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.
22
datasets available to search
ShareScore release 0.9.0
Dataset results
22 results for “black color”
- Fore wing with areolet open (a); body and wings colorations variable but usually wings hyaline and body yellow interspersed with black markings (b) …………………………………2 (Epirhyssa) 2. Face smooth to sparsely punctate (A-B), without transverse rugosities ……………………………3 - Face transversely rugulose punctate or transversely striate (a-b) ……………………………………5 in A review of the Afrotropical Rhyssinae (Hymenoptera: Ichneumonidae) with the descriptions of five new species
- Fore wing with areolet open (a); body and wings colorations variable but usually wings hyaline and body yellow interspersed with black markings (b) …………………………………2 (Epirhyssa) 2. Face smooth to sparsely punctate (A-B), without transverse rugosities ……………………………3 - Face transversely rugulose punctate or transversely striate (a-b) ……………………………………5
- Sternite 1 without a pair of submedian tubercles, tubercles present on sternites 2–4 only (a); general coloration pale to striking yellow with isolated black markings (b) …………………………………7 7. Apex of subtegular ridge concave, laterally flanged (A) ……………………………………………8 - Apex of subtegular ridge convex, without lateral flange (a) ……………………………………9 in A review of the Afrotropical Rhyssinae (Hymenoptera: Ichneumonidae) with the descriptions of five new species
- Sternite 1 without a pair of submedian tubercles, tubercles present on sternites 2–4 only (a); general coloration pale to striking yellow with isolated black markings (b) …………………………………7 7. Apex of subtegular ridge concave, laterally flanged (A) ……………………………………………8 - Apex of subtegular ridge convex, without lateral flange (a) ……………………………………9
Black and orange coloration predict success during male-male competition in the guppy
<p>Investigating how both intrasexual competition and intersexual mate choice act within a single system is crucial to understanding the maintenance and diversity of sexually-dimorphic traits. These two processes can act in concert by selecting for the same trait, or in opposition by selecting for different extremes of the same trait; they can also act on different traits, potentially increasing overall trait complexity. We asked whether male-male competition and female mate choice act on the same male traits using Trinidadian guppies, which exhibit complex male-limited color patterns and sexual size dimorphism. We used behavioral assays to assess the relationship between color and male competitive success and then compared our results to the plethora of data on female choice and male color in our study population. We found that males initiated more contests if they were larger than their competitor. Males won contests more often if they had more black coloration than their competitor, and the effect of black was stronger when the male had less orange than his competitor. Additionally, males won more often if they had either more structural color (iridescence) and more orange, or less structural color and less orange than their competitor, suggesting multiple combinations of color traits predict success. Females from our study population exhibit strong preferences for orange coloration. Thus, traits favored in male contests differ from those favored by intersexual selection in this population. Our results suggest that mate choice and male-male competition together promote increased color pattern complexity in this species.</p>
Text-fig. 6. Stratigraphic and phylogenetic placement inferred for fossil Fraxinus fruits. Only Fraxinus fossil fruits identified on the section level are included. The black color represents selected fossil fruits from published literature (excluding some Eocene North American occurrences not assigned to section), the red color represents the fossil fruits from the Lühe flora, Yunnan, Southwest China. The phylogenetic relationships are based on Hinsinger et al. (2013). in Fraxinus L. (Oleaceae) Fruits From The Early Oligocene Of Southwest China And Their Biogeographic Implications
Text-fig. 6. Stratigraphic and phylogenetic placement inferred for fossil Fraxinus fruits. Only Fraxinus fossil fruits identified on the section level are included. The black color represents selected fossil fruits from published literature (excluding some Eocene North American occurrences not assigned to section), the red color represents the fossil fruits from the Lühe flora, Yunnan, Southwest China. The phylogenetic relationships are based on Hinsinger et al. (2013).
