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333 results for “Kyrgyzstan”
FIGURES 79–86 in World catalogue of the genus Cossulus Staudinger, 1887 (Lepidoptera, Cossidae) with description of Cossulus irtlachi sp. nov. from Kyrgyzstan
FIGURES 79–86. Maps of distribution: 79. C. intractatus; 80. C. irani; 81. C. irtlachi; 82. C. issycus; 83. C. kabulense; 84. C. lena; 85. C. lignosus; 86. C. mollis.
FIGURES 1–5 in A new species of Lathrobium from Kyrgyzstan (Coleoptera, Staphylinidae: Paederinae)
FIGURES 1–5. Lathrobium lackneri: 1—forebody; 2—head and pronotum; 3—elytra; 4—male sternite VII; 5—male sternite VIII (slightly damaged). Scale bars: 1.0 mm.
FIGURES 6–10 in A new species of Lathrobium from Kyrgyzstan (Coleoptera, Staphylinidae: Paederinae)
FIGURES 6–10. Lathrobium lackneri: 6–7—aedeagus in lateral and in ventral view; 8—apex of ventral process of aedeagus in lateral view; 9—apex of ventral process of aedeagus in ventral view; 10—apex of dorsal plate and internal structures in lateral view. Scale bars: 6–7: 1.0 mm; 8–10: 0.2 mm.
FIGURES 1–6 in New herb gall wasps (Hymenoptera: Cynipidae: Aulacideini) from Kyrgyzstan, with description of a new genus and a review of the genus Panteliella Kieffer, 1901
FIGURES 1–6. Soparia oshensis Nastasi gen. and sp. nov. All images show holotype female INHS Insect Collection 288148. (1) Lateral habitus. (2) Head in anterior view; dotted line indicates ventral margin of clypeus. (3) Mesoscutum in dorsal view. (4) Scutellum in dorsal view. (5) Mesopleuron in lateral view. (6) Wings.
FIGURES 15–21 in New herb gall wasps (Hymenoptera: Cynipidae: Aulacideini) from Kyrgyzstan, with description of a new genus and a review of the genus Panteliella Kieffer, 1901
FIGURES 15–21. Isocolus barakus Nastasi sp. nov. All images show holotype female INHS Insect Collection 288135. (9) Lateral habitus. (10) Head in anterior view; dotted line indicates ventral margin of clypeus. (11) Pronotum in anterior view; arrows indicate conspicuously defined range of pronotal lateral suture. (12) Proximal antennomeres. (13) Mesopleuron in lateral view. (14) Mesoscutum in dorsal view. (15) Scutellum in dorsal view; posterior scutellum (partially covered by wings and thus clouded posteriorly in image).
FIGURES 9–14 in New herb gall wasps (Hymenoptera: Cynipidae: Aulacideini) from Kyrgyzstan, with description of a new genus and a review of the genus Panteliella Kieffer, 1901
FIGURES 9–14. Panteliella rugosa Nastasi sp. nov. All images show holotype female INHS Insect Collection 288137. (9) Lateral habitus. (10) Head in anterior view; dotted line indicates ventral margin of clypeus. (11) Mesoscutum in dorsal view. (12) Scutellum in dorsal view. (13) Mesopleuron in lateral view. (14) Fore wing.
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.
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest. in Suidae
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest.
Figure 7 in A chroniosuchid from the Triassic of Kyrgyzstan and analysis of chroniosuchian relationships
Figure 7. Alternative hypotheses of chroniosuchian relationships and their support by different sets of characters. Undisputed synapomorphy = black square, ambiguous synapomorphy = grey square, plesiomorphy = grey circle.
Figure 5 in A chroniosuchid from the Triassic of Kyrgyzstan and analysis of chroniosuchian relationships
Figure 5. Strict consensus of 16 most parsimonious trees. Numbers of characters supporting nodes mapped onto each node, with their status as indicated by PAUP abbreviated as follows: A, undisputed apomorphy; E, equivocal; U, unequivocal.
