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Mauretanaspis longichaeta gen. et spec. nov. urn:lsid:zoobank.org:act: AA378791-074B-4349-B2E2-235FD632E35C Figs 1���4, Table 1 Etymology The species epithet is a combination of the Latin ��� longus ��� (= ���long���) and the Greek ��� chaeta ��� (= ���bristle���) characterizing the striking length of the posteriormost lateral chaetae of the ventro-caudal shield. Material examined Holotype NORTHEAST ATLANTIC ��� Off Mauritania ��� 1 complete specimen (body slightly contracted, introvert fully everted, length 5.0 mm, width 1.6 mm, abdomen length 3.0 mm, left shield plate length 1.2 mm, width 0.9 mm); Block C9, stn C9-15 (B3); 18��21.27��� N, 17��57.44��� W; depth 2712 m; 24 Oct. 2018; deepsea mud, box core; MNHN-IA-TYPE 2005. Paratype NORTHEAST ATLANTIC ��� Off Mauritania ��� 1 complete specimen (introvert partly retracted, length 3.5 mm, width 1.8 mm, abdomen length 1.0 mm, left shield plate length 1.2 mm, width 1.2 mm); Block C9, stn C9-15 (B1); 18��21.27��� N, 17��57.44��� W; depth 2712 m; 24 Oct. 2018; deep-sea mud, box core; SMF 27777. Other material NORTHEAST ATLANTIC ��� Off Mauritania ��� 1 spec. (bad condition, anterior end retracted, length n.d., width 2.6 mm, abdomen length 3.7 mm, left shield plate length 1.6 mm, width 1.0 mm); Block C9, stn C9-20 (B1); 18��26.91��� N, 17��59.25��� W; depth 2714 m; 27 Oct. 2018; deep-sea mud, box core; SMF 27776. SOUTHEAST ATLANTIC ��� Off Angola ��� 1 spec. (juvenile with capillary chaetae in pre-shield segments, without gonopodial lobes, anterior end missing, length n.d., width 0.35 mm); stn S48-03A; 6��53.107��� S, 10��30.762��� E; depth 2935 m; 7 Sep. 2018; box core; MNHN-IA-PNT 120 ��� 1 spec. (juvenile, anterior end damaged, length n.d., width 0.65 mm, left shield plate length 0.5 mm); stn S48-08A; 6��59.047��� S, 10��36.748��� E; depth 2736 m; 9 Sep. 2018; box core; SMF 28061 ��� 1 spec. (gonopodial lobes present, length 3.2 mm, width 1.1 mm, left shield plate length 1.1 mm); stn S48-09C; 7��4.931��� S, 10��13.003��� E; depth 4373 m; 14 Sep. 2018; box core; SMF 28062 ��� 1 spec. (juvenile, body wall translucent, with chaetae in some abdominal segments, without gonopodial lobes, length 2.5 mm, width 0.9 mm); stn S48-14C; 7��10.998��� S, 10��13.064��� E; depth 4363 m; 14 Sep. 2018; box core; MNCN 16.01/18762 ��� 1 spec. (strongly bent and wrinkled, gonopodial lobes not seen, posteriormost lateral chaetae ca 4�� length of body, length n.d., width n.d., left shield plate length 1.0 mm); stn S48-23A; 7��23.159��� S, 10��24.921��� E; depth 4375 m; 15 Sep. 2018; box core; MNCN 16.01/18763 ��� 1 spec. (juvenile, body wall translucent, anterior end missing); stn S48-23B; 7��23.159��� S, 10��24.921��� E; depth 4375 m; 15 Sep. 2018; box core; DBUA0002349.01 ��� 1 spec. (anterior end retracted, gonopodial lobes retracted but visible, length n.d., width n.d., left shield plate length 1.0 mm); stn S48-26C; 6��58.715��� S, 10��17.741��� E; depth 4191 m; 10 Sep. 2018; box core; DBUA0002349.02. Description Based on holotype (Figs 1, 2 A���C, 3A���C), complete specimen (body slightly contracted but introvert fully everted), complemented by paratype (Fig. 4 A���C) where indicated. BODY COLOUR. Pale yellow. PROSTOMIUM. Small hemispherical cupule, pale, semi translucent. Eyes absent. PERISTOMIUM. Surrounding mouth projecting to level of prostomial cupule, about 1.5 �� diameter of prostomium. Mouth small, round. INTROVERT. First three chaetigers each with 15���17 hooks on either side (segment 1: left 9 +6 small, right 8 +8; 2: left 9+ 7, right 9 +8; 3: left 9+6, right 8+7); hooks golden, tapering to blunt transparent tip; decreasing gradually in length and diameter from dorsal to ventral in each fascicle. Ventralmost 6���8 hooks small to minute. Hooks equally spaced in fully everted introvert (Figs 1, 2 A���C, 3A, 4A). Minute drop-shaped papillae in single rows parallel to segmental folds dorsally in segments 1���3. Body damaged ventrally on segments 3���4 with oesophagus protruding (Figs 1, 2C, 3A). Gonopodial lobes small, digitiform, protruding ventrolaterally from intersegmental groove between segments 5 and 6 (Figs 1, 4 A���B). ANTERIOR ABDOMEN (PRE- SHIELD REGION). Comprising eight segments. Body papillae minute, round, forming single rows close to intersegmental folds, sometimes obscured by sediment particles (Figs 1, 4B). Most pre-shield segments of holotype with smooth median surface on ventral side, possibly abraded, and few, short, filamentous papillae on lateral sides; in paratype median surface papillated (Figs 1, 4A). Few filamentous papillae among adhering sediment particles on segments anterior to branchial plates. VENTRO- CAUDAL SHIELD. Densely covered by fine, firmly adhering sediment particles. Shield colour light brown, obscured by dense cover of sediment. Colour most intense around anterior end of median suture (sediment abraded in holotype, not abraded in paratype) (Figs 3B, 4A). No structures (ribs, concentric rings) visible due to sediment cover. Anterior margins slightly rounded, anterior depression shallow, covered by sediment; anterior keels faintly visible (Fig. 3B), not exposed. Lateral margins rounded, strongly bent towards dorsal side, not forming free, stiff or pliable margins, but rather merging into integument. Posterior fan and lateral notch not discernible due to sediment cover; shallow median notch (more pronounced in paratype (Fig. 4A, C)). Suture defined in anterior �� of shield, moderately deep with distinct lateral borders (Figs 3B, 4A). MARGINAL SHIELD CHAETAE. Yellow; 20 lateral fascicles, i.e., 9���11 fascicles per side, with 4���6 capillary chaetae each. Chaetae arranged in oblique rows, increasing gradually in length posteriorly within each fascicle and among fascicles (Figs 2C, 3C, 4 B���C); chaetae of posteriormost lateral fascicle very long, equalling body length (Figs 2C, 3D). Six pairs of fascicles posterior to shield (i.e., posterior shield chaetae), each with 1���3 (mostly 2) yellow capillaries of varying length and different strength (Figs 3B, 4A, C); lateralmost longest, equalling length of shield. Peg chaetae absent. BRANCHIAL FILAMENTS. Numerous, increasing in length posteriorly, opaque, coiled to various extent. BRANCHIAL PLATES. Brownish, forming ovoid to trapezoidal region, densely covered by filaments, filamentous papillae and sediment grains (Fig. 3C). Distribution Northeast to Southeast Atlantic, from off Mauritania to Angola, in deep-sea mud, in depths of 2700��� 4400 m. Remarks Mauretanaspis longichaeta gen. et spec. nov. can be distinguished from all other known species of Sternaspidae by the following combination of characters: introvert hooks tapering, tips transparent; pre-shield region with eight segments; ventro-caudal shield densely covered with fine, firmly adhering sediment obscuring shield structures except median suture. Mauretanaspis longichaeta gen. et spec. nov. is the only sternaspid with chaetae in posteriormost lateral fascicles equalling body length. In one specimen collected off Angola (MNCN 16.01/18763), posteriormost lateral chaetae even measure about 4�� the length of the body. Several specimens from off Angola (SMF 28062, MNCN 16.01/18762, MNCN 16.01/18763, DBUA0002349.01) show black pigment presumably from surrounding sediment included in sediment cover and among sand grains in the branchial region. Black particles are scattered on the shield forming spots of different sizes. We compared our material to a specimen collected off Northwest Africa in 1320 m depth and identified as Sternaspis scutata (Ranzani, 1817) by Kirkegaard (2001: 396). The specimen, deposited in the collections of the Natural History Museum of Denmark (NHMD 662048), was not available for study, but pictures of it were kindly made available to us by S. Salazar-Vallejo. Unfortunately, the animal is in very bad condition: anterior hooks tapering to fine tips, number of pre-shield segments and gonopodial lobes not distinguishable, shield completely covered by fine sediment obscuring surface structures, shield without free margins, length of lateral and posterior shield chaetae indeterminable. It remains uncertain whether the sediment can be removed from the shield without damaging it, but with regard to shield characters visible in the pictures available, the specimen appears incorrectly identified as Sternaspis scutata. However, due to its bad condition we cannot identify it any further. Identification key to Sternaspidae with sediment particles firmly attached to ventro-caudal shield ( Caulleryaspis (in part) and Mauretanaspis gen. nov.) (adapted from Salazar- Vallejo 2017) 1. Shield with anterior depression deep; peg chaetae robust................................................................ 2 ��� Shield with anterior depression shallow; peg chaetae absent........................................................... 3 2. Shield with anterior margins angular; peg chaetae forming thick, large spines.......................................................... Caulleryaspis gudmundssoni Sendall & Salazar-Vallejo, 2013 (N Atlantic, Iceland) ��� Shield with anterior margins rounded; peg chaetae forming thin, small spines..................................... Caulleryaspis fauchaldi Salazar-Vallejo & Buzhinskaja 2013 (NE Pacific, Oregon to California) 3. Seven pre-shield segments; chaetae in posteriormost lateral fascicles about length of shield............................................... Caulleryaspis laevis (Caullery, 1944) (Indo-Pacific, Indonesia) ��� Eight pre-shield segments; chaetae in posteriormost lateral fascicles equalling body length.......................... Mauretanaspis longichaeta gen. et spec. nov. (NE and SE Atlantic, Mauritania to Angola), Published as part of Fiege, Dieter & Barnich, Ruth, 2020, A new genus and species of Sternaspidae (Annelida: Polychaeta) from the deep eastern Atlantic, pp. 1-13 in European Journal of Taxonomy 699 on pages 4-10, DOI: 10.5852/ejt.2020.699, http://zenodo.org/record/3981057, {"references":["Ranzani C. 1817. Descrizione di una nova specie del genere Thalassema. Opusculi Scientifici I: 112 - 116.","Kirkegaard J. B. 2001. Deep-sea polychaetes from northwest Africa, including the description of a new species of Neopolynoe (Polynoidae). Journal of the Marine Biological Association of the United Kingdom 81: 391 - 397. https: // doi. org / 10.1017 / S 0025315401004003","Sendall K. & Salazar-Vallejo S. I. 2013. Revision of Sternaspis Otto, 1821 (Polychaeta, Sternaspidae). ZooKeys 286: 1 - 74. https: // doi. org / 10.3897 / zookeys. 286.4438","Salazar-Vallejo S. I. & Buzhinskaja G. N. 2013. Six new deep-water sternaspid species (Annelida, Sternaspidae) from the Pacific Ocean. ZooKeys 348: 1 - 27. https: // doi. org / 10.3897 / zookeys. 348.5449","Caullery M. 1944. Polychetes sedentaires de l'expedition du Siboga. Ariciidae, Spionidae, Chaetopteridae, Chlorhaemidae, Opheliidae, Oweniidae, Sabellariidae, Sternaspidae, Amphictenidae, Ampharetidae, Terebellidae. Siboga-Expeditie 24 (2): 1 - 204. Brill, Leiden."]}

Mauretanaspis gen. nov. urn:lsid:zoobank.org:act: 1FC8F8ED-C7A3-4EC9-AB69-6A0147632D23 Table 2 Type species Mauretanaspis longichaeta gen. et spec. nov. designated herein. Diagnosis Sternaspids with introvert hooks tapering. Eight segments between gonopodial lobes and shield (i.e., preshield region). Ventro-caudal shield densely covered with firmly adhering fine sediment, which cannot be brushed off. Due to sediment cover no shield structures like ribs or concentric rings visible except median suture. Shield with lateral margins strongly bent towards dorsal side, merging into integument. Peg chaetae absent. Etymology The genus name is a combination of the Latin name for the type locality off the Northwest African state Mauritania (i.e., Mauretania, Lat.) and the Greek word ��� aspis ��� (= ���shield���); gender: feminine. Remarks Mauretanaspis gen. nov. differs in the combination of characters from the other genera of Sternaspidae. The shield is completely and firmly covered by sediment, as in several species of Caulleryaspis, but it has eight pre-shield segments; peg chaetae (i.e., a dense group of short chaetae covered by a common sheath) are absent, while Caulleryaspis has seven pre-shield segments and peg chaetae are present. In Caulleryaspis nuda peg chaetae are absent, but according to Drennan et al. (2019) this species possibly belongs to the genus Sternaspis (see ���Discussion���). Petersenaspis has eight pre-shield segments and peg chaetae are absent, as in Mauretanaspis gen. nov., but the shield is not covered by sediment and the introvert hooks are subdistally expanded or spatulate while hooks in Mauretanaspis gen. nov. are tapering (Table 2)., Published as part of Fiege, Dieter & Barnich, Ruth, 2020, A new genus and species of Sternaspidae (Annelida: Polychaeta) from the deep eastern Atlantic, pp. 1-13 in European Journal of Taxonomy 699 on page 3, DOI: 10.5852/ejt.2020.699, http://zenodo.org/record/3981057, {"references":["Drennan R., Wiklund H., Rouse G. W., Georgieva M. N., Wu X., Kobayashi G., Yoshino K. & Glover A. G. 2019. Taxonomy and phylogeny of mud owls (Annelida: Sternaspidae), including a new synonymy and new records from the Southern Ocean, North East Atlantic Ocean and Pacific Ocean: challenges in morphological delimitation. Marine Biodiversity 49: 2659 - 2697. https: // doi. org / 10.1007 / s 12526 - 019 - 00998 - 0"]}

Syllis qamhiyn n.sp. Figures 2–6 urn:lsid:zoobank.org:act: A270D267-0901-4185-80E4-E6D0AAC48A49 Material examined. Holotype (SMF 26713) Soc /ST–726, Ras Qataninh Bay, 12º21.293’N 53º32.659’E, under stones and coral rubble, 8–10 m, coll. T. Wehe 9.4.2000. 1 paratype, same collection data (NHCY 0018); 1 paratype prepared for SEM, Soc/ST–725, Ras Qataninh Bay, dredge, 12º21.789’N 53º31.399’E to 12º21.780’N 53º31.390’E, 18–20 m, coll. T. Wehe 09.04.2000, (SMF 26714, SEM-stub 1311). Diagnosis. Conspicuously thick and short dorsal cirri filled with gelatinous substance; reduced number of compound chaetae from midbody to posterior parapodia, with enlarged shafts and short blades, which become almost unidentate; blades not fused to shafts. Description. Holotype complete specimen, 17.5 mm long, 0.69 mm wide, with 151 chaetigers (Fig. 2A). One incomplete paratype with 134 chaetigers, and other complete, Paratype (SMF 26714), 18.5 mm long, 0,5 mm wide, with 160 chaetigers (Fig. 4B). Body long and slender, filiform, without colour pattern (Figs 2A, B, C; 4B). Prostomium semicircular to oval (Figs 2A; 5A); four small eyes in trapezoidal arrangement. Palps similar in length to prostomium. Median antenna arising between anterior eyes, with 12–13 articles, shorter than combined length of prostomium and palps. Lateral antennae same length as median antenna, with 13 articles each (Fig. 2A). Peristomium dorsally shorter than subsequent segments (Figs. 2A; 5B). Dorsal tentacular cirri about 15–21 articles each; ventral tentacular cirri about 13–14 articles each. Dorsal parapodial cirri relatively thin on anterior segments, alternating relatively long (0.3 mm) and short (0.2 mm); longer cirri similar in length to body width at corresponding chaetiger, with about 17–19 articles, shorter ones about 7–11 articles each (Fig. 2A); from midbody posteriorwards, dorsal cirri shorter than body width, each cirrus thicker in midlength, with about eight well-marked articles, with acute article distally (Fig. 2 A–D); most articles of these dorsal cirri filled with gelatinous substance (Fig. 2D), articles covered by small pores (Fig. 5F). Ventral cirri oval, shorter than parapodial lobes (Figs 2D; 6D). Ventral area of parapodia with almost circular area of pores (Fig. 6 C–E) and internal gland (Fig. 2D). Compound chaetae as heterogomph falcigers; anterior parapodia with about 10 falcigers each; falcigers with slender bidentate blades, proximal tooth distinctly shorter than distal one, and short spines on margin; blades with dorsoventral gradation in length, 42–20 μm long (Figs 3A; 5C, D). Number of chaetae per parapodium progressively diminishing posteriorly, 4–5 in midbody (Figs 3C; 5E, G, H) and 3–5 on mid-posterior and posterior parapodia (Figs 3E; 6 A–B), shafts becoming larger and blades shorter and minutely bidentate, with proximal tooth much smaller than distal one (Fig. 3E). Midbody falcigers with blades 20–19 μm long, posterior body falcigers with blades similar, about 19 μm long. Dorsal and ventral simple chaetae not seen. Anterior parapodia with five slender aciculae each, distally rounded (Fig. 3B), three in midbody parapodia (Fig. 3D); posterior parapodia with two distally oblique aciculae each (Fig. 3F). Pharynx long, extending through about 13 segments (Figs 2A; 4B); pharyngeal tooth elongated, conical, acute, on anterior margin of pharynx (Figs 2A, 4A). Proventricle shorter than pharynx, through 9–10 segments (Fig. 2A), with about 48–50 muscle cell bands. Pygidium small, with two anal cirri, with 7–8 articles each (Fig. 6F). Etymology. The name of the species refers to Dendrosicyos socotrana, the only species of Cucurbitaceae growing into tree form and original from Socotra Island. Its trunk resembles the shape of midbody cirri of S. qamhiyn n.sp. In soqotri language it is named qamhiyn. Remarks. Syllis qamhiyn n.sp. is characterized by having short, thick, distally acute dorsal cirri on midbody and posterior parapodia, and reduced number of falcigers in these parapodia, with enlarged shafts and short, almost unidentate blades, not fused to shafts. Syllis qamhiyn n.sp. belongs to the same group of species of Syllis armillaris (O. F. Müller, 1771) and related species, the latter considered cosmopolitan but likely a species complex. The mid- and posterior body falcigers of Syllis armillaris also have almost unidentate blades, but they are not so short and the shafts are not as enlarged as in Syllis qamhiyn n.sp. (San Martín 2003); furthermore, the mid- and posterior body dorsal cirri of Syllis armillaris are enlarged, but not so much as in Syllis qamhiyn n.sp. Similar differences are between Syllis qamhiyn n.sp. and S. pseudoarmillaris Nogueira & San Martín, 2002 from Brazil (Nogueira & San Martín 2002); S. pseudoarmillaris has fewer number of articles on midbody dorsal cirri and the compound chaetae of these parapodia are clearly bidentate, with not enlarged shafts; furthermore, the pharynx and proventricle are longer in S. qamhiyn n.sp. Syllis gracilis Grube, 1840, also considered a cosmopolitan species, and S. picta (Kinberg, 1886), from the Indo-Pacific (including the Red Sea), have similar bodies, with enlarged mid- and posterior body dorsal cirri, but in these species at least one of the compound chaetae on these parapodia have fused blade and shaft (San Martín 2003; Álvarez-Campos et al. 2015; 2017). Habitat. Under stones and coral rubble from 8– 20 m. Distribution. Only known from Socotra Archipelago. Type locality. Ras Qataninh Bay, Socotra Island.

