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.
42
datasets available to search
ShareScore release 0.9.0
Dataset results
42 results for “North Pacific Coast”
Рис. 2. Распредение биомассы Mytilus trossulus septentrionalis на литорали дальневоcточных морей России. Здесь и далее на гистограммах по оси абцисс после географических пунктов в скобках укаЗана выборка (число иЗученных проб), по оси ординат – максимальные ЗначениЯ биомассы вида. Под Значением биомассы 0.1 г/м² подраЗумеваютсЯ качественные пробы. СокраЩениЯ (бмп) и (топ) оЗначают соответственно беринговоморское и тихоокеанское побережьЯ Восточной Камчатки. Побережье Зал. Петра Великого от устьЯ р. Туманной к северу до м. Поворотного условно отноcитсЯ к южному Приморью; побережье к северу от м. Поворотного (пос. Преображение, б. СоколовскаЯ) до б. Ольга, включительно, условно относитсЯ к среднему Приморью; побережье к северу от б. Ольга до м. Белкина и материковое побережье Татарского пролива относим к северному Приморью. Fig. 2. The distribution of biomass of Mytilus trossulus septentrionalis in the intertidal zone of the Far Eastern seas of Russia. Here and throughout on histograms, on the abcissa is the number of studied samples (numbers in parentheses following the names geographic localities), on the ordinate is the maximum biomass of species. The number 0.1 g wet wt m-2 means the qualitative samples. Abbreviations (bmp) and (top) mean the Bering Sea coast and the Pacific coast of eastern Kamchatka. The coast of Peter the Great Bay from the mouth of the Tumannaya River to Cape Povorotny is conditionally referred to as southern Primorye; the area north of Cape Povorotny (Preobrazhenie Settlement, Sokolovskaya Bay) to Olga Bay inclusive is conditionally referred to as middle Primorye; north of Olga Bay to Cape Belkin and the mainland coast of the Tatar Strait to as northern Primorye. in Bivalve mollusks of the intertidal zone of the Far Eastern seas of Russia
Рис. 2. Распредение биомассы Mytilus trossulus septentrionalis на литорали дальневоcточных морей России. Здесь и далее на гистограммах по оси абцисс после географических пунктов в скобках укаЗана выборка (число иЗученных проб), по оси ординат – максимальные ЗначениЯ биомассы вида. Под Значением биомассы 0.1 г/м² подраЗумеваютсЯ качественные пробы. СокраЩениЯ (бмп) и (топ) оЗначают соответственно беринговоморское и тихоокеанское побережьЯ Восточной Камчатки. Побережье Зал. Петра Великого от устьЯ р. Туманной к северу до м. Поворотного условно отноcитсЯ к южному Приморью; побережье к северу от м. Поворотного (пос. Преображение, б. СоколовскаЯ) до б. Ольга, включительно, условно относитсЯ к среднему Приморью; побережье к северу от б. Ольга до м. Белкина и материковое побережье Татарского пролива относим к северному Приморью. Fig. 2. The distribution of biomass of Mytilus trossulus septentrionalis in the intertidal zone of the Far Eastern seas of Russia. Here and throughout on histograms, on the abcissa is the number of studied samples (numbers in parentheses following the names geographic localities), on the ordinate is the maximum biomass of species. The number 0.1 g wet wt m-2 means the qualitative samples. Abbreviations (bmp) and (top) mean the Bering Sea coast and the Pacific coast of eastern Kamchatka. The coast of Peter the Great Bay from the mouth of the Tumannaya River to Cape Povorotny is conditionally referred to as southern Primorye; the area north of Cape Povorotny (Preobrazhenie Settlement, Sokolovskaya Bay) to Olga Bay inclusive is conditionally referred to as middle Primorye; north of Olga Bay to Cape Belkin and the mainland coast of the Tatar Strait to as northern Primorye.
Fig. 8 in A new species of saurolophine hadrosaurid dinosaur from the Late Cretaceous of the Pacific coast of North America
Fig. 8. Single most parsimonious tree derived from maximum parsimony analysis of 49 hadrosauroid species, highlighting the position of Saurolophus morrisi sp. nov. within saurolophine hadrosaurids. Numbers above the branches indicate decay indices (Bremer support), whereas those below indicate bootstrap frequencies. Lambeeosaurinae is collapsed into a single branch for clarity; lambeosaurine interrelationships recovered were identical to those in Fig. 7.
