Hostname: page-component-8448b6f56d-wq2xx Total loading time: 0 Render date: 2024-04-19T19:00:10.169Z Has data issue: false hasContentIssue false

Uptake, tissue distribution and metabolism of 14C-labelled tributyltin (TBT) in the dog-whelk, Nucella lapillus

Published online by Cambridge University Press:  11 May 2009

G. W. Bryan
Affiliation:
Plymouth Marine Laboratory, Citadel Hill, Plymouth, PL1 2PB.
D. A. Bright
Affiliation:
Environmental Sciences Group, Royal Roads Military College, MFO Victoria, British Columbia, VOS 1B0, Canada
L. G. Hummerstone
Affiliation:
Plymouth Marine Laboratory, Citadel Hill, Plymouth, PL1 2PB.
G. R. Burt
Affiliation:
Plymouth Marine Laboratory, Citadel Hill, Plymouth, PL1 2PB.

Extract

A study of tributyltin (TBT) uptake, tissue distribution and breakdown in dog-whelks, Nucella lapillus, was carried out using 14C-labelled tributyltin chloride. The compound was introduced into animals by exposure to sea-water, from a diet of labelled mussels and by injection. Measurements of 14C were made on tissue extracts containing total 14C, TBT+DBT and TBT. Organs examined included digestive gland, kidney, mantle, foot, viscera, gonads and blood. Absorption of dissolved TBT occurred primarily via tissues associated with the mantle: autoradiographic evidence showed that of these the ctenidium (gill) and osphradium were probably most important. Of non-reproductive tissues, mantle displayed least evidence of TBT degradation whereas kidney and digestive gland contained lower proportions of 14C as TBT (~60%) than other tissues. By virtue of its more rapid response, initially at least, the kidney had a primary role in degrading dissolved TBT that reached the blood. Dog-whelks feeding on labelled Mytilus edulis absorbed organotins very efficiently via the digestive gland, which then played a major role in TBT breakdown. However, the capacity for degradation is not sufficient to prevent, TBT concentration factors of the order of 100,000 (dry tissue/water) being attained in N. lapillus. Autoradiography revealed surprisingly high grain-counts in nerves, which may be significant in view of evidence in the literature that neurohormones are intermediaries in the chain linking TBT with imposex.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 1993

