Advances in environmental research

  • 제1권1호
  • /
  • Pages.15-35
  • /
  • 2012
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  • 2234-1722(pISSN)
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  • 2234-1730(eISSN)
테크노프레스 (Techno-Press)
권호 표지
DOI QR코드

DOI QR Code

Biodynamic understanding of mercury accumulation in marine and freshwater fish

  • Wang, Wen-Xiong (Division of Life Science, The Hong Kong University of Science and Technology (HKUST))
  • 투고 : 2012.02.20
  • 심사 : 2012.03.19
  • 발행 : 2012.03.25
⟨ 이전 논문 다음 논문 ⟩

초록

Mercury (Hg) is a global environmental pollutant that has been the cause of many public concerns. One particular concern about Hg in aquatic systems is its trophic transfer and biomagnification in food chains. For example, the Hg concentration increases with the increase of food chain level. Fish at the top of food chain can accumulate high concentrations of Hg (especially the toxic form, methylmercury, MeHg), which is then transferred to humans through seafood consumption. Various biological and physiochemical conditions can significantly affect the bioaccumulation of Hg-including both its inorganic (Hg(II)) and organic (MeHg) forms-in fish. There have been numerous measurements of Hg concentrations in marine and freshwater fish worldwide. Many of these studies have attempted to identify the processes leading to variations of Hg concentrations in fish species from different habitats. The development of a biokinetic model over the past decade has helped improve our understanding of the mechanisms underlying the bioaccumulation processes of Hg in aquatic animals. In this review, I will discuss how the biokinetic modeling approach can be used to reveal the interesting biodynamics of Hg in fish, such as the trophic transfer and exposure route of Hg(II) and MeHg, as well as growth enrichment (the increases in Hg concentration with fish size) and biomass dilution (the decreases in Hg concentration with increasing phytoplankton biomass). I will also discuss the relevance of studying the subcellular fates of Hg to predict the Hg bioaccessibility and detoxification in fish. Future challenges will be to understand the inter- and intra-species differences in Hg accumulation and the management/mitigation of Hg pollution in both marine and freshwater fish based on our knowledge of Hg biodynamics.

키워드

참고문헌

  1. Amlund, H., Lundebye, A.K. and Berntssen, M.H.G. (2007), "Accumulation and elimination of methylmercury in Atlantic cod (Gadus morhua L.) following dietary exposure", Aquat. Toxicol., 83(4), 323-330. https://doi.org/10.1016/j.aquatox.2007.05.008
  2. Barghigiani, C., Pellegrini, D. and Carpene, E. (1989), "Mercury binding-proteins in liver and muscle of flat fish from the northern Tyrrhenia Sea", Comp. Biochem. Phys. C, 94(1), 309-312. https://doi.org/10.1016/0742-8413(89)90184-9
  3. Bebianno, M.J., Santos, C., Canario, J., Gouveia, N., Sena-Carvalho, D. and Vale, C. (2007), "Hg and metallothionein-like proteins in the black scabbardfish Aphanopus carbo", Food Chem. Toxicol., 45(8), 1443-1452. https://doi.org/10.1016/j.fct.2007.02.003
  4. Bloom, N.S. (1992), "On the chemical form of mercury in edible fish and marine invertebrate tissue", Can. J. Fish. Aquat. Sci., 49(5), 1010-1017. https://doi.org/10.1139/f92-113
  5. Bridges, C.C. and Zalups, R.K. (2005), "Molecular and ionic mimicry and the transport of toxic metals", Toxicol. Appl. Pharm., 204(3), 274-308. https://doi.org/10.1016/j.taap.2004.09.007
  6. Chan, J., Huang, Z., Merrifield, M., Salgado, M. and Stillman, M. (2002), "Studies of metal binding reactions in metallothioneins by spectroscopic, molecular biology, and molecular modeling techniques", Coordin. Chem. Rev. 233/234, 319-339. https://doi.org/10.1016/S0010-8545(02)00176-5
