Temporally resolved sectoral and regional contributions to air pollution in Beijing: informing short-term emission controls
- 1Lancaster Environment Centre, Lancaster University, Lancaster, United Kingdom
- 2School of Mathematics, University of Manchester, Manchester, United Kingdom
- 3State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing, China
- anow at: Campus Fryslân, University of Groningen, Leeuwarden, the Netherlands
- bnow at: College of Engineering, Mathematics and Physical Sciences, University of Exeter, Exeter, United Kingdom
Correspondence: Tabish Umar Ansari (email@example.com) and Oliver Wild (firstname.lastname@example.org)
We investigate the contributions of local and regional emission sources to air pollution in Beijing to inform the design of short-term emission control strategies for mitigating major pollution episodes. We use a well-evaluated version of the WRF-Chem model at 3 km horizontal resolution to determine the daily accumulation of pollution over Beijing from local and regional sources in October 2014 under a range of meteorological conditions. Considering feasible emission reductions across residential, transport, power, and industrial sectors, we find that 1 d controls on local emissions have an immediate effect on PM2.5 (particulate matter with diameter less than 2.5 µm) concentrations on the same day but can have lingering effects as much as 5 d later under stagnant conditions. One-day controls in surrounding provinces have the greatest effect in Beijing on the day following the controls but may have negligible effects under northwesterly winds when local emissions dominate. To explore the contribution of different emission sectors and regions, we perform simulations with each source removed in turn. We find that residential and industrial sectors from neighbouring provinces dominate PM2.5 levels in Beijing during major pollution episodes but that local residential emissions and industrial or residential emissions from more distant provinces can also contribute significantly during some episodes. We then perform a structured set of perturbed emission simulations to allow us to build statistical emulators that represent the relationships between emission sources and air pollution in Beijing over the period. We use these computationally fast emulators to determine the sensitivity of PM2.5 concentrations to different emission sources and the interactions between them, including for secondary PM, and to create pollutant response surfaces for daily average PM2.5 concentrations in Beijing. We use these surfaces to identify the short-term emission controls needed to meet the national air quality target of daily average PM2.5 less than 75 µg m−3 for pollution episodes of different intensities. We find that for heavily polluted days with daily mean PM2.5 higher than 225 µg m−3, even emission reductions of 90 % across all sectors over Beijing and surrounding provinces may be insufficient to meet the national air quality standards. These results highlight the regional nature of PM pollution and the challenges of tackling it during major pollution episodes.
Beijing, located at the foot of the Yan Mountains on the northern edge of the heavily populated North China Plain, has consistently been named among the most polluted capital cities in the world (State of Global Air, 2019; Global burden of disease, 2016). Key air pollutants including carbon monoxide, sulfur dioxide, nitrogen oxides, ozone, and PM2.5 (particulate matter with diameter less than 2.5 µm) often breach the World Health Organization (WHO) and national air quality standards, posing risks to human health, visibility, and climate (Lelieveld et al., 2015; Luan et al., 2018; United Nations Environment Programme and World Meteorological Organization, 2011). To address the severe ambient air pollution in Chinese cities, the State Council of China launched the Air Pollution Prevention and Control Action Plan in 2013 setting targets to reduce PM2.5 concentrations over the Beijing–Tianjin–Hebei region by 25 % from their 2013 levels by 2017 and to reduce annual mean PM2.5 concentrations in Beijing to 60 µg m−3 (Zheng et al., 2018; Wei et al., 2017). The mitigation strategies focused on long-term measures such as a gradual phase-out of residential biofuel use, changes in industrial technology, improved vehicle fuel standards, and the relocation of coal-fired power plants. The air quality in Beijing improved substantially during 2013–2017, and the annual mean PM2.5 concentration decreased from 89.5 µg m−3 in 2013 to 58 µg m−3 in 2017, largely due to the implementation of these long-term local and regional emission control measures (Ma et al., 2018; Cheng et al., 2019; Zheng et al., 2018).
