Research article 16 Sep 2021
Research article  16 Sep 2021
A new inverse modeling approach for emission sources based on the DDM3D and 3DVAR techniques: an application to air quality forecasts in the Beijing–Tianjin–Hebei region
 ^{1}State Key Lab of Severe Weather, Chinese Academy of Meteorological Sciences, Beijing 100081, China
 ^{2}Institute of Meteorology and Oceanography, National University of Defense Technology, Nanjing 211101, China
 ^{3}National Center for Atmospheric Research, Boulder, CO, USA
 ^{4}GZ Source Clear Tech. Co., Ltd., Guangzhou 510630, China
 ^{5}College of Architecture and Environment, Sichuan University, Chengdu 610065, China
 ^{6}Nanjing University of Information Science and Technology, Nanjing 210044, China
 ^{1}State Key Lab of Severe Weather, Chinese Academy of Meteorological Sciences, Beijing 100081, China
 ^{2}Institute of Meteorology and Oceanography, National University of Defense Technology, Nanjing 211101, China
 ^{3}National Center for Atmospheric Research, Boulder, CO, USA
 ^{4}GZ Source Clear Tech. Co., Ltd., Guangzhou 510630, China
 ^{5}College of Architecture and Environment, Sichuan University, Chengdu 610065, China
 ^{6}Nanjing University of Information Science and Technology, Nanjing 210044, China
Correspondence: Xinghong Cheng (cxingh@cma.gov.cn) and Zengliang Zang (zzlqxxy@163.com)
Hide author detailsCorrespondence: Xinghong Cheng (cxingh@cma.gov.cn) and Zengliang Zang (zzlqxxy@163.com)
We develop a new inversion method which is suitable for linear and nonlinear emission source (ES) modeling, based on the threedimensional decoupled direct (DDM3D) sensitivity analysis module in the Community Multiscale Air Quality (CMAQ) model and the threedimensional variational (3DVAR) data assimilation technique. We established the explicit observation operator matrix between the ES and receptor concentrations and the background error covariance (BEC) matrix of the ES, which can reflect the impacts of uncertainties of the ES on assimilation. Then we constructed the inversion model of the ES by combining the sensitivity analysis with 3DVAR techniques. We performed the simulation experiment using the inversion model for a heavy haze case study in the Beijing–Tianjin–Hebei (BTH) region during 27–30 December 2016. Results show that the spatial distribution of sensitivities of SO_{2} and NO_{x} ESs to their concentrations, as well as the BEC matrix of ES, is reasonable. Using an a posteriori inversed ES, underestimations of SO_{2} and NO_{2} during the heavy haze period are remarkably improved, especially for NO_{2}. Spatial distributions of SO_{2} and NO_{2} concentrations simulated by the constrained ES were more accurate compared with an a priori ES in the BTH region. The temporal variations in regionally averaged SO_{2}, NO_{2}, and O_{3} modeled concentrations using an a posteriori inversed ES are consistent with in situ observations at 45 stations over the BTH region, and simulation errors decrease significantly. These results are of great significance for studies on the formation mechanism of heavy haze, the reduction of uncertainties of the ES and its dynamic updating, and the provision of accurate “virtual” emission inventories for airquality forecasts and decisionmaking services for optimization control of air pollution.
Since the implementation of the Air Pollution Prevention and Control Action Plan in September 2013, urban air quality in China has improved overall. However, heavy haze frequently occurs over Beijing–Tianjin–Hebei (BTH) and the surrounding region in winter. In recent years, many researchers have studied the formation mechanism of heavy haze in the BTH region (Huang et al., 2014; Cheng et al., 2016; Liu et al., 2016). These studies have shown that rapid conversion from primary gas pollutants to particulates is an internal triggering factor for the “explosive” and “persistent” heavy haze (Wang et al., 2014), and secondary particulate concentrations, such as sulfate and nitrate, account for a significant percentage of PM_{2.5}. Thus, effectively controlling the emissions of precursors of secondary aerosols (such as SO_{2} and NO_{x}) is important for reducing environmental, economic, and human health problems caused by PM_{2.5} concentrations (Huang et al., 2014).
Emission inventories provide important fundamental data are crucial input data for investigating the causes of air pollution and for atmospheric chemical transport models (ACTMs). Uncertainties in the emission source (ES) are a major factor in determining the simulated and forecast accuracy of ACTMs, and these uncertainties can greatly affect the design of ES control strategies (Tang et al., 2006). The methods for establishing an emission inventory include the bottomup approach based on human activities, energy consumption statistics, and various emission factors, as well as topdown inversion modeling of the ES based on monitoring data of air pollutants using satellite remote sensing and ground observations. Many studies have established various ES inventories in China using the bottomup approach (e.g., Bai and Zhou, 1996; Streets et al., 2003; Zhang et al., 2009, 2012; Cao et al., 2011; Zhao et al., 2012, 2015; Li et al., 2017). However, the ES estimated by this method differ greatly due to large uncertainties in the statistical data, emission factors, and spatiotemporal apportionment coefficients (Ma and Van Aardenne, 2004). Moreover, realtime updates of emission inventories are difficult to achieve because of their rapid spatiotemporal variations due to highspeed urbanization and a delay in the release of statistical data of approximately 1–2 years. The topdown approach is a useful supplement to bottomup estimates, which are subject to uncertainties in emissions factors and activities (Streets et al., 2003). Inverse modeling, in which emissions are optimized to reduce the differences between simulated and observed data, is a powerful method that eliminates the problems of the bottomup approach.
