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The community associated with biogenic reefs formed by the polychaete, Serpula vermicularis

Published online by Cambridge University Press:  22 July 2011

Nicola D. Chapman
Affiliation:
School of Life Sciences, Heriot-Watt University, Riccarton, Edinburgh EH14 4AS, UK
Colin G. Moore*
Affiliation:
School of Life Sciences, Heriot-Watt University, Riccarton, Edinburgh EH14 4AS, UK
Dan B. Harries
Affiliation:
School of Life Sciences, Heriot-Watt University, Riccarton, Edinburgh EH14 4AS, UK
Alastair. R. Lyndon
Affiliation:
School of Life Sciences, Heriot-Watt University, Riccarton, Edinburgh EH14 4AS, UK
*
Correspondence should be addressed to: Colin G. Moore, School of Life Sciences, Heriot-Watt University, Riccarton, Edinburgh, EH14 4AS, UK email: [email protected]

Abstract

The study aims to provide the first detailed account of the diversity and composition of the community associated with biogenic reefs formed by serpulid worms. Ten reefs (aggregations of calcareous Serpula vermicularis tubes), spanning a broad size-range, were collected from Loch Creran, Scotland, a Special Area of Conservation designated principally for the protection of its biogenic reefs. Total faunal abundance was strongly linearly related to reef weight, whilst taxon richness exhibited a hyperbolic relationship with reef size. 278 taxa were recorded from the ten reefs, with a reef of 0.1 m2 area supporting 163 taxa and 12756 individuals, which appears to represent considerable augmentation of diversity and abundance for sedimentary areas of the loch where the reefs occur. The reef assemblage was dominated by polychaetes (94 taxa), molluscs (70 taxa) and crustaceans (45 taxa). Species composition varied with reef size, although reefs greater than 25 cm width exhibited relatively little variation. In comparison with other biogenic polychaete habitats, S. vermicularis reefs appear to support a highly diverse community, which exhibits a high degree of similarity with that found in association with aggregations of the horse mussel, Modiolus modiolus. The presence of the Connemara clingfish, Lepadogaster candollei, rarely recorded at such a northerly latitude, on several reefs, indicates that the reef habitat may provide a stronghold for this species at the edge of its biogeographical range.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2011

