Comment on acp-2022-467

Abstract

Urban air consists of a complex mixture of gaseous and particulate species from anthropogenic and biogenic sources that are further processed in the atmosphere. This study investigated the features and sources of volatile organic compounds (VOCs) and submicron organic aerosol (OA) at a street canyon in Helsinki, Finland in late summer. The main anthropogenic VOCs (aVOCs) and biogenic VOCs (bVOCs) were analyzed with an online gas chromatograph mass spectrometer, whereas the composition and size distribution of submicron particles was measured with a soot particle aerosol mass spectrometer. This study showed that aVOC concentrations were significantly higher than bVOC concentrations at the street canyon. The largest aVOC concentrations were measured for toluene (campaign-average 1630 ng m-3) and p/m xylene (campaign-average 1070 ng m-3), while the dominating bVOCs was α-pinene (campaign-average 200 ng m-3). The special focus of this research was also on the oxidation of VOCs and the association between VOCs and OA in ambient air. Production rates of the oxidized compounds (OxPR) from the VOC reactions revealed that the main local sources of the oxidation products were O3 oxidation of bVOCs (66 % of total OxPR) and OH radical oxidation of aVOCs and bVOCs (25 % of total OxPR). Overall, aVOCs produced much smaller portion of the oxidation products (18 %) than bVOCs (82 %). For particle phase organics, the source apportionment analysis extracted six factors for OA. Three OA factors were related to primary OA sources, traffic (24 % of OA, two OA types) and coffee roastery (7 % of OA), whereas the largest fraction of OA (69 %) consisted of oxygenated OA (OOA). OOA was divided into less oxidized semi-volatile OA (SV-OOA; 40 % of OA) and two types of low-volatility OA (LV-OOA; 30 %). SV-OOA was likely to originate from biogenic sources since it correlated with an oxidation product of monoterpene, nopinone. LV-OOA consisted of highly oxygenated long-range or regionally transported OA that had no correlation with local oxidant concentrations as it had already spent several days in the atmosphere before reaching the measurement site. By investigating specific air quality cases, it was noticed that the influence of main pollutant sources was different for VOCs and OA at the street canyon. Vehicle emissions impacted both VOC and OA concentrations, whereas the influence of biogenic emissions was more clearly detected in the VOC concentrations than in OA due to the specific VOCs attributed to biogenic emissions. In contrast, the emissions from the local coffee roastery had a distinctive mass spectrum for OA but they could not be seen in the VOC measurements due to the measurement limitations for the large VOC compounds. Long-range transport increased the OA concentrations and oxidation state considerably, while its effect was observed less clearly in the VOC measurements due to the oxidation of most VOC in the atmosphere during the transport. Overall, this study revealed that in order to properly characterize the impact of different emission sources to air quality, health and climate, it is of importance to describe both gaseous and particulate emissions and understand how they interact as well as their phase transfers in the atmosphere during the aging process.