Dynamic oxidation of gaseous mercury in the Arctic troposphere at polar sunrise

被引:425
作者
Lindberg, SE
Brooks, S
Lin, CJ
Scott, KJ
Landis, MS
Stevens, RK
Goodsite, M
Richter, A
机构
[1] Oak Ridge Natl Lab, Div Environm Sci, Oak Ridge, TN 37831 USA
[2] Oak Ridge Associated Univ, Oak Ridge, TN 37831 USA
[3] Lamar Univ, Dept Civil Engn, Beaumont, TX 77710 USA
[4] Univ Manitoba, Dept Microbiol, Winnipeg, MB R3T 2N2, Canada
[5] US EPA, Human Exposure Anal Branch, Res Triangle Pk, NC 27711 USA
[6] Florida Dept Environm Protect, Tallahassee, FL 32399 USA
[7] Natl Environm Res Inst Denmark, Copenhagen, Denmark
[8] Univ Bremen, Inst Environm Phys, D-28359 Bremen, Germany
关键词
D O I
10.1021/es0111941
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Gaseous elemental mercury (Hg-0) is a globally distributed air toxin with a long atmospheric residence time. Any process that reduces its atmospheric lifetime increases its potential accumulation in the biosphere. Our data from Barrow, AK, at 71degrees N show that rapid, photochemically driven oxidation of boundary-layer Hg-0 after polar sunrise, probably by reactive halogens, creates a rapidly depositing species of oxidized gaseous mercury in the remote Arctic troposphere at concentrations in excess of 900 pg m(-3). This mercury accumulates in the snowpack during polar spring at an accelerated rate in a form that is bioavailable to bacteria and is released with snowmelt during the summer emergence of the Arctic ecosystem. Evidence suggests that this is a recent phenomenon that may be occurring throughout the earth's polar regions.
引用
收藏
页码:1245 / 1256
页数:12
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