Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
1,029
datasets available to search
ShareScore release 0.7.1
Dataset results
1,029 results for “altitude”
FIGURES 1–4 in Two new high-altitude species of the genus Omphreus Dejean (Coleoptera: Carabidae: Harpalinae) from Serbia
FIGURES 1–4. Omphreus (Omphreus) ovcarensis n. sp. from the village of Ovċar Banja, Mt. Ovċar, Serbia. 1—holotype male, habitus (dorsal view); 2—holotype male, aedeagus (dorsal view); 3—holotype male, aedeagus (lateral view); 4—paratype female, genitalia. Scale lines 1.00 mm.
FIGURES 5–9 in Two new high-altitude species of the genus Omphreus Dejean (Coleoptera: Carabidae: Harpalinae) from Serbia
FIGURES 5–9. Omphreus (Omphreus) serbooccidentalis n. sp. from the village of Mrċiċi, Bukovi Peak, Mt. Maljen, Serbia. 5—holotype male, habitus (dorsal view); 6—holotype male, aedeagus (dorsal view); 7—holotype male, aedeagus (lateral view); 8—paratype female, genitalia; 9—holotype male, abdominal sternite IX (urite). Scale lines 1.00 mm.
Sentinel-2 derived Chlorophyll-a prediction maps for high-altitude lakes in the Sierra Nevada, Spain
<p>This dataset contains chlorophyll-a (ug/L) predictions for 4 high-altitude lakes in the Sierra Nevada Mountain Range, Spain. Predictions were made using a simple linear regression model with field sample chlorophyll-a as the dependent variable, and the following Sentinel-2 derived spectral index as the independent variable:</p><p>B3 - (B4+((B2-B4)*((665-560)/(665-490)))</p><p>Prediction maps are included as GeoTiffs and NetCDF files. Sentinel-2 data were atmospherically corrected using the following algorithms: </p><ul><li><a href="https://github.com/acolite/acolite/releases/tag/20221114.0">ACOLITE</a> (<a href="https://doi.org/10.1016/j.rse.2018.07.015">Vanhellemont & Ruddick, 2018</a>)</li><li><a href="https://grass.osgeo.org/grass83/manuals/i.atcorr.html">6SV</a> (<a href="https://doi.org/10.1109/36.581987">Vermote et al. 2006</a>)</li></ul><p><strong>Included Lakes and and their IDs:</strong></p><ul><li>Laguna de la Caldera (ID = P-2)</li><li>Laguna-embalse de las Yeguas (ID = D-6)</li><li>Laguna de Río Seco (ID = P-8)</li><li>Laguna Larga (ID = G-7)</li></ul>
Fig. 2 in Altitudinal Distribution of Aquatic Beetles (Coleoptera) in Northern Tunisia: Relationship between Species Richness and Altitude
Fig. 2. Relationship between number of sampling sites and species richness at three altitudinal levels. 1 = 1–249 m;
supplément à "Modélisation des régimes thermiques du sol dans les milieux ouverts d'altitude des Alpes françaises : influence du transport de neige par le vent et de la végétation" : codes et données
<p>Codes et données pour reproduire les chapitres 2 et 5 de la thèse de Matthieu Baron intitulée "Modélisation des régimes thermiques du sol dans les milieux ouverts d'altitude des Alpes françaises : influence du transport de neige par le vent et de la végétation".</p><p>Les jeux de données incluent nottamment:</p><p> - des sorties de simulations de SURFEX</p><p> - des données de températures du sol extraites dans le cadre de différents projets de la Zone Atelier Alpes et retravaillées. Une autre version de ces données (plus actuelle) est publiée ici :</p><p>CHOLER, Philippe; SAGOT, Clotilde; AUGE, Vincent; DENTANT, Cédric; réseau Flore Sentinelle; LIGER, Lucie; MANSONS, Jérôme; NAPOLEONI, Raphaëlle; SAILLARD, Amélie; TILL BOTTRAUD, Irène; FORT, Noémie, 2023, "Long term monitoring of near surface soil temperature in the french Alps", <a href="https://doi.org/10.57745/JOZ1NA">https://doi.org/10.57745/JOZ1NA</a>, Recherche Data Gouv, V1</p><p> </p><p>Un fichier README.md est présent dans la racine du dossier et donne une desription plus poussée de son contenu </p>
Investigation of cirrus clouds properties in the Tropical Tropopause Layer using high-altitude limb scanning near-IR spectroscopy during the NASA-ATTREX Experiment
<p>Data results of the findings of the AMT-2023-85 research article, titled: "Investigation of cirrus clouds properties in the Tropical Tropopause Layer using high-altitude limb scanning near-IR spectroscopy during the NASA-ATTREX Experiment", submitted to the Atmospheric Measurement Techniques journal on 20 Apr 2023.</p>
