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Subspecies and Distribution. M. n. nivalis Linnaeus, 1766 — China, North and South Korea, Mongolia, Russia, Taiwan, and Scandinavia. M. n. allegheniensis Rhoads, 1900 — NE USA (Allegheny Mts W to Wisconsin). M. n. boccamela Bechstein, 1800 — Corsica, Italy, Portugal, Sardinia, Sicily, and Spain. M. n. campestris Jackson, 1913 — C Great Plains, USA. M. n. eskimo Stone, 1900 — Alaska and NW Canada (Yukon). M. n. namiyer Kuroda, 1921 — Japan and the Kurile Is. M. n. numidica Pucheran, 1855 — N Africa. M. n. rnixosa Bangs, 1896 — Canada and N Great Plains of USA. M. n. vulgaris Erxleben, 1777 = W & C Europe and most of C Eurasia. Introduced to New Zealand, Malta, Crete, the Azores Is, and apparently also Sao Tome I. in Mustelidae
Subspecies and Distribution. M. n. nivalis Linnaeus, 1766 — China, North and South Korea, Mongolia, Russia, Taiwan, and Scandinavia. M. n. allegheniensis Rhoads, 1900 — NE USA (Allegheny Mts W to Wisconsin). M. n. boccamela Bechstein, 1800 — Corsica, Italy, Portugal, Sardinia, Sicily, and Spain. M. n. campestris Jackson, 1913 — C Great Plains, USA. M. n. eskimo Stone, 1900 — Alaska and NW Canada (Yukon). M. n. namiyer Kuroda, 1921 — Japan and the Kurile Is. M. n. numidica Pucheran, 1855 — N Africa. M. n. rnixosa Bangs, 1896 — Canada and N Great Plains of USA. M. n. vulgaris Erxleben, 1777 = W & C Europe and most of C Eurasia. Introduced to New Zealand, Malta, Crete, the Azores Is, and apparently also Sao Tome I.
Subspecies and Distribution. N. v. vison Schreber, 1776 — E Canada and NE USA (Allegheny Mts). N. v. aestuarina Grinnell, 1916 — SW USA (California & W Nevada). N. v. aniakensis Burns, 1964 — W Alaska. N. v. energumenos Bangs, 1896 — W Canada and NW USA. N. v. evagor Hall, 1932 — SW Canada (Vancouver I). N. v. evergladensis Hamilton, 1948 — SE USA (SW Florida). N. v. ingens Osgood, 1900 — most of Alaska and NW Canada (N Mackenzie & Yukon). N. v. lacustris Preble, 1902 — C Canada (Keewatin Region, Manitoba & Ontario). N. v. letifera Hollister, 1913 — Great Plains of USA. N. v. low Anderson, 1945 — E Canada (Labrador & Quebec). N. v. lutensis Bangs, 1898 — USA (S Carolina to Florida). N. v. melampeplus Elliot, 1903 — Alaska (Kenai Peninsula). N. v. mink Peale & Palisot de Beauvois, 1796 — SE USA. N. v. nesolestes Heller, 1909 — SW Alaska. N. v. vulgivaga Bangs, 1895 — USA (Arkansas & Louisiana). Introduced to Belarus, Belgium, China, Czech Republic, Denmark, Estonia, Finland, France, Germany, Great Britian, Iceland, Ireland, Italy, Japan (Hokkaido), Latvia, Lithuania, Netherlands, Norway, Poland, Portugal, Russia, Spain, and Sweden. in Mustelidae
Subspecies and Distribution. N. v. vison Schreber, 1776 — E Canada and NE USA (Allegheny Mts). N. v. aestuarina Grinnell, 1916 — SW USA (California & W Nevada). N. v. aniakensis Burns, 1964 — W Alaska. N. v. energumenos Bangs, 1896 — W Canada and NW USA. N. v. evagor Hall, 1932 — SW Canada (Vancouver I). N. v. evergladensis Hamilton, 1948 — SE USA (SW Florida). N. v. ingens Osgood, 1900 — most of Alaska and NW Canada (N Mackenzie & Yukon). N. v. lacustris Preble, 1902 — C Canada (Keewatin Region, Manitoba & Ontario). N. v. letifera Hollister, 1913 — Great Plains of USA. N. v. low Anderson, 1945 — E Canada (Labrador & Quebec). N. v. lutensis Bangs, 1898 — USA (S Carolina to Florida). N. v. melampeplus Elliot, 1903 — Alaska (Kenai Peninsula). N. v. mink Peale & Palisot de Beauvois, 1796 — SE USA. N. v. nesolestes Heller, 1909 — SW Alaska. N. v. vulgivaga Bangs, 1895 — USA (Arkansas & Louisiana). Introduced to Belarus, Belgium, China, Czech Republic, Denmark, Estonia, Finland, France, Germany, Great Britian, Iceland, Ireland, Italy, Japan (Hokkaido), Latvia, Lithuania, Netherlands, Norway, Poland, Portugal, Russia, Spain, and Sweden.
Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V. v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas). in Canidae
Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V. v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas).
Distribution. Great Plains in S Canada (Alberta & Saskatchewan) and USA (Montana, and from N Wyoming and SW South Dakota to C New Mexico & NW Texas). in Canidae
Distribution. Great Plains in S Canada (Alberta & Saskatchewan) and USA (Montana, and from N Wyoming and SW South Dakota to C New Mexico & NW Texas).
Subspecies and Distribution. C. l. latrans Say, 1823 — S Canada and USA (Great Plains region). C. l. cagottis Hamilton-Smith, 1839 — SE Mexico. C. l. clepticus Elliot, 1903 — Mexico (N Baja California) and USA (S California). C. l. dickeyi Nelson, 1932 — Costa Rica, El Salvador, W Honduras, Nicaragua, and Panama. C. l. frustror Woodhouse, 1850 — USA (Missouri, Kansas, parts of Oklahoma & E Texas). C. l. goldmani Merriam, 1904 — Belize, Guatemala, and S Mexico. C. l. hondurensis Goldman, 1936 — E Honduras. C. l. impavidus J. A. Allen, 1903 - W Mexico. C. l. incolatus Hall, 1934 - Alaska and NW Canada. C. l. ¡jamesi Townsend. 1912 - Mexico (Tiburon l. Baia California). c. [l.lestes lam Merriam, 1897 1897 - sw canada Canada and w USA USA Õnzenndunzain Region & NW). v C. l. mearnsi Merriam, 1897 - NW Mexico and SW USA. C. l. mıcrodon Merriam, 1897 — NE Mexico and S USA (S Texas). C. l. ochropus Eschscholtz, 1829 - W USA (W coast). C. l. peninsulaeMerriam, 1897 — Mexico (S Baja California). C. l. texensıs Bailey, 1905 - S USA (W Texas 8c New Mexico). C. l. thamnos Jackson, 1949 - N-C Canada and E USA. C. l. umpquensıs Jackson. 1949 - USA (NW coast). C. l. vigilis Merriam. 1897 — SW Mexico. Coyotes did not originally occur on the USA E coast or Florida. They (probably thamnos) have expanded into the area with the clearing of forests and been introduced to Florida and Georgia (subspecies unknown). in Canidae
Subspecies and Distribution. C. l. latrans Say, 1823 — S Canada and USA (Great Plains region). C. l. cagottis Hamilton-Smith, 1839 — SE Mexico. C. l. clepticus Elliot, 1903 — Mexico (N Baja California) and USA (S California). C. l. dickeyi Nelson, 1932 — Costa Rica, El Salvador, W Honduras, Nicaragua, and Panama. C. l. frustror Woodhouse, 1850 — USA (Missouri, Kansas, parts of Oklahoma & E Texas). C. l. goldmani Merriam, 1904 — Belize, Guatemala, and S Mexico. C. l. hondurensis Goldman, 1936 — E Honduras. C. l. impavidus J. A. Allen, 1903 - W Mexico. C. l. incolatus Hall, 1934 - Alaska and NW Canada. C. l. ¡jamesi Townsend. 1912 - Mexico (Tiburon l. Baia California). c. [l.lestes lam Merriam, 1897 1897 - sw canada Canada and w USA USA Õnzenndunzain Region & NW). v C. l. mearnsi Merriam, 1897 - NW Mexico and SW USA. C. l. mıcrodon Merriam, 1897 — NE Mexico and S USA (S Texas). C. l. ochropus Eschscholtz, 1829 - W USA (W coast). C. l. peninsulaeMerriam, 1897 — Mexico (S Baja California). C. l. texensıs Bailey, 1905 - S USA (W Texas 8c New Mexico). C. l. thamnos Jackson, 1949 - N-C Canada and E USA. C. l. umpquensıs Jackson. 1949 - USA (NW coast). C. l. vigilis Merriam. 1897 — SW Mexico. Coyotes did not originally occur on the USA E coast or Florida. They (probably thamnos) have expanded into the area with the clearing of forests and been introduced to Florida and Georgia (subspecies unknown).
