using the primers 341F CCTAYGGGRBGCASCAG and 806R GGACTACNNGGGTATCTAAT.</p>
Data and code from "Water availability is a stronger driver of soil microbial processing of organic nitrogen than tree species composition"
<p>#### Data description<br> Data from large scale, long-term tree diversity experiment in southwestern France (<a href="https://sites.google.com/view/orpheeexperiment/home">ORPHEE</a>), additionally manipulating water contraint. Variables presented are soil nitrogen cycling rates measured using isotope pool dilutions.</p> <p>Companion paper is found here:</p> <p>Maxwell TL, Augusto L, Tian Y, Wanek W & Fanin N (2023). Water availability is a stronger driver of soil microbial processing of organic nitrogen than tree species composition. <em>European Journal of Soil Science</em>. <a href="https://doi.org/10.1111/ejss.13350">https://doi.org/10.1111/ejss.13350</a></p> <p>#### Metadata<br> Soil sampling: July 2020<br> Maxwell_ShortComm_Data.csv data description</p> <p>ID: unique identifier per sample<br> Block: numbered 1-6. Blocks 1,3,6 are control (unirrigated), Blocks, 2,4,5 are irrigated<br> Plot: numbered plot according to the ORPHEE design. Plot 1 = BP, Plot 5 = PP, Plot 9 = BP_PP<br> Espece: species ID. BP = pure birch (<em>Betula pendula</em>), PP = pure pine (<em>Pinus pinaster</em>), BP_PP (50% mixed birch-pine)<br> Rep: sample replicate, 3 replicates per plot<br> Sample name: long unique identifier per sample. Concatenation of Block, Plot, and Espece<br> PD: gross protein depolymerization rates (micrograms nitrogen per grams dry soil per day = µg N g-1 d-1)<br> AAU: gross free amino acid uptake rates (µg N g-1 d-1)<br> Cmicrobial_ug_g: microbial biomass carbon (µg C g-1)<br> Nmicrobial_ug_g: microbial biomass nitrogen (µg N g-1)<br> MRT_FAA_hrs: mean residence time of free amino acids (hours)<br> FAA_ugN_g: free amino acids (µg N g-1)<br> Moisture_percent: soil moisture percent (%)<br> N_nonfumige_ug_g: nitrogen from non fumigated soils, i.e. extractable N (µg N g-1)<br> C_nonfumige_ug_g: nitrogen from non fumigated soils, i.e. extractableC (µg C g-1)</p>
Data set for the journal article: Colloidal-ALD Grown Metal Oxide Shells Enable the Synthesis of Photoactive Ligand/ Nanocrystal Composite Materials
<p>The data for each figure of the main manuscript is included in this folder.</p> <p>Figure 1 is not included as it contains no data.</p> <p>The folder for Figure 2 contains a sub-folder for the EDX and NMR data of 9-ACA/PbS@AlOx. The NMR data was processed by Mestrenova.</p> <p>The folder for Figure 3 contains optical absorption spectrum data of 9-ACA/PbS@AlOx.</p> <p>The folder for Figure 4 contains NMR data which was processed by Mestrenova. It contains the data for 9-ACA/CuInS2@AlOx, 1-PCA/CsPbBr3@AlOx and 9-PTA/CsPbBr3@AlOx.</p> <p>The folder for Figure 5 is made of three sub-folders for figure 5A, 5B and 5C. 5A and 5B contain optical absorption for the CuInS2 and CsPbBr3 datasets while 5C contain time resolved data for CsPbBr3.</p> <p>The folder for Figure 6 contains time resolved PL for the as synthesized CsPbBr3, 1-PCA/CsPbBr3@AlOx and 9-PTA/CsPbBr3@AlOx. The 9-PTA/CsPbBr3@AlOx data contain two decays that span 200 ns (short) or 13.5 us (long).</p> <p>The folder for Figure 7 contains time resolved PL for the as synthesized 9-PTA/CsPbBr3@AlOx and 1-PCA/9-PTA/CsPbBr3@AlOx. For both samples the data contain two decays that span 200 ns (short) or 13.5 us (long). Also an NMR folder is present with the 1H spectrum for 9-PTA/CsPbBr3@AlOx and 1-PCA/9-PTA/CsPbBr3@AlOx.</p> <p> </p> <p> </p>
Solar Wind properties measured with instruments on the Advanced Composition Explorer (ACE)