Syllis compacta Gravier 1900 Syllis (Typosyllis) compacta Gravier, 1900: 165, pl. IX, fig. 11, text-fig. 33���38. Syllis compacta.��� L��pez et al. 1996: 110, fig. 3; San Mart��n 2003: 433, figs 238���239. Non Syllis golfonovoensis (Hartman-Sch��der, 1962): 87���89, figs 60���62; San Mart��n 1984: 395, figs 104, 105. Material examined. Rush 009, Samha, 12��10.317���N 53��04.383���E, upper intertidial among algae, coll. T. Wehe 7.4.2000, 2 specimens (SMF 26700). Habitat. Intertidal, amongst algae. Typically found in intertidal pools, specially on calcareous concretions of biological origin, like vermetid reefs, coral blocks, Posidonia oceanica rhizomes, photophilic and sciaphilic algae (L��pez et al. 1996). Distribution. Djibouti, Gulf of Aden (Gravier 1900). Adriatic Sea, Turkish Aegean Sea, Ionian Sea, North West Italy, East and western Mediterranean Sea, North East Atlantic, East coast of Spain (Musco & Giangrande 2005). New record for Socotra. Type locality. Djibouti, Gulf of Aden., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2020, New species and records of the genus Syllis Savigny in Lamarck, 1818 (Annelida: Syllidae) from Socotra Archipelago (Indian Ocean), pp. 73-88 in Zootaxa 4742 (1) on page 78, DOI: 10.11646/zootaxa.4742.1.4, http://zenodo.org/record/3674479, {"references":["Gravier, C. (1900) Contribution a l'etude des annelides polychetes de la Mer Rouge. Premiere partie. Nouvelles Archives du Museum d'Histoire Naturelle, Paris, 2, 137 - 282. https: // doi. org / 10.5962 / bhl. part. 9306","Lopez, E., San Martin, G. & Jimenez, M. (1996) Syllinae (Syllidae, Annelida, Polychaeta) from Chafarinas Islands (Alboran Sea, W. Mediterranean). Miscellania Zoologica, 19 (1), 105 - 118.","San Martin, G. (2003) Annelida Polychaeta II. Syllidae. In: Ramos, M. A. et al. (Eds.), Fauna Iberica. Vol. 21. Museo Nacional de Ciencias Naturales, CSIC, Madrid, pp. 1 - 554.","Musco, L. & Giangrande, A. (2005) Mediterranean Syllidae (Annelida: Polychaeta) revisited: biogeography, diversity and species fidelity to environmental features. Marine Ecology Progress Series. 304: 143 - 153 + 4 pp. Supplementary appendix. https: // doi. org / 10.3354 / meps 304143"]}

Syllis broomensis (Hartmann-Schr��der, 1979) Typosyllis (Langerhansia) broomensis Hartmann-Schr��der, 1979: 88, figs 50���56; 1984: 18; 1989: 23; 1990: 48; 1991: 32. Typosyllis broomensis.��� Licher 1999: 70, fig. 32. Typosyllis (Langerhansia) cervantensis.��� Hartmann-Schr��der 1981, synonymized by Licher 1999: 70. Syllis broomensis.��� ��lvarez-Campos et al. 2015: 302, figs 1, 2. Material examined. Soc/ST���16, MAP 64, SE of Qualansiyah, 12��40.264���N 53��27.204���E, from live colony of Stylophora sp., 6���7 m, coll. M. Apel 08.03.1999, 1 specimen (NHCY 0009). Soc/ST���18, MAP 78A, Qualansiyah Bay, 12��41.026���N 53��28.309���E, 5���6 m, coll. M. Apel 10.3.1999, 1 specimen (SMF 26699). Habitat. On live corals and sand. Mainly in coral rubble, coarse sand and algae (��lvarez-Campos et al. 2015). Distribution. Australia (Queensland; Western Australia; New South Wales); Philippines (Luz��n Island); New Zealand; Caribbean Sea (Cuba); (San Mart��n 1992; ��lvarez-Campos et al. 2015). Type locality. Broome, NW Australia., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2020, New species and records of the genus Syllis Savigny in Lamarck, 1818 (Annelida: Syllidae) from Socotra Archipelago (Indian Ocean), pp. 73-88 in Zootaxa 4742 (1) on page 77, DOI: 10.11646/zootaxa.4742.1.4, http://zenodo.org/record/3674479, {"references":["Hartmann-Schroder, G. (1979) Zur Kenntnis des Eulitorals der australischen Kusten unter besonderer Berucksichtigung der Polychaeten und Ostracoden. Teil 2. Die Polychaeten der tropischen Nordwestkuste Australiens (Zwischen Port Samson im Norden und Port Hedland im Suden). Mitteilungen aus dem Hamburgischen Zoologischen Museum und Institut, 76, 75 - 218.","Licher, F. (1999) Revision der Gattung Typosyllis Langerhans, 1879 (Polychaeta: Syllidae). Morphologie, Taxonomie und Phylogenie. Abhandlungen der Senckenbergischen Naturforschenden Gesellschaft, 551, 1 - 336.","Hartmann-Schroder, G. (1981) Zur Kenntnis des Eulitorals der australischen Kusten unter besonderer Berucksichtigung der Polychaeten und Ostracoden. Teil 6. Die Polychaeten der tropisch-subtropischen Westkuste Australiens (Zwischen Exmouth im Norden und Cervantes im Suden). Mitteilungen aus dem Hamburgischen Zoologischen Museum und Institut, 78, 19 - 96.","Alvarez-Campos, P., San Martin, G. & Hutchings, P. (2015) The genus Syllis Lamarck, 1818 (Annelida, Syllidae) from Australia. Molecular analysis and re-description of some poorly-known species. Zootaxa, 4052 (2), 297 - 331. https: // doi. org / 10.11646 / zootaxa. 4052.3.2","San Martin, G. (1992) Syllis Savigny in Lamarck, 1818 (Polychaeta: Syllidae: Syllinae) from Cuba, the Gulf of Mexico, Florida and North Carolina, with a revision of several species described by Verrill. Bulletin of Marine Science, 51 (2), 169 - 196."]}

Syllis Savigny in Lamarck, 1818 Type species: Syllis monilaris Savigny in Lamarck, 1818, Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2020, New species and records of the genus Syllis Savigny in Lamarck, 1818 (Annelida: Syllidae) from Socotra Archipelago (Indian Ocean), pp. 73-88 in Zootaxa 4742 (1) on page 74, DOI: 10.11646/zootaxa.4742.1.4, http://zenodo.org/record/3674479, {"references":["Lamarck J. B. (1818) Histoire Naturelle des animaux sans vertebres, presentant les caracteres generaux et particuliers de ces animaux, leur distribution, leurs classes, leurs familles, leurs genres, et la citation des principales especes qui s'y rapportent; precedee d'une introduction offrant la determination des caracteres essentiels de l'animal, sa distinction du vegetal et des autres corps naturelles, enfin l'exposition des principes fondamentaux de la zoologie. Deterville, Paris, 5, 612 pp."]}

Syllis hyalina Grube, 1863 Syllis hyalina Grube, 1863: 45, pl. 4, fig. 8; San Mart��n 2003: 426, figs 234, 235. Typosyllis hyalina.��� Licher 1999: 199, pl. 86. Material examined. Rush 009, Samha, 12��10.317���N 53��04.383���E, upper intertidal among algae, 0.5 m, coll. T. Wehe 7.4.2000, 2 specimens (SMF 26709). Soc /ST���16, MAP 60, 12��40.264���N 53��27.204���E, from dead coral (Pocillopora sp.), 6���7 m, coll. M. Apel 8.3.1999, 1 specimen (SMF 26710). Soc /ST-110, Ras Adho (Ras Hammadara), 12��38.534���N 54��15.770���E, 7���12 m, coll. M. Apel 25.03.1999, 1 specimen (NHCY 0016). Habitat. Abundant in littoral areas on hard substrates, also present, but scarcer, in sandy bottoms (San Mart��n 2003). Found in Socotra in mixed coral assemblage: faviids, Astreopora, dead Porites, dead Acropora pallifera (dominant before the 1998 bleaching event). Distribution. Apparently cosmopolitan (San Mart��n 2003). New record for Socotra. Type locality. Losinj (= Lussin Island), Croatia., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2020, New species and records of the genus Syllis Savigny in Lamarck, 1818 (Annelida: Syllidae) from Socotra Archipelago (Indian Ocean), pp. 73-88 in Zootaxa 4742 (1) on page 79, DOI: 10.11646/zootaxa.4742.1.4, http://zenodo.org/record/3674479, {"references":["Grube, A. E. (1863) Beschreibung neuer oder wenig bekannter Anneliden. Archiv fur Naturgeschichte, 29, 37 - 69. https: // doi. org / 10.5962 / bhl. part. 9306","San Martin, G. (2003) Annelida Polychaeta II. Syllidae. In: Ramos, M. A. et al. (Eds.), Fauna Iberica. Vol. 21. Museo Nacional de Ciencias Naturales, CSIC, Madrid, pp. 1 - 554.","Licher, F. (1999) Revision der Gattung Typosyllis Langerhans, 1879 (Polychaeta: Syllidae). Morphologie, Taxonomie und Phylogenie. Abhandlungen der Senckenbergischen Naturforschenden Gesellschaft, 551, 1 - 336."]}

Syllis crassicirrata (Treadwell 1925) Typosyllis crassi-cirrata Treadwell, 1925: 113, figs. 10A���C. Typosyllis crassicirrata.��� Hartman 1966: 198; Licher 1999: 196, fig. 85. Typosyllis (Typosyllis) crassicirrata.��� Hartmann-Schr��der 1979: 90, figs 62���66; 1980: 49; 1981: 25; 1987: 33; 1989: 20; 1992: 53. Syllis crassicirrata.��� ��lvarez-Campos et al. 2015: 306, figs 3, 4; Ba-Akdah et al. 2018: 3, figs 1, 2. Material examined. Soc/ST���95, MAP 95, Shanitan, 12��40.156���N 54��02.850���E, from dead Acropora, 8 m, coll. M. Apel 22.03.1999, 1 specimen (NHCY 0015). Soc /ST���16, MAP 60, 12��40.264���N 53��27.204���E, from dead Pocillopora, 6 ��� 7 m, coll. M. Apel 8.3.1999, 4 specimens (SMF 26703). Soc /ST���67, MAP 137B, Rhiy di-Hamri, 12��40.429���N 54��11.731���E, 7���9 m, coll. M. Apel 19.03.1999, 1 specimen (NHCY 0010). Soc /ST���67, MAP 136, Rhiy di-Hamri, E of Hawlaf, 12��40.429���N 54��11.731���E, 7���9 m, from dead Pocillopora damicornis, coll. M. Apel 19.3.1999, 2 specimens (SMF 26704). Soc /ST���706, Kal Farun, 12��26.049���N 52��08.07���E, 9.5���12.5 m, coll. M. Apel 3.4.2000, 2 specimens (SMF 26706). Soc /ST���37, MAP 154, Shanitan cold store, 12��40.156���N 54��02.850���E, 7���9 m, from dead Acropora sp., coll. M. Apel 21.03.1999, 1 specimen (NHCY 0012). Rush 018, Ras Eriyhan-Quariyeh, 12��38.924���N 54��14.387���E, 10���12 m, coll. T.Wehe 20.4.2000, 1 specimen (SMF 26702). Soc /ST-92, MAP 151, Hawlaf Bay off dune, 12�� 40.519���N 54��4.170���E, from dead colony of Acropora cf. valida, 4���5 m, coll. M. Apel 21.3.1999, 1 specimen (SMF 26705). Soc /ST-18, MAP 77, Qalansiyah Bay, 12�� 41.026���N 53��28.309���E, 5���6 m, coll. M. Apel 10.3.1999, 1 specimen (NHCY 0014). Soc /ST���726, Qataninh Bay, 12��21.293���N 53��32.659���E, under stones and coral rubble, 8���11 m, coll. T. Wehe 9.4.2000, 1 specimen (SMF 26707). Soc /ST���725, Ras Qataninh Bay, dredge, 12��21.789���N 53��31.399���E to 12��21.780���N 53��31.390���E, corals and algae on hard substrate, 18���20 m, coll. T. Wehe 09.04.2000, 1 specimen (NHCY 0013). Soc /ST���18, MAP 78A, Qualansiyah Bay, 12��41.026���N 53��28.309���E, 5���6 m, coll. M. Apel 10.3.1999, 13 specimens (SMF 26701). Habitat. Algae and coarse sediments, pioneer species on artificial panels (Ba-Akdah et al. 2018). Dead corals, rocky substrates. Distribution. Widely distributed in the Pacific and the Indian Ocean: Hawaii, Polynesia, New Zealand, Australia and Red Sea (Ba-Akdah et al. 2018). New record for Socotra. Type localty. Laysan Island, Hawaii., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2020, New species and records of the genus Syllis Savigny in Lamarck, 1818 (Annelida: Syllidae) from Socotra Archipelago (Indian Ocean), pp. 73-88 in Zootaxa 4742 (1) on page 78, DOI: 10.11646/zootaxa.4742.1.4, http://zenodo.org/record/3674479, {"references":["Treadwell, A. L. (1925) Polychaetous Annelids of tropical central Pacific. Bulletin of the Bernice P. Bishop Museum, 27, 113 - 119.","Hartman, O. (1966) Polychaetous Annelids of the Hawaiian Islands. Bernice P. Bishop Museum Occasional Papers, 23, 163 - 252.","Licher, F. (1999) Revision der Gattung Typosyllis Langerhans, 1879 (Polychaeta: Syllidae). Morphologie, Taxonomie und Phylogenie. Abhandlungen der Senckenbergischen Naturforschenden Gesellschaft, 551, 1 - 336.","Hartmann-Schroder, G. (1979) Zur Kenntnis des Eulitorals der australischen Kusten unter besonderer Berucksichtigung der Polychaeten und Ostracoden. Teil 2. Die Polychaeten der tropischen Nordwestkuste Australiens (Zwischen Port Samson im Norden und Port Hedland im Suden). Mitteilungen aus dem Hamburgischen Zoologischen Museum und Institut, 76, 75 - 218.","Alvarez-Campos, P., San Martin, G. & Hutchings, P. (2015) The genus Syllis Lamarck, 1818 (Annelida, Syllidae) from Australia. Molecular analysis and re-description of some poorly-known species. Zootaxa, 4052 (2), 297 - 331. https: // doi. org / 10.11646 / zootaxa. 4052.3.2","Ba-Akdah, M. A., Satheesh, S., Al-Sofyani, A. M. A., Lucas, Y., Alvarez-Campos, P. & San Martin, G. (2018) Taxonomy of some species of the genus Syllis (Annelida: Syllidae: Syllinae) from the Red Sea found among the first colonizers of an artificial substrate. Marine Biological Research, 14 (8), 790 - 805. https: // doi. org / 10.1080 / 17451000.2018.1531133"]}

Syllis alternata Moore, 1908 Syllis alternata Moore, 1908: 323���325, text-fig. a���f, 324; Moore 1909: 321; San Mart��n & Vi��itez 1984: 153, figs 1, 2; ��inar 1999: 246, fig. 4.102; San Mart��n 2003: 354, figs 192, 193. Typosyllis alternata.��� Hartman 1948: 21; Imajima 1966: 273, text-fig. 58; Licher 1999: 253, fig. 106. Syllis (Typosyllis) alternata.��� Gardiner 1976: 141, figs 13b, c; Uebelacker 1984: 30���141, figs. 30���136. Material examined. Soc/ST 706 Kal Farun rock outcrop, 12��26.049���N 52��08.07���E, 9.5���12.5 m, coll. M. Apel, 03.04.2000, 1 specimen (SMF 26697). Habitat. In coralligenous concretions, algae, M��erl, Posidonia rhizomes, detritic bottoms, vermetid reefs, calcareous algae (San Mart��n 2003). Distribution. Northeastern Pacific Ocean, from Alaska to California. Chukchi Sea. Japan. Caribbean Sea. Gulf of M��xico. Northeastern Atlantic. Mediterranean Sea. Indian Ocean. Apparently cosmopolitan, mainly in the northern hemisphere, but some of these records are probably the result of misidentifications (Read & Fauchald 2019), and S. alternata may be a complex of species. New record for Socotra. Type locality. Vincinity of Naha Bay, Behm Canal, SO-Alaska., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2020, New species and records of the genus Syllis Savigny in Lamarck, 1818 (Annelida: Syllidae) from Socotra Archipelago (Indian Ocean), pp. 73-88 in Zootaxa 4742 (1) on page 75, DOI: 10.11646/zootaxa.4742.1.4, http://zenodo.org/record/3674479, {"references":["Moore, J. P. (1908) Some Polychaetous Annelids of the Northern Pacific Coast of North America. Proceedings of the Academy of Natural Sciences of Philadelphia, 60, 321 - 364.","Moore, J. P. (1909) The polychaetous annelids dredged by the Albatross \" off the coast of California in 1904. I. Syllidae, Sphaerodoridae, Hesionidae, Phyllodocidae. Proceedings of the Academy of Natural Sciences of Philadelphia, 61, 321 - 351. https: // doi. org / 10.5962 / bhl. title. 12425","San Martin, G. & Vieitez, J. M. (1984) Anelidos Poliquetos de los rizomas de Posidonia oceanica en las costas de Cabo de Palos (Murcia, Espana). In: Boudouresque, C. F., Jeudy de Grissac, A. & Oliver, J. (Eds.), International Workshop on Posidonia oceanica beds. G. I. S. Posidonie Publication 1. G. I. S. Posidonie Publ., Marseille, pp. 149 - 157.","Cinar, M. E. (1999) Turkiye'nin Ege Denizi sahillerinde dadylym gosteren syllidae (Polychaeta-Annelida) turlerinin taksonomisi ve ekolojisi. PhD Thesis, Ege University, Izmir, 443 S.","San Martin, G. (2003) Annelida Polychaeta II. Syllidae. In: Ramos, M. A. et al. (Eds.), Fauna Iberica. Vol. 21. Museo Nacional de Ciencias Naturales, CSIC, Madrid, pp. 1 - 554.","Hartman, O. (1948) The polychaetous annelids of Alaska. Pacific Science, 2 (1), 1 - 58.","Imajima, M. (1966) The Syllidae (Polychaetous Annelids) from Japan (V). Syllinae (2). Publications of the Seto Marine Biological Laboratory, 14 (4), 253 - 294. https: // doi. org / 10.5134 / 175446","Licher, F. (1999) Revision der Gattung Typosyllis Langerhans, 1879 (Polychaeta: Syllidae). Morphologie, Taxonomie und Phylogenie. Abhandlungen der Senckenbergischen Naturforschenden Gesellschaft, 551, 1 - 336.","Gardiner, S. L. (1976) Errant polychaete annelids from North Carolina. Journal of the Elisha Mitchell Scientific Society, 91 (3), 77 - 220.","Uebelacker, J. M. (1984) Family Syllidae Grube, 1850. In: Uebelacker, J. M. & Johnson, P. G. (Eds.), Taxonomic guide to the polychaetes of the northern Gulf of Mexico. Vol. IV. Mobile, Barry A. Vittor and Associates, Alabama, pp. 1 - 151.","Read, G. & Fauchald, K. (Eds.) (2019) World Polychaeta database. Syllis Lamarck, 1818. World Register of Marine Species. Available from: http: // www. marinespecies. org / aphia. php? p = taxdetails & id = 129680 (accessed 24 July 2019)"]}

Syllis bouvieri Gravier, 1900 Figure 1 Syllis bouvieri Gravier, 1900: 163, pl. IX, fig. 40. Non Syllis bouvieri San Mart��n 1984: 374, pls. 96, 97. Material examined. Soc/ST���18, MAP 78A, Qualansiyah Bay, 12��41.026���N 53��28.309���E, 5���6 m, coll. M. Apel 10.3.1999, 1 specimen (NHCY 0008). Soc/ST���92, MAP 151, Hawlaf Bay (off dune), 12��40.519���N 54��04.170���E, from Acropora cf. valida, 4���5 m, coll. M. Apel 21.3.1999, 1 specimen (SMF 26698). Additional material examined. Holotype ( MNHN 0146). Djibouti, Gulf of Aden. Description. Body long and slender, without colour pattern, 10.5 mm long, 0.8 mm wide, with approximately 64���67 chaetigers. Prostomium semicircular; 4 small reddish eyes in open trapezoidal arrangement. Palps robust, similar in length to prostomium. Median antenna arising between anterior eyes, with 38���40 articles, longer than combined length of prostomium and palps. Lateral antennae shorter than median one, with 20���22 articles. Peristomium dorsally similar in length to subsequent segments (Fig. 1A); dorsal tentacular cirri with about 30���33 articles, slightly longer than median antenna; ventral tentacular cirri with about 15���16 articles, slightly shorter than lateral antennae. Dorsal parapodial cirri long, pointed distally, with well-marked articles; first pair with about 41���44 articles, longer than body width. Midbody dorsal parapodial cirri with a slight alternation in length, about 30���26 articles, slightly thicker than anterior ones. Parapodia conical, distally slightly bilobed; ventral parapodial cirri digitiform, shorter than parapodial lobes. Compound chaetae heterogomph, with one or two dorsalmost chaetae having slender, elongated blades with both teeth similar and usually with rounded space in between, and moderate spines on margin, lightly curved upward (Fig. 1B, D, F); remaining falcigers distinctly shorter, nine on anterior parapodia, progressively diminishing to seven on midbody and six on posterior parapodia, blades bidentate with similar teeth, and moderate to short curved spines on margin (Fig. 1B, D, F). Blades of falcigers with dorsoventral gradation in length; slender, dorsalmost elongated blades 36 ��m long on anterior parapodia, 47 ��m on midbody, 42 ��m long on posterior parapodia; remaining falcigers 30���23 ��m long on anterior parapodia, 26���25 ��m on midbody, 26���17 ��m long on posterior parapodia. Anterior parapodia with three slender aciculae each, distally rounded (Fig. 1C), reducing to two in midbody parapodia, one subdistally slightly inflated with small oblique tip (Fig. 1E); posterior parapodia with one acicula each, distally bent at almost right angle, with acuminated tip (Fig. 1G). Dorsal simple capillary chaetae on posterior parapodia, thin, acute, apparently unidentate (Fig. 1H). Ventral simple capillary chaetae bidentate with some short spines on inner margin (Fig. 1I). Pharynx long, through about 8���9 segments; pharyngeal tooth elongated, conical, acute, on anterior margin of pharynx (Fig. 1A). Proventricle through six segments, with about 30 muscle cell rows., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2020, New species and records of the genus Syllis Savigny in Lamarck, 1818 (Annelida: Syllidae) from Socotra Archipelago (Indian Ocean), pp. 73-88 in Zootaxa 4742 (1) on page 75, DOI: 10.11646/zootaxa.4742.1.4, http://zenodo.org/record/3674479, {"references":["Gravier, C. (1900) Contribution a l'etude des annelides polychetes de la Mer Rouge. Premiere partie. Nouvelles Archives du Museum d'Histoire Naturelle, Paris, 2, 137 - 282. https: // doi. org / 10.5962 / bhl. part. 9306"]}