Figure 4 in A chroniosuchid from the Triassic of Kyrgyzstan and analysis of chroniosuchian relationships
Figure 4. Paratype specimens of Madygenerpeton pustulatus sp. nov. A, FG 596/V/6, a single osteoderm, in dorsal view; B, FG 596/V/5, a series of five osteoderms (numbers from cranial to caudal), in ventral view. Greyshaded: ventral-facing sides of the ventral osteoderm processes. Abbreviations: aa, ala anterior; csve, crista scutulumi ventralis externa; paf, posterior articulation face of the outer osteoderm wing; pap, process of the articular plate; pv, processus ventralis. Scale bars = 1 cm. ·
Figure 3 in A chroniosuchid from the Triassic of Kyrgyzstan and analysis of chroniosuchian relationships
Figure 3. Skull roof of Madygenerpeton pustulatus sp. nov. (reconstruction). A, with ornament on left side and ridges on right side (dorsal view); B–D, diagrammatic reconstruction (B, dorsal; C, ventral; D, lateral). Abbreviations: ec, ectopterygoid; f, frontal; ju, jugal; la, lacrimal; m, maxilla; n, nasal; na, naris; or, orbit; p, parietal; pl, palatine; pm, premaxilla; po, postorbital; pof, postfrontal; pp, postparietal; pp-em, postparietal embayment; prf, prefrontal; pro, preorbital fenestra; ps, parasphenoid; pt, pterygoid; qj, quadratojugal; sq, squamosal; sq-em, squamosal embayment; st, supratemporal; stf, subtemporal fenestra; ta, tabular.
Figure 1. A in A chroniosuchid from the Triassic of Kyrgyzstan and analysis of chroniosuchian relationships
Figure 1. A, location in Inner Asia; B, close-up on west Kyrgyzstan region; C, diagrammatic map showing the stratotype exposures of the Madygen Formation and the type locality of Madygenerpeton.
Figure 2 in A chroniosuchid from the Triassic of Kyrgyzstan and analysis of chroniosuchian relationships
Figure 2. Holotype specimen of Madygenerpeton pustulatus sp. nov. A–C, dorsal view; D–F, ventral view. Abbreviations: ec, ectopterygoid; f, frontal; ju, jugal; la, lacrimal; m, maxilla; n, nasal; na, naris; or, orbit; p, parietal; pin, pineal foramen; pl, palatine; pm, premaxilla; po, postorbital; pof, postfrontal; pp, postparietal; pp-em, postparietal embayment; prf, prefrontal; pro, preorbital fenestra; sa, surangular; sq, squamosal; sq-em, squamosal embayment; st, supratemporal; ta, tabular.
Distribution. SW Kazakhstan, Turkmenistan, NE Iran, SE Uzbekistan, Kyrgyzstan, Tajikistan, N Afghanistan, N Pakistan, and NW India. in Vespertilionidae
Distribution. SW Kazakhstan, Turkmenistan, NE Iran, SE Uzbekistan, Kyrgyzstan, Tajikistan, N Afghanistan, N Pakistan, and NW India.
Subspecies and Distribution. E.g.gobiensisBobrinski,1926—SKazakhstan,Kyrgyzstan,Tajikistan,SRussia(Tuva),W&SMongolia,NW&NChina,NEAfghanistan,NPakistan(Gilgitarea),andIndia(recordofuncertainidentity);thereisadubiousreportfromNepal. E. g. bobrinskoi Kuzyakin, 1935 — W & C Kazakhstan and NW Iran. in Vespertilionidae
Subspecies and Distribution. E.g.gobiensisBobrinski,1926—SKazakhstan,Kyrgyzstan,Tajikistan,SRussia(Tuva),W&SMongolia,NW&NChina,NEAfghanistan,NPakistan(Gilgitarea),andIndia(recordofuncertainidentity);thereisadubiousreportfromNepal. E. g. bobrinskoi Kuzyakin, 1935 — W & C Kazakhstan and NW Iran.