Рис. 3. Схема миграций виΑов рыб, участвующих в современной Αинамике ихтиофауны на территории НТТ: 1 — разΛивы; 2 — намывы. Черным цветом обозначены направΛения миграций из реки Туманной; красным — из оз. Хасан и РазΛивов; синим — с мест зимовки в реках южного Приморья; зеΛеным — сезонные миграции из южных морей Fig. 3. Scheme of migration of fish species involved in the modern dynamics of ichthyofauna on the territory of LRT: 1 — spills; 2 — alluvial. Black color indicates the direction of migration from the Tumannaya river; red — from lake Khasan and spills; blue — from wintering places in the rivers of southern Primorye; green — seasonal migration from the south seas in Transboundary Migration And The Local Constraints In The Dynamic Of Fish Fauna In The Lower Reaches Of Tumannaya River
Рис. 3. Схема миграций виΑов рыб, участвующих в современной Αинамике ихтиофауны на территории НТТ: 1 — разΛивы; 2 — намывы. Черным цветом обозначены направΛения миграций из реки Туманной; красным — из оз. Хасан и РазΛивов; синим — с мест зимовки в реках южного Приморья; зеΛеным — сезонные миграции из южных морей Fig. 3. Scheme of migration of fish species involved in the modern dynamics of ichthyofauna on the territory of LRT: 1 — spills; 2 — alluvial. Black color indicates the direction of migration from the Tumannaya river; red — from lake Khasan and spills; blue — from wintering places in the rivers of southern Primorye; green — seasonal migration from the south seas
"I'm something of an untrained, unofficial cultural anthropologist myself. Ihave a business interviewing people to capture their personal histories. I'm always interested how people fit into their world and how they affect their world. I'm a graphic designer who works in the same building as the printing presses that I recorded. Iwalk past the presses every day on my way to talk to the folks in the prepress department. I'm on friendly but not drinking terms with the pressmen. I'm a friend with the prepress manager. Three Heidelberg presses are installed side by side in an open warehouse-like room. The presses are about twenty feet long and about five feet high. With their series of four humps or mounds where each printing cylinder is located, the presses remind one of giant, gray, mechanical caterpillars. Each press has a cyan cylinder, a magenta cylinder, a yellow cylinder and a black cylinder – so the humps are brightly colored. The presses are well lit by banks of fluorescent lights hanging from the ceiling over each press. When you walk into the press room you hear the sound of rock music blaring from a boom box radio mixed with the general din of the presses. It is only when you walk up to a press like Idid for the recordings that you really start to hear the individual strains of clicking, clacking and mechanical, syncopated chattering. When I made my recordings I was intrigued by the subtle variations in the sounds produced by these machines that aren't apparent when you first walk through the door. The pressmen were kind enough to allow me to walk right up to the presses and poke my microphone quite close to the rotating press cylinders. Iuse a Danish Pro Audio microphone about the size of a pencil eraser. An extremely sensitive mic with the capacity for capturing loud sounds such as the presses up close. Rotating the mic to one side or the other focused on the unique sounds coming from one cylinder or the other." [Kevin/KMerrell]18 in Collecting Sounds. Online Sharing of Field Recordings as Cultural Practice
"I'm something of an untrained, unofficial cultural anthropologist myself. Ihave a business interviewing people to capture their personal histories. I'm always interested how people fit into their world and how they affect their world. I'm a graphic designer who works in the same building as the printing presses that I recorded. Iwalk past the presses every day on my way to talk to the folks in the prepress department. I'm on friendly but not drinking terms with the pressmen. I'm a friend with the prepress manager. Three Heidelberg presses are installed side by side in an open warehouse-like room. The presses are about twenty feet long and about five feet high. With their series of four humps or mounds where each printing cylinder is located, the presses remind one of giant, gray, mechanical caterpillars. Each press has a cyan cylinder, a magenta cylinder, a yellow cylinder and a black cylinder – so the humps are brightly colored. The presses are well lit by banks of fluorescent lights hanging from the ceiling over each press. When you walk into the press room you hear the sound of rock music blaring from a boom box radio mixed with the general din of the presses. It is only when you walk up to a press like Idid for the recordings that you really start to hear the individual strains of clicking, clacking and mechanical, syncopated chattering. When I made my recordings I was intrigued by the subtle variations in the sounds produced by these machines that aren't apparent when you first walk through the door. The pressmen were kind enough to allow me to walk right up to the presses and poke my microphone quite close to the rotating press cylinders. Iuse a Danish Pro Audio microphone about the size of a pencil eraser. An extremely sensitive mic with the capacity for capturing loud sounds such as the presses up close. Rotating the mic to one side or the other focused on the unique sounds coming from one cylinder or the other." [Kevin/KMerrell]18
Black and orange coloration predict success during male-male competition in the guppy
Open the record for dataset details and reuse information.
