The transport and fate of Fe, Mn, Cu, Zn, Cd, Ph and SO4 in a groundwater plume and in downstream surface waters in the Coeur d'Alene Mining District, Idaho, USA

被引:38
作者
Paulson, AJ [1 ]
机构
[1] DREXEL UNIV,SCH ENVIRONM SCI ENGN & POLICY,PHILADELPHIA,PA 19104
关键词
D O I
10.1016/S0883-2927(97)00013-9
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
The controls on metal concentrations in a plume of acidic (pH 3.29-5.55) groundwater in the Moon Creek watershed in Idaho, U.S.A., were investigated with the use of property-property plots. A plot of Ca vs S demonstrated that a plume of contaminated groundwater was being diluted by infiltration of rain and creek water at shallow depths and by ambient groundwater near bedrock. The small amount of dissolved Fe (2.1 mg/l) was removed while dissolved Pb was added, reaching a maximum concentration of 0.37 mg/l. The other metals (Zn less than or equal to 16, Al less than or equal to 6.2, Cu less than or equal to 2.1 and Cd less than or equal to 0.077 mg/l) in the shallow groundwater were essentially conserved until they emerged as a seep along the creek bank. Upon mixing with the creek water, groundwater was diluted by factors between 11 and 50, and the pH of the mixture became neutral. Metals originating from the contaminated groundwater were removed in the creek in the following order: Fe > Al > Pb >> Cu > Mn > Zn = Cd. Pb and Cu continued to be removed from solution even as the creek passed adjacent to a tailings pile. In contrast, Zn concentrations in the creek increased adjacent to the tailings area, presumably as a result of the reemergence of the upgradient plume as the creek lost elevation. Below the tailings dam, contaminated creek water (400-800 mu g Zn/l) was diluted by both smaller side streams and a creek of equal flow. The presence of 3 distinctive water masses required the use of two tracers (dissolved Si and S) to distinguish between mixing and geochemical reactions. The removal of metals was greater during low flow conditions. Pb was removed to the greatest extent, falling below detection limits (0.5 mu g/l) at the first sampling location. Copper and Mn were removed to a lesser extent during low flow conditions and approached conservative behavior during high dow conditions. During a 5-km journey through two hydrological regimes, less than 10% of the dissolved Zn and Cd was lost. (C) 1997 Elsevier Science Ltd.
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页码:447 / 464
页数:18
相关论文
共 29 条
[1]  
[Anonymous], 8096 US GEOL SURV WA
[2]  
[Anonymous], 2015, SUPERBOB
[3]   METAL BEHAVIOR DURING SURFACE GROUNDWATER INTERACTION, SILVER-BOW CREEK, MONTANA [J].
BENNER, SG ;
SMART, EW ;
MOORE, JN .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1995, 29 (07) :1789-1795
[4]   MECHANISM OF IRON REMOVAL IN ESTUARIES [J].
BOYLE, EA ;
EDMOND, JM ;
SHOLKOVITZ, ER .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1977, 41 (09) :1313-1324
[5]   Kinetic and mineralogic controls on the evolution of groundwater chemistry and Sr-87/Sr-86 in a sandy silicate aquifer, northern Wisconsin, USA [J].
Bullen, TD ;
Krabbenhoft, DP ;
Kendall, C .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1996, 60 (10) :1807-1821
[6]   PROCESSES CONTROLLING METAL-ION ATTENUATION IN ACID-MINE DRAINAGE STREAMS [J].
CHAPMAN, BM ;
JONES, DR ;
JUNG, RF .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1983, 47 (11) :1957-1973
[7]  
Claassen H.C., 1985, 712F US GEOL SURV
[8]  
COKELET ED, 1985, J GEOPHYS RES, V90, P7297
[9]  
Davis John H, 1993, METALS GROUNDWATER, P223
[10]  
Dzombak D.A., 1990, SURFACE COMPLEXATION