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Maps of depths are created for the site of 50 m length. Flow types are turbulent, broken standing waves, unbroken standing waves, and rippled. The average width was 8 m and varied from 5.5 to 12 m. Bed elements included bars, rocks, and step/pools. The average depth was 0.35 m, with a maximum of 0.6 m. The average velocity was 0.4 m/s, with a maximum of 1.2 m/s (figs 10). Distribution of bottom habitats at the locations with the crayfish are as follows: megalital — 5 %, macrolithal — 30 %, mesolithal — 25 %, microlithal — 15 %, psammal — 15 %, CPOM — 10 %. Assessment by hydrobiological parameters showed that the presence of Lyngbya and Oscillatoria, as well as the increase of the number of Oligochae- in New Findings Of White Clawed Crayfish, Austropotamobius Pallipes (Decapoda, Astacidae), And Peculiarities Of Its Spatial Distribution In Neretvica (Bosnia And Herzegovina)
Maps of depths are created for the site of 50 m length. Flow types are turbulent, broken standing waves, unbroken standing waves, and rippled. The average width was 8 m and varied from 5.5 to 12 m. Bed elements included bars, rocks, and step/pools. The average depth was 0.35 m, with a maximum of 0.6 m. The average velocity was 0.4 m/s, with a maximum of 1.2 m/s (figs 10). Distribution of bottom habitats at the locations with the crayfish are as follows: megalital — 5 %, macrolithal — 30 %, mesolithal — 25 %, microlithal — 15 %, psammal — 15 %, CPOM — 10 %. Assessment by hydrobiological parameters showed that the presence of Lyngbya and Oscillatoria, as well as the increase of the number of Oligochae-
Fig. 4 in New Findings Of White Clawed Crayfish, Austropotamobius Pallipes (Decapoda, Astacidae), And Peculiarities Of Its Spatial Distribution In Neretvica (Bosnia And Herzegovina)
Fig. 4. Habitat with the highest concentration of the crayfish in Neretvica at the confluence with the Crni Potok.
Black Hole and White Hole Time Dilation
<p>This signifies the start of the experimental observation series on the white hole. The visibility of the Small Magellanic Cloud is based on the strong force's resonance effect, and is exemplified by the video. The M87 video mimics the shockwave arrival time via signal noise processing. The CMB is seen as a forward progress of time. The two phases of the moon by radiation are respectively from white hole and black hole's radiative processes on the sun and the moon.</p>
Balancing carnivore conservation and sustainable hunting of a key prey species: a case study on the Florida panther and white-tailed deer
<p>1. Large carnivore restoration programs are often promoted as capable of providing ecosystem services. However, these programs rarely measure effects of successful restoration on other economically and ecologically important species. In South Florida, while the endangered Florida panther (Puma concolor coryi) population has increased in recent years due to conservation efforts, the population of its main prey, the white-tailed deer (Odocoileus virginianus), has declined in some regions. The extent to which panther predation has affected deer populations has been difficult to assess because several other factors have changed during this period, including hydrology and hunting regulations.</p> <p>2. We collected known-fate survival data on 241 GPS-collared adult deer (156 females and 85 males) from 2015 to 2018 in the Florida Panther National Wildlife Refuge and the Big Cypress National Preserve in Florida, USA, to assess effects of panther predation on the deer population, while also evaluating the impacts of hunting and hydrology.</p> <p>3. Predation was the primary cause of death (110 of 134 mortalities), and 87% of predation events were attributed to panthers, a much greater rate than reported by studies conducted before the panther genetic restoration effort initiated in 1995. One deer was legally harvested, and two were likely killed by poachers. Increasing water depth decreased female survival but had little impact on male survival, and drowning was never a cause of mortality.</p> <p>4. Females had greater survival probability than males, except during fawning season. From 2015 to 2018, annual survival rates increased from 0.61 (0.52-0.70) to 0.86 (0.79-0.91) for females, and from 0.45 (95% CI: 0.33-0.58) to 0.79 (0.69-0.86) for males.</p> <p>5. Synthesis and applications – High predation rates, coupled with previous evidence of low recruitment of deer in South Florida, suggest that it will be challenging to meet society's competing demands for large predator restoration and sustainable deer harvest. Deer hunting in the area must remain tightly controlled, for now, if it is to be sustainable, and managers should seek to mitigate effects of high waters and improve deer habitat quality to increase deer population viability. Future work should closely monitor the deer population to assess if management actions can increase vital rates and abundance in the context of high predation rates.</p>
