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	<journal>
		<journal_title>Atmospheric Chemistry and Physics Discussions</journal_title>
		<journal_url>www.atmos-chem-phys-discuss.net</journal_url>
		<issn>1680-7367</issn>
		<eissn>1680-7375</eissn>
		<volume_number>9</volume_number>
		<issue_number>6</issue_number>
		<publication_year>2009</publication_year>
	</journal>
	<doi>10.5194/acpd-9-26673-2009</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/9/26673/2009/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/9/26673/2009/acpd-9-26673-2009.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/9/26673/2009/acpd-9-26673-2009.pdf</fulltext_pdf>
	<start_page>26673</start_page>
	<end_page>26695</end_page>
	<publication_date>2009-12-11</publication_date>
	<article_title content_type="html">Overview of mercury measurements in the Antarctic troposphere</article_title>
	<authors>
		<author numeration="1" affiliations="1">
			<name>A. Dommergue</name>
			<email>dommergue@lgge.obs.ujf-grenoble.fr</email>
		</author>
		<author numeration="2" affiliations="2">
			<name>F. Sprovieri</name>
		</author>
		<author numeration="3" affiliations="2">
			<name>N. Pirrone</name>
		</author>
		<author numeration="4" affiliations="3">
			<name>R. Ebinghaus</name>
		</author>
		<author numeration="5" affiliations="4">
			<name>S. Brooks</name>
		</author>
		<author numeration="6" affiliations="1">
			<name>J. Courteaud</name>
		</author>
		<author numeration="7" affiliations="1">
			<name>C. Ferrari</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Laboratoire de Glaciologie et Géophysique de l&apos;Environnement, CNRS &amp;ndash;  Université Joseph Fourier Grenoble, 54 Rue Molière, 38400 St Martin d&apos;Hères, France</affiliation>
		<affiliation numeration="2" content_type="html">CNR &amp;ndash; Institute on Atmospheric Pollution Research, Division of Rende, Italy</affiliation>
		<affiliation numeration="3" content_type="html">GKSS Research Centre Geesthacht, Institute for Coastal Research, Max-Planck-Str. 1, 21502 Geesthacht, Germany</affiliation>
		<affiliation numeration="4" content_type="html">NOAA Air Resources Laboratory, Atmospheric Turbulence and Diffusion Division, USA</affiliation>
	</affiliations>
	<abstract content_type="html">Polar ecosystems are considered to be the last pristine environments
      of the Earth relatively uninfluenced by human activities. Antarctica
      in particular, compared to the Arctic is considered to be even less
      affected by any kind of anthropogenic influences. Once contaminants
      reach the polar regions, their lifetime in the troposphere depends on
      local removal processes. Atmospheric mercury, in particular, has
      unique characteristics that include long-range transport to polar
      regions and the transformation to more toxic and water-soluble
      compounds that may potentially become bioavailable. These
      chemical-physical properties have given mercury on the priority list
      of an increasing number of international, European and national
      conventions and agreements aimed at the protection of the ecosystems
      including human health (i.e., GEO, UNEP, AMAP, UN-ECE, HELCOM, OSPAR)
      thus stimulating a significant amount of research including
      measurements of Hg&lt;sup&gt;0&lt;/sup&gt; reaction rate constant with atmospheric
      oxidants, experimental and modelling studies in order to understand
      the cycling of Hg in polar regions and its impact to these
      ecosystems. Special attention in terms of contamination of polar
      regions, is paid to the consequences of the springtime phenomena,
      referred to as &apos;&apos;atmospheric mercury depletion event&apos;&apos; (AMDE),
      during which elemental gaseous mercury (GEM or Hg&lt;sup&gt;0&lt;/sup&gt;) through
      a series of photochemically-initiated reactions involving halogens,
      may be converted to a reactive form that may accumulate in polar
      ecosystems. The discovery of the AMDE, first noted in the Arctic, has
      also been observed at both poles and was initially considered to
      result in an important net input of atmospheric Hg into the polar
      surfaces. However, recent studies point out that complex processes
      take place after deposition that may result in less significant
      net-inputs from the atmosphere since a fraction, sometimes significant
      of deposited Hg may be recycled. Therefore, the contribution of this
      unique reactivity occurring in polar atmospheres to the global budget
      of atmospheric Hg and the role played by snow and ice surfaces of
      these regions are important issues. This paper presents a review of
      atmospheric mercury studies conducted in the Antarctic troposphere,
      both at coastal locations and on the Antarctic Plateau since 1985. Our
      current understanding of atmospheric reactivity in this region is also
      presented.</abstract>
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