<p>Combined ACE/SWEPAM, ACE/Mag, and ACE/SWICS data set<br> ACE/MAG and ACE/SWEPAM data are taken from the ACE Science center (https://izw1.caltech.edu/ACE/ASC/) and binned to the 12-minute time resolution of SWICS.<br> The SWICS data is based on the PHA data and analyzed as described in Berger (2008).<br> This data set is used in the following two publications:<br> Teichmann, S. Heidrich-Meisner, V, Berger, L, Wimmer-Schweingruber, R.F. (2023, submitted), "Influence of solar wind parameters on unsupervised solar wind classification with k-means" source code available: 10.5281/zenodo.7695074<br> Hecht, M, Heidrich-Meisner, V, Berger, L, Wimmer-Schweingruber, R.F. 2023 (in preparation) "Scope and limitations of ad-hoc neural network reconstructions of solar wind parameters", source code available: 10.5281/zenodo.7681047.</p> <p>Contact: Verena Heidrich-Meisner, CAU Kiel heidrich@physik.uni-kiel.de</p> <p>We thank the science teams of ACE/SWEPAM, ACE/MAG as well as<br> ACE/SWICS for developing, maintaining and calibrating the instruments and for providing the respective level 2 and level 1 data products.<br> This work was supported by the Deutsches Zentrum für Luft- und Raumfahrt (DLR) as SOHO/CELIAS 50 OC 2104.</p> <p>Data products description:<br> year: year of observation (int)<br> time: day of year in current year as float<br> yeartime: time in years as float (UTC)<br> vsw: solar wind proton speed in km/s, measured by ACE/SWEPAM (level 2 from ACE Science Center) and rebinned to 12 minute time resolution<br> dsw: solar wind proton density in cm^{-3}, measured by ACE/SWEPAM (level 2 from ACE Science Center)and rebinned to 12 minute time resolution<br> tsw: solar wind proton temperature in K, measured by ACE/SWEPAM (level 2 from ACE Science Center) and rebinned to 12 minute time resolution<br> B: magnetic feld strength in nT, measured by ACE/MAG (level 2 from ACE Science Center)<br> colage: proton-proton collisional age computed as 6.4* 1e8 * dsw /(vsw* tsw**(3/2)) in K^{3/2} s^2 cm^3 km^{-1}<br> dO7_6: ratio of the O7+ to O6+ charge state densities, measured by ACE/SWICS, derived directly from PHA (pulse height analysis) data<br> eO7_6: estimate of the relative error of dO7_6 based on the counting statistics<br> ldO7_6: decadic logarithm of dO7_6<br> elO7_6: estimate of the relative error of the decadic logarithm dO7_6 based on the counting statistics<br> mcsFe: mean charge state of Fe, based on SWICS PHA of Fe8+, Fe9+, Fe10+, Fe11+, and Fe12+ in units of the elementary charge e. At least 10 counts distributed over Fe8+, Fe9+, Fe10+, Fe11+ and Fe12+ are required<br> emcsFe: estimate of the relative error of dO7_the mean Fe charge state in e (assumes 10% relative error for each Fe charge state)<br> cor_hole: coronal hole wind category in the categorization of Xu&Borovsky (2015) The ejecta category is disregarded, see for example Heidrich-Meisner (2020). Entries are 0 or 1, 1 of the data point is assigned to this type.<br> sec_rev: sector reversal plasma wind category in the categorization of Xu&Borovsky (2015) The ejecta category is disregarded, see for example Heidrich-Meisner (2020). Entries are 0 or 1, 1 of the data point is assigned to this type.<br> stream_belt: streamer belt wind category in the categorization of Xu&Borovsky (2015) The ejecta category is disregarded, see for example Heidrich-Meisner (2020). Entries are 0 or 1, 1 of the data point is assigned to this type.<br> ICME: interplanatery coronal mass ejections time periods (with a six hour safety margin before and after each ICME) from the Jian (2006,2011) and Richardson & Cane (2014, 2018) ICME lists. Entries are 0 or 1, 1 of the data point is assigned to this type.