4.5 Article

Demystifying mercury geochemistry in contaminated soil-groundwater systems with complementary mercury stable isotope, concentration, and speciation analyses

Journal

ENVIRONMENTAL SCIENCE-PROCESSES & IMPACTS
Volume 24, Issue 9, Pages 1406-1429

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1em00368b

Keywords

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Funding

  1. Austrian Science Fund (FWF) [I-3489-N28]
  2. German Research Foundation (DFG) [BI 734/17-1]
  3. National Sciences and Engineering Council of Canada (NSERC) postdoctoral fellowship

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Interpretation of Hg geochemistry can be challenging due to the complexity of Hg transformation processes. In this study, we demonstrate the improved interpretation of Hg geochemistry by combining Hg stable isotope analyses with established methods. This approach allows us to identify specific Hg transformation processes and trace their behavior in environmental systems.
Interpretation of mercury (Hg) geochemistry in environmental systems remains a challenge. This is largely associated with the inability to identify specific Hg transformation processes and species using established analytical methods in Hg geochemistry (total Hg and Hg speciation). In this study, we demonstrate the improved Hg geochemical interpretation, particularly related to process tracing, that can be achieved when Hg stable isotope analyses are complemented by a suite of more established methods and applied to both solid- (soil) and liquid-phases (groundwater) across two Hg2+-chloride (HgCl2) contaminated sites with distinct geological and physicochemical properties. This novel approach allowed us to identify processes such as Hg2+ (i.e., HgCl2) sorption to the solid-phase, Hg2+ speciation changes associated with changes in groundwater level and redox conditions (particularly in the upper aquifer and capillary fringe), Hg2+ reduction to Hg-0, and dark abiotic redox equilibration between Hg-0 and Hg(ii). Hg stable isotope analyses play a critical role in our ability to distinguish, or trace, these in situ processes. While we caution against the non-critical use of Hg isotope data for source tracing in environmental systems, due to potentially variable source signatures and overprinting by transformation processes, our study demonstrates the benefits of combining multiple analytical approaches, including Hg isotope ratios as a process tracer, to obtain an improved picture of the enigmatic geochemical behavior and fate of Hg at contaminated legacy sites.

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