An Application of Artificial Neural Network to Evaluate the Influence of Weather Conditions on the Variation of PM2.5-Bound Carbonaceous Compositions and Water-Soluble Ionic Species

Previous studies have determined biomass burning as a major source of air pollutants in the ambient air in Thailand. To analyse the impacts of meteorological parameters on the variation of carbonaceous aerosols and water-soluble ionic species (WSIS), numerous statistical models, including a source apportionment analysis with the assistance of principal component analysis (PCA), hierarchical cluster analysis (HCA), and artificial neural networks (ANNs), were employed in this study. A total of 191 sets of PM2.5 samples were collected from the three monitoring stations in Chiang-Mai, Bangkok, and Phuket from July 2020 to June 2021. Hotspot numbers and other meteorological parameters were obtained using NOAA-20 weather satellites coupled with the Global Land Data Assimilation System. Although PCA revealed that crop residue burning and wildfires are the two main sources of PM2.5, ANNs highlighted the importance of wet deposition as the main depletion mechanism of particulate WSIS and carbonaceous aerosols. Additionally, Mg2+ and Ca2+ were deeply connected with albedo, plausibly owing to their strong hygroscopicity as the CCNs responsible for cloud formation.

Measurement report: The importance of biomass burning in light extinction and direct radiative effect of urban aerosol during the COVID-19 lockdown in Xi'an, China

Due to the complexity of emission sources, a better understanding of aerosol optical properties is required to mitigate climate change in China. Here, an intensive real-time measurement campaign was conducted in an urban area of China before and during the COVID-19 lockdown in order to explore the impacts of anthropogenic activities on aerosol light extinction and the direct radiative effect (DRE). The mean light extinction coefficient (bext) decreased from 774.7 ± 298.1 Mm-1 during the normal period to 544.3 ± 179.4 Mm-1 during the lockdown period. A generalised additive model analysis indicated that the large decline in bext (29.7 %) was due to sharp reductions in anthropogenic emissions. Chemical calculation of bext based on a ridge regression analysis showed that organic aerosol (OA) was the largest contributor to bext in both periods (45.1 %–61.4 %), and the contributions of two oxygenated OAs to bext increased by 3.0 %–14.6 % during the lockdown. A hybrid environmental receptor model combined with chemical and optical variables identified six sources of bext. It was found thatbext from traffic-related emissions, coal combustion, fugitive dust, the nitrate and secondary OA (SOA) source, and the sulfate and SOA source decreased by 21.4 %–97.9 % in the lockdown, whereas bext from biomass burning increased by 27.1 %, mainly driven by the undiminished need for residential cooking and heating. An atmospheric radiative transfer model was further used to illustrate that biomass burning, rather than traffic-related emissions, became the largest positive effect (10.0 ± 10.9 W m-2) on aerosol DRE in the atmosphere during the lockdown. Our study provides insights into aerosol bext and DRE from anthropogenic sources, and the results imply the importance of controlling biomass burning for tackling climate change in China in the future.

Impact of reduced anthropogenic emissions on chemical characteristics of urban aerosol by individual particle analysis.

A single particle aerosol mass spectrometer was deployed in a heavily polluted area of China during a coronavirus lockdown to explore the impact of reduced anthropogenic emissions on the chemical composition, size distributions, mixing state, and secondary formation of urban aerosols. Ten particle groups were identified using an adaptive resonance network algorithm. Increased atmospheric oxidation during the lockdown period (LP) resulted in a 42.2%-54% increase in the major NaK-SN particle fraction relative to the normal period (NP). In contrast, EC-aged particles decreased from 31.5% (NP) to 23.7% (LP), possibly due to lower emissions from motor vehicles and coal combustion. The peak particle size diameter increased from 440 nm during the NP to 500 nm during LP due to secondary particle formation. High proportions of mixed 62NO3- indicate extensive particle aging. Correlations between secondary organic (43C2H3O+, oxalate) and secondary inorganic species (62NO3-, 97HSO4- and 18NH4+) versus oxidants (Ox = O3 + NO2) and relative humidity (RH) indicate that increased atmospheric oxidation promoted the generation of secondary species, while the effects of RH were more complex. Differences between the NP and LP show that reductions in primary emissions had a remarkable impact on the aerosol particles. This study provides new insights into the effects of pollution emissions on atmospheric reactions and the specific aerosol types in urban regions.

Impact of COVID-19 lockdown on the optical properties and radiative effects of urban brown carbon aerosol

Intensive measurements were conducted in Xi’an, China before and during a COVID-19 lockdown period to investigate how changes in anthropogenic emissions affected the optical properties and radiative effects of brown carbon (BrC) aerosol. The contribution of BrC to total aerosol light absorption during the lockdown (13%–49%) was higher compared with the normal period (4%–29%). Mass absorption cross-sections (MAC) of specific organic aerosol (OA) factors were calculated from a ridge regression model. Of the primary OA (POA), coal combustion OA (CCOA) had the largest MACs at all tested wavelengths during both periods due to high molecular-weight BrC chromophores;that was followed by biomass burning OA (BBOA) and hydrocarbon-like OA (HOA). For secondary OA (SOA), the MACs of the less-oxidized oxygenated OA (OOA) species (LO-OOA) at λ = 370–590 nm were higher than those of more-oxidized OOA (MO-OOA) during both periods, presumably due to chromophore bleaching. The largest contributor to BrC absorption at the short wavelengths was CCOA during both periods, but BrC absorption by LO-OOA and MO-OOA became dominant at longer wavelengths during the lockdown. The estimated radiation forcing efficiency of BrC over 370–600 nm increased from 37.5 W· g-1 during the normal period to 50.2 W·g-1 during the lockdown, and that enhancement was mainly caused by higher MACs for both LO-OOA and MO-OOA. This study provides insights into the optical properties and radiative effects of source-specific BrC aerosol when pollution emissions are reduced.