Fig. 1 in A new species of saurolophine hadrosaurid dinosaur from the Late Cretaceous of the Pacific coast of North America
Fig. 1. Partial right postorbital of a hadrosaurid dinosaur Saurolophus morrisi sp. nov. (LACM/CIT 2852), lower Maastrichtian Moreno Formation of San Benito County, California, USA, showing the autapomorphic ornamentation of its jugal process. Posterior (A) and right lateral (B) views.
Fig. 5 in A new species of saurolophine hadrosaurid dinosaur from the Late Cretaceous of the Pacific coast of North America
Fig. 5. Appendicular elements of a hadrosaurid dinosaur Saurolophus morrisi sp. nov. (LACM/CIT 2760, a subadult), lower Maastrichtian Moreno Formation of Panoche Hills, Fresno County, California, USA. A. Partial left scapula and coracoid in lateral view. B. Partially articulated forelimb elements. C. Proximal segment of right tibia in lateral view. D. Distal fragments of femora. E. Right metatarsal III in dorsal view.
Fig. 3 in A new species of saurolophine hadrosaurid dinosaur from the Late Cretaceous of the Pacific coast of North America
Fig. 3. Right posterolateral view of the frontal of a hadrosaurid dinosaur Saurolophus morrisi sp. nov. (LACM/CIT 2760, a subadult), lower Maastrichtian Moreno Formation of Panoche Hills, Fresno County, California, USA, showing the eroded remnant of the buttressing base of the posterodorsal frontal ramus.
Fig. 7 in A new species of saurolophine hadrosaurid dinosaur from the Late Cretaceous of the Pacific coast of North America
Fig. 7. Strict consensus tree of the three most parsimonious trees derived from maximum parsimony analysis of 49 hadrosauroid species. LACM/CIT 2760 and 2852 were coded as separate OTUs and their position within Saurolophinae in highlighted in the cladogram. Numbers above the branches indicate decay indices (Bremer support), whereas those below indicate bootstrap frequencies.
Fig. 9 in A new species of saurolophine hadrosaurid dinosaur from the Late Cretaceous of the Pacific coast of North America
Fig. 9. Comparison of the general skull and premaxillary morphology of two hadrosaurid dinosaurs Saurolophus osborni Brown, 1912, holotype AMNH 5220 (A) and Saurolophus morrisi sp. nov., holotype LACM/CIT 2852 (B), highlighting characters shared by these two taxa. Skull in right lateral view (A1, B1), right premaxilla in lateral view (A2, B2).The white inscription on the premaxilla denote the abbreviation for that bone, painted by the curatorial staff back in the early twentieth century.
Fig. 6 in A new species of saurolophine hadrosaurid dinosaur from the Late Cretaceous of the Pacific coast of North America
Fig. 6. Appendicular elements of a hadrosaurid dinosaur Saurolophus morrisi sp. nov. (LACM/CIT 2852), lower Maastrichtian Moreno Formation of San Benito County, California, USA. A. Partial right scapula in lateral view. B. Right ulna in lateral view and possible manual phalanx II−1 in dorsal view. C. Right metatarsal III in dorsal (C1) and lateral (C2) views.
Fig. 2 in A new species of saurolophine hadrosaurid dinosaur from the Late Cretaceous of the Pacific coast of North America
Fig. 2. Partial skull roof of a hadrosaurid dinosaur Saurolophus morrisi sp. nov. (LACM/CIT 2760, a subadult), lower Maastrichtian Moreno Formation of Panoche Hills, Fresno County, California, USA. Dorsal (A) and ventral (B) views. Photographs (A1, B1) and interpretative drawings (A2, B2).
Long-term change in the parasite burden of shore crabs (Hemigrapsus oregonensis and H. nudus) on the northwestern Pacific coast of North America
Open the record for dataset details and reuse information.
