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FIGURE 3 in First records of interstitial leptocytherids (Crustacea, Ostracoda): two new species and a redescription of Callistocythere ventricostata Ruan & Hao, 1988 collected from the Okinawa Islands, southern Japan

FIGURE 3. Carapace of Callistocythere intermedia sp. nov. (SEM images). A, B, external lateral view of male right and left valves, respectively (holotype, SUM-CO-2342); C, D, external lateral view of female right and left valves, respectively (paratype, SUM-CO-2347); E, F, internal lateral view of male left and right valves, respectively (paratype, SUM-CO-2342); G, H, internal lateral view of female left and right valves, respectively (paratype, SUM-CO-2348); I, complete female carapace in ventral view (paratype, SUM-CO-2349); J, complete male carapace in dorsal view (paratype, SUM-CO-2344); K, L, posterior and anterior socket of hingement on female left valve, respectively (paratype, SUM-CO-2348); M, N, posterior and anterior teeth of hingement on female right valve, respectively (paratype, SUM-CO-2348). Scale: 50 µm (A–J) and 10 µm (K–N).

FIGURE 2 in First records of interstitial leptocytherids (Crustacea, Ostracoda): two new species and a redescription of Callistocythere ventricostata Ruan & Hao, 1988 collected from the Okinawa Islands, southern Japan

FIGURE 2. Callistocythere intermedia sp. nov. Internal view of male carapace. A, left valve; B, right valve (holotype, SUM-CO- 2342). Scale: 50 µm.

FIGURE 1 in First records of interstitial leptocytherids (Crustacea, Ostracoda): two new species and a redescription of Callistocythere ventricostata Ruan & Hao, 1988 collected from the Okinawa Islands, southern Japan

FIGURE 1. Maps showing the location of the study area. A, map of Japan; B, map of the Okinawa Islands; C, sampling site of this study (Sesoko Beach).

FIGURE 2. Eutrichopagurus shirakawai n. gen., n in A new genus and new species of Paguridae (Crustacea: Decapoda: Anomura) from shallow subtidal waters in Okinawa Island, the Ryukyu Islands, Japan

FIGURE 2. Eutrichopagurus shirakawai n. gen., n. sp., holotype, female (sl 1.85 mm), CBM-ZC 12569, right cheliped. A, entire right cheliped, mesial view; B, same, lateral view; C, chela, dorsal view; D, carpus, dorsal view. Microscopic granules on surfaces omitted. Scale bar: 1 mm.

FIGURE 1. Eutrichopagurus shirakawai n. gen., n in A new genus and new species of Paguridae (Crustacea: Decapoda: Anomura) from shallow subtidal waters in Okinawa Island, the Ryukyu Islands, Japan

FIGURE 1. Eutrichopagurus shirakawai n. gen., n. sp., holotype, female (sl 1.85 mm), CBM-ZC 12569. A, arthrobranch on left fourth pereopod; B, shield and cephalic appendages, dorsal view; C, carapace, dorsal view; D, ultimate peduncular segment and flagella of left antennule, lateral view; E, proximal half of left antennal flagellum, dorsal view; F, left third maxilliped, lateral view; G, same, basis and ischium, ventral view; H, coxae of third pereopods and thoracic sixth sternite, ventral view; I, left fourth pereopod, lateral view; J, telson, dorsal view. Scale bars: 0.25 mm for A; 0.5 mm for B, D–J; 1 mm for C. setae

FIGURE 4. Eutrichopagurus shirakawai n. gen., n in A new genus and new species of Paguridae (Crustacea: Decapoda: Anomura) from shallow subtidal waters in Okinawa Island, the Ryukyu Islands, Japan

FIGURE 4. Eutrichopagurus shirakawai n. gen., n. sp., holotype, female (sl 1.85 mm), CBM-ZC 12569, ambulatory legs. A, right second pereopod, lateral view; B, same, dactylus, mesial view (microscopic granules on surface omitted); C, left third pereopod, lateral view; D, same, dactylus, lateral view (microscopic granules on surface omitted). Scale bars: 0.5 mm.

FIGURE 3. Eutrichopagurus shirakawai n. gen., n in A new genus and new species of Paguridae (Crustacea: Decapoda: Anomura) from shallow subtidal waters in Okinawa Island, the Ryukyu Islands, Japan

FIGURE 3. Eutrichopagurus shirakawai n. gen., n. sp., holotype, female (sl 1.85 mm), CBM-ZC 12569, left cheliped. A, entire left cheliped, mesial view; B, same, lateral view; C, chela and carpus, dorsal view. Microscopic granules on surfaces omitted. Scale bar: 1 mm.

FIGURE 5. Eutrichopagurus shirakawai n. gen., n in A new genus and new species of Paguridae (Crustacea: Decapoda: Anomura) from shallow subtidal waters in Okinawa Island, the Ryukyu Islands, Japan

FIGURE 5. Eutrichopagurus shirakawai n. gen., n. sp., holotype, female (sl 1.85 mm), CBM-ZC 12569. A, entire animal in dorsal view; B, living animal in anterior view, in situ (photo taken by N. Shirakawa).

