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984 results for “migratory”
Fig. 1 in Prevalence and genetic diversity of haematozoa in South American waterfowl and evidence for intercontinental redistribution of parasites by migratory birds
Fig. 1. Map of sampling locations in Peru and Argentina. The number of waterfowl blood samples collected at each site is provided in parentheses.
F I G U R E 6 in Three-dimensional migratory behaviour of European silver eels (Anguilla anguilla) approaching a hydropower plant
F I G U R E 6 Correlation between relative swimming depths and inflow discharge for upstream- and downstream-swimming eels during the day and night in the river reach. Solid lines represent significant relationships, broken lines insignificant ones. Situation:, downstream day;, downstream night;, upstream day;, upstream night
Historical baleen plates indicate that once abundant Antarctic blue and fin whales demonstrated distinct migratory and foraging strategies
<p>Southern hemisphere blue (<em>Balaenoptera musculus intermedia</em>) and fin (<em>Balaenoptera physalus</em>) whales are the largest predators in the Southern Ocean, with similarities in morphology and distribution. Yet, understanding of their life history and foraging is limited due to current low abundances and limited ecological data. To address these gaps, historic Antarctic blue (n = 5) and fin (n = 5) whale baleen plates, collected in 1947–1948 and recently rediscovered in the Smithsonian National Museum of Natural History, were analyzed for bulk (δ<sup>13</sup>C and δ<sup>15</sup>N) stable isotopes. Regular oscillations in isotopic ratios, interpreted as annual cycles, revealed that baleen plates contain approximately six years (14.35 ± 1.20 cm yr<sup>–1</sup>) of life history data in blue whales and four years (16.52 ± 1.86 cm yr<sup>–1</sup>) in fin whales. Isotopic results suggest that: 1) in the 1940s, blue and fin whales fed at the same trophic level but in slightly different habitats, 2) fin whales appear to have had more regular annual migrations, and 3) fin whales may have migrated to ecologically distinct sub-Antarctic waters annually while some blue whales may have resided year-round in the Southern Ocean. These results reveal differences in ecological niche and life history strategies between Antarctic blue and fin whales during a period when their populations were more abundant than today, and before major human-driven climatic changes occurred in the Southern Ocean.</p>
Incidents of death and missing people on migratory routes around the world
<pre>Dataset with data on incidents of people dead or missing on international migratory routes in different regions, from the website https://missingmigrants.iom.int/, from the Missing Migrants Project of the International Organisation for Migration (IOM). </pre>
Data from: Environmental drivers of population-level variation in the migratory and diving ontogeny of an Arctic top predator
<p>The development of migratory strategies that enable juveniles to survive to recruitment is critical for species that exploit seasonal niches. For animals that forage via breath-hold diving this requires a combination of both physiological and foraging skill development. Here, we assess how migratory and dive behaviour develop over the first months of life for a migratory Arctic top predator, the harp seal, tracked using animal-borne satellite relay data loggers. We reveal similarities in migratory movements and differences in diving behaviour between juveniles from breeding populations in the Northwest Atlantic and Greenland Sea. In both regions, periods of resident and transient behaviour during migration were associated with proxies for food availability; sea ice concentration and water depth. However, while ontogenetic development of dive behaviour was similar for both groups of juveniles over the first 25 days, after this time Greenland Sea animals performed shorter and shallower dives and were more closely associated with sea ice than Northwest Atlantic animals. Together, these results highlight the role of both intrinsic and extrinsic factors in shaping early-life behaviour. Differences in the environmental conditions experienced during early-life may shape how populations respond to the rapid changes occurring in the Arctic ocean ecosystem.</p>
Data from: Integrating tracking and resight data enables unbiased inferences about migratory connectivity and winter range survival from archival tags
<p>Archival geolocators have transformed the study of small, migratory organisms but analysis of data from these devices requires bias correction because tags are only recovered from individuals that survive and are re-captured at their tagging location. Data and code provided in this repository can be used to replicate the simulation and Painted Bunting case study results presented by Rushing et al. (2021) showing that integrating geolocator recovery data and mark–resight data enables unbiased estimates of both migratory connectivity between breeding and nonbreeding populations and region-specific survival probabilities for wintering locations.</p>