While recent long-term emission reductions have brought substantial improvements in overall air quality, the region continues to experience frequent haze episodes characterized by high levels of PM2.5, particularly in winter (Dang and Liao, 2019; Xiao et al., 2020). Additional emergency measures generally lasting 3–7 d are necessary to prevent these extreme pollution episodes, especially under stable meteorological conditions that are conducive to the formation and accumulation of very high levels of particulate matter. Such short-term emission controls have been tested, with some success, during special events such as the 2008 Beijing Olympics, the Asia–Pacific Economic Cooperation (APEC) summit in 2014, and the China Victory Day Parade in 2015 (Zhang et al., 2015; Xu et al., 2019, 2017). However, the success of these controls has often been greatly aided by favourable weather conditions (Liu et al., 2017; Liang et al., 2017; Gao et al., 2017) and the same control strategies are liable to fail under different meteorological conditions. For example, while national air quality standards were met during the APEC summit, we have shown that they would have been greatly exceeded under the same emission controls had the summit been held 2 weeks earlier when the weather was less favourable (Ansari et al., 2019). Previous studies have advocated the application of emission controls over a wider geographical region (Guo et al., 2016; Wen et al., 2016; Ansari et al., 2019) but have not identified the spatial or temporal scales needed for successful policy implementation or proposed any general framework to devise future mitigation strategies that account for differing meteorological conditions. In this study we use a range of new modelling approaches, including 1 d emission reductions and statistical emulation, to gain a detailed understanding of the magnitude and timing of local and regional source contributions to PM2.5 concentrations in Beijing under varying meteorological conditions. We generate pollutant response surfaces based on these different emission sectors and regions and demonstrate how they can be used to guide the development of future short-term emission control policies in the city.
We use the Weather Research and Forecasting model with Chemistry (WRF-Chem) version 3.7.1 at a horizontal resolution of 27 km over China with nested domains over northern China at 9 km and the North China Plain at 3 km resolution. Gas-phase chemistry in the model is represented by the Carbon Bond mechanism version Z (CBMZ) which is coupled with the Model for Simulating Aerosol Interactions and Chemistry (MOSAIC) aerosol module with eight aerosol size bins (Zaveri and Peters, 1999; Zaveri et al., 2008). We use meteorological fields from the European Centre for Medium-Range Weather Forecasts (ECMWF) and anthropogenic emissions from residential, transport, industry, power generation, and agricultural sectors from the Multi-resolution Emission Inventory for China (MEIC) appropriate for 2014 (Li et al., 2017a). We take biomass burning emissions from the Fire Emissions INventory from NCAR (FINN; Wiedinmyer et al., 2011) and biogenic emissions from the Model of Emissions of Gases and Aerosols from Nature (MEGAN; Guenther et al., 2012). Further details of the model configuration and evaluation over North China are provided in a previous study where we explored emission controls in Beijing during the Asia–Pacific Economic Cooperation (APEC) summit in November 2014 (Ansari et al., 2019). In this previous study we demonstrated that the model can reproduce the magnitude of and variation in key pollutants over Beijing well and showed that meeting national air quality standards over the period was critically dependent on the weather conditions at the time. The formulation of effective short-term emission control policies therefore needs to account for the important role played by meteorological processes. In this study we focus on the same October–November period in 2014 and investigate the key source sectors and regions responsible for short-term pollution episodes during a range of meteorological conditions.
Figure 1 shows hourly observed and simulated PM2.5 concentrations for Beijing from 12 October to 19 November 2014. APEC emission controls were implemented from 3–12 November. The model has a positive mean bias of 22 µg m−3 over the October period, and we have previously demonstrated that this overestimation during episodes is principally due to insufficient boundary layer mixing (Ansari et al., 2019). In the last 15 d of October, only 3 of the days met the daily national Class 2 air quality standard of 24 h average PM2.5 concentration less than 75 µg m−3 (air quality index, AQI = 100), and 8 of the days exceeded the higher threshold for heavy pollution of 150 µg m−3 (AQI = 200). Reducing the 24 h average PM2.5 concentration below 75 µg m−3 over the entire period would require strict, carefully tailored emission reductions across multiple sectors and regions that are timed to provide maximum benefit during the heaviest pollution episodes.
For APEC, emission controls were implemented in two stages: an initial phase (APEC 1) that covered Beijing and some western districts of Hebei province including Baoding, Langfang, Shijiazhuang, Xingtai, and Handan and a second more stringent phase (APEC 2) that additionally covered Tianjin, Tangshan, Cangzhou, Hengshui, Dezhou, Binzhou, Dongying, Jinan, Liaocheng, and Zibo (Wen et al., 2016; Li et al., 2017b). In this study we consider three broad regions of control: local emissions from Beijing, near-neighbourhood emissions from the North China Plain, and far-neighbourhood emissions from surrounding provinces (see Fig. 2). The near-neighbourhood region used here is defined to match the APEC 2 control region described above. Since we have shown that the APEC controls applied over this period were insufficient to meet healthy air quality standards (Ansari et al., 2019), we consider a far-neighbourhood region which covers parts of Shanxi, Shaanxi, Shandong, Henan, Inner Mongolia, Liaoning, and Jilin provinces. This covers most of our second model domain, as shown in Fig. 2; the outer model domain (not shown) covers the whole of China.
