Assessing mine drainage pH from the color and spectral reflectance of chemical precipitates

被引:52
|
作者
Williams, DJ
Bigham, JM
Cravotta, CA
Traina, SJ
Anderson, JE
Lyon, JG
机构
[1] Ohio State Univ, Dept Civil & Environm Engn & Geodet Sci, Columbus, OH 43210 USA
[2] Coll William & Mary, Sch Marine Sci, Virginia Inst Marine Sci, Gloucester Point, VA 23062 USA
[3] US Geol Survey, Div Water Resources, New Cumberland, PA 17070 USA
[4] Ohio State Univ, Sch Nat Resources, Columbus, OH 43210 USA
关键词
D O I
10.1016/S0883-2927(02)00019-7
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 pH of mine impacted waters was estimated from the spectral reflectance of resident sediments composed mostly of chemical precipitates. Mine drainage sediments were collected from sites in the Anthracite Region of eastern Pennsylvania, representing acid to near neutral pH. Sediments occurring in acidic waters contained primarily schwertmannite and goethite while near neutral waters produced ferrihydrite. The minerals comprising the sediments occurring at each pH mode were spectrally separable. Spectral angle difference mapping was used to correlate sediment color with stream water pH (r(2)=0.76). Band-center and band-depth analysis of spectral absorption features were also used to discriminate ferrihydrite and goethite and/or schwertmannite by analyzing the T-4(1)<--(6)A(1) crystal field transition (9001000 nm). The presence of these minerals accurately predicted stream water pH (r(2)=0.87) and provided a qualitative estimate of dissolved SO4 concentrations. Spectral analysis results were used to analyze airborne digital multispectral video (DMSV) imagery for several sites in the region. The high spatial resolution of the DMSV sensor allowed for precise mapping of the mine drainage sediments. The results from this study indicate that airborne and space-borne imaging spectrometers may be used to accurately classify streams impacted by acid vs. neutral-to-alkaline mine drainage after appropriate spectral libraries are developed. Published by Elsevier Science Ltd.
引用
收藏
页码:1273 / 1286
页数:14
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