  7. Chen, C.Y., Stemberger, R.S., Kamman, N.C., Mayes, B.M. and Folt, C.L. (2005), "Patterns of Hg bioaccumulation and transfer in aquatic food webs across multi-lake studies in the northeast US", Ecotoxicology, 14(1-2), 135-147. https://doi.org/10.1007/s10646-004-6265-y
  8. Chen, C.Y. and Flot, C.L. (2005), "High plankton densities reduce mercury biomagnifications", Environ. Sci. Technol., 39(1), 115-121. https://doi.org/10.1021/es0403007
  9. Choi, M.H., Cech, J.J. and Lagunas-Solar, M.C. (1998), "Bioavailability of methylmercury to sacramento blackfish (Orthodon microlepidotus): Dissolved organic carbon effects", Environ. Toxicol. Chem., 17(4), 695-701. https://doi.org/10.1002/etc.5620170425
  10. Clarkson, T.W. (1997), "The toxicology of mercury", Crit. Rev. Cl. Lab. Sci., 34(3), 369-403. https://doi.org/10.3109/10408369708998098
  11. Dang, F. and Wang, W.X. (2010), "Subcellular controls of mercury trophic transfer to a marine fish", Aquat. Toxicol., 99(4), 500-506. https://doi.org/10.1016/j.aquatox.2010.06.010
  12. Dang, F. and Wang, W.X. (2011), "Antagonistic interaction of mercury and selenium in a marine fish is dependent on their chemical species", Environ. Sci. Technol., 45(7), 3116-3122. https://doi.org/10.1021/es103705a
  13. Dang, F. and Wang, W.X. (2012), "Why mercury concentration increases with fish size? Biokinetic explanation", Environ. Pollut., 163, 192-198. https://doi.org/10.1016/j.envpol.2011.12.026
  14. Dutton, J. and Fisher, N.S. (2010), "Intraspecific comparisons of metal bioaccumulation in the uvenile Atlantic silverside Menidia mendidia", Aquat. Biol., 10(3), 211-226. https://doi.org/10.3354/ab00276
  15. Eagles-Smith, C.A., Suchanek, T.H., Colwell, A.E. and Anderson, N.L. (2008), "Mercury trophic transfer in a eutrophic lake: the importance of habitat-specific foraging", Ecol. Appl., 18(8), A196-212. https://doi.org/10.1890/06-1476.1
  16. Fitzgerald, W.F., Lamborg, C.H. and Hammerschmidt, C.R. (2007), "Marine biogeochemical cycling of mercury", Chem. Rev., 107, 641-662. https://doi.org/10.1021/cr050353m
  17. Gewurtz, S.B., Bhavsar, S.P. and Fletcher, R. (2011), "Influence of fish size and sex on mercury/PCB concentration: Importance for fish consumption advisories", Environ. Int., 37(2), 425-434. https://doi.org/10.1016/j.envint.2010.11.005
  18. Gilmour, C.C. and Riedel, G.A. (2000), "A survey of size-specific mercury concentrations in game fish from Maryland fresh and estuarine waters", Arch. Environ. Con. Tox., 39(1), 53-59. https://doi.org/10.1007/s002440010079
  19. Glover, J.B., Domino, M.E., Altman, K.C., Dillman, J.W., Castleberry, W.S., Eidson, J.P. and Mattocks, M. (2010), "Mercury in South Carolina Fishes, USA", Ecotoxicology, 19(4), 781-795. https://doi.org/10.1007/s10646-009-0455-6
  20. Gorski, P.R., Armstrong, D.E., Hurley, J.P. and Shafer, M.M. (2006), "Speciation of aqueous methylmercury influences uptake by a freshwater alga (Selenastrum capricornutum)", Environ. Toxicol. Chem., 25(2), 534-540. https://doi.org/10.1897/04-530R.1
  21. Goto, D. and Wallace, W.G. (2009), "Influences of prey- and predator-dependent processes on cadmium and methylmercury trophic transfer to mummichogs (Fundulus heteroclitus)", Can. J. Fish. Aquat. Sci., 66(5), 836-846. https://doi.org/10.1139/F09-038
  22. Greenfield, B.K., Hrabik, T.R., Harvey, C.J. and Carpenter, S.R. (2001), "Predicting mercury levels in yellow perch: use of water chemistry, trophic ecology, and spatial traits", Can. J. Fish. Aquat. Sci., 58(7), 1419-1429. https://doi.org/10.1139/f01-088
  23. Haitzer, M., Aiken, G.R. and Ryan, J.N. (2002), "Binding of mercury(II) to dissolved organic matter: the role of the mercury-to-DOM concentration ratio", Environ. Sci. Technol., 36(16), 3564-3570. https://doi.org/10.1021/es025699i
  24. Hall, B.D., Bodaly, R.A., Fudge, R.J.P., Rudd, J.W.M. and Rosenberg, D.M. (1997), "Food as the dominant pathway of methylmercury uptake by fish", Water Air Soil Poll., 100(1-2), 13-24.
