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Fig. 11 in Drymini of Madagascar, with description of a new genus and three new species (Hemiptera: Heteroptera: Rhyparochromidae)
Fig. 11. Dorsal view of Appolonius madagascariensis Zámbó & Kondorosy, sp. nov. (Photo by A. Zámbó).
Figs 3–10 in Drymini of Madagascar, with description of a new genus and three new species (Hemiptera: Heteroptera: Rhyparochromidae)
Figs 3–10. Male genitalia of Malgadrymus and Appolonius species. 3–4 – Malgadrymus bimaculatus Zámbó & Kondorosy, sp. nov. (3 – pygophore, dorsal view; 4 – same, caudodorsal view); 5 – Pygophore of M. pameroides Zámbó & Kondorosy, sp. nov. (dorsal view); 6 – Pygophore of Appolonius madagascariensis Zámbó & Kondorosy, sp. nov. (dorsal view); 7–8 – Left paramere of Malgadrymus bimaculatus Zámbó & Kondorosy, sp. nov. (different views); 9 – Left paramere of Malgadrymus pameroides Zámbó & Kondorosy, sp. nov. (ventral view); 10 – Paramere of Appolonius madagascariensis Zámbó & Kondorosy, sp. nov. (ventral view). (Drawings by Sz. Kovács).
Figs 1–2 in Drymini of Madagascar, with description of a new genus and three new species (Hemiptera: Heteroptera: Rhyparochromidae)
Figs 1–2. Dorsal view of Malgadrymus species.1 – M. pameroides Zámbó & Kondorosy, sp. nov.; 2 – M. bimaculatus Zámbó & Kondorosy, sp. nov. (Photos by Csaba Pintér).
Multiplexed and scalable cellular phenotyping toward the standardized three-dimensional human neuropathology
<p>The dataset for the publication. Cite the publication if you use the datasets.</p>
Figures Į–Į0. Marimatha adults. Į M. nigrofimbria ♂, 1.4 mi WSW Anthony, Marion Co., Florida 2 M. nigrofimbria ♀, Big Cypress Natute Preserve, Collier Co., Florida 3 M. squala ♂, Madera Canyon 4880', Santa Rita Mts., Santa Cruz Co., Arizona 4 M. squala ♀, Madera Canyon 4880', Santa Rita Mts., Santa Cruz Co., Arizona 5 M. quadrata ♂, Madera Canyon 3800', Santa Rita Mts., Pima Co., Arizona 6 M. quadrata ♀, Concan, Uvalde Co., Texas 7 M. tripuncta ♂, Fuchs Hammock near Homestead, Dade Co., Florida 8 M. tripuncta ♀, Fuchs Hammock near Homestead, Dade Co., Florida 9 M. piscimala ♂, Brown Canyon, Baboquivari Mts., Pima Co., Arizona Į0 M. piscimala ♀, Mission, Hidalgo Co., Texas. in Review of the North American species of Marimatha Walker with descriptions of three new species (Lepidoptera, Noctuidae, Eustrotiinae) and the description of Pseudomarimatha flava (Noctuinae, Elaphriini), a new genus and species confused with Marimatha
Figures Į–Į0. Marimatha adults. Į M. nigrofimbria ♂, 1.4 mi WSW Anthony, Marion Co., Florida 2 M. nigrofimbria ♀, Big Cypress Natute Preserve, Collier Co., Florida 3 M. squala ♂, Madera Canyon 4880', Santa Rita Mts., Santa Cruz Co., Arizona 4 M. squala ♀, Madera Canyon 4880', Santa Rita Mts., Santa Cruz Co., Arizona 5 M. quadrata ♂, Madera Canyon 3800', Santa Rita Mts., Pima Co., Arizona 6 M. quadrata ♀, Concan, Uvalde Co., Texas 7 M. tripuncta ♂, Fuchs Hammock near Homestead, Dade Co., Florida 8 M. tripuncta ♀, Fuchs Hammock near Homestead, Dade Co., Florida 9 M. piscimala ♂, Brown Canyon, Baboquivari Mts., Pima Co., Arizona Į0 M. piscimala ♀, Mission, Hidalgo Co., Texas.
