Abstract

Abstract. We use aircraft observations obtained during the Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS) mission to examine the distributions and source attributions of O3 and NOy in the Arctic and sub-Arctic region. Using a number of marker tracers, we distinguish various air masses from the background troposphere and examine their contributions to NOx, O3, and O3 production in the Arctic troposphere. The background Arctic troposphere has a mean O3 of ~60 ppbv and NOx of ~25 pptv throughout spring and summer with CO decreasing from ~145 ppbv in spring to ~100 ppbv in summer. These observed mixing ratios are not notably different from the values measured during the 1988 ABLE-3A and the 2002 TOPSE field campaigns despite the significant changes in emissions and stratospheric ozone layer in the past two decades that influence Arctic tropospheric composition. Air masses associated with stratosphere-troposphere exchange are present throughout the mid and upper troposphere during spring and summer. These air masses, with mean O3 concentrations of 140–160 ppbv, are significant direct sources of O3 in the Arctic troposphere. In addition, air of stratospheric origin displays net O3 formation in the Arctic due to its sustainable, high NOx (75 pptv in spring and 110 pptv in summer) and NOy (~800 pptv in spring and ~1100 pptv in summer). The air masses influenced by the stratosphere sampled during ARCTAS-B also show conversion of HNO3 to PAN. This active production of PAN is the result of increased degradation of ethane in the stratosphere-troposphere mixed air mass to form CH3CHO, followed by subsequent formation of PAN under high NOx conditions. These findings imply that an adequate representation of stratospheric NOy input, in addition to stratospheric O3 influx, is essential to accurately simulate tropospheric Arctic O3, NOx and PAN in chemistry transport models. Plumes influenced by recent anthropogenic and biomass burning emissions observed during ARCTAS show highly elevated levels of hydrocarbons and NOy (mostly in the form of NOx and PAN), but do not contain O3 higher than that in the Arctic tropospheric background except some aged biomass burning plumes sampled during spring. Convection and/or lightning influences are negligible sources of O3 in the Arctic troposphere but can have significant impacts in the upper troposphere in the continental sub-Arctic during summer.

Highlights

  • Tropospheric ozone (O3) is important as it affects air quality and is a greenhouse gas

  • The CO ∼ 120 ppbv threshold during Aircraft and Satellites (ARCTAS)-B is chosen based on the probability density function (PDF) of CO (Sect. 3). d The CH3CN ∼ 145 pptv for ARCTAS-A and ∼320 pptv for ARCTAS-B thresholds are chosen for the optimal segregation between the biomass burning and anthropogenic pollutions based on the CO2/CO, CH4/CO, and C2H6/CO ratio

  • The thresholds of CH3CN ∼145 pptv for ARCTASA and ∼320 pptv for ARCTAS-B are chosen for optimal segregation between the biomass burning and anthropogenic pollutions based on the CO2/CO, CH4/CO, and C2H6/CO ratios (Table 2), which differ in these two types of air masses

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Summary

Introduction

Tropospheric ozone (O3) is important as it affects air quality and is a greenhouse gas. While increases in long-lived greenhouse gases dominate Arctic warming, O3 and other short-lived pollutants (e.g., aerosols) could play an important role (Law and Stohl, 2007; Shindell, 2007; Quinn et al, 2008). Stratospheric air contains high NOx and nitric acid (HNO3) and is an important source of NOxwhen injected into the Arctic troposphere (Wofsy et al, 1992; Levy et al, 1999; Law and Stohl, 2007; Liang et al, 2009). A better quantification of the contribution of various anthropogenic and natural sources to O3 in the Arctic is important for understanding the temporal variation and radiative impact of O3, and how Arctic O3 may change as climate warms and the stratospheric O3 layer recovers.

Observations and model
Instrument & Methods
Air sampled during ARCTAS
Air mass identification
Background
Air mass composition
Reactive nitrogen in the Arctic troposphere
Reactive nitrogen in various air masses
PAN in air masses influenced by STE
Ozone and ozone production in the Arctic troposphere
Dependence of ozone production on NOx and HOx
O3 and O3 production in various air masses
Findings
Conclusions
Full Text
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