BirdVox-full-season: 6672 hours of audio from migratory birds
<p><strong>BirdVox-full-season: 6672 hours of audio from migratory birds</strong></p> <p><strong>================================================</strong></p> <p>Version 1.1, May 2022.</p> <p> </p> <p>The full-season dataset contains 6671 hours of audio from the Fall 2015 migration season in Tompkins County, NY.</p> <p> </p> <p><strong>Created By</strong></p> <p><strong>---------------</strong></p> <p>Andrew Farnsworth (1), Benjamin Mark Van Doren (1), Steve Kelling (1), Vincent Lostanlen (2), Justin Salamon (3), Aurora Cramer (4), Juan Pablo Bello (4)</p> <p>(1): Cornell Lab of Ornithology (CLO)</p> <p>(2): Laboratoire des Sciences du Numérique de Nantes (LS2N), CNRS</p> <p>(3): Adobe Research</p> <p>(4): New York University</p> <p>https://wp.nyu.edu/birdvox</p> <p> </p> <p><strong>Data acquisition</strong></p> <p><strong>--------------------</strong></p> <p>In 2015, we placed nine bioacoustic sensors - Recording and Observing Bird Identification Node (ROBIN) developed by the Cornell Lab of Ornithology - in residential areas of Tompkins County, NY, USA, primarily surrounding the town of Ithaca, NY, USA. All sensors had the same hardware configurationcomprising a Knowles EK23132 microphone element, an analog-to-digital converter, a Raspberry Pi Model B single-board computer, a solid-state memory card, and a battery. The microphone element is omnidirectional and has an approximately flat sensitivity of 53±5 dB between 2 and 10 kHz; that is, the frequency range of flight calls. The microphone element sits at the bottom of a small horn-shaped enclosure oriented upwards. In turn, this enclosure sits inside a hard plastic housing, whose purpose is to reject lateral sound sources, such as insects or car engines.</p> <p>The analog-to-digital converter encodes the monophonic signal recorded by the microphone into a linear pulse-code modulation sequence at a sample rate of 24 kHz and a sample depth of 16 bits. This sample rate corresponds to an appropriate Nyquist bound to capture the diversity of avian flight calls, which occur almost exculsively below 11 kHz in frequency. The single-board computer streams this sequence under the form of 20-second buffers, which are progressively appended to a lossless audio file in FLAC format. This acquisition procedure is repeated every night from civil twilight dawn to dusk between August 3rd, 2015 and December 8th, 2015. This temporal period corresponds to the general pattern of the timing of nocturnal bird migration, which birds usually initiate 30-45 minutes after local sunset and cease in the hours around dawn; this is not always the case for cessation.</p> <p>This duty cycle corresponds to roughly 1,500 hours of audio per sensor, and thus 13,500 hours for the entire sensor network. However, due to intermittent failures of sensing hardware, a common feature of many autonomous recording platforms, we retrieved only 6,651 hours successfully.</p> <p>We gathered FLAC files according to their location of provenance or "unit". Note that unit09 was never deployed: hence, the unit IDs are 01, 02, 03, 04, 05, 06, 07, 08, and 10.</p> <p>Despite hard plastic housing and deployment locations that attempted to physically facilitate avoidance of non-target signal capture, these sensors captured audio of nocturally migrating birds as well as additional features of this soundscape including human activities (anthrophony), meteorological phenomena (e.g. geophony) and non-targeted avian and other biological signals (biophony). These latter signals include non-human mammals (e.g. White-tailed Deer, flying squirrel, canines), diurnal vocalizations of resident and migrant birds that are not flight calls (e.g. Blue Jays, American Crow, American Goldfinch), anurans (e.g. spring peepers), and many insect species (e.g. Fork-tailed Bush-Katydid, Snowy Tree Cricket). </p> <p> </p> <p><strong>Derivative Datasets</strong></p> <p><strong>----------------------------</strong></p> <p>A representative subset of these audio recordings were selected for annotation. Ornithologist Andrew Farnsworth used the Raven software to pinpoint and label every avian flight call in time and frequency. He found 26138 sound events, of which 21546 are flight calls from Passeriformes. Of those, 13385 are identifiable in terms of family, and 8669 are identifiable in terms of both family and species. The annotation process took over 600 hours. This subset of recordings and the corresponding annotations have been released as BirdVox-296h (<a href="https://doi.org/10.5281/zenodo.4415480">https://doi.org/10.5281/zenodo.4415480</a>). The isolated flight calls and annotations have been released as BirdVox-14SD (<a href="https://doi.org/10.5281/zenodo.3667093">https://doi.org/10.5281/zenodo.3667093</a>) and its follow-up release BirdVox-25SD (<a href="https://doi.org/10.5281/zenodo.5889214">https://doi.org/10.5281/zenodo.5889214</a>).