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FIGURES 2–7. Repetekiodes spp. Adults. 2–4. R in Description of two new species of the genus Repetekiodes Amsel, 1961 (Lepidoptera: Pyralidae: Phycitinae) from Central Asia with faunal notes on the genus
FIGURES 2–7. Repetekiodes spp. Adults. 2–4. R. serratalis sp. nov. 2. Holotype, ♂, Kazakhstan. 3. Paratype, ♀, Kazakhstan. 4. Head laterally, paratype, ♂, Kazakhstan. 5–7. R. turanella sp. nov. 5. Paratype, ♂, Kazakhstan. 6. Paratype, ♀, Kazakhstan. 7. Head laterally, paratype, ♂, Kazakhstan.
FIGURE 1 in Description of two new species of the genus Repetekiodes Amsel, 1961 (Lepidoptera: Pyralidae: Phycitinae) from Central Asia with faunal notes on the genus
FIGURE 1. Neighbour Joining tree (K2P; constructed with MEGA11; COI 5'> 600 bp) including 12 sequences of Repetekiodes species, rooted with T. repetekella as outgroup. The scale bar represents 0.01 genetic difference.
FIGURES 14–15 in Description of two new species of the genus Repetekiodes Amsel, 1961 (Lepidoptera: Pyralidae: Phycitinae) from Central Asia with faunal notes on the genus
FIGURES 14–15. Repetekiodes spp. Female genitalia (paratypes, Kazakhstan). 14. R. serratalis sp. nov. (prep. № 3992). 15. R. turanella sp. nov. (prep. № 3999).
Distribution. Widespread in N and NE Africa, occurring from Senegal on the W coast of Africa to Egypt in the E, in a range that includes Morocco, Algeria, Tunisia, and Libya in the N to Nigeria, Chad, and Tanzania in the S. They have expanded their range from the Arabian Peninsula into Western Europe, to Bulgaria, Austria, and NE Italy and E into Turkey, Syria, Iraq, Iran, Central Asia, the entire Indian subcontinent, then E and S to Sri Lanka, Myanmar, Thailand, and parts of Indochina. in Canidae
Distribution. Widespread in N and NE Africa, occurring from Senegal on the W coast of Africa to Egypt in the E, in a range that includes Morocco, Algeria, Tunisia, and Libya in the N to Nigeria, Chad, and Tanzania in the S. They have expanded their range from the Arabian Peninsula into Western Europe, to Bulgaria, Austria, and NE Italy and E into Turkey, Syria, Iraq, Iran, Central Asia, the entire Indian subcontinent, then E and S to Sri Lanka, Myanmar, Thailand, and parts of Indochina.
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.
FIGS 3-10 in A new Eudorylas Aczél, 1940 from Central Asia (Diptera: Pipunculidae)
FIGS 3-10 Male genitalia of holotype of E. manasi sp. n. (3) Phallic guide, gonopods and hypandrium in ventral view. (4) Phallic guide and gonopods in lateral view from right side. (5) Phallus, sperm pump and ejaculatory apodeme in ventral view (one ejaculatory duct partly missing). (6) Syntergosternite 8 in caudal view. (7) Ejaculatory apodeme. (8) Right surstylus in lateral view. (9) Surstyli in strictly dorsal view. (10) Left surstylus in lateral view. Scale bars = 0.1 mm.
Distribution. Widespread in N and NE Africa, occurring from Senegal on the W coast of Africa to Egypt in the E, in a range that includes Morocco, Algeria, Tunisia, and Libya in the N to Nigeria, Chad, and Tanzania in the S. They have expanded their range from the Arabian Peninsula into Western Europe, to Bulgaria, Austria, and NE Italy and E into Turkey, Syria, Iraq, Iran, Central Asia, the entire Indian subcontinent, then E and S to Sri Lanka, Myanmar, Thailand, and parts of Indochina. in Canidae
Distribution. Widespread in N and NE Africa, occurring from Senegal on the W coast of Africa to Egypt in the E, in a range that includes Morocco, Algeria, Tunisia, and Libya in the N to Nigeria, Chad, and Tanzania in the S. They have expanded their range from the Arabian Peninsula into Western Europe, to Bulgaria, Austria, and NE Italy and E into Turkey, Syria, Iraq, Iran, Central Asia, the entire Indian subcontinent, then E and S to Sri Lanka, Myanmar, Thailand, and parts of Indochina.
