ORCID Profile
0000-0002-0073-7809
Current Organisation
The Chinese University of Hong Kong
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Publisher: Springer Science and Business Media LLC
Date: 14-10-2019
Publisher: Copernicus GmbH
Date: 26-01-2023
DOI: 10.5194/EGUSPHERE-2022-1485
Abstract: Abstract. Air quality network data in China and South Korea show very high year-round mass concentrations of coarse particulate matter (PM), as inferred by difference between PM10 and PM2.5. Coarse PM concentrations in 2015 averaged 52 μg m-3 in the North China Plain (NCP) and 23 μg m-3 in the Seoul Metropolitan Area (SMA), contributing nearly half of PM10. Strong daily correlations between coarse PM and carbon monoxide imply a dominant source from anthropogenic fugitive dust. Coarse PM concentrations in the NCP and the SMA decreased by 21 % from 2015 to 2019 and further dropped abruptly in 2020 due to COVID-19 reductions in construction and vehicle traffic. Anthropogenic coarse PM is generally not included in air quality models but scavenges nitric acid to suppress the formation of fine particulate nitrate, a major contributor to PM2.5 pollution. GEOS-Chem model simulation of surface and aircraft observations from the KORUS-AQ c aign over the SMA in May–June 2016 shows that consideration of anthropogenic coarse PM largely resolves the previous model overestimate of fine particulate nitrate. The effect is smaller in the NCP which has a larger excess of ammonia. Model sensitivity simulations show that decreasing anthropogenic coarse PM over 2015–2019 directly increases PM2.5 nitrate in summer, offsetting half the effect of other emission controls, while in winter it increases the sensitivity of PM2.5 nitrate to ammonia and sulfur dioxide emissions. Decreasing coarse PM helps to explain the flat wintertime PM2.5 nitrate trends observed in the NCP and the SMA despite decreases in nitrogen oxides and ammonia emissions. The continuing decrease of coarse PM from abating fugitive dust pollution will require more stringent nitrogen oxides and ammonia emission controls to successfully decrease PM2.5 nitrate.
Publisher: Copernicus GmbH
Date: 12-04-2023
Abstract: Abstract. Air quality network data in China and South Korea show very high year-round mass concentrations of coarse particulate matter (PM), as inferred by the difference between PM10 and PM2.5. Coarse PM concentrations in 2015 averaged 52 µg m−3 in the North China Plain (NCP) and 23 µg m−3 in the Seoul Metropolitan Area (SMA), contributing nearly half of PM10. Strong daily correlations between coarse PM and carbon monoxide imply a dominant source from anthropogenic fugitive dust. Coarse PM concentrations in the NCP and the SMA decreased by 21 % from 2015 to 2019 and further dropped abruptly in 2020 due to COVID-19 reductions in construction and vehicle traffic. Anthropogenic coarse PM is generally not included in air quality models but scavenges nitric acid to suppress the formation of fine particulate nitrate, a major contributor to PM2.5 pollution. GEOS-Chem model simulation of surface and aircraft observations from the Korea–United States Air Quality (KORUS-AQ) c aign over the SMA in May–June 2016 shows that consideration of anthropogenic coarse PM largely resolves the previous model overestimate of fine particulate nitrate. The effect is smaller in the NCP which has a larger excess of ammonia. Model sensitivity simulations for 2015–2019 show that decreasing anthropogenic coarse PM directly increases PM2.5 nitrate in summer, offsetting 80 % the effect of nitrogen oxide and ammonia emission controls, while in winter the presence of coarse PM increases the sensitivity of PM2.5 nitrate to ammonia and sulfur dioxide emissions. Decreasing coarse PM helps to explain the lack of decrease in wintertime PM2.5 nitrate observed in the NCP and the SMA over the 2015–2021 period despite decreases in nitrogen oxide and ammonia emissions. Continuing decrease of fugitive dust pollution means that more stringent nitrogen oxide and ammonia emission controls will be required to successfully decrease PM2.5 nitrate.
