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.
15,519
datasets available to search
ShareScore release 0.9.0
Dataset results
15,519 results for “r”
Figure 2 from: Deng L-S, Kang R, Zeng N-K, Yu W-J, Chang C, Xu F, Deng W-Q, Qi L-L, Zhou Y-L, Fan Y-G (2021) Two new Inosperma (Inocybaceae) species with unexpected muscarine contents from tropical China. MycoKeys 85: 87-108. https://doi.org/10.3897/mycokeys.85.71957
Figure 2 Basidiomata of Inosperma muscariuma–e basidiomata f–h rimose to rimulose pileus i lamellae j–k lamellae edge l–m stipe surface. a–b, d, f–g, i–m FHMU3162 (holotype) c, e FYG6092 (FHMU3163) h FYG6093 (FHMU3164). Scale bars: 10 mm (a–m). Photos by Y.-G. Fan.
Figure 3 from: Sultana R, Sanam S, Kumar S, Shamsudeen R SM, Soomro F (2021) A review of Gryllidae (Grylloidea) with the description of one new species and four new distribution records from the Sindh Province, Pakistan. ZooKeys 1078: 1-33. https://doi.org/10.3897/zookeys.1078.69850
Figure 3 Male and female head dorsal view of Gryllidae species, subfamily Gryllinae: 11 T. (Brachyteleogryllus) commodus ♀, 12 Modicogryllus sindhensis sp. nov. ♀,13 Svercus palmetorum ♀, 14 Miogryllus itaquiensis ♀, 15 Callogryllus saeedi ♀, 16 C. ovilongus ♀, 17 C. bilineatus ♀, 18 Lepidogryllus siamensis ♀. Subfamily Oecanthinae: 19 Oecanthus fultoni ♀. Abbreviations: D, dorsal, L, lateral. Scale bars: 2 mm.
Figure 4 from: Sultana R, Sanam S, Kumar S, Shamsudeen R SM, Soomro F (2021) A review of Gryllidae (Grylloidea) with the description of one new species and four new distribution records from the Sindh Province, Pakistan. ZooKeys 1078: 1-33. https://doi.org/10.3897/zookeys.1078.69850
Figure 4 Male and female pronotum dorsal view of Gryllidae species, subfamily Gryllinae: 1, 2 Acheta domesticus ♂♀, 3 A. hispanicus ♂, 4, 5 Gryllus (Gryllus) bimaculatus ♂♀, 6 G. (Gryllus) campestris ♀, 7 G. septentrionalis ♀, 8 Gryllodes sigillatus ♂, 9 Gryllodes supplicans ♀, 10 Teleogryllus (Brachyteleogryllus) occipitalis ♀. Abbreviations: D, dorsal, L, lateral. Scale bars: 2 mm.
Figure 2 from: Liu D-H, Xu X-M, He Y, Liu Q-R (2021) A new combination in Pseudolappula (Boraginaceae, Rochelieae) based on morphological, molecular and palynological evidence. PhytoKeys 187: 77-92. https://doi.org/10.3897/phytokeys.187.75346
Figure 2 Maximum Likelihood tree of subtribe Eritrichiinae inferred from ITS + trnL-F. The tree topology was constructed using RAxML. Bootstrap values and Bayesian posterior probabilities are indicated above branches. Note that the Lappula occultata (Huang et al. 2013) is a misidentified voucher from previous studies (Huang et al. 2013).
Figure 1 from: Liu D-H, Xu X-M, He Y, Liu Q-R (2021) A new combination in Pseudolappula (Boraginaceae, Rochelieae) based on morphological, molecular and palynological evidence. PhytoKeys 187: 77-92. https://doi.org/10.3897/phytokeys.187.75346
Figure 1 Nutlet morphology of Pseudolappula and LappulaA–DPseudolappula sinaicaA fruit lateral view B fruit polar view (growth direction of nutlets indicated by arrows) C nutlet abaxial view D nutlet adaxial view E–HLappula occultataE fruit lateral view F fruit polar view (arrangement of nutlets indicated by cross lines) G nutlet abaxial view H nutlet adaxial view I–LLappula patulaI fruit lateral view J fruit polar view (arrangement of nutlets indicated by cross lines) K nutlet abaxial view L nutlet adaxial view M adaxial keel of P. sinaica (adaxial view) N adaxial keel of L. occultata (lateral view) O attachment scar of Lappula balchaschensisP attachment scar of Lappula brachycentra. Scale bars: 1 mm.
