TY - JOUR
T1 - Selenium isotope ratios as indicators of selenium sources and oxyanion reduction
AU - Johnson, Thomas M.
AU - Herbel, Mitchell J.
AU - Bullen, Thomas D.
AU - Zawislanski, Peter T.
N1 - Funding Information:
This work was supported by the National Science Foundation, Division of Earth Sciences, Hydrologic Sciences Program under grant EAR 97-25799, by the Assistant Secretary for Fossil Energy, National Petroleum Technology Office, of the U.S. Department of Energy, under contract DE-AC03-67SF00098, and by the San Francisco Bay Regional Water Quality Control Board. We thank T. Fan, Y. Zhang, and G. Frankenberger for providing samples from their Se transformation experiments, D. J. DePaolo and T. Owens for assistance with the double isotope spike calculations, and K. Tanji for advice in various aspects of the project. Helpful reviews by A. D. Anbar and an anonymous reviewer significantly improved the manuscript.
PY - 1999/9
Y1 - 1999/9
N2 - Selenium stable isotope ratio measurements should serve as indicators of sources and biogeochemical transformations of Se. We report measurements of Se isotope fractionation during selenate reduction, selenite sorption, oxidation of reduced Se in soils, and Se volatilization by algae and soil samples. These results, combined with previous work with Se isotopes, indicate that reduction of soluble oxyanions is the dominant cause of Se isotope fractionation. Accordingly, Se isotope ratios should be useful as indicators of oxyanion reduction, which can transform mobile species to forms that are less mobile and less bioavailable. Additional investigations of Se isotope fractionation are needed to confirm this preliminary assessment. We have developed a new method for measurement of natural Se isotope ratio variation which requires less than 500 ng Se per analysis and yields ±0.2‰ precision on 80Se/76Se. A double isotope spike technique corrects for isotopic fractionation during sample preparation and mass spectrometry. The small minimum sample size is important, as Se concentrations are often below 1 ppm in solids and 1 μg/L in fluids. The Se purification process is rapid and compatible with various sample matrices, including acidic rock or sediment digests.
AB - Selenium stable isotope ratio measurements should serve as indicators of sources and biogeochemical transformations of Se. We report measurements of Se isotope fractionation during selenate reduction, selenite sorption, oxidation of reduced Se in soils, and Se volatilization by algae and soil samples. These results, combined with previous work with Se isotopes, indicate that reduction of soluble oxyanions is the dominant cause of Se isotope fractionation. Accordingly, Se isotope ratios should be useful as indicators of oxyanion reduction, which can transform mobile species to forms that are less mobile and less bioavailable. Additional investigations of Se isotope fractionation are needed to confirm this preliminary assessment. We have developed a new method for measurement of natural Se isotope ratio variation which requires less than 500 ng Se per analysis and yields ±0.2‰ precision on 80Se/76Se. A double isotope spike technique corrects for isotopic fractionation during sample preparation and mass spectrometry. The small minimum sample size is important, as Se concentrations are often below 1 ppm in solids and 1 μg/L in fluids. The Se purification process is rapid and compatible with various sample matrices, including acidic rock or sediment digests.
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U2 - 10.1016/S0016-7037(99)00279-3
DO - 10.1016/S0016-7037(99)00279-3
M3 - Article
AN - SCOPUS:0033428347
SN - 0016-7037
VL - 63
SP - 2775
EP - 2783
JO - Geochimica et Cosmochimica Acta
JF - Geochimica et Cosmochimica Acta
IS - 18
ER -