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.
148
datasets available to search
ShareScore release 0.9.0
Dataset results
148 results for “coastal basin”
FIGURE 13 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 13. Land filling for civil construction projects in the type-locality of Hypsolebias gongobira and H. longignatus.
FIGURE 9 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 9. Bayesian inference based on the mitochondrial gene cox1 used for lineage delimitation of the Hypsolebias antenori species-group. Vertical bars represent the number of lineages delimited by ABGD (7), sGMYC (6), mGMYC (11), and b-PTP (10). Numbers adjacent to nodes represent posterior probabilities; values <0.50% are not shown.
FIGURE 12 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 12. Environmental impact of the duplication of the CE-40 highway in the type-locality of Hypsolebias gongobira and H. longignatus.
FIGURE 11. Hypsolebias longignatus, UFRN 5846, male 35.8 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 11. Hypsolebias longignatus, UFRN 5846, male 35.8 mm SL: Brazil, Ceará, Aquiraz, rio Pacoti basin.
FIGURE 5. Hypsolebias bonita new species, MZUSP 129608 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 5. Hypsolebias bonita new species, MZUSP 129608, male, paratype, 38.6 mm SL: Brazil, Rio Grande do Norte, Baraúna, Furna Feia National Park.
FIGURE 4 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 4. Type-locality of Hypsolebias gongobira new species, Brazil, Ceará, Aquiraz, rio Pacoti basin.
FIGURE 15 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 15. Locality of H. antenori, Brazil, Ceará, Russas, seasonal pool in the floodplain of the rio Jaguaribe basin.
FIGURE 3. Hypsolebias gongobira new species, MZUSP 129607 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 3. Hypsolebias gongobira new species, MZUSP 129607, female, paratype, 35 mm SL: Brazil, Ceará, Aquiraz, rio Pacoti basin.
FIGURE 1 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 1. Map of northeastern Brazil showing the distribution of the Hypsolebias antenori species-group. Stars represent type localities, and circles indicate sampled localities. Hypsolebias bonita new species in pink, H. antenori in red, H. gongobira new species in orange (syntopic with H. longignatus), H. martinsi in yellow, H. coamazonicus in green, H. faouri in light blue, H. igneus in dark blue, and H. nudiorbitatus in purple. Dark blue lines represent hydrographic basins of the Caatinga ecoregions, Maranhão-Piauí (MAPE), Mid-Northeastern Caatinga (MNCE), Northeastern Atlantic Forest (NAFE) São Francisco (SFRE).
FIGURE 8 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 8. Caudal fin of living males: Hypsolebias gongobira new species (A), H. antenori (B) e H. bonita new species (C).
FIGURE 7 in Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil
FIGURE 7. Type-locality of Hypsolebias bonita new species, Brazil, Rio Grande do Norte, Baraúna, seasonal pool in the Furna Feia National Park.
Dissolved Mn(III) is a key redox intermediate in sediments of a seasonally euxinic coastal basin
<p>Dataset and computer model used in the article "Dissolved Mn(III) is a key redox intermediate in sediments of a seasonally euxinic coastal basin" in Biogeosciences.</p>
Subspecies and Distribution. P. o. onca Linnaeus, 1758 — Amazon and Orinoco basin rainforests. P.o. arizonensis Goldman, 1932 — SW USA (Arizona) to NW Mexico (Sonora). P. o. centralis Mearns, 1901 — Nicaragua to Colombia. P. o. goldmani Mearns, 1901 — Yucatan Peninsula of Mexico S to Belize and N Honduras. P. o. hernandesi Gray, 1857 — W Mexico (S Sonora to Oaxaca). P. o. palustris Ameghino, 1888 — S Brazil S through Uruguay to N Argentina (the Rio Negro in Chaco province). P. o. paraguensis Hollister, 1914 — Paraguay. P. o. peruviana de Blainville, 1843 — coastal regions of Ecuador and Peru. P.o. veraecrucis Nelson & Goldman, 1933 — S USA (C Texas, now extinct) to SE Mexico (Chiapas). in Felidae
Subspecies and Distribution. P. o. onca Linnaeus, 1758 — Amazon and Orinoco basin rainforests. P.o. arizonensis Goldman, 1932 — SW USA (Arizona) to NW Mexico (Sonora). P. o. centralis Mearns, 1901 — Nicaragua to Colombia. P. o. goldmani Mearns, 1901 — Yucatan Peninsula of Mexico S to Belize and N Honduras. P. o. hernandesi Gray, 1857 — W Mexico (S Sonora to Oaxaca). P. o. palustris Ameghino, 1888 — S Brazil S through Uruguay to N Argentina (the Rio Negro in Chaco province). P. o. paraguensis Hollister, 1914 — Paraguay. P. o. peruviana de Blainville, 1843 — coastal regions of Ecuador and Peru. P.o. veraecrucis Nelson & Goldman, 1933 — S USA (C Texas, now extinct) to SE Mexico (Chiapas).
