Hostname: page-component-cd9895bd7-p9bg8 Total loading time: 0 Render date: 2024-12-27T22:58:31.946Z Has data issue: false hasContentIssue false

Macrofaunal community responses to marina-related pollution on the south coast of England and west coast of France

Published online by Cambridge University Press:  20 February 2009

Myriam D. Callier*
Affiliation:
Institute of Marine Sciences, School of Biological Sciences, University of Portsmouth, Ferry Road, Portsmouth, P04 9LY, UK Laboratoire de Biologie et d'Écologie Marine, Université de La Rochelle, Avenue Michel Crépeau, 17042 La Rochelle, France
Robert L. Fletcher
Affiliation:
Institute of Marine Sciences, School of Biological Sciences, University of Portsmouth, Ferry Road, Portsmouth, P04 9LY, UK
Clifford H. Thorp
Affiliation:
Institute of Marine Sciences, School of Biological Sciences, University of Portsmouth, Ferry Road, Portsmouth, P04 9LY, UK
Denis Fichet
Affiliation:
Laboratoire de Biologie et d'Écologie Marine, Université de La Rochelle, Avenue Michel Crépeau, 17042 La Rochelle, France
*
Correspondence should be addressed to: Myriam D. Callier, University College Dublin, School of Biology and Environmental Science, Science Centre West Belfield, Dublin 4, Ireland email: [email protected]

Abstract

This study evaluates the influence of man-made activities on the benthic environment at two different marinas: Southsea Marina on the south coast of England, and Minimes Marina on the Atlantic coast of France. We assessed the differences in: (1) sediment percentage organic matter, particle size and heavy metal concentration, using copper (Cu), cadmium (Cd), zinc (Zn) and lead (Pb) as contamination indicators; (2) sediment elutriate toxicity (LC50) using algal (Fucus serratus) bioassay; and (3) benthic community characteristics (number of species, abundance, most contributing species (SIMPER) and biotic index (AMBI)). Canonical correspondence analysis (CCA) was performed to relate the abundance of species to the environmental variables. At both marinas, we observed an increasing gradient of contamination from outside to the innermost sites. At both marinas, the lowest macrofaunal abundance was recorded at the innermost sites and differences in benthic community structure were observed between sites. At Southsea Marina, the cirratulids Tharyx marioni and T. killariensis and the cossurid Cossura pygodactylata dominated sites outside, while the opportunistic species Capitellides girardi dominated the innermost sites. At Minimes Marina, the cirratulid Streblospio shrubsolii was abundant outside and at the middle sites but was almost absent at the innermost sites. The biotic index—AMBI—indicated that sediments in the innermost sites were heavily disturbed at Southsea Marina and slightly to moderately disturbed at Minimes Marina. In Southsea, the AMBI was positively correlated to the sediment metal concentrations (Cu, Zn and Cd) and elutriate toxicity (LC50), while in Minimes the AMBI was positively correlated to the % of sediment fine particle and elutriate toxicity (LC50).