Figure 1 from: Wilf P, Wing SL, Meyer HW, Rose JA, Saha R, Serre T, Cúneo NR, Donovan MP, Erwin DM, Gandolfo MA, González-Akre E, Herrera F, Hu S, Iglesias A, Johnson KR, Karim TS, Zou X (2021) An image dataset of cleared, x-rayed, and fossil leaves vetted to plant family for human and machine learning. PhytoKeys 187: 93-128. https://doi.org/10.3897/phytokeys.187.72350
Figure 1 Selected image pairs of confamilial extant and fossil (see Appendix 1) leaves from the dataset ABatesia floribunda Spruce ex. Benth. (Fabaceae), NCLC-W 6417, showing typical layout of a cleared-leaf slide with original annotations (other examples are cropped in this figure); source voucher Froes 12074, DS 291771 (at CAS), Amazonas, Brazil BFabaceae sp. CJ1, SGC-ICP-10173; Cerrejón mine, middle-late Paleocene of Guajira Peninsula, Colombia CCrataegus viridis L. (Rosaceae), NCLC-W 11951b; H. Meyer s/n (collected 1974, no other voucher), cultivated, California, USA DCrataegus copeana (Rosaceae), UCMP 3610; Florissant, late Eocene of Colorado, USA; H. Meyer photograph number 0420 ETetracentron sinense Oliv. (Trochodendraceae), S. Wing negative 71-002; E.H. Wilson 659, US 599036, Szechuan, China FZiziphoides flabellum (Trochodendraceae), USNM 560134; Mexican Hat, early Paleocene of Montana, USA GQuercus prinus L. (Fagaceae), NCLC-W 6137; H. Foster 8223, US 1730249, Florida, USA HFagopsis longifolia (Fagaceae), FLFO 003432A; Florissant, late Eocene of Colorado, USA IEucalyptus astringens (Maiden) Maiden (Myrtaceae), NCLC-W 10489; J.H. Maiden (9 November 1909), Western Australia, UC 437518 JEucalyptus frenguelliana (Myrtaceae), MPEF-Pb 2344; Laguna del Hunco, early Eocene of Chubut, Argentina KCercidiphyllum obtritum (Cercidiphyllaceae), DMNH 25061; Republic, early Eocene of Washington, USA LCercidiphyllum japonicum Siebold & Zucc. ex J.J.Hoffm. & J.H.Schult.bis (Cercidiphyllaceae), Axelrod cleared leaf 166; UCMP (no other voucher) MPlatanus racemosa Nutt. (Platanaceae), NCLC-H 6631; Handel s/n (collected 1985, no other voucher), California, USA NErlingdorfia montana (compound-leaved Platanaceae), DMNH 7642; Hell Creek Formation, Late Cretaceous of North Dakota, USA. Scale bars: centimeters as labeled (A, B, L, M); 1 cm when not labeled (C–K, N).
Figure 3 from: Liu D-H, Xu X-M, He Y, Liu Q-R (2021) A new combination in Pseudolappula (Boraginaceae, Rochelieae) based on morphological, molecular and palynological evidence. PhytoKeys 187: 77-92. https://doi.org/10.3897/phytokeys.187.75346
Figure 3 Scanning electron micrographs. A, BPseudolappula sinaicaC, DLappula occultataE, FL. shanhsiensisG, HL. redowskiiI, JL. macranthaK, LL. tianschanicaM, NRochelia bungeO, PPseudoheterocaryum rigidum. Scale bars: 5 μm.
