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FIGURE 3. Philobrya alata. A‒C, H, I, L, M in The Genus Philobrya J.G. Cooper, 1867 (Bivalvia: Philobryidae) In Patagonia And Adjacent Antarctic Waters
FIGURE 3. Philobrya alata. A‒C, H, I, L, M: holotype (MLP-Ma 15117), D‒G, K: specimens from Isla de los Estados (D‒G: MACN-In 43530, K: MACN-In 43529), J: paratype (MACN-In 43525). A, B, D‒G: outer views right valve (A: with periostracum, B, D‒G: without periostracum), C: outer view left valve (without periostracum), H: inner view left valve, I: inner view right valve, J: brooded embryo removed from the demibranch of an adult specimen, K, L: hinge plates right valve (K: specimen of 2.5 mm L, L: specimen of 2.9 mm L), M: hinge plate left valve (specimen of 2.9 mm L). Scale bars A‒I: 1 mm; J: 100 µm; K‒M: 500 µm. (Figures 3A‒C, H‒M are reproduced from Urcola & Zelaya (2021)).
FIGURE 2 in The Genus Philobrya J.G. Cooper, 1867 (Bivalvia: Philobryidae) In Patagonia And Adjacent Antarctic Waters
FIGURE 2. Orientation, measurements, and morphological and anatomical characters of Philobrya species. A: inner view left valve, B: antero-dorsal view, C: detail of the hinge plate, D: prodissoconch, E, F: periostracal projections, G‒I: gross anatomy of specimens in which the right valve was removed (G: P. quadrata, H: P. magellanica, I: P. limoides). Abbreviations: ada, antero-dorsal area; antG1b, anterior series of G1b teeth; ca, central area; G1ba, angle between anterior and posterior series of G1b teeth; H, shell height; L, shell length; Lp, prodissoconch length; p, prodissoconch; pam, posterior adductor muscle; pams, posterior adductor muscle scar; pda, postero-dorsal area; pe periostracum; postG1b, posterior series of G1b teeth; re, resilifer; ri, rim; s, setae; ua, umbonal angle; W, shell width.
FIGURE 12. Philobrya magellanica. A, K in The Genus Philobrya J.G. Cooper, 1867 (Bivalvia: Philobryidae) In Patagonia And Adjacent Antarctic Waters
FIGURE 12. Philobrya magellanica. A, K: syntype (ZMB-Moll 51991), B: specimen from Tierra del Fuego (MACN-In 44454), C‒J, L‒S: specimens from Burdwood Bank (C, J: MACN-In 44460, D, E, G, I: MACN-In 44463, F, H, R, S: MACN-In 44457, L, M, P, Q: MACN-In 44462, N: MACN-In 44459, O: MACN-In 44465). A‒E: outer views right valve (A, B: with periostracum, C‒E: without periostracum), F‒K, M: inner views right valve, L: inner view left valve, N: detail of prodissoconch (slightly tilt), O, Q, R: hinge plates right valve (O: specimen of 4.6 mm L, Q: specimen of 1.7 mm L, R: specimen of 4.3 mm L), P, S: hinge plates left valve (P: specimen of 1.7 mm L, S: specimen of 4.3 mm L). Scale bars A‒M: 1 mm; N: 100 µm; O‒S: 500 µm.
FIGURE 8. Philobrya brattstromi. A‒C, H, I, L‒N in The Genus Philobrya J.G. Cooper, 1867 (Bivalvia: Philobryidae) In Patagonia And Adjacent Antarctic Waters
FIGURE 8. Philobrya brattstromi. A‒C, H, I, L‒N: specimens from Burdwood Bank (A, B, L: MACN-In 44438, C, H, I, M, N: MACN-In 44435), D, F, G, J, K: specimens from Tierra del Fuego (D: MACN-In 44432, F, G: MACN-In 44431, J, K: MLP-Ma 16114), E: holotype (NRM 3894). A‒D, F, J: outer views right valve (A: with periostracum, B‒D, F, J: without periostracum), E, G: outer views left valve (E: with periostracum, G: without periostracum), H: inner view left valve, I: inner view right valve, K: detail of prodissoconch, L, M: hinge plates left valve (L: specimen of 4.9 mm L, M: specimen of 3.3 mm L), N: hinge plate right valve (specimen of 3.2 mm L). Scale bars A‒I: 1 mm; J: 200 µm; K: 100 µm; L‒N: 500 µm.
