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173 results for “South Carolina”
Subspecies and Distribution. C.r.rafinesquiiLesson,1827—E&SIllinois,W&SIndiana,SOhio,SEMissouri,Ken-tucky,Tennessee,WNorthCarolina,andEArkansas(EUSA). C. r. macrotis Le Conte, 1831 — E North Carolina, South Carolina, Georgia, Florida, Alabama, Mississippi, Louisiana, E Texas, and extreme SW Arkansas. in Vespertilionidae
Subspecies and Distribution. C.r.rafinesquiiLesson,1827—E&SIllinois,W&SIndiana,SOhio,SEMissouri,Ken-tucky,Tennessee,WNorthCarolina,andEArkansas(EUSA). C. r. macrotis Le Conte, 1831 — E North Carolina, South Carolina, Georgia, Florida, Alabama, Mississippi, Louisiana, E Texas, and extreme SW Arkansas.
Subspecies and Distribution. P.m.maniculatusWagner,1845—SManitoba,Ontario,Quebec,andLabrador,Canada. P.m.abietorumBangs,1896—NewBrunswickandNovaScotia,Canada,andMaine, USA. P.m.alpinusCowan,1937—restrictedtoasmallregioninSEBritishColumbia,Canada . P.m.anacapaevonBloeker,1942—knownonlyfromWestAnacapaIandsurroundingIs,California,USA. P.m.angustusHall,1932—knownonlyfromSWpartofVancouverI,BritishColumbia, Canada. P.m.anticostiensisMoulthrop,1937—knownonlyfromthetypelocalityonEAnticostiI,Quebec,Canada. P.m.argentatusCopeland&Church,1906—knownonlyfromthetypelocalityonGrandMananI,NewBrunswick,Canada. P.m.artemisiaeRhoads,1894—fromSCBritishColumbia,Canada,SWtoWWyoming, USA. P.m.assimilisNelson&Goldman,1931—knownonlyfromthetypelocalityonCoronadoIs,BajaCalifornia,Mexico. P.m.austerusBaird,1855—WCWashington,USA. P.m.bairdiiHoy&Kennicott,1857—mostoftheECportionoftheUSA. P.m.balaclavaeMcCabe&Cowan,1945—knownonlyfromthetypelocalityonBalaklavaI,BritishColumbia,Canada. P.m.blandusOsgood,1904—SCUSAStoSanLuisPotosi,Guanajauto,andJalisco, Mexico. P.m.borealisMearns,1911—NWCanada. P.m.catalinaeElliot,1903—knownonlyfromSantaCatalinaI,California,USA. P.m.cmenitius|.A.Allen,1898—knownonlyfromthetypelocalityonSanRoqueI, BajaCalifornia,Mexico. P.m.clementisMearns,1896—knownonlyfromSanClementeI,California,USA. P.m.coolidge:Thomas,1898—SBajaCaliforniaandBajaCaliforniaSur,Mexico. P.m.dorsalisNelson&Goldman,1931—knownonlyfromthetypelocalityonNatividadI,BajaCalifornia,Mexico. P.m.dubiusJ.A.Allen,1898—knownonlyfromthetypelocalityonTodosSantosI, BajaCalifornia,Mexico. P.m.elususNelson&Goldman,1931—knownonlyfromSantaBarabaraandSutilIs, California,USA. P.m.eremusOsgood,1909—knownonlyfromGrindstoneI,Quebec,Canada. P.m.exiguusJ.A.Allen,1898—knownonlyfromSanMartinI,BajaCalifornia,Mexico. P.m.exterusNelson&Goldman,1931—knownonlyfromthetypelocalityonSanNicolasI,California,USA. P.m.fulvusOsgood,1904—fromCPueblaandVeracruzStoCOaxaca,Mexico. P.m.gambeliiBaird,1858—N&WCalifornia,USA,SintoNBajaCalifornia,Mexico. P.m.georgiensisHall,1938—knownonlyfromthetypelocalityonTexadaIandsurroundingIs,BritishColumbia,Canada. P.m.geronimensisJ.A.Allen,1898—knownonlyfromthetypelocalityonSanGeronimoI,BajaCalifornia,Mexico. P.m.gracilisLeConte,1855—OntarioandSQuebec,Canada,S&EtoWisconsin, Michigan,andNEUSA.FP.m.hollister:Osgood,1909—knownonlyfromSanJuanIandsurroundingIs,Washington,USA. P.m.huey:Nelson&Goldman,1932—knownonlyfromthetypelocalityonasmallunnamedIinGonzagaBay,BajaCalifornia,Mexico. P. m. inclarus