MIS 5e relative sea-level index points along the Pacific coast of North America
<p>This spreadsheet contains data and metadata on relative sea-level index points and associated ages for the Pacific coast of North America. This is Version 1.1, updated after the peer-review of the associated paper.</p>
FIGURE 1 in New Zealand exports: Pseudosphaeroma Chilton, 1909 (Isopoda: Sphaeromatidae), a Southern Hemisphere genus introduced to the Pacific coast of North America
FIGURE 1. Pseudosphaeroma sp. All figs of specimens from Millerton Point, Tamales Bay, Marin County, California (RW02.022). All figs of male except B and E, female.
FIGURE 2 in New Zealand exports: Pseudosphaeroma Chilton, 1909 (Isopoda: Sphaeromatidae), a Southern Hemisphere genus introduced to the Pacific coast of North America
FIGURE 2. Pseudosphaeroma campbellense. Male (6.2 mm) syntype. A, lateral view; B, dorsal view of pleon and pleotelson; C, epistome; D, uropod.
Distribution. Endemic to N Pacific Ocean, the majority ofrecords come from W North America from 32° 42° N to 54° 18' N, also recorded on the Pacific coast ofJapan from 35% to 41° 42° N. This suggests that distribution of this species spans the N Pacific Ocean, but with no records from the C Pacific Ocean, it remains possible that there are separate E and W populations. It has been suggested that distribution of this species is related to the deep current system of the subarctic. in Ziphiidae
Distribution. Endemic to N Pacific Ocean, the majority ofrecords come from W North America from 32° 42° N to 54° 18' N, also recorded on the Pacific coast ofJapan from 35% to 41° 42° N. This suggests that distribution of this species spans the N Pacific Ocean, but with no records from the C Pacific Ocean, it remains possible that there are separate E and W populations. It has been suggested that distribution of this species is related to the deep current system of the subarctic.
Distribution. NE Pacific, Aleutian Is, Gulf of Alaska, and W coast of North America S to C Baja California (Mexico); occasionally to Hawaiian Is and Japan, and into the Bering Sea. in Phocidae
Distribution. NE Pacific, Aleutian Is, Gulf of Alaska, and W coast of North America S to C Baja California (Mexico); occasionally to Hawaiian Is and Japan, and into the Bering Sea.
Subspecies and Distribution. P.m.maniculatusWagner,1845—SManitoba,Ontario,Quebec,andLabrador,Canada. P.m.abietorumBangs,1896—NewBrunswickandNovaScotia,Canada,andMaine, USA. P.m.alpinusCowan,1937—restrictedtoasmallregioninSEBritishColumbia,Canada . P.m.anacapaevonBloeker,1942—knownonlyfromWestAnacapaIandsurroundingIs,California,USA. P.m.angustusHall,1932—knownonlyfromSWpartofVancouverI,BritishColumbia, Canada. P.m.anticostiensisMoulthrop,1937—knownonlyfromthetypelocalityonEAnticostiI,Quebec,Canada. P.m.argentatusCopeland&Church,1906—knownonlyfromthetypelocalityonGrandMananI,NewBrunswick,Canada. P.m.artemisiaeRhoads,1894—fromSCBritishColumbia,Canada,SWtoWWyoming, USA. P.m.assimilisNelson&Goldman,1931—knownonlyfromthetypelocalityonCoronadoIs,BajaCalifornia,Mexico. P.m.austerusBaird,1855—WCWashington,USA. P.m.bairdiiHoy&Kennicott,1857—mostoftheECportionoftheUSA. P.m.balaclavaeMcCabe&Cowan,1945—knownonlyfromthetypelocalityonBalaklavaI,BritishColumbia,Canada. P.m.blandusOsgood,1904—SCUSAStoSanLuisPotosi,Guanajauto,andJalisco, Mexico. P.m.borealisMearns,1911—NWCanada. P.m.catalinaeElliot,1903—knownonlyfromSantaCatalinaI,California,USA. P.m.cmenitius|.A.Allen,1898—knownonlyfromthetypelocalityonSanRoqueI, BajaCalifornia,Mexico. P.m.clementisMearns,1896—knownonlyfromSanClementeI,California,USA. P.m.coolidge:Thomas,1898—SBajaCaliforniaandBajaCaliforniaSur,Mexico. P.m.dorsalisNelson&Goldman,1931—knownonlyfromthetypelocalityonNatividadI,BajaCalifornia,Mexico. P.m.dubiusJ.A.Allen,1898—knownonlyfromthetypelocalityonTodosSantosI, BajaCalifornia,Mexico. P.m.elususNelson&Goldman,1931—knownonlyfromSantaBarabaraandSutilIs, California,USA. P.m.eremusOsgood,1909—knownonlyfromGrindstoneI,Quebec,Canada. P.m.exiguusJ.A.Allen,1898—knownonlyfromSanMartinI,BajaCalifornia,Mexico. P.m.exterusNelson&Goldman,1931—knownonlyfromthetypelocalityonSanNicolasI,California,USA. P.m.fulvusOsgood,1904—fromCPueblaandVeracruzStoCOaxaca,Mexico. P.m.gambeliiBaird,1858—N&WCalifornia,USA,SintoNBajaCalifornia,Mexico. P.m.georgiensisHall,1938—knownonlyfromthetypelocalityonTexadaIandsurroundingIs,BritishColumbia,Canada. P.m.geronimensisJ.A.Allen,1898—knownonlyfromthetypelocalityonSanGeronimoI,BajaCalifornia,Mexico. P.m.gracilisLeConte,1855—OntarioandSQuebec,Canada,S&EtoWisconsin, Michigan,andNEUSA.FP.m.hollister:Osgood,1909—knownonlyfromSanJuanIandsurroundingIs,Washington,USA. P.m.huey:Nelson&Goldman,1932—knownonlyfromthetypelocalityonasmallunnamedIinGonzagaBay,BajaCalifornia,Mexico. P. m. inclarus Goldman, 1939 — known only from Fremont I in Great Salt Lake, Utah, USA. P.m. labecula Elliot, 1903 — from Durango S to Michoacan and Morelos, Mexico. P. m. luteus Osgood, 1905 — from South Dakota S to W Texas, USA. P. m. magdalenae Osgood, 1909 — Magdalena I and surrounding mainland areas, Baja California, Mexico. P.m. margaritae Osgood, 1909 — known only from Margarita I, Baja California, Mexico. Pm. nebrascensis Coues, 1877 — from S Alberta and Saskatchewan, Canada, S to NW Texas, USA. Pm. nubiterrae Rhoads, 1896 — from W New York S to North Carolina, USA. Pm. ozarkiarum Black, 1935 — from NE Oklahoma and SW Missouri S to W Arkansas and NC edge of Texas, USA. P. m. pallescensJ. A. Allen, 1896 — NC to SC Texas, USA. Pm. plumbeus C. F. Jackson, 1939 — E Quebec, Canada. Pm. rubidus Osgood, 1901 — from SW Washington S along the Pacific Coast to C California, USA. P. m. rufinus Merriam, 1890 — from N California S to SC Arizona and New Mexico, USA. P. m. sanctaerosae von Bloeker, 1940 — known only from Santa Rosa I, California, USA. P.m. santacruzae Nelson & Goldman, 1931 — known only from Santa Cruz I, California, USA. Pm. saturatus Bangs, 1897 — known only from Saturna I, British Columbia, Canada. Pm. saxamans McCabe & Cowan, 1945 — known only from Duncan I and surrounding Is, British Columbia, Canada. Pm. serratus Davis, 1939 — restricted to a small region in C Idaho, USA. Pm. sonoriensis Le Conte, 1853 — from SE Oregon and S Idaho, USA, S to N edge of Sonora, Mexico. Pm. streatori Nelson & Goldman, 1931 — known only from San Miguel I and surrounding Is, California, USA. in Cricetidae
Subspecies and Distribution. P.m.maniculatusWagner,1845—SManitoba,Ontario,Quebec,andLabrador,Canada. P.m.abietorumBangs,1896—NewBrunswickandNovaScotia,Canada,andMaine, USA. P.m.alpinusCowan,1937—restrictedtoasmallregioninSEBritishColumbia,Canada . P.m.anacapaevonBloeker,1942—knownonlyfromWestAnacapaIandsurroundingIs,California,USA. P.m.angustusHall,1932—knownonlyfromSWpartofVancouverI,BritishColumbia, Canada. P.m.anticostiensisMoulthrop,1937—knownonlyfromthetypelocalityonEAnticostiI,Quebec,Canada. P.m.argentatusCopeland&Church,1906—knownonlyfromthetypelocalityonGrandMananI,NewBrunswick,Canada. P.m.artemisiaeRhoads,1894—fromSCBritishColumbia,Canada,SWtoWWyoming, USA. P.m.assimilisNelson&Goldman,1931—knownonlyfromthetypelocalityonCoronadoIs,BajaCalifornia,Mexico. P.m.austerusBaird,1855—WCWashington,USA. P.m.bairdiiHoy&Kennicott,1857—mostoftheECportionoftheUSA. P.m.balaclavaeMcCabe&Cowan,1945—knownonlyfromthetypelocalityonBalaklavaI,BritishColumbia,Canada. P.m.blandusOsgood,1904—SCUSAStoSanLuisPotosi,Guanajauto,andJalisco, Mexico. P.m.borealisMearns,1911—NWCanada. P.m.catalinaeElliot,1903—knownonlyfromSantaCatalinaI,California,USA. P.m.cmenitius|.A.Allen,1898—knownonlyfromthetypelocalityonSanRoqueI, BajaCalifornia,Mexico. P.m.clementisMearns,1896—knownonlyfromSanClementeI,California,USA. P.m.coolidge:Thomas,1898—SBajaCaliforniaandBajaCaliforniaSur,Mexico. P.m.dorsalisNelson&Goldman,1931—knownonlyfromthetypelocalityonNatividadI,BajaCalifornia,Mexico. P.m.dubiusJ.A.Allen,1898—knownonlyfromthetypelocalityonTodosSantosI, BajaCalifornia,Mexico. P.m.elususNelson&Goldman,1931—knownonlyfromSantaBarabaraandSutilIs, California,USA. P.m.eremusOsgood,1909—knownonlyfromGrindstoneI,Quebec,Canada. P.m.exiguusJ.A.Allen,1898—knownonlyfromSanMartinI,BajaCalifornia,Mexico. P.m.exterusNelson&Goldman,1931—knownonlyfromthetypelocalityonSanNicolasI,California,USA. P.m.fulvusOsgood,1904—fromCPueblaandVeracruzStoCOaxaca,Mexico. P.m.gambeliiBaird,1858—N&WCalifornia,USA,SintoNBajaCalifornia,Mexico. P.m.georgiensisHall,1938—knownonlyfromthetypelocalityonTexadaIandsurroundingIs,BritishColumbia,Canada. P.m.geronimensisJ.A.Allen,1898—knownonlyfromthetypelocalityonSanGeronimoI,BajaCalifornia,Mexico. P.m.gracilisLeConte,1855—OntarioandSQuebec,Canada,S&EtoWisconsin, Michigan,andNEUSA.FP.m.hollister:Osgood,1909—knownonlyfromSanJuanIandsurroundingIs,Washington,USA. P.m.huey:Nelson&Goldman,1932—knownonlyfromthetypelocalityonasmallunnamedIinGonzagaBay,BajaCalifornia,Mexico. P. m. inclarus Goldman, 1939 — known only from Fremont I in Great Salt Lake, Utah, USA. P.m. labecula Elliot, 1903 — from Durango S to Michoacan and Morelos, Mexico. P. m. luteus Osgood, 1905 — from South Dakota S to W Texas, USA. P. m. magdalenae Osgood, 1909 — Magdalena I and surrounding mainland areas, Baja California, Mexico. P.m. margaritae Osgood, 1909 — known only from Margarita I, Baja California, Mexico. Pm. nebrascensis Coues, 1877 — from S Alberta and Saskatchewan, Canada, S to NW Texas, USA. Pm. nubiterrae Rhoads, 1896 — from W New York S to North Carolina, USA. Pm. ozarkiarum Black, 1935 — from NE Oklahoma and SW Missouri S to W Arkansas and NC edge of Texas, USA. P. m. pallescensJ. A. Allen, 1896 — NC to SC Texas, USA. Pm. plumbeus C. F. Jackson, 1939 — E Quebec, Canada. Pm. rubidus Osgood, 1901 — from SW Washington S along the Pacific Coast to C California, USA. P. m. rufinus Merriam, 1890 — from N California S to SC Arizona and New Mexico, USA. P. m. sanctaerosae von Bloeker, 1940 — known only from Santa Rosa I, California, USA. P.m. santacruzae Nelson & Goldman, 1931 — known only from Santa Cruz I, California, USA. Pm. saturatus Bangs, 1897 — known only from Saturna I, British Columbia, Canada. Pm. saxamans McCabe & Cowan, 1945 — known only from Duncan I and surrounding Is, British Columbia, Canada. Pm. serratus Davis, 1939 — restricted to a small region in C Idaho, USA. Pm. sonoriensis Le Conte, 1853 — from SE Oregon and S Idaho, USA, S to N edge of Sonora, Mexico. Pm. streatori Nelson & Goldman, 1931 — known only from San Miguel I and surrounding Is, California, USA.
