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36 results for “Kyushu Island”
FIGURE 6 in A new species of Pseudodiaptomus (Copepoda: Calanoida) from Japan, with notes on the closely related P. inopinus Burckhardt, 1913 from Kyushu Island
FIGURE 6. Pseudodiaptomus nansei sp. nov. Male (A–F, allotype; G, specimen from Ura-gawa River): A, habitus, dorsal; B, habitus, right lateral; C, second urosomite, ventral; D, right antennule; E, leg 5, posterior; F, leg 5, anterior; G, moderately paddle-shaped second exopodal segment of left leg 5.
Distribution. Bhutan, China, India, Japan (Hokkaido), North and South Korea, Nepal, Laos, Mongolia, N Myanmar, Russia, Taiwan, and N Thailand. Introduced to several Japanese islands (Honshu, Kyushu & Shikoku Is). in Mustelidae
Distribution. Bhutan, China, India, Japan (Hokkaido), North and South Korea, Nepal, Laos, Mongolia, N Myanmar, Russia, Taiwan, and N Thailand. Introduced to several Japanese islands (Honshu, Kyushu & Shikoku Is).
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.
Distribution. Originally endemic to Japan, and mainly distributed in Honshu, Shikoku, and Kyushu; it has been found in other small islands including Sado, Oki Is, Mishima, Okinoshima (Fukuoka Prefecture), Tanegashima, Yakushima, Nakanoshima (Tokara Is), and Izu Is. Introduced to Hokkaido and Jeju I (South Korea). in Soricidae
Distribution. Originally endemic to Japan, and mainly distributed in Honshu, Shikoku, and Kyushu; it has been found in other small islands including Sado, Oki Is, Mishima, Okinoshima (Fukuoka Prefecture), Tanegashima, Yakushima, Nakanoshima (Tokara Is), and Izu Is. Introduced to Hokkaido and Jeju I (South Korea).
Distribution. Originally distributed throughout the Indo-Malayan Region and S China, including Taiwan, Hainan, and Sri Lanka (only original range shaded in the map). Possible human-mediate introduced range in Maldives, islands of Malaysia, Indonesia, Brunei, Philippines, Japan (Kyushu and Ryukyu Is), Guam, Palau, and New Guinea. Introduced in historical times into East Africa (Egypt, Sudan, Eritrea, Djibouti, Kenya, Rwanda, and Tanzania), Pemba and Zanzibar (Unguja) Is, Madagascar, Comoro Is, Mauritius, Réunion I, and into coastal Arabia (in the vicinity of seaports in Iraq, Kuwait, Bahrain, Saudi Arabia, Yemen, and Oman). in Soricidae
Distribution. Originally distributed throughout the Indo-Malayan Region and S China, including Taiwan, Hainan, and Sri Lanka (only original range shaded in the map). Possible human-mediate introduced range in Maldives, islands of Malaysia, Indonesia, Brunei, Philippines, Japan (Kyushu and Ryukyu Is), Guam, Palau, and New Guinea. Introduced in historical times into East Africa (Egypt, Sudan, Eritrea, Djibouti, Kenya, Rwanda, and Tanzania), Pemba and Zanzibar (Unguja) Is, Madagascar, Comoro Is, Mauritius, Réunion I, and into coastal Arabia (in the vicinity of seaports in Iraq, Kuwait, Bahrain, Saudi Arabia, Yemen, and Oman).
Distribution. Japan, including Hokkaido, Honshu, Shikoku, Kyushu, and adjacent islands of Kinkasan, Awashima, Sado, Oki Is (Dogo and Nishino), Awaji, Shodo, Miyajima, Tsushima, Gotd Is (Fukuejima and Nakadorijima), Amakusa-shimoshima, and OsumiIs (Yakushima and Tanegashima). in Muridae
Distribution. Japan, including Hokkaido, Honshu, Shikoku, Kyushu, and adjacent islands of Kinkasan, Awashima, Sado, Oki Is (Dogo and Nishino), Awaji, Shodo, Miyajima, Tsushima, Gotd Is (Fukuejima and Nakadorijima), Amakusa-shimoshima, and OsumiIs (Yakushima and Tanegashima).
Fig. 4. Neocaridina ikiensis n in A New Species of Land-locked Freshwater Shrimp of the Genus Neocaridina (Decapoda: Caridea: Atyidae) from Iki Island, Kyushu, Japan
Fig. 4. Neocaridina ikiensis n. sp. (A) Cephalothorax and cephalic appendages, lateral view; (B) 1st pereiopod; (C) 2nd pereiopod; (D) 3rd pereiopod; (E) the same, dactylus; (F) 5th pereiopod; (G) the same, dactylus. Scale bars: A = 2 mm; B-D, F = 0.3 mm; E, G = 0.15 mm (female, cl 5.1 mm, paratype, ZRC 2017.0961).
