scholarly journals Spatiotemporal Variations and Uncertainty in Crop Residue Burning Emissions over North China Plain: Implication for Atmospheric CO2 Simulation

2021 ◽  
Vol 13 (19) ◽  
pp. 3880
Author(s):  
Yu Fu ◽  
Hao Gao ◽  
Hong Liao ◽  
Xiangjun Tian
Keyword(s):  
Air Quality ◽  
Biomass Burning ◽  
Crop Residue ◽  
North China Plain ◽  
North China ◽  
Transport Model ◽  
Spatial Uncertainty ◽  
Burned Area ◽  
Crop Residue Burning ◽  
The Impact

Large uncertainty exists in the estimations of greenhouse gases and aerosol emissions from crop residue burning, which could be a key source of uncertainty in quantifying the impact of agricultural fire on regional air quality. In this study, we investigated the crop residue burning emissions and their uncertainty in North China Plain (NCP) using three widely used methods, including statistical-based, burned area-based, and fire radiative power-based methods. The impacts of biomass burning emissions on atmospheric carbon dioxide (CO2) were also examined by using a global chemical transport model (GEOS-Chem) simulation. The crop residue burning emissions were found to be high in June and followed by October, which is the harvest times for the main crops in NCP. The estimates of CO2 emission from crop residue burning exhibits large interannual variation from 2003 to 2019, with rapid growth from 2003 to 2012 and a remarkable decrease from 2013 to 2019, indicating the effects of air quality control plans in recent years. Through Monte Carlo simulation, the uncertainty of each estimation was quantified, ranging from 20% to 70% for CO2 emissions at the regional level. Concerning spatial uncertainty, it was found that the crop residue burning emissions were highly uncertain in small agricultural fire areas with the maximum changes of up to 140%. While in the areas with large agricultural fire, i.e., southern parts of NCP, the coefficient of variation mostly ranged from 30% to 100% at the gridded level. The changes in biomass burning emissions may lead to a change of surface CO2 concentration during the harvest times in NCP by more than 1.0 ppmv. The results of this study highlighted the significance of quantifying the uncertainty of biomass burning emissions in a modeling study, as the variations of crop residue burning emissions could affect the emission-driven increases in CO2 and air pollutants during summertime pollution events by a substantial fraction in this region.

scholarly journals Observation of atmospheric peroxides during Wangdu Campaign 2014 at a rural site in the North China Plain

2016 ◽  
Vol 16 (17) ◽  
pp. 10985-11000 ◽  
Author(s):  
Yin Wang ◽  
Zhongming Chen ◽  
Qinqin Wu ◽  
Hao Liang ◽  
Liubin Huang ◽  
...  
Keyword(s):  
Biomass Burning ◽  
North China Plain ◽  
North China ◽  
Chemical Mechanism ◽  
Rural Site ◽  
Direct Production ◽  
The North ◽  
The North China Plain ◽  
The Impact ◽  
Haze Days

Abstract. Measurements of atmospheric peroxides were made during Wangdu Campaign 2014 at Wangdu, a rural site in the North China Plain (NCP) in summer 2014. The predominant peroxides were detected to be hydrogen peroxide (H2O2), methyl hydroperoxide (MHP) and peroxyacetic acid (PAA). The observed H2O2 reached up to 11.3 ppbv, which was the highest value compared with previous observations in China at summer time. A box model simulation based on the Master Chemical Mechanism and constrained by the simultaneous observations of physical parameters and chemical species was performed to explore the chemical budget of atmospheric peroxides. Photochemical oxidation of alkenes was found to be the major secondary formation pathway of atmospheric peroxides, while contributions from alkanes and aromatics were of minor importance. The comparison of modeled and measured peroxide concentrations revealed an underestimation during biomass burning events and an overestimation on haze days, which were ascribed to the direct production of peroxides from biomass burning and the heterogeneous uptake of peroxides by aerosols, respectively. The strengths of the primary emissions from biomass burning were on the same order of the known secondary production rates of atmospheric peroxides during the biomass burning events. The heterogeneous process on aerosol particles was suggested to be the predominant sink for atmospheric peroxides. The atmospheric lifetime of peroxides on haze days in summer in the NCP was about 2–3 h, which is in good agreement with the laboratory studies. Further comprehensive investigations are necessary to better understand the impact of biomass burning and heterogeneous uptake on the concentration of peroxides in the atmosphere.

