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FIGURE 2 in A new species and new record of deep-sea scale-worms (Polynoidae: Polychaeta) from the Okinawa Trough and the South China Sea
FIGURE 2. Branchipolynoe pettiboneae Miura & Hashimoto, 1991. a. Anterior end, dorsal view (one palplost). b. Same, ventral view. c. Second parapodia. d. Sixth parapodia. Scale bars=1mm.
FIGURE 1 in A new species and new record of deep-sea scale-worms (Polynoidae: Polychaeta) from the Okinawa Trough and the South China Sea
FIGURE 1. Branchipolynoe pettiboneae Miura & Hashimoto, 1991. a. Anterior end, dorsal view (one palplost). b. Same, ventral view. c. Ventral view of papillae on segments 11 and 12. d. Dorsal view of posterior end showing elytra and large, arborescent branchiae again label these with an arrow (Anal cirri lost). Scale bars=1mm.
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.
FIGURE 3. Polyonyx deezi n in A distinctive new species of the genus Polyonyx Stimpson, 1858 (Crustacea Decapoda: Anomura: Porcellanidae) from Okinawa, southwestern Japan
FIGURE 3. Polyonyx deezi n. sp., holotype, (cl 2.3 mm, cw 3.0 mm), RUMF-ZC 7601. A, smaller cheliped, merus to chela, dorsal view (only soft plumose setae on dorso-anterior surface of chela drawn); B, same, distal part of chela, perpendicular ventral view; C, left second pereopod, lateral view; D, same, merus, mesial view; E, same, dactylus and distal part of propodus, lateral view (setae not drawn); F, right second pereopod, propodus, lateral view (setae not drawn); G, left third pereopod, lateral view (granules, ridges, and setae not drawn); I, left fourth pereopod, lateral view (granules, ridges, and setae not drawn). Plumose setae shown simplified. Scale bars = 1.0 mm.
FIGURE 1. Polyonyx deezi n in A distinctive new species of the genus Polyonyx Stimpson, 1858 (Crustacea Decapoda: Anomura: Porcellanidae) from Okinawa, southwestern Japan
FIGURE 1. Polyonyx deezi n. sp., holotype, (cl 2.3 mm, cw 3.0 mm), RUMF-ZC 7601. A, carapace and ocular and antennal peduncles, dorsal view (granules and setae drawn only on left side); B, carapace, pterygostomial flap, and ocular and antennal peduncles, left lateral view; C, rostrum, dorso-anterior view; D, third and fourth thoracic sternites, ventral view (setae drawn only on right side); E, telson, external view; F, left basal article of antennular peduncle, ventral view; G, left ocular and antennal peduncles and anterolateral part of carapace, dorsal view; H, left ocular peduncle and first article of antennal peduncle, lateroanterior view; I, left third maxilliped, coxa to merus and exopod, lateral view (for setae, only soft plumose setae drawn); J, same, merus to dactylus, lateral view (setae not drawn). Plumose setae shown simplified. Scale bars = 1.0 mm.
FIGURE 4. Polyonyx deezi n in A distinctive new species of the genus Polyonyx Stimpson, 1858 (Crustacea Decapoda: Anomura: Porcellanidae) from Okinawa, southwestern Japan
FIGURE 4. Polyonyx deezi n. sp., holotype, (cl 2.3 mm, cw 3.0 mm), RUMF-ZC 7601. Entire animal, dorsal view.
FIGURE 2. Polyonyx deezi n in A distinctive new species of the genus Polyonyx Stimpson, 1858 (Crustacea Decapoda: Anomura: Porcellanidae) from Okinawa, southwestern Japan
FIGURE 2. Polyonyx deezi n. sp., holotype, (cl 2.3 mm, cw 3.0 mm), RUMF-ZC 7601. Left larger cheliped. A, entire, dorsal view; B, carpus and distal part of merus, perpendicular dorsal view; C, chela, perpendicular dorsal view; D, entire, ventral view; E, chela, anterior margin, ventro-anterior view; F, distal part of chela, perpendicular ventral view. For setae, only soft plumose setae drawn and shown simplified. Scale bar = 1.0 mm.
FIGURE 9 in Maerid amphipods (Crustacea: Amphipoda) from Okinawa, Japan with description of a new species
FIGURE 9. Elasmopus mukuinu sp. nov., paratype female, 4.2 mm. A, gnathopod 1, lateral; B, gnathopod 2, medial; C, telson; D, gnathopod 2, lateral; E, gnathopod 1, medial. Scale bars: 0.5 mm.
FIGURE 8 in Maerid amphipods (Crustacea: Amphipoda) from Okinawa, Japan with description of a new species
FIGURE 8. Elasmopus mukuinu sp. nov., paratype male, 5.1 mm. A, right mandible; E, upper lip. Holotype male, 6.1 mm. B, maxilla 2; C, maxilla 1; D, left mandible; F, lower lip; G, maxilliped. Scale bars: 0.5 mm.
FIGURE 7 in Maerid amphipods (Crustacea: Amphipoda) from Okinawa, Japan with description of a new species
FIGURE 7. Elasmopus mukuinu sp. nov., holotype male, 6.1 mm. A, pereopod 3; B, pereopod 4; C, pereopod 7; D, pereopod 5. Scale bar: 0.5 mm.
FIGURE 6 in Maerid amphipods (Crustacea: Amphipoda) from Okinawa, Japan with description of a new species
FIGURE 6. Elasmopus mukuinu sp. nov., holotype male, 6.1 mm. A, gnathopod 1, lateral; B, pereopod 6; C, gnathopod 1, medial; D, telson. Scale bars: 0.5 mm.