A gap in the double white dwarf separation distribution caused by the common-envelope evolution: astrometric evidence from Gaia
<p>Here we provide a supplementary dataset to our publication <em>A gap in the double white dwarf separation distribution caused by the common-envelope evolution: astrometric evidence from Gaia,</em> <a href="https://arxiv.org/abs/2203.03659">arXiv:2203.03659</a>. The dataset consists of 119 double white dwarf candidates selected in the Gaia Early Data Release 3 (EDR3) based on the sources' astrometric wobble amplitude. For each candidate we provide sky coordinates (RA, DEC), Gaia EDR3 ID, position on the HR diagram (G, BP-RP) and estimated astrometric wobble amplitude (delta a). Note that the astrometric wobble amplitude (delta a) is directly related to the binary’s orbital separation, as detailed in our paper.</p>
wGrapeUNIPD-DL: an open dataset for white grape bunch detection
<p>National and international Vitis variety catalogues can be used as image datasets for computer vision in viticulture. These databases archive ampelographic features and phenology of several grape varieties and plant structures images (e.g. leaf, bunch, shoots). Although these archives represent a potential database for computer vision in viticulture, plant structure images are acquired singularly and mostly not directly in the vineyard. Localization computer vision models would take advantage of multiple objects in the same image, allowing more efficient training. The present images and labels dataset was designed to overcome such limitations and provide suitable images for multiple cluster identification in white grape varieties. A group of 373 images were acquired from later view in vertical shoot position vineyards in six different Italian locations at different phenological stages. Images were then labelled in YOLO labelling format. The dataset was made available both in terms of images and labels. The real number of bunches counted in the field, and the number of bunches visible in the image (not covered by other vine structures) was recorded for a group of images in this dataset.</p>
Ecoregion and community structure influences on the foliar elemental niche of balsam fir (Abies balsamea (L.) Mill.) and white birch (Betula papyrifera Marshall)
<p><strong><span>Context</span></strong><span>: Changes in foliar elemental niche properties, defined by axes of carbon (C), nitrogen (N), and phosphorus (P) concentrations, reflect how species allocate resources under different environmental conditions. For instance, elemental niches may differ in response to large-scale latitudinal temperature and precipitation regimes that occur between ecoregions and small-scale differences in nutrient dynamics based on species co-occurrences at a community level.</span></p> <p><strong><span>Methods</span></strong><span>: at a species level, we compared foliar elemental niche hypervolumes for balsam fir (<em>Abies balsamea</em> (L.) Mill.) and white birch (<em>Betula papyrifera</em> Marshall) between a northern and southern ecoregion. At a community level, we grouped our focal species using plot data into conspecific (i.e., only one focal species is present) and heterospecific groups (i.e., both focal species are present) and compared their foliar elemental concentrations under these community conditions across, within, and between these ecoregions. Between ecoregions at the species and community level, we expected niche hypervolumes to be different and driven by regional biophysical effects on foliar N and P concentrations. At the community level, we expected niche hypervolume displacement and expansion patterns for fir and birch, respectively – patterns that reflect their resource strategy.</span></p> <p><strong><span>Results</span></strong><span>: at the species level, foliar elemental niche hypervolumes between ecoregions differed significantly for fir (F = 14.591, p-value = 0.001) and birch (F = 75.998, p-value = 0.001) with higher foliar N and P in the northern ecoregion. At the community level, across ecoregions, the foliar elemental niche hypervolume of birch differed significantly between heterospecific and conspecific groups (F = 4.075, p-value = 0.021) but not for fir. However, both species displayed niche expansion patterns, indicated by niche hypervolume increases of 35.49% for fir and 68.92% for birch. Within the northern ecoregion, heterospecific conditions elicited niche expansion responses, indicated by niche hypervolume increases for fir of 29.04% and birch of 66.48%. In the southern ecoregion we