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

Bright, D.A. & Ellis, D. V., 1990. A comparative survey of imposex in north-east Pacific neogastropods (Prosobranchia) related to tributyltin contamination, and choice of a suitable bioindicator. Canadian Journal of Zoology, 68, 19151924.CrossRefGoogle Scholar
Bryan, G.W. & Gibbs, P.E., 1991. Impact of low concentrations of tributyltin (TBT) on marine organisms: a review. In Metal ecotoxicology: concepts and applications (ed. M.C., Newman and A.W., Mclntosh), pp. 323361. Ann Arbor: Lewis Publishers.Google Scholar
Bryan, G.W., Gibbs, P.E. & Burt, G.R., 1988. A comparison of the effectiveness of tri-n-butyltin chloride and five other organotin compounds in promoting the development of imposex in the dog-whelk, Nucella lapillus. Journal of the Marine Biological Association of the United Kingdom, 68, 733744.CrossRefGoogle Scholar
Bryan, G.W., Gibbs, P.E., Burt, G.R. & Hummerstone, L.G., 1987. The effects of tributyltin (TBT) accumulation on adult dog-whelks, Nucella lapillus: long-term field and laboratory experiments. Journal of the Marine Biological Association of the United Kingdom, 67, 525544.CrossRefGoogle Scholar
Bryan, G.W., Gibbs, P.E., Hummerstone, L.G. & Burt, G.R., 1986. The decline of the gastropod Nucella lapillus around south-west England: evidence for the effect of tributyltin from antifouling paints. Journal of the Marine Biological Association of the United Kingdom, 66, 611640.CrossRefGoogle Scholar
Bryan, G.W., Gibbs, P.E., Hummerstone, L.G. & Burt, G.R., 1989. Uptake and transformation of re labelled tributyltin chloride by the dog-whelk, Nucella lapillus: importance of absorption from the diet. Marine Environmental Research, 28, 241245.CrossRefGoogle Scholar
Ellis, D.V. & Pattisina, L.A., 1990. Widespread neogastropod imposex: a biological indication of global TBT contamination? Marine Pollution Bulletin, 21, 248253.CrossRefGoogle Scholar
Fent, K., 1991. Bioconcentration and elimination of tributyltin chloride by embryos and larvae of minnows Phoxinus phoxinus. Aquatic Toxicology, 20, 147158.CrossRefGoogle Scholar
Fent, K. & Hunn, J., 1993. Uptake and elimination of tributyltin in fish yolk-sac larvae. Marine Environmental Research, 35, 6571.CrossRefGoogle Scholar
Fent, K. & Stegeman, J.J., 1991. Effects of tributyltin chloride in vitro on the hepatic microsomal monooxygenase system in the fish Stenotomus chrysops. Aquatic Toxicology, 20, 159168.CrossRefGoogle Scholar
Fent, K. & Stegeman, J.J., 1993. Effects of tributyltin in vivo on hepatic cytochrome P450 forms in marine fish. Aquatic Toxicology, 24, 219240.CrossRefGoogle Scholar
Feral, C., & Le Gall, S., 1983. The influence of a pollutant factor (tributyltin) on the neuroendocrine mechanism responsible for the occurrence of a penis in the females of Ocenebra erinacea. In Molluscan neuro-endocrinology: Proceedings of the International Minisymposium on Molluscan Endocrinology (ed. I., Lever and H.H., Boer), pp. 173175. Amsterdam: North Holland.Google Scholar
Francois, R., Short, F.T. & Weber, J.H., 1989. Accumulation and persistence of tributyltin in eelgrass (Zostera marina L.) tissue. Environmental Science and Technology, 23, 191196.CrossRefGoogle Scholar
Gibbs, P.E., Pascoe, P.L. & Burt, G.R., 1988. Sex change in the female dog-whelk, Nucella lapillus, induced by tributyltin from antifouling paints. Journal of the Marine Biological Association of the United Kingdom, 68, 715731,CrossRefGoogle Scholar
Humason, G.L., 1967. Animal tissue techniques. London: W.H. Freeman.Google Scholar
Langston, W.J., Burt, G.R. & Mingjiang, Zhou, 1987. Tin and organotin in water, sediment, and benthic organisms of Poole Harbour. Marine Pollution Bulletin, 18, 634639.CrossRefGoogle Scholar
Lee, R.F., 1985. Metabolism of tributyltin oxide by crabs, oysters and fish. Marine Environmental Research, 17, 145148.CrossRefGoogle Scholar
Lee, R.F., 1986. Metabolism of bis(tributyltin)oxide by estuarine animals. In Oceans ‘86 Proceedings. Vol 4. International Organotin Symposium, pp. 11821188. New York: Institute of Electrical and Electronics Engineers.Google Scholar
Lee, R.F., 1989. Metabolism and accumulation of xenobiotics within hepato-pancreas cells of the blue crab, Callinectes sapidus. Marine Environmental Research, 28, 9397.CrossRefGoogle Scholar
Lee, R.F., 1991. Metabolism of tributyltin by marine animals and possible linkages to effects. Marine Environmental Research, 32, 2935.CrossRefGoogle Scholar
Lee, R.F., Valkirs, A.O. & Seligman, P.F., 1989. Importance of microalgae in the biodegradation of tributyltin in estuarine waters. Environmental Science and Technology, 23, 15151518.CrossRefGoogle Scholar
Livingstone, D.R., 1991. Organic xenobiotic metabolism in marine invertebrates. Advances in Comparative and Environmental Physiology, 7, 45185.CrossRefGoogle Scholar
Livingstone, D.R. & Farrar, S.V., 1985. Responses of the mixed function oxidase system of some bivalve and gastropod molluscs to exposure to polynuclear aromatic and other hydrocarbons. Marine Environmental Research, 17, 101105.CrossRefGoogle Scholar
Martin, R.C., Dixon, D.G., Maguire, R.J., Hodson, P.V. & Tkacz, R.J., 1989. Acute toxicity, uptake, depuration and tissue distribution of tri-n-butyltin in rainbow trout Salmo gairdneri. Aquatic toxicology, 15, 3752.CrossRefGoogle Scholar
Rice, S.D., Short, J. W. & Stickle, W.B., 1989. Uptake and catabolism of tributyltin by blue crabs fed TBT-contaminated prey. Marine Environmental Research, 27, 137145.CrossRefGoogle Scholar
Rogers, A.W., 1967. Techniques of autoradiography. Amsterdam: Elsevier.Google Scholar
Schultze, B., 1969. Physical techniques in biological research, 2nd ed. Vol. Ill, Part B. Autoradiography at the cellular level (ed. A.W., Pollister), pp. 1301. New York: Academic Press.Google Scholar
Smith, B.S., 1981. Tributyltin compounds induce male characteristics on female mud snails Nassarius obsoletus = Ilyanassa obsoleta. Journal of Applied Toxicology, 1, 141144.CrossRefGoogle ScholarPubMed
Spooner, N., Gibbs, P.E., Bryan, G.W. & Goad, L.J., 1991. The effect of tributyltin upon steroid titres in the female dog-whelk, Nucella lapillus, and the development of imposex. Marine Environmental Research, 32, 3749.CrossRefGoogle Scholar
Stickle, W.B., Sharp-Dahl, J.L., Rice, S.D. & Short, J.W., 1990. Imposex induction in Nucella lima (Gmelin) via mode of exposure to tributyltin. Journal of Experimental Marine Biology and Ecology, 143, 165180.CrossRefGoogle Scholar
Thain, J.E., Waldock, M.J. & Waite, M.E., 1987. Toxicity and degradation studies of tributyltin (TBT) and dibutyltin (DBT) in the aquatic environment. In Oceans ’87 Proceedings. Vol. 4. International Organotin Symposium, pp. 13981404. New York: Institute of Electrical and Electronics Engineers.Google Scholar