Effect of chemical pollution on forms of 137Cs, 90Sr and 239,240Pu in arctic soil studied by sequential extraction.

Abstract The aim of the present study was to determine the forms of 137 Cs, 90 Sr and 239,240 Pu occurring in different soil horizons using sequential extraction of samples taken from four sites located along a pollution gradient from the copper–nickel smelter at Monchegorsk in the Kola Peninsula, Russia, and from a reference site in Finnish Lapland in 1997. A selective sequential-leaching procedure was employed using a modification of the method of Tessier, Cambell and Bisson ((1979). Analytical Chemistry , 51 , 844–851). For 137 Cs the organic (O) and uppermost mineral (E1) layer were studied, for 90 Sr and 239,240 Pu only the uppermost organic layer (Of). The fraction of 137 Cs occurring in readily exchangeable form in the organic layer was about 50% at the reference site and decreased as a function of pollution, being 15% at the most polluted site in the Kola Peninsula. There was a clear positive correlation in the O layer between the distance from the smelter and the percentage of 137 Cs extracted in the readily exchangeable fraction (Spearman correlation r sp =0.7805, p =0.0001), whereas in the E1 layer no correlation was evident. The distribution of 90 Sr in the Of layer was similar at all sites, with the highest amounts occurring in exchangeable form and bound to organic matter, whereas stable Sr showed a somewhat different distribution with the highest amount in the oxide fraction. Most of the 239,240 Pu was bound to organic matter. Chemical pollution affected the exchangeable fraction of 239,240 Pu, which was about 1% at the most polluted site and 4–6% at the other sites.