scholarly journals Aerosol chemistry and particle growth events at an urban downwind site in the North China Plain

2018 ◽  
Author(s):  
Yingjie Zhang ◽  
Wei Du ◽  
Yuying Wang ◽  
Qingqing Wang ◽  
Haofei Wang ◽  
...  
Keyword(s):  
Growth Rates ◽  
North China Plain ◽  
North China ◽  
Particle Growth ◽  
Early Morning ◽  
Scanning Mobility Particle Sizer ◽  
Average Mass ◽  
The North ◽  
The North China Plain ◽  
Haze Pollution

Abstract. The North China Plain (NCP) has experienced frequent severe haze pollution events in recent years. While extensive measurements have been made in megacities, aerosol sources, processes, and particle growth at urban downwind sites remain less understood. Here, an Aerosol Chemical Speciation Monitor and a Scanning Mobility Particle Sizer, along with a suite of collocated instruments, were deployed at the downwind site of Xingtai, a highly polluted city in the NCP, for real-time measurements of submicron aerosol (PM1) species and particle number size distributions during May and June 2016. The average mass concentration of PM1 was 30.5 (±19.4) μg m−3, which is significantly lower than that during wintertime. Organic aerosols (OA) constituted the major fraction of PM1 (38 %) followed by sulfate (25 %) and nitrate (14 %). Positive matrix factorization with the Multilinear Engine version 2 showed that oxygenated OA (OOA) was the dominant species in OA throughout the study, on average accounting for 78 % of OA, while traffic and cooking emissions both accounted for 11 % of OA. Our results highlight that aerosol particles at the urban downwind site were highly aged and mainly from secondary formation. However, the diurnal cycle also illustrated the substantial influence of urban emissions on downwind sites, which are characterized by similar pronounced early morning peaks for most aerosol species. New particle formation and growth events were also frequently observed (58 % of the time) on both clean and polluted days. Particle growth rates varying from 1.2 to 4.9 nm h−1 were positively related to the condensation sink during periods with high OOA contributions and also to sulfate concentrations during relatively clean periods. Our results showed that sulfate and OOA played important roles in particle growth during clean periods, while OOA was more important than sulfate during polluted events. Further analyses showed that particle growth rates have no clear dependence on air mass trajectories.

scholarly journals Aerosol chemistry and particle growth events at an urban downwind site in North China Plain

2018 ◽  
Vol 18 (19) ◽  
pp. 14637-14651 ◽  
Author(s):  
Yingjie Zhang ◽  
Wei Du ◽  
Yuying Wang ◽  
Qingqing Wang ◽  
Haofei Wang ◽  
...  
Keyword(s):  
Growth Rates ◽  
North China Plain ◽  
North China ◽  
Particle Growth ◽  
Early Morning ◽  
Scanning Mobility Particle Sizer ◽  
Average Mass ◽  
The North ◽  
Haze Pollution ◽  
Engine Version

Abstract. The North China Plain (NCP) has experienced frequent severe haze pollution events in recent years. While extensive measurements have been made in megacities, aerosol sources, processes, and particle growth at urban downwind sites remain less understood. Here, an aerosol chemical speciation monitor and a scanning mobility particle sizer, along with a suite of collocated instruments, were deployed at the downwind site of Xingtai, a highly polluted city in the NCP, for real-time measurements of submicron aerosol (PM1) species and particle number size distributions during May and June 2016. The average mass concentration of PM1 was 30.5 (±19.4) µg m−3, which is significantly lower than that during wintertime. Organic aerosols (OAs) constituted the major fraction of PM1 (38 %), followed by sulfate (25 %) and nitrate (14 %). Positive matrix factorization with the multilinear engine version 2 showed that oxygenated OA (OOA) was the dominant species in OA throughout the study, on average accounting for 78 % of OA, while traffic and cooking emissions both accounted for 11 % of OA. Our results highlight that aerosol particles at the urban downwind site were highly aged and mainly from secondary formation. However, the diurnal cycle also illustrated the substantial influence of urban emissions on downwind sites, which are characterized by similar pronounced early morning peaks for most aerosol species. New particle formation and growth events were also frequently observed (58 % of the time) on both clean and polluted days. Particle growth rates varied from 1.2 to 4.9 nm h−1 and our results showed that sulfate and OOA played important roles in particle growth during clean periods, while OOA was more important than sulfate during polluted events. Further analyses showed that particle growth rates have no clear dependence on air mass trajectories.

scholarly journals Aerosol optical depth thresholds as a tool to assess diffuse radiation fertilization of the land carbon uptake in China

2017 ◽  
Vol 17 (2) ◽  
pp. 1329-1342 ◽  
Author(s):  
Xu Yue ◽  
Nadine Unger
Keyword(s):  
Aerosol Optical Depth ◽  
Optical Depth ◽  
North China Plain ◽  
North China ◽  
Carbon Uptake ◽  
The North ◽  
The North China Plain ◽  
Haze Pollution ◽  
Aerosol Pollution ◽  
Sky Conditions

