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<front>
<journal-meta>
<journal-id journal-id-type="publisher">ACP</journal-id>
<journal-title-group>
<journal-title>Atmospheric Chemistry and Physics</journal-title>
<abbrev-journal-title abbrev-type="publisher">ACP</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">1680-7324</issn>
<publisher><publisher-name>Copernicus GmbH</publisher-name>
<publisher-loc>Göttingen, Germany</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.5194/acp-3-1871-2003</article-id>
<title-group>
<article-title>Gaseous (DMS, MSA, SO&lt;sub&gt;2&lt;/sub&gt;, H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt; and DMSO) and particulate (sulfate and methanesulfonate) sulfur species over the northeastern coast of Crete</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Bardouki</surname>
<given-names>H.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Berresheim</surname>
<given-names>H.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Vrekoussis</surname>
<given-names>M.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Sciare</surname>
<given-names>J.</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kouvarakis</surname>
<given-names>G.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Oikonomou</surname>
<given-names>K.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Schneider</surname>
<given-names>J.</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mihalopoulos</surname>
<given-names>N.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>Environmental Chemical Processes Laboratory (ECPL), Department of Chemistry, University of Crete, P.O Box 1470, 71409 Heraklion, Greece</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>Deutscher Wetterdienst (DWD), Meteorological Observatory, Hohenpeissenberg, Germany</addr-line>
</aff>
<aff id="aff3">
<label>3</label>
<addr-line>Max-Planck Institute for Chemistry, Biogeochemistry Division, Mainz, Germany</addr-line>
</aff>
<aff id="aff4">
<label>4</label>
<addr-line>now at LSCE, Orme des Merisiers, Bat 709, CE Saclay, 91191 Gif-sur-Yvette Cedex, France</addr-line>
</aff>
<pub-date pub-type="epub">
<day>31</day>
<month>10</month>
<year>2003</year>
</pub-date>
<volume>3</volume>
<issue>5</issue>
<fpage>1871</fpage>
<lpage>1886</lpage>
<permissions>
<license xlink:type="simple">
<license-p>This is an open-access article ditributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
</license>
</permissions>
<self-uri xlink:href="http://www.atmos-chem-phys.net/3/1871/2003/acp-3-1871-2003.html">This article is available from http://www.atmos-chem-phys.net/3/1871/2003/acp-3-1871-2003.html</self-uri>
<self-uri xlink:href="http://www.atmos-chem-phys.net/3/1871/2003/acp-3-1871-2003.pdf">The full text article is available as a PDF file from http://www.atmos-chem-phys.net/3/1871/2003/acp-3-1871-2003.pdf</self-uri>
<abstract>
<p>A detailed study of the levels, the temporal and diurnal variability of the main
      compounds involved in the biogenic sulfur cycle was carried out in Crete (Eastern
      Mediterranean) during the Mediterranean Intensive Oxidant Study (MINOS) field
      experiment in July-August 2001. Intensive measurements of gaseous dimethylsulfide
      (DMS), dimethylsulfoxide (DMSO), sulfur dioxide (SO&lt;sub&gt;2&lt;/sub&gt;), sulfuric
      (H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt;) and methanesulfonic acids (MSA) and particulate sulfate
      (SO&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;2-&lt;/sup&gt;) and methanesulfonate (MS&lt;sup&gt;-&lt;/sup&gt;) have been performed during the campaign.&lt;br&gt;
      &lt;br&gt;
      Dimethylsulfide (DMS) levels ranged from 2.9 to 136 pmol·mol&lt;sup&gt;-1&lt;/sup&gt; (mean value of
      21.7 pmol·mol&lt;sup&gt;-1&lt;/sup&gt;) and showed a clear diurnal variation with daytime maximum. During
      nighttime DMS levels fall close or below the detection limit of 2
      pmol·mol&lt;sup&gt;-1&lt;/sup&gt;. Concurrent measurements of OH and NO&lt;sub&gt;3&lt;/sub&gt; radicals during the campaign indicate that
      NO&lt;sub&gt;3&lt;/sub&gt; levels can explain most of the observed diurnal variation of DMS. Dimethylsulfoxide
      (DMSO) ranged between 0.02 and 10.1 pmol·mol&lt;sup&gt;-1&lt;/sup&gt; (mean value of
      1.7 pmol·mol&lt;sup&gt;-1&lt;/sup&gt;) and presents a diurnal variation similar to that of
      DMS. SO&lt;sub&gt;2&lt;/sub&gt; levels ranged from 220 to 2970 pmol·mol&lt;sup&gt;-1&lt;/sup&gt; (mean value of
      1030 pmol·mol&lt;sup&gt;-1&lt;/sup&gt;), while nss-SO&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;2-&lt;/sup&gt; and MS&lt;sup&gt;-&lt;/sup&gt; ranged from 330 to
      7100 pmol·mol&lt;sup&gt;-1&lt;/sup&gt;, (mean value of 1440 pmol·mol&lt;sup&gt;-1&lt;/sup&gt;) and 1.1 to
      37.5 pmol·mol&lt;sup&gt;-1&lt;/sup&gt; (mean value of 11.5 pmol·mol&lt;sup&gt;-1&lt;/sup&gt;) respectively.&lt;br&gt;
      &lt;br&gt;
      Of particular interest are the measurements of gaseous MSA and H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt;. MSA ranged
      from below the detection limit (3x10&lt;sup&gt;4&lt;/sup&gt;) to 3.7x10&lt;sup&gt;7&lt;/sup&gt;
      molecules cm&lt;sup&gt;-3&lt;/sup&gt;, whereas H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt; ranged between
      1x10&lt;sup&gt;5&lt;/sup&gt; and 9.0x10&lt;sup&gt;7&lt;/sup&gt; molecules cm&lt;sup&gt;-3&lt;/sup&gt;. The measured
      H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt; maxima are among the highest reported in literature and can be attributed to high
      insolation, absence of precipitation and increased SO&lt;sub&gt;2&lt;/sub&gt; levels in the area. From the concurrent
      SO&lt;sub&gt;2&lt;/sub&gt;, OH, and H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt; measurements a sticking coefficient of
      0.52±0.28 was calculated for H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt;. From the concurrent MSA, OH, and DMS measurements the yield of gaseous MSA from
      the OH-initiated oxidation of DMS was calculated to range between
      0.1-0.4%. This low MSA yield implies that gaseous MSA levels can not account for the observed
      MS&lt;sup&gt;-&lt;/sup&gt; levels. Heterogeneous reactions of DMSO on aerosols should be considered to explain the
      observed levels of MS&lt;sup&gt;-&lt;/sup&gt;.</p>
</abstract>
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