scholarly journals Regional atmospheric pollutant transport mechanisms over the North China Plain driven by topography and planetary boundary layer processes

2020 ◽  
Vol 221 ◽  
pp. 117098 ◽  
Author(s):  
Jiannong Quan ◽  
Youjun Dou ◽  
Xiujuan Zhao ◽  
Quan Liu ◽  
Zhaobin Sun ◽  
...  
2020 ◽  
Vol 240 ◽  
pp. 104930 ◽  
Author(s):  
Shuang Wu ◽  
Guiqian Tang ◽  
Yinghong Wang ◽  
Yang Yang ◽  
Dan Yao ◽  
...  

2018 ◽  
Author(s):  
Tianning Su ◽  
Zhanqing Li ◽  
Ralph Kahn

Abstract. The frequent occurrence of severe air pollution episodes in China has raised great concerns with the public and scientific communities. Planetary boundary layer height (PBLH) is a key factor in the vertical mixing and dilution of near-surface pollutants. However, the relationship between PBLH and surface pollutants, especially particulate matter (PM) concentration, across the whole of China, is not yet well understood. We investigate this issue at ~ 1500 surface stations using PBLH derived from space-borne and ground-based lidar, and discuss the influence of topography and meteorological variables on the PBLH-PM relationship. A generally negative correlation is observed between PM and the PBLH, albeit varying greatly in magnitude with location and season. Correlations are much weaker over the highlands than plains regions, which may be associated with lower pollution levels and mountain breezes. The influence of horizontal transport on surface PM is considered as well, manifested as a negative correlation between surface PM and wind speed over the whole nation. Strong wind with clean upwind sources plays a dominant role in removing pollutants, and leads to weak PBLH-PM correlation. A ventilation rate is introduced to jointly consider horizontal and vertical dispersion, which has the largest impact on surface pollutant accumulation over the North China Plain. Aerosol absorption feedbacks also appear to affect the PBLH-PM relationship, as revealed via comparing air pollution in Beijing and Hong Kong. Absorbing aerosols in high concentrations likely contribute to the significant PBLH-PM correlation over the North China Plain (e.g., during winter). As major precursor emissions for secondary aerosols, sulfur dioxide, nitrogen dioxide, and carbon monoxide have similar negative responses to increased PBLH, whereas ozone is positively correlated with PBLH over most regions, which may be caused by heterogeneous reactions and photolysis rates.


2020 ◽  
Vol 20 (20) ◽  
pp. 12115-12131
Author(s):  
Ying Jiang ◽  
Likun Xue ◽  
Rongrong Gu ◽  
Mengwei Jia ◽  
Yingnan Zhang ◽  
...  

Abstract. Nitrous acid (HONO) is a significant precursor of atmospheric “detergent” OH radicals and plays a vital role in tropospheric chemistry. The current knowledge about daytime HONO sources is incomplete, and its impact on the tropospheric radical chemistry has not been fully quantified. Existing observational studies of HONO were mostly conducted at the surface, with few efforts focusing on the high-elevation atmosphere. In order to better understand the characteristics and sources of HONO in the upper boundary layer and lower free troposphere, two intensive field observations were carried out at the summit of Mt. Tai (1534 m a.s.l.), the peak of the North China Plain (NCP), in winter 2017 and spring 2018. HONO showed moderate concentration levels (average ± standard deviation: 0.15±0.15 and 0.13±0.15 ppbv), with maximum values of 1.14 and 3.23 ppbv in winter and spring, respectively. Diurnal variation patterns with broad noontime maxima and lower nighttime concentrations were observed during both campaigns, which is distinct from most of the previous studies at the ground level. The Lagrangian particle dispersion model (LPDM, WRF-FLEXPART v3.3) simulations indicated the combined effects of the planetary boundary layer evolution and valley breeze on the daytime HONO peak. A photostationary state (PSS) analysis suggested a strong unknown daytime HONO source with production rates of 0.45±0.25 ppb h−1 in winter and 0.64±0.49 ppb h−1 in spring. Correlation analysis supported the important role of photo-enhanced heterogeneous conversion of NO2 to HONO on the aerosol surface at this high-elevation site. HONO photolysis is the predominant primary source of OH radical and plays a major role in the radical chemistry at Mt. Tai. The model only considering a homogenous HONO source predicted much lower levels of the HOx radicals and atmospheric oxidation capacity than the model constrained with measured HONO data. This study sheds light on the characteristics, sources, chemistry, and impacts of HONO in the upper boundary layer and lower free troposphere in the NCP region.


