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Fig. 4 in Estimating Migration of Gonioctena quinquepunctata (Coleoptera: Chrysomelidae) Inside a Mountain Range in a Spatially Explicit Context

Fig. 4. Principal component analysis (PCA) graph resulting from analyzing all SNPs from all sampled individuals. Each population is identified by a different color.

opennotspecifiedDec 2021View details →

Fig. 3 in Estimating Migration of Gonioctena quinquepunctata (Coleoptera: Chrysomelidae) Inside a Mountain Range in a Spatially Explicit Context

Fig. 3. Grids defining the spatially explicit context used in the coalescence models for simulating SNP data with PhyloGeoSim. Insects are absent from white cells but are potentially present in orange cells. Blue dots on the right grid (15,000 a—0) depict sampling locations.The left grid describes the spatial context assumed during the last glaciation.

Fig. 19 in A new species of the genus Bembecia Hübner, 1819 ["1816"](Lepidoptera: Sesiidae) from the Gissar Mountain Range

Fig. 19. The type locality of Bembecia sotchivkoi O. Gorbunov, sp.n.: Tajikistan, W Gissar Mts., upstream of Zambar River, Mura pass, ca. 3780 m, 05.VIII.2013. Photo by A. Sotchivko. Рис. 19. Типовое местонахождение Bembecia sotchivkoi O. Gorbunov, sp.n.: Таджикистан, Западный Гиссар, верховье реки Замбар, перевал Мура, около 3780 м, 05.VIII.2013. Фото А. Сочивко.

Figs 13–18 in A new species of the genus Bembecia Hübner, 1819 ["1816"](Lepidoptera: Sesiidae) from the Gissar Mountain Range

Figs 13–18. Genitalia of Bembecia sotchivkoi O. Gorbunov, sp.n.: 13–16 — paratype ♂. Genital preparation No OG–003-2022: 13 — tegumen-uncus complex; 14 — valva; 15 — saccus; 16 — phallus; 17–18 — paratype ♀. Genital preparation No OG–004-2022: 17 — common view; 18 — ostium bursae. Scale bar 0.5 mm for 1–11 and 0.25 mm for 12. Рис. 13–18. Гениталии Bembecia sotchivkoi O. Gorbunov, sp.n.: 13–16 — паратип ♂. Препарат гениталий № OG–003-2022: 13 — тегумен-ункусный комплекс; 14 — вальва; 15 — саккус; 16 — фаллюс; 17–18 — паратип ♀. Препарат гениталий № OG–004-2022: 17 — обЩий вид; 18 — устье копулЯтивной сумки. МасШтаб 0,5 мм длЯ 1–11 и 0,25 мм длЯ 12.

Figs 7–12. Bembecia spp. 7–10 — B in A new species of the genus Bembecia Hübner, 1819 ["1816"](Lepidoptera: Sesiidae) from the Gissar Mountain Range