FIGURE 4. Philobrya atlantica. A in The Genus Philobrya J.G. Cooper, 1867 (Bivalvia: Philobryidae) In Patagonia And Adjacent Antarctic Waters
FIGURE 4. Philobrya atlantica. A: syntype (USNM 97057), B‒K: specimens from Santa Cruz Province (B‒F: MACN-In 44414, G‒K: MACN-In 44415). A‒E: outer views right valve (A‒D: with periostracum, E: without periostracum), F: outer view left valve (without periostracum), G: inner view left valve, H: inner view right valve, I: brooded embryo removed from the demibranch of an adult specimen, J, K: hinge plate of a 4.2 mm L specimen (J: left valve, K: right valve). Scale bars A‒H: 1 mm; I: 100 µm; J‒K: 500 µm.
Subspecies and Distribution. U. a. arctos Linnaeus, 1758 — Europe and W Russia. U. a. alascensis Merriam, 1896 — most of Alaska (excluding Alaska Peninsula, SE panhandle & Kodiak Island group). U. a. beringianus Middendorff, 1853 — NE Russia (Kamchatka Peninsula & N Kuril Islands northward through the Koryak Autonomous District, and along W coast of the Sea of Okhotsk). U. a. collaris Cuvier, 1824 — Russia (Siberia, from E of the Yenisey River to the Bering Sea, but excluding Kamchatka and more southern parts of the Russian Far East), N Mongolia. U. a. dalli Merriam, 1896 — SE Alaska (N of Alexander Archipelago). U. a. gyas Merriam, 1902 — Alaska peninsula. U. a. horribilis Ord, 1815 —W Canada (Yukon, North-West Territories, British Columbia & Alberta), inland W USA (extirpated from S Wyoming to Mexico). U. a. isabellinus Horsfield, 1826 — N India, Pakistan, Afghanistan, N to Kazakhstan and Mongolia (Gobi Desert). U. a. lasiotus Gray, 1867 — Russia (Southern Kuril Islands, Sakhalin, Ussuri/Amur river region of the Russian Far East), NE China, North Korea, and Japan (Hokkaido). U. a. middendorffi Merriam, 1896 — Alaska (Kodiak Island & nearby islands). U. a. pruinosus Blyth, 1853 — Tibetan Plateau, China, N Nepal. U. a. sitkensis Merriam, 1896 — SE Alaska (Alexander Archipelago & adjacent coastal area). U. a. stikeenensis Merriam, 1914 — W Canada (W British Columbia), and formerly W USA (W Washington and Oregon). U. a. syriacus Hemprich & Ehrenberg, 1828 — Middle East, from Turkey to Iran (extirpated in Syria), Caucasus mountains of Russia, Georgia, Armenia and Azerbaijan. in Ursidae
Subspecies and Distribution. U. a. arctos Linnaeus, 1758 — Europe and W Russia. U. a. alascensis Merriam, 1896 — most of Alaska (excluding Alaska Peninsula, SE panhandle & Kodiak Island group). U. a. beringianus Middendorff, 1853 — NE Russia (Kamchatka Peninsula & N Kuril Islands northward through the Koryak Autonomous District, and along W coast of the Sea of Okhotsk). U. a. collaris Cuvier, 1824 — Russia (Siberia, from E of the Yenisey River to the Bering Sea, but excluding Kamchatka and more southern parts of the Russian Far East), N Mongolia. U. a. dalli Merriam, 1896 — SE Alaska (N of Alexander Archipelago). U. a. gyas Merriam, 1902 — Alaska peninsula. U. a. horribilis Ord, 1815 —W Canada (Yukon, North-West Territories, British Columbia & Alberta), inland W USA (extirpated from S Wyoming to Mexico). U. a. isabellinus Horsfield, 1826 — N India, Pakistan, Afghanistan, N to Kazakhstan and Mongolia (Gobi Desert). U. a. lasiotus Gray, 1867 — Russia (Southern Kuril Islands, Sakhalin, Ussuri/Amur river region of the Russian Far East), NE China, North Korea, and Japan (Hokkaido). U. a. middendorffi Merriam, 1896 — Alaska (Kodiak Island & nearby islands). U. a. pruinosus Blyth, 1853 — Tibetan Plateau, China, N Nepal. U. a. sitkensis Merriam, 1896 — SE Alaska (Alexander Archipelago & adjacent coastal area). U. a. stikeenensis Merriam, 1914 — W Canada (W British Columbia), and formerly W USA (W Washington and Oregon). U. a. syriacus Hemprich & Ehrenberg, 1828 — Middle East, from Turkey to Iran (extirpated in Syria), Caucasus mountains of Russia, Georgia, Armenia and Azerbaijan.
