Integrating lipids and contaminants in aquatic ecology and ecotoxicology

  • Martin J. Kainz
  • Aaron T. Fisk


Heterotrophic organisms in marine and freshwater food webs ingest a wide range of essential and xenobiotic compounds. Essential compounds are physiologically required by consumers, yet cannot be synthesized de novo, or cannot be synthesized in quantities sufficient to meet an organism’s need for somatic growth, reproduction, and survival (see Goulden and Place 1990, for daphnids; Tocher 2003, for teleost fishes). For example, some polyunsaturated fatty acids (PUFA) and trace elements such as zinc (Zn), iron (Fe), calcium (Ca) are considered essential, and if inadequate amounts are available in the diet, the health and fitness of an organism can be reduced. Xenobiotic compounds have no physiological value for organisms, but can be accumulated by consumers and can be toxic in cases were concentrations are sufficiently high (Watson et al. – Chap. 4). Xenobiotic compounds include many of the classic contaminants, such as PCBs, DDT, and mercury (Hg), and more recently recognized contaminants, such as estradiol, and can also be accumulated from non-dietary sources. It should be noted that essential compounds can also be toxic if concentrations are high enough or if they are converted to other molecules. For example, it has been suggested that PUFA in diatoms can be converted to unsaturated aldehydes, which reduce egg hatching rates in marine herbivorous copepods (Miralto et al. 1999).


Aquatic Organism High Trophic Level Trophic Position MeHg Concentration Xenobiotic Compound 
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  1. Ahlgren, G., Blomqvist, P., Boberg, M., and Gustafsson, I.B. 1994. Fatty acid content of the dorsal muscle – an indicator of fat quality in freshwater fish. J. Fish Biol. 45:131–157.Google Scholar
  2. Bec, A., Martin-Creuzburg, D., and von Elert, E. 2006. Trophic upgrading of autotrophic picoplankton by the heterotrophic nanoflagellate Paraphysomonas sp. Limnol. Oceanogr. 51:1699–1707.Google Scholar
  3. Bergen, B.J., Nelson, W.G., Quinn, J.G., and Jayaraman, S. 2001. Relationships among total lipid, lipid classes, and polychlorinated biphenyl concentrations in two indigenous populations of ribbed mussels (Geukensia demissa) over an annual cycle. Environ. Toxicol. Chem. 20:575–581.PubMedGoogle Scholar
  4. Borgå, K., Fisk, A.T., Hoekstra, P.F., and Muir, D.C.G. 2004. Biological and chemical factors of importance in the bioaccumulation and trophic transfer of persistent organochlorine contaminants in arctic marine food webs. Environ. Toxicol. Chem. 23:2367–2385.PubMedGoogle Scholar
  5. Brett, M. T., Müller-Navarra, D. C., Ballantyne, A. P., Ravet, J. L., and Goldman, C. R. 2006. Daphnia fatty acid composition reflects that of their diet. Limnol. Oceanogr. 51:2428–2437.Google Scholar
  6. Broman, D., Näf, C., Rolff, C., Zebuhr, Y., Fry, B., and Hobbie, J. 1992. Using ratios of stable nitrogen isotopes to estimate bioaccumulation and flux of polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) in two food chains from the northern Baltic. Environ. Toxicol. Chem. 11:331–345.Google Scholar