Figs 7–12. Bembecia spp. 7–10 — B. senilis (Grum-Grshimailo, 1890): 7–8 — ♂, Kirgizstan, Transalai Mts., env. of Kyzyl-Art Pass, 39.406896° N, 73.345962° E, 4310 m, 21–22.VII.1992, O. Gorbunov leg. Alar expanse 24.0 mm. Sesiidae picture Nos 0003-0004–2013 (COGM); 9–10 — ♀, Kirgizstan, Transalai, env. of Kyzyl-Art Pass, 39.406896° N, 73.345962° E, 4310 m, 21–22.VII.1992, O. Gorbunov leg. Alar expanse 25.0 mm. Sesiidae picture Nos 0001-0002–2013 (COGM); 11–12 — B. kaabaki O. Gorbunov, 2001, holotype ♂, Tajikistan, E Pamir, Sarikol Mts., env. of Dunkeldyk lake, 17.VII.1997, A. Sotchivko leg. Alar expanse 25.5 mm. Sesiidae picture Nos 0313- 0314–2014 (COGM). 7, 9, 11 — dorsal view; 8, 10, 12 — ventral view. Рис 7–12. Bembecia spp. 7–10 — B. senilis (Grum-Grshimailo, 1890): 7–8 — ♂, КиргиЗстан, Трансалайский хребет, окрестности перевала КыЗыл-Арт, 39.406896° С, 73.345962° В, 4310 м, 21–22.VII.1992, О. Горбунов leg. РаЗмах крыльев 24.0 мм, Sesiidae снимки №№ 0003-0004–2023 (COGM); 9–10 — ♀, КиргиЗстан, Трансалайский хребет, окрестности перевала КыЗыл-Арт, 39.406896° С, 73.345962° В, 4310 м, 21–22.VII.1992, О. Горбунов leg. РаЗмах крыльев 25.0 мм, Sesiidae снимки №№ 0001-0002–2013 (COGM); 11– 12 — B. kaabaki O. Gorbunov, 2001, голотип ♂, Таджикистан, Восточный Памир, Сарыкольский хребет, окрестности оЗера Дункельдык, 17.VII.1997, А. Сочивко leg. РаЗмах крыльев 25.5 мм, Sesiidae снимки №№ 0313-0314–2014 (COGM). 7, 9, 11 — dorsal view; 8, 10, 12 — ventral view.

Figs 1–6. Bembecia sotchivkoi O in A new species of the genus Bembecia Hübner, 1819 ["1816"](Lepidoptera: Sesiidae) from the Gissar Mountain Range

Figs 1–6. Bembecia sotchivkoi O. Gorbunov, sp.n.: 1–2 — holotype ♂, alar expanse 25.1 mm. Sesiidae picture Nos 0355-0356–2013; 3–4 — paratype ♂, alar expanse 25.5 mm. Sesiidae picture Nos 0343-0344–2013; 5–6 — paratype ♀, alar expanse 24.9 mm, Sesiidae picture Nos 0353-0354–2013. 1, 3, 5 — dorsal view; 2, 4, 6 — ventral view. Рис. 1–6. Bembecia sotchivkoi O. Gorbunov, sp.n.: 1–2 — голотип ♂, раЗмах крыльев 25.1 мм. Sesiidae снимки №№ 0355-0356– 2013; 3–4 — паратип ♂, раЗмах крыльев 25.5 мм. Sesiidae снимки №№ 0343-0344–2013; 5–6 — паратип ♀, раЗмах крыльев 24.9 мм, Sesiidae снимки №№ 0353-0354–2013. 1, 3, 5 — вид сверху; 2, 4, 6 — вид сниЗу.

FIGURE 8 in Two new species of Diamesinae (Diptera: Chironomidae) from the Central Iranian Range and Elburz Mountains (Iran), with new faunistic records for the subfamily

FIGURE 8. Potthastia longimanus (Kieffer, 1922) adult male (A–B), Lake Huron, Bush Bay, MI, USA. A. hypopygium, arrows indicate phallapodeme. B. hypopygium, aedeagal lobe (AL), superior volsella (SVo), median volsella (MVo), and inferior volsella (IVo), white arrows indicate the boundary of aedeagal lobe and superior volsella. Scale bars are 50 µm.

FIGURE 9 in Two new species of Diamesinae (Diptera: Chironomidae) from the Central Iranian Range and Elburz Mountains (Iran), with new faunistic records for the subfamily

FIGURE 9. Bayesian Interface (BI) and Neighbor-Joining (NJ) trees of Sympotthastia Pagast, 1947 species, and one outgroup Lappodiamesa omelkoi Makarchenko et Makarchenko, 2013 inferred from the COI nucleotide sequence data (658 bp). Numbers on branches represent the posterior probabilities for BI and bootstrap value for NJ, respectively (values <0.95/95 omitted). The gray bars on the right are clusters estimated using three molecular species delimitation methods: ABGD, ASAP, and K2P.