Distribution. Throughout mainland SE Asia, from C & S Myanmar to W & SE Thailand, C & S Laos, Cambodia, C & S Vietnam, and Peninsular Malaysia; also present in Borneo, Sumatra, Java, Bali, Lombok, and several adjacent small islands. Most likely extinct from E Bangladesh, where it has not been reported for more than 40 years. Northern and western limits of its range are poorly known. in Manidae
Distribution. Throughout mainland SE Asia, from C & S Myanmar to W & SE Thailand, C & S Laos, Cambodia, C & S Vietnam, and Peninsular Malaysia; also present in Borneo, Sumatra, Java, Bali, Lombok, and several adjacent small islands. Most likely extinct from E Bangladesh, where it has not been reported for more than 40 years. Northern and western limits of its range are poorly known.
Distribution. Sulawesi and adjacent Is (Buton, Kabaena, Muna, Peleng, Lembeh, and on some of the Togian Is); thought to be extinct on Selayar I. Pigs have been widely domesticated through the Indonesian archipelago and beyond. This primarily involved the Eurasian Wild Pig (S. scrofa), but also S. celebensis, the only other species of pig successfully domesticated. Mitochondrial DNA studies of the dispersion of these domesticated forms agree on three major dispersal events, two involving S. scrofa and one S. celebensis. Evidence supports an early human-mediated translocation of S. celebensis to Flores and Timor and two later, separate human-mediated dispersals of domestic pig through islands of SE Asia into Oceania. In addition to Flores and Timor, S. celebensis is also thought to occur in its domesticated form on Halmahera, Lendu, Roti, and Savur Is, and even on Simeulue and Nias Is to the W of Sumatra and far from its island of origin, Sulawesi. In the Moluccas, and possibly elsewhere in this region, introduced S. celebensis are thought to have hybridized with other introduced pigs of S. scrofa derivation, and apparent hybrids between these species are now reported to survive on a number of islands, including Salawatti, Great Kei, Dobu, Seram, Ambon, Bacan, Ternate, Morotai, and New Guinea. It is also reported that in the 19" century the sows of domestic pigs in Sulawesi frequently mated with wild animals, after which they returned to their villages. in Suidae
Distribution. Sulawesi and adjacent Is (Buton, Kabaena, Muna, Peleng, Lembeh, and on some of the Togian Is); thought to be extinct on Selayar I. Pigs have been widely domesticated through the Indonesian archipelago and beyond. This primarily involved the Eurasian Wild Pig (S. scrofa), but also S. celebensis, the only other species of pig successfully domesticated. Mitochondrial DNA studies of the dispersion of these domesticated forms agree on three major dispersal events, two involving S. scrofa and one S. celebensis. Evidence supports an early human-mediated translocation of S. celebensis to Flores and Timor and two later, separate human-mediated dispersals of domestic pig through islands of SE Asia into Oceania. In addition to Flores and Timor, S. celebensis is also thought to occur in its domesticated form on Halmahera, Lendu, Roti, and Savur Is, and even on Simeulue and Nias Is to the W of Sumatra and far from its island of origin, Sulawesi. In the Moluccas, and possibly elsewhere in this region, introduced S. celebensis are thought to have hybridized with other introduced pigs of S. scrofa derivation, and apparent hybrids between these species are now reported to survive on a number of islands, including Salawatti, Great Kei, Dobu, Seram, Ambon, Bacan, Ternate, Morotai, and New Guinea. It is also reported that in the 19" century the sows of domestic pigs in Sulawesi frequently mated with wild animals, after which they returned to their villages.
