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A new species and four new records of sedentary polychaetes from the Canadian High Arctic

Published online by Cambridge University Press:  21 July 2016

Eduardo López ,
Fredéric Olivier ,
Cindy Grant  and
Philippe Archambault
Eduardo López*
Affiliation:
Departamento de Biología, Universidad Autónoma de Madrid, Darwin 2, 28049 Madrid, Spain
Fredéric Olivier
Affiliation:
Departement Milieux et Peuplements Aquatiques, Muséum National d'Histoire Naturelle, UMR 7208 BOREA MNHN/CNRS/P6/IRD, Station Marine de Concarneau, Place de la croix, 29182 Concarneau, France
Cindy Grant
Affiliation:
Institut des Sciences de la Mer, Université du Québec à Rimouski, 310 allée des Ursulines, Rimouski, QC G5L 3A1, Canada
Philippe Archambault
Affiliation:
Institut des Sciences de la Mer, Université du Québec à Rimouski, 310 allée des Ursulines, Rimouski, QC G5L 3A1, Canada
*
Correspondence should be addressed to: E. López, Departamento de Biología, Universidad Autónoma de Madrid, Darwin 2, 28049 Madrid, Spain email: [email protected]
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Abstract

During ArcticNet surveys aboard ‘CCGS Amundsen’ in 2011, several subtidal stations located in Canadian Archipelago were sampled in order to study the composition of their benthic communities. Among the abundant material sampled, several specimens of rare polychaete species were found. Examination of this material showed four species not previously recorded in the area, and a new species described herein. Descriptions of these specimens are given in this work. Ophelina brattegardi Kongsrud et al., 2011 is characterized by a body composed of 27–28 chaetigers, by having the parapodia of the last four chaetigers shifted to the ventral side of the body, and by lacking branchiae in mid-body chaetigers. Macrochaeta polyonix Eliason, 1962 is unique within the genus in having several (instead of one or two) compound neurochaetae in anterior parapodia. Chaetozone acuta Banse & Hobson, 1968 is characterized by having spines from anterior third of the body and arranged in bundles composed of just a few chaetae. Chaetozone jubata Chambers & Woodham, 2003 can be distinguished from similar species by having very long capillary chaetae from chaetiger 2 or 3. Finally, Dialychone hervyae n. sp. is characterized by bearing four pairs of radioles with narrow flanges, by the bilobed tip of its first peristomial ring that projects beyond the collar, and by the paleate thoracic notochaetae bearing long mucros.

Keywords

OphelinaMacrochaetaChaetozoneDialychoneSabellidae
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 97 , Issue 8 , December 2017 , pp. 1685 - 1694
Copyright
Copyright © Marine Biological Association of the United Kingdom 2016 

