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Distribution. Restricted and patchy range in NE Madagascar that includes the humid forest belt extending from the Marojejy Massif and the Andapa Basin to Maroantsetra; the Androranga River may be the NE distributional limit in the Tsaratanana Corridor, although further surveys are needed to confirm this, and the Antainambalana River in the Makira Forest protected area is currently regarded as the S boundary. Currently, Marojejy represents the N limit ofits distribution, although historic range maps suggest that it once occurred as far N as the Bemarivo River near Sambava. The NE distributional limit in Makira was only recently established, when a few groups were found in the Antohaka Lava Forest, but informal reports suggest that the unprotected Maherivaratra Forest, outside NE Makira, may also contain Silky Sifakas. in Indriidae
Distribution. Restricted and patchy range in NE Madagascar that includes the humid forest belt extending from the Marojejy Massif and the Andapa Basin to Maroantsetra; the Androranga River may be the NE distributional limit in the Tsaratanana Corridor, although further surveys are needed to confirm this, and the Antainambalana River in the Makira Forest protected area is currently regarded as the S boundary. Currently, Marojejy represents the N limit ofits distribution, although historic range maps suggest that it once occurred as far N as the Bemarivo River near Sambava. The NE distributional limit in Makira was only recently established, when a few groups were found in the Antohaka Lava Forest, but informal reports suggest that the unprotected Maherivaratra Forest, outside NE Makira, may also contain Silky Sifakas.
Hyperspectral Multipoint High-Speed Confocal Microscopy Supporting Information Movies
<p><strong>S1 Movie. Neuronal growth in a zebrafish embryo</strong>. Sensory neurons (green) are labeled with GFP and motor neurons (magenta) are labelled with mCherry. The video was captured with filter configuration 2 (see section "System Dichroics and Emission Filters") frames were taken every minute.</p> <p> </p><p><strong>S2 Movie. Video of mitosis in a live <em>Xenopus laevis</em> embryo.</strong> The cellular membranes (magenta) is labelled with mTagBFP::CAAX; chromatin (blue) is labelled with miRFP670::H2B; and mitotic spindles (green) are labelled with mCherry:α-tubulin. One frame of 75 ms exposure time was captured every 5 seconds. The video was captured with filter configuration 2 (see section "System Dichroics and Emission Filters").</p> <p></p>
Enhancing georeferenced biodiversity inventories: automated information extraction from literature records reveal the gaps
<p>Data and code supplement to our article revised submission to PeerJ.</p> <p> </p> <p>The file is compressed using standard zip. The uncompressed size is about 50 GB. There is a readme.md in the archive, which explains the structure of the contents.</p> <p> </p> <p>Abstract:</p> <p>We use natural language processing (NLP) to retrieve location data for cheilostome bryozoan species (text-mined occurrences [TMO]) in an automated procedure. We compare these results with data combined from two major public databases (DB): the Ocean Biogeographic Information System (OBIS), and the Global Biodiversity Information Facility (GBIF). Using DB and TMO data separately and in combination, we present latitudinal species richness curves using standard estimators (Chao2 and the Jackknife) and range-through approaches. Our combined DB and TMO species richness curves quantitatively document a bimodal global latitudinal diversity gradient for extant cheilostomes for the first time, with peaks in the temperate zones. 79% of the georeferenced species we retrieved from TMO (N = 1408) and DB (N = 4549) are non-overlapping. Despite clear indications that global location data compiled for cheilostomes should be improved with concerted effort, our study supports the view that many marine latitudinal species richness patterns deviate from the canonical latitudinal diversity gradient (LDG). Moreover, combining online biodiversity databases with automated information retrieval from the published literature is a promising avenue for expanding taxon-location datasets.</p>
ARCHI4MOM: Using Tracing Information to Extract the Architecture of Microservice-based Systems from Message-oriented Middleware
<p>The data published here are relevant for ESCA_2022 publication. </p>
Supporting Information: Assessing the Social Dimension in Strategic Network Design for a Sustainable Development: The Case of Bioethanol Production in the EU
<p>Supporting Information S2 provides all parameters of the optimization model, both those associated with the social objective and hotspot functions of the study at hand, and those from the underlying model by Wietschel et al. (2021). To put the method of the study into perspective, it also gives an overview of referenced frameworks (GSLCAPO, SHDB, SDGs) and their categories, subcategories, and indicators. Furthermore, it includes detailed results for all social, environmental, and economic objective functions in all scenarios, and of the Pareto optimization. Lastly, the underlying data for all figures of the manuscript and Supporting Information S1 is provided.</p>
FIGURE 5. Chusquea spetentrionalis. A–C in A new informal group in Chusquea subg. Swallenochloa (Poaceae: Bambusoideae: Bambuseae) and emended descriptions for the Mexican endemics C. enigmatica and C. septentrionalis
FIGURE 5. Chusquea spetentrionalis. A–C. Flowering clumps from Durango (A, C) and Sinaloa (B). D. Flowering branches showing synflorescences. E. Synflorescence showing spikelets. Photos by Arturo Castro-Castro.