Abstract. China suffers from frequent haze pollution episodes that alter the surface solar radiation and influence regional carbon uptake by the land biosphere. Here, we apply combined vegetation and radiation modeling and multiple observational datasets to assess the radiative effects of aerosol pollution in China on the regional land carbon uptake for the 2009–2011 period. First, we assess the inherent sensitivity of China's land biosphere to aerosol pollution by defining and calculating two thresholds of aerosol optical depth (AOD) at 550 nm, (i) AODt1, resulting in the maximum net primary productivity (NPP), and (ii) AODt2, such that if local AOD < AODt2, the aerosol diffuse fertilization effect (DFE) always promotes local NPP compared with aerosol-free conditions. Then, we apply the thresholds, satellite data, and interactive vegetation modeling to estimate current impacts of aerosol pollution on land ecosystems. In the northeast, observed AOD is 55 % lower than AODt1, indicating a strong aerosol DFE on local NPP. In the southeastern coastal regions, observed AOD is close to AODt1, suggesting that regional NPP is promoted by the current level of aerosol loading, but that further increases in AOD in this region will weaken the fertilization effects. The North China Plain experiences limited enhancement of NPP by aerosols because observed AOD is 77 % higher than AODt1 but 14 % lower than AODt2. Aerosols always inhibit regional NPP in the southwest because of the persistent high cloud coverage that already substantially reduces the total light availability there. Under clear-sky conditions, simulated NPP shows widespread increases of 20–60 % (35.0 ± 0.9 % on average) by aerosols. Under all-sky conditions, aerosol pollution has spatially contrasting opposite sign effects on NPP from −3 % to +6 % (1.6 ± 0.5 % on average), depending on the local AOD relative to the regional thresholds. Stringent aerosol pollution reductions motivated by public health concerns, especially in the North China Plain and the southwest, will help protect land ecosystem functioning in China and mitigate long-term global warming.

scholarly journals Vertical profiles of black carbon measured by a micro-aethalometer in summer in the North China Plain

2016 ◽  
Vol 16 (16) ◽  
pp. 10441-10454 ◽  
Author(s):  
Liang Ran ◽  
Zhaoze Deng ◽  
Xiaobin Xu ◽  
Peng Yan ◽  
Weili Lin ◽  
...  
Keyword(s):  
Black Carbon ◽  
North China Plain ◽  
North China ◽  
Ground Level ◽  
Early Morning ◽  
Vertical Profiles ◽  
Large Variability ◽  
Field Campaign ◽  
The North ◽  
The North China Plain

Abstract. Black carbon (BC) is a dominant absorber in the visible spectrum and a potent factor in climatic effects. Vertical profiles of BC were measured using a micro-aethalometer attached to a tethered balloon during the Vertical Observations of trace Gases and Aerosols (VOGA) field campaign, in summer 2014 at a semirural site in the North China Plain (NCP). The diurnal cycle of BC vertical distributions following the evolution of the mixing layer (ML) was investigated for the first time in the NCP region. Statistical parameters including identified mixing height (Hm) and average BC mass concentrations within the ML (Cm) and in the free troposphere (Cf) were obtained for a selected dataset of 67 vertical profiles. Hm was usually lower than 0.2 km in the early morning and rapidly rose thereafter due to strengthened turbulence. The maximum height of the ML was reached in the late afternoon. The top of a full developed ML exceeded 1 km on sunny days in summer, while it stayed much lower on cloudy  days. The sunset triggered the collapse of the ML, and a stable nocturnal boundary layer (NBL) gradually formed. Accordingly, the highest level Cm was found in the early morning and the lowest was found in the afternoon. In the daytime, BC was almost uniformly distributed within the ML and significantly decreased above the ML. During the field campaign, Cm averaged about 5.16 ± 2.49 µg m−3, with a range of 1.12 to 14.49 µg m−3, comparable with observational results in many polluted urban areas such as Milan in Italy and Shanghai in China. As evening approached, BC gradually built up near the surface and exponentially declined with height. In contrast to the large variability found both in Hm and Cm, Cf stayed relatively unaffected through the day. Cf was less than 10 % of the ground level under clean conditions, while it amounted to half of the ground level in some polluted cases. In situ measurements of BC vertical profiles would hopefully have an important implication for accurately estimating direct radiative forcing by BC and improving the retrieval of aerosol optical properties by remote sensing in this region.

scholarly journals Aerosol–radiation feedback deteriorates the wintertime haze in the North China Plain

2019 ◽  
Vol 19 (13) ◽  
pp. 8703-8719 ◽  
Author(s):  
Jiarui Wu ◽  
Naifang Bei ◽  
Bo Hu ◽  
Suixin Liu ◽  
Meng Zhou ◽  
...  
Keyword(s):  
Solar Radiation ◽  
Air Pollutants ◽  
North China Plain ◽  
North China ◽  
Near Surface ◽  
The North ◽  
The North China Plain ◽  
Incoming Solar Radiation ◽  
Haze Pollution ◽  
Pm2.5 Concentration

