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Deep anoxic aquifers could act as sinks for uranium through microbial-assisted mineral trapping

  • Ivan N. Pidchenko
  • , John N. Christensen
  • , Martin Kutzschbach
  • , Konstantin Ignatyev
  • , Ignasi Puigdomenech
  • , Eva Lena Tullborg
  • , Nick M.W. Roberts
  • , E. Troy Rasbury
  • , Paul Northrup
  • , Ryan Tappero
  • , Kristina O. Kvashnina
  • , Thorsten Schäfer
  • , Yohey Suzuki
  • , Henrik Drake
  • Linnaeus University
  • Lawrence Berkeley National Laboratory
  • Technical University of Berlin
  • Diamond Light Source
  • Swedish Nuclear Fuel and Waste Management Company
  • Terralogica AB
  • British Geological Survey
  • Brookhaven National Laboratory
  • Helmholtz-Zentrum Dresden-Rossendorf
  • European Synchrotron Radiation Facility
  • Friedrich Schiller University Jena
  • The University of Tokyo

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Uptake of uranium (U) by secondary minerals, such as carbonates and iron (Fe)-sulfides, that occur ubiquitously on Earth, may be substantial in deep anoxic environments compared to surficial settings due to different environment-specific conditions. Yet, knowledge of U reductive removal pathways and related fractionation between 238U and 235U isotopes in deep anoxic groundwater systems remain elusive. Here we show bacteria-driven degradation of organic constituents that influences formation of sulfidic species facilitating reduction of geochemically mobile U(VI) with subsequent trapping of U(IV) by calcite and Fe-sulfides. The isotopic signatures recorded for U and Ca in fracture water and calcite samples provide additional insights on U(VI) reduction behaviour and calcite growth rate. The removal efficiency of U from groundwater reaching 75% in borehole sections in fractured granite, and selective U accumulation in secondary minerals in exceedingly U-deficient groundwater shows the potential of these widespread mineralogical sinks for U in deep anoxic environments.

Original languageEnglish
Article number128
JournalCommunications Earth and Environment
Volume4
Issue number1
DOIs
StatePublished - Dec 2023

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