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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 />

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

Table of contents | Previous page | Next page<br />

2.2.2. Observing Changes in Atmospheric Ozone from Present <strong>Aviation</strong><br />

2.2.2.1. Observed Ozone Trends in <strong>the</strong> Upper Troposphere <strong>and</strong> Lower Stratosphere<br />

O<strong>the</strong>r reports in this collection<br />

A decreasing trend in stratospheric ozone has been a pivotal diagnostic in <strong>the</strong> assessment of anthropogenic halocarbon release. Because <strong>the</strong> bulk of global ozone<br />

resides in <strong>the</strong> stratosphere, measurements of total column ozone-which can be made quite accurately-have served as a proxy for stratospheric ozone abundance.<br />

Downward trends in total ozone are now well-established throughout all seasons <strong>and</strong> all latitudes, except in <strong>the</strong> tropics (WMO-UNEP, 1999). Broad agreement on <strong>the</strong><br />

magnitude of <strong>the</strong> total ozone trend exists between ground-based <strong>and</strong> satellite observational databases <strong>and</strong> model predictions based on chlorine-catalyzed ozone<br />

destruction. However, as discussed in Section 2.1, aircraft engine emissions may induce changes of different magnitude <strong>and</strong>/or sign in tropospheric <strong>and</strong> stratospheric<br />

ozone densities. Therefore, to observe possible effects of aviation on <strong>the</strong> ozone layer, one is likely to have to focus on trends in <strong>the</strong> vertical ozone profile ra<strong>the</strong>r than<br />

overall column abundance.<br />

Natural phenomena such as volcanic eruptions <strong>and</strong> seasonal <strong>and</strong> interannual climate variations may affect ozone density variations in <strong>the</strong> UT <strong>and</strong> LS. The time<br />

constants associated with <strong>the</strong>se phenomena range from months (in <strong>the</strong> case of short-term climate variation) to years (for <strong>the</strong> occasional volcanic eruption) to possibly<br />

decades (for long-term climate change). Because extensive observational data on ozone are limited to <strong>the</strong> past several decades, it is not possible to completely<br />

deconvolute <strong>the</strong> impacts of various natural phenomena. The data record is sufficiently long, however, to allow characterization of periodic phenomena occuring on<br />

shorter time scales. Most of <strong>the</strong> anthropogenic forcings have been increasing secularly during <strong>the</strong> period of observation. Consequently, attempts to discriminate trend<br />

components can be carried out only with <strong>the</strong> aid of model predictions for each forcing.<br />

Trend analyses of vertical ozone profiles have become possible only during <strong>the</strong> 1980s <strong>and</strong> 1990s as a result of data from <strong>the</strong> ground-based (Umkehr technique) <strong>and</strong><br />

ozonesonde networks, <strong>and</strong> satellite-borne solar backscatter ultraviolet spectrometer (SBUV) <strong>and</strong> Stratospheric Aerosol <strong>and</strong> Gas Experiment (SAGE) I/II instruments<br />

(Logan, 1994; Miller et al.,1995; WMO-UNEP, 1995; Fortuin <strong>and</strong> Kelder, 1997; Harris et al., 1997; WMO, 1998; see also Figure 2-4). The middle stratospheric trends<br />

derived from different data sets show broad agreement with each o<strong>the</strong>r. The negative trend peaking at ~40-km altitude <strong>and</strong> extending from 30 to 50 km in middle<br />

latitudes is ascribed to <strong>the</strong> simple Cl-ClO catalytic cycle of ozone destruction from enhanced atmospheric chlorine loading. A significant negative trend is also<br />

discerned in <strong>the</strong> lowermost stratosphere (i.e., between <strong>the</strong> troposphere <strong>and</strong> approximately 20-km altitude), where increased heterogeneous conversion of chlorinecontaining<br />

reservoir species to reactive radical forms has been suggested as a factor in ozone destruction through catalytic cycles involving <strong>the</strong> ClO+ClO <strong>and</strong> ClO+BrO<br />

reactions.<br />

http://www.ipcc.ch/ipccreports/sres/aviation/027.htm (1 von 3)08.05.2008 02:41:45

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