Distribution. Main tropical rainforest belt from Senegal and Guinea Bissau to NW Uganda and E DR Congo, reaching as S boundary N Angola (Cabinda); no recent records from Gambia or Chad and its presence is uncertain in S Sudan and SW Ethiopia. As a species that may range widely through gallery forests, it may also occur in adjacent countries. in Suidae
Distribution. Main tropical rainforest belt from Senegal and Guinea Bissau to NW Uganda and E DR Congo, reaching as S boundary N Angola (Cabinda); no recent records from Gambia or Chad and its presence is uncertain in S Sudan and SW Ethiopia. As a species that may range widely through gallery forests, it may also occur in adjacent countries.
FIGURE 2. Phlegmariurus aqualupianus—(Colombia: Idrobo & Schultes 994, AAU). A. Growth habit. A1. Close-up of basal and adjacent constricted division. in The Lycopodiaceae of Panamá
FIGURE 2. Phlegmariurus aqualupianus—(Colombia: Idrobo & Schultes 994, AAU). A. Growth habit. A1. Close-up of basal and adjacent constricted division.
Subspecies and Distribution. A. [. fusciceps Gray, 1866 — NW Ecuador, W of the Andes, historically in the provinces of Esmeraldas and Carchi, from the Colombian border S to the Cordillera de Colonche in the Guayas Province (most S record is in "Puente sobre el rio Chimbo," Chimborazo Province), but today it is restricted to two remnant populations (Awa Ethnological Reserve N of the Rio Mira, and Cotacachi-Cayapas Ecological Reserve and adjacent Los Cedros Protected Forest and surrounding forests S of the Rio Mira). A. f. rufiventris Sclater, 1872 — E Panama (Atlantic slope) and W Colombia from the Uraba region in NW Antioquia, N through Cordoba, Sucre, and N Bolivar departments (N distributional limit on the S bank of the Canal del Dique, Cartagena), W of the Rio Cauca to the coast, E to the lower Rio Cauca along the W bank to SC Antioquia (the Cerro Pirre or the Rio Tucuti marks the border with A. geoffroyi grisescens), and S to the Cordillera Occidental of the Andes in SW Colombia (the most southerly record is Barabacoas, Narino Department). in Atelidae
Subspecies and Distribution. A. [. fusciceps Gray, 1866 — NW Ecuador, W of the Andes, historically in the provinces of Esmeraldas and Carchi, from the Colombian border S to the Cordillera de Colonche in the Guayas Province (most S record is in "Puente sobre el rio Chimbo," Chimborazo Province), but today it is restricted to two remnant populations (Awa Ethnological Reserve N of the Rio Mira, and Cotacachi-Cayapas Ecological Reserve and adjacent Los Cedros Protected Forest and surrounding forests S of the Rio Mira). A. f. rufiventris Sclater, 1872 — E Panama (Atlantic slope) and W Colombia from the Uraba region in NW Antioquia, N through Cordoba, Sucre, and N Bolivar departments (N distributional limit on the S bank of the Canal del Dique, Cartagena), W of the Rio Cauca to the coast, E to the lower Rio Cauca along the W bank to SC Antioquia (the Cerro Pirre or the Rio Tucuti marks the border with A. geoffroyi grisescens), and S to the Cordillera Occidental of the Andes in SW Colombia (the most southerly record is Barabacoas, Narino Department).
