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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 />

scale wea<strong>the</strong>r systems. An estimate of annual flux into <strong>the</strong> free troposphere from European surface NO x sources, as a fraction of <strong>the</strong> total surface NO x source, can be<br />

made from European Monitoring <strong>and</strong> Evaluation Program (EMEP) modeling studies (Tuovinen et al., 1994). For NO x , 52% of <strong>the</strong> emitted NO x was deposited within <strong>the</strong><br />

EMEP area of Europe <strong>and</strong> 48% was exported out of <strong>the</strong> model region during 1985-93. Approximately half of this material is vented into <strong>the</strong> free troposphere as NOy<br />

(1.7 Tg N yr -1 ), with <strong>the</strong> remainder deposited elsewhere, without reaching <strong>the</strong> free troposphere.<br />

In North America, a similar picture applies. Model calculations (Brost et al., 1988) have estimated that about 1.8 Tg yr-1 (of total North American emissions of 7.9 Tg N<br />

yr-1 ) is transported east to <strong>the</strong> Atlantic Ocean between <strong>the</strong> surface <strong>and</strong> 5.5-km altitude. That is, about 25% of <strong>the</strong> North American NOx emissions remained airborne in<br />

<strong>the</strong> boundary layer or free troposphere as <strong>the</strong> air left North America. More recent studies (Jacob et al., 1993; Horowitz et al., 1998; Liang et al., 1998) have derived a<br />

lower estimate of <strong>the</strong> transport out of North America (on <strong>the</strong> order of 6%).<br />

A detailed model study of advective <strong>and</strong> convective venting of ozone, NOx , <strong>and</strong> NOY out of <strong>the</strong> boundary layer over northwest Europe during July <strong>and</strong> October-<br />

November 1991 showed that, of surface NOx emissions, 7% were brought to <strong>the</strong> free troposphere as NOx <strong>and</strong> 20% as NOy during <strong>the</strong> summer (Flatoy <strong>and</strong> Hov, 1996),<br />

with slightly smaller percentages during <strong>the</strong> fall.<br />

Transport from <strong>the</strong> surface is <strong>the</strong>refore undoubtedly an important contributor to background NOx . However, it is difficult to evaluate how well this process is h<strong>and</strong>led in<br />

each of <strong>the</strong> tropospheric assessment models used for aviation impact calculations.<br />

Lightning is an important NOx source in <strong>the</strong> UT (Chameides et al., 1987; Lamarque et al., 1996). Because of its sporadic nature <strong>and</strong> small spatial scale (tens of km), it<br />

is exceedingly difficult to represent quantitatively in even <strong>the</strong> most complex of tropospheric models. Most model studies include some representation of lightning NOx ,<br />

with global total emissions in <strong>the</strong> range 1-10 Tg N yr-1 . However, <strong>the</strong>re is no consensus on how to represent this source with time of day, season, altitude, or spatially,<br />

nor how to treat lightning in concert with convection, cloud processing, <strong>and</strong> wet scavenging.<br />

Stratospheric NOy is a fur<strong>the</strong>r important source of NOx in <strong>the</strong> UT <strong>and</strong> LS, through <strong>the</strong> photolysis of HNO3 (Murphy et al., 1993). There is a downward flux of NOy from<br />

<strong>the</strong> stratosphere to <strong>the</strong> troposphere that globally balances <strong>the</strong> stratospheric NOx source produced by <strong>the</strong> reaction of N2O with O(1D). Few model studies of aircraft NOx emissions extend high enough in altitude to include a full treatment of stratospheric NOx <strong>and</strong> NOy. Moreover, most do not include an explicit representation of<br />

stratospheric chemistry (i.e., halogen chemistry) from which to realistically calculate stratospheric NOx . Instead, most models use a constant ratio of NOy to ozone <strong>and</strong><br />

describe <strong>the</strong> stratospheric NOy source in <strong>the</strong> same way as <strong>the</strong> stratosphere-troposphere exchange of ozone. Typical ozone to NOy ratios are assumed to be about<br />

1000:1, giving a stratospheric NOy source in <strong>the</strong> UT of about 0.5 Tg N yr-1 .<br />

Although <strong>the</strong> issue of <strong>the</strong> magnitude of background NO x levels has been clearly identified <strong>and</strong> much<br />

work has been performed to characterize surface, lightning, <strong>and</strong> stratospheric sources, <strong>the</strong>re are still<br />

too few measurements of NO x <strong>and</strong> NOy in <strong>the</strong> UT <strong>and</strong> LS with which to assess quantitatively<br />

representations of background NO x in <strong>the</strong> models summarized in Table 2-1. Recently published data<br />

(Emmons et al., 1997) have begun to be used for evaluation of model performance (Wang et al.,<br />

1998b).<br />

http://www.ipcc.ch/ipccreports/sres/aviation/028.htm (3 von 11)08.05.2008 02:41:47

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