Abstract
Abstract. The relationship between springtime air pollution transport of ozone (O3) and carbon monoxide (CO) and mid-latitude cyclones is explored for the first time using the Monitoring Atmospheric Composition and Climate (MACC) reanalysis for the period 2003–2012. In this study, the most intense spring storms (95th percentile) are selected for two regions, the North Pacific (NP) and the North Atlantic (NA). These storms (∼60 storms over each region) often track over the major emission sources of East Asia and eastern North America. By compositing the storms, the distributions of O3 and CO within a "typical" intense storm are examined. We compare the storm-centered composite to background composites of "average conditions" created by sampling the reanalysis data of the previous year to the storm locations. Mid-latitude storms are found to redistribute concentrations of O3 and CO horizontally and vertically throughout the storm. This is clearly shown to occur through two main mechanisms: (1) vertical lifting of CO-rich and O3-poor air isentropically, from near the surface to the mid- to upper-troposphere in the region of the warm conveyor belt; and (2) descent of O3-rich and CO-poor air isentropically in the vicinity of the dry intrusion, from the stratosphere toward the mid-troposphere. This can be seen in the composite storm's life cycle as the storm intensifies, with area-averaged O3 (CO) increasing (decreasing) between 200 and 500 hPa. The influence of the storm dynamics compared to the background environment on the composition within an area around the storm center at the time of maximum intensity is as follows. Area-averaged O3 at 300 hPa is enhanced by 50 and 36% and by 11 and 7.6% at 500 hPa for the NP and NA regions, respectively. In contrast, area-averaged CO at 300 hPa decreases by 12% for NP and 5.5% for NA, and area-averaged CO at 500 hPa decreases by 2.4% for NP while there is little change over the NA region. From the mid-troposphere, O3-rich air is clearly seen to be transported toward the surface, but the downward transport of CO-poor air is not discernible due to the high levels of CO in the lower troposphere. Area-averaged O3 is slightly higher at 1000 hPa (3.5 and 1.8% for the NP and NA regions, respectively). There is an increase of CO at 1000 hPa for the NP region (3.3%) relative to the background composite and a~slight decrease in area-averaged CO for the NA region at 1000 hPa (-2.7%).
Highlights
Tropospheric ozone (O3) and carbon monoxide (CO) are relatively long-lived air pollutants, especially when in the free troposphere (Monks et al, 2009)
The individual storm tracks for the 95th percentile MAM storms over the North Pacific (NP) (62 storms) and North Atlantic (NA) (58 storms) regions are shown in Fig. 1a and b
These intense storms are located in the major storm track pathways, generally having originated over eastern China or east of the Rocky Mountains, and track northeast with the location of maximum ζ850 typically occurring over the remote ocean
Summary
Tropospheric ozone (O3) and carbon monoxide (CO) are relatively long-lived air pollutants, especially when in the free troposphere (Monks et al, 2009). O3 is photochemically produced from both anthropogenic precursor sources (CO and nitrogen oxides (NOx=NO + NO2)) and natural precursor sources (e.g., NOx from lightning and soils, and volatile organic carbons (VOCs) in the presence of NOx). Production of CO is the result of incomplete combustion of fossil fuel and biomass burning, as well as the oxidation of VOCs (Holloway et al, 2000; Kumar et al, 2013). Meteorological conditions play an important role in the intercontinental transport of pollutants. Air in the boundary layer mixes with the rest of the troposphere by frontal lifting or convection
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