We investigate mitochondrial (COI, 16S rDNA) and nuclear (ITS2, 28S rDNA) genetic structure of North East Atlantic lineages of Terebellides, a genus of sedentary annelids mainly inhabiting continental shelf and slope sediments. We demonstrate the presence of more than 25 species of which only seven are formally described. Species boundaries are determined with molecular data using a broad range of analytical methods. Many of the new species are common and wide spread, and the majority of the species are found in sympatry with several other species in the complex. Being one of the most regularly encountered annelid taxa in the North East Atlantic, it is more likely to find an undescribed species of Terebellides than a described one.
Descriptions are given of 18 species of copepods that live in symbiotic association with polychaete worms in European Seas. Three new genera and six new species of the family Clausiidae Giesbrecht, 1895 are described: Boreoclausia rectan. gen. et n. sp. is described from Galathowenia fragilis (Nilson & Holthe, 1985), Boreoclausia holmesi n. gen. et n. sp.is described from Myriochele danielsseni Hansen, 1879, Sheaderia bifida n. gen. et n. sp. from Euclymene oerstedii (Claparède, 1863), Vivgottoia garwoodi n. gen. et n. sp., was found inside the tail fragment of a terebellid host (probably Phisidia aurea Southward, 1956), Rhodinicola tenuis n. sp. from an unknown host, and R. similis n. sp., from Rhodine gracilor (Tauber, 1879). In addition, four other clausiid species, Clausia lubbockii Claparède, 1863, Mesnilia cluthae (T. and A.Scott, 1896), Rhodinicola gibbosus Bresciani, 1964 and R. rugosum (Giesbrecht, 1895), are redescribed in detail on the basis of newly collected material. The previously-unknown hosts of C. lubbockii were found to be species of the spionid polychaete genus Dipolydora Verrill, 1881. Clausia uniseta Bocquet & Stock, 1960 were recognized as a junior subjective synonym of C. lubbockii, and Mesnilia martinensis Canu, 1898 was recognized as a junior subjective synonym of M. cluthae. The sole species of the monotypic family Anomoclausiidae Gotto, 1964, Anomoclausia indrehusae Gotto, 1964, is redescribed based on new material. The host of A. indrehusae, reported here for the first time, is the spionid Pseudopolydora paucibranchiata (Okuda, 1937). Four new species of the family Nereicolidae Claus, 1875 are described, three belonging to the genus Anomopsyllus Sars, 1921: Anomopsyllus bifurcus n. sp. from Notomastus latericeus M. Sars, 1851, A. geminus n. sp. from Ampharete lindstroemi Malmgren, 1867, and A. hamiltonae n. sp., from Mugga wahrbergi Eliasson, 1955. The fourth new species is Vectoriella gabesensis n. sp., both sexes of which are described from the paraonid Aricidea catherinae Laubier, 1967 collected in the Mediterranean Sea off the coast of Tunisia. Another nereicolid, Sigecheres brittae Bresciani, 1964 is redescribed based on new material collected from the type host Sige fusigera Malmgren, 1865. It is recognized as a junior subjective synonym of Nereicola concinna T. Scott, 1902 and the valid name of this taxon becomes Sigecheres concinna (T. Scott, 1902) new combination. A new species of the family Spiophanicolidae Ho, 1984, Spiophanicola atlanticus n. sp., is described based on European material. Previously European material of Spiophanicola Ho, 1984 has been reported as S. spinulosus Ho, 1984, but based on consistent differences between the Californian S. spinulosus and material from Norway and the British Isles, there is sufficient justification to establish a new species for the European material. Finally one new genus and species is described which cannot be placed, with confidence, in any existing family. This new parasite, Notomasticola frondosus n. gen. et n. sp., is based on material from two hosts, a spionid (Pseudopolydora paucibranchiata) and a capitellid (Notomastus latericeus). It is highly derived and may represent a terminal branch within an existing family. The cluster of families using polychaetes as hosts is in need of revision based on a comprehensive phylogenetic analysis.
A collection of over one hundred specimens of Syllidae (Polychaeta) from the Arctic and sub-Arctic regions has been examined and identified. The specimens were obtained from 26 stations in the Barents Sea, some Norwegian fiords and localities of the northern North Sea. A total of 21 species were identified; three species (Myrianida langerhansi (Gidholm, 1967), Syllides longocirrata Örsted, 1845 and Sphaerosyllis taylori Perkins, 1981) are new reports for the Arctic Ocean; 2 species are new to science, Streptodonta exsulis sp. nov. and Trypanosyllis troll sp. nov. Streptodonta exsulis sp. nov. have 4 thick, distally strongly knobbed aciculae on each anterior parapodia, shifting to a single, slender acicula on posterior parapodia; falcigers and pseudospinigers distally bidentate; and pharyngeal tooth located centrally and relatively close to anterior rim of pharynx. Trypanosyllis troll sp. nov. have 2, occasionally 3 straight aciculae in parapodia protruding out from parapodial lobes; falcigers bidentate; and body surface densely covered by numerous, small papillae. Based on the description of these 2 new species, some modifications are proposed in the diagnoses of the genera Streptodonta San Martín & Hutchings, 2006 and Trypanosyllis Claparède, 1864.
Four species of Laonice (Annelida: Spionidae) were collected from the lower bathyal depths (3300–3700 m) in the Whittard Canyon, NE Atlantic. Two are herewith described as new species: Laonice whittardensis sp. nov. and Laonice natae sp. nov. The other two are Laonice blakei Sikorski & Jirkov, 1988 and Laonice magnacristata Maciolek, 2000. Laonice whittardensis has genital pouches appearing from chaetiger 3, prostomium free of peristomium and bidentate hooks. Laonice natae belongs to the subgenus Appelloefia nov. with prostomium distinct from the peristomium, more than two vertical rows of capillaries in several anterior chaetigers, genital pouches present on a limited number of segments or totally absent. However, the absence of pronounced anterior widening of the body together with anterior branchiae, which are remarkably (nearly twice) longer than the notopodial postchaetal lobes, the narrow lanceolate notopodial postchaetal lobes, the pronounced pointedness of all postchaetal lobes (both notopodial and neuropodial) in the anterior half of body at least, and absence of genital pouches and the size of the body all distinguish L. natae from other species belonging to this subgenus. An identification key to all nine known deep-water (>400 m depth) Laonice species in North Atlantic is given and four previously recognized sub-generic groups are formally named: Laonice, Sarsiana subgen. nov., Appelloefia subgen. nov., Norgensia subgen. nov.
Three new species of Laonice (Polychaete: Spionidae): L. galatheae, L. cricketae, L. olgae-are described from South and West Africa (along the coast from 31°14.1'S to 04°44'N) based on Danish and South African zoological collections. Arguments relative to the morphological heterogeneity of the genus Laonice are advanced. The arguments are based on the following characters: degree of fusion of prostomium with peristomium at the anterior margin, degree of variability of all numerical characters, arrangement of anterior capillaries in two or more vertical rows, presence or absence of transversal dorsal membranous crests in the "post nuchal organ" and presence of genital pouches only on very limited number of segments or other pattern. Authors think it is obvious today an existence of at least four morphologically separate groups of species inside the Laonice-genus: "L. cirrata", "L. sarsi", "L. appelloefi" and "L. norgensis" groups. Eight species names from 34 valid names in the genus are still with unclear affiliation. L. quadridentata is treated now as a junior synonym of L. brevicornis. An opinion is expressed about L. insolita not belonging to the genus Laonice because of discrepancy the generic diagnosis.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.