ACTRIS ACSM intercomparison – Part 2: Intercomparison of ME-2 organic source apportionment results from 15 individual, co-located aerosol mass spectrometers-Reference-Cited by-同舟云学术

ACTRIS ACSM intercomparison – Part 2: Intercomparison of ME-2 organic source apportionment results from 15 individual, co-located aerosol mass spectrometers

Published:2015-02-04 Issue: Volume: Page:
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Fröhlich R.,Crenn V.,Setyan A.,Belis C. A.,Canonaco F.,Favez O.,Riffault V.^ORCID,Slowik J. G.,Aas W.,Aijälä M.,Alastuey A.^ORCID,Artiñano B.,Bonnaire N.,Bozzetti C.,Bressi M.,Carbone C.,Coz E.^ORCID,Croteau P. L.,Cubison M. J.,Esser-Gietl J. K.,Green D. C.,Gros V.,Heikkinen L.,Herrmann H.,Jayne J. T.,Lunder C. R.,Minguillón M. C.^ORCID,Močnik G.^ORCID,O'Dowd C. D.,Ovadnevaite J.,Petralia E.,Poulain L.^ORCID,Priestman M.,Ripoll A.,Sarda-Estève R.,Wiedensohler A.,Baltensperger U.,Sciare J.,Prévôt A. S. H.

Abstract

Abstract. Chemically resolved atmospheric aerosol data sets from the largest intercomparison of the Aerodyne aerosol chemical speciation monitors (ACSM) performed to date were collected at the French atmospheric supersite SIRTA. In total 13 quadrupole ACSMs (Q-ACSM) from the European ACTRIS ACSM network, one time-of-flight ACSM (ToF-ACSM), and one high-resolution ToF aerosol mass spectrometer (AMS) were operated in parallel for about three weeks in November and December 2013. Part 1 of this study reports on the accuracy and precision of the instruments for all the measured species. In this work we report on the intercomparison of organic components and the results from factor analysis source apportionment by positive matrix factorisation (PMF) utilising the multilinear engine 2 (ME-2). Except for the organic contribution of m/z 44 to the total organics (f44), which varied by factors between 0.6 and 1.3 compared to the mean, the peaks in the organic mass spectra were similar among instruments. The m/z 44 differences in the spectra resulted in a variable f44 in the source profiles extracted by ME-2, but had only a minor influence on the extracted mass contributions of the sources. The presented source apportionment yielded four factors for all 15 instruments: hydrocarbon-like organic aerosol (HOA), cooking-related organic aerosol (COA), biomass burning-related organic aerosol (BBOA) and secondary oxygenated organic aerosol (OOA). Individual application and optimisation of the ME-2 boundary conditions (profile constraints) are discussed together with the investigation of the influence of alternative anchors (reference profiles). A comparison of the ME-2 source apportionment output of all 15 instruments resulted in relative SD from the mean between 13.7 and 22.7% of the source's average mass contribution depending on the factors (HOA: 14.3 ± 2.2%, COA: 15.0 ± 3.4%, OOA: 41.5 ± 5.7%, BBOA: 29.3 ± 5.0%). Factors which tend to be subject to minor factor mixing (in this case COA) have higher relative uncertainties than factors which are recognised more readily like the OOA. Averaged over all factors and instruments the relative first SD from the mean of a source extracted with ME-2 was 17.2%.

Funder

Seventh Framework Programme

Agence de l'Environnement et de la Maîtrise de l'Energie

Publisher

Copernicus GmbH

Link

https://amt.copernicus.org/preprints/8/1559/2015/amtd-8-1559-2015.pdf

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