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FIGURE 6 in Freshwater and brackish water fishes of Sakhalin Island (Russia) in inland and coastal waters: an annotated checklist with taxonomic comments
FIGURE 6. Map of Sakhalin Island with indication of natural entities (islands, rivers, lakes, gulfs, etc.).
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. U. a. americanus Pallas, 1780 — Alaska to E Canada and E USA. U. a. altifrontalis Elliot, 1903 — Pacific coast USA and Canada (S British Columbia). U. a. amblyceps Baird, 1859 — SW USA. U. a. californiensisJ. Miller, 1900 — SW USA (interior California). U. a. carlottae Osgood, 1901 — W Canada (Queen Charlotte Is). U. a. cinnamomum Audubon & Bachman, 1854 — Rocky Mts of Canada and USA. U. a. emmonsu Dall, 1895 — SE Alaska. U. a. eremicus Merriam, 1904 — E Mexico. U. a. floridanus Merriam, 1896 — SE USA (Florida). U. a. hamilton: Cameron, 1957 — E Canada (Newfoundland). U. a. kermodei Hornaday, 1905 — W Canada (coastal British Columbia). U. a. luteolus Griffith, 1821 — S USA (Louisiana). U. a. machetes Elliot, 1903 — W Mexico. U. a. pernigerJ. A. Allen, 1910 — Alaska (Kenai Peninsula). U. a. pugnax Swarth, 1911 — islands of SE Alaska. U. a. vancouver: Hall, 1928 — SW Canada (Vancouver I). in Ursidae
Subspecies and Distribution. U. a. americanus Pallas, 1780 — Alaska to E Canada and E USA. U. a. altifrontalis Elliot, 1903 — Pacific coast USA and Canada (S British Columbia). U. a. amblyceps Baird, 1859 — SW USA. U. a. californiensisJ. Miller, 1900 — SW USA (interior California). U. a. carlottae Osgood, 1901 — W Canada (Queen Charlotte Is). U. a. cinnamomum Audubon & Bachman, 1854 — Rocky Mts of Canada and USA. U. a. emmonsu Dall, 1895 — SE Alaska. U. a. eremicus Merriam, 1904 — E Mexico. U. a. floridanus Merriam, 1896 — SE USA (Florida). U. a. hamilton: Cameron, 1957 — E Canada (Newfoundland). U. a. kermodei Hornaday, 1905 — W Canada (coastal British Columbia). U. a. luteolus Griffith, 1821 — S USA (Louisiana). U. a. machetes Elliot, 1903 — W Mexico. U. a. pernigerJ. A. Allen, 1910 — Alaska (Kenai Peninsula). U. a. pugnax Swarth, 1911 — islands of SE Alaska. U. a. vancouver: Hall, 1928 — SW Canada (Vancouver I).
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. Endemic to Chile, with a disjunct distribution in the forests of Chiloé Island, and on the mainland coastal mountains in Nahuelbuta National Park. Evidence of a new population was foud recently at Punta Chan Chan, N of Valdivia. in Canidae
Distribution. Endemic to Chile, with a disjunct distribution in the forests of Chiloé Island, and on the mainland coastal mountains in Nahuelbuta National Park. Evidence of a new population was foud recently at Punta Chan Chan, N of Valdivia.
Distribution. Coastal NW Mexico, including areas in Sebastian Vizcaino Bay and Tortuga Bay on Pacific coast, Gulf of California from C Baja California (Islas Esmeraldas) to Bay of Paz and Punta Coyotes in Baja California Sur, and from Bay of San Jorge S to Guaymas in Sonora; also on many islands. in Vespertilionidae
Distribution. Coastal NW Mexico, including areas in Sebastian Vizcaino Bay and Tortuga Bay on Pacific coast, Gulf of California from C Baja California (Islas Esmeraldas) to Bay of Paz and Punta Coyotes in Baja California Sur, and from Bay of San Jorge S to Guaymas in Sonora; also on many islands.
