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FIGURE 5 in Mites of the families Neopygmephoridae and Scutacaridae associated with variegated mud-loving beetles (Coleoptera: Heteroceridae) from Russia and Kazakhstan

FIGURE 5. Allopygmephorus spinisetus sp. nov., female: A—right leg I in dorsal view, B—right leg II in dorsal view.

FIGURE 3 in A stonefly species extinct in Europe (Taeniopteryx araneoides Klapalek, 1902, Taeniopterygidae, Plecoptera) is thriving in the Irtysh River in West Siberia and North Kazakhstan

FIGURE 3. Detail of a female of Taeniopteryx araneoides from Omsk, 3 v 2003: a—wings; b—end of abdomen in dorsoposterior view; d—the same, ventral view; scale bar 1 mm.

FIGURE 2 in A stonefly species extinct in Europe (Taeniopteryx araneoides Klapalek, 1902, Taeniopterygidae, Plecoptera) is thriving in the Irtysh River in West Siberia and North Kazakhstan

FIGURE 2. Details of Taeniopteryx araneoides males from Omsk, 3 v 2003: a–e—mature male, f—male with a not yet fully expanded epiproct; a—general habitus; b—wings; c—end of abdomen in lateral view; d—the same, dorsal view; e—the same, ventral view; f—laterodorsal view; scale bar 1 mm.

FIGURE 1 in A stonefly species extinct in Europe (Taeniopteryx araneoides Klapalek, 1902, Taeniopterygidae, Plecoptera) is thriving in the Irtysh River in West Siberia and North Kazakhstan

FIGURE 1. Taeniopteryx araneoides photographed at the Irtysh River in the Omsk centre: a—males on driftwood (two not fully mature with grey legs and a mature one with black legs), 29 iv 2006; b—female, 4 v 1979; c—attempt at mating of teneral male and a female with crumpled wings, 4 v 1979.

FIGURES 54–57 in Three new species and one new subspecies of Deserticossus Yakovlev, 2006 (Lepidoptera: Cossidae) from Kazakhstan, Kyrgyzstan and Russia, with world catalogue of the genus

FIGURES 54–57. Deserticossus, genitalia: 54. D. doroshkini, ♂, holotype; 55. D. kamelini, ♂, holotype, GenPr MWMW: 25.259; 56. D. selevini, ♂, holotype; 57. D. kamelini, ♀, paratype, GenPr MWMW: 30.892.

FIGURES 39–53 in Three new species and one new subspecies of Deserticossus Yakovlev, 2006 (Lepidoptera: Cossidae) from Kazakhstan, Kyrgyzstan and Russia, with world catalogue of the genus

FIGURES 39–53. Deserticossus, adult specimens: 43. D. sareptensis, ♂, holotype (BMNH); 44. D. tsingtauana, ♂, cotype (MHUB); 45. D. tsingtauana, ♂, Korea, N. Myohyangsan, 15.06.1985, leg. Hevelka (MWM); 46. D. tsingtauana, ♂, [Russia], Fare East, Primorye, Pogranitschnyi, 60 km SW lake Chanka, 10–20.07.1992, 44°25' N, 131°24' E, ex coll. A. Schitlmeister (MWM); 47. D. tsingtauana, ♀, [Russia], Ussuri reg., Ussurijsk, Kajmanovka, 5.08.1964, A. Tzvetaev leg., F. Daniel coll. (MWM); 48. D. tsingtauana didenkoi, paratype, ♂, Mongolia, Central Aimak, 25 km W Erdennesant, 47°22′ N / 104°13′ E,14¯15.05.2003, 1260 m, leg. A. Saldaitis (MWM); 49. D. volgensis, ♀, holotype (ZISP); 50. D. volgensis, ♂, Süd. Russl[and]. (MWM); 51. D. volgensis, ♀, Ros. Mer., Sarepta (MWM); 52. D. selevini, ♂, holotype, underside (ZISP); 53. D. beketi, ♂, paratype, underside (RYB).