FIGURE 2 in A new informal group in Chusquea subg. Swallenochloa (Poaceae: Bambusoideae: Bambuseae) and emended descriptions for the Mexican endemics C. enigmatica and C. septentrionalis
FIGURE 2. Geographical distribution map of Chusquea enigmatica and C. septentrionalis. Black squares belong to C. enigmatica, black triangles are localities of C. septentrionalis. Black arrows indicate the type locality for each species. Dotted line indicates previous northernmost Chusquea collections.
FIGURE 3. Chusquea enigmatica. A in A new informal group in Chusquea subg. Swallenochloa (Poaceae: Bambusoideae: Bambuseae) and emended descriptions for the Mexican endemics C. enigmatica and C. septentrionalis
FIGURE 3. Chusquea enigmatica. A. Plants of C. enigmatica in the understory of the montane cloud forest in the State of San Luis Potosí, Mexico. B. Plants of C. enigmatica growing in a clearing of the montane cloud forest in the State of Hidalgo, Mexico. C. Leptmorph rhizome. D-E. Branches and foliage leaves from Hidalgo (D) and San Luis Potosí (E). A, E. Photos by Julián Hernández Rendón. B-D. Photos by Eduardo Ruiz-Sanchez.
FIGURE 1. Chusquea enigmatica. A. Synflorescence. B. Spikelet. C in A new informal group in Chusquea subg. Swallenochloa (Poaceae: Bambusoideae: Bambuseae) and emended descriptions for the Mexican endemics C. enigmatica and C. septentrionalis
FIGURE 1. Chusquea enigmatica. A. Synflorescence. B. Spikelet. C. Lower glumes (I, II). D. Upper glumes (III, IV). E. Lemma (left) and palea (right). Based on S. Zamudio, J. Ceja & A. Mendoza 17454. Illustration by Juvenal Aragón Parada.
Additional Supporting Information to 'Quantifying the Contribution of Ocean Mesoscale Eddies to Low Oxygen Extreme Events.'