Goldman, 1939 — known only from Fremont I in Great Salt Lake, Utah, USA. P.m. labecula Elliot, 1903 — from Durango S to Michoacan and Morelos, Mexico. P. m. luteus Osgood, 1905 — from South Dakota S to W Texas, USA. P. m. magdalenae Osgood, 1909 — Magdalena I and surrounding mainland areas, Baja California, Mexico. P.m. margaritae Osgood, 1909 — known only from Margarita I, Baja California, Mexico. Pm. nebrascensis Coues, 1877 — from S Alberta and Saskatchewan, Canada, S to NW Texas, USA. Pm. nubiterrae Rhoads, 1896 — from W New York S to North Carolina, USA. Pm. ozarkiarum Black, 1935 — from NE Oklahoma and SW Missouri S to W Arkansas and NC edge of Texas, USA. P. m. pallescensJ. A. Allen, 1896 — NC to SC Texas, USA. Pm. plumbeus C. F. Jackson, 1939 — E Quebec, Canada. Pm. rubidus Osgood, 1901 — from SW Washington S along the Pacific Coast to C California, USA. P. m. rufinus Merriam, 1890 — from N California S to SC Arizona and New Mexico, USA. P. m. sanctaerosae von Bloeker, 1940 — known only from Santa Rosa I, California, USA. P.m. santacruzae Nelson & Goldman, 1931 — known only from Santa Cruz I, California, USA. Pm. saturatus Bangs, 1897 — known only from Saturna I, British Columbia, Canada. Pm. saxamans McCabe & Cowan, 1945 — known only from Duncan I and surrounding Is, British Columbia, Canada. Pm. serratus Davis, 1939 — restricted to a small region in C Idaho, USA. Pm. sonoriensis Le Conte, 1853 — from SE Oregon and S Idaho, USA, S to N edge of Sonora, Mexico. Pm. streatori Nelson & Goldman, 1931 — known only from San Miguel I and surrounding Is, California, USA. in Cricetidae
Subspecies and Distribution. P.m.maniculatusWagner,1845—SManitoba,Ontario,Quebec,andLabrador,Canada. P.m.abietorumBangs,1896—NewBrunswickandNovaScotia,Canada,andMaine, USA. P.m.alpinusCowan,1937—restrictedtoasmallregioninSEBritishColumbia,Canada . P.m.anacapaevonBloeker,1942—knownonlyfromWestAnacapaIandsurroundingIs,California,USA. P.m.angustusHall,1932—knownonlyfromSWpartofVancouverI,BritishColumbia, Canada. P.m.anticostiensisMoulthrop,1937—knownonlyfromthetypelocalityonEAnticostiI,Quebec,Canada. P.m.argentatusCopeland&Church,1906—knownonlyfromthetypelocalityonGrandMananI,NewBrunswick,Canada. P.m.artemisiaeRhoads,1894—fromSCBritishColumbia,Canada,SWtoWWyoming, USA. P.m.assimilisNelson&Goldman,1931—knownonlyfromthetypelocalityonCoronadoIs,BajaCalifornia,Mexico. P.m.austerusBaird,1855—WCWashington,USA. P.m.bairdiiHoy&Kennicott,1857—mostoftheECportionoftheUSA. P.m.balaclavaeMcCabe&Cowan,1945—knownonlyfromthetypelocalityonBalaklavaI,BritishColumbia,Canada. P.m.blandusOsgood,1904—SCUSAStoSanLuisPotosi,Guanajauto,andJalisco, Mexico. P.m.borealisMearns,1911—NWCanada. P.m.catalinaeElliot,1903—knownonlyfromSantaCatalinaI,California,USA. P.m.cmenitius|.A.Allen,1898—knownonlyfromthetypelocalityonSanRoqueI, BajaCalifornia,Mexico. P.m.clementisMearns,1896—knownonlyfromSanClementeI,California,USA. P.m.coolidge:Thomas,1898—SBajaCaliforniaandBajaCaliforniaSur,Mexico. P.m.dorsalisNelson&Goldman,1931—knownonlyfromthetypelocalityonNatividadI,BajaCalifornia,Mexico. P.m.dubiusJ.A.Allen,1898—knownonlyfromthetypelocalityonTodosSantosI, BajaCalifornia,Mexico. P.m.elususNelson&Goldman,1931—knownonlyfromSantaBarabaraandSutilIs, California,USA. P.m.eremusOsgood,1909—knownonlyfromGrindstoneI,Quebec,Canada. P.m.exiguusJ.A.Allen,1898—knownonlyfromSanMartinI,BajaCalifornia,Mexico. P.m.exterusNelson&Goldman,1931—knownonlyfromthetypelocalityonSanNicolasI,California,USA. P.m.fulvusOsgood,1904—fromCPueblaandVeracruzStoCOaxaca,Mexico. P.m.gambeliiBaird,1858—N&WCalifornia,USA,SintoNBajaCalifornia,Mexico. P.m.georgiensisHall,1938—knownonlyfromthetypelocalityonTexadaIandsurroundingIs,BritishColumbia,Canada. P.m.geronimensisJ.A.Allen,1898—knownonlyfromthetypelocalityonSanGeronimoI,BajaCalifornia,Mexico. P.m.gracilisLeConte,1855—OntarioandSQuebec,Canada,S&EtoWisconsin, Michigan,andNEUSA.FP.m.hollister:Osgood,1909—knownonlyfromSanJuanIandsurroundingIs,Washington,USA. P.m.huey:Nelson&Goldman,1932—knownonlyfromthetypelocalityonasmallunnamedIinGonzagaBay,BajaCalifornia,Mexico. P. m. inclarus Goldman, 1939 — known only from Fremont I in Great Salt Lake, Utah, USA. P.m. labecula Elliot, 1903 — from Durango S to Michoacan and Morelos, Mexico. P. m. luteus Osgood, 1905 — from South Dakota S to W Texas, USA. P. m. magdalenae Osgood, 1909 — Magdalena I and surrounding mainland areas, Baja California, Mexico. P.m. margaritae Osgood, 1909 — known only from Margarita I, Baja California, Mexico. Pm. nebrascensis Coues, 1877 — from S Alberta and Saskatchewan, Canada, S to NW Texas, USA. Pm. nubiterrae Rhoads, 1896 — from W New York S to North Carolina, USA. Pm. ozarkiarum Black, 1935 — from NE Oklahoma and SW Missouri S to W Arkansas and NC edge of Texas, USA. P. m. pallescensJ. A. Allen, 1896 — NC to SC Texas, USA. Pm. plumbeus C. F. Jackson, 1939 — E Quebec, Canada. Pm. rubidus Osgood, 1901 — from SW Washington S along the Pacific Coast to C California, USA. P. m. rufinus Merriam, 1890 — from N California S to SC Arizona and New Mexico, USA. P. m. sanctaerosae von Bloeker, 1940 — known only from Santa Rosa I, California, USA. P.m. santacruzae Nelson & Goldman, 1931 — known only from Santa Cruz I, California, USA. Pm. saturatus Bangs, 1897 — known only from Saturna I, British Columbia, Canada. Pm. saxamans McCabe & Cowan, 1945 — known only from Duncan I and surrounding Is, British Columbia, Canada. Pm. serratus Davis, 1939 — restricted to a small region in C Idaho, USA. Pm. sonoriensis Le Conte, 1853 — from SE Oregon and S Idaho, USA, S to N edge of Sonora, Mexico. Pm. streatori Nelson & Goldman, 1931 — known only from San Miguel I and surrounding Is, California, USA.
Distribution. SE Canada (S Ontario and S Quebec) and NE USA (W Maine, New Hampshire, Vermont, New York, Massachusetts, N Connecticut, N Rhode Island, Ohio, Pennsylvania, N New Jersey, West Virginia, NW Maryland, W Virginia, E Kentucky, E Tennessee, W North Carolina, extreme NE Georgia, and extreme NW South Carolina). in Talpidae
Distribution. SE Canada (S Ontario and S Quebec) and NE USA (W Maine, New Hampshire, Vermont, New York, Massachusetts, N Connecticut, N Rhode Island, Ohio, Pennsylvania, N New Jersey, West Virginia, NW Maryland, W Virginia, E Kentucky, E Tennessee, W North Carolina, extreme NE Georgia, and extreme NW South Carolina).