Hidden white and black feather layers enhance plumage coloration in tanagers and other songbirds
Open the record for dataset details and reuse information.
Data from: Not everything is black and white: color and behavioral variation reveal a continuum between cryptic and aposematic strategies in a polymorphic poison frog
Aposematism and crypsis are often viewed as two extremes of a continuum of visual conspicuousness to predators. Theory predicts that behavioral and coloration conspicuousness should vary in tandem along the conspicuousness spectrum for antipredator strategies to be effective. Here we used visual modeling of contrast and behavioral observations to examine the conspicuousness of four populations of the granular poison frog, Oophaga granulifera, which exhibits almost continuous variation in dorsal color. The patterns of geographic variation in color, visual contrast, and behavior support a gradient of overall conspicuousness along the distribution of O. granulifera. Red and green populations, at the extremes of the color distribution, differ in all elements of color, contrast, and behavior, strongly reflecting aposematic and cryptic strategies. However, there is no smooth cline in any elements of behavior or coloration between the two extremes. Instead populations of intermediate colors attain intermediate conspicuousness by displaying different combinations of aposematic and cryptic traits. We argue that coloration divergence among populations may be linked to the evolution of a gradient of strategies to balance the costs of detection by predators and the benefits of learned aversion.
Distribution. Angola, DR Congo, Malawi, Mozambique, Tanzania, and Zambia. Description. Head-body 46:5-47-8 cm (males), 44-45-5 cm (females), tail 40-43 cm (males), 38-39 cm (females), hindfoot 8:7-9-8 cm (males), 8-9 cm (females), ear 4-7-5-4 cm (males), 5-1-5-8 cm (females); weight 1-3-2 kg. The coat color is pale ocher, with brownish or grayish tones; melanistic individuals are quite common. The throat and chest are blackish, and the ventral pelage varies from creamy white to dirty white. The stripes and spots on the body vary from different hues of brown to black. The nuchal stripes run as two parallel lines from the nape to the shoulders, where they diverge and enlarge towards the elbows; they are not so conspicuously marked as in other genet species. Below them, a pair of thinner stripes and small spots are scattered on the shoulders and sides of the neck. A third pair of thinner, parallel stripes runs down the neck between the nuchal stripes, extending to about one fourth of the mid-dorsal line, where they vanish or diverge as the first row of flank spots. The black mid-dorsal line is continuous and is flanked on each side by four rows of oblong to squared spots, and by a few small-scattered spots below. There is a dorsal erectile crest. The face has a dark mask and a pair of white sub-ocular spots. The tail has seven to nine black rings, alternating with pale rings; the intervening white spaces are pigmented with a brownish tinge on the dorsal midline. The width of the pale rings relative to the dark rings in the middle of the tail is 50-75%; the tip of the tail is dark. The hindlimbs and forelimbs are black; there are white hairs on the metacarpals and metatarsals. [he posterior parts of the feet are dark. There are two pairs of teats. The posterior chamber of the auditory bulla is not ventrally inflated and has a continuous curve line on the external side. The ratio between the inter-orbital constriction and frontal width is 1-00 + 0-12. Dental formula: 13/3, C1/1,P 4/4, M 2/2 = 40. in Viverridae
Distribution. Angola, DR Congo, Malawi, Mozambique, Tanzania, and Zambia. Description. Head-body 46:5-47-8 cm (males), 44-45-5 cm (females), tail 40-43 cm (males), 38-39 cm (females), hindfoot 8:7-9-8 cm (males), 8-9 cm (females), ear 4-7-5-4 cm (males), 5-1-5-8 cm (females); weight 1-3-2 kg. The coat color is pale ocher, with brownish or grayish tones; melanistic individuals are quite common. The throat and chest are blackish, and the ventral pelage varies from creamy white to dirty white. The stripes and spots on the body vary from different hues of brown to black. The nuchal stripes run as two parallel lines from the nape to the shoulders, where they diverge and enlarge towards the elbows; they are not so conspicuously marked as in other genet species. Below them, a pair of thinner stripes and small spots are scattered on the shoulders and sides of the neck. A third pair of thinner, parallel stripes runs down the neck between the nuchal stripes, extending to about one fourth of the mid-dorsal line, where they vanish or diverge as the first row of flank spots. The black mid-dorsal line is continuous and is flanked on each side by four rows of oblong to squared spots, and by a few small-scattered spots below. There is a dorsal erectile crest. The face has a dark mask and a pair of white sub-ocular spots. The tail has seven to nine black rings, alternating with pale rings; the intervening white spaces are pigmented with a brownish tinge on the dorsal midline. The width of the pale rings relative to the dark rings in the middle of the tail is 50-75%; the tip of the tail is dark. The hindlimbs and forelimbs are black; there are white hairs on the metacarpals and metatarsals. [he posterior parts of the feet are dark. There are two pairs of teats. The posterior chamber of the auditory bulla is not ventrally inflated and has a continuous curve line on the external side. The ratio between the inter-orbital constriction and frontal width is 1-00 + 0-12. Dental formula: 13/3, C1/1,P 4/4, M 2/2 = 40.