observed a contraction response for birch (niche hypervolume decreased by 3.66%), and no changes for fir niche hypervolume. Conspecific niche hypervolume comparisons between ecoregions yielded significant differences for fir and birch (F = 7.581, p-value = 0.005 and F = 8.038, p-value = 0.001) as did heterospecific comparisons (F = 6.943, p-value = 0.004, and F = 68.702, p-value = 0.001, respectively). </span></p> <p><strong><span>Conclusions</span></strong><span>: our results suggest species may exhibit biogeographical specific elemental niches – driven by biophysical differences such as those used to describe ecoregion characteristics. We also demonstrate how a species resource strategy may inform niche shift patterns in response to different community settings. Our study highlights how biogeographical differences may influence foliar elemental traits and how this may link to concepts of ecosystem and landscape functionality.</span></p>
LD matrices from the White British cohort in the UK Biobank in Zarr format
<p>This dataset contains the Linkage Disequilibrium (LD) matrices that were used in the analyses described in the manuscript:</p> <p><strong>Fast and Accurate Bayesian Polygenic Risk Modeling with Variational Inference</strong><br> Shadi Zabad, Simon Gravel, Yue Li<br> McGill University</p> <p>LD matrices record the SNP-by-SNP correlations in a given sample of individuals from a general population. In this case, we threshold the matrices so that we only record the correlations between SNPs that are at most 3 centi Morgan apart. These matrices record the SNP correlations in a random sample of 50,000 individuals from the White British cohort in the UK Biobank dataset. There is one matrix per autosomal chromosome (chr_1, chr_2, ..., chr_22). The matrices are stored in <a href="https://zarr.readthedocs.io/en/stable/">Zarr</a> format, a chunked on-disk array storage format that allows for multi-threaded read and write access.</p> <p>To access these matrices, consult the codebase of <a href="https://github.com/shz9/magenpy"><strong>magenpy</strong></a>, our custom python package with special data structures for processing these LD matrices.</p> <p>UPDATE (03/09/2022): We updated the matrices to add the reference allele attribute (A2) and we also now have one tar archive per chromosome.<br> </p>
Data belonging to the article: Estimating pre-harvest density, adult sex ratio and fecundity of white-tailed deer using wildlife cameras
<p>Adult sex ratio and fecundity (juveniles per female) are key population parameters in sustainable wildlife management, but inferring these requires abundance estimates of at least three age/sex classes of the population (male and female adults and juveniles). Prior to harvest, we used an array of 36 wildlife camera traps during 2 and 3 weeks in the early autumn of 2016 and 2017 respectively. We recorded white-tailed deer adult males, adult females and fawns from the pictures. Simultaneously, we collected fecal DNA (fDNA) from 92 20mx20m plots placed in 23 clusters of four plots between the camera traps. We identified individuals from fDNA samples with microsatellite markers and estimated the total sex ratio and population density using Spatial Capture Recapture (SCR). The fDNA-SCR analysis concluded equal sex ratio in the first year and female bias in the second year, and no difference in space use between sexes (fawns and adults combined). Camera information was analyzed in a Spatial Capture (SC) framework assuming an informative prior for animals' space use, either (1) as estimated by fDNA-SCR (same for all age/sex classes), (2) as assumed from the literature (space use of adult males larger than adult females and fawns), (3) by inferring adult male space use from individually-identified males from the camera pictures. These various SC approaches produced plausible inferences on fecundity, but also inferred total density to be lower than the estimate provided by fDNA-SCR in one of the study years. SC approaches where adult male and female were allowed to differ in their space use suggested the population had a female-biased adult sex ratio. In conclusion, SC approaches allowed estimating the pre-harvest population parameters of interest and provided conservative density estimates.</p>
Text-fig. 1. Location of the study site. a: the location of Lühe Town, Yunnan, SW China; b: fossil bearing section, white arrow indicates the fossil collection stratum; c: geological map of fossil site. in Fraxinus L. (Oleaceae) Fruits From The Early Oligocene Of Southwest China And Their Biogeographic Implications
Text-fig. 1. Location of the study site. a: the location of Lühe Town, Yunnan, SW China; b: fossil bearing section, white arrow indicates the fossil collection stratum; c: geological map of fossil site.