On following pages: 19. Arizona Pocket Mouse (Perognathus amplus); 20. Silky Pocket Mouse (Perognathus flavus); 21. Merriam's Pocket Mouse (Perognathus merriami); 22. Olive-backed Pocket Mouse (Perognathus fasciatus); 23. Plains Pocket Mouse (Perognathus flavescens); 24. Columbia Plateau Pocket Mouse (Perognathus parvus); 25. Great Basin Pocket Mouse (Perognathus mollipilosus); 26. White-eared Pocket Mouse (Perognathus alticola). in Heteromyidae
On following pages: 19. Arizona Pocket Mouse (Perognathus amplus); 20. Silky Pocket Mouse (Perognathus flavus); 21. Merriam's Pocket Mouse (Perognathus merriami); 22. Olive-backed Pocket Mouse (Perognathus fasciatus); 23. Plains Pocket Mouse (Perognathus flavescens); 24. Columbia Plateau Pocket Mouse (Perognathus parvus); 25. Great Basin Pocket Mouse (Perognathus mollipilosus); 26. White-eared Pocket Mouse (Perognathus alticola).
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).
Subspecies and Distribution. P. f. flavus Baird, 1855 — SW USA and NC Mexico (SE Arizona, New Mexico, N & W Texas, and from NE Sonora and Chihuahua to NC Durango). P. f. bimaculatus Merriam, 1889 — SW USA (WC Arizona). P. f. bunkeri Cockrum, 1951 — SC USA (WC Great Plains of E Colorado, W Kansas, and W Oklahoma). P. f. fuliginosus Merriam, 1890 — SW USA (vicinity of San Francisco Mts and Mogollon Plateau, NC Arizona). P. f. fuscus S. Anderson, 1972 — NW Mexico (upper valley of the Rio Papigochic and watershed of the Laguna Bustillos, WC Chihuahua). P. f. goodpaster: Hoffmeister, 1956 — SW USA (restricted distribution on the Mogollon Plateau of EC Arizona). P. f. hopiensis Goldman, 1932 — SW USA (Four Corners region of SE Utah, SW Colorado, NE Arizona, and NW New Mexico). P. f. medius Baker, 1954 — NC Mexico (SE Durango, SE Coahuila, Zacatecas, W San Luis Potosi, Aguascalientes, NE Jalisco, and Guanajuato). P. f. mexicanus Merriam, 1894 — EC Mexico (Querétaro, Hidalgo, NE Michoacan, Puebla, Distrito Federal, Tlaxcala, WC Veracruz, and Morelos). P. f. pallescens Baker, 1954 — NE Mexico (SE Chihuahua, W Coahuila, and NE Durango). P. f. parviceps Baker, 1954 — WC Mexico (S Zacatecas and N Jalisco). P. f. piperi Goldman, 1917 — NC USA (N Great Plains of E Wyoming and W Nebraska). P. f. sanluisi Hill, 1952 — SW USA (San Luis Valley of SC Colorado). P. f. sonoriensis Nelson & Goldman, 1934 — NW Mexico (disjunct distribution in coastal plains of WC Sonora). in Heteromyidae
Subspecies and Distribution. P. f. flavus Baird, 1855 — SW USA and NC Mexico (SE Arizona, New Mexico, N & W Texas, and from NE Sonora and Chihuahua to NC Durango). P. f. bimaculatus Merriam, 1889 — SW USA (WC Arizona). P. f. bunkeri Cockrum, 1951 — SC USA (WC Great Plains of E Colorado, W Kansas, and W Oklahoma). P. f. fuliginosus Merriam, 1890 — SW USA (vicinity of San Francisco Mts and Mogollon Plateau, NC Arizona). P. f. fuscus S. Anderson, 1972 — NW Mexico (upper valley of the Rio Papigochic and watershed of the Laguna Bustillos, WC Chihuahua). P. f. goodpaster: Hoffmeister, 1956 — SW USA (restricted distribution on the Mogollon Plateau of EC Arizona). P. f. hopiensis Goldman, 1932 — SW USA (Four Corners region of SE Utah, SW Colorado, NE Arizona, and NW New Mexico). P. f. medius Baker, 1954 — NC