Over the past decade, many researchers have tried to find an ideal inversion modeling tool that improves the spatiotemporal distribution of ES. With the development of data assimilation technology and ACTMs, constraining the strength of the ES using ACTMs has become one of the main topdown inversion methods (Enting, 2002; Sportisse, 2007). Researchers have primarily constrained the ES of weak active chemical pollutants, such as NO_{x}, CO, CO_{2}, SO_{2}, CH_{4}, and CHOCHO using the following methods: mass balance (Martin et al., 2003; Wang et al., 2007; Yang et al., 2011), backtrajectory inverse modeling (Manning et al., 2011), adjoint modeling (Liu et al., 2005; Koohkan et al., 2013; L. Zhang et al., 2016; Wang et al., 2018), Bayes estimation theory (Kopacz et al., 2009; Lucas et al., 2017), ensemble Kalman filtering (EnKF; Zhu and Wang, 2006; Zhu et al., 2018; Barbu et al., 2009; Tang et al., 2011, 2016; Miyazaki et al., 2012; Mijling and van der A, 2012; Wang et al., 2016; Peng et al., 2017; Chen et al., 2019; Dai et al., 2021), the fourdimension variational (4DVAR) technique (Elbern et al., 2000, 2007; Gilliland et al., 2006; Napelenok et al., 2008; Henze et al., 2009; Stavrakou et al., 2009; Corazza et al., 2011; Jiang et al., 2011), and an adaptive nudging scheme in the Community Multiscale Air Quality (CMAQ) model (Xu et al., 2008; Cheng et al., 2010). Results show that using an inversion modeling approach to retrieve the spatial distribution of ES can greatly improve air quality simulations and forecasts by the ACTM. Many studies have achieved a certain amount of improvement using the EnKF and 4DVAR methods. The advantage of the EnKF method is that the observation operator is implicit in the assimilation process of ES, and it avoids developing the tangent linear and adjoint models. For example, the fully coupled online Weather Research and Forecasting model coupled with Chemistry (WRFChem) is used as the forward model to relate the SO_{2} emissions to the simulated concentration and efficiently update the emissions based on routine surface SO_{2} observations (Dai et al., 2021). However, this method has stricter requirements for error perturbations in ES and the construction of biascorrection models. In addition, the large number of ensemble members in the EnKF method leads to a huge computational cost. Some studies adopted the 4DVAR method to inverse the ES of NO_{x} and CO based on the Goddard Earth Observing System (GEOS)Chem adjoint model. However, the GEOSChem model is often used to simulate largescale physical and chemical processes and is rarely utilized in urban air quality forecasts because its spatial resolution is too coarse. This method also has high computational costs due to the gradient calculation of the objective function.
The 3DVAR method is a generalization of optimal interpolation methods. It has the advantages of conveniently adding dynamical constraints and directly assimilating unconventional observation data (Li et al., 2013). 3DVAR is widely used in the assimilation of meteorological and atmospheric chemical data due to its simplicity, ability to use complex observations operators, and low computational cost. However, this method has two requirements: assimilated variables must remain relatively stationary within the assimilation window, and the method must be coordinated between the assimilated initial field and the iterative integration of the model. To apply the 3DVAR method to inverse the ES, it is necessary to construct an inversion model that can satisfy the aforementioned requirements. Firstly, although the ES have monthly, seasonal, and annual variations, the variation of ES is constant within a short period (e.g., for an assimilation window of 1 h). Secondly, the assimilation effect of the ES depends on the quality of observation data and the consistency between observed and simulated values. To ensure consistency between observations and simulations, the sensitivity of the receptor's concentrations with respect to the ES should be accurately calculated (Hu et al., 2009). Using the threedimensional decoupled direct (DDM3D) sensitivity analysis method within the CMAQ model, reasonable sensitivity coefficients between the ES and the receptor's concentrations can be calculated. This coefficient matrix is then used in the 3DVAR assimilation process, which ensures consistency between the ES and the modeled results. Thus, the topdown 3DVAR constraint methods for the ES based on the first or highorder DDM3D sensitivity analysis techniques can maintain the coordination between the assimilated field of the ES and the simulated concentration of air pollutants.
The primary methods used to calculate the S–R (source–receptor) relationship include the brute force, the adjoint, and the DDM3D method. Many studies have shown that these methods can improve ES inventories constructed by bottomup methods for NO_{x} (Napelenok et al., 2008), CO (Bergamaschi et al., 2000; Heald et al., 2004), NH_{3} (Gilliland et al., 2003), and elemental carbon (EC; Hu et al., 2009). The adjoint method is a backwardsensitivity calculation method, while brute force and DDM3D are forwardsensitivity calculation methods. For the inverse modeling of pollution sources with a single receptor, the backwardsensitivity method is more suitable, with low computation costs for certain grid sizes in a given time period, but it is not suitable for ES with multiple receptors, which result in high computational costs (Hu et al., 2009; Wang et al., 2013). The forwardsensitivity calculation method is more suitable for inversing the ES based on observed data from satellites or multiple surface stations (Hu et al., 2009). Cohan et al. (2002) introduced the DDM3D method to the CMAQ model and created the CMAQDDM3D module for loworder sensitivity calculations in early 2010. In 2014, they added a highorder calculation module for particles (HighOrder DDM3D for Particular Matter; HDDM3D/PM) in the newly released version of the CMAQ model. Wang et al. (2013) claim that the sensitivity calculation results using the DDM3D method are more reasonable than the brute force method. Some studies have used the DDM3D method (Napelenok et al., 2008; Hu et al., 2009) or a combination of the DDM3D and a discrete Kalman filter method (Wang et al., 2013) in conjunction with measurements from satellite and ground observations to inverse BC and NO_{x} ES in the United States. Because inverse modeling of ES based on discrete Kalman filtering is more suitable for linear systems, we use the DDM3D method to calculate the S–R linear and nonlinear relationship.
The results of inverse modeling are very sensitive to uncertainties in the ESs of NO_{x}, NH_{4}, and inorganic aerosols (L. Zhang et al., 2016). The impact of uncertainties in the ES on the assimilation effects needs to be considered in the topdown inversion model. The topdown 3DVAR inversion methods developed in this study can include the impacts of ES uncertainties by the background error covariance (BEC) matrix of the ES based on multiple sets of ESs. We developed a new inverse modeling approach for the ES that combines the DDM3D sensitivity analysis method with the 3DVAR assimilation technique and then applied it to a case study during a typical heavy haze episode. This paper is organized as follows: Sect. 2 describes the inversion model and presents results of the sensitivity analysis and the BEC; Sect. 3 provides details of the WRFCMAQ model and configurations and experiments of the simulation; Sect. 4 presents the results of the control and experiment simulations with a priori and a constrained posteriori ES, respectively; finally, the discussions and conclusions are provided in Sect. 5.
We used an offline modeling system that includes two components: the Weather Research and Forecasting (WRF) model (Michalakes et al., 2004) and the CMAQ model (Dennis et al., 1996; hereafter referred to as WRFCMAQ). This study focuses on the BTH region with 5×5 km grid spacing, 32 vertical layers of varying thickness (between the surface and 50 hPa), and an output interval of 1 h. The WRFCMAQ simulations are driven by the National Center for Environmental Prediction Final (NCEP FNL) analysis data every 6 h during 27–30 December 2016 and the Multiresolution Emission Inventory for China (MEIC) data for 2012, with $\mathrm{1}{}^{\circ}\times \mathrm{1}{}^{\circ}$ and $\mathrm{0.25}{}^{\circ}\times \mathrm{0.25}{}^{\circ}$ grid spacing, respectively. The CMAQ model was configured to utilize all layers from the input meteorology. Emissions datasets for CMAQ were generated by the Sparse Matrix Operator Kernel Emissions (SMOKE) model developed by the University of North Carolina (UNC, 2014). Meteorological outputs from the WRF simulations were processed to create modelready input to CMAQ using the MeteorologyChemistry Interface Processor (MCIP; Otte and Pleim, 2010). The boundary conditions for chemical trace gases consisted of idealized, northern hemispheric, midlatitude profiles based upon output from the National Oceanic Atmospheric Administration (NOAA) Agronomy Lab Regional Oxidant model. The model simulation started on 27 December 2016. To assess the improved effects of inverse modeling of ES during the heavy haze episode in December 2016, we ran two simulations: a control run with a priori MEIC data for 2012 and an experiment run with constrained a posteriori ES.