  25. Harris, H.H., Pickering, I.J. and George, G.N. (2003), "The chemical form of mercury in fish", Science, 301(5637), 1203. https://doi.org/10.1126/science.1085941
  26. He, M. and Wang, W.X. (2011), "Factors affecting the bioaccessibility of methylmercury in several marine fish species", J. Agr. Food Chem., 59(13), 7155-7162. https://doi.org/10.1021/jf201424g
  27. Hill, W.R. and Larsen, I.L. (2005), "Growth dilution of metals in microalgal biofilms", Environ. Sci. Technol., 39(6), 1513-1518. https://doi.org/10.1021/es049587y
  28. Joiris, C.R., Das, H.K. and Holsbeek, L. (2000), "Mercury accumulation and speciation in marine fish from Bangladesh", Mar. Pollut. Bull., 40(5), 454-457. https://doi.org/10.1016/S0025-326X(00)00013-8
  29. Karimi, R., Chen, C.Y., Pickhardt, P.C., Fisher, N.S. and Folt, C.L. (2007), "Stoichiometric controls of mercury dilution by growth", Proceedings of the National Academy of Sciences of the United States of America, 104(18), 7477-7482. https://doi.org/10.1073/pnas.0611261104
  30. Karimi, R., Fisher, N.S. and Folt, C.L. (2010), "Multielement stoichiometry in aquatic invertebrates: when growth dilution matters", Am. Nat, 176(16), 699-709. https://doi.org/10.1086/657046
  31. Klinck, J., Dunbar, M., Brown, S., Nichols, J., Winter, A., Hughes, C. and Playle, R.C. (2005), "Influence of water chemistry and natural organic matter on active and passive uptake of inorganic mercury by gills of rainbow trout (Oncorhynchus mykiss)", Aquat. Toxicol., 72(1-2), 161-175. https://doi.org/10.1016/j.aquatox.2004.11.013
  32. Kuwabara, J.S., Arai, Y., Topping, B.R., Pickering, I.J. and George, G.N. (2007), "Mercury speciation in piscivorous fish from mining-impacted reservoirs", Environ. Sci. Technol., 41(8), 2745-2749. https://doi.org/10.1021/es0628856
  33. Lamborg, C.H., Fitzgerald, W.F., Skoog, A. and Visscher, P.T. (2004), "The abundance and source of mercury-binding organic ligands in Long Island Sound", Mar. Chem., 90(1-4), 151-163. https://doi.org/10.1016/j.marchem.2004.03.014
  34. Laporte, J.M., Truchot, J.P., Ribeyre, F. and Boudou, A. (1997), "Combined effects of water pH and salinity on the bioaccumulation of inorganic mercury and methylmercury in the shore crab Carcinus maenas", Mar. Pollut. Bull., 34(11), 880-893. https://doi.org/10.1016/S0025-326X(97)00059-3
  35. Laporte, J.M., Andres, S. and Mason, R.P. (2002), "Effect of ligands and other metals on the uptake of mercury and methylmercury across the gills and the intestine of the blue crab (Callinectes sapidus)", Comp. Biochem. Phys. C., 131(2), 185-196. https://doi.org/10.1016/S1096-4959(01)00493-6
  36. Lavigne, M., Lucotte, M. and Paquet, S. (2010), "Relationship between mercury concentration and growth rates for walleyes, Northern Pike, and Lake Trout from Quebec Lakes", N. Am. J. Fish. Manage., 30(5), 1221-1237. https://doi.org/10.1577/M08-065.1
  37. Lawson, N.M. and Mason, R.P. (1998), "Accumulation of mercury in estuarine food chains", Biogeochemistry, 40(2-3), 235-247. https://doi.org/10.1023/A:1005959211768
  38. Leaner, J.J. and Mason, R.P. (2002), "Methylmercury accumulation and fluxes across the intestine of channel catfish, Ictalurus punctatus", Comp. Biochem. Phys. C, 132(2), 247-259.