Abstract. Atmospheric aerosols scatter or absorb a fraction of the incoming solar radiation to cool or warm the atmosphere, decreasing surface temperature and altering atmospheric stability to further affect the dispersion of air pollutants in the planetary boundary layer (PBL). In the present study, simulations during a persistent and heavy haze pollution episode from 5 December 2015 to 4 January 2016 in the North China Plain (NCP) were performed using the Weather Research and Forecasting model with Chemistry (WRF-Chem) to comprehensively quantify contributions of aerosol shortwave radiative feedback (ARF) to near-surface (around 15 m above the ground surface) PM2.5 mass concentrations. The WRF-Chem model generally performs well in simulating the temporal variations and spatial distributions of air pollutants concentrations compared to observations at ambient monitoring sites in the NCP, and the simulated diurnal variations of aerosol species are also consistent with the measurements in Beijing. Additionally, the model simulates the aerosol radiative properties, the downward shortwave flux, and the PBL height against observations in the NCP well. During the episode, ARF deteriorates the haze pollution, increasing the near-surface PM2.5 concentrations in the NCP by 10.2 µg m−3 or with a contribution of 7.8 % on average. Sensitivity studies have revealed that high loadings of PM2.5 attenuate the incoming solar radiation reaching the surface to cool the low-level atmosphere, suppressing the development of the PBL, decreasing the surface wind speed, further hindering the PM2.5 dispersion, and consequently exacerbating the haze pollution in the NCP. Furthermore, when the near-surface PM2.5 mass concentration increases from around 50 to several hundred µg m−3, ARF contributes to the near-surface PM2.5 by more than 20 % during daytime in the NCP, substantially aggravating the heavy haze formation. However, when the near-surface PM2.5 concentration is less than around 50 µg m−3, ARF generally reduces the near-surface PM2.5 concentration due to the consequent perturbation of atmospheric dynamic fields.

scholarly journals Wintertime aerosol chemistry and haze evolution in an extremely polluted city of the North China Plain: significant contribution from coal and biomass combustion

2017 ◽  
Vol 17 (7) ◽  
pp. 4751-4768 ◽  
Author(s):  
Haiyan Li ◽  
Qi Zhang ◽  
Qiang Zhang ◽  
Chunrong Chen ◽  
Litao Wang ◽  
...  
Keyword(s):  
Air Pollution ◽  
Biomass Burning ◽  
Coal Combustion ◽  
North China Plain ◽  
North China ◽  
Biomass Combustion ◽  
The North ◽  
The North China Plain ◽  
Haze Pollution ◽  
Haze Episode

Abstract. The North China Plain (NCP) frequently experiences heavy haze pollution, particularly during wintertime. In winter 2015–2016, the NCP region suffered several extremely severe haze episodes with air pollution red alerts issued in many cities. We have investigated the sources and aerosol evolution processes of the severe pollution episodes in Handan, a typical industrialized city in the NCP region, using real-time measurements from an intensive field campaign during the winter of 2015–2016. The average (±1σ) concentration of submicron aerosol (PM1) during 3 December 2015–5 February 2016 was 187.6 (±137.5) µg m−3, with the hourly maximum reaching 700.8 µg m−3. Organic was the most abundant component, on average accounting for 45 % of total PM1 mass, followed by sulfate (15 %), nitrate (14 %), ammonium (12 %), chloride (9 %) and black carbon (BC, 5 %). Positive matrix factorization (PMF) with the multilinear engine (ME-2) algorithm identified four major organic aerosol (OA) sources, including traffic emissions represented by a hydrocarbon-like OA (HOA, 7 % of total OA), industrial and residential burning of coal represented by a coal combustion OA (CCOA, 29 % of total OA), open and domestic combustion of wood and crop residuals represented by a biomass burning OA (BBOA, 25 % of total OA), and formation of secondary OA (SOA) in the atmosphere represented by an oxygenated OA (OOA, 39 % of total OA). Emissions of primary OA (POA), which together accounted for 61 % of total OA and 27 % of PM1, are a major cause of air pollution during the winter. Our analysis further uncovered that primary emissions from coal combustion and biomass burning together with secondary formation of sulfate (mainly from SO2 emitted by coal combustion) are important driving factors for haze evolution. However, the bulk composition of PM1 showed comparatively small variations between less polluted periods (daily PM2. 5  ≤  75 µg m−3) and severely polluted periods (daily PM2. 5  >  75 µg m−3), indicating relatively synchronous increases of all aerosol species during haze formation. The case study of a severe haze episode, which lasted 8 days starting with a steady buildup of aerosol pollution followed by a persistently high level of PM1 (326.7–700.8 µg m−3), revealed the significant influence of stagnant meteorological conditions which acerbate air pollution in the Handan region. The haze episode ended with a shift of wind which brought in cleaner air masses from the northwest of Handan and gradually reduced PM1 concentration to  <  50 µg m−3 after 12 h. Aqueous-phase reactions under higher relative humidity (RH) were found to significantly promote the production of secondary inorganic species (especially sulfate) but showed little influence on SOA.

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