FIGURE 5. Munida zebra Macpherson, 1994 in New records of the squat lobster genus Munida Leach, 1820 (Crustacea: Decapoda: Anomura: Munididae) from deep-water off Okinawa Islands, Ryukyu Islands, Japan, with description of a new species

FIGURE 5. Munida zebra Macpherson, 1994, female (cl 17.5 mm), CBM-ZC 11349, habitus in dorsal view, showing colouration in life.

FIGURE 4. Munida zebra Macpherson, 1994 in New records of the squat lobster genus Munida Leach, 1820 (Crustacea: Decapoda: Anomura: Munididae) from deep-water off Okinawa Islands, Ryukyu Islands, Japan, with description of a new species

FIGURE 4. Munida zebra Macpherson, 1994, female (cl 17.5 mm), CBM-ZC 11349. A, left cheliped, merus and carpus, ventral view (setae omitted); B, same, chela, ventral view; C, left second pereopod, lateral view; D, same, dactylus and distal part of propodus, lateral view; E, left third pereopod, lateral view (setae omitted); F, left fourth pereopod, lateral view (setae omitted). Scale bars: A–C, E, F = 5 mm; D = 2 mm.

FIGURE 2. Munida pollioculus n in New records of the squat lobster genus Munida Leach, 1820 (Crustacea: Decapoda: Anomura: Munididae) from deep-water off Okinawa Islands, Ryukyu Islands, Japan, with description of a new species

FIGURE 2. Munida pollioculus n. sp., holotype, female (cl 16.9 mm), CBM-ZC 11348. A, left third maxilliped, lateral view (setae omitted); right cheliped, merus, ventral view (setae omitted); B, cheliped ischium and merus, ventral view (setae omitted); C, same, carpus and chela, ventral view; D, right second pereopod, lateral view; E, same, dactylus and distal part of propodus, lateral view; F, right third pereopod, lateral view (setae omitted); G, right fourth pereopod, lateral view (setae omitted). Scale bars: B–D, F, G = 5 mm; A = 2 mm; E = 1 mm.

FIGURE 3. Munida zebra Macpherson, 1994 in New records of the squat lobster genus Munida Leach, 1820 (Crustacea: Decapoda: Anomura: Munididae) from deep-water off Okinawa Islands, Ryukyu Islands, Japan, with description of a new species

FIGURE 3. Munida zebra Macpherson, 1994, female (cl 17.5 mm), CBM-ZC 11349. A, carapace, pleon and cephalic appendages, dorsal view (setae on carapace ridges and striae omitted; distal 2 articles of antennular peduncles omitted); B, thoracic sternite, ventral view; C, pleomere 6, telson and right uropod, outer view (setae on striae on pleomere 6 shown); D, basal article of left antennular peduncle, antennal peduncle and anterior part of pterygostomial flap, ventral view; E, left third maxilliped, lateral view (setae omitted); F, left cheliped, merus, dorsal view (setae omitted); G, same, carpus and chela, ventral view (setae omitted). Scale bars: A, F, G = 5 mm; C–E = 2 mm.

FIGURE 1. Munida pollioculus n in New records of the squat lobster genus Munida Leach, 1820 (Crustacea: Decapoda: Anomura: Munididae) from deep-water off Okinawa Islands, Ryukyu Islands, Japan, with description of a new species

FIGURE 1. Munida pollioculus n. sp., holotype, female (cl 16.9 mm), CBM-ZC 11348. A, carapace, pleon and cephalic appendages, dorsal view (setae on carapace ridges and striae omitted; distal 2 articles of antennular peduncles omitted); B, thoracic sternum, ventral view; C, pleomere 6, outer view; D, telson and right uropod, outer view (setae omitted); E, basal article of left antennular peduncle, antennal peduncle and anterior part of pterygostomial flap, ventral view; F, right cheliped, dorsal view (setae omitted). Scale bars: A, F = 5 mm; B–E = 2 mm.

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.

opennotspecifiedJul 2018View details →

Distribution. Endemic to the Ryukyu Is, including 15 small islands of both the Amami and Okinawa Is; it may be distributed to the other small islands as well. in Soricidae

Distribution. Endemic to the Ryukyu Is, including 15 small islands of both the Amami and Okinawa Is; it may be distributed to the other small islands as well.

