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Title: Mercury Adsorption on Minerals and Its Effect on Microbial Methylation

Journal Article · · ACS Earth and Space Chemistry
ORCiD logo [1];  [2]; ORCiD logo [2]; ORCiD logo [3]; ORCiD logo [2]; ORCiD logo [4]
  1. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Environmental Sciences Division; Univ. of Illinois, Urbana-Champaign, IL (United States). Prairie Research Inst.
  2. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Environmental Sciences Division
  3. Pacific Northwest National Lab. (PNNL), Richland, WA (United States)
  4. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Environmental Sciences Division; Univ. of Tennessee, Knoxville, TN (United States). Dept. of Biosystems Engineering and Soil Science

Adsorbed or solid-phase inorganic mercury [Hg(II)] is commonly assumed immobile or less bioavailable for microbial uptake, although recent studies suggest that mineral-adsorbed Hg(II) is at least partially available for cell uptake and methylation. This study examined the adsorption of Hg(II) onto two reference minerals, hematite and montmorillonite, and evaluated Hg(II) uptake and methylation by a sulfate-reducing bacterium Desulfovibrio desulfuricans ND132 in laboratory incubations. Mineral-adsorbed Hg(II) on both hematite and montmorillonite was not only available for cell uptake and methylation but also resulted in a 2–3-fold increased methylmercury production compared to the mineral-free incubation. An optimal Hg(II) methylation was observed at a low to moderate mineral/solution ratio (1–5 g L–1) with fixed Hg(II) (25 nM) and cell concentrations. The result could be explained by decreased cellular immobilization of Hg(II) but enhanced close interactions between Hg(II) and cells both adsorbed or concentrated on mineral surfaces, leading to increased methylation. However, a high mineral/solution ratio inhibited Hg(II) methylation, likely as a result of a low Hg(II) coverage (per surface area) at high mineral loadings, which limit close contacts between Hg(II) and the cells. These results indicate that mineral-adsorbed Hg(II) may be directly available for microbial uptake or methylation, although whether the adsorption enhances or inhibits Hg(II) methylation may depend upon microniches, where Hg(II), microbes, and minerals co-exist in the natural environment. We suggest that future studies are performed to establish quantitative relationships of bioavailable Hg(II) with not only the dissolved but also adsorbed Hg(II) species to improve model predictions of Hg(II) fate and transformations.

Research Organization:
Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Biological and Environmental Research (BER)
Grant/Contract Number:
AC05-00OR22725
OSTI ID:
1559685
Journal Information:
ACS Earth and Space Chemistry, Vol. 3, Issue 7; ISSN 2472-3452
Publisher:
American Chemical SocietyCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 12 works
Citation information provided by
Web of Science