Figures 23–26. Pseudomarimatha flava adults and genitalia. 23 in Review of the North American species of Marimatha Walker with descriptions of three new species (Lepidoptera, Noctuidae, Eustrotiinae) and the description of Pseudomarimatha flava (Noctuinae, Elaphriini), a new genus and species confused with Marimatha
Figures 23–26. Pseudomarimatha flava adults and genitalia. 23 ♂, Portal, Cochise Co, Arizona 24 ♀, Onion Saddle, Chiricahua Mts, Cochise Co., Arizona 25 male genitalia 26 female genitalia.
Dataset for "Three-dimensional modeling of the ground electric field in Fennoscandia during the Halloween geomagnetic storm", Marshalko et al. (2023), Space Weather
<p>Results of 3-D modeling of the ground electric field in Fennoscandia during the Halloween geomagnetic storm in 2003 (29-31 October).</p> <p>Electric_field_YYYYMMDDHHMMSS_YYYYMMDDHHMMSS.h5 files (in hdf5 format) contain horizontal electric field components Ex and Ey (in mV/km) corresponding to 6 h of data and latitude and longitude grids corresponding to Ex and Ey arrays. Ex and Ey are 2160x567x543 arrays (temporal resolution is 10 s, thus, 2160 time steps). Latitude and Longitude are 567x543 arrays. All values are in single-precision floating-point format. Electric field values were obtained with the use of the conductivity-based inducing source following Marshalko et al. (2023).</p> <p>Files Electric_field_CB_20031029000000_20031031235950.dat, Electric_field_MT_20031029000000_20031031235950.dat, and Electric_field_SECS_20031029000000_20031031235950.dat contain the ground electric field time series (in mV/km) modeled during the Halloween geomagnetic storm in 2003 (29-31 October) at IMAGE magnetometers' locations, Mäntsälä Finnish natural gas pipeline GIC recording point (MAN), and Point X located 0.5 degrees north of MAN. The files are in plain-text (column-based) format. Electric field values in Electric_field_CB_20031029000000_20031031235950.dat, Electric_field_MT_20031029000000_20031031235950.dat, and Electric_field_SECS_20031029000000_20031031235950.dat were obtained with the use of the conductivity-based inducing source, MT intersite impedance method, and Spherical Elementary Current Systems (SECS) based approach, correspondingly, following Marshalko et al. (2023).</p>
Floristic composition in three different forest types in western Amazonia
<p><span><span>Aim</span></span><span>: The latitudinal gradient is considered a first-order biogeographical pattern for most taxonomic groups. Yet, latitudinal changes in plant ecological communities are not always consistent, and this could be related to the physical and biological characteristics of different forest types. In this study, we compare latitudinal changes in floristic diversity (alpha diversity), composition (beta diversity), and dominance across different tropical forest types: floodplain, <em>terra</em> <em>firme</em>, and submontane forests. </span></p> <p><span><span>Location</span></span><span>: Western Amazonia (Ecuador, Peru, and Bolivia).</span></p> <p><span><span>Taxon</span>: Woody plants. </span></p> <p><span><span>Methods</span></span><span>: We inventoried 1,978 species and 31,203 individuals of vascular plants with a diameter at breast height ≥ 2.5 cm in 118 0.1-ha plots over a 1,800-km latitudinal gradient in three different forest types. The relationships between alpha diversity, latitude, and forest type were analysed using generalised linear mixed models (GLMMs). Semi-parametric permutational multivariate analysis of variance was used to investigate the effects of latitude and forest type on beta diversity. Dominant species abundances were correlated with non-metric multidimensional scaling ordination axes to reflect their contributions in shaping changes in beta diversity. </span></p> <p><span><span>Results</span></span><span>: Alpha diversity increased towards equatorial latitudes in <em>terra</em> <em>firme</em> and submontane forests but remained relatively constant in floodplains. Beta diversity of all forest types changed with latitude, although less clearly in floodplains. Overall, the abundances of dominant species decreased towards the Equator, though in floodplains they were more homogeneous along the gradient.</span></p> <p><span><span>Main conclusions</span></span><span>: Alpha diversity, beta diversity and dominance patterns differed across forest types. In floodplain forests, the flooding regime is a strong predictor of floristic composition, which maintains alpha diversity constant along the latitudinal gradient. However, alpha and beta diversity in unflooded forests increase steadily towards equatorial latitudes. Furthermore, we found fewer dominant species contributing to changes beta diversity in floodplain forests. Shifts in abundance of dominant species over gradients can explain how beta diversity is driven differently per forest type.</span></p>
Figs 1–5 in One new genus and three new species of wingless grasshoppers from Xizang, China (Orthoptera: Acridoidea)
Figs 1–5. Pseudozubovskia xizangensis sp. nov. 1. Body. 2. Head and pronotum. 3–5. Terminalia. 3–4. ♂. 5. ♀. 1, 4. Lateral view. 2–3, 5. Dorsal view. Scare bar = 1 mm.