FIGURE 3 in Two new species of Laonice (Norgensia) (Spionidae, Polychaeta) from subtropical Atlantic and subequatorial Pacific coasts of North America
FIGURE 3. Laonice (Norgensia) rasmusseni sp. nov. Holotype. A. Anterior end with six chaetigers, dorsal view; B. Transdorsal membranes on chaetigers 41–43; C. Posterior end with pygidium, dorsal view; D. Anterior end with seven chaetigers, lateral view; E–G. Parapodia of chaetigers 5, 42 and 57; H–I. Hooded hook of chaetiger 40, side and frontal view. Scale: A–D—1 mm; E–G—0.5 mm; H–I—0.02 mm.
FIGURE 2 in Two new species of Laonice (Norgensia) (Spionidae, Polychaeta) from subtropical Atlantic and subequatorial Pacific coasts of North America
FIGURE 2. Laonice (Norgensia) costaricensis sp. nov. A. Anterior end, dorsal view; B. Posterior end with pygidium, ventral view; C–F. Parapodia of chaetigers 2, 7, 24 and 42; G–H. Hooded hook from chaetiger 42, side and frontal view. A–B—Holotype (MCZ 101143); C–G—Paratype (MZUCR 348-05). Scale: A–B, D–F—0.5 mm; C—0.3 mm; G—0.05 mm.
FIGURE 1 in Two new species of Laonice (Norgensia) (Spionidae, Polychaeta) from subtropical Atlantic and subequatorial Pacific coasts of North America
FIGURE 1. Laonice (Norgensia) vieitezi Lopez, 2011. Holotype—apical part of hooks: A. Single tooth above main fang. B. Paired teeth above main fang. Scale—10 µ.
Data from: Genotyping-by-sequencing reveals genomic homogeneity among overwintering Pacific Dunlin (Calidris alpina pacifica) aggregations along the Pacific coast of North America
Information on how migratory populations are genetically structured during the overwintering season of the annual cycle can improve our understanding of the strength of migratory connectivity and help identify populations as units for management. Here, we use a genotype-by-sequencing approach to investigate whether population genetic structure exists among overwintering aggregations of the Pacific Dunlin subspecies (Calidris alpina pacifica) sampled at two spatial scales (i.e. within and among overwintering sites) in the eastern Pacific Flyway. Genome-wide analyses of 874 single nucleotide polymorphisms across 80 sampled individuals revealed no evidence for genetic differentiation among aggregations overwintering at three locations within the Fraser River Estuary (FRE) of British Columbia. Similarly, comparisons of aggregations in the FRE and those overwintering in southern sites in California and Mexico indicated no genetic segregation between northern and southern overwintering areas. These results suggest that Pacific Dunlin residing within the FRE, Sacramento Valley (California) and Guerrero Negro (Mexico) are genetically homogeneous, with no evident genetic structure between sampled sites or regions across the overwintering range. Despite no evidence for differentiation among aggregations, we identified a significant effect of geographical distance between sites on the distribution of individual genotypes in a redundancy analysis; however, a small proportion of the total genotypic variance (R2 = 0.036, P = 0.011) was explained by the combined effect of latitude and longitude, suggesting weak genomic patterns of isolation-by-distance that are consistent with chain-like migratory connectivity between breeding and overwintering areas. Our study represents the first genome-scale investigation of population structure for a Dunlin subspecies and provides essential baseline estimates of genomic diversity and differentiation within the Pacific Dunlin.
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.