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323 results for “Paleontology”
Data and code for: "Improving the relevance of paleontology to climate change policy"
<p>Data and code for the article: "Improving the relevance of paleontology to climate change policy". [Link here]</p>
Public database of geological-paleontological mapping in the surroundings of Vălioara
<p>The database contains the coordinates of the geological-paleontological mapping sites and measurements in the area of V<span>ă</span>lioara (Romania) from 2019 onwards. The Excel format file data tables contain in separate worksheets the localities, the measurements and the explanation of the mapping units. The coordinates are given in UTM34 coordinate system and also with latitude-longitude data (WGS84 datum).</p>
Aerial view of part of the Bisti badlands from an elevation of approximately 8500 feet. Exposed here are the Upper Cretaceous Fruitland and Kirtland Formations. Photograph taken the morning of 13 April 1992. Copyright © Paul L. Sealey. 1992. in Stratigraphy, paleontology and age of the Fruitland and Kirtland Formations (upper Cretaceous), San Juan Basin, New Mexico
Aerial view of part of the Bisti badlands from an elevation of approximately 8500 feet. Exposed here are the Upper Cretaceous Fruitland and Kirtland Formations. Photograph taken the morning of 13 April 1992. Copyright © Paul L. Sealey. 1992.
FIGURE 2 in Stratigraphy, paleontology and age of the Fruitland and Kirtland Formations (upper Cretaceous), San Juan Basin, New Mexico
FIGURE 2. Changing nomenclature of the Fruitland and Kirtland Formations. Note that older authors placed the Naashoibito Member within the Ojo Alamo Sandstone and that the boundary between the Fruitland and Kirtland Formations has been placed at the top of the Bisti Member (Bauer. 1916: Reeside. 1924). at the top of the highest thick coal (Fassett and Hinds, 1971) and herein at the base of the Bisti Member.
FIG. 8 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets
FIG. 8. — Hypotheses of primary venation homology of forewing of A, †Angarogryllus angaricus (Sharov 1968) (PIN 1873-16, †Protogryllidae, cf fig. 6A); B, Gryllotalpa sp. (MNHN-EO-ENSIF3938, Gryllotalpidae); C, Scapteriscus sp. (MNHN-EO-ENSIF3068, Gryllotalpidae). Abbreviations and colour code: see text. Scale bars: 1 mm.
FIG. 5 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets
FIG. 5. — Hypothesis of primary venation homology in male Grylloidea with particular forewing venation: A, B, species with 'shortened' wings; B, C, species with 'reduced' stridulatory apparatus. A, Landreva sp. (MNHN-EO-ENSIF9775, Gryllidae); B, Nemobius sylvestris (Bosc, 1792) (MNHN-EO-ENSIF9786, Trigonidiidae); C, Tafalisca lineatipes Bruner, 1916 (MNHN-EO-ENSIF9760, Oecanthidae); D, Aphonomorphus sp. (MNHN-EO-ENSIF9764, Oecanthidae). Abbreviations: 'ha', distally opened harp; 'mi' distally opened mirror; others and colour code: see text. Grey dash lines represent folds. Scale bars: 1 mm.
FIG. 1 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets
FIG. 1. — Theoretical pattern of venation of a gryllidean forewing (terminology after Béthoux & Nel [2002], modified after Schubnel et al. [2020]). Abbreviations and colour code: see text.
FIG. 7 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets
FIG. 7. — Hypothesis of primary venation homology of forewing of male Scapteriscus sp. MNHN-EO-ENSIF3069 (Gryllotalpidae). Abbreviations and colour code: see text. Grey dash lines represent folds. Scale bar: 1 mm.