Interactions and Multifrequency Radiation Characteristics of Bidirectional Leaders in Altitude-Triggered Lightning
<p><span>Altitude-triggered lightning provides favorable conditions for the research of bidirectional leader system. In the summer of 2023, altitude-triggered lightning experiment was conducted on the Field Experiment Base on Lightning Sciences, China Meteorological Administration. <a name="_Hlk162343222"></a>The multifrequency radiation characteristics of bidirectional leaders and the interactions of both ends during the propagation are analyzed. Specifically, the discharge processes relevant to LF-MF magnetic radiations of bidirectional leaders can be revealed by high-speed optical images in altitude-triggered lightning, and all these LF-MF radiations correspond to VHF radiations associated with bidirectional leaders well. Unlike the close correlation between the LF-MF radiation strengths and the discharge intensities, <a name="OLE_LINK10"></a>the VHF radiation strengths vary greatly even for similar discharge events, since VHF radiations correspond to microscopic random breakdown processes. Furthermore, the changes of leader speed and channel brightness before and after the bidirectional leaders indicate that <span>the development of the two ends of bidirectional leads is mutually reinforcing.</span></span></p>
HighResClimNevada: a high-resolution climatological dataset for a high-altitude region in Southern Spain (Sierra Nevada)
<p>Codes and data made available as part of the data paper "HighResClimNevada: a high-resolution climatological dataset for a high-altitude region in Southern Spain (Sierra Nevada)" publication. This work presents the HighResClimNevada database, a climatic database for Sierra Nevada (southern Spain) based on data modeled with the Weather Research and Forecasting model. The data used as a reference for the evaluation of HighResClimNevada are freely available online at the websites of the different institutions that develop it, so they are not available here.</p> <p>This research was financially supported by the project "Plan Complementario de I+D+i en el área de Biodiversidad (PCBIO)" funded by the European Union within the framework of the Recovery, Transformation and Resilience Plan - NextGenerationEU and by the Regional Government of Andalucia, the project PID2021-126401OB-I00, funded by MICIU/AEI/10.13039/501100011033 and by FEDER, UE; and LifeWatch-2019-10-UGR-01 co-funded by the Ministry of Science and Innovation through the FEDER funds from the Spanish Pluriregional Operational Program 2014–2020 (POPE) LifeWatch-ERIC action line; and P20_00035 funded by FEDER/Junta de Andalucía-Consejería de Transformación Económica, Industria, Conocimiento y Universidades.</p>
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest. in Suidae
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest.
FIGURE 6. Hyphinomos svenhedini Ramme, 1950 in Revision of the high-altitude genus Hyphinomos Uvarov, 1921 (Orthoptera: Tettigoniidae) with a redescription and new data on mating behavior and acoustic signals of H. svenhedini Ramme, 1950
FIGURE 6. Hyphinomos svenhedini Ramme, 1950 (A) female head, pronotum and forewing, (B) male head, pronotum and forewing, (C) maxillary palpi, (D) female head and pronotum, (E) front view of face and (F) top view of fore tibia showing external and internal tympanum. Scale 5mm.
FIGURE 1 in Revision of the high-altitude genus Hyphinomos Uvarov, 1921 (Orthoptera: Tettigoniidae) with a redescription and new data on mating behavior and acoustic signals of H. svenhedini Ramme, 1950
FIGURE 1. Map showing type localities of Hyphinomos fasciata Uvarov, 1921 (in Dakar, Western Tibet, China) and H. svenhedini Ramme, 1950 (in Hanle, Indus Valley, Ladakh and Lahaul, Himachal Pradesh, India). Zanskar and Shashi lake, Kargil, Ladakh are additional locations from where H. svenhedini has been reported. Area highlighted in green is Ladakh, U.T., pink: Kargil district of Ladakh, blue: Lahaul and Spiti district in Himachal Pradesh.
