Mercury speciation in sediments at a municipal sewage sludge marine disposal site

Mercury speciation was performed in excess activated sewage sludge (ASS) and in marine sediments collected at the AAS disposal site off the Mediterranean coast of Israel in order to characterize the spatial and vertical distribution of different mercury species and assess their environmental impact. Total Hg (HgT) concentrations ranged between 0.19 and 1003 ng/g at the polluted stations and 5.7 and 72.8 ng/g at the background station, while the average concentration in ASS was 1181 ± 273 ng/g. Only at the polluted stations did HgT concentrations decrease exponentially with sediment depth, reaching background values at 16–20 cm, the vertical distribution resulting from mixing of natural sediment with ASS solids and bioturbation by large populations of polycheates.Average Methyl Hg (MeHg) concentration in ASS was 39.7 ± 7.1 ng/g, ca. 3% of the HgT concentration, while the background concentrations ranged between 0.1 and 0.61 ng/g. MeHg concentrations in surficial polluted sediments were 0.7–5.9 ng/g (ca. 0.5% of the HgT) and decreased vertically, similar to HgT. A positive correlation between MeHg and Hg only at the polluted stations, higher MeHg concentrations at the surface of the sediment and not below the redoxline, and no seasonality in the concentrations suggest that the MeHg originated from the ASS and not from in situ methylation. By doing selective extractions, we found that ca. 80% of the total Hg in ASS and polluted sediments was strongly bound to amorphous organo-sulfur and to inorganic sulfide species that are not bioavailable. The fractions with potential bioaccessible Hg had maximal concentrations in the range in which biotic effects should be expected. Therefore, although no bioaccumulation was found in the biota in the area, the concentration in the polluted sediments are not negligible and should be carefully monitored.