Mercury in the snow and firn at Summit Station, Central Greenland, and implications for the study of past atmospheric mercury levels

被引:38
作者
Fain, X. [1 ]
Ferrari, C. P. [1 ,4 ,7 ]
Dommergue, A. [1 ,4 ]
Albert, M. [2 ]
Battle, M. [3 ]
Arnaud, L. [1 ]
Barnola, J. -M. [1 ]
Cairns, W. [5 ]
Barbante, C. [5 ]
Boutron, C. [1 ,6 ,7 ]
机构
[1] Univ Grenoble 1, Lab Glaciol & Geophys Environm, CNRS, UMR 5183, F-38402 St Martin Dheres, France
[2] ERDC Cold Reg Res & Engn Lab, Geophys Sci Div, Hanover, NH 03755 USA
[3] Bowdoin Coll, Dept Phys & Astron, Brunswick, ME 04011 USA
[4] Univ Grenoble 1, F-38041 Grenoble, France
[5] Univ Venice, Dept Environm Sci, I-30123 Venice, Italy
[6] Univ Grenoble 1, Unite Format & Rech Phys, F-38041 Grenoble, France
[7] Inst Univ France, F-75005 Paris, France
关键词
D O I
10.5194/acp-8-3441-2008
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 (Ho degrees or GEM) was investigated at Summit Station. Greenland, in the interstitial air extracted from the perennial snowpack (firn) at depths ranging from the surface to 30m, during summer 2005 and spring 2006. Photolytic production and destruction of Hg degrees were observed close to the snow surface during summer 2005 and spring 2006, and we observed dark oxidation of GEM up to 270 cm depth in June 2006. Photochemical transformation of gaseous elemental mercury resulted in diel variations in the concentrations of this gas in the near-surface interstitial air. but destruction of Hg degrees was predominant in June, and production was the main process in July. This seasonal evolution of the chemical mechanisms involving gaseous elemental mercury produces a signal that propagates downward through the firn air, but is unobservably small below 15 m in depth. As a consequence, multi-annual averaged records of GEM concentration should be well preserved in deep firn air at depths below 15 m, and available for the reconstruction of the past atmospheric history of GEM over the last decades.
引用
收藏
页码:3441 / 3457
页数:17
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