Abstract
Juveniles of the dendrobranchiate decapod Penaeus indicus take up radiolabelled zinc from solution at all exposure concentrations studied from 5.6 to 100 μg l−1, with an uptake rate constant of 0.045 l g−1 day−1 at 15 salinity and 25°C. Over the first 10 days of zinc exposure, the new zinc taken up is added to the existing zinc content of the prawn with no significant excretion; over this period the rate of accumulation of radiolabelled zinc is a measure of the absolute zinc uptake rate from solution. Over the next 10 days of zinc exposure to 10 μg Zn l−1, however, zinc is excreted at about half the rate of uptake resulting in a raised body concentration of zinc. Moulting had no significant effect on the accumulation of zinc. Newly accumulated zinc is distributed to all organs with the highest proportions of body content being found in the exoskeleton, followed by the muscle, the hepatopancreas and the antennal organs. Radiolabelled zinc is subsequently lost from all organs. Unlike caridean shrimps or prawns (pleocyemate decapods), therefore, penaeids (dendrobranchiate decapods) do not show regulation of zinc body concentrations to a constant level over a range of dissolved zinc bioavailabilities by matching zinc excretion to zinc uptake. Nevertheless, unlike amphipod crustaceans, P. indicus does excrete some of the zinc newly accumulated from solution after a time delay. Unlike their caridean counterparts, penaeid prawns inhabiting anthropogenically contaminated coastal waters with raised zinc bioavailabilities can be expected to contain raised body concentrations of zinc.
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References
Al-Mohanna SY, Nott JA (1985) The accumulation of metals in the hepatopancreas of the shrimp Penaeus semisulcatus de Haan (Crustacea: Decapoda) during the moult cycle. In: Halwagy R, Clayton D, Behbehani, M (eds) Marine Environment and Pollution, Proc 1st Arabian Gulf Conference on Environment and Pollution. University of Kuwait, Kuwait, pp 195–207
Bryan GW (1968) Concentrations of zinc and copper in the tissues of decapod crustaceans. J Mar Biol Assoc UK 48:303–321
Bryan GW (1976) Some aspects of heavy metal tolerance in aquatic organisms. In: Lockwood APM (ed) Effects of pollutants on aquatic organisms. Cambridge University Press, London, pp 7–34
Bryan GW, Langston WJ, Hummerstone LG, Burt GR (1985) A guide to the assessment of heavy-metal contamination in estuaries using biological indicators. Occas Publ Mar Biol Assoc UK 4:1–92
Chinni S, Yallapragada PR (2000) Toxicity of copper, cadmium, zinc and lead to Penaeus indicus postlarvae: effects of individual metals. J Environ Biol 21:255–258
Dall W, Moriarty DJ (1983) Functional aspects of nutrition and digestion. In: Mantel LH (ed) The biology of Crustacea, Internal anatomy and physiological regulation. Academic, New York, pp 215–261
Devineau J, Amiard-Triquet C (1985) Patterns of bioaccumulation of an essential trace element (zinc) and a pollutant metal (cadmium) in larvae of the prawn Palaemon serratus. Mar Biol 86:139–143
Eisler R (1981) Trace metal concentrations in marine organisms. Pergamon, Oxford
Galay Burgos M, Rainbow PS (1998) Uptake, accumulation and excretion by Corophium volutator (Crustacea: Amphipoda) of zinc, cadmium and cobalt added to sewage sludge. Estuar Coastal Shelf Sci 47:603–620
Gibson R, Barker PL (1979) The decapod hepatopancreas. Oceanogr Mar Biol Annu Rev 17:285–346
Grey DL, Dall W, Baker A (1983) A Guide to the Australian Penaeid Prawns. Northern Territory, Darwin, Australia
Holthuis LB (1980) FAO species catalogue, vol 1. Shrimps and prawns of the world. An annotated catalogue of species of interest to fisheries. Food and Agriculture Organization of the United Nations, Rome
Joseph KO, Srivastava JP, Kadir PMA (1992) Acute toxicity of five heavy metals to the prawn, Penaeus indicus H. Milne Edwards in brackishwater medium. J Inland Fish Soc India 24:82–84
Law RJ, Waldock MJ, Allchin CR, Laslett RE, Bailey KJ (1994) Contaminants in seawater around England and Wales: results from monitoring surveys, 1990–1992. Mar Pollut Bull 28:668–675
Le Reste L (1978) Biologie d’une population de crevettes Penaeus indicus H. Milne Edwards sur la cote nord-ouest de Madagascar. ORSTOM, Paris
Luoma SN, Rainbow PS (2005) Why is metal bioaccumulation so variable? Biodynamics as a unifying concept. Environ Sci Technol (in press)
Masala O, O’Brien P, Rainbow PS (2004) Analysis of metal-containing granules in the barnacle Tetraclita squamosa. J Inorg Biochem 98:1095–1102
McLaughlin PA (1983) Internal anatomy. In: Mantel LH (ed) The biology of Crustacea. Internal anatomy and physiological regulation. Academic, New York, pp 1–53
