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Changes in the benthic community of china clay waste deposits in Mevagissey Bay following a reduction of discharges

Published online by Cambridge University Press:  11 May 2009

P. Keith Probert
P. Keith Probert
Affiliation:
Nature Conservancy Council, Godwin House, George Street, Huntingdon
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Extract

Macrobenthic infauna was sampled in Mevagissey Bay, off the south coast of Cornwall, England, when the bay was receiving fine-grained mineral waste from the china clay industry at a rate of about 450000 tons per annum. Quintuplicate 0·1 m2 grab samples, washed on a 0·5 mm mesh, were taken on 15 occasions over two years at a station about 1 km from the outfall and at a water depth of 13 m. The fauna had a range of density of 755–2144 individuals/0–5 m2 and in composition resembled a partially impoverished Echinocardium cordatum/Amphiurafiliformis community. Population densities of Goniada maculata (Polychaeta), Cingula semicostata (Gastropoda), Nucula turgida, Mysella bidentata, Venus striatula and Tellina fabula (Bivalvia) showed no clear trends during the two years' sampling. Magelona filiformis (Polychaeta), Abra alba and Phaxas pellucidus (Bivalvia), Acrocnida brachiata and Amphiura filiformis (Ophiuroidea) declined in abundance, whereas the densities of Nephtys hombergi (Polychaeta) and Labidoplax digitata (Holothurioidea) increased. L. digitata became the commonest species, with a peak density of 708 individuals/0·5 m2. A month after sampling began the rate of waste discharged was reduced from 700000 tons per annum, but this did not appear to improve conditions for the benthic community. Total faunal density remained relatively stable but species diversity declined. It is argued that the suspended solid concentration was unlikely to have adversely affected the predominantly deposit-feeding community, but that persistent sediment instability continued to be a source of stress. Nevertheless, the observed major changes of community structure were similar to natural fluctuations of coastal soft-bottom populations resulting from species interactions and differences of larval success.

Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 61 , Issue 3 , August 1981 , pp. 789 - 804
Copyright
Copyright © Marine Biological Association of the United Kingdom 1981

