Hostname: page-component-78c5997874-t5tsf Total loading time: 0 Render date: 2024-11-20T04:08:40.921Z Has data issue: false hasContentIssue false

Copper accumulation by the polychaete Melinna palmata: an antipredation mechanism?

Published online by Cambridge University Press:  11 May 2009

P. E. Gibbs
Affiliation:
The Laboratory, Marine Biological Association, Citadel Hill, Plymouth
G. W. Bryan
Affiliation:
The Laboratory, Marine Biological Association, Citadel Hill, Plymouth
K. P. Ryan
Affiliation:
The Laboratory, Marine Biological Association, Citadel Hill, Plymouth

Extract

Analyses of the ampharetid polychaete Melinna palmata have shown that this species consistently contains a high concentration of copper. The related species Melinna cristata also has a high copper content but Ampharete acutifrons and Amphicteis gunneri have low copper contents. M. palmata usually contains copper in concentrations in excess of 600 μg/g (dry weight) and often above 1100 μg/g; much of this copper is embodied in the branchiae which have concentrations of 0·4–1·2% copper and, although these organs account for only 3–4% of the dry body weight, their copper content represents 30–40% of the total body burden. X-ray microanalysis shows the copper in the branchiae to be concentrated in special epidermal cells. The function of the copper in these cells does not appear to be associated with detoxication, luminescence or an antifouling mechanism but feeding trials have shown the branchiae of Melinna palmata, but not of Ampharete acutifrons, to be distasteful to certain small fish. Thus it is thought the copper may reduce the palatability of the tissues and is accumulated by Melinna palmata as a chemical defence against predation.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 1981

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

Bellisario, R. & Cormier, M. J., 1971. Peroxide-linked bioluminescence catalyzed by a copper-containing, non-heme luciferase isolated from a bioluminescent earthworm. Biochemical and Biophysical Research Communications, 43, 800805.CrossRefGoogle ScholarPubMed
Bellisario, R., Spencer, T. E. & Cormier, M. J., 1972. Isolation and properties of luciferase, a non-heme peroxidase, from the bioluminescent earthworm, Diplocardia longa. Biochemistry, 11, 22562266.CrossRefGoogle ScholarPubMed
Bryan, G. W., 1976. Heavy metal contamination in the sea. In Marine Pollution (ed. R., Johnston), pp. 185302. London: Academic Press.Google Scholar
Bryan, G. W. & Gibbs, P. E., 1979. Zinc - a major inorganic component of nereid polychaete jaws. Journal of the Marine Biological Association of the United Kingdom, 59, 969973.CrossRefGoogle Scholar
Bryan, G. W. & Gibbs, P. E., 1980. Metals in nereid polychaetes: the contribution of metals in the jaws to the total body burden. Journal of the Marine Biological Association of the United Kingdom, 60, 641654.CrossRefGoogle Scholar
Bryan, G. W. & Hummerstone, L. G., 1971. Adaptation of the polychaete Nereis diversicolor to estuarine sediments containing high concentrations of heavy metals. I. General observations and adaptation to copper. Journal of the Marine Biological Association of the United Kingdom, 51, 845863.CrossRefGoogle Scholar
Day, J. H., 1964. A review of the Family Ampharetidae (Polychaeta). Annals of the South African Museum, 48, 97120.Google Scholar
Fauchald, K., 1977. The polychaete worms: definitions and keys to the orders, families and genera. Science Series. Natural History Museum of Los Angeles County, 28, 188 pp.Google Scholar
George, S. G., Pirie, B. J. S., Cheyne, A. R., Coombs, T. L. & Grant, P. T., 1978. Detoxication of metals by marine bivalves: an ultrastructural study of the compartmentation of copper and zinc in the oyster Ostrea edulis. Marine Biology, 45, 147156.CrossRefGoogle Scholar
Gibbs, P. E. & Bryan, G. W., 1980. Copper - the major metal component of glycerid polychaete jaws. Journal of the Marine Biological Association of the United Kingdom, 60, 205214.CrossRefGoogle Scholar
Henry, J. P., Monny, C. & Michelson, A. M., 1975. Characterization and properties of Pholas luciferase as a metalloglycoprotein. Biochemistry, 14, 34583466.CrossRefGoogle ScholarPubMed
Nicol, J. A. C, 1952. Studies on Chaetopterus variopedatus (Renier). II. Nervous control of light production. Journal of the Marine Biological Association of the United Kingdom, 30, 433452.CrossRefGoogle Scholar
Pearse, A. G. E., 1972. Histochemistry: Theoretical and Applied, 3rd ed. vol. 2. 7611518 pp. Edinburgh: Churchill Livingstone.Google Scholar
Prezant, R. S., 1980. An antipredation mechanism of the polychaete Phyllodoce mucosa with notes on similar mechanisms in other potential prey. Fishery Bulletin. National Oceanic and Atmospheric Administration of the United States, 77, 605616.Google Scholar
Retiere, C, 1979. Contribution a la Connaissance des Peuplements Benthiques du Golfe Normanno-breton. Thése, Universitite de Rennes.Google Scholar
Stoecker, D., 1980. Relationships between chemical defense and ecology in benthic ascidians. Marine Ecology-Progress Series, 3, 257265.CrossRefGoogle Scholar
Thompson, T. E., 1960. Defensive acid-secretion in marine gastropods. Journal of the Marine Biological Association of the United Kingdom, 39, 115122.CrossRefGoogle Scholar
Whittaker, R. H. & Feeny, P. P., 1971. Allelochemics: chemical interactions between species. Science, New York, 171, 757770.CrossRefGoogle ScholarPubMed
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, 769780.CrossRefGoogle Scholar