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).
Insolation and CO2 impacts on the spatial differences of the MIS-9 and MIS-11 climate between monsoonal China and central Asia
<p>The model outputs we use are those performed in Yin & Berger (2012) where the climate of the last nine interglacials were simulated with the LOVECLIM model. The model outputs for MIS-11 and MIS-9 are used here to study the climate conditions in mid and eastern Asia.</p>
Subspecies and Distribution. M.c.coypusMolina,1782—Chilemainland. M.c.bonariensisE.GeoffroySaint-Hilaire,1805—Bolivia,Paraguay,NArgentina,SEBrazil,andUruguay. M.c.melanopsOsgood,1943—ChiloéI(CChile). M. c. santacruzae Hollister, 1914 — Argentina, from the Chaco S to Patagonia. Introduced widely into N South America, S North America, Europe, Central Asia, and East Africa. in Echimyidae
Subspecies and Distribution. M.c.coypusMolina,1782—Chilemainland. M.c.bonariensisE.GeoffroySaint-Hilaire,1805—Bolivia,Paraguay,NArgentina,SEBrazil,andUruguay. M.c.melanopsOsgood,1943—ChiloéI(CChile). M. c. santacruzae Hollister, 1914 — Argentina, from the Chaco S to Patagonia. Introduced widely into N South America, S North America, Europe, Central Asia, and East Africa.
Subspecies and Distribution. S.e.etruscusSavi,1822—EuropeandCaucasus;thissubspeciesprobablyalsoinTurkey(scatteredrecordsinW,N&SC). S.e.bactrianusStroganov,1958—Tajikistan. S.e.madagascariensisCoquerel,1848—Madagascar. S.e.micronyxBlyth,1855—Himalayas. S.e.nanulaStroganov,1941—Uzbekistan. S.e.nudipesBlyth,1855—NEIndia. S. e. perrottetti Duvernoy, 1842 — S India. Also known from Tenerife I, many Mediterranean Is, North Africa, Arabia, Socotra I, and Central and South-east Asia, but subspecies involved not known. in Soricidae
Subspecies and Distribution. S.e.etruscusSavi,1822—EuropeandCaucasus;thissubspeciesprobablyalsoinTurkey(scatteredrecordsinW,N&SC). S.e.bactrianusStroganov,1958—Tajikistan. S.e.madagascariensisCoquerel,1848—Madagascar. S.e.micronyxBlyth,1855—Himalayas. S.e.nanulaStroganov,1941—Uzbekistan. S.e.nudipesBlyth,1855—NEIndia. S. e. perrottetti Duvernoy, 1842 — S India. Also known from Tenerife I, many Mediterranean Is, North Africa, Arabia, Socotra I, and Central and South-east Asia, but subspecies involved not known.
FIGURES 99–102 in The genus Sphecodes Latreille 1804 (Hymenoptera: Apoidea: Halictidae) in Central Asia
FIGURES 99–102. Males, metasoma, T1–T3; 99—Sphecodes saxicolus Warncke; 100—S. schwarzi Astafurova & Proshchalykin; 101—S. haladai Warncke; 102—S. turanicus Astafurova & Proshchalykin, sp. nov.
FIGURES 88–92. 88 in The genus Sphecodes Latreille 1804 (Hymenoptera: Apoidea: Halictidae) in Central Asia
FIGURES 88–92. 88—male; 89–92—females; 88—metatibia; 89—thorax, ventral view; 90—antenna; 91, 92—hind wing; 88—Sphecodes spinulosus Hagens; 89—S. hyalinatus Hagens; 90—S. miniatus Hagens; 91—S. ephippius (Linné); 92—S. gibbus (Linnaeus).