Hourly measurements of SO_{2}, NO_{2}, and O_{3} concentrations at 129 stations during 27–30 December 2016 were obtained from the China National Environmental Monitoring Centre. These data are used to validate simulations from the control and experiment runs. The simulation domains and the locations of the 129 stations are shown in Fig. 1.
3.1 Constructing the BEC matrix
To construct the BEC matrix for the inversion model, we combined the technique by the National Meteorological Center (NMC) (Parrish and Derber, 1992) with the SMOKE model based on uncertainty analysis of the ES inventories. We created the BEC matrix by four steps, as follows:

Determine the total errors of ES from an a priori bottomup inventory. Uncertainty analyses of ESs require detailed information of activities and emission factors from an a priori MEIC emission inventory. The relevant data collected in the China Environmental Yearbook are limited and do not satisfy the requirements of uncertainty analysis. Therefore, we used the available research results relating to SO_{2} and NO_{x} ESs and conducted uncertainty analysis for four types of major sources (industry, power plants, residents, and transportation) based on activities and emission factors from the references (Hong et al., 2017; Zheng et al., 2018; Peng et al., 2019) using the AuvTool software (Frey et al., 2002) and determined the error ranges in total emission rates of SO_{2} and NO_{x} (Table 1). Uncertainties in SO_{2} industry and power plant ESs are slightly greater than those for NO_{x}, while the opposite is true for emissions from the residential and traffic sectors.

Generate multiple sets of inventories using the random perturbation technique. Based on the aforementioned error ranges in total emission rates, we generated 30 sets of inventories for SO_{2} and NO_{x} with the same resolution as MEIC for each month using a random perturbation method (Kerry et al., 2007). Firstly we obtain the probability distribution of errors of ESs based on uncertainty analysis for four sections, respectively. Then we conduct random perturbation on uncertainties of four sections of ES 30 times according to the probability distributions using the same perturbation coefficients for every perturbation. Lastly we calculate 30 total emission rates using random uncertainties of four sections for every set of inventories, respectively.

Process the 3D gridded ES as input to the CMAQ model. We used the SMOKE model, national population and road network distribution data in 2016, the temporal apportionment coefficients in the BTH region (Zhang et al., 2007; Wang et al., 2008), and the CB05ae06aq chemical species data in the CMAQ model, to process 30 sets of nationwide emission inventories into 3D gridded ES with a grid spacing of 5×5 km. Each grid has 124×130 points, with 12 vertical levels.

Calculate the BEC matrix of each 3D gridded ES. Finally, the NMC method was used to calculate the BEC matrix of the 3D gridded ES for each month, including horizontal and vertical correlation coefficients and standard deviations. The background error is defined as the difference between 30 sets of 3D gridded ESs generated by the random perturbation method and the 3D gridded background ES directly processed from the original MEIC emission inventory with the SMOKE model, at every hour (24 h diurnal variation of ES for every month).
According to the literature (Liu et al., 2011; Li et al., 2013; Zang et al., 2016), the approximate calculation of the BEC matrix is as follows:
where e_{t} is the perturbation field, and e_{b} is the background field of an a priori ES. Equation (1) can be written as follows:
where D is the standard deviation (SD) matrix, and C is the correlation coefficient matrix. With this factorization, D and C can be calculated separately. D is a diagonal matrix, whose elements are the SD of all state variables in the 3D grids. C is used to improve the ability of the 3DVAR in representing the impacts of local emissions at one grid on other grids; these impacts vary in the vertical direction, and they are heterogeneous in the horizontal direction.
Figure 2 shows the spatial distribution of averaged emission rates for 30 sets of 3D gridded ESs and the SD of the BEC matrix for SO_{2} and NO_{x} ESs at 08:00 local time in December. SO_{2} and NO_{x} ESs have different spatial distributions in terms of average strength and standard deviation. The NO_{x} emissions are mainly concentrated in cities and surrounding areas, and they are much greater in Beijing, Tianjin, and Shijiazhuang than other cities. The SO_{2} emissions are mainly concentrated in Shijiazhuang, Jinan, the north and east of Shanxi Province, and their surrounding areas. Figure 3 shows variations in the horizontal correlation coefficients by grid distance and the vertical distributions of the SD in B for SO_{2} and NO_{x} ESs in December 2012. The cross between the correlation curve and the ${e}^{\mathrm{1}/\mathrm{2}}$ line (dashed line) represents the horizontal length scale (L_{s}), and the L_{s} of the two species falls between five and six grid distances. Namely, the horizontal scale felt is approximately 25–30 km. The correlation coefficient of SO_{2} is slightly larger than that of NO_{2}. The difference in the correlation coefficients between SO_{2} and NO_{x} ESsincreases with grid distance, and this is related to the regional pollution characteristics of SO_{2}. The vertical distributions of the SDs in B for SO_{2} and NO_{x} ESs vary with height: the SDs of the SO_{2} ES are larger on the fourth and eighth model levels than on other levels, while for the NO_{x} ES, the SD on the first level is the largest, that on the eighth level take the second place, and the SDs on all other levels are smaller.
3.2 Sensitivity analysis
The sensitivity analysis module (DDM3D) in CMAQ solves a series of equations while simultaneously calculating pollutant concentrations. The local sensitivity of pollutant concentrations with respect to several specified parameters, such as the ES, initial and boundary conditions, and chemical reaction rates, can be calculated by the DDM3D method. The sensitivity equations about the ES are solved using the governing equations of the model, as follows (Hu et al., 2009):
where S is the sensitivity of the pollutant j to the parameter p_{j}, p_{j} is an a priori ES of the pollutant j, C is the concentration of the pollutant j, and ε_{j} is the perturbation coefficient of the ES. Theoretically, the DDM3D method truly captures the sensitivities of pollutant concentrations to ES, and results are more accurate than the brute force method, for the BTH region (Wang et al., 2013). In addition, the results of the DDM3D method are more accurate and efficient for highly nonlinear pollutants (such as O_{3} and PM_{2.5}) and small perturbations.
