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8 results for “erminea”
Fig. 3 in Two new species of Begonia sect. Erminea (Begoniaceae) from Nosy Mangabe in Madagascar
Fig. 3. – Begonia pteridoides Scherber. & Duruiss. (A-D) and Begonia nosymangabensis Scherber. & Duruiss. (E-F). A. Habit in cultivation; B. Stem; C. Leaf, abaxial side; D. Young plant showing juvenile leaves; E. Habit in cultivation; F. Stem. [Photos: A-D, F: David Scherberich; E: Evelyne Bouquet]
Fig. 2 in Two new species of Begonia sect. Erminea (Begoniaceae) from Nosy Mangabe in Madagascar
Fig. 2. – Begonia pteridoides Scherber. & Duruiss. A. Habit; B. Leaf, adaxial side; C. Male flower, front view; D. Male flower, side view; E. Androecium; F. Female flower, face view; G. Female flower, side view; H. Styles and stigmas; I. Ovary; J. Ovary cross-section. [Scherberich 1148, LYJB] [Drawing: Vanessa Damianthe]
Fig. 1 in Two new species of Begonia sect. Erminea (Begoniaceae) from Nosy Mangabe in Madagascar
Fig. 1. – Begonia nosymangabensis Scherber. & Duruiss. A. Habit; B. Leaf, adaxial side; C. Male flower, front view; D. Male flower, side view; E. Androecium; F. Female flower, face view; G. Female flower, side view; H. Styles and stigmas; I. Ovary; J. Ovary cross-section. [Scherberich 1132, LYJB] [Drawing: Vanessa Damianthe]
FIG. 1 in Three new species of Begonia sect. Erminea (Begoniaceae) from north-east Madagascar
FIG. 1. — Geographic distribution of Begonia ambanizanensis Scherber. & Duruiss., sp. nov., Begonia ambodiforahensis Scherber. & Duruiss., sp. nov. and Begonia harimalalae Scherber. & Duruiss., sp. nov. in north-east Madagascar.
Fig. 1 in Morphometric Criteria For Distinguishing Species And Age-Cohorts Of Ermine (Mustela Erminea) And Long-Tailed Weasel (M. Frenata)
Fig. 1. Distribution of ermine (left) and long-tailed weasel (right) species in North America (adapted from FAGERSTONE 1987). Inset shows long-tailed weasel distribution in Mexico and Central America;
Data from: Whole-genome analysis of Mustela erminea finds that pulsed hybridization impacts evolution at high-latitudes
At high-latitude, climatic shifts hypothetically drove episodes of divergence during isolation in glacial refugia, or ice-free pockets of land that enabled terrestrial species persistence. Upon glacial recession, populations can expand and often come into contact, resulting in admixture between previously isolated groups. To understand how recurrent periods of isolation and contact have impacted evolution at high latitudes, we investigated introgression in the stoat (Mustela erminea), a Holarctic mammalian carnivore, using whole-genome sequences. We identify two temporally isolated introgression events coincident with large-scale climatic shifts: contemporary introgression in a mainland contact zone and ancient contact ~ 200 km south along North America's North Pacific Coast. Repeated episodes of gene flow highlight the central role of cyclic climates in structuring high-latitude diversity, through refugial divergence and subsequent introgressive hybridization. Introgression followed by allopatry (e.g., insularization) may contribute to expedited divergence of island taxa experiencing substantial glacial flux.
