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aktualisiertes pdf - DPG-Tagungen

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UP 2 Atmosphäre und Klima I<br />

Zeit: Montag 14:15–16:00 Raum: HS 118<br />

Fachvortrag UP 2.1 Mo 14:15 HS 118<br />

Airborne Lidar Measurements of Water Vapour and Humidity<br />

Fluxes during the International H2O Project 2002<br />

— •Christoph Kiemle 1 , Andreas Fix 1 , Harald Flentje 1 ,<br />

Gorazd Poberaj 1 , Martin Wirth 1 , Gerhard Ehret 1 , Michael<br />

Hardesty 2 , and Alan Brewer 2 — 1 Institut fuer Physik der Atmosphaere,<br />

Deutsches Zentrum fuer Luft- und Raumfahrt (DLR), D82234<br />

Oberpfaffenhofen — 2 NOAA Environmental Technical Laboratory, 325<br />

Broadway, Boulder, CO 80305, USA<br />

During the International H2O Project (IHOP 2002) DLR’s 100 Hz<br />

airborne differential absorption lidar (DIAL) enabled two-dimensional<br />

scans of small-scale humidity structures in the boundary layer with unprecedented<br />

spatial resolution. At an aircraft speed of 140 m/s the spatial<br />

(horizontal and vertical) resolution in the humidity field for typical<br />

daytime measurements is 200 m, accepting an average random error of<br />

10 percent. For the first time the DLR DIAL was flown together with<br />

NOAA’s high resolution Doppler lidar (HRDL), both systems pointing<br />

vertically downwards. The dominant turbulent structures of the boundary<br />

layer are well sampled by both lidars. Applying the eddy covariance<br />

technique to both data sets, the upward humidity flux within a cloud-free<br />

convective boundary layer over south-western Kansas was estimated to<br />

0.2+-0.04 g/kg m/s, which corresponds to a latent heat flux of 500+-100<br />

W/m2. The flux is found to be nearly constant with height, i.e. the flux<br />

divergence is zero, the mean boundary layer humidity is constant over<br />

time and the surface evaporation flux equals the entrainment flux at the<br />

boundary layer top, corresponding to the boundary layer growth.<br />

Fachvortrag UP 2.2 Mo 14:30 HS 118<br />

Active Groundbased DOAS-Measurements Of HCHO, NO2<br />

And O3 During FORMAT-Campaigns I And II (Summer<br />

02/03), Milan (Italy) — •Claudia Hak 1 , Achim Bäuerle 1 , Kai-<br />

Uwe Mettendorf 1 , Sebastian Trick 1 , Rainer Volkamer 1,2 ,<br />

Ulrich Platt 1 , and Irene Pundt 1 — 1 Institut für Umweltphysik der<br />

Universität Heidelberg, Im Neuenheimer Feld 229, D-69120 Heidelberg<br />

— 2 now at Massachusetts Institute of Technology, Cambridge, USA<br />

Longpath-DOAS-measurements of formaldehyde (HCHO) and other<br />

pollutants were performed during two field campaigns in the Milan area<br />

(Italy). The campaigns were part of the European project FORMAT<br />

(FORMaldehyde As a Tracer of photooxidation in the troposphere) and<br />

took place in Bresso, in the urban periphery of Milan, and in Alzate, a<br />

village located in a rural area 35 km north of Milan. The covered time<br />

period was 22.07. - 20.08.2002 and 12.09. - 05.10.2003, respectively.<br />

The main aims of the project are to obtain a better knowledge of the<br />

chemistry and distribution of HCHO in the troposphere and the improvement<br />

of analysis techniques for the measurement of formaldehyde. As one<br />

of the largest urban and industrial regions in Europe the metropolitan<br />

area of Milan was chosen. In this area, both pollutant emissions and solar<br />

radiation are high during summer - so HCHO can be photochemically<br />

produced and directly emitted. Here, comparisons of the chemical compositions<br />

of the air of both measurement sites will be shown. The mixing<br />

ratios of the photochemical constituents HCHO, NO2, and O3 during<br />

both observed time spans are studied in consideration of the meteorological<br />

conditions.<br />

Fachvortrag UP 2.3 Mo 14:45 HS 118<br />

The ECHO project intercomparison of different systems for organic<br />

trace gas measurements — •Christoph Holzke 1 and intercomparison<br />

team ECHO 2 — 1 Institut fuer Chemie und Dynamik<br />

der Geosphaere, Institut II: Troposphaere (ICG-II), Forschungszentrum<br />

Juelich, D-52425 Juelich, Germany — 2 different paticipating institutes<br />

Despite their importance for atmospheric chemistry, there is still a large<br />

uncertainty about the exact amount of biogenic VOC (Volatile Organic<br />

Compound) emissions and their contribution to tropospheric chemistry.<br />

The analysis of VOCs in ambient air is a difficult task because of the methodical<br />