Supplementary material 1 from: Duran M (2021) An annotated checklist of the amphibians and reptiles of North Padre Island, Texas, USA, with comparisons to adjacent barrier island and mainland herpetofauna. ZooKeys 1073: 119-175. https://doi.org/10.3897/zookeys.1073.57241
Museum and iNaturalist records for Aransas, Cameron, Kenedy, Kleberg, Nueces, San Patricio, and Willacy counties, Texas, and iNaturalist records for North and South Padre and Mustang islands, Texas
Riparian cottonwood trees and adjacent river sediments have different microbial communities and produce methane with contrasting carbon isotope compositions
<p class="Abstract">Rivers and their adjacent riparian forests are intimately linked by the exchange of water, nutrients, and organic matter. Both riparian cottonwood trees and adjacent river sediments host microbial communities including archaeal methanogens, supporting methane production and emission to the atmosphere. Here we combine microbial community and stable isotope analyses to characterize the drivers of methane cycling in distinct anoxic habitats (river sediments versus riparian cottonwood stems) in the Oldman River, southern Alberta (Canada). We demonstrate that, differences in the chemical characteristics of organic matter support divergent microbial communities that generate methane from distinct metabolic pathways. Organic matter in river sediments had C/N ratios approximately 50-fold lower than in tree stems and had more diverse dissolved organic components. Contrasting substrate availability between river sediment and tree stems was likely the primary mechanism for the observed differences in bacterial and methanogen community compositions, and greater microbial diversity in river sediments than in tree stems. The methane carbon isotope composition (δ<sup>13</sup>C values) differed for the tree stem (-103.6 to -70.6‰) and river sediment (-55.1 to -48.4‰) environments, suggesting that methane was primarily produced via CO<sub>2</sub>-reduction in tree stems by Methanobacteriales, while river sediments produced more methane through acetate fermentation primarily by Methanosarcinales. This study demonstrates the importance of organic matter quality and microbial community composition in driving metabolic processes contributing to methane production and emission in rivers and adjacent riparian forests.</p>
Adjacency matrix (.csv) of wood industry project network
<p>Adjacency matrix (.csv) of wood industry project network exported from R code.</p>
Fig. 12 in New records of Hydraenidae and Elmidae (Coleoptera) from Russia and adjacent countries
Fig. 12. General habitus of Stenelmis koreana Satô, 1978 from Khabarovsk Kray, ZMUM. Photo by A. Prokin.
Figs. 9–11 in New records of Hydraenidae and Elmidae (Coleoptera) from Russia and adjacent countries
Figs. 9–11. Habitat of Ochthebius yoshitomii Jäch et Delgado, 2014 on Kunashir Island. Photos by K. Makarov. Arrows indicate actual collecting sites; 1 km SW Alekhino (9–10), S of mouth of Severjanka River (11).
Fig. 8 in New records of Hydraenidae and Elmidae (Coleoptera) from Russia and adjacent countries
Fig. 8. Habitat of O. foveolatus in Samara Oblast'. Arrow indicates actual collecting site. Photo by S. Litovkin).
Fig. 1 in New records of Hydraenidae and Elmidae (Coleoptera) from Russia and adjacent countries
Fig. 1. General habitus of Aulacochthebius narentinus Fig. 2. Habitat of A. narentinus in Samara Oblast' Photo (Reitter, 1885). Photo by S. Litovkin. by S. Litovkin. Arrows indicate actual choriotope.
Fig. 4 in New records of Hydraenidae and Elmidae (Coleoptera) from Russia and adjacent countries
Fig. 4. Habitat of M. paradoxum in Volgograd Oblast', where A. Prokin collected specimens in 2008. Photo by A. Kutuzov.