Subspecies and Distribution. C.c.cristataLinnaeus,1758—SECanada(SManitoba,C&SOntario,SQuebec,andNewfoundland)andNEUSA(N&CMinnesota,Wisconsin,Michigan,NewYork,Vermont,NewHampshire,Maine,Massachusetts,Connecticut,RhodeIsland,NOhio,Pennsylvania,NewJersey,EWestVirginia,NVirginia,Maryland,andDelaware). C.c. nigra R. W. Smith, 1940 — E USA (S West Virginia, S Virginia, W & E North Carolina, E Tennessee, E South Carolina, and SE Georgia). in Talpidae
Subspecies and Distribution. C.c.cristataLinnaeus,1758—SECanada(SManitoba,C&SOntario,SQuebec,andNewfoundland)andNEUSA(N&CMinnesota,Wisconsin,Michigan,NewYork,Vermont,NewHampshire,Maine,Massachusetts,Connecticut,RhodeIsland,NOhio,Pennsylvania,NewJersey,EWestVirginia,NVirginia,Maryland,andDelaware). C.c. nigra R. W. Smith, 1940 — E USA (S West Virginia, S Virginia, W & E North Carolina, E Tennessee, E South Carolina, and SE Georgia).
Fig. 1 in Checklist of the Rove Beetles (Coleoptera: Staphylinidae) of South Carolina, Based on Published Records
Fig. 1. States and regions with lists of species of Staphylinidae. Red = state list; blue = regional list; green = unpublished list. See text for details.
A Spatiotemporal Dataset of Irrigated Agricultural Areas Across the Coastal Plain Region of South Carolina; USA
<p>A Spatiotemporal Dataset of Irrigated Agricultural Areas Across the Coastal Plain Region of South Carolina; USA</p>
Diversity, seasonal abundance, and environmental drivers of chaetognath populations in North Inlet Estuary, South Carolina, USA
<p>Chaetognaths (Phylum: Chaetognatha) are one of the most abundant phyla of zooplankton worldwide and play an important role in marine trophic interactions. Although the role of chaetognaths in global ecosystems is well understood, the spatial variation and environmental drivers of estuarine chaetognath populations is poorly understood. To provide the first known record of chaetognath species composition in a coastal estuary in the south-eastern USA, chaetognaths were identified and quantified from zooplankton samples collected on a monthly basis in 2019 and 2020 from North Inlet Estuary in South Carolina. <em>Parasagitta tenuis </em>was the most abundant species of the five found, making up 33% of total abundance. The egg presence of these chaetognaths was further analyzed to gauge reproductive cycles. Abundance and egg presence were compared with surface and bottom measurements of temperature, salinity, and dissolved oxygen levels to determine the driving abiotic factors behind chaetognath's seasonal variability and reproductive cycles. Temperature, salinity, and dissolved oxygen all had low (r < ± 0.29), non-significant correlations with abundance. Chaetognath egg production was most significantly associated with dissolved oxygen (p < 0.001) and seasonal changes in temperature (p < 0.001). Our initial findings indicate the continued abundance of chaetognath in a local estuary is dependent on abiotic factors that are strongly influenced by a changing climate. </p>
Diversity, seasonal abundance, and environmental drivers of chaetognath populations in North Inlet Estuary, South Carolina, USA
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Data from: Zooplankton species diversity in the temporary wetland system of the Savannah River Site, South Carolina, USA
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Data from: A new specimen of Agorophius pygmaeus (Agorophiidae, Odontoceti, Cetacea) from the Early Oligocene Ashley Formation of South Carolina, USA
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South Carolina Synthetic Ecosystem
South Carolina synthetic population dataset consisting of tables for persons, households, schools, and workplaces. This dataset was created by the SPEW program from 2010 ACS SF 5-Year counts; 2010 US TIGER Roads; ACS PUMS 1-Year micro data; 2013 and 2011 NCES schools; and 2009 ESRI workplaces.
