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<article language="en">
	<journal>
		<journal_title>Atmospheric Measurement Techniques Discussions</journal_title>
		<journal_url>www.atmos-meas-tech-discuss.net</journal_url>
		<eissn>1867-8610</eissn>
		<volume_number>2</volume_number>
		<issue_number>4</issue_number>
		<publication_year>2009</publication_year>
	</journal>
	<doi>10.5194/amtd-2-1783-2009</doi>
	<article_url>http://www.atmos-meas-tech-discuss.net/2/1783/2009/</article_url>
	<abstract_html>http://www.atmos-meas-tech-discuss.net/2/1783/2009/amtd-2-1783-2009.html</abstract_html>
	<fulltext_pdf>http://www.atmos-meas-tech-discuss.net/2/1783/2009/amtd-2-1783-2009.pdf</fulltext_pdf>
	<start_page>1783</start_page>
	<end_page>1835</end_page>
	<publication_date>2009-08-04</publication_date>
	<article_title content_type="html">Field inter-comparison of eleven atmospheric ammonia measurement techniques</article_title>
	<authors>
		<author numeration="1" affiliations="1,2">
			<name>K. von Bobrutzki</name>
		</author>
		<author numeration="2" affiliations="1">
			<name>C. F. Braban</name>
		</author>
		<author numeration="3" affiliations="1">
			<name>D. Famulari</name>
		</author>
		<author numeration="4" affiliations="1">
			<name>S. K. Jones</name>
		</author>
		<author numeration="5" affiliations="3">
			<name>T. Blackall</name>
		</author>
		<author numeration="6" affiliations="3">
			<name>T. E. L. Smith</name>
		</author>
		<author numeration="7" affiliations="4">
			<name>M. Blom</name>
		</author>
		<author numeration="8" affiliations="5">
			<name>H. Coe</name>
		</author>
		<author numeration="9" affiliations="5">
			<name>M. Gallagher</name>
		</author>
		<author numeration="10" affiliations="5">
			<name>M. Ghalaieny</name>
		</author>
		<author numeration="11" affiliations="5">
			<name>M. R. McGillen</name>
		</author>
		<author numeration="12" affiliations="5">
			<name>C. J. Percival</name>
		</author>
		<author numeration="13" affiliations="5">
			<name>J. D. Whitehead</name>
		</author>
		<author numeration="14" affiliations="6">
			<name>R. Ellis</name>
		</author>
		<author numeration="15" affiliations="6">
			<name>J. Murphy</name>
		</author>
		<author numeration="16" affiliations="7">
			<name>A. Mohacsi</name>
		</author>
		<author numeration="17" affiliations="9">
			<name>H. Junninen</name>
		</author>
		<author numeration="18" affiliations="8">
			<name>A. Pogany</name>
		</author>
		<author numeration="19" affiliations="9">
			<name>S. Rantanen</name>
		</author>
		<author numeration="20" affiliations="1">
			<name>M. A. Sutton</name>
		</author>
		<author numeration="21" affiliations="1">
			<name>E. Nemitz</name>
		</author>
	</authors>
	<affiliations>
		<affiliation numeration="1" content_type="html">Centre for Ecology &amp; Hydrology, Edinburgh, UK</affiliation>
		<affiliation numeration="2" content_type="html">Leibniz-Institute for Agricultural Engineering, Potsdam, Germany</affiliation>
		<affiliation numeration="3" content_type="html">Department of Geography, King&apos;s College London, London, UK</affiliation>
		<affiliation numeration="4" content_type="html">Energy Research Foundation of the Netherlands, Petten, The Netherlands</affiliation>
		<affiliation numeration="5" content_type="html">School of Earth, Atmospheric and Environmental Science, University of Manchester, Manchester, UK</affiliation>
		<affiliation numeration="6" content_type="html">Department of Physics, University of Toronto, Toronto, Canada</affiliation>
		<affiliation numeration="7" content_type="html">Research Group on Laser Physics of the Hungarian Academy of Sciences, Budapest, Hungary</affiliation>
		<affiliation numeration="8" content_type="html">Department of Optics and Quantum Electronics, University of Szeged, Szeged, Hungary</affiliation>
		<affiliation numeration="9" content_type="html">Department of Physics, University of Helsinki, Helsinki, Finland</affiliation>
	</affiliations>
	<abstract content_type="html">Eleven instruments for the measurement of ambient concentrations of
atmospheric ammonia gas (NH&lt;sub&gt;3&lt;/sub&gt;), based on eight different measurement
methods were inter-compared above an intensively managed agricultural field
in late summer 2008 in S. Scotland. To test the instruments over a wide range
of concentrations, the field was fertilised with urea midway through the
experiment, leading to an increase in the average concentration from 10 to
100 ppbv. The instruments deployed included three wet-chemistry systems, one
with offline analysis (annular rotating batch denuder, RBD) and two with
online-analysis (Annular Denuder sampling with online Analysis, AMANDA;
AiRRmonia), two Quantum Cascade Laser Absorption Spectrometers (a large-cell
dual system, DUAL-QCLAS, and a compact system, c-QCLAS), two photo-acoustic
spectrometers (WaSul-Flux, Nitrolux-100), a Cavity Ring Down Spectrosmeter
(CRDS), a Chemical Ionisation Mass Spectrometer (CIMS), an ion mobility
spectrometer (IMS) and an Open-Path Fourier Transform Infra-Red (OP-FTIR)
spectroscopy. Each instrument was compared with each other and with the
average concentration of all instruments. An overall good agreement of hourly
average concentrations between the instruments (&lt;i&gt;R&lt;/i&gt;&lt;sup&gt;2&lt;/sup&gt;&gt;0.84), was observed
for NH&lt;sub&gt;3&lt;/sub&gt; concentrations at the field of up to 120 ppbv with the slopes
against the average ranging from 0.67 (DUAL-QCLAS) to 1.13 (AiRRmonia) with
intercepts of –0.74 ppbv (RBD) to +2.69 ppbv (CIMS). More variability was
found for performance for lower concentrations (&amp;lt;10 ppbv). Here the
overruling factors affecting measurement precision are (a) the inlet design,
(b) the state of inlet filters (where applicable), and (c) the quality of
gas-phase standards (where applicable). By reference to the fast (1 Hz)
instruments deployed during the study, it was possible to characterize the
response times of the slower instruments.</abstract>
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</article>