  7. Buckman, A.H., Brown, S.B., Small, J.M., Muir, D.C.G., Parrott, J.L., Solomon, K.R., and Fisk, A.T. 2007. The role of temperature and enzyme induction in the biotransformation of PCBs and bioformation of OH-PCBs by rainbow trout (Oncorhynchus mykiss). Environ. Sci. Technol. 41:3856–3863.PubMedGoogle Scholar
  8. Burreau, S., Axelman, J., Broman, D., and Jakobsson, E. 1997. Dietary uptake in pike (Esox lucius) of some polychlorinated biphenyls, polychlorinated naphthalenes and polybrominated diphenyl ethers administered in natural diet. Environ. Toxicol. Chem. 16:2508–2513.Google Scholar
  9. Cabana, G., and Rasmussen, J.B. 1994. Modelling food chain structure and contaminant bioaccumulation using stable nitrogen isotopes. Nature 372:255–257.Google Scholar
  10. Campbell, L.M., Schindler, D.W., Muir, D.C.G., Donald, D.B., and Kidd, K.A. 2000. Organochlorine transfer in the food web of subalpine Bow Lake, Banff National Park. Can. J. Fish. Aquat. Sci. 57:1258–1269.Google Scholar
  11. Campbell, L.M., Norstrom, R.J., Hobson, K.A., Muir, D.C.G., Backus, S., and Fisk, A.T. 2005a. Mercury and other trace elements in a pelagic Arctic marine food web (Northwater Polynya, Baffin Bay). Sci. Total Environ. 351:247–263.Google Scholar
  12. Campbell, L.M., Fisk, A.T., Wang, X., Köck, G., and Muir, D.C.G. 2005b. Evidence of biomagnification of rubidium in aquatic and marine food webs. Can. J. Fish. Aquat. Sci. 62: 1161–1167.Google Scholar
  13. Campfens, J., and MacKay, D. 1997. Fugacity-based model of PCB bioaccumulation in complex aquatic food webs. Environ. Sci. Technol. 31:577–583.Google Scholar
  14. Chu, F.L.E., Soudant, P., and Hall, R.C. 2003. Relationship between PCB accumulation and reproductive output in conditioned oysters Crassostrea virginica fed a contaminated algal diet. Aquat. Toxicol. 65:293–307.PubMedGoogle Scholar
  15. Copeman, L.A., Parrish, C.C., Brown, J.A., and Harel, M. 2002. Effects of docosahexaenoic, eicosapentaenoic, and arachidonic acids on the early growth, survival, lipid composition and pigmentation of yellowtail flounder (Limanda ferruginea): a live food enrichment experiment. Aquaculture 210:285–304.Google Scholar
  16. Countway, R.E., Dickhut, R.M., and Canuel, E.A. 2003. Polycyclic aromatic hydrocarbon (PAH) distributions and associations with organic matter in surface waters of the York River, VA Estuary. Org. Geochem. 34:209–224.Google Scholar
  17. Cunnane, S.C. 2003. Problems with essential fatty acids: time for a new paradigm? Prog. Lipid Res. 42:544–568.Google Scholar
  18. D’Adamo, R., Pelosi, S., Trotta, P., and Sansone, G. 1997. Bioaccumulation and biomagnification of polycyclic aromatic hydrocarbons in aquatic organisms. Mar. Chem. 56:45–49.Google Scholar
  19. Dalsgaard, J., St. John, M., Kattner, G., Müller-Navarra, D.C., and Hagen, W. 2003. Fatty acid trophic markers in the pelagic marine environment, pp. 225–340. In A.J. Southward, P.A Tyler, C.M. Young, C.M. Fuiman and L.A. [eds.], Advances in marine biology. Elsevier, Amsterdam.Google Scholar
  20. DeMott, W.R., Gulati, R.D., and Van Donk, E. 2001. Daphnia food limitation in three hypereutrophic Dutch lakes: Evidence for exclusion of large-bodied species by interfering filaments of cyanobacteria. Limnol. Oceanogr. 46:2054–2060.Google Scholar
  21. Dey, I., Buda, C., Wiik, T., Halver, J.E., and Farkas, T. 1993. Molecular and structural composition of phospholipid-membranes in livers of marine and freshwater fish in relation to temperature. Proc. Natl. Acad. Sci. USA 90:7498–7502.PubMedGoogle Scholar
  22. Dietz, R., Riget, F., and Johansen, P. 1996. Lead, cadmium, mercury and selenium in Greenland marine animals. Sci. Total Environ. 186:67–93.PubMedGoogle Scholar
  23. Duffus, J.H. 2002. “Heavy metals”-a meaningless term? IUPAC Technical Report. Pure Appl. Chem. 74:793–807.Google Scholar
  24. Ederington, M.C., McManus, G.B., and Harvey, H.R. 1995. Trophic transfer of fatty acids, sterols, and a triterpenoid alcohol between bacteria, a ciliate, and the copepod Acartia tonsa. Limnol. Oceanogr. 40:860–867.Google Scholar
  25. Engstrom-Ost, J., Lehtiniemi, M., Jonasdottir, S.H., and Viitasalo, M. 2005. Growth of pike larvae (Esox lucius) under different conditions of food quality and salinity. Ecol. Freshw. Fish 14:385–393.Google Scholar
  26. Evjemo, J.O., Reitan, K.I., and Olsen, Y. 2003. Copepods as live food organisms in the larval rearing of halibut larvae (Hippoglossus hippoglossus L.) with special emphasis on the nutritional value. Aquaculture 227:191–210.Google Scholar
  27. Finizio, A., Vighi, M., and Sandroni, D. 1997. Determination of N-octanol/water partition coefficient (Kow) of pesticide critical review and comparison of methods. Chemosphere 34:131–161.Google Scholar
  28. Fisher, N.S., Stupakoff, I., Sanudo-Wilhelmy, S., Wang, W.X., Teyssie, J.L., Fowler, S.W., and Crusius, J. 2000. Trace metals in marine copepods: a field test of a bioaccumulation model coupled to laboratory uptake kinetics data. Mar. Ecol. Prog. Ser. 194:211–218.Google Scholar
  29. Fisk, A.T., and Johnston, T.A. 1998. Maternal transfer of organochlorines to eggs of walleye (Stizostedion vitreum) in Lake Manitoba and western Lake Superior. J. Great Lakes Res. 24:917–928.Google Scholar
  30. Fisk, A.T., Norstrom, R.J., Cymbalisty, C.D., and Muir, D.C.G. 1998. Dietary accumulation and depuration of hydrophobic organochlorines: Bioaccumulation parameters and their relationship with the octanol/water partition coefficient. Environ. Toxicol. Chem. 17:951–961.Google Scholar
  31. Fisk, A.T., Tomy, G.T., Cymbalisty, C.D., and Muir, D.C.G. 2000. Dietary accumulation and QSARs for depuration and biotransformation of short (C10), medium (C14) and long (C18) carbon chain polychlorinated alkanes by juvenile rainbow trout (Oncorhynchus mykiss). Environ. Toxicol. Chem. 19:1508–1516.Google Scholar
  32. Fisk, A.T, Hobson, K.A, and Norstrom, R.J. 2001. Influence of chemical and biological factors on trophic transfer of persistent organic pollutants in the Northwater Polynya food web. Environ. Sci. Technol. 35:732–738.PubMedGoogle Scholar
  33. Fisk, A.T., Hoekstra, P.F., Gagnon, J-M., Norstrom, R.J., Hobson, K.A., Kwan, M., and Muir, D.C.G. 2003. Biological characteristics influencing organochlorine contaminants in Arctic marine invertebrates. Mar. Ecol. Prog. Ser. 262:201–214.Google Scholar
  34. Fox K., Zauke, G.-P., and Butte, W. 1994. Kinetics of bioconcentration and clearance of 28 polychlorinated biphenyl congeners in zebrafish (Brachydanio rerio). Ecotox. Environ. Safety 28:99–109.Google Scholar
