Ophryotrocha geoffreadi, sp. nov.

Ophryotrocha geoffreadi sp. nov. urn:lsid:zoobank.org:act: F5023AAF-791B-47A3-90A2-824D50CC4826 Fig. 7 Etymology The species is named after Dr Geoffrey Read, the chief taxonomic editor of Polychaeta at the World Register of Marine species (WoRMS) and founder of the Annelida mailing list. His tireles...

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Main Authors: Ravara, Ascensão, Wiklund, Helena, Cunha, Marina R.
Format: Text
Language:unknown
Published: Zenodo 2021
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Online Access:https://dx.doi.org/10.5281/zenodo.4570311
https://zenodo.org/record/4570311
Description
Summary:Ophryotrocha geoffreadi sp. nov. urn:lsid:zoobank.org:act: F5023AAF-791B-47A3-90A2-824D50CC4826 Fig. 7 Etymology The species is named after Dr Geoffrey Read, the chief taxonomic editor of Polychaeta at the World Register of Marine species (WoRMS) and founder of the Annelida mailing list. His tireless work in both these initiatives is an immense and invaluable aid to all polychaetologists. Material examined Holotype MOROCCO • complete spec. (ethanol), 0.94 mm long, 0.17 mm wide, 16 chaetigers; GoC, Meknès MV; 34°59.091′ N, 07°04.424′ W; 698 m depth; 20 May 2009; Stn B09-14b_03W; wood substrata; NHMUK 2020.1512. Paratypes MOROCCO • 31 specs (formalin); same collection data as for holotype; NHMUK 2020.1513 • 1 spec. (ethanol), 2 specs (slide preparation); same collection data as for holotype; DBUA0002286.02. Other material MOROCCO • 5 specs (ethanol); same locality as for holotype; 20 May 2009; Stn B09-14b_03A; alfalfa substrata; DBUA0002286.03 (1 hologenophore, 4 paragenophores) • 2 specs (ethanol), 13 specs (formalin); GoC Darwin MV; 35°23.523′ N, 07°11.513′ W; 1100 m depth; 19 May 2009; Stn B09- 14b_02A; alfalfa substrata; DBUA0002286.04 • 9 specs (ethanol), 1 spec. (slide preparation), 5 specs (formalin); same collection data as for preceding; 19 May 2009; Stn B09-14b_02W; wood substrata; DBUA0002286.05. Description Relatively small specimens compared to most species of Ophryotrocha . Most of the larger specimens are damaged or incomplete and were not measured. Measured specimens 0.73 to 1.46 mm long and 0.19 mm wide, for 17 to 25 chaetigers (Fig. 3). Body dorso-ventrally flattened, wider anteriorly and tapering posteriorly. Prostomium broadly rounded (Fig. 7A), without eyes. Antennae and palps short, cirriform; antennae inserted mid-dorsally on the prostomium; palps inserted laterally. Peristomium achaetous, with two rings of length similar to the following segments. Jaw apparatus brown, well visible through the specimen body. Mandibles rod-like, with straight, serrated cutting edge (with around 8 teeth in smaller specimens, Fig. 7B) and weakly sclerotized apophyses, shorter than cutting edges. In larger specimens, the cutting edge teeth are usually worn and the apohyses are enlarged longitudinally (Fig. 7E). Maxillae of P-type (also after moulting) with asymmetric forceps; left forceps narrow and finely toothed (up to 35? teeth), right forceps wider and coarsely toothed (~15 teeth) (Fig. 7F); seven free denticles (D1–7; Fig. 7C, F), D1 comb-like coarsely toothed, similar to right forceps, D2 shovellike with an outer larger tooth and coarse teeth, D4–6 shovel-like with smaller teeth slightly increasing in number anteriorly, D7 shovel-like, much broader than the others; carrier-like structure with a toothed ridge on each side at the base of the bifurcation (Fig. 7F) and a posteriorly fimbriate handle (Fig. 7C). Parapodia uniramous, with conical acicular lobes, inconspicuous pre-chaetal lamellae, long sub-acicular lobes and conical dorsal cirri inserted sub-distally on the parapodia (Fig. 7D); ventral cirri absent. Subacicular lobes with a short needle-like protruding acicula (Fig. 7H). Chaetae relatively short and stiff; supra-acicular chaetae simple, tapering distally, smooth or very finely serrated, up to 7 per fascicle (Fig. 7I); sub-acicular chaetae compound with sub-distally serrated shafts and falcate, lightly