Global Change Abstracts The Swiss Contribution - SCNAT
Global Change Abstracts The Swiss Contribution - SCNAT
Global Change Abstracts The Swiss Contribution - SCNAT
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<strong>Global</strong> <strong>Change</strong> <strong>Abstracts</strong> – <strong>The</strong> <strong>Swiss</strong> <strong>Contribution</strong> | Atmosphere 59<br />
the underlying rocks and the relatively high permeability<br />
of soils which reduce the ‘hydrological<br />
memory’ of the soil cover in the mountain basins<br />
investigated.<br />
Quarterly Journal of the Royal Meteorological Society,<br />
2007, V133, N625, B, APR, pp 867-880.<br />
08.1-59<br />
Ice nucleation of ammonia gas exposed montmorillonite<br />
mineral dust particles<br />
Salam A, Lohmann U, Lesins G<br />
Canada, Bangladesh, Switzerland<br />
Meteorology & Atmospheric Sciences<br />
<strong>The</strong> ice nucleation characteristics of montmorillonite<br />
mineral dust aerosols with and without<br />
exposure to ammonia gas were measured at different<br />
atmospheric temperatures and relative humidities<br />
with a continuous flow diffusion chamber.<br />
<strong>The</strong> montmorillonite particles were exposed<br />
to pure (100%) and diluted ammonia gas (25 ppm)<br />
at room temperature in a stainless steel chamber.<br />
<strong>The</strong>re was no significant change in the mineral<br />
dust particle size distribution due to the ammonia<br />
gas exposure. 100% pure ammonia gas exposure<br />
enhanced the ice nucleating fraction of montmorillonite<br />
mineral dust particles 3 to 8 times at<br />
90% relative humidity with respect to water (RHw)<br />
and 5 to 8 times at 100% RHw for 120 min exposure<br />
time compared to unexposed montmorillonite<br />
within our experimental conditions. <strong>The</strong><br />
percentages of active ice nuclei were 2 to 8 times<br />
higher at 90% RHw and 2 to 7 times higher at 100%<br />
RHw in 25 ppm ammonia exposed montmorillonite<br />
compared to unexposed montmorillonite. All<br />
montmorillonite particles are more efficient as ice<br />
nuclei with increasing relative humidities and decreasing<br />
temperatures. <strong>The</strong> activation temperature<br />
of montmorillonite exposed to 100% pure ammonia<br />
was 15 degrees C higher than for unexposed<br />
montmorillonite particles at 90% RHw. In the 25<br />
ppm ammonia exposed montmorillonite experiments,<br />
the activation temperature was 10 degrees<br />
C warmer than unexposed montmorillonite at 90%<br />
RHw. Degassing does not reverse the ice nucleating<br />
ability of ammonia exposed montmorillonite<br />
mineral dust particles suggesting that the ammonia<br />
is chemically bound to the montmorillonite<br />
particle. This is the first experimental evidence<br />
that ammonia gas exposed montmorillonite mineral<br />
dust particles can enhance its activation as ice<br />
nuclei and that the activation can occur at temperatures<br />
warmer than -degrees C where natural<br />
atmospheric ice nuclei are very scarce.<br />
Atmospheric Chemistry and Physics, 2007, V7,<br />
N14, pp 3923-3931.<br />
08.1-60<br />
A trajectory-based estimate of the tropospheric<br />
ozone column using the residual method<br />
Schoeberl M R, Ziemke J R, Bojkov B, Livesey N J,<br />
Duncan B, Strahan S, Froidevaux L, Kulawik S, Bhartia<br />
P K, Chandra S, Levelt P F, Witte J C, Thompson A<br />
M, Cuevas E, Redondas A, Tarasick D W, Davies J,<br />
Bodeker G E, Hansen G, Johnson B J, Oltmans S J,<br />
Voemel H, Allaart M, Kelder H, Newchurch M, Godin<br />
Beekmann S, Ancellet G, Claude H, Andersen S B,<br />
Kyroe E, Parrondos M C, Yela M, Zablocki G, Moore<br />
D, Dier H, von der Gathen P, Viatte P, Stuebi R, Calpini<br />
B, Skrivankova P, Dorokhov V, de Backer H, Schmidlin<br />
F J, Coetzee G, Fujiwara M, Thouret V, Posny F, Morris<br />
G, Merrill J, Leong C P, König Langlo G, Joseph E<br />
USA, Netherlands, Spain, Canada, New Zealand,<br />
Norway, France, Denmark, Finland, Poland, England,<br />
Germany, Switzerland, Czech Republic, Russia,<br />
Belgium, South Africa, Japan, Malaysia<br />
Meteorology & Atmospheric Sciences , Modelling<br />
We estimate the tropospheric column ozone using<br />
a forward trajectory model to increase the<br />
horizontal resolution of the Aura Microwave<br />
Limb Sounder (MLS) derived stratospheric column<br />
ozone. Subtracting the MLS stratospheric column<br />
from Ozone Monitoring Instrument total column<br />
measurements gives the trajectory enhanced tropospheric<br />
ozone residual (TTOR). Because of different<br />
tropopause definitions, we validate the basic<br />
residual technique by computing the 200-hPato-<br />
surface column and comparing it to the same<br />
product from ozonesondes and Tropospheric<br />
Emission Spectrometer measurements. Comparisons<br />
show good agreement in the tropics and reasonable<br />
agreement at middle latitudes, but there<br />
is a persistent low bias in the TTOR that may be<br />
due to a slight high bias in MLS stratospheric column.<br />
With the improved stratospheric column<br />
resolution, we note a strong correlation of extratropical<br />
tropospheric ozone column anomalies<br />
with probable troposphere-stratosphere exchange<br />
events or folds. <strong>The</strong> folds can be identified by their<br />
colocation with strong horizontal tropopause gradients.<br />
TTOR anomalies due to folds may be mistaken<br />
for pollution events since folds often occur<br />
in the Atlantic and Pacific pollution corridors.<br />
We also compare the 200-hPa-to-surface column<br />
with <strong>Global</strong> Modeling Initiative chemical model<br />
estimates of the same quantity. While the tropical<br />
comparisons are good, we note that chemical<br />
model variations in 200hPa-to-surface column at<br />
middle latitudes are much smaller than seen in<br />
the TTOR.<br />
Journal of Geophysical Research Atmospheres,<br />
2007, V112, ND24, DEC 19 ARTN: D24S49.