On following pages: 423. Tate's Rice Rat (Hylaeamystate); 424. Sowbug Rice Rat (Hylaeamys oniscus); 425. Bolivian Rice Rat (Hylaeamys acritus); 426. Atlantic Forest Rice Rat (Hylaeamys laticeps); 427. Fulvous Pygmy Rice Rat (Oligoryzomys fulvescens); 428. Costa Rican Pygmy Rice Rat (Oligoryzomys costaricensis); 429. Sprightly Pygmy Rice Rat (Oligoryzomys vegetus); 430. Delicate Pygmy Rice Rat (Oligoryzomys delicatus); 431. Grayish Pygmy Rice Rat (Oligoryzomys griseolus); 432. Hairy Pygmy Rice Rat (Oligoryzomys messorius); 433. Tschudi''s Pygmy Rice Rat (Oligoryzomys destructor); 434. Sandy Pygmy Rice Rat (Oligoryzomys arenalis); 435. Andean Pygmy Rice Rat (Oligoryzomys andinus); 436. Small-eared Pygmy Rice Rat (Oligoryzomys microtis); 437. Utiariti Pygmy Rice Rat (Oligoryzomys utiaritensis); 438. Straw-colored Pygmy Rice Rat (Oligoryzomys stramineus); 439. Mato Grosso Pygmy Rice Rat (Oligoryzomys mattogrossae); 440. Moojen's Pygmy Rice Rat (Oligoryzomys moojeni); 441. Highlands Pygmy Rice Rat (Oligoryzomys rupestris); 442. Black-footed Pygmy Rice Rat (Oligoryzomys nigripes); 443. San Javier's Pygmy Rice Rat (Oligoryzomys brendae); 444. Chacoan Pygmy Rice Rat (Oligoryzomys chacoensis); 445. Fornes's Pygmy Rice Rat (Oligoryzomys fornesi); 446. Yellow Pygmy Rice Rat (Oligoryzomys flavescens); 447. Long-tailed Pygmy Rice Rat (Oligoryzomys longicaudatus); 448. Painted Bristly Mouse (Neacomys pictus); 449. Narrow-footed Bristly Mouse (Neacomys tenuipes); 450. Guianan Bristly Mouse (Neacomys guianae); 451. Paracou Bristly Mouse (Neacomys paracou); 452. Dubost's Bristly Mouse (Neacomys dubosti); 453. Large Bristly Mouse (Neacomys spinosus); 454. Pleasant Bristly Mouse (Neacomys amoenus), 455. Vargas Llosa''s Bristly Mouse (Neacomys vargasllosai); 456. Minute Bristly Mouse (Neacomys minutus); 457. Musser's Bristly Mouse (Neacomys musseri). in Cricetidae
On following pages: 423. Tate's Rice Rat (Hylaeamystate); 424. Sowbug Rice Rat (Hylaeamys oniscus); 425. Bolivian Rice Rat (Hylaeamys acritus); 426. Atlantic Forest Rice Rat (Hylaeamys laticeps); 427. Fulvous Pygmy Rice Rat (Oligoryzomys fulvescens); 428. Costa Rican Pygmy Rice Rat (Oligoryzomys costaricensis); 429. Sprightly Pygmy Rice Rat (Oligoryzomys vegetus); 430. Delicate Pygmy Rice Rat (Oligoryzomys delicatus); 431. Grayish Pygmy Rice Rat (Oligoryzomys griseolus); 432. Hairy Pygmy Rice Rat (Oligoryzomys messorius); 433. Tschudi''s Pygmy Rice Rat (Oligoryzomys destructor); 434. Sandy Pygmy Rice Rat (Oligoryzomys arenalis); 435. Andean Pygmy Rice Rat (Oligoryzomys andinus); 436. Small-eared Pygmy Rice Rat (Oligoryzomys microtis); 437. Utiariti Pygmy Rice Rat (Oligoryzomys utiaritensis); 438. Straw-colored Pygmy Rice Rat (Oligoryzomys stramineus); 439. Mato Grosso Pygmy Rice Rat (Oligoryzomys mattogrossae); 