Exposure-dose-response relationships of the freshwater bivalve Hyridella australis to cadmium spiked sediments

Aquatic Toxicology

Volumn 152, Issue , 2014, Pages 361-371

  Marasinghe Wadige, Chamani P M ^a   Maher, William A ^a   Taylor, Anne M ^a   Krikowa, Frank ^a  

^a UNIVERSITY OF CANBERRA   (Australia)

Author keywords

Biologically active cadmium; Biologically detoxified cadmium; Biomarkers; Oxidative stress; Spiked sediments; Sub cellular partitioning

Indexed keywords

CADMIUM; CALCIUM;

BIOACCUMULATION; BIOMARKER; BIOTA; BIVALVE; CADMIUM; CONCENTRATION (COMPOSITION); ENVIRONMENTAL STRESS; FRESHWATER ENVIRONMENT; LIPID; MICROCOSM; PROTEIN; SEDIMENT;

ANIMAL TISSUE; ARTICLE; BIVALVE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; DETOXIFICATION; ENVIRONMENTAL EXPOSURE; FEMALE; GILL; HEPATOPANCREAS; HYRIDELLA AUSTRALIS; LIPID PEROXIDATION; LYSOSOME; LYSOSOME MEMBRANE; MALE; MEMBRANE STABILIZATION; MICROSOME; MITOCHONDRION; NONHUMAN; OXIDATIVE STRESS; POLLUTION MONITORING; PRIORITY JOURNAL; SEDIMENT; TISSUE DISTRIBUTION; TOXICITY TESTING; WATER CONTAMINATION; WATER POLLUTION INDICATOR;

BIOLOGICALLY ACTIVE CADMIUM; BIOLOGICALLY DETOXIFIED CADMIUM; BIOMARKERS; OXIDATIVE STRESS; SPIKED SEDIMENTS; SUB-CELLULAR PARTITIONING;

ANIMALS; BIVALVIA; CADMIUM; ENVIRONMENTAL EXPOSURE; FRESH WATER; GEOLOGIC SEDIMENTS; HEPATOPANCREAS; WATER POLLUTANTS, CHEMICAL;

EID: 84900404030     PISSN: 0166445X     EISSN: 18791514     Source Type: Journal    
DOI: 10.1016/j.aquatox.2014.04.016     Document Type: Article

References (84)