We used the WRFv3.7.1 and CMAQv5.0.2DDM3D models as well as 3D gridded a priori ES from MEIC in 2012 to calculate the sensitivity coefficients of SO_{2} and NO_{2} concentrations with respect to ESs during the heavy haze episode of 27–30 December 2016. Figure 4 shows the spatial distribution of 96 h averaged sensitivity coefficients for SO_{2} and NO_{2} concentrations with respect to ESs during 27–30 December 2016. The sensitivity coefficients of SO_{2} and NO_{2} concentrations all exhibit inhomogeneous distribution. The sensitivity coefficients are higher in Beijing, Shijiazhuang, Baoding, and surrounding regions; i.e., SO_{2} and NO_{2} concentrations in those areas are greatly affected by the SO_{2} and NO_{x} ESs.
3.3 Observation operators
The relationship between pollutant source and the receptor's concentration is established according to Eq. (3). Next, we create the observation operator matrix between the ES and receptor concentrations as follows:
where H is the observation operator matrix, E denotes an a posteriori ES, which can be written as the product of the perturbation coefficient and an a priori ES during the assimilation window time, and E_{0} denotes an a priori ES. For primary pollutants such as SO_{2} and NO_{2}, S is a firstorder sensitivity coefficient, and H is a linear observation operator between the ES and the receptor concentration. For secondary pollutants such as PM_{2.5} and O_{3}, S is a highorder sensitivity coefficient, and H is a nonlinear observation operator. In this study, we use the firstorder sensitivity coefficient to calculate H for SO_{2} and NO_{x} ESs.
3.4 Observational error covariance
We firstly performed quality control on the observed SO_{2} and NO_{2} concentration data. This process involved three steps:

Redundant data were removed, and the density of observation data was matched to the model grid. For some grids with more than one observation station, we used the average of those stations.

Extrema were controlled; i.e., data exceeding 3 times the SD of observation data were filtered out.

Anomalies were removed; i.e., data that remained constant for 24 consecutive hours, as well as any negative data, were removed.
Data that passed quality control still contained observation or instrument errors. These errors are related to many factors such as instrument type, calibration design, and environmental conditions. In addition, in the variational assimilation process, representation errors caused by the forwardcalculation and variational processes must be considered. Higher resolution models produce smaller representation errors. Representation error, ε_{r}, can be expressed as follows (Pagowski et al., 2010):
where γ is the amplification factor, which is used to adjust the instrument error, ε_{o} is related to the SO_{2} and NO_{2} concentrations, and Δx is grid distance of the model. Note that L_{s} is usually smaller in urban areas and larger in suburban areas. The amplification parameters of the observing stations in cities, suburbs, and rural areas are 2.5, 5, and 10 km, respectively (Zang et al., 2016). Finally, the total observation error for the SO_{2} and NO_{2} concentrations, ε, is written as
3.5 3DVAR inversion model
We introduce a cost function with respect to the ES in accordance with 3DVAR:
where c is the observation variable, R is the observation error matrix, and e is the inversing variable of an a posteriori ES. The optimal inversion of the ES for SO_{2} and NO_{x} is obtained using Eq. (7). The 3DVAR solves for the minimum value of J(e) to determine the inversing variable e. This process typically employs a gradient propagation method, with the increment of an ES defined as follows:
Accordingly, the innovation vector of pollutant concentration is defined as
Therefore, Eq. (7) can be written in gradient form:
After conditionally processing the cost function, a finitememory quasiNewton method was used to conduct iterative minimization. The background field was set as the initial iteration values. The maximum number of steps at the end of the iteration and the minimum gradient for convergence were predetermined. The iteration was finished when one of these conditions was met, and the optimal analysis increment, δe, was obtained. Finally, the optimal assimilation analysis field of the ES, $\mathit{e}=\mathit{\delta}\mathit{e}+{\mathit{e}}_{\mathrm{b}}$, was obtained. The result was a threedimensional variational inversion model of the ES, using the uncertainty analysis of the ES and sensitivity coefficients between the ES and the receptor's concentrations; the overall framework is shown in Fig. 5.
A typical heavy haze event occurred in the BTH region at the end of December 2016. We applied the 3DVAR inversion model to constrain an hourly a posteriori ES of SO_{2} and NO_{2} using measurements from 45 and 129 stations, respectively, on 27 December 2016. We validated simulations from the control and experiment run using observational data during 28–30 December 2016.
Figure 6 shows time series of hourly, regional averaged SO_{2} and NO_{2} simulations from the control run, observations, and sensitivity coefficients at 45 stations in the BTH region during 27–30 December 2016. The trends in modeled concentrations and sensitivity coefficients of SO_{2} and NO_{2} concentrations with respect to the ES are consistent; therefore the sensitivity coefficients can reasonably reflect the impacts of the ES on concentrations. However, simulated SO_{2} and NO_{2} concentrations with an underestimated a priori ES are all significantly lower than observations during the heavy haze period. Thus, it is important to improve a priori ES using the inversion model.
Figures 7 and 8 show the spatial distributions of 24 h averaged emission rates from an a priori and a posteriori ES of SO_{2} and NO_{2} and their increments on 27 December 2016. Emission rates of a posteriori ES of SO_{2} and NO_{2} in the major cities and surrounding areas clearly increase. Compared with a priori ES, the maximum strengths of SO_{2} and NO_{2} ESs increase by approximately 17 % and 500 %, respectively. Therefore, the strengths of SO_{2} and NO_{2} in a priori ESs were greatly underestimated, especially for NO_{2}.
Using the WRFCMAQ model and an a posteriori ES, we simulated concentrations of SO_{2}, NO_{2}, and O_{3} in the BTH region during 28–30 December 2016 and validated these simulations with measurements from 45 stations. Figures 9 and 10 show the spatial distributions of 72 h averaged SO_{2} and NO_{2} concentrations simulated with a priori and a posteriori ESs, increments, and their observations. In general, SO_{2} and NO_{2} concentrations simulated using an a posteriori ES are closer to observations than an a priori ES, and regional differences in improvements for SO_{2} and NO_{2} exist. For SO_{2}, the improvement is noticeable in the BTH region. However, the simulated concentrations in Beijing with an a posteriori ES are overestimated. This may be related to greater uncertainties in SO_{2} sources and the impacts of regional transport from surrounding areas. For NO_{2}, simulated differences with a priori and a posteriori ESs are significant in major cities such as Beijing, Tianjin, Shijiazhuang, Baoding, Xingtai, Handan, and Jinan. The simulated concentrations of NO_{2} using a posteriori ES are more consistent with measurements, while those with a priori ES are significantly underestimated.