Figs 6–11 in One new genus and three new species of wingless grasshoppers from Xizang, China (Orthoptera: Acridoidea)
Figs 6–11. Eokingdonella gongbugyanda sp. nov. 6. Body. 7. ♂, terminalia. 8. Head and pronotum. 9–11. ♀, terminalia. 6, 10. Lateral view. 7–8, 11. Dorsal view. 9. Ventral view. Scare bar = 1 mm.
Figs 12–15 in One new genus and three new species of wingless grasshoppers from Xizang, China (Orthoptera: Acridoidea)
Figs 12–15. Dysanema magna sp. nov. 12. Body. 13. Head and pronotum. 14–15. ♀, terminalia. 12. Lateral view. 13–14. Dorsal view. 15. Ventral view. Scare bar = 1 mm.
Text-fig. 41. Scanning electron microscope (SEM) images of "Pollen clump with tricolpate pollen sp. 5"; Catefica locality, Portugal. a) Pollen clump, probably coprolite but containing one kind of pollen; b, c) Pollen grains from pollen clump in oblique equatorial view (b) and polar view (c) showing the three apertures with a distinct aperture margin and the coarse reticulum; d) Detail of wall of a broken pollen grain showing long straight columellae and a thin foot layer. Specimen, Catefica 50-S115858 (a–d). Scale bars = 600 Μm (a), 6 Μm (b, c), 1.5 Μm (d). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 41. Scanning electron microscope (SEM) images of "Pollen clump with tricolpate pollen sp. 5"; Catefica locality, Portugal. a) Pollen clump, probably coprolite but containing one kind of pollen; b, c) Pollen grains from pollen clump in oblique equatorial view (b) and polar view (c) showing the three apertures with a distinct aperture margin and the coarse reticulum; d) Detail of wall of a broken pollen grain showing long straight columellae and a thin foot layer. Specimen, Catefica 50-S115858 (a–d). Scale bars = 600 Μm (a), 6 Μm (b, c), 1.5 Μm (d).