Fig. 4 in Multispecies leatherback turtle assemblage from the Oligocene Chandler Bridge and Ashley formations of South Carolina, USA
Fig. 4. Ossicle of leatherback turtle cf. Egyptemys sp. (CCNHM 4289) from Oligocene of South Carolina, USA, in dorsal (A1), visceral (A2), and sutural A3) views.
Fig. 2 in Multispecies leatherback turtle assemblage from the Oligocene Chandler Bridge and Ashley formations of South Carolina, USA
Fig. 2. Ossicles of leatherback turtle Natemys sp. 1 from Oligocene of South Carolina, USA. CCNHM 5542 (A), CCNHM 5540 (B), CCNHM 4405.1– 4405.5 (C–G, respectively), CCNHM 4288 (H), and CCNHM 5541 (I), in dorsal (A1–I1), visceral (A2–I2), and sutural (A3–I3) views.
Fig. 1 in Multispecies leatherback turtle assemblage from the Oligocene Chandler Bridge and Ashley formations of South Carolina, USA
Fig. 1. The Ashley and Chandler Bridge formations and geologic context of CCNHM ossicles. A. Map of the southeastern United States. B. Map of Ashley and Chandler Bridge formation exposures on the coast of South Carolina. Stars denote Oligocene dermochelyid localities. C. Stratigraphic column of the Ashley and Chandler Bridge formations.
An integrated population model of a high-density coyote population in South Carolina
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Fig. 3 in Acaricide efficacy and resistance in South Carolina tomato populations of twospotted spider mite
Fig. 3. Median plot damage ratings in a 2016 acaricide efficacy trial conducted in South Carolina, USA. The dashed line indicates the overall median across treatments. Plots were rated on a 1 to 10 scale, with "1" indicating no damage and "10" indicating complete leaf necrosis.
Figure 40-48 in Weevils of the genus Cercopeus Schoenherr from South Carolina, USA (Coleoptera: Curculionidae: Entiminae)
Figure 40-48. Female genitalia of Cercopeus species: a. tergum VII, dorsal view; b. tergum VIII, dorsal view; c. sternum VIII, ventral view; d. coxite, lateral view; e. spermatheca. 40) C. alexi. 41) C. chrysorrhoeus. 42) C. cornelli. 43) C. femoratus. 44) C. maspavancus. 45) C. paulus. 46) C. skelleyi. 47) C. strigicollis. 48) C. tibialis. Scale bars: 0.5 mm for a, b and c; 0.2 mm for d and e.
Daily Water Sample Nutrient Data for North Inlet Estuary, South Carolina, from 1978 to 1992, North Inlet LTER
This data package consists of Daily Water Sample Nutrient Data for North Inlet Estuary, South Carolina, from 1978 to 1992, North Inlet LTER. Its purpose is to establish a long term data base on the nutrient dynamics of a salt marsh estuarine system. This data can be used in correlation with a number of other estuarine data sets to obtain a broader definition of the over all estuarine ecosystem.
LTER Oyster Landing Biweekly Fish Sampling in Oyster Landing Creek, North Inlet Estuary, Georgetown, South Carolina, from 1981 to 1992, North Inlet LTER
This data package consists of Biweekly Fish Sampling data in Oyster Landing Creek, North Inlet Estuary, Georgetown, South Carolina, from 1981 to 1992, North Inlet LTER. The purpose for the long term study of the population dynamics of fish, shrimp, and crab in the North Inlet estuary are: 1) to discover the abundance, distribution and life history patterns of these organisms which occur in this area; 2) to maintain long-term population information so it can be used to compare with future short-term fish population studies proposed by investigators from USC and other universities, as well as investigators at the Baruch Laboratory; and 3) to relate this population information to the population dynamics of zooplankton, epibenthos, benthic macrofaua, and meiofauna.
Zooplankton Data for North Inlet Estuary, South Carolina, from 1981 to 1992, North Inlet LTER
This data package consists of Zooplankton Data for North Inlet Estuary, South Carolina, from 1981 to 1992, North Inlet LTER. The purpose of the long term monitoring of zooplankton was to characterize the fauna in the water column larger than or equal to 153 microns and to obtain some basic information on each of the taxa encountered there. A sampling regime of collections made at regular biweekly intervals was implemented to provide the best quantitative assessment of long term changes in the zooplankton population dynamics.
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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)
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DANDI Archive for NWB datasets
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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.