Syllis schulzi (Hartmann-Schr��der, 1960) Typosyllis schulzi Hartmann-Schr��der, 1960: 80, pl. 2, fig. 34, pl. 5, figs 35���37; Licher 1999: 140. Syllis (Typosyllis) schulzi.��� Ben-Eliahu 1977: 21, figs. 6a���i. Syllis schulzi.��� San Mart��n 2003: 364, fig. 198; Ba-Akdah et al. 2018: 8, fig. 5. Material examined. Soc/ST���16, MAP 60, 12��40.264���N 53��27.204���E, dead coral (Pocillopora sp.), 6���7 m, coll. M. Apel 8.3.1999, 2 specimens (SMF 26712). Soc/ST���16, MAP 61, SE of Qualansiyah, 12��40.264���N 53��27.204���E, dead coral, 5���6 m, coll. M. Apel 08.03.1999, 1 specimen (NHCY 0017). Habitat. Coral rubble, algae, vermetid reefs; pioneer on artificial panels. Intertidal and shallow depths. Distribution. Red Sea and Southern Mediterranean (Ba���Akdah et al. 2018). New record for Socotra. Type locality. Ghardaqa, Red Sea., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2020, New species and records of the genus Syllis Savigny in Lamarck, 1818 (Annelida: Syllidae) from Socotra Archipelago (Indian Ocean), pp. 73-88 in Zootaxa 4742 (1) on page 85, DOI: 10.11646/zootaxa.4742.1.4, http://zenodo.org/record/3674479, {"references":["Hartmann-Schroder, G. (1960) Polychaeten aus dem Roten Meer. Kieler Meeresforschungen, 16, 69 - 125.","Licher, F. (1999) Revision der Gattung Typosyllis Langerhans, 1879 (Polychaeta: Syllidae). Morphologie, Taxonomie und Phylogenie. Abhandlungen der Senckenbergischen Naturforschenden Gesellschaft, 551, 1 - 336.","Ben-Eliahu, N. M. (1977) Polychaete cryptofauna from rims of similar intertidal vermetid reefs on the Mediterranean coast of Israel and in the Gulf of Eilat: Syllinae and Eusyllinae (Polychaeta Errantia: Syllidae). Israel Journal of Zoology, 26, 1 - 58.","San Martin, G. (2003) Annelida Polychaeta II. Syllidae. In: Ramos, M. A. et al. (Eds.), Fauna Iberica. Vol. 21. Museo Nacional de Ciencias Naturales, CSIC, Madrid, pp. 1 - 554.","Ba-Akdah, M. A., Satheesh, S., Al-Sofyani, A. M. A., Lucas, Y., Alvarez-Campos, P. & San Martin, G. (2018) Taxonomy of some species of the genus Syllis (Annelida: Syllidae: Syllinae) from the Red Sea found among the first colonizers of an artificial substrate. Marine Biological Research, 14 (8), 790 - 805. https: // doi. org / 10.1080 / 17451000.2018.1531133"]}

Syllis gerlachi (Hartmann-Schr��der, 1960) Typosyllis gerlachi Hartmann-Schr��der, 1960: 81, pl.6, figs 43���44, pl. 7, fig. 42. Syllis (Typosyllis) gerlachi.��� Ben���Eliahu 1977: 19, fig. 5. Syllis gerlachi.��� Ba-Akdah et al. 2018: 5, fig. 3. Non Typosyllis gerlachi.��� Campoy 1982: 410, pl. 45. Non Syllis (Typosyllis) gerlachi. ��� Uebelacker 1984: 30���145, fig. 142. Non Typosyllis gerlachi. ��� Licher 1999: 127, pl. 57. Non Syllis gerlachi. ��� San Mart��n 2003: 376, figs 205, 206. Material examined. Soc/ST���95, MAP 95, Shanitan, 12��40.156���N 54��02.850���E, from dead Acropora cf. valida, 8 m, coll. M. Apel 22.03.1999, 1 specimen (SMF 26708). Remarks. Ba-Akdah et al. (2018) redescribed S. gerlachi and provided an overview about the misidentifications of this species in the literature. Habitat. On dead corals. Pioneer on artificial panels (Ba-Akdah et al. 2018). Distribution. Red Sea (Ba-Akdah et al. 2018). First record for Socotra. Type locality. Sarso, Red Sea., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2020, New species and records of the genus Syllis Savigny in Lamarck, 1818 (Annelida: Syllidae) from Socotra Archipelago (Indian Ocean), pp. 73-88 in Zootaxa 4742 (1) on pages 78-79, DOI: 10.11646/zootaxa.4742.1.4, http://zenodo.org/record/3674479, {"references":["Hartmann-Schroder, G. (1960) Polychaeten aus dem Roten Meer. Kieler Meeresforschungen, 16, 69 - 125.","Ben-Eliahu, N. M. (1977) Polychaete cryptofauna from rims of similar intertidal vermetid reefs on the Mediterranean coast of Israel and in the Gulf of Eilat: Syllinae and Eusyllinae (Polychaeta Errantia: Syllidae). Israel Journal of Zoology, 26, 1 - 58.","Ba-Akdah, M. A., Satheesh, S., Al-Sofyani, A. M. A., Lucas, Y., Alvarez-Campos, P. & San Martin, G. (2018) Taxonomy of some species of the genus Syllis (Annelida: Syllidae: Syllinae) from the Red Sea found among the first colonizers of an artificial substrate. Marine Biological Research, 14 (8), 790 - 805. https: // doi. org / 10.1080 / 17451000.2018.1531133","Campoy, A. (1982) Fauna de Espana. Fauna de Anelidos Poliquetos de la Peninsula Iberica. Serie Biologica. EUNSA (Ediciones de la Universidad de Navarra, S. A.), Pamplona, 781 pp.","Uebelacker, J. M. (1984) Family Syllidae Grube, 1850. In: Uebelacker, J. M. & Johnson, P. G. (Eds.), Taxonomic guide to the polychaetes of the northern Gulf of Mexico. Vol. IV. Mobile, Barry A. Vittor and Associates, Alabama, pp. 1 - 151.","Licher, F. (1999) Revision der Gattung Typosyllis Langerhans, 1879 (Polychaeta: Syllidae). Morphologie, Taxonomie und Phylogenie. Abhandlungen der Senckenbergischen Naturforschenden Gesellschaft, 551, 1 - 336.","San Martin, G. (2003) Annelida Polychaeta II. Syllidae. In: Ramos, M. A. et al. (Eds.), Fauna Iberica. Vol. 21. Museo Nacional de Ciencias Naturales, CSIC, Madrid, pp. 1 - 554."]}

Syllis qamhiyn n.sp. Figures 2���6 urn:lsid:zoobank.org:act: A270D267-0901-4185-80E4-E6D0AAC48A49 Material examined. Holotype (SMF 26713) Soc /ST���726, Ras Qataninh Bay, 12��21.293���N 53��32.659���E, under stones and coral rubble, 8���10 m, coll. T. Wehe 9.4.2000. 1 paratype, same collection data (NHCY 0018); 1 paratype prepared for SEM, Soc/ST���725, Ras Qataninh Bay, dredge, 12��21.789���N 53��31.399���E to 12��21.780���N 53��31.390���E, 18���20 m, coll. T. Wehe 09.04.2000, (SMF 26714, SEM-stub 1311). Diagnosis. Conspicuously thick and short dorsal cirri filled with gelatinous substance; reduced number of compound chaetae from midbody to posterior parapodia, with enlarged shafts and short blades, which become almost unidentate; blades not fused to shafts. Description. Holotype complete specimen, 17.5 mm long, 0.69 mm wide, with 151 chaetigers (Fig. 2A). One incomplete paratype with 134 chaetigers, and other complete, Paratype (SMF 26714), 18.5 mm long, 0,5 mm wide, with 160 chaetigers (Fig. 4B). Body long and slender, filiform, without colour pattern (Figs 2A, B, C; 4B). Prostomium semicircular to oval (Figs 2A; 5A); four small eyes in trapezoidal arrangement. Palps similar in length to prostomium. Median antenna arising between anterior eyes, with 12���13 articles, shorter than combined length of prostomium and palps. Lateral antennae same length as median antenna, with 13 articles each (Fig. 2A). Peristomium dorsally shorter than subsequent segments (Figs. 2A; 5B). Dorsal tentacular cirri about 15���21 articles each; ventral tentacular cirri about 13���14 articles each. Dorsal parapodial cirri relatively thin on anterior segments, alternating relatively long (0.3 mm) and short (0.2 mm); longer cirri similar in length to body width at corresponding chaetiger, with about 17���19 articles, shorter ones about 7���11 articles each (Fig. 2A); from midbody posteriorwards, dorsal cirri shorter than body width, each cirrus thicker in midlength, with about eight well-marked articles, with acute article distally (Fig. 2 A���D); most articles of these dorsal cirri filled with gelatinous substance (Fig. 2D), articles covered by small pores (Fig. 5F). Ventral cirri oval, shorter than parapodial lobes (Figs 2D; 6D). Ventral area of parapodia with almost circular area of pores (Fig. 6 C���E) and internal gland (Fig. 2D). Compound chaetae as heterogomph falcigers; anterior parapodia with about 10 falcigers each; falcigers with slender bidentate blades, proximal tooth distinctly shorter than distal one, and short spines on margin; blades with dorsoventral gradation in length, 42���20 ��m long (Figs 3A; 5C, D). Number of chaetae per parapodium progressively diminishing posteriorly, 4���5 in midbody (Figs 3C; 5E, G, H) and 3���5 on mid-posterior and posterior parapodia (Figs 3E; 6 A���B), shafts becoming larger and blades shorter and minutely bidentate, with proximal tooth much smaller than distal one (Fig. 3E). Midbody falcigers with blades 20���19 ��m long, posterior body falcigers with blades similar, about 19 ��m long. Dorsal and ventral simple chaetae not seen. Anterior parapodia with five slender aciculae each, distally rounded (Fig. 3B), three in midbody parapodia (Fig. 3D); posterior parapodia with two distally oblique aciculae each (Fig. 3F). Pharynx long, extending through about 13 segments (Figs 2A; 4B); pharyngeal tooth elongated, conical, acute, on anterior margin of pharynx (Figs 2A, 4A). Proventricle shorter than pharynx, through 9���10 segments (Fig. 2A), with about 48���50 muscle cell bands. Pygidium small, with two anal cirri, with 7���8 articles each (Fig. 6F). Etymology. The name of the species refers to Dendrosicyos socotrana, the only species of Cucurbitaceae growing into tree form and original from Socotra Island. Its trunk resembles the shape of midbody cirri of S. qamhiyn n.sp. In soqotri language it is named qamhiyn. Remarks. Syllis qamhiyn n.sp. is characterized by having short, thick, distally acute dorsal cirri on midbody and posterior parapodia, and reduced number of falcigers in these parapodia, with enlarged shafts and short, almost unidentate blades, not fused to shafts. Syllis qamhiyn n.sp. belongs to the same group of species of Syllis armillaris (O. F. M��ller, 1771) and related species, the latter considered cosmopolitan but likely a species complex. The mid- and posterior body falcigers of Syllis armillaris also have almost unidentate blades, but they are not so short and the shafts are not as enlarged as in Syllis qamhiyn n.sp. (San Mart��n 2003); furthermore, the mid- and posterior body dorsal cirri of Syllis armillaris are enlarged, but not so much as in Syllis qamhiyn n.sp. Similar differences are between Syllis qamhiyn n.sp. and S. pseudoarmillaris Nogueira & San Mart��n, 2002 from Brazil (Nogueira & San Mart��n 2002); S. pseudoarmillaris has fewer number of articles on midbody dorsal cirri and the compound chaetae of these parapodia are clearly bidentate, with not enlarged shafts; furthermore, the pharynx and proventricle are longer in S. qamhiyn n.sp. Syllis gracilis Grube, 1840, also considered a cosmopolitan species, and S. picta (Kinberg, 1886), from the Indo-Pacific (including the Red Sea), have similar bodies, with enlarged mid- and posterior body dorsal cirri, but in these species at least one of the compound chaetae on these parapodia have fused blade and shaft (San Mart��n 2003; ��lvarez-Campos et al. 2015; 2017). Habitat. Under stones and coral rubble from 8��� 20 m. Distribution. Only known from Socotra Archipelago. Type locality. Ras Qataninh Bay, Socotra Island., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2020, New species and records of the genus Syllis Savigny in Lamarck, 1818 (Annelida: Syllidae) from Socotra Archipelago (Indian Ocean), pp. 73-88 in Zootaxa 4742 (1) on pages 79-85, DOI: 10.11646/zootaxa.4742.1.4, http://zenodo.org/record/3674479, {"references":["Muller, O. F. (1771) Von den Nereiden. Von Wurmern des sussen und salzigen Wassers. Heineck und Faber, Kopenhagen, 98 pp. [pp. 103 - 200] https: // doi. org / 10.5962 / bhl. title. 14428","San Martin, G. (2003) Annelida Polychaeta II. Syllidae. In: Ramos, M. A. et al. (Eds.), Fauna Iberica. Vol. 21. Museo Nacional de Ciencias Naturales, CSIC, Madrid, pp. 1 - 554.","Nogueira, J. M. & San Martin, G. (2002) Species of Syllis Lamarck, 1818 (Polychaeta: Syllidae) living in corals in the state of Sao Paulo, southeastern Brazil. Beaufortia, 52 (7), 57 - 93.","Grube, E. (1840) Actinien, Echinodermen und Wurmer des Adriatischen- und Mittelmeers nach eigenen Sammlungen beschrieben. Verlag J. H. Bon Konigsberg, 92 pp. https: // doi. org / 10.5962 / bhl. title. 10133","Alvarez-Campos, P., San Martin, G. & Hutchings, P. (2015) The genus Syllis Lamarck, 1818 (Annelida, Syllidae) from Australia. Molecular analysis and re-description of some poorly-known species. Zootaxa, 4052 (2), 297 - 331. https: // doi. org / 10.11646 / zootaxa. 4052.3.2"]}

Syllis lutea (Hartmann-Schr��der, 1960) Typosyllis lutea Hartmann-Schr��der, 1960: 81, pl. 2, fig. 38, pl. 5, figs 39���41; Licher 1999: 177, fig. 79. Typosyllis (Typosyllis) lutea. ��� Hartmann-Schr��der 1979: 89; 1981: 27; 1982: 59; 1991: 29. Syllis (Typosyllis) lutea. ��� Ben-Eliahu 1977: 40. Syllis lutea. ��� Nogueira & San Mart��n 2002: 75, figs 13, 14; San Mart��n et al. 2017: 216, fig. 9. Typosyllis regulata Imajima, 1966: 289, text-fig. 64 a���n. Material examined. Soc/ST���18, MAP 78A, Qualansiyah Bay, 12��41.026���N 53��28.309���E, from dead branched corals, 5���6 m, coll. M. Apel 10.3.1999, 1 specimen (SMF 26711). Habitat. Algae, seaweeds, dead corals, coarse sand, mud. Intertidal to sublittoral (San Mart��n et al. 2017). Distribution. Circumtropical. Red Sea; Japan; Brazil; Cuba; Australia (Queensland; Western Australia) (San Mart��n et al. 2017). New record for Socotra. Type locality. Sarso, Red Sea., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2020, New species and records of the genus Syllis Savigny in Lamarck, 1818 (Annelida: Syllidae) from Socotra Archipelago (Indian Ocean), pp. 73-88 in Zootaxa 4742 (1) on page 79, DOI: 10.11646/zootaxa.4742.1.4, http://zenodo.org/record/3674479, {"references":["Hartmann-Schroder, G. (1960) Polychaeten aus dem Roten Meer. Kieler Meeresforschungen, 16, 69 - 125.","Licher, F. (1999) Revision der Gattung Typosyllis Langerhans, 1879 (Polychaeta: Syllidae). Morphologie, Taxonomie und Phylogenie. Abhandlungen der Senckenbergischen Naturforschenden Gesellschaft, 551, 1 - 336.","Hartmann-Schroder, G. (1979) Zur Kenntnis des Eulitorals der australischen Kusten unter besonderer Berucksichtigung der Polychaeten und Ostracoden. Teil 2. Die Polychaeten der tropischen Nordwestkuste Australiens (Zwischen Port Samson im Norden und Port Hedland im Suden). Mitteilungen aus dem Hamburgischen Zoologischen Museum und Institut, 76, 75 - 218.","Hartmann-Schroder, G. (1981) Zur Kenntnis des Eulitorals der australischen Kusten unter besonderer Berucksichtigung der Polychaeten und Ostracoden. Teil 6. Die Polychaeten der tropisch-subtropischen Westkuste Australiens (Zwischen Exmouth im Norden und Cervantes im Suden). Mitteilungen aus dem Hamburgischen Zoologischen Museum und Institut, 78, 19 - 96.","Hartmann-Schroder, G. (1982) Zur Kenntnis des Eulitorals der australischen Kusten unter besonderer Berucksichtigung der Polychaeten und Ostracoden. Teil 8. Die Polychaeten der subtropischen-antiborealen Westkuste Australiens (Zwischen Cervantes im Norden und Cape Naturaliste im Suden). Mitteilungen aus dem Hamburgischen Zoologischen Museum und Institut, 79, 51 - 118.","Hartmann-Schroder, G. (1991) Zur Kenntnis des Eulitorals der australischen Kusten unter besonderer Berucksichtigung der Polychaeten und Ostracoden. Teil 16. Die Polychaeten der subtropisch-tropischen bis tropischen Ostkuste Australiens zwischen Maclean (New South Wales) und Gladstone (Queensland) sowie von Heron Island (Grosses Barriere-Riff). Mitteilungen aus dem Hamburgischen Zoologischen Museum und Institut, 88, 17 - 71.","Ben-Eliahu, N. M. (1977) Polychaete cryptofauna from rims of similar intertidal vermetid reefs on the Mediterranean coast of Israel and in the Gulf of Eilat: Syllinae and Eusyllinae (Polychaeta Errantia: Syllidae). Israel Journal of Zoology, 26, 1 - 58.","Nogueira, J. M. & San Martin, G. (2002) Species of Syllis Lamarck, 1818 (Polychaeta: Syllidae) living in corals in the state of Sao Paulo, southeastern Brazil. Beaufortia, 52 (7), 57 - 93.","San Martin, G., Alvarez-Campos, P. & Hutchings, P. (2017) The genus Syllis Savigny in Lamarck, 1818 (Annelida: Syllidae: Syllinae) from Australia (second part): four new species and re-description of twelve previously described species. Zootaxa, 4237 (2), 201 - 243. https: // doi. org / 10.11646 / zootaxa. 4237.2.1","Imajima, M. (1966) The Syllidae (Polychaetous Annelids) from Japan (V). Syllinae (2). Publications of the Seto Marine Biological Laboratory, 14 (4), 253 - 294. https: // doi. org / 10.5134 / 175446"]}

Eusyllis assimilis Marenzeller, 1875 Eusyllis assimilis Marenzeller, 1875: 158, pl. 3, fig. 2.��� Fauvel, 1923: 294, fig. 112 a���g. San Mart��n, 2003: 114, figs. 52, 53. Eudontosyllis aciculata Knox, 1960: 105, figs. 113���117. Material examined. Socotra, N coast, Southeast of Qualansiyah, 12��40.264���N 53��27.204E, dead coral, 5���6 m, 08.03.1999, 1 specimen (NHCY 007). Socotra, N coast, Shanitan, 600 m off cold store, 12��40.156N 54��02.850E, 8 m, dead Acropora, 22.03.1999, 2 specimens and additional broken posterior piece (SMF 24993). Habitat. Occurring on different kind of substrates (algae, dead corals, sand), from 5 m as in Socotra samples, to more than 500 m depth. (San Mart��n & Hutchings, 2006). Distribution. North Atlantic, Mediterranean Sea, North Pacific, New Zealand, Australia (Western Australia, South Australia, New South Wales) and Arabian Sea. (North West Indian Ocean) (San Mart��n & Hutchings 2006)., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2019, A new species and nine new records of Syllidae (Annelida) from the Socotra Archipelago (Indian Ocean), pp. 235-258 in Zootaxa 4651 (2) on page 251, DOI: 10.11646/zootaxa.4651.2.2, http://zenodo.org/record/3363175, {"references":["Marenzeller, E. (1875) Zur Kenntnis der adriatischen Anneliden. Zweiter Beitrag. (Polynoinen, Hesioneen, Syllideen). Sitzungsberichte der Akademie der Wissenschaften in Wien. Mathematisch-Naturwissenschaftliche Klasse. Abteilung I: Mineralogie, Biologie, Erdkunde, 72, 129 - 171.","Fauvel, P. (1923) Polychetes Errantes. Faune France, 5, 1 - 488.","San Martin, G. (2003) Annelida, Polychaeta II. Syllidae. In: Ramos, M. A., Alba, J., Belles, X., Gosalbez, J., Guerra, A., Macpherson, E., Martin, F., Serrano, J. & Templado, J. (Eds.), Fauna Iberica. Vol. 21. Museo Nacional de Ciencias Naturales, CSIC, Madrid, pp. 1 - 554.","Knox, G. A. (1960) Biological results of the Chatman Islands 1954 Expedition. Part 3. Polychaeta Errantia. Memoirs of the New Zealand Oceanography Institute, 6, 77 - 143.","San Martin, G. & Hutchings, P. (2006) Eusyllinae (Polychaeta, Syllidae) from Australia with the description of a new genus and fifteen new species. Records of the Australian Museum, 58, 257 - 370. https: // doi. org / 10.3853 / j. 0067 - 1975.58.2006.1466"]}

