4.5.1.4 Uncertainties in the tropospheric O3 budget
An updated survey of global tropospheric CTM studies since the SAR focuses
on the tropospheric O3 budget and is reported in Table
4.12. In this case authors were asked for diagnostics that did not always
appear in publication. The modelled tropospheric O3 abundances generally
agree with observations; in most cases the net budgets are in balance; and yet
the individual components vary greatly. For example, the stratospheric source
ranges from 400 to 1,400 Tg/yr, while the surface sink is only slightly more
constrained, 500 to 1,200 Tg/yr. If absolute production is diagnosed as the
reactions of HO2 and other peroxy radicals with NO, then the globally
integrated production is calculated to be very large, 2,300 to 4,300 Tg/yr and
is matched by an equally large sink (see Sections 4.2.3.3
and 4.2.6). The differences between the flux from
the stratosphere and the destruction at the surface is balanced by the net in
situ photochemical production. In this survey, the net production varies widely,
from -800 to +500 Tg/yr, indicating that in some CTMs the troposphere is a large
chemical source and in others a large sink. Nevertheless, the large differences
in the stratospheric source are apparently the driving force behind whether
a model calculates a chemical source or sink of tropospheric O3.
Individual CTM studies of the relative roles of stratospheric influx versus
tropospheric chemistry in determining the tropospheric O3 abundance
(e.g., Roelofs and Lelieveld, 1997; Wang et al., 1998a; Yienger et al., 1999)
will not represent a consensus until all CTMs develop a more accurate representation
of the stratospheric source consistent with observations (Murphy and Fahey,
1994).
Table 4.12: Tropospheric ozone budgets for circa
1990 conditions from a sample of global 3-D CTMs since the SAR. |
|
CTM |
STE
|
Prod
|
Loss
|
P-L
|
SURF
|
Burden
|
Reference |
|
|
(Tg/yr)
|
|
(Tg)
|
|
|
MATCH |
1440
|
2490
|
3300
|
-810
|
620
|
|
Crutzen et al. (1999) |
MATCH-MPIC |
1103
|
2334
|
2812
|
-478
|
621
|
|
Lawrence et al. (1999) |
ECHAM/TM3 |
768
|
3979
|
4065
|
-86
|
681
|
311
|
Houweling et al. (1998) |
ECHAM/TM3a |
740
|
2894
|
3149
|
-255
|
533
|
266
|
Houweling et al. (1998) |
HARVARD |
400
|
4100
|
3680
|
+420
|
820
|
310
|
Wang et al. (1998a) |
GCTM |
696
|
|
|
+128
|
825
|
298
|
Levy et al. (1997) |
UIO |
846
|
|
|
+295
|
1178
|
370
|
Berntsen et al. (1996) |
ECHAM4 |
459
|
3425
|
3350
|
+75
|
534
|
271
|
Roelofs and Lelieveld (1997) |
MOZARTb |
391
|
3018
|
2511
|
+507
|
898
|
193
|
Hauglustaine et al. (1998) |
STOCHEM |
432
|
4320
|
3890
|
+430
|
862
|
316
|
Stevenson et al. (2000) |
KNMI |
1429
|
2864
|
3719
|
-855
|
574
|
|
Wauben et al. (1998) |
UCI |
473
|
4229
|
3884
|
+345
|
812
|
288
|
Wild and Prather (2000) |
|
|