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Reproduction of the biogenic reef-forming honeycomb worm Sabellaria alveolata in Ireland

Published online by Cambridge University Press:  14 January 2010

S.C. Culloty*
Affiliation:
Department of Zoology, Ecology and Plant Science and Aquaculture and Fisheries Development Centre, University College Cork, Enterprise Centre, Distillery Fields, North Mall, Cork, Ireland
E. Favier
Affiliation:
Department of Zoology, Ecology and Plant Science and Aquaculture and Fisheries Development Centre, University College Cork, Enterprise Centre, Distillery Fields, North Mall, Cork, Ireland
M. Ní Riada
Affiliation:
Department of Zoology, Ecology and Plant Science and Aquaculture and Fisheries Development Centre, University College Cork, Enterprise Centre, Distillery Fields, North Mall, Cork, Ireland
N.F. Ramsay
Affiliation:
Department of Zoology, Ecology and Plant Science and Aquaculture and Fisheries Development Centre, University College Cork, Enterprise Centre, Distillery Fields, North Mall, Cork, Ireland
R.M. O'Riordan
Affiliation:
Department of Zoology, Ecology and Plant Science and Aquaculture and Fisheries Development Centre, University College Cork, Enterprise Centre, Distillery Fields, North Mall, Cork, Ireland
*
Correspondence should be addressed to: S.C. Culloty, Department of Zoology, Ecology and Plant Science, University College Cork, Enterprise Centre, Distillery Fields, North Mall, Cork, Ireland email: [email protected]

Abstract

The stage of development of the gametes of both male and female honeycomb worms Sabellaria alveolata (L.) was examined, using histology, over a 14-month period. Samples came from Howes Strand and Garrettstown, County Cork in south-west Ireland. A clear cycle of both male and female gametogenesis was evident, with a distinct peak in the summer (June–September) when the majority of them were ripe. During October–January a small proportion of males contained abundant spermatozoa, but no mature oocytes were found. Over the whole sampling period the ratio of males:females was 1.4:1. Further south in Roches de la Fosse in France at the centre of its range, two spawnings and an even sex-ratio have been reported.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2010