Eusyllis Malmgren, 1867 Eusyllis Malmgren, 1867: 40. Eudontosyllis Knox, 1960: 105. Type species: Eusyllis blomstrandi Malmgren, 1867., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2019, A new species and nine new records of Syllidae (Annelida) from the Socotra Archipelago (Indian Ocean), pp. 235-258 in Zootaxa 4651 (2) on page 251, DOI: 10.11646/zootaxa.4651.2.2, http://zenodo.org/record/3363175, {"references":["Malmgren, A. J. (1867) Annulata Polychaeta Spetsbergiae Groenlandiae, Islandiae et Scandinaviae hactenus cognita. Ofversigt af Kongliga Vetenskaps-Akademiens Forhandlingar, 24, 1 - 127. https: // doi. org / 10.5962 / bhl. title. 13358","Knox, G. A. (1960) Biological results of the Chatman Islands 1954 Expedition. Part 3. Polychaeta Errantia. Memoirs of the New Zealand Oceanography Institute, 6, 77 - 143."]}

Megasyllis San Mart��n, Hutchings & Aguado, 2008 Type species: Syllis corruscans Haswell, 1886., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2019, A new species and nine new records of Syllidae (Annelida) from the Socotra Archipelago (Indian Ocean), pp. 235-258 in Zootaxa 4651 (2) on page 237, DOI: 10.11646/zootaxa.4651.2.2, http://zenodo.org/record/3363175, {"references":["San Martin, G., Hutchings, P. & Aguado, M. T. (2008) Syllinae (Polychaeta, Syllidae) from Australia. Part. 2. Genera Inermosyllis, Megasyllis n. gen., Opisthosyllis, and Trypanosyllis. Zootaxa, 1840 (1), 1 - 53. https: // doi. org / 10.11646 / zootaxa. 1840.1.1","Haswell, W. A. (1886) Observations on some Australian Polychaeta. Proceedings of the Linnean Society of New South Wales, 10, 733 - 756. https: // doi. org / 10.5962 / bhl. part. 17962"]}

Odontosyllis Clapar��de, 1863 Odontosyllis Clapar��de, 1863: 47. San Mart��n, 2003: 101.��� San Mart��n & Hutchings, 2006: 257���370.��� Verdes et al. 2011: 29. Eurymedusa Kinberg, 1865: 61. Parautolytus Ehlers, 1900: 213. Alluaudella Gravier, 1905: 372. Atelesyllis Pruvot, 1930: 39. Pharyngeovalvata Day, 1951: 26. Odontoautolytus Hartmann-Schr��der, 1979: 112. Synpalposyllis Hartmann-Schr��der, 1983: 132. Umbellisyllis Sars, 1869: 254. Type species: Syllis fulgurans Audouin & Milne Edwards, 1833, designated by Hartman, 1959., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2019, A new species and nine new records of Syllidae (Annelida) from the Socotra Archipelago (Indian Ocean), pp. 235-258 in Zootaxa 4651 (2) on page 250, DOI: 10.11646/zootaxa.4651.2.2, http://zenodo.org/record/3363175, {"references":["Claparede, E. (1863) Beobachtungen uber Anatomie und Entwicklungsgeschichte wirbelloser Thiere an der Kuste von Nor- mandie angestellt. Wilhelm Engelmann, Leipzig, 120 pp. https: // doi. org / 10.5962 / bhl. title. 10030","San Martin, G. (2003) Annelida, Polychaeta II. Syllidae. In: Ramos, M. A., Alba, J., Belles, X., Gosalbez, J., Guerra, A., Macpherson, E., Martin, F., Serrano, J. & Templado, J. (Eds.), Fauna Iberica. Vol. 21. Museo Nacional de Ciencias Naturales, CSIC, Madrid, pp. 1 - 554.","San Martin, G. & Hutchings, P. (2006) Eusyllinae (Polychaeta, Syllidae) from Australia with the description of a new genus and fifteen new species. Records of the Australian Museum, 58, 257 - 370. https: // doi. org / 10.3853 / j. 0067 - 1975.58.2006.1466","Verdes, A. & Pleijel, F. & Aguado, M. T. (2011) A new species of Odontosyllis Claparede, 1863 (Annelida, Syllidae) with re-descriptions of O. liniata Hartmann-Schroder, 1962 and O. gymnocephala Hartmann-Schroder, 1965. Zootaxa, 3095, 27 - 38.","Kinberg, J. G. H. (1865) Annulata nova. Ofversigt af Kongliga Svenska Vetenskaps-Akademiens Forhandlingar, 22, 239 - 258.","Ehlers, E. (1900) Magellanische Anneliden gesammelt wahrend der Schwedischen Expedition nach den Magellanslandern. Festschrift zur Feier des Hundertfunfzigjahrigen Bestehens der Koniglichen Gesellschaft der Wissenschaften zu Gottingen, 1900, 206 - 223.","Gravier, C. (1905) Sur un nouveau Syllidien, Alluaudella nov. gen., madagascariensis nov. sp. Comptes Rendues International Congres de Zoologie de Berne, 6, 372 - 376.","Pruvot, G. (1930) Annelides Polychetes de Nouvelle-Caledonie recueillies par M. Francois, avec une introduction de Pierre Fauvel. Archives de Zoologie Experimentale et Generale, 70, 1 - 94.","Day, J. H. (1951) The polychaete fauna of South Africa. Part 1: The intertidal and estuarine Polychaeta of Natal and Mocambique. Annals of Natal Museum, 12, 1 - 67.","Hartmann-Schroder, G. (1979) Zur Kenntnis des Eulitorals der australischen Kusten unter besonderer Berucksichtigung der Polychaeten und Ostracoden. Teil 2. Die Polychaeten der tropischen Nordwestkuste Australiens (Zwischen Port Samson im Norden und Port Hedland in Suden). Mitteilungen aus dem Hamburgischen Zoologischen Museum und Institut, 76, 75 - 218.","Hartmann-Schroder, G. (1983) Zur Kenntnis des Eulitorals der australischen Kusten unter besonderer Berucksichtigung der Polychaeten und Ostracoden. Teil 9. Die Polychaeten der antiborealen Sudwestkuste Australiens (zwischen Dunsborough im Norden und Denmark im Suden). Mitteilungen aus dem Hamburgischen Zoologischen Museum und Institut, 80, 123 - 167.","Sars, M. (1869) Fortsatte Bemaerkninger over det dyriske Livs Udbredning i Havets Dybder Forhandlingar fra Videnskabs- Selskabet i Kristiania, 1869, 246 - 275. https: // doi. org / 10.5962 / bhl. title. 51281","Audouin, J. V. & Milne Edwards, H. (1833) Classification des Annelides et description de celles qui habitent les cotes de la France. Annales des Sciences Naturelles, Paris, 1, 29, 195 - 269. https: // doi. org / 10.5962 / bhl. part. 8010","Hartman, O. (1959) Catalogue of the polychaetous annelids of the world. Parts I, II (1959), and Supplement (1965). Allan Hancock Foundation Publications, Occasional Papers, 23, 1 - 828."]}

Megasyllis heterosetosa (Hartmann-Schröder, 1991) Figures 1–3 Typosyllis (Typosyllis) heterosetosa Hartmann-Schröder, 1991: 30, figs. 30–35. “ Typosyllis ” heterosetosa (sic) Licher 1999: 298, fig. 115. Megasyllis heterosetosa San Martín et al. 2008: 8–11, figs. 9, 10. Material examined. Socotra, N coast, 12º36.369N 54º19.751E, intertidal, 09.02.1999, 1 specimen (including 4 permanent slides of parapodia) (SMF 24978). Description. Specimen difficult to examine, strongly coiled, hardened and fragile. Body long, broad and strongly built, cylindrical (Fig. 1A), ventrally flattened; about 27 mm long (including stolon), 1.3 mm wide, about 75 segments plus incomplete stolon; yellowish, opaque in alcohol. Prostomium small, short, oval to bilobed, strongly contracted and difficult to observe. Four small orange eyes in trapezoidal arrangement. Antennae shorter than combined length of prostomium and palps; lateral antennae inserted on anterior margin of prostomium, slightly shorter than median antenna; median antenna inserted near posterior margin. Palps large, broad, divergent, basally fused, similar in length to prostomium, ventrally orientated. Peristomium similar in length to subsequent segments; most anterior segments short, sub-divided into 2–3 rings. Median segments inflated, with segmental rings slightly marked (Fig. 1A). Tentacular cirri longer than antennae, dorsal ones slightly shorter than half peristomial width and longer than ventral ones. Antennae, tentacular and dorsal cirri appearing smooth, unarticulated under low magnification; under high magnification irregularly articulated, with indistinct articles (Fig. 2 A–C). Dorsal cirri inserted on cirrophores. Parapodial lobes short, triangular, (Fig. 2 A–C). Ventral cirri digitiform, similar in length or slightly shorter than parapodial lobes (Fig. 2 A–C). Dorsal cirri pseudo-articulated, alternating long cirri, inserted more dorsally (shorter than half of body width) and short cirri, approximately half the length of the long ones, inserted more ventrally; parapodial lobes short, triangular. Compound heterogomph falcigers with subdistal spines, more marked on anterior and dorsal chaetae (Fig. 3A, C); bidentate blades, with short, straight spines on margin, subdistally longer and curved upwards, extending beyond proximal tooth; dorsal and anterior chaetae with both teeth similar, teeth becoming dissimilar progressively along body, more marked on ventral chaetae (Fig. 3A, C); posteriormost ventral compound chaetae with proximal tooth distinctly longer and thicker than distal tooth, with distinctly curved blades and longer subdistal spines. About 14 chaetae anteriorly per parapodium, with elongated blades, progressively reduced to 11 on midbody parapodia (Fig. 3A, C), with dorsoventral gradation in length, changing from anterior (53– 33 μm) (Fig. 3A) to midbody segments (49–42 μm) (Fig. 3C). From midbody backwards, compound chaetae less elongated, with shorter and wider blades, dorso-ventral gradation in length, changing from anterior to posterior, respectively; blades more strongly bidentate, becoming shorter and wider within fascicle ventrally and posteriorly, with proximal tooth becoming larger and more triangular more posterior and ventral (Fig. 3A, C). Dorsal and ventral simple capillary chaetae not seen. Anterior and midbody parapodia with five to six aciculae each, with short, slightly oblique tips (Fig. 3B, D). Pharynx very contracted, about 0.90 mm long, 0.54 mm wide; pharyngeal tooth on anterior margin, surrounded by crown of approximately 10 soft papillae (Fig. 1B). Proventricle, about 2.40 mm long, 1.84 wide, with about 30 muscle cell rows. Reproduction. In members of Megasyllis, sexual reproduction occurs by means of scissiparous schizogamy (San Martín et al. 2014). An incomplete female dicerous stolon was observed attached to the specimen, with approximately 28 segments, yellowish, opaque in alcohol; four orange eyes observed; segments completely filled with yellowish spherical oocytes (Fig. 2C, arrows), about 121 μm in diameter (Fig. 1C), nucleus can be observed (Fig. 1C, arrow). Cirri from stolon thinner and shorter than those of stock. Habitat. Coralline and muddy sand, seagrasses; intertidal to shallow depths (San Martín et al., 2008). Distribution. Originally described from Queensland (Australia) (Hartmann-Schröder, 1991); San Martín et al. (2008) recorded this species also in New South Wales (Australia). First record from the Indian Ocean., Published as part of Rodríguez, Yolanda Lucas, Martín, Guillermo San & Fiege, Dieter, 2019, A new species and nine new records of Syllidae (Annelida) from the Socotra Archipelago (Indian Ocean), pp. 235-258 in Zootaxa 4651 (2) on pages 237-241, DOI: 10.11646/zootaxa.4651.2.2, http://zenodo.org/record/3363175, {"references":["Hartmann-Schroder, G. (1991) Zur Kenntnis des Eulitorals der australischen Kusten unter besonderer Berucksichtigung der Polychaeten und Ostracoden. Teil 16. Die Polychaeten der subtropisch-tropischen bis tropischen Ostkuste Australiens zwischen Maclean (New South Wales) und Gladstone (Queensland) sowie von Heron Island (Groβes Barriere-Riff). Mitteilungen aus dem Hamburgischen Zoologischen Museum und Institut, 88, 17 - 71.","Licher, F. (1999) Revision der Gattung Typosyllis Langerhans, 1879 (Polychaeta: Syllidae). Morphologie, Taxonomie und Phylogenie. Abhandlungen der Senckenbergischen Naturforschenden Gesellschaft, 551, 1 - 336.","San Martin, G., Hutchings, P. & Aguado, M. T. (2008) Syllinae (Polychaeta, Syllidae) from Australia. Part. 2. Genera Inermosyllis, Megasyllis n. gen., Opisthosyllis, and Trypanosyllis. Zootaxa, 1840 (1), 1 - 53. https: // doi. org / 10.11646 / zootaxa. 1840.1.1","San Martin, G., Aguado, M. T. & Alvarez-Campos, P. (2014): Revision of the genus Megasyllis (Annelida, Syllidae) with descriptions of four new species. Journal of the Marine Biological Association of the UK, 94 (2), 331 - 351."]}

Opisthosyllis Langerhans, 1879 Opisthosyllis Langerhans, 1879: 541. Type species: Opisthosyllis brunnea Langerhans, 1879., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2019, A new species and nine new records of Syllidae (Annelida) from the Socotra Archipelago (Indian Ocean), pp. 235-258 in Zootaxa 4651 (2) on page 241, DOI: 10.11646/zootaxa.4651.2.2, http://zenodo.org/record/3363175, {"references":["Langerhans, P. (1879) Die Wurmfauna von Madeira. Zeitschrift fur Wissenschaftliche Zoologie, 33, 513 - 592. https: // doi. org / 10.5962 / bhl. title. 63986"]}

Haplosyllis djiboutiensis Gravier, 1900 Syllis (Haplosyllis) djiboutiensis Gravier 1900: 147���149, pl. 9, fig. 3. Haplosyllis djiboutiensis Lattig & Mart��n 2009: 18, fig. 12.��� Lattig et al. 2010: 10���14, figs. 6, 7.��� Lattig & Martin 2011: figs. 1A���F; 2A, B. Haplosyllis spongicola Imajima 1966 a: 220���221, text-figs. a���h.��� Lee & Rho 1994: 132���134, fig. 1, a���f. Material examined. Socotra, S coast, Steroh, Nogid, 12��19.006N 53��52.845E, 13���15 m, rocky, 14.03.1999, 1 specimen (SMF 24974). Socotra, Qualansiyah Bay, 12��41.026N 53�� 28.309E, 5-6 m, 10.03.1999, 1 specimen (SMF 24975). Socotra, Rhiy di Hamri, 12��40.429N 54��11.731E, 7���9 m, 19.03.1999, 1 specimen, (NHCY 002). Socotra Archipelago, Kal Farun rock outcrop, 12��26.049N 52��08.07E, 9.5���12.5 m, 03.04.2000, 1 specimen (SMF 24977). Habitat. Lattig & Mart��n (2011) recorded high densities of specimens associated with undetermined sponges in Qatar and Abu Dhabi (Persian Gulf). The Socotra Archipelago specimens were found in different types of substrate, including sand, hard substrate, macro algae, turf algae, hard coral, and soft coral. Distribution. Red Sea, Korea, Japan, Australia (Western Australia, South Australia, New South Wales, Northern Territory) (Lattig et al. 2010), Persian Gulf., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2019, A new species and nine new records of Syllidae (Annelida) from the Socotra Archipelago (Indian Ocean), pp. 235-258 in Zootaxa 4651 (2) on page 237, DOI: 10.11646/zootaxa.4651.2.2, http://zenodo.org/record/3363175, {"references":["Gravier, C. (1900) Contribution a l'etude des Annelides Polychetes de la Mer Rouge. Premiere partie. Nouvelles Archives du Museum d'Histoire Naturelle, Paris, 2, 137 - 282.","Lattig, P. & Martin, D. (2009) A Taxonomic Revision of the Genus Haplosyllis Langerhans, 1887 (Polychaeta: Syllidae: Syllinae). Zootaxa, 2220, 1 - 40.","Lattig, P., Martin, D. & San Martin, G. (2010) Syllinae (Syllidae: Polychaeta) from Australia. Part 4. The genus Haplosyllis Langerhans, 1879 (Polychaeta: Syllidae: Syllinae). Zootaxa, 2552, 1 - 36. https: // doi. org / 10.11646 / zootaxa. 2552.1.1","Lattig, P. & Martin, D. (2011) Two new endosymbiotic species of Haplosyllis (Polychaeta: Syllidae) from the Indian Ocean and Red Sea, with new data on H. djiboutiensis from the Persian Gulf. Italian Journal of Zoology, 78, 112 - 23. https: // doi. org / 10.1080 / 11250003.2011.569373","Imajima, M. (1966 a) The Syllidae (Polychaetous Annelids) from Japan (II). Autolytinae. Publications of the Seto Marine Biological Laboratory, 14, 27 - 83. https: // doi. org / 10.5134 / 175422","Lee, J. W. & Rho, B. J. (1994) Systematic studies on Syllidae (Annelida, Polychaeta) from the South Sea and the East Sea in Korea. Korean Journal of Systematic Zoology, 10, 131 - 144."]}

Salvatoria koorineclavata San Mart��n, 2005 Brania clavata Hartmann-Schr��der, 1979: 100, figs. 129���133; 1980: 53; 1990: 53; 1991: 37. Not Clapar��de, 1863. Salvatoria koorineclavata San Mart��n 2005, figs. 11A���G, 12A���E.��� Ding & Westheide 2008:128���131, fig. 3. Material examined. Socotra, N coast, Southeast of Qualansiyah, 12��40.264���N 53��27.204E, from dead coral, 6 m, 08.03.1999, 1 specimen (SMF 24994). Habitat. Common in shallow waters on a variety of substrates to 29 m depth (San Mart��n, 2005). In Socotra in shallow waters among dead corals. Distribution. Australia (all states) (San Mart��n, 2005)., Published as part of Rodr��guez, Yolanda Lucas, Mart��n, Guillermo San & Fiege, Dieter, 2019, A new species and nine new records of Syllidae (Annelida) from the Socotra Archipelago (Indian Ocean), pp. 235-258 in Zootaxa 4651 (2) on page 253, DOI: 10.11646/zootaxa.4651.2.2, http://zenodo.org/record/3363175, {"references":["San Martin, G. (2005) Exogoninae (Polychaeta: Syllidae) from Australia with the description of a new genus and twenty-two new species. Records of the Australian Museum, 57, 39 - 152. https: // doi. org / 10.3853 / j. 0067 - 1975.57.2005.1438","Hartmann-Schroder, G. (1979) Zur Kenntnis des Eulitorals der australischen Kusten unter besonderer Berucksichtigung der Polychaeten und Ostracoden. Teil 2. Die Polychaeten der tropischen Nordwestkuste Australiens (Zwischen Port Samson im Norden und Port Hedland in Suden). Mitteilungen aus dem Hamburgischen Zoologischen Museum und Institut, 76, 75 - 218.","Claparede, E. (1863) Beobachtungen uber Anatomie und Entwicklungsgeschichte wirbelloser Thiere an der Kuste von Nor- mandie angestellt. Wilhelm Engelmann, Leipzig, 120 pp. https: // doi. org / 10.5962 / bhl. title. 10030","Ding, Z. & Westheide, W. (2008) Interstitial Exogoninae from the Chinese coast (Polychaeta, Syllidae). Senckenbergiana biologica, 88, 125 - 159."]}