Publisher: Copernicus GmbH
Date: 18-11-2021
DOI: 10.5194/ACP-21-16775-2021
Abstract: Abstract. Geostationary satellite measurements of aerosol optical depth (AOD) over East Asia from the Geostationary Ocean Color Imager (GOCI) and Advanced Himawari Imager (AHI) instruments can augment surface monitoring of fine particulate matter (PM2.5) air quality, but this requires better understanding of the AOD–PM2.5 relationship. Here we use the GEOS-Chem chemical transport model to analyze the critical variables determining the AOD–PM2.5 relationship over East Asia by simulation of observations from satellite, aircraft, and ground-based datasets. This includes the detailed vertical aerosol profiling over South Korea from the KORUS-AQ aircraft c aign (May–June 2016) with concurrent ground-based PM2.5 composition, PM10, and AERONET AOD measurements. The KORUS-AQ data show that 550 nm AOD is mainly contributed by sulfate–nitrate–ammonium (SNA) and organic aerosols in the planetary boundary layer (PBL), despite large dust concentrations in the free troposphere, reflecting the optically effective size and high hygroscopicity of the PBL aerosols. We updated SNA and organic aerosol size distributions in GEOS-Chem to represent aerosol optical properties over East Asia by using in situ measurements of particle size distributions from KORUS-AQ. We find that SNA and organic aerosols over East Asia have larger size (number median radius of 0.11 µm with geometric standard deviation of 1.4) and 20 % larger mass extinction efficiency as compared to aerosols over North America (default setting in GEOS-Chem). Although GEOS-Chem is successful in reproducing the KORUS-AQ vertical profiles of aerosol mass, its ability to link AOD to PM2.5 is limited by under-accounting of coarse PM and by a large overestimate of nighttime PM2.5 nitrate. The GOCI–AHI AOD data over East Asia in different seasons show agreement with AERONET AODs and a spatial distribution consistent with surface PM2.5 network data. The AOD observations over North China show a summer maximum and winter minimum, opposite in phase to surface PM2.5. This is due to low PBL depths compounded by high residential coal emissions in winter and high relative humidity (RH) in summer. Seasonality of AOD and PM2.5 over South Korea is much weaker, reflecting weaker variation in PBL depth and lack of residential coal emissions.
Publisher: Springer Science and Business Media LLC
Date: 26-04-2021
Publisher: Copernicus GmbH
Date: 29-08-2019
DOI: 10.5194/ACP-19-11031-2019
Abstract: Abstract. Fine particulate matter (PM2.5) is a severe air pollution problem in China. Observations of PM2.5 have been available since 2013 from a large network operated by the China National Environmental Monitoring Center (CNEMC). The data show a general 30 %–50 % decrease in annual mean PM2.5 across China over the 2013–2018 period, averaging at −5.2 µg m−3 a−1. Trends in the five megacity cluster regions targeted by the government for air quality control are -9.3±1.8 µg m−3 a−1 (±95 % confidence interval) for Beijing–Tianjin–Hebei, -6.1±1.1 µg m−3 a−1 for the Yangtze River Delta, -2.7±0.8 µg m−3 a−1 for the Pearl River Delta, -6.7±1.3 µg m−3 a−1 for the Sichuan Basin, and -6.5±2.5 µg m−3 a−1 for the Fenwei Plain (Xi'an). Concurrent 2013–2018 observations of sulfur dioxide (SO2) and carbon monoxide (CO) show that the declines in PM2.5 are qualitatively consistent with drastic controls of emissions from coal combustion. However, there is also a large meteorologically driven interannual variability in PM2.5 that complicates trend attribution. We used a stepwise multiple linear regression (MLR) model to quantify this meteorological contribution to the PM2.5 trends across China. The MLR model correlates the 10 d PM2.5 anomalies to wind speed, precipitation, relative humidity, temperature, and 850 hPa meridional wind velocity (V850). The meteorology-corrected PM2.5 trends after removal of the MLR meteorological contribution can be viewed as being driven by trends in anthropogenic emissions. The mean PM2.5 decrease across China is −4.6 µg m−3 a−1 in the meteorology-corrected data, 12 % weaker than in the original data, meaning that 12 % of the PM2.5 decrease in the original data is attributable to meteorology. The trends in the meteorology-corrected data for the five megacity clusters are -8.0±1.1 µg m−3 a−1 for Beijing–Tianjin–Hebei (14 % weaker than in the original data), -6.3±0.9 µg m−3 a−1 for the Yangtze River Delta (3 % stronger), -2.2±0.5 µg m−3 a−1 for the Pearl River Delta (19 % weaker), -4.9±0.9 µg m−3 a−1 for the Sichuan Basin (27 % weaker), and -5.0±1.9 µg m−3 a−1 for the Fenwei Plain (Xi'an 23 % weaker) 2015–2017 observations of flattening PM2.5 in the Pearl River Delta and increases in the Fenwei Plain can be attributed to meteorology rather than to relaxation of emission controls.
