Abstract

Environmental mercury (Hg) loads do not always correspond to Hg concentrations in resident fish and selenium (Se) presence has been reported to play a pivotal role in mitigating Hg bioaccumulation. Total mercury (THg), methylmercury (MeHg) and Se concentrations were measured in sediments and a benthic fish species (Platycephalus bassensis) from a contaminated estuary (Derwent Estuary, Tasmania). Elevated sediment concentrations of Se did not result in increased Se concentrations in fish, but low concentrations of Se were associated with increased MeHg bioavailability (% MeHg) from sediments to fish. Where MeHg (≈99% of total Hg) concentration in fish was high Se uptake also increased, indicating that maintaining positive Se:Hg ratios may reduce the toxicity of MeHg. MeHg was detectable in sediments throughout the estuary, and a molar excess of THg over Se suggested that there was insufficient Se to prevent methylation from the sediments. Se:Hg ratios of less than 1.0 in sediments, coupled with high %MeHg fraction and high biotic sediment accumulation factors for MeHg (BSAFMeHg), indicated that the lower region of the Derwent Estuary could be a hotspot for Hg methylation, despite having significantly lower THg concentrations. In contrast, Hg bioavailability to fish from sediments close to the source may be reduced by both inorganic Hg species complexation and lower methylation rates. There was a strong association between THg and Se in estuarine sediments, suggesting that Se plays an important role in sediment Hg cycling and should be a key consideration in any future assessments of Hg methylation, bioavailability and bioaccumulation.

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