Audrė Kalinauskaitė

Urban science plays a pivotal role in understanding the complex interactions between fireworks, air quality, and urban environments. Dense firework smoke worsens air quality and poses a health hazard to the public. In this study, we show a situation where extremely foggy meteorological conditions coincided with intense anthropogenic emissions, including fireworks, in an urban area. For the first time, the chemical composition and sources of non-refractory submicron aerosol (NR-PM₁) in outdoor and indoor air were characterized in Vilnius (Lithuania) using an aerosol chemical speciation monitor (ACSM) and Positive Matrix Factorization for the period before the fireworks, on New Year’s Eve, and after the fireworks in 2020/2021; thus, typical changes were assessed. Due to stagnant weather conditions and increased traffic, the highest concentrations of black carbon (BC) (13.8 μg/m³) were observed before the fireworks display. The contribution of organic (Org) fraction to the total NR-PM₁ mass concentration, in the comparison of the values of a typical night and New Year’s Eve (from 9 p.m. to 6 a.m.), increased from 43% to 70% and from 47% to 60% in outdoor and indoor air, respectively. Biomass-burning organic aerosol (BBOA, 48% (44%)) and hydrocarbon-like organic aerosol (HOA, 35% (21%)) dominated the organic fraction indoors and outdoors, respectively. HOA was likely linked to increased traffic during the event, while BBOA may have been related to domestic heating and fireworks.

The present study investigated the characteristics of carbonaceous species in an urban background site. Real-time measurements of inorganic (sulfate, nitrate, ammonium, chloride, and black carbon [BC]) and organic submicron aerosols (OA) were carried out at the urban background site of Vilnius, Lithuania, during January–February 2014. An aerosol chemical speciation monitor (ACSM, Aerodyne Research Inc., Billerica, MA, USA) and co-located 7-λ aethalometer (AE-31, Magee Scientific, Berkeley, CA, USA) were used to analyze the chemical compositions, sources, and extinction characteristics of the PM₁. Extremely contrasting meteorological conditions were observed during the studied period due to the transition from moderately cold (~2 °C) conditions to extremely cold conditions with a lowest temperature of −25 °C; therefore, three investigation episodes were considered. The identified periods corresponded to the transition time from the moderately cold to the extremely cold winter period, which was traced by the change in the average temperature for the study days of 1–13 January, with T = −5 °C and RH = 92%, in contrast to the period of 14–31 January, with T = −14 °C and RH = 74%, and the very short third period of 1–3 February, with T = −8 °C and RH = 35%. On average, organics accounted for the major part (53%) of the non-refractory submicron aerosols (NR-PM₁), followed by nitrate (18%) and sulfate (9%). The source apportionment results showed the five most common OA components, such as traffic and heating, to be related to hydrocarbon-like organic aerosols (HOA_traffic and HOA_heating, respectively), biomass-burning organic aerosols (BBOA), local organic aerosol (LOA), and secondary organic aerosol (SOA). Traffic emissions contributed 53% and biomass burning 47% to the BC concentration level. The highest BC and OA concentrations were, on average, associated with air masses originating from the southwest and east–southeast. Furthermore, the results of the PSCF and CWT methods indicated the main source regions that contributed the most to the BC concentration in Vilnius to be the following: central–southwestern and northeastern Poland, northwestern–southwestern and eastern Belarus, northwestern Ukraine, and western Russia. However, the potential sources of OA were widely distributed.