Fig. 6 in A New Species of Land-locked Freshwater Shrimp of the Genus Neocaridina (Decapoda: Caridea: Atyidae) from Iki Island, Kyushu, Japan
Fig. 6. Bayesian inference (BI) tree of Neocaridina spp. from East Asia and outgroups based COI gene. Probability values at the nodes represent bootstrap values for BI and maximum likelihood (ML). For abbreviations of haplotypes see table 1.
Fig. 3. Neocaridina ikiensis n in A New Species of Land-locked Freshwater Shrimp of the Genus Neocaridina (Decapoda: Caridea: Atyidae) from Iki Island, Kyushu, Japan
Fig. 3. Neocaridina ikiensis n. sp. (A) 1st pereiopod; (B) 2nd pereiopod; (C) 3rd pereiopod; (D) the same, dactylus; (E) 5th pereiopod; (F) the same, dactylus; (G, H) male 1st pleopod; (I, J) male 2nd pleopod; (K) uropodal diaeresis. Scale bars: A, B, C, E, G, I = 0.3 mm; D, F, H, J, K = 0.15 mm (male, cl 4.6 mm, paratype, ZRC 2017.0960).
Fig. 2. Neocaridina ikiensis n in A New Species of Land-locked Freshwater Shrimp of the Genus Neocaridina (Decapoda: Caridea: Atyidae) from Iki Island, Kyushu, Japan
Fig. 2. Neocaridina ikiensis n. sp. (A) Cephalothorax and cephalic appendages, lateral view; (B) telson; (C) distal portion of telson; (D) preanal carina; (E) scaphocerite; (F) mandible; (G) maxillula; (H) maxilla; (I) 1st maxilliped; (J) 2nd maxilliped; (K) 3rd maxilliped. Scale bars: A-C = 2 mm; F-K = 0.3 mm; D = 1.5 mm; E = 4 mm (male, cl 4.6 mm, paratype, ZRC 2017.0960).
FIGURE 7 in A new species of the genus Urumaelmis Satô (Coleoptera, Elmidae, Macronychini) from Kyushu Island, Japan
FIGURE 7. Type locality of Urumaelmis flammea sp. nov.
FIGURE 1 in Fossil decapods from the Upper Quaternary in Shinjima Island in Kagoshima Kyushu, Japan, and description of a new species of ghost shrimp (Axiidea Eucalliacidae)
FIGURE 1. Map showing the fossil localities.
Linked collectors and determiners for: A new species of the genus Urumaelmis Satô (Coleoptera, Elmidae, Macronychini) from Kyushu Island, Japan.
Natural history specimen data linked to collectors and determiners held within, "A new species of the genus Urumaelmis Satô (Coleoptera, Elmidae, Macronychini) from Kyushu Island, Japan". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/a69af48a-a7ad-4345-b181-8d2d476a3631">https://bionomia.net/dataset/a69af48a-a7ad-4345-b181-8d2d476a3631</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/a69af48a-a7ad-4345-b181-8d2d476a3631">https://gbif.org/dataset/a69af48a-a7ad-4345-b181-8d2d476a3631</a>. Formatted as a Frictionless Data package.
Fig. 5 in A New Species of Land-locked Freshwater Shrimp of the Genus Neocaridina (Decapoda: Caridea: Atyidae) from Iki Island, Kyushu, Japan
Fig. 5. Live coloration of Neocaridina ikiensis n. sp. (A) and its habitat in Iki Island (B).
Distribution. NE & EC China (Heilongjiang, Jilin, Henan, Anhui, and Zhejiang), Korean Peninsula, and numerous islands in Japan (Hokkaido, Honshu, Shikoku, Kyushu, Tsushima, Iki, Fukue, and Okinawajima); there are also visual and echolocation records from the Russian Far East, but further investigation is needed. in Vespertilionidae
Distribution. NE & EC China (Heilongjiang, Jilin, Henan, Anhui, and Zhejiang), Korean Peninsula, and numerous islands in Japan (Hokkaido, Honshu, Shikoku, Kyushu, Tsushima, Iki, Fukue, and Okinawajima); there are also visual and echolocation records from the Russian Far East, but further investigation is needed.
Fig. 1 in A New Species of Land-locked Freshwater Shrimp of the Genus Neocaridina (Decapoda: Caridea: Atyidae) from Iki Island, Kyushu, Japan
Fig. 1. Collection sites (marked in red circles) for Neocaridina ikiensis n. sp. in Iki Island.
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