Ozone stratospheric injection into troposphere

As discussed in other chapters of this book and summarized in Chapter 16, the formation of tropospheric ozone from photochemical reactions of volatile organic compounds (VOC) and oxides of nitrogen (NC/) involves many reactions. Concentrations are therefore quite variable geographically, temporally, and altitudinally. Additional complications come from the fact that there are episodic injections of stratospheric 03 into the troposphere as well as a number of sinks for its removal. Because 03 decomposes thermally, particularly on surfaces, it is not preserved in ice cores. All of these factors make the development of a global climatology for 03 in a manner similar to that for N20 and CH4, for example, much more difficult. In addition, the complexity of the chemistry leading to O, formation from VOC and NOx is such that model-predicted ozone concentrations can vary from model to model (e.g., see Olson et al., 1997). 

Photochemical air pollution in the troposphere results from a complex interplay between sunlight and primary air pollutants emitted in ambient air that leads to the formation of ozone and other oxidizing and cye-irritaling agents. On the other hand, pollutants injected into the stratosphere by such human activities as supersonic transports (SST s) and release ofchlorofiuoro-methancs in air by their use as aerosol propellants and refrigerants may eventually reduce the protective layer of ozone from harsh solar ultraviolet radiation. Although the full impact of injected air pollutants in the stratosphere is not apparent at present, various model calculations show conclusively that the continuous future release of chlorofluoromethanes and NO (NO and N02) would result in substantial reduction of ozone in the stratosphere. 

As the residence time of aerosols in the stratosphere is 2 yr and in the troposphere 1 week, the Be/ Be ratio of the two air masses is distinctive. Tropospheric air shows the ratio of Be relative to Be of 1.8, whereas stratospheric air has a ratio of 0.13. It is therefore possible to distinguish stratospheric air injected into the troposphere by considering the ratio of Be/ Be. Of course, the stratospheric air will also be higher in Be than the tropospheric air. As stratospheric air will also contain ozone, the interest in this source has been strong to distinguish from pollution-based tropospheric ozone. 

---