</p> <p> </p> <p><strong>Feedback</strong></p> <p><strong>-------------</strong></p> <p>Please help us improve BirdVox-full-night by sending your feedback to:</p> <p>vincent.lostanlen@ls2n.fr and af27@cornell.edu</p> <p>In case of a problem, please include as many details as possible.</p> <p> </p> <p><strong>Acknowledgement</strong></p> <p><strong>--------------------------</strong></p> <p>We thank the following people for their contributions to the development, construction, maintenance, deployment, and acquisition of the ROBIN units: Jessie Barry, Ian Davies, Tom Fredericks, Jeff Gerbracht, Sara Keen, Holger Klinck, Anne Klingensmith, Ray Mack, Peter Marchetto, Ed Moore, Matt Robbins, Ken Rosenberg, and Chris Tessaglia-Hymes, Chris Wood. Initial data collection activities were supported by NSF 1125098, Wolf Creek Foundation, and Leon Levy Foundation; analyses were supported largely by NSF 1633206 as well as Leon Levy Foundation and NSF 1661329.</p> <p>Cornell University is located on the traditional homelands of the Gayogo̱hó꞉nǫ' (Guy-yo-KO-no) (the Cayuga Nation). The Gayogo̱hó꞉nǫ' are members of the Haudenosaunee (Ho-di-no-so-ni) Confederacy, an alliance of six sovereign Nations with a historic and contemporary presence on this land. The Confederacy precedes the establishment of Cornell University, New York state, and the United States of America. We acknowledge the painful history of Gayogo̱hó꞉nǫ' dispossession, and honor the ongoing connection of Gayogo̱hó꞉nǫ' people, past and present, to these lands and waters. We acknowledge that the land on which the data was collected is the unceded territory of the Cayuga nation.</p> <p> </p>
Data from: Evaluating staging habitat quality to advance the conservation of a declining migratory shorebird, Red Knot Calidris canutus
<p>Identifying where and when population "bottlenecks" occur is critical to the conservation of migratory species, many of which are declining precipitously worldwide. Especially challenging is the evaluation of changes to staging sites. These sites are indispensable links in the migratory cycle but are typically used only briefly.</p> <p>We devised a field-based approach to assess the quality and carrying capacity of a critical staging site in Nanpu, China, for the declining, migratory Red Knot (Calidris canutus rogersi & C. c. piersmai) during northward migration. The Nanpu tidal flat supports 50,000-100,000 Red Knots annually, and while there, the knots feed almost exclusively on the bivalve Potamocorbula laevis. We simultaneously monitored changes in the abundance of Red Knots and bivalves across the entire staging site in spring 2018.</p> <p>After taking into account potential competition with other shorebird species, we estimated that the Nanpu tidal flat was capable of supporting approximately 1.46-1.70 times the current observed level of usage of the site by Red Knots, and therefore is operating below, but close, to carrying capacity with respect to food resources for Red Knots. This result suggests that any further development of this site could harm the EAAF Red Knot population.</p> <p>Synthesis and applications: Quantitative monitoring and evaluation of habitat quality of staging sites are essential to successfully conserve declining migratory species. In particular, researchers and conservation practitioners should incorporate both population size and staging duration in order to more accurately assess the importance of different sites and to quantify how changes in staging habitat quality may translate into changes in migrant population sizes at both local and global scales.</p>
Quantifying phenology and migratory behaviours of hummingbirds using single-site dynamics and mark-detection analyses