440. Moojen's Pygmy Rice Rat (Oligoryzomys moojeni); 441. Highlands Pygmy Rice Rat (Oligoryzomys rupestris); 442. Black-footed Pygmy Rice Rat (Oligoryzomys nigripes); 443. San Javier's Pygmy Rice Rat (Oligoryzomys brendae); 444. Chacoan Pygmy Rice Rat (Oligoryzomys chacoensis); 445. Fornes's Pygmy Rice Rat (Oligoryzomys fornesi); 446. Yellow Pygmy Rice Rat (Oligoryzomys flavescens); 447. Long-tailed Pygmy Rice Rat (Oligoryzomys longicaudatus); 448. Painted Bristly Mouse (Neacomys pictus); 449. Narrow-footed Bristly Mouse (Neacomys tenuipes); 450. Guianan Bristly Mouse (Neacomys guianae); 451. Paracou Bristly Mouse (Neacomys paracou); 452. Dubost's Bristly Mouse (Neacomys dubosti); 453. Large Bristly Mouse (Neacomys spinosus); 454. Pleasant Bristly Mouse (Neacomys amoenus), 455. Vargas Llosa''s Bristly Mouse (Neacomys vargasllosai); 456. Minute Bristly Mouse (Neacomys minutus); 457. Musser's Bristly Mouse (Neacomys musseri).
Distribution. Known only from type locality on S coast of Seram I, Indonesia. Descriptive notes. Head-body 123 mm, tail 128 mm, ear 14-6 mm, hindfoot 26-2 mm; weight 65 g (all mensural data are from holotype). Pavel's Seram Mosaic-tailed Rat is very small-bodied, with dorsal pelage soft and brightly colored rufescent reddish brown, hairs with graybases, and venter contrastingly pure white; tail is slightly longer than head-body length, all black in color, tail scales raised, one hair per scale, scale hairs very short. Upper surfaces of feet are dark gray; hindfeet broad, with first digit long. Cranium is relatively narrow, with nasal profile flat; teeth very small. Single known specimen (the holotype), a pregnant female, has four mammae. in Muridae
Distribution. Known only from type locality on S coast of Seram I, Indonesia. Descriptive notes. Head-body 123 mm, tail 128 mm, ear 14-6 mm, hindfoot 26-2 mm; weight 65 g (all mensural data are from holotype). Pavel's Seram Mosaic-tailed Rat is very small-bodied, with dorsal pelage soft and brightly colored rufescent reddish brown, hairs with graybases, and venter contrastingly pure white; tail is slightly longer than head-body length, all black in color, tail scales raised, one hair per scale, scale hairs very short. Upper surfaces of feet are dark gray; hindfeet broad, with first digit long. Cranium is relatively narrow, with nasal profile flat; teeth very small. Single known specimen (the holotype), a pregnant female, has four mammae.
FIGURE 6. Echinothrix calamaris. Color morphotypes. A. Black and white spine form. B. White spine form. C in New Ecological Observations and Occurrence for Asteroidea and Echinoidea in Hong Kong
FIGURE 6. Echinothrix calamaris. Color morphotypes. A. Black and white spine form. B. White spine form. C. Banded spine form. Photographer: Sam King Fung Yiu.
