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A source-resolved three-dimensional chemical transport model, PMCAMx-SR (Particulate Matter Comprehensive Air-quality Model with extensions – Source Resolved), was applied in the continental US to investigate the contribution of the various components (primary and secondary) of biomass burning organic aerosol (bbOA) to organic aerosol levels. Two different schemes based on the volatility basis set were used for the simulation of the bbOA during different seasons. The first is the default scheme of PMCAMx-SR, and the second is a recently developed scheme based on laboratory experiments of the bbOA evolution. The simulations with the alternative bbOA scheme predict much higher total bbOA concentrations when compared with the base case ones. This is mainly due to the high emissions of intermediate-volatility organic compounds (IVOCs) assumed in the alternative scheme. The oxidation of these compounds is predicted to be a significant source of secondary organic aerosol. The impact of the other parameters that differ in the two schemes is low to negligible. The monthly average maximum predicted concentrations of the alternative bbOA scheme were approximately an order of magnitude higher than those of the default scheme during all seasons. The performance of the two schemes was evaluated against observed total organic aerosol concentrations from several measurement sites across the US. The results were different for the different seasons examined. The default scheme performed better during July and September, while the alternative scheme performed a little better during April. These results illustrate the uncertainty of the corresponding predictions and the need to quantify the emissions and reactions of IVOCs from specific biomass sources and to better constrain the total (primary and secondary) bbOA levels. [ABSTRACT FROM AUTHOR]

A source-resolved three-dimensional chemical transport model, PMCAMx-SR, was applied in the continental U.S. to investigate the contribution of the various components (primary and secondary) of biomass burning organic aerosol (bbOA) to organic aerosol levels. Two different schemes based on the volatility basis set were used for the simulation of the bbOA during different seasons. The first is the default scheme of PMCAMx-SR and the second is a recently developed scheme based on laboratory experiments of the bbOA evolution. The simulations with the alternative bbOA scheme predict much higher total bbOA concentrations when compared with the base case ones. This is mainly due to the high emissions of intermediate volatility organic compounds (IVOCs) assumed in the alternative scheme. The oxidation of these compounds is predicted to be a significant source of secondary organic aerosol. The impact of the other parameters that differ in the two schemes is low to negligible. The monthly average maximum predicted concentrations of the alternative bbOA scheme were approximately an order of magnitude higher than those of the default scheme during all seasons. The performance of the two schemes was evaluated against observed total organic aerosol concentrations from several measurement sites across the US. The results were mixed. The default scheme performed better during July and September while the alternative scheme performed a little better during April. These results illustrate the uncertainty of the corresponding predictions, the need to quantify the emissions and reactions of IVOCs from specific biomass sources, and to better constrain the total (primary and secondary) bbOA levels. [ABSTRACT FROM AUTHOR]

The chemical transport model PMCAMx was extended to investigate the effects of partitioning and photochemical aging of biomass burning emissions on organic aerosol (OA) concentrations. A source-resolved version of the model, PMCAMx-SR, was developed in which biomass burning emissions and their oxidation products are represented separately from the other OA components. The volatility distribution and chemical aging of biomass burning OA (BBOA) were simulated based on recent laboratory measurements. PMCAMx-SR was applied to Europe during an early summer period (1–29 May 2008) and a winter period (25 February–22 March 2009). During the early summer, the contribution of biomass burning (both primary and secondary species) to total OA levels over continental Europe was estimated to be approximately 16 %. During winter the contribution was nearly 47 %, due to both extensive residential wood combustion but also wildfires in Portugal and Spain. The intermediate volatility compounds (IVOCs) with effective saturation concentration values of 10 5 and 10 6 µ g m -3 are predicted to contribute around one third of the BBOA during the summer and 15 % during the winter by forming secondary OA (SOA). The uncertain emissions of these compounds and their SOA formation potential require additional attention. Evaluation of PMCAMx-SR predictions against aerosol mass spectrometer measurements in several sites around Europe suggests reasonably good performance for OA (fractional bias less than 35 % and fractional error less than 50 %). The performance was weaker during the winter suggesting uncertainties in residential heating emissions and the simulation of the resulting BBOA in this season. [ABSTRACT FROM AUTHOR]

The chemical transport model PMCAMx was extended to investigate the effects of partitioning and photochemical aging of biomass burning emissions on organic aerosol (OA) concentrations. A source-resolved version of the model, PMCAMx-SR, was developed in which biomass burning organic aerosol (bbOA) and its oxidation products are represented separately from the other OA components. The volatility distribution of bbOA and its chemical aging were simulated based on recent laboratory measurements. PMCAMx-SR was applied to Europe during an early summer (1–29 May 2008) and a winter period (25 February–22 March 2009). During the early summer, the contribution of biomass burning (both primary and secondary species) to total OA levels over continental Europe was estimated to be approximately 16%. During winter the same contribution was nearly 47% due to both extensive residential wood combustion, but also wildfires in Portugal and Spain. The intermediate volatility compounds (IVOCs) with effective saturation concentration values of 105 and 106μgm−3 are predicted to contribute around one third of the bbOA during the summer and 15% during the winter by forming secondary OA. The uncertain emissions of these compounds and their SOA formation potential require additional attention. Evaluation of PMCAMx-SR predictions against aerosol mass spectrometer measurements in several sites around Europe suggests reasonably good performance for OA (fractional bias less than 35% and fractional error less than 50%). The performance was weaker during the winter suggesting uncertainties in the residential heating emissions and the simulation of the resulting bbOA in this season. [ABSTRACT FROM AUTHOR]

Factor analysis of Aerosol Mass Spectrometer measurements (organic aerosol mass spectra) is often used to determine the sources of organic aerosol (OA). In this study we aim to gain insights regarding the ability of positive matrix factorization (PMF) to identify and quantify the OA sources accurately. We performed PMF and multilinear engine (ME-2) analysis on the predictions of a state-of-the-art chemical transport model (PMCAMx-SR) during a photochemically active period for specific sites in Europe in an effort to interpret the diverse factors usually identified by PMF analysis of field measurements. Our analysis used the predicted concentrations of 27 OA components, assuming that each of them is chemically different from the others. The PMF results based on the chemical transport model predictions are quite consistent (same number of factors and source types) with those of the analysis of AMS measurements. The estimated uncertainty of the contribution of fresh biomass burning is less than 30% and of the other primary sources less than 40%, when these sources contribute more than 20% to the total OA. For contributions between 10 and 20% the corresponding uncertainties increase to 50%. Finally, when these sources are small (less than 10% of the OA) the corresponding error is a factor of two or even three. One of the major questions in PMF analysis of AMS measurements concerns the sources of the two or more oxygenated OA (OOA) factors often reported in field studies. Our analysis suggests that these factors include secondary OA compounds from a variety of anthropogenic and biogenic sources and do not correspond to specific sources. Their characterization in the literature as low and high volatility factors is probably misleading, because they have overlapping volatility distributions. However, the average volatility of the one often characterized as low-volatility factor is indeed lower than that of the other (high volatility factor). Based on the analysis of the PMCAMx-SR predictions, the first oxygenated OA factor includes mainly highly-aged OA transported from outside Europe, but also highly aged secondary OA from precursors emitted in Europe. The second oxygenated OA factor contains fresher SOA from volatile, semi-volatile, and intermediate volatility anthropogenic and biogenic organic compounds. The exact contribution of these OA components to each OA factor depends on the site and the prevailing meteorology during the analysis period. [ABSTRACT FROM AUTHOR]