Publication | Open Access
Mercury biogeochemical cycling in a stratified estuary
202
Citations
22
References
1993
Year
EngineeringOcean PollutionMarine ChemistryMixed LayerEnvironmental ChemistryMercury BiogeochemistryEnvironmental MicrobiologyTotal HgBiogeochemistryMercury Biogeochemical CyclingSediment-water InteractionWater QualityEcotoxicologyMercury ChemistryEstuarine GeochemistryParticulate ScavengingEnvironmental ToxicologyCoastal GeochemistryEstuary
Total Hg in the permanently stratified Pettaquamscutt estuary was <25 pM throughout the water column, even in highly sulfidic bottom waters. Particulate Hg was typically >40% of the total Hg. Reactive Hg (HgR) was generally <3 pM and decreased with depth, but there is HgR even in the anoxic bottom waters. Elemental Hg (Hg0) was highest in the mixed layer and below the detection limit at depth. Demethylation is not an important source of Hg0 in this estuary. Dimethylmercury was not detected. Monomethylmercury (MMHg) was near the detection limit in the mixed layer and increased rapidly in the low oxygen region. Dissolved MMHg correlated with bacteriochlorophyll pigments, suggesting that the microbial community plays an important role in MMHg production in this estuary. The overall distributions of dissolved and particulate Hg species result from the interaction with Fe and Mn redox cycling, particulate scavenging and sinking, and MMHg production in the pycnocline. The estimated rate of MMHg production from HgR in the pycnocline region is 1.7% d−1. Hg0 and MMHg are formed principally in the mixed layer and in the pycnocline region, respectively. Particulate scavenging is important, and sedimentation, methylation, and Hg0 production are the principal sinks for Hgr.
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