A number of measurement and modelling studies have investigated source apportionment of air pollution in Beijing. Most measurement studies have used the positive matrix factorization (PMF) technique which effectively attributes PM2.5 to different emission sectors but does not provide the district-based regional contributions critical for policymaking (Zhang et al., 2013; Zíková et al., 2016; Shang et al., 2018). Li et al. (2014) developed a tagging approach using the Nested Air Quality Prediction Modelling System (NAQPMS), which apportions primary aerosols to their emission sources and secondary aerosols to their geographic region of formation. However, from the perspective of control policy formulation for secondary-aerosol-dominated episodes, it would be more valuable to apportion secondary aerosols to specific precursor emission sources rather than their region of formation. Li et al. (2015) performed a comprehensive modelling study using the Particulate Matter Source Apportionment Technology (PSAT) emissions-tagging approach in the Comprehensive Air Quality Model with Extensions (CAMx) at a relatively coarse resolution of 36 km to derive district-based source contributions. However, this approach does not capture the interactions between secondary PM precursor species which may be particularly important during episodes with high nitrate levels (Burr and Zhang, 2011). Recently, Chen et al. (2019) used the PSAT approach at 12 km resolution to calculate source contributions from districts included in the Chinese government's “2+26” regional emission control strategy, although they did not include the effect of surrounding regions in their analysis, which may be needed to formulate successful emission control policy under less favourable meteorological conditions. Moreover, none of these studies provide information on the temporal contribution of different sources, which is important for the design of short-term emergency control measures. Matsui et al. (2009) performed a simple exploration of the temporal nature of source contributions from different regions. They found that primary aerosols in Beijing are affected by emissions within 100 km in the previous 24 h and secondary aerosols over Beijing are affected by emission sources within 500 km in the previous 3 d. However, a more detailed understanding of the temporal nature of regionally resolved sectoral source contributions under a range of meteorological conditions is required to aid robust short-term emission control policymaking for Beijing.
With the aim of informing short-term emission reduction policies, we investigate the temporal contributions from different emission sectors and regions by conducting a number of different simulation experiments. In Sect. 3 we determine the contribution from each day of anthropogenic emissions over each major emission region to the temporal evolution of pollutant levels in Beijing. We investigate the total contribution from each sector and region in Sect. 4. In Sect. 5 we then explore the sensitivity of pollutant levels in Beijing to all sectors and regions simultaneously using Gaussian process emulation and build pollutant response surfaces for Beijing that can be used to determine the emission reductions needed to meet specified air quality standards.
To ensure good air quality, regional short-term emission controls have been implemented for high-profile events in Beijing over the past decade, including the 2008 Olympics, the 2014 APEC meeting, and the 2015 China Victory Day parade. These controls resulted in improved air quality, although for all three events the successful outcomes were greatly aided by favourable meteorological conditions (Yang et al., 2011; Liang et al., 2017). In each case, emission controls were initiated substantially before the event: 18 d before for the Olympic games in 2008 (Gao et al., 2011; Yang et al., 2011), 7 d before for the APEC meeting in 2014 (Zhang et al., 2016; Sun et al., 2016), and 14 d before for the Victory Parade in 2015 (Liang et al., 2017; Zhao et al., 2017b). This period allowed emission controls to take effect and existing pollution to be swept away, but the optimal timing for controls that balances improvements in air quality against the economic and social costs of implementing them remains unclear. To resolve this, it is important to understand how pollution from previous days and different regions builds up under different meteorological conditions and to determine the persistence of pollution from a single day of emissions.
We consider three regions of control: Beijing, near-neighbourhood, and far-neighbourhood (see Fig. 2); we conduct 60 5 d long model runs, 20 for each region, with emission reductions for the first day of the simulation only and standard baseline emissions for subsequent days (see Fig. S1). Each of these runs was initialized directly from the baseline simulation without the need for an additional spin-up period. We apply emission reductions following those implemented during the APEC summit period: 40 %–50 % for Beijing and 30 %–35 % for surrounding districts (see Ansari et al., 2019). The period of interest was selected to cover a range of different meteorological conditions and includes a polluted period in mid to late October (14 d) and a cleaner period in early to mid November (also 14 d in length). The difference in simulated PM2.5 concentrations between each model run and the baseline run gives the contribution from the sources on a specific day over subsequent days.
Figure 3 shows the contribution of 1 d emission changes applied across all three regions to PM2.5 in Beijing for 21–27 October 2014. While emission reductions on a given day make a substantial contribution to PM2.5 on that day, the benefits often extend to a number of subsequent days due to the meteorological conditions and timescales for transport. The most polluted days (e.g. 24 and 25 October) show accumulated contributions to PM2.5 from as much as 5 d previously. Under clean, northwesterly winds, the pollution is swept away over the North China Plain, and the resulting clean days are dominated by fresh pollution from the same day, as seen on 26 October. The daily contributions vary substantially in magnitude as well as in timing, and pollution levels are typically higher at nighttime when the planetary boundary layer (PBL) is shallower, allowing local pollutants to build up.