Mexico (SE Durango, SE Coahuila, Zacatecas, W San Luis Potosi, Aguascalientes, NE Jalisco, and Guanajuato). P. f. mexicanus Merriam, 1894 — EC Mexico (Querétaro, Hidalgo, NE Michoacan, Puebla, Distrito Federal, Tlaxcala, WC Veracruz, and Morelos). P. f. pallescens Baker, 1954 — NE Mexico (SE Chihuahua, W Coahuila, and NE Durango). P. f. parviceps Baker, 1954 — WC Mexico (S Zacatecas and N Jalisco). P. f. piperi Goldman, 1917 — NC USA (N Great Plains of E Wyoming and W Nebraska). P. f. sanluisi Hill, 1952 — SW USA (San Luis Valley of SC Colorado). P. f. sonoriensis Nelson & Goldman, 1934 — NW Mexico (disjunct distribution in coastal plains of WC Sonora).
Distribution. Known from scattered records in the Columbia Plateau and N Great Plains of SC British Columbia (SE Canada), N & SE Washington, Oregon, WC Idaho, Montana, NE California, N Nevada, W Wyoming, and N Utah, although these populations are probably connected and additional collecting efforts are needed. in Soricidae
Distribution. Known from scattered records in the Columbia Plateau and N Great Plains of SC British Columbia (SE Canada), N & SE Washington, Oregon, WC Idaho, Montana, NE California, N Nevada, W Wyoming, and N Utah, although these populations are probably connected and additional collecting efforts are needed.
Large-eddy simulation of an atmospheric bore and associated gravity wave effects on wind farm performance in the Southern Great Plains
<p>Animations from weather radars (observations) and simulations (modeling) of an atmospheric bore and associated gravity waves during the AWAKEN field campaign from a case study on 06 June 2023. The first animation is reflectivity from the NEXRAD WSR-88D system at the Oklahoma City radar site (KTLX) operated by the National Weather Service. The second animation is wind speed at 95, 145, and 270 m agl from the Texas Tech X-Band radars at the AWAKEN site. The third and fourth animations are for simulation results using the Weather Research and Forecasting model (WRF) with two domains. The third animation is vertical velocity at 1 km agl and potential temperature at 200 m agl on domain d01, which has a horizontal grid spacing of 300 m. The fourth animation is hub-height wind speed and perturbation pressure along with simulated power output for 3 wind turbines in each of the four rows on domain d01, which has a horizontal grid spacing of 20 m. The wind turbines are NREL 2.8 MW turbines parameterized using a generalized actuator disk. </p> <p>These animations are included as supplementary material for the manuscript "Large-eddy simulation of an atmospheric bore and associated gravity wave effects on wind farm performance in the Southern Great Plains" submitted to <em>Wind Energy Science</em>. </p>
FIG. 2 in Trends in River Discharge and Water Temperature Cue Spawning Movements of Blue Sucker, Cycleptus elongatus, in an Impounded Great Plains River
FIG. 2. Delineation of seasons (vertical lines) and average discharge and water temperature with 95% confidence bands (2006–2014 and averaged among all monitoring stations) on the Missouri River in Montana within our study area when environmental covariates were measured (1 April–24 October) for movement distance and probability modeling.