FIGURE 5 in Maerid amphipods (Crustacea: Amphipoda) from Okinawa, Japan with description of a new species
FIGURE 5. Elasmopus mukuinu sp. nov., holotype male, 6.1 mm. A, uropod 3; B, uropod 2; C, uropod 1; D, epimeron 3 posteroventral corner; E, gnathopod 2, medial; F, enlarged plumose seta from carpus; G, enlarged plumose seta on propodus; H, gnathopod 2 propodus palm, setae removed. Scale bars: 0.5 mm (A–E, H), 0.1 mm (F,G).
FIGURE 4 in Maerid amphipods (Crustacea: Amphipoda) from Okinawa, Japan with description of a new species
FIGURE 4. Elasmopus mukuinu sp. nov., holotype male, 6.1 mm. A, habitus; B, antenna 1 accessory flagellum; C, head. paratype male, 4,7 mm. D, telson. Scale bars: 0.5 mm (A, C), 0.1 mm (B, D).
FIGURE 2 in Maerid amphipods (Crustacea: Amphipoda) from Okinawa, Japan with description of a new species
FIGURE 2. Ceradocus mizani Lim, Azman & Othman, 2010 male, 8.7 mm. A, gnathopod 1, medial; B, telson; C, small gnathopod 2, medial; D, large gnathopod 2, medial; E, epimera 1–3; F, pleonite 1, dorsal; G, pleonite 2. Dorsal; H, pleonite 3, dorsal; I, urosomite 1, dorsal; J, urosomite 2, dorsal. Scale bars: 0.5 mm.
Subspecies and Distribution. P. d. dasymallus Temminck, 1825 — Osumi and Tokara Is (Kuchinoerabujima, Kuchinoshima, Nakanojima, Suwanosejima, Tairajima, Akusekijima, Takarajima), N Ryukyu Is, Japan. P. d. daitoensis Kuroda, 1921 — Daito Is (Kita-Daito, Minami-Daitd), E Ryukyu Is, Japan. P. d. formosus Sclater, 1873 — Taiwan (Lutao, Lanyu, and Guishan Dao Is) and Philippines (Batan, Babuyan, Calayan, Dalupiri, Fuga, and Barit Is). Probably extinct on Taiwan mainland. P. d. inopinatus Kuroda, 1933 — Anami and Okinawa Is (Okinawajima, Izenajima, Kourijima, Iejima, Minnajima, Ikeijima, Henzajima, Hamahigajima, Kudakajima, Agunijima, Iheyajima, Yoronjima, Tokasikijima), C Ryukyu Is, Japan. P. d. yayeyamae Kuroda, 1933 — Miyako and Yaeyama Is (Ishigakijima, Iriomotejima, Kohamajima, Hatomajima, Taketomijima, Haterumajima, Kurojima, Yonagunijima, Aragusukujima, Taramajima, Irabujima, Miyakojima, Ikemajima, Ogamijima, Kurimajima, Shimonjijima), S Ryukyu Is, Japan. in Pteropodidae
Subspecies and Distribution. P. d. dasymallus Temminck, 1825 — Osumi and Tokara Is (Kuchinoerabujima, Kuchinoshima, Nakanojima, Suwanosejima, Tairajima, Akusekijima, Takarajima), N Ryukyu Is, Japan. P. d. daitoensis Kuroda, 1921 — Daito Is (Kita-Daito, Minami-Daitd), E Ryukyu Is, Japan. P. d. formosus Sclater, 1873 — Taiwan (Lutao, Lanyu, and Guishan Dao Is) and Philippines (Batan, Babuyan, Calayan, Dalupiri, Fuga, and Barit Is). Probably extinct on Taiwan mainland. P. d. inopinatus Kuroda, 1933 — Anami and Okinawa Is (Okinawajima, Izenajima, Kourijima, Iejima, Minnajima, Ikeijima, Henzajima, Hamahigajima, Kudakajima, Agunijima, Iheyajima, Yoronjima, Tokasikijima), C Ryukyu Is, Japan. P. d. yayeyamae Kuroda, 1933 — Miyako and Yaeyama Is (Ishigakijima, Iriomotejima, Kohamajima, Hatomajima, Taketomijima, Haterumajima, Kurojima, Yonagunijima, Aragusukujima, Taramajima, Irabujima, Miyakojima, Ikemajima, Ogamijima, Kurimajima, Shimonjijima), S Ryukyu Is, Japan.
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.
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).
FIGURES 9–10 in A warmth-loving brother of northern siblings: the first subtropical species of Forinus Kurbatov discovered on Okinawa-jima Japan (Coleoptera, Staphylinidae, Pselaphinae)
FIGURES 9–10. Forinus mirus sp. n., male. Metacoxal region in ventral view (9); distal region of left middle leg in dorsal view (10). Abbreviations: cxp, coxal process; msp, median sternal process; sIII‒IV, sternite III‒IV; v3, metaventrite.
FIGURES 1–2 in A warmth-loving brother of northern siblings: the first subtropical species of Forinus Kurbatov discovered on Okinawa-jima Japan (Coleoptera, Staphylinidae, Pselaphinae)
FIGURES 1–2. Forinus mirus sp. n., male. Dorsal habitus (1); distribution of all nominal Forinus species with aedeagi in lateral view compared (illustrations for F. macer and F. secundus after Kurbatov (1991, 1992), respectively) (2).
FIGURES 7–8 in A warmth-loving brother of northern siblings: the first subtropical species of Forinus Kurbatov discovered on Okinawa-jima Japan (Coleoptera, Staphylinidae, Pselaphinae)
FIGURES 7–8. Forinus mirus sp. n., male. Left elytron in dorsal view (7); pterothorax and abdominal base in ventral view (8). Abbreviations: bef, basal elytral foveae; ds, discal sulcus; ss, sutural sulcus; v2, mesoventrite; v3, metaventrite. Arrowheads indicate foveae.
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