scholarly journals Aerosol optical properties in the North China Plain during HaChi campaign: an in-situ optical closure study

2011 ◽  
Vol 11 (3) ◽  
pp. 9567-9605 ◽  
Author(s):  
N. Ma ◽  
C. S. Zhao ◽  
A. Nowak ◽  
T. Müller ◽  
S. Pfeifer ◽  
...  

Abstract. The largest uncertainty in the estimation of radiative forcings on climate stems from atmospheric aerosols. In winter and summer of 2009, two periods of in-situ measurements on aerosol physical and chemical properties were conducted within the HaChi project at Wuqing, a town between Beijing and Tianjin in the North China Plain (NCP). Aerosol optical properties including scattering coefficient (σsp), hemispheric back scattering coefficient (σbsp), absorption coefficient (σap, as well as single scattering albedo (ω) are presented. The characteristics of diurnal and seasonal variations are analyzed together with the meteorological and satellite data. The mean values of σsp, 550 nm of the dry aerosol in winter and summer are 280 ± 253 and 379 ± 251 Mm−1, respectively. The average σap for the two periods are respectively 47 ± 38 and 43 ± 27 Mm−1. The mean values of ω are 0.83 ± 0.05 and 0.87 ± 0.05 for winter and summer, respectively. The relative high levels of σsp and σbsp are representative of the regional polluted aerosol of the North China Plain. Pronounced diurnal cycle of σsp, σap and ω are found, mainly influenced by the evolution of boundary layer and accumulation of local emissions during night-time. Regional transport of pollutants from southwest in the NCP is significant both in winter and summer, while high values of σsp and σap correlate with calm winds in winter, which indicating the significant contribution of local emissions. An optical closure experiment is conducted to better understand uncertainties of the measurements. Good correlations (R>0.98) are found between values measured by nephelometer and values calculated with a modified Mie model. Monte Carlo simulations show an uncertainty of about 30% for the calculations. Considering all possible uncertainties of measurements, calculated σsp and σbsp agree well with measured values, indicating a stable performance of instruments and thus a reliable aerosol optical data.

2011 ◽  
Vol 11 (12) ◽  
pp. 5959-5973 ◽  
Author(s):  
N. Ma ◽  
C. S. Zhao ◽  
A. Nowak ◽  
T. Müller ◽  
S. Pfeifer ◽  
...  

Abstract. The largest uncertainty in the estimation of climate forcing stems from atmospheric aerosols. In early spring and summer of 2009, two periods of in-situ measurements on aerosol physical and chemical properties were conducted within the HaChi (Haze in China) project at Wuqing, a town between Beijing and Tianjin in the North China Plain (NCP). Aerosol optical properties, including the scattering coefficient (σsp), the hemispheric back scattering coefficient (σbsp), the absorption coefficient (σap), as well as the single scattering albedo (ω), are presented. The diurnal and seasonal variations are analyzed together with meteorology and satellite data. The mean values of σsp, 550 nm of the dry aerosol in spring and summer are 280±253 and 379±251 Mm−1, respectively. The average σap for the two periods is respectively 47±38 and 43±27 Mm−1. The mean values of ω at the wavelength of 637 nm are 0.82±0.05 and 0.86±0.05 for spring and summer, respectively. The relative high levels of σsp and σbsp are representative of the regional aerosol pollution in the NCP. Pronounced diurnal cycle of $σsp, σap and ω are found, mainly influenced by the evolution of boundary layer and the accumulation of local emissions during nighttime. The pollutants transported from the southwest of the NCP are more significant than that from the two megacities, Beijing and Tianjin, in both spring and summer. An optical closure experiment is conducted to better understand the uncertainties of the measurements. Good correlations (R>0.98) are found between the values measured by the nephelometer and the values calculated with a modified Mie model. The Monte Carlo simulation shows an uncertainty of about 30 % for the calculations. Considering all possible uncertainties of measurements, calculated σsp and σbsp agree well with the measured values, indicating a stable performance of instruments and thus reliable aerosol optical data.


2018 ◽  
Author(s):  
Fei Wang ◽  
Zhanqing Li ◽  
Xinrong Ren ◽  
Qi Jiang ◽  
Hao He ◽  
...  