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References

REFERENCES

Ambrose, W.G. Jr., Renaud, P.E., Cochrane, K.J., Denisenko, S.J. and Skardhamar, J. (2009) Polychaete diversity patterns on two Arctic shelves: impacts of ice and primary production? Zoosymposia 2, 457–485.CrossRefGoogle Scholar
Archambault, P., Snelgrove, P.V.R., Fisher, J.A.D., Gagnon, J.-M., Garbary, D.J., Harvey, M., Kenchington, E.L., Lesage, V., Levesque, M., Lovejoy, C., Mackas, D.L., McKindsey, C.W., Nelson, J.R., Pepin, P., Piché, L. and Poulin, M. (2010) From sea to sea: Canada's three oceans of biodiversity. PLoS ONE 5, e12182. doi: 10.1371/journal.pone.0012182.CrossRefGoogle ScholarPubMed
Bakken, T., Kongsrud, J.A., Oug, E., Cochrane, S.K.J., Moen, T.L. and Solbakken, B.E.B. (2010) Polychaetes from Jan Mayen (Annelida, Polychaeta). Polar Research 29, 1–21.CrossRefGoogle Scholar
Banse, K. (1969) Acrocirridae n. fam. (Polychaeta Sedentaria). Journal of the Fisheries Research Board, Canada 26, 2595–2620.CrossRefGoogle Scholar
Banse, K. and Hobson, K.D. (1968) Benthic polychaetes from Puget Sound, Washington, with remarks on four other species. Proceedings of the United States National Museum 125(3667), 1–53.CrossRefGoogle Scholar
Blake, J.A. (1996) Chapter 8. Family Cirratulidae Ryckholdt, 1851. In Blake, J.A., Hilbig, B. and Scott, P.H. (eds) Taxonomic Atlas of the Santa Maria Basin and Western Santa Barbara Channel, Volume 6. Annelida Part 3. Polychaeta: Orbiniidae to Cossuridae. Santa Barbara, CA: Santa Barbara Museum of Natural History, pp. 263–384.Google Scholar
Blake, J.A. (2006) New species and records of deep-water Cirratulidae (Polychaeta) from off Northern California. Scientia Marina 70 (Suppl.), 45–57.CrossRefGoogle Scholar
Blake, J.A. (2015) New species of Chaetozone and Tharyx (Polychaeta: Cirratulidae) from the Alaskan and Canadian Arctic and the Northeastern Pacific, including a description of the lectotype of Chaetozone setosa Malmgren from Spitsbergen in the Norwegian Arctic. Zootaxa 3919, 501–552.CrossRefGoogle ScholarPubMed
Carr, C.M. (2012) Polychaete diversity and distribution patterns in Canadian marine waters. Marine Biodiversity 42, 93–107.CrossRefGoogle Scholar
Chambers, S.J. (2000) A redescription of Chaetozone setosa Malmgren, 1867 including a definition of the genus and a description of a new species of Chaetozone (Polychaeta: Cirratulidae) from the northeast Atlantic. Bulletin of Marine Science 67, 587–596.Google Scholar
Chambers, S.J. and Woodham, A. (2003) A new species of Chaetozone (Polychaeta: Cirratulidae) from deep waters in the northeast Atlantic, with comments on the diversity of the genus in cold northern waters. Hydrobiologia 496, 41–48.CrossRefGoogle Scholar
Darnis, G., Robert, D., Pomerleau, C., Link, H., Archambault, P., Nelson, R.J., Geoffroy, M., Tremblay, J-.E., Lovejoy, C., Ferguson, S.H., Hunt, B.P.V. and Fortier, L. (2012) Current trends in Canadian Arctic marine ecosystems; II. Heterotrophic web, pelagic-benthic coupling, and biodiversity. Climatic Change 115, 179–205.CrossRefGoogle Scholar
Eliason, A. (1962) Die Polychaeten der Skagerrak-Expedition 1933. Zoologiska Bidrag Från Uppsala 33, 207–293.Google Scholar
Forest, A., Tremblay, J-.E., Gratton, Y., Martin, J., Gagnon, J., Darnis, G., Sampei, M., Fortier, L., Ardyna, M., Gosselin, M., Hattori, H., Nguyen, D., Maranger, R., Vaqué, D., Marrrasé, C., Pedrós-Alió, C., Sallon, A., Michel, C., Kellogg, C., Deming, J., Shadwick, E., Thomas, H., Link, H., Archambault, P. and Piepenburg, D. (2011) Biogenic carbon flows through the planktonic food web of the Amundsen Gulf (Arctic Ocean): a synthesis of field measurements and inverse modelling analyses. Progress in Oceanography 91, 410–436.CrossRefGoogle Scholar
Gavrilchuk, K. and Lesage, V. (2014) Large-scale marine development projects (mineral, oil and gas, infrastructure) proposed for Canada's North. Canadian Technical Report of Fisheries and Aquatic Sciences 3069, 1–84.Google Scholar
Giangrande, A. (1992) The genus Chone (Polychaeta, Sabellidae) in the Mediterranean Sea with description of C. longiseta n. sp. Bolletino Zoologico 59, 517–529.CrossRefGoogle Scholar
Goldsmit, J., Howland, K.L. and Archambault, P. (2014) Establishing a baseline for early detection of non-indigenous species in ports of the Canadian Arctic. Aquatic Invasions 9, 327–342.CrossRefGoogle Scholar