1. Adams S., Shorey C., Byrne M. An ultrastructural and microanalytical study of metal-ion content in granular concretions of the freshwater mussel Hyridella depressa. Micron 1997, 28(1):1-11.
2. Amiard J.C., Geffard A., Amiard-Triquet C., Crouzet C. Relationship between the lability of sediment-bound metals (Cd, Cu, Zn) and their bioaccumulation in benthic invertebrates. Estuar. Coast. Shelf Sci. 2007, 72(3):511-521.
3. ANZECC/ARMCANZ Australian and New Zealand guidelines for fresh and marine water quality 2000, Australian and New Zealand Environment and Conservation Council/Agriculture and resource Management council of Australia and New Zealand, Canberra, ACT.
4. Arakel A.V. Towards developing sediment quality assessment guidelines for aquatic systems: an Australian perspective. Aust. J. Earth Sci. 1995, 42(4):335-369.
5. ASTM Standard guide for determination of the bioaccumulation of sediment-associated contaminants by benthic invertebrates, E1688-10 2010, American Society for Testing and Materials, West Conshohocken, PA.
6. Baldwin S., Deaker M., Maher W. Low-volume microwave digestion of marine biological tissues for the measurement of trace elements. Analyst 1994, 119(8):1701-1704.
7. Bervoets L., Voets J., Covaci A., Chu S., Qadah D., Smolders R., Schepens P., Blust R. Use of transplanted zebra mussels (Dreissena polymorpha) to assess the bioavailability of microcontaminants in Flemish surface waters. Environ. Sci. Technol. 2005, 39(6):1492-1505.
8. Besser J.M., Brumbaugh W.G., Kemble N.E., Ivey C.D., Kunz J.L., Ingersoll C.G., Rudel D. Toxicity of nickel-spiked freshwater sediments to benthic invertebrates-Spiking methodology, species sensitivity, and nickel bioavailability 2011, 5225. US Geological Survey, Scientific Investigations Report.
9. Bonneris E., Giguère A., Perceval O., Buronfosse T., Masson S., Hare L., Campbell P.G.C. Sub-cellular partitioning of metals (Cd, Cu, Zn) in the gills of a freshwater bivalve Pyganodon grandis: role of calcium concretions in metal sequestration. Aquat. Toxicol. 2005, 71(4):319-334.
10. Bonneris E., Perceval O., Masson S., Hare L., Campbell P.G.C. Sub-cellular partitioning of Cd, Cu and Zn in tissues of indigenous unionid bivalves living along a metal exposure gradient and links to metal-induced effects. Environ. Pollut. 2005, 135(2):195-208.
11. Borković-Mitić S., Pavlović S., Perendija B., Despotović S., Gavrić J., Gačić Z., Saičić Z. Influence of some metal concentrations on the activity of antioxidant enzymes and concentrations of vitamin E and SH-groups in the digestive gland and gills of the freshwater bivalve Unio tumidus from the Serbian part of Sava River. Ecol. Indic. 2013, 32:212-221.
12. Brown D., Parsons T. Relationship between cytoplasmic distribution of mercury and toxic effects to zooplankton and chum salmon (Oncorhynchus keta) exposed to mercury in a controlled ecosystem. J. Fish. Board Can. 1978, 35(6):880-884.
13. Byrne M., Vesk P.A. Elemental composition of mantle tissue granules in Hyridella depressa (Unionida) from the Hawkesbury-Nepean River system, Australia: inferences from catchment chemistry. Mar. Freshw. Res. 2000, 51(2):183-192.
14. Campbell P.G.C., Giguère A., Bonneris E., Hare L. Cadmium-handling strategies in two chronically exposed indigenous freshwater organisms-the yellow perch (Perca flavescens) and the floater mollusc (Pyganodon grandis). Aquat. Toxicol. 2005, 72(1-2):83-97.
15. Cayman Antioxidant Assay Kit User Protocol 709001 2011.
16. Chan M., Othman R., Zubir D., Salmijah S. Induction of a putative metallothionein gene in the blood cockle, Anadara granosa, exposed to cadmium. Comp. Biochem. Physiol. C: Toxicol. Pharmacol. 2002, 131(2):123-132.