  35. Gobas, F.A.P.C., McCorouodale, J.R., and Haffner, G.D. 1993. Intestinal-absorption and biomagnification of organochlorines. Environ. Toxicol. Chem. 12:567–576.Google Scholar
  36. Gobas, F.A.P.C., and Morrison, H.A. 2000. Bioconcentration and biomagnification in the aquatic environment, pp. 189–231. In R.S. Boethling and D. Mackay [eds.], Handbook of property estimation methods for chemicals: environmental and health sciences. Lewis, Boca Raton.Google Scholar
  37. Goulden, C.E., and Place, A.R. 1990. Fatty acid synthesis and accumulation rates in daphniids. J. Exp. Zool. 256:168–178.Google Scholar
  38. Graeve, M., Albers, C., and Kattner, G. 2005. Assimilation and biosynthesis of lipids in Arctic Calanus species based on feeding experiments with a 13C labelled diatom. J. Exp. Mar. Biol. Ecol. 317:109–125.Google Scholar
  39. Greenfield, B.K., Davis, J.A., Fairey, R., Roberts, C., Crane, D., and Ichikawa, G. 2005. Seasonal, interannual, and long-term variation in sport fish contamination, San Francisco Bay. Sci. Total Environ. 336:25–43.PubMedGoogle Scholar
  40. Gundersen, P., Olsvik, P.A., and Steinnes, E. 2001. Variations in heavy metal concentrations and speciation in two mining-polluted streams in central Norway. Environ. Toxicol. Chem. 20:978–984.PubMedGoogle Scholar
  41. Guschina, I.A., and Harwood, J.L. 2006. Lipids and lipid metabolism in eukaryotic algae. J. Lipid Res. 45:160–186.Google Scholar
  42. Hagen, W., and Auel, H. 2001. Seasonal adaptations and the role of lipids in oceanic zooplankton. Zool.-Anal. Comp. Syst. 104:313–326.Google Scholar
  43. Hawker, D.W.; Connell, D.W. 1988. Octanol-water partition coefficients of polychlorinated biphenyl congeners. Environ. Sci. Technol. 22:382–387.Google Scholar
  44. Hebert, C.E., and Keenleyside, K.A. 1995. To normalize or not to normalize? Fat is the question. Environ. Toxicol. Chem. 14:801–807.Google Scholar
  45. Hebert, C.E., Arts, M.T., and Weseloh, D.V.C. 2006. Ecological tracers can quantify food web structure and change. Environ. Sci. Technol. 40:5618–5623.PubMedGoogle Scholar
  46. Hop, H., Borgå, K., Gabrielsen, G.W., Kleivane, L.K., and Skaare, J.U. 2002. Food web magnification of persistent organic pollutants in poikilotherms and homeotherms from the Barents Sea. Environ. Sci. Technol. 36:2589–2597.PubMedGoogle Scholar
  47. Incardona, J.P., Day, H.L., Collier, T.K., and Scholz, N.L. 2006. Developmental toxicity of 4-ring polycyclic aromatic hydrocarbons in zebrafish is differentially dependent on AH receptor isoforms and hepatic cytochrome P4501A metabolism. Toxicol. Appl. Pharmacol. 217:308–321.PubMedGoogle Scholar
  48. Iverson, S.J., Field, C., Bowen, W.D., and Blanchard, W. 2004. Quantitative fatty acid signature analysis: a new method of estimating predator diets. Ecol. Monogr. 74:211–235.Google Scholar
  49. Johnston, T.A., Fisk, A.T., Whittle, D.M., and Muir, D.C.G. 2002. Variation in organochlorine bioaccumulation by a predatory fish; gender, geography, and data analysis methods. Environ. Sci. Technol. 36:4238–4244.PubMedGoogle Scholar
  50. Jüttner, F. 2005. Evidence that polyunsaturated aldehydes of diatoms are repellents for pelagic crustacean grazers. Aquat. Ecol. 39:271–282.Google Scholar
  51. Kainz, M., and Mazumder, A. 2005. Effect of algal and bacterial diet on methyl mercury concentrations in zooplankton. Environ. Sci. Technol. 39:1666–1672.PubMedGoogle Scholar
