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FIGURE 2 in Two new species of Syllidae (Annelida: Polychaeta) from DIVA-Artabria I project (cruise 2002) to deep areas off NW Spain
FIGURE 2. Eurysyllis mercuryi sp. nov. A. Anterior compound chaetae; B. Anterior acicula; C. Midbody compound chaetae; D. Midbody acicula; E. Posterior compound chaetae; F. Ventral simple chaeta; G. Posterior acicula. Scales: 37 μm.
Subspecies and Distribution. M. n. nivalis Linnaeus, 1766 — China, North and South Korea, Mongolia, Russia, Taiwan, and Scandinavia. M. n. allegheniensis Rhoads, 1900 — NE USA (Allegheny Mts W to Wisconsin). M. n. boccamela Bechstein, 1800 — Corsica, Italy, Portugal, Sardinia, Sicily, and Spain. M. n. campestris Jackson, 1913 — C Great Plains, USA. M. n. eskimo Stone, 1900 — Alaska and NW Canada (Yukon). M. n. namiyer Kuroda, 1921 — Japan and the Kurile Is. M. n. numidica Pucheran, 1855 — N Africa. M. n. rnixosa Bangs, 1896 — Canada and N Great Plains of USA. M. n. vulgaris Erxleben, 1777 = W & C Europe and most of C Eurasia. Introduced to New Zealand, Malta, Crete, the Azores Is, and apparently also Sao Tome I. in Mustelidae
Subspecies and Distribution. M. n. nivalis Linnaeus, 1766 — China, North and South Korea, Mongolia, Russia, Taiwan, and Scandinavia. M. n. allegheniensis Rhoads, 1900 — NE USA (Allegheny Mts W to Wisconsin). M. n. boccamela Bechstein, 1800 — Corsica, Italy, Portugal, Sardinia, Sicily, and Spain. M. n. campestris Jackson, 1913 — C Great Plains, USA. M. n. eskimo Stone, 1900 — Alaska and NW Canada (Yukon). M. n. namiyer Kuroda, 1921 — Japan and the Kurile Is. M. n. numidica Pucheran, 1855 — N Africa. M. n. rnixosa Bangs, 1896 — Canada and N Great Plains of USA. M. n. vulgaris Erxleben, 1777 = W & C Europe and most of C Eurasia. Introduced to New Zealand, Malta, Crete, the Azores Is, and apparently also Sao Tome I.
Subspecies and Distribution. N. v. vison Schreber, 1776 — E Canada and NE USA (Allegheny Mts). N. v. aestuarina Grinnell, 1916 — SW USA (California & W Nevada). N. v. aniakensis Burns, 1964 — W Alaska. N. v. energumenos Bangs, 1896 — W Canada and NW USA. N. v. evagor Hall, 1932 — SW Canada (Vancouver I). N. v. evergladensis Hamilton, 1948 — SE USA (SW Florida). N. v. ingens Osgood, 1900 — most of Alaska and NW Canada (N Mackenzie & Yukon). N. v. lacustris Preble, 1902 — C Canada (Keewatin Region, Manitoba & Ontario). N. v. letifera Hollister, 1913 — Great Plains of USA. N. v. low Anderson, 1945 — E Canada (Labrador & Quebec). N. v. lutensis Bangs, 1898 — USA (S Carolina to Florida). N. v. melampeplus Elliot, 1903 — Alaska (Kenai Peninsula). N. v. mink Peale & Palisot de Beauvois, 1796 — SE USA. N. v. nesolestes Heller, 1909 — SW Alaska. N. v. vulgivaga Bangs, 1895 — USA (Arkansas & Louisiana). Introduced to Belarus, Belgium, China, Czech Republic, Denmark, Estonia, Finland, France, Germany, Great Britian, Iceland, Ireland, Italy, Japan (Hokkaido), Latvia, Lithuania, Netherlands, Norway, Poland, Portugal, Russia, Spain, and Sweden. in Mustelidae
Subspecies and Distribution. N. v. vison Schreber, 1776 — E Canada and NE USA (Allegheny Mts). N. v. aestuarina Grinnell, 1916 — SW USA (California & W Nevada). N. v. aniakensis Burns, 1964 — W Alaska. N. v. energumenos Bangs, 1896 — W Canada and NW USA. N. v. evagor Hall, 1932 — SW Canada (Vancouver I). N. v. evergladensis Hamilton, 1948 — SE USA (SW Florida). N. v. ingens Osgood, 1900 — most of Alaska and NW Canada (N Mackenzie & Yukon). N. v. lacustris Preble, 1902 — C Canada (Keewatin Region, Manitoba & Ontario). N. v. letifera Hollister, 1913 — Great Plains of USA. N. v. low Anderson, 1945 — E Canada (Labrador & Quebec). N. v. lutensis Bangs, 1898 — USA (S Carolina to Florida). N. v. melampeplus Elliot, 1903 — Alaska (Kenai Peninsula). N. v. mink Peale & Palisot de Beauvois, 1796 — SE USA. N. v. nesolestes Heller, 1909 — SW Alaska. N. v. vulgivaga Bangs, 1895 — USA (Arkansas & Louisiana). Introduced to Belarus, Belgium, China, Czech Republic, Denmark, Estonia, Finland, France, Germany, Great Britian, Iceland, Ireland, Italy, Japan (Hokkaido), Latvia, Lithuania, Netherlands, Norway, Poland, Portugal, Russia, Spain, and Sweden.