Abstract. Vertical distributions of aerosol optical properties derived from measurements made during 11 aircraft flights over the North China Plain (NCP) in May–June 2016 during the Air Chemistry Research In Asia (ARIAs) were analyzed. Aerosol optical data from in situ aircraft measurements shows good correlation with ground-based measurements. The regional variability of aerosol optical profiles such as aerosol scattering and backscattering, absorption, extinction, single scattering albedo (SSA), and the Ångström exponent (α) are for the first time thoroughly characterized over the NCP. The SSA at 550 nm showed a regional mean value of 0.85 ± 0.02 with moderate to strong absorption and the α ranged from 0.49 to 2.53 (median 1.53) indicating both mineral dust and accumulation mode aerosols. Most of the aerosol particles were located in the lowest 2 km of the atmosphere. We describe three typical planetary boundary layer (PBL) scenarios and associated transport pathways as well as the correlation between aerosol scattering coefficients and relative humidity (RH). Aerosol scattering coefficients decreased slowly with height in the clean PBL condition, but decreased sharply above the PBL under polluted conditions, which showed a strong correlation (R2 ≥ 0.78) with ambient RH. Back-trajectory analysis shows that clean air masses generally originated from the distant north-western part of China while most of the polluted air masses were from the heavily polluted interior and coastal areas near the campaign area.


2018 ◽  
Vol 18 (12) ◽  
pp. 8995-9010 ◽  
Author(s):  
Fei Wang ◽  
Zhanqing Li ◽  
Xinrong Ren ◽  
Qi Jiang ◽  
Hao He ◽  
...  

Abstract. Vertical distributions of aerosol optical properties derived from measurements made during 11 aircraft flights over the North China Plain (NCP) in May–June 2016 during the Air Chemistry Research In Asia (ARIAs) were analyzed. Aerosol optical data from in situ aircraft measurements show good correlation with ground-based measurements. The regional variability of aerosol optical profiles such as aerosol scattering and backscattering, absorption, extinction, single scattering albedo (SSA), and the Ångström exponent (α) are thoroughly characterized for the first time over the NCP. The SSA at 550 nm showed a regional mean value of 0.85 ± 0.02 with moderate to strong absorption and the α ranged from 0.49 to 2.53 (median 1.53), indicating both mineral dust and accumulation-mode aerosols. Most of the aerosol particles were located in the lowest 2 km of the atmosphere. We describe three typical planetary boundary layer (PBL) scenarios and associated transport pathways as well as the correlation between aerosol scattering coefficients and relative humidity (RH). Aerosol scattering coefficients decreased slowly with height in the clean PBL condition, but decreased sharply above the PBL under polluted conditions, which showed a strong correlation (R2 ≥ 0.78) with ambient RH. Back-trajectory analysis shows that clean air masses generally originated from the distant northwestern part of China, while most of the polluted air masses were from the heavily polluted interior and coastal areas near the campaign region.


2011 ◽  
Vol 11 (11) ◽  
pp. 31137-31158 ◽  
Author(s):  
W. Y. Xu ◽  
C. S. Zhao ◽  
P. F. Liu ◽  
L. Ran ◽  
N. Ma ◽  
...  

Abstract. Emission information is crucial for air quality modelling and air quality management. In this study, a new approach based on the understanding of the relationship between emissions and measured pollutant concentrations has been proposed to estimate pollutant emissions and source contributions. The retrieval can be made with single point in-situ measurements combined with backward trajectory analyses. The method takes into consideration the effect of meteorology on pollutant transport when evaluating contributions and is independent of energy statistics, therefore can provide frequent updates on emission information. The spatial coverage can be further improved by using measurements from several sites and combining the derived emission fields. The method was applied to yield the source distributions of black carbon (BC) and CO in the North China Plain (NCP) using in-situ measurements from the HaChi (Haze in China) Campaign and to evaluate contributions from specific areas to local concentrations at the measurement site. Results show that this method can yield a reasonable emission field for the NCP and can directly quantify areal source contributions. Major BC and CO emission source regions are Beijing, the western part of Tianjin and Langfang, Hebei, with Tangshan being an additional important CO emission source area. The source contribution assessment suggests that, aside from local emissions in Wuqing, Tianjin and Hebei S, SW (d < 100 km) are the greatest contributors to measured local concentrations, while emissions from Beijing contribute little during summertime.