To gain insight into how meteorological processes affect the timescales for transport from different regions, we explore the contributions from the Beijing, near-neighbourhood, and far-neighbourhood regions separately. Figure 4 presents the contributions to PM2.5 concentrations in Beijing from 1 d emission reductions relative to the day of control for the three different source regions over the 28 d period considered here. Contributions from Beijing sources affect PM2.5 in Beijing immediately and typically last 1–2 d, with peak contributions ranging from 8–43 µg m−3 (median value 21 µg m−3) and occurring towards the end of the day of emissions control. Contributions from the near-neighbourhood region are somewhat delayed and typically extend until the third day. The contributions are generally smaller than those from Beijing sources and are greatest on the second day. Contributions from the far-neighbourhood region are more spread out and are further delayed in time, with very little contribution over Beijing on the day of control. The contributions are greatest in the 2 d following controls, reflecting the timescales for transport, and can persist for as much as 5 d. Figure 4b, d, and f show 24 h average contributions from each of the three source regions and highlight the variability in the magnitude and duration of the influence from a given day of emissions that is driven by the prevailing meteorological conditions.
The highest hourly contribution from local controls in Beijing (43 µg m−3) occurs for emissions on 25 October, which is one of the most polluted days during the study period (see Fig. 1). The highest hourly contribution from near-neighbourhood controls is similar in magnitude (also 43 µg m−3) and occurs from emissions on 23 October which are trapped over Beijing during the pollution episode of 24 and 25 October. Similarly, the highest contribution from far-neighbourhood pulses occurs during the same pollution episode and arises from emissions 1 d earlier, on 22 October.
To characterize the source contributions for each simulation, we calculate the magnitude and timing of the peak contribution, the integrated contribution, and its duration (see Table S1 in Supplement). During the polluted period in October, the highest integrated contribution comes from Beijing sources on 5 of the 10 d, from near-neighbourhood sources on 4 d, and from far-neighbourhood sources on 1 d. During the cleaner period in November, the highest integrated contribution is from Beijing sources on almost all occasions (9 out of 10 d), and far-neighbourhood sources make a greater contribution than near-neighbourhood sources on 8 of the days. Local Beijing sources are responsible for the highest peak contributions on 6 of the days in October and for all 10 d in November. However near-neighbourhood sources also make a major contribution on polluted days. Far-neighbourhood sources showed higher contributions than near-neighbourhood sources for 7 of the days in November, but these were substantially smaller than contributions from Beijing sources. The effect of Beijing sources rarely extends to the end of the second day, whereas the contributions from more distant sources can extend to almost 5 d. The greatest contributions from all regions occur in late afternoon or early evening in Beijing, reflecting the accumulation of pollutants in the more stable evening boundary layer, along with accumulation from rush hour traffic sources.
While the temporal contributions from each region show distinct mean behaviour, they also show significant variability associated with the differing meteorological conditions each day. To examine the effect of meteorology, we investigate the relationship between peak and integrated contributions and meteorological parameters such as daily average wind speed and direction. Some key relationships are shown in Fig. 5. We find that peak contributions from Beijing sources show a clear negative correlation (r value of −0.74) with average wind speed in Beijing on the day of the emissions. This is as expected and reflects the greater build up of pollutants under more stagnant conditions. The wind speed on subsequent days does not show a clear relationship with the contributions from any of the sources. The integrated contribution from all three source regions is higher when the wind is blowing from the south. This reflects the fact that the strongest regional emission sources lie over the North China Plain south of Beijing. Higher integrated contributions were seen during southerly winds when the wind speed was lower, demonstrating the importance of the build up of pollutants from across the North China Plain under more stable, anticyclonic conditions. Winds from other sectors were generally stronger and led to very little contribution from regional sources over Beijing.
Overall, it is clear that local emission controls in Beijing provide an immediate but typically relatively short-lived benefit to air quality in the city, with the magnitude of the benefit dependent on whether stagnant meteorological conditions with low wind speed are prevailing. Regional emission controls over the North China Plain generally lead to smaller benefits which start later and last longer, although their contribution may rival those from local emissions under weak, southerly winds. More distant regions may also make a contribution under these conditions, although these typically take a number of days to build up. These results suggest that mitigating major pollution episodes in Beijing requires control of local emissions 1 or 2 d in advance, control of near-neighbourhood emissions 2 to 3 d in advance, and control of far-neighbourhood emissions 3 to 4 d in advance.