APPENDIX 1 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets
<p>APPENDIX 1. — List of specimens observed in the MNHN Orthoptera collections. Supplementary figures gathered in Appendix 3.</p><table><thead><tr><th>Family, subfamily</th><th><b>Tribe</b></th><th><b>Genus Species</b></th><th><b>Identified</b></th><th>Sex</th><th><b>Inventory number</b></th><th><b>Origin</b></th><th><b>Figures</b></th></tr><tr><th colspan="8">OECANTHIDAE</th></tr></thead><tbody><tr><th>Oecanthinae</th><td>Oecanthini</td><td><i>Oecanthus rufescens</i> Serville, 1838</td><td>L. Desutter</td><td>♂</td><td>MNHN-EO-ENSIF9765</td><td>New Caledonia</td><td></td></tr><tr><th>Tafaliscinae</th><td>Tafaliscini</td><td><i>Tafalisca lineatipes</i> Bruner, 1916</td><td rowspan="2">L. Denadai de Campos</td><td>♂</td><td>MNHN-EO-ENSIF9760</td><td>Jamaica</td><td>5C; S3C</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td>Paroecanthini</td><td><i>Paroecanthus simplex</i> Gorochov, 2011</td><td>L. Denadai de Campos</td><td>♂</td><td>MNHN-EO-ENSIF9782</td><td>Mexique</td><td></td></tr><tr><th></th><td></td><td><i>Angustitrella vicina</i> (Chopard, 1912)</td><td>L. Denadai de Campos</td><td>♂</td><td>MNHN-EO-ENSIF9783</td><td>French Guiana</td><td></td></tr><tr><th></th><td></td><td><i>Ectotrypa olmeca</i> Saussure, 1874</td><td>L. Denadai de Campos</td><td>♂</td><td>MNHN-EO-ENSIF12163</td><td>Mexico</td><td>S2C</td></tr><tr><th>Podoscirtinae</th><td>Podoscirtini</td><td><i>Archenopterus bouensis</i> Otte, 1987</td><td>L. Desutter</td><td>♂</td><td>MNHN-EO-ENSIF3935</td><td>New Caledonia</td><td></td></tr><tr><th></th><td>Aphonomorphini</td><td><i>Aphonomorphus</i> sp.</td><td></td><td>♂</td><td>MNHN-EO-ENSIF9764</td><td>French Guiana</td><td>5D; S3D</td></tr><tr><th></th><td>Phyllogryllini</td><td><i>Phyllogryllus</i> sp.</td><td></td><td>♂</td><td>MNHN-EO-ENSIF9768</td><td>Guadeloupe</td><td>4B; S2B</td></tr><tr><th colspan="8">PHALANGOPSIDAE</th></tr><tr><th>Luzarinae</th><td>Luzarini</td><td><i>Luzara obscura</i> Desutter-Grandcolas, 1992</td><td>L. Desutter</td><td>♂</td><td>MNHN-EO-ENSIF5876</td><td>French Guiana</td><td></td></tr><tr><th></th><td></td><td><i>Lerneca fuscipennis</i> (Saussure, 1874)</td><td>L. Desutter</td><td>♂/♀</td><td>MNHN-EO-ENSIF9780, MNHN-EO-ENSIF9781</td><td>French Guiana</td><td>♂: 3B; S1D / ♀: S4A</td></tr><tr><th>Phalangopsinae</th><td>Phalangopsini</td><td><i>Endecous Itatibensis</i> Rehn, 1918</td><td>L. Desutter</td><td>♂</td><td>MNHN-EO-ENSIF9761</td><td>Brazil</td><td></td></tr><tr><th></th><td>Homoeogryllini</td><td rowspan="2"><i>Homoeogryllus</i> xanthographus Guérin-Ménevile, 1844</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td></td><td>L. Desutter</td><td>♂</td><td>MNHN-EO-ENSIF9779</td><td><i>Farm strain</i></td><td></td></tr><tr><th></th><td></td><td>orientalis Desutter, 1985</td><td>L. Desutter</td><td>♂</td><td>MNHN-EO-ENSIF3069</td><td>Mozambique</td><td></td></tr><tr><th></th><td></td><td><i>affinis lyristes</i> Gorochov, 1988</td><td>L. Desutter</td><td>♀</td><td>MNHN-EO-ENSIF9784</td><td>Rwanda</td><td>Fig. S4B</td></tr><tr><th>Paragryllinae</th><td>Aclodini</td><td><i>Paraclodes guyanensis</i> Desutter-Grandcolas, 1992</td><td>L. Desutter</td><td>♂</td><td>MNHN-EO-ENSIF9762</td><td>French Guiana</td><td></td></tr><tr><th></th><td>Paragryllini</td><td><i>Aclogryllus</i> sp ..