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References

REFERENCES

Black, K.D., Hughes, D.J., Provost, P.G. and Pereira, P.M.F. (2000) Broad scale survey and mapping of seabed biota in Loch Creran, Argyll. Scottish Natural Heritage Commissioned Report No. F98AA408, 73 pp.Google Scholar
Bosence, D.W.J. (1973) Recent serpulid reefs, Connemara, Eire. Nature 242, 4041.Google Scholar
Bosence, D.W.J. (1979) The factors leading to aggregation and reef formation in Serpula vermicularis L. In Larwood, G. and Rosen, B.R. (eds) Biology and systematics of colonial organisms. London: Academic Press, pp. 299318.Google Scholar
Connor, D.W., Dalkin, M.J., Hill, T.O., Holt, R.H.F. and Sanderson, W.G. (1997) Marine biotope classification for Britain and Ireland. Volume 2. Sublittoral biotopes Version 97.06. Peterborough: Joint Nature Conservation Committee, 448 pp.Google Scholar
Dias, A.S. 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.Google Scholar
Dodd, J., Baxter, L. and Hughes, D.J. (2009) Mapping Serpula vermicularis (Polycheata: Serpulidae) aggregations in Loch Teacuis, western Scotland, a new record. Marine Biology Research 5, 200205.Google Scholar
Dubois, S., Retière, C. and Olivier, F. (2002) Biodiversity associated with Sabellaria alveolata (Polychaeta: Sabellariidae) reefs: effects of human disturbances. Journal of the Marine Biological Association of the United Kingdom 82, 817826.CrossRefGoogle Scholar
Dubois, S., Commito, J.A., Olivier, F. and Retière, C. (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.Google Scholar
Gage, J. (1972) A preliminary survey of the benthic macrofauna and sediments in Lochs Etive and Creran, sea-lochs along the west coast of Scotland. Journal of the Marine Biological Association of the United Kingdom 52, 237276.Google Scholar
George, C.L. and Warwick, R.M. (1985) Annual macrofauna production in a hard-bottom reef community. Journal of the Marine Biological Association of the United Kingdom 65, 713735.Google Scholar
Haines, J.L. and Maurer, D. (1980a) Quantitative faunal associates of the serpulid polychaete Hydroides diathus. Marine Biology 56, 4347.Google Scholar
Haines, J.L. and Maurer, D. (1980b) Benthic invertebrates associated with a serpulid polychaete assemblage in a temperate estuary. Internationale Revue der gesamten Hydrobiologie 65, 643656.Google Scholar
Hayward, P.J., Ryland, J.S. (1990) The marine fauna of the British Isles and north-west Europe. Oxford: Clarendon Press, 996 pp.Google Scholar
Howson, C.M. and Picton, B.E. (1997) The species directory of the marine fauna and flora of the British Isles and surrounding seas. Belfast: The Ulster Museum, 508 pp.Google Scholar
Kaiser, M.J., Cheney, K., Spence, F.E., Edwards, D.B. and Radford, K. (1999) Fishing effects in northeast Atlantic shelf seas: patterns in fishing effort, diversity and community structure VII. The effects of trawling disturbance on the fauna associated with the tubeheads of serpulid worms. Fisheries Research 40, 195205.Google Scholar
Kirkwood, J.M. and Burton, H.R. (1988) Macrobenthic species assemblages in Ellis Fjord, Vestfold Hills, Antarctica. Marine Biology 97, 445457.Google Scholar
Mair, J.M., Moore, C.G., Kingston, P.F. and Harries, D.B. (2000) A review of the status, ecology and conservation of horse mussel Modiolus modiolus beds in Scotland. Scottish Natural Heritage Commissioned Report No. F99PA08, 89 pp.Google Scholar
Minchin, D. (1987) Serpula vermicularis L. (Polychaeta: Serpulidae) reef communities from the west coast of Ireland. Irish Naturalists' Journal 22, 314316.Google Scholar
Moore, C.G., Saunders, G.R. and Harries, D.B. (1998) The status and distributional ecology of reefs of Serpula vermicularis L. (Polychaeta: Serpulidae) in Scotland. Aquatic Conservation: Marine and Freshwater Ecosystems 8, 645656.Google Scholar
Moore, C.G., Harries, D.B., Lyndon, A.R., Saunders, G.R. and Conway, T.R. (2003) Quantification of serpulid biogenic reef coverage of the sea bed (Polychaeta: Serpulidae) using a video transect technique. Aquatic Conservation: Marine and Freshwater Ecosystems 13, 137146.Google Scholar
Moore, C.G., Saunders, G.R., Harries, D.B., Mair, J.M., Bates, C.R., Lyndon, A.R. (2006) The establishment of site condition monitoring of the subtidal reefs of Loch Creran Special Area of Conservation. Scottish Natural Heritage Commissioned Report No. 151, 119 pp.Google Scholar
Moore, C.G., Bates, C.R., Mair, J.M., Saunders, G.R., Harries, D.B. and Lyndon, A.R. (2009) Mapping serpulid worm reefs (Polychaeta: Serpulidae) for conservation management. Aquatic Conservation: Marine and Freshwater Ecosystems, 19, 226236.Google Scholar
Moore, P.G. (1973) The kelp fauna of northeast Britain. II. Multivariate classification: turbidity as an ecological factor. Journal of Experimental Marine Biology and Ecology 13, 127163.Google Scholar
NBN, Gateway (2011) Grid map of records on the Gateway for Connemara Clingfish (Lepadogaster candollei) <http://data.nbn.org.uk/gridMap/gridMap.jsp?allDs=1&srchSpKey=NBNSYS0000176048> (accessed 1 February 2011).+(accessed+1+February+2011).>Google Scholar
Pickard, J., Adamson, D.A. and Heath, C.W. (1986) The evolution of Watts Lake, Vestfold Hills, East Antarctica, from marine inlet to freshwater lake. Palaeogeography, Palaeoclimatology, Palaeoecology 53, 271288.Google Scholar
Poloczanska, E.S., Hughes, D.J. and Burrows, M.T. (2005) Underwater television observations of Serpula vermicularis (L.) reefs and associated mobile fauna in Loch Creran, Scotland. Estuarine, Coastal and Shelf Science 61, 425435.Google Scholar
Ramosa, A. and San Martin, G. (1999) On the finding of a mass occurrence of Serpula narconensis Baird, 1885 (Polychaeta, Serpulidae) in South Georgia (Antarctica). Polar Biology 22, 379383.Google Scholar
Schwindt, E., Bortolos, A. and Iribarne, O.O. (2001) Invasion of a reef-builder polychaete: direct and indirect impacts on the native benthic community structure. Biological Invasions 3, 137149.Google Scholar
Schwindt, E. and Iribarne, O.O. (2000) Settlement sites, survival and effects on benthos of an introduced reef-building polychaete in a SW Atlantic coastal lagoon. Bulletin of Marine Science 67, 7382.Google Scholar
Smith, A.M., McGourty, C.R., Kregting, L. and Elliot, A. (2005) Subtidal Galeolaria hystrix (Polychaeta: Serpulidae) reefs in Paterson Inlet, Stewart Island, New Zealand. New Zealand Journal of Marine and Freshwater Research 39, 12971304.Google Scholar
Ten Hove, H.A. and Van den Hurk, P. (1993) A review of recent and fossil serpulid ‘reefs’; actuopalaeontology and the ‘Upper Malm’ serpulid limestones in NW Germany. Geologie en Mijnbouw 72, 2367.Google Scholar
Wheeler, A. (1978) Key to the fishes of northern europe. London: Frederick Warne, 380 pp.Google Scholar