Seasonal differences in oxygenated organic aerosol composition: implications for emissions sources and factor analysis

Aerosol chemical speciation monitor (ACSM) measurements were performed in Zurich, Switzerland, for 13 months (February 2011 through February 2012). Many previous studies using this or related instruments have utilized the fraction of organic mass measured at <i>m/z</i> 44 (<i>f<...

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Main Authors: F. Canonaco, J. G. Slowik, U. Baltensperger, A. S. H. Prévôt
Format: Article
Language:English
Published: Copernicus Publications 2015-06-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/15/6993/2015/acp-15-6993-2015.pdf
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spelling doaj-2bca1d3777f84f7ab5d0064d218d440e2020-11-24T23:15:17ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242015-06-0115126993700210.5194/acp-15-6993-2015Seasonal differences in oxygenated organic aerosol composition: implications for emissions sources and factor analysisF. Canonaco0J. G. Slowik1U. Baltensperger2A. S. H. Prévôt3Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, 5232 Villigen PSI, SwitzerlandLaboratory of Atmospheric Chemistry, Paul Scherrer Institute, 5232 Villigen PSI, SwitzerlandLaboratory of Atmospheric Chemistry, Paul Scherrer Institute, 5232 Villigen PSI, SwitzerlandLaboratory of Atmospheric Chemistry, Paul Scherrer Institute, 5232 Villigen PSI, SwitzerlandAerosol chemical speciation monitor (ACSM) measurements were performed in Zurich, Switzerland, for 13 months (February 2011 through February 2012). Many previous studies using this or related instruments have utilized the fraction of organic mass measured at <i>m/z</i> 44 (<i>f</i><sub>44</sub>), which is typically dominated by the CO<sub>2</sub><sup>+</sup> ion and related to oxygenation, as an indicator of atmospheric aging. The current study demonstrates that during summer afternoons, when photochemical processes are most vigorous as indicated by high oxidant – OX (O<sub>3</sub> + NO<sub>2</sub>), <i>f</i><sub>44</sub> for ambient secondary organic aerosol (SOA) is not higher but is rather similar or lower than on days with low OX. On the other hand, <i>f</i><sub>43</sub> (less oxidized fragment) tends to increase. These changes are discussed in the <i>f</i><sub>44</sub> / <i>f</i><sub>43</sub> space frequently used to interpret ACSM and aerosol mass spectrometer (AMS) data. This is likely due to the formation of semi-volatile oxygenated aerosol produced from biogenic precursor gases, whose emissions increase with ambient temperature. <br><br> In addition, source apportionment analyses conducted on winter and summer data using positive matrix factorization (PMF) yield semi-volatile oxygenated organic aerosol (SV-OOA) factors that retain source-related chemical information. Winter SV-OOA is highly influenced by biomass burning, whereas summer SV-OOA is to a high degree produced from biogenic precursor gases. These sources contribute to substantial differences between the winter and summer <i>f</i><sub>44</sub> / <i>f</i><sub>43</sub> data, suggesting that PMF analysis of multi-season data employing only two OOA factors cannot capture the seasonal variability of OOA.http://www.atmos-chem-phys.net/15/6993/2015/acp-15-6993-2015.pdf
collection DOAJ
language English
format Article
sources DOAJ
author F. Canonaco
J. G. Slowik
U. Baltensperger
A. S. H. Prévôt
spellingShingle F. Canonaco
J. G. Slowik
U. Baltensperger
A. S. H. Prévôt
Seasonal differences in oxygenated organic aerosol composition: implications for emissions sources and factor analysis
Atmospheric Chemistry and Physics
author_facet F. Canonaco
J. G. Slowik
U. Baltensperger
A. S. H. Prévôt
author_sort F. Canonaco
title Seasonal differences in oxygenated organic aerosol composition: implications for emissions sources and factor analysis
title_short Seasonal differences in oxygenated organic aerosol composition: implications for emissions sources and factor analysis
title_full Seasonal differences in oxygenated organic aerosol composition: implications for emissions sources and factor analysis
title_fullStr Seasonal differences in oxygenated organic aerosol composition: implications for emissions sources and factor analysis
title_full_unstemmed Seasonal differences in oxygenated organic aerosol composition: implications for emissions sources and factor analysis
title_sort seasonal differences in oxygenated organic aerosol composition: implications for emissions sources and factor analysis
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2015-06-01
description Aerosol chemical speciation monitor (ACSM) measurements were performed in Zurich, Switzerland, for 13 months (February 2011 through February 2012). Many previous studies using this or related instruments have utilized the fraction of organic mass measured at <i>m/z</i> 44 (<i>f</i><sub>44</sub>), which is typically dominated by the CO<sub>2</sub><sup>+</sup> ion and related to oxygenation, as an indicator of atmospheric aging. The current study demonstrates that during summer afternoons, when photochemical processes are most vigorous as indicated by high oxidant – OX (O<sub>3</sub> + NO<sub>2</sub>), <i>f</i><sub>44</sub> for ambient secondary organic aerosol (SOA) is not higher but is rather similar or lower than on days with low OX. On the other hand, <i>f</i><sub>43</sub> (less oxidized fragment) tends to increase. These changes are discussed in the <i>f</i><sub>44</sub> / <i>f</i><sub>43</sub> space frequently used to interpret ACSM and aerosol mass spectrometer (AMS) data. This is likely due to the formation of semi-volatile oxygenated aerosol produced from biogenic precursor gases, whose emissions increase with ambient temperature. <br><br> In addition, source apportionment analyses conducted on winter and summer data using positive matrix factorization (PMF) yield semi-volatile oxygenated organic aerosol (SV-OOA) factors that retain source-related chemical information. Winter SV-OOA is highly influenced by biomass burning, whereas summer SV-OOA is to a high degree produced from biogenic precursor gases. These sources contribute to substantial differences between the winter and summer <i>f</i><sub>44</sub> / <i>f</i><sub>43</sub> data, suggesting that PMF analysis of multi-season data employing only two OOA factors cannot capture the seasonal variability of OOA.
url http://www.atmos-chem-phys.net/15/6993/2015/acp-15-6993-2015.pdf
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