  52. Kainz, M., Lucotte, M., and Parrish, C.C. 2002. Methyl mercury in zooplankton – the role of size, habitat and food quality. Can. J. Fish. Aquat. Sci. 59:1606–1615.Google Scholar
  53. Kainz, M., Lucotte, M., and Parrish, C.C. 2003. Relationships between organic matter composition and methyl mercury content of offshore and carbon-rich littoral sediments in an oligotrophic lake. Can. J. Fish. Aquat. Sci. 60:888–896.Google Scholar
  54. Kainz, M., Arts, M.T., and Mazumder, A. 2004. Essential fatty acids within the planktonic food web and its ecological role for higher trophic levels. Limnol. Oceanogr. 49:1784–1793.Google Scholar
  55. Kainz, M., Telmer, K., and Mazumder, A. 2006. Bioaccumulation patterns of methyl mercury and essential fatty acids in the planktonic food web and fish. Sci. Total Environ. 368:271–282.PubMedGoogle Scholar
  56. Kainz, M., Arts, M.T., and Mazumder, A. 2008. Essential versus potentially toxic dietary substances a seasonal assessment of essential fatty acids and methyl mercury concentrations in the planktonic food web. Env. Poll.; 155:262–270.Google Scholar
  57. Kaneda, T. 1991. Iso- and anteiso-fatty acids in bacteria – biosynthesis, function, and taxonomic significance. Microbiol. Rev. 55:288–302.PubMedGoogle Scholar
  58. Kelly, B.C., Gobas, F.A.P.C., and McLachlan, M.S. 2004. Intestinal absorption and biomagnification of organic contaminants in fish, wildlife, and humans. Environ. Toxicol. Chem. 23:2324–2336.PubMedGoogle Scholar
  59. Kelly, E.N., Schindler, D.W., St. Louis, V.L., Donald, D.B., and Vlaclicka, K.E. 2006. Forest fire increases mercury accumulation by fishes via food web restructuring and increased mercury inputs. Proc. Natl. Acad. Sci. USA 103:19380–19385.PubMedGoogle Scholar
  60. Kidd, K.A., Schindler, D.W., Hesslein, R.H., Ross, B.J., Koczanski, K., Stephens, G.R., and Muir, D.C.G. 1998. Effects of trophic position and lipid on organochlorine concentrations in fishes from subarctic lakes in Yukon Territory. Can. J. Fish. Aquat. Sci. 55:869–881.Google Scholar
  61. Kidd, K.A., Bootsma, H.A., Hesslein, R.H, Muir, D.C.G, and Hecky, R.E. 2001. Biomagnification of DDT through the benthic and pelagic food webs of Lake Malawi, East Africa: Importance of trophic level and carbon source. Environ. Sci. Technol. 35:14–20.PubMedGoogle Scholar
  62. Kiron, V., Fukuda, H., Takeuchi, T., and Watanabe, T. 1995. Essential fatty acid nutrition and defense mechanisms in rainbow trout Oncorhynchus mykiss. Comp. Biochem. Physiol. A Physiol. 111:361–367.Google Scholar
  63. Klein Breteler, W.C.M., Schogt, N., Baas, M., Schouten, S., and Kraay, G.W. 1999. Trophic upgrading of food quality by protozoans enhancing copepod growth: role of essential lipids. Mar. Biol. 135:191–198.Google Scholar
  64. Konwick, B.J., A.W. Garrison, M.C. Black, J.K. Avants and A.T. Fisk. 2006. Bioaccumulation, biotransformation, and metabolite formation of fipronil and chiral legacy pesticides in rainbow trout. Environ. Sci. Technol. 40:2930–2936.PubMedGoogle Scholar
  65. Kraemer, L.D., Campbell, P.G.C., and Hare, L. 2005. Dynamics of Cd, Cu and Zn accumulation in organs and sub-cellular fractions in field transplanted juvenile yellow perch (Perca flavescens). Environ. Pollut. 138:324–337.PubMedGoogle Scholar