We also investigated temporal variations in regionally averaged SO_{2}, NO_{2}, and O_{3} concentrations simulated using a priori and a posteriori ESs and observations from the 45 stations over the BTH region during 28–30 December 2016 (Fig. 11). In general, simulated SO_{2}, NO_{2}, and O_{3} concentrations using an a posteriori ES are closer to measurements, while the SO_{2} and NO_{2} concentrations simulated by an a priori ES are significantly lower than observations, and the modeled O_{3} concentrations are obviously higher than measurements. In addition, the peak of SO_{2} simulations with an a posteriori ES is close to measurements, but the peak of NO_{2} and valley of O_{3} simulations are lower and higher than observations, respectively. This may be related to the absence of inverse modeling of a volatile organic compound (VOC) ES and the uncertainties of sensitivity coefficients calculation. In this study, we used only firstorder sensitivity coefficients, but the relationship between the ES of precursors of O_{3} such as VOCs and NO_{x} and their receptor's concentrations is nonlinear, and O_{3} is generated from both the NO_{x} and VOC ES. Therefore, higher order sensitivity coefficients are necessary for the inverse modeling of the ES of NO_{x} and VOCs.
To further assess the simulated accuracy of SO_{2}, NO_{2}, and O_{3} concentrations, we calculated the following statistics (Willmott et al., 2012): correlation coefficient (R), rootmeansquared error (RMSE), mean bias (MB), normalized mean bias (NMB), and index of agreement (IOA; see Table 2). Except the result that R values of NO_{2} and O_{3} decrease and the RMSE of O_{3} increases using the constrained ES, other statistics show improvements. In particular, MB and NMB of three pollutants decline significantly, and IOA is closer to 1.0, which means that modeled results of the three pollutants are more consistent with observations. R between SO_{2} simulation and observation shows a slight improvement when using an a posteriori ES, whereas R decreases for NO_{2} and O_{3}, and it may be related with the absence of constraint of a VOC ES.
We developed a new inverse approach of ES by combining the sensitivity analysis technique between the ES and the receptor's concentration and the 3DVAR method. Our approach is suitable for solving the linear or nonlinear inversion problems for ESs It computes quickly and obtains relatively accurate realtime dynamic updates of ESs. First, we used the sensitivity analysis tool in the CMAQ model to construct the explicit observation operator matrix between the ES and the receptor's concentration. Next, we created the BEC matrix for ES based on uncertainty analysis and the NMC statistical method. Finally, we established a threedimensional variational inverse method of ES based on the observation operator and BEC matrix.
The 3DVAR inversion model was applied to a heavy haze case study in the BTH region during 27–30 December 2016. Results show that the observation operators between SO_{2} and NO_{2} ESs and their concentrations, as well as spatial distributions of the BEC matrix, are both reasonable. Using the 3DVAR inversion model, a priori SO_{2} and NO_{2} ESs improved obviously during the heavy haze process, especially for the NO_{2} ES. The spatial distributions of SO_{2} and NO_{2} concentrations simulated using an a posteriori ES are more consistent with measurements than an a priori ES, especially in major cities over the BTH region. Simulation errors of SO_{2}, NO_{2}, and O_{3} concentrations with an a posteriori ES significantly decrease, whereas simulations of three pollutants using an a priori ES are underestimated.
Large discrepancies of the simulation and sensitivity coefficient over December 29 may be related with absent calculation of highorder sensitivity coefficient in this case. In the future, we will adopt highorder sensitivity coefficient to improve the constraint effect of SO_{2} and NO_{x} emission sources. In addition, future studies will include the applicability and accuracy of this method for different seasons and regions and different chemical species such as other primary pollutants (e.g., CO) and precursors of secondary pollutants (e.g., PM_{2.5}, PM_{10}, and O_{3}). An emphasis may be placed on constructing the nonlinear explicit observation operator for precursors of secondary pollutants such as a VOC ES using the highorder sensitivity analysis technique and assessing improvement effects of an a posteriori ES with the 3DVAR inversion method and the CMAQ model.
The NCEPFNL reanalysis data are publicly available at https://doi.org/10.5065/D6M043C6 (National Center for Atmospheric Research, 2021). The SO_{2}, NO_{2}, and O_{3} measurements are available at http://www.cnemc.cn/en/ (last access: 8 September 2021, China National Environmental Monitoring Centre, 2013).
XC and ZZ designed the research. XC and ZH constructed the 3DVAR inversion model, designed model experiments, and performed simulations. XC, ZH, ZZ, YL, YH, and XM contributed to the data processing and analyses. XC and ZH analyzed the results and wrote the paper with inputs from all authors. ZL and XX contributed to the theoretical direction for establishing the inversion model. SW performed the uncertainty analysis of ES.
The contact author has declared that neither they nor their coauthors have any competing interests.
Publisher's note: Copernicus Publications remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Our thanks are due to Yongtao Hu from the Georgia Institute of Technology for assistance with the calculation of the sensitivity. We are grateful to Tsinghua University for providing the emission inventory and the China National Environmental Monitoring Centre for providing surface SO_{2}, NO_{2}, and O_{3} observation data.
This research has been jointly supported by the Fundamental Research Funds for Central Publicinterest Scientific Institution from the Chinese Academy of Meteorological Sciences (grant no. 2016Y005), the National Natural Science Foundation of China (grant no. 91644223), and the National Research Program for Key Issues in Air Pollution Control (grant no. DQGG0104).
This paper was edited by Qiang Zhang and reviewed by two anonymous referees.
Bai, N. B. and Zhou, X. J.: Estimation of CO_{2}, SO_{2} and NO_{x} gridded emission sources with a resolution of $\mathrm{1}{}^{\circ}\times \mathrm{1}{}^{\circ}$ in Changes of atmospheric ozone and its impact on climate and environment in China, China Meteorological Press, Beijing, 145–150, 1996.
Barbu, A. L., Segers, A. J., Schaap, M., Heemink, A. W., and Builtjes, P. J. H.: A multicomponent data assimilation experiment directed to sulphur dioxide and sulphate over Europe, Atmos. Environ., 43, 1622–1631, 2009.
Bergamaschi, P., Hein, R., Heimann, M., and Crutzen, M., P. J.: Inverse modeling of the global CO cycle: 1. Inversion of CO mixing ratios, J. Geophys. Res., 105, 1909–1927, 2000.
Cao, G. L., Zhang, X. Y., Gong, S. L., Gong, S. L., An, X. Q., and Wang, Y. Q.: Emission inventories of primary particles and pollutant gases for China, Chin. Sci. Bull., 56, 781, https://doi.org/10.1007/s1143401143737, 2011.
Cheng, X., Xu, X., and Ding, G.: An emission source inversion model based on satellite data and its application in air quality forecasts, Science China: Earth Sciences, 53, 752–762, 2010.
Cheng, Y. F., Zheng, G. J., Wei, C., Mu, Q., Zheng, B., Wang, Z. B, Gao, M., Zhang, Q., He, K. B., Carmichael, G., Pöschl, U., and Su, H.: Reactive nitrogen chemistry in aerosol water as a source of sulfate during haze events in China, Sci. Adv., 2, e1601530, https://doi.org/10.1126/sciadv.1601530, 2016.
