Biogeochemical reactive-diffusive transport of heavy metals in Lake Coeur d'Alene sediments

被引:40
|
作者
Sengor, S. Sevinc [1 ]
Spycher, Nicolas F. [2 ]
Ginn, Timothy R. [1 ]
Sani, Rajesh K. [3 ]
Peyton, Brent [3 ]
机构
[1] Univ Calif Davis, Civil & Environm Engn Dept, Davis, CA 95616 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Earth Sci, Berkeley, CA 94720 USA
[3] Washington State Univ, Ctr Multiphase Environm Res, Dept Chem Engn, Pullman, WA 99164 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/j.apgeochem.2007.06.011
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Decades of runoff from precious-metal mining operations in the Lake Coeur d'Alene Basin, Idaho, have left the sediments in this lake heavily enriched with toxic metals, most notably Zn, Pb and Cu, together with As. The bioavailability, fate and transport of these metals in the sediments are governed by complex biogeochemical processes. In particular, indigenous microbes are capable of catalyzing reactions that detoxify their environments, and thus constitute an important driving component in the biogeochemical cycling of these metals. Here, the development of a quantitative model to evaluate the transport and fate of Zn, Pb and Cu in Lake Coeur d'Alene sediments is reported. The current focus is on the investigation and understanding of local-scale processes, rather than the larger-scale dynamics of sedimentation and diagenesis, with particular emphasis on metal transport through reductive dissolution of Fe hydroxides. The model includes 1-D inorganic diffusive transport coupled to a biotic reaction network including consortium biodegradation kinetics with multiple terminal electron acceptors and syntrophic consortium biotransformation dynamics of redox front. The model captures the mobilization of metals initially sorbed onto hydrous ferric oxides, through bacterial reduction of Fe(III) near the top of the sediment column, coupled with the precipitation of metal sulfides at depth due to biogenic sulfide production. Key chemical reactions involve the dissolution of ferrihydrite and precipitation of siderite and Fe sulfide. The relative rates of these reactions play an important role in the evolution of the sediment pore-water chemistry, notably pH, and directly depend on the relative activity of Fe and SO4 reducers. The model captures fairly well the observed trends of increased alkalinity, sulfide, Fe and heavy metal concentrations below the sediment-water interface, together with decreasing terminal electron acceptor concentrations with depth, including the development of anoxic conditions within about a centimeter below the lake bottom. This effort provides insights on important biogeochemical processes affecting the cycling of metals in Lake Coeur d'Alene and similar metal-impacted lacustrine environments. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2569 / 2594
页数:26
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