Diel changes in water chemistry in an arsenic-rich stream and treatment-pond system

被引:34
作者
Gammons, Chnistopher H. [1 ]
Grant, Tracy M.
Nimick, David A.
Parker, Stephen R.
DeGrandpre, Mike D.
机构
[1] Montana Tech Univ Montana, Dept Geol Engn, Butte, MT 59701 USA
[2] Montana Tech Univ Montana, Dept Chem & Geochem, Butte, MT 59701 USA
[3] US Geol Survey, Helena, MT USA
[4] Univ Montana, Dept Chem, Missoula, MT 59812 USA
基金
美国国家科学基金会;
关键词
geochemistry; diel; diurnal; adsorption; superfund; Clark Fork River; Montana; manganese; arsenic; heavy metals;
D O I
10.1016/j.scitotenv.2007.06.029
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Arsenic concentrations are elevated in surface waters of the Warm Springs Ponds Operable Unit (WSPOU), located at the head of the upper Clark Fork River Superfund site, Montana, USA. Arsenic is derived from historical deposition of smelter emissions (Mill and Willow Creeks) and historical mining and milling wastes (Silver Bow Creek). Although long-term monitoring has characterized the general seasonal and flow-related trends in As concentrations in these streams and the pond system used to treat Silver Bow Creek water, little is known about solubility controls and sorption processes that influence diel cycles in As concentrations. Diel (24-h) sampling was conducted in July 2004 and August 2005 at the outlet of the treatment ponds, at two locations along a nearby reconstructed stream channel that diverts tributary water around the ponds, and at Silver Bow Creek 2 km below the ponds. Dissolved As concentration increased up to 51% during the day at most of the stream sites, whereas little or no diel change was displayed at the treatment-pond outlet. The strong cycle in streams is explained by pH- and temperature-dependent sorption of As onto hydrous metal oxides or biofilms on the streambed. Concentrations of dissolved Ca2+ and HCO3- at the stream sites showed a diel temporal pattern opposite to that of As, and geochemical modeling supports the hypothesis that the concentrations of Ca2+ and HCO3- were controlled by precipitation of calcite during the warm afternoon hours when pH rose above 9.0. Nightly increases in dissolved Mn and Fe(II) concentrations were out of phase with concentrations of other divalent cations and are more likely explained by redox phenomena. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:433 / 451
页数:19
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