Supplementary material 2 from: Boukhdoud L, Saliba C, Parker LD, McInerney NR, Kahale R, Saliba I, Maldonado JE, Kharrat MBD (2021) Using DNA metabarcoding to decipher the diet plant component of mammals from the Eastern Mediterranean region. Metabarcoding and Metagenomics 5: e70107. https://doi.org/10.3897/mbmg.5.70107
Appendix 2
Supplementary material 1 from: Boukhdoud L, Saliba C, Parker LD, McInerney NR, Kahale R, Saliba I, Maldonado JE, Kharrat MBD (2021) Using DNA metabarcoding to decipher the diet plant component of mammals from the Eastern Mediterranean region. Metabarcoding and Metagenomics 5: e70107. https://doi.org/10.3897/mbmg.5.70107
Appendix 1
Figure 1 from: Catania R, Nobile V, Bella S (2021) The species of Eucera Scopoli, subgenus Tetralonia Spinola from Sardinia (Italy) with new records and E. alticincta gennargentui ssp. n. (Hymenoptera, Apidae). Journal of Hymenoptera Research 88: 1-16. https://doi.org/10.3897/jhr.88.70819
Figure 1 Sardinia and Gennargentu Massif, locality of Bruncu Spina, 1540 m a.s.l., the site of the samplings of Eucera gennargentui sp. nov.
Figure 4 from: Catania R, Nobile V, Bella S (2021) The species of Eucera Scopoli, subgenus Tetralonia Spinola from Sardinia (Italy) with new records and E. alticincta gennargentui ssp. n. (Hymenoptera, Apidae). Journal of Hymenoptera Research 88: 1-16. https://doi.org/10.3897/jhr.88.70819
Figure 4 Eucera gennargentui sp. nov., male (A-E) A head, anterior view B habitus, lateral view C dorsal view D mesosoma, dorsal view E metasoma, dorsal view. (Photos by R. Catania).
Figure 7 from: Catania R, Nobile V, Bella S (2021) The species of Eucera Scopoli, subgenus Tetralonia Spinola from Sardinia (Italy) with new records and E. alticincta gennargentui ssp. n. (Hymenoptera, Apidae). Journal of Hymenoptera Research 88: 1-16. https://doi.org/10.3897/jhr.88.70819
Figure 7 Neighbor-Joining tree showing relationships among Eucera gennargentui sp. nov., and Eucera (Tetralonia) species with Habropoda tarsata used as the outgroup.
Figure 3 from: Catania R, Nobile V, Bella S (2021) The species of Eucera Scopoli, subgenus Tetralonia Spinola from Sardinia (Italy) with new records and E. alticincta gennargentui ssp. n. (Hymenoptera, Apidae). Journal of Hymenoptera Research 88: 1-16. https://doi.org/10.3897/jhr.88.70819
Figure 3 Eucera gennargentui sp. nov., female (A-E) A head, anterior view B habitus, lateral view C dorsal view D mesosoma, dorsal view E metasoma, dorsal view. (Photos by R. Catania).
Figure 5 from: Catania R, Nobile V, Bella S (2021) The species of Eucera Scopoli, subgenus Tetralonia Spinola from Sardinia (Italy) with new records and E. alticincta gennargentui ssp. n. (Hymenoptera, Apidae). Journal of Hymenoptera Research 88: 1-16. https://doi.org/10.3897/jhr.88.70819
Figure 5 Eucera gennargentui sp. nov., genitalia and hidden sterna (A-F) A S6 ventral view B S7 ventral view C S8 ventral view D genitalia, dorsal view E genitalia, lateral view F vision of gonostylus and posterodorsal projection of gonocoxa (Photos by R. Catania).
Figure 6 from: Catania R, Nobile V, Bella S (2021) The species of Eucera Scopoli, subgenus Tetralonia Spinola from Sardinia (Italy) with new records and E. alticincta gennargentui ssp. n. (Hymenoptera, Apidae). Journal of Hymenoptera Research 88: 1-16. https://doi.org/10.3897/jhr.88.70819
Figure 6 Female of Eucera gennargentui sp. nov. Sardinia, Gennargentu Massif, locality of Bruncu Spina (Photos by P. Niolu - R. Catania).
Fig. 18. Rhachomyces spp. A–B. R in Laboulbeniomycetes (Fungi, Ascomycota) of Denmark
Fig. 18. Rhachomyces spp. A–B. R. philonthinus Thaxt. Mature thalli. In B, the lateral branch from the primary axis (a diagnostic character) is labelled (arrow). – C–D. R. pilosellus (C.P.Robin) Thaxt. Mature thalli with labelled blackened diagonal strip traversing cells I and II (arrows). – E–F. R. spinosus Santam. & Cuesta-Segura. Mature thalli. In E, primary septum (a) and spinous original spore apex (sx) are labelled. Scale bars: 50 µm. Photographs from slides ZMUC C-F-122681 (A), ZMUC C-F-122685 (B), ZMUC C-F-123833 (C–D), ZMUC C-F-123296 (E), ZMUC C-F-123062 (F).