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2009

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Alzieu, C. (2000) Impact of tributyltin on marine invertebrates. Ecotoxicology 9, 7176.CrossRefGoogle Scholar
Alzieu, C., Sanjuan, J., Borel, M. and Dreno, P. (1989) Monitoring and assessment of butyltins in Atlantic coastal waters. Marine Pollution Bulletin 20, 2226.CrossRefGoogle Scholar
Bird, P., Comber, S.D.W., Gardner, M.J. and Ravenscroft, J.E. (1996) Zinc inputs to coastal waters from sacrificial anodes. Science of the Total Environment 181, 257264.CrossRefGoogle Scholar
Biselli, S., Bester, K., Hühnerfuss, H. and Fent, K. (2000) Concentrations of the antifouling Irgarol 1051 and of organotins in water and sediments of German North and Baltic Sea marinas. Marine Pollution Bulletin 40, 233243.CrossRefGoogle Scholar
Borja, À., Franco, J. and Perez, V. (2000) A marine biotic index to establish the ecological quality of soft-bottom benthos within European estuarine and coastal environments. Marine Pollution Bulletin 40, 11001114.CrossRefGoogle Scholar
Borja, À., Muxika, I. and Franco, J. (2003) The application of a marine biotic index to different impact sources affecting soft-bottom benthic communities along European coasts. Marine Pollution Bulletin 46, 835845.CrossRefGoogle ScholarPubMed
Braithwaite, R.A. and Fletcher, R.L. (2005) The toxicity of Irgarol 1051 and Sea-Nine 211 to the non-target macroalga Fucus serratus Linnaeus, with the aid of an image capture and analysis system. Journal of Experimental Marine Biology and Ecology 322, 111121.CrossRefGoogle Scholar
Brown, C.J., Fletcher, R.L. and Eaton, R.A. (1998) Bioassays for rapid assessment of heavy metal toxicity in seawater. In The International Group on Wood Preservation. 29th Annual MeetingNetherlands, Maastricht, pp. 117.Google Scholar
Bryan, G.W. and Langston, W.J. (1992) Bioavailability, accumulation and effects of heavy metals in sediments with special reference to United Kingdom estuaries: a review. Environmental Pollution 76, 89131.CrossRefGoogle ScholarPubMed
Byers, S.C., Mills, E.L. and Stewart, P.L. (1978) A comparison of methods of determining organic carbon in marine sediments, with suggestions for a standard method. Hydrobiologia 58, 4347.CrossRefGoogle Scholar
Chapman, P.M. (1992) Pollution status of North Sea sediments—an international integrative study. Marine Ecology Progress Series 91, 313322.CrossRefGoogle Scholar
Chapman, P.M., Dexter, R.N. and Long, E.R. (1987) Synoptic measures of sediment contamination, toxicity and infaunal community composition (the Sediment Quality Triad) in San Francisco Bay. Marine Ecology 37, 7596.CrossRefGoogle Scholar
Chen, Z., Mayer, L.M., Quétel, C., Donard, O.F.X., Self, R.F.L., Jumars, P.A. and Weston, D.P. (2000) High concentrations of complex metals in the guts of deposit feeders. Limnology and Oceanography 45, 13581367.CrossRefGoogle Scholar
Clarke, K.R. and Warwick, R.M. (1994) Change in marine communities: an approach to statistical analysis and interpretation. Plymouth Marine Laboratory: Plymouth.Google Scholar
Connell, S.D. (2000) Floating pontoons create novel habitats for subtidal epibiota. Journal of Experimental Marine Biology and Ecology 247, 183194.CrossRefGoogle ScholarPubMed
Dahl, B. and Blanck, H. (1996) Toxic effects of the antifouling agent Irgarol 1051 on periphyton communities in coastal water microcosms. Marine Pollution Bulletin 32, 342350.CrossRefGoogle Scholar
Davenport, J. and Davenport, J.L. (2006) The impact of tourism and personal leisure transport on coastal environments: a review. Estuarine, Coastal and Shelf Science 67, 280292.CrossRefGoogle Scholar
Fichet, D., Boucher, G., Radenac, G. and Miramand, P. (1999a) Concentration and mobilisation of Cd, Cu, Pb and Zn by meiofauna populations living in harbour sediment: their role in the heavy metal flux from sediment to food web. Science of the Total Environment 243/244, 263272.CrossRefGoogle ScholarPubMed
Fichet, D., Radenac, G. and Miramand, P. (1999b) Experimental studies of impacts of harbour sediments resuspension to marine invertebrates: bioavailability of Cd, Cu, Pb and Zn and toxicity. Marine Pollution Bulletin 36, 509518.CrossRefGoogle Scholar
Fletcher, R.L. (1980) Studies on marine algal fouling communities in the North Atlantic. The macro-algae of floating marinas on the east and south coasts of the British Isles. Bulletin de Liaison du COIPM 8, 540.Google Scholar
Fletcher, R.L. (1991) Marine macroalgae as bioassay test organisms. In Abel, P.D. and Axiak, V. (eds) Ecotoxicology and the marine environment. London: Ellis Horwood, pp. 111131.Google Scholar
Giere, O. (1993) Meiobenthology (the microscopic fauna in aquatic sediments). Berlin: Springer-Verlag, 328 pp.Google Scholar
Giere, O., Preusse, J.H. and Dubilier, N. (1999) Tubificoides benedii (Tubificidae, Oligochaeta)—a pioneer in hypoxic and sulfidic environments. An overview of adaptative pathways. Hydrobiologia 406, 235241.CrossRefGoogle Scholar
