Chemical characterization of submicron regional background aerosols in the western Mediterranean using an Aerosol Chemical Speciation Monitor. Minguillón, M., C., Ripoll, a., Pérez, N., Prévôt, a., S., H., Canonaco, F., Querol, X., & Alastuey, a. Atmospheric Chemistry and Physics, 15(11):6379-6391, 2015.
Chemical characterization of submicron regional background aerosols in the western Mediterranean using an Aerosol Chemical Speciation Monitor [pdf]Paper  Chemical characterization of submicron regional background aerosols in the western Mediterranean using an Aerosol Chemical Speciation Monitor [link]Website  abstract   bibtex   

An Aerosol Chemical Speciation Monitor (ACSM, Aerodyne Research Inc.) was deployed at the Montseny (MSY; 41° 46'46" N, 02° 21'29" E, 720 m a.s.l.) regional background site in the western Mediterranean, Spain, from June 2012 to July 2013 to measure real-time inorganic (nitrate, sulfate, ammonium and chloride) and organic submicron aerosol concentrations. Co-located measurements, including real-time submicron particulate matter (PM1) and black carbon (BC) concentrations, and off-line PM1 chemical analysis were also carried out. This is one of the few studies that compare ACSM data with off-line PM1 measurements, avoiding the tail of the coarse mode included in the PM2.5 fraction. The ACSM + BC concentrations agreed with the PM1 measurements, and a strong correlation was found between the concentrations of ACSM species and the off-line measurements, although some discrepancies remain unexplained. Results point to a current underestimation of the relative ionization efficiency (RIE) established for organic aerosol (OA), which should be revised in the future. The OA was the major component of submicron aerosol (53% of PM1), with a higher contribution in summer (58% of PM1) than in winter (45% of PM1). Source apportionment of OA was carried out by applying positive matrix factorization (PMF), using the multilinear engine (ME-2) to the organic mass spectral data matrix. Three sources were identified in summer: hydrocarbon-like OA (HOA), low-volatile oxygenated OA (LV-OOA), and semi-volatile oxygenated OA (SV-OOA). The secondary OA (SOA; 4.8 μg m−3, sum of LV-OOA and SV-OOA) accounted for 85% of the total OA, and its formation during daytime (mainly SV-OOA) was estimated to be 1.1 μg m−3. In winter, HOA was also identified (12% of OA), a contribution from biomass burning OA (BBOA) was included and it was not possible to differentiate between two different SOA factors, but a single oxygenated OA (OOA) factor was resolved. The OOA contribution represented 60% of the total OA, with a degree of oxidation higher than both OOA summer factors. An intense wildfire episode was studied, obtaining a region-specific BBOA profile.


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