Chen, D., Liu, Z., Ban, J., and Chen, M.: The 2015 and 2016 wintertime air pollution in China: SO_{2} emission changes derived from a WRFChem/EnKF coupled data assimilation system, Atmos. Chem. Phys., 19, 8619–8650, https://doi.org/10.5194/acp1986192019, 2019.
China National Environmental Monitoring Centre (CNEMC): SO_{2}, NO_{2}, and O_{3} measurements, CNEMC [data set], available at: http://www.cnemc.cn/en/ (last access: 8 September 2021), 2013.
Cohan, D., Hu, Y., Hakami, A., Odman, M. T., and Russell, A.: Implementation of a direct sensitivity method into CMAQ, Models3 User's Workshop, RTP, North Carolina, 22 October 2002.
Corazza, M., Bergamaschi, P., Vermeulen, A. T., Aalto, T., Haszpra, L., Meinhardt, F., O'Doherty, S., Thompson, R., Moncrieff, J., Popa, E., Steinbacher, M., Jordan, A., Dlugokencky, E., Brühl, C., Krol, M., and Dentener, F.: Inverse modelling of European N_{2}O emissions: assimilating observations from different networks, Atmos. Chem. Phys., 11, 2381–2398, https://doi.org/10.5194/acp1123812011, 2011.
Dai, T., Cheng, Y., Goto, D., Li, Y., Tang, X., Shi, G., and Nakajima, T.: Revealing the sulfur dioxide emission reductions in China by assimilating surface observations in WRFChem, Atmos. Chem. Phys., 21, 4357–4379, https://doi.org/10.5194/acp2143572021, 2021.
Dennis, R., Byun, D., and Novak, J.: The next generation of integrated air quality modeling: EPA's Models3, Atmos. Environ., 30, 1925–1938, 1996.
Elbern, H., Schmidt, H., Talagrand, O., and Ebel, A.: 4Dvariational data assimilation with an adjoint air quality model for emission analysis, Environ. Modell. Softw., 15, 539–548, 2000.
Elbern, H., Strunk, A., Schmidt, H., and Talagrand, O.: Emission rate and chemical state estimation by 4dimensional variational inversion, Atmos. Chem. Phys., 7, 3749–3769, https://doi.org/10.5194/acp737492007, 2007.
Enting, I. G.: Inverse Problems in Atmospheric Constituent Transport, Cambridge University Press, Cambridge, ISBN 9780521812108, 2002.
Frey, H. C., Zheng, J., Zhao, Y., Li, S., and Zhu, Y.: Technical Documentation of the AuvTool Software for Analysis of Variability and Uncertainty, North Carolina State University for the Office of Research and Development, U.S. Environmental Protection Agency, Research Triangle Park, NC, 2002.
Gilliland, A. B., Dennis, R. L., Roselle, S. J., and Pierce, T. E.: Seasonal NH_{3} emission estimates for the eastern United States based on ammonium wet concentrations and an inverse modeling method, J. Geophys. Res., 108, 4477, https://doi.org/10.1029/2002JD003063, 2003.
Gilliland, A. B., Wyat, A. K., Pinder, R. W., and Dennis, R. L.: Seasonal NH_{3} emissions for the continental united states: Inverse model estimation and evaluation, Atmos. Environ., 40, 4986–4998, 2006.
Heald, C. L., Jacob, D. J., Jones, D. B. A., Palmer, P. I., Logan, J. A., Streets, D. G., Sachse, G. W., Gille, J. C., Hoffman, R. N., and Nehrkorn, T.: Comparative inverse analysis of satellite (MOPITT) and aircraft (TRACEP) observations to estimate Asian sources of carbon monoxide, J. Geophys. Res., 109, D23306, https://doi.org/10.1029/2004JD005185, 2004.
Henze, D. K., Seinfeld, J. H., and Shindell, D. T.: Inverse modeling and mapping US air quality influences of inorganic PM_{2.5} precursor emissions using the adjoint of GEOSChem, Atmos. Chem. Phys., 9, 5877–5903, https://doi.org/10.5194/acp958772009, 2009.
Hong, C., Zhang, Q., He, K., Guan, D., Li, M., Liu, F., and Zheng, B.: Variations of China's emission estimates: response to uncertainties in energy statistics, Atmos. Chem. Phys., 17, 1227–1239, https://doi.org/10.5194/acp1712272017, 2017.
Hu, Y., Odman, M. T., and Russell, A. G.: Topdown analysis of the elemental carbon emissions inventory in the United States by inverse modeling using Community Multiscale Air Quality model with decoupled direct method (CMAQDDM), J. Geophys. Res., 114, D24302, https://doi.org/10.1029/2009JD011987, 2009.
Huang, R. J., Zhang, Y., Bozzetti, C., Ho, K. F., Cao, J. J., Han, Y., Daellenbach, K. R., Slowik, J. G., Platt, S. M., Canonaco, F., Zotter, P., Wolf, R., Pieber, S. M., Bruns, E. A., Crippa, M., Ciarelli, G., Piazzalunga, A., Schwikowski, M., Abbaszade, G., SchnelleKreis, J., Zimmermann, R., An, Z., Szidat, S., Baltensperger, U., Haddad, I. E., and Prévôt, A. S.: High secondary aerosol contribution to particulate pollution during haze events in China, Nature, 514, 218–222, 2014.
Jiang, Z., Jones, D. B. A., Kopacz, M., Liu, J., Henze, D. K., and Heald, C.: Quantifying the impact of model errors on topdown estimates of carbon monoxide emissions using satellite observations, J. Geophys. Res., 116, D15306, https://doi.org/10.1029/2010JD015282, 2011.
Kerry, A., Gerhard, R., and Mike, D. F.: Firegrowth modelling using meteorological data with random and systematic perturbations, Int. J. Wildland Fire, 16, 174–182, 2007.
Koohkan, M. R., Bocquet, M., Roustan, Y., Kim, Y., and Seigneur, C.: Estimation of volatile organic compound emissions for Europe using data assimilation, Atmos. Chem. Phys., 13, 5887–5905, https://doi.org/10.5194/acp1358872013, 2013.
Kopacz, M., Jacob, D. J., Henze, D. K., Heald, C. L., Streets, D. G., and Zhang, Q.: Comparison of adjoint and analytical Bayesian inversion methods for constraining Asian sources of carbon monoxide using satellite (MOPITT) measurements of CO columns, J. Geophys. Res., 114, D04305, https://doi.org/10.1029/2007JD009264, 2009.