</td><td>L. Desutter</td><td>♂</td><td>MNHN-EO-ENSIF9785</td><td>Equateur</td><td></td></tr><tr><th>Phaloriinae</th><td></td><td><i>Phaloria</i> sp.</td><td>L. Desutter</td><td>♂</td><td>MNHN-EO-ENSIF3078</td><td>Philippines</td><td></td></tr><tr><th colspan="8">GRYLLIDAE</th></tr><tr><th>Eneopterinae</th><td>Eneopterini</td><td><i>Eneoptera guyanensis</i> Chopard, 1931</td><td>L. Desutter</td><td>♂</td><td>MNHN-EO-ENSIF9766</td><td>French Guiana</td><td></td></tr><tr><th></th><td>Lebinthini</td><td><i>Ligypterus fuscus</i> Chopard, 1920</td><td>L. Desutter</td><td>♂</td><td>MNHN-EO-ENSIF9767</td><td>French Guiana</td><td></td></tr><tr><th></th><td>Lebinthini</td><td><i>Agnotecous</i> sp.</td><td>T. Robillard</td><td>♂</td><td>MNHN-EO-ENSIF9937</td><td>New Caledonia</td><td></td></tr><tr><th></th><td>Nisitrini</td><td><i>Nisitrus vittatus</i> (Haan, 1844)</td><td>T. Robillard</td><td>♂</td><td>MNHN-EO-ENSIF9938</td><td>Laboratory strain</td><td></td></tr><tr><th>Pentacentrinae</th><td>Pentacentrini</td><td><i>Pentacentrodes</i> sp.</td><td>L. Desutter</td><td>♂</td><td>MNHN-EO-ENSIF9776</td><td>Madagascar</td><td></td></tr><tr><th>Gryllinae</th><td>Gryllini</td><td rowspan="2"><i>Brachytrupes</i> (Drury, 1773) <i>membranaceus</i></td><td rowspan="2">L. Desutter</td><td rowspan="2">♂/♀</td><td rowspan="2">MNHN-EO-ENSIF9769/ MNHN-EO-ENSIF12162</td><td rowspan="2">Republic of Congo/ Guinea</td><td rowspan="2">♂: 2A, B; 4A; S2A / ♀: S4C</td></tr><tr><th></th><td></td></tr><tr><th></th><td></td><td><i>Acheta domesticus</i> (Linnaeus, 1758)</td><td></td><td>♂</td><td>MNHN-EO-ENSIF9777</td><td>Farm strain</td><td></td></tr><tr><th>Landrevinae</th><td>Landrevini</td><td><i>Landreva</i> sp.</td><td>L. Desutter</td><td>♂</td><td>MNHN-EO-ENSIF9775</td><td>India</td><td>5A; S3A</td></tr><tr><th colspan="8">TRIGONIDIIDAE</th></tr><tr><th>Trigonidiinae</th><td>Trigonidiini</td><td><i>Anaxipha</i> sp.</td><td>L. Desutter</td><td>♂</td><td>MNHN-EO-ENSIF9770</td><td>French Guiana</td><td></td></tr><tr><th></th><td></td><td><i>Natula longipennis</i> (Serville, 1838)</td><td></td><td>♂</td><td>MNHN-EO-ENSIF9933</td><td>Indonesia</td><td>3A, B; S1A, B, C</td></tr><tr><th>Nemobiinae</th><td>Nemobiini</td><td>Nemobius sylvestris (Bosc, 1792)</td><td>L. Desutter</td><td>♂</td><td>MNHN-EO-ENSIF9786</td><td>France</td><td>5B; S3B</td></tr></tbody></table>
FIG. 6 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets
FIG. 6. — Hypothesis of primary venation homology of male forewing of †Protogryllidae (A, B) and †Baissogryllidae (C-E): A, †Angarogryllus angaricus (Sharov 1968), PIN 1873-16; B, †Falsipseculum karatavicum (Sharov 1968), PIN 3791/1345; C, †Neosharategia paradoxa Gorochov, 1992, PIN 4270-210a; D, †Baissogryllidae sp., CCNH-293; E, †Anglogryllus lyristes Gorochov et al., 2006, MNEMG 2003.46. Abbreviations: "ha", distally opened harp; "mi", distally opened mirror, others and colour code, see text. Grey dash lines represent folds. Scale bars: 1 mm.