  39. Lemes, M. and Wang, F.Y. (2009), "Methylmercury speciation in fish muscle by HPLC-ICP-MS following enzymatic hydrolysis", J. Anal. Atom. Spectrom., 24, 663-668. https://doi.org/10.1039/b819957b
  40. Levinton, J.S. and Pochron, S.T. (2008), "Temporal and geographic trends in mercury concentrations in muscle tissue in five species of fish from Hudson River, USA", Environ. Toxicol. Chem., 27(8), 1691-1697. https://doi.org/10.1897/07-438.1
  41. Liu, B., Yan, H.Y., Wang, C.P., Li, Q.H., Guedron, S., Spangenberg, J.E., Feng, X.B. and Dominik, J. (2012), "Insights into low fish mercury bioaccumulation in a mercury-contaminated reservoir, Guizhou, China", Environ. Pollut., 160, 109-117. https://doi.org/10.1016/j.envpol.2011.09.023
  42. Luoma, S.N. and Rainbow, P.S. (2005), "Why is metal bioaccumulation so variable? Biodynamics as a unifying concept", Environ. Sci. Technol., 39(7), 1921-1931. https://doi.org/10.1021/es048947e
  43. Magalhaes, M.C., Costa, V., Menezes, G.M., Pinho, M.R., Santos, R.S. and Monteiro, L.R. (2007), "Intra- and inter-specific variability in total and methylmercury bioaccumulation by eight marine fish species from the Azores", Mar. Pollut. Bull., 54(10), 1654-1662. https://doi.org/10.1016/j.marpolbul.2007.07.006
  44. Mason, R.P., Reinfelder, J.R. and Morel, F.M. (1996), "Uptake, toxicity, and trophic transfer of mercury in a coastal diatom", Environ. Sci. Technol., 30(6), 1835-1845. https://doi.org/10.1021/es950373d
  45. Mathews, T. and Fisher, N.S. (2008), "Evaluating the trophic transfer of cadmium, polonium, and methylmercury in an estuarine food chain", Environ. Toxicol. Chem., 27(5), 1093-1101. https://doi.org/10.1897/07-318.1
  46. Miao, A.J. and Wang, W.X. (2004), "Relationships between cell specific growth rate and uptake rate of cadmium and zinc by a coastal diatom", Mar. Ecol-Prog. Ser., 275, 103-113. https://doi.org/10.3354/meps275103
  47. Monteiro, L.R. and Lopes, H.D. (1990), "Mercury content of swordfish, Xiphias gladius, in relation to length, weight, age, and sex", Mar. Pollut. Bull., 21(6), 293-296. https://doi.org/10.1016/0025-326X(90)90593-W
  48. 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. https://doi.org/10.1146/annurev.ecolsys.29.1.543
  49. Ni, I.H., Wang, W.X. and Tam, Y.K. (2000), "The transfer of Cd, Cr, and Zn from zooplankton to mudskipper and glassy fishes", Mar. Ecol-Prog. Ser., 194, 203-210. https://doi.org/10.3354/meps194203
  50. Nordberg, M. (1998), "Metallothioneins: historical review and state of knowledge", Talanta, 46(2), 243-254. https://doi.org/10.1016/S0039-9140(97)00345-7
  51. Onsanit, S. and Wang, W.X. (2011), "Sequestration of total and methyl mercury in different subcellular pools in marine caged fish", J. Hazard. Mater., 198, 113-122. https://doi.org/10.1016/j.jhazmat.2011.10.020
  52. Peterson, S.A. and Sickle, J.V. (2007), "Mercury concentration in fish from streams and rivers throughout the western United States", Environ. Sci. Technol., 41(1), 58-65. https://doi.org/10.1021/es061070u