  66. Kwon, T.D., Fisher, S.W., Kim, G.W., Hwang, H., and Kim, J.E. 2006. Trophic transfer and biotransformation of polychlorinated biphenyls in zebra mussel, round goby, and smallmouth bass in Lake Erie, USA. Environ. Toxicol. Chem. 25:1068–1078.PubMedGoogle Scholar
  67. Mackay, D. 1982. Correlation of bioconcentration factors. Environ. Sci. Technol. 16:274–278.Google Scholar
  68. Mackay, D., and Paterson, S. 1981. Calculating fugacity. Environ. Sci. Technol. 15:1006–1013.Google Scholar
  69. Mackay, D., Shiu, W.-Y., and Ma, K.C. 2000. Physical-chemical properties and environmental fate handbook on CD. CRC Press, Boca Raton.Google Scholar
  70. Martin-Creuzburg, D., and von Elert, E. 2004. Impact of 10 dietary sterols on growth and reproduction of Daphnia galeata. J. Chem. Ecol. 30:483–500.PubMedGoogle Scholar
  71. Mason, R.P., Reinfelder, J.R., and Morel, F.M.M. 1996. Uptake, toxicity, and trophic transfer of mercury in a coastal diatom. Environ. Sci. Technol. 30:1835–1845.Google Scholar
  72. McIntyre, J.K., and Beauchamp, DA. 2007. Age and trophic position dominate bioaccumulation of mercury and organochlorines in the food web of Lake Washington. Sci. Total Environ. 372:571–584.PubMedGoogle Scholar
  73. McMeans, B.C., Borgå, K., Bechtol, W.R., Higginbotham, D., and Fisk, A.T. 2007. Essential and non-essential element concentrations in two sleeper shark species collected in arctic waters. Environ. Pollut. 148:281–290.PubMedGoogle Scholar
  74. Miralto, A., Barone, G., Romano, G., Poulet, S. A., Ianora, A., Russo, G. L., Buttino, I., Mazzarella, G., Laabir, M., Cabrinik, M., Giacobbe, M. G. 1999. The insidious effect of diatoms on copepod reproduction. Nature 402:173–176.Google Scholar
  75. Morel, F.M.M., Kraepiel, A.M.L., and Amyot, M. 1998. The chemical cycle and bioaccumulation of mercury. Ann. Rev. Ecol. Syst. 29:543–566.Google Scholar
  76. Müller-Navarra, D.C., Brett, M.T., Park, S., Chandra, S., Ballantyne, A.P., Zorita, E., Goldman, C. R. 2004. Unsaturated fatty acid content in seston and tropho-dynamic coupling in lakes. Nature 427:69–72.PubMedGoogle Scholar
  77. Müller-Navarra, D.C., Brett, M.T., Liston, A.M., and Goldman, C.R. 2000. A highly unsaturated fatty acid predicts carbon transfer between primary producers and consumers. Nature 403:74–77.PubMedGoogle Scholar
  78. Napolitano, G.E. 1999. Fatty acids as trophic and chemical markers in freshwater ecosystems, pp. 21–44. In M.T. Arts, and B.C wainman (eds.), Lipids in freshwater ecosystems. Springer, New York.Google Scholar
  79. Newman, M.C. 1998. Fundamentals of Ecotoxicology. Ann Arbor Press, Chelsea, MI, p. 402.Google Scholar
  80. Orihel, D. M., Paterson, M.J., Gilmour, C.C., Bodaly, R.A., Blanchfield, P.J., Hintelmann, H., Harris, R. C., Rudd, J. W. M. 2006. Effect of loading rate on the fate of mercury in littoral mesocosms. Environ. Sci. Technol. 40:5992–6000.PubMedGoogle Scholar
  81. Parrish, C.C, Whiticar, M., and Puvanendran, V. 2007. Is omega 6 docosapentaenoic acid an essential fatty acid during early ontogeny in marine fauna? Limnol. Oceanogr. 52:476–479.Google Scholar