<p>Nuanced understanding of seasonal movements of partially migratory birds is paramount to species and habitat conservation. Using nascent statistical methods, we identified migratory strategies of birds outfitted with radio-frequency identification (RFID) tags detected at RFID feeders in two sites in California, USA. We quantified proportions of migrants and residents and the seasonal phenology for each movement strategy in Allen's and Anna's hummingbirds; we also validated our methodology by fitting our model to obligate migratory black-chinned hummingbirds. Allen's and Anna's hummingbirds exhibited characteristics of facultative migratory behaviour. We also quantified apparent annual survival for each migratory strategy and found that residents had significantly higher probabilities of apparent survival. Low survival estimates for migrants suggest that a high proportion of birds in the migrant group permanently emigrated from our study sites. Considered together, our analyses suggest that hummingbirds in both northern and southern California sites partake in diverse and highly plastic migratory behaviours. Our assessment elucidates the dynamics underlying idiosyncratic migratory behaviours of two species of hummingbirds, in addition to describing a framework for similar assessments of migratory behaviours using the multi-state open robust design with state uncertainty (MSORD-SU) model and single-site dynamics.</p>
Effects of pair migratory behaviour on breeding phenology and success in a partially migratory shorebird population
<p>In migratory systems, variation in individual phenology can arise through differences in individual migratory behaviours, and this may be particularly apparent in partial migrant systems, where migrant and resident individuals are present within the same population. Links between breeding phenology and migratory behaviour or success are generally investigated at the individual level. However, for breeding phenology in particular, the migratory behaviours of each member of the pair may need to be considered simultaneously, as breeding phenology will likely be constrained by timing of the pair member that arrives last, and carry-over effects on breeding success may vary depending on whether pair members share the same migratory behaviour or not. We used tracking of marked individuals and monitoring of breeding success from a partially migrant population of Eurasian oystercatchers (Haematopus ostralegus) breeding in Iceland to test whether (a) breeding phenology varied with pair migratory behaviour; (b) within-pair consistency in timing of laying differed among pair migratory behaviours; and (c) reproductive performance varied with pair migratory behaviour, timing of laying and year. We found that annual variation in timing of laying differed among pair migratory behaviours, with resident pairs being more consistent than migrant and mixed pairs, and migrant/mixed pairs breeding earlier than residents in most years but later in one (unusually cold) year. Pairs that laid early were more likely to replace their clutch after nest loss, had higher productivity and higher fledging success, independent of pair migratory behaviour. Our study suggests that the links between individual migratory behaviour and reproductive success can vary over time and, to a much lesser extent, with mate migratory behaviour and can be mediated by differences in laying dates. Understanding these cascading effects of pair phenology on breeding success is likely to be key to predicting the impact of changing environmental conditions on migratory species.</p>
Data and R computer code from: Summer elk calf survival in a partially migratory population
<p>These data and computer code (written in R, https://www.r-project.org) were created to statistically evaluate a suite of intrinsic and extrinsic risk factors related to calf elk and their mothers' body condition and age. Specifically, known-fate data were collected from 94 elk calves monitored from 2013-2016 in a partially migratory elk (<em>Cervus</em> <em>canadensis</em>) population in Alberta, Canada. Along with adult female data on pregnancy status, age, and body condition, we created a time-to-event dataset that allowed us to analyze calf mortality risk in a time-to-event approach. We also estimated pooled survivorship and cause-specific mortality, as well as stratifying these metrics by migration tactic (resident vs. eastern migrant). Cox proportional hazards models were used to evaluate calf mortality risk in terms of forage biomass (kg/ha), bear predation risk (from an RSF), and other factors that varied between migration tactics. We tested for differences in a number of maternal reproductive parameters (e.g., pregnancy status) and for calf explanatory variables between migrant and resident elk segments. We also use cumulative incidence functions to estimate cause-specific mortality in this multiple carnivore system. Ultimately, we hope that this work helps wildlife managers anticipate how elk calf survival and partial migration dynamics are affected by grizzly bear predation, and our study builds on a long-term partial migration study at the Ya Ha Tinda Ranch in Alberta, Canada. </p>
Data from: Migratory singers dynamically overlap the signal space of a breeding warbler community