  53. 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(1), 125-131. https://doi.org/10.1021/es060966w
  54. 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", Proceedings of the National Academy of Science of the United States of America, 99(7), 4419-4423. https://doi.org/10.1073/pnas.072531099
  55. Pickhardt, P.C., Stepanova, M. and Fisher, N.S. (2006), "Contrasting uptake routes and tissue distributions of inorganic and methylmercury in mosquitofish (Gambusia affinis) and redear sunfish (Lepomis microlophus)", Environ. Toxicol. Chem., 25(8), 2132-2142. https://doi.org/10.1897/05-595R.1
  56. Qiu, Y.W., Lin, D., Liu, J.Q. and Zeng, E.Y. (2011), "Bioaccumulation of trace metals in farmed fish from South China and potential risk assessment", Ecotox. Environ. Safe., 74(3), 284-293. https://doi.org/10.1016/j.ecoenv.2010.10.008
  57. Rainbow, P.S., Luoma, S.N. and Wang, W.X. (2011), "Trophically available metal - a variable feast", Environ. Pollut., 159(10), 2347-2345. https://doi.org/10.1016/j.envpol.2011.06.040
  58. Reinfelder, J.R. and Fisher, N.S. (1991), "The assimilation of elements ingested by marine copepods", Science, 251(4995), 794-796. https://doi.org/10.1126/science.251.4995.794
  59. Rypel, A.L., Arrington, D.A. and Findlay, R.H. (2008), "Mercury in southeastern US riverine fish populations linked to water body type", Environ. Sci. Technol., 42(14), 5118-5124. https://doi.org/10.1021/es8001772
  60. Simoneau, M., Lucotte, M., Garceau, S. and Laliberte, D. (2005), "Fish growth rates modulate mercury concentrations in walleye (Sander vitreus) from eastern Canadian lakes", Environ. Res., 98(1), 72-82.
  61. Sonesten, L. (2003), "Fish mercury levels in lakes-adjusting for Hg and fish-size covariation", Environ. Pollut., 125(2), 255-265. https://doi.org/10.1016/S0269-7491(03)00051-4
  62. Staudinger, M.D. (2011), "Species-and size-specific variability of mercury concentrations in four commercially important finfish and their prey from the northwest Atlantic", Mar. Pollut. Bull., 62(4), 732-740.
  63. Storelli, M.M., Barone, G., Piscitelli, G. and Marcotrigiano, G.O. (2007), "Mercury in fish: concentration vs. fish size and estimates of mercury intake", Food Addit. Contam., 24(12), 1353-1357. https://doi.org/10.1080/02652030701387197
  64. Torres-Escribano, S., Velez, D. and Montoro, R. (2010), "Mercury and methylmercury bioaccessibility in swordfish", Food Addit. Contam., 27(3), 327-337. https://doi.org/10.1080/19440040903365272
  65. Trudel, M. and Rasmussen, J. B. (2006), "Bioenergetics and mercury dynamics in fish: A modeling perspective", Can. J. Fish. Aquat. Sci., 63(8), 1890-1902. https://doi.org/10.1139/f06-081
  66. Tsui, M.T.K. and Wang, W.X. (2004), "Uptake and elimination routes of inorganic mercury and methylmercury in Daphnia magna", Environ. Sci. Technol., 38(3), 808-816. https://doi.org/10.1021/es034638x
