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A mass balance inventory of mercury in the Arctic Ocean

A mass balance inventory of mercury in the Arctic Ocean Environmental context. Mercury (Hg) occurs at high concentrations in Arctic marine wildlife, posing a possible health risk to northern peoples who use these animals for food. We find that although the dramatic Hg increases in Arctic Ocean animals since pre-industrial times can be explained by sustained small annual inputs, recent rapid increases probably cannot, because of the existing large oceanic Hg reservoir (the ‘flywheel’ effect). Climate change is a possible alternative force underpinning recent trends. Abstract. The present mercury (Hg) mass balance was developed to gain insights into the sources, sinks and processes regulating biological Hg trends in the Arctic Ocean. Annual total Hg inputs (mainly wet deposition, coastal erosion, seawater import, and ‘excess’ deposition due to atmospheric Hg depletion events) are nearly in balance with outputs (mainly shelf sedimentation and seawater export), with a net 0.3% year –1 increase in total mass. Marine biota represent a small fraction of the ocean’s existing total Hg and methyl-Hg (MeHg) inventories. The inertia associated with these large non-biological reservoirs means that ‘bottom-up’ processes (control of bioavailable Hg concentrations by mass inputs or Hg speciation) are probably incapable of explaining recent biotic Hg trends, contrary to prevailing opinion. Instead, varying rates of bioaccumulation and trophic transfer from the abiotic MeHg reservoir may be key, and are susceptible to ecological, climatic and biogeochemical influences. Deep and sustained cuts to global anthropogenic Hg emissions are required to return biotic Hg levels to their natural state. However, because of mass inertia and the less dominant role of atmospheric inputs, the decline of seawater and biotic Hg concentrations in the Arctic Ocean will be more gradual than the rate of emission reduction and slower than in other oceans and freshwaters. Climate warming has likely already influenced Arctic Hg dynamics, with shrinking sea-ice cover one of the defining variables. Future warming will probably force more Hg out of the ocean’s euphotic zone through greater evasion to air and faster Hg sedimentation driven by higher primary productivity; these losses will be countered by enhanced inputs from coastal erosion and rivers. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Environmental Chemistry CSIRO Publishing

A mass balance inventory of mercury in the Arctic Ocean

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References (146)

Publisher
CSIRO Publishing
Copyright
CSIRO
ISSN
1448-2517
eISSN
1449-8979
DOI
10.1071/EN08002
Publisher site
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Abstract

Environmental context. Mercury (Hg) occurs at high concentrations in Arctic marine wildlife, posing a possible health risk to northern peoples who use these animals for food. We find that although the dramatic Hg increases in Arctic Ocean animals since pre-industrial times can be explained by sustained small annual inputs, recent rapid increases probably cannot, because of the existing large oceanic Hg reservoir (the ‘flywheel’ effect). Climate change is a possible alternative force underpinning recent trends. Abstract. The present mercury (Hg) mass balance was developed to gain insights into the sources, sinks and processes regulating biological Hg trends in the Arctic Ocean. Annual total Hg inputs (mainly wet deposition, coastal erosion, seawater import, and ‘excess’ deposition due to atmospheric Hg depletion events) are nearly in balance with outputs (mainly shelf sedimentation and seawater export), with a net 0.3% year –1 increase in total mass. Marine biota represent a small fraction of the ocean’s existing total Hg and methyl-Hg (MeHg) inventories. The inertia associated with these large non-biological reservoirs means that ‘bottom-up’ processes (control of bioavailable Hg concentrations by mass inputs or Hg speciation) are probably incapable of explaining recent biotic Hg trends, contrary to prevailing opinion. Instead, varying rates of bioaccumulation and trophic transfer from the abiotic MeHg reservoir may be key, and are susceptible to ecological, climatic and biogeochemical influences. Deep and sustained cuts to global anthropogenic Hg emissions are required to return biotic Hg levels to their natural state. However, because of mass inertia and the less dominant role of atmospheric inputs, the decline of seawater and biotic Hg concentrations in the Arctic Ocean will be more gradual than the rate of emission reduction and slower than in other oceans and freshwaters. Climate warming has likely already influenced Arctic Hg dynamics, with shrinking sea-ice cover one of the defining variables. Future warming will probably force more Hg out of the ocean’s euphotic zone through greater evasion to air and faster Hg sedimentation driven by higher primary productivity; these losses will be countered by enhanced inputs from coastal erosion and rivers.

Journal

Environmental Chemistry – CSIRO Publishing

Published: Apr 17, 2008

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