Abstract

Simulations by six CMIP6 Earth System Models indicate that the seasonal cycle of baseline tropospheric ozone at northern midlatitudes has been shifting since the mid-20th Century. Beginning in ~ 1940 the seasonal cycle increased in amplitude by ~ 10 ppb (measured from seasonal minimum to maximum), and the seasonal maximum shifted to later in the year by about 3 weeks. This shift maximized in the mid-1980s, followed by a reversal – the seasonal cycle decreased in amplitude and the maximum shifted back to earlier in the year. Similar changes are seen in measurements collected from the 1970s to the present. The timing of the seasonal cycle changes is generally concurrent with the rise and fall of anthropogenic emissions that followed industrialization and subsequent implementation of air quality emission controls. We quantitatively compare the temporal changes of the ozone seasonal cycle at sites in both Europe and North America with the temporal changes of ozone precursor emissions across the northern midlatitudes and find a high degree of similarity between these two temporal patterns. We hypothesize that changing precursor emissions are responsible for the shift in the ozone seasonal cycle, and suggest the mechanism by which changing emissions drive the changing seasonal cycle: increasing emissions of NOX allow summertime photochemical production of ozone to become more important than ozone transported from the stratosphere and increasing VOCs lead to progressively greater photochemical ozone production in the summer months, thereby increasing the amplitude of the seasonal ozone cycle. Decreasing emissions of both precursor classes then reverse these changes. The quantitative parameter values that characterize the seasonal shifts provide useful benchmarks for evaluating model simulations, both against observations and between models.

Highlights

  • Tropospheric ozone is a harmful air pollutant and greenhouse gas

  • We obtained monthly mean ozone concentrations for all six Earth System Models (ESMs) at the model levels that correspond to the selected comparison locations

  • The time series considered here span a maximum of 165 years, which allows significant influence from “longer-term” variations driven by ozone precursor emission changes and climate variations

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Summary

Introduction

Tropospheric ozone is a harmful air pollutant and greenhouse gas. It is a secondary pollutant, formed as a photochemical35 product of oxidation reactions involving volatile organic compounds (VOCs), carbon monoxide (CO), and methane (CH4) in the presence of oxides of nitrogen (NOX). Tropospheric ozone is a harmful air pollutant and greenhouse gas. It is a secondary pollutant, formed as a photochemical. Another consequence of rapid transport of ozone and its precursors is that emissions from any location in the northern midlatitude region can influence

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