  67. Verdouw, J.J., Macleod, C.K., Nowak, B.F. and Lyle, J.M. (2011), "Implications of age, size and region on mercury contamination in estuarine fish species", Water Air Soil Poll., 214(1-4), 297-306. https://doi.org/10.1007/s11270-010-0424-y
  68. Vieira, C., Morais, S., Ramos, S., Delerue-Matos, C. and Oliveira, M.B.P.P. (2011), "Mercury, cadmium, lead and arsenic levels in three pelagic fish species from the Atlantic Ocean: Intra- and inter-specific variability and human health risks for consumption", Food Chem. Toxicol., 49(4), 923-932. https://doi.org/10.1016/j.fct.2010.12.016
  69. Wallace, W.G. and Luoma, S.N. (2003), "Subcellular compartmentalization of Cd and Zn in two bivalves. II. The significance of trophically available metal (TAM)", Mar. Ecol-Prog. Ser., 257, 125-137. https://doi.org/10.3354/meps257125
  70. Wallace, W.G., Lee, B.G. and Luoma, S.N. (2003), "Subcellular compartmentalization of Cd and Zn in two bivalves. I. Significance of metal-sensitive fraction (MSF) and biologically detoxified metal (BDM)", Mar. Ecol-Prog. Ser., 249, 183-197. https://doi.org/10.3354/meps249183
  71. Wang, R. and Wang, W.X. (2010), "Importance of speciation in understanding mercury bioaccumulation in tilapia controlled by salinity and dissolved organic matter", Environ. Sci. Technol., 44(20), 7964-7969. https://doi.org/10.1021/es1011274
  72. Wang, R. and Wang, W.X. (2012), "Contrasting mercury accumulation patterns in tilapia (Oreochromis niloticus) and implications on somatic growth dilution", Aquat. Toxicol., 114/115, 23-30. https://doi.org/10.1016/j.aquatox.2012.02.014
  73. Wang, R., Wong, M.H. and Wang, W.X. (2011), "Coupling of methylmercury uptake with respiration and water pumping in freshwater tilapia Orechromis niloticus", Environ. Toxicol. Chem., 30(9), 2142-2147. https://doi.org/10.1002/etc.604
  74. Wang, R., Wong, M.H. and Wang, W.X. (2010), "Mercury exposure in the freshwater tilapia Orechromis niloticus", Environ. Pollut., 158(8), 2694-2701. https://doi.org/10.1016/j.envpol.2010.04.019
  75. Wang, W.X. (2002), "Interactions of trace metals and different marine food chains", Mar. Ecol-Prog. Ser., 243, 295-309. https://doi.org/10.3354/meps243295
  76. Wang, W.X. and Fisher, N.S. (1996), "Assimilation of trace elements and carbon by the mussel Mytilus edulis: Effects of food composition", Limnol. Oceanogr., 41(2), 197-207. https://doi.org/10.4319/lo.1996.41.2.0197
  77. Wang, W.X. and Fisher, N.S. (1999), "Delineating metal accumulation pathways for aquatic invertebrates", Sci. Total Environ., 237/238, 459-472. https://doi.org/10.1016/S0048-9697(99)00158-8
  78. Wang, W.X. and Rainbow, P.S. (2006), "Subcellular partitioning and the prediction of Cd toxicity to aquatic organisms", Environ. Chem., 3(6), 395-399.
  79. Wang, W.X. and Rainbow, P.S. (2008), "Comparative approach to understand metal accumulation in aquatic systems", Comp. Biochem. Physiol. C, 148(4), 315-323.
