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Published January 1, 2001 | public
Journal Article

The Importance of colloids for the behavior of uranium isotopes in the low-salinity zone of a stable estuary

Abstract

Particle-mediated removal processes of U isotopes were investigated during spring flood discharge in the low-salinity zone (LSZ, up to 3 practical salinity units [psu]) of a stable estuary. A shipboard ultrafiltration cross-flow filtration (CFF) technique was used to separate particles (>0.2 μm) and colloids (between 3000 daltons (3 kD) and 0.2 μm) from ultrafiltered water (<3 kD) containing "dissolved" species. Sediment traps were used to collect sinking material. Concentration of Fe and organic C, which are indicators of the major U carrier phases, were used to interpret the behavior of ^(234)U-^(238)U during estuarine mixing. Colloids dominated the river water transport of U, carrying ≈90% of the U. On entering the estuary, colloids accounted for the dominant fraction of U to about a salinity of 1 psu, but only a minor fraction (<5%) at 3 psu. A substantial fraction of the total U is removed at <1 psu by Fe-organic rich colloids that aggregate and sink during initial estuarine mixing in the Kalix River estuary. In contrast, at salinities >1 psu, there is a general correlation between U and salinity in all filtered fractions. The ^(234)U/^(238)U ratios in different filtered fractions and sinking particles were generally indistinguishable at each station and showed enrichment in ^(234)U, compared with secular equilibrium (δ^(234)U = 266–567). This clearly shows that all size fractions are dominated by nondetrital U. Consideration of U isotope systematics across the estuary reveals that substantial U exchange must occur involving larger particles at least to 1 psu and involving colloids at least to ≈1.5 psu. Further exchange at higher salinities may also occur, as the proportion of U on colloids decreases with increasing salinity. This may be due to decreasing colloid concentration and increasing stabilization of uranyl carbonate complexes during mixing in the estuary. The results show that although U is a soluble element that shows generally conservative mixing in estuaries, removal occurs in the very low salinity zone, and this zone represents a significant sink of U. Variation in composition and concentration of colloidal particles between different estuaries might thus be an important factor for determining the varying behavior of U between estuaries.

Additional Information

© 2001 Elsevier Science Ltd. Received November 16, 1999; accepted in revised form July 14, 2000. This work was supported by grants from the Swedish Natural Science Research Council (NFR, G/GU 0631-314, 315, and 316) to PSA and the U.S. Dept. of Energy (DOE, DE-FG03-88ER13851 to G.J.W. For assistance during sampling we gratefully acknowledge H. Holmström, A. Widerlund, and M. Zacher. We thank the crew of R/V KBV005 and Umeå Marine Research Center for assistance and collaboration during fieldwork. The reviewer's comments are much appreciated. This is CIT Div. Contr. No. 8608 (1025).

Additional details

Created:
August 19, 2023
Modified:
October 25, 2023