Trypanosyllis mercedesae n. sp. Figures 4–7 urn:lsid:zoobank.org:act: 99769D77-6407-4F13-84F0-91E4045B875F Material examined. Socotra Archipelago, 12º26.049N 52º08.07E, Kal Farun rock outcrop, 9.5-12.5 m, 03.04.2000. Holotype (including 3 permanent slides with parapodia) (SMF 24983) and one paratype (including 1 permanent slide of a parapodium) (NHCY 005). Diagnosis. Body long, distinctly flattened, with pigmented dorsal cirri, two thin, clearly marked, red-garnet dorsal bands on each anterior segment, up to the proventricular level, relatively short and thick, pigmented dorsal cirri, and almost triangular teeth on the trepan. Description. Holotype longest and complete specimen, 44 mm long, 1.25 mm wide, 281 chaetigers (Fig. 4A); paratype incomplete, without pygidium, 7.8 mm long, 1.28 mm wide, 69 chaetigers. Antennae and tentacular cirri white-yellowish (Fig. 4A, B); dorsal cirri pigmented in garnet or red-wine. Body markedly dorso-ventrally flattened, ribbon-like, and tapered posteriorly. Dorsum of each anterior segment with two transverse red-garnet lines (Fig. 4 A–B,) disappearing progressively some segments after proventricle. Prostomium oval, wider than long, posteriorly bilobed with a conspicuous cleft; two pairs of garnet coloured eyes, in open trapezoidal arrangement; anterior pair larger than posterior one. One pair of palps slightly shorter than prostomium, completely separated, kidney-shaped. Median antenna inserted frontally, near anterior margin of prostomium, with 23–24 articles. Lateral antennae shorter, with 20 articles, emerging slightly behind median antenna. Tentacular segment small, reduced dorsally, with two pairs of tentacular cirri. Dorsal tentacular cirri with 23 articles, ventral ones with 13–15 articles. Dorsal cirri alternating in length; longest cirri slightly longer than body width. First long dorsal cirri about 32–34 articles next ones 27–30 articles; anterior short dorsal cirri about 17–19 articles. Midbody long dorsal cirri with 22–25 articles; midbody short dorsal cirri 11–19. Posterior long dorsal cirri with 23–25 articles; short ones 13–16. Ventral cirri digitiform, shorter than parapodial lobes (Fig. 5 A–C). Anterior parapodia with about 12–13 compound chaetae, with falcigerous blades, bidentate, short spines along margin (Fig. 6A); gradation in length of blades 48 μm long above, 38 μm below. Number and shape of chaetae varying gradually from anterior to posterior parapodia. Midbody parapodia with 6–7 falcigers each, 44 μm above 28 μm below (Fig. 6C), bidentate, proximal tooth small, acute (Fig. 6C), distal tooth larger and also pointed; interspace between distal and proximal tooth wide; proximal part of the blade with small spines on edge; most dorsal ones somewhat elongated and more similar to those of anterior parapodia, with both teeth similar and short spines along edge. Posterior parapodia with similar falcigers as midbody, six per parapodium, 38 μm above (Fig. 6E), 26 μm below. Anterior parapodia with four aciculae each of different sizes, one of them slightly oblique at tip (Fig. 6B); from midbody parapodia, three straight acicula per parapodium, one of them distinctly smaller than other ones (Fig. 6D); posterior aciculae also straight and slightly pointed (Fig. 6F), two per parapodium, one of them smaller. Pharynx brownish, in holotype across approximately 12 segments; proventricle through 16 segments. Pharynx and proventricle of paratype dissected (Fig. 7B); pharynx brownish, through 16 segments, slightly contracted, 1.28 mm long, 0.42 mm surrounded on anterior margin by a crown of 8 finger-shaped papillae (Fig. 7A); trepan with 9–10 brownish triangular teeth (Fig. 7C); proventricle through 13–16 segments (Fig. 7B), 2.1 mm long, 0.57 mm wide, with about 29 muscle cell rows. Pygidium in process of regeneration. Remarks Trypanosyllis mercedesae n. sp. is characterized by having a long body, distinctly flattened, with dorsal cirri pigmented in garnet or red-wine, two slender but clearly marked reddish bands on each anterior segment, up to the proventricular level, relatively short and thick pigmented dorsal cirri, and short almost triangular teeth on trepan. Trypanosyllis richardi is similar and lives in the nearby area of the Red Sea; however, that species has distinctly longer and slender dorsal cirri, which are unpigmented, the two reddish bands on the dorsum of anterior segments are larger, appearing almost as a single, broad band, also present posteriorly to proventricle, and the pharyngeal teeth are longer, not so acute as those of T. mercedesae n. sp. According to WORMS (2019) and Álvarez-Campos et al. (2017, 2018), the genus Trypanosyllis currently consists of about 40 valid species (excluding the species transferred to Trypanedenta Imajima & Hartman, 1964; Trypanoseta Imajima & Hartman, 1964 and Pseudosyllis Grube, 1863). Álvarez-Campos et al. (2017, 2018) revised this genus, and described or re-described numerous species. There are many species of Trypanosyllis with a similar colour pattern, formed by two reddish dorsal bands per segment, at least on anterior segments. Most of the species have both bands slender or one slender and the other larger. Only T. luzonensis (Pillai, 1965), from Philippines, China and Australia, has a similar pattern of pigmentation than T. mercedesae, n. sp., formed by two large bands per segment, appearing to be a single band. However, T. luzonensis has the two bands more marked (sometimes almost fused to each other) and larger than those of T. mercedesae n. sp. and they continue almost to the posterior part of body, while disappearing after the proventricle in T. mercedesae n. sp., the dorsal cirri are long and lacking pigmentation, being much shorter, thicker and pigmented in T. mercedesae n. sp. The compound chaetae in both species are similar, but relatively shorter and less elongated in T. luzonensis. Trypanosyllis krohnii, from W Mediterranean, has a similar colour pattern, but it is proportionally wider, with shorter, unpigmented dorsal cirri, and the compound chaetae are more markedly bidentate (see the re-description in Álvarez-Campos et al. 2017). Habitat. In dead corals at shallow bottoms (9.5 to 12.5 m). Distribution. Only known in Kal Farun rock outcrop, Socotra Archipelago. Etymology. Named after Mª de las Mercedes Rodríguez del Olmo, beloved mother of YLR., Published as part of Rodríguez, Yolanda Lucas, Martín, Guillermo San & Fiege, Dieter, 2019, A new species and nine new records of Syllidae (Annelida) from the Socotra Archipelago (Indian Ocean), pp. 235-258 in Zootaxa 4651 (2) on pages 242-247, DOI: 10.11646/zootaxa.4651.2.2, http://zenodo.org/record/3363175, {"references":["Alvarez-Campos, P., Giribet, G., San Martin, G., Rouse, G. W. & Riesgo, A. (2017) Straightening the striped chaos: systematics and evolution of Trypanosyllis and the case of its pseudo-cryptic type species Trypanosyllis krohnii (Annelida, Syllidae). Zoological Journal of the Linnean Society, 179, 492 - 540. https: // doi. org / 10.1111 / zoj. 12443","Imajima, M. & Hartman, O. (1964) The polychaetous annelids of Japan. Allan Hancock Foundation Occasional Papers, 26, 1 - 452.","Pillai, T. G. (1965) Annelida Polychaeta from the Philippines and Indonesia. Ceylon Journal of Science, 5 (2), 109 - 177."]}

Myrianida pachycera (Augener, 1913) Autolytus pachycerus Augener, 1913: 257–260, pl. 2, fig. 11, 12, text-fig. 40A–C; 1927: 157–158.— Nygren & Sundberg 2003: GenBank sequences, 16S rDNA partial sequence AF474258, and 18S rDNA partial sequence AF474304. Myrianida pachycera Imajima 1966b: 79–82, fig. 26A–L.— Imajima 1967: 417. Myrianida pachycerus Hartman 1966: 362–363, fig. 1A–B. Autolytus purpureimaculata Okada 1933: 332–338, figs. 6–11; 1937.— Imajima & Hartman 1964: 100. Myrianida crassicirrata Hartmann-Schröder, 1965: 119–121, figs. 47–49. Material examined. Socotra, Samhah Island, intertidal, amongst algae, 12º10’99N / 53º04’23E, algae, 07.04.2000, 1 specimen (SMF 24995). Remarks. One female specimen with 28 segments up to beginning of the stolons, 3.8 mm long, 0.64 mm wide, yellowish coloration, cirri with same length along the body up to formation of stolon. A line of five stolons attached in different stages of maturation. Specimen very fragile. Four red eyes arranged in open trapezoidal arrangement. Nuchal epaulettes not visible. Palps fused along all their length. No ciliation observed in dorsal view. Median antenna thick, flat reaching almost chaetiger 10. Lateral antennae and ventral tentacular cirri 1/2 length of median antenna. Lateral antennae and tentacular cirri cylindrical, annulated. Almost all cirri lost on left side. First dorsal cirri similar in length to lateral antennae. Second dorsal cirri ¾ length of median antenna, thick and flat. Cirri 3 to 8 alternate in length short/long and in thick/flat shape. Schizogamous reproduction by gemmiparity, behind either chaetiger 31 or 34 (Nygren, 2004). Habitat. Intertidal, shallow depths, together with rich epifauna (Nygren, 2004); in Socotra also amongst algae. Distribution. East Indian Ocean, Pacific, West Atlantic. Australia, Japan, Hawaii, California, Florida (Nygren, 2004)., Published as part of Rodríguez, Yolanda Lucas, Martín, Guillermo San & Fiege, Dieter, 2019, A new species and nine new records of Syllidae (Annelida) from the Socotra Archipelago (Indian Ocean), pp. 235-258 in Zootaxa 4651 (2) on pages 253-254, DOI: 10.11646/zootaxa.4651.2.2, http://zenodo.org/record/3363175, {"references":["Augener, H. (1913) Polychaeta I, Errantia. Die Fauna Sudwest-Australiens. Ergebnisse der Hamburger sudwest-australischen Forschungreise, 4 (5), 65 - 304. [1905]","Nygren, A. & Sundberg, P. (2003) Phylogeny and evolution of reproductive modes in Autolytinae (Syllidae, Annelida). MolecularPhylogeny and Evolution, 29, 235 - 249. https: // doi. org / 10.1016 / S 1055 - 7903 (03) 00095 - 2","Imajima, M. (1966 b) The Syllidae (Polychaetous Annelids) from Japan (IV). Syllinae (1). Publications of the Seto Marine Biological Laboratory, 14, 219 - 252. https: // doi. org / 10.5134 / 175436","Imajima, M. (1967) Errant polychaetous annelids from Tsukumo Bay and vicinity of Noto Peninsula, Japan. Bulletin of the National Science Museum Tokyo, 10, 403 - 441.","Hartman, O. (1966) Polychaetous annelids of the Hawaiian Islands. Occasional Papers of the Bernice P. Bishop Museum, 23, 163 - 252.","Okada, Y. K. (1933) Two interesting syllids, with remarks on their asexual reproduction. Memoires of the College of Science, Kyoto Imperial University, Series B, 8, 325 - 339.","Imajima, M. & Hartman, O. (1964) The polychaetous annelids of Japan. Allan Hancock Foundation Occasional Papers, 26, 1 - 452.","Hartmann-Schroder, G. (1965) Zur Kenntnis der eulitoralen Polychaetenfauna von Hawaii, Palmyra und Samoa. Abhandlungen und Verhandlungen des Naturwissensschaftlichen Vereins in Hamburg, Supplement 9, 81 - 161.","Nygren, A. (2004) Revision of Autolytinae (Syllidae: Polychaeta). Zootaxa, 680 (1), 1 - 314. https: // doi. org / 10.11646 / zootaxa. 680.1.1"]}

Reuscher, Michael G., Fiege, Dieter (2016): Ampharetidae (Annelida: Polychaeta) from cold seeps off Pakistan and hydrothermal vents off Taiwan, with the description of three new species. Zootaxa 4139 (2): 197-208, DOI: http://doi.org/10.11646/zootaxa.4139.2.4

Glyphanostomum bilabiatum sp. nov. (Figs 4 A���F; 7B) Specimens examined. Holotype: SMF 24137, Yonaguni Knoll IV Hydrothermal Vent Field, high CO2 seepage site, Okinawa Trough, 24��50.777���N 122��42.039���E, 1365 m, SO 196, Station 49, TV-MUC, 17 March 2008 (cs). Paratype: SMF 24138, Yonaguni Knoll IV Hydrothermal Vent Field, low CO2 seepage site, Okinawa Trough, 24��50.775���N 122��42.049���E, 1385 m, SO 196, Station 39, TV-MUC, 14 March 2008 (1 cs). Description. Length 1.8 mm, width 0.38 mm. Prostomium with middle lobe delimited by incision from surrounding lobe, without glandular ridges or eyes. Only tips of buccal tentacles visible. Segment II forming one continuous prominent ventral and ventrolateral lappet (Fig. 4 A). Three pairs of slender, cirriform branchiae, arranged in one transverse row in segment III, not separated by median gap; innermost branchia of right group missing; second outermost branchiae of transverse row originating from segment II, outermost branchiae of transverse row originating from segment III, innermost branchiae of transverse row originating from segment IV (Fig. 7 B). Segment II without chaetae. Notopodia with capillary chaetae from segment III, present in 14 chaetigers; first pair of notopodia much smaller than in following chaetigers; notopodia of thoracic unciniger 8 slightly elevated and connected by prominent dorsal glandular ridge (Fig. 4 B); ventral papilla in notopodia of thoracic unciniger 8, absent in other notopodia; capillary chaetae of elevated notopodia broken and indeterminable. Neuropodial tori with uncini from segment VI, present in 11 thoracic uncinigers; tori without cirri. Continuous ventral shields conspicuous to thoracic unciniger 9. Two intermediate uncinigers (Fig. 4 C). Nine abdominal uncinigers without rudimentary notopodia. Pinnules without dorsal cirrus. Each pair of pinnules connected by dorsal glandular stripe (Fig. 4 C, D). Pygidium with terminal anus and one pair of short, stout, ventrolateral anal cirri (Fig. 4 D). Uncini in thoracic and intermediate uncinigers with 7���8 teeth in 2 vertical rows over rostral tooth and basal prow (Fig. 4 E). Uncini in abdominal uncinigers with 10 teeth in 3 vertical rows over rostral tooth and basal prow (Fig. 4 F). Remarks. In the paratype specimen the two branchial groups are separated by a small median gap of about half the branchial width and the capillary chaetae of the elevated notopodia are not modified. The paratype specimen is 5.5 mm long and 0.6 mm wide. Glyphanostomum bilabiatum sp. nov. is unique within the genus because of the modified and elevated notopodia, connected by a dorsal ridge in thoracic unciniger 8. Lateral lappets in segment II have also been described in the congeneric species G. moreirai Aguirrezabalaga & Parapar, 2014 and G. hesslei Reuscher, Fiege & Imajima, 2015. However, in these species the lappets were relatively small and restricted to the sides of segment II. In the new species there is one continuous lappet that stretches from side to side, across the ventrum of segment II, reminiscent of lateral lappets in anterior segments of some terebellid genera. Ventrally the lappet looks like a second lower lip. The modified thoracic unciniger 8 is remarkably similar to the typical modification in the genera Anobothrus and Zatsepinia. The holotype was collected in the northern area of the Abyss vent. The area was characterized by high CO2 seepage. The sediment had a distinct H2S smell. At the collection site of the paratype gas bubbles were observed, even though it had a lower CO2 seepage rate (Rehder et al. 2008). Etymology. The species name refers to the ventral lappet in segment II, which looks like a second lower lip. Distribution. Exclusively known from the Yonaguni Knoll IV Hydrothermal Field in the Okinawa Trough off the northeastern coast of Taiwan., Published as part of Reuscher, Michael G. & Fiege, Dieter, 2016, Ampharetidae (Annelida: Polychaeta) from cold seeps off Pakistan and hydrothermal vents off Taiwan, with the description of three new species, pp. 197-208 in Zootaxa 4139 (2) on pages 202-204, DOI: 10.11646/zootaxa.4139.2.4, http://zenodo.org/record/262112, {"references":["Aguirrezabalaga, F. & Parapar, J. (2014) Deep-sea Ampharetidae (Polychaeta) from Capbreton Canyon (north-east Atlantic) with the description of a new species. Journal of the Marine Biological Association of the United Kingdom, 94, 947 - 967. http: // dx. doi. org / 10.1017 / S 0025315413001422","Reuscher, M., Fiege, D. & Imajima, M. (2015) Ampharetidae (Annelida: Polychaeta) from Japan. Part IV. Miscellaneous genera. Journal of the Marine Biological Association of the United Kingdom, 95 (6), 1105 - 1125. http: // dx. doi. org / 10.1017 / S 0025315415000545","Rehder, G., Schneider von Deimling, J. & cruise participants (2008) RV Sonne Cruise Report SO 196, SUMSUN 2008, Suva - Guam - Okinawa Trough - Manila, February 19 - March 26, 2008. Leibniz Institut fur Ostseeforschung, Sektion Meereschemie, Warnemunde, 69 pp."]}

Anobothrus dayi Imajima, Reuscher & Fiege, 2013 (Fig 2 A, B) Specimens examined. SMF 24135, Yonaguni Knoll IV Hydrothermal Field, sampling site not affected by CO2 seepage, Okinawa Trough, 24��50.355���N 122��41.736���E, 1324 m, SO 196, Station 65, TV-MUC, 18 March 2008 (1 af). Description. Anterior fragment including ten thoracic uncinigers. Length 1.2 mm, width 0.35 mm. Prostomium with middle lobe delimited by incision from surrounding lobe, without glandular ridges or eyes. Buccal tentacles with ventral groove, smooth. Three pairs of cirriform branchiae in fused segments II + III, arranged in transverse row; groups of branchiae separated by wide median gap (Fig. 2 A); segmental origin of outermost and second outermost branchiae not determinable; branchiae of segment IV inserted in innermost position of transverse row. Chaetae in fused segments II + III longer and slightly thicker than following capillaries, pointing forwards. Notopodia with limbate capillary notochaetae from segment IV, present to end of fragment. Notopodia in thoracic unciniger 8 slightly elevated, connected by dorsal ridge (Fig. 2 A); notochaetae of thoracic unciniger 8 broken, shape indeterminable. Neuropodial tori with uncini from segment VI, present to end of fragment. Cirri and papillae in thoracic parapodia absent. Circular glandular band absent. Continuous ventral shields present to thoracic unciniger 9. Intermediate and abdominal uncinigers missing. Nephridial papillae absent. Thoracic uncini with 9 teeth in 2 alternating rows above rostral tooth and basal prow (Fig. 2 B). Distribution. Anobothrus dayi has been found along the coast of Japan, in depths of 30���125 m (Imajima et al. 2013). The finding at the Yonaguni Knoll Hydrothermal Field is the species��� second record. It was found in an area that is not directly affected by the hydrothermal vent���s CO2 seepage. It is the deepest and southernmost record of the species., Published as part of Reuscher, Michael G. & Fiege, Dieter, 2016, Ampharetidae (Annelida: Polychaeta) from cold seeps off Pakistan and hydrothermal vents off Taiwan, with the description of three new species, pp. 197-208 in Zootaxa 4139 (2) on page 200, DOI: 10.11646/zootaxa.4139.2.4, http://zenodo.org/record/262112, {"references":["Imajima, M., Reuscher, M. G. & Fiege, D. (2013) Ampharetidae (Annelida: Polychaeta) from Japan. Part II: Genera with elevated and modified notopodia. Zootaxa, 3647 (1), 137 - 166. http: // dx. doi. org / 10.11646 / zootaxa. 3647.1.7"]}