Text-fig. 8. SEM (a, b) and SRXTM (c, d) images of fruit associated with Miranthus elegans and Miranthus kvacekii; Mira locality, Portugal. a: Apical view of capsular fruit with five, partly open valves revealing the enclosed reticulate seeds (arrows). b: Detail of fruit wall showing an enclosed seed (arrow). c: Transverse section (orthoslice xy1200) of fruit showing central column (cc) of placenta and numerous angular and bitegmic seeds; note that the outer integument (black arrow) is thicker than inner integument (white arrow). d: Longitudinal section (orthoslice yz1239) of fruit showing perigynous attachment of calyx, central column (cc) of the placenta and sections through seeds. Specimen, Mira 99-S156331 (a–d). Scale bars = 600 µm (a, c, d), 200 µm (b). in Early Flowers Of Primuloid Ericales From The Late Cretaceous Of Portugal And Their Ecological And Phytogeographic Implications
Text-fig. 8. SEM (a, b) and SRXTM (c, d) images of fruit associated with Miranthus elegans and Miranthus kvacekii; Mira locality, Portugal. a: Apical view of capsular fruit with five, partly open valves revealing the enclosed reticulate seeds (arrows). b: Detail of fruit wall showing an enclosed seed (arrow). c: Transverse section (orthoslice xy1200) of fruit showing central column (cc) of placenta and numerous angular and bitegmic seeds; note that the outer integument (black arrow) is thicker than inner integument (white arrow). d: Longitudinal section (orthoslice yz1239) of fruit showing perigynous attachment of calyx, central column (cc) of the placenta and sections through seeds. Specimen, Mira 99-S156331 (a–d). Scale bars = 600 µm (a, c, d), 200 µm (b).
Text-fig. 11. Permian ichthyofaunas from the French Massif Central. Preliminary comparisons based on total accounts of individuals (see text for explanations). Sharks in green, Acanthodes sp. in yellow, Actinopterygians in blue, Dipnoi in white (not visible but present at Autun; see Tab. 1 for details). Each circle is proportional to the total number of specimens recovered. Permian outcrops in black. Hercynian basement indicated by vertical lines. Map modified from Gand and Durand (2006). in New Actinopterygians From The Permian Of The Brive Basin, And The Ichthyofaunas Of The French Massif Central
Text-fig. 11. Permian ichthyofaunas from the French Massif Central. Preliminary comparisons based on total accounts of individuals (see text for explanations). Sharks in green, Acanthodes sp. in yellow, Actinopterygians in blue, Dipnoi in white (not visible but present at Autun; see Tab. 1 for details). Each circle is proportional to the total number of specimens recovered. Permian outcrops in black. Hercynian basement indicated by vertical lines. Map modified from Gand and Durand (2006).
Text-fig. 19. Turritella shell from White Patch Fossil Site 1. a: stereo lateral view; b: obverse view to show the spiral ridges. in Stratigraphy, Chronology And Palaeontology Of The Tertiary Rocks Of The Cheringoma Plateau, Mozambique
Text-fig. 19. Turritella shell from White Patch Fossil Site 1. a: stereo lateral view; b: obverse view to show the spiral ridges.