<br> totalCountsFe: number of counts in ACE/SWICS distributed over Fe8+-Fe12+<br> The data set is restricted to data points where valid data points are available for all listed data products. Only for the mean charge state of Fe invalid data points are indicated with nan (not a number)</p> <p>References:<br> Berger, L. 2008, PhD thesis, Kiel, Christian-Albrechts-Universität, Diss., 2008<br> Gloeckler, G., Cain, J., Ipavich, F., et al. 1998, in The Advanced Composition Explorer Mission (Springer), 497–539<br> McComas, D., Bame, S., Barker, P., et al. 1998b, in The Advanced Composition Explorer Mission (Springer), 563–612<br> Smith, C. W., L’Heureux, J., Ness, N. F., et al. 1998, in The Advanced Composition Explorer Mission (Springer), 613–632</p> <p>Xu, F. & Borovsky, J. E. 2015, Journal of Geophysical Research: Space Physics, 120, 70<br> Heidrich-Meisner, V., Berger, L., & Wimmer-Schweingruber, R. F. 2020, Astronomy & Astrophysics, 636, A103<br> Jian, L., Russell, C., & Luhmann, J. 2011, Solar Physics, 274, 321<br> Jian, L., Russell, C., Luhmann, J., & Skoug, R. 2006, Solar Physics, 239, 393<br> Richardson, I. G. 2004, Space Science Reviews, 111, 267<br> Richardson, I. G. 2018, Living reviews in solar physics, 15, 1</p> <p>Teichmann, S. Heidrich-Meisner, V, Berger, L, Wimmer-Schweingruber, R.F. (2023), "Influence of solar wind parameters on unsupervised solar wind classification with k-means" source code available: 10.5281/zenodo.7695074<br> Hecht, M, Heidrich-Meisner, V, Berger, L, Wimmer-Schweingruber, R.F. 2023 (in preparation) "Scope and limitations of ad-hoc neural network reconstructions of solar wind parameters", source code available: 10.5281/zenodo.7681047.</p> <p>year/1 time/day of year yeartime/UTC vsw/km/s dsw/cm^{-3} tsw/K B/nT colage/(K^{3/2} s^2 cm^3 km^{-1}) dO7_6/1 eO7_6/1 ldO7_6/1 elO7_6/1 mcsFe/e emcsFe/e cor_hole/bool sec_rev/bool stream_belt/bool ICME/bool totalCountsFe/1</p>
Micro elemental composition of Pike-perch (Sander lucioperca) population in Lipno Reservoir, Czechia
<p>This dataset contains the information on the micro elemental composition of Sagitta otoliths of Pike-Perch (<i>Sander lucioperca</i>) collected in Lipno Reservoir (Czechia). The dataset covers a wide range of micro elemental components (barium, calcium, copper, potassium, lithium, magnesium, manganese, sodium, rubidium, strontium and zinc) obtained from the otolith cores and rims of these fish specimens. The dataset includes readings from Pike-Perch directly collected in Lipno Reservoir, as well as from those reared in facilities and later introduced into the reservoir.</p>
Summer water chemistry, phytoplankton and zooplankton community composition, size structure, and biomass in a shallow, hypereutrophic reservoir in southwestern Iowa, USA (2019).
This data product contains data for Green Valley Lake, a hypereutrophic reservoir in southwest Iowa (USA) from the summer of 2019. We sampled and quantified zooplankton, phytoplankton, and nutrient concentrations (total N, total P, soluble reactive P, nitrate) in the lake weekly with the primary aim of assessing consumer nutrient cycling, specifically zooplankton nutrient cycling, in a hypereutrophic reservoir. Weekly plankton sampling included quantifying zooplankton and phytoplankton biomass, community composition, and size structure. Phytoplankton size was measured as the greatest axial linear distance which would be approached by a zooplankton grazer. Allometric equations from the literature were applied to the zooplankton size measurements to estimate zooplankton community excretion of N and P. We found that the estimated contribution of zooplankton excretion to the dissolved P pool was substantial in the spring. Further, we found evidence that zooplankton affected phytoplankton size distributions through selective grazing of smaller phytoplankton cells likely affecting nutrient uptake and storage by phytoplankton.