Figure 3 from: Datry T, Allen D, Argelich R, Barquin J, Bonada N, Boulton A, Branger F, Cai Y, Cañedo-Argüelles M, Cid N, Csabai Z, Dallimer M, de Araújo JC, Declerck S, Dekker T, Döll P, Encalada A, Forcellini M, Foulquier A, Heino J, Jabot F, Keszler P, Kopperoinen L, Kralisch S, Künne A, Lamouroux N, Lauvernet C, Lehtoranta V, Loskotová B, Marcé R, Martin Ortega J, Matauschek C, Miliša M, Mogyorósi S, Moya N, Müller Schmied H, Munné A, Munoz F, Mykrä H, Pal I, Paloniemi R, Pařil P, Pengal P, Pernecker B, Polášek M, Rezende C, Sabater S, Sarremejane R, Schmidt G, Senerpont Domis L, Singer G, Suárez E, Talluto M, Teurlincx S, Trautmann T, Truchy A, Tyllianakis E, Väisänen S, Varumo L, Vidal J-P, Vilmi A, Vinyoles D (2021) Securing Biodiversity, Functional Integrity, and Ecosystem Services in Drying River Networks (DRYvER). Research Ideas and Outcomes 7: e77750. https://doi.org/10.3897/rio.7.e77750
Figure 3 The DRYvER three-step workflow embedded within 7 Work Packages (WP) and the four main attributes of the DRYvER consortium (red ovals).
Figure 2 from: Datry T, Allen D, Argelich R, Barquin J, Bonada N, Boulton A, Branger F, Cai Y, Cañedo-Argüelles M, Cid N, Csabai Z, Dallimer M, de Araújo JC, Declerck S, Dekker T, Döll P, Encalada A, Forcellini M, Foulquier A, Heino J, Jabot F, Keszler P, Kopperoinen L, Kralisch S, Künne A, Lamouroux N, Lauvernet C, Lehtoranta V, Loskotová B, Marcé R, Martin Ortega J, Matauschek C, Miliša M, Mogyorósi S, Moya N, Müller Schmied H, Munné A, Munoz F, Mykrä H, Pal I, Paloniemi R, Pařil P, Pengal P, Pernecker B, Polášek M, Rezende C, Sabater S, Sarremejane R, Schmidt G, Senerpont Domis L, Singer G, Suárez E, Talluto M, Teurlincx S, Trautmann T, Truchy A, Tyllianakis E, Väisänen S, Varumo L, Vidal J-P, Vilmi A, Vinyoles D (2021) Securing Biodiversity, Functional Integrity, and Ecosystem Services in Drying River Networks (DRYvER). Research Ideas and Outcomes 7: e77750. https://doi.org/10.3897/rio.7.e77750
Figure 2 It shows how DRYvER will use this cyclic model as a structured loop embedded in a meta-system perspective to guide adaptive management of DRNs. DRYvER will translate climate projections into changes in flow intermittence patterns at multiple scales, including that of the strategically-selected focal DRNs. This physical setting will then be used to implement a dynamic meta-system perspective to understand the cascading changes in biodiversity, ecosystem functions and ecosystem services. This knowledge will be integrated to develop a multi-criteria decision framework combining scientific, management, socio-economic, legislative barriers and leverages to promote an adaptive management of DRNs.
