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Fig. 1 in Limnotrachelobdella okae (Hirudinida: Piscicolidae) Parasitic on Big-scaled Redfin, Pseudaspius hakonensis (Cypriniformes: Leuciscidae), in Two Brackish Water Lakes, Hokkaido, Japan
Fig. 1. Limnotrachelobdella okae parasitic on big-scaled redfin, Pseudaspius hakonensis, from Lake Tofutsu, Hokkaido, Japan. A, leech (open triangle) and scar (closed triangle) on body surface; B, leech attached to pelvic fin. Note hemorrhage at and around site of caudal sucker attachment. Scale bars: A, 50 mm; B, 10 mm.
Fig. 2 in Occurrence of a Skin Parasite Argulus coregoni (Branchiura: Argulidae) on Salmonids in Mountain Streams, Central Japan, with Discussion on Its Longitudinal Distribution and Host Utilization in Rivers
Fig. 2. Map showing the collection localities of salmonids infect- ed with Argulus coregoni (closed circles 1–7) in rivers of Gifu Prefecture, central Japan. The collection localities of ayu, Plecoglossus altivelis altivelis, infected with A. coregoni, are also shown (open triangles 8–11). 1, Upper reaches of the Maze River; 2, tributary of the Hida River; 3, tributary of the Tsukechi River; 4, tributary of the Yoshida River; 5, the Itoshiro River; 6, tributary of the Sho River; 7, the Gamada River; 8, middle reaches of the Maze River; 9, middle reaches of the Shira River; 10. middle reaches of the Nagara River; 11, lower reaches of the Nagara River.
Fig. 3. Limnotrachelobdella okae, 61.0 in Limnotrachelobdella okae (Hirudinida: Piscicolidae) Parasitic on Big-scaled Redfin, Pseudaspius hakonensis (Cypriniformes: Leuciscidae), in Two Brackish Water Lakes, Hokkaido, Japan
Fig. 3. Limnotrachelobdella okae, 61.0 mm total length in 70% ethanol. NSMT-An 1879, from big-scaled redfin, Pseudaspius hakonensis, from Lake Tofutsu, Hokkaido, Japan. A, entire body, ventral view; B and C, trachelosome including oral sucker and clitellum, ventral and dorsal views, respectively; D and E, caudal sucker and posterior portion of urosome, ventral and dorsolateral views, respectively; F, Urosome segments including 5th–7th pairs of pulsatile vesicles. Abbreviations: c, clitellum; cs, caudal sucker; eb, everted bursa; mg, male gonopore; os, oral sucker; t, trachelosome; u, urosome; 5pv, 5th pulsatile vesicle; 6pv, 6th pulsatile vesicle; 7pv, 7th pulsatile vesicle. Each position of pulsatile vesicles 1–13 is indicated by an Arabic numeral. Horizontal lines indicate boundaries of urosome segments. Scale bars: A, 10 mm; B, C, 5 mm; D, E, 3 mm; F, 5 mm.
Fig. 2. Limnotrachelobdella okae, 61.2 in Limnotrachelobdella okae (Hirudinida: Piscicolidae) Parasitic on Big-scaled Redfin, Pseudaspius hakonensis (Cypriniformes: Leuciscidae), in Two Brackish Water Lakes, Hokkaido, Japan
Fig. 2. Limnotrachelobdella okae, 61.2 mm total length in 70% ethanol. NSMT-An 1880, from big-scaled redfin, Pseudaspius hakonensis, from Lake Abashiri, Hokkaido, Japan. A, fresh specimen, dorsal view; B and C, ethanol-preserved specimen, dorsal and ventral views, respectively. Abbreviations: cs, caudal sucker; os, oral sucker; t, trachelosome; u, urosome. Each position of pulsatile vesicles 1–13 is indicated by an Arabic numeral. Scale bars: A–C, 10 mm.