FIGURE 10. Cognateosymtes serraticoxae Labay, 2018 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994
FIGURE 10. Cognateosymtes serraticoxae Labay, 2018, coastal shallow waters off southeastern Sakhalin Island, female, 6.5 mm: a—incisor and molar of left mandible, b—incisor and raker setae of right mandible, c—maxilliped, d—maxilla 1, e—maxilla 2, f—gnathopod 1, g—gnathopod 2; scales: a, b, d, e—0.1 mm, c, f, g—0.5 mm
FIGURE 9 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994
FIGURE 9. Eosymtes magnumoculis sp. nov., paratype, female, 4.8 mm (the shelf of eastern Sakhalin): a—gnathopod 1, b— palm of propodus and dactylus of gnathopod 1, c—gnathopod 2, d—palm of propodus and dactylus of gnathopod 1; paratype, female, 5.2 mm (the shelf of eastern Sakhalin): e—coxal plate 2 with coxal gill and brood plate; paratype, female, 6.3 mm (the shelf of western Kamchatka): f, g—inner side of coxal plate 1; scales: a, c, e—0.5 mm, b, d, f—0.1 mm; g—0.02 mm
FIGURE 6 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994
FIGURE 6. Eosymtes magnumoculis sp. nov., holotype, female: a—gnathopod 2, b—palm of propodus and dactylus of gnathopod 2, c—pereopod 3; d—pereopod 4; scales: a, c, d—1 mm, b—0.1 mm
FIGURE 7 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994
FIGURE 7. Eosymtes magnumoculis sp. nov., holotype, female: a—pereopod 5, b—pereopod 6, c—pereopod 7, d, e, f—epimeral plates 1–3, g—pleopod 2, h—coupling spines of pleopod 3, i, j, k—coupling setae of pleopods 1, 2 and 3; scales: a–g—1 mm, h–k—0.1 mm
FIGURE 8 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994
FIGURE 8. Eosymtes magnumoculis sp. nov., holotype, female: a—uropod 1, b—uropod 2, c—uropod 3, d—telson; paratype, female, 6.3 mm (the shelf of western Kamchatka): e—microstructure of surface; scales: a, b, c—1 mm, d—0.2 mm, e—0.01 mm
FIGURE 5 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994
FIGURE 5. Eosymtes magnumoculis sp. nov., holotype, female: a—maxilla 1, b—maxilla 2, c—maxilliped, d—gnathopod 1, e—palm of propodus and dactylus of gnathopod 1; paratype, female, 5.3 mm: f—lower lips; paratype, female, 6.3 mm: g—incisor and molar of right mandible; scales: d—0.5 mm; c—0.2 mm; a, b, e, f—0.1 mm
FIGURE 4 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994
FIGURE 4. Eosymtes magnumoculis sp. nov., holotype, female, 8.9 mm (the shelf of eastern Sakhalin): a—lateral view, b—cephalon, c—upper lip, d—left mandible, e—incisor and molar of left mandible, f—incisor and molar of right mandible; paratype, female, 6.5 mm (the shelf of eastern Sakhalin): g—antenna 1, h—additional flagellum of antenna 1, i—antenna 2, j—incisor and molar of right mandible, k—lacinia mobilis of right mandible; paratype, female, 5.3 mm (the shelf of eastern Sakhalin): l—lacinia mobilis of right mandible; paratype, female, 6.3 mm (the shelf of western Kamchatka): m—lacinia mobilis of right mandible: scales: a, g, i—1 mm; b—0.5 mm; c, d—0.2 mm, e, f, h, j, k, l, m—0.1 mm
FIGURE 2 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994
FIGURE 2. Eosymtinae Bousfield & Hendrycks, 1994: a–c—peduncle of antenna 1; d–f—maxilla 2; g–i—palp of maxilliped; j–l—coxal plates 1–3 posteroventrally; m, n, o—propodus and dactylus of pereopods 3–7; a, d, g, j, m—Eosymtes minutus Bousfield and Hendrycks, 1994 (from Bousfield and Hendrycks 1994), b, e, h, k, n—Eosymtes magnumoculis sp. nov., c, f, i, l, o—Cognateosymtes serraticoxae Labay, 2018 (from Labay 2018)
FIGURE 3 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994
FIGURE 3. Eosymtinae Bousfield & Hendrycks, 1994: a—urosome segments 1–3; c, f—uropod 1; d, g—uropod 2; b, e, h—uropod 3; a, b—Eosymtes minutus Bousfield and Hendrycks, 1994 (modified from Bousfield and Hendrycks 1994), c, d, e—Eosymtes magnumoculis sp. nov., f, g, h—Cognateosymtes serraticoxae Labay, 2018 (from Labay 2018)
FIGURE 1 in Review of amphipods of the family Pleustidae Buchholz, 1874 (Amphipoda) from the coastal waters of Sakhalin Island (Far East of Russia). II. Subfamily Eosymtinae Bousfield & Hendrycks, 1994
FIGURE 1. Eosymtinae Bousfield & Hendrycks, 1994, lateral view: a—Eosymtes minutus Bousfield and Hendrycks, 1994 (from Bousfield and Hendrycks 1994: fig. 7), b—Eosymtes magnumoculis sp. nov., c—Cognateosymtes serraticoxae Labay, 2018 (from Labay 2018: fig. 2a)