<p>Additional Supporting Information to 'Quantifying the Contribution of Ocean Mesoscale Eddies to Low Oxygen Extreme Events.'. Submitted to Geophysical Research Letters for publication. 2022.</p> <p>NetCDF files and Python NumPy arrays of data used to create all figures in the manuscript main text and supporting information.</p>
Natural history predicts patterns of thermal vulnerability in amphibians from the Atlantic rainforest of Brazil_supporting information
<p>In the Brazilian Atlantic Rainforest (AF), amphibians (625 species) face habitat degradation leading to stressful thermal conditions that constrain animal activity (e.g. foraging, reproduction). Data on thermal ecology for these species is still scarce. We tested the hypothesis that environmental occupation affects the thermal tolerance of amphibian species more than their phylogenetic relationships. We evaluated patterns of thermal tolerance of 47 amphibian species by assessing critical thermal maxima and warming tolerances, relating these variables with ecological covariates (e.g. adult macro- and microhabitat and site of larval development). We used mean and maximum environmental temperature, ecological covariates, and morphological measurements in the phylogenetic generalized least squares models selection to evaluate which traits better predict thermal tolerance. We did not recover phylogenetic signal under a Brownian model; our results point to a strong association between critical thermal maxima and habitat and development site. Forest species were less tolerant to warm temperatures than open area or generalist species. Species with larvae that develop in lentic environment were more tolerant than those from lotic ones. Thus, species inhabiting forest microclimates are more vulnerable to the synergistic effect of habitat loss and climatic change. We use radar charts as a quick evaluation tool for thermal risk diagnoses using aspects of natural history as axes.</p>
Quantifying mothers' preferences for providing information about non-invasive prenatal testing in Sweden: evidence from a discrete choice experiment
<p>Training materials for a discrete choice experiment survey designed to quantify mothers' preferences for information about non-invasive prenatal testing in Sweden.</p>
Survey and case studies information in South Asia
<p>Supplementary information from South Asia component of the CLACSO IDRC Research Assessment Project. </p>
Nesokia is sister to Bandicota and are nested in Rattus phylogenetically, making Rat- tus paraphyletic. Tarsomys, Limnomys, and Diplothrix are also phylogenetically in Rat- tus, and the clade is in need of focused re- vision at the generic level. Nesokia bunnui was originally described as a separate ge-nus, Erythronesokia, because it is morphologically very distinctive from N. indica. Type specimen was destroyed during the Iraq War, and a neotype was recently designated to replace it. Monotypic. Distribution. Tigris and Euphrates river valleys, SE Iraq. Descriptive notes. Head—body 230-260 mm, tail 205-270 mm, ear 18-21 mm, hindfoot 49-58 mm; weight 519 g. The Long-tailed Bandicoot Rat is larger than the Short-tailed Bandicoot Rat (N. indica). Pelage is soft and woolly, interspersed with harsher coarse hair and long black hairs near mid-back. Dorsum is fawn to ocherous red, washed with purple or chestnuton darker individuals. Hairs are basally slate-gray and distally rufous, occasionally with whitish or black tips. Muzzle is drab. Sides arefawn, with gray edge toward venter. Venteris whitish, extending onto cheeks where the same pattern from gray to fawn to dorsal pelage occurs. Feet are large and robust, being light brown and well-furred dorsally. Claws are amber on forefeet and dull brown on hindfeet; pollux is extremely small. Ears are moderately long and brownish, with no hair internally. Tail is ¢.82-104% of head-body length and deep brownish drab, interspersed with visible white hair. Skull is large and robust, similarly to the Short-tailed Bandicoot Rat. Habitat. Marsh and swamp land. Food and Feeding. No information. Breeding. No information. Activity patterns. The Long-tailed Bandicoot Rat is terrestrial, although it isfound in swampy and marshy areas and is probably amphibious. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Longtailed Bandicoot Rat is apparently rare and is known from very few specimens. Marsh and swamp habitats in which it is found were completely destroyed during the Iraq War by draining, war damage, and agricultural expansion. In recent years, flooding from Tigris and Euphrates rivers and high snow fall and melt haveresulted in partial restoration ofits native habitat, although restoration is not a complete. Populations are now probably highly fragmented. Bibliography. Al-Ansari et al. (2012), Al-Robaae & Felten (1990), Khajuria (1981), Krystufek et al. (2017), Musser & Carleton (2005), Richardson & Hussain (2006), Stuart (2008). in Muridae