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.
Subspecies and Distribution. E.i.isabellinusTemminck,1840—NEAlgeria,Tunisia,andNWLibya. E. i. boscai Cabrera, 1904 — S Portugal, S Spain, N & C Morocco, NW Algeria, and Canary Is (Lanzarote I). in Vespertilionidae
Subspecies and Distribution. E.i.isabellinusTemminck,1840—NEAlgeria,Tunisia,andNWLibya. E. i. boscai Cabrera, 1904 — S Portugal, S Spain, N & C Morocco, NW Algeria, and Canary Is (Lanzarote I).
Subspecies and Distribution. N. n. noctula Schreber, 1774 — throughout Europe from Great Britain, France, and Spain E to W Russia, W Kazakhstan, and SW Turkmenistan, including S Scandinavia, Gotland and Oland Is, and Cyprus (Cyprus records somewhat tentatively regarded as this subspecies). Absent throughout much of Iberia and is locally extinct in Portugal. N. n. lebanoticus D. L.. Harrison, 1962 — WC & SW Syria, Lebanon, and NE Israel. N. n. mecklenburzevi Kuzyakin, 1934 — SC & E Kazakhstan, SC Russia, W Uzbekistan, Tajikistan, Kyrgyzstan, and NW China (Xinjiang). The species may be present in N Africa, with two records claimed from Algeria in 1858, but these may represent N. lasiopterus; further sampling is needed. in Vespertilionidae
Subspecies and Distribution. N. n. noctula Schreber, 1774 — throughout Europe from Great Britain, France, and Spain E to W Russia, W Kazakhstan, and SW Turkmenistan, including S Scandinavia, Gotland and Oland Is, and Cyprus (Cyprus records somewhat tentatively regarded as this subspecies). Absent throughout much of Iberia and is locally extinct in Portugal. N. n. lebanoticus D. L.. Harrison, 1962 — WC & SW Syria, Lebanon, and NE Israel. N. n. mecklenburzevi Kuzyakin, 1934 — SC & E Kazakhstan, SC Russia, W Uzbekistan, Tajikistan, Kyrgyzstan, and NW China (Xinjiang). The species may be present in N Africa, with two records claimed from Algeria in 1858, but these may represent N. lasiopterus; further sampling is needed.
Subspecies and Distribution. A.l.lerviaPallas,1777—Morocco,NA.l.,andNTunisia. A.l.angusiRothschild,1921—NWNiger(Air&TermitMassifs). A.l.blaineiRothschild,1913—SELybia,NEChad,andNW&NESudan(probablynowrestrictedtoRedSeahills). A.l.fassiniLepri,1930—NWLibya,extremeSTunisia. A.l.ornatus1.GeoffroySaint-Hilaire,1827—SE&SWEgypt. A. l. sahariensis Rothschild, 1913 — S Morocco, Western Sahara, NW Mauritania, S A.l ria, extreme S Libya, NE Mali, SE Niger, and NW Chad. Introduced, free-ranging populations occur in S Spain, the Canary Is, USA (California, New Mexico, and Texas), and NE Mexico. Subspecies of free-ranging introduced populations are unknown because they originate from zoo animals of uncertain origin or from hybrids. Most introduced populations are probably from subspecies lervia, derived from European zoos. The Aoudad has become a widespread invasive species. in Bovidae
Subspecies and Distribution. A.l.lerviaPallas,1777—Morocco,NA.l.,andNTunisia. A.l.angusiRothschild,1921—NWNiger(Air&TermitMassifs). A.l.blaineiRothschild,1913—SELybia,NEChad,andNW&NESudan(probablynowrestrictedtoRedSeahills). A.l.fassiniLepri,1930—NWLibya,extremeSTunisia. A.l.ornatus1.GeoffroySaint-Hilaire,1827—SE&SWEgypt. A. l. sahariensis Rothschild, 1913 — S Morocco, Western Sahara, NW Mauritania, S A.l ria, extreme S Libya, NE Mali, SE Niger, and NW Chad. Introduced, free-ranging populations occur in S Spain, the Canary Is, USA (California, New Mexico, and Texas), and NE Mexico. Subspecies of free-ranging introduced populations are unknown because they originate from zoo animals of uncertain origin or from hybrids. Most introduced populations are probably from subspecies lervia, derived from European zoos. The Aoudad has become a widespread invasive species.
