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301 results for “Middle Asia”
Distribution. Wide distribution in the Palearctic: from Europe to Russian Far East, North and South Korea, and Japan; also N Africa, Middle East, C Asia, Sub-Himalayan zone, S India, Sri Lanka, C, E & S China, Taiwan, Indochina, and Sumatra. in Mustelidae
Distribution. Wide distribution in the Palearctic: from Europe to Russian Far East, North and South Korea, and Japan; also N Africa, Middle East, C Asia, Sub-Himalayan zone, S India, Sri Lanka, C, E & S China, Taiwan, Indochina, and Sumatra.
Subspecies and Distribution. C. lupus Linnaeus, 1758 - Asia, Europe. C. l. albus Kerr, 1792 — N Russia. C. l. arctos Pocock, 1935 — Canadian High Arctic. C. l. baileyi Nelson & Goldman, 1929 — Mexico, SW USA (extinct in the wild). C. l. communis Dwigubski, 1804 — C Russia. C. l. cubanensis Ognev, 1923 — E-C Asia. C. l. dingo Meyer, 1793 — SE Asia and Australasia. C. l. lycaon Schreber, 1775 — SE Canada, NE USA. C. l. nubilus Say, 1823 — E-C Canada and C USA. C. l. occidentalis Richardson, 1829 — Alaska, NW Canada. C. l. pallipes Sykes, 1831 — Middle East and SW Asia to India. in Canidae
Subspecies and Distribution. C. lupus Linnaeus, 1758 - Asia, Europe. C. l. albus Kerr, 1792 — N Russia. C. l. arctos Pocock, 1935 — Canadian High Arctic. C. l. baileyi Nelson & Goldman, 1929 — Mexico, SW USA (extinct in the wild). C. l. communis Dwigubski, 1804 — C Russia. C. l. cubanensis Ognev, 1923 — E-C Asia. C. l. dingo Meyer, 1793 — SE Asia and Australasia. C. l. lycaon Schreber, 1775 — SE Canada, NE USA. C. l. nubilus Say, 1823 — E-C Canada and C USA. C. l. occidentalis Richardson, 1829 — Alaska, NW Canada. C. l. pallipes Sykes, 1831 — Middle East and SW Asia to India.
Subspecies and Distribution. L.t.tolaiPallas,1778—InnerMongolia(=NeiMongol),andGansu(NCChina). L.t.buchariensisOgnev,1922—TajikistanandNEAfghanistan. L.t.cheybaniBaloutch,1978—SWIran(ZagrosMts). L.t.cinnamomeusShamel,1940—SWSichuan,andNYunnan(SCChina). L.t.filchneriMatschie,1908—Shaanxi(CChina). L.t.lehmanniSevertzov,1873—SKazakhstan,Turkmenistan,andextremeN&NEIran,EtoSSiberia,Mongolia,andXinjiang(NWChina). L. t. swinhoei Thomas, 1894 — from Heilongjiang, Jilin, Liaoning, Inner Mongolia S to Hebei, Beijing, Henan, Shaanxi, Shanxi, and Shandong (NE & E China). The Tolai Hare occurs in the steppes E of the Caspian Sea, S to NE & SW Iran, E through the Middle Asian republics to Afghanistan, and from Kazakhstan and S Siberia to Mongolia, S Russian Far East, NW, C & NE China; an isolated population lives in S Iraq and SW Iran. A single specimen in South Asia might extend the distribution of the Tolai Hare as far S as Jammu and Kashmir, N India. in Leporidae
Subspecies and Distribution. L.t.tolaiPallas,1778—InnerMongolia(=NeiMongol),andGansu(NCChina). L.t.buchariensisOgnev,1922—TajikistanandNEAfghanistan. L.t.cheybaniBaloutch,1978—SWIran(ZagrosMts). L.t.cinnamomeusShamel,1940—SWSichuan,andNYunnan(SCChina). L.t.filchneriMatschie,1908—Shaanxi(CChina). L.t.lehmanniSevertzov,1873—SKazakhstan,Turkmenistan,andextremeN&NEIran,EtoSSiberia,Mongolia,andXinjiang(NWChina). L. t. swinhoei Thomas, 1894 — from Heilongjiang, Jilin, Liaoning, Inner Mongolia S to Hebei, Beijing, Henan, Shaanxi, Shanxi, and Shandong (NE & E China). The Tolai Hare occurs in the steppes E of the Caspian Sea, S to NE & SW Iran, E through the Middle Asian republics to Afghanistan, and from Kazakhstan and S Siberia to Mongolia, S Russian Far East, NW, C & NE China; an isolated population lives in S Iraq and SW Iran. A single specimen in South Asia might extend the distribution of the Tolai Hare as far S as Jammu and Kashmir, N India.
