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 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.