Black Patients' Lived Experiences and Perceptions of Skin of Color Clinics
ClinicalTrials.gov study NCT02375659. IPD Sharing: Not stated. Countries: 1. Publications: 8.
Data from: Not everything is black and white: color and behavioral variation reveal a continuum between cryptic and aposematic strategies in a polymorphic poison frog
Open the record for dataset details and reuse information.
Data from: Using river color to predict Amazonian floodplain forest avifauna in the world’s largest black-water river basin
Open the record for dataset details and reuse information.
Data from: Structurally assisted super black in colorful peacock spiders
Male peacock spiders (Maratus, Salticidae) compete to attract female mates using elaborate, sexually-selected displays. They evolved both brilliant color and velvety black. Here we use scanning electron microscopy (SEM), hyperspectral imaging, and finite-difference time-domain (FDTD) optical modeling to investigate the deep black surfaces of peacock spiders. We found that super black regions reflect <0.5% of light (for a 30° collection angle) in Maratus speciosus (0.44%) and Maratus karrie (0.35%) due to microscale structures. Both species evolved unusually high, tightly packed cuticular bumps (microlens arrays), and M. karrie has an additional dense covering of black brush-like scales atop the cuticle. Our optical models show that the radius and height of spider microlenses achieve a balance between (i) decreased surface reflectance and (ii) enhanced melanin absorption (through multiple scattering, diffraction out of the acceptance cone of female eyes, and increased path length of light through absorbing melanin pigments). The birds-of-paradise (Paradiseidae), ecological analogues of peacock spiders, also evolved super black near bright color patches. Super black locally eliminates white specular highlights, reference points used to calibrate color perception, making nearby colors appear brighter, even luminous, to vertebrates. We propose that this pre-existing, qualitative sensory experience—"sensory bias"—is also found in spiders, leading to the convergent evolution of super black for mating displays in jumping spiders.
What makes a mimic? Orange, red, and black color production in the mimic poison frog (Ranitomeya imitator)
Open the record for dataset details and reuse information.
◂Fig. 1 Live photos and dissection of parasitized Aphrodita longipalpa and Veneriserva pygoclava. A Ventral view of A. longipalpa. B Dorsal view of A. longipalpa with removed feltage chaetae, revealing the parasite visible through the body wall. C Ventrally dissected A. longipalpa, exposing the sizable female parasite. Veneriserva pygoclava individuals within the host are indicated by arrowheads. D Juvenile female V. pygoclava, with developing oocytes visible through the body wall along the mid-dorsal orange line. E Female V. pygoclava showing the mid-dorsal orange pigmentation and the white mark at the base of the prostomium. F Male V. pygoclava. G A large female and smaller male V. pygoclava, extracted from the same host. The pygidium is club-shaped in both males and females and juveniles. H Juvenile V. pygoclava shown from multiple angles, characterized by a complete white coloration; black jaws are magnified in panel in Hardly Venus's servant-morphological adaptations of Veneriserva to an endoparasitic lifestyle and its phylogenetic position within Dorvilleidae (Annelida)
◂Fig. 1 Live photos and dissection of parasitized Aphrodita longipalpa and Veneriserva pygoclava. A Ventral view of A. longipalpa. B Dorsal view of A. longipalpa with removed feltage chaetae, revealing the parasite visible through the body wall. C Ventrally dissected A. longipalpa, exposing the sizable female parasite. Veneriserva pygoclava individuals within the host are indicated by arrowheads. D Juvenile female V. pygoclava, with developing oocytes visible through the body wall along the mid-dorsal orange line. E Female V. pygoclava showing the mid-dorsal orange pigmentation and the white mark at the base of the prostomium. F Male V. pygoclava. G A large female and smaller male V. pygoclava, extracted from the same host. The pygidium is club-shaped in both males and females and juveniles. H Juvenile V. pygoclava shown from multiple angles, characterized by a complete white coloration; black jaws are magnified in panel
Data from: Structurally assisted super black in colorful peacock spiders
Open the record for dataset details and reuse information.
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.