Intense economic and industrial development in China has been accompanied by severe local air pollution, as well as in other downwind countries in East Asia. This study analyzes satellite observational data of sulfur dioxide (SO₂), nitrogen dioxide (NO₂), and aerosol optical depth (AOD) to explore the spatial distribution, long-term temporal variation, and correlation to meteorological conditions over this region over the period 2005–2015. SO₂ and NO₂ data are retrieved from the ozone monitoring instrument (OMI) onboard the National Aeronautics and Space Administration (NASA) Aura satellite, while AOD data are from the moderate-resolution imaging spectroradiometer (MODIS) onboard the NASA Aqua satellite. Spatial distributions of SO₂, NO₂, and AOD show the highest levels in the North China Plain (NCP), with hotspots also in Southeastern China (SC) and the Sichuan Basin (SB). Biomass burning also contributes to a high level of AOD in Southeast Asia in spring and in Equatorial Asia in fall. Considering the correlation of pollutant levels to meteorological conditions, monitoring data show that higher temperature and higher relative humidity (RH) favor the conversion of SO₂ and NO₂ to sulfate and nitrate aerosol, respectively. The impact of stronger lower tropospheric stability facilitates the accumulation of SO₂ and NO₂ in NCP and SC. Transport of SO₂ and NO₂ from intense source regions to relatively clean regions is highly influential over East Asia; such transport from the NCP leads to a considerable increase of pollutants in SC, SB, Taiwan Island (TW), and Taiwan Strait (TWS), particularly in winter. Aerosols generated by biomass burning in Southeast Asia and anthropogenic aerosol in SC are transported to TW and TWS and lead to the increase of AOD, with the highest levels of AOD in SC, TW, and TWS occurring in spring. Precipitation results in the removal of pollutants, especially in highly polluted regions, the effect of which is most significant in winter and spring.

To study the effect of giant cloud condensation nuclei (GCCN) on precipitation processes in stratocumulus clouds, 1–10 μm diameter salt particles (salt powder) were released from an aircraft while flying near the cloud top on 3 August 2011 off the central coast of California. The seeded area was subsequently sampled from the aircraft that was equipped with aerosol, cloud, and precipitation probes and an upward-facing cloud radar. During post-seeding sampling, made 30–60 min after seeding, the mean cloud droplet size increased, the droplet number concentration decreased, and large drop (e.g., diameter larger than 10 μm) concentration increased. Average drizzle rates increased from about 0.05 to 0.20 mm h⁻¹, and the liquid water path decreased from about 52 to 43 g m⁻². Strong radar returns associated with drizzle were observed on the post-seeding cloud-base level-leg flights and were accompanied by a substantial depletion of the cloud liquid water content. The changes were large enough to suggest that the salt particles with concentrations estimated to be 10⁻² to 10^-4 cm⁻³ resulted in a four-fold increase in the cloud-base rainfall rate and depletion of the cloud water due to rainout. In contrast, a case is shown where the cloud was already precipitating (on 10 August) and the effect of adding GCCN to the cloud was insignificant.