Linking temporal changes in species composition and biomass in a globally distributed grassland experiment: The Nutrient Network
Global change drivers, such as anthropogenic nutrient inputs, are increasing globally. Nutrient deposition simultaneously alters plant biodiversity, species composition, and ecosystem processes like aboveground biomass production. These changes are underpinned by species extinction, colonization, and shifting relative abundance. Here, we use the Price equation to quantify and link the contributions of species that are lost, gained, or that persist to change in aboveground biomass in 59 experimental grassland sites. Under ambient (control) conditions, compositional and biomass turnover was high, and losses (i.e., local extinctions) were balanced by gains (i.e. colonization). Under fertilization, the decline in species richness resulted from increased species loss and from decreases in species gained. Biomass increase under fertilization resulted mostly from species that persist, and to a lesser extent from species gained. Drivers of ecological change can interact relatively independently with diversity, composition, and ecosystem processes and functions such as aboveground biomass due to the individual contributions of species lost, gained, or persisting.
The recovery of plant community composition following passive restoration across spatial scales, Cedar Creek Ecosystem Science Reserve, 1983-2016
1. Human impacts have led to dramatic biodiversity change which can be highly scale-dependent across space and time. A primary means to manage these changes is via passive (here, the removal of disturbance) or active (management interventions) ecological restoration. The recovery of biodiversity, following the removal of disturbance is often incomplete relative to some kind of reference target. The magnitude of recovery of ecological systems following disturbance depend on the landscape matrix, as well as the temporal and spatial scales at which biodiversity is measured. 2. We measured the recovery of biodiversity and species composition over 27 years in 17 temperate grasslands abandoned after agriculture at different points in time, collectively forming a chronosequence since abandonment from one to eighty years. We compare these abandoned sites with known agricultural land-use histories to never-disturbed sites as relative benchmarks. We specifically measured aspects of diversity at the local plot-scale (α-scale, 0.5m2) and site-scale (γ-scale, 10m2), as well as the within-site heterogeneity (β-diversity) and among-site variation in species composition (turnover and nestedness). 3. At our α-scale, sites recovering after agricultural abandonment only had 70% of the plant species richness (and ~30% of the evenness), compared to never-ploughed sites. Within-site β-diversity recovered following agricultural abandonment to around 90% after 80 years. This effect, however, was not enough to lead to recovery at our γ-scale. Richness in recovering sites was ~65% of that in remnant never-ploughed sites. The presence of species characteristic of the never disturbed sites increased in the recovering sites through time. Forb and legume cover declines in years since abandonment, relative to graminoid cover across sites. 4. Synthesis. We found that, during the 80 years after agricultural abandonment, old-fields did not recover to the level of biodiversity in remnant never-plough
Submersed aquatic vegetation community composition in the Sacramento-San Joaquin Delta integrated across four surveys
Submersed aquatic vegetation (SAV) has become widespread in the Sacramento-San Joaquin Delta (Delta), and the diverse SAV assemblage is dominated by non-native species. SAV negatively impacts this estuarine ecosystem by impeding flows needed for water delivery and flood control, degrading habitat needed by native species, increasing breeding habitat for disease-vectoring mosquitoes, harboring non-native predatory fish, and hindering water recreation. The goal of this published integrated dataset is to facilitate study of these impacts. This data set includes four surveys conducted in the region during 2008-2021. Two of these are short-term special studies that have been completed, and two are ongoing long-term annual surveys. The nearshore survey of SAV and largemouth bass was conducted by the University of California-Davis (UC-Davis) at sites across the Delta during 2008-2010. The Aquatic Weed Control Action was completed by the Department of Water Resources as part of the Delta Smelt Resiliency Strategy and included monthly surveys of four sites during 2017-2018. The ongoing survey of Franks Tract is conducted annually by the SePRO corporation and the Division of Boating and Waterways, and available data are from 2014-2021. The ongoing annual survey conducted by the UC-Davis Center for Spatial Technologies and Remote Sensing covers many areas of the Delta and spans 2007-2008 and 2014-2021. Additional data from these ongoing surveys and data from other surveys will be added in subsequent versions of this data set.