2019 ◽  
Vol 83 ◽  
pp. 152-160 ◽  
Author(s):  
Wei Zhao ◽  
Guiqian Tang ◽  
Huan Yu ◽  
Yang Yang ◽  
Yinghong Wang ◽  
...  

2014 ◽  
Vol 41 (2) ◽  
pp. 645-651 ◽  
Author(s):  
Anne Boynard ◽  
Cathy Clerbaux ◽  
Lieven Clarisse ◽  
Sarah Safieddine ◽  
Matthieu Pommier ◽  
...  

2015 ◽  
Vol 15 (8) ◽  
pp. 4279-4295 ◽  
Author(s):  
Y. Gao ◽  
M. Zhang ◽  
Z. Liu ◽  
L. Wang ◽  
P. Wang ◽  
...  

Abstract. The feedback between aerosol and meteorological variables in the atmospheric boundary layer over the North China Plain (NCP) is analyzed by conducting numerical experiments with and without the aerosol direct and indirect effects via a coupled meteorology and aerosol/chemistry model (WRF-Chem). The numerical experiments are performed for the period of 2–26 January 2013, during which a severe fog–haze event (10–15 January 2013) occurred, with the simulated maximum hourly surface PM2.5 concentration of ~600 ug m−3, minimum atmospheric visibility of ~0.3 km, and 10–100 hours of simulated hourly surface PM2.5 concentration above 300 ug m−3 over NCP. A comparison of model results with aerosol feedback against observations indicates that the model can reproduce the spatial and temporal characteristics of temperature, relative humidity (RH), wind, surface PM2.5 concentration, atmospheric visibility, and aerosol optical depth reasonably well. Analysis of model results with and without aerosol feedback shows that during the fog–haze event aerosols lead to a significant negative radiative forcing of −20 to −140 W m−2 at the surface and a large positive radiative forcing of 20–120 W m−2 in the atmosphere and induce significant changes in meteorological variables with maximum changes during 09:00–18:00 local time (LT) over urban Beijing and Tianjin and south Hebei: the temperature decreases by 0.8–2.8 °C at the surface and increases by 0.1–0.5 °C at around 925 hPa, while RH increases by about 4–12% at the surface and decreases by 1–6% at around 925 hPa. As a result, the aerosol-induced equivalent potential temperature profile change shows that the atmosphere is much more stable and thus the surface wind speed decreases by up to 0.3 m s−1 (10%) and the atmosphere boundary layer height decreases by 40–200 m (5–30%) during the daytime of this severe fog–haze event. Owing to this more stable atmosphere during 09:00–18:00, 10–15~January, compared to the surface PM2.5 concentration from the model results without aerosol feedback, the average surface PM2.5 concentration increases by 10–50 μg m−3 (2–30%) over Beijing, Tianjin, and south Hebei and the maximum increase of hourly surface PM2.5 concentration is around 50 (70%), 90 (60%), and 80 μg m−3 (40%) over Beijing, Tianjin, and south Hebei, respectively. Although the aerosol concentration is maximum at nighttime, the mechanism of feedback, by which meteorological variables increase the aerosol concentration most, occurs during the daytime (around 10:00 and 16:00 LT). The results suggest that aerosol induces a more stable atmosphere, which is favorable for the accumulation of air pollutants, and thus contributes to the formation of fog–haze events.


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