<p>Migratory species inhabit many communities along their migratory routes. Across taxa, these species repeatedly move into and out of communities, interacting with each other and locally breeding species and competing for resources and niche space. However, their influence is rarely considered in analyses of ecological processes within the communities they temporarily occupy. Here, we explore the impact of migratory species on a breeding community using the framework of acoustic signal space, a limited resource in which sounds of species within communities co-exist. Migrating New World warblers (Parulidae, hereafter referred to as migrant species) often sing during refueling stops in areas and at times during which locally breeding warbler species (hereafter breeding species) are singing to establish territories and attract mates. We used eBird data to determine co-occurrence of 19 migrant and 11 breeding warbler species across spring migration in SW Michigan, generated a signal space from song recordings of these species, and examined patterns of signaling overlap experienced by breeding species as migrants moved through the community. Migrant species were present for two-thirds of the breeding season of local species, including periods when breeding species established territories and attracted mates. Signaling niche overlap experienced by individual breeding species was idiosyncratic and varied over time, yet niche overlap between migrant and breeding species occurred more commonly than between breeding species or between migrant species. Nevertheless, the proportion of niche overlap between migrant and breeding warblers was similar to overlap among breeding species. Our findings showed that singing by migrant species overlapped the signals of many breeding species, suggesting that migrants could have unexplored impacts on communication in breeding species, potentially affecting song detection and song evolution. Our study contributes to a growing body of research documenting impacts of migratory species on communities and ecosystems.</p>
Figure 1. A in Survey of the Non-Migratory Birds of the Rock Islands Southern Lagoon World Heritage Site in Palau
Figure 1. A. Map of Palau. B. Map of the island groups of the Rock Islands Southern Lagoon World Heritage Site study area (inset). Our survey included all 10 island groups. Scale marker = 5 km..
Data from: Evidence for seasonal compensation of hunting mortalities in a long-lived migratory bird
<p>Understanding whether hunting mortality is additive to or compensated by other mortality sources is at the heart of managing harvested populations. Long-lived species are expected to exhibit hunting mortality additive to other sources of mortality, making them ideal candidates for population management through sport harvest. Previous studies on these processes have focussed on density-dependent natural mortality compensating for hunting mortality, but when harvest occurs in distinct periods of the year, heterogeneity in hunting vulnerability between individuals could also lead to compensatory mortality between these periods. We explore this new idea using the case of the greater snow goose (<em>Anser caerulescens atlantica</em>), a harvested species whose population became overabundant in the late 20<sup>th</sup> century. To control this population, wildlife agencies liberalized hunting regulations with unprecedented actions such as special hunting seasons implemented in spring 1999 in Canada and in winter 2009 in the USA. To determine the relative impact of each measure on survival, we estimated survival of adult geese on a seasonal basis using 30 years of capture-mark-reencounter data in a joint live-and-dead-encounter multievent model. We also used this quasi-experimental set-up to evaluate possible compensation in hunting mortality between seasons. We found that both special hunting seasons decreased goose survival in the seasons and periods in which they were implemented. However, survival increased during the spring hunting season after the establishment of the special winter hunting season in the USA in 2009. There was a negative relationship between annual spring and winter mortalities, suggesting that the increase in hunting mortality in winter was compensated by a reduction in spring mortality after 2009.</p> <p><em>Synthesis and applications:</em> To our knowledge, we report the first documented instance of hunting mortality in one season being compensated by a reduction in hunting mortality in a subsequent season. We suggest that heterogeneity in hunting vulnerability among individuals, possibly linked to the presence of juveniles, may explain this phenomenon. A better knowledge of seasonal patterns and relationships between mortality components is needed to improve our understanding of population dynamics and management of harvested populations.</p>
Fig. 6 in The Migratory Fattening Of The Barn Swallow Hirundo Rustica In Hungary
Fig. 6. Map of recoveries south from Hungary in Europe during autumn (July–November, circles) and spring (March–May, squares)