  82. Paterson, G., Drouillard, K.G, and Haffner, G.D. 2006. An evaluation of stable nitrogen isotopes and polychlorinated biphenyls as bioenergetic tracers in aquatic systems. Can. J. Fish. Aquat. Sci. 63:628–641.Google Scholar
  83. Paterson, G., Drouillard, K.G., and Haffner, G.D. 2007. PCB elimination by yellow perch (Perca flavescens) during an annual temperature cycle. Environ. Sci. Technol. 41:824–829.PubMedGoogle Scholar
  84. Pereira, S.L., Leonard, A.E., Huang, Y.S., Chuang, L.T., and Mukerji, P. 2004. Identification of two novel microalgal enzymes involved in the conversion of the omega 3-fatty acid, eicosapentaenoic acid, into docosahexaenoic acid. Biochem. J. 384:357–366.PubMedGoogle Scholar
  85. Persson, J., and Vrede, T. 2006. Polyunsaturated fatty acids in zooplankton: variation due to taxonomy and trophic position. Freshw. Biol. 51:887–900.Google Scholar
  86. Pickhardt, P.C., and Fisher, N.S. 2007. Accumulation of inorganic and methylmercury by freshwater phytoplankton in two contrasting water bodies. Environ. Sci. Technol. 41:125–131.PubMedGoogle Scholar
  87. Pickhardt, P.C., Folt, C.L., Chen, C.Y., Klaue, B., and Blum, J.D. 2002. Algal blooms reduce the uptake of toxic methylmercury in freshwater food webs. Proc. Natl. Acad. Sci. USA 99:4419–4423.PubMedGoogle Scholar
  88. Rangan, V.S., and Smith, S. 2004. Fatty acid synthesis in eukaryotes, pp. 151–179. In D.E. Vance and J.E. Vance [eds.], Biochemistry of lipids, lipoporteins and membranes. Elsevier, Amsterdam.Google Scholar
  89. Rasmussen, J.B., Rowan, D.J., Lean, D.R.S., and Carey, J.H. 1990. Food chain structure in Ontario lakes determines PCB levels in lake trout (Salvelinus namaycush) and other pelagic fish. Can. J. Fish. Aquat. Sci. 47:2030–2038.Google Scholar
  90. Ravet, J.L., Brett, M.T., and Müller-Navarra, D.C. 2003. A test of the role of polyunsaturated fatty acids in phytoplankton food quality for Daphnia using liposome supplementation. Limnol. Oceanogr. 48:1938–1947.Google Scholar
  91. Rohr, J.R., and Crumrine, P.W. 2005. Effects of an herbicide and an insecticide on pond community structure and processes. Ecol. Appl. 15:1135–1147.Google Scholar
  92. Russell, R.W., Gobas, F., and Haffner, G.D. 1999. Role of chemical and ecological factors in trophic transfer of organic chemicals in aquatic food webs. Environ. Toxicol. Chem. 18:1250–1257.Google Scholar
  93. Sargent, J.R., McEvoy, L., Estevez, A., Bell, G., Bell, M., Henderson, J., Tocher, D. 1999. Lipid nutrition of marine fish during early development: current status and future directions Aquaculture. 179:217–229.Google Scholar
  94. Schwarzenbach, R.P., Gschwend, P.M., and Imboden, D.M., 2003. Environmental Organic Chemistry 2nd Edition, wiley-Interscience.Google Scholar
  95. Scott, C.L., Kwasniewski, S., Falk-Petersen, and S., Sargent, R.J. 2002. Species differences, origins and functions of fatty alcohols and fatty acids in the wax esters and phospholipids of Calanus hyperboreus, C. glacialis and C. finmarchicus from arctic waters. Mar. Ecol. Prog. Ser. 235:127–134.Google Scholar
  96. Scott, G.R., and Sloman, K.A. 2004. The effects of environmental pollutants on complex fish behaviour: integrating behavioural and physiological indicators of toxicity. Aquat. Toxicol. 68:369–392.PubMedGoogle Scholar