  80. Wang, W.X. and Wong, R.S.K. (2003), "Bioaccumulation kinetics and exposure pathways of inorganic mercury and methylmercury in a marine fish, the sweetlips Plectorhinchus gibbosus", Mar. Ecol-Prog. Ser., 261, 257-268. https://doi.org/10.3354/meps261257
  81. Wang, W.X., Dei, R.C.H. and Hong, H. (2005), "Seasonal study on the Cd, Se, and Zn uptake by natural coastal phytoplankton assemblage", Environ. Toxicol. Chem., 24(1), 161-169. https://doi.org/10.1897/04-125R.1
  82. Ward, D.M., Nislow, K.H., Chen, C.Y. and Folt, C.L. (2010a), "Reduced trace element concentrations in fastgrowing juvenile Atlantic salmon in natural streams", Environ. Sci. Technol., 44(9), 3245-3251. https://doi.org/10.1021/es902639a
  83. Ward, D.M., Nislow, K.H., Chen, C.Y. and Folt, C.L. (2010b), "Rapid, efficient growth reduces mercury concentrations in stream-dwelling atlantic salmon", T. Am. Fish. Soc., 139(1), 1-10. https://doi.org/10.1577/T09-032.1
  84. Watras, C.J., Back, R.C., Halvorsen, S., Hudson, R.J.M., Morrison, K.A. and Wente, S.P. (1998), "Bioaccumulation of mercury in pelagic freshwater food webs", Sci. Total. Environ., 219(2-3), 183-208. https://doi.org/10.1016/S0048-9697(98)00228-9
  85. Wiener, J.G., Martini, R.E., Sheffy, T.B. and Glass, G.E. (1990), "Factors influencing mercury concentrations in walleyes in northern Wisconsin Lakes", T. Am. Fish. Soc., 119(5), 862-870. https://doi.org/10.1577/1548-8659(1990)119<0862:FIMCIW>2.3.CO;2
  86. Xu, Y. and Wang, W.X. (2002), "Exposure and food chain transfer factor of Cd, Se, and Zn in a marine fish, Lutjanus argentimaculatus", Mar. Ecol-Prog. Ser., 238, 173-186. https://doi.org/10.3354/meps238173
  87. Zhang, L. and Wang, W.X. (2006), "Significance of subcellular metal distribution in prey in influencing the trophic transfer of metals in a marine fish", Limnol. Oceanogr., 51(5), 2008-2017. https://doi.org/10.4319/lo.2006.51.5.2008
  88. Zhang, M.Q., Zhu, Y.C. and Deng, R.W. (2002), "Evaluation of mercury emissions to the atmosphere from coal combustion, China", Ambio, 31(6), 482-484. https://doi.org/10.1579/0044-7447-31.6.482
  89. Zhong, H. and Wang, W.X. (2009), "Controls of dissolved organic matter and chloride on mercury uptake by a marine diatom", Environ. Sci. Technol., 43(23), 8998-9003. https://doi.org/10.1021/es901646k

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  3. Effects of Environmental Temperature Change on Mercury Absorption in Aquatic Organisms with Respect to Climate Warming vol.77, pp.22-24, 2014, https://doi.org/10.1080/15287394.2014.955892
  4. Mercury bioaccumulation in cartilaginous fishes from Southern New England coastal waters: Contamination from a trophic ecology and human health perspective vol.99, 2014, https://doi.org/10.1016/j.marenvres.2014.05.009
  5. In Vivo Mercury Demethylation in a Marine Fish (Acanthopagrus schlegeli) vol.51, pp.11, 2017, https://doi.org/10.1021/acs.est.7b00923
  6. Mercury in fishes from Augusta Bay (southern Italy): Risk assessment and health implication vol.56, 2013, https://doi.org/10.1016/j.fct.2013.02.025
  7. Co-selection of Mercury and Multiple Antibiotic Resistances in Bacteria Exposed to Mercury in the Fundulus heteroclitus Gut Microbiome vol.73, pp.6, 2016, https://doi.org/10.1007/s00284-016-1133-6
  8. Mercury and selenium in the food web of Lake Nahuel Huapi, Patagonia, Argentina vol.166, 2017, https://doi.org/10.1016/j.chemosphere.2016.09.085
  9. Assessing the influence of migration barriers and feeding ecology on total mercury concentrations in Dolly Varden ( Salvelinus malma ) from a glaciated and non-glaciated stream vol.580, 2017, https://doi.org/10.1016/j.scitotenv.2016.12.017
  10. Comparison of trace metals in different fish tissues of Scomberomorus spp . (“sierra”) and Lutjanus synagris (“arrayado”) from Jobos Bay and La Parguera coastal areas in Southern Puerto Rico vol.13, 2017, https://doi.org/10.1016/j.rsma.2017.03.006