FIG. 5 in Trends in River Discharge and Water Temperature Cue Spawning Movements of Blue Sucker, Cycleptus elongatus, in an Impounded Great Plains River
FIG. 5. Log-transformed and model averaged movement rate (river kilometer per week, rkm/wk; with 95% confidence bands) and predicted probability of movement (with 95% confidence bands) with increasing water temperature (8C; 'A' and 'C,' respectively) and discharge (cubic meters per second, cms; 'B' and 'D,' respectively) for transmittered Cycleptus elongatus in the Missouri River in Montana from 2006–2014. For 'A' and 'B,' the y-axis has been back-transformed for clarity.
FIG. 1 in Trends in River Discharge and Water Temperature Cue Spawning Movements of Blue Sucker, Cycleptus elongatus, in an Impounded Great Plains River
FIG. 1. Study area on the Missouri River in Montana ranging from upstream of the confluence with the Marias River to upstream of the headwaters of Fort Peck Reservoir. Locations of remote stations are denoted with a double-crossed vertical line and labeled with general location names. Locations of select dams are represented with stars on the inset map.
Data for: Evaluation of pollination traits important for hybrid wheat development in Great Plains germplasm
<p>Hybrid wheat (<em>Triticum</em> <em>aestivum</em> L.) offers potential yield advantages over conventional inbred cultivars. For hybrid wheat to be a commercial success, the cost to produce the hybrid seed needs to be minimized. Although wheat is naturally self-pollinated, hybrid wheat seed production can be improved by increasing the amount and availability of pollen for cross-pollination. This research examined 19 pollination traits using the Hard Winter Wheat Association Mapping Panel for three years. Anther extrusion, pollen 50 date (date at which a genotype has 50% of spikes pollinating), plant height, and pollination duration (last spike pollen 50 date minus first spike pollen 50 date) were identified as the most important traits for hybrid seed production. Anther extrusion, plant height, and pollen 50 date varied widely among genotypes, while pollination duration had significant genotypic differences in one year of testing. These traits also had significant genotype x year interactions, but better and poorer performers were consistent among years. Anther extrusion was weakly, negatively correlated with plant height, and high anther extrusion semi-dwarf genotypes were identified. Pollination duration was reduced in a high temperature (>30ºC) environment, and genotypic differences in pollination duration were identified only in a milder temperature (24ºC) environment. Hierarchical clustering suggested that excellent pollinator genotypes with high anther extrusion and longer pollination duration tended to pollinate early and were of short to moderate stature. Pollination traits were higher when temperatures were mild, which benefited early genotypes because they pollinated before higher temperatures limited their pollination duration.</p>
The Great Plains Internet Wellness Study for Aging
ClinicalTrials.gov study NCT04461184. IPD Sharing: NO. Countries: 1. Publications: 55.
Data from: Testing rangeland health theory in the Northern Great Plains
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Data from: Intraspecific variation of a dominant grass and local adaptation in reciprocal garden communities along a US Great Plains’ precipitation gradient: implications for grassland restoration with climate change
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Precipitation and invasive winter annual grass data for the Great Plains
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Data from: Buteo nesting ecology: evaluating nesting of Swainson's hawks in the northern Great Plains
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Data for: Evaluation of pollination traits important for hybrid wheat development in Great Plains germplasm
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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.