FIGURES 76–81 in The genus Sphecodes Latreille 1804 (Hymenoptera: Apoidea: Halictidae) in Central Asia
FIGURES 76–81. Females; 76–79—mesoscutum; 80, 81—pronotum; 76—Sphecodes albilabris (Fabricius); 77—S. armeniacus Warncke; 78—S. intermedius Blüthgen; 79—S. pinguiculus Pérez; 80—S. ferruginatus Hagens; 81—S. pellucidus Smith.
FIGURES 70–75 in The genus Sphecodes Latreille 1804 (Hymenoptera: Apoidea: Halictidae) in Central Asia
FIGURES 70–75. Females, head: 70, 72–74 – dorsal view; 71, 75—lateral view; 70—Sphecodes spinulosus Hagens; 71—S. scabricollis Wesmael; 72—S. reticulatus Thomson; 73—S. intermedius Blüthgen; 74—S. gibbus (Linnaeus); 75—S. olivieri Lepeletier de Saint Fargeau.
FIGURES 64–69 in The genus Sphecodes Latreille 1804 (Hymenoptera: Apoidea: Halictidae) in Central Asia
FIGURES 64–69. Females, head; frontal view; 64—Sphecodes monilicornis (Kirby); 65—S. olivieri Lepeletier de Saint Fargeau; 66—S. rufiventris (Panzer); 67—S. saxicolus Warncke; 68—S. tadschicus Blüthgen; 69—S. schwarzi Astafurova & Proshchalykin.
FIGURES 58–63 in The genus Sphecodes Latreille 1804 (Hymenoptera: Apoidea: Halictidae) in Central Asia
FIGURES 58–63. Females, head; frontal view; 58—S. gibbus (Linnaeus); 59—S. anatolicus Warncke; 60— S. cristatus Hagens; 61—S. croaticus Meyer; 62—S. ephippius (Linné); 63—S. pellucidus Smith.
FIGURES 93–98 in The genus Sphecodes Latreille 1804 (Hymenoptera: Apoidea: Halictidae) in Central Asia
FIGURES 93–98. Males; 93, 94—head, frontal view; 95—head, dorsal view 96—mesoscutum; 97, 98—metasoma, T1–T2; 93—Sphecodes rufiventris (Panzer); 94—S. tadschicus Blüthgen; 95—S. puncticeps Thomson; 96—S. scabricollis Wesmael; 97—S. nurekensis Warncke; 98—S. croaticus Meyer.
FIGURE 104 in The genus Sphecodes Latreille 1804 (Hymenoptera: Apoidea: Halictidae) in Central Asia
FIGURE 104. Sphecodes turanicus Astafurova & Proshchalykin, sp. nov., male, paratype; a—lateral habitus; b—genital capsule; c—head, frontal view; d—head, dorsal view; e—mesoscutum.
FIGURES 2–28 in The genus Sphecodes Latreille 1804 (Hymenoptera: Apoidea: Halictidae) in Central Asia
FIGURES 2–28. Males, gonostylus, dorsal and lateral views; 2, 3—Sphecodes albilabris (Fabricius); 4, 5—S. anatolicus Warncke; 6, 7—S. crassus Thomson; 8, 9—S. cristatus Hagens; 10, 11—S. geoffrellus (Kirby); 12, 13—S. ferruginatus Hagens; 14, 15—S. gibbus (Linnaeus); 16, 17—S. armeniacus Warncke; 18, 19—S. ephippius (Linné); 20—S. croaticus Meyer; 21, 22—S. puncticeps Thomson; 23, 24—S. saxicolus Warncke; 25, 26—S. schwarzi Astafurova & Proshchalykin; 27, 28—S. pinguiculus Pérez. Scale bar: 0.5 mm.
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