Text-fig. 16. Photomicrographs of thin sections of specimen BP/16/1734, Terminalioxylon mozambicense sp. nov. from Mhengere Hill, Gorongosa, Mozambique. a: TS with round vessels, scanty paratracheal to vasicentric parenchyma, diffuse and narrow terminal or initial bands; b: TS at higher magnification, note the very narrow rays; c: TLS, vessels with small alternate pits, and partly tylosed; d–g: TLS with crystals (small white arrows) in the parenchyma cells, medium to thick-walled fibres and uniseriate, low rays; h: TLS, rays up to 20 cells high; i: RLS rays with procumbent body cells and 1–2 rows of marginal upright cells. in Stratigraphy, Chronology And Palaeontology Of The Tertiary Rocks Of The Cheringoma Plateau, Mozambique
Text-fig. 16. Photomicrographs of thin sections of specimen BP/16/1734, Terminalioxylon mozambicense sp. nov. from Mhengere Hill, Gorongosa, Mozambique. a: TS with round vessels, scanty paratracheal to vasicentric parenchyma, diffuse and narrow terminal or initial bands; b: TS at higher magnification, note the very narrow rays; c: TLS, vessels with small alternate pits, and partly tylosed; d–g: TLS with crystals (small white arrows) in the parenchyma cells, medium to thick-walled fibres and uniseriate, low rays; h: TLS, rays up to 20 cells high; i: RLS rays with procumbent body cells and 1–2 rows of marginal upright cells.
Text-fig. 21. Femur head from White Patch Bone Site belonging to a large mammal approximately the size of a pygmy hippopotamus, probably an embrithopod. View of ligamentary fossa. in Stratigraphy, Chronology And Palaeontology Of The Tertiary Rocks Of The Cheringoma Plateau, Mozambique
Text-fig. 21. Femur head from White Patch Bone Site belonging to a large mammal approximately the size of a pygmy hippopotamus, probably an embrithopod. View of ligamentary fossa.
Text-fig. 20. Proximal right ulna of an embrithopod from White Patch Bone Site. a: lateral view; b: proximal view (anterior to the left); c: stereo view of the articular surface for the humerus. Note the damaged medial and lateral sides of the articular surface (dotted lines) which makes the distal part of the articular surface look narrower than it would have been in life. in Stratigraphy, Chronology And Palaeontology Of The Tertiary Rocks Of The Cheringoma Plateau, Mozambique
Text-fig. 20. Proximal right ulna of an embrithopod from White Patch Bone Site. a: lateral view; b: proximal view (anterior to the left); c: stereo view of the articular surface for the humerus. Note the damaged medial and lateral sides of the articular surface (dotted lines) which makes the distal part of the articular surface look narrower than it would have been in life.
Text-fig. 17. White Patch fossil sites (18°56′10.9″S: 34°38′41.0″E) Gorongosa National Park, south of the 4×4 vehicle track from Urema to Muanza. 1 – Marine molluscs, 2 – Bones, 3 – Bones, 4 – Marine snails (these sites were subsequently named GPL 12 and GPL 12b by d'Oliveira Coelho et al. 2021). Image modified from Google Earth. in Stratigraphy, Chronology And Palaeontology Of The Tertiary Rocks Of The Cheringoma Plateau, Mozambique
Text-fig. 17. White Patch fossil sites (18°56′10.9″S: 34°38′41.0″E) Gorongosa National Park, south of the 4×4 vehicle track from Urema to Muanza. 1 – Marine molluscs, 2 – Bones, 3 – Bones, 4 – Marine snails (these sites were subsequently named GPL 12 and GPL 12b by d'Oliveira Coelho et al. 2021). Image modified from Google Earth.
Text-fig. 7. Geology of the Muaredzi-Muanza sector of the Cheringoma Plateau showing the location of fossil occurrences. White stars – fossiliferous localities mapped by Pickford (2012, 2013), Black stars – fossil sites mapped by Habermann et al. (2019) and d'Oliveira Coelho et al. (2021) (GPL 12 and GPL 12b correspond to the White Patch sites). TTI – Cheringoma Formation, TTs1 – Mazamba Formation, TTs1a – Palaeopan facies, TTs2 – Inhaminga Formation, Qc – Quaternary sediments. The base map is modified from Google Earth. in Stratigraphy, Chronology And Palaeontology Of The Tertiary Rocks Of The Cheringoma Plateau, Mozambique
Text-fig. 7. Geology of the Muaredzi-Muanza sector of the Cheringoma Plateau showing the location of fossil occurrences. White stars – fossiliferous localities mapped by Pickford (2012, 2013), Black stars – fossil sites mapped by Habermann et al. (2019) and d'Oliveira Coelho et al. (2021) (GPL 12 and GPL 12b correspond to the White Patch sites). TTI – Cheringoma Formation, TTs1 – Mazamba Formation, TTs1a – Palaeopan facies, TTs2 – Inhaminga Formation, Qc – Quaternary sediments. The base map is modified from Google Earth.