complexity. This is one reason for the uncertainties in the quantification<br />

of these emissions. In this paper we present the results of two<br />

intercalibration experiments that were conducted as part of the quality<br />

assurance within the ECHO project (Emission and Chemical Transformation<br />

of Biogenic Volatile Organic Compounds). Since many biogenic<br />

VOCs are not stable in gas cylinders as used for round robin tests, the<br />

intercalibration experiments were done on site in the laboratory. We set<br />

151<br />

up a permeation source to produce a constant flow of a complex mixture<br />

of VOCs with mixing ratios in the range of ppt to ppb. The experiments<br />

focussed on the intercomparison of the quantification of specific biogenic<br />

VOCs and some of their degradation products. The intercomparison covered<br />

the following analytical systems: one on-line GC/FID, two on-line<br />

GC/MS, three off-line GC/MS, one off-line GC/FID/MS (off-line sampling<br />

on adsorption tubes), and four PTR-MS. The time resolution of<br />

the different systems was in the range of 40 minutes to 10 seconds.<br />

Fachvortrag UP 2.4 Mo 15:00 HS 118<br />

Commissioning of the new Ground-Based Microwave Radiometer<br />

RAMAS at Summit, Greenland — •Sven Golchert 1 ,<br />

Axel Kleindienst 1 , Nicole Buschmann 1 , Klaus Künzi 1 , Justus<br />

Notholt 1 , Jérôme de La Noë 2 , Nicola Schneider 2 , Helge<br />

Jønch-Sørensen 3 , Allan Gross 3 , Marianne Sloth 3 , Martyn<br />

Chipperfield 4 , and Steve Arnold 4 — 1 Institut für Umweltphysik,<br />

Universität Bremen, Germany — 2 Observatoire de Bordeaux, Université<br />

Bordeaux 1, France — 3 Danmarks Meteorologiske Institut, Københaven,<br />

Denmark — 4 Institute for Atmospheric Science, University of Leeds,<br />

UK<br />

The new microwave Radiometer for Atmospheric Measurements at<br />

Summit (RAMAS) has taken up preliminary operation at Summit,<br />

Greenland, and is now being prepared for continuous measurements.<br />

RAMAS covers the frequency band from 265 GHz to 280 GHz with an<br />

instantaneous bandwidth of currently 1 GHz. It utilises an SIS/HEMT<br />

mixer-preamplifier to minimise receiver noise. Tropospheric water vapour<br />

content, a major constraint on ground-based microwave radiometry, is exceptionally<br />

low at Summit station (72 ◦ N, 38 ◦ W, 3200 m). This for the<br />

first time in the Arctic will allow for year-round measurements and even<br />

the observation of short-term variations of less pronounced species. The<br />

principal objective of RAMAS is to measure O3, ClO, N2O and HNO3.<br />

This comprises a set of primary species involved in polar ozone chemistry,<br />

and an important dynamical tracer, which will allow for the separation<br />

of chemical and dynamical effects on O3. We present an overview of the<br />

instrument performance in its primary observation goals and first results<br />

about the feasibility of measurements of further species.<br />

Fachvortrag UP 2.5 Mo 15:15 HS 118<br />

Atmospheric carbon dioxide retrieved from ground-based solar<br />

FT-spectroscopy — •Thorsten Warneke 1 , Justus Notholt 1 ,<br />

Astrid Schulz 2 , Voltaire Velazco 1 , and Otto Schrems 2 —<br />

1 Institute of environmental physics, Uni Bremen, Bremen — 2 Alfred Wegener<br />

Institute, Bremerhaven<br />

The spatial distribution and temporal variability of the carbon sources<br />

and sinks is still uncertain and needs to be better quantified for the<br />

prediction of future climate. The measurement of column averaged volume<br />

mixing ratios from the ground is important for the validation of<br />

proposed space-borne CO2-measurements and to provide input data for<br />

inverse models. Ground-based FT-solar absorption spectra in the near<br />

infrared are obtained in Spitsbergen and during two cruises onboard the<br />

research vessel Polarstern on the Atlantic between 50N and 40S. Column<br />

averaged volume mixing ratios and a two layer profile are retrieved. The<br />

precisions of the column averaged volume mixing ratios are better than<br />

0.5<br />

Fachvortrag UP 2.6 Mo 15:30 HS 118<br />

Sauerstoff-A-Banden Messungen zur Bestimmung von Photonenweglängenverteilungen<br />

— •Thomas Scholl, Klaus Pfeilsticker<br />

und Ulrich Platt — Institut für Umweltphysik, Universität<br />

Heidelberg, Im Neuenheimer Feld 229, 69120 Heidelberg<br />

Hochauflösende spektroskopische Messungen der Sauerstoff-A-Bande<br />

an Himmelsstreulicht nach der DOAS Methode erlauben die Bestimmung<br />

der Weglängenverteilung solarer Photonen bei ihrem Durchgang<br />

durch die Atmosphäre. Die Messung von Weglängenverteilungen erlaubt<br />

Rückschlüsse über die Statistik der Mehrfachstreuung in Wolken. In<br />

Kombination mit parallel durchgeführten Wolkenradarmessungen und<br />

Mikrowellenradiometermessungen lassen sich besonders Rückschlüsse auf<br />

den atmospherischen Strahlungstransport ziehen.<br />

Ein direkter Hinweis dreidimensionaler Effekte von Wolken auf den<br />

Strahlungstransport ergibt aus der Untersuchung der Beziehung zwischen<br />

den unterschiedlichen Momenten der Photonenweglängenverteilung,

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