Hardy, S.M., Carr, C.M., Hardman, M., Steinke, D., Corstophine, E. and Mah, C. (2011) Biodiversity and phylogeography of Arctic marine fauna: insights from molecular tools. Marine Biodiversity 41, 195–210.CrossRefGoogle Scholar
Hartley, J.P. (1981) Five species of Polychaete new to the British waters. Journal of the Marine Biological Society of the United Kingdom 61, 279–280.Google Scholar
Hartman, O. (1965) Deep-water benthic polychaetous annelids off New England to Bermuda and other North Atlantic areas. Allan Hancock Foundation Publications, Occasional Paper 28, 1–378.Google Scholar
Kongsrud, J.A., Bakken, T. and Oug, E. (2011) Deep-water species of the genus Ophelina (Annelida, Opheliidae) in the Nordic Seas, with the description of Ophelina brattegardi sp. nov. Italian Journal of Zoology 78(S1), 95–111.CrossRefGoogle Scholar
Leu, E., Søreide, J.E., Hessen, D.O., Falk-Petersen, S. and Berge, J. (2011) Consequences of changing sea ice cover for primary and secondary producers in the European Arctic shelf seas: timing, quantity, and quality. Progress in Oceanography 90, 18–32.CrossRefGoogle Scholar
Link, H., Chaillou, G., Forest, A., Piepenburg, D. and Archambault, P. (2013) Multivariate benthic ecosystem functioning in the Arctic – benthic fluxes explained by environmental parameters in the southeastern Beaufort Sea. Biogeosciences 10, 5911–5929.CrossRefGoogle Scholar
MacDonald, I.R., Bluhm, B.A., Iken, K., Gagaev, S. and Strong, S. (2010) Benthic macrofauna and megafauna assemblages in the Arctic deep-sea Canada Basin. Deep-Sea Research II 57, 136–152.CrossRefGoogle Scholar
Olivier, F., San Martín, G. and Archambault, P. (2013) A new species of Streptospinigera Kudenov, 1983 (Polychaeta, Syllidae, Anoplosyllinae) from the Arctic and north-western Atlantic with a key to all species of the genus. Polar Biology 36, 1499–1507.CrossRefGoogle Scholar
Parapar, J. and Moreira, J. (2009) Polychaeta of the “DIVA-Artabria I” project (cruise 2002) in the continental shelf and upper slope off Galicia (NW Spain). Cahiers de Biologie Marine 50, 57–78.Google Scholar
Parapar, J., Moreira, J. and Helgason, G.V. (2011) Distribution and diversity of the Opheliidae (Annelida, Polychaeta) on the continental shelf and slope of Iceland, with a review of the genus Ophelina in northeast Atlantic waters and description of two new species. Organisms Diversity and Evolution 11, 83–105.CrossRefGoogle Scholar
Quijón, P.A. and Snelgrove, P.V. (2005) Polychaete assemblages of a sub-arctic Newfoundland fjord: habitat, distribution, and identification. Polar Biology 28, 495–505.CrossRefGoogle Scholar
Rouse, G.W. and Pleijel, F. (2001) Polychaetes. Oxford: Oxford University Press.Google Scholar
Selim, S.A., Rzhavsky, A.V. and Britayev, T.A. (2012) Dialychone and Paradialychone (Polychaeta: Sabellidae) from the Mediterranean coast of Egypt with description of Dialychone egyptica sp. n. Invertebrate Zoology 9, 105–114.CrossRefGoogle Scholar
Siddall, M.E., Borda, E. and Rouse, G.W. (2004) Toward a tree of life for Annelida. In Cracraft, J. and Donoghue, M.J. (eds) Assembling the tree of life. Oxford: Oxford University Press, pp. 237–251.CrossRefGoogle Scholar
Smetacek, V. and Nicol, S. (2005) Polar ocean ecosystems in a changing world. Nature 437, 362–368.CrossRefGoogle Scholar
Tovar-Hernández, M.A. (2007a) On some species of Chone Krøyer, 1856 (Polychaeta: Sabellidae) from world-wide localities. Zootaxa 1518, 31–68.CrossRefGoogle Scholar
Tovar-Hernández, M.A. (2007b) Revision of Chone Krøyer, 1856 (Polychaeta: Sabellidae) from North America and descriptions of four new species. Journal of Natural History 41, 511–566.CrossRefGoogle Scholar
Tovar-Hernández, M.A. (2008) Phylogeny of Chone Krøyer, 1856 (Polychaeta: Sabellidae) and related genera. Journal of Natural History 42, 2193–2226.CrossRefGoogle Scholar
Tovar-Hernández, M.A., Licciano, M. and Giangrande, A. (2007) Revision of Chone Krøyer, 1856 (Polychaeta: Sabellidae) from the Eastern Central Atlantic and Mediterranean Sea with descriptions of two new species. Scientia Marina 71, 315–338.CrossRefGoogle Scholar
Vermeij, G.J. and Roopnarine, P.D. (2008) The coming Arctic invasion. Science 321, 780–781.CrossRefGoogle ScholarPubMed
Wassmann, P., Duarte, C.M., Agust, S. and Sejr, M.K. (2011) Footprints of climate change in the Arctic marine ecosystem. Global Change Biology 17, 1235–1249.CrossRefGoogle Scholar