Eclysippe yonaguniensis sp. nov. (Figs 3 A���C; 7A) Specimens examined. Holotype: SMF 24136, Yonaguni Knoll IV Hydrothermal Field, low CO2 seepage site, Okinawa Trough, 24��50.355���N 122��41.736���E, 1324 m, SO 196, Station 65, TV-MUC, 18 March 2008 (cs, broken into 3 pieces during examination). Description. Length 1.9 mm, width 0.16 mm. Prostomium triangular with conical front, without lobes, incisions, glandular ridges or eyes (Fig. 3 A). Buccal tentacles smooth, with ventral groove (Fig. 3 B). Three pairs of smooth cirriform branchiae arranged in one transverse row in segment III, separated by median gap of about twice the branchial width; outermost and second outermost branchiae of right group missing; innermost branchiae short and digitiform, less than half as long as remaining branchiae (Fig. 3 A); second outermost branchiae of transverse row originating from segment II, outermost branchiae of transverse row originating from segment III, median branchiae originating from segment IV (Fig. 7 A). Segment II with enlarged chaetae, formed as paleae; three paleae in left group, four in right group (Fig. 3 B). Notopodia with capillary chaetae from segment III, present in 15 chaetigers; first two pairs of notopodia very small, gradually increasing in size to fourth pair, decreasing again from twelfth pair; notopodia without cirri (Fig. 3 A). Notochaetae of first two and last four thoracic uncinigers fewer in number, thinner and shorter than those in median thoracic notopodia. Neuropodial tori with uncini from segment VI, present in 12 thoracic uncinigers; tori without cirri. Continuous ventral shields present to thoracic unciniger 8. Segment length gradually increasing between thoracic unciniger 7 and 9; each of thoracic uncinigers 9���12 about as long as first six thoracic uncinigers combined (Fig. 3 A). Two intermediate uncinigers (Fig. 3 C). Eight abdominal uncinigers without rudimentary notopodia. Pinnules without dorsal cirrus. Pygidium with terminal anus and two short stout ventrolateral anal cirri. Uncini in thoracic, intermediate and abdominal uncinigers with numerous teeth in two alternating rows over rostral tooth and basal prow. Remarks. Eclysippe yonaguniensis sp. nov. differs from E. trilobata by the possession of very short branchiae in the innermost position of the transverse row. In E. vanelli the innermost branchiae are unknown because they were missing in Fauvel���s (1936) and Eliason���s (1955) specimens. Eclysippe vanelli and E. trilobata were both described with modified notopodia in the last five thoracic uncinigers. In the new species the last five notopodia are slightly reduced in size, but their shape is not different. Furthermore, both E. trilobata and E. vanelli have much smaller gaps between branchial groups and a higher count of paleae (around 10). Eclysippe vanelli was described with 12 (Eliason 1955), E. trilobata with 12���14 (Hilbig 2000) abdominal uncinigers. Because the number of intermediate uncinigers (sensu Imajima et al. 2012), i.e., segments that have neuropodia of the thoracic type but lack notopodia, is constant within a genus, we assume that the first two uncinigers that were included in the counts of abdominal uncinigers of these species are actually intermediate uncinigers. Therefore, the adjusted counts of abdominal uncinigers in E. vanelli, E. trilobata, are assumed to be 10 and 10���12, respectively, whereas Eclysippe yonaguniensis sp. nov. has only 8 abdominal uncinigers. Distribution. Exclusively known from the Yonaguni Knoll IV Hydrothermal Field in the Okinawa Trough off the northeastern coast of Taiwan., Published as part of Reuscher, Michael G. & Fiege, Dieter, 2016, Ampharetidae (Annelida: Polychaeta) from cold seeps off Pakistan and hydrothermal vents off Taiwan, with the description of three new species, pp. 197-208 in Zootaxa 4139 (2) on page 201, DOI: 10.11646/zootaxa.4139.2.4, http://zenodo.org/record/262112, {"references":["Eliason, A. (1955) Neue oder wenig bekannte schwedische Ampharetiden (Polychaeta). GOteborgs Kungliga Vetenskaps- och Vitterhets-Samhalles Handlingar, 6 (16), 1 - 17.","Hilbig, B. (2000) Family Ampharetidae Malmgren, 1866. In: Blake, J. A., Hilbig, B. & Scott, P. V. (Eds.), Taxonomic atlas of the benthic fauna of the Santa Maria Basin and Western Santa Barbara Channel. The Annelida Part 4. Polychaeta: Flabelligeridae to Sternaspidae. Santa Barbara Museum of Natural History, Santa Barbara, pp. 169 - 230.","Imajima, M., Reuscher, M. G. & Fiege, D. (2012) Ampharetidae (Annelida: Polychaeta) from Japan. Part I: The genus Ampharete Malmgren, 1866, along with a discussion of several taxonomic characters of the family and the introduction of a new identification tool. Zootaxa, 3490, 75 - 88."]}

Glyphanostomum Levinsen, 1884 Type species: Samytha pallescens Th��el, 1879 Generic diagnosis (emended). Prostomium without glandular ridges. Buccal tentacles smooth. Three pairs of cirriform branchiae. Segment II without chaetae. Thorax with 14 chaetigers and 11 uncinigers. Modified thoracic unciniger 8 with elevated notopodia and dorsal glandular ridge absent or present. Two intermediate uncinigers. Abdominal rudimentary notopodia absent. Remarks. The generic diagnosis had to be emended to accommodate the newly described species, which has a modified segment in the posterior thorax, reminiscent of the modification in the genera Anobothrus and Zatsepinia Jirkov, 1986. We decided against the erection of a new genus because all morphological characters, with the exception of the modified segment, agree with the generic diagnosis of Glyphanostomum. In contrast, Anobothrus, which is distinguished by a similar modification from Ampharete has additional morphological differences, most notably smooth, rather than pinnate, buccal tentacles., Published as part of Reuscher, Michael G. & Fiege, Dieter, 2016, Ampharetidae (Annelida: Polychaeta) from cold seeps off Pakistan and hydrothermal vents off Taiwan, with the description of three new species, pp. 197-208 in Zootaxa 4139 (2) on page 202, DOI: 10.11646/zootaxa.4139.2.4, http://zenodo.org/record/262112, {"references":["Levinsen, G. M. R. (1884) Systematisk-geografisk Oversigt over de nordiske Annulata, Gephyrea, Chaetognathi og Balanoglossi. Videnskabelige Meddelelser fra den naturhistoriske Forening i KjObenhavn, 1883, 92 - 350.","Theel, H. J. (1879) Les Annelides Polychetes des mers de la Nouvelle-Zemble. Kungliga Svenska Vetenskaps-Akademiens Handlingar, 16 (3), 1 - 75.","Jirkov, I. A. (1986) [Zatsepinia rittichae gen. et sp. n. (Polychaeta, Ampharetidae) from the Norwegian and Barents Seas]. Zoologicheskii Zhurnal, 65 (2), 289 - 290. [in Russian]"]}

Amage Malmgren, 1866 Type species: Amage auricula Malmgren, 1866 Paramage Caullery, 1944 Egamella Fauchald, 1972 Mexamage Fauchald, 1972 Generic diagnosis. Prostomium with middle lobe surrounded by inflated lobe, lacking glandular ridges. Buccal tentacles smooth. Two to four pairs of cirriform branchiae. Segment II usually without chaetae, or exceptionally with minute chaetae. Thorax with 11���14 uncinigers. Modified or intermediate segments absent. Abdomen with rudimentary notopodia. Remarks. With the description of new Amage species with unusual features (Sch��ller & Jirkov 2013; Reuscher et al. 2015) and the proposed synonymy of Amage with other genera (Jirkov 2011), the generic diagnosis has become quite inclusive. A revision of Amage is urgently needed to determine if this is justified, or if the genus needs to be split., Published as part of Reuscher, Michael G. & Fiege, Dieter, 2016, Ampharetidae (Annelida: Polychaeta) from cold seeps off Pakistan and hydrothermal vents off Taiwan, with the description of three new species, pp. 197-208 in Zootaxa 4139 (2) on page 198, DOI: 10.11646/zootaxa.4139.2.4, http://zenodo.org/record/262112, {"references":["Malmgren, A. J. (1866) Nordiska Hafs-Annulater. Ofversigt af Kongliga Vetenskaps-Akademiens FOrhandlingar, 5, 355 - 410.","Caullery, M. (1944) Polychetes sedentaires de l'expedition du Siboga. Ariciidae, Spionidae, Chaetopteridae, Chlorhaemidae, Opheliidae, Oweniidae, Sabellariidae, Sternaspidae, Amphictenidae, Ampharetidae, Terebellidae. Siboga-Expeditie. Utkomsten op zoologisch, botanisch, oceanographisch en geologisch Gebied verzameld in Nederlandsch Oost-Indie 1899 - 1900 aan Boord H. M. Siboga onder Commando van Luitenant ter zee 1. kl. G. F. Tydeman, 24 (2), 1 - 204.","Fauchald, K. (1972) Benthic polychaetous annelids from deep water off western Mexico and adjacent areas in the Eastern Pacific Ocean. Allan Hancock Monographs in Marine Biology, 7, 1 - 575.","Schuller, M. & Jirkov, I. A. (2013) New Ampharetidae (Polychaeta) from the deep Southern Ocean and shallow Patagonian waters. Zootaxa, 3692 (1), 204 - 237. http: // dx. doi. org / 10.11646 / zootaxa. 3692.1.11","Reuscher, M., Fiege, D. & Imajima, M. (2015) Ampharetidae (Annelida: Polychaeta) from Japan. Part IV. Miscellaneous genera. Journal of the Marine Biological Association of the United Kingdom, 95 (6), 1105 - 1125. http: // dx. doi. org / 10.1017 / S 0025315415000545","Jirkov, I. A. (2011) Discussion of taxonomic characters and classification of Ampharetidae (Polychaeta). Italian Journal of Zoology, 78, 78 - 94. http: // dx. doi. org / 10.1080 / 11250003.2011.617216"]}

Pavelius makranensis sp. nov. (Figs 5 A���D; 6A���E; 7C) Specimens examined. Holotype: SMF 24139, Flare 2 cold seep, Makran accretionary prism, continental margin of Pakistan, 24��50.753���N 63��01.439���E, 1025 m, M 74/3, ROV Dive 181, push core, 6 November 2007 (cs, male). Paratype: SMF 24140, same station data as holotype (1 cs, female). Paratype: SMF 24141, same station data as holotype (1 cs, female). Paratypes: SMF 24142, Flare 2 cold seep, Makran accretionary prism, continental margin of Pakistan, 24��50.829���N 63��01.419���E, 1038 m, M 74/3, ROV Dive 180, sampling net, 5 November 2007 (1 cs, male). Paratypes: SMF 24143, Flare 2 cold seep, Makran accretionary prism, continental margin of Pakistan, 24��50.829���N 63��01.419���E, 1038 m, M 74/3, ROV Dive 180, sampling net, 5 November 2007 (4 cs, 3 af, 4 females, 3 males, plus 3cs used for SEM, stub-nos. 1199���1201). Additional material examined. SMF 24144, Flare 2 cold seep, Makran accretionary prism, continental margin of Pakistan, 24��50.829���N 63��01.419���E, 1038 m, M 74/3, ROV Dive 180, sampling net, 5 November 2007 (2af, 1 female, 1 male). Another specimen from the same station was used for DNA analysis. Description. Length 11.7 mm, width 1.6 mm. Prostomium with lateral incisions delimiting middle section, not reaching anterior end; prostomial glandular ridges absent; paired lateral dark pigment stripes in prostomium (Fig. 5 A). Buccal tentacles smooth. Four pairs of smooth cirriform branchiae arranged in one transverse row in segment III, not separated by median gap; branchiae with very densely arranged thick branchiophores, tapering distally; second outermost branchiae of transverse row originating from segment II, outermost branchiae of transverse row originating from segment III, innermost branchiae of transverse row originating from segment IV, second innermost branchiae of transverse row originating from segment V (Fig. 7 C). Segment II with small chaetae, resembling capillary notochaetae of following segments; chaetae of segment II emerging from notopodia like humps, located more ventrally than notopodia (Fig. 5 A). Notopodia with capillary chaetae (Fig. 6 A) from segment III, present in 15 chaetigers; first pair of notopodia smaller than following ones; first three pairs of notopodia slightly elevated dorsally above following notopodia; notopodia without cirri. Large nephridial papillae above notopodia of first unciniger (Figs. 5 A, 6B). Neuropodial tori with uncini from segment VI, present in 12 thoracic uncinigers; tori without cirri. Continuous ventral shields conspicuous to thoracic unciniger 10, faint in thoracic unciniger 11. Two intermediate uncinigers (Fig. 5 B). Sixteen abdominal uncinigers. Rudimentary notopodia present as small papillae in intermediate uncinigers and first abdominal unciniger (Fig. 5 B), absent in remaining abdominal uncinigers. Pinnules without dorsal cirrus (Fig. 5 C). Pygidium with terminal anus but without anal cirri. Thoracic uncini with unpaired tooth on top and paired median teeth over rostral tooth and basal prow, framed by small lateral teeth (Fig. 6 C, D). Abdominal uncini with about seven teeth over rostral tooth and basal prow (Fig. 6 E). Tube made of dark grey clay. Remarks. The large nephridial papillae are presumably only present in male specimens. They were lacking in every specimen that contained eggs and vice versa. The prostomial dark pigment stripes in the holotype and several paratype specimens probably belong to nuchal organs. In some paratype specimens the area behind the lateral incisions of the prostomium lacked the dark pigment. Instead, they appeared to be brightly colored nuchal organs (Fig. 5 D). About half of the complete paratype specimens had ventrolateral papillae in their pygidia, while the other half and the holotype did not. It seems that Pavelius makranensis sp. nov. can contract the pygidium and withdraw the anal papillae. The only congener Pavelius uschakovi Kuznetsov & Levenstein, 1988 has 21 abdominal uncinigers (assuming that the first two of the 23 abdominal segments mentioned in the original description are actually intermediate uncinigers), five more than in the new species. P. makranensis sp. nov. has notopodial rudiments in the intermediate uncinigers and the first abdominal unciniger, whereas they are lacking in P. uschakovi. Finally, the abdominal uncini of P. uschakovi were described with five teeth. The new species has abdominal uncini with seven teeth. The type specimen of P. uschakovi was not available for examination because it is lost (Budaeva, pers. comm.). The new species had been tentatively identified as Pavelius uschakovi in an ecological study of the Makran accretionary prism (Fischer et al. 2011). They noted that the species dominated a transitional area between a central microbial mat and a peripheral vesicomyid clam bed. The only other described congener P. uschakovi has been recorded from the Paramushir gas hydrate seep in the Sea of Okhotsk and from gas hydrates on the Cascadia margin (Sahling et al. 2002). A presumably undescribed species was recorded from the coast off Natuna Island in the China Sea (Al-Hakim & Glasby 2004). No mention of gas hydrate seeps was made in the latter case. Unfortunately, DNA sequencing for three genes, i.e. COI, 16S rDNA and 18s rDNA, did not yield contiguous sequences. Possible explanations might be insufficient fixation or subsequent storage of samples under ambient conditions. Etymology. The new species is named after its sampling location, the Makran accretionary prism. Distribution. Exclusively known from cold seeps of the Makran accretionary prism off the coast of Pakistan., Published as part of Reuscher, Michael G. & Fiege, Dieter, 2016, Ampharetidae (Annelida: Polychaeta) from cold seeps off Pakistan and hydrothermal vents off Taiwan, with the description of three new species, pp. 197-208 in Zootaxa 4139 (2) on pages 204-206, DOI: 10.11646/zootaxa.4139.2.4, http://zenodo.org/record/262112, {"references":["Kuznetsov, A. P. & Levenstein, R. Y. (1988) [Pavelius uschakovi gen. et sp. n. (Polychaeta, Ampharetidae) from Paramushir Gas Hydrate Spring in the Okhotsk Sea]. Zoologicheskii Zhurnal, 67 (6), 819 - 825. [in Russian]","Fischer, D., Sahling, H., Nothen, K., Bohrmann, G., Zabel, M. & Kasten, S. (2011) Interaction between hydrocarbon seepage, chemosynthetic communities and bottom water redox at cold seeps of the Makran accretionary prism: insights from habitatspecific pore water sampling and modeling. Biogeosciences Discussions, 8, 9763 - 9811. http: // dx. doi. org / 10.5194 / bgd- 8 - 9763 - 2011","Sahling, H., Rickert, D., Lee, R. W., Linke, P. & Suess, E. (2002) Macrofaunal community structure and sulfide flux at gas hydrate deposits from the Cascadia convergent margin, NE Pacific. Marine Ecology Progress Series, 231, 121 - 138. http: // dx. doi. org / 10.3354 / meps 231121","Al-Hakim, I. & Glasby, C. J. (2004) Polychaeta (Annelida) of the Natuna Islands, South China Sea. Raffles Bulletin of Zoology Supplement, 11, 25 - 45."]}

Anobothrus Levinsen, 1884 Type species: Ampharete gracilis Malmgren, 1866 Sosanides Hartmann-Schr��der, 1965 Anobothrella Hartman, 1967 Melythasides Desbruy��res, 1978 Generic diagnosis. Prostomium with middle lobe delimited by incision from surrounding lobe, without glandular ridges. Buccal tentacles smooth or papillose. Three to four pairs of cirriform branchiae, all arising from fused segments II+III. Notochaetae originating from segment II, if present, varying in size from regular notochaetae size to strongly enlarged. Eleven or twelve thoracic uncinigers. One anterior unciniger may have a circular glandular band. Fourth-, fifth-, or sixth-to-last thoracic unciniger with one or more modifications: elevated notopodia, glandular ridge between notopodia, modified notochaetae. Two intermediate segments. Abdominal rudimentary notopodia absent., Published as part of Reuscher, Michael G. & Fiege, Dieter, 2016, Ampharetidae (Annelida: Polychaeta) from cold seeps off Pakistan and hydrothermal vents off Taiwan, with the description of three new species, pp. 197-208 in Zootaxa 4139 (2) on page 199, DOI: 10.11646/zootaxa.4139.2.4, http://zenodo.org/record/262112, {"references":["Levinsen, G. M. R. (1884) Systematisk-geografisk Oversigt over de nordiske Annulata, Gephyrea, Chaetognathi og Balanoglossi. Videnskabelige Meddelelser fra den naturhistoriske Forening i KjObenhavn, 1883, 92 - 350.","Malmgren, A. J. (1866) Nordiska Hafs-Annulater. Ofversigt af Kongliga Vetenskaps-Akademiens FOrhandlingar, 5, 355 - 410.","Hartmann-Schroder, G. (1965) Die Polychaeten des Sublitorals. In: Hartmann-Schroder, G. & Hartmann, G. (Eds.), Zur Kenntnis des Sublitorals der chilenischen Kuste unter besonderer Berucksichtigung der Polychaeten und Ostracoden. (Mit Bemerkungen uber den Einfluss sauerstoffarmer StrOmungen auf die Besiedlung von marinen Sedimenten). Mitteilungen aus dem Hamburgischen zoologischen Museum und Institut 62 (Erganzungsband), Hamburg, pp. 59 - 305.","Hartman, O. (1967) Polychaetous annelids collected by the USNS Eltanin and Staten Island cruises, chiefly from Antarctic Seas. Allan Hancock Monographs in Marine Biology, 2, 1 - 387.","Desbruyeres, D. (1978) Melythasides laubieri gen. sp. nov. Ampharetidae (Annelides Polychetes sedentaires) abyssal de la mer de Norvege. Bulletin du Museum d'Histoire Naturelle, Paris, 353 (514), 231 - 238."]}

Pavelius Kuznetsov & Levenstein, 1988 Type species: Pavelius uschakovi Kuznetsov & Levenstein, 1988 Generic diagnosis (emended). Prostomium without lobes or glandular ridges. Buccal tentacles smooth. Four pairs of branchiae. Notochaetae in segment II present, followed by fifteen thoracic chaetigers. Twelve thoracic uncinigers. Two intermediate uncinigers. Males with one pair of nephridial papillae above notopodia of first thoracic unciniger. Remarks. The generic diagnosis was emended to accommodate our findings in the newly described species. The genus was described lacking notopodial rudiments, which we found in the intermediate uncinigers and first abdominal unciniger. The large nephridial papillae above the notopodia of the first thoracic unciniger only seem to occur in male specimens. We do not follow Jirkov (2001, 2011), who suggested to synonymize Pavelius with Phyllocomus Grube, 1878. Phyllocomus is characterized by strongly modified branchiae and a very large number of abdominal uncinigers.

