Abstract

Abstract. The impact of the East Asia monsoon on the seasonal behavior of O3 in the boundary layer of Eastern China and the west Pacific region was analyzed for 2004–2006 by means of full-year nested chemical transport model simulations and continuous observational data obtained from three inland mountain sites in central and eastern China and three oceanic sites in the west Pacific region. The basic common features of O3 seasonal behaviors over all the monitoring sites are the pre- and post-monsoon peaks with a summer trough. Such bimodal seasonal patterns of O3 are predominant over the region with strong summer monsoon penetration, and become weaker or even disappear outside the monsoon region. The seasonal/geographical distribution of the pre-defined monsoon index indicated that the East Asia summer monsoon is responsible for the bimodal seasonal O3 pattern, and also partly account for the differences in the O3 seasonal variations between the inland mountain and oceanic sites. Over the inland mountain sites, the O3 concentration increased gradually from the beginning of the year, reached a maximum in June, decreased rapidly to the summer valley in July or August, and then peaked in September or October, thereafter decreased gradually again. Over the oceanic sites, O3 abundance showed a similar increasing trend beginning in January, but then decreased gradually from the end of March, followed by a wide trough with the minimum in July and August and a small peak in October or November. A sensitivity analysis performed by setting China-emission to zero revealed that the chemically produced O3 from China-emission contributed substantially to the O3 abundance, particularly the pre- and post-monsoon O3 peaks, over China mainland. We found that China-emission contributed more than 40% to total boundary layer O3 during summertime (60–70% in July) and accounted for about 40 ppb of each peak value over the inland region if without considering the effect of the nonlinear chemical productions. In contrast, over the oceanic region in the high monsoon index zone, the contribution of China-emission to total boundary layer O3 was always less than 20% (<10 ppb), and less than 10% in summer.

Highlights

  • Ozone is an important trace gas in the troposphere that plays a central role in atmospheric photochemistry and has important effects on regional climates as a greenhouse gas

  • Local O3 abundance is mainly produced by the photochemical reaction from its precursors emitted from the regional polluted industrial areas; the summer minimum is primarily due to the dilution of local O3 concentration, as well as its precursors, as a result of the incursion of the clean and moist oceanic air mass carried by East Asia summer monsoon

  • Three full-year simulations for 2004–2006 were conducted with a nested CMAQ model to investigate the seasonal behavior of O3 in the boundary layer in central and eastern China and the west Pacific region

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Summary

Introduction

Ozone is an important trace gas in the troposphere that plays a central role in atmospheric photochemistry and has important effects on regional climates as a greenhouse gas. The seasonal variations of boundary layer O3 over East Asia have already been widely studied and presented a typical seasonal cycle of spring maximum-summer minimum (e.g. Wild et al, 2001; Pochanart et al, 1999, 2002, 2003; Yamaji et al, 2006). The observed summer minimum of surface O3 over East Asia was attributed to the incursion of monsoon which transports oceanic air with less O3 to the region and causes lower O3 concentration This study focused mainly on the influence of the summer monsoon on the seasonal cycle and geographic distribution of boundary layer O3 over East Asia, by the application of a normalized seasonality monsoon index, based on three years’ observational data from three inland mountain sites in central and eastern China and three oceanic monitoring stations in the west Pacific region.

Data and methods
Validation of simulated O3 by comparison with observations
Bimodal seasonal patterns of O3
O3 seasonal cycle in the high MI zone
Conclusions
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