opennotspecifiedNov 2017View details →

On following pages: 507. Cansdale's Swamp Rat (Malacomys cansdalel); 508. Edwards's Swamp Rat (Malacomys edwards); 509. Alpine Field Mouse (Apodemus alpicola), 510. Long-tailed Field Mouse (Apodemus sylvaticus); 511. Striped Field Mouse (Apodemus agrarius); 512. Western Broad-toothed Field Mouse (Apodemus epimelas); 513. Hyrcanian Field Mouse (Apodemus hyrcanicus); 514. Caucasus Field Mouse (Apodemus ponticus); 515. Herb Field Mouse (Apodemus uralensis); 516. Yellow-necked Field Mouse (Apodemus flavicollis); 517. Eastern Broad-toothed Field Mouse (Apodemus mystacinus), 518. Steppe Field Mouse (Apodemus witherbyi); 519. Nepalese Field Mouse (Apodemus gurkha); 520. Himalayan Field Mouse (Apodemus pallipes); 521. Kashmir Field Mouse (Apodemus rusiges); 522. Chevrier's Field Mouse (Apodemus chevrieri); 523. South China Field Mouse (Apodemus draco); 524. Large-eared Field Mouse (Apodemus latronum); 525. Taiwan Field Mouse (Apodemus semotus); 526. Korean Field Mouse (Apodemus peninsulae); 527. Small Japanese Field Mouse (Apodemus argenteus); 528. Large Japanese Field Mouse (Apodemus speciosus); 529. Okinawa Island Spiny Rat (Tokudaia muenninki); 530. Amami Spiny Rat (Tokudaiaosimensis); 531. Tokunoshima Spiny Rat (Tokudaia tokunoshimensis). in Muridae

On following pages: 507. Cansdale's Swamp Rat (Malacomys cansdalel); 508. Edwards's Swamp Rat (Malacomys edwards); 509. Alpine Field Mouse (Apodemus alpicola), 510. Long-tailed Field Mouse (Apodemus sylvaticus); 511. Striped Field Mouse (Apodemus agrarius); 512. Western Broad-toothed Field Mouse (Apodemus epimelas); 513. Hyrcanian Field Mouse (Apodemus hyrcanicus); 514. Caucasus Field Mouse (Apodemus ponticus); 515. Herb Field Mouse (Apodemus uralensis); 516. Yellow-necked Field Mouse (Apodemus flavicollis); 517. Eastern Broad-toothed Field Mouse (Apodemus mystacinus), 518. Steppe Field Mouse (Apodemus witherbyi); 519. Nepalese Field Mouse (Apodemus gurkha); 520. Himalayan Field Mouse (Apodemus pallipes); 521. Kashmir Field Mouse (Apodemus rusiges); 522. Chevrier's Field Mouse (Apodemus chevrieri); 523. South China Field Mouse (Apodemus draco); 524. Large-eared Field Mouse (Apodemus latronum); 525. Taiwan Field Mouse (Apodemus semotus); 526. Korean Field Mouse (Apodemus peninsulae); 527. Small Japanese Field Mouse (Apodemus argenteus); 528. Large Japanese Field Mouse (Apodemus speciosus); 529. Okinawa Island Spiny Rat (Tokudaia muenninki); 530. Amami Spiny Rat (Tokudaiaosimensis); 531. Tokunoshima Spiny Rat (Tokudaia tokunoshimensis).

FIGURE 5 in Halosbaena okinawaensis, a new species of Thermosbaenacea (Crustacea) from submarine cave on Okinawa Island, Ryukyu Islands, southwestern Japan

FIGURE 5. Halosbaena okinawaensis sp. nov. A, holotype male, B, paratype female (KMNH IvR 500926), C, paratype female (KMNH IvR 500928): A left pleopods 2 and 3, lateral; B telson and right uropod, dorsal (article 2 of outer ramus was broken); C telson and right uropod, dorsal. Scale = 100 µm.

FIGURE 4 in Halosbaena okinawaensis, a new species of Thermosbaenacea (Crustacea) from submarine cave on Okinawa Island, Ryukyu Islands, southwestern Japan

FIGURE 4. Halosbaena okinawaensis sp. nov. A, B, holotype male, C, paratype female (KMNH IvR 500926), D, E, paratype juvenile (KMNH IvR 500928): A, right pereiopod 6, lateral; B, left pereiopod 7, medial; C, left pereiopod 7, lateral; D, right pereiopod 5, medilal; E, right pereiopod 6, medial. Scale = 100 µm.

FIGURE 1 in Halosbaena okinawaensis, a new species of Thermosbaenacea (Crustacea) from submarine cave on Okinawa Island, Ryukyu Islands, southwestern Japan

FIGURE 1. Halosbaena okinawaensis sp. nov. A, F, paratype juvenile (KMNH IvR 500928), B–D, G, H, holotype male, E, paratype female (KMNH IvR 500926): A, habitus, lateral; B, right antenna 1, dorsal; C, left antenna 2, dorsal; D–F, ocular scales, dorsal; G, left mandible, ventral; H, right mandible, medial. Scales = 100 µm.

FIGURE 3 in Halosbaena okinawaensis, a new species of Thermosbaenacea (Crustacea) from submarine cave on Okinawa Island, Ryukyu Islands, southwestern Japan

FIGURE 3. Halosbaena okinawaensis sp. nov. A–D, holotype male: A, left pereiopod 2, lateral; B, left pereiopod 3, lateral; C, left pereiopod 4, medial; D, right pereiopod 5, lateral. Scale = 100 µm.