Data from: Ontogeny of migration destination, route and timing in a partially migratory bird
<p><strong>Abstract</strong></p> <ol> <li>In migratory animals, the developmental period from inexperienced juveniles to breeding adults could be a key life stage in shaping population migration patterns. Nevertheless, the development of migration routines in early life remains underexplored. While age-related changes in migration routes and timing have been described in obligate migrants, most investigations into the ontogeny of partial migrants only focused on age-dependency of migration as a binary tactic (migrant or resident), and variations in routes and timing among individuals classified as ‘migrants’ is rarely considered. </li> <li>To fill this gap, we study the ontogeny of migration destination, route and timing in a partially migratory red kite (<em>Milvus milvus</em>) population. Using an extensive GPS-tracking dataset (292 fledglings and 38 adults, with 1 – 5 migrations tracked per individual), we studied how 9 different migration characteristics changed with age and breeding status in migrant individuals, many of which become resident later in life.</li> <li>Individuals departed later from and arrived earlier at the breeding areas as they aged, resulting in a gradual prolongation of stay in the breeding area by two months from the first to the fifth migration. Individuals delayed southward migration in the year prior to territory acquirement, and they further delayed it after occupying a territory. Migration routes became more direct with age. Individuals were highly faithful to their wintering site. Migration distance shortened only slightly with age and was more similar among siblings than among unrelated individuals.</li> <li>The large gradual changes in northward and southward migrations suggest a high degree of plasticity in temporal characteristics during the developmental window. However, the high wintering site fidelity points towards large benefits of site familiarity, prompting spatial migratory plasticity to be expressed through a switch to residency. </li> <li>The contrasting patterns of trajectories of age-related changes between spatial and temporal migration characteristics might reflect different mechanisms underlying the expression of plasticity. Investigating such patterns among species along the entire spectrum of migration tactics would enable further understanding of the plastic responses exhibited by migratory species to rapid environmental changes.</li> </ol>
Fig. 3 in The roles of marginal lagoons in the maintenance of genetic diversity in the Brazilian migratory fishes Prochilodus argenteus and P. costatus
Fig. 3. Dendrogram representing the chord genetic distance among sampling groups of Prochilodus costatus. ABAr = rio Abaeté at rainy season; PAR = rio Paracatu lagoons; SFR = rio São Francisco lagoons; TMDd = Três Marias Dam at dry season; TMDr = Três Marias Dam at rainy season.
Fig. 2 in The roles of marginal lagoons in the maintenance of genetic diversity in the Brazilian migratory fishes Prochilodus argenteus and P. costatus
Fig. 2. Dendrogram representing the chord genetic distance among sampling groups of Prochilodus argenteus. ABAr = rio Abaeté at rainy season; CAR = rio Carinhanha lagoons; JEQ = rio Jequitaí lagoons; PAR = rio Paracatu lagoons; SFR = rio São Francisco lagoons; URU = rio Urucuia lagoons; VEL = rio das Velhas lagoons; TMDd = Três Marias Dam at dry season; TMDr = Três Marias Dam at rainy season.
Fig. 1 in The roles of marginal lagoons in the maintenance of genetic diversity in the Brazilian migratory fishes Prochilodus argenteus and P. costatus
Fig. 1. Map showing the central portion of the rio São Francisco basin and the distribution of the samples of Prochilodus argenteus (yellow) and of P. costatus (black). The circles represent marginal lagoons from tributaries, squares represent marginal lagoons from the rio São Francisco, and triangles represent places in the mainstream rio São Francisco in the Três Marias region. ABA = rio Abaeté; CAR = rio Carinhanha lagoons; JEQ = rio Jequitaí lagoons; PAR = rio Paracatu lagoons; SFR = rio São Francisco lagoons; URU = rio Urucuia lagoons; VEL = rio das Velhas lagoons; TMD = Três Marias Dam.
Figure 2 in Fine-scale abundance variation in New Zealand migratory and non-migratory Galaxias fish species
Figure 2. – Boxplot showing the abundance of migratory (galbre; Galaxias brevipinnis) and non-migratory (galpau; G. paucispondylus and galvul; G. vulgaris) species at sites upstream of lakes (n = 18) and sites without lakes (n = 8). Boxplots show medians (horizontal line), 25th and 75th percentiles (upper and lower box limits), maximum and minimum values (bars), and mean (red dots). Outliers are presented by black circles.
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.