Nesokia is sister to Bandicota and are nested in Rattus phylogenetically, making Rat- tus paraphyletic. Tarsomys, Limnomys, and Diplothrix are also phylogenetically in Rat- tus, and the clade is in need of focused re- vision at the generic level. Nesokia bunnui was originally described as a separate ge-nus, Erythronesokia, because it is morphologically very distinctive from N. indica. Type specimen was destroyed during the Iraq War, and a neotype was recently designated to replace it. Monotypic. Distribution. Tigris and Euphrates river valleys, SE Iraq. Descriptive notes. Head—body 230-260 mm, tail 205-270 mm, ear 18-21 mm, hindfoot 49-58 mm; weight 519 g. The Long-tailed Bandicoot Rat is larger than the Short-tailed Bandicoot Rat (N. indica). Pelage is soft and woolly, interspersed with harsher coarse hair and long black hairs near mid-back. Dorsum is fawn to ocherous red, washed with purple or chestnuton darker individuals. Hairs are basally slate-gray and distally rufous, occasionally with whitish or black tips. Muzzle is drab. Sides arefawn, with gray edge toward venter. Venteris whitish, extending onto cheeks where the same pattern from gray to fawn to dorsal pelage occurs. Feet are large and robust, being light brown and well-furred dorsally. Claws are amber on forefeet and dull brown on hindfeet; pollux is extremely small. Ears are moderately long and brownish, with no hair internally. Tail is ¢.82-104% of head-body length and deep brownish drab, interspersed with visible white hair. Skull is large and robust, similarly to the Short-tailed Bandicoot Rat. Habitat. Marsh and swamp land. Food and Feeding. No information. Breeding. No information. Activity patterns. The Long-tailed Bandicoot Rat is terrestrial, although it isfound in swampy and marshy areas and is probably amphibious. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Longtailed Bandicoot Rat is apparently rare and is known from very few specimens. Marsh and swamp habitats in which it is found were completely destroyed during the Iraq War by draining, war damage, and agricultural expansion. In recent years, flooding from Tigris and Euphrates rivers and high snow fall and melt haveresulted in partial restoration ofits native habitat, although restoration is not a complete. Populations are now probably highly fragmented. Bibliography. Al-Ansari et al. (2012), Al-Robaae & Felten (1990), Khajuria (1981), Krystufek et al. (2017), Musser & Carleton (2005), Richardson & Hussain (2006), Stuart (2008).
Distribution. Mt Cameroon, W Cameroon, and Bioko I, Equatorial Guinea. Descriptive notes. Head-body 100- 130 mm, tail 110-147 mm, ear 16-20 mm, hindfoot 21-25 mm; weight 27-62 g. Fur of the Cameroon Soft-furred Mouse is dark rufous-brown to blackish brown above and pale to dark gray below. Tail is very long (c.112% of head-body length) and dark. Hindfeet and forefeet are dark brown. Females have three pairs of nipples. Habitat. Montane forest and alpine grassland at elevations above 1000 m. Food and Feeding. No information. Breeding. Gestation lasts 26-30 days. Litters have 2-6 young. Activity patterns. The Cameroon Soft-furred Mouse is nocturnal and terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Cameroon Soft-furred Mouse occurs in two disjunct areas occupying only ¢.2900 km? and the extent and quality of its forest habitat continue to decline. Bibliography. Eisentraut (1970, 1973), Happold (2013a), Missoup et al. (2012), Monadjem etal. (2015). in Muridae
Distribution. Mt Cameroon, W Cameroon, and Bioko I, Equatorial Guinea. Descriptive notes. Head-body 100- 130 mm, tail 110-147 mm, ear 16-20 mm, hindfoot 21-25 mm; weight 27-62 g. Fur of the Cameroon Soft-furred Mouse is dark rufous-brown to blackish brown above and pale to dark gray below. Tail is very long (c.112% of head-body length) and dark. Hindfeet and forefeet are dark brown. Females have three pairs of nipples. Habitat. Montane forest and alpine grassland at elevations above 1000 m. Food and Feeding. No information. Breeding. Gestation lasts 26-30 days. Litters have 2-6 young. Activity patterns. The Cameroon Soft-furred Mouse is nocturnal and terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List. The Cameroon Soft-furred Mouse occurs in two disjunct areas occupying only ¢.2900 km? and the extent and quality of its forest habitat continue to decline. Bibliography. Eisentraut (1970, 1973), Happold (2013a), Missoup et al. (2012), Monadjem etal. (2015).