Publisher: Copernicus GmbH
Date: 14-01-2021
Abstract: Abstract. Hydroxymethanesulfonate (HMS) has recently been identified as an abundant organosulfur compound in aerosols during winter haze episodes in northern China. It has also been detected in other regions although the concentrations are low. Because of the sparse field measurements, the global significance of HMS and its spatial and seasonal patterns remain unclear. Here, we modify and add to the implementation of HMS chemistry in the GEOS-Chem chemical transport model and conduct multiple global simulations. The model accounts for cloud entrainment and gas–aqueous mass transfer within the rate expressions for heterogeneous sulfur chemistry. Our simulations can generally reproduce quantitative HMS observations from Beijing and show that East Asia has the highest HMS concentration, followed by Europe and North America. The simulated HMS shows a seasonal pattern with higher values in the colder period. Photochemical oxidizing capacity affects the competition of formaldehyde with oxidants (such as ozone and hydrogen peroxide) for sulfur dioxide and is a key factor influencing the seasonality of HMS. The highest average HMS concentration (1–3 µg m−3) and HMS ∕ sulfate molar ratio (0.1–0.2) are found in northern China in winter. The simulations suggest that aqueous clouds act as the major medium for HMS chemistry while aerosol liquid water may play a role if its rate constant for HMS formation is greatly enhanced compared to cloud water.
Publisher: Copernicus GmbH
Date: 07-02-2020
Abstract: Abstract. Satellite observations of tropospheric NO2 columns are extensively used to infer trends in anthropogenic emissions of nitrogen oxides (NOx≡NO+NO2), but this may be complicated by trends in NOx lifetime. Here we use 2004–2018 observations from the Ozone Monitoring Instrument (OMI) satellite-based instrument (QA4ECV and POMINO v2 retrievals) to examine the seasonality and trends of tropospheric NO2 columns over central–eastern China, and we interpret the results with the GEOS-Chem chemical transport model. The observations show a factor of 3 increase in NO2 columns from summer to winter, which we explain in GEOS-Chem as reflecting a longer NOx lifetime in winter than in summer (21 h versus 5.9 h in 2017). The 2005–2018 summer trends of OMI NO2 closely follow the trends in the Multi-resolution Emission Inventory for China (MEIC), with a rise over the 2005–2011 period and a 25 % decrease since. We find in GEOS-Chem no significant trend of the NOx lifetime in summer, supporting the emission trend reported by the MEIC. The winter trend of OMI NO2 is steeper than in summer over the entire period, which we attribute to a decrease in NOx lifetime at lower NOx emissions. Half of the NOx sink in winter is from N2O5 hydrolysis, which counterintuitively becomes more efficient as NOx emissions decrease due to less titration of ozone at night. The formation of organic nitrates also becomes an increasing sink of NOx as NOx emissions decrease but emissions of volatile organic compounds (VOCs) do not.
Publisher: Copernicus GmbH
Date: 26-01-2023
Publisher: Proceedings of the National Academy of Sciences
Date: 03-2021
Abstract: The North China Plain experiences severe summer ozone pollution, but ozone during winter haze (particulate) pollution events has been very low. Here, we show that the abrupt decrease in nitrogen oxide (NO x ) emissions following the COVID-19 lockdown in January 2020 drove fast ozone production during winter haze events to levels approaching the air quality standard. This fast ozone production was driven by formaldehyde originating from high emissions of volatile organic compounds (VOCs). The COVID-19 experience highlights a general 2013 to 2019 trend of rapidly increasing ozone pollution in winter–spring in China as NO x emissions have decreased. VOC emission controls would mitigate the spreading of ozone pollution into winter–spring with benefits for public health, crop production, and particulate pollution.
Location: China
Location: No location found
Location: United States of America
No related grants have been discovered for Shixian Zhai.