FIG. 9 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets
FIG. 9. — Hypotheses of primary venation homology of forewing of †Liassophyllum caii Gu & Ren, 2012 (CNU-ORT-NN2009008, †Tuphelidae). Modified from Gu et al. (2012). Abbreviations and colour code: see text. Scale bar: 5 mm.
FIG. 3 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets
FIG. 3. — Hypothesis of primary homology of venation of male Grylloidea: A, Natula longipennis (Serville, 1838) (MNHN-EO-ENSIF9933, Trigonidiidae); B, Lerneca fuscipennis (Saussure, 1874) (MNHN-EO-ENSIF9780, Phalangopsidae). Abbreviations and colour code: see text. Scale bars:1 mm.
FIG. 4 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets
FIG. 4. — Hypothesis of primary homology of venation of male Grylloidea: A, Brachytrupes membranaceus (Drury, 1773) (MNHN-EO-ENSIF9769, Gryllidae); B, Phyllogryllus sp. (MNHN-EO-ENSIF9768, Oecanthidae). Abbreviations and colour code: see text. Grey dash lines represent folds. Scale bars: 5 mm.
FIG. 2 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets
FIG. 2. — Main fields (A, C) and functional structures (B, D) of a male grylloid forewing (A, B: Brachytrupes membranaceus (Drury, 1773), MNHN-EO-ENSIF9769) and a male gryllotalpid forewing (C, D: Scapteriscus sp., MNHN-EO-ENSIF3068). Abbreviations: lc, lanceolate cell; ha, harp; mi, mirror. Scale bars: 5 mm.
FIG. S1 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets
FIG. S1. — Forewings of male Grylloidea with hypothesis of venation: A, B, Natula longipennis (Serville, 1838) (MNHN-EO-ENSIF9933, Trigonidiidae); C, Anaxipha sp. (MNHN-EO-ENSIF9770, Trigonidiidae);D, Lerneca fuscipennis (Saussure,1874) (MNHN-EO-ENSIF9780, Phalangopsidae).Abbreviations:see text. Scale bars:1 mm.
