Circumpolar measurements of speciated mercury, ozone and carbon monoxide in the boundary layer of the Arctic Ocean
International audience Using the Swedish icebreaker Oden as a platform, continuous measurements of airborne mercury (gaseous elemental mercury (Hg0), divalent gaseous mercury species HgIIX2(g) (acronym RGM) and mercury attached to particles (PHg)) and some long-lived trace gases (carbon monoxide CO...
Published in: | Atmospheric Chemistry and Physics |
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Main Authors: | , , |
Other Authors: | , , , , , , , , , , |
Format: | Article in Journal/Newspaper |
Language: | English |
Published: |
HAL CCSD
2010
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Subjects: | |
Online Access: | https://insu.hal.science/insu-00554371 https://insu.hal.science/insu-00554371/document https://insu.hal.science/insu-00554371/file/acp-10-5031-2010.pdf https://doi.org/10.5194/acp-10-5031-2010 |
Summary: | International audience Using the Swedish icebreaker Oden as a platform, continuous measurements of airborne mercury (gaseous elemental mercury (Hg0), divalent gaseous mercury species HgIIX2(g) (acronym RGM) and mercury attached to particles (PHg)) and some long-lived trace gases (carbon monoxide CO and ozone O3) were performed over the North Atlantic and the Arctic Ocean. The measurements were performed for nearly three months (July-September 2005) during the Beringia 2005 expedition (from Göteborg, Sweden via the proper Northwest Passage to the Beringia region Alaska - Chukchi Penninsula - Wrangel Island and in-turn via a north-polar transect to Longyearbyen, Spitsbergen). The Beringia 2005 expedition was the first time that these species have been measured during summer over the Arctic Ocean going from 60° to 90° N. During the North Atlantic transect, concentration levels of Hg0, CO and O3 were measured comparable to typical levels for the ambient mid-hemispheric average. However, a rapid increase of Hg0 in air and surface water was observed when entering the ice-covered waters of the Canadian Arctic archipelago. Large parts of the measured waters were supersaturated with respect to Hg0, reflecting a strong disequilibrium. Heading through the sea ice of the Arctic Ocean, a fraction of the strong Hg0 pulse in the water was transferred with some time-delay into the air samples collected ~20 m above sea level. Several episodes of elevated Hg0 in air were encountered along the sea ice route with higher mean concentration (1.81±0.43 ng m−3) compared to the marine boundary layer over ice-free Arctic oceanic waters (1.55±0.21 ng m−3). In addition, the bulk of the variance in the temporal series of Hg0 concentrations was observed during July. The Oden Hg0 observations compare in this aspect very favourably with those at the coastal station Alert. Atmospheric boundary layer O3 mixing ratios decreased when initially sailing northward. In the Arctic, an O3 minimum around 15-20 ppbV was observed during summer ... |
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