Subspecies and Distribution. P. c. concolor Linnaeus, 1771 — E Venezuela through the Guianas to lower Amazonian Brazil. P. c. acrocodia Goldman, 1943 — C Brazil (Matto Grosso), SE Bolivia, and the Chaco of Paraguay and Argentina. P. c. anthony: Nelson & Goldman, 1931 — S Venezuela and adjacent N Brazil. P. c. araucanus Osgood, 1943 — S Chile and S Argentina. P.c. azteca Merriam, 1901 — SW USA (Arizona and New Mexico); NW Mexico. P. c. bangsi Merriam, 1901 — Andean Colombia. P. c. borbensis Nelson & Goldman, 1933 — Amazonian Brazil, Colombia, Ecuador, and Peru. P. c. browni Merriam, 1903 — NW Mexico (N Baja California). P. c. cabrerae Pocock, 1940 — NW Argentina. P. c. californica May, 1896 — SW USA (California). P. c. capricornensis Goldman, 1946 — SE Brazil and NE Argentina. P. c. cory: Bangs, 1899 — SE USA (Florida). P. c. costaricensis Merriam, 1901 — Nicaragua through Panama. P. c. cougar Kerr, 1792 — NE USA. P. c. greeni Nelson & Goldman, 1931 — E Brazil. P. c. hippolestes Merriam, 1897 — C USA. P. c. improcera Phillips, 1912 — NW Mexico (S Baja California). P. c. incarum Nelson & Goldman, 1929 — Andean Peru. P.c. kaibabensis Nelson & Goldman, 1931 — W USA (Nevada & Utah). P. c. mayensis Nelson & Goldman, 1929 — S Mexico through El Salvador. P. c. missoulensis Goldman, 1943 — NW Canada through NW USA (Idaho & Montana). P. c. oregonensis Rafinesque, 1832 — NW USA (Oregon and Washington). P. c. osgoodi Nelson & Goldman, 1929 — C Bolivia. P. c. patagonica Merriam, 1901 — S Argentina (E side of Lago Pueyrredon). P. c. pearsoni Thomas, 1901 — Patagonian Argentina and Chile. P. c. puma Molina, 1782 — C Chile and adjacent Argentina. P. c. schorgeri Jackson, 1955 — Midwestern USA P. c. soderstromi Lonnberg, 1913 — Andean Ecuador. P. c. stanleyana Goldman, 1936 — S USA (Texas) and adjacent Mexico. P. c. vancouverensis Nelson & Goldman, 1932 — SW Canada (Vancouver I). in Felidae
Subspecies and Distribution. P. c. concolor Linnaeus, 1771 — E Venezuela through the Guianas to lower Amazonian Brazil. P. c. acrocodia Goldman, 1943 — C Brazil (Matto Grosso), SE Bolivia, and the Chaco of Paraguay and Argentina. P. c. anthony: Nelson & Goldman, 1931 — S Venezuela and adjacent N Brazil. P. c. araucanus Osgood, 1943 — S Chile and S Argentina. P.c. azteca Merriam, 1901 — SW USA (Arizona and New Mexico); NW Mexico. P. c. bangsi Merriam, 1901 — Andean Colombia. P. c. borbensis Nelson & Goldman, 1933 — Amazonian Brazil, Colombia, Ecuador, and Peru. P. c. browni Merriam, 1903 — NW Mexico (N Baja California). P. c. cabrerae Pocock, 1940 — NW Argentina. P. c. californica May, 1896 — SW USA (California). P. c. capricornensis Goldman, 1946 — SE Brazil and NE Argentina. P. c. cory: Bangs, 1899 — SE USA (Florida). P. c. costaricensis Merriam, 1901 — Nicaragua through Panama. P. c. cougar Kerr, 1792 — NE USA. P. c. greeni Nelson & Goldman, 1931 — E Brazil. P. c. hippolestes Merriam, 1897 — C USA. P. c. improcera Phillips, 1912 — NW Mexico (S Baja California). P. c. incarum Nelson & Goldman, 1929 — Andean Peru. P.c. kaibabensis Nelson & Goldman, 1931 — W USA (Nevada & Utah). P. c. mayensis Nelson & Goldman, 1929 — S Mexico through El Salvador. P. c. missoulensis Goldman, 1943 — NW Canada through NW USA (Idaho & Montana). P. c. oregonensis Rafinesque, 1832 — NW USA (Oregon and Washington). P. c. osgoodi Nelson & Goldman, 1929 — C Bolivia. P. c. patagonica Merriam, 1901 — S Argentina (E side of Lago Pueyrredon). P. c. pearsoni Thomas, 1901 — Patagonian Argentina and Chile. P. c. puma Molina, 1782 — C Chile and adjacent Argentina. P. c. schorgeri Jackson, 1955 — Midwestern USA P. c. soderstromi Lonnberg, 1913 — Andean Ecuador. P. c. stanleyana Goldman, 1936 — S USA (Texas) and adjacent Mexico. P. c. vancouverensis Nelson & Goldman, 1932 — SW Canada (Vancouver I).
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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.