Abstract

Abstract. We examine the street-scale variation of NOx, NO2, O3 and PM2.5 concentrations in Beijing during the Atmospheric Pollution and Human Health in a Chinese Megacity (APHH-China) winter measurement campaign in November–December 2016. Simulations are performed using the urban air pollution dispersion and chemistry model ADMS-Urban and an explicit network of road source emissions. Two versions of the gridded Multi-resolution Emission Inventory for China (MEIC v1.3) are used: the standard MEIC v1.3 emissions and an optimised version, both at 3 km resolution. We construct a new traffic emissions inventory by apportioning the transport sector onto a detailed spatial road map. Agreement between mean simulated and measured pollutant concentrations from Beijing's air quality monitoring network and the Institute of Atmospheric Physics (IAP) field site is improved when using the optimised emissions inventory. The inclusion of fast NOx–O3 chemistry and explicit traffic emissions enables the sharp concentration gradients adjacent to major roads to be resolved with the model. However, NO2 concentrations are overestimated close to roads, likely due to the assumption of uniform traffic activity across the study domain. Differences between measured and simulated diurnal NO2 cycles suggest that an additional evening NOx emission source, likely related to heavy-duty diesel trucks, is not fully accounted for in the emissions inventory. Overestimates in simulated early evening NO2 are reduced by delaying the formation of stable boundary layer conditions in the model to replicate Beijing's urban heat island. The simulated campaign period mean PM2.5 concentration range across the monitoring network (∼15 µg m−3) is much lower than the measured range (∼40 µg m−3). This is likely a consequence of insufficient PM2.5 emissions and spatial variability, neglect of explicit point sources, and assumption of a homogeneous background PM2.5 level. Sensitivity studies highlight that the use of explicit road source emissions, modified diurnal emission profiles, and inclusion of urban heat island effects permit closer agreement between simulated and measured NO2 concentrations. This work lays the foundations for future studies of human exposure to ambient air pollution across complex urban areas, with the APHH-China campaign measurements providing a valuable means of evaluating the impact of key processes on street-scale air quality.

Highlights

  • In recent decades, China’s rapid economic growth, industrialisation and urbanisation have led to severely deteriorating air quality

  • Sensitivity studies explore the impact on model performance of including explicit road emission sources, varying diurnal emissions profiles and accounting for the evening urban heat island (UHI) in Sects. 3.5, 3.6 and 3.7, respectively

  • Measurements recorded at 12 of Beijing’s air quality monitoring network stations and at the Institute of Atmospheric Physics (IAP) field site are compared with simulated pollutant levels generated by the Multi-resolution Emission Inventory for China v1.3 (MEIC Std), at 3 km resolution, and an optimised version of the same inventory (MEIC Opt)

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Summary

Introduction

China’s rapid economic growth, industrialisation and urbanisation have led to severely deteriorating air quality. Measured concentrations at 12 national air quality monitoring stations, run by the China National Environmental Monitoring Center (CNEMC), the IAP field site and an additional site 60 km south-east of Beijing, situated in the built-up Guangyang district of Langfang in Hebei province, are used to estimate this background concentration field. To approximate background values for gaseous species (NO2, O3, CO and SO2), the hourly minimum concentration for each pollutant across the 12 network monitoring stations and the IAP field site is selected, yielding an approximation for the underlying conditions uninfluenced by local sources

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