This study examines the influence of biomass burning on the organic content of urban aerosols in Zagreb, Croatia, by analyzing anhydrosugars, elemental carbon (EC), organic carbon (OC), and water-soluble organic carbon (WSOC) in PM_2.5 and PM₁ fractions collected during different seasons of 2022. Seasonal trends showed that the highest average concentrations of PM_2.5 (27 µg m⁻³) and PM₁ (17 µg m⁻³) were measured during the winter and decreased in the spring, summer, and autumn, which is in accordance with the specific activities and environmental conditions typical for each season. Different sources of OC and WSOC were noticed across different seasons; levoglucosan (LG) was measured during the winter (1314 ng m⁻³ in PM_2.5 and 931 ng m⁻³ in PM₁), indicating that biomass that was mostly used for residential heating was the main source rather than the agricultural activities that are usually common during warmer seasons. The contribution of LG to PM was 5.3%, while LG contributed to OC by up to 13.4% and LG contributed to WSOC by up to 36.5%. Deviations in typical seasonal variability of LG/WSOC revealed more intense biomass burning episodes during the autumn and several times during the winter season. A back trajectories HYSPLIT model revealed a long-range transport biomass emission source. The levoglucosan-to-mannosan (LG/MNS) ratios indicated the burning of mixed softwood and hardwood during colder seasons and the burning of softwood during warmer seasons. Spearman’s correlation tests and principal component analysis showed a strong and statistically significant (p < 0.05) correlation between LG, PM, OC, EC, and WSOC only during the winter season, demonstrating that they had the same origin in the winter, while their sources in other seasons were diverse.

This study aimed to investigate the effect of wildfire episodes on air quality in terms of particulate matter (PM) and carbonaceous compound concentration in ambient air, and to assess deviations from typical annual patterns. The sampling was performed at a rural background site near the Adriatic coast in Croatia through 2024. To better understand contributions caused by fire events, the levels of organic carbon (OC), elemental carbon (EC), black carbon (BC), pyrolytic carbon (PyrC), optical carbon (OptC), water-soluble organic carbon (WSOC), levoglucosan (LG), mannosan (MNS), and galactosan (GA) were determined in PM₁₀ and PM_2.5 fractions (particles smaller than 10 µm and 2.5 µm, respectively). The annual mean concentrations of PM₁₀ and PM_2.5 were 14 µg/m³ and 8 µg/m³, respectively. During the fire episode, the PM_2.5 mass contribution to the total PM₁₀ mass exceeded 65%. Total carbon (TC) and OC increased by a factor of 7, EC and BC by 12, PyrC by 8, and WSOC by 12. The concentration of LG reached 1.219 μg/m³ in the PM₁₀ fractions and 0.954 μg/m³ in the PM_2.5 fractions, representing a 200-fold increase during the fire episode. Meteorological data were integrated to assess atmospheric conditions during the fire episode, and the specific ratios between fire-related compounds were analyzed.

Levoglucosan (LG), a tracer of biomass-burning air pollution, was measured in PM₁₀ particulate matter during a year-long study at an urban background site in Zagreb, Croatia. It is known that the atmospheric lifetime of LG is not constant and undergoes degradation through reactions with hydroxyl radicals, ozone, photooxidation, etc. In this study, daily variations in LG were examined and evaluated in relation to NO₂, O₃, and meteorological conditions, including temperature, relative humidity, solar irradiance, UV index, and wind characteristics. The annual mean PM₁₀ concentration was 22 µg m⁻³, while LG average was 0.312 µg m⁻³, both exhibiting pronounced seasonal variability. Elevated LG levels occurred during winter and autumn, consistent with residential wood combustion and stable atmospheric conditions, whereas markedly lower concentrations were observed in spring and summer. Moderate correlations of LG with PM₁₀ and NO₂ indicate contributions from combustion sources, while weak wind speeds and limited dispersion favored pollutant accumulation. In contrast, significant negative relationships were found between LG and ozone, temperature, and UV index. The results revealed non-linear behavior and an exponential decrease in LG with increasing oxidant levels, suggesting pseudo–first-order degradation driven by enhanced photochemical activity and hydroxyl radical formation. These findings highlight the importance of considering both emission patterns and atmospheric processing when using levoglucosan as a tracer of biomass burning in urban environments.