2020 ◽  
Author(s):  
Jiarui Wu ◽  
Naifang Bei ◽  
Yuan Wang ◽  
Xia Li ◽  
Suixin Liu ◽  
...  

Abstract. Accurate identification and quantitative source apportionment of fine particulate matters (PM2.5) provide an important prerequisite for design and implementation of emission control strategies to reduce PM pollution. Therefore, a source-oriented version of the WRF-Chem model is developed in the study to make source apportionment of PM2.5 in the North China Plain (NCP). A persistent and heavy haze event occurred in the NCP from 05 December 2015 to 04 January 2016 is simulated using the model as a case study to quantify PM2.5 contributions of local emissions and regional transport. Results show that local and non-local emissions contribute 36.3 % and 63.7 % of the PM2.5 mass in Beijing during the haze event on average. When Beijing's air quality is excellent or good in terms of hourly PM2.5 concentrations, local emissions dominate the PM2.5 mass with contributions exceeding 50 %. However, when the air quality is severely polluted, the PM2.5 contribution of non-local emissions is around 75 %. The non-local emissions also dominate the Tianjin's air quality, with average PM2.5 contributions exceeding 70 %. The PM2.5 level in Hebei and Shandong is generally controlled by local emissions, but in Henan, local and non-local emissions play an almost equivalent role in the PM2.5 level, except when the air quality is severely polluted, with non-local PM2.5 contributions of over 60 %. Additionally, the primary aerosol species are generally dominated by local emissions with the average contribution exceeding 50%. However, the source apportionment of secondary aerosols shows more evident regional characteristics. Therefore, except cooperation with neighboring provinces to carry out strict emission mitigation measures, reducing primary aerosols constitutes the priority to alleviate PM pollution in the NCP, especially in Beijing and Tianjin.


2019 ◽  
Vol 19 (20) ◽  
pp. 12857-12874 ◽  
Author(s):  
Renmin Yuan ◽  
Xiaoye Zhang ◽  
Hao Liu ◽  
Yu Gui ◽  
Bohao Shao ◽  
...  

Abstract. Due to excessive anthropogenic emissions, heavy aerosol pollution episodes (HPEs) often occur during winter in the Beijing–Tianjin–Hebei (BTH) area of the North China Plain. Extensive observational studies have been carried out to understand the causes of HPEs; however, few measurements of vertical aerosol fluxes exist, despite them being the key to understanding vertical aerosol mixing, specifically during weak turbulence stages in HPEs. In the winter of 2016 and the spring of 2017 aerosol vertical mass fluxes were measured by combining large aperture scintillometer (LAS) observations, surface PM2.5 and PM10 mass concentrations, and meteorological observations, including temperature, relative humidity (RH), and visibility, at a rural site in Gucheng (GC), Hebei Province, and an urban site at the Chinese Academy of Meteorological Sciences (CAMS) in Beijing located 100 km to the northeast. These are based on the light propagation theory and surface-layer similarity theory. The near-ground aerosol mass flux was generally lower in winter than in spring and weaker in rural GC than in urban Beijing. This finding provides direct observational evidence for a weakened turbulence intensity and low vertical aerosol fluxes in winter and polluted areas such as GC. The HPEs included a transport stage (TS), an accumulative stage (AS), and a removal stage (RS). During the HPEs from 25 to 31 January 2017, in Beijing, the mean mass flux decreased by 51 % from 0.0049 mg m−2 s−1 in RSs to 0.0024 mg m−2 s−1 in the TSs. During the ASs, the mean mass flux decreased further to 0.00087 mg m−2 s−1, accounting for approximately one-third of the flux in the TSs. A similar reduction from the TSs to ASs was observed in the HPE from 16 to 22 December 2016 in GC. It can be seen that from the TS to the AS, the aerosol vertical turbulent flux decreased, but the aerosol particle concentration within the surface layer increased, and it is inferred that in addition to the contribution of regional transport from upwind areas during the TS, suppression of vertical turbulence mixing confining aerosols to a shallow boundary layer increased accumulation.