Text-fig. 13. a, d–g: Acer aemilianum. b, c: Acer palmatum and A. sieboldianum modern leaves (NMNS Cleared Leaf Database). a: Oriolo MSF 661, 7-lobed leaf. b: Specimen U 1049, lobe detail showing finely serrate leaf margin. c: Specimen T 0246, 9-lobed leaf with coarsely serrate leaf margin. d: Oriolo MSF 645-1, 9-lobed leaf with two small additional lobes. e: Oriolo MSF 645. f: Oriolo MSF 660, 9-lobed specimen. g: Oriolo MSF 660-1. White arrows indicate position along lamina lobes where marginal serration starts. Scale bars 10 mm (a–c, f, g), 50 mm (d, e). in The Late Early Pleistocene Flora Of Oriolo, Faenza (Italy): Assembly Of The Modern Forest Biome
Text-fig. 13. a, d–g: Acer aemilianum. b, c: Acer palmatum and A. sieboldianum modern leaves (NMNS Cleared Leaf Database). a: Oriolo MSF 661, 7-lobed leaf. b: Specimen U 1049, lobe detail showing finely serrate leaf margin. c: Specimen T 0246, 9-lobed leaf with coarsely serrate leaf margin. d: Oriolo MSF 645-1, 9-lobed leaf with two small additional lobes. e: Oriolo MSF 645. f: Oriolo MSF 660, 9-lobed specimen. g: Oriolo MSF 660-1. White arrows indicate position along lamina lobes where marginal serration starts. Scale bars 10 mm (a–c, f, g), 50 mm (d, e).
Text-fig. 4. Type specimens of Magnolia allasoniae MARTINETTO sp. nov. from the Pliocene locality Ca' Viettone. a1–a4: Holotype (MGPT-PU141081) in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 5) in a black and white print (a1), in a new digital photograph in basal view (a2), ventral view (a3) and dorsal view (a4); b1–b4: Paratype MGPT-PU141082 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 4) in a black and white print (b1), in a new digital photograph in basal view (b2), ventral view (b3) and dorsal view (b4); c1–c4: Paratype MGPT-PU141083 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 6) in a black and white print (c1), in a new digital photograph in basal view (c2), ventral view (c3) and dorsal view (c4); d1–d4: Paratype MGPT-PU141084 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 7) in a black and white print (d1), in a new digital photograph in basal view (d2), ventral view (d3) and internal view (d4). Scale bars 1 mm. in Late Messinian Flora From The Post-Evaporitic Deposits Of The Piedmont Basin (Northwest Italy)
Text-fig. 4. Type specimens of Magnolia allasoniae MARTINETTO sp. nov. from the Pliocene locality Ca' Viettone. a1–a4: Holotype (MGPT-PU141081) in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 5) in a black and white print (a1), in a new digital photograph in basal view (a2), ventral view (a3) and dorsal view (a4); b1–b4: Paratype MGPT-PU141082 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 4) in a black and white print (b1), in a new digital photograph in basal view (b2), ventral view (b3) and dorsal view (b4); c1–c4: Paratype MGPT-PU141083 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 6) in a black and white print (c1), in a new digital photograph in basal view (c2), ventral view (c3) and dorsal view (c4); d1–d4: Paratype MGPT-PU141084 in different views, i.e., as originally figured in Martinetto (1995: pl. 1, fig. 7) in a black and white print (d1), in a new digital photograph in basal view (d2), ventral view (d3) and internal view (d4). Scale bars 1 mm.
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.