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Uranium Repartitioning during Microbial Driven Reductive Transformation of U(VI)-Sorbed Schwertmannite and Jarosite
Department of Biology and Environmental Science, Linnaeus University, 39231 Kalmar, Sweden.
Centre for Ecology and Evolution in Microbial Model Systems (EEMiS), Linnaeus University, 39231 Kalmar, Sweden.
Department of Geosciences, Swedish Museum of Natural History, 10405 Stockholm, Sweden.
Canadian Light Source, 44 Innovation Boulevard, Saskatoon, SK S7N 2 V3, Canada.
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2024 (English)In: Environmental Science and Technology, ISSN 0013-936X, E-ISSN 1520-5851, Vol. 58, no 41, p. 18324-18334Article in journal (Refereed) Published
Abstract [en]

This study exposes U(VI)-sorbed schwertmannite and jarosite to biotic reductive incubations under field-relevant conditions and examines the changes in aqueous and solid-phase speciation of U, Fe, and S as well as associated microbial communities over 180 days. The chemical, X-ray absorption spectroscopy, X-ray diffraction, and microscopic data demonstrated that the U(VI)-sorbed schwertmannite underwent a rapid reductive dissolution and solid-phase transformation to goethite, during which the surface-sorbed U(VI) was partly reduced and mostly repartitioned to monomeric U(VI)/U(IV) complexes by carboxyl and phosphoryl ligands on biomass or organic substances. Furthermore, the microbial data suggest that these processes were likely driven by the consecutive developments of fermentative and sulfate- and iron- reducing microbial communities. In contrast, the U(VI)-sorbed jarosite only stimulated the growth of some fermentative communities and underwent very limited reductive dissolution and thus, remaining in its initial state with no detectable mineralogical transformation and solid-phase U reduction/repartitioning. Accordingly, these two biotic incubations did not induce increased risk of U reliberation to the aqueous phase. These findings have important implications for understanding the interactions of schwertmannite/jarosite with microbial communities and colinked behavior and fate of U following the establishment of reducing conditions in various acidic and U-rich settings.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2024. Vol. 58, no 41, p. 18324-18334
Keywords [en]
Uranium, X-ray absorption spectroscopy, acidic drainage, jarosite, microbial communities, schwertmannite
National Category
Earth and Related Environmental Sciences
Identifiers
URN: urn:nbn:se:oru:diva-116533DOI: 10.1021/acs.est.4c03645ISI: 001328597900001PubMedID: 39361056Scopus ID: 2-s2.0-85206403307OAI: oai:DiVA.org:oru-116533DiVA, id: diva2:1903369
Funder
Swedish Research Council Formas, 2020-01004UPPMAX, 2023/22-893; 2023/6-261Swedish Research Council, 2022-06725; 2018-05973
Note

This work was financially supported by the Swedish Research Council Formas (contracts 2020-01004 to C.Y.). We thank the Canadian Light Source (the BioXAS-Main beamline, 07ID-2 M) for providing beam time under proposal [33G11426]. Z.S. acknowledges financial support from the National Natural Science Foundation of China (42225101). M.D. further acknowledges the Science for Life Laboratory (SciLifeLab) and the National Genomics Infrastructure (NGI). Bioinformatics analyses were carried out utilizing the Uppsala Multidisciplinary Center for Advanced Computational Science (UPPMAX) at Uppsala University (projects NAISS 2023/22-893 & 2023/6-261). The computations were enabled by resources provided by the National Academic Infrastructure for Supercomputing in Sweden (NAISS) and the Swedish National Infrastructure for Computing (SNIC) at UPPMAX, Uppsala University partially funded by the Swedish Research Council through grant agreements no. 2022-06725 and no. 2018-05973.

Available from: 2024-10-04 Created: 2024-10-04 Last updated: 2025-02-07Bibliographically approved

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