Abstract
Mass-dependent fractionation (MDF) and mass-independent fractionation (MIF) of Hg isotopes provides a new tool for tracing Hg in contaminated environments such as mining sites, which represent major point sources of Hg pollution into surrounding ecosystems. Here, we present Hg isotope ratios of unroasted ore waste, calcine (roasted ore), and poplar leaves collected at a closed Hg mine (New Idria, CA, U.S.A.). Unroasted ore waste was isotopically uniform with δ202Hg values from -0.09 to 0.16‰ (±0.10‰, 2 SD), close to the estimated initial composition of the HgS ore (-0.26‰). In contrast, calcine samples exhibited variable δ202Hg values ranging from -1.91‰ to +2.10‰. Small MIF signatures in the calcine were consistent with nuclear volume fractionation of Hg isotopes during or after the roasting process. The poplar leaves exhibited negative MDF (-3.18 to -1.22‰) and small positive MIF values (Δ199Hg of 0.02 to 0.21‰). Sequential extractions combined with Hg isotope analysis revealed higher δ202Hg values for the more soluble Hg pools in calcines compared with residual HgS phases. Our data provide novel insights into possible in situ transformations of Hg phases and suggest that isotopically heavy secondary Hg phases were formed in the calcine, which will influence the isotope composition of Hg leached from the site.
Original language | English |
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Pages (from-to) | 6137-6145 |
Number of pages | 9 |
Journal | Environmental Science and Technology |
Volume | 47 |
Issue number | 12 |
DOIs | |
State | Published - 18 Jun 2013 |
Externally published | Yes |
ASJC Scopus subject areas
- General Chemistry
- Environmental Chemistry