FIGURE 4 in Two new species of Diamesinae (Diptera: Chironomidae) from the Central Iranian Range and Elburz Mountains (Iran), with new faunistic records for the subfamily

FIGURE 4. Diamesa kasymovi Kownacka et Kownacki, 1973 adult female (A-E). A. head. B. thorax. C. wing. D. genitalia, ventral. E. genitalia, dorsal. Scale bars are 100 µm.

FIGURE 6 in Two new species of Diamesinae (Diptera: Chironomidae) from the Central Iranian Range and Elburz Mountains (Iran), with new faunistic records for the subfamily

FIGURE 6. Sympotthastia golalae sp. nov. adult male. A. wing. B. hypopygium, aedeagal lobe, superior volsella, median volsella and phallapodeme indicated by arrows. C. superior volsella and spiniferous median volsella. Scale bars are 100 µm.

FIGURE 3 in Two new species of Diamesinae (Diptera: Chironomidae) from the Central Iranian Range and Elburz Mountains (Iran), with new faunistic records for the subfamily

FIGURE 3. Diamesa kasymovi Kownacka et Kownacki, 1973 adult male. A. antenna. B. hypopygium. C. hypopygium. Scale bars are 50 µm.

FIGURE 2 in Two new species of Diamesinae (Diptera: Chironomidae) from the Central Iranian Range and Elburz Mountains (Iran), with new faunistic records for the subfamily

FIGURE 2. Diamesa sahandensis sp. nov. adult male. A. antenna. B. head. C. thorax. D. wing. E. hypopygium, dorsal. F. hypopygium, ventral. G. superior volsella. H. gonostylus. I. gonostylus. Scale bars are 100 µm.

FIGURE 1 in Two new species of Diamesinae (Diptera: Chironomidae) from the Central Iranian Range and Elburz Mountains (Iran), with new faunistic records for the subfamily

FIGURE 1. Sampling habitats, East Azerbaijan Province (A–C), Kurdistan Province (D–G). A. sampling habitat in the stream near Sahand Mountain, Kandovan Village. B. stream channel passing through the Kandovan Village outskirts. C. stream near Kaleybar Village. D. stream on the outskirts of Bayanchub village. E. foreground of the stream on the outskirts of Bayanchub village F. sampling habitat in the tributary of Saqqez River. G. foreground of the tributary of Saqqez River.

FIGURE 5 in Two new species of Diamesinae (Diptera: Chironomidae) from the Central Iranian Range and Elburz Mountains (Iran), with new faunistic records for the subfamily

FIGURE 5. Sympotthastia golalae sp. nov. adult male (A–E). A. antenna. B. head. C. thorax. D. hypopygium. E. phallapodeme, aedeagal lobe, superior volsella, and median volsella. Scale bars are 100 µm.

FIGURE 7 in Two new species of Diamesinae (Diptera: Chironomidae) from the Central Iranian Range and Elburz Mountains (Iran), with new faunistic records for the subfamily

FIGURE 7. Sympotthastia golalae sp. nov. adult female (A–E). A. head. B. thorax. C. wing. D. genitalia, ventral. E. genitalia, dorsal. Scale bars are 100 µm.

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.

opennotspecifiedMar 2013View details →

Subspecies and Distribution. A. g. geoffroyi Kuhl, 1820 — S & SE Nicaragua (coastal region around San Juan del Norte or Martina Bay, probably ranging across the lowlands to the vicinity of Lake Managua and Lake Nicaragua on the Pacific coast); possibly in N Costa Rica. A. g. azuerensis Bole, 1937 — SC Panama, known only from the forested mountains of the W side of the Azuero Peninsula (Veraguas Province) in the vicinity of Ponuga, where it appears to be isolated; it may also occur to the W along the Pacific coastto the Burica Peninsula, near the Panamanian and Costa Rican border. A. g. frontatus Gray, 1842 — N & W Nicaragua and NW Costa Rica. A. g. grisescens Gray, 1866 — S Panama along the Pacific coast in the valley of the Rio Tuyra and SE through the Serrania del Sapo of extreme SE Panama into the Cordillera de Baudo of NW Colombia. A. g. ornatus Gray, 1871 — C & E Costa Rica, and Panama (from Chiriqui Province to the Serrania de San Blas E of the Canal Zone). A. g. vellerosus Gray, 1866 — E & SE Mexico (E San Luis Potosi, Veracruz, Tabasco, E Oaxaca, and Chiapas states), Guatemala (including the highlands), El Salvador, and Honduras (along the N coastto the lowlands of La Mosquitia in Gracias a Dios Department). A. g. yucatanensis Kellogg & Goldman, 1944 — SE Mexico (forests of the Yucatan Peninsula), NE Guatemala, and adjoining parts of Belize; intergrading in S Mexico (Campeche State) and Guatemala with vellerosus. in Atelidae

