Uranium stability in a large wetland soil core probed by electron acceptors, carbonate amendments and wet-dry cycling in a long-term lysimeter experiment

Understanding the hydro-biogeochemical conditions that impact the mobility of uranium (U) in natural or artificial wetlands is essential for the management of contaminated environments. Field-based research indicates that high organic matter content and saturation of the soil from the water table create favorable conditions for U accumulation. Despite the installation of artificial wetlands for U remediation, the processes that can release U from wetland soils to underlying aquifers are poorly understood. Here we used a large soil core from a montane wetland in a 6 year lysimeter experiment to study the stability of U accumulated to levels of up to 6000 ppm. Amendments with electron acceptors showed that the wetland soil can reduce sulfate and Fe(III) in large amounts without significant release of U into the soil pore water. However, amendment with carbonate (5 mM, pH 7.5) resulted in a large discharge of U. After a six-month period of imposed drought, the re-flooding of the core led to the release of negligible amounts of U into the pore water. This long-term experiment demonstrates that U is strongly bound to organic matter and that its stability is only challenged by carbonate complexation. [Display omitted] •Uranium accumulates to an exceptional level in a montane wetland of the Swiss Alps.•Amendments of the soil with redox species such as NO3− and SO42− do not desorb U.•A long period of drought followed by flooding does not desorbed U from the soil.•The stability of U in the wetland is only challenged by carbonates amendment.