  11. Selenium induces the demethylation of mercury in marine fish vol.231, 2017, https://doi.org/10.1016/j.envpol.2017.09.014
  12. Total mercury content, weight and length relationship in swordfish (Xiphias gladius) in Sri Lanka vol.6, pp.4, 2013, https://doi.org/10.1080/19393210.2013.807521
  13. Development and Validation of a Biodynamic Model for Mechanistically Predicting Metal Accumulation in Fish-Parasite Systems vol.11, pp.8, 2016, https://doi.org/10.1371/journal.pone.0161091
  14. Toxic heavy metals in human blood in relation to certain food and environmental samples in Kerala, South India 2018, https://doi.org/10.1007/s11356-017-1112-x
  15. Assessing correlations between monomethylmercury accumulation in fish and trophic states of artificial temperate reservoirs vol.580, 2017, https://doi.org/10.1016/j.scitotenv.2016.12.039
  16. Species- and habitat-specific bioaccumulation of total mercury and methylmercury in the food web of a deep oligotrophic lake vol.612, 2018, https://doi.org/10.1016/j.scitotenv.2017.08.260
  17. Organ-specific accumulation, transportation, and elimination of methylmercury and inorganic mercury in a low Hg accumulating fish vol.35, pp.8, 2016, https://doi.org/10.1002/etc.3363
  18. Influence of volcanic activity and anthropic impact in the trace element contents of fishes from the North Patagonia in a global context vol.187, pp.11, 2015, https://doi.org/10.1007/s10661-015-4910-y
  19. Kinetics of Mercury Accumulation and Elimination in Edible Glass Eel (Anguilla anguilla) and Potential Health Public Risks vol.226, pp.5, 2015, https://doi.org/10.1007/s11270-015-2431-5
  20. Natural Hg isotopic composition of different Hg compounds in mammal tissues as a proxy for in vivo breakdown of toxic methylmercury vol.8, pp.2, 2016, https://doi.org/10.1039/C5MT00286A
  21. Mercury in Wild Fish from High-Altitude Aquatic Ecosystems in the Tibetan Plateau vol.48, pp.9, 2014, https://doi.org/10.1021/es404275v
  22. In Vivo Mercury Methylation and Demethylation in Freshwater Tilapia Quantified by Mercury Stable Isotopes vol.47, pp.14, 2013, https://doi.org/10.1021/es3043774
  23. Assessing exposure risks for freshwater tilapia species posed by mercury and methylmercury vol.25, pp.6, 2012, https://doi.org/10.1007/s10646-016-1672-4
  24. Sub-ppt level voltammetric sensor for Hg2+ detection based on nafion stabilized l-cysteine-capped Au@Ag core-shell nanoparticles vol.23, pp.7, 2012, https://doi.org/10.1007/s10008-019-04298-2
  25. Understanding Food Web Mercury Accumulation Through Trophic Transfer and Carbon Processing along a River Affected by Recent Run-of-river Dams vol.55, pp.5, 2012, https://doi.org/10.1021/acs.est.0c07015
  26. An upwelling area as a hot spot for mercury biomonitoring in a climate change scenario: A case study with large demersal fishes from Southeast Atlantic (SE-Brazil) vol.269, pp.None, 2021, https://doi.org/10.1016/j.chemosphere.2020.128718
  27. Environmental and biological factors are joint drivers of mercury biomagnification in subarctic lake food webs along a climate and productivity gradient vol.779, pp.None, 2012, https://doi.org/10.1016/j.scitotenv.2021.146261
  28. Total mercury concentrations in invasive lionfish (Pterois volitans/miles) from the Atlantic coast of Florida vol.16, pp.9, 2012, https://doi.org/10.1371/journal.pone.0234534
  29. Trophic transfer and dietary exposure risk of mercury in aquatic organisms from urbanized coastal ecosystems vol.281, pp.None, 2012, https://doi.org/10.1016/j.chemosphere.2021.130836
  30. The alteration of gut microbiome community play an important role in mercury biotransformation in largemouth bass vol.204, pp.no.pa, 2012, https://doi.org/10.1016/j.envres.2021.112026