17. Chelomin V.P., Zakhartsev M.V., Kurilenko A.V., Belcheva N.N. An in vitro study of the effect of reactive oxygen species on subcellular distribution of deposited cadmium in digestive gland of mussel Crenomytilus grayanus. Aquat. Toxicol. 2005, 73(2):181-189.
18. Cherkasov A.S., Biswas P.K., Ridings D.M., Ringwood A.H., Sokolova I.M. Effects of acclimation temperature and cadmium exposure on cellular energy budgets in the marine mollusk Crassostrea virginica: linking cellular and mitochondrial responses. J. Exp. Biol. 2006, 209(7):1274-1284.
19. Cooper S., Bonneris E., Michaud A., Pinel-Alloul B., Campbell P.G.C. Influence of a step-change in metal exposure (Cd, Cu, Zn) on metal accumulation and subcellular partitioning in a freshwater bivalve, Pyganodon grandis: A long-term transplantation experiment between lakes with contrasting ambient metal levels. Aquat. Toxicol. 2013, 132-133(0):73-83.
20. Cossu C., Doyotte A., Babut M., Exinger A., Vasseur P. Antioxidant biomarkers in freshwater bivalves, Unio tumidus, in response to different contamination profiles of aquatic sediments. Ecotoxicol. Environ. Saf. 2000, 45(2):106-121.
21. Cossu C., Doyotte A., Jacquin M., Babut M., Exinger A., Vasseur P. Glutathione reductase, selenium-dependent glutathione peroxidase, glutathione levels, and lipid peroxidation in freshwater bivalves, Unio tumidus, as biomarkers of aquatic contamination in field studies. Ecotoxicol. Environ. Saf. 1997, 38(2):122-131.
22. Couillard Y., Campbell P., Auclair J., Pellerin-Massicotte J. Field transplantation of a freshwater bivalve Pyganodon grandis, across a metal contamination gradient. II. Metallothionein response to Cd and Zn exposure, evidence for cytotoxicity, and links to effects at higher levels of biological organization. Can. J. Fish. Aquat. Sci. 1995, 52(4):703-715.
23. Dabas A., Nagpure N., Kumar R., Kushwaha B., Kumar P., Lakra W. Assessment of tissue-specific effect of cadmium on antioxidant defense system and lipid peroxidation in freshwater murrel, Channa punctatus. Fish Physiol. Biochem. 2012, 38(2):469-482.
24. Das P., Samantaray S., Rout G. Studies on cadmium toxicity in plants: a review. Environ. Pollut. 1997, 98(1):29-36.
25. Désy J.C., Amyot M., Pinel-Alloul B., Campbell P.G.C. Relating cadmium concentrations in three macrophyte-associated freshwater invertebrates to those in macrophytes, water and sediments. Environ. Pollut. 2002, 120(3):759-769.
26. Doyen P., Vasseur P., Rodius F. Identification, sequencing and expression of selenium-dependent glutathione peroxidase transcript in the freshwater bivalve Unio tumidus exposed to Aroclor 1254. Comp. Biochem. Physiol. C: Toxicol. Pharmacol. 2006, 144(2):122-129.
27. Duruibe J., Ogwuegbu M., Egwurugwu J. Heavy metal pollution and human biotoxic effects. Int. J. Phys. Sci. 2007, 2(5):112-118.
28. Fishbein L. Sources, transport and alterations of metal compounds: an overview. I. Arsenic, beryllium, cadmium, chromium, and nickel. Environ. Health Persp. 1981, 40:43.
29. Garmendia L., Soto M., Vicario U., Kim Y., Cajaraville M.P., Marigomez I. Application of a battery of biomarkers in mussel digestive gland to assess long-term effects of the prestige oil spill in Galicia and Bay of Biscay: tissue-level biomarkers and histopathology. J. Environ. Monit. 2011, 13(4):915-932.
30. Giambérini L., Cajaraville M.P. Lysosomal responses in the digestive gland of the freshwater mussel, Dreissena polymorpha, experimentally exposed to cadmium. Environ. Res. 2005, 98(2):210-214.