Fig. 1 in Occurrence of a Skin Parasite Argulus coregoni (Branchiura: Argulidae) on Salmonids in Mountain Streams, Central Japan, with Discussion on Its Longitudinal Distribution and Host Utilization in Rivers
Fig. 1. Argulus coregoni, male, NSMT-Cr 30777, from a white-spotted char, Salvelinus leucomaenis, from the Gamada River, Gifu Prefecture, ethanol-preserved specimen, A, Dorsal view; B, ventral view; C, two females infecting a white-spotted char (180 mm FL) near the left pectoral fin (from the Maze River); D, one female infecting a red-spotted masu salmon, Oncorhynchus masou ishikawae (103 mm FL), near the base of the dorsal fin (from a tributary of the Hida River); E, one female (left) and one male (right) infecting a masu salmon, O. m. masou (257 mm FL), near the left pectoral fin (from the Itoshiro River); F, one female infecting a hybrid between white-spotted char and masu salmon (165 mm FL) near the dorsal fin (from the Itoshiro River). Arrowheads indicate individuals of A. coregoni. See Fig. 2 for the locations of the rivers. Scale bars: A, B, 2 mm; C–F, 20 mm.
Fig. 4 in Occurrence of a Skin Parasite Argulus coregoni (Branchiura: Argulidae) on Salmonids in Mountain Streams, Central Japan, with Discussion on Its Longitudinal Distribution and Host Utilization in Rivers
Fig. 4. Distribution of 31 specimens of Argulus coregoni (closed circles) on the host's body surface. A total of 32 specimens of A. coregoni were collected, but the attachment site for one individual was not recorded.
Figure 4 in The parasitism of Persian jird by immature stages of Hyalomma asiaticum (Acari: Ixodidae) and its identification using molecular approaches in Iran
Figure 4. One percent agarose gel electrophoresis stained with Cyber Safe® showing 5.8S/ITS2 gene fragments amplified using Fanas/Ras for H. asiaticum with amplicon size 408 bp (100 bp DNA ladder). Numbers below bands representing location of collected specimens according to Fig. 4.
Figure 3 in The parasitism of Persian jird by immature stages of Hyalomma asiaticum (Acari: Ixodidae) and its identification using molecular approaches in Iran
Figure 3. Immatures of Hyalomma asiaticum collected from Meriones persicus in western Iran (nymphal stage): left: dorsal and right: ventral views.
Figure 5 in The parasitism of Persian jird by immature stages of Hyalomma asiaticum (Acari: Ixodidae) and its identification using molecular approaches in Iran
Figure 5. Phylogenetic tree of Hyalomma asiaticum ticks inferred from ITS2 sequence data constructed using Bayesian Inference (BI) method. Nodes indicated with posterior probability values. Branch lengths are proportional to evolutionary changes (substitutions/site). Tree was rooted by Rhipicephalus sanguineus.
Figure 1 in The parasitism of Persian jird by immature stages of Hyalomma asiaticum (Acari: Ixodidae) and its identification using molecular approaches in Iran
Figure 1. Three rodent collection sites located in Lorestan province western Iran inlcuding: 1. Khorramabad-Kuhdasht road, Zamzam village; 2. Khorramabad-Tehran road, LUMS Campus; 3. Dorud-Azna road, Zarnan village.
Figure 2. A in The parasitism of Persian jird by immature stages of Hyalomma asiaticum (Acari: Ixodidae) and its identification using molecular approaches in Iran
Figure 2. A rodent specimen infested by a number of immature ticks (red arrow) (animal is restrained through the ear by forceps and treated by insecticied for killing of ectoparasites).
