HR: 0800h
AN: B11B-0408    [Abstracts]
TI: Importance of Dissolved Neutral Hg-Sulfides, Energy Rich Organic Matter and total Hg Concentrations for Methyl Mercury Production in Sediments
AU: * Drott, A
EM: andreas.drott@sek.slu.se
AF: Swedish University of Agricultural Sciences, Department of Forest Ecology and Management, Umea, S-90183, Sweden
AU: Skyllberg, U
EM: ulf.skyllberg@sek.slu.se
AF: Swedish University of Agricultural Sciences, Department of Forest Ecology and Management, Umea, S-90183, Sweden
AB: Methyl mercury (MeHg) is the mercury form that biomagnifies to the greatest extent in aquatic food webs. Therefore information about factors determining MeHg concentrations is critical for accurate risk assessment of contaminated environments. The concentration of MeHg in wetlands and sediments is the net result of: 1) methylation rates, 2) demethylation rates, and 3) input/output processes. In this study, the main controls on Hg methylation rates and total concentrations of MeHg, were investigated at eight sites in Sweden with sediments that had been subjected to local Hg contamination either as Hg(0), or as phenyl-Hg. Sediments were selected to represent a gradient in total Hg concentration, temperature climate, salinity, primary productivity, and organic C content and quality. Most sediments were high in organic matter content due to wood fibre efflux from pulp and paper industry. The pore water was analysed for total Hg, MeHg, DOC, H₂S(aq), pH, DOC, Cl and Br. The chemical speciation of Hg(II) and MeHg in pore water was calculated using equilibrium models. Potential methylation and demethylation rates in sediments were determined in incubation experiments at 23° C under N2(g) for 48 h, after addition of isotopically enriched ²⁰¹Hg(II) and Me²⁰⁴Hg. In all surface (0-20 cm) sediments there was a significant (p<0.001) positive relationship between the experimentally determined specific potential methylation rate constant (K_m, day^-1) and % MeHg (concentrations of MeHg normalized to total Hg) in the sediment. This indicates that MeHg production overruled degradation and input/output processes of MeHg in surface sediments, and that % MeHg in surface sediments may be used as a proxy for net production of MeHg. To our knowledge, these are the first data showing significant positive relationships between short term (48 h) MeHg production and longer term accumulation of MeHg, across a range of sites with different properties (1). If MeHg was not normalized to total Hg, the relationship was not significant. For sub-sets of brackish waters (p<0.001, n=23), southern, high-productivity freshwaters (p<0.001, n=20) as well as northern, low-productivity freshwater (p=0.048, n=6), the sum of neutral Hg-sulfides [Hg(SH)2⁰ (aq)] and [HgS⁰ (aq)] in the sediment pore water was significantly, positively correlated with both the potential methylation rate constant (K_m) and total MeHg concentrations (2). This indicates that methylating sulphate reducing bacteria passively take up neutral Hg-sulfides, which are transformed to MeHg. Differences in slopes of the relationships were explained by differences in primary productivity and availability of energy-rich organic matter to methylating bacteria. High primary productivity at southern freshwater sites, reflected by a low C/N ratio (large contribution from free living algae and bacteria) in the sediment and a high annual temperature sum, resulted in high methylation rates. In conclusion, concentrations of neutral Hg-sulfides and availability of energy rich organic matter, but also total Hg concentrations in sediments are important factors behind net production and accumulation of MeHg . References: (1) Drott et. al. submitted, (2) Drott, A.; Lambertsson, L.; Björn, E.; Skyllberg, U. Importance of dissolved neutral mercury sulfides for methyl mercury production in contaminated sediments. Environmental Science & Technology 2007, 41, 2270-2276.
DE: 0414 Biogeochemical cycles, processes, and modeling (0412, 0793, 1615, 4805, 4912)
SC: Biogeosciences [B]
MN: 2007 Fall Meeting