31. Giguère A., Couillard Y., Campbell P.G.C., Perceval O., Hare L., Pinel-Alloul B., Pellerin J. Steady-state distribution of metals among metallothionein and other cytosolic ligands and links to cytotoxicity in bivalves living along a polymetallic gradient. Aquat. Toxicol. 2003, 64(2):185-200.
32. Graham J.M. Homogenization of tissues and cells. Subcellular Fractionation - A Practical Approach 1997, 1-29. Oxford University Press, Oxford, England, UK. J.M. Graham, D. Rickwood (Eds.).
33. Guidi P., Frenzilli G., Benedetti M., Bernardeschi M., Falleni A., Fattorini D., Regoli F., Scarcelli V., Nigro M. Antioxidant, genotoxic and lysosomal biomarkers in the freshwater bivalve (Unio pictorum) transplanted in a metal polluted river basin. Aquat. Toxicol. 2010, 100(1):75-83.
34. Gundacker C. Comparison of heavy metal bioaccumulation in freshwater molluscs of urban river habitats in Vienna. Environ. Pollut. 2000, 110(1):61-71.
35. Hemelraad J., Holwerda D.A., Zandee D.I. Cadmium kinetics in freshwater clams. I. The pattern of cadmium accumulation in Anodonta cygnea. Arch. Environ. Contam. Toxicol. 1986, 15(1):1-7. (in English).
36. Kamunde C. Early subcellular partitioning of cadmium in gill and liver of rainbow trout (Oncorhynchus mykiss) following low-to-near-lethal waterborne cadmium exposure. Aquat. Toxicol. 2009, 91(4):291-301.
37. Landis W.G., Sofield R.M., Yu M.-H. Introduction to Environmental Toxicology: Molecular Substructures to Ecological Landscapes 2011, CRC, Boca Raton, FL. 4th ed.
38. Langston W., Zhou M. Evaluation of the significance of metal-binding proteins in the gastropod Littorina littorea. Mar. Biol. 1986, 92(4):505-515.
39. Luoma S.N., Rainbow P.S. Why is metal bioaccumulation so variable? Biodynamics as a unifying concept. Environ. Sci. Technol. 2005, 39(7):1921-1931.
40. Macklin M.G., Hudson-Edwards K.A., Dawson E.J. The significance of pollution from historic metal mining in the Pennine orefields on river sediment contaminant fluxes to the North Sea. Sci. Total Environ. 1997, 194-195:391-397.
41. Maher W., Forster S., Krikowa F., Snitch P., Chapple G., Craig P. Measurement of trace elements and phosphorus in marine animal and plant tissues by low-volume microwave digestion and ICP-MS. At. Spectrosc. (Norwalk, CT) 2001, 22(5):361-370.
42. Marasinghe Wadige C.P.M., Taylor A.M., Maher W.A., Ubrihien R.P., Krikowa F. Effects of lead-spiked sediments on freshwater bivalve, Hyridella australis: linking organism metal exposure-dose-response. Aquat. Toxicol. 2014, 149:83-93.
43. Marigomez I., Soto M., Cajaraville M.P., Angulo E., Giamberini L. Cellular and subcellular distribution of metals in molluscs. Microsc. Res. Tech. 2002, 56(5):358-392.
44. Markich S.J., Brown P.L., Jeffree R.A. Divalent metal accumulation in freshwater bivalves: an inverse relationship with metal phosphate solubility. Sci. Total Environ. 2001, 275(1-3):27-41.
45. Markich S.J., Brown P.L., Jeffree R.A., Lim R.P. The effects of pH and dissolved organic carbon on the toxicity of cadmium and copper to a freshwater bivalve: further support for the extended free ion activity model. Arch. Environ. Contam. Toxicol. 2003, 45(4):479-491.
46. Markich S.J., Jeffree R.A. Absorption of divalent trace metals as analogues of calcium by Australian freshwater bivalves: an explanation of how water hardness reduces metal toxicity. Aquat. Toxicol. 1994, 29(3):257-290.
47. Mason A., Jenkins K. Metal detoxification in aquatic organisms. Metal Speciation and Bioavailability in Aquatic Systems 1995, vol. 3:479-608.
48. Moore M.N., Allen J.I., Mcveigh A., Shaw J. Lysosomal and autophagic reactions as predictive indicators of environmental impact in aquatic animals. Autophagy 2006, 2(3):217-220.