Eclysippe Eliason, 1955 Type species: Lysippe vanelli Fauvel, 1936 Generic diagnosis. Prostomium without glandular ridges. Buccal tentacles smooth. Three pairs of cirriform branchiae. Notochaetae of segment II enlarged as paleae. Twelve thoracic uncinigers. Posterior thoracic uncinigers strongly elongated. Two intermediate uncinigers. Abdominal rudimentary notopodia absent. Remarks. Curiously, both valid species of the genus, Eclysippe vanelli (Fauvel, 1936) and E. trilobata (Hartman, 1969) were originally described with four pairs of branchiae. Eliason (1955) accredited Fauvel���s diagnosis to a misinterpretation of notopodia as bases of the fourth pair of broken branchiae and redescribed the species Lysippe vanelli in the new genus Eclysippe Eliason, 1955. This new diagnosis of E. vanelli has been widely accepted (e.g. Holthe 1986; Hilbig 2000). E. trilobata, described as Anobothrus by Hartman (1969), was redescribed with three pairs of branchiae by Williams (1987) upon examination of the type specimens and assigned to Eclysippe. Day (1973) argued that specimens of E. vanelli described by Eliason (1955) were different from specimens reported by Fauvel (1936) and subsequently described a new species, Samythella eliasoni Day, 1973 from North Carolina, which, according to Day, was identical to the Swedish E. vanelli specimens described by Eliason (1955). However, he assigned the species to Samythella because of the uncertainty in the number of branchiae in Eclysippe (see discussion above) and because it fit into the generic diagnosis of Samythella according to his opinion. We do not follow Day���s opinion because the latter genus lacks the elongation of posterior thoracic uncinigers that is characteristic for Eclysippe. Furthermore, Samythella has broad, foliaceus branchiae, whereas Eclysippe has thin cylindrical branchiae. In his description of S. eliasoni Day did not mention the elongation of posterior thoracic uncinigers, which is the most conspicuous character of Eclysippe. Therefore, the generic affiliation of S. eliasoni is uncertain. Day (1963) described another species, Samythella affinis Day, 1963 that bears some resemblance to Eclysippe, even though Day did not mention the elongated posterior thoracic uncinigers and acknowledged that the generic affiliation of this species was uncertain., Published as part of Reuscher, Michael G. & Fiege, Dieter, 2016, Ampharetidae (Annelida: Polychaeta) from cold seeps off Pakistan and hydrothermal vents off Taiwan, with the description of three new species, pp. 197-208 in Zootaxa 4139 (2) on pages 200-201, DOI: 10.11646/zootaxa.4139.2.4, http://zenodo.org/record/262112, {"references":["Eliason, A. (1955) Neue oder wenig bekannte schwedische Ampharetiden (Polychaeta). GOteborgs Kungliga Vetenskaps- och Vitterhets-Samhalles Handlingar, 6 (16), 1 - 17.","Fauvel, P. (1936) Contribution a la faune des annelides polychetes du Maroc. Memoires de la Societe des Sciences Naturelles du Maroc, 43, 1 - 143.","Hartman, O. (1969) Atlas of the sedentariate polychaetous annelids from California. Allan Hancock Foundation, University of Southern California, Los Angeles, 812 pp.","Holthe, T. (1986) Polychaeta Terebellomorpha. Marine Invertebrates of Scandinavia, 7, 1 - 192.","Hilbig, B. (2000) Family Ampharetidae Malmgren, 1866. In: Blake, J. A., Hilbig, B. & Scott, P. V. (Eds.), Taxonomic atlas of the benthic fauna of the Santa Maria Basin and Western Santa Barbara Channel. The Annelida Part 4. Polychaeta: Flabelligeridae to Sternaspidae. Santa Barbara Museum of Natural History, Santa Barbara, pp. 169 - 230.","Williams, S. J. (1987) Taxonomic notes on some Ampharetidae (Polychaeta) from Southern California. Bulletin of the Biological Society of Washington, 7, 251 - 258.","Day, J. H. (1973) New Polychaeta from Beaufort, with a key to all species recorded from North Carolina. NOAA Technical Reports, National Marine Fisheries Service, Circulars, 375, 1 - 140. http: // dx. doi. org / 10.5962 / bhl. title. 62852","Day, J. H. (1963) The Polychaete fauna of South Africa. Part 8: New species and records from grab samples and dredgings. Bulletin of the British Museum (Natural History), Zoology, 10 (7), 383 - 445."]}

Amage cf. ehlersi Reuscher, Fiege & Imajima, 2015 (Fig. 1 A–E) Specimens examined. SMF 24134, Yonaguni Knoll IV Hydrothermal Field, low CO2 seepage site, Okinawa Trough, 24°50.802’N 122°42.094’E, 1382 m, SO 196, Station 40, TV-MUC, 14 March 2008 (1 cs). Description. Length 3.5 mm, width 0.6 mm. Prostomium with middle lobe bearing anterolateral frontal horns (Fig. 1 A), delimited by incision from inflated surrounding lobe; prostomium without glandular ridges or eyes. Buccal tentacles smooth. Four pairs of cirriform branchiae in L-shaped arrangement in segments II–IV (Fig. 1 A), separated by wide median gap; innermost branchiae of anterior transverse row originating from segment II, outermost branchiae of anterior transverse row originating from segment III, median branchiae of longitudinal row originating from segment IV, posterior branchiae of longitudinal row originating from segment V. Segment II without chaetae. Notopodia with capillary chaetae from segment III, present in 14 chaetigers; anterior notopodia small, increasing in size from first to third pair; notopodial cirri absent (Fig. 1 A). Neuropodial tori with uncini from segment VI, present in 11 thoracic uncinigers; tori without cirri. Continuous ventral shields conspicuous to thoracic unciniger 11, faint to abdominal unciniger 4. Elevated or modified notopodia absent. Intermediate uncinigers absent. Eleven abdominal uncinigers with large digitiform rudimentary notopodia (Fig. 1 A). Pinnules with tuberculate dorsal cirrus. Rudimentary notopodia and pinnules connected by glandular stripe. Pygidium with crenulated terminal anus and one pair of short and thick lateral anal cirri (Fig. 1 A). Thoracic uncini in lower torus with 4 teeth in 1 row over basal prow and rostral tooth (Fig. 1 B), thoracic uncini in upper torus with one or two additional small teeth on top (Fig. 1 C). Abdominal uncini with about 7 teeth in two staggered rows over basal prow and rostral tooth (Fig. 1 D, E). Remarks. The single specimen collected at the Yonaguni Knoll IV Hydrothermal Field has eleven abdominal uncinigers, whereas Amage ehlersi Reuscher, Fiege & Imajima, 2015 was described with only ten. Otherwise the specimen agrees well with the original description. Future sampling effort in the Yonaguni Knoll IV Hydrothermal Field may help to conclude, if this vent population belongs to Amage ehlersi, or if the description of a new species is warranted. Distribution. Amage ehlersi has been found along the coast of Japan, in depths of 30–590 m (Reuscher et al. 2015). The finding at the Yonaguni Knoll Hydrothermal Field is the species’ second record and the first one from the vicinity of a hydrothermal vent. It is also the deepest and southernmost record of the species.

NAMANEREIS CHAMBERLIN, 1919 Namanereis Chamberlin, 1919: 196. See Glasby (1999) for full synonymy. Type species Lycastis quadraticeps Blanchard, 1849, by original designation. Straits of Magellan, Chile., Published as part of Glasby, Christopher J., Fiege, Dieter & Damme, Kay Van, 2014, Stygobiont polychaetes: notes on the morphology and the origins of groundwater Namanereis (Annelida: Nereididae: Namanereidinae), with a description of two new species, pp. 22-37 in Zoological Journal of the Linnean Society 171 (1) on page 24, DOI: 10.1111/zoj.12130, http://zenodo.org/record/5305715, {"references":["Chamberlin RV. 1919. The Annelida Polychaeta. Memoirs of the Museum of Comparative Zoology, Harvard College 48: 1 - 514.","Glasby CJ. 1999. The Namanereidinae (Polychaeta: Nereididae). Part 1. Taxonomy and phylogeny. Records of the Australian Museum Supplement 25: 1 - 129.","Blanchard E. 1849. Fauna Chilena. Anulares. P. C. Gay's Historia fisica y politica de Chile. Segun documentos adquiridos en esta republica durante doce anos de residencia en alla. Zoologia 3: 9 - 52. Paris."]}

Glasby, Christopher J., Fiege, Dieter, Damme, Kay Van (2014): Stygobiont polychaetes: notes on the morphology and the origins of groundwater Namanereis (Annelida: Nereididae: Namanereidinae), with a description of two new species. Zoological Journal of the Linnean Society 171 (1): 22-37, DOI: 10.1111/zoj.12130, URL: http://dx.doi.org/10.1111/zoj.12130

Terebellides mediterranea spec. nov. (Figures 5���8, 12 a, d, e, 13; Table 1) Material examined. A total of 10 specimens were examined (11.9% of the total Terebellides specimens collected). Type material: Station SJ 0 0 5 - 30.08. 2004 (PMR- 14558, 2 paratypes). Station SJ 0 0 7 - 27.02. 2003 (PMR- 14559, 1 holotype; PMR- 14560, 1 paratype on SEM stub); 28.05. 2003 (PMR- 14561, 1 paratype; PMR- 14562, 1 paratype on SEM stub); 29.01. 2004 (MNCN 16.01/ 14716, 1 paratype). Non-type material: Station SJ 0 0 5 - 27.02. 2003 (1 spec.) (coll. BM). SJ 0 0 5 - 30.08. 2004 (2 specs.) (coll. BM). Comparative material: Terebellides californica Williams, 1984. Paratype AM W 197111. Type specimens of T. californica were requested to the Los Angeles California Natural History Museum, but unfortunately they were not available for study. However, general characteristics of this species presented in Hutchings and Peart (2000) and Sch��ller and Hutchings (2010) were corroborated by P. Hutchings who kindly checked the paratype of this species deposited in the Australian Museum (Sydney) (AM). Description based on holotype. Complete specimen, 23 mm long and 2.0 mm wide; body tapering posteriorly with segments increasingly shorter and crowded towards pygidium. Prostomium compact; large tentacular membrane surrounding the mouth provided with many long buccal tentacles with expanded tips (Fig. 5 a, 8 a). SGI forming an expanded structure below tentacular membrane. Lateral lappets on SGIII���VII, CH 1���5, being larger and continuing ventrally in SGIII���V declining in size posteriorly (Fig. 5 a). No conspicuous dorsal rounded projection on anterior chaetigers or oval-shaped glandular region in CH 3. Branchiae arising as single structure from SGIII, consisting of a single stalked structure situated mid-dorsally (Fig. 5 a) made up of two pairs of lobes fused along most of their lengths; lower pair much shorter then upper pair. Pointed projection of posterior region of both upper and lower lobes and large anterior branchial projection (fifth lobe) present (Fig. 5 b). Both sides of branchial lamellae provided with several parallel bent rows of cilia (Fig. 6 a) and tufts of cilia on the outer edge (Fig. 6 b). Eighteen pairs of thoracic notopodia (SGIII ���XX). Notopodia present from CH 1, larger than subsequent notopodia (Fig. 5 a, c, d); notochaetae of CH 1 much longer than following notochaetae. All notochaetae simple capillaries with textured surface (Fig. 6 c). Neuropodia present as sessile pinnules from CH 6 (SGVIII) to pygidium and provided with uncini in single rows starting from CH 7 (SGIX) throughout. First thoracic neuropodia (CH 6) provided with 4���5 sharply bent, acute tipped, geniculate acicular hooks (Fig. 6 d). Minute teeth forming a capitium on geniculate chaetae not observed. Second and all subsequent thoracic neuropodia with up to 10���16 uncini per torus (Fig. 7 a). Uncini provided with long shafted denticulate hooks with 3���4 teeth above main fang surmounted by 6���7 shorter teeth and an upper crest of several smaller denticles (Fig. 7 b), dental formula MF: 3���4: 6���7:���. Thirty-two abdominal neuropodia as erect pinnules provided with about 33 uncini per torus (Fig. 7 c); uncini with four teeth above main fang surmounted by a fifth tooth in the middle, an upper crest of 4 teeth (Fig. 7 d) and a variable number of smaller teeth, dental formula MF: 4: 1: 4:���. One large papilla located behind first thoracic notopodia (Figs 5 d; 8 b), and two button-hole like pairs of nephridial openings; located dorsal to each notopodium of SGVI and VII (CH 4 and 5) (Fig. 8 c, d). Pygidium blunt, funnel-like depression. MG staining pattern 1 (Figs 12 a,d,e; 13 a): compact green colouration in CH 1 ��� 3, then turning into striped pattern in CH 4 ��� 12 and fading in the following segments. Colour in alcohol pale brown (Fig. 13 b). Remarks. The presence of large notopodia provided with long notochaetae in the first thoracic chaetiger is a character usually employed to discriminate species in taxonomic keys of the genus Terebellides (Garraffoni & Lana 2003; Solis-Weiss et al. 2009) and also in phylogenetic studies (Garraffoni & Lana 2004). Following Hutchings and Peart (2000) two species have this diagnostic character: T. kobei Hessle, 1917 and T. californica Williams, 1984. Terebellides kobei was described by Hessle (1917) from specimens collected in Kobe Bay (Japan), later reported from the same area by Imajima and Hartman (1964) and described in more detail by Imajima and Williams (1985). Surprisingly, this work ignores the record of Williams (1984) in the Indian Ocean (Mozambique Channel) probably due to simultaneous date of publication. Our specimens clearly differ from T. kobei in having notopodia and notochaetae of CH 1 much longer (similar to Williams��� material), by the absence of a conspicuous triangular lobe and a glandular area at the level of notopodia of CH 3 (Table 1) and by the similar length and high degree of fusion of posterior branchial lobes (see also Hutchings & Peart 2000, Table 3 A). Terebellides californica was described by Williams (1984) from the Pacific Ocean (Oregon to Western Mexico) at shelf and slope depths, and later reported from the same area by Hern��ndez-Alc��ntara and Sol��s-Weiss (1999) and Hilbig (2000). Hern��ndez-Alc��ntara and Sol��s-Weiss (1998) report T. californica for the Mexican Caribbean but we suspect that this may correspond to other species with large CH 1 as well. Williams (1984) characterized the taxon only by the ���very well developed first chaetiger with greatly prolonged fine notosetae��� (Williams 1984, p. 128). The species was later redescribed by Hilbig (2000) proposing a ���trilobed structure of the peristomium��� as potential new diagnostic character. This character was not observed in our specimens, but in our opinion its relevance should be taken with caution as its presence in the species has not been sufficiently assessed. Terebellides mediterranea spec. nov., differs from T. californica in branchial structure in addition to their very different geographical location���shelf and slope depths of the Pacific Ocean in T. californica vs. shallow waters in the Adriatic Sea in T. mediterranea spec. nov. In this sense, in T. mediterranea spec. nov., a large fifth branchial lobe is present and posterior pairs of lobes (first to fourth lobes) are fused along most of their lengths while T. californica lacks a fifth branchial lobe and posterior pairs of lobes are moderately fused (Hutchings & Peart 2000; Sch��ller & Hutchings 2010). Habitat. Offshore stations in the northern Adriatic Sea on silty sand bottom on 31 m depth. Known only from type locality. Distribution. Adriatic Sea. Etymology. The name of the species refers to the Mediterranean Sea., Published as part of Parapar, Julio, Mikac, Barbara & Fiege, Dieter, 2013, Diversity of the genus Terebellides (Polychaeta: Trichobranchidae) in the Adriatic Sea with the description of a new species, pp. 333-350 in Zootaxa 3691 (3) on pages 338-342, DOI: 10.11646/zootaxa.3691.3.3, http://zenodo.org/record/248600

Terebellides stroemii Sars, 1835 (Figures 9���11, 12 c, 13) Terebellides stroemii Sars, 1835: 48 ���50, Pl. 12 (labelled 13), Fig. 31 a���e. Terebellides stroemii ���Garraffoni et al. 2005: 14. Garraffoni & Lana 2003: 356. Garraffoni & Lana 2004: 973, Tables 1���2, Figs 5���6. Jirkov 2001: 529, Figs 1���5. Parapar et al. (2011): 14, Figs 11, 12, 13 d. Terebellides stroemi ���Williams 1984: 119, Figs 1 a���c, 3, 6. Imajima & Williams 1985: 11. Holthe 1986 a: 170. Sol��s-Weiss et al. 1991: 147. Bremec & El��as 1999: 177. non Terebellides stroemii ���Hutchings & Peart 2000: 254, Figs. 13 f, 16, Tab. 3. Material examined. A total of 51 specimens were examined (60.7% of the total Terebellides specimens collected) in all four stations studied. Station SJ 0 0 5: 28.05. 2003 (PMR- 14563, 1 spec.; PMR- 14564, 1 spec.); 0 7.06.0 4 (PMR- 14565, 1 spec.); 0 2.12. 2004 (PMR- 14566, 1 spec.; PMR- 14567, 2 specs.). Station SJ 0 0 7: 27.02. 2003 (4 specs.) (coll. BM); 28.05. 2003 (PMR- 14568, 4 specs.); 12.08. 2003 (MNCN 16.01/ 14717, 2 specs.; MNCN 16.01/ 14718, 1 spec.); 29.01.0 4 (PMR- 14569, 2 specs.); 30.08.0 4 (PMR- 14570, 1 spec.). Station LIM K 2: 0 7.07. 2010 (PMR- 14571, 10 specs.); 0 7.07. 2010 (10 specs.) (coll. BM). Station LIM K 5: 0 7.07. 2010 (PMR- 14572, 9 specs.; PMR- 14573, 2 specs. on one SEM stub). Description of Adriatic Sea specimens. Complete specimens ranging from 25 to 34 mm in length and 3.0 to 2.0 mm in width; specimens from LIM stations much larger than ones from SJ stations; body tapering posteriorly with segments becoming increasingly shorter and compact towards pygidium. Prostomium compact; tentacular membrane surrounding mouth and provided with buccal tentacles with expanded tips. First segment forming an expanded structure below tentacular membrane. Lateral lappets on SGIII���IX (CH 1���7) (Fig. 9 a, b). Some specimens with more or less conspicuous dorsal rounded projection in CH 4 ��� 6. An oval-shaped glandular region could be seen in lateral part of thoracic CH 3 (Fig. 9 a, b). Branchiae arising as single structure from segment 3 consisting of a single stalked structure located middorsally made up of two pairs of posterior lobes fused along most of their length; lower pair of same length but thinner than upper pair (Fig. 9 b). Pointed projection of posterior region of lobes present in both lobes. Anterior branchial projection (fifth lobe) present. Branchiae provided with papillar projections pointing over the edge of the branchial lamellae, the latter also provided with several parallel bent rows of cilia on both sides (Fig. 9 c���d). Eighteen pairs of thoracic notopodia (SGIII ���XX). Notopodia and notochaetae of CH 1 shorter in size to subsequent notopodia. Neuropodia present as sessile pinnules from CH 6 (SGVIII) to pygidium and provided with uncini in single rows throughout. First thoracic neuropodia (CH 6) with 4���5 sharply bent, acute tipped, geniculate acicular hooks (Fig. 10 a). Minute teeth forming a capitium on geniculate chaetae not observed (Fig. 10 b). Second and all subsequent thoracic neuropodia with up to 10���16 uncini per torus. Uncini provided with long shafted denticulate hooks with 2���4 teeth above main fang surmounted by about 3 shorter teeth and an upper crest of several smaller denticles (Fig. 10 c, d), dental formula MF: 2���4: 3:���. Between 30���32 abdominal neuropodia as erect pinnules provided with about 23 uncini per torus; uncini with 4 teeth above main fang surmounted by an upper crest of 3���5 shorter teeth and a variable number of smaller teeth (Fig. 11 a), dental formula MF: 4: 3���5:���. One large, button-hole like nephridial opening on each notopodium of CH 4���5 (Fig. 11 b). Low ciliated papillae located dorsally to all thoracic notopodia from second chaetiger (Fig. 11 c, d). Pygidium blunt, funnel-like depression. MG staining pattern 5 (Fig. 12 c; 13 a): compact green colouration in CH 1���3, after turning into striped pattern in CH 4���12 and fading in following segments. Oval-shaped glandular region of CH 3 also stained but differently to others. Colour in alcohol pale brown (Fig. 13 b), oval region of CH 3 slightly lighter. Remarks. General characteristics of Adriatic specimens agree with those of Icelandic specimens identified as T. stroemii sensu Holthe (1986 a) by Parapar et al. (2011), and therefore differ from those characters referred to this species by Hutchings and Peart (2000) from the study of some Norwegian specimens: presence and degree of development of the anterior lateral lappets, position of nephridial openings and shape of geniculate chaetae. Other characters also in agreement with Parapar et al. (2011) are the MG coloration pattern and the distribution of branchial ciliature. Habitat. The species was reported in a wide range of depths and temperatures in all world oceans, nevertheless, it is impossible to establish with confidence any habitat preferences given that today, it is considered a complex of species. Terebellides stroemii was frequently reported in all parts of the Adriatic Sea on soft bottoms up to a depth of 1,150 m and was considered a species of wide ecological distribution. In this research the species was found in the northern Adriatic Sea on offshore stations on silty sand bottom at 31 m depth and on coastal stations on muddy bottom at 28���29 m depth. Distribution. Boreo-Arctic waters (Hutchings & Peart 2000). Our record in the Adriatic Sea confirms the presence of T. stroemii in Mediterranean waters., Published as part of Parapar, Julio, Mikac, Barbara & Fiege, Dieter, 2013, Diversity of the genus Terebellides (Polychaeta: Trichobranchidae) in the Adriatic Sea with the description of a new species, pp. 333-350 in Zootaxa 3691 (3) on pages 342-344, DOI: 10.11646/zootaxa.3691.3.3, http://zenodo.org/record/248600