Subspecies and Distribution. C.r.russulaHermann,1780—W&SWEuropeinGermany,Belgium,Netherlands,Luxembourg,N&WSwitzerland,France,Spain,Portugal,andmanycloseoffshoreislands.ApopulationhasbecomeestablishedonGranCanariaIintheCanaryIs,althoughwhenthespecieswaslikelyintroducedisunresolved. C. r. yebalensis Cabrera, 1913 — NW Africa in N Morocco and N Algeria. The Greater White-toothed Shrew has also been recently reported in S Ireland, where it was likely recently introduced, probably representing the subspecies russula. They also seem to have made it to Scilly Is and the Channel Is, where they probably traveled by boat. in Soricidae
Subspecies and Distribution. C.r.russulaHermann,1780—W&SWEuropeinGermany,Belgium,Netherlands,Luxembourg,N&WSwitzerland,France,Spain,Portugal,andmanycloseoffshoreislands.ApopulationhasbecomeestablishedonGranCanariaIintheCanaryIs,althoughwhenthespecieswaslikelyintroducedisunresolved. C. r. yebalensis Cabrera, 1913 — NW Africa in N Morocco and N Algeria. The Greater White-toothed Shrew has also been recently reported in S Ireland, where it was likely recently introduced, probably representing the subspecies russula. They also seem to have made it to Scilly Is and the Channel Is, where they probably traveled by boat.
Distribution. Widely distributed in Europe, from Britain and N Spain E to the Ural Mts (Russia), Turkey, W Syria, Lebanon, N Israel, NW Jordan, Armenia, and W Iran (Zagros Mts). in Muridae
Distribution. Widely distributed in Europe, from Britain and N Spain E to the Ural Mts (Russia), Turkey, W Syria, Lebanon, N Israel, NW Jordan, Armenia, and W Iran (Zagros Mts).
FIGURE 19 in Rissoidae gastropods of the outer continental shelf and slope off Galicia (NW Spain)
FIGURE 19. Obtusella macilenta (Monterosato, 1880). a Shell (0.84 mm) (VE:GA-EBS 150); b Shell (0.86 mm) (VE: GAEBS 150); c Protoconch; d–e Detail of its microsculpture and protoconch/teleoconch transition; f–g Apical view of the protoconch and detail of its embryonic shell.
FIGURE 16 in Rissoidae gastropods of the outer continental shelf and slope off Galicia (NW Spain)
FIGURE 16. Pseudosetia amydralox Bouchet& Warén, 1993. a–b Shell (1.6 mm) and lateral view of its protoconch (DA-I(03): EBS-600); c–d Shell (1.6 mm) and lateral view of its protoconch (DA-I(03): EBS-600); e–f Shell (1.7 mm) and lateral view of its protoconch (SE: DRN-7C); g–j Apical view of two protoconchs and details of their microsculpture; k Shell (1.9 mm) (DAI(03): EBS-600); l–m lateral view of its protoconch and detail of its microsculpture; n Detail of the sculpture of the teleoconch from k; o Shell (1.6 mm) (SE; DRN-7C); p–q Lateral view of its protoconch and detail of its microsculpture; r Suture of the teleoconch; s Peripheral micro-cord.
FIGURE 15 in Rissoidae gastropods of the outer continental shelf and slope off Galicia (NW Spain)
FIGURE 15. Gofasia thalassae (Bouchet & Warén, 1993) comb. nov. a Shell (2.8 mm); b–c Details of its microsculpture (DAI(03): DRN-1000); d Shell (2.6 mm); e Its protoconch; f Details of its microsculpture (VE: GA-EBS-600); g Shell (2.6 mm); h Apical view of its protoconch (VE: GA-EBS-600).