  97. St. Louis, V.L., Rudd, J.W.M., Kelly, C.A., Bodaly, R.A., Paterson, M.J., Beaty, K.G., Hesslein, R.H., Heyes, A., and Majewski, A.R. 2004. The rise and fall of mercury methylation in an experimental reservoir. Environ. Sci. Technol. 38:1348–1358.PubMedGoogle Scholar
  98. Sun, M.-Y., and Wakeham, S.G. 1994. Molecular evidence for degradation and preservation of organic matter in the anoxic Black Sea basin. Geochim. Cosmochim. Acta 58:3395–3406.Google Scholar
  99. Sushchik, N.N., Kalacheva, G.S., Zhila, N.O., Gladyshev, M.I., and Volova, T.G. 2003. A temperature dependence of the intra- and extracellular fatty-acid composition of green algae and cyanobacterium. Russ. J. Plant Physiol. 50:374–380.Google Scholar
  100. Swackhamer, D.L., and Skoglund, R.S. 1993. Bioaccumulation of PCBs by algae: kinetics versus equilibrium. Environ. Toxicol. Chem. 12:831–838.Google Scholar
  101. Tanabe, S. 2002. Contamination and toxic effects of persistent endocrine disrupters in marine mammals and birds. Mar. Poll. Bull. 45:69–77.Google Scholar
  102. Thomann, R.V. 1981. Equilibrium model of fate of microcontaminants in diverse aquatic food chains. Can. J. Fish. Aquat. Sci. 38:280–296.Google Scholar
  103. Thomann, R.V. 1989. Bioaccumulation model of organic-chemical distribution in aquatic food-chains. Environ. Sci. Tehcnol. 23: 699–707.Google Scholar
  104. Tocher, D.R. 2003. Metabolism and functions of lipids and fatty acids in teleost fish. Rev. Fish. Sci. 11:107–184.Google Scholar
  105. Trudel, M., and Rasmussen, J.B. 2006. Bioenergetics and mercury dynamics in fish: a modelling perspective. Can. J. Fish. Aquat. Sci. 63:1890–1902.Google Scholar
  106. van Wezel, A.P, and Opperhuizen, A. 1995. Thermodynamics of partitioning of a series of chlorobenzenes to fish storage lipids, in comparison to partitioning to phospholipids. Chemosphere 31:3605–3615.Google Scholar
  107. Viso, A.C., and Marty, J.C. 1993. Fatty acids from 28 marine microalgae. Phytochem. 34:1521–1533.Google Scholar
  108. Volkman, J.K., Barrett, S.M., Blackburn, S.I., Mansour, M.P., Sikes, E.L., and Gelin, F. 1998. Microalgal biomarkers: A review of recent research developments. Org. Geochem. 29:1163–1179.Google Scholar
  109. von Elert, E. 2002. Determination of limiting polyunsaturated fatty acids in Daphnia galeata using a new method to enrich food algae with single fatty acids. Limnol. Oceanogr. 47:1764–1773.Google Scholar
  110. Wang, W.X., and Fisher, N.S. 1998. Accumulation of trace elements in a marine copepod. Limnol. Oceanogr. 43:273–283.Google Scholar
  111. Wang, W.X., and Fisher, N.S. 1999. Assimilation efficiencies of chemical contaminants in aquatic invertebrates: A synthesis. Environ. Toxicol. Chem. 18:2034–2045.Google Scholar
  112. Wong, C.S., Mabury, S.A., Whittle, D.M., Backus, S.M., Teixeira, C., DeVault, D.S., Bronte, C.R., and Muir, D.C.G. 2004. Organochlorine compounds in Lake Superior: Chiral polychlorinated biphenyls and biotransformation in the aquatic food web. Environ. Sci. Technol. 38:84–92.PubMedGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC 2009

Authors and Affiliations

  1. 1.Biologische StationLunz am SeeAustria
  2. 2.Department of Biology (Great Lakes Institute for Environmental Research)University of WindsorWindsorCanada

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