Abstract. In recent years, satellite remote sensing has been increasingly used in the long-term observation of ozone (O3) precursors and its formation regime. In this work, formaldehyde (HCHO) data from Ozone Monitoring Instrument (OMI) were used to analyze the temporal and spatial distribution of HCHO vertical column densities (VCDs) in Shanghai from 2010 to 2019. HCHO VCDs exhibited the highest value in summer and the lowest in winter, the high VCD being concentrated in western Shanghai. Temperature largely influences HCHO by affecting the biogenic emissions and photochemical reactions, and industry was the major anthropogenic source. The satellite-observed formaldehyde-to-nitrogen dioxide ratio (FNRSAT) reflects that the O3 formation regime had significant seasonal characteristics and gradually manifested as a transitional ozone formation regime dominating in Shanghai. The uneven distribution in space was mainly reflected in the higher FNRSAT and surface O3 concentration in suburban areas. To compensate for the shortcoming of FNRSAT that it can only characterize O3 formation around satellite overpass time, correction of FNRSAT was implemented with hourly surface FNR and O3 data. After correction, the O3 formation regime showed the trend moving towards being VOC-limited in both time and space, and the regime indicated by FNRSAT can better reflect O3 formation for a day. This study can help us better understand HCHO characteristics and O3 formation regimes in Shanghai and also provide a method to improve FNRSAT for characterizing O3 formation in a day, which will be significant for developing O3 prevention and control strategies.

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.

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. Nitrogen dioxide (NO2) is a major air pollutant. Tropospheric NO2 vertical column densities (VCDs) retrieved from sun-synchronous satellite instruments have provided abundant NO2 data for environmental studies, but such data are limited by insufficient temporal sampling (e.g., once a day). The Geostationary Environment Monitoring Spectrometer (GEMS) launched in February 2020 monitors NO2 at an unprecedented high temporal resolution. Here we present a research product for tropospheric NO2 VCDs, referred to as POMINO-GEMS. We develop a hybrid retrieval method combining GEMS and TROPOMI observations as well as GEOS-Chem simulations to generate hourly tropospheric NO2 slant column densities (SCDs). We then derive tropospheric NO2 air mass factors (AMFs) with explicit corrections for the anisotropy of surface reflectance and aerosol optical effects, through pixel-by-pixel radiative transfer calculations. Prerequisite cloud parameters are retrieved with the O2-O2 algorithm by using ancillary parameters consistent with those used in NO2 AMF calculations. Initial retrieval of POMINO-GEMS tropospheric NO2 VCDs for June–August 2021 reveals strong hotspot signals over megacities and distinctive diurnal variations over polluted and clean areas. POMINO-GEMS NO2 VCDs agree well with our POMINO-TROPOMI v1.2.2 product (R = 0.97, and NMB = 3.6 %) over Asia. Comparison with ground-based MAX-DOAS VCD data at nine sites shows a small bias of POMINO-GEMS (NMB = –15.7 %); however, the correlation for diurnal variation varies from -0.66 to 0.90, suggesting location-dependent performance. Surface NO2 concentrations estimated from POMINO-GEMS VCDs are consistent with measurements from the Ministry of Ecology and Environment of China at 855 sites (NMB = –24.1 %, and R = 0.95 for diurnal correlation averaged over all sites). POMINO-GEMS data will be made freely available for users to study the spatiotemporal variations, sources and impacts of NO2.

No abstract