An understanding of the contribution from individual sectors (industry, transport, residential, and power generation) from different regions is also important to inform successful emission control policies. To determine the impact of each source sector in each different region, we conduct model simulations where each of the 12 emission sources (four sectors over three regions) was removed in turn for the period of 21–31 October. We conducted an additional run with all 12 emission sources removed to provide an estimate of background contributions from sources outside the regions and from biogenic, agricultural, and biomass burning sources inside the regions. Each sensitivity run was initialized from baseline concentration fields at midnight UTC on 20 October, and the emission changes were implemented at 16:00 h UTC to reflect emission controls from midnight local time.
The October simulation period is characterized by two distinct pollution episodes: 21–25 October (episode 1) and 26–30 October (episode 2). During each episode the total PM2.5 concentration over Beijing builds up over a 5 d period and peaks on the fifth day. Figure 6 shows hourly time series of contributions from each emission source. In general, residential and industrial sectors make much greater contributions than the power and transport sectors. The contribution of Beijing emission sources shows a more pronounced diurnal variation than that of the regional sources. This is because the Beijing plume is still fresh and contains the diurnal signal of local emissions, whereas regional plumes are transported to Beijing over longer distances and are better mixed, losing this diurnal signal. All sources show a build-up during the two episodes, but the rate of this increase is high for Beijing sources, low for near-neighbourhood sources and lower still for far-neighbourhood sources. Far-neighbourhood contributions show a delayed onset for this increase compared with those from nearer sources, highlighting that 3–4 d of stagnation over Beijing are needed before far-neighbourhood sources start to make a substantial contribution. This is consistent with our findings on the temporal response to emission changes in Sect. 3. It is interesting to note that the source contributions do not peak at the same time, and therefore the maximum concentrations of PM2.5 do not reflect the maximum contributions from each source. Figure 6 reveals the anatomy of the two PM2.5 episodes shown in Fig 1 and shows that episode 1 was dominated by regional pollution, particularly industrial, residential, and transport emissions from near-neighbourhood sources, while episode 2 had greater influence from local residential emissions, which exceeded the contributions from regional emissions. This is because episode 1 experienced stronger southwesterly winds during 23–24 October (4 m s−1) that brought PM2.5 from high-emission sources south of Beijing enabling greater accumulation over the city before it was swept away by the clean northeasterly winds the next day. Episode 2 experienced weak southeasterly winds during 29–30 October (2 m s−1), which did not bring as much PM2.5 from neighbouring sources but allowed local emissions to build up under calmer conditions. See Fig. S2 in the Supplement for more details of the meteorological conditions during this period.
Figure 7 presents absolute and relative contributions to daily mean PM2.5 in Beijing from the 12 emission sources along with those from background sources. The remaining difference between the sum of these contributions and the baseline PM2.5 concentrations is attributed to interactions between emissions from different sources. The largest contributions are from Beijing and near-neighbourhood sources on most days, which average 35 % and 32 % respectively. However, far-neighbourhood sources make a substantial contribution (up to 28 %) on polluted days. The two episodes have different characteristics, as noted above, with the first episode more greatly affected by near-neighbourhood emissions, while the second showed a greater influence from local emissions, notably from the residential sector. The spatial distribution of 24 h average PM2.5 for the 2 d is shown in Fig. 8, which reveals the differing extents of the episodes. Elevated PM2.5 concentrations were present over a much wider area during the first episode, and the contributions from near-neighbourhood sources were substantially higher. The differences between these two pollution episodes just 5 d apart emphasizes the importance of meteorological processes in governing the contributions of different sources. Note that the baseline concentration fields shown in the leftmost panels also include contributions from background and natural sources as well as from local, near-neighbourhood, and far-neighbourhood emissions before the start of simulations.
The contributions of key sources build up consistently over the course of each pollution episode. A sizable portion of PM2.5 is attributed to interactions between gas-phase precursors from different sources and this reflects non-linear processes, particularly the formation of secondary aerosols (Zhao et al., 2017a). In general, days with higher contributions from transport and power sectors show the greatest interactions. These sectors are major sources of nitrogen dioxide (NO2) and sulfur dioxide (SO2) respectively, and this non-linear behaviour can be explained by competition between SO2 and NO2 in the presence of ammonia (NH3) to form sulfate and nitrate aerosols. A reduction in power sector emissions alone reduces SO2 and therefore ammonium sulfate particles ((NH4)2SO4), thereby freeing up NH3 gas which may then react with NO2 to form ammonium nitrate particles (NH4NO3). This leads to little change in total PM2.5 concentrations, offsetting the benefits of the emission reduction. Reducing emissions from both power and transportation sectors reduces the NO2 available to react with the freed NH3, leading to more efficient PM2.5 reduction.