The first comprehensive revision of all the species attributed to Melomys led J. I. Menzies in 1996 to resurrect the genus Paramelomys and to redefine its morphologicallimits and species content. Menzies created P. gressitti as a new species belonging to a group displaying morphological similarities and including also P. lorentzii and P. moncktoni. Monotypic Distribution. E New Guinea. Descriptive notes. Head-body 135-162 mm, hindfoot 30-34 mm; no specific data are available for body weight. Gressitt's Mosaic-tailed Rat is a medium-sized Paramelomys with a soft, thick and woolly pelage, a long narrow foot, and a tail with three hairs per scale. It exhibits a medium-sepia dorsal pelage and a gray-buff ventral one. Tail is slightly shorter (99%) than head-body length. The skull has a narrow zygomatic plate. Habitat. Moist tropical mountain forest between 2300 m and 2400 m. Food and Feeding. No information. Breeding. No information. Activity patterns. Gressitt's Mosaic-tailed Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List owing to its small geographic range (less than 3500 km?*) and the destruction ofits habitat by mining and logging activities. The major threat to Gressitt's Mosaic-tailed Rat is ongoing habitat degradation caused by nearby human populations; habitat on Mount Kandy has been destroyed by gold-miners and wood-cutters. Bibliography. Menzies (1996). in Muridae
The first comprehensive revision of all the species attributed to Melomys led J. I. Menzies in 1996 to resurrect the genus Paramelomys and to redefine its morphologicallimits and species content. Menzies created P. gressitti as a new species belonging to a group displaying morphological similarities and including also P. lorentzii and P. moncktoni. Monotypic Distribution. E New Guinea. Descriptive notes. Head-body 135-162 mm, hindfoot 30-34 mm; no specific data are available for body weight. Gressitt's Mosaic-tailed Rat is a medium-sized Paramelomys with a soft, thick and woolly pelage, a long narrow foot, and a tail with three hairs per scale. It exhibits a medium-sepia dorsal pelage and a gray-buff ventral one. Tail is slightly shorter (99%) than head-body length. The skull has a narrow zygomatic plate. Habitat. Moist tropical mountain forest between 2300 m and 2400 m. Food and Feeding. No information. Breeding. No information. Activity patterns. Gressitt's Mosaic-tailed Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List owing to its small geographic range (less than 3500 km?*) and the destruction ofits habitat by mining and logging activities. The major threat to Gressitt's Mosaic-tailed Rat is ongoing habitat degradation caused by nearby human populations; habitat on Mount Kandy has been destroyed by gold-miners and wood-cutters. Bibliography. Menzies (1996).
Lophuromys stanley: is member of the L. flavopunctatus species complex and was named during partial revision of the L. aguilus species complex. It is characterized by craniometric and genetic character-istics; its skull proportions are similar to L. laticeps, and molecularly, it is similar to L. margarettae and L. zena (cytochrome-b). Lophuromys stanleyi is one of four endemic species in the Rwenzori Mountains diversity hotspot. Monotypic. Distribution. Rwenzori Mts, E DR Congo and SW Uganda. Descriptive notes. Head-body 113-126 mm, tail 40-80 mm, ear 16-19 mm, hindfoot 22-24 mm; weight 36-55 g. The Rwenzori Brush-furred Rat has a speckled pelage similar to other speciesin the L. flavopunctatus species complex. Tail is short, 50-60% of head-body length. Habitat. Poorly known, but type specimen was collected at an elevation of 3700 m. Food and Feeding. No information. Breeding. No information. Activity patterns. No information. in Muridae
Lophuromys stanley: is member of the L. flavopunctatus species complex and was named during partial revision of the L. aguilus species complex. It is characterized by craniometric and genetic character-istics; its skull proportions are similar to L. laticeps, and molecularly, it is similar to L. margarettae and L. zena (cytochrome-b). Lophuromys stanleyi is one of four endemic species in the Rwenzori Mountains diversity hotspot. Monotypic. Distribution. Rwenzori Mts, E DR Congo and SW Uganda. Descriptive notes. Head-body 113-126 mm, tail 40-80 mm, ear 16-19 mm, hindfoot 22-24 mm; weight 36-55 g. The Rwenzori Brush-furred Rat has a speckled pelage similar to other speciesin the L. flavopunctatus species complex. Tail is short, 50-60% of head-body length. Habitat. Poorly known, but type specimen was collected at an elevation of 3700 m. Food and Feeding. No information. Breeding. No information. Activity patterns. No information.
