Abstract

Abstract. Tropospheric ozone is important to future air quality and climate. We investigate ozone changes and ozone sensitivity to changing emissions in the context of climate change from the present day (2004–2014) to the future (2045–2055) under a range of shared socio-economic pathways (SSPs). We apply the United Kingdom Earth System Model, UKESM1, with an extended chemistry scheme including more reactive volatile organic compounds (VOCs) to quantify ozone burdens as well as ozone sensitivities globally and regionally based on nitrogen oxide (NOx) and VOC mixing ratios. We show that the tropospheric ozone burden increases by 4 % under a development pathway with higher NOx and VOC emissions (SSP3-7.0) but decreases by 7 % under the same pathway if NOx and VOC emissions are reduced (SSP3-7.0-lowNTCF) and by 5 % if atmospheric methane (CH4) mixing ratios are reduced (SSP3-7.0-lowCH4). Global mean surface ozone mixing ratios are reduced by 3–5 ppb under SSP3-7.0-lowNTCF and by 2–3 ppb under SSP3-7.0-lowCH4. However, surface ozone changes vary substantially by season in high-emission regions under future pathways, with decreased ozone mixing ratios in summer and increased ozone mixing ratios in winter when NOx emissions are reduced. VOC-limited areas are more extensive in winter (7 %) than in summer (3 %) across the globe. North America, Europe, and East Asia are the dominant VOC-limited regions in the present day, but North America and Europe become more NOx-limited in the future mainly due to reductions in NOx emissions. The impacts of VOC emissions on ozone sensitivity are limited in North America and Europe because reduced anthropogenic VOC emissions are partly offset by higher biogenic VOC emissions. Ozone sensitivity is not greatly influenced by changing CH4 mixing ratios. South Asia becomes the dominant VOC-limited region under future pathways. We highlight that reductions in NOx emissions are required to transform ozone production from VOC to NOx limitation, but that these lead to increased ozone mixing ratios in high-emission regions, and hence emission controls on VOC and CH4 are also necessary.

Highlights

  • Ozone (O3) is a chemically reactive component in the atmosphere that is produced from natural and anthropogenic sources

  • The interactions between air quality and climate play an important role in the coupled Earth system, and we focus on the impacts of future emissions in the context of climate change on tropospheric O3 in this study

  • Insufficient turbulent mixing in the planetary boundary layer may contribute to the bias (O’Connor et al, 2014), as accumulation of nitrogen oxides (NOx) at the surface leads to greater O3 production in summer and greater titration by nitric oxide (NO) in winter

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Summary

Introduction

Ozone (O3) is a chemically reactive component in the atmosphere that is produced from natural and anthropogenic sources. O3 sensitivity is typically characterised by NOx- or VOClimited regimes for O3 production, and this determines the effectiveness of different emission control strategies. It is dependent on the relative abundances of NOx and VOC (Sillman, 1999) or of their oxidation products, nitric acid (HNO3). We quantify O3 sensitivity based on the ratio of NOx and VOC mixing ratios and investigate how regional O3 sensitivity might change in the future. We compare and evaluate the present-day tropospheric O3 burden and surface O3 mixing ratios with two different chemistry schemes in Sect. 4. Analysis of O3 mixing ratios and production is used to quantify O3 sensitivity and to explain contrasting regional O3 changes in Sect.

Materials and methods
Emissions and experiments
O3 sensitivity indicators
Comparison of StratTrop and extended chemistry schemes
Evaluation of surface O3 mixing ratios
Emission changes
Tropospheric O3 changes
Surface seasonal O3 changes
O3 sensitivity in the present day and the future
Spatial distributions of O3 sensitivity
Conclusions
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