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<article language="en">
	<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>8</volume_number>
		<issue_number>4</issue_number>
		<publication_year>2008</publication_year>
	</journal>
	<doi>10.5194/acpd-8-16291-2008</doi>
	<article_url>http://www.atmos-chem-phys-discuss.net/8/16291/2008/</article_url>
	<abstract_html>http://www.atmos-chem-phys-discuss.net/8/16291/2008/acpd-8-16291-2008.html</abstract_html>
	<fulltext_pdf>http://www.atmos-chem-phys-discuss.net/8/16291/2008/acpd-8-16291-2008.pdf</fulltext_pdf>
	<start_page>16291</start_page>
	<end_page>16333</end_page>
	<publication_date>2008-08-26</publication_date>
	<article_title content_type="html">Uncertainty in global CCN concentrations from uncertain aerosol nucleation and primary emission rates</article_title>
	<authors>
		<author numeration="1" affiliations="1,2">
			<name>J. R. Pierce</name>
			<email>jeffrey.robert.pierce@gmail.com</email>
		</author>
		<author numeration="2" affiliations="1">
			<name>P. J. Adams</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Center for Atmospheric Particle Studies, Carnegie Mellon Univ., Pittsburgh, PA, USA</affiliation>
		<affiliation numeration="2" content_type="html">now at: Goddard Space Flight Center, Greenbelt, MD, USA, 20771, USA</affiliation>
	</affiliations>
	<abstract content_type="html">The indirect effect of aerosols on climate is highly uncertain and limits
our ability to assess anthropogenic climate change. The foundation of this
uncertainty is uncertainty in the number of cloud condensation nuclei (CCN),
which itself stems from uncertainty in aerosol nucleation, primary emission
and growth rates. In this paper, we use a global general circulation model
with aerosol microphysics to assess how the uncertainties in aerosol
nucleation, emission and growth rates affect our prediction of CCN(0.2%)
concentrations. Using two nucleation rate parameterizations that differ in
globally averaged nucleation rate by 10&lt;sup&gt;6&lt;/sup&gt;, the tropospheric average
CCN(0.2%) concentrations vary by 17% and the boundary layer average
vary by 12%. This sensitivity of tropospheric average CCN(0.2%) to the
nucleation parameterizations increases to 33% and 20% when the total
primary emissions are reduced by a factor of 3 and the SOA condensation
rates are increased by a factor of 3.5, respectively. These results show
that it is necessary to understand better global nucleation rates when
determining CCN concentrations. When primary emissions rates are varied by a
factor of 3 while using the slower nucleation rate parameterization,
tropospheric average CCN(0.2%) concentrations also vary by 17%, but
boundary layer average vary by 40%. Using the faster nucleation rate
parameterization, these changes drop to 3% and 22%, respectively.
These results show the importance of reducing uncertainties in primary
emissions, which appear from these results to be somewhat more important for
CCN than the much larger uncertainties in nucleation. These results also
show that uncertainties in nucleation and primary emissions are more
important when sufficient condensable material is available to grow them to
CCN sizes. The percent change in CCN(0.2%) concentration between
pre-industrial times and present day does not depend greatly on the
nucleation rate parameterization used for our base case scenarios; however,
because other factors, such as primary emissions and SOA, are uncertain in
both time periods, this may be a coincidence.</abstract>
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</article>