DATA SUPPORTING RESEARCH ON THE DEVELOPMENT OF PALEONTOLOGY IN BRAZIL (NETWORK VISUALIZATIONS)
<p>The documents made available present the data set that was processed in Lucas George Wendt's dissertation, presented in 2024 in the Postgraduate Program in Information Science (PPGCIN) of the Federal University of Rio Grande do Sul (UFRGS). The study is entitled: Brazilian Paleontology: a scientometric analysis based on the Lattes Curriculum. The abstract is as follows. This research sought to carry out a scientometric analysis of Paleontology in Brazil based on data collected in the Lattes Curriculum. The general objective of this dissertation is to analyze the scientific field of Paleontology diachronically and through a scientometric study - which will be explained based on the personal information of the researchers collected in their profiles and the scientific literature produced and registered in the Lattes Curriculum of the Lattes Platform. The literature review presented the concepts of Information Science, the area that, in this study, seeks to understand Paleontology through its research instruments; Scientific Communication, the main subject analyzed in this study; Metric Information Studies, the theoretical-methodological framework used in this research; Scientometrics, the theoretical scope used to understand in greater depth the constitution of the field of national Paleontology. Finally, references were also presented that help in the understanding of Paleontology in its national, South American, North American and European contexts. The research used a mixed approach of qualitative and quantitative elements. The data were generated from the CVs of researchers registered on the Lattes Platform, collected using the Brapci Bibliometric Tools tool and analyzed in specific software for metric analysis. To achieve the research objectives, data from 1,465 researcher profiles were analyzed. Regarding the full articles published in journals, 43,333 articles were considered valid. Regarding the keywords of the articles, 91,922 keywords were analyzed for word clouds and 84,771 for relationship networks. Of the academic orientations, 1,182 profiles generated 51,400 valid orientations. The aspect of the current employment relationship had 1,256 profiles considered. Regarding academic backgrounds, 1,465 profiles generated 4,556 academic backgrounds analyzed. The main contribution of this study is the realization of an unprecedented mapping of the panorama of Paleontology in Brazil, since there are no other studies that establish the same relationships that this research sought to establish. Regarding the results, based on the data collected and analyzed, the general metric indicators linked to the scientific production associated with Brazilian Paleontology were presented based on the information collected in the Lattes Curriculum; the directions of research in Paleontology that currently constitute this field in Brazil were mapped, as well as their thematic associations with other fields of knowledge; the training of PhD researchers who work with Paleontology or who have their production associated with Paleontology in terms of their academic training was characterized; and where the scientific knowledge in Paleontology or associated with Paleontology is produced was identified. The results of this study are relevant to understanding Brazilian Paleontology, highlighting its national orientation in fossil studies, doctoral training in local institutions and predominant activity in national organizations. These elements are important to consolidate Brazilian paleontological science globally. Regarding interdisciplinary relations, a clear proximity between Paleontology and Geosciences is observed, influenced by the history and current dynamics of the field. The study is available in full at this link: https://lume.ufrgs.br/handle/10183/278682.</p>
FIGURE 8 in Description of contents of unopened bamboo corsets and crates from Quarry Ig/WJ of the Tendaguru locality (Late Jurassic, Tanzania, East Africa) as revealed by medical CT data and the potential of this data under paleontological and historical aspects
FIGURE 8. Examples of bone elements from sauropod dinosaurs found in the bamboo corsets, link to corresponding movies. A) "Ig 230", cervical rib of Giraffatitan brancai, and cluster of vertebrae and bone fragments of Dysalotosaurus; B) "Ig 281", presumable dorsal vertebral fragments and pneumatic transverse process of a sauropod (this bamboo corset contains also a dentary remain of Dysalotosaurus); C) "Ig 310, 311, 312, 313, 314", pneumatic transverse process of dorsal vertebra; D) "Ig 498", neural arch with clearly visible hyposphene and broken neural spine of titanosauriform sauropod. Close-up of visualization of isolated MtII of Giraffatitan, E) in dorsal view F) in plantar view. Scale bar in A-D is 100 mm, in E-F it is 50 mm. Abbreviations: bf, bone fragment; ccost, corpus of cervical rib (of Giraffatitan); df, dentary fragment (of Dysalotosaurus); hypo, hyposphene; mt, metatarsal; na, neural arch; nsp, neural spine; prcost, caudal process of cervical rib (of Giraffatitan); postzyg, postzygapophysis; prtrans, transverse process of vertebra; tib,tibia; vc, vertebral centrum; vf, vertebral fragment. Videos of A) to D) available at the PE You Tube channel (https://www.youtube.com/channel/UCF6IBDiGbut- DrVada60Izyg)