Subspecies and Distribution. A.j.jamaicensisLeach,1821—GreaterAntilles(Jamaica,Hispaniola,PuertoRico,andVieques,includingGonaveandMonaIs),LesserAntilles,Aruba(NetherlandAntilles),andProvidenciaandSanAndrésIs. A.j.parvipesRehn,1902—Cuba,includingIsladelaJuventud,SBahamas(GreatInaguaandMayaguanaIs),andCaymanIs(GrandCayman,LittleCayman,andCaymanBrac). A.j.paulusW.B.Davis,1970—CentralAmericafromSEMexico(Chiapas)SEtoNWCostaRica(GuanacasteProvince). A.j.richardsoniJ.A.Allen,1908—fromSEMexico(NChiapas)SEthroughCentralAmerica,alongAtlanticcoastandalongbothversantsfromthevicinityofPuntaArenasinNWCostaRica,intoNWColombia. A.j.triomylusHandley,1966—PacificslopeofMexicofromSinaloatoOaxaca. A. j. yucatanicus]. A. Allen, 1904 — Gulf coastal plains and offshore islands from Tamaulipas, Mexico, SE to Yucatan Peninsula (including CozumelI), Belize, and Bay Is off Honduras. in Phyllostomidae
Subspecies and Distribution. A.j.jamaicensisLeach,1821—GreaterAntilles(Jamaica,Hispaniola,PuertoRico,andVieques,includingGonaveandMonaIs),LesserAntilles,Aruba(NetherlandAntilles),andProvidenciaandSanAndrésIs. A.j.parvipesRehn,1902—Cuba,includingIsladelaJuventud,SBahamas(GreatInaguaandMayaguanaIs),andCaymanIs(GrandCayman,LittleCayman,andCaymanBrac). A.j.paulusW.B.Davis,1970—CentralAmericafromSEMexico(Chiapas)SEtoNWCostaRica(GuanacasteProvince). A.j.richardsoniJ.A.Allen,1908—fromSEMexico(NChiapas)SEthroughCentralAmerica,alongAtlanticcoastandalongbothversantsfromthevicinityofPuntaArenasinNWCostaRica,intoNWColombia. A.j.triomylusHandley,1966—PacificslopeofMexicofromSinaloatoOaxaca. A. j. yucatanicus]. A. Allen, 1904 — Gulf coastal plains and offshore islands from Tamaulipas, Mexico, SE to Yucatan Peninsula (including CozumelI), Belize, and Bay Is off Honduras.
Distribution. NE USA,in coastal S Maine, coastal and Merrimack River valley region of S New Hampshire, SE New York, W Massachusetts (including parts of Cape Cod), W & E (E of the Connecticut River) Connecticut, and Rhode Island. in Leporidae
Distribution. NE USA,in coastal S Maine, coastal and Merrimack River valley region of S New Hampshire, SE New York, W Massachusetts (including parts of Cape Cod), W & E (E of the Connecticut River) Connecticut, and Rhode Island.
Distribution. NW Madagascar from the Mahavavy River S to the Andranomalaza River, the E limit is poorly defined, butlikely occurs at the Tsaratanana Massif, and there are additional populations in forests of the Ampasindava Peninsula, on the inshore islands of Nosy Be and Nosy Komba, and in the coastal forests NE of Ambanja (including the peninsula leading to Nosy Faly). Introduced into the small islet of Nosy Tanikely. in Lemuridae
Distribution. NW Madagascar from the Mahavavy River S to the Andranomalaza River, the E limit is poorly defined, butlikely occurs at the Tsaratanana Massif, and there are additional populations in forests of the Ampasindava Peninsula, on the inshore islands of Nosy Be and Nosy Komba, and in the coastal forests NE of Ambanja (including the peninsula leading to Nosy Faly). Introduced into the small islet of Nosy Tanikely.
Subspecies and Distribution. P.a.alectoTemminck,1837—Sulawesi,includingSelayarI. P.a.aterrimusMatschie,1899—EJava,Bawean,andLombokIs.Theserecordshavenotbeenconfirmedrecently. P. a. gouldii Peters, 1868 — N & E Australia (including several islands on the N & E coasts: Tiwi, Groote Eylandt, Torres Strait, Magnetic, Carlisle, Percy, North Keppel, and Fraser) and coastal plain of S New Guinea (Western and Central provinces in P.a. New Guinea); in P.a. New Guinea it might also occur in Gulf Province and offshore islands off S coast E to Yule I. P a. morio K. Andersen, 1908 — Lesser Sundas (Sumba and Savu Is). in Pteropodidae
Subspecies and Distribution. P.a.alectoTemminck,1837—Sulawesi,includingSelayarI. P.a.aterrimusMatschie,1899—EJava,Bawean,andLombokIs.Theserecordshavenotbeenconfirmedrecently. P. a. gouldii Peters, 1868 — N & E Australia (including several islands on the N & E coasts: Tiwi, Groote Eylandt, Torres Strait, Magnetic, Carlisle, Percy, North Keppel, and Fraser) and coastal plain of S New Guinea (Western and Central provinces in P.a. New Guinea); in P.a. New Guinea it might also occur in Gulf Province and offshore islands off S coast E to Yule I. P a. morio K. Andersen, 1908 — Lesser Sundas (Sumba and Savu Is).
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.