FIGURE 12 in Rissoidae gastropods of the outer continental shelf and slope off Galicia (NW Spain)
FIGURE 12. Alvania cancapae Bouchet & Warén, 1993 (SE: AT12). a Shell (2.0 m); b–c Protoconch in lateral and apical view; d Detail of microsculpture of the protoconch; e–f Detail of microsculpture of the teleoconch.
FIGURE 13 in Rissoidae gastropods of the outer continental shelf and slope off Galicia (NW Spain)
FIGURE 13. Alvania candasae Oliver & Gofas sp. nov. Holotype (DA-II(08): DRNp-26). a Shell (1.85 mm); b Lateral view of its protoconch; c Apical view of the protoconch; d Detail of its microsculpture; e Detail of the microsculpture of the subsutural furrow. Paratypes 4 and 5 (DA-II(08): EBS-15). f–k Paratype 4; f Shell (1.7 mm); g Lateral view of its protoconch; h–i Details of its microsculpture; j–k Details of microsculpture of the teleoconch; l–o Paratype 5; l Shell (1.8 mm); m–n Protoconch and detail of its microsculpture; o Detail of the sculpture of the teleoconch in the subsutural area.
FIGURE 10. a–d in Rissoidae gastropods of the outer continental shelf and slope off Galicia (NW Spain)
FIGURE 10. a–d Alvania sp. from Djibouti Bank (Alborán Sea). a Shell (1.8 mm); b–c Protoconch, lateral and apical view; d Detail of the protoconch/teleoconch transition. e–g Alvania cf. elegantissima off Italian coast of the Tyrrhenian Sea; e Shell (1.6 mm); f Apical view of the protoconch; g Detail of the axial ribs and spiral sculpture.
FIGURE 9 in Rissoidae gastropods of the outer continental shelf and slope off Galicia (NW Spain)
FIGURE 9. Alvania electa (Monterosato, 1874) (VE:GA-EBS-600). a Shell (1.8 mm); b–c Protoconch from a and detail of its microsculpture; d–e Details of microsculpture of the teleoconch of figure a; f Shell (1.7 mm); g–h Lateral view of the protoconch from f and detail of its microsculpture; i Apical view of another protoconch.
FIGURE 7 in Rissoidae gastropods of the outer continental shelf and slope off Galicia (NW Spain)
FIGURE 7. Alvania zetlandica (Montagu, 1815) (SA: SARRI-2). a Shell (2.9 mm); b Protoconch; c Detail of the protoconch/ teleoconch transition; d Detail of the microsculpture of the embryonic protoconch; e–f–g Details of the microsculpture of the teleoconch.
FIGURE 21 in Rissoidae gastropods of the outer continental shelf and slope off Galicia (NW Spain)
FIGURE 21. Pusillina cf. radiata (Philippi, 1836). a–b Juvenile eroded shells (a: 1.6 mm; b: 1.7 mm) (SE:DRN-7); c Protoconch (VE:GA-AT-800); d Alvania cancellata (Da Costa, 1778) (0.96 mm) (VE:AG-EBS-150); e Crisilla semistriata (Montagu, 1808) (1.9 mm) (SE-08:EBS14); f Onoba semicostata (Montagu, 1803) (1.7 mm) (SA:SARRI-3); g Manzonia crassa (Kanmacher, 1798) (2.1 mm) (SE:DRN7).
FIGURE 6 in Rissoidae gastropods of the outer continental shelf and slope off Galicia (NW Spain)
FIGURE 6. Alvania subsoluta (Aradas, 1847) (DA-II (08):EBS-27). a Shell (2.7 mm); b Shell (2.3 mm); c Shell (2.1 mm); d–e Protoconch from a; f Lateral view of the protoconch from c; g Detail of the microsculpture of protoconch; h Detail of the microsculpture of teleoconch.
FIGURE 18 in Rissoidae gastropods of the outer continental shelf and slope off Galicia (NW Spain)
FIGURE 18. Obtusella intersecta (S.V. Wood,1857) (VE:AG-EBS-150). a–c Shell (1.0 mm), lateral view of its protoconch and microsculpture of the teleoconch; d–e Shell (0.9 mm) and microsculpture of its protoconch; f–g Embryonic protoconch and detail of its microsculpture.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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OpenNeuro
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