Text-fig. 42. Scanning electron microscope (SEM, a, b, e) and synchrotron radiation X-ray tomographic microscopy (SRXTM, c, d, f–g) images of "Tricarpellate flower sp. 1"; Catefica locality, Portugal. a, b) Flower bud in two different lateral views showing semiinferior ovary and perianth; c) Longitudinal section (orthoslice yz0340) through flower bud in (a and b) showing the semi-inferior gynoecium and perigynous insertion of other floral parts; d) Volume rendering of flower bud with pedicel preserved; note the depression/split in one of the corner apparently separating two perianth lobes of the outer perianth whorl (t-o) and exposing one tepal of the inner whorl (t-i); e) Flower bud with pedicel preserved; note broad tepals of the outer whorl (t-o) and tepal of the inner whorl abraded exposing a broad stamen (st); f, g) Transverse sections through flower bud in (a and b) at two different levels above the insertion of the perianth (f, rec-file 1310; g, xy0280) showing the trimerous organization of the flower and the free, laterally flattened carpels; yellow indicates the two whorls of the androecium, each with three stamens. Specimens, Catefica 50-S171520 (a–c, f), Catefica 50-S174902 (d), Catefica MM154-P0271 (e), Catefica 49-S175354 (g). Scale bars = 300 Μm (a–e). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 42. Scanning electron microscope (SEM, a, b, e) and synchrotron radiation X-ray tomographic microscopy (SRXTM, c, d, f–g) images of "Tricarpellate flower sp. 1"; Catefica locality, Portugal. a, b) Flower bud in two different lateral views showing semiinferior ovary and perianth; c) Longitudinal section (orthoslice yz0340) through flower bud in (a and b) showing the semi-inferior gynoecium and perigynous insertion of other floral parts; d) Volume rendering of flower bud with pedicel preserved; note the depression/split in one of the corner apparently separating two perianth lobes of the outer perianth whorl (t-o) and exposing one tepal of the inner whorl (t-i); e) Flower bud with pedicel preserved; note broad tepals of the outer whorl (t-o) and tepal of the inner whorl abraded exposing a broad stamen (st); f, g) Transverse sections through flower bud in (a and b) at two different levels above the insertion of the perianth (f, rec-file 1310; g, xy0280) showing the trimerous organization of the flower and the free, laterally flattened carpels; yellow indicates the two whorls of the androecium, each with three stamens. Specimens, Catefica 50-S171520 (a–c, f), Catefica 50-S174902 (d), Catefica MM154-P0271 (e), Catefica 49-S175354 (g). Scale bars = 300 Μm (a–e).
Text-fig. 17. Scanning electron microscope (SEM) images of fruits of Serialis communis (a) and Serialis crassitesta (b); Catefica locality, Portugal. a) Oblique lateral view of fruit showing three laterally coherent seeds from which the fruit wall has been almost completely lost showing the prominent micropylar region; b) Oblique lateral view of fruit containing three or four laterally coherent seeds with their micropylar regions oriented to the left. Specimens, Catefica MM92-P0167 (a), Catefica MM92-P0169 (b). Scale bars = 300 Μm (a, b). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 17. Scanning electron microscope (SEM) images of fruits of Serialis communis (a) and Serialis crassitesta (b); Catefica locality, Portugal. a) Oblique lateral view of fruit showing three laterally coherent seeds from which the fruit wall has been almost completely lost showing the prominent micropylar region; b) Oblique lateral view of fruit containing three or four laterally coherent seeds with their micropylar regions oriented to the left. Specimens, Catefica MM92-P0167 (a), Catefica MM92-P0169 (b). Scale bars = 300 Μm (a, b).
Text-fig. 22. Scanning electron microscope (SEM, a–c) and synchrotron radiation X-ray tomographic microscopy (SRXTM, d) images of Ibericarpus cuneiformis gen. et sp. nov.; Catefica locality, Portugal. a) Fruiting axis bearing an elongated receptacle with numerous diamond-shaped scars from detached fruitlets; note the absence of scars from bracts, tepals or stamens at the transition to the fruitlet scars and the stalk (arrow); b) Group of ten fruitlets detached from fruiting axis in (a) showing apical stigmatic region and distinctive bulging isodiametric epidermal cells; c) Detached fruitlet showing apical stigmatic region; d) Volume rendering of three adhering fruits showing apical stigmatic region and distinctive bulging isodiametric epidermal cells. Specimens, Catefica MM75-P0477 (a, b), Catefica 49-S115852 (c), Catefica 50-S174907 (d). Scale bars = 300 Μm (a–d). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 22. Scanning electron microscope (SEM, a–c) and synchrotron radiation X-ray tomographic microscopy (SRXTM, d) images of Ibericarpus cuneiformis gen. et sp. nov.; Catefica locality, Portugal. a) Fruiting axis bearing an elongated receptacle with numerous diamond-shaped scars from detached fruitlets; note the absence of scars from bracts, tepals or stamens at the transition to the fruitlet scars and the stalk (arrow); b) Group of ten fruitlets detached from fruiting axis in (a) showing apical stigmatic region and distinctive bulging isodiametric epidermal cells; c) Detached fruitlet showing apical stigmatic region; d) Volume rendering of three adhering fruits showing apical stigmatic region and distinctive bulging isodiametric epidermal cells. Specimens, Catefica MM75-P0477 (a, b), Catefica 49-S115852 (c), Catefica 50-S174907 (d). Scale bars = 300 Μm (a–d).
