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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 41<br />

cloud was in contact with the ground and the<br />

measuring station. Both water and ice clouds were<br />

examined at different times of the year. <strong>The</strong> second<br />

series of experiments is the CLOud Processing<br />

of regional Air Pollution advecting over land and<br />

sea (CLOPAP) series, where ageing pollution aerosol<br />

from UK cities was observed, from an airborne<br />

platform, to interact with warm stratocumulus<br />

cloud in a cloud- capped atmospheric boundary<br />

layer. Combining the results it is shown that aged<br />

pollution aerosol consists of an internal mixture<br />

of organics, sulfate, nitrate and ammonium, the<br />

organic component is dominated by highly oxidized<br />

secondary material. <strong>The</strong> relative contributions<br />

and absolute loadings of the components<br />

vary with location and season. However, these<br />

aerosols act as Cloud Condensation Nuclei (CCN)<br />

and much of the organic material, along with the<br />

other species, is incorporated into cloud droplets.<br />

In ice and mixed phase cloud, it is observed that<br />

very sharp transitions (extending over just a few<br />

metres) are present between highly glaciated regions<br />

and regions consisting of supercooled water.<br />

This is a unique. finding; however, aircraft<br />

observations in cumulus suggest that this kind of<br />

structure may be found in these cloud types too. It<br />

is suggested that this sharp transition is caused by<br />

ice nucleation initiated by oxidised organic aerosol<br />

coated with sulfate in more polluted regions<br />

of cloud, sometimes enhanced by secondary ice<br />

particle production in these regions.<br />

Faraday Discussions, 2008, V137, pp 205-222.<br />

08.1-15<br />

Limits on climate sensitivity derived from recent<br />

satellite and surface observations<br />

Chylek P, Lohmann U, Dubey M, Mishchenko M,<br />

Kahn R, Ohmura A<br />

USA, Switzerland<br />

Modelling , Meteorology & Atmospheric Sciences<br />

An analysis of satellite and surface measurements<br />

of aerosol optical depth suggests that global average<br />

of aerosol optical depth has been recently<br />

decreasing at the rate of around 0.0014/a. This<br />

decrease is nonuniform with the fastest decrease<br />

observed over the United States and Europe. <strong>The</strong><br />

observed rate of decreasing aerosol optical depth<br />

produces the top of the atmosphere radiative forcing<br />

that is comparable to forcing due to the current<br />

rate of increasing atmospheric concentration<br />

of carbon dioxide and other greenhouse gases.<br />

Consequently, both increasing atmospheric concentration<br />

of greenhouse gases and decreasing<br />

loading of atmospheric aerosols are major contributors<br />

to the top-of-atmosphere radiative forc-<br />

ing. We find that the climate sensitivity is reduced<br />

by at least a factor of 2 when direct and indirect<br />

effects of decreasing aerosols are included, compared<br />

to the case where the radiative forcing is<br />

ascribed only to increases in atmospheric concentrations<br />

of carbon dioxide. We find the empirical<br />

climate sensitivity to be between 0.29 and 0.48 K/<br />

Wm(-2) when aerosol direct and indirect radiative<br />

forcing is included.<br />

Journal of Geophysical Research Atmospheres,<br />

2007, V112, ND24, DEC 13 ARTN: D24S04.<br />

08.1-16<br />

Long-term trend analysis of aerosol variables<br />

at the high-alpine site Jungfraujoch<br />

Collaud Coen M, Weingartner E, Nyeki S, Cozic J,<br />

Henning S, Verheggen B, Gehrig R, Baltensperger U<br />

Switzerland<br />

Meteorology & Atmospheric Sciences<br />

This study reports the first long-term trend analysis<br />

of aerosol optical measurements at the highalpine<br />

site Jungfraujoch, which started 10.5 years<br />

ago. Since the aerosol variables are approximately<br />

lognormally distributed, the seasonal Kendall test<br />

and Sen’s slope estimator were applied as nonparametric<br />

methods to detect the long- term trends for<br />

each month. <strong>The</strong> yearly trend was estimated by a<br />

least-mean-square fit, and the number of years<br />

necessary to detect this trend was calculated. <strong>The</strong><br />

most significant trend is the increase (4-7% yr(-1))<br />

in light-scattering coefficients during the September<br />

to December period. <strong>The</strong> light absorption and<br />

backscattering coefficients and the aerosol number<br />

concentration also show a positive trend during<br />

this time of the year. <strong>The</strong> hemispheric backscattering<br />

fraction and the scattering exponent<br />

calculated with the smaller wavelengths (450 and<br />

550 nm), which relate to the small aerosol size<br />

fraction, decrease except during the summer,<br />

whereas the scattering exponent calculated with<br />

the larger wavelengths (550 and 700 nm) remains<br />

constant. Generally, the summer months at the<br />

Jungfraujoch, which are strongly influenced by<br />

planetary boundary layer air masses, do not show<br />

any long-term trend. <strong>The</strong> trends determined by<br />

least-mean-square fits of the scattering and backscattering<br />

coefficients, the hemispheric backscattering<br />

fractions, and the scattering exponent are<br />

significant, and the number of years necessary<br />

to detect them is shorter than 10 years. For these<br />

variables, the trends and the slopes estimated by<br />

the seasonal Kendall test are therefore confirmed<br />

by the least-mean- square fit results.<br />

Journal of Geophysical Research Atmospheres,<br />

2007, V112, ND13, JUL 13 ARTN: D13213.

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