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Aviation and the Global Atmosphere

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<strong>Aviation</strong> <strong>and</strong> <strong>the</strong> <strong>Global</strong> <strong>Atmosphere</strong><br />

One study of <strong>the</strong> effect of increasing CO 2 amounts (Pitari <strong>and</strong> Visconti, 1994) showed that<br />

stratospheric cooling mitigated <strong>the</strong> increase in NO x . However, this study did not take into<br />

consideration <strong>the</strong> increase in H 2 O associated with aircraft; <strong>the</strong>refore, more complete studies<br />

need to be done with a wide range of models.<br />

Ano<strong>the</strong>r major uncertainty regarding knowledge of <strong>the</strong> future stratosphere is that associated<br />

with source gases, in particular H 2 O. This uncertainty is underscored by our lack of<br />

underst<strong>and</strong>ing of current H 2 O trends. <strong>Global</strong> trends in stratospheric humidity over <strong>the</strong> period<br />

1992 to 1996 inclusive have been presented recently by Evans et al. (1998) using Upper<br />

<strong>Atmosphere</strong> Research Satellite (UARS) measurements of H 2 O <strong>and</strong> CH 4 from <strong>the</strong> Halogen<br />

Occultation Experiment (HALOE) instrument. The authors find that <strong>the</strong> combined budget of<br />

2CH 4 + H 2 O is approximately constant with altitude <strong>and</strong> is increasing with a global mean<br />

value of 61 ppbv yr-1 . A more local view of water vapor increase in <strong>the</strong> lower stratosphere<br />

was presented by Oltmans <strong>and</strong> Hofmann (1995) over <strong>the</strong> period 1981 to 1994. They found a<br />

maximum rate of increase in <strong>the</strong> 18-20 km layer of 32 ppbv yr-1 . The rate of increase of H2O observed in <strong>the</strong> stratosphere is greater than <strong>the</strong> increase in tropospheric CH4 . One<br />

suggestion is that <strong>the</strong> increase could be accounted for by a change in tropopause<br />

temperature of a few tenths of a degree, <strong>and</strong> <strong>the</strong> most recent changes might be a result of<br />

changes in <strong>the</strong> dynamics of <strong>the</strong> tropics induced by heating of Mt. Pinatubo aerosols<br />

(Schauffer <strong>and</strong> Daniel, 1994). This uncertainty highlights <strong>the</strong> delicate balance between<br />

chemistry <strong>and</strong> climate.<br />

4.4.3. Soot Emissions by Subsonic <strong>and</strong> Supersonic Aircraft<br />

The chemistry of<br />

soot has been<br />

discussed in<br />

Chapter 2; <strong>the</strong><br />

conclusion is that<br />

it does not react<br />

with O 3 in a<br />

catalytic manner.<br />

That is, O 3 can<br />

be destroyed by<br />

soot, but <strong>the</strong> soot<br />

is consumed in<br />

<strong>the</strong> process (see<br />

Section 2.1.3.1).<br />

http://www.ipcc.ch/ipccreports/sres/aviation/051.htm (8 von 10)08.05.2008 02:42:31<br />

Figure 4-11: Ozone column (left panels) <strong>and</strong> ozone profile (right<br />

panels) percentage difference as a function of latitude <strong>and</strong> month for<br />

three models <strong>and</strong> three supersonic aircraft scenarios with respect to<br />

scenario D: UNIVAQ-2D model for S1c; AER-2D model for S1k; <strong>and</strong><br />

GSFC-2D model for S1h. This figure mainly illustrates model<br />

differences ra<strong>the</strong>r than scenario differences.

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