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980 results for “Coping”
Fig. 2. Apostolepis albicollarisLema, 2002 in Unveiling an enigma from the Cerrado: taxonomic revision of two sympatric species of Apostolepis Cope, 1862 (Dipsadidae: Xenodontinae: Elapomorphini) from central Brazil
Fig. 2. Apostolepis albicollarisLema, 2002, coloration in life and polymorphism. Holotype of A. albicollaris from Brasília, Distrito Federal, Brazil (MCP 8355) (top). Holotype of Apostolepis cerradoensis Lema, 2003 from Minaçu, Goiás, Brazil (MCP 15219) (bottom). Drawings: Arthur Tiutenko.
Helictotrichon recurvatum (Swallen) Cope & Ryves (BR0000011470090)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Fig. 3 in New distribution records and conservation status of Atelopus seminiferus Cope, 1874: A Critically Endangered harlequin frog from northern Peru
Fig. 3. Updated distribution map of Atelopus seminiferus. Black dots indicate new localities reported in this study. Light green area corresponds the estimated Extent of Occurrence (ca. 2,520 km2) based on the new records presented here and the previously known localities. Numbers correspond to labels in Table 1. Map by Juan C. Cusi.
Fig. 3 in New distribution records and conservation status of Atelopus seminiferus Cope, 1874: A Critically Endangered harlequin frog from northern Peru
Fig. 3. Dorsal and ventral views of the holotype of Atelopus seminifeus (ANSP 11383), deposited in the herpetological collection at the Academy of Natural Sciences of Drexel University, Philadelphia. Photos courtesy of Ned Gilmore.
Fig. 2 in New distribution records and conservation status of Atelopus seminiferus Cope, 1874: A Critically Endangered harlequin frog from northern Peru
Fig. 2. (A) A pair of Atelopus seminiferus in amplexus, found between El Carmen and La Esperanza [not collected]. Photo by Fredi Sangama and Florencio León. (B) Dorsal coloration pattern of a female MUSM 33328. (C) Ventral coloration pattern in a male MUSM 33327. (D) Ventral coloration pattern in a female MUSM JCM H-24. (D) El Carmen village in Alto Mayo Protected Forest, Rioja province, San Martin (E). Photos B‒E by Juan C. Cusi.
Fig. 1 in New distribution records and conservation status of Atelopus seminiferus Cope, 1874: A Critically Endangered harlequin frog from northern Peru
Fig. 1. Distribution of Atelopus seminiferus in the Mayo River basin, San Martin, Peru. Yellow polygon corresponds to geographic range estimated by IUCN. Compare with Fig. 3, which shows proposed new polygon based on results from this study. Map by Juan C. Cusi.
Plate 34. Sceloporus malachiticus Cope, 1864 in The endemic herpetofauna of Central America: a casualty of anthropocentrism
Plate 34. Sceloporus malachiticus Cope, 1864. The Green Spiny Lizard is a priority three species with an EVS of 10, distributed from "El Salvador and Honduras across Nicaragua and Costa Rica to Panama" (Köhler 2008: 152). This individual was encountered in Cerro de la Muerte, in the province of San José, Costa Rica. Photo by Víctor Acosta-Chaves.
Plate 39. Lachesis stenophrys Cope, 1875 in The endemic herpetofauna of Central America: a casualty of anthropocentrism
Plate 39. Lachesis stenophrys Cope, 1875. The Central American Bushmaster is a priority two species with an EVS of 17, distributed from "southeastern Nicaragua to central Panama" (Köhler 2008: 330). This individual came from Parque Nacional Braulio Carrillo, in the province of Heredia, Costa Rica. Photo by César Barrio-Amorós.
Fig. 13 in Redescription of Astyanax obscurus (Hensel, 1870) and A. laticeps (Cope, 1894) (Teleostei: Characidae): two valid freshwater species originally described from rivers of Southern Brazil
Fig. 13. Projection of individual scores in the space of first and second Principal Component axis for the populations of females of Astyanax laticeps.
Fig. 12 in Redescription of Astyanax obscurus (Hensel, 1870) and A. laticeps (Cope, 1894) (Teleostei: Characidae): two valid freshwater species originally described from rivers of Southern Brazil
Fig. 12. Projection of individual scores in the space of first and third Principal Component axis for the populations of males and females of Astyanax laticeps.