Figure 4 from: Datry T, Allen D, Argelich R, Barquin J, Bonada N, Boulton A, Branger F, Cai Y, Cañedo-Argüelles M, Cid N, Csabai Z, Dallimer M, de Araújo JC, Declerck S, Dekker T, Döll P, Encalada A, Forcellini M, Foulquier A, Heino J, Jabot F, Keszler P, Kopperoinen L, Kralisch S, Künne A, Lamouroux N, Lauvernet C, Lehtoranta V, Loskotová B, Marcé R, Martin Ortega J, Matauschek C, Miliša M, Mogyorósi S, Moya N, Müller Schmied H, Munné A, Munoz F, Mykrä H, Pal I, Paloniemi R, Pařil P, Pengal P, Pernecker B, Polášek M, Rezende C, Sabater S, Sarremejane R, Schmidt G, Senerpont Domis L, Singer G, Suárez E, Talluto M, Teurlincx S, Trautmann T, Truchy A, Tyllianakis E, Väisänen S, Varumo L, Vidal J-P, Vilmi A, Vinyoles D (2021) Securing Biodiversity, Functional Integrity, and Ecosystem Services in Drying River Networks (DRYvER). Research Ideas and Outcomes 7: e77750. https://doi.org/10.3897/rio.7.e77750
Figure 4 DRYvER focal DRNs located in highly contrasted EU and CELAC biogeographic and climatic settings (red points), chosen to span the expected natural variability of drying processes and associated DRN responses.Mediterranean ecoregion: the Genal network, in Andalucía (Spain, Mediterranean climate), a dry region heavily impacted by climate change, where most rivers are already affected by drying (contact partner: UB);Alpine ecoregion: the Albarine network, in the Southern Jura (France, temperate climate), a region mildly impacted by climate change (the Albarine network is part of a national LTER project and monitored since 2006) (contact partner: INRAE);Continental ecoregion: the Velička network, in Morava (Czech Republic, continental climate), a region heavily impacted by climate change where many perennial rivers are shifting towards intermittent flow (contact partner: MU);Balkanic ecoregion: the Krka network, in the Dinaric Karst (Croatia, Mediterranean climate), a region where most rivers are already drying and heavily impacted by climate change (contact partner: UZ);Pannonian ecoregion: the Bükkösdi-víz network, in the Mecsek (Hungary, continental climate), a region moderately impacted by climate change, where DRNs are becoming common (contact partner: UP);Boreal ecoregion: the Vantaanjoki network, Helsinki-Uusimaa Region (Finland, boreal climate), region moderately impacted by climate change, where flow intermittence is currently rare (contact partner: SYKE);Pacific Lowlands: the Cube network, in the Andean-Choco region (Ecuador, tropical climate), a region where drying is very seasonal and increasing in duration and frequency (contact partner: USFQ);Central High Andes ecoregion: the Rio Chico network in the Sucre region (Bolivia, semi-arid climate), a dry area prone to desertification where political conflicts emerge due to water scarcity (contact partner: USFX);Caatinga ecoregion: the Jaguaribe network, in the Northeast Semiarid region (Brazil, semi-arid climate), the driest region in Brazil, already heavily impacted by climate change (contact partner: UFC).
Figure 1 from: Datry T, Allen D, Argelich R, Barquin J, Bonada N, Boulton A, Branger F, Cai Y, Cañedo-Argüelles M, Cid N, Csabai Z, Dallimer M, de Araújo JC, Declerck S, Dekker T, Döll P, Encalada A, Forcellini M, Foulquier A, Heino J, Jabot F, Keszler P, Kopperoinen L, Kralisch S, Künne A, Lamouroux N, Lauvernet C, Lehtoranta V, Loskotová B, Marcé R, Martin Ortega J, Matauschek C, Miliša M, Mogyorósi S, Moya N, Müller Schmied H, Munné A, Munoz F, Mykrä H, Pal I, Paloniemi R, Pařil P, Pengal P, Pernecker B, Polášek M, Rezende C, Sabater S, Sarremejane R, Schmidt G, Senerpont Domis L, Singer G, Suárez E, Talluto M, Teurlincx S, Trautmann T, Truchy A, Tyllianakis E, Väisänen S, Varumo L, Vidal J-P, Vilmi A, Vinyoles D (2021) Securing Biodiversity, Functional Integrity, and Ecosystem Services in Drying River Networks (DRYvER). Research Ideas and Outcomes 7: e77750. https://doi.org/10.3897/rio.7.e77750
Figure 1 Phases of flowing and drying alternate annually in the naturally intermittent Albarine River (France), a focal DRN of DRYvER. About half of EU's river channels now flow intermittently and this fraction is increasing. Photos: T. Datry.
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.