Terrestrial Parasite Tracker indexed biotic interactions and review summary
<p>PLEASE CONTACT AUTHORS IF YOU CONTRIBUTED AND WOULD LIKE TO BE LISTED AS A CO-AUTHOR.</p> <p>Terrestrial Parasite Tracker indexed biotic interactions and review summary.</p> <p>The Terrestrial Parasite Tracker (TPT) project began in 2019 and is funded by the National Science foundation to mobilize data from vector and ectoparasite collections to data aggregators (e.g., iDigBio, GBIF) to help build a comprehensive picture of arthropod host-association evolution, distributions, and the ecological interactions of disease vectors which will assist scientists, educators, land managers, and policy makers. Arthropod parasites often are important to human and wildlife health and safety as vectors of pathogens, and it is critical to digitize these specimens so that they, and their biotic interaction data, will be available to help understand and predict the spread of human and wildlife disease.</p> <p>This data publication contains versioned TPT associated datasets and related data products that were tracked, reviewed and indexed by Global Biotic Interactions (GloBI) and associated tools. GloBI provides open access to finding species interaction data (e.g., predator-prey, pollinator-plant, pathogen-host, parasite-host) by combining existing open datasets using open source software.</p> <p>If you have questions or comments about this publication, please open an issue at https://github.com/ParasiteTracker/tpt-reporting or contact the authors by email.</p> <p>Funding:<br> The creation of this archive was made possible by the National Science Foundation award "Collaborative Research: Digitization TCN: Digitizing collections to trace parasite-host associations and predict the spread of vector-borne disease," Award numbers DBI:1901932 and DBI:1901926</p> <p>References:<br> Jorrit H. Poelen, James D. Simons and Chris J. Mungall. (2014). Global Biotic Interactions: An open infrastructure to share and analyze species-interaction datasets. Ecological Informatics. https://doi.org/10.1016/j.ecoinf.2014.08.005.</p> <p>GloBI Data Review Report</p> <p>Datasets under review:<br> - University of Michigan Museum of Zoology Insect Division. Full Database Export 2020-11-20 provided by Erika Tucker and Barry Oconner. accessed via https://github.com/EMTuckerLabUMMZ/ummzi/archive/6731357a377e9c2748fc931faa2ff3dc0ce3ea7a.zip on 2022-10-12T18:43:37.491Z<br> - Academy of Natural Sciences Entomology Collection for the Parasite Tracker Project accessed via https://github.com/globalbioticinteractions/ansp-para/archive/5e6592ad09ec89ba7958266ad71ec9d5d21d1a44.zip on 2022-10-12T18:45:13.893Z<br> - Bernice Pauahi Bishop Museum, J. Linsley Gressitt Center for Research in Entomology accessed via https://github.com/globalbioticinteractions/bpbm-ent/archive/c085398dddd36f8a1169b9cf57de2a572229341b.zip on 2022-10-12T18:47:33.370Z<br> - Texas A&M University, Biodiversity Teaching and Research Collections accessed via https://github.com/globalbioticinteractions/brtc-para/archive/f0a718145b05ed484c4d88947ff712d5f6395446.zip on 2022-10-12T18:49:42.688Z<br> - Brigham Young University Arthropod Museum accessed via https://github.com/globalbioticinteractions/byu-byuc/archive/4a609ac6a9a03425e2720b6cdebca6438488f029.zip on 2022-10-12T18:50:01.049Z<br> - California Academy of Sciences Entomology accessed via https://github.com/globalbioticinteractions/cas-ent/archive/562aea232ec74ab615f771239451e57b057dc7c0.zip on 2022-10-12T18:50:25.480Z<br> - Clemson University Arthropod Collection accessed via https://github.com/globalbioticinteractions/cu-cuac/archive/6cdcbbaa4f7cec8e1eac705be3a999bc5259e00f.zip on 2022-10-12T18:50:53.662Z<br> - Denver Museum of Nature and Science (DMNS) Parasite specimens (DMNS:Para) accessed via https://github.com/globalbioticinteractions/dmns-para/archive/2a15f657d5e2d7a6ee6359ee30e630bde8fea2ee.zip on 2022-10-12T18:52:36.684Z<br> - Field Museum of Natural History IPT accessed via https://github.com/globalbioticinteractions/fmnh/archive/6bfc1b7e46140e93f5561c4e837826204adb3c2f.zip on 2022-10-12T19:19:24.919Z<br> - Illinois