Subspecies and Distribution. A. g. geoffroyi Kuhl, 1820 — S & SE Nicaragua (coastal region around San Juan del Norte or Martina Bay, probably ranging across the lowlands to the vicinity of Lake Managua and Lake Nicaragua on the Pacific coast); possibly in N Costa Rica. A. g. azuerensis Bole, 1937 — SC Panama, known only from the forested mountains of the W side of the Azuero Peninsula (Veraguas Province) in the vicinity of Ponuga, where it appears to be isolated; it may also occur to the W along the Pacific coastto the Burica Peninsula, near the Panamanian and Costa Rican border. A. g. frontatus Gray, 1842 — N & W Nicaragua and NW Costa Rica. A. g. grisescens Gray, 1866 — S Panama along the Pacific coast in the valley of the Rio Tuyra and SE through the Serrania del Sapo of extreme SE Panama into the Cordillera de Baudo of NW Colombia. A. g. ornatus Gray, 1871 — C & E Costa Rica, and Panama (from Chiriqui Province to the Serrania de San Blas E of the Canal Zone). A. g. vellerosus Gray, 1866 — E & SE Mexico (E San Luis Potosi, Veracruz, Tabasco, E Oaxaca, and Chiapas states), Guatemala (including the highlands), El Salvador, and Honduras (along the N coastto the lowlands of La Mosquitia in Gracias a Dios Department). A. g. yucatanensis Kellogg & Goldman, 1944 — SE Mexico (forests of the Yucatan Peninsula), NE Guatemala, and adjoining parts of Belize; intergrading in S Mexico (Campeche State) and Guatemala with vellerosus.

opennotspecifiedJan 2009View details →

Distribution. Arid mountainous regions of the Middle East. Known populations in Egypt, Israel, Jordan, Oman, Saudi Arabia, and United Arab Emirates. The species also ranges across much of Afghanistan and Iran, and surrounding regions in Pakistan, Tajikistan, Turkmenistan, and Uzbekistan. in Canidae

Distribution. Arid mountainous regions of the Middle East. Known populations in Egypt, Israel, Jordan, Oman, Saudi Arabia, and United Arab Emirates. The species also ranges across much of Afghanistan and Iran, and surrounding regions in Pakistan, Tajikistan, Turkmenistan, and Uzbekistan.

opennotspecifiedOct 2019View details →

Distribution. Philippines (Mountain and Benguet provinces on Luzon I, and Surigao del Norte and Davao del Sur provinces on Mindanao I), Borneo (Crocker Range in Sabah, and Kubah National Park in Sarawak), NE & C Sulawesi, and Moluccas (Buru and Ambon Is). A record from Mt Isarog (Camarines Sur Province on Luzon I) is assigned to the Pipustrellusjavanicus complex. in Vespertilionidae

Distribution. Philippines (Mountain and Benguet provinces on Luzon I, and Surigao del Norte and Davao del Sur provinces on Mindanao I), Borneo (Crocker Range in Sabah, and Kubah National Park in Sarawak), NE & C Sulawesi, and Moluccas (Buru and Ambon Is). A record from Mt Isarog (Camarines Sur Province on Luzon I) is assigned to the Pipustrellusjavanicus complex.