To place the sectoral and temporal attribution approaches used here into context, we compare the cumulative contributions from 1 d emission controls across all sectors with those from continuous emission controls on individual sectors. We scale the contributions from individual sectors by 45 % for Beijing sources and by 35 % for regional sources to match the APEC-like emission reductions applied in the 1 d control runs described in Sect. 3. A comparison of the cumulative contributions to PM2.5 in Beijing from successive 1 d pulses and from different emission sectors is shown for each source region in Fig. 9. Local sources predominantly affect PM2.5 on the day of emission, although they may have a substantial effect on the second day under polluted conditions, as is evident from emissions on 24 October. Sources over neighbouring provinces have a more prolonged effect, and there may be substantial contributions from as many as 4 d previously during polluted episodes such as on the evening of 25 October. On clean days, such as 26 October, the contribution of these sources is negligible. A sectoral analysis shows that residential and industrial sectors make the biggest contribution to PM2.5 in Beijing from local sources, with the former typically dominating during the evenings when pollutant levels peak. PM2.5 from neighbouring provinces is dominated by industrial sources, and while residential sources are also important, there is also a significant contribution from transportation sources during the pollution episode when air arrives in Beijing from the North China Plain. The cumulative contributions of different sources based on 1 d emission controls are very similar to those from the continuous sectoral controls (see Fig. S3), demonstrating that the two approaches give comparable responses. This lends confidence in our independent attribution of the temporal and sectoral contributions to PM2.5 in Beijing and suggests that secondary particle production associated with interactions between precursors from different sectors and regions plays a relatively small role.
Assessing the combined effect of different emission changes and the non-linear response of secondary aerosol to precursor emissions from different sources requires that emission changes are applied across a number of sources at the same time. However, exploring all combinations of emission regions and sectors considered here would be computationally prohibitive. We therefore apply a computationally fast surrogate model to fully explore these relationships in a computationally tractable manner. We choose a Gaussian process-based statistical emulator as a surrogate model as it requires relatively few training runs and is well-suited to mapping the non-linear but continuous relationship between emissions and concentrations characteristic of PM2.5 (see Ryan et al., 2018; Chen et al., 2020). We focus here on 12 emission sources that include the four key sectors in each of the three regions considered here. To define the model training runs, we use maximin Latin hypercube sampling, following Lee et al. (2011), to select 60 distinct sets of emission changes in the range 0 %–120 % to apply to the 12 sources considered here (see Table S2 in the Supplement for the values used). We perform WRF-Chem model simulations for each of these 60 emission scenarios, initialized from the baseline simulation, for the period 21–31 October and build emulators for daily PM2.5 in Beijing for each day of the period (11 emulators in total) using the model output. The emulators are built using the DICE-Kriging package in R (Roustant et al., 2012), following the approach of Ryan et al. (2018). We validate the emulators using a leave-one-out approach, successively rebuilding all 11 emulators using only 59 of the 60 model outputs and comparing them against the remaining one. The agreement between the model and emulator outputs results in an R2 of 0.99 (see Fig. S4) indicating that the emulators reproduce the model PM2.5 concentrations very well.
We first demonstrate the use of the emulators to investigate the contribution of each emission source to PM2.5 in Beijing by performing global sensitivity analysis. This provides a robust method for identifying which sources most affect simulated PM2.5 concentrations. We calculate a global sensitivity index for each source which quantifies its contribution to the total variance in PM2.5 across all combinations of changes in other sources (Lee et al., 2013; Ryan et al., 2018). We use the computationally efficient extended Fourier Amplitude Sensitivity Test (eFAST) algorithm (Saltelli et al., 1999) to compute these global sensitivity indices. The eFAST algorithm needs thousands of model evaluations from across the emission parameter space considered, and while this would be computationally prohibitive with the WRF-Chem model, it is relatively straightforward with the emulators. We conduct 10 000 runs with the emulators to calculate global sensitivity indices for each of the 12 emission sources. Since these sensitivity indices are based on the variance in PM2.5, we take the square root to permit a direct comparison with the contributions calculated using one-at-a-time local sensitivity analysis as described in Sect. 4. We find that the relative contributions from the different regions and sectors derived through these different approaches are generally very similar; see Fig. S5. However, we note that power and transport sectors, which are the dominant sources of precursor gases for secondary inorganic aerosol formation, show slightly higher contributions calculated this way than when derived from one-at-a-time source changes, reflecting the importance of interactions between these sectors for secondary aerosol formation. These results lend confidence in the use of the emulators and demonstrate the additional value that they provide.