Sosane brevibranchiata sp. nov. (Figs. 7 A���J; 16 D) Specimens examined. Holotype: NSMT-Pol. H 564, Bungo Channel, 32 ��43.0'N, 132 �� 32.3 'E ��� 32 �� 42.9 ���N, 132 ��32.0'E, 84���99 m, KT 99 - 18, St. DG- 1, 12.1999, (1 cs). Paratype: NSMT-Pol P 565, Off Tsushima Island, 34 �� 15.1 'N, 130 ��15.0'E ��� 34 ��15.0'N, 130 �� 14.9 'E, 100 m, Soyo-maru, SO 08-D 5, 7.2008, (1 af). Description. Length 10 mm, width 1 mm. Prostomium without glandular ridges, with one pair of eyespots (Fig. 7 A). Buccal tentacles without groove, smooth. Lower lip slightly crenulated (Fig. 7 B). Four pairs of cirriform branchiae (Fig. 7 C); 3 pairs of branchiae in transverse row in segment II, 1 pair of branchiae in segment IV; branchial groups separated by wide median gap; branchiae of segment II in median position of transverse row, branchiae of segment III in outermost position of transverse row, branchiae of segment IV in innermost position of transverse row, branchiae of segment V emerging next to notopodia of segment IV (Fig. 16 D); branchiae of transverse row with ventral tufts of cilia, annulated (Fig. 7 D); posterior branchiae much shorter, without cilia. Chaetae in segment II of same length and thickness as following notochaetae (Fig. 7 B, C). Notopodia with limbate capillary notochaetae from segment III, present in 15 segments. Notopodia in third-to-last thoracic unciniger elevated, basally inflated, apically conical, not connected by dorsal ridge (Fig. 7 E, F); notochaetae of modified unciniger in fan-like arrangement on convex side of notopodia, with hirsute tips (Fig. 7 G). Neuropodial tori with uncini from segment VI, present in 12 thoracic uncinigers. Cirri and papillae in thoracic parapodia absent. Continuous ventral shields present to thoracic unciniger 10. Two intermediate uncinigers. Ten abdominal uncinigers. Rudimentary notopodia and glandular pads in intermediate and abdominal uncinigers absent. Pinnules without cirri or papillae. Pygidium with terminal anus and one pair of short ventrolateral digitiform anal cirri (Fig. 7 H). Thoracic and abdominal uncini with crest of numerous teeth above rostral tooth and basal prow (Fig. 7 I, J). Remarks. Sosane brevibranchiata sp. nov. differs from the other species of Sosane sensu stricto, S. jirkovi, S. occidentalis, and S. sulcata, by the rudimentary 4 th pair of branchiae and the large gap between the groups of branchiae. The ventral tufts of cilia in the first 3 pairs of branchiae and their distinct annulation have also been observed in other species of the genus Sosane, i.e., Sosane uebelackerae sp. nov. (see below), and other genera, e.g., Anobothrus (see above). The ciliation is probably a juvenile character. Distribution. Bungo Channel between Kyushu and Shikoku, and off Tsushima Island in the Korea Strait, in 84��� 100m., Published as part of Imajima, Minoru, Reuscher, Michael G. & Fiege, Dieter, 2013, Ampharetidae (Annelida: Polychaeta) from Japan. Part II: Genera with elevated and modified notopodia, pp. 137-166 in Zootaxa 3647 (1) on pages 149-150, DOI: 10.11646/zootaxa.3647.1.7, http://zenodo.org/record/224273

Sosane wireni (Hessle, 1917) (Figs. 12 A���G; 17 C) Specimens examined. Moroiso Bay, 35 ��09.4'N, 139 �� 36.8 'E, 30 m, St. 2, 3.1979 (1 cs). Off Shimoda, 34 �� 38.4 'N, 138 �� 56.3 'E ��� 34 �� 38.5 'N, 138 �� 56.5 'E, 37���39 m, St. 12, 9.1987 (1 cs). Kushimoto, 33 �� 27.2 'N, 135 �� 45.4 'E ��� 33 �� 27.2 'N, 135 �� 45.6 'E, 19���27 m, St. 14, 7.1978 (3 cs); 33 �� 29.1 'N, 135 ��51.0'E ��� 33 �� 29.2 'N, 135 �� 51.2 'E, 34 m, St. 9, 7.1978 (1 cs); 33 �� 27.4 'N, 135 �� 44.2 'E ��� 33 �� 27.3 'N, 135 ��44.0'E, 43���48 m, St. 15, 7.1978 (2 cs). Description. Length 5 to 8 mm, width 0.8 to 1 mm. Prostomium with middle lobe delimited by incision, without glandular ridges or eyes (Fig. 12 A, B). Buccal tentacles unknown. Lower lip not crenulated. Four pairs of cirriform branchiae (Fig. 12 A); 3 pairs of branchiae in triangular arrangement in segment II, and 1 pair in segment IV; branchial groups separated by median gap of more than one branchial width; branchiae of segment II inserted in anteromedian position of triangle, branchiae of segment III in outermost position of triangle, branchiae of segment IV in innermost position of triangle, branchiae of segment V emerging next to notopodia of segment IV (Fig. 17 C); branchiae in smallest specimen ciliated, without cilia in bigger specimens. Chaetae in segment II absent. Notopodia with limbate capillary notochaetae from segment III, present in 15 segments (Fig. 12 C). Notopodia in third-to-last thoracic unciniger elevated, basally inflated, apically bifid, not connected by dorsal ridge (Fig. 12 D, E); notochaetae of modified unciniger in fan-like arrangement on convex side of notopodia, with indistinctly hirsute tips (Fig. 12 F). Neuropodial tori with uncini from segment VI, present in 12 thoracic uncinigers. Cirri and papillae in thoracic parapodia absent. Continuous ventral shields present to thoracic unciniger 8 or 9. Two intermediate uncinigers. Nine abdominal uncinigers. Rudimentary notopodia and glandular pads in intermediate and abdominal uncinigers absent. Pinnules without cirri or papillae. Pygidium with terminal anus and 1 pair of ventrolateral cirriform anal cirri. Thoracic and abdominal uncini with crest of numerous teeth above rostral tooth and basal prow (Fig. 12 G). Remarks. There are two different species, Sosane wireni (Hessle, 1917) (described as Sosanopsis wireni) and Sosane wireni Caullery, 1944. The synonymy of Sosane and Sosanopsis would leave S. wireni Caullery, 1944 as homonym of Hessle���s species. However, Caullery���s species description of S. wireni and S. fauveli Caullery, 1944 seem to be based on a misconception of the genus Sosane since both of Caullery���s species do not have the characteristically modified segment. We think that Caullery���s species may belong to Lysippe. A re-examination of Caullery���s material was not possible because collections were being moved between the natural history museums of Amsterdam and Leiden during the time of this study. Distribution. North Sea, Barents Sea, Laptev Sea (Holthe 1986 a, Hartmann-Schr��der 1996), New England (Hilbig 1994), California (Hilbig 2000). Newly recorded from Sagami Bay and Kushimoto, Pacific coast of Honshu, in 19��� 48 m., Published as part of Imajima, Minoru, Reuscher, Michael G. & Fiege, Dieter, 2013, Ampharetidae (Annelida: Polychaeta) from Japan. Part II: Genera with elevated and modified notopodia, pp. 137-166 in Zootaxa 3647 (1) on pages 156-157, DOI: 10.11646/zootaxa.3647.1.7, http://zenodo.org/record/224273

Genus Terebellides Sars, emended by Sch��ller and Hutchings 2013 Type species: Terebellides stroemii Sars, 1835 Diagnosis. Trichobranchidae with compact prostomium fused to free frontal edge of the peristomium. Peristomium forming lips, upper lip typically hidden, lower lip expanded. Branchial stems fused, branchiae forming single, lamellate structure on mid-dorsum, made up of 1 to 4 lobes, sometimes an anterior prolongation of lobes (fifth lobe) present. Eyespots absent. Lateral lobes absent. Thorax with 18 pairs of notopodia from segment III and neuropodia from segments VII (chaetiger 5) or segment VIII (chaetiger 6) to pygidium. Notochaetae all capillaries with varying degrees of ornamentation. First, and sometimes second thoracic neuropodia with smooth, geniculate hooks, subsequent thoracic ones with denticulate hooks. Abdominal uncini avicular. Remarks. Parapar et al. (2011) found minute teeth forming a capitium on geniculate chaetae in all Icelandic species (T. stroemii Sars, 1835, T. gracilis Malm, 1874, T. atlantis Williams, 1984 and T. bigeniculatus Parapar, Moreira and Helgason, 2011). We consider the characterisation of geniculate chaetae as ���smooth��� in the current diagnosis as doubtful., Published as part of Parapar, Julio, Mikac, Barbara & Fiege, Dieter, 2013, Diversity of the genus Terebellides (Polychaeta: Trichobranchidae) in the Adriatic Sea with the description of a new species, pp. 333-350 in Zootaxa 3691 (3) on pages 334-335, DOI: 10.11646/zootaxa.3691.3.3, http://zenodo.org/record/248600

Family Trichobranchidae Malmgren, 1866, Published as part of Parapar, Julio, Mikac, Barbara & Fiege, Dieter, 2013, Diversity of the genus Terebellides (Polychaeta: Trichobranchidae) in the Adriatic Sea with the description of a new species, pp. 333-350 in Zootaxa 3691 (3) on page 334, DOI: 10.11646/zootaxa.3691.3.3, http://zenodo.org/record/248600

Zatsepinia Jirkov, 1986 Type species: Zatsepinia rittichae Jirkov, 1986 Generic diagnosis (emended). Prostomium simple, without glandular ridges. Buccal tentacles smooth. Two or three pairs of cirriform branchiae. Notochaetae in segments II and III absent. Ten thoracic uncinigers. Notopodial cirri absent. Second-to-last thoracic unciniger with elevated notopodia, connected by mid-dorsal ridge. Four intermediate segments. Abdominal rudimentary notopodia absent. Remarks. The generic diagnosis has been emended to account for the presence of 3 pairs of branchiae, found in Zatsepinia jirkovi sp. nov., and the number of intermediate uncinigers., Published as part of Imajima, Minoru, Reuscher, Michael G. & Fiege, Dieter, 2013, Ampharetidae (Annelida: Polychaeta) from Japan. Part II: Genera with elevated and modified notopodia, pp. 137-166 in Zootaxa 3647 (1) on page 160, DOI: 10.11646/zootaxa.3647.1.7, http://zenodo.org/record/224273

Anobothrus dayi sp. nov. (Figs. 4 A���J; 16 A) Specimens examined. Holotype: NSMT-Pol. H 551, Yakiuchi Bay, Amami-Oshima Island, 28 �� 16.4 'N, 129 �� 16.5 'E ��� 28 �� 16.5 'N, 129 �� 16.6 'E, 47 ��� 45 m, St. 15, 7.1989. Paratype: NSMT-Pol. P 552, same locality as holotype (15 cs, 3 af). Paratypes: Yakiuchi Bay, NSMT-Pol. P 566, 28�� 16.6 'N, 129 �� 17.2 'E ��� 28 �� 16.6 'N, 129 �� 17.4 'E, 38 ��� 30 m, St. 16, 7.1989 (6 cs); NSMT-Pol. P 567, 28�� 16.1 'N, 129 �� 16.2 'E ��� 28 �� 16.1 'N, 129 �� 16.4 'E, 53 ��� 49 m, St. 14, 7.1989 (1 cs); SMF 21690, 28�� 16.4 'N, 129 �� 13.9 'E ��� 28 �� 16.4 'N, 129 �� 14.1 'E, 63���71 m, St. 11, 7.1989 (7 cs). Additional specimens: Off Shimoda, 34 ��41.0'N, 139 ��00.8'E ��� 34 �� 40.4 'N, 139 ��02.5'E, 106 ��� 97 m, St. 26, 11.1981 (1 af). Tosa Bay, 33 �� 26.7 'N, 133 �� 34.8 'E, 46 m, No. 2 - 2, 4.1970 (1 cs). West of Cape Ashizuri, 32 �� 44.3 'N, 132 �� 41.1 'E ��� 32 �� 44.4 'N, 132 �� 40.8 'E, 124���125 m, KT- 99 - 18, St. DG- 8, 12.1999 (8 cs). Description. Length 7 mm, width 0.6 mm. Prostomium with conical middle lobe delimited by incision, without glandular ridges or eyes (Fig. 4 A, B). Buccal tentacles with ventral groove, smooth. Three pairs of cirriform branchiae in fused segment II + III (Fig. 4 C), arranged in transverse row; groups of branchiae separated by wide median gap; segmental origin of outermost and median branchiae not determinable; branchiae of segment IV inserted in innermost position of transverse row (Fig. 16 A). Chaetae in fused segments II + III originating from segment II, longer and slightly thicker than following capillaries, pointing forwards (Fig. 4 B, C, D). Chaetae of segment III absent. Notopodia with limbate capillary notochaetae from segment IV, present in 14 segments. Notopodia in fifth-to-last thoracic unciniger elevated, connected by dorsal ridge (Fig. 4 E); notochaetae of modified notopodia with broad wings and hirsute tip (Fig. 4 F). Neuropodial tori with uncini from segment VI, present in 12 thoracic uncinigers. Cirri and papillae in thoracic parapodia absent. Circular glandular band absent. Continuous ventral shields present to thoracic unciniger 9. Two intermediate uncinigers. Ten abdominal uncinigers. Rudimentary notopodia and glandular pads in intermediate and abdominal uncinigers absent. Pinnules without cirri or papillae. Pygidium with terminal anus and one pair of ventrolateral cirriform anal cirri (Fig. 4 G). Nephridial papillae absent. Thoracic uncini with 11 teeth in 2 alternating rows above rostral tooth and basal prow (Fig. 4 H, I). Abdominal uncini with crest of numerous teeth above rostral tooth and basal prow. Remarks. No cilia are visible in the branchiae of the holotype and the larger paratypes. The smaller paratypes have branchiae with ventral tufts of cilia (Fig. 4 J). The smallest (non-type) specimens have branchiae without cilia. The development of a dorsal ridge between the elevated notopodia differs among specimens. Larger specimens usually have a more pronounced dorsal ridge. The only other species in the genus with 3 pairs of branchiae are Anobothrus laubieri (Desbruy��res, 1978) and Anobothrus flabelligerulus sp. nov. Anobothrus dayi sp. nov. differs from these species by the conical shape of the prostomium and the wide gap between the groups of branchiae. Further differences include the chaetae of segment II (paleae), which are much thinner than those of A. flabelligerulus sp. nov., and the notochaetae of segment III, which are absent in A. dayi sp. nov. and A. flabelligerulus sp. nov. but present in A. laubieri. Etymology. The species is named after John Hemsworth Day, in recognition of his extensive research on the taxonomy of ampharetid polychaetes. Distribution. Northwest Pacific, Japan, Sagami Bay and Tosa Bay, Pacific coast of Honshu, and Yakiuchi Bay, East China Sea coast of Amami-Oshima Island, in 30��� 125 m., Published as part of Imajima, Minoru, Reuscher, Michael G. & Fiege, Dieter, 2013, Ampharetidae (Annelida: Polychaeta) from Japan. Part II: Genera with elevated and modified notopodia, pp. 137-166 in Zootaxa 3647 (1) on pages 144-145, DOI: 10.11646/zootaxa.3647.1.7, http://zenodo.org/record/224273

Sosane cf. cinctus (Hartman, 1965) (Fig. 8 A���C) Muggoides cinctus Hartman, 1965: 221 ���222, pl. 48, figs. c���e Mugga cinctus: Jirkov 1994 b: 35. Sosane cinctus: Jirkov 2001: 486; Jirkov 2008: 114, tab. 1 Specimens examined. North of Tokunoshima Island, 28 ��03.79'N, 128 �� 56.31 'E ��� 28 ��04.71'N, 128 �� 57.59 'E, 533��� 583 m, KH-05- 1, St.OT- 10, 5.2005 (1 cs). Additional material examined. Melinnata americana Hartman, 1965 Holotype: LACM-AHF POLY 246. North Atlantic, USA, New England continental slope, 36 �� 23 ��� 30 ���N, 68 ��04��� 30 ���W, 4850 m, anchor dredge, R/V Atlantis, Sta. KK 1, coll. Sanders, H., Woods Hole Oceanographic Institution, 10 Aug. 1961. Paratype: LACM-AHF POLY 247. Collected at same station as holotype. Muggoides cinctus Hartman, 1965 Holotype: LACM-AHF POLY 242. North Atlantic, Bermuda, Bermuda slope, 32 �� 17 ���00���N, 64 �� 35 ���W, 1700 m, R/V Atlantis, Sta. Bermuda 4, 2 May 1960. Paratype: LACM-AHF POLY 243. Collected at same station as holotype. Description. Length 3.4 mm, width 0.4 mm. Prostomium with middle lobe delimited by incision, without glandular ridges or eyes (Fig. 8 A). Buccal tentacles unknown. Lower lip crenulated (Fig. 8 A). Branchiae lost; scars in segment II visible, but exact number and position of branchiae indeterminable. Fused segments II + III with 1 pair of thin capillary notochaetae, notopodia reduced (Fig. 8 A). Notopodia with capillary notochaetae from segment IV, first 2 pairs reduced in size. 14 thoracic chaetigers. Notopodia in last thoracic unciniger elevated, basally inflated, with terminal conical lobe, connected by dorsal ridge (Fig. 8 B); notochaetae of modified unciniger in fan-like arrangement on convex side of notopodia, with hirsute tips (Fig. 8 C). Neuropodial tori with uncini from segment VI, present in 11 thoracic uncinigers. Cirri and papillae in thoracic parapodia absent. Continuous ventral shields distinct to thoracic unciniger 8, faint to thoracic unciniger 11. Two intermediate uncinigers. Eight abdominal uncinigers. Rudimentary notopodia and glandular pads in intermediate and abdominal uncinigers absent. Pinnules without cirri or papillae. Pygidium with terminal anus and 1 pair of lateral blunt lobes. Thoracic and abdominal uncini with crest of numerous teeth above rostral tooth and basal prow. Remarks. During the examination of holo- and paratypes of Sosane cinctus (Hartman, 1965) we found that the species has 4, rather than 3 pairs of branchiae. The number of branchiae is, even with methyl green staining, indeterminable in specimens where branchiae are broken off, e.g. in the holotype. Several paratype specimens, however, have a complete set of 4 pairs of branchiae. Numbers of thoracic chaetigers and uncinigers are 14 and 11, respectively, which is in contrast to the 13 thoracic chaetigers and 10 thoracic uncinigers given in the original description. In our single specimen all branchiae are broken off. We were not able to determine the number of branchiae. All other characters, however, agree with those observed in S. cinctus. Distribution. The species has only been recorded from its type locality Bermuda. Records (as Muggoides) with uncertain species affiliation exist from Cape Hatteras off the coast of North Carolina as Muggoides nr. cinctus (Hilbig 1994) and from the Southern Ocean as Muggoides cf. cinctus (Sch��ller & Ebbe 2007) and Muggoides sp. 1 (Hilbig 2004; Brandt et al. 2007), respectively. Newly recorded from the East China Sea., Published as part of Imajima, Minoru, Reuscher, Michael G. & Fiege, Dieter, 2013, Ampharetidae (Annelida: Polychaeta) from Japan. Part II: Genera with elevated and modified notopodia, pp. 137-166 in Zootaxa 3647 (1) on pages 150-151, DOI: 10.11646/zootaxa.3647.1.7, http://zenodo.org/record/224273

Sosane trigintaduo sp. nov. (Figs. 10 A���H; 17 A) Specimens examined. Holotype: NSMT-Pol. H 564, Bungo Channel, 32 ��43.0'N, 132 �� 32.3 'E ��� 32 �� 42.9 ���N, 132 ��32.0'E, 84���99 m, KT 99 - 18, St. DG- 1, 12.1999, (1 cs). Paratype: NSMT-Pol P 565, Off Tsushima Island, 34 �� 15.1 'N, 130 ��15.0'E ��� 34 ��15.0'N, 130 �� 14.9 'E, 100 m, Soyo-maru, SO 08-D 5, 7.2008, (1 af). Description. Length 9 mm, width 1 mm. Prostomium with middle lobe delimited by incision, without glandular ridges or eyes (Fig. 10 A, B, C). Buccal tentacles without groove, smooth. Lower lip crenulated (Fig. 10 B). Four pairs of cirriform branchiae (Fig. 10 A); three pairs of branchiae in transverse row in segment II, 1 pair of branchiae in segment IV; branchial groups separated by wide median gap; branchiae of segment II in 2 nd outermost position of transverse row, branchiae of segment III in outermost position of transverse row, branchiae of segment IV in innermost position of transverse row, branchiae of segment V emerging next to notopodia of segment IV (Fig. 17 A). Chaetae in segment II absent. Notopodia with limbate capillary notochaetae from segment III, present in 16 segments. Notopodia in fourth-to-last thoracic unciniger elevated, basally inflated, apically conical, not connected by dorsal ridge (Fig. 10 D, E); notochaetae of modified unciniger in fan-like arrangement on convex side of notopodia, with hirsute tips (Fig. 10 F). Neuropodial tori with uncini from segment VI, present in 13 thoracic uncinigers. Cirri and papillae in thoracic parapodia absent. Last segment of continuous ventral shields indeterminable. One intermediate unciniger. Eight abdominal uncinigers. Rudimentary notopodia and glandular pads in intermediate and abdominal uncinigers absent. Pinnules without cirri or papillae. Pygidium with terminal anus and one pair of short ventrolateral cirriform anal cirri (Fig. 10 G). Thoracic and abdominal uncini with crest of numerous teeth above rostral tooth and basal prow (Fig. 10 H). Remarks. Sosane trigintaduo sp. nov. is the first species of the genus with 13 thoracic uncinigers and the modification located in the fourth-to-last thoracic unciniger. We consider Sosane trigintaduo sp. nov. the possible link between the genus Lysippe and the remaining Sosane species, as discussed in the phylogenetic analysis. Etymology. The species name ��� trigintaduo ��� is Latin for thirty-two, which refers to the 32 notopodia (16 pairs)���a unique character state in the genus Sosane. Distribution. Sagami Bay, Pacific coast of central Honshu, in ca. 100 m., Published as part of Imajima, Minoru, Reuscher, Michael G. & Fiege, Dieter, 2013, Ampharetidae (Annelida: Polychaeta) from Japan. Part II: Genera with elevated and modified notopodia, pp. 137-166 in Zootaxa 3647 (1) on page 153, DOI: 10.11646/zootaxa.3647.1.7, http://zenodo.org/record/224273