serrated blades (Fig. 7G), up to 7 per fascicle. Pygidium with terminal anus, a pair of short cirriform anal cirri (spherical and almost inconspicuous in smaller specimens) and a median papilla. Remarks According to the phylogenetic analysis (Fig. 2), O. geoffreadi sp. nov. is close to the species O. langstrumpae Wiklund et al ., 2012, O. sadina Ravara, Marçal, Wiklund & Hilário, 2015, O. cantabrica Nuñez, Riera & Maggio, 2014, O. scutellus Wiklund, Glover & Dahlgren, 2009, O. lusa Ravara, Marçal, Wiklund & Hilário, 2015, O. batillus Wiklund et al ., 2012 and O. chemecoli sp. nov. (Wiklund et al . 2009, 2012; Nuñez et al . 2014; Ravara et al . 2015). However, unlike O . geoffreadi sp. nov., all those species have well-developed parapodial lobes and cirri, and only two of them ( O. langstrumpae and O. cantabrica ) have mandibulae with a straight cutting edge but without membranous apophyses. Three other species that are not included in the phylogenetic analysis have mandibulae with a straight, serrated cutting edge: O. pachysoma Hilbig & Blake, 1991 from the W Atlantic (604–2065 m depth), O. natans Pfannenstiel, 1975 from the Red Sea (intertidal) and O. kagoshimaensis Miura, 1997 from the W Pacific (197 m depth) (Pfannenstiel 1975; Hilbig & Blake 1991; Miura 1997). Nevertheless, the presence of a membranous apophyse below the cutting edge is not clear for the two latter species, and the cutting edge of the mandibulae of O. pachysoma is much wider and also serrated on its internal border. Furthermore, the maxillary, parapodial and chaetal morphology of all these species is different from that of O. geoffreadi sp. nov. Ecology and distribution NE Atlantic: Gulf of Cadiz (Moroccan Margin). Found in experimentally deployed wood and alfalfa substrata, at 698–1100 m depth (this study). : Published as part of Ravara, Ascensão, Wiklund, Helena & Cunha, Marina R., 2021, Four new species and further records of Dorvilleidae (Annelida, Polychaeta) from deep-sea organic substrata, NE Atlantic, pp. 44-81 in European Journal of Taxonomy 736 on pages 56-59, DOI: 10.5852/ejt.2021.736.1251, http://zenodo.org/record/4570204 : {"references": ["Wiklund H., Altamira I. V., Glover A. G., Smith C. R., Baco A. R. & Dahlgren T. G. 2012. Systematics and biodiversity of Ophryotrocha (Annelida, Dorvilleidae) with descriptions of six new species from deep-sea whale-fall and wood-fall habitats in the north-east Pacific. Systematics and Biodiversity 10 (2): 243 - 259. https: // doi. org / 10.1080 / 14772000.2012.693970", "Ravara A., Marcal A. R., Wiklund H. & Hilario A. 2015. First account on the diversity of Ophryotrocha (Annelida, Dorvilleidae) from a mammal-fall in the deep-Atlantic Ocean with the description of three new species. Systematics and Biodiversity 13 (6): 555 - 570. https: // doi. org / 10.1080 / 14772000.2015.1047428", "Nunez J., Riera R. & Maggio Y. 2014. A new Ophryotrocha species (Polychaeta: Dorvilleidae) from circalittoral seabeds of the Cantabrian Sea (north-east Atlantic Ocean). Journal of the Marine Biological Association of the United Kingdom 94 (1): 115 - 119. https: // doi. org / 10.1017 / s 0025315413001082", "Wiklund H., Glover A. G. & Dahlgren T. G. 2009. Three new species of Ophryotrocha (Annelida: Dorvilleidae) from a whale-fall in the North-East Atlantic. Zootaxa 2228 (1): 43 - 56. http: // doi. org / 10.11646 / zootaxa. 2228.1.3", "Hilbig B. & Blake J. A. 1991. Dorvilleidae (Annelida: Polychaeta) from the U. S. Atlantic slope and rise. Description of two new genera and 14 new species, with generic revision of Ophryotrocha. Zoologica Scripta 20 (2): 147 - 183. https: // doi. org / 10.1111 / j. 1463 - 6409.1991. tb 00281. x", "Pfannenstiel H. D. 1975. Ophryotrocha natans n. sp. (Polychaeta, Dorvilleidae): ein simultanzwitter mit acht mannlichen segmenten aus dem Golf von Aqaba. Zoologischer Anzeiger 195 (1 - 2): 1 - 7.", "Miura T. 1997. Two new species of the genus Ophryotrocha (Polychaeta, Iphitimidae) from Kagoshima Bay. Bulletin of Marine Science 60 (2): 300 - 305."]}