Concentration response surfaces were developed for daily average PM2.5 in Beijing for each day of the period (21–31 October) using the emulators. Figure 10 presents response surfaces for some key combinations of emission sources for 24 October, the day with highest PM2.5 concentrations. PM2.5 responses to changes in key sectors across all source regions together are shown in Fig. 10a–c. Emission reductions in the transport sector are more efficient than those in the power sector in reducing total PM2.5 over Beijing (Fig. 10a); an 80 % reduction in transport emissions results in a reduction of 30 µg m−3 (from 343 to 313 µg m−3), while the same reduction in the power sector leads to a reduction of only 16 µg m−3. Non-linearity in the PM2.5 response is also evident here; for example, a reduction in the transport sector by 60 % with no change in the power sector leads to a reduction in PM2.5 of 20 µg m−3 (343 to 323 µg m−3), whereas the same reduction applied when the power sector is at 20 % strength reduces PM2.5 by 27 µg m−3 (327 to 300 µg m−3). These response surfaces demonstrate that the industrial sector makes the greatest contribution to PM2.5 in Beijing, closely followed by the residential sector, and that strong controls on these two sectors alone would bring PM2.5 concentrations down towards 150 µg m−3 under the conditions prevailing on this day.
Response surfaces for emission changes over different source regions with all sectors combined are shown in Fig. 10d–e. Near-neighbourhood sources make the greatest contributions to PM2.5 in Beijing under these polluted conditions, with smaller contributions from Beijing and far-neighbourhood sources. An 80 % reduction in near-neighbourhood sources alone would reduce PM2.5 concentrations by 121 µg m−3, and the dominant emissions sector in this region, industrial sources, is responsible for 53 µg m−3 of this (Fig. 10f). However, it is clear that reductions in specific regions or sectors alone are insufficient to bring PM2.5 concentrations below 150 µg m−3. We therefore show the effect of combined emission reductions in Fig. 10g–i. Reduction in emissions of 80 % across all 12 sources bring PM2.5 levels down to 130 µg m−3, a drop of 213 µg m−3. This remains insufficient to meet the national air quality standard of daily average PM2.5 concentrations below 75 µg m−3. Meeting this standard would require the removal of all emission sources from these sectors for all three regions, which would bring down the levels to 79 µg m−3. Greater reductions in PM2.5 concentrations on 24 October would require emission controls to be applied 1 or 2 d earlier than the start of the period considered here, 21 October, as demonstrated in Sect. 3. Nonetheless, we demonstrate that these response surfaces provide valuable guidance on the reductions in PM2.5 in Beijing that are possible from different combinations of emission reductions without the need to perform additional air quality model simulations.
The response surfaces can be used to explore the effects of a wide range of possible emission control scenarios. We show examples of these for daily mean PM2.5 in Beijing in Fig. 11. For the emission reductions applied during the APEC period, we find reductions in PM2.5 of about 23 %, very similar to those derived from an independent model simulation using these emission changes (Ansari et al., 2019). Extending the same emission controls to a wider region over far-neighbourhood provinces would lead to an additional improvement, giving a total reduction in PM2.5 of 27 %, but this remains insufficient to meet even the secondary air quality standard of 150 µg m−3 on 24 October. Meeting this standard would require an emission reduction of 90 % across all Beijing and near-neighbourhood sources. Alternatively, it could be met with an emission reduction of 80 % across all Beijing and near-neighbourhood sources along with a reduction of 40 % across all far-neighbourhood sources. The choice of source reductions needed to meet a given standard can be taken directly from the corresponding response surface (see Fig. 10). Meeting the primary air quality standard of 75 µg m−3 on 30 October would be possible with a reduction of 85 % across Beijing and near-neighbourhood sources and 80 % across far-neighbourhood sources; see Fig. 11. The standard would still be exceeded on 24 and 25 October under these conditions, but we note that our period of interest started on 21 October, only 3 d before this pollution episode. As shown earlier, emissions over more distant regions from 4–5 d previously affect Beijing during this pollution episode, and controls would have been needed before 21 October, perhaps over an even wider region than we consider here, to meet the standards over this full period.
We note that there have been considerable reductions in emissions since 2014 as a result of the Chinese government's clean-air policies, which have included ultra-low emission standards for power plants, the phase-out of outdated industrial infrastructure, the replacement of coal with natural gas for residential heating, and higher fuel standards for vehicles. These have led to a significant improvement in air quality (Zhang et al., 2019; Zheng et al., 2018). Between 2014 and 2017, observed annual average PM2.5 concentrations dropped from 100 to 64 µg m−3 in the Beijing–Tianjin–Hebei region (Wang et al., 2020) and from 86 to 58 µg m−3 in Beijing (Cheng et al., 2019).
To explore the effect of recent emission changes, we apply emission reductions for Beijing (75 % for industry and power sources, 80 % for residential sources, and no change for traffic sources) and for neighbouring provinces (40 % for industry and power, 30 % for residential sources, no change for traffic sources) that reflect recent emission assessments (Cheng et al., 2019; Zheng et al., 2018). We find that daily mean PM2.5 concentrations in Beijing over the October period examined here are reduced by an average of 36 %, close to the observed annual reduction of 33 %. However, PM2.5 concentrations still peak at 253 and 175 µg m−3 during the episodes of 24 and 30 October respectively, and these levels remain well above the national daily air quality standard. Recent independent modelling studies have highlighted the continued persistence of haze episodes in the region even after the implementation of clean-air policies (Dang and Liao, 2019; Li et al., 2019). This emphasizes that short-term emergency measures remain indispensable for avoiding the most severe haze episodes, and our study provides a guiding framework for their formulation.