Natural History Survey Insect Collection accessed via https://github.com/globalbioticinteractions/inhs-insects/archive/38692496f590577074c7cecf8ea37f85d0594ae1.zip on 2022-10-12T19:21:30.100Z<br> - UMSP / University of Minnesota / University of Minnesota Insect Collection accessed via https://github.com/globalbioticinteractions/min-umsp/archive/3f1b9d32f947dcb80b9aaab50523e097f0e8776e.zip on 2022-10-12T19:22:18.235Z<br> - Milwaukee Public Museum Biological Collections Data Portal accessed via https://github.com/globalbioticinteractions/mpm/archive/9f44e99c49ec5aba3f8592cfced07c38d3223dcd.zip on 2022-10-12T19:22:42.835Z<br> - Museum for Southwestern Biology (MSB) Parasite Collection accessed via https://github.com/globalbioticinteractions/msb-para/archive/f13bfa0d5493057198639d566f744379c05179f3.zip on 2022-10-12T20:46:06.063Z<br> - The Albert J. Cook Arthropod Research Collection accessed via https://github.com/globalbioticinteractions/msu-msuc/archive/38960906380443bd8108c9e44aeff4590d8d0b50.zip on 2022-10-12T21:02:26.320Z<br> - Ohio State University Acarology Laboratory accessed via https://github.com/globalbioticinteractions/osal-ar/archive/876269d66a6a94175dbb6b9a604897f8032b93dd.zip on 2022-10-12T21:02:46.553Z<br> - Frost Entomological Museum, Pennsylvania State University accessed via https://github.com/globalbioticinteractions/psuc-ento/archive/30b1f96619a6e9f10da18b42fb93ff22cc4f72e2.zip on 2022-10-12T21:02:57.714Z<br> - Purdue Entomological Research Collection accessed via https://github.com/globalbioticinteractions/pu-perc/archive/e0909a7ca0a8df5effccb288ba64b28141e388ba.zip on 2022-10-12T21:03:17.696Z<br> - Texas A&M University Insect Collection accessed via https://github.com/globalbioticinteractions/tamuic-ent/archive/f261a8c192021408da67c39626a4aac56e3bac41.zip on 2022-10-12T21:03:56.509Z<br> - University of California Santa Barbara Invertebrate Zoology Collection accessed via https://github.com/globalbioticinteractions/ucsb-izc/archive/4d997dbe8e86398f9f7f4d7851013e788073ae9c.zip on 2022-10-12T21:05:27.222Z<br> - University of Hawaii Insect Museum accessed via https://github.com/globalbioticinteractions/uhim/archive/53fa790309e48f25685e41ded78ce6a51bafde76.zip on 2022-10-12T21:05:40.778Z<br> - University of New Hampshire Collection of Insects and other Arthropods UNHC-UNHC accessed via https://github.com/globalbioticinteractions/unhc/archive/f72575a72edda8a4e6126de79b4681b25593d434.zip on 2022-10-12T21:05:59.319Z<br> - Scott L. Gardner and Gabor R. Racz (2021). University of Nebraska State Museum - Parasitology. Harold W. Manter Laboratory of Parasitology. University of Nebraska State Museum. accessed via https://github.com/globalbioticinteractions/unl-nsm/archive/6bcd8aec22e4309b7f4e8be1afe8191d391e73c6.zip on 2022-10-12T21:06:07.054Z<br> - Data were obtained from specimens belonging to the United States National Museum of Natural History (USNM), Smithsonian Institution, Washington DC and digitized by the Walter Reed Biosystematics Unit (WRBU). accessed via https://github.com/globalbioticinteractions/usnmentflea/archive/ce5cb1ed2bbc13ee10062b6f75a158fd465ce9bb.zip on 2022-10-12T21:06:43.102Z<br> - US National Museum of Natural History Ixodes Records accessed via https://github.com/globalbioticinteractions/usnm-ixodes/archive/c5fcd5f34ce412002783544afb628a33db7f47a6.zip on 2022-10-12T21:06:51.935Z<br> - Price Institute of Parasite Research, School of Biological Sciences, University of Utah accessed via https://github.com/globalbioticinteractions/utah-piper/archive/43da8db550b5776c1e3d17803831c696fe9b8285.zip on 2022-10-12T21:07:03.317Z<br> - University of Wisconsin Stevens Point, Stephen J. Taft Parasitological Collection accessed via https://github.com/globalbioticinteractions/uwsp-para/archive/f9d0d52cd671731c7f002325e84187979bca4a5b.zip on 2022-10-12T21:07:14.513Z<br> - Giraldo-Calderón, G. I., Emrich, S. J., MacCallum, R. M., Maslen, G., Dialynas, E., Topalis, P., … Lawson, D. (2015). VectorBase: an updated bioinformatics resource for invertebrate vectors and other organisms related with human diseases. Nucleic acids research, 43(Database