FIGURES 24–38 in Three new species and one new subspecies of Deserticossus Yakovlev, 2006 (Lepidoptera: Cossidae) from Kazakhstan, Kyrgyzstan and Russia, with world catalogue of the genus

FIGURES 24–38. Deserticossus, adult specimens: 29. D. decoratus, ♂, holotype (MWM); 30. D. decoratus, ♀, paratype (MWM); 31. D. janychar, ♂, holotype (MWM); 32. D. lukhtanovi, ♂, holotype (MWM); 33. D. lukhtanovi, ♂, paratype, Tadzhikistan, Turkestanskii Mts., 55 km S. Ura-Tyube, Obburdon-pass, 14.–16.07.1994, 3000–3500 m, leg. Lukhtanov (MWM); 34. D. mongoliana, ♂, paratype, Mongolia, Gobi Altai aimak, Baga nuuryn nurd els, an der SO-Ecke des Sees Döröö nuur, ca. 1200 m, 12.7.66 (MWM); 35. D. mongoliana, ♀, allotype, Mongolia, Ostgobi aimak, Cagan Elis, 30 km OSO von Zuun-Bajan, 800 m, 22.6.63 (MWM); 36. D. murinus, ♂, holotype (BMNH); 37. D. murinus, ♂, Kazakhstan, Taldy-Kurgan, Ili Fluss, Borochudschir, 500 m, 7–12.06.1996, leg. V. Lukhtanov (MWM); 38. D. murinus, ♀, Kazakhstan, Taldy-Kurgan, Ili Fluss, Borochudschir, 500 m, 7–12.06.1996, leg. V. Lukhtanov (MWM). 39. D. praeclarus, ♂, holotype (MHUB); 40. D. pulverulentus, ♂, cotype (MHUB); 41. D. pulverulentus, ♂, Transcasp., Repetek, 30.04.1966, leg. Tzvetaev A. (MWM); 42. D. pulverulentus, ♀, Turkmenistan, Chardzhou, 4.05.1995 (MWM)

FIGURES 9–23 in Three new species and one new subspecies of Deserticossus Yakovlev, 2006 (Lepidoptera: Cossidae) from Kazakhstan, Kyrgyzstan and Russia, with world catalogue of the genus

FIGURES 9–23. Deserticossus, adult specimens: 9. D. arenicola arenicola, ♂, lectotype (MHUB); 10. D. arenicola arenicola, ♂, holotype of Holcocerus dilutior Rothschild, 1912 (BMNH); 11. D. arenicola arenicola, ♂, Uzbekistan, Ghissar Mts., Jurgy, 1000 m, 1.07.1994, leg. V. Lukhtanov (MWM); 12. D. arenicola arenicola, ♀, S. Kazakhstan, Syr-Darja Fluss, 50 km W Aris', 23¯24.05.1996, leg. V. Lukhtanov (MWM); 13. D. arenicola iranicus, ♀, holotype (BMNH); 14. D. arenicola iranicus, ♂, Iran, Baloutchistan, Strasse Knach-Zahedan, Fort Sengan, 1800 m, 1938, coll. Brandt (MWM); 15. D. arenicola transcaucasicus, ♂, lectotype (MWM); 16. D. arenicola transcaucasicus, ♀, paralectotype (RMNH); 17. D. beketi, ♂, paratype (RYB); 18. D. campicola, ♂, lectotype (ZISP); 19. D. campicola, ♂, USSR, Uzbekistan, Mt. Tian-Shan, Bolshoi Tschimgan, 1600 m, 23–28.06.1980, K. & L. Krusek leg. (MWM); 20. D. campicola, ♀, Turkestan [S. Kazakhstan], Syr-Darja, Perowsk [Kyzylorda], coll. Wagner (MWM); 21. D. churkini, ♂, holotype (MWM); 22. D. consobrinus, ♂, holotype (MHUB); 23. D. consobrinus, ♂, holotype of Cossus aksuensis Daniel, 1953 (MWM); 24. D. consobrinus, ♂, holotype of Holcocerus sheljuzhkoi Schawerda, 1930 (MNHW); 25. D. consobrinus, ♂, Ost-Turkestan [NW China], Chamil-Hami, Rückbeil, 1908 (MWM); 26. D. consobrinus, ♀, Ost-Turkestan [NW China], Chamil-Hami, Rückbeil, 1908 (MWM); 27. D. curdus, ♂, holotype (MWM); 28. D. danilevskyi, ♂, holotype (MWM).

