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Dep. of Soil, Water and Climate, Univ. of Minnesota, 1991 Upper Buford Circle, St. Paul, MN 55108;
Dep. of Agronomy, Kansas State Univ.;
Soil Science Dep., Univ. of Wisconsin, Madison WI 53706.
* Corresponding author (ulf.skyllberg{at}sek.slu.se).
ABSTRACT
The binding of Hg2+ in organic matter of soils and waters controls the transport and transformations of Hg in terrestrial and aquatic ecosystems. We developed a competitive complexation method using the strong complexation of Hg2+ by Br– for determining the Hg2+ binding strength in organic soils at native and elevated Hg concentrations. The distribution coefficients determined in KBr suspensions for sorption of native Hg2+ to soil organic carbon (SOC) (KSOC) are in the range of 1022 to 1023. The KSOC significantly decreased with increased additions of Hg2+ and with decreasing pH. Using data for reduced organic S concentrations determined by x-ray absorption near-edge structure spectroscopy (XANES), we calculated surface complex formation constants on the order of 1032 for a model site having acidity constants of mercaptoacetic acid. This value is in fair agreement with the tabulated value of 10345 for Hg2+ binding in mercaptoacetic acid. At native Hg concentrations, formation constants and KSOC values were similar for different types of soil organic matter along transects from uplands into wetlands, despite varying concentrations of Hg and reduced organic S. Our adsorption data are consistent with the conclusions from our previous extended x-ray absorption fine structure spectroscopy (EXAFS) study that in a humic acid and soil, Hg2+ ions bond in two-fold coordination involving one reduced S and one O or N.
U. Skyllberg present address: Dep. of Forest Ecology, Swedish Univ. of Agricultural Sciences, S-901 83 Umeå, Sweden.
Received for publication April 13, 1999.
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