Subspecies and Distribution. E.s.serotinusSchreber,1774—muchofEuropeexceptforSIberianPeninsulaandmostofScandinavia,beingfoundinSBritainandfromN&CIberianPeninsulaEtoextremeSScandinavia,SWEuropeanRussia,Caucasus,andN&ETurkeyalongwithnumerousMediterraneanIs(BalearicIs,Corsica,Sardinia,andSicily),includingIonian(Corfu)andAegeanIs(Samothrace,Lesbos,Skyros,Euboea,Samos,Crete,andRhodes). E.s.mirzadeFilippi,1865—STurkey,WSyria,Lebanon,Israel,andNW,C&SWIran. E. s. turcomanus Eversmann, 1840 — Central Asia in SC Russia, Kazakhstan, Uzbekistan, Turkmenistan, N Iran, Kyrgyzstan, Tajikistan, N Afghanistan, and NW China (Xinjiang). in Vespertilionidae
Subspecies and Distribution. E.s.serotinusSchreber,1774—muchofEuropeexceptforSIberianPeninsulaandmostofScandinavia,beingfoundinSBritainandfromN&CIberianPeninsulaEtoextremeSScandinavia,SWEuropeanRussia,Caucasus,andN&ETurkeyalongwithnumerousMediterraneanIs(BalearicIs,Corsica,Sardinia,andSicily),includingIonian(Corfu)andAegeanIs(Samothrace,Lesbos,Skyros,Euboea,Samos,Crete,andRhodes). E.s.mirzadeFilippi,1865—STurkey,WSyria,Lebanon,Israel,andNW,C&SWIran. E. s. turcomanus Eversmann, 1840 — Central Asia in SC Russia, Kazakhstan, Uzbekistan, Turkmenistan, N Iran, Kyrgyzstan, Tajikistan, N Afghanistan, and NW China (Xinjiang).
Distribution. Georgia, Armenia, Azerbaijan, NW & NE Iran, S Kazakhstan, Uzbekistan, Turkmenistan, W Kyrgyzstan, Tajikistan, NW Afghanistan, N Pakistan, and NW India (Jammu and Kashmir). in Vespertilionidae
Distribution. Georgia, Armenia, Azerbaijan, NW & NE Iran, S Kazakhstan, Uzbekistan, Turkmenistan, W Kyrgyzstan, Tajikistan, NW Afghanistan, N Pakistan, and NW India (Jammu and Kashmir).
Subspecies and Distribution. N. n. noctula Schreber, 1774 — throughout Europe from Great Britain, France, and Spain E to W Russia, W Kazakhstan, and SW Turkmenistan, including S Scandinavia, Gotland and Oland Is, and Cyprus (Cyprus records somewhat tentatively regarded as this subspecies). Absent throughout much of Iberia and is locally extinct in Portugal. N. n. lebanoticus D. L.. Harrison, 1962 — WC & SW Syria, Lebanon, and NE Israel. N. n. mecklenburzevi Kuzyakin, 1934 — SC & E Kazakhstan, SC Russia, W Uzbekistan, Tajikistan, Kyrgyzstan, and NW China (Xinjiang). The species may be present in N Africa, with two records claimed from Algeria in 1858, but these may represent N. lasiopterus; further sampling is needed. in Vespertilionidae
Subspecies and Distribution. N. n. noctula Schreber, 1774 — throughout Europe from Great Britain, France, and Spain E to W Russia, W Kazakhstan, and SW Turkmenistan, including S Scandinavia, Gotland and Oland Is, and Cyprus (Cyprus records somewhat tentatively regarded as this subspecies). Absent throughout much of Iberia and is locally extinct in Portugal. N. n. lebanoticus D. L.. Harrison, 1962 — WC & SW Syria, Lebanon, and NE Israel. N. n. mecklenburzevi Kuzyakin, 1934 — SC & E Kazakhstan, SC Russia, W Uzbekistan, Tajikistan, Kyrgyzstan, and NW China (Xinjiang). The species may be present in N Africa, with two records claimed from Algeria in 1858, but these may represent N. lasiopterus; further sampling is needed.
FIGURES 1–6. Scoparia juldusellus. 1 in Scoparia juldusellus (Caradja, 1916), a little-known snout moth species new to the fauna of Kyrgyzstan (Lepidoptera: Crambidae: Scopariinae)
FIGURES 1–6. Scoparia juldusellus. 1—male, Kara-Buura River valley; 2—male, Dolon Pass; 3—male genitalia, Kara-Buura valley, ventral view (aedeagus removed); 4—the same, aedeagus; 5, 6—habitats in Kyrgyzstan (5—Dolon Pass, Inner Tien-Shan; 6—Kara-Buura River valley, West Tien-Shan).
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