49. Moore M.N., Icarus Allen J., Mcveigh A. Environmental prognostics: an integrated model supporting lysosomal stress responses as predictive biomarkers of animal health status. Mar. Environ. Res. 2006, 61(3):278-304.
50. Perceval O., Couillard Y., Pinel-Alloul B., Bonneris E., Campbell P.G.C. Long-term trends in accumulated metals (Cd, Cu and Zn) and metallothionein in bivalves from lakes within a smelter-impacted region. Sci. Total Environ. 2006, 369(1-3):403-418.
51. Perceval O., Pinel-Alloul B., Méthot G., Couillard Y., Giguère A., Campbell P.G.C., Hare L. Cadmium accumulation and metallothionein synthesis in freshwater bivalves (Pyganodon grandis): relative influence of the metal exposure gradient versus limnological variability. Environ. Pollut. 2002, 118(1):5-17.
52. Phillips D.J.H., Rainbow P.S. Biomonitoring of Trace Aquatic Contaminants 1994, Chapman & Hall, London.
53. Pynnönen K., Holwerda D.A., Zandee D. Occurrence of calcium concretions in various tissues of freshwater mussels, and their capacity for cadmium sequestration. Aquat. Toxicol. 1987, 10(2):101-114.
54. Qiu J.W., Xie Z.C., Wang W.X. Effects of calcium on the uptake and elimination of cadmium and zinc in Asiatic clams. Arch. Environ. Contam. Toxicol. 2005, 48(2):278-287.
55. Rainbow P.S. Trace metal concentrations in aquatic invertebrates: why and so what?. Environ. Pollut. 2002, 120(3):497-507.
56. Ravera O., Cenci R., Beone G.M., Dantas M., Lodigiani P. Trace element concentrations in freshwater mussels and macrophytes as related to those in their environment. J. Limnol. 2003, 62(1):61-70.
57. Ringwood A., Hoguet J., Keppler C., Gielazyn M., Ward B., Rourk A. Cellular Biomarkers (Lysosomal Destabilization, Glutathione & Lipid Peroxidation) in Three Common Estuarine Species: A Methods Handbook 2003, Marine Resources Research Institute, South Carolina Department of Natural Resources, Charleston.
58. Roesijadi G. Metallothioneins in metal regulation and toxicity in aquatic animals. Aquat. Toxicol. 1992, 22(2):81-113.
59. Simkiss K., Taylor M.G. Metal fluxes across the membranes of aquatic organisms. Rev. Aquat. Sci. 1989, 1(1):173-188.
60. Simpson S.L., Angel B.M., Jolley D.F. Metal equilibration in laboratory-contaminated (spiked) sediments used for the development of whole-sediment toxicity tests. Chemosphere 2004, 54(5):597-609.
61. Simpson S.L., Batley G.E. Predicting metal toxicity in sediments: a critique of current approaches. Integr. Environ. Assess. Manage. 2007, 3(1):18-31. (in English).
62. Siwela A.H., Nyathi C.B., Naik Y.S. A comparison of metal levels and antioxidant enzymes in freshwater snails, Lymnaea natalensis, exposed to sediment and water collected from Wright Dam and Lower Mguza Dam, Bulawayo, Zimbabwe. Ecotoxicol. Environ. Saf. 2010, 73(7):1728-1732.
63. Sloane P., Norris R. Relationship of AUSRIVAS-based macroinvertebrate predictive model outputs to a metal pollution gradient. J. N. Am. Benthol. Soc. 2003, 22(3):457-471.
64. Sokolova I. Cadmium effects on mitochondrial function are enhanced by elevated temperatures in a marine poikilotherm, Crassostrea virginica Gmelin (Bivalvia: Ostreidae). J. Exp. Biol. 2004, 207(15):2639-2648.
65. Sokolova I., Evans S., Hughes F. Cadmium-induced apoptosis in oyster hemocytes involves disturbance of cellular energy balance but no mitochondrial permeability transition. J. Exp. Biol. 2004, 207(19):3369-3380.
66. Sokolova I., Ringwood A., Johnson C. Tissue-specific accumulation of cadmium in subcellular compartments of eastern oysters Crassostrea virginica Gmelin (Bivalvia: Ostreidae). Aquat. Toxicol. 2005, 74(3):218-228.