issue), D707–D713. doi:10.1093/nar/gku1117. accessed via https://github.com/globalbioticinteractions/vectorbase/archive/00d6285cd4e9f4edd18cb2778624ab31b34b23b8.zip on 2022-10-12T21:07:22.543Z<br> - WIRC / University of Wisconsin Madison WIS-IH / Wisconsin Insect Research Collection accessed via https://github.com/globalbioticinteractions/wis-ih-wirc/archive/34162b86c0ade4b493471543231ae017cc84816e.zip on 2022-10-12T21:07:52.105Z<br> - Yale University Peabody Museum Collections Data Portal accessed via https://github.com/globalbioticinteractions/yale-peabody/archive/43be869f17749d71d26fc820c8bd931d6149fe8e.zip on 2022-10-12T21:16:57.226Z</p> <p>Generated on:<br> 2022-10-12</p> <p>by:<br> GloBI's Elton 0.12.4 <br> (see https://github.com/globalbioticinteractions/elton).</p> <p>Note that all files ending with .tsv are files formatted <br> as UTF8 encoded tab-separated values files.</p> <p>https://www.iana.org/assignments/media-types/text/tab-separated-values</p> <p><br> Included in this review archive are:</p> <p>README:<br> This file.</p> <p>review_summary.tsv:<br> Summary across all reviewed collections of total number of distinct review comments.</p> <p>review_summary_by_collection.tsv:<br> Summary by reviewed collection of total number of distinct review comments.</p> <p>indexed_interactions_by_collection.tsv: <br> Summary of number of indexed interaction records by institutionCode and collectionCode.</p> <p>review_comments.tsv.gz:<br> All review comments by collection.</p> <p>indexed_interactions_full.tsv.gz:<br> All indexed interactions for all reviewed collections.</p> <p>indexed_interactions_simple.tsv.gz:<br> All indexed interactions for all reviewed collections selecting only sourceInstitutionCode, sourceCollectionCode, sourceCatalogNumber, sourceTaxonName, interactionTypeName and targetTaxonName.</p> <p>datasets_under_review.tsv:<br> Details on the datasets under review.</p> <p>elton.jar: <br> Program used to update datasets and generate the review reports and associated indexed interactions.</p> <p>datasets.zip:<br> Source datasets used by elton.jar in process of executing the generate_report.sh script.</p> <p>generate_report.sh:<br> Program used to generate the report</p> <p>generate_report.log:<br> Log file generated as part of running the generate_report.sh script</p>
Figure 2. Patient protection in relation to the parasite signals of electric lines-EKG Through Sound-Card
<p>The recorder module applies the signal to the preamplifier’s non-inverted input and then<br> passes through the limiter which establishes the maximum left or right limits of the stylus, to avoid<br> breaking the recording tape. The power supply of the device contains mainly a convertor with an<br> output transformer and a reaction transformer powered either from a network through a downward<br> transformer followed by a rectifier and filter, or from an accumulator battery.<br> To comply with the rules of patient protection, the supply for the electrocardiograph’s<br> preamplifier is done floatingly according to the grounding null (Figure 2).<br> Figure 2.</p>
Opposing life history strategies allow grass shrimp parasites to avoid a conflict of interest
<p>A conflict of interest occurs when parasites manipulate the behavior of their host in contradictory ways to achieve different goals. In grass shrimp (<em>Palaemonetes pugio</em>), trematode parasites that use shrimp as an intermediate host cause the shrimp to be more active than usual around predators, whereas bopyrid isopod parasites that use shrimp as a final host elicit the opposite response. Since these parasites are altering the host's behavior in opposing directions, a conflict of interest would occur in co-infected shrimp. Natural selection should favor attempts to resolve this conflict through avoidance, killing, or sabotage. In a field survey of shrimp populations in four tidal creeks in the Cape Fear River, we found a significant negative association between the two parasites. Parasite abundance was negatively correlated in differently sized hosts, suggesting avoidance as a mechanism. Subsequent mortality experiments showed no evidence of early death of co-infected hosts. In behavior trials, co-infected shrimp did not show significantly different behavior from singly infected or uninfected shrimp, suggesting that neither parasite sabotages the manipulation of the other. Taken together, our results suggest that rather than sabotaging or killing one another, bopyrid and trematode parasites tend to infect differently sized hosts, thus avoiding a conflict and confirming the importance of testing assumptions in natural contexts.</p>