Assessment of the impact of emissions reductions on air quality over North China Plain

2016 ◽  
Vol 7 (2) ◽  
pp. 249-259 ◽  
Author(s):  
Xiao Han ◽  
Meigen Zhang ◽  
Lingyun Zhu ◽  
Andrei Skorokhod
Keyword(s):  
Air Quality ◽  
North China Plain ◽  
North China ◽  
Emissions Reductions ◽  
The Impact

scholarly journals Modeling Ozone Source Apportionment and Performing Sensitivity Analysis in Summer on the North China Plain

Atmosphere ◽  
2020 ◽  
Vol 11 (9) ◽  
pp. 992
Author(s):  
Yujing Zhang ◽  
Yuncheng Zhao ◽  
Jie Li ◽  
Qizhong Wu ◽  
Hui Wang ◽  
...  
Keyword(s):  
Air Quality ◽  
Source Apportionment ◽  
North China Plain ◽  
North China ◽  
Transport Model ◽  
Fine Particulate Matter ◽  
Hebei Province ◽  
Chemical Transport Model ◽  
The North ◽  
The North China Plain

In recent years, air quality issues due to fine particulate matter have been sufficiently treated. However, ozone (O3) has now become the primary pollutant in summer on the North China Plain (NCP). In this study, a three-dimensional chemical transport model (the Nested Air Quality Prediction Model System, NAQPMS) coupled with an online source apportionment module was applied to investigate the sources of O3 pollution over the NCP. Generally, the NAQPMS adequately captured the observed spatiotemporal features of O3 during the period of July 1st to August 31st in 2017 on the NCP. The results of the source apportionment indicated that the contributions of local emissions and transport from the NCP accounted for the largest proportion of O3, with magnitudes of 25% and 39%, respectively. Compared with those in the average monthly results, the local contribution and regional transport during O3 episodes on the NCP increased by 7% and 10%, respectively. Based on sensitivity tests, two thresholds of the sensitivity indicator P(H2O2)/P(HNO3) were detected, at 0.08 and 0.2. Ozone formation in the urban sites of Beijing, Tianjin, and the southern part of Hebei Province was controlled by VOCs, while the other sites were mainly controlled by NOX. Biogenic emissions contributed approximately 18% to O3 formation in July in the southwestern part of Hebei Province.

scholarly journals Intra-regional transport of black carbon between the south edge of North China Plain and Central China during winter haze episodes

2018 ◽  
Author(s):  
Huang Zheng ◽  
Shaofei Kong ◽  
Fangqi Wu ◽  
Yi Cheng ◽  
Zhenzhen Niu ◽  
...  
Keyword(s):  
Optical Properties ◽  
Air Quality ◽  
Biomass Burning ◽  
North China Plain ◽  
North China ◽  
Fossil Fuel ◽  
Central China ◽  
Geographic Origins ◽  
Regional Air Quality ◽  
Pollution Episodes