FIGURE 15 in New species and records of Hygrodromicus Tronquet, 1981 and Paratrichodromeus Zerche, 1992 from the Middle Asia, the Himalayan Region and China (Coleoptera: Staphylinidae: Omaliinae: Anthophagini)
FIGURE 15. Distribution of Paratrichodromeus in Central Asia: P. angustilobatus (triangle), P. punctulatus (circles), P. sukranensis (squares).
FIGURES 12–14 in New species and records of Hygrodromicus Tronquet, 1981 and Paratrichodromeus Zerche, 1992 from the Middle Asia, the Himalayan Region and China (Coleoptera: Staphylinidae: Omaliinae: Anthophagini)
FIGURES 12–14. Habitus of Paratrichodromeus: 12—P. angustilobatus (holotype), 13—P. punctulatus (Tajikistan, Hissar Mts.), 14—P. sukranensis (Kyrgyzstan, Trans-Alay Range). Scale bars: 1.0 mm.
FIGURES 6–11 in New species and records of Hygrodromicus Tronquet, 1981 and Paratrichodromeus Zerche, 1992 from the Middle Asia, the Himalayan Region and China (Coleoptera: Staphylinidae: Omaliinae: Anthophagini)
FIGURES 6–11. Aedeagus of Hygrodromicus (Figs. 6–7: H. klapperichi, Figs. 8–9: H. latilobatus (holotype)) and Paratrichodromeus (Figs. 10–11: P. angustilobatus): 6, 8, 10—parameral view, 7, 9, 11—lateral view. Scale bar: 0.1 mm.
FIGURES 1–5 in New species and records of Hygrodromicus Tronquet, 1981 and Paratrichodromeus Zerche, 1992 from the Middle Asia, the Himalayan Region and China (Coleoptera: Staphylinidae: Omaliinae: Anthophagini)
FIGURES 1–5. Habitus: 1—Geodromicus palpalis (paratype), 2—Hygrodromicus klapperichi (Afghanistan), 3—H. latilobatus (holotype), 4—H. reitteri (Kyrgyzstan, Issyk Kul), 5—H. wrasei (Tajikistan, Hissar Mts.). Scale bar: 1.0 mm.
FIGURE 3 in DNA analysis of a non-native lineage of Sinanodonta woodiana species complex (Bivalvia: Unionidae) from Middle Asia supports the Chinese origin of the European invaders
FIGURE 3. Shell of a specimen of Sinanodonta cf. gibba (Benson in Cantor, 1842) from the Amu Darya River. Scale bar = 3 cm. (Photo: Ekaterina Konopleva).
FIGURE 5 in DNA analysis of a non-native lineage of Sinanodonta woodiana species complex (Bivalvia: Unionidae) from Middle Asia supports the Chinese origin of the European invaders
FIGURE 5. Majority-rule consensus Bayesian phylogenetic tree based on the COI haplotypes of Sinanodonta spp. and related taxa. Numbers close to nodes are Bayesian posterior probabilities. The scale bar indicates the branch length.
FIGURE 4 in DNA analysis of a non-native lineage of Sinanodonta woodiana species complex (Bivalvia: Unionidae) from Middle Asia supports the Chinese origin of the European invaders
FIGURE 4. Median-joining network of the COI sequences of Sinanodonta cf. gibba (Benson in Cantor, 1842) (N = 53; list of additional sequences in Appendix 1). The red numbers near branches indicate the numbers of nucleotide substitutions between haplotypes. Size of circles corresponds to the number of available sequences for each haplotype (smallest circle = 1 sequence).
FIGURE 2 in DNA analysis of a non-native lineage of Sinanodonta woodiana species complex (Bivalvia: Unionidae) from Middle Asia supports the Chinese origin of the European invaders
FIGURE 2. Habitat of Sinanodonta cf. gibba (Benson in Cantor, 1842) from Uzbekistan: a floodplain lake of the Amu Darya River near the town of Xonqa. (Photo: Alexey Chernyak).
FIGURE 1 in DNA analysis of a non-native lineage of Sinanodonta woodiana species complex (Bivalvia: Unionidae) from Middle Asia supports the Chinese origin of the European invaders
FIGURE 1. Distribution range of Sinanodonta cf. gibba (Benson in Cantor, 1842) in Uzbekistan. The red circle indicates our sequenced record from the Amu Darya River and the blue circles indicate published records (Appendix 2). The color hatching indicates the corresponding river drainage basins.
FIGURES 50-53. Female genitalia. 50 in An integrative taxonomic revision of the genus Triphosa Stephens, 1829 (Geometridae: Larentiinae) in the Middle East and Central Asia, with description of two new species
FIGURES 50-53. Female genitalia. 50: paralectotype of Triphosa taochata, conspecific with T. dubitata (Achalzich, g. prep 2070/2016. H. Rajaei); 51: lectotype of Triphosa taochata (Hankynda, g. prep. 0020/2018 D. Wanke); 52: Triphosa taochata (Türkei, Erzurum, Tal des Coruh, 5.vii.2002, g. prep. 0034/2018 D. Wanke); 53: paralectotype of Hydria ravulata (Issyk-kul, g. prep. 0049/2018 D. Wanke). a = ventral view; b = lateral view.
