Abstract

Abstract. Because tropospheric ozone is both a greenhouse gas and harmful air pollutant, it is important to understand how anthropogenic activities may influence its abundance and distribution through the 21st century. Here, we present model simulations performed with the chemistry–climate model SOCOL, in which spatially disaggregated chemistry and transport tracers have been implemented in order to better understand the distribution and projected changes in tropospheric ozone. We examine the influences of ozone precursor emissions (nitrogen oxides (NOx), carbon monoxide (CO) and volatile organic compounds (VOCs)), climate change (including methane effects) and stratospheric ozone recovery on the tropospheric ozone budget, in a simulation following the climate scenario Representative Concentration Pathway (RCP) 6.0 (a medium-high, and reasonably realistic climate scenario). Changes in ozone precursor emissions have the largest effect, leading to a global-mean increase in tropospheric ozone which maximizes in the early 21st century at 23% compared to 1960. The increase is most pronounced at northern midlatitudes, due to regional emission patterns: between 1990 and 2060, northern midlatitude tropospheric ozone remains at constantly large abundances: 31% larger than in 1960. Over this 70-year period, attempts to reduce emissions in Europe and North America do not have an effect on zonally averaged northern midlatitude ozone because of increasing emissions from Asia, together with the long lifetime of ozone in the troposphere. A simulation with fixed anthropogenic ozone precursor emissions of NOx, CO and non-methane VOCs at 1960 conditions shows a 6% increase in global-mean tropospheric ozone by the end of the 21st century, with an 11 % increase at northern midlatitudes. This increase maximizes in the 2080s and is mostly caused by methane, which maximizes in the 2080s following RCP 6.0, and plays an important role in controlling ozone directly, and indirectly through its influence on other VOCs and CO. Enhanced flux of ozone from the stratosphere to the troposphere as well as climate change-induced enhancements in lightning NOx emissions also increase the tropospheric ozone burden, although their impacts are relatively small. Overall, the results show that under this climate scenario, ozone in the future is governed largely by changes in methane and NOx; methane induces an increase in tropospheric ozone that is approximately one-third of that caused by NOx. Climate impacts on ozone through changes in tropospheric temperature, humidity and lightning NOx remain secondary compared with emission strategies relating to anthropogenic emissions of NOx, such as fossil fuel burning. Therefore, emission policies globally have a critical role to play in determining tropospheric ozone evolution through the 21st century.

Highlights

  • Ozone is a key trace gas in the atmosphere, with approximately 90 % residing in the stratosphere and 10 % in the troposphere

  • In order to understand the influences of ozone precursor emissions and climate change on the free tropospheric ozone budget, simulations were performed with the SOCOL v

  • Surface ozone in SOCOL is biased on a similar order of magnitude in the Northern Hemisphere compared with the mid-troposphere, with ozone over Europe, the US and Asia up to 20 ppb higher in 2000 compared with the ACCMIP ensemble mean (Young et al, 2013)

Read more

Summary

Introduction

Ozone is a key trace gas in the atmosphere, with approximately 90 % residing in the stratosphere and 10 % in the troposphere. Tropospheric ozone is a greenhouse gas that has contributed significantly to climate change; it has the third-highest pre-industrial to present-day radiative forcing after carbon dioxide (CO2) and methane (CH4) (Myhre et al, 2013; Stevenson et al, 2013). In addition to its roles in air pollution and climate change, tropospheric ozone is important in determining the oxidation capacity of the troposphere; the hydroxyl (OH) radical is principally produced from ozone, and controls the lifetime of many atmospheric species such as CH4, CO and NMVOCs (non-methane volatile organic compounds), including some halocarbons (Thompson, 1992)

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call