PVC02 Plant species composition on selected watersheds at Konza Prairie (Reformatted to the ecocomDP Design Pattern)
This data package is formatted as an ecocomDP (Ecological Community Data Pattern). For more information on ecocomDP see https://github.com/EDIorg/ecocomDP. This Level 1 data package was derived from the Level 0 data package found here: https://pasta.lternet.edu/package/metadata/eml/knb-lter-knz/69/18. The abstract below was extracted from the Level 0 data package and is included for context: Canopy coverage and frequency were recorded in 20 circular 10 sq m plots. Six treatments were sampled, three ungrazed and three to grazed by native grazers. In each case one of the three watersheds was unburned, another burned annually in April, the third burned every four years in April. In each treatment two soils were sampled: a lower-slope deep fertile nonrocky soil (tully silty clay loam), and a shallow rocky soil (florence cherty silt loam) on level to gently sloping ridges. In 1983 another ungrazed annual burn area '1c' was added 'both tully and florence soils' because original area '1d' appeared aberrant.
Crossing Treeline: Bacterioplankton community composition in alpine and subalpine lakes of the Rocky Mountain southern ecoregion and associated physical and chemical characteristics
This dataset includes lake water samples collected in the summer of 2016 from 16 different mountain lakes in the Rocky mountains in both Rocky Mountain National Park and the Snowy Range of southern Wyoming. Each lake was sampled twice: once in the early summer when hydrologic connections with the surrounding terrestrial environment were high and again in the late summer when hydrologic connections were low. The main goal of the study was to compare communities of bacterioplankton in alpine and subalpine lakes to determine if communities differed across treeline as soil microbes in the surrounding terrestrial environment were. To do so, we collected water samples from the deepest point of each lake, mixed it with a surface water sample and characterized bacterioplankton communities with 16S sequencing technology. Additionally, we wanted to identify abiotic factors that may correlate with community dissimilarity and characterized a suite of chemical attributes for each lake. Lake characteristics reported included surface temperature, soluble reactive phosphorous (SRP), ammonia (NH3+), pH, total dissolved nitrogen (TDN), total dissolved phosphorus (TDP), and total dissolved organic carbon (DOC), and chlorophyll a (chl-a).
Composition and biolability of dissolved organic matter from arctic and boreal streams April 2015 - May 2016
In this study, we collected samples throughout the year from up to eight streams along an arctic-boreal gradient in interior Alaska, ranging from discontinuous to continuous permafrost. We measured dissolved organic matter (DOM) biolability and nutrient limitation of decomposition through laboratory incubations of streamwater, and characterized DOM composition through optical properties and chemical analysis.
Pre and post-fire composition, density, basal area, and biomass for 212 sites that burned between 2004 and 2015 in Interior Alaska
We collated data on pre-fire and post-fire stand composition from 212 sites across interior Alaska that burned between the years 2004 and 2014.
Temporal and spatial changes of the abundance and species composition of phytoplankton in the California Current from samples collected aboard CalCOFI cruises from summer 1996 through 2022.
The abundances of 385 taxonomic categories of phytoplankton (species where possible) are presented for the 26.5 -year period beginning with summer, 1996 and concluding with autumn 2022. There were four cruises per year. Samples were water samples collected from the second depth, which was designed to sample the mixed layer when a mixed layer existed, generally between 5m - 15m. Before counting, samples from single stations were pooled into four regions: NE (northern inshore), SE (southern inshore), Alley (the region of the California Current) and Offshore (Central Pacific). Pooled samples were enumerated with an inverted microscope. The species data are presented by seven major taxonomic categories followed by the sums of those major taxa. The species codes are defined in the table metadata.