67. Taylor A.M., Maher W.A. Establishing Metal Exposure-Dose-Response Relationships in Marine Organisms: Illustrated with a Case Study of Cadmium Toxicity in Tellina deltoidalis 2010, 1-57. New Oceanography Research Developments: Marine Chemistry, Ocean Floor Analyses and Marine Phytoplankton, Nova Science, NY.
68. Taylor A.M., Maher W.A. Exposure-dose-response of Anadara trapezia to metal contaminated estuarine sediments. 1. Cadmium spiked sediments. Aquat. Toxicol. 2012, 109:234-242.
69. Taylor A.M., Maher W.A. Exposure-dose-response of Anadara trapezia to metal contaminated estuarine sediments. 2. Lead spiked sediments. Aquat. Toxicol. 2012, 116-117:79-89.
70. Taylor A.M., Maher W.A. Exposure-dose-response of Tellina deltoidalis to metal-contaminated estuarine sediments: 1. Cadmium spiked sediments. Comp. Biochem. Physiol. C: Toxicol. Pharmacol. 2013, 158(1):44-55.
71. Telford K., Maher W., Krikowa F., Foster S. Measurement of total antimony and antimony species in mine contaminated soils by ICPMS and HPLC-ICPMS. J. Environ. Monit. 2008, 10(1):136-140.
72. Tessier A., Couillard Y., Campbell P., Auclair J. Modeling Cd partitioning in oxic lake sediments and Cd concentrations in the freshwater bivalve Anodonta grandis. Limnol. Oceanogr. 1993, 1-17.
73. USEPA Methods for Measuring the Toxicity and Bioaccumulation of Sediment-associated Contaminants with Freshwater Invertebrates 2000, USEPA, Duluth, MN. second edition book - 99/064 2000.
74. Valavanidis A., Vlahogianni T., Dassenakis M., Scoullos M. Molecular biomarkers of oxidative stress in aquatic organisms in relation to toxic environmental pollutants. Ecotoxicol. Environ. Saf. 2006, 64(2):178-189.
75. Van Der Oost R., Beyer J., Vermeulen N.P.E. Fish bioaccumulation and biomarkers in environmental risk assessment: a review. Environ. Toxicol. Pharmacol. 2003, 13(2):57-149.
76. Vellinger C., Parant M., Rousselle P., Immel F., Wagner P., Usseglio-Polatera P. Comparison of arsenate and cadmium toxicity in a freshwater amphipod (Gammarus pulex). Environ. Pollut. 2012, 160:66-73.
77. Viarengo A., Lowe D., Bolognesi C., Fabbri E., Koehler A. The use of biomarkers in biomonitoring: a 2-tier approach assessing the level of pollutant-induced stress syndrome in sentinel organisms. Comp. Biochem. Physiol. C: Toxicol. Pharmacol. 2007, 146(3):281-300.
78. Viarengo A., Moore M., Mancinelli G., Mazzucotelli A., Pipe R., Farrar S. Metallothioneins and lysosomes in metal toxicity and accumulation in marine mussels: the effect of cadmium in the presence and absence of phenanthrene. Mar. Biol. 1987, 94(2):251-257.
79. Wang M., Wang W.-X. Cadmium toxicity in a marine diatom as predicted by the cellular metal sensitive fraction. Environ. Sci. Technol. 2008, 42(3):940-946.
80. Wang W.-X., Rainbow P.S. Subcellular partitioning and the prediction of cadmium toxicity to aquatic organisms. Environ. Chem. 2007, 3(6):395-399.
81. Wang Y., Evans R.D. Influence of Calcium Concentrations on Cadmium Uptake by the Freshwater Mussel Ellptio complanata. Can. J. Fish. Aquat. Sci. 1993, 50(12):2591-2596.
82. Winston G.W., Di Giulio R.T. Prooxidant and antioxidant mechanisms in aquatic organisms. Aquat. Toxicol. 1991, 19(2):137-161.
83. Wright D.A., Welbourn P.M. Cadmium in the aquatic environment: a review of ecological, physiological, and toxicological effects on biota. Environ. Rev. 1994, 2(2):187-214.
84. Yap C., Hatta Y., Edward F., Tan S. Distribution of heavy metal concentrations (Cd, Cu, Ni, Fe and Zn) in the different soft tissues and shells of wild mussels Perna viridis collected from Bagan Tiang and Kuala Kedah Malaysian. Appl. Biol. 2008, 37(2):1-10.