Fig. 10 in Redescription of Astyanax obscurus (Hensel, 1870) and A. laticeps (Cope, 1894) (Teleostei: Characidae): two valid freshwater species originally described from rivers of Southern Brazil
Fig. 10. Tukey box plots of number of scales around the caudal peduncle in Astyanax laticeps populations by river drainage from south to north. Mean represented by thick vertical bar and 25th and 75th percetiles as lateral borders of box plots.
Fig. 9 in Redescription of Astyanax obscurus (Hensel, 1870) and A. laticeps (Cope, 1894) (Teleostei: Characidae): two valid freshwater species originally described from rivers of Southern Brazil
Fig. 9. Tukey box plots of number of perforated scales of lateral line in Astyanax laticeps populations by river drainage from south to north. Mean represented by thick vertical bar and 25th and 75th percetiles as lateral borders of box plots.
Fig. 8. Astyanax laticeps, UFRGS 4576 in Redescription of Astyanax obscurus (Hensel, 1870) and A. laticeps (Cope, 1894) (Teleostei: Characidae): two valid freshwater species originally described from rivers of Southern Brazil
Fig. 8. Astyanax laticeps, UFRGS 4576, male, 49.2 mm SL. SEM image of upper and lower jaws, right side. Scale bar = 1 mm.
Fig. 7. Astyanax laticeps, MCP 35425, 61.2 in Redescription of Astyanax obscurus (Hensel, 1870) and A. laticeps (Cope, 1894) (Teleostei: Characidae): two valid freshwater species originally described from rivers of Southern Brazil
Fig. 7. Astyanax laticeps, MCP 35425, 61.2 mm SL, tributary of rio Ivaí, rio Jacuí drainage, Júlio de Castilhos, Rio Grande do Sul, Brazil.
Fig. 5 in Redescription of Astyanax obscurus (Hensel, 1870) and A. laticeps (Cope, 1894) (Teleostei: Characidae): two valid freshwater species originally described from rivers of Southern Brazil
Fig. 5. Map of southern Brazil and Uruguay, showing the distribution of examined material of Astyanax obscurus (circles), and Astyanax laticeps (squares). Some symbols represent more than one lot or locality.
Fig. 3. Astyanax obscurus, MCP 26125, 65.5 in Redescription of Astyanax obscurus (Hensel, 1870) and A. laticeps (Cope, 1894) (Teleostei: Characidae): two valid freshwater species originally described from rivers of Southern Brazil
Fig. 3. Astyanax obscurus, MCP 26125, 65.5 mm SL. SEM image of upper and lower jaws, right side. Scale bar = 2 mm.
Fig. 4 in Redescription of Astyanax obscurus (Hensel, 1870) and A. laticeps (Cope, 1894) (Teleostei: Characidae): two valid freshwater species originally described from rivers of Southern Brazil
Fig. 4. Lateral view of left side of anterior region showing humeral spots of (a) Astyanax obscurus, MCP 26125, 75.6 mm SL, and (b) Astyanax laticeps, MCP 26127, 71.1 mm SL.
Fig. 2. Astyanax obscurus, MCP 40000, 59.2 in Redescription of Astyanax obscurus (Hensel, 1870) and A. laticeps (Cope, 1894) (Teleostei: Characidae): two valid freshwater species originally described from rivers of Southern Brazil
Fig. 2. Astyanax obscurus, MCP 40000, 59.2 mm SL, rio Cadeia above the large waterfalls, Santa Maria do Herval, Rio Grande do Sul, Brazil.
Fig. 1. Astyanax obscurus, ZMB 7478 in Redescription of Astyanax obscurus (Hensel, 1870) and A. laticeps (Cope, 1894) (Teleostei: Characidae): two valid freshwater species originally described from rivers of Southern Brazil
Fig. 1. Astyanax obscurus, ZMB 7478, syntype, 57.8 mm SL, rio Cadeia above of the large waterfalls, Santa Maria do Herval, Rio Grande do Sul, Brazil.
Fig. 11 in Redescription of Astyanax obscurus (Hensel, 1870) and A. laticeps (Cope, 1894) (Teleostei: Characidae): two valid freshwater species originally described from rivers of Southern Brazil
Fig. 11. Tukey box plots of number of branched anal-fin rays in Astyanax laticeps populations by river drainages from south to north. Mean represented by thick vertical bar, and 25th and 75th percetiles as lateral borders of box plots.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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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.