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References

REFERENCES

Almaça, C. (1987). Crabs of the Sabellaria alveolata (Linnaeus, 1767) community. Egg number and population size in Pilumnus hirtellus (Linnaeus, 1761) and Porcellana platycheles (Pennant, 1777). Arquivos do Museu Bocage Nova Serie 1, 1932.Google Scholar
Anadón, N. (1981). Contribución al conocimiento de la fauna bentónica de la Ría de Vigo. III. Estudio de los arrecifes de Sabellaria alveolata (L.) (Polychaeta, Sedentaria). Investigacion Pesquera Barcelona 45, 105122.Google Scholar
Bhaud, M. and Gruet, Y. (1984). Variation saisonnière du nombre et de la taille des ovocytes chez Sabellaria alveolata (Linné) (Polychaeta; Sabellariidae) et effets des paramètres climatiques. In Hutchings, PA (ed.) Proceedings of the First International Polychaete Conference. Sydney. The Linnean Society of New South Wales, pp. 450460.Google Scholar
Cazaux, C. (1964) Développement larvaire de Sabellaria alveolata (Linné). Bulletin de l'Institut Océanographie de Monaco 62, 115.Google Scholar
Commito, J.A., Celano, E.A., Celico, H.J., Como, S. and Johnson, C.P. (2005) Mussels matter: postlarval dispersal dynamics altered by a spatially complex ecosystem engineer. Journal of Experimental Marine Biology and Ecology 316, 133147.CrossRefGoogle Scholar
Cotter, E., O'Riordan, R.M. and Myers, A.A. (2003) A histological study of reproduction in the serpulids Pomatoceros triqueter and Pomatoceros lamarckii (Annelida: Polychaeta). Marine Biology 142, 905914.CrossRefGoogle Scholar
De Grave, S. and Whitaker, A. (1997) The occurrence of a subtidal Sabellaria alveolata (L.) reef off Wicklow Head, Irish Sea. Irish Naturalists’ Journal 25, 416418.Google Scholar
Dehorne, A. (1911) Recherches sur la division de la cellule. II. Homéotypie et hétérotypie chez les annélides, polychètes et les trématodes. Archives de Zoologie Experimental et Générale 9, 1175.Google Scholar
Dixon, D.R. (1981) Reproductive biology of the serpulid Ficopomatus (Mercierella) enigmaticus in the Thames Estuary, S.E. England. Journal of the Marine Biological Association of the United Kingdom 61, 805815.CrossRefGoogle Scholar
Dubois, S., Commito, J.A., Olivier, F. and Retière, (2006) Effects of epibionts on Sabellaria alveolata (L.) biogenic reefs and their associated fauna in the Bay of Mont Saint-Michel. Estuarine, Coastal and Shelf Science 68, 635646.CrossRefGoogle Scholar
Fauré-Fremiet, E. (1921) La maturation et l'activation expérimentale de l'oeuf chez les Sabellaria. Comptes Rendus de Société de Biologie 85, 810811.Google Scholar
Fauré-Frémiet, E. (1924) L'oeuf de Sabellaria alveolata L. Archives d'Anatomé Microscopique 20, 211342.Google Scholar
Giangrande, A. (1997) Polychaete reproductive patterns, life cycles and life histories: an overview. Oceanography and Marine Biology: an Annual Review 35, 323386.Google Scholar
Gruet, Y. (1986) Spatio-temporal changes of Sabellarian reefs built by the sedentary polychaete Sabellaria alveolata (Linné). PSZNI: Marine Ecology 7, 303319.Google Scholar
Gruet, Y. (1988) Biologie et ecologie de l'annélide polychète Sabellaria alveolata (Linné). In Caline, B., Legendre, C., Le Rhun, J., L'Homer, A., Mathieu, R. and Zisinden, R. (eds) Le récifs a annélides (hermelles) en baie du Mont Saint-Michel. Orléans: BRGM Editions, pp. 2342.Google Scholar
Gruet, Y. and Lassus, P. (1983) Contribution à l’étude de la biologie reproductive d'une population naturelle de l'annélide polychète Sabellaria alveolata (Linné). Annales de l'Institut Océanographique Paris 59, 127140.Google Scholar
Hiscock, K., Southward, A., Tittley, I. and Hawkins, S. (2004) Effects of changing temperature on benthic marine life in Britain and Ireland. Aquatic Conservation: Marine and Freshwater Ecosystems 14, 333362.CrossRefGoogle Scholar
Holt, T.J., Rees, E.I., Hawkins, S.J. and Seed, R. (1998) Biogenic reefs (volume IX). An overview of dynamic and sensitivity characteristics for conservation management of marine SACs. Scottish Association for Marine Science (UK MArine SACs Project), 170 pp.Google Scholar
Kirtley, D.W. (1968) The reef builders. Natural History New York 4045.Google Scholar
Kirtley, D.W. (1992) Worm reefs built to last. Florida Ocean Magazine 13, 1219.Google Scholar
Mettam, C., Conneely, M.E. and White, S.J. (1994) Benthic macrofauna and sediments in the Severn Estuary. Biological Journal of the Linnean Society 51, 7181.CrossRefGoogle Scholar
Molinier, R. and Picard, J. (1953) Notes biologiques à propos d'un voyage d’étude sur les côtes de Sicile. Annales de l'Institut Océanographique Paris 28, 164187.Google Scholar
Porras, R., Bataller, J.V. and Murgui, E. (1996) Reef building worms in Iberian Mediterranean Coasts. In Özhan, E (ed.) Proceedings of the Second International Conference on the Mediterranean Coastal Environment (MEDCOAST 95), Tarragona, Spain 24–27 October 1995, pp. 8794.Google Scholar
Ryland, J.S. and Nelson-Smith, A. (1974) Littoral and benthic investigations on the west coast of Ireland—IV. (Section A: Faunistic and ecological studies.) Some shores in Counties Clare and Galway. Proceedings of the Royal Irish Academy 75B, 245266.Google Scholar
Simkanin, C., Power, A.M., Myers, A., McGrath, D., Southward, A., Mieszkowska, N., Leaper, R. and O'Riordan, R. (2005) Using historical data to detect temporal changes in the abundances of intertidal species on Irish shores. Journal of the Marine Biological Association of the United Kingdom 85, 13291340.CrossRefGoogle Scholar
Sousa Dias, A. and Paula, J. (2001) Associated fauna of Sabellaria alveolata colonies on the central coast of Portugal. Journal of the Marine Biological Association of the United Kingdom 81, 169170.CrossRefGoogle Scholar
Sveshnikov, V.A. (1985) The life-history of the polychaetes (Polychaeta). Issledovaniya Fauny Morei 3, 112117. [In Russian.]Google Scholar
Vorberg, R. (1995) On the decrease of sabellarian reefs along the German North Sea coast. Publications du Service Géologique du Luxembourg 24, 8793.Google Scholar
Williams, G. (1954) Fauna of Strangford Lough and neighbouring coasts. Proceedings of the Royal Irish Academy 56B, 29133.Google Scholar
Wilson, D.P. (1929) The larvae of the British sabellarians. Journal of the Marine Biological Association of the United Kingdom 16, 221269.CrossRefGoogle Scholar
Wilson, D.P. (1968a) The settlement behaviour of the larvae of Sabellaria alveolata (L.). Journal of the Marine Biological Association of the United Kingdom 48, 387435.CrossRefGoogle Scholar
Wilson, D.P. (1968b) Some aspects of the development of eggs and larvae of Sabellaria alveolata (L.). Journal of the Marine Biological Association of the United Kingdom 48, 367386.CrossRefGoogle Scholar
Wilson, D.P. (1969) The honeycomb worm. Sea Front 15, 322329.Google Scholar
Wilson, D.P. (1970) The larvae of Sabellaria spinulosa and their settlement behaviour. Journal of the Marine Biological Association of the United Kingdom 50, 3352.CrossRefGoogle Scholar
Wilson, D.P. (1971) Sabellaria colonies at Duckpool, North Cornwall, 1961–1970. Journal of the Marine Biological Association of the United Kingdom 51, 509580. www1 http://www.met.ie/marine/marine_climatology.asp. Accessed 1 July 2009.CrossRefGoogle Scholar