FIGURE 6 in Description of contents of unopened bamboo corsets and crates from Quarry Ig/WJ of the Tendaguru locality (Late Jurassic, Tanzania, East Africa) as revealed by medical CT data and the potential of this data under paleontological and historical aspects
FIGURE 6. Examples of bone elements from Dysalotosaurus lettowvorbecki as found in the bamboo corsets, link to corresponding movies. A) "Ig 189, 211, 213", bamboo corset with dentary fragments, dorsal rib shaft, tibia remains, a proximal fibula and some other bone fragments; B) "Ig 401, 415, 416, 417, 472, 475", bamboo corset with well-preserved ilium, proximal fibula, at least two metatarsals and other long bone fragments, as well as a presumed MtII of Giraffatitan brancai in 2 parts; C) "Ig 343, 346, 354, 359, 366, 383", bamboo corset with femur in 3 parts, fragments of ilium and some bone fragments; D) "Ig 335, 336, 338, 368", bamboo corset with 1 humerus, 1 femur, tibia and fibula as proximal parts and other bone fragments; E) "Ig 537, 540, 547, 549, 562", bamboo corset with vertebral centra, 2 isolated neural arches, a coracoid, a distal femur, a metatarsal and other bone fragments; F) "Ig 522, 527, 528, 539, 543, 544", bamboo corset with tibia and fibula, ulna and other bone fragments. Scale bar is 50 mm. Abbreviations: cor, coracoid; df, dentary fragment; dori, dorsal rib; fe, femur; fib, fibula; hu, humerus; ili, ilium; isc, ischium; MtII, second metatarsal of Giraffatitan; mt, metatarsal (of Dysalotosaurus); nar, neural arch; tib, tibia; uln, ulna; vc, vertebral centrum. Videos of A) to F) available at the PE You Tube channel (https://www.youtube.com/channel/UCF6IBDiGbut- DrVada60Izyg)
FIGURE 5. Diagrams showing A in Description of contents of unopened bamboo corsets and crates from Quarry Ig/WJ of the Tendaguru locality (Late Jurassic, Tanzania, East Africa) as revealed by medical CT data and the potential of this data under paleontological and historical aspects
FIGURE 5. Diagrams showing A) the distribution of clay jackets, unprepared bones and tin cans in the bamboo corsets and crates, B) Frequency of different bone elements of Dysalotosaurus lettowvorbecki in the bamboo corsets and crates. The unidentified bone fragments of Dysalotosaurus are not incorporated in this count. Isolated vertebral centra have been counted without determination of their corresponding body region (i.e., cervical, dorsal, sacral, or caudal).
FIGURE 4 in Description of contents of unopened bamboo corsets and crates from Quarry Ig/WJ of the Tendaguru locality (Late Jurassic, Tanzania, East Africa) as revealed by medical CT data and the potential of this data under paleontological and historical aspects
FIGURE 4. Packing types of fossil specimens as visible in the CT images A) "Ig 420, 439, 453, 512", longitudinal section (MIP mode and CT-pulmonary filters set) showing wrapping of specimens in savanna grass, B) "Ig88" cross-section showing wrapping of fossils in savanna grass and tight stuffing of bamboo corsets, C) "Ig291, 291", longitudinal section of the typical clay jackets, showing a femur of Dysalotosaurus in pieces with protection cover of clay, D) "Ig281", partial longitudinal section showing clay jackets and single bone fragments with and without sediment, E) "Ig 122, 124, 266, 267, 269, 270, 272, 276", longitudinal section showing clusters of vertebrae and bone fragments in the bamboo corset, F) "Ig_2011_4", crate with two large sediment slabs with fossil bones, G) "Ig_2011_1", crate with bamboo stalks filled with fossil bones and bones wrapped in savanna grass, H) "Ig_NN6", bamboo corset in longitudinal section (MIP mode) showing tin cans and bone cluster in between (see also Figure 4C-D), I) "Ig 330, 339, 347, 349 350, 351, 352, 356, 360, 346, 366", bamboo corset in longitudinal section (MIP mode) showing several tin cans and some additional loose bones. Scale bar is 50 mm. Abbreviations: bb, bamboo stalk; bf, bone fragment; cl, clay cover of bone; clj, clay jacket; df, dentary fragment; dife, distal femur; sed, sediment; sgb, savanna grass bundle; vc, vertebral centrum.
ScienceDex guides
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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.