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The lack of vertical observation of reactive nitrogen oxides in agricultural areas has posed a significant challenge in fully understanding their sources and impacts on atmospheric oxidation. Ground-based multi-axis differential optical absorption spectroscopy (MAX-DOAS) observations were conducted in the agricultural regions of the North China Plain (NCP) during the summer of 2019 to measure the vertical distributions of aerosols, nitrogen dioxide (NO2), and nitrous acid (HONO). This study aimed at revealing the spatiotemporal distribution, sources, and environmental effects of reactive nitrogen oxides in the NCP agricultural areas. Our findings indicated that the vertical profiles of aerosols and NO2 exhibited a near-Gaussian distribution, with distinct peak times occurring between 8:00–10:00 and 16:00–18:00. HONO reached its maximum concentration near the surface around 8:00 in the morning and decreased exponentially with altitude. After sunrise, the concentration of HONO rapidly decreased due to photolysis. Additionally, the potential source contribution function (PSCF) was used to evaluate the potential sources of air pollutants. The results indicated that the main potential pollution sources of aerosols were located in the southern part of the Hebei, Shanxi, Shandong, and Jiangsu provinces, while the potential pollution sources of NO2 were concentrated in the Beijing–Tianjin–Hebei region. At altitudes exceeding 500 m, the heterogeneous reactions of NO2 on aerosol surfaces were identified as one of the important contributors to the formation of HONO. Furthermore, we discussed the production rate of hydroxyl radicals (OH) from HONO photolysis. It was found that the production rate of OH from HONO photolysis decreased with altitude, with peaks occurring in the morning and late afternoon. This pattern was consistent with the variations in HONO concentration, indicating that HONO was the main contributor to OH production in the agricultural regions of the NCP. This study provides a new perspective on the sources of active nitrogen in agricultural regions and their contribution to atmospheric oxidation capacity from a vertical perspective. [ABSTRACT FROM AUTHOR]

The long-path differential optical absorption spectroscopy (LP-DOAS) technique was deployed in Shanghai to continuously monitor ozone (O3), formaldehyde (HCHO), nitrogen dioxide (NO2), nitrous acid (HONO), and nitrate radical (NO3) mixing ratios from September 2019 to August 2020. Through a clustering method, four typical clusters of the O3 diurnal pattern were identified: high during both the daytime and nighttime (cluster 1), high during the nighttime but low during the daytime (cluster 2), low during both the daytime and nighttime (cluster 3), and low during the nighttime but high during the daytime (cluster 4). The drivers of O3 variation for the four clusters were investigated for the day- and nighttime. Ambient NO caused the O3 gap after midnight between clusters 1 and 2 and clusters 3 and 4. During the daytime, vigorous O3 generation (clusters 1 and 4) was found to accompany higher temperature, lower humidity, lower wind speed, and higher radiation. Moreover, O3 concentration correlated with HCHO for all clusters except for the low O3 cluster 3, while O3 correlated with HCHO/NOx, but anti-correlated with NOx for all clusters. The lower boundary layer height before midnight hindered O3 diffusion and accordingly determined the final O3 accumulation over the daily cycle for clusters 1 and 4. The interactions between the O3 diel profile and other atmospheric reactive components established that higher HONO before sunrise significantly promoted daytime O3 generation, while higher daytime O3 led to a higher nighttime NO3 level. This paper summarizes the interplays between day- and nighttime oxidants and oxidation products, particularly the cause and effect for daytime O3 generation from the perspective of nighttime atmospheric components. [ABSTRACT FROM AUTHOR]

Recently, the occurrence of fog and haze over China has increased. The retrieval of trace gases from the multi-axis differential optical absorption spectroscopy (MAX-DOAS) is challenging under these conditions. In this study, various reported retrieval settings for formaldehyde (HCHO) and sulfur dioxide (SO2) are compared to evaluate the performance of these settings under different meteorological conditions (clear day, haze, and fog). The dataset from 1st December 2019 to 31st March 2020 over Nanjing, China, is used in this study. The results indicated that for HCHO, the optimal settings were in the 324.5–359 nm wavelength window with a polynomial order of five. At these settings, the fitting and root mean squared (RMS) errors for column density were considerably improved for haze and fog conditions, and the differential slant column densities (DSCDs) showed more accurate values compared to the DSCDs between 336.5 and 359 nm. For SO2, the optimal settings for retrieval were found to be at 307–328 nm with a polynomial order of five. Here, root mean square (RMS) and fitting errors were significantly lower under all conditions. The observed HCHO and SO2 vertical column densities were significantly lower on fog days compared to clear days, reflecting a decreased chemical production of HCHO and aqueous phase oxidation of SO2 in fog droplets. [ABSTRACT FROM AUTHOR]

Reduced mobility and less anthropogenic activity under special case circumstances over various parts of the world have pronounced effects on air quality. The objective of this study is to investigate the impact of reduced anthropogenic activity on air quality in the mega city of Shanghai, China. Observations from the highly sophisticated multi-axis differential optical absorption spectroscope (MAX-DOAS) instrument were used for nitrogen dioxide (NO2) and formaldehyde (HCHO) column densities. In situ measurements for NO2, ozone (O3), particulate matter (PM2.5) and the air quality index (AQI) were also used. The concentration of trace gases in the atmosphere reduces significantly during annual Spring Festival holidays, whereby mobility is reduced and anthropogenic activities come to a halt. The COVID-19 lockdown during 2020 resulted in a considerable drop in vertical column densities (VCDs) of HCHO and NO2 during lockdown Level-1, which refers to strict lockdown, i.e., strict measures taken to reduce mobility (43% for NO2; 24% for HCHO), and lockdown Level-2, which refers to relaxed lockdown, i.e., when the mobility restrictions were relaxed somehow (20% for NO2; 22% for HCHO), compared with pre-lockdown days, as measured by the MAX-DOAS instrument. However, for 2019, a reduction in VCDs was found only during Level-1 (24% for NO2; 6.62% for HCHO), when the Spring Festival happened. The weekly cycle for NO2 and HCHO depicts no significant effect of weekends on the lockdown. After the start of the Spring Festival, the VCDs of NO2 and HCHO showed a decline for 2019 as well as 2020. Backward trajectories calculated using the Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) model indicated more air masses coming from the sea after the Spring Festival for 2019 and 2020, implying that a low pollutant load was carried by them. No impact of anthropogenic activity was found on O3 concentration. The results indicate that the ratio of HCHO to NO2 (RFN) fell in the volatile organic compound (VOC)-limited regime. [ABSTRACT FROM AUTHOR]