Nugegoda D, Rainbow PS (1988) Zinc uptake and regulation by the sublittoral prawn Pandalus montagui (Crustacea: Decapoda). Estuar Coastal Shelf Sci 26:619–632
Nugegoda D, Rainbow PS (1989) Effects of salinity changes on zinc uptake and regulation by the decapod crustaceans Palaemon elegans and Palaemonetes varians. Mar Ecol Prog Ser 51:57–75
Paez-Osuna F, Bojorquez-Mascareno E (2002) Concentración y distribución de metales pesados de los camarones Litopenaeus vannamei y L. stylirostris del Sureste del Golfo de California. In: Hendrickx ME (eds) Universidad Nacional Autónoma de México Mazatlán, Sin, pp 293–300
Paez-Osuna F, Frias-Espiricueta MG (2001) Bioacumulación, distribución y efectos de los metales pesados en los peneidos. In: Paez-Osuna F (ed) Acualcutura y medio ambiente. UAS, Mazatlán, México, pp 277–311
Paez-Osuna F, Ruiz-Fernandez C (1995a) Trace metals in the Mexican shrimp Penaeus vannamei from estuarine and marine environments. Environ Pollut 87:243–247
Paez-Osuna F, Ruiz-Fernandez C (1995b) Comparative bioaccumulation of trace metals in Penaeus stylirostris in estuarine and coastal environments. Estuar Coastal Shelf Sci 40:35–44
Paez-Osuna F, Tron-Mayen L (1995) Distribution of heavy metals in tissues of the shrimp Penaeus californiensis from the Northwest coast of Mexico. Bull Environ Contam Toxicol 55:209–215
Pérez-Farfante I, Kensley B (1997) Penaeoid and sergestoid shrimps and prawns of the world. Mémoires du Museum National d’Histoire Naturelle, Paris 175
Pullen JSH, Rainbow PS (1991). The composition of pyrophosphate heavy metal detoxification granules in barnacles. J Exp Mar Biol Ecol 150:249–266
Rainbow PS (1990) Heavy metal levels in marine invertebrates. In: Furness RW, Rainbow PS (eds) Heavy metals in the marine environment. CRC, Boca Raton, pp 67–79
Rainbow PS (1993) The significance of trace metal concentrations in marine invertebrates. In: Dallinger R, Rainbow PS (eds) Ecotoxicology of metals in invertebrates. Lewis, Boca Raton, pp 3–23
Rainbow PS (1997) Ecophysiology of trace metal uptake in crustaceans. Estuar Coastal Shelf Sci 44:169–175
Rainbow PS (1998) Phylogeny of trace metal accumulation in crustaceans. In: Langston WJ Bebianno MJ (Eds) Metal metabolism in aquatic environments. Chapman and Hall, London, pp 285–319
Rainbow PS (2002). Trace metal concentrations in aquatic invertebrates: why and so what? Environ Pollut 120:497–507
Rainbow PS, Wang W-X (2001) Comparative assimilation of Cd, Cr, Se, and Zn by the barnacle Elminius modestus from phytoplankton and zooplankton diets. Mar Ecol Prog Ser 218:239–248
Rainbow PS, White SL (1989) Comparative strategies of heavy metal accumulation by crustaceans: zinc, copper and cadmium in a decapod, an amphipod and a barnacle. Hydrobiologia 174:245–262
Rainbow PS, White SL (1990) Comparative accumulation of cobalt by three crustaceans: a decapod, an amphipod and a barnacle. Aquat Toxicol 16:113–126
Rainbow PS, Blackmore G, Wang W-X (2003) Effects of previous field-exposure history on the uptake of trace metals from water and food by the barnacle Balanus amphitrite. Mar Ecol Prog Ser 259:201–203
Vogt G, Quinitio ET (1994) Accumulation and excretion of metal granules in the prawn, Penaeus monodon , exposed to water-borne copper, lead, iron and calcium. Aquat Toxicol 28:223–241
Weeks JM, Rainbow PS (1991) The uptake and accumulation of zinc and copper from solution by two species of talitrid amphipods (Crustacea). J Mar Biol Ass U.K. 71:811–826
White SL, Rainbow PS (1982). Regulation and accumulation of copper, zinc and cadmium by the shrimp Palaemon elegans. Mar Ecol Prog Ser 8:95–101
White SL, Rainbow PS (1984a) Regulation of zinc concentration by Palaemon elegans (Crustacea: Decapoda): zinc flux and effects of temperature, zinc concentration and moulting. Mar Ecol Prog Ser 16:135–147
White SL, Rainbow PS (1984b) Zinc flux in Palaemon elegans (Crustacea: Decapoda): Moulting, individual variation and tissue distribution. Mar Ecol Prog Ser 19:153–166
Acknowledgements
This work was supported by funding to G.N.-N. from CONACyT and SEP-Mexico. It is a pleasure to acknowledge the considerable technical support of Brian Smith and Alan Scott.
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Communicated by J.P. Thorpe, Port Erin
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Nunez-Nogueira, G., Rainbow, P. Kinetics of zinc uptake from solution, accumulation and excretion by the decapod crustacean Penaeus indicus. Marine Biology 147, 93–103 (2005). https://doi.org/10.1007/s00227-004-1542-0
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DOI: https://doi.org/10.1007/s00227-004-1542-0