FIGURES 1–8 in Three new species and one new subspecies of Deserticossus Yakovlev, 2006 (Lepidoptera: Cossidae) from Kazakhstan, Kyrgyzstan and Russia, with world catalogue of the genus

FIGURES 1–8. Deserticossus, type specimens: 1. D. doroshkini, ♂, holotype (ZISP); 2. D. doroshkini paratype, ♀ (RYB); 3. D. kamelini, ♂, holotype (MWM); 4. D. kamelini, paratype, ♀ (MWM); 5. D. selevini, ♂, holotype (ZISP); 6. D. selevini, paratype, ♂, Kazakhstan, Nurly env., 25.06.2002, leg. Lind (MWM); 7. D. tsingtauana didenkoi, ♂, holotype (ZISP); 8. D. tsingtauana didenkoi, paratype, ♂, Mongolia, Central Aimak, 25 km W Erdennesant, 47°22′ N / 104°13′ E,14¯15.05.2003, 1260 m, leg. A. Saldaitis (MWM).

opencc-zeroFeb 2024View details →

Supplementary material 2 from: Kubentayev SA, Alibekov DT, Perezhogin YV, Lazkov GA, Kupriyanov AN, Ebel AL, Izbastina KS, Borodulina OV, Kubentayeva BB (2024) Revised checklist of endemic vascular plants of Kazakhstan. PhytoKeys 238: 241-279. https://doi.org/10.3897/phytokeys.238.114475

Former endemics of Kazakhstan that are now reclassified as synonyms for species exhibiting broader geographical distributions

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).

Subspecies and Distribution. V. ¢. corsac Linnaeus, 1768 — N part of range to pre-Altai steppe. Vc. kalmykorum Ognev, 1935 — Volgo-Ural steppes and Volga Basin. V. ¢. scorodumovi Dorogostaiski, 1935 — N China, Mongolia, and Russia (Transbaikalia). V. ¢. turemenicus Ognev, 1935 — plains of C Asia and N Afghanistan, NE Iran, and Kazakhstan. in Canidae

Subspecies and Distribution. V. ¢. corsac Linnaeus, 1768 — N part of range to pre-Altai steppe. Vc. kalmykorum Ognev, 1935 — Volgo-Ural steppes and Volga Basin. V. ¢. scorodumovi Dorogostaiski, 1935 — N China, Mongolia, and Russia (Transbaikalia). V. ¢. turemenicus Ognev, 1935 — plains of C Asia and N Afghanistan, NE Iran, and Kazakhstan.