Distribution. SE Australia, from the McPherson and Border ranges in SE Queensland, S to Victoria and SE South Australia; it is absent from the coastal drainages of the Great Dividing Range, S at least to the Wallamba River, and W of the Great Dividing Range in New South Wales (but it probably occurs to the limit of tree growth on the Southern Tableland), and from the inland draining catchments of the Murray Basin in Victoria. in Acrobatidae
Distribution. SE Australia, from the McPherson and Border ranges in SE Queensland, S to Victoria and SE South Australia; it is absent from the coastal drainages of the Great Dividing Range, S at least to the Wallamba River, and W of the Great Dividing Range in New South Wales (but it probably occurs to the limit of tree growth on the Southern Tableland), and from the inland draining catchments of the Murray Basin in Victoria.
Subspecies and Distribution. P. l. longimembris Coues, 1875 — SW USA (Mojave Desert and Transverse Ranges, SW California). P. l. aestivus Huey, 1928 — NW Mexico (W base Sierra Juarez to Valle de la Trinidad, N Baja California). P.l. arizonensis Goldman, 1931 — SW USA (SC Utah and NC Arizona to SE Nevada). P. l.bangsi Mearns, 1898 — SW USA (W Colorado Desert of S California). P. l. bombycinus Osgood, 1907 — SW USA and NW Mexico (lower Colorado River Valley of SE California, SW Arizona, NE Baja California, and NW Sonora). P. l. brevinasus Osgood, 1900 — SW USA (arid coastal basins of SW California). P. l. gulosus Hall, 1941 — W USA (along the W margin of former Pleistocene Lake Bonneville in the Great Basin of E Nevada and W Utah). P. l. internationalis Huey, 1939 — SW USA and NW Mexico (SC California and adjacent NC Baja California). P. l. kinoensis Huey, 1935 — NW Mexico (disjunct and geographically restricted population along Bahia Kino, W Sonora), but may be extinct. P. l. nevadensis Merriam, 1894 — W USA (Great Basin of SE Oregon, NE California, and NC Nevada). P. l. pacificus Mearns, 1898 — SW USA (coastal plains of SW California to the USA-Mexico border). P. I. panamintinus Merriam, 1894 — SW USA (Great Basin of W Nevada and SE California). P. l. pimensis Huey, 1937 — SW USA (disjunct distribution in SC Arizona). P. l. salinensis Bole, 1937 — SW USA (restricted distribution in the Salinas Valley of SE California). P. l. tularensis Richardson, 1937 — SW USA (restricted distribution in the upper valley of the Kern River, SC California). P. l. venustus Huey, 1930 — NW Mexico (known only from the type locality of San Agustin, NC Baja California). in Heteromyidae
Subspecies and Distribution. P. l. longimembris Coues, 1875 — SW USA (Mojave Desert and Transverse Ranges, SW California). P. l. aestivus Huey, 1928 — NW Mexico (W base Sierra Juarez to Valle de la Trinidad, N Baja California). P.l. arizonensis Goldman, 1931 — SW USA (SC Utah and NC Arizona to SE Nevada). P. l.bangsi Mearns, 1898 — SW USA (W Colorado Desert of S California). P. l. bombycinus Osgood, 1907 — SW USA and NW Mexico (lower Colorado River Valley of SE California, SW Arizona, NE Baja California, and NW Sonora). P. l. brevinasus Osgood, 1900 — SW USA (arid coastal basins of SW California). P. l. gulosus Hall, 1941 — W USA (along the W margin of former Pleistocene Lake Bonneville in the Great Basin of E Nevada and W Utah). P. l. internationalis Huey, 1939 — SW USA and NW Mexico (SC California and adjacent NC Baja California). P. l. kinoensis Huey, 1935 — NW Mexico (disjunct and geographically restricted population along Bahia Kino, W Sonora), but may be extinct. P. l. nevadensis Merriam, 1894 — W USA (Great Basin of SE Oregon, NE California, and NC Nevada). P. l. pacificus Mearns, 1898 — SW USA (coastal plains of SW California to the USA-Mexico border). P. I. panamintinus Merriam, 1894 — SW USA (Great Basin of W Nevada and SE California). P. l. pimensis Huey, 1937 — SW USA (disjunct distribution in SC Arizona). P. l. salinensis Bole, 1937 — SW USA (restricted distribution in the Salinas Valley of SE California). P. l. tularensis Richardson, 1937 — SW USA (restricted distribution in the upper valley of the Kern River, SC California). P. l. venustus Huey, 1930 — NW Mexico (known only from the type locality of San Agustin, NC Baja California).
Distribution. Coastal plain and interior basins of W Mexico, from S Nayarit, extreme S Durango, and SW Zacatecas S to extreme SW Chiapas, and E into W Hidalgo, W Puebla, and NW Oaxaca. in Cricetidae
Distribution. Coastal plain and interior basins of W Mexico, from S Nayarit, extreme S Durango, and SW Zacatecas S to extreme SW Chiapas, and E into W Hidalgo, W Puebla, and NW Oaxaca.
FIGURE 29 in New taxa of Tateidae (Caenogastropoda, Truncatelloidea) from springs associated with the Great Artesian Basin and Einasleigh Uplands, Queensland, with the description of two related taxa from eastern coastal drainages
FIGURE 29. Radula of Nundalia secreta n. gen. and n. sp. (C.200900). A. Half row of radula. B. Detail of central teeth. Scale bar 10 µm.
FIGURE 22 in New taxa of Tateidae (Caenogastropoda, Truncatelloidea) from springs associated with the Great Artesian Basin and Einasleigh Uplands, Queensland, with the description of two related taxa from eastern coastal drainages
FIGURE 22. Radula of Carnarvoncochlea cf. carnarvonensis (Ponder & Clark, 1990) (C.400126). A. Detail of central teeth. B. Detail of lateral and inner marginal teeth. C. Detail of outer marginal teeth. Scale bars 10 µm.
FIGURE 27 in New taxa of Tateidae (Caenogastropoda, Truncatelloidea) from springs associated with the Great Artesian Basin and Einasleigh Uplands, Queensland, with the description of two related taxa from eastern coastal drainages
FIGURE 27. Male and female reproductive anatomy of Conondalia buzwilsoni n. gen. and n. sp. (C.200788). A. Penis, showing penial duct and vas deferens. B. Prostate, with associated vas deferens and vas efferens. C. Female system from left side. D. Bursa copulatrix and seminal receptacle. Abbreviations: ag—albumen gland; avd—anterior vas deferens; bc—bursa copulatrix; cg—capsule gland; o—opening of oviduct; pd—penial duct; pvd—posterior vas deferens; pw—posterior wall of mantle cavity; ro—renal oviduct; sr—seminal receptacle; vc—ventral channel. Scale bar 200 µm.
FIGURE 21 in New taxa of Tateidae (Caenogastropoda, Truncatelloidea) from springs associated with the Great Artesian Basin and Einasleigh Uplands, Queensland, with the description of two related taxa from eastern coastal drainages
FIGURE 21. Shell and operculum of Carnarvoncochlea cf. carnarvonensis (Ponder & Clark, 1990). A. Shell (C.479955). B. Protoconch. C–E. Operculum, outer (C), and inner (D, E) sides (C.400126).
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.