We carefully chose a period covering a diverse set of meteorological conditions for our temporal, sectoral, and global sensitivity analyses (see Table S2 and Fig. S2 in Ansari et al., 2019, for more details on meteorological conditions during the study period); however, our approaches are fully generalizable and can be applied to other longer periods and different seasons in order to build an even more general picture.
In this study we have investigated the temporal, regional, and sectoral contributions to particulate air pollution in Beijing in autumn using a high-resolution regional air quality model with the aim of informing short-term emission control policies to mitigate major PM2.5 pollution episodes. We find that the effects of local emission reductions in Beijing can be substantial but typically only contribute about 20 % of PM2.5 concentrations during pollution episodes, and the effects rarely extend beyond the day of emissions reduction. Controls on emissions in neighbouring regions over the North China Plain have a larger impact on PM2.5 in Beijing, typically about 35 % during pollution episodes, peaking the day following the application of controls, and they can persist for a number of days. Emissions from more distant regions over North China can also have a substantial impact under some meteorological conditions, and the effect of emission changes are more dispersed and may persist over Beijing for as much as 5 d. Using simple one-at-a-time sensitivity studies, we identify industrial and residential emissions from near-neighbourhood regions of the North China Plain as the two largest sources of PM2.5 in Beijing, although there is substantial variability in their contributions driven by meteorology, and on cleaner days under northwesterly flow PM2.5 concentrations are principally from local Beijing sources, particularly from the residential and industrial sectors.
To provide a more comprehensive analysis of source contributions that accounts for the interactions between precursors from different sectors and regions, we apply Gaussian process emulation to derive response surfaces for daily PM2.5 concentrations in Beijing and demonstrate how these may be used to guide the choice of emission controls to meet specific air quality standards. Focusing on a polluted period in October 2014, we show that large emission reductions exceeding 80 % may be needed to meet standards but that the magnitude of the reductions depends on the regional extent of the controls and on their timing. Controls focused on the North China Plain alone may be insufficient to keep air quality within the national standards, and this provides strong support for the application of controls over a wider area such as those implemented in the recent “2+26” programme (Chen et al., 2019). While we have focused on the October–November 2014 period associated with the important APEC Summit to explore source sensitivities, we note that emissions are changing rapidly in both Beijing and surrounding regions (Cheng et al., 2019; Zheng et al., 2018) leading to spatial and temporal changes in air pollution (Xiao et al., 2020; Xu and Zhang, 2020). The temporal sensitivity and emulation approaches we have demonstrated here may nonetheless serve as a valuable guide in policy formulation for Beijing during the autumn and winter period. More generally, these methods could be used to build a formal framework to guide policy decisions aimed at mitigating short-term air pollution episodes throughout the year and may be equally valuable in other cities around the world.
The WRF-Chem model code is available from http://www2.mmm.ucar.edu/wrf/users/download/ (Skamarock et al., 2008). The model configuration and surface pollutant distributions generated in this study are available from the Lancaster University data archive at https://doi.org/10.17635/lancaster/researchdata/423 (Ansari and Wild, 2021) and https://doi.org/10.17635/lancaster/researchdata/300 (Ansari, 2019).
The supplement related to this article is available online at: https://doi.org/10.5194/acp-21-4471-2021-supplement.
TUA, OW, and ZW designed this study, and TUA performed the model simulations, analysis, and visualization. JL provided emissions data and expertise on the model configuration. ER generated code for emulating the model output. YC provided scientific expertise and critical support on model operation. TUA and OW prepared the paper with input from all co-authors.
The authors declare that they have no conflict of interest.
Tabish Umar Ansari and Oliver Wild thank the UK Natural Environment Research Council for support. Jie Li thanks the National Natural Science Foundation of China. Tabish Umar Ansari acknowledges Dennis Shea, Adam Philips, Rashed Mahmood, and Rick Brownrigg of the “ncl-talk” online forum for providing assistance on data visualization and thanks the Lancaster Environment Centre for providing funding to carry out his PhD research.
This research has been supported by the UK Natural Environment Research Council (grant nos. NE/N006925/1 and NE/N006976/1) and by National Natural Science Foundation of China (grant nos. 41571130034 and 91744203).
This paper was edited by Pedro Jimenez-Guerrero and reviewed by two anonymous referees.
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