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References

Aller, R. C. & Dodge, R. E., 1974. Animal-sediment relations in a tropical lagoon, Discovery Bay, Jamaica. Journal of Marine Research, 32, 209–232.Google Scholar
Barel, C. D. N. & Kramers, P. G. N., 1977. A survey of the echinoderm associates of the north-east Atlantic area. Zoologische verhandelingen, 156, 159 pp.Google Scholar
Barnes, H., 1952. The use of transformations in marine biological statistics. Journal du Conseil, 18, 61–71.CrossRefGoogle Scholar
Bradfield, R. E. N., Kingsbury, R. W. S. M. & Rees, C. P., 1976. An assessment of the pollution of Cornish coastal waters. Marine Pollution Bulletin, 7, 187–193.CrossRefGoogle Scholar
Buchanan, J. B., 1971. Measurement of the physical and chemical environment. Sediments. In Methods for the Study of Marine Benthos (ed. Holme, N. A. and Mclntyre, A. D.), pp. 30–52. Oxford: Blackwell Scientific Publications.Google Scholar
Eagle, R. A., 1975. Natural fluctuations in a soft bottom benthic community. Journal of the Marine Biological Association of the United Kingdom, 55, 865–878.Google Scholar
Eagle, R. A., Hardiman, P. A., Norton, M. G. & Nunny, R. S., 1978. The field assessment of effects of dumping wastes at sea. 3. A survey of the sewage sludge disposal area in Lyme Bay. Technical Report of the Fisheries Laboratory, Lozvestoft, no. 49, 22 pp.Google Scholar
Gibbs, P. E. & Probert, K., 1973. Notes on Gyptis capensis and Sosane sulcata [Annelida: Polychaeta] from the benthos off the south coast of Cornwall. Journal of the Marine Biological Association of the United Kingdom, 53, 397–401.CrossRefGoogle Scholar
Green, D. W., 1972. An investigation of the disposal of micaceous residue through a sea outfall. Proceedings of the Institution of Civil Engineers, 53, 127–145.CrossRefGoogle Scholar
Hjulstrom, F., 1935. Studies of the morphological activity of rivers as illustrated by the River Fyris. III. Erosion, transportation and sedimentation. Bulletin of the Geological Institution of the University of Upsala, 25, 292–346.Google Scholar
Hollister, C. D. & Heezen, B. C, 1972. Geologic effects of ocean bottom currents: western North Atlantic. In Studies in Physical Oceanography, vol. 2 (ed. Gordon, A. L.), pp. 37–66. New York: Gordon & Breach.Google Scholar
Holme, N. A., 1953. The biomass of the bottom fauna in the English Channel off Plymouth. Journal of the Marine Biological Association of the United Kingdom, 32, 1–49.Google Scholar
Holme, N. A., 1966. The bottom fauna of the English Channel. Part II. Journal of the Marine Biological Association of the United Kingdom, 46, 401–493.Google Scholar
Holme, N. A. & Probert, P. K., 1978. Disposal of solid waste in the marine environment with particular reference to the china clay industry. In Environmental Management of Mineral Wastes (ed. Goodman, G. T. and Chadwick, M. J.), pp. 239–253. Netherlands: Sijthoff & Noordhoff.CrossRefGoogle Scholar
Howell, B. R. & Shelton, R. G. J., 1970. The effect of china clay on the bottom fauna of St Austell and Mevagissey Bays. Journal of the Marine Biological Association of the United Kingdom, 50, 593–607.Google Scholar
Kranz, P. M., 1974. The anastrophic burial of bivalves and its paleoecological significance. Journal of Geology, 82, 237–265.Google Scholar
Lloyd, M., Zar, J. H. & Karr, J. R., 1968. On the calculation of information-theoretical measures of diversity. American Midland Naturalist, 79, 257–272.CrossRefGoogle Scholar
Mccall, P. L., 1978. Spatial-temporal distributions of Long Island Sound infauna: the role of bottom disturbance in a nearshore marine habitat. In Estuarine Interactions (ed. Wiley, M. L.), pp. 191–219. New York: Academic Press.Google Scholar
Margalef, R., 1958. Information theory in ecology. General Systems, 3, 36–71.Google Scholar
Marine Biological Association, 1957. Plymouth Marine Fauna, 3rd edition, xlii, 457 pp. Plymouth.Google Scholar
Maurer, D., Leathem, W., Kinner, P. & Tinsman, J., 1979. Seasonal fluctuations in coastal benthic invertebrate assemblages. Estuarine and Coastal Marine Science, 8, 181–193.CrossRefGoogle Scholar
Moore, P. G., 1972. Paniculate matter in the sublittoral zone of an exposed coast and its ecological significance with special reference to the fauna inhabiting kelp holdfasts. Journal of Experi-mental Marine Biology and Ecology, 10, 59–80.Google Scholar
Newton, A. J. & Gray, J. S., 1972. Seasonal variation of the suspended solid matter, off the coast of North Yorkshire. Journal of the Marine Biological Association of the United Kingdom, 52, 33–47.CrossRefGoogle Scholar
Nichols, J. A., Rowe, G. T., Clifford, C. H. & Young, R. A., 1978. In situ experiments on the burial of marine invertebrates. Journal of Sedimentary Petrology, 48, 419–425.Google Scholar
Petersen, C. G. J., 1913. Valuation of the sea. II. The animal communities of the sea-bottom and their importance for marine zoogeography. Report of the Danish Biological Station to the Board of Agriculture, 21, 44 pp.Google Scholar
Portmann, J. E., 1970. The effect of china clay on the sediments of St Austell and Mevagissey Bays. Journal of the Marine Biological Association of the United Kingdom, 50, 577–591.Google Scholar
Powell, E. N., 1977. Particle size selection and sediment reworking in a funnel feeder, Leptosynapta tenuis (Holothurioidea, Synaptidae). Internationale Revue der gesamten Hydrobiologie, 62, 385–408.CrossRefGoogle Scholar
Probert, P. K., 1975. The bottom fauna of china clay waste deposits in Mevagissey Bay. Journal of the Marine Biological Association of the United Kingdom, 55, 19–44.Google Scholar
Rhoads, D. C., Yingst, J. Y. & Ullman, W. J., 1978. Seafloor stability in central Long Island Sound. Part I. Temporal changes in erodibility of fine-grained sediment. In Estuarine Interactions (ed. Wiley, M. L.), pp. 221–244. New York: Academic Press.Google Scholar
Rhoads, D. C. & Young, D. K., 1970. The influence of deposit-feeding organisms on sediment stability and community trophic structure. Journal of Marine Research, 28, 150–178.Google Scholar
Saila, S. B., 1976. Sedimentation and food resources: animal-sediment relationships. In Marine Sediment Transport and Environmental Management (ed. Stanley, D. J. and Swift, D. J. P.), pp. 479–492. New York: Wiley.Google Scholar
Sanders, H. L., 1979. Evolutionary ecology and life-history patterns in the deep sea. Sarsia, 64, 1–7.Google Scholar
Segerstrale, S. G., 1973. Results of bottom fauna sampling in certain localities in the Tvarminne area (inner Baltic), with special reference to the so-called Macoma-Pontoporeia theory. Commentationes biologicae, 67, 12 pp.Google Scholar
Thorson, G., 1946. Reproduction and larval development of Danish marine bottom invertebrates, with special reference to the planktonic larvae in the Sound (0resund). Meddelelser fra Kommissionen for Danmarks Fiskeri- og Havundersegelser (ser. Plankton), 4, 523 pp.Google Scholar
Thorson, G., 1950. Reproduction and larval ecology of marine bottom invertebrates. Biological Reviews, 25, 1–45.Google Scholar
Williams, C. B., 1950. The application of the logarithmic series to the frequency of occurrence of plant species in quadrats. Journal of Ecology, 38, 107–138.Google Scholar
Wilson, K. W. & Connor, P. M., 1976. The effect of china clay on the fish of St Austell and Mevagissey Bays. Journal of the Marine Biological Association of the United Kingdom, 56, 769–780.CrossRefGoogle Scholar
Winckworth, R., 1923. Montacuta bidentata (Montagu). Journal of Conchology, 17, 86.Google Scholar
Zenkevitch, L. A., 1963. Biology of the Seas of the U.S.S.R. (transl. by Botcharskaya, S.). 955 pp. London: Allen and Unwin.CrossRefGoogle Scholar
Ziegelmeier, E., 1970. Uber Massenvorkommen verschiedener makrobenthaler Wirbelloser wahrend der Wiederbesiedlungsphase nach Schadigungen durch ‘ katastrophale’ Umwelteinfliisse. Helgolander wissenschaftliche Meeresuntersuchungen, 21, 9—20.Google Scholar
Ziegelmeier, E., 1978. Macrobenthos investigations in the eastern part of the German Bight from 1950 to 1974. Rapport et proces-verbaux des reunions. Conseil international pour Vexploration de la mer, 172, 432–444.Google Scholar