Li, M., Liu, H., Geng, G., Hong, C., Liu, F., Song, Y., Tong, D., Zheng, B., Cui, H., Man, H., Zhang, Q., He, K.: Anthropogenic emission inventories in China: a review, Natl. Sci. Rev., 4, 834–866, 2017.
Li, Z., Zang, Z., Li, Q. B., Chao, Y., Chen, D., Ye, Z., Liu, Y., and Liou, K. N.: A threedimensional variational data assimilation system for multiple aerosol species with WRF/Chem and an application to PM_{2.5} prediction, Atmos. Chem. Phys., 13, 4265–4278, https://doi.org/10.5194/acp1342652013, 2013.
Liu, F., Hu, F., and Zhu, J.: Solving the optimal layout problem of multiple industrial pollution sources using the adjoint method, Science China: Earth Sciences, 35, 64–71, 2005.
Liu, J., Mauzerallb, D. L., Chen. Q., Zhang, Q., Song, Y., Peng, W., Klimont, Z., Qiu, X. H., Zhang, S. Q., Hu, M., Lin, W. L., Smith, K. R., and Zhu, T.: Air pollutant emissions from Chinese households: A major and underappreciated ambient pollution source, P. Natl. Acad. Sci. USA, 113, 7756–7761, 2016.
Liu, Z., Liu, Q., Lin, H. C., Schwartz, C. S., Lee, Y. H., and Wang, T.: Threedimensional variational assimilation of MODIS aerosol optical depth: implementation and application to a dust storm over East Asia, J. Geophys. Res., 116, D23206, https://doi.org/10.1029/2011JD016159, 2011.
Lucas, D. D., Simpson, M., CameronSmith, P., and Baskett, R. L.: Bayesian inverse modeling of the atmospheric transport and emissions of a controlled tracer release from a nuclear power plant, Atmos. Chem. Phys., 17, 13521–13543, https://doi.org/10.5194/acp17135212017, 2017.
Ma, J. and van Aardenne, J. A.: Impact of different emission inventories on simulated tropospheric ozone over China: a regional chemical transport model evaluation, Atmos. Chem. Phys., 4, 877–887, https://doi.org/10.5194/acp48772004, 2004.
Manning, A. J., Doherty, S. O., Jones, A. R., Simmonds, P. G., Derwent, R. G.: Estimating UK methane and nitrous oxide emissions from 1990 to 2007 using an inversion modeling approach, J. Geophys. Res., 116, D02305, https://doi.org/10.1029/2010JD014763, 2011.
Martin, R. V., Jacob, D. J., Chance, K., Palmer, P. I., and Evans, M. J.: Global inventory of nitrogen oxide emissions constrained by spacebased observations of NO_{2} columns, J. Geophys. Res., 108, 4537, https://doi.org/10.1029/2003JD003453, 2003.
Michalakes, J., Dudhia, J., Gill, D., Henderson, T., Klemp, J., Skamarock, W., and Wang, W.: The Weather Reseach and Forecast Model: Software Architecture and Performance, in: Proceedings of the 11th ECMWF Workshop on the Use of High Performance Computing In Meteorology, Reading, UK, edited by: Mozdzynski, G., 25–29 October 2004.
Mijling, B. and van der A, R. J.: Using daily satellite observations to estimate emissions of shortlived air pollutants on a mesoscopic scale, J. Geophys. Res., 117, D17302, https://doi.org/10.1029/2012JD017817, 2012.
Miyazaki, K., Eskes, H. J., and Sudo, K.: Global NO_{x} emission estimates derived from an assimilation of OMI tropospheric NO_{2} columns, Atmos. Chem. Phys., 12, 2263–2288, https://doi.org/10.5194/acp1222632012, 2012.
Napelenok, S. L., Pinder, R. W., Gilliland, A. B., and Martin, R. V.: A method for evaluating spatiallyresolved NOx emissions using Kalman filter inversion, direct sensitivities, and spacebased NO2 observations, Atmos. Chem. Phys., 8, 5603–5614, https://doi.org/10.5194/acp856032008, 2008.
National Center for Atmospheric Research: NCEP FNL Operational Model Global Tropospheric Analyses, continuing from July 1999, Research Data Archive at the National Center for Atmospheric Research, Computational and Information Systems Laboratory [data set], https://doi.org/10.5065/D6M043C6, 2021.
Otte, T. L. and Pleim, J. E.: The MeteorologyChemistry Interface Processor (MCIP) for the CMAQ modeling system: updates through MCIPv3.4.1, Geosci. Model Dev., 3, 243–256, https://doi.org/10.5194/gmd32432010, 2010.
Pagowski, M., Grell, G. A., McKeen, S. A., Peckham, S. E., and Devenyi, D.: Threedimensional variational data assimilation of ozone and fine particulate matter observations: some results using the weather research and forecastingchemistry model and gridpoint statistical interpolation, Q. J. Roy. Meteor. Soc., 136, 2013–2024, 2010.
Parrish, D. F. and Derber, J. C.: The National Meteorological Center's spectral statistical interpolation analysis scheme, Mon. Weather Rev., 120, 1747–1763, 1992.
Peng, L., Zhang, Q., Yao, Z., Mauzerall, D. L., Kang, S., Du, Z., Zheng, Y., Xue, T., and He, K.: Underreported coal in statistics: A surveybased solid fuel consumption and emission inventory for the rural residential sector in China, Appl. Energ., 235, 1169–1182, 2019.
Peng, Z., Liu, Z., Chen, D., and Ban, J.: Improving PM_{2.5} forecast over China by the joint adjustment of initial conditions and source emissions with an ensemble Kalman filter, Atmos. Chem. Phys., 17, 4837–4855, https://doi.org/10.5194/acp1748372017, 2017.
Sportisse, B.: A review of current issues in air pollution modeling and simulation, Computat. Geosci., 11, 159–181, 2007.
Stavrakou, T., Müller, J.F., De Smedt, I., Van Roozendael, M., Kanakidou, M., Vrekoussis, M., Wittrock, F., Richter, A., and Burrows, J. P.: The continental source of glyoxal estimated by the synergistic use of spaceborne measurements and inverse modelling, Atmos. Chem. Phys., 9, 8431–8446, https://doi.org/10.5194/acp984312009, 2009.
Streets, D. G., Bond, T. C., Carmichael, G. R., Fernandes, S. D., Fu, Q., He, D., Klimont, Z., Nelson, S. M., Tsai, N. Y., Wang, M. Q., Woo, J. H., and Yarber, K. F.: An inventory of gaseous and primary aerosol emissions in Asia in the year 2000, J. Geophys. Res., 108, 8809–8820, 2003.
Tang, X., Zhu, J., Wang, Z. F., and Gbaguidi, A.: Improvement of ozone forecast over Beijing based on ensemble Kalman filter with simultaneous adjustment of initial conditions and emissions, Atmos. Chem. Phys., 11, 12901–12916, https://doi.org/10.5194/acp11129012011, 2011.