2019 ◽  
Vol 53 (21) ◽  
pp. 12389-12397 ◽  
Author(s):  
Qiyuan Wang ◽  
Jianhuai Ye ◽  
Yichen Wang ◽  
Ting Zhang ◽  
Weikang Ran ◽  
...  

2020 ◽  
Vol ahead-of-print (ahead-of-print) ◽  
Author(s):  
Hongya Niu ◽  
Zhaoce Liu ◽  
Wei Hu ◽  
Wenjing Cheng ◽  
Mengren Li ◽  
...  

Purpose Severe airborne particulate pollution frequently occurs over the North China Plain (NCP) region in recent years. To better understand the characteristics of carbonaceous components in particulate matter (PM) over the NCP region. Design/methodology/approach PM samples were collected at a typical area affected by industrial emissions in Handan, in January 2016. The concentrations of organic carbon (OC) and elemental carbon (EC) in PM of different size ranges (i.e. PM2.5, PM10 and TSP) were measured. The concentrations of secondary organic carbon (SOC) were estimated by the EC tracer method. Findings The results show that the concentration of OC ranged from 14.9 μg m−3 to 108.4 μg m−3, and that of EC ranged from 4.0 μg m−3 to 19.4μg m−3, when PM2.5 changed from 58.0μg m−3 to 251.1μg m−3 during haze days, and the carbonaceous aerosols most distributed in PM2.5 rather than large fraction. The concentrations of OC and EC PM2.5 correlated better (r = 0.7) than in PM2.5−10 and PM>10, implying that primary emissions were dominant sources of OC and EC in PM2.5. The mean ratios of OC/EC in PM2.5, PM2.5–10 and PM>10 were 4.4 ± 2.1, 3.6 ± 0.9 and 1.9 ± 0.7, respectively. Based on estimation, SOC accounted for 16.3%, 22.0% and 9.1% in PM2.5, PM2.5–10 and PM>10 respectively. Originality/value The ratio of SOC/OC (48.2%) in PM2.5 was higher in Handan than those (28%–32%) in other megacities, e.g. Beijing, Tianjin and Shijiazhuang in the NCP, suggesting that the formation of SOC contributed significantly to OC. The mean mass absorption efficiencies of EC (MACEC) in PM10 and TSP were 3.4 m2 g−1 (1.9–6.6 m2 g−1) and 2.9 m2 g−1 (1.6–5.6 m2 g−1), respectively, both of which had similar variation patterns to those of OC/EC and SOC/OC.


2016 ◽  
Author(s):  
Yi Zhu ◽  
Jiping Zhang ◽  
Junxia Wang ◽  
Wenyuan Chen ◽  
Yiqun Han ◽  
...  

Abstract. The North China Plain (NCP) has been experiencing severe air pollution problems with rapid economic growth and urbanisation. Many field and model studies have examined the distribution of air pollutants in the NCP, but convincing results have not been achieved mainly due to a lack of direct measurements of pollutants over large areas. Here, we employed a mobile laboratory to observe the main air pollutants in a large part of the NCP from June 11 to July 15, 2013. High median concentrations of sulphur dioxide (SO2) (12 ppb), nitrogen oxides (NOx) (NO + NO2; 452 ppb), carbon monoxide (CO) (956 ppb), black carbon (BC; 5.5 μg m−3) and ultrafine particles (28 350 cm−3) were measured. Most of the high values, i.e., 95 percentile concentrations, were distributed near large cities, suggesting the influence of local emissions. In addition, we analysed the regional transport of SO2 and CO, relatively long-lived pollutants, based on our mobile observations together with wind field and satellite data analyses. Our results suggested that, for border areas of the NCP, wind from outside would have a diluting effect on pollutants, while south winds would bring in pollutants accumulated during transport through other parts of the NCP. For the central NCP, the concentrations of pollutants were likely to remain at high levels, partly due to the influence of regional transport by prevalent south–north winds over the NCP and partly by local emissions.


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