FIGURE 12 in Revision of the high-altitude genus Hyphinomos Uvarov, 1921 (Orthoptera: Tettigoniidae) with a redescription and new data on mating behavior and acoustic signals of H. svenhedini Ramme, 1950
FIGURE 12. Male and female of Hyphinomos svenhedini Ramme, 1950 (A) exhibiting end-to-end copulation position in laboratory condition and (B) in natural habitat.
FIGURE 5. Hyphinomos svenhedini Ramme, 1950 in Revision of the high-altitude genus Hyphinomos Uvarov, 1921 (Orthoptera: Tettigoniidae) with a redescription and new data on mating behavior and acoustic signals of H. svenhedini Ramme, 1950
FIGURE 5. Hyphinomos svenhedini Ramme, 1950 (A & B) female and (C & D) male in dorsal and lateral view respectively. Scale 14mm.
FIGURE 9 in Revision of the high-altitude genus Hyphinomos Uvarov, 1921 (Orthoptera: Tettigoniidae) with a redescription and new data on mating behavior and acoustic signals of H. svenhedini Ramme, 1950
FIGURE 9. Variation in the shape and number of teeth present in the anal cerci between three males of Hyphinomos svenhedini Ramme, 1950 from Shashi lake. Two image panels show anal cerci of left and right sides of same individual.
FIGURE 8. Hyphinomos svenhedini Ramme, 1950 in Revision of the high-altitude genus Hyphinomos Uvarov, 1921 (Orthoptera: Tettigoniidae) with a redescription and new data on mating behavior and acoustic signals of H. svenhedini Ramme, 1950
FIGURE 8. Hyphinomos svenhedini Ramme, 1950 (A) apical view of male abdomen, (B) lateral view of male supra anal and subgenital plate, (C) dorsal view of male supra anal plate, (D) dorsal view of male subgenital plate, (E) dorsal view of female subgenital plate and (F) female supra anal plate. Scale 1mm.
FIGURE 7. Hyphinomos svenhedini Ramme, 1950 in Revision of the high-altitude genus Hyphinomos Uvarov, 1921 (Orthoptera: Tettigoniidae) with a redescription and new data on mating behavior and acoustic signals of H. svenhedini Ramme, 1950
FIGURE 7. Hyphinomos svenhedini Ramme, 1950 (A) right side forewing in ventral view showing stridulatory file present on PCuA, Scale 1mm and (B)scanning electron micrograph of the stridulatory teeth, Scale 10μm.
FIGURE 4. Hyphinomos svenhedini Ramme, 1950 in Revision of the high-altitude genus Hyphinomos Uvarov, 1921 (Orthoptera: Tettigoniidae) with a redescription and new data on mating behavior and acoustic signals of H. svenhedini Ramme, 1950
FIGURE 4. Hyphinomos svenhedini Ramme, 1950 showing body coloration in live condition (A) dorsal view of male in its natural habitat near Shashi lake, (B) front view of male and (C) dorsal view of young female in its natural habitat near Shashi lake.
FIGURE 3 in Revision of the high-altitude genus Hyphinomos Uvarov, 1921 (Orthoptera: Tettigoniidae) with a redescription and new data on mating behavior and acoustic signals of H. svenhedini Ramme, 1950
FIGURE 3. Ovipositor shape of Hyphinomos svenhedini Ramme, 1950 (A) Allotype, (B) Paratype from NMW, (C) studied specimen from Shashi lake and (D) Paratype of H. fasciata Uvarov, 1921 from MNCN (photo from OSF).
FIGURE 14 in Revision of the high-altitude genus Hyphinomos Uvarov, 1921 (Orthoptera: Tettigoniidae) with a redescription and new data on mating behavior and acoustic signals of H. svenhedini Ramme, 1950
FIGURE 14. Oscillograms (A–B) and spectrogram (C) of Hyphinomos svenhedini Ramme, 1950 'courtship' song recorded in laboratory.
FIGURE 13 in Revision of the high-altitude genus Hyphinomos Uvarov, 1921 (Orthoptera: Tettigoniidae) with a redescription and new data on mating behavior and acoustic signals of H. svenhedini Ramme, 1950
FIGURE 13. Oscillograms (A–B) and spectrogram (C) of Hyphinomos svenhedini Ramme, 1950 long-distance calling song recorded in laboratory.
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.