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@ARTICLE{Corsmeier:33352,
author = {Corsmeier, U. and Kalthoff, N. and Vogel, B. and Hammer,
M.-U. and Fiedler, A. R. and Kottmeier, C. and Volz-Thomas,
A. and Konrad, S. and Glaser, K. and Neininger, B. and
Lehning, M. and Jaeschke, W. and Memmesheimer, M. and
Rappenglück, B. and Jakobi, G.},
title = {{O}zone and {PAN} formation inside and outside of the
{B}erlin plume - process analysis and numerical process
simulation},
journal = {Journal of atmospheric chemistry},
volume = {42},
issn = {0167-7764},
address = {Dordrecht [u.a.]},
publisher = {Springer Science + Business Media B.V},
reportid = {PreJuSER-33352},
pages = {289 - 321},
year = {2002},
note = {Record converted from VDB: 12.11.2012},
abstract = {During the BERLIOZ field phase on 20 July 1998 a 40 km wide
ozone-plume 30 to 70 km north of Berlin in the lee of the
city was detected. The ozone mixing ratio inside the plume
was app. 15 ppb higher than outside, mainly caused by high
ozone precursor emissions in Berlin, resulting in a net
chemical ozone production of 6.5 ppb h(-1), which
overcompensates ozone advection of -3.6 ppb h(-1) and
turbulent diffusion of -1.1 ppb h(-1). That means, although
more ozone leaves the control volume far in the lee of
Berlin than enters it at the leeside cityborder and although
turbulent diffusion causes a loss of ozone in the leeside
control volume the chemical production inside the volume
leads to a net ozone increase. Using a semi-Lagrangian mass
budget method to estimate the net ozone production, 5.0 ppb
h(-1) are calculated for the plume. This means a fraction of
about $20\%$ of ozone in the plume is produced by local
emissions, therefore called 'home made' by the Berlin
emissions. For the same area KAMM/DRAIS simulations using an
observation based initialisation, results in a net
production rate between 4.0 and 6.5 ppb h(-1), while the
threefold nested EURAD model gives 6.0 ppb h(-1). The
process analysis indicates in many cases good agreement
$(10\%$ or better) between measurements and simulations not
only in the ozone concentrations but also with respect to
the physical and chemical processes governing the total
change. Remaining differences are caused by different
resolution in time and space of the models and measurements
as well as by errors in the emission calculation.The
upwind-downwind differences in PAN concentrations are partly
similar to those of ozone, because in the BERLIOZ case they
are governed mainly by photochemical production. While in
the stable boundary layer at night and windward of Berlin
0.1 to 0.3 ppb are detected, in the centre of the plume at
noon concentrations between 0.75 ppb and 1.0 ppb are
measured. The O-3/PAN ratio is about 80 to 120 and thus due
to the relatively low PAN concentrations significantly
higher than found in previous studies. The low PAN formation
on 20 July, was mainly restricted by the moderate nonmethane
hydrocarbon levels, whereas high PAN concentrations of 3.0
ppb on 21 July, are caused by local production in the
boundary layer and by large scale advection aloft.},
keywords = {J (WoSType)},
cin = {ICG-II},
ddc = {540},
cid = {I:(DE-Juel1)VDB48},
pnm = {Chemie und Dynamik der Geo-Biosphäre},
pid = {G:(DE-Juel1)FUEK257},
shelfmark = {Environmental Sciences / Meteorology $\&$ Atmospheric
Sciences},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000175947400014},
doi = {10.1023/A:1015732532499},
url = {https://juser.fz-juelich.de/record/33352},
}