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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-6-1435-2006</article-id>
<title-group>
<article-title>Concentrations of OH and HO&lt;sub&gt;2&lt;/sub&gt; radicals during NAMBLEX: measurements and steady state analysis</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Smith</surname>
<given-names>S. C.</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>Lee</surname>
<given-names>J. D.</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>Bloss</surname>
<given-names>W. J.</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>Johnson</surname>
<given-names>G. P.</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>Ingham</surname>
<given-names>T.</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>Heard</surname>
<given-names>D. E.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>School of Chemistry, University of Leeds, Leeds, LS2 9JT, UK</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>Department of Chemistry, University of York, Heslington, York, YO10 5DD, UK</addr-line>
</aff>
<pub-date pub-type="epub">
<day>04</day>
<month>05</month>
<year>2006</year>
</pub-date>
<volume>6</volume>
<issue>5</issue>
<fpage>1435</fpage>
<lpage>1453</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/6/1435/2006/acp-6-1435-2006.html">This article is available from http://www.atmos-chem-phys.net/6/1435/2006/acp-6-1435-2006.html</self-uri>
<self-uri xlink:href="http://www.atmos-chem-phys.net/6/1435/2006/acp-6-1435-2006.pdf">The full text article is available as a PDF file from http://www.atmos-chem-phys.net/6/1435/2006/acp-6-1435-2006.pdf</self-uri>
<abstract>
<p>OH and HO&lt;sub&gt;2&lt;/sub&gt; concentrations were measured simultaneously at
the Mace Head Atmospheric Research Station in the summer of 2002
during the NAMBLEX (North Atlantic Marine Boundary Layer EXperiment)
field campaign. OH was measured by laser-induced fluorescence
employing the FAGE (Fluorescence Assay by Gas Expansion) technique,
with a mean daytime detection limit of 2.7&amp;times;10&lt;sup&gt;5&lt;/sup&gt; molecule cm&lt;sup&gt;&amp;minus;3&lt;/sup&gt;
(5 min acquisition period; signal-to-noise
ratio = 1). HO&lt;sub&gt;2&lt;/sub&gt; was detected as OH following its chemical
conversion through addition of NO, with a mean detection limit of
4.4&amp;times;10&lt;sup&gt;6&lt;/sup&gt; molecule cm&lt;sup&gt;&amp;minus;3&lt;/sup&gt;. The diurnal variation of OH was
measured on 24 days, and that of HO&lt;sub&gt;2&lt;/sub&gt; on 17 days. The local
solar noon OH concentrations ranged between (3&amp;ndash;8)&amp;times;10&lt;sup&gt;6&lt;/sup&gt; molecule 
cm&lt;sup&gt;&amp;minus;3&lt;/sup&gt;, with a 24 h mean concentration of
9.1&amp;times;10&lt;sup&gt;5&lt;/sup&gt; molecule cm&lt;sup&gt;&amp;minus;3&lt;/sup&gt;. The local solar noon
HO&lt;sub&gt;2&lt;/sub&gt; concentrations were (0.9&amp;ndash;2.1)&amp;times;10&lt;sup&gt;8&lt;/sup&gt;  molecule
 cm&lt;sup&gt;&amp;minus;3&lt;/sup&gt; (3.5&amp;ndash;8.2 pptv), with a 24 h mean concentration of 4.2&amp;times;10&lt;sup&gt;7&lt;/sup&gt; molecule
 cm&lt;sup&gt;&amp;minus;3&lt;/sup&gt; (1.6 pptv). HO&lt;sub&gt;2&lt;/sub&gt; radicals in the
range (2&amp;ndash;3)&amp;times;10&lt;sup&gt;7&lt;/sup&gt; molecule cm&lt;sup&gt;&amp;minus;3&lt;/sup&gt; were observed at
night. During NAMBLEX, a comprehensive suite of supporting
measurements enabled a detailed study of the behaviour of HO&lt;sub&gt;x&lt;/sub&gt;
radicals under primarily clean marine conditions. Steady state expressions are used to calculate OH and
HO&lt;sub&gt;2&lt;/sub&gt; concentrations and to evaluate the effect of different
free-radical sources and sinks. The diurnally averaged calculated to
measured OH ratio was 1.04&amp;plusmn;0.36, but the ratio displays a
distinct diurnal variation, being less than 1 during the early
morning and late afternoon/evening, and greater than 1 in the middle
of the day. For HO&lt;sub&gt;2&lt;/sub&gt; there was an overprediction, with the
agreement between calculated and measured concentrations improved by
including reaction with measured IO and BrO radicals and uptake to
aerosols. Increasing the concentration of IO radicals included in
the calculations to above that measured by a DOAS instrument with an
absorption path located mainly over the ocean, reflecting the domination
of the inter-tidal region as an iodine source at Mace Head, led to
further improvement. The results are compared with previous
measurements at Mace Head, and elsewhere in the remote marine
boundary layer.</p>
</abstract>
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