Text-fig. 33. Synchrotron radiation X-ray tomographic microscopy (SRXTM, a, c) and scanning electron microscope (SEM, b, d) images of Paisia pantoporata (a–c) and?Paisia sp. (d); Catefica locality, Portugal. a) Lateral view (volume rendering) of flower showing the carpels (c) and the fleshy tepals (t) that have a slightly bulge near the base; b) Pollen grains in situ from stamen showing scattered pores and spiny supratectal ornamentation; c) Transverse section (orthoslice xz1024) through flower showing the pentamerous organization with five tepals (green) five stamens (yellow) and five carpels (red) all on the same radii; d) Lateral view of floral structure with three free carpels borne on the swollen receptacle that has poorly defined facets at the apex indicating the former presence of perianth parts. Specimens, Catefica 49-S101214 (a, c), Catefica 50-S170188 (b), Catefica MM125-P0292 (d). Scale bars = 300 Μm (a, c, d), 6 Μm (b). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 33. Synchrotron radiation X-ray tomographic microscopy (SRXTM, a, c) and scanning electron microscope (SEM, b, d) images of Paisia pantoporata (a–c) and?Paisia sp. (d); Catefica locality, Portugal. a) Lateral view (volume rendering) of flower showing the carpels (c) and the fleshy tepals (t) that have a slightly bulge near the base; b) Pollen grains in situ from stamen showing scattered pores and spiny supratectal ornamentation; c) Transverse section (orthoslice xz1024) through flower showing the pentamerous organization with five tepals (green) five stamens (yellow) and five carpels (red) all on the same radii; d) Lateral view of floral structure with three free carpels borne on the swollen receptacle that has poorly defined facets at the apex indicating the former presence of perianth parts. Specimens, Catefica 49-S101214 (a, c), Catefica 50-S170188 (b), Catefica MM125-P0292 (d). Scale bars = 300 Μm (a, c, d), 6 Μm (b).
Text-fig. 2. Scanning electron microscope (SEM, a, c–f) and synchrotron radiation X-ray tomographic microscopy (SRXTM, b, g) images of the flower of Mugideiriflora portugallica (a, b) and fruits, seeds and pollen of Canrightia resinifera (c–g); Catefica locality, Portugal. a) Oblique, apical view of flower showing multiparted organization with numerous laminar tepals, stamens that are rhomboidal and flattened in transverse section and carpels that are borne on the short conical apex of the receptacle; b) Transverse section (orthoslice xy0800) through basal part of flower showing the elongate bases of the laminar tepals and the flattened rhomboidal bases of the stamens; c) Fruit in lateral view showing irregular surface resulting from the abundant resin bodies in the fruit and hypanthium wall, scars from stamens on the rim of the hypanthium (arrowheads) and the lobed apical stigmatic region (st); d) Broken fruit with one or two seeds missing but showing three pendant, orthotropous seeds with pointed micropylar regions (mi) and a finely pitted crystalliferous endotesta; note the remains of the apical vascular bundles (vb); e) Single seed isolated from a fruit showing two distinct bundles (vb) still attached apically to the chalazal region of the seed, the pointed micropyle (mi) and the finely pitted surface of the crystalliferous endotesta; f) Monocolpate pollen from stigmatic region of fruit showing the long colpus and coarse reticulum; g) Transverse section (orthoslice xy0705) through a fruit showing four seeds all with radially elongated endothelium cells formed from the inner epidermis of the tegmen (asterisks). Specimens, Catefica 150-S174254 (a, b), Catefica 49-S170377 (c), Catefica 49-S170372 (d), Catefica 50-S170401 (e), Catefica 50-S170404 (f), Catefica 50-S174906 (g). Scale bars = 300 Μm (a–e, g), 6 Μm (f). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 2. Scanning electron microscope (SEM, a, c–f) and synchrotron radiation X-ray tomographic microscopy (SRXTM, b, g) images of the flower of Mugideiriflora portugallica (a, b) and fruits, seeds and pollen of Canrightia resinifera (c–g); Catefica locality, Portugal. a) Oblique, apical view of flower showing multiparted organization with numerous laminar tepals, stamens that are rhomboidal and flattened in transverse section and carpels that are borne on the short conical apex of the receptacle; b) Transverse section (orthoslice xy0800) through basal part of flower showing the elongate bases of the laminar tepals and the flattened rhomboidal bases of the stamens; c) Fruit in lateral view showing irregular surface resulting from the abundant resin bodies in the fruit and hypanthium wall, scars from stamens on the rim of the hypanthium (arrowheads) and the lobed apical stigmatic region (st); d) Broken fruit with one or two seeds missing but showing three pendant, orthotropous seeds with pointed micropylar regions (mi) and a finely pitted crystalliferous endotesta; note the remains of the apical vascular bundles (vb); e) Single seed isolated from a fruit showing two distinct bundles (vb) still attached apically to the chalazal region of the seed, the pointed micropyle (mi) and the finely pitted surface of the crystalliferous endotesta; f) Monocolpate pollen from stigmatic region of fruit showing the long colpus and coarse reticulum; g) Transverse section (orthoslice xy0705) through a fruit showing four seeds all with radially elongated endothelium cells formed from the inner epidermis of the tegmen (asterisks). Specimens, Catefica 150-S174254 (a, b), Catefica 49-S170377 (c), Catefica 49-S170372 (d), Catefica 50-S170401 (e), Catefica 50-S170404 (f), Catefica 50-S174906 (g). Scale bars = 300 Μm (a–e, g), 6 Μm (f).
Fig. 16 in Three new deep-sea species of Thyasiridae (Mollusca: Bivalvia) from the northwestern Pacific Ocean
Fig. 16. Thyasira kharkovensis sp. nov. A. Gross anatomy after removal of right valve and mantle, shell length 5.2 mm (MIMB 43830). B. Labial palps (MIMB 43830). C. Bulbous portion of foot (MIMB 43830). D. Gross anatomy after further removal of right ctenidium (MIMB 43830). E–F. Gross anatomy after further removal of right lateral body pouch (MIMB 43830). G–H. Digestive system, shell length 4.5 mm (MIMB 43826). Abbreviations: see Material and methods. Scale bars: A, D–E= 1 mm; B–C, F–H = 500 µm.
Fig. 13 in Three new deep-sea species of Thyasiridae (Mollusca: Bivalvia) from the northwestern Pacific Ocean
Fig. 13. Thyasira kharkovensis sp. nov. A–E. Paratype (MIMB 43825), exterior of right valve and dorsal views of both valves, shell length 5.5 mm. D. Lunule. E. Escutcheon with auricle. F. Paratype (MIMB 43825), shell length 5.2 mm. G–H. Variability of shell shape. G. Shell length 3.3 mm (MIMB 43835). H. Shell length 2.3 mm (MIMB 43832). Scale bars = 1 mm.
Fig. 10 in Three new deep-sea species of Thyasiridae (Mollusca: Bivalvia) from the northwestern Pacific Ocean
Fig. 10. Scanning electron micrographs of Parathyasira pauli sp. nov. (IORAS OBF collection Cat. BIV00041). A–B. Dorsal and oblique dorsal views of both valves. C. Lunule. D. Escutcheon. E. Prodissoconchs. F. Interior view of left valve of young specimen, shell length 1.3 mm. G–H. Prodissoconchs of different specimens. Scale bars = 100 µm.
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.