Abstract. Black carbon (BC), from the incomplete combustion sources (mainly fossil fuel, biofuel and open biomass burning), is chemically inertness and optical absorbance in the atmosphere. It has significant impacts on global climate, regional air quality, and human health. During the transportation, its physical-chemical characteristics, optical properties and sources would change dramatically. To investigate the BC properties (i.e., mass concentration, sources and optical properties) during the intra-regional transport between the south edge of North China Plain (SE-NCP) and Central China (CC), simultaneous observations of BC at a megacity (Wuhan, WH) in CC, three borderline cities (Xiangyang, XY, Suixian, SX and Hong'an, HA, distributing from the west to east) between SE-NCP and CC and a city (Luohe, LH) in SE-NCP were conducted during the typical winter haze episodes. Using Aethalometer, the highest equivalent BC (eBC) mass concentrations and aerosol absorption coefficients (σabs) were found in the city (LH) at SE-NCP, followed by the borderline cities (XY, SX and HA) and megacity (WH). The levels, sources, optical properties (i.e., σabs and absorption Ångström exponent, AAE) and geographic origins of eBC were different between clean and pollution episodes. Compared to clean days, the higher eBC levels (increased by 26.4–163 %) and σabs (increased by 18.2–236 %) were found during pollution episodes due to more combustion of fossil fuel (contributing for 51.1–277 %), supported by the decreased AAE (by 7.40–12.7 %). Non-parametric wind regression (NWR) and concentration-weighted trajectory (CWT) results showed that the geographic origins of biomass burning (BCbb) and fossil fuel (BCff) combustion derived BC were different. Based on cluster analysis of trajectories, air parcels from south direction dominated for border sites during clean days, with contributions of 46.0–58.2 %, while trajectories from the northeast had higher contributions (37.5–51.2 %) during pollution episodes. At the SE-NCP site (LH), transboundary influences from south direction (CC) exhibited more frequent impact (with the air parcels from this direction contributed 47.8 % of all the parcels) on the ambient eBC levels during pollution episodes. At WH, eBC was mainly from the northeast transport route during the whole observation period. Two transportation cases showed that from upwind to downwind direction, the mass concentrations of eBC, BCbb and BCff all increased, while AAE decreased. This study highlighted that intra-regional prevention and control for dominated sources of specific sites should be considered to improve the regional air quality.

scholarly journals Observation of atmospheric peroxides during Wangdu Campaign 2014 at a rural site in the North China Plain

2016 ◽  
Author(s):  
Yin Wang ◽  
Zhongming Chen ◽  
Qinqin Wu ◽  
Hao Liang ◽  
Liubin Huang ◽  
...  
Keyword(s):  
Biomass Burning ◽  
North China Plain ◽  
North China ◽  
Chemical Mechanism ◽  
Rural Site ◽  
Direct Production ◽  
The North ◽  
The North China Plain ◽  
The Impact ◽  
Haze Days

Abstract. Measurements of atmospheric peroxides were made during Wangdu Campaign 2014 at Wangdu, a rural site in the North China Plain (NCP) in summer 2014. The predominant peroxides were detected to be hydrogen peroxide (H2O2), methyl hydroperoxide (MHP) and peroxyacetic acid (PAA). The observed H2O2 reached up to 11.3 ppbv, which was the highest value compared with previous observations in China at summer time. A box model simulation based on the Master Chemical Mechanism and constrained by the simultaneous observations of physical parameters and chemical species was performed to explore the chemical budget of atmospheric peroxides. Photochemical oxidation of alkenes was found to be the major secondary formation pathway of atmospheric peroxides, while contributions from alkanes and aromatics were of minor importance. The comparison of modelled and measured peroxide concentrations revealed an underestimation during biomass burning events and an overestimation on haze days, which were ascribed to the direct production of peroxides from biomass burning and the heterogeneous uptake of peroxides by aerosols, respectively. The strengths of the primary emissions from biomass burning were on the same order of the known secondary production rates of atmospheric peroxides during the biomass burning events. The heterogeneous process on aerosol particles was suggested to be the predominant sink for atmospheric peroxides. The atmospheric lifetime of peroxides on haze days in summer in the NCP was about 2–3 hours, which is in good agreement with the laboratory studies. Further comprehensive investigations are necessary to better understand the impact of biomass burning and heterogeneous uptake on the concentration of peroxides in the atmosphere.

scholarly journals Crop Residue Burning in Northeast China and Its Impact on PM2.5 Concentrations in South Korea

Atmosphere ◽  
2021 ◽  
Vol 12 (9) ◽  
pp. 1212
Author(s):  
Jin-Ju Lee ◽  
Jae-Bum Lee ◽  
Okgil Kim ◽  
Gookyoung Heo ◽  
Hankyung Lee ◽  
...  
Keyword(s):  
Air Quality ◽  
South Korea ◽  
Northeast China ◽  
Crop Residue ◽  
Weather Conditions ◽  
Northeastern China ◽  
Thermal Anomalies ◽  
Crop Residue Burning ◽  
Satellite Analysis ◽  
The Impact