Data from: Whole-genome analysis of Mustela erminea finds that pulsed hybridization impacts evolution at high-latitudes
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Subspecies and Distribution. M. e. erminea Linnaeus, 1758 — Finland, Norway, NW Russia, and Sweden. M. e. aestiva Kerr, 1792 — most of mainland N & C Europe to C Asia in Kazakhstan, Kyrgyzstan, and Tajikistan. M. e. alascensis Merriam, 1896 — S Alaska. M. e. anguinae Hall, 1932 — SW Canada (Vancouver I, British Columbia). M. e. arctica Merriam, 1896 — Alaska and NW Canada. M. e. bangsi Hall, 1945 — C Canada and NC USA. M. e. celenda Hall, 1944 — Alaska (Prince of Wales I). M.e. cicognanii Bonaparte, 1838 — SE Canada and NE USA. M. e. fallenda Hall, 1945 — W Canada (British Columbia) and NW USA (N Washington). M. e. ferghanae Thomas, 1895 — Afghanistan, N India, and Pakistan. M.e. gulosa Hall, 1945 — NW USA (E Washington). M.e. haidarum Preble, 1898 — W Canada (Queen Charlotte Is, British Columbia). M.e. hibernica Thomas & Barrett-Hamilton, 1895 — Ireland. M.e. imatis Hall, 1944 — Alaska (Baranof I). M.e. invicta Hall, 1945 — SW Canada (Alberta) and NW USA (Idaho & Montana). M.e. kadiacensis Merriam, 1896 — Alaska (Kodiak I). M.e. kaneti Baird, 1857 — NE China, Russia (E Siberia). M.e. karaginensis Jurgenson, 1936 — NE Russia (Karaginsky I). M.e. lymani Hollister, 1912 — E Russia (Altai Mts, Siberia). M.e. minima Cavazza, 1912 — Switzerland. M.e. mongolica Ognev, 1928 — NW China and Mongolian Altai. M. e. muricus Bangs, 1899 — USA (N California, Colorado, Idaho, New Mexico, Nevada, Oregon, South Dakota, Utah & Wyoming). M. e. nippon Cabrera, 1913 — Japan. M.e. olympica Hall, 1945 — NW USA (Olympic Peninsula, Washington). M.e. polaris Barrett-Hamilton, 1904 — Greenland. M.e.richardsonii Bonaparte, 1838 — N Canada. M.e. ricinae G. S. Miller, 1907 — Scotland (Islay I). M.e.salva Hall, 1944 — SE Alaska (Admiralty I). M.e.seclusa Hall, 1944 — SE Alaska (Suemez I). M.e.sempler Sutton & Hamilton, 1932 — Canada (Franklin & Keewatin Districts). M.e.stabilis Barrett-Hamilton, 1904 — Great Britain. M.e.streatori Merriam, 1896 — W USA (NE California, Oregon & coastal Washington). M.e.teberdina Kornejv, 1941 — Russian Caucasus. M.e. tobolica Ognev, 1923 — W Siberia. Introduced to New Zealand. in Mustelidae
Subspecies and Distribution. M. e. erminea Linnaeus, 1758 — Finland, Norway, NW Russia, and Sweden. M. e. aestiva Kerr, 1792 — most of mainland N & C Europe to C Asia in Kazakhstan, Kyrgyzstan, and Tajikistan. M. e. alascensis Merriam, 1896 — S Alaska. M. e. anguinae Hall, 1932 — SW Canada (Vancouver I, British Columbia). M. e. arctica Merriam, 1896 — Alaska and NW Canada. M. e. bangsi Hall, 1945 — C Canada and NC USA. M. e. celenda Hall, 1944 — Alaska (Prince of Wales I). M.e. cicognanii Bonaparte, 1838 — SE Canada and NE USA. M. e. fallenda Hall, 1945 — W Canada (British Columbia) and NW USA (N Washington). M. e. ferghanae Thomas, 1895 — Afghanistan, N India, and Pakistan. M.e. gulosa Hall, 1945 — NW USA (E Washington). M.e. haidarum Preble, 1898 — W Canada (Queen Charlotte Is, British Columbia). M.e. hibernica Thomas & Barrett-Hamilton, 1895 — Ireland. M.e. imatis Hall, 1944 — Alaska (Baranof I). M.e. invicta Hall, 1945 — SW Canada (Alberta) and NW USA (Idaho & Montana). M.e. kadiacensis Merriam, 1896 — Alaska (Kodiak I). M.e. kaneti Baird, 1857 — NE China, Russia (E Siberia). M.e. karaginensis Jurgenson, 1936 — NE Russia (Karaginsky I). M.e. lymani Hollister, 1912 — E Russia (Altai Mts, Siberia). M.e. minima Cavazza, 1912 — Switzerland. M.e. mongolica Ognev, 1928 — NW China and Mongolian Altai. M. e. muricus Bangs, 1899 — USA (N California, Colorado, Idaho, New Mexico, Nevada, Oregon, South Dakota, Utah & Wyoming). M. e. nippon Cabrera, 1913 — Japan. M.e. olympica Hall, 1945 — NW USA (Olympic Peninsula, Washington). M.e. polaris Barrett-Hamilton, 1904 — Greenland. M.e.richardsonii Bonaparte, 1838 — N Canada. M.e. ricinae G. S. Miller, 1907 — Scotland (Islay I). M.e.salva Hall, 1944 — SE Alaska (Admiralty I). M.e.seclusa Hall, 1944 — SE Alaska (Suemez I). M.e.sempler Sutton & Hamilton, 1932 — Canada (Franklin & Keewatin Districts). M.e.stabilis Barrett-Hamilton, 1904 — Great Britain. M.e.streatori Merriam, 1896 — W USA (NE California, Oregon & coastal Washington). M.e.teberdina Kornejv, 1941 — Russian Caucasus. M.e. tobolica Ognev, 1923 — W Siberia. Introduced to New Zealand.
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