Tree mortality in Forest and Biodiversity 2: a tree diversity experiment to understand the consequences of multiple dimensions of diversity and composition for long-term ecosystem function and resilience
The Forest and Biodiversity (FAB2) experiment uses native tree species in varying levels of species richness, phylogenetic diversity, and functional diversity planted in 100 m2 and 400 m2 plots at 1 m spacing, appropriate for testing long-term ecosystem consequences. FAB2 was designed and established in conjunction with a prior experiment (FAB1) in which the same set of twelve species was planted in 16 m2 plots at 0.5 m spacing. Both are adjacent to the BioDIV prairie-grassland diversity experiment, enabling comparative investigations of diversity and ecosystem function relationships between experimental grasslands and forests at different planting densities and plot sizes. This data package examines mortality in the first six years of the experiment.
FAB2_sapling_volume_2021-2022 in Forest and Biodiversity 2: a tree diversity experiment to understand the consequences of multiple dimensions of diversity and composition for long-term ecosystem function and resilience
The Forest and Biodiversity (FAB2) experiment uses native tree species in varying levels of species richness, phylogenetic diversity, and functional diversity planted in 100 m2 and 400 m2 plots at 1 m spacing, appropriate for testing long-term ecosystem consequences. FAB2 was designed and established in conjunction with a prior experiment (FAB1) in which the same set of twelve species was planted in 16 m2 plots at 0.5 m spacing. Both are adjacent to the BioDIV prairie-grassland diversity experiment, enabling comparative investigations of diversity and ecosystem function relationships between experimental grasslands and forests at different planting densities and plot sizes. This data package examines mortality in the first six years of the experiment.
fab2_allometry_2016-2022 in Forest and Biodiversity 2: a tree diversity experiment to understand the consequences of multiple dimensions of diversity and composition for long-term ecosystem function and resilience
The Forest and Biodiversity (FAB2) experiment uses native tree species in varying levels of species richness, phylogenetic diversity, and functional diversity planted in 100 m2 and 400 m2 plots at 1 m spacing, appropriate for testing long-term ecosystem consequences. FAB2 was designed and established in conjunction with a prior experiment (FAB1) in which the same set of twelve species was planted in 16 m2 plots at 0.5 m spacing. Both are adjacent to the BioDIV prairie-grassland diversity experiment, enabling comparative investigations of diversity and ecosystem function relationships between experimental grasslands and forests at different planting densities and plot sizes. This data package examines mortality in the first six years of the experiment.
Forest composition and diversity buffer microclimates and enhance productivity
The Forest and Biodiversity (FAB2) experiment uses native tree species in varying levels of species richness, phylogenetic diversity, and functional diversity planted in 100 m2 and 400 m2 plots at 1 m spacing, appropriate for testing long-term ecosystem consequences. FAB2 was designed and established in conjunction with a prior experiment (FAB1) in which the same set of twelve species was planted in 16 m2 plots at 0.5 m spacing. Both are adjacent to the BioDIV prairie-grassland diversity experiment, enabling comparative investigations of diversity and ecosystem function relationships between experimental grasslands and forests at different planting densities and plot sizes. This data package examines mortality in the first six years of the experiment. This data package examines the relationships between forest biodiversity, forest structure, microclimates, leaf-level physiology, and tree growth. A wide variety of data types are included, such as metrics of tree diversity, UAV-LiDAR metrics, spectral indices, microclimate data, gas exchange measurements, and tree growth inventories. This data package is included in the submission of the manuscript entitled “Forest composition and diversity buffer microclimates and enhance productivity.”
Environmental and periphyton composition data from Biscayne Bay Coastal Wetlands, Florida, USA, July 2022 - November 2022
Environmental and periphyton data were collected from transects in the Biscayne Bay Coastal Wetlands (BBCW) during the wet and dry seasons of 2022 to investigate the rate of carbonate sediment production by periphyton. Environmental data include surface water metrics (pH, salinity, conductivity, and water depth) and soil depths. Periphyton data include nutrient, production, and diatom species composition in samples collected from artificial substrates (periphytometers) placed in the field. Data collection for this project is complete, although the South Florida Management District continues to monitor these transects for a larger ongoing BBCW project.
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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.