Extraction and distribution of soil organic and inorganic selenium in coal mine environments of Wyoming, USA

Abstract

 Selenium (Se), an animal toxicant and aquifer contaminant, occurs in coal mine environments of Wyoming. There is a paucity of information on solution-phase Se speciation in mine soils. The objectives of this study were to compare Se extraction efficiencies of various reagents and to characterize SeO^2– ₃ (selenite), SeO^2– ₄ (selenate) and organic Se components in these extracts. Forty coal mine soils were extracted using DI (deionized) water, hot water (0.1% CaCl₂), AB-DTPA, NaOH, and KH₂PO₄. Each solution was analyzed for total dissolved Se, and inorganic and organic Se fractions. Both inorganic and organic Se fractions were detected in the soil extracts. The order of Se (total, inorganic, and organic) extraction efficiency for different reagents was DI water < hot water < AB-DTPA < NaOH < KH₂PO₄. The inorganic–organic Se ratios in DI water, hot water, AB-DTPA, NaOH, and KH₂PO₄ extracts were 60 : 40, 26 : 74, 61 : 39, 87 : 13, and 52 : 48, respectively, indicating predominance of inorganic Se in all but the hot water extract. Selenite was the dominant inorganic species in AB-DTPA and KH₂PO₄ extracts, while SeO^2– ₄ was the major Se species in the DI water, hot water, and NaOH extracts. Significant correlations (P<0.01) were observed among extractable inorganic Se [NaOH and KH₂PO₄ (r=0.95); hot water and AB-DTPA (r=0.89)], total soluble Se [DI water with hot water (r=0.98) and AB-DTPA (r=0.95)], and Se species [SeO^2– ₃ in AB-DTPA with SeO^2– ₄ in NaOH (r=0.94) and SeO^2– ₃ in KH₂PO₄ (r=0.88)]. These correlations are indicative of Se extraction efficiency, thermodynamically predicted chemical transformations (such as oxidation of SeO^2– ₃ to SeO^2– ₄), and probable interconversions between the organic and inorganic Se fractions (r=0.70 in KH₂PO₄ extracts); as a whole the correlations can be used as statistical validations of possible geochemical processes.