Abstract

Abstract. Ozone (O3) from 17 atmospheric chemistry models taking part in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP) has been used to calculate tropospheric ozone radiative forcings (RFs). All models applied a common set of anthropogenic emissions, which are better constrained for the present-day than the past. Future anthropogenic emissions follow the four Representative Concentration Pathway (RCP) scenarios, which define a relatively narrow range of possible air pollution emissions. We calculate a value for the pre-industrial (1750) to present-day (2010) tropospheric ozone RF of 410 mW m−2. The model range of pre-industrial to present-day changes in O3 produces a spread (±1 standard deviation) in RFs of ±17%. Three different radiation schemes were used – we find differences in RFs between schemes (for the same ozone fields) of ±10%. Applying two different tropopause definitions gives differences in RFs of ±3%. Given additional (unquantified) uncertainties associated with emissions, climate-chemistry interactions and land-use change, we estimate an overall uncertainty of ±30% for the tropospheric ozone RF. Experiments carried out by a subset of six models attribute tropospheric ozone RF to increased emissions of methane (44±12%), nitrogen oxides (31 ± 9%), carbon monoxide (15 ± 3%) and non-methane volatile organic compounds (9 ± 2%); earlier studies attributed more of the tropospheric ozone RF to methane and less to nitrogen oxides. Normalising RFs to changes in tropospheric column ozone, we find a global mean normalised RF of 42 mW m−2 DU−1, a value similar to previous work. Using normalised RFs and future tropospheric column ozone projections we calculate future tropospheric ozone RFs (mW m−2; relative to 1750) for the four future scenarios (RCP2.6, RCP4.5, RCP6.0 and RCP8.5) of 350, 420, 370 and 460 (in 2030), and 200, 300, 280 and 600 (in 2100). Models show some coherent responses of ozone to climate change: decreases in the tropical lower troposphere, associated with increases in water vapour; and increases in the sub-tropical to mid-latitude upper troposphere, associated with increases in lightning and stratosphere-to-troposphere transport. Climate change has relatively small impacts on global mean tropospheric ozone RF.

Highlights

  • Ozone (O3) is a radiatively active gas in Earth’s atmosphere, interacting with down-welling and up-welling solar and terrestrial radiation

  • This paper looks in detail at tropospheric ozone radiative forcings (RFs) from the ACCMIP simulations

  • Net ozone RFs larger by 5–41 mW m−2 (1–10 %), with MASK150 compared to MASKZMT (Table 3; the ranges quoted cover the full model spread)

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Summary

Introduction

Ozone (O3) is a radiatively active gas in Earth’s atmosphere, interacting with down-welling and up-welling solar (shortwave, SW) and terrestrial (longwave, LW) radiation. Any changes in the atmospheric distribution of ozone contribute to the radiative forcing of climate change (e.g., Lacis et al, 1990; Forster et al, 2007). The focus of this paper is the troposphere, where ozone is thought to have substantially increased since the pre-industrial era, exerting a warming influence on surface climate. Tropospheric ozone is a secondary pollutant produced during the photochemical oxidation of methane (CH4), carbon monoxide (CO) and non-methane volatile organic compounds (NMVOC) in the presence of nitrogen oxides (NOx) (Crutzen, 1974; Derwent et al, 1996). Completing its budget, ozone is removed from the troposphere by several chemical reactions (Crutzen, 1974), and is dry deposited at the surface, mainly to vegetation (Fowler et al, 2009)

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