FIGURES 46-49. Female genitalia. 46 in An integrative taxonomic revision of the genus Triphosa Stephens, 1829 (Geometridae: Larentiinae) in the Middle East and Central Asia, with description of two new species
FIGURES 46-49. Female genitalia. 46: Triphosa dubitata (Italy, Trafoi, 15.vi.1927, g. prep. 0013/2018 D. Wanke); 47: Triphosa silviae sp. n. (Iran, Kohkiluyeh-va-Boyerahmad, 24.v.2009, g. prep 0009/2018 D. Wanke); 48: Triphosa lecerfi sp. n. (Kyrgyzstan, Alai, Dugoba riv., 27.vii.1993, g. prep. 0041/2018 D. Wanke); 49: Triphosa sabaudiata (Switzerland, Preda, g. prep 0001/2018 D. Wanke). a = ventral view; b = lateral view.
FIGURES 44-45. Male genitalia. 44 in An integrative taxonomic revision of the genus Triphosa Stephens, 1829 (Geometridae: Larentiinae) in the Middle East and Central Asia, with description of two new species
FIGURES 44-45. Male genitalia. 44: Hydria cervinalis (Germany, Heidelberg, 29.iii.1974, g. prep. 0051/2018 D. Wanke); 45: lectotype of Hydria ravulata (Issyk-kul, g. prep. 0048/2018 D. Wanke). a = genitalia capsule; b = aedeagus.
FIGURES 41-43. Male genitalia. 41 in An integrative taxonomic revision of the genus Triphosa Stephens, 1829 (Geometridae: Larentiinae) in the Middle East and Central Asia, with description of two new species
FIGURES 41-43. Male genitalia. 41: Triphosa sabaudiata (Germany, Gempen, i.1959, g. prep. 0052/2018 D. Wanke); 42: holotype of Triphosa agnata syn. n. (Turkey, Cesarée, g. prep. 223); 43: Triphosa taochata (Turkey, Artvin, Tekkale near Yusufeli, 13.iv.2002, g. prep. 0033/2018 D. Wanke). a = genitalia capsule; b = aedeagus.
FIGURE 54 in An integrative taxonomic revision of the genus Triphosa Stephens, 1829 (Geometridae: Larentiinae) in the Middle East and Central Asia, with description of two new species
FIGURE 54. Un-rooted neighbour joining tree (Saitou & Nei 1987) based on 14 species of the genus Triphosa (calculated using K2P model: Kimura 1980 with MEGA7 (Kumar et al. 2016). Black arrows indicate the female lecto- and paralectotype of Triphosa taochata (the female paralectotype specimen that clustered with Triphosa dubitata has also dubitata genitalia pattern (see figs 46, 50); the female lectotype specimen that clustered with specimens from the Middle East has taochata genitalia pattern (see figs 51, 52).
FIGURES 38-40. Male genitalia. 38 in An integrative taxonomic revision of the genus Triphosa Stephens, 1829 (Geometridae: Larentiinae) in the Middle East and Central Asia, with description of two new species
FIGURES 38-40. Male genitalia. 38: Triphosa dubitata (Georgia, Borjomi, 22.vii.2006, g. prep. 0016/2018 D. Wanke); 39: Triphosa silviae sp. n. (Khorasan, Kopedagh-Allahakbar, 16.vi.1974, g. prep. 0008/2018 D. Wanke); 40: Triphosa lecerfi sp. n. (Kirghizia, Alay range, Dugoba riv., 15.vii.1995, g. prep. 0039/2018 D). a = genitalia capsule; b = aedeagus.
FIGURES 13-17 in An integrative taxonomic revision of the genus Triphosa Stephens, 1829 (Geometridae: Larentiinae) in the Middle East and Central Asia, with description of two new species
FIGURES 13-17. Diagnostic characters of the genitalia of Triphosa species (ventral view). 13: Triphosa dubitata; 14: Triphosa silviae sp. n.; 15: Triphosa lecerfi sp. n.; 16: Triphosa sabaudiata; 17: Triphosa taochata; a = socii; b = labides; c = sacculus projections (unspread, in natural position).
FIGURES 1-5 in An integrative taxonomic revision of the genus Triphosa Stephens, 1829 (Geometridae: Larentiinae) in the Middle East and Central Asia, with description of two new species
FIGURES 1-5. Wing venation in genus Triphosa and its closely related genera. 1: Triphosa dubitata, with two areoles. 2: Philereme transversata; 3: Pareulype berberata; 4: Rheumaptera hastata; 5: Hydria cervinalis. Areoles marked with grey in 2– 5. Only one areole is present in Rheumaptera.
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