Subspecies and Distribution. U. a. arctos Linnaeus, 1758 — Europe and W Russia. U. a. alascensis Merriam, 1896 — most of Alaska (excluding Alaska Peninsula, SE panhandle & Kodiak Island group). U. a. beringianus Middendorff, 1853 — NE Russia (Kamchatka Peninsula & N Kuril Islands northward through the Koryak Autonomous District, and along W coast of the Sea of Okhotsk). U. a. collaris Cuvier, 1824 — Russia (Siberia, from E of the Yenisey River to the Bering Sea, but excluding Kamchatka and more southern parts of the Russian Far East), N Mongolia. U. a. dalli Merriam, 1896 — SE Alaska (N of Alexander Archipelago). U. a. gyas Merriam, 1902 — Alaska peninsula. U. a. horribilis Ord, 1815 —W Canada (Yukon, North-West Territories, British Columbia & Alberta), inland W USA (extirpated from S Wyoming to Mexico). U. a. isabellinus Horsfield, 1826 — N India, Pakistan, Afghanistan, N to Kazakhstan and Mongolia (Gobi Desert). U. a. lasiotus Gray, 1867 — Russia (Southern Kuril Islands, Sakhalin, Ussuri/Amur river region of the Russian Far East), NE China, North Korea, and Japan (Hokkaido). U. a. middendorffi Merriam, 1896 — Alaska (Kodiak Island & nearby islands). U. a. pruinosus Blyth, 1853 — Tibetan Plateau, China, N Nepal. U. a. sitkensis Merriam, 1896 — SE Alaska (Alexander Archipelago & adjacent coastal area). U. a. stikeenensis Merriam, 1914 — W Canada (W British Columbia), and formerly W USA (W Washington and Oregon). U. a. syriacus Hemprich & Ehrenberg, 1828 — Middle East, from Turkey to Iran (extirpated in Syria), Caucasus mountains of Russia, Georgia, Armenia and Azerbaijan. in Ursidae

Subspecies and Distribution. U. a. arctos Linnaeus, 1758 — Europe and W Russia. U. a. alascensis Merriam, 1896 — most of Alaska (excluding Alaska Peninsula, SE panhandle & Kodiak Island group). U. a. beringianus Middendorff, 1853 — NE Russia (Kamchatka Peninsula & N Kuril Islands northward through the Koryak Autonomous District, and along W coast of the Sea of Okhotsk). U. a. collaris Cuvier, 1824 — Russia (Siberia, from E of the Yenisey River to the Bering Sea, but excluding Kamchatka and more southern parts of the Russian Far East), N Mongolia. U. a. dalli Merriam, 1896 — SE Alaska (N of Alexander Archipelago). U. a. gyas Merriam, 1902 — Alaska peninsula. U. a. horribilis Ord, 1815 —W Canada (Yukon, North-West Territories, British Columbia & Alberta), inland W USA (extirpated from S Wyoming to Mexico). U. a. isabellinus Horsfield, 1826 — N India, Pakistan, Afghanistan, N to Kazakhstan and Mongolia (Gobi Desert). U. a. lasiotus Gray, 1867 — Russia (Southern Kuril Islands, Sakhalin, Ussuri/Amur river region of the Russian Far East), NE China, North Korea, and Japan (Hokkaido). U. a. middendorffi Merriam, 1896 — Alaska (Kodiak Island & nearby islands). U. a. pruinosus Blyth, 1853 — Tibetan Plateau, China, N Nepal. U. a. sitkensis Merriam, 1896 — SE Alaska (Alexander Archipelago & adjacent coastal area). U. a. stikeenensis Merriam, 1914 — W Canada (W British Columbia), and formerly W USA (W Washington and Oregon). U. a. syriacus Hemprich & Ehrenberg, 1828 — Middle East, from Turkey to Iran (extirpated in Syria), Caucasus mountains of Russia, Georgia, Armenia and Azerbaijan.

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. V. p. peregusna Giildenstadt, 1770 — Russia. V. p. alpherakii Birula, 1910 — Afghanistan, Iran, Pakistan, Tajikistan, Turkmenistan, and Uzbekistan. V. p. euxina Pocock, 1936 — Bulgaria, Greece, Macedonia, Montenegro, Romania, Serbia, Turkey, and Ukraine. V. p. negans G. S. Miller, 1910 — NC & W China and S Mongolia. V.p. pallidior Stroganov, 1948 — Kazakhstan. V. p. syriaca Pocock, 1936 — Armenia, Azerbaidjan, Egypt, Georgia, Iraq, Israel, Lebanon, and Syria. in Mustelidae