Guerra-García, J.M. and Garcia-Gómez, J.C. (2005) Oxygen levels versus chemical pollutants: do they have similar influence on macrofaunal assemblages? A case study in a harbour with two opposing entrances. Environmental Pollution 135, 281291.CrossRefGoogle Scholar
Hall, L.W., Unger, M.A., Ziegenfuss, M.C., Sullivan, J.A. and Bushong, S.J. (1992) Butyltin and copper monitoring in a northern Chesapeake Bay marina and river system in 1989: an assessment of tributyltin legislation. Environmental Monitoring and Assessment 22, 1538.CrossRefGoogle Scholar
Haynes, D. and Loong, D. (2002) Antifoulant (butyltin and copper) concentrations in sediments from the Great Barrier Reef World Heritage Area, Australia. Environmental Pollution 120, 391396.CrossRefGoogle ScholarPubMed
La Roche, A. (2000) Detection of toxic sediment in Langstone Harbour in the South Coast of England using the novel algal bioassays procedures. BSc thesis. University of Portsmouth, 59 pp.Google Scholar
Lenihan, H.S., Oliver, J.S. and Stephenson, M.A. (1990) Changes in hard bottom communities related to boat mooring and tributyltin in San Diego Bay: a natural experiment. Marine Ecology Progress Series 60, 147159.CrossRefGoogle Scholar
McGee, B.L., Schlekat, C.E., Boward, D.M. and Wade, T.L. (1995) Sediment contamination and biological effects in a Chesapeake Bay marina. Ecotoxicology 4, 3959.CrossRefGoogle Scholar
Newell, R.C. (1962) Behavioural aspects of the ecology of Peringia (Hydrobia) ulvae (Pennant) (Gastropoda, Prosobranchia). Proceedings of the Zoological Society of London 38, 4975.CrossRefGoogle Scholar
Pearson, T.H. and Black, K.D. (2001) The environmental impacts of marine fish cage culture. In Black, K.D. (ed.) Environmental impacts of aquaculture. Sheffield: Academic Press, pp. 132.Google Scholar
Pearson, T.H. and Rosenberg, R. (1978) Macrobenthic succession in relation to organic enrichment and pollution of the marine environment. Oceanography and Marine Biology: an Annual Review 16, 229311.Google Scholar
Phillips, D.J.H. (1977) The use of biological indicator organisms to monitor trace metal pollution in marine and estuarine environments: a review. Environmental Pollution 13, 281317.Google Scholar
Pigeot, J., Miramand, P., Guyot, T., Sauriau, P.-G., Fichet, D., Le Moine, O. and Huet, V. (2006) Cadmium pathways in an exploited intertidal ecosystem with chronic cadmium inputs (Marennes-Oléron, Atlantic coast, France). Marine Ecology Progress Series 307, 101114.CrossRefGoogle Scholar
Scanlan, C.M. and Wilkinson, M. (1987) The use of seaweeds in biocide toxicity testing. Part 1. The sensitivity of different stages in the life history of Fucus and other algae to certain biocides. Marine Environmental Research 21, 1129.CrossRefGoogle Scholar
Schiff, K., Diehl, D. and Valkirs, A. (2004) Copper emissions from antifouling paint on recreational vessels. Marine Pollution Bulletin 48, 371377.CrossRefGoogle ScholarPubMed
Thomas, N.S. (1987) Aspects of the ecology of the macroinvertebrates in the intertidal soft sediments of Chichester Harbour. Portsmouth, UK: School of Biological Sciences Portsmouth Polytechnic.Google Scholar
Thomas, K.V., McHugh, M. and Waldock, M. (2002) Antifouling paint booster biocides in UK coastal waters: inputs, occurrence and environmental fate. Science of the Total Environment 293, 117127.CrossRefGoogle ScholarPubMed
Traunspurger, W. and Drews, C. (1996) Toxicity analysis of freshwater and marine sediments with meio- and macrobenthic organims: a review. Hydrobiologia 328, 215261.CrossRefGoogle Scholar
Turner, S.J., Thrush, S.F., Cummings, V.J., Hewitt, J.E., Wilkinson, M.R., Williamson, R.B. and Lee, D.J. (1997) Changes in epifaunal assemblages in response to marina operations and boating activities. Marine Environmental Research 43, 181199.CrossRefGoogle Scholar
Van Dolah, R.F., Bobo, M.Y., Levisen, M.V., Wendt, P. and Manzi, J. (1992) Effects of marina proximity on the physiological condition, reproduction, and settlement of oyster populations. Journal of Shellfish Research 11, 4148.Google Scholar
Weis, J.S. and Weis, P. (1992) Construction materials in estuaries: reduction in epibiotic community on chromated copper arsenate (CCA) treated wood. Marine Ecology Progress Series 83, 4553.Google Scholar
Wendt, P.H., Van Dolah, R.F., Bobo, M.Y. and Manzi, J.J. (1990) Effects of marina proximity on certain aspects of the biology of oysters and other benthic macrofauna in a South Carolina Estuary. South Carolina Wildlife and Resources Department, Charleston, SC, South Carolina Resources Center, Technical Report Number 74, 49 pp.Google Scholar
Weston, D.P. (1990) Quantitative examination of macrobenthic community changes along an organic enrichment gradient. Marine Ecology Progress Series 61, 233244.CrossRefGoogle Scholar