Lophuromys medicaudatus, L. woosnami, and L. luteogaster are in subgenus Kivumys and woosnami species group. Monotypic. Distribution. Endemic to the Albertine Rift, occurring around Lake Kivu in E DR Congo and Rwanda and SW Uganda (Bwindi). Descriptive notes. Head—body 92-112 mm, tail 73-95 mm, ear 15-19 mm, hindfoot 18-23 mm; weight 29-43 g. Similar to other species in subgenus Kivumys, the Western Rift Brush-furred Rat has unspeckled pelage, and tail ¢.85% of head-body length. Dorsum is uniform dark brown-olive, and venter is orange. Females have three pairs of mammae. Habitat. Mountain swamps and mountain forests at elevations of 1850-2500 m. Food and Feeding. The Western Rift Brush-furred Rat is omnivorous; diets contain 30-100% arthropods, mollusks, seeds, and fruits. Breeding. Female Western Rift Brush-furred Rats can have 1-2 embryos. Pregnant females were observed in February, April, and July. Activity patterns. The Western Rift Brush-furred Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Vulnerable on The IUCN Red List. The Western Rift Brush-furred Rat has never been found in modified secondary environment and is quite rare. Bibliography. Dieterlen (1976b, 1987 2013g), Kasangaki et al. (2003), Verheyen et al. (1996). in Muridae
Lophuromys medicaudatus, L. woosnami, and L. luteogaster are in subgenus Kivumys and woosnami species group. Monotypic. Distribution. Endemic to the Albertine Rift, occurring around Lake Kivu in E DR Congo and Rwanda and SW Uganda (Bwindi). Descriptive notes. Head—body 92-112 mm, tail 73-95 mm, ear 15-19 mm, hindfoot 18-23 mm; weight 29-43 g. Similar to other species in subgenus Kivumys, the Western Rift Brush-furred Rat has unspeckled pelage, and tail ¢.85% of head-body length. Dorsum is uniform dark brown-olive, and venter is orange. Females have three pairs of mammae. Habitat. Mountain swamps and mountain forests at elevations of 1850-2500 m. Food and Feeding. The Western Rift Brush-furred Rat is omnivorous; diets contain 30-100% arthropods, mollusks, seeds, and fruits. Breeding. Female Western Rift Brush-furred Rats can have 1-2 embryos. Pregnant females were observed in February, April, and July. Activity patterns. The Western Rift Brush-furred Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Vulnerable on The IUCN Red List. The Western Rift Brush-furred Rat has never been found in modified secondary environment and is quite rare. Bibliography. Dieterlen (1976b, 1987 2013g), Kasangaki et al. (2003), Verheyen et al. (1996).
Supplementary Information - Circulating insulin-like growth factor system adaptations in hibernating brown bears indicate increased tissue IGF availability
<p>Supplementary figures and tables for the manuscript entitled “Circulating insulin-like growth factor system adaptations in hibernating brown bears indicate increased tissue IGF availability”.</p>
Information of indentified metabolites in metabolomic analysis and summary of the major mass-spectrometry-based studies performed on the syphilis patients or neurosyphilis patients to date
<p>Supplementary Table S1. Information of indentified metabolites in metabolomic analysis. <br> Supplementary Table S2. Summary of the major mass-spectrometry-based studies performed on the syphilis patients or neurosyphilis patients to date. Table includes details about the numbers of sample, the analysis method, and the type of mass spectrometer used and biomarkers identified in previous study.eng</p>
ScienceDex guides
Understand access before you commit
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.