Subspecies and Distribution. V. p. peregusna Giildenstadt, 1770 — Russia. V. p. alpherakii Birula, 1910 — Afghanistan, Iran, Pakistan, Tajikistan, Turkmenistan, and Uzbekistan. V. p. euxina Pocock, 1936 — Bulgaria, Greece, Macedonia, Montenegro, Romania, Serbia, Turkey, and Ukraine. V. p. negans G. S. Miller, 1910 — NC & W China and S Mongolia. V.p. pallidior Stroganov, 1948 — Kazakhstan. V. p. syriaca Pocock, 1936 — Armenia, Azerbaidjan, Egypt, Georgia, Iraq, Israel, Lebanon, and Syria.

Subspecies and Distribution. M..l. leucurus Hodgson, 1847 — C, E & S China.. M. l. amurensis Schrenck, 1859 — NE China (Manchuria), Kazakhstan, Mongolia, North and South Korea, and Russia (E of Volga River). in Mustelidae

Subspecies and Distribution. M..l. leucurus Hodgson, 1847 — C, E & S China.. M. l. amurensis Schrenck, 1859 — NE China (Manchuria), Kazakhstan, Mongolia, North and South Korea, and Russia (E of Volga River).

Subspecies and Distribution. M. c. capensis Schreber, 1776 — S Africa N to Angola, Mozambique, and Zambia. M. c. buechneri Baryshnikov, 2000 — C Asia including Afghanistan, Kazakhstan, Turkmenistan, and Uzbekistan. M. c. concisa Thomas & Wroughton, 1907 — Algeria, Morocco, and Subsaharan Africa from Mauritania to Ethiopia. M.c. cotton: Lydekker, 1906 — C Africa from Gabon to Tanzania. M. M.c. inaurita Hodgson, 1836 — Nepal. \g M.c. indica Kerr, 1792 — India and Pakistan. M. M.c. maxwell Thomas, 1923 — Kenya and Somalia. \J M.c. pumalio Pocock, 1946 — S Arabian Peninsula and Yemen. M. M.c. signata Pocock, 1909 — Guinea and Sierra Leone. \f M.c. wilsoni Cheesman, 1920 — Iran, Iraq, Israel, Jordan, Kuwait, Lebanon, Saudi Arabia, and Syria. in Mustelidae

Subspecies and Distribution. M. c. capensis Schreber, 1776 — S Africa N to Angola, Mozambique, and Zambia. M. c. buechneri Baryshnikov, 2000 — C Asia including Afghanistan, Kazakhstan, Turkmenistan, and Uzbekistan. M. c. concisa Thomas & Wroughton, 1907 — Algeria, Morocco, and Subsaharan Africa from Mauritania to Ethiopia. M.c. cotton: Lydekker, 1906 — C Africa from Gabon to Tanzania. M. M.c. inaurita Hodgson, 1836 — Nepal. \g M.c. indica Kerr, 1792 — India and Pakistan. M. M.c. maxwell Thomas, 1923 — Kenya and Somalia. \J M.c. pumalio Pocock, 1946 — S Arabian Peninsula and Yemen. M. M.c. signata Pocock, 1909 — Guinea and Sierra Leone. \f M.c. wilsoni Cheesman, 1920 — Iran, Iraq, Israel, Jordan, Kuwait, Lebanon, Saudi Arabia, and Syria.

opennotspecifiedAug 2011View details →

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.

opennotspecifiedDec 2021View details →

FIGURES 13–18 in Description of a new water mite species of the genus Lebertia Neuman, 1880 (Acari, Hydrachnidia: Lebertiidae) from Kazakhstan

FIGURES 13–18. Lebertia: 13, L. dmitrii, male (from Semenchenko & Tuzovskij 2010); 14-15, L. imamurai, female (from Imamura 1954); 16-18, L. convergella, female (from Tuzovskij 2004); 13, 14, 16, pedipalp; 17, P-3, medial view;18, chelicera.