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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-12-10759-2012</article-id>
<title-group>
<article-title>Atmospheric removal times of the aerosol-bound radionuclides &lt;sup&gt;137&lt;/sup&gt;Cs and &lt;sup&gt;131&lt;/sup&gt;I measured after the Fukushima Dai-ichi nuclear accident &amp;ndash; a constraint for air quality and climate models</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kristiansen</surname>
<given-names>N. I.</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>Stohl</surname>
<given-names>A.</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>Wotawa</surname>
<given-names>G.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
</contrib-group><aff id="aff1">
<label>1</label>
<addr-line>Norwegian Institute for Air Research (NILU), Kjeller, Norway</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>Central Institute for Meteorology and Geodynamics, Vienna, Austria</addr-line>
</aff>
<pub-date pub-type="epub">
<day>16</day>
<month>11</month>
<year>2012</year>
</pub-date>
<volume>12</volume>
<issue>22</issue>
<fpage>10759</fpage>
<lpage>10769</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>
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<self-uri xlink:href="http://www.atmos-chem-phys.net/12/10759/2012/acp-12-10759-2012.pdf">The full text article is available as a PDF file from http://www.atmos-chem-phys.net/12/10759/2012/acp-12-10759-2012.pdf</self-uri>
<abstract>
<p>Caesium-137 (&lt;sup&gt;137&lt;/sup&gt;Cs) and iodine-131 (&lt;sup&gt;131&lt;/sup&gt;I) are radionuclides of
particular concern during nuclear accidents, because they are emitted in
large amounts and are of significant health impact. &lt;sup&gt;137&lt;/sup&gt;Cs and &lt;sup&gt;131&lt;/sup&gt;I
attach to the ambient accumulation-mode (AM) aerosols and share their fate as
the aerosols are removed from the atmosphere by scavenging within clouds,
precipitation and dry deposition. Here, we estimate their removal times from
the atmosphere using a unique high-precision global measurement data set
collected over several months after the accident at the Fukushima Dai-ichi
nuclear power plant in March 2011. The noble gas xenon-133 (&lt;sup&gt;133&lt;/sup&gt;Xe), also
released during the accident, served as a passive tracer of air mass
transport for determining the removal times of &lt;sup&gt;137&lt;/sup&gt;Cs and &lt;sup&gt;131&lt;/sup&gt;I via
the decrease in the measured ratios &lt;sup&gt;137&lt;/sup&gt;Cs/&lt;sup&gt;133&lt;/sup&gt;Xe and
&lt;sup&gt;131&lt;/sup&gt;I/&lt;sup&gt;133&lt;/sup&gt;Xe over time. After correction for radioactive decay, the
&lt;sup&gt;137&lt;/sup&gt;Cs/&lt;sup&gt;133&lt;/sup&gt;Xe ratios reflect the removal of aerosols by wet and dry
deposition, whereas the &lt;sup&gt;131&lt;/sup&gt;I/&lt;sup&gt;133&lt;/sup&gt;Xe ratios are also influenced by
aerosol production from gaseous &lt;sup&gt;131&lt;/sup&gt;I. We find removal times for
&lt;sup&gt;137&lt;/sup&gt;Cs of 10.0–13.9 days and for &lt;sup&gt;131&lt;/sup&gt;I of 17.1–24.2 days during
April and May 2011. The removal time of &lt;sup&gt;131&lt;/sup&gt;I is longer due to the
aerosol production from gaseous &lt;sup&gt;131&lt;/sup&gt;I, thus the removal time for
&lt;sup&gt;137&lt;/sup&gt;Cs serves as a better estimate for aerosol lifetime. The removal time
of &lt;sup&gt;131&lt;/sup&gt;I is of interest for semi-volatile species. We discuss possible
caveats (e.g. late emissions, resuspension) that can affect the results, and
compare the &lt;sup&gt;137&lt;/sup&gt;Cs removal times with observation-based and modeled
aerosol lifetimes. Our &lt;sup&gt;137&lt;/sup&gt;Cs removal time of 10.0&amp;ndash;13.9 days should be
representative of a &quot;background&quot; AM aerosol well mixed in the extratropical
Northern Hemisphere troposphere. It is expected that the lifetime of this
vertically mixed background aerosol is longer than the lifetime of fresh AM
aerosols directly emitted from surface sources. However, the substantial
difference to the mean lifetimes of AM aerosols obtained from aerosol models,
typically in the range of 3–7 days, warrants further research on the cause of
this discrepancy. Too short modeled AM aerosol lifetimes would have serious
implications for air quality and climate model predictions.</p>
</abstract>
<counts><page-count count="11"/></counts>
</article-meta>
</front>
<body/>
<back>
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