Ecotoxicology of metals in aquatic sediments: binding and release, bioavailability, risk assessment, and remediation

被引:238
作者
Chapman, PM
Wang, FY
Janssen, C
Persoone, G
Allen, HE
机构
[1] Evs Consultants Ltd, N Vancouver, BC V7P 2R4, Canada
[2] Univ Ghent, Lab Biol Res Aquat Pollut, B-9000 Ghent, Belgium
[3] Univ Delaware, Dept Civil & Environm Engn, Newark, DE 19716 USA
关键词
D O I
10.1139/cjfas-55-10-2221
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Major metal-binding phases in the aerobic layer of sediments are iron and manganese oxyhydroxides (FeOOH and MnOOH) and particulate organic carbon (POC). The acid-volatile sulfide (AVS) model proposed for predicting nontoxicity from metals-contaminated sediments is only applicable to anaerobic sediments. In other sediments, normalization by POC or FeOOH and MnOOH may be predictive, but binding constants are not well understood. Metal mobilization is enhanced by ligand complexation and oxidation of anaerobic sediments. Free metal ion is the most bioavailable species, but other labile metal species and nonchemical variables also determine metal bioavailability; biotic site binding models have shown promise predicting toxicity for systems of differing chemistry. Hazard identification and ecological risk assessment (ERA) depend on determining bioavailability, from water (overlying, interstitial) and food, which can be done prospectively (e.g., normalized sediment chemistry, laboratory bioassays) or retrospectively (e.g., in situ bioassays, field studies). ERA of sediment-bound metals requires primary emphasis on toxicity and consideration of the three separate transformation processes for metals in the aquatic environment, the differences between essential and nonessential metals, the complex interactions that control bioavailability, adaptation, which may occur relatively simply without appreciable cost to the organism, weight of evidence, and causality.
引用
收藏
页码:2221 / 2243
页数:23
相关论文
共 278 条
[21]   SCAVENGING RESIDENCE TIMES OF TRACE-METALS AND SURFACE-CHEMISTRY OF SINKING PARTICLES IN THE DEEP OCEAN [J].
BALISTRIERI, L ;
BREWER, PG ;
MURRAY, JW .
DEEP-SEA RESEARCH PART A-OCEANOGRAPHIC RESEARCH PAPERS, 1981, 28 (02) :101-121
[22]   EFFECTS OF STORAGE TIME ON TOXICITY OF SEDIMENTS FROM PUGET-SOUND, WASHINGTON [J].
BECKER, DS ;
GINN, TC .
ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY, 1995, 14 (05) :829-835
[23]   INSITU COLLECTION OF DIAGENETIC IRON AND MANGANESE OXYHYDROXIDES FROM NATURAL SEDIMENTS [J].
BELZILE, N ;
DEVITRE, RR ;
TESSIER, A .
NATURE, 1989, 340 (6232) :376-377
[24]  
Benson W.H., 1992, P241
[25]   Predicting the toxicity of metal-spiked laboratory sediments using acid-volatile sulfide and interstitial water normalizations [J].
Berry, WJ ;
Hansen, DJ ;
Mahony, JD ;
Robson, DL ;
DiToro, DM ;
Shipley, BP ;
Rogers, B ;
Corbin, JM ;
Boothman, WS .
ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY, 1996, 15 (12) :2067-2079
[26]  
Besser JM, 1996, ENVIRON TOXICOL CHEM, V15, P286, DOI [10.1002/etc.5620150310, 10.1897/1551-5028(1996)015&lt
[27]  
0286:EOSATV&gt
[28]  
2.3.CO
[29]  
2]
[30]   Assessment of sediment quality in dredged and undredged areas of the Trenton Channel of the Detroit River, Michigan USA, using the sediment quality triad [J].
Besser, JM ;
Giesy, JP ;
Kubitz, JA ;
Verbrugge, DA ;
Coon, TG ;
Braselton, WE .
JOURNAL OF GREAT LAKES RESEARCH, 1996, 22 (03) :683-696