The impact of crop residue burning in northeastern China on South Korean PM2.5 concentrations was assessed via weather conditions, air quality modeling (AQM), and PM2.5 composition data during two cases exceeding 35 µg·m−3 in November 2015. PM2.5 concentration simulations of Case 1 differed from observations by 3.7–17.6 µg·m−3, overestimating the levels by 6–36%; however, Case 2 varied by 20.0–59.8 µg·m−3 from observations, with a 53–91% underestimation. Case 1 was generally well simulated, whereas the Case 2 simulation failed because the emissions of crop residue burning in northeastern China, as confirmed through satellite analysis (MODIS fires and thermal anomalies) and previous research, were not considered. The portion of organic/elemental carbon ratio during Case 2 was 1.6–2.3 times higher than that of Case 1. These results suggest that it is necessary to consider the effects of crop residue burning in northeast China to establish countermeasures to improve air quality and air quality forecasting in South Korea.

scholarly journals Size-resolved characterization of organic aerosol in the North China Plain: new insights from high resolution spectral analysis

2021 ◽  
Author(s):  
Weiqi Xu ◽  
Chun Chen ◽  
Yanmei Qiu ◽  
Conghui Xie ◽  
Yunle Chen ◽  
...  
Keyword(s):  
Radiative Forcing ◽  
North China Plain ◽  
North China ◽  
Fine Particles ◽  
Large Fraction ◽  
Organic Aerosol ◽  
Size Distributions ◽  
The North ◽  
The Impact

Organic aerosol (OA), a large fraction of fine particles, has a large impact on climate radiative forcing and human health, and the impact depends strongly on size distributions. Here we...

scholarly journals The Environmental Effects of the April 2020 Wildfires and the Cs-137 Re-Suspension in the Chernobyl Exclusion Zone: A Multi-Hazard Threat

Atmosphere ◽  
2021 ◽  
Vol 12 (4) ◽  
pp. 467
Author(s):  
Rocío Baró ◽  
Christian Maurer ◽  
Jerome Brioude ◽  
Delia Arnold ◽  
Marcus Hirtl
Keyword(s):  
Air Quality ◽  
Nuclear Power ◽  
Transport Model ◽  
Atmospheric Transport ◽  
Point Of View ◽  
Plume Dispersion ◽  
Exclusion Zone ◽  
Fire Plume ◽  
Mean Values ◽  
The Impact

This paper demonstrates the environmental impacts of the wildfires occurring at the beginning of April 2020 in and around the highly contaminated Chernobyl Exclusion Zone (CEZ). Due to the critical fire location, concerns arose about secondary radioactive contamination potentially spreading over Europe. The impact of the fire was assessed through the evaluation of fire plume dispersion and re-suspension of the radionuclide Cs-137, whereas, to assess the smoke plume effect, a WRF-Chem simulation was performed and compared to Tropospheric Monitoring Instrument (TROPOMI) satellite columns. The results show agreement of the simulated black carbon and carbon monoxide plumes with the plumes as observed by TROPOMI, where pollutants were also transported to Belarus. From an air quality and health perspective, the wildfires caused extremely bad air quality over Kiev, where the WRF-Chem model simulated mean values of PM2.5 up to 300 µg/m3 (during the first fire outbreak) over CEZ. The re-suspension of Cs-137 was assessed by a Bayesian inverse modelling approach using FLEXPART as the atmospheric transport model and Ukraine observations, yielding a total release of 600 ± 200 GBq. The increase in both smoke and Cs-137 emissions was only well correlated on the 9 April, likely related to a shift of the focus area of the fires. From a radiological point of view even the highest Cs-137 values (average measured or modelled air concentrations and modelled deposition) at the measurement site closest to the Chernobyl Nuclear Power Plant, i.e., Kiev, posed no health risk.

Sign in / Sign up

Export Citation Format

Share Document