Tang, X., Zhu, J., Wang, Z., Gbaguidi, A., Lin, C., Xin, J., Song, T., and Hu, B.: Limitations of ozone data assimilation with adjustment of NO_{x} emissions: mixed effects on NO_{2} forecasts over Beijing and surrounding areas, Atmos. Chem. Phys., 16, 6395–6405, https://doi.org/10.5194/acp1663952016, 2016.
Tang, X. Y., Zhang, Y. H., and Shao, M.: Atmospheric Environmental Chemistry, 2nd edn., Higher Education Press, Beijing, 447–449, 2006 (in Chinese).
The University of North Carolina (UNC): SMOKE v3.6 user's manual, The institute for the Environment, Chapel Hill, 520 pp., 2014.
Wang, C., An, X. Q., Zhai, S. X., Hou, Q., and Sun, Z. B.: Tracking sensitive source areas of different weather pollution types using GRAPESCUACE adjoint model, Atmos. Environ., 175, 154–166, 2018.
Wang, L. T., Zhang, P., Yang, J., Zhao, X. J., Wei, W., Su, J., Cheng, D. D., Liu X., Y., Han, G., G., and Wang, H. J.: Application of CMAQDDM3D in the source analysis of fine particulate matter (PM_{2.5}), Acta Scientiae Circumstantiae, 33, 1355–1361, 2013 (in Chinese).
Wang, P., Wang, H., Wang, Y. Q., Zhang, X. Y., Gong, S. L., Xue, M., Zhou, C. H., Liu, H. L., An, X. Q., Niu, T., and Cheng, Y. L.: Inverse modeling of black carbon emissions over China using ensemble data assimilation, Atmos. Chem. Phys., 16, 989–1002, https://doi.org/10.5194/acp169892016, 2016.
Wang, Y., McElroy, M. B., Martin, R. V., Streets, D. G., Zhang, Q., and Fu, T.M.: Seasonal variability of NO_{x} emissions over east China constrained by satellite observations: Implications for combustion and microbial sources, J. Geophys. Res., 112, D06301, https://doi.org/10.1029/2006JD007538, 2007.
Wang, Q., Huo, H., He, K., Yao, Z., and Zhang, Q.: Characterization of vehicle driving patterns and development of driving cycles in Chinese cities, Transport. Res. DTr. E., 13, 289–297, 2008.
Wang, Y. S., Yao, L., Wang, L., L., Liu, Z. R., Ji, D. S., Tang, G. Q., Zhang, J. K., Sun, Y., Hu, B., and Xin, J. Y.: Mechanism for the formation of the January 2013 heavy haze pollution episode over central and eastern China, Science China, Earth Sciences, 57, 14–25, 2014 (in Chinese).
Willmott, C. J., Robeson, S. M., and Matsuura, K. A.: A refined index of model performance, Int. J. Climatol., 32, 2088–2094, 2012.
Xu, X. D., Xie, L. A., Cheng, X. H., Xu., J. M., Zhou, X. J., and Ding, G. A.: Application of an Adaptive Nudging Scheme in Air Quality Forecasting in China, J. Appl. Meteorol. Climatol., 47, 2105–2114, 2008.
Yang, Q., Wang, Y. H., Zhao, C., Liu, Z., William, I., Gustafson, J., and Shao, M.: NO_{x} emission reduction and its effects on ozone during the 2008 Olympic Games, Environ. Sci. Technol., 45, 6404–6410, 2011.
Zang, Z. L., Li, Z. J., Pan, X. B., Hao, Z. L., and You, W.: Aerosol data assimilation and forecasting experiments using aircraft and surface observations during CalNex, Tellus B, 68, 29812, https://doi.org/10.3402/tellusb.v68.29812, 2016.
Zhang, Q., Streets, D. G., He, K., Wang, Y., Richter, A., Burrows, J. P., Uno, I., Jang, C. J., Chen, D., Yao, Z., and Lei Y.: NO_{x} emission trends for China, 1995–2004: The view from the ground and the view from space, J. Geophys. Res., 112, D22306, https://doi.org/10.1029/2007JD008684, 2007.
Zhang, L., Shao, J. Y., Lu, X., Zhao, Y. H., Hu, Y. Y., Henze, D., Liao, H., Gong, S., L., and Zhang, Q.: Sources and processes affecting fine particulate matter pollution over North China: An adjoint analysis of the Beijing APEC period, Environ. Sci. Technol., 50, 8731–8740, 2016.
Zhang, Q., Geng, G. N., Wang, S. W., Andreas, R., and He, K. B.: Satellite remote sensing of changes in NO_{x} emissions over China during 1996–2010, Chin. Sci. Bull., 57, 2857–2864, 2012.
Zhang, Q., Streets, D. G., Carmichael, G. R., He, K. B., Huo, H., Kannari, A., Klimont, Z., Park, I. S., Reddy, S., Fu, J. S., Chen, D., Duan, L., Lei, Y., Wang, L. T., and Yao, Z. L.: Asian emissions in 2006 for the NASA INTEXB mission, Atmos. Chem. Phys., 9, 5131–5153, https://doi.org/10.5194/acp951312009, 2009.
Zhao, B., Wang, P., Ma, J. Z., Zhu, S., Pozzer, A., and Li, W.: A highresolution emission inventory of primary pollutants for the Huabei region, China, Atmos. Chem. Phys., 12, 481–501, https://doi.org/10.5194/acp124812012, 2012.
Zhao, H. Y., Zhang, Q., Guan, D. B., Davis, S. J., Liu, Z., Huo, H., Lin, J. T., Liu, W. D., and He, K. B.: Assessment of China's virtual air pollution transport embodied in trade by using a consumptionbased emission inventory, Atmos. Chem. Phys., 15, 5443–5456, https://doi.org/10.5194/acp1554432015, 2015.
Zheng, B., Tong, D., Li, M., Liu, F., Hong, C., Geng, G., Li, H., Li, X., Peng, L., Qi, J., Yan, L., Zhang, Y., Zhao, H., Zheng, Y., He, K., and Zhang, Q.: Trends in China's anthropogenic emissions since 2010 as the consequence of clean air actions, Atmos. Chem. Phys., 18, 14095–14111, https://doi.org/10.5194/acp18140952018, 2018.
Zhu, J. and Wang, P.: Ensemble kalman smoother and ensemble kalman filter approaches to the joint air quality state and emission estimation problem, Chinese Journal of Atmospheric Sciences, 30, 871–882, 2006.
Zhu, J., Tang, X., Wang, Z. F., and Wu, L.: A review of air quality data assimilation methods and their application, Chinese Journal of Atmospheric Sciences, 42, 607–620, 2018.