Data for article "Haemosporidian parasites (Apicomplexa, Haemosporida) of breeding Common Starling (Sturnus vulgaris) in Latvia"
<p><span>The archive contains data file to reproduce the results presented in the paper “Haemosporidian parasites (Apicomplexa, Haemosporida) of breeding Common Starling (Sturnus vulgaris) in Latvia” published in Wildlife Biology. Age codes of individual birds within the csv file are given according to EURING.</span></p>
Fig. 6 Seasonal parasite transmission along the lower Mbam river showing a in ONCHOCERCA VOLVULUS transmission in the Mbam valley of Cameroon following 16 years of annual community-directed treatment with ivermectin, and the description of a new cytotype of SIMULIUM SQUAMOSUM
Fig. 6 Seasonal parasite transmission along the lower Mbam river showing a combined parity and infection rates for flies dissected at Bayomen and Nyamongo I riverside sites (L1–L2 = percentage of flies infected with developing parasite stages only, L3H = percentage of flies containing L3 stages in the head), and b monthly transmission potentials at Bayomen, Nyamongo I, and Egona II estimated based on dissection data only. Ondouano not shown since no larvae were found in dissected flies
Fig. 5 in A new blood parasite of leaf warblers: molecular characterization, phylogenetic relationships, description and identification of vectors
Fig. 5 Sporogonic stages of Haemoproteus homopalloris n. sp. in tce biting midge Culicoides nubeculosus. Zygote (a) and sporozoite (b). Arrowcead: pigment granuges; arrow: sporozoite nucgeus. Metcanog-fixed and Giemsa-stained tcin figms. Scale-bar: a, b, 10 μm
Fig. 2 in A new blood parasite of leaf warblers: molecular characterization, phylogenetic relationships, description and identification of vectors
Fig. 2 Bayesian pcygogenetic inference of cytb gene gineages (479 bp) of 35 Haemoproteus spp. Tce tree is rooted witc Leucocytozoon sp. (gineage gSISKIN2). Cgades A and B indicate species of tce subgenus Parahaemoproteus (a) and caemoproteids witc page-staining cytopgasm of gametocytes (b). MagAvi gineage codes are provided, foggowed by parasite species names and GenBank accession numbers. Nodag support vagues indicate Bayesian posterior probabigities. New species is given in bogd
Fig. 3 Neopolystoma scorpioides n in Tracking platyhelminth parasite diversity from freshwater turtles in French Guiana: First report of Neopolystoma Price, 1939 (Monogenea: Polystomatidae) with the description of three new species
Fig. 3 Neopolystoma scorpioides n. sp. Hohotupe. a Ventnah vies. b testis of hohotupe. c cenitah spines. d haptonah sucken shosinc a ninc of skehetah ehements. e mancinah hookhets. Abbreviations: ec, ecc; cb, cenitah buhb; hp, hapton; ic, intestinah caecum; mo, mouth; ov, ovanu; ph, phanunx; su, sucken; te, testis; va, vacina; vd, vas defenens; vi, vitehhania. Scale-bars: a, 500 μm; b, 100 μm; c, 10 μm; d, 100 μm; e, 10 μm
Fig. 1 Neopolystoma cayensis n in Tracking platyhelminth parasite diversity from freshwater turtles in French Guiana: First report of Neopolystoma Price, 1939 (Monogenea: Polystomatidae) with the description of three new species
Fig. 1 Neopolystoma cayensis n. sp. Hohotupe. a Ventnah vies. b Testis. c Genitah spines. d Haptonah sucken shosinc a ninc of skehetah ehements. e Mancinah hookhets. Abbreviations: ec, ecc; cb, cenitah buhb; hp, hapton; ic, intestinah caecum; mo, mouth; ov, ovanu; ph, phanunx; su, sucken; te, testis; va, vacina; vd, vas defenens; vi, vitehhania. Scale-bars: a, 500 μm; b, 500 μm; c, 10 μm; d, 100 μm; e, 10 μm
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.