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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.

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