ABSTRACT
Stable atmospheric boundary layer is conducive to the accumulation of atmospheric pollution and the occurrence of fog, and fog has a removal effect on air pollution. In this study, we use the observation and WRF-Chem (Weather Research and Forecasting Model with Chemistry) simulation to analyze the factors affecting the removal efficiency in a continuous fog and haze episode from November 26 to 28, 2018 in Jiangsu Province, such as fog thickness and duration. The results show that the WRF-Chem simulation well reproduces the boundary layer characteristics in the stages of fog formation, development and dissipation. The atmospheric boundary layer provides favorable conditions for the maintenance of fog and air pollution. The inversion layer, with the maximum intensity of 3 °C per 100 m, creates favorable thermal conditions, and the water vapor advection is also conducive to the fog maintenance. The ground observation verifies the wet scavenging of PM2.5 during dense fog events. The scavenging effect is related to the fog duration, and the correlation is positive when the fog is just formed and negative when the fog is dissipating. The PM2.5 concentration decreases from 159 µg m-3 to 38 µg m-3 after the fog lasts for 11 h. The fog has a remarkable scavenging effect on PM2.5 in the vertical direction, due to the deposition effect of fog droplets on the pollutant particles. The PM2.5 concentration on the ground is lower than the vertical average in the fog area, and the scavenging effects during the dense fog periods on November 27 and 28 are 47.7 µg m-3 and 36.1 µg m-3, respectively. The fog duration is mostly concentrated in 3-17 h. When the duration of fog is 4-8 h, the scavenging effect on PM2.5 reaches the strongest, with an average PM2.5 concentration decrease of >70 µg m-3.
ABSTRACT
In this study, aerosol optical depth (AOD) and extinction Ångström exponent (EAE) are derived from ground-based sunphotometer observations between 2007 and 2014 at urban sites of Nanjing over the Yangtze River Delta. In addition, the present study aims to investigate aerosol light-absorbing properties such as single-scattering albedo (SSA), absorption Ångström exponent (AAE), and the aerosol-absorbing optical depth (AAOD). The retrieval of aerosol properties is compared with AERONET inversion products. The results demonstrate that the retrieved AOD has a good agreement with the AERONET Level 1.5 data, with the root mean square error being 0.068, 0.065, and 0.026 for total, fine mode, and coarse mode at 440 nm, respectively. The SSA values indicate similar accuracies in the results, which are about 0.003, -0.009, -0.008, and 0.010 different from AERONET at 440, 670, 870, and 1020 nm, respectively. The occurrence frequency of background level AOD (AOD<0.10) at 440 nm in this region is limited (1%). Monthly mean AOD, SSA, the effective radius (Reff), and the volume concentration at 440 nm were 0.6-1.3, 0.85-0.92, 0.24-0.40 µm, and 0.18-0.28 µm3 µm-2, respectively. The mean value of AAOD at 440 nm (AAOD440) was the highest in both summer (0.095±0.041) and autumn (0.094±0.042), but was the lowest in winter (0.079±0.036). It was also noted that SSA was found to be higher during summer (0.89±0.05). The spectral variation of SSA was observed to be strongly wavelength-dependent during all seasons. The seasonal mean AAE440-870 is the highest in winter (0.86±0.41) and lowest in spring (0.49±0.29). In winter, the cumulative frequency for AAE between 1.0 and 1.2 was about 87%. The peak in the AAE distribution was close to 1.0, indicating that the aerosol column was dominated by urban-industrial aerosols and absorption species other than black carbon. Analysis of the relationship between EAE and SSA showed that the aerosol populations could be classified as "mixed" aerosol, including a mixture of both anthropogenic particles and secondary organic aerosol with highly variable sphericity fraction.
